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Variants search result for Homo sapiens
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49 records found for search term Cxxc1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15185751CV778358single nucleotide variantNM_014593.4(CXXC1):c.122+9G>Anot provided [RCV000953075]benign185028673150286731Humanname
13827760CV578561single nucleotide variantNM_014593.4(CXXC1):c.1574+1G>Cnot provided [RCV000714772]uncertain significance185028351450283514Humanname
150505998CV1213668single nucleotide variantNM_014593.4(CXXC1):c.1413+13G>Cnot provided [RCV001595924]benign185028388150283881Humanname
15179574CV727748single nucleotide variantNM_014593.4(CXXC1):c.27G>A (p.Glu9=)not provided [RCV000885322]benign185028683550286835Humanname
156231220CV2235128single nucleotide variantNM_014593.4(CXXC1):c.4G>A (p.Glu2Lys)not specified [RCV004106870]uncertain significance185028685850286858Humanname
15115678CV741400single nucleotide variantNM_014593.4(CXXC1):c.75G>T (p.Ala25=)not provided [RCV000895070]likely benign185028678750286787Humanname
405853075CV3393506single nucleotide variantNM_014593.4(CXXC1):c.345T>C (p.Asp115=)not provided [RCV004546236]likely benign185028613650286136Humanname
15150791CV727747single nucleotide variantNM_014593.4(CXXC1):c.681G>A (p.Thr227=)not provided [RCV000879458]benign185028523350285233Humanname
15153393CV741399single nucleotide variantNM_014593.4(CXXC1):c.627G>A (p.Gln209=)not provided [RCV000901752]benign185028576150285761Humanname
150439092CV1266725single nucleotide variantNM_014593.4(CXXC1):c.1326T>C (p.Thr442=)not provided [RCV001690160]benign185028398150283981Humanname
156184816CV2294902single nucleotide variantNM_014593.4(CXXC1):c.254G>A (p.Arg85Gln)not specified [RCV004156054]uncertain significance185028622750286227Humanname
156260611CV2322313single nucleotide variantNM_014593.4(CXXC1):c.159C>A (p.Asp53Glu)not specified [RCV004176073]uncertain significance185028660350286603Humanname
401863015CV2775542single nucleotide variantNM_014593.4(CXXC1):c.221G>A (p.Arg74Lys)not specified [RCV004350713]uncertain significance185028654150286541Humanname
405665810CV3243268single nucleotide variantNM_014593.4(CXXC1):c.247C>G (p.Arg83Gly)not specified [RCV004367621]uncertain significance185028623450286234Humanname
597656121CV3657935single nucleotide variantNM_014593.4(CXXC1):c.268C>T (p.Arg90Trp)not specified [RCV004911063]uncertain significance185028621350286213Humanname
15186916CV727746single nucleotide variantNM_014593.4(CXXC1):c.1596T>C (p.Asp532=)not provided [RCV000887109]benign185028334050283340Humanname
155969113CV2213275single nucleotide variantNM_014593.4(CXXC1):c.362G>A (p.Arg121Gln)not specified [RCV004085493]uncertain significance185028611950286119Humanname
155977384CV2246834single nucleotide variantNM_014593.4(CXXC1):c.673C>A (p.Pro225Thr)not specified [RCV004112650]uncertain significance185028524150285241Humanname
155949580CV2267682single nucleotide variantNM_014593.4(CXXC1):c.709C>T (p.Arg237Trp)not specified [RCV004134229]uncertain significance185028520550285205Humanname
156165049CV2270311single nucleotide variantNM_014593.4(CXXC1):c.325C>T (p.Arg109Cys)not specified [RCV004135522]uncertain significance185028615650286156Humanname
155904788CV2276139single nucleotide variantNM_014593.4(CXXC1):c.665C>T (p.Ser222Leu)not specified [RCV004141802]uncertain significance185028532650285326Humanname
156008356CV2299860single nucleotide variantNM_014593.4(CXXC1):c.301G>A (p.Glu101Lys)not specified [RCV004149003]uncertain significance185028618050286180Humanname
156149327CV2307403single nucleotide variantNM_014593.4(CXXC1):c.901G>T (p.Asp301Tyr)not specified [RCV004166081]uncertain significance185028501350285013Humanname
155928502CV2363297single nucleotide variantNM_014593.4(CXXC1):c.398C>T (p.Ala133Val)not specified [RCV004213849]uncertain significance185028608350286083Humanname
329373735CV2452635single nucleotide variantNM_014593.4(CXXC1):c.689A>G (p.Glu230Gly)not specified [RCV004275207]uncertain significance185028522550285225Humanname
401735862CV2672760single nucleotide variantNM_014593.4(CXXC1):c.326G>A (p.Arg109His)not specified [RCV004287770]uncertain significance185028615550286155Humanname
405665823CV3243270single nucleotide variantNM_014593.4(CXXC1):c.439T>G (p.Leu147Val)not specified [RCV004367623]uncertain significance185028604250286042Humanname
405665828CV3243271single nucleotide variantNM_014593.4(CXXC1):c.803A>C (p.Glu268Ala)not specified [RCV004367624]uncertain significance185028511150285111Humanname
405665833CV3243272single nucleotide variantNM_014593.4(CXXC1):c.955G>A (p.Ala319Thr)not specified [RCV004367625]uncertain significance185028479750284797Humanname
597656112CV3657936single nucleotide variantNM_014593.4(CXXC1):c.820G>A (p.Ala274Thr)not specified [RCV004911064]uncertain significance185028509450285094Humanname
597656093CV3657939single nucleotide variantNM_014593.4(CXXC1):c.853C>T (p.Pro285Ser)not specified [RCV004911067]uncertain significance185028506150285061Humanname
597656077CV3657941single nucleotide variantNM_014593.4(CXXC1):c.553G>A (p.Asp185Asn)not specified [RCV004911069]uncertain significance185028583550285835Humanname
597656068CV3657942single nucleotide variantNM_014593.4(CXXC1):c.773A>C (p.Glu258Ala)not specified [RCV004911070]uncertain significance185028514150285141Humanname
598236765CV3956203single nucleotide variantNM_014593.4(CXXC1):c.346C>T (p.Pro116Ser)not specified [RCV005320502]uncertain significance185028613550286135Humanname
598236778CV3956206single nucleotide variantNM_014593.4(CXXC1):c.710G>A (p.Arg237Gln)not specified [RCV005320505]uncertain significance185028520450285204Humanname
617151541CV4021850single nucleotide variantNM_014593.4(CXXC1):c.611G>A (p.Arg204Gln)not provided [RCV005426811]uncertain significance185028577750285777Humanname
156316648CV2250937single nucleotide variantNM_014593.4(CXXC1):c.1958G>T (p.Ser653Ile)not specified [RCV004123517]uncertain significance185028260650282606Humanname
156277961CV2252044single nucleotide variantNM_014593.4(CXXC1):c.1330C>G (p.Leu444Val)not specified [RCV004122079]uncertain significance185028397750283977Humanname
156148022CV2394460single nucleotide variantNM_014593.4(CXXC1):c.1538C>T (p.Thr513Met)not specified [RCV004240827]uncertain significance185028355150283551Humanname
401882391CV2774829single nucleotide variantNM_014593.4(CXXC1):c.1315A>G (p.Ser439Gly)not specified [RCV004343917]uncertain significance185028399250283992Humanname
405665791CV3243264single nucleotide variantNM_014593.4(CXXC1):c.1042C>T (p.His348Tyr)not specified [RCV004367617]uncertain significance185028454150284541Humanname
405665796CV3243265single nucleotide variantNM_014593.4(CXXC1):c.1142T>C (p.Val381Ala)not specified [RCV004367618]uncertain significance185028444150284441Humanname
405665801CV3243266single nucleotide variantNM_014593.4(CXXC1):c.1190T>G (p.Met397Arg)not specified [RCV004367619]uncertain significance185028439350284393Humanname
405665806CV3243267single nucleotide variantNM_014593.4(CXXC1):c.1932T>A (p.Asp644Glu)not specified [RCV004367620]uncertain significance185028263250282632Humanname
597656107CV3657937single nucleotide variantNM_014593.4(CXXC1):c.1150G>A (p.Ala384Thr)not specified [RCV004911065]uncertain significance185028443350284433Humanname
597656100CV3657938single nucleotide variantNM_014593.4(CXXC1):c.1025A>C (p.Glu342Ala)not specified [RCV004911066]uncertain significance185028455850284558Humanname
597656059CV3657943single nucleotide variantNM_014593.4(CXXC1):c.1526A>T (p.Tyr509Phe)not specified [RCV004911071]uncertain significance185028356350283563Humanname
598236769CV3956204single nucleotide variantNM_014593.4(CXXC1):c.1400G>A (p.Arg467His)not specified [RCV005320503]uncertain significance185028390750283907Humanname
598236773CV3956205single nucleotide variantNM_014593.4(CXXC1):c.1345C>T (p.Arg449Cys)not specified [RCV005320504]uncertain significance185028396250283962Humanname