ClinVar Miner

Submissions for variant NM_003640.5(ELP1):c.1911T>C (p.Val637=)

gnomAD frequency: 0.00038  dbSNP: rs369645371
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Total submissions: 8
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000278309 SCV000476571 uncertain significance Familial dysautonomia 2018-01-13 criteria provided, single submitter clinical testing This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score, this variant could not be ruled out of causing disease and therefore its association with disease required further investigation. A literature search was performed for the gene, cDNA change, and amino acid change (if applicable). No publications were found based on this search. This variant was therefore classified as a variant of unknown significance for this disease.
Invitae RCV001450077 SCV000626008 likely benign not provided 2024-01-30 criteria provided, single submitter clinical testing
GeneDx RCV001450077 SCV001856587 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Ambry Genetics RCV003298415 SCV003993370 likely benign Inborn genetic diseases 2023-05-19 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
CeGaT Center for Human Genetics Tuebingen RCV001450077 SCV004158541 likely benign not provided 2022-09-01 criteria provided, single submitter clinical testing ELP1: BP4, BP7
Clinical Genetics, Academic Medical Center RCV001450077 SCV001920297 likely benign not provided no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001450077 SCV001928498 likely benign not provided no assertion criteria provided clinical testing
Natera, Inc. RCV000278309 SCV002082106 likely benign Familial dysautonomia 2017-11-14 no assertion criteria provided clinical testing

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