Primary Site >> Esophagus Cancer
Gene >> CASZ1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377022 |
| Start | 10665094:10665094(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.494G>T |
| AA Mutation | p.Arg165Met(p.R165M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377022 |
| Start | 10648084:10648084(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3214C>T |
| AA Mutation | p.Pro1072Ser(p.P1072S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377022 |
| Start | 10665159:10665159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749040511 |
| CDS Mutation | c.429C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377022 |
| Start | 10655685:10655685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1629C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377022 |
| Start | 10655694:10655694(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs575650869 |
| CDS Mutation | c.1620C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377022 |
| Start | 10649090:10649090(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3138C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |