ClinVar Miner

Submissions for variant NM_000546.6(TP53):c.219G>T (p.Val73=)

dbSNP: rs1567556473
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001175760 SCV001339472 likely benign Hereditary cancer-predisposing syndrome 2019-05-21 criteria provided, single submitter clinical testing
Invitae RCV002068145 SCV002428456 likely benign Li-Fraumeni syndrome 2021-08-09 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001175760 SCV002582274 likely benign Hereditary cancer-predisposing syndrome 2022-06-18 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002290610 SCV002582936 likely benign Li-Fraumeni syndrome 1 2022-06-18 criteria provided, single submitter clinical testing

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