Vat1 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

79 records found for search term Vat1

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597803668	CV3633190	single nucleotide variant	NM_006373.4(VAT1):c.7G>C (p.Asp3His)	not specified [RCV004881854]	uncertain significance	17	43022316	43022316	Human		name
156146300	CV2218910	single nucleotide variant	NM_006373.4(VAT1):c.37G>A (p.Gly13Arg)	not specified [RCV004085135]	uncertain significance	17	43022286	43022286	Human		name
155985264	CV2270670	single nucleotide variant	NM_006373.4(VAT1):c.38G>A (p.Gly13Glu)	not specified [RCV004137881]	uncertain significance	17	43022285	43022285	Human		name
156192063	CV2301857	single nucleotide variant	NM_006373.4(VAT1):c.97G>T (p.Ala33Ser)	not specified [RCV004156649]	uncertain significance	17	43022226	43022226	Human		name
405806405	CV3348838	single nucleotide variant	NM_006373.4(VAT1):c.44A>T (p.Asp15Val)	not specified [RCV004480170]	uncertain significance	17	43022279	43022279	Human		name
329381965	CV2424281	single nucleotide variant	NM_006373.4(VAT1):c.161C>T (p.Thr54Ile)	not specified [RCV004252190]	uncertain significance	17	43022162	43022162	Human		name
405806401	CV3348836	single nucleotide variant	NM_006373.4(VAT1):c.127G>C (p.Ala43Pro)	not specified [RCV004480168]	uncertain significance	17	43022196	43022196	Human		name
405806403	CV3348837	single nucleotide variant	NM_006373.4(VAT1):c.217G>A (p.Ala73Thr)	not specified [RCV004480169]	uncertain significance	17	43022106	43022106	Human		name
407529397	CV3493335	single nucleotide variant	NM_006373.4(VAT1):c.163G>A (p.Gly55Ser)	not specified [RCV004680887]	uncertain significance	17	43022160	43022160	Human		name
15181611	CV740788	single nucleotide variant	NM_006373.4(VAT1):c.115G>A (p.Ala39Thr)	not provided [RCV000907620]	benign	17	43022208	43022208	Human		name
156242771	CV2210763	single nucleotide variant	NM_006373.4(VAT1):c.678C>A (p.His226Gln)	not specified [RCV004085858]	uncertain significance	17	43018124	43018124	Human		name
156330832	CV2224325	single nucleotide variant	NM_006373.4(VAT1):c.628C>T (p.Arg210Cys)	not specified [RCV004096142]	uncertain significance	17	43018174	43018174	Human		name
156365849	CV2272186	single nucleotide variant	NM_006373.4(VAT1):c.847G>A (p.Val283Ile)	not specified [RCV004124956]	uncertain significance	17	43017850	43017850	Human		name
156248848	CV2277041	single nucleotide variant	NM_006373.4(VAT1):c.815G>C (p.Gly272Ala)	not specified [RCV004140361]	uncertain significance	17	43017882	43017882	Human		name
155923124	CV2336785	single nucleotide variant	NM_006373.4(VAT1):c.637G>A (p.Glu213Lys)	not specified [RCV004190408]	uncertain significance	17	43018165	43018165	Human		name
155988995	CV2371883	single nucleotide variant	NM_006373.4(VAT1):c.931G>A (p.Val311Met)	not specified [RCV004221572]	uncertain significance	17	43016474	43016474	Human		name
401757971	CV2685652	single nucleotide variant	NM_006373.4(VAT1):c.961C>T (p.Arg321Trp)	not specified [RCV004294659]	uncertain significance	17	43016444	43016444	Human		name
405806407	CV3348839	single nucleotide variant	NM_006373.4(VAT1):c.959A>G (p.Asn320Ser)	not specified [RCV004480171]	uncertain significance	17	43016446	43016446	Human		name
407529394	CV3493334	single nucleotide variant	NM_006373.4(VAT1):c.398G>A (p.Arg133Gln)	not specified [RCV004680886]	uncertain significance	17	43018789	43018789	Human		name
597803666	CV3633189	single nucleotide variant	NM_006373.4(VAT1):c.854A>G (p.Tyr285Cys)	not specified [RCV004881853]	uncertain significance	17	43017843	43017843	Human		name
597803669	CV3633191	single nucleotide variant	NM_006373.4(VAT1):c.470T>A (p.Ile157Asn)	not specified [RCV004881855]	uncertain significance	17	43018717	43018717	Human		name
598240098	CV3929422	single nucleotide variant	NM_006373.4(VAT1):c.529T>C (p.Tyr177His)	not specified [RCV005296713]	uncertain significance	17	43018658	43018658	Human		name
598240104	CV3929424	single nucleotide variant	NM_006373.4(VAT1):c.812A>G (p.Lys271Arg)	not specified [RCV005296714]	uncertain significance	17	43017885	43017885	Human		name
329358042	CV2427924	single nucleotide variant	NM_006373.4(VAT1):c.1049A>G (p.Asn350Ser)	not specified [RCV004254312]	likely benign	17	43016356	43016356	Human		name
405806398	CV3348835	single nucleotide variant	NM_006373.4(VAT1):c.1134G>T (p.Lys378Asn)	not specified [RCV004480167]	uncertain significance	17	43016109	43016109	Human		name
407529398	CV3493336	single nucleotide variant	NM_006373.4(VAT1):c.1153C>G (p.Leu385Val)	not specified [RCV004680888]	uncertain significance	17	43016090	43016090	Human		name
598205483	CV3929420	single nucleotide variant	NM_006373.4(VAT1):c.1003G>A (p.Val335Met)	not specified [RCV005290859]	uncertain significance	17	43016402	43016402	Human		name
598240091	CV3929421	single nucleotide variant	NM_006373.4(VAT1):c.1093G>A (p.Glu365Lys)	not specified [RCV005296712]	uncertain significance	17	43016312	43016312	Human		name
598205490	CV3929423	single nucleotide variant	NM_006373.4(VAT1):c.1127A>C (p.Glu376Ala)	not specified [RCV005290860]	uncertain significance	17	43016116	43016116	Human		name
8585149	CV119730	single nucleotide variant	NM_020927.2(VAT1L):c.234-4296A>G	Lung cancer [RCV000100250]	uncertain significance	16	77812625	77812625	Human		name
8585150	CV119731	single nucleotide variant	NM_020927.2(VAT1L):c.579+3538G>A	Lung cancer [RCV000100251]	uncertain significance	16	77828999	77828999	Human		name
8585151	CV119732	single nucleotide variant	NM_020927.2(VAT1L):c.1077+40420G>C	Lung cancer [RCV000100252]	uncertain significance	16	77925222	77925222	Human		name
156047203	CV2382417	single nucleotide variant	NM_020927.3(VAT1L):c.26C>A (p.Ala9Glu)	not specified [RCV004230756]	uncertain significance	16	77788708	77788708	Human		name
405806418	CV3348844	single nucleotide variant	NM_020927.3(VAT1L):c.16G>A (p.Val6Met)	not specified [RCV004480176]	uncertain significance	16	77788698	77788698	Human		name
401775533	CV2710605	single nucleotide variant	NM_020927.3(VAT1L):c.95G>C (p.Gly32Ala)	not specified [RCV004319521]	uncertain significance	16	77788777	77788777	Human		name
405806420	CV3348845	single nucleotide variant	NM_020927.3(VAT1L):c.44T>A (p.Met15Lys)	not specified [RCV004480177]	uncertain significance	16	77788726	77788726	Human		name
405806432	CV3348851	single nucleotide variant	NM_020927.3(VAT1L):c.94G>A (p.Gly32Ser)	not specified [RCV004480183]	uncertain significance	16	77788776	77788776	Human		name
407529406	CV3493341	single nucleotide variant	NM_020927.3(VAT1L):c.89G>A (p.Gly30Asp)	not specified [RCV004680892]	uncertain significance	16	77788771	77788771	Human		name
156080319	CV2198456	single nucleotide variant	NM_020927.3(VAT1L):c.293C>G (p.Thr98Ser)	not specified [RCV004081984]	uncertain significance	16	77816980	77816980	Human		name
156033274	CV2376575	single nucleotide variant	NM_020927.3(VAT1L):c.115G>A (p.Ala39Thr)	not specified [RCV004220738]	uncertain significance	16	77788797	77788797	Human		name
329399249	CV2436474	single nucleotide variant	NM_020927.3(VAT1L):c.106C>T (p.Leu36Phe)	not specified [RCV004251854]	uncertain significance	16	77788788	77788788	Human		name
401771499	CV2686201	single nucleotide variant	NM_020927.3(VAT1L):c.116C>T (p.Ala39Val)	not specified [RCV004297296]	uncertain significance	16	77788798	77788798	Human		name
407529403	CV3493339	single nucleotide variant	NM_020927.3(VAT1L):c.109G>A (p.Gly37Arg)	not specified [RCV004680890]	uncertain significance	16	77788791	77788791	Human		name
597697898	CV3633192	single nucleotide variant	NM_020927.3(VAT1L):c.281A>C (p.Asn94Thr)	not specified [RCV004885318]	uncertain significance	16	77816968	77816968	Human		name
598205498	CV3929425	single nucleotide variant	NM_020927.3(VAT1L):c.257T>A (p.Met86Lys)	not specified [RCV005290861]	uncertain significance	16	77816944	77816944	Human		name
598240134	CV3929430	single nucleotide variant	NM_020927.3(VAT1L):c.262C>G (p.Arg88Gly)	not specified [RCV005296719]	uncertain significance	16	77816949	77816949	Human		name
598205506	CV3929431	single nucleotide variant	NM_020927.3(VAT1L):c.197C>G (p.Pro66Arg)	not specified [RCV005290862]	uncertain significance	16	77788879	77788879	Human		name
156176161	CV2254710	single nucleotide variant	NM_020927.3(VAT1L):c.706G>T (p.Val236Leu)	not specified [RCV004115187]	uncertain significance	16	77862874	77862874	Human		name
156279060	CV2297580	single nucleotide variant	NM_020927.3(VAT1L):c.861C>G (p.Ser287Arg)	not specified [RCV004155283]	uncertain significance	16	77879203	77879203	Human		name
155957970	CV2304228	single nucleotide variant	NM_020927.3(VAT1L):c.499A>G (p.Thr167Ala)	not specified [RCV004170248]	uncertain significance	16	77825381	77825381	Human		name
156100663	CV2313424	single nucleotide variant	NM_020927.3(VAT1L):c.610G>T (p.Val204Phe)	not specified [RCV004163744]	uncertain significance	16	77862778	77862778	Human		name
156364317	CV2341940	single nucleotide variant	NM_020927.3(VAT1L):c.803C>G (p.Pro268Arg)	not specified [RCV004184884]	uncertain significance	16	77876450	77876450	Human		name
156073362	CV2365450	single nucleotide variant	NM_020927.3(VAT1L):c.685T>G (p.Phe229Val)	not specified [RCV004209526]	uncertain significance	16	77862853	77862853	Human		name
401758321	CV2704424	single nucleotide variant	NM_020927.3(VAT1L):c.749T>A (p.Val250Asp)	not specified [RCV004311387]	uncertain significance	16	77876396	77876396	Human		name
401770237	CV2711007	single nucleotide variant	NM_020927.3(VAT1L):c.535C>T (p.Arg179Trp)	not specified [RCV004310710]	uncertain significance	16	77825417	77825417	Human		name
401891292	CV2779324	single nucleotide variant	NM_020927.3(VAT1L):c.994C>T (p.Arg332Trp)	not specified [RCV004350990]	uncertain significance	16	77884719	77884719	Human		name
405806422	CV3348846	single nucleotide variant	NM_020927.3(VAT1L):c.469G>A (p.Glu157Lys)	not specified [RCV004480178]	uncertain significance	16	77825351	77825351	Human		name
405806424	CV3348847	single nucleotide variant	NM_020927.3(VAT1L):c.638C>G (p.Ala213Gly)	not specified [RCV004480179]	uncertain significance	16	77862806	77862806	Human		name
405806426	CV3348848	single nucleotide variant	NM_020927.3(VAT1L):c.727T>C (p.Ser243Pro)	not specified [RCV004480180]	uncertain significance	16	77876374	77876374	Human		name
405806428	CV3348849	single nucleotide variant	NM_020927.3(VAT1L):c.833C>G (p.Ser278Cys)	not specified [RCV004480181]	uncertain significance	16	77879175	77879175	Human		name
405806430	CV3348850	single nucleotide variant	NM_020927.3(VAT1L):c.838A>G (p.Met280Val)	not specified [RCV004480182]	uncertain significance	16	77879180	77879180	Human		name
407464786	CV3493337	single nucleotide variant	NM_020927.3(VAT1L):c.715G>A (p.Val239Ile)	not specified [RCV004688598]	uncertain significance	16	77862883	77862883	Human		name
407529400	CV3493338	single nucleotide variant	NM_020927.3(VAT1L):c.373C>G (p.Arg125Gly)	not specified [RCV004680889]	uncertain significance	16	77825255	77825255	Human		name
597803671	CV3633195	single nucleotide variant	NM_020927.3(VAT1L):c.535C>G (p.Arg179Gly)	not specified [RCV004881856]	uncertain significance	16	77825417	77825417	Human		name
597697916	CV3633196	single nucleotide variant	NM_020927.3(VAT1L):c.359A>G (p.Tyr120Cys)	not specified [RCV004885320]	uncertain significance	16	77817046	77817046	Human		name
598240110	CV3929426	single nucleotide variant	NM_020927.3(VAT1L):c.545T>A (p.Met182Lys)	not specified [RCV005296715]	uncertain significance	16	77825427	77825427	Human		name
598240118	CV3929427	single nucleotide variant	NM_020927.3(VAT1L):c.802C>A (p.Pro268Thr)	not specified [RCV005296716]	uncertain significance	16	77876449	77876449	Human		name
156378658	CV2207774	single nucleotide variant	NM_020927.3(VAT1L):c.1016T>C (p.Ile339Thr)	not specified [RCV004084211]	uncertain significance	16	77884741	77884741	Human		name
156029533	CV2238323	single nucleotide variant	NM_020927.3(VAT1L):c.1219G>A (p.Gly407Arg)	not specified [RCV004113398]	uncertain significance	16	77977654	77977654	Human		name
156037771	CV2250282	single nucleotide variant	NM_020927.3(VAT1L):c.1175G>A (p.Ser392Asn)	not specified [RCV004117062]	uncertain significance	16	77977610	77977610	Human		name
156176277	CV2299797	single nucleotide variant	NM_020927.3(VAT1L):c.1224C>A (p.Asp408Glu)	not specified [RCV004148952]	uncertain significance	16	77977659	77977659	Human		name
156361174	CV2326405	single nucleotide variant	NM_020927.3(VAT1L):c.1012C>A (p.Leu338Ile)	not specified [RCV004182979]	uncertain significance	16	77884737	77884737	Human		name
401772666	CV2719718	single nucleotide variant	NM_020927.3(VAT1L):c.1042A>C (p.Lys348Gln)	not specified [RCV004329158]	uncertain significance	16	77884767	77884767	Human		name
405806409	CV3348840	single nucleotide variant	NM_020927.3(VAT1L):c.1206G>T (p.Glu402Asp)	not specified [RCV004480172]	uncertain significance	16	77977641	77977641	Human		name
405806414	CV3348842	single nucleotide variant	NM_020927.3(VAT1L):c.1228G>A (p.Glu410Lys)	not specified [RCV004480174]	uncertain significance	16	77977663	77977663	Human		name
405806416	CV3348843	single nucleotide variant	NM_020927.3(VAT1L):c.1241G>A (p.Arg414Gln)	not specified [RCV004480175]	uncertain significance	16	77977676	77977676	Human		name
407529409	CV3493342	single nucleotide variant	NM_020927.3(VAT1L):c.1165G>A (p.Ala389Thr)	not specified [RCV004680893]	uncertain significance	16	77977600	77977600	Human		name
598240124	CV3929428	single nucleotide variant	NM_020927.3(VAT1L):c.1118T>C (p.Ile373Thr)	not specified [RCV005296717]	uncertain significance	16	77971890	77971890	Human		name
598240130	CV3929429	single nucleotide variant	NM_020927.3(VAT1L):c.1157C>A (p.Pro386Gln)	not specified [RCV005296718]	uncertain significance	16	77971929	77971929	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