ClinVar Miner

Submissions for variant NM_000526.5(KRT14):c.1109T>C (p.Leu370Pro)

dbSNP: rs1555571799
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000520694 SCV000619039 likely pathogenic not provided 2017-07-18 criteria provided, single submitter clinical testing The L370P variant in the KRT14 gene has not been reported previously as a pathogenic variant, nor as a benign variant, to our knowledge. This variant is not observed in large population cohorts (Lek et al., 2016; 1000 Genomes Consortium et al., 2015; Exome Variant Server). The L370P variant is a semi-conservative amino acid substitution, which occurs at a position within the 2B coil domain (per KIF database), that is conserved across species and is intolerant of change. In addition, in silico analysis predicts this variant is probably damaging to the protein structure/function. According to ACMG criteria, we therefore interpret L370P as a likely pathogenic variant.

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