Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.67586499T>C | CA6142903 | GSTP1 | c.447T>C (p.Ser149=) c.555T>C (p.Ser185=) c.*271T>C (n.*271T>C) n.666T>C n.1527T>C c.618T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.67586499T= | CA1980216539 | GSTP1 | c.447T= (p.Ser149=) c.555T= (p.Ser185=) c.*271T= (n.*271T=) n.666T= n.1527T= c.618T= | dbSNP |