"PreventionGenetics, part of Exact Sciences"[submitter] AND "IFNAR2-IL - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1453685	NM_001289125.3(IFNAR2):c.369A>G (p.Ser123=)	IFNAR2, IFNAR2-IL10RB	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1123923	NM_001289125.3(IFNAR2):c.591T>C (p.Ile197=)	IFNAR2, IFNAR2-IL10RB	Single nucleotide variant (synonymous variant)	IFNAR2-related condition +1 more	GLikely benign
Select item 3050340	NM_001289125.3(IFNAR2):c.838T>C (p.Leu280=)	IFNAR2, IFNAR2-IL10RB	Single nucleotide variant (intron variant +1 more)	IFNAR2-related condition	GLikely benign
Select item 3029025	NM_001289125.3(IFNAR2):c.960T>C (p.Asp320=)	IFNAR2, IFNAR2-IL10RB	Single nucleotide variant (3 prime UTR variant +2 more)	IFNAR2-related condition	GLikely benign
Select item 1165291	NM_001289125.3(IFNAR2):c.1092C>T (p.Ser364=)	IFNAR2, IFNAR2-IL10RB	Single nucleotide variant (3 prime UTR variant +1 more)	IFNAR2-related condition +1 more	GBenign
Select item 1165918	NM_001289125.3(IFNAR2):c.1152C>T (p.Ser384=)	IFNAR2, IFNAR2-IL10RB	Single nucleotide variant (3 prime UTR variant +1 more)	not provided +1 more	GBenign
Select item 1593239	NM_001289125.3(IFNAR2):c.1221C>T (p.Pro407=)	IFNAR2, IFNAR2-IL10RB	Single nucleotide variant (3 prime UTR variant +1 more)	not provided +1 more	GLikely benign
Select item 1110578	NM_000628.5(IL10RB):c.49+8G>T	IFNAR2-IL10RB, IL10RB +1 more	Single nucleotide variant (intron variant)	IL10RB-related condition +1 more	GLikely benign
Select item 339691	NM_000628.5(IL10RB):c.73G>A (p.Glu25Lys)	IFNAR2-IL10RB, IL10RB (E25K)	Single nucleotide variant (missense variant)	IL10RB-related condition +1 more	GBenign/Likely benign
Select item 339692	NM_000628.5(IL10RB):c.131C>T (p.Ala44Val)	IFNAR2-IL10RB, IL10RB (A44V)	Single nucleotide variant (missense variant)	IL10RB-related condition +1 more	GBenign/Likely benign
Select item 537180	NM_000628.5(IL10RB):c.442G>A (p.Val148Met)	IFNAR2-IL10RB, IL10RB (V148M)	Single nucleotide variant (missense variant)	IL10RB-related condition +2 more	GConflicting classifications of pathogenicity
Select item 719016	NM_000628.5(IL10RB):c.483C>T (p.Asn161=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant)	IL10RB-related condition +1 more	GBenign/Likely benign
Select item 3053660	NM_000628.5(IL10RB):c.588T>C (p.Pro196=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant +1 more)	IL10RB-related condition	GLikely benign
Select item 576700	NM_000628.5(IL10RB):c.727G>T (p.Ala243Ser)	IFNAR2-IL10RB, IL10RB (A243S)	Single nucleotide variant (missense variant)	Inflammatory bowel disease 25 +2 more	GConflicting classifications of pathogenicity
Select item 733200	NM_000628.5(IL10RB):c.763G>A (p.Ala255Thr)	IL10RB, IFNAR2-IL10RB (A255T)	Single nucleotide variant (missense variant)	IL10RB-related condition +1 more	GConflicting classifications of pathogenicity
Select item 992564	NM_000628.5(IL10RB):c.804+8G>A	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (intron variant)	IL10RB-related condition +2 more	GConflicting classifications of pathogenicity