Zbtb32 Variant Search Result - Rat Genome Database

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56 records found for search term Zbtb32

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8636767	CV91992	single nucleotide variant	NM_014383.1(ZBTB32):c.102C>T (p.Thr34=)	Malignant melanoma [RCV000072090]	not provided	19	35714728	35714728	Human		name
597693404	CV3627750	single nucleotide variant	NM_014383.3(ZBTB32):c.35A>G (p.Tyr12Cys)	not specified [RCV004884823]	uncertain significance	19	35714661	35714661	Human		name
156248154	CV2276956	single nucleotide variant	NM_014383.3(ZBTB32):c.178T>C (p.Trp60Arg)	not specified [RCV004140289]	uncertain significance	19	35714804	35714804	Human		name
155920214	CV2343310	single nucleotide variant	NM_014383.3(ZBTB32):c.287C>T (p.Ala96Val)	not specified [RCV004194928]	uncertain significance	19	35714913	35714913	Human		name
401885289	CV2768052	single nucleotide variant	NM_014383.3(ZBTB32):c.202C>T (p.Pro68Ser)	not specified [RCV004348291]	uncertain significance	19	35714828	35714828	Human		name
405807875	CV3356855	single nucleotide variant	NM_014383.3(ZBTB32):c.121C>G (p.Pro41Ala)	not specified [RCV004480925]	uncertain significance	19	35714747	35714747	Human		name
405807877	CV3356856	single nucleotide variant	NM_014383.3(ZBTB32):c.257A>C (p.Gln86Pro)	not specified [RCV004480926]	uncertain significance	19	35714883	35714883	Human		name
598243260	CV3930367	single nucleotide variant	NM_014383.3(ZBTB32):c.245G>A (p.Ser82Asn)	not specified [RCV005297259]	uncertain significance	19	35714871	35714871	Human		name
598243265	CV3930368	single nucleotide variant	NM_014383.3(ZBTB32):c.188G>A (p.Gly63Glu)	not specified [RCV005297260]	uncertain significance	19	35714814	35714814	Human		name
598243268	CV3930369	single nucleotide variant	NM_014383.3(ZBTB32):c.117G>T (p.Glu39Asp)	not specified [RCV005297261]	uncertain significance	19	35714743	35714743	Human		name
8628289	CV83433	single nucleotide variant	NM_014383.1(ZBTB32):c.187G>A (p.Gly63Arg)	Malignant melanoma [RCV000063513]	not provided	19	35714813	35714813	Human		name
8636768	CV91993	single nucleotide variant	NM_014383.1(ZBTB32):c.107G>A (p.Gly36Glu)	Malignant melanoma [RCV000072091]	not provided	19	35714733	35714733	Human		name
155968501	CV2244256	single nucleotide variant	NM_014383.3(ZBTB32):c.577G>A (p.Glu193Lys)	not specified [RCV004100253]	uncertain significance	19	35715203	35715203	Human		name
155991126	CV2281044	single nucleotide variant	NM_014383.3(ZBTB32):c.554A>G (p.Gln185Arg)	not specified [RCV004147321]	uncertain significance	19	35715180	35715180	Human		name
156009125	CV2294306	single nucleotide variant	NM_014383.3(ZBTB32):c.418A>G (p.Arg140Gly)	not specified [RCV004151434]	uncertain significance	19	35715044	35715044	Human		name
156042347	CV2310965	single nucleotide variant	NM_014383.3(ZBTB32):c.806C>T (p.Pro269Leu)	not specified [RCV004163998]	uncertain significance	19	35715432	35715432	Human		name
156045898	CV2315562	single nucleotide variant	NM_014383.3(ZBTB32):c.338G>A (p.Arg113Gln)	not specified [RCV004169604]	uncertain significance	19	35714964	35714964	Human		name
156276484	CV2316540	single nucleotide variant	NM_014383.3(ZBTB32):c.872G>A (p.Arg291Gln)	not specified [RCV004170005]	likely benign	19	35715498	35715498	Human		name
156087214	CV2337664	single nucleotide variant	NM_014383.3(ZBTB32):c.400C>A (p.Pro134Thr)	not specified [RCV004183695]	uncertain significance	19	35715026	35715026	Human		name
329399467	CV2436176	single nucleotide variant	NM_014383.3(ZBTB32):c.631G>T (p.Val211Leu)	not specified [RCV004249809]	uncertain significance	19	35715257	35715257	Human		name
401733730	CV2682624	single nucleotide variant	NM_014383.3(ZBTB32):c.601G>A (p.Gly201Ser)	not specified [RCV004292673]	uncertain significance	19	35715227	35715227	Human		name
401736547	CV2703176	single nucleotide variant	NM_014383.3(ZBTB32):c.718C>A (p.Gln240Lys)	not specified [RCV004315244]	uncertain significance	19	35715344	35715344	Human		name
401771253	CV2722767	single nucleotide variant	NM_014383.3(ZBTB32):c.459G>T (p.Gln153His)	not specified [RCV004325195]	uncertain significance	19	35715085	35715085	Human		name
405807879	CV3356857	single nucleotide variant	NM_014383.3(ZBTB32):c.326G>A (p.Cys109Tyr)	not specified [RCV004480927]	uncertain significance	19	35714952	35714952	Human		name
405807880	CV3356858	single nucleotide variant	NM_014383.3(ZBTB32):c.337C>G (p.Arg113Gly)	not specified [RCV004480928]	uncertain significance	19	35714963	35714963	Human		name
405807885	CV3356860	single nucleotide variant	NM_014383.3(ZBTB32):c.431A>T (p.Asp144Val)	not specified [RCV004480930]	uncertain significance	19	35715057	35715057	Human		name
405807886	CV3356861	single nucleotide variant	NM_014383.3(ZBTB32):c.492G>A (p.Met164Ile)	not specified [RCV004480931]	uncertain significance	19	35715118	35715118	Human		name
405807891	CV3356863	single nucleotide variant	NM_014383.3(ZBTB32):c.769G>A (p.Gly257Arg)	not specified [RCV004480933]	uncertain significance	19	35715395	35715395	Human		name
405807892	CV3356864	single nucleotide variant	NM_014383.3(ZBTB32):c.970G>C (p.Gly324Arg)	not specified [RCV004480934]	uncertain significance	19	35715953	35715953	Human		name
407465957	CV3494049	single nucleotide variant	NM_014383.3(ZBTB32):c.497A>G (p.His166Arg)	not specified [RCV004688907]	uncertain significance	19	35715123	35715123	Human		name
597752653	CV3627745	single nucleotide variant	NM_014383.3(ZBTB32):c.832C>G (p.His278Asp)	not specified [RCV004893015]	uncertain significance	19	35715458	35715458	Human		name
597693436	CV3627746	single nucleotide variant	NM_014383.3(ZBTB32):c.913C>T (p.Leu305Phe)	not specified [RCV004884820]	uncertain significance	19	35715788	35715788	Human		name
597693426	CV3627748	single nucleotide variant	NM_014383.3(ZBTB32):c.542C>T (p.Thr181Met)	not specified [RCV004884821]	uncertain significance	19	35715168	35715168	Human		name
597693414	CV3627749	single nucleotide variant	NM_014383.3(ZBTB32):c.760T>C (p.Trp254Arg)	not specified [RCV004884822]	uncertain significance	19	35715386	35715386	Human		name
597693394	CV3627751	single nucleotide variant	NM_014383.3(ZBTB32):c.799C>A (p.Leu267Met)	not specified [RCV004884824]	uncertain significance	19	35715425	35715425	Human		name
598243256	CV3930366	single nucleotide variant	NM_014383.3(ZBTB32):c.854C>G (p.Ala285Gly)	not specified [RCV005297258]	uncertain significance	19	35715480	35715480	Human		name
598196597	CV3930370	single nucleotide variant	NM_014383.3(ZBTB32):c.829T>C (p.Tyr277His)	not specified [RCV005313542]	uncertain significance	19	35715455	35715455	Human		name
598196611	CV3930372	single nucleotide variant	NM_014383.3(ZBTB32):c.647G>A (p.Arg216Lys)	not specified [RCV005313544]	uncertain significance	19	35715273	35715273	Human		name
598196618	CV3930373	single nucleotide variant	NM_014383.3(ZBTB32):c.929A>G (p.Gln310Arg)	not specified [RCV005313545]	uncertain significance	19	35715804	35715804	Human		name
155913197	CV2245774	single nucleotide variant	NM_014383.3(ZBTB32):c.1109C>G (p.Ser370Cys)	not specified [RCV004111635]	uncertain significance	19	35716217	35716217	Human		name
156143338	CV2358570	single nucleotide variant	NM_014383.3(ZBTB32):c.1304C>T (p.Ala435Val)	not specified [RCV004207451]	uncertain significance	19	35716592	35716592	Human		name
155937903	CV2364935	single nucleotide variant	NM_014383.3(ZBTB32):c.1300G>C (p.Gly434Arg)	not specified [RCV004222231]	likely benign	19	35716588	35716588	Human		name
155991025	CV2372122	single nucleotide variant	NM_014383.3(ZBTB32):c.1280C>G (p.Pro427Arg)	not specified [RCV004221779]	uncertain significance	19	35716568	35716568	Human		name
155993748	CV2379454	single nucleotide variant	NM_014383.3(ZBTB32):c.1121C>A (p.Ala374Glu)	not specified [RCV004223902]	uncertain significance	19	35716229	35716229	Human		name
155935932	CV2379734	single nucleotide variant	NM_014383.3(ZBTB32):c.1082A>C (p.His361Pro)	not specified [RCV004219854]	uncertain significance	19	35716190	35716190	Human		name
329388233	CV2468800	single nucleotide variant	NM_014383.3(ZBTB32):c.1219C>T (p.Pro407Ser)	not specified [RCV004280116]	uncertain significance	19	35716507	35716507	Human		name
401735581	CV2702813	single nucleotide variant	NM_014383.3(ZBTB32):c.1079C>T (p.Pro360Leu)	not specified [RCV004319374]	uncertain significance	19	35716187	35716187	Human		name
401764176	CV2725465	single nucleotide variant	NM_014383.3(ZBTB32):c.1079C>G (p.Pro360Arg)	not specified [RCV004320097]	uncertain significance	19	35716187	35716187	Human		name
401874633	CV2759295	single nucleotide variant	NM_014383.3(ZBTB32):c.1459A>C (p.Thr487Pro)	not specified [RCV004335884]	uncertain significance	19	35716747	35716747	Human		name
401858674	CV2770595	single nucleotide variant	NM_014383.3(ZBTB32):c.1048C>T (p.His350Tyr)	not specified [RCV004349653]	uncertain significance	19	35716156	35716156	Human		name
405807871	CV3356853	single nucleotide variant	NM_014383.3(ZBTB32):c.1027G>A (p.Ala343Thr)	not specified [RCV004480923]	uncertain significance	19	35716135	35716135	Human		name
405807873	CV3356854	single nucleotide variant	NM_014383.3(ZBTB32):c.1097C>A (p.Pro366His)	not specified [RCV004480924]	uncertain significance	19	35716205	35716205	Human		name
407465949	CV3494047	single nucleotide variant	NM_014383.3(ZBTB32):c.1384C>T (p.Arg462Cys)	not specified [RCV004688905]	uncertain significance	19	35716672	35716672	Human		name
598196604	CV3930371	single nucleotide variant	NM_014383.3(ZBTB32):c.1091C>A (p.Pro364Gln)	not specified [RCV005313543]	uncertain significance	19	35716199	35716199	Human		name
8636769	CV91994	single nucleotide variant	NM_014383.1(ZBTB32):c.1312C>T (p.Pro438Ser)	Malignant melanoma [RCV000072092]	not provided	19	35716600	35716600	Human		name
8636770	CV91995	single nucleotide variant	NM_014383.1(ZBTB32):c.1313C>T (p.Pro438Leu)	Malignant melanoma [RCV000072093]	not provided	19	35716601	35716601	Human		name

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