Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.42962919C>TCA114035GRXCR1c.412C>T (p.Arg138Cys)
c.49C>T (p.Arg17Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.42962919C=CA1453073740GRXCR1c.412C= (p.Arg138=)
c.49C= (p.Arg17=)
 dbSNP

Number of alleles fetched