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
rs13459320	snp	A/G	0.493827	0.0552116	synonymous-codon	Stambp	Mm_Celera	6:83564187	TGAGAAGAAAGATGC[A/G]GTCAAGGTGGGTCCT	70527
rs13478863	snp	C/T	0.46875	0.121031	intron-variant	Stambp	GRCm38.p3	6:83556021	GGCCTCTATAGCCTG[C/T]CCACAAACATTCTAG	70527
rs29831645	snp	C/T	0.391111	0.206368	upstream-variant-2KB, intron-variant	Stambp, Gm21284	Mm_Celera	6:83573952	CATCTCTCTCCCCAG[C/T]GCCTACCATGACTTT	70527
rs29873401	snp	C/T	0.444444	0.157135	intron-variant	Stambp	Mm_Celera	6:83559002	CCTTCTTGAGTTCTT[C/T]GTATATATTGGATAT	70527
rs29916384	snp	C/T	0.48	0.0979796	intron-variant, upstream-variant-2KB	Stambp, Gm21284	Mm_Celera	6:83567343	TTTTTAACTTGAATT[C/T]CTCCCTTCTAATGTC	70527
rs29965665	snp	A/G	0.375	0.216506	intron-variant	Stambp	Mm_Celera	6:83547988	TCTTCTTTTTTTGCC[A/G]GGCGGTGGTGGCACA	70527
rs30015616	snp	A/C	0.375	0.216506	intron-variant, upstream-variant-2KB	Stambp, Gm21284	Mm_Celera	6:83567573	ATATGGGTGATGGTT[A/C]ACTTTCGGAAGGAGG	70527
rs30018316	snp	C/T	0.456747	0.140554	intron-variant	Stambp	GRCm38.p3	6:83556444	AGCAGGTTAGAGTTC[C/T]GTGGGCTCTCAGCCC	70527
rs30018917	snp	C/G	0.375	0.216506	upstream-variant-2KB, intron-variant	Stambp, Gm21284	Mm_Celera	6:83574165	AAGGCACTGAGATGG[C/G]GTGCACTCATGAAGT	70527
rs30070828	snp	C/T	0.5	0	intron-variant	Stambp, LOC105242698	GRCm38.p3	6:83545746	ATGCCTGCTGTTATA[C/T]AGTGAGCCCTATACT	70527
rs30074809	snp	A/G	0.444444	0.157135	intron-variant, upstream-variant-2KB	Stambp, Gm21284	Mm_Celera	6:83566104	GCTTCGAGGTCGGCT[A/G]GTGCCTGCCGTAAGC	70527
rs30114247	snp	C/T	0.444444	0.157135	intron-variant	Stambp	GRCm38.p3	6:83556180	GTGTGCAGGGACAAA[C/T]GACTGGGAGAGGTTT	70527
rs30118638	snp	A/G	0.493827	0.0552116	intron-variant	Stambp	Mm_Celera	6:83556133	TAAAAGCTCTCGGTG[A/G]TACTCTGAGTTGATA	70527
rs30131762	snp	G/T	0.444444	0.157135	intron-variant	Stambp	Mm_Celera	6:83559523	GAGAATGAGGAACAC[G/T]CCTCCACTGTTGGTG	70527
rs30163795	snp	A/C	0.444444	0.157135	intron-variant	Stambp, LOC105242698	GRCm38.p3	6:83544175	TCCATCTTTCTGGTG[A/C]CACCTCTGAGTGTTG	70527
rs30169848	snp	C/T	0.375	0.216506	intron-variant	Stambp	Mm_Celera	6:83565527	GGGTAAAACCCCATG[C/T]TGTGCAAGCCTGCTG	70527
rs30225946	snp	A/G	0.493827	0.0552116	intron-variant	Stambp	GRCm38.p3	6:83557325	ATTGCCCCTGGGATC[A/G]TGCCATGCACTCTCT	70527
rs30264624	snp	A/G	0.33241	0.236027	intron-variant	Stambp	Mm_Celera	6:83562372	ATTCATGCTTTGTTC[A/G]ATACCTCTTAAAGCC	70527
rs30273175	snp	A/G	0.444444	0.157135	intron-variant	Stambp	Mm_Celera	6:83561096	AAAGAAAAGAAAAGA[A/G]AAGAAGAAAGGAAAG	70527
rs30316731	snp	C/G	0.48	0.0979796	intron-variant, upstream-variant-2KB	Stambp, Gm21284	Mm_Celera	6:83567290	TGACAAGTACTTTAC[C/G]CATAAGACATCTCTC	70527
rs30360930	snp	C/T	0.444444	0.157135	intron-variant	Stambp	GRCm38.p3	6:83558323	AAAGCCAAACTGCCC[C/T]ACAAGAAGATACAGT	70527
rs30369301	snp	G/T	0.444444	0.157135	intron-variant	Stambp	Mm_Celera	6:83559048	TGCAGGATTAGTAAA[G/T]ATCTTTTCCCAATCT	70527
rs30377451	snp	C/T	0.375	0.216506	upstream-variant-2KB, intron-variant	Stambp, Gm21284	Mm_Celera	6:83574107	TGATCGTTTTGTTCT[C/T]GGAACCAAATCTTCT	70527
rs30414228	snp	A/G	0.375	0.216506	intron-variant	Stambp	Mm_Celera	6:83548074	CCAGCCTGGTCTACA[A/G]AGTGAGTTCCAGGAC	70527
rs30415394	snp	A/G	0.408163	0.193609	intron-variant	Stambp	GRCm38.p3	6:83556145	GTGGTACTCTGAGTT[A/G]ATACGAGAGCACTAG	70527
rs30474678	snp	C/T	0.35503	0.226867	intron-variant	Stambp	Mm_Celera	6:83556162	TACGAGAGCACTAGT[C/T]GTGTGTGCAGGGACA	70527
rs30509548	snp	A/G	0.391111	0.206368	intron-variant	Stambp, Gm21284	Mm_Celera	6:83570059	ACCACTGGGACATGC[A/G]GTCTCAGCCTGAGAA	70527
rs30568600	snp	C/T	0.5	0	intron-variant	Stambp, Gm21284	Mm_Celera	6:83568976	TGCTGGGATGAAAGG[C/T]GTGCGCCACCACTGC	70527
rs30646611	snp	A/G/T	0.444444	0.157135	intron-variant	Stambp	GRCm38.p3	6:83556855	CTTGCCTTCCTCCCC[A/G/T]GCCCTACATCTCTAG	70527
rs30662645	snp	C/T	0.375	0.216506	intron-variant	Stambp	Mm_Celera	6:83562342	GAGCCATCTCTCCAG[C/T]CCCCCCAATCCAGAA	70527
rs30694402	snp	A/G	0.231111	0.249285	upstream-variant-2KB, intron-variant	Stambp, Gm21284	Mm_Celera	6:83574438	GGGACTGAAAAAGAC[A/G]AAAAGGTAGATAGAC	70527
rs30711197	snp	A/C	0.336735	0.234472	upstream-variant-2KB, intron-variant	Stambp, Gm21284	Mm_Celera	6:83574232	GGACAGCAAGGAGGA[A/C]AGGCTGCAGGTGTGA	70527
rs30804898	snp	C/G	0.5	0	upstream-variant-2KB, intron-variant	Stambp, Gm21284	Mm_Celera	6:83573591	GGTCATGAACAGCAG[C/G]ATGGAAGTGTAAGCC	70527
rs30807610	snp	A/G	0.5	0	intron-variant	Stambp, Gm21284	Mm_Celera	6:83569049	GAATCTAGACACTCA[A/G]GTTTGCCAAAGCTAA	70527
rs30852475	snp	A/G	0.493827	0.0552116	intron-variant	Stambp	GRCm38.p3	6:83553839	AGGCCCTCTAGTCTT[A/G]CATGCTTAGTTCTTC	70527
rs30853031	snp	A/C	0.415225	0.187619	intron-variant	Stambp	Mm_Celera	6:83561051	TACTTGATGATTAAA[A/C]AAAGAAAGAAGAGAA	70527
rs30854977	snp	C/T	0.493827	0.0552116	downstream-variant-500B, intron-variant	Stambp, LOC105242698	GRCm38.p3	6:83542813	TATCCACTCTTCTCT[C/T]ATGTTAGTGCCACAG	70527
rs30857225	snp	C/T	0.231111	0.249285	missense, intron-variant	Stambp, Gm21284	Mm_Celera	6:83570361	CTTCTTCCGAGTAAA[C/T]GGACGCCATGCGGAT	70527
rs30904756	snp	A/G	0.391111	0.206368	intron-variant	Gm21284, Stambp	Mm_Celera	6:83574555	TGTACGATTGCAGGC[A/G]CATTTCATACCTGAT	70527
rs30904981	snp	A/G	0.375	0.216506	intron-variant	Stambp	Mm_Celera	6:83548005	GCGGTGGTGGCACAC[A/G]CCTTTAATCCCAGCA	70527
rs30909497	snp	C/G	0.391111	0.206368	upstream-variant-2KB, intron-variant	Stambp, Gm21284	Mm_Celera	6:83574267	CAGCAGGAGAAAACC[C/G]GCCAGGCTGGGCTGT	70527
rs30940287	snp	A/G	0.375	0.216506	intron-variant, upstream-variant-2KB	Stambp, Gm21284	Mm_Celera	6:83566608	CATCCAGAGGACCTG[A/G]GATAGATTCCCAACA	70527
rs30954533	snp	A/C	0.375	0.216506	intron-variant, upstream-variant-2KB	Stambp, Gm21284	Mm_Celera	6:83566731	ACATACATGCATGAA[A/C]CCCCCCCACACACAC	70527
rs30999137	snp	C/T	0.444444	0.157135	intron-variant	Stambp	Mm_Celera	6:83559528	TGAGGAACACGCCTC[C/T]ACTGTTGGTGGGATT	70527
rs36240107	snp	A/C	0.391111	0.206368	intron-variant	Stambp	Mm_Celera	6:83547879	TTTGAGACAGCTTTC[A/C]CAGTACTCTGGCTTA	70527
rs36242031	snp	A/G	0.336735	0.234472	intron-variant	Stambp	Mm_Celera	6:83564123	CTGCAGTTGCATGTC[A/G]GTTACTCGGAGATGC	70527
rs36242574	snp	C/T	0.336735	0.234472	intron-variant	Stambp	Mm_Celera	6:83563630	TGTCTGTCCCCAGGT[C/T]GCCCTCTTGGACACC	70527
rs36242879	snp	G/T	0.497041	0.0383476	intron-variant	Stambp	GRCm38.p3	6:83555833	AGAAAGTACTCTTTA[G/T]GGAAGCAGCTGCGTT	70527
rs36251149	snp	A/G	0.124444	0.216185	intron-variant, downstream-variant-500B	Stambp, LOC105242698	Mm_Celera	6:83547227	TTTCCACATAGATAC[A/G]TACACAGAACAGCGG	70527
rs36276462	snp	A/G	0.32	0.24	intron-variant	Stambp	Mm_Celera	6:83561159	GCGGTTCGTGGAGGA[A/G]ACTTCAGAGGGAACA	70527
rs36279680	snp	C/T	0.260355	0.249785	intron-variant	Stambp	Mm_Celera	6:83558010	CGGCTCTCGGAATCT[C/T]GTTGTTCAGGCTATT	70527
rs36286382	snp	A/G	0.231111	0.249285	intron-variant	Stambp	Mm_Celera	6:83551519	CACGTTTACCAGGAC[A/G]TGGAGCTTAAAGGAA	70527
rs36288693	snp	A/C	0.497778	0.0332592	intron-variant	Stambp	GRCm38.p3	6:83555012	AGCTTCCAACTCTAG[A/C]AGGCACTCTCAGTCT	70527
rs36290752	snp	A/G	0.32	0.24	intron-variant	Stambp	Mm_Celera	6:83554232	CAGAGGGCTTTGTGC[A/G]TTCTCCTTATACAAG	70527
rs36299589	snp	G/T	0.497778	0.0332592	intron-variant	Stambp	GRCm38.p3	6:83555475	TCTGAAACCCGAAGT[G/T]TCCTCTGTTCATCTG	70527
rs36300535	snp	C/T	0.396694	0.202437	intron-variant, utr-variant-5-prime	Gm21284, Stambp	Mm_Celera	6:83575757	TTCTCCTGCATCTGC[C/T]TCCTACGGGCTAGGA	70527
rs36305951	snp	A/C/G	0.297521	0.245442	intron-variant, utr-variant-5-prime	Gm21284, Stambp	Mm_Celera	6:83574571	CATTTCATACCTGAT[A/C/G]CTTATCTCCAGCTAG	70527
rs36316999	snp	C/G	0.297521	0.245442	intron-variant	Stambp, Gm21284	Mm_Celera	6:83571000	acaaaagaaaacCAA[C/G]CTTGTCCTGCAATTT	70527
rs36318839	snp	A/G	0.391111	0.206368	missense	Stambp	GRCm38.p3	6:83561762	CTGTGTTACAGTCTG[A/G]AGTCTGCGTGGGCGA	70527
rs36323685	snp	A/G	0.444444	0.157135	utr-variant-3-prime, intron-variant	Stambp, LOC105242698	GRCm38.p3	6:83543502	TGGATCTAGAGAAGT[A/G]TTTTCTCTTGCATCC	70527
rs36333188	snp	A/G	0.32	0.24	utr-variant-3-prime, intron-variant	Stambp, LOC105242698	GRCm38.p3	6:83543469	GGTAAATTTCAAGAG[A/G]AACAGAAGGCCAGTG	70527
rs36334465	snp	C/T	0.124444	0.216185	intron-variant	Stambp, LOC105242698	Mm_Celera	6:83546551	TCATATTTTATGGGG[C/T]GTGGCTCTGGTTCCT	70527
rs36340921	snp	C/T	0.32	0.24	utr-variant-3-prime, intron-variant	Stambp, LOC105242698	GRCm38.p3	6:83543296	TTTAAACAAGATCCA[C/T]GTATGGGGGCTGTGA	70527
rs36342407	snp	A/G	0.32	0.24	intron-variant	Stambp	Mm_Celera	6:83554247	ATTCTCCTTATACAA[A/G]CACGAGTCCCACTGT	70527
rs36355556	snp	C/T	0.42	0.183303	intron-variant	Stambp	Mm_Celera	6:83555203	ACTTTTGCTCTTTAG[C/T]AGCCCCTCTCTCCAG	70527
rs36381827	snp	C/T	0.165289	0.235211	intron-variant	Stambp	Mm_Celera	6:83565659	CTACAACAATAACGA[C/T]GACTACTACTACCAA	70527
rs36395317	snp	A/G	0.244898	0.249948	downstream-variant-500B, intron-variant	Stambp, LOC105242698	Mm_Celera	6:83543121	AATTATAAGTGAAGT[A/G]GAACACAGTTCAGTG	70527
rs36424738	snp	C/T	0.497778	0.0332592	intron-variant	Stambp	GRCm38.p3	6:83554618	CTTAATGATTCAGTG[C/T]GCTGCACCATTAGTC	70527
rs36427083	snp	C/T	0.32	0.24	intron-variant	Stambp	Mm_Celera	6:83552934	TTTATTTTGCCTGGG[C/T]TGGGTCCCTCATCTC	70527
rs36472326	snp	A/C	0.124444	0.216185	intron-variant	Stambp	Mm_Celera	6:83558511	CGGATCAAGGCCTGG[A/C]ACAAACAAATAGCCC	70527
rs36476104	snp	A/G	0.165289	0.235211	intron-variant	Gm21284, Stambp	Mm_Celera	6:83575111	TCAGGGAACAGTGTG[A/G]TCTAGTGTTCTTATC	70527
rs36484520	snp	A/G	0.486111	0.0821678	intron-variant	Stambp	GRCm38.p3	6:83554306	CACATTACCTTGCCC[A/G]GCCTGCCGCCTTTTC	70527
rs36484982	snp	C/T	0.152778	0.230321	intron-variant, upstream-variant-2KB	Stambp, Gm21284	Mm_Celera	6:83566948	GTTGAGAAGGCTCCA[C/T]TTATCACTAAAAGAA	70527
rs36493880	snp	G/T	0.32	0.24	intron-variant	Stambp	Mm_Celera	6:83556815	GCAGCATCAAGGAAT[G/T]GGTTCAAGCCTTCCC	70527
rs36520360	snp	G/T	0.46875	0.121031	intron-variant	Stambp, Gm21284	Mm_Celera	6:83569244	TGGTATGACTGATGT[G/T]CGTGTGTCTGTCTGG	70527
rs36555379	snp	A/G	0.32	0.24	intron-variant	Stambp	Mm_Celera	6:83556643	CAGGCTGGGCCAATG[A/G]CATAACCCTAGGGTC	70527
rs36557356	snp	C/T	0.391111	0.206368	intron-variant	Stambp	Mm_Celera	6:83563688	ATCCCTACTGGTTGG[C/T]GACTCTTTTGAGGCA	70527
rs36561727	snp	C/T	0.132653	0.220748	intron-variant	Stambp	Mm_Celera	6:83557702	TGAGTCCCAGGGTTC[C/T]GGGCTCCGTAGGGAT	70527
rs36578509	snp	A/G	0.165289	0.235211	intron-variant, upstream-variant-2KB	Gm21284, Stambp	Mm_Celera	6:83575824	CAGCTCCTGGCTGCC[A/G]CTGGCATGGCAGTTA	70527
rs36604686	snp	C/T	0.497778	0.0332592	intron-variant	Stambp	GRCm38.p3	6:83554814	CATCCCTATGGTTCG[C/T]GCCAGGACTTCCTGT	70527
rs36609527	snp	C/T	0.142012	0.225474	downstream-variant-500B, intron-variant	Stambp, LOC105242698	Mm_Celera	6:83543004	TGAAGGTTGTCAGGC[C/T]TAAGGAGAAAGTGGG	70527
rs36617376	snp	C/T	0.42	0.183303	intron-variant	Stambp	Mm_Celera	6:83555219	AGCCCCTCTCTCCAG[C/T]GGCCAGTGAATCACT	70527
rs36643451	snp	C/T	0.391111	0.206368	intron-variant	Stambp	Mm_Celera	6:83553026	AGCAAGGCAGAATCA[C/T]GAATGACTGGGATGA	70527
rs36656227	snp	A/G	0.244898	0.249948	intron-variant	Stambp	Mm_Celera	6:83554292	GTGCTGCCTTAAGCC[A/G]CATTACCTTGCCCGG	70527
rs36657533	snp	A/G	0.32	0.24	intron-variant, nc-transcript-variant	Stambp, LOC105242698	Mm_Celera	6:83547199	GACCTGAGGAGCTTC[A/G]TGTGCTTGCTGGTTT	70527
rs36701316	snp	A/G	0.165289	0.235211	intron-variant	Stambp	Mm_Celera	6:83564840	TCCTATGCCCAAAGT[A/G]TAACTCTGAAAAGTG	70527
rs36709254	snp	C/T	0.124444	0.216185	nc-transcript-variant, upstream-variant-2KB	Gm21284, Stambp	Mm_Celera	6:83576101	TCCATAGCAAGAGAG[C/T]CCAGAAATGGTCATG	70527
rs36709435	snp	C/T	0.32	0.24	intron-variant	Stambp	Mm_Celera	6:83552101	CAGTGATCTAGTTGC[C/T]GTGCTGGCCCACTGA	70527
rs36747189	snp	A/T	0.32	0.24	intron-variant	Stambp	Mm_Celera	6:83554995	ATTAATACTTGGCAG[A/T]GAGCTTCCAACTCTA	70527
rs36748642	snp	A/G	0.32	0.24	intron-variant	Gm21284, Stambp	Mm_Celera	6:83574783	TTGTTAAAAAAAAAA[A/G]AATGCTTAAGCCAGA	70527
rs36754173	snp	A/G	0.32	0.24	intron-variant	Stambp	Mm_Celera	6:83563799	CGGGGCTGGCTAGGT[A/G]GCACACGTGCTCTGC	70527
rs36754740	snp	C/T	0.391111	0.206368	intron-variant	Stambp	Mm_Celera	6:83558777	AAGCTAACAGTGCGG[C/T]GCGGTGGGTAAGACA	70527
rs36762963	snp	G/T	0.489796	0.070696	intron-variant	Stambp	Mm_Celera	6:83555281	GCCGCCAGATAGCGC[G/T]CTCTCTCTCTTTGAC	70527
rs36776794	snp	A/G	0.32	0.24	intron-variant	Stambp, LOC105242698	Mm_Celera	6:83546832	GAGACTTAGTAACTG[A/G]CGGAGAACGTTTGCC	70527
rs36841586	snp	A/G	0.48	0.0979796	intron-variant, upstream-variant-2KB	Gm21284, Stambp	Mm_Celera	6:83577713	AGCACAGACCAGTTT[A/G]ACCTGATGGACTTTA	70527
rs36849681	snp	C/T	0.32	0.24	intron-variant	Stambp, LOC105242698	Mm_Celera	6:83546230	ACAATGCTGGCTCAA[C/T]GTCAGTGGCCTGACC	70527
rs36851004	snp	A/C	0.426035	0.177515	intron-variant	Stambp	GRCm38.p3	6:83555869	GCCTTGAAGATCATC[A/C]TCAAAGCATTCAATG	70527
rs36878879	snp	G/T	0.336735	0.234472	intron-variant	Stambp	Mm_Celera	6:83555843	CTTTAGGGAAGCAGC[G/T]GCGTTGCCTTGCCTT	70527
rs36896010	snp	C/T	0.391111	0.206368	intron-variant	Stambp	Mm_Celera	6:83558405	AGCAAGAGCCATACA[C/T]GAATTCCACAGAGAA	70527
rs36906403	snp	A/G	0.32	0.24	intron-variant	Stambp	Mm_Celera	6:83553012	ATGTTCACCCCAGCA[A/G]CAAGGCAGAATCATG	70527

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