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
rs3654432	snp	C/T	0.444444	0.157135	intron-variant	Itsn1	GRCm38.p3	16:91782731	TGCTCTTAGGTGGTG[C/T]GCCCCTCCGCATGTT	16443
rs3654484	snp	C/G	0.5	0	intron-variant	Itsn1	Mm_Celera	16:91782757	ATGTTGCTTGCATGG[C/G]CTTGATGGATCATGT	16443
rs3654487	snp	A/G	0.5	0	intron-variant	Itsn1	Mm_Celera	16:91782761	TGCTTGCATGGGCTT[A/G]ATGGATCATGTTGTG	16443
rs3655085	snp	C/G	0.359862	0.224567	intron-variant	Itsn1	Mm_Celera	16:91782809	TTTGAAGCACGCCAT[C/G]TTTGCTGTTTGAAAG	16443
rs3671778	snp	A/G	0.277778	0.248452	intron-variant	Itsn1	GRCm38.p3	16:91837009	GCATCCTCGTGAACA[A/G]TTCAGTGTCCATCTG	16443
rs3684385	snp	A/T	0.444444	0.157135	intron-variant	Itsn1	GRCm38.p3	16:91833874	GAAGTGATTTATCCC[A/T]CTTGGACATAGGGAA	16443
rs3687287	snp	G/T	0.396694	0.202437	intron-variant	Itsn1	Mm_Celera	16:91837229	CTGTGGCATTCATTC[G/T]CCCTGTTCTCAGACG	16443
rs3692607	snp	C/T	0.385633	0.210009	intron-variant	Itsn1	Mm_Celera	16:91774923	CCAAAAATCAGTTGG[C/T]AAACAGGTATGGCTG	16443
rs3693923	snp	C/T	0.46875	0.121031	intron-variant	Itsn1	GRCm38.p3	16:91902296	TAATTGTTTTAACCT[C/T]CCTTCTAGCCCACCA	16443
rs3695773	snp	A/G	0.46875	0.121031	intron-variant	Itsn1	GRCm38.p3	16:91902613	TGATCAGGGAAGAAG[A/G]CAAGGAGAACCAATG	16443
rs3712349	snp	A/G	0.5	0	intron-variant	Itsn1	GRCm38.p3	16:91897673	TATTTGCTGTGTGGA[A/G]TTTTGCCTGCATGTG	16443
rs3712364	snp	C/T	0.5	0	intron-variant	Itsn1	GRCm38.p3	16:91897679	CTGTGTGGAATTTTG[C/T]CTGCATGTGTGTCTG	16443
rs3713005	snp	C/T	0.5	0	intron-variant	Itsn1	Mm_Celera	16:91897777	GAGCCCACATGTGAG[C/T]ACTGGGAACCCAGGG	16443
rs3713023	snp	C/T	0.5	0	intron-variant	Itsn1	GRCm38.p3	16:91897779	GCCCACATGTGAGTA[C/T]TGGGAACCCAGGGCT	16443
rs3713211	snp	C/T	0.5	0	intron-variant	Itsn1	Mm_Celera	16:91782615	TTTAGGTATAAATTA[C/T]AGCTATAAAATTTAC	16443
rs3713261	snp	C/T	0.359862	0.224567	intron-variant	Itsn1	Mm_Celera	16:91782641	TTTACCTTATGTCCA[C/T]GTAGGCTTTAGGCAA	16443
rs3718712	snp	A/G	0.5	0	intron-variant	Itsn1	Mm_Celera	16:91786299	CCCCAGGAAGGTAGG[A/G]CTTAGCATCAGAGAT	16443
rs3719314	snp	C/T	0.207612	0.24638	intron-variant	Itsn1	Mm_Celera	16:91786374	TGAGTGACCAACACA[C/T]GGACACCGGAAAGGC	16443
rs4138168	snp	A/T	0.5	0	intron-variant	Itsn1	Mm_Celera	16:91786586	TAACGTCCGAGTCCC[A/T]TGCTGGACTGGGCTG	16443
rs4138387	snp	A/G	0.5	0	intron-variant	Itsn1	Mm_Celera	16:91897516	ATACTCCAGAAGAGG[A/G]CATCAGATTTCGTTA	16443
rs4219320	snp	A/G	0.375	0.216506	upstream-variant-2KB, intron-variant	Itsn1, Cryzl1	Mm_Celera	16:91727644	CTGGATTCGGAGAGC[A/G]GCGAATAGCCACAGG	16443
rs4219321	snp	A/G	0.48	0.0979796	upstream-variant-2KB, intron-variant	Itsn1, Cryzl1	Mm_Celera	16:91728441	CAGGGCATCTCTGAG[A/G]TCGGCGTGTGATGCG	16443
rs4219322	snp	A/T	0.444444	0.157135	upstream-variant-2KB	Itsn1, Cryzl1	Mm_Celera	16:91729341	GAGGGAGATGAGGAG[A/T]TAGGCGGGAGTGAGG	16443
rs4219323	snp	A/G	0.375	0.216506	intron-variant, upstream-variant-2KB, utr-variant-5-prime	Itsn1, Cryzl1	Mm_Celera	16:91730288	AGCAAGGAGGAGCTG[A/G]CTGGATCTCCCTTCA	16443
rs4219324	snp	C/T	0.5	0	intron-variant	Itsn1	Mm_Celera	16:91731609	CCACATCCATCCTTC[C/T]TTCCTTCCTTTTTTC	16443
rs4219325	snp	A/G	0.48	0.0979796	intron-variant	Itsn1	Mm_Celera	16:91732585	ATTTTATAAATGATG[A/G]TAATCCCAACATAAA	16443
rs4219326	snp	A/G	0.375	0.216506	intron-variant	Itsn1	GRCm38.p3	16:91734444	ACAGCTCTAGTTTCA[A/G]CAGTAGACTATCTCA	16443
rs4219327	snp	A/G	0.375	0.216506	intron-variant	Itsn1	GRCm38.p3	16:91734513	CTCAATGCCAGCCAC[A/G]TACACCCACTCGAGC	16443
rs4219328	snp	C/T	0.375	0.216506	intron-variant	Itsn1	Mm_Celera	16:91734766	AGCTTTCACCGATGT[C/T]TTTCTTTGTTGGTGG	16443
rs4219329	snp	C/T	0.375	0.216506	intron-variant	Itsn1	GRCm38.p3	16:91737296	TCTCCATGTCCCAGA[C/T]AGTCCACCACACGGA	16443
rs4219330	snp	A/G	0.375	0.216506	intron-variant	Itsn1	Mm_Celera	16:91737512	TTGAAGGAGAACAAG[A/G]GAAATACTGGATCAG	16443
rs4219331	snp	C/G	0.375	0.216506	intron-variant	Itsn1	GRCm38.p3	16:91738711	GCCTGGGAGACTGAA[C/G]ACCTGTTGTCTGTGG	16443
rs4219332	snp	C/G	0.345679	0.230967	intron-variant	Itsn1	GRCm38.p3	16:91743273	ACAGAGCGTTGTTGA[C/G]AAACTCCCTCTCCTA	16443
rs4219333	snp	C/G	0.5	0	intron-variant, upstream-variant-2KB	Itsn1	Mm_Celera	16:91746216	GGAGTGTCAGTGTTC[C/G]ACAAAGCAAGCAGAA	16443
rs4219334	snp	C/T	0.444444	0.157135	intron-variant	Itsn1	Mm_Celera	16:91750687	TGGACAAGAGAGCTT[C/T]ATCCTTCTACCCTAT	16443
rs4219335	snp	A/G	0.5	0	intron-variant	Itsn1	Mm_Celera	16:91751773	CTTGAAAAAGTGGCC[A/G]GGCCATTCAAAGCCT	16443
rs4219336	snp	C/T	0.432133	0.171253	intron-variant	Itsn1	Mm_Celera	16:91752703	TGAGGTATGATGCTG[C/T]TTCTCTGTGCTTTTG	16443
rs4219337	snp	A/G	0.444444	0.157135	intron-variant	Itsn1	Mm_Celera	16:91758563	TTTATTTTATCTTTT[A/G]AGGCAAGGATTCAGT	16443
rs4219338	snp	C/T	0.408163	0.193609	intron-variant	Itsn1	GRCm38.p3	16:91758995	AGATCAGGCTGGCCT[C/T]GAACTCAGAAATCCG	16443
rs4219339	snp	A/G	0.408163	0.193609	intron-variant	Itsn1	GRCm38.p3	16:91759036	CCTCCCAAGTGCTGG[A/G]ATTACAGGCGTGTGC	16443
rs4219340	snp	C/T	0.375	0.216506	intron-variant	Itsn1	Mm_Celera	16:91760432	CAAGGTATGTGTTCC[C/T]TTAAGCAGTAGGGTC	16443
rs4219341	snp	A/C	0.48	0.0979796	intron-variant	Itsn1	Mm_Celera	16:91760468	CTGTTAACTCTGATG[A/C]ACCGGAGAATTAGGT	16443
rs4219342	snp	C/T	0.48	0.0979796	intron-variant	Itsn1	GRCm38.p3	16:91760650	TCAGTGTTGTAAGTC[C/T]TCCAGTGAGGCTGCG	16443
rs4219343	snp	A/G	0.48	0.0979796	intron-variant	Itsn1	Mm_Celera	16:91760834	CCACACTGGAACTGG[A/G]GCTTTTGTTTAGTCA	16443
rs4219344	snp	A/T	0.277778	0.248452	intron-variant	Itsn1	Mm_Celera	16:91761081	GTATTAAGCTCTATT[A/T]GAAGCCAAAATTGAG	16443
rs4219345	snp	A/T	0.297521	0.245442	intron-variant	Itsn1	Mm_Celera	16:91761884	TCAGGCGAGTGTGTC[A/T]CTGTATGTCCAGCCT	16443
rs4219346	snp	C/T	0.408163	0.193609	intron-variant	Itsn1	Mm_Celera	16:91762695	GTCTGATTCCATTTG[C/T]TTGTTGTCTGGCCAT	16443
rs4219347	snp	A/G	0.287335	0.247197	intron-variant	Itsn1	Mm_Celera	16:91763311	GTAATCGAGACAGTT[A/G]CCCGTGGCTTCTAGA	16443
rs4219348	snp	A/G	0.375	0.216506	intron-variant	Itsn1	Mm_Celera	16:91763384	AGGCATCCTTGACAG[A/G]CACCCTGTTTTTTCA	16443
rs4219349	snp	C/T	0.287335	0.247197	intron-variant	Itsn1	Mm_Celera	16:91763560	TAGATCGAGAGGAAC[C/T]TTTCACCTTGTGACT	16443
rs4219350	snp	C/T	0.396694	0.202437	intron-variant	Itsn1	Mm_Celera	16:91764052	GCCACATGGCTCACT[C/T]AGGACTTTATTCAGC	16443
rs4219351	snp	C/T	0.408163	0.193609	intron-variant	Itsn1	Mm_Celera	16:91764403	GCTTTTTTTTCTTTT[C/T]CCATATATTTTTGCT	16443
rs4219352	snp	G/T	0.375	0.216506	intron-variant	Itsn1	Mm_Celera	16:91766737	ACTTATGTTCTTTAT[G/T]CGAGGCGTGGGGCTG	16443
rs4219353	snp	A/G	0.433884	0.169371	intron-variant	Itsn1	GRCm38.p3	16:91766792	TTGACACTGATTGAA[A/G]TCCGGGCACACAGGG	16443
rs4219354	snp	A/C	0.297521	0.245442	intron-variant	Itsn1	Mm_Celera	16:91766819	AGGGCTAACAGTGTG[A/C]CCCACCTCGCTGCCC	16443
rs4219355	snp	A/G	0.362812	0.2231	intron-variant	Itsn1	Mm_Celera	16:91766972	CTCTTGGTTTATGTA[A/G]TGACATGGAAGCAGA	16443
rs4219356	snp	A/G	0.30839	0.243086	intron-variant	Itsn1	GRCm38.p3	16:91767135	GATTATGTGGCGGAC[A/G]TAACCTATTCTATGA	16443
rs4219357	snp	C/T	0.375	0.216506	intron-variant	Itsn1	GRCm38.p3	16:91767412	ACTCTGCCCCCCACA[C/T]ATGTGCTGAAGCCCG	16443
rs4219358	snp	C/T	0.375	0.216506	intron-variant	Itsn1	Mm_Celera	16:91767494	GTAATGACACCATGG[C/T]GACTGTCAATTGACA	16443
rs4219359	snp	C/T	0.375	0.216506	intron-variant	Itsn1	Mm_Celera	16:91767779	GATTCCTCAGTAAAG[C/T]TTCCCTCCCTCTGAC	16443
rs4219360	snp	A/G	0.375	0.216506	intron-variant	Itsn1	GRCm38.p3	16:91770208	CATGGTGTCTTCTGT[A/G]CTATACCTGAGCAGG	16443
rs4219361	snp	A/G	0.375	0.216506	intron-variant	Itsn1	GRCm38.p3	16:91770211	GGTGTCTTCTGTGCT[A/G]TACCTGAGCAGGGAC	16443
rs4219362	snp	C/T	0.35124	0.228584	intron-variant	Itsn1	Mm_Celera	16:91770482	GAGACTGTCAAGATC[C/T]ACTTTCTCCTGAGCA	16443
rs4219363	snp	A/G	0.42344	0.180051	intron-variant	Itsn1	GRCm38.p3	16:91770985	GCCACGTGACTAGAC[A/G]GCATTGATCAGGATG	16443
rs4219364	snp	A/G	0.444444	0.157135	intron-variant	Itsn1	Mm_Celera	16:91771174	GTTTCTCACTTACTG[A/G]GCAGGGTACAGTCAC	16443
rs4219365	snp	C/T	0.444444	0.157135	intron-variant	Itsn1	Mm_Celera	16:91771183	TTACTGAGCAGGGTA[C/T]AGTCACCTCTGTTTC	16443
rs4219366	snp	A/G	0.46875	0.121031	intron-variant	Itsn1	GRCm38.p3	16:91771484	GCCTCCCCATTCCAG[A/G]CTCTGTTGTTTGCCT	16443
rs4219367	snp	A/C	0.46875	0.121031	intron-variant	Itsn1	GRCm38.p3	16:91771530	AGTAGTAGGGCCCTG[A/C]GTCCCTTGCCCTTCC	16443
rs4219368	snp	C/T	0.5	0	intron-variant	Itsn1	Mm_Celera	16:91771886	TGTGGGTGTAGATTT[C/T]GATGATGTTTGATAG	16443
rs4219369	snp	C/T	0.5	0	intron-variant	Itsn1	Mm_Celera	16:91772042	ATAGTCATGTTACCC[C/T]CTGGCACATCTGGCC	16443
rs4219370	snp	G/T	0.471655	0.115624	intron-variant	Itsn1	GRCm38.p3	16:91772139	CTGTTTGCCCTCAAT[G/T]TTTCATTAATGCAAA	16443
rs4219371	snp	C/T	0.48	0.0979796	intron-variant	Itsn1	Mm_Celera	16:91772311	GACCCATAACCTCAG[C/T]CTCTTATCATTTCTT	16443
rs4219372	snp	A/T	0.48	0.0979796	intron-variant	Itsn1	GRCm38.p3	16:91772509	AATTGATTGCTTTTT[A/T]AAAAAAGATCCCCTA	16443
rs4219373	snp	A/T	0.48	0.0979796	intron-variant	Itsn1	Mm_Celera	16:91772510	ATTGATTGCTTTTTA[A/T]AAAAAGATCCCCTAA	16443
rs4219374	snp	C/T	0.375	0.216506	intron-variant	Itsn1	GRCm38.p3	16:91772649	AGCTCAGTGGATGAG[C/T]GCTTCGCTGGCTTGC	16443
rs4219375	snp	A/C	0.42	0.183303	intron-variant	Itsn1	GRCm38.p3	16:91772751	GGAGAGCGTGTGCTT[A/C]CTTGGTGTGAACCCG	16443
rs4219376	snp	A/G	0.408163	0.193609	intron-variant	Itsn1	GRCm38.p3	16:91772837	GACGATAGTGGTGCC[A/G]AGCTTCCTTGTGCAT	16443
rs4219377	snp	A/G	0.244898	0.249948	intron-variant	Itsn1	Mm_Celera	16:91772953	GAAAGCTTAATATGT[A/G]TTCACAATCTACTTT	16443
rs4219378	snp	A/G	0.48	0.0979796	intron-variant	Itsn1	Mm_Celera	16:91776583	ATTTAATGATGTTGC[A/G]TCATATTTCTAGCTA	16443
rs4219379	snp	A/C	0.413194	0.189387	intron-variant	Itsn1	Mm_Celera	16:91776612	TATGCTGCTGTGCAG[A/C]AATTTCCATTCTTTT	16443
rs4219380	snp	G/T	0.48	0.0979796	intron-variant	Itsn1	Mm_Celera	16:91776898	CCAGAGTATGGAGCG[G/T]CTGGTCACTGGATGT	16443
rs4219381	snp	C/T	0.244898	0.249948	intron-variant	Itsn1	Mm_Celera	16:91777228	CTTAGTTCCCTGTGT[C/T]TAGTCGGGCTTTATT	16443
rs4219382	snp	C/T	0.48	0.0979796	intron-variant	Itsn1	Mm_Celera	16:91778609	CTGACTATAACTTAA[C/T]TGAGGGCACCTCAGT	16443
rs4219383	snp	C/T	0.244898	0.249948	intron-variant	Itsn1	Mm_Celera	16:91778838	CATGATACCTAGCTG[C/T]AGGGCTGGTGAGATG	16443
rs4219384	snp	C/T	0.444444	0.157135	intron-variant	Itsn1	Mm_Celera	16:91778873	AGCAGTTAGGAGTGC[C/T]GACTGCTTTTCCTAA	16443
rs4219385	snp	C/T	0.444444	0.157135	intron-variant	Itsn1	GRCm38.p3	16:91778881	GGAGTGCCGACTGCT[C/T]TTCCTAAGGTCCTGA	16443
rs4219386	snp	C/T	0.408163	0.193609	intron-variant	Itsn1	Mm_Celera	16:91779545	GGTTAATAATTTGCC[C/T]TTGCTTTGCAGTAAA	16443
rs4219387	snp	G/T	0.444444	0.157135	intron-variant	Itsn1	Mm_Celera	16:91779719	GGGTGAGAGAACACA[G/T]GCTAAAAGCTGCTGG	16443
rs4219388	snp	A/G	0.244898	0.249948	intron-variant	Itsn1	Mm_Celera	16:91779753	AAGATGACACGTGCA[A/G]GTACGCCGGGAAGAG	16443
rs4219389	snp	A/G	0.444444	0.157135	intron-variant	Itsn1	GRCm38.p3	16:91779841	TTTCTTGCCTTAATC[A/G]GAATCAGCGTGTCAC	16443
rs4219390	snp	C/T	0.387812	0.208586	intron-variant	Itsn1	Mm_Celera	16:91780160	ACGTTCTGTGTAGGG[C/T]CCTTACCACAGTCTA	16443
rs4219391	snp	A/G	0.444444	0.157135	intron-variant	Itsn1	Mm_Celera	16:91780187	TCTAAGGCAGCATGA[A/G]GGTGGATGGTGCCAC	16443
rs4219392	snp	A/C	0.375	0.216506	intron-variant	Itsn1	GRCm38.p3	16:91780713	TTCCTCTTTCTATGT[A/C]TGTGCTGGTCTTAGG	16443
rs4219393	snp	A/G	0.4032	0.19756	intron-variant	Itsn1	Mm_Celera	16:91783288	CTTCACCTTTTCAGC[A/G]AGCGCTGCTGGTCTA	16443
rs4219394	snp	C/T	0.48	0.0979796	intron-variant	Itsn1	Mm_Celera	16:91783458	GTGAAACATGGCCAT[C/T]GGATGTTCCCACCTC	16443
rs4219395	snp	G/T	0.32	0.24	intron-variant	Itsn1	Mm_Celera	16:91783507	TCACAGAGTGTTTTG[G/T]CCATCACCTCGGATT	16443
rs4219396	snp	C/T	0.244898	0.249948	intron-variant	Itsn1	Mm_Celera	16:91784192	TACATTCCTACCGAG[C/T]GGCAGGAAATCCGTT	16443
rs4219397	snp	G/T	0.30839	0.243086	intron-variant	Itsn1	GRCm38.p3	16:91785430	AAGTTTGGTTTCTTC[G/T]GTAGAAAGAGAGCAT	16443
rs4219398	snp	A/G	0.340265	0.233136	intron-variant	Itsn1	GRCm38.p3	16:91785473	TAGGGCAAACATTAA[A/G]TGGCAGTGCAGAAGT	16443
rs4219399	snp	A/G	0.375	0.216506	intron-variant	Itsn1	Mm_Celera	16:91785481	ACATTAAGTGGCAGT[A/G]CAGAAGTTAAATTGT	16443

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