FBXO9[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3093814	NM_033480.3(FBXO9):c.4-6C>G	FBXO9 (P10A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2241001	NM_033480.3(FBXO9):c.77A>C (p.Glu26Ala)	FBXO9 (E36A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2252299	NM_033480.3(FBXO9):c.124T>G (p.Phe42Val)	FBXO9 (F52V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278214	NM_033480.3(FBXO9):c.169C>A (p.Pro57Thr)	FBXO9 (P23T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265375	NM_033480.3(FBXO9):c.191C>T (p.Ser64Phe)	FBXO9 (S30F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204178	NM_033480.3(FBXO9):c.254G>A (p.Arg85Gln)	FBXO9 (R85Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536955	NM_033480.3(FBXO9):c.350T>C (p.Ile117Thr)	FBXO9 (I83T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093815	NM_033480.3(FBXO9):c.394G>A (p.Val132Ile)	FBXO9 (V132I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385798	NM_033480.3(FBXO9):c.455A>G (p.Tyr152Cys)	FBXO9 (Y118C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093816	NM_033480.3(FBXO9):c.505C>T (p.Pro169Ser)	FBXO9 (P135S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533760	NM_033480.3(FBXO9):c.586A>C (p.Ser196Arg)	FBXO9 (S162R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093817	NM_033480.3(FBXO9):c.671G>A (p.Arg224His)	FBXO9 (R224H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216694	NM_033480.3(FBXO9):c.758G>A (p.Arg253His)	FBXO9 (R219H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093813	NM_033480.3(FBXO9):c.1065C>G (p.Asp355Glu)	FBXO9 (D355E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296172	NM_033480.3(FBXO9):c.1210A>G (p.Thr404Ala)	FBXO9 (T414A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance