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
rs908225	snp	C/T	0.469346	0.119947	intron-variant	TOLLIP	GRCh38.p7	11:1291999	TCCTTTCACTTCTAA[C/T]CAAAGCTGTGGCCGG	54472
rs2271599	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	TOLLIP, LOC105376512	GRCh38.p7	11:1298116	TTGCAGAAACAGACT[C/T]GTGCTAACCAAGTTC	54472
rs2292635	snp	C/T	0.0973687	0.197999	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289915	GTGCACGCTCTGTCC[C/T]TGGAAATCCCACCTG	54472
rs3168046	snp	C/T	0.481627	0.0940692	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275419	AATGAAGGTGTCAGG[C/T]GGGACTGGAACGTTC	54472
rs3750920	snp	C/T	0.480178	0.0975602	synonymous-codon, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288726	CTGCCTCAGGGACTC[C/T]GGGATGGTGATGTGG	54472
rs3793962	snp	C/G	0.174288	0.23826	intron-variant	TOLLIP	GRCh38.p7	11:1278274	CTCCTCCTGCAGCAG[C/G]AGCTGCAGCAGTGCA	54472
rs3793963	snp	C/T	0.176861	0.239062	intron-variant	TOLLIP	GRCh38.p7	11:1280678	TGGGGAGGCGCCGGA[C/T]GCCCCACTTTCCAGG	54472
rs3793964	snp	C/T	0.469839	0.119042	intron-variant	TOLLIP	GRCh38.p7	11:1280752	CAGGAGGAGGGAAAG[C/T]GAGGAGGGCCCCAGA	54472
rs3793965	snp	C/T	0.481319	0.0948228	intron-variant	TOLLIP	GRCh38.p7	11:1281477	TGGGCTCAGACACCA[C/T]GGGAGGCTCTCGGGG	54472
rs3793966	snp	C/T	0.495855	0.045338	intron-variant	TOLLIP	GRCh38.p7	11:1281718	ACAGGCCCGAAGCCA[C/T]GCAGCCAGCACCGCG	54472
rs3793967	snp	C/G	0	0	intron-variant	TOLLIP	GRCh38.p7	11:1285002	CTGGGGTGCTGACCA[C/G]GCCTCTCCACTCCAG	54472
rs3793968	snp	C/T	0.126219	0.217206	intron-variant	TOLLIP	GRCh38.p7	11:1294063	TTTCTATGAAAGCCG[C/T]GTGGCTCACAGTGTG	54472
rs3793969	snp	A/T	0.487995	0.0765403	intron-variant, downstream-variant-500B	TOLLIP, LOC105376512	GRCh38.p7	11:1297654	CCGTACTGCGAGAAC[A/T]AGCAGAGCACCCCGG	54472
rs3793970	snp	C/T	0.485118	0.0849685	intron-variant, downstream-variant-500B	TOLLIP, LOC105376512	GRCh38.p7	11:1297667	ACAAGCAGAGCACCC[C/T]GGCTTCACCTCCGGA	54472
rs3817288	snp	A/C/G/T	0.00557542	0.0525036	intron-variant	TOLLIP	GRCh38.p7	11:1285909	GGGGCTTAGAGCGCC[A/C/G/T]GGGTGGGGACGTCAT	54472
rs3829223	snp	C/T	0.495999	0.0445491	intron-variant	TOLLIP	GRCh38.p7	11:1279176	AACCTGCTCTGCTGA[C/T]AATGAGGGGATGTGG	54472
rs3838783	in-del	-/G	0.47767	0.103278	intron-variant	TOLLIP	GRCh38.p7	11:1283477	CGCATGCCTGGGCAT[-/G]GGGGCTGGGGGCTCC	54472
rs4963034	snp	C/T	0.00517822	0.0506191	intron-variant	TOLLIP	GRCh38.p7	11:1293207	AGCCACCTGCGGACA[C/T]GGGGGAGAAGCCGGG	54472
rs4963060	snp	A/G	0.299411	0.245069	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299830	CCGTCAAAACGCCCC[A/G]TCCACCAGCCAGGCA	54472
rs4963061	snp	A/G	0.333722	0.235565	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303350	CCAGAGAGGGACGGC[A/G]TGTGACGTGGCAGGC	54472
rs4963062	snp	A/G	0.332568	0.235971	intron-variant	TOLLIP	GRCh38.p7	11:1305411	CCACGGGCTCTTCAC[A/G]ACACTCAGGGGAGAG	54472
rs5743851	snp	C/T	0.0588605	0.161139	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310590	GTACGCTTGTTTATA[C/T]GTAAGATAAAAGCCA	54472
rs5743852	snp	C/T	0.0228947	0.104514	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310141	GGGCTCTTCTGGCAG[C/T]GCCTCCATCCCCGTT	54472
rs5743853	snp	A/G	0.0215028	0.101435	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310128	AGNGCCTCCATCCCC[A/G]TTCCGTTCACCCGGC	54472
rs5743854	snp	C/G	0.385741	0.209939	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310024	TGAGGGAAAGATCGC[C/G]CTGCAGGGGATGTCG	54472
rs5743855	in-del	-/T/TCCCG/TCCCGGCACCCTTATGGCCCCACAGGTGGAGGC/TCCCGGCACCCTTATGGCCCCACAGGTGGAGGCGG	0.143457	0.22616	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308834	CCCAGGTGGAGGCGG[lengthTooLong]GGGCCTGCACTCTAG	54472
rs5743856	snp	A/G	0.093417	0.194889	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308608	CTGGCAGTTTCTTCT[A/G]TAGCATTAATATTGC	54472
rs5743857	snp	C/T	0.0984431	0.198823	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308340	TTACACGTCACATGG[C/T]GAAAGCAGCAAGAGA	54472
rs5743858	snp	A/G	0.0130921	0.0798413	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308097	CAGGCTGTCGTGAGC[A/G]GTACAGTTTTTATCA	54472
rs5743859	snp	C/T	0.144296	0.226554	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308045	TGGGTGGAAAAAGTC[C/T]TTTTTCACGATGCTC	54472
rs5743860	snp	C/G	0.0252325	0.109451	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308012	AGGTCCCTGCCCTCG[C/G]GCAGCCCAGTACTGG	54472
rs5743861	snp	A/G	0.0228947	0.104514	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1307953	CACCCTTAACACTGT[A/G]TCCACAAGTCCTGGT	54472
rs5743862	snp	C/T	0.0228947	0.104514	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1307792	TGTGGAGCCTACGGG[C/T]CGGCAGAGGTCCTGG	54472
rs5743863	snp	C/T	0.0588605	0.161139	intron-variant	TOLLIP	GRCh38.p7	11:1307682	AGTGCTCCTTTCTGC[C/T]TAACAGGAGACTCAG	54472
rs5743864	snp	C/T	0.332337	0.236052	intron-variant	TOLLIP	GRCh38.p7	11:1307641	GAACCAGCACCCTGC[C/T]GTTGTGTCCTCCTGG	54472
rs5743865	snp	C/T	0.00159617	0.0282053	intron-variant	TOLLIP	GRCh38.p7	11:1307373	GGAGATGTTCTCACA[C/T]GCAGGGCCTGTGCTG	54472
rs5743866	snp	A/C/G	0.00597534	0.0543715	intron-variant	TOLLIP	GRCh38.p7	11:1307266	TATTTCAGGGGCACC[A/C/G]CCGTTGACCGGTAAA	54472
rs5743867	snp	C/T	0.333722	0.235565	intron-variant	TOLLIP	GRCh38.p7	11:1307121	ACCAACTGTGGCGTT[C/T]AGGATGGCCATGATG	54472
rs5743868	snp	A/G	0.0228947	0.104514	intron-variant	TOLLIP	GRCh38.p7	11:1306926	TGTTGGGGTGAGGAC[A/G]TGACATCTCTCGGAG	54472
rs5743869	snp	G/T	0.0865458	0.189163	intron-variant	TOLLIP	GRCh38.p7	11:1306522	ACACCTGTGGTGCCA[G/T]AGAGGCAGGAGGTTA	54472
rs5743870	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1306346	AAGGAGCAGAGGGGC[C/T]GCTAATGGGGTCCTG	54472
rs5743871	snp	A/G	0.0228947	0.104514	intron-variant	TOLLIP	GRCh38.p7	11:1306129	CGTTTCAAAAAGGCC[A/G]GTATTTTGGAAAGAT	54472
rs5743872	snp	C/G/T	0.0494526	0.149365	intron-variant	TOLLIP	GRCh38.p7	11:1306002	CCCTGCGAGGGGTAC[C/G/T]GTGTGGACCCCTGTG	54472
rs5743873	snp	A/G	0.00953873	0.0683987	intron-variant	TOLLIP	GRCh38.p7	11:1305980	ACCCCTGTGAGGAGT[A/G]TCATGGGGGCCCCTG	54472
rs5743874	snp	C/T	0.0930568	0.194599	intron-variant	TOLLIP	GRCh38.p7	11:1305954	CCCTGCGAGGGGTAC[C/T]GTGCGGGCCCCCGCG	54472
rs5743875	snp	A/G/T	0.0215028	0.101435	intron-variant	TOLLIP	GRCh38.p7	11:1305939	CGTGCGGGCCCCCGC[A/G/T]AGGAGTATCGAGGAG	54472
rs5743876	snp	A/G	0.0126979	0.078662	intron-variant	TOLLIP	GRCh38.p7	11:1305919	GTATCGAGGAGTACC[A/G]TGTGGACCCCTGCCT	54472
rs5743877	snp	A/G	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1305735	AGTCCAGCTGGAGGC[A/G]GCCTGGCCCCTCCCT	54472
rs5743878	snp	C/G	0.00279162	0.0372561	intron-variant	TOLLIP	GRCh38.p7	11:1305698	CTGAGAGGCCTGTTC[C/G]TGTCCAGGTCCCCTC	54472
rs5743879	snp	A/G	0.0912534	0.193131	intron-variant	TOLLIP	GRCh38.p7	11:1305596	CTTTATCACTTCTTC[A/G]GTGTTTATTAACTGG	54472
rs5743880	snp	C/T	0.00557542	0.0525036	intron-variant	TOLLIP	GRCh38.p7	11:1305547	GCTTTCCCCATCAAC[C/T]GGTGTCGGCTGGCTG	54472
rs5743881	snp	C/T	0.131723	0.220251	intron-variant	TOLLIP	GRCh38.p7	11:1305516	TCCTGAAACACAATT[C/T]GTGAAAGAAAGGCAA	54472
rs5743882	snp	C/T	0.00438332	0.0466095	intron-variant	TOLLIP	GRCh38.p7	11:1305475	TTTCCCTCATCTTCC[C/T]GTACCTCAAGGAGAG	54472
rs5743883	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1305317	CTGCTCCTGGGAGGG[C/T]GTCCGTTCCTGCNGA	54472
rs5743884	snp	C/T	0.0252325	0.109451	intron-variant	TOLLIP	GRCh38.p7	11:1305304	GGCGTCCGTTCCTGC[C/T]GACTGCACCTGAGCC	54472
rs5743885	snp	C/T	0.334412	0.235318	intron-variant	TOLLIP	GRCh38.p7	11:1305068	TACTGGCATGGCCAC[C/T]CCAGCTGTCTTTTAG	54472
rs5743886	snp	A/G	0.0228947	0.104514	intron-variant	TOLLIP	GRCh38.p7	11:1304984	TTTTGTTTAAGACAC[A/G]TGCACCATCGATAGC	54472
rs5743887	snp	A/G	0.00279162	0.0372561	intron-variant	TOLLIP	GRCh38.p7	11:1304909	TTTTGATGGGAATGC[A/G]CTAGTTTCATCTTTC	54472
rs5743888	snp	A/G	0.0252325	0.109451	intron-variant	TOLLIP	GRCh38.p7	11:1304815	TTTTATTTGTCCTAC[A/G]TTTTCTTATTTTTTT	54472
rs5743889	snp	G/T	0.0228947	0.104514	intron-variant	TOLLIP	GRCh38.p7	11:1304802	ACNTTTTCTTATTTT[G/T]TTTCTCTCATTGCCT	54472
rs5743890	snp	A/G	0.0912534	0.193131	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1304599	AATAAATAAAGAAGA[A/G]GTTAATCATTGTCTG	54472
rs5743891	snp	A/G	0.101301	0.200969	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1304158	GCTGCTGAGCAGCCC[A/G]GGAGTGGATGTCCCT	54472
rs5743892	snp	A/C	0.0955749	0.196603	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1304103	GCCCTCTGTTTGCTG[A/C]CTTCTGAATACGCTG	54472
rs5743893	snp	A/G	0.00557542	0.0525036	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303810	ggtctcaagtgatcc[A/G]cccacctcagcctcc	54472
rs5743894	snp	A/G	0.138207	0.223612	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303542	GCCCTGTTTCTTTGC[A/G]CAGCGCCTCCTGCCG	54472
rs5743895	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303292	TGACTGGCTTTTGTT[C/T]CATCTGAATGAGAAG	54472
rs5743896	snp	C/G	0.0588605	0.161139	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303195	TTCCTGGCAGAGACC[C/G]CATTTAAAGTCGCTT	54472
rs5743897	snp	A/C	0.127599	0.217986	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1302839	GGGCTGCTGAGCGGC[A/C]GTGGGAGGAGGATGT	54472
rs5743898	snp	C/T	0.0952156	0.196321	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1302514	CAGCAGCTGAGTGGG[C/T]ATGGGGAATTGCAGT	54472
rs5743899	snp	A/G	0.44858	0.151875	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1302334	TCTCTGAAACCCTGC[A/G]CACTGAGGGGTCAGT	54472
rs5743900	snp	C/G	0.127944	0.218179	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1302054	CAAGGCAGGGCCAGC[C/G]CCTCAGACACAGCAG	54472
rs5743901	snp	C/T	0.332568	0.235971	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301982	CTGGACCAACTGTGC[C/T]GTTCTATGTGAGTCC	54472
rs5743902	snp	A/G	0.484561	0.0864924	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301981	TGGACCAACTGTGCT[A/G]TTCTATGTGAGTCCT	54472
rs5743903	snp	C/T	0.0352966	0.128072	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301806	CCTTTAGCCACGAGC[C/T]CAGCCCAGGTCTTCC	54472
rs5743904	snp	A/G	0.334871	0.235153	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301568	GAGGAAACTTCTGGG[A/G]TTTGGCGGCCGTGTG	54472
rs5743905	snp	C/G	0.0912534	0.193131	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301483	GGGTTTTCTGGGTGT[C/G]CCAGCACATGGATAC	54472
rs5743906	snp	A/G	0.00597247	0.0543191	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301458	GGATACGGAGTTCTC[A/G]GAAGCCCGCGACACA	54472
rs5743907	snp	C/T	0.334871	0.235153	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301391	GGGTGGGCAGGCGCC[C/T]GCGGATGCCGTTTGT	54472
rs5743908	snp	C/G	0.00279162	0.0372561	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301355	atcctcagtgctggt[C/G]tgagactctggcttg	54472
rs5743909	snp	A/C	0.333491	0.235646	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300805	GGCCAGCCGTGCTTC[A/C]GGGGCGACTGTGGTG	54472
rs5743910	snp	A/C	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300763	GGTGATGTCTCCTGG[A/C]AGGCGTGAGGCCAGG	54472
rs5743911	snp	A/G	0.495745	0.0459295	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300719	AGGACTCCACGTCCT[A/G]GGCTGAGCTGGGCTC	54472
rs5743912	snp	A/G	0.0681886	0.171594	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300639	CTCTCAGTCGGAAAC[A/G]TATTCCTAACAGGTG	54472
rs5743913	snp	A/C	0.0490535	0.14873	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300456	ATTAAGACTTTATTT[A/C]TGTGCCAAAACTAAA	54472
rs5743914	snp	A/G	0.00358779	0.0422022	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300379	GACCTCTTTTCTTTC[A/G]TGTGGAAAGGTANGC	54472
rs5743915	snp	C/T	0.489083	0.0730708	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300366	TCGTGTGGAAAGGTA[C/T]GCTGCAGTGGTTTAG	54472
rs5743916	snp	G/T	0.0228947	0.104514	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300145	CTCTGTGGGATGAGA[G/T]CCCTACCCTGTCCTT	54472
rs5743917	snp	C/T	0.0861826	0.188849	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300109	TTTAAAAGTAATTCA[C/T]GAATGTTTTTAAAAA	54472
rs5743918	snp	A/G	0.0785177	0.181917	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300108	TTAAAAGTAATTCAC[A/G]AATGTTTTTAAAAAG	54472
rs5743919	snp	A/G	0.107694	0.205546	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299900	AGTCTCCATGTGTTC[A/G]CGGCAGGGACCGCCG	54472
rs5743920	snp	C/T	0.127599	0.217986	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299868	CTCCTGGTGAGGCCG[C/T]GTGGCGATGCGCTGG	54472
rs5743921	snp	A/G	0.0345262	0.126772	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299719	TGTTGGCCTTCACAC[A/G]GGCATTTAGACTTGT	54472
rs5743922	snp	A/G	0.0588605	0.161139	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299442	TCACTGAAACGATAG[A/G]GTTTACTTCAGCACC	54472
rs5743923	snp	C/G	0.127599	0.217986	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299264	CAGTATTTGTACGGG[C/G]AGGACTGAAGCCTGG	54472
rs5743924	snp	A/G	0.0912534	0.193131	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299043	GCTGGGGGCATGACT[A/G]TTGGCTCCAGGTTTT	54472
rs5743925	snp	A/C	0.00119737	0.0244387	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298599	AAATGACACTTGATC[A/C]TTAGGCCTTTGGATA	54472
rs5743926	snp	A/G	0.021333	0.101051	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298511	AGTGCAGAGCAAGGA[A/G]ATGGAGCGCTGGACG	54472
rs5743927	snp	C/G	0.0228947	0.104514	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298286	CTGTCTGTCCCCTAC[C/G]TGTGCCCAGGAGGGC	54472
rs5743928	snp	A/G	0.00597247	0.0543191	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298263	AGGAGGGCACGAGCC[A/G]CCTGTCTGTCTGCCA	54472
rs5743929	snp	C/G	0.00953873	0.0683987	intron-variant, downstream-variant-500B	TOLLIP, LOC105376512	GRCh38.p7	11:1298128	TGTTAGTCCTGAGAA[C/G]TTGGTTAGCACGAGT	54472

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