Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.43030451C>ACA439192131GRXCR1c.784C>A (p.Arg262=)
c.421C>A (p.Arg141=)
4g.43030451C=CA1453107660GRXCR1c.784C= (p.Arg262=)
c.421C= (p.Arg141=)
dbSNP
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=)
dbSNP
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=CA3117758293GRXCR1c.786A= (p.Arg262=)
c.423A= (p.Arg141=)
dbSNP
4g.43030453A>CCA439192132GRXCR1c.786A>C (p.Arg262=)
c.423A>C (p.Arg141=)
4g.43030453A>GCA439192133GRXCR1c.786A>G (p.Arg262=)
c.423A>G (p.Arg141=)
dbSNP 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=CA3117758299GRXCR1c.788A= (p.Asn263=)
c.425A= (p.Asn142=)
dbSNP
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)
dbSNP gnomAD v4
4g.43030456C>ACA356791899GRXCR1c.789C>A (p.Asn263Lys)
c.426C>A (p.Asn142Lys)
4g.43030456C=CA3117758321GRXCR1c.789C= (p.Asn263=)
c.426C= (p.Asn142=)
dbSNP
4g.43030456C>GCA356791900GRXCR1c.789C>G (p.Asn263Lys)
c.426C>G (p.Asn142Lys)
dbSNP 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)
dbSNP gnomAD v4
4g.43030457T>GCA356791902GRXCR1c.790T>G (p.Cys264Gly)
c.427T>G (p.Cys143Gly)
dbSNP gnomAD v4
4g.43030457T=CA3117758350GRXCR1c.790T= (p.Cys264=)
c.427T= (p.Cys143=)
dbSNP
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=)
dbSNP
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)
dbSNP gnomAD v4
4g.43030461T>GCA356791913GRXCR1c.794T>G (p.Phe265Cys)
c.431T>G (p.Phe144Cys)
4g.43030461T=CA3117758399GRXCR1c.794T= (p.Phe265=)
c.431T= (p.Phe144=)
dbSNP
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=)
dbSNP

Number of alleles fetched