Primary Site >> Stomach Cancer
Gene >> DCAF6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312263 |
| Start | 167951808:167951808(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.106G>A |
| AA Mutation | p.Glu36Lys(p.E36K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312263 |
| Start | 168068368:168068368(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766445617 |
| CDS Mutation | c.2423G>A |
| AA Mutation | p.Arg808Gln(p.R808Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312263 |
| Start | 167974870:167974870(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.293T>C |
| AA Mutation | p.Phe98Ser(p.F98S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312263 |
| Start | 168002564:168002564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.986G>A |
| AA Mutation | p.Arg329Gln(p.R329Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312263 |
| Start | 168002486:168002486(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.908G>A |
| AA Mutation | p.Arg303Gln(p.R303Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312263 |
| Start | 167987535:167987535(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.479G>C |
| AA Mutation | p.Cys160Ser(p.C160S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000312263 |
| Start | 167993300:167993300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.763A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000312263 |
| Start | 168004780:168004780(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1365A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000312263 |
| Start | 167993373:167993373(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.840delT |
| AA Mutation | p.Phe280LeufsTer31(p.F280Lfs*31) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000312263 |
| Start | 168002485:168002485(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs184187462 |
| CDS Mutation | c.907C>T |
| AA Mutation | p.Arg303Ter(p.R303*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |