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
rs914715	snp	A/T	0.0391387	0.134304	intron-variant	TLE4	GRCh38.p7	9:79695983	AGAAATCAACACCCA[A/T]TAAGACAAACATCTC	7091
rs946806	snp	C/T	0.498206	0.0298983	upstream-variant-2KB	TLE4	GRCh38.p7	9:79570457	GAAATGGGGGCGGCC[C/T]CCGTCAGTGCGCCTT	7091
rs1051250	snp	C/T	0	0	missense, nc-transcript-variant	TLE4	GRCh38.p7	9:79708721	GGGCTCCACAACATC[C/T]CCCCTCAGATGAGCG	7091
rs1113107	snp	C/T	0.388587	0.208071	intron-variant	TLE4	GRCh38.p7	9:79602539	AATGGAACTACAAAG[C/T]CTGGGTGACAGCACA	7091
rs1132275	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TLE4	GRCh38.p7	9:79725575	AGGtttaaaataatt[A/G]atttaaaatGTCACT	7091
rs1132276	snp	A/G	0	0	utr-variant-3-prime, nc-transcript-variant	TLE4	GRCh38.p7	9:79725595	AAAATGTCACTAAGT[A/G]TAGACTGATGACTGT	7091
rs1316822	snp	C/T	0.210301	0.246828	intron-variant	TLE4	GRCh38.p7	9:79686991	GTGTCTGCACCTGAC[C/T]AGATGATACCAAATG	7091
rs1316823	snp	C/T	0.494774	0.0508504	intron-variant	TLE4	GRCh38.p7	9:79686880	CAAGTACTTCACTGA[C/T]GATGAAACACAACTG	7091
rs1417081	snp	C/G	0.361474	0.223771	intron-variant	TLE4	GRCh38.p7	9:79605230	TAATTTTCTTTCTCT[C/G]CTCCTTCTGACATCC	7091
rs1475674	snp	C/G	0.456968	0.140229	intron-variant	TLE4	GRCh38.p7	9:79671371	CTACCCTGACGAGCT[C/G]AACGAGTGGCCCGAG	7091
rs1475675	snp	C/T	0.181022	0.240296	intron-variant	TLE4	GRCh38.p7	9:79674086	AGAGTTGAGAAGTGG[C/T]TTATTGCTTTTCTCA	7091
rs1475676	snp	G/T	0.494936	0.050064	intron-variant	TLE4	GRCh38.p7	9:79674238	ATAATAATTAGCACT[G/T]TGGGTGCATATACTC	7091
rs1547275	snp	C/T	0.166506	0.235645	intron-variant	TLE4	GRCh38.p7	9:79703554	CAGAGAATGACTCTA[C/T]CTGCCATGAAGGTCA	7091
rs1547276	snp	A/C	0.186421	0.24178	intron-variant	TLE4	GRCh38.p7	9:79702669	ATACTCTAGCCCTAG[A/C]CCTATCAAACGTTCA	7091
rs1930256	snp	C/T	0.0832709	0.186283	intron-variant	TLE4	GRCh38.p7	9:79644574	ATTTGGGAAGCATCA[C/T]AATGAAGTGGCCTCA	7091
rs1930257	snp	A/C	0.413416	0.189196	intron-variant	TLE4	GRCh38.p7	9:79714325	CTTCCCTTTTATAGC[A/C]TTACATTGATTTTAA	7091
rs1930258	snp	C/T	0.00636936	0.0560724	intron-variant	TLE4	GRCh38.p7	9:79700768	GAAAGCAAAATACCC[C/T]GAATGTGAATGTTTA	7091
rs1930259	snp	C/T	0.368733	0.220005	intron-variant	TLE4	GRCh38.p7	9:79699494	GGTAATTGCAAGTCC[C/T]GGTTTGCCCTTTCTA	7091
rs1934610	snp	C/T	0.0386831	0.13359	synonymous-codon, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	TLE4	GRCh38.p7	9:79572835	GCCGCCCGCACTCAC[C/T]GGGTGTCTGGTCTGC	7091
rs2016420	snp	G/T	0.224709	0.248717	intron-variant	TLE4	GRCh38.p7	9:79713896	TGAGAGAGAGTCTCG[G/T]TCTGTCACCCACGCT	7091
rs2027005	snp	G/T	0.489893	0.0703642	intron-variant	TLE4	GRCh38.p7	9:79660676	TAATTTGTTCAGTAT[G/T]AATTGATACCTGCCT	7091
rs2027006	snp	A/G	0.0422008	0.138995	intron-variant	TLE4	GRCh38.p7	9:79653660	TTCAGCATCCTTACT[A/G]TGAATTATAATATTA	7091
rs2095097	snp	C/T	0.0228947	0.104514	intron-variant	TLE4	GRCh38.p7	9:79661247	TTTGTATTCTTACAG[C/T]AACACTAACCCCACT	7091
rs2151147	snp	C/T	0.0283406	0.115616	intron-variant	TLE4	GRCh38.p7	9:79686877	GTACTTCACTGATGA[C/T]GAAACACAACTGACA	7091
rs2211188	snp	A/G			intron-variant	TLE4	GRCh38.p7	9:79599842	agagccctggggcag[A/G]aggtgggtctgattt	7091
rs2297498	snp	A/G	0.496314	0.0427728	intron-variant	TLE4	GRCh38.p7	9:79671437	GCCTCTTTTATTTTC[A/G]TGTCAGATTATCTGT	7091
rs2297499	snp	C/G	0.471421	0.116626	intron-variant	TLE4	GRCh38.p7	9:79652817	ACTCTCTTGGAATGC[C/G]AATCTGAGATGACCT	7091
rs2378422	snp	C/T			intron-variant	TLE4	GRCh38.p7	9:79592216	TTCTTCTTCTTCTTC[C/T]TCTTCTTCTTCTTCT	7091
rs2791566	snp	C/T	0	0	intron-variant	TLE4	GRCh38.p7	9:79574999	CCAAAAACAAGAATA[C/T]GTTTAAATTGCTGGG	7091
rs2791567	snp	C/T	0.378372	0.214524	intron-variant	TLE4	GRCh38.p7	9:79577443	TTATGTCAATATTAG[C/T]ATTATAGTATAGTTT	7091
rs2791568	snp	A/G	0.0429648	0.14013	intron-variant	TLE4	GRCh38.p7	9:79581059	TTTAAGATTATTTAC[A/G]CGCTGATAATATTCC	7091
rs2791569	snp	A/C	0.494057	0.0541878	intron-variant	TLE4	GRCh38.p7	9:79585202	TTTTAGATTGCTTAT[A/C]GTGTCGATAATATTT	7091
rs2791570	snp	C/T	0.493969	0.05458	intron-variant	TLE4	GRCh38.p7	9:79586186	GACTGTCCTGGCCAA[C/T]GTGGTGAAACGCTGT	7091
rs2791571	snp	C/T	0.190205	0.242744	intron-variant	TLE4	GRCh38.p7	9:79586196	GCCAATGTGGTGAAA[C/T]GCTGTCTCTACTAAA	7091
rs2791572	snp	C/G	0.419936	0.183362	intron-variant	TLE4	GRCh38.p7	9:79589032	AGTTGCTACTGGCAT[C/G]TAGTGGGTAGAGTCT	7091
rs2791573	snp	A/G	0.416545	0.186448	intron-variant	TLE4	GRCh38.p7	9:79591715	TTGACATTTCATTGG[A/G]TGAGGAGTATGGAAA	7091
rs2791574	snp	G/T	0.482609	0.0916147	intron-variant	TLE4	GRCh38.p7	9:79597179	GCCTCCTTTCCTTGC[G/T]CTCACCACGGTCACC	7091
rs2791575	snp	C/T	0.00119737	0.0244387	intron-variant	TLE4	GRCh38.p7	9:79618857	ATGAAATAAAGAAGA[C/T]GTTATTCTTTTTACA	7091
rs2791576	snp	A/G	0.430285	0.173197	intron-variant	TLE4	GRCh38.p7	9:79619967	TGTATTTTGGTGACA[A/G]TTGGCTGCTTGGTGA	7091
rs2791577	snp	A/T	0.499977	0.00339449	intron-variant	TLE4	GRCh38.p7	9:79621279	GCCATACCTGGAGTA[A/T]TGTGCACTACAAGGA	7091
rs2807301	snp	A/G	0.493969	0.05458	intron-variant	TLE4	GRCh38.p7	9:79585338	TCAAACCCAAGATCT[A/G]TTTTACCGGCTAGCT	7091
rs2807302	snp	C/T	0.404907	0.196224	intron-variant	TLE4	GRCh38.p7	9:79582820	TATAGGACCACTGAA[C/T]CTACCACCATTGCTG	7091
rs2807303	snp	C/T	0.491834	0.0633738	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	TLE4	GRCh38.p7	9:79572180	CTCATTTCCTTATTT[C/T]TCTTCCTTCCTGTTT	7091
rs2807304	snp	C/T	0.404733	0.196361	upstream-variant-2KB	TLE4	GRCh38.p7	9:79570439	GTCAGTGCGCCTTTC[C/T]ATCCTTAGTCCGTGT	7091
rs2807307	snp	A/C	0.418169	0.184985	intron-variant	TLE4	GRCh38.p7	9:79618591	CCTTGGCACCCAGTG[A/C]CTAGAAACAAGTCTG	7091
rs2807308	snp	A/C	0.410568	0.191619	intron-variant	TLE4	GRCh38.p7	9:79614782	AAGAAAAATCTCATA[A/C]TGTTTTAAGAAAGTT	7091
rs2807309	snp	A/C	0.213635	0.247341	intron-variant	TLE4	GRCh38.p7	9:79610322	TGGCCTATGTTTTGA[A/C]ACTGAGTCTAATATA	7091
rs2807310	snp	C/T	0.380333	0.213338	intron-variant	TLE4	GRCh38.p7	9:79610138	CTGCTCACTGAACTG[C/T]GACCTGCTTTCTGAT	7091
rs2807312	snp	A/G	0.162253	0.234095	intron-variant	TLE4	GRCh38.p7	9:79600997	AGAAGCACCCTAGGA[A/G]AGCACCTTGTATACA	7091
rs3057745	in-del	-/CTC			intron-variant	TLE4	GRCh38.p7	9:79592212	ttcttcttcttcttc[-/CTC]ttcctcttcttcttc	7091
rs3186577	snp	C/T	1.65861e-05	0.00287972	synonymous-codon, nc-transcript-variant	TLE4	GRCh38.p7	9:79652637	TGGACATGGTCTCCC[C/T]GTACCTCTGACTCCA	7091
rs3216009	in-del	-/GGGTCA			intron-variant	TLE4	GRCh38.p7	9:79573590	GTTAGCGGGGGGTGA[-/GGGTCA]TCGCGCACGCAAGCA	7091
rs3739884	snp	A/G	0.00119737	0.0244387	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	TLE4	GRCh38.p7	9:79571805	TTGACTACAATCACC[A/G]GCCCGCCATGCGAGC	7091
rs3802500	snp	A/G	0.00119737	0.0244387	intron-variant	TLE4	GRCh38.p7	9:79706996	TCACATTTTTAACAG[A/G]ACTTTTATTTCCAAA	7091
rs3818877	snp	C/T	0.00835141	0.0640778	intron-variant	TLE4	GRCh38.p7	9:79612958	AGCAAAATATTTTAA[C/T]GACTGAATTTTGCTT	7091
rs3839905	snp	G/T			utr-variant-3-prime, nc-transcript-variant	TLE4	GRCh38.p7	9:79725678	TTATTAGGTTTTTTT[G/T]GTTTTTGTTTTCTAC	7091
rs3898860	snp	A/C	0.0505692	0.150756	intron-variant	TLE4	GRCh38.p7	9:79678248	GTACCATTCTTTTGT[A/C]ATAATCCTGACTTTA	7091
rs3901861	snp	C/T	0.031825	0.122064	intron-variant	TLE4	GRCh38.p7	9:79677671	AATCTGAGATGGATT[C/T]AATTTTTTTTCTTTT	7091
rs3901862	snp	A/C	0.288127	0.247076	intron-variant	TLE4	GRCh38.p7	9:79678008	TCAGTAGCTTGTTAA[A/C]AAAGCAACTAGTGAG	7091
rs3902070	snp	C/T	0.163564	0.234582	intron-variant	TLE4	GRCh38.p7	9:79677463	TTCTAAGATTTCCTT[C/T]TCTTTTTCTTCAAAA	7091
rs3902071	snp	C/T			intron-variant	TLE4	GRCh38.p7	9:79677659	TGAATTGTGTATAAT[C/T]TGAGATGGATTCAAT	7091
rs3902072	snp	A/G	0.496245	0.0431677	intron-variant	TLE4	GRCh38.p7	9:79677934	TTACCAGGTACTTCT[A/G]GCGTAATTTCTCTCT	7091
rs3902073	snp	A/G	0.496245	0.0431677	intron-variant	TLE4	GRCh38.p7	9:79678052	AAACAAATTCAGTAC[A/G]CTGTTTTATACGTAT	7091
rs3928818	snp	A/G	0.213333	0.247296	intron-variant	TLE4	GRCh38.p7	9:79640670	TCAAAGTAACACTCA[A/G]CTCCTTCTGTTCTTT	7091
rs4011889	in-del	-/AGAC	0.243919	0.249926	intron-variant	TLE4	GRCh38.p7	9:79596631	GCTTTCTTAATTGAG[-/AGAC]AGAAAGAGCCCTAAG	7091
rs4131220	snp	C/T	0.0364509	0.129988	intron-variant	TLE4	GRCh38.p7	9:79633155	AGAGAAGGGAAATTA[C/T]TGCCTCTTAGAGCCT	7091
rs4242612	snp	C/T	0.442791	0.15916	intron-variant	TLE4	GRCh38.p7	9:79623019	TTTTACTACCCCAGT[C/T]AATATGGGGAGTACT	7091
rs4242613	snp	A/G	0.206336	0.246157	intron-variant	TLE4	GRCh38.p7	9:79696917	AAAGAGATTTTTGCC[A/G]ACCCTCTCCACTTTT	7091
rs4298561	snp	C/G	0.5	0	intron-variant	TLE4	GRCh38.p7	9:79679882	atagggaatcctttc[C/G]ccattgcttgttttt	7091
rs4339716	snp	G/T	0.361684	0.223667	intron-variant	TLE4	GRCh38.p7	9:79664534	TGATGATAAAATCTG[G/T]TAGTAACCTAGTCTG	7091
rs4401952	snp	C/T	0.00755907	0.0610114	intron-variant	TLE4	GRCh38.p7	9:79696971	GTACCACATGAGATT[C/T]GCCAGTGAGACTTAG	7091
rs4436200	snp	C/T	0.301429	0.244653	intron-variant	TLE4	GRCh38.p7	9:79636444	ctgtcacataccact[C/T]atgttcttcattcag	7091
rs4492450	snp	C/T	0.495483	0.0473088	intron-variant	TLE4	GRCh38.p7	9:79680028	actgtagccttgtag[C/T]atagtttgaagtcag	7091
rs4877145	snp	A/G	0.492287	0.0616198	intron-variant	TLE4	GRCh38.p7	9:79643386	cattaacacattcct[A/G]taccagtgtgacagc	7091
rs4877146	snp	C/T	0.496681	0.0405994	intron-variant	TLE4	GRCh38.p7	9:79665447	ATTAATGGATCGTTC[C/T]TCTTCATTTCTCAGA	7091
rs4877147	snp	A/T	0.211741	0.247061	intron-variant, upstream-variant-2KB	TLE4	GRCh38.p7	9:79705972	ACTTTAATTTTTTGC[A/T]CTTGCCCAGCCATAT	7091
rs4877497	snp	A/G	0.0614824	0.164198	intron-variant	TLE4	GRCh38.p7	9:79626434	TTCCTTTGGTTCTTC[A/G]TTCACTAAACCAAGT	7091
rs4877500	snp	A/G	0.49263	0.0602539	intron-variant	TLE4	GRCh38.p7	9:79687939	GGCAGTGAGACTGGG[A/G]TTCTGCATTTCTAAC	7091
rs4877501	snp	A/G	0.494936	0.050064	intron-variant	TLE4	GRCh38.p7	9:79688411	TTTGCTTTATGTGGC[A/G]TTCTTGGGCACTTAA	7091
rs5023335	snp	C/G	0.157642	0.232314	intron-variant	TLE4	GRCh38.p7	9:79652255	gcagtggcacgaact[C/G]ggctcactgcaagct	7091
rs5898637	in-del	-/C/CTTC/CTTCTTC			intron-variant	TLE4	GRCh38.p7	9:79592229	TTCTTCTTCTTCTTC[-/C/CTTC/CTTCTTC]TTCCTTCTGCTTCTT	7091
rs5898638	in-del	-/A	0.346368	0.23068	intron-variant	TLE4	GRCh38.p7	9:79624178	AAAACCCGAAAATGG[-/A]AAAAAAAAAAAAAAA	7091
rs5898639	in-del	-/A	0.496314	0.0427728	intron-variant	TLE4	GRCh38.p7	9:79671060	GATTAAATTTTGCCT[-/A]AAAAAAAATCTACAA	7091
rs6151049	in-del	-/ATAGCTATTAAAATGCTGTCTTGTCTAATGTTGAATGATTGTGTAA			intron-variant	TLE4	GRCh38.p7	9:79637091	GCAAGGCTGGAGCTG[lengthTooLong]GCCTATTTATTTTGA	7091
rs6559486	snp	C/T	0.23846	0.249734	intron-variant	TLE4	GRCh38.p7	9:79583438	TGGAGGCAGCTTCTG[C/T]GTTTCACGGAATGAA	7091
rs6559487	snp	C/T	0.24134	0.24985	intron-variant	TLE4	GRCh38.p7	9:79592436	GCTTATCACCACACC[C/T]GGCAATTTTTGTATT	7091
rs6559491	snp	A/T	0.289683	0.24683	intron-variant	TLE4	GRCh38.p7	9:79690077	TCCAACCATGACCCC[A/T]TCCCAGATTTTAAGA	7091
rs6559493	snp	C/G	0.20511	0.245937	intron-variant	TLE4	GRCh38.p7	9:79710760	TCCCTATTCTTTCCT[C/G]TTCTACTACCTTTTT	7091
rs6559494	snp	A/G	0.18989	0.242666	intron-variant	TLE4	GRCh38.p7	9:79722058	TAGTCCCAGCTACTT[A/G]GGAGGCTGTGGCAGG	7091
rs7019624	snp	C/T	0.237014	0.249662	intron-variant	TLE4	GRCh38.p7	9:79644622	TTCTCACACCTAGCC[C/T]GACTTACAGACAGGA	7091
rs7020448	snp	G/T			intron-variant	TLE4	GRCh38.p7	9:79666194	gtgtgtgtgtgtgtg[G/T]gtgggtgGGGTTTTT	7091
rs7022420	snp	A/G	0.16846	0.236329	intron-variant	TLE4	GRCh38.p7	9:79657759	GTGTGCATAATTCCA[A/G]TATCAGGTAGCAAAA	7091
rs7022923	snp	A/G	0.151096	0.229604	intron-variant	TLE4	GRCh38.p7	9:79718085	AGGTAGGCCTTTGGG[A/G]CTGTCAGGATGCCTT	7091
rs7023168	snp	C/T	0.207864	0.246424	intron-variant	TLE4	GRCh38.p7	9:79711197	ACAGTGCTGGCTCCA[C/T]AGCCAAGTTGCTTGG	7091
rs7024523	snp	C/T	0.00159617	0.0282053	intron-variant	TLE4	GRCh38.p7	9:79588338	tatttttagtagaga[C/T]ggggtttcaccatgt	7091
rs7025437	snp	A/G	0.200801	0.245111	intron-variant	TLE4	GRCh38.p7	9:79693755	CATCATGTCCTTCGA[A/G]CCATATTTAGTATTA	7091
rs7029276	snp	G/T	0.148661	0.22854	intron-variant	TLE4	GRCh38.p7	9:79619480	TATGCACTGGTGGAA[G/T]TGTTATCGCCTTACA	7091
rs7029344	snp	A/G			intron-variant	TLE4	GRCh38.p7	9:79582230	CAGTTTTAAATGAAG[A/G]CAGATGTTTTGCTTT	7091
rs7029826	snp	C/T	0.221439	0.248363	intron-variant	TLE4	GRCh38.p7	9:79664627	AATAATGACTAAATA[C/T]GTAAGCGTCCAGGAA	7091
rs7031701	snp	A/C	0.208873	0.246847	intron-variant	TLE4	GRCh38.p7	9:79713059	TATGCTACTTAGAAC[A/C]GAATTTTCTATCGTA	7091

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