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 |