Tigd2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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39 records found for search term Tigd2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401734932	CV2690718	single nucleotide variant	NM_145715.3(TIGD2):c.70G>A (p.Glu24Lys)	not specified [RCV004298443]	uncertain significance	4	89113044	89113044	Human		name
156138600	CV2280686	single nucleotide variant	NM_145715.3(TIGD2):c.136A>G (p.Lys46Glu)	not specified [RCV004143150]	uncertain significance	4	89113110	89113110	Human		name
401896880	CV2788901	single nucleotide variant	NM_145715.3(TIGD2):c.107G>C (p.Gly36Ala)	not specified [RCV004362938]	uncertain significance	4	89113081	89113081	Human		name
407520350	CV3475644	single nucleotide variant	NM_145715.3(TIGD2):c.268C>A (p.Gln90Lys)	not specified [RCV004676922]	uncertain significance	4	89113242	89113242	Human		name
156268023	CV2198870	single nucleotide variant	NM_145715.3(TIGD2):c.470G>A (p.Gly157Asp)	not specified [RCV004077905]	uncertain significance	4	89113444	89113444	Human		name
329385637	CV2462126	single nucleotide variant	NM_145715.3(TIGD2):c.346G>A (p.Glu116Lys)	not specified [RCV004266151]	uncertain significance	4	89113320	89113320	Human		name
401733952	CV2697912	single nucleotide variant	NM_145715.3(TIGD2):c.599C>T (p.Ser200Phe)	not specified [RCV004300619]	uncertain significance	4	89113573	89113573	Human		name
401759326	CV2708588	single nucleotide variant	NM_145715.3(TIGD2):c.334G>A (p.Ala112Thr)	not specified [RCV004307579]	uncertain significance	4	89113308	89113308	Human		name
401740129	CV2709828	single nucleotide variant	NM_145715.3(TIGD2):c.643G>A (p.Ala215Thr)	not specified [RCV004320803]	uncertain significance	4	89113617	89113617	Human		name
405752287	CV3335865	single nucleotide variant	NM_145715.3(TIGD2):c.359A>G (p.Asn120Ser)	not specified [RCV004467283]	uncertain significance	4	89113333	89113333	Human		name
405752294	CV3335866	single nucleotide variant	NM_145715.3(TIGD2):c.551A>G (p.Lys184Arg)	not specified [RCV004467284]	uncertain significance	4	89113525	89113525	Human		name
405752302	CV3335867	single nucleotide variant	NM_145715.3(TIGD2):c.598T>C (p.Ser200Pro)	not specified [RCV004467285]	uncertain significance	4	89113572	89113572	Human		name
407520339	CV3475640	single nucleotide variant	NM_145715.3(TIGD2):c.784T>C (p.Phe262Leu)	not specified [RCV004676918]	uncertain significance	4	89113758	89113758	Human		name
407520345	CV3475642	single nucleotide variant	NM_145715.3(TIGD2):c.582A>C (p.Glu194Asp)	not specified [RCV004676920]	uncertain significance	4	89113556	89113556	Human		name
597764288	CV3613384	single nucleotide variant	NM_145715.3(TIGD2):c.760G>C (p.Gly254Arg)	not specified [RCV004870069]	uncertain significance	4	89113734	89113734	Human		name
597764298	CV3613387	single nucleotide variant	NM_145715.3(TIGD2):c.623G>C (p.Arg208Thr)	not specified [RCV004870072]	uncertain significance	4	89113597	89113597	Human		name
598197415	CV3924183	single nucleotide variant	NM_145715.3(TIGD2):c.448A>G (p.Thr150Ala)	not specified [RCV005289576]	uncertain significance	4	89113422	89113422	Human		name
598176520	CV3924185	single nucleotide variant	NM_145715.3(TIGD2):c.622A>G (p.Arg208Gly)	not specified [RCV005285651]	uncertain significance	4	89113596	89113596	Human		name
156242834	CV2210784	single nucleotide variant	NM_145715.3(TIGD2):c.1426A>G (p.Ile476Val)	not specified [RCV004085877]	uncertain significance	4	89114400	89114400	Human		name
156042833	CV2311006	single nucleotide variant	NM_145715.3(TIGD2):c.1375C>A (p.Gln459Lys)	not specified [RCV004164028]	uncertain significance	4	89114349	89114349	Human		name
156043878	CV2342352	single nucleotide variant	NM_145715.3(TIGD2):c.1223C>A (p.Ala408Asp)	not specified [RCV004191918]	uncertain significance	4	89114197	89114197	Human		name
155928198	CV2391674	single nucleotide variant	NM_145715.3(TIGD2):c.1199T>C (p.Ile400Thr)	not specified [RCV004241832]	uncertain significance	4	89114173	89114173	Human		name
329398801	CV2442838	single nucleotide variant	NM_145715.3(TIGD2):c.1550A>G (p.Gln517Arg)	not specified [RCV004253451]	uncertain significance	4	89114524	89114524	Human		name
401750084	CV2719507	single nucleotide variant	NM_145715.3(TIGD2):c.1439C>T (p.Ala480Val)	not specified [RCV004326899]	uncertain significance	4	89114413	89114413	Human		name
401861292	CV2755526	single nucleotide variant	NM_145715.3(TIGD2):c.1273A>G (p.Ile425Val)	not specified [RCV004340109]	uncertain significance	4	89114247	89114247	Human		name
401871592	CV2783549	single nucleotide variant	NM_145715.3(TIGD2):c.1453A>G (p.Thr485Ala)	not specified [RCV004365878]	uncertain significance	4	89114427	89114427	Human		name
401898907	CV2792107	single nucleotide variant	NM_145715.3(TIGD2):c.1487A>G (p.Asp496Gly)	not specified [RCV004361333]	uncertain significance	4	89114461	89114461	Human		name
405752089	CV3335861	single nucleotide variant	NM_145715.3(TIGD2):c.1265A>G (p.His422Arg)	not specified [RCV004467279]	uncertain significance	4	89114239	89114239	Human		name
405752097	CV3335862	single nucleotide variant	NM_145715.3(TIGD2):c.1274T>C (p.Ile425Thr)	not specified [RCV004467280]	uncertain significance	4	89114248	89114248	Human		name
405752105	CV3335863	single nucleotide variant	NM_145715.3(TIGD2):c.1459A>C (p.Asn487His)	not specified [RCV004467281]	uncertain significance	4	89114433	89114433	Human		name
405752112	CV3335864	single nucleotide variant	NM_145715.3(TIGD2):c.1469A>T (p.Asp490Val)	not specified [RCV004467282]	uncertain significance	4	89114443	89114443	Human		name
407520342	CV3475641	single nucleotide variant	NM_145715.3(TIGD2):c.1177G>C (p.Glu393Gln)	not specified [RCV004676919]	uncertain significance	4	89114151	89114151	Human		name
407520348	CV3475643	single nucleotide variant	NM_145715.3(TIGD2):c.1265A>C (p.His422Pro)	not specified [RCV004676921]	uncertain significance	4	89114239	89114239	Human		name
597764284	CV3613383	single nucleotide variant	NM_145715.3(TIGD2):c.1572T>G (p.Asn524Lys)	not specified [RCV004870068]	uncertain significance	4	89114546	89114546	Human		name
597764292	CV3613385	single nucleotide variant	NM_145715.3(TIGD2):c.1085T>C (p.Val362Ala)	not specified [RCV004870070]	uncertain significance	4	89114059	89114059	Human		name
597764296	CV3613386	single nucleotide variant	NM_145715.3(TIGD2):c.1149A>C (p.Lys383Asn)	not specified [RCV004870071]	uncertain significance	4	89114123	89114123	Human		name
598197407	CV3924181	single nucleotide variant	NM_145715.3(TIGD2):c.1043A>T (p.Asp348Val)	not specified [RCV005289575]	uncertain significance	4	89114017	89114017	Human		name
598176515	CV3924182	single nucleotide variant	NM_145715.3(TIGD2):c.1273A>C (p.Ile425Leu)	not specified [RCV005285650]	uncertain significance	4	89114247	89114247	Human		name
598197430	CV3924186	single nucleotide variant	NM_145715.3(TIGD2):c.1207G>A (p.Gly403Arg)	not specified [RCV005289578]	uncertain significance	4	89114181	89114181	Human		name

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