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
rs4229089	snp	A/C	0.21875	0.248039	nc-transcript-variant	Klhl11	GRCm38.p3	11:100457823	CCTTGAACTAAACTT[A/C]TGTGCAAAGGCCATA	217194
rs4229090	snp	C/T	0.21875	0.248039	nc-transcript-variant	Klhl11	GRCm38.p3	11:100457802	AAAGGCCATATTAGT[C/T]ACGTTTCGTGTCTTT	217194
rs4229091	snp	A/C	0.21875	0.248039	nc-transcript-variant	Klhl11	GRCm38.p3	11:100457679	TCTTAGCCGTCAAAC[A/C]TTTTGGCACAGCTCA	217194
rs4229092	snp	C/T	0.21875	0.248039	nc-transcript-variant	Klhl11	GRCm38.p3	11:100457555	AATACAACAATAGTA[C/T]GTTTACAAAGTG	217194
rs13468827	snp	A/G	0.32	0.24	nc-transcript-variant	Klhl11	GRCm38.p3	11:100458053	GGACCAAAAATTTAA[A/G]ACTCTCAGTCTAAAA	217194
rs13468828	snp	A/T			nc-transcript-variant	Klhl11	Mm_Celera	11:100457767	ATGTATGGTGTTGTG[A/T]AACGAATATTCTTCT	217194
rs13468829	snp	G/T			nc-transcript-variant	Klhl11	Mm_Celera	11:100457609	TTACTTACAGCATAT[G/T]TTCTGGTGATTGAAA	217194
rs27058899	snp	A/G	0.231111	0.249285	upstream-variant-2KB	Klhl11	Mm_Celera	11:100474541	AAAATGGATGTTGCC[A/G]ACCTTGGAAGAACAC	217194
rs27058900	snp	A/G	0.336735	0.234472	utr-variant-5-prime, nc-transcript-variant	Klhl11	Mm_Celera	11:100472781	GGTGCGGCAAGTCTG[A/G]TGCGACACAGAGGCA	217194
rs27058901	snp	A/G	0.336735	0.234472	synonymous-codon, nc-transcript-variant	Klhl11	GRCm38.p3	11:100472615	ACTGCCTCGGACCTC[A/G]GCGGCCAGGCTCGCG	217194
rs27058902	snp	A/C	0.244898	0.249948	intron-variant	Klhl11	Mm_Celera	11:100472041	CTCAGGGGTGCAATG[A/C]GCACAAGCTAGACTC	217194
rs27058903	snp	A/G	0.336735	0.234472	intron-variant	Klhl11	Mm_Celera	11:100471897	CTCTTGCCACTGCGA[A/G]GCTGGTTTAAATGAC	217194
rs27058904	snp	C/T	0.336735	0.234472	intron-variant	Klhl11	Mm_Celera	11:100471827	AGCCTGGACCCTGAC[C/T]GAGGCCTTTGGGAAG	217194
rs27058905	snp	C/T	0.152778	0.230321	intron-variant	Klhl11	Mm_Celera	11:100471588	CAACCTCTGTGGCGT[C/T]CTTTCTGGCTCCCCA	217194
rs27058906	snp	C/T	0.244898	0.249948	intron-variant	Klhl11	Mm_Celera	11:100468649	CTCAATTCACTCTGC[C/T]GGATTCTTTAATGCT	217194
rs27058907	snp	C/T	0.132653	0.220748	intron-variant	Klhl11	Mm_Celera	11:100468604	TTTGACAGTAGACTC[C/T]ACCCCCTTTTTAGGC	217194
rs27058908	snp	A/T	0.244898	0.249948	intron-variant	Klhl11	Mm_Celera	11:100468392	GATCTACCTTGATTT[A/T]AAAACCTCCTGTGTC	217194
rs27058909	snp	G/T	0.408163	0.193609	intron-variant	Klhl11	Mm_Celera	11:100468035	CTGAGGATCCAGTCT[G/T]GTACTCTGAGAAAAG	217194
rs27058910	snp	A/G	0.35503	0.226867	intron-variant	Klhl11	Mm_Celera	11:100467854	CACCACCACTGTACA[A/G]CACAGTTAGCTTTAA	217194
rs27058911	snp	A/G	0.132653	0.220748	intron-variant	Klhl11	Mm_Celera	11:100466281	CCATCATTCATCATG[A/G]CAGGCCCATTTCCAT	217194
rs27058912	snp	C/T	0.32	0.24	intron-variant	Klhl11	Mm_Celera	11:100466165	TTGGTAGTACTTAGC[C/T]CAAGGGTGGTCAATT	217194
rs27058913	snp	C/T	0.32	0.24	utr-variant-3-prime, nc-transcript-variant	Klhl11	GRCm38.p3	11:100462859	AGCTGCAAACGCTGG[C/T]GAGCTCAGCATTCAA	217194
rs27058914	snp	A/G	0.336735	0.234472	utr-variant-3-prime, intron-variant	Klhl11	GRCm38.p3	11:100462647	AATAAGATCTTATTT[A/G]CCAGCACACAAACAC	217194
rs27058915	snp	C/T	0.124444	0.216185	downstream-variant-500B, intron-variant	Klhl11	Mm_Celera	11:100462223	CTTCCCAACTATCAT[C/T]TCAGGATGATGGCTT	217194
rs27058916	snp	C/T	0.231111	0.249285	intron-variant	Klhl11	Mm_Celera	11:100462066	CTGTGTTGATTGTCA[C/T]GGCACACTGCATCCT	217194
rs27058917	snp	A/G/T	0.391111	0.206368	intron-variant	Klhl11	GRCm38.p3	11:100462037	AGCGGAGCAAAAAAC[A/G/T]AACTGAAGGCATCCT	217194
rs27058918	snp	C/G	0.32	0.24	intron-variant	Klhl11	Mm_Celera	11:100461402	AAAGATATTCCTAAT[C/G]CAACTGAAAAATTAA	217194
rs27058919	snp	C/T	0.124444	0.216185	intron-variant	Klhl11	Mm_Celera	11:100461384	TAAGAGAGAATGGGG[C/T]GCAAAGATATTCCTA	217194
rs27058920	snp	A/C	0.124444	0.216185	intron-variant	Klhl11	Mm_Celera	11:100461350	CTCCAATGCCATATG[A/C]AACAAAGAATGCAGA	217194
rs27058921	snp	C/G	0.231111	0.249285	intron-variant	Klhl11	Mm_Celera	11:100461122	GATTACCCACAAAAG[C/G]TTAAGGGTGAGAGTG	217194
rs27058922	snp	G/T	0.124444	0.216185	intron-variant	Klhl11	Mm_Celera	11:100460180	AAAAGGGAGTGTGCC[G/T]CTATGCCACTGGAAC	217194
rs27058923	snp	A/G	0.124444	0.216185	intron-variant	Klhl11	Mm_Celera	11:100459953	CTTGAATGCTAACTT[A/G]CATAAAAAGCTCAGG	217194
rs27058924	snp	C/T	0.124444	0.216185	intron-variant	Klhl11	Mm_Celera	11:100459918	AGTCTTCTCTCTACA[C/T]CGAGTGTTGAAAGAT	217194
rs27058925	snp	C/T	0.124444	0.216185	intron-variant	Klhl11	Mm_Celera	11:100459371	GTTATAGTAAACAGC[C/T]AAAGTTTCTGGTTGT	217194
rs27058926	snp	C/T	0.231111	0.249285	intron-variant	Klhl11	Mm_Celera	11:100459015	AGTGCCTCTTAGGAT[C/T]CAGAGACTTGTAATG	217194
rs27058927	snp	C/G	0.124444	0.216185	intron-variant	Klhl11	Mm_Celera	11:100458919	TGAGATCCTAAATGA[C/G]TTGTGGACTGAGAGA	217194
rs27058928	snp	G/T	0.124444	0.216185	nc-transcript-variant	Klhl11	Mm_Celera	11:100458175	ACAGAAAAGCAAAGC[G/T]CTCAGGATACACAAG	217194
rs27058929	snp	A/C	0.124444	0.216185	nc-transcript-variant	Klhl11	Mm_Celera	11:100457994	CACAAGAACCTGTCT[A/C]CTAGTTGTGACAGGA	217194
rs27058930	snp	A/G	0.231111	0.249285	nc-transcript-variant	Klhl11	GRCm38.p3	11:100457758	TTCTAGTGTAGAAGA[A/G]TATTCGTTTCACAAC	217194
rs27058931	snp	A/G	0.124444	0.216185	downstream-variant-500B, nc-transcript-variant	Klhl10, Klhl11	Mm_Celera	11:100457480	GGTCAGAGAGTAAGC[A/G]GGAAGCTCTGAGGGT	217194
rs27058932	snp	C/T	0.124444	0.216185	downstream-variant-500B, nc-transcript-variant	Klhl10, Klhl11	Mm_Celera	11:100457450	GGTGCTTCAAGGTCC[C/T]GCCCTCCTAGCAAGG	217194
rs27058933	snp	C/T	0.5	0	downstream-variant-500B, nc-transcript-variant	Klhl10, Klhl11	Mm_Celera	11:100457231	GTGTTCTAAATACTA[C/T]ATCTCCTCTAACATA	217194
rs27058934	snp	C/T	0.124444	0.216185	downstream-variant-500B	Klhl10, Klhl11	Mm_Celera	11:100457101	GAAGGGGATTACATT[C/T]AACACACAGTACAAA	217194
rs27058935	snp	C/T	0.375	0.216506	synonymous-codon, downstream-variant-500B	Klhl10, Klhl11	Mm_Celera	11:100456697	GATCGAGGTAGTGGA[C/T]GACCTCTTGTTTGTG	217194
rs29440535	snp	C/G	0.375	0.216506	intron-variant	Klhl11	Mm_Celera	11:100467195	AGGTAGCTGGGATTA[C/G]AATGCTGAGCCAAGA	217194
rs45743962	snp	C/T			intron-variant	Klhl11	Mm_Celera	11:100467812	TCTGCCTGCCTCTGC[C/T]TCCCAAGTGTTGGGA	217194
rs211823040	snp	C/G			intron-variant	Klhl11	Mm_Celera	11:100470739	GCACCCTGTCCTGCC[C/G]TTTTTTTGACATGGA	217194
rs211856277	in-del	-/AT			intron-variant	Klhl11	Mm_Celera	11:100466064	GGGTCAAGTGGTTTG[-/AT]ATGTTACTAATAGAA	217194
rs212028420	in-del	-/TTG			intron-variant	Klhl11	Mm_Celera	11:100465387	ATCCCTTTGCAGCCA[-/TTG]TTGGAACCTTTTATT	217194
rs212292460	snp	C/T			upstream-variant-2KB	Klhl11	Mm_Celera	11:100474378	ACTTTGAGTCTTAGG[C/T]TGGTAAAAGTAGCAC	217194
rs212366502	snp	A/G			intron-variant	Klhl11	Mm_Celera	11:100469242	ACATCCCTATTCTAA[A/G]ACTATGTTTTAGTGT	217194
rs212844533	in-del	-/TTAC			upstream-variant-2KB	Klhl11	Mm_Celera	11:100474505	GGTGAAGGTGAGGAA[-/TTAC]TTATGTCTGATTTCC	217194
rs213017967	snp	C/T			intron-variant	Klhl11	Mm_Celera	11:100471983	GAGTCGAACACGACC[C/T]ACCGTTTTTCATCGC	217194
rs213104042	snp	C/G			intron-variant	Klhl11	Mm_Celera	11:100459207	CTTTCTGTGGAAAGG[C/G]ACTTGCAGTTTCCCA	217194
rs213139894	snp	C/T			upstream-variant-2KB	Klhl11	Mm_Celera	11:100474411	ACCTGTAACTCCAGC[C/T]GTTGGGACGCTAAGG	217194
rs213183940	snp	A/G			intron-variant	Klhl11	Mm_Celera	11:100461546	CTGGAGGGAGTAGAA[A/G]CAGCTGCTGCTGAAA	217194
rs213429888	snp	A/G			upstream-variant-2KB	Klhl11	Mm_Celera	11:100472988	TTATGTTGCTTTGGA[A/G]TGTATCCTCGCCATC	217194
rs213461598	in-del	-/TG			upstream-variant-2KB	Klhl11	Mm_Celera	11:100473037	GTTTGTTTGTTTGTT[-/TG]TTTTAACTTTGTAGA	217194
rs213724944	in-del	-/A			intron-variant	Klhl11	Mm_Celera	11:100461416	TCCAACTGAAAAATT[-/A]AAAGATCATGAACAT	217194
rs213898167	snp	C/T			upstream-variant-2KB	Klhl11	Mm_Celera	11:100472917	TCAGGTCTACCTTTT[C/T]TCGCCCCTCCATTAT	217194
rs214140669	snp	G/T			upstream-variant-2KB	Klhl11	Mm_Celera	11:100474592	TGAATTTCAGAACAG[G/T]CTAGTCTAGTGAGTT	217194
rs214316791	snp	C/T			intron-variant	Klhl11	Mm_Celera	11:100466176	TAGCTCAAGGGTGGT[C/T]AATTTGAGACCATGG	217194
rs214503763	snp	G/T			intron-variant	Klhl11	Mm_Celera	11:100459901	CCAGTACCTAAAACA[G/T]AAGTCTTCTCTCTAC	217194
rs214719303	in-del	-/AAAT			intron-variant	Klhl11	Mm_Celera	11:100470396	TCTCCGAAAAAAAAA[-/AAAT]TTTTTTTTCCTTACT	217194
rs214754247	in-del	-/G			intron-variant	Klhl11	Mm_Celera	11:100464797	ACCCTATATATCATA[-/G]ACACACAGTAATACA	217194
rs215056242	snp	A/G			intron-variant	Klhl11	Mm_Celera	11:100464772	CTTACCTCCAGATGT[A/G]CACTGTGGTACCCTA	217194
rs215116013	snp	C/T			intron-variant	Klhl11	Mm_Celera	11:100465933	GTTCTATATCTTATT[C/T]GGAAGGTAGCCAGGA	217194
rs215250243	snp	A/G			upstream-variant-2KB	Klhl11	Mm_Celera	11:100474504	GGGTGAAGGTGAGGA[A/G]TTACTTATGTCTGAT	217194
rs215282249	snp	A/G			upstream-variant-2KB	Klhl11	Mm_Celera	11:100473367	ATAAGGGTGTTGGGA[A/G]CCAACAATCAAACTG	217194
rs215599392	snp	C/T			intron-variant	Klhl11	Mm_Celera	11:100469058	GATTGAAGGTGTATG[C/T]TGAGCCTCCACTGCC	217194
rs215628356	snp	C/T			intron-variant	Klhl11	Mm_Celera	11:100468158	TGGTTTTGAGACAGT[C/T]AAGACTCCATGTAGT	217194
rs217504372	snp	C/T			intron-variant	Klhl11	Mm_Celera	11:100471116	CCTGCCTCCTTCATG[C/T]AGCTATATAACCCAC	217194
rs217621505	snp	C/T			intron-variant	Klhl11	Mm_Celera	11:100468013	CTTATACCCATTCCA[C/T]CCAATCCTGAGGATC	217194
rs218003182	snp	G/T			intron-variant	Klhl11	Mm_Celera	11:100468881	AATCAGAGATCCAAC[G/T]GACCCTGCCTCCTAA	217194
rs218027099	in-del	-/AGA			intron-variant	Klhl11	Mm_Celera	11:100467932	TAACTCTGAAAAAAG[-/AGA]AAAAAAAAAATCACA	217194
rs218189691	snp	A/G			intron-variant	Klhl11	Mm_Celera	11:100464584	GACTACCCTCCCTCT[A/G]CAAATTAGCAAACAG	217194
rs218467767	in-del	-/AC			intron-variant	Klhl11	Mm_Celera	11:100470591	ATACTATACATATAT[-/AC]ACACAGGTAAAACAC	217194
rs218511862	in-del	-/AAC			intron-variant	Klhl11	Mm_Celera	11:100458807	AAAGATGGCTCTAAT[-/AAC]AACTTAATGGTGACT	217194
rs218689577	in-del	-/TTTTTTT			intron-variant	Klhl11	GRCm38.p3	11:100465411	TTTTATTTATTTGCC[-/TTTTTTT]TTTTTTTTTTTTGAG	217194
rs218770807	in-del	-/T			intron-variant	Klhl11	Mm_Celera	11:100470395	GTCTCCGAAAAAAAA[-/T]ATTTTTTTTCCTTAC	217194
rs219386696	in-del	-/TATT			upstream-variant-2KB	Klhl11	Mm_Celera	11:100474189	GCCCATAAAACAGAA[-/TATT]TGTTTGTTTGTCTGT	217194
rs219496467	snp	G/T			intron-variant	Klhl11	Mm_Celera	11:100471211	GAACATTCTTTATGT[G/T]CCCAATTTAAAAATA	217194
rs219526224	snp	A/G			intron-variant	Klhl11	Mm_Celera	11:100469780	GAAATAGTAGGTACA[A/G]ATAGTTGTGAGCCAC	217194
rs219556736	snp	G/T			downstream-variant-500B	Klhl10, Klhl11	Mm_Celera	11:100457091	AGGGAGTAAGGAAGG[G/T]GATTACATTCAACAC	217194
rs219848342	snp	A/C			intron-variant	Klhl11	Mm_Celera	11:100464832	CAGGCATGCGCCTCT[A/C]ATGCTAATACTCAGG	217194
rs219878781	snp	C/T			intron-variant	Klhl11	Mm_Celera	11:100462090	GCATCCTCATCAACA[C/T]AACCATTCAAAGTGT	217194
rs220357088	snp	C/G			intron-variant	Klhl11	Mm_Celera	11:100469877	GGGCTGTCAGTCCAG[C/G]CCCCCACCTTATTTT	217194
rs220520039	snp	A/C			intron-variant	Klhl11	Mm_Celera	11:100460510	TCTCAGAGCCAATCC[A/C]GCATTAACAGTGTTT	217194
rs220560576	snp	C/T			intron-variant	Klhl11	Mm_Celera	11:100468243	TAAAGGCAAGAGCCA[C/T]CACAGCCCAGAGTCA	217194
rs220665757	snp	A/G			intron-variant	Klhl11	Mm_Celera	11:100461879	TAAGTTCCAGTAGAA[A/G]TCTAGGGCAACTAGG	217194
rs220703434	in-del	-/C			downstream-variant-500B	Klhl10, Klhl11	Mm_Celera	11:100457033	AAACTTGTAAGAGTA[-/C]TGGAAAATGTTCAAC	217194
rs220755298	snp	A/G			upstream-variant-2KB	Klhl11	Mm_Celera	11:100473994	AACCAGGGCAGTTTA[A/G]TCACCCCAGCACCAA	217194
rs220838180	snp	C/T			intron-variant	Klhl11	Mm_Celera	11:100467024	GTCTCTTCATAACAA[C/T]AGAAACCCTAAGACA	217194
rs220956283	snp	A/G			nc-transcript-variant	Klhl11	Mm_Celera	11:100458704	CCCTTCATTCAGCCA[A/G]GGCCTAGGCTGCCTG	217194
rs221240529	snp	C/T			intron-variant	Klhl11	Mm_Celera	11:100471258	TCTATAGATTGAGTT[C/T]CAGGACAACCAGCAT	217194
rs221311547	snp	C/T			intron-variant	Klhl11	Mm_Celera	11:100459983	GAGTGTATATAAAGT[C/T]AGAAAAATGGCTATT	217194
rs221359459	snp	C/G			upstream-variant-2KB	Klhl11	Mm_Celera	11:100474673	GTTGGGCATGGTGGC[C/G]CACGCCTTTAATCCC	217194
rs221396743	in-del	-/TCAAGTTAGGAG			intron-variant	Klhl11	Mm_Celera	11:100458746	AGACAGTGGTTTCAA[-/TCAAGTTAGGAG]TCATACTGTCTGCCA	217194
rs222011388	snp	C/T			synonymous-codon, nc-transcript-variant	Klhl11	Mm_Celera	11:100472276	TTCCACCGTGTCAGG[C/T]TCGGGTCCGGGCTCT	217194
rs222194452	snp	G/T			intron-variant	Klhl11	Mm_Celera	11:100466778	AGGTGGGCTCTGAGG[G/T]CCTGTGCTCAGATTT	217194

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