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
rs697234	snp	C/T	0.154661	0.231107	intron-variant	PPARG	GRCh38.p7	3:12459698	AAAAAAGAACAGAAT[C/T]TGAGAACCAGTGACC	5468
rs709147	snp	C/T	0.388775	0.207946	intron-variant	PPARG	GRCh38.p7	3:12407441	GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC	5468
rs709148	snp	G/T	0.495056	0.049474	intron-variant	PPARG	GRCh38.p7	3:12408667	CTGAGGTGGGAGGAC[G/T]GCTTGAGCCCCGAGT	5468
rs709149	snp	C/T	0.390277	0.206936	intron-variant	PPARG	GRCh38.p7	3:12408855	TAAGTTCTTGACCAC[C/T]GAGGCTTTTTTTTTA	5468
rs709150	snp	C/G	0.495016	0.0496707	intron-variant	PPARG	GRCh38.p7	3:12409838	ATGCTGAGCGGGCAG[C/G]GCGCATTCTACAATA	5468
rs709151	snp	A/G	0.36606	0.221428	intron-variant	PPARG	GRCh38.p7	3:12413500	TTTTCAATCCTTTCT[A/G]CATTCTGAAGAAGAG	5468
rs709152	snp	C/T	0.46974	0.119223	intron-variant	PPARG	GRCh38.p7	3:12413535	AGGCATGAGCCACCA[C/T]GCCCGGCCCCATTCC	5468
rs709153	snp	C/T	0.36606	0.221428	intron-variant	PPARG	GRCh38.p7	3:12413681	AGGCACCCACCACCA[C/T]GCCCGGCAATTTTTT	5468
rs709154	snp	A/T	0.365024	0.221967	intron-variant	PPARG	GRCh38.p7	3:12415335	CTGTGGTGAGCCATG[A/T]GACTTAAGAAAAGTC	5468
rs709155	snp	A/T	0.365646	0.221644	intron-variant	PPARG	GRCh38.p7	3:12415944	CAGGTTTAAAAAAAT[A/T]TTTTTTTCTTAAAAT	5468
rs709156	snp	A/G	0.27008	0.249192	intron-variant	PPARG	GRCh38.p7	3:12420116	TACACATATGTGTAC[A/G]TTCATAGCAGTTTGT	5468
rs709157	snp	A/G	0.195837	0.244062	intron-variant	PPARG	GRCh38.p7	3:12420525	AGTTGGCCTCATTCT[A/G]AGCTGGCTGTGGATT	5468
rs709158	snp	A/G	0.367503	0.220665	intron-variant	PPARG	GRCh38.p7	3:12421677	GAGGAAATTCACTGG[A/G]TTTTACAATATATTT	5468
rs709159	snp	A/C	0.41275	0.189769	intron-variant	PPARG	GRCh38.p7	3:12439704	CACTCCTAATTTTAG[A/C]CTAATATTACATAGT	5468
rs709166	snp	C/T	0.497613	0.0344622	intron-variant	PPARG	GRCh38.p7	3:12470153	GAGAGCTTGCACTTG[C/T]GGGCATTTGTGTGAC	5468
rs709167	snp	A/C	0.499527	0.0153681	intron-variant	PPARG	GRCh38.p7	3:12461456	GCTCCTGAAGTTTCC[A/C]AAACAAAAAGGAAAT	5468
rs796289	snp	C/T	0.0111196	0.0737302	intron-variant	PPARG	GRCh38.p7	3:12419869	AGCATACTATATATC[C/T]CATGTCTATTCTTTT	5468
rs796290	snp	C/G	0.470715	0.117409	intron-variant	PPARG	GRCh38.p7	3:12408184	GAAAGTTTTCTCAGA[C/G]CGAAGCTTTCTTAGT	5468
rs796313	snp	A/C	0.470618	0.117591	intron-variant	PPARG	GRCh38.p7	3:12408029	TCCCAGGTCTTCTAC[A/C]CACTTGCTGTGGGGT	5468
rs880663	snp	C/T	0.38934	0.207568	intron-variant	PPARG	GRCh38.p7	3:12328584	TATTGGTCTGGCTGG[C/T]GTGCCTAGTGGAAAG	5468
rs895095	snp	A/T	0.289165	0.246913	intron-variant	PPARG	GRCh38.p7	3:12396175	CGCCCAGTCTGGAGT[A/T]CAATGGTACAATCTT	5468
rs895096	snp	A/C	0.289165	0.246913	intron-variant	PPARG	GRCh38.p7	3:12396176	GCCCAGTCTGGAGTA[A/C]AATGGTACAATCTTG	5468
rs963702	snp	C/T	0	0	intron-variant	PPARG	GRCh38.p7	3:12447405	TGTGCCCATAGCATC[C/T]CATACTAAGTTCCGT	5468
rs963703	snp	C/T			intron-variant	PPARG	GRCh38.p7	3:12447241	TCTTTTTCTTTCTCT[C/T]TCTTTCTTTCTCCTT	5468
rs964232	snp	C/T	0.0410537	0.137264	intron-variant	PPARG	GRCh38.p7	3:12371738	GCCAAGCTGGGCTCC[C/T]GTCCAGTCAGCCTCT	5468
rs1064061	snp	G/T	0	0	intron-variant	PPARG	GRCh38.p7	3:12328109	AAGGTGTAGGAAGAA[G/T]GTTTATTCTTCAGTC	5468
rs1064323	snp	A/G	0.220843	0.248294	intron-variant	PPARG	GRCh38.p7	3:12360508	ttattgaagtataat[A/G]tacttagaggaaaaa	5468
rs1122648	snp	C/T	0.41141	0.19091	intron-variant	PPARG	GRCh38.p7	3:12333892	CAGGCCCCCATCTTC[C/T]GTGAAGCCATTGTCC	5468
rs1151987	snp	C/T	0.49655	0.04139	intron-variant	PPARG	GRCh38.p7	3:12463424	AACACGGTGAAACCC[C/T]GTCTCTATTAAAAAA	5468
rs1151988	snp	A/G	0.497473	0.0354532	intron-variant	PPARG	GRCh38.p7	3:12470013	GCAAGAGTAGCTGGC[A/G]TTATTGAGCACCCGC	5468
rs1151996	snp	G/T	0.38555	0.210062	intron-variant	PPARG	GRCh38.p7	3:12404308	ATACAACTATTGTTT[G/T]GTAGGGGCCTCCTTA	5468
rs1151997	snp	C/T	0.494976	0.0498674	intron-variant	PPARG	GRCh38.p7	3:12404505	GAGATAGTTATTTTA[C/T]ATGTTATTATGCTAA	5468
rs1151998	snp	C/T	0.495016	0.0496707	intron-variant	PPARG	GRCh38.p7	3:12404993	GTCCACTGTTCCCCA[C/T]GCATACATAGCTCTG	5468
rs1151999	snp	A/C	0.494896	0.0502606	intron-variant	PPARG	GRCh38.p7	3:12405654	AAAAGTTAATGCATA[A/C]TCCTGCTGAGAAAGT	5468
rs1152000	snp	A/G	0	0	intron-variant	PPARG	GRCh38.p7	3:12406396	TTATTTTGATGCCGA[A/G]AAAGGAGATGGATCC	5468
rs1152001	snp	C/T	0.291493	0.246533	intron-variant	PPARG	GRCh38.p7	3:12430363	TAGACCGTGAGGTAT[C/T]AGAGGGCAGAGACTA	5468
rs1152002	snp	A/G	0.475348	0.108251	intron-variant	PPARG	GRCh38.p7	3:12430372	CTCCCCCGTTAGACC[A/G]TGAGGTATCAGAGGG	5468
rs1152003	snp	C/G	0.499218	0.0197529	intron-variant	PPARG	GRCh38.p7	3:12435556	TCTCTTTTCTGAACT[C/G]AGAGGCTAACTATCC	5468
rs1152004	snp	A/G	0.287085	0.247234	intron-variant	PPARG	GRCh38.p7	3:12441605	GGAAAGGATAGTGAA[A/G]CATGCCAAGGCCGGC	5468
rs1152005	snp	C/T	0.296873	0.245566	intron-variant	PPARG	GRCh38.p7	3:12441952	GGGGCAAGGAGAATA[C/T]TCCGCACAGGTGGAC	5468
rs1152006	snp	C/T	0.453087	0.145793	intron-variant	PPARG	GRCh38.p7	3:12445548	CCAGCCTCAAAGCCA[C/T]AGGAAGTCCCCTCTC	5468
rs1152007	snp	C/G	0.453209	0.145623	intron-variant	PPARG	GRCh38.p7	3:12446048	tctagccacagaagt[C/G]tgctttgctgttcca	5468
rs1152008	snp	G/T	0.469544	0.119585	intron-variant	PPARG	GRCh38.p7	3:12446113	ccccaggagtgctct[G/T]gactgaggactgatg	5468
rs1175377	snp	A/G	0.0236746	0.106192	intron-variant	PPARG	GRCh38.p7	3:12449877	TACCCAAGGACACGT[A/G]GTTTTTAAATTGGCA	5468
rs1175378	snp	C/T	0.497151	0.037632	intron-variant	PPARG	GRCh38.p7	3:12469852	GCCTGGACGACAGTG[C/T]GAGACTCCATCTCAA	5468
rs1175381	snp	C/T	0.0248432	0.108648	intron-variant	PPARG	GRCh38.p7	3:12444345	GAACTCCCAGTTCTG[C/T]CACTTAATGgcctca	5468
rs1175540	snp	A/C	0.48491	0.0855403	intron-variant	PPARG	GRCh38.p7	3:12423744	CAGCTAAATATTTAC[A/C]TCCCTCATCCGTAGA	5468
rs1175541	snp	A/C	0.363985	0.222503	intron-variant	PPARG	GRCh38.p7	3:12423989	CTATGTTGTTTCTGC[A/C]TAGCTTCTGAGGCTC	5468
rs1175542	snp	A/G	0.495483	0.0473088	intron-variant	PPARG	GRCh38.p7	3:12424715	GGAGGGCTCACCAGC[A/G]TCACAAGTAGGTAGA	5468
rs1175543	snp	A/G	0.36955	0.219562	intron-variant	PPARG	GRCh38.p7	3:12424934	CATGTTCAGCACACA[A/G]TAAATGCTAATTTTC	5468
rs1175544	snp	C/T	0.351853	0.228311	intron-variant	PPARG	GRCh38.p7	3:12425545	GGTAGAGCCACCAGA[C/T]GGATTCAGGGCATGG	5468
rs1175545	snp	A/G	0.0134861	0.0810011	intron-variant	PPARG	GRCh38.p7	3:12441686	AAGAAAAGGTGGCAC[A/G]ACCTCCAGAGGGCTG	5468
rs1177809	snp	A/G	0.367297	0.220775	intron-variant	PPARG	GRCh38.p7	3:12424991	AAGCAGCGCCACTCA[A/G]TCCTGCCAGTCACAT	5468
rs1181795	snp	C/T	0.081446	0.184634	intron-variant	PPARG	GRCh38.p7	3:12443693	ctcttatctgtatga[C/T]ggtcacagcctcctc	5468
rs1184332	snp	C/T	0.35574	0.226537	intron-variant	PPARG	GRCh38.p7	3:12444922	TCATCTAATCCTCCA[C/T]ATGGCCCTGTTAGGT	5468
rs1185783	snp	A/G	0.110872	0.20771	intron-variant	PPARG	GRCh38.p7	3:12449487	GGAAGGCTCCAGTGA[A/G]CTGTGTTTGTACCAC	5468
rs1185784	snp	C/T	0.147656	0.228091	intron-variant	PPARG	GRCh38.p7	3:12452779	ATGAGGAAATTAAGG[C/T]TCAGCGAAGAGAAGT	5468
rs1185785	snp	A/G	0	0	intron-variant	PPARG	GRCh38.p7	3:12406451	TCGGGTTCTTCCCAG[A/G]GGAAAGCAAGGCTGC	5468
rs1186464	snp	A/G	0.155656	0.231515	intron-variant	PPARG	GRCh38.p7	3:12446012	ctcaggcaAGGAACC[A/G]CAGGGGCTGGCGGCC	5468
rs1373640	snp	C/T	0.281049	0.248064	intron-variant	PPARG	GRCh38.p7	3:12361102	ataccaacacaccca[C/T]cagaatggctaacgt	5468
rs1373641	snp	A/G	0.320096	0.239972	intron-variant	PPARG	GRCh38.p7	3:12360975	agaactgttggcaac[A/G]tctcctgaagctcaa	5468
rs1373642	snp	G/T	0.210909	0.246925	intron-variant	PPARG	GRCh38.p7	3:12408152	TATTATGTCTCCCTG[G/T]CTTACTACCAGCAAG	5468
rs1596667	snp	A/C	0.402454	0.198136	intron-variant	PPARG	GRCh38.p7	3:12361620	atgacagaaatgtca[A/C]tgctggggagtgggc	5468
rs1619599	snp	C/T	0.499104	0.0211472	intron-variant	PPARG	GRCh38.p7	3:12462791	AATGCTCTGGGACTT[C/T]TCTTTTAAAAAAAAT	5468
rs1663813	snp	A/G	0	0	intron-variant	PPARG	GRCh38.p7	3:12442980	TTTCTTAGCTGTATC[A/G]CCGTAGGCAAGCCAT	5468
rs1699337	snp	C/T	0.384785	0.210554	intron-variant	PPARG	GRCh38.p7	3:12408594	GCAACAAAGCAAGAC[C/T]CCACCTCAAAAAAAA	5468
rs1699346	snp	A/C	0.499104	0.0211472	intron-variant	PPARG	GRCh38.p7	3:12462796	TTTTAAAAGAGAAGT[A/C]CCAGAGCATTGTGGT	5468
rs1699347	snp	A/G	0.304188	0.244057	intron-variant	PPARG	GRCh38.p7	3:12463276	ctcgctctgcctccc[A/G]ggctggagtgcagta	5468
rs1699348	snp	C/T	0.495213	0.048687	intron-variant	PPARG	GRCh38.p7	3:12466065	CAGCCAACCTCCAAA[C/T]TGCTAAGTAAGCTCC	5468
rs1699366	snp	A/T	0.217551	0.247885	intron-variant	PPARG	GRCh38.p7	3:12446923	AGGCATGAGCCGCCG[A/T]GCTCAGCCCAGTGCA	5468
rs1699373	snp	A/C	0	0	intron-variant	PPARG	GRCh38.p7	3:12420433	AATTGCAGAGGAGAA[A/C]ACAATCACTCTTGTT	5468
rs1797877	snp	A/G	0.081446	0.184634	intron-variant	PPARG	GRCh38.p7	3:12443938	CTGGGTGCCCCACAG[A/G]TACCTCACCCTCAGG	5468
rs1797878	snp	C/T			intron-variant	PPARG	GRCh38.p7	3:12417857	CAAAAGCCAGATTTT[C/T]TTCTGAGTGTGACtt	5468
rs1797879	snp	C/T			intron-variant	PPARG	GRCh38.p7	3:12417860	AAGCCAGATTTTCTT[C/T]TGAGTGTGACttttt	5468
rs1797895	snp	C/G	0	0	intron-variant	PPARG	GRCh38.p7	3:12406315	GATGACCAATACATT[C/G]TTACACTATTCTCAA	5468
rs1797912	snp	A/C	0.416218	0.186739	intron-variant	PPARG	GRCh38.p7	3:12428740	AACCCTGGCAGATCC[A/C]TTTTGCCCTTGACTA	5468
rs1800571	snp	A/C	0	0	PPARG	3	allele_origin=A(germline)/C(germline)	3:12381349	TGGAGCCTGCATCTC[A/C]ACCTTATTATTCTGA	5468
rs1801282	snp	C/G	0.196018	0.244102	PPARG	3	allele_origin=G(germline)/C(germline)	3:12351626	GATTCTCCTATTGAC[C/G]CAGAAAGCGATTCCT	5468
rs1805151	snp	C/T	0	0	utr-variant-3-prime, synonymous-codon, intron-variant	PPARG	GRCh38.p7	3:12434068	GAACAYGTGCAGCTA[C/T]TGCAGGTGATCAAGA	5468
rs1805192	snp	C/G	0	0	PPARG	3	allele_origin=G(germline)/C(germline)	3:12379739	GAGATGCCATTCTGG[C/G]CCACCAACTTTGGGA	5468
rs1822825	snp	C/T	0.495056	0.049474	intron-variant	PPARG	GRCh38.p7	3:12408464	CCTGGATATGAATGG[C/T]TTATTTTCTGTAGTC	5468
rs1875796	snp	C/T	0.494568	0.0518327	intron-variant	PPARG	GRCh38.p7	3:12402158	TAGAACCATGCCTGG[C/T]GCACAATAGTCATTC	5468
rs1899951	snp	A/G	0.380138	0.213458			GRCh38.p7	3:12353341	CTTGGGCCTTTAGGA[A/G]CTCACATTTTTAACA	5468
rs1984669	snp	C/T	0.380333	0.213338	intron-variant	PPARG	GRCh38.p7	3:12334245	TTTCTTTTTTTTTTT[C/T]TTTGAGACAGAGTCT	5468
rs1987536	snp	G/T	0.00383876	0.0436422	intron-variant	PPARG	GRCh38.p7	3:12413006	CTTTGGATGATACTG[G/T]CCAAGCTGATGGAAA	5468
rs2007629	snp	A/G	0.233818	0.249476	intron-variant	PPARG	GRCh38.p7	3:12359862	acatggtgaaacccc[A/G]tctctactaaaaata	5468
rs2012444	snp	A/G	0.126564	0.217402	intron-variant	PPARG	GRCh38.p7	3:12334457	GACCACTTGAGGTCA[A/G]GAGTTCGAGACCAGC	5468
rs2028759	snp	A/G	0.495056	0.049474	intron-variant	PPARG	GRCh38.p7	3:12377113	TGGTTCACTTCATGT[A/G]AACTTGTGAGCCACC	5468
rs2028760	snp	A/G	0.38934	0.207568	intron-variant	PPARG	GRCh38.p7	3:12331383	ACAGATGGAGGAAAT[A/G]AGATGTGAAGGCTGT	5468
rs2067819	snp	A/G	0.306679	0.24349	intron-variant	PPARG	GRCh38.p7	3:12317550	TCTTAGTGATAGCAC[A/G]TAATTTACTAAGCCA	5468
rs2067820	snp	A/G	0.0123036	0.0774623	intron-variant	PPARG	GRCh38.p7	3:12317557	GATAGCACGTAATTT[A/G]CTAAGCCAGTTTTTA	5468
rs2120825	snp	G/T	0.199518	0.24485	intron-variant	PPARG	GRCh38.p7	3:12371840	TCTCAAAACAGCCTT[G/T]TCTGCTGTAGTGTTT	5468
rs2197423	snp	C/T	0.210909	0.246925	intron-variant, upstream-variant-2KB, utr-variant-5-prime	PPARG	GRCh38.p7	3:12350084	AAAGTAATCCAGACA[C/T]GATGGCACAATACTT	5468
rs2197424	snp	C/T			intron-variant	PPARG	GRCh38.p7	3:12375718	AAAAAGTCTGTGCTC[C/T]TAAGGACAGGGCACC	5468
rs2249407	snp	A/C	0.490063	0.0697833	intron-variant	PPARG	GRCh38.p7	3:12453295	GGCCTCCTTAGATAC[A/C]AACACAACAAGTTTT	5468
rs2292101	snp	C/T	0.145642	0.227177	intron-variant	PPARG	GRCh38.p7	3:12393402	GACTTTGGGTGTCAA[C/T]TTAAGGGAAATGATG	5468
rs2307991	in-del	-/ACAGCCATAGCCAC	0.390464	0.206809	intron-variant	PPARG	GRCh38.p7	3:12409619	AAATTGCTCTGCTGC[-/ACAGCCATAGCCAC]TTTTATATACCTCCC	5468
rs2346795	snp	A/G	0.373196	0.217538	intron-variant	PPARG	GRCh38.p7	3:12325564	CGAGATTGCACCACT[A/G]CACTCCAGCCTGGGG	5468
rs2347528	snp	A/T			intron-variant	PPARG	GRCh38.p7	3:12343792	CCATTATCTAATCAT[A/T]ACATCACCCTCATTC	5468
rs2347953	snp	A/G	0.0142736	0.0832652	intron-variant	PPARG	GRCh38.p7	3:12447261	aaagaaaaagagaga[A/G]gagaaagaaagaaaa	5468

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