Primary Site >> Stomach Cancer
Gene >> PTGDR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306051 |
| Start | 52268545:52268545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.731C>T |
| AA Mutation | p.Ala244Val(p.A244V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306051 |
| Start | 52268553:52268553(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199553417 |
| CDS Mutation | c.739C>T |
| AA Mutation | p.Arg247Cys(p.R247C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306051 |
| Start | 52268095:52268095(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.281G>T |
| AA Mutation | p.Arg94Leu(p.R94L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306051 |
| Start | 52268052:52268052(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.238A>G |
| AA Mutation | p.Ser80Gly(p.S80G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306051 |
| Start | 52268041:52268041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.227A>G |
| AA Mutation | p.Lys76Arg(p.K76R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306051 |
| Start | 52268410:52268410(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.596A>G |
| AA Mutation | p.Tyr199Cys(p.Y199C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306051 |
| Start | 52268384:52268384(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.570G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306051 |
| Start | 52268171:52268171(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.357G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306051 |
| Start | 52274736:52274736(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768208384 |
| CDS Mutation | c.852C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306051 |
| Start | 52268613:52268613(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.799C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306051 |
| Start | 52268123:52268123(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs552490333 |
| CDS Mutation | c.309G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |