"Genetic Services Laboratory, University of Chicago"[submitter] AND "N - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 211682	NM_181332.3(NLGN4X):c.2361G>A (p.Thr787=)	NLGN4X	Single nucleotide variant (synonymous variant)	not specified	GUncertain significance
Select item 211681	NM_181332.3(NLGN4X):c.2360C>T (p.Thr787Met)	NLGN4X (T787M)	Single nucleotide variant (missense variant)	Autism, susceptibility to, X-linked 2 +3 more	GConflicting classifications of pathogenicity
Select item 95982	NM_181332.3(NLGN4X):c.2271G>A (p.Pro757=)	NLGN4X	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign
Select item 436022	NM_181332.3(NLGN4X):c.2128C>T (p.Arg710Cys)	NLGN4X (R710C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 211680	NM_181332.3(NLGN4X):c.1887C>T (p.Pro629=)	NLGN4X	Single nucleotide variant (synonymous variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 95981	NM_181332.3(NLGN4X):c.1779C>G (p.Leu593=)	NLGN4X	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign
Select item 95980	NM_181332.3(NLGN4X):c.1777C>T (p.Leu593Phe)	NLGN4X (L593F)	Single nucleotide variant (missense variant)	Autism, susceptibility to, X-linked 2 +3 more	GBenign/Likely benign
Select item 436020	NM_181332.3(NLGN4X):c.1380C>T (p.His460=)	NLGN4X	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 95977	NM_181332.3(NLGN4X):c.1251G>C (p.Arg417=)	NLGN4X	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +1 more	GBenign
Select item 436021	NM_181332.3(NLGN4X):c.955C>A (p.Arg319=)	NLGN4X	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +2 more	GBenign/Likely benign
Select item 95987	NM_181332.3(NLGN4X):c.933C>T (p.Thr311=)	NLGN4X	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 196500	NM_181332.3(NLGN4X):c.591C>T (p.Ile197=)	NLGN4X	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +5 more	GBenign/Likely benign
Select item 95976	NM_181332.3(NLGN4X):c.115A>G (p.Ile39Val)	NLGN4X (I39V)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 129805	NM_181332.3(NLGN4X):c.54C>T (p.Cys18=)	NLGN4X	Single nucleotide variant (synonymous variant)	not specified	GBenign