ClinVar Miner

List of variants reported as uncertain significance for Renal cysts and diabetes syndrome; Type 2 diabetes mellitus; Nonpapillary renal cell carcinoma

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Total variants: 63
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HGVS dbSNP gnomAD frequency
NM_000458.4(HNF1B):c.1657C>A (p.Pro553Thr) rs147798914 0.00016
NM_000458.4(HNF1B):c.1654-9T>A rs200579660 0.00009
NM_000458.4(HNF1B):c.107C>T (p.Ser36Phe) rs544890850 0.00005
NM_000458.4(HNF1B):c.780G>C (p.Glu260Asp) rs536638039 0.00005
NM_000458.4(HNF1B):c.1033A>G (p.Asn345Asp) rs755951130 0.00003
NM_000458.4(HNF1B):c.1207A>T (p.Ile403Phe) rs747110790 0.00003
NM_000458.4(HNF1B):c.953A>G (p.Tyr318Cys) rs752340487 0.00003
NM_000458.4(HNF1B):c.1390G>A (p.Gly464Ser) rs982085453 0.00002
NM_000458.4(HNF1B):c.140C>T (p.Pro47Leu) rs193922483 0.00002
NM_000458.4(HNF1B):c.516C>T (p.Tyr172=) rs764561297 0.00002
NM_000458.4(HNF1B):c.721G>A (p.Ala241Thr) rs761415487 0.00002
NM_000458.4(HNF1B):c.1025C>T (p.Ser342Phe) rs780035561 0.00001
NM_000458.4(HNF1B):c.1117G>A (p.Ala373Thr) rs759270956 0.00001
NM_000458.4(HNF1B):c.1305G>T (p.Met435Ile) rs1199229728 0.00001
NM_000458.4(HNF1B):c.191C>G (p.Thr64Ser) rs750176807 0.00001
NM_000458.4(HNF1B):c.231C>G (p.Asp77Glu) rs760448993 0.00001
NM_000458.4(HNF1B):c.305A>C (p.Glu102Ala) rs982165538 0.00001
NM_000458.4(HNF1B):c.34C>T (p.Leu12Phe) rs1285239018 0.00001
NM_000458.4(HNF1B):c.592A>C (p.Ser198Arg) rs1321074352 0.00001
NM_000458.4(HNF1B):c.78G>T (p.Leu26=) rs757790704 0.00001
NM_000458.4(HNF1B):c.988C>T (p.Leu330Phe) rs763078496 0.00001
NM_000458.4(HNF1B):c.*73G>A
NM_000458.4(HNF1B):c.1006C>T (p.His336Tyr) rs138986885
NM_000458.4(HNF1B):c.1013A>G (p.Gln338Arg)
NM_000458.4(HNF1B):c.1024T>C (p.Ser342Pro) rs1282596664
NM_000458.4(HNF1B):c.1038G>A (p.Lys346=)
NM_000458.4(HNF1B):c.1046G>A (p.Gly349Glu)
NM_000458.4(HNF1B):c.1051C>T (p.Arg351Cys)
NM_000458.4(HNF1B):c.1062G>T (p.Gln354His) rs202109472
NM_000458.4(HNF1B):c.1121T>C (p.Met374Thr)
NM_000458.4(HNF1B):c.116T>A (p.Phe39Tyr)
NM_000458.4(HNF1B):c.1196A>G (p.Asp399Gly)
NM_000458.4(HNF1B):c.1213G>C (p.Val405Leu)
NM_000458.4(HNF1B):c.1365T>G (p.Ser455Arg)
NM_000458.4(HNF1B):c.1399G>A (p.Ala467Thr)
NM_000458.4(HNF1B):c.1493A>C (p.Gln498Pro)
NM_000458.4(HNF1B):c.1507G>C (p.Ala503Pro)
NM_000458.4(HNF1B):c.1525A>C (p.Asn509His) rs2511700041
NM_000458.4(HNF1B):c.1543C>T (p.His515Tyr) rs1188569241
NM_000458.4(HNF1B):c.1544A>G (p.His515Arg)
NM_000458.4(HNF1B):c.1562A>G (p.Gln521Arg)
NM_000458.4(HNF1B):c.171C>A (p.Asp57Glu)
NM_000458.4(HNF1B):c.193C>T (p.Leu65Phe)
NM_000458.4(HNF1B):c.315G>T (p.Glu105Asp)
NM_000458.4(HNF1B):c.332A>G (p.Asp111Gly) rs1311605355
NM_000458.4(HNF1B):c.377A>G (p.Lys126Arg)
NM_000458.4(HNF1B):c.385A>G (p.Met129Val)
NM_000458.4(HNF1B):c.538C>T (p.Leu180Phe)
NM_000458.4(HNF1B):c.544+5G>A rs2511827891
NM_000458.4(HNF1B):c.544C>G (p.Gln182Glu)
NM_000458.4(HNF1B):c.577A>T (p.Met193Leu)
NM_000458.4(HNF1B):c.578T>C (p.Met193Thr) rs760079000
NM_000458.4(HNF1B):c.601C>G (p.Gln201Glu)
NM_000458.4(HNF1B):c.622G>C (p.Glu208Gln)
NM_000458.4(HNF1B):c.658G>A (p.Asp220Asn)
NM_000458.4(HNF1B):c.658G>C (p.Asp220His) rs377555356
NM_000458.4(HNF1B):c.68A>G (p.Lys23Arg) rs2511853122
NM_000458.4(HNF1B):c.694C>T (p.Arg232Cys) rs766793933
NM_000458.4(HNF1B):c.695G>A (p.Arg232His)
NM_000458.4(HNF1B):c.754C>T (p.Arg252Trp) rs748416956
NM_000458.4(HNF1B):c.949G>A (p.Ala317Thr)
NM_000458.4(HNF1B):c.995A>G (p.His332Arg)
NM_000458.4(HNF1B):c.997G>A (p.Gly333Ser)

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