Primary Site >> Stomach Cancer
Gene >> CAB39L
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347776 |
| Start | 49350905:49350905(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.403G>A |
| AA Mutation | p.Ala135Thr(p.A135T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347776 |
| Start | 49344210:49344210(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.593T>C |
| AA Mutation | p.Val198Ala(p.V198A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000347776 |
| Start | 49331974:49331974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.807C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000347776 |
| Start | 49359824:49359824(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.285delA |
| AA Mutation | p.Asp96MetfsTer2(p.D96Mfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000347776 |
| Start | 49331950:49331950(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.831delT |
| AA Mutation | p.Phe277LeufsTer19(p.F277Lfs*19) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000347776 |
| Start | 49350857:49350857(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200343559 |
| CDS Mutation | c.451C>T |
| AA Mutation | p.Arg151Ter(p.R151*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000347776 |
| Start | 49344177:49344178(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.624+1_624+2delGT |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |