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
rs3023747	snp	C/T	0.5	0	intron-variant, utr-variant-5-prime	Rnf125	GRCm38.p3	18:20961338	TCCAGTGGGTGTTCT[C/T]AAACTGCACTTATCG	67664
rs6161813	snp	A/C	0.5	0	utr-variant-3-prime	Rnf125	Mm_Celera	18:20983846	gaggtggctaataag[A/C]ccataaaaaaaaaaa	67664
rs29536137	snp	C/G	0.32	0.24	intron-variant	Rnf125	Mm_Celera	18:20949268	CTCCTGAGTCAGAAC[C/G]TGGGGGAGTTCTCAC	67664
rs29536512	snp	A/G	0.375	0.216506	upstream-variant-2KB	Rnf125	GRCm38.p3	18:20943629	GAATGGGGGAGAATG[A/G]GAAGAAGAACATACA	67664
rs29542112	snp	C/T	0.375	0.216506	intron-variant	Rnf125	GRCm38.p3	18:20965695	CTCTGTGAGTGAACT[C/T]ACATAGATCCACCTG	67664
rs29556137	snp	C/T	0.375	0.216506	intron-variant	Rnf125	GRCm38.p3	18:20950200	ACTTTTTTTTTTTTT[C/T]CCCTTAATGTTGCAA	67664
rs29560553	snp	A/G	0.444444	0.157135	intron-variant	Rnf125	GRCm38.p3	18:20955471	GAAAAGTCTGTCTAT[A/G]TAATTAAAATTGTGT	67664
rs29576498	snp	A/G	0.32	0.24	intron-variant	Rnf125	Mm_Celera	18:20953336	GGAAGTGGGGAGGGC[A/G]TTGTTGGAAGATACC	67664
rs29623486	snp	A/G	0.375	0.216506	intron-variant	Rnf125	Mm_Celera	18:20966494	AACTAACCAGTACCC[A/G]GGAGCTCTTGTCTTT	67664
rs29630645	snp	C/T	0.444444	0.157135	intron-variant	Rnf125	GRCm38.p3	18:20949791	GTCAGCGCCATCTTG[C/T]AACGGCGAATGTGAG	67664
rs29676617	snp	C/T	0.498615	0.0262793	intron-variant	Rnf125	GRCm38.p3	18:20951741	GCATTGAAGAGGGGG[C/T]AGCACATTTCACAAG	67664
rs29677704	snp	C/T	0.375	0.216506	intron-variant	Rnf125	GRCm38.p3	18:20951883	AATAAGAAAGTAGGG[C/T]CGGGCATGGTGGCCC	67664
rs29721298	snp	C/T	0.473373	0.11227	intron-variant	Rnf125	GRCm38.p3	18:20947090	GTATGTTTCAGCAGC[C/T]TAGTGATTCAGTTTT	67664
rs29724880	snp	C/T	0.32	0.24	intron-variant	Rnf125	GRCm38.p3	18:20949118	TAAATACCCCCTTAT[C/T]CAGCTACTCGGGGCA	67664
rs29766991	snp	A/C	0.375	0.216506	intron-variant	Rnf125	GRCm38.p3	18:20952217	TATGGACCATAATTA[A/C]TAAGTGGACCACACC	67664
rs29816659	snp	A/C	0.5	0	intron-variant	Rnf125	Mm_Celera	18:20979925	GCCTGATCTACAGAG[A/C]ACATTCCAGGATATT	67664
rs29816850	snp	C/T	0.32	0.24	intron-variant	Rnf125	GRCm38.p3	18:20964475	ATTTTGACAGAGTCC[C/T]ACATATTCCAGCTGA	67664
rs29826613	snp	C/T	0.484429	0.0868505	intron-variant	Rnf125	GRCm38.p3	18:20965416	GTTTTGGAGGTTTTG[C/T]TCTAGTAGTCGGGCA	67664
rs29861797	snp	A/G	0.375	0.216506	intron-variant	Rnf125	GRCm38.p3	18:20949560	CTGGAATCTTCTGTG[A/G]CAAAAGCTTTATTCC	67664
rs29868271	snp	C/T	0.426035	0.177515	upstream-variant-2KB	Rnf125	GRCm38.p3	18:20942758	AGCAACACCCAGCAG[C/T]GTGAAGTCGCTGGAG	67664
rs29879698	snp	C/T	0.444444	0.157135	intron-variant	Rnf125	Mm_Celera	18:20950668	GGGGGGGGGGGACGA[C/T]GACAAACCAAACCTC	67664
rs29882304	snp	C/T	0.375	0.216506	intron-variant	Rnf125	GRCm38.p3	18:20961888	GTAGAAGCAGGAGTA[C/T]TGGGGAAACTAATGC	67664
rs29882311	snp	C/T	0.32	0.24	intron-variant	Rnf125	Mm_Celera	18:20949278	AGAACGTGGGGGAGT[C/T]CTCACGTTGTGGGTC	67664
rs29918357	snp	C/G	0.5	0	intron-variant	Rnf125	GRCm38.p3	18:20946957	AGCCTGGTCTACAGA[C/G]TGAGTTTCAGGACAG	67664
rs29925965	snp	C/G	0.375	0.216506	intron-variant	Rnf125	GRCm38.p3	18:20964865	CACTTTGTAGACCAG[C/G]CTGGCCTCGAACTCA	67664
rs29963782	snp	C/T	0.375	0.216506	intron-variant	Rnf125	GRCm38.p3	18:20951269	CTTGACTCAGATTTA[C/T]TACGTAGCACGGACC	67664
rs30012563	snp	A/G	0.444444	0.157135	intron-variant	Rnf125	Mm_Celera	18:20952942	CCCACGTCTATTTAT[A/G]TACTCCAGTTTTCCA	67664
rs30018989	snp	G/T	0.444444	0.157135	intron-variant	Rnf125	Mm_Celera	18:20964091	TTTTTTTTTTTTTGG[G/T]TTTTCGAGACAGGGT	67664
rs30021682	snp	A/T	0.444444	0.157135	intron-variant	Rnf125	GRCm38.p3	18:20944850	GCAATCTCTCTACCT[A/T]AATTTCGAAATTCCC	67664
rs30064414	snp	A/G/T	0.426035	0.177515	intron-variant	Rnf125	GRCm38.p3	18:20964677	GCCATCCTTACCGAC[A/G/T]AGCACTCTCTTCTGC	67664
rs30065567	snp	A/G	0.49827	0.0293608	upstream-variant-2KB	Rnf125	GRCm38.p3	18:20942802	GCAGGAATGAGCTCC[A/G]GTCTTGTGACAACTT	67664
rs30070394	snp	C/T	0.375	0.216506	intron-variant	Rnf125	GRCm38.p3	18:20948849	CGACATTCCTCCACC[C/T]ACCCGCTTCCTGGGT	67664
rs30079670	snp	A/T	0.444444	0.157135	intron-variant	Rnf125	GRCm38.p3	18:20949775	ACTTAGAACACAGGA[A/T]GTCAGCGCCATCTTG	67664
rs30112462	snp	A/G	0.444444	0.157135	intron-variant	Rnf125	GRCm38.p3	18:20949871	AGGATGGGCCTCAGC[A/G]TGGAGAGGGGTTCTG	67664
rs30178609	snp	G/T	0.5	0	intron-variant	Rnf125	GRCm38.p3	18:20947147	AGGTTCTGGTGTGTG[G/T]TTTTTTTTGTTTTTT	67664
rs30215343	snp	C/T	0.444444	0.157135	intron-variant	Rnf125	GRCm38.p3	18:20949946	ATGGGTCCAAGCTGA[C/T]GGCCTGTGTTCTGCT	67664
rs30267205	snp	C/T	0.426035	0.177515	intron-variant	Rnf125	GRCm38.p3	18:20965354	CCCAGGATACAGGAG[C/T]GGAGGCAAGAGGATA	67664
rs31302717	snp	A/G	0.408163	0.193609	utr-variant-3-prime	Rnf125	Mm_Celera	18:20983322	TTATGTTGCATTCAA[A/G]AACCGTGTTCATTCT	67664
rs31302719	snp	A/G	0.444444	0.157135	utr-variant-3-prime	Rnf125	Mm_Celera	18:20983279	TTGATGGAGAAACAT[A/G]TACTACAGTATTACC	67664
rs31302721	snp	A/G	0.277778	0.248452	intron-variant	Rnf125	Mm_Celera	18:20982685	GGAGTCAGGGTTGCC[A/G]AGAACTTATCTTCCA	67664
rs31302723	snp	A/G	0.165289	0.235211	intron-variant	Rnf125	Mm_Celera	18:20982196	AATGCTCGTTATTTA[A/G]CTCTGTCCCCGAGAA	67664
rs31303475	snp	C/G	0.277778	0.248452	intron-variant	Rnf125	Mm_Celera	18:20982144	TTAGCATTCTGAATC[C/G]TAGAGGTGGCCTTAT	67664
rs31303477	snp	A/G	0.165289	0.235211	intron-variant	Rnf125	Mm_Celera	18:20981353	TTATAATCCTCATAA[A/G]TAAATTGAGCATGTA	67664
rs31303479	snp	A/T	0.444444	0.157135	missense	Rnf125	Mm_Celera	18:20981202	ATTCACGACCTGATG[A/T]AAGCCCAAGTACCTT	67664
rs31303481	snp	A/T	0.375	0.216506	intron-variant	Rnf125	Mm_Celera	18:20980718	GACAACTTAAGTACA[A/T]GAAGTGGAAATGAAA	67664
rs31303483	snp	A/G	0.152778	0.230321	intron-variant	Rnf125	Mm_Celera	18:20979384	ACAGCGTCTGAATTT[A/G]AGATACATTATAAAC	67664
rs31303785	snp	C/G	0.297521	0.245442	intron-variant	Rnf125	GRCm38.p3	18:20945762	CAAGGACTAGAAAAT[C/G]AAGGACTGTTTCAGC	67664
rs31303787	snp	C/T	0.32	0.24	intron-variant	Rnf125	Mm_Celera	18:20945412	GCACACAGTAAAAAT[C/T]CCATAAAAATAACTG	67664
rs31303789	snp	C/T	0.21875	0.248039	intron-variant	Rnf125	Mm_Celera	18:20945073	GACCAGAAGCAGAGA[C/T]GCTCAAAGCGTTTAG	67664
rs31303791	snp	A/T	0.35503	0.226867	intron-variant	Rnf125	Mm_Celera	18:20945012	ATTGGGTGTGAGAAC[A/T]GTATCAGGAAAAGAA	67664
rs31303793	snp	A/T	0.152778	0.230321	intron-variant	Rnf125	Mm_Celera	18:20944779	CACATAAGGCTTCTG[A/T]GTTTTGCATGTCACA	67664
rs31304225	snp	C/T	0.165289	0.235211	intron-variant	Rnf125	Mm_Celera	18:20978949	AAAAAAGGAACTAAC[C/T]TAGCTATGGTCTATG	67664
rs31304227	snp	C/T	0.375	0.216506	intron-variant	Rnf125	Mm_Celera	18:20978315	CTGCTAAGATACATG[C/T]TGTTGCAGAATTTGC	67664
rs31304229	snp	G/T	0.152778	0.230321	intron-variant	Rnf125	Mm_Celera	18:20977241	CTAGATTTGTCTCTT[G/T]CCCACAAAACCTATT	67664
rs31304231	snp	C/G	0.165289	0.235211	intron-variant	Rnf125	Mm_Celera	18:20977094	TGGCATTTACTACTT[C/G]ACTTAATGTGTGAGA	67664
rs31304233	snp	G/T	0.165289	0.235211	intron-variant	Rnf125	Mm_Celera	18:20977033	CCTATGAAGTATGCC[G/T]TGAGTTGTGAAGTCA	67664
rs31304565	snp	G/T	0.165289	0.235211	upstream-variant-2KB	Rnf125	Mm_Celera	18:20944614	TCTTGGAGCTGGGGA[G/T]GCAAACCGGCAGCCT	67664
rs31304567	snp	C/T	0.152778	0.230321	upstream-variant-2KB	Rnf125	Mm_Celera	18:20944532	GTTTCCAAACTTGGA[C/T]GGCGCTTGCCACGTG	67664
rs31304569	snp	C/G	0.375	0.216506	upstream-variant-2KB	Rnf125	Mm_Celera	18:20944224	AAACCTGATCCCCTA[C/G]CTCACACTGGTGTTA	67664
rs31304571	snp	C/T	0.32	0.24	upstream-variant-2KB	Rnf125	Mm_Celera	18:20943912	CGTTCACATTTAAGA[C/T]CTTGAATTAAAAGAA	67664
rs31304573	snp	G/T	0.336735	0.234472	upstream-variant-2KB	Rnf125	Mm_Celera	18:20943898	CCCATTCAATATCTC[G/T]TTCACATTTAAGACC	67664
rs31305075	snp	A/C	0.152778	0.230321	intron-variant	Rnf125	Mm_Celera	18:20976331	GAGGCTCGTTGTCCA[A/C]CATCTCTGCAACAGT	67664
rs31305077	snp	C/G	0.152778	0.230321	intron-variant	Rnf125	Mm_Celera	18:20976164	AAGGTGCTGAAACAA[C/G]TTGCAGCCTGTCGTA	67664
rs31305078	snp	C/G	0.152778	0.230321	intron-variant	Rnf125	Mm_Celera	18:20976104	TGCTTGTTTGGGGAA[C/G]TCTGCGCCAGTGTTT	67664
rs31305079	snp	C/T	0.152778	0.230321	intron-variant	Rnf125	Mm_Celera	18:20975737	CTGTTTCTGATTTGG[C/T]GCAAGTTATTATTAT	67664
rs31305081	snp	A/G	0.132653	0.220748	missense	Rnf125	Mm_Celera	18:20974433	AGTCAGAATACCAGA[A/G]CTGTGCTGAGTGTGG	67664
rs31305083	snp	A/G	0.260355	0.249785	intron-variant	Rnf125	GRCm38.p3	18:20972303	GTTTTGTTTCCATTC[A/G]GAGTGTTCTTCTCTA	67664
rs31305475	snp	A/C/T	0.21875	0.248039	upstream-variant-2KB	Rnf125	Mm_Celera	18:20943862	TAATTGTTACGTAAA[A/C/T]GATTACAGGAAATTC	67664
rs31305477	snp	C/T	0.165289	0.235211	upstream-variant-2KB	Rnf125	Mm_Celera	18:20943561	CCAGCACTTTGGTGC[C/T]GAAAGAGGAAGATTA	67664
rs31305479	snp	A/T	0.165289	0.235211	upstream-variant-2KB	Rnf125	Mm_Celera	18:20943327	GAGGAGCTTTGTGGA[A/T]GCCTCTGGAGACCTA	67664
rs31305481	snp	C/T	0.244898	0.249948	upstream-variant-2KB	Rnf125	Mm_Celera	18:20943237	CATAGTCCTGGGATG[C/T]AGCAGGACCTTTTTA	67664
rs31305483	snp	C/T	0.260355	0.249785	upstream-variant-2KB	Rnf125	Mm_Celera	18:20943148	CTCAGTTTCACAATC[C/T]GAGGCAATTAGTTAA	67664
rs31306114	snp	C/G	0.18	0.24	intron-variant	Rnf125	Mm_Celera	18:20972185	GCTGATCCTCTGCCT[C/G]CTCGTCTCTCTCAGC	67664
rs31306115	snp	A/G	0.18	0.24	intron-variant	Rnf125	Mm_Celera	18:20971350	TACACTCTGACTCAC[A/G]CAGTGTGGATGGGCT	67664
rs31306116	snp	C/T	0.244898	0.249948	intron-variant	Rnf125	Mm_Celera	18:20971190	TCAACTTTCTGACCA[C/T]GTTCTGAGCAGCTAC	67664
rs31306117	snp	C/G	0.260355	0.249785	intron-variant	Rnf125	Mm_Celera	18:20969148	AGTGCCATTGTTCTA[C/G]TGGGTGAGCACATGT	67664
rs31306119	snp	A/T	0.260355	0.249785	intron-variant	Rnf125	Mm_Celera	18:20968496	TTTTCCTAGAAGGCA[A/T]TGCTGCTGAGGCGAT	67664
rs31306121	snp	A/G	0.244898	0.249948	intron-variant	Rnf125	Mm_Celera	18:20967957	TTTAGAGTCCTAGAA[A/G]ATTGCCACAAGTTTA	67664
rs31306123	snp	C/G	0.277778	0.248452	intron-variant	Rnf125	Mm_Celera	18:20967855	GCCATCACAGGCCTG[C/G]TGAACATTCAGCAAT	67664
rs31306355	snp	A/G	0.231111	0.249285	upstream-variant-2KB	Rnf125	Mm_Celera	18:20942995	TGCCTCTGTTAGGAA[A/G]GTATCTCACAAAGAA	67664
rs31306357	snp	A/C	0.32	0.24	upstream-variant-2KB	Rnf125	Mm_Celera	18:20942867	TAAATAAATGTTGCA[A/C]TCTGAGGACGATACA	67664
rs31306359	snp	C/G	0.124444	0.216185	upstream-variant-2KB	Rnf125	Mm_Celera	18:20942815	CCGGTCTTGTGACAA[C/G]TTCCAAAACAACTAG	67664
rs31306361	snp	C/T	0.132653	0.220748	upstream-variant-2KB	Rnf125	Mm_Celera	18:20942804	AGGAATGAGCTCCGG[C/T]CTTGTGACAACTTCC	67664
rs31307135	snp	A/G	0.142012	0.225474	intron-variant	Rnf125	Mm_Celera	18:20966071	GCATAAATATTAGCT[A/G]CTTTACATGACCAAG	67664
rs31307137	snp	C/T	0.32	0.24	intron-variant	Rnf125	Mm_Celera	18:20966039	GTGTTATAGGCACAG[C/T]CGCTAAAGGGAGCTG	67664
rs31307139	snp	C/T	0.260355	0.249785	intron-variant	Rnf125	Mm_Celera	18:20965917	AAGGAACCTAATTTA[C/T]TGTTGACGAGAACAG	67664
rs31307142	snp	C/T	0.244898	0.249948	intron-variant	Rnf125	Mm_Celera	18:20965389	TTAGGAATTGGCTCT[C/T]CTACCTTGTGTGTTT	67664
rs31307195	snp	A/G	0.244898	0.249948	upstream-variant-2KB	Rnf125	Mm_Celera	18:20942689	TTCAGTTTACTTCAC[A/G]TGCAAGACCCTAAGT	67664
rs31308116	snp	A/G	0.244898	0.249948	intron-variant	Rnf125	Mm_Celera	18:20964027	ATAGTGTGCAAAGAC[A/G]TGACTGCAAGCTGGG	67664
rs31308119	snp	A/C	0.231111	0.249285	intron-variant	Rnf125	Mm_Celera	18:20951617	TGTCCCAGGTTGTCT[A/C]AGTGTTTTGTGACCT	67664
rs31308121	snp	A/G	0.231111	0.249285	intron-variant	Rnf125	Mm_Celera	18:20951360	CCTTTTCAGACATTT[A/G]CTATTACTTTGTGTA	67664
rs31308123	snp	C/T	0.426035	0.177515	intron-variant	Rnf125	Mm_Celera	18:20948071	TCCCAGATTTTTTTT[C/T]TTGGATCACACCCAG	67664
rs31308965	snp	A/T	0.375	0.216506	intron-variant	Rnf125	GRCm38.p3	18:20947986	GAATTACATCTCTAG[A/T]CTCAGACTTTGAATT	67664
rs31308967	snp	C/T	0.142012	0.225474	intron-variant	Rnf125	Mm_Celera	18:20947970	AAGCACTCTCCCGAC[C/T]GAATTACATCTCTAG	67664
rs31308969	snp	A/G	0.18	0.24	intron-variant	Rnf125	Mm_Celera	18:20947714	ACCATACTTGGCCTG[A/G]TGATCTTAACTGTCA	67664
rs31308971	snp	C/T	0.165289	0.235211	intron-variant	Rnf125	Mm_Celera	18:20947239	GGTTGGCTAATTGGA[C/T]TTTGGTTACGGGGAT	67664
rs31308973	snp	A/T	0.18	0.24	intron-variant	Rnf125	Mm_Celera	18:20947100	GCAGCCTAGTGATTC[A/T]GTTTTTGTTGACTGC	67664
rs31309806	snp	A/G	0.426035	0.177515	intron-variant	Rnf125	Mm_Celera	18:20946819	AGCCCAGTGGGAGCA[A/G]CTCAGTAAGGGCCTA	67664
rs31309808	snp	G/T	0.345679	0.230967	intron-variant	Rnf125	GRCm38.p3	18:20946523	GCTCACAGATCTGAC[G/T]ACCGCAGAACCATTA	67664
rs31309810	snp	C/T	0.375	0.216506	intron-variant	Rnf125	Mm_Celera	18:20946461	CTTTGCAGTTAGCTT[C/T]GCCGCAAAAAGCAAG	67664

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