| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.104703343T>C | CA114722 | INF2 | c.556T>C (p.Ser186Pro) c.440T>C (p.Leu147Pro) c.545T>C (p.Leu182Pro) n.758T>C c.652T>C (p.Ser218Pro) n.781T>C n.757T>C | ClinVar dbSNP |
| 14 | g.104703343T= | CA2160925625 | INF2 | c.556T= (p.Ser186=) c.440T= (p.Leu147=) c.545T= (p.Leu182=) n.758T= c.652T= (p.Ser218=) n.781T= n.757T= | dbSNP |