WNT2B[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 154886	GRCh38/hg38 1p21.1-12(chr1:104325484-119977655)x3	LINC01780, LINC02868 +563 more	Copy number gain	See cases	GPathogenic
Select item 58084	GRCh38/hg38 1p13.3-12(chr1:109756630-118650204)x3	ADORA3, AHCYL1 +391 more	Copy number gain	See cases	GPathogenic
Select item 57493	GRCh38/hg38 1p13.2(chr1:112147402-113470058)x3	TAFA3, WNT2B +61 more	Copy number gain	See cases	GUncertain significance
Select item 2877051	NM_024494.3(WNT2B):c.9A>G (p.Arg3=)	LOC129931208, WNT2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2119068	NM_024494.3(WNT2B):c.11C>T (p.Pro4Leu)	LOC129931208, WNT2B (P4L)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2819968	NM_024494.3(WNT2B):c.12G>A (p.Pro4=)	LOC129931208, WNT2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2776011	NM_024494.3(WNT2B):c.12G>C (p.Pro4=)	LOC129931208, WNT2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1972665	NM_024494.3(WNT2B):c.13G>C (p.Gly5Arg)	LOC129931208, WNT2B (G5R)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2100215	NM_024494.3(WNT2B):c.23A>C (p.Glu8Ala)	LOC129931208, WNT2B (E8A)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1970963	NM_024494.3(WNT2B):c.25G>A (p.Glu9Lys)	LOC129931208, WNT2B (E9K)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 1973414	NM_024494.3(WNT2B):c.35A>G (p.Gln12Arg)	LOC129931208, WNT2B (Q12R)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3333214	NM_024494.3(WNT2B):c.37C>T (p.Leu13Phe)	LOC129931208, WNT2B (L13F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2086741	NM_024494.3(WNT2B):c.47G>C (p.Arg16Pro)	LOC122094899, LOC129931208 +1 more (R16P)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1971329	NM_024494.3(WNT2B):c.49C>T (p.Arg17Cys)	LOC122094899, LOC129931208 +1 more (R17C)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1973531	NM_024494.3(WNT2B):c.52G>A (p.Ala18Thr)	LOC122094899, WNT2B (A18T)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2810135	NM_024494.3(WNT2B):c.54C>G (p.Ala18=)	LOC122094899, WNT2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1972774	NM_024494.3(WNT2B):c.62C>G (p.Pro21Arg)	LOC122094899, WNT2B (P21R)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2309266	NM_024494.3(WNT2B):c.65T>C (p.Val22Ala)	LOC122094899, WNT2B (V22A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1977262	NM_024494.3(WNT2B):c.67C>T (p.Pro23Ser)	LOC122094899, WNT2B (P23S)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2776256	NM_024494.3(WNT2B):c.69T>C (p.Pro23=)	LOC122094899, WNT2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1977921	NM_024494.3(WNT2B):c.73C>A (p.Pro25Thr)	LOC122094899, WNT2B (P25T)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1977866	NM_024494.3(WNT2B):c.78G>A (p.Ser26=)	LOC122094899, WNT2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2516583	NM_024494.3(WNT2B):c.79C>T (p.Pro27Ser)	LOC122094899, WNT2B (P27S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1970983	NM_024494.3(WNT2B):c.82G>A (p.Ala28Thr)	LOC122094899, WNT2B (A28T)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2795858	NM_024494.3(WNT2B):c.90C>T (p.Pro30=)	WNT2B, LOC122094899	Single nucleotide variant (intron variant +1 more)	not provided	GLikely benign
Select item 3190725	NM_024494.3(WNT2B):c.94G>C (p.Gly32Arg)	LOC122094899, WNT2B (G32R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2867647	NM_024494.3(WNT2B):c.102G>A (p.Arg34=)	LOC122094899, WNT2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2745879	NM_024494.3(WNT2B):c.126C>G (p.Ala42=)	LOC122094899, WNT2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2013692	NM_024494.3(WNT2B):c.139CTG[5] (p.Leu50_Thr51insLeu)	LOC122094899, WNT2B	Microsatellite (inframe_insertion +1 more)	not provided	GUncertain significance
Select item 2876619	NM_024494.3(WNT2B):c.150G>A (p.Leu50=)	LOC122094899, WNT2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2055556	NM_024494.3(WNT2B):c.151A>G (p.Thr51Ala)	LOC122094899, WNT2B (T51A)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2862160	NM_024494.3(WNT2B):c.153G>T (p.Thr51=)	LOC122094899, WNT2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2127316	NM_024494.3(WNT2B):c.158C>G (p.Pro53Arg)	LOC122094899, WNT2B (P53R)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1973984	NM_024494.3(WNT2B):c.160G>A (p.Ala54Thr)	LOC122094899, WNT2B (A54T)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2062623	NM_024494.3(WNT2B):c.176C>G (p.Ser59Cys)	LOC122094899, WNT2B (S59C)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2123833	NM_024494.3(WNT2B):c.182+8del	LOC122094899, WNT2B	Deletion (intron variant)	not provided	GLikely benign
Select item 2869382	NM_024494.3(WNT2B):c.182+15C>A	LOC122094899, WNT2B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1973657	NM_024494.3(WNT2B):c.183-13C>T	WNT2B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2003963	NM_024494.3(WNT2B):c.194C>T (p.Ala65Val)	WNT2B (A65V +1 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 2112949	NM_024494.3(WNT2B):c.199G>T (p.Gly67Trp)	WNT2B (G67W +1 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 2183279	NM_024494.3(WNT2B):c.201G>A (p.Gly67=)	WNT2B	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 545432	NM_024494.3(WNT2B):c.205C>T (p.Arg69Ter)	WNT2B (R50* +1 more)	Single nucleotide variant (nonsense +1 more)	Diarrhea 9 +5 more	GPathogenic
Select item 1973494	NM_024494.3(WNT2B):c.222T>C (p.Asn74=)	WNT2B	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 1898254	NM_024494.3(WNT2B):c.225C>T (p.Ile75=)	WNT2B	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2025024	NM_024494.3(WNT2B):c.228T>C (p.Pro76=)	WNT2B	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 1973928	NM_024494.3(WNT2B):c.242G>A (p.Arg81Gln)	WNT2B (R81Q +1 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 2132434	NM_024494.3(WNT2B):c.250C>T (p.Gln84Ter)	WNT2B (Q84* +1 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GPathogenic
Select item 2107953	NM_024494.3(WNT2B):c.252G>C (p.Gln84His)	WNT2B (Q65H +1 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 2163807	NM_024494.3(WNT2B):c.289G>A (p.Gly97Ser)	WNT2B (G78S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2958271	NM_024494.3(WNT2B):c.291C>T (p.Gly97=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 718973	NM_024494.3(WNT2B):c.302G>A (p.Arg101Gln)	WNT2B (R101Q +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 252739	NM_024494.3(WNT2B):c.313C>T (p.Arg105Ter)	WNT2B (R105* +2 more)	Single nucleotide variant (nonsense)	not specified	GUncertain significance
Select item 3190723	NM_024494.3(WNT2B):c.314G>A (p.Arg105Gln)	WNT2B (R13Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2018411	NM_024494.3(WNT2B):c.321T>C (p.Cys107=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2704878	NM_024494.3(WNT2B):c.324G>A (p.Gln108=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2178300	NM_024494.3(WNT2B):c.334C>T (p.Arg112Cys)	WNT2B (R93C +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2003996	NM_024494.3(WNT2B):c.351C>T (p.Asn117=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1975025	NM_024494.3(WNT2B):c.366C>T (p.Asp122=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2190366	NM_024494.3(WNT2B):c.368G>A (p.Arg123Gln)	WNT2B (R104Q +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2139654	NM_024494.3(WNT2B):c.377C>G (p.Thr126Ser)	WNT2B (T126S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2001821	NM_024494.3(WNT2B):c.387C>T (p.Gly129=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1977134	NM_024494.3(WNT2B):c.403+15C>T	WNT2B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2074796	NM_024494.3(WNT2B):c.404-11TC[3]	WNT2B	Microsatellite (intron variant)	not provided	GLikely benign
Select item 2033044	NM_024494.3(WNT2B):c.404-6C>A	WNT2B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 984423	NM_024494.3(WNT2B):c.423del (p.Phe141fs)	WNT2B (F122fs +2 more)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 2031611	NM_024494.3(WNT2B):c.426A>G (p.Val142=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1994649	NM_024494.3(WNT2B):c.433A>T (p.Ile145Phe)	WNT2B (I145F +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2173640	NM_024494.3(WNT2B):c.456C>T (p.His152=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2045490	NM_024494.3(WNT2B):c.457G>A (p.Ala153Thr)	WNT2B (A61T +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2741236	NM_024494.3(WNT2B):c.468C>G (p.Arg156=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2057211	NM_024494.3(WNT2B):c.468C>T (p.Arg156=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3333215	NM_024494.3(WNT2B):c.491G>T (p.Ser164Ile)	WNT2B (S72I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2850986	NM_024494.3(WNT2B):c.504T>C (p.Cys168=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1981594	NM_024494.3(WNT2B):c.518G>A (p.Arg173His)	WNT2B (R173H +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2154862	NM_024494.3(WNT2B):c.539G>A (p.Arg180His)	WNT2B (R161H +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2308739	NM_024494.3(WNT2B):c.551A>C (p.Asp184Ala)	WNT2B (D165A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2085920	NM_024494.3(WNT2B):c.582C>T (p.Tyr194=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2068511	NM_024494.3(WNT2B):c.601G>T (p.Ala201Ser)	WNT2B (A182S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2241026	NM_024494.3(WNT2B):c.602C>T (p.Ala201Val)	WNT2B (A109V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2054128	NM_024494.3(WNT2B):c.603C>T (p.Ala201=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2193275	NM_024494.3(WNT2B):c.621G>T (p.Glu207Asp)	WNT2B (E115D +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1923920	NM_024494.3(WNT2B):c.641G>A (p.Arg214Gln)	WNT2B (R122Q +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2056303	NM_024494.3(WNT2B):c.642G>A (p.Arg214=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2742722	NM_024494.3(WNT2B):c.645C>T (p.Ala215=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1980120	NM_024494.3(WNT2B):c.650T>C (p.Met217Thr)	WNT2B (M125T +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3190724	NM_024494.3(WNT2B):c.668G>A (p.Arg223His)	WNT2B (R131H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325715	NM_024494.3(WNT2B):c.692G>C (p.Arg231Pro)	WNT2B (R212P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1976111	NM_024494.3(WNT2B):c.692G>A (p.Arg231Gln)	WNT2B (R139Q +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2019807	NM_024494.3(WNT2B):c.719A>G (p.His240Arg)	WNT2B (H148R +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 984424	NM_024494.3(WNT2B):c.722G>A (p.Gly241Asp)	WNT2B (G149D +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2070181	NM_024494.3(WNT2B):c.723C>T (p.Gly241=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 780255	NM_024494.3(WNT2B):c.732T>C (p.Gly244=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2800852	NM_024494.3(WNT2B):c.745C>T (p.Arg249Cys)	WNT2B (R157C +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2113841	NM_024494.3(WNT2B):c.760G>A (p.Ala254Thr)	WNT2B (A235T +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2070210	NM_024494.3(WNT2B):c.779G>A (p.Arg260His)	WNT2B (R241H +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2796114	NM_024494.3(WNT2B):c.799C>T (p.Arg267Ter)	WNT2B (R175* +2 more)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2179278	NM_024494.3(WNT2B):c.802C>T (p.Arg268Cys)	WNT2B (R268C +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2727253	NM_024494.3(WNT2B):c.816T>A (p.Ala272=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2083761	NM_024494.3(WNT2B):c.816T>C (p.Ala272=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2728592	NM_024494.3(WNT2B):c.819G>A (p.Val273=)	WNT2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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