ClinVar Miner

Submissions for variant NM_000546.5(TP53):c.74+38C>G (rs1642785)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000250671 SCV000305120 benign not specified criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV001282982 SCV000605415 benign none provided 2020-07-04 criteria provided, single submitter clinical testing
Color Health, Inc RCV000580249 SCV000686765 benign Hereditary cancer-predisposing syndrome 2015-03-31 criteria provided, single submitter clinical testing
Invitae RCV001520662 SCV001729823 benign Li-Fraumeni syndrome 2020-12-04 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000250671 SCV000692102 likely benign not specified no assertion criteria provided clinical testing

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