Related gene-specific medical variations for Gene (Select 1347) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2608876	NM_001865.6(COX7A2):c.-77A>G	COX7A2, LOC129996731	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2334756	NM_001865.6(COX7A2):c.-90A>T	COX7A2, LOC129996731	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2326123	NM_001865.6(COX7A2):c.-80C>T	COX7A2, LOC129996731	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2238994	NM_001366293.2(COX7A2):c.8G>A (p.Arg3Gln)	COX7A2, LOC129996731 (R3Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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