Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.40299125A>G | CA339924 | LRRK2 | c.3364A>G (p.Ile1122Val) c.*2273A>G (n.*2273A>G) c.3109A>G (p.Ile1037Val) c.408A>G n.45A>G c.2161A>G (p.Ile721Val) c.280A>G (p.Ile94Val) n.3606A>G | ClinVar dbSNP gnomAD v4 |
12 | g.40299125A= | CA2030983872 | LRRK2 | c.3364A= (p.Ile1122=) c.*2273A= (n.*2273A=) c.3109A= (p.Ile1037=) c.408A= n.45A= c.2161A= (p.Ile721=) c.280A= (p.Ile94=) n.3606A= | dbSNP |