Primary Site >> Stomach Cancer
Gene >> CRP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255030 |
| Start | 159713728:159713728(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.472G>T |
| AA Mutation | p.Asp158Tyr(p.D158Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255030 |
| Start | 159713713:159713713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.487A>T |
| AA Mutation | p.Asn163Tyr(p.N163Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255030 |
| Start | 159713616:159713616(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.584G>A |
| AA Mutation | p.Gly195Asp(p.G195D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000255030 |
| Start | 159713983:159713983(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.217G>A |
| AA Mutation | p.Ala73Thr(p.A73T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000255030 |
| Start | 159713768:159713768(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.432T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000255030 |
| Start | 159713894:159713894(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369190068 |
| CDS Mutation | c.306C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |