Primary Site >> Liver Cancer
Gene >> DNAH17
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389840 |
| Start | 78450719:78450719(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10862A>T |
| AA Mutation | p.Glu3621Val(p.E3621V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389840 |
| Start | 78571351:78571351(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.760G>A |
| AA Mutation | p.Val254Ile(p.V254I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389840 |
| Start | 78484965:78484965(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7552G>C |
| AA Mutation | p.Val2518Leu(p.V2518L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389840 |
| Start | 78505393:78505393(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61745476 |
| CDS Mutation | c.4856G>A |
| AA Mutation | p.Arg1619Gln(p.R1619Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389840 |
| Start | 78437754:78437754(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11920C>A |
| AA Mutation | p.Pro3974Thr(p.P3974T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389840 |
| Start | 78425526:78425526(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12961T>A |
| AA Mutation | p.Trp4321Arg(p.W4321R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389840 |
| Start | 78507506:78507506(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4536G>C |
| AA Mutation | p.Gln1512His(p.Q1512H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389840 |
| Start | 78444764:78444764(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11368G>T |
| AA Mutation | p.Asp3790Tyr(p.D3790Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389840 |
| Start | 78507748:78507748(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4294C>A |
| AA Mutation | p.Pro1432Thr(p.P1432T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389840 |
| Start | 78455714:78455714(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10100G>A |
| AA Mutation | p.Gly3367Asp(p.G3367D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389840 |
| Start | 78494739:78494739(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6124G>C |
| AA Mutation | p.Ala2042Pro(p.A2042P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389840 |
| Start | 78449508:78449508(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11117T>A |
| AA Mutation | p.Leu3706Gln(p.L3706Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389840 |
| Start | 78539829:78539829(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2584T>C |
| AA Mutation | p.Tyr862His(p.Y862H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389840 |
| Start | 78460254:78460254(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754934381 |
| CDS Mutation | c.9343G>A |
| AA Mutation | p.Val3115Ile(p.V3115I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389840 |
| Start | 78466778:78466778(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8817G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389840 |
| Start | 78486095:78486095(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs555133387 |
| CDS Mutation | c.7140C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |