Primary Site >> Stomach Cancer
Gene >> PPARD
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311565 |
| Start | 35424428:35424428(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.727G>A |
| AA Mutation | p.Val243Met(p.V243M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311565 |
| Start | 35425993:35425993(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1240G>A |
| AA Mutation | p.Ala414Thr(p.A414T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311565 |
| Start | 35424342:35424342(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.641A>T |
| AA Mutation | p.His214Leu(p.H214L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311565 |
| Start | 35424474:35424474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750380211 |
| CDS Mutation | c.773G>A |
| AA Mutation | p.Arg258Gln(p.R258Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311565 |
| Start | 35424662:35424662(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.961C>T |
| AA Mutation | p.Arg321Cys(p.R321C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311565 |
| Start | 35426029:35426029(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1276G>A |
| AA Mutation | p.Glu426Lys(p.E426K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311565 |
| Start | 35421871:35421871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201653737 |
| CDS Mutation | c.337C>T |
| AA Mutation | p.Arg113Cys(p.R113C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |