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
rs4108	snp	G/T	0.412416	0.190055	intron-variant	CORO2B	GRCh38.p7	15:68659230	tatccctcacactct[G/T]ccaggtttaaGTATG	10391
rs593719	snp	A/G	0.41408	0.188621	intron-variant	CORO2B	GRCh38.p7	15:68568509	TTTGTAGCTGAGGAC[A/G]CTGGGACCCCAAAAG	10391
rs596373	snp	C/G	0.413582	0.189052	intron-variant	CORO2B	GRCh38.p7	15:68570983	TTTTTGATGATGGCA[C/G]AAAGCACTTAATCAG	10391
rs597284	snp	C/T	0.322721	0.23919	intron-variant	CORO2B	GRCh38.p7	15:68582231	GAGAACTTCTAGCCC[C/T]GTGGCATTTCTCCTG	10391
rs615188	snp	C/G	0.132751	0.2208	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577243	TAGGAATGGACCCTG[C/G]AGTTCACGGATTCAA	10391
rs622851	snp	A/G	0.397994	0.201489	intron-variant	CORO2B	GRCh38.p7	15:68570334	AGTTGTTTAGAGCTT[A/G]CACCATCTATCTGCA	10391
rs625937	snp	A/C	0.385315	0.212113	intron-variant	CORO2B	GRCh38.p7	15:68564448	agctgggactacagg[A/C]gcgtgccactacaac	10391
rs625961	snp	A/G	0.372794	0.217765	intron-variant	CORO2B	GRCh38.p7	15:68571032	GAAAGTGCGAAGGAA[A/G]CAGAGAGGAGGGAAT	10391
rs626797	snp	A/G	0.474634	0.109726	intron-variant	CORO2B	GRCh38.p7	15:68564659	AGTTTGTATCTTAGC[A/G]GATTCAAAATTATCA	10391
rs628703	snp	G/T	0.331874	0.236213	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577976	CTTGCCAGGCTGTCC[G/T]GCTTGGAGAACCCCT	10391
rs644791	snp	C/T	0.418974	0.184249	intron-variant	CORO2B	GRCh38.p7	15:68566933	ACCTGAGCTTGCCAG[C/T]GAAGAGGCAGCGTGT	10391
rs656209	snp	A/G	0.383824	0.211166	intron-variant	CORO2B	GRCh38.p7	15:68565237	TTAATATATTGATAT[A/G]TTTTCTCCTGTTTTG	10391
rs656812	snp	A/G	0.307919	0.243198	intron-variant	CORO2B	GRCh38.p7	15:68590997	TTTGCTGAGCCCTGT[A/G]TGCCAGGCCCTAAGC	10391
rs674038	snp	A/G	0.381891	0.212379	intron-variant	CORO2B	GRCh38.p7	15:68566945	CAGCGAAGAGGCAGC[A/G]TGTCCAATAAATGAC	10391
rs687209	snp	A/G	0.413748	0.188909	intron-variant	CORO2B	GRCh38.p7	15:68567576	ctcccagaggaatgt[A/G]tagggcttgctgcct	10391
rs688109	snp	C/T	0.0205511	0.0992634	intron-variant	CORO2B	GRCh38.p7	15:68569711	ttttgtaagaaattg[C/T]cacagggtcttccaa	10391
rs694686	snp	C/T	0.400504	0.199621	intron-variant	CORO2B	GRCh38.p7	15:68576286	CCTTGCTTTTCTAGA[C/T]CTCCCTTCTGCCTGG	10391
rs728400	snp	A/G	0.274393	0.248807	intron-variant	CORO2B	GRCh38.p7	15:68593035	GGTGAGGGTCATCCC[A/G]TGGCAGAGGCATCAC	10391
rs728401	snp	A/G	0.42574	0.177808	intron-variant	CORO2B	GRCh38.p7	15:68593475	TAGCAGCCAGGTCTG[A/G]ATGTAGCCCTACTCC	10391
rs728402	snp	G/T	0.274393	0.248807	intron-variant	CORO2B	GRCh38.p7	15:68593007	GAAGTCCAAGAGCAT[G/T]GCACCAGCATCTGGT	10391
rs746118	snp	C/T	0.414905	0.187899	intron-variant	CORO2B	GRCh38.p7	15:68676481	AAGGATAACCACCGC[C/T]GCCTAAACCCGTCAA	10391
rs749555	snp	A/G	0.254664	0.249956	intron-variant	CORO2B	GRCh38.p7	15:68667675	GGCTGAGAAGGGGGA[A/G]GTAGTGAATAGAGAG	10391
rs755135	snp	A/G/T	0	0	intron-variant	CORO2B	GRCh38.p7	15:68604080	TTGTGAGCACTGAGT[A/G/T]TATTTCATACACAGA	10391
rs764204	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68593177	atgacttaatcccct[C/T]ttaaaggccccatct	10391
rs893843	snp	G/T	0.0696718	0.173152	intron-variant	CORO2B	GRCh38.p7	15:68667879	GGGCTTCGGGACCTG[G/T]AGTCCTGACCCAGCC	10391
rs893844	snp	C/G	0.449853	0.150196	intron-variant	CORO2B	GRCh38.p7	15:68637374	CCTCCTGTGTGTCCA[C/G]CTTTCCCGGGTGGAG	10391
rs893845	snp	C/G	0.447421	0.153379	intron-variant	CORO2B	GRCh38.p7	15:68637764	CCACATTACACAGCT[C/G]TTTCCCAGGGGGCTT	10391
rs920920	snp	A/G	0	0	intron-variant	CORO2B	GRCh38.p7	15:68566680	CAAATAAGGCTCCAT[A/G]AGCCTGACTTCCCTT	10391
rs930432	snp	C/T	0.0629771	0.165899	intron-variant	CORO2B	GRCh38.p7	15:68658412	ACCCCCACTGGCCCC[C/T]CACTGGCCGAAGGCA	10391
rs930433	snp	C/T	0.468949	0.12067	intron-variant	CORO2B	GRCh38.p7	15:68658368	GATGGCAGGCGGGGA[C/T]GAGGCCCCCAGCCAG	10391
rs937095	snp	A/G	0.496416	0.0421803	intron-variant	CORO2B	GRCh38.p7	15:68633776	TACTACAACGGAGCC[A/G]GCAGATCGTCCTTCT	10391
rs937096	snp	C/G	0.497804	0.0611406	intron-variant	CORO2B	GRCh38.p7	15:68633784	CGGAGCCGGCAGATC[C/G]TCCTTCTCTTCCATG	10391
rs937097	snp	A/G	0.0637235	0.166737	intron-variant	CORO2B	GRCh38.p7	15:68707409	AAGAATATCCACACC[A/G]CTGCACAAACTTGGA	10391
rs937098	snp	A/G	0.338069	0.233974	intron-variant	CORO2B	GRCh38.p7	15:68602220	GAATAAAGCCAGTCA[A/G]CAGTTCCCCCCACTC	10391
rs937099	snp	A/C	0.174932	0.238463	intron-variant	CORO2B	GRCh38.p7	15:68698808	GAGATGAGCAGGCAT[A/C]GATGAAGGGACAGGC	10391
rs937100	snp	A/G	0.258565	0.249853	intron-variant	CORO2B	GRCh38.p7	15:68720383	gttacacagcagtag[A/G]tagctaatacaGGTG	10391
rs937101	snp	A/G	0.388398	0.208197	intron-variant	CORO2B	GRCh38.p7	15:68720168	CATGCAGCCATCTCC[A/G]TTTCAGTTGTATCAG	10391
rs937102	snp	G/T	0.0372196	0.131242	intron-variant	CORO2B	GRCh38.p7	15:68710556	GTCTCAGGGTGTGGC[G/T]GGAGAGGAAGGAGAC	10391
rs937103	snp	C/T	0.441021	0.161279	intron-variant	CORO2B	GRCh38.p7	15:68689370	TGTACAATGACTGTT[C/T]AGATGGTCGGCTCAC	10391
rs995971	snp	C/G	0.330714	0.236612	intron-variant	CORO2B	GRCh38.p7	15:68674395	GTCTGTAACTCGGGA[C/G]TGAAGCCAGCGAATG	10391
rs1106285	snp	C/G	0.478104	0.102316	intron-variant	CORO2B	GRCh38.p7	15:68677780	CCATTCTGTGTGTCT[C/G]CTGCCTCCCCTCTCC	10391
rs1123931	snp	C/T	0.273856	0.248859	intron-variant	CORO2B	GRCh38.p7	15:68626982	AGGAGTCTTGCTACA[C/T]ATCCTGTGCTCAGAG	10391
rs1128848	snp	C/G	0.497241	0.037038	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727243	CACATAGGATCTCAT[C/G]GAGCCTCACGTCTAC	10391
rs1128869	snp	C/T			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727701	CCTCCTCCCACATTT[C/T]TGGAGCTTTTTTTTT	10391
rs1317998	snp	C/G	0.322245	0.239334	intron-variant	CORO2B	GRCh38.p7	15:68603680	CTGTGCAGATGCGGA[C/G]AGAGTGAGCTCTCTG	10391
rs1352833	snp	C/T	0.332337	0.236052	intron-variant	CORO2B	GRCh38.p7	15:68717986	AGTCCTTTGGCAAGT[C/T]ACAACTCTCTGAGCT	10391
rs1352834	snp	C/T	0.202959	0.245534	intron-variant	CORO2B	GRCh38.p7	15:68717909	AGGTGATCAGCAGAA[C/T]ATGTTCCAAGATACT	10391
rs1352835	snp	C/T	0.331411	0.236373	intron-variant	CORO2B	GRCh38.p7	15:68717766	CACATAAAGGAATTC[C/T]AGGAGCTGGAGGTAA	10391
rs1352836	snp	A/G	0.234401	0.249513	intron-variant	CORO2B	GRCh38.p7	15:68713308	GTTGGGGGCTACACC[A/G]CTTCAGGAGCTCTCA	10391
rs1388444	snp	C/T	0.132409	0.220618	intron-variant	CORO2B	GRCh38.p7	15:68682089	AAGCTGAAGCAGGGG[C/T]TCCTCCTACCCAGGG	10391
rs1388445	snp	C/G	0.473818	0.111381	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630871	TTACATCCTCAAATG[C/G]AAGCAAAGGCGGGAA	10391
rs1388446	snp	A/C	0.331179	0.236453	intron-variant	CORO2B	GRCh38.p7	15:68718165	ACCAACAATGTGTGC[A/C]CATGTTTCCTGTGTG	10391
rs1388447	snp	A/G	0.232651	0.249397	intron-variant	CORO2B	GRCh38.p7	15:68688920	GAGGAGGGCATGGAC[A/G]CCCTGCTCCAGGATG	10391
rs1388448	snp	C/T	0.232651	0.249397	intron-variant	CORO2B	GRCh38.p7	15:68688798	ATTCTGCTTCAGGAA[C/T]TTACCCCAGGGAAAT	10391
rs1463700	snp	C/T	0.347473	0.230215	intron-variant	CORO2B	GRCh38.p7	15:68716676	gctcaacttaaaata[C/T]catcatcacagagag	10391
rs1463701	snp	A/G	0.276267	0.248616	intron-variant	CORO2B	GRCh38.p7	15:68716372	aggtgccttgcacat[A/G]tggtctctaagcctt	10391
rs1463702	snp	A/G	0.19646	0.2442	intron-variant	CORO2B	GRCh38.p7	15:68711243	CCTTTTTTTGAGGAT[A/G]TGCCTGGGGCTCGGG	10391
rs1463703	snp	G/T	0.463774	0.129618	intron-variant	CORO2B	GRCh38.p7	15:68710216	CCCCAGGTCTCTCCT[G/T]AGAGATGGTGGACTT	10391
rs1465997	snp	A/G	0.482905	0.0908579	intron-variant	CORO2B	GRCh38.p7	15:68589185	GAGTTCCTGTAGCAT[A/G]TGATCCCTGGTATAC	10391
rs1467976	snp	G/T	0.0755793	0.179102	intron-variant	CORO2B	GRCh38.p7	15:68649619	ttatatctgtcaata[G/T]ttagcatattcaaaa	10391
rs1491632	snp	C/T	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68611550	GCTTTCAGTTGAAGA[C/T]ATATCCAAACAGAGA	10391
rs1491633	snp	C/T	0.36021	0.224397	intron-variant	CORO2B	GRCh38.p7	15:68664803	aaaaggaaatgcaaa[C/T]agattgtaagcatac	10391
rs1491634	snp	A/G	0.172997	0.237846	intron-variant	CORO2B	GRCh38.p7	15:68662857	CATTTACTGGCATAA[A/G]ATATATACAAATCTA	10391
rs1491635	snp	C/T	0.298905	0.24517	intron-variant	CORO2B	GRCh38.p7	15:68658842	CATCAGGCCTCCATG[C/T]TGCATTCTGATCAGC	10391
rs1491636	snp	A/G	0.449473	0.150701	intron-variant	CORO2B	GRCh38.p7	15:68638254	TCAAATGTTTACTTG[A/G]GGAGGTCAGGCTTTG	10391
rs1491637	snp	C/T	0.258843	0.249844	intron-variant	CORO2B	GRCh38.p7	15:68722432	TCACACTTAGATCAA[C/T]GCGTCCACCTTTGAC	10391
rs1491638	snp	C/T	0.25912	0.249834	intron-variant	CORO2B	GRCh38.p7	15:68722380	GCTTCCGAACTGCTA[C/T]GATGATTAAAACTGT	10391
rs1491639	snp	A/G	0.301429	0.244653	intron-variant	CORO2B	GRCh38.p7	15:68719055	TCTTACTGATCTCCA[A/G]TCACTCTACCTGCTC	10391
rs1491640	snp	G/T	0.475753	0.244715	intron-variant	CORO2B	GRCh38.p7	15:68719050	CTGATCTCCAGTCAC[G/T]CTACCTGCTCTCCTG	10391
rs1491641	snp	C/T	0.312104	0.242163	intron-variant	CORO2B	GRCh38.p7	15:68718916	TTTGAAGACCCCAGT[C/T]CACAGCACATCTCTC	10391
rs1542746	snp	A/C	0.085535	0.188285	intron-variant	CORO2B	GRCh38.p7	15:68715317	GGCAGCCTCGGGGCC[A/C]CTTACCTAGGCCTTT	10391
rs1542747	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68624752	ggctggagtgcaatg[G/T]catgatctcggctca	10391
rs1562158	snp	C/T	0.250168	0.25	intron-variant	CORO2B	GRCh38.p7	15:68558093	CAGGGAGGGTGGGTG[C/T]GGGCAGAGAGGCTTC	10391
rs1562159	snp	A/G	0.494013	0.0543839	intron-variant	CORO2B	GRCh38.p7	15:68561093	CACCCCGCGTCCCCC[A/G]GGCTCCCAGCACAAC	10391
rs1562160	snp	A/G	0.383824	0.211166	intron-variant	CORO2B	GRCh38.p7	15:68561112	TCCCAGCACAACTTT[A/G]CCTCTCAATACTGGT	10391
rs1562162	snp	C/G	0	0	intron-variant	CORO2B	GRCh38.p7	15:68591218	ACGTGGCTGGGCAGG[C/G]CAAGGAAGCTCTCTG	10391
rs1562163	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68591219	CGTGGCTGGGCAGGC[C/G]AAGGAAGCTCTCTGG	10391
rs1562164	snp	A/G	0	0	intron-variant	CORO2B	GRCh38.p7	15:68591220	GTGGCTGGGCAGGCC[A/G]AGGAAGCTCTCTGGA	10391
rs1565563	snp	A/G	0.180064	0.240019	intron-variant	CORO2B	GRCh38.p7	15:68593244	GGCTACGGTTTGAAT[A/G]TCTCTGCCAAAACTC	10391
rs1565564	snp	A/G	0.347694	0.230122	intron-variant	CORO2B	GRCh38.p7	15:68716891	CTAATGCATCCCATG[A/G]ATTTAGCCCCTGCCC	10391
rs1602544	snp	A/T	0.388964	0.20782	intron-variant	CORO2B	GRCh38.p7	15:68662979	gcctagaaatatttt[A/T]aaaaatttaagaaaa	10391
rs1602545	snp	A/G	0.0685596	0.171987	intron-variant	CORO2B	GRCh38.p7	15:68662769	catttgcagttgaga[A/G]aaatgtaaacaaatg	10391
rs1866685	snp	A/G	0.330947	0.236533	intron-variant	CORO2B	GRCh38.p7	15:68638321	GAGAGGGTAGAGCTA[A/G]TGTTGAGCAAGCACC	10391
rs1866686	snp	A/G	0.0337553	0.125452	intron-variant	CORO2B	GRCh38.p7	15:68641865	agtagctgagactat[A/G]ggtgtgtaccactat	10391
rs1873573	snp	A/G	0.463343	0.130326	intron-variant	CORO2B	GRCh38.p7	15:68707677	TAAAAAGAAAGAAGT[A/G]TGTGTGTCTATATGT	10391
rs1907565	snp	A/G	0.466308	0.125343	intron-variant	CORO2B	GRCh38.p7	15:68655226	AACCTGGATCTTTTA[A/G]TAATAGAAGAAATAT	10391
rs1966275	snp	A/G	0.0970103	0.197722	intron-variant	CORO2B	GRCh38.p7	15:68650079	GAAGAAATGCAATAT[A/G]CGATTAATCACATTA	10391
rs1968979	snp	C/T	0	0	intron-variant	CORO2B	GRCh38.p7	15:68596067	CTGCACAACTCCCAC[C/T]TCCCCGCAAGCCACC	10391
rs1975513	snp	C/T	0.187685	0.242109	intron-variant	CORO2B	GRCh38.p7	15:68558403	gacagggtctcgctt[C/T]gttaaccaggctgga	10391
rs1985277	snp	C/T	0.289424	0.246872	intron-variant	CORO2B	GRCh38.p7	15:68558174	AGTTGACAGGTGAGG[C/T]TGGTGTTCTGACCCG	10391
rs1994714	snp	C/T	0.403158	0.197592	intron-variant	CORO2B	GRCh38.p7	15:68585096	CTGGGAGCCTCCCAT[C/T]GCTACATTAATTAAT	10391
rs1994715	snp	C/T	0.404035	0.196909	intron-variant	CORO2B	GRCh38.p7	15:68584977	GTGGCTTCTCCCCCA[C/T]TCCCCACCCCCACCC	10391
rs1994716	snp	A/G	0.439363	0.163222	intron-variant	CORO2B	GRCh38.p7	15:68691757	AACAGAGAGGAGCCT[A/G]TTTAGAAGAAGGAGT	10391
rs2004092	snp	A/G	0.416871	0.186156	intron-variant	CORO2B	GRCh38.p7	15:68675650	TACAAAAATAGATCT[A/G]TAAACATCTTATTTG	10391
rs2017617	snp	A/G	0.495483	0.0473088	intron-variant	CORO2B	GRCh38.p7	15:68560723	GGGAGCACAGCTGGA[A/G]AGCGGCCCTGACCAG	10391
rs2044342	snp	A/T	0.406814	0.194704	intron-variant	CORO2B	GRCh38.p7	15:68560321	ttcttctgagacagg[A/T]tctcgctctgtcacc	10391
rs2046923	snp	C/G	0.4711	0.116682	intron-variant	CORO2B	GRCh38.p7	15:68654511	AGATCAAGCAGACTG[C/G]CAGATGCTTCAGAGG	10391
rs2046924	snp	A/G	0.0622301	0.165053	intron-variant	CORO2B	GRCh38.p7	15:68654258	CCAAATCCAGAGAAC[A/G]CCCATCCCATAACCT	10391
rs2046925	snp	A/G	0.464735	0.128019	intron-variant	CORO2B	GRCh38.p7	15:68654124	CAAGCTGTCAATCTC[A/G]AGCCTCAGACAAATG	10391
rs2087707	snp	C/T	0.47852	0.101384	intron-variant	CORO2B	GRCh38.p7	15:68678433	GCCCAAGTCGGCCTC[C/T]CAAAGTGTTGGGATT	10391

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