ClinVar Miner

List of variants in gene PEX6 reported as likely benign

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Total variants: 24
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HGVS dbSNP
NM_000287.4(PEX6):c.*319C>T rs736158
NM_000287.4(PEX6):c.1171G>A (p.Glu391Lys) rs150046979
NM_000287.4(PEX6):c.1234-8_1234-7dup rs200121485
NM_000287.4(PEX6):c.1491C>T (p.Ser497=) rs79238506
NM_000287.4(PEX6):c.1646C>T (p.Ala549Val) rs115960224
NM_000287.4(PEX6):c.1677C>A (p.Asp559Glu) rs61732159
NM_000287.4(PEX6):c.1802G>A (p.Arg601Gln) rs34324426
NM_000287.4(PEX6):c.207C>T (p.Pro69=) rs11539736
NM_000287.4(PEX6):c.210G>A (p.Gly70=) rs398123304
NM_000287.4(PEX6):c.235G>C (p.Ala79Pro) rs61752141
NM_000287.4(PEX6):c.2364G>A (p.Val788=) rs2274515
NM_000287.4(PEX6):c.2426C>T (p.Ala809Val) rs35830695
NM_000287.4(PEX6):c.2436G>A (p.Arg812=) rs61732156
NM_000287.4(PEX6):c.2730G>A (p.Thr910=) rs774721609
NM_000287.4(PEX6):c.2770G>T (p.Ala924Ser) rs34551839
NM_000287.4(PEX6):c.2867C>T (p.Ala956Val) rs200115671
NM_000287.4(PEX6):c.2936C>T (p.Ala979Val) rs115180949
NM_000287.4(PEX6):c.330C>G (p.Thr110=) rs140486558
NM_000287.4(PEX6):c.685A>G (p.Arg229Gly) rs146571927
NM_000287.4(PEX6):c.804C>T (p.Asp268=) rs761372470
NM_000287.4(PEX6):c.813G>T (p.Ala271=) rs35503676
NM_000287.4(PEX6):c.853C>G (p.Pro285Ala) rs61753220
NM_000287.4(PEX6):c.882+15_882+16del rs555409430
NM_000287.4(PEX6):c.969C>T (p.Ile323=)

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