ClinVar Miner

Submissions for variant NM_000546.6(TP53):c.789T>C (p.Asn263=)

dbSNP: rs770598448
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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 RCV005056402 SCV005705902 likely benign Li-Fraumeni syndrome 2024-12-30 criteria provided, single submitter clinical testing
True Health Diagnostics RCV000664297 SCV000788226 likely benign Hereditary cancer-predisposing syndrome 2017-10-16 no assertion criteria provided clinical testing

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