| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 20 | g.46010332A>T | CA2366478223 | MMP9 | c.372-151A>T (n.372-151A>T) | dbSNP |
| 20 | g.46010332A>C | CA315634356 | MMP9 | c.372-151A>C (n.372-151A>C) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 20 | g.46010332A= | CA2366478222 | MMP9 | c.372-151A= (n.372-151A=) | dbSNP dbSNP |