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Variants search result for Homo sapiens
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60 records found for search term Xrn2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8586341CV120940single nucleotide variantNM_012255.3(XRN2):c.2256-1146A>CLung cancer [RCV000101460]uncertain significance202136427521364275Humanname
155971945CV2214210single nucleotide variantNM_012255.5(XRN2):c.880C>T (p.Leu294Phe)not specified [RCV004086205]uncertain significance202133356521333565Humanname
155990956CV2281019single nucleotide variantNM_012255.5(XRN2):c.709A>G (p.Ile237Val)not specified [RCV004145509]uncertain significance202133229121332291Humanname
156000077CV2296270single nucleotide variantNM_012255.5(XRN2):c.523C>T (p.Arg175Cys)not specified [RCV004154173]uncertain significance202133065221330652Humanname
156266949CV2304948single nucleotide variantNM_012255.5(XRN2):c.797G>A (p.Cys266Tyr)not specified [RCV004168851]uncertain significance202133237921332379Humanname
156259982CV2322269single nucleotide variantNM_012255.5(XRN2):c.674C>T (p.Thr225Ile)not specified [RCV004176037]uncertain significance202133179221331792Humanname
156173365CV2377095single nucleotide variantNM_012255.5(XRN2):c.842G>A (p.Arg281Lys)not specified [RCV004229767]uncertain significance202133242421332424Humanname
329389883CV2457240single nucleotide variantNM_012255.5(XRN2):c.457G>C (p.Glu153Gln)not specified [RCV004265309]uncertain significance202133051021330510Humanname
401730295CV2711182single nucleotide variantNM_012255.5(XRN2):c.542G>A (p.Arg181His)not specified [RCV004312981]uncertain significance202133067121330671Humanname
401744037CV2722370single nucleotide variantNM_012255.5(XRN2):c.737C>T (p.Pro246Leu)not specified [RCV004322778]uncertain significance202133231921332319Humanname
405667183CV3349696single nucleotide variantNM_012255.5(XRN2):c.806T>A (p.Phe269Tyr)not specified [RCV004485723]uncertain significance202133238821332388Humanname
405667187CV3349697single nucleotide variantNM_012255.5(XRN2):c.887G>T (p.Cys296Phe)not specified [RCV004485724]uncertain significance202133357221333572Humanname
597804818CV3630547single nucleotide variantNM_012255.5(XRN2):c.527A>G (p.Tyr176Cys)not specified [RCV004882450]uncertain significance202133065621330656Humanname
597751830CV3630557single nucleotide variantNM_012255.5(XRN2):c.890C>T (p.Ala297Val)not specified [RCV004892829]uncertain significance202133357521333575Humanname
598195663CV3933817single nucleotide variantNM_012255.5(XRN2):c.547A>G (p.Asn183Asp)not specified [RCV005313370]uncertain significance202133067621330676Humanname
8628470CV83614single nucleotide variantNM_012255.3(XRN2):c.609A>C (p.Glu203Asp)Malignant melanoma [RCV000063695]not provided202133159321331593Humanname
156257974CV2322106single nucleotide variantNM_012255.5(XRN2):c.2134C>T (p.Pro712Ser)not specified [RCV004173848]uncertain significance202135660121356601Humanname
156361310CV2326477single nucleotide variantNM_012255.5(XRN2):c.1345C>T (p.Pro449Ser)not specified [RCV004183038]uncertain significance202134078721340787Humanname
156288631CV2327426single nucleotide variantNM_012255.5(XRN2):c.1084C>T (p.Arg362Cys)not specified [RCV004174847]uncertain significance202133395321333953Humanname
156077730CV2331903single nucleotide variantNM_012255.5(XRN2):c.1370C>T (p.Pro457Leu)not specified [RCV004186557]uncertain significance202134081221340812Humanname
155917565CV2332840single nucleotide variantNM_012255.5(XRN2):c.1514C>T (p.Pro505Leu)not specified [RCV004192104]uncertain significance202134419321344193Humanname
156163351CV2389562single nucleotide variantNM_012255.5(XRN2):c.1085G>A (p.Arg362His)not specified [RCV004243631]uncertain significance202133395421333954Humanname
156092816CV2389622single nucleotide variantNM_012255.5(XRN2):c.2221A>G (p.Met741Val)not specified [RCV004243680]uncertain significance202135775821357758Humanname
156007009CV2401264single nucleotide variantNM_012255.5(XRN2):c.1173G>C (p.Met391Ile)not specified [RCV004245813]uncertain significance202133412521334125Humanname
329368488CV2428037single nucleotide variantNM_012255.5(XRN2):c.1406A>G (p.Asn469Ser)not specified [RCV004254415]uncertain significance202134084821340848Humanname
329399171CV2436316single nucleotide variantNM_012255.5(XRN2):c.2170T>A (p.Leu724Met)not specified [RCV004251719]uncertain significance202135663721356637Humanname
329371912CV2454984single nucleotide variantNM_012255.5(XRN2):c.1772C>T (p.Pro591Leu)not specified [RCV004272249]uncertain significance202134825221348252Humanname
329371001CV2461912single nucleotide variantNM_012255.5(XRN2):c.2147A>G (p.His716Arg)not specified [RCV004271817]uncertain significance202135661421356614Humanname
401734229CV2690519single nucleotide variantNM_012255.5(XRN2):c.1364G>C (p.Ser455Thr)not specified [RCV004304638]uncertain significance202134080621340806Humanname
401885215CV2786710single nucleotide variantNM_012255.5(XRN2):c.2686A>T (p.Met896Leu)not specified [RCV004363830]uncertain significance202138690521386905Humanname
405667159CV3349691single nucleotide variantNM_012255.5(XRN2):c.1392G>A (p.Met464Ile)not specified [RCV004485718]uncertain significance202134083421340834Humanname
405667164CV3349692single nucleotide variantNM_012255.5(XRN2):c.1398G>A (p.Met466Ile)not specified [RCV004485719]uncertain significance202134084021340840Humanname
405667169CV3349693single nucleotide variantNM_012255.5(XRN2):c.1843C>T (p.Arg615Trp)not specified [RCV004485720]uncertain significance202134841021348410Humanname
405667173CV3349694single nucleotide variantNM_012255.5(XRN2):c.2407C>T (p.Arg803Cys)not specified [RCV004485721]uncertain significance202136565521365655Humanname
405667178CV3349695single nucleotide variantNM_012255.5(XRN2):c.2498A>G (p.Asn833Ser)not specified [RCV004485722]uncertain significance202136850421368504Humanname
407456185CV3493707single nucleotide variantNM_012255.5(XRN2):c.2666C>T (p.Pro889Leu)not specified [RCV004685856]uncertain significance202138688521386885Humanname
407456187CV3493708single nucleotide variantNM_012255.5(XRN2):c.2470A>G (p.Arg824Gly)not specified [RCV004685857]uncertain significance202136847621368476Humanname
407456190CV3493709single nucleotide variantNM_012255.5(XRN2):c.1098A>G (p.Ile366Met)not specified [RCV004685858]uncertain significance202133396721333967Humanname
407456195CV3493711single nucleotide variantNM_012255.5(XRN2):c.2009C>T (p.Thr670Ile)not specified [RCV004685860]uncertain significance202135486121354861Humanname
407456198CV3493712single nucleotide variantNM_012255.5(XRN2):c.1991A>G (p.Glu664Gly)not specified [RCV004685861]uncertain significance202135484321354843Humanname
597804816CV3630546single nucleotide variantNM_012255.5(XRN2):c.1433C>T (p.Thr478Met)not specified [RCV004882449]uncertain significance202134411221344112Humanname
597804820CV3630548single nucleotide variantNM_012255.5(XRN2):c.2153T>C (p.Ile718Thr)not specified [RCV004882451]uncertain significance202135662021356620Humanname
597804822CV3630549single nucleotide variantNM_012255.5(XRN2):c.1414C>T (p.Pro472Ser)not specified [RCV004882452]uncertain significance202134409321344093Humanname
597751808CV3630550single nucleotide variantNM_012255.5(XRN2):c.2413C>T (p.Arg805Trp)not specified [RCV004892825]uncertain significance202136566121365661Humanname
597804824CV3630551single nucleotide variantNM_012255.5(XRN2):c.1942G>T (p.Ala648Ser)not specified [RCV004882453]uncertain significance202135479421354794Humanname
597751813CV3630552single nucleotide variantNM_012255.5(XRN2):c.2578A>T (p.Met860Leu)not specified [RCV004892826]uncertain significance202136858421368584Humanname
597751819CV3630553single nucleotide variantNM_012255.5(XRN2):c.1924T>C (p.Tyr642His)not specified [RCV004892827]uncertain significance202134944921349449Humanname
597804826CV3630554single nucleotide variantNM_012255.5(XRN2):c.1844G>A (p.Arg615Gln)not specified [RCV004882454]uncertain significance202134841121348411Humanname
597751825CV3630555single nucleotide variantNM_012255.5(XRN2):c.1417T>G (p.Ser473Ala)not specified [RCV004892828]uncertain significance202134409621344096Humanname
597804827CV3630556single nucleotide variantNM_012255.5(XRN2):c.1121C>G (p.Thr374Ser)not specified [RCV004882455]uncertain significance202133399021333990Humanname
598241768CV3933818single nucleotide variantNM_012255.5(XRN2):c.1324G>C (p.Ala442Pro)not specified [RCV005296989]uncertain significance202134076621340766Humanname
598241772CV3933819single nucleotide variantNM_012255.5(XRN2):c.1474A>G (p.Ile492Val)not specified [RCV005296990]uncertain significance202134415321344153Humanname
598241778CV3933821single nucleotide variantNM_012255.5(XRN2):c.1423T>C (p.Ser475Pro)not specified [RCV005296991]uncertain significance202134410221344102Humanname
598195672CV3933822single nucleotide variantNM_012255.5(XRN2):c.1622C>T (p.Ser541Leu)not specified [RCV005313372]uncertain significance202134650721346507Humanname
598195677CV3933823single nucleotide variantNM_012255.5(XRN2):c.1856G>A (p.Ser619Asn)not specified [RCV005313373]uncertain significance202134842321348423Humanname
598195682CV3933824single nucleotide variantNM_012255.5(XRN2):c.2513C>T (p.Pro838Leu)not specified [RCV005313374]uncertain significance202136851921368519Humanname
598241782CV3933825single nucleotide variantNM_012255.5(XRN2):c.2765G>A (p.Arg922Gln)not specified [RCV005296992]uncertain significance202138698421386984Humanname
598195687CV3933826single nucleotide variantNM_012255.5(XRN2):c.2653G>T (p.Val885Phe)not specified [RCV005313375]uncertain significance202138687221386872Humanname
598241787CV3933827single nucleotide variantNM_012255.5(XRN2):c.2378G>A (p.Arg793Gln)not specified [RCV005296993]uncertain significance202136562621365626Humanname
15136283CV742288single nucleotide variantNM_012255.5(XRN2):c.1006G>A (p.Val336Ile)not provided [RCV000898603]benign202133377621333776Humanname