Primary Site >> Stomach Cancer
Gene >> EFNB3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000226091 |
| Start | 7708152:7708152(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.317G>A |
| AA Mutation | p.Arg106His(p.R106H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000226091 |
| Start | 7708224:7708224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.389G>A |
| AA Mutation | p.Arg130His(p.R130H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000226091 |
| Start | 7709294:7709294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.741T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000226091 |
| Start | 7708228:7708228(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201844534 |
| CDS Mutation | c.393G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000226091 |
| Start | 7709214:7709214(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.665delC |
| AA Mutation | p.Pro222LeufsTer72(p.P222Lfs*72) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000226091 |
| Start | 7708118:7708118(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.287delC |
| AA Mutation | p.Pro96LeufsTer62(p.P96Lfs*62) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000226091 |
| Start | 7709250:7709250(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.702delG |
| AA Mutation | p.Leu235TrpfsTer59(p.L235Wfs*59) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000226091 |
| Start | 7709538:7709538(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.991delC |
| AA Mutation | p.Gln331ArgfsTer39(p.Q331Rfs*39) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000226091 |
| Start | 7709384:7709384(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.836delG |
| AA Mutation | p.Gly279ValfsTer15(p.G279Vfs*15) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000226091 |
| Start | 7709207:7709207(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.658delC |
| AA Mutation | p.Leu220CysfsTer74(p.L220Cfs*74) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000226091 |
| Start | 7705605:7705605(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.13delC |
| AA Mutation | p.His5IlefsTer54(p.H5Ifs*54) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000226091 |
| Start | 7709537:7709538(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs756422375 |
| CDS Mutation | c.991dupC |
| AA Mutation | p.Gln331ProfsTer20(p.Q331Pfs*20) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |