ClinVar Miner

Submissions for variant NM_004327.4(BCR):c.606C>T (p.Ser202=)

gnomAD frequency: 0.00655  dbSNP: rs147507158
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000961729 SCV001108781 benign not provided 2018-08-16 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002503008 SCV002813093 likely benign Chronic myelogenous leukemia, BCR-ABL1 positive; Acute lymphoid leukemia 2022-04-05 criteria provided, single submitter clinical testing

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