Primary Site >> Stomach Cancer
Gene >> NDE1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396355 |
| Start | 15687422:15687422(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.434C>T |
| AA Mutation | p.Ala145Val(p.A145V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396355 |
| Start | 15691218:15691218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.598G>A |
| AA Mutation | p.Glu200Lys(p.E200K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000396355 |
| Start | 15696774:15696774(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.861T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000396355 |
| Start | 15694205:15694205(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs1123418 |
| CDS Mutation | c.744G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000396355 |
| Start | 15691247:15691247(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768268553 |
| CDS Mutation | c.627G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000396355 |
| Start | 15694189:15694189(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs749768828 |
| CDS Mutation | c.733delC |
| AA Mutation | p.Leu245SerfsTer113(p.L245Sfs*113) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000396355 |
| Start | 15694182:15694182(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.726delG |
| AA Mutation | p.Thr243ProfsTer115(p.T243Pfs*115) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |