ClinVar Miner

List of variants in gene IFT140 reported as benign by Invitae

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Gene type:
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Total variants: 42
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HGVS dbSNP
NM_014714.4(IFT140):c.1541T>A (p.Leu514His) rs150903791
NM_014714.4(IFT140):c.1542C>A (p.Leu514=) rs141542834
NM_014714.4(IFT140):c.1653-14C>T
NM_014714.4(IFT140):c.1667A>G (p.His556Arg) rs137925718
NM_014714.4(IFT140):c.1682G>A (p.Ser561Asn) rs8050974
NM_014714.4(IFT140):c.1788T>C (p.Asp596=) rs148904634
NM_014714.4(IFT140):c.1862G>A (p.Arg621Gln) rs11648609
NM_014714.4(IFT140):c.1918G>A (p.Asp640Asn) rs61742753
NM_014714.4(IFT140):c.1933A>G (p.Asn645Asp) rs540658203
NM_014714.4(IFT140):c.1968T>C (p.Ser656=) rs8048410
NM_014714.4(IFT140):c.2008C>T (p.Pro670Ser) rs34900355
NM_014714.4(IFT140):c.2067+12C>T
NM_014714.4(IFT140):c.2247C>T (p.His749=) rs9930526
NM_014714.4(IFT140):c.2253T>C (p.Pro751=) rs2076436
NM_014714.4(IFT140):c.2330T>G (p.Leu777Arg) rs34535263
NM_014714.4(IFT140):c.2454C>T (p.Asp818=) rs34668993
NM_014714.4(IFT140):c.2493C>T (p.Arg831=)
NM_014714.4(IFT140):c.2550C>T (p.Ala850=) rs2745180
NM_014714.4(IFT140):c.2561C>T (p.Thr854Met) rs202189990
NM_014714.4(IFT140):c.2569G>A (p.Gly857Ser) rs200876696
NM_014714.4(IFT140):c.2742C>T (p.Ser914=) rs374793763
NM_014714.4(IFT140):c.2755C>G (p.Arg919Gly)
NM_014714.4(IFT140):c.2768+18G>A
NM_014714.4(IFT140):c.2829G>A (p.Pro943=) rs141779807
NM_014714.4(IFT140):c.2919C>T (p.Ala973=) rs2235640
NM_014714.4(IFT140):c.2988T>C (p.Asn996=) rs78178397
NM_014714.4(IFT140):c.3079G>A (p.Gly1027Arg) rs137995818
NM_014714.4(IFT140):c.3156C>T (p.Asp1052=)
NM_014714.4(IFT140):c.3209C>T (p.Ala1070Val) rs2235638
NM_014714.4(IFT140):c.3270+19T>C rs2745176
NM_014714.4(IFT140):c.3558G>A (p.Glu1186=) rs368713443
NM_014714.4(IFT140):c.3661-18C>T
NM_014714.4(IFT140):c.3711C>T (p.Phe1237=) rs146172074
NM_014714.4(IFT140):c.3743T>C (p.Ile1248Thr) rs79494390
NM_014714.4(IFT140):c.3861C>T (p.Asp1287=) rs143899594
NM_014714.4(IFT140):c.3874-11C>T rs199887622
NM_014714.4(IFT140):c.3988G>A (p.Ala1330Thr) rs200699325
NM_014714.4(IFT140):c.3990G>A (p.Ala1330=) rs61745103
NM_014714.4(IFT140):c.4040+10C>T rs138364426
NM_014714.4(IFT140):c.4040+11G>A rs144624901
NM_014714.4(IFT140):c.4040+15C>G
NM_014714.4(IFT140):c.4380C>T (p.Asp1460=) rs61749517

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