ClinVar Miner

Submissions for variant NM_000546.6(TP53):c.594_611del (p.Gly199_Glu204del)

dbSNP: rs1567551704
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Cancer Genomics Laboratory, Texas Children's Hospital RCV000679849 SCV000804853 likely pathogenic Small cell carcinoma of the ovary, hypercalcemic type 2018-06-01 no assertion criteria provided clinical testing

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