Primary Site >> Stomach Cancer
Gene >> REM1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000201979 |
| Start | 31476640:31476640(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.195T>A |
| AA Mutation | p.Asp65Glu(p.D65E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000201979 |
| Start | 31476689:31476689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141530884 |
| CDS Mutation | c.244C>T |
| AA Mutation | p.Arg82Cys(p.R82C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000201979 |
| Start | 31482423:31482423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779937636 |
| CDS Mutation | c.560A>G |
| AA Mutation | p.His187Arg(p.H187R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000201979 |
| Start | 31476545:31476545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.100A>C |
| AA Mutation | p.Ser34Arg(p.S34R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000201979 |
| Start | 31476598:31476598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.153C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000201979 |
| Start | 31484247:31484247(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.714C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000201979 |
| Start | 31477883:31477883(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147559982 |
| CDS Mutation | c.396C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000201979 |
| Start | 31476466:31476466(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.21G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000201979 |
| Start | 31484311:31484331(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.780_800delGCCGGCCAGCCTAGCCCAGCG |
| AA Mutation | p.Pro261_Arg267del(p.P261_R267del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |