ClinVar Miner

Submissions for variant NM_012433.4(SF3B1):c.1998G>C (p.Lys666Asn)

dbSNP: rs377023736
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000420231 SCV000504638 likely pathogenic Acute myeloid leukemia 2014-10-02 no assertion criteria provided literature only
Sung Lab, Department of Medicine, Roswell Park Comprehensive Cancer Center RCV000420231 SCV003932626 pathogenic Acute myeloid leukemia 2023-06-08 no assertion criteria provided clinical testing

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