ClinVar Miner

Submissions for variant NM_016169.4(SUFU):c.978A>C (p.Pro326=)

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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 RCV002387186 SCV002695166 likely benign Hereditary cancer-predisposing syndrome 2021-04-06 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 RCV005209584 SCV005850392 likely benign Gorlin syndrome; Medulloblastoma 2025-01-08 criteria provided, single submitter clinical testing

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