Primary Site >> Stomach Cancer
Gene >> SEMA4G
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370250 |
| Start | 100980270:100980270(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764503702 |
| CDS Mutation | c.1277G>A |
| AA Mutation | p.Arg426His(p.R426H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370250 |
| Start | 100977678:100977678(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.383C>T |
| AA Mutation | p.Thr128Ile(p.T128I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370250 |
| Start | 100980242:100980242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367801117 |
| CDS Mutation | c.1249C>T |
| AA Mutation | p.Arg417Trp(p.R417W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370250 |
| Start | 100980172:100980172(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760713409 |
| CDS Mutation | c.1179G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370250 |
| Start | 100983528:100983528(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764912089 |
| CDS Mutation | c.1914C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370250 |
| Start | 100972990:100972990(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs571547734 |
| CDS Mutation | c.78G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370250 |
| Start | 100983426:100983426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764701072 |
| CDS Mutation | c.1812C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000370250 |
| Start | 100983521:100983521(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1910delA |
| AA Mutation | p.Asn637MetfsTer37(p.N637Mfs*37) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |