Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
20 | g.46011586A>C | CA409214474 | MMP9 | c.836A>C (p.Gln279Pro) | dbSNP |
20 | g.46011586A>G | CA9886546 | MMP9 | c.836A>G (p.Gln279Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
20 | g.46011586A>T | CA409214480 | MMP9 | c.836A>T (p.Gln279Leu) | dbSNP |
20 | g.46011586A= | CA2366478856 | MMP9 | c.836A= (p.Gln279=) | dbSNP |