ClinVar Miner

Submissions for variant NM_005157.6(ABL1):c.1075T>A (p.Phe359Ile)

dbSNP: rs121913452
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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) RCV000424157 SCV000505123 likely pathogenic Chronic myelogenous leukemia, BCR-ABL1 positive 2014-12-26 no assertion criteria provided literature only

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