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
rs4229226	snp	C/T	0.21875	0.248039	synonymous-codon, intron-variant, downstream-variant-500B	Itsn2, Fam228a	Mm_Celera	12:4713128	CCGACTACTACTGCA[C/T]GAAGTCCCCACTGGA	20403
rs4229227	snp	A/G	0.21875	0.248039	utr-variant-3-prime, intron-variant, downstream-variant-500B	Itsn2, Fam228a	Mm_Celera	12:4713206	CCTTTGAGGGCCTGG[A/G]GAAGCCAGAACCAGG	20403
rs4229228	snp	C/T	0.21875	0.248039	utr-variant-3-prime, intron-variant, downstream-variant-500B	Itsn2, Fam228a	Mm_Celera	12:4713229	GAACCAGGGGAGCTG[C/T]CCACAAGGCTGGGTC	20403
rs4229229	snp	C/G	0.21875	0.248039	utr-variant-3-prime, intron-variant, downstream-variant-500B	Itsn2, Fam228a	Mm_Celera	12:4713251	GGCTGGGTCTAAAGA[C/G]AGATTTTGCTCTCCC	20403
rs4229230	snp	C/T	0.21875	0.248039	utr-variant-3-prime, downstream-variant-500B, intron-variant	Itsn2, Fam228a	Mm_Celera	12:4713381	GATCTTTTAAACAAA[C/T]GCCACAGCACAGTGC	20403
rs4229231	snp	A/G	0.265928	0.249492	utr-variant-3-prime, downstream-variant-500B, intron-variant	Itsn2, Fam228a	GRCm38.p3	12:4713437	CTGTGTTAGATGCCA[A/G]GGTTTCCATTTTCAG	20403
rs4229232	snp	A/G	0.30839	0.243086	utr-variant-3-prime, downstream-variant-500B, intron-variant	Itsn2, Fam228a	Mm_Celera	12:4713511	ACGTTACCACTTGGC[A/G]AATCTGTCCACTGTG	20403
rs4229233	snp	A/G	0.21875	0.248039	utr-variant-3-prime, downstream-variant-500B, intron-variant	Itsn2, Fam228a	Mm_Celera	12:4713547	GGTGATGTTGGAACC[A/G]TTCCACACTATGTGA	20403
rs6197893	snp	C/T	0.5	0	intron-variant	Itsn2	Mm_Celera	12:4648138	AAGCTACTGCAGCTC[C/T]CAGTCTTAAAGAATA	20403
rs6197935	snp	A/G	0.5	0	intron-variant	Itsn2	Mm_Celera	12:4648176	GGCTAATGTTACACA[A/G]ATTAAGATCATNCAT	20403
rs6197964	snp	A/G	0.5	0	intron-variant	Itsn2	Mm_Celera	12:4648188	ACANATTAAGATCAT[A/G]CATTAATTTGGATTC	20403
rs6245947	snp	C/T	0.5	0	intron-variant	Itsn2	Mm_Celera	12:4663274	ctagacatgggtatg[C/T]atgcttgtagattca	20403
rs6246581	snp	A/G	0.345679	0.230967	intron-variant	Itsn2	GRCm38.p3	12:4663404	AGCCTGGAGACATTA[A/G]CATTAAACAAGGCTG	20403
rs6247024	snp	A/G	0.5	0	intron-variant	Itsn2	Mm_Celera	12:4663452	GCTCTCTTCTATGCT[A/G]CTCACAGTTCAGTCA	20403
rs6247078	snp	G/T	0.48	0.0979796	intron-variant	Itsn2	GRCm38.p3	12:4663471	ACAGTTCAGTCACGG[G/T]TCCTGNGACTCCTCT	20403
rs6247098	snp	A/G	0.5	0	intron-variant	Itsn2	Mm_Celera	12:4663477	CAGTCACGGNTCCTG[A/G]GACTCCTCTGTATCC	20403
rs6247491	snp	C/T	0.5	0	intron-variant	Itsn2	Mm_Celera	12:4656945	ttgtatctctagttg[C/T]atatgtagcagagga	20403
rs6247555	snp	A/C	0.5	0	intron-variant	Itsn2	Mm_Celera	12:4663542	AACTTTTAAAACTAG[A/C]ATCTTGGAGTAACAT	20403
rs6247556	snp	A/G	0.5	0	intron-variant	Itsn2	Mm_Celera	12:4656982	agtcagccatcaatg[A/G]gaggagacacccttg	20403
rs6247973	snp	C/T	0.5	0	intron-variant	Itsn2	Mm_Celera	12:4657033	GGCAAGATAACCAAG[C/T]ATAAACTTGGAGGTG	20403
rs6248011	snp	C/T	0.231111	0.249285	intron-variant	Itsn2	Mm_Celera	12:4657050	TAAACTTGGAGGTGC[C/T]GTCACTGTTTAAGGC	20403
rs6280460	snp	A/G	0.484429	0.0868505	intron-variant	Itsn2	GRCm38.p3	12:4691862	AATAGTGTTTAACCC[A/G]GTGTATTCAAAATAC	20403
rs6280514	snp	C/T	0.415225	0.187619	intron-variant	Itsn2	Mm_Celera	12:4691893	CATACCAATATATAA[C/T]GAGTTTGGTTGCTCA	20403
rs6281549	snp	A/G	0.5	0	intron-variant	Itsn2	Mm_Celera	12:4692050	ggcCAAtattgatag[A/G]atggtttacagttca	20403
rs6281624	snp	G/T	0.5	0	intron-variant	Itsn2	Mm_Celera	12:4692101	acccagtgtgtggtt[G/T]gcatctgcagcacat	20403
rs6282774	snp	C/T	0.5	0	intron-variant	Itsn2	Mm_Celera	12:4665484	TCACATGAGGCCGTT[C/T]AGTAACAAANACTCA	20403
rs6282790	snp	A/G	0.444444	0.157135	intron-variant	Itsn2	GRCm38.p3	12:4665494	CCGTTNAGTAACAAA[A/G]ACTCATTTGTCATCT	20403
rs6284446	snp	C/T	0.5	0	intron-variant	Itsn2	GRCm38.p3	12:4665794	AAGCAGTGAGGCCTC[C/T]GCCAGCCACAGCTGC	20403
rs6297773	snp	C/T	0.5	0	intron-variant	Itsn2	Mm_Celera	12:4665908	CTGCAGCATAAGCAA[C/T]CATCTCTCCTTTCTT	20403
rs29122616	snp	A/G	0.5	0	intron-variant	Itsn2	Mm_Celera	12:4619286	CTCTGTTAGTACTAT[A/G]TCCAATTTTCTGAGG	20403
rs29216353	snp	C/T	0.444444	0.157135	intron-variant	Itsn2	Mm_Celera	12:4600710	CCCAGCCCCACTCTT[C/T]TTGACACATTCCTAG	20403
rs29223400	snp	C/T	0.444444	0.157135	intron-variant	Itsn2	Mm_Celera	12:4600707	CCCCCCAGCCCCACT[C/T]TTCTTGACACATTCC	20403
rs45634673	snp	A/G	0.132653	0.220748	intron-variant	Itsn2	Mm_Celera	12:4683385	GGCGAATCCAGGTTG[A/G]CCAAGTTACATTCAG	20403
rs45635489	snp	C/T	0.124444	0.216185	intron-variant	Itsn2	Mm_Celera	12:4648481	ACAACCCATAACCAC[C/T]GTCCTCTTTTGTTTC	20403
rs45661688	snp	C/G	0.124444	0.216185	intron-variant	Itsn2, Fam228a	Mm_Celera	12:4705983	TGACAGAACTCCACA[C/G]AGTGACTGCTTCCTG	20403
rs45662344	snp	G/T	0.32	0.24	intron-variant	Itsn2	GRCm38.p3	12:4689923	ACTCCCGAAGCCTGC[G/T]CGCTCATTCACCGCC	20403
rs45668975	snp	A/T	0.231111	0.249285	intron-variant	Itsn2	Mm_Celera	12:4611812	ACTTTCAGACATACA[A/T]CTTATTTTTCTTTTA	20403
rs45703356	snp	G/T	0.277778	0.248452	intron-variant	Itsn2	Mm_Celera	12:4594880	CCACTAAACTTCCTT[G/T]AGTATCACAGTGTAT	20403
rs45706248	snp	C/T	0.260355	0.249785	intron-variant	Itsn2	Mm_Celera	12:4595550	CGGACAATCAGGGAG[C/T]TACTACCAGATGGGA	20403
rs45723939	snp	A/C	0.124444	0.216185	intron-variant	Itsn2, Fam228a	Mm_Celera	12:4706032	TTGACCTGGGGCAGC[A/C]GCTACATTGAGAGAA	20403
rs45726201	snp	A/T	0.21875	0.248039	intron-variant	Itsn2, Fam228a	Mm_Celera	12:4712151	CTATGGATTGGGCCA[A/T]TATCATTCACAGTTT	20403
rs45759685	snp	C/T	0.231111	0.249285	intron-variant	Itsn2	Mm_Celera	12:4692292	ATTTTGGCAGCTCTG[C/T]GTGCCTCTGATTGAC	20403
rs45765240	snp	C/T	0.142012	0.225474	intron-variant	Itsn2	Mm_Celera	12:4642002	AGGCGATTGAGAACA[C/T]TAAAGGGGTGTGAGA	20403
rs45784477	snp	C/G/T	0.336735	0.234472	intron-variant	Itsn2	Mm_Celera	12:4652852	GTCCAATCTAACATA[C/G/T]TTCTGTAGTGCATCT	20403
rs45790153	snp	C/T	0.32	0.24	intron-variant	Itsn2, Fam228a	Mm_Celera	12:4701156	GACATTTGTGGAGAA[C/T]GGATGTGACTGCCAG	20403
rs45793876	snp	C/T	0.32	0.24	intron-variant	Itsn2	Mm_Celera	12:4662923	GATTGGCCTGGAGTC[C/T]GGAAGGATGAAGTAG	20403
rs45801880	snp	A/C	0.244898	0.249948	intron-variant	Itsn2	Mm_Celera	12:4642355	TCACAGGCTCTGCTT[A/C]CATGTTCACCATGCA	20403
rs45805572	snp	C/T	0.391111	0.206368	intron-variant	Itsn2	Mm_Celera	12:4696366	ATGAGGAGGGATTTC[C/T]CAGGGTAGTTCCCAG	20403
rs45809024	snp	A/G			intron-variant	Itsn2	Mm_Celera	12:4605607	AATGTTTATTGTTGG[A/G]CTGGAGAGGTGCCTC	20403
rs45812608	snp	G/T			intron-variant	Itsn2	Mm_Celera	12:4660560	AGCACCTACGTCAGG[G/T]GGCTCACACCTTCCT	20403
rs45824883	snp	C/T	0.124444	0.216185	intron-variant	Itsn2, Fam228a	Mm_Celera	12:4699744	CTTTTTCTGCAGGCT[C/T]CACTGTGCAGAGCCC	20403
rs45839110	snp	A/G	0.152778	0.230321	intron-variant	Itsn2	Mm_Celera	12:4598639	CTTGTGTTCATGATG[A/G]TGAGCATTTCCCCAG	20403
rs45843224	snp	G/T	0.426035	0.177515	intron-variant	Itsn2	Mm_Celera	12:4597226	ACTCTTGCATCTCTC[G/T]CAGATCGCCTCTTCA	20403
rs45850233	snp	C/G	0.5	0	intron-variant	Itsn2	Mm_Celera	12:4662655	CTGCAGGAGTGTCAG[C/G]TGGCCAGATGGCTTT	20403
rs45857558	snp	C/T	0.444444	0.157135	intron-variant	Itsn2, Fam228a	GRCm38.p3	12:4708290	CAGCACAGGCTTGTC[C/T]CAGTGCCATAAGTCC	20403
rs45859311	snp	C/T	0.152778	0.230321	synonymous-codon, intron-variant	Itsn2	Mm_Celera	12:4640936	TATGGATGACTGTGT[C/T]CTTCAGTGCCTTTTG	20403
rs45860314	snp	A/T	0.32	0.24	intron-variant	Itsn2	Mm_Celera	12:4684246	GTTAAGTCTGTGTTA[A/T]GCCGACAGGGGCAGG	20403
rs45860448	snp	C/T			intron-variant	Itsn2	Mm_Celera	12:4659206	CGCAAAGAGACTTGT[C/T]TGCACAATGTTGAGG	20403
rs45876321	snp	A/G	0.46875	0.121031	intron-variant	Itsn2	Mm_Celera	12:4666001	AGACAGTTGTTAACC[A/G]ATGGCTTCTATTCCA	20403
rs45929327	snp	C/T	0.48	0.0979796	intron-variant	Itsn2	GRCm38.p3	12:4694818	TCCACACTTCATTGT[C/T]GTCTTCTAGATCAGC	20403
rs45933119	snp	C/T			intron-variant	Itsn2	Mm_Celera	12:4667160	AGGAAGAAGTCAAAA[C/T]ATCACTATTTGCAGA	20403
rs45949609	snp	C/T	0.32	0.24	intron-variant	Itsn2	Mm_Celera	12:4686871	AGAGAACGAACGTAT[C/T]TTTACACACAGAGTA	20403
rs45959567	snp	G/T	0.444444	0.157135	intron-variant	Itsn2, Fam228a	Mm_Celera	12:4710960	AAGGCTTACATAGAA[G/T]TGAAATGTTGATGAG	20403
rs45977285	snp	A/G	0.489796	0.070696	intron-variant, downstream-variant-500B	Itsn2, Fam228a	GRCm38.p3	12:4712872	TCCAGATAGGCAGCC[A/G]TCACTGGGCATCTGC	20403
rs45999972	snp	A/C	0.244898	0.249948	intron-variant	Itsn2	Mm_Celera	12:4692960	GTAAAGGGCAGCGGT[A/C]AAAGGGTTGGAACCT	20403
rs46017515	snp	C/T	0.444444	0.157135	intron-variant	Itsn2	Mm_Celera	12:4662072	CGAGGAGAGTAAGCA[C/T]CCCGTGTTCTTATGT	20403
rs46036357	snp	A/C	0.391111	0.206368	intron-variant	Itsn2	Mm_Celera	12:4609130	TTAACTTTTTCAGCA[A/C]ATATTTAAAAGTACT	20403
rs46039548	snp	A/C	0.142012	0.225474	intron-variant	Itsn2	Mm_Celera	12:4639971	CTATTTTGTCATGAG[A/C]CGAGATATTTTCCCT	20403
rs46060457	snp	A/G	0.444444	0.157135	intron-variant	Itsn2	GRCm38.p3	12:4687195	AGGAAGCTGCCTGTC[A/G]TTTTGCCCTTTCTTC	20403
rs46076982	snp	A/G	0.152778	0.230321	intron-variant	Itsn2	Mm_Celera	12:4625137	TACTTTATTTTTCCC[A/G]CAACTGTCTTAATTT	20403
rs46082144	snp	A/T	0.152778	0.230321	intron-variant	Itsn2	Mm_Celera	12:4624745	ATAGAATTCTACTTT[A/T]TGTCCTTCAAACATT	20403
rs46090417	snp	C/T	0.231111	0.249285	intron-variant	Itsn2, Fam228a	Mm_Celera	12:4699849	GCCCTTAAAAATCAG[C/T]CTTAATTGAGTTTTA	20403
rs46100169	snp	A/G	0.32	0.24	intron-variant	Itsn2	Mm_Celera	12:4690516	ACACACATGTTTGGA[A/G]AAAAGTAAAGGCAGA	20403
rs46155659	snp	C/G	0.244898	0.249948	intron-variant	Itsn2	Mm_Celera	12:4662432	TCTTTTAGTTACTGA[C/G]TTTTTTGACCCATAT	20403
rs46194275	snp	A/G	0.35503	0.226867	intron-variant, utr-variant-3-prime	Itsn2	Mm_Celera	12:4678549	TCAGCATCTGCAATC[A/G]GTCTGAAAATATGTT	20403
rs46211108	snp	A/G	0.142012	0.225474	intron-variant	Itsn2	Mm_Celera	12:4595379	AACTCTAAGAGTGCA[A/G]CGTATTTCATTTGCA	20403
rs46231036	snp	A/G			intron-variant	Itsn2	Mm_Celera	12:4627196	TCTAGAATATCTGGG[A/G]TCATGTTTTTTAAAA	20403
rs46244388	snp	C/T	0.345679	0.230967	synonymous-codon, intron-variant	Itsn2, Fam228a	Mm_Celera	12:4712594	GGATCTTTACCAGGA[C/T]GTTCTGTGTCTCACT	20403
rs46293303	snp	C/G	0.277778	0.248452	intron-variant	Itsn2	Mm_Celera	12:4603667	GTATGTCTTACTGAA[C/G]ACTGATTTTTTAAAA	20403
rs46312098	snp	A/G	0.231111	0.249285	intron-variant	Itsn2, Fam228a	Mm_Celera	12:4698697	TGGAGCTGAGACATC[A/G]CCACAGTTCACAGAG	20403
rs46330045	snp	A/G	0.142012	0.225474	intron-variant	Itsn2	Mm_Celera	12:4660184	TAATGAAAGTACATG[A/G]AGAGGAAGCTAGATT	20403
rs46337411	snp	A/T			intron-variant	Itsn2	Mm_Celera	12:4627208	GGGGTCATGTTTTTT[A/T]AAAATGTATTACAGT	20403
rs46356451	snp	G/T	0.32	0.24	intron-variant	Itsn2	Mm_Celera	12:4685364	CACTTTCTGATAGAA[G/T]CATACTACTTGATAT	20403
rs46359117	snp	C/T	0.32	0.24	intron-variant	Itsn2	Mm_Celera	12:4612245	CACCTGTCTGCCACA[C/T]TCAAGATTTATAACT	20403
rs46396007	snp	C/T	0.142012	0.225474	intron-variant	Itsn2	Mm_Celera	12:4642208	AGGCATGAAGACTAT[C/T]GGCTGCTCCTGAGGC	20403
rs46407228	snp	A/G	0.231111	0.249285	intron-variant	Itsn2, Fam228a	Mm_Celera	12:4698010	TCCACTGGGAACGCC[A/G]TCCTCCTCACGCCTG	20403
rs46430221	snp	G/T	0.32	0.24	intron-variant	Itsn2	Mm_Celera	12:4608724	GCAGAATGGTTGATA[G/T]CCATATTCCTAAGGC	20403
rs46446437	snp	G/T	0.124444	0.216185	intron-variant	Itsn2	Mm_Celera	12:4611991	TAATTCTGAGAGCCA[G/T]TTTTTGTTCTTTTTA	20403
rs46448303	snp	A/G	0.391111	0.206368	synonymous-codon, intron-variant	Itsn2, Fam228a	GRCm38.p3	12:4706343	GATCACTCGCTACCC[A/G]CTGCTCATCCGAAGT	20403
rs46464852	snp	A/G	0.32	0.24	intron-variant	Itsn2	Mm_Celera	12:4694176	AGCTGCCTGCCACCA[A/G]ACCACGCCCAAACTC	20403
rs46493927	snp	A/G	0.142012	0.225474	intron-variant	Itsn2	Mm_Celera	12:4600421	GTAGTGGGGAAAACA[A/G]CAGAAGGCCAGAGAC	20403
rs46494931	snp	A/T	0.231111	0.249285	intron-variant	Itsn2	Mm_Celera	12:4687026	GGAGTTAGGACTATT[A/T]GAGGAGAGGTGCTGA	20403
rs46497000	snp	A/G			intron-variant	Itsn2	Mm_Celera	12:4667153	ATTGGAAAGGAAGAA[A/G]TCAAAATATCACTAT	20403
rs46504049	snp	A/C	0.231111	0.249285	intron-variant	Itsn2	Mm_Celera	12:4686742	GTGGGGAGTAAGACC[A/C]AAAGTTCTTAGCACG	20403
rs46511402	snp	A/G	0.132653	0.220748	intron-variant	Itsn2, Fam228a	Mm_Celera	12:4700120	TCTGCACTGTGGCAT[A/G]CATGCCCCCGTCTTT	20403
rs46549211	snp	A/G	0.391111	0.206368	intron-variant	Itsn2	Mm_Celera	12:4610258	AAGCTGCCCATCGTT[A/G]CACATTATCCTCTTC	20403
rs46578829	snp	A/G	0.459184	0.136902	intron-variant	Itsn2, Fam228a	GRCm38.p3	12:4699381	GGTTTGCAGCTCATC[A/G]CTTGGCTAGTATGAC	20403
rs46604446	snp	C/T	0.260355	0.249785	intron-variant, upstream-variant-2KB	Itsn2, LOC105245369	Mm_Celera	12:4594480	AATGTTCAACATATC[C/T]AAAGGCTCAAATCCC	20403
rs46612905	snp	A/C	0.152778	0.230321	intron-variant	Itsn2	Mm_Celera	12:4626323	TGTTTAGGGTGAAGA[A/C]TCAAAGATGAGTAGC	20403
rs46634878	snp	C/T	0.152778	0.230321	intron-variant	Itsn2	Mm_Celera	12:4623874	GGCACTCTTTATTGT[C/T]CCCTTGTTCCTTCTT	20403

Full records

It may take some time, please wait.