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
rs13468083	snp	A/G			upstream-variant-2KB, downstream-variant-500B	Spsb4, Gm16010	GRCm38.p3	9:97018597	ACCCGGTGCTCCGGG[A/G]ACGGGCGGCCGAGGT	211949
rs13468084	snp	A/G			utr-variant-5-prime, downstream-variant-500B	Spsb4, Gm16010	GRCm38.p3	9:97018272	TGGGCGGCAGTGGCA[A/G]CAGACCTCTCTCCCG	211949
rs29883172	snp	C/T	0.5	0	intron-variant	Spsb4	Mm_Celera	9:96950966	CTCTAGGCTGGGACC[C/T]TCATTAGCTTTGCCG	211949
rs29886786	snp	A/G	0.498615	0.0262793	intron-variant	Spsb4	Mm_Celera	9:96946204	ACATATGGCCTCGAT[A/G]TTTTGCGCTACAGCT	211949
rs30123858	snp	C/T	0.375	0.216506	intron-variant	Spsb4	Mm_Celera	9:96947973	TCACACTCAGTCCTC[C/T]CAGCCAGAGGCAGCT	211949
rs30140826	snp	A/G	0.32	0.24	intron-variant	Spsb4	Mm_Celera	9:96978674	TCTATAAATCTCGGC[A/G]TCATCTTGTTGGCTA	211949
rs30226420	snp	C/T	0.497778	0.0332592	utr-variant-3-prime	Spsb4	Mm_Celera	9:96944561	ACCACAGATGACAGC[C/T]GATCCTCAGCGCCGC	211949
rs30246175	snp	A/G	0.375	0.216506	intron-variant	Spsb4	Mm_Celera	9:96952558	ATGGGTGGTGGATTC[A/G]GGCATGCACAGTAAA	211949
rs30321015	snp	G/T	0.484429	0.0868505	intron-variant	Spsb4	Mm_Celera	9:96948653	TTAGAAGACCTGGGC[G/T]ATAACTGTTTGGCTT	211949
rs30484569	snp	C/G	0.5	0	intron-variant	Spsb4	Mm_Celera	9:96948067	GGATAGGGTGTCGAT[C/G]GCATGGCATAGCCTG	211949
rs33115604	snp	C/T	0.231111	0.249285	intron-variant	Spsb4	Mm_Celera	9:96946456	TAAGCATTCTTTTGG[C/T]AACAGAGTACGTAGG	211949
rs33115605	snp	C/T	0.231111	0.249285	intron-variant	Spsb4	Mm_Celera	9:96946485	GGATTGTGGTCAAAT[C/T]ATAAGGAGCAAACAC	211949
rs33115606	snp	A/G	0.132653	0.220748	intron-variant	Spsb4	Mm_Celera	9:96946596	GGTGCAGTTCTAATG[A/G]GCCACCACCGGAATC	211949
rs33115607	snp	G/T	0.35503	0.226867	intron-variant	Spsb4	Mm_Celera	9:96946624	ATCCAAGTGGGACTC[G/T]CATGAGGGCCAGATA	211949
rs33115608	snp	A/G	0.46875	0.121031	intron-variant	Spsb4	Mm_Celera	9:96946639	TCATGAGGGCCAGAT[A/G]ATACATCCAAGGCCA	211949
rs33115609	snp	A/G	0.244898	0.249948	intron-variant	Spsb4	Mm_Celera	9:96946751	GGAGGCTACCCAGGG[A/G]ATGCCAGCCGTGTAT	211949
rs33115610	snp	C/G	0.336735	0.234472	intron-variant	Spsb4	Mm_Celera	9:96947225	AAGCTTGCATTTAGA[C/G]TGTCATACTGCCCCT	211949
rs33115611	snp	A/G	0.231111	0.249285	intron-variant	Spsb4	Mm_Celera	9:96947267	ATAATAAAAAGGTGG[A/G]CCCAAGGCCAGAGTG	211949
rs33115612	snp	A/G	0.231111	0.249285	intron-variant	Spsb4	Mm_Celera	9:96947413	GCCCACCTCCCTGAC[A/G]ATACTGTAACAGAGG	211949
rs33115613	snp	C/T	0.231111	0.249285	intron-variant	Spsb4	Mm_Celera	9:96947470	CTCACCAGTTGGGTG[C/T]CCAAATCAACTCTGT	211949
rs33115634	snp	A/G	0.244898	0.249948	intron-variant	Spsb4	Mm_Celera	9:96966657	GAATGTCACAGGTCG[A/G]TGCACAGAAACATTA	211949
rs33115635	snp	C/T	0.408163	0.193609	intron-variant	Spsb4	Mm_Celera	9:96966675	CACAGAAACATTAAA[C/T]ATTAAACAACGGAGA	211949
rs33115636	snp	A/G	0.260355	0.249785	intron-variant	Spsb4	Mm_Celera	9:96967088	ATGGGCTAGGTTCAT[A/G]AGATACTTACTTCCT	211949
rs33115637	snp	C/T	0.336735	0.234472	intron-variant	Spsb4	Mm_Celera	9:96967099	TCATAAGATACTTAC[C/T]TCCTGGGAAATCATG	211949
rs33115638	snp	A/G	0.336735	0.234472	intron-variant	Spsb4	Mm_Celera	9:96967216	GCTTCTTGAGCCTGG[A/G]CTATCTAAGACAATG	211949
rs33115639	snp	C/T	0.132653	0.220748	intron-variant	Spsb4	Mm_Celera	9:96967286	CCGACAGAAGGAGAC[C/T]CTTGGAAGGAGGCTG	211949
rs33115640	snp	A/G	0.124444	0.216185	intron-variant	Spsb4	Mm_Celera	9:96967321	GGGCAATGTGTTTTA[A/G]ACCTCAGCTCAAGTG	211949
rs33115641	snp	C/T	0.32	0.24	intron-variant	Spsb4	Mm_Celera	9:96967369	TTGAGCCAGCTCTGA[C/T]GCCAAGTCTTGTTCT	211949
rs33115642	snp	A/G	0.391111	0.206368	intron-variant	Spsb4	Mm_Celera	9:96967470	TTCTCCTCTAAGGAA[A/G]TGTTCCCCAGTCCTG	211949
rs33115643	snp	A/C/T	0.231111	0.249285	intron-variant	Spsb4	Mm_Celera	9:96968903	CAATAGTAACTAAGG[A/C/T]GACTGGTAAGAAAAT	211949
rs33116464	snp	A/G	0.444444	0.157135	intron-variant	Spsb4	Mm_Celera	9:96968930	AAATAGTCTAATGAG[A/G]AAGAATGGACCTGAG	211949
rs33116465	snp	A/G	0.244898	0.249948	intron-variant	Spsb4	Mm_Celera	9:96969028	GATTTCATAAGGGTC[A/G]TGTATGTGACGTGCT	211949
rs33116466	snp	A/G	0.132653	0.220748	intron-variant	Spsb4	Mm_Celera	9:96969039	GGTCATGTATGTGAC[A/G]TGCTCAGGAGTGAGC	211949
rs33116467	snp	A/C	0.244898	0.249948	intron-variant	Spsb4	Mm_Celera	9:96969101	GAACACTGAGAACCC[A/C]AGTGCATGCCTGAAG	211949
rs33116468	snp	C/T	0.231111	0.249285	intron-variant	Spsb4	Mm_Celera	9:96969108	GAGAACCCCAGTGCA[C/T]GCCTGAAGCCACAGG	211949
rs33116469	snp	A/G	0.444444	0.157135	intron-variant	Spsb4	Mm_Celera	9:96969135	CAGGACAGAAACCAT[A/G]TTAGTCACTTTTCTT	211949
rs33116470	snp	C/T	0.35503	0.226867	intron-variant	Spsb4	Mm_Celera	9:96969146	CCATGTTAGTCACTT[C/T]TCTTGTTTCTGTCGA	211949
rs33116471	snp	A/G	0.244898	0.249948	intron-variant	Spsb4	Mm_Celera	9:96969160	TTTCTTGTTTCTGTC[A/G]AGGAAAAAAGGTTTG	211949
rs33116472	snp	A/G	0.408163	0.193609	intron-variant	Spsb4	Mm_Celera	9:96969188	TTGTTTCTGTCTTGC[A/G]GTCCAACATGGTGGG	211949
rs33116473	snp	A/G	0.444444	0.157135	intron-variant	Spsb4	Mm_Celera	9:96969235	GAGGCAGTTGGTCAC[A/G]TTGTGTTTGTAGTCA	211949
rs33116494	snp	A/G	0.260355	0.249785	intron-variant	Spsb4	Mm_Celera	9:96947529	TCTGGGCACGAAGGG[A/G]CCCCAGGTACACGTG	211949
rs33116495	snp	A/G	0.244898	0.249948	intron-variant	Spsb4	Mm_Celera	9:96947552	TACACGTGAACCCAG[A/G]GCGAGCCTCTCATGC	211949
rs33116496	snp	A/G	0.132653	0.220748	intron-variant	Spsb4	Mm_Celera	9:96947677	TGCTCAGGGCGTGTC[A/G]GGTCATATTCAGGAT	211949
rs33116497	snp	C/T	0.142012	0.225474	intron-variant	Spsb4	Mm_Celera	9:96947748	TAGATTTGTGTTTGG[C/T]TTTGCTGGTCAGCTT	211949
rs33116498	snp	C/T	0.336735	0.234472	intron-variant	Spsb4	Mm_Celera	9:96947803	TTGTGACCTGGACAC[C/T]TTCTTTACCTAATAT	211949
rs33116499	snp	C/T	0.231111	0.249285	intron-variant	Spsb4	Mm_Celera	9:96947959	CTCGGAAGCCCAGTT[C/T]ACACTCAGTCCTCTC	211949
rs33116500	snp	G/T	0.475309	0.108333	intron-variant	Spsb4	Mm_Celera	9:96948120	TGCTGAAGAATGCTT[G/T]AAAGCGGTCAGCGCT	211949
rs33116501	snp	G/T	0.132653	0.220748	intron-variant	Spsb4	Mm_Celera	9:96948133	TTTAAAGCGGTCAGC[G/T]CTAGAAGCATCTTTG	211949
rs33116502	snp	C/T	0.231111	0.249285	intron-variant	Spsb4	Mm_Celera	9:96948255	CCCAGTTTTATGCTA[C/T]AAACATCCCAGTCCT	211949
rs33116503	snp	A/G	0.124444	0.216185	intron-variant	Spsb4	GRCm38.p3	9:96948457	TGGCACAGAGACTGA[A/G]TTCATGGCTTCAGCT	211949
rs33117294	snp	A/G	0.132653	0.220748	intron-variant	Spsb4	GRCm38.p3	9:96970471	TGATCATTTTGCTAC[A/G]TGGTTAGAAGCTTAC	211949
rs33117295	snp	A/G	0.124444	0.216185	intron-variant	Spsb4	Mm_Celera	9:96970517	TACTAGGCATGTGTC[A/G]CCTGCTTGTCTGGCT	211949
rs33117296	snp	A/C	0.444444	0.157135	intron-variant	Spsb4	Mm_Celera	9:96970748	CAGGCCATTGGTGGG[A/C]GTCTAGTCTAGTCTA	211949
rs33117297	snp	C/T	0.244898	0.249948	intron-variant	Spsb4	Mm_Celera	9:96970764	GTCTAGTCTAGTCTA[C/T]AGTTCGGTTCCTTCT	211949
rs33117298	snp	C/T	0.231111	0.249285	intron-variant	Spsb4	Mm_Celera	9:96971018	AAGCCACTTACAGAC[C/T]GCAAAAGGCTAAGTA	211949
rs33117299	snp	A/G	0.132653	0.220748	intron-variant	Spsb4	Mm_Celera	9:96971019	AGCCACTTACAGACC[A/G]CAAAAGGCTAAGTAA	211949
rs33117300	snp	A/G	0.408163	0.193609	intron-variant	Spsb4	Mm_Celera	9:96971154	CAAGCCTTAAGTGTC[A/G]CTTTCCCAGGACCTT	211949
rs33117301	snp	A/G	0.124444	0.216185	intron-variant	Spsb4	Mm_Celera	9:96971213	GTGGGTCCAAAGATA[A/G]AAAGTTGCAAAGTTA	211949
rs33117302	snp	C/T	0.391111	0.206368	intron-variant	Spsb4	Mm_Celera	9:96971272	TGTTGGGCACTTCCA[C/T]ACAACTCATGACTGG	211949
rs33117303	snp	A/G	0.231111	0.249285	intron-variant	Spsb4	Mm_Celera	9:96971313	CTCACACCCACTGTG[A/G]CTAGATTTATATATT	211949
rs33117504	snp	A/G	0.124444	0.216185	intron-variant	Spsb4	Mm_Celera	9:96948473	TTCATGGCTTCAGCT[A/G]CTCCTTCGGGCTTCT	211949
rs33117505	snp	C/T	0.132653	0.220748	intron-variant	Spsb4	Mm_Celera	9:96948689	AAAGGAAATGAGATA[C/T]GCAGCATACACAGGT	211949
rs33117506	snp	A/T	0.408163	0.193609	intron-variant	Spsb4	Mm_Celera	9:96949281	AAAGCCTGAGTCTGC[A/T]AACTGTCTCAAGGGA	211949
rs33117507	snp	A/C	0.277778	0.248452	intron-variant	Spsb4	Mm_Celera	9:96949606	GAAGCCTTAGGGAAC[A/C]GTACCAACTTAGGTT	211949
rs33117508	snp	A/G	0.48	0.0979796	intron-variant	Spsb4	Mm_Celera	9:96949607	AAGCCTTAGGGAACC[A/G]TACCAACTTAGGTTT	211949
rs33117509	snp	G/T	0.244898	0.249948	intron-variant	Spsb4	Mm_Celera	9:96949813	TTCAGAGGCAAGACT[G/T]CTCAGAGGAAACACT	211949
rs33117510	snp	A/C	0.5	0	intron-variant	Spsb4	Mm_Celera	9:96952346	AGGGTGGTCCTGATG[A/C]AGGAAGAGGTAAGTA	211949
rs33117511	snp	A/G	0.408163	0.193609	intron-variant	Spsb4	Mm_Celera	9:96953508	GCAGCTCTGGGACTG[A/G]AGCCTCTGCCAGCCT	211949
rs33117512	snp	C/T	0.48	0.0979796	intron-variant	Spsb4	Mm_Celera	9:96953541	TGTGGTTTTAGGAGC[C/T]GTGCTCTAGTTCTTC	211949
rs33117513	snp	A/G	0.444444	0.157135	intron-variant	Spsb4	Mm_Celera	9:96953562	CTAGTTCTTCCATCA[A/G]AGGACACCTGGAGGG	211949
rs33118094	snp	A/G	0.444444	0.157135	intron-variant	Spsb4	Mm_Celera	9:96971380	ATGTGACGAAGTGTC[A/G]GTCTCTGTCTGGCCT	211949
rs33118095	snp	A/C	0.124444	0.216185	intron-variant	Spsb4	Mm_Celera	9:96971779	TCCCTCCCTCAGGGT[A/C]GAAGAGTGGCTCTCT	211949
rs33118096	snp	C/T	0.408163	0.193609	intron-variant	Spsb4	Mm_Celera	9:96971869	GGTCCTAGATGCTCT[C/T]AGGCAACTAGGGGAA	211949
rs33118097	snp	C/T	0.444444	0.157135	intron-variant	Spsb4	Mm_Celera	9:96971898	AAGCCCCCCCTGGCA[C/T]TGGTTAACAACCACC	211949
rs33118098	snp	A/G	0.231111	0.249285	intron-variant	Spsb4	Mm_Celera	9:96972280	TCTGATGGCATCCTC[A/G]TGACTAGTGTCAGGC	211949
rs33118099	snp	A/G	0.444444	0.157135	intron-variant	Spsb4	Mm_Celera	9:96972303	TGTCAGGCATGTGCC[A/G]TGCAGTGGCCCTGGG	211949
rs33118100	snp	C/T	0.32	0.24	intron-variant	Spsb4	Mm_Celera	9:96972332	GGAGGGTCTCTGCTT[C/T]ATCCTTCAACAGGCC	211949
rs33118101	snp	A/G	0.231111	0.249285	intron-variant	Spsb4	Mm_Celera	9:96972464	TCAAATAGAAACCAT[A/G]TAGAGTTCAACCTAC	211949
rs33118102	snp	C/T	0.124444	0.216185	intron-variant	Spsb4	Mm_Celera	9:96972534	TCCATACCATCCCTT[C/T]CCTGTGACTAAACAC	211949
rs33118103	snp	A/G	0.124444	0.216185	intron-variant	Spsb4	Mm_Celera	9:96972615	CTATAGGACGACGGC[A/G]CCTCATATGAAGGCA	211949
rs33118444	snp	A/G	0.5	0	intron-variant	Spsb4	Mm_Celera	9:96954089	TCTGACCCAGAGGAA[A/G]AGAATTTTTGCCCAC	211949
rs33118445	snp	A/G	0.48	0.0979796	intron-variant	Spsb4	Mm_Celera	9:96954090	CTGACCCAGAGGAAA[A/G]GAATTTTTGCCCACT	211949
rs33118446	snp	A/G	0.48	0.0979796	intron-variant	Spsb4	Mm_Celera	9:96954092	GACCCAGAGGAAAAG[A/G]ATTTTTGCCCACTAT	211949
rs33118447	snp	A/G	0.197531	0.244432	intron-variant	Spsb4	Mm_Celera	9:96954252	AGGCTAGCTGGCACC[A/G]TTTCCAAATAGCCAA	211949
rs33118448	snp	A/C	0.277778	0.248452	intron-variant	Spsb4	Mm_Celera	9:96954882	ACAACACCCAGCAAA[A/C]CAAAAAGCACATACC	211949
rs33118449	snp	C/T	0.48	0.0979796	intron-variant	Spsb4	Mm_Celera	9:96955389	AAACTTGGCTTCTTG[C/T]TGGGTCCTACTGCCA	211949
rs33118450	snp	C/G/T	0.32	0.24	intron-variant	Spsb4	Mm_Celera	9:96955508	AGGATGGTCAGGAGA[C/G/T]TGGGCAGAGGACACA	211949
rs33118451	snp	C/T	0.48	0.0979796	intron-variant	Spsb4	Mm_Celera	9:96955694	CTCATCTACTCTTCA[C/T]ACGCCTCAGCAGCTT	211949
rs33118452	snp	A/G	0.21875	0.248039	intron-variant	Spsb4	Mm_Celera	9:96955728	GTACAGGCAAGGAAG[A/G]CTCTGTCCTGCCTCC	211949
rs33118453	snp	G/T	0.197531	0.244432	intron-variant	Spsb4	Mm_Celera	9:96956336	TTTGTACCGGCAAAC[G/T]GAGACATTTCCACGC	211949
rs33118544	snp	C/T	0.124444	0.216185	intron-variant	Spsb4	Mm_Celera	9:96992069	AATTTTAGTGATTAA[C/T]TTTATAAAGGGCTTA	211949
rs33118545	snp	A/G	0.231111	0.249285	intron-variant	Spsb4	Mm_Celera	9:96992387	TTCTACACCATGTAC[A/G]ATTCTATTCATCAGG	211949
rs33118546	snp	C/T	0.231111	0.249285	intron-variant	Spsb4	Mm_Celera	9:96992441	CAAGAGGAAATTGCA[C/T]GGTCAGGACGCTCTT	211949
rs33118547	snp	C/T	0.124444	0.216185	intron-variant	Spsb4	Mm_Celera	9:96992716	GCTGGTGTGCCTGAT[C/T]ACCCCAAGCACAAGA	211949
rs33118548	snp	A/G	0.124444	0.216185	intron-variant	Spsb4	Mm_Celera	9:96992733	CCCCAAGCACAAGAG[A/G]GGACACTGAGGCTTT	211949
rs33118549	snp	A/G	0.124444	0.216185	intron-variant	Spsb4	Mm_Celera	9:96992744	AGAGGGGACACTGAG[A/G]CTTTGAGAAAGGAGG	211949
rs33118550	snp	C/T	0.391111	0.206368	intron-variant	Spsb4	Mm_Celera	9:96992778	TTCAGGGAGGTGACC[C/T]TAAGAGGCAGGTTTC	211949
rs33118551	snp	C/T	0.391111	0.206368	intron-variant	Spsb4	Mm_Celera	9:96993055	ACCGCTTTGTCCTAC[C/T]TTTATGTCCTGTATG	211949
rs33118552	snp	C/T	0.391111	0.206368	intron-variant	Spsb4	Mm_Celera	9:96993085	GGCTGTGTCCTACCA[C/T]AGTCAGAGCTGGTTC	211949
rs33118553	snp	A/T	0.231111	0.249285	intron-variant	Spsb4	Mm_Celera	9:96993441	GTGTTCTTTCTTTAG[A/T]CTTTCACATCTGCAT	211949

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