"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "ZNF107" - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 769718	NM_001282359.2(ZNF107):c.150A>G (p.Pro50=)	ZNF107	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GLikely benign
Select item 709064	NM_001282359.2(ZNF107):c.1027T>G (p.Cys343Gly)	ZNF107 (C343G +4 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 717331	NM_001282359.2(ZNF107):c.1408A>G (p.Asn470Asp)	ZNF107 (N401D +4 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 776231	NM_001282359.2(ZNF107):c.1822C>T (p.Arg608Cys)	ZNF107 (R608C +4 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 713598	NM_001282359.2(ZNF107):c.1954G>A (p.Glu652Lys)	ZNF107 (E620K +4 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 790354	NM_001282359.2(ZNF107):c.2018G>T (p.Gly673Val)	ZNF107 (G604V +4 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 784112	NM_001282359.2(ZNF107):c.2100G>A (p.Thr700=)	ZNF107	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 768151	NM_001282359.2(ZNF107):c.2166A>G (p.Arg722=)	ZNF107	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 786740	NM_001282359.2(ZNF107):c.2217C>T (p.Gly739=)	ZNF107	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 768152	NM_001282359.2(ZNF107):c.2543dup (p.Tyr849fs)	ZNF107 (Y817fs +4 more)	Duplication (frameshift variant)	not provided	GBenign
Select item 768153	NM_001282359.2(ZNF107):c.2544_2545insAA (p.Tyr849fs)	ZNF107 (Y780fs +4 more)	Insertion (frameshift variant)	not provided	GBenign