| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 18 | g.62360008C>A | CA402613705 | TNFRSF11A | c.575C>A (p.Ala192Glu) n.493C>A c.533C>A (p.Ala178Glu) c.590C>A (p.Ala197Glu) c.467C>A (p.Ala156Glu) n.605C>A c.425C>A (p.Ala142Glu) c.365C>A (p.Ala122Glu) | dbSNP |
| 18 | g.62360008C>T | CA8983802 | TNFRSF11A | c.575C>T (p.Ala192Val) n.493C>T c.533C>T (p.Ala178Val) c.590C>T (p.Ala197Val) c.467C>T (p.Ala156Val) n.605C>T c.425C>T (p.Ala142Val) c.365C>T (p.Ala122Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.62360008C= | CA2308285234 | TNFRSF11A | c.575C= (p.Ala192=) n.493C= c.533C= (p.Ala178=) c.590C= (p.Ala197=) c.467C= (p.Ala156=) n.605C= c.425C= (p.Ala142=) c.365C= (p.Ala122=) | dbSNP |