Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.77615442G>A | CA7677964 | LINGO1 | c.465C>T (p.Ile155=) c.480C>T (p.Ile160=) c.447C>T (p.Ile149=) n.690-14843G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.77615442G>C | CA393537461 | LINGO1 | c.465C>G (p.Ile155Met) c.480C>G (p.Ile160Met) c.447C>G (p.Ile149Met) n.690-14843G>C | dbSNP |