List of variants in gene PEX6 reported as uncertain significance by Illumina Laboratory Services, Illumina

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 48

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HGVS	dbSNP	gnomAD frequency
NM_000287.4(PEX6):c.1718C>T (p.Thr573Ile)	rs140769712	0.00122
NM_000287.4(PEX6):c.853C>G (p.Pro285Ala)	rs61753220	0.00067
NM_000287.4(PEX6):c.1234-11A>G	rs201879957	0.00041
NM_000287.4(PEX6):c.*343G>C	rs117055658	0.00037
NM_000287.4(PEX6):c.503C>T (p.Pro168Leu)	rs200026148	0.00037
NM_000287.4(PEX6):c.1670A>G (p.Asn557Ser)	rs138621982	0.00030
NM_000287.4(PEX6):c.25C>T (p.Leu9=)	rs183449855	0.00029
NM_000287.4(PEX6):c.2700C>T (p.Asn900=)	rs533766104	0.00029
NM_000287.3(PEX6):c.-79C>T	rs186587060	0.00024
NM_000287.4(PEX6):c.2183C>T (p.Pro728Leu)	rs142899308	0.00016
NM_000287.4(PEX6):c.1606C>T (p.Arg536Trp)	rs368752843	0.00012
NM_000287.4(PEX6):c.1387A>G (p.Thr463Ala)	rs182308788	0.00005
NM_000287.4(PEX6):c.1877G>A (p.Arg626Gln)	rs79351868	0.00005
NM_000287.3(PEX6):c.-39G>A	rs76974379	0.00004
NM_000287.4(PEX6):c.2642G>A (p.Arg881His)	rs751377690	0.00004
NM_000287.4(PEX6):c.2736G>A (p.Ala912=)	rs202049230	0.00004
NM_000287.4(PEX6):c.690G>A (p.Glu230=)	rs368341252	0.00004
NM_000287.4(PEX6):c.870G>C (p.Glu290Asp)	rs150358700	0.00004
NM_000287.4(PEX6):c.939T>C (p.Pro313=)	rs151234121	0.00004
NM_000287.3(PEX6):c.-62C>A	rs886061413	0.00003
NM_000287.4(PEX6):c.*168C>T	rs886061410	0.00003
NM_000287.4(PEX6):c.1234-10C>T	rs370661410	0.00003
NM_000287.4(PEX6):c.295C>T (p.Arg99Trp)	rs772383329	0.00003
NM_000287.3(PEX6):c.-71C>G	rs886061414	0.00001
NM_000287.4(PEX6):c.1085T>C (p.Ile362Thr)	rs571650965	0.00001
NM_000287.4(PEX6):c.1130+2T>C	rs1416001981	0.00001
NM_000287.4(PEX6):c.1365A>G (p.Pro455=)	rs759402659	0.00001
NM_000287.4(PEX6):c.1367+10G>A	rs776610051	0.00001
NM_000287.4(PEX6):c.1931G>A (p.Arg644Gln)	rs746117128	0.00001
NM_000287.4(PEX6):c.2547C>T (p.Asn849=)	rs1171568759	0.00001
NM_000287.4(PEX6):c.2877A>G (p.Gln959=)	rs562040179	0.00001
NM_000287.4(PEX6):c.*368G>A	rs866465109
NM_000287.4(PEX6):c.*407T>G	rs886061409
NM_000287.4(PEX6):c.106C>A (p.Leu36Met)	rs758416830
NM_000287.4(PEX6):c.1092A>G (p.Gln364=)	rs1241222298
NM_000287.4(PEX6):c.1110A>G (p.Gly370=)	rs886061411
NM_000287.4(PEX6):c.1415C>T (p.Pro472Leu)	rs1769951744
NM_000287.4(PEX6):c.235G>A (p.Ala79Thr)	rs61752141
NM_000287.4(PEX6):c.2471+5G>T	rs1213308057
NM_000287.4(PEX6):c.2601G>T (p.Leu867=)	rs1769712635
NM_000287.4(PEX6):c.2697A>G (p.Val899=)	rs892510772
NM_000287.4(PEX6):c.2907G>C (p.Arg969=)	rs145243129
NM_000287.4(PEX6):c.302C>G (p.Pro101Arg)	rs774813175
NM_000287.4(PEX6):c.410G>C (p.Arg137Pro)	rs1254025750
NM_000287.4(PEX6):c.49C>A (p.Pro17Thr)	rs918969564
NM_000287.4(PEX6):c.681G>A (p.Gln227=)	rs1770406319
NM_000287.4(PEX6):c.718G>A (p.Ala240Thr)	rs886061412
NM_000287.4(PEX6):c.76G>C (p.Gly26Arg)	rs1268867658

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