ClinVar Miner

List of variants in gene IQCB1 reported as uncertain significance for Senior-Loken syndrome 5

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Total variants: 35
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HGVS dbSNP
NM_001023570.4(IQCB1):c.*148T>C
NM_001023570.4(IQCB1):c.*151T>C
NM_001023570.4(IQCB1):c.*160C>T
NM_001023570.4(IQCB1):c.*218G>A
NM_001023570.4(IQCB1):c.*226T>C rs886057822
NM_001023570.4(IQCB1):c.*327T>C
NM_001023570.4(IQCB1):c.*399A>G
NM_001023570.4(IQCB1):c.-12-4A>T
NM_001023570.4(IQCB1):c.-154T>G rs886057830
NM_001023570.4(IQCB1):c.-179G>A
NM_001023570.4(IQCB1):c.-185C>G rs553719849
NM_001023570.4(IQCB1):c.-190C>T rs145282757
NM_001023570.4(IQCB1):c.1129+13A>G rs371443898
NM_001023570.4(IQCB1):c.1135G>A (p.Val379Met) rs886057825
NM_001023570.4(IQCB1):c.1150C>T (p.Arg384Trp)
NM_001023570.4(IQCB1):c.1278+7C>T rs112780863
NM_001023570.4(IQCB1):c.1441G>A (p.Glu481Lys) rs140630401
NM_001023570.4(IQCB1):c.1466G>A (p.Arg489Gln)
NM_001023570.4(IQCB1):c.1544G>T (p.Ser515Ile) rs886057823
NM_001023570.4(IQCB1):c.1549A>T (p.Asn517Tyr) rs139468837
NM_001023570.4(IQCB1):c.1595G>A (p.Gly532Glu) rs200719828
NM_001023570.4(IQCB1):c.1611C>T (p.Leu537=) rs373762948
NM_001023570.4(IQCB1):c.1656C>G (p.Ala552=)
NM_001023570.4(IQCB1):c.169G>T (p.Asp57Tyr)
NM_001023570.4(IQCB1):c.1739A>C (p.Lys580Thr) rs199775360
NM_001023570.4(IQCB1):c.348A>G (p.Leu116=) rs139299149
NM_001023570.4(IQCB1):c.358A>T (p.Arg120Ter) rs1372460709
NM_001023570.4(IQCB1):c.482A>G (p.Gln161Arg) rs376700204
NM_001023570.4(IQCB1):c.714T>C (p.Ala238=) rs886057828
NM_001023570.4(IQCB1):c.722A>G (p.His241Arg) rs886057827
NM_001023570.4(IQCB1):c.782T>G (p.Leu261Arg)
NM_001023570.4(IQCB1):c.791A>C (p.Gln264Pro)
NM_001023570.4(IQCB1):c.814C>G (p.Gln272Glu) rs760296374
NM_001023570.4(IQCB1):c.823A>G (p.Arg275Gly) rs886057826
NM_001023570.4(IQCB1):c.877-11C>T rs192296154

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