Related gene-specific medical variations for Gene (Select 126862326) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3203314	NM_012385.3(NUPR1):c.244C>T (p.Arg82Cys)	LOC126862326, NUPR1 (R100C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457258	NM_012385.3(NUPR1):c.220G>A (p.Glu74Lys)	LOC126862326, NUPR1 (E74K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362948	NM_012385.3(NUPR1):c.187G>A (p.Glu63Lys)	LOC126862326, NUPR1 (E63K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335868	NM_012385.3(NUPR1):c.236G>A (p.Gly79Glu)	LOC126862326, NUPR1 (G97E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318848	NM_012385.3(NUPR1):c.133C>T (p.Arg45Cys)	LOC126862326, NUPR1 (R45C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262944	NM_012385.3(NUPR1):c.225G>C (p.Arg75Ser)	LOC126862326, NUPR1 (R75S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar