ClinVar Miner

Submissions for variant NM_002528.7(NTHL1):c.594C>G (p.Ala198=)

gnomAD frequency: 0.00001  dbSNP: rs1372740198
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV001024983 SCV001187087 likely benign Hereditary cancer-predisposing syndrome 2019-04-24 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
Labcorp Genetics (formerly Invitae), Labcorp RCV001483652 SCV001688048 likely benign not provided 2023-10-04 criteria provided, single submitter clinical testing

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