Related gene-specific medical variations for Gene (Select 9855) - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3092902	NM_014808.4(FARP2):c.3023C>T (p.Ala1008Val)	FARP2, STK25 (A1008V)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2652114	NM_014808.4(FARP2):c.3159G>A (p.Glu1053=)	FARP2, STK25	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2496410	NM_014808.4(FARP2):c.2854G>A (p.Val952Ile)	FARP2, STK25 (V952I)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2484415	NM_014808.4(FARP2):c.3070G>A (p.Ala1024Thr)	FARP2, STK25 (A1024T)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2455987	NM_014808.4(FARP2):c.2956G>A (p.Ala986Thr)	FARP2, STK25 (A986T)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2356558	NM_014808.4(FARP2):c.3097A>G (p.Ser1033Gly)	FARP2, STK25 (S1033G)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2329254	NM_014808.4(FARP2):c.2930G>A (p.Gly977Asp)	FARP2, STK25 (G977D)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2316074	NM_014808.4(FARP2):c.3044A>G (p.Glu1015Gly)	STK25, FARP2 (E1015G)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2307980	NM_014808.4(FARP2):c.2882A>G (p.Tyr961Cys)	FARP2, STK25 (Y961C)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2305151	NM_014808.4(FARP2):c.2968C>A (p.His990Asn)	FARP2, STK25 (H990N)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 785028	NM_014808.4(FARP2):c.3027G>A (p.Glu1009=)	FARP2, STK25	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 722356	NM_014808.4(FARP2):c.3138G>A (p.Glu1046=)	FARP2, STK25	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign