Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.171107795G>A | CA1240538 | FMO3 | c.442G>A (p.Gly148Arg) c.253G>A (p.Gly85Arg) c.382G>A (p.Gly128Arg) c.-106G>A (n.-106G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.171107795G>T | CA126357 | FMO3 | c.442G>T (p.Gly148Ter) c.253G>T (p.Gly85Ter) c.382G>T (p.Gly128Ter) c.-106G>T (n.-106G>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |