List of variants in gene PEX5 reported as benign by Invitae

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_001351132.2(PEX5):c.815T>C (p.Met272Thr)	rs76708142	0.02223
NM_001351132.2(PEX5):c.1718+13A>G	rs116873137	0.01093
NM_001351132.2(PEX5):c.998G>A (p.Arg333His)	rs59209175	0.00776
NM_001351132.2(PEX5):c.1632G>A (p.Ala544=)	rs115338343	0.00644
NM_001351132.2(PEX5):c.1053G>A (p.Leu351=)	rs61740909	0.00290
NM_001351132.2(PEX5):c.1521C>T (p.Ala507=)	rs150761638	0.00221
NM_001351132.2(PEX5):c.604G>C (p.Val202Leu)	rs149102738	0.00209
NM_001351132.2(PEX5):c.471C>T (p.Ala157=)	rs144331955	0.00108
NM_001351132.2(PEX5):c.658C>T (p.Arg220Trp)	rs200020561	0.00103
NM_001351132.2(PEX5):c.1653C>G (p.Leu551=)	rs200215904	0.00010
NM_001351132.2(PEX5):c.381T>C (p.Asp127=)	rs201467035	0.00001
NM_001351132.2(PEX5):c.1394+14dup	rs1186018434
NM_001351132.2(PEX5):c.1413G>C (p.Val471=)	rs115760878
NM_001351132.2(PEX5):c.148-15_148-12del	rs774517551
NM_001351132.2(PEX5):c.754-8del
NM_001351132.2(PEX5):c.966+24dup	rs1944415107

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