Primary Site >> Esophagus Cancer
Gene >> CTNND2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 11082818:11082818(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2666G>T |
| AA Mutation | p.Arg889Leu(p.R889L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 11022908:11022908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2860G>T |
| AA Mutation | p.Ala954Ser(p.A954S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304623 |
| Start | 11384738:11384738(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1104G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304623 |
| Start | 11411636:11411636(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374819899 |
| CDS Mutation | c.339C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304623 |
| Start | 11732208:11732208(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.102C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000304623 |
| Start | 10973468:10973468(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3663delC |
| AA Mutation | p.Asp1222ThrfsTer38(p.D1222Tfs*38) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |