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
rs3665749	snp	A/G	0.408163	0.193609	intron-variant	Rnf170	Mm_Celera	8:26128417	TTTCCAAAGGACCAC[A/G]TTCACATGACCAAAA	77733
rs13479658	snp	G/T	0.444444	0.157135	intron-variant	Rnf170	Mm_Celera	8:26138575	AAAGACATGCCAAGT[G/T]TGAGTAAAACCAGTC	77733
rs32599545	snp	C/T	0.375	0.216506	intron-variant	Rnf170	Mm_Celera	8:26138816	ATTTTGTACTACATT[C/T]TACTGTAAGGCAGAA	77733
rs32609227	snp	C/T	0.375	0.216506	intron-variant	Rnf170	Mm_Celera	8:26125566	TCCAGTAAATTATAC[C/T]TTGGTCTCCACACAT	77733
rs32671189	snp	A/G	0.444444	0.157135	intron-variant	Rnf170	Mm_Celera	8:26126626	AGTGGCATGTTGACT[A/G]GTCTTAATCTATACG	77733
rs32671315	snp	A/G	0.5	0	intron-variant	Rnf170	Mm_Celera	8:26139582	GAGCCACTCAGCATG[A/G]GTGCTAGAAACAATA	77733
rs32680725	snp	A/G	0.444444	0.157135	intron-variant	Rnf170	Mm_Celera	8:26121342	GCCTTTAGCTTCACG[A/G]CCACAGGTTTTAGCC	77733
rs32701677	snp	C/T	0.444444	0.157135	intron-variant	Rnf170	Mm_Celera	8:26132054	TGCTCACAAACCTGT[C/T]GTAGGCATTTCTAAT	77733
rs32734759	snp	G/T	0.375	0.216506	downstream-variant-500B	Rnf170	Mm_Celera	8:26143916	TGTTTACTTTAAAAT[G/T]TACAAGTCTTGAAAG	77733
rs32744204	snp	C/T	0.375	0.216506	intron-variant	Rnf170	Mm_Celera	8:26122938	CTTAGCTTGGGTTGT[C/T]TCCTCTCATACTTGC	77733
rs32759300	snp	G/T	0.444444	0.157135	intron-variant	Rnf170	Mm_Celera	8:26139427	GTCCTTTGCTGTTTT[G/T]GACTGAGCATTTAAA	77733
rs32790056	snp	A/T	0.375	0.216506	intron-variant	Rnf170	Mm_Celera	8:26123593	AGAAAAAGTATTTTT[A/T]AAAATTTACTTTAAA	77733
rs32793536	snp	A/C	0.375	0.216506	intron-variant	Rnf170	Mm_Celera	8:26122837	TCGAATATTCCCATC[A/C]TTTCCCTTTGGTTGC	77733
rs32822416	snp	A/G	0.32	0.24	intron-variant	Rnf170	Mm_Celera	8:26128247	TTACATATTTGCGTG[A/G]TTTGGGGTTTTAAGA	77733
rs32824555	snp	A/C	0.444444	0.157135	intron-variant	Rnf170	Mm_Celera	8:26126571	ATGGAGACCACTAGA[A/C]CTCCCAAGTTCTGGA	77733
rs32845167	snp	G/T	0.444444	0.157135	intron-variant	Rnf170	Mm_Celera	8:26125302	ATGCCAGAAGAAGAG[G/T]ATGTCAGCTCTCATT	77733
rs32861280	snp	A/G	0.375	0.216506	intron-variant	Rnf170	Mm_Celera	8:26125399	GTGCTTTAAACCACT[A/G]AACCATCTTTCCAGA	77733
rs32898377	snp	A/C	0.375	0.216506	intron-variant	Rnf170	Mm_Celera	8:26127580	TCAGGCTGGTCTCCA[A/C]CTCATGTAGATCTGC	77733
rs32942255	snp	C/T	0.375	0.216506	intron-variant	Rnf170	Mm_Celera	8:26126243	ATCTCCTGATCTTCC[C/T]GACTCTACCTCGGTC	77733
rs32978425	snp	C/G	0.375	0.216506	intron-variant	Rnf170	Mm_Celera	8:26122922	TAACCTACACGGTTG[C/G]CTTAGCTTGGGTTGT	77733
rs33016145	snp	A/G	0.375	0.216506	intron-variant	Rnf170	Mm_Celera	8:26122917	GTGATTAACCTACAC[A/G]GTTGGCTTAGCTTGG	77733
rs33051065	snp	A/G	0.459184	0.136902	intron-variant	Rnf170	Mm_Celera	8:26139247	CTAGTTTTCCCAGAG[A/G]GCAGAGTTTATCTAT	77733
rs33101903	snp	A/G	0.375	0.216506	intron-variant	Rnf170	Mm_Celera	8:26125580	CCTTGGTCTCCACAC[A/G]TGTGTCATAGCACAC	77733
rs33124787	snp	A/G	0.375	0.216506	intron-variant	Rnf170	Mm_Celera	8:26122800	TAAACCCAGAATCTT[A/G]TTTATACTCTTCCAT	77733
rs33155368	snp	A/G	0.375	0.216506	intron-variant	Rnf170	Mm_Celera	8:26123840	TTTTCACTTCTTCAT[A/G]TTTTAGACCTGTAAT	77733
rs33158861	snp	A/G	0.375	0.216506	intron-variant	Rnf170	GRCm38.p3	8:26123645	GTGGTTTTCCTTAAA[A/G]AAAATAGTATTTTGT	77733
rs33164676	snp	C/T	0.375	0.216506	intron-variant	Rnf170	Mm_Celera	8:26123087	AAGCTGAGCTTCATT[C/T]AGGTTTGGCTAATAG	77733
rs33245776	snp	C/T	0.375	0.216506	intron-variant, upstream-variant-2KB	Rnf170, Hook3	Mm_Celera	8:26120015	TGCTAGGAGTTGGCT[C/T]CATTGAGGTGCATCC	77733
rs33249531	snp	G/T	0.444444	0.157135	intron-variant	Rnf170	Mm_Celera	8:26132441	CTAATGTGCTGAGGA[G/T]GATTGATAACCCAAG	77733
rs33287906	snp	A/C	0.444444	0.157135	intron-variant	Rnf170	Mm_Celera	8:26137211	GCTTACCAAACACTC[A/C]TACCAGCACCTCAAG	77733
rs33315100	snp	A/T	0.375	0.216506	intron-variant	Rnf170	Mm_Celera	8:26125533	TGCCCTGAACCCACA[A/T]GGTAGGAGGGATGCA	77733
rs33347235	snp	A/G	0.32	0.24	intron-variant	Rnf170	Mm_Celera	8:26122164	ACTCCAGAAGAGGGC[A/G]TCAGATCTTGTTACA	77733
rs33356583	snp	G/T	0.444444	0.157135	intron-variant, downstream-variant-500B	Rnf170	Mm_Celera	8:26135790	TAAGATTTTTTTTTT[G/T]TATGTGTGTGTGTGT	77733
rs33395664	snp	A/G	0.444444	0.157135	intron-variant, downstream-variant-500B	Rnf170	Mm_Celera	8:26135792	AGATTTTTTTTTTTT[A/G]TGTGTGTGTGTGTGT	77733
rs33410958	snp	A/G	0.375	0.216506	intron-variant	Rnf170	Mm_Celera	8:26126388	GTAGGGAGTGTGGCC[A/G]CAGACAGGCAGGCGT	77733
rs33474764	snp	C/T	0.375	0.216506	intron-variant	Rnf170	Mm_Celera	8:26123758	GCATGCATTAAGGAG[C/T]GTGCTATGAGTGTCA	77733
rs33522781	snp	C/G	0.444444	0.157135	intron-variant	Rnf170	Mm_Celera	8:26123260	GGTAGCTCTTTATAC[C/G]CTAAGACAGTGAGGG	77733
rs33560738	snp	G/T	0.444444	0.157135	intron-variant	Rnf170	Mm_Celera	8:26124459	GATTGCTTTCCAGAC[G/T]CATTACTGTGATAAA	77733
rs33593586	snp	C/T	0.32	0.24	upstream-variant-2KB, intron-variant	Rnf170, Hook3	Mm_Celera	8:26118535	AAAGGCGAGCAGCAT[C/T]GCTTAACTAGGGGGT	77733
rs36251589	snp	A/G	0.35503	0.226867	intron-variant	Rnf170	Mm_Celera	8:26138359	TATCATTCTTTAGAG[A/G]TTGTTACATTCTTAG	77733
rs36291650	snp	C/G	0.142012	0.225474	intron-variant	Rnf170	Mm_Celera	8:26133661	TAATTGCTGACTTTA[C/G]ACTCGTCATGACATT	77733
rs36397873	snp	A/G	0.35503	0.226867	intron-variant	Rnf170	Mm_Celera	8:26138462	AACCTTTGTTCTATA[A/G]CAGTACCAAAACTTA	77733
rs36399576	snp	A/G	0.277778	0.248452	intron-variant	Rnf170	Mm_Celera	8:26135471	TCTGAAAATTTGGTT[A/G]GATGAGGTAAAATTT	77733
rs36404560	snp	C/T	0.32	0.24	upstream-variant-2KB, intron-variant	Rnf170, Hook3	Mm_Celera	8:26117395	ATCGCCGTTCTCTAT[C/T]TGAAGCATAGCAGTG	77733
rs36408389	snp	A/G	0.231111	0.249285	intron-variant	Rnf170	Mm_Celera	8:26134485	TGTTTCTGCTTTAGA[A/G]TCATAGGCTTTAGAC	77733
rs36413305	snp	C/G	0.132653	0.220748	intron-variant	Rnf170	Mm_Celera	8:26133833	ACAAAGTTCAGTTCA[C/G]GTGCTGTGCTCAGGT	77733
rs36426060	snp	A/T	0.260355	0.249785	intron-variant	Rnf170	Mm_Celera	8:26138553	CTGTAGTGGGATAGA[A/T]AGACTCAAAGACATG	77733
rs36486326	snp	C/T	0.336735	0.234472	intron-variant	Rnf170	Mm_Celera	8:26140054	TAAAGGAAGTCGTAC[C/T]CCAAGATCACTTCAT	77733
rs36490559	snp	A/G	0.142012	0.225474	intron-variant	Rnf170	Mm_Celera	8:26132040	GACAGAAATTTTCCT[A/G]CTCACAAACCTGTTG	77733
rs36534925	snp	A/G	0.260355	0.249785	intron-variant	Rnf170	Mm_Celera	8:26139100	AGATCTGTAAGTAAT[A/G]TTATAGCAGCTACAA	77733
rs36549754	snp	C/T	0.375	0.216506	utr-variant-3-prime, nc-transcript-variant	Rnf170	Mm_Celera	8:26142487	TTTGAATGGACTGAG[C/T]ACTGTAACTGAGCCG	77733
rs36627234	snp	A/G	0.142012	0.225474	intron-variant	Rnf170	Mm_Celera	8:26131281	CTTCCTTAAGAAACA[A/G]TTTCCTTAGAGTCAG	77733
rs36645176	snp	A/C	0.124444	0.216185	intron-variant, upstream-variant-2KB	Hook3, Rnf170	Mm_Celera	8:26117375	GTAGCTCTGTCGTGT[A/C]ACCTATCGCCGTTCT	77733
rs36653537	snp	C/T	0.124444	0.216185	upstream-variant-2KB, intron-variant	Rnf170, Hook3	Mm_Celera	8:26118199	TGACTATTGACAAAA[C/T]CCTGCATGTTTACTT	77733
rs36683662	snp	A/G	0.142012	0.225474	intron-variant	Rnf170	Mm_Celera	8:26134904	TAAGCTAAGCTAAGT[A/G]TTTTATCAAGGAAGC	77733
rs36731835	snp	A/G	0.231111	0.249285	upstream-variant-2KB, intron-variant	Rnf170, Hook3	Mm_Celera	8:26117531	AAAGGTCTCCATTGT[A/G]TAAAGGCTGCTTCAA	77733
rs36789331	snp	C/T	0.142012	0.225474	intron-variant	Rnf170	Mm_Celera	8:26132603	TAACACTACCTGTGT[C/T]GAGAGCTCTTAGCTC	77733
rs36802832	snp	C/T	0.244898	0.249948	intron-variant, downstream-variant-500B	Rnf170	Mm_Celera	8:26136023	TCCAGCCAAATTGCA[C/T]TTTAACCTACTGTGT	77733
rs36813097	snp	A/G	0.124444	0.216185	intron-variant	Rnf170	Mm_Celera	8:26134052	CCTAGAATATGTGAC[A/G]CTCCAGGCAGTGAAA	77733
rs36828354	snp	C/T	0.336735	0.234472	intron-variant	Rnf170	Mm_Celera	8:26133650	CAGGCACGAGGTAAT[C/T]GCTGACTTTAGACTC	77733
rs36907705	snp	A/G	0.142012	0.225474	intron-variant, downstream-variant-500B	Rnf170	Mm_Celera	8:26136126	TGAAATCCTACAGTT[A/G]TAGTGAAAAAACAAG	77733
rs37043743	snp	A/G	0.35503	0.226867	intron-variant	Rnf170	Mm_Celera	8:26140608	TGATACTTTATTGCT[A/G]TTCAGTTGTCTATAA	77733
rs37078915	snp	A/G	0.32	0.24	intron-variant	Rnf170	Mm_Celera	8:26138595	TAAAACCAGTCAGTC[A/G]GGAGTGCCTAAATCT	77733
rs37135686	snp	C/T	0.35503	0.226867	utr-variant-3-prime, nc-transcript-variant	Rnf170	Mm_Celera	8:26141422	ATCCTCAGTGGGTAC[C/T]CATACAAGAATAGAG	77733
rs37215427	snp	C/T	0.142012	0.225474	intron-variant	Rnf170	Mm_Celera	8:26130608	TCCTTTATTAGTGTC[C/T]TCCCTCTTGTGTCTT	77733
rs37261489	snp	A/C	0.132653	0.220748	intron-variant	Rnf170	Mm_Celera	8:26134066	CGCTCCAGGCAGTGA[A/C]AATGTTCCTTCATGT	77733
rs37274536	snp	A/G	0.142012	0.225474	intron-variant	Rnf170	Mm_Celera	8:26137272	CTCCCAAGGGAAAGC[A/G]CAGTTTTGATACCAC	77733
rs37357309	snp	A/G	0.124444	0.216185	intron-variant, downstream-variant-500B	Rnf170	Mm_Celera	8:26130442	CTTTTTGTTTTATCC[A/G]TTGAACCTACAGATC	77733
rs37484903	snp	A/G	0.165289	0.235211	intron-variant	Rnf170	Mm_Celera	8:26134869	TGAACATCACCTAGT[A/G]CAATAAGTACTTCAG	77733
rs37496114	snp	A/G	0.124444	0.216185	intron-variant	Rnf170	Mm_Celera	8:26133634	GAGCTCCATGAAGGC[A/G]CAGGCACGAGGTAAT	77733
rs37512126	snp	A/G	0.142012	0.225474	intron-variant	Rnf170	Mm_Celera	8:26132817	CTCTAGTTAGAGGAA[A/G]AGATATTTGAGATTA	77733
rs37538320	snp	C/T	0.260355	0.249785	utr-variant-3-prime, nc-transcript-variant	Rnf170	Mm_Celera	8:26143117	TAAGAGTGGCATGCA[C/T]CATAGAAAACTGTGG	77733
rs37555134	snp	C/T	0.336735	0.234472	intron-variant	Rnf170	Mm_Celera	8:26137229	CCAGCACCTCAAGAC[C/T]TTGCCTTATTCTTCA	77733
rs37689001	snp	G/T	0.35503	0.226867	intron-variant	Rnf170	Mm_Celera	8:26138489	CTTATATTTTCTTAT[G/T]ACAAAAAGGACTGGT	77733
rs37780840	snp	C/T	0.336735	0.234472	upstream-variant-2KB, intron-variant	Rnf170, Hook3	Mm_Celera	8:26117805	ACAAAACAGTGATGG[C/T]TACCTTCCAGAGATC	77733
rs37804886	snp	A/T	0.35503	0.226867	intron-variant	Rnf170	Mm_Celera	8:26140292	CTTGGCTTATTTTAT[A/T]AGATTATTGATCAGT	77733
rs38024586	snp	C/T	0.408163	0.193609	intron-variant	Rnf170	Mm_Celera	8:26132089	TTGACCCTCCTTCTT[C/T]CTGAATCTAAACAAG	77733
rs38405530	snp	A/G	0.336735	0.234472	intron-variant	Rnf170	Mm_Celera	8:26137300	CACCTGCAATGCCAG[A/G]TAACAGGCTCTGGAA	77733
rs38408571	snp	A/G	0.142012	0.225474	intron-variant	Rnf170	Mm_Celera	8:26135253	ATATTTTTCCAATAC[A/G]TCAAATTTGTAACAA	77733
rs38835289	snp	C/T	0.32	0.24	upstream-variant-2KB, intron-variant	Rnf170, Hook3	Mm_Celera	8:26118108	ATATATGCCTGGACC[C/T]ACCTCCAACCAGCAT	77733
rs38840281	snp	C/T	0.260355	0.249785	intron-variant, downstream-variant-500B	Rnf170	Mm_Celera	8:26135984	CCCAGTGTTAGCAGT[C/T]TTAAATTTAAACTGA	77733
rs39959963	snp	A/G	0.124444	0.216185	upstream-variant-2KB, intron-variant	Rnf170, Hook3	Mm_Celera	8:26117989	ACAAAATTAACATGT[A/G]TCACAATAGCCACTG	77733
rs46317094	snp	C/T			intron-variant	Rnf170	GRCm38.p3	8:26140662	TCTAGTAACTAATTT[C/T]TAAATAAAATGCATA	77733
rs47784942	snp	C/T			intron-variant	Rnf170	Mm_Celera	8:26134455	ATCACAGTCTAGGAA[C/T]CTTCACATTGCCACT	77733
rs48348562	snp	C/T			intron-variant	Rnf170	Mm_Celera	8:26139914	AGAACACTTGTCTGC[C/T]AAGTGCCTAGGTTCA	77733
rs48441819	snp	C/T			intron-variant	Rnf170	Mm_Celera	8:26125121	GAGTTGTCACAGGGT[C/T]GCCTAGAGTGCAGAG	77733
rs49275079	snp	C/T			intron-variant, upstream-variant-2KB	Rnf170, Hook3	Mm_Celera	8:26121078	AAGCAAATAAATAAC[C/T]GTATCTGAAGCCTTC	77733
rs51316901	snp	C/T			intron-variant	Rnf170	Mm_Celera	8:26125073	ATTTGTCATTTAAAC[C/T]TAAAGTCAGCTGATG	77733
rs52564382	snp	A/T			intron-variant	Rnf170	Mm_Celera	8:26139685	tttatttatttattt[A/T]tatatgcttgagtgc	77733
rs211890865	snp	C/T			intron-variant	Rnf170	Mm_Celera	8:26131048	CACTAAGGTTTTTTT[C/T]CCCCCACATACCTAA	77733
rs211978730	snp	A/C			utr-variant-3-prime, nc-transcript-variant	Rnf170	Mm_Celera	8:26142034	CACACACACACACAC[A/C]CACCCCACAATCACA	77733
rs212015113	snp	C/T			intron-variant	Rnf170	Mm_Celera	8:26140343	TTAGGTTTAGAACCA[C/T]TTATCTGAAATACTT	77733
rs212130800	snp	C/T			intron-variant	Rnf170	Mm_Celera	8:26123026	GCATCTACATACTCT[C/T]AAAGAGATTCCTTTA	77733
rs212274929	snp	G/T			intron-variant	Rnf170	Mm_Celera	8:26132147	GCAGGCAAAATGAAC[G/T]TATTTGCCAACTCAG	77733
rs212326404	in-del	-/TGTT			intron-variant	Rnf170	Mm_Celera	8:26122098	GTGTGTGTGTGTGTG[-/TGTT]TTTTAAAGATTTATT	77733
rs212485088	snp	A/T			intron-variant	Rnf170	GRCm38.p3	8:26122119	AAGATTTATTTATTA[A/T]ATGTAAGCACACTGT	77733
rs212589247	snp	A/G			intron-variant	Rnf170	Mm_Celera	8:26133895	TCACCATTGCACAAT[A/G]TGAGGTTGAGCTATC	77733
rs212676552	in-del	-/TCTCTCTC			intron-variant	Rnf170	Mm_Celera	8:26127257	ACTTCCTTTTTTATT[-/TCTCTCTC]TCTCTCTCTCTCTCT	77733
rs213125123	snp	C/T			intron-variant	Rnf170	Mm_Celera	8:26126736	TGGATATGGTGTTAC[C/T]TCACGTTCTCCACAG	77733
rs213207629	snp	A/G			intron-variant	Rnf170	Mm_Celera	8:26137094	TCATTTAACCTGGAG[A/G]CAAGACAGTAGAAAG	77733

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