Tcerg1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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149 records found for search term Tcerg1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401917982	CV2825371	single nucleotide variant	NM_001382548.1(TCERG1):c.96G>A (p.Pro32=)	not provided [RCV003429865]	likely benign	5	146455092	146455092	Human		name
156276754	CV2230593	single nucleotide variant	NM_001382548.1(TCERG1):c.10C>G (p.Arg4Gly)	not specified [RCV004097555]	uncertain significance	5	146447359	146447359	Human		name
401783904	CV2724362	single nucleotide variant	NM_001382548.1(TCERG1):c.22G>T (p.Gly8Trp)	not specified [RCV004328225]	uncertain significance	5	146447371	146447371	Human		name
597772035	CV3615675	single nucleotide variant	NM_001382548.1(TCERG1):c.286A>C (p.Arg96=)	not specified [RCV004871773]	likely benign	5	146457183	146457183	Human		name
597772063	CV3615680	single nucleotide variant	NM_001382548.1(TCERG1):c.23G>C (p.Gly8Ala)	not specified [RCV004871778]	uncertain significance	5	146447372	146447372	Human		name
401915227	CV2825372	single nucleotide variant	NM_001382548.1(TCERG1):c.621T>C (p.Ala207=)	not provided [RCV003428660]	likely benign	5	146459066	146459066	Human		name
401915232	CV2825373	single nucleotide variant	NM_001382548.1(TCERG1):c.621T>G (p.Ala207=)	not provided [RCV003428661]	likely benign	5	146459066	146459066	Human		name
401915235	CV2825374	single nucleotide variant	NM_001382548.1(TCERG1):c.630G>A (p.Gln210=)	not provided [RCV003428662]	likely benign	5	146459075	146459075	Human		name
401917984	CV2825375	single nucleotide variant	NM_001382548.1(TCERG1):c.636G>A (p.Gln212=)	not provided [RCV003429866]	likely benign	5	146459081	146459081	Human		name
401917985	CV2825376	single nucleotide variant	NM_001382548.1(TCERG1):c.639C>A (p.Ala213=)	not provided [RCV003429867]	likely benign	5	146459084	146459084	Human		name
401917987	CV2825377	single nucleotide variant	NM_001382548.1(TCERG1):c.642G>A (p.Gln214=)	not provided [RCV003429868]	likely benign	5	146459087	146459087	Human		name
407512855	CV3485828	single nucleotide variant	NM_001382548.1(TCERG1):c.95C>T (p.Pro32Leu)	not specified [RCV004673611]	uncertain significance	5	146455091	146455091	Human		name
597772078	CV3615683	single nucleotide variant	NM_001382548.1(TCERG1):c.47C>G (p.Pro16Arg)	not specified [RCV004871781]	uncertain significance	5	146447396	146447396	Human		name
616939450	CV4013941	single nucleotide variant	NM_001382548.1(TCERG1):c.633C>T (p.Ala211=)	not provided [RCV005413433]	likely benign	5	146459078	146459078	Human		name
126729569	CV985860	deletion	NM_001382548.1(TCERG1):c.192del (p.Pro65fs)	Colorectal cancer [RCV001293848]	pathogenic	5	146455187	146455187	Human	2	name
401917988	CV2825378	single nucleotide variant	NM_001382548.1(TCERG1):c.2877A>G (p.Lys959=)	not provided [RCV003429869]	likely benign	5	146507123	146507123	Human		name
597772030	CV3615674	single nucleotide variant	NM_001382548.1(TCERG1):c.248G>T (p.Gly83Val)	not specified [RCV004871772]	uncertain significance	5	146455244	146455244	Human		name
597772052	CV3615678	single nucleotide variant	NM_001382548.1(TCERG1):c.275C>T (p.Pro92Leu)	not specified [RCV004871776]	uncertain significance	5	146455271	146455271	Human		name
15112484	CV749323	single nucleotide variant	NM_001382548.1(TCERG1):c.2217A>G (p.Lys739=)	not provided [RCV000916919]	likely benign	5	146492973	146492973	Human		name
8625949	CV81093	single nucleotide variant	NM_001040006.1(TCERG1):c.2241C>T (p.Asp747=)	Malignant melanoma [RCV000061171]	not provided	5	146498608	146498608	Human		name
156268946	CV2195053	single nucleotide variant	NM_001382548.1(TCERG1):c.821C>A (p.Thr274Lys)	not specified [RCV004077970]	uncertain significance	5	146459266	146459266	Human		name
156380607	CV2208291	single nucleotide variant	NM_001382548.1(TCERG1):c.457C>T (p.Arg153Trp)	not specified [RCV004088731]	uncertain significance	5	146458902	146458902	Human		name
156267980	CV2244140	single nucleotide variant	NM_001382548.1(TCERG1):c.479C>T (p.Thr160Ile)	not specified [RCV004108596]	uncertain significance	5	146458924	146458924	Human		name
155922250	CV2284307	single nucleotide variant	NM_001382548.1(TCERG1):c.986T>C (p.Val329Ala)	not specified [RCV004146659]	uncertain significance	5	146463644	146463644	Human		name
156003285	CV2293451	single nucleotide variant	NM_001382548.1(TCERG1):c.989A>C (p.Gln330Pro)	not specified [RCV004152695]	uncertain significance	5	146463647	146463647	Human		name
156003299	CV2293452	single nucleotide variant	NM_001382548.1(TCERG1):c.990A>C (p.Gln330His)	not specified [RCV004152696]	uncertain significance	5	146463648	146463648	Human		name
156053846	CV2344590	single nucleotide variant	NM_001382548.1(TCERG1):c.614C>T (p.Ala205Val)	not specified [RCV004197363]	uncertain significance	5	146459059	146459059	Human		name
401733763	CV2687827	single nucleotide variant	NM_001382548.1(TCERG1):c.911A>G (p.Gln304Arg)	not specified [RCV004303137]	uncertain significance	5	146463569	146463569	Human		name
405746721	CV3331773	single nucleotide variant	NM_001382548.1(TCERG1):c.584C>T (p.Ala195Val)	not specified [RCV004466404]	uncertain significance	5	146459029	146459029	Human		name
405746711	CV3331774	single nucleotide variant	NM_001382548.1(TCERG1):c.734C>T (p.Ala245Val)	not specified [RCV004466405]	uncertain significance	5	146459179	146459179	Human		name
405746701	CV3331775	single nucleotide variant	NM_001382548.1(TCERG1):c.758C>T (p.Ala253Val)	not specified [RCV004466406]	uncertain significance	5	146459203	146459203	Human		name
407512852	CV3485827	single nucleotide variant	NM_001382548.1(TCERG1):c.592C>G (p.Gln198Glu)	not specified [RCV004673610]	uncertain significance	5	146459037	146459037	Human		name
407530755	CV3485829	single nucleotide variant	NM_001382548.1(TCERG1):c.443A>G (p.Tyr148Cys)	not specified [RCV004682072]	uncertain significance	5	146458888	146458888	Human		name
597772047	CV3615677	single nucleotide variant	NM_001382548.1(TCERG1):c.700C>G (p.Gln234Glu)	not specified [RCV004871775]	uncertain significance	5	146459145	146459145	Human		name
597772083	CV3615684	single nucleotide variant	NM_001382548.1(TCERG1):c.571G>T (p.Ala191Ser)	not specified [RCV004871782]	uncertain significance	5	146459016	146459016	Human		name
597772089	CV3615685	single nucleotide variant	NM_001382548.1(TCERG1):c.974C>A (p.Thr325Lys)	not specified [RCV004871783]	uncertain significance	5	146463632	146463632	Human		name
598209260	CV3913189	single nucleotide variant	NM_001382548.1(TCERG1):c.740T>C (p.Val247Ala)	not specified [RCV005291661]	likely benign	5	146459185	146459185	Human		name
598209266	CV3913190	single nucleotide variant	NM_001382548.1(TCERG1):c.334G>C (p.Gly112Arg)	not specified [RCV005291662]	uncertain significance	5	146457231	146457231	Human		name
15184967	CV721284	single nucleotide variant	NM_001382548.1(TCERG1):c.836C>T (p.Pro279Leu)	not provided [RCV000886569]	benign	5	146459281	146459281	Human		name
156222665	CV2209030	single nucleotide variant	NM_001382548.1(TCERG1):c.1043T>C (p.Val348Ala)	not specified [RCV004093276]	uncertain significance	5	146463701	146463701	Human		name
156292810	CV2296864	single nucleotide variant	NM_001382548.1(TCERG1):c.1478A>G (p.Asp493Gly)	not specified [RCV004148743]	uncertain significance	5	146470714	146470714	Human		name
155908674	CV2354717	single nucleotide variant	NM_001382548.1(TCERG1):c.2762A>G (p.Lys921Arg)	not specified [RCV004202669]	uncertain significance	5	146503987	146503987	Human		name
156171178	CV2354943	single nucleotide variant	NM_001382548.1(TCERG1):c.2393G>A (p.Arg798Lys)	not specified [RCV004191436]	uncertain significance	5	146498646	146498646	Human		name
156107561	CV2355337	single nucleotide variant	NM_001382548.1(TCERG1):c.1039T>C (p.Ser347Pro)	not specified [RCV004203185]	uncertain significance	5	146463697	146463697	Human		name
156261971	CV2376869	single nucleotide variant	NM_001382548.1(TCERG1):c.1814G>A (p.Ser605Asn)	not specified [RCV004229569]	uncertain significance	5	146479906	146479906	Human		name
156259956	CV2381062	single nucleotide variant	NM_001382548.1(TCERG1):c.2518A>G (p.Ser840Gly)	not specified [RCV004225098]	uncertain significance	5	146503459	146503459	Human		name
156209675	CV2382661	single nucleotide variant	NM_001382548.1(TCERG1):c.1234A>G (p.Met412Val)	not specified [RCV004232978]	uncertain significance	5	146469579	146469579	Human		name
155929330	CV2389131	single nucleotide variant	NM_001382548.1(TCERG1):c.2957C>G (p.Ser986Cys)	not specified [RCV004235462]	uncertain significance	5	146507203	146507203	Human		name
329400475	CV2438375	single nucleotide variant	NM_001382548.1(TCERG1):c.2543A>G (p.Asp848Gly)	not specified [RCV004259533]	uncertain significance	5	146503484	146503484	Human		name
329356925	CV2460616	single nucleotide variant	NM_001382548.1(TCERG1):c.1987G>A (p.Ala663Thr)	not specified [RCV004268884]	uncertain significance	5	146482641	146482641	Human		name
329377586	CV2462683	single nucleotide variant	NM_001382548.1(TCERG1):c.2721G>C (p.Glu907Asp)	not specified [RCV004278617]	uncertain significance	5	146503946	146503946	Human		name
329362882	CV2464817	single nucleotide variant	NM_001382548.1(TCERG1):c.2396A>G (p.Lys799Arg)	not specified [RCV004284766]	uncertain significance	5	146498649	146498649	Human		name
329398513	CV2471133	single nucleotide variant	NM_001382548.1(TCERG1):c.1722G>T (p.Glu574Asp)	not specified [RCV004278386]	uncertain significance	5	146478613	146478613	Human		name
401745341	CV2698518	single nucleotide variant	NM_001382548.1(TCERG1):c.2414C>T (p.Ser805Leu)	not specified [RCV004299015]	uncertain significance	5	146498667	146498667	Human		name
401886050	CV2771042	single nucleotide variant	NM_001382548.1(TCERG1):c.1273A>G (p.Thr425Ala)	not specified [RCV004346054]	uncertain significance	5	146469618	146469618	Human		name
401898717	CV2782623	single nucleotide variant	NM_001382548.1(TCERG1):c.1709A>G (p.Lys570Arg)	not specified [RCV004359647]	uncertain significance	5	146478600	146478600	Human		name
405746069	CV3331767	single nucleotide variant	NM_001382548.1(TCERG1):c.1499A>G (p.Lys500Arg)	not specified [RCV004466398]	uncertain significance	5	146470735	146470735	Human		name
405746075	CV3331768	single nucleotide variant	NM_001382548.1(TCERG1):c.1622A>T (p.Asp541Val)	not specified [RCV004466399]	uncertain significance	5	146478513	146478513	Human		name
405746083	CV3331769	single nucleotide variant	NM_001382548.1(TCERG1):c.1882C>T (p.Arg628Trp)	not specified [RCV004466400]	uncertain significance	5	146480090	146480090	Human		name
405746734	CV3331771	single nucleotide variant	NM_001382548.1(TCERG1):c.2164G>A (p.Val722Met)	not specified [RCV004466402]	uncertain significance	5	146492920	146492920	Human		name
405746728	CV3331772	single nucleotide variant	NM_001382548.1(TCERG1):c.2229G>T (p.Met743Ile)	not specified [RCV004466403]	uncertain significance	5	146492985	146492985	Human		name
407512859	CV3485830	single nucleotide variant	NM_001382548.1(TCERG1):c.1270G>T (p.Ala424Ser)	not specified [RCV004673612]	uncertain significance	5	146469615	146469615	Human		name
597772040	CV3615676	single nucleotide variant	NM_001382548.1(TCERG1):c.1090C>A (p.Pro364Thr)	not specified [RCV004871774]	uncertain significance	5	146463748	146463748	Human		name
597772057	CV3615679	single nucleotide variant	NM_001382548.1(TCERG1):c.2207G>A (p.Arg736Lys)	not specified [RCV004871777]	uncertain significance	5	146492963	146492963	Human		name
597772068	CV3615681	single nucleotide variant	NM_001382548.1(TCERG1):c.1004C>T (p.Pro335Leu)	not specified [RCV004871779]	uncertain significance	5	146463662	146463662	Human		name
597772099	CV3615687	single nucleotide variant	NM_001382548.1(TCERG1):c.2339T>C (p.Ile780Thr)	not specified [RCV004871785]	uncertain significance	5	146498592	146498592	Human		name
598209231	CV3913182	single nucleotide variant	NM_001382548.1(TCERG1):c.1228G>A (p.Val410Ile)	not specified [RCV005291656]	uncertain significance	5	146469573	146469573	Human		name
598209236	CV3913183	single nucleotide variant	NM_001382548.1(TCERG1):c.2233G>A (p.Ala745Thr)	not specified [RCV005291657]	uncertain significance	5	146492989	146492989	Human		name
598209242	CV3913184	single nucleotide variant	NM_001382548.1(TCERG1):c.2633G>A (p.Arg878Lys)	not specified [RCV005291658]	uncertain significance	5	146503858	146503858	Human		name
598209255	CV3913188	single nucleotide variant	NM_001382548.1(TCERG1):c.2948A>G (p.Asp983Gly)	not specified [RCV005291660]	uncertain significance	5	146507194	146507194	Human		name
598163491	CV3913191	single nucleotide variant	NM_001382548.1(TCERG1):c.1396A>G (p.Lys466Glu)	not specified [RCV005283131]	uncertain significance	5	146469741	146469741	Human		name
598209271	CV3913192	single nucleotide variant	NM_001382548.1(TCERG1):c.1720G>A (p.Glu574Lys)	not specified [RCV005291663]	uncertain significance	5	146478611	146478611	Human		name
8631464	CV86668	single nucleotide variant	NM_001040006.1(TCERG1):c.1310A>G (p.Glu437Gly)	Malignant melanoma [RCV000066759]	not provided	5	146469718	146469718	Human		name
8631465	CV86669	single nucleotide variant	NM_001040006.1(TCERG1):c.1325T>C (p.Leu442Pro)	Malignant melanoma [RCV000066760]	not provided	5	146469733	146469733	Human		name
156259337	CV2277819	single nucleotide variant	NM_001382548.1(TCERG1):c.3242C>G (p.Pro1081Arg)	not specified [RCV004147240]	uncertain significance	5	146510536	146510536	Human		name
597772094	CV3615686	single nucleotide variant	NM_001382548.1(TCERG1):c.3056G>A (p.Arg1019Lys)	not specified [RCV004871784]	uncertain significance	5	146509155	146509155	Human		name
598163479	CV3913185	single nucleotide variant	NM_001382548.1(TCERG1):c.3253C>T (p.Arg1085Cys)	not specified [RCV005283129]	uncertain significance	5	146510547	146510547	Human		name
15144560	CV759876	single nucleotide variant	NM_174937.4(TCERG1L):c.856+9G>A	not provided [RCV000922388]	likely benign	10	131260250	131260250	Human		name
8651780	CV128355	single nucleotide variant	NM_174937.3(TCERG1L):c.946-1004C>A	Lung cancer [RCV000108842]	uncertain significance	10	131164214	131164214	Human		name
8651782	CV128357	single nucleotide variant	NM_174937.3(TCERG1L):c.671-2255G>A	Lung cancer [RCV000108844]	uncertain significance	10	131262699	131262699	Human		name
8651781	CV128356	single nucleotide variant	NM_174937.3(TCERG1L):c.856+14020C>T	Lung cancer [RCV000108843]	uncertain significance	10	131246239	131246239	Human		name
329368395	CV2428004	single nucleotide variant	NM_174937.4(TCERG1L):c.81G>C (p.Trp27Cys)	not specified [RCV004254384]	uncertain significance	10	131311555	131311555	Human		name
329377427	CV2462622	single nucleotide variant	NM_174937.4(TCERG1L):c.37C>A (p.Gln13Lys)	not specified [RCV004278566]	uncertain significance	10	131311599	131311599	Human		name
597772143	CV3615695	single nucleotide variant	NM_174937.4(TCERG1L):c.44A>C (p.Gln15Pro)	not specified [RCV004871793]	uncertain significance	10	131311592	131311592	Human		name
15146569	CV712252	single nucleotide variant	NM_174937.4(TCERG1L):c.729C>T (p.Ala243=)	not provided [RCV000967184]	benign\|likely benign	10	131260386	131260386	Human		name
156337573	CV2343071	single nucleotide variant	NM_174937.4(TCERG1L):c.247C>G (p.Pro83Ala)	not specified [RCV004192668]	uncertain significance	10	131311389	131311389	Human		name
155995732	CV2375107	single nucleotide variant	NM_174937.4(TCERG1L):c.223C>T (p.Pro75Ser)	not specified [RCV004230152]	uncertain significance	10	131311413	131311413	Human		name
156205182	CV2385173	single nucleotide variant	NM_174937.4(TCERG1L):c.199C>G (p.Pro67Ala)	not specified [RCV004228426]	uncertain significance	10	131311437	131311437	Human		name
407512866	CV3485832	single nucleotide variant	NM_174937.4(TCERG1L):c.281C>T (p.Pro94Leu)	not specified [RCV004673614]	uncertain significance	10	131311355	131311355	Human		name
597772132	CV3615693	single nucleotide variant	NM_174937.4(TCERG1L):c.280C>T (p.Pro94Ser)	not specified [RCV004871791]	uncertain significance	10	131311356	131311356	Human		name
597772154	CV3615697	single nucleotide variant	NM_174937.4(TCERG1L):c.178C>A (p.Pro60Thr)	not specified [RCV004871795]	uncertain significance	10	131311458	131311458	Human		name
598209284	CV3913195	single nucleotide variant	NM_174937.4(TCERG1L):c.113C>T (p.Pro38Leu)	not specified [RCV005291665]	uncertain significance	10	131311523	131311523	Human		name
15159002	CV752030	single nucleotide variant	NM_174937.4(TCERG1L):c.1305G>A (p.Glu435=)	not provided [RCV000925191]	likely benign	10	131116889	131116889	Human		name
156147490	CV2196965	single nucleotide variant	NM_174937.4(TCERG1L):c.887G>A (p.Arg296His)	not specified [RCV004071422]	uncertain significance	10	131166855	131166855	Human		name
156240637	CV2231293	single nucleotide variant	NM_174937.4(TCERG1L):c.482A>T (p.Asn161Ile)	not specified [RCV004096402]	uncertain significance	10	131309160	131309160	Human		name
156178644	CV2258256	single nucleotide variant	NM_174937.4(TCERG1L):c.509T>C (p.Phe170Ser)	not specified [RCV004121626]	uncertain significance	10	131308372	131308372	Human		name
156247141	CV2276830	single nucleotide variant	NM_174937.4(TCERG1L):c.803A>C (p.His268Pro)	not specified [RCV004140182]	uncertain significance	10	131260312	131260312	Human		name
156209080	CV2304415	single nucleotide variant	NM_174937.4(TCERG1L):c.528G>T (p.Trp176Cys)	not specified [RCV004164517]	uncertain significance	10	131308353	131308353	Human		name
156276926	CV2328111	single nucleotide variant	NM_174937.4(TCERG1L):c.730G>A (p.Ala244Thr)	not specified [RCV004173222]	uncertain significance	10	131260385	131260385	Human		name
156333303	CV2335967	single nucleotide variant	NM_174937.4(TCERG1L):c.721G>A (p.Ala241Thr)	not specified [RCV004189576]	uncertain significance	10	131260394	131260394	Human		name
155931573	CV2362585	single nucleotide variant	NM_174937.4(TCERG1L):c.323T>C (p.Phe108Ser)	not specified [RCV004215240]	uncertain significance	10	131311313	131311313	Human		name
156083578	CV2369036	single nucleotide variant	NM_174937.4(TCERG1L):c.916A>C (p.Lys306Gln)	not specified [RCV004207971]	uncertain significance	10	131166826	131166826	Human		name
156148510	CV2377333	single nucleotide variant	NM_174937.4(TCERG1L):c.742A>G (p.Met248Val)	not specified [RCV004225514]	uncertain significance	10	131260373	131260373	Human		name
329372779	CV2428647	single nucleotide variant	NM_174937.4(TCERG1L):c.956C>T (p.Pro319Leu)	not specified [RCV004255447]	uncertain significance	10	131163200	131163200	Human		name
329364411	CV2447437	single nucleotide variant	NM_174937.4(TCERG1L):c.766C>T (p.Leu256Phe)	not specified [RCV004262711]	uncertain significance	10	131260349	131260349	Human		name
401772200	CV2687446	single nucleotide variant	NM_174937.4(TCERG1L):c.788G>C (p.Ser263Thr)	not specified [RCV004300691]	uncertain significance	10	131260327	131260327	Human		name
401734385	CV2690572	single nucleotide variant	NM_174937.4(TCERG1L):c.799C>T (p.Arg267Cys)	not specified [RCV004304669]	likely benign	10	131260316	131260316	Human		name
401752099	CV2723117	single nucleotide variant	NM_174937.4(TCERG1L):c.901A>T (p.Met301Leu)	not specified [RCV004329372]	uncertain significance	10	131166841	131166841	Human		name
401752640	CV2723303	single nucleotide variant	NM_174937.4(TCERG1L):c.448A>G (p.Ile150Val)	not specified [RCV004329526]	likely benign	10	131309194	131309194	Human		name
405746655	CV3331780	single nucleotide variant	NM_174937.4(TCERG1L):c.365C>T (p.Pro122Leu)	not specified [RCV004466411]	uncertain significance	10	131309277	131309277	Human		name
405746643	CV3331781	single nucleotide variant	NM_174937.4(TCERG1L):c.775C>T (p.Pro259Ser)	not specified [RCV004466412]	uncertain significance	10	131260340	131260340	Human		name
405746635	CV3331782	single nucleotide variant	NM_174937.4(TCERG1L):c.850G>A (p.Val284Ile)	not specified [RCV004466413]	uncertain significance	10	131260265	131260265	Human		name
405746629	CV3331783	single nucleotide variant	NM_174937.4(TCERG1L):c.895G>C (p.Ala299Pro)	not specified [RCV004466414]	uncertain significance	10	131166847	131166847	Human		name
407512863	CV3485831	single nucleotide variant	NM_174937.4(TCERG1L):c.383C>T (p.Pro128Leu)	not specified [RCV004673613]	uncertain significance	10	131309259	131309259	Human		name
407512869	CV3485833	single nucleotide variant	NM_174937.4(TCERG1L):c.712A>G (p.Ile238Val)	not specified [RCV004673615]	uncertain significance	10	131260403	131260403	Human		name
597772138	CV3615694	single nucleotide variant	NM_174937.4(TCERG1L):c.542A>G (p.Glu181Gly)	not specified [RCV004871792]	uncertain significance	10	131308339	131308339	Human		name
597772148	CV3615696	single nucleotide variant	NM_174937.4(TCERG1L):c.604C>A (p.Leu202Met)	not specified [RCV004871794]	uncertain significance	10	131308277	131308277	Human		name
597772159	CV3615698	single nucleotide variant	NM_174937.4(TCERG1L):c.688C>T (p.Leu230Phe)	not specified [RCV004871796]	uncertain significance	10	131260427	131260427	Human		name
598163499	CV3913194	single nucleotide variant	NM_174937.4(TCERG1L):c.964G>C (p.Gly322Arg)	not specified [RCV005283132]	uncertain significance	10	131163192	131163192	Human		name
598209304	CV3913199	single nucleotide variant	NM_174937.4(TCERG1L):c.446C>G (p.Pro149Arg)	not specified [RCV005291669]	uncertain significance	10	131309196	131309196	Human		name
598163506	CV3913201	single nucleotide variant	NM_174937.4(TCERG1L):c.341A>C (p.Gln114Pro)	not specified [RCV005283133]	uncertain significance	10	131311295	131311295	Human		name
598209314	CV3913202	single nucleotide variant	NM_174937.4(TCERG1L):c.310G>C (p.Ala104Pro)	not specified [RCV005291671]	uncertain significance	10	131311326	131311326	Human		name
15123601	CV712253	single nucleotide variant	NM_174937.4(TCERG1L):c.608C>G (p.Ser203Cys)	not provided [RCV000963273]	likely benign	10	131308273	131308273	Human		name
155968820	CV2213228	single nucleotide variant	NM_174937.4(TCERG1L):c.1322C>T (p.Thr441Met)	not specified [RCV004085451]	uncertain significance	10	131116872	131116872	Human		name
156118072	CV2232021	single nucleotide variant	NM_174937.4(TCERG1L):c.1139A>G (p.Asn380Ser)	not specified [RCV004093075]	uncertain significance	10	131146556	131146556	Human		name
155942545	CV2301225	single nucleotide variant	NM_174937.4(TCERG1L):c.1356G>C (p.Glu452Asp)	not specified [RCV004160129]	uncertain significance	10	131116838	131116838	Human		name
156298586	CV2310637	single nucleotide variant	NM_174937.4(TCERG1L):c.1525T>C (p.Tyr509His)	not specified [RCV004157299]	uncertain significance	10	131098385	131098385	Human		name
155970424	CV2335580	single nucleotide variant	NM_174937.4(TCERG1L):c.1655G>A (p.Arg552Gln)	not specified [RCV004193788]	uncertain significance	10	131093268	131093268	Human		name
156115423	CV2349299	single nucleotide variant	NM_174937.4(TCERG1L):c.1331C>T (p.Pro444Leu)	not specified [RCV004199246]	uncertain significance	10	131116863	131116863	Human		name
156132976	CV2382865	single nucleotide variant	NM_174937.4(TCERG1L):c.1640G>A (p.Arg547Gln)	not specified [RCV004217466]	uncertain significance	10	131093283	131093283	Human		name
329367285	CV2427337	single nucleotide variant	NM_174937.4(TCERG1L):c.1421A>G (p.Lys474Arg)	not specified [RCV004248196]	uncertain significance	10	131104329	131104329	Human		name
401779951	CV2676748	single nucleotide variant	NM_174937.4(TCERG1L):c.1647G>C (p.Gln549His)	not specified [RCV004290922]	uncertain significance	10	131093276	131093276	Human		name
401745206	CV2693206	single nucleotide variant	NM_174937.4(TCERG1L):c.1357C>T (p.Arg453Cys)	not specified [RCV004293134]	uncertain significance	10	131116837	131116837	Human		name
401729363	CV2732989	single nucleotide variant	NM_174937.4(TCERG1L):c.1407T>A (p.Phe469Leu)	not specified [RCV004331165]	uncertain significance	10	131104343	131104343	Human		name
401876417	CV2760766	single nucleotide variant	NM_174937.4(TCERG1L):c.1061G>A (p.Arg354Gln)	not specified [RCV004336410]	uncertain significance	10	131146634	131146634	Human		name
405746692	CV3331776	single nucleotide variant	NM_174937.4(TCERG1L):c.1253G>A (p.Arg418Lys)	not specified [RCV004466407]	uncertain significance	10	131134385	131134385	Human		name
405746683	CV3331777	single nucleotide variant	NM_174937.4(TCERG1L):c.1264G>A (p.Glu422Lys)	not specified [RCV004466408]	uncertain significance	10	131116930	131116930	Human		name
405746673	CV3331778	single nucleotide variant	NM_174937.4(TCERG1L):c.1579C>G (p.Leu527Val)	not specified [RCV004466409]	uncertain significance	10	131098331	131098331	Human		name
405746662	CV3331779	single nucleotide variant	NM_174937.4(TCERG1L):c.1748G>A (p.Arg583Gln)	not specified [RCV004466410]	uncertain significance	10	131093175	131093175	Human		name
597772104	CV3615688	single nucleotide variant	NM_174937.4(TCERG1L):c.1319G>C (p.Arg440Thr)	not specified [RCV004871786]	uncertain significance	10	131116875	131116875	Human		name
597772110	CV3615689	single nucleotide variant	NM_174937.4(TCERG1L):c.1521A>C (p.Glu507Asp)	not specified [RCV004871787]	uncertain significance	10	131098389	131098389	Human		name
597772116	CV3615690	single nucleotide variant	NM_174937.4(TCERG1L):c.1129G>A (p.Gly377Arg)	not specified [RCV004871788]	uncertain significance	10	131146566	131146566	Human		name
597772121	CV3615691	single nucleotide variant	NM_174937.4(TCERG1L):c.1325C>T (p.Pro442Leu)	not specified [RCV004871789]	uncertain significance	10	131116869	131116869	Human		name
598209278	CV3913193	single nucleotide variant	NM_174937.4(TCERG1L):c.1247C>G (p.Thr416Ser)	not specified [RCV005291664]	uncertain significance	10	131134391	131134391	Human		name
598209289	CV3913196	single nucleotide variant	NM_174937.4(TCERG1L):c.1363A>G (p.Thr455Ala)	not specified [RCV005291666]	uncertain significance	10	131116831	131116831	Human		name
598209295	CV3913197	single nucleotide variant	NM_174937.4(TCERG1L):c.1310A>C (p.Lys437Thr)	not specified [RCV005291667]	uncertain significance	10	131116884	131116884	Human		name
598209299	CV3913198	single nucleotide variant	NM_174937.4(TCERG1L):c.1207T>C (p.Ser403Pro)	not specified [RCV005291668]	uncertain significance	10	131134431	131134431	Human		name
598209310	CV3913200	single nucleotide variant	NM_174937.4(TCERG1L):c.1412C>G (p.Thr471Ser)	not specified [RCV005291670]	uncertain significance	10	131104338	131104338	Human		name
15177753	CV701253	single nucleotide variant	NM_174937.4(TCERG1L):c.1721G>A (p.Arg574Gln)	not provided [RCV000951114]	likely benign	10	131093202	131093202	Human		name

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