List of variants in gene FBXO31 studied for autosomal recessive non-syndromic intellectual disability

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_024735.5(FBXO31):c.996+4A>G	rs765703905	0.00003
NM_024735.5(FBXO31):c.1000G>A (p.Asp334Asn)	rs2150668444
NM_024735.5(FBXO31):c.1348G>A (p.Val450Met)	rs145589459
NM_024735.5(FBXO31):c.44G>A (p.Gly15Glu)	rs1235563636
NM_024735.5(FBXO31):c.638C>A (p.Pro213His)	rs1905261526
NM_024735.5(FBXO31):c.842+1G>A
NM_024735.5(FBXO31):c.847_852delinsA (p.Cys283fs)	rs587777703

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