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
rs13475028	snp	C/T	0.375	0.216506	upstream-variant-2KB, missense	Usp19, Lamb2	GRCm38.p3	9:108489547	GCTCAGGGTGCCATC[C/T]GGGGAGCAGTGGTTG	71472
rs13475029	snp	C/T			upstream-variant-2KB, synonymous-codon	Usp19, Lamb2	Mm_Celera	9:108489255	CGAGCAGATCCAGCG[C/T]CTAGCCAGTGAGATT	71472
rs30166363	snp	G/T	0.5	0	intron-variant	Usp19	GRCm38.p3	9:108493980	TCTGTTTTTTTTTTT[G/T]TTTTGTGTGTGTGTG	71472
rs33640744	snp	C/T	0.375	0.216506	intron-variant	Usp19	Mm_Celera	9:108500600	GTTCTGATGTGTATT[C/T]GAGATATTCCCTATC	71472
rs45841050	snp	A/G	0.197531	0.244432	intron-variant	Usp19	GRCm38.p3	9:108491542	TCACTTTGGATGGAG[A/G]GAGCCCGAATCCACA	71472
rs45859985	snp	G/T	0.197531	0.244432	intron-variant	Usp19	GRCm38.p3	9:108493941	AGAGAGGGTACCACT[G/T]GCCGGACCAGAGCTA	71472
rs46040097	snp	C/T	0.18	0.24	intron-variant	Usp19	GRCm38.p3	9:108496025	TGAGTGTCCTGTGAG[C/T]GGATAGTTAAGATTT	71472
rs46156673	snp	A/G	0.32	0.24	synonymous-codon	Usp19	GRCm38.p3	9:108496379	CCTGTTTCAGGGCCA[A/G]TACAAGTCAAAGCTG	71472
rs46338515	snp	A/G	0.35503	0.226867	intron-variant	Usp19	GRCm38.p3	9:108500984	GATTGAAGGCTGTCT[A/G]CAGGAGGTCAAGACT	71472
rs47400315	snp	C/T	0.197531	0.244432	intron-variant	Usp19	GRCm38.p3	9:108492098	TCTCTACTTGTCTGG[C/T]GGTGACTAAGCAGCC	71472
rs47459327	snp	C/T	0.18	0.24	intron-variant	Usp19	GRCm38.p3	9:108493487	CCCTCTCTCCTGGTA[C/T]GTTCCAGTTGCGTGT	71472
rs48307923	snp	C/T	0.124444	0.216185	intron-variant, downstream-variant-500B	Usp19	Mm_Celera	9:108501719	GTCTCTCTGTCTAAA[C/T]GCCGCTGCTGTCTGC	71472
rs48760352	snp	A/G	0.124444	0.216185	intron-variant	Usp19	Mm_Celera	9:108499751	TCCTGTTCGGTGAGC[A/G]ATGAGTGAGGCCTGC	71472
rs48923636	snp	C/T	0.231111	0.249285	intron-variant	Usp19	GRCm38.p3	9:108497828	CAGGACTAAGCCCTC[C/T]GTGGTGCCGTGAAGC	71472
rs49493566	snp	A/C	0.197531	0.244432	synonymous-codon	Usp19	GRCm38.p3	9:108493188	GATTGTTAAGCTGCG[A/C]GTGGGAACAGGTCCC	71472
rs49981711	snp	C/G	0.231111	0.249285	utr-variant-3-prime, intron-variant, downstream-variant-500B	Usp19	GRCm38.p3	9:108502173	TGCCTTCAGTGCTGC[C/G]TGTTTGGTTCTCAGT	71472
rs50320341	snp	C/T			synonymous-codon	Usp19	Mm_Celera	9:108495911	GGCCCTATGGAAGGG[C/T]ACTCACCAAGCCTTT	71472
rs50460722	snp	C/T	0.165289	0.235211	upstream-variant-2KB, intron-variant	Usp19, Lamb2	Mm_Celera	9:108489138	GTCATGCAGGAGAGA[C/T]TGTTAAGCCCTTGCC	71472
rs50614059	snp	C/T	0.244898	0.249948	synonymous-codon	Usp19	GRCm38.p3	9:108498828	CCTTCTGAGCTCCAG[C/T]TGGTGACCCCTGTGG	71472
rs50922789	snp	G/T	0.244898	0.249948	intron-variant	Usp19	GRCm38.p3	9:108500681	TGTCCCTACTGAAAC[G/T]TCAGGCTCTTCTGTG	71472
rs51201795	snp	C/T	0.197531	0.244432	upstream-variant-2KB, intron-variant	Usp19, Lamb2	GRCm38.p3	9:108488942	GTACTTGAGTCTCGG[C/T]GTCTGCAATGGACAT	71472
rs212027787	snp	C/G			intron-variant, downstream-variant-500B	Usp19, Lamb2	GRCm38.p3	9:108490998	GGGCCGTGCCAGCCC[C/G]GACATCTCGAGCCTC	71472
rs212567353	snp	C/T			intron-variant	Usp19	GRCm38.p3	9:108492261	TCCAGCGTTGTGGGT[C/T]TCTGTAGATACCCAG	71472
rs212659025	snp	C/G			intron-variant	Usp19	Mm_Celera	9:108494284	AGATTGGGTTGCAGG[C/G]TTGGTGGGTGGGCAT	71472
rs213512879	snp	C/G			intron-variant	Usp19	GRCm38.p3	9:108500633	AGATGGCTGCTGCCT[C/G]GATTGGCTGTCACAC	71472
rs213634771	snp	G/T			intron-variant	Usp19	Mm_Celera	9:108499079	GGTGAGCACTGATGA[G/T]TGTGCTTTGTCTTAG	71472
rs213702387	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108491066	ATGCTACCCCTGTGG[C/T]CGGCCTCTCTGTTTT	71472
rs213828957	snp	A/G			upstream-variant-2KB, intron-variant	Usp19, Lamb2	GRCm38.p3	9:108489613	TGACTTCCTTAGGAC[A/G]AGGTGATGGGCATGT	71472
rs214645188	in-del	-/GGCTTTTCCAGAGTGCCTAC			intron-variant	Usp19	Mm_Celera	9:108492739	AGGAGAGGTAGGAGG[-/GGCTTTTCCAGAGTGCCTAC]GGCTTCCCTTATCAC	71472
rs214645914	snp	A/G			missense	Usp19	GRCm38.p3	9:108494157	CCGGTTATGGTCCAG[A/G]ACAGAGACCCTGAGC	71472
rs214786243	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108493335	TCCAGGTTACTTTTG[C/T]CACTCTTTTTACAGA	71472
rs214976468	snp	C/T			intron-variant	Usp19	GRCm38.p3	9:108497619	CTGCACTTATGTATT[C/T]TTTTCTTCTCTGGAT	71472
rs215799465	snp	G/T			synonymous-codon	Usp19	Mm_Celera	9:108499195	CCGTGAGCAGCGGCT[G/T]GAGGACAAAGGTGCC	71472
rs216085205	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108492222	CCACAACTGCCTTGA[C/T]CTAGCACTTCCTCAG	71472
rs216232291	snp	A/T			intron-variant	Usp19	Mm_Celera	9:108491492	GCTAGTACTAGGTCT[A/T]CGTTCCATCTCCACC	71472
rs216313224	snp	G/T			intron-variant	Usp19	Mm_Celera	9:108501085	TGCTTGATCTGGAAC[G/T]TGGGGGCTTACACCC	71472
rs217058650	in-del	-/G			intron-variant	Usp19	Mm_Celera	9:108491607	AGAGCTGATGATGAA[-/G]GAAGGAACCTGGAGA	71472
rs217601266	snp	A/G			synonymous-codon	Usp19	GRCm38.p3	9:108494231	TGATCCTACAGCCTT[A/G]GTGGAGGGTAACATG	71472
rs218577956	snp	A/G			intron-variant	Usp19	Mm_Celera	9:108495320	CCCGATTGCTCTTCC[A/G]AAGGTCTGGAGTTCA	71472
rs218717825	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108496600	GACTGAAGTCAGAGG[C/T]GTTTGTGTGCACAGG	71472
rs218973861	snp	A/G			intron-variant	Usp19	GRCm38.p3	9:108497690	TCCTTATGGAGGGTC[A/G]GTGAGGTTGATGCCT	71472
rs218992266	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108499035	ACTGCACTGAAGTGT[C/T]GGGAAGGCTGTTCCC	71472
rs219239034	snp	A/T			upstream-variant-2KB, synonymous-codon	Usp19, Lamb2	Mm_Celera	9:108489273	AGCCAGTGAGATTGC[A/T]GAACGCGTCCGAAGC	71472
rs219321484	snp	C/T			intron-variant	Usp19	GRCm38.p3	9:108497772	ATATTCCTCTTTTAG[C/T]CCACATATCATGTCC	71472
rs219435214	in-del	-/TTT			intron-variant	Usp19	Mm_Celera	9:108491687	GGAGTCCACTCCTCA[-/TTT]TTTTTTTTTTTTTCG	71472
rs219497611	snp	G/T			intron-variant, utr-variant-3-prime	Usp19	Mm_Celera	9:108501582	GGCAGAGTATCCTAG[G/T]GTGTGTGTCCATCCA	71472
rs219771531	snp	A/G			intron-variant	Usp19	Mm_Celera	9:108491670	TCACCGTGTCTTAAA[A/G]CTGGAGTCCACTCCT	71472
rs219788361	snp	A/G			utr-variant-3-prime, intron-variant, downstream-variant-500B	Usp19	Mm_Celera	9:108502099	GAGGGTGGGAACCTC[A/G]CAAGTTGTGACCTCT	71472
rs219827560	snp	A/G			intron-variant	Usp19	GRCm38.p3	9:108492345	GTAGCCTCACAGTGC[A/G]CATGGCTGCCTCAGC	71472
rs219904437	snp	C/G			intron-variant	Usp19	Mm_Celera	9:108499573	TTGCTGCTTCTGACT[C/G]CTCCTCTGTCGCTCA	71472
rs220488470	snp	A/G			upstream-variant-2KB, intron-variant	Usp19, Lamb2	GRCm38.p3	9:108490020	CCACTGAATTAGTAT[A/G]CCGACCCTGCCTCTT	71472
rs220584907	in-del	-/T			downstream-variant-500B	Usp19	Mm_Celera	9:108502618	CAGCCCAGCTCACTC[-/T]TAACTTCAGTCATAC	71472
rs220877115	snp	A/G			intron-variant	Usp19	Mm_Celera	9:108496748	CGATCTCTCCTGGTG[A/G]CTTCTGTTCCTCAGT	71472
rs220897932	snp	C/T			intron-variant	Usp19	GRCm38.p3	9:108494607	TTTGTCCTTCCTCTT[C/T]CTCTGCTCTGCCTCT	71472
rs220904313	snp	G/T			intron-variant	Usp19	Mm_Celera	9:108492800	GTATTGGGGTGGGGG[G/T]GGGGGTCCTGTCTCT	71472
rs220933935	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108491576	AGGTGGGAAACAGAT[C/T]AGGCCTCCGTGGCTC	71472
rs221014964	snp	C/T			missense	Usp19	GRCm38.p3	9:108493777	AGGGCTGTTCACCTC[C/T]GCAGAGGGCCAGAAG	71472
rs221135509	snp	A/G			intron-variant	Usp19	Mm_Celera	9:108493503	GTTCCAGTTGCGTGT[A/G]TGGGAGTTGGGGATA	71472
rs222054656	in-del	-/GTGTGTGTGTG			intron-variant	Usp19	GRCm38.p3	9:108493980	TCTGTTTTTTTTTTT[-/GTGTGTGTGTG]TGTGTGTGTGTGTGT	71472
rs222124457	snp	A/G			upstream-variant-2KB, intron-variant	Usp19, Lamb2	Mm_Celera	9:108489968	AGTGGGTTGGGCGAA[A/G]CCCTCTGGATGGGGT	71472
rs223316563	snp	C/G			downstream-variant-500B	Usp19	GRCm38.p3	9:108502644	CATACCCTTGCCTAT[C/G]GAGTAAATGGTGCTG	71472
rs224068850	in-del	-/T			intron-variant	Usp19	Mm_Celera	9:108497246	TTGTTCTTTTAAACA[-/T]TTTTTATGAGTGTTG	71472
rs224444504	snp	G/T			intron-variant	Usp19	Mm_Celera	9:108497861	AGCTGGAGAAAGGTC[G/T]CACCACATGCCATAT	71472
rs224538581	snp	A/G			intron-variant	Usp19	Mm_Celera	9:108493953	ACTGGCCGGACCAGA[A/G]CTAATCTTGCCTCTG	71472
rs224614046	snp	A/G			synonymous-codon	Usp19	Mm_Celera	9:108495131	CCTGACAGGCCAGGA[A/G]GAAGCCAGGGCTGTG	71472
rs225431972	snp	C/T			intron-variant	Usp19	GRCm38.p3	9:108497502	TTTTTTTCTTTTTTT[C/T]TGAGACAGAGTTTCT	71472
rs225551206	snp	A/G			intron-variant	Usp19	Mm_Celera	9:108492425	CCTTGTAGGCAGGGA[A/G]CAGATCACTTGGCCT	71472
rs225607168	snp	C/T			downstream-variant-500B	Usp19	Mm_Celera	9:108502350	CAACATGTTATGGCT[C/T]CCTCCCCGCCCTCCT	71472
rs225758728	snp	C/T			synonymous-codon	Usp19	Mm_Celera	9:108493426	GGCTCGCAAGGGTGG[C/T]CTTCTACAGCTAGTA	71472
rs225855718	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108491845	CACCCGCCTCCACTC[C/T]TAATCTTTAAGGCTG	71472
rs225897307	snp	A/T			upstream-variant-2KB, downstream-variant-500B	Usp19, Lamb2	GRCm38.p3	9:108490574	GGCGGAGGACCTTTA[A/T]ACACGCCATCAGCTG	71472
rs225953914	snp	C/T			downstream-variant-500B	Usp19	Mm_Celera	9:108502800	GTAGACTAGGCTAGC[C/T]TTGAACTCAGAGATC	71472
rs226112041	snp	C/G			synonymous-codon	Usp19	Mm_Celera	9:108498770	CACGTTGCTTTCAAC[C/G]AGCTCTCTGGAGGCT	71472
rs226623763	snp	A/G			synonymous-codon	Usp19	Mm_Celera	9:108494839	ACCAGAGCAGTGTAC[A/G]TTCTGTTTCACGGCC	71472
rs226806119	in-del	-/CCCTCCT			intron-variant	Usp19	Mm_Celera	9:108495968	GCTCACCCCCCCCCC[-/CCCTCCT]CACACACACACACCT	71472
rs227023380	snp	A/C			intron-variant	Usp19	GRCm38.p3	9:108498087	TGGGGGCAGTCACTG[A/C]TGCCTGCCCTTGCTG	71472
rs227083340	snp	G/T			intron-variant	Usp19	Mm_Celera	9:108495295	TGAGATGGCTTAGTG[G/T]GTAAGAGCACCCGAT	71472
rs227146963	snp	C/T			synonymous-codon	Usp19	Mm_Celera	9:108496213	GACTGTGGACTCGGA[C/T]GGGCGGCCCGATGAG	71472
rs227205785	snp	A/C			missense	Usp19	GRCm38.p3	9:108494178	GACCCTGAGCCTGAG[A/C]AAGAAGACCAAGTCA	71472
rs227277962	snp	A/G			intron-variant	Usp19	GRCm38.p3	9:108492891	GGCTTTCCACCTGAG[A/G]GACGTGGCTAAGATT	71472
rs227321552	snp	C/T			synonymous-codon	Usp19	Mm_Celera	9:108499418	TGAAGATCCAGGCTC[C/T]GCTGGTGAGGCTGCC	71472
rs227510732	snp	C/T			intron-variant	Usp19	GRCm38.p3	9:108499043	GAAGTGTTGGGAAGG[C/T]TGTTCCCACCAGAGT	71472
rs227819425	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108500436	TATATAAACACGATG[C/T]CACCAGTGTGCACAA	71472
rs228129513	in-del	-/A			intron-variant	Usp19	Mm_Celera	9:108491405	TATTTTTATCACCCC[-/A]CTCTCCCCTAAGGGA	71472
rs228425247	snp	C/G			upstream-variant-2KB, intron-variant	Usp19, Lamb2	Mm_Celera	9:108489099	CAGTCTGAGACCCCA[C/G]AATACCAAGATTGTG	71472
rs228756747	snp	G/T			intron-variant	Usp19	Mm_Celera	9:108492041	CCCTTCTGCTGCTCT[G/T]ACTATTCCTTGGTCT	71472
rs229152634	snp	C/G			intron-variant, downstream-variant-500B	Usp19, Lamb2	GRCm38.p3	9:108491006	CCAGCCCCGACATCT[C/G]GAGCCTCGCGGCGTG	71472
rs229196533	in-del	-/T			downstream-variant-500B	Usp19	Mm_Celera	9:108502717	CAAGTAGTCTTTTTG[-/T]TTTTTTTGTTTTTAT	71472
rs230072691	in-del	-/AAAAA			intron-variant	Usp19	Mm_Celera	9:108495444	TATAATAAATAAATT[-/AAAAA]AAAAAAAAAAAAAAA	71472
rs230961843	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108493292	ACCCCGAGAACAGGG[C/T]TACCTTTGAGTGCTC	71472
rs231368936	snp	A/G			intron-variant	Usp19	Mm_Celera	9:108494294	GCAGGGTTGGTGGGT[A/G]GGCATGGAGTAGTAC	71472
rs231464160	snp	A/C/T			intron-variant	Usp19	Mm_Celera	9:108495968	TGCTCACCCCCCCCC[A/C/T]CACACACACACACCT	71472
rs231491494	snp	C/T			intron-variant	Usp19	GRCm38.p3	9:108497786	GTCCACATATCATGT[C/T]CTGCCCCATCTCAGT	71472
rs232079372	snp	C/T			intron-variant	Usp19	Mm_Celera	9:108500296	GGGAGGCCTAACAGG[C/T]TAGTTGGGGGACAGA	71472
rs232084244	snp	A/G			synonymous-codon	Usp19	Mm_Celera	9:108499144	TGTGAATACCCACAC[A/G]CCCCAGTTCTTCATC	71472
rs232567478	snp	A/C			intron-variant	Usp19	GRCm38.p3	9:108492360	GCATGGCTGCCTCAG[A/C]TGGTGAGAATCCTGC	71472
rs232848670	snp	C/T			missense	Usp19	Mm_Celera	9:108498957	CCTATCGAAGGTTGT[C/T]CCTTGCTTGCTGGTG	71472
rs232996141	snp	A/T			upstream-variant-2KB, downstream-variant-500B, utr-variant-5-prime	Usp19, Lamb2	GRCm38.p3	9:108490664	AAGCTGCCCTTCACC[A/T]AGAGCTCCCACTCTT	71472
rs233027103	snp	C/T			upstream-variant-2KB, intron-variant	Usp19, Lamb2	Mm_Celera	9:108489763	TTTGTTAAACCTGGG[C/T]CTTTCTGTGGCAGGT	71472
rs233117720	snp	A/C/G			intron-variant	Usp19	GRCm38.p3	9:108491173	GGCAGCATCCTAGCC[A/C/G]GGGCGTTGGTCTGCG	71472

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