Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.79516830C>A | CA14270067 | MAF | c.*28+69050G>T (n.*28+69050G>T) n.3230+69050G>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.79516830C>G | CA2235890128 | MAF | c.*28+69050G>C (n.*28+69050G>C) n.3230+69050G>C | dbSNP |
16 | g.79516830C>T | CA724420016 | MAF | c.*28+69050G>A (n.*28+69050G>A) n.3230+69050G>A | dbSNP |