Primary Site >> Stomach Cancer
Gene >> USP11
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000218348 |
| Start | 47244846:47244846(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2137C>T |
| AA Mutation | p.Arg713Cys(p.R713C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000218348 |
| Start | 47239476:47239476(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778641852 |
| CDS Mutation | c.541C>T |
| AA Mutation | p.Arg181Cys(p.R181C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000218348 |
| Start | 47247823:47247823(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760876517 |
| CDS Mutation | c.2785C>T |
| AA Mutation | p.Arg929Cys(p.R929C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000218348 |
| Start | 47239146:47239146(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.382C>A |
| AA Mutation | p.Pro128Thr(p.P128T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000218348 |
| Start | 47242636:47242636(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1628C>T |
| AA Mutation | p.Ala543Val(p.A543V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000218348 |
| Start | 47242289:47242289(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1516C>T |
| AA Mutation | p.Arg506Cys(p.R506C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000218348 |
| Start | 47241376:47241376(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1075G>A |
| AA Mutation | p.Ala359Thr(p.A359T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000218348 |
| Start | 47247641:47247641(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2696G>A |
| AA Mutation | p.Gly899Asp(p.G899D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000218348 |
| Start | 47233040:47233040(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.126G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000218348 |
| Start | 47242141:47242141(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1368C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000218348 |
| Start | 47240631:47240631(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767470264 |
| CDS Mutation | c.855C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000218348 |
| Start | 47244901:47244902(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2194dupA |
| AA Mutation | p.Thr732AsnfsTer4(p.T732Nfs*4) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |