Related gene-specific medical variations for Gene (Select 286097) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2392772	NM_181723.3(MICU3):c.154G>A (p.Ala52Thr)	LOC129999927, MICU3 (A52T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2385469	NM_181723.3(MICU3):c.259G>C (p.Gly87Arg)	LOC129999927, MICU3 (G87R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2358694	NM_181723.3(MICU3):c.290G>A (p.Gly97Glu)	LOC129999927, MICU3 (G97E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2354096	NM_181723.3(MICU3):c.192G>C (p.Trp64Cys)	LOC129999927, MICU3 (W64C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2204483	NM_181723.3(MICU3):c.157G>A (p.Val53Met)	LOC129999927, MICU3 (V53M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2203916	NM_181723.3(MICU3):c.196G>C (p.Glu66Gln)	LOC129999927, MICU3 (E66Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 563424	GRCh37/hg19 8p22(chr8:16873493-16927378)x1	MICU3	Copy number loss	not provided	GUncertain significance

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