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
rs31224336	snp	C/T	0.32	0.24	intron-variant	Gm21964	Mm_Celera	8:110106931	CTGGGACTCAGGGCT[C/T]ACTTGCTCCACACTT	102638837
rs31224339	snp	C/T	0.336735	0.234472	intron-variant	Gm21964	Mm_Celera	8:110107262	CACATAGACAGCTAA[C/T]CCTTGGCAGGTTGCT	102638837
rs31224342	snp	A/T	0.132653	0.220748	intron-variant	Gm21964	Mm_Celera	8:110107317	AGCCTTTTATGAGAG[A/T]CACAGATTGAGACTC	102638837
rs31225275	snp	A/G	0.124444	0.216185	intron-variant	Gm21964	Mm_Celera	8:110107391	GCTACCCATGTCCCC[A/G]AGGTTTTTGTTAGAT	102638837
rs31225278	snp	C/T	0.124444	0.216185	intron-variant	Gm21964	Mm_Celera	8:110107440	GGAGCTTCCCAGGGA[C/T]GTATCTAGGGTTAGC	102638837
rs31225281	snp	A/G	0.132653	0.220748	intron-variant	Gm21964	Mm_Celera	8:110107492	ATCTTTCTAAACAGG[A/G]CACTGGCTTGTCTTA	102638837
rs31226114	snp	C/T	0.124444	0.216185	intron-variant	Gm21964	Mm_Celera	8:110107608	CTTCATGTGTGACAC[C/T]GTTCCCATCTTAGAG	102638837
rs31226117	snp	A/G	0.132653	0.220748	intron-variant	Gm21964	Mm_Celera	8:110107652	TAGCAAATGTCAATG[A/G]CTGGCAGGCCAAGTC	102638837
rs31226120	snp	A/G	0.124444	0.216185	intron-variant	Gm21964	GRCm38.p3	8:110107870	AGTGAGTTTGATTTT[A/G]TCTACGCAGAAACAG	102638837
rs31226123	snp	A/C	0.124444	0.216185	intron-variant	Gm21964	GRCm38.p3	8:110107910	GCAAAACTTAGTTGA[A/C]AGTCAATCTTTGGAG	102638837
rs31227006	snp	C/T	0.132653	0.220748	intron-variant	Gm21964	Mm_Celera	8:110108294	GTTTCTCTGTGGCTG[C/T]GACTGAGCTGCATAC	102638837
rs31227009	snp	C/G	0.415225	0.187619	missense	Gm21964	Mm_Celera	8:110108986	CCCTGTTTGTCAGGA[C/G]ATGCACAGTATGATG	102638837
rs31227012	snp	C/G	0.132653	0.220748	intron-variant	Gm21964	Mm_Celera	8:110109691	GGAGTGTCCCTGAGC[C/G]AAACTCTTATGAGAA	102638837
rs31227057	snp	A/G	0.132653	0.220748	upstream-variant-2KB	Gm21964	Mm_Celera	8:110099790	GCTTGTCCAAACCCC[A/G]AAAATCTCATCTTGA	102638837
rs31227060	snp	A/G	0.124444	0.216185	upstream-variant-2KB	Gm21964	Mm_Celera	8:110099819	GAGACTGGCGGGAAG[A/G]AAGATCACCTTCTCC	102638837
rs31227063	snp	A/C	0.336735	0.234472	upstream-variant-2KB	Gm21964	Mm_Celera	8:110100254	TAAAGGCAGGAGTGG[A/C]GCTAGGTCCACAGGA	102638837
rs31227965	snp	G/T	0.124444	0.216185	synonymous-codon	Gm21964	Mm_Celera	8:110110242	CTACTCATTGGCCCT[G/T]TCCTCTGATGCTCAC	102638837
rs31227968	snp	C/T	0.231111	0.249285	intron-variant	Gm21964	Mm_Celera	8:110111414	TGAAGATGTGTGCAC[C/T]GAAACTCTCAGAGCC	102638837
rs31227971	snp	A/G	0.336735	0.234472	intron-variant	Gm21964	Mm_Celera	8:110111571	CCATGACACGGGGAA[A/G]CCCTGGGTCTACATA	102638837
rs31228026	snp	C/T	0.244898	0.249948	upstream-variant-2KB	Gm21964	Mm_Celera	8:110100307	GGCCAGGGAGTACTC[C/T]ACCCGTCTTTAGCTC	102638837
rs31228029	snp	C/G	0.244898	0.249948	upstream-variant-2KB	Gm21964	Mm_Celera	8:110100343	CGTGGACCCCAAGAT[C/G]TGCTTTCTGCTCCCT	102638837
rs31228032	snp	G/T	0.132653	0.220748	upstream-variant-2KB	Gm21964	Mm_Celera	8:110100743	CAAAGACTTTTTTCT[G/T]TTTCTACACTGTAAC	102638837
rs31228814	snp	A/G	0.231111	0.249285	downstream-variant-500B, upstream-variant-2KB	Gm21964, Gm35543	Mm_Celera	8:110112015	AGAGCAAAACTTGGA[A/G]TACCGATTGTGTGTT	102638837
rs31228817	snp	A/G	0.244898	0.249948	downstream-variant-500B, upstream-variant-2KB	Gm21964, Gm35543	Mm_Celera	8:110112340	TGAGAAAGAGACACA[A/G]AGAGAATCCAGTTGC	102638837
rs31228845	snp	A/G	0.260355	0.249785	upstream-variant-2KB	Gm21964	Mm_Celera	8:110101019	CTGACCAGAAAGCGA[A/G]GAGCATTCAGTTCTG	102638837
rs31228848	snp	A/G	0.132653	0.220748	utr-variant-5-prime	Gm21964	Mm_Celera	8:110101350	TCATCTACCATAGCA[A/G]GGCGGGTCTTCAAAT	102638837
rs31228851	snp	C/T	0.132653	0.220748	intron-variant	Gm21964	GRCm38.p3	8:110102631	TTCTGTGACCTCAGC[C/T]TACTCTTTACCGCCC	102638837
rs31229764	snp	G/T	0.124444	0.216185	intron-variant	Gm21964	Mm_Celera	8:110102751	GTTTTCATCAACAAA[G/T]GTCTAGGTGACTCTC	102638837
rs31229767	snp	A/G	0.124444	0.216185	intron-variant	Gm21964	Mm_Celera	8:110102794	TGTTGAAAGAGAAGC[A/G]CCTGCACTGGGAGAC	102638837
rs31229770	snp	C/G	0.124444	0.216185	intron-variant	Gm21964	Mm_Celera	8:110103096	TGACTGGCCCTTCTA[C/G]GGTTGTAAAGGCAAG	102638837
rs31229773	snp	C/T	0.42	0.183303	intron-variant	Gm21964	Mm_Celera	8:110103409	CGGCTTTCCTAAGAC[C/T]GGAGGCGATGTAATC	102638837
rs31230626	snp	A/T	0.132653	0.220748	intron-variant	Gm21964	Mm_Celera	8:110104113	TTTCTGTGAGAATCA[A/T]TAAAGAGGTATTTAC	102638837
rs31230629	snp	A/C	0.124444	0.216185	intron-variant	Gm21964	Mm_Celera	8:110104671	AGTCAAGGGATGGAA[A/C]GGAAATCAGAGTAGA	102638837
rs31230632	snp	A/C	0.132653	0.220748	intron-variant	Gm21964	Mm_Celera	8:110104841	CATGGTGCTCTAACC[A/C]ACAGCAGCAGCGGCA	102638837
rs31231625	snp	C/T	0.124444	0.216185	intron-variant	Gm21964	Mm_Celera	8:110105602	CCCAGAGGCTCATGT[C/T]CCTGAAGTTTCTCAC	102638837
rs31231628	snp	C/T	0.132653	0.220748	intron-variant	Gm21964	Mm_Celera	8:110105635	TATCCGTTGAATATA[C/T]GTGGAGAGATTCCAC	102638837
rs31231631	snp	A/G	0.231111	0.249285	intron-variant	Gm21964	Mm_Celera	8:110106039	GAAGTCACAAGTCCT[A/G]ATTAAGGCGTCTCAC	102638837
rs31232534	snp	A/T	0.132653	0.220748	intron-variant	Gm21964	Mm_Celera	8:110106040	AAGTCACAAGTCCTG[A/T]TTAAGGCGTCTCACT	102638837
rs31232537	snp	C/T	0.124444	0.216185	intron-variant	Gm21964	Mm_Celera	8:110106054	GATTAAGGCGTCTCA[C/T]TGGCTTTAAGTTTTA	102638837
rs31232540	snp	A/C	0.124444	0.216185	intron-variant	Gm21964	Mm_Celera	8:110106401	TGTTCCTATTTTCCA[A/C]TTTCTATATTGAAAC	102638837
rs31232543	snp	C/T	0.124444	0.216185	intron-variant	Gm21964	Mm_Celera	8:110106424	ATTGAAACACAGCTA[C/T]TCGTCTTAATCTCTT	102638837
rs33258406	snp	A/G	0.444444	0.157135	missense, intron-variant	Gm21964	Mm_Celera	8:110110649	AGCTGCAGCAACACA[A/G]CTTATGCCATGAGGT	102638837
rs48837452	snp	A/C			intron-variant	Gm21964	Mm_Celera	8:110110769	GTCTTGAGGTGTGGC[A/C]CTGGCAGTCTTGAAT	102638837
rs49595998	snp	G/T			intron-variant	Gm21964	Mm_Celera	8:110110767	GGGTCTTGAGGTGTG[G/T]CCCTGGCAGTCTTGA	102638837
rs211704085	snp	A/C			intron-variant	Gm21964	Mm_Celera	8:110103040	TTAGCTTCCACGGAC[A/C]TCATTTGACTGTATT	102638837
rs211806607	snp	C/G			intron-variant	Gm21964	Mm_Celera	8:110102591	TTTGTGTCTCCTCCC[C/G]GACCCCCCCCCCCCC	102638837
rs211910768	in-del	-/CCCC			intron-variant	Gm21964	GRCm38.p3	8:110102594	GTGTCTCCTCCCCGA[-/CCCC]CCCCCCCCCCACCCC	102638837
rs212444953	snp	C/T			intron-variant	Gm21964	Mm_Celera	8:110111405	TGGGGGGAATGAAGA[C/T]GTGTGCACCGAAACT	102638837
rs212767224	snp	A/G			intron-variant	Gm21964	Mm_Celera	8:110108176	TGAGCACATGTGTAT[A/G]TGCATATGCATGTGA	102638837
rs212802309	snp	G/T			intron-variant	Gm21964	Mm_Celera	8:110101594	TCTTTCCCTCACCCA[G/T]GGTGGGACCACCCAT	102638837
rs212927862	snp	A/T			intron-variant	Gm21964	Mm_Celera	8:110105486	GTTTGGTTGCCTTGG[A/T]GGCTGGCGATCTGCC	102638837
rs213048050	snp	C/T			upstream-variant-2KB	Gm21964	Mm_Celera	8:110100833	TAGGGATCAGTACAT[C/T]TGTCCCAGGAGTGGA	102638837
rs214078732	in-del	-/AAACTCTGAT			intron-variant	Gm21964	Mm_Celera	8:110105399	CTAGTGGTGAACTAG[-/AAACTCTGAT]AAAAGACAGGTGTAA	102638837
rs214092082	snp	C/T			intron-variant	Gm21964	Mm_Celera	8:110104163	GGACAGGGATTTATG[C/T]GAAGTTCCCTCCTGG	102638837
rs214203340	in-del	-/G			intron-variant	Gm21964	Mm_Celera	8:110104748	GAGTAGGAGTGTCCA[-/G]ACTCACCAGCAACTG	102638837
rs214345053	snp	A/G			intron-variant, downstream-variant-500B	Gm21964	Mm_Celera	8:110111057	AGAGTGAAGCAGGGA[A/G]GTACAGGGAGACAGA	102638837
rs214491667	snp	C/T			upstream-variant-2KB	Gm21964	Mm_Celera	8:110100638	ACACCTGCCAAACCT[C/T]TACTGAGCCTCCTCA	102638837
rs214498422	snp	A/C			intron-variant	Gm21964	Mm_Celera	8:110102542	TTCTGGAAGGACCCT[A/C]TTGTACACTGCTCAG	102638837
rs214633786	snp	A/T			intron-variant	Gm21964	Mm_Celera	8:110104713	GGTGAGAGGACAGGC[A/T]TGGGACAGATGAGGG	102638837
rs214709386	snp	A/C			intron-variant	Gm21964	Mm_Celera	8:110101798	GTGGGTCTGGGGGTG[A/C]CCTGCATAGGGAGGA	102638837
rs214780652	snp	A/G			intron-variant	Gm21964	Mm_Celera	8:110109464	GTACCTTAATATTAC[A/G]TTTTCAATACCCAGG	102638837
rs215143884	snp	C/T			upstream-variant-2KB	Gm21964	Mm_Celera	8:110099939	TTACAGGTTTAATTC[C/T]CTCTCTTCCTACAAG	102638837
rs215332505	snp	C/G			intron-variant	Gm21964	Mm_Celera	8:110105437	GCAGGAAGAAGGAGA[C/G]GGGATGGCCCCCTCC	102638837
rs215391028	snp	C/G			intron-variant	Gm21964	Mm_Celera	8:110104975	GTTTTGAAACCATTG[C/G]TACCACTACCACCAC	102638837
rs215636103	snp	C/T			intron-variant	Gm21964	Mm_Celera	8:110103789	CAGCACTCAGTACAT[C/T]GAGGCAAGTGGATCT	102638837
rs216187752	snp	C/T			intron-variant	Gm21964	Mm_Celera	8:110107341	GAGACTCCTGTCATA[C/T]CTGATGATCTGAATG	102638837
rs216452531	snp	A/G			intron-variant	Gm21964	Mm_Celera	8:110109300	GATGGCAGATGAGGT[A/G]CCCAGTTTGGTGTTA	102638837
rs216509344	snp	C/T			intron-variant	Gm21964	Mm_Celera	8:110108224	GGCACTCGAGGAGGC[C/T]AGAGGGTAGCCTTTC	102638837
rs216523990	snp	A/G			intron-variant	Gm21964	Mm_Celera	8:110102475	CAAAGGACCAGATGA[A/G]TATGGAGGAGATGAA	102638837
rs216584501	snp	G/T			intron-variant	Gm21964	Mm_Celera	8:110101708	ACGCCATTCTCAGAG[G/T]GGGGGCCTCGTGCAG	102638837
rs217286985	snp	C/G			intron-variant	Gm21964	Mm_Celera	8:110106203	GCCCGATGCCTCTCA[C/G]AGAAAATATATTAAC	102638837
rs217564022	snp	C/T			intron-variant	Gm21964	Mm_Celera	8:110104319	AGTTCCTCAAGGATG[C/T]AGGCTTGGCTTTGGC	102638837
rs217654028	snp	A/C			intron-variant	Gm21964	Mm_Celera	8:110105364	CTCTAGACAAGACAG[A/C]CACAGAAATGCAAGG	102638837
rs217708489	snp	A/T			intron-variant	Gm21964	Mm_Celera	8:110104807	GAAGAGCTGTGTAGG[A/T]TGTGTAGAGCATCTC	102638837
rs217982176	in-del	-/G/GG/GGG/TTGG			intron-variant	Gm21964	GRCm38.p3	8:110108151	ATACTCCACTTTTTT[-/G/GG/GGG/TTGG]GGGGGGGGGTGAGCA	102638837
rs218104597	snp	C/T			downstream-variant-500B, upstream-variant-2KB	Gm21964, Gm35543	Mm_Celera	8:110112087	GCAAGTGGGGGCATG[C/T]CATTCTTCCAAGGTG	102638837
rs218203991	snp	C/T			intron-variant	Gm21964	Mm_Celera	8:110108373	CCACCTTGCTGTACA[C/T]GTGCAGAGATTATAG	102638837
rs218332101	snp	A/T			intron-variant	Gm21964	Mm_Celera	8:110109628	GATAAGTAGTCTCTA[A/T]AGCCCACAGGGTAAC	102638837
rs219294353	in-del	-/A			downstream-variant-500B, upstream-variant-2KB	Gm21964, Gm35543	Mm_Celera	8:110112148	ATAGAATACCCTGAC[-/A]AAAAAAGCAACTTAG	102638837
rs219432804	in-del	-/G			intron-variant	Gm21964	Mm_Celera	8:110101882	TGGAGCAACTCGCCT[-/G]GCCGCTTCCAGCAAG	102638837
rs219992180	snp	C/T			upstream-variant-2KB	Gm21964	Mm_Celera	8:110100963	CCTCTGAAATCTCCC[C/T]ACCCTCCAGACCACT	102638837
rs220601639	snp	G/T			upstream-variant-2KB	Gm21964	Mm_Celera	8:110101112	TCTTGGCCTTTTTTT[G/T]GGGGGGGGGGTGCGG	102638837
rs220619577	snp	C/T			upstream-variant-2KB	Gm21964	Mm_Celera	8:110100155	TCTTCCCATCTCCCC[C/T]AACCTCCTGTGAACC	102638837
rs220779601	snp	C/T			upstream-variant-2KB	Gm21964	Mm_Celera	8:110099449	AACCACAGAGGTACC[C/T]GGAAGGGGACACTCT	102638837
rs220856702	snp	A/C			intron-variant	Gm21964	Mm_Celera	8:110106384	TTCCCCCTTCCATTC[A/C]TTGTTCCTATTTTCC	102638837
rs220893833	snp	A/G			intron-variant	Gm21964	Mm_Celera	8:110101839	AGCAGCCATTTAGGA[A/G]TCCTCTTTCGCTCCT	102638837
rs221068942	snp	A/G			intron-variant	Gm21964	Mm_Celera	8:110105706	TGTGGCCACACCCTG[A/G]TATTGACCAGCCATT	102638837
rs221089046	snp	C/T			intron-variant	Gm21964	Mm_Celera	8:110104390	ATGATTACAAGTGAC[C/T]GGGGAACATCATTCC	102638837
rs221351118	snp	C/G			upstream-variant-2KB	Gm21964	Mm_Celera	8:110100019	CCCAGCACCCAGCAC[C/G]AGCCACTAATGTACA	102638837
rs221532567	snp	A/G			synonymous-codon	Gm21964	Mm_Celera	8:110109789	CCAGCCTCCCATTCC[A/G]GATGAGGCAGTGGTC	102638837
rs221623586	snp	G/T			intron-variant	Gm21964	Mm_Celera	8:110101966	GCCACACGAAGGCTC[G/T]TTCTCTGCTCGGAAC	102638837
rs221714975	snp	A/G			intron-variant	Gm21964	Mm_Celera	8:110102696	CACTGTATGAGGAAG[A/G]CAGGAAGTGTTTGGT	102638837
rs221768435	snp	C/T			intron-variant	Gm21964	Mm_Celera	8:110103337	GAACATTTACATCAT[C/T]ACATGTTACCAGCCT	102638837
rs222065237	snp	A/G			intron-variant	Gm21964	Mm_Celera	8:110105074	CTCTGCCACGTTACC[A/G]TCACTGTCACCACCC	102638837
rs222217573	snp	C/T			intron-variant	Gm21964	Mm_Celera	8:110110476	CCGGGTTGTGGGGGT[C/T]GGGGGCAAACATTTC	102638837
rs222347282	snp	A/G			intron-variant	Gm21964	Mm_Celera	8:110107475	GGGTAGGTTGGAGTG[A/G]AATCTTTCTAAACAG	102638837
rs222424711	snp	A/G			upstream-variant-2KB	Gm21964	Mm_Celera	8:110100875	CGTCCAAAACCCGTC[A/G]CCCCCCAGAAAATGT	102638837
rs222484285	snp	C/T			upstream-variant-2KB	Gm21964	Mm_Celera	8:110100090	AGCCCTTGTTACCCC[C/T]GAATAAAGAAAGCTG	102638837
rs222512598	snp	C/T			intron-variant	Gm21964	Mm_Celera	8:110103234	AATGCACACAAATAC[C/T]AACACAAAATCCACC	102638837
rs222556223	snp	C/T			intron-variant	Gm21964	Mm_Celera	8:110105166	CATCTCAACAACCCC[C/T]GTTATCCCCATCATC	102638837

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