| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 6 | g.79921660C>T | CA16605161 | ELOVL4 | c.506G>A (p.Trp169Ter) | ClinVar dbSNP |
| 6 | g.79921660C= | CA1640824966 | ELOVL4 | c.506G= (p.Trp169=) | dbSNP |
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 6 | g.79921660C>T | CA16605161 | ELOVL4 | c.506G>A (p.Trp169Ter) | ClinVar dbSNP |
| 6 | g.79921660C= | CA1640824966 | ELOVL4 | c.506G= (p.Trp169=) | dbSNP |