| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.65404419C>T | CA16603113 | EPHA5 | c.1748G>A (p.Gly583Glu) c.1745G>A (p.Gly582Glu) c.1256G>A (p.Gly419Glu) c.1541G>A (p.Gly514Glu) c.1412G>A (p.Gly471Glu) c.1409G>A (p.Gly470Glu) c.1253G>A (p.Gly418Glu) | ClinVar dbSNP COSMIC |
| 4 | g.65404419C>G | CA357052956 | EPHA5 | c.1748G>C (p.Gly583Ala) c.1745G>C (p.Gly582Ala) c.1256G>C (p.Gly419Ala) c.1541G>C (p.Gly514Ala) c.1412G>C (p.Gly471Ala) c.1409G>C (p.Gly470Ala) c.1253G>C (p.Gly418Ala) | dbSNP |