Related gene-specific medical variations for Gene (Select 25874) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3295645	NM_001143674.4(MPC2):c.202A>C (p.Ser68Arg)	DCAF6, MPC2 (S68R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2604354	NM_001198956.2(DCAF6):c.71C>T (p.Pro24Leu)	DCAF6, LOC129931878 +1 more (P24L)	Single nucleotide variant (5 prime UTR variant +3 more)	not specified	GUncertain significance
Select item 2290824	NM_001143674.4(MPC2):c.31G>C (p.Ala11Pro)	DCAF6, MPC2 (A11P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2270029	NM_001143674.4(MPC2):c.257C>T (p.Ser86Leu)	DCAF6, MPC2 (S86L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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