"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "DNAH9"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3380465	NM_001372.4(DNAH9):c.5814G>A (p.Gln1938=)	DNAH9	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 1416282	NM_001372.4(DNAH9):c.6313C>T (p.Arg2105Trp)	DNAH9 (R2105W)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2227582	NM_001372.4(DNAH9):c.7297T>G (p.Ser2433Ala)	DNAH9 (S2433A)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2048419	NM_001372.4(DNAH9):c.10778T>A (p.Met3593Lys)	DNAH9, LOC101928350 (M3593K)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3380466	NM_001372.4(DNAH9):c.11977G>A (p.Glu3993Lys)	DNAH9 (E305K +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3380467	NM_001372.4(DNAH9):c.13277del (p.Pro4426fs)	DNAH9 (P4426fs +1 more)	Deletion (frameshift variant)	not provided	GUncertain significance

ClinVar