Primary Site >> Stomach Cancer
Gene >> VCL
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000211998 |
| Start | 74111910:74111910(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143321584 |
| CDS Mutation | c.2747C>T |
| AA Mutation | p.Pro916Leu(p.P916L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000211998 |
| Start | 74094354:74094354(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1436G>A |
| AA Mutation | p.Arg479Gln(p.R479Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000211998 |
| Start | 74090092:74090092(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746004026 |
| CDS Mutation | c.1246C>T |
| AA Mutation | p.Arg416Trp(p.R416W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000211998 |
| Start | 74089209:74089209(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1036T>C |
| AA Mutation | p.Ser346Pro(p.S346P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000211998 |
| Start | 74095685:74095685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1573G>A |
| AA Mutation | p.Glu525Lys(p.E525K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000211998 |
| Start | 74105241:74105241(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202184524 |
| CDS Mutation | c.2322C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000211998 |
| Start | 74105238:74105238(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2319T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000211998 |
| Start | 74074882:74074882(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.762T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000211998 |
| Start | 74108985:74108985(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2574T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000211998 |
| Start | 74118067:74118067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3303T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000211998 |
| Start | 74112070:74112070(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2907G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000211998 |
| Start | 74109015:74109015(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2604T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000211998 |
| Start | 74105110:74105110(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2196delA |
| AA Mutation | p.Asp733ThrfsTer7(p.D733Tfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000211998 |
| Start | 74082539:74082539(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.872delC |
| AA Mutation | p.Pro291GlnfsTer13(p.P291Qfs*13) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000211998 |
| Start | 74072792:74072792(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs397517244 |
| CDS Mutation | c.562C>T |
| AA Mutation | p.Arg188Ter(p.R188*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |