Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.79916743G>C | CA117148 | ELOVL4 | c.810C>G (p.Tyr270Ter) | ClinVar dbSNP |
6 | g.79916743G>A | CA451121009 | ELOVL4 | c.810C>T (p.Tyr270=) | ClinVar dbSNP |
6 | g.79916743G= | CA1640822828 | ELOVL4 | c.810C= (p.Tyr270=) | dbSNP |