Primary Site >> Stomach Cancer
Gene >> GALNT2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366672 |
| Start | 230203166:230203166(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.250G>A |
| AA Mutation | p.Glu84Lys(p.E84K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000366672 |
| Start | 230243426:230243426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.728A>C |
| AA Mutation | p.Glu243Ala(p.E243A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366672 |
| Start | 230255317:230255317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376128700 |
| CDS Mutation | c.1109C>T |
| AA Mutation | p.Pro370Leu(p.P370L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366672 |
| Start | 230236067:230236067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.428C>T |
| AA Mutation | p.Thr143Met(p.T143M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366672 |
| Start | 230243331:230243331(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.633G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000366672 |
| Start | 230236668:230236668(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.553delG |
| AA Mutation | p.Ala185LeufsTer36(p.A185Lfs*36) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000366672 |
| Start | 230250459:230250459(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.912delC |
| AA Mutation | p.Met305Ter(p.M305*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000366672 |
| Start | 230236698:230236698(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750040941 |
| CDS Mutation | c.580C>T |
| AA Mutation | p.Arg194Ter(p.R194*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |