| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 20 | g.63493155C>G | CA200125 | EEF1A2 | c.754G>C (p.Asp252His) n.3323G>C c.*626G>C (n.*626G>C) | ClinVar dbSNP |
| 20 | g.63493155C>T | CA409648631 | EEF1A2 | c.754G>A (p.Asp252Asn) n.3323G>A c.*626G>A (n.*626G>A) | ClinVar dbSNP |
| 20 | g.63493155C= | CA2374822823 | EEF1A2 | c.754G= (p.Asp252=) n.3323G= c.*626G= (n.*626G=) | dbSNP |