Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.29672739G>C | CA251581 | ZFP57 | c.1372C>G (p.His458Asp) c.1156C>G (p.His386Asp) c.1120C>G (p.His374Asp) c.1312C>G (p.His438Asp) | ClinVar dbSNP |
6 | g.29672739G>T | CA363043352 | ZFP57 | c.1372C>A (p.His458Asn) c.1156C>A (p.His386Asn) c.1120C>A (p.His374Asn) c.1312C>A (p.His438Asn) | dbSNP gnomAD v4 |