"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "ZNF141" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 771138	NM_003441.4(ZNF141):c.370A>G (p.Lys124Glu)	ZNF141 (K48E +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 718907	NM_003441.4(ZNF141):c.386G>A (p.Gly129Asp)	ZNF141 (G129D +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 721178	NM_003441.4(ZNF141):c.487C>T (p.Arg163Cys)	ZNF141 (R163C +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 714237	NM_003441.4(ZNF141):c.1179A>G (p.Lys393=)	ZNF141	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 715929	NM_003441.4(ZNF141):c.1419T>C (p.His473=)	ZNF141	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1511339	NC_000004.11:g.(?_124553)_(502759_?)dup	PIGG, ZNF141 +3 more	Duplication	Intellectual disability, autosomal recessive 53	GUncertain significance
Select item 1056004	NC_000004.11:g.(?_264888)_(682916_?)dup	ATP5ME, MYL5 +6 more	Duplication	not provided	GUncertain significance

ClinVar