Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.97507492C>T | CA2057176521 | RMST | n.803+11436C>T n.804+11436C>T n.915+11436C>T | dbSNP |
12 | g.97507492C>A | CA242581073 | RMST | n.803+11436C>A n.804+11436C>A n.915+11436C>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |