Related gene-specific medical variations for Gene (Select 10898) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2491272	NM_006693.4(CPSF4):c.458T>C (p.Val153Ala)	ATP5MF-PTCD1, CPSF4 (V153A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 769333	NM_006693.4(CPSF4):c.483G>A (p.Ser161=)	ATP5MF-PTCD1, CPSF4	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign