Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.37744584C>ACA122599HNF1Bc.301G>T (p.Glu101Ter)
 ClinVar dbSNP
17g.37744584C>GCA8519119HNF1Bc.301G>C (p.Glu101Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
17g.37744584C=CA3223280491HNF1Bc.301G= (p.Glu101=)
 dbSNP

Number of alleles fetched