Tpbg Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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85 records found for search term Tpbg

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
407521329	CV3492338	single nucleotide variant	NM_001376922.1(TPBG):c.8G>T (p.Gly3Val)	not specified [RCV004677269]	uncertain significance	6	82364969	82364969	Human		name
329392186	CV2470456	single nucleotide variant	NM_001376922.1(TPBG):c.97T>C (p.Ser33Pro)	not specified [RCV004273481]	uncertain significance	6	82365058	82365058	Human		name
156375754	CV2210300	single nucleotide variant	NM_001376922.1(TPBG):c.283A>G (p.Asn95Asp)	not specified [RCV004089462]	uncertain significance	6	82365244	82365244	Human		name
156335234	CV2333498	single nucleotide variant	NM_001376922.1(TPBG):c.107C>T (p.Ser36Phe)	not specified [RCV004190193]	uncertain significance	6	82365068	82365068	Human		name
155982874	CV2347835	single nucleotide variant	NM_001376922.1(TPBG):c.112G>A (p.Ala38Thr)	not specified [RCV004195487]	uncertain significance	6	82365073	82365073	Human		name
156085274	CV2390556	single nucleotide variant	NM_001376922.1(TPBG):c.151G>A (p.Ala51Thr)	not specified [RCV004239088]	uncertain significance	6	82365112	82365112	Human		name
401778467	CV2709158	single nucleotide variant	NM_001376922.1(TPBG):c.128C>A (p.Ser43Tyr)	not specified [RCV004316343]	uncertain significance	6	82365089	82365089	Human		name
401780788	CV2727821	single nucleotide variant	NM_001376922.1(TPBG):c.170C>G (p.Pro57Arg)	not specified [RCV004323843]	uncertain significance	6	82365131	82365131	Human		name
401894078	CV2770271	single nucleotide variant	NM_001376922.1(TPBG):c.121T>G (p.Phe41Val)	not specified [RCV004356151]	uncertain significance	6	82365082	82365082	Human		name
597787566	CV3611223	single nucleotide variant	NM_001376922.1(TPBG):c.182A>G (p.Gln61Arg)	not specified [RCV004875643]	uncertain significance	6	82365143	82365143	Human		name
598200733	CV3928279	single nucleotide variant	NM_001376922.1(TPBG):c.194T>C (p.Leu65Pro)	not specified [RCV005290043]	likely benign	6	82365155	82365155	Human		name
598200743	CV3928281	single nucleotide variant	NM_001376922.1(TPBG):c.254T>C (p.Val85Ala)	not specified [RCV005290045]	uncertain significance	6	82365215	82365215	Human		name
156190501	CV2206047	single nucleotide variant	NM_001376922.1(TPBG):c.497A>G (p.Asn166Ser)	not specified [RCV004078460]	uncertain significance	6	82365458	82365458	Human		name
156240445	CV2286047	single nucleotide variant	NM_001376922.1(TPBG):c.884C>T (p.Pro295Leu)	not specified [RCV004143945]	uncertain significance	6	82365845	82365845	Human		name
156198717	CV2293717	single nucleotide variant	NM_001376922.1(TPBG):c.953A>G (p.Lys318Arg)	not specified [RCV004155004]	uncertain significance	6	82365914	82365914	Human		name
156055553	CV2388686	single nucleotide variant	NM_001376922.1(TPBG):c.638G>T (p.Arg213Leu)	not specified [RCV004239559]	uncertain significance	6	82365599	82365599	Human		name
405759318	CV3343780	single nucleotide variant	NM_001376922.1(TPBG):c.764G>T (p.Arg255Leu)	not specified [RCV004468336]	uncertain significance	6	82365725	82365725	Human		name
405759324	CV3343781	single nucleotide variant	NM_001376922.1(TPBG):c.811A>C (p.Lys271Gln)	not specified [RCV004468337]	uncertain significance	6	82365772	82365772	Human		name
405759329	CV3343782	single nucleotide variant	NM_001376922.1(TPBG):c.986T>A (p.Met329Lys)	not specified [RCV004468338]	uncertain significance	6	82365947	82365947	Human		name
407521325	CV3492337	single nucleotide variant	NM_001376922.1(TPBG):c.671A>C (p.Tyr224Ser)	not specified [RCV004677268]	uncertain significance	6	82365632	82365632	Human		name
407521334	CV3492340	single nucleotide variant	NM_001376922.1(TPBG):c.619C>G (p.Arg207Gly)	not specified [RCV004677271]	likely benign	6	82365580	82365580	Human		name
597787562	CV3611222	single nucleotide variant	NM_001376922.1(TPBG):c.781G>A (p.Glu261Lys)	not specified [RCV004875642]	uncertain significance	6	82365742	82365742	Human		name
597787571	CV3611224	single nucleotide variant	NM_001376922.1(TPBG):c.670T>C (p.Tyr224His)	not specified [RCV004875644]	uncertain significance	6	82365631	82365631	Human		name
597787574	CV3611225	single nucleotide variant	NM_001376922.1(TPBG):c.749C>T (p.Thr250Ile)	not specified [RCV004875645]	uncertain significance	6	82365710	82365710	Human		name
597787578	CV3611226	single nucleotide variant	NM_001376922.1(TPBG):c.724A>G (p.Ser242Gly)	not specified [RCV004875646]	uncertain significance	6	82365685	82365685	Human		name
597787582	CV3611227	single nucleotide variant	NM_001376922.1(TPBG):c.302A>G (p.Asn101Ser)	not specified [RCV004875647]	uncertain significance	6	82365263	82365263	Human		name
598200739	CV3928280	single nucleotide variant	NM_001376922.1(TPBG):c.859A>G (p.Ile287Val)	not specified [RCV005290044]	likely benign	6	82365820	82365820	Human		name
155997609	CV2287051	single nucleotide variant	NM_001376922.1(TPBG):c.1233A>C (p.Leu411Phe)	not specified [RCV004144931]	uncertain significance	6	82366194	82366194	Human		name
156344953	CV2372847	single nucleotide variant	NM_001376922.1(TPBG):c.1228A>G (p.Arg410Gly)	not specified [RCV004222029]	uncertain significance	6	82366189	82366189	Human		name
405759296	CV3343776	single nucleotide variant	NM_001376922.1(TPBG):c.1132C>G (p.Arg378Gly)	not specified [RCV004468332]	uncertain significance	6	82366093	82366093	Human		name
405759301	CV3343777	single nucleotide variant	NM_001376922.1(TPBG):c.1136A>G (p.Lys379Arg)	not specified [RCV004468333]	uncertain significance	6	82366097	82366097	Human		name
405759307	CV3343778	single nucleotide variant	NM_001376922.1(TPBG):c.1205G>T (p.Arg402Ile)	not specified [RCV004468334]	uncertain significance	6	82366166	82366166	Human		name
407521332	CV3492339	single nucleotide variant	NM_001376922.1(TPBG):c.1111C>T (p.Leu371Phe)	not specified [RCV004677270]	uncertain significance	6	82366072	82366072	Human		name
598200727	CV3928278	single nucleotide variant	NM_001376922.1(TPBG):c.1240C>G (p.Leu414Val)	not specified [RCV005290042]	uncertain significance	6	82366201	82366201	Human		name
151663550	CV1334025	deletion	NM_001376922.1(TPBG):c.351_374del (p.Ala118_Leu125del)	not provided [RCV001839199]	uncertain significance	6	82365310	82365333	Human		name
597787589	CV3611230	single nucleotide variant	NM_001195528.2(TPBGL):c.5C>A (p.Ala2Asp)	not specified [RCV004875649]	uncertain significance	11	75241054	75241054	Human		name
156017409	CV2262854	single nucleotide variant	NM_001195528.2(TPBGL):c.23C>G (p.Pro8Arg)	not specified [RCV004125004]	uncertain significance	11	75241072	75241072	Human		name
156089885	CV2344562	single nucleotide variant	NM_001195528.2(TPBGL):c.46G>T (p.Val16Leu)	not specified [RCV004197339]	uncertain significance	11	75241095	75241095	Human		name
597787585	CV3611228	single nucleotide variant	NM_001195528.2(TPBGL):c.28C>T (p.Leu10Phe)	not specified [RCV004875648]	likely benign	11	75241077	75241077	Human		name
156037919	CV2332581	single nucleotide variant	NM_001195528.2(TPBGL):c.247G>C (p.Gly83Arg)	not specified [RCV004196292]	uncertain significance	11	75241296	75241296	Human		name
329400083	CV2440541	single nucleotide variant	NM_001195528.2(TPBGL):c.177C>A (p.Asp59Glu)	not specified [RCV004256456]	uncertain significance	11	75241226	75241226	Human		name
401725779	CV2687256	single nucleotide variant	NM_001195528.2(TPBGL):c.258C>G (p.Asp86Glu)	not specified [RCV004298196]	uncertain significance	11	75241307	75241307	Human		name
401756911	CV2696646	single nucleotide variant	NM_001195528.2(TPBGL):c.248G>C (p.Gly83Ala)	not specified [RCV004312663]	likely benign	11	75241297	75241297	Human		name
401756915	CV2696647	single nucleotide variant	NM_001195528.2(TPBGL):c.259C>G (p.Gln87Glu)	not specified [RCV004312664]	uncertain significance	11	75241308	75241308	Human		name
401756917	CV2696648	single nucleotide variant	NM_001195528.2(TPBGL):c.290G>C (p.Ser97Thr)	not specified [RCV004312665]	likely benign	11	75241339	75241339	Human		name
405759339	CV3343784	single nucleotide variant	NM_001195528.2(TPBGL):c.241G>T (p.Gly81Trp)	not specified [RCV004468340]	uncertain significance	11	75241290	75241290	Human		name
405759349	CV3343786	single nucleotide variant	NM_001195528.2(TPBGL):c.286C>G (p.Leu96Val)	not specified [RCV004468342]	uncertain significance	11	75241335	75241335	Human		name
598254939	CV3928283	single nucleotide variant	NM_001195528.2(TPBGL):c.218T>C (p.Leu73Pro)	not specified [RCV005278519]	uncertain significance	11	75241267	75241267	Human		name
156066389	CV2193336	single nucleotide variant	NM_001195528.2(TPBGL):c.779G>C (p.Arg260Pro)	not specified [RCV004072841]	uncertain significance	11	75241828	75241828	Human		name
156065137	CV2225248	single nucleotide variant	NM_001195528.2(TPBGL):c.799C>T (p.Pro267Ser)	not specified [RCV004098898]	uncertain significance	11	75241848	75241848	Human		name
156033783	CV2236369	single nucleotide variant	NM_001195528.2(TPBGL):c.838G>A (p.Gly280Arg)	not specified [RCV004108051]	uncertain significance	11	75241887	75241887	Human		name
156261169	CV2287474	single nucleotide variant	NM_001195528.2(TPBGL):c.355A>T (p.Ser119Cys)	not specified [RCV004140942]	uncertain significance	11	75241404	75241404	Human		name
156346435	CV2300567	single nucleotide variant	NM_001195528.2(TPBGL):c.821C>A (p.Pro274Gln)	not specified [RCV004155531]	uncertain significance	11	75241870	75241870	Human		name
155977620	CV2338800	single nucleotide variant	NM_001195528.2(TPBGL):c.403G>A (p.Gly135Ser)	not specified [RCV004182358]	uncertain significance	11	75241452	75241452	Human		name
156185759	CV2377876	single nucleotide variant	NM_001195528.2(TPBGL):c.862A>G (p.Ser288Gly)	not specified [RCV004230448]	likely benign	11	75241911	75241911	Human		name
156084884	CV2390459	single nucleotide variant	NM_001195528.2(TPBGL):c.845G>T (p.Arg282Leu)	not specified [RCV004239001]	uncertain significance	11	75241894	75241894	Human		name
155958501	CV2395191	single nucleotide variant	NM_001195528.2(TPBGL):c.424C>T (p.Pro142Ser)	not specified [RCV004236859]	uncertain significance	11	75241473	75241473	Human		name
329369188	CV2424753	single nucleotide variant	NM_001195528.2(TPBGL):c.568G>C (p.Ala190Pro)	not specified [RCV004248646]	uncertain significance	11	75241617	75241617	Human		name
329366657	CV2441786	single nucleotide variant	NM_001195528.2(TPBGL):c.578G>C (p.Arg193Pro)	not specified [RCV004261992]	uncertain significance	11	75241627	75241627	Human		name
329401058	CV2445952	single nucleotide variant	NM_001195528.2(TPBGL):c.384C>A (p.Asn128Lys)	not specified [RCV004270549]	uncertain significance	11	75241433	75241433	Human		name
329394051	CV2450046	single nucleotide variant	NM_001195528.2(TPBGL):c.859G>C (p.Asp287His)	not specified [RCV004269096]	uncertain significance	11	75241908	75241908	Human		name
329378721	CV2459915	single nucleotide variant	NM_001195528.2(TPBGL):c.916G>A (p.Ala306Thr)	not specified [RCV004279406]	uncertain significance	11	75241965	75241965	Human		name
401756919	CV2696649	single nucleotide variant	NM_001195528.2(TPBGL):c.313C>A (p.His105Asn)	not specified [RCV004312666]	likely benign	11	75241362	75241362	Human		name
401764525	CV2721350	single nucleotide variant	NM_001195528.2(TPBGL):c.831C>G (p.Asp277Glu)	not specified [RCV004322104]	uncertain significance	11	75241880	75241880	Human		name
401729028	CV2729974	single nucleotide variant	NM_001195528.2(TPBGL):c.395C>T (p.Ala132Val)	not specified [RCV004332965]	uncertain significance	11	75241444	75241444	Human		name
405759361	CV3343788	single nucleotide variant	NM_001195528.2(TPBGL):c.658C>G (p.Arg220Gly)	not specified [RCV004468344]	uncertain significance	11	75241707	75241707	Human		name
405759367	CV3343789	single nucleotide variant	NM_001195528.2(TPBGL):c.667G>C (p.Gly223Arg)	not specified [RCV004468345]	uncertain significance	11	75241716	75241716	Human		name
405759373	CV3343790	single nucleotide variant	NM_001195528.2(TPBGL):c.674C>G (p.Pro225Arg)	not specified [RCV004468346]	uncertain significance	11	75241723	75241723	Human		name
405759380	CV3343791	single nucleotide variant	NM_001195528.2(TPBGL):c.694G>A (p.Ala232Thr)	not specified [RCV004468347]	uncertain significance	11	75241743	75241743	Human		name
405759388	CV3343792	single nucleotide variant	NM_001195528.2(TPBGL):c.714C>G (p.Cys238Trp)	not specified [RCV004468348]	uncertain significance	11	75241763	75241763	Human		name
407521337	CV3492341	single nucleotide variant	NM_001195528.2(TPBGL):c.466G>C (p.Gly156Arg)	not specified [RCV004677272]	uncertain significance	11	75241515	75241515	Human		name
407521340	CV3492342	single nucleotide variant	NM_001195528.2(TPBGL):c.842C>T (p.Ala281Val)	not specified [RCV004677273]	uncertain significance	11	75241891	75241891	Human		name
407521343	CV3492343	single nucleotide variant	NM_001195528.2(TPBGL):c.496G>C (p.Ala166Pro)	not specified [RCV004677274]	uncertain significance	11	75241545	75241545	Human		name
407521345	CV3492344	single nucleotide variant	NM_001195528.2(TPBGL):c.973G>A (p.Val325Met)	not specified [RCV004677275]	uncertain significance	11	75242022	75242022	Human		name
407521351	CV3492346	single nucleotide variant	NM_001195528.2(TPBGL):c.668G>A (p.Gly223Asp)	not specified [RCV004677277]	uncertain significance	11	75241717	75241717	Human		name
597787593	CV3611231	single nucleotide variant	NM_001195528.2(TPBGL):c.895G>T (p.Ala299Ser)	not specified [RCV004875650]	uncertain significance	11	75241944	75241944	Human		name
597787597	CV3611232	single nucleotide variant	NM_001195528.2(TPBGL):c.494A>C (p.Asp165Ala)	not specified [RCV004875651]	uncertain significance	11	75241543	75241543	Human		name
597787601	CV3611233	single nucleotide variant	NM_001195528.2(TPBGL):c.956G>C (p.Gly319Ala)	not specified [RCV004875652]	uncertain significance	11	75242005	75242005	Human		name
597787605	CV3611234	single nucleotide variant	NM_001195528.2(TPBGL):c.625G>C (p.Gly209Arg)	not specified [RCV004875653]	uncertain significance	11	75241674	75241674	Human		name
598200750	CV3928282	single nucleotide variant	NM_001195528.2(TPBGL):c.752A>G (p.Asn251Ser)	not specified [RCV005290046]	uncertain significance	11	75241801	75241801	Human		name
598200758	CV3928286	single nucleotide variant	NM_001195528.2(TPBGL):c.544A>C (p.Asn182His)	not specified [RCV005290047]	uncertain significance	11	75241593	75241593	Human		name
598254962	CV3928287	single nucleotide variant	NM_001195528.2(TPBGL):c.505G>C (p.Ala169Pro)	not specified [RCV005278522]	uncertain significance	11	75241554	75241554	Human		name
156187781	CV2195804	single nucleotide variant	NM_001195528.2(TPBGL):c.1017C>G (p.Asn339Lys)	not specified [RCV004076150]	uncertain significance	11	75242066	75242066	Human		name
156331160	CV2218121	single nucleotide variant	NM_001195528.2(TPBGL):c.1012C>T (p.Arg338Cys)	not specified [RCV004086549]	uncertain significance	11	75242061	75242061	Human		name
405759333	CV3343783	single nucleotide variant	NM_001195528.2(TPBGL):c.1130C>T (p.Ser377Phe)	not specified [RCV004468339]	uncertain significance	11	75242179	75242179	Human		name

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