Primary Site >> Stomach Cancer
Gene >> DLAT
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280346 |
| Start | 112051312:112051312(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782632175 |
| CDS Mutation | c.1477G>A |
| AA Mutation | p.Glu493Lys(p.E493K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280346 |
| Start | 112033459:112033459(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.716A>G |
| AA Mutation | p.Glu239Gly(p.E239G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280346 |
| Start | 112026252:112026252(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.334G>A |
| AA Mutation | p.Glu112Lys(p.E112K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000280346 |
| Start | 112045969:112045969(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1397A>C |
| AA Mutation | p.Lys466Thr(p.K466T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280346 |
| Start | 112028611:112028611(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782189104 |
| CDS Mutation | c.478G>A |
| AA Mutation | p.Gly160Arg(p.G160R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000280346 |
| Start | 112025652:112025652(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.180C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000280346 |
| Start | 112033459:112033459(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.723delA |
| AA Mutation | p.Val242TrpfsTer5(p.V242Wfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000280346 |
| Start | 112026253:112026253(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs782369906 |
| CDS Mutation | c.342delA |
| AA Mutation | p.Glu115ArgfsTer10(p.E115Rfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | splice_donor_variant;coding_sequence_variant;intron_variant |
| Transcription ID | ENST00000280346 |
| Start | 112045966:112045998(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1395_1398+29delTAAGGTAAAAGTTCTGAAAATTCCAACTTTCTA |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |