Primary Site >> Liver Cancer
Gene >> DUOX1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321429 |
| Start | 45145010:45145010(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2252T>A |
| AA Mutation | p.Met751Lys(p.M751K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321429 |
| Start | 45135510:45135510(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.532A>G |
| AA Mutation | p.Ile178Val(p.I178V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321429 |
| Start | 45148298:45148298(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2669G>C |
| AA Mutation | p.Cys890Ser(p.C890S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321429 |
| Start | 45144922:45144922(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772812512 |
| CDS Mutation | c.2164C>T |
| AA Mutation | p.Arg722Trp(p.R722W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321429 |
| Start | 45134296:45134296(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.294G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321429 |
| Start | 45140936:45140936(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1431C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321429 |
| Start | 45151219:45151219(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2985C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |