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
2g.136114915G=CA1290965875CXCR4c.1001C= (p.Ser334=)
c.968C= (p.Ser323=)
c.1013C= (p.Ser338=)
c.1025C= (p.Ser342=)
n.1207C=
c.1226C= (p.Ser409=)
c.1112C= (p.Ser371=)
dbSNP

Number of alleles fetched