"Fulgent Genetics, Fulgent Genetics"[submitter] AND "UCP3"[gene] - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1336999	NM_003356.4(UCP3):c.922C>T (p.Arg308Trp)	UCP3 (R308W)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 1029698	NM_003356.4(UCP3):c.490G>A (p.Asp164Asn)	UCP3 (D164N)	Single nucleotide variant (missense variant)	UCP3-related disorder +1 more	GUncertain significance
Select item 1336776	NM_003356.4(UCP3):c.386T>C (p.Met129Thr)	UCP3 (M129T)	Single nucleotide variant (missense variant)	Obesity +1 more	GUncertain significance
Select item 738391	NM_003356.4(UCP3):c.356G>A (p.Arg119Gln)	UCP3 (R119Q)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign
Select item 437205	NM_003356.4(UCP3):c.274G>A (p.Ala92Thr)	UCP3 (A92T)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 426364	NM_003356.4(UCP3):c.202A>G (p.Met68Val)	UCP3 (M68V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 723534	NM_003356.4(UCP3):c.127-7C>T	UCP3	Single nucleotide variant (intron variant)	Obesity +2 more	GBenign/Likely benign
Select item 773827	NM_003356.4(UCP3):c.72C>T (p.Ala24=)	UCP3	Single nucleotide variant (synonymous variant)	Obesity +2 more	GBenign/Likely benign
Select item 1336091	NM_003356.4(UCP3):c.63C>G (p.Gly21=)	UCP3	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign