Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.30308851C>TCA255624NR0B1c.513G>A (p.Trp171Ter)
 ClinVar dbSNP
Xg.30308851C>ACA412548603NR0B1c.513G>T (p.Trp171Cys)
 dbSNP gnomAD v2 gnomAD v4
Xg.30308851C=CA2422040618NR0B1c.513G= (p.Trp171=)
 dbSNP

Number of alleles fetched