Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.30073033T>G | CA12412394 | RNF39 | c.478+124A>C (n.478+124A>C) c.682+124A>C (n.682+124A>C) c.223+124A>C (n.223+124A>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.30073033T>C | CA1618577341 | RNF39 | c.478+124A>G (n.478+124A>G) c.682+124A>G (n.682+124A>G) c.223+124A>G (n.223+124A>G) | dbSNP |