Primary Site >> Stomach Cancer
Gene >> GTF2I
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000573035 |
| Start | 74753154:74753154(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2618A>C |
| AA Mutation | p.Asn873Thr(p.N873T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000573035 |
| Start | 74753121:74753121(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2585T>C |
| AA Mutation | p.Val862Ala(p.V862A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000573035 |
| Start | 74745896:74745896(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1948A>T |
| AA Mutation | p.Ile650Phe(p.I650F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000573035 |
| Start | 74714902:74714902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781866719 |
| CDS Mutation | c.809C>T |
| AA Mutation | p.Ser270Leu(p.S270L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000573035 |
| Start | 74699082:74699082(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.360C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000573035 |
| Start | 74700609:74700609(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.566delT |
| AA Mutation | p.Leu189Ter(p.L189*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | inframe_deletion;splice_region_variant |
| Transcription ID | ENST00000573035 |
| Start | 74716946:74716948(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.878_880delAAG |
| AA Mutation | p.Glu293del(p.E293del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |