ClinVar Miner

List of variants in gene PIK3CD reported as benign for activated PI3K-delta syndrome

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 31
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HGVS dbSNP
NM_005026.5(PIK3CD):c.1002C>T (p.Asn334=) rs28730670
NM_005026.5(PIK3CD):c.1005C>T (p.Ala335=) rs28730671
NM_005026.5(PIK3CD):c.1035C>T (p.Ala345=) rs28730672
NM_005026.5(PIK3CD):c.1366A>G (p.Thr456Ala) rs28730674
NM_005026.5(PIK3CD):c.1394C>T (p.Thr465Met) rs368722127
NM_005026.5(PIK3CD):c.1629G>A (p.Pro543=) rs190710687
NM_005026.5(PIK3CD):c.1689+20T>C rs181919452
NM_005026.5(PIK3CD):c.1710C>T (p.Ser570=) rs200918933
NM_005026.5(PIK3CD):c.1809G>C (p.Leu603=) rs151278626
NM_005026.5(PIK3CD):c.1815C>T (p.Asp605=) rs115808092
NM_005026.5(PIK3CD):c.1863C>T (p.Tyr621=) rs151235777
NM_005026.5(PIK3CD):c.1953C>T (p.Leu651=) rs140468930
NM_005026.5(PIK3CD):c.2094C>T (p.Phe698=) rs370548772
NM_005026.5(PIK3CD):c.2235C>T (p.Cys745=) rs138742347
NM_005026.5(PIK3CD):c.2319C>T (p.Ser773=) rs139848768
NM_005026.5(PIK3CD):c.2426+8C>T rs770571023
NM_005026.5(PIK3CD):c.2427-7T>G rs369339827
NM_005026.5(PIK3CD):c.2808C>T (p.Tyr936=) rs11121484
NM_005026.5(PIK3CD):c.2820T>C (p.His940=) rs28730679
NM_005026.5(PIK3CD):c.2919C>T (p.Leu973=) rs143168081
NM_005026.5(PIK3CD):c.3093G>C (p.Val1031=) rs149090253
NM_005026.5(PIK3CD):c.342C>T (p.Asn114=) rs201273776
NM_005026.5(PIK3CD):c.371-3C>T rs113176101
NM_005026.5(PIK3CD):c.371-5C>T rs149617980
NM_005026.5(PIK3CD):c.436T>A (p.Phe146Ile) rs142285826
NM_005026.5(PIK3CD):c.678A>G (p.Thr226=) rs2230735
NM_005026.5(PIK3CD):c.708G>A (p.Pro236=) rs145697393
NM_005026.5(PIK3CD):c.825C>G (p.Thr275=) rs149175819
NM_005026.5(PIK3CD):c.886G>A (p.Val296Ile) rs28730668
NM_005026.5(PIK3CD):c.931-9G>C rs28730669
NM_005026.5(PIK3CD):c.935C>G (p.Ser312Cys) rs61755420

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