| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.102954362T>G | CA13573756 | MMP13 | c.512-81A>C (n.512-81A>C) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.102954362T>C | CA1996314849 | MMP13 | c.512-81A>G (n.512-81A>G) | dbSNP |
| 11 | g.102954362T= | CA1996314848 | MMP13 | c.512-81A= (n.512-81A=) | dbSNP |