"Mendelics"[submitter] AND "WNT10A"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 334394	NM_025216.3(WNT10A):c.208C>T (p.Arg70Trp)	WNT10A (R70W)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 4 +4 more	GConflicting classifications of pathogenicity
Select item 4461	NM_025216.3(WNT10A):c.321C>A (p.Cys107Ter)	WNT10A (C107*)	Single nucleotide variant (nonsense)	Odonto-onycho-dermal dysplasia +7 more	GPathogenic
Select item 225515	NM_025216.3(WNT10A):c.511C>T (p.Arg171Cys)	WNT10A (R171C)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 2 +4 more	GConflicting classifications of pathogenicity
Select item 30567	NM_025216.3(WNT10A):c.649G>A (p.Asp217Asn)	WNT10A (D217N)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 4 +3 more	GConflicting classifications of pathogenicity
Select item 4462	NM_025216.3(WNT10A):c.682T>A (p.Phe228Ile)	WNT10A (F228I)	Single nucleotide variant (missense variant)	Ectodermal dysplasia +8 more	GConflicting classifications of pathogenicity
Select item 334414	NM_025216.3(WNT10A):c.1087A>C (p.Asn363His)	WNT10A (N363H)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 4 +4 more	GConflicting classifications of pathogenicity

ClinVar