ClinVar for Gene (Select 7474) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3190733	NM_003392.7(WNT5A):c.44G>A (p.Gly15Glu)	WNT5A (G15E)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3062680	GRCh37/hg19 3p21.2-14.2(chr3:51149374-59265315)x1	ABHD14A, ABHD14B +86 more	Copy number loss	not specified	GPathogenic
Select item 3061040	NM_003392.7(WNT5A):c.625G>A (p.Gly209Ser)	WNT5A (G194S +1 more)	Single nucleotide variant (missense variant)	WNT5A-related condition	GUncertain significance
Select item 3052450	NM_003392.7(WNT5A):c.1055C>T (p.Thr352Met)	WNT5A (T337M +1 more)	Single nucleotide variant (missense variant)	WNT5A-related condition	GUncertain significance
Select item 3051031	NM_003392.7(WNT5A):c.-7C>T	WNT5A	Single nucleotide variant (5 prime UTR variant)	WNT5A-related condition	GLikely benign
Select item 3032407	NM_003392.7(WNT5A):c.7-5T>G	WNT5A	Single nucleotide variant (intron variant)	WNT5A-related condition	GLikely benign
Select item 3016484	NM_003392.7(WNT5A):c.279C>T (p.Ile93=)	WNT5A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3016161	NM_003392.7(WNT5A):c.141-13C>T	WNT5A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3004771	NM_003392.7(WNT5A):c.459G>A (p.Ala153=)	WNT5A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3004607	NM_003392.7(WNT5A):c.326G>A (p.Arg109Gln)	WNT5A (R109Q +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2988673	NM_003392.7(WNT5A):c.983C>T (p.Thr328Met)	WNT5A (T328M +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2976184	NM_003392.7(WNT5A):c.932G>T (p.Arg311Leu)	WNT5A (R311L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2972239	NM_003392.7(WNT5A):c.525G>T (p.Arg175=)	WNT5A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2968753	NM_003392.7(WNT5A):c.81A>G (p.Leu27=)	WNT5A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2958499	NM_003392.7(WNT5A):c.1128G>A (p.Gln376=)	WNT5A	Single nucleotide variant (synonymous variant)	WNT5A-related condition +1 more	GLikely benign
Select item 2914603	NM_003392.7(WNT5A):c.141-5T>C	WNT5A	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 2909421	NM_003392.7(WNT5A):c.1080C>T (p.His360=)	WNT5A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2878462	NM_003392.7(WNT5A):c.322T>C (p.Phe108Leu)	WNT5A (F108L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2872635	NM_003392.7(WNT5A):c.723T>C (p.His241=)	WNT5A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2871421	NM_003392.7(WNT5A):c.62T>C (p.Met21Thr)	WNT5A (M21T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2863568	NM_003392.7(WNT5A):c.685-13C>T	WNT5A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2856398	NM_003392.7(WNT5A):c.454C>G (p.Arg152Gly)	WNT5A (R152G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2848702	NM_003392.7(WNT5A):c.423G>A (p.Val141=)	WNT5A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2835456	NM_003392.7(WNT5A):c.145C>T (p.Leu49=)	WNT5A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2809966	NM_003392.7(WNT5A):c.41T>G (p.Leu14Trp)	WNT5A (L14W)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 2795376	NM_003392.7(WNT5A):c.317A>G (p.Tyr106Cys)	WNT5A (Y91C +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2783304	NM_003392.7(WNT5A):c.618C>T (p.His206=)	WNT5A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2775427	NM_003392.7(WNT5A):c.654G>C (p.Met218Ile)	WNT5A (M218I +1 more)	Single nucleotide variant (missense variant)	Short stature	GUncertain significance
Select item 2754685	NM_003392.7(WNT5A):c.916C>G (p.Pro306Ala)	WNT5A (P291A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2733908	NM_003392.7(WNT5A):c.568T>C (p.Tyr190His)	WNT5A (Y175H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2716562	NM_003392.7(WNT5A):c.273G>A (p.Gln91=)	WNT5A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2711706	NM_003392.7(WNT5A):c.686C>T (p.Thr229Met)	WNT5A (T229M +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2708828	NM_003392.7(WNT5A):c.121A>G (p.Ile41Val)	WNT5A (I26V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2700815	NM_003392.7(WNT5A):c.635A>G (p.Glu212Gly)	WNT5A (E197G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2700457	NM_003392.7(WNT5A):c.1116G>A (p.Glu372=)	WNT5A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2696188	NM_003392.7(WNT5A):c.260A>G (p.Gln87Arg)	WNT5A (Q72R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2695628	NM_003392.7(WNT5A):c.860_861delinsAA (p.Val287Glu)	WNT5A (V287E +1 more)	Indel (missense variant)	not provided	GUncertain significance
Select item 2633451	NM_003392.7(WNT5A):c.811G>C (p.Asp271His)	WNT5A (D256H +1 more)	Single nucleotide variant (missense variant)	WNT5A-related condition	GUncertain significance
Select item 2631957	NM_003392.7(WNT5A):c.817G>A (p.Ala273Thr)	WNT5A (A258T +1 more)	Single nucleotide variant (missense variant)	WNT5A-related condition	GUncertain significance
Select item 2616212	NM_003392.7(WNT5A):c.691T>C (p.Tyr231His)	WNT5A (Y231H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2584652	NM_003392.7(WNT5A):c.157A>T (p.Asn53Tyr)	WNT5A (N38Y +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant Robinow syndrome 1	GUncertain significance
Select item 2476745	NM_003392.7(WNT5A):c.804G>C (p.Glu268Asp)	WNT5A (E253D +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2470886	NM_003392.7(WNT5A):c.296C>T (p.Thr99Ile)	WNT5A (T84I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2444765	NM_003392.7(WNT5A):c.419_420insTC (p.Val141fs)	WNT5A (V126fs +1 more)	Insertion (frameshift variant)	not provided	GUncertain significance
Select item 2443688	NM_003392.7(WNT5A):c.588_589dup (p.Val197fs)	WNT5A (V182fs +1 more)	Duplication (frameshift variant)	not provided	GUncertain significance
Select item 2438613	NM_003392.7(WNT5A):c.890A>G (p.Gln297Arg)	WNT5A (Q282R +1 more)	Single nucleotide variant (missense variant)	Autosomal dominant Robinow syndrome 1	GUncertain significance
Select item 2424678	NC_000003.11:g.(?_55504120)_(55521013_?)del	WNT5A	Deletion	not provided	GUncertain significance
Select item 2416547	NM_003392.7(WNT5A):c.391+4G>A	WNT5A	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2379610	NM_003392.7(WNT5A):c.122T>C (p.Ile41Thr)	WNT5A (I41T +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2334962	NM_003392.7(WNT5A):c.46A>G (p.Met16Val)	WNT5A (M1V +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2317420	NM_003392.7(WNT5A):c.113A>G (p.Gln38Arg)	WNT5A (Q23R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2302202	NM_003392.7(WNT5A):c.384G>A (p.Met128Ile)	WNT5A (M113I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2292315	NM_003392.7(WNT5A):c.823G>A (p.Ala275Thr)	WNT5A (A260T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2273836	NM_003392.7(WNT5A):c.826A>T (p.Met276Leu)	WNT5A (M261L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2265386	NM_003392.7(WNT5A):c.578C>T (p.Ala193Val)	WNT5A (A178V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2264134	NM_003392.7(WNT5A):c.284A>G (p.Glu95Gly)	WNT5A (E95G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2190414	NM_003392.7(WNT5A):c.968G>A (p.Arg323His)	WNT5A (R323H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2187177	NM_003392.7(WNT5A):c.619G>T (p.Ala207Ser)	WNT5A (A192S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2183922	NM_003392.7(WNT5A):c.88T>C (p.Leu30=)	WNT5A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2183724	NM_003392.7(WNT5A):c.1062C>T (p.Arg354=)	WNT5A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2160649	NM_003392.7(WNT5A):c.141-9C>A	WNT5A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2129422	NM_003392.7(WNT5A):c.879G>T (p.Ser293=)	WNT5A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2119256	NM_003392.7(WNT5A):c.543C>T (p.Gly181=)	WNT5A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2108861	NM_003392.7(WNT5A):c.684+10G>A	WNT5A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2104367	NM_003392.7(WNT5A):c.824C>T (p.Ala275Val)	WNT5A (A260V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2103322	NM_003392.7(WNT5A):c.684+16C>T	WNT5A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2099679	NM_003392.7(WNT5A):c.563A>G (p.Tyr188Cys)	WNT5A (Y173C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2086195	NM_003392.7(WNT5A):c.504G>A (p.Ala168=)	WNT5A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2084460	NM_003392.7(WNT5A):c.818C>T (p.Ala273Val)	WNT5A (A273V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2002081	NM_003392.7(WNT5A):c.329A>T (p.His110Leu)	WNT5A (H95L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2000581	NM_003392.7(WNT5A):c.445G>A (p.Ala149Thr)	WNT5A (A134T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1990967	NM_003392.7(WNT5A):c.99T>C (p.Phe33=)	WNT5A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1990952	NM_003392.7(WNT5A):c.398G>A (p.Arg133His)	WNT5A (R118H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1985195	NM_003392.7(WNT5A):c.915C>T (p.Ser305=)	WNT5A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1984959	NM_003392.7(WNT5A):c.606G>A (p.Arg202=)	WNT5A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1979234	NM_003392.7(WNT5A):c.816C>T (p.Ser272=)	WNT5A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1978800	NM_003392.7(WNT5A):c.669C>T (p.Asn223=)	WNT5A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1972295	NM_003392.7(WNT5A):c.132T>A (p.Asn44Lys)	WNT5A (N29K +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1961906	NM_003392.7(WNT5A):c.595G>C (p.Ala199Pro)	WNT5A (A199P +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1958715	NM_003392.7(WNT5A):c.962A>G (p.Gln321Arg)	WNT5A (Q306R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1953968	NM_003392.7(WNT5A):c.164T>G (p.Val55Gly)	WNT5A (V55G +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1928672	NM_003392.7(WNT5A):c.695A>G (p.Asn232Ser)	WNT5A (N217S +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1926203	NM_003392.7(WNT5A):c.675C>A (p.Ala225=)	WNT5A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1918246	NM_003392.7(WNT5A):c.692A>G (p.Tyr231Cys)	WNT5A (Y216C +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1911005	NM_003392.7(WNT5A):c.1113G>A (p.Thr371=)	WNT5A	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1906076	NM_003392.7(WNT5A):c.878C>T (p.Ser293Leu)	WNT5A (S293L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1903305	NM_003392.7(WNT5A):c.392-6C>T	WNT5A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1897230	NM_003392.7(WNT5A):c.57T>C (p.Ser19=)	WNT5A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1897080	NM_003392.7(WNT5A):c.507C>A (p.Arg169=)	WNT5A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1803402	NM_003392.7(WNT5A):c.551A>G (p.Asp184Gly)	WNT5A (D169G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1718671	NM_003392.7(WNT5A):c.319C>A (p.Gln107Lys)	WNT5A (Q107K +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1718186	NM_003392.7(WNT5A):c.661C>T (p.His221Tyr)	WNT5A (H206Y +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1717127	NM_003392.7(WNT5A):c.80T>A (p.Leu27Gln)	WNT5A (L12Q +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1714707	NM_003392.7(WNT5A):c.1063T>C (p.Cys355Arg)	WNT5A (C340R +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1712780	NM_003392.7(WNT5A):c.*2011G>A	WNT5A	Single nucleotide variant (3 prime UTR variant)	not provided	GLikely benign
Select item 1707897	NM_003392.7(WNT5A):c.408dup (p.Phe137fs)	WNT5A (F122fs +1 more)	Duplication (frameshift variant)	not provided	GUncertain significance
Select item 1698612	NM_003392.7(WNT5A):c.289G>A (p.Ala97Thr)	WNT5A (A82T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1691703	NM_003392.7(WNT5A):c.41del (p.Leu14fs)	WNT5A (L14fs)	Deletion (5 prime UTR variant +1 more)	Autosomal dominant Robinow syndrome 1	GUncertain significance
Select item 1686384	NM_003392.7(WNT5A):c.332G>A (p.Arg111Gln)	WNT5A (R111Q +1 more)	Single nucleotide variant (missense variant)	not specified	GBenign
Select item 1659405	NM_003392.7(WNT5A):c.1032C>T (p.Tyr344=)	WNT5A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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