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
rs3662869	snp	A/G	0.359862	0.224567	intron-variant	Eml4	GRCm38.p3	17:83467962	GAGCGCTCTAGTACA[A/G]GGCAGCAGGCAGGTT	78798
rs6160797	snp	G/T	0.444444	0.157135	intron-variant	Eml4	Mm_Celera	17:83431803	GCCCCTCAAATAAAT[G/T]TTAAATAACCAATAT	78798
rs6250827	snp	C/T	0.5	0	intron-variant	Eml4	GRCm38.p3	17:83358648	tgcacagtCAGACAG[C/T]GCAGTGAACACATAA	78798
rs6250849	snp	A/T	0.391111	0.206368	intron-variant	Eml4	Mm_Celera	17:83358675	ATAATGAGAACAAAT[A/T]CTGCCAGTAGACATT	78798
rs6251413	snp	A/C	0.5	0	intron-variant	Eml4	Mm_Celera	17:83358815	GTTTTTGAGAGAAAA[A/C]TACAACAAAGAATAT	78798
rs6251786	snp	A/G	0.5	0	intron-variant	Eml4	Mm_Celera	17:83358841	AATATTATTGAATCA[A/G]CACTGGAGTTTACAT	78798
rs6251859	snp	A/G	0.5	0	intron-variant	Eml4	Mm_Celera	17:83358894	TTATATCAGTGTTTA[A/G]CTTACTAACATTGAT	78798
rs6252346	snp	A/G	0.5	0	intron-variant	Eml4	Mm_Celera	17:83358980	AGTTGGTAGGGAGAC[A/G]GAACCATGGTGTCTG	78798
rs6253932	snp	C/T	0.359862	0.224567	intron-variant	Eml4	Mm_Celera	17:83359300	TACTGTTCTTGCAGC[C/T]TTTCTGTGACCCTGG	78798
rs6254374	snp	A/T	0.5	0	intron-variant	Eml4	Mm_Celera	17:83359337	CCAATACAGGGTTTT[A/T]NAAAATTGTATAAAT	78798
rs6254375	snp	A/T	0.5	0	intron-variant	Eml4	Mm_Celera	17:83359338	CAATACAGGGTTTTN[A/T]AAAATTGTATAAATg	78798
rs6263123	snp	A/G	0.48	0.0979796	intron-variant	Eml4	GRCm38.p3	17:83398260	CCTTGAGAAAAGAAT[A/G]GAAAGCACTAGCTTT	78798
rs6263530	snp	C/T	0.336735	0.234472	intron-variant	Eml4	Mm_Celera	17:83398286	GCTTTTCGTGGACAG[C/T]AATTTAAAATAGTGC	78798
rs6263545	snp	A/G	0.48	0.0979796	intron-variant	Eml4	Mm_Celera	17:83398295	GGACAGCAATTTAAA[A/G]TAGTGCCTCCTAAAA	78798
rs6384615	snp	C/T	0.5	0	intron-variant	Eml4, LOC105246332	Mm_Celera	17:83384788	tatctatctatctat[C/T]tatctatctTACACC	78798
rs6385160	snp	A/G	0.48	0.0979796	intron-variant	Eml4, LOC105246332	Mm_Celera	17:83384858	TCAAGTCTGTGTAGG[A/G]CTAGGTACATCTTCT	78798
rs6385657	snp	C/G	0.5	0	intron-variant	Eml4	Mm_Celera	17:83351548	AGCACCTTCTTCTGA[C/G]CCCCCCACCCCGTTA	78798
rs6387872	snp	A/G	0.5	0	intron-variant	Eml4	Mm_Celera	17:83352007	AGAAAGGGATAGGGT[A/G]TCCTGTTGGCTGAAG	78798
rs13472008	snp	G/T			utr-variant-3-prime	Eml4	Mm_Celera	17:83478969	GAAAACAAACCACAT[G/T]CCTTTAACAGATGAA	78798
rs13472009	snp	C/T	0.415225	0.187619	missense	Eml4	GRCm38.p3	17:83477922	GCCAGGCCGTCTAAC[C/T]CTCCTCCACTGCCTC	78798
rs13472010	snp	C/T	0.387812	0.208586	utr-variant-3-prime	Eml4	Mm_Celera	17:83479848	ACTTCTTCAGTTTAG[C/T]CTTCACCCAGGGTCA	78798
rs13472011	snp	G/T			missense	Eml4	Mm_Celera	17:83477817	ATGAGCATCATTCAG[G/T]GGAAGCTTGTGGAAA	78798
rs13483135	snp	A/G	0.499889	0.00746186	missense	Eml4	GRCm38.p3	17:83478060	AGCGAGTGGGGTAGC[A/G]AAGACCTTGGTGTGG	78798
rs29497264	snp	C/T	0.375	0.216506	missense	Eml4	Mm_Celera	17:83451039	TGATCTGGAGCAAAA[C/T]GATGGTAGAGCCCCC	78798
rs29497871	snp	A/G	0.444444	0.157135	intron-variant	Eml4, LOC105246332	GRCm38.p3	17:83383101	TTTTATTTTATGTGT[A/G]TAGGCAGTTTGCCTG	78798
rs29497974	snp	C/T	0.444444	0.157135	intron-variant	Eml4, LOC105246332	Mm_Celera	17:83383571	TTAATAATAGTCTTA[C/T]TATTGTTGGTACATA	78798
rs29498274	snp	C/T	0.387812	0.208586	intron-variant	Eml4	Mm_Celera	17:83367717	ATCCATATAATGATG[C/T]TACTTCTTGTTGTTT	78798
rs29498292	snp	C/T	0.444444	0.157135	utr-variant-3-prime	Eml4	GRCm38.p3	17:83480200	GGGATTATGAAACTG[C/T]TTTTGTTTTGTTGGG	78798
rs29498312	snp	A/C	0.375	0.216506	intron-variant	Eml4	Mm_Celera	17:83469150	AATTGTTTTGATTTT[A/C]ACTTGCATTACCATC	78798
rs29499117	snp	C/T	0.444444	0.157135	upstream-variant-2KB	Eml4	Mm_Celera	17:83350686	TCTAGCAGCAGGACA[C/T]CCACGAGCCCCGTCC	78798
rs29499533	snp	C/T	0.497041	0.0383476	intron-variant	Eml4	Mm_Celera	17:83396943	TACTTTTTTGTGAAT[C/T]TGTTGTTTAGTTGAC	78798
rs29499572	snp	A/G	0.345679	0.230967	intron-variant	Eml4	Mm_Celera	17:83443589	TGATGGAGACAGGCC[A/G]TGCTCAGGCTGGCTG	78798
rs29500109	snp	C/T	0.5	0	intron-variant	Eml4	GRCm38.p3	17:83353134	TTCTGGAGTTGCCTT[C/T]GCTGAAGAGACTTTG	78798
rs29500478	snp	C/G/T	0.375	0.216506	intron-variant	Eml4	GRCm38.p3	17:83421360	ACCTGTCCTGTGGCC[C/G/T]GGAGGGTGGCCAGAT	78798
rs29500531	snp	A/T	0.444444	0.157135	intron-variant	Eml4	GRCm38.p3	17:83400193	AAGTGTAAAACTCTT[A/T]TGTCAAGCACATTTG	78798
rs29500594	snp	C/T	0.498615	0.0262793	intron-variant	Eml4	GRCm38.p3	17:83426565	CTCCTGGAAATGTGC[C/T]TGTCCTTCTAGATTG	78798
rs29502305	snp	G/T	0.444444	0.157135	downstream-variant-500B	Eml4	Mm_Celera	17:83480491	CATGCCCTACATGCA[G/T]TTCTTTGGTTTTTCC	78798
rs29502406	snp	G/T	0.375	0.216506	intron-variant	Eml4	GRCm38.p3	17:83406182	GTTGGTTGGTTGGTT[G/T]TTTTGAGACAGGGTT	78798
rs29503428	snp	A/G	0.408163	0.193609	intron-variant	Eml4	GRCm38.p3	17:83456578	ACTTTGTACATTTGT[A/G]GAACATTAATTATGA	78798
rs29504275	snp	A/G	0.32	0.24	intron-variant, upstream-variant-2KB	Eml4, LOC105246332	GRCm38.p3	17:83392610	GTTTTGTGTTTGTTT[A/G]TTCATTTGTTTTAAA	78798
rs29504490	snp	A/G	0.32	0.24	intron-variant, nc-transcript-variant	Eml4, LOC105246332	Mm_Celera	17:83391664	GGCAGCCAGCATAGC[A/G]CTATTGTCTACTGTG	78798
rs29505066	snp	C/T	0.375	0.216506	intron-variant	Eml4	Mm_Celera	17:83362321	TGGATAGATGCCTGC[C/T]TGCCTGCCCGCCTGC	78798
rs29505074	snp	C/T	0.375	0.216506	intron-variant	Eml4	GRCm38.p3	17:83444899	AGTACTGACCATGAC[C/T]AGCTCATGCACATGC	78798
rs29505981	snp	A/C	0.401235	0.199068	intron-variant, upstream-variant-2KB	Eml4	Mm_Celera	17:83432802	ACCCAATTTCACAAA[A/C]CCTCAAAGCAAAGCA	78798
rs29506662	snp	A/G	0.32	0.24	intron-variant	Eml4	Mm_Celera	17:83407010	CTAGGTTTGGTTAGC[A/G]CTTGACAGGCAGAAT	78798
rs29510978	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	Eml4	Mm_Celera	17:83433605	CTTTTTCTCTTCTTT[A/G]TGTTTTTCAAAGACA	78798
rs29512275	snp	A/C	0.32	0.24	intron-variant	Eml4	Mm_Celera	17:83397087	CACATGAAAAAAAAA[A/C]CATTATATTCATTGT	78798
rs29512279	snp	A/G	0.359862	0.224567	intron-variant	Eml4	GRCm38.p3	17:83476870	AGTAACTTGCTAAGT[A/G]TATTGGTATGCCTTC	78798
rs29512486	snp	A/G	0.5	0	intron-variant	Eml4	GRCm38.p3	17:83400879	CTCTACAGTGTGTTC[A/G]TTCTGTAGTCAGCAT	78798
rs29514709	snp	C/T	0.375	0.216506	intron-variant	Eml4	Mm_Celera	17:83438841	CATGTATATACCACA[C/T]ATTTTCCCATTGCTT	78798
rs29518031	snp	C/T	0.32	0.24	intron-variant, upstream-variant-2KB	Eml4, LOC105246332	GRCm38.p3	17:83392896	GTTTCCAGAGCTCTT[C/T]CCAGCAGCATGAAAT	78798
rs29518577	snp	A/G	0.444444	0.157135	upstream-variant-2KB	Eml4	Mm_Celera	17:83350622	GAACTCTAGAACTGT[A/G]CTCCGCGGGCTTCCC	78798
rs29518620	snp	G/T	0.5	0	intron-variant	Eml4	GRCm38.p3	17:83400915	TGTGATTATAAATAT[G/T]CACTGGCCTTTTTAT	78798
rs29518792	snp	A/G	0.401235	0.199068	utr-variant-3-prime	Eml4	Mm_Celera	17:83479151	AGTGTAATAGTCACA[A/G]TGCCGCTTATAGGCT	78798
rs29519269	snp	C/T	0.492188	0.0620098	intron-variant	Eml4	GRCm38.p3	17:83426221	CCATCTTTAGAATTT[C/T]AGTAAAGTAAATGAC	78798
rs29519673	snp	C/T	0.32	0.24	intron-variant, nc-transcript-variant	Eml4, LOC105246332	Mm_Celera	17:83391181	TAAACATGCAAGTTG[C/T]TCTTCCAGAGGACCC	78798
rs29519888	snp	C/T	0.375	0.216506	intron-variant	Eml4	Mm_Celera	17:83452054	CTTTAAGTAACAGGG[C/T]GGCTGAATTAAGAAC	78798
rs29520176	snp	C/T	0.375	0.216506	intron-variant	Eml4, LOC105246332	Mm_Celera	17:83386136	GTGGCAGTTGGGATA[C/T]ACCAAAGAGCACTGG	78798
rs29520177	snp	C/T	0.345679	0.230967	intron-variant	Eml4	Mm_Celera	17:83370023	GGACGGTTAAGGAAG[C/T]ACTAATAACTTCATA	78798
rs29520272	snp	C/T	0.5	0	intron-variant	Eml4	GRCm38.p3	17:83468776	TGCGGTTCTCAGTCC[C/T]CTCTCTGTCTCTGCC	78798
rs29520294	snp	C/T	0.375	0.216506	intron-variant, nc-transcript-variant	Eml4, LOC105246332	Mm_Celera	17:83379118	TCAGAAAGTTAGGTG[C/T]CATTGTAGACTCATA	78798
rs29520423	snp	A/G	0.465374	0.126941	intron-variant	Eml4	GRCm38.p3	17:83449440	CAAATGAAGAATAAC[A/G]TGTCACAGTCTCCTG	78798
rs29520515	snp	G/T	0.444444	0.157135	intron-variant	Eml4	Mm_Celera	17:83355563	ACAAGAAAAGCACAT[G/T]CTTTTGTCCTTTAGG	78798
rs29521285	snp	C/T	0.48	0.0979796	intron-variant	Eml4, LOC105246332	GRCm38.p3	17:83387092	TCTATCTTCCGCATA[C/T]GTGCTATGGTACTGC	78798
rs29521945	snp	C/T	0.375	0.216506	intron-variant	Eml4	Mm_Celera	17:83464102	TAATTAAATCAATCT[C/T]TTTTAAAAATAAAAT	78798
rs29522358	snp	A/G	0.33241	0.236027	synonymous-codon	Eml4	Mm_Celera	17:83477960	ACCGTTAACTGGGAC[A/G]GCTGAAGAGGAAAGC	78798
rs29523158	snp	C/G/T	0.375	0.216506	upstream-variant-2KB	Eml4	GRCm38.p3	17:83349875	CTCTAATCTGCACAT[C/G/T]GACCTAGAAGGGACC	78798
rs29523159	snp	A/C	0.32	0.24	intron-variant	Eml4	Mm_Celera	17:83363201	CCTCCTGGAGTTGGA[A/C]ATTGAGAGTTAAAAG	78798
rs29523220	snp	C/T	0.444444	0.157135	intron-variant	Eml4, LOC105246332	Mm_Celera	17:83383382	CATATATATATATCT[C/T]GTTTACATCTCATCC	78798
rs29523770	snp	A/G	0.375	0.216506	intron-variant	Eml4	Mm_Celera	17:83357429	GGATTAAAGGTGTTC[A/G]CCACATGCTCAGTGT	78798
rs29524954	snp	A/G	0.444444	0.157135	intron-variant	Eml4	Mm_Celera	17:83366449	CACAGGGAGTCTGGG[A/G]AGTCAGGAACTTTAT	78798
rs29529550	snp	C/T	0.444444	0.157135	intron-variant	Eml4	Mm_Celera	17:83475642	CCTCCTTCCTCCTCC[C/T]TCCTCCTCCCTCCTC	78798
rs29532967	snp	A/T	0.5	0	intron-variant	Eml4	Mm_Celera	17:83445611	AATAAGTAAATATTT[A/T]AAAAAAATTCTTTGG	78798
rs29533100	snp	G/T	0.375	0.216506	intron-variant	Eml4	Mm_Celera	17:83418830	CCTTCCTTGACCAAG[G/T]TATCATTGAGAAGAG	78798
rs29533460	snp	C/T	0.375	0.216506	intron-variant	Eml4	Mm_Celera	17:83368875	GCCATTTTGTTGGGT[C/T]TAGGATTGAACTCAG	78798
rs29535529	snp	A/T	0.32	0.24	intron-variant	Eml4	GRCm38.p3	17:83452530	GCCTGCTCACTGTTT[A/T]CACTCTTTTCCTTCC	78798
rs29535739	snp	A/T	0.375	0.216506	intron-variant	Eml4	GRCm38.p3	17:83401284	CAACTATGATTTTTT[A/T]AAAAATCCTCCCAAT	78798
rs29536199	snp	C/T	0.5	0	intron-variant	Eml4	Mm_Celera	17:83412860	TGTCGTGGAATACTT[C/T]GGATCCTACTCATCA	78798
rs29536358	snp	G/T	0.375	0.216506	intron-variant	Eml4	Mm_Celera	17:83352528	AAATCATTGTTGTTA[G/T]ACAGCTTTGAGAATG	78798
rs29536647	snp	A/G	0.345679	0.230967	synonymous-codon	Eml4	Mm_Celera	17:83477915	TGAAACTGCCAGGCC[A/G]TCTAACTCTCCTCCA	78798
rs29536655	snp	C/T	0.375	0.216506	intron-variant, nc-transcript-variant	Eml4, LOC105246332	GRCm38.p3	17:83391761	GTATGTGGTACCTTC[C/T]GCAATAAGTCCTTAC	78798
rs29538202	snp	A/G	0.444444	0.157135	intron-variant	Eml4	GRCm38.p3	17:83354821	TAGGAGTGTTCTACT[A/G]CATCAAGCCCTTTTA	78798
rs29538913	snp	A/G	0.444444	0.157135	intron-variant	Eml4	Mm_Celera	17:83470303	CTCTGCCTCCCAAGT[A/G]CTGAGATTAAAGCTG	78798
rs29539175	snp	G/T	0.359862	0.224567	intron-variant	Eml4	GRCm38.p3	17:83467396	TAGTAAAGAAGCCAC[G/T]CCATAGTCCGGCTAA	78798
rs29540022	snp	A/C	0.444444	0.157135	intron-variant	Eml4	Mm_Celera	17:83352166	TTACTGTAGAGATTT[A/C]AGTGTTACGGTGAGA	78798
rs29540635	snp	C/T	0.32	0.24	intron-variant	Eml4	Mm_Celera	17:83356380	CCACTTTGTTTCTTA[C/T]AAAATGGCAGTTTTG	78798
rs29542156	snp	A/C	0.32	0.24	intron-variant	Eml4, LOC105246332	Mm_Celera	17:83386654	TGATTGAAGACTCAG[A/C]CCACTATGGGCAGTG	78798
rs33043618	snp	A/T	0.375	0.216506	intron-variant	Eml4	Mm_Celera	17:83357652	ACAAGACCAACATTT[A/T]AAAAGACGAAGGGAG	78798
rs33043912	snp	G/T	0.375	0.216506	intron-variant	Eml4	Mm_Celera	17:83352707	TTTGTTCTTTTTTGG[G/T]TTTGTGACTGGGTTC	78798
rs33044219	snp	A/G	0.345679	0.230967	intron-variant	Eml4	Mm_Celera	17:83467533	GGTGTGAAGAGAGTG[A/G]GGATCTAAGGGTGCT	78798
rs33046486	snp	C/T	0.486111	0.0821678	intron-variant	Eml4	GRCm38.p3	17:83366445	GGCTCACAGGGAGTC[C/T]GGGAAGTCAGGAACT	78798
rs33046839	snp	G/T	0.375	0.216506	intron-variant	Eml4	Mm_Celera	17:83439636	TGTTGTTTAGGTTGA[G/T]TAAGTAGTGTGATAA	78798
rs33048002	snp	G/T	0.375	0.216506	intron-variant	Eml4, LOC105246332	GRCm38.p3	17:83382352	TCTTCCAGCCAAGTG[G/T]TAGCAGATTGTGTAT	78798
rs33048462	snp	C/G	0.32	0.24	intron-variant	Eml4, LOC105246332	GRCm38.p3	17:83387114	TGGTACTGCTTTGCT[C/G]TGCTTGACTGAAGCT	78798
rs33056234	snp	A/G	0.277778	0.248452	intron-variant	Eml4, LOC105246332	Mm_Celera	17:83381091	ATACCTCTTCTTACA[A/G]TCTCACATGTTTTGG	78798
rs33056577	snp	G/T	0.32	0.24	intron-variant	Eml4	GRCm38.p3	17:83464735	AGACATCAGACTCCT[G/T]ACCTGAATTTCACTT	78798
rs33057302	snp	C/T	0.33241	0.236027	intron-variant	Eml4	Mm_Celera	17:83451638	GAGCCTTCCAGCTGT[C/T]CTCCCTGGTCAGGCG	78798
rs33059771	snp	C/T	0.32	0.24	intron-variant	Eml4	Mm_Celera	17:83363111	CGAGAGGGTCAAATA[C/T]TTGAACATTTGGTCC	78798
rs33059773	snp	A/G	0.444444	0.157135	intron-variant	Eml4	Mm_Celera	17:83462148	ATATAACTTCATTCA[A/G]CATTGAGTAATTATT	78798
rs33060497	snp	A/G	0.444444	0.157135	intron-variant	Eml4, LOC105246332	Mm_Celera	17:83380716	GAAGTAAAAATTTAT[A/G]AAAGAAAATATTAAG	78798

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