Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.173904011G>ACA210762SERPINC1c.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
1g.173904011G=CA1141581236SERPINC1c.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

Number of alleles fetched