List of variants in gene AP5Z1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_014855.3(AP5Z1):c.*532G>A	rs527985598	0.00387
NM_014855.3(AP5Z1):c.1557A>G (p.Gln519=)	rs201687417	0.00341
NM_014855.3(AP5Z1):c.881G>A (p.Arg294Gln)	rs200957609	0.00278
NM_014855.3(AP5Z1):c.481G>A (p.Val161Met)	rs191971593	0.00201
NM_014855.3(AP5Z1):c.1062C>T (p.His354=)	rs192441133	0.00114
NM_014855.3(AP5Z1):c.1155G>A (p.Ser385=)	rs370926189	0.00112
NM_014855.3(AP5Z1):c.558C>T (p.Tyr186=)	rs371534878	0.00092
NM_014855.3(AP5Z1):c.999C>T (p.Asp333=)	rs201196622	0.00079
NM_014855.3(AP5Z1):c.1773C>T (p.Tyr591=)	rs372922535	0.00073
NM_014855.3(AP5Z1):c.1964C>T (p.Ser655Leu)	rs61750324	0.00065
NM_014855.3(AP5Z1):c.849C>T (p.Ala283=)	rs572271008	0.00060
NM_014855.3(AP5Z1):c.1043C>T (p.Ser348Phe)	rs547137141	0.00044
NM_014855.3(AP5Z1):c.2400G>A (p.Arg800=)	rs368571200	0.00030
NM_014855.3(AP5Z1):c.258C>T (p.Cys86=)	rs369050534	0.00019
NM_014855.3(AP5Z1):c.636C>T (p.Thr212=)	rs777143531	0.00010
NM_014855.3(AP5Z1):c.1110C>T (p.Leu370=)	rs756954352	0.00006
NM_014855.3(AP5Z1):c.1527C>T (p.Phe509=)	rs745794388	0.00006
NM_014855.3(AP5Z1):c.543C>T (p.Val181=)	rs1050248739	0.00004
NM_014855.3(AP5Z1):c.660A>G (p.Thr220=)	rs756140557	0.00004
NM_014855.3(AP5Z1):c.894C>T (p.Phe298=)	rs777233282	0.00004
NM_014855.3(AP5Z1):c.678C>G (p.Leu226=)	rs771296028	0.00002
NM_014855.3(AP5Z1):c.392C>T (p.Ala131Val)	rs372539355	0.00001
NM_014855.3(AP5Z1):c.1018C>T (p.Pro340Ser)	rs561646689
NM_014855.3(AP5Z1):c.1239C>T (p.Phe413=)
NM_014855.3(AP5Z1):c.1266C>T (p.Ser422=)
NM_014855.3(AP5Z1):c.420G>A (p.Leu140=)
NM_014855.3(AP5Z1):c.957C>T (p.Asp319=)

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