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
rs3675141	snp	A/G	0.433884	0.169371	intron-variant	Klhl12	GRCm38.p3	1:134474325	TGAATCAGTCTTTAC[A/G]TTATGTTTTAGTACA	240756
rs3675178	snp	C/T	0.456747	0.140554	intron-variant	Klhl12	GRCm38.p3	1:134474347	TTTAGTACAGAGATC[C/T]GGAGCTAGAATCAGG	240756
rs3676898	snp	A/G	0.408163	0.193609	intron-variant	Klhl12	Mm_Celera	1:134474602	TTTATATGAGTTGAC[A/G]ATTCCAACAGGAAAC	240756
rs13465052	snp	A/C	0.5	0	utr-variant-3-prime	Klhl12	GRCm38.p3	1:134490183	GATTTCACAGTCTTT[A/C]TAATGTAAAATGTTG	240756
rs30476148	snp	A/G	0.375	0.216506	intron-variant	Klhl12	GRCm38.p3	1:134464361	TCCAGAAGCATCTGT[A/G]TTTGATTCCCAGCAC	240756
rs30557075	snp	A/T	0.375	0.216506	intron-variant	Klhl12	GRCm38.p3	1:134475267	TAGAGCACCAGTGGG[A/T]ATAGATGTGGGAGTT	240756
rs30566721	snp	C/T	0.444444	0.157135	intron-variant	Klhl12	GRCm38.p3	1:134475612	CAGAAATCCTTTTAT[C/T]TCAGCCTGCCAAGTA	240756
rs30570954	snp	G/T	0.387812	0.208586	intron-variant	Klhl12	GRCm38.p3	1:134483663	ACAACAGTTTCCTGT[G/T]TGAACCTTTCTACTT	240756
rs30619476	snp	C/T	0.375	0.216506	intron-variant	Klhl12	GRCm38.p3	1:134469842	ATCAGAAACTGTGGC[C/T]CAGAGGTAAACCCTC	240756
rs30665898	snp	C/T	0.401235	0.199068	intron-variant	Klhl12	GRCm38.p3	1:134458816	TTGCTGTCACTGTCA[C/T]GTGTGTCTTCTGAAG	240756
rs30748688	snp	A/G	0.32	0.24	intron-variant	Klhl12	GRCm38.p3	1:134485515	CAGTAGAAAGCCATG[A/G]TGTCTTATATAAACT	240756
rs30816406	snp	A/T	0.432133	0.171253	intron-variant	Klhl12	GRCm38.p3	1:134462768	TGCATAGCTTAGAGC[A/T]GCTCTCGATCACTGC	240756
rs30856115	snp	C/T	0.375	0.216506	intron-variant	Klhl12	GRCm38.p3	1:134480978	AGAGCACTTGCCTAG[C/T]ATAGGAGAGCCTGGG	240756
rs30867294	snp	C/T	0.429688	0.173817	intron-variant	Klhl12	GRCm38.p3	1:134485335	TAAGTCTCATTTCAG[C/T]ATTCAGTACTTTACA	240756
rs30867295	snp	A/T	0.432133	0.171253	intron-variant	Klhl12	GRCm38.p3	1:134485234	AGCTGCCACCACCAT[A/T]AAGGCTGCACAACTT	240756
rs30867296	snp	A/G	0.124444	0.216185	intron-variant	Klhl12	Mm_Celera	1:134485190	AAAAAAATTCTCACC[A/G]CAGAAGTGTCAGTAA	240756
rs30867297	snp	A/G	0.231111	0.249285	intron-variant	Klhl12	Mm_Celera	1:134484818	TCCTGAGCCAGGGTT[A/G]CACACGGAGCCACCA	240756
rs30867298	snp	A/C	0.124444	0.216185	intron-variant	Klhl12	Mm_Celera	1:134484781	CCCTGGCTGGCCTCA[A/C]GCTTACAGGCTTTCC	240756
rs30867299	snp	G/T	0.132653	0.220748	intron-variant	Klhl12	Mm_Celera	1:134484215	ACACATGTGGGCATG[G/T]CTGTGCCATAGCCAT	240756
rs30867300	snp	C/T	0.124444	0.216185	intron-variant	Klhl12	Mm_Celera	1:134484100	GAATGCATGTCCCTT[C/T]CAGCCATGCTGTAGC	240756
rs30867301	snp	A/G	0.459184	0.136902	intron-variant	Klhl12	GRCm38.p3	1:134484044	GTCCCTTCCAGCCAT[A/G]CTGTAGCAGAATGCA	240756
rs30867302	snp	C/T	0.231111	0.249285	intron-variant	Klhl12	Mm_Celera	1:134483945	TGAGAGTAGAAAAGC[C/T]TCAGAACAGCAGAAT	240756
rs30867303	snp	A/T	0.124444	0.216185	intron-variant	Klhl12	Mm_Celera	1:134483908	TCATTGGCTCCTGAC[A/T]CTAGCTCATATGTGA	240756
rs30868204	snp	A/G	0.124444	0.216185	intron-variant	Klhl12	Mm_Celera	1:134483861	TTTTACCAGTAAGTC[A/G]TGGTGGAACCATTTC	240756
rs30868205	snp	A/G	0.124444	0.216185	intron-variant	Klhl12	Mm_Celera	1:134483648	TGCCTCCAAAAGAAG[A/G]CAACAGTTTCCTGTG	240756
rs30868206	snp	A/G	0.32	0.24	intron-variant	Klhl12	Mm_Celera	1:134483340	CAAACACATGGAAAC[A/G]TAAAATAAAATATAG	240756
rs30868207	snp	A/T	0.124444	0.216185	intron-variant	Klhl12	Mm_Celera	1:134483296	ACATACACAATACAT[A/T]CATTCAAACCTATAC	240756
rs30868208	snp	C/T	0.375	0.216506	intron-variant	Klhl12	GRCm38.p3	1:134482927	CACCAATGGAGTGGT[C/T]GTAAGGGCCTGGGAC	240756
rs30868209	snp	A/G	0.408163	0.193609	intron-variant	Klhl12	GRCm38.p3	1:134482331	GAGATCTGCCTGTCC[A/G]ATCTGCTACTTGACT	240756
rs30868210	snp	A/G	0.132653	0.220748	intron-variant	Klhl12	Mm_Celera	1:134482253	TTGAGTTCAGGAACT[A/G]GAAATACAGAGGAAC	240756
rs30868211	snp	A/G	0.336735	0.234472	intron-variant	Klhl12	Mm_Celera	1:134482178	TGATCATATCCCTAT[A/G]GTGTCATTTATCATG	240756
rs30868212	snp	A/G	0.277778	0.248452	intron-variant	Klhl12	Mm_Celera	1:134482123	AATGTAACAAATAAT[A/G]GCTAAAAAAAAAATC	240756
rs30868213	snp	A/G	0.142012	0.225474	intron-variant	Klhl12	Mm_Celera	1:134481553	GCCTTTAACAGCTAA[A/G]CTATTTCTAAAGCCC	240756
rs30869144	snp	C/G	0.124444	0.216185	intron-variant	Klhl12	Mm_Celera	1:134481319	TGCCTGGCGAGAGAC[C/G]TGTTCTTAAAAACAA	240756
rs30869145	snp	A/G	0.231111	0.249285	intron-variant	Klhl12	Mm_Celera	1:134480475	ATCCATGTAAAGTGG[A/G]TTAAGTTCACCCACT	240756
rs30869146	snp	C/T	0.231111	0.249285	intron-variant	Klhl12	Mm_Celera	1:134480455	TCCTCTGAGCCACAG[C/T]GTGTATCCATGTAAA	240756
rs30869147	snp	A/G/T	0.132653	0.220748	intron-variant	Klhl12	Mm_Celera	1:134480370	CAAGTGCTGTTGCAC[A/G/T]GAGCTGTGTCCCTTA	240756
rs30869148	snp	C/T	0.231111	0.249285	intron-variant	Klhl12	Mm_Celera	1:134480279	TCAGTAGACCTCTGT[C/T]CCTAATTTTATATAT	240756
rs30869149	snp	C/T	0.124444	0.216185	intron-variant	Klhl12	Mm_Celera	1:134480118	GTTTGTTTATTTACA[C/T]ACTTCAGCATTAGTC	240756
rs30869150	snp	A/C	0.231111	0.249285	intron-variant	Klhl12	Mm_Celera	1:134480009	CCCTTAAAAGGCAGG[A/C]GCTCTTGAATACTTA	240756
rs30869151	snp	A/G	0.42	0.183303	intron-variant	Klhl12	Mm_Celera	1:134479986	GGACCCTCCTGTTTG[A/G]TCCTCAGCCCTTAAA	240756
rs30869152	snp	C/G	0.124444	0.216185	intron-variant	Klhl12	Mm_Celera	1:134479975	AGCCTCCAGTGGGAC[C/G]CTCCTGTTTGGTCCT	240756
rs30869153	snp	C/T	0.231111	0.249285	intron-variant	Klhl12	Mm_Celera	1:134479915	CTAAGGGAAAAAAAA[C/T]CATTTTTGAAAATGG	240756
rs30869824	snp	C/G	0.32	0.24	intron-variant	Klhl12	GRCm38.p3	1:134479647	CTTACTATGTATTGA[C/G]TGCAGTGGTGGGAGG	240756
rs30869825	snp	A/G	0.432133	0.171253	intron-variant	Klhl12	GRCm38.p3	1:134479567	GTTATACCATGGGTG[A/G]CCTGGCACCAAGAGA	240756
rs30869826	snp	A/G	0.32	0.24	intron-variant	Klhl12	GRCm38.p3	1:134479435	AGGATAATCGCCGGT[A/G]TATCCAGTATATAAG	240756
rs30869827	snp	A/C	0.231111	0.249285	intron-variant	Klhl12	Mm_Celera	1:134479382	CATATAAACCATGTA[A/C]TACCTTTATCCTGAG	240756
rs30869828	snp	C/G	0.231111	0.249285	intron-variant	Klhl12	Mm_Celera	1:134479360	TATTGCTGAGCCACG[C/G]TGAAATCATATAAAC	240756
rs30869829	snp	C/T	0.231111	0.249285	intron-variant	Klhl12	Mm_Celera	1:134479133	TTAGGGAATTTGTTT[C/T]ATTTTGTTATTTTTA	240756
rs30869830	snp	A/G	0.244898	0.249948	intron-variant	Klhl12	GRCm38.p3	1:134478744	GAGAGGTAGAAAAAA[A/G]AATTGGAGCTTGAGA	240756
rs30869831	snp	A/G	0.32	0.24	intron-variant	Klhl12	GRCm38.p3	1:134478620	TCCTGCCCACCTCCT[A/G]TGCTTTTTAGTGTCA	240756
rs30869832	snp	C/T	0.432133	0.171253	intron-variant	Klhl12	Mm_Celera	1:134477621	GGTCCCTATTACTGC[C/T]CTGTAAAAAGAGCCT	240756
rs30869833	snp	C/T	0.297521	0.245442	intron-variant	Klhl12	Mm_Celera	1:134477588	GGCACAGAGTAAATA[C/T]TTAGCTATTTTTATC	240756
rs30870584	snp	A/G	0.444444	0.157135	intron-variant	Klhl12	GRCm38.p3	1:134477235	AATCAAAGCCCTGCC[A/G]GTGGCTAATTAGTGA	240756
rs30870585	snp	A/G	0.231111	0.249285	intron-variant	Klhl12	Mm_Celera	1:134476073	TATTTCCTGTTGTTT[A/G]AGAGTGTCTTTGTGG	240756
rs30870586	snp	A/G	0.124444	0.216185	synonymous-codon	Klhl12	Mm_Celera	1:134475853	GAAGTTTCACCTGAG[A/G]CCTGAACTTCGGAGT	240756
rs30870587	snp	A/G	0.345679	0.230967	intron-variant	Klhl12	GRCm38.p3	1:134475727	ATTGCTTCTTTATAT[A/G]CCTCATTTTGTTATT	240756
rs30870588	snp	A/G	0.197531	0.244432	intron-variant	Klhl12	Mm_Celera	1:134475449	GAGGAGAACAAAGGA[A/G]GGAAGGAGAGAGAGA	240756
rs30870589	snp	C/G	0.124444	0.216185	intron-variant	Klhl12	Mm_Celera	1:134474981	AGAGAGCAAAGTACA[C/G]AGTGGAGGTAGATGC	240756
rs30870590	snp	C/T	0.444444	0.157135	intron-variant	Klhl12	GRCm38.p3	1:134474951	GCGGTTTATAGGGAC[C/T]GTTTTTTCTGAACTA	240756
rs30870591	snp	C/T	0.32	0.24	intron-variant	Klhl12	GRCm38.p3	1:134474898	TGCCCTGCAGCAGAA[C/T]TCATCCCAGCTAGGA	240756
rs30870592	snp	A/T	0.231111	0.249285	intron-variant	Klhl12	Mm_Celera	1:134474791	GACAGTGGAGACTAC[A/T]GATCTAGAACAACCA	240756
rs30870593	snp	A/G	0.124444	0.216185	intron-variant	Klhl12	Mm_Celera	1:134473659	TTTAGGTGAAGCCCA[A/G]TAACTTCTTGGCCAG	240756
rs30870794	snp	A/G	0.124444	0.216185	intron-variant	Klhl12	Mm_Celera	1:134462712	GCCCTAGGGCTCTGA[A/G]GTTTTGCTATTACGA	240756
rs30870795	snp	C/T	0.336735	0.234472	intron-variant	Klhl12	GRCm38.p3	1:134461534	ACAGTCCTGCTGAAA[C/T]AGGACGTGTCCTGCT	240756
rs30870796	snp	G/T	0.124444	0.216185	intron-variant	Klhl12	Mm_Celera	1:134461407	CAGCACAGATCTCTA[G/T]CTTGTAGTGTTCTTC	240756
rs30870797	snp	A/C	0.124444	0.216185	intron-variant	Klhl12	Mm_Celera	1:134461295	AAAAATGATTCTTAA[A/C]TGCCATTTCAGCCAT	240756
rs30870798	snp	A/G	0.152778	0.230321	intron-variant	Klhl12	Mm_Celera	1:134461274	CCTCTACAGCATGTG[A/G]CTGTAAAAAATGATT	240756
rs30870799	snp	C/T	0.401235	0.199068	intron-variant	Klhl12	GRCm38.p3	1:134461268	GCTTTGCCTCTACAG[C/T]ATGTGGCTGTAAAAA	240756
rs30870800	snp	A/G	0.124444	0.216185	intron-variant	Klhl12	Mm_Celera	1:134460309	ATGAATAATTATCAC[A/G]TGTTTAAACTTAGAC	240756
rs30870801	snp	C/T	0.444444	0.157135	intron-variant	Klhl12	Mm_Celera	1:134459892	AGACAGACAGACAGA[C/T]AGCAAGCTGGTTCAA	240756
rs30870802	snp	A/G	0.124444	0.216185	intron-variant	Klhl12	Mm_Celera	1:134459784	TACACAAAGCCACGA[A/G]ATTAAGACCATCCTT	240756
rs30870803	snp	A/G	0.391111	0.206368	intron-variant	Klhl12	GRCm38.p3	1:134459543	AAATCATCAATAATT[A/G]TAGAAAATGAGTATG	240756
rs30871624	snp	A/G	0.489796	0.070696	intron-variant	Klhl12	GRCm38.p3	1:134473284	acacacacacacaca[A/G]TGTTGCGTGGACTGT	240756
rs30871625	snp	A/G	0.124444	0.216185	intron-variant	Klhl12	Mm_Celera	1:134473121	ATTTGTCAGACCCTC[A/G]TGGTTTTACTTCTAG	240756
rs30871626	snp	C/T	0.32	0.24	intron-variant	Klhl12	GRCm38.p3	1:134472588	AAACTCCACTAACTC[C/T]GCAGCCTAGCTACTC	240756
rs30871627	snp	A/G	0.124444	0.216185	intron-variant	Klhl12	Mm_Celera	1:134472564	TCACATAAGGCGCTT[A/G]GCATCCAGAAACTCC	240756
rs30871628	snp	A/G	0.231111	0.249285	intron-variant	Klhl12	Mm_Celera	1:134471924	TTCAGAGGCAACTAC[A/G]AATGAAAATTATTTC	240756
rs30871629	snp	A/G	0.231111	0.249285	intron-variant	Klhl12	Mm_Celera	1:134471848	AGTAGTTGCTGAAAT[A/G]CTGACTGAACATACT	240756
rs30871630	snp	C/T	0.231111	0.249285	intron-variant	Klhl12	Mm_Celera	1:134471755	AGAGTGCTTCTTACT[C/T]TATCTATCTATCGTG	240756
rs30871631	snp	A/T	0.231111	0.249285	intron-variant	Klhl12	Mm_Celera	1:134471672	TCCTGCACCTACGTG[A/T]CTGCCTTTGGGAAGT	240756
rs30871632	snp	C/G	0.231111	0.249285	intron-variant	Klhl12	Mm_Celera	1:134471652	GATTGCTGAGAGAGC[C/G]TGGGTCCTGCACCTA	240756
rs30871633	snp	A/C	0.48	0.0979796	intron-variant	Klhl12	GRCm38.p3	1:134471624	ATGAGGCCTTGGGTT[A/C]CATCTGCCTAGAGAT	240756
rs30871634	snp	C/T	0.408163	0.193609	intron-variant	Klhl12	Mm_Celera	1:134459093	AAAAAGTCTGGTAAA[C/T]CAGTGAATCTGTATA	240756
rs30871635	snp	C/T	0.124444	0.216185	intron-variant	Klhl12	GRCm38.p3	1:134458754	AATAGCATGTGTTGG[C/T]GATTCAGCTATGGCA	240756
rs30871636	snp	A/G	0.375	0.216506	intron-variant	Klhl12	Mm_Celera	1:134456246	GGTGGAACATCCCAA[A/G]TACAGTTTTACAGAT	240756
rs30871637	snp	A/C	0.375	0.216506	upstream-variant-2KB	Klhl12	Mm_Celera	1:134455273	TAGAGAACTCTGAAA[A/C]CCCGTGGGTCTCCCG	240756
rs30871638	snp	C/T	0.375	0.216506	upstream-variant-2KB	Klhl12	Mm_Celera	1:134455190	GGCACATTTAGGACC[C/T]TGTGGTTATCCGGGA	240756
rs30871639	snp	C/T	0.375	0.216506	upstream-variant-2KB	Klhl12	Mm_Celera	1:134454790	AAATGTCAGGAACAG[C/T]TTGGGATCAAGAAGC	240756
rs30871640	snp	C/T	0.444444	0.157135	upstream-variant-2KB	Klhl12	Mm_Celera	1:134454651	GGGGAAGCATTCCTG[C/T]CCTGAAGTCTGATGA	240756
rs30871916	snp	A/C	0.391111	0.206368	downstream-variant-500B	Klhl12	GRCm38.p3	1:134490951	AAGGTCTTTCATCTA[A/C]CCTGTTTACCTTATG	240756
rs30871917	snp	C/T	0.42	0.183303	utr-variant-3-prime	Klhl12	GRCm38.p3	1:134490683	AATGGCAGTTCTAGG[C/T]ACCTCTGTGTCGTGG	240756
rs30871918	snp	C/T	0.297521	0.245442	utr-variant-3-prime	Klhl12	GRCm38.p3	1:134490547	CTGCTGTGTGTGGTA[C/T]GTTCAGTTTTCTTCC	240756
rs30871919	snp	C/T	0.124444	0.216185	utr-variant-3-prime	Klhl12	Mm_Celera	1:134490395	AGACCATCTTCCTGG[C/T]GAATCAAGTGCTACC	240756
rs30871920	snp	G/T	0.495868	0.0452663	utr-variant-3-prime	Klhl12	Mm_Celera	1:134490155	TTGGAAGGCTGGAAA[G/T]GACATGTTATTTGAT	240756
rs30871921	snp	A/G	0.493827	0.0552116	utr-variant-3-prime	Klhl12	GRCm38.p3	1:134490151	TAAATTGGAAGGCTG[A/G]AAAGGACATGTTATT	240756
rs30871922	snp	A/C	0.124444	0.216185	utr-variant-3-prime	Klhl12	Mm_Celera	1:134489972	AGGTAGCTCAAGCCA[A/C]CACAGTTCCTTGCTG	240756
rs30871923	snp	C/T	0.32	0.24	utr-variant-3-prime	Klhl12	GRCm38.p3	1:134489941	TCAGAAGCAAAAATA[C/T]CTTTTCTAAATACAG	240756
rs30872224	snp	C/T	0.444444	0.157135	intron-variant	Klhl12	GRCm38.p3	1:134471606	TCACAGTCAACCGTT[C/T]AGATGAGGCCTTGGG	240756
rs30872225	snp	C/T	0.32	0.24	intron-variant	Klhl12	GRCm38.p3	1:134471468	GAAGGCAGAGTCTGG[C/T]CTACAGGGACTGGAC	240756

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