"Illumina Laboratory Services, Illumina"[submitter] AND "LOC126807509" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 350837	NM_014402.5(UQCRQ):c.-31del	LOC126807509, UQCRQ	Deletion (5 prime UTR variant)	Mitochondrial complex III deficiency nuclear type 1	GUncertain significance
Select item 350838	NM_014402.5(UQCRQ):c.-18G>C	LOC126807509, UQCRQ	Single nucleotide variant (5 prime UTR variant)	Mitochondrial complex III deficiency nuclear type 4	GUncertain significance
Select item 904277	NM_014402.5(UQCRQ):c.-16C>T	LOC126807509, UQCRQ	Single nucleotide variant (5 prime UTR variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 350839	NM_014402.5(UQCRQ):c.45C>T (p.Ile15=)	UQCRQ, LOC126807509	Single nucleotide variant (synonymous variant)	Mitochondrial complex III deficiency nuclear type 4 +1 more	GConflicting classifications of pathogenicity
Select item 669826	NM_014402.5(UQCRQ):c.90C>T (p.Val30=)	LOC126807509, UQCRQ	Single nucleotide variant (synonymous variant)	Mitochondrial complex III deficiency nuclear type 4 +1 more	GConflicting classifications of pathogenicity
Select item 137891	NM_014402.5(UQCRQ):c.108C>G (p.Pro36=)	LOC126807509, UQCRQ	Single nucleotide variant (synonymous variant)	not specified +2 more	GConflicting classifications of pathogenicity

ClinVar