Related gene-specific medical variations for Gene (Select 79723) - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3323702	NM_001193424.2(SUV39H2):c.1139T>C (p.Ile380Thr)	DCLRE1C, SUV39H2 (I200T +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3323701	NM_001193424.2(SUV39H2):c.719C>G (p.Pro240Arg)	DCLRE1C, SUV39H2 (P180R +1 more)	Single nucleotide variant (3 prime UTR variant +3 more)	not specified	GUncertain significance
Select item 3172315	NM_001193424.2(SUV39H2):c.1159C>G (p.His387Asp)	DCLRE1C, SUV39H2 (H387D +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3043912	NM_001193424.2(SUV39H2):c.850-295C>G	DCLRE1C, SUV39H2	Single nucleotide variant (3 prime UTR variant +2 more)	SUV39H2-related disorder	GLikely benign
Select item 3042857	NM_001350965.2(DCLRE1C):c.1812C>T (p.Cys604=)	DCLRE1C, SUV39H2	Single nucleotide variant (synonymous variant +2 more)	DCLRE1C-related disorder	GLikely benign
Select item 2688318	NM_001193424.2(SUV39H2):c.850-483T>G	DCLRE1C, SUV39H2	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GBenign
Select item 2622610	NM_001193424.2(SUV39H2):c.899A>G (p.Lys300Arg)	DCLRE1C, SUV39H2 (K240R +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2570766	NM_001350965.2(DCLRE1C):c.*44C>G	DCLRE1C, SUV39H2	Single nucleotide variant (3 prime UTR variant +2 more)	not provided	GLikely benign
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)	not specified	GLikely benign
Select item 1694558	NM_001193424.2(SUV39H2):c.850-352G>A	SUV39H2, DCLRE1C	Single nucleotide variant (3 prime UTR variant +2 more)	not provided	GLikely benign
Select item 1255460	NM_001193424.2(SUV39H2):c.850-305C>T	DCLRE1C, SUV39H2	Single nucleotide variant (3 prime UTR variant +2 more)	not provided +3 more	GBenign
Select item 711031	NM_001193424.2(SUV39H2):c.850-6G>C	DCLRE1C, SUV39H2	Single nucleotide variant (intron variant)	not provided	GBenign