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
rs4230848	snp	A/G	0.48	0.0979796	utr-variant-3-prime, nc-transcript-variant	Gga1, LOC102632079	GRCm38.p3	15:78894585	GACAAGAGCAGCTAA[A/G]CCAGGAAAAAAGTCA	106039
rs4230849	snp	A/G	0.32	0.24	utr-variant-3-prime, nc-transcript-variant	Gga1, LOC102632079	GRCm38.p3	15:78894514	CCTACTTGACCACAG[A/G]AGGGTGGGCAGATGT	106039
rs4230850	snp	C/T	0.32	0.24	utr-variant-3-prime, nc-transcript-variant	Gga1, LOC102632079	GRCm38.p3	15:78894492	GGCAGATGTGAGGTG[C/T]TCCCGGGAGGCCCCA	106039
rs4230851	snp	C/G	0.32	0.24	utr-variant-3-prime, nc-transcript-variant	Gga1, LOC102632079	GRCm38.p3	15:78894431	GGGAGTTCCATGGCC[C/G]TCCAGGGGGCATGTC	106039
rs4230852	snp	C/T	0.32	0.24	utr-variant-3-prime, nc-transcript-variant	Gga1, LOC102632079	GRCm38.p3	15:78894335	GCCCCGGGGGCTGAG[C/T]GGAGAGCTCCTTCAG	106039
rs13461022	snp	G/T	0.48	0.0979796	utr-variant-3-prime, downstream-variant-500B	Gga1, LOC102632079	GRCm38.p3	15:78894168	AGGCCCAGCCATAAC[G/T]TGGAGGCCATGCTGG	106039
rs13461023	snp	C/T			utr-variant-3-prime, downstream-variant-500B	Gga1, LOC102632079	GRCm38.p3	15:78894041	GGAGCAGGGAGGGGC[C/T]GTATGCCCTGGAAGG	106039
rs31566767	snp	A/G	0.231111	0.249285	intron-variant	Gga1	Mm_Celera	15:78885052	AAGGAACTACTGTTT[A/G]CAAGTTATATATATT	106039
rs31566769	snp	C/T	0.459184	0.136902	intron-variant	Gga1	Mm_Celera	15:78885445	TGTGGAGGTGGCATC[C/T]TGTGTGGAGCCGGCT	106039
rs31566771	snp	A/G	0.142012	0.225474	intron-variant	Gga1	Mm_Celera	15:78886027	TGTGCGTGTGTGTAC[A/G]TATGATGTCCTATAG	106039
rs31566773	snp	G/T	0.32	0.24	intron-variant	Gga1	Mm_Celera	15:78886099	GCTCAGAGGCTGATA[G/T]TTAGAGGGAAGTAGC	106039
rs31567695	snp	A/G	0.408163	0.193609	intron-variant	Gga1	Mm_Celera	15:78887249	TGACCGCAGGAAAAG[A/G]AACGATCAAGGCCAC	106039
rs31567697	snp	A/G	0.244898	0.249948	intron-variant	Gga1	Mm_Celera	15:78887390	GAAATCTCCCAGCTC[A/G]CTAATGACAGCAGCA	106039
rs31567699	snp	A/T	0.231111	0.249285	intron-variant	Gga1	Mm_Celera	15:78887427	CTTTCCACGTTTTAA[A/T]AGTGTGTGCCCCACC	106039
rs31567701	snp	A/G	0.459184	0.136902	intron-variant	Gga1	Mm_Celera	15:78887626	ATGTGAGGCTGCCAA[A/G]CACAAGCCTACCTCC	106039
rs31567703	snp	C/T	0.124444	0.216185	synonymous-codon	Gga1	Mm_Celera	15:78888155	GCGGGTGAATGCCAT[C/T]GAGGAGGTCAACAAC	106039
rs31568525	snp	C/T	0.32	0.24	intron-variant	Gga1	GRCm38.p3	15:78888687	TCCTGTGCAGGCATC[C/T]TATCTGCCCAGGAGG	106039
rs31568527	snp	A/G	0.32	0.24	intron-variant	Gga1	GRCm38.p3	15:78888761	TCACAGCCCCAGTGT[A/G]TCACATCACCCCTTC	106039
rs31568529	snp	C/T	0.231111	0.249285	synonymous-codon	Gga1	GRCm38.p3	15:78889070	GCAGCTGGTCCGGGG[C/T]GAGGAGGTCAACGGT	106039
rs31568531	snp	C/T	0.32	0.24	synonymous-codon	Gga1	GRCm38.p3	15:78889088	GGAGGTCAACGGTGA[C/T]GCCACAGCCAGCTCC	106039
rs31568533	snp	A/G	0.32	0.24	intron-variant	Gga1	GRCm38.p3	15:78889456	TTTGGGTATGAGAGC[A/G]GCAGCCATATCTTAA	106039
rs31569205	snp	G/T	0.32	0.24	intron-variant	Gga1	GRCm38.p3	15:78889564	TAAGCAAAGCTGGTT[G/T]ATTGTGAACAAAAGA	106039
rs31569207	snp	A/G	0.231111	0.249285	synonymous-codon, upstream-variant-2KB	Gga1, Mir6955	GRCm38.p3	15:78889855	CCTGCTTGATGACGA[A/G]CTCATGTCTCTGGGT	106039
rs31569209	snp	C/T	0.244898	0.249948	intron-variant, upstream-variant-2KB	Gga1, Mir6955	GRCm38.p3	15:78889984	CGAGCAGCATGGCTT[C/T]CCTATTCTGGGTGAA	106039
rs31569211	snp	C/T	0.495868	0.0452663	intron-variant, upstream-variant-2KB	Gga1, Mir6955	GRCm38.p3	15:78891174	CCTGCTCTTAGCTGC[C/T]GAGGGCCCAAGGTGA	106039
rs31569213	snp	A/G	0.48	0.0979796	intron-variant, upstream-variant-2KB	Gga1, Mir6955	GRCm38.p3	15:78891185	CTGCCGAGGGCCCAA[A/G]GTGAAAGTTCCAACT	106039
rs31569975	snp	A/G	0.336735	0.234472	intron-variant, upstream-variant-2KB	Gga1, Mir6955	GRCm38.p3	15:78891249	ACGGAGAGGAAGTTA[A/G]TGTGGGCTGCAAGGT	106039
rs31569977	snp	C/T	0.489796	0.070696	intron-variant, upstream-variant-2KB	Gga1, Mir6955	GRCm38.p3	15:78891271	CTGCAAGGTGGCTGC[C/T]GGGATGATGCTTTCT	106039
rs31569979	snp	A/G	0.473373	0.11227	intron-variant, upstream-variant-2KB	Gga1, Mir6955	GRCm38.p3	15:78891588	GAGAGGTGACAGGCA[A/G]GTGGGTCCTGGGACA	106039
rs31569981	snp	C/T	0.244898	0.249948	intron-variant, upstream-variant-2KB	Gga1, Mir6955	GRCm38.p3	15:78891604	GTGGGTCCTGGGACA[C/T]GGCAGTACCATCCCA	106039
rs31569983	snp	A/G	0.32	0.24	intron-variant, upstream-variant-2KB	Gga1, Mir6955	GRCm38.p3	15:78891809	TCTATTATCCTCTCT[A/G]CTGTACCTCTCTCAG	106039
rs31570784	snp	C/T	0.231111	0.249285	synonymous-codon, downstream-variant-500B	Gga1, Mir6955	GRCm38.p3	15:78892022	AGCGGCCTGGACGAC[C/T]TGGACCTCTTGGGGA	106039
rs31570786	snp	G/T	0.231111	0.249285	intron-variant	Gga1	GRCm38.p3	15:78892428	CCACTACAAAATCAC[G/T]TGCTAATACACTGTC	106039
rs31570787	snp	C/G	0.32	0.24	intron-variant	Gga1	GRCm38.p3	15:78893036	AGAATGCATGACCCA[C/G]ACTTTGAACAGAGCC	106039
rs31570789	snp	C/T	0.244898	0.249948	intron-variant	Gga1	GRCm38.p3	15:78893493	TGGGAAGGGAGCTGC[C/T]TCTGCTGTGGTGGCT	106039
rs31570790	snp	C/T	0.444444	0.157135	intron-variant	Gga1	GRCm38.p3	15:78893679	CTGACGTGGCAGTGC[C/T]CCAGGGTGGCGCTAA	106039
rs31570792	snp	A/C	0.124444	0.216185	synonymous-codon, downstream-variant-500B	Gga1, LOC102632079	GRCm38.p3	15:78893751	GAAGGTTCGCCTCCG[A/C]TACAAGCTCATCTTC	106039
rs31571784	snp	A/C	0.124444	0.216185	utr-variant-3-prime, nc-transcript-variant	Gga1, LOC102632079	GRCm38.p3	15:78894384	GCTCTCAGGCTCCCA[A/C]GGGCCATGGAAACTT	106039
rs31571785	snp	C/T	0.32	0.24	downstream-variant-500B, nc-transcript-variant	Gga1, LOC102632079	GRCm38.p3	15:78894586	GACTTTTTTCCTGGA[C/T]TAGCTGCTCTTGTCA	106039
rs31571786	snp	G/T	0.489796	0.070696	downstream-variant-500B, nc-transcript-variant	Gga1, LOC102632079	GRCm38.p3	15:78894827	GGAGGTCTGGCTGCT[G/T]CAGAAGTCAAGGGGA	106039
rs31571787	snp	C/T	0.244898	0.249948	downstream-variant-500B, nc-transcript-variant	Gga1, LOC102632079	GRCm38.p3	15:78894890	GCAGCCGGTCTTGTG[C/T]TTCTCCCTGCCCGAC	106039
rs31571789	snp	C/T	0.32	0.24	downstream-variant-500B, nc-transcript-variant	Gga1, LOC102632079	GRCm38.p3	15:78894914	GCCCGACACACGGCT[C/T]TCTCCAAAGCCCTGC	106039
rs31571791	snp	C/T	0.124444	0.216185	downstream-variant-500B, nc-transcript-variant	Gga1, LOC102632079	GRCm38.p3	15:78894952	CTACTCTTCACCCGG[C/T]GTGGTAAAAGGCTGG	106039
rs45780045	snp	G/T			upstream-variant-2KB	Gga1	GRCm38.p3	15:78875339	ggcgggaagcagtgt[G/T]cattccacactctct	106039
rs45792305	snp	A/G			intron-variant	Gga1	GRCm38.p3	15:78878607	GGTTGATTGGTGGTT[A/G]GAAGGAGACAGTGAC	106039
rs45938022	snp	G/T			upstream-variant-2KB	Gga1	GRCm38.p3	15:78875718	GTAGCTGGAGATGTC[G/T]CTCAGTTGGTAGCGT	106039
rs45966445	snp	C/T			intron-variant	Gga1	GRCm38.p3	15:78893689	AGTGCCCCAGGGTGG[C/T]GCTAACCTCCCTTCC	106039
rs45987147	snp	C/T			intron-variant	Gga1	GRCm38.p3	15:78879627	CACCCACAAGGTTCC[C/T]GGGATAGATTGGTAC	106039
rs46001773	snp	A/T			upstream-variant-2KB	Gga1	GRCm38.p3	15:78876578	TTCCCCATCACCTTG[A/T]GAGTGTTACGTGCTT	106039
rs46005111	snp	A/G			upstream-variant-2KB	Gga1	GRCm38.p3	15:78876985	CTTCAGGACTGCCAG[A/G]GCAAGACAGTGAGCC	106039
rs46144458	snp	C/T			intron-variant	Gga1	GRCm38.p3	15:78879250	GTGGGGTCATGTCTC[C/T]TCCAGTTCTAAGATC	106039
rs46174362	snp	A/G			intron-variant	Gga1	GRCm38.p3	15:78892814	AACCCTGACCCCCTC[A/G]TTCCCAGGGAGGGCA	106039
rs46269678	snp	A/G			intron-variant	Gga1	Mm_Celera	15:78885783	GACCATTTCACAGAG[A/G]GGTCCCACACACAGT	106039
rs46325074	snp	C/T			intron-variant	Gga1	GRCm38.p3	15:78880884	GCCCACTGATCCCAC[C/T]GGAAGGTCAGTGCTC	106039
rs46431853	snp	A/T			intron-variant	Gga1	GRCm38.p3	15:78878920	GCTCAGCCTGCTCTC[A/T]TATAGAACCAAGACT	106039
rs46514386	snp	C/T			synonymous-codon, downstream-variant-500B	Gga1, Mir6955	GRCm38.p3	15:78892009	TCCACCAACGAGCAG[C/T]GGCCTGGACGACCTG	106039
rs46577148	snp	G/T			intron-variant	Gga1	GRCm38.p3	15:78880761	CAGCGTGAGAGATGG[G/T]AAAGTCAGCGTAGTG	106039
rs46632470	snp	A/G			intron-variant	Gga1	GRCm38.p3	15:78880967	ACCCCTCTTAACTGC[A/G]CCAGTTGCAGGACAG	106039
rs46779864	snp	A/G			intron-variant	Gga1	Mm_Celera	15:78886404	GGAAGGGAAGAATCA[A/G]TTTTCACAAGTGCCC	106039
rs46783089	snp	C/T			intron-variant	Gga1	Mm_Celera	15:78887707	ATGCCTTTAAAGGCC[C/T]GGACCCACACACTGG	106039
rs46945337	snp	A/G			intron-variant	Gga1	GRCm38.p3	15:78889144	GGCTCTGGGGGGCCC[A/G]GGTGCGGGGCGGCAT	106039
rs47156381	snp	G/T			intron-variant	Gga1	GRCm38.p3	15:78886672	GATGTTAATATGTTT[G/T]TTTTTTTGTTTTTTT	106039
rs47245797	snp	A/G			intron-variant	Gga1	GRCm38.p3	15:78882551	CACCACTGCCCGACC[A/G]TAGGACACATGTTAA	106039
rs47273124	snp	A/G			upstream-variant-2KB	Gga1	GRCm38.p3	15:78876066	GCGCCACCACTGCCC[A/G]GCCTGCAGTTGGGTT	106039
rs47371218	snp	C/G			intron-variant	Gga1	GRCm38.p3	15:78881355	TTACCGGGACATGAG[C/G]AGTCCTACACCTGGT	106039
rs47379383	snp	A/G			intron-variant	Gga1	GRCm38.p3	15:78880805	GGAGGCCGTCCCTGG[A/G]TGTAGTCTCTGAGGA	106039
rs47390346	snp	G/T			upstream-variant-2KB	Gga1	GRCm38.p3	15:78875325	GTGAGTGGAGAAAGG[G/T]CGGGAAGCAGTGTGC	106039
rs47400003	snp	C/T			upstream-variant-2KB	Gga1	GRCm38.p3	15:78876894	GCGTGGTGGCACACT[C/T]CTTTAATGTCTGCAC	106039
rs47449461	snp	A/G			intron-variant	Gga1	GRCm38.p3	15:78881264	GGCTTCAGGGGTGCC[A/G]CCCCCTTGAGGGGAG	106039
rs47739007	snp	C/G			intron-variant	Gga1	GRCm38.p3	15:78878508	GAAGCCAGCCTCGAA[C/G]GAAGTTGAACTGGAA	106039
rs47790171	snp	A/G			intron-variant	Gga1	Mm_Celera	15:78884995	GGATTAAAGGCGTGC[A/G]CCACCACCGCCCGGC	106039
rs47896452	snp	A/T			upstream-variant-2KB	Gga1	GRCm38.p3	15:78875961	ggttttgttctgtgt[A/T]gccctgggtcctgga	106039
rs47906703	snp	C/T			upstream-variant-2KB	Gga1	GRCm38.p3	15:78875417	CTTGATTTCTCCTCC[C/T]CTTGAATTGTGGGAA	106039
rs48084533	snp	C/G			intron-variant	Gga1	GRCm38.p3	15:78878407	CCCAGAGAAGCCTTC[C/G]GGTCTATCCTCAAGC	106039
rs48189477	snp	G/T			intron-variant	Gga1	GRCm38.p3	15:78879241	GGGAAAGGGGTGGGG[G/T]CATGTCTCTTCCAGT	106039
rs48231196	snp	C/T			intron-variant	Gga1	Mm_Celera	15:78886335	AGCAAGATGGCTCTA[C/T]AGGTATAGATATCCG	106039
rs48329896	snp	A/G			intron-variant	Gga1	Mm_Celera	15:78886755	GATCAGGCTGGCCTC[A/G]AACTCAGAAATCTGC	106039
rs48332840	snp	A/C			upstream-variant-2KB	Gga1	GRCm38.p3	15:78876659	TCTGATAAGTGCGGG[A/C]GTTATCATCACCTTG	106039
rs48370797	snp	G/T			intron-variant	Gga1	GRCm38.p3	15:78882654	AGACCACATAGGATC[G/T]GTAGACCCTGAACTT	106039
rs48371264	snp	C/T			intron-variant	Gga1	Mm_Celera	15:78886590	GGTGGCTGTCCTCTG[C/T]ATCCCCCAAACATAT	106039
rs48542079	snp	A/G			intron-variant	Gga1	GRCm38.p3	15:78893090	GGCTCCAGGGTGGGC[A/G]TCCTGCCTCTAAGAG	106039
rs48587971	snp	A/G			intron-variant	Gga1	GRCm38.p3	15:78884455	ATGCTTGCCTAGCAT[A/G]CACGAAGCTCTGCCT	106039
rs48771128	snp	C/T			intron-variant	Gga1	GRCm38.p3	15:78883975	CAGCTCCACCAGGCC[C/T]CTTGCAGGGCCTATG	106039
rs48802643	snp	A/G			upstream-variant-2KB	Gga1	GRCm38.p3	15:78875682	CAGCTTGGGCTATAA[A/G]GACTCTAGATGGAGG	106039
rs49068853	snp	A/T			downstream-variant-500B, nc-transcript-variant	Gga1, LOC102632079	GRCm38.p3	15:78894829	AGGTCTGGCTGCTGC[A/T]GAAGTCAAGGGGAAG	106039
rs49069268	snp	C/T			upstream-variant-2KB	Gga1	GRCm38.p3	15:78876589	CTTGAGAGTGTTACG[C/T]GCTTTGAGATACGAT	106039
rs49430977	snp	C/T			intron-variant	Gga1	GRCm38.p3	15:78882351	TGATGGCAGGGATTC[C/T]TTAACTCACACACAA	106039
rs49847499	snp	G/T			upstream-variant-2KB	Gga1	GRCm38.p3	15:78875215	TCGATGAGCTGCTGC[G/T]CGTGCCTCAGGAGGA	106039
rs49960345	snp	A/G			intron-variant	Gga1	GRCm38.p3	15:78881567	CCTGGGTGATAGAAC[A/G]CTCCGCACAGTGAGC	106039
rs50036506	snp	A/G			intron-variant	Gga1	GRCm38.p3	15:78882033	GGCATGTGCTTCACA[A/G]GGCCAGTAGAGGGCT	106039
rs50263917	snp	C/T			intron-variant	Gga1	GRCm38.p3	15:78880530	CCTGAGCAGAGCGGC[C/T]CTCAGCCTGGGCAGC	106039
rs50269545	snp	C/T			intron-variant	Gga1	Mm_Celera	15:78886742	AACTCACCCTGTAGA[C/T]CAGGCTGGCCTCGAA	106039
rs50683809	snp	A/C			upstream-variant-2KB	Gga1	GRCm38.p3	15:78875698	GACTCTAGATGGAGG[A/C]AGAAGTAGCTGGAGA	106039
rs51079585	snp	A/G			intron-variant	Gga1	GRCm38.p3	15:78880920	TGGGGGTGTCCAGCA[A/G]GAAGTGGAGGGAATC	106039
rs51164168	snp	A/G			intron-variant	Gga1	Mm_Celera	15:78886225	AACTCCAGAGGCTGA[A/G]GCAGGAGGATCCTGA	106039
rs51164886	snp	C/T			intron-variant	Gga1	Mm_Celera	15:78886734	TGTCCTGGAACTCAC[C/T]CTGTAGATCAGGCTG	106039
rs51241765	snp	A/G			upstream-variant-2KB	Gga1	GRCm38.p3	15:78875637	CTGCCTAACATGTTT[A/G]TATGAAATGCTAGGT	106039
rs51340145	snp	C/T			intron-variant	Gga1	Mm_Celera	15:78885965	GGCTGGCCTGGTGTA[C/T]AGGGGTAGAAGGGAT	106039
rs51349120	snp	C/T			intron-variant	Gga1	Mm_Celera	15:78886928	CAGCACTTGGGAGGC[C/T]GAGGCAGGAGGAATT	106039
rs51429961	snp	A/T			intron-variant	Gga1	Mm_Celera	15:78887024	TCTCAAGACAGAAAA[A/T]TTTCAAAAGGTGTTG	106039

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