ClinVar Miner

Submissions for variant NM_005343.4(HRAS):c.231C>T (p.Gly77=)

gnomAD frequency: 0.00001  dbSNP: rs1182602668
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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 RCV000911535 SCV001056606 likely benign Costello syndrome 2023-07-06 criteria provided, single submitter clinical testing

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