Ube2t Variant Search Result - Rat Genome Database

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57 records found for search term Ube2t

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
151356390	CV1329154	single nucleotide variant	NM_014176.4(UBE2T):c.-4G>T	not specified [RCV001822743]	uncertain significance	1	202335758	202335758	Human		name
156269097	CV1915180	deletion	NM_014176.4(UBE2T):c.384+6del	not provided [RCV002628028]	uncertain significance	1	202333231	202333231	Human		name
10053554	CV196428	single nucleotide variant	NM_014176.4(UBE2T):c.179+5G>A	Fanconi anemia complementation group T [RCV000180790]	pathogenic\|likely pathogenic\|not provided	1	202334984	202334984	Human	1	name
405121363	CV2957695	single nucleotide variant	NM_014176.4(UBE2T):c.469-9C>T	not provided [RCV003667386]	likely benign	1	202331969	202331969	Human		name
405209261	CV3034190	single nucleotide variant	NM_014176.4(UBE2T):c.110-1G>T	not provided [RCV003708425]	likely pathogenic	1	202335059	202335059	Human		name
405221693	CV3056801	single nucleotide variant	NM_014176.4(UBE2T):c.110-9T>C	not provided [RCV003733409]	likely benign	1	202335067	202335067	Human		name
597908241	CV3738778	single nucleotide variant	NM_014176.4(UBE2T):c.109+1G>A	not provided [RCV005073013]	likely pathogenic	1	202335645	202335645	Human		name
597848177	CV3783137	single nucleotide variant	NM_014176.4(UBE2T):c.180-9C>G	not provided [RCV005123839]	likely benign	1	202333564	202333564	Human		name
150437961	CV1221096	single nucleotide variant	NM_014176.4(UBE2T):c.385-11T>C	Fanconi anemia complementation group T [RCV005232636]\|not provided [RCV001609790]	benign	1	202333104	202333104	Human	1	name
156250059	CV2029567	deletion	NM_014176.4(UBE2T):c.469-20del	not provided [RCV002745957]	benign	1	202331980	202331980	Human		name
155998444	CV2167885	single nucleotide variant	NM_014176.4(UBE2T):c.384+19C>G	not provided [RCV003034656]	likely benign	1	202333218	202333218	Human		name
402498876	CV2926641	deletion	NM_014176.4(UBE2T):c.286-15del	not provided [RCV003573784]	likely benign	1	202333350	202333350	Human		name
405184923	CV3040321	single nucleotide variant	NM_014176.4(UBE2T):c.384+10C>T	not provided [RCV003705923]	likely benign	1	202333227	202333227	Human		name
597865960	CV3794380	single nucleotide variant	NM_014176.4(UBE2T):c.384+20T>C	not provided [RCV005140556]	likely benign	1	202333217	202333217	Human		name
597907730	CV3830060	single nucleotide variant	NM_014176.4(UBE2T):c.285+18G>A	not provided [RCV005182629]	likely benign	1	202333432	202333432	Human		name
150494085	CV1226090	single nucleotide variant	NM_014176.4(UBE2T):c.180-307A>T	not provided [RCV001619308]	benign	1	202333862	202333862	Human		name
150511724	CV1242784	single nucleotide variant	NM_014176.4(UBE2T):c.469-203T>C	not provided [RCV001661137]	benign	1	202332163	202332163	Human		name
150452747	CV1260434	single nucleotide variant	NM_014176.4(UBE2T):c.15A>G (p.Ser5=)	Fanconi anemia complementation group T [RCV002243405]\|not provided [RCV001680924]	benign	1	202335740	202335740	Human	1	name
10053553	CV196427	single nucleotide variant	NM_014176.4(UBE2T):c.4C>G (p.Gln2Glu)	Fanconi anemia complementation group T [RCV000180789]	pathogenic	1	202335751	202335751	Human	1	name
405073041	CV2940519	deletion	NM_014176.4(UBE2T):c.109+18_109+23del	not provided [RCV003659534]	likely benign	1	202335623	202335628	Human		name
405062035	CV3020502	microsatellite	NM_014176.4(UBE2T):c.110-15_110-12del	not provided [RCV003697755]	likely benign	1	202335070	202335073	Human		name
597907979	CV3826137	single nucleotide variant	NM_014176.4(UBE2T):c.90A>G (p.Gln30=)	not provided [RCV005182873]	likely benign	1	202335665	202335665	Human		name
405209163	CV3061947	single nucleotide variant	NM_014176.4(UBE2T):c.213C>G (p.Leu71=)	not provided [RCV003731742]	likely benign	1	202333522	202333522	Human		name
597885793	CV3814709	single nucleotide variant	NM_014176.4(UBE2T):c.147T>A (p.Gly49=)	not provided [RCV005160850]	likely benign	1	202335021	202335021	Human		name
15188839	CV718528	single nucleotide variant	NM_014176.4(UBE2T):c.201G>A (p.Gln67=)	not provided [RCV000887653]	likely benign	1	202333534	202333534	Human		name
151354866	CV1327933	single nucleotide variant	NM_014176.4(UBE2T):c.387C>G (p.Ser129=)	not specified [RCV001819408]	likely benign	1	202333091	202333091	Human		name
156449725	CV1942052	single nucleotide variant	NM_014176.4(UBE2T):c.71G>A (p.Cys24Tyr)	not provided [RCV003121851]\|not specified [RCV004245901]	uncertain significance	1	202335684	202335684	Human		name
155912219	CV2029491	single nucleotide variant	NM_014176.4(UBE2T):c.46A>T (p.Thr16Ser)	not provided [RCV002750225]	uncertain significance	1	202335709	202335709	Human		name
156075923	CV2160340	single nucleotide variant	NM_014176.4(UBE2T):c.546G>A (p.Lys182=)	not provided [RCV003020187]	likely benign	1	202331883	202331883	Human		name
405048436	CV3025313	single nucleotide variant	NM_014176.4(UBE2T):c.363T>C (p.Asp121=)	not provided [RCV003696831]	likely benign	1	202333258	202333258	Human		name
405198457	CV3032822	single nucleotide variant	NM_014176.4(UBE2T):c.312C>T (p.Ile104=)	not provided [RCV003707200]	likely benign	1	202333309	202333309	Human		name
597863419	CV3796904	deletion	NM_014176.4(UBE2T):c.167del (p.Ile56fs)	not provided [RCV005137802]	pathogenic	1	202335001	202335001	Human		name
597860694	CV3800650	single nucleotide variant	NM_014176.4(UBE2T):c.369G>A (p.Pro123=)	not provided [RCV005135050]	likely benign	1	202333252	202333252	Human		name
597897588	CV3827277	single nucleotide variant	NM_014176.4(UBE2T):c.318T>C (p.Thr106=)	not provided [RCV005172548]	likely benign	1	202333303	202333303	Human		name
597907930	CV3830228	single nucleotide variant	NM_014176.4(UBE2T):c.381C>T (p.Asp127=)	not provided [RCV005182798]	likely benign	1	202333240	202333240	Human		name
597908146	CV3833731	single nucleotide variant	NM_014176.4(UBE2T):c.498A>G (p.Leu166=)	not provided [RCV005183091]	likely benign	1	202331931	202331931	Human		name
597918532	CV3841407	deletion	NM_014176.4(UBE2T):c.134del (p.Pro45fs)	not provided [RCV005193510]	pathogenic	1	202335034	202335034	Human		name
34889188	CV917947	deletion	NM_014176.3(UBE2T):c.-65+1253_*12383del	Fanconi anemia complementation group T [RCV001194884]	pathogenic				Human	1	name
34889186	CV917948	deletion	NM_014176.4(UBE2T):c.110-280_468+264del	Fanconi anemia complementation group T [RCV001194882]	pathogenic	1	202332746	202335338	Human	1	name
34889187	CV917949	duplication	NM_014176.4(UBE2T):c.110-280_468+264dup	Fanconi anemia complementation group T [RCV001194883]	pathogenic	1	202332745	202332746	Human	1	name
126744667	CV1015616	single nucleotide variant	NM_014176.4(UBE2T):c.103C>T (p.Arg35Ter)	Fanconi anemia, complementation group T [RCV001330489]	pathogenic	1	202335652	202335652	Human		name
127270796	CV1058531	duplication	NM_014176.4(UBE2T):c.368dup (p.Leu124fs)	not provided [RCV001389953]	pathogenic	1	202333252	202333253	Human		name
156284764	CV1884741	single nucleotide variant	NM_014176.4(UBE2T):c.172C>G (p.Pro58Ala)	not provided [RCV003061200]	uncertain significance	1	202334996	202334996	Human		name
156021647	CV2105754	single nucleotide variant	NM_014176.4(UBE2T):c.106G>A (p.Ala36Thr)	not provided [RCV002923093]	conflicting interpretations of pathogenicity\|uncertain significance	1	202335649	202335649	Human		name
597682712	CV3625864	single nucleotide variant	NM_014176.4(UBE2T):c.286G>C (p.Gly96Arg)	not specified [RCV004883709]	uncertain significance	1	202333335	202333335	Human		name
597879167	CV3816943	single nucleotide variant	NM_014176.4(UBE2T):c.109C>T (p.Gln37Ter)	not provided [RCV005154340]	pathogenic	1	202335646	202335646	Human		name
597900803	CV3823170	single nucleotide variant	NM_014176.4(UBE2T):c.205C>T (p.Arg69Ter)	not provided [RCV005175520]	pathogenic	1	202333530	202333530	Human		name
598189131	CV3932733	single nucleotide variant	NM_014176.4(UBE2T):c.220A>G (p.Ile74Val)	not specified [RCV005288031]	uncertain significance	1	202333515	202333515	Human		name
151355389	CV1328456	single nucleotide variant	NM_014176.4(UBE2T):c.509G>T (p.Gly170Val)	not provided [RCV003772317]\|not specified [RCV001820461]	uncertain significance	1	202331920	202331920	Human		name
155740640	CV1779693	single nucleotide variant	NM_014176.4(UBE2T):c.560T>C (p.Val187Ala)	not provided [RCV002302309]\|not specified [RCV005288756]	uncertain significance	1	202331869	202331869	Human		name
156359570	CV1904253	single nucleotide variant	NM_014176.4(UBE2T):c.383T>C (p.Ile128Thr)	not provided [RCV002581633]	uncertain significance	1	202333238	202333238	Human		name
156375450	CV2190998	single nucleotide variant	NM_014176.4(UBE2T):c.345G>C (p.Met115Ile)	not provided [RCV003050062]	uncertain significance	1	202333276	202333276	Human		name
407522740	CV3491057	single nucleotide variant	NM_014176.4(UBE2T):c.404A>G (p.Asn135Ser)	not specified [RCV004677799]	uncertain significance	1	202333074	202333074	Human		name
597682701	CV3625865	single nucleotide variant	NM_014176.4(UBE2T):c.427G>A (p.Ala143Thr)	not specified [RCV004883710]	uncertain significance	1	202333051	202333051	Human		name
597889193	CV3830278	single nucleotide variant	NM_014176.4(UBE2T):c.508G>A (p.Gly170Ser)	not provided [RCV005164418]	uncertain significance	1	202331921	202331921	Human		name
597928963	CV3853778	single nucleotide variant	NM_014176.4(UBE2T):c.430A>G (p.Arg144Gly)	not provided [RCV005203261]	uncertain significance	1	202333048	202333048	Human		name
597836096	CV3764531	microsatellite	NM_014176.4(UBE2T):c.329_330dup (p.Ile111fs)	not provided [RCV005107331]	uncertain significance	1	202333290	202333291	Human		name

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