Primary Site >> Stomach Cancer
Gene >> ATIC
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000236959 |
| Start | 215326891:215326891(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs549649169 |
| CDS Mutation | c.601G>A |
| AA Mutation | p.Val201Ile(p.V201I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000236959 |
| Start | 215349555:215349555(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372018177 |
| CDS Mutation | c.1679C>T |
| AA Mutation | p.Ala560Val(p.A560V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000236959 |
| Start | 215333451:215333451(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.916G>A |
| AA Mutation | p.Ala306Thr(p.A306T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000236959 |
| Start | 215332416:215332416(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143393493 |
| CDS Mutation | c.723C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000236959 |
| Start | 215318217:215318217(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.207T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000236959 |
| Start | 215344797:215344797(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs556853914 |
| CDS Mutation | c.1246C>T |
| AA Mutation | p.Arg416Ter(p.R416*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |