ClinVar Miner

List of variants in gene PLCG2 reported as uncertain significance for not provided

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Gene type:
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Total variants: 95
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HGVS dbSNP gnomAD frequency
NM_002661.5(PLCG2):c.1444T>C (p.Tyr482His) rs187956469 0.00341
NM_002661.5(PLCG2):c.2393A>G (p.Asn798Ser) rs117077093 0.00061
NM_002661.5(PLCG2):c.77C>T (p.Thr26Met) rs189301790 0.00058
NM_002661.5(PLCG2):c.707C>T (p.Pro236Leu) rs199760975 0.00036
NM_002661.5(PLCG2):c.1695G>C (p.Glu565Asp) rs375590398 0.00015
NM_002661.5(PLCG2):c.1014C>T (p.Ser338=) rs200149635 0.00014
NM_002661.5(PLCG2):c.2383C>G (p.Leu795Val) rs748644186 0.00005
NM_002661.5(PLCG2):c.1559A>G (p.Asp520Gly) rs201391996 0.00004
NM_002661.5(PLCG2):c.502A>G (p.Thr168Ala) rs753974933 0.00004
NM_002661.5(PLCG2):c.594C>G (p.Ser198Arg) rs368738612 0.00004
NM_002661.5(PLCG2):c.2149G>A (p.Val717Ile) rs762414923 0.00003
NM_002661.5(PLCG2):c.2194C>T (p.Arg732Cys) rs369760877 0.00003
NM_002661.5(PLCG2):c.3524T>C (p.Ile1175Thr) rs1265110994 0.00003
NM_002661.5(PLCG2):c.3650A>G (p.Tyr1217Cys) rs373013824 0.00003
NM_002661.5(PLCG2):c.693-6G>C rs755176167 0.00003
NM_002661.5(PLCG2):c.157G>A (p.Ala53Thr) rs532678378 0.00002
NM_002661.5(PLCG2):c.1921C>A (p.His641Asn) rs573799583 0.00002
NM_002661.5(PLCG2):c.2497G>A (p.Glu833Lys) rs753762025 0.00002
NM_002661.5(PLCG2):c.2831A>G (p.Lys944Arg) rs777208551 0.00002
NM_002661.5(PLCG2):c.319A>G (p.Ser107Gly) rs377058251 0.00002
NM_002661.5(PLCG2):c.3380C>G (p.Pro1127Arg) rs369259797 0.00002
NM_002661.5(PLCG2):c.652C>A (p.Leu218Ile) rs551539187 0.00002
NM_002661.5(PLCG2):c.933G>A (p.Met311Ile) rs368534849 0.00002
NM_002661.5(PLCG2):c.1010G>A (p.Arg337Gln) rs1164040767 0.00001
NM_002661.5(PLCG2):c.1501G>T (p.Ala501Ser) rs772234560 0.00001
NM_002661.5(PLCG2):c.1735C>T (p.Arg579Trp) rs1324356186 0.00001
NM_002661.5(PLCG2):c.1855G>A (p.Glu619Lys) rs763166039 0.00001
NM_002661.5(PLCG2):c.1889G>A (p.Arg630Gln) rs771359979 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.2152A>G (p.Ser718Gly) rs767628464 0.00001
NM_002661.5(PLCG2):c.2224C>T (p.Arg742Cys) rs776768909 0.00001
NM_002661.5(PLCG2):c.2296A>C (p.Asn766His) rs955126333 0.00001
NM_002661.5(PLCG2):c.2374C>T (p.Arg792Cys) rs983424200 0.00001
NM_002661.5(PLCG2):c.2488G>A (p.Ala830Thr) rs1166796739 0.00001
NM_002661.5(PLCG2):c.2866C>T (p.Arg956Cys) rs759995209 0.00001
NM_002661.5(PLCG2):c.2912C>T (p.Pro971Leu) rs770381413 0.00001
NM_002661.5(PLCG2):c.3211C>T (p.Arg1071Cys) rs758678624 0.00001
NM_002661.5(PLCG2):c.3308T>C (p.Val1103Ala) rs1008211026 0.00001
NM_002661.5(PLCG2):c.337+2T>C rs866001196 0.00001
NM_002661.5(PLCG2):c.3388G>T (p.Ala1130Ser) rs1003946385 0.00001
NM_002661.5(PLCG2):c.3393T>A (p.Phe1131Leu) rs754374903 0.00001
NM_002661.5(PLCG2):c.3493G>A (p.Val1165Ile) rs372557475 0.00001
NM_002661.5(PLCG2):c.628A>C (p.Met210Leu) rs1367179036 0.00001
NM_002661.5(PLCG2):c.784C>G (p.Leu262Val) rs372563994 0.00001
NM_002661.5(PLCG2):c.922G>A (p.Ala308Thr) rs1382212475 0.00001
NM_002661.5(PLCG2):c.1009C>T (p.Arg337Trp)
NM_002661.5(PLCG2):c.1033T>C (p.Tyr345His) rs1597113444
NM_002661.5(PLCG2):c.1061G>A (p.Arg354His) rs2143609519
NM_002661.5(PLCG2):c.1072+5G>A rs2143609577
NM_002661.5(PLCG2):c.1148_1149inv (p.Asp383Gly)
NM_002661.5(PLCG2):c.12G>C (p.Thr4=)
NM_002661.5(PLCG2):c.1378C>T (p.Pro460Ser)
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.1489G>A (p.Ala497Thr)
NM_002661.5(PLCG2):c.1543G>A (p.Glu515Lys) rs1909439451
NM_002661.5(PLCG2):c.1561A>G (p.Ile521Val) rs1909472222
NM_002661.5(PLCG2):c.1586G>T (p.Gly529Val) rs1013382788
NM_002661.5(PLCG2):c.1766G>A (p.Arg589His) rs761094228
NM_002661.5(PLCG2):c.1923C>G (p.His641Gln) rs374927413
NM_002661.5(PLCG2):c.1934+1G>A rs2143658084
NM_002661.5(PLCG2):c.1971G>C (p.Glu657Asp) rs758439876
NM_002661.5(PLCG2):c.2003C>T (p.Ala668Val)
NM_002661.5(PLCG2):c.2135G>C (p.Ser712Thr) rs2143682705
NM_002661.5(PLCG2):c.2173C>T (p.Leu725Phe) rs1909979385
NM_002661.5(PLCG2):c.2211C>A (p.Pro737=) rs368933697
NM_002661.5(PLCG2):c.2465A>C (p.Asn822Thr) rs746172717
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.2737A>G (p.Lys913Glu)
NM_002661.5(PLCG2):c.289A>G (p.Thr97Ala)
NM_002661.5(PLCG2):c.3285CAA[2] (p.Asn1097del) rs749338323
NM_002661.5(PLCG2):c.3307G>A (p.Val1103Ile)
NM_002661.5(PLCG2):c.3365T>A (p.Phe1122Tyr) rs1057519243
NM_002661.5(PLCG2):c.3379C>G (p.Pro1127Ala) rs762731399
NM_002661.5(PLCG2):c.338-4C>G rs1906784000
NM_002661.5(PLCG2):c.3422T>C (p.Met1141Thr)
NM_002661.5(PLCG2):c.3497C>T (p.Pro1166Leu)
NM_002661.5(PLCG2):c.3527A>G (p.Glu1176Gly)
NM_002661.5(PLCG2):c.3532G>A (p.Ala1178Thr) rs772932697
NM_002661.5(PLCG2):c.3571-3C>G
NM_002661.5(PLCG2):c.3571-7C>A rs1555524600
NM_002661.5(PLCG2):c.3582G>C (p.Glu1194Asp)
NM_002661.5(PLCG2):c.3640C>G (p.Leu1214Val) rs1911585372
NM_002661.5(PLCG2):c.3663G>C (p.Gln1221His) rs1455759195
NM_002661.5(PLCG2):c.3755G>A (p.Arg1252Lys)
NM_002661.5(PLCG2):c.48C>G (p.Ser16Arg) rs752018966
NM_002661.5(PLCG2):c.493G>A (p.Glu165Lys)
NM_002661.5(PLCG2):c.59G>A (p.Arg20Lys) rs1910955135
NM_002661.5(PLCG2):c.656A>G (p.Asp219Gly) rs2143568058
NM_002661.5(PLCG2):c.952C>G (p.Leu318Val) rs1384764686
NM_002661.5(PLCG2):c.956C>G (p.Ser319Cys)
NM_002661.5(PLCG2):c.95G>A (p.Ser32Asn)
NM_002661.5(PLCG2):c.989A>T (p.Tyr330Phe) rs2143609334

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