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71 records found for search term Golga1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15119492CV744509single nucleotide variantNM_002077.4(GOLGA1):c.1497+8C>Gnot provided [RCV000895736]benign9124890381124890381Humanname
405769037CV3262204single nucleotide variantNM_002077.4(GOLGA1):c.31G>A (p.Glu11Lys)not specified [RCV004395594]uncertain significance9124938681124938681Humanname
156333951CV2266969single nucleotide variantNM_002077.4(GOLGA1):c.118G>A (p.Asp40Asn)not specified [RCV004131621]uncertain significance9124938594124938594Humanname
156034084CV2338586single nucleotide variantNM_002077.4(GOLGA1):c.220C>A (p.Leu74Ile)not specified [RCV004182177]uncertain significance9124931322124931322Humanname
401728446CV2686096single nucleotide variantNM_002077.4(GOLGA1):c.191A>G (p.Asn64Ser)not specified [RCV004297105]uncertain significance9124931351124931351Humanname
405769001CV3262198single nucleotide variantNM_002077.4(GOLGA1):c.1641C>T (p.Ala547=)not specified [RCV004395588]likely benign9124889263124889263Humanname
405769019CV3262201single nucleotide variantNM_002077.4(GOLGA1):c.202C>T (p.Arg68Trp)not specified [RCV004395591]uncertain significance9124931340124931340Humanname
407520282CV3439694single nucleotide variantNM_002077.4(GOLGA1):c.241G>T (p.Val81Phe)not specified [RCV004629942]uncertain significance9124929276124929276Humanname
597788572CV3678340single nucleotide variantNM_002077.4(GOLGA1):c.142G>A (p.Asp48Asn)not specified [RCV004932777]uncertain significance9124931400124931400Humanname
597730830CV3678344single nucleotide variantNM_002077.4(GOLGA1):c.155C>G (p.Ser52Cys)not specified [RCV004919857]uncertain significance9124931387124931387Humanname
15193562CV700794single nucleotide variantNM_002077.4(GOLGA1):c.1806T>G (p.Thr602=)not provided [RCV000955406]benign9124888352124888352Humanname
15198422CV700795single nucleotide variantNM_002077.4(GOLGA1):c.1734C>T (p.Ala578=)not provided [RCV000956751]benign9124889170124889170Humanname
156069807CV2203852single nucleotide variantNM_002077.4(GOLGA1):c.844G>T (p.Val282Phe)not specified [RCV004069913]uncertain significance9124912026124912026Humanname
156022927CV2223341single nucleotide variantNM_002077.4(GOLGA1):c.764A>C (p.Glu255Ala)not specified [RCV004105944]uncertain significance9124921208124921208Humanname
156215475CV2257579single nucleotide variantNM_002077.4(GOLGA1):c.640G>A (p.Glu214Lys)not specified [RCV004127412]uncertain significance9124921814124921814Humanname
156130004CV2364812single nucleotide variantNM_002077.4(GOLGA1):c.916A>G (p.Arg306Gly)not specified [RCV004219678]uncertain significance9124911954124911954Humanname
329387693CV2470906single nucleotide variantNM_002077.4(GOLGA1):c.475C>G (p.Gln159Glu)not specified [RCV004276103]uncertain significance9124923181124923181Humanname
405769030CV3262203single nucleotide variantNM_002077.4(GOLGA1):c.305C>T (p.Ser102Phe)not specified [RCV004395593]uncertain significance9124928282124928282Humanname
405769042CV3262205single nucleotide variantNM_002077.4(GOLGA1):c.559A>C (p.Met187Leu)not specified [RCV004395595]uncertain significance9124923097124923097Humanname
407520278CV3439695single nucleotide variantNM_002077.4(GOLGA1):c.796C>A (p.Gln266Lys)not specified [RCV004629943]uncertain significance9124921176124921176Humanname
597788568CV3678339single nucleotide variantNM_002077.4(GOLGA1):c.443T>C (p.Ile148Thr)not specified [RCV004932776]uncertain significance9124923213124923213Humanname
597788670CV3678342single nucleotide variantNM_002077.4(GOLGA1):c.941A>G (p.Glu314Gly)not specified [RCV004932779]uncertain significance9124911929124911929Humanname
597730842CV3678345single nucleotide variantNM_002077.4(GOLGA1):c.716C>T (p.Thr239Met)not specified [RCV004919858]uncertain significance9124921738124921738Humanname
597730854CV3678346single nucleotide variantNM_002077.4(GOLGA1):c.490T>C (p.Phe164Leu)not specified [RCV004919859]uncertain significance9124923166124923166Humanname
597730895CV3678352single nucleotide variantNM_002077.4(GOLGA1):c.701A>G (p.Gln234Arg)not specified [RCV004919863]uncertain significance9124921753124921753Humanname
597730913CV3678355single nucleotide variantNM_002077.4(GOLGA1):c.919C>A (p.Leu307Ile)not specified [RCV004919865]uncertain significance9124911951124911951Humanname
598264356CV3974443single nucleotide variantNM_002077.4(GOLGA1):c.829A>G (p.Ile277Val)not specified [RCV005348835]uncertain significance9124921143124921143Humanname
156131076CV2235209single nucleotide variantNM_002077.4(GOLGA1):c.2237G>C (p.Gly746Ala)not specified [RCV004107261]uncertain significance9124880597124880597Humanname
156270251CV2276571single nucleotide variantNM_002077.4(GOLGA1):c.1163C>T (p.Ala388Val)not specified [RCV004146062]likely benign9124899477124899477Humanname
155918435CV2283545single nucleotide variantNM_002077.4(GOLGA1):c.1287C>A (p.Asp429Glu)not specified [RCV004139754]uncertain significance9124899353124899353Humanname
156003537CV2295694single nucleotide variantNM_002077.4(GOLGA1):c.1648G>C (p.Glu550Gln)not specified [RCV004149844]uncertain significance9124889256124889256Humanname
156288969CV2327459single nucleotide variantNM_002077.4(GOLGA1):c.1366C>T (p.Arg456Cys)not specified [RCV004174873]uncertain significance9124898590124898590Humanname
156124921CV2350146single nucleotide variantNM_002077.4(GOLGA1):c.1544G>A (p.Arg515Gln)not specified [RCV004200066]likely benign9124889490124889490Humanname
155909746CV2359962single nucleotide variantNM_002077.4(GOLGA1):c.2000G>A (p.Arg667Gln)not specified [RCV004212805]uncertain significance9124881920124881920Humanname
156197767CV2362731single nucleotide variantNM_002077.4(GOLGA1):c.1036G>A (p.Ala346Thr)not specified [RCV004208850]uncertain significance9124908406124908406Humanname
156341210CV2368375single nucleotide variantNM_002077.4(GOLGA1):c.2255A>G (p.Lys752Arg)not specified [RCV004219149]uncertain significance9124880579124880579Humanname
329368708CV2453234single nucleotide variantNM_002077.4(GOLGA1):c.1552A>G (p.Thr518Ala)not specified [RCV004266880]uncertain significance9124889482124889482Humanname
401764396CV2727931single nucleotide variantNM_002077.4(GOLGA1):c.2287C>T (p.Arg763Trp)not specified [RCV004324111]uncertain significance9124880547124880547Humanname
401884472CV2761753single nucleotide variantNM_002077.4(GOLGA1):c.1019C>T (p.Ala340Val)not specified [RCV004339406]uncertain significance9124908423124908423Humanname
401863846CV2770863single nucleotide variantNM_002077.4(GOLGA1):c.1607A>G (p.Asn536Ser)not specified [RCV004343540]uncertain significance9124889297124889297Humanname
405768978CV3262194single nucleotide variantNM_002077.4(GOLGA1):c.1144A>G (p.Thr382Ala)not specified [RCV004395584]likely benign9124900469124900469Humanname
405768983CV3262195single nucleotide variantNM_002077.4(GOLGA1):c.1406A>C (p.Lys469Thr)not specified [RCV004395585]uncertain significance9124898550124898550Humanname
405768989CV3262196single nucleotide variantNM_002077.4(GOLGA1):c.1415G>T (p.Trp472Leu)not specified [RCV004395586]uncertain significance9124890471124890471Humanname
405768994CV3262197single nucleotide variantNM_002077.4(GOLGA1):c.1555G>A (p.Glu519Lys)not specified [RCV004395587]uncertain significance9124889479124889479Humanname
405769007CV3262199single nucleotide variantNM_002077.4(GOLGA1):c.1863G>C (p.Lys621Asn)not specified [RCV004395589]uncertain significance9124888295124888295Humanname
405769013CV3262200single nucleotide variantNM_002077.4(GOLGA1):c.2021T>C (p.Met674Thr)not specified [RCV004395590]uncertain significance9124881899124881899Humanname
405769024CV3262202single nucleotide variantNM_002077.4(GOLGA1):c.2035C>T (p.Pro679Ser)not specified [RCV004395592]uncertain significance9124881885124881885Humanname
407520306CV3439687single nucleotide variantNM_002077.4(GOLGA1):c.1644G>C (p.Glu548Asp)not specified [RCV004629935]uncertain significance9124889260124889260Humanname
407520303CV3439688single nucleotide variantNM_002077.4(GOLGA1):c.2020A>T (p.Met674Leu)not specified [RCV004629936]uncertain significance9124881900124881900Humanname
407520299CV3439689single nucleotide variantNM_002077.4(GOLGA1):c.1241C>T (p.Ala414Val)not specified [RCV004629937]uncertain significance9124899399124899399Humanname
407520292CV3439691single nucleotide variantNM_002077.4(GOLGA1):c.1553C>A (p.Thr518Asn)not specified [RCV004629939]uncertain significance9124889481124889481Humanname
407520288CV3439692single nucleotide variantNM_002077.4(GOLGA1):c.2187G>C (p.Glu729Asp)not specified [RCV004629940]uncertain significance9124881207124881207Humanname
407520285CV3439693single nucleotide variantNM_002077.4(GOLGA1):c.1132G>A (p.Ala378Thr)not specified [RCV004629941]uncertain significance9124900481124900481Humanname
407520274CV3439696single nucleotide variantNM_002077.4(GOLGA1):c.1757C>T (p.Ser586Leu)not specified [RCV004629944]uncertain significance9124889147124889147Humanname
407520270CV3439697single nucleotide variantNM_002077.4(GOLGA1):c.2299T>C (p.Ser767Pro)not specified [RCV004629945]uncertain significance9124880535124880535Humanname
597788565CV3678338single nucleotide variantNM_002077.4(GOLGA1):c.1681G>A (p.Ala561Thr)not specified [RCV004932775]uncertain significance9124889223124889223Humanname
597788673CV3678343single nucleotide variantNM_002077.4(GOLGA1):c.1718G>A (p.Arg573Gln)not specified [RCV004932780]likely benign9124889186124889186Humanname
597730865CV3678347single nucleotide variantNM_002077.4(GOLGA1):c.1009C>G (p.Gln337Glu)not specified [RCV004919860]uncertain significance9124908433124908433Humanname
597730875CV3678348single nucleotide variantNM_002077.4(GOLGA1):c.1514C>A (p.Ala505Asp)not specified [RCV004919861]uncertain significance9124889520124889520Humanname
597788677CV3678349single nucleotide variantNM_002077.4(GOLGA1):c.1469G>A (p.Arg490Gln)not specified [RCV004932781]uncertain significance9124890417124890417Humanname
597788680CV3678350single nucleotide variantNM_002077.4(GOLGA1):c.1064G>A (p.Arg355Gln)not specified [RCV004932782]uncertain significance9124908378124908378Humanname
597730885CV3678351single nucleotide variantNM_002077.4(GOLGA1):c.1361A>G (p.Tyr454Cys)not specified [RCV004919862]likely benign9124898595124898595Humanname
597788684CV3678353single nucleotide variantNM_002077.4(GOLGA1):c.1778T>C (p.Met593Thr)not specified [RCV004932783]uncertain significance9124888380124888380Humanname
597730906CV3678354single nucleotide variantNM_002077.4(GOLGA1):c.1283C>G (p.Ala428Gly)not specified [RCV004919864]uncertain significance9124899357124899357Humanname
597730922CV3678356single nucleotide variantNM_002077.4(GOLGA1):c.1598G>A (p.Arg533Gln)not specified [RCV004919866]likely benign9124889436124889436Humanname
598264330CV3974437single nucleotide variantNM_002077.4(GOLGA1):c.1232G>A (p.Arg411His)not specified [RCV005348830]uncertain significance9124899408124899408Humanname
598264334CV3974438single nucleotide variantNM_002077.4(GOLGA1):c.1525G>A (p.Glu509Lys)not specified [RCV005348831]uncertain significance9124889509124889509Humanname
598264339CV3974439single nucleotide variantNM_002077.4(GOLGA1):c.1478G>A (p.Arg493Lys)not specified [RCV005348832]uncertain significance9124890408124890408Humanname
598232850CV3974440single nucleotide variantNM_002077.4(GOLGA1):c.1108C>A (p.Leu370Ile)not specified [RCV005342666]uncertain significance9124900505124900505Humanname
598264345CV3974441single nucleotide variantNM_002077.4(GOLGA1):c.1116G>C (p.Gln372His)not specified [RCV005348833]uncertain significance9124900497124900497Humanname
598232856CV3974444single nucleotide variantNM_002077.4(GOLGA1):c.1627C>A (p.His543Asn)not specified [RCV005342667]uncertain significance9124889277124889277Humanname