"Genome-Nilou Lab"[submitter] AND "NME8"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 164798	NM_016616.5(NME8):c.128G>A (p.Arg43Lys)	NME8 (R43K)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign
Select item 164799	NM_016616.5(NME8):c.177C>T (p.Asp59=)	NME8	Single nucleotide variant (synonymous variant)	Primary ciliary dyskinesia +3 more	GBenign
Select item 164801	NM_016616.5(NME8):c.622T>C (p.Cys208Arg)	NME8 (C208R)	Single nucleotide variant (missense variant)	Primary ciliary dyskinesia +3 more	GBenign
Select item 164804	NM_016616.5(NME8):c.1140-10T>G	NME8	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 260754	NM_016616.5(NME8):c.1247+25A>G	NME8	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 260756	NM_016616.5(NME8):c.1544+22G>A	NME8	Single nucleotide variant (intron variant)	Primary ciliary dyskinesia 6 +2 more	GBenign

ClinVar