ClinVar Miner

List of variants in gene IFT140 reported as likely benign for not provided

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Gene type:
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Total variants: 22
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HGVS dbSNP
NM_014714.4(IFT140):c.1527G>A (p.Gly509=) rs777713841
NM_014714.4(IFT140):c.1563G>A (p.Glu521=) rs146356094
NM_014714.4(IFT140):c.1896T>A (p.Thr632=) rs141276689
NM_014714.4(IFT140):c.1944C>T (p.Pro648=) rs763449097
NM_014714.4(IFT140):c.2010G>A (p.Pro670=) rs181881627
NM_014714.4(IFT140):c.2202C>T (p.Pro734=) rs570605676
NM_014714.4(IFT140):c.2544C>T (p.Arg848=) rs371008462
NM_014714.4(IFT140):c.2586C>T (p.Ala862=) rs148557575
NM_014714.4(IFT140):c.2589G>A (p.Glu863=) rs765470612
NM_014714.4(IFT140):c.2616C>T (p.His872=) rs761615768
NM_014714.4(IFT140):c.2865-5C>T rs779711939
NM_014714.4(IFT140):c.2922G>A (p.Ala974=) rs201864536
NM_014714.4(IFT140):c.2997+7T>A rs946595729
NM_014714.4(IFT140):c.2998-4C>A rs764678988
NM_014714.4(IFT140):c.3030G>A (p.Leu1010=) rs775322966
NM_014714.4(IFT140):c.3252G>A (p.Ala1084=) rs375975334
NM_014714.4(IFT140):c.3525C>T (p.Thr1175=) rs752664070
NM_014714.4(IFT140):c.3543G>A (p.Ser1181=) rs377427370
NM_014714.4(IFT140):c.3672G>A (p.Ala1224=) rs765766910
NM_014714.4(IFT140):c.3966C>T (p.Pro1322=) rs181794285
NM_014714.4(IFT140):c.4041-6C>T rs1596295050
NM_014714.4(IFT140):c.4338C>T (p.Asp1446=) rs779634878

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