| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.125451587G>A | CA3073706 | FAT4 | c.10577G>A (p.Gly3526Asp) c.5348G>A (p.Gly1783Asp) c.5465G>A (p.Gly1822Asp) c.10571G>A (p.Gly3524Asp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.125451587G>C | CA358159009 | FAT4 | c.10577G>C (p.Gly3526Ala) c.5348G>C (p.Gly1783Ala) c.5465G>C (p.Gly1822Ala) c.10571G>C (p.Gly3524Ala) | dbSNP |