List of variants in gene FBXW7 reported as likely pathogenic for embryonal neoplasm

Minimum submission review status:		Collection method:
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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001349798.2(FBXW7):c.1393C>G (p.Arg465Gly)	rs867384286
NM_001349798.2(FBXW7):c.1393C>T (p.Arg465Cys)	rs867384286
NM_001349798.2(FBXW7):c.1394G>A (p.Arg465His)	rs1057519895
NM_001349798.2(FBXW7):c.1394G>C (p.Arg465Pro)	rs1057519895
NM_001349798.2(FBXW7):c.1394G>T (p.Arg465Leu)	rs1057519895

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