ClinVar Miner

List of variants in gene PLEC reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 100
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HGVS dbSNP
GRCh37/hg19 8q24.3(chr8:144990528-144992862)x1
GRCh37/hg19 8q24.3(chr8:144992269-144992953)x1
GRCh37/hg19 8q24.3(chr8:144994331-145004376)x1
GRCh37/hg19 8q24.3(chr8:144995807-145004376)x1
NC_000008.11:g.143938997dup rs143293850
NM_000445.5(PLEC):c.10139G>C (p.Gly3380Ala) rs35261863
NM_000445.5(PLEC):c.1027-33C>G rs6994460
NM_000445.5(PLEC):c.10383C>A (p.Thr3461=) rs199879193
NM_000445.5(PLEC):c.10693T>C (p.Leu3565=) rs6992333
NM_000445.5(PLEC):c.11001C>T (p.Tyr3667=) rs28455570
NM_000445.5(PLEC):c.11170C>T (p.Leu3724=) rs17062686
NM_000445.5(PLEC):c.1123-93G>A rs11782433
NM_000445.5(PLEC):c.11801C>T (p.Thr3934Met) rs78461695
NM_000445.5(PLEC):c.11967A>G (p.Thr3989=) rs6558406
NM_000445.5(PLEC):c.1250+43T>A rs11783772
NM_000445.5(PLEC):c.1251-83G>T rs11782331
NM_000445.5(PLEC):c.12723C>T (p.Ile4241=) rs111227648
NM_000445.5(PLEC):c.12898C>T (p.Pro4300Ser) rs202040785
NM_000445.5(PLEC):c.1317G>A (p.Leu439=) rs190791617
NM_000445.5(PLEC):c.13329G>A (p.Thr4443=) rs115621402
NM_000445.5(PLEC):c.1344+177T>C rs11136337
NM_000445.5(PLEC):c.1344+219C>T rs6989119
NM_000445.5(PLEC):c.13656G>A (p.Ser4552=) rs549882307
NM_000445.5(PLEC):c.1787G>A (p.Arg596Gln) rs3135103
NM_000445.5(PLEC):c.194-1033G>C rs4073081
NM_000445.5(PLEC):c.194-15012C>G rs61467040
NM_000445.5(PLEC):c.194-15138C>T rs147713970
NM_000445.5(PLEC):c.194-455C>A rs11784501
NM_000445.5(PLEC):c.194-485G>A rs11136339
NM_000445.5(PLEC):c.194-6217G>T rs73377226
NM_000445.5(PLEC):c.194-655A>G rs191308779
NM_000445.5(PLEC):c.194-915C>T rs11784619
NM_000445.5(PLEC):c.2386-240A>G rs10107388
NM_000445.5(PLEC):c.255+22G>C rs7823393
NM_000445.5(PLEC):c.256-58T>C rs11136338
NM_000445.5(PLEC):c.2632G>A (p.Val878Met) rs200647397
NM_000445.5(PLEC):c.26G>A (p.Arg9Gln) rs138978753
NM_000445.5(PLEC):c.3004+37C>T rs11136335
NM_000445.5(PLEC):c.3342-123T>C rs11993233
NM_000445.5(PLEC):c.345+113C>T rs13439519
NM_000445.5(PLEC):c.3838-9A>G rs57461687
NM_000445.5(PLEC):c.3921+48A>G rs11782890
NM_000445.5(PLEC):c.3922-51A>T rs55984967
NM_000445.5(PLEC):c.3922-57C>T rs113473982
NM_000445.5(PLEC):c.3922-62A>G rs55812715
NM_000445.5(PLEC):c.3950A>G (p.Lys1317Arg) rs200895043
NM_000445.5(PLEC):c.4125+143C>T rs7017789
NM_000445.5(PLEC):c.4125+212C>T rs7017644
NM_000445.5(PLEC):c.4125+54T>C rs56401829
NM_000445.5(PLEC):c.4126-169C>T rs7016860
NM_000445.5(PLEC):c.4164G>A (p.Arg1388=) rs377619355
NM_000445.5(PLEC):c.4557G>A (p.Ala1519=) rs55646585
NM_000445.5(PLEC):c.459T>C (p.Ala153=) rs6993938
NM_000445.5(PLEC):c.4954G>A (p.Glu1652Lys) rs187338487
NM_000445.5(PLEC):c.517-123T>C rs6988767
NM_000445.5(PLEC):c.517-153G>A rs58958846
NM_000445.5(PLEC):c.517-163A>G rs58905421
NM_000445.5(PLEC):c.5754C>T (p.Ile1918=) rs191863619
NM_000445.5(PLEC):c.6150C>G (p.Arg2050=) rs376365984
NM_000445.5(PLEC):c.6489G>A (p.Glu2163=) rs200444977
NM_000445.5(PLEC):c.6810C>T (p.Leu2270=) rs368880818
NM_000445.5(PLEC):c.683+130C>T rs73377218
NM_000445.5(PLEC):c.684-112T>G rs6983908
NM_000445.5(PLEC):c.684-129T>C rs11784762
NM_000445.5(PLEC):c.7506+37C>T rs11786934
NM_000445.5(PLEC):c.7507-35C>T rs11786903
NM_000445.5(PLEC):c.7911G>A (p.Ala2637=) rs376112916
NM_000445.5(PLEC):c.8106C>T (p.Gly2702=) rs35139934
NM_000445.5(PLEC):c.8694C>T (p.Cys2898=) rs35821434
NM_000445.5(PLEC):c.8706C>T (p.Pro2902=) rs183401234
NM_000445.5(PLEC):c.8901C>G (p.Asp2967Glu) rs58308209
NM_000445.5(PLEC):c.9414G>A (p.Gly3138=) rs188739870
NM_000445.5(PLEC):c.9432C>T (p.Phe3144=) rs200895343
NM_201378.4(PLEC):c.10717C>T (p.Leu3573=) rs200006106
NM_201378.4(PLEC):c.12742G>A (p.Val4248Ile) rs142946078
NM_201378.4(PLEC):c.130A>G (p.Lys44Glu) rs199985628
NM_201378.4(PLEC):c.13107C>T (p.Ala4369=) rs199719299
NM_201378.4(PLEC):c.13428C>T (p.Arg4476=) rs531535217
NM_201378.4(PLEC):c.1376+40C>T rs115492306
NM_201378.4(PLEC):c.2262+252A>G rs62522556
NM_201378.4(PLEC):c.2262+261A>G rs73715561
NM_201378.4(PLEC):c.2436C>T (p.Asp812=) rs202135215
NM_201378.4(PLEC):c.2493C>T (p.Ser831=) rs199721954
NM_201378.4(PLEC):c.3219-271G>C rs62522555
NM_201378.4(PLEC):c.4002+62A>G rs139985577
NM_201378.4(PLEC):c.4003-269G>A rs6993953
NM_201378.4(PLEC):c.4324G>A (p.Val1442Met) rs186848953
NM_201378.4(PLEC):c.4514C>T (p.Ser1505Leu) rs182120395
NM_201378.4(PLEC):c.4556G>A (p.Arg1519Gln) rs201430180
NM_201378.4(PLEC):c.5435G>A (p.Arg1812Gln) rs147838690
NM_201378.4(PLEC):c.6128C>T (p.Ala2043Val) rs7002002
NM_201378.4(PLEC):c.71-1089G>A rs4073082
NM_201378.4(PLEC):c.71-1128_71-1127insCT rs5895792
NM_201378.4(PLEC):c.71-12438G>A rs73715570
NM_201378.4(PLEC):c.7225G>A (p.Ala2409Thr) rs193257576
NM_201378.4(PLEC):c.812G>A (p.Arg271Gln) rs188076386
NM_201378.4(PLEC):c.8388C>G (p.Ile2796Met) rs62641758
NM_201378.4(PLEC):c.9883C>T (p.Arg3295Cys) rs77303974
NM_201378.4(PLEC):c.9919G>A (p.Gly3307Arg) rs34132016
NM_201384.3(PLEC):c.58A>G (p.Ser20Gly) rs183111586

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