Primary Site >> Pancreatic Cancer
Gene >> NOTCH1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000277541 |
| Start | 136497438:136497438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6301G>A |
| AA Mutation | p.Ala2101Thr(p.A2101T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000277541 |
| Start | 136503230:136503230(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5119G>A |
| AA Mutation | p.Ala1707Thr(p.A1707T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000277541 |
| Start | 136511241:136511241(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2498G>A |
| AA Mutation | p.Cys833Tyr(p.C833Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000277541 |
| Start | 136517788:136517788(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1405G>T |
| AA Mutation | p.Asp469Tyr(p.D469Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000277541 |
| Start | 136517836:136517836(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761629787 |
| CDS Mutation | c.1357G>A |
| AA Mutation | p.Val453Ile(p.V453I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000277541 |
| Start | 136517846:136517846(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1347C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000277541 |
| Start | 136500834:136500834(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766279504 |
| CDS Mutation | c.5652G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |