Primary Site >> Stomach Cancer
Gene >> PHGDH
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369409 |
| Start | 119735390:119735390(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768347730 |
| CDS Mutation | c.739C>T |
| AA Mutation | p.Arg247Trp(p.R247W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369409 |
| Start | 119737205:119737205(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.884G>A |
| AA Mutation | p.Cys295Tyr(p.C295Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369409 |
| Start | 119735387:119735387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.736C>A |
| AA Mutation | p.Leu246Ile(p.L246I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369409 |
| Start | 119742916:119742916(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1319G>A |
| AA Mutation | p.Gly440Asp(p.G440D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369409 |
| Start | 119741799:119741799(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1111A>C |
| AA Mutation | p.Ser371Arg(p.S371R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369409 |
| Start | 119735355:119735355(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.704C>T |
| AA Mutation | p.Ala235Val(p.A235V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369409 |
| Start | 119721226:119721226(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771208719 |
| CDS Mutation | c.195C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained;splice_region_variant |
| Transcription ID | ENST00000369409 |
| Start | 119735441:119735441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.790G>T |
| AA Mutation | p.Glu264Ter(p.E264*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000369409 |
| Start | 119727038:119727055(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.447_464delAATTCTTGGCCTGGGCAG |
| AA Mutation | p.Leu151_Ile156del(p.L151_I156del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |