ClinVar Miner

List of variants in gene PLEC reported as uncertain significance by Athena Diagnostics Inc

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 65
Download table as spreadsheet
HGVS dbSNP
NM_000445.5(PLEC):c.10120G>A (p.Val3374Met) rs782748769
NM_000445.5(PLEC):c.10130T>C (p.Leu3377Pro) rs186417404
NM_000445.5(PLEC):c.11014C>T (p.Arg3672Cys)
NM_000445.5(PLEC):c.11101C>T (p.Arg3701Cys)
NM_000445.5(PLEC):c.1167C>G (p.His389Gln) rs1221901115
NM_000445.5(PLEC):c.11899G>A (p.Val3967Met) rs534537112
NM_000445.5(PLEC):c.118C>T (p.Arg40Trp) rs781877536
NM_000445.5(PLEC):c.12482C>T (p.Ser4161Phe) rs782074353
NM_000445.5(PLEC):c.128G>T (p.Gly43Val) rs781980239
NM_000445.5(PLEC):c.13531G>A (p.Gly4511Ser) rs782650176
NM_000445.5(PLEC):c.13550G>A (p.Arg4517His) rs782151802
NM_000445.5(PLEC):c.13717G>A (p.Val4573Met) rs573424409
NM_000445.5(PLEC):c.1535G>T (p.Arg512Leu) rs200328762
NM_000445.5(PLEC):c.158T>C (p.Leu53Pro) rs781861668
NM_000445.5(PLEC):c.194-3711_194-3639delinsAC rs1564189462
NM_000445.5(PLEC):c.194-5086G>A rs372851346
NM_000445.5(PLEC):c.194-655A>G rs191308779
NM_000445.5(PLEC):c.2050A>T (p.Ser684Cys) rs199843296
NM_000445.5(PLEC):c.2246C>T (p.Ala749Val) rs375178454
NM_000445.5(PLEC):c.2497C>T (p.Arg833Cys)
NM_000445.5(PLEC):c.2933G>C (p.Arg978Pro) rs782775290
NM_000445.5(PLEC):c.3289A>G (p.Thr1097Ala) rs185859960
NM_000445.5(PLEC):c.3437C>T (p.Pro1146Leu) rs782567448
NM_000445.5(PLEC):c.3523G>T (p.Ala1175Ser) rs370869846
NM_000445.5(PLEC):c.3676C>G (p.Gln1226Glu) rs1564083000
NM_000445.5(PLEC):c.3719G>A (p.Arg1240His) rs782011338
NM_000445.5(PLEC):c.3868G>A (p.Glu1290Lys) rs377125427
NM_000445.5(PLEC):c.38A>C (p.Glu13Ala) rs370431965
NM_000445.5(PLEC):c.4039C>T (p.Arg1347Cys) rs372256096
NM_000445.5(PLEC):c.4051A>C (p.Ser1351Arg) rs782377096
NM_000445.5(PLEC):c.4250C>T (p.Ala1417Val) rs781873089
NM_000445.5(PLEC):c.4427G>A (p.Arg1476His) rs561225406
NM_000445.5(PLEC):c.4444C>T (p.Arg1482Cys) rs782436596
NM_000445.5(PLEC):c.4607G>A (p.Arg1536His) rs782666455
NM_000445.5(PLEC):c.4798A>G (p.Ser1600Gly) rs1212000414
NM_000445.5(PLEC):c.5329C>T (p.Arg1777Trp) rs782410213
NM_000445.5(PLEC):c.5495G>A (p.Arg1832His) rs782438887
NM_000445.5(PLEC):c.5813G>A (p.Gly1938Glu) rs377030479
NM_000445.5(PLEC):c.5822A>G (p.Glu1941Gly)
NM_000445.5(PLEC):c.6019G>A (p.Glu2007Lys)
NM_000445.5(PLEC):c.6155G>A (p.Arg2052Gln) rs546512137
NM_000445.5(PLEC):c.6347C>T (p.Ala2116Val) rs782278608
NM_000445.5(PLEC):c.6496C>T (p.Arg2166Cys)
NM_000445.5(PLEC):c.6782G>A (p.Arg2261His) rs369374252
NM_000445.5(PLEC):c.6926G>A (p.Arg2309Gln) rs782316711
NM_000445.5(PLEC):c.7474G>A (p.Glu2492Lys)
NM_000445.5(PLEC):c.7733G>A (p.Ser2578Asn)
NM_000445.5(PLEC):c.7798C>A (p.Leu2600Met) rs1564000724
NM_000445.5(PLEC):c.7819C>T (p.Arg2607Trp)
NM_000445.5(PLEC):c.7834G>C (p.Glu2612Gln) rs200488179
NM_000445.5(PLEC):c.8132G>A (p.Arg2711Gln) rs200239963
NM_000445.5(PLEC):c.8396G>A (p.Arg2799His) rs201916690
NM_000445.5(PLEC):c.8587G>A (p.Asp2863Asn) rs200814155
NM_000445.5(PLEC):c.8901C>T (p.Asp2967=)
NM_000445.5(PLEC):c.9104G>A (p.Arg3035Gln) rs200176579
NM_000445.5(PLEC):c.9475C>T (p.Arg3159Cys) rs370266957
NM_000445.5(PLEC):c.9556G>A (p.Ala3186Thr) rs201030020
NM_000445.5(PLEC):c.9830C>T (p.Thr3277Met)
NM_000445.5(PLEC):c.9836C>T (p.Thr3279Met) rs781828296
NM_000445.5(PLEC):c.9896G>A (p.Arg3299His) rs571590501
NM_201380.4(PLEC):c.247C>T (p.Arg83Cys) rs200878086
NM_201380.4(PLEC):c.392C>T (p.Pro131Leu) rs560175252
NM_201380.4(PLEC):c.416T>C (p.Val139Ala) rs201910266
NM_201380.4(PLEC):c.481C>T (p.Arg161Trp)
NM_201382.4(PLEC):c.98C>T (p.Ala33Val) rs782610872

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.