Related gene-specific medical variations for Gene (Select 613) - ClinVar - NCBI

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Links from Gene

Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2652962	NM_004327.4(BCR):c.2783-15C>T	BCR, LOC107963955	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2652961	NM_004327.4(BCR):c.2782+511G>A	BCR, LOC107963955	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2652960	NM_004327.4(BCR):c.2708-69A>G	BCR, LOC107963955	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2604169	NM_004327.4(BCR):c.2095A>G (p.Met699Val)	BCR, LOC107963947 (M699V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 756675	NM_004327.4(BCR):c.2808T>C (p.Asp936=)	BCR, LOC107963955	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 721892	NM_004327.4(BCR):c.2708-4G>A	BCR, LOC107963955	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 720880	NM_004327.4(BCR):c.2793C>T (p.Cys931=)	BCR, LOC107963955	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 717145	NM_004327.4(BCR):c.2116-6C>G	BCR, LOC107963947	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 708733	NM_004327.4(BCR):c.2116-7C>A	BCR, LOC107963947	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 691593	t(8;22)(p11;q11)	BCR, FGFR1	Translocation	Myeloid neoplasm associated with FGFR1 rearrangement	GPathogenic
Select item 218629	NM_004327.4(BCR):c.2845G>A (p.Val949Ile)	BCR, LOC107963955 (V949I)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign/Likely benign
Select item 143222	NM_004327.4(BCR):c.2750T>A (p.Val917Asp)	BCR, LOC107963955 (V917D)	Single nucleotide variant (missense variant)	Chronic myelogenous leukemia, BCR-ABL1 positive	Gnot provided
Select item 143221	NM_004327.4(BCR):c.2707+21G>T	BCR	Single nucleotide variant (intron variant)	Chronic myelogenous leukemia, BCR-ABL1 positive	Gnot provided
Select item 143220	NM_004327.4(BCR):c.2699A>G (p.Asn900Ser)	BCR (N900S)	Single nucleotide variant (missense variant)	Chronic myelogenous leukemia, BCR-ABL1 positive	Gnot provided