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
rs11893	snp	A/C	0.188	0.24219	utr-variant-3-prime	BTBD11	GRCh38.p7	12:107659442	GGAGGAAGGTGACAG[A/C]CGCAATGCACACGCT	121551
rs15607	snp	G/T	0.0198	0.0975087	utr-variant-3-prime	BTBD11	GRCh38.p7	12:107659546	AAATCAATGCCTGGA[G/T]GCCCTGAACTAGCAT	121551
rs703685	snp	A/C	0.00438332	0.0466095	intron-variant	BTBD11	GRCh38.p7	12:107324561	CTACCTTTAGTGAAG[A/C]GGCACCAGGAAACTT	121551
rs703686	snp	A/G	0.0260105	0.111035	intron-variant	BTBD11	GRCh38.p7	12:107325210	CTCACCTGTCAGCAC[A/G]GGCTTGGAGGGTAGG	121551
rs713459	snp	A/G	0.196149	0.244131	intron-variant	BTBD11	GRCh38.p7	12:107562593	CTACAGGTCCCCTTA[A/G]GCCTGCAAAGGGACC	121551
rs718585	snp	G/T	0.474634	0.109726	intron-variant	BTBD11	GRCh38.p7	12:107324505	TAAAATAAAATTAAG[G/T]TAGCTTATTTTATTT	121551
rs724996	snp	A/C	0.202343	0.245416	intron-variant	BTBD11	GRCh38.p7	12:107571761	TTCCTGCCACAGAGG[A/C]CTCTGCCTTCCTTAA	121551
rs731066	snp	C/G	0.364817	0.222075	intron-variant	BTBD11	GRCh38.p7	12:107475207	TTCCTTACCTCGAGT[C/G]CAGGGAGATATTGTC	121551
rs732750	snp	A/C	0.323434	0.238972	intron-variant	BTBD11	GRCh38.p7	12:107509954	AACCTGGCACAGAGA[A/C]GGGAGTCGATAAATG	121551
rs734544	snp	C/G	0.211212	0.246973	intron-variant	BTBD11	GRCh38.p7	12:107419106	TAAACTCCCCTGGGG[C/G]TATGCAACCTCATGA	121551
rs741366	snp	A/T	0.323671	0.238899	intron-variant	BTBD11	GRCh38.p7	12:107511318	GGAGGTAGTTTGTTA[A/T]GCTGCATATGCACAA	121551
rs741367	snp	C/T	0.480302	0.0972668	intron-variant	BTBD11	GRCh38.p7	12:107648819	TGCGCGGAACTGCTG[C/T]ACACGTGGCATGGCT	121551
rs741404	snp	A/G	0.495634	0.0465208	intron-variant	BTBD11	GRCh38.p7	12:107341385	CCTGGACAGCCTCAC[A/G]GGGTTGGGGCAGTGG	121551
rs741405	snp	C/T	0.496517	0.0415876	intron-variant	BTBD11	GRCh38.p7	12:107341456	CCATGGAACCCTGCA[C/T]TCTCTTTCTTCTTAC	121551
rs749137	snp	A/G	0.394721	0.203852	intron-variant	BTBD11	GRCh38.p7	12:107408120	AATAAAACCCCAAGC[A/G]GATGCTAAAAATGTG	121551
rs749138	snp	C/T	0.393987	0.204372	intron-variant	BTBD11	GRCh38.p7	12:107408154	GGCTTTGTGAGGAGA[C/T]AGGCGTGCTCTGTGT	121551
rs749139	snp	G/T	0	0	intron-variant	BTBD11	GRCh38.p7	12:107408405	TGTCAGGAAATGGTT[G/T]AAACACCCAGTATGA	121551
rs749837	snp	C/T	0.293551	0.246177	intron-variant	BTBD11	GRCh38.p7	12:107512068	TATGGAGTTAGTTTT[C/T]CTTTACCAGTAGTTA	121551
rs753792	snp	C/T	0.143959	0.226396	intron-variant	BTBD11	GRCh38.p7	12:107511343	GTTGATGTTTTAAGC[C/T]GCTGAATTTGGAGGT	121551
rs759519	snp	C/T	0.466515	0.124985	intron-variant, upstream-variant-2KB	BTBD11	GRCh38.p7	12:107520047	GGCTCACTTTGTTTG[C/T]TCAACAGATCTAGCT	121551
rs759520	snp	C/T	0.466824	0.124448	intron-variant, upstream-variant-2KB	BTBD11	GRCh38.p7	12:107519515	GCCTGGCCAACATGG[C/T]GAAACACCGTCTCTA	121551
rs759521	snp	G/T	0.141596	0.225274	intron-variant	BTBD11	GRCh38.p7	12:107510675	catcggcttcccaaa[G/T]tgctgggattccttt	121551
rs759522	snp	C/T	0.472709	0.11358	intron-variant	BTBD11	GRCh38.p7	12:107510438	TTCCCTGTGTGGGGG[C/T]GGTTATGGTGTAGCA	121551
rs759524	snp	A/G	0.347032	0.230401	intron-variant	BTBD11	GRCh38.p7	12:107644514	ACCCCACCCTTCTCC[A/G]GGTATTCTGAGAGCT	121551
rs759525	snp	A/G	0.382085	0.212258	intron-variant	BTBD11	GRCh38.p7	12:107644426	ttgggataccgggag[A/G]aggtgggggagaccg	121551
rs759564	snp	A/G	0.312104	0.242163	intron-variant	BTBD11	GRCh38.p7	12:107334899	TGGTCCCTTGCATCA[A/G]GTGGTATTTGAGGTA	121551
rs856886	snp	C/T	0.432504	0.170857	intron-variant	BTBD11	GRCh38.p7	12:107331926	TGGGTCCGCTGGCTG[C/T]TCTCGCTGATTCGGC	121551
rs856887	snp	A/G	0.223522	0.248594	intron-variant	BTBD11	GRCh38.p7	12:107332037	GCCTCTGATGGCCCC[A/G]TAATGTGGAGCCTCG	121551
rs856888	snp	C/T	0.330714	0.236612	intron-variant	BTBD11	GRCh38.p7	12:107332502	ATCCCTGGTTCTCGG[C/T]GCCTGTTCCTAACCA	121551
rs856889	snp	C/T	0.345925	0.230864	intron-variant	BTBD11	GRCh38.p7	12:107334593	ggaggacatgttaac[C/T]aggccattggatact	121551
rs856890	snp	A/G	0.347032	0.230401	intron-variant	BTBD11	GRCh38.p7	12:107341913	ACATGCCTGCTCCCC[A/G]CTCACCTTCTGCCAT	121551
rs856891	snp	C/T	0.351635	0.228408	intron-variant	BTBD11	GRCh38.p7	12:107343077	TGGAGTGCAGGGGCA[C/T]GATCATGGCTCACTG	121551
rs856892	snp	C/T	0.34659	0.230587	intron-variant	BTBD11	GRCh38.p7	12:107347164	CTGTATTTACTGAAG[C/T]AGTCCTCCTAACTTG	121551
rs867176	snp	A/C	0.444	0.157683	intron-variant	BTBD11	GRCh38.p7	12:107340750	AAAGAAACAAACAAA[A/C]CCTCCTGGGAAATTC	121551
rs882027	snp	C/T	0.492188	0.0620098	intron-variant	BTBD11	GRCh38.p7	12:107539793	ACTTAACCTCTCAGG[C/T]GAGGAATAATCTTCA	121551
rs882028	snp	A/G	0.367708	0.220556	intron-variant	BTBD11	GRCh38.p7	12:107539408	AGGAAGCTAAGCTGG[A/G]TGCCTGCCTCCGGGC	121551
rs885721	snp	A/G	0.488786	0.0740357	intron-variant	BTBD11	GRCh38.p7	12:107340462	AAACAAAACCAAACA[A/G]TGAGCCTTCTCCCAT	121551
rs888154	snp	G/T	0.490287	0.0690083	intron-variant	BTBD11	GRCh38.p7	12:107540405	GGGCTGAGTGAGGAA[G/T]ACCTGTCCTCACCCA	121551
rs888155	snp	A/C	0.491525	0.0645418	intron-variant	BTBD11	GRCh38.p7	12:107540178	GGCTGGCATCTTGAT[A/C]TTGAACTTCCCAGCC	121551
rs888156	snp	A/T	0.208779	0.246578	intron-variant	BTBD11	GRCh38.p7	12:107540129	TACATTTCTGTTCTT[A/T]ATAAATCCTCCAGTC	121551
rs888157	snp	C/T	0.492087	0.0623997	intron-variant	BTBD11	GRCh38.p7	12:107540066	TAACGCAGGGGGTTA[C/T]ATCCCTACATCTCTC	121551
rs888158	snp	A/G	0.174288	0.23826	intron-variant	BTBD11	GRCh38.p7	12:107538514	GAGCTGCTCCCTGAA[A/G]GCTATGAAAAGTTGG	121551
rs918094	snp	C/T	0	0	intron-variant	BTBD11	GRCh38.p7	12:107564021	TTTTCATGATAATTT[C/T]CTGATTCCAGTTTCT	121551
rs918095	snp	A/C	0.00478085	0.0486577	intron-variant	BTBD11	GRCh38.p7	12:107603509	ctgcatgtggatatc[A/C]agtttccccaaagcc	121551
rs933878	snp	C/G	0.00484259	0.0489678	intron-variant	BTBD11	GRCh38.p7	12:107366165	AAAGGTTCAAAGAGG[C/G]ACAAAGCAAAAAGGG	121551
rs933879	snp	A/G	0.427271	0.176281	intron-variant	BTBD11	GRCh38.p7	12:107367724	CGAGCTCAGGAGTTC[A/G]AGACTGCCCTGGGCA	121551
rs933880	snp	A/G	0.493013	0.058691	intron-variant	BTBD11	GRCh38.p7	12:107454875	TGACACATACCAAAG[A/G]CTGAGTAATTAGCAC	121551
rs933881	snp	C/T	0.476052	0.106772	intron-variant	BTBD11	GRCh38.p7	12:107375721	ATCACAGAAACCAAG[C/T]AGTAAGGAACCTCAG	121551
rs934087	snp	A/T			intron-variant	BTBD11	GRCh38.p7	12:107598337	caagccagcaagatc[A/T]ggcttcagctcacca	121551
rs957626	snp	G/T	0.153	0.230415	intron-variant	BTBD11	GRCh38.p7	12:107586164	TTAAAGCAGGAGCAT[G/T]ACCCTGTCCCTGCCC	121551
rs957627	snp	C/G	0.454061	0.144427	intron-variant	BTBD11	GRCh38.p7	12:107586142	TCCCTGCCCCTGCAA[C/G]GTCCTGAGGAGCTCT	121551
rs957628	snp	A/G	0.452597	0.146474	intron-variant	BTBD11	GRCh38.p7	12:107585976	CCTCAGTGACATTTA[A/G]GTCCTGGGCACTCCA	121551
rs961498	snp	C/G	0.499224	0.0196847	missense, upstream-variant-2KB	BTBD11	GRCh38.p7	12:107319734	GCTGCAGTGGCCCTG[C/G]GTCAGGCTCGGGCTC	121551
rs979321	snp	A/G	0.174288	0.23826	intron-variant	BTBD11	GRCh38.p7	12:107522573	GGAGAGAGAGAGAGA[A/G]ACAATTAAAAAAATA	121551
rs1002256	snp	A/T			intron-variant	BTBD11	GRCh38.p7	12:107403094	CATTCATTCCGATTG[A/T]GAGAATACCCtttaa	121551
rs1002257	snp	A/T			intron-variant	BTBD11	GRCh38.p7	12:107403096	TTCATTCCGATTGAG[A/T]GAATACCCtttaatg	121551
rs1002923	snp	C/T	0.0360663	0.129354	intron-variant, upstream-variant-2KB	BTBD11	GRCh38.p7	12:107414266	ATCCTAGTGGGGGCT[C/T]CGAATACACTGTGTG	121551
rs1006191	snp	C/G	0.44651	0.154543	intron-variant	BTBD11	GRCh38.p7	12:107493829	TTGCTGGCAATGCTT[C/G]GCATTTCCTGGTTGT	121551
rs1077275	snp	A/G	0.237593	0.249692	intron-variant	BTBD11	GRCh38.p7	12:107402371	CTCAGCCTCTTAGGC[A/G]GTCAAGCCAGATTTG	121551
rs1107438	snp	A/G	0.432797	0.170544	utr-variant-5-prime, upstream-variant-2KB	BTBD11	GRCh38.p7	12:107318663	TTGGAAGAAAGGGGC[A/G]AGCCCCGGCGGGAGC	121551
rs1123666	snp	A/G	0.41023	0.191902	intron-variant	BTBD11	GRCh38.p7	12:107493997	CCAAGCACTGTCATA[A/G]CAAAGTTCTACACTT	121551
rs1123667	snp	C/T	0.447162	0.153712	intron-variant	BTBD11	GRCh38.p7	12:107493988	GTCATAACAAAGTTC[C/T]ACACTTACTGGCTTA	121551
rs1344611	snp	A/G	0	0	intron-variant	BTBD11	GRCh38.p7	12:107357181	AATGCTGGGCAAACA[A/G]ATAAGTGGCATTTGC	121551
rs1346202	snp	C/T	0.4711	0.116682	intron-variant	BTBD11	GRCh38.p7	12:107401499	ACAGGGGGTCAGTCA[C/T]TGCCCAAGGTTTCAG	121551
rs1346203	snp	C/G	0.45946	0.136478	intron-variant	BTBD11	GRCh38.p7	12:107401561	ACAGTAGTGAGTGCT[C/G]CCATGATGCAAAATG	121551
rs1346204	snp	C/G	0.496778	0.0400063	intron-variant	BTBD11	GRCh38.p7	12:107395777	AGGGACAGAGCGTGG[C/G]AGAAGGGAGGCAGCT	121551
rs1346205	snp	C/T	0.45692	0.1403	intron-variant	BTBD11	GRCh38.p7	12:107395722	ATAAGTGACCAGAGC[C/T]GGCCCCCACTGGGGG	121551
rs1346206	snp	A/G	0.384593	0.210677	intron-variant	BTBD11	GRCh38.p7	12:107395674	GCACCTGGGGAGCGT[A/G]GCCAAGTTGGGAGTC	121551
rs1346207	snp	A/G	0.389903	0.207189	intron-variant	BTBD11	GRCh38.p7	12:107392256	AGTTTGGCAGGCTGG[A/G]AGAGCAGGGAAGCCC	121551
rs1365347	snp	C/T	0.358515	0.225221	intron-variant	BTBD11	GRCh38.p7	12:107507405	TGCACTGGTCTGGGT[C/T]TGCTGGCAGCCCGAG	121551
rs1365348	snp	A/G	0.209084	0.246629	intron-variant	BTBD11	GRCh38.p7	12:107507519	GAATCCTGACTTCAC[A/G]CAGGCACCAGAATTG	121551
rs1365349	snp	A/G	0.184838	0.241358	intron-variant	BTBD11	GRCh38.p7	12:107507755	GTTCCCTCCAGTTTG[A/G]ACTTCCCTATGCCCT	121551
rs1365350	snp	C/T	0.209693	0.246729	intron-variant	BTBD11	GRCh38.p7	12:107507785	TCCTCTTCCCCACCC[C/T]CTAGCCAGGTCACCT	121551
rs1365351	snp	C/T	0.364401	0.222289	intron-variant	BTBD11	GRCh38.p7	12:107478715	GGGTTTCAAGCTCCC[C/T]GCACGTGAAATATAC	121551
rs1420735	snp	C/T	0.309154	0.242901	intron-variant	BTBD11	GRCh38.p7	12:107595140	TAGGAACAAAATCCA[C/T]CTTTTTTCCAAAGTC	121551
rs1420736	snp	C/T	0.452227	0.146984	intron-variant	BTBD11	GRCh38.p7	12:107594371	TAAAACAAGTGATTC[C/T]AAGTCCTCCTCCCTG	121551
rs1420737	snp	A/G	0.457504	0.139435	intron-variant	BTBD11	GRCh38.p7	12:107642823	CATGAACTCCCCCCA[A/G]ACAGAAGGAGAAATG	121551
rs1420738	snp	A/G	0.314787	0.241459	intron-variant	BTBD11	GRCh38.p7	12:107642669	AAGTTTTGGGACTTC[A/G]CACATGCTGTTCTCT	121551
rs1420739	snp	A/G	0.314787	0.241459	intron-variant	BTBD11	GRCh38.p7	12:107642482	AGTACTCTACTGTAT[A/G]CTGTAATTGACCAAT	121551
rs1420740	snp	C/T	0.480302	0.0972668	intron-variant	BTBD11	GRCh38.p7	12:107642455	CAATTACTCAGTCAC[C/T]GTCCCCGCCCCCCAC	121551
rs1420741	snp	A/G	0.117537	0.212022	intron-variant	BTBD11	GRCh38.p7	12:107627345	ATTTTCATTAGATCC[A/G]TGTCCAGGCTTAAGT	121551
rs1420742	snp	C/T	0.284471	0.247612	intron-variant	BTBD11	GRCh38.p7	12:107623912	ACTTCCTGACCGTTT[C/T]GTCTAAGTTAGACCT	121551
rs1420743	snp	C/T	0.110167	0.207236	intron-variant	BTBD11	GRCh38.p7	12:107623606	GTCGAGGCAAGTAGA[C/T]CACCTGAGGTCAGGA	121551
rs1420744	snp	C/T	0.293037	0.246268	intron-variant	BTBD11	GRCh38.p7	12:107614494	GATTCTCAGTGGTGG[C/T]AAACCCCAGGCAAGG	121551
rs1426453	snp	A/C	0.409382	0.192607	upstream-variant-2KB, utr-variant-5-prime	BTBD11	GRCh38.p7	12:107318157	CCCTCCGGGAGAATG[A/C]GGGCAGGGACAGCAG	121551
rs1426454	snp	C/T	0.363568	0.222716	upstream-variant-2KB, utr-variant-5-prime	BTBD11	GRCh38.p7	12:107318251	CACTTCCTGCAGCCT[C/T]GGTGTCCGCCGGGGG	121551
rs1426455	snp	C/T	0.406468	0.194981	intron-variant	BTBD11	GRCh38.p7	12:107321632	ACACACACACACACA[C/T]CCTGAAATATCGACT	121551
rs1426456	snp	G/T	0.47614	0.106587	intron-variant	BTBD11	GRCh38.p7	12:107324217	TAATTCATTCCCACA[G/T]GCTTAGGGTGGATGG	121551
rs1426457	snp	C/T	0.475702	0.107512	intron-variant	BTBD11	GRCh38.p7	12:107324221	TCATTCCCACATGCT[C/T]AGGGTGGATGGAGCC	121551
rs1426458	snp	A/G	0.473451	0.112115	intron-variant	BTBD11	GRCh38.p7	12:107328181	ccttacaaagcaggc[A/G]ctattattatcccca	121551
rs1426459	snp	A/G	0.404907	0.196224	intron-variant	BTBD11	GRCh38.p7	12:107357821	TCCTATTAGGGCCTC[A/G]CAGGGCAGACCAGAG	121551
rs1426460	snp	A/C	0.364817	0.222075	intron-variant	BTBD11	GRCh38.p7	12:107478183	CCCTGTGCTAAATGG[A/C]CTGACACAATTGTAG	121551
rs1426461	snp	A/G	0.364609	0.222182	intron-variant	BTBD11	GRCh38.p7	12:107477091	ATTTTCAGACACAGG[A/G]CACAGACATTTTAAT	121551
rs1426462	snp	C/T	0.442113	0.159977	intron-variant	BTBD11	GRCh38.p7	12:107393106	CCTACGTATAAATCA[C/T]TGGCTTCTTCAGCGG	121551
rs1426463	snp	A/G	0.44546	0.155869	intron-variant	BTBD11	GRCh38.p7	12:107392856	ACTCTTTACAAAATC[A/G]CCAGAAAAAGATTAA	121551
rs1426464	snp	A/G	0.480461	0.0968913	intron-variant	BTBD11	GRCh38.p7	12:107389798	CTCACACTTGCAACC[A/G]TCTTCCACCAAGGCA	121551
rs1426465	snp	A/G/T	0.000399281	0.0141238	intron-variant	BTBD11	GRCh38.p7	12:107385145	AGGAGACAATAAAAA[A/G/T]AATGAATGAATGGCT	121551
rs1426466	snp	A/G	0.417845	0.185278	intron-variant	BTBD11	GRCh38.p7	12:107378790	AGGGGACGTTTTCAC[A/G]AGTGACAGAAGATCC	121551
rs1426467	snp	C/G	0.140919	0.224948	intron-variant	BTBD11	GRCh38.p7	12:107378471	GCCTCAGATCCTCAT[C/G]TATAAAATAGGACAG	121551
rs1468846	snp	G/T	0.209084	0.246629	intron-variant	BTBD11	GRCh38.p7	12:107570754	GGAGGAGCAGACAGG[G/T]AGGGCCTGCAACTTC	121551

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