List of variants in gene BCR reported as uncertain significance for Chronic myelogenous leukemia, BCR-ABL1 positive; Acute lymphoid leukemia

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_004327.4(BCR):c.2356G>A (p.Ala786Thr)	rs1259370853	0.00002
NM_004327.4(BCR):c.1149C>T (p.Pro383=)	rs775817981	0.00001
NM_004327.4(BCR):c.685C>T (p.Pro229Ser)	rs1441856766	0.00001

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