ClinVar Miner

Submissions for variant NM_014000.2(VCL):c.2905G>A (p.Ala969Thr) (rs199751261)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000756900 SCV000884873 uncertain significance not provided 2017-12-26 criteria provided, single submitter clinical testing The VCL p.Ala969Thr variant (rs199751261) has not been reported in the medical literature, is not listed in gene-specific variant databases, has not been previously identified in our laboratory, and is listed in the Genome Aggregation Database (gnomAD) browser with an overall allele frequency of 0.0012% (identified in 3 out of 246,210 chromosomes). The alanine at codon 969 is highly conserved considering 13 species up to C. elegans (Alamut software v2.10.0), but computational analyses predict conflicting effects of this variant on protein structure/function (SIFT: tolerated, PolyPhen2: probably damaging, MutationTaster: disease causing). Based on the available information, the clinical significance of the p.Ala969Thr variant cannot be determined with certainty.

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