ClinVar Miner

List of variants in gene PLCG2 reported as uncertain significance by GeneDx

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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_002661.5(PLCG2):c.502A>G (p.Thr168Ala) rs753974933 0.00004
NM_002661.5(PLCG2):c.1855G>A (p.Glu619Lys) rs763166039 0.00001
NM_002661.5(PLCG2):c.2080C>T (p.Arg694Cys) rs764736362 0.00001
NM_002661.5(PLCG2):c.2102A>G (p.His701Arg) rs777219718 0.00001
NM_002661.5(PLCG2):c.2831A>G (p.Lys944Arg) rs777208551 0.00001
NM_002661.5(PLCG2):c.2912C>T (p.Pro971Leu) rs770381413 0.00001
NM_002661.5(PLCG2):c.628A>C (p.Met210Leu) rs1367179036 0.00001
NM_002661.5(PLCG2):c.922G>A (p.Ala308Thr) rs1382212475 0.00001
NM_002661.5(PLCG2):c.1009C>T (p.Arg337Trp) rs1327269467
NM_002661.5(PLCG2):c.12G>C (p.Thr4=) rs376949064
NM_002661.5(PLCG2):c.1381_1382delinsTT (p.Arg461Leu) rs1597121708
NM_002661.5(PLCG2):c.1446C>G (p.Tyr482Ter) rs1567525903
NM_002661.5(PLCG2):c.1537A>G (p.Met513Val) rs764836810
NM_002661.5(PLCG2):c.1543G>A (p.Glu515Lys) rs1909439451
NM_002661.5(PLCG2):c.2135G>C (p.Ser712Thr) rs2143682705
NM_002661.5(PLCG2):c.2323A>G (p.Lys775Glu)
NM_002661.5(PLCG2):c.2340C>G (p.Tyr780Ter)
NM_002661.5(PLCG2):c.2604C>A (p.Asn868Lys) rs1131691537
NM_002661.5(PLCG2):c.2661G>T (p.Glu887Asp) rs201601618
NM_002661.5(PLCG2):c.3571-7C>A rs1555524600
NM_002661.5(PLCG2):c.3582G>C (p.Glu1194Asp) rs1911582997
NM_002661.5(PLCG2):c.3745T>G (p.Cys1249Gly)
NM_002661.5(PLCG2):c.493G>A (p.Glu165Lys) rs542611829
NM_002661.5(PLCG2):c.989A>T (p.Tyr330Phe) rs2143609334

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