Chr Mutation (hg38) CAid Gene Transcript Linkouts
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