Primary Site >> Esophagus Cancer
Gene >> AKAP6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280979 |
| Start | 32822695:32822695(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4882C>G |
| AA Mutation | p.Leu1628Val(p.L1628V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280979 |
| Start | 32823889:32823889(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200684416 |
| CDS Mutation | c.6076G>A |
| AA Mutation | p.Gly2026Arg(p.G2026R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280979 |
| Start | 32545233:32545233(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757619323 |
| CDS Mutation | c.580C>T |
| AA Mutation | p.Arg194Trp(p.R194W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280979 |
| Start | 32822475:32822475(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4662G>C |
| AA Mutation | p.Gln1554His(p.Q1554H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000280979 |
| Start | 32823927:32823927(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6114T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000280979 |
| Start | 32824125:32824125(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6312G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |