ClinVar Miner

List of variants in gene ODAD1 reported as benign for Primary ciliary dyskinesia

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Total variants: 45
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HGVS dbSNP gnomAD frequency
NM_001364171.2(ODAD1):c.2019T>C (p.Ser673=) rs7252988 0.59744
NM_001364171.2(ODAD1):c.1582-16T>C rs2292113 0.38553
NM_001364171.2(ODAD1):c.1404+8A>G rs8111947 0.37323
NM_001364171.2(ODAD1):c.666-4G>A rs56177753 0.22521
NM_001364171.2(ODAD1):c.1514C>T (p.Pro505Leu) rs35461177 0.22486
NM_001364171.2(ODAD1):c.1404+20C>A rs8111297 0.19051
NM_001364171.2(ODAD1):c.918C>T (p.Asp306=) rs2242463 0.17921
NM_001364171.2(ODAD1):c.696G>T (p.Leu232=) rs28582401 0.17887
NM_001364171.2(ODAD1):c.1606G>T (p.Ala536Ser) rs61747754 0.14598
NM_001364171.2(ODAD1):c.1176G>A (p.Ser392=) rs34540645 0.05955
NM_001364171.2(ODAD1):c.2024C>T (p.Ser675Leu) rs74925056 0.04566
NM_001364171.2(ODAD1):c.247C>T (p.Arg83Trp) rs16981988 0.03160
NM_001364171.2(ODAD1):c.1097G>A (p.Arg366His) rs35361179 0.02467
NM_001364171.2(ODAD1):c.598-5C>A rs10416590 0.02325
NM_001364171.2(ODAD1):c.1071G>A (p.Glu357=) rs79967289 0.01703
NM_001364171.2(ODAD1):c.1632C>T (p.Ala544=) rs73585332 0.01673
NM_001364171.2(ODAD1):c.1737C>T (p.Pro579=) rs13346323 0.01656
NM_001364171.2(ODAD1):c.825C>T (p.Pro275=) rs34628933 0.01136
NM_001364171.2(ODAD1):c.2027G>A (p.Ser676Asn) rs74351635 0.00931
NM_001364171.2(ODAD1):c.1636G>A (p.Ala546Thr) rs114111020 0.00902
NM_001364171.2(ODAD1):c.1672G>A (p.Ala558Thr) rs115124604 0.00808
NM_001364171.2(ODAD1):c.1214G>A (p.Arg405Gln) rs73585360 0.00719
NM_001364171.2(ODAD1):c.988+11C>A rs112569880 0.00708
NM_001364171.2(ODAD1):c.1275C>T (p.Asp425=) rs35930441 0.00595
NM_001364171.2(ODAD1):c.1788C>T (p.His596=) rs147072026 0.00442
NM_001364171.2(ODAD1):c.730G>A (p.Glu244Lys) rs114078313 0.00421
NM_001364171.2(ODAD1):c.856G>A (p.Gly286Arg) rs73942222 0.00411
NM_001364171.2(ODAD1):c.185G>A (p.Arg62His) rs7248372 0.00372
NM_001364171.2(ODAD1):c.266G>C (p.Arg89Pro) rs58966182 0.00277
NM_001364171.2(ODAD1):c.1481C>T (p.Pro494Leu) rs148823991 0.00171
NM_001364171.2(ODAD1):c.1581+17C>T rs182750626 0.00166
NM_001364171.2(ODAD1):c.582C>T (p.Asp194=) rs190978775 0.00144
NM_001364171.2(ODAD1):c.1425C>T (p.Asp475=) rs150259992 0.00103
NM_001364171.2(ODAD1):c.808G>A (p.Asp270Asn) rs145629439 0.00090
NM_001364171.2(ODAD1):c.1866C>T (p.His622=) rs138562401 0.00087
NM_001364171.2(ODAD1):c.522G>A (p.Ala174=) rs200360777 0.00078
NM_001364171.2(ODAD1):c.1650C>T (p.Asp550=) rs74722451 0.00072
NM_001364171.2(ODAD1):c.1608G>A (p.Ala536=) rs200022799 0.00063
NM_001364171.2(ODAD1):c.555C>T (p.Ile185=) rs114554656 0.00060
NM_001364171.2(ODAD1):c.1630G>A (p.Ala544Thr) rs74413005 0.00042
NM_001364171.2(ODAD1):c.565C>T (p.Arg189Cys) rs538588580 0.00027
NM_001364171.2(ODAD1):c.1680C>A (p.Thr560=) rs138262031 0.00018
NM_001364171.2(ODAD1):c.1702G>A (p.Val568Ile) rs190964996 0.00010
NM_001364171.2(ODAD1):c.708G>A (p.Ala236=) rs755132968 0.00006
NM_001364171.2(ODAD1):c.989-29_989-16del rs774487463

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