Primary Site >> Liver Cancer
Gene >> DUOX2
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000603300 |
| Start | 45101205:45101205(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778216481 |
| CDS Mutation | c.2921G>A |
| AA Mutation | p.Arg974His(p.R974H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000603300 |
| Start | 45111949:45111949(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.332A>G |
| AA Mutation | p.His111Arg(p.H111R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000603300 |
| Start | 45095582:45095582(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4094G>A |
| AA Mutation | p.Gly1365Glu(p.G1365E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000603300 |
| Start | 45096046:45096046(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3862C>A |
| AA Mutation | p.Gln1288Lys(p.Q1288K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000603300 |
| Start | 45099462:45099462(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757212555 |
| CDS Mutation | c.3436G>A |
| AA Mutation | p.Ala1146Thr(p.A1146T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000603300 |
| Start | 45104016:45104016(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2598G>A |
| AA Mutation | p.Met866Ile(p.M866I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000603300 |
| Start | 45094975:45094975(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4356C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000603300 |
| Start | 45108057:45108059(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1562_1564delACA |
| AA Mutation | p.Asn521del(p.N521del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |