ClinVar Miner

Submissions for variant NM_012433.3(SF3B1):c.1996A>G (p.Lys666Glu) (rs754688962)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000421290 SCV000504641 likely pathogenic Neoplasm of the breast 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000431560 SCV000504642 likely pathogenic Chronic lymphocytic leukemia 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000440031 SCV000504643 likely pathogenic Acute myeloid leukemia 2014-10-02 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000422376 SCV000504644 likely pathogenic Hepatocellular carcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000432266 SCV000504645 likely pathogenic Malignant melanoma of skin 2016-05-31 no assertion criteria provided literature only

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