Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.55368743C>T | CA5990339 | OR4A15 | c.770C>T (p.Ala257Val) c.860C>T (p.Ala287Val) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.55368743C= | CA1974344651 | OR4A15 | c.770C= (p.Ala257=) c.860C= (p.Ala287=) | dbSNP |
11 | g.55368743C>A | CA380453923 | OR4A15 | c.770C>A (p.Ala257Glu) c.860C>A (p.Ala287Glu) | dbSNP gnomAD v4 |