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30 records found for search term Gpr63
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8582314CV116783single nucleotide variantNM_001143957.2(GPR63):c.*66T>ALung cancer [RCV000097306]uncertain significance69679840696798406Humanname
407526694CV3436780single nucleotide variantNM_030784.4(GPR63):c.17T>A (p.Val6Glu)not specified [RCV004632528]uncertain significance69679971596799715Humanname
597769759CV3681595single nucleotide variantNM_030784.4(GPR63):c.91C>T (p.Leu31Phe)not specified [RCV004928138]uncertain significance69679964196799641Humanname
597745428CV3681597single nucleotide variantNM_030784.4(GPR63):c.52A>G (p.Thr18Ala)not specified [RCV004922472]uncertain significance69679968096799680Humanname
598274646CV3967366single nucleotide variantNM_030784.4(GPR63):c.37G>C (p.Gly13Arg)not specified [RCV005351518]uncertain significance69679969596799695Humanname
155905593CV2303145single nucleotide variantNM_030784.4(GPR63):c.184A>T (p.Asn62Tyr)not specified [RCV004156914]uncertain significance69679954896799548Humanname
405739722CV3252067single nucleotide variantNM_030784.4(GPR63):c.209C>G (p.Pro70Arg)not specified [RCV004391151]uncertain significance69679952396799523Humanname
407526698CV3436781single nucleotide variantNM_030784.4(GPR63):c.277T>A (p.Phe93Ile)not specified [RCV004632529]uncertain significance69679945596799455Humanname
156367435CV2203519single nucleotide variantNM_030784.4(GPR63):c.904A>G (p.Met302Val)not specified [RCV004072724]uncertain significance69679882896798828Humanname
156029753CV2206101single nucleotide variantNM_030784.4(GPR63):c.355C>T (p.Leu119Phe)not specified [RCV004078510]uncertain significance69679937796799377Humanname
155999627CV2396447single nucleotide variantNM_030784.4(GPR63):c.346A>G (p.Ile116Val)not specified [RCV004242160]uncertain significance69679938696799386Humanname
329393659CV2472061single nucleotide variantNM_030784.4(GPR63):c.973G>T (p.Val325Phe)not specified [RCV004283202]uncertain significance69679875996798759Humanname
401774329CV2727806single nucleotide variantNM_030784.4(GPR63):c.788T>C (p.Met263Thr)not specified [RCV004323831]uncertain significance69679894496798944Humanname
405739730CV3252068single nucleotide variantNM_030784.4(GPR63):c.466G>T (p.Val156Leu)not specified [RCV004391152]uncertain significance69679926696799266Humanname
405739736CV3252069single nucleotide variantNM_030784.4(GPR63):c.700A>C (p.Thr234Pro)not specified [RCV004391153]uncertain significance69679903296799032Humanname
405739754CV3252071single nucleotide variantNM_030784.4(GPR63):c.757A>G (p.Ile253Val)not specified [RCV004391155]uncertain significance69679897596798975Humanname
407526701CV3436782single nucleotide variantNM_030784.4(GPR63):c.605C>T (p.Ser202Phe)not specified [RCV004632530]uncertain significance69679912796799127Humanname
407526708CV3436784single nucleotide variantNM_030784.4(GPR63):c.877C>T (p.Leu293Phe)not specified [RCV004632532]uncertain significance69679885596798855Humanname
407526711CV3436785single nucleotide variantNM_030784.4(GPR63):c.527G>A (p.Ser176Asn)not specified [RCV004632533]uncertain significance69679920596799205Humanname
597769764CV3681596single nucleotide variantNM_030784.4(GPR63):c.838C>T (p.Pro280Ser)not specified [RCV004928139]uncertain significance69679889496798894Humanname
597769768CV3681598single nucleotide variantNM_030784.4(GPR63):c.995C>G (p.Thr332Ser)not specified [RCV004928140]uncertain significance69679873796798737Humanname
597769771CV3681599single nucleotide variantNM_030784.4(GPR63):c.479T>G (p.Phe160Cys)not specified [RCV004928141]uncertain significance69679925396799253Humanname
598274640CV3967363single nucleotide variantNM_030784.4(GPR63):c.830A>G (p.His277Arg)not specified [RCV005351515]uncertain significance69679890296798902Humanname
598274644CV3967365single nucleotide variantNM_030784.4(GPR63):c.692T>C (p.Phe231Ser)not specified [RCV005351517]uncertain significance69679904096799040Humanname
155916123CV2239659single nucleotide variantNM_030784.4(GPR63):c.1229A>G (p.Tyr410Cys)not specified [RCV004108209]uncertain significance69679850396798503Humanname
156081248CV2256062single nucleotide variantNM_030784.4(GPR63):c.1208G>A (p.Arg403Gln)not specified [RCV004116358]uncertain significance69679852496798524Humanname
329397448CV2466202single nucleotide variantNM_030784.4(GPR63):c.1246C>T (p.Arg416Trp)not specified [RCV004279844]uncertain significance69679848696798486Humanname
405739715CV3252066single nucleotide variantNM_030784.4(GPR63):c.1181C>T (p.Pro394Leu)not specified [RCV004391150]uncertain significance69679855196798551Humanname
598274638CV3967362single nucleotide variantNM_030784.4(GPR63):c.1180C>T (p.Pro394Ser)not specified [RCV005351514]uncertain significance69679855296798552Humanname
598274642CV3967364single nucleotide variantNM_030784.4(GPR63):c.1235G>A (p.Cys412Tyr)not specified [RCV005351516]uncertain significance69679849796798497Humanname