Primary Site >> Stomach Cancer
Gene >> USP10
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219473 |
| Start | 84778945:84778945(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779306261 |
| CDS Mutation | c.2260G>A |
| AA Mutation | p.Val754Ile(p.V754I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219473 |
| Start | 84778975:84778975(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2290C>T |
| AA Mutation | p.Arg764Cys(p.R764C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219473 |
| Start | 84758746:84758746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1223A>C |
| AA Mutation | p.Lys408Thr(p.K408T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219473 |
| Start | 84772589:84772589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2047G>A |
| AA Mutation | p.Val683Met(p.V683M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219473 |
| Start | 84745237:84745237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.756G>T |
| AA Mutation | p.Gln252His(p.Q252H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000219473 |
| Start | 84764237:84764237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1806C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000219473 |
| Start | 84744751:84744751(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.270T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000219473 |
| Start | 84778944:84778944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs572473991 |
| CDS Mutation | c.2259C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000219473 |
| Start | 84745360:84745360(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.881delG |
| AA Mutation | p.Gly294ValfsTer17(p.G294Vfs*17) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000219473 |
| Start | 84744938:84744938(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.461delA |
| AA Mutation | p.Lys154SerfsTer10(p.K154Sfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000219473 |
| Start | 84772568:84772569(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2031dupA |
| AA Mutation | p.Leu678ThrfsTer15(p.L678Tfs*15) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |