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
rs3724626	snp	A/T	0.32	0.24	intron-variant, upstream-variant-2KB	Six4, Mnat1	Mm_Celera	12:73110255	GTGGCCTTGTCACTA[A/T]CAGACTCCTGCCCTG	17420
rs3725726	snp	C/T	0.32	0.24	intron-variant, upstream-variant-2KB	Six4, Mnat1	Mm_Celera	12:73110400	AAGCAGTTTGGAAGC[C/T]TGGTGAGACTTGGTC	17420
rs6210064	snp	A/G	0.5	0	intron-variant	Mnat1	Mm_Celera	12:73149393	tttcaatgctatctg[A/G]gcagcttggttaaat	17420
rs6210156	snp	A/C	0.48	0.0979796	intron-variant	Mnat1	Mm_Celera	12:73149441	AGTAAAAGCTGAGGG[A/C]TGGTGGGATTGCTCA	17420
rs6210653	snp	C/T	0.5	0	intron-variant	Mnat1	Mm_Celera	12:73149513	tgatctcagaagcct[C/T]atggtggaagcagag	17420
rs6224615	snp	A/G	0.5	0	intron-variant	Mnat1	Mm_Celera	12:73149781	acacacacatacatg[A/G]atatgcacacataca	17420
rs6225653	snp	A/C	0.231111	0.249285	intron-variant	Mnat1	Mm_Celera	12:73149956	AAAAGGGCTCTATAT[A/C]TTATGGTATGTTTTT	17420
rs6260915	snp	A/G	0.5	0	intron-variant	Mnat1	Mm_Celera	12:73185223	TCTAGAGACATGCTT[A/G]TCACCACAACCCATG	17420
rs6278611	snp	C/T	0.5	0	intron-variant	Mnat1	GRCm38.p3	12:73186186	tcaaactcaggtacc[C/T]gggcctttgggcaag	17420
rs6279595	snp	A/G	0.497041	0.0383476	intron-variant	Mnat1	Mm_Celera	12:73186393	ACTTGTTGCAGACAC[A/G]CACAGCAATGCAGTG	17420
rs6308785	snp	A/G	0.5	0	intron-variant	Mnat1	Mm_Celera	12:73193731	AGTAGAGCATTATGG[A/G]AATGCAAGCACAAAT	17420
rs6309780	snp	A/G	0.475309	0.108333	intron-variant	Mnat1	Mm_Celera	12:73193877	AATTATGTGTCTGTT[A/G]CTACTATTTCCAGTT	17420
rs6309869	snp	C/G	0.304688	0.243945	intron-variant	Mnat1	Mm_Celera	12:73193940	GACAGTCTAAGTAGA[C/G]GACACAGAGCTCATC	17420
rs6310323	snp	A/G	0.231111	0.249285	intron-variant	Mnat1	Mm_Celera	12:73193996	TCCCACCTGCTACCT[A/G]TAGCAACCTGAGTAT	17420
rs6311516	snp	G/T	0.5	0	intron-variant	Mnat1	Mm_Celera	12:73194261	cagaagagggagtca[G/T]atctcattacngatg	17420
rs6311535	snp	A/G	0.5	0	intron-variant	Mnat1	Mm_Celera	12:73194272	gtcanatctcattac[A/G]gatggttgtgaccca	17420
rs6312539	snp	C/T	0.489796	0.070696	intron-variant	Mnat1	Mm_Celera	12:73194427	AAGGATGATGACAAA[C/T]AAGCAACATTGAAAA	17420
rs6344555	snp	A/T	0.444444	0.157135	downstream-variant-500B, intron-variant	Mnat1, Trmt5	Mm_Celera	12:73274272	CGTCTCCCGTGTTCT[A/T]GCAGATAGAGGTGTC	17420
rs6345120	snp	C/T	0.5	0	downstream-variant-500B, intron-variant	Mnat1, Trmt5	Mm_Celera	12:73274365	GCCAGGAGTTAAACT[C/T]CAGTGCCAAGGCTCC	17420
rs6356996	snp	G/T	0.5	0	intron-variant	Mnat1	Mm_Celera	12:73208948	TATGTTTGTTTGTTT[G/T]TTGTTTTTTGTTTTG	17420
rs6357488	snp	C/T	0.5	0	intron-variant	Mnat1	Mm_Celera	12:73209053	CTGTACAAGTTGTCA[C/T]CATCACTGGCCAACT	17420
rs6357519	snp	A/G	0.304688	0.243945	intron-variant	Mnat1	Mm_Celera	12:73209069	CATCACTGGCCAACT[A/G]TGAGTTCANTTCTGG	17420
rs6357912	snp	C/G	0.207612	0.24638	intron-variant	Mnat1	Mm_Celera	12:73209078	CCAACTNTGAGTTCA[C/G]TTCTGGTGTCACAAT	17420
rs6394401	snp	C/T	0.5	0	intron-variant	Mnat1	Mm_Celera	12:73139151	AACTCAAGTTGtctc[C/T]ccttcccctctcttt	17420
rs6394962	snp	C/T	0.5	0	intron-variant	Mnat1	Mm_Celera	12:73139256	ccaccccTGCTGGGT[C/T]AGGATGGGATCCATT	17420
rs6395389	snp	A/G/T	0.5	0	intron-variant	Mnat1	Mm_Celera	12:73139288	CCACATGCATATTAG[A/G/T]CTAGCACTGTNTTAC	17420
rs6395411	snp	A/G	0.5	0	intron-variant	Mnat1	Mm_Celera	12:73139299	TTAGNCTAGCACTGT[A/G]TTACTGACTTAATGT	17420
rs29122859	snp	A/C	0.5	0	intron-variant	Mnat1	Mm_Celera	12:73118447	GTACTTGCTGAAGTA[A/C]TTATGTTTCTGGGTT	17420
rs29124329	snp	C/T	0.5	0	intron-variant	Mnat1	Mm_Celera	12:73257120	TTAGCAGTGGCAGCT[C/T]GATCCACTCACAAAA	17420
rs29124673	snp	G/T	0.5	0	intron-variant	Mnat1	Mm_Celera	12:73224985	CGACTGAAGATAGTA[G/T]GCGACTGTCTTAGCC	17420
rs29125002	snp	A/G	0.5	0	intron-variant	Mnat1	Mm_Celera	12:73161127	TGTATTTATTTATTT[A/G]TTTATTGTTTTGTTT	17420
rs29125443	snp	A/G	0.444444	0.157135	intron-variant	Mnat1	Mm_Celera	12:73191541	GTTGCCTGGAAGTCC[A/G]TCTTCCACTAGCAGC	17420
rs29125984	snp	A/G	0.375	0.216506	intron-variant	Mnat1	Mm_Celera	12:73205030	GTGAATATTTCAGGT[A/G]AATAATAATTTTCTT	17420
rs29126515	snp	A/T	0.5	0	intron-variant	Mnat1	Mm_Celera	12:73161135	TTATTTGTTTATTGT[A/T]TTGTTTTGTTTTTGT	17420
rs29126694	snp	C/T	0.444444	0.157135	intron-variant	Mnat1	Mm_Celera	12:73224929	AGGGCATACAGGGAG[C/T]CCCATCCTGTATCTC	17420
rs29127160	snp	A/T	0.444444	0.157135	intron-variant	Mnat1	Mm_Celera	12:73125020	GACAGCGTAACTGTG[A/T]CTGGATGGTTTAAGA	17420
rs29127163	snp	C/T	0.345679	0.230967	intron-variant	Mnat1	Mm_Celera	12:73195387	TTCACTGGGAAGATG[C/T]GCCATTTTATTTTAA	17420
rs29127193	snp	C/T	0.375	0.216506	intron-variant	Mnat1	Mm_Celera	12:73124960	TCTTTTTTTTTTTTT[C/T]CCACGACAGGGTCTC	17420
rs29127491	snp	A/G	0.5	0	intron-variant	Mnat1	Mm_Celera	12:73219247	CCTAAGTTAAGTTTT[A/G]GTCAGTGTATCGACT	17420
rs29128187	snp	G/T	0.444444	0.157135	intron-variant	Mnat1	Mm_Celera	12:73205568	CAAAATAATTTAATA[G/T]TAAATTATTTAAAAA	17420
rs29128309	snp	C/T	0.5	0	intron-variant	Mnat1	Mm_Celera	12:73138090	AGGTGCTCTTACCCA[C/T]TGAGCCATCTCACCA	17420
rs29129575	snp	A/G	0.32	0.24	intron-variant	Mnat1	Mm_Celera	12:73153512	GACAATTTAATTAAT[A/G]TAATAGGAGTTCATT	17420
rs29129832	snp	C/T	0.5	0	intron-variant	Mnat1	Mm_Celera	12:73230663	CTAATATTTTTTCTG[C/T]TCCAGGTTCTTTTCG	17420
rs29130119	snp	A/G	0.444444	0.157135	intron-variant	Mnat1	Mm_Celera	12:73144980	TCCTACAACATTCAT[A/G]CCCCACTCTTTCATA	17420
rs29130443	snp	A/G	0.444444	0.157135	intron-variant	Mnat1	Mm_Celera	12:73173521	CATATAACAATAAAT[A/G]AATCTTAAAAAATAA	17420
rs29130541	snp	A/G	0.444444	0.157135	intron-variant	Mnat1	Mm_Celera	12:73218956	GCGGAGCCATCTCTC[A/G]AAAATTACTACAAAT	17420
rs29130576	snp	C/T	0.48	0.0979796	intron-variant	Mnat1	Mm_Celera	12:73177129	TGGCCGAGTTATAGG[C/T]CAGCCTGGATTGCAA	17420
rs29130607	snp	C/T	0.375	0.216506	intron-variant	Mnat1	Mm_Celera	12:73260337	CCTCTACTCTCCTAA[C/T]CCTTCCATATCCACC	17420
rs29131232	snp	A/G	0.5	0	intron-variant	Mnat1	Mm_Celera	12:73132706	GGTGAGTACTTAGGA[A/G]ACTGACTAGGTTATG	17420
rs29131425	snp	A/C/T	0.375	0.216506	intron-variant	Mnat1	GRCm38.p3	12:73166367	TGCATGGGAAATGAA[A/C/T]AAAGCAGATTTTTAA	17420
rs29132000	snp	C/T	0.465374	0.126941	intron-variant	Mnat1	Mm_Celera	12:73226524	CACTTTCCACTGTCA[C/T]TGGACTGTAACTGAC	17420
rs29132084	snp	G/T	0.444444	0.157135	intron-variant	Mnat1	GRCm38.p3	12:73154731	TGTGTGAGAGAGAGT[G/T]TGTGTGAGTGTGTGA	17420
rs29132984	snp	G/T	0.465374	0.126941	intron-variant	Mnat1	Mm_Celera	12:73205837	TTTTGCTAGATCAAT[G/T]ATCAAGTGTGGTAAT	17420
rs29133176	snp	A/G	0.49827	0.0293608	intron-variant	Mnat1	Mm_Celera	12:73198900	ATAACAGCACATGTT[A/G]ATGAGGTGTGTCTGT	17420
rs29133196	snp	C/T	0.48	0.0979796	intron-variant	Mnat1	Mm_Celera	12:73153995	AAATTTTAGGGCAAG[C/T]CTGGGCTACATAGTG	17420
rs29133522	snp	A/C	0.444444	0.157135	intron-variant	Mnat1	GRCm38.p3	12:73218515	TAAAACAAAACAAAA[A/C]ACCGATTACCAAATA	17420
rs29133562	snp	A/T	0.375	0.216506	intron-variant	Mnat1	Mm_Celera	12:73128854	GTTTTTTGTTTTTTT[A/T]AATTTAACTAAGTTG	17420
rs29133755	snp	A/C	0.46875	0.121031	intron-variant	Mnat1	Mm_Celera	12:73236171	TTTGTTATGTAAATA[A/C]ATTTTGTAAACTTAA	17420
rs29133844	snp	A/T	0.32	0.24	intron-variant	Mnat1	Mm_Celera	12:73233970	TCTCTGGGCTGGTAG[A/T]CTTGGGTTCTATAAG	17420
rs29134002	snp	C/T	0.444444	0.157135	intron-variant	Mnat1	Mm_Celera	12:73219890	ATGGATAATATTCTA[C/T]ATATGATTACTGAGG	17420
rs29134072	snp	A/T	0.444444	0.157135	intron-variant	Mnat1	Mm_Celera	12:73169511	CCTCTTAGTTCTTAT[A/T]TTTGGGGGTATACAT	17420
rs29134475	snp	C/T	0.444444	0.157135	intron-variant	Mnat1	Mm_Celera	12:73176446	TTGCCCTTTGTACTC[C/T]ACATCCATGCACACA	17420
rs29134794	snp	C/T	0.5	0	utr-variant-3-prime, intron-variant	Mnat1, Trmt5	Mm_Celera	12:73273675	CTTCCTTGCTAGAAG[C/T]CACACTTCTCATCTT	17420
rs29134892	snp	C/G	0.375	0.216506	intron-variant	Mnat1	Mm_Celera	12:73199117	TGTTGCTAGTGAGAA[C/G]AGGAAATGCTAGTGA	17420
rs29134910	snp	C/T	0.265928	0.249492	utr-variant-3-prime, intron-variant	Mnat1, Trmt5	Mm_Celera	12:73272624	GTTCCAGCCCCGCAG[C/T]TGCACAGCACACCAC	17420
rs29135350	snp	C/T	0.345679	0.230967	intron-variant	Mnat1	Mm_Celera	12:73224142	ATGCTCACGAGACTG[C/T]AGGTCACTGAGGAAA	17420
rs29135729	snp	C/T	0.444444	0.157135	intron-variant	Mnat1	Mm_Celera	12:73227152	CAATTAATTGTTCAC[C/T]TTATATGGTTTTCTT	17420
rs29136183	snp	A/G	0.375	0.216506	intron-variant	Mnat1	Mm_Celera	12:73256930	CCTCCCGAGTGCTGG[A/G]ATCAAAGGTGTGCAC	17420
rs29136912	snp	A/C	0.375	0.216506	intron-variant	Mnat1	Mm_Celera	12:73146362	TTGAAGGAAGTAAGC[A/C]TTCTAGTTAGATATG	17420
rs29136996	snp	C/T	0.304688	0.243945	intron-variant	Mnat1, Trmt5	Mm_Celera	12:73272312	TGAACATTTCAATCT[C/T]GGAATTCCTTTCCAA	17420
rs29137025	snp	C/T	0.5	0	intron-variant	Mnat1	Mm_Celera	12:73143231	AAATATCAACCCTTT[C/T]CCCCTTGAGTTGCAT	17420
rs29137321	snp	C/T	0.487535	0.077957	intron-variant	Mnat1	Mm_Celera	12:73203065	GGCTAGATAGCTTCT[C/T]CACAATGGCAGCTTT	17420
rs29137513	snp	C/T	0.375	0.216506	intron-variant	Mnat1	Mm_Celera	12:73179750	AGGCTCATAGACTCT[C/T]CCGGCTGCCTCTTCT	17420
rs29137606	snp	G/T	0.444444	0.157135	intron-variant	Mnat1	Mm_Celera	12:73125815	AATTAGTAAGTGGTG[G/T]TTATTTATTTTGAGT	17420
rs29137880	snp	A/G	0.444444	0.157135	intron-variant	Mnat1	Mm_Celera	12:73200152	TTCACTAAGTACAAG[A/G]TATAGGGGGAAGGCA	17420
rs29138837	snp	A/G	0.375	0.216506	intron-variant	Mnat1	Mm_Celera	12:73144108	CCTCCCCCCAGGGGG[A/G]AAAAATCTCATGAAA	17420
rs29139167	snp	G/T	0.444444	0.157135	intron-variant	Mnat1	GRCm38.p3	12:73139636	GTTTTTGTGACAGGG[G/T]TTGTCTGTGTAGCCC	17420
rs29139427	snp	A/G	0.444444	0.157135	intron-variant	Mnat1	Mm_Celera	12:73156699	GAGGTCCCATTTATC[A/G]ATTCTTGATTTTACA	17420
rs29139535	snp	C/T	0.277778	0.248452	intron-variant	Mnat1	Mm_Celera	12:73200788	CACAGTCACATTGTG[C/T]GGGTTCAGATTCTGG	17420
rs29139693	snp	C/T	0.5	0	intron-variant	Mnat1	Mm_Celera	12:73251233	GTATGAGTGGGTGTC[C/T]AACCCACACCTTGCT	17420
rs29140112	snp	A/G	0.32	0.24	intron-variant	Mnat1	Mm_Celera	12:73199274	ATAAAGCCGGTCGCC[A/G]CCAGGTGTAAGACTT	17420
rs29140324	snp	C/G	0.345679	0.230967	intron-variant	Mnat1	Mm_Celera	12:73230243	GGTTTTATAGTAAGT[C/G]TGAATATGACAGCAG	17420
rs29140442	snp	A/T	0.375	0.216506	intron-variant	Mnat1	Mm_Celera	12:73198061	CTTTTTTTCTAGATT[A/T]AAAAAAAAAGATTTA	17420
rs29140477	snp	A/C	0.444444	0.157135	intron-variant	Mnat1	Mm_Celera	12:73239736	AGACCTCAAAGCCCC[A/C]CCACCACAGTGATGC	17420
rs29140969	snp	C/T	0.5	0	intron-variant	Mnat1	Mm_Celera	12:73166155	ATCAGTATATAGCTC[C/T]CAGCTATTTCTCCAG	17420
rs29141284	snp	A/C/G	0.375	0.216506	intron-variant	Mnat1	GRCm38.p3	12:73208307	AGCACCTGCATGGTG[A/C/G]CTTGTTACAAACTCC	17420
rs29141355	snp	A/C	0.375	0.216506	intron-variant	Mnat1	Mm_Celera	12:73154884	TTTCTGACTCAACTA[A/C]TGCAGCTAGCTAGCT	17420
rs29141392	snp	C/T	0.375	0.216506	intron-variant	Mnat1	Mm_Celera	12:73257177	TTGGAATAGCAAACA[C/T]GAATCAGCAGCAGTG	17420
rs29141465	snp	G/T	0.265928	0.249492	intron-variant	Mnat1	Mm_Celera	12:73230513	GCAGCTTTGGAGTTT[G/T]AAAGTTAATATTGAG	17420
rs29141925	snp	A/G	0.304688	0.243945	intron-variant	Mnat1	Mm_Celera	12:73223602	TATACTTTGGTAAAG[A/G]GCTTTGCCTGTTGAA	17420
rs29142984	snp	C/T	0.5	0	intron-variant	Mnat1	Mm_Celera	12:73229503	GGTCCAGTGACCTCA[C/T]TCATTGGCACTTGTT	17420
rs29143209	snp	C/G	0.493827	0.0552116	intron-variant	Mnat1	Mm_Celera	12:73200221	TGTTTTATTTTAGCA[C/G]TGTGTCTCTTGTGTC	17420
rs29143446	snp	C/T	0.5	0	intron-variant	Mnat1	Mm_Celera	12:73209595	GCCACCCCTAACCTT[C/T]CACTCCTAAATAAGT	17420
rs29143952	snp	C/T	0.375	0.216506	intron-variant	Mnat1	Mm_Celera	12:73198126	CACTCCAGAAGAGGG[C/T]GTCAGATCTCATTAT	17420
rs29144096	snp	A/G	0.5	0	intron-variant	Mnat1	Mm_Celera	12:73261686	ATTTTTATAGTTTCC[A/G]TTGTTATATCTCCCT	17420
rs29144501	snp	A/C/T	0.375	0.216506	intron-variant	Mnat1	Mm_Celera	12:73160971	ATTAGTCTTTTTTTT[A/C/T]AACATGATTTAAAGT	17420
rs29144696	snp	C/G	0.5	0	intron-variant	Mnat1	Mm_Celera	12:73217574	ACCCTTCAGGTACAG[C/G]TGGTGCCCGCACCTC	17420
rs29145160	snp	C/G	0.375	0.216506	intron-variant	Mnat1	Mm_Celera	12:73186443	TATGAAAGGAAGGCA[C/G]TGAAGACTAGTCTTA	17420
rs29146099	snp	C/T	0.475309	0.108333	intron-variant	Mnat1	Mm_Celera	12:73236321	GCTAGAGTTTACGTC[C/T]TGACTCATAGCACTA	17420
rs29146405	snp	C/T	0.48	0.0979796	intron-variant	Mnat1	Mm_Celera	12:73126034	GCACTTGAGGCCATG[C/T]GCAGCTTTTTGTGTG	17420

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