Primary Site >> Esophagus Cancer
Gene >> ITGAX
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268296 |
| Start | 31380927:31380927(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3307C>G |
| AA Mutation | p.His1103Asp(p.H1103D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268296 |
| Start | 31357316:31357316(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.382C>T |
| AA Mutation | p.Leu128Phe(p.L128F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268296 |
| Start | 31362630:31362630(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1236C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268296 |
| Start | 31379631:31379631(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2853C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268296 |
| Start | 31363233:31363233(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144979651 |
| CDS Mutation | c.1569G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268296 |
| Start | 31379831:31379831(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2943T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |