Related gene-specific medical variations for Gene (Select 150684) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3147907	NM_152516.4(COMMD1):c.74A>G (p.His25Arg)	COMMD1, LOC129933847 (H25R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2546230	NM_006430.4(CCT4):c.59G>A (p.Gly20Glu)	CCT4, COMMD1 (G20E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2400552	NM_006430.4(CCT4):c.71A>T (p.Tyr24Phe)	CCT4, COMMD1 (Y24F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2391851	NM_152516.4(COMMD1):c.83C>T (p.Pro28Leu)	COMMD1, LOC129933847 (P28L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2285540	NM_152516.4(COMMD1):c.116T>C (p.Leu39Pro)	COMMD1, LOC129933847 (L39P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 688228	GRCh37/hg19 2p15(chr2:62195677-62228180)x1	COMMD1	Copy number loss	not provided	GUncertain significance

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