Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.31356195C>A | CA3711502 | HLA-B | n.2064G>T c.591G>T (p.Glu197Asp) c.624G>T (p.Glu208Asp) n.466G>T n.857G>T n.601G>T | dbSNP ExAC gnomAD v3 gnomAD v4 |
6 | g.31356195C>T | CA136833618 | HLA-B | n.2064G>A c.591G>A (p.Glu197=) c.624G>A (p.Glu208=) n.466G>A n.857G>A n.601G>A | dbSNP gnomAD v4 |