Related gene-specific medical variations for Gene (Select 389289) - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3299628	NM_001014279.3(ANXA2R):c.329C>T (p.Ala110Val)	ANXA2R, ANXA2R-OT1 (A110V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3127281	NM_001014279.3(ANXA2R):c.496C>G (p.Leu166Val)	ANXA2R, ANXA2R-OT1 (L166V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3127280	NM_001014279.3(ANXA2R):c.433T>G (p.Leu145Val)	ANXA2R, ANXA2R-OT1 (L145V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3127279	NM_001014279.3(ANXA2R):c.418G>A (p.Asp140Asn)	ANXA2R, ANXA2R-OT1 (D140N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3127278	NM_001014279.3(ANXA2R):c.373A>G (p.Ser125Gly)	ANXA2R, ANXA2R-OT1 (S125G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3127277	NM_001014279.3(ANXA2R):c.35C>A (p.Ala12Asp)	ANXA2R, ANXA2R-OT1 (A12D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3127276	NM_001014279.3(ANXA2R):c.176G>A (p.Ser59Asn)	ANXA2R, ANXA2R-OT1 (S59N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597809	NM_001014279.3(ANXA2R):c.34G>A (p.Ala12Thr)	ANXA2R, ANXA2R-OT1 (A12T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543989	NM_001014279.3(ANXA2R):c.391G>A (p.Asp131Asn)	ANXA2R, ANXA2R-OT1 (D131N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539577	NM_001014279.3(ANXA2R):c.451C>T (p.Pro151Ser)	ANXA2R, ANXA2R-OT1 (P151S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470862	NM_001014279.3(ANXA2R):c.67C>G (p.Gln23Glu)	ANXA2R, ANXA2R-OT1 (Q23E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367408	NM_001014279.3(ANXA2R):c.413T>G (p.Val138Gly)	ANXA2R, ANXA2R-OT1 (V138G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360084	NM_001014279.3(ANXA2R):c.497T>C (p.Leu166Pro)	ANXA2R, ANXA2R-OT1 (L166P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295678	NM_001014279.3(ANXA2R):c.344G>C (p.Arg115Thr)	ANXA2R, ANXA2R-OT1 (R115T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272650	NM_001014279.3(ANXA2R):c.449C>T (p.Pro150Leu)	ANXA2R, ANXA2R-OT1 (P150L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance