ClinVar Miner

Submissions for variant NM_002957.6(RXRA):c.1280C>T (p.Ser427Phe)

dbSNP: rs1057519958
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000437431 SCV000507337 likely pathogenic Hepatocellular carcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000419754 SCV000507338 likely pathogenic Transitional cell carcinoma of the bladder 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000425675 SCV000507339 likely pathogenic Pancreatic adenocarcinoma 2016-05-31 no assertion criteria provided literature only

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