ClinVar Miner

Submissions for variant NM_000222.3(KIT):c.1635C>T (p.Tyr545=)

dbSNP: rs374123328
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001490058 SCV001694615 likely benign Gastrointestinal stromal tumor 2023-11-08 criteria provided, single submitter clinical testing
Ambry Genetics RCV002399996 SCV002707632 likely benign Hereditary cancer-predisposing syndrome 2022-03-14 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.

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