"Revvity Omics, Revvity"[submitter] AND "ZMYND11"[gene] - ClinVar - NCBI

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2438665	NM_001370100.5(ZMYND11):c.64A>G (p.Ile22Val)	ZMYND11 (I22V)	Single nucleotide variant (missense variant +3 more)	Intellectual disability, autosomal dominant 30 +1 more	GUncertain significance
Select item 2438662	NM_001370100.5(ZMYND11):c.142C>T (p.His48Tyr)	ZMYND11 (H26Y +3 more)	Single nucleotide variant (missense variant +2 more)	Intellectual disability, autosomal dominant 30	GUncertain significance
Select item 2438664	NM_001370100.5(ZMYND11):c.812A>G (p.Asn271Ser)	ZMYND11 (N114S +13 more)	Single nucleotide variant (missense variant +2 more)	Intellectual disability, autosomal dominant 30	GUncertain significance
Select item 2690462	NM_001370100.5(ZMYND11):c.906A>C (p.Glu302Asp)	ZMYND11 (E145D +14 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2438663	NM_001370100.5(ZMYND11):c.1000C>T (p.Arg334Trp)	ZMYND11 (R177W +14 more)	Single nucleotide variant (missense variant +1 more)	Intellectual disability, autosomal dominant 30	GUncertain significance
Select item 2438661	NM_001370100.5(ZMYND11):c.1199G>A (p.Arg400His)	ZMYND11 (R243H +13 more)	Single nucleotide variant (missense variant +2 more)	Intellectual disability, autosomal dominant 30	GUncertain significance
Select item 1311426	NM_001370100.5(ZMYND11):c.1273C>T (p.Pro425Ser)	LOC126860802, ZMYND11 (P268S +15 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2438659	NM_001370100.5(ZMYND11):c.1370C>T (p.Thr457Ile)	LOC126860802, ZMYND11 (T300I +15 more)	Single nucleotide variant (missense variant +1 more)	Intellectual disability, autosomal dominant 30	GUncertain significance