ClinVar Miner

List of variants in gene PIK3R2 reported as likely benign for not provided

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Gene type:
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Total variants: 45
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HGVS dbSNP gnomAD frequency
NM_005027.4(PIK3R2):c.2127C>T (p.Thr709=) rs112813367 0.04637
NM_005027.4(PIK3R2):c.1737-67G>A rs140819522 0.01052
NM_005027.4(PIK3R2):c.291C>T (p.Pro97=) rs201655779 0.00768
NM_005027.4(PIK3R2):c.1736+12C>T rs112411913 0.00759
NM_005027.4(PIK3R2):c.1416+86T>C rs115949644 0.00622
NM_005027.4(PIK3R2):c.322+223C>T rs115320867 0.00482
NM_005027.4(PIK3R2):c.1560-17C>T rs183117011 0.00461
NM_005027.4(PIK3R2):c.1980-28C>T rs113821701 0.00366
NM_005027.4(PIK3R2):c.323-205A>C rs186116901 0.00354
NM_005027.4(PIK3R2):c.1560-213T>G rs141593307 0.00309
NM_005027.4(PIK3R2):c.160G>A (p.Val54Met) rs201370957 0.00242
NM_005027.4(PIK3R2):c.*6G>A rs557654906 0.00140
NM_005027.4(PIK3R2):c.1938C>T (p.Ile646=) rs146987351 0.00079
NM_005027.4(PIK3R2):c.817A>T (p.Ser273Cys) rs147990742 0.00055
NM_005027.4(PIK3R2):c.2168C>T (p.Pro723Leu) rs201029925 0.00048
NM_005027.4(PIK3R2):c.1023C>T (p.Asn341=) rs201900751 0.00041
NM_005027.4(PIK3R2):c.-18C>T rs148245146 0.00035
NM_005027.4(PIK3R2):c.302G>A (p.Arg101His) rs367971686 0.00031
NM_005027.4(PIK3R2):c.1527C>T (p.Phe509=) rs146837517 0.00020
NM_005027.4(PIK3R2):c.816-8C>T rs200494626 0.00018
NM_005027.4(PIK3R2):c.1191C>T (p.Ser397=) rs201146203 0.00013
NM_005027.4(PIK3R2):c.240C>T (p.Pro80=) rs370853734 0.00013
NM_005027.4(PIK3R2):c.1224G>A (p.Glu408=) rs764436614 0.00007
NM_005027.4(PIK3R2):c.1291-10G>A rs371619761 0.00006
NM_005027.4(PIK3R2):c.1620G>A (p.Thr540=) rs546014325 0.00003
NM_005027.4(PIK3R2):c.2172G>T (p.Pro724=) rs1473627509 0.00003
NM_005027.4(PIK3R2):c.1314C>T (p.Ser438=) rs777290987 0.00001
NM_005027.4(PIK3R2):c.2134C>T (p.Leu712=) rs780181859 0.00001
NM_005027.4(PIK3R2):c.2148G>A (p.Val716=) rs1599991733 0.00001
NM_005027.4(PIK3R2):c.311C>A (p.Ala104Asp) rs770694944 0.00001
NM_005027.4(PIK3R2):c.1182C>G (p.Thr394=)
NM_005027.4(PIK3R2):c.1737-146G>C rs273271
NM_005027.4(PIK3R2):c.1809-8C>A rs376516684
NM_005027.4(PIK3R2):c.1827G>A (p.Glu609=)
NM_005027.4(PIK3R2):c.1830C>T (p.Asp610=) rs1443129832
NM_005027.4(PIK3R2):c.1842C>T (p.Leu614=)
NM_005027.4(PIK3R2):c.2031C>T (p.Phe677=) rs754267384
NM_005027.4(PIK3R2):c.2172G>A (p.Pro724=)
NM_005027.4(PIK3R2):c.241G>A (p.Val81Met)
NM_005027.4(PIK3R2):c.264T>C (p.Pro88=)
NM_005027.4(PIK3R2):c.404T>C (p.Ile135Thr)
NM_005027.4(PIK3R2):c.42G>C (p.Pro14=) rs767495472
NM_005027.4(PIK3R2):c.468C>T (p.Asp156=)
NM_005027.4(PIK3R2):c.500C>G (p.Thr167Arg) rs1176564195
NM_005027.4(PIK3R2):c.891T>C (p.Val297=)

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