Primary Site >> Esophagus Cancer
Gene >> FLT3
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000241453 |
| Start | 28062068:28062068(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.167T>C |
| AA Mutation | p.Val56Ala(p.V56A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241453 |
| Start | 28033929:28033929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1900A>G |
| AA Mutation | p.Lys634Glu(p.K634E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241453 |
| Start | 28048288:28048288(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1192G>A |
| AA Mutation | p.Asp398Asn(p.D398N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241453 |
| Start | 28049718:28049718(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.799C>A |
| AA Mutation | p.Pro267Thr(p.P267T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241453 |
| Start | 28049441:28049441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.979T>C |
| AA Mutation | p.Tyr327His(p.Y327H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000241453 |
| Start | 28052595:28052595(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774682624 |
| CDS Mutation | c.564C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000241453 |
| Start | 28049464:28049464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.956C>A |
| AA Mutation | p.Ser319Ter(p.S319*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000241453 |
| Start | 28049538:28049538(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.883-1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |