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Variants search result for Homo sapiens
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60 records found for search term Golga5
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
404979636CV2850177single nucleotide variantNM_005113.4(GOLGA5):c.772+1G>Tnot provided [RCV003487877]uncertain significance149280696492806964Humanname
8584134CV118706single nucleotide variantNM_005113.3(GOLGA5):c.545-2459G>TLung cancer [RCV000099226]uncertain significance149280427792804277Humanname
598232937CV3974506single nucleotide variantNM_005113.4(GOLGA5):c.91A>G (p.Asn31Asp)not specified [RCV005342680]uncertain significance149279752892797528Humanname
156179145CV2355989single nucleotide variantNM_005113.4(GOLGA5):c.165G>C (p.Gln55His)not specified [RCV004201368]uncertain significance149279760292797602Humanname
329354841CV2449110single nucleotide variantNM_005113.4(GOLGA5):c.119C>T (p.Thr40Ile)not specified [RCV004264172]uncertain significance149279755692797556Humanname
401773249CV2709208single nucleotide variantNM_005113.4(GOLGA5):c.160T>G (p.Tyr54Asp)not specified [RCV004316380]uncertain significance149279759792797597Humanname
401772040CV2712049single nucleotide variantNM_005113.4(GOLGA5):c.103A>G (p.Ile35Val)not specified [RCV004311468]uncertain significance149279754092797540Humanname
597731454CV3678451single nucleotide variantNM_005113.4(GOLGA5):c.152A>G (p.Asp51Gly)not specified [RCV004919922]uncertain significance149279758992797589Humanname
8635337CV90559single nucleotide variantNM_005113.3(GOLGA5):c.1611A>G (p.Arg537=)Malignant melanoma [RCV000070657]not provided149281982792819827Humanname
156071843CV2251448single nucleotide variantNM_005113.4(GOLGA5):c.603T>A (p.Asn201Lys)not specified [RCV004117427]uncertain significance149280679492806794Humanname
156033743CV2256509single nucleotide variantNM_005113.4(GOLGA5):c.632A>C (p.His211Pro)not specified [RCV004118712]uncertain significance149280682392806823Humanname
156059002CV2383480single nucleotide variantNM_005113.4(GOLGA5):c.521A>G (p.Asn174Ser)not specified [RCV004222492]uncertain significance149279795892797958Humanname
329393206CV2466779single nucleotide variantNM_005113.4(GOLGA5):c.655G>A (p.Gly219Ser)not specified [RCV004280729]likely benign149280684692806846Humanname
401749561CV2694674single nucleotide variantNM_005113.4(GOLGA5):c.724A>C (p.Asn242His)not specified [RCV004298779]uncertain significance149280691592806915Humanname
401741497CV2697562single nucleotide variantNM_005113.4(GOLGA5):c.953G>A (p.Arg318His)not specified [RCV004298318]uncertain significance149280948092809480Humanname
401889744CV2758426single nucleotide variantNM_005113.4(GOLGA5):c.314G>C (p.Arg105Thr)not specified [RCV004335080]uncertain significance149279775192797751Humanname
401880312CV2770046single nucleotide variantNM_005113.4(GOLGA5):c.331G>T (p.Val111Leu)not specified [RCV004353865]uncertain significance149279776892797768Humanname
405769615CV3262302single nucleotide variantNM_005113.4(GOLGA5):c.506A>G (p.Lys169Arg)not specified [RCV004395692]uncertain significance149279794392797943Humanname
405769627CV3262304single nucleotide variantNM_005113.4(GOLGA5):c.952C>T (p.Arg318Cys)not specified [RCV004395694]uncertain significance149280947992809479Humanname
407520195CV3439744single nucleotide variantNM_005113.4(GOLGA5):c.330T>G (p.Phe110Leu)not specified [RCV004629987]uncertain significance149279776792797767Humanname
407520198CV3439745single nucleotide variantNM_005113.4(GOLGA5):c.767A>G (p.Gln256Arg)not specified [RCV004629988]uncertain significance149280695892806958Humanname
407520207CV3439748single nucleotide variantNM_005113.4(GOLGA5):c.520A>C (p.Asn174His)not specified [RCV004629991]uncertain significance149279795792797957Humanname
597731466CV3678453single nucleotide variantNM_005113.4(GOLGA5):c.820T>C (p.Ser274Pro)not specified [RCV004919923]uncertain significance149280934792809347Humanname
597731485CV3678456single nucleotide variantNM_005113.4(GOLGA5):c.886G>A (p.Ala296Thr)not specified [RCV004919925]uncertain significance149280941392809413Humanname
598232943CV3974508single nucleotide variantNM_005113.4(GOLGA5):c.445G>C (p.Val149Leu)not specified [RCV005342681]uncertain significance149279788292797882Humanname
598264603CV3974509single nucleotide variantNM_005113.4(GOLGA5):c.695A>T (p.Gln232Leu)not specified [RCV005348886]uncertain significance149280688692806886Humanname
155978452CV2222689single nucleotide variantNM_005113.4(GOLGA5):c.1129G>A (p.Ala377Thr)not specified [RCV004101549]uncertain significance149281156392811563Humanname
156024988CV2273928single nucleotide variantNM_005113.4(GOLGA5):c.2109A>G (p.Ile703Met)not specified [RCV004134333]uncertain significance149283744392837443Humanname
155905342CV2303087single nucleotide variantNM_005113.4(GOLGA5):c.2050A>C (p.Ser684Arg)not specified [RCV004156870]uncertain significance149283566392835663Humanname
156106253CV2352596single nucleotide variantNM_005113.4(GOLGA5):c.1236G>T (p.Gln412His)not specified [RCV004203088]uncertain significance149281167092811670Humanname
155931159CV2362478single nucleotide variantNM_005113.4(GOLGA5):c.1994A>G (p.Asn665Ser)not specified [RCV004213099]uncertain significance149283560792835607Humanname
156345750CV2377742single nucleotide variantNM_005113.4(GOLGA5):c.1133G>A (p.Arg378His)not specified [RCV004230329]uncertain significance149281156792811567Humanname
329399024CV2428724single nucleotide variantNM_005113.4(GOLGA5):c.1046C>G (p.Thr349Ser)not specified [RCV004255514]uncertain significance149281030792810307Humanname
329394420CV2461341single nucleotide variantNM_005113.4(GOLGA5):c.1852C>A (p.Gln618Lys)not specified [RCV004267502]uncertain significance149283325492833254Humanname
329377294CV2462524single nucleotide variantNM_005113.4(GOLGA5):c.2086A>T (p.Ile696Leu)not specified [RCV004278482]uncertain significance149283742092837420Humanname
401719103CV2679417single nucleotide variantNM_005113.4(GOLGA5):c.1001A>G (p.Gln334Arg)not specified [RCV004285944]uncertain significance149281026292810262Humanname
401721930CV2680746single nucleotide variantNM_005113.4(GOLGA5):c.1769G>A (p.Arg590Gln)not specified [RCV004293399]uncertain significance149283317192833171Humanname
401718670CV2704736single nucleotide variantNM_005113.4(GOLGA5):c.1937A>G (p.Asn646Ser)not specified [RCV004307336]likely benign149283333992833339Humanname
401764796CV2705376single nucleotide variantNM_005113.4(GOLGA5):c.1355G>C (p.Gly452Ala)not specified [RCV004312048]uncertain significance149281628592816285Humanname
405769567CV3262294single nucleotide variantNM_005113.4(GOLGA5):c.1157G>A (p.Arg386His)not specified [RCV004395684]uncertain significance149281159192811591Humanname
405769573CV3262295single nucleotide variantNM_005113.4(GOLGA5):c.1183C>G (p.Leu395Val)not specified [RCV004395685]uncertain significance149281161792811617Humanname
405769579CV3262296single nucleotide variantNM_005113.4(GOLGA5):c.1291T>C (p.Tyr431His)not specified [RCV004395686]uncertain significance149281172592811725Humanname
405769586CV3262297single nucleotide variantNM_005113.4(GOLGA5):c.1439A>T (p.Glu480Val)not specified [RCV004395687]uncertain significance149281636992816369Humanname
405769592CV3262298single nucleotide variantNM_005113.4(GOLGA5):c.1460G>T (p.Gly487Val)not specified [RCV004395688]uncertain significance149281639092816390Humanname
405769596CV3262299single nucleotide variantNM_005113.4(GOLGA5):c.1483G>A (p.Glu495Lys)not specified [RCV004395689]uncertain significance149281641392816413Humanname
405769603CV3262300single nucleotide variantNM_005113.4(GOLGA5):c.1693G>A (p.Glu565Lys)not specified [RCV004395690]uncertain significance149282461892824618Humanname
405769609CV3262301single nucleotide variantNM_005113.4(GOLGA5):c.2158A>C (p.Thr720Pro)not specified [RCV004395691]uncertain significance149283940892839408Humanname
407520201CV3439746single nucleotide variantNM_005113.4(GOLGA5):c.1100G>A (p.Ser367Asn)not specified [RCV004629989]uncertain significance149281036192810361Humanname
407520204CV3439747single nucleotide variantNM_005113.4(GOLGA5):c.1723A>G (p.Thr575Ala)not specified [RCV004629990]uncertain significance149283312592833125Humanname
407520210CV3439749single nucleotide variantNM_005113.4(GOLGA5):c.1852C>G (p.Gln618Glu)not specified [RCV004629992]uncertain significance149283325492833254Humanname
407520214CV3439751single nucleotide variantNM_005113.4(GOLGA5):c.2173C>G (p.His725Asp)not specified [RCV004629994]uncertain significance149283942392839423Humanname
597788824CV3678452single nucleotide variantNM_005113.4(GOLGA5):c.1529C>T (p.Ala510Val)not specified [RCV004932819]uncertain significance149281974592819745Humanname
597788828CV3678454single nucleotide variantNM_005113.4(GOLGA5):c.1292A>G (p.Tyr431Cys)not specified [RCV004932820]uncertain significance149281172692811726Humanname
597731476CV3678455single nucleotide variantNM_005113.4(GOLGA5):c.2087T>A (p.Ile696Lys)not specified [RCV004919924]uncertain significance149283742192837421Humanname
597731496CV3678457single nucleotide variantNM_005113.4(GOLGA5):c.2153C>G (p.Thr718Ser)not specified [RCV004919926]uncertain significance149283940392839403Humanname
598264589CV3974503single nucleotide variantNM_005113.4(GOLGA5):c.1414C>T (p.Arg472Trp)not specified [RCV005348883]uncertain significance149281634492816344Humanname
598232931CV3974504single nucleotide variantNM_005113.4(GOLGA5):c.1561A>G (p.Ile521Val)not specified [RCV005342679]uncertain significance149281977792819777Humanname
598264593CV3974505single nucleotide variantNM_005113.4(GOLGA5):c.1610G>T (p.Arg537Leu)not specified [RCV005348884]uncertain significance149281982692819826Humanname
598264598CV3974507single nucleotide variantNM_005113.4(GOLGA5):c.1927G>A (p.Gly643Arg)not specified [RCV005348885]uncertain significance149283332992833329Humanname
15161025CV714276single nucleotide variantNM_005113.4(GOLGA5):c.1120G>A (p.Glu374Lys)not provided [RCV000970014]likely benign149281155492811554Humanname