Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.169567201C>T | CA32401502 | F5 | c.373+5020G>A (n.373+5020G>A) c.-39+5020G>A (n.-39+5020G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.169567201C>G | CA1206145100 | F5 | c.373+5020G>C (n.373+5020G>C) c.-39+5020G>C (n.-39+5020G>C) | dbSNP |