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
rs6276641	snp	A/G	0.5	0	intron-variant	Cyld	Mm_Celera	8:88703006	ctgttcattgtgggg[A/G]aaaaaaaggcctctc	74256
rs6408031	snp	A/G	0.5	0	intron-variant	Cyld	Mm_Celera	8:88728590	TGCTTTTTTTCTGTG[A/G]AACCTTGTTACATCT	74256
rs13459668	snp	G/T			utr-variant-3-prime	Cyld	GRCm38.p3	8:88751116	GAGGGGCTTTCCCTT[G/T]CTCCTGTGTGAGAAT	74256
rs13471428	snp	A/C			missense	Cyld	Mm_Celera	8:88741315	TCAAAAAGTTCAAGA[A/C]TGTAACTTCTATCAA	74256
rs13471429	snp	A/G	0.484429	0.0868505	utr-variant-3-prime	Cyld	Mm_Celera	8:88747473	TCTGCCTTTACTCCA[A/G]TTGTTGAAGGTGTGC	74256
rs32557099	snp	A/G	0.487535	0.077957	utr-variant-3-prime	Cyld	Mm_Celera	8:88747457	ATGATTTTATTAAGA[A/G]TCTGCCTTTACTCCA	74256
rs32562540	snp	A/G	0.444444	0.157135	synonymous-codon, intron-variant	Cyld	GRCm38.p3	8:88730799	GCCTGTTTCCAATCA[A/G]ATTGAAAGGTGTAAC	74256
rs32579907	snp	C/T	0.5	0	intron-variant	Cyld	Mm_Celera	8:88740695	ATGTTACAGTGTTCA[C/T]TGTGATGGGAATTTG	74256
rs32587816	snp	A/G	0.5	0	intron-variant	Cyld	GRCm38.p3	8:88738830	TGGGAAAGGCACCTG[A/G]GCAATTCTTTATCCT	74256
rs32588689	snp	C/T	0.5	0	intron-variant	Cyld	Mm_Celera	8:88701229	TTTGTGTTCAGTACC[C/T]CTCTAGAATTTGTCT	74256
rs32598398	snp	C/T	0.465374	0.126941	intron-variant	Cyld	Mm_Celera	8:88746181	AGAACCCTAGTAGCA[C/T]CTCCTTGACCAGGGA	74256
rs32603165	snp	A/C	0.5	0	intron-variant	Cyld	GRCm38.p3	8:88726337	CTCAAAAGCCCACCC[A/C]TAGTGATACATCTCC	74256
rs32616032	snp	A/G	0.5	0	intron-variant	Cyld	GRCm38.p3	8:88715801	TAGTGAGCGCATCTG[A/G]CCGGTCATTGTTGTT	74256
rs32616518	snp	C/T	0.465374	0.126941	intron-variant	Cyld	GRCm38.p3	8:88741271	GATAGCTTATGTGCA[C/T]TTCTTTTTGATACTC	74256
rs32618656	snp	A/G	0.5	0	intron-variant	Cyld	GRCm38.p3	8:88703248	TAGGCATGTTGGGTT[A/G]ACTTGCTTGCTGGGT	74256
rs32623502	snp	C/T	0.42	0.183303	intron-variant	Cyld	GRCm38.p3	8:88720022	TTGAGGAATTATTGT[C/T]TCCTTTTGACAGAAC	74256
rs32627408	snp	C/T	0.5	0	intron-variant	Cyld	GRCm38.p3	8:88739878	CAGGGCCATCCAAGC[C/T]CCTTGTAGCACCAGT	74256
rs32634773	snp	G/T	0.484429	0.0868505	intron-variant	Cyld	Mm_Celera	8:88742282	TTATTTTTATTATTT[G/T]TAGGCACCATCATGC	74256
rs32655308	snp	C/T	0.465374	0.126941	intron-variant	Cyld	GRCm38.p3	8:88742159	TGCAGGAGACAAGAC[C/T]CAAAGCTGTGGGCAT	74256
rs32671734	snp	A/T	0.465374	0.126941	intron-variant	Cyld	GRCm38.p3	8:88746359	TGTAATCCAGTCATC[A/T]AAGCACACAAAGTAA	74256
rs32686567	snp	A/G	0.5	0	intron-variant	Cyld	Mm_Celera	8:88741655	TTTAGGTGCAAAATG[A/G]GGAGGAAATCTAGTG	74256
rs32689435	snp	A/T	0.375	0.216506	intron-variant	Cyld	GRCm38.p3	8:88725094	TGGGAAGAAGTCATC[A/T]GAGGCTCAACTGGGA	74256
rs32693202	snp	A/C	0.456747	0.140554	intron-variant	Cyld	Mm_Celera	8:88745935	CATGGTTTGCATTTA[A/C]CTCATTCTTCCTGAT	74256
rs32694325	snp	C/T	0.48	0.0979796	intron-variant	Cyld	GRCm38.p3	8:88720083	AGATTTGTTAGCTAT[C/T]ACTATCAGCTGCCTG	74256
rs32695977	snp	A/G	0.465374	0.126941	intron-variant	Cyld	GRCm38.p3	8:88745637	AACAGATTTGTTAAA[A/G]AGTGCTGTCTAAGAT	74256
rs32698743	snp	C/T	0.465374	0.126941	intron-variant	Cyld	GRCm38.p3	8:88735317	TTTGGAGTTGCCTCT[C/T]CTCCTGTGGTGAGGG	74256
rs32705103	snp	C/T	0.46875	0.121031	intron-variant	Cyld	GRCm38.p3	8:88720578	TTCTTCTGATTTAAC[C/T]ATCACCCTATAAACC	74256
rs32708228	snp	A/G	0.444444	0.157135	intron-variant	Cyld	Mm_Celera	8:88734625	TAATAATAAGCAAAT[A/G]TTATTGATTAAAAAC	74256
rs32719302	snp	A/G	0.444444	0.157135	intron-variant	Cyld	Mm_Celera	8:88744539	GGCAGGATTAATATA[A/G]TAAAAATGGCTATCT	74256
rs32728805	snp	A/G	0.444444	0.157135	intron-variant	Cyld	GRCm38.p3	8:88746457	CATAGGAAAACAGCA[A/G]TGGGCATTACTAGGT	74256
rs32734620	snp	C/T	0.489796	0.070696	intron-variant	Cyld	GRCm38.p3	8:88706986	TGCAACTGTTAGTCA[C/T]GGTATTTCTTATTAT	74256
rs32741510	snp	A/T	0.33241	0.236027	intron-variant	Cyld	GRCm38.p3	8:88721721	GCTAGGACCATCTAC[A/T]GGCTGCCCCAGAGGT	74256
rs32744947	snp	A/G	0.473373	0.11227	intron-variant	Cyld	Mm_Celera	8:88702931	GAGGGAGTAGTATAA[A/G]TGTTCTGCTTAGAGC	74256
rs32760514	snp	A/C	0.48	0.0979796	intron-variant	Cyld	Mm_Celera	8:88706893	GTCTAACTCTTTCAC[A/C]AAAGAATTATGATTT	74256
rs32763244	snp	A/G	0.5	0	upstream-variant-2KB	Cyld	GRCm38.p3	8:88695086	GAAAGATGAAGAACT[A/G]CAAATAGTATCTAGT	74256
rs32781530	snp	C/G	0.48	0.0979796	intron-variant	Cyld	GRCm38.p3	8:88720074	AGATTCCTGAGATTT[C/G]TTAGCTATTACTATC	74256
rs32797037	snp	C/T	0.444444	0.157135	utr-variant-3-prime	Cyld	Mm_Celera	8:88747982	TCTTAACTGCTGAGC[C/T]ATCTCTCTAGCCCCA	74256
rs32797868	snp	A/G	0.48	0.0979796	intron-variant	Cyld	GRCm38.p3	8:88735362	TCAACTCCCCCACCT[A/G]CGCTTCTAGTTGAAC	74256
rs32803540	snp	A/G	0.444444	0.157135	intron-variant	Cyld	Mm_Celera	8:88700374	TTTAATGTGTTTCAA[A/G]CATACTTTTTTCTTT	74256
rs32806205	snp	A/G	0.5	0	intron-variant	Cyld	Mm_Celera	8:88721791	AATTTTACTGGTAAA[A/G]TTCTAAGATGTTTAA	74256
rs32821698	snp	C/T	0.5	0	intron-variant	Cyld	GRCm38.p3	8:88735563	GTCTACTGAAATCCT[C/T]CAAAAGACATAAAAA	74256
rs32828134	snp	C/T	0.5	0	intron-variant	Cyld	Mm_Celera	8:88704094	GTTAAAACTGTGACA[C/T]AAACTCCACAATTTA	74256
rs32829012	snp	A/G	0.375	0.216506	intron-variant	Cyld	Mm_Celera	8:88739725	GTGAGCCCCTGGAAA[A/G]AAATGAATAAACAAG	74256
rs32830813	snp	A/G	0.465374	0.126941	intron-variant	Cyld	Mm_Celera	8:88740119	GCTTGTCATAGTGGA[A/G]AATGTACAACCCAAC	74256
rs32832677	snp	C/T	0.5	0	intron-variant	Cyld	GRCm38.p3	8:88727364	TTTTTTTCATTGTTT[C/T]GTTTTTGTTTTGTCA	74256
rs32832883	snp	C/T	0.5	0	intron-variant	Cyld	GRCm38.p3	8:88697692	TAGTTGGAAGGTGCA[C/T]CCTGTTGAGACAGGT	74256
rs32837045	snp	A/G	0.484429	0.0868505	intron-variant	Cyld	GRCm38.p3	8:88739939	GAGCTGCAGGATCTG[A/G]GTATTCTCAGATGCG	74256
rs32841062	snp	A/T	0.444444	0.157135	intron-variant	Cyld	Mm_Celera	8:88706518	GGAAACATACCAAAA[A/T]TTTTTTTTGAGTATT	74256
rs32848853	snp	C/T	0.48	0.0979796	upstream-variant-2KB	Cyld	GRCm38.p3	8:88695406	GAGCATTCAACTATA[C/T]AAGATGTCACTATCA	74256
rs32850108	snp	C/T	0.444444	0.157135	intron-variant	Cyld	GRCm38.p3	8:88739124	ATGGCAGCATCCAGG[C/T]AGATGGTGCTGGAGA	74256
rs32854945	snp	G/T	0.444444	0.157135	intron-variant, utr-variant-5-prime, upstream-variant-2KB	Cyld	GRCm38.p3	8:88697411	GCTTGGGTAGGAGCA[G/T]TGCAGGACTCCGTCT	74256
rs32855010	snp	A/G	0.5	0	upstream-variant-2KB	Cyld	GRCm38.p3	8:88695110	ATCTAGTATGACAAT[A/G]ACATCATTTTTGTGT	74256
rs32855591	snp	C/T	0.444444	0.157135	intron-variant	Cyld	Mm_Celera	8:88740806	AGGGTCCCTGGGCTT[C/T]ACACCTTGTGCTGCT	74256
rs32862927	snp	A/G	0.48	0.0979796	intron-variant	Cyld	GRCm38.p3	8:88713938	ATTAACACATCTGAT[A/G]TGATACCACATCCAG	74256
rs32866894	snp	A/G	0.5	0	intron-variant	Cyld	GRCm38.p3	8:88717312	TGCTGTGTGTATACT[A/G]TGTATACTTGAGGTC	74256
rs32871456	snp	C/T	0.5	0	intron-variant	Cyld	Mm_Celera	8:88704198	GGCTATAAACCATTT[C/T]CAAATATTATTTATA	74256
rs32882167	snp	C/T	0.444444	0.157135	utr-variant-3-prime	Cyld	Mm_Celera	8:88751642	AACATTCATTTCTTT[C/T]ATATATATATATATA	74256
rs32886211	snp	A/C	0.465374	0.126941	intron-variant	Cyld	GRCm38.p3	8:88711457	ATGAAGGCTCCTGGG[A/C]TGCACTCTGTCCTTC	74256
rs32889277	snp	C/T	0.475309	0.108333	synonymous-codon	Cyld	GRCm38.p3	8:88746923	CCTGCACTCTTTGGA[C/T]TCCAGAAGGATTCAA	74256
rs32898290	snp	G/T	0.456747	0.140554	intron-variant	Cyld	Mm_Celera	8:88726907	AAGAATAGTGTGTAA[G/T]ACCCATAGGTTTTAA	74256
rs32899852	snp	A/G	0.375	0.216506	intron-variant	Cyld	Mm_Celera	8:88709527	TGAGCAAAGTGTCCA[A/G]GGATATAAATGTGTG	74256
rs32905495	snp	A/G	0.444444	0.157135	intron-variant	Cyld	GRCm38.p3	8:88715577	TCCACATGCTTCTCT[A/G]CTTCTTCCATCTCTT	74256
rs32905942	snp	C/T	0.5	0	intron-variant	Cyld	GRCm38.p3	8:88738842	CTGAGCAATTCTTTA[C/T]CCTCCCCCTCACACT	74256
rs32914066	snp	A/T	0.444444	0.157135	intron-variant	Cyld	Mm_Celera	8:88738594	GAAAAGCAAGAAAAA[A/T]AATCCTGAGAAAGAA	74256
rs32928999	snp	G/T	0.48	0.0979796	intron-variant	Cyld	Mm_Celera	8:88739849	AGAAGACACCAGTAC[G/T]ATGGCCACTAAGGCA	74256
rs32929887	snp	C/T	0.5	0	intron-variant	Cyld	GRCm38.p3	8:88699318	CTCAGAAGAGCCAGA[C/T]GTGATTGAATTACAC	74256
rs32947337	snp	G/T	0.408163	0.193609	intron-variant	Cyld	GRCm38.p3	8:88701402	AGAAAATGGCTGATT[G/T]CAAGAGAGACATTTA	74256
rs32948918	snp	C/T	0.48	0.0979796	intron-variant	Cyld	GRCm38.p3	8:88725932	AGCCTGATCATGCCC[C/T]ATCATTCCCAGCAGG	74256
rs32961348	snp	A/T	0.415225	0.187619	intron-variant	Cyld	GRCm38.p3	8:88742081	GAAACTACTGCTGGG[A/T]GTGACAGCTGTGACT	74256
rs32962875	snp	A/G	0.5	0	intron-variant	Cyld	Mm_Celera	8:88717303	ATGCAGTCCTGCTGT[A/G]TGTATACTGTGTATA	74256
rs32965142	snp	A/C	0.444444	0.157135	intron-variant	Cyld	GRCm38.p3	8:88700292	ATTTGGTTTTTCATC[A/C]GGTATGTGTGTAGAA	74256
rs32966074	snp	A/G	0.497041	0.0383476	intron-variant	Cyld	Mm_Celera	8:88712656	TTCTTTTGTACAGTC[A/G]TATCCTCTAGTGAAA	74256
rs32969265	snp	A/G	0.432133	0.171253	intron-variant	Cyld	GRCm38.p3	8:88730451	AGGGCAAATCAGTAA[A/G]CCAAGGAAATGCATG	74256
rs32982317	snp	A/T	0.48	0.0979796	intron-variant	Cyld	Mm_Celera	8:88698348	TTTTAAGGTATTCTT[A/T]AAAAAAAAAAAAAAA	74256
rs33005549	snp	C/T	0.5	0	intron-variant	Cyld	GRCm38.p3	8:88745662	TAAGATCTCAGCACT[C/T]GGGAGGTAGAGGATT	74256
rs33014361	snp	C/T	0.5	0	intron-variant	Cyld	Mm_Celera	8:88734380	TGACTAAAGTGTTAG[C/T]GACTCTAAAAAGCAA	74256
rs33015197	snp	A/G	0.465374	0.126941	intron-variant	Cyld	GRCm38.p3	8:88746337	GAATAAAACCAAACA[A/G]GCTTTCTGTAATCCA	74256
rs33015765	snp	C/T	0.5	0	intron-variant	Cyld	Mm_Celera	8:88738673	GAGAATGCTTAAAAT[C/T]GTTTTTAAAATTTTC	74256
rs33021583	snp	C/T	0.456747	0.140554	intron-variant	Cyld	GRCm38.p3	8:88711272	GATGTATTTTGTCTC[C/T]GGTTCTATAAAAGAT	74256
rs33025973	snp	C/T	0.48	0.0979796	downstream-variant-500B	Cyld	GRCm38.p3	8:88752179	CAGTCTCGAAGCCTC[C/T]GACCACAGGTTGCTC	74256
rs33031164	snp	C/T	0.444444	0.157135	intron-variant	Cyld	Mm_Celera	8:88740941	AGCATTTGCTTTAAT[C/T]ATTAAAAGCAGATTA	74256
rs33034753	snp	C/G	0.5	0	intron-variant	Cyld	Mm_Celera	8:88721816	GTTTAAATAGTAAAT[C/G]TAAAAAAAAATTAAG	74256
rs33042467	snp	C/T	0.465374	0.126941	intron-variant	Cyld	GRCm38.p3	8:88745486	TTCCTAGTGAGAACA[C/T]GTGTGTGAAGTAATA	74256
rs33046539	snp	A/G	0.5	0	intron-variant, utr-variant-5-prime	Cyld	GRCm38.p3	8:88697491	CCTGCCTGGCTCCCA[A/G]CGGCTGCAGGAGGCA	74256
rs33047815	snp	A/G	0.444444	0.157135	intron-variant	Cyld	GRCm38.p3	8:88697637	GTTTCTCTGGTCTGG[A/G]GGGAGGGGGGAGGAG	74256
rs33058373	snp	C/T	0.5	0	intron-variant	Cyld	GRCm38.p3	8:88735560	GTAGTCTACTGAAAT[C/T]CTTCAAAAGACATAA	74256
rs33066649	snp	C/T	0.444444	0.157135	intron-variant	Cyld	Mm_Celera	8:88744696	CAATAAAAGAACTTC[C/T]GGTGGAATCACCGTC	74256
rs33070571	snp	A/G	0.444444	0.157135	intron-variant	Cyld	GRCm38.p3	8:88744726	CCTTGACCTCAAGCT[A/G]TACTACAGAGCAATT	74256
rs33076738	snp	A/G	0.5	0	intron-variant	Cyld	Mm_Celera	8:88701014	AATAGGCAGGTACCA[A/G]TTTACCATCTAAAGA	74256
rs33077561	snp	C/T	0.444444	0.157135	intron-variant	Cyld	GRCm38.p3	8:88722046	TACTACCACACACCT[C/T]GCCTAAACCTGAATT	74256
rs33080513	snp	C/G	0.465374	0.126941	intron-variant	Cyld	GRCm38.p3	8:88741218	CTCAGGTCCTGCCAG[C/G]TGGCTTGATATTGTG	74256
rs33083024	snp	C/T	0.444444	0.157135	utr-variant-3-prime	Cyld	Mm_Celera	8:88747893	GAGGGCATCAGATCT[C/T]ATTACAGATGGTTGT	74256
rs33085981	snp	C/T	0.48	0.0979796	intron-variant	Cyld	GRCm38.p3	8:88723923	GAGGCCATGAAAGAA[C/T]GCTACTTACTAGCTT	74256
rs33184433	snp	A/G	0.5	0	intron-variant	Cyld	GRCm38.p3	8:88741657	TAGGTGCAAAATGGG[A/G]AGGAAATCTAGTGTT	74256
rs33185771	snp	G/T	0.444444	0.157135	intron-variant	Cyld	Mm_Celera	8:88733736	AAGAAAGTAAAAGAA[G/T]AAATTTCTCTATTTA	74256
rs33192148	snp	C/T	0.5	0	upstream-variant-2KB	Cyld	GRCm38.p3	8:88696251	TTGAAAGATCCTTCA[C/T]TATACCCTTAATTCT	74256
rs33202328	snp	A/G	0.465374	0.126941	intron-variant	Cyld	GRCm38.p3	8:88745464	CCTGTATTTAGGGGT[A/G]TAGTGCTTCCTAGTG	74256
rs33218755	snp	C/T	0.5	0	intron-variant	Cyld	GRCm38.p3	8:88738860	TCCCCCTCACACTTC[C/T]AAGCAACCTGTTCAT	74256
rs33221741	snp	A/G	0.48	0.0979796	intron-variant	Cyld	GRCm38.p3	8:88725204	CGTGTGCGTACACAT[A/G]CATGTGTATGTGTGT	74256
rs33253840	snp	C/G	0.5	0	intron-variant	Cyld	GRCm38.p3	8:88727339	TATGAATAAGATCCT[C/G]GTTTATTGGTTTTTT	74256

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