Primary Site >> Stomach Cancer
Gene >> TRIB3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217233 |
| Start | 391329:391329(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.334G>A |
| AA Mutation | p.Ala112Thr(p.A112T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217233 |
| Start | 388186:388186(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.176C>T |
| AA Mutation | p.Ala59Val(p.A59V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217233 |
| Start | 396289:396289(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200530153 |
| CDS Mutation | c.676G>A |
| AA Mutation | p.Val226Met(p.V226M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217233 |
| Start | 396564:396564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.951G>C |
| AA Mutation | p.Gln317His(p.Q317H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217233 |
| Start | 388096:388096(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142361535 |
| CDS Mutation | c.86G>A |
| AA Mutation | p.Arg29His(p.R29H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217233 |
| Start | 396433:396433(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200373395 |
| CDS Mutation | c.820C>T |
| AA Mutation | p.Arg274Cys(p.R274C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217233 |
| Start | 388071:388071(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.61T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217233 |
| Start | 391457:391457(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.462C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |