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
rs3088589	snp	G/T	0.21875	0.248039	intron-variant	Nck2	GRCm38.p3	1:43492133	CAAGTGGGCAGCCAT[G/T]CGAGGCACCAGCTGA	17974
rs3655419	snp	A/G	0.489796	0.070696	intron-variant	Nck2	GRCm38.p3	1:43506408	CTCTTTTATCTGAAG[A/G]CTCAGTGCCTTAATC	17974
rs3662842	snp	A/G	0.5	0	intron-variant	Nck2	GRCm38.p3	1:43449466	AAAAACAAAACCCAC[A/G]AAATTCCTTTATGTC	17974
rs3664066	snp	A/C	0.5	0	intron-variant	Nck2	GRCm38.p3	1:43449691	TGCAGGTGTGTGCCT[A/C]GCTGGAGTGTTGGAG	17974
rs3703031	snp	G/T	0.471655	0.115624	intron-variant	Nck2	Mm_Celera	1:43467508	GTGTGATCAGCCGTA[G/T]TAGAACACACCCTGG	17974
rs3703581	snp	A/G	0.444444	0.157135	intron-variant	Nck2	Mm_Celera	1:43467580	GGCAGGAGGATCAGG[A/G]ATTCAAGGCCAGCCT	17974
rs3709917	snp	A/G	0.489796	0.070696	intron-variant	Nck2	GRCm38.p3	1:43480337	TTGGGGTCAGTCTCC[A/G]TCTGTTAGAAGGAAA	17974
rs3724978	snp	C/G	0.5	0	intron-variant	Nck2	GRCm38.p3	1:43480429	TAAAAAATACCTTAG[C/G]TAAACGGTTAGTCTT	17974
rs3724989	snp	C/T	0.5	0	intron-variant	Nck2	GRCm38.p3	1:43480434	AATACCTTAGCTAAA[C/T]GGTTAGTCTTGTCTG	17974
rs4136282	snp	A/C	0.5	0	intron-variant	Nck2	GRCm38.p3	1:43449602	GGGAATGGttttgtt[A/C]ttctgagacgtttcc	17974
rs6185575	snp	C/T	0.5	0	intron-variant	Nck2	GRCm38.p3	1:43454608	CTTCTGTTCTGACCA[C/T]CTCACCCTCTAAGCC	17974
rs6187198	snp	C/T	0.290657	0.246672	intron-variant	Nck2	Mm_Celera	1:43454898	ACACTGTTCTTCGGA[C/T]GACTCCCCTGCGCCC	17974
rs6286954	snp	A/G	0.32	0.24	intron-variant	Nck2	Mm_Celera	1:43472803	AGTAGCCTATGGTAT[A/G]GACCNTGTCTTTGGA	17974
rs6286960	snp	A/G	0.304688	0.243945	intron-variant	Nck2	Mm_Celera	1:43472808	CCTATGGTATNGACC[A/G]TGTCTTTGGAATCCA	17974
rs6287440	snp	A/G	0.5	0	intron-variant	Nck2	Mm_Celera	1:43472845	GGCAGCCTCAGATGG[A/G]AAAATCTNAGGACGN	17974
rs6287459	snp	C/T	0.359862	0.224567	intron-variant	Nck2	Mm_Celera	1:43472853	CAGATGGNAAAATCT[C/T]AGGACGNGGACAGTG	17974
rs6287475	snp	C/T	0.290657	0.246672	intron-variant	Nck2	Mm_Celera	1:43472860	NAAAATCTNAGGACG[C/T]GGACAGTGTAGTTAG	17974
rs6288037	snp	C/G	0.5	0	intron-variant	Nck2	Mm_Celera	1:43472975	GTAGCATTAATCACC[C/G]TGAGTTAGGTATTGT	17974
rs6288576	snp	C/T	0.359862	0.224567	intron-variant	Nck2	Mm_Celera	1:43473070	TGGGCATTTTAGGAC[C/T]GTGCTCTGGTGGGAG	17974
rs6288979	snp	A/T	0.290657	0.246672	intron-variant	Nck2	Mm_Celera	1:43473119	AGACGCCATGAAGGC[A/T]CTAAAGGATATCTGT	17974
rs6289117	snp	C/T	0.415225	0.187619	intron-variant	Nck2	Mm_Celera	1:43473194	GAAAGAAGTGTGGCC[C/T]AAGAAGATTTACATG	17974
rs6289603	snp	C/T	0.290657	0.246672	intron-variant	Nck2	Mm_Celera	1:43473258	TCATTACTACGTAGG[C/T]TCGTTTAGAAATAAA	17974
rs6289649	snp	A/G	0.290657	0.246672	intron-variant	Nck2	Mm_Celera	1:43473283	AATAAATACGCTGTC[A/G]TCTGGGTACTCATTT	17974
rs6289680	snp	C/G	0.290657	0.246672	intron-variant	Nck2	Mm_Celera	1:43473305	TACTCATTTGGTTTT[C/G]TGAAAAACTTGGTTT	17974
rs6290196	snp	A/G	0.5	0	intron-variant	Nck2	Mm_Celera	1:43473384	GTCTAACATTTATTC[A/G]TACGGGTGCGGCATG	17974
rs6392281	snp	C/T	0.359862	0.224567	intron-variant	Nck2	Mm_Celera	1:43458130	TTTGAATAAGCAGTG[C/T]TCACTTAGTGAGTAT	17974
rs6392318	snp	C/T	0.5	0	intron-variant	Nck2	GRCm38.p3	1:43458153	GTGAGTATTTATTGA[C/T]ACCAACTGTGTGCCA	17974
rs6392865	snp	C/T	0.359862	0.224567	intron-variant	Nck2	Mm_Celera	1:43458238	GAGATTTCTTTTAGT[C/T]CACACTCATTTCTGA	17974
rs6392945	snp	G/T	0.359862	0.224567	intron-variant	Nck2	Mm_Celera	1:43458278	ACCATCTCCACATTT[G/T]CGTGAGAGGTGACAC	17974
rs6393011	snp	A/G	0.5	0	intron-variant	Nck2	Mm_Celera	1:43458301	GGTGACACTACACAA[A/G]GTCTCTCCCACCCTC	17974
rs6407146	snp	C/T	0.290657	0.246672	intron-variant	Nck2	Mm_Celera	1:43458514	CAGACCATTTGTTTG[C/T]ACACAGTAGACTCTT	17974
rs6407260	snp	A/T	0.5	0	intron-variant	Nck2	Mm_Celera	1:43458590	GCTTGTCTGTTGCTT[A/T]CTTANTTAAAAAAAA	17974
rs6407263	snp	C/T	0.5	0	intron-variant	Nck2	Mm_Celera	1:43458595	TCTGTTGCTTNCTTA[C/T]TTAAAAAAAATCAGT	17974
rs6407702	snp	G/T	0.304688	0.243945	intron-variant	Nck2	Mm_Celera	1:43458632	ACTTATTGAAGGTTT[G/T]AGCTGAATATTGCAT	17974
rs6408261	snp	A/G	0.207612	0.24638	intron-variant	Nck2	Mm_Celera	1:43458735	TTGTTTTTATGTATG[A/G]Attttgagataggnt	17974
rs6408276	snp	C/T	0.5	0	intron-variant	Nck2	Mm_Celera	1:43458749	GNAttttgagatagg[C/T]tttcaggccctggct	17974
rs13475311	snp	G/T			synonymous-codon	Nck2	Mm_Celera	1:43554153	AGCGGACGAAGCTGC[G/T]GCTGAGGCCCCCAGC	17974
rs30510648	snp	C/T	0.33241	0.236027	intron-variant	Nck2	Mm_Celera	1:43463913	TTATTTTATAATGTT[C/T]TGGCAGTTGGATTGG	17974
rs30544951	snp	C/T	0.375	0.216506	intron-variant	Nck2	GRCm38.p3	1:43455757	TCTCCCTAGGATCTG[C/T]CTTGCTTGGCTTTAT	17974
rs30559195	snp	A/T	0.32	0.24	intron-variant	Nck2	GRCm38.p3	1:43456779	ATCAAAAGACATCAG[A/T]TTTCTTAGAAACTTT	17974
rs30570519	snp	A/G	0.375	0.216506	intron-variant	Nck2	GRCm38.p3	1:43452284	CTTCTTTAATGTTGT[A/G]TCTGGATACATTTGG	17974
rs30603448	snp	C/T	0.375	0.216506	intron-variant	Nck2	GRCm38.p3	1:43507441	GGAATGTGTGGAAAA[C/T]ACCAGCCCGAATCCA	17974
rs30604338	snp	C/T	0.444444	0.157135	intron-variant	Nck2	GRCm38.p3	1:43483252	TCTGCCACCCGCATC[C/T]CCTCGTGGGGCAGAC	17974
rs30612578	snp	A/G	0.487535	0.077957	intron-variant	Nck2	GRCm38.p3	1:43465759	TATGTGGCACAGTCG[A/G]TTCCATGAGCATCAG	17974
rs30654619	snp	C/G/T	0.375	0.216506	intron-variant	Nck2	GRCm38.p3	1:43507414	ACCTATTAGAAATGT[C/G/T]GGGGGTTGGGGAATG	17974
rs30665769	snp	A/G	0.33241	0.236027	intron-variant	Nck2	GRCm38.p3	1:43474549	CTCTATTCAGCTAGT[A/G]GTGGAGCAGGCTGCC	17974
rs30668834	snp	G/T	0.444444	0.157135	intron-variant	Nck2	GRCm38.p3	1:43483683	ATAGATTGAAGATTT[G/T]CAGGGTAACACAAAA	17974
rs30743927	snp	C/G	0.487535	0.077957	intron-variant	Nck2	GRCm38.p3	1:43461226	GGAGGCGATAGGGTG[C/G]TTCTTCAGCATATTT	17974
rs30759334	snp	A/T	0.456747	0.140554	intron-variant	Nck2	GRCm38.p3	1:43485740	TATTCAGGCACAAGA[A/T]GGAAGACAAACCACA	17974
rs30771005	snp	C/G	0.375	0.216506	intron-variant	Nck2	GRCm38.p3	1:43565451	AGTTGCCGTATCTCA[C/G]GCAGCCTTGCAGAGG	17974
rs30810517	snp	C/T	0.495	0.0497494	intron-variant	Nck2	GRCm38.p3	1:43482676	ATTGGATGAGTATCT[C/T]TCAGAAGGAAACAAG	17974
rs30849043	snp	A/G	0.444444	0.157135	intron-variant	Nck2	Mm_Celera	1:43454739	AAAAAAAAATCAATG[A/G]TAGGGAGTGGAGCTT	17974
rs30851620	snp	G/T	0.444444	0.157135	intron-variant	Nck2	GRCm38.p3	1:43500526	ACCCAGCCCACATCC[G/T]AAACTGACTGTTGTA	17974
rs30853989	snp	C/T	0.444444	0.157135	intron-variant	Nck2	GRCm38.p3	1:43483607	ACCAGTGGAACTTTC[C/T]AGAAAGTGAAGCCCT	17974
rs30859589	snp	C/T	0.375	0.216506	intron-variant	Nck2	GRCm38.p3	1:43475565	TTTTATAGCCTACCC[C/T]TTGGGGAGGGGCATC	17974
rs30898871	snp	C/G/T	0.484429	0.0868505	intron-variant	Nck2	GRCm38.p3	1:43507727	GTGCTGAGTTGTCTG[C/G/T]GCCAATTAGGTTGTA	17974
rs30901766	snp	A/C	0.475309	0.108333	intron-variant	Nck2	GRCm38.p3	1:43505174	ATAGTCTGTATGGGG[A/C]TGAACCTTTGAAAGG	17974
rs30908704	snp	A/G	0.487535	0.077957	intron-variant	Nck2	GRCm38.p3	1:43493051	GGAAACTAAATGGTT[A/G]TGTATCAGCTGTGTG	17974
rs30944904	snp	C/T	0.33241	0.236027	intron-variant	Nck2	GRCm38.p3	1:43474659	TTTGAAGTCATGCCA[C/T]AGCAACTCTTTGAGG	17974
rs30953163	snp	C/G	0.32	0.24	intron-variant	Nck2	GRCm38.p3	1:43448678	GTGCTGGGATTAAAG[C/G]CGTGCAACACCACGC	17974
rs30990828	snp	C/G	0.375	0.216506	intron-variant	Nck2	GRCm38.p3	1:43502652	CCAGTCAGCAGTACC[C/G]TTCTGTGGCCTGTGA	17974
rs31007990	snp	G/T	0.197531	0.244432	intron-variant	Nck2	GRCm38.p3	1:43469371	CTCCATCCTGCCCAC[G/T]GTCCTTGTGGACGGT	17974
rs31009436	snp	G/T	0.375	0.216506	upstream-variant-2KB	Nck2	Mm_Celera	1:43444187	CCACTGTCATCACGG[G/T]GGGAAGCTTGGTAGC	17974
rs31044463	snp	A/G	0.444444	0.157135	upstream-variant-2KB	Nck2	GRCm38.p3	1:43444338	TCTCCTCCAACAAGG[A/G]CATACCCTCCTAATC	17974
rs31056788	snp	C/T	0.493827	0.0552116	intron-variant	Nck2	GRCm38.p3	1:43459092	GATCACAAAGGTGGT[C/T]TGTGAAACTTTTCTA	17974
rs31130536	snp	A/C	0.493827	0.0552116	intron-variant	Nck2	GRCm38.p3	1:43534537	TGGTGTAAGTACAAT[A/C]TGGCAAGAGACTAGG	17974
rs31158552	snp	G/T	0.444444	0.157135	intron-variant	Nck2	GRCm38.p3	1:43461622	GAGGGCAGAGCGTAT[G/T]GTGGGGGATGCTATC	17974
rs31187945	snp	C/T	0.375	0.216506	intron-variant	Nck2	GRCm38.p3	1:43499741	TAGTTTTTTGTTTGT[C/T]TTGTTTTGTTGTTTT	17974
rs31226928	snp	C/T	0.444444	0.157135	intron-variant	Nck2	GRCm38.p3	1:43500525	AACCCAGCCCACATC[C/T]TAAACTGACTGTTGT	17974
rs31235948	snp	A/G	0.444444	0.157135	intron-variant	Nck2	GRCm38.p3	1:43483314	GTTCCCACAGTGGGC[A/G]CAGTAGCTGGTGGGA	17974
rs31240477	snp	A/T	0.5	0	intron-variant	Nck2	Mm_Celera	1:43503311	GCAACCTAAAAGTTT[A/T]TTTTTTTTTAATAGA	17974
rs31241631	snp	A/G	0.492188	0.0620098	intron-variant	Nck2	GRCm38.p3	1:43482814	AAGGTGAAGAAACTA[A/G]AGCTATTTTAAAAGT	17974
rs31286746	snp	A/C	0.408163	0.193609	intron-variant	Nck2	GRCm38.p3	1:43467780	CCCACAAGGCCAACA[A/C]ACTGTTTTTTTCGCT	17974
rs31297530	snp	A/G	0.375	0.216506	intron-variant	Nck2	GRCm38.p3	1:43467460	CAGTGCTTCGCAAAC[A/G]GCCCCTGGACTGAAT	17974
rs31305667	snp	A/G	0.495	0.0497494	intron-variant	Nck2	GRCm38.p3	1:43472197	AAAGGCTTTCTTCTT[A/G]ACAAGCTTTCATTCC	17974
rs31378057	snp	C/T	0.304688	0.243945	intron-variant	Nck2	Mm_Celera	1:43466939	TTCCATCCACAAACC[C/T]TGTGTCTGTGTTTAG	17974
rs31403525	snp	A/G	0.432133	0.171253	intron-variant	Nck2	Mm_Celera	1:43474887	GAAAGTAAGAGAGCC[A/G]CCTATAGCTGGAGCT	17974
rs31420911	snp	C/G	0.444444	0.157135	upstream-variant-2KB	Nck2	Mm_Celera	1:43444910	TTCTTTTTTTGTTAC[C/G]TAGGGTGAATTGTTT	17974
rs31490848	snp	A/G	0.495	0.0497494	intron-variant	Nck2	GRCm38.p3	1:43468861	AAGCAGTGGAGGCAA[A/G]ATCGAAAGACCCCCA	17974
rs31527127	snp	A/G	0.444444	0.157135	intron-variant	Nck2	GRCm38.p3	1:43510213	TCCCTAATTTACTGA[A/G]CTCCATTAAATTTAA	17974
rs31549145	snp	C/T	0.375	0.216506	intron-variant	Nck2	GRCm38.p3	1:43448850	TCCCGCCCTTTCTTT[C/T]CCCTGGAGTTCACTT	17974
rs31552064	snp	C/T	0.475309	0.108333	intron-variant	Nck2	GRCm38.p3	1:43502913	AGTTTACTTTCTAAC[C/T]CGGTTTTAAGCTCAG	17974
rs31569915	snp	A/C	0.429688	0.173817	intron-variant	Nck2	GRCm38.p3	1:43482824	AACTAAAGCTATTTT[A/C]AAAGTAGCCCAAGAT	17974
rs31620260	snp	C/G	0.32	0.24	intron-variant	Nck2	GRCm38.p3	1:43448696	TGCAACACCACGCCC[C/G]GCAATGCATTTCTTT	17974
rs31622177	snp	A/G	0.375	0.216506	intron-variant	Nck2	Mm_Celera	1:43454435	CCCCCCCCTCTACGC[A/G]AGACCAGACATTGTA	17974
rs31652254	snp	A/G	0.497778	0.0332592	intron-variant	Nck2	GRCm38.p3	1:43487116	ATATACTATTCCAGG[A/G]TCTATTGGACCAAAT	17974
rs31676158	snp	A/G	0.444444	0.157135	intron-variant	Nck2	GRCm38.p3	1:43483381	GTTTGTTCCTTTGAG[A/G]ATTATAAAATATGCA	17974
rs31734176	snp	G/T	0.375	0.216506	intron-variant	Nck2	GRCm38.p3	1:43483933	CTTCTGTAGAAGTAG[G/T]TTCCAACTGATGTGC	17974
rs31767678	snp	C/T	0.375	0.216506	intron-variant	Nck2	GRCm38.p3	1:43455758	CTCCCTAGGATCTGC[C/T]TTGCTTGGCTTTATA	17974
rs31835972	snp	C/T	0.475309	0.108333	intron-variant	Nck2	GRCm38.p3	1:43466810	AAGCCTGCTGTCCTT[C/T]AACTCCTTCCATGTG	17974
rs31865475	snp	A/G	0.495	0.0497494	intron-variant	Nck2	GRCm38.p3	1:43458439	GTAGCTGTGTACGTT[A/G]GTGGCTGCCTCAACA	17974
rs31867299	snp	G/T	0.487535	0.077957	intron-variant	Nck2	GRCm38.p3	1:43456620	ATCCGTGTCCAGTCA[G/T]CATACCTGTACCACA	17974
rs31873204	snp	A/G	0.487535	0.077957	intron-variant	Nck2	GRCm38.p3	1:43475442	TTGGCACCTAGTAAC[A/G]CCATCACTGTCTGGC	17974
rs31887674	snp	C/G	0.375	0.216506	intron-variant	Nck2	GRCm38.p3	1:43467453	TGTAGAACAGTGCTT[C/G]GCAAACGGCCCCTGG	17974
rs31894678	snp	G/T	0.49827	0.0293608	intron-variant	Nck2	GRCm38.p3	1:43503662	GCCTCATGCAGGCCA[G/T]TCATTCTGTTCATAG	17974
rs31902252	snp	A/G	0.498615	0.0262793	intron-variant	Nck2	GRCm38.p3	1:43565443	GTTGAGTCAGTTGCC[A/G]TATCTCAGGCAGCCT	17974
rs31919412	snp	A/C/G	0.32	0.24	intron-variant	Nck2	GRCm38.p3	1:43484123	CCTCAGTCCCCTTTG[A/C/G]GAAATGCCAGCCTTA	17974
rs31929637	snp	A/G	0.49827	0.0293608	intron-variant	Nck2	GRCm38.p3	1:43564916	ATAATAATGAATTCT[A/G]TGACCCTGTTGTCTA	17974
rs31955630	snp	A/G	0.432133	0.171253	intron-variant	Nck2	GRCm38.p3	1:43485050	GAACCATAATTCTTA[A/G]TAAGTGCTAGGTCTT	17974
rs31985789	snp	A/G	0.487535	0.077957	intron-variant	Nck2	GRCm38.p3	1:43467739	TCGTGGTAGTGTAGT[A/G]GGATTGAGTAATTGT	17974

Full records

It may take some time, please wait.