Primary Site >> Pancreatic Cancer
Gene >> EPHB2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400191 |
| Start | 22912550:22912550(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757472320 |
| CDS Mutation | c.2803G>A |
| AA Mutation | p.Ala935Thr(p.A935T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400191 |
| Start | 22784429:22784429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202156735 |
| CDS Mutation | c.164C>T |
| AA Mutation | p.Thr55Met(p.T55M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400191 |
| Start | 22895577:22895577(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1697A>G |
| AA Mutation | p.Asn566Ser(p.N566S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400191 |
| Start | 22913860:22913860(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3158G>A |
| AA Mutation | p.Cys1053Tyr(p.C1053Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000400191 |
| Start | 22864959:22864959(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759784190 |
| CDS Mutation | c.1050C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000400191 |
| Start | 22913546:22913546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2937C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000400191 |
| Start | 22784877:22784877(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.612C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |