Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.43030447G>ACA356791880GRXCR1c.780G>A (p.Met260Ile)
c.417G>A (p.Met139Ile)
4g.43030447G>CCA356791881GRXCR1c.780G>C (p.Met260Ile)
c.417G>C (p.Met139Ile)
4g.43030447G>TCA356791882GRXCR1c.780G>T (p.Met260Ile)
c.417G>T (p.Met139Ile)
4g.43030448T>ACA356791885GRXCR1c.781T>A (p.Phe261Ile)
c.418T>A (p.Phe140Ile)
4g.43030448T>CCA356791884GRXCR1c.781T>C (p.Phe261Leu)
c.418T>C (p.Phe140Leu)
4g.43030448T>GCA356791883GRXCR1c.781T>G (p.Phe261Val)
c.418T>G (p.Phe140Val)
4g.43030449T>ACA356791886GRXCR1c.782T>A (p.Phe261Tyr)
c.419T>A (p.Phe140Tyr)
ClinVar gnomAD v4
4g.43030449T>CCA356791887GRXCR1c.782T>C (p.Phe261Ser)
c.419T>C (p.Phe140Ser)
4g.43030449T>GCA356791888GRXCR1c.782T>G (p.Phe261Cys)
c.419T>G (p.Phe140Cys)
4g.43030450T>ACA356791889GRXCR1c.783T>A (p.Phe261Leu)
c.420T>A (p.Phe140Leu)
4g.43030450T>CCA439192130GRXCR1c.783T>C (p.Phe261=)
c.420T>C (p.Phe140=)
4g.43030450T>GCA356791890GRXCR1c.783T>G (p.Phe261Leu)
c.420T>G (p.Phe140Leu)
4g.43030451C>ACA439192131GRXCR1c.784C>A (p.Arg262=)
c.421C>A (p.Arg141=)
4g.43030451C=CA1453107660GRXCR1c.784C= (p.Arg262=)
c.421C= (p.Arg141=)
4g.43030451C>GCA96319990GRXCR1c.784C>G (p.Arg262Gly)
c.421C>G (p.Arg141Gly)
dbSNP gnomAD v4
4g.43030451C>TCA2904532GRXCR1c.784C>T (p.Arg262Ter)
c.421C>T (p.Arg141Ter)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.43030452G>ACA2904533GRXCR1c.785G>A (p.Arg262Gln)
c.422G>A (p.Arg141Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.43030452G>CCA356791891GRXCR1c.785G>C (p.Arg262Pro)
c.422G>C (p.Arg141Pro)
4g.43030452G=CA1453107661GRXCR1c.785G= (p.Arg262=)
c.422G= (p.Arg141=)
4g.43030452G>TCA356791892GRXCR1c.785G>T (p.Arg262Leu)
c.422G>T (p.Arg141Leu)
ClinVar dbSNP gnomAD v3 gnomAD v4
4g.43030452_43030453delinsTTCA645531301GRXCR1c.785_786delinsTT (p.Arg262Leu)
c.422_423delinsTT (p.Arg141Leu)
COSMIC
4g.43030453A>CCA439192132GRXCR1c.786A>C (p.Arg262=)
c.423A>C (p.Arg141=)
4g.43030453A>GCA439192133GRXCR1c.786A>G (p.Arg262=)
c.423A>G (p.Arg141=)
gnomAD v4
4g.43030453A>TCA439192134GRXCR1c.786A>T (p.Arg262=)
c.423A>T (p.Arg141=)
4g.43030454A>CCA356791893GRXCR1c.787A>C (p.Asn263His)
c.424A>C (p.Asn142His)
4g.43030454A>GCA356791894GRXCR1c.787A>G (p.Asn263Asp)
c.424A>G (p.Asn142Asp)
4g.43030454A>TCA356791895GRXCR1c.787A>T (p.Asn263Tyr)
c.424A>T (p.Asn142Tyr)
4g.43030455A>CCA356791896GRXCR1c.788A>C (p.Asn263Thr)
c.425A>C (p.Asn142Thr)
4g.43030455A>GCA356791898GRXCR1c.788A>G (p.Asn263Ser)
c.425A>G (p.Asn142Ser)
4g.43030455A>TCA356791897GRXCR1c.788A>T (p.Asn263Ile)
c.425A>T (p.Asn142Ile)
gnomAD v4
4g.43030456C>ACA356791899GRXCR1c.789C>A (p.Asn263Lys)
c.426C>A (p.Asn142Lys)
4g.43030456C>GCA356791900GRXCR1c.789C>G (p.Asn263Lys)
c.426C>G (p.Asn142Lys)
gnomAD v4
4g.43030456C>TCA439192135GRXCR1c.789C>T (p.Asn263=)
c.426C>T (p.Asn142=)
4g.43030457T>ACA356791901GRXCR1c.790T>A (p.Cys264Ser)
c.427T>A (p.Cys143Ser)
4g.43030457T>CCA356791903GRXCR1c.790T>C (p.Cys264Arg)
c.427T>C (p.Cys143Arg)
gnomAD v4
4g.43030457T>GCA356791902GRXCR1c.790T>G (p.Cys264Gly)
c.427T>G (p.Cys143Gly)
gnomAD v4
4g.43030458G>ACA2904534GRXCR1c.791G>A (p.Cys264Tyr)
c.428G>A (p.Cys143Tyr)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.43030458G>CCA356791904GRXCR1c.791G>C (p.Cys264Ser)
c.428G>C (p.Cys143Ser)
4g.43030458G=CA1453107662GRXCR1c.791G= (p.Cys264=)
c.428G= (p.Cys143=)
4g.43030458G>TCA356791905GRXCR1c.791G>T (p.Cys264Phe)
c.428G>T (p.Cys143Phe)
4g.43030459C>ACA356791906GRXCR1c.792C>A (p.Cys264Ter)
c.429C>A (p.Cys143Ter)
4g.43030459C>GCA356791907GRXCR1c.792C>G (p.Cys264Trp)
c.429C>G (p.Cys143Trp)
4g.43030459C>TCA439192136GRXCR1c.792C>T (p.Cys264=)
c.429C>T (p.Cys143=)
4g.43030460T>ACA356791908GRXCR1c.793T>A (p.Phe265Ile)
c.430T>A (p.Phe144Ile)
4g.43030460T>CCA356791909GRXCR1c.793T>C (p.Phe265Leu)
c.430T>C (p.Phe144Leu)
4g.43030460T>GCA356791910GRXCR1c.793T>G (p.Phe265Val)
c.430T>G (p.Phe144Val)
4g.43030461T>ACA356791911GRXCR1c.794T>A (p.Phe265Tyr)
c.431T>A (p.Phe144Tyr)
4g.43030461T>CCA356791912GRXCR1c.794T>C (p.Phe265Ser)
c.431T>C (p.Phe144Ser)
gnomAD v4
4g.43030461T>GCA356791913GRXCR1c.794T>G (p.Phe265Cys)
c.431T>G (p.Phe144Cys)
4g.43030462C>ACA356791915GRXCR1c.795C>A (p.Phe265Leu)
c.432C>A (p.Phe144Leu)
4g.43030462C>GCA356791914GRXCR1c.795C>G (p.Phe265Leu)
c.432C>G (p.Phe144Leu)
4g.43030462C>TCA439192137GRXCR1c.795C>T (p.Phe265=)
c.432C>T (p.Phe144=)
4g.43030463A>CCA356791916GRXCR1c.796A>C (p.Thr266Pro)
c.433A>C (p.Thr145Pro)
4g.43030463A>GCA356791917GRXCR1c.796A>G (p.Thr266Ala)
c.433A>G (p.Thr145Ala)
4g.43030463A>TCA356791918GRXCR1c.796A>T (p.Thr266Ser)
c.433A>T (p.Thr145Ser)
COSMIC
4g.43030464C>ACA356791919GRXCR1c.797C>A (p.Thr266Lys)
c.434C>A (p.Thr145Lys)
4g.43030464C=CA1453107663GRXCR1c.797C= (p.Thr266=)
c.434C= (p.Thr145=)
4g.43030464C>GCA356791920GRXCR1c.797C>G (p.Thr266Arg)
c.434C>G (p.Thr145Arg)
gnomAD v4
4g.43030464C>TCA356791921GRXCR1c.797C>T (p.Thr266Ile)
c.434C>T (p.Thr145Ile)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.43030465A>CCA439192138GRXCR1c.798A>C (p.Thr266=)
c.435A>C (p.Thr145=)
4g.43030465A>GCA439192139GRXCR1c.798A>G (p.Thr266=)
c.435A>G (p.Thr145=)
4g.43030465A>TCA439192140GRXCR1c.798A>T (p.Thr266=)
c.435A>T (p.Thr145=)
4g.43030466G>ACA356791922GRXCR1c.799G>A (p.Asp267Asn)
c.436G>A (p.Asp146Asn)
COSMIC
4g.43030466G>CCA356791923GRXCR1c.799G>C (p.Asp267His)
c.436G>C (p.Asp146His)
4g.43030466G>TCA356791924GRXCR1c.799G>T (p.Asp267Tyr)
c.436G>T (p.Asp146Tyr)
4g.43030467A>CCA356791925GRXCR1c.800A>C (p.Asp267Ala)
c.437A>C (p.Asp146Ala)
4g.43030467A>GCA356791926GRXCR1c.800A>G (p.Asp267Gly)
c.437A>G (p.Asp146Gly)
gnomAD v4
4g.43030467A>TCA356791927GRXCR1c.800A>T (p.Asp267Val)
c.437A>T (p.Asp146Val)
4g.43030468C>ACA356791929GRXCR1c.801C>A (p.Asp267Glu)
c.438C>A (p.Asp146Glu)
4g.43030468C=CA1453107664GRXCR1c.801C= (p.Asp267=)
c.438C= (p.Asp146=)
4g.43030468C>GCA356791928GRXCR1c.801C>G (p.Asp267Glu)
c.438C>G (p.Asp146Glu)
dbSNP gnomAD v3 gnomAD v4
4g.43030468C>TCA439192141GRXCR1c.801C>T (p.Asp267=)
c.438C>T (p.Asp146=)
4g.43030470_43030471delCA2578077019GRXCR1c.803_804del (p.Ser268PhefsTer11)
c.440_441del (p.Ser147PhefsTer11)
4g.43030469T>ACA356791930GRXCR1c.802T>A (p.Ser268Thr)
c.439T>A (p.Ser147Thr)
4g.43030469T>CCA356791931GRXCR1c.802T>C (p.Ser268Pro)
c.439T>C (p.Ser147Pro)
COSMIC
4g.43030469T>GCA356791932GRXCR1c.802T>G (p.Ser268Ala)
c.439T>G (p.Ser147Ala)
4g.43030470C>ACA356791933GRXCR1c.803C>A (p.Ser268Tyr)
c.440C>A (p.Ser147Tyr)
ClinVar dbSNP
4g.43030470C>GCA356791934GRXCR1c.803C>G (p.Ser268Cys)
c.440C>G (p.Ser147Cys)
gnomAD v4
4g.43030470C>TCA356791935GRXCR1c.803C>T (p.Ser268Phe)
c.440C>T (p.Ser147Phe)
gnomAD v4
4g.43030471T>ACA439192144GRXCR1c.804T>A (p.Ser268=)
c.441T>A (p.Ser147=)
4g.43030471T>CCA439192143GRXCR1c.804T>C (p.Ser268=)
c.441T>C (p.Ser147=)
4g.43030471T>GCA439192142GRXCR1c.804T>G (p.Ser268=)
c.441T>G (p.Ser147=)
gnomAD v4
4g.43030472T>ACA356791938GRXCR1c.805T>A (p.Phe269Ile)
c.442T>A (p.Phe148Ile)
4g.43030472T>CCA356791936GRXCR1c.805T>C (p.Phe269Leu)
c.442T>C (p.Phe148Leu)
4g.43030472T>GCA356791937GRXCR1c.805T>G (p.Phe269Val)
c.442T>G (p.Phe148Val)
4g.43030473T>ACA356791939GRXCR1c.806T>A (p.Phe269Tyr)
c.443T>A (p.Phe148Tyr)
4g.43030473T>CCA356791940GRXCR1c.806T>C (p.Phe269Ser)
c.443T>C (p.Phe148Ser)
4g.43030473T>GCA356791941GRXCR1c.806T>G (p.Phe269Cys)
c.443T>G (p.Phe148Cys)
4g.43030474C>ACA356791942GRXCR1c.807C>A (p.Phe269Leu)
c.444C>A (p.Phe148Leu)
4g.43030474C=CA1453107665GRXCR1c.807C= (p.Phe269=)
c.444C= (p.Phe148=)
4g.43030474C>GCA2904535GRXCR1c.807C>G (p.Phe269Leu)
c.444C>G (p.Phe148Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.43030474C>TCA439192145GRXCR1c.807C>T (p.Phe269=)
c.444C>T (p.Phe148=)
4g.43030475A=CA1453107666GRXCR1c.808A= (p.Lys270=)
c.445A= (p.Lys149=)
4g.43030475A>CCA356791943GRXCR1c.808A>C (p.Lys270Gln)
c.445A>C (p.Lys149Gln)
4g.43030475A>GCA356791945GRXCR1c.808A>G (p.Lys270Glu)
c.445A>G (p.Lys149Glu)
dbSNP gnomAD v2 gnomAD v4
4g.43030475A>TCA356791944GRXCR1c.808A>T (p.Lys270Ter)
c.445A>T (p.Lys149Ter)
4g.43030476A=CA1453107667GRXCR1c.809A= (p.Lys270=)
c.446A= (p.Lys149=)
4g.43030476A>CCA356791946GRXCR1c.809A>C (p.Lys270Thr)
c.446A>C (p.Lys149Thr)
4g.43030476A>GCA356791947GRXCR1c.809A>G (p.Lys270Arg)
c.446A>G (p.Lys149Arg)
4g.43030476A>TCA356791948GRXCR1c.809A>T (p.Lys270Ile)
c.446A>T (p.Lys149Ile)
dbSNP
4g.43030477A>CCA356791949GRXCR1c.810A>C (p.Lys270Asn)
c.447A>C (p.Lys149Asn)
4g.43030477A>GCA439192146GRXCR1c.810A>G (p.Lys270=)
c.447A>G (p.Lys149=)
4g.43030477A>TCA356791950GRXCR1c.810A>T (p.Lys270Asn)
c.447A>T (p.Lys149Asn)
4g.43030478G>ACA356791951GRXCR1c.811G>A (p.Ala271Thr)
c.448G>A (p.Ala150Thr)
gnomAD v4
4g.43030478G>CCA356791952GRXCR1c.811G>C (p.Ala271Pro)
c.448G>C (p.Ala150Pro)
4g.43030478G>TCA356791953GRXCR1c.811G>T (p.Ala271Ser)
c.448G>T (p.Ala150Ser)
gnomAD v4
4g.43030479C>ACA356791954GRXCR1c.812C>A (p.Ala271Asp)
c.449C>A (p.Ala150Asp)
4g.43030479C>GCA356791955GRXCR1c.812C>G (p.Ala271Gly)
c.449C>G (p.Ala150Gly)
4g.43030479C>TCA356791956GRXCR1c.812C>T (p.Ala271Val)
c.449C>T (p.Ala150Val)
gnomAD v4
4g.43030480C>ACA176273GRXCR1c.813C>A (p.Ala271=)
c.450C>A (p.Ala150=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.43030480C=CA1453107668GRXCR1c.813C= (p.Ala271=)
c.450C= (p.Ala150=)
4g.43030480C>GCA439192147GRXCR1c.813C>G (p.Ala271=)
c.450C>G (p.Ala150=)
4g.43030480C>TCA439192148GRXCR1c.813C>T (p.Ala271=)
c.450C>T (p.Ala150=)
4g.43030481C>ACA356791958GRXCR1c.814C>A (p.Leu272Met)
c.451C>A (p.Leu151Met)
4g.43030481C=CA1453107669GRXCR1c.814C= (p.Leu272=)
c.451C= (p.Leu151=)
4g.43030481C>GCA356791957GRXCR1c.814C>G (p.Leu272Val)
c.451C>G (p.Leu151Val)
dbSNP
4g.43030481C>TCA439192149GRXCR1c.814C>T (p.Leu272=)
c.451C>T (p.Leu151=)
gnomAD v4
4g.43030482T>ACA356791959GRXCR1c.815T>A (p.Leu272Gln)
c.452T>A (p.Leu151Gln)
4g.43030482T>CCA356791961GRXCR1c.815T>C (p.Leu272Pro)
c.452T>C (p.Leu151Pro)
gnomAD v4
4g.43030482T>GCA356791960GRXCR1c.815T>G (p.Leu272Arg)
c.452T>G (p.Leu151Arg)
4g.43030486_43030504delCA2670496247GRXCR1c.819_837del (p.Cys274MetfsTer24)
c.456_474del (p.Cys153MetfsTer24)
gnomAD v4
4g.43030483G>ACA439192150GRXCR1c.816G>A (p.Leu272=)
c.453G>A (p.Leu151=)
dbSNP gnomAD v4
4g.43030483G>CCA439192151GRXCR1c.816G>C (p.Leu272=)
c.453G>C (p.Leu151=)
4g.43030483G=CA1453107670GRXCR1c.816G= (p.Leu272=)
c.453G= (p.Leu151=)
4g.43030483G>TCA439192152GRXCR1c.816G>T (p.Leu272=)
c.453G>T (p.Leu151=)
4g.43030484A>CCA356791962GRXCR1c.817A>C (p.Lys273Gln)
c.454A>C (p.Lys152Gln)
4g.43030484A>GCA356791963GRXCR1c.817A>G (p.Lys273Glu)
c.454A>G (p.Lys152Glu)
4g.43030484A>TCA356791964GRXCR1c.817A>T (p.Lys273Ter)
c.454A>T (p.Lys152Ter)
4g.43030485A>CCA356791965GRXCR1c.818A>C (p.Lys273Thr)
c.455A>C (p.Lys152Thr)
4g.43030485A>GCA356791966GRXCR1c.818A>G (p.Lys273Arg)
c.455A>G (p.Lys152Arg)
4g.43030485A>TCA356791967GRXCR1c.818A>T (p.Lys273Met)
c.455A>T (p.Lys152Met)
4g.43030486G>ACA439192153GRXCR1c.819G>A (p.Lys273=)
c.456G>A (p.Lys152=)
dbSNP
4g.43030486G>CCA356791968GRXCR1c.819G>C (p.Lys273Asn)
c.456G>C (p.Lys152Asn)
4g.43030486G=CA1453107671GRXCR1c.819G= (p.Lys273=)
c.456G= (p.Lys152=)
4g.43030486G>TCA356791969GRXCR1c.819G>T (p.Lys273Asn)
c.456G>T (p.Lys152Asn)
4g.43030487T>ACA356791970GRXCR1c.820T>A (p.Cys274Ser)
c.457T>A (p.Cys153Ser)
4g.43030487T>CCA356791971GRXCR1c.820T>C (p.Cys274Arg)
c.457T>C (p.Cys153Arg)
dbSNP
4g.43030487T>GCA356791972GRXCR1c.820T>G (p.Cys274Gly)
c.457T>G (p.Cys153Gly)
4g.43030487T=CA1453107672GRXCR1c.820T= (p.Cys274=)
c.457T= (p.Cys153=)
4g.43030488G>ACA356791975GRXCR1c.821G>A (p.Cys274Tyr)
c.458G>A (p.Cys153Tyr)
gnomAD v4
4g.43030488G>CCA356791974GRXCR1c.821G>C (p.Cys274Ser)
c.458G>C (p.Cys153Ser)
4g.43030488G>TCA356791973GRXCR1c.821G>T (p.Cys274Phe)
c.458G>T (p.Cys153Phe)
COSMIC
4g.43030489T>ACA356791976GRXCR1c.822T>A (p.Cys274Ter)
c.459T>A (p.Cys153Ter)
gnomAD v4
4g.43030489T>CCA439192154GRXCR1c.822T>C (p.Cys274=)
c.459T>C (p.Cys153=)
ClinVar dbSNP gnomAD v2 gnomAD v4
4g.43030489T>GCA356791977GRXCR1c.822T>G (p.Cys274Trp)
c.459T>G (p.Cys153Trp)
4g.43030489T=CA1453107673GRXCR1c.822T= (p.Cys274=)
c.459T= (p.Cys153=)
4g.43030490A=CA1453107674GRXCR1c.823A= (p.Thr275=)
c.460A= (p.Thr154=)
4g.43030490A>CCA2904536GRXCR1c.823A>C (p.Thr275Pro)
c.460A>C (p.Thr154Pro)
dbSNP ExAC gnomAD v2
4g.43030490A>GCA356791978GRXCR1c.823A>G (p.Thr275Ala)
c.460A>G (p.Thr154Ala)
4g.43030490A>TCA356791979GRXCR1c.823A>T (p.Thr275Ser)
c.460A>T (p.Thr154Ser)
4g.43030491C>ACA2904537GRXCR1c.824C>A (p.Thr275Lys)
c.461C>A (p.Thr154Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.43030491C=CA1453107675GRXCR1c.824C= (p.Thr275=)
c.461C= (p.Thr154=)
4g.43030491C>GCA356791980GRXCR1c.824C>G (p.Thr275Arg)
c.461C>G (p.Thr154Arg)
4g.43030491C>TCA2904538GRXCR1c.824C>T (p.Thr275Met)
c.461C>T (p.Thr154Met)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.43030492G>ACA2904539GRXCR1c.825G>A (p.Thr275=)
c.462G>A (p.Thr154=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.43030492G>CCA439192156GRXCR1c.825G>C (p.Thr275=)
c.462G>C (p.Thr154=)
4g.43030492G=CA1453107676GRXCR1c.825G= (p.Thr275=)
c.462G= (p.Thr154=)
4g.43030492G>TCA439192155GRXCR1c.825G>T (p.Thr275=)
c.462G>T (p.Thr154=)
4g.43030493G>ACA96319991GRXCR1c.826G>A (p.Ala276Thr)
c.463G>A (p.Ala155Thr)
dbSNP gnomAD v3 gnomAD v4
4g.43030493G>CCA356791981GRXCR1c.826G>C (p.Ala276Pro)
c.463G>C (p.Ala155Pro)
4g.43030493G=CA1453107677GRXCR1c.826G= (p.Ala276=)
c.463G= (p.Ala155=)
4g.43030493G>TCA356791982GRXCR1c.826G>T (p.Ala276Ser)
c.463G>T (p.Ala155Ser)
COSMIC
4g.43030494C>ACA356791985GRXCR1c.827C>A (p.Ala276Asp)
c.464C>A (p.Ala155Asp)
4g.43030494C>GCA356791984GRXCR1c.827C>G (p.Ala276Gly)
c.464C>G (p.Ala155Gly)
4g.43030494C>TCA356791983GRXCR1c.827C>T (p.Ala276Val)
c.464C>T (p.Ala155Val)
4g.43030495T>ACA2904540GRXCR1c.828T>A (p.Ala276=)
c.465T>A (p.Ala155=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.43030495T>CCA439192157GRXCR1c.828T>C (p.Ala276=)
c.465T>C (p.Ala155=)
4g.43030495T>GCA439192158GRXCR1c.828T>G (p.Ala276=)
c.465T>G (p.Ala155=)
4g.43030495T=CA1453107678GRXCR1c.828T= (p.Ala276=)
c.465T= (p.Ala155=)
4g.43030496T>ACA356791986GRXCR1c.829T>A (p.Cys277Ser)
c.466T>A (p.Cys156Ser)
gnomAD v4
4g.43030496T>CCA356791987GRXCR1c.829T>C (p.Cys277Arg)
c.466T>C (p.Cys156Arg)
dbSNP COSMIC
4g.43030496T>GCA356791988GRXCR1c.829T>G (p.Cys277Gly)
c.466T>G (p.Cys156Gly)
4g.43030496T=CA1453107679GRXCR1c.829T= (p.Cys277=)
c.466T= (p.Cys156=)
4g.43030497G>ACA356791989GRXCR1c.830G>A (p.Cys277Tyr)
c.467G>A (p.Cys156Tyr)
4g.43030497G>CCA356791990GRXCR1c.830G>C (p.Cys277Ser)
c.467G>C (p.Cys156Ser)
4g.43030497G>TCA356791991GRXCR1c.830G>T (p.Cys277Phe)
c.467G>T (p.Cys156Phe)
4g.43030498C>ACA356791992GRXCR1c.831C>A (p.Cys277Ter)
c.468C>A (p.Cys156Ter)
4g.43030498C>GCA356791993GRXCR1c.831C>G (p.Cys277Trp)
c.468C>G (p.Cys156Trp)
4g.43030498C>TCA439192159GRXCR1c.831C>T (p.Cys277=)
c.468C>T (p.Cys156=)
4g.43030499A>CCA356791994GRXCR1c.832A>C (p.Asn278His)
c.469A>C (p.Asn157His)
4g.43030499A>GCA356791995GRXCR1c.832A>G (p.Asn278Asp)
c.469A>G (p.Asn157Asp)
4g.43030499A>TCA356791996GRXCR1c.832A>T (p.Asn278Tyr)
c.469A>T (p.Asn157Tyr)
4g.43030500A>CCA356791998GRXCR1c.833A>C (p.Asn278Thr)
c.470A>C (p.Asn157Thr)
4g.43030500A>GCA356791999GRXCR1c.833A>G (p.Asn278Ser)
c.470A>G (p.Asn157Ser)
4g.43030500A>TCA356791997GRXCR1c.833A>T (p.Asn278Ile)
c.470A>T (p.Asn157Ile)
4g.43030501T>ACA356792000GRXCR1c.834T>A (p.Asn278Lys)
c.471T>A (p.Asn157Lys)
4g.43030501T>CCA439192160GRXCR1c.834T>C (p.Asn278=)
c.471T>C (p.Asn157=)
dbSNP gnomAD v2 gnomAD v4
4g.43030501T>GCA356792001GRXCR1c.834T>G (p.Asn278Lys)
c.471T>G (p.Asn157Lys)
4g.43030501T=CA1453107680GRXCR1c.834T= (p.Asn278=)
c.471T= (p.Asn157=)
4g.43030502G>ACA356792002GRXCR1c.835G>A (p.Glu279Lys)
c.472G>A (p.Glu158Lys)
gnomAD v4
4g.43030502G>CCA356792003GRXCR1c.835G>C (p.Glu279Gln)
c.472G>C (p.Glu158Gln)
4g.43030502G>TCA356792004GRXCR1c.835G>T (p.Glu279Ter)
c.472G>T (p.Glu158Ter)
COSMIC
4g.43030503A>CCA356792007GRXCR1c.836A>C (p.Glu279Ala)
c.473A>C (p.Glu158Ala)
4g.43030503A>GCA356792005GRXCR1c.836A>G (p.Glu279Gly)
c.473A>G (p.Glu158Gly)
4g.43030503A>TCA356792006GRXCR1c.836A>T (p.Glu279Val)
c.473A>T (p.Glu158Val)
4g.43030506delCA2578077020GRXCR1c.839del (p.Asn280MetfsTer24)
c.476del (p.Asn159MetfsTer24)
4g.43030504A>CCA356792008GRXCR1c.837A>C (p.Glu279Asp)
c.474A>C (p.Glu158Asp)
4g.43030504A>GCA439192161GRXCR1c.837A>G (p.Glu279=)
c.474A>G (p.Glu158=)
4g.43030504A>TCA356792009GRXCR1c.837A>T (p.Glu279Asp)
c.474A>T (p.Glu158Asp)
4g.43030505A>CCA356792010GRXCR1c.838A>C (p.Asn280His)
c.475A>C (p.Asn159His)
4g.43030505A>GCA356792011GRXCR1c.838A>G (p.Asn280Asp)
c.475A>G (p.Asn159Asp)
4g.43030505A>TCA356792012GRXCR1c.838A>T (p.Asn280Tyr)
c.475A>T (p.Asn159Tyr)
4g.43030506A>CCA356792013GRXCR1c.839A>C (p.Asn280Thr)
c.476A>C (p.Asn159Thr)
4g.43030506A>GCA356792015GRXCR1c.839A>G (p.Asn280Ser)
c.476A>G (p.Asn159Ser)
4g.43030506A>TCA356792014GRXCR1c.839A>T (p.Asn280Ile)
c.476A>T (p.Asn159Ile)
4g.43030507T>ACA356792016GRXCR1c.840T>A (p.Asn280Lys)
c.477T>A (p.Asn159Lys)
gnomAD v4
4g.43030507T>CCA439192162GRXCR1c.840T>C (p.Asn280=)
c.477T>C (p.Asn159=)
4g.43030507T>GCA356792017GRXCR1c.840T>G (p.Asn280Lys)
c.477T>G (p.Asn159Lys)
4g.43030508G>ACA356792018GRXCR1c.841G>A (p.Gly281Ser)
c.478G>A (p.Gly160Ser)
4g.43030508G>CCA2904541GRXCR1c.841G>C (p.Gly281Arg)
c.478G>C (p.Gly160Arg)
dbSNP ExAC
4g.43030508G=CA1453107681GRXCR1c.841G= (p.Gly281=)
c.478G= (p.Gly160=)
4g.43030508G>TCA356792019GRXCR1c.841G>T (p.Gly281Cys)
c.478G>T (p.Gly160Cys)
4g.43030509G>ACA356792020GRXCR1c.842G>A (p.Gly281Asp)
c.479G>A (p.Gly160Asp)
gnomAD v4
4g.43030509G>CCA356792021GRXCR1c.842G>C (p.Gly281Ala)
c.479G>C (p.Gly160Ala)
4g.43030509G>TCA356792022GRXCR1c.842G>T (p.Gly281Val)
c.479G>T (p.Gly160Val)
4g.43030510T>ACA439192163GRXCR1c.843T>A (p.Gly281=)
c.480T>A (p.Gly160=)
4g.43030510T>CCA439192164GRXCR1c.843T>C (p.Gly281=)
c.480T>C (p.Gly160=)
4g.43030510T>GCA439192165GRXCR1c.843T>G (p.Gly281=)
c.480T>G (p.Gly160=)
dbSNP
4g.43030510T=CA1453107682GRXCR1c.843T= (p.Gly281=)
c.480T= (p.Gly160=)
4g.43030511C>ACA356792023GRXCR1c.844C>A (p.Leu282Ile)
c.481C>A (p.Leu161Ile)
4g.43030511C=CA1453107683GRXCR1c.844C= (p.Leu282=)
c.481C= (p.Leu161=)
4g.43030511C>GCA356792024GRXCR1c.844C>G (p.Leu282Val)
c.481C>G (p.Leu161Val)
4g.43030511C>TCA356792025GRXCR1c.844C>T (p.Leu282Phe)
c.481C>T (p.Leu161Phe)
dbSNP gnomAD v2 gnomAD v4
4g.43030512T>ACA356792026GRXCR1c.845T>A (p.Leu282His)
c.482T>A (p.Leu161His)
4g.43030512T>CCA356792027GRXCR1c.845T>C (p.Leu282Pro)
c.482T>C (p.Leu161Pro)
4g.43030512T>GCA356792028GRXCR1c.845T>G (p.Leu282Arg)
c.482T>G (p.Leu161Arg)
4g.43030513T>ACA439192166GRXCR1c.846T>A (p.Leu282=)
c.483T>A (p.Leu161=)
4g.43030513T>CCA439192168GRXCR1c.846T>C (p.Leu282=)
c.483T>C (p.Leu161=)
4g.43030513T>GCA439192167GRXCR1c.846T>G (p.Leu282=)
c.483T>G (p.Leu161=)
4g.43030514C>ACA356792029GRXCR1c.847C>A (p.Gln283Lys)
c.484C>A (p.Gln162Lys)
COSMIC
4g.43030514C>GCA356792030GRXCR1c.847C>G (p.Gln283Glu)
c.484C>G (p.Gln162Glu)
4g.43030514C>TCA356792031GRXCR1c.847C>T (p.Gln283Ter)
c.484C>T (p.Gln162Ter)
4g.43030515A=CA1453107684GRXCR1c.848A= (p.Gln283=)
c.485A= (p.Gln162=)
4g.43030515A>CCA356792034GRXCR1c.848A>C (p.Gln283Pro)
c.485A>C (p.Gln162Pro)
4g.43030515A>GCA356792032GRXCR1c.848A>G (p.Gln283Arg)
c.485A>G (p.Gln162Arg)
dbSNP gnomAD v4
4g.43030515A>TCA356792033GRXCR1c.848A>T (p.Gln283Leu)
c.485A>T (p.Gln162Leu)
gnomAD v4
4g.43030516G>ACA439192169GRXCR1c.849G>A (p.Gln283=)
c.486G>A (p.Gln162=)
gnomAD v4
4g.43030516G>CCA356792035GRXCR1c.849G>C (p.Gln283His)
c.486G>C (p.Gln162His)
gnomAD v4
4g.43030516G>TCA356792036GRXCR1c.849G>T (p.Gln283His)
c.486G>T (p.Gln162His)
4g.43030517C>ACA356792037GRXCR1c.850C>A (p.Arg284Ser)
c.487C>A (p.Arg163Ser)
4g.43030517C=CA1453107685GRXCR1c.850C= (p.Arg284=)
c.487C= (p.Arg163=)
4g.43030517C>GCA356792038GRXCR1c.850C>G (p.Arg284Gly)
c.487C>G (p.Arg163Gly)
4g.43030517C>TCA2904542GRXCR1c.850C>T (p.Arg284Cys)
c.487C>T (p.Arg163Cys)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.43030518G>ACA2904543GRXCR1c.851G>A (p.Arg284His)
c.488G>A (p.Arg163His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.43030518G>CCA356792039GRXCR1c.851G>C (p.Arg284Pro)
c.488G>C (p.Arg163Pro)
4g.43030518G=CA1453107686GRXCR1c.851G= (p.Arg284=)
c.488G= (p.Arg163=)
4g.43030518G>TCA356792040GRXCR1c.851G>T (p.Arg284Leu)
c.488G>T (p.Arg163Leu)
dbSNP gnomAD v2 gnomAD v4
4g.43030519T>ACA439192170GRXCR1c.852T>A (p.Arg284=)
c.489T>A (p.Arg163=)
4g.43030519T>CCA439192171GRXCR1c.852T>C (p.Arg284=)
c.489T>C (p.Arg163=)
dbSNP gnomAD v2
4g.43030519T>GCA439192172GRXCR1c.852T>G (p.Arg284=)
c.489T>G (p.Arg163=)
4g.43030519T=CA1453107687GRXCR1c.852T= (p.Arg284=)
c.489T= (p.Arg163=)
4g.43030520T>ACA356792041GRXCR1c.853T>A (p.Cys285Ser)
c.490T>A (p.Cys164Ser)
4g.43030520T>CCA356792042GRXCR1c.853T>C (p.Cys285Arg)
c.490T>C (p.Cys164Arg)
4g.43030520T>GCA356792043GRXCR1c.853T>G (p.Cys285Gly)
c.490T>G (p.Cys164Gly)
4g.43030521G>ACA356792046GRXCR1c.854G>A (p.Cys285Tyr)
c.491G>A (p.Cys164Tyr)
4g.43030521G>CCA356792045GRXCR1c.854G>C (p.Cys285Ser)
c.491G>C (p.Cys164Ser)
4g.43030521G=CA1453107688GRXCR1c.854G= (p.Cys285=)
c.491G= (p.Cys164=)
4g.43030521G>TCA356792044GRXCR1c.854G>T (p.Cys285Phe)
c.491G>T (p.Cys164Phe)
dbSNP
4g.43030522T>ACA356792048GRXCR1c.855T>A (p.Cys285Ter)
c.492T>A (p.Cys164Ter)
4g.43030522T>CCA439192173GRXCR1c.855T>C (p.Cys285=)
c.492T>C (p.Cys164=)
gnomAD v4
4g.43030522T>GCA356792047GRXCR1c.855T>G (p.Cys285Trp)
c.492T>G (p.Cys164Trp)
4g.43030523A=CA1453107689GRXCR1c.856A= (p.Lys286=)
c.493A= (p.Lys165=)
4g.43030523A>CCA356792049GRXCR1c.856A>C (p.Lys286Gln)
c.493A>C (p.Lys165Gln)
4g.43030523A>GCA356792050GRXCR1c.856A>G (p.Lys286Glu)
c.493A>G (p.Lys165Glu)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.43030523A>TCA356792051GRXCR1c.856A>T (p.Lys286Ter)
c.493A>T (p.Lys165Ter)
4g.43030524A=CA1453107690GRXCR1c.857A= (p.Lys286=)
c.494A= (p.Lys165=)
4g.43030524A>CCA2904544GRXCR1c.857A>C (p.Lys286Thr)
c.494A>C (p.Lys165Thr)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.43030524A>GCA356792052GRXCR1c.857A>G (p.Lys286Arg)
c.494A>G (p.Lys165Arg)
4g.43030524A>TCA356792053GRXCR1c.857A>T (p.Lys286Met)
c.494A>T (p.Lys165Met)
4g.43030525G>ACA439192174GRXCR1c.858G>A (p.Lys286=)
c.495G>A (p.Lys165=)
COSMIC
4g.43030525G>CCA356792054GRXCR1c.858G>C (p.Lys286Asn)
c.495G>C (p.Lys165Asn)
4g.43030525G=CA1453107691GRXCR1c.858G= (p.Lys286=)
c.495G= (p.Lys165=)
4g.43030525G>TCA10621072GRXCR1c.858G>T (p.Lys286Asn)
c.495G>T (p.Lys165Asn)
ClinVar dbSNP
4g.43030526A>CCA356792055GRXCR1c.859A>C (p.Asn287His)
c.496A>C (p.Asn166His)
4g.43030526A>GCA356792056GRXCR1c.859A>G (p.Asn287Asp)
c.496A>G (p.Asn166Asp)
4g.43030526A>TCA356792057GRXCR1c.859A>T (p.Asn287Tyr)
c.496A>T (p.Asn166Tyr)
4g.43030527A>CCA356792060GRXCR1c.860A>C (p.Asn287Thr)
c.497A>C (p.Asn166Thr)
COSMIC
4g.43030527A>GCA356792059GRXCR1c.860A>G (p.Asn287Ser)
c.497A>G (p.Asn166Ser)
gnomAD v4
4g.43030527A>TCA356792058GRXCR1c.860A>T (p.Asn287Ile)
c.497A>T (p.Asn166Ile)
4g.43030528C>ACA356792061GRXCR1c.861C>A (p.Asn287Lys)
c.498C>A (p.Asn166Lys)
4g.43030528C>GCA356792062GRXCR1c.861C>G (p.Asn287Lys)
c.498C>G (p.Asn166Lys)
4g.43030528C>TCA439192175GRXCR1c.861C>T (p.Asn287=)
c.498C>T (p.Asn166=)
gnomAD v4
4g.43030529T>ACA356792063GRXCR1c.862T>A (p.Cys288Ser)
c.499T>A (p.Cys167Ser)
4g.43030529T>CCA356792064GRXCR1c.862T>C (p.Cys288Arg)
c.499T>C (p.Cys167Arg)
4g.43030529T>GCA356792065GRXCR1c.862T>G (p.Cys288Gly)
c.499T>G (p.Cys167Gly)
4g.43030530G>ACA2904545GRXCR1c.863G>A (p.Cys288Tyr)
c.500G>A (p.Cys167Tyr)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.43030530G>CCA356792066GRXCR1c.863G>C (p.Cys288Ser)
c.500G>C (p.Cys167Ser)
4g.43030530G=CA1453107692GRXCR1c.863G= (p.Cys288=)
c.500G= (p.Cys167=)
4g.43030530G>TCA356792067GRXCR1c.863G>T (p.Cys288Phe)
c.500G>T (p.Cys167Phe)
4g.43030531T>ACA356792068GRXCR1c.864T>A (p.Cys288Ter)
c.501T>A (p.Cys167Ter)
4g.43030531T>CCA439192176GRXCR1c.864T>C (p.Cys288=)
c.501T>C (p.Cys167=)
gnomAD v4
4g.43030531T>GCA356792069GRXCR1c.864T>G (p.Cys288Trp)
c.501T>G (p.Cys167Trp)
4g.43030532G>ACA356792070GRXCR1c.865G>A (p.Ala289Thr)
c.502G>A (p.Ala168Thr)
4g.43030532G>CCA356792071GRXCR1c.865G>C (p.Ala289Pro)
c.502G>C (p.Ala168Pro)
4g.43030532G>TCA356792072GRXCR1c.865G>T (p.Ala289Ser)
c.502G>T (p.Ala168Ser)
4g.43030533C>ACA356792074GRXCR1c.866C>A (p.Ala289Asp)
c.503C>A (p.Ala168Asp)
ClinVar gnomAD v4
4g.43030533C=CA1453107693GRXCR1c.866C= (p.Ala289=)
c.503C= (p.Ala168=)
4g.43030533C>GCA356792075GRXCR1c.866C>G (p.Ala289Gly)
c.503C>G (p.Ala168Gly)
4g.43030533C>TCA356792073GRXCR1c.866C>T (p.Ala289Val)
c.503C>T (p.Ala168Val)
dbSNP
4g.43030534T>ACA439192177GRXCR1c.867T>A (p.Ala289=)
c.504T>A (p.Ala168=)
4g.43030534T>CCA439192178GRXCR1c.867T>C (p.Ala289=)
c.504T>C (p.Ala168=)
4g.43030534T>GCA439192179GRXCR1c.867T>G (p.Ala289=)
c.504T>G (p.Ala168=)
4g.43030535G>ACA356792076GRXCR1c.868G>A (p.Gly290Ser)
c.505G>A (p.Gly169Ser)
dbSNP gnomAD v3 gnomAD v4
4g.43030535G>CCA2904546GRXCR1c.868G>C (p.Gly290Arg)
c.505G>C (p.Gly169Arg)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.43030535G=CA1453107694GRXCR1c.868G= (p.Gly290=)
c.505G= (p.Gly169=)
4g.43030535G>TCA356792077GRXCR1c.868G>T (p.Gly290Cys)
c.505G>T (p.Gly169Cys)
4g.43030536G>ACA356792078GRXCR1c.869G>A (p.Gly290Asp)
c.506G>A (p.Gly169Asp)
COSMIC
4g.43030536G>CCA356792079GRXCR1c.869G>C (p.Gly290Ala)
c.506G>C (p.Gly169Ala)
4g.43030536G=CA1453107695GRXCR1c.869G= (p.Gly290=)
c.506G= (p.Gly169=)
4g.43030536G>TCA356792080GRXCR1c.869G>T (p.Gly290Val)
c.506G>T (p.Gly169Val)
dbSNP
4g.43030537T>ACA439192180GRXCR1c.870T>A (p.Gly290=)
c.507T>A (p.Gly169=)
4g.43030537T>CCA439192181GRXCR1c.870T>C (p.Gly290=)
c.507T>C (p.Gly169=)
4g.43030537T>GCA439192182GRXCR1c.870T>G (p.Gly290=)
c.507T>G (p.Gly169=)
gnomAD v4
4g.43030538T>ACA356792081GRXCR1c.871T>A (p.Ter291Lys)
c.508T>A (p.Ter170Lys)
4g.43030538T>CCA356792082GRXCR1c.871T>C (p.Ter291Gln)
c.508T>C (p.Ter170Gln)
dbSNP
4g.43030538T>GCA356792083GRXCR1c.871T>G (p.Ter291Glu)
c.508T>G (p.Ter170Glu)
gnomAD v4
4g.43030538T=CA1453107696GRXCR1c.871T= (p.Ter291=)
c.508T= (p.Ter170=)
4g.43030539A>CCA356792084GRXCR1c.872A>C (p.Ter291Ser)
c.509A>C (p.Ter170Ser)
4g.43030539A>GCA439192183GRXCR1c.872A>G (p.Ter291=)
c.509A>G (p.Ter170=)
4g.43030539A>TCA356792085GRXCR1c.872A>T (p.Ter291Leu)
c.509A>T (p.Ter170Leu)
4g.43030540A>CCA356792086GRXCR1c.873A>C (p.Ter291Tyr)
c.510A>C (p.Ter170Tyr)
4g.43030540A>GCA439192184GRXCR1c.873A>G (p.Ter291=)
c.510A>G (p.Ter170=)
4g.43030540A>TCA356792087GRXCR1c.873A>T (p.Ter291Tyr)
c.510A>T (p.Ter170Tyr)
4g.43030541T>CCA1061631188GRXCR1c.*1T>C (n.*1T>C)
c.874T>C (n.874T>C)
dbSNP gnomAD v3 gnomAD v4
4g.43030541T=CA1453107697GRXCR1c.*1T= (n.*1T=)
c.874T= (n.874T=)
4g.43030542T>CCA2705732732GRXCR1c.*2T>C (n.*2T>C)
c.875T>C (n.875T>C)
dbSNP
4g.43030546G>ACA1453107699GRXCR1c.*6G>A (n.*6G>A)
c.879G>A (n.879G>A)
dbSNP
4g.43030546G=CA1453107698GRXCR1c.*6G= (n.*6G=)
c.879G= (n.879G=)
4g.43030546G>TCA551142783GRXCR1c.*6G>T (n.*6G>T)
c.879G>T (n.879G>T)
ClinVar dbSNP gnomAD v2 gnomAD v4
4g.43030547C>ACA1453107701GRXCR1c.*7C>A (n.*7C>A)
c.880C>A (n.880C>A)
dbSNP
4g.43030547C=CA1453107700GRXCR1c.*7C= (n.*7C=)
c.880C= (n.880C=)
4g.43030547C>TCA2670496248GRXCR1c.*7C>T (n.*7C>T)
c.880C>T (n.880C>T)
gnomAD v4

Number of alleles fetched