ILLUMINA MISEQDX CYSTIC FIBROSIS CLINICAL SEQUENCING ASSAY

{0} 1 # 510(k) SUBSTANTIAL EQUIVALENCE DETERMINATION DECISION SUMMARY A. 510(k) Number: K132750 B. Purpose for Submission: New device C. Measurand: Protein coding regions and intron/exon boundaries of the cystic fibrosis transmembrane conductance gene regulator (CFTR) gene D. Type of Test: High-throughput, Targeted DNA Sequencing E. Applicant: Illumina, Inc. F. Proprietary and Established Names: Illumina MiSeqDx Cystic Fibrosis Clinical Sequencing Assay G. Regulatory Information: 1. Regulation section: 21 CFR 866.5900 CFTR (cystic fibrosis transmembrane conductance regulatory) gene mutation detection system 2. Classification: Class II 3. Product code: PFS, System, Cystic Fibrosis Transmembrane Conductance Regulator Gene, Variant Gene Sequence Detection {1} 4. Panel: Immunology (82) H. Intended Use: 1. Intended use(s): The Illumina MiSeqDx™ Cystic Fibrosis Clinical Sequencing Assay is a targeted sequencing in vitro diagnostic system that re-sequences the protein coding regions and intron/exon boundaries of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene in genomic DNA isolated from human peripheral whole blood specimens collected in K₂EDTA. The test detects single nucleotide variants, and small InDels within the region sequenced, and additionally reports on two deep intronic mutations and two large deletions. The test is intended to be used on the Illumina MiSeqDx Instrument. The test is intended to be used as an aid in the diagnosis of individuals with suspected cystic fibrosis (CF). The test is most appropriate when the patient has an atypical or non-classic presentation of CF or when other mutation panels have failed to identify both causative mutations. The results of the test are intended to be interpreted by a board-certified clinical molecular geneticist or equivalent and should be used in conjunction with other available information including clinical symptoms, other diagnostic tests, and family history. This test is not indicated for use for stand-alone diagnostic purposes, fetal diagnostic testing, for pre-implantation testing, carrier screening, newborn screening, or population screening. 2. Indication(s) for use: Same as intended use 3. Special conditions for use statement(s): For prescription use only 4. Special instrument requirements: Illumina MiSeqDx Instrument using the following software versions: MOS v1.0.27; RTA v1.16.18; MSR v2.2.30; IWM v1.0.14; UMS v1.0.0.5; MTS v1.0.7; Reference Genome File v1.1; Recipe Fragments File v1.0.0; and Manifest File Revision B. I. Device Description: The Illumina MiSeqDx Cystic Fibrosis Clinical Sequencing Assay consists of library preparation and sample indexing reagents, sequencing reagents and consumables, MiSeqDx instrument and data analysis software. A total of 5203 base pairs are sequenced in this assay. The assay additionally reports on the PolyT/PolyTG region in intron 9 and 2 large deletions (CFTRdele2,3 and CFTRdele22,23), bringing the total number of callable positions to 5206. 2 {2} The following is a description of the assay coverage using human genome build 19 (hg19) as the reference sequence. Table 1. Regions of the CFTR gene sequenced by the assay | CFTR Exon | hg19 Genomic coordinate start (chr7) | hg19 Genomic coordinate stop (chr7) | Length (base pair) | | --- | --- | --- | --- | | CFTR_Exon 1 | 117120041 | 117120211 | 171 | | CFTR_Exon 2 | 117144297 | 117144427 | 131 | | CFTR_Exon 3 | 117149078 | 117149206 | 129 | | CFTR_Exon 4 | 117170943 | 117171178 | 236 | | CFTR_Exon 5 | 117174320 | 117174429 | 110 | | CFTR_Exon 6 | 117175292 | 117175475 | 184 | | CFTR_Exon 7^ | 117176597 | 117176737 | 141 | | CFTR_Exon 8 | 117180144 | 117180410 | 267 | | CFTR_Exon 9 | 117182060 | 117182172 | 113 | | CFTR_Exon 10^ | 117188690 | 117188887 | 198 | | CFTR_Exon 11 | 117199508 | 117199719 | 212 | | CFTR_Exon 12 | 117227783 | 117227897 | 115 | | CFTR_Intron 12* | 117229516 | 117229526 | 11 | | CFTR_Exon 13 | 117230397 | 117230503 | 107 | | CFTR_Exon 14 | 117231978 | 117232721 | 744 | | CFTR_Exon 15 | 117234974 | 117235122 | 149 | | CFTR_Exon 16 | 117242870 | 117242927 | 58 | | CFTR_Exon 17 | 117243576 | 117243846 | 271 | | CFTR_Exon 18 | 117246718 | 117246817 | 100 | | CFTR_Exon 19 | 117250563 | 117250733 | 171 | | CFTR_Exon 20 | 117251605 | 117251872 | 268 | | CFTR_Exon 21 | 117254657 | 117254777 | 121 | | CFTR_Exon 22 | 117267566 | 117267834 | 269 | | CFTR_Intron 22* | 117280010 | 117280020 | 11 | | CFTR_Exon 23 | 117282482 | 117282657 | 176 | | CFTR_Exon 24 | 117292886 | 117292995 | 110 | | CFTR_Exon 25 | 117304732 | 117304924 | 193 | | CFTR_Exon 26 | 117305503 | 117305628 | 126 | | CFTR_Exon 27 | 117306952 | 117307262 | 311 | | Total Bases | | | 5203 | ^For Exon 7 and Exon 10, only 5nt of flanking intronic sequence is included upstream of the exon. This is to avoid homopolymeric stretches in these regions. In the case of Exon 10, this is the PolyT/Poly TG region in Intron 9. This region is {3} treated separately. *For the deep intronic mutations, 5 nucleotides flanking the SNV on either side are also included. The assay is designed in a single configuration for 6 runs of 48 samples per kit. The reagent cartridge, flow cell, SBS solution, and filter plates are designed for single use. The assay components are divided into 8 separate boxes, based on amplification stage (pre- or post-amplification) and storage conditions, and include the following components: | | Quantity per kit | Volume | | --- | --- | --- | | Box 1A Pre-Amplification Reagents | | | | CF Clinical Sequencing Assay Oligo Pool | 1 tube | 600 μL | | Hybridization Buffer | 1 tube | 4.32 mL | | Extension-Ligation Mix | 1 tube | 4.8 mL | | Index Primers C (A503), D (A504), and E (A505) | 1 tube per primer | 192 μL | | Index Primers 1 (A701), 2 (A702), and 10 (A710) | 1 tube per primer | 128 μL | | PCR Polymerase | 1 tube | 56 μL | | PCR Master Mix | 1 tube | 2.8 mL | | Box 1B Post-Amp Reagents | | | | Library Normalization Diluent | 1 tube | 4.6 mL | | Library Dilution Buffer | 1 tube | 4.5 mL | | PhiX Internal Control | 1 tube | 10 μL | | Box 2 Post-Amp Reagents | | | | MiSeqDx Reagent Cartridge – CF Clinical Sequencing Assay | 6 cartridges | 1 cartridge | | Box 3A Pre-Amp Reagents | | | | Stringent Wash Buffer | 1 bottle | 24 mL | | Universal Wash Buffer | 1 tube | 4.8 mL | | Box 3B Post-Amp Reagents | | | | PCR Clean-Up Beads | 1 tube | 5 mL | | Library Normalization Wash | 6 tubes | 4.8 mL | | Library Beads | 1 tube | 1.2 mL | | MiSeqDx Flow Cell – CF Clinical Sequencing Assay | 6 containers | 1 flow cell | | Box 4 Post-Amp Reagents | | | | MiSeqDx SBS Solution (PR2) – CF Clinical Sequencing Assay | 6 bottles | 353.1 mL | | Box 5 Pre-Amp Reagents | | | | Filter Plate | 6 plates | N/A | | Box 5 Post-Amp Reagents | | | | Elution Buffer | 1 tube | 4.8 mL | | Library Storage Buffer | 1 tube | 3.5 mL | A brief description of some of the primary components is listed below: - CF Clinical Sequencing Oligo Pools: Oligonucleotides specific for the genomic {4} regions targeted by the test. For each region, there is an upstream locus specific oligonucleotide and a downstream locus specific oligonucleotide - Extension-Ligation Mix: Buffer containing DNA polymerase and DNA ligase, which is applied to the sample on the filter plate and catalyzes the connection of the upstream locus specific oligonucleotide to the downstream locus specific oligonucleotide - PCR Master Mix: Contains all of the components required for PCR amplification except for PCR primers and DNA polymerase - Index PCR Primers: three (3) i7 and three (3) i5 index PCR primers for universal amplification of the ligated products. These primers incorporate P5 and P7 sequences, which are complementary to the sequences of the capture oligonucleotides attached to the flow cell. These primers also incorporate a sample specific sequence tag that is required to pool 8 samples into a single flow cell/MiSeq run. - AMPure XP beads: Streptavidin coated magnetic beads used to capture the PCR product for removal of unincorporated primers and nucleotides. - Library Normalization Diluent/Library Breads: Allow for bead-based normalization of the amount of PCR product produced across different samples. - MiSeq Reagent Cartridge: Pre-filled, single use reagent cartridge which contains the reagents required for cluster generation and SBS sequencing. The pooled libraries are added to the cartridge which is then inserted into the MiSeq instrument. The components of the Reagent Cartridge are as follows: - Incorporation Mix: Contains DNA polymerase, fluorescently labeled nucleotides and buffer used for incorporation of reversible terminator nucleotide during SBS reaction - Scan Mix: Contains buffers to flush out unincorporated fluorescently labeled nucleotides in order to facilitate scanning of the clusters during the SBS reaction - Cleavage Mix: Contains buffers and enzyme that removes the terminator and fluorescent signal from incorporated fluorescently labeled nucleotide, which allows the incorporation of additional nucleotides in later rounds of the SBS reaction - Amplification Mix: Contains buffer, DNA polymerase, and unlabeled nucleotides that are used to bridge amplify the prepared library during the cluster generation process - Amplification Mix for Read 2 - Linearization Pre-mix - Formamide - Linearization Mix 1: Contains enzyme and buffer required to linearize the first read clusters in preparation for their use in the SBS reaction - Linearization Mix 2 - Resynthesis Mix: Contains enzyme and buffer for the synthesis of reads during the cluster generation process - SBS Primer for Read 1 - SBS Primer for Indexing Read - SBS Primer for Read 2 - Water 5 {5} - Flow Cell: Single-use glass substrate with covalently bound oligonucleotides for capture and solid phase amplification and SBS sequencing of the targets created during library preparation # J. Substantial Equivalence Information: 1. Predicate device name(s): Luminex xTAG Cystic Fibrosis 60 Kit v2 2. Predicate $510(\mathrm{k})$ number(s): k083845 3. Comparison with predicate: | Similarities | | | | --- | --- | --- | | Item | New Device MiSeqDx CF Clinical Sequencing Assay | Predicate Luminex xTAG Cystic Fibrosis 60 Kit v2 | | Indication for Use | The test is intended to be used as an aid in the diagnosis of individuals with suspected cystic fibrosis (CF). | Same | | Specimen Type | Genomic DNA isolated from peripheral whole blood | Same | | Anticoagulant | EDTA | EDTA or citrate | | Nucleic Acid Extraction | DNA extraction using validated laboratory method | Same | | Differences | | | | --- | --- | --- | | Item | New Device MiSeqDx CF Clinical Sequencing Assay | Predicate Luminex xTAG Cystic Fibrosis 60 Kit v2 | | Intended Use | The Illumina MiSeqDx(TM) Cystic Fibrosis Clinical Sequencing Assay is a targeted sequencing in vitro diagnostic system that re-sequences the protein coding regions and intron/exon boundaries of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene in genomic DNA isolated | The xTAG® Cystic Fibrosis 60 kit v2 is a device used to simultaneously detect and identify a panel of mutations and variants in the cystic fibrosis transmembrane conductance regulator (CFTR) gene in human blood specimens. The | {6} | Differences | | | | --- | --- | --- | | Item | New Device MiSeqDx CF Clinical Sequencing Assay | Predicate Luminex xTAG Cystic Fibrosis 60 Kit v2 | | | from human peripheral whole blood specimens collected in K2EDTA. The test detects single nucleotide variants, and small InDels within the region sequenced, and additionally reports on two deep intronic mutations and two large deletions. The test is intended to be used on the Illumina MiSeqDx Instrument. The test is intended to be used as an aid in the diagnosis of individuals with suspected cystic fibrosis (CF). The test is most appropriate when the patient has an atypical or non-classic presentation of CF or when other mutation panels have failed to identify both causative mutations. The results of the test are intended to be interpreted by a board-certified clinical molecular geneticist or equivalent and should be used in conjunction with other available information including clinical symptoms, other diagnostic tests, and family history. | panel includes mutations and variants currently recommended by the American College of Medical Genetics and American College of Obstetricians and Gynecologists (ACMG/ACOG) plus some of the world’s most common and North American prevalent mutations. The xTAG Cystic Fibrosis 60 kit v2 is a qualitative genotyping test which provides information intended to be used for carrier testing in adults of reproductive age, as an aid in newborn screening, and in confirmatory diagnostic testing in newborns and children. | | Uses for which the Test is Not Indicated | Not indicated for stand-alone diagnostic purposes, fetal diagnostic testing, for pre-implantation testing, carrier screening, newborn screening, or population screening | Not indicated for fetal diagnostic testing, pre-implantation testing, or for stand-alone diagnostic purposes | | Interpretation of Results | Intended to be interpreted by a board-certified clinical molecular geneticist or equivalent | Specialized interpretation not required | | Assay Type | High-throughput targeted amplicon-based sequencing | Qualitative nucleic acid multiplex test | | Variants Detected | Single nucleotide variants and small indels (<3 bp) from the protein coding regions and | 60 CFTR mutations and 4 variants (benign polymorphisms) | {7} | Differences | | | | --- | --- | --- | | Item | New Device MiSeqDx CF Clinical Sequencing Assay | Predicate Luminex xTAG Cystic Fibrosis 60 Kit v2 | | | intron/exon boundaries of the CFTR gene, including two deep intronic mutations and two large deletions | | | Technology | High-throughput, Targeted DNA Sequencing, Sequencing by Synthesis (SBS). Reversible terminator-based method to detect single bases as they are incorporated into growing DNA strands. Fluorescently-labeled terminators are detected using a dual-color laser. Base calls are made directly from signal intensity measurements during each sequencing cycle. | Multiplex PCR followed by multiplex allele specific primer extension for genotyping, hybridized to multiplex fluorescent microparticles, and run on fluidic microbead reader which includes a dual-color laser detection system that enables optical scanning by flow cytometry. | | Instrument System | MiSeqDx | Luminex 100 or 200 IS | # K. Standard/Guidance Document Referenced (if applicable): Guidance for Industry and FDA Staff: Class II Special Controls Guidance Document: CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) Gene Mutation Detection Systems; October 26, 2005 Guidance for Industry and FDA Staff: Guidance for the Content of Premarket Submissions for Software Contained in Medical Devices; May 11, 2005 General Principles of Software Validation; Final Guidance for Industry and FDA Staff; January 11, 2002 Guidance for Industry - Cybersecurity for Networked Medical Devices Containing Off-the-Shelf (OTS) Software; January 14, 2005 Guidance for Industry, FDA Reviewers and Compliance on Off-the-Shelf Software Use in Medical Devices; September 9, 1999 CLSI Standard EP05-A2, Evaluation of Precision Performance of Quantitative Measurement Methods; Approved Guideline – Second Edition. CLSI Standard EP07-A3, Interference Testing in Clinical Chemistry, Approved Guideline – Third Edition. {8} CLSI Standard EP09-A2, Method Comparison and Bias Estimation Using Patient Samples, Approved Guideline – Second Edition. CLSI Standard EP12-A2, User Protocol for Evaluation of Qualitative Test Performance; Approved Guideline – Second Edition. CLSI Standard EP14-A2, Evaluation of Matrix Effects, Approved Guideline – Second Edition. CLSI Standard EP17-A, Protocols for the Determination of Limits of Detection and Limits of Quantification, Approved Guideline. CLSI Standard EP25-A, Evaluation of Stability on In Vitro Diagnostic Reagents, Approved Guideline. L. Test Principle: The Illumina MiSeqDx Cystic Fibrosis Clinical Sequencing Assay encompasses two main procedures. The first is to manually prepare the samples for sequencing, which is called library preparation. Library preparation consists of four key steps: Hybridization, Extension-Ligation, PCR Amplification, and Library Normalization. The first step, Hybridization, hybridizes a pool of upstream and downstream oligonucleotides specific to the MiSeqDx Cystic Fibrosis Clinical Sequencing Assay to the sample genomic DNA. At the end of this process a three-step wash procedure with a filter capable of size selection removes unbound oligonucleotides from the genomic DNA. The second step, Extension-Ligation, connects the hybridized upstream and downstream oligonucleotides. A DNA polymerase extends from the upstream oligonucleotides through the targeted region, followed by ligation to the 5′ end of the downstream oligonucleotide using a DNA ligase. The result is the formation of products that contain the CF specific oligonucleotides flanked by sequences required for amplification. The third step, PCR Amplification, amplifies the extension-ligated products using primers that add index sequences for sample multiplexing, as well as common adapters required for cluster generation on the MiSeqDx. At the end of this process, a PCR clean-up procedure purifies the PCR products (referred to as a library). The final step, Library Normalization, normalizes the quantity of each library to ensure more equal library representation in the final pooled library. At the end of this process, the pooled library is loaded onto the MiSeqDx for sequencing by Sequencing by Synthesis (SBS) chemistry. The second procedure is to sequence the prepared samples using SBS chemistry on the MiSeqDx. SBS chemistry uses a reversible-terminator method to detect single nucleotide bases as they are incorporated into growing DNA strands. During each sequencing cycle, a single fluorescently labeled deoxynucleotide triphosphate (dNTP) is added to the nucleic acid chain. The nucleotide label serves as a terminator for polymerization, so after each dNTP incorporation, the fluorescent dye is imaged to identify the base and then enzymatically cleaved to allow incorporation of the next nucleotide. Because all four reversible terminator-bound dNTPs (A, G, T, C) are present as single, separate molecules, natural competition minimizes incorporation bias. Base calls are made directly from signal intensity measurements during each sequencing cycle. The end result is base-by-base sequencing. 9 {9} The MiSeq Reporter software processes base calls generated during primary analysis and produces information about each sample based on information specified in the samples sheet, called secondary analysis. As described below, secondary analysis includes de-multiplexing, FASTQ file generation, alignment, variant calling, and generation of VCF files containing information about CFTR variants found at specific positions. De-multiplexing separates data from pooled samples based upon the unique sequence indexes that were added during the PCR amplification step. The FASTQ format is a text format used to represent sequences. FASTQ files contain the reads for each sample and the quality scores, excluding reads from any clusters that did not pass filter. Alignment compares sequences against the reference to identify a relationship between the sequences and assigns a score based on regions of similarity. Aligned reads are written to files in BAM format. MiSeq Reporter software uses a banded Smith-Waterman algorithm that performs local sequence alignments to determine similar regions between two sequences. Variant calling then records insertion and deletions (indels), and other structural variants in a standardized and parsable test file. ## M. Performance Characteristics (if/when applicable): ### 1. Analytical performance: #### a. Precision/Reproducibility: **Reproducibility:** The reproducibility of the MiSeqDx assay was evaluated at 3 external sites, by two operators at each site on 3 nonconsecutive days. The study included 2 sample panels consisting of mock blood and genomic DNA (gDNA) samples. The mock blood samples were created from leukocyte-depleted whole blood spiked with cell lines known to harbor a CFTR mutation. The gDNA samples were derived from cell lines with known CFTR variants. Panel A was comprised of 8 mock blood samples and 38 gDNA samples. Panel B was comprised of 38 gDNA samples. A new sample library was prepared for each run. A total of 18 runs per panel were performed. There were 16 duplicate samples between the 2 panels, giving a total of 76 unique samples of the total 92. Positive and negative control samples were included in each run. A positive percent agreement (PPA), negative percent agreement (NPA), and overall agreement (OA) were assessed. Sanger sequencing was used to identify the variants with the exception of the 2 large deletions that were verified using a validated PCR assay followed by sequencing of the resulting amplicons. There were 7 runs identified as invalid due to failed QC metrics and were re-run. Additionally, 5 samples failed QC metrics. These samples were not run again and results from these samples were considered non-matches at every position. Two of the samples had a 0% call rate, which upon further investigation, it was determined that the samples were not added when making up the library preparation. For the remaining samples, there were 63 discordant results between the assay and Sanger 10 {10} sequencing along the 5206 callable positions. Of these 39 were due to a no call by the assay. Of the remaining 24 discordant calls, 18 occurred in sample 80 and were for the PolyTG/PolyT region. The remaining 6 discordant results were miscalls occurring in a single run (i.e., disagreed with calls reported by the other 17 runs). Overall, the study achieved a genotype-level PPA of $99.2\%$ , NPA of $99.7\%$ , and OA of $99.7\%$ which met all of the acceptance criteria for the study. Table 2 below represents the summary reproducibility results for observed variants, excluding the PolyTG/PolyT region, while the Table 3 summarizes the PolyTG/PolyT results. PPA, NPA, and OA were determined for all 5206 callable positions. However the variants observed are shown below for simplicity and because the majority of discordant results were in the context of variant detection, most notably in the PolyTG/PolyT region. Table 2: Reproducibility for Variants Observed in Sample Panel | Sample | HGVS Name (or Location if no HGVS) | Variant Name | Total Results | | Agreeing Calls | | | Total # (All Sites) | | OA (%) | | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | | | | | Per Site | All Sites | Site 1 | Site 2 | Site 3 | No Calls* | Miscalls | | | 1 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 1 | c.1646G>A | S549N | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 1 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 2 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 2 | c.1581A>G | E527E | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 2 | c.1680-1G>A | 1812-1 G>A | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 2 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 2 | c.312delA | 444delA | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 2 | c.3870A>G | P1290P | 6 | 18 | 6 | 5 | 6 | 0 | 1 | 94.44 | | 2 | c.4389G>A | Q1463Q | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 3 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 3 | c.1477C>T | Q493X | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 3 | c.1521_1523delCTT | F508del | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 3 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 3 | c.4389G>A | Q1463Q | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 4 | c.1408G>A | V470M | 6 | 18 | 5 | 6 | 6 | 1 | 0 | 94.44 | | 4 | c.1521_1523delCTT | F508del | 6 | 18 | 5 | 6 | 6 | 1 | 0 | 94.44 | | 4 | c.2052delA | 2184delA | 6 | 18 | 5 | 6 | 6 | 1 | 0 | 94.44 | | 5 | c.1408G>A | V470M | 6 | 18 | 6 | 5 | 6 | 1¶ | 0 | 94.44 | | 5 | c.224G>A | R75Q | 6 | 18 | 6 | 5 | 6 | 1¶ | 0 | 94.44 | | 5 | c.2562T>G | T854T | 6 | 18 | 6 | 5 | 6 | 1¶ | 0 | 94.44 | | 5 | c.3472C>T | R1158X | 6 | 18 | 6 | 5 | 6 | 1¶ | 0 | 94.44 | | 5 | c.366T>A | Y122X | 6 | 18 | 6 | 5 | 6 | 1¶ | 0 | 94.44 | {11} | Sample | HGVS Name (or Location if no HGVS) | Variant Name | Total Results | | Agreeing Calls | | | Total # (All Sites) | | OA (%) | | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | | | | | Per Site | All Sites | Site 1 | Site 2 | Site 3 | No Calls* | Miscalls | | | 5 | c.625G>T | A209S | 6 | 18 | 6 | 5 | 6 | 1# | 0 | 94.44 | | 6 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 6 | c.1521_1523delCTT | F508del | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 6 | c.2051_2052delAAins G | 2183AA>G | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 7 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 7 | c.223C>T | R75X | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 7 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 8 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 8 | c.1519_1521delATC | I507del | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 8 | c.1521_1523delCTT | F508del | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 8 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 8 | c.4389G>A | Q1463Q | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 9 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 9 | c.1521_1523delCTT | F508del | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 9 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 9 | c.3846G>A | W1282X | 6 | 18 | 6 | 5 | 6 | 0 | 1# | 94.44 | | 9 | c.4389G>A | Q1463Q | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 10 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 10 | c.1521_1523delCTT | F508del | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 10 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 10 | c.3140-26A>G | 3272-26A>G | 6 | 18 | 6 | 5 | 6 | 0 | 1# | 94.44 | | 10 | c.4389G>A | Q1463Q | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 11, 39 | c.1408G>A | V470M | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 11, 39 | c.1521_1523delCTT | F508del | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 11, 39 | c.2002C>T | R668C | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 11, 39 | c.2562T>G | T854T | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 11, 39 | c.3717+12191C>T | 3849+10kbC>T | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 11, 39 | c.4389G>A | Q1463Q | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 12, 40 | c.1408G>A | V470M | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 12, 40 | c.2562T>G | T854T | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 12, 40 | c.2988+1G>A | 3120+1G>A | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 12, 40 | c.4389G>A | Q1463Q | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 12, 40 | c.489+1G>T | 621+1G>T | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 13 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 13 | c.1521_1523delCTT | F508del | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 13 | c.178G>T | E60X | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 13 | c.4389G>A | Q1463Q | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 14 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | {12} | Sample | HGVS Name (or Location if no HGVS) | Variant Name | Total Results | | Agreeing Calls | | | Total # (All Sites) | | OA (%) | | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | | | | | Per Site | All Sites | Site 1 | Site 2 | Site 3 | No Calls* | Miscalls | | | 14 | c.1584G>A | E528E | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 14 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 14 | c.3302T>A | M1101K | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 15 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 15 | c.1584G>A | E528E | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 15 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 15 | c.3302T>A | M1101K | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 16 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 16 | c.1521_1523delCTT | F508del | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 16 | c.3080T>C | I1027T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 17, 41 | c.1408G>A | V470M | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 17, 41 | c.1521_1523delCTT | F508del | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 17, 41 | c.3528delC | 3659delC | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 18, 42 | 117120145 | 117120145 | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 18, 42 | c.1408G>A | V470M | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 18, 42 | c.1521_1523delCTT | F508del | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 18, 42 | c.350G>A | R117H | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 19 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 19 | c.489+1G>T | 621+1G>T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 19 | c.579+1G>T | 711+1G>T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 20, 43 | c.1408G>A | V470M | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 20, 43 | c.254G>A | G85E | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 20, 43 | c.489+1G>T | 621+1G>T | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 21, 44 | c.1364C>A | A455E | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 21, 44 | c.1408G>A | V470M | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 21, 44 | c.1521_1523delCTT | F508del | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 22 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 22 | c.1521_1523delCTT | F508del | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 22 | c.1679G>C | R560T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 22 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 22 | c.4389G>A | Q1463Q | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 23 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 23 | c.1521_1523delCTT | F508del | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 23 | c.3276C>A | Y1092X (C>A) | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 24, 45 | c.1408G>A | V470M | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 24, 45 | c.3909C>G | N1303K | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 24, 45 | c.4046G>A | G1349D | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 25 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 25 | c.1624G>T | G542X | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | {13} | Sample | HGVS Name (or Location if no HGVS) | Variant Name | Total Results | | Agreeing Calls | | | Total # (All Sites) | | OA (%) | | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | | | | | Per Site | All Sites | Site 1 | Site 2 | Site 3 | No Calls* | Miscalls | | | 26 | 117120141 | 117120141 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 26 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 26 | c.1624G>T | G542X | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 27, 46 | c.1408G>A | V470M | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 27, 46 | c.1652G>A | G551D | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 27, 46 | c.1657C>T | R553X | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 27, 46 | c.2562T>G | T854T | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 27, 46 | c.4389G>A | Q1463Q | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 28 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 28 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 28 | c.3717+12191C>T | 3849+10kbC>T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 28 | c.4389G>A | Q1463Q | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 29 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 29 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 29 | c.91C>T | R31C | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 30 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 30 | c.1521_1523delCTT | F508del | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 30 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 30 | c.3485G>T | R1162L | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 30 | c.4389G>A | Q1463Q | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 31 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 31 | c.1585-1G>A | 1717-1G>A | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 31 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 31 | c.4389G>A | Q1463Q | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 32 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 32 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 32 | c.3484C>T | R1162X | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 32 | c.4389G>A | Q1463Q | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 33 | c.1040G>C | R347P | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 33 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 33 | c.1652G>A | G551D | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 33 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 33 | c.4272C>T | Y1424Y | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 33 | c.4389G>A | Q1463Q | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 34 | c.1000C>T | R334W | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 34 | c.3368-2A>T | c.3368-2A>T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 35 | c.1523T>G | F508C | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 36 | c.254G>A | G85E | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 36 | c.3454G>C | D1152H | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | {14} | Sample | HGVS Name (or Location if no HGVS) | Variant Name | Total Results | | Agreeing Calls | | | Total # (All Sites) | | OA (%) | | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | | | | | Per Site | All Sites | Site 1 | Site 2 | Site 3 | No Calls* | Miscalls | | | 37 | c.1007T>A | I336K | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 37 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 37 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 37 | c.3705T>G | S1235R | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 38 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 38 | c.1727G>C | G576A | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 38 | c.2002C>T | R668C | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 38 | c.2057C>A | S686Y | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 38 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 38 | c.4389G>A | Q1463Q | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 47, 85 | c.1408G>A | V470M | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 47, 85 | c.2562T>G | T854T | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 47, 85 | c.2657+5G>A | 2789+5G>A | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 47, 85 | c.4389G>A | Q1463Q | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 48, 86 | c.54-5940_273+10250del21kb | CFTRdele2,3 | 12 | 36 | 12 | 11 | 12 | 1 | 0 | 97.22 | | 48, 86 | c.1408G>A | V470M | 12 | 36 | 12 | 11 | 12 | 1 | 0 | 97.22 | | 48, 86 | c.1521_1523delCTT | F508del | 12 | 36 | 12 | 11 | 12 | 1 | 0 | 97.22 | | 49, 87 | c.1408G>A | V470M | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 49, 87 | c.1521_1523delCTT | F508del | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 49, 87 | c.1766+1G>A | 1898+1G>A | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 50, 88 | c.1408G>A | V470M | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 50, 88 | c.220C>T | R74W | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 50, 88 | c.2562T>G | T854T | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 50, 88 | c.3808G>A | D1270N | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 51, 89 | c.1408G>A | V470M | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 51, 89 | c.1521_1523delCTT | F508del | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 51, 89 | c.2012delT | 2143delT | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 52 | c.3744delA | 3876delA | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 53, 90 | c.3773_3774insT | 3905insT | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 54, 91 | c.1408G>A | V470M | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 54, 91 | c.262_263delTT | 394delTT | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 55, 92 | c.1408G>A | V470M | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 55, 92 | c.1519A>G | I507V | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 55, 92 | c.1521_1523delCTT | F508del | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 55, 92 | c.2562T>G | T854T | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 55, 92 | c.3080T>C | I1027T | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 55, 92 | c.4389G>A | Q1463Q | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100 | | 56 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | {15} | Sample | HGVS Name (or Location if no HGVS) | Variant Name | Total Results | | Agreeing Calls | | | Total # (All Sites) | | OA (%) | | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | | | | | Per Site | All Sites | Site 1 | Site 2 | Site 3 | No Calls* | Miscalls | | | 56 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 56 | c.3154T>G | F1052V | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 56 | c.4389G>A | Q1463Q | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 57 | 117120141 | 117120141 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 57 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 57 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 57 | c.3209G>A | R1070Q | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 58 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 58 | c.1521_1523delCTT | F508del | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 58 | c.2991G>C | L997F | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 59 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 59 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 59 | c.3205G>A | G1069R | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 60 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 60 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 60 | c.4389G>A | Q1463Q | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 60 | c.617T>G | L206W | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 61 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 61 | c.2260G>A | V754M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 61 | c.4389G>A | Q1463Q | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 62 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 62 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 62 | c.988G>T | G330X | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 64 | c.1040G>A | R347H | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 64 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 64 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 64 | c.4389G>A | Q1463Q | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 65 | c.948delT | 1078delT | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 66 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 66 | c.1521_1523delCTT | F508del | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 66 | c.532G>A | G178R | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 67 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 67 | c.1647T>G | S549R (c.1647T>G) | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 68 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 68 | c.1646G>A | S549N | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 68 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 68 | c.4389G>A | Q1463Q | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 69 | c.2506G>T | D836Y | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | {16} | Sample | HGVS Name (or Location if no HGVS) | Variant Name | Total Results | | Agreeing Calls | | | Total # (All Sites) | | OA (%) | | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | | | | | Per Site | All Sites | Site 1 | Site 2 | Site 3 | No Calls* | Miscalls | | | 69 | c.2537G>A | W846X | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 70 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 70 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 70 | c.3485G>T | R1162L | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 70 | c.4389G>A | Q1463Q | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 71 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 71 | c.1521_1523delCTT | F508del | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 71 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 71 | c.274G>T | E92X | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 71 | c.4389G>A | Q1463Q | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 72 | c.1022_1023insTC | 1154insTC | 6 | 18 | 6 | 6 | 5 | 1 | 0 | 94.44 | | 72 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 5 | 1 | 0 | 94.44 | | 72 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 5 | 1 | 0 | 94.44 | | 72 | c.4389G>A | Q1463Q | 6 | 18 | 6 | 6 | 5 | 1 | 0 | 94.44 | | 72 | c.489+1G>T | 621+1G>T | 6 | 18 | 6 | 6 | 5 | 1 | 0 | 94.44 | | 73 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 73 | c.1624G>T | G542X | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 73 | c.1826A>G | H609R | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 74 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 5 | 0 | 1 | 94.44 | | 74 | c.1429C>T | P477S | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 74 | c.1521_1523delCTT | F508del | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 75 | c.1408G>A | V470M | 6 | 18 | 6 | 5 | 6 | 1* | 0 | 94.44 | | 75 | c.1521_1523delCTT | F508del | 6 | 18 | 6 | 5 | 6 | 1* | 0 | 94.44 | | 75 | c.1721C>A | P574H | 6 | 18 | 6 | 5 | 6 | 1* | 0 | 94.44 | | 76 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 76 | c.1521_1523delCTT | F508del | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 76 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 76 | c.425delT | F143LfsX10 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 76 | c.4389G>A | Q1463Q | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 77 | c.1364C>A | A455E | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 77 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 77 | c.489+1G>T | 621+1G>T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 78 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 78 | c.1581A>G | E527E | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 78 | c.1680-1G>A | 1812-1 G>A | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 78 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 78 | c.312delA | 444delA | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 78 | c.3870A>G | P1290P | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | {17} | Sample | HGVS Name (or Location if no HGVS) | Variant Name | Total Results | | Agreeing Calls | | | Total # (All Sites) | | OA (%) | | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | | | | | Per Site | All Sites | Site 1 | Site 2 | Site 3 | No Calls* | Miscalls | | | 78 | c.4389G>A | Q1463Q | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 79 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 79 | c.220C>T | R74W | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 79 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 79 | c.3808G>A | D1270N | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 80 | 117120141 | 117120141 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 80 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 80 | c.1521_1523delCTT | F508del | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 80 | c.1657C>T | R553X | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 80 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 81 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 81 | c.1521_1523delCTT | F508del | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 81 | c.1652G>A | G551D | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 81 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 81 | c.4389G>A | Q1463Q | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 82 | c.1040G>C | R347P | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 82 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 82 | c.1521_1523delCTT | F508del | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 82 | c.4272C>T | Y1424Y | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 83 | 11720145 | 11720145 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 83 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 83 | c.1521_1523delCTT | F508del | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 83 | c.350G>A | R117H | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 84 | c.1408G>A | V470M | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 84 | c.1519_1521delATC | I507del | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 84 | c.2562T>G | T854T | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | 84 | c.4389G>A | Q1463Q | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100 | | Total All Variants (PPA)* | | | 2580 | 7740 | 2562 | 2553 | 2565 | 37 | 23 | 99.22 | | Total All WT (NPA) | | | 2871132 | 8613396 | 2865930 | 2855526 | 2865932 | 26006 | 2 | 99.70 | | Total All WT and variants (OA) | | | 2873712 | 8621136 | 2868492 | 2858079 | 2868497 | 26043 | 25 | 99.70 | *Samples were not retested. One replicate each of samples 5 and 75 had a $0\%$ call rate. Further investigation indicated that the samples had likely not been added to the sample plate prior to library preparation. Upon review, samples 9 and 10 were likely switched by the operator prior to library preparation. * Excluding PolyTG/PolyT variants, the PA was 99.60% a Covers all 5206 callable positions interrogated by the assay The panels used for the reproducibility studies included a number of PolyTG/PolyT tract variations that allowed for examination of assay performance over the majority of permutations in tract size. With the exception of (TG)11(T)7/(TG)11(T)9 samples, {18} the assay performed similarly regardless of PolyTG/PolyT tract size. The table below outlines reproducibility results by PolyTG/PolyT tract size. Table 3: Reproducibility for PolyTG/PolyT Variants Observed in Sample Panel | Panel | Sample | Genotype | Test Results | | Agreeing Calls | | | Total (All Sites) | | % Agreement | | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | | | | | Per Site | All Sites | Site 1 | Site 2 | Site 3 | No Calls | Miscalls | | | A | 1 | (TG)12(T)7/(TG)12(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | A | 2 | (TG)10(T)9/(TG)10(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | A | 3 | (TG)10(T)7/(TG)10(T)9 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | A | 4 | (TG)10(T)9/(TG)11(T)7 | 6 | 18 | 5 | 6 | 6 | 1 | 0 | 94.44% | | A | 5 | (TG)10(T)7/(TG)11(T)7 | 6 | 18 | 6 | 5 | 6 | 1 | 0 | 94.44% | | A | 6 | (TG)10(T)9/(TG)10(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | A | 7 | (TG)10(T)9/(TG)11(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | A | 8 | (TG)10(T)7/(TG)10(T)9 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | A | 9 | (TG)10(T)9/(TG)10(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | A | 10 | (TG)10(T)9/(TG)10(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | A | 11, 39 | (TG)10(T)9/(TG)10(T)7 | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100% | | A | 12, 40 | (TG)10(T)9/(TG)11(T)7 | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100% | | A | 13 | (TG)10(T)9/(TG)11(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | A | 14 | (TG)10(T)7/(TG)11(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | A | 15 | (TG)10(T)7/(TG)11(T)7 | 6 | 18 | 6 | 5 | 6 | 1 | 0 | 94.44% | | A | 16 | (TG)10(T)9/(TG)10(T)9 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | A | 17, 41 | (TG)10(T)9/(TG)11(T)7 | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100% | | A | 18, 42 | (TG)10(T)9/(TG)12(T)5 | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100% | | A | 19 | (TG)10(T)9/(TG)11(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | A | 20, 43 | (TG)10(T)9/(TG)11(T)7 | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100% | | A | 21, 44 | (TG)10(T)9/(TG)10(T)9 | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100% | | A | 22 | (TG)10(T)9/(TG)10(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | A | 23 | (TG)10(T)9/(TG)11(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | A | 24, 45 | (TG)10(T)9/(TG)11(T)7 | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100% | | A | 25 | (TG)10(T)9/(TG)10(T)9 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | A | 26 | (TG)10(T)9/(TG)11(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | {19} | A | 27,46 | (TG)10(T)7/(TG)11(T)7 | 12 | 36 | 11 | 12 | 12 | 0 | 1 | 97.22% | | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | | A | 28 | (TG)10(T)7/(TG)10(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | A | 29 | (TG)10(T)7/(TG)12(T)7 | 6 | 18 | 6 | 4 | 4 | 4 | 0 | 77.78% | | A | 30 | (TG)10(T)9/(TG)10(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | A | 31 | (TG)10(T)7/(TG)11(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | A | 32 | (TG)10(T)7/(TG)10(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | A | 33 | (TG)10(T)7/(TG)11(T)7 | 6 | 18 | 5 | 6 | 6 | 1 | 0 | 94.44% | | A | 34 | (TG)11(T)7/(TG)12(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | A | 35 | (TG)11(T)7/(TG)11(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | A | 36 | (TG)11(T)7/(TG)11(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | A | 37 | (TG)11(T)7/(TG)12(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | A | 38 | (TG)10(T)7/(TG)11(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | B | 47,85 | (TG)10(T)7/(TG)10(T)7 | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100% | | B | 48,86 | (TG)10(T)9/(TG)11(T)7 | 12 | 36 | 11 | 11 | 12 | 2 | 0 | 94.44% | | B | 49,87 | (TG)10(T)9/(TG)11(T)7 | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100% | | B | 50,88 | (TG)10(T)9/(TG)11(T)7 | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100% | | B | 51,89 | (TG)10(T)9/(TG)10(T)9 | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100% | | B | 52 | (TG)11(T)7/(TG)11(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | B | 53,90 | (TG)11(T)7/(TG)11(T)7 | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100% | | B | 54,91 | (TG)10(T)9/(TG)11(T)7 | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100% | | B | 55,92 | (TG)10(T)9/(TG)10(T)7 | 12 | 36 | 12 | 12 | 12 | 0 | 0 | 100% | | B | 56 | (TG)10(T)7/(TG)10(T)9 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | B | 57 | (TG)12(T)7/(TG)12(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | B | 58 | (TG)10(T)9/(TG)10(T)9 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | B | 59 | (TG)11(T)7/(TG)12(T)7 | 6 | 18 | 5 | 6 | 6 | 1 | 0 | 94.44% | | B | 60 | (TG)9(T)9/(TG)11(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | B | 61 | (TG)10(T)9/(TG)11(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | B | 62 | (TG)10(T)7/(TG)11(T)7 | 6 | 18 | 5 | 6 | 6 | 1 | 0 | 94.44% | | B | 63 | (TG)11(T)7/(TG)11(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | B | 64 | (TG)10(T)7/(TG)11(T)7 | 6 | 18 | 5 | 6 | 6 | 1 | 0 | 94.44% | {20} | B | 65 | (TG)11(T)7/(TG)11(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | | B | 66 | (TG)10(T)9/(TG)11(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | B | 67 | (TG)11(T)7/(TG)11(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | B | 68 | (TG)10(T)7/(TG)11(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | B | 69 | (TG)11(T)7/(TG)11(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | B | 70 | (TG)10(T)7/(TG)10(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | B | 71 | (TG)10(T)9/(TG)11(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | B | 72 | (TG)10(T)7/(TG)10(T)9 | 6 | 18 | 5 | 6 | 5 | 2 | 0 | 88.89% | | B | 73 | (TG)10(T)9/(TG)11(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | B | 74 | (TG)10(T)9/(TG)11(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | B | 75 | (TG)10(T)7/(TG)10(T)9 | 6 | 18 | 6 | 5 | 6 | 1 | 0 | 94.44% | | B | 76 | (TG)10(T)7/(TG)10(T)9 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | B | 77 | (TG)10(T)9/(TG)10(T)9 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | B | 78 | (TG)10(T)7/(TG)10(T)9 | 6 | 18 | 5 | 6 | 6 | 1 | 0 | 94.44% | | B | 79 | (TG)10(T)7/(TG)11(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | B | 80 | (TG)11(T)7/(TG)11(T)9 | 6 | 18 | 0 | 0 | 0 | 0 | 18†† | 0% | | B | 81 | (TG)10(T)7/(TG)10(T)9 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | B | 82 | (TG)10(T)9/(TG)11(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | B | 83 | (TG)10(T)9/(TG)12(T)5 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | B | 84 | (TG)10(T)7/(TG)10(T)7 | 6 | 18 | 6 | 6 | 6 | 0 | 0 | 100% | | Total PolyTG/PolyT Variants (PA) | | | 552 | 1656 | 537 | 540 | 543 | 17 | 19 | 97.83% | †† All 18 samples were concordant with each other but discordant with Sanger bi-directional sequencing. # Lot-to-Lot Reproducibility: A single operator performed a lot-to-lot reproducibility study using the three kit lots and one instrument. Each kit lot included all the reagents and materials intended to be packaged as part of the Illumina MiSeqDx Cystic Fibrosis Clinical Sequencing Assay. A panel of 47 unique gDNA samples tested in duplicate was tested on each lot. The samples were selected to represent a wide array of potential variants. Samples were extracted from immortalized cell lines and included the ACMG 23 mutations, 21 deletion/insertion variants, 5 homozygous samples, 28 compound heterozygotes, 1 sample containing 1 of the large deletions, samples which represent the commonly observed sequence possibilities at the PolyTG/Poly T region, and single nucleotide polymorphisms (SNPs) in 15 {21} different exons and 9 different intronic regions. There were no miscalls. There were 5 no calls for lot 1, 1 no call for lot 2 and 0 no calls for lot 3. Results showed that all reagent lots met their acceptance criteria and performed equivalently. ## Instrument-to-Instrument Reproducibility: To establish instrument comparability, assay performance (call rate, reproducibility, sample first pass rate, and accuracy) was assessed on 3 different MiSeqDx instruments. Three operators each performed a single run on 3 different days on each of 3 different MiSeqDx instruments using a single lot of reagents. Instrument performance metrics were defined by sequencing output (in gigabases), reads (in millions), read length (2x150), and quality base calling score $(\% \mathrm{Q}) &gt; 30$. The 48 sample panel used in the lot-to-lot reproducibility study (47 samples plus a no-template control [NTC]) which represented different types of sequence variations was used in this study. If a NTC generated a call rate of $&lt;2\%$, then contamination would be suspected and the entire sequencing run would be considered failed and must be repeated starting from library preparation. The Clinical Sequencing Assay sequences 5203 bases within the exonic regions and flanking intronic sequence and additionally reports on 2 large deletions and the PolyTG/PolyT sequence within intron 9, making the total number of positions sequences 5,206. With the exception of a single sample which had a no-call at a PolyTG/PolyT site, all 423 tests (47 samples x 9runs [3 operators x 3 instruments]) had a $100\%$ call rate and reproducibility was $100\%$ concordant. Accuracy examination by bi-directional sequencing also showed all samples had the expected sequence/genotype. ## Thermal Cycler Evaluation: Three different commonly used, commercially available thermal cyclers were compared for use in library preparation for the MiSeqDx Cystic Fibrosis Clinical Sequencing Assay. Three unique sample sets were processed through the 3 thermal cyclers across 3 days. Each sample set was processed in triplicate each day (one replicate per thermal cycler). The sample set consisted of 15 extracted gDNAs from cell lines and 1 NTC. The sample panel included variants for every allele of the ACMG 23, 21 deletion/insertion variants, 5 homozygous samples, 27 compound heterozygotes, 1 sample containing one of the targeted large deletions, samples with commonly observed variants in the Poly TG/PolyT region and SNPs in 15 different exons and 9 different intronic regions. The data for each thermal cycler met specifications for call rate, accuracy and sample first pass rate. 22 {22} 23 # DNA Extraction Study: To evaluate the effect of the extraction step on sample reproducibility, an additional, separate extraction study was conducted. Three different commonly used DNA extraction methods from K₂EDTA anticoagulated whole blood were tested on 14 blood samples (2 samples were wild-type, while the other 12 represented 8 unique genotypes). The genomic DNA was isolated using three commonly used commercially available kits representing different methodologies (i.e., magnetic bead separation, alcohol precipitation, and silica filter column). The 3 DNA extraction methods were tested by 2 different operators who performed 3 runs per extraction method giving 9 replicate extractions per sample performed on separate days. All extracted gDNA samples were run in duplicate. All 3 extraction methods met acceptance criteria for call rate, reproducibility, and pass rate with an accuracy of 100%. ## Repeatability: To examine assay repeatability, 47 replicates of a single sample (with a NTC) were tested. The same experiment was repeated for a second sample by the same operator on the same instrument. The percent coefficient of variation (% CV) for coverage was determined for each of the 80 amplicons examined in this assay across 47 replicates. Results ranged from 7-18% CV with an average of 12% for sample 1 and 12% for sample 2. ## b. Linearity/Assay Reportable range: Not applicable. ## c. Traceability, Stability, Expected values (controls, calibrators, or methods): ### Real-Time Stability: In order to determine the expiration dating of the MiSeqDx Cystic Fibrosis Clinical Sequencing Assay reagents and consumables, the kit was evaluated at six time points after manufacturing: 5 months, 6.25 months, 7.25 months, 9 months, 9.25 months, and 12 months with three separately manufactured lots of reagents and consumables. Each lot of reagents was run in duplicate for the first 3 time points and singlicate at the 9 month time point. A panel of 45 specimens was used to assess performance. The results from each lot at each time point was assessed for call rate (acceptance criteria ≥99%), and accuracy (acceptance criteria ≥99.9%). No miscalls were observed for any of the time points. The largest number of no calls (N = 5) was observed with one lot at 7.25 months; however the call rate exceeded the acceptance criteria. All No Calls observed at any time point were for the PolyTG/PolyT variant. Based on the data provided, the initial shelf-life for the assay is 9.25 months. {23} 24 # Open Tube Stability (Freeze/Thaw): Three independently manufactured lots of frozen library preparation/normalization reagents were used for testing. The assay reagents are single use and not stored frozen, and so were not tested in this protocol. All reagents were subjected to 6 freeze/thaw cycles. At each cycle (1 per day for 6 days), reagents were thawed at room temperature, the reagent volume required for testing was withdrawn, and the tubes were returned to -15 to -25°C for overnight storage. Thirteen gDNA samples were tested, including 1 NTC for a total of 14 samples. The 14 samples were pooled into a single library at each freeze/thaw time point and sequencing was run in the assay mode. Each freeze/thaw cycle was assessed for first pass rate (acceptance criteria ≥95% samples need to meet sample call rate specification of ≥99%), call rate (acceptance criteria ≥99%), and accuracy (acceptance criteria ≥99.9%). The data provided supports a maximum of 6 rounds of freeze/thaw. # Specimen Sampling and Handling: The specimen handling study included the following conditions: - DNA extracted from K₂EDTA anti-coagulated blood stored at room temperature (20-25°C) for 7 days (claimed in package insert) - DNA extracted from K₂EDTA anti-coagulated blood stored at 2°C to 4°C for 30 days (claimed in package insert) - DNA extracted from K₂EDTA anti-coagulated blood stored at -15°C to -25°C for 30 days (claimed in package insert) - Genomic DNA subjected to 6 freeze/thaw cycles Additionally, 6 blood samples were divided into 6 aliquots and stored under the following conditions: - 2°C to 8°C for 1 day - -15°C to -25°C for 1 day - 2°C to 8°C for 30 days - -15°C to -25°C for 30 days - Room temperature for 7 days - 30°C for 7 days Extracted blood was then stored at -15°C to -25°C until the study commenced. Fifteen samples aliquoted into 6 tubes were used to assess sample storage claims and 2 aliquots of each sample were used to assess freeze/thaw claims (one sample stored and the other undergoing freeze/thaw once a day for 6 days). Samples included SNVs and DIVs as well as homozygotes, heterozygotes, and compound heterozygotes. Acceptance criteria were based on call rate, sample first-pass rate and reproducibility, and all studies met their acceptance criteria. {24} 25 # Reagent Integrity and Shipping: Shipping studies were designed to evaluate product performance after exposure to simulated shipping conditions. Study elements included atmospheric thermal cycling with both summer and winter profiles depending on the reagent being tested. Reagents believed to be sensitive to heat were subjected to summer profiles (enzymes, oligos, etc), while reagents believed to be sensitive to freeze/thaw were subjected to winter profiles. Distribution testing was also performed to include the following: - Atmospheric pre-conditioning - Shock-drop (8 and 9 drops) - Vibration – Random dynamic load - Random Vibration – Pick-up and Delivery Vehicle Spectrum - Vibration – Random under low pressure vacuum Shipping validation testing was conducted with 8 samples that included deletion/insertion variants (including in a homopolymeric region), SNVs, and 1 large deletion. After shipping testing was complete, all kit components were stored at recommended conditions until functional testing could be performed. Acceptance criteria included the assay requirements (call rate and accuracy ≥ 99%), payload and shipping testing had internal temperature acceptance criteria, and container integrity testing only required no major visual defects (minor defects including punctures, tears, and cracks in the container were acceptable). All testing passed by meeting all acceptance criteria. ## d. Detection Limit (Analytical sensitivity): ### Analytical Sensitivity at High DNA Input: The recommended DNA input for this assay is 250 ng. An initial study was conducted to estimate the performance of the assay when the gDNA input is greater or less than the recommended DNA input concentration. Four different DNA samples were tested at input levels of 1250, 250, 100, and 25 ng. The 4 DNA samples covered 7 mutations and included heterozygous single nucleotide variants (SNVs), heterozygous and homozygous deletion/insertion variants (DIVs), one large deletion, and a deletion cum insertion. Either 20 (1250 ng) or 24 (all other concentrations) replicates were tested for each sample. Samples were processed by 2 operators over 4 days using a single lot of reagents and a single thermal cycler. The same lot of gDNA samples was used throughout the study. Genotype calls were compared to bidirectional Sanger sequencing except for the 2 large deletions which were confirmed using validated duplex PCR followed by sequencing of resulting amplicons. Both assays met the pre-determined acceptance criteria for all concentrations tested. One sample at 25 ng had a call rate of 98% which was deemed unacceptable. There was a single no-call at 1250 ng (both no-calls at 1250 ng were at the PolyTG/PolyT {25} region). At 25 ng there were 140 no-calls with 136 arising from 6 replicates of the same sample. ## Analytical Sensitivity at Low DNA Input: Fourteen DNA specimens were tested at 9 different DNA input levels; 1250, 500, 250, 100, 50, 25, 10, 5, and 1 ng. Variation types tested included SNVs, small insertion/deletions (including F508del), one large deletion, and compound insertion/deletions. A single lot of reagents were used and the same lot of DNA samples and a single thermal cycler were used. This study passed acceptance criteria at all concentrations except 1, 5, and 10 ng (25-fold below recommended DNA input). Based on the results of both studies, the upper and lower bounds for DNA input into the assay are 1250 and 25 ng, respectively. ## e. Analytical Specificity (Interfering Substances): **Bilirubin, Hemoglobin, Cholesterol, and Buffer Component Interference:** The effect of potential interferents on the performance of the assay was examined using 8 samples carrying 8 unique genotypes, and blood from the same individual was tested across all 4 interfering substances. Sample types included 1 PolyTG/PolyT variant, 1 indel (F508del), and 6 SNVs. Bilirubin (684 and 137 μmol/L), hemoglobin (2 and 0.4 g/L), and cholesterol (13 and 2.6 mmol/L) were spiked into blood aliquots prior to DNA extraction. Wash buffer from DNA extraction (15%) was spiked into genomic DNA samples prior to library preparation. For the assessment of each inhibiting substance, data for each spiked sample was compared to an untreated aliquot of the same blood/DNA sample. Impact on call rate, reproducibility, and sample first pass rate were determined. All 88 samples met the acceptance criteria of the test. **Lipid and Short Draw Interference:** A study to assess the potential interference of triglycerides (37 mmol/L and 7.4 mmol/L) and high and low concentrations of K₂EDTA (7 mg/mL and 2.8 mg/mL) to mimic short blood draws was conducted. Eight whole blood samples were used for this study. Two samples were WT, 2 were F508del, and the remaining 4 were SNVs. With the exception of R75Q, all SNVs were replicates of those tested in Interference Study A (above), but were different blood samples. All tested conditions gave 100% correct calls, and no samples required a re-concentration to obtain the appropriate amount of DNA for the assay. ## f. Assay cut-off: Not applicable 26 {26} # g. Sample carryover: The goal of this study was to ascertain that sample carryover between samples within an instrument run and between successive sequencing runs met design requirements. Two genomic DNA samples with unique CFTR genotypes were assessed. One sample had 2 variants and one sample had 3 variants. In the intra-run test, 1 library composed of 2 samples with unique variants was set up in a checkerboard matrix pattern at alternating high (500 ng) and low (100 ng) concentrations along with 4 NTCs. For the inter-run test, 2 libraries were prepared; the library contained either a single distinct genomic DNA sample or one NTC. For both the inter and intra-run tests, sample carryover was assessed by measuring the error rate at the position of variant calls for all samples used in the study. The design input requirement was carryover $\leq 2\%$ . The highest carryover rate seen in this test was $0.31\%$ for intra-run testing and $0.3\%$ for inter-run testing. # 2. Comparison studies: # a. Method comparison to reference method: # Accuracy: Accuracy of the Illumina MiSeqDx Clinical Sequencing Assay was assessed by evaluating 500 samples representing a wide variety of CFTR variants from four separate sources; 369 were clinical gDNA specimens, 79 were cell line gDNA, and 52 were synthetic samples derived from plasmid DNA. Accuracy was based on comparison with Sanger sequencing of all 500 samples over all 5,206 positions interrogated by the MiSeqDx assay. A total of 203 variants from reference were detected. These variants covered most of the 27 exons (with the exception of exons 16 and 26) and an intronic region within CFTR including the PolyTG/PolyT homopolymeric region. Variant types analyzed in the accuracy study included SNVs, small indels, and 2 large deletions. All 23 mutations recommended by the ACMG were included in the study, and all were examined with clinical samples in addition to other sample types. As noted below there were 6 miscalls and 4 no calls in the study. One of the no calls was in the context of wild-type sequence, while the rest were in the context of variants, most notably in the PolyTG/PolyT region. Overall this study met its acceptance criteria. Table 4: Accuracy by Variant | Genotype (Common Name/cDNA name/coordinate) | Variant Type | CFTR gene region (hg19) | Positive calls (Variants) | | | No Calls | Miscalls | PPA (%) | | --- | --- | --- | --- | --- | --- | --- | --- | --- | | | | | Clinical Samples | Cell Line Samples | Synthetic Samples | | | | | 117120141 | SNV | Exon1 | 25 | 3 | 0 | 0 | 0 | 100 | | 117120145 | SNV | Exon1 | 3 | 2 | 0 | 0 | 0 | 100 | | M1V | SNV | Exon1 | 0 | 0 | 1 | 0 | 0 | 100 | {27} | CFTR dele2, 3 | Del | Intron1 | 4 | 1 | 0 | 0 | 0 | 100 | | --- | --- | --- | --- | --- | --- | --- | --- | --- | | R31C | SNV | Exon2 | 3 | 1 | 0 | 0 | 0 | 100 | | Q39X | SNV | Exon2 | 0 | 0 | 1 | 0 | 0 | 100 | | E60X | SNV | Exon3 | 6 | 1 | 0 | 0 | 0 | 100 | | P67L | SNV | Exon3 | 1 | 0 | 1 | 0 | 0 | 100 | | R74W | SNV | Exon3 | 0 | 2 | 0 | 0 | 0 | 100 | | R74Q | SNV | Exon3 | 2 | 0 | 0 | 0 | 0 | 100 | | R75X | SNV | Exon3 | 3 | 1 | 0 | 0 | 0 | 100 | | R75Q | SNV | Exon3 | 20 | 1 | 0 | 0 | 0 | 100 | | G85E | SNV | Exon3 | 6 | 2 | 0 | 0 | 0 | 100 | | 394delTT | DIV | Exon3 | 3 | 1 | 0 | 0 | 0 | 100 | | 405+1G>A | SNV | Intron3 | 0 | 0 | 1 | 0 | 0 | 100 | | 406-1G>A | SNV | Exon4 | 4 | 0 | 0 | 0 | 0 | 100 | | E92K | SNV | Exon4 | 0 | 0 | 1 | 0 | 0 | 100 | | E92X | SNV | Exon4 | 0 | 1 | 1 | 0 | 0 | 100 | | Q98X | SNV | Exon4 | 0 | 0 | 2 | 0 | 0 | 100 | | I105SfsX2 | DIV | Exon4 | 0 | 2 | 0 | 0 | 0 | 100 | | 457TAT>G | DIV | Exon4 | 0 | 0 | 1 | 0 | 0 | 100 | | D110H | SNV | Exon4 | 1 | 0 | 1 | 0 | 0 | 100 | | R117C | SNV | Exon4 | 4 | 0 | 0 | 0 | 0 | 100 | | R117H | SNV | Exon4 | 17 | 2 | 0 | 0 | 0 | 100 | | Y122X | SNV | Exon4 | 0 | 1 | 0 | 0 | 0 | 100 | | F143LfsX10 | DIV | Exon4 | 0 | 1 | 0 | 0 | 0 | 100 | | 574delA | DIV | Exon4 | 0 | 0 | 2 | 0 | 0 | 100 | | Q151K | SNV | Exon4 | 1 | 0 | 0 | 0 | 0 | 100 | | 621+1G>T | SNV | Intron4 | 7 | 5 | 0 | 0 | 0 | 100 | | 621+3A>G | SNV | Intron4 | 1 | 0 | 0 | 0 | 0 | 100 | | 663delT | DIV | Exon5 | 1 | 0 | 1 | 0 | 0 | 100 | | G178R | SNV | Exon5 | 1 | 1 | 0 | 0 | 0 | 100 | | 711+1G>T | SNV | Intron5 | 3 | 1 | 0 | 0 | 0 | 100 | | 711+3A>G | SNV | Intron5 | 0 | 0 | 1 | 0 | 0 | 100 | | 711+5 G->A | SNV | Intron5 | 0 | 0 | 1 | 0 | 0 | 100 | | 712-1 G->T | SNV | Exon6 | 0 | 0 | 1 | 0 | 0 | 100 | | H199Y | SNV | Exon6 | 0 | 0 | 1 | 0 | 0 | 100 | | P205S | SNV | Exon6 | 1 | 0 | 1 | 0 | 0* | 100 | | L206W | SNV | Exon6 | 8 | 1 | 0 | 0 | 0 | 100 | | A209S | SNV | Exon6 | 0 | 1 | 0 | 0 | 0 | 100 | | Q220X | SNV | Exon6 | 0 | 0 | 1 | 0 | 0 | 100 | | L227R | SNV | Exon6 | 0 | 0 | 1 | 0 | 0 | 100 | | 852del22 | DIV | Exon6 | 0 | 0 | 1 | 0 | 0 | 100 | | E279D | SNV | Exon7 | 1 | 0 | 0 | 0 | 0 | 100 | {28} | R297Q | SNV | Exon8 | 2 | 0 | 0 | 0 | 0 | 100 | | --- | --- | --- | --- | --- | --- | --- | --- | --- | | 1078delT | DIV | Exon8 | 1 | 1 | 0 | 0 | 0 | 100 | | L320V | SNV | Exon8 | 1 | 0 | 0 | 0 | 0 | 100 | | G330X | SNV | Exon8 | 1 | 1 | 0 | 0 | 0 | 100 | | R334W | SNV | Exon8 | 6 | 1 | 0 | 0 | 0 | 100 | | I336K | SNV | Exon8 | 0 | 1 | 0 | 0 | 0 | 100 | | T338I | SNV | Exon8 | 0 | 0 | 1 | 0 | 0 | 100 | | 1154insTC | DIV | Exon8 | 0 | 1 | 0 | 0 | 0 | 100 | | S341P | SNV | Exon8 | 0 | 0 | 1 | 0 | 0 | 100 | | R347H | SNV | Exon8 | 6 | 1 | 1 | 0 | 0 | 100 | | R347P | SNV | Exon8 | 3 | 2 | 0 | 0 | 0 | 100 | | R352Q | SNV | Exon8 | 5 | 0 | 0 | 0 | 0 | 100 | | Q359K/T360K | SNV | Exon8 | 0 | 0 | 1 | 0 | 0 | 100 | | 1213delT | DIV | Exon8 | 0 | 0 | 1 | 0 | 0 | 100 | | 1248+1G>A | SNV | Intron8 | 0 | 0 | 1 | 0 | 0 | 100 | | 1259insA | DIV | Exon9 | 0 | 0 | 2 | 0 | 0 | 100 | | W401X(c.1202G>A) | SNV | Exon9 | 0 | 0 | 1 | 0 | 0 | 100 | | W401X(c.1203G>A) | SNV | Exon9 | 0 | 0 | 1 | 0 | 0 | 100 | | 1341+1G->A | SNV | Intron9 | 0 | 0 | 2 | 0 | 0 | 100 | | PolyTGPolyT | PolyTG/PolyT | Intron9 | 369 | 79 | 52 | 3 | 4# | 98.60 | | 1461ins4 | DIV | Exon10 | 0 | 0 | 1 | 0 | 0 | 100 | | A455E | SNV | Exon10 | 4 | 2 | 0 | 0 | 0 | 100 | | 1525-1G->A | SNV | Exon11 | 0 | 0 | 1 | 0 | 0 | 100 | | S466X (C->A) | SNV | Exon11 | 0 | 0 | 1 | 0 | 0 | 100 | | S466X (C->G) | SNV | Exon11 | 1 | 0 | 1 | 0 | 0 | 100 | | L467P | SNV | Exon11 | 0 | 0 | 1 | 0 | 0 | 100 | | V470M | SNV | Exon11 | 311 | 71 | 0 | 0 | 0 | 100 | | 1548delG | DIV | Exon11 | 1 | 0 | 1 | 0 | 0 | 100 | | P477S | SNV | Exon11 | 0 | 1 | 0 | 0 | 0 | 100 | | S485T | SNV | Exon11 | 1 | 0 | 0 | 0 | 0 | 100 | | S489X | SNV | Exon11 | 0 | 0 | 2 | 0 | 0 | 100 | | S492F | SNV | Exon11 | 0 | 0 | 1 | 0 | 0 | 100 | | Q493X | SNV | Exon11 | 4 | 2 | 0 | 0 | 0 | 100 | | I506V | SNV | Exon11 | 7 | 0 | 0 | 0 | 0 | 100 | | I507del | DIV | Exon11 | 4 | 2 | 0 | 0 | 0 | 100 | | F508del | DIV | Exon11 | 84 | 29 | 0 | 0 | 0 | 100 | | I507V | SNV | Exon11 | 0 | 1 | 0 | 0 | 0 | 100 | | F508C | SNV | Exon11 | 1 | 1 | 0 | 0 | 0 | 100 | | 1677delTA | DIV | Exon11 | 1 | 0 | 0 | 0 | 0 | 100 | {29} | V520F | SNV | Exon11 | 2 | 0 | 0 | 0 | 0 | 100 | | --- | --- | --- | --- | --- | --- | --- | --- | --- | | Q525X | SNV | Exon11 | 0 | 0 | 1 | 0 | 0 | 100 | | E527E | SNV | Exon11 | 3 | 2 | 0 | 0 | 0 | 100 | | E528E | SNV | Exon11 | 6 | 2 | 0 | 0 | 0 | 100 | | 1717-8G->A | SNV | Intron11 | 0 | 0 | 1 | 0 | 0 | 100 | | 1717-1G>A | SNV | Exon12 | 4 | 1 | 0 | 0 | 0 | 100 | | G542X | SNV | Exon12 | 12 | 3 | 0 | 0 | 0 | 100 | | S549R(c.1645A>C) | SNV | Exon12 | 0 | 0 | 1 | 0 | 0 | 100 | | S549N | SNV | Exon12 | 2 | 2 | 1 | 0 | 0 | 100 | | S549R(c.1647T>G) | SNV | Exon12 | 3 | 1 | 0 | 0 | 0 | 100 | | G551D | SNV | Exon12 | 8 | 3 | 0 | 0 | 0 | 100 | | Q552X | SNV | Exon12 | 0 | 0 | 1 | 0 | 0 | 100 | | R553X | SNV | Exon12 | 8 | 2 | 0 | 0 | 0 | 100 | | I556V | SNV | Exon12 | 1 | 0 | 0 | 0 | 0 | 100 | | L558S | SNV | Exon12 | 0 | 0 | 1 | 0 | 0 | 100 | | A559T | SNV | Exon12 | 4 | 0 | 1 | 0 | 0 | 100 | | R560K | SNV | Exon12 | 0 | 0 | 1 | 0 | 0 | 100 | | R560T | SNV | Exon12 | 6 | 1 | 0 | 0 | 0 | 100 | | 1811+1.6kb A->G | SNV | Intron12 | 0 | 0 | 1 | 0 | 0 | 100 | | 1812-1 G->A | SNV | Exon13 | 0 | 2 | 0 | 0 | 0 | 100 | | A561T | SNV | Exon13 | 1 | 0 | 0 | 0 | 0 | 100 | | V562I | SNV | Exon13 | 1 | 0 | 0 | 0 | 0 | 100 | | Y569D | SNV | Exon13 | 0 | 0 | 1 | 0 | 0 | 100 | | P574H | SNV | Exon13 | 0 | 1 | 0 | 0 | 0 | 100 | | G576A | SNV | Exon13 | 4 | 1 | 0 | 0 | 0 | 100 | | D579G | SNV | Exon13 | 0 | 0 | 1 | 0 | 0 | 100 | | E585X | SNV | Exon13 | 0 | 0 | 1 | 0 | 0 | 100 | | 1898+1G>A | SNV | Intron13 | 2 | 1 | 0 | 0 | 0 | 100 | | 1898+3A>G | SNV | Intron13 | 0 | 0 | 1 | 0 | 0 | 100 | | H609R | SNV | Exon14 | 0 | 1 | 0 | 0 | 0 | 100 | | D614G | SNV | Exon14 | 0 | 0 | 2 | 0 | 0 | 100 | | R668C | SNV | Exon14 | 5 | 2 | 0 | 0 | 0 | 100 | | R668H | SNV | Exon14 | 1 | 0 | 0 | 0 | 0 | 100 | | 2143delT | DIV | Exon14 | 2 | 1 | 0 | 0 | 0 | 100 | | K684TfsX4 | DIV | Exon14 | 0 | 0 | 1 | 0 | 0 | 100 | | 2183AA>G | DIV | Exon14 | 3 | 1 | 0 | 0 | 0 | 100 | | 2184delA | DIV | Exon14 | 1 | 1 | 0 | 0 | 0 | 100 | | 2184insA | DIV | Exon14 | 3 | 0 | 1 | 0 | 0 | 100 | | S686Y | SNV | Exon14 | 0 | 1 | 0 | 0 | 0 | 100 | | R709X | SNV | Exon14 | 1 | 0 | 2 | 0 | 0 | 100 | {30} | K710X | SNV | Exon14 | 3 | 0 | 0 | 0 | 0 | 100 | | --- | --- | --- | --- | --- | --- | --- | --- | --- | | E725K | SNV | Exon14 | 2 | 0 | 0 | 0 | 0 | 100 | | 2307insA | DIV | Exon14 | 3 | 0 | 2 | 0 | 0 | 100 | | L732X | SNV | Exon14 | 0 | 0 | 2 | 0 | 0 | 100 | | 2347delG | DIV | Exon14 | 0 | 0 | 2 | 0 | 0 | 100 | | P750L | SNV | Exon14 | 1 | 0 | 0 | 0 | 0 | 100 | | V754M | SNV | Exon14 | 2 | 1 | 0 | 0 | 0 | 100 | | R764X | SNV | Exon14 | 1 | 0 | 2 | 0 | 0 | 100 | | 2585delT | DIV | Exon14 | 0 | 0 | 2 | 0 | 0 | 100 | | E822X | SNV | Exon14 | 0 | 0 | 2 | 0 | 0 | 100 | | 2622+1G>A | SNV | Intron14 | 0 | 0 | 2 | 0 | 0 | 100 | | E831X | SNV | Exon15 | 0 | 0 | 1 | 0 | 0 | 100 | | D836Y | SNV | Exon15 | 0 | 1 | 0 | 0 | 0 | 100 | | W846X | SNV | Exon15 | 0 | 1 | 0 | 0 | 0 | 100 | | R851X | SNV | Exon15 | 0 | 0 | 1 | 0 | 0 | 100 | | T854T | SNV | Exon15 | 212 | 44 | 0 | 0 | 0 | 100 | | 2711delT | DIV | Exon15 | 0 | 0 | 1 | 0 | 0 | 100 | | V868V | SNV | Exon15 | 2 | 0 | 0 | 0 | 0 | 100 | | c.2657+2_2657+3 insA | DIV | Intron16 | 0 | 0 | 1 | 0 | 0 | 100 | | 2789+5G>A | SNV | Intron16 | 9 | 1 | 0 | 0 | 0 | 100 | | Q890X | SNV | Exon17 | 1 | 0 | 0 | 0 | 0 | 100 | | A923A | SNV | Exon17 | 1 | 0 | 0 | 0 | 0 | 100 | | L927P | SNV | Exon17 | 0 | 0 | 1 | 0 | 0 | 100 | | S945L | SNV | Exon17 | 0 | 0 | 1 | 0 | 0 | 100 | | M952T | SNV | Exon17 | 1 | 0 | 0 | 0 | 0 | 100 | | 3007delG | DIV | Exon17 | 0 | 0 | 1 | 0 | 0 | 100 | | T966T | SNV | Exon17 | 5 | 0 | 0 | 0 | 0 | 100 | | G970R | SNV | Exon17 | 0 | 0 | 1 | 0 | 0 | 100 | | S977F | SNV | Exon18 | 0 | 0 | 1 | 0 | 0 | 100 | | 3120G>A | SNV | Exon18 | 1 | 0 | 0 | 0 | 0 | 100 | | 3120+1G>A | SNV | Intron18 | 7 | 1 | 0 | 0 | 0 | 100 | | 3121-1G->A | SNV | CF Syn_Ex19 | 0 | 0 | 1 | 0 | 0 | 100 | | L997F | SNV | Exon19 | 2 | 1 | 0 | 0 | 0 | 100 | | I1027T | SNV | Exon19 | 1 | 2 | 0 | 0 | 0 | 100 | | 3272-26A>G | SNV | Intron19 | 0 | 1 | 0 | 0 | 0 | 100 | | F1052V | SNV | Exon20 | 0 | 1 | 0 | 0 | 0 | 100 | | L1065P | SNV | Exon20 | 0 | 0 | 1 | 0 | 0 | 100 | | R1066C | SNV | Exon20 | 6 | 0 | 0 | 0 | 0 | 100 | | R1066H | SNV | Exon20 | 1 | 0 | 1 | 0 | 0 | 100 | | G1069R | SNV | Exon20 | 0 | 1 | 0 | 0 | 0 | 100 | {31} | R1070W | SNV | Exon20 | 0 | 2 | 0 | 0 | 0 | 100 | | --- | --- | --- | --- | --- | --- | --- | --- | --- | | R1070Q | SNV | Exon20 | 0 | 1 | 0 | 0 | 0 | 100 | | L1077P | SNV | Exon20 | 0 | 0 | 1 | 0 | 0^ | 100 | | W1089X | SNV | Exon20 | 4 | 0 | 0 | 0 | 0 | 100 | | Y1092X (C>A) | SNV | Exon20 | 3 | 1 | 0 | 0 | 0 | 100 | | Y1092X (C>G) | SNV | Exon20 | 0 | 0 | 1 | 0 | 0 | 100 | | T1095T | SNV | Exon20 | 7 | 0 | 0 | 0 | 0 | 100 | | M1101K | SNV | Exon20 | 2 | 2 | 0 | 0 | 0 | 100 | | E1104X | SNV | Exon20 | 0 | 0 | 1 | 0 | 0 | 100 | | c.3368-2A>T | SNV | Intron20 | 0 | 1 | 0 | 0 | 0 | 100 | | D1152H | SNV | Exon21 | 10 | 1 | 0 | 0 | 0 | 100 | | V1153E | SNV | Exon21 | 1 | 0 | 0 | 0 | 0 | 100 | | R1158X | SNV | Exon22 | 7 | 1 | 0 | 0 | 0 | 100 | | R1162X | SNV | Exon22 | 5 | 1 | 0 | 0 | 0 | 100 | | R1162L | SNV | Exon22 | 0 | 2 | 0 | 0 | 0 | 100 | | 3659delC | DIV | Exon22 | 4 | 1 | 0 | 0 | 0 | 100 | | S1196X | SNV | Exon22 | 1 | 0 | 0 | 0 | 0 | 100 | | W1204X(c.3611G>A) | SNV | Exon22 | 0 | 0 | 1 | 0 | 0 | 100 | | W1204X(c.3612G>A) | SNV | Exon22 | 0 | 0 | 1 | 0 | 0 | 100 | | 3791delC | DIV | Exon22 | 2 | 0 | 0 | 0 | 0 | 100 | | I1234V | SNV | Exon22 | 1 | 0 | 1 | 0 | 0 | 100 | | S1235R | SNV | Exon22 | 9 | 1 | 0 | 0 | 0 | 100 | | 3849+10kbC>T | SNV | Intron22 | 11 | 2 | 0 | 0 | 0 | 100 | | G1244E | SNV | Exon23 | 0 | 0 | 1 | 0 | 0 | 100 | | 3876delA | DIV | Exon23 | 6 | 1 | 0 | 0 | 0 | 100 | | S1251N | SNV | Exon23 | 1 | 0 | 1 | 0 | 0 | 100 | | 3905insT | DIV | Exon23 | 3 | 1 | 0 | 0 | 0 | 100 | | D1270N | SNV | Exon23 | 0 | 2 | 0 | 0 | 0 | 100 | | W1282X | SNV | Exon23 | 9 | 1 | 0 | 0 | 0 | 100 | | P1290P | SNV | Exon23 | 10 | 3 | 0 | 0 | 0 | 100 | | 4005+1G->A | SNV | Intron23 | 0 | 0 | 1 | 0 | 0 | 100 | | 4016insT | DIV | Exon24 | 0 | 0 | 1 | 0 | 0 | 100 | | T1299T | SNV | Exon24 | 3 | 0 | 0 | 0 | 0 | 100 | | N1303K | SNV | Exon24 | 9 | 1 | 0 | 0 | 0 | 100 | | Q1313X | SNV | Exon24 | 0 | 0 | 1 | 0 | 0 | 100 | | G1349D | SNV | Exon25 | 0 | 1 | 0 | 0 | 0 | 100 | | 4209TGTT>AA | DIV | Exon25 | 0 | 0 | 1 | 0 | 0 | 100 | | CFTRdele22,23 | Del | Intron24 | 1 | 0 | 1 | 0 | 0 | 100 | | 4382delA | DIV | Exon27 | 0 | 0 | 1 | 0 | 0 | 100 | | Y1424Y | SNV | Exon27 | 6 | 2 | 0 | 0 | 0 | 100 | {32} Table 5: Accuracy for the PolyTG/PolyT Tract Variants | Genotype | Clinical Samples | Cell Line Samples | Synthetic Samples | # Miscalls | # No Calls | % Accuracy | | --- | --- | --- | --- | --- | --- | --- | | (TG)9(T)7/(TG)11(T)7 | 2 | 0 | 0 | 0 | 1 | 50.0 | | (TG)9(T)9/(TG)10(T)7 | 1 | 0 | 0 | 0 | 0 | 100 | | (TG)9(T)9/(TG)11(T)7 | 5 | 1 | 0 | 0 | 0 | 100 | | (TG)9(T)9/(TG)11(T)9 | 1 | 0 | 0 | 0 | 0 | 100 | | (TG)10(T)7/(TG)10(T)7 | 25 | 8 | 0 | 0 | 0 | 100 | | (TG)10(T)7/(TG)10(T)9 | 39 | 16 | 0 | 0 | 0 | 100 | | (TG)10(T)7/(TG)11(T)5 | 2 | 0 | 0 |…