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
rs960707	snp	A/T	0.431769	0.17164	intron-variant	KLHL12	GRCh38.p7	1:202919095	TCTCCACACAAAAAA[A/T]TTTTGTTTTAATTAG	59349
rs1042990	snp	C/T	0.495016	0.0496707	utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892438	GTCTGTTTCTCACTA[C/T]GTGCACCGGGTGATT	59349
rs1418443	snp	A/G	0.354235	0.227234	intron-variant	KLHL12	GRCh38.p7	1:202923847	TTAGTTAGTTCTATC[A/G]TCTTAGTGTAGATAT	59349
rs1539357	snp	A/T	0.495056	0.049474	intron-variant	KLHL12	GRCh38.p7	1:202909326	TTTGATCCATCTAGT[A/T]TGTTATCTATTTTTC	59349
rs1977837	snp	A/G	0.431916	0.171483	intron-variant, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202928268	TTTTTTTTTGAGACG[A/G]AGTCTTGCTCTGTCG	59349
rs1977838	snp	C/T	0.412416	0.190055	intron-variant, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202928138	ACTGGCGCCCGCCAC[C/T]ACGCCCAGCCAATTT	59349
rs2275734	snp	C/T	0.496221	0.0433033	intron-variant	KLHL12	GRCh38.p7	1:202918167	GACGAAATTCAGGTA[C/T]GGATTTGTCTTGATG	59349
rs2275739	snp	C/T	0.00500821	0.0497898	intron-variant	KLHL12	GRCh38.p7	1:202893217	ATTTAGAAACGAATC[C/T]AGACTCAATATGTAG	59349
rs2363765	snp	A/G/T	0.00119737	0.0244387	utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892431	TGCCTGTAATCACCC[A/G/T]GTGCACATAGTGAGA	59349
rs2363766	snp	A/C			synonymous-codon, utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892554	CTCGCGGAGAACACA[A/C]ACACCAGCATCACAG	59349
rs2363772	snp	A/C	0.343477	0.231866	upstream-variant-2KB	KLHL12	GRCh38.p7	1:202930233	CTTTAATGATATTGC[A/C]TAATTCCTGACTGTT	59349
rs3041271	in-del	-/CAAA	0	0	intron-variant	KLHL12	GRCh38.p7	1:202923885	CAAAAAACAAACAAA[-/CAAA]AAACTTGTGCTTAAA	59349
rs3182429	snp	A/G	0.390694	0.206652	synonymous-codon	KLHL12	GRCh38.p7	1:202919819	TGTGTACACAGAAAC[A/G]GTACATGTGACAGTG	59349
rs3737886	snp	A/G	0	0	intron-variant	KLHL12	GRCh38.p7	1:202925335	ATGCCAGGCATAGGA[A/G]TGCCCTCAACTTGTG	59349
rs3766570	snp	A/G	0.00302808	0.0387926	intron-variant	KLHL12	GRCh38.p7	1:202909171	TTGTACTCTTATAGT[A/G]TTACAGGTATCCCCA	59349
rs3766571	snp	C/T	0.0460142	0.144533	downstream-variant-500B, upstream-variant-2KB	KLHL12, RABIF	GRCh38.p7	1:202890963	ACAGGTAAGAGGTAG[C/T]CACTTTACACTTTGG	59349
rs3766572	snp	A/G	0.433818	0.169443	downstream-variant-500B, upstream-variant-2KB	KLHL12, RABIF	GRCh38.p7	1:202890939	ACTTTGGAGATTCTC[A/G]TCAGTAAAATATTTA	59349
rs3820152	snp	A/T	0.494733	0.0510469	intron-variant	KLHL12	GRCh38.p7	1:202909364	GAAATACTGCTCAAC[A/T]TATCTGTTTATATCA	59349
rs3841739	in-del	-/G			intron-variant, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202927287	ACTCTGGAGCGGGGG[-/G]AGGGCGGTGCTCCAG	59349
rs4081384	snp	A/G			utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892469	TAGTGGGAGAATCAA[A/G]AATCCTTTCCAGAAT	59349
rs4388755	snp	G/T	0.103438	0.202533	upstream-variant-2KB	KLHL12	GRCh38.p7	1:202930413	TTTTTTCTTCTTTTA[G/T]TTCCTCTTTTTTGTT	59349
rs4950869	snp	C/G	0.118933	0.212888	utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892437	TAATCACCCGGTGCA[C/G]ATAGTGAGAAACAGA	59349
rs4950887	snp	C/T	0.35445	0.227135	intron-variant	KLHL12	GRCh38.p7	1:202901202	TTTTCCCAATAAACA[C/T]TCTGGTAACTATATG	59349
rs4950888	snp	C/T	0.495135	0.0490805	intron-variant	KLHL12	GRCh38.p7	1:202903497	caaggtcttgctctg[C/T]tgcccaggctagagt	59349
rs4950889	snp	C/T	0.494774	0.0508504	intron-variant	KLHL12	GRCh38.p7	1:202905658	gtaatatctgcatta[C/T]ttctttgcacaacta	59349
rs4950890	snp	C/G	0.293294	0.246223	intron-variant	KLHL12	GRCh38.p7	1:202915104	ATTTTCTCCACAATA[C/G]ATTTTCACAAAGAAT	59349
rs6427976	snp	G/T	0.046775	0.145601	utr-variant-3-prime	KLHL12	GRCh38.p7	1:202891611	ATTTGATCCAACAAA[G/T]AAAGGCTTTCACCCC	59349
rs6427977	snp	A/G	0.349671	0.229272	intron-variant	KLHL12	GRCh38.p7	1:202895221	ACATGGCGAAACCCC[A/G]TCTCTACTAAAAATA	59349
rs6427978	snp	A/G	0.351853	0.228311	intron-variant	KLHL12	GRCh38.p7	1:202897287	GTTGACCAGGCTAGA[A/G]TGCAATTCCATGATC	59349
rs6427979	snp	C/T	0.492337	0.0614248	intron-variant	KLHL12	GRCh38.p7	1:202900375	atggtgagactccca[C/T]atctagaaaaaaata	59349
rs6662398	snp	G/T	0.495174	0.0488838	intron-variant	KLHL12	GRCh38.p7	1:202919328	TGAAAATATCATACT[G/T]TAATATTTTGTGCAT	59349
rs6662413	snp	C/T	0.494774	0.0508504	intron-variant	KLHL12	GRCh38.p7	1:202919368	TTTCATGTATCTTAA[C/T]GAAATACTACCACTT	59349
rs6667300	snp	C/T	0.300169	0.244914	intron-variant	KLHL12	GRCh38.p7	1:202924791	TACTATTATCCCTAA[C/T]TTAAAGATGAGGAAA	59349
rs6685274	snp	C/G	0.291493	0.246533	intron-variant	KLHL12	GRCh38.p7	1:202910167	AGAACCTATGAGGAA[C/G]GTACTATTATCATCC	59349
rs6686801	snp	C/T	0.492386	0.0612297	intron-variant	KLHL12	GRCh38.p7	1:202905602	tatctgaaatgctta[C/T]gacaagaagcgctac	59349
rs6686804	snp	C/T	0.34989	0.229177	intron-variant	KLHL12	GRCh38.p7	1:202905612	gcttacgacaagaag[C/T]gctacagatttcaga	59349
rs6692075	snp	C/T	0.494568	0.0518327	intron-variant	KLHL12	GRCh38.p7	1:202912174	CACTGAAGAACATCA[C/T]CTAAGAGATAATTTG	59349
rs7516884	snp	A/G	0.0103295	0.0711199	intron-variant	KLHL12	GRCh38.p7	1:202905014	CTGGTTTAGCAGCCA[A/G]TATGCATAGAGATGG	59349
rs7520522	snp	C/T	0.111224	0.207945	intron-variant	KLHL12	GRCh38.p7	1:202920079	agcactttgagaggc[C/T]aaggcaggcaaatca	59349
rs7523420	snp	G/T	0.0535932	0.154675	intron-variant	KLHL12	GRCh38.p7	1:202896576	GCACGACCAATGAAA[G/T]GTGCTAGGAATTATA	59349
rs7530468	snp	C/G	0.431621	0.171796	intron-variant	KLHL12	GRCh38.p7	1:202902453	AACACCAAAAACAAA[C/G]AAACAAAAAAACCTA	59349
rs7531745	snp	A/G	0.354235	0.227234	downstream-variant-500B, upstream-variant-2KB	KLHL12, RABIF	GRCh38.p7	1:202890640	GTTTAATTAGCATGC[A/G]CAATCCATCTGCCAA	59349
rs7532610	snp	C/T	0	0	intron-variant	KLHL12	GRCh38.p7	1:202908309	cccaaccagtcattg[C/T]tggggcttggatttg	59349
rs7536140	snp	C/T	0.433236	0.170072	intron-variant	KLHL12	GRCh38.p7	1:202909680	GCTCAGAAGACTGGC[C/T]TATATGAACTGTGTC	59349
rs7542125	snp	C/T	0.431769	0.17164	intron-variant	KLHL12	GRCh38.p7	1:202902110	TGTAACATAATTTCC[C/T]TCCAGCCTTGTTTCT	59349
rs7542327	snp	C/T	0.300421	0.244863	intron-variant	KLHL12	GRCh38.p7	1:202902361	CTTGAACTTGGGAAG[C/T]GGAGACTGCAGTGAG	59349
rs7543722	snp	A/T	0.0228947	0.104514	intron-variant	KLHL12	GRCh38.p7	1:202899832	catctcaaaaaaaaa[A/T]aaaaaaaataataat	59349
rs7543724	snp	A/T	0.0228947	0.104514	intron-variant	KLHL12	GRCh38.p7	1:202899838	aaaaaaaaaaaaaaa[A/T]aataataataataaa	59349
rs7548635	snp	A/G			intron-variant	KLHL12	GRCh38.p7	1:202906380	gaatcgcttgaaccc[A/G]ggagacagaggttgc	59349
rs7548700	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202906403	gaggttgcagtgagc[A/C]aagattatgccactg	59349
rs8179338	snp	A/G	0.300169	0.244914	intron-variant	KLHL12	GRCh38.p7	1:202913175	ATCTGGGGAACTTAG[A/G]TCTAAGCATACATAT	59349
rs9651059	snp	C/G	0.433236	0.170072	intron-variant	KLHL12	GRCh38.p7	1:202916806	CAACACAGCGAGACC[C/G]CATCTCAACAAAAAT	59349
rs9700677	snp	C/T	0.428635	0.174898	intron-variant	KLHL12	GRCh38.p7	1:202899776	TGCAGTGAGCCGAGA[C/T]TGCACCACTGCACTC	59349
rs9919219	snp	C/T	0.300169	0.244914	intron-variant	KLHL12	GRCh38.p7	1:202908269	TTAGTGGTAGACATA[C/T]AGGCTCAGATAAATT	59349
rs9943282	snp	C/T	0.492337	0.0614248	intron-variant	KLHL12	GRCh38.p7	1:202926012	AAGAAGGCTGAGGCC[C/T]GAGAATCACTTGAAC	59349
rs10577552	in-del	-/TCTC			intron-variant	KLHL12	GRCh38.p7	1:202911457	ATATATATATATGTA[-/TCTC]TCTCTCTCTCTCTCT	59349
rs10612618	in-del	-/AA	0.0228947	0.104514	intron-variant	KLHL12	GRCh38.p7	1:202899823	GTAAGACTCCATCTC[-/AA]AAAAAAAAAAAAAAA	59349
rs10641768	in-del	-/CCT	0	0	intron-variant	KLHL12	GRCh38.p7	1:202917456	GACACAAGCAGTTCT[-/CCT]GCCTCAGCCTCCCAA	59349
rs10732291	snp	A/G	0.495174	0.0488838	intron-variant	KLHL12	GRCh38.p7	1:202922040	CATTTAATAATTATG[A/G]TACTGAAATATGTAA	59349
rs10732292	snp	C/T	0.492386	0.0612297	intron-variant	KLHL12	GRCh38.p7	1:202922238	ATTCTCACAGCAACC[C/T]GGTAAGGTAGTTAGG	59349
rs10753926	snp	C/T	0.495174	0.0488838	intron-variant	KLHL12	GRCh38.p7	1:202906957	GTGAGACACCGTGCC[C/T]GGCCTGTTACATATA	59349
rs10753927	snp	C/T	0.304438	0.244001	intron-variant	KLHL12	GRCh38.p7	1:202912481	TGGTGGTGGATATGG[C/T]GGCAGTGAGGATGGC	59349
rs10753928	snp	A/C	0.495174	0.0488838	intron-variant	KLHL12	GRCh38.p7	1:202921917	AAAATCAATCCCTAA[A/C]ACTAAAAAAGTCACT	59349
rs10800877	snp	C/T	0.41325	0.18934	intron-variant	KLHL12	GRCh38.p7	1:202914935	GAAAGAAATCTGTAA[C/T]TGATTGTGGTCAACA	59349
rs10800878	snp	C/G	0.354235	0.227234	intron-variant	KLHL12	GRCh38.p7	1:202920277	CAAGATTGTGCCACT[C/G]CACTCCAGCCTGGGC	59349
rs10800879	snp	C/T	0	0	intron-variant	KLHL12	GRCh38.p7	1:202921165	ACAGGAGTACACCAC[C/T]ACAACCAGCTAATTT	59349
rs10800880	snp	C/T	0.413748	0.188909	intron-variant	KLHL12	GRCh38.p7	1:202923789	CATAAAAGGTAGTTA[C/T]TACCATCACAGAATA	59349
rs10800881	snp	A/T	0.356169	0.226336	intron-variant	KLHL12	GRCh38.p7	1:202925612	TTTAGAGCATACATA[A/T]AAAGAGGATCCTGCT	59349
rs10800882	snp	A/G	0.496314	0.0427728	intron-variant, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202928303	AGAAAAAAGAAAAAA[A/G]AGAAAAAACAAAAAA	59349
rs10920519	snp	A/C	0.413748	0.188909	intron-variant	KLHL12	GRCh38.p7	1:202897203	AGAAAGCAAACTTCA[A/C]CATGACACTGCACCA	59349
rs10920521	snp	C/T	0.356383	0.226236	intron-variant	KLHL12	GRCh38.p7	1:202916419	AGCATTTTAGGAGGC[C/T]GAAGTGGCTGATGTC	59349
rs10920522	snp	A/G	0.333491	0.235646	intron-variant	KLHL12	GRCh38.p7	1:202923092	TGGACTCTCTCCTTT[A/G]AACAATTACTCTCAA	59349
rs10920523	snp	G/T	0.495095	0.0492773	intron-variant	KLHL12	GRCh38.p7	1:202923146	ATTTCCTTGCCTGAT[G/T]TCAGTTTTTAAAGAA	59349
rs10920524	snp	G/T	0.495095	0.0492773	intron-variant	KLHL12	GRCh38.p7	1:202923147	TTTCCTTGCCTGATG[G/T]CAGTTTTTAAAGAAA	59349
rs10920525	snp	C/T	0.119281	0.213102	intron-variant	KLHL12	GRCh38.p7	1:202924586	gcaacatagtgagac[C/T]ctgtctctacaaata	59349
rs10920526	snp	C/T			intron-variant, upstream-variant-2KB, splice-acceptor-variant	KLHL12	GRCh38.p7	1:202927516	GGCAAAACCCCGTTT[C/T]TACAAAAAAAAAAAA	59349
rs10920527	snp	A/C			intron-variant, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202927518	CAAAACCCCGTTTCT[A/C]CAAAAAAAAAAAAAA	59349
rs11305071	in-del	-/T	0	0	intron-variant	KLHL12	GRCh38.p7	1:202897229	TTTTTTTTTTTTTTT[-/T]GGAGACAGAGTTTCG	59349
rs11366890	in-del	-/T	0.34989	0.229177	intron-variant	KLHL12	GRCh38.p7	1:202900919	GTGTGGTGGTGTGCA[-/T]TTTGTAGTCCCAGCT	59349
rs11403422	in-del	-/A	0	0	intron-variant, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202928282	CAAAAAAAAAAAAAA[-/A]GAAAAAAGAAAAAAG	59349
rs11404714	in-del	-/T	0.485187	0.0847778	intron-variant	KLHL12	GRCh38.p7	1:202903460	TCTTGTTTTTTTTTT[-/T]CTTTTTTGAGACAAG	59349
rs11584998	snp	A/C			intron-variant	KLHL12	GRCh38.p7	1:202923859	AGATGATAGAACTAA[A/C]TAAAAAAAAAACAAA	59349
rs11801140	snp	G/T	0	0	intron-variant	KLHL12	GRCh38.p7	1:202921808	CTTAAAAAACTCTGG[G/T]GCATCTCCATTATTA	59349
rs11806328	snp	A/G	0.0023933	0.0345097	intron-variant	KLHL12	GRCh38.p7	1:202892743	actatgcaggaggct[A/G]aggtaagaggattgc	59349
rs11809627	snp	A/T	0.5	0	intron-variant	KLHL12	GRCh38.p7	1:202901474	ttttttttttttttt[A/T]aattttttaaagaga	59349
rs11811101	snp	A/T			intron-variant	KLHL12	GRCh38.p7	1:202901476	tttttttttttttta[A/T]ttttttaaagagagg	59349
rs12034646	snp	C/T	0	0	missense	KLHL12	GRCh38.p7	1:202919902	AAGGTTTCCCCTTCT[C/T]TGAGAGCTGAAAATT	59349
rs12037706	snp	A/C	0.0182019	0.0936463	intron-variant	KLHL12	GRCh38.p7	1:202923074	gcctagaatccaggt[A/C]tctggactctcTCCT	59349
rs12043834	snp	C/T	0.118933	0.212888	intron-variant	KLHL12	GRCh38.p7	1:202906526	gagtttattgtttaa[C/T]gggtacagagtttca	59349
rs12067508	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202903624	accacTAAttttttt[C/T]ttttctttttttttt	59349
rs12067510	snp	C/T			intron-variant	KLHL12	GRCh38.p7	1:202903629	TAAtttttttctttt[C/T]tttttttttttgaaa	59349
rs12070941	snp	C/T	0.433236	0.170072	intron-variant	KLHL12	GRCh38.p7	1:202916500	AAATACAAAAATTAG[C/T]TGGTGTAGTGGTGGG	59349
rs12074142	snp	C/T	0.00199481	0.0315187	intron-variant	KLHL12	GRCh38.p7	1:202913324	TGCCCCTTCTACCAG[C/T]CCCTACAGAGTACAT	59349
rs12089566	snp	A/G	0.433382	0.169915	utr-variant-3-prime	KLHL12	GRCh38.p7	1:202892214	CATATGAGGCACAAC[A/G]TACATATAGTACACC	59349
rs12091309	snp	A/G	0.0185938	0.0946107	intron-variant	KLHL12	GRCh38.p7	1:202916416	ctcagcattttagga[A/G]gctgaagtggctgat	59349
rs12092574	snp	C/G			intron-variant	KLHL12	GRCh38.p7	1:202916972	agtgagaccatctca[C/G]aagaaaaaaaaaaaa	59349
rs12094608	snp	A/T	0.11963	0.213316	intron-variant	KLHL12	GRCh38.p7	1:202904377	TGTATATGATTTTTT[A/T]ATTTATTCAAATATG	59349
rs12117507	snp	C/G			intron-variant, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202927836	aatacaaaaaaatta[C/G]ccgggcgttgtggca	59349
rs12118311	snp	A/G			intron-variant, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202927892	gaggctaatgcagga[A/G]aatcgctagaacctg	59349
rs12118322	snp	A/G	0	0	intron-variant, upstream-variant-2KB	KLHL12	GRCh38.p7	1:202927969	tgggcgaccgactga[A/G]actctgtctcttaaa	59349

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