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Variants search result for Homo sapiens
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69 records found for search term Parp12
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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