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
rs6183189	snp	A/G	0.359862	0.224567	intron-variant	Shprh	Mm_Celera	10:11176210	GTATTCCGGGTTTAA[A/G]CACCATGCTATCTAC	268281
rs6196618	snp	C/T	0.359862	0.224567	intron-variant	Shprh	Mm_Celera	10:11176410	TTCTAGAAACATGAA[C/T]CAGATGCTATAATGA	268281
rs6201855	snp	A/G	0.5	0	intron-variant	Shprh	Mm_Celera	10:11170779	GAGGATTCTTCACAT[A/G]TAtttttatgctttc	268281
rs6306783	snp	A/G	0.5	0	utr-variant-5-prime, nc-transcript-variant	Shprh	Mm_Celera	10:11149462	TCCGGCCTGGGTGCC[A/G]GGCTNCACCCAGCGT	268281
rs6306785	snp	C/T	0.5	0	utr-variant-5-prime, nc-transcript-variant	Shprh	Mm_Celera	10:11149467	CCTGGGTGCCNGGCT[C/T]CACCCAGCGTGCAGC	268281
rs6306806	snp	A/G	0.375	0.216506	utr-variant-5-prime, nc-transcript-variant	Shprh	Mm_Celera	10:11149487	CAGCGTGCAGCGCGC[A/G]TGCGCAACTCCCGCA	268281
rs6307290	snp	C/G	0.5	0	utr-variant-5-prime, intron-variant, nc-transcript-variant	Shprh	Mm_Celera	10:11149542	GGGATCTGCAGCCTG[C/G]GAGGAGGGCCGGGCC	268281
rs6307886	snp	C/G	0.5	0	intron-variant	Shprh	Mm_Celera	10:11149690	CGCAGCTCCGGGATC[C/G]GGAGTGATCGGCCCT	268281
rs6316355	snp	A/C	0.304688	0.243945	intron-variant	Shprh	Mm_Celera	10:11195667	TGGAAAGAAGGTAGA[A/C]CTGATCTTGCCAAGA	268281
rs6317901	snp	A/G	0.359862	0.224567	intron-variant	Shprh	Mm_Celera	10:11195980	GAGTTGGAAAGAGGT[A/G]GGTATGTTCAAGGGC	268281
rs29315771	snp	C/T	0.277778	0.248452	intron-variant	Shprh	Mm_Celera	10:11169001	CAGAGTCACTTGATT[C/T]AGCTACATAGCAAGG	268281
rs29317328	snp	A/T	0.48	0.0979796	utr-variant-5-prime, intron-variant, nc-transcript-variant	Shprh	Mm_Celera	10:11149540	CCGGGATCTGCAGCC[A/T]GCGAGGAGGGCCGGG	268281
rs29321281	snp	C/T	0.498615	0.0262793	intron-variant	Shprh	Mm_Celera	10:11184744	ACTTTGGTAATCTCT[C/T]TTTGATCTTAGCAAT	268281
rs29325511	snp	C/T	0.444444	0.157135	intron-variant	Shprh	Mm_Celera	10:11173957	AGGCCAGTGAAAAGA[C/T]GCTGTCTCTAAAAAT	268281
rs29334061	snp	C/T	0.5	0	intron-variant	Shprh	Mm_Celera	10:11200146	CATTGTTCCTGGGTG[C/T]TTGAGAAGCACCCCT	268281
rs29344901	snp	C/T	0.497041	0.0383476	intron-variant	Shprh	Mm_Celera	10:11188861	GTTTTCTCTATCCTG[C/T]GCTCACCATGTGCTC	268281
rs29347773	snp	C/T	0.498615	0.0262793	intron-variant	Shprh	Mm_Celera	10:11193024	ATAGGAAAGCTGCTA[C/T]ATTAATTATTGAGCA	268281
rs29360156	snp	A/T	0.48	0.0979796	intron-variant	Shprh	Mm_Celera	10:11184673	TCTGCTATATTGAAA[A/T]TCTGGGTTTTTTTTT	268281
rs29360946	snp	A/T	0.48	0.0979796	intron-variant	Shprh	GRCm38.p3	10:11201213	TATATGTACATATAT[A/T]TTTTTTTAAAAGATT	268281
rs29362975	snp	C/T	0.48	0.0979796	intron-variant	Shprh	Mm_Celera	10:11180829	TTTAATCAGCTTTAG[C/T]ACAATTACTAGGCCA	268281
rs29375619	snp	A/C	0.456747	0.140554	intron-variant	Shprh	Mm_Celera	10:11165723	GCTGAGCTCAGGTCT[A/C]AAAGCAGCCTCTCAT	268281
rs29377701	snp	C/T	0.444444	0.157135	intron-variant	Shprh	Mm_Celera	10:11199761	ACAGTGACACACTTC[C/T]CCCAGCAAGGCCGCA	268281
rs29381634	snp	A/G	0.375	0.216506	intron-variant	Shprh	Mm_Celera	10:11153494	TGATTTTGAGGACCA[A/G]AATTTTGCTGAGAGC	268281
rs29382487	snp	A/G/T	0.5	0	intron-variant	Shprh	GRCm38.p3	10:11171667	CTCTCTCTCTCTCTC[A/G/T]CACACACACACACAA	268281
rs45632241	snp	C/G	0.32	0.24	intron-variant	Shprh	Mm_Celera	10:11211793	TTTCCAAAGTACAGT[C/G]TAGTGTAAATCAAAA	268281
rs45635074	snp	A/G	0.32	0.24	missense, nc-transcript-variant	Shprh	Mm_Celera	10:11151897	TTAGAGGCCACCGAG[A/G]AAGAGACCCGTTTGT	268281
rs45639792	snp	A/G	0.375	0.216506	intron-variant	Shprh	Mm_Celera	10:11195225	TGAGTAGATTTGAGA[A/G]CAAGTTGAAATTACT	268281
rs45645271	snp	A/T	0.32	0.24	intron-variant	Shprh	Mm_Celera	10:11174343	TTCAGAGCACAGCAT[A/T]GAGTAGCCCTTGCTT	268281
rs45666735	snp	C/T	0.32	0.24	intron-variant	Shprh	Mm_Celera	10:11202482	CTTTTAATAAGGGAC[C/T]TTAGCAGCCAGGAGC	268281
rs45684409	snp	C/G	0.32	0.24	intron-variant	Shprh	Mm_Celera	10:11162382	TTTAACACAGAGCAT[C/G]GTTACAAGTTACATC	268281
rs45705291	snp	A/G	0.408163	0.193609	intron-variant	Shprh	Mm_Celera	10:11183355	CTCTCTCCAGGGGCC[A/G]TCACATTGAGCTTAG	268281
rs45716037	snp	C/T	0.32	0.24	intron-variant	Shprh	Mm_Celera	10:11177061	GTTTTGAGATTTTCT[C/T]CAGAGAGCAAGAGTA	268281
rs45750866	snp	A/C	0.231111	0.249285	intron-variant	Shprh	Mm_Celera	10:11189846	ACATAAAGCCAAAGC[A/C]GCGATGTCTTCTAGT	268281
rs45760409	snp	A/G			utr-variant-3-prime, nc-transcript-variant	Shprh	Mm_Celera	10:11215038	TACTGTTCTTCCACC[A/G]AGTTGTGTGCCATGC	268281
rs45788157	snp	C/T	0.132653	0.220748	intron-variant	Shprh	Mm_Celera	10:11189868	TCTTCTAGTAATAGT[C/T]ACTGTCATAAAAATG	268281
rs45789803	snp	A/G	0.260355	0.249785	intron-variant	Shprh	Mm_Celera	10:11161003	AAGTAGAACTTAGTG[A/G]TTGACTGATAGCTTA	268281
rs45802985	snp	A/T	0.142012	0.225474	intron-variant	Shprh	Mm_Celera	10:11164197	GGGTAAATTAGAATA[A/T]GTTTATCATGAACAA	268281
rs45820865	snp	A/G	0.132653	0.220748	intron-variant	Shprh	Mm_Celera	10:11149903	TGCAGAGGCCGCCAA[A/G]TTAGGCTGGCAAACT	268281
rs45834237	snp	C/T	0.152778	0.230321	intron-variant	Shprh	Mm_Celera	10:11157352	GAAAGGAGAATAATT[C/T]TCTGTCTTTCAGAAT	268281
rs45838209	snp	C/T	0.124444	0.216185	intron-variant	Shprh	Mm_Celera	10:11173598	GCTAATGAGTCTAAA[C/T]TTGCTTCAAGGTGTG	268281
rs45843741	snp	C/T	0.336735	0.234472	intron-variant	Shprh	Mm_Celera	10:11197120	GATCTGAGGATAATG[C/T]AGTCTGTCTCTGAAT	268281
rs45881562	snp	A/G			intron-variant	Shprh	Mm_Celera	10:11151383	GTGCACATTAGGGCT[A/G]TAAGCCTGAATATTG	268281
rs45890110	snp	A/G	0.142012	0.225474	intron-variant, missense, utr-variant-3-prime	Shprh	Mm_Celera	10:11207874	TACACAAGCACACAT[A/G]ACCACACACTAAGTA	268281
rs45945427	snp	A/G	0.124444	0.216185	intron-variant	Shprh	Mm_Celera	10:11158123	GATAATTTCTTCCAA[A/G]TATTCTAGCAACCTA	268281
rs45945809	snp	A/C/T	0.297521	0.245442	intron-variant	Shprh	GRCm38.p3	10:11160380	TTTCAGTAAACTTAA[A/C/T]GTTGCATTCATTTCT	268281
rs45975236	snp	A/G	0.391111	0.206368	utr-variant-3-prime, nc-transcript-variant	Shprh	Mm_Celera	10:11216070	ATGATTGAATTGTCT[A/G]TTCATTAAACTTGGA	268281
rs45991124	snp	C/T	0.32	0.24	intron-variant	Shprh	Mm_Celera	10:11165902	TTTGCCATTGGGCAG[C/T]TCTTTTTAGTCTTAG	268281
rs45995942	snp	A/G	0.32	0.24	intron-variant	Shprh	Mm_Celera	10:11213293	TTCAGAATTATTTAG[A/G]CATTTTCACTGATTT	268281
rs46023263	snp	A/G	0.124444	0.216185	intron-variant	Shprh	Mm_Celera	10:11180550	GGTTGATAATCCCTA[A/G]TCTTATTTTCCTATG	268281
rs46043403	snp	G/T	0.124444	0.216185	intron-variant	Shprh	Mm_Celera	10:11174113	GCTTGTTCAGAGACA[G/T]ATGTAGTTTCTGTAG	268281
rs46043932	snp	C/T	0.32	0.24	intron-variant	Shprh	Mm_Celera	10:11180338	ATAAAGAGGTTTTTC[C/T]CTTCCTCTGATCTCT	268281
rs46045552	snp	A/G	0.32	0.24	intron-variant	Shprh	Mm_Celera	10:11190925	ATTCAGAAAAATCAT[A/G]CATGTTTAACATAGT	268281
rs46069765	snp	C/G	0.231111	0.249285	intron-variant	Shprh	Mm_Celera	10:11177132	CTGCCGGTGTCACCA[C/G]CCTTCTTTATAGTAA	268281
rs46077390	snp	C/T	0.231111	0.249285	intron-variant	Shprh	Mm_Celera	10:11193152	TGTGTGCCTATCATG[C/T]AGTTAGCCCTGGGTC	268281
rs46085656	snp	C/T	0.336735	0.234472	intron-variant	Shprh	Mm_Celera	10:11204267	CCATTTAGGTCATGG[C/T]AGTGTTCATGTTTAA	268281
rs46096591	snp	C/T	0.244898	0.249948	synonymous-codon, nc-transcript-variant	Shprh	Mm_Celera	10:11160599	AGACGTCAAGCAGGA[C/T]GCTCTCACCCTTCCT	268281
rs46098569	snp	C/T	0.124444	0.216185	intron-variant	Shprh	Mm_Celera	10:11152608	ACTTAATTTCCTGAT[C/T]GTAAAACTTAAGTGT	268281
rs46124175	snp	A/G	0.152778	0.230321	intron-variant	Shprh	Mm_Celera	10:11159761	TTCTCAGTGAATACA[A/G]TTATAATAGACTGTA	268281
rs46172754	snp	A/T	0.231111	0.249285	intron-variant	Shprh	Mm_Celera	10:11185075	TAAAACAGCTTTGAA[A/T]CACAAATTTTACATA	268281
rs46186040	snp	A/G	0.124444	0.216185	intron-variant	Shprh	Mm_Celera	10:11210743	TGGGCAAGAGGATAC[A/G]GGACCTAACACTGAT	268281
rs46205837	snp	C/G	0.124444	0.216185	upstream-variant-2KB	Shprh	Mm_Celera	10:11148762	CACAGAAAAAAATTC[C/G]AAGGACATACAAAGC	268281
rs46223372	snp	A/G	0.231111	0.249285	intron-variant	Shprh	Mm_Celera	10:11174094	TGTACAACAACAGAA[A/G]ACTGCTTGTTCAGAG	268281
rs46229754	snp	G/T	0.46281	0.131194	intron-variant	Shprh	Mm_Celera	10:11158870	CAGTACTTGATTGTG[G/T]AATTATTGAGTTGTA	268281
rs46297506	snp	C/T	0.32	0.24	intron-variant	Shprh	Mm_Celera	10:11205309	TTCAGTCTAGCTGGT[C/T]TTCCACCTCTACTTA	268281
rs46298181	snp	A/G	0.124444	0.216185	intron-variant	Shprh	Mm_Celera	10:11177552	CTCTTAAGTACAAAC[A/G]GGAAACTGCGTAAGC	268281
rs46299623	snp	C/T	0.336735	0.234472	synonymous-codon, nc-transcript-variant	Shprh	Mm_Celera	10:11164962	GGTGGATGAAATCAA[C/T]CGGCACGTGAGGTCA	268281
rs46334869	snp	A/G	0.124444	0.216185	intron-variant	Shprh	Mm_Celera	10:11169511	TAAGAGTGGTGATTC[A/G]CTAAGTTTTGTGTGT	268281
rs46353451	snp	A/T	0.35503	0.226867	intron-variant	Shprh	Mm_Celera	10:11187367	TTGAAGTTCTTGTTA[A/T]TTTCTTCATCAGAAA	268281
rs46370095	snp	A/G			intron-variant	Shprh	Mm_Celera	10:11204811	TGCGTGACATGGCAC[A/G]TGTGCAGAGTCAGGG	268281
rs46448666	snp	G/T			intron-variant	Shprh	Mm_Celera	10:11161873	CCCAGTTGCATATGA[G/T]TATATGCTTTTTTTT	268281
rs46458963	snp	A/G	0.231111	0.249285	intron-variant	Shprh	Mm_Celera	10:11192127	TTCTGTGTCACCATA[A/G]CAGTTAGTAATTTGT	268281
rs46462118	snp	A/G	0.48	0.0979796	upstream-variant-2KB, nc-transcript-variant	Shprh	Mm_Celera	10:11149356	CTTTTTGAAGCCAAC[A/G]CCGGAAAGAGGGGCG	268281
rs46526047	snp	A/C	0.142012	0.225474	intron-variant	Shprh	Mm_Celera	10:11167334	TTATTTATCTTTATA[A/C]TATCTCCAGTGACCA	268281
rs46557651	snp	C/T	0.231111	0.249285	intron-variant	Shprh	Mm_Celera	10:11180598	CCAGCTGCACTCACT[C/T]CCAAGTTACTTGCTA	268281
rs46563169	snp	A/G	0.32	0.24	intron-variant	Shprh	Mm_Celera	10:11162520	GATGGATTTTCTTAG[A/G]AATCGTAGCATAACA	268281
rs46590264	snp	C/T	0.244898	0.249948	upstream-variant-2KB	Shprh	Mm_Celera	10:11147986	TTGATATTCTTTTCA[C/T]GGCCATGGAGCAAGG	268281
rs46610258	snp	A/G	0.336735	0.234472	intron-variant	Shprh	Mm_Celera	10:11183320	CTAAGGCCTCCATTC[A/G]CCTCAGTTAGCTTGC	268281
rs46646203	snp	A/G	0.231111	0.249285	intron-variant	Shprh	Mm_Celera	10:11174222	GTGTCTTCCTTTGCA[A/G]GATGCTTGAGGAGCA	268281
rs46675435	snp	C/T	0.231111	0.249285	upstream-variant-2KB	Shprh	Mm_Celera	10:11148220	CGTTTCTATAGGTGC[C/T]TCCTCTTCTGCCAGC	268281
rs46685491	snp	A/T	0.124444	0.216185	intron-variant	Shprh	Mm_Celera	10:11179379	TTTTCAGGCTTTAGA[A/T]CTTAACATCGCCATG	268281
rs46687202	snp	A/C/G			intron-variant	Shprh	GRCm38.p3	10:11213084	GCTTTTCATCTAAAC[A/C/G]TGAAAGATGTTTGTT	268281
rs46715076	snp	C/T	0.32	0.24	intron-variant	Shprh	Mm_Celera	10:11194448	TTGGCACAGTGAGCG[C/T]AGAAACCACTGTTGA	268281
rs46719142	snp	A/C	0.32	0.24	intron-variant, utr-variant-3-prime	Shprh	Mm_Celera	10:11208196	AGTTTGGAACTGCTG[A/C]GGTAAAACATGAGAA	268281
rs46725059	snp	C/G	0.142012	0.225474	intron-variant	Shprh	Mm_Celera	10:11181367	ATGTCCATTTTCCTT[C/G]GTGGTGGTGGGGCAA	268281
rs46740274	snp	A/G	0.124444	0.216185	intron-variant	Shprh	Mm_Celera	10:11178284	TTCTTTATTACTGTC[A/G]ATGACCAAAATTTGT	268281
rs46742745	snp	A/G	0.32	0.24	intron-variant	Shprh	Mm_Celera	10:11180662	AGTCTGTCTTCAGGG[A/G]CACTTCTTTTGGCCC	268281
rs46759597	snp	A/C	0.489796	0.070696	intron-variant	Shprh	Mm_Celera	10:11182180	AAATGGATTTGATAA[A/C]TATATTTAACCCTTT	268281
rs46778160	snp	A/G	0.336735	0.234472	intron-variant	Shprh	Mm_Celera	10:11163974	TGTGTACCGATGGCA[A/G]CAAATAGTAATCACC	268281
rs46789688	snp	C/G	0.142012	0.225474	intron-variant	Shprh	Mm_Celera	10:11193542	CAACTGGAACAAAAT[C/G]AACTTTCCTCATAAA	268281
rs46853254	snp	C/T	0.231111	0.249285	intron-variant	Shprh	Mm_Celera	10:11193243	TTAGAGATGCTGCCA[C/T]TTGTTCTCAGAGTCT	268281
rs46894823	snp	A/G	0.375	0.216506	intron-variant	Shprh	Mm_Celera	10:11199296	ATTCTGATTGTCAGA[A/G]AAGAAAGTTTCTATT	268281
rs46925573	snp	C/G	0.277778	0.248452	intron-variant	Shprh	Mm_Celera	10:11160845	AGGGAATATACAGTA[C/G]TAAGTTTATCAGTCT	268281
rs46934191	snp	G/T	0.32	0.24	intron-variant	Shprh	Mm_Celera	10:11174672	CATTTTGGTAAGTGT[G/T]CTCTGTAGTAGTAGT	268281
rs46935162	snp	A/T	0.260355	0.249785	intron-variant	Shprh	Mm_Celera	10:11159612	GTAAGGCAAAATCTT[A/T]TATGTCTGATTTTTA	268281
rs46936053	snp	G/T	0.277778	0.248452	intron-variant	Shprh	Mm_Celera	10:11156663	GTATAAAATAACACA[G/T]GAGCACTGAGCAGAA	268281
rs46941547	snp	A/C	0.32	0.24	intron-variant	Shprh	Mm_Celera	10:11212887	TTCCTTCAAAGTCAT[A/C]TTGAAATAAACCAGT	268281
rs46955728	snp	C/T	0.231111	0.249285	synonymous-codon, nc-transcript-variant	Shprh	Mm_Celera	10:11192539	TTGTCCAATCTGTGC[C/T]CGACAGCTGGGAAAA	268281
rs46987203	snp	C/T	0.132653	0.220748	intron-variant	Shprh	Mm_Celera	10:11191685	TTAAAGGTTGTCTAC[C/T]TTGCTGACTATCTGA	268281
rs46990775	snp	C/T	0.32	0.24	intron-variant	Shprh	Mm_Celera	10:11212072	CTCCTGTGCTTAGTG[C/T]CTAATGCCCTTCTCT	268281
rs47053310	snp	A/C	0.124444	0.216185	intron-variant	Shprh	Mm_Celera	10:11154017	GTCTGTTTTTTTCCA[A/C]TTTTACTTCCTATGA	268281

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