ClinVar Miner

List of variants in gene IFI44L reported as uncertain significance by Ambry Genetics

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Gene type:
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Total variants: 45
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HGVS dbSNP gnomAD frequency
NM_006820.4(IFI44L):c.61A>T (p.Asn21Tyr) rs372310725 0.00027
NM_006820.4(IFI44L):c.1088G>A (p.Cys363Tyr) rs142635614 0.00023
NM_006820.4(IFI44L):c.817G>A (p.Gly273Arg) rs139875914 0.00016
NM_006820.4(IFI44L):c.818G>T (p.Gly273Val) rs138987531 0.00014
NM_006820.4(IFI44L):c.1147C>T (p.Arg383Trp) rs771809041 0.00005
NM_006820.4(IFI44L):c.475G>C (p.Glu159Gln) rs368426493 0.00005
NM_006820.4(IFI44L):c.1091G>A (p.Ser364Asn) rs1002531253 0.00002
NM_006820.4(IFI44L):c.1184T>C (p.Ile395Thr) rs753970944 0.00002
NM_006820.4(IFI44L):c.1301A>G (p.Glu434Gly) rs754061177 0.00002
NM_006820.4(IFI44L):c.56T>A (p.Leu19His) rs748219494 0.00002
NM_006820.4(IFI44L):c.1005G>A (p.Met335Ile) rs376331794 0.00001
NM_006820.4(IFI44L):c.1163A>G (p.His388Arg) rs762172392 0.00001
NM_006820.4(IFI44L):c.1183A>G (p.Ile395Val) rs955407884 0.00001
NM_006820.4(IFI44L):c.1198A>T (p.Met400Leu) rs758261571 0.00001
NM_006820.4(IFI44L):c.122T>C (p.Val41Ala) rs765587785 0.00001
NM_006820.4(IFI44L):c.1282G>T (p.Ala428Ser) rs750831210 0.00001
NM_006820.4(IFI44L):c.173A>G (p.Tyr58Cys) rs780100161 0.00001
NM_006820.4(IFI44L):c.779T>G (p.Leu260Trp) rs1434616567 0.00001
NM_006820.4(IFI44L):c.932C>G (p.Ser311Cys) rs779446092 0.00001
NM_006820.4(IFI44L):c.958G>A (p.Ala320Thr) rs773410100 0.00001
NM_006820.4(IFI44L):c.107G>A (p.Ser36Asn) rs372837467
NM_006820.4(IFI44L):c.1118A>G (p.Asn373Ser)
NM_006820.4(IFI44L):c.1154T>C (p.Met385Thr)
NM_006820.4(IFI44L):c.1181C>T (p.Pro394Leu)
NM_006820.4(IFI44L):c.1279C>T (p.Arg427Trp)
NM_006820.4(IFI44L):c.1280G>A (p.Arg427Gln) rs373251848
NM_006820.4(IFI44L):c.1319A>G (p.Glu440Gly)
NM_006820.4(IFI44L):c.14C>T (p.Thr5Ile) rs375524121
NM_006820.4(IFI44L):c.211A>G (p.Asn71Asp)
NM_006820.4(IFI44L):c.278C>G (p.Thr93Ser)
NM_006820.4(IFI44L):c.305A>G (p.Asn102Ser)
NM_006820.4(IFI44L):c.317A>G (p.Lys106Arg) rs2523334554
NM_006820.4(IFI44L):c.356C>A (p.Thr119Lys)
NM_006820.4(IFI44L):c.443G>A (p.Arg148His) rs141849276
NM_006820.4(IFI44L):c.470G>A (p.Arg157Gln)
NM_006820.4(IFI44L):c.502A>G (p.Ile168Val) rs1449108356
NM_006820.4(IFI44L):c.530A>G (p.His177Arg)
NM_006820.4(IFI44L):c.550G>C (p.Asp184His) rs753372312
NM_006820.4(IFI44L):c.646T>C (p.Ser216Pro)
NM_006820.4(IFI44L):c.718G>A (p.Glu240Lys)
NM_006820.4(IFI44L):c.811G>A (p.Gly271Arg)
NM_006820.4(IFI44L):c.886C>A (p.Arg296Ser)
NM_006820.4(IFI44L):c.953G>C (p.Cys318Ser) rs374146000
NM_006820.4(IFI44L):c.98A>C (p.His33Pro) rs143352734
NM_006820.4(IFI44L):c.991C>A (p.Leu331Ile)

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