Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
21 | g.38823912C>G | CA15982001 | ETS2 | c.*1023C>G (n.*1023C>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
21 | g.38823912C>T | CA637810352 | ETS2 | c.*1023C>T (n.*1023C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
21 | g.38823912C= | CA2389091585 | ETS2 | c.*1023C= (n.*1023C=) | dbSNP |