ClinVar (all) for Orgtrack (Select 509139) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2570648	NM_021005.4(NR2F2):c.23G>A (p.Trp8Ter)	NR2F2 (W8*)	Single nucleotide variant (nonsense +1 more)	NR2F2 associated disorders	GLikely pathogenic
Select item 2570647	NM_021005.4(NR2F2):c.1133_1134dup (p.Glu379Ter)	NR2F2 (E226* +2 more)	Duplication (nonsense)	NR2F2 associated disorders	GLikely pathogenic
Select item 2570646	NM_021005.4(NR2F2):c.275G>T (p.Gly92Val)	NR2F2 (G92V)	Single nucleotide variant (missense variant +1 more)	NR2F2 associated disorders	GUncertain significance
Select item 2570645	NM_021005.4(NR2F2):c.382C>T (p.Arg128Cys)	NR2F2 (R128C)	Single nucleotide variant (missense variant +1 more)	NR2F2 associated disorders	GUncertain significance
Select item 2570644	NM_021005.4(NR2F2):c.313C>A (p.Arg105Ser)	NR2F2 (R105S)	Single nucleotide variant (missense variant +1 more)	NR2F2 associated disorders	GUncertain significance
Select item 2570643	NM_021005.4(NR2F2):c.287G>A (p.Cys96Tyr)	NR2F2 (C96Y)	Single nucleotide variant (missense variant +1 more)	NR2F2 associated disorders	GUncertain significance
Select item 2570642	NM_021005.4(NR2F2):c.933G>C (p.Glu311Asp)	NR2F2 (E178D +2 more)	Single nucleotide variant (missense variant)	NR2F2 associated disorders	GUncertain significance

ClinVar