ClinVar Miner

Submissions for variant NM_080911.3(UNG):c.771T>C (p.Tyr257=)

gnomAD frequency: 0.00003  dbSNP: rs1054086515
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002141153 SCV002462171 likely benign Hyper-IgM syndrome type 5 2021-05-31 criteria provided, single submitter clinical testing

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