ClinVar Miner

Submissions for variant NM_001195626.3(MLLT10):c.1226G>C (p.Gly409Ala)

dbSNP: rs150803413
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV001336718 SCV001530182 uncertain significance Acute myeloid leukemia 2018-03-22 criteria provided, single submitter clinical testing This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].

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