ClinVar Miner

Submissions for variant NM_002528.7(NTHL1):c.74G>T (p.Arg25Met)

dbSNP: rs2302172
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001224653 SCV001396867 uncertain significance not provided 2019-05-08 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 are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Not Available"; PolyPhen-2: "Benign"; Align-GVGD: "Not Available"). This variant has not been reported in the literature in individuals with NTHL1-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change replaces arginine with methionine at codon 33 of the NTHL1 protein (p.Arg33Met). The arginine residue is weakly conserved and there is a moderate physicochemical difference between arginine and methionine.

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