Primary Site >> Stomach Cancer
Gene >> LAMP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332556 |
| Start | 113306553:113306553(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.130G>A |
| AA Mutation | p.Ala44Thr(p.A44T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332556 |
| Start | 113310813:113310813(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.508C>A |
| AA Mutation | p.Leu170Ile(p.L170I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332556 |
| Start | 113321646:113321646(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767683537 |
| CDS Mutation | c.1033C>T |
| AA Mutation | p.Arg345Cys(p.R345C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332556 |
| Start | 113321590:113321590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767455348 |
| CDS Mutation | c.977G>A |
| AA Mutation | p.Arg326Gln(p.R326Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332556 |
| Start | 113306501:113306501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766554441 |
| CDS Mutation | c.78G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332556 |
| Start | 113320404:113320404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373542595 |
| CDS Mutation | c.810C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332556 |
| Start | 113319518:113319518(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs545159189 |
| CDS Mutation | c.612G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |