List of variants in gene NDUFS8 reported as uncertain significance by GeneDx

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_002496.4(NDUFS8):c.19C>A (p.Pro7Thr)	rs142658611	0.00081
NM_002496.4(NDUFS8):c.64C>T (p.Pro22Ser)	rs369602258	0.00012
NM_002496.4(NDUFS8):c.121A>C (p.Met41Leu)	rs149590243	0.00007
NM_002496.4(NDUFS8):c.229C>T (p.Arg77Trp)	rs146766138	0.00002
NM_002496.4(NDUFS8):c.313C>T (p.Pro105Ser)	rs863224114	0.00001
NM_002496.4(NDUFS8):c.592G>A (p.Glu198Lys)	rs1367957130	0.00001
NM_002496.4(NDUFS8):c.611A>T (p.Gln204Leu)	rs780162910	0.00001
NM_002496.4(NDUFS8):c.111G>C (p.Lys37Asn)
NM_002496.4(NDUFS8):c.197G>C (p.Arg66Pro)
NM_002496.4(NDUFS8):c.328C>T (p.Arg110Cys)	rs1002714490
NM_002496.4(NDUFS8):c.329G>T (p.Arg110Leu)
NM_002496.4(NDUFS8):c.347T>C (p.Leu116Pro)	rs2134414582
NM_002496.4(NDUFS8):c.424C>T (p.Arg142Cys)
NM_002496.4(NDUFS8):c.502-3C>T	rs2495588179

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