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
rs14496	snp	C/T	0.0150606	0.0854603	utr-variant-3-prime, downstream-variant-500B, intron-variant	LDB2, LOC105374505	GRCh38.p7	4:16501604	CCGTGTGTTAAAAAA[C/T]AGCTGTATTTTATGT	9079
rs49969	snp	C/T	0.474363	0.110278	intron-variant	LDB2	GRCh38.p7	4:16830189	gtctccccatccaaa[C/T]ctcatctccaattgt	9079
rs108720	snp	A/G	0.432063	0.171327	intron-variant	LDB2	GRCh38.p7	4:16762921	TCTGCCAAAACTCAC[A/G]TATGTATGTAGGCCC	9079
rs114429	snp	C/T	0.472709	0.11358	intron-variant	LDB2	GRCh38.p7	4:16841157	TAACTGAATCTTTTT[C/T]TACAGGGGTAAGAAA	9079
rs114430	snp	C/T	0.478188	0.10213	intron-variant	LDB2	GRCh38.p7	4:16841057	ATCAAAACACAATTT[C/T]ACAGGTTATGAGTTT	9079
rs123043	snp	G/T	0.479258	0.0997024	intron-variant	LDB2	GRCh38.p7	4:16822277	CTGCTTTAACCAATG[G/T]TCTATTAGCCTACCT	9079
rs149367	snp	A/G	0.00318978	0.0398085	intron-variant	LDB2	GRCh38.p7	4:16634287	ttttttggccgtgca[A/G]aagactttagtttaa	9079
rs150121	snp	A/G			intron-variant	LDB2	GRCh38.p7	4:16752783	atgttaggcatgtga[A/G]atgacattagacatg	9079
rs150260	snp	A/G	0.329783	0.236927	intron-variant	LDB2	GRCh38.p7	4:16775552	tgatggataacaatt[A/G]ttgatgcttactgca	9079
rs150261	snp	A/C	0.409212	0.192748	intron-variant	LDB2	GRCh38.p7	4:16806879	AGGCTGTGTTATTAG[A/C]ACTATTGTGTAGATG	9079
rs157482	snp	A/G	0.360842	0.224085	intron-variant	LDB2	GRCh38.p7	4:16763304	AACTCAGCTCGGGAA[A/G]TCACTTTACAAAGTT	9079
rs157483	snp	C/T	0.43221	0.171171	intron-variant	LDB2	GRCh38.p7	4:16762576	gtgcgttagttctca[C/T]gagatctgatggttt	9079
rs157484	snp	G/T	0.4582	0.138394	intron-variant	LDB2	GRCh38.p7	4:16699825	GTGCCTCAGAGGGAC[G/T]AGAATTCCCATAATG	9079
rs157485	snp	A/G	0.457853	0.138915	intron-variant	LDB2	GRCh38.p7	4:16705372	ATGTGACATTTTTTG[A/G]CTAAGGGAAAGTGGA	9079
rs157486	snp	G/T	0.324855	0.23853	intron-variant	LDB2	GRCh38.p7	4:16709641	TTTGATTTGCACATT[G/T]TCTTTCTAAATATTG	9079
rs157606	snp	C/T	0.495252	0.0484902	intron-variant	LDB2	GRCh38.p7	4:16698172	TATTTACCCAGTTTC[C/T]TGTTGACAAATCATT	9079
rs157607	snp	A/G	0.485255	0.0845871	intron-variant	LDB2	GRCh38.p7	4:16698898	AATTCCTAAAGTCTC[A/G]GCAATCAAAGGTCTT	9079
rs157608	snp	C/T	0.494896	0.0502606	intron-variant	LDB2	GRCh38.p7	4:16698924	GTCTTTTGAAGAAAA[C/T]AAGGAAAAGTTTTGA	9079
rs157609	snp	A/G	0.330016	0.236849	intron-variant	LDB2	GRCh38.p7	4:16699581	ATGGAGAATATGTGA[A/G]GTGGAGAAGTATATA	9079
rs157610	snp	A/G	0.495056	0.049474	intron-variant	LDB2	GRCh38.p7	4:16699679	TCAAAAATAAAAACT[A/G]TAGAGAAAAGGAAGA	9079
rs157611	snp	A/G	0.358303	0.225323	intron-variant	LDB2	GRCh38.p7	4:16779557	GAGTGGGAAGACACG[A/G]GGTGAGTAACCTGGA	9079
rs157612	snp	A/G	0.447032	0.153878	intron-variant	LDB2	GRCh38.p7	4:16775476	tctcatagtagcact[A/G]tgaggtagctacact	9079
rs157613	snp	A/G	0.2768	0.248559	intron-variant	LDB2	GRCh38.p7	4:16776664	atccgctagtataca[A/G]ggtcttcaaggacgt	9079
rs157614	snp	C/T	0.328616	0.237317	intron-variant	LDB2	GRCh38.p7	4:16707277	ACTACTATCTTTCTA[C/T]TATACACATTTTGGC	9079
rs157615	snp	C/T	0.499879	0.0077866	intron-variant	LDB2	GRCh38.p7	4:16708810	TCTCTGTGGGAGCTA[C/T]CTTTCCCCCAACACC	9079
rs157616	snp	A/T	0.326976	0.237854	intron-variant	LDB2	GRCh38.p7	4:16709344	TGCCTCAAGACCCAA[A/T]GGGAAACTCCATCTT	9079
rs157617	snp	G/T	0.495818	0.0455352	intron-variant	LDB2	GRCh38.p7	4:16710066	ACCAAGTTTGCCATA[G/T]ATAATGTGTCATATA	9079
rs157618	snp	A/G	0.495291	0.0482933	intron-variant	LDB2	GRCh38.p7	4:16710998	ATCTAAGGTATTCTT[A/G]GCTTTTTATGAAATT	9079
rs157619	snp	A/G	0.495252	0.0484902	intron-variant	LDB2	GRCh38.p7	4:16711452	TGAAGATGGGAAAAA[A/G]TGAGGATGATTGTGT	9079
rs157620	snp	G/T	0.483418	0.0895317	intron-variant	LDB2	GRCh38.p7	4:16701016	GTAAAATGGAGATAA[G/T]TAAAGTTCCTCTCTC	9079
rs157621	snp	A/C	0.328382	0.237395	intron-variant	LDB2	GRCh38.p7	4:16701136	AGATAATCTGAAGGG[A/C]AGGTGACATCTTAAG	9079
rs157622	snp	A/G	0.459233	0.136827	intron-variant	LDB2	GRCh38.p7	4:16701969	TACTTTACTGTGGCT[A/G]CTACTATTGCTATCA	9079
rs157623	snp	C/G	0.328616	0.237317	intron-variant	LDB2	GRCh38.p7	4:16702709	GTCTGCATGGGGATG[C/G]ATGAGTGAAGCTCAG	9079
rs157624	snp	C/T	0.458315	0.13822	intron-variant	LDB2	GRCh38.p7	4:16702887	CTTATAGCCCTTGAA[C/T]GCCTATGTACTCTCT	9079
rs157625	snp	C/T	0.4941	0.0539917	intron-variant	LDB2	GRCh38.p7	4:16702946	CCTCACCTGTACTTA[C/T]GCTGAATATCTAAGT	9079
rs157626	snp	A/G	0.494855	0.0504572	intron-variant	LDB2	GRCh38.p7	4:16702954	GTACTTACGCTGAAT[A/G]TCTAAGTTTAAATGT	9079
rs157627	snp	A/C	0.327211	0.237778	intron-variant	LDB2	GRCh38.p7	4:16704428	TTTATACTCCCCATA[A/C]CATCAAAAAATAATA	9079
rs157628	snp	A/G	0.457037	0.140127	intron-variant	LDB2	GRCh38.p7	4:16704823	ATCAATTGTAAGTGA[A/G]CAAGCAGTCTGTGGC	9079
rs157629	snp	C/T	0.325799	0.238232	intron-variant	LDB2	GRCh38.p7	4:16706598	GTTAAGTTATTTATG[C/T]GATAGTAGCAAACAC	9079
rs157630	snp	A/G	0.444533	0.157025	intron-variant	LDB2	GRCh38.p7	4:16751389	TCCATTATCTCATGC[A/G]ATCATTAGTGTGGTA	9079
rs157631	snp	G/T	0.375996	0.215928	intron-variant	LDB2	GRCh38.p7	4:16753265	CACCCAGCTATATTT[G/T]TACTGTGCTTGCTAT	9079
rs158260	snp	A/G	0.470811	0.117228	intron-variant	LDB2	GRCh38.p7	4:16837797	ACCACCATTTTATTT[A/G]TTTGTAGTACTGTGC	9079
rs158261	snp	C/T	0.488846	0.0738428	intron-variant	LDB2	GRCh38.p7	4:16839536	CCAAACTGGGtgtta[C/T]agtctgggtttgtat	9079
rs158262	snp	A/G	0.00557542	0.0525036	intron-variant	LDB2	GRCh38.p7	4:16829882	gaggccaaggcaagc[A/G]gatcacgaggtcaag	9079
rs158263	snp	A/G	0.478437	0.10157	intron-variant	LDB2	GRCh38.p7	4:16829918	gagaccatcctggcc[A/G]acatggtgaaaccct	9079
rs158264	snp	A/T	0.472429	0.114129	intron-variant	LDB2	GRCh38.p7	4:16832074	AATACCCAAAATAAC[A/T]GTTTTAAACAAATTA	9079
rs158265	snp	A/C	0.489665	0.0711382	intron-variant	LDB2	GRCh38.p7	4:16822215	ATATCTACTGTAAAA[A/C]TAATAGTTAATATTC	9079
rs158266	snp	C/T	0.466515	0.124985	intron-variant	LDB2	GRCh38.p7	4:16822818	gttaATATAAGAGCA[C/T]GTggtcgggcacggt	9079
rs158267	snp	A/C	0.462144	0.132269	intron-variant	LDB2	GRCh38.p7	4:16823676	TATTTATTTCTTTTT[A/C]TGTTTCAGTTCAAAG	9079
rs158268	snp	C/T	0.203882	0.245709	intron-variant	LDB2	GRCh38.p7	4:16824300	CAAGACTTCTAAGTC[C/T]AAAAGCTAGTGATAT	9079
rs158269	snp	A/T	0.479583	0.0989539	intron-variant	LDB2	GRCh38.p7	4:16825299	TGGCTATAATTTGTT[A/T]TTTCTGGTTAATCTC	9079
rs158270	snp	A/G	0.484066	0.0878235	intron-variant	LDB2	GRCh38.p7	4:16825963	ATGAATATACATGAC[A/G]TATTATACATACATA	9079
rs158271	snp	C/G	0.475702	0.107512	intron-variant	LDB2	GRCh38.p7	4:16826126	ATCTTTATCTCCTAT[C/G]TACATATTAGATAGA	9079
rs158272	snp	G/T	0.0766824	0.180169	intron-variant	LDB2	GRCh38.p7	4:16826290	ATTGGGACTAGAAGT[G/T]CTCTGAAGACTTTCA	9079
rs158273	snp	A/C	0.202651	0.245475	intron-variant	LDB2	GRCh38.p7	4:16851611	TTTCttttttttctt[A/C]ttatttttttttttt	9079
rs158274	snp	A/G	0.499928	0.00598999	intron-variant	LDB2	GRCh38.p7	4:16851768	TCTCTGTATGTCTTC[A/G]CTTCCTTCTCATTTG	9079
rs158275	snp	C/T	0.370772	0.218893	intron-variant	LDB2	GRCh38.p7	4:16852430	TCCTAGTTCATCCCA[C/T]GTGTGTGGAAGTTCA	9079
rs158276	snp	A/G	0.000798403	0.0199641	intron-variant	LDB2	GRCh38.p7	4:16806158	aagtcatggccatca[A/G]ttggtacctggaaga	9079
rs158277	snp	A/G	0.273318	0.24891	intron-variant	LDB2	GRCh38.p7	4:16797949	cttctggattcaagc[A/G]attctcctgcctcag	9079
rs158278	snp	A/G	0.422158	0.181278	intron-variant	LDB2	GRCh38.p7	4:16799418	GGAAACTGGGCATGG[A/G]GCTTATATCCCGTGA	9079
rs166867	snp	C/T	0	0	intron-variant	LDB2	GRCh38.p7	4:16628367	TCTCCTGGAGAAGTT[C/T]TAAGTCAAATGGCAA	9079
rs166879	snp	A/G	0.378372	0.214524	intron-variant	LDB2	GRCh38.p7	4:16725994	AAATATCCATTATAT[A/G]CTTATATATAATTTT	9079
rs166880	snp	C/T	0	0	intron-variant	LDB2	GRCh38.p7	4:16733476	TTCACAGGCCAGTTT[C/T]TAGGCTGTATTTGTG	9079
rs169501	snp	A/G			intron-variant	LDB2	GRCh38.p7	4:16715859	GGTGCTGCTGCTGTA[A/G]ACCTTTTTTATAATC	9079
rs169604	snp	A/G	0.478932	0.10045	intron-variant	LDB2	GRCh38.p7	4:16819403	ACCAAAATCTGACCT[A/G]AAGTACTGAATGTTT	9079
rs169605	snp	C/T	0.417845	0.185278	intron-variant	LDB2	GRCh38.p7	4:16811201	CAGATACCCTGAAGG[C/T]ACAGTGTGCAAAGCA	9079
rs169606	snp	C/T	0.438946	0.163706	intron-variant	LDB2	GRCh38.p7	4:16783065	gcctcaaattcttca[C/T]atctttgaagacatg	9079
rs172203	snp	A/G	0	0	intron-variant	LDB2	GRCh38.p7	4:16666594	GACATCCATGCAGTA[A/G]AAGCCTGGTGGAACC	9079
rs172210	snp	A/G			intron-variant	LDB2	GRCh38.p7	4:16734960	gcactttgggaggca[A/G]aggcgggtggatcac	9079
rs172211	snp	A/G	0	0	intron-variant	LDB2	GRCh38.p7	4:16752799	cctccataactgcca[A/G]atgttaggcatgtga	9079
rs176288	snp	G/T	0.0941369	0.195465	intron-variant	LDB2	GRCh38.p7	4:16785051	TATTATTTTTCTTTC[G/T]TTTACTATTATAAGC	9079
rs182232	snp	C/T	0	0	intron-variant	LDB2	GRCh38.p7	4:16688367	CAAGCCCTGCCTCCT[C/T]TGACATGAGGGCCTG	9079
rs183259	snp	A/G	0	0	intron-variant	LDB2	GRCh38.p7	4:16734600	GGCAGAGGAAGGGAA[A/G]AGGGTGCTTCAAAGG	9079
rs183998	snp	C/T	0	0	intron-variant	LDB2	GRCh38.p7	4:16734663	GCAGCTCTTCCTCAT[C/T]TTTGGTGAGAAATCA	9079
rs185830	snp	A/G			intron-variant	LDB2	GRCh38.p7	4:16757906	GCAGGTAGTATATCA[A/G]AAAATGGGCTGTTTA	9079
rs188170	snp	A/G	0	0	intron-variant	LDB2	GRCh38.p7	4:16686992	AAACATTAGGATGAA[A/G]AAAAAGGAGAGGTGG	9079
rs188179	snp	A/G	0	0	intron-variant	LDB2	GRCh38.p7	4:16753019	TCCACCTGAAACCTA[A/G]AAAGGCACAGGTTCC	9079
rs188263	snp	C/T	0	0	intron-variant	LDB2	GRCh38.p7	4:16844183	tcaggccttcacctt[C/T]taggcttacgcgatt	9079
rs189965	snp	A/G	0	0	intron-variant	LDB2	GRCh38.p7	4:16631901	ttattggtctattca[A/G]agattcaacttcttc	9079
rs189987	snp	A/G	0.155325	0.23138	intron-variant	LDB2	GRCh38.p7	4:16821295	AACAAAATAAAAATA[A/G]CACTCTTGATACCAA	9079
rs189988	snp	A/T	0.338296	0.233889	intron-variant	LDB2	GRCh38.p7	4:16768612	TGACCTGAGCTTCCT[A/T]CAGTGTGAGAGGGAC	9079
rs190747	snp	C/T			intron-variant	LDB2	GRCh38.p7	4:16628788	tgacaccccaccctt[C/T]ttcggctcaccctcc	9079
rs190754	snp	C/T	0	0	intron-variant	LDB2	GRCh38.p7	4:16757630	CCACCTTATTTTTTT[C/T]TGAGGCATAAGCTCA	9079
rs190755	snp	A/G	0	0	intron-variant	LDB2	GRCh38.p7	4:16710743	CCTAAACAATATTTA[A/G]ACTGAGCTTTATTGT	9079
rs192533	snp	A/G	0	0	intron-variant	LDB2	GRCh38.p7	4:16739115	TTGGGGGGCGCCTTA[A/G]ATTGGTTTAATTAAA	9079
rs204939	snp	G/T	0	0	intron-variant	LDB2	GRCh38.p7	4:16739337	ggcctcccaaagcgg[G/T]gggattacagtcatg	9079
rs204976	snp	A/C	0	0	intron-variant	LDB2	GRCh38.p7	4:16713101	aaagaagccagaaac[A/C]caatatgatttcatt	9079
rs207677	snp	C/T	0.0766824	0.180169	intron-variant	LDB2	GRCh38.p7	4:16820572	CAGGAAAGCTCTGCC[C/T]GGTATGGGGCTGACT	9079
rs207678	snp	A/G	0.485049	0.0851591	intron-variant	LDB2	GRCh38.p7	4:16819095	CACACACACACACAC[A/G]CAAGCAACCACAACT	9079
rs207679	snp	A/T	0.246485	0.249975	intron-variant	LDB2	GRCh38.p7	4:16818746	AAAAATATATACAAC[A/T]TCCTTCTTGGAGCTG	9079
rs207680	snp	A/G	0.0755793	0.179102	intron-variant	LDB2	GRCh38.p7	4:16817438	CTTAAAAGAGATAAA[A/G]AATTGTAAACAAAGG	9079
rs207681	snp	G/T	0.448323	0.15221	intron-variant	LDB2	GRCh38.p7	4:16768782	TGAGTTCAGAAGGGT[G/T]ACTGGCATACAATAA	9079
rs207682	snp	A/G	0.330714	0.236612	intron-variant	LDB2	GRCh38.p7	4:16769386	TCGCTTGAACCCAAG[A/G]GGCGGAGGTTGCAGT	9079
rs207683	snp	C/T	0.364609	0.222182	intron-variant	LDB2	GRCh38.p7	4:16770682	GAGTAGAGATTGCAA[C/T]AGGCAGCGAGTAAAG	9079
rs207684	snp	C/T	0.407502	0.194147	intron-variant	LDB2	GRCh38.p7	4:16771596	gagaaactggaatta[C/T]attatggagatggaa	9079
rs207685	snp	A/G	0.356597	0.226135	intron-variant	LDB2	GRCh38.p7	4:16771700	atgtgttggaggtaa[A/G]ttcatgggatttgct	9079
rs207686	snp	C/G	0.448195	0.152377	intron-variant	LDB2	GRCh38.p7	4:16772435	GGGAGATTAATGTGT[C/G]TCCTTGATAGATTTA	9079
rs207687	snp	A/G	0.448195	0.152377	intron-variant	LDB2	GRCh38.p7	4:16773207	aggttggggacTGAC[A/G]GCTTATAGCATTTTC	9079
rs207688	snp	A/G	0.334412	0.235318	intron-variant	LDB2	GRCh38.p7	4:16814678	TCTAGCATAGCAGCT[A/G]GCAATTGAAAAGCTC	9079
rs207689	snp	G/T	0.417359	0.185718	intron-variant	LDB2	GRCh38.p7	4:16812409	AAACAAGCAACCGTA[G/T]GTTAAAACTTTAACT	9079

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