ClinVar Miner

Submissions for variant NM_201384.3(PLEC):c.13112C>T (p.Ala4371Val)

dbSNP: rs1820690934
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001217958 SCV001389821 uncertain significance Epidermolysis bullosa simplex 5B, with muscular dystrophy; Epidermolysis bullosa simplex, Ogna type; Epidermolysis bullosa simplex 5C, with pyloric atresia; Autosomal recessive limb-girdle muscular dystrophy type 2Q; Epidermolysis bullosa simplex with nail dystrophy 2022-02-05 criteria provided, single submitter clinical testing This variant has not been reported in the literature in individuals affected with PLEC-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces alanine, which is neutral and non-polar, with valine, which is neutral and non-polar, at codon 4398 of the PLEC protein (p.Ala4398Val). ClinVar contains an entry for this variant (Variation ID: 946987). 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 (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be disruptive.
Revvity Omics, Revvity RCV003132283 SCV003809023 uncertain significance not provided 2019-08-22 criteria provided, single submitter clinical testing

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