Primary Site >> Stomach Cancer
Gene >> TCF4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356073 |
| Start | 55228309:55228309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1920G>T |
| AA Mutation | p.Lys640Asn(p.K640N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356073 |
| Start | 55228949:55228949(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1765C>T |
| AA Mutation | p.Arg589Cys(p.R589C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356073 |
| Start | 55254614:55254614(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774269559 |
| CDS Mutation | c.1233G>T |
| AA Mutation | p.Met411Ile(p.M411I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356073 |
| Start | 55228885:55228885(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1829C>T |
| AA Mutation | p.Ala610Val(p.A610V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356073 |
| Start | 55587082:55587082(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.35C>T |
| AA Mutation | p.Thr12Met(p.T12M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356073 |
| Start | 55279649:55279649(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778907139 |
| CDS Mutation | c.557C>T |
| AA Mutation | p.Ala186Val(p.A186V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356073 |
| Start | 55232550:55232550(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370405835 |
| CDS Mutation | c.1608C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356073 |
| Start | 55587087:55587087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.30A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000356073 |
| Start | 55585321:55585321(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.104delA |
| AA Mutation | p.Asn35MetfsTer16(p.N35Mfs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000356073 |
| Start | 55228289:55228289(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1940delC |
| AA Mutation | p.Pro647LeufsTer32(p.P647Lfs*32) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000356073 |
| Start | 55232519:55232519(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1637+2T>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000356073 |
| Start | 55257314:55257314(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs587784458 |
| CDS Mutation | c.1146+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |