ClinVar Miner

List of variants in gene SEC24D reported as likely benign by GeneDx

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 53
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HGVS dbSNP gnomAD frequency
NM_014822.4(SEC24D):c.1422-269A>G rs140348660 0.02449
NM_014822.4(SEC24D):c.1825-130G>A rs17257902 0.01723
NM_014822.4(SEC24D):c.1296+298G>A rs10020345 0.01435
NM_014822.4(SEC24D):c.1708-266T>G rs28391417 0.01016
NM_014822.4(SEC24D):c.2378-79T>C rs73842219 0.01009
NM_014822.4(SEC24D):c.1995+92G>T rs11098448 0.01007
NM_014822.4(SEC24D):c.2677-166G>A rs114860709 0.00955
NM_014822.4(SEC24D):c.653C>G (p.Ala218Gly) rs35392900 0.00940
NM_014822.4(SEC24D):c.2378-38G>C rs73842217 0.00937
NM_014822.4(SEC24D):c.2677-264T>A rs139254700 0.00885
NM_014822.4(SEC24D):c.248+181G>C rs182120464 0.00865
NM_014822.4(SEC24D):c.1041+214G>A rs28650354 0.00852
NM_014822.4(SEC24D):c.2959-288C>G rs58619091 0.00811
NM_014822.4(SEC24D):c.*172A>G rs79586191 0.00750
NM_014822.4(SEC24D):c.1421+249T>A rs78056828 0.00748
NM_014822.4(SEC24D):c.1297-228A>G rs10029461 0.00742
NM_014822.4(SEC24D):c.1825-29T>A rs115973812 0.00704
NM_014822.4(SEC24D):c.2377+302C>G rs116021794 0.00700
NM_014822.4(SEC24D):c.1825-66T>A rs115727462 0.00686
NM_014822.4(SEC24D):c.802-254A>G rs79357895 0.00630
NM_014822.4(SEC24D):c.1884C>T (p.His628=) rs80266466 0.00605
NM_014822.4(SEC24D):c.139C>T (p.Pro47Ser) rs116357076 0.00546
NM_014822.4(SEC24D):c.2528C>T (p.Pro843Leu) rs76658950 0.00513
NM_014822.4(SEC24D):c.1707+69T>C rs78672826 0.00509
NM_014822.4(SEC24D):c.118+331T>C rs113904850 0.00498
NM_014822.4(SEC24D):c.397+272T>C rs182430827 0.00498
NM_014822.4(SEC24D):c.398-112G>A rs139589277 0.00479
NM_014822.4(SEC24D):c.1440G>A (p.Thr480=) rs116723900 0.00459
NM_014822.4(SEC24D):c.248+7T>C rs139956480 0.00453
NM_014822.4(SEC24D):c.1995+141C>T rs142075154 0.00446
NM_014822.4(SEC24D):c.1996-114T>A rs185572459 0.00435
NM_014822.4(SEC24D):c.2238+161G>T rs184458179 0.00433
NM_014822.4(SEC24D):c.2959-16G>T rs58916284 0.00425
NM_014822.4(SEC24D):c.2536A>G (p.Met846Val) rs34510328 0.00412
NM_014822.4(SEC24D):c.2378-24C>T rs191180306 0.00408
NM_014822.4(SEC24D):c.1421+111T>A rs116022113 0.00336
NM_014822.4(SEC24D):c.700G>A (p.Ala234Thr) rs73842254 0.00315
NM_014822.4(SEC24D):c.914-33C>G rs114662287 0.00293
NM_014822.4(SEC24D):c.429C>T (p.Pro143=) rs150602522 0.00155
NM_014822.4(SEC24D):c.2496+31G>A rs183110720 0.00149
NM_014822.4(SEC24D):c.2681C>T (p.Thr894Met) rs149063473 0.00116
NM_014822.4(SEC24D):c.2135A>C (p.Asn712Thr) rs146773641 0.00071
NM_014822.4(SEC24D):c.1614-29C>G rs559986891 0.00052
NM_014822.4(SEC24D):c.1929C>T (p.Asp643=) rs112206247 0.00051
NM_014822.4(SEC24D):c.2184C>T (p.Thr728=) rs775479247 0.00011
NM_014822.4(SEC24D):c.1825-32A>C rs28627331
NM_014822.4(SEC24D):c.1996-242G>A rs116448075
NM_014822.4(SEC24D):c.2677-21C>G rs149598210
NM_014822.4(SEC24D):c.2784C>T (p.Phe928=) rs79301273
NM_014822.4(SEC24D):c.2868+64_2868+67del rs201791424
NM_014822.4(SEC24D):c.2868+99_2868+101del rs141678608
NM_014822.4(SEC24D):c.801+130del rs145852532
NM_014822.4(SEC24D):c.801+231del rs892083650

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