Primary Site >> Esophagus Cancer
Gene >> EML4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318522 |
| Start | 42329981:42329981(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2720A>G |
| AA Mutation | p.Asn907Ser(p.N907S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318522 |
| Start | 42329891:42329891(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756245593 |
| CDS Mutation | c.2630C>T |
| AA Mutation | p.Ala877Val(p.A877V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318522 |
| Start | 42280951:42280951(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.769G>C |
| AA Mutation | p.Glu257Gln(p.E257Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318522 |
| Start | 42280889:42280889(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.707T>A |
| AA Mutation | p.Ile236Asn(p.I236N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000318522 |
| Start | 42263298:42263298(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.633T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000318522 |
| Start | 42284685:42284685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs566921568 |
| CDS Mutation | c.993C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |