ClinVar Miner

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

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Total variants: 25
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HGVS dbSNP
NM_000445.4(PLEC):c.10042G>A (p.Gly3348Arg) rs34132016
NM_000445.4(PLEC):c.10449T>A (p.Val3483=)
NM_000445.4(PLEC):c.12752C>G (p.Ala4251Gly) rs368212208
NM_000445.4(PLEC):c.12898C>T (p.Pro4300Ser) rs202040785
NM_000445.4(PLEC):c.2349C>T (p.Thr783=) rs371267446
NM_000445.4(PLEC):c.2539-8C>T rs201818691
NM_000445.4(PLEC):c.2632G>A (p.Val878Met) rs200647397
NM_000445.4(PLEC):c.2907C>T (p.Asp969=)
NM_000445.4(PLEC):c.2910G>A (p.Ala970=)
NM_000445.4(PLEC):c.3582C>T (p.His1194=)
NM_000445.4(PLEC):c.4311C>T (p.Asp1437=) rs111282136
NM_000445.4(PLEC):c.4527G>A (p.Ala1509=) rs782202249
NM_000445.4(PLEC):c.4679G>A (p.Arg1560Gln) rs201430180
NM_000445.4(PLEC):c.4732C>T (p.Arg1578Cys) rs2857824
NM_000445.4(PLEC):c.5110G>A (p.Gly1704Ser) rs373952777
NM_000445.4(PLEC):c.5385G>A (p.Leu1795=) rs186670912
NM_000445.4(PLEC):c.5541C>T (p.Ala1847=) rs782259899
NM_000445.4(PLEC):c.5552C>T (p.Ala1851Val) rs542642242
NM_000445.4(PLEC):c.5557C>T (p.Arg1853Trp) rs200575795
NM_000445.4(PLEC):c.5793C>T (p.Ser1931=) rs115735672
NM_000445.4(PLEC):c.621C>T (p.Cys207=) rs189256993
NM_000445.4(PLEC):c.6505G>A (p.Ala2169Thr) rs370942881
NM_000445.4(PLEC):c.6867G>A (p.Thr2289=) rs373922545
NM_000445.4(PLEC):c.8093G>A (p.Arg2698Gln) rs28526657
NM_201384.2(PLEC):c.33C>T (p.Pro11=)

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