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
rs376900	snp	A/G	0.495671	0.0463237	intron-variant	CASS4	GRCh38.p7	20:56451479	AGGGGGATGCATAGG[A/G]GTTTGGTGGATGGAA	57091
rs386274	snp	A/C	0.432797	0.170544	intron-variant	CASS4	GRCh38.p7	20:56455025	AAATAGGACTGACTC[A/C]GTTCCTCTTTGACAT	57091
rs401897	snp	C/T	0.408359	0.193449	intron-variant	CASS4	GRCh38.p7	20:56454702	AAACCTATCTTGGAA[C/T]AAAGGTTAGATGAAA	57091
rs442481	snp	A/G	0.496105	0.0439572	intron-variant	CASS4	GRCh38.p7	20:56451476	GTCAGGGGGATGCAT[A/G]GGGGTTTGGTGGATG	57091
rs718022	snp	A/G	0.114036	0.209795	intron-variant	CASS4	GRCh38.p7	20:56428409	TGAGTCCTGCATTGG[A/G]CAGGAACACCCAGGC	57091
rs735780	snp	A/G	0.33533	0.234987	intron-variant	CASS4	GRCh38.p7	20:56434091	GGTAATGCACAGGGT[A/G]GATTAGGGTACAAGG	57091
rs911159	snp	A/G	0.245005	0.24995	synonymous-codon	CASS4	GRCh38.p7	20:56437262	TCTGGAGCAACACGT[A/G]CCAGAAAGCGAGGGT	57091
rs911163	snp	A/T	0.499673	0.0127754	upstream-variant-2KB	CASS4	GRCh38.p7	20:56410057	CCTAGAAAAAACAAC[A/T]TGTGAATTATAGCAT	57091
rs927172	snp	A/G	0.5	0	intron-variant	CASS4	GRCh38.p7	20:56436376	TATATATATATATGT[A/G]TATATATATATATAG	57091
rs927173	snp	C/G	0.326506	0.238006	intron-variant	CASS4	GRCh38.p7	20:56439671	TGGGTGACTGACCGG[C/G]ACCCTGTCTTAAAAA	57091
rs927174	snp	A/C	0.0685596	0.171987	intron-variant	CASS4	GRCh38.p7	20:56440110	GCTACAAGACATAGA[A/C]CCAGACAGTTGTTAC	57091
rs1321458	snp	C/T	0.477041	0.104654	intron-variant	CASS4	GRCh38.p7	20:56440000	TGGTGTGGAGAAGGC[C/T]TGAATGGTGAGTAGC	57091
rs1884910	snp	C/G	0.499703	0.0121769	intron-variant	CASS4	GRCh38.p7	20:56451685	AGGCTCAAAAGAATC[C/G]TGAAGGACCTTGAGT	57091
rs1923117	snp	A/G	0.251296	0.249997	intron-variant	CASS4	GRCh38.p7	20:56457537	ATATTTTAATATTAA[A/G]GCAAAAAATAAAATA	57091
rs2024964	snp	G/T	0.293551	0.246177	intron-variant	CASS4	GRCh38.p7	20:56454195	GTCttttgttttttt[G/T]ttgttgttgttcttg	57091
rs2064860	snp	G/T	0.490782	0.0672626	intron-variant	CASS4	GRCh38.p7	20:56435906	aaaattagctgggca[G/T]agtagcgcatgcctg	57091
rs2064861	snp	A/C	0.479502	0.0991411	intron-variant	CASS4	GRCh38.p7	20:56432903	GGGAAGATTTCTGTG[A/C]CGCCCCTGCCCACAC	57091
rs2064862	snp	C/G	0.488786	0.0740357	intron-variant	CASS4	GRCh38.p7	20:56432901	GAAGATTTCTGTGAC[C/G]CCCCTGCCCACACTT	57091
rs2145282	snp	A/G			missense	CASS4	GRCh38.p7	20:56437266	GAGCAACACGTGCCA[A/G]AAAGCGAGGGTTGGT	57091
rs2426624	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	CASS4	GRCh38.p7	20:56411799	TATTCATTAGGTACC[A/G]TGAGCAAAGACCAGG	57091
rs2426625	snp	G/T	0.000399281	0.0141238	intron-variant	CASS4	GRCh38.p7	20:56421038	AGCACCTCTAAAAAT[G/T]ACCATAGAAAGATGG	57091
rs2426626	snp	G/T	0.0535932	0.154675	intron-variant	CASS4	GRCh38.p7	20:56421135	GCTTTGAATTCTTCC[G/T]GGTCAATCAAATGGA	57091
rs2426627	snp	A/G	0.0244538	0.107838	intron-variant	CASS4	GRCh38.p7	20:56448877	Acatcatcactggcc[A/G]tcagagaaatgcaaa	57091
rs2426628	snp	A/G	0.0763149	0.179815	intron-variant	CASS4	GRCh38.p7	20:56451641	TGGCAGACCAGGTGG[A/G]GTCAGCGTGGTGGAA	57091
rs2870737	snp	A/G	0	0	intron-variant	CASS4	GRCh38.p7	20:56436362	TGTGTGTGTGTGTGT[A/G]TATATATATATGTAT	57091
rs2870738	snp	A/G	0.480046	0.0983462	synonymous-codon, intron-variant	CASS4	GRCh38.p7	20:56453111	ATTAAAGAAAAATAG[A/G]GCAAATATCTGTGGA	57091
rs2870739	snp	A/T	0.498525	0.0271165	intron-variant	CASS4	GRCh38.p7	20:56457447	GTAGGATTTGGGAGA[A/T]GTTGGTTCCATTTTC	57091
rs2870740	snp	A/G	0.498158	0.0302955	intron-variant	CASS4	GRCh38.p7	20:56457607	TCTGGAAATGTTGAG[A/G]GTTCTGATATATCTC	57091
rs2870741	snp	A/G	0.498182	0.0300969	intron-variant	CASS4	GRCh38.p7	20:56457614	ATGTTGAGAGTTCTG[A/G]TATATCTCTGATACT	57091
rs3044223	snp	A/G	0.5	0	intron-variant	CASS4	GRCh38.p7	20:56436374	TGTATATATATATAT[A/G]TATATATATATATAT	57091
rs3219626	in-del	-/ACAC	0.5	0	intron-variant	CASS4	GRCh38.p7	20:56416529	CACACACACACACAC[-/ACAC]GGAAGTAAACAGAAT	57091
rs3746621	snp	A/G	0.000166937	0.00913457	synonymous-codon	CASS4	GRCh38.p7	20:56437364	CGCTGCAGACAGGCC[A/G]TGCCCCCCATTCCTG	57091
rs3746622	snp	A/G	9.93888e-05	0.00704872	missense	CASS4	GRCh38.p7	20:56445966	TCCCAGGTGTATGAC[A/G]TGCCTACCCAGCACC	57091
rs3746623	snp	C/G	0.493842	0.0551477	synonymous-codon	CASS4	GRCh38.p7	20:56458420	TGAACACTGCCGGCT[C/G]TACTTTGGGGCGCTC	57091
rs3746624	snp	C/T	0.474213	0.110582	synonymous-codon	CASS4	GRCh38.p7	20:56458579	GAGGGACGTGCGCAA[C/T]GAGATCCTCCGTGGC	57091
rs3746625	snp	C/T	0.493702	0.055762	synonymous-codon	CASS4	GRCh38.p7	20:56458591	CAACGAGATCCTCCG[C/T]GGCAGCAGTCACCTC	57091
rs3746626	snp	A/G	0.494374	0.0527379	synonymous-codon	CASS4	GRCh38.p7	20:56458657	GAATGCCGTGCTCAC[A/G]TACCCCAGCCCTGCC	57091
rs3761206	snp	A/G	0.179744	0.239925	upstream-variant-2KB	CASS4	GRCh38.p7	20:56411164	AATGCTGTCTGACAA[A/G]AAGATAGCGGTAAGC	57091
rs3761207	snp	A/G	0.408017	0.193729	upstream-variant-2KB	CASS4	GRCh38.p7	20:56411319	TGAGAGGCTGAGGTG[A/G]GTGGATCACTTGAGG	57091
rs3787390	snp	A/G	0.498832	0.0241331	intron-variant	CASS4	GRCh38.p7	20:56440292	GCTGACTCGGAGCAG[A/G]GCTTTGCTGAGGTTT	57091
rs3787393	snp	C/T	0.465788	0.126237	intron-variant	CASS4	GRCh38.p7	20:56455978	tgcatggctgggccc[C/T]gctctcagaattttt	57091
rs3838042	in-del	-/C	0.495708	0.0461266	intron-variant	CASS4	GRCh38.p7	20:56451507	GAAAAGAAAGGGTTG[-/C]CAAGGGCATTTAGAG	57091
rs3970972	snp	A/G	0.486984	0.079614	intron-variant	CASS4	GRCh38.p7	20:56436360	tgtgtgtgtgtgtgt[A/G]tatatatatatatgt	57091
rs4811694	snp	A/G	0.408359	0.193449	intron-variant	CASS4	GRCh38.p7	20:56454332	AGGAGATAATTTGCT[A/G]CTTTCAGCCCCGACC	57091
rs4811695	snp	A/T	0.498503	0.0273153	intron-variant	CASS4	GRCh38.p7	20:56457805	AGATCATTTGAGATC[A/T]GGGGTTCAAAACCAA	57091
rs4811696	snp	C/T	0.498459	0.0277128	intron-variant	CASS4	GRCh38.p7	20:56457996	CTCCAGCCTGGAAGA[C/T]AAAGGAAAACTCTGT	57091
rs4811697	snp	A/C	0.498568	0.0267188	utr-variant-3-prime	CASS4	GRCh38.p7	20:56458800	AGCTTCACACCCACA[A/C]CTTGTGCAACTCTGC	57091
rs5842113	in-del	-/C	0.498927	0.0231381	intron-variant	CASS4	GRCh38.p7	20:56435314	GCTTTATTTATGAAA[-/C]GTATGAACAAAGGTT	57091
rs6014721	snp	A/T	0.0134968	0.0810323	upstream-variant-2KB	CASS4	GRCh38.p7	20:56410742	gactccgtctcaaaa[A/T]aaataaataaataaa	57091
rs6014722	snp	A/T	0.149665	0.228982	intron-variant	CASS4	GRCh38.p7	20:56414777	tggtgaaaccccatc[A/T]ctagtaaaaatacaa	57091
rs6014723	snp	C/G	0.0356815	0.128715	intron-variant	CASS4	GRCh38.p7	20:56418509	gttttctagatcact[C/G]aggctgctgtgcaac	57091
rs6014724	snp	A/G	0.271162	0.249103	intron-variant	CASS4	GRCh38.p7	20:56423488	ATATTTTTGTTTAGA[A/G]AGTTATATTCTATTC	57091
rs6014726	snp	C/T	0	0	intron-variant	CASS4	GRCh38.p7	20:56427738	GATATTTATAGTATA[C/T]GCAGTTTTTAAAATG	57091
rs6014727	snp	A/C	0.467946	0.122472	intron-variant	CASS4	GRCh38.p7	20:56434127	TGCAGTCTCATTCAC[A/C]GTGGGTGGAGGTGTG	57091
rs6014728	snp	C/T	0.275999	0.248644	intron-variant	CASS4	GRCh38.p7	20:56436752	TTTAGCCCGGGGTGG[C/T]GGCACGCATGTGTAG	57091
rs6014729	snp	A/G	0.256619	0.249912	intron-variant	CASS4	GRCh38.p7	20:56436758	CCGGGGTGGCGGCAC[A/G]CATGTGTAGTCCCAG	57091
rs6014730	snp	A/G	0.498871	0.0237351	intron-variant	CASS4	GRCh38.p7	20:56438160	AGCATAGTAGCACAC[A/G]TGTGTAGTCCCAACT	57091
rs6014731	snp	A/G	0.0170251	0.090679	intron-variant	CASS4	GRCh38.p7	20:56440285	CTGAGCAGCTGACTC[A/G]GAGCAGAGCTTTGCT	57091
rs6014732	snp	C/G	0.136847	0.222927	intron-variant	CASS4	GRCh38.p7	20:56440696	AGTTTACTATTGAAA[C/G]TTAACTTTGAAAAAT	57091
rs6014733	snp	C/T	0.0498117	0.149749	intron-variant	CASS4	GRCh38.p7	20:56442087	ACTGTTTTCCCATGG[C/T]AAATTCACAGGCTTG	57091
rs6014734	snp	C/T	0.00716266	0.059414	intron-variant	CASS4	GRCh38.p7	20:56456128	TTCTCAGTGGAGGCC[C/T]GGGGCACCGTTGGCC	57091
rs6024864	snp	A/G	0.486464	0.0811471	intron-variant	CASS4	GRCh38.p7	20:56413446	GGGAGGCCAAGGCAG[A/G]TGGATCACTTGAGGC	57091
rs6024868	snp	C/T	0.0236746	0.106192	intron-variant	CASS4	GRCh38.p7	20:56419466	CCCCCACACCACCCC[C/T]gctcaggctggagta	57091
rs6024870	snp	A/G	0.103794	0.20279	intron-variant	CASS4	GRCh38.p7	20:56422512	ATATTAAAGCATGTC[A/G]ATCTGGGTAACACCC	57091
rs6024871	snp	A/G	0.0298908	0.118541	intron-variant	CASS4	GRCh38.p7	20:56422636	CCTCCTCAAAGCCCC[A/G]TTAGTAGGCAGTGCC	57091
rs6024875	snp	A/G	0.303938	0.244112	intron-variant	CASS4	GRCh38.p7	20:56433036	TCATTCATTAATTCA[A/G]CAAGTAGCTAAAGAT	57091
rs6024877	snp	C/T	0.409552	0.192466	intron-variant	CASS4	GRCh38.p7	20:56438952	AGACTGAGAAGAACA[C/T]GCTCCAGGCATAGTT	57091
rs6024878	snp	A/G	0.0166325	0.0896639	intron-variant	CASS4	GRCh38.p7	20:56440549	ATGCCACTCAATACA[A/G]TGACAGGCTCCTACA	57091
rs6024879	snp	C/T	0.471863	0.115225	intron-variant	CASS4	GRCh38.p7	20:56442504	CTACAGATGCTACGT[C/T]ACAGCTCTGTAACTT	57091
rs6024880	snp	C/T	0.0941369	0.195465	intron-variant	CASS4	GRCh38.p7	20:56444435	CCTCTCCTCCAGGCC[C/T]TGTCTTGCTTACCAG	57091
rs6024881	snp	G/T	0.144296	0.226554	intron-variant	CASS4	GRCh38.p7	20:56445633	tgggcccaagaatct[G/T]catgttaacctgctt	57091
rs6024882	snp	A/G	0.481396	0.0946345	intron-variant	CASS4	GRCh38.p7	20:56449108	gccatcccattactg[A/G]gtatatacccaaagg	57091
rs6024883	snp	G/T	0.132751	0.2208	intron-variant	CASS4	GRCh38.p7	20:56450321	gagccaccacgcccg[G/T]ctGAGAAGTCTCTTT	57091
rs6024884	snp	C/G	0.482425	0.0951571	intron-variant	CASS4	GRCh38.p7	20:56450456	AGATTTCTACCATTA[C/G]AGCATCATGACCAAA	57091
rs6024885	snp	C/T	0.00557542	0.0525036	intron-variant	CASS4	GRCh38.p7	20:56451606	AAACAGCTTGGGTGG[C/T]TGGACCTGTAAGCAG	57091
rs6024887	snp	C/T	0.0182019	0.0936463	intron-variant	CASS4	GRCh38.p7	20:56453287	AAGTAAAATTCTTGA[C/T]GAAATCTTATTAACA	57091
rs6024888	snp	A/G	0.451483	0.148002	intron-variant	CASS4	GRCh38.p7	20:56454981	TGTAGGGGCTCTGCA[A/G]GGTTGTTGTGGGTGG	57091
rs6024889	snp	A/G	0.0138799	0.0821421	intron-variant	CASS4	GRCh38.p7	20:56456178	ATTGCGTGGTGAACC[A/G]TTCAGCATCCCAGAA	57091
rs6024890	snp	C/G	0.00438332	0.0466095	intron-variant	CASS4	GRCh38.p7	20:56456616	ctgacctcaagtgac[C/G]ctcctgcctcagcct	57091
rs6064392	snp	G/T	0.110872	0.20771	upstream-variant-2KB	CASS4	GRCh38.p7	20:56409712	TAGAGTCCTTCTGAC[G/T]TAGTTCCCTTGAACT	57091
rs6069737	snp	C/T	0.104859	0.203554	intron-variant	CASS4	GRCh38.p7	20:56420643	caagcagtcctcctg[C/T]ctcagcctcctaaag	57091
rs6069740	snp	A/G	0.0209421	0.100162	intron-variant	CASS4	GRCh38.p7	20:56429946	CACTTACAAGAGATG[A/G]AAACCCTGTatttat	57091
rs6069746	snp	C/T	0.32627	0.238082	intron-variant	CASS4	GRCh38.p7	20:56440475	AAGACCACTTCACAA[C/T]CAGTTAAGTTTTCTG	57091
rs6069749	snp	C/T	0.0810805	0.184299	intron-variant	CASS4	GRCh38.p7	20:56446519	CTTAACATTGATTAT[C/T]TCTGGGGGAAGAAAT	57091
rs6069751	snp	C/T	0.498908	0.0233371	intron-variant	CASS4	GRCh38.p7	20:56449391	gcatgttctcactca[C/T]aggtgggaaatgaac	57091
rs6069753	snp	A/G	0.444314	0.157297	intron-variant	CASS4	GRCh38.p7	20:56450706	GAGGTGCTAAGGTGC[A/G]GTGTTATGAACACAC	57091
rs6069754	snp	A/C/T	1.65252e-05	0.00287443	missense, intron-variant	CASS4	GRCh38.p7	20:56453032	CTCCCCAAAGAGAAA[A/C/T]TGAATCACACCAAAA	57091
rs6069755	snp	A/C/T	4.97302e-05	0.00498624	missense, intron-variant	CASS4	GRCh38.p7	20:56453062	AGAGTACCCCTTCCA[A/C/T]TAAGCAAAGGGAAGA	57091
rs6092314	snp	C/G	0.138586	0.226022	intron-variant	CASS4	GRCh38.p7	20:56440769	CATCAACCATTTGAG[C/G]CCTTGCTTGTGCAGG	57091
rs6092315	snp	A/G	0.00398564	0.0444627	intron-variant	CASS4	GRCh38.p7	20:56442455	TCTGTGGCTGACGCT[A/G]TTCTTTCTGATGAAC	57091
rs6092316	snp	A/C	0.465683	0.126415	intron-variant	CASS4	GRCh38.p7	20:56450284	CTGCCTCAGCCTCCC[A/C]AAGTGTTGGGATTAC	57091
rs6099133	snp	A/T	0.00159617	0.0282053	upstream-variant-2KB	CASS4	GRCh38.p7	20:56410247	gaccttgggcaagtt[A/T]atccatccttcCTTT	57091
rs6099136	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB	CASS4	GRCh38.p7	20:56410782	tatggtacctgaatt[A/G]tatcttaatataata	57091
rs6099137	snp	G/T	0.00159617	0.0282053	upstream-variant-2KB	CASS4	GRCh38.p7	20:56410912	TTATCTGCTATCGCC[G/T]GCAGCATGCCAATTA	57091
rs6099138	snp	A/G	0.000399281	0.0141238	intron-variant	CASS4	GRCh38.p7	20:56421435	ggtgtggtagtccac[A/G]cctgtaatcccagca	57091
rs6099143	snp	C/T	0.000399281	0.0141238	intron-variant	CASS4	GRCh38.p7	20:56432275	AAAGCTTTCAGATTA[C/T]TGTTTTTTACTGAAC	57091
rs6099144	snp	A/G	0.14665	0.227637	intron-variant	CASS4	GRCh38.p7	20:56433272	agtgacatttaagat[A/G]agcctgaaaggatgt	57091
rs6099145	snp	A/T	0.493013	0.058691	intron-variant	CASS4	GRCh38.p7	20:56434573	TCCCAAGTAGCTGGG[A/T]CTACAGGTGCACGCC	57091
rs6099146	snp	A/G	0.0685596	0.171987	intron-variant	CASS4	GRCh38.p7	20:56434798	AAAATTGTGTGTTTC[A/G]TATTATGCCATTAGA	57091
rs6099147	snp	A/C	0.104504	0.2033	intron-variant	CASS4	GRCh38.p7	20:56436542	ttacagatgaggaaa[A/C]tgaggctctaatagg	57091

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