ClinVar Miner

List of variants in gene HNF1B reported as uncertain significance for Renal cysts and diabetes syndrome

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Total variants: 21
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HGVS dbSNP
NM_000458.4(HNF1B):c.1006C>G (p.His336Asp) rs138986885
NM_000458.4(HNF1B):c.1006C>T (p.His336Tyr) rs138986885
NM_000458.4(HNF1B):c.107C>T (p.Ser36Phe)
NM_000458.4(HNF1B):c.1108G>A (p.Gly370Ser) rs113042313
NM_000458.4(HNF1B):c.130G>A (p.Glu44Lys)
NM_000458.4(HNF1B):c.140C>T (p.Pro47Leu) rs193922483
NM_000458.4(HNF1B):c.1540G>A (p.Ala514Thr)
NM_000458.4(HNF1B):c.1580G>A (p.Arg527Gln) rs758130759
NM_000458.4(HNF1B):c.1610C>A (p.Thr537Asn)
NM_000458.4(HNF1B):c.1657C>A (p.Pro553Thr) rs147798914
NM_000458.4(HNF1B):c.182T>G (p.Val61Gly) rs147816724
NM_000458.4(HNF1B):c.226G>T (p.Gly76Cys) rs144425830
NM_000458.4(HNF1B):c.244G>A (p.Asp82Asn) rs140562402
NM_000458.4(HNF1B):c.499G>A (p.Ala167Thr)
NM_000458.4(HNF1B):c.542G>A (p.Arg181Gln)
NM_000458.4(HNF1B):c.589A>C (p.Ser197Arg)
NM_000458.4(HNF1B):c.662A>T (p.Asp221Val)
NM_000458.4(HNF1B):c.721G>A (p.Ala241Thr) rs761415487
NM_000458.4(HNF1B):c.780G>C (p.Glu260Asp) rs536638039
NM_000458.4(HNF1B):c.949G>T (p.Ala317Ser) rs193922492
NM_000458.4(HNF1B):c.962A>G (p.Asn321Ser) rs193922493

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