Primary Site >> Stomach Cancer
Gene >> CPE
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402744 |
| Start | 165482353:165482353(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376055726 |
| CDS Mutation | c.784C>T |
| AA Mutation | p.Arg262Trp(p.R262W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402744 |
| Start | 165379346:165379346(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.125G>A |
| AA Mutation | p.Arg42Gln(p.R42Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402744 |
| Start | 165482320:165482320(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.751G>T |
| AA Mutation | p.Asp251Tyr(p.D251Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402744 |
| Start | 165495607:165495607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1262T>G |
| AA Mutation | p.Leu421Arg(p.L421R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402744 |
| Start | 165464395:165464395(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780646997 |
| CDS Mutation | c.313C>T |
| AA Mutation | p.Pro105Ser(p.P105S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000402744 |
| Start | 165484459:165484459(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.828C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |