ClinVar Miner

List of variants in gene PIK3CD reported as benign for hematologic disorder

Included ClinVar conditions (819):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 54
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HGVS dbSNP gnomAD frequency
NM_005026.5(PIK3CD):c.2348-30C>T rs11589267 0.33011
NM_005026.5(PIK3CD):c.2808C>T (p.Tyr936=) rs11121484 0.22663
NM_005026.5(PIK3CD):c.678A>G (p.Thr226=) rs2230735 0.03898
NM_005026.5(PIK3CD):c.886G>A (p.Val296Ile) rs28730668 0.02942
NM_005026.5(PIK3CD):c.1522-19T>C rs77571929 0.02260
NM_005026.5(PIK3CD):c.1689+20T>C rs181919452 0.02153
NM_005026.5(PIK3CD):c.935C>G (p.Ser312Cys) rs61755420 0.01937
NM_005026.5(PIK3CD):c.371-3C>T rs113176101 0.01792
NM_005026.5(PIK3CD):c.931-9G>C rs28730669 0.01748
NM_005026.5(PIK3CD):c.2319C>T (p.Ser773=) rs139848768 0.01195
NM_005026.5(PIK3CD):c.1953C>T (p.Leu651=) rs140468930 0.00813
NM_005026.5(PIK3CD):c.1002C>T (p.Asn334=) rs28730670 0.00506
NM_005026.5(PIK3CD):c.1005C>T (p.Ala335=) rs28730671 0.00483
NM_005026.5(PIK3CD):c.708G>A (p.Pro236=) rs145697393 0.00469
NM_005026.5(PIK3CD):c.2820T>C (p.His940=) rs28730679 0.00350
NM_005026.5(PIK3CD):c.1809G>C (p.Leu603=) rs151278626 0.00268
NM_005026.5(PIK3CD):c.2235C>T (p.Cys745=) rs138742347 0.00252
NM_005026.5(PIK3CD):c.1863C>T (p.Tyr621=) rs151235777 0.00139
NM_005026.5(PIK3CD):c.1470+13C>T rs553468301 0.00120
NM_005026.5(PIK3CD):c.436T>A (p.Phe146Ile) rs142285826 0.00117
NM_005026.5(PIK3CD):c.2919C>T (p.Leu973=) rs143168081 0.00114
NM_005026.5(PIK3CD):c.3093G>C (p.Val1031=) rs149090253 0.00113
NM_005026.5(PIK3CD):c.1815C>T (p.Asp605=) rs115808092 0.00085
NM_005026.5(PIK3CD):c.1812-17G>A rs201032317 0.00083
NM_005026.5(PIK3CD):c.371-5C>T rs149617980 0.00064
NM_005026.5(PIK3CD):c.3114G>A (p.Val1038=) rs138398486 0.00053
NM_005026.5(PIK3CD):c.825C>G (p.Thr275=) rs149175819 0.00043
NM_005026.5(PIK3CD):c.2427-7T>G rs369339827 0.00038
NM_005026.5(PIK3CD):c.2094C>T (p.Phe698=) rs370548772 0.00036
NM_005026.5(PIK3CD):c.2865-19C>T rs371194095 0.00012
NM_005026.5(PIK3CD):c.1470+16G>A rs573337389 0.00011
NM_005026.5(PIK3CD):c.2998-15G>A rs200233248 0.00009
NM_005026.5(PIK3CD):c.1629G>A (p.Pro543=) rs190710687 0.00007
NM_005026.5(PIK3CD):c.342C>T (p.Asn114=) rs201273776 0.00007
NM_005026.5(PIK3CD):c.1824G>A (p.Leu608=) rs778839252 0.00005
NM_005026.5(PIK3CD):c.600+13G>A rs768012867 0.00005
NM_005026.5(PIK3CD):c.142-12C>T rs140984297 0.00004
NM_005026.5(PIK3CD):c.1785C>T (p.Phe595=) rs375016049 0.00004
NM_005026.5(PIK3CD):c.2998-18G>A rs554946921 0.00004
NM_005026.5(PIK3CD):c.558G>A (p.Pro186=) rs748818520 0.00004
NM_005026.5(PIK3CD):c.1470+15C>T rs375880685 0.00003
NM_005026.5(PIK3CD):c.1635G>A (p.Ala545=) rs769971778 0.00003
NM_005026.5(PIK3CD):c.849C>T (p.Leu283=) rs376128746 0.00003
NM_005026.5(PIK3CD):c.1710C>T (p.Ser570=) rs200918933 0.00001
NM_005026.5(PIK3CD):c.252C>T (p.Asp84=) rs755377648 0.00001
NM_005026.5(PIK3CD):c.1020+15_1020+18dup rs755190125
NM_005026.5(PIK3CD):c.163T>G (p.Tyr55Asp)
NM_005026.5(PIK3CD):c.1764C>T (p.Pro588=)
NM_005026.5(PIK3CD):c.2085G>A (p.Leu695=)
NM_005026.5(PIK3CD):c.2426+8C>T rs770571023
NM_005026.5(PIK3CD):c.2427-9del
NM_005026.5(PIK3CD):c.2864+19del
NM_005026.5(PIK3CD):c.2998-8G>T rs546505883
NM_005026.5(PIK3CD):c.781-8del rs2100866754

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