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
rs947932	snp	C/T	0.284733	0.247575	intron-variant	RNF121	GRCh38.p7	11:71945659	TGAGTCGTATTCTTC[C/T]TTGTATTTCAGAGAA	55298
rs1055452	snp	C/T	0.215446	0.2476	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996419	AAAGACTCAAAGGGG[C/T]GCTTGGGCCACTCAG	55298
rs1541306	snp	C/T	0.383053	0.211653	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71996967	TGTCCCAAAACAAAT[C/T]TTCAATGAATTCTGA	55298
rs1892920	snp	C/T	0.211819	0.247067			GRCh38.p7	11:71991385	tttgtaattctggca[C/T]atagctatgtgtcta	55298
rs1892921	snp	C/T	0.284733	0.247575			GRCh38.p7	11:71991092	agatagtttttcaac[C/T]gttgtccccactccc	55298
rs1939240	snp	A/C/T	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	IL18BP, RNF121	GRCh38.p7	11:71997733	CCTAGGGATGTCAGC[A/C/T]GGGGAACAGCTGGGA	55298
rs1939241	snp	C/T	0.215747	0.247642	intron-variant	RNF121	GRCh38.p7	11:71994083	ggaggccaaggaggg[C/T]ggatcacgaggtcag	55298
rs2032352	snp	A/G	0.137867	0.223442	intron-variant	RNF121	GRCh38.p7	11:71932912	CCCCTTTTCAGGAGG[A/G]ATGATTAGCCTGTTG	55298
rs2155141	snp	C/G	0.321769	0.239477	intron-variant	RNF121	GRCh38.p7	11:71931530	CGGATTTCACCTGCT[C/G]TTTCACAAGCTAAGG	55298
rs2155142	snp	C/T	0.184521	0.241273	intron-variant	RNF121	GRCh38.p7	11:71931478	GACATTAGTAGAAAC[C/T]TGAATACCAACTAAG	55298
rs2187496	snp	C/G	0.390464	0.206809	intron-variant	RNF121	GRCh38.p7	11:71940915	gctggaccactcact[C/G]ttccttacctcactg	55298
rs2276383	snp	A/G	0.077417	0.180873	intron-variant	RNF121	GRCh38.p7	11:71990486	AAGGCCCAAAGGCTA[A/G]AGCAAGTGCGGGCAA	55298
rs2276384	snp	C/T	0.211212	0.246973	intron-variant	RNF121	GRCh38.p7	11:71990477	AGGCTAGAGCAAGTG[C/T]GGGCAAACTATGACC	55298
rs2276385	snp	C/G	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71990456	AACTATGACCAAATC[C/G]AGTCTGCTGTCTATT	55298
rs2363736	snp	A/T	0.382666	0.211895	intron-variant	RNF121	GRCh38.p7	11:71945921	agttcaagaccagct[A/T]gggcaacatagagaa	55298
rs2363737	snp	A/G	0.212122	0.247114	intron-variant	RNF121	GRCh38.p7	11:71946117	ctctgccttaaaaaa[A/G]aaaagaaaagaaaag	55298
rs2885880	snp	A/G	0.382279	0.212137	intron-variant	RNF121	GRCh38.p7	11:71944801	GAAGGAAAAGATAGT[A/G]GATATATTTCTTACC	55298
rs3216157	in-del	-/A	1.76426e-05	0.00297001	intron-variant	RNF121	GRCh38.p7	11:71957317	CATATCACTCAATTA[-/A]GCTGGGTTAACCTGC	55298
rs3750914	snp	A/C	0.0930568	0.194599	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927995	CTGTAGCCCCAGCTC[A/C]CACGCCTCTGGGCGT	55298
rs3814722	snp	A/C	0.00597247	0.0543191	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997482	TATTCCCTAGAAACC[A/C]AATGCCGAAGGCCCA	55298
rs3829215	snp	A/G	0.184203	0.241186	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996443	CAGTCCGACACAGCC[A/G]GAGGGGTCCTGAGTG	55298
rs3841467	in-del	-/AC	0.272511	0.248984	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997204	CACACACACACACAC[-/AC]GCATACGCACTCTTA	55298
rs3886589	snp	G/T	0.284733	0.247575	intron-variant	RNF121	GRCh38.p7	11:71958441	TAGGTCTAATGGACT[G/T]AAGCTATAAGAAGAT	55298
rs3887002	snp	C/T	0.0402882	0.136092	intron-variant	RNF121	GRCh38.p7	11:71970597	GGCCCAGGAGTTTAA[C/T]GCTTCAGTAAACTAT	55298
rs3898386	snp	C/T	0.0337553	0.125452	intron-variant	RNF121	GRCh38.p7	11:71975360	ATTTCTCACACCTTC[C/T]TCAAATACTAGTTGT	55298
rs3915628	snp	C/T	0.0111196	0.0737302	intron-variant	RNF121	GRCh38.p7	11:71971567	AGATTAATATTtatc[C/T]agagaaactcctaca	55298
rs4121395	snp	C/T	0.284733	0.247575	intron-variant	RNF121	GRCh38.p7	11:71958196	GCATATTAAAAAGAT[C/T]TTTAACTGGATCATG	55298
rs4121396	snp	A/C	0	0	intron-variant	RNF121	GRCh38.p7	11:71958394	TGGGAAAGAAGAGTC[A/C]ATATGTCCTTTGTTG	55298
rs4399349	snp	C/T	0.213333	0.247296	intron-variant	RNF121	GRCh38.p7	11:71944327	AACAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAG	55298
rs4479013	snp	C/G	0.284733	0.247575	intron-variant	RNF121	GRCh38.p7	11:71962686	AACTTAAACTCATAT[C/G]TTTAGAAAATAAGAA	55298
rs4491255	snp	G/T	0.407158	0.194426	intron-variant	RNF121	GRCh38.p7	11:71973575	gcagatcacctgagg[G/T]tgggagttcaagacc	55298
rs4944232	snp	C/T	0.283947	0.247685	intron-variant	RNF121	GRCh38.p7	11:71931212	TGAAGGACTTGAGAG[C/T]GTCTAGTAGTATAAT	55298
rs4944242	snp	G/T	0.284995	0.247539	intron-variant	RNF121	GRCh38.p7	11:71956095	CAGTAGTAGAATGAA[G/T]TTCTACCTGTGTTAC	55298
rs4944243	snp	C/T	0.215747	0.247642	intron-variant	RNF121	GRCh38.p7	11:71963308	ggtcatagagattac[C/T]cttatgttttctttg	55298
rs4945353	snp	C/T	0.283684	0.24772	intron-variant	RNF121	GRCh38.p7	11:71930993	ATGCACCACCACGCC[C/T]GGCTGATTTTTTGTA	55298
rs4945378	snp	A/G	0.211819	0.247067	intron-variant	RNF121	GRCh38.p7	11:71957820	CATCATATATCTTAT[A/G]ATGATTGCTCATCAG	55298
rs4945382	snp	A/T	0.216649	0.247765	intron-variant	RNF121	GRCh38.p7	11:71962886	cactccgtttttttt[A/T]aaattttatttatta	55298
rs4945391	snp	A/T	0.211516	0.24702	intron-variant	RNF121	GRCh38.p7	11:71981438	TGTTGTTGTTTTTTT[A/T]AAAAATATTCTTTGA	55298
rs4945392	snp	C/T	0.215446	0.2476	intron-variant	RNF121	GRCh38.p7	11:71983599	GTAATTTAATATCTG[C/T]ACTCAACAGAAAAAG	55298
rs5743655	snp	C/T	0.00478085	0.0486577	upstream-variant-2KB, downstream-variant-500B	IL18BP, RNF121	GRCh38.p7	11:71997858	CTGAGGACAGTGTCC[C/T]GCCACCACCTGCCTT	55298
rs5743656	snp	A/G	0.0337553	0.125452	upstream-variant-2KB, downstream-variant-500B	IL18BP, RNF121	GRCh38.p7	11:71997914	TTCTCTTCCCCAGCT[A/G]TGGCTTCCCATGGTA	55298
rs5743657	snp	A/G	0.00517822	0.0506191	upstream-variant-2KB, downstream-variant-500B, utr-variant-5-prime	IL18BP, RNF121	GRCh38.p7	11:71998091	CAAAGCTCTTTTCAT[A/G]TGTAACAGTTCTGAG	55298
rs5792563	in-del	-/T	0.215747	0.247642	intron-variant	RNF121	GRCh38.p7	11:71948946	GCTGAACCTACCAGG[-/T]TTCATGAGCTAGCTA	55298
rs5792564	in-del	-/A			intron-variant	RNF121	GRCh38.p7	11:71950421	AACCCTGTCTCTACT[-/A]AAAAATACAAAAATT	55298
rs5792566	in-del	-/A	0.470908	0.117046	intron-variant	RNF121	GRCh38.p7	11:71991236	TTATTAAAAAAAAAA[-/A]TTAGCCAGATCTCAG	55298
rs6592447	snp	A/T	0.211516	0.24702	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71930047	GACTGGTGTATTAAA[A/T]TACCAGTGGTCCTTG	55298
rs6592448	snp	C/T	0.284995	0.247539	intron-variant	RNF121	GRCh38.p7	11:71958998	TGTTTTTAAGTGTGC[C/T]CTACCCTCTTAGCCT	55298
rs6592449	snp	C/T	0.284733	0.247575	intron-variant	RNF121	GRCh38.p7	11:71959176	TTTCTGTCAGATTCT[C/T]CCACCCAGGGTAAAG	55298
rs6592450	snp	C/T	0.383053	0.211653	intron-variant	RNF121	GRCh38.p7	11:71960120	TCTCTAGTTACTAAA[C/T]TTCCTTGAGCCTTTG	55298
rs6592451	snp	A/G	0.284995	0.247539	intron-variant	RNF121	GRCh38.p7	11:71963891	tctgttcttttgcag[A/G]taccacattgttatg	55298
rs6592452	snp	A/G	0.284733	0.247575	intron-variant	RNF121	GRCh38.p7	11:71968330	CTCGCAAAGTGCTGG[A/G]ATGACAGGTGTGAGC	55298
rs6592453	snp	C/G	0.284471	0.247612	intron-variant	RNF121	GRCh38.p7	11:71972185	AGAAAGCAATAAACA[C/G]TTTGCATGAACAGGT	55298
rs6592455	snp	A/G	0.284995	0.247539	intron-variant	RNF121	GRCh38.p7	11:71978495	ACCTTATCACTTTTC[A/G]TATGTCAGTTATTTT	55298
rs7102192	snp	A/G	0.322483	0.239262	intron-variant	RNF121	GRCh38.p7	11:71937123	TATCAGTGAGTCATC[A/G]GCACTGCTTTCTGCT	55298
rs7102523	snp	C/T	0.211516	0.24702	intron-variant	RNF121	GRCh38.p7	11:71987872	TGTGAGGGAATGAGA[C/T]GACACAGATGGGTGT	55298
rs7102639	snp	A/C/G	0.040671	0.13668	intron-variant	RNF121	GRCh38.p7	11:71958034	GGTGATTTTAAGCTT[A/C/G]GTATGAACCAGTTGT	55298
rs7103210	snp	C/G	0.357451	0.225731	intron-variant	RNF121	GRCh38.p7	11:71937920	CCTCTACTCCTCAGA[C/G]AAAAATCTGTAGGTA	55298
rs7106653	snp	A/G	0.215446	0.2476	intron-variant	RNF121	GRCh38.p7	11:71964800	GCTGTGTTTTAGTAC[A/G]AGTTAGCAACCTGTC	55298
rs7106730	snp	A/G	0.184521	0.241273	intron-variant	RNF121	GRCh38.p7	11:71938306	CATTTTACGTGTGTA[A/G]TCTCTTAATTTTTTT	55298
rs7106748	snp	A/C	0.283947	0.247685	intron-variant	RNF121	GRCh38.p7	11:71934757	GTAAACAGTGGGTTC[A/C]TATTCTAGACTagga	55298
rs7108458	snp	G/T	0	0	intron-variant	RNF121	GRCh38.p7	11:71976837	ggtttcattttgtgg[G/T]tttgattcttcattt	55298
rs7113436	snp	A/T	0.215144	0.247558	intron-variant	RNF121	GRCh38.p7	11:71978553	TTGTATGTGTGACTT[A/T]ATGCATTTTTAATCA	55298
rs7113520	snp	A/G	0.212122	0.247114	intron-variant	RNF121	GRCh38.p7	11:71980900	tgagatattttgtat[A/G]tattggaataaataa	55298
rs7114081	snp	A/T	0.0581099	0.160244	intron-variant	RNF121	GRCh38.p7	11:71993301	cagtgttctgcaaca[A/T]tttcactgtctaatt	55298
rs7114483	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71950773	ttcccctgcctcagc[C/G]tccccagtagctggg	55298
rs7115513	snp	A/T	0.211516	0.24702	intron-variant	RNF121	GRCh38.p7	11:71953449	AGATGCAATTTGTGA[A/T]TGTGAGTGCTGGGAT	55298
rs7121080	snp	A/G	0.215747	0.247642	intron-variant	RNF121	GRCh38.p7	11:71992889	CTGTTTATAAAAGTA[A/G]TATGTTCTCTTTGTA	55298
rs7121260	snp	A/G	0.357877	0.225527	intron-variant	RNF121	GRCh38.p7	11:71989520	TGGTGTAAGATCAAT[A/G]ATTTCTAGTGAGTTA	55298
rs7121292	snp	A/C	0.00438332	0.0466095	intron-variant	RNF121	GRCh38.p7	11:71964701	ctaggctggtctcgc[A/C]ctcctgaactcaagc	55298
rs7123536	snp	C/T	0.00358779	0.0422022	intron-variant	RNF121	GRCh38.p7	11:71939947	TAGAGTTATAAATTA[C/T]GTACAAGATGCCACA	55298
rs7124429	snp	G/T	0.0581099	0.160244	intron-variant	RNF121	GRCh38.p7	11:71993095	GAAAACAGTACATTG[G/T]ATCACTTTATTGACA	55298
rs7125718	snp	C/T	0.0399052	0.1355	intron-variant	RNF121	GRCh38.p7	11:71993380	actcattaccccttc[C/T]cacagccctggttta	55298
rs7126394	snp	A/G	0.215144	0.247558	intron-variant	RNF121	GRCh38.p7	11:71974383	ACCTACTCTGTTATA[A/G]CACTTATAATGAATT	55298
rs7128317	snp	A/G	0.284471	0.247612	intron-variant	RNF121	GRCh38.p7	11:71990321	TCATTGTCACCAGTT[A/G]GGGGAGGCAAGGACT	55298
rs7128346	snp	A/G	0.32955	0.237006	intron-variant	RNF121	GRCh38.p7	11:71966205	tgtatttttagtaga[A/G]acagggtttctccac	55298
rs7128974	snp	C/G	0.284733	0.247575	intron-variant	RNF121	GRCh38.p7	11:71965986	tcatttggcttcttt[C/G]aattatttgttcata	55298
rs7130215	snp	C/G	0.0622301	0.165053	intron-variant	RNF121	GRCh38.p7	11:71936904	GCACATAGCCCATAT[C/G]CATATATTTATTGAG	55298
rs7131230	snp	C/T	0.366885	0.220993	intron-variant	RNF121	GRCh38.p7	11:71990115	CGGAGTAATTTTCAG[C/T]CTCTGCACCAGTGAC	55298
rs7924516	snp	C/T	0.284995	0.247539	intron-variant	RNF121	GRCh38.p7	11:71956943	TTACGTCTGTCTTTC[C/T]CACTAGTCTGTGAGC	55298
rs7924834	snp	A/G	0.21695	0.247806	intron-variant	RNF121	GRCh38.p7	11:71933287	CCACTCTCAAGTCCT[A/G]TTTATCTGCCAAAAT	55298
rs7925196	snp	A/G	0.0599851	0.162463	intron-variant	RNF121	GRCh38.p7	11:71967167	tgagccaccgcgccc[A/G]gccAATATTTGTGTT	55298
rs7925411	snp	G/T	0.218151	0.247963	intron-variant	RNF121	GRCh38.p7	11:71967340	gtaataattATGTGG[G/T]ttttttttgtttttt	55298
rs7925604	snp	A/G	0.211516	0.24702	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71930210	CATGCCAGCATATGG[A/G]CAAAGACATCACAGG	55298
rs7925901	snp	C/T	0.284733	0.247575	intron-variant	RNF121	GRCh38.p7	11:71967072	gagacggggtttcac[C/T]ttgttagccaggatg	55298
rs7926550	snp	C/G	0.00318978	0.0398085	intron-variant	RNF121	GRCh38.p7	11:71985164	actcctgagctcaaa[C/G]aatcctcccacttca	55298
rs7929479	snp	C/T	0.0399052	0.1355	intron-variant	RNF121	GRCh38.p7	11:71981583	GGGAGTTAGGAGGCA[C/T]TGGAGAGAAGACTAG	55298
rs7931163	snp	A/G	0.0402882	0.136092	intron-variant	RNF121	GRCh38.p7	11:71986684	tgaggcagaagaatc[A/G]cttgaactcaggagg	55298
rs7931941	snp	C/T	0.408188	0.193589	intron-variant	RNF121	GRCh38.p7	11:71956558	GATGGCTAGTGATAT[C/T]GCTAGTTAATAGCAG	55298
rs7932163	snp	A/T	0.0600199	0.162504	intron-variant	RNF121	GRCh38.p7	11:71970818	AGCAACTACCAAGAC[A/T]GGGACTTACCTTGCC	55298
rs7932263	snp	A/G	0.0584853	0.160693	intron-variant	RNF121	GRCh38.p7	11:71940736	tgaggtaaaccagac[A/G]tgggaacagatggtt	55298
rs7937408	snp	A/G	0.184838	0.241358	intron-variant	RNF121	GRCh38.p7	11:71966904	gaatctcactctgtc[A/G]cccaggccggactgc	55298
rs7938496	snp	A/G	0.211516	0.24702	intron-variant	RNF121	GRCh38.p7	11:71984632	gggtctcactctgtc[A/G]cccaggctggagtgc	55298
rs7939435	snp	A/G	0.0240643	0.107019	intron-variant	RNF121	GRCh38.p7	11:71949345	attgcttaggcctgg[A/G]aagtcgacactgcag	55298
rs7940392	snp	A/G	0.215747	0.247642	intron-variant	RNF121	GRCh38.p7	11:71967017	gctgggactacaggc[A/G]cccgccaccgcgccc	55298
rs7942626	snp	A/G	0.215747	0.247642	intron-variant	RNF121	GRCh38.p7	11:71992803	ATGGGTAAATTAACA[A/G]CCAATCTGAGAAACG	55298
rs7943227	snp	A/G	0.38286	0.211774	intron-variant	RNF121	GRCh38.p7	11:71959675	GAATCTCATTCTGTC[A/G]CCCAGGACGGAGTGC	55298
rs7945374	snp	A/T	0.00318978	0.0398085	intron-variant	RNF121	GRCh38.p7	11:71985497	TTGTGATCAGTGCAA[A/T]CCCTGGAGAATAGAG	55298
rs7945535	snp	C/T	0.0596104	0.162024	intron-variant	RNF121	GRCh38.p7	11:71970473	ccagacaagcttggg[C/T]aatgcagggagaccc	55298
rs7948821	snp	A/G	0.284733	0.247575	intron-variant	RNF121	GRCh38.p7	11:71941439	ATACTTGTGACTTCA[A/G]tgtcaaacatttttc	55298
rs7949480	snp	C/T	0.284471	0.247612	intron-variant	RNF121	GRCh38.p7	11:71986542	GGAGGCTGAGGCGAG[C/T]GGATCATGTGGTCAG	55298

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