Primary Site >> Pancreatic Cancer
Gene >> NOTCH3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263388 |
| Start | 15165902:15165902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5552G>A |
| AA Mutation | p.Arg1851His(p.R1851H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263388 |
| Start | 15174078:15174078(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4726G>A |
| AA Mutation | p.Glu1576Lys(p.E1576K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263388 |
| Start | 15185304:15185304(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2249G>T |
| AA Mutation | p.Ser750Ile(p.S750I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263388 |
| Start | 15185390:15185390(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2163G>T |
| AA Mutation | p.Glu721Asp(p.E721D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263388 |
| Start | 15189067:15189067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1300G>A |
| AA Mutation | p.Glu434Lys(p.E434K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263388 |
| Start | 15160696:15160696(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771682246 |
| CDS Mutation | c.6932C>T |
| AA Mutation | p.Pro2311Leu(p.P2311L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263388 |
| Start | 15161016:15161016(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752030208 |
| CDS Mutation | c.6612G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263388 |
| Start | 15160962:15160962(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769365145 |
| CDS Mutation | c.6666G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263388 |
| Start | 15180976:15180976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2979G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000263388 |
| Start | 15184451:15184451(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2411-1G>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |