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
rs754706	snp	C/T	0.38934	0.207568	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154032	AGGTAAATATGGACC[C/T]GTATGTATCTCCTGC	114804
rs754707	snp	C/T	0.443464	0.15834	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76154067	CCCGCACCTGACATC[C/T]ATGGCTCTGAGGCCC	114804
rs754708	snp	C/T	0.444666	0.15686	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153888	AGTCCTCCCCCTCCC[C/T]CCAGTGGAAGAAATG	114804
rs881502	snp	C/T	0.444067	0.1576	synonymous-codon, downstream-variant-500B, nc-transcript-variant	RNF157	GRCh38.p7	17:76156285	AGTGAGAATCTCACC[C/T]TGTCGTCATCTGGAG	114804
rs894544	snp	C/T	0.144969	0.226867	intron-variant	RNF157	GRCh38.p7	17:76155375	TCGTGACAGCAAACC[C/T]AAACCTTCTTCAGAA	114804
rs920713	snp	C/G	0.180383	0.240111	intron-variant	RNF157	GRCh38.p7	17:76178804	CCCCCAAGTTTTAGG[C/G]AGCAGAGGTTATTTT	114804
rs1108127	snp	C/T	0.0240643	0.107019	intron-variant	RNF157	GRCh38.p7	17:76204757	AGTACACTGTATGCA[C/T]CTTATTTCTtttctt	114804
rs1376356	snp	C/T	0.305258	0.243817	intron-variant	RNF157	GRCh38.p7	17:76166425	CTTTGGCTGTGCACA[C/T]TGCTCTTTTGTGGCA	114804
rs1465960	snp	C/T	0.401392	0.198948	utr-variant-3-prime, upstream-variant-2KB, intron-variant	RNF157, FOXJ1, RNF157-AS1	GRCh38.p7	17:76143183	CCTCAGTCCCATGTC[C/T]AAGGCATACCTAGGT	114804
rs1551104	snp	C/T	0.0154538	0.0865337	intron-variant	RNF157	GRCh38.p7	17:76167284	AATAGAAAAGTTTAA[C/T]GTTGCCAAGCAAGAG	114804
rs1868821	snp	A/G	0.4628	0.13121	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153608	CCACAGAGCAAGGAC[A/G]TAGGAGGAAGAAGGA	114804
rs1868822	snp	A/G	0.442655	0.159323	intron-variant, nc-transcript-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76153443	AGCAGATGTCATCCT[A/G]TTGCTTCTGCTTTAG	114804
rs1868827	snp	C/T	0.16618	0.23553	intron-variant	RNF157	GRCh38.p7	17:76178936	CCTTGGAAATCTCAT[C/T]TCTAGATTAAAAAGC	114804
rs1947284	snp	G/T	0	0	intron-variant	RNF157	GRCh38.p7	17:76159834	GTGATTTTTTTTCCT[G/T]ACTTTTACTTTTATG	114804
rs2028602	snp	A/G	0.00716266	0.059414	intron-variant	RNF157	GRCh38.p7	17:76159204	TGGGATAACCTTCAC[A/G]CAAGCAGCTCTGGGA	114804
rs2278824	snp	C/T	0.448708	0.151707	intron-variant	RNF157	GRCh38.p7	17:76167409	ACCCTTTACCTTTTC[C/T]CTTCAAATTGTGCCA	114804
rs2278825	snp	A/G	0.315758	0.241197	intron-variant	RNF157	GRCh38.p7	17:76167397	TTCCCTTCAAATTGT[A/G]CCATCTTGGTATAGT	114804
rs2278826	snp	C/T	0.433963	0.169285	intron-variant	RNF157	GRCh38.p7	17:76166916	AAGGGGCTGCTCGGA[C/T]GCTTGAAGGCCATGC	114804
rs2289602	snp	A/C	2.2677e-05	0.00336719	missense, nc-transcript-variant	RNF157	GRCh38.p7	17:76173759	CACCTCCCCAAGAAC[A/C]CGTGAAGACTCTGAG	114804
rs2289603	snp	C/T	0.305829	0.243694	synonymous-codon, nc-transcript-variant	RNF157	GRCh38.p7	17:76167740	AGCTAAAGTCCACTA[C/T]AATGTTGAGTTCACC	114804
rs2289604	snp	C/T	0.126219	0.217206	intron-variant	RNF157	GRCh38.p7	17:76160700	AACCAAAATTAAAAG[C/T]TAGACAACAAATAGT	114804
rs2289605	snp	C/G	0.431029	0.17242	intron-variant	RNF157	GRCh38.p7	17:76160671	GTGTTTTTTTAAAAA[C/G]TATTTACAATGTGTG	114804
rs2289606	snp	G/T	0.321053	0.23969	intron-variant	RNF157	GRCh38.p7	17:76160616	TGCCATAGTTCATAT[G/T]GAATAAAACAGTAGA	114804
rs2290244	snp	C/T	0.0792508	0.182605	intron-variant	RNF157	GRCh38.p7	17:76162486	GAAATCGTAAGCCAG[C/T]GTCCAGAAATTTAGC	114804
rs2410923	snp	A/G	0.0607341	0.163335	intron-variant	RNF157	GRCh38.p7	17:76231287	tacaggcgtgcagcc[A/G]tgcccggccTCttgc	114804
rs2585734	snp	A/G	0	0			GRCh38.p7	17:76179722	AGATCTCTGGTTTTA[A/G]GTTGAAATAAGATAC	114804
rs2585735	snp	C/T	0.431916	0.171483			GRCh38.p7	17:76153219	TGATTGTTTCTCCCA[C/T]AGAATATTTGCTTCT	114804
rs2585736	snp	C/G	0.0337553	0.125452			GRCh38.p7	17:76152680	AGCAGCAGACAGAAA[C/G]GGCTCTAGGGAAACA	114804
rs2585737	snp	A/C	0.438246	0.16451			GRCh38.p7	17:76151543	TCCGGGTTTCACGAC[A/C]GAAATTGTCCTTCAC	114804
rs2585738	snp	C/T	0.457969	0.138741			GRCh38.p7	17:76150652	TTAACTGGCATCCTC[C/T]GTCAGTAGTTGGGTG	114804
rs2598424	snp	A/G	0.436692	0.166271			GRCh38.p7	17:76152997	ACTCAGGTCTCATAA[A/G]GAAGGAAATCATAAT	114804
rs2598425	snp	A/G	0.417683	0.185425			GRCh38.p7	17:76146810	TGGTCGGCCTTGTCC[A/G]CTGAACAGGTCCTCC	114804
rs2598426	snp	G/T	0.179425	0.239831			GRCh38.p7	17:76146141	GAAGTGAGCCCACAG[G/T]AGGCTGTGGAGGATT	114804
rs2598427	snp	C/T	0.458545	0.137872			GRCh38.p7	17:76143613	ATGGAGAGGGGGGCC[C/T]GTCGTCCAACCCTCT	114804
rs2598449	snp	A/G	0	0			GRCh38.p7	17:76179784	TCTTGGTCCCAAGAA[A/G]GCATTAGTTTTCTTT	114804
rs3075396	in-del	-/GA	0.375	0.216506	intron-variant	RNF157	GRCh38.p7	17:76238419	GTTAAACTTTTAAAA[-/GA]CTGGTAGAGAGGAGA	114804
rs3744036	snp	A/T	0.268936	0.249282	intron-variant	RNF157, RNF157-AS1	GRCh38.p7	17:76145404	CCTTTGGCCAAATCC[A/T]GATGGTGTCTCCAGC	114804
rs3816427	snp	A/G	0.320575	0.239832	intron-variant	RNF157	GRCh38.p7	17:76163060	ATATTTTCCCTTCCC[A/G]TCTTTTTCCTTGCCA	114804
rs3859178	snp	C/T	0.499673	0.0127754	intron-variant	RNF157	GRCh38.p7	17:76217694	GTGAGTGACGTGTTT[C/T]TCCTGGTAACAAATA	114804
rs3859179	snp	C/T	0.0607341	0.163335	intron-variant	RNF157	GRCh38.p7	17:76231538	CCTAACCTCAGGTGA[C/T]CTTCTGGCCTTGGCC	114804
rs3859180	snp	C/T	0.409382	0.192607	intron-variant	RNF157	GRCh38.p7	17:76238167	TCCTTTCAGGACTAA[C/T]ACTGTAATCCCATAA	114804
rs3859181	snp	A/G	0.499793	0.0101816	intron-variant	RNF157	GRCh38.p7	17:76238577	TGTTAAGTCCCACAT[A/G]TGAAAGAGCGGTGAA	114804
rs4102459	snp	A/G	0	0	intron-variant	RNF157	GRCh38.p7	17:76226235	TGGATATCACTGAAG[A/G]AGATAGGAAGCCGGA	114804
rs4102460	snp	A/G	0	0	intron-variant	RNF157	GRCh38.p7	17:76226222	AGAAGATAGGAAGCC[A/G]GACTCCACTGCTTAC	114804
rs4102461	snp	A/C	0	0	intron-variant	RNF157	GRCh38.p7	17:76226217	ATAGGAAGCCGGACT[A/C]CACTGCTTACGTTGC	114804
rs4143087	snp	C/G	0	0	intron-variant	RNF157	GRCh38.p7	17:76175899	TGTTTCATTGCCACA[C/G]ttatcatcaaatata	114804
rs4316786	snp	A/G	0.0685596	0.171987	intron-variant	RNF157	GRCh38.p7	17:76205427	ataagccgccatgcc[A/G]ggcACATTTTAGTTC	114804
rs4505373	snp	G/T	0.481396	0.0946345	intron-variant	RNF157	GRCh38.p7	17:76208511	aaaagcttagaacaa[G/T]cagccctggcaaaaa	114804
rs4525514	snp	C/T	0.474091	0.11083	intron-variant	RNF157	GRCh38.p7	17:76198278	GAGAGCCTGTTGATA[C/T]AGGGACATTCTCTTA	114804
rs4788915	snp	C/T	0.141258	0.225111	intron-variant	RNF157	GRCh38.p7	17:76162720	TTTGGTAACCAAGGA[C/T]TACCGATTCATAATG	114804
rs4788916	snp	C/T	0.428333	0.175206	intron-variant	RNF157	GRCh38.p7	17:76173142	ATACAAAAAATTAGC[C/T]GGACGTGGTGGCGGG	114804
rs4789246	snp	A/C	0.111928	0.208413	intron-variant	RNF157	GRCh38.p7	17:76157883	ATGGGCCTCCCGACA[A/C]CCCCCACTTACCCCC	114804
rs4789247	snp	C/T	0.428786	0.174744	intron-variant	RNF157	GRCh38.p7	17:76173012	AAAAAGAAGGCTGGG[C/T]GCGGTGGCTCACGCC	114804
rs4789248	snp	A/G	0.0260105	0.111035	intron-variant	RNF157	GRCh38.p7	17:76176954	GGTTCTGCGCAGCCC[A/G]TCTGGGGCTGCGCCC	114804
rs4789249	snp	C/T	0.452597	0.146474	intron-variant	RNF157	GRCh38.p7	17:76187477	gcatgagccacggcg[C/T]ctggccAGGATTTTA	114804
rs4789250	snp	A/G	0.477515	0.103619	intron-variant	RNF157	GRCh38.p7	17:76194754	GGCACGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	114804
rs4789251	snp	C/T	0.48178	0.0936921	intron-variant	RNF157	GRCh38.p7	17:76202737	AGTGGCCAATCGAGG[C/T]TTCAAACAAGTCACA	114804
rs4789252	snp	A/C	0.247621	0.249989	intron-variant	RNF157	GRCh38.p7	17:76223011	ttctcctgcctcagc[A/C]ttccgagtagctggg	114804
rs4789253	snp	A/G	0.247905	0.249991	intron-variant	RNF157	GRCh38.p7	17:76224510	CTTTAGATCACAAAA[A/G]TAAGAAGAAAACTAG	114804
rs4789254	snp	A/T	0.25801	0.249872	intron-variant	RNF157	GRCh38.p7	17:76224682	GGTCTTACGCCACAC[A/T]TGAAATACACTAACA	114804
rs4789255	snp	A/G	0.499713	0.0119774	intron-variant	RNF157	GRCh38.p7	17:76224830	catgtagcccagccc[A/G]tggggcgtgggttgt	114804
rs4789256	snp	C/T	0.247905	0.249991	intron-variant	RNF157	GRCh38.p7	17:76225040	agccgggtatggtgg[C/T]gggcatctgtaatcc	114804
rs5822121	in-del	-/GT			intron-variant	RNF157	GRCh38.p7	17:76182482	TGTGTGTGTGTGTGT[-/GT]ATCAATCACATGTCC	114804
rs5822122	in-del	-/AG	0.495999	0.0445491	intron-variant	RNF157	GRCh38.p7	17:76238418	AGTTAAACTTTTAAA[-/AG]ACTGGTAGAGAGGAG	114804
rs6416850	snp	C/T	0.329084	0.237162	intron-variant	RNF157	GRCh38.p7	17:76201162	TTAAAAATGAAAACA[C/T]GTTCACTGGAAAAAA	114804
rs6501860	snp	C/G	0.329084	0.237162	intron-variant	RNF157	GRCh38.p7	17:76200904	GAGCTCCCTGACTCT[C/G]CTCCTCCCCATGCTT	114804
rs6501861	snp	C/T	0.330714	0.236612	intron-variant	RNF157	GRCh38.p7	17:76201251	agcactttgggaggc[C/T]gaggcaggaggattg	114804
rs6501862	snp	C/G	0.258288	0.249863	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213651	ctaatgaattaacca[C/G]tgcctggcagcccct	114804
rs6501863	snp	A/G	0.258288	0.249863	intron-variant, upstream-variant-2KB	RNF157	GRCh38.p7	17:76213858	aaggactggttcaga[A/G]agcttccaaacaggg	114804
rs6501864	snp	C/T	0.25801	0.249872	intron-variant	RNF157	GRCh38.p7	17:76222480	aattttaaaaaaTCA[C/T]ATGGGGAGGAAGAAT	114804
rs6501865	snp	A/G	0.247053	0.249983	intron-variant	RNF157	GRCh38.p7	17:76223440	tgatccatccgcctc[A/G]gcctcccaaagtgct	114804
rs6501867	snp	C/G	0.25045	0.25	intron-variant	RNF157	GRCh38.p7	17:76226266	CTTCACTGCCCAGCT[C/G]TAAACTAAAGGAATG	114804
rs6501868	snp	A/G	0.499713	0.0119774	intron-variant	RNF157	GRCh38.p7	17:76226409	ACCATCTGGGGGGGC[A/G]CCTTATTAGTCTCCT	114804
rs6501869	snp	A/C	0.248755	0.249997	intron-variant	RNF157	GRCh38.p7	17:76235083	ttatatgcatagtaa[A/C]ttttaaaatagggta	114804
rs7207415	snp	C/T			intron-variant	RNF157	GRCh38.p7	17:76222179	gaagcaaccccgtct[C/T]tactaaaaatacaaa	114804
rs7208373	snp	C/T	0.0681886	0.171594	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76150583	CAAGTAAGGGGTTGA[C/T]CAGGGTAGAGCTGCC	114804
rs7210049	snp	C/T	0.464416	0.128553	intron-variant	RNF157	GRCh38.p7	17:76226239	GCTTCCTATCTTCTT[C/T]AGTGATATCCACTTC	114804
rs7210745	snp	C/T	0.249603	0.25	intron-variant	RNF157	GRCh38.p7	17:76234554	cattttttaaaatta[C/T]agccatcctagtggg	114804
rs7210831	snp	A/G	0.25801	0.249872	intron-variant	RNF157	GRCh38.p7	17:76217865	CTTTGCAGGCTTTAA[A/G]AAGTCACATCATACA	114804
rs7214563	snp	C/T	0.279195	0.248289	intron-variant	RNF157	GRCh38.p7	17:76218195	aaagaaagaaaggca[C/T]ccaggcaaaaagtca	114804
rs7217334	snp	C/T	0.258288	0.249863	intron-variant	RNF157	GRCh38.p7	17:76221798	gtgaggtataatgtg[C/T]ccgacatatgtcctt	114804
rs7220727	snp	C/G	0.24932	0.249999	intron-variant	RNF157	GRCh38.p7	17:76237170	CCCAAGTCTCAACTT[C/G]AAATCTGCCATTCTT	114804
rs7221261	snp	A/G	0.111928	0.208413	intron-variant	RNF157	GRCh38.p7	17:76172556	agatcgcagtgagcc[A/G]agatcgtgccattgc	114804
rs7225367	snp	A/G	0.419296	0.183954	upstream-variant-2KB	RNF157	GRCh38.p7	17:76241453	GTGTTTTTTTTCCTG[A/G]GAGAGTGGACTGATC	114804
rs7225664	snp	C/T	0.0349115	0.127424	intron-variant	RNF157	GRCh38.p7	17:76234740	tgagcatatgagttc[C/T]ttatatattctagat	114804
rs7225796	snp	A/C	0.0836354	0.186609	intron-variant	RNF157	GRCh38.p7	17:76206787	ctcaaaaaacaaaca[A/C]agaaaaCAGTGAAGA	114804
rs7225855	snp	C/T	0.499703	0.0121769	intron-variant	RNF157	GRCh38.p7	17:76228324	CCTTCTTCCTTGTGG[C/T]GCTCTCAGAACCCTT	114804
rs7359559	snp	A/G	0	0	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151689	CATGATCCTGTGTAA[A/G]GCATTACCTAGATTT	114804
rs7359560	snp	A/G	0	0	intron-variant, utr-variant-3-prime	RNF157, RNF157-AS1	GRCh38.p7	17:76151730	CATGAGGAGGAATAA[A/G]GGGCACTCTGACAAC	114804
rs7502444	snp	A/G			intron-variant	RNF157	GRCh38.p7	17:76199474	gcccaggctggtctt[A/G]aactcctgggctcaa	114804
rs7502723	snp	A/T			intron-variant	RNF157	GRCh38.p7	17:76199589	aaaaaaaaaaaaaaa[A/T]aaagaaCAGCTGGCA	114804
rs8067190	snp	A/T	0.0298908	0.118541	intron-variant	RNF157	GRCh38.p7	17:76176426	GCAAATTAAAAAAAA[A/T]TTTTTTTCTGCTCTT	114804
rs8067947	snp	C/T	0.488302	0.0755777	intron-variant	RNF157	GRCh38.p7	17:76199070	ACAATGGGTATTCCA[C/T]AGAATGTAAATGATT	114804
rs8068111	snp	C/T	0.0429648	0.14013	intron-variant	RNF157	GRCh38.p7	17:76220331	atatattaagcttca[C/T]caggataataagggc	114804
rs8068137	snp	C/T	0.487241	0.0788465	intron-variant	RNF157	GRCh38.p7	17:76169108	atttccttcctttta[C/T]attctctgttctctg	114804
rs8068290	snp	C/T	0.247905	0.249991	intron-variant	RNF157	GRCh38.p7	17:76220435	atgctagtaaaccaa[C/T]tcattattttggaaa	114804
rs8068421	snp	A/G	0.0995161	0.199636	intron-variant	RNF157	GRCh38.p7	17:76199020	CAGGGACTGCATTTC[A/G]TCGGTATTTCTAGTG	114804
rs8068624	snp	A/T	0.442926	0.158996	intron-variant	RNF157	GRCh38.p7	17:76220658	tacaaatttattatt[A/T]ttttttttttagtta	114804
rs8070392	snp	C/T	0.49823	0.0296997	intron-variant	RNF157	GRCh38.p7	17:76210945	gagcagctgggatta[C/T]aggggtgtgccacca	114804
rs8070711	snp	C/G	0.158302	0.232576	intron-variant	RNF157	GRCh38.p7	17:76240034	CTCGAAGACCGTTTC[C/G]GAGCGTCCGCAACCA	114804

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