ClinVar Miner

Submissions for variant NM_000492.3(CFTR):c.220C>T (p.Arg74Trp) (rs115545701)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 11
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV000224532 SCV000602984 pathogenic not provided 2017-12-29 criteria provided, single submitter clinical testing
Center for Pediatric Genomic Medicine,Children's Mercy Hospital and Clinics RCV000224532 SCV000281538 likely pathogenic not provided 2015-03-23 criteria provided, single submitter clinical testing
Counsyl RCV000177071 SCV000800736 uncertain significance Cystic fibrosis 2017-11-25 criteria provided, single submitter clinical testing
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000224532 SCV000228891 likely pathogenic not provided 2018-08-03 criteria provided, single submitter clinical testing
GeneDx RCV000479747 SCV000568547 uncertain significance not specified 2016-06-10 criteria provided, single submitter clinical testing The R74W variant in the CFTR gene has been reported previously as heterozygous in one individual with CF; no other variants in the CFTR gene were identified in this individual (Claustres et al., 1993). Expression studies in FRT cells showed that D1270N transfected cells displayed decreased chloride transport activity compared to wild type cells (Van Goor et al., 2014). However, an earlier functional study in HeLa cells showed that D1270N transfected cells displayed chloride transport kinetics similar to wild type cells (Fanen et al., 1999). The R74W variant is a non-conservative amino acid substitution, which is likely to impact secondary protein structure as these residues differ in polarity, charge, size and/or other properties. This substitution occurs at a position where amino acids with similar properties to Arginine are tolerated across species. In silico analysis is inconsistent in its predictions as to whether or not the variant is damaging to the protein structure/function. We interpret R74W as a variant of uncertain significance.
Illumina Clinical Services Laboratory,Illumina RCV000177071 SCV000916174 uncertain significance Cystic fibrosis 2016-07-27 criteria provided, single submitter clinical testing The CFTR c.220C>T (p.Arg74Trp) variant is reported in four studies with clinical information. Claustres et al. (1993) report the variant in a compound heterozygous state in an individual with cystic fibrosis (CF). In this case, the p.Arg74Trp variant is found alone. Luzardo et al. (2002) report one patient with CF carrying the p.Arg74Trp variant as part of the complex allele p.[R74W+D1270N] in a heterozygous state. Claustres et al. (2004) report three patients with congenital absence of the vas deferens (CBAVD) carrying the complex allele p.[R74W+p.D1270N+p.V201M]. They also report two non-CF or asymptomatic patients carrying the p.[R74W+D1270N] complex allele in a heterozygous state and one CF patient with the p.[R74W+D1270N] complex allele in a compound heterozygous state with another missense variant. de Prada Merino et al. (2010) report the p.Arg74Trp variant in an individual with CF in a compound heterozygous state as part of the complex allele p.[R74W+R1070W+D1270N]. Control data are unavailable for this variant, which is reported at a frequency of 0.03540 in the Mandinka in the Gambia population of the 1000 Genomes Project. The evidence for this variant alone is limited. The p.Arg74Trp variant is therefore classified as a variant of unknown significance but suspicious for pathogenicity for CFTR-related disorders. This variant was observed by ICSL as part of a predisposition screen in an ostensibly healthy population.
Integrated Genetics/Laboratory Corporation of America RCV000224532 SCV000696886 uncertain significance not provided 2016-12-27 criteria provided, single submitter clinical testing
Invitae RCV000177071 SCV000562311 benign Cystic fibrosis 2017-11-16 criteria provided, single submitter clinical testing
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000479747 SCV000967179 likely benign not specified 2018-07-06 criteria provided, single submitter clinical testing The p.Arg74Trp variant in CFTR has been reported as a complex allele (p.[Arg74Tr p;Asp1270Asn] or p.[Arg74Trp;Val201Met;Asp1270Asn]) in several individuals with CFTR-related conditions (Aguiano 1992, Casals 1995, Fanen 1999, Padoa 1999, Ravn ik-Glavac 2000, Luzardo 2002, Girodon 2002, Masson 2013, Sosnay 2013, Terlizzi 2 017, Behar 2017, Claustres 20004, Brugnon 2008, de Prada Merino 2010, Steiner 20 11). However, it has also been reported in 1 unaffected child who carried the p. [Arg74Trp;Asp1270Asn] complex allele in trans with a known pathogenic variant (T erlizzi 2017) and in unaffected twins who carried the p.[Arg74Trp;Val201Met;Asp1 270Asn] complex allele in trans with p.Phe508del (Terlizzi 2017, Brugnon 2008). In addition, the p.Arg74Trp variant has been identified in 1.3% (311/24024) of A frican chromosomes, including 3 homozygotes, by the Genome Aggregation Database (gnomAD, http://gnomad.broadinstitute.org). An in vitro functional study suggest ed that the p.Arg74Trp variant did not impact protein function (Fanen 1999). Due to its high frequency in GnomAD and observation in unaffecteds, the p.Arg74Trp variant is classified as likely benign. ACMG/AMP Criteria applied: BS1.
PharmGKB RCV000660770 SCV000783009 drug response ivacaftor response - Efficacy 2018-03-22 reviewed by expert panel curation PharmGKB Level of Evidence 1A: Annotation for a variant-drug combination in a CPIC or medical society-endorsed PGx guideline, or implemented at a PGRN site or in another major health system.
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000224532 SCV000601070 likely pathogenic not provided 2017-07-20 criteria provided, single submitter clinical testing

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.