"PreventionGenetics, part of Exact Sciences"[submitter] AND "NOL3"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3055509	NM_001276309.3(NOL3):c.-8-132C>T	NOL3	Single nucleotide variant (5 prime UTR variant +1 more)	NOL3-related disorder	GBenign
Select item 3058233	NM_001276309.3(NOL3):c.-4G>T	NOL3	Single nucleotide variant (5 prime UTR variant)	NOL3-related disorder	GLikely benign
Select item 3050129	NM_001276309.3(NOL3):c.75G>A (p.Ala25=)	NOL3	Single nucleotide variant (synonymous variant)	NOL3-related disorder	GBenign
Select item 3047843	NM_001276309.3(NOL3):c.76G>T (p.Asp26Tyr)	NOL3 (D26Y)	Single nucleotide variant (missense variant)	NOL3-related disorder	GLikely benign
Select item 3040437	NM_001276309.3(NOL3):c.408C>G (p.Ala136=)	NOL3 (P133R +1 more)	Single nucleotide variant (missense variant +1 more)	NOL3-related disorder	GLikely benign
Select item 2632778	NM_001276309.3(NOL3):c.547C>T (p.Pro183Ser)	NOL3 (P183S)	Single nucleotide variant (synonymous variant +1 more)	NOL3-related disorder	GUncertain significance
Select item 3053872	NM_001276309.3(NOL3):c.*22G>T	NOL3	Single nucleotide variant (synonymous variant +1 more)	NOL3-related disorder	GLikely benign
Select item 3051480	NM_001276309.3(NOL3):c.*50G>A	NOL3	Single nucleotide variant (3 prime UTR variant)	NOL3-related disorder	GBenign

ClinVar