ClinVar Miner

List of variants in gene PIK3CA reported as uncertain significance for not provided

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Total variants: 51
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HGVS dbSNP gnomAD frequency
NM_006218.4(PIK3CA):c.140A>G (p.His47Arg) rs190372148 0.00032
NM_006218.4(PIK3CA):c.2985C>T (p.Ala995=) rs201884756 0.00018
NM_006218.4(PIK3CA):c.1528C>A (p.His510Asn) rs199747934 0.00005
NM_006218.4(PIK3CA):c.178C>A (p.Gln60Lys) rs71310379 0.00004
NM_006218.4(PIK3CA):c.2980C>T (p.His994Tyr) rs1160295534 0.00003
NM_006218.4(PIK3CA):c.341A>G (p.Asn114Ser) rs746860750 0.00002
NM_006218.4(PIK3CA):c.1145G>A (p.Arg382Lys) rs587777794 0.00001
NM_006218.4(PIK3CA):c.2651A>G (p.Lys884Arg) rs1395235750 0.00001
NM_006218.4(PIK3CA):c.436G>A (p.Val146Ile) rs755969956 0.00001
NM_006218.4(PIK3CA):c.954G>A (p.Met318Ile) rs199605762 0.00001
NM_006218.4(PIK3CA):c.112C>T (p.Arg38Cys) rs749415085
NM_006218.4(PIK3CA):c.1153G>A (p.Glu385Lys)
NM_006218.4(PIK3CA):c.11G>C (p.Arg4Pro) rs749956691
NM_006218.4(PIK3CA):c.1201C>T (p.Arg401Ter)
NM_006218.4(PIK3CA):c.1244C>T (p.Ala415Val) rs1576938120
NM_006218.4(PIK3CA):c.1321del (p.Met441fs) rs2108400442
NM_006218.4(PIK3CA):c.1352G>T (p.Gly451Val)
NM_006218.4(PIK3CA):c.1450G>A (p.Val484Ile) rs1004909638
NM_006218.4(PIK3CA):c.148T>C (p.Phe50Leu) rs1064797300
NM_006218.4(PIK3CA):c.1496C>G (p.Ser499Cys) rs1724682773
NM_006218.4(PIK3CA):c.1504C>T (p.Arg502Ter) rs1724683795
NM_006218.4(PIK3CA):c.1615C>T (p.Pro539Ser) rs1724887383
NM_006218.4(PIK3CA):c.1636C>A (p.Gln546Lys) rs121913286
NM_006218.4(PIK3CA):c.1795A>G (p.Met599Val)
NM_006218.4(PIK3CA):c.1807G>A (p.Asp603Asn) rs2108410841
NM_006218.4(PIK3CA):c.1819C>T (p.Pro607Ser) rs2108410891
NM_006218.4(PIK3CA):c.1843G>T (p.Ala615Ser) rs2108410990
NM_006218.4(PIK3CA):c.1955T>C (p.Phe652Ser) rs2108411972
NM_006218.4(PIK3CA):c.2039_2042del (p.Val680fs)
NM_006218.4(PIK3CA):c.2147C>T (p.Thr716Ile) rs2108413765
NM_006218.4(PIK3CA):c.2204T>C (p.Leu735Ser) rs1725027082
NM_006218.4(PIK3CA):c.2221C>T (p.Arg741Ter)
NM_006218.4(PIK3CA):c.2331G>C (p.Arg777Ser) rs771524333
NM_006218.4(PIK3CA):c.2382T>A (p.Phe794Leu) rs2108418129
NM_006218.4(PIK3CA):c.2543T>C (p.Ile848Thr) rs2108422608
NM_006218.4(PIK3CA):c.2618A>G (p.Asn873Ser)
NM_006218.4(PIK3CA):c.2666T>C (p.Ile889Thr) rs1064796841
NM_006218.4(PIK3CA):c.2716G>T (p.Val906Leu)
NM_006218.4(PIK3CA):c.2747G>A (p.Arg916His)
NM_006218.4(PIK3CA):c.2852G>A (p.Arg951His) rs2108425041
NM_006218.4(PIK3CA):c.2924G>A (p.Arg975Lys)
NM_006218.4(PIK3CA):c.29T>C (p.Leu10Pro)
NM_006218.4(PIK3CA):c.3010A>G (p.Met1004Val)
NM_006218.4(PIK3CA):c.3074C>T (p.Thr1025Ile) rs1553826166
NM_006218.4(PIK3CA):c.3091A>G (p.Thr1031Ala)
NM_006218.4(PIK3CA):c.316G>A (p.Gly106Ser)
NM_006218.4(PIK3CA):c.3172A>C (p.Ile1058Leu) rs1576950003
NM_006218.4(PIK3CA):c.325GAA[1] (p.Glu110del) rs1724343994
NM_006218.4(PIK3CA):c.361A>C (p.Ile121Leu)
NM_006218.4(PIK3CA):c.485G>A (p.Arg162Lys) rs1553820511
NM_006218.4(PIK3CA):c.519T>C (p.Ser173=) rs1576932506

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