"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "IFNAR2-IL10RB" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1693767	NM_000628.5(IL10RB):c.130G>A (p.Ala44Thr)	IFNAR2-IL10RB, IL10RB (A44T)	Single nucleotide variant (missense variant)	not provided	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 +2 more	GUncertain significance
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 576700	NM_000628.5(IL10RB):c.727G>T (p.Ala243Ser)	IFNAR2-IL10RB, IL10RB (A243S)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 339695	NM_000628.5(IL10RB):c.727G>A (p.Ala243Thr)	IFNAR2-IL10RB, IL10RB (A243T)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 935606	NM_000628.5(IL10RB):c.946G>A (p.Gly316Arg)	IL10RB, IFNAR2-IL10RB (G316R)	Single nucleotide variant (missense variant)	Inflammatory bowel disease 25 +1 more	GUncertain significance
Select item 835048	NM_000628.5(IL10RB):c.953C>T (p.Pro318Leu)	IFNAR2-IL10RB, IL10RB (P318L)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance

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