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
rs27353568	snp	C/T	0.444444	0.157135	intron-variant	Nsfl1c	Mm_Celera	2:151509479	CCTTGTTTCTTTCTA[C/T]ACTGCCCTGATGTTC	386649
rs27353569	snp	A/G	0.32	0.24	intron-variant	Nsfl1c	Mm_Celera	2:151509461	CTTGTACCTCTGTGA[A/G]GACCTTGTTTCTTTC	386649
rs27353570	snp	C/T	0.444444	0.157135	intron-variant	Nsfl1c	Mm_Celera	2:151509294	GCCATGTCAGTGAAG[C/T]TGAGCCATCCTGATC	386649
rs27353571	snp	A/G	0.124444	0.216185	intron-variant	Nsfl1c	Mm_Celera	2:151509207	GGGTGCCTGCCTGAA[A/G]AACATAACACAGCCA	386649
rs27353572	snp	A/C/G	0.336735	0.234472	intron-variant	Nsfl1c	GRCm38.p3	2:151508929	ATAAAATAAATGCCC[A/C/G]TGTGAGTTCATTAGT	386649
rs27353573	snp	C/T	0.124444	0.216185	intron-variant	Nsfl1c	Mm_Celera	2:151508809	TGTGAGCACAAATAA[C/T]TGGCAGAAGCTCCAT	386649
rs27353574	snp	C/T	0.124444	0.216185	intron-variant	Nsfl1c	Mm_Celera	2:151508547	GGCTCCACTTTTAAT[C/T]CTCTCAGCCCCTATC	386649
rs27353575	snp	A/G	0.32	0.24	intron-variant	Nsfl1c	Mm_Celera	2:151508509	AAAGCAGCTTCTCAC[A/G]GGTGTATGGTTGGTA	386649
rs27353576	snp	C/T	0.124444	0.216185	intron-variant	Nsfl1c	Mm_Celera	2:151508465	CCACTGTCCCAGGCT[C/T]GGGTCTTACAGGCCA	386649
rs27353577	snp	A/G	0.32	0.24	intron-variant	Nsfl1c	Mm_Celera	2:151506796	TTCCTGTCCAGCACC[A/G]TCTCCCAGGAGTGCT	386649
rs27353578	snp	C/T	0.260355	0.249785	intron-variant	Nsfl1c	Mm_Celera	2:151506209	TAATCAGGTTTCCAT[C/T]CATCTCAAAATAAAC	386649
rs27353579	snp	A/T	0.142012	0.225474	intron-variant	Nsfl1c	Mm_Celera	2:151505611	TTTTAGCTGTTTTCC[A/T]TGAGGCATAGCTAAG	386649
rs27353580	snp	C/T	0.32	0.24	intron-variant	Nsfl1c	Mm_Celera	2:151505575	TAAAGATTCACAGAT[C/T]ACTCCAAAAACCTTG	386649
rs27353581	snp	A/G	0.244898	0.249948	intron-variant	Nsfl1c	Mm_Celera	2:151505516	TGAGCTGTCAGGTGG[A/G]AAAGGAAGAAAAGTT	386649
rs27353582	snp	A/G	0.142012	0.225474	intron-variant	Nsfl1c	Mm_Celera	2:151505161	CTTCTCCTAACCTGC[A/G]TCATAGCATGTCCCT	386649
rs27353583	snp	G/T	0.244898	0.249948	intron-variant	Nsfl1c	Mm_Celera	2:151504588	CACACCCTCCAGGCA[G/T]TGATACTATATAATT	386649
rs27353584	snp	C/G	0.493827	0.0552116	intron-variant	Nsfl1c	Mm_Celera	2:151504496	AGAACCTTGAAAATG[C/G]CAAAGAAGGCCTGAA	386649
rs27353585	snp	C/G	0.277778	0.248452	intron-variant	Nsfl1c	Mm_Celera	2:151504476	GGTATTTTGGGGATA[C/G]TTGAAGAACCTTGAA	386649
rs27353586	snp	A/T	0.345679	0.230967	intron-variant	Nsfl1c	Mm_Celera	2:151504357	GTTTTCACTTGGTGG[A/T]TAGAGGGCCAGGGCA	386649
rs27353587	snp	A/T	0.32	0.24	intron-variant	Nsfl1c	Mm_Celera	2:151503899	TGAGTTTATACTGAG[A/T]ATAGTAGCTATTCCC	386649
rs27353588	snp	C/T	0.21875	0.248039	intron-variant	Nsfl1c	Mm_Celera	2:151503261	TCTAGCAGAGATTGG[C/T]TCCTTTGTTTCTTCA	386649
rs27353589	snp	A/G	0.124444	0.216185	synonymous-codon	Nsfl1c	Mm_Celera	2:151503176	AGAGACCAGTAAACC[A/G]AGAGTGAGCATAAGG	386649
rs27353590	snp	C/T	0.297521	0.245442	intron-variant	Nsfl1c	Mm_Celera	2:151502897	CTGCTTGCACCCTTA[C/T]GTGTTTTTCTAGCTA	386649
rs27353591	snp	C/T	0.48	0.0979796	intron-variant	Nsfl1c	Mm_Celera	2:151502886	TTGCATCATATCTGC[C/T]TGCACCCTTATGTGT	386649
rs27353592	snp	C/T	0.152778	0.230321	intron-variant	Nsfl1c	Mm_Celera	2:151502317	CATCTCTTGAGGCTC[C/T]CAATGTACATCATAA	386649
rs27353593	snp	C/G	0.5	0	intron-variant	Nsfl1c	Mm_Celera	2:151502310	TCTAGTGCATCTCTT[C/G]AGGCTCCCAATGTAC	386649
rs27353594	snp	C/T	0.444444	0.157135	intron-variant	Nsfl1c	Mm_Celera	2:151502308	CTTCTAGTGCATCTC[C/T]TGAGGCTCCCAATGT	386649
rs27353595	snp	A/G	0.197531	0.244432	intron-variant	Nsfl1c	Mm_Celera	2:151501023	TTTCTCTCTCTAATT[A/G]TTACAGGGAGGTATT	386649
rs27353596	snp	G/T	0.18	0.24	intron-variant	Nsfl1c	Mm_Celera	2:151500934	GAGCAGTTTGCTCTC[G/T]GTAGGTTAGCAGTAA	386649
rs27353597	snp	G/T	0.244898	0.249948	intron-variant	Nsfl1c	Mm_Celera	2:151500913	CATAGGGGTATAATA[G/T]CCTAAGAGCAGTTTG	386649
rs27353598	snp	A/G	0.260355	0.249785	intron-variant	Nsfl1c	Mm_Celera	2:151500541	TATTCTCAGTCCTGT[A/G]TGACCTTAACAGACA	386649
rs27353599	snp	C/T	0.345679	0.230967	intron-variant	Nsfl1c	Mm_Celera	2:151500096	TATAGTAGATAGTTG[C/T]TTATCTGTGCCACTA	386649
rs27353600	snp	A/T	0.297521	0.245442	intron-variant	Nsfl1c	Mm_Celera	2:151499985	TTGGTAATGGTCCAA[A/T]TGTGCCTTTTTGTAG	386649
rs27353601	snp	A/G	0.277778	0.248452	intron-variant	Nsfl1c	Mm_Celera	2:151499964	AGTCTCCTGTTCACC[A/G]GTTCCTTGGTAATGG	386649
rs27353602	snp	A/C	0.444444	0.157135	intron-variant	Nsfl1c	Mm_Celera	2:151499597	CTGCTGAAGCCAGAG[A/C]TAACCCCTCAAACTT	386649
rs27353603	snp	A/G	0.42	0.183303	intron-variant	Nsfl1c	Mm_Celera	2:151499573	AGAGTTTTTGCACTA[A/G]CCATCTGTCTGCTGA	386649
rs27353604	snp	A/G	0.132653	0.220748	intron-variant	Nsfl1c	Mm_Celera	2:151499506	CTCTCATGTTGTCTT[A/G]AACCCTTTTCCTGAT	386649
rs27353605	snp	A/G	0.336735	0.234472	intron-variant	Nsfl1c	Mm_Celera	2:151498884	TATACTTTGGCAGGT[A/G]TCTTCTGGCAAGAGA	386649
rs27353606	snp	C/T	0.277778	0.248452	intron-variant	Nsfl1c	Mm_Celera	2:151498682	AGCTGTTACAGGACA[C/T]TTAGCCTGCTGCTGA	386649
rs27353607	snp	G/T	0.444444	0.157135	intron-variant	Nsfl1c	Mm_Celera	2:151498505	CTTTGACTGTGGGCT[G/T]CTGTGAAGGACAAAA	386649
rs27353608	snp	C/T	0.336735	0.234472	intron-variant	Nsfl1c	Mm_Celera	2:151498408	GCTACAGCTTAACAT[C/T]AGCATTAAACGTGAA	386649
rs27353609	snp	C/T	0.5	0	intron-variant	Nsfl1c	Mm_Celera	2:151498268	CTATGACTGACACTG[C/T]ACCCTGCCTCATTCC	386649
rs27353610	snp	C/T	0.297521	0.245442	intron-variant	Nsfl1c	Mm_Celera	2:151497806	TCCTCTCTTCTTCCA[C/T]AGTCCAGAATAACCC	386649
rs27353611	snp	A/G	0.345679	0.230967	intron-variant	Nsfl1c	Mm_Celera	2:151497753	AGTACCAAGGAGGAG[A/G]AATTGAAATGTAGCC	386649
rs27353612	snp	A/G	0.375	0.216506	intron-variant	Nsfl1c	Mm_Celera	2:151497333	TCTCTCTACAGAAGC[A/G]TCTGAGCTCCCACAC	386649
rs27353613	snp	C/G	0.152778	0.230321	intron-variant	Nsfl1c	Mm_Celera	2:151497214	TTCTGAAGTTGACAC[C/G]GGGAGTTAACTAACA	386649
rs27353614	snp	A/G	0.152778	0.230321	intron-variant	Nsfl1c	Mm_Celera	2:151497209	ACCTCTTCTGAAGTT[A/G]ACACGGGGAGTTAAC	386649
rs27353615	snp	A/G	0.297521	0.245442	intron-variant	Nsfl1c	Mm_Celera	2:151497162	TGAGGTTAATGGCCT[A/G]TCACACTAGTAAGAT	386649
rs27353616	snp	A/G	0.142012	0.225474	intron-variant	Nsfl1c	Mm_Celera	2:151497150	CCATAGTAGAGATGA[A/G]GTTAATGGCCTGTCA	386649
rs27353619	snp	A/G	0.277778	0.248452	intron-variant	Nsfl1c	Mm_Celera	2:151495965	GGACTCATATGAAGG[A/G]CTTTCACATGTGTAA	386649
rs27353620	snp	A/G	0.197531	0.244432	intron-variant	Nsfl1c	Mm_Celera	2:151495919	AATCAATGCCTTCTC[A/G]TTGAGTTGGCGACAG	386649
rs27353621	snp	C/T	0.375	0.216506	intron-variant	Nsfl1c	Mm_Celera	2:151495846	CAGGAGGTGCCTCCT[C/T]CATCTCCGTGGGACT	386649
rs27353622	snp	C/T	0.165289	0.235211	intron-variant	Nsfl1c	Mm_Celera	2:151495672	TAACTTGACTAGCAG[C/T]GCCAGGACTTGAATG	386649
rs27353623	snp	A/G	0.408163	0.193609	intron-variant	Nsfl1c	Mm_Celera	2:151495668	GTGGTAACTTGACTA[A/G]CAGTGCCAGGACTTG	386649
rs27353624	snp	C/T	0.132653	0.220748	intron-variant	Nsfl1c	Mm_Celera	2:151495319	AAAGACTAACCCTAT[C/T]TTATGGATAAGGAAT	386649
rs27353625	snp	A/G	0.336735	0.234472	synonymous-codon	Nsfl1c	Mm_Celera	2:151494364	GGTGACTGGCACTGA[A/G]GAGGACAGGGCCCGT	386649
rs27353626	snp	C/T	0.124444	0.216185	utr-variant-5-prime	Nsfl1c	Mm_Celera	2:151494273	GGGCTGTTGCAGTGT[C/T]CGCCGGAGCGGTTTG	386649
rs27353627	snp	A/G	0.375	0.216506	utr-variant-5-prime	Nsfl1c	Mm_Celera	2:151494199	TGGGCGGAGCCTACG[A/G]GCAGGCGCCCAGCGG	386649
rs27353628	snp	A/G	0.244898	0.249948	upstream-variant-2KB	Nsfl1c	Mm_Celera	2:151494136	GCCACCAGAGGGCGC[A/G]AGGCGGCTAGGTTTC	386649
rs27353629	snp	A/G	0.124444	0.216185	upstream-variant-2KB	Nsfl1c	Mm_Celera	2:151494032	AGGATCTGATTTCGG[A/G]ACTACTTCATCCTGT	386649
rs27353630	snp	C/G	0.124444	0.216185	upstream-variant-2KB	Nsfl1c	Mm_Celera	2:151493941	CAAGCCATAGACAGC[C/G]TAATGCTTCAAGAAG	386649
rs27353631	snp	A/G	0.132653	0.220748	upstream-variant-2KB	Nsfl1c	Mm_Celera	2:151493745	AGCCTGCCAGTGGCA[A/G]TGCAATGGTGATTTG	386649
rs27353632	snp	A/G	0.4032	0.19756	upstream-variant-2KB	Nsfl1c	Mm_Celera	2:151493516	TCAATAAGTTCTGGT[A/G]GAATAATTGCTGGTC	386649
rs27353633	snp	A/G	0.497041	0.0383476	upstream-variant-2KB	Nsfl1c	Mm_Celera	2:151493470	AGAAAAACAAAGCAT[A/G]TAATCAGCTGACAGG	386649
rs27353634	snp	C/T	0.152778	0.230321	upstream-variant-2KB	Nsfl1c	Mm_Celera	2:151493407	ATTCATTAGTAGTGG[C/T]TTCATGCACAGTGAA	386649
rs27353635	snp	A/G	0.132653	0.220748	upstream-variant-2KB	Nsfl1c	Mm_Celera	2:151493273	GCTCTTCATTCTCAT[A/G]GTATGACTCTGTGGA	386649
rs27353636	snp	A/G	0.426035	0.177515	upstream-variant-2KB	Nsfl1c	GRCm38.p3	2:151492761	TAAATATGCTCTGCA[A/G]GGTCACTCTTTCAGT	386649
rs27353637	snp	G/T	0.124444	0.216185	upstream-variant-2KB	Nsfl1c	GRCm38.p3	2:151492694	GCATCCTCTGCCTTT[G/T]AGCATGGATTCACTT	386649
rs27353638	snp	A/G	0.142012	0.225474	upstream-variant-2KB	Nsfl1c	GRCm38.p3	2:151492574	GACAGCGAAGATAGA[A/G]GCTTGGTCAGTCTTT	386649
rs27353639	snp	A/C	0.132653	0.220748	upstream-variant-2KB	Nsfl1c	GRCm38.p3	2:151492507	AGCTTTAAATTGAAA[A/C]CAGAACTTGACCACA	386649
rs27353640	snp	A/G	0.132653	0.220748	upstream-variant-2KB	Nsfl1c	GRCm38.p3	2:151492392	CTGGAAGCCATGAGT[A/G]TTGTGTGGAGTGCCC	386649
rs27402538	snp	C/G	0.32	0.24	downstream-variant-500B	Nsfl1c	Mm_Celera	2:151511701	GGTATGTATAGTTAA[C/G]GTGTAGCTTTGGGAC	386649
rs27402539	snp	C/G	0.124444	0.216185	downstream-variant-500B	Nsfl1c	Mm_Celera	2:151511685	GAAGCAATTTTATTT[C/G]GGTATGTATAGTTAA	386649
rs27402540	snp	A/T	0.124444	0.216185	downstream-variant-500B	Nsfl1c	Mm_Celera	2:151511603	GCAGCAGATACACAT[A/T]TGGGAATGAATGTCT	386649
rs27402541	snp	A/G	0.152778	0.230321	downstream-variant-500B	Nsfl1c	Mm_Celera	2:151511545	AGTGGGTTCAGGTAG[A/G]TGTCTTTTTCTAGGA	386649
rs27402542	snp	C/T	0.197531	0.244432	downstream-variant-500B	Nsfl1c	Mm_Celera	2:151511542	CTTAGTGGGTTCAGG[C/T]AGGTGTCTTTTTCTA	386649
rs27402543	snp	A/T	0.444444	0.157135	downstream-variant-500B	Nsfl1c	Mm_Celera	2:151511505	ATAGAGGGGTTTTCT[A/T]TTGGATGTGGCACAT	386649
rs27402544	snp	A/C	0.32	0.24	downstream-variant-500B	Nsfl1c	Mm_Celera	2:151511428	AAGTCACTGTGTACA[A/C]ATAATCATCTCCTGC	386649
rs27402545	snp	A/G	0.32	0.24	utr-variant-3-prime	Nsfl1c	Mm_Celera	2:151511173	CCCTTCCAGTGCCAC[A/G]TCTCGTCCGTAGCTC	386649
rs27402546	snp	C/T	0.124444	0.216185	utr-variant-3-prime	Nsfl1c	Mm_Celera	2:151511114	TGTCTCCCATGACTG[C/T]GGCCATGCCCGTGGG	386649
rs27402547	snp	A/T	0.32	0.24	intron-variant	Nsfl1c	Mm_Celera	2:151510380	TCCCAGGTGCAAGAA[A/T]GTGCCTGGAGGAGGG	386649
rs27402548	snp	C/T	0.124444	0.216185	intron-variant	Nsfl1c	Mm_Celera	2:151510336	GGTATAAGGAAGAAT[C/T]CTGTTGCCAGTGGCT	386649
rs27402549	snp	C/T	0.444444	0.157135	intron-variant	Nsfl1c	Mm_Celera	2:151510127	ACCAAATGTTCCTAA[C/T]GTTGGTGCTTCCCTC	386649
rs27402550	snp	A/G	0.124444	0.216185	intron-variant	Nsfl1c	Mm_Celera	2:151510104	AGGTAGGCAATCTTT[A/G]AGTGCTGACCAAATG	386649
rs27402551	snp	G/T	0.408163	0.193609	intron-variant	Nsfl1c	Mm_Celera	2:151510051	GTTTCATCCATAGTG[G/T]GCTAGCTAAGCCAGG	386649
rs27402552	snp	A/G	0.32	0.24	intron-variant	Nsfl1c	Mm_Celera	2:151510008	TAAAGATACTTGGCA[A/G]CTCCTTTCTCTCAAA	386649
rs27402553	snp	A/G	0.408163	0.193609	intron-variant	Nsfl1c	Mm_Celera	2:151509967	TGAAGAGACTAGCAG[A/G]AGAGGTGCTAGGGGC	386649
rs27402554	snp	A/C	0.391111	0.206368	intron-variant	Nsfl1c	Mm_Celera	2:151509869	TAGGTCTCATTCCTC[A/C]TCATTAGGATTAAGC	386649
rs27402555	snp	C/T	0.32	0.24	intron-variant	Nsfl1c	Mm_Celera	2:151509683	CCACAGGTACCTTCT[C/T]TATCTGGACTACCTT	386649
rs27402556	snp	C/T	0.142012	0.225474	synonymous-codon	Nsfl1c	Mm_Celera	2:151509536	GGTATTAAACACCAG[C/T]TCTCCAGCCCAACAA	386649
rs45947017	snp	A/G			intron-variant	Nsfl1c	Mm_Celera	2:151496383	TCTTTGTTTCCCTTG[A/G]TGGGTGGATTTCCCC	386649
rs46427525	snp	A/G			intron-variant	Nsfl1c	Mm_Celera	2:151496327	GATAAATAATAGTTG[A/G]TGGTCTTCCTTTATG	386649
rs47166990	snp	A/G			intron-variant	Nsfl1c	Mm_Celera	2:151496349	TCCTTTATGTTTTTC[A/G]TATTAATTTTATTTA	386649
rs48897904	snp	A/G			intron-variant	Nsfl1c	Mm_Celera	2:151496365	TATTAATTTTATTTA[A/G]TATCTTTGTTTCCCT	386649
rs50446547	snp	C/G			intron-variant	Nsfl1c	Mm_Celera	2:151496326	GGATAAATAATAGTT[C/G]GTGGTCTTCCTTTAT	386649
rs50850311	snp	C/T			intron-variant	Nsfl1c	Mm_Celera	2:151496376	TTTAGTATCTTTGTT[C/T]CCCTTGGTGGGTGGA	386649
rs107677296	snp	G/T			intron-variant	Nsfl1c	Mm_Celera	2:151496975	AGTTAATACATGATT[G/T]TGGGCCACCATGTGG	386649
rs107954411	snp	C/T			intron-variant	Nsfl1c	Mm_Celera	2:151496949	GAAGGCATTGGATTT[C/T]CTGAAACTGGAGTTA	386649
rs108547543	snp	A/G			intron-variant	Nsfl1c	Mm_Celera	2:151496887	TTGTTTTGAATGTGA[A/G]TGGGTGTTCTGCCTG	386649
rs211718042	snp	C/G			intron-variant	Nsfl1c	Mm_Celera	2:151505485	GAAAAGCCCATGTTA[C/G]TCTCACTTTCGTGAA	386649

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