Related gene-specific medical variations for Gene (Select 4820) - ClinVar

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Links from Gene

Items: 76

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3299901	NM_005385.4(NKTR):c.1478A>T (p.His493Leu)	NKTR, ZBTB47-AS1 (H125L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299900	NM_005385.4(NKTR):c.3557A>G (p.Lys1186Arg)	NKTR, ZBTB47-AS1 (K818R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299898	NM_005385.4(NKTR):c.205A>G (p.Lys69Glu)	NKTR, ZBTB47-AS1 (K69E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3299897	NM_005385.4(NKTR):c.1044A>T (p.Arg348Ser)	NKTR, ZBTB47-AS1 (R95S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3299896	NM_005385.4(NKTR):c.1955T>C (p.Leu652Ser)	NKTR, ZBTB47-AS1 (L284S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299895	NM_005385.4(NKTR):c.3515A>C (p.Gln1172Pro)	NKTR, ZBTB47-AS1 (Q919P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299894	NM_005385.4(NKTR):c.526C>T (p.Leu176Phe)	NKTR, ZBTB47-AS1 (L176F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3299893	NM_005385.4(NKTR):c.3308C>T (p.Ala1103Val)	NKTR, ZBTB47-AS1 (A1103V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299892	NM_005385.4(NKTR):c.2678G>A (p.Arg893Gln)	NKTR, ZBTB47-AS1 (R525Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299891	NM_005385.4(NKTR):c.1187G>A (p.Arg396Gln)	NKTR, ZBTB47-AS1 (R143Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299890	NM_005385.4(NKTR):c.2753C>G (p.Ser918Cys)	NKTR, ZBTB47-AS1 (S665C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200337	NM_005385.4(NKTR):c.914C>T (p.Thr305Ile)	NKTR, ZBTB47-AS1 (T305I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200336	NM_005385.4(NKTR):c.701G>A (p.Arg234His)	NKTR, ZBTB47-AS1 (R234H)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3200335	NM_005385.4(NKTR):c.3991T>G (p.Ser1331Ala)	NKTR, ZBTB47-AS1 (S1078A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200333	NM_005385.4(NKTR):c.2686A>C (p.Thr896Pro)	NKTR, ZBTB47-AS1 (T643P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200332	NM_005385.4(NKTR):c.2302G>A (p.Val768Ile)	NKTR, ZBTB47-AS1 (V400I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200331	NM_005385.4(NKTR):c.2233A>G (p.Thr745Ala)	NKTR, ZBTB47-AS1 (T492A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200330	NM_005385.4(NKTR):c.1988C>T (p.Ser663Phe)	NKTR, ZBTB47-AS1 (S295F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200329	NM_005385.4(NKTR):c.1940A>G (p.Gln647Arg)	NKTR, ZBTB47-AS1 (Q394R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200326	NM_005385.4(NKTR):c.1117A>G (p.Arg373Gly)	NKTR, ZBTB47-AS1 (R373G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620718	NM_005385.4(NKTR):c.1954T>G (p.Leu652Val)	NKTR, ZBTB47-AS1 (L284V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2609937	NM_005385.4(NKTR):c.1556A>G (p.Tyr519Cys)	NKTR, ZBTB47-AS1 (Y151C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607941	NM_005385.4(NKTR):c.3406A>T (p.Arg1136Trp)	NKTR, ZBTB47-AS1 (R1136W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607110	NM_005385.4(NKTR):c.2927A>T (p.Lys976Met)	NKTR, ZBTB47-AS1 (K976M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602130	NM_005385.4(NKTR):c.2551C>G (p.Arg851Gly)	LOC129936565, NKTR +1 more (R483G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591268	NM_005385.4(NKTR):c.1936A>G (p.Ile646Val)	NKTR, ZBTB47-AS1 (I393V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591053	NM_005385.4(NKTR):c.4005T>G (p.Ser1335Arg)	NKTR, ZBTB47-AS1 (S967R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2561278	NM_005385.4(NKTR):c.3694G>A (p.Val1232Met)	NKTR, ZBTB47-AS1 (V979M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2559810	NM_005385.4(NKTR):c.3110A>G (p.Gln1037Arg)	NKTR, ZBTB47-AS1 (Q1037R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554095	NM_005385.4(NKTR):c.1120G>A (p.Ala374Thr)	NKTR, ZBTB47-AS1 (A121T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553509	NM_005385.4(NKTR):c.3182C>T (p.Ser1061Phe)	NKTR, ZBTB47-AS1 (S808F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553310	NM_005385.4(NKTR):c.2984A>G (p.Glu995Gly)	NKTR, ZBTB47-AS1 (E742G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538398	NM_005385.4(NKTR):c.3154A>G (p.Lys1052Glu)	NKTR, ZBTB47-AS1 (K799E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537539	NM_005385.4(NKTR):c.187A>T (p.Thr63Ser)	NKTR, ZBTB47-AS1 (T63S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2532324	NM_005385.4(NKTR):c.341G>A (p.Arg114Gln)	NKTR, ZBTB47-AS1 (R114Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2524011	NM_005385.4(NKTR):c.1235A>G (p.Asn412Ser)	NKTR, ZBTB47-AS1 (N412S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512739	NM_005385.4(NKTR):c.8C>T (p.Ala3Val)	NKTR, SEC22C (A3V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2507979	NM_005385.4(NKTR):c.2813A>G (p.Asn938Ser)	NKTR, ZBTB47-AS1 (N570S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476234	NM_005385.4(NKTR):c.3470A>T (p.Asp1157Val)	NKTR, ZBTB47-AS1 (D1157V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469344	NM_005385.4(NKTR):c.1802T>C (p.Val601Ala)	NKTR, ZBTB47-AS1 (V601A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467922	NM_005385.4(NKTR):c.2879C>G (p.Ser960Cys)	LOC129936566, NKTR +1 more (S707C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411315	NM_005385.4(NKTR):c.1439A>G (p.Asp480Gly)	NKTR, ZBTB47-AS1 (D112G +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2409252	NM_005385.4(NKTR):c.1328A>G (p.Lys443Arg)	NKTR, ZBTB47-AS1 (K190R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404898	NM_005385.4(NKTR):c.2420A>G (p.Tyr807Cys)	LOC129936565, NKTR +1 more (Y439C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402669	NM_005385.4(NKTR):c.1456C>T (p.Arg486Cys)	NKTR, ZBTB47-AS1 (R233C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401723	NM_005385.4(NKTR):c.3817C>T (p.Arg1273Trp)	NKTR, ZBTB47-AS1 (R1273W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399829	NM_005385.4(NKTR):c.2009A>G (p.Asn670Ser)	NKTR, ZBTB47-AS1 (N670S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386284	NM_005385.4(NKTR):c.3377A>G (p.Asp1126Gly)	NKTR, ZBTB47-AS1 (D1126G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383532	NM_005385.4(NKTR):c.3865C>T (p.Arg1289Cys)	NKTR, ZBTB47-AS1 (R1289C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381217	NM_005385.4(NKTR):c.2905A>G (p.Asn969Asp)	LOC129936566, NKTR +1 more (N969D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380915	NM_005385.4(NKTR):c.4109G>A (p.Arg1370Gln)	NKTR, ZBTB47-AS1 (R1002Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375214	NM_005385.4(NKTR):c.1382T>C (p.Ile461Thr)	NKTR, ZBTB47-AS1 (I208T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372038	NM_005385.4(NKTR):c.4070G>A (p.Arg1357Gln)	NKTR, ZBTB47-AS1 (R1104Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358234	NM_005385.4(NKTR):c.3455G>A (p.Arg1152Gln)	NKTR, ZBTB47-AS1 (R1152Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356898	NM_005385.4(NKTR):c.1298A>C (p.Glu433Ala)	NKTR, ZBTB47-AS1 (E433A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339652	NM_005385.4(NKTR):c.1547G>A (p.Arg516Lys)	NKTR, ZBTB47-AS1 (R148K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338434	NM_005385.4(NKTR):c.614C>T (p.Ser205Phe)	NKTR, ZBTB47-AS1 (S205F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2337392	NM_005385.4(NKTR):c.3905C>T (p.Thr1302Met)	NKTR, ZBTB47-AS1 (T934M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299622	NM_005385.4(NKTR):c.4294C>T (p.Arg1432Trp)	NKTR, ZBTB47-AS1 (R1180W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2298129	NM_005385.4(NKTR):c.1187G>T (p.Arg396Leu)	NKTR, ZBTB47-AS1 (R143L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2288231	NM_005385.4(NKTR):c.1066G>C (p.Asp356His)	NKTR, ZBTB47-AS1 (D103H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2276619	NM_005385.4(NKTR):c.3719C>T (p.Ala1240Val)	NKTR, ZBTB47-AS1 (A872V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276618	NM_005385.4(NKTR):c.3718G>T (p.Ala1240Ser)	NKTR, ZBTB47-AS1 (A1240S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265027	NM_005385.4(NKTR):c.2522A>G (p.Asn841Ser)	LOC129936565, NKTR +1 more (N588S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260119	NM_005385.4(NKTR):c.4295G>A (p.Arg1432Gln)	NKTR, ZBTB47-AS1 (R1180Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258087	NM_005385.4(NKTR):c.3436T>G (p.Ser1146Ala)	NKTR, ZBTB47-AS1 (S893A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257697	NM_005385.4(NKTR):c.2423C>A (p.Ser808Tyr)	LOC129936565, NKTR +1 more (S555Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255447	NM_005385.4(NKTR):c.3757A>C (p.Thr1253Pro)	NKTR, ZBTB47-AS1 (T885P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248032	NM_005385.4(NKTR):c.1288C>T (p.Arg430Cys)	NKTR, ZBTB47-AS1 (R177C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2237339	NM_005385.4(NKTR):c.3665T>C (p.Ile1222Thr)	NKTR, ZBTB47-AS1 (I1222T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235265	NM_005385.4(NKTR):c.2861G>A (p.Arg954His)	LOC129936566, NKTR +1 more (R701H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225983	NM_005385.4(NKTR):c.3625G>A (p.Gly1209Arg)	NKTR, ZBTB47-AS1 (G841R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215100	NM_005385.4(NKTR):c.1376T>G (p.Ile459Ser)	NKTR, ZBTB47-AS1 (I91S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206544	NM_005385.4(NKTR):c.1735C>T (p.Pro579Ser)	NKTR, ZBTB47-AS1 (P211S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1331682	NM_005385.4(NKTR):c.3919G>A (p.Asp1307Asn)	NKTR, ZBTB47-AS1 (D1054N +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 770519	NM_005385.4(NKTR):c.812T>G (p.Val271Gly)	NKTR, ZBTB47-AS1 (V18G +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign

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Links from Gene

Items: 76