| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 20 | g.46016514T>C | CA10649785 | MMP9,SLC12A5-AS1 | c.*146T>C (n.*146T>C) n.669-1726A>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.46016514T= | CA2366481152 | MMP9,SLC12A5-AS1 | c.*146T= (n.*146T=) n.669-1726A= | dbSNP |