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Variants search result for All species
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29 records found for search term Nup35
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405680350CV3352423single nucleotide variantNM_138285.5(NUP35):c.26A>G (p.Gln9Arg)not specified [RCV004488556]uncertain significance2183124483183124483Humanname
329391621CV2448764single nucleotide variantNM_138285.5(NUP35):c.41G>T (p.Gly14Val)not specified [RCV004261461]uncertain significance2183128287183128287Humanname
597664434CV3570032single nucleotide variantNM_138285.5(NUP35):c.53T>C (p.Met18Thr)not specified [RCV004835448]uncertain significance2183128299183128299Humanname
156357322CV2318273single nucleotide variantNM_138285.5(NUP35):c.286G>A (p.Asp96Asn)not specified [RCV004179447]uncertain significance2183130492183130492Humanname
401888705CV2754750single nucleotide variantNM_138285.5(NUP35):c.291C>G (p.Asp97Glu)not specified [RCV004341238]uncertain significance2183130497183130497Humanname
405680346CV3352422single nucleotide variantNM_138285.5(NUP35):c.133G>A (p.Ala45Thr)not specified [RCV004488555]uncertain significance2183128379183128379Humanname
598235221CV4004798single nucleotide variantNM_138285.5(NUP35):c.137C>T (p.Pro46Leu)not specified [RCV005381978]uncertain significance2183128383183128383Humanname
598235229CV4004799single nucleotide variantNM_138285.5(NUP35):c.194G>C (p.Arg65Thr)not specified [RCV005381979]uncertain significance2183128440183128440Humanname
598235235CV4004800single nucleotide variantNM_138285.5(NUP35):c.238C>T (p.Pro80Ser)not specified [RCV005381980]uncertain significance2183130444183130444Humanname
156255218CV2194483single nucleotide variantNM_138285.5(NUP35):c.633G>A (p.Met211Ile)not specified [RCV004079576]uncertain significance2183158306183158306Humanname
155973342CV2224602single nucleotide variantNM_138285.5(NUP35):c.662C>T (p.Ala221Val)not specified [RCV004098170]uncertain significance2183158335183158335Humanname
155926260CV2258729single nucleotide variantNM_138285.5(NUP35):c.854C>T (p.Thr285Ile)not specified [RCV004117965]uncertain significance2183159603183159603Humanname
156156826CV2314408single nucleotide variantNM_138285.5(NUP35):c.824C>T (p.Thr275Ile)not specified [RCV004168525]uncertain significance2183159573183159573Humanname
155917808CV2332885single nucleotide variantNM_138285.5(NUP35):c.610A>G (p.Met204Val)not specified [RCV004192146]uncertain significance2183158283183158283Humanname
155918284CV2332972single nucleotide variantNM_138285.5(NUP35):c.734A>C (p.Asp245Ala)not specified [RCV004194273]uncertain significance2183158407183158407Humanname
155960980CV2390799single nucleotide variantNM_138285.5(NUP35):c.437G>A (p.Arg146Gln)not specified [RCV004241082]uncertain significance2183151547183151547Humanname
405680356CV3352424single nucleotide variantNM_138285.5(NUP35):c.400C>A (p.Gln134Lys)not specified [RCV004488557]uncertain significance2183151510183151510Humanname
405680361CV3352425single nucleotide variantNM_138285.5(NUP35):c.443C>T (p.Thr148Met)not specified [RCV004488558]uncertain significance2183151553183151553Humanname
405680367CV3352426single nucleotide variantNM_138285.5(NUP35):c.597C>G (p.Ile199Met)not specified [RCV004488559]uncertain significance2183157501183157501Humanname
405680371CV3352427single nucleotide variantNM_138285.5(NUP35):c.911C>T (p.Ser304Phe)not specified [RCV004488560]uncertain significance2183161061183161061Humanname
407522460CV3458969single nucleotide variantNM_138285.5(NUP35):c.371T>C (p.Val124Ala)not specified [RCV004652741]uncertain significance2183133597183133597Humanname
407477940CV3458970single nucleotide variantNM_138285.5(NUP35):c.952A>G (p.Lys318Glu)not specified [RCV004638897]uncertain significance2183161102183161102Humanname
597664409CV3570029single nucleotide variantNM_138285.5(NUP35):c.515A>G (p.Asp172Gly)not specified [RCV004835445]uncertain significance2183151625183151625Humanname
597664419CV3570030single nucleotide variantNM_138285.5(NUP35):c.640C>T (p.Arg214Cys)not specified [RCV004835446]uncertain significance2183158313183158313Humanname
597664428CV3570031single nucleotide variantNM_138285.5(NUP35):c.620C>T (p.Thr207Ile)not specified [RCV004835447]uncertain significance2183158293183158293Humanname
597664440CV3570033single nucleotide variantNM_138285.5(NUP35):c.370G>T (p.Val124Phe)not specified [RCV004835449]uncertain significance2183133596183133596Humanname
597643993CV3570034single nucleotide variantNM_138285.5(NUP35):c.692T>A (p.Ile231Asn)not specified [RCV004832722]uncertain significance2183158365183158365Humanname
597643999CV3570035single nucleotide variantNM_138285.5(NUP35):c.514G>A (p.Asp172Asn)not specified [RCV004832723]uncertain significance2183151624183151624Humanname
598266249CV4004801single nucleotide variantNM_138285.5(NUP35):c.463T>G (p.Leu155Val)not specified [RCV005388096]uncertain significance2183151573183151573Humanname