Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.206842612T>C | CA1364115 | IL19 | c.524T>C (p.Phe175Ser) c.638T>C (p.Phe213Ser) n.210A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.206842612T>G | CA344486381 | IL19 | c.524T>G (p.Phe175Cys) c.638T>G (p.Phe213Cys) n.210A>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.206842612T= | CA1139923043 | IL19 | c.524T= (p.Phe175=) c.638T= (p.Phe213=) n.210A= | dbSNP |