Primary Site >> Esophagus Cancer
Gene >> FAT1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000441802 |
| Start | 186707070:186707070(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2758G>A |
| AA Mutation | p.Val920Ile(p.V920I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000441802 |
| Start | 186619920:186619920(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6666C>G |
| AA Mutation | p.Asp2222Glu(p.D2222E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000441802 |
| Start | 186619901:186619901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759239082 |
| CDS Mutation | c.6685A>G |
| AA Mutation | p.Ile2229Val(p.I2229V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000441802 |
| Start | 186619191:186619191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7395G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000441802 |
| Start | 186603690:186603690(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10836C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000441802 |
| Start | 186707965:186707965(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs551785621 |
| CDS Mutation | c.1863G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000441802 |
| Start | 186707942:186707942(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1886delC |
| AA Mutation | p.Ser629CysfsTer2(p.S629Cfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000441802 |
| Start | 186617118:186617118(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8962A>T |
| AA Mutation | p.Lys2988Ter(p.K2988*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000441802 |
| Start | 186620389:186620391(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.6195_6197delTGT |
| AA Mutation | p.Val2067del(p.V2067del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |