Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.134887244_134887246delinsTGCCA1883419546FCN2c.771_773delinsTGC (p.Cys257=)
c.657_659delinsTGC (p.Cys219=)
c.624_626delinsTGC (p.Cys208=)
c.738_740delinsTGC (p.Cys246=)
9g.134887245G>ACA375461532FCN2c.772G>A (p.Ala258Thr)
c.658G>A (p.Ala220Thr)
c.625G>A (p.Ala209Thr)
c.739G>A (p.Ala247Thr)
9g.134887245G>CCA5321362FCN2c.772G>C (p.Ala258Pro)
c.658G>C (p.Ala220Pro)
c.625G>C (p.Ala209Pro)
c.739G>C (p.Ala247Pro)
 dbSNP ExAC
9g.134887245G=CA1883419547FCN2c.772G= (p.Ala258=)
c.658G= (p.Ala220=)
c.625G= (p.Ala209=)
c.739G= (p.Ala247=)
9g.134887245G>TCA5321361FCN2c.772G>T (p.Ala258Ser)
c.658G>T (p.Ala220Ser)
c.625G>T (p.Ala209Ser)
c.739G>T (p.Ala247Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
9g.134887245_134887246delCA591363722FCN2c.772_773del (p.Ala258CysfsTer?)
c.658_659del (p.Ala220CysfsTer?)
c.625_626del (p.Ala209CysfsTer?)
c.739_740del (p.Ala247CysfsTer?)
 dbSNP gnomAD v2 gnomAD v4
9g.134887246C>ACA375461533FCN2c.773C>A (p.Ala258Asp)
c.659C>A (p.Ala220Asp)
c.626C>A (p.Ala209Asp)
c.740C>A (p.Ala247Asp)
9g.134887246C>GCA375461534FCN2c.773C>G (p.Ala258Gly)
c.659C>G (p.Ala220Gly)
c.626C>G (p.Ala209Gly)
c.740C>G (p.Ala247Gly)
9g.134887246C>TCA375461535FCN2c.773C>T (p.Ala258Val)
c.659C>T (p.Ala220Val)
c.626C>T (p.Ala209Val)
c.740C>T (p.Ala247Val)
9g.134887247T>ACA467816397FCN2c.774T>A (p.Ala258=)
c.660T>A (p.Ala220=)
c.627T>A (p.Ala209=)
c.741T>A (p.Ala247=)
9g.134887247T>CCA5321363FCN2c.774T>C (p.Ala258=)
c.660T>C (p.Ala220=)
c.627T>C (p.Ala209=)
c.741T>C (p.Ala247=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.134887247T>GCA467816394FCN2c.774T>G (p.Ala258=)
c.660T>G (p.Ala220=)
c.627T>G (p.Ala209=)
c.741T>G (p.Ala247=)
9g.134887247T=CA1883419548FCN2c.774T= (p.Ala258=)
c.660T= (p.Ala220=)
c.627T= (p.Ala209=)
c.741T= (p.Ala247=)
9g.134887248G>ACA375461536FCN2c.775G>A (p.Val259Met)
c.661G>A (p.Val221Met)
c.628G>A (p.Val210Met)
c.742G>A (p.Val248Met)
 gnomAD v4
9g.134887248G>CCA375461537FCN2c.775G>C (p.Val259Leu)
c.661G>C (p.Val221Leu)
c.628G>C (p.Val210Leu)
c.742G>C (p.Val248Leu)
 dbSNP gnomAD v2 gnomAD v4
9g.134887248G=CA1883419549FCN2c.775G= (p.Val259=)
c.661G= (p.Val221=)
c.628G= (p.Val210=)
c.742G= (p.Val248=)
9g.134887248G>TCA375461538FCN2c.775G>T (p.Val259Leu)
c.661G>T (p.Val221Leu)
c.628G>T (p.Val210Leu)
c.742G>T (p.Val248Leu)
 dbSNP
9g.134887249T>ACA375461541FCN2c.776T>A (p.Val259Glu)
c.662T>A (p.Val221Glu)
c.629T>A (p.Val210Glu)
c.743T>A (p.Val248Glu)
9g.134887249T>CCA375461540FCN2c.776T>C (p.Val259Ala)
c.662T>C (p.Val221Ala)
c.629T>C (p.Val210Ala)
c.743T>C (p.Val248Ala)
 gnomAD v4
9g.134887249T>GCA375461539FCN2c.776T>G (p.Val259Gly)
c.662T>G (p.Val221Gly)
c.629T>G (p.Val210Gly)
c.743T>G (p.Val248Gly)
9g.134887250G>ACA467816399FCN2c.777G>A (p.Val259=)
c.663G>A (p.Val221=)
c.630G>A (p.Val210=)
c.744G>A (p.Val248=)
9g.134887250G>CCA467816401FCN2c.777G>C (p.Val259=)
c.663G>C (p.Val221=)
c.630G>C (p.Val210=)
c.744G>C (p.Val248=)
9g.134887250G>TCA467816402FCN2c.777G>T (p.Val259=)
c.663G>T (p.Val221=)
c.630G>T (p.Val210=)
c.744G>T (p.Val248=)
9g.134887251A=CA1883419550FCN2c.778A= (p.Met260=)
c.664A= (p.Met222=)
c.631A= (p.Met211=)
c.745A= (p.Met249=)
9g.134887251A>CCA375461542FCN2c.778A>C (p.Met260Leu)
c.664A>C (p.Met222Leu)
c.631A>C (p.Met211Leu)
c.745A>C (p.Met249Leu)
 gnomAD v4
9g.134887251A>GCA375461543FCN2c.778A>G (p.Met260Val)
c.664A>G (p.Met222Val)
c.631A>G (p.Met211Val)
c.745A>G (p.Met249Val)
9g.134887251A>TCA5321364FCN2c.778A>T (p.Met260Leu)
c.664A>T (p.Met222Leu)
c.631A>T (p.Met211Leu)
c.745A>T (p.Met249Leu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.134887252T>ACA375461544FCN2c.779T>A (p.Met260Lys)
c.665T>A (p.Met222Lys)
c.632T>A (p.Met211Lys)
c.746T>A (p.Met249Lys)
9g.134887252T>CCA375461545FCN2c.779T>C (p.Met260Thr)
c.665T>C (p.Met222Thr)
c.632T>C (p.Met211Thr)
c.746T>C (p.Met249Thr)
 gnomAD v4 COSMIC
9g.134887252T>GCA375461546FCN2c.779T>G (p.Met260Arg)
c.665T>G (p.Met222Arg)
c.632T>G (p.Met211Arg)
c.746T>G (p.Met249Arg)
9g.134887253G>ACA375461547FCN2c.780G>A (p.Met260Ile)
c.666G>A (p.Met222Ile)
c.633G>A (p.Met211Ile)
c.747G>A (p.Met249Ile)
 gnomAD v4 COSMIC
9g.134887253G>CCA375461548FCN2c.780G>C (p.Met260Ile)
c.666G>C (p.Met222Ile)
c.633G>C (p.Met211Ile)
c.747G>C (p.Met249Ile)
9g.134887253G>TCA375461549FCN2c.780G>T (p.Met260Ile)
c.666G>T (p.Met222Ile)
c.633G>T (p.Met211Ile)
c.747G>T (p.Met249Ile)
9g.134887254T>ACA375461550FCN2c.781T>A (p.Phe261Ile)
c.667T>A (p.Phe223Ile)
c.634T>A (p.Phe212Ile)
c.748T>A (p.Phe250Ile)
9g.134887254T>CCA375461551FCN2c.781T>C (p.Phe261Leu)
c.667T>C (p.Phe223Leu)
c.634T>C (p.Phe212Leu)
c.748T>C (p.Phe250Leu)
9g.134887254T>GCA375461552FCN2c.781T>G (p.Phe261Val)
c.667T>G (p.Phe223Val)
c.634T>G (p.Phe212Val)
c.748T>G (p.Phe250Val)
9g.134887255T>ACA375461553FCN2c.782T>A (p.Phe261Tyr)
c.668T>A (p.Phe223Tyr)
c.635T>A (p.Phe212Tyr)
c.749T>A (p.Phe250Tyr)
9g.134887255T>CCA375461555FCN2c.782T>C (p.Phe261Ser)
c.668T>C (p.Phe223Ser)
c.635T>C (p.Phe212Ser)
c.749T>C (p.Phe250Ser)
9g.134887255T>GCA375461554FCN2c.782T>G (p.Phe261Cys)
c.668T>G (p.Phe223Cys)
c.635T>G (p.Phe212Cys)
c.749T>G (p.Phe250Cys)
9g.134887256T>ACA375461556FCN2c.783T>A (p.Phe261Leu)
c.669T>A (p.Phe223Leu)
c.636T>A (p.Phe212Leu)
c.750T>A (p.Phe250Leu)
9g.134887256T>CCA467816406FCN2c.783T>C (p.Phe261=)
c.669T>C (p.Phe223=)
c.636T>C (p.Phe212=)
c.750T>C (p.Phe250=)
9g.134887256T>GCA375461557FCN2c.783T>G (p.Phe261Leu)
c.669T>G (p.Phe223Leu)
c.636T>G (p.Phe212Leu)
c.750T>G (p.Phe250Leu)
9g.134887257C>ACA375461558FCN2c.784C>A (p.Gln262Lys)
c.670C>A (p.Gln224Lys)
c.637C>A (p.Gln213Lys)
c.751C>A (p.Gln251Lys)
9g.134887257C>GCA375461559FCN2c.784C>G (p.Gln262Glu)
c.670C>G (p.Gln224Glu)
c.637C>G (p.Gln213Glu)
c.751C>G (p.Gln251Glu)
9g.134887257C>TCA375461560FCN2c.784C>T (p.Gln262Ter)
c.670C>T (p.Gln224Ter)
c.637C>T (p.Gln213Ter)
c.751C>T (p.Gln251Ter)
9g.134887258A>CCA375461561FCN2c.785A>C (p.Gln262Pro)
c.671A>C (p.Gln224Pro)
c.638A>C (p.Gln213Pro)
c.752A>C (p.Gln251Pro)
9g.134887258A>GCA375461562FCN2c.785A>G (p.Gln262Arg)
c.671A>G (p.Gln224Arg)
c.638A>G (p.Gln213Arg)
c.752A>G (p.Gln251Arg)
9g.134887258A>TCA375461563FCN2c.785A>T (p.Gln262Leu)
c.671A>T (p.Gln224Leu)
c.638A>T (p.Gln213Leu)
c.752A>T (p.Gln251Leu)
9g.134887259G>ACA467816409FCN2c.786G>A (p.Gln262=)
c.672G>A (p.Gln224=)
c.639G>A (p.Gln213=)
c.753G>A (p.Gln251=)
 gnomAD v4
9g.134887259G>CCA375461565FCN2c.786G>C (p.Gln262His)
c.672G>C (p.Gln224His)
c.639G>C (p.Gln213His)
c.753G>C (p.Gln251His)
9g.134887259G>TCA375461564FCN2c.786G>T (p.Gln262His)
c.672G>T (p.Gln224His)
c.639G>T (p.Gln213His)
c.753G>T (p.Gln251His)
9g.134887260G>ACA375461566FCN2c.787G>A (p.Gly263Arg)
c.673G>A (p.Gly225Arg)
c.640G>A (p.Gly214Arg)
c.754G>A (p.Gly252Arg)
 dbSNP gnomAD v2 gnomAD v4
9g.134887260G>CCA375461567FCN2c.787G>C (p.Gly263Arg)
c.673G>C (p.Gly225Arg)
c.640G>C (p.Gly214Arg)
c.754G>C (p.Gly252Arg)
 gnomAD v4
9g.134887260G=CA1883419551FCN2c.787G= (p.Gly263=)
c.673G= (p.Gly225=)
c.640G= (p.Gly214=)
c.754G= (p.Gly252=)
9g.134887260G>TCA375461568FCN2c.787G>T (p.Gly263Ter)
c.673G>T (p.Gly225Ter)
c.640G>T (p.Gly214Ter)
c.754G>T (p.Gly252Ter)
9g.134887261G>ACA375461569FCN2c.788G>A (p.Gly263Glu)
c.674G>A (p.Gly225Glu)
c.641G>A (p.Gly214Glu)
c.755G>A (p.Gly252Glu)
9g.134887261G>CCA375461570FCN2c.788G>C (p.Gly263Ala)
c.674G>C (p.Gly225Ala)
c.641G>C (p.Gly214Ala)
c.755G>C (p.Gly252Ala)
9g.134887261G>TCA375461571FCN2c.788G>T (p.Gly263Val)
c.674G>T (p.Gly225Val)
c.641G>T (p.Gly214Val)
c.755G>T (p.Gly252Val)
9g.134887262A>CCA467816412FCN2c.789A>C (p.Gly263=)
c.675A>C (p.Gly225=)
c.642A>C (p.Gly214=)
c.756A>C (p.Gly252=)
9g.134887262A>GCA467816413FCN2c.789A>G (p.Gly263=)
c.675A>G (p.Gly225=)
c.642A>G (p.Gly214=)
c.756A>G (p.Gly252=)
9g.134887262A>TCA467816415FCN2c.789A>T (p.Gly263=)
c.675A>T (p.Gly225=)
c.642A>T (p.Gly214=)
c.756A>T (p.Gly252=)
9g.134887263G>ACA375461574FCN2c.790G>A (p.Ala264Thr)
c.676G>A (p.Ala226Thr)
c.643G>A (p.Ala215Thr)
c.757G>A (p.Ala253Thr)
9g.134887263G>CCA375461572FCN2c.790G>C (p.Ala264Pro)
c.676G>C (p.Ala226Pro)
c.643G>C (p.Ala215Pro)
c.757G>C (p.Ala253Pro)
9g.134887263G=CA1883419552FCN2c.790G= (p.Ala264=)
c.676G= (p.Ala226=)
c.643G= (p.Ala215=)
c.757G= (p.Ala253=)
9g.134887263G>TCA375461573FCN2c.790G>T (p.Ala264Ser)
c.676G>T (p.Ala226Ser)
c.643G>T (p.Ala215Ser)
c.757G>T (p.Ala253Ser)
9g.134887263_134887264delinsGCCA1883419553FCN2c.790_791delinsGC (p.Ala264=)
c.676_677delinsGC (p.Ala226=)
c.643_644delinsGC (p.Ala215=)
c.757_758delinsGC (p.Ala253=)
9g.134887263_134887265delinsGCTCA1883419554FCN2c.790_792delinsGCT (p.Ala264=)
c.676_678delinsGCT (p.Ala226=)
c.643_645delinsGCT (p.Ala215=)
c.757_759delinsGCT (p.Ala253=)
9g.134887264delCA5321365FCN2c.791del (p.Ala264ValfsTer12)
c.677del (p.Ala226ValfsTer12)
c.644del (p.Ala215ValfsTer12)
c.758del (p.Ala253ValfsTer12)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.134887264C>ACA375461575FCN2c.791C>A (p.Ala264Asp)
c.677C>A (p.Ala226Asp)
c.644C>A (p.Ala215Asp)
c.758C>A (p.Ala253Asp)
9g.134887264C>GCA375461576FCN2c.791C>G (p.Ala264Gly)
c.677C>G (p.Ala226Gly)
c.644C>G (p.Ala215Gly)
c.758C>G (p.Ala253Gly)
9g.134887264C>TCA375461577FCN2c.791C>T (p.Ala264Val)
c.677C>T (p.Ala226Val)
c.644C>T (p.Ala215Val)
c.758C>T (p.Ala253Val)
 gnomAD v4
9g.134887264dupCA1883419555FCN2c.791dup (p.Trp265LeufsTer?)
c.677dup (p.Trp227LeufsTer?)
c.644dup (p.Trp216LeufsTer?)
c.758dup (p.Trp254LeufsTer?)
 dbSNP
9g.134887264_134887265delinsACA201116370FCN2c.791_792delinsA (p.Ala264AspfsTer12)
c.677_678delinsA (p.Ala226AspfsTer12)
c.644_645delinsA (p.Ala215AspfsTer12)
c.758_759delinsA (p.Ala253AspfsTer12)
 dbSNP
9g.134887265T>ACA5321366FCN2c.792T>A (p.Ala264=)
c.678T>A (p.Ala226=)
c.645T>A (p.Ala215=)
c.759T>A (p.Ala253=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.134887265T>CCA467816417FCN2c.792T>C (p.Ala264=)
c.678T>C (p.Ala226=)
c.645T>C (p.Ala215=)
c.759T>C (p.Ala253=)
9g.134887265T>GCA467816418FCN2c.792T>G (p.Ala264=)
c.678T>G (p.Ala226=)
c.645T>G (p.Ala215=)
c.759T>G (p.Ala253=)
9g.134887265T=CA1883419556FCN2c.792T= (p.Ala264=)
c.678T= (p.Ala226=)
c.645T= (p.Ala215=)
c.759T= (p.Ala253=)
9g.134887266delCA375461578FCN2c.793del (p.Trp265GlyfsTer11)
c.679del (p.Trp227GlyfsTer11)
c.646del (p.Trp216GlyfsTer11)
c.760del (p.Trp254GlyfsTer11)
9g.134887266T>ACA375461579FCN2c.793T>A (p.Trp265Arg)
c.679T>A (p.Trp227Arg)
c.646T>A (p.Trp216Arg)
c.760T>A (p.Trp254Arg)
9g.134887266T>CCA375461580FCN2c.793T>C (p.Trp265Arg)
c.679T>C (p.Trp227Arg)
c.646T>C (p.Trp216Arg)
c.760T>C (p.Trp254Arg)
9g.134887266T>GCA375461581FCN2c.793T>G (p.Trp265Gly)
c.679T>G (p.Trp227Gly)
c.646T>G (p.Trp216Gly)
c.760T>G (p.Trp254Gly)
9g.134887267G>ACA375461582FCN2c.794G>A (p.Trp265Ter)
c.680G>A (p.Trp227Ter)
c.647G>A (p.Trp216Ter)
c.761G>A (p.Trp254Ter)
9g.134887267G>CCA375461583FCN2c.794G>C (p.Trp265Ser)
c.680G>C (p.Trp227Ser)
c.647G>C (p.Trp216Ser)
c.761G>C (p.Trp254Ser)
9g.134887267G>TCA375461584FCN2c.794G>T (p.Trp265Leu)
c.680G>T (p.Trp227Leu)
c.647G>T (p.Trp216Leu)
c.761G>T (p.Trp254Leu)
9g.134887268G>ACA375461585FCN2c.795G>A (p.Trp265Ter)
c.681G>A (p.Trp227Ter)
c.648G>A (p.Trp216Ter)
c.762G>A (p.Trp254Ter)
9g.134887268G>CCA375461587FCN2c.795G>C (p.Trp265Cys)
c.681G>C (p.Trp227Cys)
c.648G>C (p.Trp216Cys)
c.762G>C (p.Trp254Cys)
9g.134887268G>TCA375461586FCN2c.795G>T (p.Trp265Cys)
c.681G>T (p.Trp227Cys)
c.648G>T (p.Trp216Cys)
c.762G>T (p.Trp254Cys)
9g.134887269T>ACA375461588FCN2c.796T>A (p.Trp266Arg)
c.682T>A (p.Trp228Arg)
c.649T>A (p.Trp217Arg)
c.763T>A (p.Trp255Arg)
 COSMIC
9g.134887269T>CCA375461589FCN2c.796T>C (p.Trp266Arg)
c.682T>C (p.Trp228Arg)
c.649T>C (p.Trp217Arg)
c.763T>C (p.Trp255Arg)
 gnomAD v4
9g.134887269T>GCA375461590FCN2c.796T>G (p.Trp266Gly)
c.682T>G (p.Trp228Gly)
c.649T>G (p.Trp217Gly)
c.763T>G (p.Trp255Gly)
9g.134887270G>ACA5321367FCN2c.797G>A (p.Trp266Ter)
c.683G>A (p.Trp228Ter)
c.650G>A (p.Trp217Ter)
c.764G>A (p.Trp255Ter)
 dbSNP ExAC gnomAD v2 gnomAD v4
9g.134887270G>CCA375461591FCN2c.797G>C (p.Trp266Ser)
c.683G>C (p.Trp228Ser)
c.650G>C (p.Trp217Ser)
c.764G>C (p.Trp255Ser)
 dbSNP
9g.134887270G=CA1883419557FCN2c.797G= (p.Trp266=)
c.683G= (p.Trp228=)
c.650G= (p.Trp217=)
c.764G= (p.Trp255=)
9g.134887270G>TCA5321368FCN2c.797G>T (p.Trp266Leu)
c.683G>T (p.Trp228Leu)
c.650G>T (p.Trp217Leu)
c.764G>T (p.Trp255Leu)
 dbSNP ExAC gnomAD v2 gnomAD v4
9g.134887271G>ACA375461592FCN2c.798G>A (p.Trp266Ter)
c.684G>A (p.Trp228Ter)
c.651G>A (p.Trp217Ter)
c.765G>A (p.Trp255Ter)
9g.134887271G>CCA375461593FCN2c.798G>C (p.Trp266Cys)
c.684G>C (p.Trp228Cys)
c.651G>C (p.Trp217Cys)
c.765G>C (p.Trp255Cys)
9g.134887271G>TCA375461594FCN2c.798G>T (p.Trp266Cys)
c.684G>T (p.Trp228Cys)
c.651G>T (p.Trp217Cys)
c.765G>T (p.Trp255Cys)
9g.134887272T>ACA375461595FCN2c.799T>A (p.Tyr267Asn)
c.685T>A (p.Tyr229Asn)
c.652T>A (p.Tyr218Asn)
c.766T>A (p.Tyr256Asn)
9g.134887272T>CCA375461596FCN2c.799T>C (p.Tyr267His)
c.685T>C (p.Tyr229His)
c.652T>C (p.Tyr218His)
c.766T>C (p.Tyr256His)
 gnomAD v4
9g.134887272T>GCA375461597FCN2c.799T>G (p.Tyr267Asp)
c.685T>G (p.Tyr229Asp)
c.652T>G (p.Tyr218Asp)
c.766T>G (p.Tyr256Asp)
9g.134887273A>CCA375461600FCN2c.800A>C (p.Tyr267Ser)
c.686A>C (p.Tyr229Ser)
c.653A>C (p.Tyr218Ser)
c.767A>C (p.Tyr256Ser)
 gnomAD v4
9g.134887273A>GCA375461598FCN2c.800A>G (p.Tyr267Cys)
c.686A>G (p.Tyr229Cys)
c.653A>G (p.Tyr218Cys)
c.767A>G (p.Tyr256Cys)
 gnomAD v4
9g.134887273A>TCA375461599FCN2c.800A>T (p.Tyr267Phe)
c.686A>T (p.Tyr229Phe)
c.653A>T (p.Tyr218Phe)
c.767A>T (p.Tyr256Phe)
9g.134887274C>ACA375461601FCN2c.801C>A (p.Tyr267Ter)
c.687C>A (p.Tyr229Ter)
c.654C>A (p.Tyr218Ter)
c.768C>A (p.Tyr256Ter)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.134887274C=CA1883419558FCN2c.801C= (p.Tyr267=)
c.687C= (p.Tyr229=)
c.654C= (p.Tyr218=)
c.768C= (p.Tyr256=)
9g.134887274C>GCA375461602FCN2c.801C>G (p.Tyr267Ter)
c.687C>G (p.Tyr229Ter)
c.654C>G (p.Tyr218Ter)
c.768C>G (p.Tyr256Ter)
9g.134887274C>TCA467816419FCN2c.801C>T (p.Tyr267=)
c.687C>T (p.Tyr229=)
c.654C>T (p.Tyr218=)
c.768C>T (p.Tyr256=)
 gnomAD v4
9g.134887275A>CCA375461603FCN2c.802A>C (p.Lys268Gln)
c.688A>C (p.Lys230Gln)
c.655A>C (p.Lys219Gln)
c.769A>C (p.Lys257Gln)
9g.134887275A>GCA375461604FCN2c.802A>G (p.Lys268Glu)
c.688A>G (p.Lys230Glu)
c.655A>G (p.Lys219Glu)
c.769A>G (p.Lys257Glu)
9g.134887275A>TCA375461605FCN2c.802A>T (p.Lys268Ter)
c.688A>T (p.Lys230Ter)
c.655A>T (p.Lys219Ter)
c.769A>T (p.Lys257Ter)
9g.134887278_134887279delCA2579507595FCN2c.805_806del (p.Asn269LeufsTer?)
c.691_692del (p.Asn231LeufsTer?)
c.658_659del (p.Asn220LeufsTer?)
c.772_773del (p.Asn258LeufsTer?)
9g.134887276A=CA1883419559FCN2c.803A= (p.Lys268=)
c.689A= (p.Lys230=)
c.656A= (p.Lys219=)
c.770A= (p.Lys257=)
9g.134887276A>CCA5321369FCN2c.803A>C (p.Lys268Thr)
c.689A>C (p.Lys230Thr)
c.656A>C (p.Lys219Thr)
c.770A>C (p.Lys257Thr)
 dbSNP ExAC gnomAD v3 gnomAD v4
9g.134887276A>GCA375461606FCN2c.803A>G (p.Lys268Arg)
c.689A>G (p.Lys230Arg)
c.656A>G (p.Lys219Arg)
c.770A>G (p.Lys257Arg)
 COSMIC
9g.134887276A>TCA375461607FCN2c.803A>T (p.Lys268Ile)
c.689A>T (p.Lys230Ile)
c.656A>T (p.Lys219Ile)
c.770A>T (p.Lys257Ile)
9g.134887277A>CCA375461608FCN2c.804A>C (p.Lys268Asn)
c.690A>C (p.Lys230Asn)
c.657A>C (p.Lys219Asn)
c.771A>C (p.Lys257Asn)
9g.134887277A>GCA467816421FCN2c.804A>G (p.Lys268=)
c.690A>G (p.Lys230=)
c.657A>G (p.Lys219=)
c.771A>G (p.Lys257=)
9g.134887277A>TCA375461609FCN2c.804A>T (p.Lys268Asn)
c.690A>T (p.Lys230Asn)
c.657A>T (p.Lys219Asn)
c.771A>T (p.Lys257Asn)
9g.134887278A>CCA375461612FCN2c.805A>C (p.Asn269His)
c.691A>C (p.Asn231His)
c.658A>C (p.Asn220His)
c.772A>C (p.Asn258His)
9g.134887278A>GCA375461611FCN2c.805A>G (p.Asn269Asp)
c.691A>G (p.Asn231Asp)
c.658A>G (p.Asn220Asp)
c.772A>G (p.Asn258Asp)
9g.134887278A>TCA375461610FCN2c.805A>T (p.Asn269Tyr)
c.691A>T (p.Asn231Tyr)
c.658A>T (p.Asn220Tyr)
c.772A>T (p.Asn258Tyr)
9g.134887279A>CCA375461613FCN2c.806A>C (p.Asn269Thr)
c.692A>C (p.Asn231Thr)
c.659A>C (p.Asn220Thr)
c.773A>C (p.Asn258Thr)
9g.134887279A>GCA375461615FCN2c.806A>G (p.Asn269Ser)
c.692A>G (p.Asn231Ser)
c.659A>G (p.Asn220Ser)
c.773A>G (p.Asn258Ser)
9g.134887279A>TCA375461614FCN2c.806A>T (p.Asn269Ile)
c.692A>T (p.Asn231Ile)
c.659A>T (p.Asn220Ile)
c.773A>T (p.Asn258Ile)
9g.134887280C>ACA375461616FCN2c.807C>A (p.Asn269Lys)
c.693C>A (p.Asn231Lys)
c.660C>A (p.Asn220Lys)
c.774C>A (p.Asn258Lys)
9g.134887280C=CA1883419560FCN2c.807C= (p.Asn269=)
c.693C= (p.Asn231=)
c.660C= (p.Asn220=)
c.774C= (p.Asn258=)
9g.134887280C>GCA375461617FCN2c.807C>G (p.Asn269Lys)
c.693C>G (p.Asn231Lys)
c.660C>G (p.Asn220Lys)
c.774C>G (p.Asn258Lys)
9g.134887280C>TCA5321370FCN2c.807C>T (p.Asn269=)
c.693C>T (p.Asn231=)
c.660C>T (p.Asn220=)
c.774C>T (p.Asn258=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.134887281T>ACA375461618FCN2c.808T>A (p.Cys270Ser)
c.694T>A (p.Cys232Ser)
c.661T>A (p.Cys221Ser)
c.775T>A (p.Cys259Ser)
9g.134887281T>CCA375461619FCN2c.808T>C (p.Cys270Arg)
c.694T>C (p.Cys232Arg)
c.661T>C (p.Cys221Arg)
c.775T>C (p.Cys259Arg)
9g.134887281T>GCA375461620FCN2c.808T>G (p.Cys270Gly)
c.694T>G (p.Cys232Gly)
c.661T>G (p.Cys221Gly)
c.775T>G (p.Cys259Gly)
9g.134887282G>ACA375461621FCN2c.809G>A (p.Cys270Tyr)
c.695G>A (p.Cys232Tyr)
c.662G>A (p.Cys221Tyr)
c.776G>A (p.Cys259Tyr)
 dbSNP gnomAD v2 gnomAD v4
9g.134887282G>CCA375461622FCN2c.809G>C (p.Cys270Ser)
c.695G>C (p.Cys232Ser)
c.662G>C (p.Cys221Ser)
c.776G>C (p.Cys259Ser)
9g.134887282G=CA1883419561FCN2c.809G= (p.Cys270=)
c.695G= (p.Cys232=)
c.662G= (p.Cys221=)
c.776G= (p.Cys259=)
9g.134887282G>TCA375461623FCN2c.809G>T (p.Cys270Phe)
c.695G>T (p.Cys232Phe)
c.662G>T (p.Cys221Phe)
c.776G>T (p.Cys259Phe)
 gnomAD v4
9g.134887283C>ACA375461624FCN2c.810C>A (p.Cys270Ter)
c.696C>A (p.Cys232Ter)
c.663C>A (p.Cys221Ter)
c.777C>A (p.Cys259Ter)
9g.134887283C>GCA375461625FCN2c.810C>G (p.Cys270Trp)
c.696C>G (p.Cys232Trp)
c.663C>G (p.Cys221Trp)
c.777C>G (p.Cys259Trp)
9g.134887283C>TCA467816422FCN2c.810C>T (p.Cys270=)
c.696C>T (p.Cys232=)
c.663C>T (p.Cys221=)
c.777C>T (p.Cys259=)
 gnomAD v4
9g.134887284C>ACA375461628FCN2c.811C>A (p.His271Asn)
c.697C>A (p.His233Asn)
c.664C>A (p.His222Asn)
c.778C>A (p.His260Asn)
9g.134887284C>GCA375461627FCN2c.811C>G (p.His271Asp)
c.697C>G (p.His233Asp)
c.664C>G (p.His222Asp)
c.778C>G (p.His260Asp)
9g.134887284C>TCA375461626FCN2c.811C>T (p.His271Tyr)
c.697C>T (p.His233Tyr)
c.664C>T (p.His222Tyr)
c.778C>T (p.His260Tyr)
9g.134887285A>CCA375461629FCN2c.812A>C (p.His271Pro)
c.698A>C (p.His233Pro)
c.665A>C (p.His222Pro)
c.779A>C (p.His260Pro)
9g.134887285A>GCA375461630FCN2c.812A>G (p.His271Arg)
c.698A>G (p.His233Arg)
c.665A>G (p.His222Arg)
c.779A>G (p.His260Arg)
9g.134887285A>TCA375461631FCN2c.812A>T (p.His271Leu)
c.698A>T (p.His233Leu)
c.665A>T (p.His222Leu)
c.779A>T (p.His260Leu)
9g.134887286T>ACA375461632FCN2c.813T>A (p.His271Gln)
c.699T>A (p.His233Gln)
c.666T>A (p.His222Gln)
c.780T>A (p.His260Gln)
 dbSNP gnomAD v3 gnomAD v4
9g.134887286T>CCA467816423FCN2c.813T>C (p.His271=)
c.699T>C (p.His233=)
c.666T>C (p.His222=)
c.780T>C (p.His260=)
 dbSNP gnomAD v4
9g.134887286T>GCA375461633FCN2c.813T>G (p.His271Gln)
c.699T>G (p.His233Gln)
c.666T>G (p.His222Gln)
c.780T>G (p.His260Gln)
9g.134887286T=CA1883419562FCN2c.813T= (p.His271=)
c.699T= (p.His233=)
c.666T= (p.His222=)
c.780T= (p.His260=)
9g.134887287G>ACA375461634FCN2c.814G>A (p.Val272Met)
c.700G>A (p.Val234Met)
c.667G>A (p.Val223Met)
c.781G>A (p.Val261Met)
 dbSNP gnomAD v3 gnomAD v4 COSMIC
9g.134887287G>CCA375461635FCN2c.814G>C (p.Val272Leu)
c.700G>C (p.Val234Leu)
c.667G>C (p.Val223Leu)
c.781G>C (p.Val261Leu)
9g.134887287G>TCA375461636FCN2c.814G>T (p.Val272Leu)
c.700G>T (p.Val234Leu)
c.667G>T (p.Val223Leu)
c.781G>T (p.Val261Leu)
9g.134887288T>ACA375461637FCN2c.815T>A (p.Val272Glu)
c.701T>A (p.Val234Glu)
c.668T>A (p.Val223Glu)
c.782T>A (p.Val261Glu)
9g.134887288T>CCA375461638FCN2c.815T>C (p.Val272Ala)
c.701T>C (p.Val234Ala)
c.668T>C (p.Val223Ala)
c.782T>C (p.Val261Ala)
9g.134887288T>GCA375461639FCN2c.815T>G (p.Val272Gly)
c.701T>G (p.Val234Gly)
c.668T>G (p.Val223Gly)
c.782T>G (p.Val261Gly)
9g.134887289G>ACA467816424FCN2c.816G>A (p.Val272=)
c.702G>A (p.Val234=)
c.669G>A (p.Val223=)
c.783G>A (p.Val261=)
9g.134887289G>CCA467816426FCN2c.816G>C (p.Val272=)
c.702G>C (p.Val234=)
c.669G>C (p.Val223=)
c.783G>C (p.Val261=)
9g.134887289G>TCA467816425FCN2c.816G>T (p.Val272=)
c.702G>T (p.Val234=)
c.669G>T (p.Val223=)
c.783G>T (p.Val261=)
9g.134887290T>ACA375461642FCN2c.817T>A (p.Ser273Thr)
c.703T>A (p.Ser235Thr)
c.670T>A (p.Ser224Thr)
c.784T>A (p.Ser262Thr)
9g.134887290T>CCA375461641FCN2c.817T>C (p.Ser273Pro)
c.703T>C (p.Ser235Pro)
c.670T>C (p.Ser224Pro)
c.784T>C (p.Ser262Pro)
9g.134887290T>GCA375461640FCN2c.817T>G (p.Ser273Ala)
c.703T>G (p.Ser235Ala)
c.670T>G (p.Ser224Ala)
c.784T>G (p.Ser262Ala)
9g.134887291C>ACA375461643FCN2c.818C>A (p.Ser273Ter)
c.704C>A (p.Ser235Ter)
c.671C>A (p.Ser224Ter)
c.785C>A (p.Ser262Ter)
9g.134887291C=CA1883419563FCN2c.818C= (p.Ser273=)
c.704C= (p.Ser235=)
c.671C= (p.Ser224=)
c.785C= (p.Ser262=)
9g.134887291C>GCA5321371FCN2c.818C>G (p.Ser273Ter)
c.704C>G (p.Ser235Ter)
c.671C>G (p.Ser224Ter)
c.785C>G (p.Ser262Ter)
 dbSNP ExAC gnomAD v2 gnomAD v4
9g.134887291C>TCA375461644FCN2c.818C>T (p.Ser273Leu)
c.704C>T (p.Ser235Leu)
c.671C>T (p.Ser224Leu)
c.785C>T (p.Ser262Leu)
 COSMIC
9g.134887292A=CA1883419564FCN2c.819A= (p.Ser273=)
c.705A= (p.Ser235=)
c.672A= (p.Ser224=)
c.786A= (p.Ser262=)
9g.134887292A>CCA5321372FCN2c.819A>C (p.Ser273=)
c.705A>C (p.Ser235=)
c.672A>C (p.Ser224=)
c.786A>C (p.Ser262=)
 dbSNP ExAC gnomAD v2 gnomAD v4
9g.134887292A>GCA467816428FCN2c.819A>G (p.Ser273=)
c.705A>G (p.Ser235=)
c.672A>G (p.Ser224=)
c.786A>G (p.Ser262=)
9g.134887292A>TCA467816427FCN2c.819A>T (p.Ser273=)
c.705A>T (p.Ser235=)
c.672A>T (p.Ser224=)
c.786A>T (p.Ser262=)
9g.134887293A>CCA375461645FCN2c.820A>C (p.Asn274His)
c.706A>C (p.Asn236His)
c.673A>C (p.Asn225His)
c.787A>C (p.Asn263His)
9g.134887293A>GCA375461646FCN2c.820A>G (p.Asn274Asp)
c.706A>G (p.Asn236Asp)
c.673A>G (p.Asn225Asp)
c.787A>G (p.Asn263Asp)
9g.134887293A>TCA375461647FCN2c.820A>T (p.Asn274Tyr)
c.706A>T (p.Asn236Tyr)
c.673A>T (p.Asn225Tyr)
c.787A>T (p.Asn263Tyr)
9g.134887294A=CA1883419565FCN2c.821A= (p.Asn274=)
c.707A= (p.Asn236=)
c.674A= (p.Asn225=)
c.788A= (p.Asn263=)
9g.134887294A>CCA375461648FCN2c.821A>C (p.Asn274Thr)
c.707A>C (p.Asn236Thr)
c.674A>C (p.Asn225Thr)
c.788A>C (p.Asn263Thr)
9g.134887294A>GCA375461650FCN2c.821A>G (p.Asn274Ser)
c.707A>G (p.Asn236Ser)
c.674A>G (p.Asn225Ser)
c.788A>G (p.Asn263Ser)
 dbSNP gnomAD v2 gnomAD v4
9g.134887294A>TCA375461649FCN2c.821A>T (p.Asn274Ile)
c.707A>T (p.Asn236Ile)
c.674A>T (p.Asn225Ile)
c.788A>T (p.Asn263Ile)
9g.134887295C>ACA375461651FCN2c.822C>A (p.Asn274Lys)
c.708C>A (p.Asn236Lys)
c.675C>A (p.Asn225Lys)
c.789C>A (p.Asn263Lys)
 gnomAD v4
9g.134887295C>GCA375461652FCN2c.822C>G (p.Asn274Lys)
c.708C>G (p.Asn236Lys)
c.675C>G (p.Asn225Lys)
c.789C>G (p.Asn263Lys)
9g.134887295C>TCA467816429FCN2c.822C>T (p.Asn274=)
c.708C>T (p.Asn236=)
c.675C>T (p.Asn225=)
c.789C>T (p.Asn263=)
 gnomAD v4
9g.134887295_134887296dupCA2741061244FCN2c.822_823dup (p.Leu275ProfsTer2)
c.708_709dup (p.Leu237ProfsTer2)
c.675_676dup (p.Leu226ProfsTer2)
c.789_790dup (p.Leu264ProfsTer2)
9g.134887296C>ACA375461653FCN2c.823C>A (p.Leu275Met)
c.709C>A (p.Leu237Met)
c.676C>A (p.Leu226Met)
c.790C>A (p.Leu264Met)
9g.134887296C=CA1883419566FCN2c.823C= (p.Leu275=)
c.709C= (p.Leu237=)
c.676C= (p.Leu226=)
c.790C= (p.Leu264=)
9g.134887296C>GCA5321373FCN2c.823C>G (p.Leu275Val)
c.709C>G (p.Leu237Val)
c.676C>G (p.Leu226Val)
c.790C>G (p.Leu264Val)
 dbSNP ExAC gnomAD v2 gnomAD v4
9g.134887296C>TCA467816430FCN2c.823C>T (p.Leu275=)
c.709C>T (p.Leu237=)
c.676C>T (p.Leu226=)
c.790C>T (p.Leu264=)
9g.134887297T>ACA375461654FCN2c.824T>A (p.Leu275Gln)
c.710T>A (p.Leu237Gln)
c.677T>A (p.Leu226Gln)
c.791T>A (p.Leu264Gln)
9g.134887297T>CCA375461656FCN2c.824T>C (p.Leu275Pro)
c.710T>C (p.Leu237Pro)
c.677T>C (p.Leu226Pro)
c.791T>C (p.Leu264Pro)
9g.134887297T>GCA375461655FCN2c.824T>G (p.Leu275Arg)
c.710T>G (p.Leu237Arg)
c.677T>G (p.Leu226Arg)
c.791T>G (p.Leu264Arg)
9g.134887298G>ACA467816431FCN2c.825G>A (p.Leu275=)
c.711G>A (p.Leu237=)
c.678G>A (p.Leu226=)
c.792G>A (p.Leu264=)
9g.134887298G>CCA467816432FCN2c.825G>C (p.Leu275=)
c.711G>C (p.Leu237=)
c.678G>C (p.Leu226=)
c.792G>C (p.Leu264=)
9g.134887298G>TCA467816433FCN2c.825G>T (p.Leu275=)
c.711G>T (p.Leu237=)
c.678G>T (p.Leu226=)
c.792G>T (p.Leu264=)
 dbSNP gnomAD v4
9g.134887299A>CCA375461657FCN2c.826A>C (p.Asn276His)
c.712A>C (p.Asn238His)
c.679A>C (p.Asn227His)
c.793A>C (p.Asn265His)
9g.134887299A>GCA375461658FCN2c.826A>G (p.Asn276Asp)
c.712A>G (p.Asn238Asp)
c.679A>G (p.Asn227Asp)
c.793A>G (p.Asn265Asp)
 dbSNP
9g.134887299A>TCA375461659FCN2c.826A>T (p.Asn276Tyr)
c.712A>T (p.Asn238Tyr)
c.679A>T (p.Asn227Tyr)
c.793A>T (p.Asn265Tyr)
9g.134887300A=CA1883419567FCN2c.827A= (p.Asn276=)
c.713A= (p.Asn238=)
c.680A= (p.Asn227=)
c.794A= (p.Asn265=)
9g.134887300A>CCA375461660FCN2c.827A>C (p.Asn276Thr)
c.713A>C (p.Asn238Thr)
c.680A>C (p.Asn227Thr)
c.794A>C (p.Asn265Thr)
9g.134887300A>GCA5321374FCN2c.827A>G (p.Asn276Ser)
c.713A>G (p.Asn238Ser)
c.680A>G (p.Asn227Ser)
c.794A>G (p.Asn265Ser)
 dbSNP ExAC gnomAD v2 gnomAD v4
9g.134887300A>TCA375461661FCN2c.827A>T (p.Asn276Ile)
c.713A>T (p.Asn238Ile)
c.680A>T (p.Asn227Ile)
c.794A>T (p.Asn265Ile)
9g.134887300_134887301delCA2741061245FCN2c.827_828del (p.Asn276ArgfsTer26)
c.713_714del (p.Asn238ArgfsTer26)
c.680_681del (p.Asn227ArgfsTer26)
c.794_795del (p.Asn265ArgfsTer26)
9g.134887301T>ACA375461662FCN2c.828T>A (p.Asn276Lys)
c.714T>A (p.Asn238Lys)
c.681T>A (p.Asn227Lys)
c.795T>A (p.Asn265Lys)
9g.134887301T>CCA467816434FCN2c.828T>C (p.Asn276=)
c.714T>C (p.Asn238=)
c.681T>C (p.Asn227=)
c.795T>C (p.Asn265=)
9g.134887301T>GCA375461663FCN2c.828T>G (p.Asn276Lys)
c.714T>G (p.Asn238Lys)
c.681T>G (p.Asn227Lys)
c.795T>G (p.Asn265Lys)
9g.134887302G>ACA375461664FCN2c.829G>A (p.Gly277Ser)
c.715G>A (p.Gly239Ser)
c.682G>A (p.Gly228Ser)
c.796G>A (p.Gly266Ser)
9g.134887302G>CCA375461665FCN2c.829G>C (p.Gly277Arg)
c.715G>C (p.Gly239Arg)
c.682G>C (p.Gly228Arg)
c.796G>C (p.Gly266Arg)
 gnomAD v4
9g.134887302G>TCA375461666FCN2c.829G>T (p.Gly277Cys)
c.715G>T (p.Gly239Cys)
c.682G>T (p.Gly228Cys)
c.796G>T (p.Gly266Cys)
 gnomAD v4
9g.134887303G>ACA5321375FCN2c.830G>A (p.Gly277Asp)
c.716G>A (p.Gly239Asp)
c.683G>A (p.Gly228Asp)
c.797G>A (p.Gly266Asp)
 dbSNP ExAC gnomAD v2 gnomAD v4
9g.134887303G>CCA375461668FCN2c.830G>C (p.Gly277Ala)
c.716G>C (p.Gly239Ala)
c.683G>C (p.Gly228Ala)
c.797G>C (p.Gly266Ala)
 gnomAD v4
9g.134887303G=CA1883419568FCN2c.830G= (p.Gly277=)
c.716G= (p.Gly239=)
c.683G= (p.Gly228=)
c.797G= (p.Gly266=)
9g.134887303G>TCA375461667FCN2c.830G>T (p.Gly277Val)
c.716G>T (p.Gly239Val)
c.683G>T (p.Gly228Val)
c.797G>T (p.Gly266Val)
 dbSNP gnomAD v2 gnomAD v4 COSMIC
9g.134887304T>ACA467816435FCN2c.831T>A (p.Gly277=)
c.717T>A (p.Gly239=)
c.684T>A (p.Gly228=)
c.798T>A (p.Gly266=)
9g.134887304T>CCA467816436FCN2c.831T>C (p.Gly277=)
c.717T>C (p.Gly239=)
c.684T>C (p.Gly228=)
c.798T>C (p.Gly266=)
9g.134887304T>GCA467816437FCN2c.831T>G (p.Gly277=)
c.717T>G (p.Gly239=)
c.684T>G (p.Gly228=)
c.798T>G (p.Gly266=)
9g.134887305C>ACA375461670FCN2c.832C>A (p.Arg278Ser)
c.718C>A (p.Arg240Ser)
c.685C>A (p.Arg229Ser)
c.799C>A (p.Arg267Ser)
9g.134887305C=CA1883419569FCN2c.832C= (p.Arg278=)
c.718C= (p.Arg240=)
c.685C= (p.Arg229=)
c.799C= (p.Arg267=)
9g.134887305C>GCA375461669FCN2c.832C>G (p.Arg278Gly)
c.718C>G (p.Arg240Gly)
c.685C>G (p.Arg229Gly)
c.799C>G (p.Arg267Gly)
9g.134887305C>TCA5321376FCN2c.832C>T (p.Arg278Cys)
c.718C>T (p.Arg240Cys)
c.685C>T (p.Arg229Cys)
c.799C>T (p.Arg267Cys)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
9g.134887306G>ACA5321377FCN2c.833G>A (p.Arg278His)
c.719G>A (p.Arg240His)
c.686G>A (p.Arg229His)
c.800G>A (p.Arg267His)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.134887306G>CCA375461671FCN2c.833G>C (p.Arg278Pro)
c.719G>C (p.Arg240Pro)
c.686G>C (p.Arg229Pro)
c.800G>C (p.Arg267Pro)
9g.134887306G=CA1883419570FCN2c.833G= (p.Arg278=)
c.719G= (p.Arg240=)
c.686G= (p.Arg229=)
c.800G= (p.Arg267=)
9g.134887306G>TCA201116435FCN2c.833G>T (p.Arg278Leu)
c.719G>T (p.Arg240Leu)
c.686G>T (p.Arg229Leu)
c.800G>T (p.Arg267Leu)
 dbSNP gnomAD v4
9g.134887307C>ACA5321378FCN2c.834C>A (p.Arg278=)
c.720C>A (p.Arg240=)
c.687C>A (p.Arg229=)
c.801C>A (p.Arg267=)
 dbSNP ExAC gnomAD v2 gnomAD v4
9g.134887307C=CA1883419571FCN2c.834C= (p.Arg278=)
c.720C= (p.Arg240=)
c.687C= (p.Arg229=)
c.801C= (p.Arg267=)
9g.134887307C>GCA467816438FCN2c.834C>G (p.Arg278=)
c.720C>G (p.Arg240=)
c.687C>G (p.Arg229=)
c.801C>G (p.Arg267=)
9g.134887307C>TCA467816439FCN2c.834C>T (p.Arg278=)
c.720C>T (p.Arg240=)
c.687C>T (p.Arg229=)
c.801C>T (p.Arg267=)
 gnomAD v4
9g.134887308T>ACA375461672FCN2c.835T>A (p.Tyr279Asn)
c.721T>A (p.Tyr241Asn)
c.688T>A (p.Tyr230Asn)
c.802T>A (p.Tyr268Asn)
 dbSNP gnomAD v3 gnomAD v4
9g.134887308T>CCA375461673FCN2c.835T>C (p.Tyr279His)
c.721T>C (p.Tyr241His)
c.688T>C (p.Tyr230His)
c.802T>C (p.Tyr268His)
 gnomAD v4
9g.134887308T>GCA375461675FCN2c.835T>G (p.Tyr279Asp)
c.721T>G (p.Tyr241Asp)
c.688T>G (p.Tyr230Asp)
c.802T>G (p.Tyr268Asp)
9g.134887308T=CA1883419572FCN2c.835T= (p.Tyr279=)
c.721T= (p.Tyr241=)
c.688T= (p.Tyr230=)
c.802T= (p.Tyr268=)
9g.134887309A=CA1883419573FCN2c.836A= (p.Tyr279=)
c.722A= (p.Tyr241=)
c.689A= (p.Tyr230=)
c.803A= (p.Tyr268=)
9g.134887309A>CCA375461677FCN2c.836A>C (p.Tyr279Ser)
c.722A>C (p.Tyr241Ser)
c.689A>C (p.Tyr230Ser)
c.803A>C (p.Tyr268Ser)
9g.134887309A>GCA5321379FCN2c.836A>G (p.Tyr279Cys)
c.722A>G (p.Tyr241Cys)
c.689A>G (p.Tyr230Cys)
c.803A>G (p.Tyr268Cys)
 dbSNP ExAC gnomAD v2 gnomAD v4
9g.134887309A>TCA375461680FCN2c.836A>T (p.Tyr279Phe)
c.722A>T (p.Tyr241Phe)
c.689A>T (p.Tyr230Phe)
c.803A>T (p.Tyr268Phe)
9g.134887310C>ACA375461683FCN2c.837C>A (p.Tyr279Ter)
c.723C>A (p.Tyr241Ter)
c.690C>A (p.Tyr230Ter)
c.804C>A (p.Tyr268Ter)
9g.134887310C=CA1883419574FCN2c.837C= (p.Tyr279=)
c.723C= (p.Tyr241=)
c.690C= (p.Tyr230=)
c.804C= (p.Tyr268=)
9g.134887310C>GCA375461685FCN2c.837C>G (p.Tyr279Ter)
c.723C>G (p.Tyr241Ter)
c.690C>G (p.Tyr230Ter)
c.804C>G (p.Tyr268Ter)
 dbSNP gnomAD v3 gnomAD v4
9g.134887310C>TCA467816440FCN2c.837C>T (p.Tyr279=)
c.723C>T (p.Tyr241=)
c.690C>T (p.Tyr230=)
c.804C>T (p.Tyr268=)
9g.134887311C>ACA375461688FCN2c.838C>A (p.Leu280Ile)
c.724C>A (p.Leu242Ile)
c.691C>A (p.Leu231Ile)
c.805C>A (p.Leu269Ile)
9g.134887311C>GCA375461689FCN2c.838C>G (p.Leu280Val)
c.724C>G (p.Leu242Val)
c.691C>G (p.Leu231Val)
c.805C>G (p.Leu269Val)
9g.134887311C>TCA375461691FCN2c.838C>T (p.Leu280Phe)
c.724C>T (p.Leu242Phe)
c.691C>T (p.Leu231Phe)
c.805C>T (p.Leu269Phe)
 gnomAD v4
9g.134887311_134887312insATCA2741061246FCN2c.838_839insAT (p.Leu280HisfsTer30)
c.724_725insAT (p.Leu242HisfsTer30)
c.691_692insAT (p.Leu231HisfsTer30)
c.805_806insAT (p.Leu269HisfsTer30)
9g.134887312T>ACA375461697FCN2c.839T>A (p.Leu280His)
c.725T>A (p.Leu242His)
c.692T>A (p.Leu231His)
c.806T>A (p.Leu269His)
9g.134887312T>CCA375461694FCN2c.839T>C (p.Leu280Pro)
c.725T>C (p.Leu242Pro)
c.692T>C (p.Leu231Pro)
c.806T>C (p.Leu269Pro)
9g.134887312T>GCA375461695FCN2c.839T>G (p.Leu280Arg)
c.725T>G (p.Leu242Arg)
c.692T>G (p.Leu231Arg)
c.806T>G (p.Leu269Arg)
9g.134887313C>ACA467816441FCN2c.840C>A (p.Leu280=)
c.726C>A (p.Leu242=)
c.693C>A (p.Leu231=)
c.807C>A (p.Leu269=)
9g.134887313C=CA1883419575FCN2c.840C= (p.Leu280=)
c.726C= (p.Leu242=)
c.693C= (p.Leu231=)
c.807C= (p.Leu269=)
9g.134887313C>GCA467816442FCN2c.840C>G (p.Leu280=)
c.726C>G (p.Leu242=)
c.693C>G (p.Leu231=)
c.807C>G (p.Leu269=)
 gnomAD v4
9g.134887313C>TCA5321381FCN2c.840C>T (p.Leu280=)
c.726C>T (p.Leu242=)
c.693C>T (p.Leu231=)
c.807C>T (p.Leu269=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.134887313_134887314delinsCACA1883419576FCN2c.840_841delinsCA (p.Leu280=)
c.726_727delinsCA (p.Leu242=)
c.693_694delinsCA (p.Leu231=)
c.807_808delinsCA (p.Leu269=)
9g.134887314delCA5321380FCN2c.841del (p.Arg281GlyfsTer28)
c.727del (p.Arg243GlyfsTer28)
c.694del (p.Arg232GlyfsTer28)
c.808del (p.Arg270GlyfsTer28)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.134887314A>CCA467816443FCN2c.841A>C (p.Arg281=)
c.727A>C (p.Arg243=)
c.694A>C (p.Arg232=)
c.808A>C (p.Arg270=)
9g.134887314A>GCA375461701FCN2c.841A>G (p.Arg281Gly)
c.727A>G (p.Arg243Gly)
c.694A>G (p.Arg232Gly)
c.808A>G (p.Arg270Gly)
9g.134887314A>TCA375461703FCN2c.841A>T (p.Arg281Trp)
c.727A>T (p.Arg243Trp)
c.694A>T (p.Arg232Trp)
c.808A>T (p.Arg270Trp)
9g.134887315G>ACA375461707FCN2c.842G>A (p.Arg281Lys)
c.728G>A (p.Arg243Lys)
c.695G>A (p.Arg232Lys)
c.809G>A (p.Arg270Lys)
9g.134887315G>CCA375461708FCN2c.842G>C (p.Arg281Thr)
c.728G>C (p.Arg243Thr)
c.695G>C (p.Arg232Thr)
c.809G>C (p.Arg270Thr)
 gnomAD v4
9g.134887315G>TCA375461710FCN2c.842G>T (p.Arg281Met)
c.728G>T (p.Arg243Met)
c.695G>T (p.Arg232Met)
c.809G>T (p.Arg270Met)
9g.134887319dupCA2786220135FCN2c.846dup (p.Thr283AspfsTer20)
c.732dup (p.Thr245AspfsTer20)
c.699dup (p.Thr234AspfsTer20)
c.813dup (p.Thr272AspfsTer20)
9g.134887319delCA2692465630FCN2c.846del (p.Thr283LeufsTer26)
c.732del (p.Thr245LeufsTer26)
c.699del (p.Thr234LeufsTer26)
c.813del (p.Thr272LeufsTer26)
 gnomAD v4
9g.134887318_134887319delCA2741061247FCN2c.845_846del (p.Gly282AspfsTer20)
c.731_732del (p.Gly244AspfsTer20)
c.698_699del (p.Gly233AspfsTer20)
c.812_813del (p.Gly271AspfsTer20)
9g.134887316G>ACA5321382FCN2c.843G>A (p.Arg281=)
c.729G>A (p.Arg243=)
c.696G>A (p.Arg232=)
c.810G>A (p.Arg270=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.134887316G>CCA375461713FCN2c.843G>C (p.Arg281Ser)
c.729G>C (p.Arg243Ser)
c.696G>C (p.Arg232Ser)
c.810G>C (p.Arg270Ser)
9g.134887316G=CA1883419577FCN2c.843G= (p.Arg281=)
c.729G= (p.Arg243=)
c.696G= (p.Arg232=)
c.810G= (p.Arg270=)
9g.134887316G>TCA375461715FCN2c.843G>T (p.Arg281Ser)
c.729G>T (p.Arg243Ser)
c.696G>T (p.Arg232Ser)
c.810G>T (p.Arg270Ser)
 gnomAD v4
9g.134887317G>ACA375461723FCN2c.844G>A (p.Gly282Arg)
c.730G>A (p.Gly244Arg)
c.697G>A (p.Gly233Arg)
c.811G>A (p.Gly271Arg)
9g.134887317G>CCA375461721FCN2c.844G>C (p.Gly282Arg)
c.730G>C (p.Gly244Arg)
c.697G>C (p.Gly233Arg)
c.811G>C (p.Gly271Arg)
9g.134887317G>TCA375461718FCN2c.844G>T (p.Gly282Trp)
c.730G>T (p.Gly244Trp)
c.697G>T (p.Gly233Trp)
c.811G>T (p.Gly271Trp)
9g.134887318G>ACA375461725FCN2c.845G>A (p.Gly282Glu)
c.731G>A (p.Gly244Glu)
c.698G>A (p.Gly233Glu)
c.812G>A (p.Gly271Glu)
 gnomAD v4
9g.134887318G>CCA375461727FCN2c.845G>C (p.Gly282Ala)
c.731G>C (p.Gly244Ala)
c.698G>C (p.Gly233Ala)
c.812G>C (p.Gly271Ala)
 gnomAD v4
9g.134887318G>TCA375461729FCN2c.845G>T (p.Gly282Val)
c.731G>T (p.Gly244Val)
c.698G>T (p.Gly233Val)
c.812G>T (p.Gly271Val)
9g.134887318_134887319insTTTCA2741061248FCN2c.845_846insTTT (p.Gly282_Thr283insLeu)
c.731_732insTTT (p.Gly244_Thr245insLeu)
c.698_699insTTT (p.Gly233_Thr234insLeu)
c.812_813insTTT (p.Gly271_Thr272insLeu)
9g.134887319G>ACA201116464FCN2c.846G>A (p.Gly282=)
c.732G>A (p.Gly244=)
c.699G>A (p.Gly233=)
c.813G>A (p.Gly271=)
 dbSNP gnomAD v3 gnomAD v4 COSMIC
9g.134887319G>CCA467816444FCN2c.846G>C (p.Gly282=)
c.732G>C (p.Gly244=)
c.699G>C (p.Gly233=)
c.813G>C (p.Gly271=)
 dbSNP gnomAD v4
9g.134887319G=CA1883419578FCN2c.846G= (p.Gly282=)
c.732G= (p.Gly244=)
c.699G= (p.Gly233=)
c.813G= (p.Gly271=)
9g.134887319G>TCA467816445FCN2c.846G>T (p.Gly282=)
c.732G>T (p.Gly244=)
c.699G>T (p.Gly233=)
c.813G>T (p.Gly271=)
 dbSNP
9g.134887320A=CA1883419579FCN2c.847A= (p.Thr283=)
c.733A= (p.Thr245=)
c.700A= (p.Thr234=)
c.814A= (p.Thr272=)
9g.134887320A>CCA375461737FCN2c.847A>C (p.Thr283Pro)
c.733A>C (p.Thr245Pro)
c.700A>C (p.Thr234Pro)
c.814A>C (p.Thr272Pro)
9g.134887320A>GCA375461739FCN2c.847A>G (p.Thr283Ala)
c.733A>G (p.Thr245Ala)
c.700A>G (p.Thr234Ala)
c.814A>G (p.Thr272Ala)
9g.134887320A>TCA375461741FCN2c.847A>T (p.Thr283Ser)
c.733A>T (p.Thr245Ser)
c.700A>T (p.Thr234Ser)
c.814A>T (p.Thr272Ser)
 dbSNP gnomAD v4
9g.134887321C>ACA375461745FCN2c.848C>A (p.Thr283Asn)
c.734C>A (p.Thr245Asn)
c.701C>A (p.Thr234Asn)
c.815C>A (p.Thr272Asn)
9g.134887321C>GCA375461746FCN2c.848C>G (p.Thr283Ser)
c.734C>G (p.Thr245Ser)
c.701C>G (p.Thr234Ser)
c.815C>G (p.Thr272Ser)
9g.134887321C>TCA375461748FCN2c.848C>T (p.Thr283Ile)
c.734C>T (p.Thr245Ile)
c.701C>T (p.Thr234Ile)
c.815C>T (p.Thr272Ile)
9g.134887322T>ACA467816447FCN2c.849T>A (p.Thr283=)
c.735T>A (p.Thr245=)
c.702T>A (p.Thr234=)
c.816T>A (p.Thr272=)
9g.134887322T>CCA467816448FCN2c.849T>C (p.Thr283=)
c.735T>C (p.Thr245=)
c.702T>C (p.Thr234=)
c.816T>C (p.Thr272=)
 dbSNP gnomAD v3 gnomAD v4
9g.134887322T>GCA467816446FCN2c.849T>G (p.Thr283=)
c.735T>G (p.Thr245=)
c.702T>G (p.Thr234=)
c.816T>G (p.Thr272=)
9g.134887322T=CA1883419580FCN2c.849T= (p.Thr283=)
c.735T= (p.Thr245=)
c.702T= (p.Thr234=)
c.816T= (p.Thr272=)
9g.134887323C>ACA375461751FCN2c.850C>A (p.His284Asn)
c.736C>A (p.His246Asn)
c.703C>A (p.His235Asn)
c.817C>A (p.His273Asn)
9g.134887323C=CA1883419581FCN2c.850C= (p.His284=)
c.736C= (p.His246=)
c.703C= (p.His235=)
c.817C= (p.His273=)
9g.134887323C>GCA375461753FCN2c.850C>G (p.His284Asp)
c.736C>G (p.His246Asp)
c.703C>G (p.His235Asp)
c.817C>G (p.His273Asp)
 dbSNP gnomAD v2 gnomAD v4
9g.134887323C>TCA375461754FCN2c.850C>T (p.His284Tyr)
c.736C>T (p.His246Tyr)
c.703C>T (p.His235Tyr)
c.817C>T (p.His273Tyr)
9g.134887324A=CA1883419582FCN2c.851A= (p.His284=)
c.737A= (p.His246=)
c.704A= (p.His235=)
c.818A= (p.His273=)
9g.134887324A>CCA375461761FCN2c.851A>C (p.His284Pro)
c.737A>C (p.His246Pro)
c.704A>C (p.His235Pro)
c.818A>C (p.His273Pro)
 gnomAD v4
9g.134887324A>GCA375461757FCN2c.851A>G (p.His284Arg)
c.737A>G (p.His246Arg)
c.704A>G (p.His235Arg)
c.818A>G (p.His273Arg)
 COSMIC
9g.134887324A>TCA375461759FCN2c.851A>T (p.His284Leu)
c.737A>T (p.His246Leu)
c.704A>T (p.His235Leu)
c.818A>T (p.His273Leu)
9g.134887325T>ACA375461764FCN2c.852T>A (p.His284Gln)
c.738T>A (p.His246Gln)
c.705T>A (p.His235Gln)
c.819T>A (p.His273Gln)
9g.134887325T>CCA5321383FCN2c.852T>C (p.His284=)
c.738T>C (p.His246=)
c.705T>C (p.His235=)
c.819T>C (p.His273=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.134887325T>GCA375461768FCN2c.852T>G (p.His284Gln)
c.738T>G (p.His246Gln)
c.705T>G (p.His235Gln)
c.819T>G (p.His273Gln)
9g.134887325T=CA1883419583FCN2c.852T= (p.His284=)
c.738T= (p.His246=)
c.705T= (p.His235=)
c.819T= (p.His273=)
9g.134887325dupCA591363753FCN2c.852dup (p.Gly285TrpfsTer18)
c.738dup (p.Gly247TrpfsTer18)
c.705dup (p.Gly236TrpfsTer18)
c.819dup (p.Gly274TrpfsTer18)
 dbSNP gnomAD v2
9g.134887326G>ACA375461771FCN2c.853G>A (p.Gly285Ser)
c.739G>A (p.Gly247Ser)
c.706G>A (p.Gly236Ser)
c.820G>A (p.Gly274Ser)
 dbSNP COSMIC
9g.134887326G>CCA375461772FCN2c.853G>C (p.Gly285Arg)
c.739G>C (p.Gly247Arg)
c.706G>C (p.Gly236Arg)
c.820G>C (p.Gly274Arg)
9g.134887326G=CA1883419584FCN2c.853G= (p.Gly285=)
c.739G= (p.Gly247=)
c.706G= (p.Gly236=)
c.820G= (p.Gly274=)
9g.134887326G>TCA375461774FCN2c.853G>T (p.Gly285Cys)
c.739G>T (p.Gly247Cys)
c.706G>T (p.Gly236Cys)
c.820G>T (p.Gly274Cys)
9g.134887327G>ACA375461776FCN2c.854G>A (p.Gly285Asp)
c.740G>A (p.Gly247Asp)
c.707G>A (p.Gly236Asp)
c.821G>A (p.Gly274Asp)
 dbSNP gnomAD v3 gnomAD v4
9g.134887327G>CCA375461778FCN2c.854G>C (p.Gly285Ala)
c.740G>C (p.Gly247Ala)
c.707G>C (p.Gly236Ala)
c.821G>C (p.Gly274Ala)
9g.134887327G=CA1883419585FCN2c.854G= (p.Gly285=)
c.740G= (p.Gly247=)
c.707G= (p.Gly236=)
c.821G= (p.Gly274=)
9g.134887327G>TCA375461781FCN2c.854G>T (p.Gly285Val)
c.740G>T (p.Gly247Val)
c.707G>T (p.Gly236Val)
c.821G>T (p.Gly274Val)
9g.134887328C>ACA467816449FCN2c.855C>A (p.Gly285=)
c.741C>A (p.Gly247=)
c.708C>A (p.Gly236=)
c.822C>A (p.Gly274=)
9g.134887328C>GCA467816450FCN2c.855C>G (p.Gly285=)
c.741C>G (p.Gly247=)
c.708C>G (p.Gly236=)
c.822C>G (p.Gly274=)
9g.134887328C>TCA467816451FCN2c.855C>T (p.Gly285=)
c.741C>T (p.Gly247=)
c.708C>T (p.Gly236=)
c.822C>T (p.Gly274=)
9g.134887329A>CCA375461784FCN2c.856A>C (p.Ser286Arg)
c.742A>C (p.Ser248Arg)
c.709A>C (p.Ser237Arg)
c.823A>C (p.Ser275Arg)
9g.134887329A>GCA375461787FCN2c.856A>G (p.Ser286Gly)
c.742A>G (p.Ser248Gly)
c.709A>G (p.Ser237Gly)
c.823A>G (p.Ser275Gly)
9g.134887329A>TCA375461789FCN2c.856A>T (p.Ser286Cys)
c.742A>T (p.Ser248Cys)
c.709A>T (p.Ser237Cys)
c.823A>T (p.Ser275Cys)
9g.134887330G>ACA375461794FCN2c.857G>A (p.Ser286Asn)
c.743G>A (p.Ser248Asn)
c.710G>A (p.Ser237Asn)
c.824G>A (p.Ser275Asn)
9g.134887330G>CCA375461797FCN2c.857G>C (p.Ser286Thr)
c.743G>C (p.Ser248Thr)
c.710G>C (p.Ser237Thr)
c.824G>C (p.Ser275Thr)
9g.134887330G>TCA375461792FCN2c.857G>T (p.Ser286Ile)
c.743G>T (p.Ser248Ile)
c.710G>T (p.Ser237Ile)
c.824G>T (p.Ser275Ile)
9g.134887331C>ACA375461802FCN2c.858C>A (p.Ser286Arg)
c.744C>A (p.Ser248Arg)
c.711C>A (p.Ser237Arg)
c.825C>A (p.Ser275Arg)
9g.134887331C=CA1883419586FCN2c.858C= (p.Ser286=)
c.744C= (p.Ser248=)
c.711C= (p.Ser237=)
c.825C= (p.Ser275=)
9g.134887331C>GCA375461800FCN2c.858C>G (p.Ser286Arg)
c.744C>G (p.Ser248Arg)
c.711C>G (p.Ser237Arg)
c.825C>G (p.Ser275Arg)
9g.134887331C>TCA467816452FCN2c.858C>T (p.Ser286=)
c.744C>T (p.Ser248=)
c.711C>T (p.Ser237=)
c.825C>T (p.Ser275=)
 dbSNP gnomAD v4
9g.134887332T>ACA375461805FCN2c.859T>A (p.Phe287Ile)
c.745T>A (p.Phe249Ile)
c.712T>A (p.Phe238Ile)
c.826T>A (p.Phe276Ile)
9g.134887332T>CCA375461808FCN2c.859T>C (p.Phe287Leu)
c.745T>C (p.Phe249Leu)
c.712T>C (p.Phe238Leu)
c.826T>C (p.Phe276Leu)
9g.134887332T>GCA375461810FCN2c.859T>G (p.Phe287Val)
c.745T>G (p.Phe249Val)
c.712T>G (p.Phe238Val)
c.826T>G (p.Phe276Val)
9g.134887333T>ACA375461813FCN2c.860T>A (p.Phe287Tyr)
c.746T>A (p.Phe249Tyr)
c.713T>A (p.Phe238Tyr)
c.827T>A (p.Phe276Tyr)
9g.134887333T>CCA375461815FCN2c.860T>C (p.Phe287Ser)
c.746T>C (p.Phe249Ser)
c.713T>C (p.Phe238Ser)
c.827T>C (p.Phe276Ser)
 dbSNP gnomAD v3 gnomAD v4
9g.134887333T>GCA375461816FCN2c.860T>G (p.Phe287Cys)
c.746T>G (p.Phe249Cys)
c.713T>G (p.Phe238Cys)
c.827T>G (p.Phe276Cys)
9g.134887333T=CA1883419587FCN2c.860T= (p.Phe287=)
c.746T= (p.Phe249=)
c.713T= (p.Phe238=)
c.827T= (p.Phe276=)
9g.134887334T>ACA375461819FCN2c.861T>A (p.Phe287Leu)
c.747T>A (p.Phe249Leu)
c.714T>A (p.Phe238Leu)
c.828T>A (p.Phe276Leu)
9g.134887334T>CCA467816453FCN2c.861T>C (p.Phe287=)
c.747T>C (p.Phe249=)
c.714T>C (p.Phe238=)
c.828T>C (p.Phe276=)
9g.134887334T>GCA375461821FCN2c.861T>G (p.Phe287Leu)
c.747T>G (p.Phe249Leu)
c.714T>G (p.Phe238Leu)
c.828T>G (p.Phe276Leu)
9g.134887335G>ACA375461824FCN2c.862G>A (p.Ala288Thr)
c.748G>A (p.Ala250Thr)
c.715G>A (p.Ala239Thr)
c.829G>A (p.Ala277Thr)
9g.134887335G>CCA375461826FCN2c.862G>C (p.Ala288Pro)
c.748G>C (p.Ala250Pro)
c.715G>C (p.Ala239Pro)
c.829G>C (p.Ala277Pro)
9g.134887335G>TCA375461829FCN2c.862G>T (p.Ala288Ser)
c.748G>T (p.Ala250Ser)
c.715G>T (p.Ala239Ser)
c.829G>T (p.Ala277Ser)
9g.134887336C>ACA375461835FCN2c.863C>A (p.Ala288Glu)
c.749C>A (p.Ala250Glu)
c.716C>A (p.Ala239Glu)
c.830C>A (p.Ala277Glu)
9g.134887336C>GCA375461831FCN2c.863C>G (p.Ala288Gly)
c.749C>G (p.Ala250Gly)
c.716C>G (p.Ala239Gly)
c.830C>G (p.Ala277Gly)
 COSMIC
9g.134887336C>TCA375461833FCN2c.863C>T (p.Ala288Val)
c.749C>T (p.Ala250Val)
c.716C>T (p.Ala239Val)
c.830C>T (p.Ala277Val)
9g.134887337A=CA1883419588FCN2c.864A= (p.Ala288=)
c.750A= (p.Ala250=)
c.717A= (p.Ala239=)
c.831A= (p.Ala277=)
9g.134887337A>CCA467816456FCN2c.864A>C (p.Ala288=)
c.750A>C (p.Ala250=)
c.717A>C (p.Ala239=)
c.831A>C (p.Ala277=)
9g.134887337A>GCA467816454FCN2c.864A>G (p.Ala288=)
c.750A>G (p.Ala250=)
c.717A>G (p.Ala239=)
c.831A>G (p.Ala277=)
 dbSNP
9g.134887337A>TCA467816455FCN2c.864A>T (p.Ala288=)
c.750A>T (p.Ala250=)
c.717A>T (p.Ala239=)
c.831A>T (p.Ala277=)
9g.134887338A>CCA375461837FCN2c.865A>C (p.Asn289His)
c.751A>C (p.Asn251His)
c.718A>C (p.Asn240His)
c.832A>C (p.Asn278His)
9g.134887338A>GCA375461838FCN2c.865A>G (p.Asn289Asp)
c.751A>G (p.Asn251Asp)
c.718A>G (p.Asn240Asp)
c.832A>G (p.Asn278Asp)
9g.134887338A>TCA375461840FCN2c.865A>T (p.Asn289Tyr)
c.751A>T (p.Asn251Tyr)
c.718A>T (p.Asn240Tyr)
c.832A>T (p.Asn278Tyr)
9g.134887339A=CA1883419589FCN2c.866A= (p.Asn289=)
c.752A= (p.Asn251=)
c.719A= (p.Asn240=)
c.833A= (p.Asn278=)
9g.134887339A>CCA375461844FCN2c.866A>C (p.Asn289Thr)
c.752A>C (p.Asn251Thr)
c.719A>C (p.Asn240Thr)
c.833A>C (p.Asn278Thr)
 dbSNP gnomAD v2 gnomAD v4
9g.134887339A>GCA375461846FCN2c.866A>G (p.Asn289Ser)
c.752A>G (p.Asn251Ser)
c.719A>G (p.Asn240Ser)
c.833A>G (p.Asn278Ser)
9g.134887339A>TCA375461849FCN2c.866A>T (p.Asn289Ile)
c.752A>T (p.Asn251Ile)
c.719A>T (p.Asn240Ile)
c.833A>T (p.Asn278Ile)
9g.134887340T>ACA375461852FCN2c.867T>A (p.Asn289Lys)
c.753T>A (p.Asn251Lys)
c.720T>A (p.Asn240Lys)
c.834T>A (p.Asn278Lys)
 dbSNP gnomAD v3 gnomAD v4
9g.134887340T>CCA5321384FCN2c.867T>C (p.Asn289=)
c.753T>C (p.Asn251=)
c.720T>C (p.Asn240=)
c.834T>C (p.Asn278=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.134887340T>GCA375461857FCN2c.867T>G (p.Asn289Lys)
c.753T>G (p.Asn251Lys)
c.720T>G (p.Asn240Lys)
c.834T>G (p.Asn278Lys)
9g.134887340T=CA1883419590FCN2c.867T= (p.Asn289=)
c.753T= (p.Asn251=)
c.720T= (p.Asn240=)
c.834T= (p.Asn278=)
9g.134887341G>ACA375461860FCN2c.868G>A (p.Gly290Ser)
c.754G>A (p.Gly252Ser)
c.721G>A (p.Gly241Ser)
c.835G>A (p.Gly279Ser)
 dbSNP gnomAD v3 gnomAD v4
9g.134887341G>CCA375461862FCN2c.868G>C (p.Gly290Arg)
c.754G>C (p.Gly252Arg)
c.721G>C (p.Gly241Arg)
c.835G>C (p.Gly279Arg)
9g.134887341G=CA1883419591FCN2c.868G= (p.Gly290=)
c.754G= (p.Gly252=)
c.721G= (p.Gly241=)
c.835G= (p.Gly279=)
9g.134887341G>TCA375461864FCN2c.868G>T (p.Gly290Cys)
c.754G>T (p.Gly252Cys)
c.721G>T (p.Gly241Cys)
c.835G>T (p.Gly279Cys)
9g.134887342G>ACA375461870FCN2c.869G>A (p.Gly290Asp)
c.755G>A (p.Gly252Asp)
c.722G>A (p.Gly241Asp)
c.836G>A (p.Gly279Asp)
9g.134887342G>CCA375461872FCN2c.869G>C (p.Gly290Ala)
c.755G>C (p.Gly252Ala)
c.722G>C (p.Gly241Ala)
c.836G>C (p.Gly279Ala)
 dbSNP gnomAD v4
9g.134887342G=CA1883419592FCN2c.869G= (p.Gly290=)
c.755G= (p.Gly252=)
c.722G= (p.Gly241=)
c.836G= (p.Gly279=)
9g.134887342G>TCA375461868FCN2c.869G>T (p.Gly290Val)
c.755G>T (p.Gly252Val)
c.722G>T (p.Gly241Val)
c.836G>T (p.Gly279Val)
 gnomAD v4
9g.134887343C>ACA467816459FCN2c.870C>A (p.Gly290=)
c.756C>A (p.Gly252=)
c.723C>A (p.Gly241=)
c.837C>A (p.Gly279=)
9g.134887343C>GCA467816458FCN2c.870C>G (p.Gly290=)
c.756C>G (p.Gly252=)
c.723C>G (p.Gly241=)
c.837C>G (p.Gly279=)
9g.134887343C>TCA467816457FCN2c.870C>T (p.Gly290=)
c.756C>T (p.Gly252=)
c.723C>T (p.Gly241=)
c.837C>T (p.Gly279=)
 gnomAD v4
9g.134887344A=CA1883419593FCN2c.871A= (p.Ile291=)
c.757A= (p.Ile253=)
c.724A= (p.Ile242=)
c.838A= (p.Ile280=)
9g.134887344A>CCA201116491FCN2c.871A>C (p.Ile291Leu)
c.757A>C (p.Ile253Leu)
c.724A>C (p.Ile242Leu)
c.838A>C (p.Ile280Leu)
 dbSNP gnomAD v3 gnomAD v4
9g.134887344A>GCA375461876FCN2c.871A>G (p.Ile291Val)
c.757A>G (p.Ile253Val)
c.724A>G (p.Ile242Val)
c.838A>G (p.Ile280Val)
9g.134887344A>TCA375461879FCN2c.871A>T (p.Ile291Phe)
c.757A>T (p.Ile253Phe)
c.724A>T (p.Ile242Phe)
c.838A>T (p.Ile280Phe)
9g.134887345T>ACA375461882FCN2c.872T>A (p.Ile291Asn)
c.758T>A (p.Ile253Asn)
c.725T>A (p.Ile242Asn)
c.839T>A (p.Ile280Asn)
9g.134887345T>CCA375461884FCN2c.872T>C (p.Ile291Thr)
c.758T>C (p.Ile253Thr)
c.725T>C (p.Ile242Thr)
c.839T>C (p.Ile280Thr)
9g.134887345T>GCA375461886FCN2c.872T>G (p.Ile291Ser)
c.758T>G (p.Ile253Ser)
c.725T>G (p.Ile242Ser)
c.839T>G (p.Ile280Ser)

Number of alleles fetched