Related gene-specific medical variations for Gene (Select 80124) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3188367	NM_025054.5(VCPIP1):c.67A>G (p.Thr23Ala)	LOC130000540, VCPIP1 (T23A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188362	NM_025054.5(VCPIP1):c.262G>A (p.Val88Met)	LOC130000540, VCPIP1 (V88M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188358	NM_025054.5(VCPIP1):c.107T>C (p.Leu36Pro)	LOC130000540, VCPIP1 (L36P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554557	NM_025054.5(VCPIP1):c.46C>T (p.Pro16Ser)	LOC130000540, VCPIP1 (P16S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538937	NM_025054.5(VCPIP1):c.500C>T (p.Ala167Val)	LOC130000540, VCPIP1 (A167V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385706	NM_025054.5(VCPIP1):c.100G>C (p.Gly34Arg)	LOC130000540, VCPIP1 (G34R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273953	NM_025054.5(VCPIP1):c.153T>A (p.Asp51Glu)	LOC130000540, VCPIP1 (D51E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar