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
rs1122389	snp	C/T	0.340077	0.233208	intron-variant	KLHL38	GRCh38.p7	8:123646881	GCCAAGTTTGTGTCA[C/T]GCCCAGTGATCCTCT	340359
rs4367519	snp	C/T	0.209084	0.246629	upstream-variant-2KB	KLHL38	GRCh38.p7	8:123654189	ATTTCCCACCATCTG[C/T]CTGGCGGGATCGCTG	340359
rs4374971	snp	C/T	0.439641	0.162899	upstream-variant-2KB	KLHL38	GRCh38.p7	8:123654047	CTTGGGAATTCTAGC[C/T]GTCTGTAAACAGGTT	340359
rs4439107	snp	C/T	0.0372196	0.131242	intron-variant	KLHL38	GRCh38.p7	8:123646448	GGACAAACTGAGGCA[C/T]AGAAAGATGTTTAAC	340359
rs4496951	snp	C/T	0.440195	0.162252	upstream-variant-2KB	KLHL38	GRCh38.p7	8:123654874	CCATGCATTTTTTTT[C/T]CTTTGCTCCTAGTAC	340359
rs4871402	snp	A/C	0.336702	0.234484	intron-variant	KLHL38	GRCh38.p7	8:123648207	ATCTTTCAGTTTAGA[A/C]CATTGAGGCTCTGAG	340359
rs4871403	snp	C/T	0.334412	0.235318	intron-variant	KLHL38	GRCh38.p7	8:123648597	CTTCAGCTTTGGGTA[C/T]GGCTTTAAAAATAGA	340359
rs4871404	snp	C/T	0.346147	0.230772	intron-variant	KLHL38	GRCh38.p7	8:123649734	GGGGCTCAGGGGTTG[C/T]GATGTGGGCGGAGGA	340359
rs4871405	snp	A/G	0.164219	0.234823	intron-variant	KLHL38	GRCh38.p7	8:123650532	CCTTCACAATGGTTG[A/G]TGTTCAACATAACTC	340359
rs6470169	snp	C/T	0.440195	0.162252	upstream-variant-2KB	KLHL38	GRCh38.p7	8:123654918	ACATCCACCCTGTCT[C/T]CTCTGGAGCAGCCCC	340359
rs6470170	snp	C/T	0.440195	0.162252	upstream-variant-2KB	KLHL38	GRCh38.p7	8:123655082	TGTGGTAATCTAGCT[C/T]CATGAGACACTTACA	340359
rs7004851	snp	C/T	0.456214	0.141336	upstream-variant-2KB	KLHL38	GRCh38.p7	8:123655712	TAGAGTGGAAGTCTC[C/T]GGGCAGCAGGAATCT	340359
rs7386562	snp	C/T	0.331787	0.236348	missense	KLHL38	GRCh38.p7	8:123652634	TTGTCAGTGGCAATA[C/T]GTGCCTCCCCCGTAT	340359
rs7386679	snp	A/G	0.128976	0.218754	intron-variant	KLHL38	GRCh38.p7	8:123649665	AGCCCAGCCAGGCCA[A/G]CCTCATCTCCACAGA	340359
rs7386841	snp	C/G	0.155325	0.23138	utr-variant-3-prime	KLHL38	GRCh38.p7	8:123645023	TGAGAGAGAGGAAGA[C/G]AGAGGGGAGACTGAG	340359
rs7387179	snp	A/T	0.497776	0.0332724	intron-variant	KLHL38	GRCh38.p7	8:123649455	AAGCCATCACCACCC[A/T]TGCCTGGAACTCTAG	340359
rs7387544	snp	C/T	0.375626	0.216144	synonymous-codon	KLHL38	GRCh38.p7	8:123652552	CTGGCTCTGCAAGTA[C/T]GAGGAGCAGGCCTCA	340359
rs7387792	snp	A/G	0.331473	0.236352	synonymous-codon	KLHL38	GRCh38.p7	8:123652633	ATTGTCAGTGGCAAT[A/G]TGTGCCTCCCCCGTA	340359
rs7387855	snp	C/T	0.326748	0.237938	upstream-variant-2KB, intron-variant	KLHL38	GRCh38.p7	8:123652971	TCAGCAAGAGTCAAA[C/T]CTTTCTCAGCTGCAT	340359
rs7388119	snp	C/T	0.229136	0.249128	intron-variant	KLHL38	GRCh38.p7	8:123649803	TTGCATGAGGACTGA[C/T]GCCCGCCCCTAGCCA	340359
rs7463896	snp	A/G	0.41507	0.187755	upstream-variant-2KB, intron-variant	KLHL38	GRCh38.p7	8:123653335	ATCTGTTATTGAGTA[A/G]CAGATGTCTAAACCT	340359
rs7464171	snp	A/G	0.356811	0.226034	intron-variant	KLHL38	GRCh38.p7	8:123648095	CAAAAAATAAAATAA[A/G]GTAAGATTACCAGCA	340359
rs7464207	snp	G/T	0.33693	0.2344	intron-variant	KLHL38	GRCh38.p7	8:123648220	GAACATTGAGGCTCT[G/T]AGAGGTCAAATGACA	340359
rs9642868	snp	A/T	0.199873	0.244923	intron-variant	KLHL38	GRCh38.p7	8:123648102	TAAAATAAGGTAAGA[A/T]TACCAGCACTATTAA	340359
rs10094484	snp	C/T	0.151334	0.229706	intron-variant	KLHL38	GRCh38.p7	8:123649130	CTTGAAGCTTAAACT[C/T]TGAGTTTTATTCTCA	340359
rs10109736	snp	A/T	0.173709	0.238075	intron-variant	KLHL38	GRCh38.p7	8:123651529	GTGTGGGTGTGTCCA[A/T]GCACACATACTCATG	340359
rs10505438	snp	A/G	0.277867	0.248442	intron-variant	KLHL38	GRCh38.p7	8:123649679	AACCTCATCTCCACA[A/G]ATATCCATCCCTCAA	340359
rs10505439	snp	C/T	0.264632	0.249571	intron-variant	KLHL38	GRCh38.p7	8:123649864	CTCTGTCTTGCAACT[C/T]CATTGTCCTGCTTTC	340359
rs10956142	snp	A/G	0.164546	0.234942	upstream-variant-2KB	KLHL38	GRCh38.p7	8:123654109	TTCTGGGCCACAGTG[A/G]AGGTGGCAGGTGGTC	340359
rs11779866	snp	C/T	0.144918	0.226843	missense	KLHL38	GRCh38.p7	8:123645974	TCTTTCATGTCCGCA[C/T]ATTTGACAAATTTGT	340359
rs11780509	snp	C/T	0.375984	0.215935	missense	KLHL38	GRCh38.p7	8:123651890	TGACTGACCAGACTC[C/T]TCCCTGAGCTGACAG	340359
rs11784175	snp	A/T	0.201176	0.245186	missense	KLHL38	GRCh38.p7	8:123651873	AGAAGATGTAGACAT[A/T]GTGACTGACCAGACT	340359
rs11784192	snp	C/T	0.33083	0.236572	missense	KLHL38	GRCh38.p7	8:123651927	CCCCCAGCACATAGA[C/T]GCTGCGGTGCAAGGT	340359
rs11786734	snp	A/G	0.357664	0.225629	intron-variant	KLHL38	GRCh38.p7	8:123646164	GCACGTGGGATGTTG[A/G]GCTAACCTGCCAAGG	340359
rs11991744	snp	A/C	0.334642	0.235236	intron-variant	KLHL38	GRCh38.p7	8:123647089	CAGAAGTAGTAATTA[A/C]GAGGGTGAACTAGGA	340359
rs11994199	snp	G/T	0.415727	0.187175	intron-variant	KLHL38	GRCh38.p7	8:123651010	TTTAGATATATATTT[G/T]TCTCATCAAATGAAG	340359
rs13252050	snp	C/T	0.336017	0.234736	intron-variant	KLHL38	GRCh38.p7	8:123647311	GCTTGGAACATGTTT[C/T]TCTTTTAATGAGAAA	340359
rs13261088	snp	A/G			intron-variant	KLHL38	GRCh38.p7	8:123649993	TCTGACTCCGGCTTC[A/G]GGAGGTGCAGGAGCT	340359
rs13261337	snp	A/C	0	0	intron-variant	KLHL38	GRCh38.p7	8:123649992	CTCTGACTCCGGCTT[A/C]AGGAGGTGCAGGAGC	340359
rs13261403	snp	C/T			intron-variant	KLHL38	GRCh38.p7	8:123650072	Acccaccccacccct[C/T]cccctcctcttttat	340359
rs13261937	snp	A/C	0	0	intron-variant	KLHL38	GRCh38.p7	8:123650191	TAACCCTGGCACTCT[A/C]TCTGATTCTCTCTGG	340359
rs13262236	snp	A/C			intron-variant	KLHL38	GRCh38.p7	8:123650307	atgatagctgatgag[A/C]taaaaaaaatcgcta	340359
rs13270650	snp	A/T	0.356811	0.226034	intron-variant	KLHL38	GRCh38.p7	8:123648936	TAAACTATATTCGAA[A/T]GAGTAGAATGTTTAT	340359
rs16898671	snp	C/T	0.226889	0.248929	synonymous-codon	KLHL38	GRCh38.p7	8:123645970	CCGGTCTTTCATGTC[C/T]GCACATTTGACAAAT	340359
rs16898680	snp	A/T	0.0154538	0.0865337	intron-variant	KLHL38	GRCh38.p7	8:123649694	GATATCCATCCCTCA[A/T]GAAGGTTCCAGGATT	340359
rs16898685	snp	C/G	0.207253	0.246318	intron-variant	KLHL38	GRCh38.p7	8:123650420	CAAGCTTGCTCTAGA[C/G]TGGTTTAGGGCATCC	340359
rs16898686	snp	C/T	0.207253	0.246318	intron-variant	KLHL38	GRCh38.p7	8:123651075	CTTTGTTATGTATTA[C/T]TTTTGCACAAAAAAA	340359
rs16898687	snp	C/T	0.308908	0.242961	intron-variant	KLHL38	GRCh38.p7	8:123651232	GTACGTATTTGTGTT[C/T]GTGCATATGTATAAA	340359
rs16898689	snp	A/G	0.204747	0.24587	synonymous-codon	KLHL38	GRCh38.p7	8:123651655	TTTCACAGCGACTGC[A/G]GGGTGGAGCACCCCC	340359
rs16898691	snp	C/G	0.145825	0.227261	missense	KLHL38	GRCh38.p7	8:123651747	CCATGAGCTCCTGCC[C/G]TTCTCCAATCCCCCC	340359
rs16898693	snp	C/T	0.00353811	0.0419111	missense	KLHL38	GRCh38.p7	8:123651999	GGCTCTGCCATTGGC[C/T]GGTCTGTTTGCTGTA	340359
rs28742115	snp	A/G	0.00852895	0.0647436	synonymous-codon	KLHL38	GRCh38.p7	8:123652417	GAGCTCCTTCAGGTC[A/G]GCCGATGCGGCCACC	340359
rs34300449	snp	A/G	0.0107246	0.0724382	upstream-variant-2KB	KLHL38	GRCh38.p7	8:123654211	GGATCGCTGGGGAGA[A/G]CTGTGATTTCCTCCT	340359
rs34489649	in-del	-/A			downstream-variant-500B, utr-variant-3-prime	KLHL38	GRCh38.p7	8:123645283	TCTTTACTAAAACGC[-/A]AAAATTAGCTGGACT	340359
rs34568618	snp	A/G			intron-variant	KLHL38	GRCh38.p7	8:123650254	GCCACATTGGAAGGA[A/G]AGTTGTCTTGGGTCA	340359
rs34762234	in-del	-/G			intron-variant	KLHL38	GRCh38.p7	8:123648661	AAGAGGCTGGGGCAA[-/G]GGATAACAAAGGATG	340359
rs34792899	snp	A/G/T	0.0562307	0.157967	intron-variant	KLHL38	GRCh38.p7	8:123646210	AGTGGGGGCTGGCAC[A/G/T]CAAATCTGCCTGACT	340359
rs55686719	snp	A/G			intron-variant	KLHL38	GRCh38.p7	8:123651037	GAAGATAAACTCTGT[A/G]CATAGGGATGGTATT	340359
rs56151564	snp	A/G	0.147991	0.228242	upstream-variant-2KB	KLHL38	GRCh38.p7	8:123655550	TCCAAAACTTGGTTT[A/G]TGTATCACTTCTCTG	340359
rs56194946	in-del	-/AGAGAA/AGAGAG/AGAGAGAG/AGAGAGAT	0	0	utr-variant-3-prime	KLHL38	GRCh38.p7	8:123645056	GAGAGAGAGAGAGAG[lengthTooLong]GGGCAGAGAGAGGCA	340359
rs58763139	snp	A/G	0.254385	0.249962	intron-variant	KLHL38	GRCh38.p7	8:123649421	AAGAAAAAAATCTTC[A/G]CTGGAACTGACCGAG	340359
rs60409169	in-del	-/GACAGA/GAGA			downstream-variant-500B, utr-variant-3-prime	KLHL38	GRCh38.p7	8:123645480	AGAGAGAGAGAGAGA[-/GACAGA/GAGA]CAGACAGAGATAGGG	340359
rs61730395	snp	G/T	0.00026519	0.0115119	missense	KLHL38	GRCh38.p7	8:123651779	ATGGAGAAGATGAAG[G/T]TCTTATGGGCAGTGC	340359
rs61730397	snp	C/T	0.0802918	0.183573	synonymous-codon	KLHL38	GRCh38.p7	8:123652354	CACCTTTTCCTCCTC[C/T]CCACAGAGCCCATCA	340359
rs61732636	snp	A/C/G	0.00390194	0.0439976	missense	KLHL38	GRCh38.p7	8:123651825	GGGCCACCAGCATGG[A/C/G]CTCCCCCAGCCTCCA	340359
rs61741356	snp	A/C/T	0.0111499	0.0738294	missense	KLHL38	GRCh38.p7	8:123652128	GTTTGCAGTCTGGGA[A/C/T]GGTGGTGCCACACAA	340359
rs61910691	snp	A/G	0.000915408	0.0213744	synonymous-codon	KLHL38	GRCh38.p7	8:123652831	GCTCACATCAGTCAG[A/G]ATCCTGCTTTGCCTT	340359
rs61910739	snp	C/T	0.0813175	0.184516	missense	KLHL38	GRCh38.p7	8:123652884	AGTCAGAAGAGAAGT[C/T]GTGGTCTTTGAAGAG	340359
rs62518568	snp	C/T	0.0372196	0.131242	intron-variant	KLHL38	GRCh38.p7	8:123650212	TTCTCTCTGGACCAG[C/T]GGTGTCCAATCTTTT	340359
rs62518569	snp	A/G	0.324855	0.23853	intron-variant	KLHL38	GRCh38.p7	8:123650576	AAGTACATCTCGTGG[A/G]TGCTTCTGATTGTCT	340359
rs62518570	snp	A/G	0.0376037	0.131863	intron-variant	KLHL38	GRCh38.p7	8:123651324	TATGCATGTGCACAC[A/G]TATGCATGTTGGCAT	340359
rs66970129	snp	C/T	0.307671	0.243257	intron-variant	KLHL38	GRCh38.p7	8:123649767	TTGCTCCCGGTAGCC[C/T]GAGAAGGGGGCTGAT	340359
rs71505429	multinucleotide-polymorphism	AT/GC	0	0	missense	KLHL38	GRCh38.p7	8:123652633	ATTGTCAGTGGCAAT[AT/GC]GTGCCTCCCCCGTAT	340359
rs72140477	in-del	-/CA			downstream-variant-500B, utr-variant-3-prime	KLHL38	GRCh38.p7	8:123645478	AGAGAGAGAGAGAGA[-/CA]GACAGACAGAGATAG	340359
rs72711231	snp	C/T	0.139095	0.224054	missense	KLHL38	GRCh38.p7	8:123645963	GCATCCTCCGGTCTT[C/T]CATGTCCGCACATTT	340359
rs72711243	snp	A/G	0.209084	0.246629	upstream-variant-2KB	KLHL38	GRCh38.p7	8:123654973	AGTCCCCAGCATCAG[A/G]CCCTTCAGTGGCTCC	340359
rs73324207	snp	A/G	0.00279162	0.0372561	upstream-variant-2KB	KLHL38	GRCh38.p7	8:123653958	CGGCAAAAATAGATC[A/G]GGAGGAGCGGCTTCT	340359
rs73324208	snp	A/T	0.0232847	0.105357	upstream-variant-2KB	KLHL38	GRCh38.p7	8:123654851	TGCTCAACTAGTGCA[A/T]TGGTCTTCCATGCAT	340359
rs73339443	snp	A/G	0.000399281	0.0141238	intron-variant	KLHL38	GRCh38.p7	8:123646779	TGTCAGATTCTCCAC[A/G]CTCTTCTGGTTGGTT	340359
rs73339449	snp	C/T	0.0023933	0.0345097	intron-variant	KLHL38	GRCh38.p7	8:123648965	ATTTCAAAGCTAGTG[C/T]AAAGTAGATAAGAAA	340359
rs73341470	snp	A/G/T	0.0240737	0.107104	intron-variant	KLHL38	GRCh38.p7	8:123650437	GGTTTAGGGCATCCC[A/G/T]CCTGTGCTCTTAGAG	340359
rs73341473	snp	A/T	0.0310518	0.120672	intron-variant	KLHL38	GRCh38.p7	8:123651177	ATAACAAGTGTTGGT[A/T]TGTGTGTACATGGGT	340359
rs74680308	snp	C/T	0.0429648	0.14013	upstream-variant-2KB	KLHL38	GRCh38.p7	8:123654599	AGGGAGGGAGAGAGA[C/T]GAGAGGAGGAAGAAG	340359
rs74869220	snp	C/T	0.0372196	0.131242	intron-variant	KLHL38	GRCh38.p7	8:123647763	GCATAGTATTCTTTG[C/T]TAGAAAGTCTTTTCC	340359
rs74884256	snp	C/T	0.00322959	0.0400545	missense	KLHL38	GRCh38.p7	8:123652332	TCCAAACCATGAGGG[C/T]CTCAAACACCTTTTC	340359
rs75119354	snp	C/T	0.286564	0.247312	intron-variant	KLHL38	GRCh38.p7	8:123646313	CTTTCTCAGCCTCAT[C/T]GGCCTCTTCCTCTCT	340359
rs75150934	snp	A/T	0.079617	0.182947	upstream-variant-2KB	KLHL38	GRCh38.p7	8:123654557	AGAAGATGAAGGAGG[A/T]TGAGGAGGAAGAAGA	340359
rs75440359	snp	G/T	0.0248432	0.108648	intron-variant	KLHL38	GRCh38.p7	8:123648533	AGAAAAGCAAACACT[G/T]GTTGCATTTTACTTG	340359
rs75443317	snp	A/G	0.0535932	0.154675	intron-variant	KLHL38	GRCh38.p7	8:123647193	AACAGGAAGAAGTAT[A/G]TGATTAAAAATTGAT	340359
rs76305881	snp	A/G	0.0584853	0.160693	intron-variant	KLHL38	GRCh38.p7	8:123646616	AGCAGAAGCAAACAT[A/G]TTTTATTTACCGTGT	340359
rs76493065	snp	A/G	0.5	0	intron-variant	KLHL38	GRCh38.p7	8:123649223	TAGAAAAGAAGGAGG[A/G]GCTCCAGCTTGACAT	340359
rs77162332	snp	A/T	0.0372196	0.131242	intron-variant	KLHL38	GRCh38.p7	8:123647284	CATTGTAATATGGGT[A/T]TTACTTACCTTGCTT	340359
rs77201406	snp	G/T	0.281841	0.247964	intron-variant	KLHL38	GRCh38.p7	8:123646160	ACTAGCACGTGGGAT[G/T]TTGAGCTAACCTGCC	340359
rs77914692	snp	C/T	0.0372196	0.131242	intron-variant	KLHL38	GRCh38.p7	8:123647794	TATAAAATAAAATTA[C/T]GAGGCCGGGTGCGGT	340359
rs78373008	snp	A/G	0.0174175	0.0916809	upstream-variant-2KB	KLHL38	GRCh38.p7	8:123655307	AGGCCAGAATTAGGA[A/G]CAGGAGGCCTAAGCT	340359
rs79116727	snp	A/G	0.00358779	0.0422022	upstream-variant-2KB	KLHL38	GRCh38.p7	8:123654577	GAGGAAGAAGAAGCA[A/G]GGACAGAGGGAGGGA	340359
rs79132421	snp	C/T	0.0146672	0.084371	intron-variant	KLHL38	GRCh38.p7	8:123651407	GCATATATGTGTGCA[C/T]GCATGTATGCATATG	340359
rs79631595	snp	A/G	0.0178098	0.0926698	intron-variant	KLHL38	GRCh38.p7	8:123647696	AAGAGATATAGGATG[A/G]ATTTCATATAAGCAA	340359
rs79974674	snp	C/G	0.0023933	0.0345097	upstream-variant-2KB	KLHL38	GRCh38.p7	8:123654285	TTTGTTGTTGTTGTT[C/G]TTGAGCATCCCAGGG	340359
rs80042966	snp	C/T	0.0240643	0.107019	intron-variant	KLHL38	GRCh38.p7	8:123650171	GGTTTGCTCCAACAT[C/T]CCCTTAACCCTGGCA	340359

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