Primary Site >> Esophagus Cancer
Gene >> TIAM1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31130281:31130281(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3977G>T |
| AA Mutation | p.Trp1326Leu(p.W1326L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31223452:31223452(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1949C>T |
| AA Mutation | p.Ala650Val(p.A650V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31182569:31182569(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2739T>A |
| AA Mutation | p.Asp913Glu(p.D913E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000286827 |
| Start | 31130891:31130891(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3941T>G |
| AA Mutation | p.Leu1314Arg(p.L1314R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286827 |
| Start | 31153078:31153078(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3228C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286827 |
| Start | 31165025:31165025(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs557120271 |
| CDS Mutation | c.2928C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286827 |
| Start | 31252019:31252019(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374340137 |
| CDS Mutation | c.1134G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained;splice_region_variant |
| Transcription ID | ENST00000286827 |
| Start | 31266012:31266012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.961C>T |
| AA Mutation | p.Gln321Ter(p.Q321*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |