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Variants search result for Homo sapiens
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65 records found for search term Cyp2s1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156208917CV2382564single nucleotide variantNM_030622.8(CYP2S1):c.23C>T (p.Ala8Val)not specified [RCV004232892]uncertain significance194119328741193287Humanname
405667581CV3239732single nucleotide variantNM_030622.8(CYP2S1):c.13G>A (p.Gly5Ser)not specified [RCV004367976]uncertain significance194119327741193277Humanname
405667591CV3239734single nucleotide variantNM_030622.8(CYP2S1):c.178C>T (p.Leu60=)not specified [RCV004367978]likely benign194119454441194544Humanname
156244322CV2283338single nucleotide variantNM_030622.8(CYP2S1):c.71C>T (p.Ser24Phe)not specified [RCV004145995]uncertain significance194119333541193335Humanname
156178793CV2331340single nucleotide variantNM_030622.8(CYP2S1):c.55C>A (p.Leu19Met)not specified [RCV004183982]uncertain significance194119331941193319Humanname
401928834CV2808719single nucleotide variantNM_030622.8(CYP2S1):c.771G>C (p.Gly257=)not provided [RCV003406986]likely benign194119882541198825Humanname
407452537CV3420177single nucleotide variantNM_030622.8(CYP2S1):c.88G>T (p.Gly30Cys)not specified [RCV004608526]uncertain significance194119335241193352Humanname
15165227CV716459single nucleotide variantNM_030622.8(CYP2S1):c.423G>A (p.Gly141=)not provided [RCV000970905]benign194119785841197858Humanname
156043320CV2305795single nucleotide variantNM_030622.8(CYP2S1):c.226C>T (p.Arg76Trp)not specified [RCV004167600]uncertain significance194119459241194592Humanname
156226362CV2352734single nucleotide variantNM_030622.8(CYP2S1):c.199G>T (p.Val67Leu)not specified [RCV004198756]uncertain significance194119456541194565Humanname
401884375CV2765890single nucleotide variantNM_030622.8(CYP2S1):c.197C>T (p.Pro66Leu)not specified [RCV004337923]uncertain significance194119456341194563Humanname
401928836CV2808720single nucleotide variantNM_030622.8(CYP2S1):c.1407G>A (p.Pro469=)not provided [RCV003406987]likely benign194120638041206380Humanname
407452529CV3420172single nucleotide variantNM_030622.8(CYP2S1):c.281A>G (p.Gln94Arg)not specified [RCV004608521]uncertain significance194119464741194647Humanname
597672147CV3658298single nucleotide variantNM_030622.8(CYP2S1):c.227G>A (p.Arg76Gln)not specified [RCV004913322]uncertain significance194119459341194593Humanname
597672155CV3658299single nucleotide variantNM_030622.8(CYP2S1):c.193G>A (p.Gly65Arg)not specified [RCV004913323]uncertain significance194119455941194559Humanname
598238014CV3952513single nucleotide variantNM_030622.8(CYP2S1):c.137T>C (p.Leu46Pro)not specified [RCV005320747]uncertain significance194119340141193401Humanname
15191008CV728200single nucleotide variantNM_030622.8(CYP2S1):c.1059C>T (p.Thr353=)not provided [RCV000888259]benign194120353241203532Humanname
8636839CV92064single nucleotide variantNM_030622.7(CYP2S1):c.1365C>T (p.Thr455=)Malignant melanoma [RCV000072162]not provided194120633841206338Humanname
155910827CV2303687single nucleotide variantNM_030622.8(CYP2S1):c.523G>C (p.Ala175Pro)not specified [RCV004161758]uncertain significance194119849141198491Humanname
156299162CV2310699single nucleotide variantNM_030622.8(CYP2S1):c.409G>A (p.Asp137Asn)not specified [RCV004157353]uncertain significance194119784441197844Humanname
156170674CV2380617single nucleotide variantNM_030622.8(CYP2S1):c.298G>A (p.Gly100Ser)not specified [RCV004218207]uncertain significance194119466441194664Humanname
156264915CV2388999single nucleotide variantNM_030622.8(CYP2S1):c.934G>A (p.Gly312Ser)not specified [RCV004241994]uncertain significance194120133041201330Humanname
156040194CV2390418single nucleotide variantNM_030622.8(CYP2S1):c.428G>A (p.Arg143Gln)not provided [RCV004696274]|not specified [RCV004234116]uncertain significance194119786341197863Humanname
329377996CV2436103single nucleotide variantNM_030622.8(CYP2S1):c.775C>G (p.Leu259Val)not specified [RCV004249349]uncertain significance194119882941198829Humanname
329373636CV2452576single nucleotide variantNM_030622.8(CYP2S1):c.782C>T (p.Ala261Val)not specified [RCV004275160]uncertain significance194119883641198836Humanname
401779366CV2731763single nucleotide variantNM_030622.8(CYP2S1):c.302G>A (p.Arg101Gln)not specified [RCV004333021]uncertain significance194119466841194668Humanname
401876579CV2767640single nucleotide variantNM_030622.8(CYP2S1):c.947T>C (p.Leu316Pro)not specified [RCV004343782]uncertain significance194120134341201343Humanname
401863420CV2776895single nucleotide variantNM_030622.8(CYP2S1):c.470T>C (p.Val157Ala)not specified [RCV004351718]uncertain significance194119790541197905Humanname
401895323CV2786364single nucleotide variantNM_030622.8(CYP2S1):c.607C>T (p.Arg203Trp)not specified [RCV004361960]uncertain significance194119857541198575Humanname
405677663CV3239735single nucleotide variantNM_030622.8(CYP2S1):c.430G>C (p.Glu144Gln)not specified [RCV004370429]uncertain significance194119786541197865Humanname
405677666CV3239736single nucleotide variantNM_030622.8(CYP2S1):c.436G>A (p.Glu146Lys)not specified [RCV004370430]uncertain significance194119787141197871Humanname
405677676CV3239738single nucleotide variantNM_030622.8(CYP2S1):c.911C>T (p.Thr304Met)not specified [RCV004370432]uncertain significance194120130741201307Humanname
405677680CV3239739single nucleotide variantNM_030622.8(CYP2S1):c.988G>C (p.Glu330Gln)not specified [RCV004370433]uncertain significance194120346141203461Humanname
407452531CV3420173single nucleotide variantNM_030622.8(CYP2S1):c.790C>A (p.Pro264Thr)not specified [RCV004608522]uncertain significance194119884441198844Humanname
407452534CV3420174single nucleotide variantNM_030622.8(CYP2S1):c.749G>A (p.Arg250Gln)not specified [RCV004608523]likely benign194119880341198803Humanname
407452535CV3420175single nucleotide variantNM_030622.8(CYP2S1):c.709C>T (p.Leu237Phe)not specified [RCV004608524]uncertain significance194119876341198763Humanname
407452540CV3420178single nucleotide variantNM_030622.8(CYP2S1):c.508C>T (p.Pro170Ser)not specified [RCV004608527]uncertain significance194119847641198476Humanname
597672793CV3658290single nucleotide variantNM_030622.8(CYP2S1):c.620G>A (p.Gly207Asp)not specified [RCV004913314]uncertain significance194119858841198588Humanname
597672552CV3658291single nucleotide variantNM_030622.8(CYP2S1):c.797G>A (p.Arg266His)not specified [RCV004913315]uncertain significance194119885141198851Humanname
597672381CV3658293single nucleotide variantNM_030622.8(CYP2S1):c.977A>C (p.Lys326Thr)not specified [RCV004913317]uncertain significance194120345041203450Humanname
597672208CV3658295single nucleotide variantNM_030622.8(CYP2S1):c.568C>G (p.Arg190Gly)not specified [RCV004913319]uncertain significance194119853641198536Humanname
597672140CV3658297single nucleotide variantNM_030622.8(CYP2S1):c.578A>G (p.Tyr193Cys)not specified [RCV004913321]uncertain significance194119854641198546Humanname
597672163CV3658300single nucleotide variantNM_030622.8(CYP2S1):c.773A>C (p.Asn258Thr)not specified [RCV004913324]uncertain significance194119882741198827Humanname
598238023CV3952514single nucleotide variantNM_030622.8(CYP2S1):c.496C>T (p.Arg166Cys)not specified [RCV005320748]uncertain significance194119846441198464Humanname
598238028CV3952515single nucleotide variantNM_030622.8(CYP2S1):c.604G>A (p.Val202Ile)not specified [RCV005320749]uncertain significance194119857241198572Humanname
8628322CV83466single nucleotide variantNM_030622.7(CYP2S1):c.856G>A (p.Glu286Lys)Malignant melanoma [RCV000063547]not provided194120125241201252Humanname
156190690CV2206073single nucleotide variantNM_030622.8(CYP2S1):c.1313G>A (p.Arg438His)not specified [RCV004078484]uncertain significance194120628641206286Humanname
156171889CV2267785single nucleotide variantNM_030622.8(CYP2S1):c.1130G>A (p.Arg377Gln)not specified [RCV004134310]uncertain significance194120360341203603Humanname
156255171CV2311587single nucleotide variantNM_030622.8(CYP2S1):c.1223A>T (p.His408Leu)not specified [RCV004168400]uncertain significance194120601641206016Humanname
156173284CV2355155single nucleotide variantNM_030622.8(CYP2S1):c.1478G>A (p.Arg493His)not specified [RCV004198543]uncertain significance194120645141206451Humanname
156282222CV2363107single nucleotide variantNM_030622.8(CYP2S1):c.1467G>C (p.Gln489His)not specified [RCV004211232]uncertain significance194120644041206440Humanname
329392196CV2441303single nucleotide variantNM_030622.8(CYP2S1):c.1246C>T (p.Arg416Cys)not specified [RCV004257119]uncertain significance194120603941206039Humanname
329391554CV2452915single nucleotide variantNM_030622.8(CYP2S1):c.1453C>T (p.Pro485Ser)not specified [RCV004277554]uncertain significance194120642641206426Humanname
329377289CV2462520single nucleotide variantNM_030622.8(CYP2S1):c.1105A>G (p.Met369Val)not specified [RCV004276691]uncertain significance194120357841203578Humanname
405667566CV3239729single nucleotide variantNM_030622.8(CYP2S1):c.1036G>T (p.Asp346Tyr)not specified [RCV004367973]uncertain significance194120350941203509Humanname
405667571CV3239730single nucleotide variantNM_030622.8(CYP2S1):c.1135A>C (p.Thr379Pro)not specified [RCV004367974]uncertain significance194120360841203608Humanname
405667576CV3239731single nucleotide variantNM_030622.8(CYP2S1):c.1247G>A (p.Arg416His)not specified [RCV004367975]uncertain significance194120604041206040Humanname
405667584CV3239733single nucleotide variantNM_030622.8(CYP2S1):c.1478G>T (p.Arg493Leu)not specified [RCV004367977]uncertain significance194120645141206451Humanname
407452525CV3420170single nucleotide variantNM_030622.8(CYP2S1):c.1399T>C (p.Cys467Arg)not specified [RCV004608519]uncertain significance194120637241206372Humanname
407452527CV3420171single nucleotide variantNM_030622.8(CYP2S1):c.1406C>T (p.Pro469Leu)not specified [RCV004608520]likely benign194120637941206379Humanname
597672388CV3658292single nucleotide variantNM_030622.8(CYP2S1):c.1343C>T (p.Ala448Val)not specified [RCV004913316]uncertain significance194120631641206316Humanname
597672374CV3658294single nucleotide variantNM_030622.8(CYP2S1):c.1222C>T (p.His408Tyr)not specified [RCV004913318]uncertain significance194120601541206015Humanname
597672133CV3658296single nucleotide variantNM_030622.8(CYP2S1):c.1304T>C (p.Leu435Ser)not specified [RCV004913320]uncertain significance194120609741206097Humanname
598238003CV3952511single nucleotide variantNM_030622.8(CYP2S1):c.1046G>A (p.Arg349His)not specified [RCV005320745]uncertain significance194120351941203519Humanname
598238008CV3952512single nucleotide variantNM_030622.8(CYP2S1):c.1508C>G (p.Thr503Ser)not specified [RCV005320746]uncertain significance194120648141206481Humanname