Related gene-specific medical variations for Gene (Select 2339) - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3096158	NM_002027.3(FNTA):c.41G>A (p.Gly14Asp)	FNTA, LOC130000314 (G14D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3096154	NM_002027.3(FNTA):c.22G>A (p.Gly8Arg)	FNTA, LOC130000314 (G8R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2615680	NM_002027.3(FNTA):c.152T>C (p.Met51Thr)	FNTA, LOC130000314 (M51T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2614466	NM_002027.3(FNTA):c.182C>T (p.Pro61Leu)	FNTA, LOC130000314 (P61L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2412389	NM_002027.3(FNTA):c.19G>T (p.Val7Phe)	FNTA, LOC130000314 (V7F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2298618	NM_002027.3(FNTA):c.16G>T (p.Gly6Trp)	FNTA, LOC130000314 (G6W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2257520	NM_002027.3(FNTA):c.157G>C (p.Asp53His)	FNTA, LOC130000314 (D53H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2253011	NM_002027.3(FNTA):c.13G>A (p.Glu5Lys)	FNTA, LOC130000314 (E5K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 783524	NM_002027.3(FNTA):c.190G>A (p.Val64Ile)	FNTA, LOC130000314 (V64I)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign