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
rs31097134	snp	C/T	0.444444	0.157135	utr-variant-3-prime, downstream-variant-500B	Nosip	Mm_Celera	7:45078345	ATTAAAGGCGTGCGC[C/T]ACCACGCCCGGCTGT	66394
rs31153364	snp	C/G	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45071539	TTGGAGCTTTGCTTT[C/G]TTTGAAGAACACAGA	66394
rs31158750	snp	A/G	0.375	0.216506	intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45064318	CACCCCCAGTTCTTG[A/G]CAGTCTCTAAACTCG	66394
rs31179735	snp	C/T	0.444444	0.157135	intron-variant	Nosip	Mm_Celera	7:45069516	TTGTGAGCCACCATG[C/T]CAGTGCTGGAAGTTG	66394
rs31207243	snp	G/T	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45064811	TTGTTTTTGAGCAGG[G/T]TTTCTCTGTGCAGAC	66394
rs31237463	snp	A/C	0.277778	0.248452	intron-variant	Nosip	Mm_Celera	7:45066730	GCTTAGACTTACAGT[A/C]CCTCTGAGAAAATGA	66394
rs31336198	snp	C/T	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45070563	TCTGAGACAGGGTCT[C/T]TCTCAGTTCTTACTG	66394
rs31345396	snp	A/T	0.265928	0.249492	intron-variant	Nosip	Mm_Celera	7:45070778	AGAGGATTCCACCCC[A/T]TTGGGCCCTGCCTAC	66394
rs31377748	snp	C/G	0.5	0	intron-variant	Nosip	Mm_Celera	7:45067124	AGAGTCTTGGGGAAA[C/G]GGTGGTAAGGTGCTA	66394
rs31383397	snp	A/G	0.401235	0.199068	intron-variant	Nosip	Mm_Celera	7:45066880	CTCAAATAGGAAACA[A/G]ACTTTTTTTTTATAA	66394
rs31388296	snp	A/T	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45070120	GGGCATCAGATCCCA[A/T]TGCAGATGGTTATGA	66394
rs31432176	snp	A/T	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45066891	AACAAACTTTTTTTT[A/T]ATAATTTAAGTGACT	66394
rs31441324	snp	A/G	0.5	0	upstream-variant-2KB, intron-variant	Nosip, Prrg2	Mm_Celera	7:45061077	CTCTGCCTCCCAAGC[A/G]CTGGGATTAAAGGTG	66394
rs31486074	snp	A/G	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45070763	GATAGAGGGAGGGAG[A/G]GAGGATTCCACCCCT	66394
rs31525488	snp	A/G	0.444444	0.157135	intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45062954	TCTAGAACTCGCTAT[A/G]TAGTTAGCCTCAAAC	66394
rs31591839	snp	A/T	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45070043	TAAATCTTTTTTTTT[A/T]AAGATTTATTTATTT	66394
rs31598675	snp	C/G	0.375	0.216506	intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063660	GCACTGTCTACAGAG[C/G]CCAGAAGGCCATTAG	66394
rs31653574	snp	A/G	0.375	0.216506	intron-variant, missense	Nosip	Mm_Celera	7:45076237	AACACAGGTGACAAG[A/G]AATACCTGCCCTTGG	66394
rs31689137	snp	A/C	0.375	0.216506	synonymous-codon	Nosip	Mm_Celera	7:45077320	TCTCTAGGGCGGCAC[A/C]GGCTTTGCGGGCTCC	66394
rs31701846	snp	A/C	0.444444	0.157135	intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45062971	AGTTAGCCTCAAACT[A/C]ACAAAGATCCGCCAA	66394
rs31706287	snp	G/T	0.375	0.216506	utr-variant-3-prime	Nosip	Mm_Celera	7:45077838	ACCCTCATCCCTGCC[G/T]CCAAGTAAAAATAGC	66394
rs31711374	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063085	GTTTTTGTTTTTTGG[C/T]TTTTCGAGACAGGGT	66394
rs31730498	snp	C/T	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45075886	GGAGGAGGACTGGGT[C/T]CCATATTGAGTAGGA	66394
rs31760746	snp	A/G	0.265928	0.249492	intron-variant	Nosip	Mm_Celera	7:45070444	ATACATGTAGAGAGC[A/G]GACAATTCTTCCATG	66394
rs31762319	snp	A/G	0.265928	0.249492	utr-variant-3-prime	Nosip	Mm_Celera	7:45077524	CCAGGCAGAAACCCC[A/G]GCGTGAACCTGTGGG	66394
rs31769138	snp	C/T	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45064923	GGTGAAAGCTATGTA[C/T]CATGCCTGGCTGTAC	66394
rs31769310	snp	A/G	0.265928	0.249492	intron-variant	Nosip	Mm_Celera	7:45071413	AAATCAGGTTAAAAT[A/G]GGAACCAATGAAAAT	66394
rs31776630	snp	A/G	0.277778	0.248452	intron-variant	Nosip	Mm_Celera	7:45065912	AGTCACGTGTGGGGA[A/G]CAGGTTCCCTACCGT	66394
rs31783193	snp	A/G	0.375	0.216506	intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45064425	TTATGGCCTGTTTGC[A/G]GATGAACAGTCTGTT	66394
rs31815415	snp	A/T	0.255	0.24995	intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063855	TTTCTTGAGATGCAC[A/T]ACCTGGTACTGAAAT	66394
rs31840602	snp	C/T	0.265928	0.249492	intron-variant	Nosip	Mm_Celera	7:45071505	TGTATGTATGTGTTT[C/T]ACATGGGTAGTGACA	66394
rs31894656	snp	G/T	0.265928	0.249492	intron-variant	Nosip	Mm_Celera	7:45064979	CACCTTCCTAACTGA[G/T]CTGGGCCGCAGGCTT	66394
rs31901058	snp	C/T	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45069712	TTGGCACCAGGCACA[C/T]ATGTTGTGTATAGAC	66394
rs31935039	snp	A/G	0.255	0.24995	intron-variant	Nosip	Mm_Celera	7:45076435	GAAAAGCCGGTGAGG[A/G]CCCAATGTCCAGGAT	66394
rs32029051	snp	A/T	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45070234	TGGCTCCAAAGTTAA[A/T]TACACCGGGCTTGGT	66394
rs32058838	snp	A/G	0.32	0.24	intron-variant	Nosip	Mm_Celera	7:45076477	CAGTCCGTTCTCCCC[A/G]CCCCTCATGCCCCTT	66394
rs32076582	snp	A/G	0.387812	0.208586	intron-variant	Nosip	Mm_Celera	7:45066943	CTGTGAGTTGTGGCT[A/G]AAGCCCCTGCAGCTC	66394
rs32092666	snp	A/G	0.444444	0.157135	intron-variant	Nosip	Mm_Celera	7:45066784	AGTCCTGTCTTCGCA[A/G]CCCTTAGAAGGCTGA	66394
rs32101165	snp	A/G	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45067326	TGTGGCTCAGAGGCA[A/G]AGCCCCTAGAATCCT	66394
rs32156322	snp	G/T	0.387812	0.208586	intron-variant	Nosip	Mm_Celera	7:45066201	TTCTTCTCTCCTGTG[G/T]TGGTCTCCTCTGACT	66394
rs32176447	snp	A/G	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45070469	TCCATGGCACAGGAG[A/G]TTGAACTCAGGTTAT	66394
rs32203984	snp	G/T	0.32	0.24	utr-variant-3-prime	Nosip	Mm_Celera	7:45077387	ATGCAGGCCTGAGCC[G/T]TGGCCTAATAAACGT	66394
rs32233831	snp	C/T	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45070353	GAGGCCAGCCTAGCC[C/T]TTTTGAGACCTGTTG	66394
rs32279047	snp	A/G	0.255	0.24995	intron-variant	Nosip	Mm_Celera	7:45065859	GCTGGTTAGCTTTTG[A/G]TGGTAGACTGACAAT	66394
rs32295611	snp	C/T	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45069723	CACACATGTTGTGTA[C/T]AGACATCCATGCAGG	66394
rs32321721	snp	A/G	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45075935	CAGGGCCACCTTAGC[A/G]AAAGAACACGAAAGT	66394
rs32369475	snp	A/G	0.375	0.216506	upstream-variant-2KB, utr-variant-5-prime	Nosip, Prrg2	Mm_Celera	7:45062414	GCGACTAGGGGCAGA[A/G]TTATTTCCGGTCTCC	66394
rs32381615	snp	A/G	0.375	0.216506	utr-variant-3-prime	Nosip	Mm_Celera	7:45077479	TGCGGTGTGGGCCTG[A/G]GCTCCTGGGATTTAC	66394
rs32382775	snp	A/T	0.444444	0.157135	intron-variant	Nosip	Mm_Celera	7:45071232	GTGTGTGTGTGTGTG[A/T]GAGAGAGAGAGACAG	66394
rs32397927	snp	C/T	0.387812	0.208586	intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45062663	AGCGCTCTTGAACGC[C/T]TAGGTTGGAAGACGA	66394
rs32401407	snp	C/G	0.375	0.216506	utr-variant-3-prime	Nosip	Mm_Celera	7:45077839	CCCTCATCCCTGCCT[C/G]CAAGTAAAAATAGCT	66394
rs32440945	snp	C/T	0.375	0.216506	intron-variant	Nosip	Mm_Celera	7:45070369	TTTTGAGACCTGTTG[C/T]GGAAACCATTGGGTG	66394
rs32444111	snp	C/T	0.32	0.24	intron-variant	Nosip	Mm_Celera	7:45071647	ATGATTTGCCTTGTG[C/T]CCTAGCAGAGGTGTA	66394
rs36243007	snp	A/G	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45073632	TGGCTTTCTAATTCT[A/G]CCCTGTTGTCCTGTT	66394
rs36262509	snp	G/T	0.124444	0.216185	utr-variant-5-prime, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45062494	TTCCGGTTCGGGACG[G/T]AGTTGAAGCAACGAC	66394
rs36266967	snp	A/C	0.391111	0.206368	intron-variant	Nosip	Mm_Celera	7:45075971	CAACTGTTGCCAGTT[A/C]TGCCAGAGCTGCCCA	66394
rs36275742	snp	C/T	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45075313	GGCACCCGGGCTTCA[C/T]AGGCCAAGCACCTGC	66394
rs36301613	snp	C/T	0.244898	0.249948	intron-variant	Nosip	Mm_Celera	7:45074184	CAGGCAGCTCACCTC[C/T]ACCACAGGTGCAGTT	66394
rs36331368	snp	C/T	0.231111	0.249285	synonymous-codon	Nosip	Mm_Celera	7:45076173	GAAGGAGGCGGCCAT[C/T]GTGAGCCGGCCCCTC	66394
rs36351829	snp	C/T	0.231111	0.249285	intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45064291	CCACATTCTTTGCCA[C/T]TTAGTCTTTCTCACC	66394
rs36395487	snp	A/C	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45075146	CCTGTGCTTGGTCTT[A/C]CGCTGTACAATGGCC	66394
rs36428750	snp	A/G	0.124444	0.216185	intron-variant	Nosip	Mm_Celera	7:45068925	CCATGCCCGTGAAAC[A/G]GGAACTTCATCTTGA	66394
rs36429432	snp	A/T	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45067790	GAGGAGACATATAGG[A/T]GAGTGTGACTGTGGC	66394
rs36431943	snp	C/T	0.391111	0.206368	intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063315	TTAAGATTTATTAGC[C/T]GGGCAGTGGCAAAAA	66394
rs36480189	snp	A/G	0.124444	0.216185	intron-variant	Nosip	Mm_Celera	7:45066704	GTCATCACCACCACT[A/G]TGTTACCCAAGCTTA	66394
rs36508521	snp	C/G	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45068515	GTGGACATAAATTGA[C/G]TACACTCCGTAGATG	66394
rs36543664	snp	C/G	0.124444	0.216185	downstream-variant-500B	Nosip	Mm_Celera	7:45078704	CAGATGTCCACCTGC[C/G]GCCACTAGAGGGCAG	66394
rs36566831	snp	C/T	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45068846	TTTTATTTCTTGTTG[C/T]GCTCTGCTAGAATTC	66394
rs36624351	snp	A/C	0.244898	0.249948	downstream-variant-500B	Nosip	Mm_Celera	7:45078960	CACACAGGGACACAC[A/C]AAATACAGATGTTAC	66394
rs36643967	snp	C/T	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45067011	CCAGTCTCCATAGGC[C/T]TCTCTCTCAGTGGCA	66394
rs36646969	snp	A/T	0.391111	0.206368	intron-variant	Nosip	Mm_Celera	7:45066515	AATTATCCAGGTGGT[A/T]ACAGCTTGTTTTTTC	66394
rs36676612	snp	C/T	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45075492	ACCTCAGCTGGGTGA[C/T]CCAGGGAGTCTCCAG	66394
rs36680693	snp	A/G	0.260355	0.249785	intron-variant	Nosip	Mm_Celera	7:45076963	ACCGCAGCCCTCACC[A/G]CAGCCCGCACCCCAT	66394
rs36726102	snp	A/G	0.336735	0.234472	intron-variant	Nosip	Mm_Celera	7:45074443	AAAGAGAGGACTGAA[A/G]GGAGTGCTGTGAAGA	66394
rs36774951	snp	A/G	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45075185	GAAGCTAGAGGGTGC[A/G]CAGAGCAAGTGCAAG	66394
rs36778793	snp	C/T	0.391111	0.206368	intron-variant	Nosip	Mm_Celera	7:45070969	TCTCACTAAGTTACT[C/T]AGGCCAGGACACTAA	66394
rs36786690	snp	A/G	0.231111	0.249285	utr-variant-3-prime, downstream-variant-500B	Nosip	Mm_Celera	7:45078406	CACTGGCCATGCAGT[A/G]ATGAGAAGATGTGTT	66394
rs36801561	snp	A/G	0.391111	0.206368	intron-variant	Nosip	Mm_Celera	7:45067537	CACCACAAGTCAAGG[A/G]CACATCAATCAATTG	66394
rs37000550	snp	C/T	0.391111	0.206368	downstream-variant-500B	Nosip	Mm_Celera	7:45078597	TGGGTCTTTCCTGTG[C/T]GCGTAGTTTGCTGCT	66394
rs37004280	snp	A/T	0.391111	0.206368	intron-variant	Nosip	Mm_Celera	7:45066356	GCAACAGACCAAACC[A/T]CGGCTAGTTGGCTTC	66394
rs37082874	snp	A/G	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45068401	CTCAGTATTGAGTCT[A/G]TGTAAATGTACTGAA	66394
rs37125465	snp	A/G	0.391111	0.206368	intron-variant	Nosip	Mm_Celera	7:45074854	GGCAGGGCAGTTTCT[A/G]CAATGGTGGCGTCTG	66394
rs37162593	snp	A/G	0.260355	0.249785	intron-variant	Nosip	Mm_Celera	7:45073372	GACTGCTGTGGTTTA[A/G]GGCTGTGTTTTCGGC	66394
rs37179324	snp	A/G	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45077092	GTTGGCTCTTCTATG[A/G]CACTGTTTTCTTTCT	66394
rs37190410	snp	C/T	0.231111	0.249285	intron-variant	Nosip	GRCm38.p3	7:45071132	TGGAAGAGCAGTGAC[C/T]GCTGGAAGAGCAGTC	66394
rs37209184	snp	C/T	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45069865	CTGGAGGTGGCTAGC[C/T]CAGCTGGTCCTTGCT	66394
rs37233658	snp	C/T	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45076803	GGGGCTGACTTTTGG[C/T]ACTGTCTTCCACTGT	66394
rs37237238	snp	A/G	0.391111	0.206368	intron-variant	Nosip	Mm_Celera	7:45073070	TGCAGTTCCGCATGC[A/G]CACACTTGCCTAGCA	66394
rs37257687	snp	A/T	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45073404	ACCTGAACAGGCTTC[A/T]GGAGCAGGCTACTGA	66394
rs37296873	snp	A/G	0.231111	0.249285	downstream-variant-500B	Nosip	Mm_Celera	7:45078718	CGGCCACTAGAGGGC[A/G]GAACGTCACTGCCGA	66394
rs37318155	snp	C/T	0.231111	0.249285	downstream-variant-500B	Nosip	Mm_Celera	7:45078553	TTTCACTGCCCTTGT[C/T]GCACATTACCGGAGT	66394
rs37327208	snp	A/G	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45067761	GCCTCAACGTCCTGG[A/G]CAAAGGAGACCCTGA	66394
rs37387748	snp	A/G	0.391111	0.206368	intron-variant	Nosip	Mm_Celera	7:45075101	CCAGGCACTTAGCAG[A/G]GGCTTGAGATGTAAA	66394
rs37403962	snp	A/G	0.391111	0.206368	intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45063252	TTTTGAGGCAAGGTG[A/G]CATGTAGTCCAGGCT	66394
rs37460934	snp	C/T	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45069893	GCTTGGTGACAGTCA[C/T]AGGAAACCCTGTGGT	66394
rs37486489	snp	A/C	0.391111	0.206368	utr-variant-3-prime	Nosip	Mm_Celera	7:45077441	GCGCCTCATTGTAGG[A/C]CCGGCGACAGAAGGA	66394
rs37598419	snp	A/G	0.231111	0.249285	synonymous-codon	Nosip	Mm_Celera	7:45074034	CCGGGACGCTGTGAA[A/G]GACTTTGACTGCTGC	66394
rs37634098	snp	A/T	0.391111	0.206368	intron-variant, upstream-variant-2KB	Nosip, Prrg2	Mm_Celera	7:45062699	ATTTCCCAGGATGCC[A/T]TGTACTGTCTCCCTC	66394
rs37753649	snp	C/G	0.497778	0.0332592	intron-variant	Nosip	Mm_Celera	7:45074937	AGCATCCGCATAGAC[C/G]TCCTGCGGGCCAGGC	66394
rs37755133	snp	C/T	0.231111	0.249285	intron-variant	Nosip	Mm_Celera	7:45069291	GCCCTGAGTCACTCC[C/T]TTCCGTTGTTTGTTT	66394

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