ClinVar Miner

Submissions for variant NM_000546.6(TP53):c.450_459del (p.Pro151fs)

dbSNP: rs137852791
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory of Translational Genomics, National Cancer Institute RCV000119796 SCV000154268 not provided Sarcoma no assertion provided not provided
Seelig Lab, University of Washington RCV000767320 SCV000897886 not provided not provided no assertion provided in vitro

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