ClinVar Miner

List of variants in gene PLCG2 reported as uncertain significance by Ambry Genetics

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Total variants: 32
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HGVS dbSNP gnomAD frequency
NM_002661.5(PLCG2):c.88G>T (p.Val30Leu) rs372502550 0.00031
NM_002661.5(PLCG2):c.2036C>G (p.Ser679Cys) rs374768937 0.00022
NM_002661.5(PLCG2):c.421A>G (p.Ile141Val) rs554363067 0.00006
NM_002661.5(PLCG2):c.485G>C (p.Ser162Thr) rs142022471 0.00005
NM_002661.5(PLCG2):c.2494T>C (p.Phe832Leu) rs368530152 0.00002
NM_002661.5(PLCG2):c.2488G>A (p.Ala830Thr) rs1166796739 0.00001
NM_002661.5(PLCG2):c.2912C>T (p.Pro971Leu) rs770381413 0.00001
NM_002661.5(PLCG2):c.292A>G (p.Ile98Val) rs1273224701 0.00001
NM_002661.5(PLCG2):c.3149C>T (p.Pro1050Leu) rs372812991 0.00001
NM_002661.5(PLCG2):c.3239T>A (p.Ile1080Asn) rs747179742 0.00001
NM_002661.5(PLCG2):c.784C>G (p.Leu262Val) rs372563994 0.00001
NM_002661.5(PLCG2):c.858T>G (p.Phe286Leu) rs962152757 0.00001
NM_002661.5(PLCG2):c.1086C>G (p.Asp362Glu) rs375876385
NM_002661.5(PLCG2):c.1334G>C (p.Ser445Thr)
NM_002661.5(PLCG2):c.13G>T (p.Val5Phe)
NM_002661.5(PLCG2):c.1586G>T (p.Gly529Val) rs1013382788
NM_002661.5(PLCG2):c.1775T>G (p.Met592Arg) rs1555519696
NM_002661.5(PLCG2):c.1813C>G (p.Leu605Val)
NM_002661.5(PLCG2):c.1853G>T (p.Arg618Leu)
NM_002661.5(PLCG2):c.2414G>T (p.Gly805Val)
NM_002661.5(PLCG2):c.254C>G (p.Ala85Gly)
NM_002661.5(PLCG2):c.2711G>A (p.Arg904Gln)
NM_002661.5(PLCG2):c.334G>T (p.Ala112Ser)
NM_002661.5(PLCG2):c.3602G>A (p.Arg1201His)
NM_002661.5(PLCG2):c.3709G>C (p.Val1237Leu)
NM_002661.5(PLCG2):c.3760A>G (p.Arg1254Gly)
NM_002661.5(PLCG2):c.755A>G (p.His252Arg)
NM_002661.5(PLCG2):c.829A>G (p.Met277Val)
NM_002661.5(PLCG2):c.841G>A (p.Ala281Thr)
NM_002661.5(PLCG2):c.956C>G (p.Ser319Cys)
NM_002661.5(PLCG2):c.958C>T (p.His320Tyr)
NM_002661.5(PLCG2):c.991C>G (p.Leu331Val) rs2143609348

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