ClinVar Miner

Submissions for variant NM_003640.5(ELP1):c.934G>A (p.Glu312Lys)

gnomAD frequency: 0.02197  dbSNP: rs1140064
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Total submissions: 9
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000125398 SCV000168850 benign not specified 2014-04-03 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Illumina Laboratory Services, Illumina RCV000359268 SCV000476584 likely benign 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 and internal cut-off values, a variant classified as likely benign is not then subjected to further curation. The score for this variant resulted in a classification of likely benign for this disease.
Invitae RCV000857368 SCV000563257 benign not provided 2024-02-01 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV000359268 SCV000743228 benign Familial dysautonomia 2014-10-09 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000857368 SCV001159113 benign not provided 2023-11-29 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV000359268 SCV001737228 benign Familial dysautonomia 2021-05-18 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000125398 SCV003922909 likely benign not specified 2023-03-28 criteria provided, single submitter clinical testing
Natera, Inc. RCV000359268 SCV001452215 benign Familial dysautonomia 2020-04-14 no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV000125398 SCV001924430 benign not specified no assertion criteria provided clinical testing

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