ClinVar Miner

List of variants in gene KLF10 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_005655.4(KLF10):c.1184-233A>G rs13275089 0.31950
NC_000008.11:g.102656092A>G rs7835270 0.31587
NM_005655.4(KLF10):c.*141C>T rs3191333 0.31025
NM_005655.4(KLF10):c.648A>C (p.Thr216=) rs11552577 0.15075
NM_005655.4(KLF10):c.36+182C>G rs2916570 0.11488
NM_005655.4(KLF10):c.271-22dup rs36083487 0.11267
NC_000008.11:g.102656036G>A rs2734824 0.08819
NM_005655.4(KLF10):c.37-1346C>T rs11779292 0.04730
NM_005655.4(KLF10):c.*167C>T rs75455872 0.02394
NM_005655.4(KLF10):c.1170G>A (p.Thr390=) rs149887425 0.01783
NM_005655.4(KLF10):c.566C>G (p.Thr189Ser) rs28566564 0.00850
NM_005655.4(KLF10):c.557G>T (p.Arg186Ile) rs28634259 0.00849
NM_005655.4(KLF10):c.36+13G>A rs118020675 0.00609
NM_005655.4(KLF10):c.746C>T (p.Ser249Phe) rs4734653 0.00601
NM_005655.4(KLF10):c.1008G>A (p.Pro336=) rs143947106 0.00069
NM_005655.4(KLF10):c.819C>T (p.Ile273=) rs138978474 0.00029
NM_005655.4(KLF10):c.1176G>C (p.Thr392=) rs190177424
NM_005655.4(KLF10):c.1184-17G>T rs142907088
NM_005655.4(KLF10):c.37-74del rs10639139
NM_005655.4(KLF10):c.37-888G>A rs980112
NM_005655.4(KLF10):c.37-93_37-92dup rs10639139
NM_005655.4(KLF10):c.37-93dup rs10639139
NM_005655.4(KLF10):c.674G>A (p.Ser225Asn)

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