| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 6 | g.29943445C>T | CA3693382 | HLA-A | c.521C>T (p.Ala174Val) n.797C>T c.437C>T (p.Ala146Val) n.762C>T n.764C>T n.338C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 6 | g.29943445C>G | CA363291598 | HLA-A | c.521C>G (p.Ala174Gly) n.797C>G c.437C>G (p.Ala146Gly) n.762C>G n.764C>G n.338C>G | dbSNP gnomAD v3 gnomAD v4 |
| 6 | g.29943445C>A | CA363291597 | HLA-A | c.521C>A (p.Ala174Asp) n.797C>A c.437C>A (p.Ala146Asp) n.762C>A n.764C>A n.338C>A | dbSNP gnomAD v3 gnomAD v4 |
| 6 | g.29943445C= | CA1618525751 | HLA-A | c.521C= (p.Ala174=) n.797C= c.437C= (p.Ala146=) n.762C= n.764C= n.338C= | dbSNP |