Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.171108154T>G | CA1240575 | FMO3 | c.560T>G (p.Val187Gly) c.506T>G (p.Val169Gly) c.371T>G (p.Val124Gly) c.500T>G (p.Val167Gly) c.13T>G (p.Ser5Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.171108154T>C | CA356599 | FMO3 | c.560T>C (p.Val187Ala) c.506T>C (p.Val169Ala) c.371T>C (p.Val124Ala) c.500T>C (p.Val167Ala) c.13T>C (p.Ser5Pro) | dbSNP |