Related gene-specific medical variations for Gene (Select 84366) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3217989	NM_032391.3(PRAC1):c.63T>A (p.Phe21Leu)	PRAC1, PRAC2 (F21L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3217988	NM_032391.3(PRAC1):c.107A>G (p.Glu36Gly)	PRAC1, PRAC2 (E36G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221712	NM_032391.3(PRAC1):c.72T>A (p.Asn24Lys)	PRAC1, PRAC2 (N24K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 777200	NM_032391.3(PRAC1):c.118G>A (p.Asp40Asn)	PRAC1, PRAC2 (D40N)	Single nucleotide variant (missense variant)	not provided	GBenign

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