ClinVar Miner

List of variants in gene PLCG2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_002661.5(PLCG2):c.1565C>G (p.Pro522Arg) rs72824905 0.00491
NM_002661.5(PLCG2):c.3414A>G (p.Glu1138=) rs61755443 0.00247
NM_002661.5(PLCG2):c.987G>A (p.Thr329=) rs200506549 0.00164
NM_002661.5(PLCG2):c.1671G>A (p.Lys557=) rs372347274 0.00111
NM_002661.5(PLCG2):c.923C>T (p.Ala308Val) rs199636472 0.00104
NM_002661.5(PLCG2):c.432-3C>T rs147749022 0.00094
NM_002661.5(PLCG2):c.771T>C (p.His257=) rs369555285 0.00091
NM_002661.5(PLCG2):c.1859C>T (p.Thr620Met) rs147396004 0.00084
NM_002661.5(PLCG2):c.1342C>T (p.Arg448Trp) rs200919414 0.00073
NM_002661.5(PLCG2):c.110C>A (p.Thr37Asn) rs147349332 0.00048
NM_002661.5(PLCG2):c.1107C>T (p.Val369=) rs201652976 0.00041
NM_002661.5(PLCG2):c.1419C>T (p.Asp473=) rs372678135 0.00033
NM_002661.5(PLCG2):c.678C>T (p.Ser226=) rs111553163 0.00021
NM_002661.5(PLCG2):c.171C>T (p.Thr57=) rs374354863 0.00019
NM_002661.5(PLCG2):c.398C>T (p.Ala133Val) rs61755444 0.00016
NM_002661.5(PLCG2):c.2055-7G>A rs373933998 0.00014
NM_002661.5(PLCG2):c.2148C>T (p.Leu716=) rs367677388 0.00014
NM_002661.5(PLCG2):c.1383A>G (p.Arg461=) rs369098550 0.00013
NM_002661.5(PLCG2):c.1569T>A (p.Pro523=) rs199708049 0.00013
NM_002661.5(PLCG2):c.2073G>A (p.Lys691=) rs377223625 0.00009
NM_002661.5(PLCG2):c.3015C>T (p.Cys1005=) rs374501993 0.00009
NM_002661.5(PLCG2):c.2503C>A (p.Leu835Ile) rs186829827 0.00008
NM_002661.5(PLCG2):c.1998C>T (p.Asp666=) rs745784908 0.00006
NM_002661.5(PLCG2):c.313G>A (p.Val105Ile) rs754914807 0.00006
NM_002661.5(PLCG2):c.421A>G (p.Ile141Val) rs554363067 0.00006
NM_002661.5(PLCG2):c.323C>T (p.Thr108Met) rs535715020 0.00005
NM_002661.5(PLCG2):c.1329G>A (p.Ser443=) rs369281824 0.00004
NM_002661.5(PLCG2):c.2580C>T (p.Val860=) rs776770937 0.00004
NM_002661.5(PLCG2):c.2991C>T (p.Tyr997=) rs772244129 0.00004
NM_002661.5(PLCG2):c.502A>G (p.Thr168Ala) rs753974933 0.00004
NM_002661.5(PLCG2):c.97T>C (p.Phe33Leu) rs773040139 0.00004
NM_002661.5(PLCG2):c.1191G>A (p.Ser397=) rs764208800 0.00002
NM_002661.5(PLCG2):c.654C>T (p.Leu218=) rs780503141 0.00002
NM_002661.5(PLCG2):c.72G>C (p.Leu24=) rs756167862 0.00002
NM_002661.5(PLCG2):c.1584T>C (p.Phe528=) rs1278464245 0.00001
NM_002661.5(PLCG2):c.1855G>A (p.Glu619Lys) rs763166039 0.00001
NM_002661.5(PLCG2):c.1995G>A (p.Arg665=) rs781197485 0.00001
NM_002661.5(PLCG2):c.2472C>T (p.Val824=) rs763617895 0.00001
NM_002661.5(PLCG2):c.2582-5C>G rs771695879 0.00001
NM_002661.5(PLCG2):c.3493G>A (p.Val1165Ile) rs372557475 0.00001
NM_002661.5(PLCG2):c.3528G>A (p.Glu1176=) rs1441123083 0.00001
NM_002661.5(PLCG2):c.3575G>C (p.Ser1192Thr) rs761797236 0.00001
NM_002661.5(PLCG2):c.945C>T (p.Asn315=) rs372795428 0.00001
NM_002661.5(PLCG2):c.1035C>T (p.Tyr345=)
NM_002661.5(PLCG2):c.1215C>A (p.Ile405=)
NM_002661.5(PLCG2):c.1386C>T (p.Gly462=) rs759622571
NM_002661.5(PLCG2):c.1392G>C (p.Val464=) rs1183970075
NM_002661.5(PLCG2):c.1446C>T (p.Tyr482=) rs1567525903
NM_002661.5(PLCG2):c.2013C>T (p.Ile671=)
NM_002661.5(PLCG2):c.2202C>T (p.Pro734=) rs200025641
NM_002661.5(PLCG2):c.2232T>C (p.Asn744=)
NM_002661.5(PLCG2):c.2470G>A (p.Val824Ile)
NM_002661.5(PLCG2):c.2514+7C>G rs540522878
NM_002661.5(PLCG2):c.3147C>T (p.Asp1049=)
NM_002661.5(PLCG2):c.3459C>T (p.Tyr1153=) rs773882929
NM_002661.5(PLCG2):c.3489G>A (p.Arg1163=)
NM_002661.5(PLCG2):c.708G>A (p.Pro236=)
NM_002661.5(PLCG2):c.888A>T (p.Ser296=)

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