List of variants in gene NEK8 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_178170.3(NEK8):c.419G>T (p.Arg140Leu)	rs141599330	0.00048
NM_178170.3(NEK8):c.817C>T (p.Arg273Cys)	rs371673804	0.00025
NM_178170.3(NEK8):c.583G>A (p.Glu195Lys)	rs752331372	0.00011
NM_178170.3(NEK8):c.1179C>G (p.Ile393Met)	rs775138270	0.00005
NM_178170.3(NEK8):c.1096G>A (p.Gly366Ser)	rs200428176	0.00001
NM_178170.3(NEK8):c.185A>G (p.Asn62Ser)	rs1367917533	0.00001
NM_178170.3(NEK8):c.57C>T (p.His19=)	rs748430513	0.00001
NM_178170.3(NEK8):c.133C>T (p.Arg45Trp)	rs1567759130
NM_178170.3(NEK8):c.145C>G (p.Gln49Glu)	rs2151731531
NM_178170.3(NEK8):c.2036T>C (p.Leu679Pro)
NM_178170.3(NEK8):c.34A>G (p.Arg12Gly)
NM_178170.3(NEK8):c.508A>T (p.Ile170Phe)	rs2544438828
NM_178170.3(NEK8):c.568G>A (p.Gly190Ser)

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