Primary Site >> Stomach Cancer
Gene >> LGR5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266674 |
| Start | 71440124:71440124(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.44T>C |
| AA Mutation | p.Leu15Pro(p.L15P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000266674 |
| Start | 71580421:71580421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1550A>G |
| AA Mutation | p.Gln517Arg(p.Q517R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266674 |
| Start | 71440184:71440184(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.104C>T |
| AA Mutation | p.Pro35Leu(p.P35L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266674 |
| Start | 71584496:71584496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2486A>G |
| AA Mutation | p.Glu829Gly(p.E829G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266674 |
| Start | 71583832:71583832(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1822G>A |
| AA Mutation | p.Val608Ile(p.V608I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266674 |
| Start | 71582461:71582461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145133989 |
| CDS Mutation | c.1558C>T |
| AA Mutation | p.Arg520Cys(p.R520C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000266674 |
| Start | 71584098:71584098(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376301601 |
| CDS Mutation | c.2088C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000266674 |
| Start | 71583944:71583944(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1938delT |
| AA Mutation | p.Phe646LeufsTer21(p.F646Lfs*21) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000266674 |
| Start | 71440278:71440281(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.198_201delCTTC |
| AA Mutation | p.Phe67ProfsTer4(p.F67Pfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000266674 |
| Start | 71583933:71583933(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs753933845 |
| CDS Mutation | c.1928delT |
| AA Mutation | p.Leu643CysfsTer24(p.L643Cfs*24) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000266674 |
| Start | 71583886:71583886(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780252667 |
| CDS Mutation | c.1876C>T |
| AA Mutation | p.Arg626Ter(p.R626*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |