Primary Site >> Pancreatic Cancer
Gene >> ABL1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372348 |
| Start | 130714360:130714360(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.41G>T |
| AA Mutation | p.Arg14Met(p.R14M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372348 |
| Start | 130714423:130714423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.104G>T |
| AA Mutation | p.Gly35Val(p.G35V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318560 |
| Start | 130854938:130854938(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.391C>T |
| AA Mutation | p.Pro131Ser(p.P131S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318560 |
| Start | 130880104:130880104(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1460C>A |
| AA Mutation | p.Ala487Asp(p.A487D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318560 |
| Start | 130884087:130884087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1797G>C |
| AA Mutation | p.Leu599Phe(p.L599F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318560 |
| Start | 130885403:130885403(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367600262 |
| CDS Mutation | c.3113C>T |
| AA Mutation | p.Ala1038Val(p.A1038V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000318560 |
| Start | 130885315:130885315(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3025C>T |
| AA Mutation | p.Arg1009Ter(p.R1009*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |