Primary Site >> Esophagus Cancer
Gene >> CD163
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359156 |
| Start | 7487881:7487881(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1627G>A |
| AA Mutation | p.Glu543Lys(p.E543K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359156 |
| Start | 7485139:7485139(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2736G>C |
| AA Mutation | p.Lys912Asn(p.K912N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000359156 |
| Start | 7497133:7497133(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.779A>G |
| AA Mutation | p.Lys260Arg(p.K260R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359156 |
| Start | 7482694:7482694(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139478533 |
| CDS Mutation | c.3196G>A |
| AA Mutation | p.Val1066Ile(p.V1066I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359156 |
| Start | 7502488:7502488(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.123C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000359156 |
| Start | 7482696:7482696(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3194delT |
| AA Mutation | p.Phe1065SerfsTer7(p.F1065Sfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |