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 All species
(View Results for all Objects and Ontologies)

42 records found for search term Mkrn1
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15127934CV782804single nucleotide variantNM_013446.4(MKRN1):c.90G>T (p.Pro30=)not provided [RCV000980626]likely benign7140479255140479255Humanname
155916426CV2336148single nucleotide variantNM_013446.4(MKRN1):c.59C>A (p.Ala20Glu)not specified [RCV004189741]uncertain significance7140479286140479286Humanname
155929960CV2361005single nucleotide variantNM_013446.4(MKRN1):c.94C>A (p.Pro32Thr)not specified [RCV004216201]uncertain significance7140479251140479251Humanname
401866155CV2775439single nucleotide variantNM_013446.4(MKRN1):c.80C>A (p.Ser27Tyr)not specified [RCV004348835]uncertain significance7140479265140479265Humanname
405671298CV3309048single nucleotide variantNM_013446.4(MKRN1):c.89C>G (p.Pro30Arg)not specified [RCV004441329]uncertain significance7140479256140479256Humanname
407486326CV3457244single nucleotide variantNM_013446.4(MKRN1):c.31G>T (p.Ala11Ser)not specified [RCV004640871]uncertain significance7140479314140479314Humanname
597636262CV3560715single nucleotide variantNM_013446.4(MKRN1):c.59C>G (p.Ala20Gly)not specified [RCV004824501]uncertain significance7140479286140479286Humanname
597640707CV3560718single nucleotide variantNM_013446.4(MKRN1):c.35C>G (p.Thr12Arg)not specified [RCV004825331]uncertain significance7140479310140479310Humanname
155914185CV2242638single nucleotide variantNM_013446.4(MKRN1):c.265G>C (p.Val89Leu)not specified [RCV004113694]uncertain significance7140471932140471932Humanname
155912862CV2245667single nucleotide variantNM_013446.4(MKRN1):c.217G>C (p.Asp73His)not specified [RCV004111551]uncertain significance7140471980140471980Humanname
405679121CV3318217single nucleotide variantNM_013446.4(MKRN1):c.280C>G (p.Gln94Glu)not specified [RCV004442868]uncertain significance7140471917140471917Humanname
597640672CV3560709single nucleotide variantNM_013446.4(MKRN1):c.254C>T (p.Pro85Leu)not specified [RCV004825325]uncertain significance7140471943140471943Humanname
597636267CV3560716single nucleotide variantNM_013446.4(MKRN1):c.139G>A (p.Gly47Ser)not specified [RCV004824502]uncertain significance7140479206140479206Humanname
598187435CV3989264single nucleotide variantNM_013446.4(MKRN1):c.133G>A (p.Gly45Ser)not specified [RCV005373561]uncertain significance7140479212140479212Humanname
156279671CV2252181single nucleotide variantNM_013446.4(MKRN1):c.380C>G (p.Ser127Cys)not specified [RCV004122194]uncertain significance7140459871140459871Humanname
156254591CV2284189single nucleotide variantNM_013446.4(MKRN1):c.758C>T (p.Ser253Leu)not specified [RCV004146563]uncertain significance7140459020140459020Humanname
156345381CV2291027single nucleotide variantNM_013446.4(MKRN1):c.575A>G (p.Gln192Arg)not specified [RCV004151567]uncertain significance7140459203140459203Humanname
155908714CV2307131single nucleotide variantNM_013446.4(MKRN1):c.530C>G (p.Pro177Arg)not specified [RCV004159611]uncertain significance7140459721140459721Humanname
156133288CV2350282single nucleotide variantNM_013446.4(MKRN1):c.440G>A (p.Gly147Asp)not specified [RCV004202237]uncertain significance7140459811140459811Humanname
329398954CV2428588single nucleotide variantNM_013446.4(MKRN1):c.437C>T (p.Thr146Ile)not specified [RCV004255398]uncertain significance7140459814140459814Humanname
405668243CV3308240single nucleotide variantNM_013446.4(MKRN1):c.442G>A (p.Glu148Lys)not specified [RCV004440712]uncertain significance7140459809140459809Humanname
405669830CV3308749single nucleotide variantNM_013446.4(MKRN1):c.866A>C (p.Tyr289Ser)not specified [RCV004441030]uncertain significance7140456772140456772Humanname
407486337CV3457246single nucleotide variantNM_013446.4(MKRN1):c.385G>A (p.Ala129Thr)not specified [RCV004640873]uncertain significance7140459866140459866Humanname
407486345CV3457247single nucleotide variantNM_013446.4(MKRN1):c.578G>C (p.Gly193Ala)not specified [RCV004640874]uncertain significance7140459200140459200Humanname
597640678CV3560710single nucleotide variantNM_013446.4(MKRN1):c.817G>A (p.Val273Met)not specified [RCV004825326]uncertain significance7140456821140456821Humanname
597640684CV3560711single nucleotide variantNM_013446.4(MKRN1):c.739A>G (p.Met247Val)not specified [RCV004825327]likely benign7140459039140459039Humanname
597640695CV3560713single nucleotide variantNM_013446.4(MKRN1):c.703T>C (p.Ser235Pro)not specified [RCV004825329]uncertain significance7140459075140459075Humanname
598187421CV3989261single nucleotide variantNM_013446.4(MKRN1):c.616G>A (p.Ala206Thr)not specified [RCV005373559]uncertain significance7140459162140459162Humanname
598166295CV3989265single nucleotide variantNM_013446.4(MKRN1):c.352A>G (p.Thr118Ala)not specified [RCV005369324]uncertain significance7140459899140459899Humanname
156396458CV2326284single nucleotide variantNM_013446.4(MKRN1):c.1130G>A (p.Arg377His)not specified [RCV004180530]uncertain significance7140455201140455201Humanname
329361340CV2436916single nucleotide variantNM_013446.4(MKRN1):c.1234C>T (p.Arg412Trp)not specified [RCV004260297]uncertain significance7140455097140455097Humanname
405795510CV3377383single nucleotide variantNM_013446.4(MKRN1):c.1186C>T (p.Arg396Cys)not specified [RCV004507395]uncertain significance7140455145140455145Humanname
405660940CV3379452single nucleotide variantNM_013446.4(MKRN1):c.1382C>T (p.Thr461Ile)not specified [RCV004512911]uncertain significance7140454584140454584Humanname
405653948CV3380062single nucleotide variantNM_013446.4(MKRN1):c.1286G>A (p.Ser429Asn)not specified [RCV004510502]uncertain significance7140454680140454680Humanname
407486331CV3457245single nucleotide variantNM_013446.4(MKRN1):c.1076T>A (p.Leu359Gln)not specified [RCV004640872]likely benign7140455811140455811Humanname
597640689CV3560712single nucleotide variantNM_013446.4(MKRN1):c.1398G>T (p.Glu466Asp)not specified [RCV004825328]uncertain significance7140454568140454568Humanname
597640701CV3560717single nucleotide variantNM_013446.4(MKRN1):c.1334G>A (p.Gly445Asp)not specified [RCV004825330]uncertain significance7140454632140454632Humanname
598166289CV3989262single nucleotide variantNM_013446.4(MKRN1):c.1381A>G (p.Thr461Ala)not specified [RCV005369323]uncertain significance7140454585140454585Humanname
598187428CV3989263single nucleotide variantNM_013446.4(MKRN1):c.1285A>G (p.Ser429Gly)not specified [RCV005373560]uncertain significance7140454681140454681Humanname
598187443CV3989266single nucleotide variantNM_013446.4(MKRN1):c.1277G>C (p.Arg426Thr)not specified [RCV005373562]uncertain significance7140454689140454689Humanname
598166301CV3989267single nucleotide variantNM_013446.4(MKRN1):c.1112G>C (p.Arg371Thr)not specified [RCV005369325]uncertain significance7140455219140455219Humanname
598166306CV3989268single nucleotide variantNM_013446.4(MKRN1):c.1341G>A (p.Met447Ile)not specified [RCV005369326]uncertain significance7140454625140454625Humanname