"Ambry Genetics"[submitter] AND "IFNAR2"[gene] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1444810	NM_001289125.3(IFNAR2):c.27C>G (p.Ile9Met)	IFNAR2, IFNAR2-IL10RB (I9M)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1437130	NM_001289125.3(IFNAR2):c.65G>T (p.Ser22Ile)	IFNAR2, IFNAR2-IL10RB (S22I)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1394635	NM_001289125.3(IFNAR2):c.70G>A (p.Val24Met)	IFNAR2, IFNAR2-IL10RB (V24M)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1438104	NM_001289125.3(IFNAR2):c.127A>T (p.Ile43Leu)	IFNAR2, IFNAR2-IL10RB (I43L)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1897898	NM_001289125.3(IFNAR2):c.268A>G (p.Arg90Gly)	IFNAR2, IFNAR2-IL10RB (R90G)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1366629	NM_001289125.3(IFNAR2):c.326T>C (p.Val109Ala)	IFNAR2, IFNAR2-IL10RB (V109A)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1989324	NM_001289125.3(IFNAR2):c.406C>T (p.Pro136Ser)	IFNAR2, IFNAR2-IL10RB (P136S)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1436863	NM_001289125.3(IFNAR2):c.437A>G (p.Asn146Ser)	IFNAR2, IFNAR2-IL10RB (N146S)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2212332	NM_001289125.3(IFNAR2):c.442A>G (p.Ile148Val)	IFNAR2, IFNAR2-IL10RB (I148V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2482620	NM_001289125.3(IFNAR2):c.581C>T (p.Thr194Ile)	IFNAR2, IFNAR2-IL10RB (T194I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2539731	NM_001289125.3(IFNAR2):c.584A>G (p.Tyr195Cys)	IFNAR2, IFNAR2-IL10RB (Y195C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1523927	NM_001289125.3(IFNAR2):c.593A>G (p.Asp198Gly)	IFNAR2, IFNAR2-IL10RB (D198G)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2225345	NM_001289125.3(IFNAR2):c.760G>A (p.Ala254Thr)	IFNAR2-IL10RB, IFNAR2 (A254T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2360086	NM_001289125.3(IFNAR2):c.823A>T (p.Ser275Cys)	IFNAR2, IFNAR2-IL10RB (S275C)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1431439	NM_001289125.3(IFNAR2):c.1107C>A (p.Asp369Glu)	IFNAR2, IFNAR2-IL10RB (D369E)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1912569	NM_001289125.3(IFNAR2):c.1189A>G (p.Arg397Gly)	IFNAR2, IFNAR2-IL10RB (R397G)	Single nucleotide variant (3 prime UTR variant +1 more)	not provided +1 more	GUncertain significance
Select item 2352179	NM_001289125.3(IFNAR2):c.1222G>A (p.Glu408Lys)	IFNAR2, IFNAR2-IL10RB (E408K)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2309542	NM_001289125.3(IFNAR2):c.1281A>T (p.Leu427Phe)	IFNAR2, IFNAR2-IL10RB (L427F)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1925103	NM_001289125.3(IFNAR2):c.1450C>T (p.Pro484Ser)	IFNAR2, IFNAR2-IL10RB (P484S)	Single nucleotide variant (3 prime UTR variant +2 more)	not provided +1 more	GUncertain significance
Select item 1351758	NM_001289125.3(IFNAR2):c.1468T>C (p.Trp490Arg)	IFNAR2, IFNAR2-IL10RB (W490R)	Single nucleotide variant (3 prime UTR variant +2 more)	Inborn genetic diseases +1 more	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 20