Primary Site >> Esophagus Cancer
Gene >> ATP2C1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000428331 |
| Start | 130953866:130953866(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.577A>C |
| AA Mutation | p.Thr193Pro(p.T193P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000428331 |
| Start | 130997715:130997715(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2353A>G |
| AA Mutation | p.Ile785Val(p.I785V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000428331 |
| Start | 130996682:130996682(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2129G>C |
| AA Mutation | p.Ser710Thr(p.S710T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000428331 |
| Start | 130953891:130953891(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.602C>T |
| AA Mutation | p.Pro201Leu(p.P201L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000428331 |
| Start | 130975477:130975477(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779717457 |
| CDS Mutation | c.1559C>T |
| AA Mutation | p.Ala520Val(p.A520V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000428331 |
| Start | 130964990:130964990(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1067C>A |
| AA Mutation | p.Thr356Lys(p.T356K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000428331 |
| Start | 130940647:130940647(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.378A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |