Primary Site >> Pancreatic Cancer
Gene >> EPHB4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358173 |
| Start | 100806538:100806538(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753075600 |
| CDS Mutation | c.2366C>T |
| AA Mutation | p.Pro789Leu(p.P789L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358173 |
| Start | 100822421:100822421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.658G>A |
| AA Mutation | p.Ala220Thr(p.A220T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358173 |
| Start | 100823888:100823888(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.167G>A |
| AA Mutation | p.Arg56His(p.R56H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358173 |
| Start | 100805262:100805262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2738G>A |
| AA Mutation | p.Gly913Asp(p.G913D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358173 |
| Start | 100817226:100817226(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148818692 |
| CDS Mutation | c.1554C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358173 |
| Start | 100822488:100822488(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.591C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358173 |
| Start | 100823728:100823728(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.327G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |