"Ambry Genetics"[submitter] AND "LOC100506235"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1164883	NM_001190274.2(FBXO11):c.149A>C (p.Gln50Pro)	FBXO11, LOC100506235 (Q50P)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GBenign/Likely benign
Select item 1532921	NM_001190274.2(FBXO11):c.105GCCCCAGCAGCAGCC[3] (p.37QQQPP[3])	FBXO11, LOC100506235	Microsatellite (inframe_insertion)	Inborn genetic diseases +1 more	GLikely benign
Select item 1078575	NM_001190274.2(FBXO11):c.105GCCCCAGCAGCAGCC[1] (p.37QQQPP[1])	FBXO11, LOC100506235	Microsatellite (inframe_deletion)	Inborn genetic diseases +1 more	GBenign/Likely benign
Select item 975696	NM_001190274.2(FBXO11):c.96_107del (p.Pro33_Pro36del)	FBXO11, LOC100506235	Deletion (inframe_deletion)	Inborn genetic diseases +1 more	GLikely benign
Select item 2250800	NM_001190274.2(FBXO11):c.86A>G (p.Gln29Arg)	FBXO11, LOC100506235 (Q29R)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1167516	NM_001190274.2(FBXO11):c.68AGC[5] (p.Gln26dup)	FBXO11, LOC100506235	Microsatellite (inframe_insertion)	Inborn genetic diseases +1 more	GBenign/Likely benign
Select item 2532699	NM_001190274.2(FBXO11):c.66_71del (p.Gln25_Gln26del)	FBXO11, LOC100506235	Deletion (non-coding transcript variant)	Inborn genetic diseases	GLikely benign

ClinVar