ClinVar Miner

List of variants in gene NNT reported as benign for not provided

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Gene type:
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Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_182977.3(NNT):c.46C>T (p.Leu16=) rs10057103 0.64407
NM_182977.3(NNT):c.-26T>C rs12187908 0.23678
NM_182977.3(NNT):c.2142T>C (p.Ala714=) rs56193661 0.06851
NM_182977.3(NNT):c.188A>G (p.Lys63Arg) rs35201656 0.03222
NM_182977.3(NNT):c.1987C>T (p.Leu663Phe) rs41271083 0.03161
NM_182977.3(NNT):c.1098+15G>A rs3764980 0.03160
NM_182977.3(NNT):c.2898A>G (p.Ala966=) rs11539647 0.02570
NM_182977.3(NNT):c.1098+17T>C rs16873430 0.01000
NM_182977.3(NNT):c.2977A>G (p.Ile993Val) rs78818665 0.00637
NM_182977.3(NNT):c.2192C>T (p.Thr731Met) rs75710404 0.00588
NM_182977.3(NNT):c.2634+17A>G rs149583749 0.00248
NM_182977.3(NNT):c.2294-9T>G rs114002702 0.00137
NM_182977.3(NNT):c.129G>C (p.Trp43Cys) rs150553451 0.00009
NM_182977.3(NNT):c.2317C>T (p.Leu773=) rs190213776 0.00006
NM_182977.3(NNT):c.1718-13T>G rs558275721 0.00004
NM_182977.3(NNT):c.1155C>T (p.Ser385=)
NM_182977.3(NNT):c.1377A>G (p.Glu459=)
NM_182977.3(NNT):c.1845T>C (p.Ser615=)
NM_182977.3(NNT):c.2496C>G (p.Pro832=)
NM_182977.3(NNT):c.2876+7G>T rs113092064
NM_182977.3(NNT):c.2902C>A (p.Arg968=) rs146831958
NM_182977.3(NNT):c.382-7dup rs562530333
NM_182977.3(NNT):c.80G>A (p.Arg27His) rs34241095

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