Primary Site >> Pancreatic Cancer
Gene >> ARHGAP9
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393791 |
| Start | 57479319:57479319(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.88C>T |
| AA Mutation | p.Leu30Phe(p.L30F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000393791 |
| Start | 57477460:57477460(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147287939 |
| CDS Mutation | c.755C>T |
| AA Mutation | p.Thr252Met(p.T252M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | stop_gained;protein_altering_variant |
| Transcription ID | ENST00000393791 |
| Start | 57476607:57476608(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1007_1008insTTCCTA |
| AA Mutation | p.Gln336delinsHisSerTer(p.Q336delinsHS*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |