"Equipe Genetique des Anomalies du Developpement, Université de Bourgo - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2443354	NM_015021.3(ZNF292):c.323+1G>A	ZNF292	Single nucleotide variant (splice donor variant)	Intellectual developmental disorder, autosomal dominant 64	GUncertain significance
Select item 1172644	NM_015021.3(ZNF292):c.3319C>T (p.Arg1107Ter)	ZNF292 (R1107* +1 more)	Single nucleotide variant (nonsense)	Motor delay +1 more	GLikely pathogenic
Select item 2443353	NM_015021.3(ZNF292):c.4933C>T (p.Gln1645Ter)	ZNF292 (Q1505* +1 more)	Single nucleotide variant (nonsense)	Intellectual developmental disorder, autosomal dominant 64	GUncertain significance
Select item 981392	NM_015021.3(ZNF292):c.6160_6161del (p.Glu2054fs)	ZNF292 (E1914fs +1 more)	Deletion (frameshift variant)	Inborn genetic diseases +4 more	GPathogenic/Likely pathogenic
Select item 982198	NM_015021.3(ZNF292):c.6279dup (p.Arg2094fs)	ZNF292 (R1954fs +1 more)	Duplication (frameshift variant)	Intellectual developmental disorder, autosomal dominant 64	GPathogenic
Select item 2443355	NM_015021.3(ZNF292):c.7460del (p.Leu2487fs)	ZNF292 (L2347fs +1 more)	Deletion (frameshift variant)	Intellectual developmental disorder, autosomal dominant 64	GUncertain significance
Select item 2443356	NM_015021.3(ZNF292):c.7614del (p.Asn2538fs)	ZNF292 (N2398fs +1 more)	Deletion (frameshift variant)	Intellectual developmental disorder, autosomal dominant 64	GLikely benign

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