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
rs1995	snp	C/T	0.258565	0.249853	utr-variant-3-prime, intron-variant	N4BP2	GRCh38.p7	4:40158088	TTTTCTGATATACTG[C/T]CTGAAAATTTTATAA	55728
rs793993	snp	G/T	0.288646	0.246995	intron-variant	N4BP2	GRCh38.p7	4:40111808	gccaacatggtgaaa[G/T]cccatctctactaaa	55728
rs793994	snp	A/G	0.288646	0.246995	intron-variant	N4BP2	GRCh38.p7	4:40111432	ttgggaggctgagac[A/G]gcagaatcacttgaa	55728
rs793995	snp	A/T	0.448963	0.151372	intron-variant	N4BP2	GRCh38.p7	4:40111068	AACAAATGGACAAAT[A/T]TACACACACACAATG	55728
rs793996	snp	C/T	0.184521	0.241273	intron-variant	N4BP2	GRCh38.p7	4:40110992	GGGATTTTCTTACCT[C/T]TCTTCCAAAGGAATT	55728
rs793997	snp	A/T	0.160609	0.233472	intron-variant	N4BP2	GRCh38.p7	4:40127094	agaccagcctgggca[A/T]catggcaaaactgtc	55728
rs793998	snp	A/G	0.290977	0.246619	intron-variant	N4BP2	GRCh38.p7	4:40125495	TAAATAGAGGAAGTT[A/G]TAGCCAGCTGGAAGT	55728
rs793999	snp	A/C	0.168135	0.236216	intron-variant	N4BP2	GRCh38.p7	4:40097677	TTCTATTTTATTCAT[A/C]ATTTATTAATCATCT	55728
rs794000	snp	A/G	0.0349115	0.127424	intron-variant	N4BP2	GRCh38.p7	4:40104534	CTAACTGACTTAATA[A/G]CAACAACAACATAAA	55728
rs794001	snp	A/G	0.306922	0.243434	missense, nc-transcript-variant	N4BP2	GRCh38.p7	4:40119942	TACAGCCCAAGAGAC[A/G]ATGAAGATATTATCT	55728
rs794002	snp	C/T	0.325563	0.238307	intron-variant	N4BP2	GRCh38.p7	4:40142453	TTCTTTAACCACTCT[C/T]GGGAGATGTTGAAGA	55728
rs794003	snp	A/C	0.324382	0.238678	intron-variant	N4BP2	GRCh38.p7	4:40142179	ctgaagtgaagttac[A/C]aaggttacacGCTGc	55728
rs794004	snp	C/T	0.290201	0.246747	intron-variant	N4BP2	GRCh38.p7	4:40142129	ctccccctccccctc[C/T]ccctatggtctccct	55728
rs794005	snp	C/G	0.255782	0.249933	intron-variant	N4BP2	GRCh38.p7	4:40141324	agccgccccgtctga[C/G]aagtgaggagcgtca	55728
rs794006	snp	C/T	0.292523	0.246357	intron-variant	N4BP2	GRCh38.p7	4:40141121	ctgcccggccaccac[C/T]ccatctgggaggtgt	55728
rs794007	snp	A/G	0.299411	0.245069	intron-variant	N4BP2	GRCh38.p7	4:40140915	ggatcctgttgatct[A/G]tgaccttacccccaa	55728
rs794008	snp	A/G	0.289942	0.246789	intron-variant	N4BP2	GRCh38.p7	4:40138718	cagcaataaatcctt[A/G]taactatggtcaatt	55728
rs794009	snp	A/C	0.295854	0.245759	intron-variant	N4BP2	GRCh38.p7	4:40138099	gtattctgccactgg[A/C]atttttgcagccttc	55728
rs794010	snp	C/T	0.163892	0.234703	intron-variant	N4BP2	GRCh38.p7	4:40137977	acctgtctgggagca[C/T]gcctttcatttggaa	55728
rs794011	snp	A/C	0.161267	0.233723	intron-variant	N4BP2	GRCh38.p7	4:40137794	aacctgcttaccctg[A/C]cttacccattccttc	55728
rs794012	snp	A/G	0.161596	0.233848	intron-variant	N4BP2	GRCh38.p7	4:40136531	ggtgtggtgacgcgc[A/G]cctgtaatcccagct	55728
rs794018	snp	A/G	0.36606	0.221428	intron-variant	N4BP2	GRCh38.p7	4:40167804	GTCTTTATTTAACAC[A/G]TATAGTACACATTTT	55728
rs794019	snp	C/G	0.44546	0.155869	intron-variant	N4BP2	GRCh38.p7	4:40161105	TTATGACTTCGGGCT[C/G]TTATTCTGTGAGGGC	55728
rs794020	snp	A/G	0.0267878	0.112589	intron-variant	N4BP2	GRCh38.p7	4:40160910	TTATGGAGTGTCTTA[A/G]TCTTTAAGTCTGCTG	55728
rs794021	snp	A/T	0.411578	0.190768	intron-variant	N4BP2	GRCh38.p7	4:40069721	AGGGTCTCGCTTTGC[A/T]GCCCACACTGGTCTC	55728
rs794022	snp	C/G	0.193653	0.243567	intron-variant	N4BP2	GRCh38.p7	4:40069248	gtttcaccatgttgg[C/G]caggctggtcttgaa	55728
rs794023	snp	C/T	0.202035	0.245356	intron-variant	N4BP2	GRCh38.p7	4:40066414	agagaattgcttgaa[C/T]ctgggaggcagaggc	55728
rs794024	snp	C/T	0.190519	0.242821	intron-variant	N4BP2	GRCh38.p7	4:40066405	cttgaacctgggagg[C/T]agaggctgcaatgag	55728
rs794025	snp	A/G	0.193653	0.243567	intron-variant	N4BP2	GRCh38.p7	4:40066353	tcagcctgagcaaca[A/G]agtgagacactgtct	55728
rs794026	snp	A/G	0.192715	0.243348	intron-variant	N4BP2	GRCh38.p7	4:40065999	AGGTTGCAGTGAGCC[A/G]AGATCACGCCACTGC	55728
rs794027	snp	A/G	0.182614	0.240747	intron-variant	N4BP2	GRCh38.p7	4:40064377	TGAGGCAGGAGAATC[A/G]CTTGAACCCAAGAGG	55728
rs794028	snp	A/G	0.19459	0.243782	intron-variant	N4BP2	GRCh38.p7	4:40062060	accaaaaaaTAAAGC[A/G]GTAAAAACAAAACAA	55728
rs794029	snp	A/G	0.192088	0.2432	intron-variant	N4BP2	GRCh38.p7	4:40061521	aaaacttagctgggc[A/G]tggtggtgcacatct	55728
rs794030	snp	A/G	0	0	intron-variant	N4BP2	GRCh38.p7	4:40060694	gatcccttgagccca[A/G]gaattcaaggctaca	55728
rs794031	snp	A/G	0.247337	0.249986	intron-variant	N4BP2	GRCh38.p7	4:40059591	AGGCCAAAGCGGGCG[A/G]ATCACTTGAGGCCAG	55728
rs807787	snp	C/T	0.157311	0.232183	intron-variant	N4BP2	GRCh38.p7	4:40150036	ACAGTAACTACAGAC[C/T]ACCACAGGTGGCAGC	55728
rs809913	snp	A/C	0.497855	0.0326773	intron-variant	N4BP2	GRCh38.p7	4:40111262	aaatcaaactatagt[A/C]ttgagtttagttaat	55728
rs809914	snp	A/G	0.244776	0.249945	intron-variant	N4BP2	GRCh38.p7	4:40160050	gatggatcacctaag[A/G]tcaggaattcgagac	55728
rs809915	snp	C/T	0.192401	0.243274	intron-variant	N4BP2	GRCh38.p7	4:40060338	agaattgcttgaacc[C/T]gggaggcagaggttg	55728
rs813230	snp	G/T	0.425586	0.17796	intron-variant, upstream-variant-2KB	N4BP2	GRCh38.p7	4:40095995	gaggttGGAATATGG[G/T]TGAAAGATGACAGGT	55728
rs813809	snp	C/T			intron-variant	N4BP2	GRCh38.p7	4:40174775	ccactgcactccagt[C/T]tgggcgacagagtga	55728
rs813810	snp	A/G			intron-variant	N4BP2	GRCh38.p7	4:40175106	actcactgcagccta[A/G]aattcctggcctcaa	55728
rs907356	snp	C/T	0.203882	0.245709	intron-variant, upstream-variant-2KB	N4BP2, LOC344967	GRCh38.p7	4:40057256	GGCTGAGCGCCAGGG[C/T]CCGCCTCTCGCCGAC	55728
rs937967	snp	A/C	0.14665	0.227637	intron-variant, nc-transcript-variant	N4BP2, LOC344967	GRCh38.p7	4:40057142	GGGGTTCATTCGCCG[A/C]GCCGCCCGCCGCTGC	55728
rs937968	snp	A/G	0	0	intron-variant	N4BP2	GRCh38.p7	4:40125051	ATGTGGAGGAACTCA[A/G]GCACAAAAGGAGGAT	55728
rs971010	snp	A/G	0	0	intron-variant	N4BP2	GRCh38.p7	4:40091506	ttttaatgcgtgaaa[A/G]aattgtatcaatcaa	55728
rs1004294	snp	C/T	0.0498117	0.149749	intron-variant	N4BP2	GRCh38.p7	4:40061003	aaatttaaattgaga[C/T]ggggtgttgccatat	55728
rs1008086	snp	C/T	0.152334	0.230133	intron-variant	N4BP2	GRCh38.p7	4:40145137	ACTTAATTGATATTT[C/T]TTGGATTTCAATTTT	55728
rs1087313	snp	C/T	0.191147	0.242974	intron-variant	N4BP2	GRCh38.p7	4:40067817	cagctactcgggagg[C/T]tgagacaggagaatc	55728
rs1091048	snp	A/G	0	0	intron-variant	N4BP2	GRCh38.p7	4:40088684	tttgtatttttacta[A/G]aaacggggtttctcc	55728
rs1128372	snp	C/T	0.320763	0.239776	synonymous-codon, nc-transcript-variant	N4BP2	GRCh38.p7	4:40117881	CAGGCGTAACATTCA[C/T]GGGGTAAGCAAAGAA	55728
rs1128374	snp	C/T	3.30006e-05	0.00406192	missense, nc-transcript-variant	N4BP2	GRCh38.p7	4:40117927	TTGGAACATTATCAA[C/T]GTTTTGTTTCAGTGC	55728
rs1396952	snp	G/T	0.318415	0.240457	upstream-variant-2KB, intron-variant	N4BP2, LOC344967	GRCh38.p7	4:40055239	TCAAAAACAAAAAAT[G/T]GTAATAACCCAGAAT	55728
rs1397933	snp	G/T	0.263809	0.249618	utr-variant-3-prime, intron-variant	N4BP2	GRCh38.p7	4:40185917	GTTTTCCTCTAATGA[G/T]CCTCAAGCATTTCCC	55728
rs1397934	snp	A/G	0.257454	0.249889	utr-variant-3-prime, intron-variant	N4BP2	GRCh38.p7	4:40185976	CTGAATTAATTACCC[A/G]GAAACCTCACTTTTT	55728
rs1509813	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	N4BP2, LOC344967	GRCh38.p7	4:40057915	GCATGGCGAGAATGT[C/G]TACAAACCTGTCCGT	55728
rs1533063	snp	C/T	0.288646	0.246995	intron-variant	N4BP2	GRCh38.p7	4:40114842	GAAACGTTGCTATAA[C/T]GGAAAAATTCCAACT	55728
rs1533064	snp	A/G	0.449853	0.150196	intron-variant	N4BP2	GRCh38.p7	4:40114747	ttagataaacctaga[A/G]aagaagaaaagagga	55728
rs1553773	snp	C/G	0.0498117	0.149749	intron-variant	N4BP2	GRCh38.p7	4:40060753	gagccaggcacagcg[C/G]tatgtgcctatactc	55728
rs1623354	snp	C/T	0.2462	0.249971	downstream-variant-500B, intron-variant	N4BP2	GRCh38.p7	4:40158391	ACAGAAAACGTAAAC[C/T]AGAAGAAAAGTTTTG	55728
rs1623513	snp	A/G	0.0352966	0.128072	downstream-variant-500B, intron-variant	N4BP2	GRCh38.p7	4:40158320	TACAAAGTTAGACAT[A/G]AAAATATTTTAAAAT	55728
rs1624604	snp	A/G	0.192088	0.2432	intron-variant, upstream-variant-2KB	N4BP2, LOC344967	GRCh38.p7	4:40058977	AAAAATTAGCCGGGC[A/G]TAGTGGCTTTCGCCT	55728
rs1625495	snp	C/T	0.191775	0.243125	intron-variant, upstream-variant-2KB	N4BP2, LOC344967	GRCh38.p7	4:40058855	CCAGCCTTGGCGATA[C/T]GGCCAGACCTTGTCT	55728
rs1704153	snp	C/T	0.383824	0.211166	intron-variant	N4BP2	GRCh38.p7	4:40098964	GGGTTTCTAATCTAC[C/T]GAGTTGTGCTGTAGT	55728
rs1704154	snp	C/T	0.497881	0.0324789	intron-variant	N4BP2	GRCh38.p7	4:40107130	tttgagacagggtct[C/T]gctgtgttgcacagg	55728
rs1704155	snp	A/G	0.127599	0.217986	upstream-variant-2KB, intron-variant, utr-variant-5-prime, nc-transcript-variant	N4BP2, LOC344967	GRCh38.p7	4:40056289	AAGGTCGGCCTCGCG[A/G]GGTGAGGGGAGAAAG	55728
rs1704156	snp	A/G	0.204803	0.245881	upstream-variant-2KB, intron-variant	N4BP2, LOC344967	GRCh38.p7	4:40056079	TCGGAGCCCCACGGG[A/G]AGACAAAGGGGTAGG	55728
rs1704157	snp	A/G	0.315758	0.241197	upstream-variant-2KB, intron-variant	N4BP2, LOC344967	GRCh38.p7	4:40055669	GTCCCCTCCCTTTGC[A/G]GTTACTTTTCATTCC	55728
rs1704158	snp	A/G	0.202035	0.245356	intron-variant	N4BP2	GRCh38.p7	4:40071607	tgcactccagcctgg[A/G]caacaagagcaaaac	55728
rs1704160	snp	A/G	0.215747	0.247642	intron-variant	N4BP2	GRCh38.p7	4:40144072	GGCTCAAGAGCCACC[A/G]AGAGGCAGCTGGTGC	55728
rs1706022	snp	A/C	0.154993	0.231244	intron-variant	N4BP2	GRCh38.p7	4:40159579	AACCATCTTTAAGAC[A/C]ACTTGGCACTTGCCT	55728
rs1706023	snp	C/T	0.388587	0.208071	intron-variant	N4BP2	GRCh38.p7	4:40073122	aggaacaacagaacc[C/T]aaaactaattaccat	55728
rs1706024	snp	G/T	0.335152	0.279336	upstream-variant-2KB, intron-variant, missense, nc-transcript-variant	N4BP2, LOC344967	GRCh38.p7	4:40056443	GTGTCGGGTTCTGCT[G/T]GGGGGGAAGGCGGGA	55728
rs1706025	snp	C/T	0.145305	0.227022	upstream-variant-2KB, intron-variant	N4BP2, LOC344967	GRCh38.p7	4:40056038	GGGGTGGAGGGAGGC[C/T]GCCCAGCCCCATCGG	55728
rs1706026	snp	A/G	0.0111196	0.0737302	intron-variant	N4BP2	GRCh38.p7	4:40117398	TTGAATTCAACCCAA[A/G]ACAGGAAAGTTGCAA	55728
rs1706027	snp	A/G	0.16976	0.236773	intron-variant, upstream-variant-2KB	N4BP2	GRCh38.p7	4:40079125	agaccagcctggcca[A/G]cacggtaaaacccca	55728
rs1706028	snp	C/G	0.223522	0.248594	intron-variant	N4BP2	GRCh38.p7	4:40099056	AATATTTTTTTCTTT[C/G]TTTTGGCTTTTTTTT	55728
rs1706029	snp	A/G	0	0	intron-variant	N4BP2	GRCh38.p7	4:40126752	aaataaaaaTACCCA[A/G]gcctggtagtccctg	55728
rs1706030	snp	A/C			intron-variant	N4BP2	GRCh38.p7	4:40126749	taaaaaTACCCAAGC[A/C]TGgtagtccctgtta	55728
rs1706032	snp	A/G	0.256061	0.249927	intron-variant	N4BP2	GRCh38.p7	4:40148264	acagggtttcgctgt[A/G]ttggccaggctgctc	55728
rs1706034	snp	A/G	0.450483	0.149354	intron-variant	N4BP2	GRCh38.p7	4:40119277	AGGAAGGCATCCTGC[A/G]AGAGTTGGGACTTCG	55728
rs1714383	snp	A/G	0.255503	0.249939	intron-variant	N4BP2	GRCh38.p7	4:40150292	AAATCCCTATAAAAT[A/G]GTAGTCAGTTCTAAA	55728
rs1714384	snp	C/T	0.155987	0.23165	intron-variant	N4BP2	GRCh38.p7	4:40150287	CCTATAAAATGGTAG[C/T]CAGTTCTAAAGGTTT	55728
rs1714385	snp	C/G	0.155987	0.23165	intron-variant	N4BP2	GRCh38.p7	4:40148416	cctctgatgccgagc[C/G]gaagctggactgtac	55728
rs1714386	snp	C/T	0.155987	0.23165	intron-variant	N4BP2	GRCh38.p7	4:40148322	ctgcgattgcaggcg[C/T]gcgccgccatgcgtg	55728
rs1714387	snp	C/T	0.163892	0.234703	intron-variant	N4BP2	GRCh38.p7	4:40143865	AAATTATCTTTCATA[C/T]ATCCTACTGGTCTGT	55728
rs1812396	snp	C/T	0.201727	0.245295	intron-variant	N4BP2	GRCh38.p7	4:40109497	cttaggcagatggat[C/T]acctgaagtcaagag	55728
rs1876874	snp	G/T	0.268724	0.249298	intron-variant	N4BP2	GRCh38.p7	4:40117779	CGTATCTATTAGAAA[G/T]ATATTATTGTTTTCC	55728
rs1985721	snp	G/T	0.427727	0.175821	intron-variant	N4BP2	GRCh38.p7	4:40145222	TCCAGTAGTTTTTTT[G/T]TTTGTTTGTTTCTTT	55728
rs1985722	snp	G/T	0.464309	0.12873	intron-variant	N4BP2	GRCh38.p7	4:40145226	GTAGTTTTTTTGTTT[G/T]TTTGTTTCTTTTTCT	55728
rs1996559	snp	C/T	0.255782	0.249933	intron-variant	N4BP2	GRCh38.p7	4:40145748	GTGTGTCTTTTTCAC[C/T]ACCTTATCCTTGATG	55728
rs2012638	snp	A/C	0.208779	0.246578	intron-variant	N4BP2	GRCh38.p7	4:40109458	cgcggtggctcatgc[A/C]tgtaattccagcact	55728
rs2055821	snp	A/T	0.201418	0.245234	intron-variant	N4BP2	GRCh38.p7	4:40119170	actctgctcataaaa[A/T]tcttataaggattat	55728
rs2136563	snp	A/G	0.0376037	0.131863	intron-variant	N4BP2	GRCh38.p7	4:40117192	ttctcttctctttcc[A/G]ggacttagattagat	55728
rs2136565	snp	A/T	0.0205511	0.0992634	intron-variant	N4BP2	GRCh38.p7	4:40146921	TTAtttttatttttt[A/T]attttttttattgat	55728
rs2137103	snp	C/T	0.276534	0.248588	intron-variant	N4BP2	GRCh38.p7	4:40180348	AATTAATCAGCAAGA[C/T]ACCACTTTTCAACTA	55728
rs2252352	snp	C/T	0.26518	0.249539	intron-variant	N4BP2	GRCh38.p7	4:40126470	AAATTATACTTAAAA[C/T]ATTTTTCAATTTTAA	55728
rs2271395	snp	C/T	0.157647	0.232316	missense, nc-transcript-variant	N4BP2	GRCh38.p7	4:40137056	TAGACTTCTGGCCAG[C/T]ATGAGATGTGACATT	55728
rs2381486	snp	A/G	0.226779	0.248919	intron-variant	N4BP2	GRCh38.p7	4:40081571	GGATTGCTTGAACGC[A/G]GGAGCTGGAGGTTGT	55728
rs2381488	snp	G/T	0.00318978	0.0398085	intron-variant	N4BP2	GRCh38.p7	4:40143254	AACATTAATTTTTTT[G/T]GGGAAGTAAAATTTC	55728

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