ClinVar Miner

List of variants in gene PLCG2 studied for not specified

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Gene type:
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Total variants: 70
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HGVS dbSNP gnomAD frequency
NM_002661.5(PLCG2):c.2235+99A>G rs12448152 0.99979
NM_002661.5(PLCG2):c.2055-8T>C rs12448130 0.99106
NM_002661.5(PLCG2):c.3314-23C>A rs4405546 0.91524
NM_002661.5(PLCG2):c.1467+38G>C rs4435248 0.75887
NM_002661.5(PLCG2):c.431+37G>C rs4341734 0.74949
NM_002661.5(PLCG2):c.1467+125C>T rs4264387 0.74061
NM_002661.5(PLCG2):c.1497C>T (p.Ala499=) rs1143689 0.73561
NM_002661.5(PLCG2):c.174T>C (p.Ala58=) rs1143685 0.68990
NM_002661.5(PLCG2):c.1193+1830T>C rs8053636 0.66112
NM_002661.5(PLCG2):c.432-13T>A rs4888183 0.55511
NM_002661.5(PLCG2):c.2417+104T>G rs16955980 0.54861
NM_002661.5(PLCG2):c.480-22A>G rs12445580 0.54715
NM_002661.5(PLCG2):c.565-82C>A rs35039495 0.54617
NM_002661.5(PLCG2):c.565-83_565-82insT rs146168517 0.54587
NM_002661.5(PLCG2):c.431+81_431+83del rs5818357 0.50986
NM_002661.5(PLCG2):c.2236-14C>G rs12446127 0.48966
NM_002661.5(PLCG2):c.3199-123T>G rs12596299 0.45725
NM_002661.5(PLCG2):c.-47-62C>G rs4354929 0.45184
NM_002661.5(PLCG2):c.3198+149T>C rs4611451 0.43273
NM_002661.5(PLCG2):c.2054+102C>T rs4243222 0.41556
NM_002661.5(PLCG2):c.3093T>C (p.Asn1031=) rs1071644 0.39075
NM_002661.5(PLCG2):c.3199-117A>C rs4888192 0.37635
NM_002661.5(PLCG2):c.1193+1871A>G rs8049305 0.34720
NM_002661.5(PLCG2):c.1149C>T (p.Asp383=) rs1143688 0.33340
NM_002661.5(PLCG2):c.692+25C>T rs11865395 0.28480
NM_002661.5(PLCG2):c.194-92A>C rs4072830 0.28423
NM_002661.5(PLCG2):c.297A>G (p.Leu99=) rs1143686 0.26621
NM_002661.5(PLCG2):c.194-111T>C rs4522412 0.26000
NM_002661.5(PLCG2):c.194-146A>G rs4072831 0.25980
NM_002661.5(PLCG2):c.1557+65C>T rs71400183 0.20860
NM_002661.5(PLCG2):c.564+87G>A rs4889419 0.19338
NM_002661.5(PLCG2):c.480-89del rs77062887 0.14061
NM_002661.5(PLCG2):c.194-72G>C rs34028338 0.09629
NM_002661.5(PLCG2):c.1188C>G (p.Thr396=) rs13333716 0.06533
NM_002661.5(PLCG2):c.3314-55T>C rs11150425 0.05784
NM_002661.5(PLCG2):c.802C>T (p.Arg268Trp) rs1143687 0.04551
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.82A>T (p.Met28Leu) rs61749044 0.00973
NM_002661.5(PLCG2):c.2262C>T (p.Asp754=) rs74032923 0.00884
NM_002661.5(PLCG2):c.3482-3C>T rs74856898 0.00883
NM_002661.5(PLCG2):c.1712A>G (p.Asn571Ser) rs75472618 0.00802
NM_002661.5(PLCG2):c.1146T>C (p.Phe382=) rs138637229 0.00682
NM_002661.5(PLCG2):c.2094C>T (p.Asp698=) rs143195637 0.00513
NM_002661.5(PLCG2):c.77C>T (p.Thr26Met) rs189301790 0.00060
NM_002661.5(PLCG2):c.171C>T (p.Thr57=) rs374354863 0.00019
NM_002661.5(PLCG2):c.2211C>T (p.Pro737=) rs368933697 0.00019
NM_002661.5(PLCG2):c.1116T>C (p.His372=) rs369732261 0.00013
NM_002661.5(PLCG2):c.2312A>G (p.Gln771Arg) rs201803492 0.00013
NM_002661.5(PLCG2):c.2259C>T (p.Tyr753=) rs370847174 0.00006
NM_002661.5(PLCG2):c.2577C>T (p.Asn859=) rs747043855 0.00006
NM_002661.5(PLCG2):c.502A>G (p.Thr168Ala) rs753974933 0.00004
NM_002661.5(PLCG2):c.3657A>T (p.Thr1219=) rs201318091 0.00003
NM_002661.5(PLCG2):c.1501G>T (p.Ala501Ser) rs772234560 0.00001
NM_002661.5(PLCG2):c.2201C>T (p.Pro734Leu) rs199516791 0.00001
NM_002661.5(PLCG2):c.1194-19C>T
NM_002661.5(PLCG2):c.193+33G>A rs4294811
NM_002661.5(PLCG2):c.2055-8_2055-7inv
NM_002661.5(PLCG2):c.2236-19T>G rs2143686815
NM_002661.5(PLCG2):c.2515-92A>C rs4366702
NM_002661.5(PLCG2):c.3165C>T (p.Ser1055=) rs2507759987
NM_002661.5(PLCG2):c.3198+169G>A rs4369659
NM_002661.5(PLCG2):c.3198+74A>G rs4258608
NM_002661.5(PLCG2):c.337+45G>C rs4072828
NM_002661.5(PLCG2):c.431+87A>C rs5016604
NM_002661.5(PLCG2):c.565-22del rs34761601
NM_002661.5(PLCG2):c.565-82delinsTA rs367901037
NM_002661.5(PLCG2):c.648+134T>C rs7192509
NM_002661.5(PLCG2):c.692+61A>C rs41305761

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