Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.68413742C>T | CA118087 | LRP5 | c.2557C>T (p.Gln853Ter) c.*1163C>T (n.*1163C>T) c.814C>T (p.Gln272Ter) c.2584C>T (p.Gln862Ter) n.2599C>T c.97C>T (p.Gln33Ter) n.2823C>T | ClinVar dbSNP |
11 | g.68413742C= | CA1980597936 | LRP5 | c.2557C= (p.Gln853=) c.*1163C= (n.*1163C=) c.814C= (p.Gln272=) c.2584C= (p.Gln862=) n.2599C= c.97C= (p.Gln33=) n.2823C= | dbSNP |