Primary Site >> Pancreatic Cancer
Gene >> NOTCH4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375023 |
| Start | 32195814:32195814(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5635G>A |
| AA Mutation | p.Ala1879Thr(p.A1879T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375023 |
| Start | 32199049:32199049(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4412T>G |
| AA Mutation | p.Ile1471Ser(p.I1471S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375023 |
| Start | 32204143:32204143(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3112C>G |
| AA Mutation | p.His1038Asp(p.H1038D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375023 |
| Start | 32196369:32196369(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5253C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375023 |
| Start | 32197305:32197305(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5046C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375023 |
| Start | 32204150:32204150(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3105G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |