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73 records found for search term Serinc2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15166743CV707338single nucleotide variantNM_178865.5(SERINC2):c.228C>T (p.Ala76=)not provided [RCV000971249]benign13142470931424709Humanname
597737795CV3598447single nucleotide variantNM_178865.5(SERINC2):c.91G>A (p.Ala31Thr)not specified [RCV004864112]uncertain significance13142374431423744Humanname
156209255CV2250195single nucleotide variantNM_178865.5(SERINC2):c.209G>C (p.Trp70Ser)not specified [RCV004116992]uncertain significance13142469031424690Humanname
155949008CV2273597single nucleotide variantNM_178865.5(SERINC2):c.281A>G (p.Tyr94Cys)not specified [RCV004134116]uncertain significance13142476231424762Humanname
156092615CV2381907single nucleotide variantNM_178865.5(SERINC2):c.206C>T (p.Pro69Leu)not specified [RCV004225847]uncertain significance13142468731424687Humanname
329376452CV2425142single nucleotide variantNM_178865.5(SERINC2):c.181G>A (p.Val61Met)not specified [RCV004249032]uncertain significance13142383431423834Humanname
401740246CV2684307single nucleotide variantNM_178865.5(SERINC2):c.224G>A (p.Gly75Glu)not specified [RCV004288960]uncertain significance13142470531424705Humanname
401878648CV2767482single nucleotide variantNM_178865.5(SERINC2):c.241G>A (p.Val81Ile)not specified [RCV004343646]likely benign13142472231424722Humanname
401927388CV2812586single nucleotide variantNM_178865.5(SERINC2):c.1263G>A (p.Thr421=)not provided [RCV003406278]likely benign13143409431434094Humanname
405867039CV2842581single nucleotide variantNM_178865.5(SERINC2):c.115C>T (p.Arg39Cys)EBV-positive nodal T- and NK-cell lymphoma [RCV004557938]likely benign13142376831423768Humanname
405746650CV3310856single nucleotide variantNM_178865.5(SERINC2):c.284G>A (p.Arg95His)not specified [RCV004453156]uncertain significance13142476531424765Humanname
405746658CV3310857single nucleotide variantNM_178865.5(SERINC2):c.295C>T (p.Arg99Cys)not specified [RCV004453157]uncertain significance13142477631424776Humanname
405746667CV3310858single nucleotide variantNM_178865.5(SERINC2):c.296G>A (p.Arg99His)not specified [RCV004453158]uncertain significance13142477731424777Humanname
597737766CV3598441single nucleotide variantNM_178865.5(SERINC2):c.149T>A (p.Val50Glu)not specified [RCV004864106]uncertain significance13142380231423802Humanname
597737777CV3598443single nucleotide variantNM_178865.5(SERINC2):c.265G>C (p.Gly89Arg)not specified [RCV004864108]uncertain significance13142474631424746Humanname
597737799CV3598448single nucleotide variantNM_178865.5(SERINC2):c.194T>C (p.Leu65Pro)not specified [RCV004864113]uncertain significance13142384731423847Humanname
597737812CV3598451single nucleotide variantNM_178865.5(SERINC2):c.192G>C (p.Gln64His)not specified [RCV004864116]uncertain significance13142384531423845Humanname
598225426CV3900383single nucleotide variantNM_178865.5(SERINC2):c.160A>T (p.Ile54Phe)not specified [RCV005273350]uncertain significance13142381331423813Humanname
15150276CV707339single nucleotide variantNM_178865.5(SERINC2):c.259G>A (p.Asp87Asn)not provided [RCV000967912]benign13142474031424740Humanname
155920627CV2210853single nucleotide variantNM_178865.5(SERINC2):c.580G>A (p.Glu194Lys)not specified [RCV004085940]uncertain significance13142588331425883Humanname
156037205CV2243747single nucleotide variantNM_178865.5(SERINC2):c.658G>A (p.Val220Met)not specified [RCV004114445]uncertain significance13142670131426701Humanname
156313399CV2257008single nucleotide variantNM_178865.5(SERINC2):c.613C>T (p.Leu205Phe)not specified [RCV004121192]uncertain significance13142665631426656Humanname
156362418CV2265525single nucleotide variantNM_178865.5(SERINC2):c.607G>A (p.Ala203Thr)not specified [RCV004124277]uncertain significance13142591031425910Humanname
155947921CV2271908single nucleotide variantNM_178865.5(SERINC2):c.326T>C (p.Phe109Ser)not specified [RCV004124735]uncertain significance13142480731424807Humanname
156269761CV2315049single nucleotide variantNM_178865.5(SERINC2):c.830A>C (p.Tyr277Ser)not specified [RCV004164958]uncertain significance13142902731429027Humanname
156221263CV2343822single nucleotide variantNM_178865.5(SERINC2):c.382A>T (p.Ile128Phe)not specified [RCV004193408]uncertain significance13142486331424863Humanname
155927137CV2365879single nucleotide variantNM_178865.5(SERINC2):c.595C>T (p.Arg199Cys)not specified [RCV004214408]uncertain significance13142589831425898Humanname
156384608CV2371509single nucleotide variantNM_178865.5(SERINC2):c.563G>C (p.Arg188Pro)not specified [RCV004216763]uncertain significance13142586631425866Humanname
156154421CV2388710single nucleotide variantNM_178865.5(SERINC2):c.749T>C (p.Val250Ala)not specified [RCV004239580]uncertain significance13142679231426792Humanname
156155438CV2388785single nucleotide variantNM_178865.5(SERINC2):c.344T>C (p.Met115Thr)not specified [RCV004239641]uncertain significance13142482531424825Humanname
156155450CV2388786single nucleotide variantNM_178865.5(SERINC2):c.347T>A (p.Leu116His)not specified [RCV004239642]uncertain significance13142482831424828Humanname
156155467CV2388787single nucleotide variantNM_178865.5(SERINC2):c.349T>A (p.Cys117Ser)not specified [RCV004239643]uncertain significance13142483031424830Humanname
156155485CV2388788single nucleotide variantNM_178865.5(SERINC2):c.352G>A (p.Val118Met)not specified [RCV004239644]uncertain significance13142483331424833Humanname
156262620CV2391603single nucleotide variantNM_178865.5(SERINC2):c.433G>A (p.Val145Met)not specified [RCV004239979]uncertain significance13142537031425370Humanname
329356101CV2445614single nucleotide variantNM_178865.5(SERINC2):c.596G>A (p.Arg199His)not specified [RCV004259698]uncertain significance13142589931425899Humanname
401743217CV2677796single nucleotide variantNM_178865.5(SERINC2):c.373C>T (p.Arg125Trp)not specified [RCV004293911]uncertain significance13142485431424854Humanname
401862044CV2766569single nucleotide variantNM_178865.5(SERINC2):c.457G>A (p.Gly153Ser)not specified [RCV004347187]uncertain significance13142539431425394Humanname
401927386CV2812584single nucleotide variantNM_178865.5(SERINC2):c.364C>G (p.Arg122Gly)not provided [RCV003406276]likely benign13142484531424845Humanname
401927387CV2812585single nucleotide variantNM_178865.5(SERINC2):c.364C>T (p.Arg122Trp)not provided [RCV003406277]likely benign13142484531424845Humanname
405746676CV3310859single nucleotide variantNM_178865.5(SERINC2):c.437G>A (p.Gly146Asp)not specified [RCV004453159]uncertain significance13142537431425374Humanname
405746685CV3310860single nucleotide variantNM_178865.5(SERINC2):c.547C>T (p.His183Tyr)not specified [RCV004453160]uncertain significance13142585031425850Humanname
405746698CV3310861single nucleotide variantNM_178865.5(SERINC2):c.703G>A (p.Glu235Lys)not specified [RCV004453161]uncertain significance13142674631426746Humanname
405746707CV3310862single nucleotide variantNM_178865.5(SERINC2):c.886C>A (p.Pro296Thr)not specified [RCV004453162]uncertain significance13142941131429411Humanname
405746716CV3310863single nucleotide variantNM_178865.5(SERINC2):c.913G>A (p.Glu305Lys)not specified [RCV004453163]uncertain significance13142943831429438Humanname
597737781CV3598444single nucleotide variantNM_178865.5(SERINC2):c.365G>A (p.Arg122Gln)not specified [RCV004864109]uncertain significance13142484631424846Humanname
597737791CV3598446single nucleotide variantNM_178865.5(SERINC2):c.797C>T (p.Ser266Leu)not specified [RCV004864111]uncertain significance13142899431428994Humanname
598225395CV3900378single nucleotide variantNM_178865.5(SERINC2):c.908G>T (p.Gly303Val)not specified [RCV005273345]uncertain significance13142943331429433Humanname
598225419CV3900382single nucleotide variantNM_178865.5(SERINC2):c.403T>C (p.Phe135Leu)not specified [RCV005273349]uncertain significance13142534031425340Humanname
156366864CV2203420single nucleotide variantNM_178865.5(SERINC2):c.1033C>T (p.Arg345Trp)not specified [RCV004072640]uncertain significance13143298631432986Humanname
156189215CV2258485single nucleotide variantNM_178865.5(SERINC2):c.1084G>A (p.Ala362Thr)not specified [RCV004115670]uncertain significance13143303731433037Humanname
155915744CV2274363single nucleotide variantNM_178865.5(SERINC2):c.1018C>T (p.Arg340Cys)not specified [RCV004136746]uncertain significance13143297131432971Humanname
156194085CV2350689single nucleotide variantNM_178865.5(SERINC2):c.1019G>A (p.Arg340His)not specified [RCV004207038]uncertain significance13143297231432972Humanname
156173093CV2355141single nucleotide variantNM_178865.5(SERINC2):c.1334C>T (p.Ala445Val)not specified [RCV004198531]uncertain significance13143416531434165Humanname
156109722CV2355517single nucleotide variantNM_178865.5(SERINC2):c.1142A>G (p.Gln381Arg)not specified [RCV004205367]uncertain significance13143309531433095Humanname
401771208CV2675497single nucleotide variantNM_178865.5(SERINC2):c.1150G>A (p.Val384Ile)not specified [RCV004295115]uncertain significance13143310331433103Humanname
401724910CV2686629single nucleotide variantNM_178865.5(SERINC2):c.1204G>A (p.Val402Ile)not specified [RCV004300046]likely benign13143315731433157Humanname
401875228CV2756293single nucleotide variantNM_178865.5(SERINC2):c.1147G>A (p.Gly383Ser)not specified [RCV004338382]uncertain significance13143310031433100Humanname
401881036CV2763219single nucleotide variantNM_178865.5(SERINC2):c.1034G>A (p.Arg345Gln)not specified [RCV004336254]uncertain significance13143298731432987Humanname
405746598CV3310850single nucleotide variantNM_178865.5(SERINC2):c.1124G>A (p.Arg375Gln)not specified [RCV004453150]uncertain significance13143307731433077Humanname
405746605CV3310851single nucleotide variantNM_178865.5(SERINC2):c.1212G>A (p.Met404Ile)not specified [RCV004453151]uncertain significance13143316531433165Humanname
405746613CV3310852single nucleotide variantNM_178865.5(SERINC2):c.1237G>A (p.Gly413Ser)not specified [RCV004453152]uncertain significance13143406831434068Humanname
405746621CV3310853single nucleotide variantNM_178865.5(SERINC2):c.1270G>A (p.Ala424Thr)not specified [RCV004453153]uncertain significance13143410131434101Humanname
405746639CV3310855single nucleotide variantNM_178865.5(SERINC2):c.1354C>T (p.Arg452Cys)not specified [RCV004453155]uncertain significance13143418531434185Humanname
407488775CV3473609single nucleotide variantNM_178865.5(SERINC2):c.1214C>T (p.Thr405Met)not specified [RCV004665929]uncertain significance13143316731433167Humanname
597737772CV3598442single nucleotide variantNM_178865.5(SERINC2):c.1348C>T (p.Arg450Cys)not specified [RCV004864107]uncertain significance13143417931434179Humanname
597737786CV3598445single nucleotide variantNM_178865.5(SERINC2):c.1137C>G (p.Asn379Lys)not specified [RCV004864110]uncertain significance13143309031433090Humanname
597737804CV3598449single nucleotide variantNM_178865.5(SERINC2):c.1339C>T (p.Leu447Phe)not specified [RCV004864114]uncertain significance13143417031434170Humanname
597737808CV3598450single nucleotide variantNM_178865.5(SERINC2):c.1073C>G (p.Pro358Arg)not specified [RCV004864115]uncertain significance13143302631433026Humanname
597737817CV3598452single nucleotide variantNM_178865.5(SERINC2):c.1000A>G (p.Thr334Ala)not specified [RCV004864117]uncertain significance13142952531429525Humanname
598225401CV3900379single nucleotide variantNM_178865.5(SERINC2):c.1328T>A (p.Leu443Gln)not specified [RCV005273346]uncertain significance13143415931434159Humanname
598225407CV3900380single nucleotide variantNM_178865.5(SERINC2):c.1319T>C (p.Leu440Pro)not specified [RCV005273347]uncertain significance13143415031434150Humanname
598225413CV3900381single nucleotide variantNM_178865.5(SERINC2):c.1355G>A (p.Arg452His)not specified [RCV005273348]uncertain significance13143418631434186Humanname
15159767CV707340deletionNM_178865.5(SERINC2):c.888_889del (p.His297fs)not provided [RCV000969770]benign13142941031429411Humanname