Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
18 | g.62387624A>C | CA15918156 | TNFRSF11A | c.*2590A>C (n.*2590A>C) c.*2865A>C (n.*2865A>C) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.62387624A>T | CA781276861 | TNFRSF11A | c.*2590A>T (n.*2590A>T) c.*2865A>T (n.*2865A>T) | dbSNP |