| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.134887245G>C | CA5321362 | FCN2 | c.772G>C (p.Ala258Pro) c.658G>C (p.Ala220Pro) c.625G>C (p.Ala209Pro) c.739G>C (p.Ala247Pro) | dbSNP ExAC |
| 9 | g.134887245G>T | CA5321361 | FCN2 | c.772G>T (p.Ala258Ser) c.658G>T (p.Ala220Ser) c.625G>T (p.Ala209Ser) c.739G>T (p.Ala247Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |