Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.31356226T>G | CA3711521 | HLA-B | n.2033A>C c.560A>C (p.Glu187Ala) c.593A>C (p.Glu198Ala) n.435A>C n.826A>C n.570A>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
6 | g.31356226T>C | CA3711522 | HLA-B | n.2033A>G c.560A>G (p.Glu187Gly) c.593A>G (p.Glu198Gly) n.435A>G n.826A>G n.570A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.31356226T>A | CA3711520 | HLA-B | n.2033A>T c.560A>T (p.Glu187Val) c.593A>T (p.Glu198Val) n.435A>T n.826A>T n.570A>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |