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
rs13469313	snp	A/G	0.32	0.24	utr-variant-3-prime	Rnf14	Mm_Celera	18:38316772	GTTCTACTGATTAAG[A/G]CACATACATTTTCCA	56736
rs31734584	snp	C/T	0.336735	0.234472	missense	Rnf14	Mm_Celera	18:38308091	CTGCTGCGGCGGATG[C/T]AGACCAAGAAGAAAC	56736
rs31734585	snp	A/G	0.152778	0.230321	missense	Rnf14	Mm_Celera	18:38308042	AGGGCAACAGCCCAG[A/G]CCTCTTCCAGCACAG	56736
rs31734586	snp	A/G	0.165289	0.235211	missense	Rnf14	Mm_Celera	18:38308033	GTTCAGAGAAGGGCA[A/G]CAGCCCAGGCCTCTT	56736
rs31734587	snp	C/T	0.132653	0.220748	intron-variant	Rnf14	Mm_Celera	18:38307848	CAAATTCAGCATCCT[C/T]ATGTGCTCTCTCCCA	56736
rs31734588	snp	A/C	0.132653	0.220748	intron-variant	Rnf14	Mm_Celera	18:38307822	CAGGAGCTGGTCTAT[A/C]ATCATCTTTTCAAAT	56736
rs31734589	snp	G/T	0.473373	0.11227	intron-variant	Rnf14	Mm_Celera	18:38307772	AAGTAAGAAAGAAAT[G/T]TCAGGAAGTTATGCT	56736
rs31734590	snp	C/T	0.408163	0.193609	intron-variant	Rnf14	Mm_Celera	18:38307648	CCTGGCTCTGTGTCC[C/T]GTGGCAGCCTCTTGT	56736
rs31734591	snp	A/G	0.336735	0.234472	intron-variant	Rnf14	Mm_Celera	18:38307372	CTGTTAGATAGATTT[A/G]TTATAGGAAGTACAG	56736
rs31734592	snp	A/G	0.244898	0.249948	intron-variant	Rnf14	Mm_Celera	18:38307269	TTGAGCTGTGTTCCC[A/G]GTTTTGAATGATTCT	56736
rs31734593	snp	A/G	0.426035	0.177515	intron-variant	Rnf14	Mm_Celera	18:38306904	ACTGTTACCAGAAAG[A/G]AAAAAAAGCAGAGCA	56736
rs31735314	snp	C/T	0.244898	0.249948	intron-variant	Rnf14	Mm_Celera	18:38306406	AATTGTCAGGTATTA[C/T]CCTGTGTGTATTAAA	56736
rs31735315	snp	A/G	0.375	0.216506	intron-variant	Rnf14	Mm_Celera	18:38305858	CGCTTAAGCCGGTAT[A/G]CTTAAAGGTATTATA	56736
rs31735316	snp	A/G	0.152778	0.230321	intron-variant	Rnf14	Mm_Celera	18:38305033	GGCCTGGAGGTGTGC[A/G]CTGGGATATTAGTTT	56736
rs31735317	snp	A/G	0.260355	0.249785	intron-variant	Rnf14	Mm_Celera	18:38304893	TGAACAGTATTTTCA[A/G]TTTAACAATTTTAAA	56736
rs31735318	snp	C/T	0.132653	0.220748	intron-variant	Rnf14	Mm_Celera	18:38304767	TGAGTGCTAGACTGC[C/T]TCTTGCCAAGCAGGG	56736
rs31735319	snp	C/T	0.124444	0.216185	intron-variant	Rnf14	Mm_Celera	18:38304700	CTGCTTCCCTCTGCT[C/T]CAGACCACTGCGTAA	56736
rs31735320	snp	G/T	0.444444	0.157135	intron-variant	Rnf14	Mm_Celera	18:38304591	TTTTAGATGGAAAAG[G/T]TAAAACAGTTTAACT	56736
rs31735321	snp	A/G	0.260355	0.249785	intron-variant	Rnf14	Mm_Celera	18:38303072	GAAAAGGATACTGTA[A/G]TAACTAGCCAGAAGC	56736
rs31735322	snp	A/C	0.132653	0.220748	intron-variant	Rnf14	Mm_Celera	18:38302689	CAGTGTTCTGAGATG[A/C]GATAGATCAATAGCT	56736
rs31735323	snp	A/G	0.336735	0.234472	intron-variant	Rnf14	Mm_Celera	18:38301859	GAAACTTTTAACATC[A/G]TCTTTAATTGAAGAC	56736
rs31736304	snp	A/G	0.336735	0.234472	intron-variant	Rnf14	Mm_Celera	18:38301525	GACTAGGAACTTAAC[A/G]TAAGGGATGGACGGT	56736
rs31736305	snp	A/G	0.336735	0.234472	intron-variant	Rnf14	Mm_Celera	18:38301443	CTTTATACATCACAC[A/G]GCACCTAAGTAGATT	56736
rs31736306	snp	A/G	0.152778	0.230321	intron-variant	Rnf14	Mm_Celera	18:38301185	TTAGATGAGCCTGTG[A/G]CTGTGTTGTGTGCCG	56736
rs31736307	snp	A/G	0.244898	0.249948	intron-variant	Rnf14	Mm_Celera	18:38301165	TCTCTAGAAGCTGAG[A/G]TCACTTAGATGAGCC	56736
rs31736308	snp	C/G	0.244898	0.249948	intron-variant	Rnf14	Mm_Celera	18:38300995	CATGGTTGATTTCTG[C/G]TTGATTTCTAGAATC	56736
rs31736309	snp	A/T	0.244898	0.249948	intron-variant	Rnf14	Mm_Celera	18:38300895	TAGTAGTTGATCAGT[A/T]CAGCTGTTGATTATC	56736
rs31736310	snp	A/G	0.165289	0.235211	intron-variant	Rnf14	Mm_Celera	18:38300837	TTTTTTGGCCATTGA[A/G]TTGAGATATATCCTG	56736
rs31736311	snp	C/T	0.132653	0.220748	intron-variant	Rnf14	Mm_Celera	18:38300751	TAAGTATTAGTGACA[C/T]AGATTTAGTGTATTT	56736
rs31736312	snp	G/T	0.165289	0.235211	utr-variant-5-prime, intron-variant	Rnf14	Mm_Celera	18:38299782	TGTAGTATATCGGAC[G/T]CAAATCTCACATCTT	56736
rs31736313	snp	A/G	0.18	0.24	intron-variant	Rnf14	Mm_Celera	18:38298532	GAAGCTGAACCCATG[A/G]TTGTTTTAAGATGTT	56736
rs31737214	snp	A/G	0.18	0.24	upstream-variant-2KB	Rnf14	Mm_Celera	18:38296534	ATTTGAGGGTTTGAA[A/G]CTTGCACATTCTGTA	56736
rs31737215	snp	A/C	0.197531	0.244432	upstream-variant-2KB	Rnf14	Mm_Celera	18:38296331	ATGCAGCAGTTAAAA[A/C]ATGCAGTGAGTTAAT	56736
rs31737216	snp	A/G	0.244898	0.249948	upstream-variant-2KB	Rnf14	Mm_Celera	18:38295619	TCTTTCTCTTTTAGT[A/G]TGCAGCAGTCTGTGT	56736
rs31737217	snp	C/T	0.277778	0.248452	upstream-variant-2KB	Rnf14	Mm_Celera	18:38295589	TCTTAGAAAAATTGT[C/T]GAAGCAGGCATTTTT	56736
rs31737764	snp	G/T	0.473373	0.11227	downstream-variant-500B	Rnf14	Mm_Celera	18:38318129	TTTATATCATCACTG[G/T]AGTTAAAAAAAAGAT	56736
rs31737765	snp	A/C/G	0.35503	0.226867	downstream-variant-500B	Rnf14	GRCm38.p3	18:38318095	AACATGCTCATTTCA[A/C/G]GGGCTTTCATCCACA	56736
rs31737766	snp	C/G	0.260355	0.249785	downstream-variant-500B	Rnf14	Mm_Celera	18:38318025	AGTGACACACACGCA[C/G]ACATTTAAAGAGAAA	56736
rs31737767	snp	C/T	0.489796	0.070696	downstream-variant-500B	Rnf14	Mm_Celera	18:38317994	CTCAGGTGTGCTGAG[C/T]CTGAGTCTGCCACTA	56736
rs31737768	snp	C/T	0.489796	0.070696	utr-variant-3-prime	Rnf14	Mm_Celera	18:38317474	TGAAGAGCATCATGG[C/T]TCTACCCTGACCTTC	56736
rs31737769	snp	A/G	0.297521	0.245442	utr-variant-3-prime	Rnf14	Mm_Celera	18:38317421	CACTAGAGTAGGAAA[A/G]AGCCCAGTGTATTCC	56736
rs31737770	snp	A/T	0.489796	0.070696	utr-variant-3-prime	Rnf14	Mm_Celera	18:38317289	AGAATTCCTCCAGAT[A/T]CAGAGTCAGAGCTGT	56736
rs31737771	snp	A/C	0.375	0.216506	utr-variant-3-prime	Rnf14	Mm_Celera	18:38317276	AGGATTCTGGCTCAG[A/C]ATTCCTCCAGATACA	56736
rs31737772	snp	A/G	0.165289	0.235211	utr-variant-3-prime	Rnf14	Mm_Celera	18:38317190	ATTTTTAGTGCCACA[A/G]TCCTTGTGGGTCACT	56736
rs31737773	snp	C/G	0.277778	0.248452	utr-variant-3-prime	Rnf14	Mm_Celera	18:38317087	CATCCGTGCTGTGGA[C/G]GAGCCTGTGCTCTGT	56736
rs31738664	snp	A/G	0.18	0.24	utr-variant-3-prime	Rnf14	Mm_Celera	18:38317011	CCTCAGCTGGGGACA[A/G]TCACAGCCCCAGCCA	56736
rs31738665	snp	A/T	0.391111	0.206368	intron-variant	Rnf14	Mm_Celera	18:38316503	TGCCTAAGTGTATGT[A/T]TGCCTTATGTTATGT	56736
rs31738666	snp	C/T	0.124444	0.216185	intron-variant	Rnf14	Mm_Celera	18:38316386	CTAGATTTTAGCCCT[C/T]CTTAATGAAATGGTT	56736
rs31738667	snp	C/T	0.260355	0.249785	intron-variant	Rnf14	Mm_Celera	18:38315653	GTTGGTGTGCTTGTG[C/T]CATGGTGCACATGTG	56736
rs31738668	snp	A/T	0.489796	0.070696	intron-variant	Rnf14	Mm_Celera	18:38315194	TTTTATCCTCACCTT[A/T]AAAAAATTTATGCTT	56736
rs31738669	snp	A/G	0.391111	0.206368	intron-variant	Rnf14	Mm_Celera	18:38315159	AAAATGGGTTTATAC[A/G]CCTCTTGAAAACAAT	56736
rs31738670	snp	A/G	0.489796	0.070696	intron-variant	Rnf14	Mm_Celera	18:38314852	GTAAAAAACTCGAGT[A/G]TGCCTGCAAGAGGAT	56736
rs31738671	snp	C/T	0.489796	0.070696	intron-variant	Rnf14	Mm_Celera	18:38314662	ATGTTCTTGTCTCTC[C/T]TTCCCACTAGAAATT	56736
rs31738672	snp	C/T	0.124444	0.216185	intron-variant	Rnf14	Mm_Celera	18:38314450	CTGACATGCTTGAGC[C/T]CTGTGACTCCACTTA	56736
rs31738673	snp	A/T	0.231111	0.249285	intron-variant	Rnf14	Mm_Celera	18:38314431	GTATCCTATTTGACC[A/T]CTTCTGACATGCTTG	56736
rs31739674	snp	A/G	0.489796	0.070696	intron-variant	Rnf14	Mm_Celera	18:38314415	ATCATTAAGGAAGGC[A/G]GTATCCTATTTGACC	56736
rs31739675	snp	C/T	0.497778	0.0332592	intron-variant	Rnf14	Mm_Celera	18:38314288	AAATAGACAGTTTTT[C/T]CTTCTTACCAAAAGT	56736
rs31739676	snp	A/G	0.489796	0.070696	intron-variant	Rnf14	Mm_Celera	18:38314251	TCAGGAAGTAGAAGC[A/G]TTTTCTGTATTACTC	56736
rs31739677	snp	G/T	0.5	0	intron-variant	Rnf14	Mm_Celera	18:38313833	CTTCTCCAAGGGCCT[G/T]GCTTCTAGATGCAAC	56736
rs31739678	snp	C/T	0.48	0.0979796	intron-variant	Rnf14	Mm_Celera	18:38313806	CCAATGACTGCCTTA[C/T]CTCACCCTCATCTTC	56736
rs31739679	snp	A/G	0.35503	0.226867	intron-variant	Rnf14	Mm_Celera	18:38313727	TGCAGAGCATTGAGT[A/G]GTGGGAAGTGTAGTT	56736
rs31739680	snp	A/G	0.489796	0.070696	intron-variant	Rnf14	Mm_Celera	18:38313711	TTCTGTCCTGAGACT[A/G]TGCAGAGCATTGAGT	56736
rs31739681	snp	C/G	0.124444	0.216185	intron-variant	Rnf14	Mm_Celera	18:38313689	AGTTTATTTTGGATC[C/G]ATCTGGTTCTGTCCT	56736
rs31739682	snp	C/T	0.489796	0.070696	intron-variant	Rnf14	Mm_Celera	18:38313652	CTTTTGTTAATAAGA[C/T]CACAGGCTAGGTTAG	56736
rs31739683	snp	C/T	0.444444	0.157135	intron-variant	Rnf14	Mm_Celera	18:38313609	GTGCCCACCTCAGAA[C/T]TGAATAAATGATGCT	56736
rs31740574	snp	A/G	0.444444	0.157135	intron-variant	Rnf14	Mm_Celera	18:38313495	TCGACCTTCTGACTG[A/G]AAATTGAATTTCAGT	56736
rs31740575	snp	C/T	0.444444	0.157135	intron-variant	Rnf14	Mm_Celera	18:38313392	CCATACAGGTAACCT[C/T]TAGAGCAGACTCGAG	56736
rs31740576	snp	C/T	0.489796	0.070696	synonymous-codon	Rnf14	Mm_Celera	18:38313252	ATACCTACAAGCAGA[C/T]GAAGCTACTAAGAGG	56736
rs31740577	snp	A/C	0.375	0.216506	synonymous-codon	Rnf14	Mm_Celera	18:38313229	AAATTAATAGACTTA[A/C]GAAATGAATACCTAC	56736
rs31740578	snp	A/T	0.396694	0.202437	intron-variant	Rnf14	Mm_Celera	18:38312738	TTGTTGTTTTTCGTT[A/T]TTGTTTTCCAAGACA	56736
rs31740579	snp	A/G	0.244898	0.249948	intron-variant	Rnf14	Mm_Celera	18:38312706	TTATGTACAATAATG[A/G]GTTTTATTATGAATT	56736
rs31740580	snp	A/C	0.426035	0.177515	intron-variant	Rnf14	Mm_Celera	18:38312661	ACATTTTCACATACG[A/C]TATATTTATGGTTCT	56736
rs31740581	snp	C/G	0.124444	0.216185	intron-variant	Rnf14	Mm_Celera	18:38312638	ATTTAAACTACAGAA[C/G]GTTGTTCACATTTTC	56736
rs31740582	snp	A/G	0.124444	0.216185	intron-variant	Rnf14	Mm_Celera	18:38312601	TTTTTTCAGCATGTT[A/G]AAAACTTTATCTAAT	56736
rs31740583	snp	A/T	0.497778	0.0332592	intron-variant	Rnf14	Mm_Celera	18:38312509	TACCTGGTCTAAGTA[A/T]TTTTTTTTTTGGATC	56736
rs31741284	snp	C/G	0.444444	0.157135	intron-variant	Rnf14	Mm_Celera	18:38312363	TTGTTTTGATAAACC[C/G]ATATTGCTAGTTATA	56736
rs31741285	snp	A/G	0.444444	0.157135	intron-variant	Rnf14	Mm_Celera	18:38312287	TGGTGTGGCATTGGG[A/G]ATAGAAGTCAAGGTC	56736
rs31741286	snp	C/G	0.426035	0.177515	intron-variant	Rnf14	Mm_Celera	18:38311868	AGGAAGAGCACCTTC[C/G]GCAAAGCAAGATTTA	56736
rs31741287	snp	A/G	0.132653	0.220748	intron-variant	Rnf14	Mm_Celera	18:38310661	CTTTCATCCTTGGCC[A/G]AGTAAGAAACAGTGA	56736
rs31741288	snp	C/T	0.132653	0.220748	intron-variant	Rnf14	Mm_Celera	18:38310660	TCTTTCATCCTTGGC[C/T]GAGTAAGAAACAGTG	56736
rs31741289	snp	A/G	0.142012	0.225474	intron-variant	Rnf14	Mm_Celera	18:38310505	TGACAGGCAGGTAGA[A/G]AAATTGAAAGTCAGG	56736
rs31741290	snp	G/T	0.375	0.216506	intron-variant	Rnf14	Mm_Celera	18:38310459	TGAAGAGGACAGTAG[G/T]CAAATGGAAAAGAAC	56736
rs31741291	snp	C/T	0.444444	0.157135	intron-variant	Rnf14	Mm_Celera	18:38310440	CCTACCTTTTCTCAG[C/T]TAGTGAAGAGGACAG	56736
rs31741292	snp	A/G	0.260355	0.249785	intron-variant	Rnf14	Mm_Celera	18:38310390	ATGCTCTAGGGAATC[A/G]GGGCCTTTCTGTCAG	56736
rs31741293	snp	C/T	0.132653	0.220748	intron-variant	Rnf14	Mm_Celera	18:38310277	TGCTGCTTCGGCATG[C/T]GTTTCTGTCTCATCA	56736
rs31742134	snp	A/G	0.132653	0.220748	intron-variant	Rnf14	Mm_Celera	18:38309965	CTCTCATTCAGGGTT[A/G]CTTTGTCAGTTACTG	56736
rs31742135	snp	C/T	0.142012	0.225474	intron-variant	Rnf14	Mm_Celera	18:38309865	AGCAGAGGTGCATGC[C/T]GCTTATGACCAACTT	56736
rs31742136	snp	C/T	0.132653	0.220748	intron-variant	Rnf14	Mm_Celera	18:38309803	TACATTTAGAGCTCT[C/T]ACACCTGTAGAGTTT	56736
rs31742137	snp	C/T	0.244898	0.249948	intron-variant	Rnf14	Mm_Celera	18:38309458	TGGGAAATCTTCAGA[C/T]CTATGGTGTTTTATA	56736
rs31742138	snp	C/T	0.132653	0.220748	intron-variant	Rnf14	Mm_Celera	18:38309373	CTTCTGGAATGAGAA[C/T]AGGGTGTGACTTTTG	56736
rs31742139	snp	C/T	0.277778	0.248452	intron-variant	Rnf14	Mm_Celera	18:38308744	GGTGTTTCATTGTGT[C/T]TATTAAGAGTGCTAT	56736
rs31742140	snp	A/G	0.473373	0.11227	intron-variant	Rnf14	Mm_Celera	18:38308728	TTAGATGCAGTCCAC[A/G]GGTGTTTCATTGTGT	56736
rs31742141	snp	A/G	0.132653	0.220748	intron-variant	Rnf14	Mm_Celera	18:38308703	GGTACTCATGGGATG[A/G]ACCGAGTCCTTAGAT	56736
rs31742142	snp	A/G	0.260355	0.249785	synonymous-codon	Rnf14	Mm_Celera	18:38308137	TGTACAGGATGTAGA[A/G]TCATTGTCAAGTCTG	56736
rs46036231	snp	C/T			downstream-variant-500B	Rnf14	Mm_Celera	18:38318102	TCATTTCACGGGCTT[C/T]CATCCACACATTTTA	56736
rs47564559	snp	A/T			downstream-variant-500B	Rnf14	Mm_Celera	18:38318203	TCGGGAGGCAGAGGC[A/T]GGCAGATTTCTGAGT	56736
rs49575277	snp	A/G			downstream-variant-500B	Rnf14	Mm_Celera	18:38318154	AAAGATAAGTGGGCC[A/G]GGCGGTGGTGACACA	56736
rs49850629	snp	C/T			downstream-variant-500B	Rnf14	Mm_Celera	18:38318189	TGTAATCCCAGCACT[C/T]GGGAGGCAGAGGCAG	56736
rs50750160	snp	C/T			downstream-variant-500B	Rnf14	Mm_Celera	18:38318021	ACTAAGTGACACACA[C/T]GCAGACATTTAAAGA	56736
rs52312165	snp	C/G/T			downstream-variant-500B	Rnf14	GRCm38.p3	18:38318285	AGAGAAACCCTGTCT[C/G/T]GAAAAAACAAAACAA	56736

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