"PreventionGenetics, part of Exact Sciences"[submitter] AND "FBXO31"[g - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 708552	NM_024735.5(FBXO31):c.1397+10C>T	FBXO31	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 2631976	NM_024735.5(FBXO31):c.1133G>A (p.Arg378His)	FBXO31 (R206H +1 more)	Single nucleotide variant (missense variant)	FBXO31-related disorder	GUncertain significance
Select item 3053211	NM_024735.5(FBXO31):c.996+9C>T	FBXO31	Single nucleotide variant (intron variant)	FBXO31-related disorder	GLikely benign
Select item 3047823	NM_024735.5(FBXO31):c.543C>T (p.His181=)	FBXO31	Single nucleotide variant (synonymous variant)	FBXO31-related disorder	GLikely benign
Select item 2630576	NM_024735.5(FBXO31):c.496G>A (p.Gly166Ser)	FBXO31 (G166S)	Single nucleotide variant (5 prime UTR variant +1 more)	FBXO31-related disorder	GUncertain significance
Select item 3045547	NM_024735.5(FBXO31):c.495C>T (p.Asp165=)	FBXO31	Single nucleotide variant (5 prime UTR variant +1 more)	FBXO31-related disorder	GLikely benign
Select item 721910	NM_024735.5(FBXO31):c.432C>T (p.His144=)	FBXO31	Single nucleotide variant (5 prime UTR variant +1 more)	FBXO31-related disorder +1 more	GLikely benign
Select item 730498	NM_024735.5(FBXO31):c.322A>C (p.Arg108=)	FBXO31	Single nucleotide variant (synonymous variant +1 more)	FBXO31-related disorder +2 more	GLikely benign
Select item 2633219	NM_024735.5(FBXO31):c.85G>A (p.Ala29Thr)	FBXO31 (A29T)	Single nucleotide variant (missense variant +1 more)	FBXO31-related disorder	GUncertain significance
Select item 784345	NM_024735.5(FBXO31):c.84G>C (p.Thr28=)	FBXO31	Single nucleotide variant (synonymous variant +1 more)	FBXO31-related disorder +1 more	GBenign