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
rs26941016	snp	A/G	0.444444	0.157135	downstream-variant-500B, upstream-variant-2KB	Fbxw10, Tvp23b	Mm_Celera	11:62877870	AAGAAAATACGCTTC[A/G]TTTTCTACAAAGGAG	213980
rs26941017	snp	C/T	0.42	0.183303	downstream-variant-500B, upstream-variant-2KB	Fbxw10, Tvp23b	GRCm38.p3	11:62877738	TATTTTTGCAAAGAC[C/T]AAAACTCAGTTTTGG	213980
rs26941018	snp	A/T	0.408163	0.193609	downstream-variant-500B, upstream-variant-2KB	Fbxw10, Tvp23b	GRCm38.p3	11:62877629	AAGGTCACTGAGCAG[A/T]TAGACTCCATTCATC	213980
rs26941019	snp	G/T	0.497041	0.0383476	synonymous-codon, nc-transcript-variant, downstream-variant-500B	Fbxw10	GRCm38.p3	11:62876868	CGCAGTTGATCAGCT[G/T]CGATCCAGCAATCTT	213980
rs26941020	snp	A/G	0.336735	0.234472	missense, nc-transcript-variant, downstream-variant-500B	Fbxw10	Mm_Celera	11:62876845	CTCAAAGGAAAATCA[A/G]TTCAACACGCAGTTG	213980
rs26941021	snp	C/T	0.124444	0.216185	synonymous-codon, nc-transcript-variant	Fbxw10	Mm_Celera	11:62876703	GACACCTGACCGATT[C/T]CTTCTGACTATCAGT	213980
rs26941022	snp	A/G	0.49827	0.0293608	intron-variant	Fbxw10	GRCm38.p3	11:62875373	ACTTCTGAGAGAGAA[A/G]ATGTGCACCTGAAAA	213980
rs26941023	snp	A/C	0.21875	0.248039	intron-variant, nc-transcript-variant	Fbxw10	GRCm38.p3	11:62874793	TTCCTGGGGCCACTG[A/C]CTTGCCACAGCTCCC	213980
rs26941024	snp	A/G	0.495868	0.0452663	intron-variant, nc-transcript-variant	Fbxw10	Mm_Celera	11:62874777	ACCCTGAACCAGCGC[A/G]TTCCTGGGGCCACTG	213980
rs26941025	snp	C/T	0.5	0	intron-variant	Fbxw10	Mm_Celera	11:62874343	CAAAGAGTCAGGCAA[C/T]AGAAGTCACCATGCT	213980
rs26941026	snp	C/T	0.498615	0.0262793	intron-variant, downstream-variant-500B	Fbxw10	GRCm38.p3	11:62873819	CTCCTTAATGGGACC[C/T]GATCCCCCAAACTCT	213980
rs26941027	snp	G/T	0.32	0.24	intron-variant, downstream-variant-500B	Fbxw10	Mm_Celera	11:62873729	CAGTCAGAGCTGTGT[G/T]TACGCTTAAGTGGGG	213980
rs26941028	snp	A/C	0.35503	0.226867	intron-variant, downstream-variant-500B	Fbxw10	GRCm38.p3	11:62873608	CCTCTGGGACTCTGG[A/C]TTCATTGGCAGAGCA	213980
rs26941029	snp	C/T	0.391111	0.206368	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	Fbxw10	Mm_Celera	11:62873413	CCTCCGGGTCATCAG[C/T]GCCTGTGGAGACGGC	213980
rs26941030	snp	C/T	0.444444	0.157135	intron-variant, stop-lost	Fbxw10	GRCm38.p3	11:62873368	TGTTGTCTTCCCTTC[C/T]AGGGAGGTGCTGCAG	213980
rs26941031	snp	C/T	0.244898	0.249948	intron-variant	Fbxw10	Mm_Celera	11:62873283	AGGCTGGAAACTCTA[C/T]CTCAAGGTCAGGGGT	213980
rs26941032	snp	C/G	0.489796	0.070696	intron-variant	Fbxw10	GRCm38.p3	11:62873191	TCCCCTGCGACCTGC[C/G]ATTAAACCGTGAATA	213980
rs26941033	snp	G/T	0.489796	0.070696	intron-variant	Fbxw10	Mm_Celera	11:62872625	GCATCTATCTGAGGT[G/T]TTCCCTGGCTCCCTC	213980
rs26941034	snp	A/T	0.487535	0.077957	intron-variant	Fbxw10	Mm_Celera	11:62872588	AACTTGATCCCTGTA[A/T]TTGGAGAAAGATTCT	213980
rs26941035	snp	C/T	0.391111	0.206368	intron-variant	Fbxw10	Mm_Celera	11:62870221	TACTGCCACTCTCCA[C/T]GGATGTCTCACCACC	213980
rs26941036	snp	G/T	0.336735	0.234472	intron-variant	Fbxw10	Mm_Celera	11:62869914	TGAATGCTCTTTGTG[G/T]CACATGATAACTACA	213980
rs26941037	snp	A/G	0.359862	0.224567	intron-variant	Fbxw10	GRCm38.p3	11:62868936	GGTTCCACTAAAGAC[A/G]CCTCCAAGTCTGGCC	213980
rs26941038	snp	A/C	0.359862	0.224567	intron-variant	Fbxw10	GRCm38.p3	11:62868776	GAACAAGAACTTAAC[A/C]TTAGTCATATTCCTC	213980
rs26941039	snp	A/G	0.244898	0.249948	intron-variant	Fbxw10	Mm_Celera	11:62868572	TAGGTAGGACCACAT[A/G]ACCACAGTGAAATGT	213980
rs26941040	snp	A/G	0.32	0.24	intron-variant	Fbxw10	GRCm38.p3	11:62868468	GCATGGATTCTGTGT[A/G]GTGCATCCAAACCAC	213980
rs26941041	snp	C/T	0.35503	0.226867	intron-variant	Fbxw10	Mm_Celera	11:62868420	TGTGAAGTTTGAACA[C/T]TGGCTTATGGATTAG	213980
rs26941042	snp	C/T	0.48	0.0979796	intron-variant	Fbxw10	Mm_Celera	11:62868043	CTGCCATGGCCCTAG[C/T]TGGTGGTCCGGAAAA	213980
rs26941043	snp	C/G	0.429688	0.173817	intron-variant	Fbxw10	Mm_Celera	11:62867992	GCAGAGGTAGAGTAC[C/G]CTTCCAGTACGAGCA	213980
rs26941044	snp	C/T	0.444444	0.157135	intron-variant	Fbxw10	GRCm38.p3	11:62867404	TGGTTTTCTCAAGGG[C/T]CAGTTGTCAGGTGAA	213980
rs26941045	snp	A/C	0.459184	0.136902	intron-variant	Fbxw10	GRCm38.p3	11:62867305	TCAGCAGCAAAGACA[A/C]TCCAGGCTTATTGGG	213980
rs26941046	snp	A/G	0.489796	0.070696	intron-variant	Fbxw10	Mm_Celera	11:62867198	CCTAGAGAGGATGAC[A/G]GCTCTGTTTGTGGAC	213980
rs26941047	snp	A/C	0.444444	0.157135	intron-variant	Fbxw10	GRCm38.p3	11:62867101	TTGCTCTAACCCAGT[A/C]TGCAGAGAAGCAGTA	213980
rs26941048	snp	C/G	0.336735	0.234472	intron-variant	Fbxw10	Mm_Celera	11:62866711	ACAAGGGAATGAAAG[C/G]ACGCTTGCAGAGTGG	213980
rs26941049	snp	A/T	0.48	0.0979796	intron-variant	Fbxw10	Mm_Celera	11:62866678	GTTATAAATGGGGCA[A/T]GATGTCCATATGAAC	213980
rs26941050	snp	G/T	0.375	0.216506	intron-variant	Fbxw10	Mm_Celera	11:62866105	TCTGGTCTTTCAAGA[G/T]CTCTGCCACCTTCCT	213980
rs26941051	snp	C/T	0.5	0	intron-variant	Fbxw10	GRCm38.p3	11:62866054	ACAATTAGCAAAATA[C/T]CATTTCCATCACTCT	213980
rs26941052	snp	C/T	0.336735	0.234472	intron-variant	Fbxw10	Mm_Celera	11:62865771	AGCCTGGAAGCCATC[C/T]AAGAGTCTTGGTCTC	213980
rs26941053	snp	C/T	0.345679	0.230967	intron-variant	Fbxw10	GRCm38.p3	11:62865759	AAGAGCAGCCACAGC[C/T]TGGAAGCCATCTAAG	213980
rs26941054	snp	G/T	0.484429	0.0868505	intron-variant	Fbxw10	GRCm38.p3	11:62865610	GAAAGGGACCCAGAG[G/T]TGCTCAGACTCAGTG	213980
rs26941055	snp	A/C	0.165289	0.235211	intron-variant	Fbxw10	Mm_Celera	11:62865608	AGGAAAGGGACCCAG[A/C]GGTGCTCAGACTCAG	213980
rs26941056	snp	A/G	0.345679	0.230967	intron-variant	Fbxw10	Mm_Celera	11:62865086	TTGGCCGAGGATCCT[A/G]GAGAGATGGATTTGA	213980
rs26941057	snp	C/G	0.35503	0.226867	intron-variant	Fbxw10	Mm_Celera	11:62864466	TCAATGGCATATAGA[C/G]ACATGATAGGTATTT	213980
rs26941058	snp	A/G	0.5	0	intron-variant	Fbxw10	Mm_Celera	11:62863815	GGTCCAGGCTGAAGA[A/G]AGACTTCCAGAGGGG	213980
rs26941059	snp	G/T	0.260355	0.249785	intron-variant	Fbxw10	Mm_Celera	11:62863773	GCAGCATGAGGGAAC[G/T]CGGATGGATGTGGCT	213980
rs26941060	snp	C/T	0.32	0.24	intron-variant	Fbxw10	Mm_Celera	11:62863724	AGGACACCTTAGAAA[C/T]CTGCTGTGGTACCTT	213980
rs26941061	snp	A/T	0.492188	0.0620098	intron-variant	Fbxw10	GRCm38.p3	11:62863712	AGAGGACAAATTAGG[A/T]CACCTTAGAAACCTG	213980
rs26941062	snp	A/G	0.345679	0.230967	intron-variant	Fbxw10	GRCm38.p3	11:62863667	GATGTGAGTTTGGAG[A/G]AACATAGAAGAGGGT	213980
rs26941063	snp	A/G	0.375	0.216506	intron-variant	Fbxw10	GRCm38.p3	11:62863634	CATGCTCTAATGTGT[A/G]CTTGAGACAGTAAGT	213980
rs26941064	snp	A/G	0.391111	0.206368	intron-variant	Fbxw10	Mm_Celera	11:62863606	CATAGGTGTGTTTTC[A/G]GTTTGGACCTGACAT	213980
rs26941065	snp	C/G	0.124444	0.216185	intron-variant	Fbxw10	Mm_Celera	11:62863548	TTCAGGGACTGGTTC[C/G]AGGGCACTTCCTGCA	213980
rs26941066	snp	C/T	0.493827	0.0552116	intron-variant	Fbxw10	GRCm38.p3	11:62863488	AGTTATTTGATGTGG[C/T]TGGACTGTTGTGTGT	213980
rs26941067	snp	A/T	0.391111	0.206368	intron-variant	Fbxw10	Mm_Celera	11:62863434	GACAGTTGTGCATGG[A/T]TGGACAGGAGGATGA	213980
rs26955168	snp	A/G	0.391111	0.206368	intron-variant	Fbxw10	Mm_Celera	11:62863401	TAGAAGATACTCCAC[A/G]CAGAATGGACAAGGA	213980
rs26955169	snp	A/G	0.18	0.24	intron-variant	Fbxw10	Mm_Celera	11:62863234	ACAGTCAGAGCTACA[A/G]TGAGAAAAAAATAGG	213980
rs26955170	snp	A/G	0.487535	0.077957	synonymous-codon, nc-transcript-variant	Fbxw10	Mm_Celera	11:62862735	TGTATCTGGAGCAAA[A/G]GATGGACAGGTGAAA	213980
rs26955171	snp	C/T	0.498615	0.0262793	intron-variant	Fbxw10	GRCm38.p3	11:62862463	TGTTACCGGTTCTAA[C/T]GTGCACACTGTGCTA	213980
rs26955172	snp	A/G	0.231111	0.249285	intron-variant	Fbxw10	Mm_Celera	11:62862366	TCAGAACGGCATCAT[A/G]TCCTTATGCTTTCCA	213980
rs26955173	snp	C/T	0.497778	0.0332592	intron-variant	Fbxw10	GRCm38.p3	11:62861883	CCACTCCTCGGGGTA[C/T]TACCTAACCTCTACC	213980
rs26955174	snp	A/C	0.124444	0.216185	intron-variant	Fbxw10	Mm_Celera	11:62861807	CACTATCAGTCTGCG[A/C]GAGGCTTCATTTCTA	213980
rs26955175	snp	A/G	0.132653	0.220748	intron-variant	Fbxw10	Mm_Celera	11:62861806	TCACTATCAGTCTGC[A/G]CGAGGCTTCATTTCT	213980
rs26955176	snp	A/G	0.231111	0.249285	intron-variant	Fbxw10	Mm_Celera	11:62861790	AGTTCACACTATGCG[A/G]TCACTATCAGTCTGC	213980
rs26955177	snp	A/G	0.132653	0.220748	intron-variant	Fbxw10	Mm_Celera	11:62861789	CAGTTCACACTATGC[A/G]GTCACTATCAGTCTG	213980
rs26955178	snp	A/T	0.124444	0.216185	intron-variant	Fbxw10	Mm_Celera	11:62861653	CAATTACTTTGGTTT[A/T]AAAATGCGGTGGGGT	213980
rs26955179	snp	A/G	0.124444	0.216185	intron-variant	Fbxw10	Mm_Celera	11:62861621	TTCCGTGTGGCTGTC[A/G]TTGCTCAACAGTGTT	213980
rs26955180	snp	C/T	0.497778	0.0332592	intron-variant	Fbxw10	GRCm38.p3	11:62861604	TCTGTTGTATTTCAC[C/T]CTTCCGTGTGGCTGT	213980
rs26955181	snp	A/G	0.244898	0.249948	intron-variant	Fbxw10	Mm_Celera	11:62861528	AAAAAAAAGTCTCCC[A/G]CTAGTCTGCAAGGCT	213980
rs26955182	snp	A/G	0.489796	0.070696	intron-variant	Fbxw10	GRCm38.p3	11:62861422	CTTTCACTTTTAGGT[A/G]TTCAGTCTACCTACA	213980
rs26955183	snp	C/T	0.487535	0.077957	intron-variant	Fbxw10	Mm_Celera	11:62861241	TGGTGTCCGAGTACA[C/T]AAGCTTTGGGCTGTG	213980
rs26955184	snp	G/T	0.124444	0.216185	intron-variant	Fbxw10	Mm_Celera	11:62861221	ATGACCTTGGCTATG[G/T]CACCTGGTGTCCGAG	213980
rs26955185	snp	A/C	0.124444	0.216185	intron-variant	Fbxw10	Mm_Celera	11:62861050	ACTGTACTTTGAAAA[A/C]GCTTGGTCTTGACCT	213980
rs26955186	snp	C/G	0.277778	0.248452	intron-variant	Fbxw10	GRCm38.p3	11:62860085	ATGTCTGGGGCCAGC[C/G]AAAACTAGGTAGCTT	213980
rs26955187	snp	G/T	0.124444	0.216185	intron-variant	Fbxw10	Mm_Celera	11:62860049	GCATAAGGTGAGAGC[G/T]ATAAGGCCATGATCG	213980
rs26955188	snp	C/T	0.391111	0.206368	synonymous-codon, intron-variant, nc-transcript-variant	Fbxw10	Mm_Celera	11:62859963	CGAGTTCCGAGGCCA[C/T]GCCGGCAGCGTCAGG	213980
rs26955189	snp	A/C	0.124444	0.216185	synonymous-codon, intron-variant, nc-transcript-variant	Fbxw10	Mm_Celera	11:62859948	CAAGGAGCTGCCCAT[A/C]GAGTTCCGAGGCCAT	213980
rs26955190	snp	G/T	0.231111	0.249285	intron-variant	Fbxw10	Mm_Celera	11:62859685	GCAGAGTGAAGTAGG[G/T]ATCATCAGGCCCTAT	213980
rs26955191	snp	C/T	0.124444	0.216185	intron-variant	Fbxw10	Mm_Celera	11:62859373	AAGCAAAGGGTAACT[C/T]GCAATCTTCTATATT	213980
rs26955192	snp	A/G	0.124444	0.216185	intron-variant	Fbxw10	Mm_Celera	11:62859218	AATAGCAGTGTTCTC[A/G]ATCACTATTAAAGAT	213980
rs26955193	snp	C/T	0.32	0.24	intron-variant	Fbxw10	Mm_Celera	11:62859052	GTGGGGACAGCACTG[C/T]TCTTTACATGTATGT	213980
rs26955194	snp	C/G	0.391111	0.206368	intron-variant	Fbxw10	Mm_Celera	11:62858150	GCCACTGAGAGACAA[C/G]CACCACTAATATTTG	213980
rs26955195	snp	A/G	0.290657	0.246672	intron-variant	Fbxw10	GRCm38.p3	11:62858106	CCTGTAATCCCAGTT[A/G]GTGTATTGAAAAAGT	213980
rs26955196	snp	G/T	0.124444	0.216185	intron-variant	Fbxw10	Mm_Celera	11:62857833	GATCTTTTAGGACCT[G/T]TGCAGGCCCCTGAGG	213980
rs26955197	snp	C/T	0.231111	0.249285	intron-variant	Fbxw10	Mm_Celera	11:62857555	TTAAACGTCAGCTTA[C/T]GGGCCTCTCTCCAAC	213980
rs26955198	snp	G/T	0.48	0.0979796	intron-variant	Fbxw10	GRCm38.p3	11:62857510	CAAGCTCAAACATGC[G/T]CTAGAACCTTCATCT	213980
rs26955199	snp	C/G	0.231111	0.249285	intron-variant	Fbxw10	Mm_Celera	11:62857407	TATGTGAGCTTGCCC[C/G]TGTGAACTCGTTTTC	213980
rs26955200	snp	C/T	0.231111	0.249285	intron-variant	Fbxw10	Mm_Celera	11:62857380	GTATGCCCATGGCCA[C/T]GTGAGCTTGCCTATG	213980
rs26955201	snp	C/T	0.231111	0.249285	intron-variant	Fbxw10	Mm_Celera	11:62857359	CAAAGGCAGCTGTGA[C/T]TTGGTGTATGCCCAT	213980
rs26955202	snp	C/G	0.231111	0.249285	intron-variant	Fbxw10	Mm_Celera	11:62857325	AAATACAAACTCCTG[C/G]CTTTGTGCGATGGTT	213980
rs26955203	snp	A/G	0.231111	0.249285	intron-variant	Fbxw10	GRCm38.p3	11:62857260	AAGCAGTATCTGAGC[A/G]CTGGACTCAAAGGCA	213980
rs26955204	snp	A/C	0.359862	0.224567	intron-variant	Fbxw10	GRCm38.p3	11:62857249	CGACAAGGGTCAAGC[A/C]GTATCTGAGCGCTGG	213980
rs26955205	snp	A/G	0.231111	0.249285	intron-variant	Fbxw10	Mm_Celera	11:62857238	AGCTGCGAGCACGAC[A/G]AGGGTCAAGCAGTAT	213980
rs26955206	snp	C/T	0.231111	0.249285	intron-variant	Fbxw10	Mm_Celera	11:62857209	GTGTAGGCAAGTGGT[C/T]GACTTTGTAAGTCAG	213980
rs26955207	snp	A/C	0.231111	0.249285	intron-variant	Fbxw10	Mm_Celera	11:62857128	CACCCCGTTGAGATT[A/C]GATAAAACTCACGTT	213980
rs26955208	snp	G/T	0.231111	0.249285	intron-variant	Fbxw10	Mm_Celera	11:62856992	AAGTGTTTGGTTCAG[G/T]CATCTATACTGGAAA	213980
rs26955209	snp	A/G	0.244898	0.249948	intron-variant	Fbxw10	Mm_Celera	11:62856971	GAGGGCTGGGGAGAG[A/G]AATGGAAGTGTTTGG	213980
rs26955210	snp	A/G	0.231111	0.249285	intron-variant	Fbxw10	Mm_Celera	11:62856882	GGCAGACACGATGAC[A/G]ATGGATGACATAGGC	213980
rs26955211	snp	A/G	0.231111	0.249285	intron-variant	Fbxw10	Mm_Celera	11:62856797	GAGCATCTGAAGAAG[A/G]GTCCAGGACATGGAG	213980
rs26955212	snp	C/T	0.359862	0.224567	intron-variant	Fbxw10	GRCm38.p3	11:62856346	AATTTCTTGTATTAC[C/T]AGCTGTGGTAGCACA	213980
rs26955213	snp	A/G	0.231111	0.249285	intron-variant	Fbxw10	Mm_Celera	11:62856277	AGGACTACAGAATCC[A/G]ACCTCCCAGACCATT	213980
rs26955214	snp	A/G	0.345679	0.230967	intron-variant	Fbxw10	GRCm38.p3	11:62855986	CCATTCCTCTTTGTT[A/G]AAGTTCCATTTATTC	213980
rs26955215	snp	A/G/T	0.426035	0.177515	intron-variant	Fbxw10	GRCm38.p3	11:62855953	ATTTAGTACCTAGGC[A/G/T]TTGTAGTTACCCTTA	213980

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