ClinVar Miner

List of variants in gene KLF11 reported as benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_003597.5(KLF11):c.*1558T>C rs4669522 0.82295
NM_003597.5(KLF11):c.*1853T>C rs7632 0.55083
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.*194G>A rs76220150 0.00789
NM_003597.5(KLF11):c.*235T>C rs150051327 0.00733
NM_003597.5(KLF11):c.429C>T (p.Ala143=) rs113903638 0.00679
NM_003597.5(KLF11):c.*107G>A rs140559044 0.00616
NM_003597.5(KLF11):c.*981G>A rs148235172 0.00584
NM_003597.5(KLF11):c.*882G>A rs183240123 0.00564
NM_003597.5(KLF11):c.*262C>T rs147746428 0.00373
NM_003597.5(KLF11):c.*241A>G rs191010106 0.00309
NM_003597.5(KLF11):c.*980T>C rs113527829 0.00303
NM_003597.5(KLF11):c.782C>T (p.Pro261Leu) rs148123124 0.00170
NM_003597.5(KLF11):c.*2144C>T rs139703378 0.00157
NM_003597.5(KLF11):c.*2026G>C rs146068438 0.00152
NM_003597.5(KLF11):c.*612C>T rs187519040 0.00045
NM_003597.5(KLF11):c.1448C>T (p.Pro483Leu) rs201735305 0.00023
NM_003597.5(KLF11):c.1450G>A (p.Gly484Ser) rs750063435 0.00006
NM_003597.5(KLF11):c.*192T>C rs552960564 0.00001
NM_003597.5(KLF11):c.*1423T>C rs571234569
NM_003597.5(KLF11):c.*226_*227dup rs34206941

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