ClinVar for MedGen (Select 1794188) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1526397	NM_001372106.1(DNAH10):c.12241C>T (p.Arg4081Cys)	DNAH10, DNAH10OS (R3963C +1 more)	Single nucleotide variant (missense variant)	Spermatogenic failure 56	GUncertain significance
Select item 1526396	NM_001372106.1(DNAH10):c.7955C>T (p.Thr2652Met)	DNAH10 (T2534M +1 more)	Single nucleotide variant (missense variant)	Spermatogenic failure 56	GUncertain significance
Select item 1526395	NM_001372106.1(DNAH10):c.6017G>A (p.Arg2006Gln)	DNAH10 (R1888Q +1 more)	Single nucleotide variant (missense variant)	Spermatogenic failure 56	GUncertain significance
Select item 1217310	NM_001372106.1(DNAH10):c.13192G>A (p.Gly4398Arg)	DNAH10, DNAH10OS (G4280R +1 more)	Single nucleotide variant (missense variant)	Spermatogenic failure 56	GLikely pathogenic
Select item 1217309	NM_001372106.1(DNAH10):c.7614dup (p.Glu2539fs)	DNAH10 (E2421fs +1 more)	Duplication (frameshift variant)	Spermatogenic failure 56	GPathogenic
Select item 1217308	NM_001372106.1(DNAH10):c.12589del (p.Ser4197fs)	DNAH10, DNAH10OS (S4079fs +1 more)	Deletion (frameshift variant)	Spermatogenic failure 56	GPathogenic

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