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Variants search result for Homo sapiens
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36 records found for search term Cdc42ep5
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
598167686CV3947122single nucleotide variantNM_145057.4(CDC42EP5):c.22G>A (p.Gly8Ser)not specified [RCV005308105]uncertain significance195446552654465526Humanname
155954135CV2379147single nucleotide variantNM_145057.4(CDC42EP5):c.71C>G (p.Ser24Cys)not specified [RCV004235939]uncertain significance195446547754465477Humanname
597788123CV3644907single nucleotide variantNM_145057.4(CDC42EP5):c.92G>A (p.Arg31Gln)not specified [RCV004901399]uncertain significance195446545654465456Humanname
156219606CV2225969single nucleotide variantNM_145057.4(CDC42EP5):c.215C>T (p.Pro72Leu)not specified [RCV004105134]uncertain significance195446533354465333Humanname
156314810CV2253317single nucleotide variantNM_145057.4(CDC42EP5):c.229C>T (p.Pro77Ser)not specified [RCV004123150]uncertain significance195446531954465319Humanname
156333165CV2270531single nucleotide variantNM_145057.4(CDC42EP5):c.260C>A (p.Pro87Gln)not specified [RCV004137488]uncertain significance195446528854465288Humanname
155994831CV2379596single nucleotide variantNM_145057.4(CDC42EP5):c.277C>G (p.Leu93Val)not specified [RCV004217296]uncertain significance195446527154465271Humanname
329383870CV2434900single nucleotide variantNM_145057.4(CDC42EP5):c.230C>T (p.Pro77Leu)not specified [RCV004250774]uncertain significance195446531854465318Humanname
401779025CV2733064single nucleotide variantNM_145057.4(CDC42EP5):c.188C>A (p.Pro63His)not specified [RCV004331998]uncertain significance195446536054465360Humanname
401869344CV2772367single nucleotide variantNM_145057.4(CDC42EP5):c.199G>A (p.Ala67Thr)not specified [RCV004353377]uncertain significance195446534954465349Humanname
405774266CV3296262single nucleotide variantNM_145057.4(CDC42EP5):c.103C>T (p.His35Tyr)not specified [RCV004435827]uncertain significance195446544554465445Humanname
405774272CV3296263single nucleotide variantNM_145057.4(CDC42EP5):c.140C>T (p.Ser47Leu)not specified [RCV004435828]uncertain significance195446540854465408Humanname
405774280CV3296264single nucleotide variantNM_145057.4(CDC42EP5):c.142T>C (p.Phe48Leu)not specified [RCV004435829]uncertain significance195446540654465406Humanname
405774284CV3296265single nucleotide variantNM_145057.4(CDC42EP5):c.200C>A (p.Ala67Asp)not specified [RCV004435830]uncertain significance195446534854465348Humanname
407454738CV3425163single nucleotide variantNM_145057.4(CDC42EP5):c.184G>A (p.Ala62Thr)not specified [RCV004609966]uncertain significance195446536454465364Humanname
407498756CV3425164single nucleotide variantNM_145057.4(CDC42EP5):c.290C>T (p.Pro97Leu)not specified [RCV004606725]uncertain significance195446525854465258Humanname
597788127CV3644908single nucleotide variantNM_145057.4(CDC42EP5):c.200C>G (p.Ala67Gly)not specified [RCV004901400]uncertain significance195446534854465348Humanname
597788134CV3644910single nucleotide variantNM_145057.4(CDC42EP5):c.169C>T (p.Pro57Ser)not specified [RCV004901402]uncertain significance195446537954465379Humanname
598229405CV3951061single nucleotide variantNM_145057.4(CDC42EP5):c.150C>G (p.Ser50Arg)not specified [RCV005319218]uncertain significance195446539854465398Humanname
598167674CV3951063single nucleotide variantNM_145057.4(CDC42EP5):c.224C>G (p.Ala75Gly)not specified [RCV005308103]uncertain significance195446532454465324Humanname
598167680CV3951064single nucleotide variantNM_145057.4(CDC42EP5):c.206G>A (p.Arg69His)not specified [RCV005308104]uncertain significance195446534254465342Humanname
155931251CV2220999single nucleotide variantNM_145057.4(CDC42EP5):c.442C>G (p.Leu148Val)not specified [RCV004092684]uncertain significance195446510654465106Humanname
155980381CV2263648single nucleotide variantNM_145057.4(CDC42EP5):c.439G>A (p.Gly147Ser)not specified [RCV004135649]uncertain significance195446510954465109Humanname
156152594CV2307646single nucleotide variantNM_145057.4(CDC42EP5):c.386C>G (p.Pro129Arg)not specified [RCV004168063]uncertain significance195446516254465162Humanname
155976262CV2338579single nucleotide variantNM_145057.4(CDC42EP5):c.370C>T (p.Arg124Cys)not specified [RCV004182172]uncertain significance195446517854465178Humanname
156146370CV2397414single nucleotide variantNM_145057.4(CDC42EP5):c.362C>T (p.Ala121Val)not specified [RCV004238933]uncertain significance195446518654465186Humanname
329369385CV2424807single nucleotide variantNM_145057.4(CDC42EP5):c.391C>A (p.Gln131Lys)not specified [RCV004248696]likely benign195446515754465157Humanname
401767421CV2729648single nucleotide variantNM_145057.4(CDC42EP5):c.434T>G (p.Val145Gly)not specified [RCV004331910]uncertain significance195446511454465114Humanname
401887753CV2770409single nucleotide variantNM_145057.4(CDC42EP5):c.409A>C (p.Asn137His)not specified [RCV004358055]uncertain significance195446513954465139Humanname
401892347CV2777475single nucleotide variantNM_145057.4(CDC42EP5):c.346G>A (p.Ala116Thr)not specified [RCV004356246]uncertain significance195446520254465202Humanname
405774290CV3296266single nucleotide variantNM_145057.4(CDC42EP5):c.354G>C (p.Lys118Asn)not specified [RCV004435831]uncertain significance195446519454465194Humanname
405774296CV3296267single nucleotide variantNM_145057.4(CDC42EP5):c.368C>G (p.Pro123Arg)not specified [RCV004435832]uncertain significance195446518054465180Humanname
405774302CV3296268single nucleotide variantNM_145057.4(CDC42EP5):c.398G>A (p.Arg133His)not specified [RCV004435833]uncertain significance195446515054465150Humanname
597788131CV3644909single nucleotide variantNM_145057.4(CDC42EP5):c.377G>C (p.Gly126Ala)not specified [RCV004901401]uncertain significance195446517154465171Humanname
598167657CV3951059single nucleotide variantNM_145057.4(CDC42EP5):c.316G>C (p.Val106Leu)not specified [RCV005308100]uncertain significance195446523254465232Humanname
598167662CV3951060single nucleotide variantNM_145057.4(CDC42EP5):c.395C>A (p.Ala132Asp)not specified [RCV005308101]uncertain significance195446515354465153Humanname