Primary Site >> Stomach Cancer
Gene >> COPS2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000388901 |
| Start | 49130722:49130722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1042G>A |
| AA Mutation | p.Glu348Lys(p.E348K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000388901 |
| Start | 49139602:49139602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745372669 |
| CDS Mutation | c.298C>T |
| AA Mutation | p.Arg100Trp(p.R100W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000388901 |
| Start | 49144267:49144267(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.206T>G |
| AA Mutation | p.Phe69Cys(p.F69C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000388901 |
| Start | 49134072:49134072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.752T>G |
| AA Mutation | p.Phe251Cys(p.F251C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000388901 |
| Start | 49139603:49139603(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.297T>G |
| AA Mutation | p.Ile99Met(p.I99M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000388901 |
| Start | 49133803:49133803(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148364582 |
| CDS Mutation | c.903G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000388901 |
| Start | 49134047:49134047(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.777delT |
| AA Mutation | p.Phe259LeufsTer19(p.F259Lfs*19) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000388901 |
| Start | 49134046:49134047(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.777dupT |
| AA Mutation | p.Glu260Ter(p.E260*) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000388901 |
| Start | 49134484:49134485(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.570dupA |
| AA Mutation | p.Gly191ArgfsTer21(p.G191Rfs*21) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |