Primary Site >> Esophagus Cancer
Gene >> CTNND1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399050 |
| Start | 57808406:57808406(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2108G>T |
| AA Mutation | p.Arg703Leu(p.R703L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399050 |
| Start | 57815936:57815936(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2830C>G |
| AA Mutation | p.Leu944Val(p.L944V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000399050 |
| Start | 57796842:57796842(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.806G>C |
| AA Mutation | p.Ser269Thr(p.S269T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000399050 |
| Start | 57808536:57808536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2238A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000399050 |
| Start | 57808538:57808538(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2241delT |
| AA Mutation | p.Ile747MetfsTer10(p.I747Mfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000399050 |
| Start | 57796958:57796958(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.922delA |
| AA Mutation | p.Thr308LeufsTer17(p.T308Lfs*17) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000399050 |
| Start | 57809420:57809420(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2389C>T |
| AA Mutation | p.Arg797Ter(p.R797*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000399050 |
| Start | 57808266:57808266(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2065C>T |
| AA Mutation | p.Gln689Ter(p.Q689*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |