List of variants in gene ARX reported by Institute of Human Genetics, University of Leipzig Medical Center

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_139058.3(ARX):c.1058C>T (p.Pro353Leu)	rs104894743
NM_139058.3(ARX):c.1105G>A (p.Glu369Lys)	rs104894746
NM_139058.3(ARX):c.1128C>G (p.Phe376Leu)	rs2048683301
NM_139058.3(ARX):c.1522G>A (p.Val508Met)	rs2048670414
NM_139058.3(ARX):c.1546G>T (p.Ala516Ser)	rs747042039
NM_139058.3(ARX):c.1684T>C (p.Cys562Arg)	rs2048668859
NM_139058.3(ARX):c.946G>A (p.Gly316Ser)	rs2048708756
NM_139058.3(ARX):c.989G>A (p.Arg330His)	rs886039308

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