FUOM[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 2369398	NM_001098483.3(FUOM):c.436G>A (p.Gly146Arg)	FUOM (G101R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2353365	NM_001098483.3(FUOM):c.436G>C (p.Gly146Arg)	FUOM (G101R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2276317	NM_001098483.3(FUOM):c.394A>G (p.Thr132Ala)	FUOM (T87A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2477373	NM_001098483.3(FUOM):c.386T>C (p.Val129Ala)	FUOM (V84A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404684	NM_001098483.3(FUOM):c.364C>T (p.Arg122Trp)	FUOM (R99W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2236450	NM_001098483.3(FUOM):c.357T>A (p.Phe119Leu)	FUOM (F119L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280173	NM_001098483.3(FUOM):c.337A>G (p.Lys113Glu)	FUOM (K68E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097449	NM_001098483.3(FUOM):c.281T>C (p.Val94Ala)	FUOM (V94A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623916	NM_001098483.3(FUOM):c.266G>T (p.Gly89Val)	FUOM (G44V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097448	NM_001098483.3(FUOM):c.245T>C (p.Val82Ala)	FUOM (V82A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2266238	NM_001098483.3(FUOM):c.116C>T (p.Ser39Phe)	FUOM (S39F)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance