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72 records found for search term Xkr5
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407455891CV3488198single nucleotide variantNM_207411.5(XKR5):c.7G>A (p.Ala3Thr)not specified [RCV004685739]uncertain significance868354876835487Humanname
407455888CV3488197single nucleotide variantNM_207411.5(XKR5):c.26C>T (p.Ser9Leu)not specified [RCV004685738]uncertain significance868354686835468Humanname
598275752CV3933655single nucleotide variantNM_207411.5(XKR5):c.22C>A (p.Leu8Ile)not specified [RCV005304886]uncertain significance868354726835472Humanname
329394022CV2472274single nucleotide variantNM_207411.5(XKR5):c.56C>A (p.Ala19Glu)not specified [RCV004283379]uncertain significance868354386835438Humanname
401730829CV2711518single nucleotide variantNM_207411.5(XKR5):c.29C>T (p.Ala10Val)not specified [RCV004306833]uncertain significance868354656835465Humanname
401860909CV2772293single nucleotide variantNM_207411.5(XKR5):c.65A>T (p.Tyr22Phe)not specified [RCV004353314]uncertain significance868328946832894Humanname
405666255CV3349507single nucleotide variantNM_207411.5(XKR5):c.70G>A (p.Val24Met)not specified [RCV004485534]uncertain significance868328896832889Humanname
407455902CV3488202single nucleotide variantNM_207411.5(XKR5):c.51G>T (p.Gln17His)not specified [RCV004685743]uncertain significance868354436835443Humanname
597804559CV3634186single nucleotide variantNM_207411.5(XKR5):c.44C>A (p.Ala15Asp)not specified [RCV004882316]uncertain significance868354506835450Humanname
8633058CV88272single nucleotide variantNM_207411.4(XKR5):c.68C>T (p.Thr23Ile)Malignant melanoma [RCV000068364]not provided868328916832891Humanname
156367266CV2266762single nucleotide variantNM_207411.5(XKR5):c.184C>A (p.His62Asn)not specified [RCV004137588]uncertain significance868327756832775Humanname
156268216CV2296797single nucleotide variantNM_207411.5(XKR5):c.229G>C (p.Gly77Arg)not specified [RCV004148692]uncertain significance868327306832730Humanname
156279127CV2325204single nucleotide variantNM_207411.5(XKR5):c.136G>A (p.Gly46Arg)not specified [RCV004177616]uncertain significance868328236832823Humanname
155906729CV2379115single nucleotide variantNM_207411.5(XKR5):c.248G>T (p.Trp83Leu)not specified [RCV004235912]uncertain significance868253446825344Humanname
401740146CV2684278single nucleotide variantNM_207411.5(XKR5):c.286G>T (p.Ala96Ser)not specified [RCV004288935]uncertain significance868253066825306Humanname
401764554CV2705087single nucleotide variantNM_207411.5(XKR5):c.253G>A (p.Ala85Thr)not specified [RCV004309997]uncertain significance868253396825339Humanname
401737966CV2714272single nucleotide variantNM_207411.5(XKR5):c.166T>C (p.Trp56Arg)not specified [RCV004315958]uncertain significance868327936832793Humanname
401781608CV2722183single nucleotide variantNM_207411.5(XKR5):c.124G>A (p.Val42Ile)not specified [RCV004328751]uncertain significance868328356832835Humanname
401871814CV2779411single nucleotide variantNM_207411.5(XKR5):c.159C>G (p.Ser53Arg)not specified [RCV004351054]uncertain significance868328006832800Humanname
401909174CV2820838single nucleotide variantNM_207411.5(XKR5):c.1149C>T (p.Val383=)not provided [RCV003423892]likely benign868121106812110Humanname
405666193CV3349493single nucleotide variantNM_207411.5(XKR5):c.118C>A (p.Leu40Ile)not specified [RCV004485520]uncertain significance868328416832841Humanname
405666201CV3349495single nucleotide variantNM_207411.5(XKR5):c.145G>A (p.Val49Ile)not specified [RCV004485522]uncertain significance868328146832814Humanname
407455884CV3488196single nucleotide variantNM_207411.5(XKR5):c.257C>T (p.Ala86Val)not specified [RCV004685737]likely benign868253356825335Humanname
597804556CV3634183single nucleotide variantNM_207411.5(XKR5):c.160T>C (p.Tyr54His)not specified [RCV004882314]uncertain significance868327996832799Humanname
597804567CV3634190single nucleotide variantNM_207411.5(XKR5):c.188C>G (p.Pro63Arg)not specified [RCV004882320]uncertain significance868327716832771Humanname
597804569CV3634191single nucleotide variantNM_207411.5(XKR5):c.100C>A (p.Leu34Met)not specified [RCV004882321]uncertain significance868328596832859Humanname
598275749CV3933651single nucleotide variantNM_207411.5(XKR5):c.197G>C (p.Cys66Ser)not specified [RCV005304883]uncertain significance868327626832762Humanname
598275750CV3933652single nucleotide variantNM_207411.5(XKR5):c.173G>A (p.Arg58Gln)not specified [RCV005304884]uncertain significance868327866832786Humanname
598182987CV3933654single nucleotide variantNM_207411.5(XKR5):c.210G>A (p.Met70Ile)not specified [RCV005311329]uncertain significance868327496832749Humanname
598275753CV3933656single nucleotide variantNM_207411.5(XKR5):c.214C>T (p.His72Tyr)not specified [RCV005304887]uncertain significance868327456832745Humanname
155985015CV2247823single nucleotide variantNM_207411.5(XKR5):c.338G>A (p.Arg113Gln)not specified [RCV004121287]uncertain significance868252546825254Humanname
155906072CV2303238single nucleotide variantNM_207411.5(XKR5):c.949C>G (p.Leu317Val)not specified [RCV004156991]uncertain significance868123106812310Humanname
155923646CV2351788single nucleotide variantNM_207411.5(XKR5):c.436A>G (p.Thr146Ala)not specified [RCV004197943]likely benign868237226823722Humanname
156100395CV2392941single nucleotide variantNM_207411.5(XKR5):c.592G>T (p.Val198Phe)not specified [RCV004247285]uncertain significance868235666823566Humanname
329353938CV2436679single nucleotide variantNM_207411.5(XKR5):c.419T>C (p.Ile140Thr)not specified [RCV004258051]uncertain significance868251736825173Humanname
329374806CV2440052single nucleotide variantNM_207411.5(XKR5):c.799T>C (p.Phe267Leu)not specified [RCV004260522]uncertain significance868218776821877Humanname
401758696CV2700704single nucleotide variantNM_207411.5(XKR5):c.845C>T (p.Ala282Val)not specified [RCV004313417]uncertain significance868158816815881Humanname
401749892CV2719438single nucleotide variantNM_207411.5(XKR5):c.865G>T (p.Ala289Ser)not specified [RCV004326839]uncertain significance868158616815861Humanname
401780046CV2725842single nucleotide variantNM_207411.5(XKR5):c.776C>T (p.Pro259Leu)not specified [RCV004316306]uncertain significance868219006821900Humanname
401758264CV2729628single nucleotide variantNM_207411.5(XKR5):c.684T>A (p.Ser228Arg)not specified [RCV004331890]uncertain significance868219926821992Humanname
401893599CV2763760single nucleotide variantNM_207411.5(XKR5):c.673G>A (p.Ala225Thr)not specified [RCV004343244]uncertain significance868220036822003Humanname
405666215CV3349498single nucleotide variantNM_207411.5(XKR5):c.379C>A (p.Leu127Ile)not specified [RCV004485525]uncertain significance868252136825213Humanname
405666220CV3349499single nucleotide variantNM_207411.5(XKR5):c.430G>A (p.Val144Met)not specified [RCV004485526]uncertain significance868237286823728Humanname
405666226CV3349500single nucleotide variantNM_207411.5(XKR5):c.523C>A (p.Pro175Thr)not specified [RCV004485527]uncertain significance868236356823635Humanname
405666231CV3349501single nucleotide variantNM_207411.5(XKR5):c.533C>A (p.Ala178Asp)not specified [RCV004485528]uncertain significance868236256823625Humanname
405666234CV3349502single nucleotide variantNM_207411.5(XKR5):c.578G>C (p.Arg193Pro)not specified [RCV004485529]uncertain significance868235806823580Humanname
405666238CV3349503single nucleotide variantNM_207411.5(XKR5):c.662T>C (p.Phe221Ser)not specified [RCV004485530]uncertain significance868220146822014Humanname
405666241CV3349504single nucleotide variantNM_207411.5(XKR5):c.663C>G (p.Phe221Leu)not specified [RCV004485531]uncertain significance868220136822013Humanname
405666246CV3349505single nucleotide variantNM_207411.5(XKR5):c.682A>T (p.Ser228Cys)not specified [RCV004485532]uncertain significance868219946821994Humanname
405666251CV3349506single nucleotide variantNM_207411.5(XKR5):c.694G>T (p.Asp232Tyr)not specified [RCV004485533]uncertain significance868219826821982Humanname
405666258CV3349508single nucleotide variantNM_207411.5(XKR5):c.851A>G (p.Asp284Gly)not specified [RCV004485535]uncertain significance868158756815875Humanname
407455878CV3488194single nucleotide variantNM_207411.5(XKR5):c.536T>A (p.Leu179His)not specified [RCV004685735]uncertain significance868236226823622Humanname
407455881CV3488195single nucleotide variantNM_207411.5(XKR5):c.532G>A (p.Ala178Thr)not specified [RCV004685736]uncertain significance868236266823626Humanname
407455894CV3488199single nucleotide variantNM_207411.5(XKR5):c.469C>A (p.Leu157Met)not specified [RCV004685740]uncertain significance868236896823689Humanname
407455899CV3488201single nucleotide variantNM_207411.5(XKR5):c.898G>A (p.Val300Ile)not specified [RCV004685742]uncertain significance868158286815828Humanname
597751389CV3634184single nucleotide variantNM_207411.5(XKR5):c.862G>A (p.Gly288Arg)not specified [RCV004892769]uncertain significance868158646815864Humanname
597804564CV3634188single nucleotide variantNM_207411.5(XKR5):c.850G>A (p.Asp284Asn)not specified [RCV004882318]uncertain significance868158766815876Humanname
597804566CV3634189single nucleotide variantNM_207411.5(XKR5):c.404C>T (p.Ser135Leu)not specified [RCV004882319]uncertain significance868251886825188Humanname
598182968CV3933647single nucleotide variantNM_207411.5(XKR5):c.694G>C (p.Asp232His)not specified [RCV005311326]uncertain significance868219826821982Humanname
598182974CV3933648single nucleotide variantNM_207411.5(XKR5):c.329C>T (p.Ser110Leu)not specified [RCV005311327]uncertain significance868252636825263Humanname
598275748CV3933649single nucleotide variantNM_207411.5(XKR5):c.701C>G (p.Thr234Ser)not specified [RCV005304882]uncertain significance868219756821975Humanname
598182981CV3933650single nucleotide variantNM_207411.5(XKR5):c.484C>T (p.Arg162Cys)not specified [RCV005311328]uncertain significance868236746823674Humanname
598275751CV3933653single nucleotide variantNM_207411.5(XKR5):c.450G>T (p.Trp150Cys)not specified [RCV005304885]uncertain significance868237086823708Humanname
598275754CV3933657single nucleotide variantNM_207411.5(XKR5):c.364G>A (p.Gly122Arg)not specified [RCV005304888]uncertain significance868252286825228Humanname
156015687CV2298948single nucleotide variantNM_207411.5(XKR5):c.1064G>C (p.Gly355Ala)not specified [RCV004156477]uncertain significance868121956812195Humanname
401770981CV2726322single nucleotide variantNM_207411.5(XKR5):c.1679C>G (p.Pro560Arg)not specified [RCV004326764]uncertain significance868115806811580Humanname
405666183CV3349491single nucleotide variantNM_207411.5(XKR5):c.1048G>A (p.Ala350Thr)not specified [RCV004485518]uncertain significance868122116812211Humanname
405666196CV3349494single nucleotide variantNM_207411.5(XKR5):c.1378C>G (p.Arg460Gly)not specified [RCV004485521]uncertain significance868118816811881Humanname
405666206CV3349496single nucleotide variantNM_207411.5(XKR5):c.1853G>C (p.Gly618Ala)not specified [RCV004485523]uncertain significance868114066811406Humanname
405666211CV3349497single nucleotide variantNM_207411.5(XKR5):c.2050T>C (p.Phe684Leu)not specified [RCV004485524]uncertain significance868112096811209Humanname
407455904CV3488203single nucleotide variantNM_207411.5(XKR5):c.1310G>A (p.Gly437Glu)not specified [RCV004685744]uncertain significance868119496811949Humanname
597804557CV3634185single nucleotide variantNM_207411.5(XKR5):c.1956G>C (p.Arg652Ser)not specified [RCV004882315]uncertain significance868113036811303Humanname