List of variants in gene COG7 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_153603.4(COG7):c.2283C>T (p.Thr761=)	rs144814374	0.00150
NM_153603.4(COG7):c.1455C>T (p.Phe485=)	rs116153163	0.00068
NM_153603.4(COG7):c.2052G>A (p.Ser684=)	rs142744907	0.00060
NM_153603.4(COG7):c.2013G>A (p.Leu671=)	rs370447404	0.00012
NM_153603.4(COG7):c.525G>A (p.Val175=)	rs144180834	0.00011
NM_153603.4(COG7):c.1206G>A (p.Ala402=)	rs777152433	0.00008

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