C2675508[trait identifier] AND "Illumina Laboratory Services, Illumina - ClinVar

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Items: 32

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 339688	NM_000628.5(IL10RB):c.-94C>A	IFNAR2-IL10RB, IL10RB +1 more	Single nucleotide variant (5 prime UTR variant)	Inflammatory bowel disease 25	GUncertain significance
Select item 339689	NM_000628.5(IL10RB):c.-74C>A	IFNAR2-IL10RB, IL10RB +1 more	Single nucleotide variant (5 prime UTR variant)	Inflammatory bowel disease 25	GUncertain significance
Select item 339690	NM_000628.5(IL10RB):c.-72C>A	LOC130066558, IFNAR2-IL10RB +1 more	Single nucleotide variant (5 prime UTR variant)	Inflammatory bowel disease 25	GLikely benign
Select item 899242	NM_000628.5(IL10RB):c.-66A>T	IFNAR2-IL10RB, IL10RB +1 more	Single nucleotide variant (5 prime UTR variant)	Inflammatory bowel disease 25	GUncertain significance
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 16923	NM_000628.5(IL10RB):c.139A>G (p.Lys47Glu)	IFNAR2-IL10RB, IL10RB (K47E)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign
Select item 339693	NM_000628.5(IL10RB):c.174-14T>G	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (intron variant)	Inflammatory bowel disease 25	GConflicting classifications of pathogenicity
Select item 895130	NM_000628.5(IL10RB):c.332-11C>T	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (intron variant)	Inflammatory bowel disease 25	GConflicting classifications of pathogenicity
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 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 631881	NM_000628.5(IL10RB):c.611G>A (p.Trp204Ter)	IFNAR2-IL10RB, IL10RB (W204*)	Single nucleotide variant (nonsense)	Inflammatory bowel disease 25	GPathogenic/Likely pathogenic
Select item 742180	NM_000628.5(IL10RB):c.645C>T (p.Asp215=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant)	Inflammatory bowel disease 25	GConflicting classifications of pathogenicity
Select item 568167	NM_000628.5(IL10RB):c.646G>A (p.Glu216Lys)	IFNAR2-IL10RB, IL10RB (E216K)	Single nucleotide variant (missense variant)	Inflammatory bowel disease 25 +1 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 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 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 339696	NM_000628.5(IL10RB):c.*17A>G	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (3 prime UTR variant)	Inflammatory bowel disease 25	GUncertain significance
Select item 339697	NM_000628.5(IL10RB):c.*20C>T	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (3 prime UTR variant)	Inflammatory bowel disease 25	GUncertain significance
Select item 339698	NM_000628.5(IL10RB):c.*85A>G	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (3 prime UTR variant)	not specified +1 more	GBenign
Select item 339699	NM_000628.5(IL10RB):c.*135G>A	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (3 prime UTR variant)	Inflammatory bowel disease 25	GBenign
Select item 339700	NM_000628.5(IL10RB):c.*314G>A	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (3 prime UTR variant)	Inflammatory bowel disease 25	GBenign
Select item 339701	NM_000628.5(IL10RB):c.*334G>A	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (3 prime UTR variant)	Inflammatory bowel disease 25	GBenign
Select item 339703	NM_000628.5(IL10RB):c.*515C>T	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (3 prime UTR variant)	Inflammatory bowel disease 25	GUncertain significance
Select item 898189	NM_000628.5(IL10RB):c.*519A>G	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (3 prime UTR variant)	Inflammatory bowel disease 25	GUncertain significance
Select item 898190	NM_000628.5(IL10RB):c.*536G>T	IL10RB, IFNAR2-IL10RB	Single nucleotide variant (3 prime UTR variant)	Inflammatory bowel disease 25	GUncertain significance
Select item 339704	NM_000628.5(IL10RB):c.*546G>A	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (3 prime UTR variant)	Inflammatory bowel disease 25	GUncertain significance
Select item 339708	NM_000628.5(IL10RB):c.*616A>G	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (3 prime UTR variant)	Inflammatory bowel disease 25	GUncertain significance
Select item 339709	NM_000628.5(IL10RB):c.*719G>A	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (3 prime UTR variant)	Inflammatory bowel disease 25	GBenign
Select item 339710	NM_000628.5(IL10RB):c.*761C>T	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (3 prime UTR variant)	Inflammatory bowel disease 25	GUncertain significance
Select item 339711	NM_000628.5(IL10RB):c.*796T>C	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (3 prime UTR variant)	Inflammatory bowel disease 25	GUncertain significance
Select item 339712	NM_000628.5(IL10RB):c.*816T>C	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (3 prime UTR variant)	Inflammatory bowel disease 25	GUncertain significance

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Items: 32