| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.44901113C>T | CA16615444 | CCDC103,FAM187A | c.115C>T (p.Gln39Ter) c.-1627C>T (n.-1627C>T) | ClinVar dbSNP gnomAD v4 |
| 17 | g.44901113C= | CA2261607350 | CCDC103,FAM187A | c.115C= (p.Gln39=) c.-1627C= (n.-1627C=) | dbSNP |