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
rs725716	snp	A/T	0.121838	0.21465	intron-variant	KLHL13	GRCh38.p7	X:117970416	TATTGAGGAGTCAGA[A/T]TTGAACAATTCTATT	90293
rs765236	snp	A/G	0.11443	0.21005	intron-variant	KLHL13	GRCh38.p7	X:117989472	TTTTTTTTTTGGAGG[A/G]GAGGTGTTTAGGAGT	90293
rs877902	snp	A/T	0.00528398	0.051128	intron-variant	KLHL13	GRCh38.p7	X:117922856	TTACTAGAAGTAACC[A/T]CTGTTAACAGTTTAG	90293
rs879370	snp	C/T	0.0292288	0.117303	intron-variant	KLHL13	GRCh38.p7	X:117923522	TTGTTTGTTTTTGTT[C/T]TTTAGTGGAAGAAAA	90293
rs1985828	snp	G/T			intron-variant	KLHL13	GRCh38.p7	X:118106085	ttttttttttttttg[G/T]atttttagtagaaca	90293
rs2041633	snp	C/T	0.122299	0.214924	intron-variant	KLHL13	GRCh38.p7	X:117909159	GCATAAAGATGGTCT[C/T]CAATATTTTCTCAGA	90293
rs2041641	snp	C/T	0.0600656	0.162557	intron-variant	KLHL13	GRCh38.p7	X:117947130	TATATTTATGATATA[C/T]AGCACACACACACAA	90293
rs2080139	snp	C/T	0.0194105	0.0965841	intron-variant	KLHL13	GRCh38.p7	X:118027132	gccaaaggactatat[C/T]atctgtttattatga	90293
rs2106680	snp	A/T	0.224335	0.248679	intron-variant	KLHL13	GRCh38.p7	X:118103240	AATATAAAGGTATGC[A/T]TAGATTTTTTATTCT	90293
rs2106681	snp	A/C	0.0860103	0.188699	intron-variant	KLHL13	GRCh38.p7	X:118103242	TATAAAGGTATGCAT[A/C]GATTTTTTATTCTAG	90293
rs2106682	snp	C/T	0.0860103	0.188699	intron-variant	KLHL13	GRCh38.p7	X:118103294	TGATTTTATCCTACC[C/T]ACTAGCTGTGAGATC	90293
rs2106683	snp	C/T	0.223547	0.248597	intron-variant	KLHL13	GRCh38.p7	X:118103312	TAGCTGTGAGATCAC[C/T]ACACCTTTTGCCATA	90293
rs2110256	snp	A/G			intron-variant	KLHL13	GRCh38.p7	X:118008086	AAGCATCCACATTAA[A/G]GCTCTGAATTATTTC	90293
rs2110257	snp	A/G			intron-variant	KLHL13	GRCh38.p7	X:118008162	CACAACTGTTGTTCA[A/G]GAGCCTTTGAAAATT	90293
rs2158018	snp	A/G	0.00633741	0.0559334	intron-variant	KLHL13	GRCh38.p7	X:118105941	gagtctcgctctgtc[A/G]cccaggctggagtgc	90293
rs2188745	snp	A/G	0.0590711	0.161388	intron-variant	KLHL13	GRCh38.p7	X:118081441	CCATTTGTTACAGTG[A/G]TGTTGATTTTTGGTT	90293
rs2192259	snp	A/G	0.11768	0.212112	intron-variant	KLHL13	GRCh38.p7	X:118012846	cagcctctaaagaag[A/G]tatatatacaaacaa	90293
rs2192260	snp	A/G	0.118143	0.2124	intron-variant	KLHL13	GRCh38.p7	X:118016501	CATCCAGTAATTGTT[A/G]ATAAATGGTACAACT	90293
rs2192261	snp	C/T	0.118143	0.2124	intron-variant	KLHL13	GRCh38.p7	X:118016556	ACTATGTGCAAAATC[C/T]TGCATTATGTACAAT	90293
rs2428310	snp	C/T	0.370254	0.219178	intron-variant	KLHL13	GRCh38.p7	X:118079954	accaatggaacagaa[C/T]agaaaactcagaaat	90293
rs2428311	snp	C/T	0.384163	0.210951	intron-variant	KLHL13	GRCh38.p7	X:118080025	aacaaatacaagcaa[C/T]gggataaggactccc	90293
rs2428312	snp	C/T	0.0797195	0.183042	intron-variant	KLHL13	GRCh38.p7	X:118093690	TCTAAATTAATTTTG[C/T]AACTTATTAGTACAT	90293
rs2428313	snp	C/T	0.123219	0.215468	intron-variant	KLHL13	GRCh38.p7	X:118069758	tacagtaagttaagg[C/T]taatttattaccaaa	90293
rs2428314	snp	C/T	0.0797195	0.183042	intron-variant	KLHL13	GRCh38.p7	X:118100177	AACATTTTCACTTTC[C/T]ACAAAACAATTTTTG	90293
rs2430207	snp	C/T	0.373206	0.217533	intron-variant	KLHL13	GRCh38.p7	X:117960368	TTAGAAATGCCACTT[C/T]TGAGGCCATAACTTG	90293
rs2430208	snp	A/G	0.0465453	0.14528	upstream-variant-2KB, intron-variant	KLHL13	GRCh38.p7	X:117985965	CTTTTTAAAAATAAA[A/G]CTACACATGATGTAA	90293
rs2430209	snp	A/G	0.353269	0.227674	intron-variant	KLHL13	GRCh38.p7	X:117994885	acatagtgagacttc[A/G]tctgtataaaaaata	90293
rs2430210	snp	A/C	0.0590711	0.161388	intron-variant	KLHL13	GRCh38.p7	X:118000335	GTCCTAAAATTGCTA[A/C]AAGATAAACTTAATT	90293
rs2430211	snp	A/C	0.0595685	0.161975	intron-variant	KLHL13	GRCh38.p7	X:118014260	ttaataattgggacc[A/C]tggggaagaaatgca	90293
rs2430212	snp	C/T	0.499262	0.0191911	intron-variant	KLHL13	GRCh38.p7	X:117954093	GCTAGACAAATGATA[C/T]TCCATTAGATAACTA	90293
rs2430213	snp	G/T	0.0209675	0.10022	intron-variant	KLHL13	GRCh38.p7	X:117954251	TTCATCTTTTAAAAT[G/T]TATATACCAGTTAAA	90293
rs2430214	snp	C/G	0.0600656	0.162557	intron-variant, utr-variant-5-prime	KLHL13	GRCh38.p7	X:118029149	GAATAAACTGAGAAT[C/G]AGAAGACCTAAGGAC	90293
rs2430215	snp	G/T	0.499283	0.0189268	intron-variant	KLHL13	GRCh38.p7	X:118032227	ggaagcttgaactgg[G/T]tggagcccaccacag	90293
rs2465938	snp	A/G	0.0595685	0.161975	intron-variant	KLHL13	GRCh38.p7	X:118008851	atcattattattccc[A/G]ttttacaaacaagga	90293
rs2465939	snp	A/G	0.0470497	0.145984	intron-variant	KLHL13	GRCh38.p7	X:118007227	agatggggtctcgct[A/G]tgttcaccaggctgg	90293
rs2465940	snp	A/G	0.0209675	0.10022	intron-variant	KLHL13	GRCh38.p7	X:118006509	AGGAAAAGATTGTAG[A/G]GATAGTGTTAACCCT	90293
rs2465941	snp	C/T	0.0585734	0.160798	intron-variant	KLHL13	GRCh38.p7	X:118003968	TTGTTTGCATTTCAC[C/T]GTACCACATCAGTCC	90293
rs2497841	snp	G/T			intron-variant	KLHL13	GRCh38.p7	X:117978018	CTTACTAGATACTCA[G/T]ATATGTAGTCTTGCC	90293
rs2497842	snp	C/T	0.0590711	0.161388	intron-variant	KLHL13	GRCh38.p7	X:118003407	TTATATTTATCACTG[C/T]TGTTTGTTTAGTTAG	90293
rs2497843	snp	C/T	0.0460406	0.14457	intron-variant	KLHL13	GRCh38.p7	X:118014484	acaatgcatgcacag[C/T]ggcacacagaccctc	90293
rs2497844	snp	A/T	0.0590711	0.161388	intron-variant	KLHL13	GRCh38.p7	X:118017673	TCCTTTCAACAGCAC[A/T]TAAGAAACACAATTA	90293
rs2497845	snp	C/G	0.372671	0.217834	intron-variant	KLHL13	GRCh38.p7	X:118027431	ttaaattcccaggac[C/G]ctcagttctttaaat	90293
rs2497846	snp	A/G/T	0.422378	0.183357	intron-variant	KLHL13	GRCh38.p7	X:118032211	gtaaacaaagcagcc[A/G/T]ggaagcttgaactgg	90293
rs2497847	snp	A/G	0.0455357	0.143855	intron-variant	KLHL13	GRCh38.p7	X:118080974	agcaacatagatgca[A/G]ctagacgccataatc	90293
rs2497848	snp	G/T	0.381341	0.212719	intron-variant	KLHL13	GRCh38.p7	X:118081453	GTGATGTTGATTTTT[G/T]Gttttttttaactga	90293
rs2497849	snp	A/G	0.0797195	0.183042	intron-variant	KLHL13	GRCh38.p7	X:118085158	gataaatgaataaac[A/G]taagtagtagtatat	90293
rs2497850	snp	A/G	0.498408	0.028167	intron-variant	KLHL13	GRCh38.p7	X:118102100	GTGAGAGAGGTGCTA[A/G]AGGGACAGGCAGGAG	90293
rs2497851	snp	A/G	0.3777	0.214925	intron-variant	KLHL13	GRCh38.p7	X:118104197	actgcattctagcct[A/G]gaaaacagaatgaaa	90293
rs2497852	snp	A/G	0.383908	0.211113	intron-variant	KLHL13	GRCh38.p7	X:118105426	ttatccagcatctat[A/G]tgcctcagtttcctc	90293
rs2497853	snp	A/G	0.0792336	0.182589	intron-variant	KLHL13	GRCh38.p7	X:118107592	cttagcactctatac[A/G]cattattaatttaat	90293
rs2497854	snp	G/T	0.120916	0.214097	intron-variant	KLHL13	GRCh38.p7	X:118110474	ACCTCCAACTCCCTG[G/T]CTCAAGCGATTCTCC	90293
rs2497855	snp	A/G	0.0450304	0.143134	intron-variant	KLHL13	GRCh38.p7	X:118116180	CCCCAGACCGTCAGG[A/G]CAGCAACAGCGAGGC	90293
rs2497856	snp	A/G	0.0450304	0.143134	intron-variant	KLHL13	GRCh38.p7	X:118116347	CACCAGCACGCGGGA[A/G]AAAAAGAGGGGGCGG	90293
rs2497857	snp	A/G	0.0445249	0.142408	upstream-variant-2KB	KLHL13	GRCh38.p7	X:118117909	ACCAGTTTAATCACT[A/G]TTGTGATTTTTTTTC	90293
rs2497858	snp	A/C	0.390203	0.206986	intron-variant	KLHL13	GRCh38.p7	X:117957478	TTACTTACAAACTAC[A/C]AATTGTTTTGCTTTG	90293
rs2497859	snp	G/T	0.0605624	0.163136	intron-variant	KLHL13	GRCh38.p7	X:117959035	ATCTGCAATTTTAAT[G/T]ATATGGAAGAAAGTC	90293
rs2497860	snp	A/C	0.0147244	0.0845304	intron-variant, utr-variant-5-prime	KLHL13	GRCh38.p7	X:117973462	CTGTGCAAGCTCTGG[A/C]CACACAAATCAAGAA	90293
rs2497861	snp	C/T	0.0580755	0.160203	intron-variant, upstream-variant-2KB	KLHL13	GRCh38.p7	X:117975207	acacacacacagcca[C/T]acacaTGTATGAACA	90293
rs2516003	snp	A/T	0.0450304	0.143134	intron-variant	KLHL13	GRCh38.p7	X:117967746	TATTGTGTATTTTTT[A/T]AAAAGACCTCTTGAA	90293
rs2516004	snp	C/G	0.373739	0.21723	upstream-variant-2KB, intron-variant	KLHL13	GRCh38.p7	X:117986318	AATTTGCTGATCCCT[C/G]CAACATGTTGTATTC	90293
rs3046168	in-del	-/GAAAGAAA/GAAAGAAAGAAA/GAAAGAAAGAAAGAAA/GAAAGAAT			intron-variant	KLHL13	GRCh38.p7	X:118089669	AAAGAAAGAAAGAAA[lengthTooLong]AAAGAAAGTTTCAAT	90293
rs3071303	in-del	-/ATTTT			intron-variant	KLHL13	GRCh38.p7	X:117979811	TTTATTGGAATATTT[-/ATTTT]ATTTAAGAAAGTATA	90293
rs3071305	in-del	-/GT			intron-variant	KLHL13	GRCh38.p7	X:117948133	agagaactgtcctgt[-/GT]tttgtaggatgttta	90293
rs3886411	snp	C/T	0.373206	0.217533	intron-variant	KLHL13	GRCh38.p7	X:118046904	TCACCACTCATATTA[C/T]AATTGTTAAATCAAG	90293
rs4025518	in-del	-/GT			intron-variant	KLHL13	GRCh38.p7	X:118085842	TGTGTGTGTGTGTGT[-/GT]ATCATATATTCTTCA	90293
rs4262469	snp	G/T	0.374005	0.217078	intron-variant	KLHL13	GRCh38.p7	X:118063754	TCAAATTCCTCTATT[G/T]CAAAAAGGTCATTGT	90293
rs4281266	snp	G/T	0.419682	0.183598	intron-variant	KLHL13	GRCh38.p7	X:118044246	ggacacaacaaaatg[G/T]aaagatatttcatct	90293
rs4623627	snp	A/C	0.375	0.216506	intron-variant	KLHL13	GRCh38.p7	X:117930290	AGGAAGGAAGGAAGG[A/C]AGGCAGGCAGGCAGG	90293
rs4825549	snp	C/G	0.428553	0.174982	intron-variant	KLHL13	GRCh38.p7	X:117943050	tctcagcattttctt[C/G]tctgtaaaggatttt	90293
rs4825555	snp	C/T	0.372671	0.217834	intron-variant	KLHL13	GRCh38.p7	X:118051465	agaatggcatgaacc[C/T]gggaggcagagcttg	90293
rs4825556	snp	A/T	0.0575773	0.159604	intron-variant	KLHL13	GRCh38.p7	X:118051743	AAATTCAATACAATT[A/T]CAATCAAATTCCCTA	90293
rs4825557	snp	A/G	0.322218	0.239342	intron-variant	KLHL13	GRCh38.p7	X:118106549	TAATATATTTCATCA[A/G]TATAGTGAGCTAAGC	90293
rs5011167	snp	A/G	0.349514	0.22934	intron-variant	KLHL13	GRCh38.p7	X:117930242	aggaaggaaggaagg[A/G]aggaaggaaggaagg	90293
rs5011168	snp	A/G	0.0131573	0.0800346	intron-variant	KLHL13	GRCh38.p7	X:117930246	aggaaggaagggagg[A/G]aggaaggaaggaagg	90293
rs5903508	in-del	-/A			intron-variant	KLHL13	GRCh38.p7	X:117996845	AAAAAAAAAAAAAAA[-/A]GCTACATGTGCTATG	90293
rs5903510	in-del	-/T	0.0860103	0.188699	intron-variant	KLHL13	GRCh38.p7	X:118103857	AAGTCAGTGGCCGAA[-/T]TTTTTTTAATTCCAG	90293
rs5910266	snp	A/T	0.022522	0.1037	intron-variant	KLHL13	GRCh38.p7	X:117911356	AGTTAGGATATAATA[A/T]CACTGAAATCTCTAA	90293
rs5910274	snp	A/T	0.022522	0.1037	intron-variant	KLHL13	GRCh38.p7	X:117930528	gaaattcaaattaTG[A/T]ATTCCAGCATAGTTG	90293
rs5910289	snp	G/T	0.00211696	0.0324653	intron-variant	KLHL13	GRCh38.p7	X:118083548	tctcatagaagtaga[G/T]agtagaatagtggtt	90293
rs5910291	snp	C/T	0.320952	0.23972	intron-variant	KLHL13	GRCh38.p7	X:118092908	GCAAGTTCATGTGAA[C/T]CTGTAATTATTTCAA	90293
rs5910292	snp	C/T	0.00105904	0.0229869	intron-variant	KLHL13	GRCh38.p7	X:118113937	TAGTAAATGAATGAA[C/T]GATACATAAAAACCT	90293
rs5955986	snp	A/C/G	0.00211696	0.0324653	intron-variant	KLHL13	GRCh38.p7	X:117908402	tcccctagcccccca[A/C/G]ccccagacaggccct	90293
rs5955987	snp	C/T	0.272746	0.248963	intron-variant	KLHL13	GRCh38.p7	X:117913950	GCTCATTTACATTTC[C/T]TTGatataaattatt	90293
rs5955988	snp	C/T	0.121838	0.21465	intron-variant	KLHL13	GRCh38.p7	X:117913996	ataaCCAAACAACAG[C/T]CATAGTCATCCTAAA	90293
rs5955989	snp	C/G	0.374005	0.217078	intron-variant	KLHL13	GRCh38.p7	X:117914268	gccgagtgaagcagt[C/G]aaagtgaagaaggaa	90293
rs5955990	snp	C/T	0.272746	0.248963	intron-variant	KLHL13	GRCh38.p7	X:117916514	GGTTGGCTCTTGTTC[C/T]ATTAACACTGATGCT	90293
rs5955993	snp	C/G	0.353869	0.227401	intron-variant	KLHL13	GRCh38.p7	X:117970106	AAGAGACCATGGAGC[C/G]TTTAGATTTTTCCCA	90293
rs5955994	snp	C/T	0.114895	0.210349	intron-variant	KLHL13	GRCh38.p7	X:117992165	TTGGATGGGGTTCTG[C/T]TTCAAGGAAGTTAGC	90293
rs5955995	snp	C/T	0.114895	0.210349	intron-variant	KLHL13	GRCh38.p7	X:117992972	ACTAAGTAAACCCAG[C/T]TTCTCACCTTCAAGG	90293
rs5955996	snp	C/G	0.0379276	0.132383	intron-variant	KLHL13	GRCh38.p7	X:118004470	tggaatgtaatgaag[C/G]actcagaaagtacaa	90293
rs5955998	snp	A/C	0.114895	0.210349	intron-variant	KLHL13	GRCh38.p7	X:118014672	gacgatatgtgactt[A/C]gcctccagcggccca	90293
rs5955999	snp	A/G	0.114895	0.210349	intron-variant	KLHL13	GRCh38.p7	X:118014957	CAGACATGATATATA[A/G]TATAATAAAACAGTA	90293
rs5956000	snp	C/T	0.114895	0.210349	intron-variant	KLHL13	GRCh38.p7	X:118015119	GAGTTAAGACACTTT[C/T]CAAATTTCACACAGC	90293
rs5956001	snp	C/T	0.121377	0.214374	intron-variant	KLHL13	GRCh38.p7	X:118032414	cgggcagactgcctc[C/T]tcaagtgggtccctg	90293
rs5956003	snp	C/T	0.0348667	0.127349	intron-variant	KLHL13	GRCh38.p7	X:118045623	agctggccaacatga[C/T]gaaaatccatgtcta	90293
rs5956004	snp	G/T	0.114895	0.210349	intron-variant	KLHL13	GRCh38.p7	X:118045782	actgcactccagctt[G/T]ggcagcagagtgaga	90293
rs5956005	snp	A/G	0.0068637	0.0581785	intron-variant	KLHL13	GRCh38.p7	X:118066590	tttaggttaggcaaa[A/G]atcttgtagctatga	90293
rs5956007	snp	A/T	0.373739	0.21723	intron-variant	KLHL13	GRCh38.p7	X:118090322	caaaagaaactacca[A/T]aagagtgaacaggca	90293
rs5956008	snp	A/C	0.373739	0.21723	intron-variant	KLHL13	GRCh38.p7	X:118090323	aaaagaaactaccaa[A/C]agagtgaacaggcaa	90293
rs5956009	snp	A/C	0.327237	0.23777	intron-variant	KLHL13	GRCh38.p7	X:118092985	TTCCTAATAGTGAAA[A/C]AATTTTAAAACAAAT	90293

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