Primary Site >> Esophagus Cancer
Gene >> ALPK2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361673 |
| Start | 58580297:58580297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.479C>T |
| AA Mutation | p.Ser160Leu(p.S160L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361673 |
| Start | 58579158:58579158(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1618C>T |
| AA Mutation | p.Pro540Ser(p.P540S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361673 |
| Start | 58580472:58580472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752603625 |
| CDS Mutation | c.304G>A |
| AA Mutation | p.Val102Ile(p.V102I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361673 |
| Start | 58536064:58536064(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4123G>C |
| AA Mutation | p.Asp1375His(p.D1375H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361673 |
| Start | 58482034:58482034(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6302A>G |
| AA Mutation | p.Lys2101Arg(p.K2101R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361673 |
| Start | 58535297:58535297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4890T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |