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
rs10638	snp	A/G	0.488241	0.0757703	utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033955	CATAACTGGACTGAA[A/G]ATTTAACGTAAGGCT	55884
rs13649	snp	A/G	0	0	utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033658	ATACCAAATGGCTCC[A/G]GGAAAACTGTCCTGC	55884
rs4128857	snp	A/G	0.318656	0.240388	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118063760	AATAAGTGCCAACTG[A/G]TATTTCTCACGTTGG	55884
rs4128858	snp	C/T	0.456803	0.140473	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118063793	ATCATCCTTACTAGG[C/T]AAAATGTATTATGAT	55884
rs4131122	snp	C/G	0.329084	0.237162	intron-variant	WSB2	GRCh38.p7	12:118059383	AGACTTCTGTTGGTC[C/G]GGGCTGGCCTAGAGG	55884
rs4767655	snp	A/C	0.356169	0.226336	intron-variant	WSB2	GRCh38.p7	12:118055717	CCTCCTGGGTTCAAG[A/C]AATTCTTATGCCTCA	55884
rs4767656	snp	C/T	0.460813	0.134379	intron-variant	WSB2	GRCh38.p7	12:118057313	agagtctcactctgc[C/T]gcccaggctggagtg	55884
rs5745897	snp	A/G	0.00199481	0.0315187	downstream-variant-500B, utr-variant-3-prime, intron-variant	RFC5, WSB2	GRCh38.p7	12:118032318	CCCCTTAAGGACAGC[A/G]GCAAAGTATGAAGCT	55884
rs5745898	snp	G/T	0.0360663	0.129354	downstream-variant-500B, utr-variant-3-prime, intron-variant	RFC5, WSB2	GRCh38.p7	12:118032333	GGCAAAGTATGAAGC[G/T]AAATATCTGATGGCC	55884
rs5745899	snp	C/T	0.0154538	0.0865337	downstream-variant-500B, utr-variant-3-prime, intron-variant	RFC5, WSB2	GRCh38.p7	12:118032386	AGGCTCAGCATCTGC[C/T]GTACCTGGAACTTCA	55884
rs5745900	snp	C/T	0.00795532	0.062565	downstream-variant-500B, utr-variant-3-prime	RFC5, WSB2	GRCh38.p7	12:118032491	ttttttgaggcaaga[C/T]catgctctgtcagtc	55884
rs5801265	in-del	-/A	0.325799	0.238232	intron-variant	WSB2	GRCh38.p7	12:118053601	GCACACCATCTTGTG[-/A]AAGAGTAGGCACCAG	55884
rs6144890	in-del	-/ACATT	0.488905	0.0736498	intron-variant	WSB2	GRCh38.p7	12:118059220	AAAAAAAAATCTAAA[-/ACATT]ACATTACAATTTATT	55884
rs7134751	snp	C/T	0.369142	0.219784	intron-variant	WSB2	GRCh38.p7	12:118057350	cgccatctcggctca[C/T]tgcaacctccgcccc	55884
rs7135150	snp	C/G	0.00318978	0.0398085	intron-variant	WSB2	GRCh38.p7	12:118049801	CAGCATGCAGAGTAC[C/G]CATCTCAACAAACTC	55884
rs7136393	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118052683	ACTCCTCACTGCTGG[G/T]TAACCATGACTCACA	55884
rs7300357	snp	C/T	0.0520825	0.152737	intron-variant	WSB2	GRCh38.p7	12:118055062	ATATTTTTATATATA[C/T]GGTCTGAGTAAATAG	55884
rs7300973	snp	A/T			intron-variant	WSB2	GRCh38.p7	12:118048289	CTCAGAATACTGTTC[A/T]TCAAAATATGTGATT	55884
rs7306158	snp	A/G	0.0663309	0.169604	intron-variant	WSB2	GRCh38.p7	12:118050085	catgcctgtaatccc[A/G]gctactcaggaggct	55884
rs7310726	snp	G/T	0.143959	0.226396	intron-variant	WSB2	GRCh38.p7	12:118054841	AAGCCTTTGTAAAGA[G/T]ACTATTCATTCTCAG	55884
rs7312586	snp	A/G	0.425277	0.178263	intron-variant	WSB2	GRCh38.p7	12:118043069	TGAGTGGGGCAGGGA[A/G]GCGACATAGTCAGAA	55884
rs7484385	snp	G/T			intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061377	AAGACGCGCGAACCA[G/T]ATAAAAATGGGGCAG	55884
rs7484410	snp	C/G/T			intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061446	ACGGGATAAAACCCA[C/G/T]GGGTTGTGCGGGGTC	55884
rs7485457	snp	A/C	0.0722614	0.17581	intron-variant	WSB2	GRCh38.p7	12:118056076	CTGCTCTCCCGGCTT[A/C]CCCTCTAGCCCCGCA	55884
rs7485548	snp	A/G	0.198324	0.244601	intron-variant	WSB2	GRCh38.p7	12:118051201	acagacaataacaac[A/G]gctggatgtagagaa	55884
rs7486055	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118055047	AAAAAAGAAAGAAAT[A/C]TATTTTTATATATAT	55884
rs7487673	snp	A/G	0	0	intron-variant	WSB2	GRCh38.p7	12:118054000	agtatttttttctca[A/G]ttatacatgatgata	55884
rs7488835	snp	A/C	0.270351	0.24917	intron-variant	WSB2	GRCh38.p7	12:118051376	acatgaaaacaaccc[A/C]atgtccatcaactga	55884
rs7963217	snp	C/G/T	0.0659589	0.169201	intron-variant	WSB2	GRCh38.p7	12:118051749	gaggccgaggtgggt[C/G/T]aatcacttgaggtca	55884
rs7967764	snp	A/G	0.49975	0.0111793	intron-variant	WSB2	GRCh38.p7	12:118043729	TGGGATTACTGGCAT[A/G]AGCCACCCCACCCGG	55884
rs9788041	snp	C/T	0.433675	0.169598	synonymous-codon	WSB2	GRCh38.p7	12:118035249	AAGGTACAAGCCTTC[C/T]GGAGAGAAGCACACA	55884
rs9888438	snp	A/G	0.00398564	0.0444627	intron-variant	WSB2	GRCh38.p7	12:118054747	TAGGAAAATAATAAC[A/G]TAGGTATATCTTGTT	55884
rs10558297	in-del	-/TATT			downstream-variant-500B, utr-variant-3-prime, intron-variant	RFC5, WSB2	GRCh38.p7	12:118032697	CTAAGTTTTTTTGGC[-/TATT]TATTTATTTATTTTT	55884
rs10624358	in-del	-/TC			intron-variant	WSB2	GRCh38.p7	12:118034583	AAAGCGCTCTCTCTG[-/TC]TCTCTCTCTCGGCAC	55884
rs10774977	snp	A/G	0.489142	0.0728777	intron-variant	WSB2	GRCh38.p7	12:118058993	GAGCCACCCCGGCGC[A/G]TTTGGTTGATATTTT	55884
rs10850952	snp	G/T	0.482008	0.0931261	intron-variant	WSB2	GRCh38.p7	12:118040273	GTGGGGCAGCGCCTG[G/T]CAGCTGGGAACCAAC	55884
rs11068778	snp	A/T	0.5	0	intron-variant	WSB2	GRCh38.p7	12:118037668	AGCGAAACTCTGTCT[A/T]AAAAAAAAAAAAAAG	55884
rs11068779	snp	C/T	0.284471	0.247612	intron-variant	WSB2	GRCh38.p7	12:118038162	TGCAGGTGGTGGCCA[C/T]GGCCCACCAGCATGC	55884
rs11068780	snp	C/T	0.29341	0.246202	intron-variant	WSB2	GRCh38.p7	12:118038274	GAATTAAAGCAATAA[C/T]GCTGGAGACTCACCG	55884
rs11068781	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118039790	gttctgttgcctagg[C/T]gggagtgcaatggca	55884
rs11068782	snp	A/G	0.0887219	0.191022	intron-variant	WSB2	GRCh38.p7	12:118040487	CACTGCCagccgagc[A/G]tggtacctcatacct	55884
rs11068783	snp	A/G	0.0603597	0.1629	intron-variant	WSB2	GRCh38.p7	12:118041937	tttttgtatttttta[A/G]tagagatggggtttg	55884
rs11068784	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118045117	TGCGGTGGCTCATGC[C/T]TGTAATCCCAGCACT	55884
rs11068785	snp	A/T			intron-variant	WSB2	GRCh38.p7	12:118045118	GCGGTGGCTCATGCT[A/T]GTAATCCCAGCACTT	55884
rs11068786	snp	C/G			intron-variant	WSB2	GRCh38.p7	12:118045141	CAGCACTTTGGGAGG[C/G]CAAGGTGGGCAGATC	55884
rs11068787	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118046879	agggctcgagcagtc[C/T]ttccatctcagcctc	55884
rs11068788	snp	A/G	0.347253	0.230308	intron-variant	WSB2	GRCh38.p7	12:118047635	GGAGGATCACTTGAG[A/G]CAAGGAGTTCAAGGC	55884
rs11068790	snp	C/T	0.35574	0.226537	intron-variant	WSB2	GRCh38.p7	12:118054339	gaggttacagtgagc[C/T]gagatcgtgccactg	55884
rs11068791	snp	A/T	0.330714	0.236612	intron-variant	WSB2	GRCh38.p7	12:118054684	CTCTGTCTCAAAAAA[A/T]AATAATAATAATAAT	55884
rs11068792	snp	C/T	0.316968	0.240864	intron-variant	WSB2	GRCh38.p7	12:118054825	GTTAATAAATCATAT[C/T]AAGCCTTTGTAAAGA	55884
rs11068793	snp	A/C	0.0614824	0.164198	intron-variant	WSB2	GRCh38.p7	12:118057080	TAAAAGAAGAACAAA[A/C]CCAGTGACTCCTGTC	55884
rs11068794	snp	A/G	0.339203	0.233544	intron-variant	WSB2	GRCh38.p7	12:118057495	GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG	55884
rs11068795	snp	A/C	0.48955	0.071525	intron-variant	WSB2	GRCh38.p7	12:118057938	tttttttttttttaa[A/C]ttaaatttttagtag	55884
rs11068796	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118058368	TTTTATTTTTTTTGA[A/G]ACAGGGTCTTGCTCT	55884
rs11068797	snp	C/T	0.378372	0.214524	intron-variant	WSB2	GRCh38.p7	12:118058416	GCAGTAGCACCATCA[C/T]GGCTCACTGCAACCT	55884
rs11068798	snp	A/G	0.489083	0.0730708	intron-variant	WSB2	GRCh38.p7	12:118058494	GCTGGGACTACAGGC[A/G]CATTCTACCATGCAC	55884
rs11068799	snp	G/T	0.316968	0.240864	intron-variant	WSB2	GRCh38.p7	12:118059685	GATTGCTTTCAGATT[G/T]AACTGTAAGGAGGCA	55884
rs11308776	in-del	-/T	0	0	intron-variant	WSB2	GRCh38.p7	12:118055924	CTGTTTTTTTTTTTT[-/T]AAATCTCCCAAACCA	55884
rs11426565	in-del	-/A			intron-variant	WSB2	GRCh38.p7	12:118055016	AAAAAAAAAAAAAAA[-/A]GAAAAAAGAAAGAAA	55884
rs11540133	snp	G/T			utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033244	GCTGTTTAACTTCAT[G/T]GGATTAATCAGCTGG	55884
rs11540134	snp	G/T			utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033309	AATTGTGTAAAGAAT[G/T]GGTGTAGTCATGACT	55884
rs11540135	snp	C/T			utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033198	GAAACAAAAATAGCT[C/T]CTTAAAAGTACTGTT	55884
rs11550988	snp	A/T			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118063773	TACCAGTTGGCACTT[A/T]TTGCATCATAATACA	55884
rs11613209	snp	A/C	0.019353	0.0964467	intron-variant	WSB2	GRCh38.p7	12:118054216	GTCTCTACTAAAAAT[A/C]CAAAAAAAAAAAAAA	55884
rs11832085	snp	C/G			intron-variant	WSB2	GRCh38.p7	12:118051589	agacaaagtagatta[C/G]tggttgcctggagag	55884
rs12228444	snp	A/G	0.000905611	0.0212599	synonymous-codon	WSB2	GRCh38.p7	12:118034246	TCTTGGGGATTGGCA[A/G]TGCTAGGACTTGGTA	55884
rs12229137	snp	C/T	0.161924	0.233971	intron-variant	WSB2	GRCh38.p7	12:118046355	ATAGTCCCAGCTACT[C/T]GGGAGGCTGAAGCAG	55884
rs12300828	snp	C/T	0.00199481	0.0315187	intron-variant	WSB2	GRCh38.p7	12:118039143	AGACTGTCACCCTCC[C/T]AGCCTTGCCAGGATG	55884
rs12302795	snp	C/G	0.423257	0.180228	intron-variant	WSB2	GRCh38.p7	12:118040438	ATGGTGGCAAGCTGC[C/G]TCAGTACACACATTA	55884
rs12309202	snp	C/T	0.0944967	0.195752	intron-variant	WSB2	GRCh38.p7	12:118039293	CTCCAGCTCTTGCTT[C/T]AAAAATAAAAAAGCC	55884
rs12310685	snp	A/G	0.488424	0.0751925	intron-variant	WSB2	GRCh38.p7	12:118044115	CGAAGGCAAAACTCT[A/G]TCTCAAAAAAAAAAA	55884
rs12311489	snp	C/T	0.00396038	0.0443227	intron-variant	WSB2	GRCh38.p7	12:118048261	TCAATAAGCCTCATA[C/T]TGCAAACATTTCCTC	55884
rs12313999	snp	G/T	0.279195	0.248289	intron-variant	WSB2	GRCh38.p7	12:118039377	AGTTGGAATTAGAGA[G/T]AGATTTTCCATGGGG	55884
rs12319850	snp	C/T	0.00835141	0.0640778	intron-variant	WSB2	GRCh38.p7	12:118034826	GAGAAAATGGGACAC[C/T]GTTATTAGCAAAATC	55884
rs12320789	snp	G/T	0	0	intron-variant	WSB2	GRCh38.p7	12:118046396	tgagcccaggaggca[G/T]aggttgcagtgaacc	55884
rs12578639	snp	A/T	0.299411	0.245069	intron-variant	WSB2	GRCh38.p7	12:118051831	ATACAAAACTTAGCC[A/T]GGCGTGGTGGTGTGT	55884
rs12579444	snp	C/T	0.28052	0.24813	intron-variant	WSB2	GRCh38.p7	12:118058731	gatggagtttcactc[C/T]tgttgcccaggctgg	55884
rs12582265	snp	A/G	0.195837	0.244062	intron-variant	WSB2	GRCh38.p7	12:118044547	AACTGATGGTAACCC[A/G]CACAAGGATCAAACA	55884
rs12582327	snp	C/T	0.0023933	0.0345097	intron-variant	WSB2	GRCh38.p7	12:118051639	ctaaattaaggggta[C/T]agggtttctttctga	55884
rs12818975	snp	G/T			intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061313	TCGGGGAGGCGGTAC[G/T]CTGACGGGATAAAAG	55884
rs12819129	snp	G/T			intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061392	GATAAAAATGGGGCA[G/T]GGGTGGGGGGAGCTG	55884
rs12823138	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118049115	TCATATAGTAAATTT[A/G]CTTACATGTCAAGTC	55884
rs12828248	snp	A/T			intron-variant	WSB2	GRCh38.p7	12:118049113	ATTCATATAGTAAAT[A/T]TACTTACATGTCAAG	55884
rs12830847	snp	G/T	0.320814	0.239761	intron-variant	WSB2	GRCh38.p7	12:118039980	CGAACTCCTGACCTC[G/T]AGTGATCCGCCCGCC	55884
rs12833894	snp	A/C	0.33303	0.235809	upstream-variant-2KB	WSB2	GRCh38.p7	12:118062721	GGTTACACTCCTGTT[A/C]ACCCCGCTTGGCCGG	55884
rs16948110	snp	G/T	0.1128	0.208988	utr-variant-3-prime, intron-variant	WSB2, RFC5	GRCh38.p7	12:118032917	CAAAAGCTTTTAACT[G/T]TTGTTTTTTTCTTTT	55884
rs33933604	in-del	-/TC			intron-variant	WSB2	GRCh38.p7	12:118034584	TCTSTSTCTCTCTCT[-/TC]CGGCACAGCCCTTTC	55884
rs34253698	snp	A/G	0.00848367	0.0645745	synonymous-codon	WSB2	GRCh38.p7	12:118036433	AGAGTCGGGGGAGAA[A/G]TCACAAGAGACAACA	55884
rs34549466	snp	C/T	0.000527209	0.0162273	missense	WSB2	GRCh38.p7	12:118035290	AGCTAATGTGGACGT[C/T]ACTGTCATCCATGGC	55884
rs34606067	snp	C/T	0.375	0.216506	intron-variant	WSB2	GRCh38.p7	12:118043026	GGGCACGAGGTGTGC[C/T]TGCCACGGCCACACC	55884
rs34646347	in-del	-/G			intron-variant	WSB2	GRCh38.p7	12:118043477	GAGTGGAGGGAAGGG[-/G]TCTGTCACCCAAGCT	55884
rs34818152	in-del	-/G			downstream-variant-500B, utr-variant-3-prime, intron-variant	RFC5, WSB2	GRCh38.p7	12:118032373	TCAAACCACCCAGAG[-/G]CTCAGCATCTGCTGT	55884
rs34947187	in-del	-/T			intron-variant	WSB2	GRCh38.p7	12:118045001	TACCACCATTACTTT[-/T]GCACCAACCCAATAT	55884
rs35299550	in-del	-/A/AA/AG			utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033564	AAAAAAAAAAAAAAA[-/A/AA/AG]GCCAGTAATAGTGTC	55884
rs35369829	in-del	-/C			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118063668	AATTTCTCCCAACCT[-/C]CCCCCCACCACATCT	55884
rs35426707	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118053933	TTACATTTTGACCTC[A/G]CTGAAATCAGGATGT	55884
rs35499134	in-del	-/TTT			downstream-variant-500B, cds-indel, intron-variant	RFC5, WSB2	GRCh38.p7	12:118032714	TTTATTTATTTATTT[-/TTT]AAATAAAGATTGGGT	55884
rs35749330	in-del	-/A			intron-variant	WSB2	GRCh38.p7	12:118047124	CTACTTTATTCCAAA[-/A]GAATTAAGGCATATT	55884
rs36027266	in-del	-/T			upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063428	GTGATGGAGGCTCCG[-/T]TCTGGAGGAAAAAAA	55884
rs55816764	snp	A/G	0.0941369	0.195465	intron-variant	WSB2	GRCh38.p7	12:118050771	CTGAAAAGATGCTCG[A/G]CCAGGTGTGGTGGCT	55884

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