"Ambry Genetics"[submitter] AND "IL6ST"[gene] - ClinVar

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Items: 40

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1519246	NM_002184.4(IL6ST):c.2618C>T (p.Ala873Val)	IL6ST (A541V +6 more)	Single nucleotide variant (missense variant +2 more)	not specified +1 more	GUncertain significance
Select item 1492250	NM_002184.4(IL6ST):c.2563C>A (p.His855Asn)	IL6ST (H523N +6 more)	Single nucleotide variant (missense variant +2 more)	not specified +1 more	GUncertain significance
Select item 2488848	NM_002184.4(IL6ST):c.2474G>A (p.Ser825Asn)	IL6ST (S536N +6 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2970121	NM_002184.4(IL6ST):c.2315C>T (p.Pro772Leu)	IL6ST (P471L +6 more)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GUncertain significance
Select item 2051022	NM_002184.4(IL6ST):c.2284G>A (p.Val762Met)	IL6ST (V430M +6 more)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GUncertain significance
Select item 2252351	NM_002184.4(IL6ST):c.2228G>A (p.Ser743Asn)	IL6ST (S411N +6 more)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GUncertain significance
Select item 1404918	NM_002184.4(IL6ST):c.2121T>G (p.Asp707Glu)	IL6ST (D673E +6 more)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GUncertain significance
Select item 3285907	NM_002184.4(IL6ST):c.2093C>A (p.Ala698Glu)	IL6ST (A397E +6 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2254927	NM_002184.4(IL6ST):c.2071G>A (p.Val691Ile)	IL6ST (V657I +6 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 1441425	NM_002184.4(IL6ST):c.2045T>C (p.Met682Thr)	IL6ST (M381T +6 more)	Single nucleotide variant (missense variant +2 more)	not specified +1 more	GUncertain significance
Select item 1448598	NM_002184.4(IL6ST):c.2023A>G (p.Asn675Asp)	IL6ST (N343D +6 more)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GUncertain significance
Select item 2286675	NM_002184.4(IL6ST):c.2017A>G (p.Arg673Gly)	IL6ST (R384G +6 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 1381681	NM_002184.4(IL6ST):c.1925A>G (p.Asn642Ser)	IL6ST (N310S +6 more)	Single nucleotide variant (missense variant +2 more)	not specified +1 more	GUncertain significance
Select item 3109464	NM_002184.4(IL6ST):c.1799G>T (p.Gly600Val)	IL6ST (G530V +6 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 1953856	NM_002184.4(IL6ST):c.1600G>A (p.Glu534Lys)	IL6ST (E245K +6 more)	Single nucleotide variant (missense variant +2 more)	not specified +1 more	GUncertain significance
Select item 2477894	NM_002184.4(IL6ST):c.1562A>G (p.Lys521Arg)	IL6ST (K189R +6 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2612551	NM_002184.4(IL6ST):c.1559C>G (p.Ser520Cys)	IL6ST (S188C +6 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2175010	NM_002184.4(IL6ST):c.1528A>G (p.Ile510Val)	IL6ST (I449V +5 more)	Single nucleotide variant (missense variant +3 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3285906	NM_002184.4(IL6ST):c.1511C>T (p.Pro504Leu)	IL6ST (P504L +5 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2250040	NM_002184.4(IL6ST):c.1444T>A (p.Leu482Ile)	IL6ST (L412I +4 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 1449332	NM_002184.4(IL6ST):c.1429G>A (p.Val477Met)	IL6ST (V176M +4 more)	Single nucleotide variant (missense variant +3 more)	not specified +1 more	GUncertain significance
Select item 2617003	NM_002184.4(IL6ST):c.1330A>G (p.Thr444Ala)	IL6ST (T143A +4 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2621809	NM_002184.4(IL6ST):c.1184G>A (p.Arg395His)	IL6ST (R325H +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2788931	NM_002184.4(IL6ST):c.1097A>G (p.Tyr366Cys)	IL6ST (Y366C +4 more)	Single nucleotide variant (missense variant +2 more)	not specified +1 more	GUncertain significance
Select item 1651210	NM_002184.4(IL6ST):c.1064C>T (p.Pro355Leu)	IL6ST (P23L +4 more)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2265916	NM_002184.4(IL6ST):c.941G>C (p.Ser314Thr)	IL6ST (S244T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1385577	NM_002184.4(IL6ST):c.875T>C (p.Phe292Ser)	IL6ST (F222S +1 more)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GUncertain significance
Select item 1938697	NM_002184.4(IL6ST):c.820C>G (p.Pro274Ala)	IL6ST (P204A +1 more)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GUncertain significance
Select item 2253538	NM_002184.4(IL6ST):c.770A>G (p.Tyr257Cys)	IL6ST (Y187C +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 1505545	NM_002184.4(IL6ST):c.649G>C (p.Val217Leu)	IL6ST (V147L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified +1 more	GUncertain significance
Select item 2333957	NM_002184.4(IL6ST):c.632A>C (p.His211Pro)	IL6ST (H141P +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2544155	NM_002184.4(IL6ST):c.617A>G (p.Lys206Arg)	IL6ST (K206R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2548253	NM_002184.4(IL6ST):c.501C>G (p.His167Gln)	IL6ST (H167Q +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2376414	NM_002184.4(IL6ST):c.301C>T (p.Leu101Phe)	IL6ST (L101F)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2309758	NM_002184.4(IL6ST):c.289T>A (p.Leu97Ile)	IL6ST (L97I)	Single nucleotide variant (missense variant +3 more)	not provided +1 more	GUncertain significance
Select item 2525450	NM_002184.4(IL6ST):c.282A>G (p.Ile94Met)	IL6ST (I94M)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2613909	NM_002184.4(IL6ST):c.281T>G (p.Ile94Arg)	IL6ST (I94R)	Single nucleotide variant (missense variant +3 more)	not provided +1 more	GUncertain significance
Select item 2064040	NM_002184.4(IL6ST):c.191A>G (p.Tyr64Cys)	IL6ST (Y64C)	Single nucleotide variant (missense variant +3 more)	not provided +1 more	GUncertain significance
Select item 2271846	NM_002184.4(IL6ST):c.80C>A (p.Pro27Gln)	IL6ST (P27Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2182861	NM_002184.4(IL6ST):c.52A>G (p.Thr18Ala)	IL6ST (T18A)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GUncertain significance

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Items: 40