"Fulgent Genetics, Fulgent Genetics"[submitter] AND "UCP2"[gene] - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 437198	NM_003355.3(UCP2):c.803C>G (p.Ala268Gly)	UCP2 (A268G +2 more)	Single nucleotide variant (missense variant)	not provided +2 more	GLikely benign
Select item 1338586	NM_003355.3(UCP2):c.799C>T (p.Arg267Ter)	UCP2 (R202* +2 more)	Single nucleotide variant (nonsense)	Body mass index quantitative trait locus 4 +1 more	GUncertain significance
Select item 130696	NM_003355.3(UCP2):c.750C>T (p.Tyr250=)	UCP2	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign
Select item 437199	NM_003355.3(UCP2):c.227G>A (p.Arg76Gln)	UCP2 (R76Q)	Single nucleotide variant (missense variant)	Body mass index quantitative trait locus 4 +2 more	GBenign/Likely benign
Select item 437204	NM_003355.3(UCP2):c.79G>A (p.Ala27Thr)	UCP2 (A27T)	Single nucleotide variant (missense variant)	Body mass index quantitative trait locus 4 +2 more	GUncertain significance

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