Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
20 | g.45950453C>A | CA358018 | ZNF335 | c.3332G>T (p.Arg1111Leu) c.3329G>T (p.Arg1110Leu) c.2804G>T (p.Arg935Leu) n.5279G>T n.3728G>T n.3843G>T | ClinVar dbSNP gnomAD v4 |
20 | g.45950453C>T | CA210874 | ZNF335 | c.3332G>A (p.Arg1111His) c.3329G>A (p.Arg1110His) c.2804G>A (p.Arg935His) n.5279G>A n.3728G>A n.3843G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
20 | g.45950453C= | CA2366449599 | ZNF335 | c.3332G= (p.Arg1111=) c.3329G= (p.Arg1110=) c.2804G= (p.Arg935=) n.5279G= n.3728G= n.3843G= | dbSNP |