Primary Site >> Stomach Cancer
Gene >> TGIF2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373872 |
| Start | 36578932:36578932(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.158G>T |
| AA Mutation | p.Ser53Ile(p.S53I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373872 |
| Start | 36578904:36578904(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs538264393 |
| CDS Mutation | c.130G>A |
| AA Mutation | p.Ala44Thr(p.A44T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373872 |
| Start | 36578779:36578779(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764618617 |
| CDS Mutation | c.5C>T |
| AA Mutation | p.Ser2Leu(p.S2L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373872 |
| Start | 36578822:36578822(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748658479 |
| CDS Mutation | c.48G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000373872 |
| Start | 36591210:36591213(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.493_496delACTC |
| AA Mutation | p.Thr165CysfsTer2(p.T165Cfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000373872 |
| Start | 36591136:36591136(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.422delA |
| AA Mutation | p.Lys141SerfsTer18(p.K141Sfs*18) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |