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
rs4170445	snp	G/T	0.444444	0.157135	upstream-variant-2KB	Tnk2	Mm_Celera	16:32642327	TACAGTCAGACACTT[G/T]GATGTGATTTCTGGC	51789
rs4170449	snp	A/C	0.444444	0.157135	intron-variant	Tnk2	Mm_Celera	16:32647078	AAAAAACCCAAAAAA[A/C]CAAAAATCATAAAAC	51789
rs4170450	snp	A/G	0.375	0.216506	intron-variant	Tnk2	Mm_Celera	16:32648323	TTATTTTTCCTTTCT[A/G]ACCTCTGTCTGCAAT	51789
rs4170451	snp	C/T	0.375	0.216506	intron-variant	Tnk2	GRCm38.p3	16:32653390	GCCTTCTCGATAGCC[C/T]AGTTTTTGATACTTT	51789
rs4170452	snp	C/T	0.444444	0.157135	intron-variant	Tnk2	Mm_Celera	16:32654889	CCCTTCCCCAGTTCC[C/T]CAGGAAGTCTGGGAT	51789
rs4170453	snp	C/T	0.30839	0.243086	intron-variant	Tnk2	GRCm38.p3	16:32656647	AAGAGTGAGTGGTGC[C/T]CAGGAAAGTGTGTCG	51789
rs4170454	snp	A/G	0.455	0.143091	intron-variant, upstream-variant-2KB	Tnk2	GRCm38.p3	16:32660296	TGGGGACAGACAAGA[A/G]AGCAGTATACAAGAA	51789
rs4170455	snp	G/T	0.484429	0.0868505	intron-variant, upstream-variant-2KB	Tnk2	GRCm38.p3	16:32660435	GAGCAGCTGGCACTT[G/T]TGAGGGGCATAGGGA	51789
rs4170456	snp	C/T	0.489796	0.070696	intron-variant, utr-variant-5-prime	Tnk2	GRCm38.p3	16:32661384	ATTTCTAGGACAGGT[C/T]CCCCCCCACCCCCAC	51789
rs4170457	snp	A/G	0.5	0	intron-variant	Tnk2	Mm_Celera	16:32662159	AGGGGAACGGGCTGT[A/G]CTATGTTTTCTAAGT	51789
rs4170458	snp	C/T	0.444444	0.157135	intron-variant	Tnk2	GRCm38.p3	16:32663246	TCCATACACATGCAC[C/T]ATGACAAGCAAACAT	51789
rs4170459	snp	C/T	0.459184	0.136902	intron-variant	Tnk2	GRCm38.p3	16:32663356	TGCCTGCCTCACAGT[C/T]CTTCATTGAAGAGCC	51789
rs4170460	snp	C/G	0.5	0	intron-variant, downstream-variant-500B	Tnk2, Tnk2os	GRCm38.p3	16:32664901	GGGTTGTGGCTAGAC[C/G]TCTCTTGCTAAAAGA	51789
rs4170461	snp	C/T	0.5	0	intron-variant, downstream-variant-500B	Tnk2, Tnk2os	GRCm38.p3	16:32665205	CGCAGCTGTGTGACA[C/T]CATGAGCAAAGCCGC	51789
rs4170462	snp	A/G	0.444444	0.157135	intron-variant	Tnk2, Tnk2os	GRCm38.p3	16:32667272	TTCTTTCTCTTTTCC[A/G]CCCATACCCCCACTT	51789
rs4170463	snp	A/G	0.35124	0.228584	intron-variant	Tnk2, Tnk2os	Mm_Celera	16:32667367	TCACTCAGCACACAC[A/G]GGTAAGGTTGGCCAG	51789
rs4170464	snp	G/T	0.476371	0.106096	intron-variant, nc-transcript-variant	Tnk2, Tnk2os	GRCm38.p3	16:32668009	TTGGGGTTAACTTCA[G/T]CCACAAGCAGCATCT	51789
rs4170465	snp	C/T	0.375	0.216506	intron-variant, upstream-variant-2KB	Tnk2, Tnk2os	Mm_Celera	16:32669077	CAAGGTGGGGGGCAT[C/T]CATAGATTATGGCAT	51789
rs4170466	snp	A/C/G	0.362812	0.2231	synonymous-codon, upstream-variant-2KB	Tnk2, Tnk2os	GRCm38.p3	16:32669479	CAATGCCATGCATTC[A/C/G]CTAGACCACCGAAAC	51789
rs4170467	snp	C/T	0.329861	0.236901	synonymous-codon, upstream-variant-2KB	Tnk2	Mm_Celera	16:32671562	CACTGACATGCGGGC[C/T]CTTCAGGACTTTGAG	51789
rs4170468	snp	C/G	0.444444	0.157135	intron-variant, upstream-variant-2KB	Tnk2	GRCm38.p3	16:32672206	GCCCCCTCCATCCAC[C/G]GCCCCGCCCTCCCGC	51789
rs4170469	snp	C/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Tnk2	GRCm38.p3	16:32672211	CTCCATCCACCGCCC[C/T]GCCCTCCCGCCCCAC	51789
rs4170470	snp	A/G	0.465374	0.126941	intron-variant, upstream-variant-2KB	Tnk2	GRCm38.p3	16:32672309	GCCTCCCTTGAACCA[A/G]CTTCCTATCTGCACC	51789
rs4170471	snp	C/T	0.493827	0.0552116	intron-variant	Tnk2	GRCm38.p3	16:32674156	TCTGGCCTAGTGCCC[C/T]GGGAAGTGTGGGGCT	51789
rs4170472	snp	C/T	0.35124	0.228584	intron-variant	Tnk2	Mm_Celera	16:32675224	TCTGGTAAATGTACC[C/T]GTCATGTCCCGTTTC	51789
rs4170473	snp	A/G	0.495868	0.0452663	intron-variant	Tnk2	GRCm38.p3	16:32678840	GGGTGTGTGCTGTGA[A/G]CTCTAGCTGCTGGAC	51789
rs4170474	snp	A/G	0.497622	0.0344007	synonymous-codon	Tnk2	GRCm38.p3	16:32679478	AACATACGACCCTGT[A/G]AGTGAGGACCCAGAC	51789
rs4170475	snp	C/G	0.444444	0.157135	missense	Tnk2	GRCm38.p3	16:32680322	CCTGGCAGCTCTCCA[C/G]TACCGCATCGGCTCT	51789
rs4170476	snp	C/T	0.375	0.216506	synonymous-codon	Tnk2	Mm_Celera	16:32680582	GCCGGCCGCCCTGCC[C/T]GTGCCCCCGCTGTTG	51789
rs4170477	snp	A/G	0.48	0.0979796	missense	Tnk2	GRCm38.p3	16:32680733	CCATCCCTGAGGGCC[A/G]CGGCTCGGCTGCCAC	51789
rs4170478	snp	A/G	0.387812	0.208586	synonymous-codon	Tnk2	GRCm38.p3	16:32682685	TTTCCTGTCTTTCAG[A/G]CGCTGATGGTTGACT	51789
rs6157656	snp	A/G	0.5	0	intron-variant	Tnk2	Mm_Celera	16:32654592	GCTAGACAGCTACGG[A/G]CATTTGNCCTTGGTC	51789
rs6157675	snp	A/G	0.5	0	intron-variant	Tnk2	Mm_Celera	16:32654599	AGCTACGGNCATTTG[A/G]CCTTGGTCACACATT	51789
rs32675406	snp	C/T	0.5	0	upstream-variant-2KB	Tnk2	Mm_Celera	16:32643361	CTTCCTTCCTTCCTT[C/T]CTTTCTTTCTTTCTT	51789
rs45651300	snp	C/T	0.336735	0.234472	intron-variant	Tnk2, Tnk2os	Mm_Celera	16:32666783	GTGATCAGTGGTCCT[C/T]TCTAAAATTGTCATG	51789
rs45705855	snp	A/C	0.486111	0.0821678	intron-variant, upstream-variant-2KB	Tnk2	GRCm38.p3	16:32660820	ACCAGGGTAACAGGG[A/C]CACATTAGCGTCTGA	51789
rs45724730	snp	C/T	0.336735	0.234472	intron-variant	Tnk2	Mm_Celera	16:32682614	GTGACCTTGGATTTC[C/T]GGTTAGCTGTTTAAC	51789
rs45762444	snp	A/G	0.244898	0.249948	intron-variant	Tnk2	Mm_Celera	16:32679170	ACGGGTATACATGGC[A/G]TGTTGCCTGCTCTAG	51789
rs45765502	snp	A/C	0.260355	0.249785	intron-variant, upstream-variant-2KB	Tnk2	GRCm38.p3	16:32658648	CGCTCTGGCTTCCTA[A/C]GGGTCGCGGCTGGCA	51789
rs45782206	snp	A/G	0.244898	0.249948	intron-variant	Tnk2, Tnk2os	Mm_Celera	16:32667394	CCAGCTCTGAGGGCA[A/G]CGAGAAGAGTCTGTA	51789
rs45812610	snp	C/G	0.260355	0.249785	intron-variant, missense	Tnk2	Mm_Celera	16:32661513	ATGCCGGCAGCCCGT[C/G]GGTTTCCTGGCCTTG	51789
rs45844593	snp	A/G	0.260355	0.249785	intron-variant	Tnk2	Mm_Celera	16:32662878	GAAGTCGTGTGAAGC[A/G]TTTACTGGTTGCAGT	51789
rs45914856	snp	C/T			intron-variant	Tnk2	Mm_Celera	16:32655834	TGAACCTTCGTCTTT[C/T]GGAAGAGCAGCCAGT	51789
rs45925987	snp	A/G	0.152778	0.230321	intron-variant, upstream-variant-2KB	Tnk2	Mm_Celera	16:32670715	GGCAGCTAAAGGGGT[A/G]GCAAGGAGAGGTCCC	51789
rs45965913	snp	A/G			intron-variant	Tnk2	GRCm38.p3	16:32661699	TCCTGAGGTCTGTGG[A/G]TTGGAGTGCTTTTCC	51789
rs45996840	snp	A/G			intron-variant	Tnk2	Mm_Celera	16:32655775	ATCCCTGGGACTGGA[A/G]TTCTAGACACTGTTG	51789
rs46008118	snp	A/G			intron-variant	Tnk2	GRCm38.p3	16:32656122	GGGTAGGTGGGAGGA[A/G]TGCTGAAGAGGTTAA	51789
rs46051275	snp	A/G	0.497041	0.0383476	intron-variant, upstream-variant-2KB	Tnk2	GRCm38.p3	16:32657993	GGAATGAGAAGGTGC[A/G]TGGGGTGCGCGCGCA	51789
rs46115656	snp	C/T	0.408163	0.193609	intron-variant	Tnk2	Mm_Celera	16:32651459	TTGGAGAGATGGCTT[C/T]GGTCTGGGCTTGGAT	51789
rs46144078	snp	C/T			intron-variant	Tnk2, Tnk2os	Mm_Celera	16:32667079	CCCTACCTGGCATAC[C/T]CTGCCCGCCCCACCC	51789
rs46175155	snp	A/G	0.35503	0.226867	intron-variant, nc-transcript-variant	Tnk2, Tnk2os	Mm_Celera	16:32666586	GGATTGGGCAGTAGA[A/G]ATTTTCTGGCTGCAG	51789
rs46194560	snp	C/T	0.260355	0.249785	intron-variant	Tnk2	Mm_Celera	16:32650920	GGTCTCCCTATGATG[C/T]AATCAGCGGTCAGGA	51789
rs46201794	snp	A/G	0.132653	0.220748	intron-variant, upstream-variant-2KB	Tnk2	Mm_Celera	16:32670626	ACTAGTGACCTCCAC[A/G]TTGCTGCTTAGCCTG	51789
rs46206746	snp	A/G	0.260355	0.249785	intron-variant	Tnk2	Mm_Celera	16:32670265	GGCTTGTAGGGCCCA[A/G]GCTCCACTCCAGTCT	51789
rs46229500	snp	A/T	0.277778	0.248452	intron-variant	Tnk2	Mm_Celera	16:32664490	CTCTAGTCCTTCCCC[A/T]TTGGTGTTTGATCAG	51789
rs46239983	snp	A/G	0.124444	0.216185	intron-variant	Tnk2	Mm_Celera	16:32673442	TGTCTTGTTGGATTA[A/G]GTCTGTCTGTGTGAC	51789
rs46307069	snp	A/G	0.142012	0.225474	intron-variant	Tnk2	Mm_Celera	16:32656201	CAGGATGCTGAGCAG[A/G]TATTGGAGTAGCTAC	51789
rs46377773	snp	C/T	0.35503	0.226867	intron-variant	Tnk2	Mm_Celera	16:32653162	TATACAGATTCAGGT[C/T]CTTGCACTTTTGCAG	51789
rs46474782	snp	C/G	0.375	0.216506	intron-variant, upstream-variant-2KB	Tnk2	GRCm38.p3	16:32658521	GTCTGTGGTTTCTTA[C/G]TTAACCCTCATATTG	51789
rs46474916	snp	A/G	0.260355	0.249785	intron-variant	Tnk2	Mm_Celera	16:32651940	AAGTCACGTTTAAAA[A/G]AAGATTGTGTTTTGA	51789
rs46492390	snp	C/G	0.35503	0.226867	intron-variant	Tnk2	Mm_Celera	16:32653208	AGTCTGCTTTCTTAC[C/G]GGTGATCTTAAAACA	51789
rs46505647	snp	A/G	0.152778	0.230321	intron-variant, nc-transcript-variant	Tnk2, Tnk2os	Mm_Celera	16:32666340	TTCCCTGTGCTCTCC[A/G]CTCTTCAGGTTCCTG	51789
rs46538266	snp	C/T			intron-variant	Tnk2	Mm_Celera	16:32655743	AGTGCCCACAGAGCC[C/T]GAAAGAGGGAGTGAT	51789
rs46607124	snp	C/T	0.336735	0.234472	intron-variant	Tnk2	Mm_Celera	16:32646227	CCCGTCTTTCAGCTT[C/T]ATCCCGTGCCAGTCA	51789
rs46713370	snp	C/T	0.142012	0.225474	downstream-variant-500B	Tnk2	Mm_Celera	16:32683841	TGAATTCAGAAGGTA[C/T]AGAGAGTACACAGCA	51789
rs46782428	snp	C/T	0.132653	0.220748	intron-variant	Tnk2, Tnk2os	Mm_Celera	16:32666794	TCCTTTCTAAAATTG[C/T]CATGTCTTTGGTAAA	51789
rs46953392	snp	A/G	0.260355	0.249785	intron-variant, upstream-variant-2KB	Tnk2	Mm_Celera	16:32657542	TCATGGCAGTATAGT[A/G]TTGGAGGTGAGCTGG	51789
rs46990874	snp	C/T	0.260355	0.249785	intron-variant	Tnk2	Mm_Celera	16:32654824	CTTCCATTCTTATGA[C/T]GCTTCTATTCCTGCT	51789
rs47114812	snp	C/T	0.152778	0.230321	intron-variant, utr-variant-5-prime	Tnk2	Mm_Celera	16:32673328	TCTTAGGAGTGGGCC[C/T]GTGTGCCTCTGGTTC	51789
rs47183994	snp	A/G	0.277778	0.248452	intron-variant	Tnk2	Mm_Celera	16:32676169	GTCCTCCAGCCCCGC[A/G]CATGCACACAGTTCT	51789
rs47246076	snp	A/G			intron-variant	Tnk2	Mm_Celera	16:32655828	AGGAATTGAACCTTC[A/G]TCTTTTGGAAGAGCA	51789
rs47321410	snp	C/T	0.142012	0.225474	synonymous-codon, upstream-variant-2KB	Tnk2, Tnk2os	Mm_Celera	16:32669962	CCTCAGGTGACAGAG[C/T]TGGCACCTCTGGGAT	51789
rs47341647	snp	A/G	0.132653	0.220748	intron-variant, upstream-variant-2KB	Tnk2, Tnk2os	Mm_Celera	16:32668545	TTCAGGTTTAACTGA[A/G]CACAGTGATTTCTTT	51789
rs47389037	snp	C/T	0.35503	0.226867	intron-variant	Tnk2	Mm_Celera	16:32652080	GTCTACAAGCTGATG[C/T]TGATTTTCGTGATGT	51789
rs47397133	snp	A/G			intron-variant	Tnk2	GRCm38.p3	16:32655923	TTGGCTCTTCCATGC[A/G]AGTTTTAAGTTTTTC	51789
rs47441963	snp	G/T	0.336735	0.234472	intron-variant	Tnk2	Mm_Celera	16:32673604	CGTCTGTAAGCTCAG[G/T]CTCAGGGTTTGGGGC	51789
rs47442094	snp	C/T	0.336735	0.234472	intron-variant	Tnk2	Mm_Celera	16:32676657	ATGAACTCATTCTGA[C/T]TTGTTAAAATGGCCC	51789
rs47537825	snp	C/T	0.142012	0.225474	intron-variant, upstream-variant-2KB	Tnk2, Tnk2os	Mm_Celera	16:32669895	CTGGGAACTTTGCCT[C/T]TGAGAGAGTGGCATC	51789
rs47570010	snp	A/G	0.142012	0.225474	intron-variant, upstream-variant-2KB	Tnk2	Mm_Celera	16:32670424	AAGGAATTCTCCAGG[A/G]ATACTGGAAGGCACA	51789
rs47630259	snp	C/T	0.260355	0.249785	intron-variant, nc-transcript-variant	Tnk2, Tnk2os	Mm_Celera	16:32666034	CTCAGGAGCCTTCTC[C/T]TGCTGCCCAGAGGTA	51789
rs47670018	snp	A/G	0.336735	0.234472	missense	Tnk2	Mm_Celera	16:32679597	CAGGCACCAAGGCAG[A/G]CCGCAGCAGTGGGGG	51789
rs47679098	snp	C/T	0.375	0.216506	intron-variant	Tnk2	Mm_Celera	16:32651441	GCTTGAGGGAGGAAA[C/T]GCTTGGAGAGATGGC	51789
rs47689876	snp	A/G			intron-variant, utr-variant-5-prime	Tnk2	Mm_Celera	16:32661480	AGCCCCCGTGACTTA[A/G]GGGCTTCAGTCGTGG	51789
rs47718335	snp	A/G	0.260355	0.249785	intron-variant	Tnk2	Mm_Celera	16:32664527	GTAGATGTATTTCCT[A/G]TGTCTCTTCTGTTTC	51789
rs47768821	snp	A/C	0.473373	0.11227	intron-variant, upstream-variant-2KB	Tnk2	GRCm38.p3	16:32659562	TGCTTTCGAAAAAGG[A/C]ACCGTATTCACAGGG	51789
rs47890994	snp	A/G	0.244898	0.249948	intron-variant, upstream-variant-2KB, utr-variant-5-prime	Tnk2	Mm_Celera	16:32672749	ATTGTTAGGTAAGAC[A/G]TGGAAGCAGGAAGGA	51789
rs47918007	snp	A/G	0.297521	0.245442	intron-variant, utr-variant-5-prime	Tnk2	Mm_Celera	16:32661234	GGGAGTAGGACCAGA[A/G]CTGTGAGCACTGCAC	51789
rs47986895	snp	C/T	0.277778	0.248452	intron-variant	Tnk2	Mm_Celera	16:32674213	GGGGCGGGCGTACTG[C/T]TCTGTGCGTCTCACG	51789
rs48018557	snp	A/G	0.375	0.216506	intron-variant	Tnk2	Mm_Celera	16:32662107	GGAGCAGGGAAGGGA[A/G]CTGAGCTGAGAGGTT	51789
rs48181436	snp	C/G	0.152778	0.230321	intron-variant	Tnk2	Mm_Celera	16:32662236	AGGATAAGACTCTGA[C/G]CTGTCACAGGAATGG	51789
rs48203389	snp	C/T	0.336735	0.234472	intron-variant	Tnk2	Mm_Celera	16:32676096	AAGGTGTTCCCATAG[C/T]ACATCTTGAAGCTTA	51789
rs48228731	snp	C/T	0.132653	0.220748	intron-variant	Tnk2	Mm_Celera	16:32670292	GTCTCAGCAGATCCA[C/T]ACCTCCAACTTCTGG	51789
rs48320558	snp	A/G	0.132653	0.220748	intron-variant, upstream-variant-2KB	Tnk2, Tnk2os	Mm_Celera	16:32669946	TCTGTCTTCTGTGTG[A/G]CCTCAGGTGACAGAG	51789
rs48374065	snp	G/T	0.132653	0.220748	utr-variant-3-prime	Tnk2	Mm_Celera	16:32683021	CTGGGCTGGTGGCTA[G/T]AGTGTGCCCCAGGCT	51789
rs48398339	snp	C/T	0.260355	0.249785	intron-variant	Tnk2	Mm_Celera	16:32677888	TGACCTGGTTCTCCC[C/T]AACAGACTGTACCTG	51789
rs48400609	snp	A/C	0.297521	0.245442	intron-variant	Tnk2	Mm_Celera	16:32655922	TTTGGCTCTTCCATG[A/C]AAGTTTTAAGTTTTT	51789
rs48460001	snp	C/T	0.336735	0.234472	intron-variant	Tnk2	Mm_Celera	16:32676436	GTCTCAGCTGCTTTG[C/T]TCCAGAAGCTCACCT	51789
rs48497774	snp	C/T	0.142012	0.225474	intron-variant	Tnk2	Mm_Celera	16:32650656	CAATGCAAAAATACC[C/T]TGGGCAGAAAGGTTT	51789
rs48549593	snp	A/G	0.35503	0.226867	intron-variant	Tnk2	Mm_Celera	16:32646366	AATTCTGCTCTCAGC[A/G]CATACATAAAGCATA	51789
rs48579485	snp	A/G	0.142012	0.225474	intron-variant	Tnk2	Mm_Celera	16:32678016	TCCTAGGTGTTCCCC[A/G]TTCACTGGCCACCCT	51789

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