ClinVar Miner

Submissions for variant NM_000070.3(CAPN3):c.412C>G (p.Leu138Val)

dbSNP: rs1042151947
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001235800 SCV001408505 uncertain significance Autosomal recessive limb-girdle muscular dystrophy type 2A 2021-04-12 criteria provided, single submitter clinical testing This variant has not been reported in the literature in individuals with CAPN3-related conditions. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Probably Damaging"; Align-GVGD: "Class C0"). This variant is not present in population databases (ExAC no frequency). This sequence change replaces leucine with valine at codon 138 of the CAPN3 protein (p.Leu138Val). The leucine residue is highly conserved and there is a small physicochemical difference between leucine and valine.

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