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
rs13264	snp	C/T	0	0	intron-variant	AMBRA1	GRCh38.p7	11:46428743	TGTGCCACCTGGTGC[C/T]GACAAGAAAGCCGAG	55626
rs14196	snp	A/G			intron-variant	AMBRA1	GRCh38.p7	11:46428777	GGGAAGCTGACAGAG[A/G]TACCTACAGACGGAG	55626
rs713120	snp	A/G	0	0	intron-variant	AMBRA1	GRCh38.p7	11:46529050	GGAGTAGAAAATTGT[A/G]ATAATAAAGGAATCA	55626
rs756343	snp	G/T	0.101301	0.200969	intron-variant	AMBRA1	GRCh38.p7	11:46528726	TTAATAATTTTAAAA[G/T]TGTACAGTACACATT	55626
rs870242	snp	C/T	0	0	intron-variant	AMBRA1	GRCh38.p7	11:46496432	AGAAAAGAAGCATCA[C/T]GGGTCAAATCTAATT	55626
rs901997	snp	G/T	0.014507	0.0839229	intron-variant	AMBRA1	GRCh38.p7	11:46505354	ATTCAGTTTACTGTA[G/T]AGGGAGGTGGGCAGG	55626
rs901999	snp	A/C	0.0418186	0.138422	intron-variant	AMBRA1	GRCh38.p7	11:46404874	GGGCTGCATGCTAAC[A/C]AAGAAAACAGCAGAG	55626
rs931402	snp	A/G/T	0.000399281	0.0141238	intron-variant	AMBRA1	GRCh38.p7	11:46432043	tatttttatttattt[A/G/T]tttttttttGAGATT	55626
rs967754	snp	C/T	0.0298908	0.118541	intron-variant	AMBRA1	GRCh38.p7	11:46415239	TTCATGTCTTTTGAG[C/T]GGTCTACAGATGAGT	55626
rs1052395	snp	A/C			intron-variant	AMBRA1	GRCh38.p7	11:46428752	ACGGAGTGCTGTGCC[A/C]CCTGGTGCCGACAAG	55626
rs1140566	snp	C/T	0	0	intron-variant	AMBRA1	GRCh38.p7	11:46428769	GCACAGCACTCCGTC[C/T]GTAGGTATCTCTGTC	55626
rs1140567	snp	C/T			intron-variant	AMBRA1	GRCh38.p7	11:46428771	ACAGCACTCCGTCTG[C/T]AGGTATCTCTGTCAG	55626
rs1466634	snp	A/C	0.0170251	0.090679	utr-variant-3-prime, nc-transcript-variant	AMBRA1	GRCh38.p7	11:46396508	TTCTGTTTGTAACTC[A/C]TCATAGAAACATTGT	55626
rs1466635	snp	C/T	0.110872	0.20771	downstream-variant-500B	AMBRA1	GRCh38.p7	11:46396265	CCCCTCTGACCCCTT[C/T]GCCAGAGCTGGTCAG	55626
rs1472000	snp	G/T	0.0109286	0.0731087	intron-variant	AMBRA1	GRCh38.p7	11:46444276	TCAAGGAGGTTCTTA[G/T]GGGGTAGGTATTATA	55626
rs1472001	snp	A/G	0.289165	0.246913	intron-variant	AMBRA1	GRCh38.p7	11:46463135	GCCCCATGGCACTTT[A/G]TTTCTCTCTTATTCT	55626
rs1489189	snp	A/G	0.0174175	0.0916809	intron-variant	AMBRA1	GRCh38.p7	11:46509714	TGTATACACTAATAC[A/G]TATACTAAAATATGT	55626
rs1489190	snp	C/T	0.0314385	0.121371	intron-variant	AMBRA1	GRCh38.p7	11:46509900	GATTAAGAACAGAAA[C/T]AGGAATAGTTATATC	55626
rs1489191	snp	A/G	0	0	intron-variant	AMBRA1	GRCh38.p7	11:46509933	AATGGTACAAAAAGT[A/G]TTGGCAACTATCTTG	55626
rs1489192	snp	A/G	0.312348	0.242101	intron-variant	AMBRA1	GRCh38.p7	11:46487794	GGGTTTTTGTCTGCC[A/G]TTTTACTGTTTGTTT	55626
rs1489193	snp	C/T	0.0170251	0.090679	intron-variant	AMBRA1	GRCh38.p7	11:46463649	AAGATACCCACTCAA[C/T]CGTCAGAATGGCACT	55626
rs1812657	snp	C/G	0.0298908	0.118541	intron-variant	AMBRA1	GRCh38.p7	11:46427738	AACAGGCCGGGAGCG[C/G]TGGCTCATGCCTGTA	55626
rs1873129	snp	A/G	0.0298908	0.118541	intron-variant	AMBRA1	GRCh38.p7	11:46479865	cttgtttaagccact[A/G]agtttctgcttgttg	55626
rs1873130	snp	A/G	0.138886	0.22395	intron-variant	AMBRA1	GRCh38.p7	11:46535971	ACATCAGAGGTCACC[A/G]GAGCTCAAGTTTTGG	55626
rs2014722	snp	C/G	0.0107246	0.0724382	intron-variant	AMBRA1	GRCh38.p7	11:46496896	tcgaacttctaactt[C/G]aagtgatctgcccgc	55626
rs2029378	snp	A/G	0.0298908	0.118541	intron-variant	AMBRA1	GRCh38.p7	11:46433248	CTTGCAGGCCTCTGG[A/G]GAATGCAGCACATAT	55626
rs2046766	snp	A/C	0.0298908	0.118541	intron-variant	AMBRA1	GRCh38.p7	11:46425914	CACTTTGGGAGGCTG[A/C]GGTGGGCAGATCACA	55626
rs2046767	snp	A/G	0.0298908	0.118541	intron-variant	AMBRA1	GRCh38.p7	11:46429962	AGAGTAGCATATCCA[A/G]TCTGGAGGAATCGCA	55626
rs2171667	snp	C/G	0.329691	0.24138	intron-variant	AMBRA1	GRCh38.p7	11:46445542	CCTTTTAATAAAGTC[C/G]TTCAGGTATCTTACC	55626
rs2171668	snp	G/T	0.322483	0.239262	intron-variant	AMBRA1	GRCh38.p7	11:46445278	GGATGTCTTGTTTTG[G/T]GGGTATTCATTTATC	55626
rs2291487	snp	C/T	0.201727	0.245295	intron-variant	AMBRA1	GRCh38.p7	11:46434794	CTCACCTAGCAATGA[C/T]CATGCCAAGGCACCA	55626
rs2864071	snp	A/G	0.030278	0.119257	intron-variant	AMBRA1	GRCh38.p7	11:46405230	aggagtctcccctaa[A/G]ccccacaggctgggc	55626
rs2864072	snp	G/T	0.312593	0.242037	intron-variant	AMBRA1	GRCh38.p7	11:46447309	GACCTCAAGTGATCC[G/T]CCTGCCTTGGCCTCA	55626
rs2864076	snp	A/G	0.319136	0.24025	intron-variant	AMBRA1	GRCh38.p7	11:46438488	CTGCTAATTGCTCCC[A/G]TGGCCTCATCTGGCC	55626
rs2864834	snp	C/T	0.030278	0.119257	intron-variant	AMBRA1	GRCh38.p7	11:46428592	CTTCTTCTTCTTCTT[C/T]TTTTTTTTTTAAGGT	55626
rs2864835	snp	C/T	0	0	intron-variant	AMBRA1	GRCh38.p7	11:46429099	CCACCATGACTCCCT[C/T]CTTAAAAAGGAGTTC	55626
rs2864836	snp	C/T	0.00757384	0.0610701	synonymous-codon, nc-transcript-variant	AMBRA1	GRCh38.p7	11:46542541	ATGGCGAATGCTGCC[C/T]GAGTTGTTTTGGCTG	55626
rs2902858	snp	C/T	0.322959	0.239117	intron-variant	AMBRA1	GRCh38.p7	11:46502463	GAAGTAGATAATACC[C/T]TATCCCTCTCTGACG	55626
rs3071087	in-del	-/AT			intron-variant	AMBRA1	GRCh38.p7	11:46528754	taagagggtaaatct[-/AT]gttatgttttctatc	55626
rs3178098	snp	A/C			intron-variant	AMBRA1	GRCh38.p7	11:46428607	ACTTATAGCCAAAAA[A/C]CCTTAAaaaaaaaag	55626
rs3179874	snp	A/T			intron-variant	AMBRA1	GRCh38.p7	11:46428591	CCTTAAaaaaaaaag[A/T]agaagaagaagaaga	55626
rs3180415	snp	A/C			intron-variant	AMBRA1	GRCh38.p7	11:46428613	GAATAAACTTATAGC[A/C]AAAAAACCTTAAaaa	55626
rs3206777	snp	C/T	0	0	intron-variant	AMBRA1	GRCh38.p7	11:46514038	TCTCTGAGACCATTT[C/T]CTTTGAAACATGTTC	55626
rs3210531	snp	C/G			intron-variant	AMBRA1	GRCh38.p7	11:46428800	GCGACCTGCGAGACT[C/G]ACAAGAGGGGAAGCT	55626
rs3740973	snp	A/G	0.48995	0.0701706	intron-variant	AMBRA1	GRCh38.p7	11:46400687	AGAGACGGTTTCGCC[A/G]TGTTGCCCAGGCTGG	55626
rs3802887	snp	C/G			intron-variant	AMBRA1	GRCh38.p7	11:46429849	TCAGCTCAGCAGTCT[C/G]TAAAAGCTTAACCTA	55626
rs3802888	snp	A/G	0.375399	0.216275	intron-variant	AMBRA1	GRCh38.p7	11:46494352	GCTCACTAATTAGGC[A/G]GCACATTAATAAAAC	55626
rs3802889	snp	C/G/T	0.00159617	0.0282053	intron-variant	AMBRA1	GRCh38.p7	11:46512964	CTTCTACAAGCTAAG[C/G/T]AGGTAGAGACACAAA	55626
rs3802890	snp	A/G	0.489837	0.0705577	intron-variant	AMBRA1	GRCh38.p7	11:46512996	AAATGAAGAGCTGCA[A/G]AACTCCCACACTGGA	55626
rs3839953	in-del	-/A	0.0821764	0.185298	intron-variant, frameshift-variant	AMBRA1	GRCh38.p7	11:46431083	ACGTAAGGGGCAACC[-/A]AGACCTGGAAAACCA	55626
rs3897850	snp	G/T	0	0	intron-variant	AMBRA1	GRCh38.p7	11:46492230	CTCTGTCAGACACCA[G/T]GACTTCATAGGCTCT	55626
rs3961051	snp	A/T			intron-variant	AMBRA1	GRCh38.p7	11:46428994	CGTAGCCTCGGGACT[A/T]GAGAGACTGCATGGC	55626
rs3975806	snp	C/T			intron-variant	AMBRA1	GRCh38.p7	11:46429010	GAGAGACTGCATGGC[C/T]TTCATGACATGAAGG	55626
rs3976777	in-del	-/GTT			intron-variant	AMBRA1	GRCh38.p7	11:46487341	aacaagtaaattgtt[-/GTT]nnaaccaaaaataaa	55626
rs4376875	snp	C/T	0.0298908	0.118541	intron-variant	AMBRA1	GRCh38.p7	11:46429645	TCTTTCTGGTTTCAT[C/T]AGTAATTTTGTATTT	55626
rs4433539	snp	C/T	0.0298908	0.118541	intron-variant	AMBRA1	GRCh38.p7	11:46420230	TCCAAATGTAAGGAA[C/T]TCGTTAAGGCTCCTT	55626
rs4508179	snp	A/G	0.0298908	0.118541	intron-variant	AMBRA1	GRCh38.p7	11:46403924	AATCTGTGTGGCTGC[A/G]TGTGGCGGCTCACGC	55626
rs4550197	snp	C/T	0.0314385	0.121371	intron-variant	AMBRA1	GRCh38.p7	11:46424454	CTTTCCAAAGGCCAC[C/T]CCTGGCCATTAGGAT	55626
rs4568980	snp	G/T	0.0926964	0.194308	intron-variant	AMBRA1	GRCh38.p7	11:46517933	ATTCGTATATATATA[G/T]AGAGAGAGAGAACAA	55626
rs4752802	snp	C/G	0	0	intron-variant	AMBRA1	GRCh38.p7	11:46577840	ctataatcccagcta[C/G]tcaggaggctgaggc	55626
rs4995987	snp	A/G			intron-variant, upstream-variant-2KB, downstream-variant-500B	AMBRA1, MIR3160-1, MIR3160-2	GRCh38.p7	11:46452262	TTCATTTGTTTACCA[A/G]CTCACTGTGTATCTT	55626
rs6485680	snp	A/T	0.138207	0.223612	intron-variant	AMBRA1	GRCh38.p7	11:46421433	CCTCCTGGATCCTGA[A/T]AAGCACTTGCTTGCT	55626
rs6485681	snp	C/T	0.0298908	0.118541	intron-variant	AMBRA1	GRCh38.p7	11:46421699	CTCACTGAAGGGAAA[C/T]ACCTCTCACAATTAG	55626
rs6485682	snp	A/C	0.3742	0.216966	intron-variant	AMBRA1	GRCh38.p7	11:46424714	gcatggtggcacata[A/C]ctctaatcctagcta	55626
rs7101862	snp	A/G	0	0	intron-variant	AMBRA1	GRCh38.p7	11:46466502	AGCATGTGGAAAGGA[A/G]AATGGTTCAGGATAG	55626
rs7104073	snp	C/G	0.375399	0.216275	intron-variant	AMBRA1	GRCh38.p7	11:46574469	taaatgtcttctttt[C/G]agaagtgtctgttca	55626
rs7106740	snp	A/T	0.0174175	0.0916809	intron-variant	AMBRA1	GRCh38.p7	11:46489947	ccaggtcagcctctc[A/T]cagtgatattgggca	55626
rs7109222	snp	C/T	0	0	intron-variant	AMBRA1	GRCh38.p7	11:46529567	GAGCTAATGCAATGG[C/T]CAAGTACACAAAATT	55626
rs7110413	snp	A/G	0.0410537	0.137264	intron-variant	AMBRA1	GRCh38.p7	11:46563516	aggcatgagccacAC[A/G]GCACCCTGATGAGAA	55626
rs7112229	snp	C/T	0.282895	0.247826	intron-variant	AMBRA1	GRCh38.p7	11:46491699	GGGAGTCTAGAGTTC[C/T]TTCTCCTAATGGCAT	55626
rs7117179	snp	A/G	0	0	intron-variant	AMBRA1	GRCh38.p7	11:46570347	AGTCTCCTCCATGGA[A/G]CTATCCTGTGGGCCC	55626
rs7117944	snp	A/C	0.0418186	0.138422	intron-variant	AMBRA1	GRCh38.p7	11:46475878	AGCAGGCAGCTTCAA[A/C]TAAAGGATATACTAA	55626
rs7119921	snp	A/T	0.130694	0.219696	intron-variant	AMBRA1	GRCh38.p7	11:46428133	GGTATAAAGGGATAG[A/T]CCACTACTGACCAGC	55626
rs7120080	snp	C/G	0	0	intron-variant	AMBRA1	GRCh38.p7	11:46516003	TACAATCCTAAAAGT[C/G]TATTTCCCACCTTAA	55626
rs7121994	snp	A/G			intron-variant	AMBRA1	GRCh38.p7	11:46571555	tggcacatacctgta[A/G]tcccagctactcagg	55626
rs7123865	snp	C/T	0	0	intron-variant	AMBRA1	GRCh38.p7	11:46432856	TGAGCACCTATGGGA[C/T]GTGGGACGTTCACTC	55626
rs7124013	snp	A/G	0.000399281	0.0141238	intron-variant	AMBRA1	GRCh38.p7	11:46524030	tgcaccaccatgccc[A/G]gctaattttgtattt	55626
rs7127529	snp	A/C	0.323908	0.238825	intron-variant	AMBRA1	GRCh38.p7	11:46560522	CCGGAAATAGAAAGC[A/C]ATAAGACCCAAATTT	55626
rs7129348	snp	A/T	0.105214	0.203807	intron-variant	AMBRA1	GRCh38.p7	11:46488500	aagggaaaaatacac[A/T]attcaataataatag	55626
rs7130028	snp	C/T	0.499897	0.00718776	intron-variant	AMBRA1	GRCh38.p7	11:46556973	gaaaccctgtctcta[C/T]taaaaatacaaaatt	55626
rs7130141	snp	C/T	0.375598	0.21616	intron-variant	AMBRA1	GRCh38.p7	11:46478324	TTATAAATGATGCCA[C/T]GGGTACAGGTTCACT	55626
rs7481312	snp	C/T	0.31357	0.241783	intron-variant	AMBRA1	GRCh38.p7	11:46575124	AAGTACCAGTGGTAT[C/T]AGTAACTCCCtctta	55626
rs7482883	snp	A/G	0	0	intron-variant	AMBRA1	GRCh38.p7	11:46577032	ATCACATACTCTGGA[A/G]AAGCTGCAGATGTTG	55626
rs7483199	snp	C/G			intron-variant	AMBRA1	GRCh38.p7	11:46484645	ccaccacctatactt[C/G]tttggcttttttttt	55626
rs7484125	snp	C/T	0.489376	0.0721049	intron-variant	AMBRA1	GRCh38.p7	11:46566717	taacagtaagaaaag[C/T]atgacagtgaaaaag	55626
rs7924437	snp	G/T	0.0298908	0.118541	intron-variant	AMBRA1	GRCh38.p7	11:46406058	Ctttatttatttatt[G/T]tattattatttttga	55626
rs7924695	snp	A/G	0.0298908	0.118541	intron-variant	AMBRA1	GRCh38.p7	11:46406228	ccggctaatttttgt[A/G]tttttagtagagaca	55626
rs7925678	snp	A/G	0.489893	0.0703642	intron-variant	AMBRA1	GRCh38.p7	11:46549309	GTGTTATCCACTGTG[A/G]CATTGTTTCTTTAGC	55626
rs7928869	snp	G/T	0.0298908	0.118541	intron-variant	AMBRA1	GRCh38.p7	11:46407292	CTCTCGCTGTCAGGG[G/T]TTACTGGGAGCTCTG	55626
rs7930103	snp	C/T	0.289424	0.246872	intron-variant	AMBRA1	GRCh38.p7	11:46462704	ATGTTTACTAAAATC[C/T]CCTTCATCCCTCATC	55626
rs7930857	snp	A/G	0.0887219	0.191022	intron-variant	AMBRA1	GRCh38.p7	11:46425889	tggtgtctcacgcct[A/G]taatcccagcacttt	55626
rs7932866	snp	A/G	0.271972	0.249033	intron-variant	AMBRA1	GRCh38.p7	11:46526544	taaaaaaaaaattaa[A/G]attaaaaaaaaaaaa	55626
rs7942262	snp	C/T			intron-variant	AMBRA1	GRCh38.p7	11:46523611	TTCTTTTTATTAGCA[C/T]TAATGGCTATAATCT	55626
rs7942614	snp	C/T	0.0916144	0.193427	intron-variant	AMBRA1	GRCh38.p7	11:46428883	GTAGGATGGCAGGCA[C/T]AATCTCTGGGGGCAG	55626
rs7942788	snp	C/T	0.0170251	0.090679	intron-variant	AMBRA1	GRCh38.p7	11:46423050	AGGTTTTAGTGAGGG[C/T]TACTAGAAGAGAATC	55626
rs7946071	snp	A/G	0.0422008	0.138995	intron-variant	AMBRA1	GRCh38.p7	11:46429198	CTCCCCCTCTCCCTC[A/G]GACAATCTTCGCCTA	55626
rs7946705	snp	A/G	0.274393	0.248807	intron-variant	AMBRA1	GRCh38.p7	11:46399608	gacttcaggcgatcc[A/G]cccacctaggcctcc	55626
rs7946801	snp	A/G	0.039522	0.134904	intron-variant	AMBRA1	GRCh38.p7	11:46547722	ATACAGTACTTCAGA[A/G]AGACTTTAGGGACTG	55626
rs7949282	snp	A/C	0.490453	0.0684267	intron-variant	AMBRA1	GRCh38.p7	11:46500756	GCTATACCCATCACC[A/C]ATATCAATTCCTCTC	55626
rs7949371	snp	C/T	0.490453	0.0684267	intron-variant	AMBRA1	GRCh38.p7	11:46500754	TCGCTATACCCATCA[C/T]CAATATCAATTCCTC	55626

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