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Variants search result for Homo sapiens
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68 records found for search term Cyp2a1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156015737CV2270004single nucleotide variantNM_000766.5(CYP2A13):c.46A>T (p.Thr16Ser)not specified [RCV004128992]uncertain significance194108851741088517Humanname
401737477CV2699827single nucleotide variantNM_000766.5(CYP2A13):c.92G>A (p.Gly31Glu)not specified [RCV004308472]uncertain significance194108856341088563Humanname
401910544CV2808718single nucleotide variantNM_000766.5(CYP2A13):c.688C>T (p.Leu230=)not provided [RCV003425188]likely benign194109176541091765Humanname
405667060CV3239624single nucleotide variantNM_000766.5(CYP2A13):c.95A>G (p.Lys32Arg)not specified [RCV004367868]uncertain significance194108856641088566Humanname
156171218CV2286629single nucleotide variantNM_000766.5(CYP2A13):c.176T>C (p.Met59Thr)not specified [RCV004142476]uncertain significance194108864741088647Humanname
156219791CV2393639single nucleotide variantNM_000766.5(CYP2A13):c.172C>T (p.Leu58Phe)not specified [RCV004231450]uncertain significance194108864341088643Humanname
329363370CV2465069single nucleotide variantNM_000766.5(CYP2A13):c.208A>G (p.Thr70Ala)not specified [RCV004286799]uncertain significance194108895641088956Humanname
401895895CV2775784single nucleotide variantNM_000766.5(CYP2A13):c.291G>T (p.Glu97Asp)not specified [RCV004344831]uncertain significance194108903941089039Humanname
405667006CV3239612single nucleotide variantNM_000766.5(CYP2A13):c.247G>A (p.Gly83Arg)not specified [RCV004367856]uncertain significance194108899541088995Humanname
597671386CV3658189single nucleotide variantNM_000766.5(CYP2A13):c.190C>A (p.Arg64Ser)not specified [RCV004913221]uncertain significance194108893841088938Humanname
598237574CV3952439single nucleotide variantNM_000766.5(CYP2A13):c.226C>T (p.Arg76Trp)not specified [RCV005320674]uncertain significance194108897441088974Humanname
156332558CV2220701single nucleotide variantNM_000766.5(CYP2A13):c.929T>C (p.Leu310Pro)not specified [RCV004097874]uncertain significance194109372741093727Humanname
156383416CV2223921single nucleotide variantNM_000766.5(CYP2A13):c.443G>A (p.Arg148His)not specified [RCV004093914]uncertain significance194109014641090146Humanname
155995105CV2250309single nucleotide variantNM_000766.5(CYP2A13):c.674C>T (p.Ser225Leu)not specified [RCV004127206]uncertain significance194109175141091751Humanname
156246097CV2263696single nucleotide variantNM_000766.5(CYP2A13):c.733G>A (p.Glu245Lys)not specified [RCV004135991]uncertain significance194109181041091810Humanname
156336814CV2270925single nucleotide variantNM_000766.5(CYP2A13):c.559T>C (p.Phe187Leu)not specified [RCV004131962]uncertain significance194109046941090469Humanname
155939999CV2294010single nucleotide variantNM_000766.5(CYP2A13):c.966G>T (p.Glu322Asp)not specified [RCV004149403]likely benign194109376441093764Humanname
156195677CV2318984single nucleotide variantNM_000766.5(CYP2A13):c.526C>A (p.Arg176Ser)not specified [RCV004178079]uncertain significance194109043641090436Humanname
156102122CV2367736single nucleotide variantNM_000766.5(CYP2A13):c.491A>G (p.His164Arg)not specified [RCV004213695]likely benign194109019441090194Humanname
156097651CV2375682single nucleotide variantNM_000766.5(CYP2A13):c.361G>C (p.Gly121Arg)not specified [RCV004226156]uncertain significance194109006441090064Humanname
156174769CV2377192single nucleotide variantNM_000766.5(CYP2A13):c.742A>G (p.Ile248Val)not specified [RCV004231867]uncertain significance194109181941091819Humanname
329360172CV2446624single nucleotide variantNM_000766.5(CYP2A13):c.398C>T (p.Ala133Val)not specified [RCV004251513]uncertain significance194109010141090101Humanname
329364095CV2469741single nucleotide variantNM_000766.5(CYP2A13):c.346G>T (p.Val116Leu)not specified [RCV004284936]uncertain significance194109004941090049Humanname
401723330CV2674915single nucleotide variantNM_000766.5(CYP2A13):c.445A>T (p.Ile149Phe)not specified [RCV004296228]uncertain significance194109014841090148Humanname
401731665CV2693930single nucleotide variantNM_000766.5(CYP2A13):c.539A>G (p.Asn180Ser)not specified [RCV004300227]uncertain significance194109044941090449Humanname
401855473CV2757400single nucleotide variantNM_000766.5(CYP2A13):c.806A>G (p.Asp269Gly)not specified [RCV004340800]uncertain significance194109188341091883Humanname
401884752CV2786566single nucleotide variantNM_000766.5(CYP2A13):c.931C>T (p.Arg311Cys)not specified [RCV004363712]uncertain significance194109372941093729Humanname
405667009CV3239613single nucleotide variantNM_000766.5(CYP2A13):c.394A>G (p.Ile132Val)not specified [RCV004367857]uncertain significance194109009741090097Humanname
405667015CV3239614single nucleotide variantNM_000766.5(CYP2A13):c.421G>A (p.Gly141Ser)not specified [RCV004367858]uncertain significance194109012441090124Humanname
405667019CV3239615single nucleotide variantNM_000766.5(CYP2A13):c.461G>A (p.Gly154Asp)not specified [RCV004367859]uncertain significance194109016441090164Humanname
405667026CV3239616single nucleotide variantNM_000766.5(CYP2A13):c.584A>G (p.Asp195Gly)not specified [RCV004367860]uncertain significance194109049441090494Humanname
405667030CV3239617single nucleotide variantNM_000766.5(CYP2A13):c.646A>G (p.Thr216Ala)not specified [RCV004367861]uncertain significance194109055641090556Humanname
405667034CV3239618single nucleotide variantNM_000766.5(CYP2A13):c.658T>C (p.Tyr220His)not specified [RCV004367862]uncertain significance194109173541091735Humanname
405667043CV3239620single nucleotide variantNM_000766.5(CYP2A13):c.785A>C (p.Asn262Thr)not specified [RCV004367864]uncertain significance194109186241091862Humanname
405667049CV3239621single nucleotide variantNM_000766.5(CYP2A13):c.794G>A (p.Arg265Gln)not specified [RCV004367865]uncertain significance194109187141091871Humanname
405667052CV3239622single nucleotide variantNM_000766.5(CYP2A13):c.821G>A (p.Arg274His)not specified [RCV004367866]uncertain significance194109189841091898Humanname
405667056CV3239623single nucleotide variantNM_000766.5(CYP2A13):c.947T>C (p.Leu316Pro)not specified [RCV004367867]uncertain significance194109374541093745Humanname
407452416CV3420108single nucleotide variantNM_000766.5(CYP2A13):c.916G>A (p.Val306Met)not specified [RCV004608457]uncertain significance194109371441093714Humanname
597671393CV3658190single nucleotide variantNM_000766.5(CYP2A13):c.407G>A (p.Arg136Lys)not specified [RCV004913222]uncertain significance194109011041090110Humanname
597671415CV3658193single nucleotide variantNM_000766.5(CYP2A13):c.937G>A (p.Gly313Ser)not specified [RCV004913225]uncertain significance194109373541093735Humanname
597671424CV3658194single nucleotide variantNM_000766.5(CYP2A13):c.313G>T (p.Ala105Ser)not specified [RCV004913226]uncertain significance194108906141089061Humanname
598237561CV3952436single nucleotide variantNM_000766.5(CYP2A13):c.298G>A (p.Gly100Arg)not specified [RCV005320671]uncertain significance194108904641089046Humanname
598237564CV3952437single nucleotide variantNM_000766.5(CYP2A13):c.499A>C (p.Asn167His)not specified [RCV005320672]uncertain significance194109040941090409Humanname
598237580CV3952440single nucleotide variantNM_000766.5(CYP2A13):c.425A>G (p.Lys142Arg)not specified [RCV005320675]uncertain significance194109012841090128Humanname
155922523CV2218963single nucleotide variantNM_000766.5(CYP2A13):c.1006G>A (p.Gly336Ser)not specified [RCV004087145]uncertain significance194109427741094277Humanname
155901300CV2241971single nucleotide variantNM_000766.5(CYP2A13):c.1342G>A (p.Glu448Lys)not specified [RCV004108922]uncertain significance194109579841095798Humanname
156243967CV2267308single nucleotide variantNM_000766.5(CYP2A13):c.1344G>T (p.Glu448Asp)not specified [RCV004133979]uncertain significance194109580041095800Humanname
155996050CV2277363single nucleotide variantNM_000766.5(CYP2A13):c.1442C>G (p.Ala481Gly)not specified [RCV004144785]uncertain significance194109589841095898Humanname
156156452CV2393486single nucleotide variantNM_000766.5(CYP2A13):c.1354T>G (p.Phe452Val)not specified [RCV004228975]uncertain significance194109581041095810Humanname
156320172CV2400312single nucleotide variantNM_000766.5(CYP2A13):c.1085T>C (p.Phe362Ser)not provided [RCV004696307]|not specified [RCV004244371]uncertain significance194109435641094356Humanname
155969870CV2400809single nucleotide variantNM_000766.5(CYP2A13):c.1379T>G (p.Phe460Cys)not specified [RCV004242468]uncertain significance194109583541095835Humanname
401752743CV2682922single nucleotide variantNM_000766.5(CYP2A13):c.1255A>G (p.Lys419Glu)not specified [RCV004283716]likely benign194109505241095052Humanname
401729300CV2690132single nucleotide variantNM_000766.5(CYP2A13):c.1291C>T (p.Pro431Ser)not specified [RCV004300362]uncertain significance194109508841095088Humanname
401893445CV2763415single nucleotide variantNM_000766.5(CYP2A13):c.1166C>T (p.Thr389Ile)not specified [RCV004349304]uncertain significance194109496341094963Humanname
401886771CV2776733single nucleotide variantNM_000766.5(CYP2A13):c.1322G>C (p.Gly441Ala)not specified [RCV004357889]uncertain significance194109577841095778Humanname
405666987CV3239608single nucleotide variantNM_000766.5(CYP2A13):c.1061C>G (p.Ala354Gly)not specified [RCV004367852]uncertain significance194109433241094332Humanname
405666992CV3239609single nucleotide variantNM_000766.5(CYP2A13):c.1142G>A (p.Arg381Gln)not specified [RCV004367853]uncertain significance194109441341094413Humanname
405666997CV3239610single nucleotide variantNM_000766.5(CYP2A13):c.1209G>C (p.Arg403Ser)not specified [RCV004367854]uncertain significance194109500641095006Humanname
405667002CV3239611single nucleotide variantNM_000766.5(CYP2A13):c.1223C>T (p.Pro408Leu)not specified [RCV004367855]uncertain significance194109502041095020Humanname
407452413CV3420107single nucleotide variantNM_000766.5(CYP2A13):c.1225C>T (p.Arg409Trp)not specified [RCV004608456]uncertain significance194109502241095022Humanname
407452418CV3420109single nucleotide variantNM_000766.5(CYP2A13):c.1316G>A (p.Cys439Tyr)not specified [RCV004608458]uncertain significance194109577241095772Humanname
597671406CV3658192single nucleotide variantNM_000766.5(CYP2A13):c.1205C>T (p.Pro402Leu)not specified [RCV004913224]uncertain significance194109500241095002Humanname
597671431CV3658195single nucleotide variantNM_000766.5(CYP2A13):c.1260G>C (p.Lys420Asn)not specified [RCV004913227]uncertain significance194109505741095057Humanname
597671441CV3658196single nucleotide variantNM_000766.5(CYP2A13):c.1424C>T (p.Pro475Leu)not specified [RCV004913228]uncertain significance194109588041095880Humanname
597671657CV3658197single nucleotide variantNM_000766.5(CYP2A13):c.1048C>A (p.Pro350Thr)not specified [RCV004913229]uncertain significance194109431941094319Humanname
597671664CV3658198single nucleotide variantNM_000766.5(CYP2A13):c.1364C>T (p.Thr455Ile)not specified [RCV004913230]uncertain significance194109582041095820Humanname
598237569CV3952438single nucleotide variantNM_000766.5(CYP2A13):c.1382G>A (p.Arg461His)not specified [RCV005320673]uncertain significance194109583841095838Humanname
8636838CV92063single nucleotide variantNM_000766.4(CYP2A13):c.1454G>A (p.Arg485Gln)Malignant melanoma [RCV000072161]not provided194109591041095910Humanname