Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.136114915G>TCA348657412CXCR4c.1001C>A (p.Ser334Ter)
c.968C>A (p.Ser323Ter)
c.1013C>A (p.Ser338Ter)
c.1025C>A (p.Ser342Ter)
n.1207C>A
c.1226C>A (p.Ser409Ter)
c.1112C>A (p.Ser371Ter)
ClinVar dbSNP gnomAD v4 COSMIC
2g.136114915G>CCA123717CXCR4c.1001C>G (p.Ser334Ter)
c.968C>G (p.Ser323Ter)
c.1013C>G (p.Ser338Ter)
c.1025C>G (p.Ser342Ter)
n.1207C>G
c.1226C>G (p.Ser409Ter)
c.1112C>G (p.Ser371Ter)
ClinVar dbSNP COSMIC

Number of alleles fetched