| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.136114928G>C | CA348657469 | CXCR4 | c.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 |
| 2 | g.136114928G>A | CA123711 | CXCR4 | c.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 |
| 2 | g.136114928G= | CA1290965882 | CXCR4 | c.988C= (p.Arg330=) c.955C= (p.Arg319=) c.1000C= (p.Arg334=) c.1012C= (p.Arg338=) n.1194C= c.1213C= (p.Arg405=) c.1099C= (p.Arg367=) | dbSNP |