ClinVar Miner

Submissions for variant NM_003921.5(BCL10):c.136dup (p.Ile46fs)

dbSNP: rs387906351
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000006637 SCV000026820 pathogenic T-cell acute lymphoblastic leukemia 1999-01-08 no assertion criteria provided literature only
OMIM RCV000023308 SCV000044599 pathogenic Carcinoma of colon 1999-01-08 no assertion criteria provided literature only

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