Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.122077513C>A | CA360876052 | LOX | c.473G>T (p.Arg158Leu) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
5 | g.122077513C>T | CA123899 | LOX | c.473G>A (p.Arg158Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.122077513C>G | CA360876054 | LOX | c.473G>C (p.Arg158Pro) | dbSNP |
5 | g.122077513C= | CA1578379563 | LOX | c.473G= (p.Arg158=) | dbSNP |