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
rs6254541	snp	A/G	0.21875	0.248039	synonymous-codon, downstream-variant-500B	Trim30d	Mm_Celera	7:104472430	TTGAGCACACTTTCC[A/G]TCATTTAATCCGAGG	209387
rs6255654	snp	C/T	0.32	0.24	missense, utr-variant-3-prime, downstream-variant-500B	Trim30d	Mm_Celera	7:104472620	GCATTGTTCCTTGCA[C/T]GTAGAGTCATATGAA	209387
rs6255756	snp	C/T	0.5	0	intron-variant, downstream-variant-500B	Trim30d	Mm_Celera	7:104472677	TTGAGTCAAATGAAA[C/T]ANAAGGTACAGCCTT	209387
rs6255769	snp	C/T	0.5	0	intron-variant, downstream-variant-500B	Trim30d	Mm_Celera	7:104472679	GAGTCAAATGAAANA[C/T]AAGGTACAGCCTTAT	209387
rs6322810	snp	A/C	0.5	0	intron-variant	Trim30d	Mm_Celera	7:104489025	cagactcacaggatc[A/C]nagagacagctgaac	209387
rs6322811	snp	A/C	0.5	0	intron-variant	Trim30d	Mm_Celera	7:104489026	agactcacaggatcn[A/C]agagacagctgaact	209387
rs31175248	snp	G/T	0.444444	0.157135	intron-variant	Trim30d	Mm_Celera	7:104484735	CTCAGAGATGCAGGA[G/T]CATCAGCTGCCAGGG	209387
rs31192249	snp	G/T	0.32	0.24	intron-variant	Trim30d	GRCm38.p3	7:104507457	GGGAGACCAAAGTCT[G/T]TCTTGGAGCAGAAGG	209387
rs31196368	snp	A/G	0.32	0.24	intron-variant, missense	Trim30d	Mm_Celera	7:104487923	AGTCAGCACTCACAG[A/G]TTCCTTCAAGAGCTC	209387
rs31237531	snp	C/G	0.444444	0.157135	intron-variant	Trim30d	Mm_Celera	7:104488427	CACTGATAGTCAGAA[C/G]AAAGGGTAAGCAGAA	209387
rs31247831	snp	G/T	0.444444	0.157135	intron-variant	Trim30d	Mm_Celera	7:104485195	GTTAGAAAAAAAAGA[G/T]GCATGTGTTGTCTGC	209387
rs31323800	snp	A/C	0.375	0.216506	intron-variant	Trim30d	Mm_Celera	7:104488121	ACCTTGTTCAGATAT[A/C]AAGGAAGGACCATGA	209387
rs31324799	snp	A/G	0.32	0.24	intron-variant	Trim30d	Mm_Celera	7:104507291	TAGTACAAGTACATT[A/G]ATAGGAAGCTACACA	209387
rs31342879	snp	G/T	0.444444	0.157135	utr-variant-3-prime	Trim30d	Mm_Celera	7:104471852	ACAGCTATTTTTTTT[G/T]GGGGGGGGAAATATT	209387
rs31447031	snp	A/G	0.375	0.216506	intron-variant	Trim30d	Mm_Celera	7:104486945	GCTTAGGGCTTAGGG[A/G]TGGATTATATAGCCA	209387
rs31550524	snp	A/G	0.396694	0.202437	intron-variant	Trim30d	Mm_Celera	7:104479645	GAGACATTGATTCTA[A/G]TTGAATATCAACTAA	209387
rs31622485	snp	A/G	0.33241	0.236027	intron-variant	Trim30d	Mm_Celera	7:104487112	TGTTTCTCATTATGG[A/G]AACCTTCCTCTCCTC	209387
rs31639330	snp	A/G	0.32	0.24	intron-variant	Trim30d	Mm_Celera	7:104480595	CTGAATAAGGATAGC[A/G]TAATTTTGTGAATCT	209387
rs31714707	snp	C/T	0.444444	0.157135	intron-variant	Trim30d	Mm_Celera	7:104482382	AAGATGGTAGTATAG[C/T]GGTAGATCTGCCCAA	209387
rs31716116	snp	A/C	0.375	0.216506	intron-variant	Trim30d	Mm_Celera	7:104486411	ACACTACAGCTTTCG[A/C]AATGAGTTTTTCACT	209387
rs31758402	snp	A/C	0.375	0.216506	intron-variant, utr-variant-5-prime	Trim30d	Mm_Celera	7:104488040	TGACTTCTCACACTT[A/C]TGCATGGATGGCTGT	209387
rs31884308	snp	A/G	0.359862	0.224567	intron-variant	Trim30d	Mm_Celera	7:104487473	AACTTCTAAGCCTAT[A/G]ATGCTCAGGTAAGTA	209387
rs31890855	snp	C/T	0.375	0.216506	downstream-variant-500B	Trim30d	Mm_Celera	7:104469552	TTTGATTTGAATTTC[C/T]CTGATGACTGAAGCA	209387
rs31894761	snp	C/T	0.207612	0.24638	utr-variant-3-prime	Trim30d	Mm_Celera	7:104471786	TCATTCTTTTGACTG[C/T]GTTCCTACAGAGATG	209387
rs31924947	snp	A/C	0.375	0.216506	intron-variant	Trim30d	Mm_Celera	7:104486644	AAACAAACCATAAAA[A/C]GAGCTAAGTAAAAAA	209387
rs31936340	snp	C/T	0.124444	0.216185	utr-variant-3-prime	Trim30d	Mm_Celera	7:104470425	AGTACAGCACATTTA[C/T]ACAGTAATTAGCACA	209387
rs31936343	snp	C/T	0.132653	0.220748	utr-variant-3-prime	Trim30d	Mm_Celera	7:104470665	AAAGGGCTTTTACTC[C/T]CAGAGCCTTCTAAAG	209387
rs31936495	snp	G/T	0.124444	0.216185	intron-variant, utr-variant-5-prime	Trim30d	Mm_Celera	7:104488010	TAGTTGCTGTGATCC[G/T]GTGTCTGCCTGTCCT	209387
rs31936497	snp	G/T	0.142012	0.225474	intron-variant	Trim30d	Mm_Celera	7:104488180	TGTGGAAGGAGGTTT[G/T]GTGACATAGCAAATA	209387
rs31936499	snp	C/T	0.495868	0.0452663	intron-variant	Trim30d	Mm_Celera	7:104488209	TAGTACTTTGTCATG[C/T]TTCAGGTGCTGTACT	209387
rs31936501	snp	C/T	0.48	0.0979796	intron-variant	Trim30d	Mm_Celera	7:104488303	AGAAAGAATTTACTG[C/T]CAACATCCTTGCTTG	209387
rs31937206	snp	A/C	0.124444	0.216185	utr-variant-3-prime	Trim30d	Mm_Celera	7:104471179	TACCGTTGTGGACCT[A/C]GGTAGTTCTGTCTGT	209387
rs31937209	snp	C/T	0.124444	0.216185	utr-variant-3-prime	Trim30d	Mm_Celera	7:104471196	GTAGTTCTGTCTGTA[C/T]GACCTGGTGTTTGCA	209387
rs31937212	snp	A/C	0.152778	0.230321	utr-variant-3-prime	Trim30d	Mm_Celera	7:104471312	TATACAAGAGTACTC[A/C]TGAAGGTTTTTTGAG	209387
rs31937534	snp	C/T	0.444444	0.157135	intron-variant	Trim30d	Mm_Celera	7:104499469	CCTGCTGTTGAAAGC[C/T]GTGCATAGGCCTGCA	209387
rs31937537	snp	G/T	0.197531	0.244432	intron-variant	Trim30d	Mm_Celera	7:104507216	CCAAGGACAAGGGCA[G/T]GCTATGGTACTGACT	209387
rs31937540	snp	G/T	0.165289	0.235211	upstream-variant-2KB	Trim30d	Mm_Celera	7:104508339	ATGTGCAGAGACAGG[G/T]AGAAACACCTCACCA	209387
rs31938015	snp	A/G	0.124444	0.216185	utr-variant-3-prime	Trim30d	Mm_Celera	7:104471693	AATGTCCTTGAGGTT[A/G]AAGGCTCTCTGCCCT	209387
rs31938020	snp	C/T	0.124444	0.216185	synonymous-codon, downstream-variant-500B	Trim30d	Mm_Celera	7:104472199	GCAAACTTCCTGGTC[C/T]AGGAAAACTCCTACA	209387
rs31938023	snp	G/T	0.124444	0.216185	missense, downstream-variant-500B	Trim30d	Mm_Celera	7:104472227	ACACGACTGGGACGA[G/T]CAGGCAGAGAGAGGG	209387
rs31939046	snp	A/G	0.124444	0.216185	synonymous-codon, downstream-variant-500B	Trim30d	Mm_Celera	7:104472364	ATTTTGTTTAATATG[A/G]GAATGATATTTTTTT	209387
rs31939053	snp	C/T	0.124444	0.216185	intron-variant, downstream-variant-500B	Trim30d	Mm_Celera	7:104472716	CTTAAGCAACAGAAG[C/T]ATAAGGAGAAAGAGC	209387
rs31939996	snp	C/T	0.124444	0.216185	intron-variant	Trim30d	Mm_Celera	7:104473053	TCATATAGAATGGCA[C/T]CACAGGGACACACTA	209387
rs31939999	snp	A/G	0.277778	0.248452	intron-variant	Trim30d	Mm_Celera	7:104473131	TCTATTTGCCGGCCA[A/G]GCACACCCAGAATCA	209387
rs31940002	snp	C/T	0.124444	0.216185	intron-variant	Trim30d	Mm_Celera	7:104479177	GTCTACCTGCAGCCA[C/T]TGTTTCACTGCCAAA	209387
rs31940807	snp	C/G	0.336735	0.234472	intron-variant	Trim30d	Mm_Celera	7:104479672	CTAATTTTCAACACC[C/G]AATAGGACTATCCTT	209387
rs31940811	snp	A/G	0.260355	0.249785	intron-variant	Trim30d	Mm_Celera	7:104483233	AAGACTACAGGAAGA[A/G]CGCACTGTAATCACC	209387
rs31941814	snp	G/T	0.459184	0.136902	missense	Trim30d	Mm_Celera	7:104483560	ATCACTGTGTATTTG[G/T]TTCTTTAAGGGTGAA	209387
rs31941817	snp	C/T	0.297521	0.245442	intron-variant	Trim30d	Mm_Celera	7:104483777	CCAAAGTAGGATAAC[C/T]GGATATGGCTCAGTT	209387
rs31941820	snp	A/G	0.124444	0.216185	intron-variant	Trim30d	Mm_Celera	7:104484281	AGCTTCTCCTGTGAG[A/G]AAGGAATTGTATCAG	209387
rs31941823	snp	A/G	0.465374	0.126941	intron-variant	Trim30d	Mm_Celera	7:104484339	CTGTTCCTAAGCAAA[A/G]GGCAACAAACTCTTC	209387
rs31942546	snp	C/T	0.124444	0.216185	intron-variant	Trim30d	Mm_Celera	7:104484625	ACATGCCCTACTGTG[C/T]CATATTTGATACCTG	209387
rs31942550	snp	C/G	0.152778	0.230321	intron-variant	Trim30d	Mm_Celera	7:104487157	TGCCACATGCACATT[C/G]TCTTCACTGCTGTGT	209387
rs31942552	snp	A/G	0.124444	0.216185	intron-variant	Trim30d	Mm_Celera	7:104487211	GTTGAAAGTCACTAG[A/G]TGGCATGTTAGGTAC	209387
rs31943726	snp	A/G	0.124444	0.216185	intron-variant, synonymous-codon	Trim30d	Mm_Celera	7:104487633	ACCACTGTGCTCCTG[A/G]GATTGCTTACAAAGC	209387
rs31943729	snp	C/T	0.124444	0.216185	intron-variant, synonymous-codon	Trim30d	Mm_Celera	7:104487732	AACCTTCTGCTCCTC[C/T]TCTGGGATGGACTTG	209387
rs31943732	snp	C/T	0.444444	0.157135	intron-variant, synonymous-codon	Trim30d	Mm_Celera	7:104487963	TGGGCAGGTCACTTC[C/T]TCCTTTATCATCTCC	209387
rs31952492	snp	A/G	0.444444	0.157135	intron-variant	Trim30d	Mm_Celera	7:104484995	CTATTATGGATGGCT[A/G]TGAGACACCATGTGA	209387
rs31975738	snp	A/G	0.375	0.216506	intron-variant	Trim30d	Mm_Celera	7:104487024	ATGCATGCAGCCACA[A/G]TCTCCGTGAGTTTAT	209387
rs31983971	snp	G/T	0.444444	0.157135	utr-variant-3-prime	Trim30d	Mm_Celera	7:104471851	AACAGCTATTTTTTT[G/T]TGGGGGGGGAAATAT	209387
rs32027409	snp	A/G	0.375	0.216506	intron-variant	Trim30d	Mm_Celera	7:104486339	TGACTTGTTGCAATC[A/G]ACATTTGCAAGCAAA	209387
rs32029000	snp	A/G	0.375	0.216506	intron-variant	Trim30d	Mm_Celera	7:104486669	AAAAAAATTCACAAG[A/G]CGTGCATATAGATAT	209387
rs32032377	snp	A/T	0.444444	0.157135	intron-variant	Trim30d	Mm_Celera	7:104482270	GAAAATGGAAGAGGG[A/T]GAGGACGCAGAAGAG	209387
rs32043205	snp	G/T	0.375	0.216506	intron-variant	Trim30d	Mm_Celera	7:104486306	GTAGCAGAAGCCAGA[G/T]GCCTCAGACAATACC	209387
rs32068112	snp	A/G	0.32	0.24	intron-variant	Trim30d	GRCm38.p3	7:104507422	TTCATACACTCCTTT[A/G]GCTGTACTTCTTCTA	209387
rs32102353	snp	A/C	0.375	0.216506	intron-variant	Trim30d	Mm_Celera	7:104484512	GAAATCTCTCTAAGT[A/C]ATTCATCCCACTCAG	209387
rs32227749	snp	A/T	0.32	0.24	intron-variant	Trim30d	Mm_Celera	7:104507219	AGGACAAGGGCAGGC[A/T]ATGGTACTGACTTTT	209387
rs32264645	snp	C/T	0.32	0.24	intron-variant	Trim30d	GRCm38.p3	7:104507405	AATCTTAAAAGTTTG[C/T]TTTCATACACTCCTT	209387
rs32300073	snp	C/T	0.5	0	intron-variant	Trim30d	Mm_Celera	7:104482478	GGAGATTTACCACAA[C/T]ACAGCAAAATTTCCT	209387
rs32336537	snp	A/G	0.444444	0.157135	intron-variant	Trim30d	Mm_Celera	7:104482114	ATTCTCCTGTGAGTG[A/G]CTTTGAACAAGGAAT	209387
rs32425666	snp	A/G	0.375	0.216506	intron-variant	Trim30d	Mm_Celera	7:104486956	AGGGATGGATTATAT[A/G]GCCACTTCTTCCTGT	209387
rs32453198	snp	A/G	0.444444	0.157135	intron-variant	Trim30d	Mm_Celera	7:104475226	GACACAAAATAATCA[A/G]AACAACAAATGCACT	209387
rs45646672	snp	A/G			intron-variant	Trim30d	Mm_Celera	7:104495067	AAAACAGTCCTCAAC[A/G]GATACAAGAATATAT	209387
rs45690160	snp	C/T			intron-variant	Trim30d	Mm_Celera	7:104482383	ATTGGGCAGATCTAC[C/T]GCTACACTGCCATCT	209387
rs45693985	snp	A/T			intron-variant	Trim30d	Mm_Celera	7:104504713	GACTCCATGATCAAC[A/T]ATTTATAAATGGGAC	209387
rs45694148	snp	A/G			intron-variant	Trim30d	GRCm38.p3	7:104507399	CAAAGAAATCTTAAA[A/G]TTTTGCTTTCATACA	209387
rs45699371	snp	C/T			intron-variant	Trim30d	Mm_Celera	7:104494639	AACAAGTTGGTGTAG[C/T]GATTCTAATATCGAA	209387
rs45725512	snp	C/T			intron-variant	Trim30d	Mm_Celera	7:104488967	CCAGGATGTTAGGGT[C/T]CCAGAGGCAGCTTGA	209387
rs45738663	snp	C/T			intron-variant	Trim30d	Mm_Celera	7:104495183	ATGGAAGCTGAACAA[C/T]GCTCTACTCAATGAT	209387
rs45742518	snp	A/T			intron-variant	Trim30d	Mm_Celera	7:104507571	AGAGCTGTCTTCCTT[A/T]AGGCCACCCTGTCTC	209387
rs45861138	snp	A/T			upstream-variant-2KB	Trim30d	GRCm38.p3	7:104508089	TGTATAAATATGGAA[A/T]GAGAGCCTTTCCCAT	209387
rs45874237	snp	C/T			upstream-variant-2KB	Trim30d	Mm_Celera	7:104508421	TGGTCTCCTCCAGAT[C/T]ATGTATTCTGTGGCT	209387
rs45914858	snp	A/G			intron-variant	Trim30d	Mm_Celera	7:104506156	TAGGAACTTGGAGAG[A/G]GGGAGGAGACAAGAC	209387
rs45932673	snp	A/C			intron-variant	Trim30d	Mm_Celera	7:104507653	CCCTCCTGCTTTTTA[A/C]CTCCAACTTAAACTC	209387
rs45936680	snp	C/T			intron-variant	Trim30d	Mm_Celera	7:104506267	TAGCAGAGATGAAAT[C/T]TTCATTTAACAAGTT	209387
rs45979828	snp	A/C/G			intron-variant	Trim30d	GRCm38.p3	7:104507640	TTCCCCTCCAACACC[A/C/G]TCCTGCTTTTTAACT	209387
rs45988125	snp	A/T			intron-variant	Trim30d	Mm_Celera	7:104504705	ATGGCTTAGACTCCA[A/T]GATCAACTATTTATA	209387
rs46022753	snp	G/T			intron-variant	Trim30d	Mm_Celera	7:104488604	GTGGGCCAGTGCCCT[G/T]AGCAGACAACCTTGA	209387
rs46043279	snp	A/C			intron-variant	Trim30d	GRCm38.p3	7:104497263	GTAAAGAGAACTTCT[A/C]AACTTCATATGGAAA	209387
rs46131491	snp	C/T			intron-variant	Trim30d	GRCm38.p3	7:104495965	TATCAATGATTTATT[C/T]GTAATATTTTATGGT	209387
rs46177476	snp	A/C			intron-variant	Trim30d	Mm_Celera	7:104505008	TGCAAATAAAAAAAA[A/C]TAAGGTTTCATCTTA	209387
rs46216191	snp	A/C			intron-variant	Trim30d	Mm_Celera	7:104488607	GGCCAGTGCCCTGAG[A/C]AGACAACCTTGAGCA	209387
rs46240261	snp	A/T			upstream-variant-2KB	Trim30d	Mm_Celera	7:104508689	CTGTACAAAATCAGG[A/T]GTGGTGGCTCCTGCA	209387
rs46270608	snp	A/C/G			intron-variant	Trim30d	GRCm38.p3	7:104489086	AGGAAGGACAGCCTC[A/C/G]AGTCAGATATCTTGA	209387
rs46315748	snp	C/T			intron-variant	Trim30d	Mm_Celera	7:104494411	TAATTCCACCTCTAA[C/T]AACAAAAATAACAGG	209387
rs46334794	snp	A/G			intron-variant	Trim30d	Mm_Celera	7:104494704	AAAAAAATAAGGAAG[A/G]ACATTCCATACTGGT	209387
rs46382792	snp	C/G			upstream-variant-2KB	Trim30d	Mm_Celera	7:104508243	ACTCTTACAGAATGA[C/G]AACAGGAAGGAAGTT	209387
rs46407918	snp	A/G			intron-variant	Trim30d	Mm_Celera	7:104505659	ATAGGAGAGAGATGA[A/G]TAGGGAAACTGAAGG	209387
rs46472239	snp	A/G			intron-variant	Trim30d	Mm_Celera	7:104504637	TAGAAGAGAAAGTGG[A/G]CAATAATCTTGAACA	209387
rs46477723	snp	A/G			intron-variant	Trim30d	Mm_Celera	7:104497329	CAATAAAAGAATTTC[A/G]GAAAGGATCGATCTG	209387

Full records

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