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)

43 records found for search term Hoxd12
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597772866CV3679760single nucleotide variantNM_021193.4(HOXD12):c.8A>G (p.Glu3Gly)not specified [RCV004928772]uncertain significance2176099809176099809Humanname
598192209CV3971811single nucleotide variantNM_021193.4(HOXD12):c.4T>C (p.Cys2Arg)not specified [RCV005354406]uncertain significance2176099805176099805Humanname
405798290CV3263469single nucleotide variantNM_021193.4(HOXD12):c.61C>T (p.Pro21Ser)not specified [RCV004402108]uncertain significance2176099862176099862Humanname
597772876CV3679762single nucleotide variantNM_021193.4(HOXD12):c.62C>T (p.Pro21Leu)not specified [RCV004928774]uncertain significance2176099863176099863Humanname
156089612CV2295607single nucleotide variantNM_021193.4(HOXD12):c.160A>G (p.Thr54Ala)not specified [RCV004160692]uncertain significance2176099961176099961Humanname
401867801CV2777368single nucleotide variantNM_021193.4(HOXD12):c.176C>T (p.Ala59Val)not specified [RCV004354376]uncertain significance2176099977176099977Humanname
405289778CV3219667single nucleotide variantNM_021193.4(HOXD12):c.223C>A (p.Pro75Thr)HOXD12-related disorder [RCV003961958]likely benign2176100024176100024Humanname , trait , alternate_id
407528141CV3433842single nucleotide variantNM_021193.4(HOXD12):c.191C>A (p.Ala64Glu)not specified [RCV004633042]uncertain significance2176099992176099992Humanname
597772881CV3679763single nucleotide variantNM_021193.4(HOXD12):c.197C>T (p.Ala66Val)not specified [RCV004928775]uncertain significance2176099998176099998Humanname
598192216CV3971812single nucleotide variantNM_021193.4(HOXD12):c.251G>A (p.Gly84Asp)not specified [RCV005354407]uncertain significance2176100052176100052Humanname
156167345CV2200998single nucleotide variantNM_021193.4(HOXD12):c.681C>G (p.Ile227Met)not specified [RCV004074763]uncertain significance2176100628176100628Humanname
155914872CV2203855single nucleotide variantNM_021193.4(HOXD12):c.304G>C (p.Ala102Pro)HOXD12-related disorder [RCV004758914]|not specified [RCV004069916]uncertain significance2176100105176100105Humanname , trait , alternate_id
156337147CV2228645single nucleotide variantNM_021193.4(HOXD12):c.440C>T (p.Pro147Leu)not specified [RCV004092869]uncertain significance2176100241176100241Humanname
156074983CV2230102single nucleotide variantNM_021193.4(HOXD12):c.340C>A (p.Arg114Ser)not specified [RCV004099754]uncertain significance2176100141176100141Humanname
156151897CV2245238single nucleotide variantNM_021193.4(HOXD12):c.589G>A (p.Ala197Thr)not specified [RCV004107009]uncertain significance2176100536176100536Humanname
155976705CV2246053single nucleotide variantNM_021193.4(HOXD12):c.729C>A (p.Asp243Glu)not specified [RCV004113966]uncertain significance2176100676176100676Humanname
155957115CV2282016single nucleotide variantNM_021193.4(HOXD12):c.667G>T (p.Val223Phe)not specified [RCV004138773]uncertain significance2176100614176100614Humanname
156192328CV2289414single nucleotide variantNM_021193.4(HOXD12):c.513C>A (p.Asn171Lys)not specified [RCV004152370]uncertain significance2176100314176100314Humanname
156018037CV2302714single nucleotide variantNM_021193.4(HOXD12):c.431G>A (p.Arg144His)not specified [RCV004162646]uncertain significance2176100232176100232Humanname
156272289CV2315912single nucleotide variantNM_021193.4(HOXD12):c.726C>A (p.Ser242Arg)not specified [RCV004171680]uncertain significance2176100673176100673Humanname
156164607CV2319720single nucleotide variantNM_021193.4(HOXD12):c.497C>A (p.Thr166Asn)not specified [RCV004187257]uncertain significance2176100298176100298Humanname
155907924CV2354525single nucleotide variantNM_021193.4(HOXD12):c.706T>A (p.Ser236Thr)not specified [RCV004202506]uncertain significance2176100653176100653Humanname
156140862CV2358361single nucleotide variantNM_021193.4(HOXD12):c.713G>A (p.Arg238Lys)not specified [RCV004214171]uncertain significance2176100660176100660Humanname
156348272CV2375684single nucleotide variantNM_021193.4(HOXD12):c.695G>T (p.Arg232Leu)not specified [RCV004226158]uncertain significance2176100642176100642Humanname
329380069CV2466409single nucleotide variantNM_021193.4(HOXD12):c.797C>T (p.Ala266Val)not specified [RCV004273968]uncertain significance2176100744176100744Humanname
401741841CV2676538single nucleotide variantNM_021193.4(HOXD12):c.784C>G (p.Leu262Val)not specified [RCV004288728]uncertain significance2176100731176100731Humanname
401741122CV2680334single nucleotide variantNM_021193.4(HOXD12):c.463G>T (p.Gly155Trp)not specified [RCV004288587]uncertain significance2176100264176100264Humanname
401890174CV2763670single nucleotide variantNM_021193.4(HOXD12):c.415T>C (p.Tyr139His)not specified [RCV004343173]uncertain significance2176100216176100216Humanname
405797971CV3263468single nucleotide variantNM_021193.4(HOXD12):c.329A>C (p.Glu110Ala)not specified [RCV004402107]uncertain significance2176100130176100130Humanname
405797976CV3263470single nucleotide variantNM_021193.4(HOXD12):c.625T>C (p.Tyr209His)not specified [RCV004402109]uncertain significance2176100572176100572Humanname
407528132CV3433839single nucleotide variantNM_021193.4(HOXD12):c.761G>A (p.Arg254His)not specified [RCV004633039]uncertain significance2176100708176100708Humanname
407528135CV3433840single nucleotide variantNM_021193.4(HOXD12):c.347G>T (p.Arg116Leu)not specified [RCV004633040]uncertain significance2176100148176100148Humanname
407528138CV3433841single nucleotide variantNM_021193.4(HOXD12):c.587G>C (p.Gly196Ala)not specified [RCV004633041]uncertain significance2176100534176100534Humanname
407528144CV3433843single nucleotide variantNM_021193.4(HOXD12):c.499A>G (p.Lys167Glu)not specified [RCV004633043]uncertain significance2176100300176100300Humanname
597772844CV3679756single nucleotide variantNM_021193.4(HOXD12):c.743T>C (p.Ile248Thr)not specified [RCV004928768]uncertain significance2176100690176100690Humanname
597772849CV3679757single nucleotide variantNM_021193.4(HOXD12):c.616C>G (p.Arg206Gly)not specified [RCV004928769]uncertain significance2176100563176100563Humanname
597772855CV3679758single nucleotide variantNM_021193.4(HOXD12):c.652G>C (p.Glu218Gln)not specified [RCV004928770]uncertain significance2176100599176100599Humanname
597772860CV3679759single nucleotide variantNM_021193.4(HOXD12):c.335G>A (p.Arg112His)not specified [RCV004928771]uncertain significance2176100136176100136Humanname
597772887CV3679764single nucleotide variantNM_021193.4(HOXD12):c.458T>C (p.Leu153Pro)not specified [RCV004928776]uncertain significance2176100259176100259Humanname
598192172CV3971807single nucleotide variantNM_021193.4(HOXD12):c.482G>A (p.Gly161Asp)not specified [RCV005354402]uncertain significance2176100283176100283Humanname
598192182CV3971808single nucleotide variantNM_021193.4(HOXD12):c.352T>C (p.Ser118Pro)not specified [RCV005354403]likely benign2176100153176100153Humanname
598192190CV3971809single nucleotide variantNM_021193.4(HOXD12):c.509T>C (p.Leu170Pro)not specified [RCV005354404]uncertain significance2176100310176100310Humanname
598192198CV3971810single nucleotide variantNM_021193.4(HOXD12):c.648G>C (p.Glu216Asp)not specified [RCV005354405]uncertain significance2176100595176100595Humanname