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
rs8252879	snp	A/G	0.142012	0.225474	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7665786	AAAAAGGACCCTTAA[A/G]TTACCCTGGAAGTAT	69912
rs8252880	snp	A/C	0.124444	0.216185	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7665762	GAAGTATTTTCATTA[A/C]NGTACCAANTTAATA	69912
rs8252881	snp	A/G	0.488166	0.0760073	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7665761	AAGTATTTTCATTAA[A/G]GTACCAAATTAATAT	69912
rs8252882	snp	A/C	0.124444	0.216185	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7665753	TCATTANNGTACCAA[A/C]TTAATATCTTCCTCT	69912
rs8252883	snp	C/T	0.493827	0.0552116	upstream-variant-2KB, intron-variant	Pcmt1, Nup43	GRCm38.p3	10:7665572	AAGAGGGTCTAGGAT[C/T]CCCCCTGGAACTAGG	69912
rs8252884	snp	C/T	0.124444	0.216185	upstream-variant-2KB, intron-variant	Pcmt1, Nup43	GRCm38.p3	10:7665552	ctggaactagggtta[C/T]aaaggattgtcagcn	69912
rs8252885	snp	C/T	0.124444	0.216185	upstream-variant-2KB, intron-variant	Pcmt1, Nup43	GRCm38.p3	10:7665537	naaaggattgtcagc[C/T]accacgtgggtgctg	69912
rs29310987	snp	A/C	0.32	0.24	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7673898	TAGATTTACAGGCAA[A/C]TAGAATTGCCATGTG	69912
rs29313753	snp	A/G	0.375	0.216506	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667291	CTGCCTCTGCCTCCC[A/G]AGTTCTGGGATTAAA	69912
rs29314743	snp	C/T	0.5	0	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672582	GTAGCTGTCTTCAGA[C/T]ACACCAGAAGAGGGC	69912
rs29315027	snp	C/T	0.444444	0.157135	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666513	ATACATACATACATA[C/T]GAATAATTAAAATAC	69912
rs29315122	snp	C/T	0.375	0.216506	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667399	AAAGAACATCTCAAA[C/T]TCTTTCAGCCCAAGG	69912
rs29316890	snp	G/T	0.32	0.24	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7676973	TTCCTCCAGTCTCCA[G/T]GCACCAGGCACACAC	69912
rs29321290	snp	C/G	0.498615	0.0262793	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7665890	CTGAAAGTTTTTATA[C/G]GTTTATTTTATGCAT	69912
rs29321996	snp	A/G	0.444444	0.157135	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671914	CCCTAGACCTGTTGG[A/G]TCAGAATCTCCAGGT	69912
rs29322740	snp	C/T	0.32	0.24	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666039	TCCCGGTAATGTCTT[C/T]GCCTGCATGTATGTA	69912
rs29326464	snp	A/G	0.32	0.24	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677107	TGCATGTTTATATTC[A/G]TCAATGTGTATATAA	69912
rs29326578	snp	G/T	0.444444	0.157135	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671706	AGCCGGAAAGGGAAA[G/T]TGGGATGGATTGCAA	69912
rs29326622	snp	A/T	0.444444	0.157135	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7676196	GGGTAGGCCATAAAA[A/T]AACCTCTGTGGATTA	69912
rs29326656	snp	C/T	0.375	0.216506	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668202	CACCTTATAGTTTGT[C/T]TACCCTTACCCCTGA	69912
rs29328264	snp	A/G	0.5	0	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668401	GCAGGAGGGATCTCA[A/G]AGCTAGTCAGGGCTA	69912
rs29336403	snp	G/T	0.375	0.216506	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667295	CTCTGCCTCCCGAGT[G/T]CTGGGATTAAAGGCG	69912
rs29338571	snp	A/T	0.5	0	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672585	GCTGTCTTCAGACAC[A/T]CCAGAAGAGGGCGTC	69912
rs29341618	snp	A/G	0.375	0.216506	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666679	CTTACCACTAGGCAT[A/G]AACACACGCAGCACA	69912
rs29342042	snp	A/G	0.32	0.24	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668460	TAACAATATTTGTCC[A/G]TCTATGTGCCAAACG	69912
rs29343832	snp	C/T	0.375	0.216506	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671143	TCCTATTTCTTCTAT[C/T]CATTACATAGTAATT	69912
rs29345608	snp	C/T	0.444444	0.157135	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677877	TCAAATCTCAGCAAC[C/T]GCATGGTGGCTCACA	69912
rs29346083	snp	C/T	0.444444	0.157135	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671886	TTGCCTGAGAAGATT[C/T]CAGGCCCCCCCACCC	69912
rs29347471	snp	A/C	0.5	0	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7673755	TATTATGATAAAAAA[A/C]TTGTTTAATTAGTTA	69912
rs29349309	snp	A/T	0.375	0.216506	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666779	TTAAAAATAATTTTT[A/T]AAAAAATTAGTTATC	69912
rs29350767	snp	A/G	0.5	0	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668450	TTATCTTAAATAACA[A/G]TATTTGTCCGTCTAT	69912
rs29355827	snp	C/G	0.375	0.216506	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674441	TGTGTAATCTTTGCT[C/G]CTTTCTTAAGAAACT	69912
rs29356449	snp	A/G	0.444444	0.157135	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672214	GAACAACATAGTGAA[A/G]TCCTGGCTCAAAGCT	69912
rs29366440	snp	C/T	0.32	0.24	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677154	AGGCCACATCAGATC[C/T]CCTGAAGCTGGAGTT	69912
rs29366748	snp	A/G	0.375	0.216506	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7676698	AGGCCTAGAGAGAGT[A/G]TAGTCTCAGCAGTTG	69912
rs29367152	snp	C/G	0.444444	0.157135	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666528	TGAATAATTAAAATA[C/G]TAAGAAGAAAGCTGT	69912
rs29367930	snp	C/T	0.5	0	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672576	TACACTGTAGCTGTC[C/T]TCAGACACACCAGAA	69912
rs29370203	snp	C/T	0.444444	0.157135	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672288	TGAGGAAGCTGCTGA[C/T]GAAGGTAAAGATGGG	69912
rs29370497	snp	A/T	0.492188	0.0620098	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7666934	TAAAATCCAATATGG[A/T]GCTACACAGCTTCGG	69912
rs29373535	snp	C/T	0.375	0.216506	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7669399	TTTTCGATGTTAACA[C/T]ATTTTATTTGCTTTG	69912
rs29375513	snp	A/G	0.375	0.216506	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670386	CTTAGGCATACATAT[A/G]TGCACATAAATGTTT	69912
rs29379353	snp	A/G	0.444444	0.157135	missense, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7676329	TGGGATGCCTCCACA[A/G]ATGCACCTGAAAAGT	69912
rs33850652	snp	C/T	0.375	0.216506	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672768	ACCAAAATTTCTTAT[C/T]TGATCTAGGGGTTGT	69912
rs45702115	snp	A/T	0.132653	0.220748	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670130	CACTTAGCTTCTAAC[A/T]CAGATACCACAAAGA	69912
rs45710397	snp	A/G	0.444444	0.157135	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7673085	TAAGATTGGATAGAC[A/G]GGAGCTTGAACATCT	69912
rs45880139	snp	A/G	0.408163	0.193609	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7669906	CTGAGAATCTCAGAT[A/G]TAGTAAGCATGCATT	69912
rs46038273	snp	G/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666337	TTTCTCTGTCAGGGC[G/T]AGAGAGATGGCTCGC	69912
rs46065360	snp	C/G	0.124444	0.216185	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7665857	GCGGAACTACACACC[C/G]AGTCCTAGCTGAGGA	69912
rs46322892	snp	A/C	0.124444	0.216185	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7669708	GATTGTGTTAGTAAG[A/C]GCACAGTGCTTTATA	69912
rs46365313	snp	C/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667184	CTTTTTTGTTTTGTT[C/T]TTGTTTTTTCGAGAC	69912
rs46649681	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671479	CGGATTTCTGAGTTC[A/G]AGACCAGCCTGGTCT	69912
rs46726420	snp	A/G	0.497778	0.0332592	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667764	TTGCTGGTCTGGTTT[A/G]GCTGCCCGCTACTTG	69912
rs47362962	snp	A/G	0.231111	0.249285	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671819	TGACTGACACCAGTC[A/G]TGATTTGGCCAGTGT	69912
rs47824970	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668875	GCTGGGCGGGGTGGC[A/G]CAGGCCTTTAATCCC	69912
rs48019057	snp	G/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666197	AGGGTTTTTAAAGTG[G/T]TTTTTTTTTGTTTTT	69912
rs48120410	snp	A/G	0.142012	0.225474	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667819	CTGGGATCTGGTTTT[A/G]AACCCTCACCAAGTC	69912
rs48339507	snp	C/T	0.486111	0.0821678	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671656	TTTACTGTGAGCTGG[C/T]CTTAGATATTTGTTA	69912
rs48489442	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674421	TTTTTCCAGAGCTTT[C/T]TAGATGTGTAATCTT	69912
rs48937784	snp	A/C			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668843	AAGCACACCCCAATC[A/C]AAAAAAAAAAAATCG	69912
rs49082004	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675640	GATTACAGGCATGAG[C/T]CACCACTCTTTGATA	69912
rs49346059	snp	A/G	0.277778	0.248452	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671662	GTGAGCTGGCCTTAG[A/G]TATTTGTTACTGGAG	69912
rs49897027	snp	C/G/T			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7668866	AAAAATCGTGCTGGG[C/G/T]GGGGTGGCGCAGGCC	69912
rs50913545	snp	C/T	0.124444	0.216185	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670125	GTTCACACTTAGCTT[C/T]TAACTCAGATACCAC	69912
rs51198283	snp	A/G	0.408163	0.193609	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667772	CTGGTTTAGCTGCCC[A/G]CTACTTGAGAGCCCT	69912
rs51745260	snp	C/G/T			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7668986	ATACAGTGAAACCCT[C/G/T]TCTCAAAAAACCAAA	69912
rs51833866	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677721	TGATTCCTACAGGAC[A/G]CCTTCTGACCTCCAC	69912
rs51878318	snp	C/T	0.124444	0.216185	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670061	CTTTGTGAGCTCCTC[C/T]GATAGTCTTTTGGAG	69912
rs51913429	snp	C/T	0.32	0.24	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7669336	GTAAAATTTTAAGCT[C/T]ACTCTTTATCTTTCA	69912
rs52377955	snp	A/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677983	AAATAAATAATCTTT[A/T]AAAAATATATAAGAT	69912
rs52629299	snp	A/G	0.124444	0.216185	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7665844	CTATAATTTTAATGC[A/G]GAACTACACACCCAG	69912
rs107657219	snp	G/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666221	TGTTTTTGTTTTTTT[G/T]TTTTTTTTTTTTTTT	69912
rs211889239	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7669730	TGCTTTATAGTGTTG[A/G]AACATGAGGAGAGGC	69912
rs211948056	snp	A/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677674	TGACAACGGAGTTTG[A/T]TTGGCAGGACTCAAG	69912
rs211993301	snp	A/C			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7678215	TTAGTGGTACAGAGT[A/C]AGCCTTGTGGTTTGA	69912
rs212263680	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670571	CATGTAAAAAAGATA[C/T]AGAGGTTAGTTCCTT	69912
rs212451693	snp	C/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675903	AGAAAGGTGTGATCC[C/G]AGCAGCTAGGTCACA	69912
rs212503128	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677121	CGTCAATGTGTATAT[A/G]AGTGTAGTTGGCAGC	69912
rs212640578	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668340	TGAATTGCCCAAACC[A/G]GGCATGGTGGTACAA	69912
rs212707986	snp	C/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667316	ATTAAAGGCGTGCGC[C/T]ACCACGCCGGGCAGA	69912
rs212875429	snp	A/C/G			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7675348	TATTACTACATGCTC[A/C/G]TCTTACTGAGCTGAT	69912
rs213101668	snp	A/C			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7673567	AGGAACCTGTTAACG[A/C]ATTTTTAAAACTTGC	69912
rs213279983	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674574	TAGACTATGTATTGG[C/T]GTGGCTTAGCTATGT	69912
rs213290641	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668408	GGATCTCAAAGCTAG[C/T]CAGGGCTACATATAC	69912
rs213358326	snp	A/C			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7676885	GCTCCTCTAAAGGAC[A/C]CTGTTTCAATTCACA	69912
rs213632690	snp	G/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666225	TTTGTTTTTTTTTTT[G/T]TTTTTTTTTTTTTAT	69912
rs213840176	snp	G/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667378	TTGTTCAGAGCTGCC[G/T]ACATGAAAGAACATC	69912
rs214021954	in-del	-/CT			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7676794	GGGCTACATGAGACC[-/CT]GTTTCCAAAAAACAA	69912
rs214092428	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675268	CTGGCCCGTATAAGC[C/T]AGATAATCTCTTCCT	69912
rs214216043	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7676006	GAGAATCTTATTCCT[A/G]TGCAGATGAGCTGGG	69912
rs214507585	in-del	-/AAG			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671559	AAAAAAAAAAGAAAA[-/AAG]AAAGACAGACAGACA	69912
rs214548640	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674654	ACTGGGCTGACATAC[A/G]ACTGGGAGCCACTGA	69912
rs214877844	snp	C/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674702	GGGTCCTCTGGAACA[C/G]TATCTGCCCAGAACT	69912
rs215008147	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675309	CCTTTAATGTTCGTT[C/T]ATCATATCTACAACT	69912
rs215184904	snp	C/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672687	AGTCTGTGCTCTTAA[C/G]CACTGAGCCCTCAAG	69912
rs215188603	in-del	-/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668662	TCAGATGGATGGACA[-/G]GGGTCTTTTGAACAT	69912
rs215281150	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7673426	TCTCTGTGTACCCCT[A/G]GGTGTCCTGGAACTC	69912
rs215357094	in-del	-/GAAAGACAGAC			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7671561	AAAAAAAAGAAAAAA[-/GAAAGACAGAC]AGACAGACAGACAGA	69912
rs215557938	snp	G/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672761	TCCGCATACCAAAAT[G/T]TCTTATTTGATCTAG	69912
rs215972543	in-del	-/C			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670510	CCACCTGCATTTGCT[-/C]CCCAATGTCACCGTG	69912
rs216125678	snp	A/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7678320	TAGGAGGTGTGGCCT[A/T]GTGGGAAGGGGTGGG	69912

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