Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.297184A>G | CA7774063 | AXIN1 | c.1827T>C (p.Ala609=) n.1124T>C c.1989T>C (p.Ala663=) c.1842T>C (p.Ala614=) c.1011T>C (p.Ala337=) c.984T>C (p.Ala328=) c.777T>C (p.Ala259=) n.2119T>C c.1974T>C (p.Ala658=) c.987T>C (p.Ala329=) n.2166T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.297184A>T | CA492795069 | AXIN1 | c.1827T>A (p.Ala609=) n.1124T>A c.1989T>A (p.Ala663=) c.1842T>A (p.Ala614=) c.1011T>A (p.Ala337=) c.984T>A (p.Ala328=) c.777T>A (p.Ala259=) n.2119T>A c.1974T>A (p.Ala658=) c.987T>A (p.Ala329=) n.2166T>A | dbSNP gnomAD v4 |