Tsga10ip Variant Search Result - Rat Genome Database

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68 records found for search term Tsga10ip

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156364963	CV2272028	single nucleotide variant	NM_152762.3(TSGA10IP):c.5G>A (p.Gly2Glu)	not specified [RCV004124830]	uncertain significance	11	65945680	65945680	Human		name
405798188	CV3340720	single nucleotide variant	NM_152762.3(TSGA10IP):c.59T>C (p.Val20Ala)	not specified [RCV004476464]	likely benign	11	65945734	65945734	Human		name
405798267	CV3340724	single nucleotide variant	NM_152762.3(TSGA10IP):c.80G>A (p.Arg27Gln)	not specified [RCV004476468]	uncertain significance	11	65945755	65945755	Human		name
597787811	CV3617912	single nucleotide variant	NM_152762.3(TSGA10IP):c.88G>A (p.Ala30Thr)	not specified [RCV004875704]	uncertain significance	11	65945763	65945763	Human		name
598216212	CV3928667	single nucleotide variant	NM_152762.3(TSGA10IP):c.88G>T (p.Ala30Ser)	not specified [RCV005292852]	uncertain significance	11	65945763	65945763	Human		name
155905117	CV2285850	single nucleotide variant	NM_152762.3(TSGA10IP):c.119T>G (p.Leu40Arg)	not specified [RCV004143793]	uncertain significance	11	65945794	65945794	Human		name
329357960	CV2453828	single nucleotide variant	NM_152762.3(TSGA10IP):c.125C>T (p.Ser42Leu)	not specified [RCV004271231]	uncertain significance	11	65945800	65945800	Human		name
401738983	CV2676414	single nucleotide variant	NM_152762.3(TSGA10IP):c.128C>T (p.Thr43Ile)	not specified [RCV004286435]	uncertain significance	11	65945803	65945803	Human		name
405798146	CV3340705	single nucleotide variant	NM_152762.3(TSGA10IP):c.130G>A (p.Val44Ile)	not specified [RCV004476449]	likely benign	11	65945805	65945805	Human		name
405798157	CV3340709	single nucleotide variant	NM_152762.3(TSGA10IP):c.232C>T (p.Arg78Cys)	not specified [RCV004476453]	uncertain significance	11	65946964	65946964	Human		name
405798160	CV3340710	single nucleotide variant	NM_152762.3(TSGA10IP):c.249G>C (p.Gln83His)	not specified [RCV004476454]	uncertain significance	11	65946981	65946981	Human		name
405798163	CV3340711	single nucleotide variant	NM_152762.3(TSGA10IP):c.269C>A (p.Ser90Tyr)	not specified [RCV004476455]	uncertain significance	11	65947001	65947001	Human		name
407528450	CV3486967	single nucleotide variant	NM_152762.3(TSGA10IP):c.205A>G (p.Ser69Gly)	not specified [RCV004680388]	uncertain significance	11	65946937	65946937	Human		name
155989432	CV2244251	single nucleotide variant	NM_152762.3(TSGA10IP):c.589G>T (p.Gly197Cys)	not specified [RCV004100248]	uncertain significance	11	65947414	65947414	Human		name
156251705	CV2273428	single nucleotide variant	NM_152762.3(TSGA10IP):c.547A>G (p.Ile183Val)	not specified [RCV004132186]	uncertain significance	11	65947372	65947372	Human		name
156169953	CV2276856	single nucleotide variant	NM_152762.3(TSGA10IP):c.626C>T (p.Ser209Leu)	not specified [RCV004140200]	uncertain significance	11	65947451	65947451	Human		name
156174897	CV2278170	single nucleotide variant	NM_152762.3(TSGA10IP):c.508A>C (p.Lys170Gln)	not specified [RCV004141368]	uncertain significance	11	65947333	65947333	Human		name
401776428	CV2689136	single nucleotide variant	NM_152762.3(TSGA10IP):c.431G>A (p.Arg144His)	not specified [RCV004312417]	likely benign	11	65947256	65947256	Human		name
401779041	CV2702064	single nucleotide variant	NM_152762.3(TSGA10IP):c.848C>T (p.Ser283Phe)	not specified [RCV004320641]	uncertain significance	11	65947673	65947673	Human		name
401774380	CV2727823	single nucleotide variant	NM_152762.3(TSGA10IP):c.948G>C (p.Gln316His)	not specified [RCV004323845]	uncertain significance	11	65947773	65947773	Human		name
401861461	CV2759596	single nucleotide variant	NM_152762.3(TSGA10IP):c.442C>A (p.Arg148Ser)	not specified [RCV004338571]	uncertain significance	11	65947267	65947267	Human		name
401890377	CV2768159	single nucleotide variant	NM_152762.3(TSGA10IP):c.343A>T (p.Ile115Phe)	not specified [RCV004350171]	likely benign	11	65947168	65947168	Human		name
401866518	CV2782866	single nucleotide variant	NM_152762.3(TSGA10IP):c.607A>G (p.Arg203Gly)	not specified [RCV004361674]	uncertain significance	11	65947432	65947432	Human		name
405798166	CV3340712	single nucleotide variant	NM_152762.3(TSGA10IP):c.319C>A (p.Pro107Thr)	not specified [RCV004476456]	uncertain significance	11	65947144	65947144	Human		name
405798169	CV3340713	single nucleotide variant	NM_152762.3(TSGA10IP):c.442C>T (p.Arg148Cys)	not specified [RCV004476457]	uncertain significance	11	65947267	65947267	Human		name
405798170	CV3340714	single nucleotide variant	NM_152762.3(TSGA10IP):c.443G>A (p.Arg148His)	not specified [RCV004476458]	uncertain significance	11	65947268	65947268	Human		name
405798173	CV3340715	single nucleotide variant	NM_152762.3(TSGA10IP):c.470C>T (p.Ala157Val)	not specified [RCV004476459]	uncertain significance	11	65947295	65947295	Human		name
405798176	CV3340716	single nucleotide variant	NM_152762.3(TSGA10IP):c.497C>T (p.Ala166Val)	not specified [RCV004476460]	likely benign	11	65947322	65947322	Human		name
405798179	CV3340717	single nucleotide variant	NM_152762.3(TSGA10IP):c.511G>C (p.Ala171Pro)	not specified [RCV004476461]	uncertain significance	11	65947336	65947336	Human		name
405798182	CV3340718	single nucleotide variant	NM_152762.3(TSGA10IP):c.580C>T (p.Pro194Ser)	not specified [RCV004476462]	uncertain significance	11	65947405	65947405	Human		name
405798185	CV3340719	single nucleotide variant	NM_152762.3(TSGA10IP):c.581C>T (p.Pro194Leu)	not specified [RCV004476463]	uncertain significance	11	65947406	65947406	Human		name
405798189	CV3340721	single nucleotide variant	NM_152762.3(TSGA10IP):c.643G>T (p.Val215Phe)	not specified [RCV004476465]	uncertain significance	11	65947468	65947468	Human		name
405798192	CV3340722	single nucleotide variant	NM_152762.3(TSGA10IP):c.657C>G (p.Ser219Arg)	not specified [RCV004476466]	uncertain significance	11	65947482	65947482	Human		name
405798264	CV3340723	single nucleotide variant	NM_152762.3(TSGA10IP):c.676G>A (p.Glu226Lys)	not specified [RCV004476467]	uncertain significance	11	65947501	65947501	Human		name
405798269	CV3340725	single nucleotide variant	NM_152762.3(TSGA10IP):c.822G>T (p.Lys274Asn)	not specified [RCV004476469]	uncertain significance	11	65947647	65947647	Human		name
405798272	CV3340726	single nucleotide variant	NM_152762.3(TSGA10IP):c.857G>A (p.Gly286Glu)	not specified [RCV004476470]	uncertain significance	11	65947682	65947682	Human		name
597787814	CV3617913	single nucleotide variant	NM_152762.3(TSGA10IP):c.473A>G (p.His158Arg)	not specified [RCV004875705]	uncertain significance	11	65947298	65947298	Human		name
597787819	CV3617914	single nucleotide variant	NM_152762.3(TSGA10IP):c.871C>A (p.Gln291Lys)	not specified [RCV004875706]	uncertain significance	11	65947696	65947696	Human		name
598237867	CV3928663	single nucleotide variant	NM_152762.3(TSGA10IP):c.790C>T (p.Pro264Ser)	not specified [RCV005296326]	uncertain significance	11	65947615	65947615	Human		name
156147817	CV2212863	single nucleotide variant	NM_152762.3(TSGA10IP):c.1075G>A (p.Ala359Thr)	not specified [RCV004091521]	uncertain significance	11	65948072	65948072	Human		name
156246208	CV2219056	single nucleotide variant	NM_152762.3(TSGA10IP):c.1058G>A (p.Arg353Gln)	not specified [RCV004087224]	likely benign	11	65948055	65948055	Human		name
156339255	CV2225063	single nucleotide variant	NM_152762.3(TSGA10IP):c.1035G>T (p.Arg345Ser)	not specified [RCV004094885]	uncertain significance	11	65948032	65948032	Human		name
156086025	CV2244661	single nucleotide variant	NM_152762.3(TSGA10IP):c.1273A>G (p.Arg425Gly)	not specified [RCV004102372]	uncertain significance	11	65953688	65953688	Human		name
156396310	CV2326206	single nucleotide variant	NM_152762.3(TSGA10IP):c.1244T>G (p.Val415Gly)	not specified [RCV004180471]	uncertain significance	11	65953659	65953659	Human		name
156232622	CV2346127	single nucleotide variant	NM_152762.3(TSGA10IP):c.1099G>A (p.Val367Met)	not specified [RCV004201590]	uncertain significance	11	65948096	65948096	Human		name
329386551	CV2428295	single nucleotide variant	NM_152762.3(TSGA10IP):c.1120C>T (p.Arg374Cys)	not specified [RCV004251319]	uncertain significance	11	65948117	65948117	Human		name
329351998	CV2455593	single nucleotide variant	NM_152762.3(TSGA10IP):c.1432C>G (p.Arg478Gly)	not specified [RCV004276843]	uncertain significance	11	65959199	65959199	Human		name
401761773	CV2699409	single nucleotide variant	NM_152762.3(TSGA10IP):c.1613C>A (p.Thr538Asn)	not specified [RCV004305985]	uncertain significance	11	65959882	65959882	Human		name
401880566	CV2780244	single nucleotide variant	NM_152762.3(TSGA10IP):c.1135C>G (p.Arg379Gly)	not specified [RCV004355880]	uncertain significance	11	65948132	65948132	Human		name
401872057	CV2792967	single nucleotide variant	NM_152762.3(TSGA10IP):c.1112T>C (p.Leu371Pro)	not specified [RCV004360310]	uncertain significance	11	65948109	65948109	Human		name
405798138	CV3340702	single nucleotide variant	NM_152762.3(TSGA10IP):c.1093A>T (p.Thr365Ser)	not specified [RCV004476446]	uncertain significance	11	65948090	65948090	Human		name
405798141	CV3340703	single nucleotide variant	NM_152762.3(TSGA10IP):c.1121G>A (p.Arg374His)	not specified [RCV004476447]	uncertain significance	11	65948118	65948118	Human		name
405798143	CV3340704	single nucleotide variant	NM_152762.3(TSGA10IP):c.1214G>A (p.Arg405Gln)	not specified [RCV004476448]	uncertain significance	11	65953629	65953629	Human		name
405798148	CV3340706	single nucleotide variant	NM_152762.3(TSGA10IP):c.1340G>A (p.Arg447His)	not specified [RCV004476450]	uncertain significance	11	65958900	65958900	Human		name
405798151	CV3340707	single nucleotide variant	NM_152762.3(TSGA10IP):c.1448G>A (p.Arg483Gln)	not specified [RCV004476451]	uncertain significance	11	65959215	65959215	Human		name
405798154	CV3340708	single nucleotide variant	NM_152762.3(TSGA10IP):c.1651G>C (p.Asp551His)	not specified [RCV004476452]	uncertain significance	11	65959920	65959920	Human		name
407528446	CV3486965	single nucleotide variant	NM_152762.3(TSGA10IP):c.1657G>A (p.Glu553Lys)	not specified [RCV004680386]	uncertain significance	11	65959926	65959926	Human		name
407528452	CV3486968	single nucleotide variant	NM_152762.3(TSGA10IP):c.1576G>C (p.Glu526Gln)	not specified [RCV004680389]	uncertain significance	11	65959845	65959845	Human		name
597787799	CV3617908	single nucleotide variant	NM_152762.3(TSGA10IP):c.1447C>T (p.Arg483Trp)	not specified [RCV004875701]	uncertain significance	11	65959214	65959214	Human		name
597787803	CV3617909	single nucleotide variant	NM_152762.3(TSGA10IP):c.1174C>T (p.Arg392Trp)	not specified [RCV004875702]	uncertain significance	11	65953589	65953589	Human		name
597787806	CV3617911	single nucleotide variant	NM_152762.3(TSGA10IP):c.1433G>A (p.Arg478Gln)	not specified [RCV004875703]	uncertain significance	11	65959200	65959200	Human		name
597787821	CV3617915	single nucleotide variant	NM_152762.3(TSGA10IP):c.1004G>A (p.Gly335Asp)	not specified [RCV004875707]	uncertain significance	11	65948001	65948001	Human		name
598216197	CV3928664	single nucleotide variant	NM_152762.3(TSGA10IP):c.1358C>T (p.Ala453Val)	not specified [RCV005292850]	uncertain significance	11	65958918	65958918	Human		name
598237874	CV3928665	single nucleotide variant	NM_152762.3(TSGA10IP):c.1325G>A (p.Arg442His)	not specified [RCV005296327]	uncertain significance	11	65958885	65958885	Human		name
598216204	CV3928666	single nucleotide variant	NM_152762.3(TSGA10IP):c.1034G>A (p.Arg345Lys)	not specified [RCV005292851]	uncertain significance	11	65948031	65948031	Human		name
598237882	CV3928668	single nucleotide variant	NM_152762.3(TSGA10IP):c.1496T>A (p.Leu499Gln)	not specified [RCV005296328]	uncertain significance	11	65959263	65959263	Human		name
8634295	CV89515	single nucleotide variant	NM_152762.2(TSGA10IP):c.1666C>T (p.Pro556Ser)	Malignant melanoma [RCV000069612]	not provided	11	65959935	65959935	Human		name
8634296	CV89516	single nucleotide variant	NM_152762.2(TSGA10IP):c.1667C>T (p.Pro556Leu)	Malignant melanoma [RCV000069613]	not provided	11	65959936	65959936	Human		name

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