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)

69 records found for search term Parp12
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401909020CV2823187single nucleotide variantNM_022750.4(PARP12):c.1498-5T>Cnot provided [RCV003423775]likely benign7140027411140027411Humanname
405772939CV3364419single nucleotide variantNM_022750.4(PARP12):c.37G>A (p.Val13Met)not specified [RCV004502604]uncertain significance7140062811140062811Humanname
597658126CV3571551single nucleotide variantNM_022750.4(PARP12):c.76C>G (p.Leu26Val)not specified [RCV004827747]uncertain significance7140062772140062772Humanname
598243869CV4002081single nucleotide variantNM_022750.4(PARP12):c.40C>G (p.Leu14Val)not specified [RCV005383663]uncertain significance7140062808140062808Humanname
155987708CV2234128single nucleotide variantNM_022750.4(PARP12):c.188A>C (p.Glu63Ala)not specified [RCV004106222]uncertain significance7140062660140062660Humanname
155924445CV2358152single nucleotide variantNM_022750.4(PARP12):c.152T>G (p.Val51Gly)not specified [RCV004211954]uncertain significance7140062696140062696Humanname
156097464CV2375625single nucleotide variantNM_022750.4(PARP12):c.158T>G (p.Val53Gly)not specified [RCV004226106]uncertain significance7140062690140062690Humanname
329401203CV2442152single nucleotide variantNM_022750.4(PARP12):c.176C>T (p.Ala59Val)not specified [RCV004264657]uncertain significance7140062672140062672Humanname
401761735CV2699397single nucleotide variantNM_022750.4(PARP12):c.278A>T (p.His93Leu)not specified [RCV004305976]uncertain significance7140062570140062570Humanname
401897914CV2769671single nucleotide variantNM_022750.4(PARP12):c.284G>A (p.Cys95Tyr)not specified [RCV004351598]uncertain significance7140062564140062564Humanname
401885117CV2786680single nucleotide variantNM_022750.4(PARP12):c.185C>T (p.Pro62Leu)not specified [RCV004363806]uncertain significance7140062663140062663Humanname
405772933CV3364418single nucleotide variantNM_022750.4(PARP12):c.256G>T (p.Val86Leu)not specified [RCV004502603]uncertain significance7140062592140062592Humanname
407479671CV3466599single nucleotide variantNM_022750.4(PARP12):c.248C>T (p.Pro83Leu)not specified [RCV004664193]uncertain significance7140062600140062600Humanname
597658133CV3571556single nucleotide variantNM_022750.4(PARP12):c.190C>T (p.Arg64Cys)not specified [RCV004827748]uncertain significance7140062658140062658Humanname
597719329CV3571558single nucleotide variantNM_022750.4(PARP12):c.145T>C (p.Phe49Leu)not specified [RCV004841736]uncertain significance7140062703140062703Humanname
597719337CV3571560single nucleotide variantNM_022750.4(PARP12):c.189G>T (p.Glu63Asp)not specified [RCV004841737]uncertain significance7140062659140062659Humanname
597719343CV3571563single nucleotide variantNM_022750.4(PARP12):c.155C>T (p.Ala52Val)not specified [RCV004841738]uncertain significance7140062693140062693Humanname
15134053CV710825single nucleotide variantNM_022750.4(PARP12):c.1053C>T (p.Tyr351=)not provided [RCV000965060]benign7140041773140041773Humanname
15136877CV735990single nucleotide variantNM_022750.4(PARP12):c.1257G>T (p.Gly419=)not provided [RCV000898704]benign7140037782140037782Humanname
156214046CV2257433single nucleotide variantNM_022750.4(PARP12):c.367A>G (p.Asn123Asp)not specified [RCV004125512]uncertain significance7140057994140057994Humanname
155946197CV2266010single nucleotide variantNM_022750.4(PARP12):c.587A>G (p.Lys196Arg)not specified [RCV004126836]uncertain significance7140057029140057029Humanname
156104130CV2291686single nucleotide variantNM_022750.4(PARP12):c.751G>A (p.Gly251Arg)not specified [RCV004155969]uncertain significance7140056865140056865Humanname
155924938CV2348249single nucleotide variantNM_022750.4(PARP12):c.394G>A (p.Val132Ile)not specified [RCV004191289]uncertain significance7140057967140057967Humanname
156402115CV2368016single nucleotide variantNM_022750.4(PARP12):c.841C>T (p.Arg281Trp)not specified [RCV004223102]likely benign7140054683140054683Humanname
156251106CV2368717single nucleotide variantNM_022750.4(PARP12):c.842G>A (p.Arg281Gln)not specified [RCV004214602]uncertain significance7140054682140054682Humanname
401779596CV2718641single nucleotide variantNM_022750.4(PARP12):c.860A>T (p.Gln287Leu)not specified [RCV004320219]uncertain significance7140054664140054664Humanname
401764789CV2728079single nucleotide variantNM_022750.4(PARP12):c.950T>G (p.Leu317Arg)not specified [RCV004324184]uncertain significance7140046920140046920Humanname
405772947CV3364420single nucleotide variantNM_022750.4(PARP12):c.682A>G (p.Arg228Gly)not specified [RCV004502605]uncertain significance7140056934140056934Humanname
405772953CV3364421single nucleotide variantNM_022750.4(PARP12):c.683G>T (p.Arg228Ile)not specified [RCV004502606]uncertain significance7140056933140056933Humanname
405772960CV3364422single nucleotide variantNM_022750.4(PARP12):c.755C>G (p.Thr252Ser)not specified [RCV004502607]uncertain significance7140056861140056861Humanname
597719305CV3571554single nucleotide variantNM_022750.4(PARP12):c.548A>G (p.Tyr183Cys)not specified [RCV004841733]uncertain significance7140057068140057068Humanname
597719314CV3571555single nucleotide variantNM_022750.4(PARP12):c.304G>A (p.Ala102Thr)not specified [RCV004841734]uncertain significance7140062544140062544Humanname
597719320CV3571557single nucleotide variantNM_022750.4(PARP12):c.491G>C (p.Gly164Ala)not specified [RCV004841735]uncertain significance7140057125140057125Humanname
597658140CV3571559single nucleotide variantNM_022750.4(PARP12):c.640G>T (p.Gly214Cys)not specified [RCV004827749]uncertain significance7140056976140056976Humanname
597719350CV3571564single nucleotide variantNM_022750.4(PARP12):c.995G>A (p.Cys332Tyr)not specified [RCV004841739]uncertain significance7140041831140041831Humanname
598185149CV4002075single nucleotide variantNM_022750.4(PARP12):c.971A>G (p.Asn324Ser)not specified [RCV005395563]uncertain significance7140046899140046899Humanname
598243838CV4002077single nucleotide variantNM_022750.4(PARP12):c.674C>T (p.Thr225Ile)not specified [RCV005383659]uncertain significance7140056942140056942Humanname
598243860CV4002080single nucleotide variantNM_022750.4(PARP12):c.745C>T (p.Pro249Ser)not specified [RCV005383662]uncertain significance7140056871140056871Humanname
598243876CV4002083single nucleotide variantNM_022750.4(PARP12):c.340A>G (p.Asn114Asp)not specified [RCV005383664]uncertain significance7140058021140058021Humanname
15134060CV710826single nucleotide variantNM_022750.4(PARP12):c.359C>T (p.Thr120Ile)not provided [RCV000965061]benign7140058002140058002Humanname
156236149CV2224101single nucleotide variantNM_022750.4(PARP12):c.1894G>C (p.Ala632Pro)not specified [RCV004095965]uncertain significance7140024772140024772Humanname
156276231CV2330738single nucleotide variantNM_022750.4(PARP12):c.1025A>T (p.His342Leu)not specified [RCV004185802]uncertain significance7140041801140041801Humanname
156250197CV2359053single nucleotide variantNM_022750.4(PARP12):c.1213A>G (p.Ser405Gly)not specified [RCV004212375]uncertain significance7140037826140037826Humanname
156047722CV2390958single nucleotide variantNM_022750.4(PARP12):c.1100A>G (p.Lys367Arg)not specified [RCV004234965]uncertain significance7140041726140041726Humanname
156187159CV2397831single nucleotide variantNM_022750.4(PARP12):c.1678C>T (p.Arg560Trp)not specified [RCV004239302]uncertain significance7140026299140026299Humanname
156003296CV2399646single nucleotide variantNM_022750.4(PARP12):c.1657G>A (p.Gly553Arg)not specified [RCV004244161]uncertain significance7140026320140026320Humanname
329376932CV2435747single nucleotide variantNM_022750.4(PARP12):c.1434T>G (p.Phe478Leu)not specified [RCV004253376]uncertain significance7140028676140028676Humanname
401739041CV2673210single nucleotide variantNM_022750.4(PARP12):c.1555C>T (p.Arg519Cys)not specified [RCV004286018]uncertain significance7140027349140027349Humanname
401857240CV2760030single nucleotide variantNM_022750.4(PARP12):c.1168G>A (p.Glu390Lys)not specified [RCV004345442]uncertain significance7140041658140041658Humanname
401885292CV2768054single nucleotide variantNM_022750.4(PARP12):c.1796G>A (p.Arg599Gln)not specified [RCV004348293]uncertain significance7140024870140024870Humanname
405772880CV3364410single nucleotide variantNM_022750.4(PARP12):c.1066G>A (p.Ala356Thr)not specified [RCV004502595]uncertain significance7140041760140041760Humanname
405772887CV3364411single nucleotide variantNM_022750.4(PARP12):c.1505C>T (p.Thr502Ile)not specified [RCV004502596]uncertain significance7140027399140027399Humanname
405772893CV3364412single nucleotide variantNM_022750.4(PARP12):c.1663A>C (p.Lys555Gln)not specified [RCV004502597]uncertain significance7140026314140026314Humanname
405772899CV3364413single nucleotide variantNM_022750.4(PARP12):c.1702G>A (p.Ala568Thr)not specified [RCV004502598]likely benign7140026275140026275Humanname
405772913CV3364415single nucleotide variantNM_022750.4(PARP12):c.1831G>A (p.Asp611Asn)not specified [RCV004502600]uncertain significance7140024835140024835Humanname
405772919CV3364416single nucleotide variantNM_022750.4(PARP12):c.1882G>A (p.Val628Ile)not specified [RCV004502601]uncertain significance7140024784140024784Humanname
405772925CV3364417single nucleotide variantNM_022750.4(PARP12):c.2029T>C (p.Tyr677His)not specified [RCV004502602]uncertain significance7140024637140024637Humanname
407479667CV3466598single nucleotide variantNM_022750.4(PARP12):c.1189G>T (p.Val397Leu)not specified [RCV004664192]uncertain significance7140037850140037850Humanname
597719278CV3571550single nucleotide variantNM_022750.4(PARP12):c.1907G>A (p.Arg636His)not specified [RCV004841730]uncertain significance7140024759140024759Humanname
597719288CV3571552single nucleotide variantNM_022750.4(PARP12):c.1378C>T (p.Pro460Ser)not specified [RCV004841731]uncertain significance7140034278140034278Humanname
597719297CV3571553single nucleotide variantNM_022750.4(PARP12):c.1669G>A (p.Val557Met)not specified [RCV004841732]uncertain significance7140026308140026308Humanname
597658145CV3571561single nucleotide variantNM_022750.4(PARP12):c.1661G>A (p.Gly554Glu)not specified [RCV004827750]uncertain significance7140026316140026316Humanname
597658152CV3571562single nucleotide variantNM_022750.4(PARP12):c.1472C>G (p.Ser491Cys)not specified [RCV004827751]uncertain significance7140028638140028638Humanname
597719358CV3571565single nucleotide variantNM_022750.4(PARP12):c.1307A>G (p.Tyr436Cys)not specified [RCV004841740]uncertain significance7140037732140037732Humanname
598243824CV4002073single nucleotide variantNM_022750.4(PARP12):c.1720A>G (p.Ile574Val)not specified [RCV005383657]uncertain significance7140026257140026257Humanname
598243831CV4002076single nucleotide variantNM_022750.4(PARP12):c.1157G>A (p.Gly386Asp)not specified [RCV005383658]uncertain significance7140041669140041669Humanname
598243846CV4002078single nucleotide variantNM_022750.4(PARP12):c.1435C>G (p.Pro479Ala)not specified [RCV005383660]uncertain significance7140028675140028675Humanname
598243852CV4002079single nucleotide variantNM_022750.4(PARP12):c.1999C>T (p.His667Tyr)not specified [RCV005383661]uncertain significance7140024667140024667Humanname
598185155CV4002082single nucleotide variantNM_022750.4(PARP12):c.1667C>T (p.Ala556Val)not specified [RCV005395564]uncertain significance7140026310140026310Humanname