"Institute for Clinical Genetics, University Hospital TU Dresden, Univ - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2575987	NM_001042424.3(NSD2):c.1879G>T (p.Glu627Ter)	NSD2 (E627*)	Single nucleotide variant (nonsense)	not provided	GLikely pathogenic
Select item 2196053	NM_001042424.3(NSD2):c.2414T>C (p.Val805Ala)	NSD2 (V805A)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity