| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.77615433T>A | CA491507667 | LINGO1 | c.474A>T (p.Leu158=) c.489A>T (p.Leu163=) c.456A>T (p.Leu152=) n.690-14852T>A | dbSNP |
| 15 | g.77615433T>C | CA7677962 | LINGO1 | c.474A>G (p.Leu158=) c.489A>G (p.Leu163=) c.456A>G (p.Leu152=) n.690-14852T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |