"Ambry Genetics"[submitter] AND "IFNAR2-IL10RB"[gene] - ClinVar

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Items: 46

	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 specified +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)	not specified +1 more	GUncertain significance
Select item 1913560	NM_001289125.3(IFNAR2):c.122T>C (p.Phe41Ser)	IFNAR2-IL10RB, IFNAR2 (F41S)	Single nucleotide variant (missense variant)	not specified +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 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 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)	not specified +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 provided +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 provided +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
Select item 2303032	NM_000628.5(IL10RB):c.24G>T (p.Trp8Cys)	IFNAR2-IL10RB, IL10RB +1 more (W8C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1423543	NM_000628.5(IL10RB):c.85A>G (p.Met29Val)	IFNAR2-IL10RB, IL10RB (M29V)	Single nucleotide variant (missense variant)	Inflammatory bowel disease 25 +1 more	GUncertain significance
Select item 662220	NM_000628.5(IL10RB):c.328G>A (p.Asp110Asn)	IFNAR2-IL10RB, IL10RB (D110N)	Single nucleotide variant (missense variant)	Inflammatory bowel disease 25 +1 more	GUncertain significance
Select item 2387706	NM_000628.5(IL10RB):c.385A>G (p.Met129Val)	IFNAR2-IL10RB, IL10RB (M349V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 537181	NM_000628.5(IL10RB):c.446A>G (p.Tyr149Cys)	IFNAR2-IL10RB, IL10RB (Y149C)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 339694	NM_000628.5(IL10RB):c.484G>A (p.Gly162Ser)	IFNAR2-IL10RB, IL10RB (G162S)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 955970	NM_000628.5(IL10RB):c.548C>G (p.Pro183Arg)	IFNAR2-IL10RB, IL10RB (P183R)	Single nucleotide variant (missense variant)	Inflammatory bowel disease 25 +1 more	GUncertain significance
Select item 520905	NM_000628.5(IL10RB):c.562T>G (p.Cys188Gly)	IFNAR2-IL10RB, IL10RB (C188G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3109054	NM_000628.5(IL10RB):c.571G>A (p.Val191Ile)	IFNAR2-IL10RB, IL10RB (V191I +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1047787	NM_000628.5(IL10RB):c.593G>A (p.Arg198Gln)	IFNAR2-IL10RB, IL10RB (R198Q)	Single nucleotide variant (missense variant)	Inflammatory bowel disease 25 +1 more	GUncertain significance
Select item 2624130	NM_000628.5(IL10RB):c.665T>C (p.Met222Thr)	IFNAR2-IL10RB, IL10RB (M222T +1 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 1518715	NM_000628.5(IL10RB):c.673G>A (p.Val225Ile)	IFNAR2-IL10RB, IL10RB (V225I)	Single nucleotide variant (missense variant)	Inflammatory bowel disease 25 +1 more	GConflicting classifications of pathogenicity
Select item 566702	NM_000628.5(IL10RB):c.718G>A (p.Gly240Ser)	IFNAR2-IL10RB, IL10RB (G240S)	Single nucleotide variant (missense variant)	Inflammatory bowel disease 25 +2 more	GUncertain significance
Select item 576932	NM_000628.5(IL10RB):c.742G>A (p.Val248Ile)	IFNAR2-IL10RB, IL10RB (V248I)	Single nucleotide variant (missense variant)	Inflammatory bowel disease 25 +1 more	GConflicting classifications of pathogenicity
Select item 577689	NM_000628.5(IL10RB):c.911G>A (p.Ser304Asn)	IFNAR2-IL10RB, IL10RB (S304N)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 537182	NM_000628.5(IL10RB):c.913G>A (p.Gly305Ser)	IFNAR2-IL10RB, IL10RB (G305S)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity

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Items: 46