ClinVar Miner

List of variants in gene PLCG2 reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Gene type:
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Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_002661.5(PLCG2):c.1149C>T (p.Asp383=) rs1143688 0.33340
NM_002661.5(PLCG2):c.802C>T (p.Arg268Trp) rs1143687 0.04677
NM_002661.5(PLCG2):c.2054+7G>A rs138158454 0.02918
NM_002661.5(PLCG2):c.731A>G (p.His244Arg) rs11548656 0.02717
NM_002661.5(PLCG2):c.770A>T (p.His257Leu) rs45443101 0.02615
NM_002661.5(PLCG2):c.1558-18C>T rs113312523 0.01465
NM_002661.5(PLCG2):c.82A>T (p.Met28Leu) rs61749044 0.00973
NM_002661.5(PLCG2):c.3482-3C>T rs74856898 0.00935
NM_002661.5(PLCG2):c.3726C>A (p.Leu1242=) rs76506409 0.00926
NM_002661.5(PLCG2):c.2262C>T (p.Asp754=) rs74032923 0.00884
NM_002661.5(PLCG2):c.1712A>G (p.Asn571Ser) rs75472618 0.00802
NM_002661.5(PLCG2):c.1146T>C (p.Phe382=) rs138637229 0.00731
NM_002661.5(PLCG2):c.2094C>T (p.Asp698=) rs143195637 0.00513
NM_002661.5(PLCG2):c.2542C>T (p.Leu848Phe) rs114618894 0.00510
NM_002661.5(PLCG2):c.1565C>G (p.Pro522Arg) rs72824905 0.00491
NM_002661.5(PLCG2):c.1444T>C (p.Tyr482His) rs187956469 0.00341
NM_002661.5(PLCG2):c.2161G>A (p.Glu721Lys) rs187454354 0.00333
NM_002661.5(PLCG2):c.987G>A (p.Thr329=) rs200506549 0.00164
NM_002661.5(PLCG2):c.2011A>G (p.Ile671Val) rs150833842 0.00157
NM_002661.5(PLCG2):c.1383A>G (p.Arg461=) rs369098550 0.00013
NM_002661.5(PLCG2):c.2259C>T (p.Tyr753=) rs370847174 0.00006
NM_002661.5(PLCG2):c.1935-14G>T rs55645129
NM_002661.5(PLCG2):c.540C>G (p.Ala180=) rs150276286

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