Uhrf2 Variant Search Result - Rat Genome Database

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43 records found for search term Uhrf2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401924354	CV2828754	single nucleotide variant	NM_152896.3(UHRF2):c.255A>G (p.Thr85=)	not provided [RCV003435708]	likely benign	9	6421013	6421013	Human		name
597789957	CV3632576	single nucleotide variant	NM_152896.3(UHRF2):c.23T>C (p.Ile8Thr)	not specified [RCV004876225]	uncertain significance	9	6413513	6413513	Human		name
405805291	CV3348154	single nucleotide variant	NM_152896.3(UHRF2):c.50A>G (p.Glu17Gly)	not specified [RCV004479675]	uncertain significance	9	6413540	6413540	Human		name
329401901	CV2457487	single nucleotide variant	NM_152896.3(UHRF2):c.112G>T (p.Val38Leu)	not specified [RCV004267303]	uncertain significance	9	6413602	6413602	Human		name
405805289	CV3348149	single nucleotide variant	NM_152896.3(UHRF2):c.278C>G (p.Ser93Cys)	not specified [RCV004479670]	uncertain significance	9	6421036	6421036	Human		name
156266212	CV2198726	single nucleotide variant	NM_152896.3(UHRF2):c.559A>C (p.Asn187His)	not specified [RCV004075733]	uncertain significance	9	6434088	6434088	Human		name
156274543	CV2202633	single nucleotide variant	NM_152896.3(UHRF2):c.346C>T (p.Arg116Cys)	not specified [RCV004082889]	uncertain significance	9	6421104	6421104	Human		name
156043788	CV2268474	single nucleotide variant	NM_152896.3(UHRF2):c.460G>T (p.Ala154Ser)	not specified [RCV004130167]	uncertain significance	9	6433989	6433989	Human		name
156265610	CV2275412	single nucleotide variant	NM_152896.3(UHRF2):c.314T>C (p.Val105Ala)	not specified [RCV004135290]	uncertain significance	9	6421072	6421072	Human		name
155998616	CV2393443	single nucleotide variant	NM_152896.3(UHRF2):c.377T>C (p.Ile126Thr)	not specified [RCV004228938]	uncertain significance	9	6421135	6421135	Human		name
156162733	CV2395729	single nucleotide variant	NM_152896.3(UHRF2):c.977G>A (p.Arg326Gln)	not specified [RCV004235263]	uncertain significance	9	6477625	6477625	Human		name
401747181	CV2698805	single nucleotide variant	NM_152896.3(UHRF2):c.786C>G (p.Phe262Leu)	not specified [RCV004301250]	uncertain significance	9	6460714	6460714	Human		name
401871606	CV2783553	single nucleotide variant	NM_152896.3(UHRF2):c.619G>A (p.Val207Ile)	not specified [RCV004365882]	uncertain significance	9	6434148	6434148	Human		name
405805285	CV3348151	single nucleotide variant	NM_152896.3(UHRF2):c.338C>T (p.Thr113Ile)	not specified [RCV004479672]	uncertain significance	9	6421096	6421096	Human		name
405805287	CV3348152	single nucleotide variant	NM_152896.3(UHRF2):c.359T>C (p.Ile120Thr)	not specified [RCV004479673]	uncertain significance	9	6421117	6421117	Human		name
405805409	CV3348153	single nucleotide variant	NM_152896.3(UHRF2):c.509C>A (p.Ser170Tyr)	not specified [RCV004479674]	uncertain significance	9	6434038	6434038	Human		name
405805293	CV3348155	single nucleotide variant	NM_152896.3(UHRF2):c.551A>G (p.Glu184Gly)	not specified [RCV004479676]	uncertain significance	9	6434080	6434080	Human		name
405805295	CV3348156	single nucleotide variant	NM_152896.3(UHRF2):c.844C>T (p.Arg282Cys)	not specified [RCV004479677]	uncertain significance	9	6460772	6460772	Human		name
407523379	CV3489180	single nucleotide variant	NM_152896.3(UHRF2):c.676G>A (p.Val226Ile)	not specified [RCV004678067]	uncertain significance	9	6460604	6460604	Human		name
407462449	CV3489181	single nucleotide variant	NM_152896.3(UHRF2):c.311G>A (p.Arg104Lys)	not specified [RCV004687966]	uncertain significance	9	6421069	6421069	Human		name
407523382	CV3489182	single nucleotide variant	NM_152896.3(UHRF2):c.308C>G (p.Pro103Arg)	not specified [RCV004678068]	uncertain significance	9	6421066	6421066	Human		name
407523385	CV3489184	single nucleotide variant	NM_152896.3(UHRF2):c.623T>C (p.Ile208Thr)	not specified [RCV004678069]	uncertain significance	9	6434152	6434152	Human		name
597789951	CV3632572	single nucleotide variant	NM_152896.3(UHRF2):c.988G>C (p.Glu330Gln)	not specified [RCV004876223]	uncertain significance	9	6477636	6477636	Human		name
597720275	CV3632573	single nucleotide variant	NM_152896.3(UHRF2):c.742G>A (p.Val248Ile)	not specified [RCV004887810]	uncertain significance	9	6460670	6460670	Human		name
597789963	CV3632577	single nucleotide variant	NM_152896.3(UHRF2):c.472C>G (p.Gln158Glu)	not specified [RCV004876226]	uncertain significance	9	6434001	6434001	Human		name
598190741	CV3925440	single nucleotide variant	NM_152896.3(UHRF2):c.449G>A (p.Ser150Asn)	not specified [RCV005288251]	uncertain significance	9	6433978	6433978	Human		name
598266379	CV3925441	single nucleotide variant	NM_152896.3(UHRF2):c.902C>T (p.Ser301Phe)	not specified [RCV005301926]	likely benign	9	6475429	6475429	Human		name
156377912	CV2207587	single nucleotide variant	NM_152896.3(UHRF2):c.2029G>T (p.Val677Leu)	not specified [RCV004090374]	uncertain significance	9	6500575	6500575	Human		name
156343037	CV2222608	single nucleotide variant	NM_152896.3(UHRF2):c.1102G>T (p.Ala368Ser)	not specified [RCV004099435]	uncertain significance	9	6477750	6477750	Human		name
156339815	CV2268013	single nucleotide variant	NM_152896.3(UHRF2):c.2140C>G (p.Leu714Val)	not specified [RCV004136569]	uncertain significance	9	6500686	6500686	Human		name
156154958	CV2314254	single nucleotide variant	NM_152896.3(UHRF2):c.2357T>A (p.Ile786Asn)	not specified [RCV004166616]	uncertain significance	9	6506127	6506127	Human		name
401749270	CV2694604	single nucleotide variant	NM_152896.3(UHRF2):c.2246T>G (p.Phe749Cys)	not specified [RCV004298722]	uncertain significance	9	6504675	6504675	Human		name
401762728	CV2720049	single nucleotide variant	NM_152896.3(UHRF2):c.1976G>C (p.Ser659Thr)	not specified [RCV004323623]	uncertain significance	9	6499902	6499902	Human		name
401862644	CV2768510	single nucleotide variant	NM_152896.3(UHRF2):c.2179T>A (p.Leu727Met)	not specified [RCV004344392]	uncertain significance	9	6504608	6504608	Human		name
401885023	CV2771149	single nucleotide variant	NM_152896.3(UHRF2):c.1106A>T (p.Tyr369Phe)	not specified [RCV004346146]	uncertain significance	9	6477754	6477754	Human		name
405805361	CV3348147	single nucleotide variant	NM_152896.3(UHRF2):c.1268G>A (p.Arg423Gln)	not specified [RCV004479668]	uncertain significance	9	6481750	6481750	Human		name
405805359	CV3348148	single nucleotide variant	NM_152896.3(UHRF2):c.2048C>T (p.Ser683Leu)	not specified [RCV004479669]	uncertain significance	9	6500594	6500594	Human		name
407462454	CV3489183	single nucleotide variant	NM_152896.3(UHRF2):c.2046T>G (p.Asp682Glu)	not specified [RCV004687967]	uncertain significance	9	6500592	6500592	Human		name
597720265	CV3632571	single nucleotide variant	NM_152896.3(UHRF2):c.2042C>T (p.Ser681Leu)	not specified [RCV004887809]	uncertain significance	9	6500588	6500588	Human		name
597720285	CV3632574	single nucleotide variant	NM_152896.3(UHRF2):c.2230G>T (p.Val744Leu)	not specified [RCV004887811]	uncertain significance	9	6504659	6504659	Human		name
597789955	CV3632575	single nucleotide variant	NM_152896.3(UHRF2):c.2057C>G (p.Ala686Gly)	not specified [RCV004876224]	uncertain significance	9	6500603	6500603	Human		name
598266374	CV3925439	single nucleotide variant	NM_152896.3(UHRF2):c.2315G>A (p.Arg772Gln)	not specified [RCV005301925]	uncertain significance	9	6506085	6506085	Human		name
598266384	CV3925442	single nucleotide variant	NM_152896.3(UHRF2):c.1949C>G (p.Pro650Arg)	not specified [RCV005301927]	uncertain significance	9	6499875	6499875	Human		name

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