Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.73490480C>T | CA160068957 | BAZ1B | c.694-1089G>A (n.694-1089G>A) n.812-1089G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.73490480C>G | CA1717070067 | BAZ1B | c.694-1089G>C (n.694-1089G>C) n.812-1089G>C | dbSNP |