| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 6 | g.79921662C>G | CA170078 | ELOVL4 | c.504G>C (p.Leu168Phe) | ClinVar dbSNP |
| 6 | g.79921662C>T | CA142271129 | ELOVL4 | c.504G>A (p.Leu168=) | dbSNP gnomAD v4 |
| 6 | g.79921662C= | CA1640824967 | ELOVL4 | c.504G= (p.Leu168=) | dbSNP |