Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
20 | g.46008928T>A | CA127077 | MMP9 | c.2T>A (p.Met1Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
20 | g.46008928T>C | CA9886297 | MMP9 | c.2T>C (p.Met1Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
20 | g.46008928T>G | CA409209429 | MMP9 | c.2T>G (p.Met1Arg) | dbSNP gnomAD v3 gnomAD v4 |
20 | g.46008928T= | CA2366477573 | MMP9 | c.2T= (p.Met1=) | dbSNP |