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
rs6267643	snp	C/G	0.5	0	intron-variant, upstream-variant-2KB	Seh1l, Gm26910	Mm_Celera	18:67775449	CATTCCTGTGGGCCT[C/G]GCCTGTGTTCCTCTG	72124
rs6269183	snp	A/T	0.5	0	intron-variant, downstream-variant-500B, upstream-variant-2KB	Seh1l, 4930549G23Rik, Gm26910	Mm_Celera	18:67775711	AATGTGCTACGATGT[A/T]TTTTTNTTTTTTTTT	72124
rs6269194	snp	A/T	0.5	0	intron-variant, downstream-variant-500B, upstream-variant-2KB	Seh1l, 4930549G23Rik, Gm26910	Mm_Celera	18:67775717	CTACGATGTNTTTTT[A/T]TTTTTTTTTTTTTtt	72124
rs13475476	snp	C/T	0.336735	0.234472	synonymous-codon, intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67785075	TAAGCTGTGCTGCAG[C/T]TGCATTTCCTGGAAC	72124
rs13475478	snp	A/G	0.32	0.24	missense, intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67784998	GATGGTATAGTAAGG[A/G]TCTACGAGGCTCCCG	72124
rs29540124	snp	G/T	0.48	0.0979796	intron-variant	Seh1l, 4930549G23Rik	GRCm38.p3	18:67781548	TCATACTCCTGTAAG[G/T]AACCCAAGCAAAGTC	72124
rs29541917	snp	A/T	0.375	0.216506	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67789839	TGAGTGTGAGTGTCT[A/T]CAACCCCCTGCTCCT	72124
rs29546554	snp	C/T	0.415225	0.187619	intron-variant	Seh1l, 4930549G23Rik	GRCm38.p3	18:67784792	AGAATGAAAACATAA[C/T]GAATGGCAGAGTTGC	72124
rs29553048	snp	A/G	0.444444	0.157135	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67778145	AGCCCCCCTCACCCC[A/G]CCCCAATCTGGTCTA	72124
rs29556753	snp	C/T	0.48	0.0979796	intron-variant, nc-transcript-variant	Seh1l, 4930549G23Rik	GRCm38.p3	18:67790824	ACCACTGTACCTGGT[C/T]GATTCTGTCACTGAC	72124
rs29559104	snp	A/G	0.5	0	intron-variant	Seh1l, 4930549G23Rik	GRCm38.p3	18:67786307	CCACCGAGAGCCACC[A/G]TGTATGTGGTGCTGG	72124
rs29578291	snp	C/G	0.375	0.216506	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67787086	GGTTGTCTGTCTCCT[C/G]GAGTCCAGGTCTGAA	72124
rs29580860	snp	C/T	0.5	0	intron-variant	Seh1l, 4930549G23Rik	GRCm38.p3	18:67786460	CTAATCCCAGCACTC[C/T]GGTGGCAGAGGCAGA	72124
rs29619112	snp	C/T	0.444444	0.157135	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67785119	CGCGGCCTTCTAAAG[C/T]GGCCAGGGCAGGTTG	72124
rs29624386	snp	A/G	0.444444	0.157135	intron-variant	Seh1l, 4930549G23Rik	GRCm38.p3	18:67790126	GTGCTACACTGAGGG[A/G]ACTTGGTACAATCAG	72124
rs29624843	snp	A/G	0.432133	0.171253	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67777923	TGTGAATGGATGAAT[A/G]CTTGCACATGTATCT	72124
rs29625596	snp	C/T	0.444444	0.157135	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67778889	GTAAAAAATGTTCTA[C/T]CTGATAGAGGAACCT	72124
rs29631613	snp	A/C	0.375	0.216506	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67787640	GAGACTTTATTTTAG[A/C]TAAGTTTTGATTAAG	72124
rs29671663	snp	C/T	0.444444	0.157135	utr-variant-3-prime, intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67793693	GTGATATTATCCACA[C/T]AATGACTTTACAGGT	72124
rs29676017	snp	A/C	0.277778	0.248452	intron-variant	Seh1l, 4930549G23Rik	GRCm38.p3	18:67785393	ATGCATAGAACTCAG[A/C]CATTTTCCTCAAGGA	72124
rs29721413	snp	C/G	0.375	0.216506	intron-variant	Seh1l, 4930549G23Rik	GRCm38.p3	18:67788508	TGCCTGCAGAGGCCA[C/G]AGAACAACATTTAGA	72124
rs29724676	snp	G/T	0.375	0.216506	intron-variant	Seh1l, 4930549G23Rik	GRCm38.p3	18:67780417	CTATTGCTCTAATAC[G/T]TCTTGCAGATAGGTC	72124
rs29769061	snp	C/T	0.5	0	intron-variant	Seh1l, 4930549G23Rik	GRCm38.p3	18:67788478	ATACGTGAGTACATG[C/T]CACCTATCTGCTGGT	72124
rs29769876	snp	C/T	0.48	0.0979796	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67790808	GGGATCACAAGGGCA[C/T]ACCACTGTACCTGGT	72124
rs29772278	snp	A/C	0.5	0	intron-variant	Seh1l, 4930549G23Rik	GRCm38.p3	18:67778391	TGGCTTAGATGGAAC[A/C]GGATGACTTCCTTTG	72124
rs29874904	snp	C/T	0.444444	0.157135	utr-variant-3-prime, intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67793696	ATATTATCCACACAA[C/T]GACTTTACAGGTGAT	72124
rs29921286	snp	A/T	0.456747	0.140554	intron-variant	Seh1l, 4930549G23Rik	GRCm38.p3	18:67787746	TTTTTCTTTACCTAT[A/T]AGTGATCTGTCCATG	72124
rs29924493	snp	A/T	0.375	0.216506	utr-variant-3-prime, intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67794432	ATGTCTCTGTAACAT[A/T]GGTACTGGTAATTTG	72124
rs29930204	snp	A/G	0.375	0.216506	intron-variant, downstream-variant-500B	Seh1l, 4930549G23Rik	Mm_Celera	18:67792648	TGTGTGTATAATAGT[A/G]TGTATAATAGTGGTA	72124
rs29930207	snp	C/T	0.444444	0.157135	utr-variant-3-prime, intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67793664	GTGATATTATCCACA[C/T]AACGACTTTACAGGT	72124
rs29948454	snp	C/T	0.475309	0.108333	intron-variant	Seh1l, 4930549G23Rik	GRCm38.p3	18:67784844	TCTTCAGATCCATCA[C/T]AGTCCTTTTCATGTA	72124
rs29960052	snp	C/G	0.375	0.216506	intron-variant, downstream-variant-500B	Seh1l, 4930549G23Rik	Mm_Celera	18:67792646	TTTGTGTGTATAATA[C/G]TGTGTATAATAGTGG	72124
rs29962587	snp	G/T	0.444444	0.157135	intron-variant	Seh1l, 4930549G23Rik	GRCm38.p3	18:67787964	TCCTGGAACTTACTC[G/T]GGAGACTACGCTAGC	72124
rs29962871	snp	A/G	0.290657	0.246672	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67789247	GAATATGTTAAGTGT[A/G]TTTATTTGTATTTCT	72124
rs29968659	snp	C/G	0.432133	0.171253	intron-variant	Seh1l, 4930549G23Rik	GRCm38.p3	18:67790205	TGAGCATCAGCTATA[C/G]AACTGCAGTGGGTCT	72124
rs29969577	snp	C/T	0.375	0.216506	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67779353	AAATGATAAACCTGA[C/T]ACAGTGTTTTCCTGA	72124
rs30014336	snp	A/G	0.277778	0.248452	intron-variant	Seh1l, 4930549G23Rik	GRCm38.p3	18:67788844	TGAGGTAAGTTGTAG[A/G]AAAATGAGGAATTTG	72124
rs30022451	snp	A/G	0.401235	0.199068	intron-variant	Seh1l, 4930549G23Rik	GRCm38.p3	18:67780551	AATTGGTCTAAAGAG[A/G]CCCTTAGGACTGTCA	72124
rs30054382	snp	C/T	0.32	0.24	intron-variant	Seh1l, 4930549G23Rik	GRCm38.p3	18:67781396	GAAAGAGTCAGCACA[C/T]CCTCCGTTGAAGCTG	72124
rs30057313	snp	A/G	0.444444	0.157135	intron-variant	Seh1l, 4930549G23Rik	GRCm38.p3	18:67781950	TCTTCAGACGAGCCA[A/G]AAGAGGGCATCAAAT	72124
rs30063692	snp	A/C	0.456747	0.140554	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67785314	AGTTAGGATATTTTT[A/C]GGAGACAGCTCTGTG	72124
rs30115838	snp	C/T	0.444444	0.157135	synonymous-codon, intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67788734	GACAGTCACAGACCC[C/T]GTCCATGATATCGCG	72124
rs30162285	snp	A/G	0.375	0.216506	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67778019	GTAGAAGAACACTGA[A/G]TACTCTTATATGCTG	72124
rs30170625	snp	A/G	0.48	0.0979796	intron-variant	Seh1l, 4930549G23Rik	GRCm38.p3	18:67781495	CCAGGCTGATGGGGG[A/G]CTTGGTGATACAGTT	72124
rs30255798	snp	A/G	0.444444	0.157135	upstream-variant-2KB, nc-transcript-variant	Seh1l, Gm26910	GRCm38.p3	18:67772912	GAAACAGCTGTGACT[A/G]TCTGCACAAGGCCTG	72124
rs30259887	snp	G/T	0.375	0.216506	intron-variant, downstream-variant-500B	Seh1l, 4930549G23Rik	Mm_Celera	18:67792653	GTATAATAGTGTGTA[G/T]AATAGTGGTAAAATA	72124
rs30265571	snp	A/T	0.375	0.216506	intron-variant, downstream-variant-500B	Seh1l, 4930549G23Rik	Mm_Celera	18:67792649	GTGTGTATAATAGTG[A/T]GTATAATAGTGGTAA	72124
rs30272570	snp	C/T	0.465374	0.126941	intron-variant	Seh1l, 4930549G23Rik	GRCm38.p3	18:67784879	TTAAATTGTATTTTT[C/T]TTTCCAGGTGAAGAG	72124
rs33851477	snp	A/G	0.375	0.216506	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67789871	TAGGGAACTGGGGGC[A/G]GAGAGAGAGGAGACT	72124
rs36249803	snp	A/C	0.231111	0.249285	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67784135	TGGCTCACACTGGTA[A/C]CCAGGCTTTTCCTTG	72124
rs36251681	snp	A/T	0.231111	0.249285	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67791761	ATACACAAATATTTT[A/T]AAAAATGTAGCCCAT	72124
rs36293392	snp	A/G	0.142012	0.225474	intron-variant, downstream-variant-500B	Seh1l, 4930549G23Rik	Mm_Celera	18:67792917	GATTTTGAGGTTTTA[A/G]GTATTTGCAACTATA	72124
rs36334418	snp	C/G	0.32	0.24	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67790148	TACAATCAGTGGACA[C/G]TGCCTTTGATGCCTG	72124
rs36352591	snp	A/G	0.231111	0.249285	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67784358	CTCAGTTGATCGTTA[A/G]CCTGTGTGCTGCTCA	72124
rs36363867	snp	A/G	0.132653	0.220748	utr-variant-3-prime, intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67793939	ATGGTATGATCCTAC[A/G]CATCTTCGTTTCTTT	72124
rs36378678	snp	A/G	0.231111	0.249285	utr-variant-3-prime, intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67793833	CCAAGCAGCACATTA[A/G]CATTTGCTAGTTTAG	72124
rs36399619	snp	C/G	0.124444	0.216185	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67777195	CTTTTAAAGAATGTC[C/G]TCAAGCTGGATGTGG	72124
rs36414048	snp	A/C	0.231111	0.249285	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67790258	TAAAATACAGTTTGG[A/C]TAAGCCTTGATGGCC	72124
rs36456619	snp	A/G	0.231111	0.249285	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67789687	TTTTATTTCTATGTG[A/G]AAGAAAGCCAGTTTT	72124
rs36517350	snp	A/T	0.231111	0.249285	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67782799	GATTATTGAATTTTT[A/T]AAAAATTGTGGTGAC	72124
rs36554714	snp	A/C	0.391111	0.206368	intron-variant	Seh1l, 4930549G23Rik	GRCm38.p3	18:67786606	ATAACCTGGAAGAGG[A/C]GAGAGATGTAGAGAA	72124
rs36579240	snp	A/T	0.124444	0.216185	intron-variant, downstream-variant-500B	Seh1l, 4930549G23Rik	Mm_Celera	18:67793004	GTAGAGTTAATTTTT[A/T]AAAATCTGGTTTTAG	72124
rs36579672	snp	C/T	0.231111	0.249285	utr-variant-3-prime, intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67794038	AGGATTTTTAATGTG[C/T]TGTTTCAATGAGTTC	72124
rs36591463	snp	A/C	0.124444	0.216185	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67786901	ATGCTTTAGTAACAA[A/C]GCTCTAGTTTAGTTT	72124
rs36600223	snp	C/T	0.231111	0.249285	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67778999	TGGGCTTAGTCTTCA[C/T]TACACCACTAGCCCC	72124
rs36611812	snp	C/T	0.142012	0.225474	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67788915	CAGTAAAGGCACAGG[C/T]CTGCAGACAGAGTCC	72124
rs36650920	snp	C/T	0.124444	0.216185	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67779012	CATTACACCACTAGC[C/T]CCTAATGGCAGTACC	72124
rs36693094	snp	C/T	0.124444	0.216185	intron-variant, upstream-variant-2KB	Seh1l, 4930549G23Rik, Gm26910	Mm_Celera	18:67776566	CTGTGCCTTCAGGAT[C/T]GCAGTCAGGTGTAGT	72124
rs36696234	snp	A/G	0.124444	0.216185	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67790021	TGTGGCACACGCTGA[A/G]ATAAAACACTCGCAC	72124
rs36769517	snp	C/T	0.231111	0.249285	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67788681	TTTTAATTCCTTTTT[C/T]TTTGAATTAGGAAAT	72124
rs36788602	snp	C/T	0.124444	0.216185	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67787834	TCTTTGCTGGCTCTT[C/T]CAGCGATTGAGCCCA	72124
rs36806552	snp	C/T	0.231111	0.249285	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67779325	ATTAATAATTTGGTG[C/T]TCATCTTTGAGAAAA	72124
rs36807222	snp	C/T	0.32	0.24	intron-variant, upstream-variant-2KB	Seh1l, 4930549G23Rik, Gm26910	Mm_Celera	18:67776514	GAGTTCCTCAAAGCT[C/T]GTGAGAGAGTAAAAA	72124
rs36875459	snp	A/T	0.231111	0.249285	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67780719	CAACATGACACAGGT[A/T]CACTGAGGACAGATT	72124
rs36898107	snp	C/T	0.231111	0.249285	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67782243	TTCCTATTATGTACA[C/T]CAACATGCCATGTGC	72124
rs36910368	snp	A/G	0.124444	0.216185	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67786808	GTTATGTGAATATTT[A/G]TTATAGATATACTCT	72124
rs36957289	snp	A/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Seh1l, 4930549G23Rik, Gm26910	Mm_Celera	18:67776847	TTATACACACTTTTT[A/T]AAAAAATCTGTGTAA	72124
rs37147162	snp	C/T	0.231111	0.249285	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67787346	CTGTTACCTGATTCA[C/T]TGTTTCCTGAGAGAT	72124
rs37207072	snp	A/G	0.124444	0.216185	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67781150	AATCCATAATTTTTC[A/G]CAAAAGCAGTTTCTG	72124
rs37207458	snp	A/T	0.231111	0.249285	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67780617	GTCCTCACAGAATGT[A/T]TACTTCTGCCTTATA	72124
rs37208007	snp	A/G	0.244898	0.249948	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67778346	AGCACTTCTTTTCCT[A/G]TCTGCATAAGTCTCC	72124
rs37283744	snp	A/G	0.124444	0.216185	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67781133	CATCTTTCCAGTCCC[A/G]GAATCCATAATTTTT	72124
rs37322033	snp	G/T	0.244898	0.249948	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67784199	CCAGATTTTGTGTAT[G/T]TGTGTATTTTATATG	72124
rs37341885	snp	A/G	0.231111	0.249285	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67791152	TGAAAACCTTAATGT[A/G]TTTCTTCTAAAGATT	72124
rs37360625	snp	C/T	0.124444	0.216185	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67789032	CTCTGTCTTGTAAAA[C/T]GTAACATCTGTTAGA	72124
rs37413998	snp	C/T	0.231111	0.249285	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67784681	CCCCTTTCTCTCTCT[C/T]ACAGTCATAAGTATT	72124
rs37439196	snp	C/T	0.444444	0.157135	intron-variant	Seh1l, 4930549G23Rik	GRCm38.p3	18:67781242	TTGCCGTCACAAAGC[C/T]GAGTTGCCTTGGTGA	72124
rs37504012	snp	A/G	0.32	0.24	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67791823	GTATTTATATGGATA[A/G]ATATTAGTCATGTTA	72124
rs37660022	snp	C/T	0.132653	0.220748	downstream-variant-500B, intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67795655	TAAAATGGATGCACT[C/T]TAAGATAATTTAGAC	72124
rs37675721	snp	C/T	0.132653	0.220748	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67778942	CATTAGTCAGAGTTC[C/T]CAGTAGAGCATTTGA	72124
rs37722010	snp	A/G	0.231111	0.249285	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67787722	TTCTTGGGCCAATCC[A/G]ACAGAATTTTTTTCT	72124
rs37835820	snp	A/C	0.32	0.24	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67789185	ATGGAATGATGTTCA[A/C]GTAGTCCGAAGGTTG	72124
rs38072233	snp	A/T	0.231111	0.249285	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67786879	GATTAGTGGATCTAA[A/T]TATGTGATGCTTTAG	72124
rs38077583	snp	C/T	0.124444	0.216185	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67790068	ACTTTCTGTCTCTCA[C/T]TCAAAGACTAAATCC	72124
rs38255725	snp	C/T	0.124444	0.216185	synonymous-codon, intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67784902	GTGAAGAGGACAACT[C/T]TAGTGGACAGCAGAA	72124
rs38306813	snp	A/C/G	0.124444	0.216185	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67781327	GTGATGGCTGACTCT[A/C/G]TGCTAATACAGAAGG	72124
rs38390891	snp	C/T	0.124444	0.216185	utr-variant-3-prime, intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67794303	TCTCAGTATCATGTA[C/T]GCACCTAGGAGGTGT	72124
rs38391664	snp	A/T	0.132653	0.220748	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67787377	TCCAAGTTCTGTGCT[A/T]TTTATACTTGGTGGT	72124
rs38494957	snp	C/T	0.336735	0.234472	intron-variant	Seh1l, 4930549G23Rik	GRCm38.p3	18:67790160	ACAGTGCCTTTGATG[C/T]CTGTAGCATCACAGT	72124
rs38765417	snp	A/T	0.32	0.24	intron-variant	Seh1l, 4930549G23Rik	Mm_Celera	18:67789325	TTTTTGAAAACTTTT[A/T]AAATCTTTTTTTAGG	72124

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