ClinVar Miner

List of variants in gene PIK3C2G reported as uncertain significance

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Total variants: 103
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HGVS dbSNP gnomAD frequency
NM_001288772.2(PIK3C2G):c.205C>T (p.Pro69Ser) rs201018498 0.00046
NM_001288772.2(PIK3C2G):c.2149T>C (p.Tyr717His) rs200263951 0.00030
NM_001288772.2(PIK3C2G):c.2308A>T (p.Thr770Ser) rs369497823 0.00028
NM_001288772.2(PIK3C2G):c.2231A>G (p.Glu744Gly) rs746411737 0.00019
NM_001288772.2(PIK3C2G):c.2039C>G (p.Ser680Cys) rs375035027 0.00016
NM_001288772.2(PIK3C2G):c.1003A>C (p.Ser335Arg) rs200790997 0.00015
NM_001288772.2(PIK3C2G):c.2264G>A (p.Arg755Lys) rs374637655 0.00015
NM_001288772.2(PIK3C2G):c.22G>T (p.Asp8Tyr) rs201177662 0.00014
NM_001288772.2(PIK3C2G):c.2629A>C (p.Lys877Gln) rs746849167 0.00014
NM_001288772.2(PIK3C2G):c.1077A>T (p.Lys359Asn) rs373231729 0.00013
NM_001288772.2(PIK3C2G):c.3334C>T (p.Pro1112Ser) rs372642230 0.00011
NM_001288772.2(PIK3C2G):c.2714T>G (p.Leu905Arg) rs387907449 0.00009
NM_001288772.2(PIK3C2G):c.3459G>A (p.Leu1153=) rs375555307 0.00006
NM_001288772.2(PIK3C2G):c.2903G>A (p.Arg968His) rs750864969 0.00005
NM_001288772.2(PIK3C2G):c.3946A>G (p.Arg1316Gly) rs200838936 0.00005
NM_001288772.2(PIK3C2G):c.868A>G (p.Ile290Val) rs367579213 0.00005
NM_001288772.2(PIK3C2G):c.2534A>G (p.Tyr845Cys) rs1392293386 0.00004
NM_001288772.2(PIK3C2G):c.10T>C (p.Ser4Pro) rs774197612 0.00003
NM_001288772.2(PIK3C2G):c.1279G>A (p.Val427Met) rs756781973 0.00003
NM_001288772.2(PIK3C2G):c.3822C>A (p.Ser1274Arg) rs387907451 0.00003
NM_001288772.2(PIK3C2G):c.1944G>C (p.Met648Ile) rs765563747 0.00002
NM_001288772.2(PIK3C2G):c.3952T>C (p.Phe1318Leu) rs71539452 0.00002
NM_001288772.2(PIK3C2G):c.439T>C (p.Ser147Pro) rs779733977 0.00002
NM_001288772.2(PIK3C2G):c.1396A>G (p.Asn466Asp) rs774136829 0.00001
NM_001288772.2(PIK3C2G):c.1448C>T (p.Thr483Ile) rs1324139872 0.00001
NM_001288772.2(PIK3C2G):c.1505A>G (p.Tyr502Cys) rs752464101 0.00001
NM_001288772.2(PIK3C2G):c.2293G>A (p.Ala765Thr) rs758616836 0.00001
NM_001288772.2(PIK3C2G):c.2458C>T (p.Leu820Phe) rs754014756 0.00001
NM_001288772.2(PIK3C2G):c.2797T>C (p.Cys933Arg) rs1940982855 0.00001
NM_001288772.2(PIK3C2G):c.2918T>C (p.Val973Ala) rs387907453 0.00001
NM_001288772.2(PIK3C2G):c.2969A>G (p.Asp990Gly) rs771793429 0.00001
NM_001288772.2(PIK3C2G):c.313C>A (p.Pro105Thr) rs746898871 0.00001
NM_001288772.2(PIK3C2G):c.3703C>G (p.Gln1235Glu) rs1326059090 0.00001
NM_001288772.2(PIK3C2G):c.3865C>A (p.Gln1289Lys) rs1160725015 0.00001
NM_001288772.2(PIK3C2G):c.3911A>G (p.His1304Arg) rs374207613 0.00001
NM_001288772.2(PIK3C2G):c.457A>G (p.Lys153Glu) rs748292087 0.00001
GRCh37/hg19 12p12.3(chr12:18358097-18681102)x1
GRCh37/hg19 12p12.3(chr12:18531123-18603085)
GRCh37/hg19 12p12.3(chr12:18636979-18799315)x1
GRCh37/hg19 12p12.3(chr12:18664472-18759382)x1
NM_001288772.2(PIK3C2G):c.1031A>G (p.Gln344Arg) rs2498432263
NM_001288772.2(PIK3C2G):c.1071A>C (p.Lys357Asn) rs762493710
NM_001288772.2(PIK3C2G):c.1177C>A (p.Leu393Ile) rs1444567095
NM_001288772.2(PIK3C2G):c.1453G>C (p.Glu485Gln)
NM_001288772.2(PIK3C2G):c.1477C>A (p.Leu493Ile)
NM_001288772.2(PIK3C2G):c.1538G>T (p.Cys513Phe)
NM_001288772.2(PIK3C2G):c.1894G>C (p.Gly632Arg) rs537382833
NM_001288772.2(PIK3C2G):c.2000A>G (p.Asp667Gly) rs761050780
NM_001288772.2(PIK3C2G):c.2095G>T (p.Ala699Ser)
NM_001288772.2(PIK3C2G):c.2119C>A (p.Pro707Thr) rs111580027
NM_001288772.2(PIK3C2G):c.2207T>C (p.Leu736Pro)
NM_001288772.2(PIK3C2G):c.221C>T (p.Thr74Ile)
NM_001288772.2(PIK3C2G):c.2252A>C (p.His751Pro) rs2499408161
NM_001288772.2(PIK3C2G):c.2335C>A (p.Arg779Ser)
NM_001288772.2(PIK3C2G):c.233T>C (p.Leu78Ser) rs2498276879
NM_001288772.2(PIK3C2G):c.2419T>G (p.Phe807Val) rs2499597927
NM_001288772.2(PIK3C2G):c.2464C>T (p.Arg822Cys)
NM_001288772.2(PIK3C2G):c.2489C>T (p.Ala830Val) rs2499598727
NM_001288772.2(PIK3C2G):c.2516A>T (p.Asn839Ile) rs1011605430
NM_001288772.2(PIK3C2G):c.263A>G (p.Glu88Gly) rs750826408
NM_001288772.2(PIK3C2G):c.2674C>T (p.His892Tyr)
NM_001288772.2(PIK3C2G):c.2705T>C (p.Ile902Thr)
NM_001288772.2(PIK3C2G):c.2760C>G (p.Asn920Lys) rs1288890184
NM_001288772.2(PIK3C2G):c.2791G>A (p.Asp931Asn)
NM_001288772.2(PIK3C2G):c.2809A>T (p.Thr937Ser) rs387907452
NM_001288772.2(PIK3C2G):c.2873G>A (p.Ser958Asn)
NM_001288772.2(PIK3C2G):c.2902C>T (p.Arg968Cys)
NM_001288772.2(PIK3C2G):c.2908G>A (p.Asp970Asn) rs2500020794
NM_001288772.2(PIK3C2G):c.2944A>C (p.Asn982His)
NM_001288772.2(PIK3C2G):c.2968G>T (p.Asp990Tyr) rs372973983
NM_001288772.2(PIK3C2G):c.3112T>C (p.Trp1038Arg)
NM_001288772.2(PIK3C2G):c.3179G>T (p.Cys1060Phe) rs771440899
NM_001288772.2(PIK3C2G):c.3206T>A (p.Ile1069Asn) rs377020826
NM_001288772.2(PIK3C2G):c.3223C>T (p.Arg1075Cys)
NM_001288772.2(PIK3C2G):c.3276C>G (p.Asp1092Glu) rs1592435519
NM_001288772.2(PIK3C2G):c.328A>G (p.Ser110Gly)
NM_001288772.2(PIK3C2G):c.3453C>A (p.Ser1151Arg) rs1303514822
NM_001288772.2(PIK3C2G):c.3480+1G>T rs907142477
NM_001288772.2(PIK3C2G):c.359C>A (p.Thr120Lys)
NM_001288772.2(PIK3C2G):c.3614G>C (p.Cys1205Ser)
NM_001288772.2(PIK3C2G):c.3632A>G (p.Asn1211Ser)
NM_001288772.2(PIK3C2G):c.3694A>G (p.Thr1232Ala)
NM_001288772.2(PIK3C2G):c.3719T>C (p.Leu1240Pro) rs2498001251
NM_001288772.2(PIK3C2G):c.371G>A (p.Cys124Tyr)
NM_001288772.2(PIK3C2G):c.3816A>G (p.Glu1272=) rs387907450
NM_001288772.2(PIK3C2G):c.3844C>G (p.Gln1282Glu)
NM_001288772.2(PIK3C2G):c.4019G>C (p.Cys1340Ser) rs1947250041
NM_001288772.2(PIK3C2G):c.4031T>A (p.Phe1344Tyr)
NM_001288772.2(PIK3C2G):c.4045G>A (p.Ala1349Thr) rs1243792370
NM_001288772.2(PIK3C2G):c.4063G>A (p.Glu1355Lys)
NM_001288772.2(PIK3C2G):c.4131A>G (p.Ile1377Met)
NM_001288772.2(PIK3C2G):c.4183C>G (p.His1395Asp) rs1261266228
NM_001288772.2(PIK3C2G):c.4249G>T (p.Val1417Phe)
NM_001288772.2(PIK3C2G):c.4265C>T (p.Thr1422Ile)
NM_001288772.2(PIK3C2G):c.455A>G (p.Asp152Gly) rs1388591295
NM_001288772.2(PIK3C2G):c.484A>C (p.Asn162His) rs762601548
NM_001288772.2(PIK3C2G):c.558C>A (p.Phe186Leu)
NM_001288772.2(PIK3C2G):c.587G>T (p.Gly196Val)
NM_001288772.2(PIK3C2G):c.640C>T (p.Pro214Ser)
NM_001288772.2(PIK3C2G):c.661T>C (p.Trp221Arg)
NM_001288772.2(PIK3C2G):c.679T>A (p.Ser227Thr)
NM_001288772.2(PIK3C2G):c.809A>C (p.Lys270Thr)
NM_001288772.2(PIK3C2G):c.895C>A (p.Gln299Lys)

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