NUPR2[gene] and "single gene"[properties] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2348676	NM_001145712.2(NUPR2):c.17A>T (p.Glu6Val)	NUPR2 (E6V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348675	NM_001145712.2(NUPR2):c.16G>C (p.Glu6Gln)	NUPR2 (E6Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2657517	NM_001145712.2(NUPR2):c.15A>T (p.Ala5=)	NUPR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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