Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.136114915G>T | CA348657412 | CXCR4 | c.1001C>A (p.Ser334Ter) c.968C>A (p.Ser323Ter) c.1013C>A (p.Ser338Ter) c.1025C>A (p.Ser342Ter) n.1207C>A c.1226C>A (p.Ser409Ter) c.1112C>A (p.Ser371Ter) | ClinVar dbSNP gnomAD v4 COSMIC |
2 | g.136114915G>C | CA123717 | CXCR4 | c.1001C>G (p.Ser334Ter) c.968C>G (p.Ser323Ter) c.1013C>G (p.Ser338Ter) c.1025C>G (p.Ser342Ter) n.1207C>G c.1226C>G (p.Ser409Ter) c.1112C>G (p.Ser371Ter) | ClinVar dbSNP COSMIC |