Related gene-specific medical variations for Gene (Select 254170) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2490229	NM_203301.4(FBXO33):c.119G>A (p.Gly40Glu)	FBXO33, LOC130055513 (G40E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2253476	NM_203301.4(FBXO33):c.58G>C (p.Gly20Arg)	FBXO33, LOC130055513 (G20R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1807685	GRCh37/hg19 14q21.1(chr14:39775264-39984089)x1	FBXO33	Copy number loss	not provided	GUncertain significance
Select item 1340767	GRCh37/hg19 14q21.1(chr14:39778566-39984043)x1	FBXO33	Copy number loss	not provided	GUncertain significance
Select item 815646	GRCh37/hg19 14q21.1(chr14:39876467-40091340)x3	FBXO33	Copy number gain	not provided	GUncertain significance
Select item 770425	NM_203301.4(FBXO33):c.101_109del (p.Gln34_Arg36del)	FBXO33, LOC130055513	Deletion (inframe_deletion)	not provided	GBenign

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