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
rs4188874	snp	A/C	0.476371	0.106096	intron-variant	Tfg	Mm_Celera	16:56691566	GTACCACATGAAATC[A/C]CATTACAGACAAGTG	21787
rs4188875	snp	C/T	0.401235	0.199068	intron-variant	Tfg	Mm_Celera	16:56693562	TCTATAGCTAGCCAT[C/T]TATCTATCTGCAATT	21787
rs4188876	snp	C/T	0.4992	0.019984	intron-variant	Tfg	Mm_Celera	16:56693860	CTCAGGCGATGCAGA[C/T]TTCTATGTGTTGAAA	21787
rs4188877	snp	C/G	0.4992	0.019984	intron-variant	Tfg	Mm_Celera	16:56693906	ACTGTGCCACTTCAC[C/G]TCAGCACAGTTAAAA	21787
rs4188878	snp	C/T	0.444444	0.157135	intron-variant	Tfg	Mm_Celera	16:56695680	TGTCTACAATGTATA[C/T]ATTATATATCAAGAG	21787
rs4188879	snp	A/G	0.375	0.216506	intron-variant	Tfg	GRCm38.p3	16:56695696	ATTATATATCAAGAG[A/G]TATTCACTAAAGCAG	21787
rs4188880	snp	C/T	0.5	0	intron-variant	Tfg	GRCm38.p3	16:56703934	TTTACATTTGAAACA[C/T]AGTTTTTACTACAGA	21787
rs4231231	snp	A/G	0.244898	0.249948	intron-variant	Tfg	GRCm38.p3	16:56691331	TAGAATTTAAAAAGT[A/G]TCTGGAAAAATTTTG	21787
rs4231232	snp	A/G	0.244898	0.249948	intron-variant	Tfg	GRCm38.p3	16:56691224	TTTTGGTCCATAGCA[A/G]TAAGACTAAGTCTCT	21787
rs4231233	snp	A/G	0.244898	0.249948	intron-variant	Tfg	GRCm38.p3	16:56691214	TAGCAATAAGACTAA[A/G]TCTCTGGAAAACTTT	21787
rs4231234	snp	A/G	0.244898	0.249948	intron-variant	Tfg	GRCm38.p3	16:56691192	GAAAACTTTCACCAA[A/G]AAACCCAAAACATTT	21787
rs4231235	snp	A/G	0.244898	0.249948	intron-variant	Tfg	GRCm38.p3	16:56691171	CAAAACATTTGTTAT[A/G]TATTTTGCTTTTTTC	21787
rs13475551	snp	A/G	0.231111	0.249285	synonymous-codon	Tfg	GRCm38.p3	16:56701184	TGACTCTTCTGGGAA[A/G]CAGTCAACTCAGGTT	21787
rs45689701	snp	A/C	0.48	0.0979796	intron-variant	Tfg	Mm_Celera	16:56693552	CTATAGTCTATCTAT[A/C]GCTAGCCATCTATCT	21787
rs45720976	snp	C/T	0.231111	0.249285	intron-variant	Tfg	GRCm38.p3	16:56705082	ACCCATCATTGTTAG[C/T]TTTTACTCCCTGAAA	21787
rs45731254	snp	C/T	0.32	0.24	intron-variant	Tfg	GRCm38.p3	16:56696746	GTCATCTGTGCCAAA[C/T]AGCCCTTTTAAATAC	21787
rs45765073	snp	A/C	0.231111	0.249285	intron-variant	Tfg	Mm_Celera	16:56693179	TTTCCTTTAAAATCA[A/C]TTCATCTGTTTTTTG	21787
rs45774011	snp	C/T	0.231111	0.249285	intron-variant	Tfg	GRCm38.p3	16:56695658	AGTCAATCTAAATAA[C/T]TGGCAGTGTCTACAA	21787
rs45965124	snp	A/T	0.277778	0.248452	intron-variant	Tfg	Mm_Celera	16:56697022	AATCAGTGAAAAAAA[A/T]ATCAAAACTCAGATA	21787
rs46046760	snp	A/C			intron-variant	Tfg	Mm_Celera	16:56695996	CAAAGAGAATGCATC[A/C]GTAGTAGTAATGTGA	21787
rs46097124	snp	G/T			intron-variant	Tfg	Mm_Celera	16:56696003	AATGCATCAGTAGTA[G/T]TAATGTGAAGCTGCT	21787
rs46128132	snp	C/T	0.231111	0.249285	intron-variant	Tfg	GRCm38.p3	16:56692396	ATTTCTCCCGTCTTC[C/T]ATACTAAACTTAAAT	21787
rs46235667	snp	A/T	0.132653	0.220748	intron-variant	Tfg	Mm_Celera	16:56712395	GAACATACATGTGGA[A/T]ATCTGAGCAGAAGAA	21787
rs46362641	snp	G/T			intron-variant	Tfg	GRCm38.p3	16:56696014	GTAGTAATGTGAAGT[G/T]GCTGGAAAGAGGTGC	21787
rs46388011	snp	A/G	0.231111	0.249285	intron-variant	Tfg	Mm_Celera	16:56695815	CGTATGGTGTTTAAA[A/G]TGTTCCAAATCACTG	21787
rs46466240	snp	C/T	0.231111	0.249285	intron-variant	Tfg	GRCm38.p3	16:56692907	CTGACCACTCAAGTC[C/T]AGATTGGAGACTATA	21787
rs46492212	snp	C/T	0.124444	0.216185	intron-variant	Tfg	Mm_Celera	16:56698485	GATGTGAAGAGTTCC[C/T]GGAGCTAATTATTAG	21787
rs46528311	snp	A/G	0.444444	0.157135	intron-variant	Tfg	Mm_Celera	16:56694243	CATCTCTATAATTAC[A/G]TTGAATTTGCTCACT	21787
rs46533767	snp	C/T	0.142012	0.225474	intron-variant	Tfg	GRCm38.p3	16:56707221	TGCCATCTCATGTAG[C/T]TGCTAACAGACTATG	21787
rs46551187	snp	C/T	0.231111	0.249285	intron-variant	Tfg	GRCm38.p3	16:56704017	AAAAGTGTTTGAAAA[C/T]TGGCCTACTGTACAG	21787
rs46555295	snp	A/G	0.18	0.24	intron-variant	Tfg	Mm_Celera	16:56716099	TTGCTTAACCTGAGA[A/G]GAGGCCCTCTTTCAG	21787
rs46652252	snp	C/T	0.231111	0.249285	intron-variant	Tfg	GRCm38.p3	16:56692681	AATAAAACTATCTTT[C/T]CATCCTACACCTGAA	21787
rs46746244	snp	A/T	0.260355	0.249785	intron-variant	Tfg	Mm_Celera	16:56706203	GGGAAGAGTTTCATA[A/T]ATTAGTAGCATGAGC	21787
rs46748049	snp	G/T	0.124444	0.216185	intron-variant	Tfg	Mm_Celera	16:56716691	TAACTCCAGGTCTAC[G/T]CTCCAACGTCCAAGC	21787
rs46786590	snp	A/G	0.124444	0.216185	upstream-variant-2KB	Tfg	Mm_Celera	16:56718658	CTATAGATGTAATTT[A/G]AGCATACTTTTTATT	21787
rs46816358	snp	A/G	0.231111	0.249285	intron-variant	Tfg	GRCm38.p3	16:56698910	GAGGAAGAAAGAGGA[A/G]TGGGCTCTTGAGAGC	21787
rs46819057	snp	A/C	0.142012	0.225474	intron-variant	Tfg	Mm_Celera	16:56705569	ATCTAATAGCATTTC[A/C]GTCCAAAAATAAATA	21787
rs47053490	snp	G/T	0.32	0.24	intron-variant	Tfg	GRCm38.p3	16:56701401	AACAGTTTTCCAAAA[G/T]AATTATTGTCTCTAA	21787
rs47062538	snp	A/G	0.124444	0.216185	intron-variant	Tfg	Mm_Celera	16:56700087	AGGATGAAGCTCCCT[A/G]TCAGTGAAGGCCTAG	21787
rs47112020	snp	C/T	0.231111	0.249285	intron-variant	Tfg	Mm_Celera	16:56698820	CTGACAAGAAGTGTT[C/T]GAAACGAGTGCTTGG	21787
rs47235825	snp	C/T	0.231111	0.249285	intron-variant	Tfg	GRCm38.p3	16:56716544	TACAATTCTCCCTAC[C/T]GTGCCCAGAGACGGC	21787
rs47252583	snp	C/T	0.444444	0.157135	intron-variant	Tfg	GRCm38.p3	16:56697104	CCTCAAATGAATTGA[C/T]CCAAATCTACATTCT	21787
rs47374639	snp	A/G	0.124444	0.216185	intron-variant	Tfg	Mm_Celera	16:56716463	GTTCTTCTCTGCGGC[A/G]TACTTTCTGCACATG	21787
rs47438255	snp	A/G	0.231111	0.249285	intron-variant	Tfg	GRCm38.p3	16:56692170	TCTCCATGCAGAGTA[A/G]TTAGTTATCTATTTC	21787
rs47482130	snp	C/T	0.497778	0.0332592	intron-variant	Tfg	GRCm38.p3	16:56697344	ACCATGTCAGTAAGA[C/T]AGACTATTTTCCATC	21787
rs47492664	snp	A/G	0.444444	0.157135	intron-variant	Tfg	GRCm38.p3	16:56694884	CATTACAAGTCATTT[A/G]GATTTTAGCAACTAT	21787
rs47554104	snp	C/T	0.231111	0.249285	intron-variant	Tfg	GRCm38.p3	16:56698977	TCACTTCCTTGTTTA[C/T]TTGCCTTCTGACCAC	21787
rs47626905	snp	A/G	0.32	0.24	upstream-variant-2KB	Tfg	GRCm38.p3	16:56718739	GAAAGAAGAGGTTGT[A/G]GATTTTGTAGCAGTG	21787
rs47632052	snp	A/C	0.32	0.24	intron-variant	Tfg	GRCm38.p3	16:56698084	ATTAACTGCAACAGT[A/C]ACATACTTAAATGGC	21787
rs47634203	snp	C/G	0.497778	0.0332592	intron-variant	Tfg	GRCm38.p3	16:56692981	CTGAATATCTGCATG[C/G]CTTGAAAAGCCACTT	21787
rs47804468	snp	C/T	0.124444	0.216185	upstream-variant-2KB	Tfg	Mm_Celera	16:56718993	AGTCTAGAACACATC[C/T]CTTCTCTATTGCTGT	21787
rs47834089	snp	G/T	0.124444	0.216185	intron-variant	Tfg	Mm_Celera	16:56703332	CCCTGAGTCTGATAC[G/T]CAAAGGCAGAGATTG	21787
rs47916312	snp	A/G			intron-variant	Tfg	Mm_Celera	16:56695786	AACTAGAGCTAGTTC[A/G]AACTGGGACATAACG	21787
rs47989070	snp	A/G	0.152778	0.230321	intron-variant	Tfg	Mm_Celera	16:56706055	CTCAGAGATGTAACA[A/G]TATCACAAATTACTA	21787
rs48040497	snp	A/G	0.124444	0.216185	intron-variant	Tfg	Mm_Celera	16:56692965	CTGTTCAGCCTCCTC[A/G]CTGAATATCTGCATG	21787
rs48049231	snp	C/T	0.124444	0.216185	intron-variant	Tfg	Mm_Celera	16:56716698	AGGTCTACGCTCCAA[C/T]GTCCAAGCCACTCCC	21787
rs48061034	snp	C/T	0.42	0.183303	intron-variant	Tfg	Mm_Celera	16:56692842	TTGCAACAAAATAGG[C/T]AATAGATATTTTTTA	21787
rs48066510	snp	C/T	0.244898	0.249948	intron-variant	Tfg	Mm_Celera	16:56695454	AAGCTTAGGTATATG[C/T]TTGCCTGAGCCTTCC	21787
rs48087395	snp	G/T	0.231111	0.249285	intron-variant, synonymous-codon	Tfg	GRCm38.p3	16:56704443	ATTTTCAGGAATACT[G/T]GTGGAAGGTCCTGGT	21787
rs48184276	snp	C/T	0.497778	0.0332592	utr-variant-3-prime, downstream-variant-500B	Abi3bp, Tfg	GRCm38.p3	16:56689895	CATGAATGAATGTAT[C/T]ACAGAATGTTTTTGT	21787
rs48257217	snp	C/T	0.32	0.24	upstream-variant-2KB	Tfg	GRCm38.p3	16:56718780	ACTTTAGTACTGTTG[C/T]TTGTCTGCTTTCAGG	21787
rs48470946	snp	A/G	0.32	0.24	intron-variant	Tfg	GRCm38.p3	16:56704351	ACCTGACTCCAAGAA[A/G]CAATCAAATAATCCT	21787
rs48543884	snp	A/G	0.277778	0.248452	intron-variant	Tfg	Mm_Celera	16:56706080	TTACTATATTAGACT[A/G]AAAAATCTTTCCATT	21787
rs48558331	snp	C/G	0.444444	0.157135	upstream-variant-2KB	Tfg	GRCm38.p3	16:56717612	CTTCCGGTTTTCCGG[C/G]CAGCCAGTCTTTCCT	21787
rs48741213	snp	A/G			intron-variant	Tfg	Mm_Celera	16:56696049	GTTGCTAGAACACAG[A/G]TGGAAGACCATTTTC	21787
rs48759912	snp	A/G	0.231111	0.249285	intron-variant	Tfg	Mm_Celera	16:56697801	TAGAAATGCTTCCCT[A/G]CAAATGTGTGAAATG	21787
rs48801532	snp	A/T	0.231111	0.249285	intron-variant	Tfg	Mm_Celera	16:56698970	GCCCCTTTCACTTCC[A/T]TGTTTATTTGCCTTC	21787
rs48850140	snp	C/T	0.231111	0.249285	intron-variant	Tfg	GRCm38.p3	16:56693931	TTAAAACACTGAATA[C/T]TCTTAGTTGCCTGAA	21787
rs48980547	snp	C/T	0.231111	0.249285	synonymous-codon, downstream-variant-500B	Tfg	GRCm38.p3	16:56690969	AGTATAGTTGGCAGG[C/T]TGAGATGGTTGGGTA	21787
rs49021427	snp	A/G	0.231111	0.249285	intron-variant	Tfg	GRCm38.p3	16:56693711	CTGATGAAACTAGAA[A/G]AAATACCTAAATTAT	21787
rs49052699	snp	C/T	0.32	0.24	upstream-variant-2KB	Tfg	GRCm38.p3	16:56718921	TTGCTTATTCCTTTA[C/T]AATGTCTTGTGATCT	21787
rs49139517	snp	A/G	0.124444	0.216185	intron-variant	Tfg	Mm_Celera	16:56704608	TTGCTTAAACTTAGG[A/G]AATGATGCCATTAAA	21787
rs49193740	snp	C/G	0.244898	0.249948	intron-variant	Tfg	Mm_Celera	16:56692788	TACACCCTCCTAACA[C/G]TCCTAAAATGAGTAA	21787
rs49194518	snp	A/C	0.231111	0.249285	intron-variant	Tfg	Mm_Celera	16:56695507	ACAATCAGTAGCAAA[A/C]CATACTTCGGGGGAA	21787
rs49213756	snp	C/G	0.426035	0.177515	intron-variant	Tfg	Mm_Celera	16:56695400	ATTGGCTGGTCTCTC[C/G]TTTTTTCACTTTTCA	21787
rs49222015	snp	G/T	0.231111	0.249285	downstream-variant-500B	Abi3bp, Tfg	GRCm38.p3	16:56690191	CGTAAGGAAAAATCA[G/T]AAAATGAAGAGCTAC	21787
rs49230681	snp	C/T	0.277778	0.248452	intron-variant	Tfg	GRCm38.p3	16:56692929	GAGACTATAAAACGG[C/T]ATAAAGACAAGAGAA	21787
rs49368973	snp	A/G	0.444444	0.157135	intron-variant	Tfg	GRCm38.p3	16:56698001	AATGATCCACTTCAT[A/G]GTTTCATAGGATGTC	21787
rs49542158	snp	A/G	0.375	0.216506	intron-variant	Tfg	GRCm38.p3	16:56709707	TGACAATGTATATTA[A/G]CATAATGAACACCAA	21787
rs49546902	snp	C/T	0.408163	0.193609	upstream-variant-2KB	Tfg	Mm_Celera	16:56718661	TAGATGTAATTTGAG[C/T]ATACTTTTTATTAAA	21787
rs49547648	snp	A/G	0.124444	0.216185	intron-variant	Tfg	Mm_Celera	16:56716646	TGTACGACCGAATGG[A/G]GCTCCTTTCTGTGTC	21787
rs49551515	snp	C/T	0.132653	0.220748	intron-variant	Tfg	Mm_Celera	16:56693104	AATGTCTATATGTTA[C/T]ACAATTTGTACCATA	21787
rs49554164	snp	C/T	0.231111	0.249285	intron-variant	Tfg	GRCm38.p3	16:56700027	AGAATTTCAAGACAA[C/T]CATCATGGTAACAAT	21787
rs49618972	snp	C/T	0.231111	0.249285	intron-variant, synonymous-codon	Tfg	GRCm38.p3	16:56704470	TGGTTCTCCAGGTGG[C/T]TCTAAGCTATCCAAT	21787
rs49657926	snp	A/G	0.231111	0.249285	upstream-variant-2KB	Tfg	GRCm38.p3	16:56718979	TCATCTAAACTCCCA[A/G]TCTAGAACACATCCC	21787
rs49665366	snp	A/G	0.32	0.24	upstream-variant-2KB	Tfg	GRCm38.p3	16:56718893	TGGCCTGAAATTCAG[A/G]GTTTTCCTTGTCTTG	21787
rs49671924	snp	C/T	0.142012	0.225474	intron-variant	Tfg	Mm_Celera	16:56707488	ACTCATCAAAAATGA[C/T]GGTTGTATGACAGAA	21787
rs49720676	snp	C/T	0.408163	0.193609	upstream-variant-2KB	Tfg	GRCm38.p3	16:56718603	TGTCCTAGACATGGA[C/T]ACAGTTCCCTATAGT	21787
rs49730130	snp	C/T	0.444444	0.157135	intron-variant	Tfg	Mm_Celera	16:56692926	TTGGAGACTATAAAA[C/T]GGTATAAAGACAAGA	21787
rs49732444	snp	A/T	0.231111	0.249285	intron-variant	Tfg	Mm_Celera	16:56693013	TAAAAGAGTAGAACA[A/T]CATCAGTGGTCCTCA	21787
rs49752601	snp	A/G	0.124444	0.216185	intron-variant	Tfg	Mm_Celera	16:56698259	TTTCCTTAAGACTGT[A/G]AGAACTTTGGCCATA	21787
rs49774320	snp	C/G	0.231111	0.249285	downstream-variant-500B, utr-variant-3-prime	Abi3bp, Tfg	Mm_Celera	16:56690404	TCATCTTCTCAGAGG[C/G]CTCTATTTTTAGTAC	21787
rs49775485	snp	C/T	0.124444	0.216185	intron-variant	Tfg	Mm_Celera	16:56701331	TAAATACTGTCAGGA[C/T]TTTGTGAATATAGAA	21787
rs49945457	snp	A/C	0.132653	0.220748	intron-variant	Tfg	GRCm38.p3	16:56694995	ACTCACTGTGTAATA[A/C]CCTAGTGATGTTGGA	21787
rs50009659	snp	A/G	0.32	0.24	intron-variant	Tfg	GRCm38.p3	16:56699505	CGCACACAGTTTCCC[A/G]AGAGAAGATACTGTA	21787
rs50058533	snp	G/T	0.124444	0.216185	intron-variant	Tfg	Mm_Celera	16:56716472	TGCGGCGTACTTTCT[G/T]CACATGCGAAGGGAG	21787
rs50159047	snp	C/T	0.231111	0.249285	intron-variant	Tfg	GRCm38.p3	16:56705376	GATTCCTAAGTTACA[C/T]TCATCTCAAAACCAA	21787
rs50172536	snp	C/G	0.231111	0.249285	intron-variant	Tfg	GRCm38.p3	16:56699642	ACATTACTGTGGTAG[C/G]TATTTCCCACCTTAA	21787
rs50189923	snp	A/G	0.231111	0.249285	intron-variant	Tfg	GRCm38.p3	16:56691538	TAGGTTTAAAGGGAA[A/G]TCCTATTTAACAGTA	21787
rs50231035	snp	C/T	0.231111	0.249285	intron-variant	Tfg	GRCm38.p3	16:56695717	ACTAAAGCAGCTTAT[C/T]CTACATCACTATCTC	21787

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