ClinVar Miner

Submissions for variant NM_000218.3(KCNQ1):c.104C>T (p.Pro35Leu)

dbSNP: rs1373379406
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001042344 SCV001206021 uncertain significance Long QT syndrome 2021-08-27 criteria provided, single submitter clinical testing This sequence change replaces proline with leucine at codon 35 of the KCNQ1 protein (p.Pro35Leu). The proline residue is moderately conserved and there is a moderate physicochemical difference between proline and leucine. The frequency data for this variant in the population databases is considered unreliable, as metrics indicate insufficient coverage at this position in the ExAC database. This variant has not been reported in the literature in individuals affected with KCNQ1-related conditions. 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: "Benign"; Align-GVGD: "Class C0"). 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.

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