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
rs7655	snp	A/G	0.113685	0.209567	utr-variant-3-prime	USP12	GRCh38.p7	13:27066377	CTGGGAGGCTAAAGC[A/G]CTCATGTCCTGGCTC	219333
rs9901	snp	A/T	0.495213	0.048687	intron-variant	USP12	GRCh38.p7	13:27072462	GATGCCTAAGAAACA[A/T]CTTCCTTAGGTGGAA	219333
rs472339	snp	A/T	0.135143	0.222054	intron-variant	USP12	GRCh38.p7	13:27109383	actaaactttaatca[A/T]gtctctacgtgtaac	219333
rs479920	snp	A/G	0.0372196	0.131242	intron-variant	USP12	GRCh38.p7	13:27106790	AATGGAGAGATGGAT[A/G]AAAATGAGACTTCTC	219333
rs480523	snp	A/G	0.192401	0.243274	intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27136911	AACATTGGTCAAGAG[A/G]TGTTTTTTGCGTTAA	219333
rs488119	snp	A/T	0.339203	0.233544	intron-variant	USP12	GRCh38.p7	13:27104633	TGTGTATGTGGGGAA[A/T]ATGAACAAATCTTCA	219333
rs488218	snp	C/T	0.185155	0.241444	intron-variant	USP12	GRCh38.p7	13:27104654	CAAATCTTCAACAAA[C/T]GTATCAAATTCAAGA	219333
rs494649	snp	C/T	0.212425	0.24716	intron-variant	USP12	GRCh38.p7	13:27090841	TGTGCTAATAATAAT[C/T]TTGATGTATTAAAAT	219333
rs497224	snp	A/T	0.0941369	0.195465	intron-variant	USP12	GRCh38.p7	13:27085190	gcgagactccatctc[A/T]aaaaaaaaagaaaga	219333
rs497329	snp	G/T	0.0372196	0.131242	intron-variant	USP12	GRCh38.p7	13:27111518	CCCTACTCGAGGTCT[G/T]ATCATTGATTTTTTG	219333
rs505361	snp	C/T	0.177824	0.239355	intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27166245	TTCTCTTTTAGCAGC[C/T]CTATTCCAGAAACTT	219333
rs507243	snp	C/T	0.107694	0.205546	intron-variant	USP12	GRCh38.p7	13:27102275	TTTCTTCCAAAATAA[C/T]AGTAGATCACCCACA	219333
rs507580	snp	C/T	0.109461	0.206758	intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27127725	GTGCTTCTGTGGTGG[C/T]AGTTGAAGGAGAAAG	219333
rs514128	snp	C/T	0.166832	0.235761	intron-variant	USP12	GRCh38.p7	13:27119943	ATTCAAGGTTTTCCT[C/T]AACAGAAATGATCAG	219333
rs515025	snp	A/G	0.0839998	0.186933	intron-variant	USP12	GRCh38.p7	13:27071402	CAGTAAAAAATTTCA[A/G]TAATATAGCTGTATG	219333
rs520344	snp	C/T	0	0	intron-variant	USP12	GRCh38.p7	13:27102315	TGTAAAGAGAGGACT[C/T]catttcctacctggg	219333
rs521995	snp	C/T	0.0748431	0.178382	intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27133167	CAAAAATATCTGATC[C/T]ATTAATAACACAGTC	219333
rs522268	snp	C/T	0.363985	0.222503	intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27164356	ACGTAGCTTTGGACA[C/T]GTGGCTCACTACAGA	219333
rs526413	snp	C/T	0.0655868	0.168795	intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27135450	gggcatgctggctca[C/T]gcctataatcccagc	219333
rs532341	snp	G/T	0.151668	0.229849	intron-variant, upstream-variant-2KB	USP12, USP12-AS1	GRCh38.p7	13:27123915	CTTGAAAAGATGAGG[G/T]CTTGTCCTTTTCACA	219333
rs534542	snp	C/G	0.0494327	0.149241	intron-variant	USP12	GRCh38.p7	13:27102939	ACATGCATGGAGCCA[C/G]TGTTGCTGTACTCTA	219333
rs535947	snp	C/T	0.156319	0.231784	intron-variant	USP12	GRCh38.p7	13:27119060	actataacagaattt[C/T]aacttttctaaggca	219333
rs538344	snp	C/T	0	0	synonymous-codon, utr-variant-5-prime, intron-variant	USP12	GRCh38.p7	13:27105735	AGTAGAATTACCATT[C/T]TCTTTCCGTAATCTT	219333
rs538364	snp	A/G	0	0	intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27159155	CTTCTAAAATTGCAA[A/G]ATTAAAAGAAACTAC	219333
rs556647	snp	A/C/T	0	0	intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27146586	ACCACTGCAGAGCTC[A/C/T]GATGTTGGCTTATAA	219333
rs563184	snp	A/T	0.0475351	0.146656	intron-variant	USP12	GRCh38.p7	13:27093819	aacatttccactgta[A/T]ggatgtgctgcagtt	219333
rs565596	snp	C/T	0.0715223	0.175059	intron-variant	USP12	GRCh38.p7	13:27106383	TACTCCTCTCCACTC[C/T]AGTAATTGGGGCGAG	219333
rs565707	snp	A/C	0.437542	0.165312	intron-variant	USP12	GRCh38.p7	13:27106427	CGGGCGGGGAAATAA[A/C]CCTACTTTATAAAGT	219333
rs568500	snp	A/T	0.17461	0.238362	intron-variant	USP12	GRCh38.p7	13:27106712	ACCATTTATTTTTTT[A/T]AAAAAAATGAGGAAG	219333
rs570248	snp	A/T	0.106987	0.205054	intron-variant	USP12	GRCh38.p7	13:27103878	TATAAAGCCATAAGT[A/T]TGTAACTGTATTTTA	219333
rs571789	snp	C/G	0.0498117	0.149749	intron-variant	USP12	GRCh38.p7	13:27109895	ccagcctgggcgaca[C/G]agtgagactctgtct	219333
rs766870	snp	G/T			intron-variant	USP12	GRCh38.p7	13:27121137	TGGGATTATTACTGG[G/T]TCCCTTATGCATTGA	219333
rs832777	snp	A/T	0.109461	0.206758	intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27128042	GTATTTTCAATGAAA[A/T]GTTTCACCACATAAT	219333
rs832778	snp	A/C	0.290977	0.246619	intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27130539	GTTCTCACACACACA[A/C]AAAAAAAATCACAAA	219333
rs832779	snp	C/T	0.0178098	0.0926698	intron-variant	USP12	GRCh38.p7	13:27087174	CTGACTTCCTGCCCC[C/T]GCTCCCTGAATGcac	219333
rs832780	snp	A/C	0.0372196	0.131242	intron-variant	USP12	GRCh38.p7	13:27085558	AAGTTTATAGTTCTC[A/C]GTCTTGGAATAATAG	219333
rs865574	snp	C/G/T	0.000399281	0.0141238	intron-variant	USP12	GRCh38.p7	13:27087098	cacacacacacacaG[C/G/T]CCCTTCCCCTCTGCT	219333
rs866227	snp	A/T			intron-variant	USP12	GRCh38.p7	13:27087165	TGCCCCTGCTCCCTG[A/T]ATGcacacacatgca	219333
rs866228	snp	C/T			intron-variant	USP12	GRCh38.p7	13:27086667	CAAAAGCCACCCTTT[C/T]CCTAGAATGATGGTT	219333
rs953529	snp	C/T	0.0678174	0.1712	intron-variant	USP12	GRCh38.p7	13:27112499	ACTCTGTTGCCCAGG[C/T]TGGTCTCAGATTTCT	219333
rs970449	snp	C/G			intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27167122	ggcatgtgccaccac[C/G]cccagctaatttttg	219333
rs995424	snp	C/T	0.447032	0.153878	intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27145389	TGTTTCCATGGAACA[C/T]GAATAACAAGCTCCC	219333
rs995425	snp	A/G	0	0	intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27145544	CCTAAACTCAAACTA[A/G]CTCCCACATTAACTT	219333
rs1159036	snp	A/T	0.387832	0.208572	intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27132979	GCAACACAGCCATGC[A/T]CCTACTATGAACTGT	219333
rs1170032	snp	G/T	0.0836354	0.186609	intron-variant	USP12	GRCh38.p7	13:27078477	GAATACAACATGGAT[G/T]CAGTTTGTCATTTTA	219333
rs1170035	snp	A/G	0.0803491	0.183626	intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27137508	TGCTGTAAATAGATA[A/G]ATGTATACTTAAATG	219333
rs1170036	snp	G/T	0.345482	0.231048	intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27137580	AATAATCATAAGTAA[G/T]ATACCACACTGATTA	219333
rs1170037	snp	C/T	0.0807149	0.183963	intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27137726	gcctcccctggaata[C/T]gggcaggacctgtga	219333
rs1170038	snp	C/T	0.339203	0.233544	intron-variant	USP12	GRCh38.p7	13:27100631	CAATCCCGTACAATT[C/T]AAGAACCTTTATCTC	219333
rs1170039	snp	A/G	0.029116	0.117091	intron-variant	USP12	GRCh38.p7	13:27107096	ttgggaggccgaggc[A/G]ggcggatcacttgag	219333
rs1180172	snp	A/T			intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27166110	TGGGAAAGTTTCTTA[A/T]AACTTCGAGTTAATT	219333
rs1186393	snp	A/T	0	0	intron-variant	USP12	GRCh38.p7	13:27100541	ATGGCCTGATTCAGT[A/T]TCTCTCTCCACTTTG	219333
rs1318659	snp	C/T	0.0150606	0.0854603	intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27130448	atggatgactgcaag[C/T]ctcaaaaaagcaatc	219333
rs1327306	snp	A/G	0.291235	0.246576	intron-variant	USP12	GRCh38.p7	13:27096146	GTTGAAATATTTGTG[A/G]AATAATAAGTCAGGT	219333
rs1327307	snp	C/G	0.386313	0.209568	intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27128093	GAGAATATTTAGAGA[C/G]AACAAAAGAAGATTC	219333
rs1473758	snp	A/G	0.121022	0.21416	intron-variant, upstream-variant-2KB	USP12, USP12-AS1	GRCh38.p7	13:27124886	AATCAAAGGCAATGA[A/G]AATATTTATGACAAA	219333
rs1547189	snp	A/G	0.391024	0.206427	intron-variant	USP12	GRCh38.p7	13:27091268	TTACATGTAAATTCC[A/G]GCCTGATCTGGCTAG	219333
rs1555976	snp	A/G			intron-variant	USP12	GRCh38.p7	13:27121083	GGGAGGACAACAGGA[A/G]AGATGAGCATGAAGC	219333
rs1629464	snp	G/T			intron-variant	USP12	GRCh38.p7	13:27093884	ccttaaaaagacatg[G/T]aagaaccttaaatgc	219333
rs1751773	snp	C/T	0.154329	0.23097	intron-variant	USP12	GRCh38.p7	13:27123267	gtaacaaatcattct[C/T]tccagacctcagttt	219333
rs1762075	snp	A/G			intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27158523	tcaaacctagatggt[A/G]cagcccactacacac	219333
rs1762079	snp	C/T	0.0372196	0.131242	intron-variant	USP12	GRCh38.p7	13:27113703	GCCCCTAAAACAGGG[C/T]TGGACGCTTGGTACA	219333
rs1960195	snp	A/G	0.335101	0.23507	intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27139632	CAGAAATAAAAATAT[A/G]GTCACTCTTGTATAA	219333
rs1999667	snp	C/G	0.0360663	0.129354	intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27164368	ACACGTGGCTCACTA[C/G]AGATAAATAAAGCAA	219333
rs2104580	snp	A/G	0.115788	0.21092	intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27167830	GGAAAGCTGGGGCAA[A/G]CCTCAGAGCCCATGC	219333
rs2148755	snp	C/T	0.0785177	0.181917	intron-variant	USP12	GRCh38.p7	13:27072338	GTAAGGACTGGTAAA[C/T]TGAAAAAAGTTAGGC	219333
rs2182669	snp	C/T	0.0310518	0.120672	upstream-variant-2KB, intron-variant	USP12, USP12-AS2	GRCh38.p7	13:27173803	actgggattgtgcca[C/T]tgcaccccagcctgg	219333
rs2478922	snp	G/T	0.111224	0.207945	intron-variant	USP12	GRCh38.p7	13:27096520	GCTTTACCCTGTGCT[G/T]GGCAATATACAACTC	219333
rs2478929	snp	A/G	0.0839998	0.186933	intron-variant	USP12	GRCh38.p7	13:27079399	ACCTGTCAGTGACTG[A/G]TCAAAGACTTGGAAT	219333
rs2484110	snp	C/T	0.499587	0.0143711	intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27155332	GTGATCTGCCCGCCT[C/T]GGCCTCCCAAGGTGC	219333
rs2484111	snp	C/T	0.321769	0.239477	intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27158833	GAAGATCATGGGAAA[C/T]TAAAATGCACACAAG	219333
rs2484112	snp	C/T	0.188	0.24219	intron-variant	USP12	GRCh38.p7	13:27069509	TGGAACTCTCACACA[C/T]AGCTGGCAGGGCACA	219333
rs2484113	snp	C/T	0.0839998	0.186933	intron-variant	USP12	GRCh38.p7	13:27070416	gtgtgtgagtatgGC[C/T]ATTTTATTCTTTTTT	219333
rs2484114	snp	G/T	0.29046	0.246704	intron-variant	USP12	GRCh38.p7	13:27074878	CTCAGAAGTGATTTA[G/T]TTTAACCAACAACCC	219333
rs2484115	snp	A/T	0.110167	0.207236	intron-variant	USP12	GRCh38.p7	13:27096990	GTATTAGAAATCTTT[A/T]AAAAAGTTTTAAAAA	219333
rs2484116	snp	C/T	0.170733	0.237101	intron-variant	USP12	GRCh38.p7	13:27112716	GATGCCATCAACCCT[C/T]TGACATCATGGAACT	219333
rs2497960	snp	C/T	0.0865458	0.189163	intron-variant	USP12	GRCh38.p7	13:27115542	GCAGGTGTTTTAAAA[C/T]GCATATATTGATAAA	219333
rs2497961	snp	C/T	0.0475351	0.146656	intron-variant	USP12	GRCh38.p7	13:27097078	CCATTTATAAGATTG[C/T]CCAGTTTGGTTTTCT	219333
rs2497962	snp	A/G	0.139225	0.224118	intron-variant	USP12	GRCh38.p7	13:27096624	TCTCGTCCCATTTTC[A/G]TGTTTACAAATAAAG	219333
rs2497966	snp	C/T	0.089084	0.191327	intron-variant	USP12	GRCh38.p7	13:27079658	CAATAGTCAGAAACG[C/T]TTTTTAAAGTAAATT	219333
rs2497970	snp	C/T	0.0142736	0.0832652	intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27152351	tgaaccttgaaaaca[C/T]gcaaagtaaaagcag	219333
rs2497971	snp	C/T	0.316243	0.241064	intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27155233	actacaggcgcgtgc[C/T]accatgcccggctaa	219333
rs2497980	snp	C/T	0.0681886	0.171594	intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27147616	TTTGTCTTTGACTTT[C/T]AGCATTTTTATTATC	219333
rs2497981	snp	C/T	0.167158	0.235875	intron-variant	USP12	GRCh38.p7	13:27121172	AAGTCAAGCAAGTTA[C/T]CTTGCTGTTTCTTGT	219333
rs2986635	snp	C/T	0.0659589	0.169201	intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27142389	ATGCATGATCATCTT[C/T]GATACTGGGCATTAC	219333
rs3002289	snp	C/G	0.0138799	0.0821421	intron-variant	USP12	GRCh38.p7	13:27097398	ggctcactgcaacct[C/G]tacctcccgggttca	219333
rs3002291	snp	C/T	0.0174175	0.0916809	intron-variant	USP12	GRCh38.p7	13:27084009	agctgagattacagg[C/T]gcctgccaccatgcc	219333
rs3187469	snp	A/G	0	0	utr-variant-3-prime	USP12	GRCh38.p7	13:27066242	tgtggggattaatta[A/G]agataatgtctgtaa	219333
rs3858763	snp	C/T	0.269267	0.249256	intron-variant	USP12	GRCh38.p7	13:27121237	GGAGAAACATCTTCC[C/T]AAAATTCATAACCAT	219333
rs4238199	snp	A/G	0.463018	0.130857	intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27154600	CAAAATTCATTAAAG[A/G]CATATCAGGAATTGA	219333
rs4597174	snp	A/G	0.0887219	0.191022	intron-variant	USP12	GRCh38.p7	13:27120345	GGATAAAGAGAAGGC[A/G]TGATGGTGAGTTAAG	219333
rs4769540	snp	A/C	0.494057	0.0541878	intron-variant	USP12	GRCh38.p7	13:27094551	cttgactgggtgatc[A/C]aaaattaatttcacc	219333
rs4769541	snp	A/G	0.396909	0.202282	intron-variant	USP12	GRCh38.p7	13:27099194	GATTGAGGAGCTGGG[A/G]AGGAAGCAGAGAGCA	219333
rs4769542	snp	A/G	0.490997	0.0664859	intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27166441	AAGGAGGCAGACTCA[A/G]TTTGGGGGGACTTGG	219333
rs4771069	snp	A/T	0.294064	0.246086	intron-variant	USP12	GRCh38.p7	13:27072893	CTTTCATATGAAGCA[A/T]ATCTACAAATAAGTC	219333
rs4771070	snp	C/T	0.476052	0.106772	intron-variant	USP12	GRCh38.p7	13:27078154	ACTTGGCCCTCCATA[C/T]TGGGAGTTCCACATC	219333
rs4771071	snp	G/T	0.290977	0.246619	intron-variant	USP12	GRCh38.p7	13:27092807	GGACCTTTAGTTTAT[G/T]GATGACTTTTTAGAT	219333
rs4771073	snp	A/G	0.376791	0.215463	intron-variant	USP12	GRCh38.p7	13:27119690	TACTGTTTTAACACA[A/G]AACTCCAGGGAAGTC	219333
rs4771074	snp	A/G	0.44651	0.154543	intron-variant	USP12, USP12-AS1	GRCh38.p7	13:27152959	aaaaaaaaaaaaaaa[A/G]gaaagaaagaaaAGA	219333
rs5802410	snp	A/T			intron-variant	USP12	GRCh38.p7	13:27103607	AACTATCAAAAAAAA[A/T]AATAATAATAATAAT	219333

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