Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.169542872G>A | CA10608192 | F5 | c.2218C>T (p.Arg740Ter) c.2233C>T (p.Arg745Ter) c.1807C>T (p.Arg603Ter) | ClinVar dbSNP gnomAD v4 |
1 | g.169542872G>T | CA1234130 | F5 | c.2218C>A (p.Arg740=) c.2233C>A (p.Arg745=) c.1807C>A (p.Arg603=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |