Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.65965972C>A | CA13623917 | HMGA2 | c.*2680C>A (n.*2680C>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.65965972C>G | CA2042817574 | HMGA2 | c.*2680C>G (n.*2680C>G) | dbSNP |
12 | g.65965972C>T | CA2042817575 | HMGA2 | c.*2680C>T (n.*2680C>T) | dbSNP |