| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.21564097G>A | CA666521 | ALPL | c.529G>A (p.Ala177Thr) n.589G>A c.298G>A (p.Ala100Thr) c.364G>A (p.Ala122Thr) c.373G>A (p.Ala125Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.21564097G= | CA1143366459 | ALPL | c.529G= (p.Ala177=) n.589G= c.298G= (p.Ala100=) c.364G= (p.Ala122=) c.373G= (p.Ala125=) | dbSNP |
| 1 | g.21564097G>T | CA338877902 | ALPL | c.529G>T (p.Ala177Ser) n.589G>T c.298G>T (p.Ala100Ser) c.364G>T (p.Ala122Ser) c.373G>T (p.Ala125Ser) | ClinVar dbSNP gnomAD v4 COSMIC |