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
rs3674858	snp	C/G	0.495868	0.0452663	intron-variant	Nod2	GRCm38.p3	8:88654038	TGGACAGAAAAGTAT[C/G]GCTGTGTATGTCTGA	257632
rs3674878	snp	C/G	0.5	0	intron-variant	Nod2	GRCm38.p3	8:88654048	AGTATGGCTGTGTAT[C/G]TCTGAAACTTATATT	257632
rs3700029	snp	A/G	0.5	0	intron-variant	Nod2	GRCm38.p3	8:88658528	acctatctgtccatc[A/G]tccatccatctgccc	257632
rs3700594	snp	C/T	0.5	0	intron-variant	Nod2	GRCm38.p3	8:88658623	TACTGCCTCTGTCAT[C/T]GGGACTAAATCAGTG	257632
rs3700655	snp	A/G	0.5	0	intron-variant	Nod2	GRCm38.p3	8:88658662	AGAAAACTTTGTTGT[A/G]ATGTTCATACCTCAG	257632
rs3701099	snp	A/G	0.5	0	intron-variant	Nod2	GRCm38.p3	8:88658682	TCATACCTCAGCTGG[A/G]GATAGATCATAGCAG	257632
rs3701243	snp	C/G	0.5	0	intron-variant	Nod2	GRCm38.p3	8:88658751	TGGAAGATTAATAAA[C/G]GAGTGGATCTGTCTG	257632
rs3701800	snp	A/G	0.5	0	intron-variant	Nod2	GRCm38.p3	8:88658812	TTCACCTTCCTGAAA[A/G]GTTGTTAGAGTATTC	257632
rs4136007	snp	C/T	0.5	0	intron-variant	Nod2	GRCm38.p3	8:88658554	tgcccatccatccat[C/T]catccatccatccat	257632
rs6155594	snp	A/G	0.359862	0.224567	intron-variant	Nod2	Mm_Celera	8:88653488	CCGTGGCAGCCCAGA[A/G]CTTGGCCTCAGTTGC	257632
rs13479904	snp	A/G	0.393491	0.20472	missense	Nod2	GRCm38.p3	8:88663745	AGGACCATGGTGTTG[A/G]CTCAGTCTCGCTTCC	257632
rs32536897	snp	A/C	0.5	0	intron-variant	Nod2	GRCm38.p3	8:88661294	ATATAACTGGGAAGA[A/C]ACCTAATATAGACTT	257632
rs32572980	snp	A/T	0.5	0	intron-variant	Nod2	Mm_Celera	8:88678995	TTTTTTTTTTTTTTT[A/T]ACTGAAGGTTGGACT	257632
rs32574918	snp	C/G	0.432133	0.171253	intron-variant	Nod2	GRCm38.p3	8:88674287	GAGCTCTTGCTAACA[C/G]CCGCAGGGGCAGGCT	257632
rs32577206	snp	C/T	0.432133	0.171253	intron-variant	Nod2	GRCm38.p3	8:88647985	CACCCACGGTTGATA[C/T]CCTGCAGGGGAAATG	257632
rs32581751	snp	A/G	0.444444	0.157135	intron-variant	Nod2	GRCm38.p3	8:88655629	GGGACTGAGGTAGCA[A/G]TGTGAGCTCTGACTT	257632
rs32583224	snp	C/T	0.277778	0.248452	intron-variant	Nod2	Mm_Celera	8:88673758	GATTGGGTGGCTTTA[C/T]GTAATCTATTTGACA	257632
rs32584185	snp	A/C	0.432133	0.171253	intron-variant	Nod2	GRCm38.p3	8:88679320	TTCCTCTAAACCTTT[A/C]ACTGTTTTCAGGGGA	257632
rs32595398	snp	G/T	0.432133	0.171253	intron-variant	Nod2	GRCm38.p3	8:88675069	AGTTCATTGAACTTT[G/T]TGTATGCACTCCATT	257632
rs32600928	snp	A/C	0.48	0.0979796	intron-variant	Nod2	GRCm38.p3	8:88680056	CTGGTCTGGTTTCAG[A/C]ACCTTCTTTGTAGTT	257632
rs32602113	snp	C/G	0.401235	0.199068	upstream-variant-2KB	Nod2	GRCm38.p3	8:88647220	ACTGCAGGCAGGCCT[C/G]TTCCCGGATACCTGT	257632
rs32608202	snp	C/T	0.401235	0.199068	intron-variant	Nod2	GRCm38.p3	8:88675362	CTTCATTTGCTTGTC[C/T]GTCACTCGCCCTTCA	257632
rs32613962	snp	C/G	0.444444	0.157135	intron-variant	Nod2	GRCm38.p3	8:88673408	CTTTTATGGTTTTTC[C/G]AGACAGAGTTTCTCT	257632
rs32619247	snp	A/G	0.475309	0.108333	intron-variant	Nod2	GRCm38.p3	8:88648102	GCTCCCAGTTTCTTG[A/G]CCACTTAATGCCAGT	257632
rs32621110	snp	A/G	0.5	0	missense	Nod2	GRCm38.p3	8:88663830	ACATCTTGGAGCTGC[A/G]GACTGAAGTGGGCAC	257632
rs32630558	snp	A/C	0.432133	0.171253	intron-variant	Nod2	Mm_Celera	8:88679702	TATGGTGTGTGACAC[A/C]ACTTCTCCTGGTGAG	257632
rs32631169	snp	G/T	0.5	0	intron-variant	Nod2	GRCm38.p3	8:88660402	TGTCAGCACTTAGAA[G/T]GGTTGGGATTTAAGA	257632
rs32636356	snp	C/G	0.444444	0.157135	intron-variant	Nod2	GRCm38.p3	8:88661049	CAGTGAGAGAGGCTC[C/G]GGTGACACGGCTAAA	257632
rs32639911	snp	A/G	0.444444	0.157135	intron-variant	Nod2	GRCm38.p3	8:88674521	ACATGATAGAAACAG[A/G]GGGGATTAAGAAGGA	257632
rs32653748	snp	A/G	0.5	0	intron-variant	Nod2	GRCm38.p3	8:88669138	GGTGAAATTAATGAT[A/G]CTACTGTTGGGGGGG	257632
rs32656069	snp	A/G	0.444444	0.157135	intron-variant	Nod2	GRCm38.p3	8:88661583	CCAATTAAGCAGGTG[A/G]ACATGGTTGTACACA	257632
rs32657909	snp	A/C	0.444444	0.157135	intron-variant	Nod2	Mm_Celera	8:88666811	ACAGACACCTTTGTG[A/C]AACTGTGTGTTGACT	257632
rs32664746	snp	C/T	0.465374	0.126941	intron-variant	Nod2	GRCm38.p3	8:88656475	AGAAGGCTAAGCAGG[C/T]GTATAGAAAATGTAA	257632
rs32674247	snp	A/G	0.473373	0.11227	intron-variant	Nod2	GRCm38.p3	8:88679426	CCTGGGATTCTTCCC[A/G]TAGACACTCCTAATT	257632
rs32682906	snp	C/T	0.475309	0.108333	intron-variant	Nod2	GRCm38.p3	8:88671086	GTGGTACCCAGGTGC[C/T]GGAATGTTCCCCAGA	257632
rs32690189	snp	A/T	0.5	0	intron-variant	Nod2	GRCm38.p3	8:88653650	GCTCTTCCCCAGCCA[A/T]AACCTCTACCCTTCA	257632
rs32694333	snp	A/T	0.444444	0.157135	intron-variant	Nod2	GRCm38.p3	8:88682177	AACCTGGCAGTTGCA[A/T]CCCTTTTGGGGGTTC	257632
rs32698083	snp	G/T	0.375	0.216506	intron-variant	Nod2	Mm_Celera	8:88667266	TTTGGCTAGGAAAAT[G/T]AATGAACATGATCTG	257632
rs32698902	snp	A/G	0.5	0	intron-variant	Nod2	GRCm38.p3	8:88661228	TACTTGGGAGAAGAA[A/G]CCACCAGTTGCAGAA	257632
rs32724915	snp	C/T	0.5	0	intron-variant	Nod2	GRCm38.p3	8:88686577	ACTTTCCTTGCAAGC[C/T]TTCACTCACACCTCC	257632
rs32745202	snp	C/T	0.444444	0.157135	intron-variant	Nod2	GRCm38.p3	8:88652715	TCATGGCAACTGCAG[C/T]TAGCTTTTGATATCC	257632
rs32753404	snp	A/G	0.444444	0.157135	intron-variant	Nod2	GRCm38.p3	8:88674856	CGGAGTGGCGCTATG[A/G]AAGCACATGAACACG	257632
rs32759574	snp	A/G	0.444444	0.157135	intron-variant	Nod2	GRCm38.p3	8:88666147	CCACAACCATGCTGG[A/G]CTCAGCAGGGCTCTT	257632
rs32773589	snp	C/T	0.444444	0.157135	intron-variant	Nod2	GRCm38.p3	8:88668957	TGAAAACCACTTCCC[C/T]GAGAGCCCTAGAAAA	257632
rs32791473	snp	A/G	0.444444	0.157135	intron-variant	Nod2	GRCm38.p3	8:88682247	AGCACAGATGTTTAC[A/G]TTAAGACTTATAACA	257632
rs32799724	snp	A/C	0.444444	0.157135	intron-variant	Nod2	GRCm38.p3	8:88682020	CTCGACACATATCCA[A/C]TCCAAGAGTGGAGCT	257632
rs32800817	snp	A/G	0.415225	0.187619	intron-variant	Nod2	Mm_Celera	8:88679082	TTATCCAATTAAATC[A/G]TCAAATCAGAGGCCA	257632
rs32807483	snp	C/T	0.444444	0.157135	intron-variant	Nod2	GRCm38.p3	8:88660951	GGATCTCTCAATCCA[C/T]GAAACGTAGTTTCTC	257632
rs32810926	snp	A/G	0.493827	0.0552116	intron-variant	Nod2	GRCm38.p3	8:88674386	GAGAGTGCTATGCAG[A/G]CCCAGTGCAGATGTC	257632
rs32848034	snp	A/G	0.49827	0.0293608	intron-variant	Nod2	GRCm38.p3	8:88652655	CTGTAGCAAGAGTAC[A/G]GGAGCCCAGGGACTC	257632
rs32848035	snp	A/G	0.5	0	intron-variant	Nod2	GRCm38.p3	8:88682603	TGTGTTCAGACATTG[A/G]TTGGAAAAATATTGG	257632
rs32854334	snp	C/T	0.5	0	intron-variant	Nod2	GRCm38.p3	8:88648010	GAAATGCCCCCTCCC[C/T]CATCTCTGCCCTCCT	257632
rs32855240	snp	C/T	0.465374	0.126941	intron-variant	Nod2	GRCm38.p3	8:88679268	GCTGCTTGCCAACCG[C/T]CTTGACTCTTGTATG	257632
rs32858426	snp	C/T	0.5	0	synonymous-codon	Nod2	GRCm38.p3	8:88664365	CCTCAGGAAGTTCGT[C/T]CGTACAGAGTGCCAA	257632
rs32861288	snp	C/T	0.486111	0.0821678	intron-variant	Nod2	GRCm38.p3	8:88674851	TGGGGCGGAGTGGCG[C/T]TATGGAAGCACATGA	257632
rs32868886	snp	C/T	0.444444	0.157135	intron-variant	Nod2	Mm_Celera	8:88666911	TAGCTCTGTTGCACA[C/T]AATAACTGTATAATA	257632
rs32903994	snp	C/G	0.444444	0.157135	intron-variant	Nod2	Mm_Celera	8:88653337	GTCTCAGAGGGTAAG[C/G]TGTGGCCTGTGTCAG	257632
rs32914338	snp	A/G	0.444444	0.157135	intron-variant	Nod2	GRCm38.p3	8:88661062	TCCGGTGACACGGCT[A/G]AAATGTACCAGGCAG	257632
rs32923110	snp	C/G	0.444444	0.157135	intron-variant	Nod2	GRCm38.p3	8:88661082	GTACCAGGCAGCCTG[C/G]CATACACTCTATGGA	257632
rs32926486	snp	A/G	0.375	0.216506	synonymous-codon	Nod2	Mm_Celera	8:88663780	TACTTACGATGGGTC[A/G]GAGAATCTTTGCCTG	257632
rs32929914	snp	C/T	0.46875	0.121031	intron-variant	Nod2	GRCm38.p3	8:88673328	AGAAACAAGGCCTTA[C/T]TGCCATGGAGCTCTC	257632
rs32933916	snp	C/T	0.375	0.216506	intron-variant	Nod2	GRCm38.p3	8:88673846	ACAATGCCTTATCTA[C/T]AGAGCAGTGTTCCCA	257632
rs32934188	snp	A/T	0.444444	0.157135	intron-variant	Nod2	GRCm38.p3	8:88666874	TAACATAATATGGTG[A/T]GTTGTATATGCAGTT	257632
rs33005423	snp	A/G	0.5	0	intron-variant	Nod2	GRCm38.p3	8:88674041	AATACCATGGTGGCA[A/G]GAGGTTGTGGGAGAG	257632
rs33025491	snp	A/G	0.426035	0.177515	intron-variant	Nod2	GRCm38.p3	8:88652303	TACAGAGGCAGGGCT[A/G]CGGGGATAACCAAAG	257632
rs33029774	snp	A/C	0.5	0	intron-variant	Nod2	GRCm38.p3	8:88652250	TTGGCATCTTTACAG[A/C]AATCCCCAGATCTAT	257632
rs33110890	snp	A/G	0.444444	0.157135	intron-variant	Nod2	GRCm38.p3	8:88673387	GGACATTTATGTACC[A/G]CCTAGCTTTTATGGT	257632
rs33112860	snp	A/G	0.277778	0.248452	intron-variant	Nod2	Mm_Celera	8:88674373	TTTCAGAGTGCGTGA[A/G]AGTGCTATGCAGACC	257632
rs33148979	snp	C/G	0.375	0.216506	intron-variant	Nod2	Mm_Celera	8:88675150	AACTTGAGGGTTTGG[C/G]GGTGAATTTGGAGGT	257632
rs33149135	snp	C/G	0.444444	0.157135	intron-variant	Nod2	GRCm38.p3	8:88655585	TGATGCCAGCTGTCC[C/G]TGTGACTCATGCAGA	257632
rs33152263	snp	A/G	0.432133	0.171253	intron-variant	Nod2	GRCm38.p3	8:88674992	TAAAGTGGCTCAGGT[A/G]AGTTGCAAGATGTGT	257632
rs33173211	snp	C/T	0.432133	0.171253	intron-variant	Nod2	GRCm38.p3	8:88680202	TTGTTTACCTTCTTG[C/T]TTAAGGAGTCTCCCT	257632
rs33177612	snp	C/T	0.5	0	intron-variant	Nod2	GRCm38.p3	8:88679424	ATCCTGGGATTCTTC[C/T]CGTAGACACTCCTAA	257632
rs33204454	snp	A/G	0.475309	0.108333	intron-variant	Nod2	GRCm38.p3	8:88652609	GGAGGGAACTGACCC[A/G]CAGAAGCTGGCTTCT	257632
rs33208275	snp	C/T	0.5	0	synonymous-codon	Nod2	GRCm38.p3	8:88664368	CAGGAAGTTCGTCCG[C/T]ACAGAGTGCCAACTG	257632
rs33209427	snp	A/G	0.444444	0.157135	intron-variant	Nod2	GRCm38.p3	8:88673415	GGTTTTTCGAGACAG[A/G]GTTTCTCTGTGTAGT	257632
rs33210632	snp	C/T	0.396694	0.202437	intron-variant	Nod2	GRCm38.p3	8:88680051	GGCAACTGGTCTGGT[C/T]TCAGAACCTTCTTTG	257632
rs33218695	snp	A/G	0.444444	0.157135	intron-variant	Nod2	GRCm38.p3	8:88682668	TACCACAATTCTTAG[A/G]TCAGGTGGCTAGGAC	257632
rs33219591	snp	C/G	0.5	0	intron-variant	Nod2	GRCm38.p3	8:88680609	TAGGAACTAGGAGGG[C/G]TTTAGGTAGCTCCAC	257632
rs33236045	snp	A/G	0.432133	0.171253	intron-variant	Nod2	GRCm38.p3	8:88673951	ATAAGCAGCTTTAGG[A/G]AAGATATGTTTATTT	257632
rs33296163	snp	A/G	0.5	0	downstream-variant-500B	Nod2	GRCm38.p3	8:88688728	CTCCTGGTGGCTGTC[A/G]AAGTGAGTAGATGTC	257632
rs33306176	snp	A/T	0.444444	0.157135	intron-variant	Nod2	Mm_Celera	8:88666941	AGAAATATGAATAGC[A/T]CCATCAGGGTCTTGA	257632
rs33307887	snp	C/T	0.375	0.216506	intron-variant	Nod2	GRCm38.p3	8:88667062	GGGAAAAGCCTGAAG[C/T]GAGAGAGGATTTGCT	257632
rs33318219	snp	C/T	0.197531	0.244432	intron-variant	Nod2	Mm_Celera	8:88679719	CTTCTCCTGGTGAGA[C/T]GTAATGTACAAGTCT	257632
rs33321591	snp	A/G	0.5	0	synonymous-codon	Nod2	GRCm38.p3	8:88660616	GCACGTCAGGGAACT[A/G]CCAGCTCCACTGCCT	257632
rs33338846	snp	C/T	0.444444	0.157135	intron-variant	Nod2	GRCm38.p3	8:88674309	GGGCAGGCTGTATTT[C/T]TTAAGTATTTCTTGG	257632
rs33344760	snp	C/T	0.375	0.216506	intron-variant	Nod2	GRCm38.p3	8:88667524	ATGCGCCACCACGCC[C/T]GGCAGGGCCACTCCT	257632
rs33403077	snp	A/C	0.444444	0.157135	intron-variant	Nod2	GRCm38.p3	8:88681920	CAGAAAGGGCTGGCG[A/C]CTGTGGAAGGTGGAT	257632
rs33425875	snp	C/T	0.48	0.0979796	intron-variant	Nod2	GRCm38.p3	8:88655656	ACTTGCTTGCTTCTG[C/T]CATAGAACCACTAAG	257632
rs33427249	snp	A/G	0.345679	0.230967	intron-variant	Nod2	GRCm38.p3	8:88681995	AGCCTTCGGGAGTTG[A/G]CAGAACAAGCTCGAC	257632
rs33437194	snp	A/G	0.375	0.216506	intron-variant	Nod2	GRCm38.p3	8:88660807	AAAAGATGAGGGCAT[A/G]GCGGCTCTCCCCCTT	257632
rs33450100	snp	C/T	0.495868	0.0452663	intron-variant	Nod2	Mm_Celera	8:88668992	TCGGGGAGGCTGCAC[C/T]GTGCTGTGCTTAAGC	257632
rs33471863	snp	A/G	0.5	0	intron-variant	Nod2	GRCm38.p3	8:88669133	CTTGGGGTGAAATTA[A/G]TGATACTACTGTTGG	257632
rs33480353	snp	C/T	0.444444	0.157135	intron-variant	Nod2	GRCm38.p3	8:88655209	TTGACCTTTTAATTT[C/T]TTTATAGAGGTGGCT	257632
rs33494486	snp	A/C	0.432133	0.171253	intron-variant	Nod2	GRCm38.p3	8:88682597	TATGTGTGTGTTCAG[A/C]CATTGATTGGAAAAA	257632
rs33498355	snp	C/T	0.444444	0.157135	intron-variant	Nod2	Mm_Celera	8:88661770	CCAAATTTCATTTTG[C/T]CTACTTATTTTTTTT	257632
rs33500855	snp	A/G	0.401235	0.199068	intron-variant	Nod2	GRCm38.p3	8:88679174	TCTCTGATTTACACA[A/G]CCAAGCTCCTGATTG	257632
rs33503962	snp	C/G	0.396694	0.202437	intron-variant	Nod2	GRCm38.p3	8:88673392	TTTATGTACCACCTA[C/G]CTTTTATGGTTTTTC	257632
rs33573501	snp	C/G	0.497041	0.0383476	intron-variant	Nod2	Mm_Celera	8:88669007	TGTGCTGTGCTTAAG[C/G]GCAGGTTGGCAGCCC	257632
rs33576011	snp	G/T	0.465374	0.126941	intron-variant	Nod2	GRCm38.p3	8:88675381	ACTCGCCCTTCATAG[G/T]TCAGTTGACCAGTCT	257632

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