Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.15069654C>T | CA172752015 | SGCZ | c.39+167931G>A (n.39+167931G>A) c.-90+167931G>A (n.-90+167931G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.15069654C= | CA1766199738 | SGCZ | c.39+167931G= (n.39+167931G=) c.-90+167931G= (n.-90+167931G=) | dbSNP |