WWP2[gene] and "single gene"[properties] - ClinVar

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Items: 46

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2517470	NM_001270454.2(WWP2):c.22C>T (p.Arg8Trp)	WWP2 (R8W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333329	NM_001270454.2(WWP2):c.107C>T (p.Pro36Leu)	WWP2 (P36L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2264135	NM_001270454.2(WWP2):c.167C>A (p.Thr56Asn)	WWP2 (T56N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535306	NM_001270454.2(WWP2):c.178A>T (p.Ile60Phe)	WWP2 (I60F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610526	NM_001270454.2(WWP2):c.185G>A (p.Ser62Asn)	WWP2 (S62N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217096	NM_001270454.2(WWP2):c.335G>A (p.Gly112Asp)	WWP2 (G112D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255227	NM_001270454.2(WWP2):c.383A>C (p.Lys128Thr)	WWP2 (K128T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333328	NM_001270454.2(WWP2):c.390C>A (p.Ser130Arg)	WWP2 (S14R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483010	NM_001270454.2(WWP2):c.415A>G (p.Ile139Val)	WWP2 (I139V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466410	NM_001270454.2(WWP2):c.440A>G (p.Asp147Gly)	WWP2 (D147G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355321	NM_001270454.2(WWP2):c.476A>C (p.Asp159Ala)	WWP2 (D43A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349611	NM_001270454.2(WWP2):c.514G>C (p.Ala172Pro)	WWP2 (A56P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 789226	NM_001270454.2(WWP2):c.543C>T (p.Pro181=)	WWP2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2603738	NM_001270454.2(WWP2):c.560T>A (p.Phe187Tyr)	WWP2 (F71Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190916	NM_001270454.2(WWP2):c.574C>T (p.Arg192Trp)	WWP2 (R192W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319061	NM_001270454.2(WWP2):c.590C>G (p.Ser197Trp)	WWP2 (S197W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 722885	NM_001270454.2(WWP2):c.590C>T (p.Ser197Leu)	WWP2 (S197L +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2530785	NM_001270454.2(WWP2):c.708T>A (p.Asn236Lys)	WWP2 (N120K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190917	NM_001270454.2(WWP2):c.725C>A (p.Ala242Asp)	WWP2 (A126D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378796	NM_001270454.2(WWP2):c.748G>A (p.Val250Ile)	WWP2 (V134I +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3190918	NM_001270454.2(WWP2):c.755G>A (p.Gly252Asp)	WWP2 (G136D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516609	NM_001270454.2(WWP2):c.767C>T (p.Pro256Leu)	WWP2 (P256L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243437	NM_001270454.2(WWP2):c.806C>T (p.Thr269Met)	WWP2 (T269M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333327	NM_001270454.2(WWP2):c.835G>A (p.Ala279Thr)	WWP2 (A279T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488722	NM_001270454.2(WWP2):c.865A>G (p.Thr289Ala)	WWP2 (T289A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190919	NM_001270454.2(WWP2):c.938A>G (p.Asn313Ser)	WWP2 (N197S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223296	NM_001270454.2(WWP2):c.944G>A (p.Arg315His)	WWP2 (R199H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317470	NM_001270454.2(WWP2):c.1000C>G (p.Pro334Ala)	WWP2 (P218A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285422	NM_001270454.2(WWP2):c.1199A>G (p.Asp400Gly)	WWP2 (D400G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2308330	NM_001270454.2(WWP2):c.1237A>G (p.Lys413Glu)	WWP2 (K297E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2621202	NM_001270454.2(WWP2):c.1273C>G (p.His425Asp)	WWP2 (H425D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190915	NM_001270454.2(WWP2):c.1393C>T (p.His465Tyr)	WWP2 (H465Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460193	NM_001270454.2(WWP2):c.1430C>T (p.Pro477Leu)	WWP2 (P38L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293202	NM_001270454.2(WWP2):c.1567A>G (p.Thr523Ala)	WWP2 (T407A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547818	NM_001270454.2(WWP2):c.1621C>T (p.Arg541Cys)	WWP2 (R541C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333330	NM_001270454.2(WWP2):c.1723A>G (p.Met575Val)	WWP2 (M136V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2561265	NM_001270454.2(WWP2):c.1860G>T (p.Lys620Asn)	WWP2 (K504N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340789	NM_001270454.2(WWP2):c.2195C>T (p.Ala732Val)	WWP2 (A293V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290675	NM_001270454.2(WWP2):c.2216A>G (p.Tyr739Cys)	WWP2 (Y300C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333326	NM_001270454.2(WWP2):c.2273G>A (p.Ser758Asn)	WWP2 (S758N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621099	NM_001270454.2(WWP2):c.2309C>G (p.Thr770Ser)	WWP2 (T331S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346880	NM_001270454.2(WWP2):c.2331G>C (p.Gln777His)	WWP2 (Q661H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300298	NM_001270454.2(WWP2):c.2331G>T (p.Gln777His)	WWP2 (Q661H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540996	NM_001270454.2(WWP2):c.2438T>C (p.Ile813Thr)	WWP2 (I374T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206725	NM_001270454.2(WWP2):c.2483A>G (p.Lys828Arg)	WWP2 (K828R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 685807	GRCh37/hg19 16q22.1(chr16:69814610-69941373)x1	WWP2	Copy number loss	not provided	GUncertain significance

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Items: 46