List of variants in gene COX15 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_078470.6(COX15):c.1026C>T (p.Phe342=)	rs147724430	0.00264
NM_078470.6(COX15):c.135C>T (p.Thr45=)	rs373219878	0.00004
NM_078470.6(COX15):c.220C>T (p.Leu74=)
NM_078470.6(COX15):c.366A>G (p.Gln122=)

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