ClinVar Miner

Submissions for variant NM_016169.4(SUFU):c.933C>A (p.Thr311=)

gnomAD frequency: 0.00001  dbSNP: rs767071744
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV001019186 SCV001180514 likely benign Hereditary cancer-predisposing syndrome 2017-11-27 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 RCV001452534 SCV001656202 likely benign Gorlin syndrome; Medulloblastoma 2022-11-23 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV004553558 SCV004712163 likely benign SUFU-related disorder 2023-05-19 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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