| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.101231117G>A | CA270121 | IMPG2 | c.3262C>T (p.Arg1088Ter) c.2968C>T (p.Arg990Ter) c.2851C>T (p.Arg951Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 3 | g.101231117G= | CA1388606745 | IMPG2 | c.3262C= (p.Arg1088=) c.2968C= (p.Arg990=) c.2851C= (p.Arg951=) | dbSNP |