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
rs729496	snp	C/G	0.499878	0.00781361	upstream-variant-2KB	LONRF3	GRCh38.p7	X:118974350	TTCTCTTGGGCTTCT[C/G]AGTCTCCAAACCCCA	79836
rs907798	snp	A/G	0.0333324	0.12472	intron-variant	LONRF3	GRCh38.p7	X:118983843	AGAAAGGAATAGTTA[A/G]CAAAATCAATGAAAT	79836
rs1031565	snp	C/T	0.132815	0.220834	intron-variant	LONRF3	GRCh38.p7	X:118978031	TACACACGGCTAGTG[C/T]CCGGCAGCCTGGTTT	79836
rs1398869	snp	A/G	0.113499	0.209446	intron-variant	LONRF3	GRCh38.p7	X:118977378	CCACATTCCCCTGGA[A/G]GTTCTTCCTTGCATC	79836
rs1455862	snp	A/G	0.435961	0.167089	intron-variant	LONRF3	GRCh38.p7	X:119001960	ATATTATTTGATGGT[A/G]CTAATGATGAAGATG	79836
rs1807937	snp	C/T	0.482857	0.0909818	intron-variant	LONRF3	GRCh38.p7	X:118996217	ctttcaacttttccc[C/T]gttcagtattatgAC	79836
rs1975779	snp	A/G/T	0	0	intron-variant	LONRF3	GRCh38.p7	X:118979282	Agcgcggtggctcac[A/G/T]cctgtaatcccagca	79836
rs2100524	snp	A/T	0.497754	0.0334346	intron-variant	LONRF3	GRCh38.p7	X:118993193	acctcttcaattctt[A/T]ttcaggtaaatcaag	79836
rs2100525	snp	A/G	0.48927	0.0724549	intron-variant	LONRF3	GRCh38.p7	X:118992810	tgggtctctcagtag[A/G]tagataccagtgcct	79836
rs2100526	snp	C/T	0.497754	0.0334346	intron-variant	LONRF3	GRCh38.p7	X:118992778	ttctggtggaggtgg[C/T]ggtgggtgcaatgga	79836
rs2100527	snp	A/T	0.49779	0.0331715	intron-variant	LONRF3	GRCh38.p7	X:118992775	tggtggaggtggtgg[A/T]gggtgcaatggactc	79836
rs2124399	snp	C/T	0.477825	0.102937	intron-variant	LONRF3	GRCh38.p7	X:119015403	ACTGGTGTCTTAGAA[C/T]CTCAGAATGCAAGAG	79836
rs2124400	snp	C/T	0.486987	0.0796057	intron-variant	LONRF3	GRCh38.p7	X:119015306	CTTCCCAAGGTCATA[C/T]TGCTAGTGAGGTAAG	79836
rs2124401	snp	A/G	0.478269	0.101948	intron-variant	LONRF3	GRCh38.p7	X:119015235	TTTCTTTTGTGACAG[A/G]GTTGGGGATGAGCAT	79836
rs2168377	snp	G/T	0.0369084	0.130736	intron-variant	LONRF3	GRCh38.p7	X:119015476	TGCCTTTGCATGGGG[G/T]GGGAAAGAAGCCACC	79836
rs2168378	snp	C/G	0.30475	0.243931	intron-variant	LONRF3	GRCh38.p7	X:119015168	ATAGGAAGAGATGGT[C/G]GTGAGGAAATATGTG	79836
rs2168379	snp	C/T	0.471939	0.115078	intron-variant	LONRF3	GRCh38.p7	X:119009080	CAATTAGGTAATACG[C/T]AGCAATCAGCAAAAC	79836
rs2278954	snp	C/T	0.473172	0.11267	synonymous-codon, nc-transcript-variant	LONRF3	GRCh38.p7	X:119014266	ATGAAACCACAATGA[C/T]GCTTGCTGATAGACA	79836
rs2290514	snp	A/C	0.486294	0.081639	intron-variant, downstream-variant-500B, nc-transcript-variant	LONRF3	GRCh38.p7	X:119013270	TGAGAAATCCTTTCA[A/C]AACTATCTTTGTGTA	79836
rs2316007	snp	G/T	0.0414859	0.13792	intron-variant	LONRF3	GRCh38.p7	X:119016695	TCACAACCTCACTTT[G/T]CAAAAATTCCAATTA	79836
rs2316008	snp	A/G	0.447004	0.153913	intron-variant	LONRF3	GRCh38.p7	X:119010208	GAGAGCCTCAATGAC[A/G]CCTCTGCCCCTCCCC	79836
rs2316009	snp	C/T	0.0348667	0.127349	intron-variant	LONRF3	GRCh38.p7	X:119010168	CACATTACCTGTGCA[C/T]GGCAGAGAAAGCGCT	79836
rs2316010	snp	G/T	0.0414859	0.13792	intron-variant	LONRF3	GRCh38.p7	X:118995805	ttattggtctgttca[G/T]ggtatctcatccttc	79836
rs3049095	in-del	-/GTCT	0.0235569	0.105941	intron-variant	LONRF3	GRCh38.p7	X:118977089	TGTTTAGTCTTTTCT[-/GTCT]TTTTTCTTCTGCAGC	79836
rs3747384	snp	C/G	0.32817	0.237465	intron-variant	LONRF3	GRCh38.p7	X:118990277	AGAGGTTTCCAGCAG[C/G]CCCAACAGAAAGAGA	79836
rs3813933	snp	A/G	0.496518	0.0415792	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	LONRF3	GRCh38.p7	X:118974822	GTCGCTGCTGACCTC[A/G]GCGGGCAAGCTCAGC	79836
rs3813935	snp	A/C	0.166434	0.23562	upstream-variant-2KB	LONRF3	GRCh38.p7	X:118974127	CCGTGAAGCCCCCCC[A/C]CACACACACAACCCA	79836
rs3827453	snp	C/G	0.455119	0.14292	intron-variant	LONRF3	GRCh38.p7	X:118990731	CAGGGAATGCAGTCT[C/G]TGGGAAGGGGACACA	79836
rs4581223	snp	A/C	0	0	intron-variant	LONRF3	GRCh38.p7	X:118997398	tttcaacaaatggtg[A/C]tgggataattggcta	79836
rs4825394	snp	A/T	0.498408	0.028167	intron-variant	LONRF3	GRCh38.p7	X:118994056	aatcctggaaacaca[A/T]caaaacagaacctct	79836
rs4825623	snp	C/T	0.305742	0.243707	intron-variant	LONRF3	GRCh38.p7	X:118988331	TGAAAAGAAGAAAAA[C/T]AGCAACCTTGGCTTT	79836
rs4825625	snp	C/T	0.389954	0.207154	intron-variant	LONRF3	GRCh38.p7	X:119009855	GCTTACTGCAACCTC[C/T]GCCTTCCGGGTTCAA	79836
rs5903535	in-del	-/C			upstream-variant-2KB	LONRF3	GRCh38.p7	X:118974492	CGAAGCCCAAAGAAG[-/C]CAAGAGCAACACTGT	79836
rs5909579	snp	A/G	0.300422	0.244862	intron-variant	LONRF3	GRCh38.p7	X:118980632	GTTTTTTTTCCCCAA[A/G]GAACACATTTAGTGT	79836
rs5909580	snp	C/T	0.323794	0.238861	intron-variant	LONRF3	GRCh38.p7	X:118984714	GATGATGCAAGCGAG[C/T]GTATGCCCGTGATGA	79836
rs5909581	snp	C/T	0.0142023	0.083063	intron-variant	LONRF3	GRCh38.p7	X:118987829	CTGCACTATGCCTTA[C/T]ACATAAGTAAGCTTC	79836
rs5909583	snp	A/G	0.499113	0.0210409	intron-variant	LONRF3	GRCh38.p7	X:119002451	ttattgcatataggt[A/G]aagtttgttcacttt	79836
rs5910465	snp	A/G	0.465403	0.126891	intron-variant	LONRF3	GRCh38.p7	X:118978896	ctaataatgtaaggt[A/G]cttagaacagtgtct	79836
rs5910466	snp	C/T	0.438029	0.164757	intron-variant	LONRF3	GRCh38.p7	X:118978897	TAATAATGTAAGGTA[C/T]TTAGAACAGTGTCTG	79836
rs5910467	snp	A/G	0.377438	0.21508	intron-variant	LONRF3	GRCh38.p7	X:118980222	CCTTATCTGAATCTT[A/G]TAAGACCAGAGGTGT	79836
rs5910468	snp	A/T	0.389207	0.207657	intron-variant	LONRF3	GRCh38.p7	X:118980356	AAAATTCACACTCAG[A/T]GGGACAAATATTTTT	79836
rs5910469	snp	C/T	0.462705	0.131365	intron-variant	LONRF3	GRCh38.p7	X:118983627	TCATGGACTTTGTTG[C/T]TTATTGTTCTACAGT	79836
rs5910470	snp	C/T	0.463996	0.129251	intron-variant	LONRF3	GRCh38.p7	X:118984722	AAGCGAGTGTATGCC[C/T]GTGATGAGTGTTACA	79836
rs5910471	snp	A/G	0.240609	0.249824	intron-variant	LONRF3	GRCh38.p7	X:118986529	TTCTCTCCTGACTTT[A/G]CCTCTCTGTCTCTTT	79836
rs5910473	snp	G/T	0.462849	0.13113	intron-variant	LONRF3	GRCh38.p7	X:118989802	CTCTGGCATTTACTA[G/T]CTGTGTGACCTCAGA	79836
rs5910474	snp	A/C	0.495428	0.0475954	intron-variant	LONRF3	GRCh38.p7	X:118991255	CGCCCCCGCCACCCA[A/C]CTGCCTTATTCCAAC	79836
rs5910479	snp	C/T	0.017851	0.0927731	intron-variant	LONRF3	GRCh38.p7	X:119000566	TGTGGTTACCTTAGC[C/T]ATTGGGGGCCACCTC	79836
rs5910480	snp	A/C	0.435581	0.16751	intron-variant	LONRF3	GRCh38.p7	X:119003500	gtattgaaaatcttt[A/C]ccccatctgctttga	79836
rs5910481	snp	C/T	0.497847	0.0327373	intron-variant, nc-transcript-variant	LONRF3	GRCh38.p7	X:119012847	atggtagCAGTTACA[C/T]GAATACATTACGAAT	79836
rs5956093	snp	A/G	0.438029	0.164757	intron-variant	LONRF3	GRCh38.p7	X:118981374	CCTGTAGTCCCAGCT[A/G]CTCAGGAGGCTGAGG	79836
rs5956094	snp	C/T	0.325989	0.238171	intron-variant	LONRF3	GRCh38.p7	X:118981416	CTTGAACCTAGGAGG[C/T]GGAGGTTGTAGTGAG	79836
rs5956095	snp	C/T	0.489115	0.0729673	intron-variant	LONRF3	GRCh38.p7	X:118988557	GTTTTCTCCCAGCTA[C/T]ATGCTCCCCTTTTTC	79836
rs5956096	snp	C/T	0.0965482	0.197364	intron-variant	LONRF3	GRCh38.p7	X:118996660	aggtgcggtggctca[C/T]gcctgtaatcccagc	79836
rs5956098	snp	A/C	0.30475	0.243931	intron-variant, downstream-variant-500B, nc-transcript-variant	LONRF3	GRCh38.p7	X:119013655	ATAATCCATCATCCC[A/C]TAAGGCAGAAAGATG	79836
rs5957086	snp	G/T	0.389207	0.207657	intron-variant	LONRF3	GRCh38.p7	X:118981365	TGACGCATGCCTGTA[G/T]TCCCAGCTACTCAGG	79836
rs5957087	snp	A/T	0.46256	0.131599	intron-variant	LONRF3	GRCh38.p7	X:118987419	AGTAGCTGGGACTAT[A/T]GGCACGTGCCACCAT	79836
rs5957088	snp	C/T	0.482561	0.0917346	intron-variant	LONRF3	GRCh38.p7	X:118987424	CTGGGACTATAGGCA[C/T]GTGCCACCATGCCTG	79836
rs5957090	snp	A/G	0.483919	0.0882151	intron-variant	LONRF3	GRCh38.p7	X:118997865	atggccaacaaacat[A/G]aagaaatgctcagca	79836
rs5957091	snp	A/G	0.0733812	0.176934	intron-variant	LONRF3	GRCh38.p7	X:118998940	gctgggattacaggc[A/G]tgagccactatgcct	79836
rs5957093	snp	C/T	0.426333	0.177219	intron-variant	LONRF3	GRCh38.p7	X:119006883	gtgagccaccacgcc[C/T]ggcctaatttttgta	79836
rs5957094	snp	A/C	0.453518	0.145191	intron-variant	LONRF3	GRCh38.p7	X:119016504	AGAAGCCCGCCACCG[A/C]GCCCGGCTAATTTTT	79836
rs5957095	snp	A/G	0.30475	0.243931	intron-variant	LONRF3	GRCh38.p7	X:119016704	TTTTTGCAAAGTGAG[A/G]TTGTGATTCTTTGGG	79836
rs6603457	snp	C/T	0.482561	0.0917346	intron-variant	LONRF3	GRCh38.p7	X:118986681	TTCCTGGGCCACACT[C/T]CAGACCTGGGGGAGA	79836
rs6603465	snp	A/G	0.496821	0.0397406	intron-variant, downstream-variant-500B, nc-transcript-variant	LONRF3	GRCh38.p7	X:119013502	AAGATTGCAAGGAAT[A/G]GATCTGGGGTGGGTC	79836
rs6645535	snp	G/T	0.0806904	0.183941	intron-variant	LONRF3	GRCh38.p7	X:119000971	ACAAGGATGTAACTG[G/T]TGGGAAAAGATAGCT	79836
rs6645536	snp	A/G	0.0738704	0.177421	intron-variant	LONRF3	GRCh38.p7	X:119009863	CAACCTCCGCCTTCC[A/G]GGTTCAAGCGATTCT	79836
rs6646305	snp	C/T	0.0845627	0.187431	intron-variant, utr-variant-5-prime	LONRF3	GRCh38.p7	X:118976595	CCCGCTTTTCAGTGC[C/T]GCCTGGGAGGGTTGG	79836
rs6646306	snp	C/T	0.0903376	0.192374	intron-variant	LONRF3	GRCh38.p7	X:118979069	GCAGTGGCGCAATCT[C/T]GGCTCACTGCAACCT	79836
rs6646308	snp	C/T	0.0797195	0.183042	intron-variant	LONRF3	GRCh38.p7	X:118980125	CAAGCTATAAAGCTT[C/T]CTGGATGTAGTGCTC	79836
rs6646309	snp	A/G	0	0	intron-variant	LONRF3	GRCh38.p7	X:118980584	CATTTTTTTTTCTGA[A/G]AAGGTTTTCTTGAGT	79836
rs6646314	snp	A/G	0.0738704	0.177421	intron-variant	LONRF3	GRCh38.p7	X:119010197	TGAGAGGTGAAGGGG[A/G]GGGGCAGAGGCGTCA	79836
rs6646315	snp	C/T	0.0669955	0.170321	intron-variant	LONRF3	GRCh38.p7	X:119016095	AGTGAGATTTGGTGA[C/T]GATCAGAGGAACCAA	79836
rs7053662	snp	G/T	0.089378	0.191574	intron-variant	LONRF3	GRCh38.p7	X:119005060	AGCTGGCATGTTGCT[G/T]CTTCTACTCAGTCTG	79836
rs7054507	snp	G/T	0.0845627	0.187431	intron-variant	LONRF3	GRCh38.p7	X:118983928	TGCTTTGAATTGGTT[G/T]GAGTATGTGAAAAAG	79836
rs7054825	snp	A/C	0.00787002	0.062234	intron-variant	LONRF3	GRCh38.p7	X:118993129	tctaacacccccccc[A/C]aaaaaccacactagt	79836
rs7063603	snp	A/G	0.0430067	0.140192	intron-variant	LONRF3	GRCh38.p7	X:118979211	gttttcaccgtgtta[A/G]ccaggatggtctcga	79836
rs7064296	snp	A/G	0.0826288	0.185706	intron-variant	LONRF3	GRCh38.p7	X:118988164	CTGAAATGCAGGTGC[A/G]CCCAACTTTTCTTAA	79836
rs7066489	snp	A/C	0.00528398	0.051128	intron-variant	LONRF3	GRCh38.p7	X:119016501	tacagaagcccgcca[A/C]cgcgcccggctaatt	79836
rs7067172	snp	C/G	0.0440191	0.141675	intron-variant	LONRF3	GRCh38.p7	X:118984069	ttgagaatttcttct[C/G]cattatacactgtgc	79836
rs7879672	snp	A/G	0.018891	0.0953342	utr-variant-3-prime, nc-transcript-variant	LONRF3	GRCh38.p7	X:119017904	GCTTCTTGACATGCT[A/G]CATAACTACATAAAC	79836
rs7882263	snp	A/G	0.0105399	0.0718252	intron-variant	LONRF3	GRCh38.p7	X:118993562	aataataatcggtgt[A/G]cctgtggaagaagaa	79836
rs7883690	snp	C/T	0.496693	0.0405276	intron-variant	LONRF3	GRCh38.p7	X:119016053	AGAATGCAAATGAAG[C/T]TAGAGGCACAAAGAA	79836
rs9792799	snp	A/C	0.000529661	0.016265	intron-variant	LONRF3	GRCh38.p7	X:118981634	CCTTGGTAAACACTG[A/C]TGGGAGAAGCAACAA	79836
rs10127384	snp	A/G	0.0748481	0.178387	intron-variant	LONRF3	GRCh38.p7	X:119006562	catgccaccacgctc[A/G]gctaatttttgtttt	79836
rs10465423	snp	A/G	0.462849	0.13113	intron-variant	LONRF3	GRCh38.p7	X:118989127	GCATTTCCCCTTTTT[A/G]CACCTGCCCAAGGAG	79836
rs10587850	in-del	-/TTGTT			intron-variant	LONRF3	GRCh38.p7	X:119006601	TTGTTTTGTTTTGTT[-/TTGTT]GAGACGGAGTCTCGC	79836
rs10640705	in-del	-/T/TC/TT/TTCC/TTTCT/TTTT			intron-variant	LONRF3	GRCh38.p7	X:119016366	TTTTTTTTTTTTTTT[-/T/TC/TT/TTCC/TTTCT/TTTT]GAGACGGAGTCTTGC	79836
rs10669908	in-del	-/AAA			intron-variant	LONRF3	GRCh38.p7	X:118981499	AAAAAAAAAAAAAAA[-/AAA]GAGTATATGGATTGC	79836
rs11377517	in-del	-/A/AA			utr-variant-3-prime, nc-transcript-variant	LONRF3	GRCh38.p7	X:119019161	AAAAAAAAAAAAAAA[-/A/AA]GGGAACCAGATAATC	79836
rs11406051	in-del	-/T	0.498408	0.028167	intron-variant	LONRF3	GRCh38.p7	X:118991393	TGTCACCACCACAGA[-/T]CTATTCTTGGGAAGC	79836
rs12156701	snp	A/C			synonymous-codon, nc-transcript-variant, utr-variant-3-prime, intron-variant	LONRF3	GRCh38.p7	X:119013054	GTTTGCAGAATATGG[A/C]TGCATCCTAGAGATC	79836
rs12391696	snp	C/T	0.390203	0.206986	intron-variant	LONRF3	GRCh38.p7	X:118983100	AGATGGGAGTGTTAA[C/T]TGATTGCCCAGAAAC	79836
rs12556024	snp	C/T	0.00158814	0.0281345	intron-variant	LONRF3	GRCh38.p7	X:118996399	tgctgatgatatgat[C/T]gtttaccttgaaaac	79836
rs12558411	snp	C/T	0.436528	0.166455	intron-variant	LONRF3	GRCh38.p7	X:119003856	tccaatagaggtctc[C/T]tacaactgttgttag	79836
rs12687273	snp	A/G	0.000529661	0.016265	intron-variant	LONRF3	GRCh38.p7	X:119007983	TTTAGTATCAGCAGA[A/G]GAGTCACCTACTTTT	79836
rs12832094	snp	A/T			intron-variant	LONRF3	GRCh38.p7	X:119014599	GCAGGTTTTGAGAAC[A/T]AAGTAAGATAAGAGA	79836
rs12838954	snp	A/G	0.0348667	0.127349	intron-variant	LONRF3	GRCh38.p7	X:119004233	TATTAGTTTTAATTA[A/G]TTTGTTAAACAAATT	79836
rs12843423	snp	C/G/T	0.0772873	0.180749	intron-variant	LONRF3	GRCh38.p7	X:118990967	agttcaagcgattca[C/G/T]gtgcctcagcctctt	79836
rs12844427	snp	A/G			intron-variant	LONRF3	GRCh38.p7	X:118978857	agcagctactaaaga[A/G]ggctgttgtgaggat	79836
rs12844457	snp	A/G			intron-variant	LONRF3	GRCh38.p7	X:118978901	aatgtaaggtactta[A/G]aacagtgtctggcat	79836

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