Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
17	g.37739503_37739577del	CA913190793	HNF1B	c.410_484del (p.Arg137_Lys161del)	ClinVar
17	g.37739567C>A	CA499603955	HNF1B	c.417G>T (p.Val139=)
17	g.37739567C>G	CA499603956	HNF1B	c.417G>C (p.Val139=)
17	g.37739567C>T	CA499603957	HNF1B	c.417G>A (p.Val139=)
17	g.37739568A>C	CA398751523	HNF1B	c.416T>G (p.Val139Gly)	ClinVar
17	g.37739568A>G	CA398751525	HNF1B	c.416T>C (p.Val139Ala)	gnomAD v4
17	g.37739568A>T	CA398751528	HNF1B	c.416T>A (p.Val139Glu)
17	g.37739569C>A	CA398751532	HNF1B	c.415G>T (p.Val139Leu)
17	g.37739569C>G	CA398751534	HNF1B	c.415G>C (p.Val139Leu)
17	g.37739569C>T	CA398751530	HNF1B	c.415G>A (p.Val139Met)
17	g.37739570C>A	CA398751536	HNF1B	c.414G>T (p.Glu138Asp)
17	g.37739570C>G	CA398751537	HNF1B	c.414G>C (p.Glu138Asp)
17	g.37739570C>T	CA499603958	HNF1B	c.414G>A (p.Glu138=)
17	g.37739571T>A	CA398751538	HNF1B	c.413A>T (p.Glu138Val)
17	g.37739571T>C	CA398751539	HNF1B	c.413A>G (p.Glu138Gly)
17	g.37739571T>G	CA398751540	HNF1B	c.413A>C (p.Glu138Ala)
17	g.37739572C>A	CA398751541	HNF1B	c.412G>T (p.Glu138Ter)
17	g.37739572C>G	CA398751543	HNF1B	c.412G>C (p.Glu138Gln)
17	g.37739572C>T	CA398751545	HNF1B	c.412G>A (p.Glu138Lys)
17	g.37739573C>A	CA398751546	HNF1B	c.411G>T (p.Arg137Ser)
17	g.37739573C>G	CA398751548	HNF1B	c.411G>C (p.Arg137Ser)
17	g.37739573C>T	CA499603959	HNF1B	c.411G>A (p.Arg137=)
17	g.37739574C>A	CA398751549	HNF1B	c.410G>T (p.Arg137Met)
17	g.37739574C>G	CA398751551	HNF1B	c.410G>C (p.Arg137Thr)
17	g.37739574C>T	CA398751552	HNF1B	c.410G>A (p.Arg137Lys)	ClinVar dbSNP gnomAD v4
17	g.37739575T>A	CA398751554	HNF1B	c.409A>T (p.Arg137Trp)
17	g.37739575T>C	CA398751555	HNF1B	c.409A>G (p.Arg137Gly)
17	g.37739575T>G	CA499603960	HNF1B	c.409A>C (p.Arg137=)
17	g.37739576C>A	CA398751557	HNF1B	c.408G>T (p.Gln136His)
17	g.37739576C>G	CA398751559	HNF1B	c.408G>C (p.Gln136His)
17	g.37739576C>T	CA499603961	HNF1B	c.408G>A (p.Gln136=)
17	g.37739577T>A	CA398751561	HNF1B	c.407A>T (p.Gln136Leu)
17	g.37739577T>C	CA398751562	HNF1B	c.407A>G (p.Gln136Arg)
17	g.37739577T>G	CA398751564	HNF1B	c.407A>C (p.Gln136Pro)
17	g.37739578G>A	CA398751565	HNF1B	c.406C>T (p.Gln136Ter)	ClinVar
17	g.37739578G>C	CA398751567	HNF1B	c.406C>G (p.Gln136Glu)	ClinVar
17	g.37739578G>T	CA398751568	HNF1B	c.406C>A (p.Gln136Lys)
17	g.37739582dup	CA10603444	HNF1B	c.406dup (p.Gln136ProfsTer?)	ClinVar dbSNP
17	g.37739579G>A	CA499603962	HNF1B	c.405C>T (p.Pro135=)
17	g.37739579G>C	CA499603963	HNF1B	c.405C>G (p.Pro135=)
17	g.37739579G>T	CA499603964	HNF1B	c.405C>A (p.Pro135=)
17	g.37739580G>A	CA398751570	HNF1B	c.404C>T (p.Pro135Leu)
17	g.37739580G>C	CA398751572	HNF1B	c.404C>G (p.Pro135Arg)
17	g.37739580G>T	CA398751573	HNF1B	c.404C>A (p.Pro135His)
17	g.37739581G>A	CA398751578	HNF1B	c.403C>T (p.Pro135Ser)
17	g.37739581G>C	CA398751577	HNF1B	c.403C>G (p.Pro135Ala)
17	g.37739581G>T	CA398751575	HNF1B	c.403C>A (p.Pro135Thr)
17	g.37739582G>A	CA499603965	HNF1B	c.402C>T (p.Ile134=)	ClinVar dbSNP gnomAD v4
17	g.37739582G>C	CA398751580	HNF1B	c.402C>G (p.Ile134Met)
17	g.37739582G>T	CA499603966	HNF1B	c.402C>A (p.Ile134=)	gnomAD v4

Number of alleles fetched