List of variants in gene PEX14 reported as likely benign for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_004565.3(PEX14):c.85-288A>G	rs12408852	0.02580
NM_004565.3(PEX14):c.169+68C>T	rs115344694	0.01583
NM_004565.3(PEX14):c.586-257C>T	rs147208801	0.01111
NM_004565.3(PEX14):c.768G>A (p.Val256=)	rs36083022	0.01070
NM_004565.3(PEX14):c.959G>A (p.Arg320Lys)	rs12070353	0.00912
NM_004565.3(PEX14):c.213C>G (p.Gly71=)	rs41274482	0.00899
NM_004565.3(PEX14):c.170-143C>T	rs145432748	0.00726
NM_004565.3(PEX14):c.385-176G>A	rs150713371	0.00628
NM_004565.3(PEX14):c.795A>G (p.Ser265=)	rs41274484	0.00451
NM_004565.3(PEX14):c.360A>G (p.Ala120=)	rs148479162	0.00021
NM_004565.3(PEX14):c.297C>T (p.Tyr99=)	rs371473184	0.00004
NM_004565.3(PEX14):c.81G>A (p.Pro27=)	rs1557810674
NM_004565.3(PEX14):c.939G>T (p.Val313=)	rs1408463885

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