Primary Site >> Stomach Cancer
Gene >> MIIP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000235332 |
| Start | 12021751:12021751(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs555419682 |
| CDS Mutation | c.25C>G |
| AA Mutation | p.Gln9Glu(p.Q9E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000235332 |
| Start | 12029831:12029831(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373485692 |
| CDS Mutation | c.782G>A |
| AA Mutation | p.Arg261His(p.R261H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000235332 |
| Start | 12031289:12031289(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.966T>G |
| AA Mutation | p.Ile322Met(p.I322M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000235332 |
| Start | 12031788:12031788(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368120960 |
| CDS Mutation | c.1147G>A |
| AA Mutation | p.Val383Ile(p.V383I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000235332 |
| Start | 12022374:12022374(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.394G>T |
| AA Mutation | p.Gly132Cys(p.G132C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000235332 |
| Start | 12031799:12031799(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1158G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000235332 |
| Start | 12031754:12031754(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759492545 |
| CDS Mutation | c.1113G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000235332 |
| Start | 12031748:12031748(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770778672 |
| CDS Mutation | c.1107G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |