FBXL20[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3093526	NM_032875.3(FBXL20):c.1148G>A (p.Arg383Gln)	FBXL20 (R385Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217620	NM_032875.3(FBXL20):c.1139G>A (p.Ser380Asn)	FBXL20 (S417N +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368531	NM_032875.3(FBXL20):c.985G>A (p.Val329Ile)	FBXL20 (V297I +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461063	NM_032875.3(FBXL20):c.728G>T (p.Cys243Phe)	FBXL20 (C211F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093527	NM_032875.3(FBXL20):c.657C>G (p.His219Gln)	FBXL20 (H189Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518513	NM_032875.3(FBXL20):c.646A>G (p.Ile216Val)	FBXL20 (I186V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2266491	NM_032875.3(FBXL20):c.617C>T (p.Thr206Met)	FBXL20 (T208M +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487264	NM_032875.3(FBXL20):c.522G>T (p.Leu174Phe)	FBXL20 (L142F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382932	NM_032875.3(FBXL20):c.320A>G (p.Asn107Ser)	FBXL20 (N107S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2471444	NM_032875.3(FBXL20):c.239G>A (p.Arg80Gln)	FBXL20 (R80Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093525	NM_032875.3(FBXL20):c.103C>T (p.Arg35Trp)	FBXL20 (R35W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance