Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.89023563C>A | CA1926643639 | FAS | c.*9113C>A (n.*9113C>A) | dbSNP |
10 | g.89023563C>T | CA15652760 | FAS | c.*9113C>T (n.*9113C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.89023563C= | CA1926643638 | FAS | c.*9113C= (n.*9113C=) | dbSNP |