Primary Site >> Stomach Cancer
Gene >> MLXIP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319080 |
| Start | 122138512:122138512(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756776307 |
| CDS Mutation | c.2345G>A |
| AA Mutation | p.Arg782Gln(p.R782Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319080 |
| Start | 122130040:122130040(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.838G>A |
| AA Mutation | p.Glu280Lys(p.E280K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319080 |
| Start | 122130083:122130083(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755900622 |
| CDS Mutation | c.881C>T |
| AA Mutation | p.Pro294Leu(p.P294L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319080 |
| Start | 122138872:122138872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2442T>A |
| AA Mutation | p.Asp814Glu(p.D814E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319080 |
| Start | 122141015:122141015(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2570T>C |
| AA Mutation | p.Leu857Pro(p.L857P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319080 |
| Start | 122129147:122129147(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748755787 |
| CDS Mutation | c.617C>T |
| AA Mutation | p.Thr206Met(p.T206M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000319080 |
| Start | 122133431:122133431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1176T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000319080 |
| Start | 122133578:122133578(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776624139 |
| CDS Mutation | c.1323C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000319080 |
| Start | 122135256:122135257(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1765_1766delAT |
| AA Mutation | p.Met589AspfsTer139(p.M589Dfs*139) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |