List of variants in gene COA8 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001370595.2(COA8):c.101G>T (p.Arg34Leu)	rs534048581	0.00030
NM_001370595.2(COA8):c.85G>A (p.Glu29Lys)	rs535382401	0.00014
NM_001370595.2(COA8):c.97G>A (p.Glu33Lys)	rs549170173	0.00010
NM_001370595.2(COA8):c.197G>A (p.Arg66Gln)	rs751876490	0.00008
NM_001370595.2(COA8):c.433G>A (p.Glu145Lys)	rs562472810	0.00002
NM_001370595.2(COA8):c.172C>A (p.Pro58Thr)	rs774599759	0.00001
NM_001370595.2(COA8):c.106G>T (p.Asp36Tyr)
NM_001370595.2(COA8):c.40C>T (p.Pro14Ser)	rs2274268

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