Primary Site >> Stomach Cancer
Gene >> PPARA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262735 |
| Start | 46215295:46215295(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.331G>T |
| AA Mutation | p.Gly111Cys(p.G111C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262735 |
| Start | 46235147:46235147(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1174C>A |
| AA Mutation | p.Leu392Ile(p.L392I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262735 |
| Start | 46215265:46215265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.301G>A |
| AA Mutation | p.Glu101Lys(p.E101K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262735 |
| Start | 46218285:46218285(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs549236046 |
| CDS Mutation | c.392G>A |
| AA Mutation | p.Arg131Gln(p.R131Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262735 |
| Start | 46232014:46232014(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.934G>A |
| AA Mutation | p.Gly312Arg(p.G312R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262735 |
| Start | 46232130:46232130(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751185249 |
| CDS Mutation | c.1050G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262735 |
| Start | 46218385:46218385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779053935 |
| CDS Mutation | c.492C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000262735 |
| Start | 46215322:46215322(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.358G>T |
| AA Mutation | p.Glu120Ter(p.E120*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |