Primary Site >> Pancreatic Cancer
Gene >> TBC1D9
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442267 |
| Start | 140622412:140622412(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3584G>T |
| AA Mutation | p.Gly1195Val(p.G1195V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442267 |
| Start | 140622424:140622424(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755965461 |
| CDS Mutation | c.3572G>A |
| AA Mutation | p.Arg1191Gln(p.R1191Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442267 |
| Start | 140622659:140622659(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3337C>A |
| AA Mutation | p.Leu1113Met(p.L1113M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442267 |
| Start | 140668980:140668980(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759134525 |
| CDS Mutation | c.1525C>T |
| AA Mutation | p.Arg509Trp(p.R509W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442267 |
| Start | 140670815:140670815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1171C>A |
| AA Mutation | p.Leu391Ile(p.L391I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442267 |
| Start | 140701570:140701570(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746432332 |
| CDS Mutation | c.175C>T |
| AA Mutation | p.Arg59Trp(p.R59W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000442267 |
| Start | 140622222:140622222(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3774C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000442267 |
| Start | 140657756:140657756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1978C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |