ClinVar Miner

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

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Gene type:
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Total variants: 24
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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
NM_000445.4(PLEC):c.10042G>A (p.Gly3348Arg) rs34132016
NM_000445.4(PLEC):c.10840C>T (p.Leu3614=) rs200006106
NM_000445.4(PLEC):c.11001C>T (p.Tyr3667=) rs28455570
NM_000445.4(PLEC):c.11170C>T (p.Leu3724=) rs17062686
NM_000445.4(PLEC):c.12865G>A (p.Val4289Ile) rs142946078
NM_000445.4(PLEC):c.1317G>A (p.Leu439=) rs190791617
NM_000445.4(PLEC):c.13329G>A (p.Thr4443=) rs115621402
NM_000445.4(PLEC):c.26G>A (p.Arg9Gln) rs138978753
NM_000445.4(PLEC):c.3838-9A>G rs57461687
NM_000445.4(PLEC):c.3950A>G (p.Lys1317Arg) rs200895043
NM_000445.4(PLEC):c.5558G>A (p.Arg1853Gln) rs147838690
NM_000445.4(PLEC):c.6150C>G (p.Arg2050=) rs376365984
NM_000445.4(PLEC):c.6489G>A (p.Glu2163=)
NM_000445.4(PLEC):c.7348G>A (p.Ala2450Thr) rs193257576
NM_000445.4(PLEC):c.7911G>A (p.Ala2637=) rs376112916
NM_000445.4(PLEC):c.8106C>T (p.Gly2702=) rs35139934
NM_000445.4(PLEC):c.8511C>G (p.Ile2837Met) rs62641758
NM_000445.4(PLEC):c.8901C>G (p.Asp2967Glu) rs58308209
NM_000445.4(PLEC):c.9432C>T (p.Phe3144=) rs200895343
NM_201384.2(PLEC):c.58A>G (p.Ser20Gly) rs183111586

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