Primary Site >> Esophagus Cancer
Gene >> MSH2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000233146 |
| Start | 47475075:47475075(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1810G>A |
| AA Mutation | p.Ala604Thr(p.A604T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |