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
rs4228977	snp	C/T	0.244898	0.249948	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	Tom1l1, Cox11	GRCm38.p3	11:90646231	GCCAACAGGGAGAGC[C/T]CCAGTGGACCATTTC	71943
rs4228978	snp	A/G	0.21875	0.248039	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	Tom1l1, Cox11	Mm_Celera	11:90646144	GACAATGCCTTGAGA[A/G]TTCAGGAAAATCTTG	71943
rs4228979	snp	G/T	0.21875	0.248039	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	Tom1l1, Cox11	GRCm38.p3	11:90646130	ACTTCAGGAAAATCT[G/T]GTTGTGAGGAAAACT	71943
rs4228980	snp	C/T	0.21875	0.248039	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	Tom1l1, Cox11	Mm_Celera	11:90646124	GGAAAATCTTGTTGT[C/T]AGGAAAACTGCCTAG	71943
rs4228981	snp	A/G	0.21875	0.248039	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	Tom1l1, Cox11	GRCm38.p3	11:90646108	AGGAAAACTGCCTAG[A/G]ACTAGGCCAACTGGT	71943
rs4228982	snp	C/T	0.21875	0.248039	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	Tom1l1, Cox11	GRCm38.p3	11:90645985	ATAAAATATTGTAAA[C/T]AGATGGGGAAAGGAA	71943
rs4228983	snp	C/G	0.21875	0.248039	utr-variant-3-prime, nc-transcript-variant	Tom1l1, Cox11	Mm_Celera	11:90645941	TTTATTTAACTGAAT[C/G]TGAATGTACAATTCA	71943
rs4228984	snp	A/G	0.21875	0.248039	utr-variant-3-prime, nc-transcript-variant	Tom1l1, Cox11	GRCm38.p3	11:90645805	TGTAGTTAGTCCTAT[A/G]TAATGTTTAACATTC	71943
rs4228985	snp	A/T	0.188366	0.242283	utr-variant-3-prime, nc-transcript-variant	Tom1l1, Cox11	Mm_Celera	11:90645797	GTCCTATGTAATGTT[A/T]AACATTCTTGCCTTT	71943
rs6408734	snp	C/T	0.5	0	intron-variant	Tom1l1	Mm_Celera	11:90669268	CCCCAAGAACTACAG[C/T]TCAAACCAATGAGGG	71943
rs6410445	snp	A/G	0.5	0	intron-variant	Tom1l1	Mm_Celera	11:90669582	CGGAGCTTGATAACT[A/G]TTCTCATGAGCATCC	71943
rs6410505	snp	A/T	0.5	0	intron-variant	Tom1l1	Mm_Celera	11:90669625	GAGGTATGGGACATC[A/T]TCGAAAGACTTAGGA	71943
rs13469307	snp	C/T			missense, nc-transcript-variant	Tom1l1	GRCm38.p3	11:90671124	TATTGATGGAGAATA[C/T]TCCTGGCTCTGAAAA	71943
rs13469308	snp	C/G	0.375	0.216506	missense, intron-variant, nc-transcript-variant, upstream-variant-2KB	Tom1l1, LOC105242855	Mm_Celera	11:90672936	TTTTATATTGATAGG[C/G]TGGTCAGATCTCACC	71943
rs13469309	snp	C/T			utr-variant-5-prime, synonymous-codon, nc-transcript-variant	Tom1l1	GRCm38.p3	11:90683262	CTCCAAAAACTATAA[C/T]CACAAAGAAATCCAA	71943
rs13469310	snp	C/T			synonymous-codon, intron-variant, nc-transcript-variant, upstream-variant-2KB	Tom1l1, LOC105242855	Mm_Celera	11:90672893	ATCTGTCCCCACTGC[C/T]CCTGCACTTTCTTCT	71943
rs13481155	snp	A/C/T	0.348188	0.229911	intron-variant	Tom1l1	GRCm38.p3	11:90665277	CGCTCAAGGGTAAGA[A/C/T]GGCGGCCCTTTCTAA	71943
rs26992442	snp	C/G	0.18	0.24	upstream-variant-2KB	Tom1l1	Mm_Celera	11:90688669	TCGGGATCCTACAAT[C/G]TAAAATACGGCATTT	71943
rs26992443	snp	G/T	0.132653	0.220748	upstream-variant-2KB	Tom1l1	Mm_Celera	11:90688339	CCTTTTCCGCGGCAC[G/T]GCTAACATCAGATAC	71943
rs26992444	snp	A/T	0.444444	0.157135	upstream-variant-2KB	Tom1l1	Mm_Celera	11:90688121	CGGGCTTTGTTTTTC[A/T]CCCGTTTCCAAGAGG	71943
rs26992445	snp	A/G	0.142012	0.225474	upstream-variant-2KB	Tom1l1	Mm_Celera	11:90687973	CCTCTCAAGTCACAC[A/G]CCTCCAGAACAATGA	71943
rs26992446	snp	C/T	0.260355	0.249785	intron-variant	Tom1l1	Mm_Celera	11:90687329	ATGAGTGAGCCAAAC[C/T]CAGAAAGGTGGAAAG	71943
rs26992447	snp	G/T	0.132653	0.220748	intron-variant	Tom1l1	Mm_Celera	11:90686594	TGCTTTTCCTAGAGG[G/T]CAGCTCTCTTGCAGT	71943
rs26992448	snp	C/T	0.124444	0.216185	intron-variant	Tom1l1	Mm_Celera	11:90686511	CCTGCGAAGCTTCAG[C/T]GAGGATCCATTTCTG	71943
rs26992449	snp	C/T	0.32	0.24	intron-variant	Tom1l1	Mm_Celera	11:90686500	AGTGCCTTTTGCCTG[C/T]GAAGCTTCAGCGAGG	71943
rs26992450	snp	G/T	0.260355	0.249785	intron-variant	Tom1l1	Mm_Celera	11:90685336	CCTCCTGAACAATTC[G/T]CAGTAACTCAGGAAT	71943
rs26992451	snp	A/C	0.244898	0.249948	intron-variant	Tom1l1	Mm_Celera	11:90684993	ACCCAAACCTTGGCA[A/C]TGGAAACCGAGCTGC	71943
rs27075145	snp	A/T	0.132653	0.220748	intron-variant	Tom1l1	Mm_Celera	11:90683757	GAGATCTGCAAATAG[A/T]GGGTCAAAATTCACT	71943
rs27075146	snp	C/T	0.142012	0.225474	intron-variant	Tom1l1	GRCm38.p3	11:90683725	CTAATTTTGATATGC[C/T]GTAACCTGATGTTAG	71943
rs27075147	snp	A/G	0.21875	0.248039	intron-variant	Tom1l1	Mm_Celera	11:90682926	GTCACACAGTCCAGA[A/G]AGTACTATTATGGGG	71943
rs27075148	snp	C/T	0.132653	0.220748	intron-variant	Tom1l1	Mm_Celera	11:90682782	ATCAATCACGGGTTT[C/T]TAACCACAAACTCAA	71943
rs27075149	snp	A/G	0.132653	0.220748	intron-variant	Tom1l1	Mm_Celera	11:90682735	CTTCAAACATGGCCA[A/G]CGAATACAAACACAT	71943
rs27075150	snp	C/G	0.244898	0.249948	intron-variant	Tom1l1	Mm_Celera	11:90682408	TGATGCTGGCCATGT[C/G]GATGTGAGGTCTTCC	71943
rs27075151	snp	A/G	0.495868	0.0452663	intron-variant	Tom1l1	Mm_Celera	11:90682154	CTATGAGTTATAGAC[A/G]GACAAGAGTCCAGCA	71943
rs27075152	snp	A/C	0.124444	0.216185	intron-variant	Tom1l1	Mm_Celera	11:90681735	CTGATAAGACATTCA[A/C]CTCCTGGTGGTAAGA	71943
rs27075153	snp	C/T	0.124444	0.216185	intron-variant	Tom1l1	Mm_Celera	11:90680961	AAGCCTGCTCTGGAA[C/T]GCATACCAATGACCA	71943
rs27075154	snp	C/T	0.132653	0.220748	intron-variant	Tom1l1	Mm_Celera	11:90680694	ACCTTCCATTAGCCC[C/T]GGAGTCTTCCTGGAC	71943
rs27075155	snp	A/G	0.132653	0.220748	intron-variant	Tom1l1	Mm_Celera	11:90680689	AAAATACCTTCCATT[A/G]GCCCCGGAGTCTTCC	71943
rs27075156	snp	C/G	0.18	0.24	intron-variant	Tom1l1	Mm_Celera	11:90680437	AATACAACCCTCACG[C/G]AGGCAAACCACTAAA	71943
rs27075157	snp	A/G	0.152778	0.230321	intron-variant	Tom1l1	Mm_Celera	11:90680436	TAATACAACCCTCAC[A/G]GAGGCAAACCACTAA	71943
rs27075158	snp	A/T	0.244898	0.249948	intron-variant	Tom1l1	Mm_Celera	11:90680306	ATAAATGGAAGATCC[A/T]CGGGACAACATTCTA	71943
rs27075159	snp	C/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Tom1l1, LOC105242855	Mm_Celera	11:90679219	CTGCTCATAATTCAG[C/T]TTAGCCTCAGAGAAT	71943
rs27075160	snp	A/G	0.277778	0.248452	intron-variant, nc-transcript-variant	Tom1l1, LOC105242855	Mm_Celera	11:90678780	GGCTCTCTAGCTTAG[A/G]GCAATAAAGCTTAGT	71943
rs27075161	snp	C/T	0.493827	0.0552116	intron-variant, nc-transcript-variant	Tom1l1, LOC105242855	Mm_Celera	11:90678547	TACTAGCCTCATGTA[C/T]GAGAGAGCTGTCTTC	71943
rs27075162	snp	A/G	0.48	0.0979796	intron-variant, nc-transcript-variant	Tom1l1, LOC105242855	Mm_Celera	11:90678472	TACTAGATTTCAGAT[A/G]TATCAGAGCTATATC	71943
rs27075163	snp	C/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Tom1l1, LOC105242855	Mm_Celera	11:90678374	AGAGAAATAAAAATT[C/T]GTCACACATGGTTAG	71943
rs27075164	snp	G/T	0.260355	0.249785	intron-variant, nc-transcript-variant	Tom1l1, LOC105242855	Mm_Celera	11:90678330	TGTATTGATGGAGAA[G/T]GTTCTAACACGAGAG	71943
rs27075165	snp	C/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Tom1l1, LOC105242855	Mm_Celera	11:90678212	ATGCCGTCTGCATCA[C/T]GGACACTGGGCCTCT	71943
rs27075166	snp	A/G	0.444444	0.157135	intron-variant, nc-transcript-variant	Tom1l1, LOC105242855	Mm_Celera	11:90678191	CACTTATGTGAACTC[A/G]TGGCAATGCCGTCTG	71943
rs27075167	snp	C/T	0.444444	0.157135	intron-variant, nc-transcript-variant	Tom1l1, LOC105242855	Mm_Celera	11:90677870	TGTCAGAGCTCATTA[C/T]TTCTGTATCATCTCC	71943
rs27090768	snp	C/G	0.244898	0.249948	intron-variant, nc-transcript-variant	Tom1l1, LOC105242855	Mm_Celera	11:90677831	GCAGGCATGCCCTTT[C/G]TGCTTTGCCGCTGGA	71943
rs27090769	snp	C/G	0.459184	0.136902	intron-variant, nc-transcript-variant	Tom1l1, LOC105242855	Mm_Celera	11:90677821	TTGGAGATCAGCAGG[C/G]ATGCCCTTTGTGCTT	71943
rs27090770	snp	C/T	0.197531	0.244432	intron-variant, nc-transcript-variant	Tom1l1, LOC105242855	Mm_Celera	11:90677368	CCTAATGATGCTTTC[C/T]TACAGTTTCCTCATG	71943
rs27090771	snp	A/G	0.486111	0.0821678	intron-variant	Tom1l1	Mm_Celera	11:90666346	AGGCAGAAAGAGGAA[A/G]TACCTAGAAGAAAAC	71943
rs27090772	snp	C/T	0.473373	0.11227	intron-variant	Tom1l1	Mm_Celera	11:90666252	GGAAGGCTGTGGGTG[C/T]AAGGCCAGACAGGTC	71943
rs27090773	snp	A/C	0.46875	0.121031	intron-variant	Tom1l1	Mm_Celera	11:90666128	TACACTTTCAAAATC[A/C]GAGTTCCCTTTCTTC	71943
rs27090774	snp	C/T	0.408163	0.193609	intron-variant	Tom1l1	Mm_Celera	11:90666080	TCAAGATCTTATACT[C/T]CTCCAGTAAGCTAAC	71943
rs27090775	snp	A/G	0.486111	0.0821678	intron-variant	Tom1l1	Mm_Celera	11:90665921	TATTTCTTACAAATG[A/G]TGACAACAATGAGAA	71943
rs27090776	snp	C/T	0.142012	0.225474	intron-variant	Tom1l1	Mm_Celera	11:90665854	TATGCTACCTCATCG[C/T]TAAAGAGAAGGAGAC	71943
rs27090777	snp	A/G	0.260355	0.249785	intron-variant	Tom1l1	Mm_Celera	11:90665820	TGCTCTCCTGCGCAC[A/G]AATTGGCCCCTTTCT	71943
rs27090778	snp	C/T	0.497041	0.0383476	intron-variant	Tom1l1	Mm_Celera	11:90665815	CGTGTTGCTCTCCTG[C/T]GCACGAATTGGCCCC	71943
rs27090779	snp	C/T	0.142012	0.225474	intron-variant	Tom1l1	Mm_Celera	11:90665756	ATTGGTCCAGAGAGA[C/T]ATTTGCTCGGGAGAG	71943
rs27090780	snp	A/G	0.5	0	intron-variant	Tom1l1	Mm_Celera	11:90665680	GAACTATTCAGGCCC[A/G]TAGCAAAGGGCCATA	71943
rs27090781	snp	A/C/T	0.495868	0.0452663	intron-variant	Tom1l1	GRCm38.p3	11:90665629	AAAAGCAGAGGCCTT[A/C/T]GGTGCTACCTTCGGG	71943
rs27090782	snp	C/T	0.152778	0.230321	intron-variant	Tom1l1	Mm_Celera	11:90665439	TTCCATGGGCTGAGC[C/T]TGCTTACTTTCCCCA	71943
rs27090783	snp	A/G	0.165289	0.235211	intron-variant	Tom1l1	Mm_Celera	11:90665278	GCTCAAGGGTAAGAC[A/G]GCGGCCCTTTCTAAC	71943
rs27090784	snp	C/G	0.142012	0.225474	intron-variant	Tom1l1	Mm_Celera	11:90665210	GGGAGCAACTACCCT[C/G]TTAATGACACACATA	71943
rs27090785	snp	C/T	0.18	0.24	intron-variant	Tom1l1	Mm_Celera	11:90665171	ACCAGAATATGATAT[C/T]CCTGAACATGTTAAG	71943
rs27090786	snp	A/G	0.493827	0.0552116	intron-variant	Tom1l1	Mm_Celera	11:90665141	CTGTTACACAAGTTC[A/G]GAGAAGAGCCTAAAA	71943
rs27090787	snp	A/C	0.165289	0.235211	intron-variant	Tom1l1	Mm_Celera	11:90665003	TTGCTCCTCTTTCTG[A/C]CTTGAAGTACTGGAA	71943
rs27090788	snp	A/C/G	0.48	0.0979796	intron-variant	Tom1l1	GRCm38.p3	11:90664771	CCGATAATTACTTGA[A/C/G]TCCTCCAGTACTAAA	71943
rs27090789	snp	A/G	0.152778	0.230321	intron-variant	Tom1l1	Mm_Celera	11:90664730	GGTATTAACTCTTCC[A/G]CGGAGCCCTGATATT	71943
rs27090790	snp	A/C	0.165289	0.235211	intron-variant	Tom1l1	Mm_Celera	11:90664668	TCTCTTTCTCCAAGG[A/C]ACCGGATGGTCTTCC	71943
rs27090791	snp	A/T	0.375	0.216506	intron-variant	Tom1l1	Mm_Celera	11:90664579	TCAAAGCTGAACCTC[A/T]TGCCAGCATAACCCT	71943
rs27090792	snp	C/T	0.297521	0.245442	intron-variant	Tom1l1	Mm_Celera	11:90664562	GGGAAAACTCTCTCG[C/T]TTCAAAGCTGAACCT	71943
rs27090793	snp	C/T	0.152778	0.230321	intron-variant	Tom1l1	Mm_Celera	11:90664560	AAGGGAAAACTCTCT[C/T]GTTTCAAAGCTGAAC	71943
rs27090794	snp	C/T	0.165289	0.235211	intron-variant	Tom1l1	Mm_Celera	11:90664152	AAAGGCTCTGAAGAA[C/T]AACAAGAGGCTCATT	71943
rs27090795	snp	C/T	0.32	0.24	intron-variant	Tom1l1	GRCm38.p3	11:90664069	TCTATCACAGAACCC[C/T]GAAATGTCTCTCTTG	71943
rs27090796	snp	A/G	0.152778	0.230321	intron-variant	Tom1l1	Mm_Celera	11:90664024	CAGATTCAGGGAGTA[A/G]AAAGAGAGGGACAGT	71943
rs27090797	snp	A/T	0.142012	0.225474	intron-variant	Tom1l1	Mm_Celera	11:90663890	TCAGAGGAGGGCCAC[A/T]CCACTTGCAAACAGC	71943
rs27090798	snp	C/T	0.142012	0.225474	intron-variant	Tom1l1	Mm_Celera	11:90663646	GAATATAATGGTGTT[C/T]GGTGCCCGGGACAAA	71943
rs27090799	snp	A/G	0.277778	0.248452	intron-variant	Tom1l1	Mm_Celera	11:90663572	GTTTCCGATGGGACA[A/G]AAACTTTTCCTCTTG	71943
rs27090800	snp	A/T	0.197531	0.244432	intron-variant	Tom1l1	Mm_Celera	11:90663106	CAGTGTCAAGCCAGG[A/T]AAACTGTCCACAGAG	71943
rs27090801	snp	A/G	0.375	0.216506	intron-variant	Tom1l1	Mm_Celera	11:90663105	CCAGTGTCAAGCCAG[A/G]TAAACTGTCCACAGA	71943
rs27090802	snp	A/G	0.375	0.216506	intron-variant	Tom1l1	Mm_Celera	11:90662903	CAAACAGCCTATTCC[A/G]AGACTCCTGACAGGA	71943
rs27090803	snp	A/C	0.297521	0.245442	intron-variant	Tom1l1	Mm_Celera	11:90662788	TCCGCTTTCACAGGG[A/C]GAGCACAAGAACTTG	71943
rs27090804	snp	G/T	0.396694	0.202437	intron-variant	Tom1l1	Mm_Celera	11:90662757	AACAGCAGCAGGCAA[G/T]AAACCAGGGATGTCC	71943
rs27090805	snp	A/G	0.297521	0.245442	intron-variant	Tom1l1	Mm_Celera	11:90662655	CCGATGCCCTGCAAC[A/G]ACTCCCTTCTAGCAA	71943
rs27090806	snp	A/C	0.32	0.24	intron-variant	Tom1l1	Mm_Celera	11:90662652	AAGCCGATGCCCTGC[A/C]ACAACTCCCTTCTAG	71943
rs27090807	snp	C/T	0.142012	0.225474	intron-variant	Tom1l1	Mm_Celera	11:90662608	TTAACAAGCGAGCCA[C/T]AGTGTTTCTGAAATA	71943
rs27090808	snp	C/T	0.152778	0.230321	intron-variant	Tom1l1	Mm_Celera	11:90662412	CACATTCAATATAAA[C/T]TGCACCAGGATTTGA	71943
rs27090809	snp	A/G	0.18	0.24	intron-variant	Tom1l1	Mm_Celera	11:90662347	CAGCACGGGGGCATA[A/G]TTTTACTTCCTGTTA	71943
rs27090810	snp	C/T	0.260355	0.249785	intron-variant	Tom1l1	Mm_Celera	11:90662321	GGGTAGATGTAGTTA[C/T]GGAGCGGTTACAGCA	71943
rs27090811	snp	C/T	0.375	0.216506	intron-variant	Tom1l1	Mm_Celera	11:90662224	TACCTCCAGGGCTGG[C/T]GTGAAAAATCACAGG	71943
rs27090812	snp	A/G	0.142012	0.225474	synonymous-codon, nc-transcript-variant	Tom1l1	Mm_Celera	11:90661770	CCTCTCATATCCAAG[A/G]ACGGCATTATTCAGA	71943
rs27090813	snp	A/G	0.375	0.216506	synonymous-codon, nc-transcript-variant	Tom1l1	GRCm38.p3	11:90661761	TTCTGCTCACCTCTC[A/G]TATCCAAGGACGGCA	71943
rs27090814	snp	C/T	0.444444	0.157135	intron-variant	Tom1l1	GRCm38.p3	11:90661718	AGCATGGTGGTGAAG[C/T]GAGGGCGAGTGGAGG	71943
rs27090815	snp	A/C	0.142012	0.225474	intron-variant	Tom1l1	Mm_Celera	11:90661644	CTATTCACCATGCCA[A/C]CCTACTGAGAGAAAG	71943
rs27090816	snp	C/T	0.277778	0.248452	intron-variant	Tom1l1	Mm_Celera	11:90661217	GGACAAAGTCACAAG[C/T]TTAATCCCAGTGTCA	71943
rs27090817	snp	C/T	0.277778	0.248452	intron-variant	Tom1l1	Mm_Celera	11:90661173	ACAAAAGTATCAGTG[C/T]ATAATTCAGTGACTC	71943

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