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

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Items: 32

	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)	not provided +1 more	GUncertain significance
Select item 3285366	NM_001289125.3(IFNAR2):c.32G>C (p.Arg11Thr)	IFNAR2, IFNAR2-IL10RB (R11T)	Single nucleotide variant (missense variant)	not specified	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-IL10RB, IFNAR2 (V24M)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1913560	NM_001289125.3(IFNAR2):c.122T>C (p.Phe41Ser)	IFNAR2, IFNAR2-IL10RB (F41S)	Single nucleotide variant (missense variant)	not provided +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 specified +1 more	GUncertain significance
Select item 3108287	NM_001289125.3(IFNAR2):c.197A>G (p.Tyr66Cys)	IFNAR2, IFNAR2-IL10RB (Y66C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1897898	NM_001289125.3(IFNAR2):c.268A>G (p.Arg90Gly)	IFNAR2, IFNAR2-IL10RB (R90G)	Single nucleotide variant (missense variant)	not specified +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 specified +1 more	GUncertain significance
Select item 3285367	NM_001289125.3(IFNAR2):c.353C>T (p.Thr118Met)	IFNAR2, IFNAR2-IL10RB (T118M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1989324	NM_001289125.3(IFNAR2):c.406C>T (p.Pro136Ser)	IFNAR2, IFNAR2-IL10RB (P136S)	Single nucleotide variant (missense variant)	not provided +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)	not specified	GUncertain significance
Select item 1460822	NM_001289125.3(IFNAR2):c.498A>C (p.Leu166Phe)	IFNAR2, IFNAR2-IL10RB (L166F)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2482620	NM_001289125.3(IFNAR2):c.581C>T (p.Thr194Ile)	IFNAR2, IFNAR2-IL10RB (T194I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539731	NM_001289125.3(IFNAR2):c.584A>G (p.Tyr195Cys)	IFNAR2, IFNAR2-IL10RB (Y195C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1523927	NM_001289125.3(IFNAR2):c.593A>G (p.Asp198Gly)	IFNAR2, IFNAR2-IL10RB (D198G)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2225345	NM_001289125.3(IFNAR2):c.760G>A (p.Ala254Thr)	IFNAR2, IFNAR2-IL10RB (A254T)	Single nucleotide variant (missense variant +1 more)	not specified	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)	not specified	GUncertain significance
Select item 1523705	NM_001289125.3(IFNAR2):c.971G>A (p.Ser324Asn)	IFNAR2, IFNAR2-IL10RB (S324N)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified +1 more	GUncertain significance
Select item 1460955	NM_001289125.3(IFNAR2):c.1000G>A (p.Gly334Ser)	IFNAR2, IFNAR2-IL10RB (G334S)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified +1 more	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)	not specified +1 more	GUncertain significance
Select item 1520823	NM_001289125.3(IFNAR2):c.1136C>T (p.Thr379Met)	IFNAR2, IFNAR2-IL10RB (T379M)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified +1 more	GConflicting classifications of pathogenicity
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)	not specified	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)	not specified	GUncertain significance
Select item 2190847	NM_001289125.3(IFNAR2):c.1310A>G (p.Asp437Gly)	IFNAR2, IFNAR2-IL10RB (D437G)	Single nucleotide variant (3 prime UTR variant +1 more)	not provided +1 more	GUncertain significance
Select item 3108285	NM_001289125.3(IFNAR2):c.1324G>A (p.Asp442Asn)	IFNAR2, IFNAR2-IL10RB (D442N)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 1992124	NM_001289125.3(IFNAR2):c.1411C>A (p.Leu471Met)	IFNAR2, IFNAR2-IL10RB (L471M)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified +1 more	GUncertain significance
Select item 3108286	NM_001289125.3(IFNAR2):c.1444C>T (p.Pro482Ser)	IFNAR2, IFNAR2-IL10RB (P482S)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	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)	not provided +1 more	GUncertain significance

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Items: 32