List of variants in gene FBXW4, LOC130004563 studied for chromosome 10 disorder

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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_022039.4(FBXW4):c.461T>A (p.Val154Glu)	rs61382490	0.15406
NM_022039.4(FBXW4):c.534C>G (p.Ala178=)	rs61761937	0.03084
NM_022039.4(FBXW4):c.440C>A (p.Ala147Asp)	rs117664315	0.02439
NM_022039.4(FBXW4):c.472G>C (p.Ala158Pro)	rs111600818	0.01363
NM_022039.4(FBXW4):c.710G>A (p.Arg237Gln)	rs886046642	0.00001
NM_022039.4(FBXW4):c.409A>G (p.Arg137Gly)	rs886046645
NM_022039.4(FBXW4):c.437G>A (p.Trp146Ter)	rs886046644
NM_022039.4(FBXW4):c.493G>A (p.Glu165Lys)	rs886046643
NM_022039.4(FBXW4):c.507G>A (p.Ala169=)	rs1404824736
NM_022039.4(FBXW4):c.715G>A (p.Gly239Ser)	rs759941552

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