Wnt8a Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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37 records found for search term Wnt8a

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401883557	CV2757986	single nucleotide variant	NM_001300939.2(WNT8A):c.-5G>A	not specified [RCV004339160]	uncertain significance	5	138084123	138084123	Human		name
329373429	CV2434247	single nucleotide variant	NM_001300939.2(WNT8A):c.-32A>G	not specified [RCV004251923]	likely benign	5	138084096	138084096	Human		name
405277102	CV3198733	single nucleotide variant	NM_001300939.2(WNT8A):c.*405G>A	WNT8A-related disorder [RCV003904058]	likely benign	5	138091478	138091478	Human		name , trait , alternate_id
8631386	CV86547	single nucleotide variant	NM_058244.3(WNT8A):c.801C>T (p.Ile267=)	Malignant melanoma [RCV000066638]	not provided	5	138090818	138090818	Human		name
8625909	CV81033	single nucleotide variant	NM_058244.3(WNT8A):c.1044G>A (p.Lys348=)	Malignant melanoma [RCV000061111]	not provided	5	138091061	138091061	Human		name
151662630	CV1330566	single nucleotide variant	NM_001300939.2(WNT8A):c.142A>G (p.Ile48Val)	Hypospadias [RCV001824103]	uncertain significance	5	138084269	138084269	Human	2	name
155978890	CV2247143	single nucleotide variant	NM_001300939.2(WNT8A):c.152C>A (p.Pro51His)	not specified [RCV004114673]	uncertain significance	5	138084279	138084279	Human		name
156181596	CV2327833	single nucleotide variant	NM_001300939.2(WNT8A):c.197A>C (p.Gln66Pro)	not specified [RCV004179171]	uncertain significance	5	138084538	138084538	Human		name
155967376	CV2329910	single nucleotide variant	NM_001300939.2(WNT8A):c.239G>T (p.Arg80Leu)	not specified [RCV004183365]	uncertain significance	5	138084580	138084580	Human		name
156078174	CV2331941	single nucleotide variant	NM_001300939.2(WNT8A):c.173C>T (p.Thr58Met)	not specified [RCV004186592]	uncertain significance	5	138084514	138084514	Human		name
407524866	CV3488000	single nucleotide variant	NM_001300939.2(WNT8A):c.178A>G (p.Ser60Gly)	not specified [RCV004678587]	uncertain significance	5	138084519	138084519	Human		name
597800112	CV3624263	single nucleotide variant	NM_001300939.2(WNT8A):c.221T>G (p.Phe74Cys)	not specified [RCV004879996]	uncertain significance	5	138084562	138084562	Human		name
598275531	CV3937201	single nucleotide variant	NM_001300939.2(WNT8A):c.238C>T (p.Arg80Cys)	not specified [RCV005304665]	uncertain significance	5	138084579	138084579	Human		name
598275535	CV3937205	single nucleotide variant	NM_001300939.2(WNT8A):c.290G>A (p.Arg97Lys)	not specified [RCV005304669]	uncertain significance	5	138084631	138084631	Human		name
156177212	CV2220366	single nucleotide variant	NM_001300939.2(WNT8A):c.757T>C (p.Trp253Arg)	not specified [RCV004095778]	uncertain significance	5	138090720	138090720	Human		name
156235881	CV2245467	single nucleotide variant	NM_001300939.2(WNT8A):c.799C>A (p.Leu267Met)	not specified [RCV004109247]	uncertain significance	5	138090762	138090762	Human		name
156103646	CV2260521	single nucleotide variant	NM_001300939.2(WNT8A):c.772G>A (p.Ala258Thr)	not specified [RCV004123303]	uncertain significance	5	138090735	138090735	Human		name
156177568	CV2327201	single nucleotide variant	NM_001300939.2(WNT8A):c.872G>A (p.Arg291His)	not specified [RCV004174663]	uncertain significance	5	138090835	138090835	Human		name
156079552	CV2341262	single nucleotide variant	NM_001300939.2(WNT8A):c.592T>G (p.Cys198Gly)	not specified [RCV004186674]	uncertain significance	5	138090555	138090555	Human		name
156144033	CV2358627	single nucleotide variant	NM_001300939.2(WNT8A):c.748G>A (p.Glu250Lys)	not specified [RCV004207501]	uncertain significance	5	138090711	138090711	Human		name
156383833	CV2361700	single nucleotide variant	NM_001300939.2(WNT8A):c.536A>C (p.Asn179Thr)	not specified [RCV004223184]	uncertain significance	5	138089041	138089041	Human		name
156149115	CV2394551	single nucleotide variant	NM_001300939.2(WNT8A):c.384A>T (p.Glu128Asp)	not specified [RCV004240904]	uncertain significance	5	138087894	138087894	Human		name
156197119	CV2400701	single nucleotide variant	NM_001300939.2(WNT8A):c.886A>T (p.Asn296Tyr)	not specified [RCV004242374]	uncertain significance	5	138090849	138090849	Human		name
401738507	CV2721902	single nucleotide variant	NM_001300939.2(WNT8A):c.698C>T (p.Ala233Val)	not specified [RCV004326407]	uncertain significance	5	138090661	138090661	Human		name
401769528	CV2731370	single nucleotide variant	NM_001300939.2(WNT8A):c.929G>A (p.Arg310His)	not specified [RCV004330736]	uncertain significance	5	138090892	138090892	Human		name
405812199	CV3352964	single nucleotide variant	NM_001300939.2(WNT8A):c.766G>A (p.Ala256Thr)	not specified [RCV004483164]	likely benign	5	138090729	138090729	Human		name
405812201	CV3352965	single nucleotide variant	NM_001300939.2(WNT8A):c.963G>C (p.Glu321Asp)	not specified [RCV004483165]	uncertain significance	5	138090926	138090926	Human		name
597800118	CV3624260	single nucleotide variant	NM_001300939.2(WNT8A):c.839A>C (p.Asn280Thr)	not specified [RCV004879993]	uncertain significance	5	138090802	138090802	Human		name
597800116	CV3624261	single nucleotide variant	NM_001300939.2(WNT8A):c.754C>A (p.His252Asn)	not specified [RCV004879994]	uncertain significance	5	138090717	138090717	Human		name
597800114	CV3624262	single nucleotide variant	NM_001300939.2(WNT8A):c.430G>A (p.Gly144Ser)	not specified [RCV004879995]	uncertain significance	5	138088935	138088935	Human		name
598275530	CV3937200	single nucleotide variant	NM_001300939.2(WNT8A):c.659G>A (p.Arg220Gln)	not specified [RCV005304664]	uncertain significance	5	138090622	138090622	Human		name
598275533	CV3937203	single nucleotide variant	NM_001300939.2(WNT8A):c.658C>T (p.Arg220Trp)	not specified [RCV005304667]	uncertain significance	5	138090621	138090621	Human		name
598275534	CV3937204	single nucleotide variant	NM_001300939.2(WNT8A):c.370A>G (p.Met124Val)	not specified [RCV005304668]	uncertain significance	5	138087880	138087880	Human		name
598192324	CV3937206	single nucleotide variant	NM_001300939.2(WNT8A):c.446G>T (p.Gly149Val)	not specified [RCV005288503]	uncertain significance	5	138088951	138088951	Human		name
401767195	CV2681514	single nucleotide variant	NM_001300939.2(WNT8A):c.1052A>G (p.Lys351Arg)	not specified [RCV004292046]	uncertain significance	5	138091015	138091015	Human		name
405812197	CV3352963	single nucleotide variant	NM_001300939.2(WNT8A):c.1081G>A (p.Ala361Thr)	not specified [RCV004483163]	uncertain significance	5	138091044	138091044	Human		name
598275532	CV3937202	single nucleotide variant	NM_001300939.2(WNT8A):c.1070C>G (p.Ser357Cys)	not specified [RCV005304666]	uncertain significance	5	138091033	138091033	Human		name

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