List of variants in gene COQ8A reported by Mayo Clinic Laboratories, Mayo Clinic

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_020247.5(COQ8A):c.1660-9T>C	rs7552783	0.45219
NM_020247.5(COQ8A):c.1716T>C (p.Ser572=)	rs3738725	0.42035
NM_020247.5(COQ8A):c.117G>A (p.Ala39=)	rs11549708	0.16388
NM_020247.5(COQ8A):c.255T>G (p.His85Gln)	rs2297411	0.04148
NM_020247.5(COQ8A):c.993C>T (p.Phe331=)	rs41303129	0.01390
NM_020247.5(COQ8A):c.63G>A (p.Ala21=)	rs11549709	0.01280
NM_020247.5(COQ8A):c.1053C>T (p.Gly351=)	rs55958233	0.01103
NM_020247.5(COQ8A):c.1185C>T (p.Ile395=)	rs17849927	0.00488
NM_020247.5(COQ8A):c.67G>A (p.Val23Met)	rs35582308	0.00058
NM_020247.5(COQ8A):c.1042C>T (p.Arg348Ter)	rs771578775	0.00006
NM_020247.5(COQ8A):c.358G>A (p.Val120Met)	rs376347405	0.00001
NM_020247.5(COQ8A):c.1440C>T (p.Phe480=)	rs12593
NM_020247.5(COQ8A):c.1671C>A (p.Asp557Glu)	rs370899166
NM_020247.5(COQ8A):c.1831A>G (p.Arg611Gly)	rs1553281394
NM_020247.5(COQ8A):c.1936C>A (p.Gln646Lys)	rs555171534
NM_020247.5(COQ8A):c.220G>A (p.Gly74Ser)	rs778948697

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