| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.4379476C>T | CA16619523 | FGF23 | c.107G>A (p.Trp36Ter) c.*1967+13194C>T (n.*1967+13194C>T) c.*1204+13194C>T (n.*1204+13194C>T) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 12 | g.4379476C= | CA2013135050 | FGF23 | c.107G= (p.Trp36=) c.*1967+13194C= (n.*1967+13194C=) c.*1204+13194C= (n.*1204+13194C=) | dbSNP |