Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.38566555G>A | CA017416 | SCN5A | c.3691C>T (p.Arg1231Trp) c.3694C>T (p.Arg1232Trp) c.3532C>T (p.Arg1178Trp) c.3565C>T (p.Arg1189Trp) | ClinVar dbSNP gnomAD v4 |
3 | g.38566555G>C | CA352149406 | SCN5A | c.3691C>G (p.Arg1231Gly) c.3694C>G (p.Arg1232Gly) c.3532C>G (p.Arg1178Gly) c.3565C>G (p.Arg1189Gly) | dbSNP |
3 | g.38566555G= | CA1358569777 | SCN5A | c.3691C= (p.Arg1231=) c.3694C= (p.Arg1232=) c.3532C= (p.Arg1178=) c.3565C= (p.Arg1189=) | dbSNP |