Primary Site >> Stomach Cancer
Gene >> MGMT
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306010 |
| Start | 129708023:129708023(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.347A>G |
| AA Mutation | p.His116Arg(p.H116R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306010 |
| Start | 129759277:129759277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.443T>C |
| AA Mutation | p.Leu148Ser(p.L148S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306010 |
| Start | 129536260:129536260(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.101A>G |
| AA Mutation | p.Lys34Arg(p.K34R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306010 |
| Start | 129536278:129536278(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs544050191 |
| CDS Mutation | c.119G>A |
| AA Mutation | p.Arg40His(p.R40H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306010 |
| Start | 129536370:129536370(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.211G>A |
| AA Mutation | p.Ala71Thr(p.A71T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000306010 |
| Start | 129766989:129766989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756598334 |
| CDS Mutation | c.709C>T |
| AA Mutation | p.Arg237Ter(p.R237*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |