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
rs3662659	snp	A/G	0.489796	0.070696	intron-variant	Amph	Mm_Celera	13:19048994	TGTGAAAATGTAACG[A/G]TACTTTATAACGATG	218038
rs3677044	snp	G/T	0.5	0	intron-variant	Amph	Mm_Celera	13:19049114	ATATAATAAATTTAT[G/T]GCACATTTTCTTAGT	218038
rs3677588	snp	A/G	0.5	0	intron-variant	Amph	Mm_Celera	13:19049163	AAAGAGTTCTTTGCA[A/G]CCTCTATCACAGAGT	218038
rs3677592	snp	C/T	0.5	0	intron-variant	Amph	Mm_Celera	13:19049167	AGTTCTTTGCAACCT[C/T]TATCACAGAGTGTAG	218038
rs3691273	snp	A/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19108103	CCTTCGAATAGAGTC[A/G]TTGATACAGCCAGTG	218038
rs3706716	snp	A/G	0.5	0	intron-variant	Amph	Mm_Celera	13:19108321	TACTGTTTTCTTGCG[A/G]TCACTTCTGGAGTTT	218038
rs4136930	snp	C/G	0.5	0	intron-variant	Amph	Mm_Celera	13:19049204	TATGCATTGTTCTCT[C/G]TGTATTAAAGGCAGA	218038
rs6153182	snp	C/T	0.5	0	intron-variant	Amph	Mm_Celera	13:19044834	GAACTGGAGCTGAGC[C/T]CCCCACAGGCGTTAA	218038
rs6153704	snp	A/G	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19044931	ATGCCACAGGATGTC[A/G]TAAGGCANATTTCTA	218038
rs6153717	snp	A/G	0.5	0	intron-variant	Amph	Mm_Celera	13:19044939	GGATGTCNTAAGGCA[A/G]ATTTCTAGAAGGCAA	218038
rs6153847	snp	A/G	0.32	0.24	intron-variant	Amph	Mm_Celera	13:19045020	ATATTAGGACACTTC[A/G]ACATCAACTACCAAA	218038
rs6166953	snp	C/T	0.5	0	intron-variant	Amph	Mm_Celera	13:19045086	TCAGATGGCTTCTTA[C/T]TTGTCTTCTNAAAAT	218038
rs6166971	snp	A/C	0.5	0	intron-variant	Amph	Mm_Celera	13:19045096	TCTTANTTGTCTTCT[A/C]AAAATGCTTCCTTTG	218038
rs6167514	snp	C/T	0.415225	0.187619	intron-variant	Amph	Mm_Celera	13:19045197	AAAAACTCTACTACA[C/T]TTCTGTCCATTGGAG	218038
rs6168069	snp	C/T	0.415225	0.187619	intron-variant	Amph	Mm_Celera	13:19045307	TATAACATCCTTGCA[C/T]TGCATATAATACAGT	218038
rs6168598	snp	A/G	0.5	0	intron-variant	Amph	Mm_Celera	13:19045364	TTATGAATTCTACTA[A/G]ACTGTCAGATGTTTT	218038
rs6289293	snp	C/T	0.5	0	intron-variant	Amph	Mm_Celera	13:19102624	TTTACATATCTAAAG[C/T]GGGGTCAATATTGCA	218038
rs6289882	snp	A/C	0.32	0.24	intron-variant	Amph	Mm_Celera	13:19102739	CTATTACTAACAACT[A/C]GNATTAAGCTGGACG	218038
rs6289884	snp	A/T	0.5	0	intron-variant	Amph	Mm_Celera	13:19102741	ATTACTAACAACTNG[A/T]ATTAAGCTGGACGTG	218038
rs6289933	snp	A/G	0.484429	0.0868505	intron-variant	Amph	Mm_Celera	13:19102768	CGTGGGGGATGAAAT[A/G]ACAGTGACATTAAGC	218038
rs6289977	snp	C/T	0.5	0	intron-variant	Amph	Mm_Celera	13:19102801	CAGGATGCCTCTGGG[C/T]TAAAGAANCTTGNGT	218038
rs6289991	snp	C/T	0.244898	0.249948	intron-variant	Amph	Mm_Celera	13:19102809	CTCTGGGNTAAAGAA[C/T]CTTGNGTTTTAGGAA	218038
rs6290388	snp	A/G	0.5	0	intron-variant	Amph	Mm_Celera	13:19102814	GGNTAAAGAANCTTG[A/G]GTTTTAGGAACCCTG	218038
rs6291498	snp	A/G	0.5	0	intron-variant	Amph	GRCm38.p3	13:19103038	TACCGGGGGTGTGGG[A/G]AAACTCATGGGAGGT	218038
rs6328590	snp	C/T	0.5	0	intron-variant	Amph	GRCm38.p3	13:19132091	TTACTCGAACAGTCC[C/T]GCGCTTCCATGCATA	218038
rs6328634	snp	A/G	0.493827	0.0552116	intron-variant	Amph	GRCm38.p3	13:19132109	GCTTCCATGCATACT[A/G]NAACATCACCTCCAA	218038
rs6328635	snp	C/T	0.5	0	intron-variant	Amph	GRCm38.p3	13:19132110	CTTCCATGCATACTN[C/T]AACATCACCTCCAAG	218038
rs13481715	snp	C/T	0.393491	0.20472	missense	Amph	GRCm38.p3	13:19139173	TCTCTACCCACCAGG[C/T]CATCCCTTCTGTTGT	218038
rs29224605	snp	A/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19103402	ATCTACAAAGTTCCA[A/T]TTATTCTACATTCCT	218038
rs29224801	snp	A/G	0.375	0.216506	missense	Amph	GRCm38.p3	13:19139370	GCATCTGCAGGTGCT[A/G]TGGATGCCTCGCTGT	218038
rs29224802	snp	A/C	0.444444	0.157135	intron-variant	Amph	GRCm38.p3	13:19114655	GGGTCCTCCTTAACT[A/C]ATGATCTCTGCAGTG	218038
rs29225257	snp	A/G	0.5	0	intron-variant	Amph	Mm_Celera	13:19077161	GACTAGCACCTTTAT[A/G]AGTACCGAGATGGAT	218038
rs29225595	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19053078	GTTGAAGAGTCAAGA[C/T]AGGGGAGAATTAACA	218038
rs29226659	snp	A/G	0.444444	0.157135	intron-variant	Amph	GRCm38.p3	13:19134176	AGCCCACATAGAGAC[A/G]TATAGGAAATGATCA	218038
rs29226918	snp	A/G	0.5	0	intron-variant	Amph	GRCm38.p3	13:19138849	CTCCTGTTGCCCTGC[A/G]GCAATCAAAGTCAGT	218038
rs29227502	snp	A/G	0.487535	0.077957	intron-variant	Amph	GRCm38.p3	13:19103385	TGAATAAGAAAAAGC[A/G]TATCTACAAAGTTCC	218038
rs29227505	snp	A/C	0.408163	0.193609	intron-variant	Amph	GRCm38.p3	13:19138021	CAAAGTTTAAGATTC[A/C]GCACTGTGTTTATAT	218038
rs29227921	snp	C/G	0.375	0.216506	intron-variant	Amph	GRCm38.p3	13:19137968	GGCTGGAAATGAAAA[C/G]GGACAGGGTAAGCCA	218038
rs29228135	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19069290	AAGTGTTTAATTTTA[C/T]CTCTGATTTTTTGTT	218038
rs29229489	snp	C/T	0.5	0	intron-variant	Amph	GRCm38.p3	13:19139092	AGAGAAAGTGGGTGG[C/T]TGGGAGAAGACACTG	218038
rs29231183	snp	A/C/T	0.375	0.216506	intron-variant	Amph	GRCm38.p3	13:19140204	GGCAGGTCCTCACCG[A/C/T]GTGACCTTCTGCTTT	218038
rs29232935	snp	A/G	0.497778	0.0332592	intron-variant	Amph	Mm_Celera	13:19096107	GGTAACCATGTTTCT[A/G]CTCCAGTTTGCACCC	218038
rs29233957	snp	C/T	0.415225	0.187619	intron-variant	Amph	GRCm38.p3	13:19114677	TCTGCAGTGCTCACA[C/T]AAGCTCTCAGAGCCT	218038
rs29233977	snp	A/G	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:19106679	CCTTAACTATAGATA[A/G]CCCAGAATTTTCTGT	218038
rs29235057	snp	A/T	0.49827	0.0293608	intron-variant	Amph	Mm_Celera	13:19118073	CTGAAGAATGTTGTC[A/T]CTGGACAATGTGAGA	218038
rs29235173	snp	C/G/T	0.444444	0.157135	intron-variant	Amph	GRCm38.p3	13:19067656	TGATTGTTTTATGCC[C/G/T]CCCCTGTGAAGACTA	218038
rs29235361	snp	A/C	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19052979	AACTACTAACACGGG[A/C]TTGGCAACACAAATG	218038
rs29235365	snp	C/T	0.5	0	intron-variant	Amph	GRCm38.p3	13:19138875	TCAGTATGTGCCAGG[C/T]CACATGGGCGGTCAT	218038
rs29236439	snp	A/G	0.475309	0.108333	intron-variant	Amph	Mm_Celera	13:19084008	AATGACACTGTTAAC[A/G]TTTCCTGAGACCCAG	218038
rs29236649	snp	A/G	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19140203	AGGCAGGTCCTCACC[A/G]CGTGACCTTCTGCTT	218038
rs29237058	snp	A/G	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:19134580	GTACCAATTACTAAT[A/G]ATTTGTGCTGCTCAG	218038
rs29240458	snp	A/C	0.5	0	intron-variant	Amph	Mm_Celera	13:19135552	ATATGAATGACAGTT[A/C]ATCATGTATCCAACG	218038
rs29240701	snp	A/G	0.465374	0.126941	intron-variant	Amph	Mm_Celera	13:19085652	GACATTTGAACCCTC[A/G]GCTCCAGTTTCAAAC	218038
rs29241095	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19100050	TTACCAACTAGTTTG[C/T]TGATGTACATACATG	218038
rs29241106	snp	A/G	0.497041	0.0383476	intron-variant	Amph	Mm_Celera	13:19101277	GGGTCATTTTGCTTT[A/G]TTTTCCTTATTGAAG	218038
rs29242021	snp	C/T	0.290657	0.246672	intron-variant	Amph	Mm_Celera	13:19121255	TTTTTTTTAATGGCC[C/T]ATTTTCTTTCAATTT	218038
rs29243069	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19067699	CCCAGAAACACTATG[C/T]AAACTTCCAAAAGAA	218038
rs29243077	snp	A/C	0.444444	0.157135	intron-variant	Amph, Gm31887	Mm_Celera	13:19146794	CAGTATTTCTAGCTG[A/C]TTCCAAATATTTGGA	218038
rs29243519	snp	C/T	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19121447	TTTTTTTATGGCTTC[C/T]CCCTTTTCTCAGAAA	218038
rs29243820	snp	A/G	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19097508	AAAATGCGTGAAATC[A/G]GGGTCACAGGGTTAC	218038
rs29244042	snp	C/T	0.415225	0.187619	intron-variant	Amph	GRCm38.p3	13:19123218	ATTCTCATCACTGAG[C/T]GTTTTCAGAATATGT	218038
rs29244260	snp	A/G	0.387812	0.208586	intron-variant	Amph	Mm_Celera	13:19110681	GTTGAATATTTTACT[A/G]CACATAATAAATGAT	218038
rs29245326	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19134783	AGGTGTAGTTCTGTT[C/T]AAGACAGATGAAAAG	218038
rs29245821	snp	C/G	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:19097919	TGACTCCTGGTTCCA[C/G]TAACCCTCAAGTTTT	218038
rs29245958	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19100028	AAGCACAGGGCATTG[C/T]ATAGAATTACCAACT	218038
rs29247186	snp	A/G	0.495868	0.0452663	intron-variant	Amph	GRCm38.p3	13:19132939	ATTACAAAGTCTCCT[A/G]CAGCTTCCACCTTGG	218038
rs29248051	snp	G/T	0.5	0	intron-variant	Amph	Mm_Celera	13:19078722	CTCACCAAAGAATGG[G/T]GAAGATGACAATGAC	218038
rs29248423	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19079749	CTGTGTGCTGGACTC[C/T]GTGCTAAGCACTTTA	218038
rs29248685	snp	C/T	0.49827	0.0293608	downstream-variant-500B, intron-variant	Amph, Gm31887	GRCm38.p3	13:19154111	GCACATGGCGGAATC[C/T]TGGACCTGCTGAATT	218038
rs29249718	snp	A/C	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19069271	TTTTGCCAAAAGATA[A/C]AAAAAGTGTTTAATT	218038
rs29250399	snp	A/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19052822	AAGAGTAACAACAAG[A/T]AGACACAGATCACCA	218038
rs29250807	snp	C/T	0.5	0	intron-variant	Amph	Mm_Celera	13:19138778	TTATAGAAGCTTATC[C/T]CAGTTTTCAAGGAAA	218038
rs29251637	snp	A/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19079908	CAATTATATTAAAAT[A/G]TAAATCTCTCTCTCT	218038
rs29251812	snp	A/C	0.497778	0.0332592	intron-variant	Amph	Mm_Celera	13:19117233	TAGAAGCTACACATG[A/C]CTAAGACATGTTTAC	218038
rs29492531	snp	G/T	0.375	0.216506	intron-variant	Amph	GRCm38.p3	13:19097301	TGCCTCTGACAAGAA[G/T]CCCGAGGACCAGAGA	218038
rs29493212	snp	A/C	0.429688	0.173817	intron-variant	Amph	GRCm38.p3	13:19117350	CTAACCTCAACTTTG[A/C]ATTCCTTTTATTATT	218038
rs29493258	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19053064	CCCCATGTTGTTCTG[C/T]TGAAGAGTCAAGACA	218038
rs29493726	snp	G/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19108836	ATAGAGGCTCAGGTG[G/T]GGGGGGGTGGTGTAA	218038
rs29494576	snp	C/T	0.5	0	intron-variant	Amph	GRCm38.p3	13:19136393	TGATCCCCTCTGATC[C/T]CCTCATCCCCTAGTG	218038
rs29495440	snp	A/G	0.432133	0.171253	intron-variant	Amph	Mm_Celera	13:19120639	CCCAGGTAAGGAGAC[A/G]GTTTTTCTTATGAGA	218038
rs29496962	snp	A/G	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19095981	TGTGCTCCGCTGTGT[A/G]TAAATGTGTTGTGTG	218038
rs29509132	snp	A/G	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19108607	TCTTTGCCCCATAGG[A/G]CCCATGAACTATTGA	218038
rs29511162	snp	C/T	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19120403	CATCTTCCCCCCCCC[C/T]TTTTTTTTTGTCAGC	218038
rs29511691	snp	C/G	0.456747	0.140554	intron-variant	Amph	Mm_Celera	13:19097649	TTTCAGAGTTCTTAC[C/G]TTTGGCTCCCAGTTT	218038
rs29513181	snp	C/T	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19085689	CTTTGGACAATAAAG[C/T]GATCATTATATGTTC	218038
rs29513753	snp	A/G	0.32	0.24	intron-variant	Amph	GRCm38.p3	13:19100075	TACATGGATACTGTA[A/G]TACTGTGTATTACTC	218038
rs29514085	snp	C/T	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19071107	CTTGAAACACAGGCC[C/T]TTTTCTAGATATGAG	218038
rs29515066	snp	C/T	0.444444	0.157135	intron-variant	Amph	GRCm38.p3	13:19134128	AGGAGAGCTACGATG[C/T]ATAGTATATCTTGTG	218038
rs29515169	snp	A/G	0.5	0	intron-variant	Amph	Mm_Celera	13:19103226	CCTTTGGCTTTTCTA[A/G]CCCCATCCCCACCTT	218038
rs29528489	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19079926	AATCTCTCTCTCTCT[C/T]TCTCTCTCTCTCTCT	218038
rs29528501	snp	A/G	0.49827	0.0293608	intron-variant	Amph	GRCm38.p3	13:19112253	CTTTCATTCTGTGTC[A/G]CAGCTACTTACCTGC	218038
rs29528837	snp	C/T	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19073551	TAACATTGGAGAAAG[C/T]GGAGAAATCATTAGA	218038
rs29529353	snp	A/G	0.375	0.216506	intron-variant	Amph	GRCm38.p3	13:19128858	TGACCACAGTGACCT[A/G]AGGAAGAAAAGGATT	218038
rs29533260	snp	C/G	0.359862	0.224567	intron-variant	Amph	Mm_Celera	13:19123329	CATAGCATGTTACTG[C/G]CCCATTAACATCTGT	218038
rs29535216	snp	A/G	0.5	0	intron-variant	Amph	GRCm38.p3	13:19138896	GGGCGGTCATGAACA[A/G]CCATGGCAAACCCTC	218038
rs29546050	snp	C/T	0.484429	0.0868505	intron-variant	Amph	Mm_Celera	13:19078860	TTTGACACAGCACTT[C/T]ACTCCTAAGATGATA	218038
rs29547259	snp	A/T	0.32	0.24	intron-variant	Amph	GRCm38.p3	13:19117797	GCATGGAGGCATTTC[A/T]TGTCCTCTATGCTTG	218038
rs29548671	snp	C/T	0.375	0.216506	intron-variant	Amph	GRCm38.p3	13:19139876	TGGGAAGAAAGATTT[C/T]CTGGCCAGGGACTAA	218038
rs29550226	snp	C/G	0.444444	0.157135	intron-variant	Amph	GRCm38.p3	13:19138212	TTTAGCCTACTCAAG[C/G]CTGGGGGAAGGGCAC	218038
rs29551283	snp	C/T	0.497778	0.0332592	downstream-variant-500B, intron-variant	Amph, Gm31887	GRCm38.p3	13:19154170	AGGAACACACACCCA[C/T]TGTTGTCTCTTCCCT	218038

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