Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.126134582T>C | CA1943159723 | ADAM12 | c.416+1002A>G (n.416+1002A>G) c.425+1002A>G (n.425+1002A>G) c.-44+1002A>G (n.-44+1002A>G) | dbSNP |
10 | g.126134582T>G | CA13173775 | ADAM12 | c.416+1002A>C (n.416+1002A>C) c.425+1002A>C (n.425+1002A>C) c.-44+1002A>C (n.-44+1002A>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |