ClinVar Miner

Submissions for variant NM_005157.6(ABL1):c.756G>T (p.Gln252His)

dbSNP: rs121913458
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000422852 SCV000505080 likely pathogenic Chronic myelogenous leukemia, BCR-ABL1 positive 2015-07-14 no assertion criteria provided literature only

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