"Ambry Genetics"[submitter] AND "STK25"[gene] - ClinVar

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Items: 33

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 +1 more	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 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 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 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 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 2316074	NM_014808.4(FARP2):c.3044A>G (p.Glu1015Gly)	FARP2, STK25 (E1015G)	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 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 2387473	NM_001271977.2(STK25):c.1277G>A (p.Arg426His)	STK25 (R426H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385933	NM_001271977.2(STK25):c.1276C>T (p.Arg426Cys)	STK25 (R332C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493045	NM_001271977.2(STK25):c.1230G>T (p.Glu410Asp)	STK25 (E336D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293193	NM_001271977.2(STK25):c.1093G>A (p.Val365Ile)	STK25 (V288I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467973	NM_001271977.2(STK25):c.1087C>T (p.Arg363Trp)	STK25 (R286W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171309	NM_001271977.2(STK25):c.1045G>A (p.Val349Ile)	STK25 (V275I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281163	NM_001271977.2(STK25):c.1034C>T (p.Pro345Leu)	STK25 (P268L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255795	NM_001271977.2(STK25):c.1021A>G (p.Ser341Gly)	STK25 (S267G +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2480932	NM_001271977.2(STK25):c.976C>T (p.Arg326Trp)	STK25 (R326W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171317	NM_001271977.2(STK25):c.967C>G (p.Pro323Ala)	STK25 (P323A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2475257	NM_001271977.2(STK25):c.953T>G (p.Ile318Ser)	STK25 (I224S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171316	NM_001271977.2(STK25):c.932A>C (p.Glu311Ala)	STK25 (E234A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171315	NM_001271977.2(STK25):c.929C>T (p.Ala310Val)	STK25 (A216V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171314	NM_001271977.2(STK25):c.875C>T (p.Ser292Leu)	STK25 (S215L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171313	NM_001271977.2(STK25):c.865C>T (p.Arg289Cys)	STK25 (R212C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171312	NM_001271977.2(STK25):c.856C>T (p.Arg286Cys)	STK25 (R212C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171311	NM_001271977.2(STK25):c.767G>A (p.Arg256Gln)	STK25 (R179Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304166	NM_001271977.2(STK25):c.764C>T (p.Pro255Leu)	STK25 (P161L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171310	NM_001271977.2(STK25):c.577G>A (p.Asp193Asn)	STK25 (D193N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476805	NM_001271977.2(STK25):c.386A>G (p.Asp129Gly)	STK25 (D35G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283014	NM_001271977.2(STK25):c.301G>A (p.Gly101Ser)	STK25 (G7S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612766	NM_001271977.2(STK25):c.154G>A (p.Asp52Asn)	STK25 (D52N)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2479846	NM_001271977.2(STK25):c.23C>T (p.Ala8Val)	STK25 (A8V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3323290	NM_001271977.2(STK25):c.9C>G (p.His3Gln)	STK25 (H3Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

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Items: 33