List of variants in gene FBXW4 reported as uncertain significance for chromosomal disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_022039.4(FBXW4):c.192G>A (p.Thr64=)	rs886046647	0.00024
NM_022039.4(FBXW4):c.1657G>A (p.Ala553Thr)	rs200476624	0.00021
NM_022039.4(FBXW4):c.*600G>A	rs1022774144	0.00014
NM_022039.4(FBXW4):c.726-12G>T	rs755969920	0.00011
NM_022039.4(FBXW4):c.1465G>A (p.Glu489Lys)	rs770518721	0.00006
NM_022039.4(FBXW4):c.*606A>C	rs886046641	0.00004
NM_022039.4(FBXW4):c.1549C>T (p.Arg517Trp)	rs140286143	0.00003
NM_022039.4(FBXW4):c.1181A>G (p.His394Arg)	rs151048089	0.00001
NM_022039.4(FBXW4):c.*381C>G	rs2063775084
NM_022039.4(FBXW4):c.1170G>T (p.Gly390=)	rs2064322238
NM_022039.4(FBXW4):c.1302-9C>T	rs771930157
NM_022039.4(FBXW4):c.1473C>T (p.His491=)	rs147424741
NM_022039.4(FBXW4):c.316G>T (p.Ala106Ser)	rs2064658916
NM_022039.4(FBXW4):c.923G>A (p.Arg308His)	rs771654851

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