Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.113129630T>C | CA1838798 | IL1RN | c.69T>C (p.Ala23=) c.171T>C (p.Ala57=) c.180T>C (p.Ala60=) c.117T>C (p.Ala39=) n.220T>C n.155T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.113129630T= | CA1280071895 | IL1RN | c.69T= (p.Ala23=) c.171T= (p.Ala57=) c.180T= (p.Ala60=) c.117T= (p.Ala39=) n.220T= n.155T= | dbSNP |