ClinVar Miner

List of variants in gene KLF11 reported as benign for not provided

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Total variants: 27
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HGVS dbSNP gnomAD frequency
NM_003597.5(KLF11):c.1185A>T (p.Val395=) rs11687357 0.82479
NM_003597.5(KLF11):c.*1558T>C rs4669522 0.82295
NM_003597.5(KLF11):c.1259-312C>T rs2487 0.60028
NM_003597.5(KLF11):c.*1853T>C rs7632 0.55083
NM_003597.5(KLF11):c.42+85A>G rs115226520 0.21716
NM_003597.5(KLF11):c.185A>G (p.Gln62Arg) rs35927125 0.08880
NM_003597.5(KLF11):c.*544C>A rs4444493 0.08457
NM_003597.5(KLF11):c.*435A>T rs72786612 0.07883
NM_003597.5(KLF11):c.*1781T>C rs6722205 0.02856
NM_003597.5(KLF11):c.659C>T (p.Thr220Met) rs34336420 0.01310
NM_003597.5(KLF11):c.429C>T (p.Ala143=) rs113903638 0.00679
NM_003597.5(KLF11):c.410A>G (p.Asp137Gly) rs145933214 0.00328
NM_003597.5(KLF11):c.86G>A (p.Arg29Gln) rs150096859 0.00188
NM_003597.5(KLF11):c.225C>T (p.Val75=) rs144083374 0.00158
NM_003597.5(KLF11):c.486A>G (p.Pro162=) rs146462049 0.00093
NM_003597.5(KLF11):c.196C>T (p.Leu66=) rs771505792 0.00002
NM_003597.5(KLF11):c.*226_*227dup rs34206941
NM_003597.5(KLF11):c.*227dup rs34206941
NM_003597.5(KLF11):c.1041C>T (p.Ala347=)
NM_003597.5(KLF11):c.1185= (p.Val395=)
NM_003597.5(KLF11):c.1258+333_1258+335del rs58347649
NM_003597.5(KLF11):c.1258+334_1258+335del rs58347649
NM_003597.5(KLF11):c.1258+335del rs58347649
NM_003597.5(KLF11):c.1258+335dup rs58347649
NM_003597.5(KLF11):c.313-244G>C rs55848997
NM_003597.5(KLF11):c.313-3del rs760634967
NM_003597.5(KLF11):c.42+264G>T rs191862263

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