| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.94531732G>A | CA10680610 | F3 | c.751+589C>T (n.751+589C>T) c.592-1136C>T (n.592-1136C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.94531732G>C | CA1181620241 | F3 | c.751+589C>G (n.751+589C>G) c.592-1136C>G (n.592-1136C>G) | dbSNP |