Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.46894748T>G | CA117688 | LRP4 | c.1381A>C (p.Thr461Pro) c.1594A>C (p.Thr532Pro) c.577A>C (p.Thr193Pro) | ClinVar dbSNP |
11 | g.46894748T>C | CA380285845 | LRP4 | c.1381A>G (p.Thr461Ala) c.1594A>G (p.Thr532Ala) c.577A>G (p.Thr193Ala) | dbSNP gnomAD v2 gnomAD v4 |
11 | g.46894748T>A | CA380285843 | LRP4 | c.1381A>T (p.Thr461Ser) c.1594A>T (p.Thr532Ser) c.577A>T (p.Thr193Ser) | dbSNP gnomAD v4 |
11 | g.46894748T= | CA1969144893 | LRP4 | c.1381A= (p.Thr461=) c.1594A= (p.Thr532=) c.577A= (p.Thr193=) | dbSNP |