Primary Site >> Esophagus Cancer
Gene >> FASN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306749 |
| Start | 82079253:82079253(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs1140623 |
| CDS Mutation | c.7426G>A |
| AA Mutation | p.Val2476Ile(p.V2476I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306749 |
| Start | 82084528:82084528(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765330213 |
| CDS Mutation | c.4753C>T |
| AA Mutation | p.Pro1585Ser(p.P1585S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306749 |
| Start | 82088207:82088207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373471307 |
| CDS Mutation | c.2694G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306749 |
| Start | 82085638:82085638(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765948097 |
| CDS Mutation | c.3966C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306749 |
| Start | 82088406:82088406(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778504673 |
| CDS Mutation | c.2577C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306749 |
| Start | 82080547:82080547(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6870C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306749 |
| Start | 82083304:82083304(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5463G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | splice_acceptor_variant;coding_sequence_variant;intron_variant |
| Transcription ID | ENST00000306749 |
| Start | 82091032:82091090(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1493-21_1530delGTGACGTGCTCTCTGGGACAGGGATGGGCACACAGTGGCGCGGGATGGGGCTGAGCCTC |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |