Related gene-specific medical variations for Gene (Select 283807) - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3278054	NM_001367807.1(FBXL22):c.124G>A (p.Val42Met)	FBXL22, USP3-AS1 (V42M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093535	NM_001367807.1(FBXL22):c.93C>G (p.Ser31Arg)	FBXL22, USP3-AS1 (S31R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093530	NM_001367807.1(FBXL22):c.274C>G (p.Leu92Val)	FBXL22, USP3-AS1 (L92V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093529	NM_001367807.1(FBXL22):c.263T>C (p.Ile88Thr)	FBXL22, USP3-AS1 (I88T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093528	NM_001367807.1(FBXL22):c.121G>A (p.Asp41Asn)	FBXL22, USP3-AS1 (D41N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551787	NM_001367807.1(FBXL22):c.206C>G (p.Pro69Arg)	FBXL22, USP3-AS1 (P69R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482271	NM_001367807.1(FBXL22):c.163C>A (p.Arg55Ser)	FBXL22, USP3-AS1 (R55S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350157	NM_001367807.1(FBXL22):c.281G>A (p.Ser94Asn)	FBXL22, USP3-AS1 (S94N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301284	NM_001367807.1(FBXL22):c.167C>T (p.Ser56Phe)	FBXL22, USP3-AS1 (S56F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268565	NM_001367807.1(FBXL22):c.251A>G (p.Gln84Arg)	FBXL22, USP3-AS1 (Q84R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229638	NM_001367807.1(FBXL22):c.313G>C (p.Glu105Gln)	FBXL22, USP3-AS1 (E105Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204106	NM_001367807.1(FBXL22):c.215G>A (p.Arg72His)	FBXL22, USP3-AS1 (R72H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance