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
rs11995	snp	A/G	0.275464	0.2487	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20781764	TTGGACCCTTTCCTC[A/G]CAACTAACTGTCAAC	10529
rs67179	snp	C/T	0.469839	0.119042	intron-variant	NEBL	GRCh38.p7	10:21029963	CTATCATTATACCTA[C/T]AATCATCCCGAGAGA	10529
rs106459	snp	C/G	0.304438	0.244001	intron-variant	NEBL	GRCh38.p7	10:21093259	AGGATAAGTATTTGG[C/G]AAAGACATGAATGGT	10529
rs186377	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21122104	tgggaggtggaggtt[G/T]cagtgagccgagatc	10529
rs188764	snp	C/T	0.484066	0.0878235	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21132343	aaggggtgaatggtg[C/T]tccattgtatagatg	10529
rs191120	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21122095	gaggtttcagtgagc[C/T]gagatcgtgccactg	10529
rs192864	snp	A/G	0.3746	0.216737	intron-variant	NEBL	GRCh38.p7	10:21098671	ACAAGATTGTTACAG[A/G]AGCGCATAAATACAC	10529
rs313787	snp	C/T	0.430285	0.173197	intron-variant	NEBL	GRCh38.p7	10:21097826	CAATAAATGAAGACA[C/T]TGGACTTTTTTATGG	10529
rs313788	snp	A/C	0.23846	0.249734	intron-variant	NEBL	GRCh38.p7	10:21098447	GACTCAGGAAACCCA[A/C]TGGTATTTAATAATT	10529
rs313789	snp	G/T	0.478437	0.10157	intron-variant	NEBL	GRCh38.p7	10:21124701	GTCATAGCTGGAATC[G/T]CAGCACTTTGGGAGG	10529
rs313790	snp	C/T	0.478603	0.101197	intron-variant	NEBL	GRCh38.p7	10:21124380	AGACATTGAAGCTAA[C/T]AATATCTTCTCCTCC	10529
rs313791	snp	C/T	0.461259	0.133677	intron-variant	NEBL	GRCh38.p7	10:21123751	TATATCATCTCAAAC[C/T]AATATATTCATAAAA	10529
rs313792	snp	C/T	0.473174	0.112665	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21144617	tgtaatcccagctac[C/T]tcagaggctgagaca	10529
rs313793	snp	A/G	0.462144	0.132269	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21147793	TTACCTTAGCTACCC[A/G]GCCCCTTCAGCATTC	10529
rs313794	snp	G/T	0.380529	0.213219	intron-variant	NEBL	GRCh38.p7	10:21148979	ttcagaaggggtcct[G/T]ccccatacccaggag	10529
rs313795	snp	A/C	0.380138	0.213458	intron-variant	NEBL	GRCh38.p7	10:21149372	ctcagctcactgcaa[A/C]ctccgcctcctgggt	10529
rs313796	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21149566	aaagtgctgggatta[C/T]aggcatgagccatcg	10529
rs473020	snp	A/G	0.476833	0.105105	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21126884	GGAGGCTAAGGCAGG[A/G]GAATCGCTTGAACCC	10529
rs478559	snp	G/T	0.482309	0.0923707	intron-variant	NEBL	GRCh38.p7	10:21104875	tttttgtagatgccc[G/T]atatcaggatgaaga	10529
rs480272	snp	A/T	0.478603	0.101197	intron-variant	NEBL	GRCh38.p7	10:21105044	tcttttttaaggtta[A/T]gccaaccctgaattc	10529
rs491386	snp	C/T	0.491473	0.0647364	intron-variant	NEBL	GRCh38.p7	10:21052689	GCTCTTCCTGAGTGT[C/T]GGTGATTTCACTGGA	10529
rs494226	snp	C/G	0.460252	0.135255	intron-variant	NEBL	GRCh38.p7	10:21036318	cagaggtgtacacca[C/G]cacgcctggctaatt	10529
rs495866	snp	A/G	0.497182	0.037434	intron-variant	NEBL	GRCh38.p7	10:21042753	CAGGAAGAATCcaga[A/G]gtttgctggtcaatg	10529
rs499364	snp	A/G	0.463126	0.13068	intron-variant	NEBL	GRCh38.p7	10:21048988	gagtctctctctgtc[A/G]tccaggctggagtgc	10529
rs500220	snp	A/G	0.476833	0.105105	intron-variant	NEBL	GRCh38.p7	10:21118103	GTGTCAGTCTGGCTG[A/G]TGCAGCACCCCACAG	10529
rs502246	snp	A/G	0.466204	0.125522	intron-variant	NEBL	GRCh38.p7	10:21163205	TCTGCTAGAAACCCA[A/G]TTTTTTTTCCTATAA	10529
rs508282	snp	A/T	0.463774	0.129618	intron-variant	NEBL	GRCh38.p7	10:21038590	gactggataaagaaa[A/T]tgtggcacatatgca	10529
rs515249	snp	A/C	0.389152	0.207694	intron-variant	NEBL	GRCh38.p7	10:21089156	ACTCCGCTCAAGCAG[A/C]AAACTCAAATGTCCT	10529
rs518712	snp	A/G	0.462472	0.13174	intron-variant	NEBL	GRCh38.p7	10:21035979	acaagcctggccaac[A/G]tggtgaaatcccatt	10529
rs522736	snp	C/T	0.369142	0.219784	intron-variant	NEBL	GRCh38.p7	10:21118210	ACAGGAACATCTCCT[C/T]CAGCTGACAACTTAT	10529
rs524176	snp	A/C	0.302184	0.244493	intron-variant	NEBL	GRCh38.p7	10:21093004	TCTCTGATGTGGGAA[A/C]AGTTTATGACAAGAG	10529
rs525350	snp	A/G	0.495445	0.0475058	intron-variant	NEBL	GRCh38.p7	10:21051250	tggattacaaatgag[A/G]attacaataaAAAAT	10529
rs526061	snp	C/T	0.419456	0.183806	intron-variant	NEBL	GRCh38.p7	10:21025675	tgctcctaTAAGCAC[C/T]GGAATCTGGATAAAA	10529
rs534149	snp	C/T	0.463666	0.129795	intron-variant	NEBL	GRCh38.p7	10:21038005	TCTGAAGAATCTACT[C/T]TTGATTCTGAAATCT	10529
rs534865	snp	C/T	0.463881	0.12944	intron-variant	NEBL	GRCh38.p7	10:21037966	TATGTCTTATGAAGA[C/T]ATTTTTGCTCGTTCT	10529
rs536347	snp	A/T	0	0	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21129121	aattaaaggaatttg[A/T]tgccaatacacctgc	10529
rs543011	snp	A/G	0.463234	0.130503	intron-variant	NEBL	GRCh38.p7	10:21054484	CTGTACTGCCTCTCG[A/G]ACAGGCATCGGGGAA	10529
rs550117	snp	C/G	0.416545	0.186448	intron-variant	NEBL	GRCh38.p7	10:21017393	TTGCTCAAATGTCGT[C/G]TTCTTTAGAAGCAAT	10529
rs561415	snp	A/C	0.460477	0.134905	intron-variant	NEBL	GRCh38.p7	10:21030776	GGCTCAGGTGCAGAT[A/C]TGGAGTCATGCTCCT	10529
rs561753	snp	C/G	0.493523	0.0565391	intron-variant	NEBL	GRCh38.p7	10:21040158	ggatcacgaggtcag[C/G]agattgagaccatcc	10529
rs568929	snp	A/C	0.463451	0.130149	intron-variant	NEBL	GRCh38.p7	10:21053902	GGGATTACAGGTGCG[A/C]ACCACCATGCCTGGC	10529
rs579039	snp	A/G	0.361684	0.223667	intron-variant	NEBL	GRCh38.p7	10:21110398	AACTTCTACATGAAA[A/G]AGAAAAATTTCTTGA	10529
rs579249	snp	C/T	0.49645	0.0419827	intron-variant	NEBL	GRCh38.p7	10:21033929	atccacccgcctcgg[C/T]ctcccaaaatgctgg	10529
rs579640	snp	C/T	0.474091	0.11083	intron-variant	NEBL	GRCh38.p7	10:21153299	AGGGCCTTTGCAGCC[C/T]TGCTGTATAGTGTGG	10529
rs581366	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21153461	cagcctcctgaatag[A/C]tgggattacaggtgc	10529
rs587211	snp	C/T	0.493703	0.0557558	intron-variant	NEBL	GRCh38.p7	10:21039634	aaagttttaaaaaca[C/T]CATTTTAAGTTATGT	10529
rs589425	snp	A/G	0.460589	0.13473	intron-variant	NEBL	GRCh38.p7	10:21033514	AAAACTTAAATCTCT[A/G]TCACTCTCAAAATTC	10529
rs589483	snp	A/C	0.463451	0.130149	intron-variant	NEBL	GRCh38.p7	10:21040120	cacctgcaatcccag[A/C]actttgggaggctga	10529
rs590763	snp	A/G	0.460702	0.134554	intron-variant	NEBL	GRCh38.p7	10:21033827	TATATTGAGAGCCAA[A/G]CGAGAGCCATATCAT	10529
rs590767	snp	C/G	0.195214	0.243923	intron-variant	NEBL	GRCh38.p7	10:21036987	AGGTGGGAACAGCTA[C/G]GGTGGAGAACCTCTG	10529
rs591652	snp	C/T	0.35809	0.225425	intron-variant	NEBL	GRCh38.p7	10:21118004	ATTGAACATCACTCC[C/T]AGCACAGAATAATTA	10529
rs594599	snp	A/G	0.463234	0.130503	intron-variant	NEBL	GRCh38.p7	10:21053577	AAAATAAGCCTACCC[A/G]TTGGATTCTTTATAA	10529
rs597837	snp	A/C	0.431473	0.171952	intron-variant	NEBL	GRCh38.p7	10:21013892	AAACAAAAAGAACCC[A/C]ATGAAGAGCAGAGTC	10529
rs599087	snp	A/G	0.257176	0.249897	intron-variant	NEBL	GRCh38.p7	10:21007590	GGCACAATATCATCC[A/G]GGCGATTGCTTAGTG	10529
rs600402	snp	C/G	0.378372	0.214524	intron-variant	NEBL	GRCh38.p7	10:21117064	AATATTGCTGAGCTT[C/G]AGCTGGGTGCAATAA	10529
rs602053	snp	A/G	0.47517	0.10862	intron-variant	NEBL	GRCh38.p7	10:21053774	AAGTGCTGGGATTAC[A/G]GATTTGAGCCACCAT	10529
rs602572	snp	A/G	0.477345	0.103991	intron-variant	NEBL	GRCh38.p7	10:21110940	cacaagcattcctat[A/G]cagcaataacagaca	10529
rs603346	snp	A/G	0.463126	0.13068	intron-variant	NEBL	GRCh38.p7	10:21053519	TTATCTTTTTCCTTA[A/G]CTACTGATGCTCATT	10529
rs603790	snp	C/T	0.497329	0.0364438	intron-variant	NEBL	GRCh38.p7	10:21053419	ATCATAGATAATATT[C/T]TTGCCTGTTTCCTTT	10529
rs604251	snp	C/T	0.460813	0.134379	intron-variant	NEBL	GRCh38.p7	10:21034494	GCTTATCCTGTGCTC[C/T]AGGATGTCTGGCAAC	10529
rs604600	snp	C/T	0.0295035	0.117819	intron-variant	NEBL	GRCh38.p7	10:21163995	TCCTTCTCACAACTT[C/T]CTGTTTTCATGGTTA	10529
rs605715	snp	C/T	0.465578	0.126594	intron-variant	NEBL	GRCh38.p7	10:21088937	GCAGTTAATGAACCA[C/T]GCGAGGCAGGAAAGA	10529
rs608788	snp	C/T	0.279726	0.248226	intron-variant	NEBL	GRCh38.p7	10:20999992	TTTCCAGCAATGTAG[C/T]CATTTACTACAAAGC	10529
rs611992	snp	G/T	0.491473	0.0647364	intron-variant	NEBL	GRCh38.p7	10:21048509	AGATTTAGCACCACA[G/T]GAGTTTTAAAAATAT	10529
rs613306	snp	C/G	0.497387	0.0360476	intron-variant	NEBL	GRCh38.p7	10:21048787	gatcaccttaggtca[C/G]gagtacgagaccagc	10529
rs613407	snp	C/T	0.4628	0.13121	intron-variant	NEBL	GRCh38.p7	10:21048865	aaaaataaaattagc[C/T]gggcatggtggcagg	10529
rs618568	snp	C/G	0.315273	0.241329	intron-variant	NEBL	GRCh38.p7	10:21035401	AGCATTGTGTACAAC[C/G]TTGTCAACTACTGTG	10529
rs620853	snp	A/G	0.462253	0.132093	intron-variant	NEBL	GRCh38.p7	10:21035891	AAAAGggctgggcac[A/G]gtagcttaggcctgt	10529
rs621429	snp	A/G	0.4021	0.198407	intron-variant	NEBL	GRCh38.p7	10:21087760	TCTCAATTATACCGA[A/G]GTCAGGGCTGCAAAC	10529
rs623047	snp	A/G	0.460813	0.134379	intron-variant	NEBL	GRCh38.p7	10:21034468	GCAACAGGTGCCTGC[A/G]TTACTGTGCTGAGAA	10529
rs623551	snp	A/T	0.460925	0.134204	intron-variant	NEBL	GRCh38.p7	10:21034311	AATTGTGGAAAACTA[A/T]TAATTAACAATAAAA	10529
rs623634	snp	C/G	0.077417	0.180873	intron-variant	NEBL	GRCh38.p7	10:21166113	CCTGCCTCAGCCTCC[C/G]GAGTAGCTGGGACTT	10529
rs625223	snp	C/G	0.481757	0.0937492	missense, intron-variant, utr-variant-3-prime	C10orf113, NEBL	GRCh38.p7	10:21125963	CCCAGTTGCCTGGAT[C/G]TGGTTCAGGAGCTGC	10529
rs625903	snp	A/G	0.483272	0.0899109	intron-variant	NEBL	GRCh38.p7	10:21151499	TGCTTTATTTTTACA[A/G]CCAGCCAAAGTGAAA	10529
rs627000	snp	A/G	0.478685	0.10101	intron-variant	NEBL	GRCh38.p7	10:21108458	ttgttcagtttccac[A/G]tagttgtgcgctttt	10529
rs627340	snp	C/T	0.463234	0.130503	intron-variant	NEBL	GRCh38.p7	10:21108499	attaatcctgagttc[C/T]aatttgattgcactg	10529
rs631361	snp	A/G	0.496905	0.0392151	intron-variant	NEBL	GRCh38.p7	10:21047073	AAAGTCTGCATGGCA[A/G]TAACATTCATCACAT	10529
rs632551	snp	G/T	0.309154	0.242901	intron-variant	NEBL	GRCh38.p7	10:21101341	TCATGCCCAGATCAC[G/T]TGCAGGCAATGTGGT	10529
rs633714	snp	A/G	0.461148	0.133852	intron-variant	NEBL	GRCh38.p7	10:21043090	TATACAGCTCTTCTA[A/G]AGACTTAAATCTGAC	10529
rs634567	snp	A/G	0.314301	0.241589	intron-variant	NEBL	GRCh38.p7	10:21043307	GTCATCCTACAAAAA[A/G]ACAGCCGTCAACATT	10529
rs634614	snp	C/T	0.462909	0.131034	intron-variant	NEBL	GRCh38.p7	10:21036769	TGCTCAGGCGGATGG[C/T]TCACTTTCTGTAGAG	10529
rs634878	snp	C/G	0.490508	0.0682328	intron-variant	NEBL	GRCh38.p7	10:21087491	CTTTTTTCAGACTTT[C/G]TCTTCTCCCAGTTTT	10529
rs637189	snp	G/T	0	0	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21143150	ATGTTCAAAGGGAGG[G/T]TAAACTTTAAGCATG	10529
rs638548	snp	C/G	0.460702	0.134554	intron-variant	NEBL	GRCh38.p7	10:21033238	TTGATATTTTTCAGA[C/G]TATACTCATATCTTA	10529
rs638597	snp	A/G	0.170408	0.236992	intron-variant	NEBL	GRCh38.p7	10:21033200	GAGTCCCAAATCTGC[A/G]TGTGTTTCTCTTGGC	10529
rs638929	snp	G/T	0.460252	0.135255	intron-variant	NEBL	GRCh38.p7	10:21029696	CAATACCCACGGCCA[G/T]ACTGGTCTGAATCAT	10529
rs640056	snp	C/T	0.371177	0.218669	intron-variant	NEBL	GRCh38.p7	10:21002402	AGTTATCCTACGCTG[C/T]AGAATGTTTACCATG	10529
rs640729	snp	C/T	0.46014	0.13543	intron-variant	NEBL	GRCh38.p7	10:21030071	CAAAATAAGCTCGAC[C/T]GGACTGGGAGGTACT	10529
rs640750	snp	G/T	0.459914	0.13578	intron-variant	NEBL	GRCh38.p7	10:21030081	CCTCCAAAGACAAAA[G/T]AAGCTCGACCGGACT	10529
rs641632	snp	G/T	0.459801	0.135955	intron-variant	NEBL	GRCh38.p7	10:21040496	cttctctcctctatt[G/T]ctccttcgctcacca	10529
rs642446	snp	A/T	0.438246	0.16451	intron-variant	NEBL	GRCh38.p7	10:21013702	GGCCAACATGGTGAA[A/T]CCCCATCTCTACTAA	10529
rs643674	snp	G/T	0.462909	0.131034	intron-variant	NEBL	GRCh38.p7	10:21049666	AAGTGAGGAACGGGG[G/T]CAGGGTGGGCGGTTG	10529
rs649597	snp	G/T	0.304688	0.243945	intron-variant	NEBL	GRCh38.p7	10:21088438	GTAGTGGGCTATGAT[G/T]GTACCACTGCACTCC	10529
rs649734	snp	C/T	0.464096	0.129085	intron-variant	NEBL	GRCh38.p7	10:21037791	GGGAGTGTTTTTTGA[C/T]CTCCAATTTATCTTG	10529
rs652864	snp	A/G	0.460027	0.135605	intron-variant	NEBL	GRCh38.p7	10:21030470	TTACCTTTTGGGGCT[A/G]ATCAGTTTTGGTAGA	10529
rs653028	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21111945	tgtcttcctttgaga[A/G]gtgtttgttcatatc	10529
rs653038	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21111940	tcctttgagaagtgt[C/T]tgttcatatcctttc	10529
rs654278	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21039995	CAAAAATATTCTCTG[C/G]CTGTGTAATCCTATG	10529
rs654355	snp	C/G	0	0	intron-variant	NEBL	GRCh38.p7	10:21030860	GTACAGGTGTTAAGT[C/G]GTTTGAATACCACCC	10529
rs654717	snp	A/G	0.460589	0.13473	intron-variant	NEBL	GRCh38.p7	10:21030903	TCTGATCTTTCAGAT[A/G]CCATTTTTGATTGGT	10529

Full records

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