ClinVar Miner

Submissions for variant NM_001378969.1(KCND3):c.436C>T (p.Arg146Trp)

dbSNP: rs575658111
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001931429 SCV002198563 uncertain significance Spinocerebellar ataxia type 19/22 2021-01-26 criteria provided, single submitter clinical testing 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, but these predictions have not been confirmed by published functional studies and their clinical significance is uncertain. This variant has not been reported in the literature in individuals with KCND3-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change replaces arginine with tryptophan at codon 146 of the KCND3 protein (p.Arg146Trp). The arginine residue is highly conserved and there is a moderate physicochemical difference between arginine and tryptophan.

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