iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs6160175	snp	G/T	0.375	0.216506	intron-variant	Hectd2	Mm_Celera	19:36604731	TATAGGACATATTCG[G/T]ATTCACACAAACATT	226098
rs6160835	snp	C/T	0.5	0	intron-variant	Hectd2	Mm_Celera	19:36604873	TGAAAGAGAAAGGGC[C/T]GTAAAAAGTTATTTT	226098
rs6161400	snp	C/T	0.5	0	intron-variant	Hectd2	Mm_Celera	19:36604946	TCTTAGGGGCAATAC[C/T]CTTTGTCAAGGCATC	226098
rs6251584	snp	A/G	0.5	0	intron-variant	Hectd2	Mm_Celera	19:36583274	ATAGCCAAGGACAGA[A/G]CTGTACTTGGTTCTG	226098
rs6251644	snp	A/C	0.244898	0.249948	intron-variant	Hectd2	Mm_Celera	19:36583319	ACATGTTCAAGTAAA[A/C]ATTAGCAGCANAAAG	226098
rs6264283	snp	A/C	0.5	0	intron-variant	Hectd2	Mm_Celera	19:36583330	TAAANATTAGCAGCA[A/C]AAAGGNTCAATTACA	226098
rs6264286	snp	A/G	0.5	0	intron-variant	Hectd2	Mm_Celera	19:36583336	TTAGCAGCANAAAGG[A/G]TCAATTACAAATTTT	226098
rs6264830	snp	A/G	0.375	0.216506	intron-variant	Hectd2	Mm_Celera	19:36583478	TGGGAGAATAAATGT[A/G]GGCCAGTACAAAACT	226098
rs6265859	snp	A/G	0.5	0	intron-variant	Hectd2	Mm_Celera	19:36583655	AAGAGAAGGAGAGAA[A/G]GAACTATANATTTCA	226098
rs6265873	snp	C/G	0.5	0	intron-variant	Hectd2	Mm_Celera	19:36583664	AGAGAANGAACTATA[C/G]ATTTCATCTATGAAG	226098
rs6265917	snp	C/G	0.5	0	intron-variant	Hectd2	Mm_Celera	19:36583692	AAGGGCTTTGGGGAG[C/G]ANTGGAGATGAATGG	226098
rs6265918	snp	A/G	0.5	0	intron-variant	Hectd2	Mm_Celera	19:36583694	GGGCTTTGGGGAGNA[A/G]TGGAGATGAATGGTG	226098
rs6266384	snp	G/T	0.5	0	intron-variant	Hectd2	Mm_Celera	19:36583727	CAGCTCTAACTTTAT[G/T]CAAGGTATAGTCAAA	226098
rs6266481	snp	C/G	0.5	0	intron-variant	Hectd2	Mm_Celera	19:36583778	TTTATGGAAAGCACC[C/G]TNTAAGAGCTGTTAG	226098
rs6266488	snp	C/G	0.231111	0.249285	intron-variant	Hectd2	Mm_Celera	19:36583780	TATGGAAAGCACCNT[C/G]TAAGAGCTGTTAGGA	226098
rs13483609	snp	C/T	0.286243	0.247359	intron-variant	Hectd2	Mm_Celera	19:36587224	GTCTCAGGAGTGAAT[C/T]GGATACTGCTCTTAG	226098
rs30306671	snp	G/T	0.375	0.216506	intron-variant	Hectd2	Mm_Celera	19:36569726	CTCTAGCCAAACAAC[G/T]TATGTGATGAATTAG	226098
rs30317441	snp	C/T	0.444444	0.157135	upstream-variant-2KB	Hectd2, LOC105246565	GRCm38.p3	19:36553955	AGAGGGAACGAAGGA[C/T]GGCGGGGGGCGGGGA	226098
rs30318050	snp	A/G	0.46875	0.121031	intron-variant	Hectd2	GRCm38.p3	19:36584549	TGAGAAAGGAAGGGC[A/G]CGTGTCAGGGTGAGG	226098
rs30320425	snp	C/T	0.444444	0.157135	intron-variant	Hectd2	GRCm38.p3	19:36617244	TCTTCCTCTGGTTTC[C/T]ATGTGTACACATAAG	226098
rs30321076	snp	A/G	0.49827	0.0293608	intron-variant	Hectd2	GRCm38.p3	19:36607124	AGAGTAAAAAGATGA[A/G]CAAGAACTGAAGCTG	226098
rs30329627	snp	A/G	0.444444	0.157135	intron-variant	Hectd2	Mm_Celera	19:36586134	AATGTGATTAGTTAT[A/G]TTCATGTATTTCCAA	226098
rs30348952	snp	C/T	0.375	0.216506	intron-variant	Hectd2	Mm_Celera	19:36615856	TCAAACTCAGAGATC[C/T]GCCTCCCTCTCTATC	226098
rs30349672	snp	C/T	0.444444	0.157135	intron-variant	Hectd2	GRCm38.p3	19:36566716	ACTTAGCTAGACTGG[C/T]CAATTACCTGGGTGT	226098
rs30352296	snp	A/G	0.415225	0.187619	intron-variant	Hectd2	Mm_Celera	19:36583129	CCTTCTTATCCCAGG[A/G]CACCCCATACTGAGT	226098
rs30364005	snp	G/T	0.444444	0.157135	intron-variant	Hectd2	Mm_Celera	19:36593648	ATAGGCATCTCATCC[G/T]TTAGGTTAGGAAATT	226098
rs30365661	snp	A/G	0.387812	0.208586	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	Hectd2, 1500017E21Rik	Mm_Celera	19:36619147	TAGTTTGTCACAGGT[A/G]TCCACTGGGAAAGAC	226098
rs30369314	snp	G/T	0.444444	0.157135	upstream-variant-2KB	Hectd2	GRCm38.p3	19:36552349	CCCTTTAGGTCTTTT[G/T]CCTTCCTAAATCAGA	226098
rs30370075	snp	C/T	0.375	0.216506	intron-variant	Hectd2	Mm_Celera	19:36593357	CTCCATCTGTAGTGA[C/T]TGAGAGTCTTGCTGG	226098
rs30374040	snp	A/G	0.484429	0.0868505	intron-variant	Hectd2	GRCm38.p3	19:36582954	GAAGCTGTTTGGTGA[A/G]CCGTGGAATAAGAGA	226098
rs30377274	snp	G/T	0.375	0.216506	intron-variant	Hectd2	GRCm38.p3	19:36590834	ATATGCCCAAGAGTG[G/T]TAGAGCTGGATTGTA	226098
rs30405308	snp	A/G	0.401235	0.199068	intron-variant	Hectd2	GRCm38.p3	19:36559550	AGCACACCCACTGGA[A/G]TGTTGACCACAGGAT	226098
rs30407513	snp	C/T	0.49827	0.0293608	intron-variant	Hectd2	Mm_Celera	19:36617375	TTTCTACATGAGTCA[C/T]AATTAAAAGAATGAG	226098
rs30408432	snp	C/T	0.5	0	intron-variant	Hectd2	Mm_Celera	19:36603736	TTATTGATAATATTT[C/T]TATAAATATCTTGTG	226098
rs30415801	snp	A/G	0.429688	0.173817	intron-variant, upstream-variant-2KB	Hectd2, LOC105246565	GRCm38.p3	19:36555888	TGGAAATTGTTAAAG[A/G]CAACTCTTTTATCAT	226098
rs30416578	snp	C/G	0.456747	0.140554	intron-variant	Hectd2	GRCm38.p3	19:36602830	ATGATTGGTGACTCT[C/G]TGACACAGCTTATGC	226098
rs30429814	snp	C/T	0.375	0.216506	upstream-variant-2KB, nc-transcript-variant	Hectd2, LOC105246565	GRCm38.p3	19:36553072	AAAATGAAAGGTTGG[C/T]TTTACAATGTTTGTT	226098
rs30441248	snp	A/G	0.415225	0.187619	intron-variant	Hectd2	Mm_Celera	19:36601778	TGAGGAGCTTGTTGG[A/G]ACTTCATTGTGTAAC	226098
rs30499671	snp	A/G	0.375	0.216506	intron-variant	Hectd2	Mm_Celera	19:36592368	GTTGTTTAGTTTTCA[A/G]TGATTTTGTAAGCTT	226098
rs30510758	snp	C/T	0.375	0.216506	intron-variant	Hectd2	GRCm38.p3	19:36617819	TAGCAAATGCACCGG[C/T]TTTAGGGTCAGACCT	226098
rs30554029	snp	A/G	0.375	0.216506	intron-variant	Hectd2	GRCm38.p3	19:36617739	ACTGTCATCCCCTCT[A/G]TAAGGCACACTGTTG	226098
rs30606628	snp	G/T	0.444444	0.157135	intron-variant	Hectd2	Mm_Celera	19:36612744	CCTTTCTACTATATA[G/T]AGAGAGAGAGAGAAA	226098
rs30619016	snp	A/G	0.375	0.216506	intron-variant	Hectd2	Mm_Celera	19:36609193	TTAGATCTAAAAGGA[A/G]ACTGGTGCATAATTC	226098
rs30657771	snp	C/T	0.32	0.24	intron-variant	Hectd2	GRCm38.p3	19:36576911	TGACCTCAAGCTGTA[C/T]TACAGAGCAATGGTG	226098
rs30670562	snp	A/G	0.444444	0.157135	intron-variant	Hectd2	Mm_Celera	19:36584747	CCTACACATTTATAT[A/G]CTGTTTGTATCAACT	226098
rs30696908	snp	C/T	0.48	0.0979796	intron-variant	Hectd2	Mm_Celera	19:36598521	CTCCCTCATGCATGC[C/T]GAGGCCTCGGGGGTT	226098
rs30710321	snp	C/T	0.444444	0.157135	intron-variant	Hectd2	Mm_Celera	19:36557305	CAGAAAATTAGTGTG[C/T]CATGGTTATGACGGT	226098
rs30766662	snp	A/T	0.444444	0.157135	intron-variant	Hectd2	Mm_Celera	19:36595869	ATAAATAAATCTTTT[A/T]AAAAAAAAAGAAAAG	226098
rs30805300	snp	C/T	0.375	0.216506	intron-variant	Hectd2	GRCm38.p3	19:36558415	GTGAGTGTGCATGTA[C/T]GTGTGTGTACATGTG	226098
rs30842320	snp	A/C	0.444444	0.157135	intron-variant	Hectd2	GRCm38.p3	19:36592718	GGGTAAGTAGTGTTT[A/C]TTTTACAAAGGTGGG	226098
rs30850383	snp	A/G	0.408163	0.193609	intron-variant	Hectd2	GRCm38.p3	19:36617730	GAACTAAGAACTGTC[A/G]TCCCCTCTATAAGGC	226098
rs30851162	snp	A/C	0.32	0.24	intron-variant	Hectd2	Mm_Celera	19:36610667	ACCACCCTGCCAGAT[A/C]TGAGGCTCTGGTCCC	226098
rs30910268	snp	A/G	0.5	0	intron-variant	Hectd2	GRCm38.p3	19:36600751	TTGTGATGGGAGTCT[A/G]ACCTCTCAGTGTTAC	226098
rs30915485	snp	A/G	0.493827	0.0552116	intron-variant	Hectd2	Mm_Celera	19:36606201	ATCTTGTACATCCTT[A/G]TAAAAAGTCAGATAT	226098
rs30917111	snp	A/T	0.415225	0.187619	intron-variant	Hectd2	GRCm38.p3	19:36616902	CAGAGAGGGTAGGCC[A/T]TATGCATCTTATACT	226098
rs30947361	snp	A/G	0.489796	0.070696	intron-variant	Hectd2	GRCm38.p3	19:36597775	TAATTCCTATTACTG[A/G]TAGTAGAATTCAAAT	226098
rs30989214	snp	G/T	0.444444	0.157135	intron-variant	Hectd2	Mm_Celera	19:36612746	TTTCTACTATATAGA[G/T]AGAGAGAGAGAAATG	226098
rs30991176	snp	A/G	0.444444	0.157135	intron-variant	Hectd2	Mm_Celera	19:36614633	CCTGCTCTCCTACTC[A/G]CCCACTCCCACTTCT	226098
rs30992107	snp	C/T	0.49827	0.0293608	intron-variant	Hectd2	GRCm38.p3	19:36600822	GTAGTGTGTGGTTTT[C/T]ATACATAGTGTACGA	226098
rs31008504	snp	A/G	0.375	0.216506	intron-variant	Hectd2	Mm_Celera	19:36562588	GCTAGCATGCACAAA[A/G]TGATGTTCCATCCCC	226098
rs31009339	snp	A/T	0.375	0.216506	intron-variant	Hectd2	Mm_Celera	19:36593370	GACTGAGAGTCTTGC[A/T]GGGTATAGTAGTGTG	226098
rs31039933	snp	A/G	0.387812	0.208586	intron-variant	Hectd2	Mm_Celera	19:36612018	TGACACCTCTTCTTA[A/G]TATAATTGTCACTGG	226098
rs31042743	snp	A/G	0.5	0	upstream-variant-2KB, utr-variant-5-prime	Hectd2, LOC105246565	GRCm38.p3	19:36554162	GCCAGGAGAGGACAC[A/G]GGGAAAGAGTTAGTC	226098
rs31044706	snp	A/C	0.359862	0.224567	intron-variant	Hectd2	GRCm38.p3	19:36595124	TCTGGCTTCTCAGTT[A/C]TTACAAACACATAAT	226098
rs31075415	snp	C/G	0.375	0.216506	intron-variant	Hectd2	GRCm38.p3	19:36586457	CGAAGGAGTTGTGAC[C/G]CATTGGTTGAGAACT	226098
rs31094642	snp	C/T	0.375	0.216506	intron-variant	Hectd2	GRCm38.p3	19:36617735	AAGAACTGTCATCCC[C/T]TCTATAAGGCACACT	226098
rs31095513	snp	C/T	0.375	0.216506	intron-variant	Hectd2	GRCm38.p3	19:36575603	GCCTACACCTCTGTG[C/T]GCTCTTAACCATCTA	226098
rs31137403	snp	G/T	0.375	0.216506	intron-variant	Hectd2	GRCm38.p3	19:36566109	TAGGAACACAGACAG[G/T]AAGGAACCTGGAACA	226098
rs31163762	snp	G/T	0.444444	0.157135	intron-variant	Hectd2	Mm_Celera	19:36604059	GATTTTGGTACCTAC[G/T]GGCTACTAGGGTTCC	226098
rs31184459	snp	A/G	0.375	0.216506	upstream-variant-2KB, downstream-variant-500B	Hectd2, LOC105246565	Mm_Celera	19:36552730	CTATATAGAGCTCCC[A/G]GCAGAATAAACCAAT	226098
rs31196757	snp	A/T	0.493827	0.0552116	utr-variant-3-prime, nc-transcript-variant	Hectd2, 1500017E21Rik	GRCm38.p3	19:36620175	GCATTTAGTACCAGC[A/T]TATGGCCCATGTGCA	226098
rs31205527	snp	A/G	0.375	0.216506	intron-variant	Hectd2	GRCm38.p3	19:36617751	TCTATAAGGCACACT[A/G]TTGAAGATTGATAGG	226098
rs31227666	snp	A/G	0.401235	0.199068	intron-variant	Hectd2	GRCm38.p3	19:36584202	ATATTAGACAAAAGT[A/G]AAGACACAAAAGACA	226098
rs31240218	snp	A/T	0.46875	0.121031	intron-variant	Hectd2	GRCm38.p3	19:36601047	TGATTAATAAATTGC[A/T]TATTCATTTGAACAT	226098
rs31282759	snp	C/T	0.375	0.216506	intron-variant	Hectd2	Mm_Celera	19:36594001	TTCCATTTTCAAGTA[C/T]TGAACAGTTTTATTC	226098
rs31301780	snp	A/G	0.375	0.216506	intron-variant	Hectd2	GRCm38.p3	19:36593080	CAGTGCCCAATAAAT[A/G]TTGATTCCTGTTGTT	226098
rs36240105	snp	C/T	0.260355	0.249785	intron-variant	Hectd2	Mm_Celera	19:36596465	TGACTTTTATGGAAA[C/T]GTATGAAATGTATAC	226098
rs36241859	snp	A/G	0.277778	0.248452	intron-variant	Hectd2	Mm_Celera	19:36588987	GAACAAGTGAGAAAC[A/G]GTGGTCAGACTTGGG	226098
rs36250511	snp	C/G	0.497041	0.0383476	intron-variant	Hectd2	GRCm38.p3	19:36607147	TGAAGCTGTGTGGAA[C/G]AGAGGGAAGTTGCAG	226098
rs36258980	snp	C/T	0.152778	0.230321	intron-variant	Hectd2	Mm_Celera	19:36595175	GTGAAGTTAAACACT[C/T]ATCTGTAATCAATCA	226098
rs36269472	snp	A/G	0.260355	0.249785	intron-variant	Hectd2	Mm_Celera	19:36598469	AGGAGCACGGCATGA[A/G]CACTGAAACCAGGGT	226098
rs36274882	snp	A/G	0.497041	0.0383476	intron-variant	Hectd2	Mm_Celera	19:36582615	AATTGCAAGTTCCCC[A/G]ATTATAAAAATACAA	226098
rs36280695	snp	A/C	0.132653	0.220748	intron-variant	Hectd2	Mm_Celera	19:36578026	CATCTTACTTCATTG[A/C]GCCTTCGTGTTTAGC	226098
rs36281261	snp	A/G	0.260355	0.249785	intron-variant	Hectd2	Mm_Celera	19:36616592	TACAGCTCCTTCTCC[A/G]TGTCGCTGACCTGGC	226098
rs36294266	snp	A/G	0.244898	0.249948	intron-variant	Hectd2	Mm_Celera	19:36601627	TAGTGTAATCAGGAA[A/G]TGTTAAAAATATCAT	226098
rs36296687	snp	A/G	0.142012	0.225474	intron-variant	Hectd2	Mm_Celera	19:36580645	CATGTTTTCACAAAT[A/G]TATTTTTGCTTTTTT	226098
rs36309787	snp	C/T	0.231111	0.249285	intron-variant	Hectd2	Mm_Celera	19:36587117	AATTGTTGCTGGTCA[C/T]CAAAAGATCACCTTG	226098
rs36316831	snp	A/G	0.142012	0.225474	intron-variant	Hectd2	Mm_Celera	19:36617634	ATTGATTAAGTATAA[A/G]ATTAAATATAACTGT	226098
rs36317045	snp	G/T	0.244898	0.249948	intron-variant	Hectd2	Mm_Celera	19:36599065	TTCTCGCACTCTTCC[G/T]TTTCTCTTGAGAAGG	226098
rs36325254	snp	A/G	0.152778	0.230321	intron-variant	Hectd2	Mm_Celera	19:36594843	TCACTTCAGGAGTGG[A/G]CTATAAGCTGAAGTG	226098
rs36336976	snp	G/T	0.132653	0.220748	intron-variant	Hectd2	Mm_Celera	19:36588479	TTCACTATGCAGATA[G/T]AGGATGAGAACTGGT	226098
rs36347243	snp	A/C/G	0.277778	0.248452	intron-variant	Hectd2	Mm_Celera	19:36587252	TAGTGTCGCTCTCTA[A/C/G]TCACTAAGTCTACTT	226098
rs36350597	snp	A/G	0.260355	0.249785	intron-variant	Hectd2	Mm_Celera	19:36558595	GAAAACACAAGGTGT[A/G]TGCAGAGGACAAGAG	226098
rs36355545	snp	A/G	0.142012	0.225474	intron-variant	Hectd2	Mm_Celera	19:36578214	TCTTCAAAAACGTCC[A/G]TTTGTTCTTTTGTTT	226098
rs36356935	snp	A/G	0.444444	0.157135	intron-variant	Hectd2	Mm_Celera	19:36568849	GTTTTAGGAATTTTT[A/G]GAGTTGTTGAGATGG	226098
rs36359206	snp	A/C	0.132653	0.220748	intron-variant	Hectd2	Mm_Celera	19:36579014	TTCCAGAACTGTCCG[A/C]AGAGCATGTTGTAGA	226098
rs36377686	snp	C/G	0.132653	0.220748	intron-variant	Hectd2	Mm_Celera	19:36612497	TTAAGTATCATAGTA[C/G]ATAAGCTTTTAAAAG	226098
rs36381255	snp	A/T	0.152778	0.230321	intron-variant	Hectd2	Mm_Celera	19:36594815	GCTTGTTGCCAGTTT[A/T]CAGATATTTCTGTCA	226098
rs36383651	snp	A/T	0.5	0	intron-variant	Hectd2	Mm_Celera	19:36567758	TCAAGCCCTGTAATG[A/T]GTAAGGACTCTAGTG	226098
rs36404468	snp	A/T	0.124444	0.216185	intron-variant	Hectd2	Mm_Celera	19:36611105	TAACACCTGTTTGCT[A/T]AAGAGTGGGCTGTAG	226098

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