Primary Site >> Stomach Cancer
Gene >> RCVRN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000226193 |
| Start | 9901039:9901039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374805649 |
| CDS Mutation | c.443C>T |
| AA Mutation | p.Pro148Leu(p.P148L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000226193 |
| Start | 9901057:9901057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.425C>T |
| AA Mutation | p.Pro142Leu(p.P142L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000226193 |
| Start | 9904905:9904905(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.276G>C |
| AA Mutation | p.Met92Ile(p.M92I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000226193 |
| Start | 9901025:9901025(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754840876 |
| CDS Mutation | c.457G>A |
| AA Mutation | p.Glu153Lys(p.E153K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000226193 |
| Start | 9904835:9904835(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.346A>G |
| AA Mutation | p.Thr116Ala(p.T116A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000226193 |
| Start | 9904947:9904947(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.234C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000226193 |
| Start | 9904854:9904854(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761525513 |
| CDS Mutation | c.327C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |