Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
18 | g.62354528C>T | CA8983721 | TNFRSF11A | c.421C>T (p.His141Tyr) c.303C>T (p.Ser101=) n.436C>T c.256C>T (p.His86Tyr) c.201C>T (p.Ser67=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.62354528C= | CA2308282849 | TNFRSF11A | c.421C= (p.His141=) c.303C= (p.Ser101=) n.436C= c.256C= (p.His86=) c.201C= (p.Ser67=) | dbSNP |