Primary Site >> Liver Cancer
Gene >> FAT1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000441802 |
| Start | 186707702:186707702(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2126T>C |
| AA Mutation | p.Val709Ala(p.V709A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000441802 |
| Start | 186603179:186603179(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11347A>C |
| AA Mutation | p.Lys3783Gln(p.K3783Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000441802 |
| Start | 186588963:186588963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758477097 |
| CDS Mutation | c.13396A>G |
| AA Mutation | p.Arg4466Gly(p.R4466G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000441802 |
| Start | 186709558:186709558(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373265178 |
| CDS Mutation | c.270C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000441802 |
| Start | 186617140:186617140(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8940G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000441802 |
| Start | 186618072:186618072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8514A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000441802 |
| Start | 186636170:186636170(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4038C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000441802 |
| Start | 186617940:186617940(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767714665 |
| CDS Mutation | c.8646T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000441802 |
| Start | 186620358:186620358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6228T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000441802 |
| Start | 186613224:186613224(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.9348delA |
| AA Mutation | p.Asp3117MetfsTer2(p.D3117Mfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000441802 |
| Start | 186709821:186709821(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7A>T |
| AA Mutation | p.Arg3Ter(p.R3*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | stop_gained;splice_region_variant |
| Transcription ID | ENST00000441802 |
| Start | 186606072:186606072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10348C>T |
| AA Mutation | p.Gln3450Ter(p.Q3450*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | stop_lost |
| Transcription ID | ENST00000441802 |
| Start | 186588593:186588593(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.13766G>T |
| AA Mutation | p.Ter4589LeuextTer94(p.*4589Lext*94) |
| Mutation Classification | Nonstop_Mutation |
| Feature Type | Transcript |