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49 records found for search term Ubqlnl
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405800264CV3337677single nucleotide variantNM_145053.5(UBQLNL):c.20G>A (p.Arg7Gln)not specified [RCV004477064]uncertain significance1155164225516422Humanname
405800263CV3337678single nucleotide variantNM_145053.5(UBQLNL):c.23C>T (p.Thr8Ile)not specified [RCV004477065]uncertain significance1155164195516419Humanname
407522954CV3491145single nucleotide variantNM_145053.5(UBQLNL):c.83C>T (p.Ser28Leu)not specified [RCV004677876]uncertain significance1155163595516359Humanname
597684499CV3626032single nucleotide variantNM_145053.5(UBQLNL):c.79T>C (p.Ser27Pro)not specified [RCV004883844]uncertain significance1155163635516363Humanname
156079608CV2226558single nucleotide variantNM_145053.5(UBQLNL):c.150C>G (p.Ile50Met)not specified [RCV004101815]uncertain significance1155162925516292Humanname
156032037CV2259483single nucleotide variantNM_145053.5(UBQLNL):c.206A>G (p.Gln69Arg)not specified [RCV004122685]uncertain significance1155162365516236Humanname
156281774CV2288770single nucleotide variantNM_145053.5(UBQLNL):c.197A>G (p.Gln66Arg)not specified [RCV004147987]uncertain significance1155162455516245Humanname
156186066CV2332484single nucleotide variantNM_145053.5(UBQLNL):c.243C>A (p.Asp81Glu)not specified [RCV004196209]uncertain significance1155161995516199Humanname
156304852CV2338570single nucleotide variantNM_145053.5(UBQLNL):c.152C>T (p.Ser51Leu)not specified [RCV004182164]uncertain significance1155162905516290Humanname
156111236CV2353319single nucleotide variantNM_145053.5(UBQLNL):c.154G>A (p.Val52Ile)not specified [RCV004205788]uncertain significance1155162885516288Humanname
407522943CV3491142single nucleotide variantNM_145053.5(UBQLNL):c.174G>A (p.Met58Ile)not specified [RCV004677873]uncertain significance1155162685516268Humanname
407522946CV3491143single nucleotide variantNM_145053.5(UBQLNL):c.284C>T (p.Thr95Ile)not specified [RCV004677874]uncertain significance1155161585516158Humanname
597684471CV3626035single nucleotide variantNM_145053.5(UBQLNL):c.101T>C (p.Ile34Thr)not specified [RCV004883847]uncertain significance1155163415516341Humanname
156400754CV2217128single nucleotide variantNM_145053.5(UBQLNL):c.821A>G (p.Tyr274Cys)not specified [RCV004085800]likely benign1155156215515621Humanname
156081316CV2333749single nucleotide variantNM_145053.5(UBQLNL):c.572T>C (p.Met191Thr)not specified [RCV004181260]uncertain significance1155158705515870Humanname
155932124CV2360093single nucleotide variantNM_145053.5(UBQLNL):c.882C>A (p.Phe294Leu)not specified [RCV004215370]uncertain significance1155155605515560Humanname
156004971CV2397016single nucleotide variantNM_145053.5(UBQLNL):c.766C>T (p.Pro256Ser)not specified [RCV004236168]likely benign1155156765515676Humanname
156003494CV2400889single nucleotide variantNM_145053.5(UBQLNL):c.876C>A (p.Asn292Lys)not specified [RCV004244181]uncertain significance1155155665515566Humanname
329349674CV2439268single nucleotide variantNM_145053.5(UBQLNL):c.340C>T (p.Arg114Trp)not specified [RCV004255549]uncertain significance1155161025516102Humanname
329350247CV2455953single nucleotide variantNM_145053.5(UBQLNL):c.574T>C (p.Trp192Arg)not specified [RCV004279214]likely benign1155158685515868Humanname
401748880CV2715080single nucleotide variantNM_145053.5(UBQLNL):c.587C>T (p.Ser196Leu)not specified [RCV004322665]uncertain significance1155158555515855Humanname
401749581CV2721038single nucleotide variantNM_145053.5(UBQLNL):c.371G>A (p.Arg124Gln)not specified [RCV004328314]likely benign1155160715516071Humanname
405800261CV3337679single nucleotide variantNM_145053.5(UBQLNL):c.547C>T (p.Arg183Trp)not specified [RCV004477066]uncertain significance1155158955515895Humanname
405800259CV3337680single nucleotide variantNM_145053.5(UBQLNL):c.554T>C (p.Leu185Pro)not specified [RCV004477067]uncertain significance1155158885515888Humanname
405800257CV3337681single nucleotide variantNM_145053.5(UBQLNL):c.649G>T (p.Asp217Tyr)not specified [RCV004477068]uncertain significance1155157935515793Humanname
405800255CV3337682single nucleotide variantNM_145053.5(UBQLNL):c.764A>C (p.Gln255Pro)not specified [RCV004477069]uncertain significance1155156785515678Humanname
405800253CV3337683single nucleotide variantNM_145053.5(UBQLNL):c.931C>A (p.Pro311Thr)not specified [RCV004477070]uncertain significance1155155115515511Humanname
405800251CV3337684single nucleotide variantNM_145053.5(UBQLNL):c.961G>T (p.Asp321Tyr)not specified [RCV004477071]uncertain significance1155154815515481Humanname
407522940CV3491141single nucleotide variantNM_145053.5(UBQLNL):c.715A>C (p.Met239Leu)not specified [RCV004677872]uncertain significance1155157275515727Humanname
407522950CV3491144single nucleotide variantNM_145053.5(UBQLNL):c.700A>G (p.Met234Val)not specified [RCV004677875]uncertain significance1155157425515742Humanname
597684460CV3622579single nucleotide variantNM_145053.5(UBQLNL):c.698C>G (p.Ala233Gly)not specified [RCV004883848]uncertain significance1155157445515744Humanname
597684519CV3626030single nucleotide variantNM_145053.5(UBQLNL):c.341G>A (p.Arg114Gln)not specified [RCV004883842]likely benign1155161015516101Humanname
15189968CV724483single nucleotide variantNM_145053.5(UBQLNL):c.913C>T (p.Gln305Ter)not provided [RCV000887971]benign1155155295515529Humanname
156302253CV2258634single nucleotide variantNM_145053.5(UBQLNL):c.1169A>C (p.Gln390Pro)not specified [RCV004117891]uncertain significance1155152735515273Humanname
156285107CV2360746single nucleotide variantNM_145053.5(UBQLNL):c.1364A>T (p.Gln455Leu)not specified [RCV004213530]uncertain significance1155150785515078Humanname
401746960CV2675367single nucleotide variantNM_145053.5(UBQLNL):c.1145C>G (p.Ala382Gly)not specified [RCV004292175]uncertain significance1155152975515297Humanname
401745667CV2676841single nucleotide variantNM_145053.5(UBQLNL):c.1151C>T (p.Pro384Leu)not specified [RCV004291008]uncertain significance1155152915515291Humanname
401745581CV2721510single nucleotide variantNM_145053.5(UBQLNL):c.1009G>C (p.Gly337Arg)not specified [RCV004316026]uncertain significance1155154335515433Humanname
405800268CV3337675single nucleotide variantNM_145053.5(UBQLNL):c.1343G>T (p.Ser448Ile)not specified [RCV004477062]uncertain significance1155150995515099Humanname
405800266CV3337676single nucleotide variantNM_145053.5(UBQLNL):c.1347G>A (p.Met449Ile)not specified [RCV004477063]uncertain significance1155150955515095Humanname
407462346CV3491140single nucleotide variantNM_145053.5(UBQLNL):c.1138A>T (p.Ile380Leu)not specified [RCV004687928]uncertain significance1155153045515304Humanname
597684537CV3626028single nucleotide variantNM_145053.5(UBQLNL):c.1079C>T (p.Thr360Ile)not specified [RCV004883840]uncertain significance1155153635515363Humanname
597684509CV3626031single nucleotide variantNM_145053.5(UBQLNL):c.1334T>G (p.Leu445Trp)not specified [RCV004883843]uncertain significance1155151085515108Humanname
597684491CV3626033single nucleotide variantNM_145053.5(UBQLNL):c.1309C>T (p.Pro437Ser)not specified [RCV004883845]uncertain significance1155151335515133Humanname
597684481CV3626034single nucleotide variantNM_145053.5(UBQLNL):c.1156A>C (p.Ile386Leu)not specified [RCV004883846]uncertain significance1155152865515286Humanname
598189547CV3928964single nucleotide variantNM_145053.5(UBQLNL):c.1159G>C (p.Glu387Gln)not specified [RCV005288087]uncertain significance1155152835515283Humanname
15189964CV724482single nucleotide variantNM_145053.5(UBQLNL):c.1124G>A (p.Arg375Gln)not provided [RCV000887970]benign1155153185515318Humanname
8627037CV82181single nucleotide variantNM_145053.4(UBQLNL):c.1082C>T (p.Ala361Val)Malignant melanoma [RCV000062260]not provided1155153605515360Humanname
15160063CV724484deletionNM_145053.5(UBQLNL):c.223_235del (p.Met75fs)not provided [RCV000881311]benign1155162075516219Humanname