Primary Site >> Stomach Cancer
Gene >> AKT1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349310 |
| Start | 104772375:104772375(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1250A>G |
| AA Mutation | p.Tyr417Cys(p.Y417C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349310 |
| Start | 104770769:104770769(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764514218 |
| CDS Mutation | c.1339A>G |
| AA Mutation | p.Ile447Val(p.I447V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349310 |
| Start | 104770360:104770360(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1424C>T |
| AA Mutation | p.Ser475Leu(p.S475L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000349310 |
| Start | 104780214:104780214(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121434592 |
| CDS Mutation | c.49G>A |
| AA Mutation | p.Glu17Lys(p.E17K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000349310 |
| Start | 104773042:104773042(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1008C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000349310 |
| Start | 104775655:104775655(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs17846825 |
| CDS Mutation | c.432C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000349310 |
| Start | 104772380:104772380(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758476416 |
| CDS Mutation | c.1245C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |