ClinVar Miner

List of variants in gene IFT140 reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 73
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HGVS dbSNP
NM_014714.3(IFT140):c.-328C>T rs528212874
NM_014714.4(IFT140):c.*118G>A rs372303683
NM_014714.4(IFT140):c.*153C>T rs760987640
NM_014714.4(IFT140):c.*158G>C rs886051707
NM_014714.4(IFT140):c.*226T>G rs886051706
NM_014714.4(IFT140):c.*235C>A rs184405274
NM_014714.4(IFT140):c.*23C>T rs752974569
NM_014714.4(IFT140):c.*278C>A rs886051705
NM_014714.4(IFT140):c.*2G>A rs144879630
NM_014714.4(IFT140):c.*429C>T rs192256907
NM_014714.4(IFT140):c.*46T>G rs761282751
NM_014714.4(IFT140):c.-221-6T>A rs886051772
NM_014714.4(IFT140):c.-267G>C rs574385960
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.1646C>T (p.Ser549Phe) rs751137317
NM_014714.4(IFT140):c.1649G>A (p.Arg550Gln) rs762399912
NM_014714.4(IFT140):c.1788T>C (p.Asp596=) rs148904634
NM_014714.4(IFT140):c.1831G>A (p.Val611Ile) rs35301526
NM_014714.4(IFT140):c.1872G>A (p.Thr624=) rs775156902
NM_014714.4(IFT140):c.1959G>A (p.Trp653Ter) rs770731272
NM_014714.4(IFT140):c.2110G>A (p.Gly704Ser)
NM_014714.4(IFT140):c.2360A>G (p.Asp787Gly)
NM_014714.4(IFT140):c.2366A>T (p.Asp789Val) rs1555486589
NM_014714.4(IFT140):c.2423C>T (p.Ala808Val) rs748463111
NM_014714.4(IFT140):c.2424G>A (p.Ala808=) rs375979698
NM_014714.4(IFT140):c.2542C>T (p.Arg848Cys) rs201384469
NM_014714.4(IFT140):c.2561C>T (p.Thr854Met) rs202189990
NM_014714.4(IFT140):c.2578-13C>T rs886051723
NM_014714.4(IFT140):c.2586C>T (p.Ala862=) rs148557575
NM_014714.4(IFT140):c.2650C>T (p.Arg884Trp) rs554196965
NM_014714.4(IFT140):c.2682C>A (p.His894Gln) rs774192784
NM_014714.4(IFT140):c.2682_2683insA (p.His895fs) rs776988446
NM_014714.4(IFT140):c.2781G>A (p.Ser927=) rs773225207
NM_014714.4(IFT140):c.2797G>A (p.Glu933Lys) rs1259402740
NM_014714.4(IFT140):c.2817G>A (p.Ser939=) rs373651150
NM_014714.4(IFT140):c.2908G>A (p.Glu970Lys) rs143720412
NM_014714.4(IFT140):c.2935G>A (p.Glu979Lys) rs146277966
NM_014714.4(IFT140):c.3061G>A (p.Glu1021Lys)
NM_014714.4(IFT140):c.3147C>T (p.Asn1049=) rs150129370
NM_014714.4(IFT140):c.3271-4G>A rs200815296
NM_014714.4(IFT140):c.3385T>C (p.Cys1129Arg) rs886051709
NM_014714.4(IFT140):c.3390C>T (p.Ser1130=) rs765923171
NM_014714.4(IFT140):c.3402C>T (p.Ile1134=) rs761692949
NM_014714.4(IFT140):c.3490A>G (p.Met1164Val) rs369425839
NM_014714.4(IFT140):c.3501C>T (p.Thr1167=) rs377319314
NM_014714.4(IFT140):c.3525C>G (p.Thr1175=) rs752664070
NM_014714.4(IFT140):c.3558G>A (p.Glu1186=) rs368713443
NM_014714.4(IFT140):c.3566G>A (p.Arg1189Gln) rs149837281
NM_014714.4(IFT140):c.3580C>G (p.Gln1194Glu) rs555330165
NM_014714.4(IFT140):c.3584T>C (p.Ile1195Thr) rs753550166
NM_014714.4(IFT140):c.3602G>A (p.Arg1201His) rs147292597
NM_014714.4(IFT140):c.3660+13C>T rs767836990
NM_014714.4(IFT140):c.3668G>A (p.Arg1223Lys) rs751861503
NM_014714.4(IFT140):c.3684C>T (p.Ser1228=) rs146464282
NM_014714.4(IFT140):c.3693G>A (p.Thr1231=) rs144028766
NM_014714.4(IFT140):c.3711C>T (p.Phe1237=) rs146172074
NM_014714.4(IFT140):c.3779G>A (p.Arg1260Gln) rs571556177
NM_014714.4(IFT140):c.3788C>T (p.Pro1263Leu) rs775044452
NM_014714.4(IFT140):c.3861C>T (p.Asp1287=) rs143899594
NM_014714.4(IFT140):c.3874-11C>T rs199887622
NM_014714.4(IFT140):c.3943_3948GCCAAG[2] (p.1315_1316AK[2]) rs746697405
NM_014714.4(IFT140):c.3988G>A (p.Ala1330Thr) rs200699325
NM_014714.4(IFT140):c.3993G>C (p.Gln1331His) rs35823417
NM_014714.4(IFT140):c.4026C>T (p.Phe1342=) rs776522454
NM_014714.4(IFT140):c.4040+10C>T rs138364426
NM_014714.4(IFT140):c.4040+11G>A rs144624901
NM_014714.4(IFT140):c.4148T>C (p.Val1383Ala) rs373499004
NM_014714.4(IFT140):c.4266C>T (p.Ala1422=) rs149359139
NM_014714.4(IFT140):c.4277G>A (p.Gly1426Glu) rs886051708
NM_014714.4(IFT140):c.4278G>T (p.Gly1426=) rs200161877
NM_014714.4(IFT140):c.4318C>T (p.Arg1440Cys) rs758535401
NM_014714.4(IFT140):c.4381G>A (p.Asp1461Asn) rs201065562

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