ANXA2[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2255841	NM_004039.3(ANXA2):c.876G>T (p.Met292Ile)	ANXA2 (M292I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299617	NM_004039.3(ANXA2):c.834G>A (p.Met278Ile)	ANXA2 (M296I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299606	NM_004039.3(ANXA2):c.658C>T (p.Arg220Trp)	ANXA2 (R220W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3127275	NM_004039.3(ANXA2):c.640A>G (p.Ile214Val)	ANXA2 (I214V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299595	NM_004039.3(ANXA2):c.512T>C (p.Met171Thr)	ANXA2 (M189T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3127274	NM_004039.3(ANXA2):c.507G>C (p.Lys169Asn)	ANXA2 (K169N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3127273	NM_004039.3(ANXA2):c.440A>T (p.Tyr147Phe)	ANXA2 (Y147F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3127272	NM_004039.3(ANXA2):c.361C>A (p.Leu121Met)	ANXA2 (L121M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1238049	NM_004039.3(ANXA2):c.292G>T (p.Val98Leu)	ANXA2 (V116L +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3127271	NM_004039.3(ANXA2):c.201G>C (p.Gln67His)	ANXA2 (Q67H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299615	NM_004039.3(ANXA2):c.88T>C (p.Tyr30His)	ANXA2 (Y30H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243243	NM_004039.3(ANXA2):c.10G>A (p.Val4Ile)	ANXA2 (V4I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance