ClinVar Miner

List of variants in gene IQCF5 reported as uncertain significance

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Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_001145059.2(IQCF5):c.191A>G (p.Tyr64Cys) rs377036263 0.00033
NM_001145059.2(IQCF5):c.378A>T (p.Gln126His) rs375861159 0.00014
NM_001145059.2(IQCF5):c.283C>T (p.Arg95Cys) rs772101978 0.00011
NM_001145059.2(IQCF5):c.101C>T (p.Ala34Val) rs574300905 0.00009
NM_001145059.2(IQCF5):c.118A>G (p.Ile40Val) rs760253818 0.00008
NM_001145059.2(IQCF5):c.256C>T (p.Arg86Cys) rs756242018 0.00008
NM_001145059.2(IQCF5):c.251G>A (p.Arg84His) rs571907670 0.00006
NM_001145059.2(IQCF5):c.166A>G (p.Arg56Gly) rs1201031687 0.00003
NM_001145059.2(IQCF5):c.305G>A (p.Arg102His) rs766381060 0.00003
NM_001145059.2(IQCF5):c.66G>T (p.Trp22Cys) rs1004426610 0.00003
NM_001145059.2(IQCF5):c.350A>G (p.Glu117Gly) rs780465580 0.00002
NM_001145059.2(IQCF5):c.146T>C (p.Leu49Pro) rs371431499 0.00001
NM_001145059.2(IQCF5):c.277G>A (p.Ala93Thr) rs1443032276 0.00001
NM_001145059.2(IQCF5):c.142G>A (p.Val48Met)
NM_001145059.2(IQCF5):c.268T>G (p.Leu90Val)
NM_001145059.2(IQCF5):c.332T>G (p.Phe111Cys) rs1182270174
NM_001145059.2(IQCF5):c.52A>C (p.Ile18Leu)
NM_001145059.2(IQCF5):c.83G>A (p.Arg28Gln) rs199564539
NM_001145059.2(IQCF5):c.83G>T (p.Arg28Leu) rs199564539
NM_001145059.2(IQCF5):c.85C>G (p.Arg29Gly) rs368521801
NM_001145059.2(IQCF5):c.88A>C (p.Thr30Pro) rs1413165638

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