IFNA10[gene] and "single gene"[properties] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3108228	NM_002171.2(IFNA10):c.565G>A (p.Asp189Asn)	IFNA10 (D189N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383833	NM_002171.2(IFNA10):c.551G>T (p.Arg184Ile)	IFNA10 (R184I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250300	NM_002171.2(IFNA10):c.544C>A (p.Gln182Lys)	IFNA10 (Q182K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108227	NM_002171.2(IFNA10):c.527C>T (p.Ser176Leu)	IFNA10 (S176L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108226	NM_002171.2(IFNA10):c.523C>T (p.Leu175Phe)	IFNA10 (L175F)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2371955	NM_002171.2(IFNA10):c.519A>T (p.Arg173Ser)	IFNA10 (R173S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389615	NM_002171.2(IFNA10):c.437A>C (p.Tyr146Ser)	IFNA10 (Y146S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108225	NM_002171.2(IFNA10):c.410A>T (p.Glu137Val)	IFNA10 (E137V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108224	NM_002171.2(IFNA10):c.403A>T (p.Met135Leu)	IFNA10 (M135L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370255	NM_002171.2(IFNA10):c.398C>A (p.Pro133His)	IFNA10 (P133H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393334	NM_002171.2(IFNA10):c.385G>A (p.Val129Met)	IFNA10 (V129M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108223	NM_002171.2(IFNA10):c.280G>A (p.Glu94Lys)	IFNA10 (E94K)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2428777	NM_002171.2(IFNA10):c.253C>T (p.Gln85Ter)	IFNA10 (Q85*)	Single nucleotide variant (nonsense)	Susceptibility to severe COVID-19	GLikely risk allele
Select item 3108222	NM_002171.2(IFNA10):c.215A>G (p.Gln72Arg)	IFNA10 (Q72R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2267395	NM_002171.2(IFNA10):c.205A>C (p.Asn69His)	IFNA10 (N69H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486847	NM_002171.2(IFNA10):c.199G>A (p.Asp67Asn)	IFNA10 (D67N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285342	NM_002171.2(IFNA10):c.194A>T (p.Glu65Val)	IFNA10 (E65V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406454	NM_002171.2(IFNA10):c.152C>G (p.Ser51Cys)	IFNA10 (S51C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367486	NM_002171.2(IFNA10):c.143C>G (p.Ser48Cys)	IFNA10 (S48C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391231	NM_002171.2(IFNA10):c.141C>G (p.Ile47Met)	IFNA10 (I47M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108220	NM_002171.2(IFNA10):c.133G>C (p.Gly45Arg)	IFNA10 (G45R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2341810	NM_002171.2(IFNA10):c.114G>T (p.Leu38Phe)	IFNA10 (L38F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 768283	NM_002171.2(IFNA10):c.97G>C (p.Gly33Arg)	IFNA10 (G33R)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 768284	NM_002171.2(IFNA10):c.92G>C (p.Ser31Thr)	IFNA10 (S31T)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2257680	NM_002171.2(IFNA10):c.43A>C (p.Ser15Arg)	IFNA10 (S15R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 25