| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.16129440G>A | CA122981 | EPHA2 | c.2819C>T (p.Thr940Ile) c.2657C>T (p.Thr886Ile) | ClinVar dbSNP |
| 1 | g.16129440G>C | CA338615228 | EPHA2 | c.2819C>G (p.Thr940Ser) c.2657C>G (p.Thr886Ser) | dbSNP |
| 1 | g.16129440G= | CA1141580614 | EPHA2 | c.2819C= (p.Thr940=) c.2657C= (p.Thr886=) | dbSNP |