Primary Site >> Stomach Cancer
Gene >> USP39
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323701 |
| Start | 85630848:85630848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.851T>A |
| AA Mutation | p.Leu284His(p.L284H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323701 |
| Start | 85616452:85616452(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.257G>A |
| AA Mutation | p.Arg86Gln(p.R86Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323701 |
| Start | 85625657:85625657(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.689T>C |
| AA Mutation | p.Ile230Thr(p.I230T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000323701 |
| Start | 85630824:85630824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.827G>A |
| AA Mutation | p.Arg276His(p.R276H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000323701 |
| Start | 85621542:85621542(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373537425 |
| CDS Mutation | c.396T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000323701 |
| Start | 85625580:85625580(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.612C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000323701 |
| Start | 85619269:85619269(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753735784 |
| CDS Mutation | c.318G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |