Primary Site >> Stomach Cancer
Gene >> EXOSC10
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000376936 |
| Start | 11082689:11082689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1279C>T |
| AA Mutation | p.Arg427Cys(p.R427C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376936 |
| Start | 11087525:11087525(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1012T>G |
| AA Mutation | p.Phe338Val(p.F338V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376936 |
| Start | 11081228:11081228(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764219569 |
| CDS Mutation | c.1291G>A |
| AA Mutation | p.Glu431Lys(p.E431K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376936 |
| Start | 11072116:11072116(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2213C>T |
| AA Mutation | p.Ala738Val(p.A738V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376936 |
| Start | 11091552:11091552(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.418C>T |
| AA Mutation | p.Pro140Ser(p.P140S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376936 |
| Start | 11080890:11080890(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748350072 |
| CDS Mutation | c.1460C>T |
| AA Mutation | p.Thr487Met(p.T487M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376936 |
| Start | 11080799:11080799(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1551G>T |
| AA Mutation | p.Arg517Ser(p.R517S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376936 |
| Start | 11070968:11070968(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201491928 |
| CDS Mutation | c.2248C>T |
| AA Mutation | p.Arg750Trp(p.R750W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376936 |
| Start | 11082739:11082739(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1229A>G |
| AA Mutation | p.Tyr410Cys(p.Y410C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000376936 |
| Start | 11077616:11077616(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775854617 |
| CDS Mutation | c.1785G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000376936 |
| Start | 11069608:11069609(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2438_2439delAA |
| AA Mutation | p.Lys813ArgfsTer28(p.K813Rfs*28) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000376936 |
| Start | 11068063:11068063(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2572delA |
| AA Mutation | p.Ile858LeufsTer?(p.I858Lfs*?) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000376936 |
| Start | 11074273:11074273(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2040delA |
| AA Mutation | p.Ala681ProfsTer93(p.A681Pfs*93) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000376936 |
| Start | 11081080:11081080(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769651237 |
| CDS Mutation | c.1437+2T>C |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |