"Ambry Genetics"[submitter] AND "FBXO31"[gene] - ClinVar

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Search results

Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2270794	NM_024735.5(FBXO31):c.1504G>C (p.Glu502Gln)	FBXO31 (E330Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093666	NM_024735.5(FBXO31):c.1348G>T (p.Val450Leu)	FBXO31 (V278L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093665	NM_024735.5(FBXO31):c.1339G>A (p.Val447Met)	FBXO31 (V275M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369571	NM_024735.5(FBXO31):c.1298C>A (p.Ala433Glu)	FBXO31 (A261E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524787	NM_024735.5(FBXO31):c.1252G>A (p.Gly418Arg)	FBXO31 (G246R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093663	NM_024735.5(FBXO31):c.1175G>A (p.Arg392His)	FBXO31 (R392H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208910	NM_024735.5(FBXO31):c.1153G>A (p.Gly385Arg)	FBXO31 (G385R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528380	NM_024735.5(FBXO31):c.1048C>T (p.His350Tyr)	FBXO31 (H178Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093668	NM_024735.5(FBXO31):c.884G>A (p.Arg295His)	FBXO31 (R295H +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3093667	NM_024735.5(FBXO31):c.875C>T (p.Pro292Leu)	FBXO31 (P292L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354335	NM_024735.5(FBXO31):c.669G>T (p.Lys223Asn)	FBXO31 (K223N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204345	NM_024735.5(FBXO31):c.646G>A (p.Gly216Ser)	FBXO31 (G44S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304545	NM_024735.5(FBXO31):c.634G>A (p.Gly212Arg)	FBXO31 (G40R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344559	NM_024735.5(FBXO31):c.598A>G (p.Lys200Glu)	FBXO31 (K200E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494188	NM_024735.5(FBXO31):c.508A>G (p.Ile170Val)	FBXO31 (I170V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2557019	NM_024735.5(FBXO31):c.432C>G (p.His144Gln)	FBXO31 (H144Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2404662	NM_024735.5(FBXO31):c.326G>A (p.Arg109Lys)	FBXO31 (R109K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2612022	NM_024735.5(FBXO31):c.238G>T (p.Ala80Ser)	FBXO31 (A80S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2550103	NM_024735.5(FBXO31):c.133G>C (p.Glu45Gln)	FBXO31 (E45Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3093664	NM_024735.5(FBXO31):c.132C>G (p.Ile44Met)	FBXO31 (I44M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2592292	NM_024735.5(FBXO31):c.59A>C (p.Gln20Pro)	FBXO31 (Q20P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2275423	NM_024735.5(FBXO31):c.59A>G (p.Gln20Arg)	FBXO31 (Q20R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2378770	NM_024735.5(FBXO31):c.58C>A (p.Gln20Lys)	FBXO31 (Q20K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2508897	NM_024735.5(FBXO31):c.35C>A (p.Pro12Gln)	FBXO31 (P12Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2245858	NM_024735.5(FBXO31):c.29T>G (p.Val10Gly)	FBXO31 (V10G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 25