Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.136114925C>TCA1890055CXCR4c.991G>A (p.Gly331Ser)
c.958G>A (p.Gly320Ser)
c.1003G>A (p.Gly335Ser)
c.1015G>A (p.Gly339Ser)
n.1197G>A
c.1216G>A (p.Gly406Ser)
c.1102G>A (p.Gly368Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.136114925C>ACA348657456CXCR4c.991G>T (p.Gly331Cys)
c.958G>T (p.Gly320Cys)
c.1003G>T (p.Gly335Cys)
c.1015G>T (p.Gly339Cys)
n.1197G>T
c.1216G>T (p.Gly406Cys)
c.1102G>T (p.Gly368Cys)
dbSNP

Number of alleles fetched