| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.104703439C>T | CA114724 | INF2 | c.652C>T (p.Arg218Trp) c.536C>T (n.536C>T) c.641C>T (n.641C>T) n.854C>T c.748C>T (p.Arg250Trp) n.877C>T n.853C>T | ClinVar dbSNP |
| 14 | g.104703439C= | CA2160925679 | INF2 | c.652C= (p.Arg218=) c.536C= (n.536C=) c.641C= (n.641C=) n.854C= c.748C= (p.Arg250=) n.877C= n.853C= | dbSNP |