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
rs6643	snp	C/T	0.176751	0.239028	missense, synonymous-codon	RNF181	GRCh38.p7	2:85597128	TGTCCCTTGTGCCGC[C/T]ATGAGCTGCCCACTG	51255
rs14242	snp	A/G	0.240478	0.249819	utr-variant-3-prime, upstream-variant-2KB	VAMP5, RNF181	GRCh38.p7	2:85593289	GGCATGACAGGAAAT[A/G]CAGGGGTGCACATGT	51255
rs1049357	snp	A/C	0	0	utr-variant-3-prime, upstream-variant-2KB	VAMP5, RNF181	GRCh38.p7	2:85593312	GCTGCCCTCAAGGGC[A/C]AGTCTGTGGCATGAC	51255
rs1127974	snp	A/G	0.19218	0.243222	synonymous-codon, intron-variant	RNF181	GRCh38.p7	2:85596916	TTCCAGCTGCATTCT[A/G]CCCTGGCTAAGCAAG	51255
rs1562322	snp	A/G	0.239326	0.249772	upstream-variant-2KB	RNF181	GRCh38.p7	2:85594833	ATGTTTTACACGCTC[A/G]ATCATCCCCTCAATA	51255
rs2232738	snp	A/G	0.0325976	0.123435	upstream-variant-2KB, utr-variant-5-prime	RNF181	GRCh38.p7	2:85595493	GCCAGAAATCCCCGG[A/G]AATTCAGTCTTGGCT	51255
rs2232739	snp	G/T	0.0693013	0.172766	upstream-variant-2KB, utr-variant-5-prime	RNF181	GRCh38.p7	2:85595559	TCTCCATCATTGGCG[G/T]TAGTCTCTGGTCACC	51255
rs2232740	snp	C/T	0.0345262	0.126772	upstream-variant-2KB, utr-variant-5-prime	RNF181	GRCh38.p7	2:85595695	CTCTCAGCTCGTCAG[C/T]TTATTGGCCAGCGCC	51255
rs2232741	snp	C/T			utr-variant-5-prime	RNF181	GRCh38.p7	2:85595724	CCGCTAGGCCGCTAT[C/T]GAGCAGGGTCCGAGG	51255
rs2232742	snp	A/G/T	0.000764289	0.0195339	utr-variant-5-prime	RNF181	GRCh38.p7	2:85595740	GAGCAGGGTCCGAGG[A/G/T]CTGTGTCAGAAGGCT	51255
rs2232743	snp	C/T	1.78414e-05	0.0029867	missense	RNF181	GRCh38.p7	2:85595768	GCTGGGCAGCCATGG[C/T]GTCCTATTTCGATGA	51255
rs2232744	snp	G/T			synonymous-codon	RNF181	GRCh38.p7	2:85595769	CTGGGCAGCCATGGC[G/T]TCCTATTTCGATGAA	51255
rs2232745	snp	C/T	0.185032	0.242424	intron-variant	RNF181	GRCh38.p7	2:85596509	TCTGACTTTACATCC[C/T]CTTCCCCAGGTCACT	51255
rs2232747	snp	C/T	0.176614	0.238986	intron-variant	RNF181	GRCh38.p7	2:85596950	CTGCTTCTCTTCTTC[C/T]AGCTCTCACCGTGCC	51255
rs2232748	snp	C/G	0.464768	0.128121	intron-variant, missense	RNF181	GRCh38.p7	2:85596961	CTTCTAGCTCTCACC[C/G]TGCCCTGGGCCCAGT	51255
rs2232750	snp	C/T	0.239902	0.249796	intron-variant	RNF181	GRCh38.p7	2:85597345	CAGCAATGCAGACGC[C/T]AGAGGCCTGAAAACA	51255
rs2232751	snp	C/G/T			intron-variant	RNF181	GRCh38.p7	2:85597387	ATAATAGCTGCCCAT[C/G/T]CCCTCACCCATAGGC	51255
rs2289975	snp	A/G	0.000346395	0.0131559	synonymous-codon, missense	RNF181	GRCh38.p7	2:85597130	ATCAGTGGGCAGCTC[A/G]TAGCGGCACAAGGGA	51255
rs3755009	snp	G/T	0.338976	0.23363	intron-variant, upstream-variant-2KB	VAMP5, RNF181	GRCh38.p7	2:85593783	GGAGTGCAATGGCAC[G/T]ATCTCAGCTCACTGC	51255
rs3755010	snp	C/G	0.240765	0.249829	upstream-variant-2KB	RNF181	GRCh38.p7	2:85594403	GCCATATAGGCCAGG[C/G]AGGCAGTGCCTTCAG	51255
rs3755011	snp	G/T	0.240765	0.249829	upstream-variant-2KB	RNF181	GRCh38.p7	2:85594476	ATAAAGCCACACCAA[G/T]ACTGTGGAAACAGGG	51255
rs6742887	snp	A/G	0.0448719	0.142907	upstream-variant-2KB	RNF181	GRCh38.p7	2:85594081	CTCTGAACACTTCCC[A/G]CTCCTCAATTTCTCT	51255
rs7573200	snp	A/G	0.0275645	0.114116	intron-variant	RNF181	GRCh38.p7	2:85596045	CCGTTGGGCCGGCCT[A/G]GGGCAAGGGGATTGC	51255
rs10186164	snp	C/G	0.0279526	0.114869	upstream-variant-2KB, utr-variant-5-prime	RNF181	GRCh38.p7	2:85595400	TCGCAGAGGCCTCTA[C/G]CATCTGTACTGTCGA	51255
rs11541122	snp	A/G			synonymous-codon, intron-variant	RNF181	GRCh38.p7	2:85596832	CAAAAGACACACGGG[A/G]CACTTGAGCTCAGCC	51255
rs11541124	snp	C/T			missense, intron-variant	RNF181	GRCh38.p7	2:85596842	AAGTGCCCCGTGTGT[C/T]TTTTGGAATTTGAGG	51255
rs11688233	snp	A/T	0.0524604	0.153226	upstream-variant-2KB	RNF181	GRCh38.p7	2:85594591	CAGTTCCTTGCTGGG[A/T]AAAGTGAGCGCTACT	51255
rs17026482	snp	A/G	0.0162398	0.0886349	intron-variant	RNF181	GRCh38.p7	2:85596436	TACTAGCTGGGCAGC[A/G]TGTTTATTAATGTCC	51255
rs34716921	in-del	-/T			upstream-variant-2KB	RNF181	GRCh38.p7	2:85594258	CTCTCCCTCCCTCTT[-/T]CGACGGGGTCTATGT	51255
rs34772095	in-del	-/A	0.216349	0.247725	intron-variant	RNF181	GRCh38.p7	2:85596354	TCTGATAGCAGTTGT[-/A]AACTATTTCCCATCG	51255
rs35031968	in-del	-/AA			downstream-variant-500B	TMEM150A, RNF181	GRCh38.p7	2:85598140	AAAAAAAAAAAAAAA[-/AA]GCTGATAAACTAGCC	51255
rs35880310	in-del	-/G	0.375	0.216506	intron-variant	RNF181	GRCh38.p7	2:85596045	CCGTTGGGCCGGCCT[-/G]GGGCAAGGGGATTGC	51255
rs41290037	snp	C/T	0.0793507	0.182699	intron-variant, missense	RNF181	GRCh38.p7	2:85596955	TCTCTTCTTCTAGCT[C/T]TCACCGTGCCCTGGG	51255
rs56661114	snp	C/T	0.115438	0.210697	intron-variant, upstream-variant-2KB	VAMP5, RNF181	GRCh38.p7	2:85593676	TGCTTAGAGGACCAA[C/T]GAGACTGTAGATGCG	51255
rs57103456	in-del	-/A			downstream-variant-500B	TMEM150A, RNF181	GRCh38.p7	2:85598140	AAAAAAAAAAAAAAA[-/A]GCTGATAAACTAGCC	51255
rs57595370	snp	A/G	0.000399281	0.0141238	intron-variant	RNF181	GRCh38.p7	2:85596385	TGCTTTTTATCTAGT[A/G]AGCATCTACTAACTA	51255
rs60883970	in-del	-/CC	0.240478	0.249819	intron-variant, upstream-variant-2KB	VAMP5, RNF181	GRCh38.p7	2:85593467	GGGCTGCTTAAAAAG[-/CC]CATCACCCAAAGGAC	51255
rs72923021	snp	C/T	0.0524604	0.153226	upstream-variant-2KB	RNF181	GRCh38.p7	2:85594553	GTGGCAAGGGGAATT[C/T]AGGGTCAAGTGTGTA	51255
rs75720757	snp	A/G	0.0741063	0.177655	utr-variant-3-prime, downstream-variant-500B	RNF181	GRCh38.p7	2:85597689	AAGGCACCAGGCTGC[A/G]GTTTTCCTCCCTGCT	51255
rs78431533	snp	A/C	0.5	0	downstream-variant-500B	TMEM150A, RNF181	GRCh38.p7	2:85598121	AGCAAAACTCCGTCT[A/C]AAAAAAAAAAAAAAA	51255
rs79259438	snp	A/C	0.5	0	downstream-variant-500B	TMEM150A, RNF181	GRCh38.p7	2:85598124	AAAACTCCGTCTCAA[A/C]AAAAAAAAAAAAAAA	51255
rs79825049	snp	G/T	0.000399281	0.0141238	intron-variant	RNF181	GRCh38.p7	2:85596471	GATTATGGGGACAAA[G/T]AAAAAGCATAGTTTT	51255
rs111475577	snp	C/G	0.000399281	0.0141238	intron-variant	RNF181	GRCh38.p7	2:85596342	GTGCTGGGGCGGTCT[C/G]ATAGCAGTTGTAAAC	51255
rs111514784	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, utr-variant-5-prime	RNF181	GRCh38.p7	2:85595529	TCCAAAACAAATGAT[C/T]CCTCACCAGCCAGAT	51255
rs111827866	snp	A/C			utr-variant-3-prime	RNF181	GRCh38.p7	2:85597581	AGGTTTCTTTACCCA[A/C]CCTGAGGCTGTATTG	51255
rs113521042	snp	A/C/G	0.0005438	0.0164807	utr-variant-5-prime	RNF181	GRCh38.p7	2:85595750	CGAGGGCTGTGTCAG[A/C/G]AGGCTGGGCAGCCAT	51255
rs114139079	snp	G/T	0.0107246	0.0724382	downstream-variant-500B	RNF181	GRCh38.p7	2:85597921	AGGTCAGGAGTTCGA[G/T]ACCTTCCTGACCAAC	51255
rs116048888	snp	C/G	0.0337553	0.125452	intron-variant, upstream-variant-2KB	VAMP5, RNF181	GRCh38.p7	2:85593475	TAAAAAGCCCATCAC[C/G]CAAAGGACTCCACCC	51255
rs117260196	snp	C/T	0.00123658	0.0248346	intron-variant	RNF181	GRCh38.p7	2:85597207	CTTAAGTGGAGGGGT[C/T]GTAATGGGCTCCCTG	51255
rs139155037	snp	A/T	0.00280301	0.0373316	missense	RNF181	GRCh38.p7	2:85596601	CCACCAGCTGCCAAG[A/T]CTGTGGTTGAGAACC	51255
rs139301266	snp	A/G	0.000486483	0.0155886	missense	RNF181	GRCh38.p7	2:85597168	CTTATGAGGAGCACA[A/G]ACGAGATAAGGTAGG	51255
rs139962566	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF181	GRCh38.p7	2:85594840	GGGATGATCGAGCGT[A/G]TAAAACATACATCAG	51255
rs141263353	snp	A/G	1.67066e-05	0.00289016	synonymous-codon, missense	RNF181	GRCh38.p7	2:85597163	CGACACTTATGAGGA[A/G]CACAGACGAGATAAG	51255
rs142112842	snp	C/T	3.57168e-05	0.00422577	intron-variant	RNF181	GRCh38.p7	2:85597234	CCTGAGTCCTGTCCC[C/T]GCTGCCATCACTTCC	51255
rs144178796	snp	A/C	0.00835141	0.0640778	upstream-variant-2KB	RNF181	GRCh38.p7	2:85593979	CCTGCCTCGGCCTTC[A/C]GAAGTGCTAGAATTG	51255
rs145644511	snp	A/G	0.0023933	0.0345097	upstream-variant-2KB	RNF181	GRCh38.p7	2:85595241	TAACACATAAGAAAT[A/G]CGCAGGAATCAAACG	51255
rs145964756	snp	G/T	1.70443e-05	0.00291923	missense	RNF181	GRCh38.p7	2:85597445	CCTTCTTTCCTTCAG[G/T]CTCGAAAACAGCAGC	51255
rs146076109	snp	C/T	0.00199481	0.0315187	upstream-variant-2KB	RNF181	GRCh38.p7	2:85594627	AAACCAGAATAAGCC[C/T]GAGTTGTGTGGAGCT	51255
rs146552045	snp	A/G	6.59609e-05	0.00574248	missense	RNF181	GRCh38.p7	2:85597126	CCTGTCCCTTGTGCC[A/G]CTATGAGCTGCCCAC	51255
rs147576123	snp	A/G	0.00159617	0.0282053	intron-variant	RNF181	GRCh38.p7	2:85595988	AGTACGGGCGGCGAG[A/G]CTGAGGGGTGTGGGG	51255
rs148260133	snp	A/G	9.94233e-05	0.00704995	missense, synonymous-codon	RNF181	GRCh38.p7	2:85597149	CTGCCCACTGATGAC[A/G]ACACTTATGAGGAGC	51255
rs148575905	snp	A/C/G/T	0.000181906	0.00953541	synonymous-codon, missense	RNF181	GRCh38.p7	2:85597501	TGGAGCCATGTACAC[A/C/G/T]TGAGGAGGTTGGGGC	51255
rs149289789	snp	C/T	0.000153988	0.00877328	synonymous-codon	RNF181	GRCh38.p7	2:85596550	ATGGACTTTGAAGAC[C/T]TGGGGTTGGTAGTAG	51255
rs149659522	snp	C/T	9.98951e-05	0.00706665	stop-gained, synonymous-codon	RNF181	GRCh38.p7	2:85597469	CAGCAGCAGCAACAC[C/T]GACTGGAGAACCTCC	51255
rs149752231	snp	A/G	0.0189856	0.0955633	upstream-variant-2KB	RNF181	GRCh38.p7	2:85595147	GTAACAGTCCCATGA[A/G]CTGGTTGAGGCCCCA	51255
rs181466368	snp	C/T			upstream-variant-2KB	RNF181	GRCh38.p7	2:85595012	GGTATCAGACACGGG[C/T]GTTTCTAAAGCTCCT	51255
rs182365001	snp	C/T	0.000313069	0.0125075	intron-variant	RNF181	GRCh38.p7	2:85596798	GCCTGTAGCAGCTCT[C/T]CTGATCAGCACTCCT	51255
rs183777284	snp	A/G	0.000116452	0.00762971	missense	RNF181	GRCh38.p7	2:85597470	AGCAGCAGCAACACC[A/G]ACTGGAGAACCTCCA	51255
rs183827000	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	RNF181	GRCh38.p7	2:85597950	ACATGGTGAAACCCC[A/G]TTTCTACTAAAAATA	51255
rs184147857	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	VAMP5, RNF181	GRCh38.p7	2:85593802	TCAGCTCACTGCAAA[C/T]TCCACCTCCTGGGTT	51255
rs185444882	snp	C/T	0.000399281	0.0141238	intron-variant	RNF181	GRCh38.p7	2:85596812	TCCTGATCAGCACTC[C/T]TTCCTAAAGAGCTCA	51255
rs187426485	snp	C/T	0.000798403	0.0199641	intron-variant	RNF181	GRCh38.p7	2:85597392	AGCTGCCCATCCCCT[C/T]ACCCATAGGCCTTCA	51255
rs187615860	snp	C/G/T	1.66263e-05	0.00288321	missense, synonymous-codon	RNF181	GRCh38.p7	2:85596549	GATGGACTTTGAAGA[C/G/T]TTGGGGTTGGTAGTA	51255
rs188488585	snp	C/T			downstream-variant-500B	RNF181	GRCh38.p7	2:85597991	CTGGGCATGGTGGCA[C/T]GCACCTGTAATCCCA	51255
rs188834614	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	RNF181	GRCh38.p7	2:85594351	CAGGCGTGAGCCACC[A/G]TGTCCAGCCTGAATT	51255
rs189107010	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, upstream-variant-2KB	VAMP5, RNF181	GRCh38.p7	2:85593288	AACATGTGCACCCCT[A/G]CATTTCCTGTCATGC	51255
rs190150720	snp	A/G	0.00107683	0.0231787	intron-variant, synonymous-codon	RNF181	GRCh38.p7	2:85597032	AGAAGAGTGGCAGTT[A/G]GGAGCAGGGGAGGGT	51255
rs190696311	snp	C/G	6.60786e-05	0.0057476	missense	RNF181	GRCh38.p7	2:85596641	CAGTCATCAGAGGCT[C/G]TCAGGCTGGTGAGGA	51255
rs191848600	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	TMEM150A, RNF181	GRCh38.p7	2:85598167	AGCCTGCACCCTCCT[C/T]CCACTGCAATGTCTA	51255
rs192279066	snp	C/G	0.000399281	0.0141238	downstream-variant-500B	RNF181	GRCh38.p7	2:85597801	AGGCAAAATGTGTCA[C/G]GGTCTGGTACCCAGT	51255
rs192770569	snp	A/C	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	VAMP5, RNF181	GRCh38.p7	2:85593478	AAAGCCCATCACCCA[A/C]AGGACTCCACCCCTG	51255
rs193186735	snp	A/C	3.44929e-05	0.00415274	intron-variant	RNF181	GRCh38.p7	2:85597430	CCCCTGCCCAGCATG[A/C]CTTCTTTCCTTCAGG	51255
rs199659104	snp	C/T	2.18133e-05	0.00330245	utr-variant-5-prime	RNF181	GRCh38.p7	2:85595733	CGCTATCGAGCAGGG[C/T]CCGAGGGCTGTGTCA	51255
rs200828041	snp	A/G	1.97124e-05	0.0031394	intron-variant	RNF181	GRCh38.p7	2:85595873	GCGGGGCTTGGGGAT[A/G]GGGTCCAACCAGCAG	51255
rs201174906	snp	C/T	0.00199792	0.0315431	missense, intron-variant	RNF181	GRCh38.p7	2:85596903	ATCACCTTTTCCATT[C/T]CAGCTGCATTCTGCC	51255
rs201303606	snp	C/G	4.96734e-05	0.0049834	utr-variant-3-prime, missense	RNF181	GRCh38.p7	2:85597520	GGAGGTTGGGGCTGA[C/G]TGCTGGCCCTCTGCG	51255
rs201423825	snp	A/G	1.75953e-05	0.00296603	missense	RNF181	GRCh38.p7	2:85595832	GACGCGAACCAACAT[A/G]CTGCTGGAGCTCGCA	51255
rs201474398	snp	C/T	0.0019981	0.0315445	missense	RNF181	GRCh38.p7	2:85595771	GGGCAGCCATGGCGT[C/T]CTATTTCGATGAACA	51255
rs201698985	snp	A/C			intron-variant, synonymous-codon	RNF181	GRCh38.p7	2:85597047	GGGAGCAGGGGAGGG[A/C]GGTTATCAGCTTATG	51255
rs202048391	snp	C/G	0.00031295	0.0125051	splice-donor-variant, intron-variant	RNF181	GRCh38.p7	2:85596932	CCCTGGCTAAGCAAG[C/G]TACTGCTTCTCTTCT	51255
rs367566914	in-del	-/C	0.00159617	0.0282053	upstream-variant-2KB	RNF181	GRCh38.p7	2:85595203	AGTTGGGGAGGCTTG[-/C]CCCCACCCTTTATTA	51255
rs367593390	snp	C/T	0.000153988	0.00877328	missense	RNF181	GRCh38.p7	2:85595831	AGACGCGAACCAACA[C/T]GCTGCTGGAGCTCGC	51255
rs367835972	snp	C/G	1.72012e-05	0.00293263	intron-variant	RNF181	GRCh38.p7	2:85597197	GGGGCTGATGCTTAA[C/G]TGGAGGGGTCGTAAT	51255
rs367932660	snp	G/T			upstream-variant-2KB	RNF181	GRCh38.p7	2:85595132	AGCAACGGGCTGAAG[G/T]TAACAGTCCCATGAG	51255
rs368059230	snp	C/T	0.000153988	0.00877328	synonymous-codon	RNF181	GRCh38.p7	2:85595793	CGATGAACACGACTG[C/T]GAGCCGTCGGACCCT	51255
rs369313522	snp	A/G	1.64727e-05	0.00286986	intron-variant	RNF181	GRCh38.p7	2:85596793	GCAGAGCCTGTAGCA[A/G]CTCTCCTGATCAGCA	51255
rs369431907	snp	A/G	0.00755907	0.0610114	downstream-variant-500B	TMEM150A, RNF181	GRCh38.p7	2:85598117	CAAGAGCAAAACTCC[A/G]TCTCAAAAAAAAAAA	51255
rs369656195	snp	C/G	0.000120295	0.00775453	intron-variant	RNF181	GRCh38.p7	2:85596515	TTTACATCCCCTTCC[C/G]CAGGTCACTTTTCAA	51255
rs370114662	snp	C/T	1.71343e-05	0.00292692	intron-variant	RNF181	GRCh38.p7	2:85597439	AGCATGCCTTCTTTC[C/T]TTCAGGCTCGAAAAC	51255
rs370554005	snp	A/G	1.68238e-05	0.00290028	missense	RNF181	GRCh38.p7	2:85597171	ATGAGGAGCACAGAC[A/G]AGATAAGGTAGGGGC	51255

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