Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.38550324C>T | CA16609848 | SCN5A | c.6045G>A (p.Val2015=) c.6048G>A (p.Val2016=) c.5994G>A (p.Val1998=) c.5886G>A (p.Val1962=) c.5949G>A (p.Val1983=) c.5919G>A (p.Val1973=) c.5991G>A (p.Val1997=) | ClinVar dbSNP |
3 | g.38550324C= | CA1358561697 | SCN5A | c.6045G= (p.Val2015=) c.6048G= (p.Val2016=) c.5994G= (p.Val1998=) c.5886G= (p.Val1962=) c.5949G= (p.Val1983=) c.5919G= (p.Val1973=) c.5991G= (p.Val1997=) | dbSNP |