Tsga10ip Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for All species
(View Results for all Objects and Ontologies)

68 records found for search term Tsga10ip

Refine Term:

Sort By:

Export

CSV

TAB

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

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message