List of variants in gene COG4 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_015386.3(COG4):c.1017G>A (p.Gln339=)	rs138874791	0.00177
NM_015386.3(COG4):c.592C>T (p.Arg198Cys)	rs118183032	0.00133
NM_015386.3(COG4):c.539A>G (p.Lys180Arg)	rs138693104	0.00036
NM_015386.3(COG4):c.558T>C (p.Asp186=)	rs376885733	0.00018
NM_015386.3(COG4):c.1005C>T (p.Phe335=)	rs183569708	0.00012
NM_015386.3(COG4):c.2247C>A (p.Ile749=)	rs767522005	0.00011

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