| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.16133226C>G | CA338624085 | EPHA2 | c.2007G>C (p.Gln669His) n.225G>C c.1845G>C (p.Gln615His) | dbSNP |
| 1 | g.16133226C>A | CA235737 | EPHA2 | c.2007G>T (p.Gln669His) n.225G>T c.1845G>T (p.Gln615His) | ClinVar dbSNP |
| 1 | g.16133226C= | CA1155652412 | EPHA2 | c.2007G= (p.Gln669=) n.225G= c.1845G= (p.Gln615=) | dbSNP |