ClinVar Miner

Submissions for variant NM_012433.4(SF3B1):c.1873C>T (p.Arg625Cys)

dbSNP: rs775623976
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000420143 SCV000507364 likely pathogenic Transitional cell carcinoma of the bladder 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000431257 SCV000507365 likely pathogenic B-cell chronic lymphocytic leukemia 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000440401 SCV000507366 likely pathogenic Adenoid cystic carcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000422746 SCV000507367 likely pathogenic Malignant melanoma of skin 2016-05-31 no assertion criteria provided literature only

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