Related gene-specific medical variations for Gene (Select 7352) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3059362	NM_003356.4(UCP3):c.600C>T (p.Tyr200=)	LOC126861261, UCP3	Single nucleotide variant (synonymous variant)	UCP3-related condition	GLikely benign
Select item 3040683	NM_003356.4(UCP3):c.591G>T (p.Val197=)	LOC126861261, UCP3	Single nucleotide variant (synonymous variant)	UCP3-related condition	GLikely benign
Select item 2964481	NM_003356.4(UCP3):c.542-14del	LOC126861261, UCP3	Deletion (intron variant)	not provided	GLikely benign
Select item 2628738	NM_003356.4(UCP3):c.549G>C (p.Leu183Phe)	LOC126861261, UCP3 (L183F)	Single nucleotide variant (missense variant)	UCP3-related condition	GUncertain significance
Select item 2378945	NM_003356.4(UCP3):c.601G>A (p.Asp201Asn)	LOC126861261, UCP3 (D201N)	Single nucleotide variant (missense variant)	UCP3-related condition +1 more	GUncertain significance
Select item 1277076	NM_003356.4(UCP3):c.542-36C>T	LOC126861261, UCP3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1221961	NM_003356.4(UCP3):c.630C>T (p.Tyr210=)	LOC126861261, UCP3	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 727355	NM_003356.4(UCP3):c.643+8C>T	LOC126861261, UCP3	Single nucleotide variant (intron variant)	not provided	GBenign

ClinVar