List of variants in gene FBXO11 reported as pathogenic by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001190274.2(FBXO11):c.1537G>T (p.Gly513Ter)
NM_001190274.2(FBXO11):c.2224C>T (p.Arg742Ter)	rs2104657995
NM_001190274.2(FBXO11):c.2327del (p.Gly776fs)
NM_001190274.2(FBXO11):c.602_603insCGATATATATATCCTGATATATATATATATCA (p.Met201fs)	rs1672531686

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