"GeneDx"[submitter] AND "UCP3"[gene] - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58916	GRCh38/hg38 11q13.4-13.5(chr11:71928796-77064521)x1	LOC130006424, LOC130006425 +305 more	Copy number loss	See cases	GPathogenic
Select item 58917	GRCh38/hg38 11q13.4-14.1(chr11:71969881-78232895)x1	AAMDC, ACER3 +355 more	Copy number loss	See cases	GPathogenic
Select item 1286622	NM_003356.4(UCP3):c.825-149GA[7]	UCP3	Microsatellite (intron variant)	not provided	GBenign
Select item 1179763	NM_003356.4(UCP3):c.825-208dup	UCP3	Duplication (intron variant)	not provided	GBenign
Select item 1254088	NM_003356.4(UCP3):c.825-288A>G	UCP3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1277754	NM_003356.4(UCP3):c.824+533C>T	UCP3	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign
Select item 7578	NM_003356.4(UCP3):c.824+1G>A	UCP3	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1221961	NM_003356.4(UCP3):c.630C>T (p.Tyr210=)	LOC126861261, UCP3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1277076	NM_003356.4(UCP3):c.542-36C>T	LOC126861261, UCP3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1178598	NM_003356.4(UCP3):c.338-46T>A	UCP3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1258033	NM_003356.4(UCP3):c.338-47A>G	UCP3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1267154	NM_003356.4(UCP3):c.297T>C (p.Tyr99=)	UCP3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 426364	NM_003356.4(UCP3):c.202A>G (p.Met68Val)	UCP3 (M68V)	Single nucleotide variant (missense variant)	Obesity +1 more	GUncertain significance
Select item 1181566	NM_003356.4(UCP3):c.127-143G>C	UCP3	Single nucleotide variant (intron variant)	not provided	GBenign