Primary Site >> Esophagus Cancer
Gene >> EPHB2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400191 |
| Start | 22910487:22910487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2608C>T |
| AA Mutation | p.Arg870Trp(p.R870W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400191 |
| Start | 22863142:22863142(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750776222 |
| CDS Mutation | c.917G>A |
| AA Mutation | p.Arg306His(p.R306H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000400191 |
| Start | 22913502:22913502(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2899delA |
| AA Mutation | p.Ile967SerfsTer2(p.I967Sfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000400191 |
| Start | 22865012:22865032(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1105_1125delCGGGGTGCCTGCACCCGCTGC |
| AA Mutation | p.Arg369_Cys375del(p.R369_C375del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |