"Ambry Genetics"[submitter] AND "SUV39H2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2488990	NM_001193424.2(SUV39H2):c.43C>A (p.Pro15Thr)	SUV39H2 (P15T)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2613711	NM_001193424.2(SUV39H2):c.489G>T (p.Glu163Asp)	SUV39H2 (E163D +1 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2246667	NM_001193424.2(SUV39H2):c.526A>C (p.Lys176Gln)	SUV39H2 (K116Q +1 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2332837	NM_001193424.2(SUV39H2):c.614A>C (p.Glu205Ala)	SUV39H2 (E145A +1 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2403926	NM_001193424.2(SUV39H2):c.781C>T (p.Arg261Cys)	DCLRE1C, SUV39H2 (R261C +1 more)	Single nucleotide variant (3 prime UTR variant +3 more)	Inborn genetic diseases	GLikely benign
Select item 2622610	NM_001193424.2(SUV39H2):c.899A>G (p.Lys300Arg)	DCLRE1C, SUV39H2 (K240R +3 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance

ClinVar