"Revvity Omics, Revvity"[submitter] AND "DNAH8"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 572041	NM_001206927.2(DNAH8):c.2100T>G (p.Ile700Met)	DNAH8 (I700M +1 more)	Single nucleotide variant (missense variant)	Primary ciliary dyskinesia +1 more	GUncertain significance
Select item 454566	NM_001206927.2(DNAH8):c.3129T>A (p.Asp1043Glu)	DNAH8 (D1043E +1 more)	Single nucleotide variant (missense variant)	Spermatogenic failure 46 +3 more	GConflicting classifications of pathogenicity
Select item 2440919	NM_001206927.2(DNAH8):c.5768A>T (p.His1923Leu)	DNAH8 (H1706L +1 more)	Single nucleotide variant (missense variant)	Spermatogenic failure 46	GUncertain significance
Select item 407274	NM_001206927.2(DNAH8):c.8869C>T (p.Arg2957Cys)	DNAH8 (R2957C +1 more)	Single nucleotide variant (missense variant)	Spermatogenic failure 46 +1 more	GUncertain significance
Select item 2440921	NM_001206927.2(DNAH8):c.13082C>T (p.Pro4361Leu)	DNAH8 (P4144L +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2440920	NM_001206927.2(DNAH8):c.13546A>G (p.Asn4516Asp)	DNAH8 (N4299D +1 more)	Single nucleotide variant (missense variant)	Spermatogenic failure 46	GUncertain significance
Select item 414429	NM_001206927.2(DNAH8):c.13823C>T (p.Thr4608Met)	DNAH8 (T4608M +1 more)	Single nucleotide variant (missense variant)	Spermatogenic failure 46 +1 more	GConflicting classifications of pathogenicity

ClinVar