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
rs717454	snp	A/G	0.48953	0.0716355	intron-variant	REV1	GRCh38.p7	2:99406310	GGTTGGTGGTCATCA[A/G]TGTGGTTCTTTTTTA	51455
rs737094	snp	C/T	0.258843	0.249844	intron-variant	REV1	GRCh38.p7	2:99472616	ACCCCACCTGAAGAT[C/T]CTGTCCACTGCAGCT	51455
rs769105	snp	C/T	0.480144	0.097642	intron-variant	REV1	GRCh38.p7	2:99461504	CAGGTCTCCATGCCT[C/T]GCTTTCCCTTGATAG	51455
rs896248	snp	A/G	0.480302	0.0972668	intron-variant	REV1	GRCh38.p7	2:99462013	GAAATTTTACTTCCT[A/G]AACTGTGAGAATTCA	51455
rs896249	snp	A/G	0.480144	0.097642	intron-variant	REV1	GRCh38.p7	2:99472750	AATTTACAAGAACCA[A/G]GTATTGCCTTTATGA	51455
rs959929	snp	C/G	0.486725	0.0803809	intron-variant	REV1	GRCh38.p7	2:99461864	AATGTGCAAATGCTT[C/G]TTTGCCTGTTGCACA	51455
rs1000409	snp	A/G	0.486725	0.0803809	intron-variant	REV1	GRCh38.p7	2:99441727	AATAATTACTTTCAT[A/G]AAAATCCATGAAAAA	51455
rs1011633	snp	A/G	0.480223	0.0974544	intron-variant	REV1	GRCh38.p7	2:99478337	gtggtttggaacaca[A/G]gaaagCAGGAAAATT	51455
rs1046340	snp	A/G	0	0	synonymous-codon, nc-transcript-variant	REV1	GRCh38.p7	2:99403060	AGCAGTGaaagaaaa[A/G]aaaagaaacaagaag	51455
rs1053544	snp	C/T	0.47852	0.101384	intron-variant	REV1	GRCh38.p7	2:99405808	TTTTATTTCTTCATC[C/T]GTTTAACCAAGAAAG	51455
rs1451243	snp	A/T	0.484701	0.0861117	intron-variant	REV1	GRCh38.p7	2:99423818	TGAAATAAAAGAGAA[A/T]AACCAGGTTAAAAAA	51455
rs1451245	snp	A/G	0.287606	0.247155	intron-variant, upstream-variant-2KB	REV1	GRCh38.p7	2:99441027	AAGTAAAATCTAAAA[A/G]GTAATTTCTTCCTAA	51455
rs1451246	snp	A/C	0.488572	0.0888507	intron-variant	REV1	GRCh38.p7	2:99447821	CATCTCCTGGGTTCA[A/C]GCGATTCTCCTGCCT	51455
rs1451248	snp	C/T	0.00318978	0.0398085	upstream-variant-2KB	REV1	GRCh38.p7	2:99491777	TCTTCGGTTTGAATA[C/T]GAGAGTGGAAAAGAA	51455
rs1839666	snp	A/G	0.480223	0.0974544	intron-variant	REV1	GRCh38.p7	2:99486480	cttgcagtgagccaa[A/G]atggtgccactgcac	51455
rs1839667	snp	C/T	0.480302	0.0972668	intron-variant	REV1	GRCh38.p7	2:99447802	TCAGCTCACTGGAGC[C/T]TCCCATCTCCTGGGT	51455
rs1901283	snp	C/T	0.487049	0.0794222			GRCh38.p7	2:99444099	TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC	51455
rs1973011	snp	C/G	0.480223	0.0974544	intron-variant	REV1	GRCh38.p7	2:99470456	caaaatttattcaaa[C/G]acctgtgctaacatt	51455
rs2053916	snp	C/T	0	0	intron-variant	REV1	GRCh38.p7	2:99445786	AGGATTCCCTTGCCT[C/T]TTCAAAGTCAGGGCC	51455
rs2053917	snp	C/T	0.480144	0.097642	intron-variant	REV1	GRCh38.p7	2:99454422	ggatgtggtggcatg[C/T]gcctgtaactccagc	51455
rs2122748	snp	A/T	0.480144	0.097642	intron-variant	REV1	GRCh38.p7	2:99448907	TAGGCTATAGTATTA[A/T]CAACATGAGCTTAAA	51455
rs2242037	snp	C/T	0.48435	0.0870631	intron-variant	REV1	GRCh38.p7	2:99412644	CTTAATTTCAAGCAT[C/T]GAGGGTCTAATGGTT	51455
rs2290257	snp	C/G	0.477684	0.103247	downstream-variant-500B, utr-variant-3-prime	REV1, EIF5B	GRCh38.p7	2:99400250	ATCTGTTTTAGTAGA[C/G]ATTTTTATACATTAA	51455
rs2290258	snp	A/C	0.198324	0.244601	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	REV1, EIF5B	GRCh38.p7	2:99400611	AGAAGCAAAAAGACA[A/C]CACCACCTCTGATCT	51455
rs2290259	snp	C/T	0.00478085	0.0486577	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	REV1, EIF5B	GRCh38.p7	2:99400628	ACCACCTCTGATCTA[C/T]GGGACATAATGTTCC	51455
rs2290260	snp	C/T	0.000708116	0.0188031	synonymous-codon, nc-transcript-variant	REV1	GRCh38.p7	2:99404492	TCCTGCGTCACTGTT[C/T]GATTCTTGAGGTTCT	51455
rs2290261	snp	A/G	0.488151	0.0760519	intron-variant	REV1	GRCh38.p7	2:99404721	AGTTAAAGCATGCTC[A/G]GAGATGAGGTGTTTG	51455
rs2305354	snp	A/G	0.487304	0.0786571	synonymous-codon, nc-transcript-variant	REV1	GRCh38.p7	2:99403033	CCTTTTTGGTGAACC[A/G]ATGGTTTTTTTCTTC	51455
rs2309585	snp	A/G	0.484771	0.0859212	intron-variant, upstream-variant-2KB	REV1	GRCh38.p7	2:99440155	CATAACATTTGTCAT[A/G]GGTTCTGCATTTATA	51455
rs2309604	snp	C/T	0.480223	0.0974544	intron-variant	REV1	GRCh38.p7	2:99473636	TGTAAAAAAAACACA[C/T]AAAGTGGCAAAAATG	51455
rs3070575	in-del	-/T			intron-variant	REV1	GRCh38.p7	2:99442252	ttttttttttttttt[-/T]gagatggagttttgc	51455
rs3071397	in-del	-/GT	0.476833	0.105105	intron-variant	REV1	GRCh38.p7	2:99471139	CCAAAGGCAAATTGT[-/GT]TTCAACCTTGCCTAG	51455
rs3071414	in-del	-/ATAG	0.487305	0.0786545	intron-variant	REV1	GRCh38.p7	2:99461021	CGTTAATGAAAACAG[-/ATAG]GCATTGCTTCTTACA	51455
rs3087382	snp	C/T	0.0114282	0.0747228	intron-variant	REV1	GRCh38.p7	2:99462480	GTTGAGTACTTTTTA[C/T]TTAACCCTATTTTGG	51455
rs3087383	snp	C/G/T	0.0025732	0.0357808	intron-variant	REV1	GRCh38.p7	2:99410903	AGGTATATAGGAAAG[C/G/T]GGAATGGTAGTTTCT	51455
rs3087384	snp	C/T	1.65236e-05	0.00287429	intron-variant	REV1	GRCh38.p7	2:99462462	AACCCTATTTTGGCA[C/T]GTATTTTTATTAGGA	51455
rs3087385	snp	C/G	0.0387226	0.133648	intron-variant	REV1	GRCh38.p7	2:99410689	ACATTGCCAGGTAAG[C/G]TCACCTCAGAAATGA	51455
rs3087386	snp	C/T	0.488589	0.0746691	missense, utr-variant-5-prime, nc-transcript-variant	REV1	GRCh38.p7	2:99439044	GGCTTTCTCCAGCCT[C/T]TTCCCAGGAGGAGGA	51455
rs3087387	snp	C/T	0.0693013	0.172766	intron-variant	REV1	GRCh38.p7	2:99401405	AAAAGGAATAATTAG[C/T]CTTAAGGACCTTTCC	51455
rs3087388	snp	A/C	0.00129669	0.0254296	missense, nc-transcript-variant	REV1	GRCh38.p7	2:99403095	TTAGTGCCAAAGAAT[A/C]CTTTACTTCATCTAA	51455
rs3087389	snp	G/T	0.0459516	0.144445	intron-variant	REV1	GRCh38.p7	2:99403884	ACAAAGTCTGTTTTG[G/T]GAAAAAGAGAAACCA	51455
rs3087390	snp	A/G	0.00066589	0.0182346	intron-variant	REV1	GRCh38.p7	2:99442304	GGTGTAAGTTTGTCT[A/G]GTTGGGGATTACTGC	51455
rs3087391	snp	A/G	0.0111728	0.0739025	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	REV1	GRCh38.p7	2:99438800	CAAGGCAGCACCTTC[A/G]GTGCCATCCAAACCT	51455
rs3087392	snp	A/C	0.0109286	0.0731087	missense, nc-transcript-variant	REV1	GRCh38.p7	2:99403001	TTCAGAGTCCTTTGA[A/C]TAACAAGCTGCTTAA	51455
rs3087393	snp	C/G	0.0109286	0.0731087	missense, nc-transcript-variant	REV1	GRCh38.p7	2:99403051	agaaaagaaaagaaa[C/G]aagaagaaaaaaaCC	51455
rs3087394	snp	A/G	9.91867e-05	0.00704155	missense, nc-transcript-variant	REV1	GRCh38.p7	2:99412937	GGAGTTGGACATTCA[A/G]TGGAATCTAAGTTGG	51455
rs3087395	snp	A/G	0.116488	0.211364	intron-variant	REV1	GRCh38.p7	2:99421370	TTAGCATTGCTTACA[A/G]TTGTGTGACACACGA	51455
rs3087396	snp	G/T	0.00291422	0.0380607	missense, nc-transcript-variant	REV1	GRCh38.p7	2:99405959	TACATACTCCTGTCA[G/T]TGTGCAGTCGAGACT	51455
rs3087397	in-del	-/C	0.48071	0.0962957	intron-variant	REV1	GRCh38.p7	2:99403150	GTCATCCAGACTATC[-/C]ATACTATCATTTTGT	51455
rs3087398	snp	G/T	0.00345422	0.0414147	missense, nc-transcript-variant	REV1	GRCh38.p7	2:99412924	CAATGGAATCTAAGT[G/T]GGCATCTTTGGGAAT	51455
rs3087399	snp	A/G	0.238426	0.249732	missense, utr-variant-5-prime, nc-transcript-variant	REV1	GRCh38.p7	2:99438696	TGACTGAGTTTGTCA[A/G]TACCCTACAAAGACA	51455
rs3087400	snp	C/T	0.00187697	0.0305772	missense, nc-transcript-variant	REV1	GRCh38.p7	2:99402968	GTCCTGCAAAAACTC[C/T]GCCAGGGGCCTGTGG	51455
rs3087401	snp	A/G	0.0620919	0.164896	missense, nc-transcript-variant	REV1	GRCh38.p7	2:99404482	GAATCGAACAGTGAC[A/G]CAGGAATAAATTTAA	51455
rs3087402	snp	C/T	0.0109286	0.0731087	intron-variant	REV1	GRCh38.p7	2:99435944	CTGTCTTTTTCCTTC[C/T]AGGAGATATGTCAGT	51455
rs3087403	snp	A/G	0.391914	0.205816	missense, utr-variant-5-prime, nc-transcript-variant	REV1	GRCh38.p7	2:99442408	ACCAAGCAGTCCAGT[A/G]TGCAGAAAGGTCTCA	51455
rs3209289	snp	A/G	0	0	missense, nc-transcript-variant	REV1	GRCh38.p7	2:99403065	AAGGCAGCAGTGaaa[A/G]aaaagaaaagaaaca	51455
rs3749087	snp	C/T	0.47852	0.101384	intron-variant	REV1	GRCh38.p7	2:99410478	GTTGGTTTGACGGCA[C/T]TGCTGACCTTGGCAG	51455
rs3792134	snp	A/G	0.487049	0.0794222	intron-variant	REV1	GRCh38.p7	2:99464127	ATTTATTGTGAGGTG[A/G]ATGTTATCTAATGAA	51455
rs3792135	snp	A/G	0.287606	0.247155	intron-variant	REV1	GRCh38.p7	2:99445701	TTTTGTAAATCTCAC[A/G]CTTGTACATAGTGTA	51455
rs3792136	snp	C/T	0.2768	0.248559	intron-variant	REV1	GRCh38.p7	2:99445311	TTCAGTTTATCTTTT[C/T]TTTCTAAACTCCCAA	51455
rs3792137	snp	G/T	0.480144	0.097642	intron-variant	REV1	GRCh38.p7	2:99445286	TCCCAAACCATATAC[G/T]TTTGTCATGTGCTTA	51455
rs3792138	snp	G/T	0.122554	0.216665	intron-variant	REV1	GRCh38.p7	2:99444537	CCATGGACTGACTTA[G/T]GTAAGCCTAAGAATT	51455
rs3792141	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	REV1	GRCh38.p7	2:99440772	TTCTGACGTACATCA[C/T]TTTTGTTGTTTTCTG	51455
rs3792142	snp	G/T	0.478768	0.100824	intron-variant, upstream-variant-2KB	REV1	GRCh38.p7	2:99440746	TTCTGGGGTTTTTTT[G/T]GGGGGTATATTCAGT	51455
rs3792143	snp	A/G	0.280785	0.248097	intron-variant, upstream-variant-2KB	REV1	GRCh38.p7	2:99440558	CATGATCATCTGTGA[A/G]CATGGCATCTACTCA	51455
rs3792144	snp	A/G	0.479824	0.098392	intron-variant, upstream-variant-2KB	REV1	GRCh38.p7	2:99440274	ACATTCCTAAGTAGA[A/G]TGAATTACTGCTTTG	51455
rs3792146	snp	A/G	0.485187	0.0847778	intron-variant	REV1	GRCh38.p7	2:99435060	ATTTCTTGGTCCTCA[A/G]AATAATGCATTAAGT	51455
rs3792147	snp	A/G	0.00755907	0.0610114	intron-variant	REV1	GRCh38.p7	2:99435012	TGCTATTGCTTTACA[A/G]ATTTATAGTAATCTT	51455
rs3792148	snp	C/T	0.195837	0.244062	intron-variant	REV1	GRCh38.p7	2:99434815	TGTTAACTCTAGAAA[C/T]ACAAAAAAAAATTTA	51455
rs3792149	snp	G/T	0.490673	0.0676508	intron-variant	REV1	GRCh38.p7	2:99430481	TGAAACCTCTTCATG[G/T]TTTGTGACCTACTAA	51455
rs3792150	snp	C/T	0.330249	0.23677	intron-variant	REV1	GRCh38.p7	2:99425387	TCTGTCATTTTCCTT[C/T]CTCTTAGGTATTTCT	51455
rs3792151	snp	G/T	0.293037	0.246268	intron-variant	REV1	GRCh38.p7	2:99425185	GTTTGTATATACGTT[G/T]CTTAAAACAAGGCAC	51455
rs3792152	snp	C/T	0.484491	0.0866827	intron-variant	REV1	GRCh38.p7	2:99415089	TGGAGGTACACCACA[C/T]GCCCTGCCTCCCTCC	51455
rs3792153	snp	C/T	0.0130921	0.0798413	utr-variant-3-prime, nc-transcript-variant	REV1	GRCh38.p7	2:99401082	AAGTGCCAAATTTGT[C/T]AGTATTGCATGTAAA	51455
rs3828316	snp	A/C	0.484632	0.086302	intron-variant	REV1	GRCh38.p7	2:99408357	CCATTACGGTTTTTA[A/C]CTTAAAGTTCTAGTG	51455
rs3838580	in-del	-/T	0.48498	0.0853497	intron-variant	REV1	GRCh38.p7	2:99434854	TTTAGTTTCTGTTGC[-/T]GTAAAATTGAGAGAT	51455
rs3838582	in-del	-/AA	0.282105	0.24793	intron-variant	REV1	GRCh38.p7	2:99414649	AAAAGAAATAACAAA[-/AA]GAGCAAATTGAAGAA	51455
rs3838583	in-del	-/ATTA	0.141934	0.225437	utr-variant-3-prime, nc-transcript-variant	REV1	GRCh38.p7	2:99401052	TAAATAATTGTGTTA[-/ATTA]TTTTACTGTAGCATA	51455
rs4143760	snp	A/C	0.480223	0.0974544	intron-variant	REV1	GRCh38.p7	2:99485300	CATCAATTCTTTCTT[A/C]TCTTATTTCTGTATC	51455
rs4341989	snp	C/T	0.34526	0.23114	intron-variant	REV1	GRCh38.p7	2:99430321	GGACTGTACAGCTCT[C/T]GGTAGTGGGGAAAAG	51455
rs4476396	snp	A/G	0.480144	0.097642	intron-variant	REV1	GRCh38.p7	2:99462981	TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	51455
rs4535093	snp	A/G	0.484209	0.0874434	intron-variant	REV1	GRCh38.p7	2:99419696	AAGAGTCCTCAAAAC[A/G]CAGAGACAGGCAGTG	51455
rs4851205	snp	A/C	0.48435	0.0870631	intron-variant	REV1	GRCh38.p7	2:99415610	CCACTGAGCACTTGC[A/C]ATGTGGCCAGGGCAG	51455
rs4851206	snp	C/T	0.480144	0.097642	intron-variant	REV1	GRCh38.p7	2:99451607	AGAAGTTGTTTAACT[C/T]CTTTAGGCTTTCTCC	51455
rs4851207	snp	G/T	0.281577	0.247998	intron-variant	REV1	GRCh38.p7	2:99489313	CTGTGGCTGGAGTGC[G/T]GGTGGGAGCGGCGGC	51455
rs4851208	snp	A/T	0.480144	0.097642	intron-variant	REV1	GRCh38.p7	2:99489455	GTTTGCGGCGCGGTC[A/T]GACCGGGCCGGCGGG	51455
rs4851209	snp	A/G	0.480144	0.097642	intron-variant	REV1	GRCh38.p7	2:99489506	AAGGGCCGCTGCGCC[A/G]GGGGTCGGCGCGGGG	51455
rs5832873	in-del	-/ATCT			intron-variant	REV1	GRCh38.p7	2:99461023	TAAGAAGCAATGCCT[-/ATCT]GTTTTCATTAACGTT	51455
rs5832874	in-del	-/A	0.5	0	intron-variant	REV1	GRCh38.p7	2:99471430	GTTAAAAAAAAACTT[-/A]AAAGTGTACAAAAGA	51455
rs5832875	in-del	-/C	0.000798403	0.0199641	intron-variant	REV1	GRCh38.p7	2:99477081	AGGGTGGTCTTGGGA[-/C]CCCCAACTCCACGAT	51455
rs6542879	snp	A/G	0.484841	0.0857308	intron-variant	REV1	GRCh38.p7	2:99431138	TTCCTGGTTTGACCA[A/G]TAATCATCAGCATCT	51455
rs6542880	snp	A/C	0.485118	0.0849685	intron-variant	REV1	GRCh38.p7	2:99437404	CCATAGTCCTGCAGC[A/C]TAAGAGTGGCAGAGT	51455
rs6542881	snp	A/C	0.479583	0.0989539	intron-variant	REV1	GRCh38.p7	2:99473409	AGAAAAAAGAAAAAA[A/C]TTCAGACACCTAGGT	51455
rs6542882	snp	C/T	0.485049	0.0851591	intron-variant, upstream-variant-2KB, utr-variant-5-prime	REV1	GRCh38.p7	2:99481151	CAAATAGATTATCAA[C/T]GCCTCCACCCTACCC	51455
rs6707685	snp	C/T	0.0733688	0.176922	intron-variant	REV1	GRCh38.p7	2:99476211	GGTAATCCTTTCTTT[C/T]CCCCCCCTTCACATG	51455
rs6711073	snp	A/G	0.47852	0.101384	intron-variant	REV1	GRCh38.p7	2:99404279	TGTCTACATCCTGCA[A/G]ATGCAGGAGATGGAG	51455
rs6713792	snp	C/G	0.490782	0.0672626	intron-variant	REV1	GRCh38.p7	2:99475163	gccatgagagtacaa[C/G]gaacaaaggagacag	51455
rs6714244	snp	A/G	0.48692	0.0798058	intron-variant	REV1	GRCh38.p7	2:99488850	GATACACAGAATTAC[A/G]GACTGTTACATAAAG	51455
rs6714650	snp	C/G	0.330714	0.236612	intron-variant	REV1	GRCh38.p7	2:99417332	tagttctagtagaga[C/G]agggtttcaccatgt	51455
rs6717515	snp	C/T	0.482234	0.0925596	intron-variant	REV1	GRCh38.p7	2:99428813	GCTAACACGGTGAAA[C/T]CCTGCCTCTACTAAA	51455

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