Primary Site >> Pancreatic Cancer
Gene >> TYR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263321 |
| Start | 89191275:89191275(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148815276 |
| CDS Mutation | c.893G>A |
| AA Mutation | p.Arg298Gln(p.R298Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263321 |
| Start | 89191340:89191340(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.958T>G |
| AA Mutation | p.Phe320Val(p.F320V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263321 |
| Start | 89191404:89191404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1022G>T |
| AA Mutation | p.Arg341Ile(p.R341I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263321 |
| Start | 89284802:89284802(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772173320 |
| CDS Mutation | c.1214G>A |
| AA Mutation | p.Arg405His(p.R405H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263321 |
| Start | 89178418:89178418(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775182073 |
| CDS Mutation | c.465C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263321 |
| Start | 89295333:89295333(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs563119570 |
| CDS Mutation | c.1557G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |