ClinVar Miner

Submissions for variant NM_016169.4(SUFU):c.444G>A (p.Val148=)

gnomAD frequency: 0.00001  dbSNP: rs757424197
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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 RCV001447936 SCV001651016 likely benign Gorlin syndrome; Medulloblastoma 2021-07-08 criteria provided, single submitter clinical testing
Ambry Genetics RCV002332916 SCV002634119 likely benign Hereditary cancer-predisposing syndrome 2020-02-04 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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