ClinVar Miner

List of variants in gene PLCG2 reported by Fulgent Genetics, Fulgent Genetics

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Gene type:
ClinVar version:
Total variants: 177
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HGVS dbSNP gnomAD frequency
NM_002661.5(PLCG2):c.2236-14C>G rs12446127 0.48966
NM_002661.5(PLCG2):c.1558-18C>T rs113312523 0.01465
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.2094C>T (p.Asp698=) rs143195637 0.00513
NM_002661.5(PLCG2):c.2355C>T (p.Ser785=) rs185307548 0.00307
NM_002661.5(PLCG2):c.600A>G (p.Glu200=) rs142140333 0.00294
NM_002661.5(PLCG2):c.1557+6G>C rs139565830 0.00235
NM_002661.5(PLCG2):c.1050C>A (p.Arg350=) rs185739725 0.00212
NM_002661.5(PLCG2):c.3573G>A (p.Glu1191=) rs201682723 0.00128
NM_002661.5(PLCG2):c.1671G>A (p.Lys557=) rs372347274 0.00111
NM_002661.5(PLCG2):c.432-3C>T rs147749022 0.00094
NM_002661.5(PLCG2):c.3112C>T (p.Leu1038=) rs200813182 0.00067
NM_002661.5(PLCG2):c.57G>A (p.Lys19=) rs369542354 0.00055
NM_002661.5(PLCG2):c.110C>A (p.Thr37Asn) rs147349332 0.00048
NM_002661.5(PLCG2):c.2054+11G>C rs372245323 0.00041
NM_002661.5(PLCG2):c.1959C>T (p.Arg653=) rs117835631 0.00035
NM_002661.5(PLCG2):c.1419C>T (p.Asp473=) rs372678135 0.00033
NM_002661.5(PLCG2):c.3198+20C>G rs141049260 0.00032
NM_002661.5(PLCG2):c.2739+8C>A rs201659233 0.00030
NM_002661.5(PLCG2):c.2655G>A (p.Pro885=) rs187441573 0.00029
NM_002661.5(PLCG2):c.648+12C>G rs145838332 0.00027
NM_002661.5(PLCG2):c.2260G>C (p.Asp754His) rs190001915 0.00026
NM_002661.5(PLCG2):c.766-13T>G rs115570507 0.00022
NM_002661.5(PLCG2):c.2427A>G (p.Gly809=) rs200844173 0.00021
NM_002661.5(PLCG2):c.406G>A (p.Ala136Thr) rs367885048 0.00021
NM_002661.5(PLCG2):c.480-15C>T rs368147709 0.00021
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.1923C>T (p.His641=) rs374927413 0.00016
NM_002661.5(PLCG2):c.2940G>A (p.Lys980=) rs376216756 0.00016
NM_002661.5(PLCG2):c.581A>T (p.Lys194Ile) rs372054297 0.00016
NM_002661.5(PLCG2):c.1695G>C (p.Glu565Asp) rs375590398 0.00015
NM_002661.5(PLCG2):c.2148C>T (p.Leu716=) rs367677388 0.00014
NM_002661.5(PLCG2):c.510G>T (p.Leu170Phe) rs759598100 0.00014
NM_002661.5(PLCG2):c.1116T>C (p.His372=) rs369732261 0.00013
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.2913C>T (p.Pro971=) rs377752384 0.00013
NM_002661.5(PLCG2):c.1557+14C>G rs372814853 0.00012
NM_002661.5(PLCG2):c.3396G>A (p.Leu1132=) rs201475640 0.00011
NM_002661.5(PLCG2):c.2503C>A (p.Leu835Ile) rs186829827 0.00008
NM_002661.5(PLCG2):c.2581+10C>G rs367866295 0.00008
NM_002661.5(PLCG2):c.2055-10C>A rs747616797 0.00007
NM_002661.5(PLCG2):c.2236-15_2236-14insG rs768770205 0.00007
NM_002661.5(PLCG2):c.3516C>T (p.Ser1172=) rs773778524 0.00007
NM_002661.5(PLCG2):c.114C>T (p.Pro38=) rs750924322 0.00006
NM_002661.5(PLCG2):c.1558-8C>T rs371117206 0.00006
NM_002661.5(PLCG2):c.1629C>T (p.Ala543=) rs374641731 0.00006
NM_002661.5(PLCG2):c.1881C>T (p.Phe627=) rs754739394 0.00006
NM_002661.5(PLCG2):c.1998C>T (p.Asp666=) rs745784908 0.00006
NM_002661.5(PLCG2):c.2259C>T (p.Tyr753=) rs370847174 0.00006
NM_002661.5(PLCG2):c.2331G>A (p.Leu777=) rs372491825 0.00006
NM_002661.5(PLCG2):c.2577C>T (p.Asn859=) rs747043855 0.00006
NM_002661.5(PLCG2):c.313G>A (p.Val105Ile) rs754914807 0.00006
NM_002661.5(PLCG2):c.32C>T (p.Ala11Val) rs753458249 0.00006
NM_002661.5(PLCG2):c.3336C>T (p.Ile1112=) rs193128632 0.00006
NM_002661.5(PLCG2):c.3374A>G (p.Tyr1125Cys) rs374877793 0.00006
NM_002661.5(PLCG2):c.3682C>T (p.Arg1228Trp) rs202108152 0.00006
NM_002661.5(PLCG2):c.421A>G (p.Ile141Val) rs554363067 0.00006
NM_002661.5(PLCG2):c.487C>T (p.Leu163Phe) rs375598204 0.00006
NM_002661.5(PLCG2):c.1073-15C>T rs371214101 0.00005
NM_002661.5(PLCG2):c.1464C>T (p.Asp488=) rs777149251 0.00005
NM_002661.5(PLCG2):c.2383C>G (p.Leu795Val) rs748644186 0.00005
NM_002661.5(PLCG2):c.323C>T (p.Thr108Met) rs535715020 0.00005
NM_002661.5(PLCG2):c.3423G>A (p.Met1141Ile) rs552036893 0.00005
NM_002661.5(PLCG2):c.3571-10C>T rs376240742 0.00005
NM_002661.5(PLCG2):c.407C>T (p.Ala136Val) rs777990663 0.00005
NM_002661.5(PLCG2):c.485G>C (p.Ser162Thr) rs142022471 0.00005
NM_002661.5(PLCG2):c.925G>A (p.Val309Met) rs768664050 0.00005
NM_002661.5(PLCG2):c.1073-17C>T rs572040225 0.00004
NM_002661.5(PLCG2):c.1387G>A (p.Asp463Asn) rs752906992 0.00004
NM_002661.5(PLCG2):c.1558-4C>A rs1325379831 0.00004
NM_002661.5(PLCG2):c.1559A>G (p.Asp520Gly) rs201391996 0.00004
NM_002661.5(PLCG2):c.183C>T (p.Ile61=) rs553657822 0.00004
NM_002661.5(PLCG2):c.2055-20C>A rs563045009 0.00004
NM_002661.5(PLCG2):c.2164A>G (p.Lys722Glu) rs761399374 0.00004
NM_002661.5(PLCG2):c.2301G>A (p.Pro767=) rs374390386 0.00004
NM_002661.5(PLCG2):c.2307+4C>T rs745912221 0.00004
NM_002661.5(PLCG2):c.2496C>T (p.Phe832=) rs766166854 0.00004
NM_002661.5(PLCG2):c.2578G>A (p.Val860Ile) rs370187601 0.00004
NM_002661.5(PLCG2):c.3289A>G (p.Asn1097Asp) rs771322094 0.00004
NM_002661.5(PLCG2):c.3343C>T (p.Pro1115Ser) rs372606303 0.00004
NM_002661.5(PLCG2):c.3420T>C (p.Asp1140=) rs746749620 0.00004
NM_002661.5(PLCG2):c.3492C>T (p.Ser1164=) rs187113357 0.00004
NM_002661.5(PLCG2):c.3780C>G (p.Asn1260Lys) rs758825034 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.1194-16C>A rs778184999 0.00003
NM_002661.5(PLCG2):c.147G>A (p.Thr49=) rs969768555 0.00003
NM_002661.5(PLCG2):c.2235+3A>G rs544435013 0.00003
NM_002661.5(PLCG2):c.2245A>G (p.Ile749Val) rs761876435 0.00003
NM_002661.5(PLCG2):c.2522A>G (p.Glu841Gly) rs756855626 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.438G>A (p.Leu146=) rs976068042 0.00003
NM_002661.5(PLCG2):c.766-7T>C rs1055824436 0.00003
NM_002661.5(PLCG2):c.127G>A (p.Val43Ile) rs370352962 0.00002
NM_002661.5(PLCG2):c.1437G>A (p.Gly479=) rs755597785 0.00002
NM_002661.5(PLCG2):c.1733+11C>T rs750585339 0.00002
NM_002661.5(PLCG2):c.1778A>G (p.Glu593Gly) rs776632754 0.00002
NM_002661.5(PLCG2):c.1935-4G>A rs762488045 0.00002
NM_002661.5(PLCG2):c.246C>T (p.Phe82=) rs771764012 0.00002
NM_002661.5(PLCG2):c.2740-13G>A rs1280371637 0.00002
NM_002661.5(PLCG2):c.3072T>C (p.Asn1024=) rs755927399 0.00002
NM_002661.5(PLCG2):c.3199-16C>T rs201410855 0.00002
NM_002661.5(PLCG2):c.3380C>G (p.Pro1127Arg) rs369259797 0.00002
NM_002661.5(PLCG2):c.3458A>G (p.Tyr1153Cys) rs146175110 0.00002
NM_002661.5(PLCG2):c.3544G>A (p.Val1182Ile) rs759887275 0.00002
NM_002661.5(PLCG2):c.3742A>C (p.Lys1248Gln) rs867313284 0.00002
NM_002661.5(PLCG2):c.3755G>C (p.Arg1252Thr) rs748492148 0.00002
NM_002661.5(PLCG2):c.1176C>T (p.His392=) rs773286721 0.00001
NM_002661.5(PLCG2):c.1212C>T (p.Ser404=) rs1405057614 0.00001
NM_002661.5(PLCG2):c.1236G>A (p.Glu412=) rs372240617 0.00001
NM_002661.5(PLCG2):c.1301C>T (p.Thr434Met) rs757785924 0.00001
NM_002661.5(PLCG2):c.1306G>A (p.Ala436Thr) rs1225918799 0.00001
NM_002661.5(PLCG2):c.1362+8C>A rs372538067 0.00001
NM_002661.5(PLCG2):c.1467+3G>A rs759974672 0.00001
NM_002661.5(PLCG2):c.1567C>G (p.Pro523Ala) rs574435526 0.00001
NM_002661.5(PLCG2):c.1634A>G (p.Lys545Arg) rs1555519355 0.00001
NM_002661.5(PLCG2):c.1745G>A (p.Arg582Gln) rs200325678 0.00001
NM_002661.5(PLCG2):c.1783G>A (p.Gly595Arg) rs758138167 0.00001
NM_002661.5(PLCG2):c.1855G>A (p.Glu619Lys) rs763166039 0.00001
NM_002661.5(PLCG2):c.1934+8T>G rs780081424 0.00001
NM_002661.5(PLCG2):c.2032G>A (p.Asp678Asn) rs541071022 0.00001
NM_002661.5(PLCG2):c.2067G>A (p.Lys689=) rs1369861469 0.00001
NM_002661.5(PLCG2):c.2102A>G (p.His701Arg) rs777219718 0.00001
NM_002661.5(PLCG2):c.2224C>T (p.Arg742Cys) rs776768909 0.00001
NM_002661.5(PLCG2):c.2263G>A (p.Val755Ile) rs758623675 0.00001
NM_002661.5(PLCG2):c.2296A>C (p.Asn766His) rs955126333 0.00001
NM_002661.5(PLCG2):c.2399C>G (p.Ser800Cys) rs769337881 0.00001
NM_002661.5(PLCG2):c.2581+5G>A rs769466948 0.00001
NM_002661.5(PLCG2):c.2739+19G>A rs776050949 0.00001
NM_002661.5(PLCG2):c.2828C>G (p.Thr943Ser) rs771302628 0.00001
NM_002661.5(PLCG2):c.2867G>A (p.Arg956His) rs376030995 0.00001
NM_002661.5(PLCG2):c.2912C>T (p.Pro971Leu) rs770381413 0.00001
NM_002661.5(PLCG2):c.3002G>A (p.Arg1001His) rs752209691 0.00001
NM_002661.5(PLCG2):c.3034C>T (p.Leu1012Phe) rs1597143704 0.00001
NM_002661.5(PLCG2):c.304A>G (p.Thr102Ala) rs991965495 0.00001
NM_002661.5(PLCG2):c.3097C>T (p.Arg1033Cys) rs376667295 0.00001
NM_002661.5(PLCG2):c.3098G>A (p.Arg1033His) rs760293225 0.00001
NM_002661.5(PLCG2):c.3109G>A (p.Val1037Ile) rs373561919 0.00001
NM_002661.5(PLCG2):c.3388G>T (p.Ala1130Ser) rs1003946385 0.00001
NM_002661.5(PLCG2):c.3493G>A (p.Val1165Ile) rs372557475 0.00001
NM_002661.5(PLCG2):c.3504G>T (p.Lys1168Asn) rs1447212251 0.00001
NM_002661.5(PLCG2):c.3721C>T (p.Gln1241Ter) rs1406944158 0.00001
NM_002661.5(PLCG2):c.3750C>G (p.Asn1250Lys) rs1911592073 0.00001
NM_002661.5(PLCG2):c.547C>T (p.Leu183Phe) rs772451566 0.00001
NM_002661.5(PLCG2):c.591C>T (p.Leu197=) rs1440994305 0.00001
NM_002661.5(PLCG2):c.628A>C (p.Met210Leu) rs1367179036 0.00001
NM_002661.5(PLCG2):c.679G>A (p.Val227Met) rs769793664 0.00001
NM_002661.5(PLCG2):c.692+7C>T rs773842088 0.00001
NM_002661.5(PLCG2):c.784C>G (p.Leu262Val) rs372563994 0.00001
NM_002661.5(PLCG2):c.839C>G (p.Thr280Ser) rs757316414 0.00001
NM_002661.5(PLCG2):c.843T>C (p.Ala281=) rs755732530 0.00001
NM_002661.5(PLCG2):c.875C>T (p.Thr292Met) rs772003833 0.00001
NM_002661.5(PLCG2):c.922G>A (p.Ala308Thr) rs1382212475 0.00001
NM_002661.5(PLCG2):c.1420G>A (p.Glu474Lys) rs867345397
NM_002661.5(PLCG2):c.2055-8_2055-7inv
NM_002661.5(PLCG2):c.2090G>A (p.Arg697Gln) rs767717794
NM_002661.5(PLCG2):c.2236-14C>T rs12446127
NM_002661.5(PLCG2):c.3053-8C>A rs1267501546
NM_002661.5(PLCG2):c.3075C>G (p.His1025Gln) rs368241065
NM_002661.5(PLCG2):c.3192A>C (p.Thr1064=) rs200366770
NM_002661.5(PLCG2):c.324G>C (p.Thr108=) rs189282309
NM_002661.5(PLCG2):c.3285CAA[2] (p.Asn1097del) rs749338323
NM_002661.5(PLCG2):c.3379C>G (p.Pro1127Ala) rs762731399
NM_002661.5(PLCG2):c.3747C>G (p.Cys1249Trp) rs1197295448
NM_002661.5(PLCG2):c.3756-20T>A rs762802134
NM_002661.5(PLCG2):c.48C>G (p.Ser16Arg) rs752018966
NM_002661.5(PLCG2):c.540C>G (p.Ala180=) rs150276286
NM_002661.5(PLCG2):c.540C>T (p.Ala180=) rs150276286
NM_002661.5(PLCG2):c.852C>A (p.Phe284Leu) rs190687540
NM_002661.5(PLCG2):c.906G>C (p.Trp302Cys) rs1908633748
NM_002661.5(PLCG2):c.942G>A (p.Met314Ile) rs1555517092

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