Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.173904011G>A | CA210762 | SERPINC1 | c.1273C>T (p.Arg425Cys) c.658C>T (p.Arg220Cys) c.1129C>T (p.Arg377Cys) c.1396C>T (p.Arg466Cys) c.1354C>T (p.Arg452Cys) c.1252C>T (p.Arg418Cys) c.1216C>T (p.Arg406Cys) c.1057C>T (p.Arg353Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.173904011G= | CA1141581236 | SERPINC1 | c.1273C= (p.Arg425=) c.658C= (p.Arg220=) c.1129C= (p.Arg377=) c.1396C= (p.Arg466=) c.1354C= (p.Arg452=) c.1252C= (p.Arg418=) c.1216C= (p.Arg406=) c.1057C= (p.Arg353=) | dbSNP |