IFNA2[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2308280	NM_000605.4(IFNA2):c.544G>C (p.Glu182Gln)	IFNA2 (E182Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343735	NM_000605.4(IFNA2):c.541C>A (p.Gln181Lys)	IFNA2 (Q181K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 781165	NM_000605.4(IFNA2):c.537C>T (p.Asn179=)	IFNA2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 778411	NM_000605.4(IFNA2):c.513G>A (p.Met171Ile)	IFNA2 (M171I)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3108247	NM_000605.4(IFNA2):c.484G>A (p.Ala162Thr)	IFNA2 (A162T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285354	NM_000605.4(IFNA2):c.476G>A (p.Ser159Asn)	IFNA2 (S159N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391423	NM_000605.4(IFNA2):c.451C>T (p.Leu151Phe)	IFNA2 (L151F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286875	NM_000605.4(IFNA2):c.401T>C (p.Met134Thr)	IFNA2 (M134T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491121	NM_000605.4(IFNA2):c.376G>A (p.Val126Met)	IFNA2 (V126M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322395	NM_000605.4(IFNA2):c.376G>T (p.Val126Leu)	IFNA2 (V126L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495023	NM_000605.4(IFNA2):c.361T>G (p.Cys121Gly)	IFNA2 (C121G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285355	NM_000605.4(IFNA2):c.293C>A (p.Ala98Asp)	IFNA2 (A98D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308279	NM_000605.4(IFNA2):c.257T>C (p.Ile86Thr)	IFNA2 (I86T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2308275	NM_000605.4(IFNA2):c.244A>G (p.Met82Val)	IFNA2 (M82V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108246	NM_000605.4(IFNA2):c.243G>C (p.Glu81Asp)	IFNA2 (E81D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484651	NM_000605.4(IFNA2):c.197T>C (p.Phe66Ser)	IFNA2 (F66S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 783545	NM_000605.4(IFNA2):c.170A>G (p.His57Arg)	IFNA2 (H57R)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 786570	NM_000605.4(IFNA2):c.137G>A (p.Arg46Lys)	IFNA2 (R46K)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 778412	NM_000605.4(IFNA2):c.17C>A (p.Ala6Asp)	IFNA2 (A6D)	Single nucleotide variant (missense variant)	not provided	GBenign