Primary Site >> Stomach Cancer
Gene >> VEZT
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000436874 |
| Start | 95300455:95300455(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2122A>G |
| AA Mutation | p.Thr708Ala(p.T708A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000436874 |
| Start | 95263066:95263066(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.419C>T |
| AA Mutation | p.Ala140Val(p.A140V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000436874 |
| Start | 95274849:95274849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.956C>T |
| AA Mutation | p.Ala319Val(p.A319V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000436874 |
| Start | 95266584:95266584(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.662C>T |
| AA Mutation | p.Ala221Val(p.A221V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000436874 |
| Start | 95263064:95263064(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.417G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000436874 |
| Start | 95270163:95270163(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.823C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000436874 |
| Start | 95257193:95257193(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs769992224 |
| CDS Mutation | c.220delT |
| AA Mutation | p.Ser74LeufsTer38(p.S74Lfs*38) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000436874 |
| Start | 95270162:95270163(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.822_823insT |
| AA Mutation | p.Leu275SerfsTer15(p.L275Sfs*15) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000436874 |
| Start | 95266512:95266513(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.597dupA |
| AA Mutation | p.Tyr200IlefsTer17(p.Y200Ifs*17) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |