Primary Site >> Stomach Cancer
Gene >> IDH3G
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217901 |
| Start | 153787515:153787515(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782789248 |
| CDS Mutation | c.623C>T |
| AA Mutation | p.Ala208Val(p.A208V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217901 |
| Start | 153786830:153786830(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.895T>C |
| AA Mutation | p.Tyr299His(p.Y299H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217901 |
| Start | 153787485:153787485(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.653C>T |
| AA Mutation | p.Ala218Val(p.A218V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217901 |
| Start | 153787534:153787534(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.604G>A |
| AA Mutation | p.Glu202Lys(p.E202K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217901 |
| Start | 153786888:153786888(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141309746 |
| CDS Mutation | c.837C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217901 |
| Start | 153788101:153788101(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782297826 |
| CDS Mutation | c.381G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |