ClinVar Miner

List of variants in gene PLCB1 reported as likely benign by Illumina Laboratory Services, Illumina

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Gene type:
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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_015192.4(PLCB1):c.2565G>A (p.Ala855=) rs2076413 0.24634
NM_015192.4(PLCB1):c.102C>T (p.Asp34=) rs16994453 0.18027
NM_015192.4(PLCB1):c.1251-4T>G rs2076689 0.09450
NM_015192.4(PLCB1):c.*942G>A rs41275594 0.06967
NM_015192.4(PLCB1):c.2082G>A (p.Gly694=) rs3761170 0.05661
NM_015192.4(PLCB1):c.99+8T>C rs6086350 0.04369
NM_015192.4(PLCB1):c.*1798T>G rs73089700 0.03493
NM_015192.4(PLCB1):c.*1670C>T rs41275598 0.03141
NM_015192.4(PLCB1):c.*97A>G rs41275590 0.02442
NM_015192.4(PLCB1):c.*749G>C rs16995375 0.01704
NM_182734.2(PLCB1):c.*3300C>A rs114229570 0.01610
NM_015192.4(PLCB1):c.924A>G (p.Ser308=) rs6056003 0.01487
NM_015192.4(PLCB1):c.178-15G>A rs6055775 0.01196
NM_015192.4(PLCB1):c.*855G>A rs115731722 0.00722
NM_015192.4(PLCB1):c.*1538G>T rs116163517 0.00719
NM_015192.4(PLCB1):c.1167+7T>C rs45466294 0.00492
NM_015192.4(PLCB1):c.2673T>G (p.Pro891=) rs142813933 0.00260
NM_015192.4(PLCB1):c.3116T>C (p.Ile1039Thr) rs75820839 0.00251
NM_015192.4(PLCB1):c.*1954_*1957del rs78940282
NM_015192.4(PLCB1):c.*2096GAA[2] rs140743311
NM_015192.4(PLCB1):c.*378_*380dup rs147873196
NM_015192.4(PLCB1):c.*93del rs146432082

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