| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 21 | g.45504431C>T | CA236429 | COL18A1,SLC19A1 | c.3283C>T (p.Arg1095Ter) c.2743C>T (p.Arg915Ter) c.784C>T (p.Arg262Ter) c.3988C>T (p.Arg1330Ter) c.498-5819G>A c.1294-5819G>A (n.1294-5819G>A) c.1585-1462G>A (n.1585-1462G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 21 | g.45504431C= | CA2392190666 | COL18A1,SLC19A1 | c.3283C= (p.Arg1095=) c.2743C= (p.Arg915=) c.784C= (p.Arg262=) c.3988C= (p.Arg1330=) c.498-5819G= c.1294-5819G= (n.1294-5819G=) c.1585-1462G= (n.1585-1462G=) | dbSNP |