Primary Site >> Stomach Cancer
Gene >> MSX1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382723 |
| Start | 4862854:4862854(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.623C>T |
| AA Mutation | p.Ser208Leu(p.S208L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382723 |
| Start | 4862901:4862901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.670C>T |
| AA Mutation | p.Arg224Cys(p.R224C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382723 |
| Start | 4862749:4862749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.518G>A |
| AA Mutation | p.Arg173His(p.R173H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382723 |
| Start | 4863124:4863124(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.893G>A |
| AA Mutation | p.Ser298Asn(p.S298N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382723 |
| Start | 4863011:4863011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.780C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382723 |
| Start | 4862837:4862837(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.606C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382723 |
| Start | 4862777:4862777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140353960 |
| CDS Mutation | c.546G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382723 |
| Start | 4862903:4862903(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.672C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000382723 |
| Start | 4862711:4862711(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs762477502 |
| CDS Mutation | c.485delC |
| AA Mutation | p.Pro162GlnfsTer55(p.P162Qfs*55) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |