| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 18 | g.62361793G>A | CA402614439 | TNFRSF11A | c.730G>A (p.Ala244Thr) c.616+1744G>A (n.616+1744G>A) c.730G>A (p.Gly244Arg) c.688G>A (p.Ala230Thr) c.745G>A (p.Ala249Thr) c.622G>A (p.Ala208Thr) n.760G>A c.580G>A (p.Ala194Thr) c.520G>A (p.Ala174Thr) | dbSNP |
| 18 | g.62361793G>T | CA118118 | TNFRSF11A | c.730G>T (p.Ala244Ser) c.616+1744G>T (n.616+1744G>T) c.730G>T (p.Gly244Ter) c.688G>T (p.Ala230Ser) c.745G>T (p.Ala249Ser) c.622G>T (p.Ala208Ser) n.760G>T c.580G>T (p.Ala194Ser) c.520G>T (p.Ala174Ser) | ClinVar dbSNP |