List of variants in gene PEX14 reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 29

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HGVS	dbSNP	gnomAD frequency
NM_004565.3(PEX14):c.213C>G (p.Gly71=)	rs41274482	0.00899
NM_004565.3(PEX14):c.36+8G>A	rs200154696	0.00107
NM_004565.3(PEX14):c.267C>G (p.Val89=)	rs146359055	0.00097
NM_004565.3(PEX14):c.602A>G (p.Asn201Ser)	rs142285791	0.00083
NM_004565.3(PEX14):c.29C>G (p.Pro10Arg)	rs12068754	0.00080
NM_004565.3(PEX14):c.78G>A (p.Glu26=)	rs144664869	0.00047
NM_004565.3(PEX14):c.1098G>T (p.Arg366=)	rs139610784	0.00029
NM_004565.3(PEX14):c.169+7G>C	rs376989411	0.00018
NM_004565.3(PEX14):c.303C>T (p.Pro101=)	rs199552789	0.00014
NM_004565.3(PEX14):c.1101C>T (p.Pro367=)	rs146053705	0.00013
NM_004565.3(PEX14):c.766G>A (p.Val256Met)	rs143378690	0.00009
NM_004565.3(PEX14):c.1013A>G (p.Asp338Gly)	rs201120958	0.00007
NM_004565.3(PEX14):c.26A>T (p.Gln9Leu)	rs201979629	0.00006
NM_004565.3(PEX14):c.819G>A (p.Ser273=)	rs139518305	0.00005
NM_004565.3(PEX14):c.330C>T (p.Gly110=)	rs772527603	0.00004
NM_004565.3(PEX14):c.*7G>T	rs367982022	0.00003
NM_004565.3(PEX14):c.807C>T (p.Asn269=)	rs757658916	0.00003
NM_004565.3(PEX14):c.-7C>T	rs774075581	0.00002
NM_004565.3(PEX14):c.170-4C>A	rs764907398	0.00002
NM_004565.3(PEX14):c.786C>T (p.Ser262=)	rs1286463670	0.00002
NM_004565.3(PEX14):c.849C>T (p.Pro283=)	rs752909373	0.00002
NM_004565.3(PEX14):c.-10C>T
NM_004565.3(PEX14):c.-9C>T
NM_004565.3(PEX14):c.169+5A>G
NM_004565.3(PEX14):c.299-8G>A	rs112851814
NM_004565.3(PEX14):c.447G>A (p.Glu149=)
NM_004565.3(PEX14):c.450C>G (p.Ala150=)
NM_004565.3(PEX14):c.678-4C>G
NM_004565.3(PEX14):c.987G>A (p.Glu329=)

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