Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.240878045C>ACA432026170AGXTc.966C>A (p.Thr322=)
n.744C>A
2g.240878045C>GCA432026172AGXTc.966C>G (p.Thr322=)
n.744C>G
2g.240878045C>TCA432026173AGXTc.966C>T (p.Thr322=)
n.744C>T
dbSNP
2g.240878046A>CCA351319498AGXTc.967A>C (p.Thr323Pro)
n.745A>C
2g.240878046A>GCA351319499AGXTc.967A>G (p.Thr323Ala)
n.745A>G
2g.240878046A>TCA351319500AGXTc.967A>T (p.Thr323Ser)
n.745A>T
2g.240878047C>ACA351319502AGXTc.968C>A (p.Thr323Asn)
n.746C>A
2g.240878047C>GCA351319503AGXTc.968C>G (p.Thr323Ser)
n.746C>G
2g.240878047C>TCA351319501AGXTc.968C>T (p.Thr323Ile)
n.746C>T
gnomAD v4
2g.240878047_240878049delinsCTGCA1339335761AGXTc.968_970delinsCTG (p.Thr323=)
n.746_748delinsCTG
2g.240878048T>ACA432026185AGXTc.969T>A (p.Thr323=)
n.747T>A
2g.240878048T>CCA432026186AGXTc.969T>C (p.Thr323=)
n.747T>C
2g.240878048T>GCA432026188AGXTc.969T>G (p.Thr323=)
n.747T>G
2g.240878050_240878051delCA275862AGXTc.971_972del (p.Val324GlyfsTer7)
n.749_750del
ClinVar dbSNP
2g.240878049G>ACA351319504AGXTc.970G>A (p.Val324Met)
n.748G>A
2g.240878049G>CCA351319505AGXTc.970G>C (p.Val324Leu)
n.748G>C
2g.240878049G>TCA351319506AGXTc.970G>T (p.Val324Leu)
n.748G>T
2g.240878050T>ACA351319507AGXTc.971T>A (p.Val324Glu)
n.749T>A
2g.240878050T>CCA351319508AGXTc.971T>C (p.Val324Ala)
n.749T>C
dbSNP gnomAD v2 gnomAD v4
2g.240878050T>GCA351319509AGXTc.971T>G (p.Val324Gly)
n.749T>G
gnomAD v4
2g.240878050T=CA1339335762AGXTc.971T= (p.Val324=)
n.749T=
2g.240878050_240878051delinsTGCA1339335763AGXTc.971_972delinsTG (p.Val324=)
n.749_750delinsTG
2g.240878051G>ACA432026199AGXTc.972G>A (p.Val324=)
n.750G>A
ClinVar
2g.240878051G>CCA432026195AGXTc.972G>C (p.Val324=)
n.750G>C
2g.240878051G>TCA432026198AGXTc.972G>T (p.Val324=)
n.750G>T
2g.240878052delCA1139655794AGXTc.973del (p.Ala325LeufsTer16)
n.751del
ClinVar dbSNP
2g.240878052G>ACA2209365AGXTc.973G>A (p.Ala325Thr)
n.751G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.240878052G>CCA351319510AGXTc.973G>C (p.Ala325Pro)
n.751G>C
2g.240878052G=CA1339335764AGXTc.973G= (p.Ala325=)
n.751G=
2g.240878052G>TCA351319511AGXTc.973G>T (p.Ala325Ser)
n.751G>T
2g.240878053C>ACA351319512AGXTc.974C>A (p.Ala325Asp)
n.752C>A
2g.240878053C>GCA351319513AGXTc.974C>G (p.Ala325Gly)
n.752C>G
2g.240878053C>TCA351319514AGXTc.974C>T (p.Ala325Val)
n.752C>T
gnomAD v4
2g.240878054T>ACA432026201AGXTc.975T>A (p.Ala325=)
n.753T>A
2g.240878054T>CCA432026202AGXTc.975T>C (p.Ala325=)
n.753T>C
ClinVar
2g.240878054T>GCA432026203AGXTc.975T>G (p.Ala325=)
n.753T>G
2g.240878054_240878055delinsTGCA1339335765AGXTc.975_976delinsTG (p.Ala325=)
n.753_754delinsTG
2g.240878055delCA274440AGXTc.976del (p.Val326TyrfsTer15)
n.754del
ClinVar dbSNP gnomAD v2 gnomAD v4
2g.240878055G>ACA275602AGXTc.976G>A (p.Val326Ile)
n.754G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.240878055G>CCA351319515AGXTc.976G>C (p.Val326Leu)
n.754G>C
2g.240878055G=CA1339335766AGXTc.976G= (p.Val326=)
n.754G=
2g.240878055G>TCA351319516AGXTc.976G>T (p.Val326Leu)
n.754G>T
gnomAD v4
2g.240878056delCA351319520AGXTc.977del (p.Val326AspfsTer15)
n.755del
2g.240878056T>ACA351319517AGXTc.977T>A (p.Val326Glu)
n.755T>A
2g.240878056T>CCA351319518AGXTc.977T>C (p.Val326Ala)
n.755T>C
dbSNP gnomAD v3 gnomAD v4
2g.240878056T>GCA351319519AGXTc.977T>G (p.Val326Gly)
n.755T>G
2g.240878056T=CA1339335767AGXTc.977T= (p.Val326=)
n.755T=
2g.240878057A>CCA432026213AGXTc.978A>C (p.Val326=)
n.756A>C
2g.240878057A>GCA432026215AGXTc.978A>G (p.Val326=)
n.756A>G
2g.240878057A>TCA432026216AGXTc.978A>T (p.Val326=)
n.756A>T
ClinVar dbSNP
2g.240878058C>ACA351319521AGXTc.979C>A (p.Pro327Thr)
n.757C>A
2g.240878058C=CA1339335768AGXTc.979C= (p.Pro327=)
n.757C=
2g.240878058C>GCA351319522AGXTc.979C>G (p.Pro327Ala)
n.757C>G
2g.240878058C>TCA351319523AGXTc.979C>T (p.Pro327Ser)
n.757C>T
dbSNP
2g.240878059C>ACA351319524AGXTc.980C>A (p.Pro327His)
n.758C>A
2g.240878059C>GCA351319525AGXTc.980C>G (p.Pro327Arg)
n.758C>G
2g.240878059C>TCA351319526AGXTc.980C>T (p.Pro327Leu)
n.758C>T
2g.240878060C>ACA432026222AGXTc.981C>A (p.Pro327=)
n.759C>A
gnomAD v4
2g.240878060C=CA1339335769AGXTc.981C= (p.Pro327=)
n.759C=
2g.240878060C>GCA432026224AGXTc.981C>G (p.Pro327=)
n.759C>G
2g.240878060C>TCA2209366AGXTc.981C>T (p.Pro327=)
n.759C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.240878061G>ACA2209367AGXTc.982G>A (p.Ala328Thr)
n.760G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.240878061G>CCA351319528AGXTc.982G>C (p.Ala328Pro)
n.760G>C
dbSNP
2g.240878061G=CA1339335771AGXTc.982G= (p.Ala328=)
n.760G=
2g.240878061G>TCA351319527AGXTc.982G>T (p.Ala328Ser)
n.760G>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.240878061_240878067delinsGCTGGCTCA1339335770AGXTc.982_988delinsGCTGGCT (p.Ala328=)
n.760_766delinsGCTGGCT
2g.240878062C>ACA351319529AGXTc.983C>A (p.Ala328Asp)
n.761C>A
2g.240878062C>GCA351319530AGXTc.983C>G (p.Ala328Gly)
n.761C>G
2g.240878062C>TCA351319531AGXTc.983C>T (p.Ala328Val)
n.761C>T
2g.240878062dupCA2580068044AGXTc.983dup (p.Gly329TrpfsTer3)
n.761dup
ClinVar
2g.240878062_240878067delCA275863AGXTc.983_988del (p.Ala328_Tyr330delinsAsp)
n.761_766del
ClinVar dbSNP
2g.240878063T>ACA432026227AGXTc.984T>A (p.Ala328=)
n.762T>A
2g.240878063T>CCA432026229AGXTc.984T>C (p.Ala328=)
n.762T>C
ClinVar
2g.240878063T>GCA432026231AGXTc.984T>G (p.Ala328=)
n.762T>G
ClinVar dbSNP gnomAD v4
2g.240878063T=CA1339335772AGXTc.984T= (p.Ala328=)
n.762T=
2g.240878064G>ACA2209368AGXTc.985G>A (p.Gly329Ser)
n.763G>A
dbSNP ExAC gnomAD v2 gnomAD v4
2g.240878064G>CCA351319532AGXTc.985G>C (p.Gly329Arg)
n.763G>C
2g.240878064G=CA1339335773AGXTc.985G= (p.Gly329=)
n.763G=
2g.240878064G>TCA351319533AGXTc.985G>T (p.Gly329Cys)
n.763G>T
2g.240878065G>ACA351319534AGXTc.986G>A (p.Gly329Asp)
n.764G>A
2g.240878065G>CCA351319535AGXTc.986G>C (p.Gly329Ala)
n.764G>C
2g.240878065G>TCA351319536AGXTc.986G>T (p.Gly329Val)
n.764G>T
2g.240878066C>ACA432026240AGXTc.987C>A (p.Gly329=)
n.765C>A
2g.240878066C=CA1339335774AGXTc.987C= (p.Gly329=)
n.765C=
2g.240878066C>GCA68180834AGXTc.987C>G (p.Gly329=)
n.765C>G
dbSNP
2g.240878066C>TCA2209369AGXTc.987C>T (p.Gly329=)
n.765C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.240878067T>ACA351319539AGXTc.988T>A (p.Tyr330Asn)
n.766T>A
2g.240878067T>CCA351319537AGXTc.988T>C (p.Tyr330His)
n.766T>C
2g.240878067T>GCA351319538AGXTc.988T>G (p.Tyr330Asp)
n.766T>G
2g.240878068A=CA1339335775AGXTc.989A= (p.Tyr330=)
n.767A=
2g.240878068A>CCA351319540AGXTc.989A>C (p.Tyr330Ser)
n.767A>C
2g.240878068A>GCA351319541AGXTc.989A>G (p.Tyr330Cys)
n.767A>G
dbSNP gnomAD v3 gnomAD v4
2g.240878068A>TCA351319542AGXTc.989A>T (p.Tyr330Phe)
n.767A>T
2g.240878069T>ACA351319543AGXTc.990T>A (p.Tyr330Ter)
n.768T>A
2g.240878069T>CCA432026243AGXTc.990T>C (p.Tyr330=)
n.768T>C
dbSNP gnomAD v3 gnomAD v4
2g.240878069T>GCA68180837AGXTc.990T>G (p.Tyr330Ter)
n.768T>G
dbSNP
2g.240878069T=CA1339335776AGXTc.990T= (p.Tyr330=)
n.768T=
2g.240878070G>ACA351319544AGXTc.991G>A (p.Asp331Asn)
n.769G>A
2g.240878070G>CCA351319546AGXTc.991G>C (p.Asp331His)
n.769G>C
2g.240878070G>TCA351319545AGXTc.991G>T (p.Asp331Tyr)
n.769G>T
gnomAD v4
2g.240878071A>CCA351319547AGXTc.992A>C (p.Asp331Ala)
n.770A>C
2g.240878071A>GCA351319548AGXTc.992A>G (p.Asp331Gly)
n.770A>G
2g.240878071A>TCA351319549AGXTc.992A>T (p.Asp331Val)
n.770A>T
2g.240878072C>ACA351319550AGXTc.993C>A (p.Asp331Glu)
n.771C>A
2g.240878072C>GCA351319551AGXTc.993C>G (p.Asp331Glu)
n.771C>G
2g.240878072C>TCA432026256AGXTc.993C>T (p.Asp331=)
n.771C>T
gnomAD v4
2g.240878073T>ACA351319552AGXTc.994T>A (p.Trp332Arg)
n.772T>A
2g.240878073T>CCA351319553AGXTc.994T>C (p.Trp332Arg)
n.772T>C
2g.240878073T>GCA351319554AGXTc.994T>G (p.Trp332Gly)
n.772T>G
2g.240878073_240878074delCA2695197712AGXTc.994_995del (p.Trp332GlufsTer14)
n.772_773del
ClinVar
2g.240878074G>ACA351319555AGXTc.995G>A (p.Trp332Ter)
n.773G>A
gnomAD v4
2g.240878074G>CCA351319556AGXTc.995G>C (p.Trp332Ser)
n.773G>C
2g.240878074G>TCA351319557AGXTc.995G>T (p.Trp332Leu)
n.773G>T
2g.240878075G>ACA275769AGXTc.996G>A (p.Trp332Ter)
n.774G>A
ClinVar dbSNP gnomAD v4
2g.240878075G>CCA68180843AGXTc.996G>C (p.Trp332Cys)
n.774G>C
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.240878075G=CA1339335777AGXTc.996G= (p.Trp332=)
n.774G=
2g.240878075G>TCA351319558AGXTc.996G>T (p.Trp332Cys)
n.774G>T
2g.240878076A=CA1339335778AGXTc.997A= (p.Arg333=)
n.775A=
2g.240878076A>CCA432026262AGXTc.997A>C (p.Arg333=)
n.775A>C
ClinVar dbSNP gnomAD v2 gnomAD v4
2g.240878076A>GCA351319559AGXTc.997A>G (p.Arg333Gly)
n.775A>G
2g.240878076A>TCA275772AGXTc.997A>T (p.Arg333Ter)
n.775A>T
ClinVar dbSNP
2g.240878077G>ACA351319560AGXTc.998G>A (p.Arg333Lys)
n.776G>A
2g.240878077G>CCA351319561AGXTc.998G>C (p.Arg333Thr)
n.776G>C
2g.240878077G>TCA351319562AGXTc.998G>T (p.Arg333Ile)
n.776G>T
gnomAD v4
2g.240878078A>CCA351319563AGXTc.999A>C (p.Arg333Ser)
n.777A>C
2g.240878078A>GCA432026269AGXTc.999A>G (p.Arg333=)
n.777A>G
2g.240878078A>TCA351319564AGXTc.999A>T (p.Arg333Ser)
n.777A>T
2g.240878079G>ACA2209370AGXTc.1000G>A (p.Asp334Asn)
n.778G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.240878079G>CCA351319565AGXTc.1000G>C (p.Asp334His)
n.778G>C
dbSNP
2g.240878079G=CA1339335779AGXTc.1000G= (p.Asp334=)
n.778G=
2g.240878079G>TCA351319566AGXTc.1000G>T (p.Asp334Tyr)
n.778G>T
2g.240878080A=CA1339335780AGXTc.1001A= (p.Asp334=)
n.779A=
2g.240878080A>CCA351319567AGXTc.1001A>C (p.Asp334Ala)
n.779A>C
2g.240878080A>GCA2209371AGXTc.1001A>G (p.Asp334Gly)
n.779A>G
dbSNP ExAC gnomAD v2 gnomAD v4
2g.240878080A>TCA351319568AGXTc.1001A>T (p.Asp334Val)
n.779A>T
2g.240878081C>ACA351319569AGXTc.1002C>A (p.Asp334Glu)
n.780C>A
2g.240878081C=CA1339335781AGXTc.1002C= (p.Asp334=)
n.780C=
2g.240878081C>GCA351319570AGXTc.1002C>G (p.Asp334Glu)
n.780C>G
2g.240878081C>TCA2209372AGXTc.1002C>T (p.Asp334=)
n.780C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.240878082A>CCA351319571AGXTc.1003A>C (p.Ile335Leu)
n.781A>C
2g.240878082A>GCA351319572AGXTc.1003A>G (p.Ile335Val)
n.781A>G
2g.240878082A>TCA351319573AGXTc.1003A>T (p.Ile335Phe)
n.781A>T
2g.240878083T>ACA351319574AGXTc.1004T>A (p.Ile335Asn)
n.782T>A
2g.240878083T>CCA351319575AGXTc.1004T>C (p.Ile335Thr)
n.782T>C
2g.240878083T>GCA351319576AGXTc.1004T>G (p.Ile335Ser)
n.782T>G
2g.240878084C>ACA432026287AGXTc.1005C>A (p.Ile335=)
n.783C>A
gnomAD v4
2g.240878084C=CA1339335782AGXTc.1005C= (p.Ile335=)
n.783C=
2g.240878084C>GCA351319577AGXTc.1005C>G (p.Ile335Met)
n.783C>G
2g.240878084C>TCA432026288AGXTc.1005C>T (p.Ile335=)
n.783C>T
ClinVar dbSNP gnomAD v2 gnomAD v4
2g.240878085G>ACA2209373AGXTc.1006G>A (p.Val336Ile)
n.784G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
2g.240878085G>CCA351319578AGXTc.1006G>C (p.Val336Leu)
n.784G>C
2g.240878085G=CA1339335783AGXTc.1006G= (p.Val336=)
n.784G=
2g.240878085G>TCA351319579AGXTc.1006G>T (p.Val336Phe)
n.784G>T
2g.240878086T>ACA275775AGXTc.1007T>A (p.Val336Asp)
n.785T>A
ClinVar dbSNP gnomAD v2 gnomAD v4
2g.240878086T>CCA351319581AGXTc.1007T>C (p.Val336Ala)
n.785T>C
dbSNP
2g.240878086T>GCA351319580AGXTc.1007T>G (p.Val336Gly)
n.785T>G
2g.240878086T=CA1339335784AGXTc.1007T= (p.Val336=)
n.785T=
2g.240878087C>ACA432026299AGXTc.1008C>A (p.Val336=)
n.786C>A
dbSNP
2g.240878087C=CA1339335785AGXTc.1008C= (p.Val336=)
n.786C=
2g.240878087C>GCA432026301AGXTc.1008C>G (p.Val336=)
n.786C>G
2g.240878087C>TCA432026297AGXTc.1008C>T (p.Val336=)
n.786C>T
2g.240878088A>CCA351319584AGXTc.1009A>C (p.Ser337Arg)
n.787A>C
2g.240878088A>GCA351319582AGXTc.1009A>G (p.Ser337Gly)
n.787A>G
2g.240878088A>TCA351319583AGXTc.1009A>T (p.Ser337Cys)
n.787A>T
2g.240878089G>ACA351319585AGXTc.1010G>A (p.Ser337Asn)
n.788G>A
2g.240878089G>CCA351319586AGXTc.1010G>C (p.Ser337Thr)
n.788G>C
2g.240878089G>TCA351319587AGXTc.1010G>T (p.Ser337Ile)
n.788G>T
2g.240878090C>ACA351319588AGXTc.1011C>A (p.Ser337Arg)
n.789C>A
2g.240878090C>GCA351319589AGXTc.1011C>G (p.Ser337Arg)
n.789C>G
2g.240878090C>TCA432026311AGXTc.1011C>T (p.Ser337=)
n.789C>T
2g.240878091T>ACA351319590AGXTc.1012T>A (p.Tyr338Asn)
n.790T>A
dbSNP
2g.240878091T>CCA351319591AGXTc.1012T>C (p.Tyr338His)
n.790T>C
2g.240878091T>GCA351319592AGXTc.1012T>G (p.Tyr338Asp)
n.790T>G
2g.240878091T=CA1339335786AGXTc.1012T= (p.Tyr338=)
n.790T=
2g.240878092A=CA1339335787AGXTc.1013A= (p.Tyr338=)
n.791A=
2g.240878092A>CCA351319593AGXTc.1013A>C (p.Tyr338Ser)
n.791A>C
2g.240878092A>GCA351319594AGXTc.1013A>G (p.Tyr338Cys)
n.791A>G
2g.240878092A>TCA2209374AGXTc.1013A>T (p.Tyr338Phe)
n.791A>T
dbSNP ExAC gnomAD v2 gnomAD v4
2g.240878093C>ACA351319595AGXTc.1014C>A (p.Tyr338Ter)
n.792C>A
ClinVar
2g.240878093C=CA1339335788AGXTc.1014C= (p.Tyr338=)
n.792C=
2g.240878093C>GCA275776AGXTc.1014C>G (p.Tyr338Ter)
n.792C>G
ClinVar dbSNP
2g.240878093C>TCA2209375AGXTc.1014C>T (p.Tyr338=)
n.792C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.240878094delCA2586971646AGXTc.1015del (p.Val339SerfsTer2)
n.793del
2g.240878094G>ACA2209376AGXTc.1015G>A (p.Val339Ile)
n.793G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.240878094G>CCA351319596AGXTc.1015G>C (p.Val339Leu)
n.793G>C
2g.240878094G=CA1339335789AGXTc.1015G= (p.Val339=)
n.793G=
2g.240878094G>TCA351319597AGXTc.1015G>T (p.Val339Phe)
n.793G>T
2g.240878095T>ACA351319598AGXTc.1016T>A (p.Val339Asp)
n.794T>A
2g.240878095T>CCA351319599AGXTc.1016T>C (p.Val339Ala)
n.794T>C
gnomAD v4
2g.240878095T>GCA351319600AGXTc.1016T>G (p.Val339Gly)
n.794T>G
2g.240878096C>ACA432026326AGXTc.1017C>A (p.Val339=)
n.795C>A
2g.240878096C>GCA432026328AGXTc.1017C>G (p.Val339=)
n.795C>G
2g.240878096C>TCA432026329AGXTc.1017C>T (p.Val339=)
n.795C>T
gnomAD v4
2g.240878097A>CCA351319601AGXTc.1018A>C (p.Ile340Leu)
n.796A>C
2g.240878097A>GCA351319602AGXTc.1018A>G (p.Ile340Val)
n.796A>G
2g.240878097A>TCA351319603AGXTc.1018A>T (p.Ile340Leu)
n.796A>T
2g.240878098T>ACA351319604AGXTc.1019T>A (p.Ile340Lys)
n.797T>A
2g.240878098T>CCA2209377AGXTc.1019T>C (p.Ile340Thr)
n.797T>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.240878098T>GCA351319605AGXTc.1019T>G (p.Ile340Arg)
n.797T>G
2g.240878098T=CA1339335790AGXTc.1019T= (p.Ile340=)
n.797T=
2g.240878099A=CA1339335791AGXTc.1020A= (p.Ile340=)
n.798A=
2g.240878099A>CCA432026339AGXTc.1020A>C (p.Ile340=)
n.798A>C
2g.240878099A>GCA343786AGXTc.1020A>G (p.Ile340Met)
n.798A>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.240878099A>TCA432026341AGXTc.1020A>T (p.Ile340=)
n.798A>T
2g.240878100G>ACA351319608AGXTc.1021G>A (p.Asp341Asn)
n.799G>A
2g.240878100G>CCA351319606AGXTc.1021G>C (p.Asp341His)
n.799G>C
2g.240878100G>TCA351319607AGXTc.1021G>T (p.Asp341Tyr)
n.799G>T
2g.240878101A>CCA351319609AGXTc.1022A>C (p.Asp341Ala)
n.800A>C
2g.240878101A>GCA351319610AGXTc.1022A>G (p.Asp341Gly)
n.800A>G
2g.240878101A>TCA351319611AGXTc.1022A>T (p.Asp341Val)
n.800A>T
gnomAD v4
2g.240878102C>ACA2209378AGXTc.1023C>A (p.Asp341Glu)
n.801C>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
2g.240878102C=CA1339335792AGXTc.1023C= (p.Asp341=)
n.801C=
2g.240878102C>GCA351319612AGXTc.1023C>G (p.Asp341Glu)
n.801C>G
gnomAD v4
2g.240878102C>TCA432026351AGXTc.1023C>T (p.Asp341=)
n.801C>T
gnomAD v4
2g.240878103C>ACA351319613AGXTc.1024C>A (p.His342Asn)
n.802C>A
2g.240878103C>GCA351319614AGXTc.1024C>G (p.His342Asp)
n.802C>G
2g.240878103C>TCA351319615AGXTc.1024C>T (p.His342Tyr)
n.802C>T
2g.240878104A>CCA351319616AGXTc.1025A>C (p.His342Pro)
n.803A>C
2g.240878104A>GCA351319617AGXTc.1025A>G (p.His342Arg)
n.803A>G
2g.240878104A>TCA351319618AGXTc.1025A>T (p.His342Leu)
n.803A>T
2g.240878105C>ACA351319620AGXTc.1026C>A (p.His342Gln)
n.804C>A
2g.240878105C>GCA351319619AGXTc.1026C>G (p.His342Gln)
n.804C>G
2g.240878105C>TCA432026362AGXTc.1026C>T (p.His342=)
n.804C>T
ClinVar dbSNP
2g.240878106T>ACA351319621AGXTc.1027T>A (p.Phe343Ile)
n.805T>A
gnomAD v4
2g.240878106T>CCA351319622AGXTc.1027T>C (p.Phe343Leu)
n.805T>C
gnomAD v4
2g.240878106T>GCA351319623AGXTc.1027T>G (p.Phe343Val)
n.805T>G
gnomAD v4
2g.240878107T>ACA351319624AGXTc.1028T>A (p.Phe343Tyr)
n.806T>A
2g.240878107T>CCA351319625AGXTc.1028T>C (p.Phe343Ser)
n.806T>C
2g.240878107T>GCA351319626AGXTc.1028T>G (p.Phe343Cys)
n.806T>G
2g.240878107T=CA1339335793AGXTc.1028T= (p.Phe343=)
n.806T=
2g.240878108C>ACA351319627AGXTc.1029C>A (p.Phe343Leu)
n.807C>A
gnomAD v4
2g.240878108C=CA1339335794AGXTc.1029C= (p.Phe343=)
n.807C=
2g.240878108C>GCA351319628AGXTc.1029C>G (p.Phe343Leu)
n.807C>G
2g.240878108C>TCA2209380AGXTc.1029C>T (p.Phe343=)
n.807C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.240878108dupCA2209379AGXTc.1029dup (p.Asp344ArgfsTer3)
n.807dup
dbSNP ExAC gnomAD v2 gnomAD v4
2g.240878109G>ACA2209381AGXTc.1030G>A (p.Asp344Asn)
n.808G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.240878109G>CCA351319629AGXTc.1030G>C (p.Asp344His)
n.808G>C
2g.240878109G=CA1339335795AGXTc.1030G= (p.Asp344=)
n.808G=
2g.240878109G>TCA351319630AGXTc.1030G>T (p.Asp344Tyr)
n.808G>T
2g.240878110A>CCA351319633AGXTc.1031A>C (p.Asp344Ala)
n.809A>C
2g.240878110A>GCA351319632AGXTc.1031A>G (p.Asp344Gly)
n.809A>G
2g.240878110A>TCA351319631AGXTc.1031A>T (p.Asp344Val)
n.809A>T
2g.240878111C>ACA351319634AGXTc.1032C>A (p.Asp344Glu)
n.810C>A
2g.240878111C>GCA351319635AGXTc.1032C>G (p.Asp344Glu)
n.810C>G
2g.240878111C>TCA432026389AGXTc.1032C>T (p.Asp344=)
n.810C>T
2g.240878112A=CA1339335796AGXTc.1033A= (p.Ile345=)
n.811A=
2g.240878112A>CCA351319636AGXTc.1033A>C (p.Ile345Leu)
n.811A>C
2g.240878112A>GCA68180864AGXTc.1033A>G (p.Ile345Val)
n.811A>G
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.240878112A>TCA2209382AGXTc.1033A>T (p.Ile345Phe)
n.811A>T
dbSNP ExAC gnomAD v2 gnomAD v4
2g.240878113T>ACA351319637AGXTc.1034T>A (p.Ile345Asn)
n.812T>A
2g.240878113T>CCA351319638AGXTc.1034T>C (p.Ile345Thr)
n.812T>C
gnomAD v4
2g.240878113T>GCA351319639AGXTc.1034T>G (p.Ile345Ser)
n.812T>G
2g.240878114T>ACA432026408AGXTc.1035T>A (p.Ile345=)
n.813T>A
2g.240878114T>CCA432026410AGXTc.1035T>C (p.Ile345=)
n.813T>C
2g.240878114T>GCA351319640AGXTc.1035T>G (p.Ile345Met)
n.813T>G
2g.240878115G>ACA2209383AGXTc.1036G>A (p.Glu346Lys)
n.814G>A
dbSNP ExAC gnomAD v2 gnomAD v4
2g.240878115G>CCA351319641AGXTc.1036G>C (p.Glu346Gln)
n.814G>C
2g.240878115G=CA1339335797AGXTc.1036G= (p.Glu346=)
n.814G=
2g.240878115G>TCA351319642AGXTc.1036G>T (p.Glu346Ter)
n.814G>T
2g.240878116A>CCA351319643AGXTc.1037A>C (p.Glu346Ala)
n.815A>C
2g.240878116A>GCA351319644AGXTc.1037A>G (p.Glu346Gly)
n.815A>G
2g.240878116A>TCA351319645AGXTc.1037A>T (p.Glu346Val)
n.815A>T
2g.240878117G>ACA432026422AGXTc.1038G>A (p.Glu346=)
n.816G>A
ClinVar
2g.240878117G>CCA351319646AGXTc.1038G>C (p.Glu346Asp)
n.816G>C
2g.240878117G>TCA351319647AGXTc.1038G>T (p.Glu346Asp)
n.816G>T
2g.240878118A=CA1339335798AGXTc.1039A= (p.Ile347=)
n.817A=
2g.240878118A>CCA2209385AGXTc.1039A>C (p.Ile347Leu)
n.817A>C
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.240878118A>GCA2209384AGXTc.1039A>G (p.Ile347Val)
n.817A>G
dbSNP ExAC gnomAD v2 gnomAD v4
2g.240878118A>TCA351319648AGXTc.1039A>T (p.Ile347Phe)
n.817A>T
2g.240878119T>ACA351319649AGXTc.1040T>A (p.Ile347Asn)
n.818T>A
2g.240878119T>CCA351319650AGXTc.1040T>C (p.Ile347Thr)
n.818T>C
2g.240878119T>GCA351319651AGXTc.1040T>G (p.Ile347Ser)
n.818T>G
2g.240878120C>ACA432026433AGXTc.1041C>A (p.Ile347=)
n.819C>A
2g.240878120C=CA1339335799AGXTc.1041C= (p.Ile347=)
n.819C=
2g.240878120C>GCA351319652AGXTc.1041C>G (p.Ile347Met)
n.819C>G
dbSNP
2g.240878120C>TCA432026438AGXTc.1041C>T (p.Ile347=)
n.819C>T
ClinVar dbSNP
2g.240878121A=CA1339335800AGXTc.1042A= (p.Met348=)
n.820A=
2g.240878121A>CCA351319653AGXTc.1042A>C (p.Met348Leu)
n.820A>C
gnomAD v4
2g.240878121A>GCA2209386AGXTc.1042A>G (p.Met348Val)
n.820A>G
dbSNP ExAC gnomAD v2
2g.240878121A>TCA351319654AGXTc.1042A>T (p.Met348Leu)
n.820A>T
2g.240878122T>ACA351319655AGXTc.1043T>A (p.Met348Lys)
n.821T>A
2g.240878122T>CCA351319656AGXTc.1043T>C (p.Met348Thr)
n.821T>C
2g.240878122T>GCA351319657AGXTc.1043T>G (p.Met348Arg)
n.821T>G
2g.240878123G>ACA351319659AGXTc.1044G>A (p.Met348Ile)
n.822G>A
2g.240878123G>CCA351319660AGXTc.1044G>C (p.Met348Ile)
n.822G>C
2g.240878123G>TCA351319658AGXTc.1044G>T (p.Met348Ile)
n.822G>T
2g.240878124G>ACA275779AGXTc.1045G>A (p.Gly349Ser)
n.823G>A
ClinVar dbSNP
2g.240878124G>CCA351319661AGXTc.1045G>C (p.Gly349Arg)
n.823G>C
2g.240878124G=CA1339335801AGXTc.1045G= (p.Gly349=)
n.823G=
2g.240878124G>TCA351319662AGXTc.1045G>T (p.Gly349Cys)
n.823G>T
gnomAD v4
2g.240878124_240878125delinsAACA2580611734AGXTc.1045_1046delinsAA (p.Gly349Asn)
n.823_824delinsAA
2g.240878125G>ACA351319663AGXTc.1046G>A (p.Gly349Asp)
n.824G>A
ClinVar dbSNP
2g.240878125G>CCA351319664AGXTc.1046G>C (p.Gly349Ala)
n.824G>C
2g.240878125G=CA1339335802AGXTc.1046G= (p.Gly349=)
n.824G=
2g.240878125G>TCA351319665AGXTc.1046G>T (p.Gly349Val)
n.824G>T
2g.240878126T>ACA432026452AGXTc.1047T>A (p.Gly349=)
n.825T>A
2g.240878126T>CCA432026454AGXTc.1047T>C (p.Gly349=)
n.825T>C
2g.240878126T>GCA432026459AGXTc.1047T>G (p.Gly349=)
n.825T>G
2g.240878127G>ACA2209387AGXTc.1048G>A (p.Gly350Ser)
n.826G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.240878127G>CCA351319666AGXTc.1048G>C (p.Gly350Arg)
n.826G>C
2g.240878127G=CA1339335803AGXTc.1048G= (p.Gly350=)
n.826G=
2g.240878127G>TCA351319667AGXTc.1048G>T (p.Gly350Cys)
n.826G>T
2g.240878128G>ACA274217AGXTc.1049G>A (p.Gly350Asp)
n.827G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.240878128G>CCA351319668AGXTc.1049G>C (p.Gly350Ala)
n.827G>C
2g.240878128G=CA1339335804AGXTc.1049G= (p.Gly350=)
n.827G=
2g.240878128G>TCA2209388AGXTc.1049G>T (p.Gly350Val)
n.827G>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.240878129C>ACA432026465AGXTc.1050C>A (p.Gly350=)
n.828C>A
2g.240878129C>GCA432026467AGXTc.1050C>G (p.Gly350=)
n.828C>G
2g.240878129C>TCA432026468AGXTc.1050C>T (p.Gly350=)
n.828C>T
2g.240878130C>ACA351319670AGXTc.1051C>A (p.Leu351Ile)
n.829C>A
2g.240878130C=CA1339335805AGXTc.1051C= (p.Leu351=)
n.829C=
2g.240878130C>GCA351319671AGXTc.1051C>G (p.Leu351Val)
n.829C>G
2g.240878130C>TCA351319669AGXTc.1051C>T (p.Leu351Phe)
n.829C>T
dbSNP
2g.240878131T>ACA351319672AGXTc.1052T>A (p.Leu351His)
n.830T>A
2g.240878131T>CCA351319673AGXTc.1052T>C (p.Leu351Pro)
n.830T>C
gnomAD v4
2g.240878131T>GCA351319674AGXTc.1052T>G (p.Leu351Arg)
n.830T>G
2g.240878132T>ACA432026479AGXTc.1053T>A (p.Leu351=)
n.831T>A
2g.240878132T>CCA2209389AGXTc.1053T>C (p.Leu351=)
n.831T>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.240878132T>GCA432026483AGXTc.1053T>G (p.Leu351=)
n.831T>G
2g.240878132T=CA1339335806AGXTc.1053T= (p.Leu351=)
n.831T=
2g.240878133G>ACA351319676AGXTc.1054G>A (p.Gly352Arg)
n.832G>A
dbSNP gnomAD v3 gnomAD v4
2g.240878133G>CCA351319675AGXTc.1054G>C (p.Gly352Arg)
n.832G>C
2g.240878133G=CA1339335807AGXTc.1054G= (p.Gly352=)
n.832G=
2g.240878133G>TCA68180877AGXTc.1054G>T (p.Gly352Trp)
n.832G>T
dbSNP gnomAD v4
2g.240878134G>ACA351319677AGXTc.1055G>A (p.Gly352Glu)
n.833G>A
2g.240878134G>CCA351319678AGXTc.1055G>C (p.Gly352Ala)
n.833G>C
2g.240878134G>TCA351319679AGXTc.1055G>T (p.Gly352Val)
n.833G>T
2g.240878135G>ACA432026496AGXTc.1056G>A (p.Gly352=)
n.834G>A
ClinVar dbSNP
2g.240878135G>CCA432026497AGXTc.1056G>C (p.Gly352=)
n.834G>C
2g.240878135G=CA1339335808AGXTc.1056G= (p.Gly352=)
n.834G=
2g.240878135G>TCA432026498AGXTc.1056G>T (p.Gly352=)
n.834G>T
ClinVar dbSNP
2g.240878136C>ACA351319680AGXTc.1057C>A (p.Pro353Thr)
n.835C>A
dbSNP gnomAD v3 gnomAD v4
2g.240878136C=CA1339335809AGXTc.1057C= (p.Pro353=)
n.835C=
2g.240878136C>GCA351319681AGXTc.1057C>G (p.Pro353Ala)
n.835C>G
2g.240878136C>TCA351319682AGXTc.1057C>T (p.Pro353Ser)
n.835C>T
2g.240878137C>ACA351319684AGXTc.1058C>A (p.Pro353His)
n.836C>A
2g.240878137C=CA1339335810AGXTc.1058C= (p.Pro353=)
n.836C=
2g.240878137C>GCA351319683AGXTc.1058C>G (p.Pro353Arg)
n.836C>G
2g.240878137C>TCA68180879AGXTc.1058C>T (p.Pro353Leu)
n.836C>T
dbSNP gnomAD v3 gnomAD v4 COSMIC
2g.240878138C>ACA432026512AGXTc.1059C>A (p.Pro353=)
n.837C>A
2g.240878138C>GCA432026508AGXTc.1059C>G (p.Pro353=)
n.837C>G
2g.240878138C>TCA432026510AGXTc.1059C>T (p.Pro353=)
n.837C>T
ClinVar
2g.240878139T>ACA351319685AGXTc.1060T>A (p.Ser354Thr)
n.838T>A
2g.240878139T>CCA351319687AGXTc.1060T>C (p.Ser354Pro)
n.838T>C
2g.240878139T>GCA351319686AGXTc.1060T>G (p.Ser354Ala)
n.838T>G
2g.240878140C>ACA351319688AGXTc.1061C>A (p.Ser354Tyr)
n.839C>A
gnomAD v4
2g.240878140C=CA1339335811AGXTc.1061C= (p.Ser354=)
n.839C=
2g.240878140C>GCA351319689AGXTc.1061C>G (p.Ser354Cys)
n.839C>G
dbSNP gnomAD v2 gnomAD v4
2g.240878140C>TCA351319690AGXTc.1061C>T (p.Ser354Phe)
n.839C>T
2g.240878141C>ACA432026518AGXTc.1062C>A (p.Ser354=)
n.840C>A
2g.240878141C>GCA432026520AGXTc.1062C>G (p.Ser354=)
n.840C>G
2g.240878141C>TCA432026522AGXTc.1062C>T (p.Ser354=)
n.840C>T
2g.240878142A=CA1339335812AGXTc.1063A= (p.Thr355=)
n.841A=
2g.240878142A>CCA351319691AGXTc.1063A>C (p.Thr355Pro)
n.841A>C
dbSNP gnomAD v3 gnomAD v4
2g.240878142A>GCA351319692AGXTc.1063A>G (p.Thr355Ala)
n.841A>G
gnomAD v4
2g.240878142A>TCA351319693AGXTc.1063A>T (p.Thr355Ser)
n.841A>T
2g.240878143C>ACA2209390AGXTc.1064C>A (p.Thr355Lys)
n.842C>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.240878143C=CA1339335813AGXTc.1064C= (p.Thr355=)
n.842C=
2g.240878143C>GCA351319694AGXTc.1064C>G (p.Thr355Arg)
n.842C>G
2g.240878143C>TCA2209391AGXTc.1064C>T (p.Thr355Met)
n.842C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.240878144G>ACA2209392AGXTc.1065G>A (p.Thr355=)
n.843G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.240878144G>CCA2209393AGXTc.1065G>C (p.Thr355=)
n.843G>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.240878144G=CA1339335814AGXTc.1065G= (p.Thr355=)
n.843G=
2g.240878144G>TCA432026529AGXTc.1065G>T (p.Thr355=)
n.843G>T
2g.240878145G>ACA351319697AGXTc.1066G>A (p.Gly356Arg)
n.844G>A
dbSNP gnomAD v2 gnomAD v4
2g.240878145G>CCA351319696AGXTc.1066G>C (p.Gly356Arg)
n.844G>C
2g.240878145G=CA1339335815AGXTc.1066G= (p.Gly356=)
n.844G=
2g.240878145G>TCA351319695AGXTc.1066G>T (p.Gly356Trp)
n.844G>T

Number of alleles fetched