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
rs3704347	snp	C/T	0.455	0.143091	intron-variant	Rcbtb2	GRCm38.p3	14:73168777	TGAAAGCTTCTGGCT[C/T]CTTTGGATAGTCACG	105670
rs4230464	snp	A/G	0.21875	0.248039	intron-variant	Rcbtb2	Mm_Celera	14:73178283	AACG[A/G]	105670
rs4230465	snp	A/G	0.21875	0.248039	intron-variant	Rcbtb2	Mm_Celera	14:73178295	CTCAGCTGTCTTCCC[A/G]GGGTGCTGTGAAGGC	105670
rs4230466	snp	A/G	0.21875	0.248039	intron-variant	Rcbtb2	Mm_Celera	14:73178298	AGCTGTCTTCCCGGG[A/G]TGCTGTGAAGGCGGC	105670
rs4230467	snp	C/G	0.21875	0.248039	intron-variant	Rcbtb2	Mm_Celera	14:73178312	GGTGCTGTGAAGGCG[C/G]CTTCAGAGTTGCAGA	105670
rs4230468	snp	A/T	0.375	0.216506	intron-variant	Rcbtb2	Mm_Celera	14:73178319	TGAAGGCGGCTTCAG[A/T]GTTGCAGAGCTCATT	105670
rs4230469	snp	C/T	0.375	0.216506	intron-variant	Rcbtb2	Mm_Celera	14:73178321	AAGGCGGCTTCAGAG[C/T]TGCAGAGCTCATTTT	105670
rs4230470	snp	C/G	0.21875	0.248039	intron-variant	Rcbtb2	Mm_Celera	14:73178326	GGCTTCAGAGTTGCA[C/G]AGCTCATTTTGCCCG	105670
rs4230472	snp	A/G	0.21875	0.248039	intron-variant	Rcbtb2	Mm_Celera	14:73178362	TGGAAGCCCTTCACA[A/G]CCCTCTGAGCACTGC	105670
rs4230473	snp	C/G	0.21875	0.248039	intron-variant	Rcbtb2	Mm_Celera	14:73178377	GCCCTCTGAGCACTG[C/G]ACCTCAATGGTCAGG	105670
rs4230474	snp	C/T	0.21875	0.248039	intron-variant	Rcbtb2	Mm_Celera	14:73178393	ACCTCAATGGTCAGG[C/T]GCTCAGAGCGCACCC	105670
rs4230475	snp	A/G	0.375	0.216506	intron-variant	Rcbtb2	Mm_Celera	14:73178403	TCAGGCGCTCAGAGC[A/G]CACCCACAATACATT	105670
rs4230476	snp	A/C	0.21875	0.248039	intron-variant	Rcbtb2	Mm_Celera	14:73178415	AGCGCACCCACAATA[A/C]ATTCTCCTTTCCATC	105670
rs4230477	snp	C/T	0.21875	0.248039	intron-variant	Rcbtb2	Mm_Celera	14:73178421	CCCACAATACATTCT[C/T]CTTTCCATCAGGGTT	105670
rs4230478	snp	G/T	0.21875	0.248039	synonymous-codon, nc-transcript-variant, intron-variant	Rcbtb2	Mm_Celera	14:73178524	CTGTGAGGAGAATGC[G/T]ATTGCTCTGCTCTCT	105670
rs4230479	snp	A/G	0.21875	0.248039	intron-variant	Rcbtb2	Mm_Celera	14:73178604	CACTAAAAGTAACGT[A/G]TAGCTAGATGAAAAT	105670
rs4230480	snp	C/G	0.21875	0.248039	intron-variant	Rcbtb2	Mm_Celera	14:73178608	AAAAGTAACGTGTAG[C/G]TAGATGAAAATGGAA	105670
rs4230481	snp	C/G	0.21875	0.248039	intron-variant	Rcbtb2	Mm_Celera	14:73178630	AAAATGGAACATACA[C/G]AAATAAAGTCTTAGA	105670
rs4230482	snp	A/G	0.21875	0.248039	intron-variant	Rcbtb2	Mm_Celera	14:73178633	ATGGAACATACAGAA[A/G]TAAAGTCTTAGAGAA	105670
rs4230483	snp	C/T	0.375	0.216506	intron-variant	Rcbtb2	Mm_Celera	14:73178641	TACAGAAATAAAGTC[C/T]TAGAGAACTTATGTG	105670
rs6179146	snp	A/T	0.5	0	intron-variant	Rcbtb2	Mm_Celera	14:73158241	GGGCCTTTGTTCTCC[A/T]GCACCTTGAAGGTTC	105670
rs6179622	snp	C/T	0.5	0	intron-variant	Rcbtb2	GRCm38.p3	14:73158313	AATATATAAAAACCA[C/T]AGAAGGCCACTAATA	105670
rs6192749	snp	G/T	0.5	0	intron-variant	Rcbtb2	Mm_Celera	14:73158449	TGATATGAGGAGGTA[G/T]GTACTTTAAAATAGA	105670
rs6193340	snp	A/G	0.5	0	intron-variant	Rcbtb2	GRCm38.p3	14:73158582	TTTATGTTAAAACTC[A/G]TTGATTTCCAAGTTA	105670
rs6193815	snp	C/T	0.5	0	intron-variant	Rcbtb2	GRCm38.p3	14:73158676	CACATCACTGCAGCT[C/T]CTTGTACATGTGAGA	105670
rs6194340	snp	A/G	0.5	0	intron-variant	Rcbtb2	GRCm38.p3	14:73158776	GCTCTGGTGTTTAGT[A/G]ACTGAAGAAACAGTA	105670
rs6301068	snp	A/G	0.5	0	intron-variant	Rcbtb2	GRCm38.p3	14:73164605	TGGTGGATTCCATCG[A/G]TGGCAATCCAGGCAC	105670
rs6301134	snp	C/T	0.48	0.0979796	intron-variant	Rcbtb2	GRCm38.p3	14:73164657	AAGCACAGGCCGTGA[C/T]GGCTGCTTACCTTCT	105670
rs6301238	snp	A/G	0.5	0	upstream-variant-2KB	Rcbtb2	Mm_Celera	14:73138058	ATGTATGAAGGCAAC[A/G]NTAAGCCCCGGGGAC	105670
rs6301240	snp	G/T	0.5	0	upstream-variant-2KB	Rcbtb2	Mm_Celera	14:73138059	TGTATGAAGGCAACN[G/T]TAAGCCCCGGGGACC	105670
rs6301795	snp	A/G	0.5	0	upstream-variant-2KB	Rcbtb2	Mm_Celera	14:73138136	ctgatcctggagttg[A/G]ctctttggctagact	105670
rs6302667	snp	C/T	0.5	0	intron-variant	Rcbtb2	Mm_Celera	14:73164901	tctctctttctctct[C/T]tctctctctctctct	105670
rs6302862	snp	C/T	0.5	0	upstream-variant-2KB	Rcbtb2	Mm_Celera	14:73138343	aaaggcatgtaccac[C/T]atgcctggcAAAAAG	105670
rs6302926	snp	A/G	0.5	0	upstream-variant-2KB	Rcbtb2	Mm_Celera	14:73138389	AGCTATGTATTGGGG[A/G]AAACATTATAAGTAA	105670
rs13470926	snp	C/T	0.444444	0.157135	utr-variant-5-prime, nc-transcript-variant	Rcbtb2	GRCm38.p3	14:73154325	TCCAGCTTAGCAGAT[C/T]ATACATTCTTCAGGA	105670
rs30153117	snp	A/T	0.48	0.0979796	intron-variant	Rcbtb2	Mm_Celera	14:73174128	TGTCTTTCAGATAAA[A/T]AATATATCTAGAAAC	105670
rs30170712	snp	A/G	0.5	0	intron-variant	Rcbtb2	GRCm38.p3	14:73182448	CATCAAGCTGTTGTT[A/G]TTGTTCCTAGGACTT	105670
rs30275061	snp	C/T	0.375	0.216506	utr-variant-3-prime, nc-transcript-variant	Rcbtb2	Mm_Celera	14:73183662	CTTCTCATAATGGCA[C/T]TGTTGAAAATAAAAC	105670
rs30356833	snp	C/T	0.465374	0.126941	intron-variant	Rcbtb2	GRCm38.p3	14:73170246	TTCCACTGGCTCACT[C/T]TGGAGCAGACTGTGG	105670
rs30360364	snp	C/T	0.5	0	intron-variant	Rcbtb2	GRCm38.p3	14:73145902	AATGTACATTGTTCT[C/T]CCCACCCCCAGTACA	105670
rs30362417	snp	A/T	0.48	0.0979796	intron-variant	Rcbtb2	Mm_Celera	14:73174130	TCTTTCAGATAAAAA[A/T]TATATCTAGAAACAG	105670
rs30385757	snp	A/C/G	0.444444	0.157135	intron-variant	Rcbtb2	GRCm38.p3	14:73145749	TTATCTGGAAGAAGC[A/C/G]TGTGTCTCTTTCAGG	105670
rs30414891	snp	A/G	0.444444	0.157135	intron-variant	Rcbtb2	GRCm38.p3	14:73153877	ACAGGGTTTCTCTGT[A/G]TAGCCCTGGCTGTCC	105670
rs30433102	snp	A/G	0.375	0.216506	intron-variant	Rcbtb2	Mm_Celera	14:73182325	CATGGACTAATTGTT[A/G]ATAATTGCTGTAGCT	105670
rs30447124	snp	C/T	0.5	0	upstream-variant-2KB	Rcbtb2	GRCm38.p3	14:73137733	CTCTGCCACTCTCCA[C/T]GCCCTCTGGGAACTG	105670
rs30474300	snp	A/G	0.5	0	intron-variant	Rcbtb2	GRCm38.p3	14:73144257	GGCGATTAAAGCCGA[A/G]TAAAAGAGACCGAGT	105670
rs30476818	snp	A/C	0.5	0	intron-variant	Rcbtb2	GRCm38.p3	14:73151688	TACACAGGAAGACTG[A/C]CCCAGCAGTAGGAGC	105670
rs30486899	snp	C/T	0.432133	0.171253	upstream-variant-2KB	Rcbtb2	GRCm38.p3	14:73138004	GTATGCATGGGAATG[C/T]GTAAATGTATTCATT	105670
rs30504971	snp	C/T	0.444444	0.157135	intron-variant	Rcbtb2	GRCm38.p3	14:73148375	AAGGTCTTCCTTCCT[C/T]ATCTTGGTTTGTATC	105670
rs30509175	snp	C/G	0.444444	0.157135	intron-variant, utr-variant-5-prime	Rcbtb2	Mm_Celera	14:73143368	TGGACCAGGTCGCTG[C/G]GGTAGCTCTGGGTTC	105670
rs30509830	snp	A/G	0.5	0	intron-variant	Rcbtb2	GRCm38.p3	14:73150006	TTACAGCACAGTCTC[A/G]GGCCTCTTGCTTTTG	105670
rs30522443	snp	A/G	0.32	0.24	intron-variant	Rcbtb2	Mm_Celera	14:73149023	TAGAGTCACAATGGC[A/G]GTGCTCTTGTTTTAG	105670
rs30586648	snp	G/T	0.444444	0.157135	intron-variant	Rcbtb2	Mm_Celera	14:73150181	GGGACCTGGGTTCAA[G/T]TCCCAGCACCCACAT	105670
rs30728361	snp	A/G	0.375	0.216506	intron-variant	Rcbtb2	Mm_Celera	14:73180419	AAAATCCTTAAATAC[A/G]CTGAAGCTCTAGTGA	105670
rs30736436	snp	A/G	0.5	0	intron-variant	Rcbtb2	GRCm38.p3	14:73160294	AATGGGATTGGGCCT[A/G]GTATTCCTTGTTTTA	105670
rs30750155	snp	A/G	0.5	0	intron-variant	Rcbtb2	GRCm38.p3	14:73177784	ATGTATGTCCCCACA[A/G]TACACTCTGGGTGAG	105670
rs30766073	snp	A/G	0.5	0	utr-variant-3-prime, nc-transcript-variant	Rcbtb2	GRCm38.p3	14:73183401	AGCCTCTAACATAGT[A/G]CCTTATATATAAAAG	105670
rs30790956	snp	C/T	0.444444	0.157135	intron-variant, utr-variant-5-prime	Rcbtb2	GRCm38.p3	14:73143795	CGCCTGAGTTGAAGC[C/T]AGGCTTCCAGCCGCC	105670
rs30807742	snp	A/T	0.48	0.0979796	intron-variant	Rcbtb2	GRCm38.p3	14:73169452	TCTCCTCAGCTTCTT[A/T]CAGTTTTTCCTAATT	105670
rs30837879	snp	C/G	0.465374	0.126941	intron-variant	Rcbtb2	GRCm38.p3	14:73170017	GGATGGCTTAAGACT[C/G]TAACTATAACAACGC	105670
rs30847105	snp	A/T	0.444444	0.157135	intron-variant	Rcbtb2	GRCm38.p3	14:73143890	CTCCCTTGCACACCC[A/T]GAGATTGCCCTGGCT	105670
rs30871176	snp	C/T	0.5	0	intron-variant	Rcbtb2	GRCm38.p3	14:73145879	GCTCTACTCATCTAA[C/T]CTGAGCTAATGTACA	105670
rs30906434	snp	C/G	0.32	0.24	upstream-variant-2KB, intron-variant	Rcbtb2	GRCm38.p3	14:73141946	TCAGCCTCAGGAACC[C/G]TGAACTTGCTCAAGA	105670
rs30917774	snp	A/T	0.48	0.0979796	intron-variant	Rcbtb2	Mm_Celera	14:73174129	GTCTTTCAGATAAAA[A/T]ATATATCTAGAAACA	105670
rs30922497	snp	A/C/T	0.48	0.0979796	intron-variant	Rcbtb2	GRCm38.p3	14:73180250	AGTGAGCCAGTCTGA[A/C/T]GTGTAGAGAGAAGTG	105670
rs30965758	snp	A/C	0.444444	0.157135	intron-variant	Rcbtb2	Mm_Celera	14:73153528	TAAGCAGGCCTTTAA[A/C]ACTGACTTTTCAAAC	105670
rs30970800	snp	A/G	0.5	0	intron-variant	Rcbtb2	GRCm38.p3	14:73151414	GCTATTTTTTAATAC[A/G]AGACATGATACAATT	105670
rs30973189	snp	C/G	0.444444	0.157135	intron-variant	Rcbtb2	GRCm38.p3	14:73148487	AGAGCGTACTATGGA[C/G]TATGTAAATAAGCCA	105670
rs30993846	snp	A/G	0.444444	0.157135	intron-variant	Rcbtb2	GRCm38.p3	14:73146091	ATAGTTACCTCATCT[A/G]TTAATACCTATTTAA	105670
rs30995700	snp	C/T	0.375	0.216506	intron-variant	Rcbtb2	Mm_Celera	14:73175739	TTCTTTCCTGCCTGC[C/T]TCTTTCCTTCCTAAC	105670
rs31012249	snp	G/T	0.465374	0.126941	intron-variant	Rcbtb2	GRCm38.p3	14:73170340	TAGCTTCCGGGCTCT[G/T]AGCATCCTGCCCAGC	105670
rs31015215	snp	A/G	0.5	0	intron-variant	Rcbtb2	GRCm38.p3	14:73150112	CCAAAGATAAGATAT[A/G]TCCTATGGCTGGCAA	105670
rs31058640	snp	A/C	0.5	0	intron-variant	Rcbtb2	GRCm38.p3	14:73144387	CTGTCACCGTATTGG[A/C]CAATGGCATGCAGGT	105670
rs31210806	snp	C/T	0.5	0	intron-variant	Rcbtb2	GRCm38.p3	14:73154815	CTTCTGATTTTACCA[C/T]GTACTTTTTCCTCAG	105670
rs31222259	snp	C/T	0.375	0.216506	intron-variant	Rcbtb2	GRCm38.p3	14:73147991	ACAACTCCTTAGTAA[C/T]GATTATTTCACTAAC	105670
rs31231837	snp	A/T	0.48	0.0979796	intron-variant	Rcbtb2	Mm_Celera	14:73174132	TTTCAGATAAAAAAT[A/T]TATCTAGAAACAGTC	105670
rs31245062	snp	A/G	0.5	0	intron-variant	Rcbtb2	GRCm38.p3	14:73173412	GCTGGGATTAAAGGC[A/G]TGCGCCACCACGCCC	105670
rs31277074	snp	C/T	0.5	0	intron-variant	Rcbtb2	GRCm38.p3	14:73152339	ACATTAGTAATTTGT[C/T]TTGAGTTATTTTTAA	105670
rs31284098	snp	A/G	0.5	0	intron-variant	Rcbtb2	GRCm38.p3	14:73153924	GACCAGGCTGGCCTC[A/G]AACTCAGAAATCTGC	105670
rs31306286	snp	C/G	0.48	0.0979796	intron-variant	Rcbtb2	GRCm38.p3	14:73153245	AGTGCCATTCTTGAG[C/G]TTGCAAAGAGAGAAG	105670
rs31334663	snp	A/G	0.5	0	intron-variant	Rcbtb2	GRCm38.p3	14:73153357	AGTGCCATAATATAT[A/G]ATGGTGATTAACTAT	105670
rs31338331	snp	C/T	0.5	0	intron-variant	Rcbtb2	Mm_Celera	14:73179647	TCCCCAGCTGTCTTG[C/T]TTATTTTGAGGCAGA	105670
rs31339516	snp	A/G	0.5	0	intron-variant	Rcbtb2	GRCm38.p3	14:73144252	GTTTTGGCGATTAAA[A/G]CCGAGTAAAAGAGAC	105670
rs31371706	snp	C/T	0.444444	0.157135	intron-variant, utr-variant-5-prime	Rcbtb2	GRCm38.p3	14:73143441	CGCGCAGGCCCAGCC[C/T]GGGGTCCGTTTTGTG	105670
rs31387374	snp	A/G	0.32	0.24	intron-variant	Rcbtb2	Mm_Celera	14:73181167	AGTGGTAGTTTCTTA[A/G]GAACATTTGGTTTCC	105670
rs31460023	snp	A/G	0.444444	0.157135	intron-variant	Rcbtb2	Mm_Celera	14:73159755	CCTCCCCTCGTCCCC[A/G]CCACCCCTCCCCCAG	105670
rs31474068	snp	C/G	0.48	0.0979796	intron-variant	Rcbtb2	Mm_Celera	14:73149258	TCATCAAAAGATTTT[C/G]TGTGAGAATTCTCGT	105670
rs31511732	snp	A/G	0.5	0	intron-variant	Rcbtb2	GRCm38.p3	14:73144198	AACGGAGAGGCGAAC[A/G]TGTTTCTCTTTAGAA	105670
rs31529205	snp	A/G	0.375	0.216506	intron-variant	Rcbtb2	GRCm38.p3	14:73148725	AGTTGTCCCAATATG[A/G]ATATCCACGTCTGCT	105670
rs45679238	snp	A/G			intron-variant	Rcbtb2	GRCm38.p3	14:73153127	GTATATGTGTCATAT[A/G]TCCTGGTAGCTCTAG	105670
rs45692261	snp	C/T	0.124444	0.216185	intron-variant	Rcbtb2	Mm_Celera	14:73181302	TTCTGTAGAACTCAA[C/T]CTAAGCGGTGCCACT	105670
rs45761833	snp	A/G			intron-variant	Rcbtb2	GRCm38.p3	14:73162162	AAATTGAAGACATCC[A/G]GGGAAACTAAGGAAT	105670
rs45779713	snp	C/T	0.32	0.24	intron-variant	Rcbtb2	GRCm38.p3	14:73179401	GGAGTGCCCTTTTCC[C/T]TTTTGGTAAACAGTA	105670
rs45791814	snp	C/T			intron-variant	Rcbtb2	GRCm38.p3	14:73157781	TGAAAAGCAATAATA[C/T]ACTCCTATGTCTAGT	105670
rs45834008	snp	A/G			intron-variant	Rcbtb2	GRCm38.p3	14:73144802	GAATTTGGGGGAGGG[A/G]GATTATTATTAACAA	105670
rs45865716	snp	A/C			intron-variant	Rcbtb2	GRCm38.p3	14:73166473	ATCAGTCTTTTCTTT[A/C]CCATAGGTGTTTGCC	105670
rs45896650	snp	A/C	0.32	0.24	upstream-variant-2KB	Rcbtb2	Mm_Celera	14:73137303	GGCTGCTGTAGTTCT[A/C]CTGAGGTCAAGGCCA	105670
rs45923073	snp	C/T			intron-variant	Rcbtb2	GRCm38.p3	14:73157649	ATTAAATATTGTCTC[C/T]AAATAGTATATGCAT	105670
rs45956782	snp	C/T			intron-variant	Rcbtb2	GRCm38.p3	14:73165669	TACAACAAAGACTGT[C/T]TACCAATGAAAGGTC	105670
rs45979166	snp	C/G	0.444444	0.157135	intron-variant	Rcbtb2	Mm_Celera	14:73164180	AGCACACATGTGATT[C/G]ATTCATTCAAAGTGC	105670

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