| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.19797472T>A | CA398720663 | ULK2 | c.1733A>T (p.His578Leu) c.1379A>T (p.His460Leu) n.2067A>T c.1796A>T (p.His599Leu) c.956A>T (p.His319Leu) n.2276A>T | dbSNP |
| 17 | g.19797472T>C | CA16609538 | ULK2 | c.1733A>G (p.His578Arg) c.1379A>G (p.His460Arg) n.2067A>G c.1796A>G (p.His599Arg) c.956A>G (p.His319Arg) n.2276A>G | ClinVar dbSNP gnomAD v4 |