Primary Site >> Pancreatic Cancer
Gene >> TIAM1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31120744:31120744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201116117 |
| CDS Mutation | c.4400C>T |
| AA Mutation | p.Pro1467Leu(p.P1467L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31217605:31217605(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2090G>T |
| AA Mutation | p.Trp697Leu(p.W697L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31120498:31120498(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143032407 |
| CDS Mutation | c.4646G>A |
| AA Mutation | p.Arg1549His(p.R1549H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31154289:31154289(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3129G>T |
| AA Mutation | p.Lys1043Asn(p.K1043N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31252020:31252020(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1133C>T |
| AA Mutation | p.Ala378Val(p.A378V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31141377:31141377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3603G>T |
| AA Mutation | p.Arg1201Ser(p.R1201S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286827 |
| Start | 31165028:31165028(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2925G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286827 |
| Start | 31127109:31127109(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766297450 |
| CDS Mutation | c.4089C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |