Related gene-specific medical variations for Gene (Select 101927765) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3058720	NM_001206641.3(COA6):c.45G>A (p.Val15=)	COA6, COA6-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	COA6-related condition	GLikely benign
Select item 3024924	NM_001206641.3(COA6):c.39C>A (p.Arg13=)	COA6, COA6-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2582873	NM_001206641.3(COA6):c.47G>T (p.Ser16Ile)	COA6, COA6-AS1 (S16I)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 514919	NM_001206641.3(COA6):c.72T>C (p.Ser24=)	COA6, COA6-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 510592	NM_001206641.3(COA6):c.-11A>G	COA6, COA6-AS1	Single nucleotide variant (non-coding transcript variant +2 more)	not provided	GLikely benign
Select item 510543	NM_001206641.3(COA6):c.90G>A (p.Glu30=)	COA6, COA6-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not specified +1 more	GLikely benign
Select item 380009	NM_001206641.3(COA6):c.47G>C (p.Ser16Thr)	COA6, COA6-AS1 (S16T)	Single nucleotide variant (non-coding transcript variant +1 more)	Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4 +1 more	GBenign

ClinVar