ClinVar for MedGen (Select 393403) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3248153	NC_000021.8:g.(?_34638771)_(34668662_?)del	IL10RB	Deletion	Inflammatory bowel disease 25	GPathogenic
Select item 3017067	NM_000628.5(IL10RB):c.647-17C>T	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (intron variant)	Inflammatory bowel disease 25	GLikely benign
Select item 3015115	NM_000628.5(IL10RB):c.549A>G (p.Pro183=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant +1 more)	Inflammatory bowel disease 25	GLikely benign
Select item 2958691	NM_000628.5(IL10RB):c.144G>A (p.Gly48=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant +1 more)	Inflammatory bowel disease 25	GLikely benign
Select item 2958466	NM_000628.5(IL10RB):c.759G>A (p.Lys253=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant +2 more)	Inflammatory bowel disease 25	GLikely benign
Select item 2958017	NM_000628.5(IL10RB):c.52T>C (p.Leu18=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant +1 more)	Inflammatory bowel disease 25	GLikely benign
Select item 2917774	NM_000628.5(IL10RB):c.594G>A (p.Arg198=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant +1 more)	Inflammatory bowel disease 25	GLikely benign
Select item 2905671	NM_000628.5(IL10RB):c.555A>G (p.Thr185=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant +1 more)	Inflammatory bowel disease 25	GLikely benign
Select item 2903143	NM_000628.5(IL10RB):c.498+19A>G	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (intron variant)	Inflammatory bowel disease 25	GLikely benign
Select item 2893118	NM_000628.5(IL10RB):c.27G>A (p.Leu9=)	IFNAR2-IL10RB, IL10RB +1 more	Single nucleotide variant (synonymous variant +2 more)	Inflammatory bowel disease 25	GLikely benign
Select item 2891335	NM_000628.5(IL10RB):c.849T>C (p.Phe283=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant +2 more)	Inflammatory bowel disease 25	GLikely benign
Select item 2878924	NM_000628.5(IL10RB):c.796C>T (p.Leu266=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant +2 more)	Inflammatory bowel disease 25	GLikely benign
Select item 2873858	NM_000628.5(IL10RB):c.372T>G (p.Ala124=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant +1 more)	Inflammatory bowel disease 25	GLikely benign
Select item 2844597	NM_000628.5(IL10RB):c.831A>G (p.Thr277=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant +2 more)	Inflammatory bowel disease 25	GLikely benign
Select item 2833353	NM_000628.5(IL10RB):c.834T>A (p.Leu278=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant +2 more)	Inflammatory bowel disease 25	GLikely benign
Select item 2821919	NM_000628.5(IL10RB):c.804+12G>A	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (intron variant)	Inflammatory bowel disease 25	GLikely benign
Select item 2799559	NM_000628.5(IL10RB):c.691G>A (p.Val231Ile)	IFNAR2-IL10RB, IL10RB (V451I +1 more)	Single nucleotide variant (missense variant +2 more)	Inflammatory bowel disease 25	GUncertain significance
Select item 2792052	NM_000628.5(IL10RB):c.561T>C (p.Tyr187=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant +1 more)	Inflammatory bowel disease 25	GLikely benign
Select item 2761588	NM_000628.5(IL10RB):c.498G>A (p.Lys166=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant +1 more)	Inflammatory bowel disease 25	GUncertain significance
Select item 2742376	NM_000628.5(IL10RB):c.332-17del	IFNAR2-IL10RB, IL10RB	Deletion (intron variant)	Inflammatory bowel disease 25	GLikely benign
Select item 2721535	NM_000628.5(IL10RB):c.945C>T (p.Leu315=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant +2 more)	Inflammatory bowel disease 25	GLikely benign
Select item 2717297	NM_000628.5(IL10RB):c.40C>T (p.Leu14=)	IFNAR2-IL10RB, IL10RB +1 more	Single nucleotide variant (synonymous variant +2 more)	Inflammatory bowel disease 25	GLikely benign
Select item 2702144	NM_000628.5(IL10RB):c.702C>T (p.Val234=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant +2 more)	Inflammatory bowel disease 25	GLikely benign
Select item 2699058	NM_000628.5(IL10RB):c.174-1G>A	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (splice acceptor variant)	Inflammatory bowel disease 25	GLikely pathogenic
Select item 2664350	NM_000628.5(IL10RB):c.25_43del (p.Leu9fs)	IFNAR2-IL10RB, IL10RB +1 more (L9fs)	Deletion (frameshift variant +2 more)	Inflammatory bowel disease 25	GLikely pathogenic
Select item 2664348	NM_000628.5(IL10RB):c.300G>A (p.Trp100Ter)	IFNAR2-IL10RB, IL10RB (W100* +1 more)	Single nucleotide variant (nonsense)	Inflammatory bowel disease 25	GPathogenic
Select item 2500044	NM_000628.5(IL10RB):c.435G>A (p.Met145Ile)	IFNAR2-IL10RB, IL10RB (M145I +1 more)	Single nucleotide variant (missense variant +1 more)	Hepatitis B virus, susceptibility to +1 more	GUncertain significance
Select item 2431391	NM_000628.5(IL10RB):c.787C>G (p.Pro263Ala)	IFNAR2-IL10RB, IL10RB (P263A +1 more)	Single nucleotide variant (missense variant +2 more)	Inflammatory bowel disease 25	GUncertain significance
Select item 2427923	NM_000628.5(IL10RB):c.150G>A (p.Leu50=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant +1 more)	Inflammatory bowel disease 25	GLikely benign
Select item 2423333	NC_000021.8:g.(?_34668469)_(34668662_?)dup	IL10RB	Duplication	Inflammatory bowel disease 25	GUncertain significance
Select item 2423332	NC_000021.8:g.(?_34648881)_(34655566_?)del	IL10RB	Deletion	Inflammatory bowel disease 25	GPathogenic
Select item 2202006	NM_000628.5(IL10RB):c.912C>T (p.Ser304=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant +2 more)	Inflammatory bowel disease 25	GLikely benign
Select item 2195582	NM_000628.5(IL10RB):c.584T>C (p.Leu195Pro)	IFNAR2-IL10RB, IL10RB (L195P +1 more)	Single nucleotide variant (missense variant +1 more)	Inflammatory bowel disease 25	GUncertain significance
Select item 2190198	NM_000628.5(IL10RB):c.741C>T (p.Cys247=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant +2 more)	Inflammatory bowel disease 25	GLikely benign
Select item 2183609	NM_000628.5(IL10RB):c.636A>C (p.Thr212=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant +1 more)	Inflammatory bowel disease 25	GLikely benign
Select item 2183608	NM_000628.5(IL10RB):c.568C>G (p.Gln190Glu)	IFNAR2-IL10RB, IL10RB (Q190E +1 more)	Single nucleotide variant (missense variant +1 more)	Inflammatory bowel disease 25	GUncertain significance
Select item 2156380	NM_000628.5(IL10RB):c.50-20T>C	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (intron variant)	Inflammatory bowel disease 25	GLikely benign
Select item 2135051	NM_000628.5(IL10RB):c.1A>T (p.Met1Leu)	IFNAR2-IL10RB, IL10RB +1 more (M1L)	Single nucleotide variant (missense variant +1 more)	Inflammatory bowel disease 25	GUncertain significance
Select item 2134483	NM_000628.5(IL10RB):c.726C>T (p.Phe242=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant +2 more)	Inflammatory bowel disease 25	GLikely benign
Select item 2123569	NM_000628.5(IL10RB):c.332-7del	IFNAR2-IL10RB, IL10RB	Deletion (intron variant)	Inflammatory bowel disease 25	GLikely benign
Select item 2112335	NM_000628.5(IL10RB):c.466G>A (p.Val156Met)	IFNAR2-IL10RB, IL10RB (V376M +1 more)	Single nucleotide variant (missense variant +1 more)	Inflammatory bowel disease 25	GUncertain significance
Select item 2108931	NM_000628.5(IL10RB):c.646+19C>T	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (intron variant)	Inflammatory bowel disease 25	GLikely benign
Select item 2100543	NM_000628.5(IL10RB):c.331+4A>T	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (intron variant)	Inflammatory bowel disease 25	GUncertain significance
Select item 2097290	NM_000628.5(IL10RB):c.833T>C (p.Leu278Pro)	IFNAR2-IL10RB, IL10RB (L498P +1 more)	Single nucleotide variant (missense variant +2 more)	Inflammatory bowel disease 25	GUncertain significance
Select item 2094746	NM_000628.5(IL10RB):c.5C>T (p.Ala2Val)	IFNAR2-IL10RB, IL10RB +1 more (A2V)	Single nucleotide variant (missense variant)	Inflammatory bowel disease 25	GUncertain significance
Select item 2092210	NM_000628.5(IL10RB):c.863A>T (p.Glu288Val)	IFNAR2-IL10RB, IL10RB (E288V +1 more)	Single nucleotide variant (missense variant +2 more)	Inflammatory bowel disease 25	GUncertain significance
Select item 2088574	NM_000628.5(IL10RB):c.660C>G (p.Ser220=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant +2 more)	Inflammatory bowel disease 25	GLikely benign
Select item 2088152	NM_000628.5(IL10RB):c.971A>G (p.Gln324Arg)	IFNAR2-IL10RB, IL10RB (Q324R +1 more)	Single nucleotide variant (missense variant +2 more)	Inflammatory bowel disease 25	GUncertain significance
Select item 2087685	NM_000628.5(IL10RB):c.29G>C (p.Gly10Ala)	IFNAR2-IL10RB, IL10RB +1 more (G10A)	Single nucleotide variant (missense variant)	Inflammatory bowel disease 25	GUncertain significance
Select item 2083967	NM_000628.5(IL10RB):c.138C>T (p.Ala46=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant +1 more)	Inflammatory bowel disease 25	GLikely benign
Select item 2069918	NM_000628.5(IL10RB):c.116A>G (p.Gln39Arg)	IFNAR2-IL10RB, IL10RB (Q39R +1 more)	Single nucleotide variant (missense variant +1 more)	Inflammatory bowel disease 25	GUncertain significance
Select item 2065685	NM_000628.5(IL10RB):c.444G>A (p.Val148=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant +1 more)	Inflammatory bowel disease 25	GLikely benign
Select item 2061188	NM_000628.5(IL10RB):c.598A>G (p.Lys200Glu)	IFNAR2-IL10RB, IL10RB (K200E +1 more)	Single nucleotide variant (missense variant +1 more)	Inflammatory bowel disease 25	GUncertain significance
Select item 2060643	NM_000628.5(IL10RB):c.444G>C (p.Val148=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant +1 more)	Inflammatory bowel disease 25	GLikely benign
Select item 2060034	NM_000628.5(IL10RB):c.179G>C (p.Arg60Thr)	IFNAR2-IL10RB, IL10RB (R280T +1 more)	Single nucleotide variant (missense variant)	Inflammatory bowel disease 25	GUncertain significance
Select item 2054401	NM_000628.5(IL10RB):c.612G>T (p.Trp204Cys)	IFNAR2-IL10RB, IL10RB (W424C +1 more)	Single nucleotide variant (missense variant +1 more)	Inflammatory bowel disease 25	GUncertain significance
Select item 2046535	NM_000628.5(IL10RB):c.823C>T (p.His275Tyr)	IFNAR2-IL10RB, IL10RB (S222L +2 more)	Single nucleotide variant (missense variant +1 more)	Inflammatory bowel disease 25	GUncertain significance
Select item 2040903	NM_000628.5(IL10RB):c.383A>T (p.His128Leu)	IFNAR2-IL10RB, IL10RB (H348L +1 more)	Single nucleotide variant (missense variant +1 more)	Inflammatory bowel disease 25	GUncertain significance
Select item 2016506	NM_000628.5(IL10RB):c.646+14T>C	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (intron variant)	Inflammatory bowel disease 25	GLikely benign
Select item 2013502	NM_000628.5(IL10RB):c.51A>G (p.Ala17=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant +1 more)	Inflammatory bowel disease 25	GLikely benign
Select item 2010836	NM_000628.5(IL10RB):c.791A>G (p.Gln264Arg)	IFNAR2-IL10RB, IL10RB (Q484R +1 more)	Single nucleotide variant (missense variant +2 more)	Inflammatory bowel disease 25	GUncertain significance
Select item 2000573	NM_000628.5(IL10RB):c.377C>T (p.Ser126Phe)	IFNAR2-IL10RB, IL10RB (S126F +1 more)	Single nucleotide variant (missense variant +1 more)	Inflammatory bowel disease 25	GUncertain significance
Select item 1997537	NM_000628.5(IL10RB):c.301G>C (p.Val101Leu)	IFNAR2-IL10RB, IL10RB (V101L +1 more)	Single nucleotide variant (missense variant)	Inflammatory bowel disease 25	GUncertain significance
Select item 1995647	NM_000628.5(IL10RB):c.60G>A (p.Met20Ile)	IL10RB, IFNAR2-IL10RB (M240I +1 more)	Single nucleotide variant (missense variant +1 more)	Inflammatory bowel disease 25	GUncertain significance
Select item 1988129	NM_000628.5(IL10RB):c.50-15G>A	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (intron variant)	Inflammatory bowel disease 25	GLikely benign
Select item 1983716	NM_000628.5(IL10RB):c.672C>T (p.Ala224=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant +2 more)	Inflammatory bowel disease 25	GLikely benign
Select item 1981117	NM_000628.5(IL10RB):c.680T>A (p.Leu227His)	IFNAR2-IL10RB, IL10RB (L447H +1 more)	Single nucleotide variant (missense variant +2 more)	Inflammatory bowel disease 25	GUncertain significance
Select item 1969707	NM_000628.5(IL10RB):c.511C>T (p.Pro171Ser)	IFNAR2-IL10RB, IL10RB (P391S +1 more)	Single nucleotide variant (missense variant +1 more)	Inflammatory bowel disease 25	GUncertain significance
Select item 1966309	NM_000628.5(IL10RB):c.203A>T (p.Asn68Ile)	IFNAR2-IL10RB, IL10RB (N288I +1 more)	Single nucleotide variant (missense variant)	Inflammatory bowel disease 25	GUncertain significance
Select item 1937965	NM_000628.5(IL10RB):c.343C>A (p.Pro115Thr)	IFNAR2-IL10RB, IL10RB (P115T +1 more)	Single nucleotide variant (missense variant +1 more)	Inflammatory bowel disease 25	GUncertain significance
Select item 1923430	NM_000628.5(IL10RB):c.49+19G>A	IFNAR2-IL10RB, IL10RB +1 more	Single nucleotide variant (intron variant)	Inflammatory bowel disease 25	GLikely benign
Select item 1907310	NM_000628.5(IL10RB):c.450C>T (p.Asn150=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant +1 more)	Inflammatory bowel disease 25	GLikely benign
Select item 1906988	NM_000628.5(IL10RB):c.804+13G>A	IL10RB, IFNAR2-IL10RB	Single nucleotide variant (intron variant)	Inflammatory bowel disease 25	GLikely benign
Select item 1902999	NM_000628.5(IL10RB):c.651G>A (p.Thr217=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant +2 more)	Inflammatory bowel disease 25	GUncertain significance
Select item 1713470	NM_000628.5(IL10RB):c.284A>T (p.Asp95Val)	IFNAR2-IL10RB, IL10RB (D95V)	Single nucleotide variant (missense variant)	Inflammatory bowel disease 25	GUncertain significance
Select item 1674955	NM_000628.5(IL10RB):c.312C>T (p.Thr104=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant)	Inflammatory bowel disease 25	GLikely benign
Select item 1672252	NM_000628.5(IL10RB):c.27G>C (p.Leu9=)	IFNAR2-IL10RB, IL10RB +1 more	Single nucleotide variant (synonymous variant)	Inflammatory bowel disease 25	GLikely benign
Select item 1661557	NM_000628.5(IL10RB):c.332-5del	IFNAR2-IL10RB, IL10RB	Deletion (intron variant)	Inflammatory bowel disease 25	GLikely benign
Select item 1646951	NM_000628.5(IL10RB):c.647-16C>G	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (intron variant)	Inflammatory bowel disease 25	GLikely benign
Select item 1643363	NM_000628.5(IL10RB):c.39G>A (p.Leu13=)	IFNAR2-IL10RB, IL10RB +1 more	Single nucleotide variant (synonymous variant)	Inflammatory bowel disease 25	GLikely benign
Select item 1624334	NM_000628.5(IL10RB):c.735G>A (p.Leu245=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant)	Inflammatory bowel disease 25	GLikely benign
Select item 1611356	NM_000628.5(IL10RB):c.891C>T (p.Val297=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant)	Inflammatory bowel disease 25	GLikely benign
Select item 1598270	NM_000628.5(IL10RB):c.49+12G>A	IFNAR2-IL10RB, IL10RB +1 more	Single nucleotide variant (intron variant)	Inflammatory bowel disease 25	GLikely benign
Select item 1596080	NM_000628.5(IL10RB):c.360A>G (p.Val120=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant)	Inflammatory bowel disease 25	GLikely benign
Select item 1593696	NM_000628.5(IL10RB):c.647-7del	IFNAR2-IL10RB, IL10RB	Deletion (intron variant)	Inflammatory bowel disease 25	GBenign
Select item 1582501	NM_000628.5(IL10RB):c.966G>A (p.Gly322=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant)	Inflammatory bowel disease 25	GLikely benign
Select item 1568977	NM_000628.5(IL10RB):c.804+17G>A	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (intron variant)	Inflammatory bowel disease 25	GLikely benign
Select item 1567448	NM_000628.5(IL10RB):c.174-14T>C	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (intron variant)	Inflammatory bowel disease 25	GLikely benign
Select item 1564750	NM_000628.5(IL10RB):c.174-18A>G	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (intron variant)	Inflammatory bowel disease 25	GLikely benign
Select item 1556184	NM_000628.5(IL10RB):c.49+19G>T	IFNAR2-IL10RB, IL10RB +1 more	Single nucleotide variant (intron variant)	Inflammatory bowel disease 25	GLikely benign
Select item 1544512	NM_000628.5(IL10RB):c.332-11C>G	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (intron variant)	Inflammatory bowel disease 25	GLikely benign
Select item 1541429	NM_000628.5(IL10RB):c.388C>T (p.Arg130Cys)	IFNAR2-IL10RB, IL10RB (R130C)	Single nucleotide variant (missense variant)	Inflammatory bowel disease 25	GLikely benign
Select item 1528177	NM_000628.5(IL10RB):c.954G>A (p.Pro318=)	IFNAR2-IL10RB, IL10RB	Single nucleotide variant (synonymous variant)	Inflammatory bowel disease 25	GConflicting classifications of pathogenicity
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 1510814	NM_000628.5(IL10RB):c.302T>C (p.Val101Ala)	IFNAR2-IL10RB, IL10RB (V101A)	Single nucleotide variant (missense variant)	Inflammatory bowel disease 25	GUncertain significance
Select item 1503322	NM_000628.5(IL10RB):c.386T>G (p.Met129Arg)	IFNAR2-IL10RB, IL10RB (M129R)	Single nucleotide variant (missense variant)	Inflammatory bowel disease 25	GUncertain significance
Select item 1490999	NM_000628.5(IL10RB):c.641A>G (p.His214Arg)	IFNAR2-IL10RB, IL10RB (H214R)	Single nucleotide variant (missense variant)	Inflammatory bowel disease 25	GUncertain significance
Select item 1490134	NM_000628.5(IL10RB):c.274G>C (p.Glu92Gln)	IFNAR2-IL10RB, IL10RB (E92Q)	Single nucleotide variant (missense variant)	Inflammatory bowel disease 25	GUncertain significance
Select item 1489805	NM_000628.5(IL10RB):c.498G>C (p.Lys166Asn)	IFNAR2-IL10RB, IL10RB (K166N)	Single nucleotide variant (missense variant)	Inflammatory bowel disease 25	GUncertain significance
Select item 1486790	NM_000628.5(IL10RB):c.800_801del (p.Lys267fs)	IFNAR2-IL10RB, IL10RB (K267fs)	Deletion (frameshift variant)	Inflammatory bowel disease 25	GUncertain significance

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