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54 records found for search term Cyp4a2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8629576CV84723single nucleotide variantNM_001010969.3(CYP4A22):c.1364+3G>AMalignant melanoma [RCV000064805]not provided14714615647146156Humanname
405678449CV3239814single nucleotide variantNM_001010969.4(CYP4A22):c.53T>C (p.Ile18Thr)not specified [RCV004370508]uncertain significance14713753847137538Humanname
407477522CV3420213single nucleotide variantNM_001010969.4(CYP4A22):c.32G>A (p.Arg11His)not specified [RCV004608562]uncertain significance14713751747137517Humanname
407477529CV3420214single nucleotide variantNM_001010969.4(CYP4A22):c.49G>A (p.Gly17Arg)not specified [RCV004608563]uncertain significance14713753447137534Humanname
8625012CV80131single nucleotide variantNM_001010969.3(CYP4A22):c.597G>A (p.Lys199=)Malignant melanoma [RCV000060207]not provided14714335547143355Humanname
8625013CV80132single nucleotide variantNM_001010969.3(CYP4A22):c.987G>A (p.Gly329=)Malignant melanoma [RCV000060208]not provided14714463947144639Humanname
401743978CV2688071single nucleotide variantNM_001010969.4(CYP4A22):c.140C>G (p.Ala47Gly)not specified [RCV004305134]uncertain significance14713762547137625Humanname
401899741CV2762104single nucleotide variantNM_001010969.4(CYP4A22):c.196T>C (p.Phe66Leu)not specified [RCV004341920]uncertain significance14714078047140780Humanname
401862451CV2762105single nucleotide variantNM_001010969.4(CYP4A22):c.204C>G (p.His68Gln)not specified [RCV004341921]likely benign14714078847140788Humanname
597672409CV3654855single nucleotide variantNM_001010969.4(CYP4A22):c.133C>A (p.Leu45Ile)not specified [RCV004913373]uncertain significance14713761847137618Humanname
597672429CV3654858single nucleotide variantNM_001010969.4(CYP4A22):c.140C>A (p.Ala47Asp)not specified [RCV004913376]uncertain significance14713762547137625Humanname
598249782CV3952570single nucleotide variantNM_001010969.4(CYP4A22):c.287G>A (p.Arg96His)not specified [RCV005322794]uncertain significance14714087147140871Humanname
156185619CV1686047single nucleotide variantNM_001010969.4(CYP4A22):c.691T>C (p.Cys231Arg)Pulmonary disease, chronic obstructive, susceptibility to [RCV002508847]association14714381747143817Human1name
155966423CV2216667single nucleotide variantNM_001010969.4(CYP4A22):c.851A>T (p.Lys284Met)not specified [RCV004083123]uncertain significance14714441747144417Humanname
155965547CV2261807single nucleotide variantNM_001010969.4(CYP4A22):c.583G>A (p.Asp195Asn)not specified [RCV004126084]uncertain significance14714334147143341Humanname
156135983CV2284778single nucleotide variantNM_001010969.4(CYP4A22):c.831G>T (p.Glu277Asp)not specified [RCV004142959]uncertain significance14714439747144397Humanname
156285471CV2345580single nucleotide variantNM_001010969.4(CYP4A22):c.706T>G (p.Phe236Val)not specified [RCV004205534]uncertain significance14714383247143832Humanname
329369860CV2424962single nucleotide variantNM_001010969.4(CYP4A22):c.990C>G (p.Ile330Met)not specified [RCV004250628]uncertain significance14714464247144642Humanname
401737997CV2676093single nucleotide variantNM_001010969.4(CYP4A22):c.500G>A (p.Arg167Gln)not specified [RCV004284319]uncertain significance14714222547142225Humanname
401735314CV2706748single nucleotide variantNM_001010969.4(CYP4A22):c.299A>G (p.Tyr100Cys)not specified [RCV004319309]uncertain significance14714088347140883Humanname
401781560CV2731681single nucleotide variantNM_001010969.4(CYP4A22):c.731G>A (p.Ser244Asn)not specified [RCV004331785]uncertain significance14714385747143857Humanname
401892077CV2775921single nucleotide variantNM_001010969.4(CYP4A22):c.761G>A (p.Arg254His)not specified [RCV004344947]uncertain significance14714388747143887Humanname
405678453CV3239813single nucleotide variantNM_001010969.4(CYP4A22):c.486G>A (p.Met162Ile)not specified [RCV004370507]uncertain significance14714221147142211Humanname
405678446CV3239815single nucleotide variantNM_001010969.4(CYP4A22):c.600T>G (p.Ser200Arg)not specified [RCV004370509]uncertain significance14714335847143358Humanname
405678440CV3239816single nucleotide variantNM_001010969.4(CYP4A22):c.725T>A (p.Ile242Asn)not specified [RCV004370510]uncertain significance14714385147143851Humanname
405678437CV3239817single nucleotide variantNM_001010969.4(CYP4A22):c.763G>A (p.Ala255Thr)not specified [RCV004370511]uncertain significance14714388947143889Humanname
405678430CV3239818single nucleotide variantNM_001010969.4(CYP4A22):c.788C>T (p.Thr263Ile)not specified [RCV004370512]uncertain significance14714391447143914Humanname
405678429CV3239819single nucleotide variantNM_001010969.4(CYP4A22):c.841G>A (p.Glu281Lys)not specified [RCV004370513]uncertain significance14714440747144407Humanname
597672443CV3654860single nucleotide variantNM_001010969.4(CYP4A22):c.722C>A (p.Thr241Asn)not specified [RCV004913378]uncertain significance14714384847143848Humanname
598249767CV3952568single nucleotide variantNM_001010969.4(CYP4A22):c.565G>A (p.Val189Ile)not specified [RCV005322792]likely benign14714332347143323Humanname
155962479CV2285661single nucleotide variantNM_001010969.4(CYP4A22):c.1483G>C (p.Val495Leu)not specified [RCV004141519]uncertain significance14714872047148720Humanname
156250268CV2286695single nucleotide variantNM_001010969.4(CYP4A22):c.1337C>T (p.Ala446Val)not specified [RCV004142522]uncertain significance14714612647146126Humanname
155904322CV2298783single nucleotide variantNM_001010969.4(CYP4A22):c.1183A>G (p.Thr395Ala)not specified [RCV004156340]uncertain significance14714493147144931Humanname
156226372CV2352735single nucleotide variantNM_001010969.4(CYP4A22):c.1205G>C (p.Gly402Ala)not specified [RCV004198757]uncertain significance14714495347144953Humanname
329382146CV2467525single nucleotide variantNM_001010969.4(CYP4A22):c.1270G>T (p.Val424Leu)not specified [RCV004287126]uncertain significance14714591347145913Humanname
401730315CV2680097single nucleotide variantNM_001010969.4(CYP4A22):c.1162G>A (p.Gly388Ser)not specified [RCV004286588]uncertain significance14714491047144910Humanname
401765792CV2683426single nucleotide variantNM_001010969.4(CYP4A22):c.1375G>A (p.Gly459Arg)not specified [RCV004288193]uncertain significance14714861247148612Humanname
401759671CV2698586single nucleotide variantNM_001010969.4(CYP4A22):c.1471A>G (p.Met491Val)not specified [RCV004299071]uncertain significance14714870847148708Humanname
401752750CV2707113single nucleotide variantNM_001010969.4(CYP4A22):c.1028A>T (p.His343Leu)not specified [RCV004321693]uncertain significance14714468047144680Humanname
401763920CV2725359single nucleotide variantNM_001010969.4(CYP4A22):c.1289T>G (p.Val430Gly)not specified [RCV004320011]uncertain significance14714607847146078Humanname
405678474CV3239807single nucleotide variantNM_001010969.4(CYP4A22):c.1001T>C (p.Leu334Pro)not specified [RCV004370501]uncertain significance14714465347144653Humanname
405678471CV3239808single nucleotide variantNM_001010969.4(CYP4A22):c.1082T>C (p.Ile361Thr)not specified [RCV004370502]uncertain significance14714473447144734Humanname
405678468CV3239809single nucleotide variantNM_001010969.4(CYP4A22):c.1134G>C (p.Glu378Asp)not specified [RCV004370503]uncertain significance14714488247144882Humanname
405678464CV3239810single nucleotide variantNM_001010969.4(CYP4A22):c.1263C>A (p.Asn421Lys)not specified [RCV004370504]uncertain significance14714590647145906Humanname
405678460CV3239811single nucleotide variantNM_001010969.4(CYP4A22):c.1415C>G (p.Ala472Gly)not specified [RCV004370505]uncertain significance14714865247148652Humanname
405678457CV3239812single nucleotide variantNM_001010969.4(CYP4A22):c.1549G>A (p.Asp517Asn)not specified [RCV004370506]uncertain significance14714878647148786Humanname
407477516CV3420212single nucleotide variantNM_001010969.4(CYP4A22):c.1513C>T (p.Arg505Cys)not specified [RCV004608561]uncertain significance14714875047148750Humanname
597672417CV3654856single nucleotide variantNM_001010969.4(CYP4A22):c.1280A>G (p.Asn427Ser)not specified [RCV004913374]uncertain significance14714592347145923Humanname
597672423CV3654857single nucleotide variantNM_001010969.4(CYP4A22):c.1412G>C (p.Arg471Thr)not specified [RCV004913375]likely benign14714864947148649Humanname
597672435CV3654859single nucleotide variantNM_001010969.4(CYP4A22):c.1276C>G (p.Pro426Ala)not specified [RCV004913377]uncertain significance14714591947145919Humanname
597672451CV3654861single nucleotide variantNM_001010969.4(CYP4A22):c.1535C>T (p.Pro512Leu)not specified [RCV004913379]uncertain significance14714877247148772Humanname
598249774CV3952569single nucleotide variantNM_001010969.4(CYP4A22):c.1043G>A (p.Arg348Gln)not specified [RCV005322793]uncertain significance14714469547144695Humanname
8629574CV84721single nucleotide variantNM_001010969.3(CYP4A22):c.1357G>A (p.Gly453Arg)Malignant melanoma [RCV000064803]not provided14714614647146146Humanname
8629575CV84722single nucleotide variantNM_001010969.3(CYP4A22):c.1358G>A (p.Gly453Glu)Malignant melanoma [RCV000064804]not provided14714614747146147Humanname