FBXO36[gene] and "single gene"[properties] - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2205552	NM_174899.5(FBXO36):c.107G>C (p.Arg36Thr)	FBXO36 (R36T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093699	NM_174899.5(FBXO36):c.140G>A (p.Arg47Gln)	FBXO36 (R47Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2651989	NM_174899.5(FBXO36):c.151C>T (p.Pro51Ser)	FBXO36 (P51S)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2354530	NM_174899.5(FBXO36):c.173A>G (p.His58Arg)	FBXO36 (H58R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543093	NM_174899.5(FBXO36):c.193T>G (p.Ser65Ala)	FBXO36 (S65A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366788	NM_174899.5(FBXO36):c.245A>G (p.Tyr82Cys)	FBXO36 (Y82C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487154	NM_174899.5(FBXO36):c.426C>G (p.Cys142Trp)	FBXO36 (C142W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514571	NM_174899.5(FBXO36):c.446T>C (p.Val149Ala)	FBXO36 (V149A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353465	NM_174899.5(FBXO36):c.521G>A (p.Arg174His)	FBXO36 (R174H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482086	NM_174899.5(FBXO36):c.551G>A (p.Arg184Lys)	FBXO36 (R184K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance