List of variants in gene NLGN4X reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_181332.3(NLGN4X):c.1877G>A (p.Arg626Gln)	rs1291813149	0.00003
NM_181332.3(NLGN4X):c.2297G>A (p.Arg766Gln)	rs1445553567	0.00001
NM_181332.3(NLGN4X):c.1181A>G (p.Asp394Gly)
NM_181332.3(NLGN4X):c.1216C>A (p.Leu406Ile)	rs886044072
NM_181332.3(NLGN4X):c.1418A>G (p.Tyr473Cys)
NM_181332.3(NLGN4X):c.1477G>A (p.Val493Ile)	rs2031978800
NM_181332.3(NLGN4X):c.1829C>T (p.Thr610Ile)	rs2146686298
NM_181332.3(NLGN4X):c.187C>A (p.Pro63Thr)	rs150566193
NM_181332.3(NLGN4X):c.473-5dup	rs766542143
NM_181332.3(NLGN4X):c.47C>T (p.Pro16Leu)
NM_181332.3(NLGN4X):c.542C>T (p.Thr181Ile)
NM_181332.3(NLGN4X):c.949T>C (p.Cys317Arg)	rs1064797357
NM_181332.3(NLGN4X):c.97G>A (p.Ala33Thr)

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