| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.102952117G>T | CA120436 | MMP13 | c.694C>A (p.His232Asn) | ClinVar dbSNP |
| 11 | g.102952117G>C | CA382229289 | MMP13 | c.694C>G (p.His232Asp) | dbSNP gnomAD v3 gnomAD v4 |
| 11 | g.102952117G= | CA1996313953 | MMP13 | c.694C= (p.His232=) | dbSNP |
| 11 | g.102952117G>A | CA382229291 | MMP13 | c.694C>T (p.His232Tyr) | dbSNP gnomAD v4 |