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67 records found for search term Pus7l
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597763565CV3582355single nucleotide variantNM_031292.5(PUS7L):c.41T>C (p.Leu14Ser)not specified [RCV004849568]uncertain significance124375520543755205Humanname
597763569CV3582356single nucleotide variantNM_031292.5(PUS7L):c.68T>C (p.Phe23Ser)not specified [RCV004849569]uncertain significance124375517843755178Humanname
597763576CV3582358single nucleotide variantNM_031292.5(PUS7L):c.86G>C (p.Ser29Thr)not specified [RCV004849571]uncertain significance124375516043755160Humanname
155925171CV2211758single nucleotide variantNM_031292.5(PUS7L):c.273G>C (p.Leu91Phe)not specified [RCV004086599]uncertain significance124375497343754973Humanname
156044675CV2268545single nucleotide variantNM_031292.5(PUS7L):c.232C>G (p.Leu78Val)not specified [RCV004123966]uncertain significance124375501443755014Humanname
155968409CV2339310single nucleotide variantNM_031292.5(PUS7L):c.151G>A (p.Asp51Asn)not specified [RCV004191543]likely benign124375509543755095Humanname
156383548CV2361598single nucleotide variantNM_031292.5(PUS7L):c.141T>G (p.Asn47Lys)not specified [RCV004221224]uncertain significance124375510543755105Humanname
329357189CV2431272single nucleotide variantNM_031292.5(PUS7L):c.250A>G (p.Arg84Gly)not specified [RCV004250606]uncertain significance124375499643754996Humanname
329386908CV2452672single nucleotide variantNM_031292.5(PUS7L):c.160A>T (p.Ile54Phe)not specified [RCV004275235]uncertain significance124375508643755086Humanname
401737330CV2699728single nucleotide variantNM_031292.5(PUS7L):c.251G>A (p.Arg84Lys)not specified [RCV004308068]uncertain significance124375499543754995Humanname
401717638CV2703941single nucleotide variantNM_031292.5(PUS7L):c.107T>C (p.Val36Ala)not specified [RCV004308839]uncertain significance124375513943755139Humanname
405658540CV3311705single nucleotide variantNM_031292.5(PUS7L):c.106G>A (p.Val36Ile)not specified [RCV004438217]uncertain significance124375514043755140Humanname
407473475CV3464789single nucleotide variantNM_031292.5(PUS7L):c.128G>T (p.Gly43Val)not specified [RCV004662758]uncertain significance124375511843755118Humanname
156132463CV2206607single nucleotide variantNM_031292.5(PUS7L):c.985C>T (p.Pro329Ser)not specified [RCV004080949]uncertain significance124374853543748535Humanname
156375598CV2210243single nucleotide variantNM_031292.5(PUS7L):c.859C>T (p.Arg287Cys)not specified [RCV004089409]uncertain significance124375438743754387Humanname
156333979CV2230848single nucleotide variantNM_031292.5(PUS7L):c.332T>C (p.Ile111Thr)not specified [RCV004092329]uncertain significance124375491443754914Humanname
156044693CV2268546single nucleotide variantNM_031292.5(PUS7L):c.786T>G (p.Phe262Leu)not specified [RCV004123967]uncertain significance124375446043754460Humanname
156253354CV2284044single nucleotide variantNM_031292.5(PUS7L):c.766C>T (p.Leu256Phe)not specified [RCV004144651]uncertain significance124375448043754480Humanname
156144629CV2292284single nucleotide variantNM_031292.5(PUS7L):c.356A>G (p.Glu119Gly)not specified [RCV004148317]uncertain significance124375489043754890Humanname
156204319CV2314128single nucleotide variantNM_031292.5(PUS7L):c.490G>A (p.Gly164Ser)not specified [RCV004166217]uncertain significance124375475643754756Humanname
156058658CV2316909single nucleotide variantNM_031292.5(PUS7L):c.673A>G (p.Lys225Glu)not specified [RCV004174426]uncertain significance124375457343754573Humanname
156048772CV2336469single nucleotide variantNM_031292.5(PUS7L):c.518C>A (p.Ala173Asp)not specified [RCV004194681]uncertain significance124375472843754728Humanname
156064331CV2340753single nucleotide variantNM_031292.5(PUS7L):c.923G>T (p.Arg308Leu)not specified [RCV004188115]uncertain significance124374859743748597Humanname
155938424CV2380744single nucleotide variantNM_031292.5(PUS7L):c.815C>T (p.Pro272Leu)not specified [RCV004218313]uncertain significance124375443143754431Humanname
156250198CV2394183single nucleotide variantNM_031292.5(PUS7L):c.334G>A (p.Val112Ile)not specified [RCV004236377]uncertain significance124375491243754912Humanname
401757965CV2708058single nucleotide variantNM_031292.5(PUS7L):c.707A>T (p.Asp236Val)not specified [RCV004309301]uncertain significance124375453943754539Humanname
401874613CV2781074single nucleotide variantNM_031292.5(PUS7L):c.965C>G (p.Ala322Gly)not specified [RCV004358453]uncertain significance124374855543748555Humanname
405658550CV3311709single nucleotide variantNM_031292.5(PUS7L):c.325G>A (p.Asp109Asn)not specified [RCV004438221]uncertain significance124375492143754921Humanname
405658552CV3311710single nucleotide variantNM_031292.5(PUS7L):c.404A>C (p.Glu135Ala)not specified [RCV004438222]uncertain significance124375484243754842Humanname
405658555CV3311711single nucleotide variantNM_031292.5(PUS7L):c.517G>A (p.Ala173Thr)not specified [RCV004438223]uncertain significance124375472943754729Humanname
405658558CV3311712single nucleotide variantNM_031292.5(PUS7L):c.542A>G (p.Gln181Arg)not specified [RCV004438224]uncertain significance124375470443754704Humanname
405658561CV3311713single nucleotide variantNM_031292.5(PUS7L):c.833T>G (p.Val278Gly)not specified [RCV004438225]uncertain significance124375441343754413Humanname
407499246CV3464787single nucleotide variantNM_031292.5(PUS7L):c.386T>C (p.Leu129Ser)not specified [RCV004669294]uncertain significance124375486043754860Humanname
598251086CV3901927single nucleotide variantNM_031292.5(PUS7L):c.967A>G (p.Ile323Val)not specified [RCV005259167]uncertain significance124374855343748553Humanname
598251091CV3901928single nucleotide variantNM_031292.5(PUS7L):c.772G>A (p.Glu258Lys)not specified [RCV005259168]uncertain significance124375447443754474Humanname
598251114CV3901933single nucleotide variantNM_031292.5(PUS7L):c.373T>G (p.Leu125Val)not specified [RCV005259173]uncertain significance124375487343754873Humanname
156331480CV2218168single nucleotide variantNM_031292.5(PUS7L):c.1649A>G (p.Tyr550Cys)not specified [RCV004086589]uncertain significance124373645743736457Humanname
156233657CV2227783single nucleotide variantNM_031292.5(PUS7L):c.2044G>A (p.Asp682Asn)not specified [RCV004094165]uncertain significance124373043843730438Humanname
156301854CV2241685single nucleotide variantNM_031292.5(PUS7L):c.1269A>T (p.Lys423Asn)not specified [RCV004106630]uncertain significance124374255043742550Humanname
156054043CV2243034single nucleotide variantNM_031292.5(PUS7L):c.1517A>C (p.His506Pro)not specified [RCV004109953]uncertain significance124373658943736589Humanname
156266221CV2247140single nucleotide variantNM_031292.5(PUS7L):c.1922A>G (p.Tyr641Cys)not specified [RCV004114671]uncertain significance124373056043730560Humanname
156097656CV2253207single nucleotide variantNM_031292.5(PUS7L):c.1636A>G (p.Arg546Gly)not specified [RCV004599489]uncertain significance124373647043736470Humanname
155958692CV2282239single nucleotide variantNM_031292.5(PUS7L):c.2047C>T (p.Leu683Phe)not specified [RCV004132814]uncertain significance124373043543730435Humanname
155952627CV2306157single nucleotide variantNM_031292.5(PUS7L):c.1291C>T (p.Pro431Ser)not specified [RCV004162907]uncertain significance124374252843742528Humanname
156173025CV2317080single nucleotide variantNM_031292.5(PUS7L):c.1576A>G (p.Met526Val)not specified [RCV004174565]uncertain significance124373653043736530Humanname
155979079CV2335286single nucleotide variantNM_031292.5(PUS7L):c.1453A>G (p.Lys485Glu)not specified [RCV004186852]uncertain significance124373665343736653Humanname
155975030CV2342621single nucleotide variantNM_031292.5(PUS7L):c.1777C>G (p.Gln593Glu)not specified [RCV004196709]uncertain significance124373170743731707Humanname
156074788CV2365551single nucleotide variantNM_031292.5(PUS7L):c.1578G>A (p.Met526Ile)not specified [RCV004211665]uncertain significance124373652843736528Humanname
156172205CV2380788single nucleotide variantNM_031292.5(PUS7L):c.1829T>A (p.Val610Glu)not specified [RCV004218350]uncertain significance124373065343730653Humanname
156082557CV2384863single nucleotide variantNM_031292.5(PUS7L):c.1891C>T (p.Pro631Ser)not specified [RCV004225741]uncertain significance124373059143730591Humanname
329373245CV2434157single nucleotide variantNM_031292.5(PUS7L):c.1540G>A (p.Gly514Ser)not specified [RCV004250053]uncertain significance124373656643736566Humanname
329376537CV2472142single nucleotide variantNM_031292.5(PUS7L):c.1283A>T (p.Tyr428Phe)not specified [RCV004283270]uncertain significance124374253643742536Humanname
401731589CV2712056single nucleotide variantNM_031292.5(PUS7L):c.1721G>A (p.Ser574Asn)not specified [RCV004311796]uncertain significance124373638543736385Humanname
401900089CV2780392single nucleotide variantNM_031292.5(PUS7L):c.1519C>T (p.Arg507Cys)not specified [RCV004357790]uncertain significance124373658743736587Humanname
405658543CV3311706single nucleotide variantNM_031292.5(PUS7L):c.1097A>T (p.Glu366Val)not specified [RCV004438218]uncertain significance124374621243746212Humanname
405658547CV3311708single nucleotide variantNM_031292.5(PUS7L):c.1939C>T (p.His647Tyr)not specified [RCV004438220]uncertain significance124373054343730543Humanname
407473471CV3464788single nucleotide variantNM_031292.5(PUS7L):c.1584A>G (p.Ile528Met)not specified [RCV004662757]uncertain significance124373652243736522Humanname
597763553CV3582352single nucleotide variantNM_031292.5(PUS7L):c.1631C>T (p.Ser544Phe)not specified [RCV004849565]uncertain significance124373647543736475Humanname
597763557CV3582353single nucleotide variantNM_031292.5(PUS7L):c.2101G>A (p.Val701Ile)not specified [RCV004849566]uncertain significance124373038143730381Humanname
597763561CV3582354single nucleotide variantNM_031292.5(PUS7L):c.1412T>C (p.Val471Ala)not specified [RCV004849567]uncertain significance124373834243738342Humanname
597763572CV3582357single nucleotide variantNM_031292.5(PUS7L):c.1235G>T (p.Arg412Ile)not specified [RCV004849570]uncertain significance124374607443746074Humanname
597763580CV3582359single nucleotide variantNM_031292.5(PUS7L):c.1430A>G (p.Tyr477Cys)not specified [RCV004849572]uncertain significance124373832443738324Humanname
597763588CV3582361single nucleotide variantNM_031292.5(PUS7L):c.1312A>T (p.Arg438Trp)not specified [RCV004849574]uncertain significance124374250743742507Humanname
598251095CV3901929single nucleotide variantNM_031292.5(PUS7L):c.1577T>C (p.Met526Thr)not specified [RCV005259169]uncertain significance124373652943736529Humanname
598251100CV3901930single nucleotide variantNM_031292.5(PUS7L):c.1279A>G (p.Asn427Asp)not specified [RCV005259170]uncertain significance124374254043742540Humanname
598251109CV3901932single nucleotide variantNM_031292.5(PUS7L):c.1810C>G (p.Gln604Glu)not specified [RCV005259172]uncertain significance124373067243730672Humanname
598251118CV3901934single nucleotide variantNM_031292.5(PUS7L):c.1996A>G (p.Lys666Glu)not specified [RCV005259174]likely benign124373048643730486Humanname