Primary Site >> Pancreatic Cancer
Gene >> FHOD3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359247 |
| Start | 36625616:36625616(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1063C>T |
| AA Mutation | p.Arg355Trp(p.R355W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359247 |
| Start | 36355627:36355627(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768664285 |
| CDS Mutation | c.254G>A |
| AA Mutation | p.Gly85Asp(p.G85D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359247 |
| Start | 36625713:36625713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1160G>A |
| AA Mutation | p.Ser387Asn(p.S387N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359247 |
| Start | 36730757:36730757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2953G>A |
| AA Mutation | p.Ala985Thr(p.A985T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000359247 |
| Start | 36372682:36372682(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769863952 |
| CDS Mutation | c.275G>A |
| AA Mutation | p.Arg92Gln(p.R92Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359247 |
| Start | 36709228:36709228(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1794A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |