Primary Site >> Stomach Cancer
Gene >> POLR2C
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219252 |
| Start | 57471031:57471031(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.740C>T |
| AA Mutation | p.Ser247Leu(p.S247L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219252 |
| Start | 57469282:57469282(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.376C>T |
| AA Mutation | p.Arg126Trp(p.R126W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219252 |
| Start | 57469210:57469210(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.304A>G |
| AA Mutation | p.Thr102Ala(p.T102A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000219252 |
| Start | 57471008:57471008(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.717G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000219252 |
| Start | 57469242:57469242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756373925 |
| CDS Mutation | c.336G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000219252 |
| Start | 57465997:57465998(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.182dupA |
| AA Mutation | p.Asp61GlufsTer2(p.D61Efs*2) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |