| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 6 | g.30490287G>T | CA363077670 | HLA-E | c.382G>T (p.Gly128Trp) n.648G>T n.532G>T c.505G>T (p.Gly169Trp) | dbSNP gnomAD v3 gnomAD v4 |
| 6 | g.30490287G>A | CA3697298 | HLA-E | c.382G>A (p.Gly128Arg) n.648G>A n.532G>A c.505G>A (p.Gly169Arg) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 6 | g.30490287G>C | CA363077671 | HLA-E | c.382G>C (p.Gly128Arg) n.648G>C n.532G>C c.505G>C (p.Gly169Arg) | dbSNP |
| 6 | g.30490287G= | CA1618747880 | HLA-E | c.382G= (p.Gly128=) n.648G= n.532G= c.505G= (p.Gly169=) | dbSNP |