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
rs4137220	snp	A/T	0.5	0	intron-variant	Rnf121	Mm_Celera	7:102040880	cctacctacctacct[A/T]ccttccttccttcct	75212
rs6224361	snp	A/G	0.408163	0.193609	intron-variant	Rnf121	GRCm38.p3	7:102023451	AGTGACTGAAAGCCA[A/G]ACTGGCACTTTAGCC	75212
rs6225430	snp	A/G	0.444444	0.157135	intron-variant	Rnf121	GRCm38.p3	7:102023631	GTTGGTATGAGCCAA[A/G]ACAGAGAGAATACCC	75212
rs6225445	snp	G/T	0.444444	0.157135	intron-variant	Rnf121	GRCm38.p3	7:102023639	GAGCCAAGACAGAGA[G/T]AATACCCAATACCCA	75212
rs6225481	snp	C/T	0.444444	0.157135	intron-variant	Rnf121	GRCm38.p3	7:102023663	ATACCCAATGTGGCA[C/T]AGAATGGGAGCTTAG	75212
rs6255494	snp	A/G	0.444444	0.157135	intron-variant, upstream-variant-2KB	Xndc1, Xntrpc, Rnf121	GRCm38.p3	7:102071035	CTGCACAGAGAAACC[A/G]TTTTGAAAAACAAAG	75212
rs6268361	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Xndc1, Xntrpc, Rnf121	Mm_Celera	7:102071119	tctgtttttttctct[C/T]tctttctttctttct	75212
rs6268916	snp	A/G	0.21875	0.248039	utr-variant-5-prime, nc-transcript-variant, intron-variant	Xndc1, Xntrpc, Rnf121	Mm_Celera	7:102071238	CAAGAGCAAAACATC[A/G]ACAGTACCACCGTGG	75212
rs6269417	snp	A/G	0.415225	0.187619	synonymous-codon, nc-transcript-variant, intron-variant	Xndc1, Xntrpc, Rnf121	GRCm38.p3	7:102071346	GATCAGCCATGTGGT[A/G]TCATTTTCCTCTCAG	75212
rs6390758	snp	C/T	0.432133	0.171253	intron-variant	Rnf121	GRCm38.p3	7:102057701	GGGAGTTAAATAACA[C/T]AGTAAGTGCTGACAG	75212
rs6390881	snp	A/T	0.42	0.183303	intron-variant	Rnf121	GRCm38.p3	7:102057775	ATTCTGTGTCTATAA[A/T]CCACAGGCAAGGAAC	75212
rs6391466	snp	A/G	0.444444	0.157135	intron-variant	Rnf121	GRCm38.p3	7:102057864	AAAAACACTGGCGTC[A/G]GGACACATGCCTGAC	75212
rs6391475	snp	A/G	0.444444	0.157135	intron-variant	Rnf121	GRCm38.p3	7:102057867	AACACTGGCGTCGGG[A/G]CACATGCCTGACATC	75212
rs13474060	snp	A/T	0.32	0.24	utr-variant-3-prime, upstream-variant-2KB	Rnf121, Il18bp	GRCm38.p3	7:102020255	GGGCCATTCAGGACC[A/T]CCCCAGCTGTGTCTG	75212
rs13474061	snp	C/T			utr-variant-3-prime, upstream-variant-2KB	Rnf121, Il18bp	Mm_Celera	7:102020251	CATTCAGGACCTCCC[C/T]AGCTGTGTCTGGGTT	75212
rs31031412	snp	A/G	0.5	0	intron-variant	Rnf121	GRCm38.p3	7:102040232	TGTCACGAGGAGGAG[A/G]GGGCAGAGGTTACAG	75212
rs31048013	snp	C/T	0.32	0.24	intron-variant	Rnf121	GRCm38.p3	7:102061103	GTTCCAGGTCATTCT[C/T]GGGTATACACTGAGT	75212
rs31052195	snp	G/T	0.5	0	intron-variant	Rnf121	Mm_Celera	7:102037916	CTCATGGGAGCTAAA[G/T]CAGAAGCCACCGTGG	75212
rs31059179	snp	G/T	0.375	0.216506	intron-variant	Rnf121	GRCm38.p3	7:102033546	TTGAACTGGTTCACT[G/T]ATGCCCAAGGCTGAG	75212
rs31093977	snp	C/G	0.432133	0.171253	intron-variant, upstream-variant-2KB	Xndc1, Xntrpc, Rnf121	GRCm38.p3	7:102073788	GGACACACACACACA[C/G]AGCCAAATGTGGTGT	75212
rs31095743	snp	A/C	0.32	0.24	intron-variant	Rnf121	GRCm38.p3	7:102041807	AGCACCCTGAAAAGT[A/C]AGCACCCTGAGAGAA	75212
rs31101882	snp	C/T	0.401235	0.199068	intron-variant	Rnf121	GRCm38.p3	7:102046035	TCTTCCATACTTTTA[C/T]TATGTGTATCTAACT	75212
rs31129168	snp	A/G	0.444444	0.157135	intron-variant, upstream-variant-2KB	Xndc1, Rnf121, Xntrpc	Mm_Celera	7:102066882	GGCATGGTGGCGCAC[A/G]CCTTTAATCCCAGCA	75212
rs31133456	snp	C/G	0.304688	0.243945	intron-variant	Rnf121	GRCm38.p3	7:102053159	GAGATGGAAGCACAG[C/G]GCTGTACTATGTTCA	75212
rs31185766	snp	A/G	0.444444	0.157135	intron-variant	Rnf121	GRCm38.p3	7:102047573	AGAACACCATGATCA[A/G]GGCTGGCAAGATGGC	75212
rs31205669	snp	A/T	0.444444	0.157135	upstream-variant-2KB, utr-variant-5-prime, downstream-variant-500B	Il18bp, Rnf121	GRCm38.p3	7:102019012	CACACACACACACTC[A/T]CACAGAGGGAGGATG	75212
rs31207649	snp	C/G	0.456747	0.140554	intron-variant	Rnf121	GRCm38.p3	7:102022475	TAAGGAGTCCACCCG[C/G]ACAGAGACTTGAAGT	75212
rs31235796	snp	G/T	0.32	0.24	intron-variant	Rnf121	GRCm38.p3	7:102041809	CACCCTGAAAAGTAA[G/T]CACCCTGAGAGAAGT	75212
rs31238760	snp	A/G	0.401235	0.199068	upstream-variant-2KB, intron-variant, utr-variant-3-prime	Il18bp, Rnf121	GRCm38.p3	7:102019428	AGCCTACCTAGGGAC[A/G]TTTCCTGGGCTGGAA	75212
rs31239565	snp	A/G	0.32	0.24	intron-variant, utr-variant-5-prime	Xndc1, Xntrpc, Rnf121	GRCm38.p3	7:102072410	TCTAACTCTCAAGTC[A/G]TCCTGCTTTAACTTC	75212
rs31241226	snp	A/G	0.375	0.216506	intron-variant	Rnf121	GRCm38.p3	7:102054314	TACATGTAGGTATGT[A/G]GTACATAAGCAAGTA	75212
rs31256512	snp	G/T	0.375	0.216506	intron-variant	Rnf121	Mm_Celera	7:102044859	GCTTTCCCTTGGAGG[G/T]GCTTCACCTTCTCTG	75212
rs31274684	snp	C/G	0.48	0.0979796	intron-variant	Rnf121	GRCm38.p3	7:102042516	TGACCCAGATACTTG[C/G]AAAGATTCCCAAAGA	75212
rs31280694	snp	C/T	0.401235	0.199068	intron-variant	Rnf121	Mm_Celera	7:102033884	ATAGAGCATACAAAG[C/T]ACACAAAGCTGTCTG	75212
rs31291752	snp	C/T	0.32	0.24	intron-variant	Rnf121	GRCm38.p3	7:102055282	ACATGCACACACATA[C/T]ACTACACACAACCCA	75212
rs31293274	snp	C/T	0.444444	0.157135	intron-variant	Rnf121	GRCm38.p3	7:102031118	GATGGTACAGGCCCA[C/T]GGTCCCTGCACTGAG	75212
rs31329505	snp	A/G	0.444444	0.157135	intron-variant	Rnf121	GRCm38.p3	7:102037008	GGGCTGCACAGAGAA[A/G]CCCTGTCTCGAAAAA	75212
rs31339660	snp	A/G	0.32	0.24	intron-variant	Rnf121	Mm_Celera	7:102029616	GAGGGCAGGCAGGGC[A/G]TTTATGACCTGGGTA	75212
rs31340696	snp	C/T	0.387812	0.208586	intron-variant	Rnf121	GRCm38.p3	7:102045439	ACCAAAAGGTGACTT[C/T]AATTACATTCAAACC	75212
rs31347922	snp	C/T	0.32	0.24	intron-variant	Rnf121	Mm_Celera	7:102022077	AGGCCACTCTTTCCT[C/T]AAAAGTCTATAGGCA	75212
rs31360755	snp	C/T	0.5	0	intron-variant	Rnf121	Mm_Celera	7:102051594	AGATGGTCCCTATGT[C/T]GGTTTGAATGAAACA	75212
rs31372735	snp	A/T	0.415225	0.187619	intron-variant	Rnf121	GRCm38.p3	7:102040270	GTCTTAGACTCTTAC[A/T]ATTTATCACACACTA	75212
rs31388887	snp	C/G	0.444444	0.157135	intron-variant	Rnf121	GRCm38.p3	7:102053055	AATAATGAATGTGGA[C/G]TCAAATATATACACA	75212
rs31438004	snp	A/G	0.375	0.216506	intron-variant	Rnf121	GRCm38.p3	7:102033675	ATCATTTTAAAAGAA[A/G]TTGAACATTTATCAC	75212
rs31477292	snp	C/T	0.33241	0.236027	intron-variant	Rnf121	GRCm38.p3	7:102023226	ATTTAGGACATCCCA[C/T]TTCCCTAGAACAGAA	75212
rs31483599	snp	A/C	0.33241	0.236027	intron-variant	Rnf121	GRCm38.p3	7:102052738	TATTTATACTTATGC[A/C]AATCATCTCAGCTCT	75212
rs31495116	snp	A/G	0.32	0.24	intron-variant	Rnf121	GRCm38.p3	7:102044936	TTGGAAGGGGGCTGC[A/G]ATTATGATAAAAAGC	75212
rs31514099	snp	A/C/G	0.304688	0.243945	intron-variant	Rnf121	GRCm38.p3	7:102058866	CCCAAACGAAAGCAA[A/C/G]GGTGAGCTGGGAGTT	75212
rs31540861	snp	C/T	0.33241	0.236027	intron-variant	Rnf121	GRCm38.p3	7:102058992	TTGTTTACTCCTTCA[C/T]TACCATGAGTCTTTT	75212
rs31589675	snp	C/T	0.32	0.24	intron-variant, upstream-variant-2KB	Xndc1, Xntrpc, Rnf121	Mm_Celera	7:102072814	GTATAGTGTTAAGAG[C/T]TCTATTTTAGGAACT	75212
rs31598282	snp	G/T	0.387812	0.208586	intron-variant	Rnf121	GRCm38.p3	7:102042001	TCAAAGCAAGTACAC[G/T]GGAAGCTTACCAGTG	75212
rs31613432	snp	G/T	0.415225	0.187619	intron-variant	Rnf121	GRCm38.p3	7:102040365	GGTCTAGAGGGCTTA[G/T]GACTAACTAAAGGTT	75212
rs31635926	snp	C/T	0.444444	0.157135	intron-variant	Rnf121	GRCm38.p3	7:102047590	GCTGGCAAGATGGCT[C/T]GGCAGGTAAGAGCCC	75212
rs31641857	snp	C/T	0.32	0.24	intron-variant	Rnf121	GRCm38.p3	7:102022215	CAGGGAGTTTTAGGC[C/T]TGTGACTTTCAGCAG	75212
rs31657670	snp	G/T	0.375	0.216506	intron-variant	Rnf121	GRCm38.p3	7:102044274	ACTTCAACCCAAAAT[G/T]TGTCCTGCCTACAAA	75212
rs31670875	snp	A/G	0.444444	0.157135	intron-variant	Rnf121	GRCm38.p3	7:102031067	AATCAGTTTCAGACA[A/G]TTAACAAATTATATG	75212
rs31672677	snp	C/T	0.32	0.24	intron-variant	Rnf121	GRCm38.p3	7:102044608	CCACCAACTAAAGAA[C/T]ATGCAGGAACTGGAC	75212
rs31692580	snp	A/C	0.444444	0.157135	intron-variant	Rnf121	GRCm38.p3	7:102026072	TGGTGCACAGTGATA[A/C]ATGCAGGCAAAATAC	75212
rs31707077	snp	A/G	0.432133	0.171253	intron-variant	Rnf121	GRCm38.p3	7:102061929	GCTATTCCAGACTAC[A/G]CATGTACTAATGACA	75212
rs31721103	snp	C/T	0.401235	0.199068	intron-variant	Rnf121	GRCm38.p3	7:102050166	GTAGATCAATTATCA[C/T]TTCCTTTGTGTAATA	75212
rs31737838	snp	A/G	0.375	0.216506	intron-variant	Rnf121	GRCm38.p3	7:102059386	CACACTGACACAGTG[A/G]GAACAGTAGTGCAGA	75212
rs31741183	snp	A/G	0.444444	0.157135	intron-variant	Xndc1, Xntrpc, Rnf121	GRCm38.p3	7:102071816	TGACAGTACTACTAC[A/G]TGGTGATTATGACAA	75212
rs31742470	snp	C/T	0.32	0.24	intron-variant	Rnf121	GRCm38.p3	7:102021514	GTAAAATAGATACAC[C/T]ACCTTCTCAGAAATG	75212
rs31756958	snp	C/G	0.444444	0.157135	upstream-variant-2KB, utr-variant-5-prime, downstream-variant-500B	Il18bp, Rnf121	Mm_Celera	7:102019017	ACACACACTCTCACA[C/G]AGGGAGGATGGGTGA	75212
rs31761480	snp	A/G	0.444444	0.157135	intron-variant	Rnf121	Mm_Celera	7:102031119	ATGGTACAGGCCCAC[A/G]GTCCCTGCACTGAGG	75212
rs31771168	snp	A/G	0.32	0.24	intron-variant	Rnf121	GRCm38.p3	7:102051885	TAAGTCAAAATAAAC[A/G]CTTTCTTTTGCCTTA	75212
rs31786861	snp	C/T	0.444444	0.157135	intron-variant	Rnf121	GRCm38.p3	7:102054167	AATAAATCTGTTATA[C/T]GGATGGTTGTGAGCT	75212
rs31789565	snp	A/T	0.415225	0.187619	intron-variant	Rnf121	GRCm38.p3	7:102040187	AATGCCAGAAGCTAG[A/T]GTCAGTGCCATTTCA	75212
rs31796223	snp	C/T	0.375	0.216506	intron-variant, upstream-variant-2KB	Xndc1, Xntrpc, Rnf121	GRCm38.p3	7:102073554	AAAGCTAGGCATGGG[C/T]CTGGGAGACTGCTCA	75212
rs31806278	snp	A/G	0.375	0.216506	intron-variant	Rnf121	Mm_Celera	7:102029798	CTCTCTTGACCTATA[A/G]AGACTTTATCTAATA	75212
rs31806296	snp	C/T	0.387812	0.208586	intron-variant	Rnf121	GRCm38.p3	7:102038958	AAGATTTCCGATATT[C/T]CCTTCATGAATCTGT	75212
rs31807550	snp	A/G	0.375	0.216506	intron-variant	Rnf121	GRCm38.p3	7:102041010	GCCTCCAGATTCCTG[A/G]GATTAAAGGTATGCA	75212
rs31817048	snp	A/T	0.375	0.216506	intron-variant	Rnf121	GRCm38.p3	7:102044782	CCTAAGTGGGAGAAG[A/T]TGTGCTTAGTCCTTC	75212
rs31824278	snp	A/C	0.375	0.216506	intron-variant	Rnf121	GRCm38.p3	7:102047349	TACCCACTGTGCCAT[A/C]TCATTGACACTTGAG	75212
rs31836626	snp	C/T	0.35503	0.226867	intron-variant	Rnf121	GRCm38.p3	7:102028336	TTTAACATTTACCTT[C/T]CTCATTAATGAGTAC	75212
rs31836629	snp	A/G	0.231111	0.249285	intron-variant	Rnf121	Mm_Celera	7:102028399	ATACTCAGATTTTAT[A/G]TGTAGGACAAAGTGA	75212
rs31836632	snp	A/C	0.391111	0.206368	intron-variant	Rnf121	GRCm38.p3	7:102028739	GCTAGTTGGAACAAT[A/C]TGGAGTAACAAGCAG	75212
rs31836764	snp	C/T	0.124444	0.216185	intron-variant	Rnf121	Mm_Celera	7:102021393	CTAGTAAAAATCAAG[C/T]TACCCAGATTCTCTT	75212
rs31836766	snp	A/G	0.459184	0.136902	intron-variant	Rnf121	GRCm38.p3	7:102021432	TAGGTTGGAATGAAA[A/G]GCTGAACCCAGAAAA	75212
rs31836771	snp	A/G	0.456747	0.140554	intron-variant	Rnf121	GRCm38.p3	7:102021586	AAACCCATGGCAGAA[A/G]AGGCTGGGAATAGGT	75212
rs31836776	snp	A/T	0.336735	0.234472	intron-variant	Rnf121	GRCm38.p3	7:102051242	CCTACTCACAGGGGG[A/T]TTCTTTTATGATGAT	75212
rs31836779	snp	C/T	0.32	0.24	intron-variant	Rnf121	GRCm38.p3	7:102051947	AACCTAATACAGTCC[C/T]TGATTTACATTTTTA	75212
rs31836805	snp	G/T	0.429688	0.173817	intron-variant	Rnf121	GRCm38.p3	7:102036055	TCTCTATATGAGATG[G/T]GCTTTGTTCAGTTTG	75212
rs31836808	snp	A/G	0.391111	0.206368	intron-variant	Rnf121	GRCm38.p3	7:102036461	TAGCACCCCTAGCAA[A/G]TGGCCATCTTTATTT	75212
rs31836810	snp	A/G	0.391111	0.206368	intron-variant	Rnf121	GRCm38.p3	7:102037467	GCATTATTTTGCAGA[A/G]TCCCAGGTGGACAAG	75212
rs31836812	snp	A/G	0.124444	0.216185	intron-variant	Rnf121	Mm_Celera	7:102037486	CAGGTGGACAAGTCT[A/G]CTGCTCATCACTCCA	75212
rs31837235	snp	A/T	0.124444	0.216185	upstream-variant-2KB, intron-variant	Xndc1, Rnf121, Xntrpc	Mm_Celera	7:102065249	CGGATGCCTGTGAGG[A/T]ACCTAGAGACCGTCT	75212
rs31837237	snp	A/T	0.391111	0.206368	upstream-variant-2KB, intron-variant, utr-variant-5-prime	Xndc1, Rnf121, Xntrpc	GRCm38.p3	7:102065283	TGCTCCTTCGGAATT[A/T]AGAAGGGGCGACTCG	75212
rs31837239	snp	C/G	0.152778	0.230321	upstream-variant-2KB, intron-variant, utr-variant-5-prime	Xndc1, Rnf121, Xntrpc	GRCm38.p3	7:102065411	AGGAAAAGGGAGAGT[C/G]CCTGAATGCGCAAAT	75212
rs31837242	snp	C/T	0.391111	0.206368	upstream-variant-2KB, intron-variant, utr-variant-5-prime	Xndc1, Rnf121, Xntrpc	GRCm38.p3	7:102065442	TTCGCGACACTCCCT[C/T]GCTTAGGACACGAGC	75212
rs31837425	snp	A/G	0.124444	0.216185	intron-variant	Rnf121	Mm_Celera	7:102029004	CACGCACGCACAGAT[A/G]AGCTTACCCCTATGG	75212
rs31837427	snp	A/T	0.336735	0.234472	intron-variant	Rnf121	GRCm38.p3	7:102029156	GAAGCAGCATGGCAG[A/T]AAGGCCTGCTCTGAG	75212
rs31837430	snp	A/G	0.408163	0.193609	intron-variant	Rnf121	GRCm38.p3	7:102029329	GAGAAAGCCATTACT[A/G]TGAGCTGCAAAAACC	75212
rs31837433	snp	A/T	0.142012	0.225474	intron-variant	Rnf121	Mm_Celera	7:102029405	TCTGGCTGTAGTTCC[A/T]GCCTGATGTGACAGG	75212
rs31837524	snp	C/G	0.444444	0.157135	intron-variant	Rnf121	Mm_Celera	7:102021819	TAACTATATTCCTGG[C/G]CCCCAGAAGGTTCTT	75212
rs31837527	snp	A/G	0.124444	0.216185	intron-variant	Rnf121	Mm_Celera	7:102022441	CAGTCAGAGAGAAAA[A/G]GAGCCAACAGGTTAT	75212
rs31837531	snp	C/T	0.459184	0.136902	intron-variant	Rnf121	GRCm38.p3	7:102022700	AGCTAAGGGCAGCCA[C/T]AAACCCCAGCAAGGC	75212
rs31837574	snp	A/G	0.391111	0.206368	intron-variant	Rnf121	GRCm38.p3	7:102052767	CTCCAGAAGCACACG[A/G]AGGAGGATCACAGGT	75212
rs31837578	snp	C/T	0.489796	0.070696	intron-variant	Rnf121	GRCm38.p3	7:102053535	CTTTCCATTCTGCTG[C/T]ACTACTCTTAACACA	75212
rs31837581	snp	A/G	0.297521	0.245442	intron-variant	Rnf121	Mm_Celera	7:102055321	CTCTAGTACAAGTCT[A/G]TCTGTCTGTCTGTCT	75212

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