ClinVar Miner

List of variants in gene PEX6 reported as likely benign for Peroxisome biogenesis disorders, Zellweger syndrome spectrum

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Total variants: 35
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HGVS dbSNP
NM_000287.4(PEX6):c.1014C>T (p.Asp338=) rs140806942
NM_000287.4(PEX6):c.1047-4G>T rs748779475
NM_000287.4(PEX6):c.1171G>A (p.Glu391Lys) rs150046979
NM_000287.4(PEX6):c.1225T>C (p.Leu409=) rs1243719850
NM_000287.4(PEX6):c.1335C>G (p.Leu445=) rs142958800
NM_000287.4(PEX6):c.141G>C (p.Pro47=) rs1464923917
NM_000287.4(PEX6):c.1479+7G>A rs528161793
NM_000287.4(PEX6):c.1512T>C (p.Ser504=) rs1013102900
NM_000287.4(PEX6):c.1677C>A (p.Asp559Glu) rs61732159
NM_000287.4(PEX6):c.1718C>T (p.Thr573Ile) rs140769712
NM_000287.4(PEX6):c.1774G>A (p.Glu592Lys) rs375288192
NM_000287.4(PEX6):c.1821C>T (p.Ala607=) rs201730259
NM_000287.4(PEX6):c.2010C>T (p.Ala670=) rs759328524
NM_000287.4(PEX6):c.219G>A (p.Gln73=) rs191944205
NM_000287.4(PEX6):c.2229T>C (p.His743=) rs145849057
NM_000287.4(PEX6):c.235G>A (p.Ala79Thr) rs61752141
NM_000287.4(PEX6):c.2643C>T (p.Arg881=) rs150853105
NM_000287.4(PEX6):c.2700C>T (p.Asn900=) rs533766104
NM_000287.4(PEX6):c.2736G>A (p.Ala912=) rs202049230
NM_000287.4(PEX6):c.2867C>T (p.Ala956Val) rs200115671
NM_000287.4(PEX6):c.2907G>C (p.Arg969=) rs145243129
NM_000287.4(PEX6):c.2928G>A (p.Lys976=) rs1230978438
NM_000287.4(PEX6):c.306G>T (p.Ala102=) rs727504083
NM_000287.4(PEX6):c.372G>C (p.Leu124=) rs752732049
NM_000287.4(PEX6):c.39G>A (p.Pro13=) rs908372737
NM_000287.4(PEX6):c.402C>T (p.Pro134=) rs773371109
NM_000287.4(PEX6):c.411G>A (p.Arg137=) rs769196737
NM_000287.4(PEX6):c.657G>A (p.Gln219=) rs375588028
NM_000287.4(PEX6):c.669G>C (p.Val223=) rs899965642
NM_000287.4(PEX6):c.685A>G (p.Arg229Gly) rs146571927
NM_000287.4(PEX6):c.753C>A (p.Leu251=) rs898341197
NM_000287.4(PEX6):c.819C>T (p.Val273=) rs748814053
NM_000287.4(PEX6):c.882+8A>G rs368663953
NM_000287.4(PEX6):c.883-8T>C rs777174653
NM_000287.4(PEX6):c.970G>A (p.Glu324Lys) rs201678533

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