| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.113149146C>T | CA121837 | F10 | c.1096C>T (p.Arg366Cys) c.*87C>T (n.*87C>T) c.964C>T (p.Arg322Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.113149146C>G | CA388793026 | F10 | c.1096C>G (p.Arg366Gly) c.*87C>G (n.*87C>G) c.964C>G (p.Arg322Gly) | dbSNP gnomAD v3 gnomAD v4 |