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
rs9713	snp	A/T	0.46865	0.121211	utr-variant-5-prime	PSMD14	GRCh38.p7	2:161308497	CGCCGGTTTGCAGAC[A/T]GAGCCGCGTCGGGTG	10213
rs1064576	snp	A/G	0.0569829	0.158885	utr-variant-3-prime	PSMD14	GRCh38.p7	2:161411597	TTTGCAGATTCTAAA[A/G]TTATACATGAATACA	10213
rs1110587	snp	C/T	0.0803491	0.183626	intron-variant	PSMD14	GRCh38.p7	2:161407766	CACCACCATCTCACC[C/T]CCTTTTGTAACTCTT	10213
rs1111416	snp	C/T	0.11963	0.213316	intron-variant	PSMD14	GRCh38.p7	2:161355716	GTTTTAAAACATAAA[C/T]GAGTTAATACACCTT	10213
rs1111417	snp	C/T	0.121717	0.214577	intron-variant	PSMD14	GRCh38.p7	2:161352474	GTGTAGTTTATTATT[C/T]TAGTGGCAAAATAAA	10213
rs1116165	snp	A/G	9.73492e-05	0.00697604	intron-variant	PSMD14	GRCh38.p7	2:161318779	TTCCTAAGCACAAAA[A/G]TGTTTATTCAATTGC	10213
rs1116173	snp	C/T	0.386123	0.209692	intron-variant	PSMD14	GRCh38.p7	2:161370327	GATATACTAGACAGG[C/T]GGTGCATGGCACTGA	10213
rs1136548	snp	C/T			utr-variant-5-prime	PSMD14	GRCh38.p7	2:161316490	ACCTGCCAGAATTAG[C/T]AAGAGCTTTCTTTAA	10213
rs1559496	snp	C/G	0.470327	0.118136	intron-variant	PSMD14	GRCh38.p7	2:161358583	TCATTAATCTGACCA[C/G]TCCTACTCTACATTT	10213
rs1862953	snp	A/T	0.121022	0.21416	intron-variant	PSMD14	GRCh38.p7	2:161350294	GTATGTCCCAAATAC[A/T]GCCTGGGATGTACTT	10213
rs1863177	snp	A/T	0.244205	0.249933	intron-variant	PSMD14	GRCh38.p7	2:161401288	CAGTAAGGCTTTCAG[A/T]CAACAGTAGGCTATT	10213
rs1882366	snp	A/T			intron-variant	PSMD14	GRCh38.p7	2:161406627	AGATATTCCAAATCA[A/T]ATGCCTACATATTTT	10213
rs1921674	snp	C/T	0.245061	0.249951	intron-variant	PSMD14	GRCh38.p7	2:161391261	TATGTGATTTAAATT[C/T]GAATTTTTGACCTCT	10213
rs2013879	snp	A/G	0.352287	0.228117	intron-variant	PSMD14	GRCh38.p7	2:161319533	ATGACTGCACAGATC[A/G]AAAGTGTCGAACTCA	10213
rs2018759	snp	A/G	0.295088	0.245901	intron-variant	PSMD14	GRCh38.p7	2:161407704	ATTATAAAGTTCAGA[A/G]TATCCAAATCTAACC	10213
rs2042488	snp	A/G	0.121022	0.21416	intron-variant	PSMD14	GRCh38.p7	2:161344180	tactgagggatgact[A/G]TACTCAGAAGTGAAG	10213
rs2042489	snp	A/G	0.261884	0.249717	intron-variant	PSMD14	GRCh38.p7	2:161368658	CTTAGAAAAATATGC[A/G]TGTATTTTTCCAAGC	10213
rs2059337	snp	A/G	0.121022	0.21416	intron-variant	PSMD14	GRCh38.p7	2:161310502	TCATTTTGACATTTC[A/G]TATTCTGCTTTGTGT	10213
rs2113480	snp	C/T	0.383824	0.211166	intron-variant	PSMD14	GRCh38.p7	2:161330099	TGCAATTATGATAAA[C/T]AAATTTGTTCAAGTT	10213
rs2194726	snp	C/T	0.135825	0.222405	intron-variant	PSMD14	GRCh38.p7	2:161389321	AAGCTCCACTCTCTA[C/T]GCCAGACTATGTCTG	10213
rs2194727	snp	C/G	0.135484	0.22223	intron-variant	PSMD14	GRCh38.p7	2:161389360	ACTGAGCACCTTTTT[C/G]TAATTCTCTACCAGG	10213
rs2194728	snp	A/G	0.121022	0.21416	intron-variant	PSMD14	GRCh38.p7	2:161389513	TGATTATTGAAATGA[A/G]TAAGGATTTAATATA	10213
rs2194729	snp	C/T	0.233235	0.249437	intron-variant	PSMD14	GRCh38.p7	2:161392937	TCAATTTTTCTTTCT[C/T]TTTTTTTGGGGAGTA	10213
rs2216941	snp	A/T	0.121022	0.21416	intron-variant	PSMD14	GRCh38.p7	2:161402194	TCTCCAGTCTTTCCC[A/T]TTCAAATCAATTTTC	10213
rs2278077	snp	C/T	0.00119737	0.0244387	intron-variant	PSMD14	GRCh38.p7	2:161308800	AGGTCTGGATGTCGC[C/T]TCCTTTCTCCATTCT	10213
rs2288099	snp	A/G	0	0	intron-variant	PSMD14	GRCh38.p7	2:161367744	GAACCAGAGACCTCA[A/G]CGAAATTTGCTTTGT	10213
rs2303318	snp	A/C	0.339203	0.233544	intron-variant	PSMD14	GRCh38.p7	2:161367984	AAACTAACTCTCATC[A/C]TATTACATTTTCTCT	10213
rs2303319	snp	C/T	0.132066	0.220435	intron-variant	PSMD14	GRCh38.p7	2:161368153	GTCCTTCGGCTTAAA[C/T]TGGTGTAAAATACTG	10213
rs3207471	snp	A/C			intron-variant	PSMD14	GRCh38.p7	2:161339518	TTGAGTAGATGATCT[A/C]AAAAAAAAAAAAAAA	10213
rs3213812	snp	C/T	0.0418186	0.138422	intron-variant	PSMD14	GRCh38.p7	2:161316611	TTAATTATTATTTTA[C/T]GGATGGATAGAGAGA	10213
rs3769957	snp	A/T	0.489837	0.0705577	intron-variant	PSMD14	GRCh38.p7	2:161407333	TCTAGACAGAGAATA[A/T]GCTCATTTTCAGAGT	10213
rs3769958	snp	A/G	0.241627	0.24986	intron-variant	PSMD14	GRCh38.p7	2:161404878	CAGAAGAGCAGAAAG[A/G]CAAGGGCTGAATCTT	10213
rs3769959	snp	C/T	0.135825	0.222405	intron-variant	PSMD14	GRCh38.p7	2:161392695	TAGAAGAGAGCATTA[C/T]AAGATCCCCTTGCGC	10213
rs3769960	snp	C/T	0.00119737	0.0244387	intron-variant	PSMD14	GRCh38.p7	2:161386279	TAATCTTTAGAGTAG[C/T]AATTAACTAGATAGA	10213
rs3769961	snp	G/T	0.0479149	0.147179	intron-variant	PSMD14	GRCh38.p7	2:161356660	TTTTTAAAAGTCTGT[G/T]AAAATATATGCTTTA	10213
rs3769962	snp	C/T	0	0	intron-variant	PSMD14	GRCh38.p7	2:161351070	ATTCAAACAAATGAA[C/T]AGAGTAATAAATTCC	10213
rs3769963	snp	C/T	0.320814	0.239761	intron-variant	PSMD14	GRCh38.p7	2:161350999	ATTTACTAAGGGAGA[C/T]TGGACAAAGGAGGAC	10213
rs3769964	snp	A/G	0.148326	0.228391	intron-variant	PSMD14	GRCh38.p7	2:161350835	GTTTTGCCTTAGGCA[A/G]CAGAGTAACTATCAA	10213
rs3769965	snp	C/T	0.00318978	0.0398085	intron-variant	PSMD14	GRCh38.p7	2:161332139	ATAAAGAAAATCCCT[C/T]CTAAATATTTTAATT	10213
rs3769967	snp	A/G	0.25801	0.249872	intron-variant	PSMD14	GRCh38.p7	2:161318062	TGATTTAGTTTTAAC[A/G]TTTAGAGTAACTACA	10213
rs3769968	snp	G/T	0.329783	0.236927	intron-variant	PSMD14	GRCh38.p7	2:161309640	AACCACTATATATCT[G/T]AACCTCTAAACTTCA	10213
rs3835938	in-del	-/T			intron-variant	PSMD14	GRCh38.p7	2:161390831	GTCAGAGATAAGGTT[-/T]GATCTTATCATAAGC	10213
rs3841876	in-del	-/ATTT			intron-variant	PSMD14	GRCh38.p7	2:161330100	TAAGAACTTGAACAA[-/ATTT]ATTTATCATAATTGC	10213
rs4027148	in-del	-/AT	0.0460142	0.144533	intron-variant	PSMD14	GRCh38.p7	2:161319036	GCAACACTAGATAAC[-/AT]GTGGAAAACATTTAT	10213
rs4027149	snp	C/T	0.121022	0.21416	intron-variant	PSMD14	GRCh38.p7	2:161340634	GGGCCAAAGGTGTTC[C/T]CAGGATCCTGCTAGC	10213
rs4027150	in-del	-/T	0.0766824	0.180169	intron-variant	PSMD14	GRCh38.p7	2:161356777	AAATATTCAAACTCC[-/T]TTTTTTTTTTTTTTA	10213
rs4027152	snp	A/G	0.466927	0.124269	intron-variant	PSMD14	GRCh38.p7	2:161402911	AATGAAAAATAACAA[A/G]TGTTGCCAAGGGTAT	10213
rs4119067	snp	C/G	0	0	intron-variant	PSMD14	GRCh38.p7	2:161340294	CAACCAAGCCAGCCA[C/G]AGAGAGAAGTGGGTT	10213
rs4119068	snp	A/G			intron-variant	PSMD14	GRCh38.p7	2:161340434	AGGGCAAAAGAGGGG[A/G]GACTGGAGTGAAAGT	10213
rs4119069	snp	G/T			intron-variant	PSMD14	GRCh38.p7	2:161340472	GCTTTTAAAATGTTC[G/T]TTTTATCTAAGGTGT	10213
rs4664044	snp	G/T	0.255503	0.249939	intron-variant	PSMD14	GRCh38.p7	2:161313120	ggaggagagaggtaa[G/T]ttactcaaggacagg	10213
rs4664417	snp	A/G	0.46885	0.12085	intron-variant	PSMD14	GRCh38.p7	2:161322682	GATGTGAACCATTGC[A/G]CCCGGCCTGGTCATG	10213
rs4664418	snp	C/T	0.121022	0.21416	intron-variant	PSMD14	GRCh38.p7	2:161337530	TGGTCTTTCTAATTC[C/T]AAAGTATCTCTGCAC	10213
rs4664419	snp	A/G	0.492727	0.0598633	intron-variant	PSMD14	GRCh38.p7	2:161344554	AGAAAGTGTCATATT[A/G]TTTTTCACAGCGAAT	10213
rs4664420	snp	A/G	0.466618	0.124806	intron-variant	PSMD14	GRCh38.p7	2:161364414	ggaaatgcaacattt[A/G]gggaggaaaacaaaa	10213
rs4664421	snp	A/G	0.121022	0.21416	intron-variant	PSMD14	GRCh38.p7	2:161372550	CTATCCACAAAAACA[A/G]TAATAGAAACTGATA	10213
rs4664422	snp	C/G	0.121022	0.21416	intron-variant	PSMD14	GRCh38.p7	2:161392317	GTTAGTGAGACCGCT[C/G]TCAAGTCAGAAAGTG	10213
rs6432678	snp	A/G	0.121717	0.214577	intron-variant	PSMD14	GRCh38.p7	2:161351502	ATATTACTTTTTGTA[A/G]GGTGTTCTCTGTAAA	10213
rs6432679	snp	C/T	0.493613	0.0561475	intron-variant	PSMD14	GRCh38.p7	2:161351747	CTGGGTGCTCTGTTC[C/T]GTGGTATCATTACTG	10213
rs6432681	snp	A/G	0.000798403	0.0199641	intron-variant	PSMD14	GRCh38.p7	2:161410650	TAAAGGATTGCACCT[A/G]TATAATTTGCTATGA	10213
rs6709356	snp	A/G	0.492679	0.0600586	intron-variant	PSMD14	GRCh38.p7	2:161355219	CCTAGGTATATTTCA[A/G]CAGTGGGTGAAATTA	10213
rs6710414	snp	G/T	0.338523	0.233803	downstream-variant-500B	PSMD14	GRCh38.p7	2:161412004	AGGATTTTGGAAGAG[G/T]ACATTTACAAAGAAA	10213
rs6710747	snp	C/G	0.121022	0.21416	intron-variant	PSMD14	GRCh38.p7	2:161320179	GGTGGTATGTAGATA[C/G]TGCAGATTTACCTGC	10213
rs6713728	snp	C/G	0.121717	0.214577	intron-variant	PSMD14	GRCh38.p7	2:161326290	cccacctcggcctcc[C/G]aaagtgctgggatta	10213
rs6713971	snp	A/G	0.0558544	0.157504	intron-variant	PSMD14	GRCh38.p7	2:161326454	tcttgtacattgatg[A/G]tagaaatgtaaaatg	10213
rs6719721	snp	G/T	0.121022	0.21416	intron-variant	PSMD14	GRCh38.p7	2:161374009	AAAAATTAGGGCCAA[G/T]GAGATTGCTTTGCCA	10213
rs6722186	snp	C/T	0.0551013	0.156571	intron-variant	PSMD14	GRCh38.p7	2:161358824	catgtacctgtaatc[C/T]cagctacttgggagg	10213
rs6723514	snp	A/C	0	0	intron-variant	PSMD14	GRCh38.p7	2:161316680	ATGAATGTGATTGAT[A/C]ACCAGATTTTGAAAA	10213
rs6725325	snp	A/G	0.000399281	0.0141238	intron-variant	PSMD14	GRCh38.p7	2:161364925	cctgggcaacacagg[A/G]aaaccccatccctac	10213
rs6727917	snp	A/G	0.4661	0.125701	intron-variant	PSMD14	GRCh38.p7	2:161378097	GGACTTAGTTTTGTC[A/G]GGTTTAATGTCTTCT	10213
rs6733456	snp	C/T	0.48955	0.071525	intron-variant	PSMD14	GRCh38.p7	2:161401922	GTGTATGGCTAGAGG[C/T]AAGTCAGCCTCTCTG	10213
rs6734935	snp	C/T	0.121717	0.214577	intron-variant	PSMD14	GRCh38.p7	2:161323068	TTAAACCTTTTCTTC[C/T]ATTTATTTCTAGAAT	10213
rs6738264	snp	C/T	0.121022	0.21416	intron-variant	PSMD14	GRCh38.p7	2:161383743	CTCCTAAATATTTAC[C/T]GTTAACAGTTAGGGT	10213
rs6738798	snp	C/T	0.00279162	0.0372561	intron-variant	PSMD14	GRCh38.p7	2:161333077	AGCATCTGTCTTGTA[C/T]ATTTTTGAAGGATTT	10213
rs6744214	snp	C/T	0.468349	0.121752	intron-variant	PSMD14	GRCh38.p7	2:161335777	GTAGTTAGCCTGATA[C/T]GGTAGAAAGAATACA	10213
rs6748704	snp	C/T	0.121022	0.21416	intron-variant	PSMD14	GRCh38.p7	2:161331208	TGTGATTTCTGGTTA[C/T]TGTATTCATTTCCTG	10213
rs6755769	snp	G/T	0.121022	0.21416	intron-variant	PSMD14	GRCh38.p7	2:161347191	ttgttgcttgatcag[G/T]gtcttacaaactatt	10213
rs6755815	snp	C/T	0.257176	0.249897	intron-variant	PSMD14	GRCh38.p7	2:161347385	aactactcaaggaat[C/T]ctcctgctccagtct	10213
rs7349280	snp	C/T	0.303438	0.244222	intron-variant	PSMD14	GRCh38.p7	2:161354120	TGTTCTGTTATGAGA[C/T]GTTCAGGTTCTGCTT	10213
rs7421731	snp	C/T			intron-variant	PSMD14	GRCh38.p7	2:161355569	gtctttctttttttc[C/T]ttTAAAGAATTAATG	10213
rs7566586	snp	C/G	0.0569829	0.158885	intron-variant	PSMD14	GRCh38.p7	2:161351912	tagggaagtgcagtc[C/G]tactatgtgcctgag	10213
rs7574882	snp	C/T	0.223225	0.248562	intron-variant	PSMD14	GRCh38.p7	2:161399267	TAGTAAGAATATTAA[C/T]GTGAGCTTTGAAAAA	10213
rs7578146	snp	C/T	0.121369	0.214369	intron-variant	PSMD14	GRCh38.p7	2:161405831	TGGCATGTTATAGTG[C/T]GAACAAAGTTAACAT	10213
rs7586485	snp	A/G	0.244205	0.249933	intron-variant	PSMD14	GRCh38.p7	2:161402429	aggatcatcacttga[A/G]cccaggagttcaagg	10213
rs7589726	snp	A/C	0.121022	0.21416	intron-variant	PSMD14	GRCh38.p7	2:161338203	CCTAGAATTTCTCTC[A/C]AAGAATCCTTGGAAC	10213
rs7595718	snp	A/G	0.121717	0.214577	intron-variant	PSMD14	GRCh38.p7	2:161352199	AAGTTTATATCAGTG[A/G]TTTTCAACCTTGGCT	10213
rs7605885	snp	A/G	0.0551013	0.156571	intron-variant	PSMD14	GRCh38.p7	2:161312971	GATGGGGTTGCCAAT[A/G]acagtagctagtgtt	10213
rs10170291	snp	A/T	0.474544	0.10991	intron-variant	PSMD14	GRCh38.p7	2:161313357	attaattaattaatt[A/T]atttatttttgagat	10213
rs10174431	snp	A/G			intron-variant	PSMD14	GRCh38.p7	2:161344566	Attgtttttcacagc[A/G]aatgattatctttta	10213
rs10182431	snp	A/G	0.121022	0.21416	intron-variant	PSMD14	GRCh38.p7	2:161341878	aaaaaaaatatatat[A/G]tatatataaatttgt	10213
rs10193429	snp	C/T	0.122411	0.214991	intron-variant	PSMD14	GRCh38.p7	2:161385715	AGAATTGTGGAAATA[C/T]TGTTGTAAAAATTAG	10213
rs10197817	snp	C/T	0.470132	0.118498	intron-variant	PSMD14	GRCh38.p7	2:161342482	ttggttgatataata[C/T]aggcgttcagctttc	10213
rs10206910	snp	C/T			intron-variant	PSMD14	GRCh38.p7	2:161389879	tgtcttattttcttt[C/T]tttTTTGTTGTTTTT	10213
rs10207096	snp	G/T			intron-variant	PSMD14	GRCh38.p7	2:161389886	TTTTCTTTCTTTTTT[G/T]TTGTTTTTTTTTTTT	10213
rs10207098	snp	G/T			intron-variant	PSMD14	GRCh38.p7	2:161389889	TCTTTCTTTTTTGTT[G/T]TTTTTTTTTTTTTTT	10213
rs10210533	snp	C/T	0.491577	0.0643472	intron-variant	PSMD14	GRCh38.p7	2:161311171	aaaattagccgggca[C/T]gggggcgtgtgcctg	10213
rs10469684	snp	G/T	0.46855	0.121392	intron-variant	PSMD14	GRCh38.p7	2:161326996	agaaacctgttgata[G/T]ggagggctgattgta	10213
rs10490567	snp	C/T	0.3512	0.228601	intron-variant	PSMD14	GRCh38.p7	2:161317267	GTTAAGATCGTGAAG[C/T]GGAAATTTTGTCTGT	10213
rs10490568	snp	A/G	0.131381	0.220067	intron-variant	PSMD14	GRCh38.p7	2:161395910	AACACCTTCATATTC[A/G]GATTGTCCACACACC	10213
rs10497214	snp	A/C	0.245916	0.249967	intron-variant	PSMD14	GRCh38.p7	2:161369825	ACGAAATAATTGAAC[A/C]AACCATAACTATTGG	10213

Full records

It may take some time, please wait.