Primary Site >> Stomach Cancer
Gene >> SETDB2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354234 |
| Start | 49482932:49482932(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367576307 |
| CDS Mutation | c.1388A>G |
| AA Mutation | p.Lys463Arg(p.K463R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354234 |
| Start | 49482851:49482851(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1307G>T |
| AA Mutation | p.Cys436Phe(p.C436F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000354234 |
| Start | 49460109:49460109(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776253482 |
| CDS Mutation | c.19G>A |
| AA Mutation | p.Asp7Asn(p.D7N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000354234 |
| Start | 49491834:49491834(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs775302281 |
| CDS Mutation | c.2152delA |
| AA Mutation | p.Ile718TyrfsTer11(p.I718Yfs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000354234 |
| Start | 49451901:49451901(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.14delA |
| AA Mutation | p.Asn5MetfsTer11(p.N5Mfs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000354234 |
| Start | 49488583:49488583(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1910delT |
| AA Mutation | p.Leu637TyrfsTer29(p.L637Yfs*29) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000354234 |
| Start | 49483555:49483555(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs768645211 |
| CDS Mutation | c.1516delA |
| AA Mutation | p.Met506TrpfsTer24(p.M506Wfs*24) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000354234 |
| Start | 49488475:49488475(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs184575306 |
| CDS Mutation | c.1798C>T |
| AA Mutation | p.Arg600Ter(p.R600*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |