| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.94761900C>T | CA10602359 | c.932-13158C>T (n.932-13158C>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 | |
| 10 | g.94761900C>A | CA10576167 | c.932-13158C>A (n.932-13158C>A) | dbSNP | |
| 10 | g.94761900C= | CA1929212681 | c.932-13158C= (n.932-13158C=) | dbSNP |