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
rs6678	snp	A/G	0.355609	0.226598	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:890165	CTCCAGGCAGGTGAT[A/G]GCCTCGTGGTGCTCT	10025
rs11492	snp	A/C	0.0112582	0.074178	synonymous-codon	MED16	GRCh38.p7	19:886088	CAGGGACACGGTGAC[A/C]AGGCCGCTGACCGTC	10025
rs13090	snp	A/G	0.382621	0.211936	missense	MED16	GRCh38.p7	19:868115	GACCATCTGCATCCA[A/G]AGGACCGTCCGTGAC	10025
rs891206	snp	C/T	0.493201	0.0579089	intron-variant	MED16	GRCh38.p7	19:872255	TCGGTGCCAGAAGCA[C/T]CCCAGTCCTGACCAC	10025
rs1060442	snp	C/T	0.4794	0.0993767	synonymous-codon	MED16	GRCh38.p7	19:885818	CCGCAAGGACAAGTT[C/T]CCCGCCATCACCCAC	10025
rs1616408	snp	C/T	0.498568	0.0267188	intron-variant	MED16	GRCh38.p7	19:877516	GGTCAGTGGGGTGGC[C/T]CACAGCACGTATTAG	10025
rs1617214	snp	C/G	0.338069	0.233974	intron-variant	MED16	GRCh38.p7	19:877437	ACTCCTCAGGTAAAG[C/G]AGACGAGTGTAAGCC	10025
rs1631848	snp	A/G	0.39544	0.20334	intron-variant	MED16	GRCh38.p7	19:868551	AAGTGGGGCAGGCGT[A/G]AGGGAGGCCCGCCTG	10025
rs1651881	snp	A/G	0	0	intron-variant	MED16	GRCh38.p7	19:878805	GAGCTGCTGGGGCAC[A/G]TGGGGCTGGGGCTGG	10025
rs1651882	snp	A/G	0.321292	0.23962	intron-variant	MED16	GRCh38.p7	19:878721	TGGTGGGGATTGACA[A/G]CCAGGGGAAGGCGAG	10025
rs1651883	snp	C/T			intron-variant	MED16	GRCh38.p7	19:879287	ACAACCATGGGAAGG[C/T]GAGCTGCTGGGCATT	10025
rs1651884	snp	C/T			intron-variant	MED16	GRCh38.p7	19:879199	ACAACCATGGGAAGG[C/T]GAGCTGCTGGGCATT	10025
rs1651885	snp	G/T			intron-variant	MED16	GRCh38.p7	19:879123	TGGGGCTGGGGCTGG[G/T]GGGTATTGACAACCA	10025
rs1651886	snp	A/G	0.350764	0.228794	intron-variant	MED16	GRCh38.p7	19:876641	CAGGTAGCCTGTGGC[A/G]GGTGAGGCTGCGTGT	10025
rs1651887	snp	C/T	0.298651	0.24522	intron-variant	MED16	GRCh38.p7	19:875902	CTCTCCAACTCCCAG[C/T]CTCCAGGAATCCTCC	10025
rs1651888	snp	C/T	0.368529	0.220116	intron-variant	MED16	GRCh38.p7	19:873743	CTCCCAGTTCCTCTC[C/T]GTCCGGCAACGCCAT	10025
rs1651889	snp	C/G	0.488118	0.0761554	intron-variant	MED16	GRCh38.p7	19:873341	TCAGCCCCGCCCCTA[C/G]TTGGAGTCCCGCCCC	10025
rs1651890	snp	C/G	0.393987	0.204372	intron-variant	MED16	GRCh38.p7	19:870946	CACGGCTCCCTCCCT[C/G]CATGTCCTGCCCCAG	10025
rs1651891	snp	C/T	0.279991	0.248195	intron-variant	MED16	GRCh38.p7	19:868620	TGTGGCAGGTGGGGA[C/T]GTGGGGAGCAGGCGT	10025
rs1683565	snp	C/T	0.368119	0.220336	intron-variant	MED16	GRCh38.p7	19:880602	GGACTCCTTTCATAT[C/T]CTCTTTTCCATGAGC	10025
rs1683566	snp	C/T	0.367091	0.220884	intron-variant	MED16	GRCh38.p7	19:880560	GACCCCACCTCCCCC[C/T]GGCCCTCGTACAATG	10025
rs1683567	snp	G/T			intron-variant	MED16	GRCh38.p7	19:879175	GGGCATTGACAACCA[G/T]GGGAAGGCGAGCTgc	10025
rs1683568	snp	A/C	0.0209421	0.100162	intron-variant	MED16	GRCh38.p7	19:879047	gTGGGCATTGACAAC[A/C]GGGGGAAGGTGAGCT	10025
rs1683569	snp	A/G	0.402052	0.198444	synonymous-codon	MED16	GRCh38.p7	19:871135	GGGCTGCAGGCGGCT[A/G]ACCAGGCCGTCGCTG	10025
rs1683570	snp	A/G	0.434543	0.168653	intron-variant	MED16	GRCh38.p7	19:871447	GCTGGGTGACCCCAG[A/G]GTTCTCTCCCCGTCT	10025
rs1683573	snp	A/G	0.500538	0.0133903	intron-variant	MED16	GRCh38.p7	19:872614	CCGGGTGGGTGGGGC[A/G]GAAGAAATCACAGCT	10025
rs1683574	snp	A/G	0.458272	0.138286	intron-variant	MED16	GRCh38.p7	19:872877	CGGGGCTTTGAGAAT[A/G]GGCAGGAAGGGTGTG	10025
rs1683575	snp	C/G	0.434976	0.168179	intron-variant	MED16	GRCh38.p7	19:873258	GGGGTGGGACTCCAA[C/G]CAGGGGCGGGGCTGA	10025
rs1683576	snp	C/G	0.0573587	0.15934	intron-variant	MED16	GRCh38.p7	19:873962	CTGCAGCCACCCCCG[C/G]CTGGCAGCTGGCGGC	10025
rs1683588	snp	C/T	0.262985	0.249663	intron-variant	MED16	GRCh38.p7	19:870489	actgcaacgtctgcc[C/T]ctcgggttcaaatga	10025
rs1683589	snp	A/G	0	0	intron-variant	MED16	GRCh38.p7	19:869564	GGGGCCTCCTAATGA[A/G]TCACACACGAGGGTT	10025
rs1683590	snp	C/T	0.388775	0.207946	intron-variant	MED16	GRCh38.p7	19:869496	GTTACGTCAGAGGCT[C/T]GTAAACTGGGAAAAT	10025
rs1683591	snp	C/T	0.38934	0.207568	intron-variant	MED16	GRCh38.p7	19:869037	TGTGAGGCCGGCCAT[C/T]CCCTCCACCCCCGCC	10025
rs1683592	snp	C/T	0.258843	0.249844	downstream-variant-500B	MED16	GRCh38.p7	19:867774	GTGGATGGGATGGGG[C/T]GGCCATCGTCAGGGT	10025
rs1683593	snp	C/T	0.369142	0.219784	downstream-variant-500B	MED16	GRCh38.p7	19:867735	TCCAGGCATCTGCCT[C/T]TCAGTGTGTTGTCTG	10025
rs2241623	snp	A/G	0.424193	0.179323	intron-variant	MED16	GRCh38.p7	19:876604	TGCTCCCAGAGGCCC[A/G]TCCAGGAAAGCTGCA	10025
rs2288546	snp	A/G	0.144969	0.226867	intron-variant	MED16	GRCh38.p7	19:871457	GACAGGCCAGAGACG[A/G]GGAGAGAACTCTGGG	10025
rs2303820	snp	A/G	0.0146672	0.084371	intron-variant	MED16	GRCh38.p7	19:869061	CATCTGGGCCCACCT[A/G]GCAGATGGTGTGAGG	10025
rs2365702	snp	A/G	0.406296	0.19512	intron-variant	MED16	GRCh38.p7	19:881413	CCCATCAGAACCCAG[A/G]AGGCTGAGCTCCTAC	10025
rs2365703	snp	A/G	0.439502	0.163061	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892615	CTCCAGACCCCTATA[A/G]CTCCGCAGTCCCCAG	10025
rs2365704	snp	A/C	0.5	0	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892888	GAGCCCCGAGCCCCG[A/C]GCCCCGCGCCCCGCG	10025
rs2365705	snp	A/C	0.5	0	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892895	gagccccgagccccg[A/C]gccccgcgccccgcg	10025
rs2629995	snp	C/G	0.5	0	intron-variant	MED16	GRCh38.p7	19:879480	GTGGGGCTGGGGCTG[C/G]TGGGCATTGACAACC	10025
rs2629996	snp	A/G	0.346368	0.23068	intron-variant	MED16	GRCh38.p7	19:878598	GGCGTTGACAACCAC[A/G]GGAAGGTGAGCTGCT	10025
rs2930891	snp	C/T	0.370974	0.218781	intron-variant	MED16	GRCh38.p7	19:883224	ATGCCAGGCTTCGGT[C/T]CCTACCATGCCCAGC	10025
rs2930892	snp	C/T	0.482831	0.0910472	intron-variant	MED16	GRCh38.p7	19:882943	CCACTGTGTGCCCTC[C/T]GGGCGTCTCAGCCAC	10025
rs2930893	snp	C/G	0.319616	0.240112	intron-variant	MED16	GRCh38.p7	19:882724	GCCAGCAGCCCTGCA[C/G]TGTTTCTGTTTCTGT	10025
rs2930894	snp	C/T	0.367091	0.220884	intron-variant	MED16	GRCh38.p7	19:881161	CACACTCTTCAGTGC[C/T]TACCCTATTTGCTCA	10025
rs2930895	snp	C/T	0.450985	0.148678	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893080	GGCCGACCAGGTGAG[C/T]GCGGGGCTGCGGGGG	10025
rs2930896	snp	C/G	0.48	0.0979796	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:891740	AGGTGTTCCCTGTCA[C/G]TCAGCCCCGCCTCGG	10025
rs2930898	snp	C/T	0.374	0.217081	intron-variant	MED16	GRCh38.p7	19:883968	GGGAAGGAATGGCAG[C/T]GGCCCTCTTCACCTT	10025
rs2930899	snp	C/G	0.402806	0.197864	intron-variant	MED16	GRCh38.p7	19:885398	GGGCCGCCTCTCACA[C/G]AGAAGGGACCTGCGG	10025
rs2930900	snp	A/G	0.255224	0.249945	intron-variant	MED16	GRCh38.p7	19:886257	CATGGGGGCTGCCCC[A/G]TGACCCCCAGAAACA	10025
rs2930901	snp	A/G	0.344815	0.231323	intron-variant	MED16	GRCh38.p7	19:886945	ttagccgggcatggt[A/G]gcgggtgcctataat	10025
rs2930902	snp	A/G	0.141687	0.225598	intron-variant	MED16	GRCh38.p7	19:887128	TCTACGTTGTGAAAA[A/G]ATGCGAGGAAGAGAA	10025
rs2930903	snp	C/G	0.499776	0.0105807	intron-variant	MED16	GRCh38.p7	19:887824	ggacaggcagatcca[C/G]agagacaactgggtc	10025
rs2930904	snp	A/G	0.0271762	0.113356	intron-variant	MED16	GRCh38.p7	19:888161	gtgagccgagatcgc[A/G]ccactacactccagc	10025
rs2930905	snp	C/T	0.270351	0.24917	intron-variant	MED16	GRCh38.p7	19:888663	GGTCTGTGAACTCCA[C/T]CCCGACAAAACTGTT	10025
rs2965290	snp	A/G	0.401747	0.198678	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892003	CAGGTGTTCCCCGTC[A/G]CACTCAGCCCCGCCT	10025
rs2965291	snp	C/G/T	0.266273	0.24947	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:891948	CTCAGCCCCCGGCTC[C/G/T]GCCACAGGTGTTCCC	10025
rs2965292	snp	C/T	0.348354	0.22984	intron-variant	MED16	GRCh38.p7	19:890844	ACCTCTCACTCACCC[C/T]GGCCCTCCTCTGTAA	10025
rs2965293	snp	A/G	0.344147	0.231595	intron-variant	MED16	GRCh38.p7	19:888384	GGCACCCACCACCAC[A/G]CCTGGCTAATTTTTG	10025
rs2965294	snp	C/G	0.493748	0.0555599	intron-variant	MED16	GRCh38.p7	19:884782	CGGCCCTAAGCGATC[C/G]TCTCGCCTCGATCTC	10025
rs3111332	snp	C/T			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892886	ctgagccccgagccc[C/T]gagccccgagccccg	10025
rs3217342	in-del	-/TCCTCAGCTAC	0.000404904	0.0142228	intron-variant	MED16	GRCh38.p7	19:868340	CTACTCCTCAGCTAC[-/TCCTCAGCTAC]CCCTCAGCTGCCCCT	10025
rs4417648	snp	A/G	0.37138	0.218556	intron-variant	MED16	GRCh38.p7	19:883725	GACACAGACGTGCCC[A/G]GCGGGGGCACCGGGC	10025
rs4806813	snp	A/G	0.40086	0.199352	intron-variant	MED16	GRCh38.p7	19:881094	CAGGGAAGAACGGGA[A/G]CTGGGGGAAGAAAGG	10025
rs4807142	snp	C/T	0.404384	0.196635	intron-variant	MED16	GRCh38.p7	19:874960	TTGAGGTCAAGAGTT[C/T]GAGACCAGCCTGGCC	10025
rs4807153	snp	A/G	0.404035	0.196909	intron-variant	MED16	GRCh38.p7	19:881049	CCCTGAGCCCCGAGC[A/G]GGTTTTGATAAATGC	10025
rs7253106	snp	G/T	0.0314385	0.121371	intron-variant	MED16	GRCh38.p7	19:885468	TGGGGGGGGTCCGGG[G/T]GCCCCAGTGTCCTCA	10025
rs7253460	snp	C/G	0.402982	0.197728	intron-variant	MED16	GRCh38.p7	19:885706	GGTCTCCACCCCCAG[C/G]ACCCTGAGAAGCAGT	10025
rs7256798	snp	A/G	0.0283406	0.115616	intron-variant	MED16	GRCh38.p7	19:870213	GGGGCCAGAGACTAA[A/G]GGCAGAGGCTAAGGC	10025
rs7257260	snp	A/G	0.0142736	0.0832652	intron-variant	MED16	GRCh38.p7	19:870592	aaaaaaaGGGAGAGG[A/G]TGAATGGAAGGGCTG	10025
rs8100009	snp	A/G	0.0176367	0.0922351	synonymous-codon	MED16	GRCh38.p7	19:871048	GCACCTGGCGAGGCC[A/G]TCGAGCTGCAGGGTG	10025
rs8100258	snp	A/G	0.370503	0.219041	synonymous-codon	MED16	GRCh38.p7	19:871222	ATCCACCAGCGCCTC[A/G]TCCGGCTCGCTCGCT	10025
rs8105744	snp	A/G	0.343477	0.231866	downstream-variant-500B	MED16	GRCh38.p7	19:867595	TGGAGAAACATAACA[A/G]GGACAGAGTCAGGCA	10025
rs9676834	snp	A/G			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:891613	ACAGGGAACACCTGT[A/G]GCCGAGGCGGGGCTG	10025
rs10401425	snp	C/G			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892682	CGCACCGATAACCCC[C/G]CAGTCTCCAGGCCCT	10025
rs10412830	snp	C/T			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892688	GATAACCCCGCAGTC[C/T]CCAGGCCCTGCCTCT	10025
rs10414386	snp	A/G			intron-variant	MED16	GRCh38.p7	19:876911	GGCCCCACCTGCCAC[A/G]GGGCCCCCACCTGCC	10025
rs10415140	snp	C/G	0.467234	0.12373	upstream-variant-2KB	MED16	GRCh38.p7	19:894169	gcctcccgagtagct[C/G]ggactacaggcgcgc	10025
rs10415271	snp	A/C/T	0.5	0	intron-variant	MED16	GRCh38.p7	19:870222	GACTAAGGGCAGAGG[A/C/T]TAAGGCAGGGCGCCC	10025
rs10415544	snp	C/T			intron-variant	MED16	GRCh38.p7	19:870392	attgcaaaaccgcct[C/T]tataccaaaaataca	10025
rs10422235	snp	C/G	0.479824	0.098392	upstream-variant-2KB	MED16	GRCh38.p7	19:895062	ctgcactccagcctg[C/G]gggacagagcaagac	10025
rs10424998	snp	C/G	0.243061	0.249904	intron-variant	MED16	GRCh38.p7	19:874647	CAGGAGTAGAGAgag[C/G]tgaaaggatcgcttg	10025
rs10425005	snp	A/G	0.276534	0.248588	intron-variant	MED16	GRCh38.p7	19:874658	Agaggtgaaaggatc[A/G]cttgagctcaggtgg	10025
rs10425219	snp	C/G	0.0209421	0.100162	intron-variant	MED16	GRCh38.p7	19:874779	tccagaggctgaggc[C/G]agattgcttgagccc	10025
rs10451478	snp	C/G	0.0644693	0.167566	intron-variant	MED16	GRCh38.p7	19:883883	TGGGGACCGGGCGAA[C/G]GAACGAGCCCTGGGA	10025
rs11085228	snp	A/G	0.0741063	0.177655	intron-variant	MED16	GRCh38.p7	19:883464	GGCATGGCGGGGACC[A/G]AAGCCTGGCATGGTG	10025
rs11546307	snp	C/T	0.329837	0.236909	synonymous-codon	MED16	GRCh38.p7	19:875389	GCCCTGCACGGTGAC[C/T]CGCGTGTGCGACTAC	10025
rs11878213	snp	C/T	0.497271	0.0368399	upstream-variant-2KB	MED16	GRCh38.p7	19:894722	aggacagcttgagtt[C/T]gagaccagcctggga	10025
rs11878467	snp	C/T	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:889982	CACCCTGAACAAGAA[C/T]GATTCGGGCCACTAT	10025
rs11878621	snp	C/T	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:890073	GACTGACCGGAGAAA[C/T]ACAGGGCCCCCCTGC	10025
rs11879638	snp	C/G	0.479904	0.0982045	upstream-variant-2KB	MED16	GRCh38.p7	19:894790	aaattagcagggttg[C/G]ggagggaggggcgct	10025
rs11879857	snp	A/G	0.0494327	0.149241	intron-variant	MED16	GRCh38.p7	19:882481	gtgagccaagatcac[A/G]ccactgcactccagc	10025
rs11879886	snp	A/G	0.0144652	0.0838055	intron-variant	MED16	GRCh38.p7	19:889821	GCCTGAGGGCAAGAA[A/G]CCATCATTGCGAACC	10025
rs11879913	snp	A/G	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:889918	AGAGGTCTCGGCCCA[A/G]GTAGGGCACAGCAGG	10025
rs11883077	snp	A/G	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:889898	GGGGGAAGCCAGCCC[A/G]GTGGAGAGGTCTCGG	10025
rs12460696	snp	A/G	0.393065	0.205018	intron-variant	MED16	GRCh38.p7	19:870453	GTAATCCCAGCTACT[A/G]GGAAGGCTGAGGTAG	10025
rs12461907	snp	G/T			intron-variant	MED16	GRCh38.p7	19:872586	GAAGGGCGGGCCCCA[G/T]GGCAGGATGAAGCCG	10025

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