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
rs9261	snp	C/T	0.497776	0.0332724	utr-variant-3-prime, intron-variant	KLHL29, ATAD2B	GRCh38.p7	2:23708166	AAATTCCAGTTCTAA[C/T]GTTGGGCATCAACTT	114818
rs472798	snp	C/T	0.0755793	0.179102	intron-variant	KLHL29	GRCh38.p7	2:23601749	CTGAGGTTGGTAGGT[C/T]CCCAGGCTAGCCCAC	114818
rs473553	snp	C/T	0.305934	0.243663	intron-variant	KLHL29	GRCh38.p7	2:23627298	GAACCAAGGTGGGGC[C/T]AAAGAACACCACGCC	114818
rs473796	snp	A/C	0.157972	0.232445	intron-variant, nc-transcript-variant	KLHL29, LOC102723401	GRCh38.p7	2:23617904	GGGCCGCGAGAGGGA[A/C]CCGAGGGTGTTGGAA	114818
rs475309	snp	A/G	0.158962	0.232835	intron-variant	KLHL29	GRCh38.p7	2:23627443	TGGAACATTCCCACC[A/G]CGGAGCGGTCATTTC	114818
rs477284	snp	A/G	0.255503	0.249939	intron-variant	KLHL29	GRCh38.p7	2:23627705	GTGTCTAATAAGGTC[A/G]CTGAGGATGTCGTGT	114818
rs482525	snp	A/G	0.21303	0.247251	intron-variant	KLHL29	GRCh38.p7	2:23637670	TCTGCACTATGCGTC[A/G]AAGCCCCAAGTGTTG	114818
rs482639	snp	A/C	0.49607	0.0441545	intron-variant	KLHL29	GRCh38.p7	2:23637704	AGCCTCCGCATCCAC[A/C]CCCCCTTTCTGTCCC	114818
rs485251	snp	A/G	0.195526	0.243993	intron-variant	KLHL29	GRCh38.p7	2:23631392	GTAATTTAGCAGCAA[A/G]TTGATAGAGAAAGGT	114818
rs487305	snp	C/T	0.266	0.249487	intron-variant	KLHL29	GRCh38.p7	2:23615617	CTGGGCGGAGGGAAG[C/T]TGCTGAAGTTGCACT	114818
rs488971	snp	C/T	0.337614	0.234145	intron-variant	KLHL29	GRCh38.p7	2:23631766	TTTGGTGGCTCTCAA[C/T]GTGTCCTTCTGACCC	114818
rs491421	snp	C/T	0.495708	0.0461266	intron-variant, upstream-variant-2KB	KLHL29	GRCh38.p7	2:23641430	TGCGAGGACCATGCC[C/T]GGCCCCGGGCTCTAG	114818
rs497973	snp	A/G	0.499087	0.0213463	intron-variant, upstream-variant-2KB	KLHL29	GRCh38.p7	2:23642144	CCTCTGAGCCCCGAT[A/G]GCTGTTTGTTCGTAG	114818
rs499593	snp	A/G	0.255224	0.249945	intron-variant, nc-transcript-variant	KLHL29, LOC102723401	GRCh38.p7	2:23618340	CCAAAGATGATCCTG[A/G]GTGTGTCCGTGAGGG	114818
rs518113	snp	A/G	0.354019	0.227333	intron-variant	KLHL29	GRCh38.p7	2:23632628	TGGTCAGAGGTGCCC[A/G]CAACAAATGCACTTC	114818
rs522939	snp	A/G	0.194902	0.243853	intron-variant, nc-transcript-variant	KLHL29, LOC102723401	GRCh38.p7	2:23617167	CAACCTGGCAAATCC[A/G]AGTCTGATTTCCCGG	114818
rs527176	snp	C/G	0.498287	0.029215	intron-variant	KLHL29	GRCh38.p7	2:23643038	GGAGGGAGGGGGAAG[C/G]TGTGGAGGGCGGGAC	114818
rs528065	snp	A/G	0.498673	0.0257246	intron-variant	KLHL29	GRCh38.p7	2:23636579	CAGCTTCTTTCCCTC[A/G]AGCTGTTCATATATT	114818
rs531963	snp	C/T	0.0652144	0.168387	intron-variant	KLHL29	GRCh38.p7	2:23594143	GAGTTGATTATACAG[C/T]AGAGGTGGGAAGGTT	114818
rs535200	snp	A/G	0.216048	0.247684	intron-variant	KLHL29	GRCh38.p7	2:23646777	CAGTGATGAGATCTT[A/G]TGAAAATACTTTGAG	114818
rs538826	snp	A/G	0.453575	0.145111	intron-variant	KLHL29	GRCh38.p7	2:23613744	actccagcctgggcg[A/G]cagggcaagactcca	114818
rs540290	snp	C/G	0.499145	0.020655	intron-variant	KLHL29	GRCh38.p7	2:23639317	AGAAACGACTGAGCC[C/G]AGGGCTTGGCGGGAA	114818
rs542438	snp	C/T	0.340784	0.232934	intron-variant	KLHL29	GRCh38.p7	2:23623603	CTGGCAGACACCCCT[C/T]GGCTGGCCCCACAGA	114818
rs543012	snp	C/T	0.495671	0.0463237	intron-variant	KLHL29	GRCh38.p7	2:23639617	AGTCATGCCTTCCAG[C/T]AAGGTTTTTACTTGC	114818
rs555680	snp	C/G	0.0637235	0.166737	intron-variant	KLHL29	GRCh38.p7	2:23594428	GCTCCTGAGTGTCTG[C/G]GATTCGAACAATCCA	114818
rs562786	snp	C/T	0.498964	0.02274	intron-variant, nc-transcript-variant	KLHL29, LOC102723401	GRCh38.p7	2:23620655	GAAGTGCAGGCAGGA[C/T]ATCCAAGTGGAAGCG	114818
rs563757	snp	C/T	0.196149	0.244131	intron-variant	KLHL29	GRCh38.p7	2:23604740	ACAGAAAGGAGGACC[C/T]TCTGAGGTTAGAGGG	114818
rs564548	snp	C/T	0.19646	0.2442	intron-variant	KLHL29	GRCh38.p7	2:23614265	aaccaacctgtgccc[C/T]gaccaccctggacac	114818
rs564552	snp	A/G	0.321292	0.23962	intron-variant	KLHL29	GRCh38.p7	2:23614266	ACCAACCTGTGCCCT[A/G]ACCACCCTGGACACA	114818
rs570102	snp	C/T	0.251014	0.249998	intron-variant	KLHL29	GRCh38.p7	2:23614862	AAAGCCATCCGGTGG[C/T]GGGAAGATGTGGGCT	114818
rs573517	snp	A/G	0.495559	0.0469148	intron-variant	KLHL29	GRCh38.p7	2:23640687	AAATCATAAATATGC[A/G]TTGCACATGTATTGC	114818
rs574470	snp	A/G	0.212122	0.247114	intron-variant, upstream-variant-2KB	KLHL29	GRCh38.p7	2:23640799	GGCCTACGGTCCCTC[A/G]GCTGGGAAGGGGCGA	114818
rs577082	snp	A/G	0.461592	0.133149	intron-variant, upstream-variant-2KB	KLHL29	GRCh38.p7	2:23641073	CACCTCAGAGCAGCT[A/G]TGAAAACCAAGGTAC	114818
rs577293	snp	A/G	0.254944	0.249951	intron-variant	KLHL29	GRCh38.p7	2:23625110	TGGGAAATGTGAGCC[A/G]TGGTCATCCAGGCTG	114818
rs577843	snp	A/C	0.429688	0.173817	intron-variant	KLHL29	GRCh38.p7	2:23634574	CTCCAGGAGACTCCC[A/C]CAGGTTCCCCCAGCT	114818
rs583168	snp	A/G	0.49423	0.0534032	intron-variant	KLHL29	GRCh38.p7	2:23606275	GATTGATTCCAGAAC[A/G]TTCCCGGGCCTTGCA	114818
rs586617	snp	G/T	0.0596104	0.162024	intron-variant	KLHL29	GRCh38.p7	2:23599033	TCCTGTCCCAGGCAT[G/T]CTTTCCTATTTAAGG	114818
rs587578	snp	A/G	0.0596104	0.162024	intron-variant	KLHL29	GRCh38.p7	2:23599278	CCTGTTTCTTCATTT[A/G]TCAAGTAGGGAAAGT	114818
rs605518	snp	C/T	0.0652144	0.168387	intron-variant	KLHL29	GRCh38.p7	2:23594349	CGCAGACTTCCTGCC[C/T]GGCTCCTCCGGGCTC	114818
rs605750	snp	A/G	0.322007	0.239405	intron-variant, nc-transcript-variant	KLHL29, LOC102723401	GRCh38.p7	2:23619820	TAGTGCCTAGTTCAC[A/G]CTCCCAACTTTTCCT	114818
rs605953	snp	G/T	0.44546	0.155869	intron-variant	KLHL29	GRCh38.p7	2:23594423	CCTCCTGGATTGTTC[G/T]AATCCCAGACACTCA	114818
rs606374	snp	A/G	0.444931	0.15653	intron-variant	KLHL29	GRCh38.p7	2:23594528	AAATGGCCTTCCTGC[A/G]TTTCAATTCTCCATC	114818
rs613117	snp	A/G	0.317451	0.240729	intron-variant	KLHL29	GRCh38.p7	2:23606934	CACGATCAAGGCACC[A/G]GCCAATGTGGTGCCT	114818
rs619287	snp	C/G	0.254664	0.249956	intron-variant	KLHL29	GRCh38.p7	2:23627166	TGCCTCCTGCCGTGG[C/G]CCTCCAGTGAATTTA	114818
rs626589	snp	A/T	0.495745	0.0459295	intron-variant, upstream-variant-2KB	KLHL29	GRCh38.p7	2:23641041	TCCTCTGTCTCCCCA[A/T]CCTCAGTGTACACTG	114818
rs627973	snp	C/T	0.455263	0.142713	intron-variant	KLHL29	GRCh38.p7	2:23646701	ATTCTGGCACTGGAC[C/T]TCCACCTCATGGCAC	114818
rs635182	snp	A/G	0.254385	0.249962	intron-variant	KLHL29	GRCh38.p7	2:23628433	CGTTGTAAAGAGCCC[A/G]CTTCTTCCCCTGGGG	114818
rs642931	snp	C/T	0.335847	0.234798	synonymous-codon, upstream-variant-2KB	KLHL29	GRCh38.p7	2:23642390	CCAGCCCACCCTGAT[C/T]GCACACTCCTATGGA	114818
rs644744	snp	C/T	0.319616	0.240112	intron-variant	KLHL29	GRCh38.p7	2:23602848	GGTGCTACTCAGGCC[C/T]AGCCCAGGGGAGCCA	114818
rs647046	snp	A/G	0.194278	0.243711	intron-variant	KLHL29	GRCh38.p7	2:23603371	GGCTACAGCGGCGGC[A/G]GTCAGGGCTCTGACA	114818
rs648302	snp	A/G	0.340333	0.233109	intron-variant	KLHL29	GRCh38.p7	2:23603596	GATCTCCCTCTTTTA[A/G]AAAATCAGCACTTTC	114818
rs665650	snp	A/G	0.470034	0.11868	intron-variant	KLHL29	GRCh38.p7	2:23630630	gctaggactacaggc[A/G]cacaccaccacaccc	114818
rs667412	snp	A/G	0.348574	0.229746	intron-variant	KLHL29	GRCh38.p7	2:23624471	TTTAGCCAAAGAAAG[A/G]TGCCCTGCGACATTG	114818
rs669531	snp	A/G	0.0107246	0.0724382	intron-variant, nc-transcript-variant	KLHL29, LOC102723401	GRCh38.p7	2:23616949	TGAGCATTCTCTCTG[A/G]ATTACAGCCGTGACC	114818
rs671119	snp	A/G	0.219648	0.248151	intron-variant	KLHL29	GRCh38.p7	2:23644115	ATCTGACTGAGCCCT[A/G]ACTGCCTTTGTTTTG	114818
rs672643	snp	C/G	0.333261	0.235728	intron-variant	KLHL29	GRCh38.p7	2:23611073	CATGTTCAAAATGAT[C/G]AATGAGGAAATGCTG	114818
rs678240	snp	C/T	0.00318978	0.0398085	intron-variant	KLHL29	GRCh38.p7	2:23631111	GGCCTGGGGCCCAGA[C/T]GGGTTCTGCAGTTGT	114818
rs689184	snp	C/T	0.473081	0.112848	intron-variant	KLHL29	GRCh38.p7	2:23637862	GGCCTGCAGATGCCC[C/T]GGAGGCTCCTGTGTG	114818
rs720247	snp	G/T	0.128288	0.218372	intron-variant	KLHL29	GRCh38.p7	2:23396506	CGGCCCTTAATTTTG[G/T]TTTGAAAAGCCAGGG	114818
rs720291	snp	A/G	0.118584	0.212673	intron-variant	KLHL29	GRCh38.p7	2:23406517	AAGTGATGTTTAAGA[A/G]TAATTTTCAATTACA	114818
rs721894	snp	A/G/T	0.0437281	0.141251	intron-variant	KLHL29	GRCh38.p7	2:23397039	GACCTCTACCCAGGG[A/G/T]CCACTAGAGCAGACC	114818
rs725507	snp	C/T	0.300421	0.244863	intron-variant	KLHL29	GRCh38.p7	2:23451668	CCTCCAGGTGGGAGA[C/T]GGAGGGATTTTGGAC	114818
rs727291	snp	A/G	0.428484	0.175052	intron-variant	KLHL29	GRCh38.p7	2:23646881	CTGAGGCCCTGTGAG[A/G]GTGGTACTGTCACCC	114818
rs727936	snp	C/T	0.00755907	0.0610114	intron-variant	KLHL29	GRCh38.p7	2:23475492	TTTTTCTTTTCTTTT[C/T]TTTTTTNTGCAAAAA	114818
rs729616	snp	G/T	0.487684	0.0775019	intron-variant	KLHL29	GRCh38.p7	2:23429154	ACACGTGCGTGCCTG[G/T]GTGTATGTGAACATA	114818
rs729790	snp	A/C	0.328616	0.237317	intron-variant	KLHL29	GRCh38.p7	2:23470192	CAAAGGGCCCATCTC[A/C]TAGTTGCCTTGGATG	114818
rs731806	snp	A/G	0.486067	0.0822953	intron-variant	KLHL29	GRCh38.p7	2:23604738	CTCTAACCTCAGAAG[A/G]TCCTCCTTTCTGTCT	114818
rs732747	snp	C/G	0.486133	0.082104	intron-variant	KLHL29	GRCh38.p7	2:23604002	CAGGCCTGGGTACTG[C/G]GTGCACAGTTCTAGT	114818
rs737564	snp	C/T	0.290977	0.246619	intron-variant	KLHL29	GRCh38.p7	2:23428265	AGCTGAGTCACTCTG[C/T]GGCAAGTGGCTGTGT	114818
rs737565	snp	A/C	0.496175	0.0435625	intron-variant	KLHL29	GRCh38.p7	2:23428333	AAGGCCCATTTTCCC[A/C]CAGTGATGTTGCGAG	114818
rs737665	snp	A/G	0.396727	0.202413	intron-variant	KLHL29	GRCh38.p7	2:23668563	AGGGAGGAGGGAAGT[A/G]GTTTCAGAAGTTCCA	114818
rs744109	snp	C/T	0.485255	0.0845871	intron-variant	KLHL29	GRCh38.p7	2:23469809	TGGACCTACCAAAGC[C/T]TGACTCACCCACAGC	114818
rs747002	snp	C/T	0.456095	0.141508	intron-variant	KLHL29	GRCh38.p7	2:23486446	AATCCAGTCCCCTCA[C/T]GATGCAGATAAAAAC	114818
rs747344	snp	A/G	0.49607	0.0441545	intron-variant	KLHL29	GRCh38.p7	2:23428429	TCCTGGCACTCCATA[A/G]TCACTTTACTATGCT	114818
rs747345	snp	A/G	0.499853	0.008585	intron-variant	KLHL29	GRCh38.p7	2:23428180	AACAGAGTTTGGACC[A/G]TGTCCGCAGAAGGCC	114818
rs747622	snp	C/G	0.325563	0.238307	intron-variant	KLHL29	GRCh38.p7	2:23658596	GAGGTGGCCGTCCAT[C/G]AGGGGCCATCTCGTT	114818
rs748857	snp	C/T	0.455858	0.141853	intron-variant	KLHL29	GRCh38.p7	2:23532338	GCCAGTGAGCCGGTG[C/T]TGTCTATGTACTGCA	114818
rs748858	snp	C/T	0.49907	0.0215454	intron-variant	KLHL29	GRCh38.p7	2:23531900	CTGGATACTTTCTCA[C/T]CCTCTTTGACACCTG	114818
rs748859	snp	C/T	0.499831	0.00918375	intron-variant	KLHL29	GRCh38.p7	2:23531955	AGAACCAAGTCGCCA[C/T]GACTCCCAAGTGCCA	114818
rs748860	snp	C/T	0.499121	0.020948	intron-variant	KLHL29	GRCh38.p7	2:23532078	TCAGCAGCCTTTCCA[C/T]TGGGCCTATTCCACA	114818
rs748861	snp	A/G	0.488965	0.0734569	intron-variant	KLHL29	GRCh38.p7	2:23532210	GAGGCCATTTGACAT[A/G]TGCTGCCTGGTCTGA	114818
rs749331	snp	C/T	0.471578	0.115772	intron-variant	KLHL29	GRCh38.p7	2:23659477	AGATGAGGTTGAGGA[C/T]AAGGCTCTGGGGCTG	114818
rs749501	snp	G/T			intron-variant	KLHL29	GRCh38.p7	2:23415547	AAATCCAAAAGACTA[G/T]GACTTTAGTGCCAGA	114818
rs751313	snp	G/T	0.0655868	0.168795	intron-variant	KLHL29	GRCh38.p7	2:23683527	TCCTTTCTAAGCCTT[G/T]GGGTGGGTCTGGGAG	114818
rs751314	snp	C/G	0.0655868	0.168795	intron-variant	KLHL29	GRCh38.p7	2:23683681	GGGATCTGCCGGGCT[C/G]TAAAGCAGGCTCTGC	114818
rs763456	snp	C/T	0.384401	0.210799	intron-variant	KLHL29	GRCh38.p7	2:23452309	GACAGTAAGGCATGA[C/T]GGCTCACACCTGTAA	114818
rs763457	snp	A/T	0.35809	0.225425	intron-variant	KLHL29	GRCh38.p7	2:23452184	AAAAAAAAGAAAAAA[A/T]TTTTTTTTTCTGGGC	114818
rs815350	snp	C/G	0.200406	0.248142	intron-variant	KLHL29	GRCh38.p7	2:23593936	GATTACACAGAGCCC[C/G]GGCCTGGGAGAAGGG	114818
rs815352	snp	A/G	0.193028	0.243422	intron-variant	KLHL29	GRCh38.p7	2:23597174	TCCAATATAATAGGT[A/G]GAGAGATTGAGGTCA	114818
rs815353	snp	A/G			intron-variant	KLHL29	GRCh38.p7	2:23597315	TAtatatatatatat[A/G]tgtgtgtgtgtgtgt	114818
rs815354	snp	A/G	0	0	intron-variant	KLHL29	GRCh38.p7	2:23597383	TATATGTGTGTGTGT[A/G]TATATATATATATAT	114818
rs815356	snp	A/G	0.495559	0.0469148	intron-variant, upstream-variant-2KB	KLHL29	GRCh38.p7	2:23641710	ttgctgaggtcaggc[A/G]tggtggctcatacct	114818
rs870314	snp	C/T	0.301932	0.244547	intron-variant	KLHL29	GRCh38.p7	2:23639016	GCCTCTGACCCTGTA[C/T]TCAGTGGGCGAAGCT	114818
rs873315	snp	C/T	0.386884	0.209196	intron-variant	KLHL29	GRCh38.p7	2:23565448	GATGCTCTTTCCTTT[C/T]CTTGCTTTCTTGGGG	114818
rs873542	snp	A/C			intron-variant	KLHL29	GRCh38.p7	2:23435808	GGGTTCCAAACACCT[A/C]ACCAGGCCTTGAGGC	114818
rs873543	snp	A/G	0.093777	0.195178	intron-variant	KLHL29	GRCh38.p7	2:23435745	AGCAACTATCCCATC[A/G]CACTATGCTTACAAT	114818
rs874125	snp	G/T	0.0785177	0.181917	intron-variant	KLHL29	GRCh38.p7	2:23435153	AACATTGGAGTGTGG[G/T]CTTCAGAATGGGGAC	114818
rs874868	snp	G/T	0.475081	0.108804	intron-variant	KLHL29	GRCh38.p7	2:23575209	ACCAGAGCCGTGGAG[G/T]AGCGTTTTTGTGGTC	114818
rs876085	snp	A/T	0.489837	0.0705577	intron-variant	KLHL29	GRCh38.p7	2:23559503	CCCTTCTCCATCTGC[A/T]GCCACGACCTTCCAT	114818
rs889862	snp	C/T	0.462253	0.132093	intron-variant	KLHL29	GRCh38.p7	2:23675126	TCTCTCGGCCCTGCC[C/T]GCACCCCATGACATG	114818

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