Related gene-specific medical variations for Gene (Select 10451) - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3188305	NM_006113.5(VAV3):c.67G>A (p.Val23Met)	VAV3, VAV3-AS1 (V23M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188298	NM_006113.5(VAV3):c.19T>G (p.Cys7Gly)	VAV3, VAV3-AS1 (C7G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188288	NM_006113.5(VAV3):c.106A>G (p.Thr36Ala)	VAV3, VAV3-AS1 (T36A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621448	NM_006113.5(VAV3):c.163A>G (p.Ile55Val)	VAV3, VAV3-AS1 (I55V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536598	NM_006113.5(VAV3):c.117T>A (p.Asp39Glu)	VAV3, VAV3-AS1 (D39E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378980	NM_006113.5(VAV3):c.154G>A (p.Ala52Thr)	VAV3, VAV3-AS1 (A52T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2327157	NM_006113.5(VAV3):c.165C>G (p.Ile55Met)	VAV3, VAV3-AS1 (I55M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212857	NM_006113.5(VAV3):c.71C>T (p.Thr24Ile)	VAV3, VAV3-AS1 (T24I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1808144	GRCh37/hg19 1p13.3(chr1:108064478-108392992)x3	VAV3	Copy number gain	not provided	GUncertain significance
Select item 741943	NM_006113.5(VAV3):c.9G>C (p.Pro3=)	VAV3, VAV3-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 723111	NM_006113.5(VAV3):c.9G>A (p.Pro3=)	VAV3, VAV3-AS1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 709763	NM_006113.5(VAV3):c.73T>C (p.Trp25Arg)	VAV3, VAV3-AS1 (W25R)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 685281	GRCh37/hg19 1p13.3(chr1:108231422-108474521)x1	VAV3	Copy number loss	not provided	GUncertain significance
Select item 221414	GRCh37/hg19 1p13.3(chr1:108115974-108313305)x3	VAV3	Copy number gain	Breast ductal adenocarcinoma	GUncertain significance