WWC2[gene] and "single gene"[properties] - ClinVar

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Items: 63

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2237935	NM_024949.6(WWC2):c.8G>A (p.Arg3Lys)	WWC2 (R3K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286906	NM_024949.6(WWC2):c.170A>C (p.Asp57Ala)	WWC2 (D57A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261794	NM_024949.6(WWC2):c.326A>T (p.Asp109Val)	WWC2 (D109V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301493	NM_024949.6(WWC2):c.397G>A (p.Val133Met)	WWC2 (V133M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205946	NM_024949.6(WWC2):c.617T>A (p.Met206Lys)	WWC2 (M206K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515284	NM_024949.6(WWC2):c.817T>A (p.Ser273Thr)	WWC2 (S273T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293092	NM_024949.6(WWC2):c.935A>G (p.Tyr312Cys)	WWC2 (Y312C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190881	NM_024949.6(WWC2):c.937G>A (p.Glu313Lys)	WWC2 (E313K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621637	NM_024949.6(WWC2):c.980C>T (p.Ser327Leu)	WWC2 (S327L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190882	NM_024949.6(WWC2):c.997G>A (p.Ala333Thr)	WWC2 (A333T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190865	NM_024949.6(WWC2):c.1021G>A (p.Glu341Lys)	WWC2 (E341K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376468	NM_024949.6(WWC2):c.1081G>A (p.Val361Ile)	WWC2 (V361I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614415	NM_024949.6(WWC2):c.1087C>T (p.Pro363Ser)	WWC2 (P363S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190866	NM_024949.6(WWC2):c.1096C>T (p.Arg366Cys)	WWC2 (R366C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2568944	NM_024949.6(WWC2):c.1126G>T (p.Ala376Ser)	WWC2 (A376S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313576	NM_024949.6(WWC2):c.1133G>A (p.Arg378Lys)	WWC2 (R378K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552067	NM_024949.6(WWC2):c.1138C>T (p.Arg380Trp)	WWC2 (R380W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401522	NM_024949.6(WWC2):c.1192G>A (p.Glu398Lys)	WWC2 (E398K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 780936	NM_024949.6(WWC2):c.1468C>T (p.Leu490=)	WWC2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2212654	NM_024949.6(WWC2):c.1484G>T (p.Gly495Val)	WWC2 (G495V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534151	NM_024949.6(WWC2):c.1493C>A (p.Pro498His)	WWC2 (P498H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618703	NM_024949.6(WWC2):c.1514T>C (p.Ile505Thr)	WWC2 (I505T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401362	NM_024949.6(WWC2):c.1548G>T (p.Gln516His)	WWC2 (Q516H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536793	NM_024949.6(WWC2):c.1570G>C (p.Gly524Arg)	WWC2 (G524R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284396	NM_024949.6(WWC2):c.1790T>C (p.Ile597Thr)	WWC2 (I597T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190868	NM_024949.6(WWC2):c.1819G>C (p.Asp607His)	WWC2 (D607H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306023	NM_024949.6(WWC2):c.1864G>T (p.Asp622Tyr)	WWC2 (D622Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289966	NM_024949.6(WWC2):c.1868T>C (p.Leu623Pro)	WWC2 (L623P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190869	NM_024949.6(WWC2):c.1912G>T (p.Val638Leu)	WWC2 (V638L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355580	NM_024949.6(WWC2):c.1939G>A (p.Val647Met)	WWC2 (V647M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334797	NM_024949.6(WWC2):c.2086A>G (p.Ile696Val)	WWC2 (I696V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2617096	NM_024949.6(WWC2):c.2111T>C (p.Ile704Thr)	WWC2 (I704T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536669	NM_024949.6(WWC2):c.2134A>G (p.Ser712Gly)	WWC2 (S712G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245595	NM_024949.6(WWC2):c.2204A>C (p.Lys735Thr)	WWC2 (K735T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373890	NM_024949.6(WWC2):c.2239A>G (p.Thr747Ala)	WWC2 (T747A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2610328	NM_024949.6(WWC2):c.2335T>G (p.Leu779Val)	WWC2 (L779V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 755128	NM_024949.6(WWC2):c.2346G>A (p.Lys782=)	WWC2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3190870	NM_024949.6(WWC2):c.2396G>T (p.Cys799Phe)	WWC2 (C799F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297973	NM_024949.6(WWC2):c.2401G>T (p.Ala801Ser)	WWC2 (A801S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190871	NM_024949.6(WWC2):c.2455C>G (p.Leu819Val)	WWC2 (L819V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190873	NM_024949.6(WWC2):c.2561T>C (p.Leu854Ser)	WWC2 (L854S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190874	NM_024949.6(WWC2):c.2585C>G (p.Ala862Gly)	WWC2 (A862G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190875	NM_024949.6(WWC2):c.2617C>A (p.Gln873Lys)	WWC2 (Q873K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190876	NM_024949.6(WWC2):c.2662C>A (p.Pro888Thr)	WWC2 (P888T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2568945	NM_024949.6(WWC2):c.2834A>G (p.Asn945Ser)	WWC2 (N969S +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3190877	NM_024949.6(WWC2):c.2917A>G (p.Asn973Asp)	WWC2 (N973D +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2347540	NM_024949.6(WWC2):c.2920G>A (p.Asp974Asn)	WWC2 (D974N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190878	NM_024949.6(WWC2):c.3028C>T (p.Arg1010Trp)	WWC2 (R1034W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346927	NM_024949.6(WWC2):c.3100G>A (p.Val1034Met)	WWC2 (V1058M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555420	NM_024949.6(WWC2):c.3113C>T (p.Thr1038Ile)	WWC2 (T1062I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551723	NM_024949.6(WWC2):c.3118C>T (p.Arg1040Cys)	WWC2 (R1064C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610696	NM_024949.6(WWC2):c.3125G>C (p.Ser1042Thr)	WWC2 (S1042T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544995	NM_024949.6(WWC2):c.3190C>T (p.Arg1064Trp)	WWC2 (R1064W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262387	NM_024949.6(WWC2):c.3191G>A (p.Arg1064Gln)	WWC2 (R1064Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 776033	NM_024949.6(WWC2):c.3195A>G (p.Thr1065=)	WWC2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2375939	NM_024949.6(WWC2):c.3244C>T (p.Arg1082Cys)	WWC2 (R1082C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369766	NM_024949.6(WWC2):c.3245G>T (p.Arg1082Leu)	WWC2 (R1106L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 207935	NM_024949.6(WWC2):c.3260T>C (p.Leu1087Pro)	WWC2 (L1087P)	Single nucleotide variant (missense variant)	Long QT syndrome	GLikely benign
Select item 2353136	NM_024949.6(WWC2):c.3280C>G (p.Arg1094Gly)	WWC2 (R1118G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190879	NM_024949.6(WWC2):c.3457G>A (p.Val1153Met)	WWC2 (V1153M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206498	NM_024949.6(WWC2):c.3463C>T (p.Arg1155Trp)	WWC2 (R1155W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493523	NM_024949.6(WWC2):c.3493C>T (p.Arg1165Trp)	WWC2 (R1189W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1808093	GRCh37/hg19 4q35.1(chr4:183958652-184213971)x3	WWC2	Copy number gain	not provided	GUncertain significance

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Items: 63