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
rs2756	snp	C/G	0	0	utr-variant-3-prime	KLHL1	GRCh38.p7	13:69700663	TTTATTAAGGACATT[C/G]TGTAATGTTTCCACT	57626
rs2757	snp	C/T	0	0	utr-variant-3-prime	KLHL1	GRCh38.p7	13:69700689	CCACTTTGTTTTAAA[C/T]AATTACAAACATGTG	57626
rs159918	snp	C/T	0.0150606	0.0854603	intron-variant	KLHL1	GRCh38.p7	13:70101330	CATCTTGTATTTATA[C/T]ATAAGTACATCGTAG	57626
rs159919	snp	A/G	0.0229196	0.104744	intron-variant	KLHL1	GRCh38.p7	13:70071564	tcaccaagacacatc[A/G]cattgcaggccataa	57626
rs299524	snp	A/C	0.363359	0.222822	intron-variant	KLHL1	GRCh38.p7	13:70077056	aagccaccttggaag[A/C]acatttggaagttcc	57626
rs299525	snp	A/C	0.345482	0.231048	intron-variant	KLHL1	GRCh38.p7	13:70078072	TTCTTTTTATTTTTT[A/C]TTTTTTCTGCATTAG	57626
rs299526	snp	A/G	0.153665	0.230694	intron-variant	KLHL1	GRCh38.p7	13:70081228	cagtagaaagttaat[A/G]AGCCAGTGGTACCAG	57626
rs299527	snp	A/C	0.0158469	0.0875917	intron-variant	KLHL1	GRCh38.p7	13:70080980	TGGGAAGAGAAGTCT[A/C]TGAATCAAGCTGGAT	57626
rs299530	snp	C/T	0.488726	0.0742286	intron-variant	KLHL1	GRCh38.p7	13:70070603	tctacctcataagaa[C/T]gttaaagaagttatt	57626
rs299531	snp	G/T	0.488846	0.0738428	intron-variant	KLHL1	GRCh38.p7	13:70070758	AGCTCATGGATAAGC[G/T]AACTAACTGATAATG	57626
rs299532	snp	G/T	0.489083	0.0730708	intron-variant	KLHL1	GRCh38.p7	13:70071466	agaaaatatgtaaaa[G/T]agtggttgaactaaa	57626
rs299533	snp	C/T	0.0185938	0.0946107	intron-variant	KLHL1	GRCh38.p7	13:70095400	ttacatggaatctta[C/T]ttaatgtcattaaga	57626
rs299534	snp	A/G	0.0150606	0.0854603	intron-variant	KLHL1	GRCh38.p7	13:70098956	TGGATTACATGCTTT[A/G]TACTTAGTCAATATT	57626
rs299535	snp	A/G	0.0134861	0.0810011	intron-variant	KLHL1	GRCh38.p7	13:70099683	GAAATACACCATACA[A/G]TAAGCTTTTTGTCCC	57626
rs656920	snp	C/T	0.370568	0.219005	intron-variant	KLHL1	GRCh38.p7	13:70075173	aatccatacatctct[C/T]ccctatgaagagagt	57626
rs659582	snp	A/T	0.407674	0.194008	intron-variant	KLHL1	GRCh38.p7	13:70075788	ACATATATATGTATA[A/T]ATATATGTTGCAGGA	57626
rs662481	snp	A/G	0.382666	0.211895	intron-variant	KLHL1	GRCh38.p7	13:70075691	TATATATACACACAC[A/G]TGTGTATATATGAAA	57626
rs663789	snp	A/G	0.362523	0.223246	intron-variant	KLHL1	GRCh38.p7	13:70075982	actctgaggacaaat[A/G]tcaaagctctaaata	57626
rs683300	snp	C/T	0.370365	0.219117	intron-variant	KLHL1	GRCh38.p7	13:70074705	ACTGAATATGGCTTG[C/T]TGAAAATGCTCTCCA	57626
rs694172	snp	A/C	0.361263	0.223876	intron-variant	KLHL1	GRCh38.p7	13:70074985	AAGCTTTCCCCTGGC[A/C]CCTCCATTATTATAA	57626
rs694227	snp	A/T	0	0	intron-variant	KLHL1	GRCh38.p7	13:70075443	CAAAAAGGTTTTTTT[A/T]AATAAAATTTTGTGG	57626
rs717811	snp	A/G	0.465683	0.126415	intron-variant	KLHL1	GRCh38.p7	13:70031124	gccaaccaaaaaaaa[A/G]cccagatgTTAGCTT	57626
rs717812	snp	A/G	0.34303	0.232046	intron-variant	KLHL1	GRCh38.p7	13:70031447	CAGAGGTTAACAGTT[A/G]CTCAAAATTTACATT	57626
rs868116	snp	C/T	0.492287	0.0616198	intron-variant	KLHL1	GRCh38.p7	13:69938566	TTATCCCTCTGGATA[C/T]GGAGGCATATTTTTC	57626
rs872603	snp	A/T	0.493568	0.0563433	intron-variant	KLHL1	GRCh38.p7	13:69920260	ATTGTCAGTTTCCAA[A/T]TTTTGGAAAACAGTA	57626
rs872604	snp	A/G	0.0425829	0.139564	intron-variant	KLHL1	GRCh38.p7	13:69920479	GCAAAGTTACTTAAC[A/G]CATATCAGAAAAGGG	57626
rs928022	snp	A/C	0.159951	0.233219	intron-variant	KLHL1	GRCh38.p7	13:70094590	GAAGAGCACAGAATT[A/C]ATCTGTAAACCACCA	57626
rs928023	snp	A/G	0.158962	0.232835	intron-variant	KLHL1	GRCh38.p7	13:70094711	TTTGTGGCAATTTCA[A/G]TGTGGCTTCCTTAGC	57626
rs962827	snp	A/C	0.26271	0.249677	intron-variant	KLHL1	GRCh38.p7	13:70028314	TTTGCGGCCCATGGA[A/C]AGCCAAAAATATGAA	57626
rs962828	snp	C/G	0.26271	0.249677	intron-variant	KLHL1	GRCh38.p7	13:70028358	CAGTATATATATAGA[C/G]AGAGGTATGTCTTGA	57626
rs962829	snp	C/T	0.262985	0.249663	intron-variant	KLHL1	GRCh38.p7	13:70028716	GCATGGTAGTTTATG[C/T]CTGTAATCCCAGCAG	57626
rs962830	snp	C/T	0.262159	0.249704	intron-variant	KLHL1	GRCh38.p7	13:70028773	CTTGAGCCCAGGAGA[C/T]TGAGACCAACCTTCG	57626
rs962831	snp	C/T	0.262435	0.249691	intron-variant	KLHL1	GRCh38.p7	13:70028809	TGGCGAAACTTCATC[C/T]CTACAGAAAATACAA	57626
rs973540	snp	A/G	0.435694	0.167385	intron-variant	KLHL1	GRCh38.p7	13:69861066	CATCAGTAAAATAAA[A/G]TATGTTTTTAATAGC	57626
rs975701	snp	A/C	0.456214	0.141336	intron-variant	KLHL1	GRCh38.p7	13:69758099	ctcagattttttgat[A/C]gtttgatggtttgaa	57626
rs978025	snp	A/G	0.290201	0.246747	intron-variant	KLHL1	GRCh38.p7	13:70025253	TTAAATATAATCTAC[A/G]AGTATAATGTGCTGA	57626
rs978026	snp	C/T	0.29046	0.246704	intron-variant	KLHL1	GRCh38.p7	13:70025307	CCAAAACATAGGCTG[C/T]AATTCTCAGTGGTGA	57626
rs978027	snp	C/T	0.289942	0.246789	intron-variant	KLHL1	GRCh38.p7	13:70025345	TAGTTGACTTTGAGG[C/T]GGAATTATTTTATGC	57626
rs978028	snp	C/T	0.29046	0.246704	intron-variant	KLHL1	GRCh38.p7	13:70025611	CTAAGAAAAAGTAAA[C/T]TAGGAGATGCTATCT	57626
rs978029	snp	A/T	0.290718	0.246662	intron-variant	KLHL1	GRCh38.p7	13:70025692	TTTTACTATATATAT[A/T]ATATATAGTATACAT	57626
rs978885	snp	C/T	0.440471	0.161928	intron-variant	KLHL1	GRCh38.p7	13:70053741	ACCTCTACATAAAAT[C/T]ACTGAATAAAATGAC	57626
rs978886	snp	A/G	0	0	intron-variant	KLHL1	GRCh38.p7	13:70053980	ATCCTGAATGTGACA[A/G]GTTTTGTGTGGCCTT	57626
rs980122	snp	A/C	0.365853	0.221536	intron-variant	KLHL1	GRCh38.p7	13:70087691	TGGTTGTTTTTCTCC[A/C]TCATTTTAAATCCCA	57626
rs980123	snp	A/G	0.315516	0.241263	intron-variant	KLHL1	GRCh38.p7	13:70087594	GCATTGGGTTTGGTC[A/G]TTGGATTTGCAATGT	57626
rs981349	snp	C/T	0.251578	0.249995	intron-variant	KLHL1	GRCh38.p7	13:70024298	CTTAATTCAAAGAAA[C/T]CTAGTAGTTTATATT	57626
rs981350	snp	C/G	0.256619	0.249912	intron-variant	KLHL1	GRCh38.p7	13:70024319	AGTTTATATTTTCAT[C/G]ATAACCATAACACTT	57626
rs981351	snp	A/G	0.255782	0.249933	intron-variant	KLHL1	GRCh38.p7	13:70024413	GAAAAAACTCAGGGG[A/G]CTTGCCATGAGTGTT	57626
rs981538	snp	A/G	0.0154538	0.0865337	intron-variant	KLHL1	GRCh38.p7	13:69760853	AAATTACAGTGGGAC[A/G]TTCAAAATAAACTAT	57626
rs990612	snp	C/G	0.486133	0.082104	intron-variant	KLHL1	GRCh38.p7	13:69718390	CTTTTGACATAGAGA[C/G]CAGCAATGATCAATA	57626
rs990613	snp	C/T	0.116838	0.211584	intron-variant	KLHL1	GRCh38.p7	13:69718594	CATTTCCCCATGGAT[C/T]ATTATGTATCCTATG	57626
rs990614	snp	A/T	0.189245	0.244197	intron-variant	KLHL1	GRCh38.p7	13:69718735	CAGAAGTCTCTGCAT[A/T]GTATTCCTAGGCCTG	57626
rs990615	snp	A/C	0.486133	0.082104	intron-variant	KLHL1	GRCh38.p7	13:69718394	TGACATAGAGACCAG[A/C]AATGATCAATATTCT	57626
rs993138	snp	G/T	0.465368	0.126951	intron-variant	KLHL1	GRCh38.p7	13:69805021	AAACTTTATTTTTCA[G/T]AGAAATATGAATACA	57626
rs993139	snp	C/T	0.465158	0.127307	intron-variant	KLHL1	GRCh38.p7	13:69804984	TCAATGAAATGCTTA[C/T]ACTATAAAACATTGA	57626
rs993140	snp	A/G	0.498547	0.0269177	intron-variant	KLHL1	GRCh38.p7	13:69804869	ACTATTCCAAAATGC[A/G]TCTCACTATTTCCTG	57626
rs993141	snp	A/G	0.405776	0.195535	intron-variant	KLHL1	GRCh38.p7	13:69804846	ATTTCCTGCTTTTTA[A/G]AAGACAATACATCAA	57626
rs993907	snp	A/T	0.31721	0.240796	intron-variant	KLHL1	GRCh38.p7	13:70093909	ATAAAGTTAATTAAC[A/T]TGTTTGAATAATTAA	57626
rs1019580	snp	C/T	0.0535932	0.154675	intron-variant	KLHL1	GRCh38.p7	13:69854723	TTACTAACAATTTTG[C/T]TCCAGTTTCTAGAAC	57626
rs1019581	snp	C/T	0.084728	0.187577	intron-variant	KLHL1	GRCh38.p7	13:69854915	TACCTATTTTTGAAA[C/T]GGTGCCAACTGGAAA	57626
rs1025821	snp	C/T	0.316968	0.240864	intron-variant	KLHL1	GRCh38.p7	13:70050131	AAAAAACAAACAGCC[C/T]CTAATTTTATAATAT	57626
rs1030272	snp	A/G			intron-variant	KLHL1	GRCh38.p7	13:69780757	tataaatgtgtgtgt[A/G]tatatatatatgtat	57626
rs1030274	snp	C/G	0.441295	0.160954	intron-variant	KLHL1	GRCh38.p7	13:69779935	gtgccagtaatactt[C/G]ggaggctgtggccgg	57626
rs1030275	snp	A/G	0.334412	0.235318	intron-variant	KLHL1	GRCh38.p7	13:69779879	aggttgcagtgagcc[A/G]agatcgcaccattgc	57626
rs1030276	snp	A/G	0.383053	0.211653	intron-variant	KLHL1	GRCh38.p7	13:69779649	GATAAAGATATAGAC[A/G]TATGTGTTTACAATT	57626
rs1030277	snp	A/T	0.381113	0.21286	intron-variant	KLHL1	GRCh38.p7	13:69756242	CATAAATTATCAATA[A/T]CTGCCACAGAGTTAT	57626
rs1118693	snp	A/G	0.173643	0.238054	intron-variant	KLHL1	GRCh38.p7	13:69722946	atggagcacatttcc[A/G]ttatccatttatcca	57626
rs1118694	snp	C/T	0.440195	0.162252	intron-variant	KLHL1	GRCh38.p7	13:69722846	gctgtttctcttata[C/T]actggtttcatttcc	57626
rs1118695	snp	C/T	0.187053	0.241946	intron-variant	KLHL1	GRCh38.p7	13:69722820	tttcctttgaatata[C/T]accaagtagtgagat	57626
rs1119836	snp	A/G	0.0244538	0.107838	intron-variant	KLHL1	GRCh38.p7	13:69763144	gtctgttgtgcaacc[A/G]tggcctttgcagtag	57626
rs1273101	snp	A/T	0	0	intron-variant	KLHL1	GRCh38.p7	13:69787021	ggaatgttcttccat[A/T]tgtttgtatcctctt	57626
rs1318761	snp	A/G	0.395818	0.203069	intron-variant	KLHL1	GRCh38.p7	13:69790192	GTTGTTATTCATGCA[A/G]TTCCTGACAATGTCA	57626
rs1328604	snp	C/T	0.35445	0.227135	intron-variant	KLHL1	GRCh38.p7	13:70103151	CATCTCTGTGATGAA[C/T]AGGGATGAACTCAGG	57626
rs1328622	snp	A/C	0.270351	0.24917	intron-variant	KLHL1	GRCh38.p7	13:70083723	TGTAATTATATACGA[A/C]TTAATATTTACAATA	57626
rs1328623	snp	C/T	0.289424	0.246872	intron-variant	KLHL1	GRCh38.p7	13:70092551	TTTTATATTATTAGA[C/T]ACAAAGTTTAATTAA	57626
rs1330084	snp	A/G	0.193966	0.243639	intron-variant	KLHL1	GRCh38.p7	13:69718659	TCTTCAGTCCTTACT[A/G]CATACCATATAATAG	57626
rs1330085	snp	A/G	0.45762	0.139261	intron-variant	KLHL1	GRCh38.p7	13:69718668	CTTACTACATACCAT[A/G]TAATAGTTCTAAGTA	57626
rs1330093	snp	C/T	0.441295	0.160954	downstream-variant-500B	KLHL1	GRCh38.p7	13:69700441	AACAATAATTAAAAT[C/T]ACATTTGGTGTCAGC	57626
rs1345908	snp	A/G			intron-variant	KLHL1	GRCh38.p7	13:69718230	AGTATCCCAACTTGT[A/G]TCTGGGAGAAAAGCG	57626
rs1345909	snp	G/T			intron-variant	KLHL1	GRCh38.p7	13:69712783	TTTTTGGGGGGGGGG[G/T]TTTGTTTGTTTGCTT	57626
rs1348175	snp	C/T	0.0119091	0.0762411	intron-variant	KLHL1	GRCh38.p7	13:70061732	CCAGGTTCTTGCATT[C/T]TCAAATTCCTTGCTA	57626
rs1348176	snp	C/T	0.426507	0.177046	intron-variant	KLHL1	GRCh38.p7	13:70062174	GCACGCTTGTATTTT[C/T]TGAAACATAACAAAT	57626
rs1360011	snp	C/T	0.319136	0.24025	intron-variant	KLHL1	GRCh38.p7	13:70083264	AAGGCATAATAATGA[C/T]GTAGGAGTAAAATAA	57626
rs1364376	snp	C/T	0.0748431	0.178382	intron-variant	KLHL1	GRCh38.p7	13:69767312	TATAACAAACTTAGG[C/T]TTTTCCTAATGATCC	57626
rs1364377	snp	A/G	0.461037	0.134028	intron-variant	KLHL1	GRCh38.p7	13:69755494	ATATTTTAATACCAT[A/G]TGTTTACAAATTGTG	57626
rs1364378	snp	A/T	0.0894459	0.191631	intron-variant	KLHL1	GRCh38.p7	13:69854203	AAAGAAAAGAGGTTT[A/T]TTTGGCTCATAGTTC	57626
rs1364379	snp	C/T	0.320096	0.239972	intron-variant	KLHL1	GRCh38.p7	13:69854338	TCACGCAGCAAGAAA[C/T]GAAGAAAGAGAGAGA	57626
rs1364380	snp	A/G	0.469049	0.120489	intron-variant	KLHL1	GRCh38.p7	13:69854536	CCAAACCACAGCACA[A/G]GCACATAAGAAAGGC	57626
rs1372230	snp	A/T	0.273049	0.248935	intron-variant	KLHL1	GRCh38.p7	13:70027358	CCATAGGAGCGTAAA[A/T]CCCTTTAGAGCCAGT	57626
rs1372231	snp	G/T	0.294064	0.246086	intron-variant	KLHL1	GRCh38.p7	13:70027546	AAAGGGGGAGAAAAC[G/T]ATAACAAAAGTTGAT	57626
rs1372232	snp	A/T	0.0333695	0.124785	intron-variant	KLHL1	GRCh38.p7	13:70065635	CAGAAAATTTTAGGG[A/T]ACAAAAGATTTCCCT	57626
rs1372281	snp	A/G	0.0142736	0.0832652	intron-variant	KLHL1	GRCh38.p7	13:70016445	agggagctagagcag[A/G]cacttacgagcctac	57626
rs1372282	snp	C/T	0.499295	0.0187567	intron-variant	KLHL1	GRCh38.p7	13:70014617	GAGATTTTCATTATA[C/T]ATGCATGGATGATAA	57626
rs1372283	snp	C/G	0.393987	0.204372	intron-variant	KLHL1	GRCh38.p7	13:70065725	GTAAATCTGTCCAAA[C/G]CAGAACATTTGCAGT	57626
rs1372284	snp	A/G	0.109814	0.206997	intron-variant	KLHL1	GRCh38.p7	13:70065808	TTTATGTAAAGGCTT[A/G]GCAGGTGGATTAGCA	57626
rs1372285	snp	A/C	0.093417	0.194889	intron-variant	KLHL1	GRCh38.p7	13:70067360	TATTCTTATTCCATT[A/C]TTATTTTATATTGAT	57626
rs1372286	snp	C/T	0.404384	0.196635	intron-variant	KLHL1	GRCh38.p7	13:70067425	AAGGGGAAAGAATTG[C/T]CAAATGTCACACAGC	57626
rs1372287	snp	C/G	0.41275	0.189769	intron-variant	KLHL1	GRCh38.p7	13:70067616	GGTCTTAGTACAGGG[C/G]CTCAGATGACATATT	57626
rs1411333	snp	C/T	0.0364509	0.129988	intron-variant	KLHL1	GRCh38.p7	13:69709210	AACATCACAGATAGA[C/T]GCAGACATACATAGA	57626
rs1424300	snp	C/T	0.000399281	0.0141238	intron-variant	KLHL1	GRCh38.p7	13:69759468	attggtaaaataaaa[C/T]agaaatgtctccaaa	57626
rs1424301	snp	A/G	0.357024	0.225933	intron-variant	KLHL1	GRCh38.p7	13:69741581	TCTTTGGATCACCCT[A/G]TGGGAATTGGGGCGT	57626

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