Related gene-specific medical variations for Gene (Select 8412) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3260589	NM_003567.4(BCAR3):c.394G>A (p.Glu132Lys)	BCAR3, BCAR3-AS1 (E20K +8 more)	Single nucleotide variant (non-coding transcript variant +3 more)	not specified	GUncertain significance
Select item 2515762	NM_003567.4(BCAR3):c.449G>A (p.Arg150His)	BCAR3, BCAR3-AS1 (R162H +8 more)	Single nucleotide variant (non-coding transcript variant +3 more)	not specified	GUncertain significance
Select item 2476254	NM_003567.4(BCAR3):c.376A>C (p.Ile126Leu)	BCAR3, BCAR3-AS1 (I126L +7 more)	Single nucleotide variant (non-coding transcript variant +3 more)	not specified	GUncertain significance
Select item 2404984	NM_003567.4(BCAR3):c.469G>A (p.Gly157Ser)	BCAR3, BCAR3-AS1 (G169S +8 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2403069	NM_003567.4(BCAR3):c.472C>T (p.Arg158Cys)	BCAR3, BCAR3-AS1 (R183C +8 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 993827	NM_003567.4(BCAR3):c.2273G>A (p.Arg758Gln)	BCAR3 (R434Q +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 993628	NM_003567.4(BCAR3):c.1073G>A (p.Ser358Asn)	BCAR3 (S267N +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

ClinVar