Primary Site >> Stomach Cancer
Gene >> USP5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229268 |
| Start | 6855466:6855466(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.177G>T |
| AA Mutation | p.Glu59Asp(p.E59D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229268 |
| Start | 6855485:6855485(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782121425 |
| CDS Mutation | c.196G>A |
| AA Mutation | p.Gly66Ser(p.G66S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229268 |
| Start | 6861592:6861592(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1648C>A |
| AA Mutation | p.Leu550Met(p.L550M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229268 |
| Start | 6861085:6861085(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1477A>G |
| AA Mutation | p.Met493Val(p.M493V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000229268 |
| Start | 6855436:6855436(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782659504 |
| CDS Mutation | c.147G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000229268 |
| Start | 6865222:6865222(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200493713 |
| CDS Mutation | c.2457C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000229268 |
| Start | 6866029:6866029(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372777292 |
| CDS Mutation | c.2529G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000229268 |
| Start | 6859509:6859509(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143750403 |
| CDS Mutation | c.1098G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000229268 |
| Start | 6863888:6863888(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782022808 |
| CDS Mutation | c.2013C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000229268 |
| Start | 6864114:6864114(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2168delC |
| AA Mutation | p.Pro723LeufsTer6(p.P723Lfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |