ClinVar Miner

List of variants in gene PEX6 reported as likely benign by PreventionGenetics, part of Exact Sciences

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Total variants: 51
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HGVS dbSNP gnomAD frequency
NM_000287.4(PEX6):c.1646C>T (p.Ala549Val) rs115960224 0.00687
NM_000287.4(PEX6):c.813G>T (p.Ala271=) rs35503676 0.00583
NM_000287.4(PEX6):c.882+15_882+16del rs555409430 0.00189
NM_000287.4(PEX6):c.685A>G (p.Arg229Gly) rs146571927 0.00176
NM_000287.4(PEX6):c.1171G>A (p.Glu391Lys) rs150046979 0.00175
NM_000287.4(PEX6):c.1718C>T (p.Thr573Ile) rs140769712 0.00122
NM_000287.4(PEX6):c.1677C>A (p.Asp559Glu) rs61732159 0.00093
NM_000287.4(PEX6):c.-2C>G rs376675730 0.00036
NM_000287.4(PEX6):c.2700C>T (p.Asn900=) rs533766104 0.00029
NM_000287.4(PEX6):c.1884+3G>A rs377041406 0.00026
NM_000287.4(PEX6):c.306G>T (p.Ala102=) rs727504083 0.00026
NM_000287.4(PEX6):c.372G>C (p.Leu124=) rs752732049 0.00021
NM_000287.4(PEX6):c.2867C>T (p.Ala956Val) rs200115671 0.00014
NM_000287.4(PEX6):c.1773C>T (p.Leu591=) rs56328719 0.00009
NM_000287.4(PEX6):c.390C>T (p.Thr130=) rs753963225 0.00008
NM_000287.4(PEX6):c.1680C>T (p.Pro560=) rs372998833 0.00007
NM_000287.4(PEX6):c.2229T>C (p.His743=) rs145849057 0.00005
NM_000287.4(PEX6):c.2730G>A (p.Thr910=) rs774721609 0.00005
NM_000287.4(PEX6):c.411G>A (p.Arg137=) rs769196737 0.00004
NM_000287.4(PEX6):c.690G>A (p.Glu230=) rs368341252 0.00004
NM_000287.4(PEX6):c.939T>C (p.Pro313=) rs151234121 0.00004
NM_000287.4(PEX6):c.1207G>A (p.Asp403Asn) rs535326039 0.00003
NM_000287.4(PEX6):c.1137G>T (p.Arg379=) rs766574538 0.00002
NM_000287.4(PEX6):c.1746T>C (p.Asp582=) rs756462650 0.00002
NM_000287.4(PEX6):c.192C>G (p.Thr64=) rs1310661091 0.00002
NM_000287.4(PEX6):c.2643C>T (p.Arg881=) rs150853105 0.00002
NM_000287.4(PEX6):c.1260A>G (p.Pro420=) rs139409107 0.00001
NM_000287.4(PEX6):c.1392C>T (p.Ser464=) rs1345870957 0.00001
NM_000287.4(PEX6):c.1737G>A (p.Leu579=) rs766766609 0.00001
NM_000287.4(PEX6):c.1884A>G (p.Ala628=) rs779124738 0.00001
NM_000287.4(PEX6):c.804C>T (p.Asp268=) rs761372470 0.00001
NM_000287.4(PEX6):c.84G>A (p.Pro28=) rs1236425028 0.00001
NM_000287.4(PEX6):c.883-8T>C rs777174653 0.00001
NM_000287.4(PEX6):c.990C>T (p.His330=) rs947712788 0.00001
NM_000287.4(PEX6):c.-9C>T
NM_000287.4(PEX6):c.135G>A (p.Glu45=) rs2150240712
NM_000287.4(PEX6):c.1404A>G (p.Leu468=)
NM_000287.4(PEX6):c.1524G>A (p.Glu508=)
NM_000287.4(PEX6):c.1740T>G (p.Pro580=) rs2114242721
NM_000287.4(PEX6):c.1774G>A (p.Glu592Lys) rs375288192
NM_000287.4(PEX6):c.1887C>T (p.Gly629=)
NM_000287.4(PEX6):c.2095-21C>G
NM_000287.4(PEX6):c.2268A>T (p.Ala756=) rs1769801311
NM_000287.4(PEX6):c.2300+26G>A
NM_000287.4(PEX6):c.2301-5_2301-2del rs748032659
NM_000287.4(PEX6):c.235G>A (p.Ala79Thr) rs61752141
NM_000287.4(PEX6):c.2865C>T (p.Ala955=) rs1407928755
NM_000287.4(PEX6):c.445C>T (p.Leu149=) rs2150240046
NM_000287.4(PEX6):c.819C>T (p.Val273=) rs748814053
NM_000287.4(PEX6):c.882+9A>G
NM_000287.4(PEX6):c.924C>T (p.Ser308=)

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