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
rs6176182	snp	A/T	0.244898	0.249948	intron-variant	Rnf128	Mm_Celera	X:139637116	AAAAGCTACTTACAT[A/T]AATATGGTTAAATTT	66889
rs6228382	snp	C/T	0.5	0	intron-variant	Rnf128	Mm_Celera	X:139639761	TCCAGACAGATGTTT[C/T]CCTTATAGGAAAAAA	66889
rs6228426	snp	C/T	0.5	0	intron-variant	Rnf128	Mm_Celera	X:139639785	GAAAAAAAGACAGAA[C/T]GTTAGGTTTTAGTTT	66889
rs6228978	snp	A/G	0.5	0	intron-variant	Rnf128	Mm_Celera	X:139639866	AATTCTTTTACCCAT[A/G]AGGGAAATTTTGGTC	66889
rs6229060	snp	A/G	0.5	0	intron-variant	Rnf128	Mm_Celera	X:139639918	GTCATGTTTGTTTTA[A/G]ATAAAGATAGAGGAA	66889
rs6229538	snp	C/T	0.5	0	intron-variant	Rnf128	Mm_Celera	X:139639971	TCTTCACTTCCTGTA[C/T]CTTCTGCATTTTTGT	66889
rs6229593	snp	C/T	0.5	0	intron-variant	Rnf128	Mm_Celera	X:139640002	TCCACGGAAATAGGA[C/T]AGTGAGCCATTAACT	66889
rs6230046	snp	C/T	0.5	0	intron-variant	Rnf128	Mm_Celera	X:139640028	TAACTTCTATCACAC[C/T]GAGTTGTCTGTCATG	66889
rs6254399	snp	A/G	0.5	0	intron-variant	Rnf128	Mm_Celera	X:139569292	CATTTTTTTACCCCA[A/G]ATTATGTAGTTTTCA	66889
rs6292660	snp	C/T	0.5	0	intron-variant	Rnf128	Mm_Celera	X:139665171	TATATATATACCTTC[C/T]ATTGGTAAAGCCAAT	66889
rs6306761	snp	A/G	0.231111	0.249285	missense	Rnf128	Mm_Celera	X:139665457	CCCATGAAGAGGACA[A/G]TCGCAGTGAGACTGC	66889
rs6360498	snp	C/T	0.304688	0.243945	intron-variant	Rnf128	Mm_Celera	X:139668529	CCACTCTAACTTTCT[C/T]AGTCTGACACCCACT	66889
rs13473063	snp	C/T	0.277778	0.248452	utr-variant-3-prime	Rnf128	Mm_Celera	X:139672130	ATTCAGAACCGTCTA[C/T]GAGTAGTCAGGTTTT	66889
rs29254314	snp	A/G	0.124444	0.216185	intron-variant	Rnf128	Mm_Celera	X:139654656	TATTCAAATAAACAT[A/G]CTAGAGAAATAGCAC	66889
rs29254315	snp	A/C	0.124444	0.216185	intron-variant	Rnf128	Mm_Celera	X:139654172	ACAGCTCTTTTCCCC[A/C]CTTAGGAATAGATTC	66889
rs29254316	snp	C/G	0.132653	0.220748	intron-variant	Rnf128	Mm_Celera	X:139652182	GAGGAGAGGTTGTTA[C/G]TATAATACATCTATT	66889
rs29254317	snp	A/G	0.444444	0.157135	intron-variant	Rnf128	Mm_Celera	X:139651722	TGGCATTAAGCTTCT[A/G]TTAAGAAAATTGGTG	66889
rs29254318	snp	A/G	0.231111	0.249285	intron-variant	Rnf128	Mm_Celera	X:139651425	TGTTAAATGCCCGGT[A/G]GTCAAATCCCAGGCA	66889
rs29254319	snp	A/G	0.231111	0.249285	intron-variant	Rnf128	Mm_Celera	X:139651117	CTGCATTTGCTCACA[A/G]ATAGGCATCCTAGGG	66889
rs29254320	snp	A/G	0.124444	0.216185	intron-variant	Rnf128	Mm_Celera	X:139651090	CACTGAAACTACCAC[A/G]TAGCACACACACTGC	66889
rs29254321	snp	A/T	0.444444	0.157135	intron-variant	Rnf128	Mm_Celera	X:139651021	ACTGTTTTATTCAGG[A/T]ATTGTGCATAGCTTT	66889
rs29254322	snp	A/C	0.444444	0.157135	intron-variant	Rnf128	Mm_Celera	X:139650925	TTTAATCGCTGGCAT[A/C]GCCTTTCTGATAAGG	66889
rs29254323	snp	A/G	0.124444	0.216185	intron-variant	Rnf128	Mm_Celera	X:139650828	TTCCTTAGACTGCTA[A/G]TGGTGGCCATCTTTC	66889
rs29254324	snp	A/G	0.260355	0.249785	intron-variant	Rnf128	Mm_Celera	X:139589793	GAAGGTAAGGTCGTT[A/G]TTTATAATTTAAGAG	66889
rs29254325	snp	C/T	0.18	0.24	intron-variant	Rnf128	Mm_Celera	X:139589156	GTGTATTTTTAATTA[C/T]ATACTTCTTAACAAT	66889
rs29254326	snp	A/G	0.32	0.24	intron-variant	Rnf128	Mm_Celera	X:139589086	GGCAATGCTCTTGTA[A/G]CATAGAGAATGAACA	66889
rs29254327	snp	A/G	0.473373	0.11227	intron-variant	Rnf128	GRCm38.p3	X:139588994	TTTTGTATGTGGTCA[A/G]TCCTCAAGCCATGTT	66889
rs29254328	snp	C/T	0.142012	0.225474	intron-variant	Rnf128	Mm_Celera	X:139588699	TCCAGTGTCTTCTGA[C/T]ACCATATGGCAACTC	66889
rs29254329	snp	C/T	0.473373	0.11227	intron-variant	Rnf128	GRCm38.p3	X:139588614	TTTTTTTTGCCAGTT[C/T]GAACACTTTCATCTT	66889
rs29254330	snp	A/G	0.142012	0.225474	intron-variant	Rnf128	Mm_Celera	X:139586506	TGAGTGCCAGATGAT[A/G]ATTTGGAGTGGAGAA	66889
rs29254331	snp	A/T	0.426035	0.177515	intron-variant	Rnf128	GRCm38.p3	X:139584138	TGAAAACTATCATTG[A/T]CTCTTTATCAAAGTA	66889
rs29254332	snp	C/T	0.426035	0.177515	intron-variant	Rnf128	GRCm38.p3	X:139583890	GGAAGCAGATTGCAG[C/T]GCTGATCTTGTTTCA	66889
rs29254333	snp	A/T	0.473373	0.11227	intron-variant	Rnf128	GRCm38.p3	X:139583237	CCAGTCATGTAAATA[A/T]TATGATTGGCCAGGG	66889
rs29254754	snp	A/C	0.132653	0.220748	intron-variant	Rnf128	Mm_Celera	X:139579468	CCTCAAATACGCAGC[A/C]AGCTTTCCACCAGAT	66889
rs29254755	snp	C/T	0.124444	0.216185	intron-variant	Rnf128	Mm_Celera	X:139579454	TGCTGTCTCTGAGCC[C/T]TCAAATACGCAGCAA	66889
rs29254756	snp	A/T	0.244898	0.249948	intron-variant	Rnf128	Mm_Celera	X:139579424	ATTGGTCTCTTTCAG[A/T]TTTTCATTCCACAGT	66889
rs29254757	snp	A/G	0.132653	0.220748	intron-variant	Rnf128	Mm_Celera	X:139578207	CAGCTGGAGGGCACA[A/G]TGATGAATTCATGAA	66889
rs29254758	snp	A/G	0.142012	0.225474	intron-variant	Rnf128	Mm_Celera	X:139577820	TTGTTGTGACTAGTG[A/G]TAATTACCTATCTTC	66889
rs29254759	snp	A/G	0.152778	0.230321	intron-variant	Rnf128	Mm_Celera	X:139577559	GACAGAGGTTGGTGT[A/G]GTTGGGGACACAGTG	66889
rs29254760	snp	A/G	0.142012	0.225474	intron-variant	Rnf128	Mm_Celera	X:139577508	TGTTGTATGTCACAA[A/G]CATGTGAAAGAAGCA	66889
rs29254761	snp	A/T	0.142012	0.225474	intron-variant	Rnf128	Mm_Celera	X:139575714	GTCAGGGATAAAAAA[A/T]AACCCAACAGGCCAG	66889
rs29254762	snp	C/T	0.408163	0.193609	intron-variant	Rnf128	GRCm38.p3	X:139575687	TCAGTAGCGGAGATA[C/T]AAAAATGACAGGTCA	66889
rs29254763	snp	A/G	0.426035	0.177515	intron-variant	Rnf128	GRCm38.p3	X:139575396	AGATTGTAAGGTGAG[A/G]GTGAGTGTTGGAAGG	66889
rs29254874	snp	A/C	0.444444	0.157135	intron-variant	Rnf128	Mm_Celera	X:139650699	AATTTACAATCACAC[A/C]ACGATTTCTAAAGGT	66889
rs29254875	snp	C/T	0.444444	0.157135	intron-variant	Rnf128	Mm_Celera	X:139650308	GGTTGGGGCTACAGC[C/T]GGGTATAACCATACC	66889
rs29254876	snp	C/T	0.124444	0.216185	intron-variant	Rnf128	Mm_Celera	X:139650213	TTTTGAAAACATTTA[C/T]GTCTCAAACCATAAC	66889
rs29254877	snp	C/G	0.444444	0.157135	intron-variant	Rnf128	Mm_Celera	X:139649848	AGATTGGGTTTTACT[C/G]CTGCTGGTATGTTTT	66889
rs29254878	snp	C/T	0.408163	0.193609	intron-variant	Rnf128	Mm_Celera	X:139649621	GTGTTTACATGTATG[C/T]ACTTGCCTAAATTTG	66889
rs29254879	snp	A/T	0.231111	0.249285	intron-variant	Rnf128	Mm_Celera	X:139649193	CCTAGATAGAGACAT[A/T]CCACACATCTCCCTA	66889
rs29254880	snp	A/G	0.444444	0.157135	intron-variant	Rnf128	Mm_Celera	X:139649108	ACCAGCTGCAAGCAA[A/G]ATGATCCTAGCTACC	66889
rs29254881	snp	C/T	0.124444	0.216185	intron-variant	Rnf128	Mm_Celera	X:139649089	CTGCCTTTCAGACAG[C/T]ATGACCAGCTGCAAG	66889
rs29254882	snp	C/G	0.444444	0.157135	intron-variant	Rnf128	Mm_Celera	X:139648801	AGGTACCACACGATG[C/G]TTTTGTTGTAAAAAG	66889
rs29254883	snp	C/T	0.444444	0.157135	intron-variant	Rnf128	GRCm38.p3	X:139648700	GCAACATATAAAATA[C/T]GAATATAACAGCATA	66889
rs29255294	snp	C/T	0.142012	0.225474	intron-variant	Rnf128	Mm_Celera	X:139575271	CACTGAAAATTAGTA[C/T]AGGAACATTATGGCC	66889
rs29255295	snp	C/T	0.142012	0.225474	intron-variant	Rnf128	Mm_Celera	X:139575251	AGGATGTGGACCATG[C/T]AAAGCACTGAAAATT	66889
rs29255296	snp	A/G	0.142012	0.225474	intron-variant	Rnf128	Mm_Celera	X:139575040	CTCTGTTACTTGTTC[A/G]CTAAGTATTCAAAGT	66889
rs29255297	snp	C/T	0.142012	0.225474	intron-variant	Rnf128	Mm_Celera	X:139574712	TGATAATACATTTTA[C/T]ACCCAAATAATTAAT	66889
rs29255298	snp	G/T	0.142012	0.225474	intron-variant	Rnf128	Mm_Celera	X:139574405	TATGAATGTTCAACA[G/T]TAAAGTGAGGCCAGT	66889
rs29255299	snp	A/G	0.426035	0.177515	intron-variant	Rnf128	Mm_Celera	X:139574393	CTGCTTTCAACATAT[A/G]AATGTTCAACAGTAA	66889
rs29255300	snp	A/C	0.244898	0.249948	intron-variant	Rnf128	Mm_Celera	X:139574219	TTAATTGTGGTACCT[A/C]AAAAACACCTTCAAG	66889
rs29255301	snp	A/G	0.142012	0.225474	intron-variant	Rnf128	Mm_Celera	X:139574150	ACTTTCTGAGTTTTG[A/G]GTTAATTTGTTTAGT	66889
rs29255302	snp	A/C	0.142012	0.225474	intron-variant	Rnf128	Mm_Celera	X:139574113	TAAGACCTCTGTATG[A/C]GGAAGGAGTATGCGA	66889
rs29255303	snp	G/T	0.375	0.216506	intron-variant	Rnf128	GRCm38.p3	X:139574027	CAACAACCTCATTCT[G/T]AGTCCCCCTTCCCAG	66889
rs29255404	snp	A/T	0.231111	0.249285	intron-variant	Rnf128	Mm_Celera	X:139648536	CTGTATTGTGTGTCT[A/T]TGTGTACATGTTTGT	66889
rs29255405	snp	A/C	0.231111	0.249285	intron-variant	Rnf128	Mm_Celera	X:139648492	TGTTGGCCTCTCCAC[A/C]TATTAGGTGTGTTTA	66889
rs29255406	snp	C/T	0.444444	0.157135	intron-variant	Rnf128	Mm_Celera	X:139648472	TCTTTAAGCCTACTT[C/T]TACTTGTTGGCCTCT	66889
rs29255407	snp	C/G	0.152778	0.230321	intron-variant	Rnf128	Mm_Celera	X:139637687	GACAATAAATGGCTG[C/G]ATGTGGTTGAATCTG	66889
rs29255408	snp	C/T	0.124444	0.216185	intron-variant	Rnf128	Mm_Celera	X:139637301	GCTGATTTAAGTTGT[C/T]AGACAAAATGAAGAG	66889
rs29255409	snp	C/T	0.124444	0.216185	intron-variant	Rnf128	Mm_Celera	X:139636738	ATTATGTTGAATTAT[C/T]ATGTCTGATACTAAA	66889
rs29255410	snp	A/G	0.32	0.24	intron-variant	Rnf128	Mm_Celera	X:139636506	ATTGTATGGTTGCAT[A/G]CACTAGATACATTTT	66889
rs29255411	snp	A/G	0.124444	0.216185	intron-variant	Rnf128	Mm_Celera	X:139635972	CAAGACTAATCCACC[A/G]TCAATAACAAATCAT	66889
rs29255412	snp	A/G	0.391111	0.206368	intron-variant	Rnf128	Mm_Celera	X:139635900	ATATATGACTTAAGC[A/G]CAAATTATAAGAGTC	66889
rs29255413	snp	A/G	0.32	0.24	intron-variant	Rnf128	Mm_Celera	X:139635635	TGAACAACAGTTGTA[A/G]ATGCTGTGGGTACTT	66889
rs29255824	snp	C/T	0.375	0.216506	intron-variant	Rnf128	GRCm38.p3	X:139573040	AATGCTTATGGACCC[C/T]GATTTTCAGGTTGAT	66889
rs29255825	snp	C/T	0.152778	0.230321	intron-variant	Rnf128	Mm_Celera	X:139569514	TTTTTATCATTTTGA[C/T]TGTGTCTGATGAAAT	66889
rs29255826	snp	C/T	0.444444	0.157135	intron-variant	Rnf128	GRCm38.p3	X:139569352	ACTAAGCATGAAAAA[C/T]GCACATTTATTCTCA	66889
rs29255827	snp	G/T	0.396694	0.202437	intron-variant	Rnf128	GRCm38.p3	X:139569251	CAAAATCAATATTTT[G/T]GGAAGGACAAACTAG	66889
rs29255828	snp	A/G	0.444444	0.157135	intron-variant	Rnf128	GRCm38.p3	X:139569110	TTGCTGAACAGCCCA[A/G]GTTTTTTTTTTGTTT	66889
rs29255829	snp	A/G	0.486111	0.0821678	intron-variant	Rnf128	GRCm38.p3	X:139568181	CAATAAAGCCCAAGG[A/G]AGGGTGACTTCTTGT	66889
rs29255830	snp	A/G	0.152778	0.230321	intron-variant	Rnf128	Mm_Celera	X:139568077	TAGAAATAGGGTTAC[A/G]TAGCCATTGAGTAAG	66889
rs29255831	snp	A/G	0.165289	0.235211	intron-variant	Rnf128	GRCm38.p3	X:139568039	CTACTTCTTGTTATC[A/G]ACAGAAGCCATTTTC	66889
rs29255832	snp	C/T	0.486111	0.0821678	intron-variant	Rnf128	GRCm38.p3	X:139567593	GTGTTTGACTTGGCA[C/T]TTTTTATTTTATTTT	66889
rs29255833	snp	C/T	0.375	0.216506	intron-variant	Rnf128	GRCm38.p3	X:139567372	TTACTTCACTCCTTG[C/T]TCATCAGAGTTTTGT	66889
rs29255944	snp	C/T	0.32	0.24	intron-variant	Rnf128	Mm_Celera	X:139635508	ACCTTGTCATTGGAA[C/T]AATAGCAATGCCTAC	66889
rs29255945	snp	C/G	0.32	0.24	intron-variant	Rnf128	Mm_Celera	X:139635037	GGTGGCCTTCTGGAG[C/G]CCTTGCGTTTCATTC	66889
rs29255946	snp	A/T	0.231111	0.249285	intron-variant	Rnf128	Mm_Celera	X:139635016	AAGTGCTTGCCTGTC[A/T]GTCTTGGTGGCCTTC	66889
rs29255947	snp	C/T	0.124444	0.216185	intron-variant	Rnf128	Mm_Celera	X:139634919	CAAAGCTTGGCTAGG[C/T]TTGCTTTAGGAGGAC	66889
rs29255948	snp	C/G	0.124444	0.216185	intron-variant	Rnf128	Mm_Celera	X:139634210	ATAGGCAAATAAAAT[C/G]ATAATCTGGCCTGGT	66889
rs29255949	snp	A/C	0.391111	0.206368	intron-variant	Rnf128	Mm_Celera	X:139634177	TGGATGGAGAGTGGC[A/C]GTGCCTCATTCTCCC	66889
rs29255950	snp	A/C	0.124444	0.216185	intron-variant	Rnf128	Mm_Celera	X:139634072	AGGGACACAGATTCA[A/C]CAAAACAAGTTGCTT	66889
rs29255951	snp	A/C	0.277778	0.248452	intron-variant	Rnf128	Mm_Celera	X:139633911	AAAACTAGATAACTC[A/C]CCAACGTATAAAACT	66889
rs29255952	snp	A/T	0.124444	0.216185	intron-variant	Rnf128	Mm_Celera	X:139633644	CTGCTGGTTCTAAAG[A/T]AGAGAATTATTACAG	66889
rs29255953	snp	A/G	0.231111	0.249285	intron-variant	Rnf128	Mm_Celera	X:139633603	ATTGGCACTGATTTG[A/G]TCACCTGAGCTATCC	66889
rs29256324	snp	A/G	0.152778	0.230321	intron-variant	Rnf128	Mm_Celera	X:139566497	CCTGTGAACCTGACC[A/G]CTCACTCCTCCCTGG	66889
rs29256325	snp	A/G	0.375	0.216506	intron-variant	Rnf128	GRCm38.p3	X:139565324	AAACCTCTTTAAAAG[A/G]CATGTGGACCATCGT	66889
rs29256326	snp	A/G	0.46281	0.131194	intron-variant	Rnf128	GRCm38.p3	X:139565205	TTACATAGTAGTCCT[A/G]TTCTCAAACTTTTCT	66889
rs29256327	snp	C/T	0.48	0.0979796	intron-variant	Rnf128	GRCm38.p3	X:139564663	AGAAAACAACAGAGC[C/T]GGAGTTCATCATGGC	66889
rs29256328	snp	A/T	0.152778	0.230321	intron-variant	Rnf128	Mm_Celera	X:139564515	ATCTATCTACCTCAT[A/T]AATCGTGCAAGGGAA	66889
rs29256329	snp	C/T	0.35503	0.226867	intron-variant	Rnf128	GRCm38.p3	X:139564174	ACTGAGCATTTACCT[C/T]CACCAGCATCAAAAT	66889
rs29256330	snp	A/G	0.489796	0.070696	upstream-variant-2KB	Rnf128	GRCm38.p3	X:139562977	TCAGCTCAACTGGTT[A/G]ATAGCATATTTCGGC	66889

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