Primary Site >> Stomach Cancer
Gene >> CCNB2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288207 |
| Start | 59124789:59124789(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1109G>A |
| AA Mutation | p.Ser370Asn(p.S370N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |