Wnt9b Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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84 records found for search term Wnt9b

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405289796	CV3213929	single nucleotide variant	NM_003396.3(WNT9B):c.335-7G>C	WNT9B-related disorder [RCV003926782]	likely benign	17	46875094	46875094	Human		name , trait , alternate_id
597928583	CV3837311	single nucleotide variant	NM_003396.3(WNT9B):c.600+8T>G	not provided [RCV005185469]	likely benign	17	46875374	46875374	Human		name
597840216	CV3737076	single nucleotide variant	NM_003396.3(WNT9B):c.334+13G>A	not provided [RCV005064556]	likely benign	17	46872786	46872786	Human		name
597859693	CV3832901	single nucleotide variant	NM_003396.3(WNT9B):c.601-11C>T	not provided [RCV005174814]	likely benign	17	46876234	46876234	Human		name
405272835	CV3190646	single nucleotide variant	NM_001320458.2(WNT9B):c.905-5C>T	WNT9B-related disorder [RCV003907084]	benign	17	46885029	46885029	Human		name , trait , alternate_id
405276370	CV3212881	single nucleotide variant	NM_001320458.2(WNT9B):c.905-4G>A	WNT9B-related disorder [RCV003944753]	likely benign	17	46885030	46885030	Human		name , trait , alternate_id
597867430	CV3739154	single nucleotide variant	NM_003396.3(WNT9B):c.24C>T (p.Ala8=)	not provided [RCV005068221]	likely benign	17	46851662	46851662	Human		name
151733805	CV1336639	duplication	NM_003396.3(WNT9B):c.11dup (p.Pro5fs)	Renal hypoplasia [RCV001849869]	likely pathogenic	17	46851643	46851644	Human	2	name
405237685	CV2969798	single nucleotide variant	NM_003396.3(WNT9B):c.4C>A (p.Arg2Ser)	not provided [RCV003683279]	uncertain significance	17	46851642	46851642	Human		name
152110385	CV1536977	single nucleotide variant	NM_003396.3(WNT9B):c.162G>A (p.Gln54=)	WNT9B-related disorder [RCV003950972]\|not provided [RCV002215404]	likely benign	17	46872601	46872601	Human		name , trait , alternate_id
152034553	CV1610614	single nucleotide variant	NM_003396.3(WNT9B):c.144C>T (p.Gly48=)	not provided [RCV002125115]	benign\|likely benign	17	46872583	46872583	Human		name
152130203	CV1630923	single nucleotide variant	NM_003396.3(WNT9B):c.135G>A (p.Pro45=)	not provided [RCV002118986]	benign	17	46872574	46872574	Human		name
156045294	CV2093257	single nucleotide variant	NM_003396.3(WNT9B):c.234G>A (p.Leu78=)	not provided [RCV002867595]	likely benign	17	46872673	46872673	Human		name
405294468	CV3211616	single nucleotide variant	NM_003396.3(WNT9B):c.135G>C (p.Pro45=)	WNT9B-related disorder [RCV003934409]	likely benign	17	46872574	46872574	Human		name , trait , alternate_id
15168621	CV715507	single nucleotide variant	NM_003396.3(WNT9B):c.168C>T (p.Asp56=)	not provided [RCV000971651]	benign	17	46872607	46872607	Human		name
152159413	CV1544398	single nucleotide variant	NM_003396.3(WNT9B):c.846G>C (p.Val282=)	not provided [RCV002122925]	benign	17	46876490	46876490	Human		name
152137141	CV1652260	single nucleotide variant	NM_003396.3(WNT9B):c.399G>T (p.Arg133=)	not provided [RCV002083662]	benign	17	46875165	46875165	Human		name
156369040	CV1922700	single nucleotide variant	NM_003396.3(WNT9B):c.423G>A (p.Glu141=)	not provided [RCV002633227]	likely benign	17	46875189	46875189	Human		name
156150490	CV1929214	single nucleotide variant	NM_003396.3(WNT9B):c.573C>T (p.Asp191=)	not provided [RCV002623985]	benign	17	46875339	46875339	Human		name
156326558	CV2116043	single nucleotide variant	NM_003396.3(WNT9B):c.594C>T (p.Gly198=)	WNT9B-related disorder [RCV003936406]\|not provided [RCV002938116]	benign\|likely benign	17	46875360	46875360	Human		name , trait , alternate_id
401904030	CV2811448	single nucleotide variant	NM_003396.3(WNT9B):c.85G>A (p.Gly29Arg)	not provided [RCV003419762]	likely benign	17	46872524	46872524	Human		name
405191394	CV2875819	single nucleotide variant	NM_003396.3(WNT9B):c.766T>C (p.Leu256=)	not provided [RCV003550432]	likely benign	17	46876410	46876410	Human		name
405204910	CV3068034	single nucleotide variant	NM_003396.3(WNT9B):c.588C>T (p.His196=)	WNT9B-related disorder [RCV003909121]\|not provided [RCV003731209]	likely benign	17	46875354	46875354	Human		name , trait , alternate_id
405141933	CV3125878	single nucleotide variant	NM_003396.3(WNT9B):c.375C>T (p.Ala125=)	not provided [RCV003816793]	likely benign	17	46875141	46875141	Human		name
597871667	CV3849360	single nucleotide variant	NM_003396.3(WNT9B):c.480C>T (p.Gly160=)	not provided [RCV005197541]	likely benign	17	46875246	46875246	Human		name
598192351	CV3937214	single nucleotide variant	NM_003396.3(WNT9B):c.28G>A (p.Ala10Thr)	Inborn genetic diseases [RCV005288507]	uncertain significance	17	46851666	46851666	Human	1	name
598275540	CV3937215	single nucleotide variant	NM_003396.3(WNT9B):c.56C>T (p.Ala19Val)	Inborn genetic diseases [RCV005304674]	uncertain significance	17	46851694	46851694	Human	1	name
15139816	CV715508	single nucleotide variant	NM_003396.3(WNT9B):c.627G>A (p.Thr209=)	not provided [RCV000966030]	benign	17	46876271	46876271	Human		name
15103291	CV771601	single nucleotide variant	NM_003396.3(WNT9B):c.414G>A (p.Gly138=)	not provided [RCV000937168]	likely benign	17	46875180	46875180	Human		name
152060120	CV1540576	single nucleotide variant	NM_003396.3(WNT9B):c.281G>A (p.Arg94Gln)	WNT9B-related disorder [RCV003958826]\|not provided [RCV002110010]	benign	17	46872720	46872720	Human		name , trait , alternate_id
152157537	CV1630578	single nucleotide variant	NM_003396.3(WNT9B):c.140A>G (p.Gln47Arg)	not provided [RCV002122632]	benign	17	46872579	46872579	Human		name
155997561	CV2168814	single nucleotide variant	NM_003396.3(WNT9B):c.179T>G (p.Leu60Arg)	not provided [RCV003017123]	uncertain significance	17	46872618	46872618	Human		name
405166811	CV3059763	single nucleotide variant	NM_003396.3(WNT9B):c.188G>A (p.Arg63Gln)	not provided [RCV003727513]	uncertain significance	17	46872627	46872627	Human		name
405260383	CV3204042	single nucleotide variant	NM_003396.3(WNT9B):c.290G>A (p.Arg97His)	WNT9B-related disorder [RCV003943920]	likely benign	17	46872729	46872729	Human		name , trait , alternate_id
405812216	CV3352973	single nucleotide variant	NM_003396.3(WNT9B):c.214C>T (p.Pro72Ser)	Inborn genetic diseases [RCV004483173]	uncertain significance	17	46872653	46872653	Human	1	name
407455482	CV3488009	single nucleotide variant	NM_003396.3(WNT9B):c.184C>T (p.Arg62Trp)	Inborn genetic diseases [RCV004685578]	uncertain significance	17	46872623	46872623	Human	1	name
597960380	CV3843637	single nucleotide variant	NM_003396.3(WNT9B):c.290G>T (p.Arg97Leu)	not provided [RCV005192674]	uncertain significance	17	46872729	46872729	Human		name
598192345	CV3937213	single nucleotide variant	NM_003396.3(WNT9B):c.280C>T (p.Arg94Trp)	Inborn genetic diseases [RCV005288506]	uncertain significance	17	46872719	46872719	Human	1	name
598192356	CV3937216	single nucleotide variant	NM_003396.3(WNT9B):c.232C>A (p.Leu78Met)	Inborn genetic diseases [RCV005288508]	uncertain significance	17	46872671	46872671	Human	1	name
127322409	CV1158001	single nucleotide variant	NM_003396.3(WNT9B):c.773G>A (p.Arg258His)	not provided [RCV001523517]	benign	17	46876417	46876417	Human		name
151733798	CV1336638	single nucleotide variant	NM_003396.3(WNT9B):c.949G>A (p.Gly317Arg)	Cystic renal dysplasia [RCV001849868]	likely pathogenic	17	46876593	46876593	Human	2	name
151812239	CV1376834	single nucleotide variant	NM_003396.3(WNT9B):c.665G>T (p.Arg222Leu)	not provided [RCV001900068]	uncertain significance	17	46876309	46876309	Human		name
151785231	CV1434792	single nucleotide variant	NM_003396.3(WNT9B):c.665G>A (p.Arg222His)	WNT9B-related disorder [RCV004758199]\|not provided [RCV001897618]	uncertain significance	17	46876309	46876309	Human		name , trait , alternate_id
151842251	CV1438332	single nucleotide variant	NM_003396.3(WNT9B):c.389C>A (p.Thr130Asn)	not provided [RCV001921671]	uncertain significance	17	46875155	46875155	Human		name
151766397	CV1469994	single nucleotide variant	NM_003396.3(WNT9B):c.661G>A (p.Val221Met)	not provided [RCV001914549]	uncertain significance	17	46876305	46876305	Human		name
152159403	CV1544396	single nucleotide variant	NM_003396.3(WNT9B):c.317T>C (p.Met106Thr)	WNT9B-related disorder [RCV003978690]\|not provided [RCV002122924]	benign	17	46872756	46872756	Human		name , trait , alternate_id
152154200	CV1579436	single nucleotide variant	NM_003396.3(WNT9B):c.522C>A (p.Ser174Arg)	WNT9B-related disorder [RCV003933632]\|not provided [RCV002158627]	benign\|likely benign	17	46875288	46875288	Human		name , trait , alternate_id
152140620	CV1628798	single nucleotide variant	NM_003396.3(WNT9B):c.589G>A (p.Val197Met)	not provided [RCV002100722]	likely benign	17	46875355	46875355	Human		name
156332606	CV1895412	single nucleotide variant	NM_003396.3(WNT9B):c.398G>A (p.Arg133Gln)	not provided [RCV003089891]	uncertain significance	17	46875164	46875164	Human		name
156417638	CV1967083	single nucleotide variant	NM_003396.3(WNT9B):c.461G>C (p.Arg154Pro)	not provided [RCV002590292]	uncertain significance	17	46875227	46875227	Human		name
156204351	CV2110202	single nucleotide variant	NM_003396.3(WNT9B):c.731C>T (p.Ser244Leu)	WNT9B-related disorder [RCV003961251]\|not provided [RCV002957498]	benign\|likely benign	17	46876375	46876375	Human		name , trait , alternate_id
156284864	CV2114793	single nucleotide variant	NM_003396.3(WNT9B):c.701C>T (p.Thr234Met)	not provided [RCV002921911]	uncertain significance	17	46876345	46876345	Human		name
156316460	CV2137745	single nucleotide variant	NM_003396.3(WNT9B):c.454G>A (p.Glu152Lys)	not provided [RCV002962932]	uncertain significance	17	46875220	46875220	Human		name
156310490	CV2165206	single nucleotide variant	NM_003396.3(WNT9B):c.405C>G (p.Cys135Trp)	not provided [RCV003028549]	uncertain significance	17	46875171	46875171	Human		name
156176307	CV2181480	single nucleotide variant	NM_003396.3(WNT9B):c.376G>A (p.Ala126Thr)	not provided [RCV003057382]	benign	17	46875142	46875142	Human		name
156094576	CV2300309	single nucleotide variant	NM_003396.3(WNT9B):c.985T>C (p.Phe329Leu)	Inborn genetic diseases [RCV002870042]	uncertain significance	17	46876629	46876629	Human	1	name
156356803	CV2318178	single nucleotide variant	NM_003396.3(WNT9B):c.680A>T (p.Gln227Leu)	Inborn genetic diseases [RCV002940741]	uncertain significance	17	46876324	46876324	Human	1	name
401739604	CV2704591	single nucleotide variant	NM_003396.3(WNT9B):c.650G>T (p.Gly217Val)	Inborn genetic diseases [RCV003292128]	uncertain significance	17	46876294	46876294	Human	1	name
401868941	CV2767383	single nucleotide variant	NM_003396.3(WNT9B):c.808C>T (p.Leu270Phe)	Inborn genetic diseases [RCV003345575]	uncertain significance	17	46876452	46876452	Human	1	name
401867300	CV2773250	single nucleotide variant	NM_003396.3(WNT9B):c.320G>T (p.Gly107Val)	Inborn genetic diseases [RCV003360212]	uncertain significance	17	46872759	46872759	Human	1	name
401866215	CV2775461	single nucleotide variant	NM_003396.3(WNT9B):c.668C>T (p.Thr223Ile)	Inborn genetic diseases [RCV003359925]	uncertain significance	17	46876312	46876312	Human	1	name
401895006	CV2792673	single nucleotide variant	NM_003396.3(WNT9B):c.416G>A (p.Arg139His)	Inborn genetic diseases [RCV003372071]	uncertain significance	17	46875182	46875182	Human	1	name
405223583	CV2887550	single nucleotide variant	NM_003396.3(WNT9B):c.565C>T (p.Arg189Trp)	Inborn genetic diseases [RCV004369138]\|not provided [RCV003554293]	uncertain significance	17	46875331	46875331	Human	1	name
405235985	CV2887778	single nucleotide variant	NM_003396.3(WNT9B):c.974G>A (p.Arg325His)	not provided [RCV003556401]	uncertain significance	17	46876618	46876618	Human		name
405241240	CV3060952	single nucleotide variant	NM_003396.3(WNT9B):c.597C>G (p.Ile199Met)	not provided [RCV003737230]	uncertain significance	17	46875363	46875363	Human		name
402474113	CV3182694	single nucleotide variant	NM_003396.3(WNT9B):c.875G>A (p.Arg292Gln)	not provided [RCV003874937]	uncertain significance	17	46876519	46876519	Human		name
405812218	CV3352974	single nucleotide variant	NM_003396.3(WNT9B):c.811A>G (p.Thr271Ala)	Inborn genetic diseases [RCV004483174]\|not provided [RCV005104775]	likely benign\|uncertain significance	17	46876455	46876455	Human	1	name
405812220	CV3352975	single nucleotide variant	NM_003396.3(WNT9B):c.952C>T (p.Arg318Trp)	Inborn genetic diseases [RCV004483175]	uncertain significance	17	46876596	46876596	Human	1	name
407455485	CV3488010	single nucleotide variant	NM_003396.3(WNT9B):c.920G>A (p.Arg307Gln)	Inborn genetic diseases [RCV004685579]	uncertain significance	17	46876564	46876564	Human	1	name
407455487	CV3488011	single nucleotide variant	NM_003396.3(WNT9B):c.874C>T (p.Arg292Trp)	Inborn genetic diseases [RCV004685580]	uncertain significance	17	46876518	46876518	Human	1	name
407465518	CV3488012	single nucleotide variant	NM_003396.3(WNT9B):c.461G>A (p.Arg154Gln)	Inborn genetic diseases [RCV004688789]	uncertain significance	17	46875227	46875227	Human	1	name
407455491	CV3488014	single nucleotide variant	NM_003396.3(WNT9B):c.441C>G (p.Asp147Glu)	Inborn genetic diseases [RCV004685582]	uncertain significance	17	46875207	46875207	Human	1	name
407455492	CV3488015	single nucleotide variant	NM_003396.3(WNT9B):c.549C>A (p.Asn183Lys)	Inborn genetic diseases [RCV004685583]	uncertain significance	17	46875315	46875315	Human	1	name
597631096	CV3624276	single nucleotide variant	NM_003396.3(WNT9B):c.772C>T (p.Arg258Cys)	Inborn genetic diseases [RCV004967521]	uncertain significance	17	46876416	46876416	Human	1	name
597631099	CV3624277	single nucleotide variant	NM_003396.3(WNT9B):c.662T>C (p.Val221Ala)	Inborn genetic diseases [RCV004967522]	uncertain significance	17	46876306	46876306	Human	1	name
597631101	CV3624280	single nucleotide variant	NM_003396.3(WNT9B):c.824C>T (p.Ala275Val)	Inborn genetic diseases [RCV004967523]	uncertain significance	17	46876468	46876468	Human	1	name
597631104	CV3624281	single nucleotide variant	NM_003396.3(WNT9B):c.823G>A (p.Ala275Thr)	Inborn genetic diseases [RCV004967524]	uncertain significance	17	46876467	46876467	Human	1	name
597631106	CV3624282	single nucleotide variant	NM_003396.3(WNT9B):c.446C>T (p.Pro149Leu)	Inborn genetic diseases [RCV004967525]	uncertain significance	17	46875212	46875212	Human	1	name
597631107	CV3624283	single nucleotide variant	NM_003396.3(WNT9B):c.559C>T (p.Arg187Trp)	Inborn genetic diseases [RCV004967526]	uncertain significance	17	46875325	46875325	Human	1	name
597631110	CV3624284	single nucleotide variant	NM_003396.3(WNT9B):c.794C>T (p.Ala265Val)	Inborn genetic diseases [RCV004967527]	uncertain significance	17	46876438	46876438	Human	1	name
405275805	CV3208501	single nucleotide variant	NM_001320458.2(WNT9B):c.912T>C (p.Ser304=)	WNT9B-related disorder [RCV003939591]	likely benign	17	46885041	46885041	Human		name , trait , alternate_id
405273635	CV3210283	single nucleotide variant	NM_001320458.2(WNT9B):c.981G>T (p.Leu327=)	WNT9B-related disorder [RCV003914513]	benign	17	46885110	46885110	Human		name , trait , alternate_id
405274446	CV3214010	single nucleotide variant	NM_001320458.2(WNT9B):c.963G>A (p.Ala321=)	WNT9B-related disorder [RCV003926857]	likely benign	17	46885092	46885092	Human		name , trait , alternate_id
405279236	CV3199741	single nucleotide variant	NM_001320458.2(WNT9B):c.961G>A (p.Ala321Thr)	WNT9B-related disorder [RCV003973810]	benign	17	46885090	46885090	Human		name , trait , alternate_id

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