ClinVar Miner

Submissions for variant NM_172364.5(CACNA2D4):c.419C>G (p.Ala140Gly)

dbSNP: rs202054008
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV001112951 SCV001270666 benign Retinal cone dystrophy 4 2017-04-27 criteria provided, single submitter clinical testing This variant was observed as part of a predisposition screen in an ostensibly healthy population. A literature search was performed for the gene, cDNA change, and amino acid change (where applicable). Publications were found based on this search. The evidence from the literature, in combination with allele frequency data from public databases where available, was sufficient to rule this variant out of causing disease. Therefore, this variant is classified as benign.
Labcorp Genetics (formerly Invitae), Labcorp RCV001517012 SCV001725397 benign not provided 2024-11-27 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003918696 SCV004732159 benign CACNA2D4-related disorder 2019-06-18 no assertion criteria provided clinical testing This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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