Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.136114928G>CCA348657469CXCR4c.988C>G (p.Arg330Gly)
c.955C>G (p.Arg319Gly)
c.1000C>G (p.Arg334Gly)
c.1012C>G (p.Arg338Gly)
n.1194C>G
c.1213C>G (p.Arg405Gly)
c.1099C>G (p.Arg367Gly)
ClinVar dbSNP gnomAD v4
2g.136114928G>ACA123711CXCR4c.988C>T (p.Arg330Ter)
c.955C>T (p.Arg319Ter)
c.1000C>T (p.Arg334Ter)
c.1012C>T (p.Arg338Ter)
n.1194C>T
c.1213C>T (p.Arg405Ter)
c.1099C>T (p.Arg367Ter)
ClinVar dbSNP COSMIC COSMIC

Number of alleles fetched