Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Behavioral & Substance Use Disorder Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Advanced Search (OLGA)
Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)

48 records found for search term Cyb5r4
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8582233CV116702single nucleotide variantNM_016230.3(CYB5R4):c.229+8943A>TLung cancer [RCV000097225]uncertain significance68387327183873271Humanname
156026606CV2242372single nucleotide variantNM_016230.4(CYB5R4):c.62G>C (p.Gly21Ala)not specified [RCV004111376]uncertain significance68385984483859844Humanname
156030696CV2278737single nucleotide variantNM_016230.4(CYB5R4):c.37A>G (p.Arg13Gly)not specified [RCV004134928]uncertain significance68385981983859819Humanname
597655828CV3657997single nucleotide variantNM_016230.4(CYB5R4):c.28C>T (p.Pro10Ser)not specified [RCV004911120]uncertain significance68385981083859810Humanname
598236979CV3956253single nucleotide variantNM_016230.4(CYB5R4):c.49C>T (p.Arg17Cys)not specified [RCV005320550]uncertain significance68385983183859831Humanname
401758741CV2694254single nucleotide variantNM_016230.4(CYB5R4):c.146G>A (p.Gly49Glu)not specified [RCV004302666]uncertain significance68386424583864245Humanname
401719017CV2731106single nucleotide variantNM_016230.4(CYB5R4):c.281A>G (p.Asp94Gly)not specified [RCV004332649]uncertain significance68389357383893573Humanname
597655812CV3657995single nucleotide variantNM_016230.4(CYB5R4):c.172A>G (p.Thr58Ala)not specified [RCV004911118]uncertain significance68386427183864271Humanname
597655836CV3657998single nucleotide variantNM_016230.4(CYB5R4):c.200A>G (p.Lys67Arg)not specified [RCV004911121]uncertain significance68386429983864299Humanname
8632187CV87393single nucleotide variantNM_016230.3(CYB5R4):c.265C>T (p.His89Tyr)Malignant melanoma [RCV000067484]not provided68389355783893557Humanname
156358187CV2250938single nucleotide variantNM_016230.4(CYB5R4):c.331G>T (p.Val111Phe)not specified [RCV004123518]uncertain significance68390900983909009Humanname
156155820CV2266168single nucleotide variantNM_016230.4(CYB5R4):c.740A>C (p.Lys247Thr)not specified [RCV004128749]uncertain significance68392451883924518Humanname
156339862CV2268023single nucleotide variantNM_016230.4(CYB5R4):c.566A>G (p.Asp189Gly)not specified [RCV004136578]uncertain significance68392108383921083Humanname
155990846CV2276515single nucleotide variantNM_016230.4(CYB5R4):c.634G>A (p.Asp212Asn)not specified [RCV004144228]uncertain significance68392115183921151Humanname
156005383CV2290327single nucleotide variantNM_016230.4(CYB5R4):c.697G>T (p.Val233Phe)not specified [RCV004154761]uncertain significance68392447583924475Humanname
156009617CV2362020single nucleotide variantNM_016230.4(CYB5R4):c.869C>T (p.Thr290Met)not specified [RCV004209834]uncertain significance68393464983934649Humanname
401740721CV2680463single nucleotide variantNM_016230.4(CYB5R4):c.931G>A (p.Val311Ile)not specified [RCV004291107]uncertain significance68393471183934711Humanname
401782947CV2707625single nucleotide variantNM_016230.4(CYB5R4):c.710T>C (p.Val237Ala)not specified [RCV004306565]uncertain significance68392448883924488Humanname
401778005CV2718421single nucleotide variantNM_016230.4(CYB5R4):c.583A>G (p.Ile195Val)not specified [RCV004318241]likely benign68392110083921100Humanname
401776581CV2724755single nucleotide variantNM_016230.4(CYB5R4):c.589G>A (p.Val197Ile)not specified [RCV004332293]uncertain significance68392110683921106Humanname
405666111CV3239434single nucleotide variantNM_016230.4(CYB5R4):c.337C>T (p.Arg113Cys)not specified [RCV004367678]uncertain significance68390901583909015Humanname
405666115CV3239435single nucleotide variantNM_016230.4(CYB5R4):c.358A>G (p.Met120Val)not specified [RCV004367679]uncertain significance68390903683909036Humanname
405666120CV3239436single nucleotide variantNM_016230.4(CYB5R4):c.374T>A (p.Leu125Gln)not specified [RCV004367680]uncertain significance68390905283909052Humanname
405666131CV3239438single nucleotide variantNM_016230.4(CYB5R4):c.572A>G (p.Asn191Ser)not specified [RCV004367682]uncertain significance68392108983921089Humanname
405666138CV3239439single nucleotide variantNM_016230.4(CYB5R4):c.575T>C (p.Leu192Ser)not specified [RCV004367683]uncertain significance68392109283921092Humanname
405666143CV3239440single nucleotide variantNM_016230.4(CYB5R4):c.794T>C (p.Leu265Pro)not specified [RCV004367684]uncertain significance68392457283924572Humanname
405666146CV3239441single nucleotide variantNM_016230.4(CYB5R4):c.992G>A (p.Gly331Asp)not specified [RCV004367685]likely benign68393626083936260Humanname
597655787CV3657992single nucleotide variantNM_016230.4(CYB5R4):c.449T>C (p.Met150Thr)not specified [RCV004911115]uncertain significance68391800883918008Humanname
597655866CV3658001single nucleotide variantNM_016230.4(CYB5R4):c.617C>A (p.Ala206Glu)not specified [RCV004911124]uncertain significance68392113483921134Humanname
597655891CV3658004single nucleotide variantNM_016230.4(CYB5R4):c.568A>G (p.Ile190Val)not specified [RCV004911127]uncertain significance68392108583921085Humanname
597655901CV3658005single nucleotide variantNM_016230.4(CYB5R4):c.949A>G (p.Ile317Val)not specified [RCV004911128]uncertain significance68393472983934729Humanname
597655910CV3658006single nucleotide variantNM_016230.4(CYB5R4):c.710T>G (p.Val237Gly)not specified [RCV004911129]uncertain significance68392448883924488Humanname
598236973CV3956252single nucleotide variantNM_016230.4(CYB5R4):c.338G>A (p.Arg113His)not specified [RCV005320549]uncertain significance68390901683909016Humanname
598236984CV3956254single nucleotide variantNM_016230.4(CYB5R4):c.416A>G (p.Tyr139Cys)not specified [RCV005320551]uncertain significance68391441983914419Humanname
15164934CV710628single nucleotide variantNM_016230.4(CYB5R4):c.799C>G (p.Pro267Ala)not provided [RCV000970839]benign68392457783924577Humanname
156288047CV2327376single nucleotide variantNM_016230.4(CYB5R4):c.1412C>T (p.Ser471Leu)not specified [RCV004174803]uncertain significance68395536383955363Humanname
329391728CV2453071single nucleotide variantNM_016230.4(CYB5R4):c.1163A>G (p.Gln388Arg)not specified [RCV004277680]uncertain significance68394011083940110Humanname
401862585CV2775261single nucleotide variantNM_016230.4(CYB5R4):c.1283A>G (p.Asn428Ser)not specified [RCV004348384]uncertain significance68394053883940538Humanname
405666106CV3239433single nucleotide variantNM_016230.4(CYB5R4):c.1317A>C (p.Gln439His)not specified [RCV004367677]uncertain significance68394057283940572Humanname
597655798CV3657993single nucleotide variantNM_016230.4(CYB5R4):c.1393G>A (p.Gly465Ser)not specified [RCV004911116]uncertain significance68395534483955344Humanname
597655804CV3657994single nucleotide variantNM_016230.4(CYB5R4):c.1523A>G (p.Asp508Gly)not specified [RCV004911117]uncertain significance68395983583959835Humanname
597655819CV3657996single nucleotide variantNM_016230.4(CYB5R4):c.1156A>G (p.Lys386Glu)not specified [RCV004911119]uncertain significance68394010383940103Humanname
597655856CV3658000single nucleotide variantNM_016230.4(CYB5R4):c.1505G>C (p.Gly502Ala)not specified [RCV004911123]uncertain significance68395545683955456Humanname
597655875CV3658002single nucleotide variantNM_016230.4(CYB5R4):c.1546A>T (p.Ile516Phe)not specified [RCV004911125]uncertain significance68395985883959858Humanname
597655883CV3658003single nucleotide variantNM_016230.4(CYB5R4):c.1433T>C (p.Phe478Ser)not specified [RCV004911126]uncertain significance68395538483955384Humanname
598236969CV3956251single nucleotide variantNM_016230.4(CYB5R4):c.1018C>A (p.Pro340Thr)not specified [RCV005320548]uncertain significance68393628683936286Humanname
598236988CV3956255single nucleotide variantNM_016230.4(CYB5R4):c.1104G>C (p.Gln368His)not specified [RCV005320552]uncertain significance68393637283936372Humanname
152034503CV1669525deletionNM_016230.4(CYB5R4):c.1258_1259del (p.Arg420fs)not provided [RCV002223516]uncertain significance68394020583940206Humanname