List of variants in gene COX10 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001303.4(COX10):c.1027T>C (p.Cys343Arg)	rs200818252	0.00041
NM_001303.4(COX10):c.311C>T (p.Pro104Leu)	rs202207627	0.00016
NM_001303.4(COX10):c.307T>G (p.Ser103Ala)	rs200480915	0.00008
NM_001303.4(COX10):c.625T>C (p.Phe209Leu)	rs767032314	0.00008
NM_001303.4(COX10):c.1192C>T (p.Arg398Cys)	rs368724576	0.00006
NM_001303.4(COX10):c.1061G>A (p.Arg354Gln)	rs745492359	0.00005
NM_001303.4(COX10):c.173G>A (p.Arg58His)	rs772223730	0.00005
NM_001303.4(COX10):c.1070C>T (p.Ala357Val)	rs148783821	0.00004
NM_001303.4(COX10):c.394G>T (p.Asp132Tyr)	rs141549844	0.00004
NM_001303.4(COX10):c.1169C>T (p.Ala390Val)	rs749603596	0.00002
NM_001303.4(COX10):c.1186G>A (p.Gly396Ser)	rs142336139	0.00001
NM_001303.4(COX10):c.-89G>C	rs188803165
NM_001303.4(COX10):c.-89G>T	rs188803165
NM_001303.4(COX10):c.1096G>A (p.Val366Met)	rs111541535
NM_001303.4(COX10):c.520G>A (p.Ala174Thr)	rs2142200228

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