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Variants search result for Homo sapiens
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63 records found for search term Gapdh
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
150448491CV1253559single nucleotide variantNM_002046.7(GAPDH):c.-8C>Gnot provided [RCV001667487]benign1265348256534825Humanname
597754313CV3680840single nucleotide variantNM_002046.7(GAPDH):c.30A>T (p.Gly10=)not specified [RCV004924344]likely benign1265364946536494Humanname
598203778CV3974017single nucleotide variantNM_002046.7(GAPDH):c.83T>G (p.Val28Gly)not specified [RCV005337319]uncertain significance1265365476536547Humanname
155942382CV2301165single nucleotide variantNM_002046.7(GAPDH):c.968G>A (p.Arg323Lys)not specified [RCV004160074]uncertain significance1265381306538130Humanname
401719219CV2679458single nucleotide variantNM_002046.7(GAPDH):c.494A>G (p.His165Arg)not specified [RCV004285979]uncertain significance1265373596537359Humanname
401887260CV2773267single nucleotide variantNM_002046.7(GAPDH):c.355G>T (p.Val119Phe)not specified [RCV004353939]uncertain significance1265371286537128Humanname
405750706CV3251157single nucleotide variantNM_002046.7(GAPDH):c.354G>T (p.Arg118Ser)not specified [RCV004392694]uncertain significance1265371276537127Humanname
405750713CV3251158single nucleotide variantNM_002046.7(GAPDH):c.755C>G (p.Pro252Arg)not specified [RCV004392695]uncertain significance1265378136537813Humanname
598203784CV3974018single nucleotide variantNM_002046.7(GAPDH):c.793G>A (p.Ala265Thr)not specified [RCV005337320]uncertain significance1265378516537851Humanname
401727969CV2678621single nucleotide variantNM_014364.5(GAPDHS):c.19G>A (p.Val7Ile)not specified [RCV004292622]uncertain significance193553354635533546Humanname
155916809CV2202028single nucleotide variantNM_014364.5(GAPDHS):c.86C>A (p.Pro29Gln)not specified [RCV004075949]uncertain significance193553683135536831Humanname
405750777CV3251167single nucleotide variantNM_014364.5(GAPDHS):c.86C>T (p.Pro29Leu)not specified [RCV004392704]uncertain significance193553683135536831Humanname
407462141CV3436371single nucleotide variantNM_014364.5(GAPDHS):c.31G>A (p.Val11Ile)not specified [RCV004634453]uncertain significance193553355835533558Humanname
407462154CV3436376single nucleotide variantNM_014364.5(GAPDHS):c.74G>C (p.Arg25Thr)not specified [RCV004634458]uncertain significance193553681935536819Humanname
15182122CV728113single nucleotide variantNM_014364.5(GAPDHS):c.858G>A (p.Ala286=)not provided [RCV000885919]benign193554345635543456Humanname
155917596CV2199005single nucleotide variantNM_014364.5(GAPDHS):c.115C>G (p.Gln39Glu)not specified [RCV004080415]uncertain significance193553686035536860Humanname
156141918CV2208469single nucleotide variantNM_014364.5(GAPDHS):c.170C>T (p.Pro57Leu)not specified [RCV004091006]uncertain significance193553691535536915Humanname
156030580CV2238416single nucleotide variantNM_014364.5(GAPDHS):c.263G>A (p.Arg88His)not specified [RCV004113479]uncertain significance193553832435538324Humanname
156002981CV2347741single nucleotide variantNM_014364.5(GAPDHS):c.109G>C (p.Glu37Gln)not specified [RCV004202708]uncertain significance193553685435536854Humanname
156258886CV2395429single nucleotide variantNM_014364.5(GAPDHS):c.247T>C (p.Phe83Leu)not specified [RCV004241302]uncertain significance193553830835538308Humanname
401767098CV2681429single nucleotide variantNM_014364.5(GAPDHS):c.274C>T (p.Arg92Cys)not specified [RCV004291972]uncertain significance193553833535538335Humanname
401861427CV2759572single nucleotide variantNM_014364.5(GAPDHS):c.197C>T (p.Pro66Leu)not specified [RCV004338550]uncertain significance193553694235536942Humanname
405750747CV3251163single nucleotide variantNM_014364.5(GAPDHS):c.220C>T (p.Arg74Trp)not specified [RCV004392700]uncertain significance193553696535536965Humanname
405750753CV3251164single nucleotide variantNM_014364.5(GAPDHS):c.221G>A (p.Arg74Gln)not specified [RCV004392701]uncertain significance193553696635536966Humanname
407462149CV3436374single nucleotide variantNM_014364.5(GAPDHS):c.128A>G (p.Glu43Gly)not specified [RCV004634456]uncertain significance193553687335536873Humanname
407462152CV3436375single nucleotide variantNM_014364.5(GAPDHS):c.124C>T (p.Pro42Ser)not specified [RCV004634457]uncertain significance193553686935536869Humanname
407462157CV3436377single nucleotide variantNM_014364.5(GAPDHS):c.134C>T (p.Thr45Ile)not specified [RCV004634459]uncertain significance193553687935536879Humanname
597754323CV3680843single nucleotide variantNM_014364.5(GAPDHS):c.259G>A (p.Gly87Ser)not specified [RCV004924346]uncertain significance193553832035538320Humanname
156176646CV2205339single nucleotide variantNM_014364.5(GAPDHS):c.484G>A (p.Gly162Arg)not specified [RCV004079953]uncertain significance193554235335542353Humanname
156242835CV2231462single nucleotide variantNM_014364.5(GAPDHS):c.784G>A (p.Gly262Arg)not specified [RCV004096534]uncertain significance193554338235543382Humanname
156285155CV2232780single nucleotide variantNM_014364.5(GAPDHS):c.357G>T (p.Lys119Asn)not specified [RCV004101417]uncertain significance193553859135538591Humanname
156272512CV2297200single nucleotide variantNM_014364.5(GAPDHS):c.506C>G (p.Ser169Cys)not specified [RCV004151087]uncertain significance193554237535542375Humanname
156357660CV2318342single nucleotide variantNM_014364.5(GAPDHS):c.800C>T (p.Ala267Val)not specified [RCV004179505]uncertain significance193554339835543398Humanname
156153188CV2328508single nucleotide variantNM_014364.5(GAPDHS):c.964G>A (p.Ala322Thr)not specified [RCV004175883]uncertain significance193554373535543735Humanname
156104022CV2352420single nucleotide variantNM_014364.5(GAPDHS):c.941T>C (p.Val314Ala)not specified [RCV004200885]uncertain significance193554371235543712Humanname
156112417CV2353425single nucleotide variantNM_014364.5(GAPDHS):c.580G>A (p.Ala194Thr)not specified [RCV004205882]uncertain significance193554252935542529Humanname
155929429CV2363522single nucleotide variantNM_014364.5(GAPDHS):c.761C>T (p.Thr254Met)not specified [RCV004216093]uncertain significance193554335935543359Humanname
155985575CV2368131single nucleotide variantNM_014364.5(GAPDHS):c.496G>A (p.Val166Met)not specified [RCV004216479]uncertain significance193554236535542365Humanname
401778163CV2700652single nucleotide variantNM_014364.5(GAPDHS):c.982T>A (p.Ser328Thr)not specified [RCV004313372]uncertain significance193554375335543753Humanname
405750761CV3251165single nucleotide variantNM_014364.5(GAPDHS):c.806G>A (p.Arg269Gln)not specified [RCV004392702]uncertain significance193554340435543404Humanname
405750771CV3251166single nucleotide variantNM_014364.5(GAPDHS):c.856G>T (p.Ala286Ser)not specified [RCV004392703]uncertain significance193554345435543454Humanname
405750784CV3251168single nucleotide variantNM_014364.5(GAPDHS):c.943G>A (p.Val315Met)not specified [RCV004392705]uncertain significance193554371435543714Humanname
407462146CV3436373single nucleotide variantNM_014364.5(GAPDHS):c.665C>T (p.Ala222Val)not specified [RCV004634455]uncertain significance193554295035542950Humanname
597780135CV3680841single nucleotide variantNM_014364.5(GAPDHS):c.959G>A (p.Arg320His)not specified [RCV004930552]uncertain significance193554373035543730Humanname
597754319CV3680842single nucleotide variantNM_014364.5(GAPDHS):c.569T>C (p.Val190Ala)not specified [RCV004924345]uncertain significance193554251835542518Humanname
597754331CV3680845single nucleotide variantNM_014364.5(GAPDHS):c.653T>C (p.Ile218Thr)not specified [RCV004924348]uncertain significance193554260235542602Humanname
597754336CV3680846single nucleotide variantNM_014364.5(GAPDHS):c.607G>A (p.Val203Ile)not specified [RCV004924349]uncertain significance193554255635542556Humanname
597754339CV3680847single nucleotide variantNM_014364.5(GAPDHS):c.770A>C (p.Gln257Pro)not specified [RCV004924350]uncertain significance193554336835543368Humanname
597754344CV3680848single nucleotide variantNM_014364.5(GAPDHS):c.704T>G (p.Val235Gly)not specified [RCV004924351]uncertain significance193554298935542989Humanname
597780138CV3680849single nucleotide variantNM_014364.5(GAPDHS):c.781G>A (p.Asp261Asn)not specified [RCV004930553]uncertain significance193554337935543379Humanname
597754348CV3680850single nucleotide variantNM_014364.5(GAPDHS):c.596C>T (p.Ala199Val)not specified [RCV004924352]uncertain significance193554254535542545Humanname
598203790CV3974019single nucleotide variantNM_014364.5(GAPDHS):c.712G>A (p.Glu238Lys)not specified [RCV005337321]uncertain significance193554299735542997Humanname
598203796CV3974020single nucleotide variantNM_014364.5(GAPDHS):c.836T>C (p.Ile279Thr)not specified [RCV005337322]uncertain significance193554343435543434Humanname
598158888CV3974021single nucleotide variantNM_014364.5(GAPDHS):c.764C>G (p.Ala255Gly)not specified [RCV005328154]uncertain significance193554336235543362Humanname
598203802CV3974022single nucleotide variantNM_014364.5(GAPDHS):c.638C>T (p.Pro213Leu)not specified [RCV005337323]uncertain significance193554258735542587Humanname
15182117CV728112single nucleotide variantNM_014364.5(GAPDHS):c.601A>G (p.Met201Val)not provided [RCV000885918]benign193554255035542550Humanname
9686993CV171631single nucleotide variantNM_014364.5(GAPDHS):c.1129G>A (p.Asp377Asn)Prostate cancer [RCV000149212]uncertain significance193554498135544981Human2name
156132863CV2235358single nucleotide variantNM_014364.5(GAPDHS):c.1035C>G (p.Ile345Met)not specified [RCV004109426]uncertain significance193554380635543806Humanname
405750719CV3251159single nucleotide variantNM_014364.5(GAPDHS):c.1136T>C (p.Phe379Ser)not specified [RCV004392696]uncertain significance193554498835544988Humanname
405750729CV3251160single nucleotide variantNM_014364.5(GAPDHS):c.1139T>G (p.Val380Gly)not specified [RCV004392697]uncertain significance193554499135544991Humanname
405750736CV3251161single nucleotide variantNM_014364.5(GAPDHS):c.1208T>A (p.Met403Lys)not specified [RCV004392698]uncertain significance193554515135545151Humanname
405750743CV3251162single nucleotide variantNM_014364.5(GAPDHS):c.1209G>A (p.Met403Ile)not specified [RCV004392699]uncertain significance193554515235545152Humanname
597754327CV3680844single nucleotide variantNM_014364.5(GAPDHS):c.1046C>A (p.Thr349Asn)not specified [RCV004924347]uncertain significance193554381735543817Humanname