| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.136114925C>T | CA1890055 | CXCR4 | c.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 |
| 2 | g.136114925C>A | CA348657456 | CXCR4 | c.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 |
| 2 | g.136114925C= | CA1290965880 | CXCR4 | c.991G= (p.Gly331=) c.958G= (p.Gly320=) c.1003G= (p.Gly335=) c.1015G= (p.Gly339=) n.1197G= c.1216G= (p.Gly406=) c.1102G= (p.Gly368=) | dbSNP |