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
rs193204	snp	A/C	0.00716266	0.059414	intron-variant	USP32	GRCh38.p7	17:60184064	ggccaaggcgggtgg[A/C]tcatgaggtcaggag	84669
rs237954	snp	C/G	0.377977	0.21476	intron-variant	USP32	GRCh38.p7	17:60266458	TTAATTTCTAATATT[C/G]AAAACTGATCATTGC	84669
rs237955	snp	A/T	0.287867	0.247116	intron-variant, upstream-variant-2KB	USP32	GRCh38.p7	17:60265861	AATATTTTGAGTAGC[A/T]TAATGTAGTAACTAA	84669
rs237956	snp	A/T	0.363776	0.222609	intron-variant	USP32	GRCh38.p7	17:60263583	GTAGAAACTCCATCT[A/T]ACATAAAAGGCGACA	84669
rs237957	snp	A/G	0.163564	0.234582	intron-variant	USP32	GRCh38.p7	17:60262519	TTGTAAATGTCCTCC[A/G]TTTAAATGTGGCCCT	84669
rs237958	snp	C/T	0.378765	0.214288	intron-variant	USP32	GRCh38.p7	17:60262232	GTTTCACTCTTGTTA[C/T]TCAGGCTGGAGTGCA	84669
rs237959	snp	A/C	0.262159	0.249704	intron-variant	USP32	GRCh38.p7	17:60277636	ATAAGGACAATATAC[A/C]TTTCTTGAGTTAGCT	84669
rs237960	snp	C/T	0.262159	0.249704	intron-variant	USP32	GRCh38.p7	17:60273908	gaggctgcagtgagc[C/T]gagattgcgccactg	84669
rs237961	snp	C/T	0.281313	0.248031	intron-variant	USP32	GRCh38.p7	17:60272033	TTGGTCAGGCTGGTC[C/T]CAAACTCCTGGTCTC	84669
rs237962	snp	C/T	0.282105	0.24793	intron-variant	USP32	GRCh38.p7	17:60271806	CCTGTACTGATTTTT[C/T]TTCTTCTTTTTTTTT	84669
rs237963	snp	A/G	0.288906	0.246954	intron-variant	USP32	GRCh38.p7	17:60267394	aagcaacagtgcgag[A/G]cttcgtctcaaaaaa	84669
rs237964	snp	A/T	0.25634	0.24992	intron-variant	USP32	GRCh38.p7	17:60256183	TCTCTTTGAAAAAAA[A/T]AATAATAAAAATAAA	84669
rs237965	snp	A/C/T	0.02016	0.0983543	intron-variant	USP32	GRCh38.p7	17:60255034	CACTCATCTTTCAGA[A/C/T]GAGTAATGTAGTTCt	84669
rs237966	snp	C/T	0.257176	0.249897	intron-variant	USP32	GRCh38.p7	17:60255022	AACTTCAGCAAGCAC[C/T]CATCTTTCAGACGAG	84669
rs237967	snp	A/G	0.35445	0.227135	intron-variant	USP32	GRCh38.p7	17:60253886	TTTTATAAAGCCATC[A/G]ACTTGAATCTATGCT	84669
rs237968	snp	A/T	0.358303	0.225323	intron-variant	USP32	GRCh38.p7	17:60250022	TGAATAAACAAATTT[A/T]AAAAAAAACCCACAG	84669
rs237969	snp	A/G	0.46137	0.133501	intron-variant	USP32	GRCh38.p7	17:60248507	ttggtagacttgatc[A/G]tgttccaacttctgt	84669
rs345173	snp	C/T	0.268452	0.249318	intron-variant	USP32	GRCh38.p7	17:60184665	agtacaaaaattagc[C/T]gggtggtagtggtgc	84669
rs345174	snp	A/T	0.281577	0.247998	intron-variant	USP32	GRCh38.p7	17:60182794	aaaataaaataaatt[A/T]aaaaaaaaagagttt	84669
rs345175	snp	C/T	0.257176	0.249897	intron-variant	USP32	GRCh38.p7	17:60181115	GCTCAAGTGATCCTC[C/T]TGCCTCAGCCTTCTA	84669
rs345176	snp	A/G	0.354881	0.226936	downstream-variant-500B, intron-variant, nc-transcript-variant	USP32, CA4	GRCh38.p7	17:60177042	TTCCTAACAGGCCAC[A/G]GATGGTACTGGTCTG	84669
rs703790	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	USP32, CA4	GRCh38.p7	17:60177464	AATTCATGAACTAGC[A/G]GAAAATTTATTAAAT	84669
rs963142	snp	A/T	0.0197687	0.0974348	intron-variant	USP32	GRCh38.p7	17:60228666	ttacaaaaaaatatt[A/T]aaaaaaaatagtggg	84669
rs964332	snp	G/T	0.135484	0.22223	intron-variant	USP32	GRCh38.p7	17:60270087	TCTCTTTGTACTGTT[G/T]AATCTTTTATACATG	84669
rs1053535	snp	A/G	0	0	utr-variant-3-prime, intron-variant, nc-transcript-variant	USP32, CA4	GRCh38.p7	17:60177695	AAAATATAATTGCAA[A/G]TAGGTAGGACTGGCC	84669
rs1053537	snp	A/G	0	0	utr-variant-3-prime, intron-variant, nc-transcript-variant	USP32, CA4	GRCh38.p7	17:60177673	GGACTGGCCTAAATT[A/G]TCTAATGTAATAAAG	84669
rs1053621	snp	A/G			missense, downstream-variant-500B	USP32, CA4	GRCh38.p7	17:60179368	TTCTATGAGCAGCAG[A/G]GGATAGACTATGCAC	84669
rs1053622	snp	C/T	0	0	synonymous-codon, downstream-variant-500B	USP32, CA4	GRCh38.p7	17:60179357	GCAGGGGATAGACTA[C/T]GCACAATTTCTGCCA	84669
rs1053625	snp	C/T			missense, downstream-variant-500B	USP32, CA4	GRCh38.p7	17:60179337	AATTTCTGCCAAAGA[C/T]TGATGGCAAAAAGAT	84669
rs1061592	snp	A/G	0	0	intron-variant	USP32	GRCh38.p7	17:60376892	TATAACTTCATATAT[A/G]GAAGAAAACTTTTAT	84669
rs1063880	snp	C/T			synonymous-codon	USP32	GRCh38.p7	17:60181500	GGCAGCCAACCAGAG[C/T]TGGTCACTCCTCAGG	84669
rs1132900	snp	C/T	0	0	synonymous-codon	USP32	GRCh38.p7	17:60180566	CTGCAAGTGGTACTG[C/T]TACAATGACAGCAGC	84669
rs1138677	snp	C/T			intron-variant	USP32	GRCh38.p7	17:60376610	cttgaatccgggagg[C/T]agaggttgcaatgag	84669
rs1142748	snp	A/G	4.94654e-05	0.00497295	synonymous-codon, downstream-variant-500B	USP32, CA4	GRCh38.p7	17:60179417	TCAGGAACTTCACCC[A/G]GATGAAATTGACACC	84669
rs1385176	snp	C/T	0.5	0	intron-variant	USP32	GRCh38.p7	17:60228501	TTCTTTTTTCTTTTT[C/T]TTTTTTTTTTTTTTT	84669
rs1989898	snp	A/G			intron-variant	USP32	GRCh38.p7	17:60252689	AGGGAAGAGAAAGGG[A/G]AGGGAGAAAAAGCGA	84669
rs1989899	snp	A/G			intron-variant	USP32	GRCh38.p7	17:60252693	AAGAGAAAGGGGAGG[A/G]AGAAAAAGCGAAAGG	84669
rs2258523	snp	A/G			intron-variant	USP32	GRCh38.p7	17:60217110	CTATAAAAACTTTCT[A/G]AAACTCAAATTTTCA	84669
rs2258710	snp	C/T			intron-variant	USP32	GRCh38.p7	17:60220675	gcctgggtgacagag[C/T]gagactgtgtctcaa	84669
rs2258711	snp	A/G			intron-variant	USP32	GRCh38.p7	17:60220755	ttgggaggctgaggc[A/G]ggagaatggcaagaa	84669
rs2259538	snp	A/G			intron-variant	USP32	GRCh38.p7	17:60202587	gaaatattggaagga[A/G]taaaccatgttcatg	84669
rs2306672	snp	C/T	0.000263796	0.0114816	intron-variant	USP32	GRCh38.p7	17:60222395	TTATATAAGGCACTA[C/T]TAACTATACTTACTG	84669
rs2333671	snp	C/T	0.467439	0.123371	intron-variant	USP32	GRCh38.p7	17:60237289	gggactacaggtgtg[C/T]gctatgcccagctaa	84669
rs2333672	snp	A/C	0.0197687	0.0974348	intron-variant	USP32	GRCh38.p7	17:60241044	gctctgttgcccagg[A/C]tggagtgcagtggct	84669
rs2333673	snp	C/T	0.467744	0.122832	intron-variant	USP32	GRCh38.p7	17:60266943	ACAGGCGTGAGCCAC[C/T]GTGCCCGGCCAATTT	84669
rs2333674	snp	C/T			intron-variant	USP32, LOC105371850	GRCh38.p7	17:60413855	ggcgacagttagatt[C/T]tgtttcaaaaaaaaa	84669
rs2333675	snp	C/T	0.5	0	intron-variant	USP32	GRCh38.p7	17:60376996	GCACAAAGAACATTG[C/T]CATAATAAACTTTTG	84669
rs2333676	snp	C/G			intron-variant, upstream-variant-2KB	USP32	GRCh38.p7	17:60377362	TTTTAAAAGTGCCTA[C/G]AAAAGCAGAAGATTT	84669
rs2333677	snp	C/T	0.0294919	0.117797	intron-variant	USP32	GRCh38.p7	17:60381065	CAATTTACCAGATTA[C/T]TGCTGCTAGTTGTAT	84669
rs2440062	snp	A/G	0.5	0	intron-variant	USP32	GRCh38.p7	17:60219459	ACAGGGCTTAGAACT[A/G]TGGTCATGCACAAGA	84669
rs2458355	snp	C/T	0	0	intron-variant	USP32	GRCh38.p7	17:60208579	GTAAACAAATAACTA[C/T]GCTTACAAATTCAGG	84669
rs2458356	snp	C/T	0	0	intron-variant	USP32	GRCh38.p7	17:60208589	AACTATGCTTACAAA[C/T]TCAGGCTATTTAAAT	84669
rs2468992	snp	A/T	0	0	intron-variant	USP32	GRCh38.p7	17:60219462	TTTACAGGGCTTAGA[A/T]CTATGGTCATGCACA	84669
rs2468993	snp	A/G	0.126909	0.217598	intron-variant	USP32	GRCh38.p7	17:60218125	GTAAGAATTCTTTCA[A/G]TAGTGTTTCGTAGTA	84669
rs2468994	snp	A/G	0.000399281	0.0141238	intron-variant	USP32	GRCh38.p7	17:60218112	CAGTAGTGTTTCGTA[A/G]TAATTATAGCAAAGC	84669
rs2468996	snp	A/G	0	0	intron-variant	USP32	GRCh38.p7	17:60217144	GTATAGTAAGTGGCT[A/G]CCTGCTTAATGAGCT	84669
rs2468997	snp	A/C	0	0	intron-variant	USP32	GRCh38.p7	17:60214962	aacaaacaaacaaac[A/C]aacaaaAAGAACTTG	84669
rs2468998	snp	G/T	0	0	intron-variant	USP32	GRCh38.p7	17:60214922	CCTGCATTTTAAAGC[G/T]TTTTGGTACTCTTCA	84669
rs2468999	snp	C/T	0	0	intron-variant	USP32	GRCh38.p7	17:60201754	GGAGAATCACTTGAA[C/T]CCCAGAGGCAGAGGT	84669
rs2469000	snp	C/T			intron-variant	USP32	GRCh38.p7	17:60201722	GCAATGGGCCGAGAT[C/T]ATGCCATTGCATTCC	84669
rs2469001	snp	A/G			intron-variant	USP32	GRCh38.p7	17:60201172	gatggaaagaagcca[A/G]acacaaaagaatTAg	84669
rs2469002	snp	C/T	0	0	intron-variant	USP32	GRCh38.p7	17:60200985	gtagtcccagctact[C/T]gggaggctgaggcaa	84669
rs2586314	snp	A/C/T	3.46272e-05	0.00416082			GRCh38.p7	17:60211127	ATTTGTCCTAGAAGT[A/C/T]TGAGAGGAAAATTTG	84669
rs2586324	snp	A/G	0.5	0			GRCh38.p7	17:60214441	GGGATTTTACCTATA[A/G]TAATTATGCTAAAAG	84669
rs2627858	snp	A/G			intron-variant	USP32	GRCh38.p7	17:60208437	CAGTGGCTTTGCAGG[A/G]TTTTAAAGAGAGTTG	84669
rs2627860	snp	A/C	0	0	missense	USP32	GRCh38.p7	17:60209492	CCAGAAGTTCTTGGG[A/C]GTCTTGTTGCTGAAA	84669
rs2627862	snp	C/T			intron-variant	USP32	GRCh38.p7	17:60209789	TCCTCAGTTCAGTAT[C/T]ATGTAAGCAAACTGT	84669
rs2627863	snp	C/T			intron-variant	USP32	GRCh38.p7	17:60209839	TATTTAAGACAGAAA[C/T]ATTAAAACAGCGTTT	84669
rs2627865	snp	A/C	0	0	intron-variant	USP32	GRCh38.p7	17:60210073	CTTGTTGCATCCTAA[A/C]TTTTATTAACTGCAT	84669
rs2627866	snp	C/T	0	0	intron-variant	USP32	GRCh38.p7	17:60210342	TTGGAGACAGAGTCT[C/T]ACTCTGTTGCCCAGG	84669
rs2627867	snp	A/G	1.65269e-05	0.00287457	synonymous-codon	USP32	GRCh38.p7	17:60211480	GCATGTGTTTCCCAG[A/G]TTGCTTAGACCTGTG	84669
rs2627869	snp	G/T			intron-variant	USP32	GRCh38.p7	17:60204977	tttttttttttagaa[G/T]agacgaggtctcact	84669
rs2627872	snp	A/G			intron-variant	USP32	GRCh38.p7	17:60213170	ATCTATGAATATACA[A/G]ATAGCTCTGTCAGTG	84669
rs2627873	snp	A/G			intron-variant	USP32	GRCh38.p7	17:60213171	TCTATGAATATACAA[A/G]TAGCTCTGTCAGTGA	84669
rs2627875	snp	A/G	0	0	intron-variant	USP32	GRCh38.p7	17:60214798	ACAGTAATCACAGTA[A/G]GAAAAAAGGCAGATG	84669
rs2627879	snp	A/G			intron-variant	USP32	GRCh38.p7	17:60215928	tggttttgaactcca[A/G]ggctcagggaatcct	84669
rs2627897	snp	A/T			intron-variant	USP32	GRCh38.p7	17:60219055	ATATGTCATTTTGAT[A/T]GGCTTGATGTTTTTT	84669
rs2627898	snp	A/G			intron-variant	USP32	GRCh38.p7	17:60219136	CTCTCTGTCTCTTAT[A/G]TAAAGCCTCTTTAGA	84669
rs2627906	snp	A/C	0.0850919	0.187897	intron-variant	USP32	GRCh38.p7	17:60220597	GTTGTAAGAGTAGTA[A/C]ATGATCAATTTCATA	84669
rs2627913	snp	C/T			intron-variant	USP32	GRCh38.p7	17:60202373	tatcctcatatctta[C/T]tcttcttcaagagta	84669
rs2668964	snp	C/T			intron-variant	USP32	GRCh38.p7	17:60208236	GAAAAGATCTTTTAT[C/T]GGTAAAATGCAGGTT	84669
rs2668965	snp	A/G	0.00597247	0.0543191	intron-variant	USP32	GRCh38.p7	17:60208486	AAAAAACATGCCCCA[A/G]TCTACATCTTTCAAA	84669
rs2668970	snp	A/G	0	0	synonymous-codon	USP32	GRCh38.p7	17:60209511	TTGTTGCTGAAACCC[A/G]TTAAACCTGGGAGCA	84669
rs2668973	snp	A/G	0.5	0	intron-variant	USP32	GRCh38.p7	17:60210261	AAATCTACTACATCT[A/G]ATATTAATATAAAAC	84669
rs2668976	snp	C/T	0	0	intron-variant	USP32	GRCh38.p7	17:60211178	TCACAATCATGTGGG[C/T]GCAAAAATGCCTAGC	84669
rs2668977	snp	A/G	0.5	0	intron-variant	USP32	GRCh38.p7	17:60211297	TTTCTCCCACAGGGT[A/G]AAAAAAGAGGAAATT	84669
rs2668979	snp	A/G	0	0	missense	USP32	GRCh38.p7	17:60211511	GCTCCCTTTTCTGTG[A/G]GAACTGGTATGAGAA	84669
rs2668980	snp	C/T			intron-variant	USP32	GRCh38.p7	17:60211652	TTCTCTAGCAGGTCT[C/T]TGAAATGCTAGAGAA	84669
rs2668995	snp	A/G			intron-variant	USP32	GRCh38.p7	17:60216803	CCGTGATCAGTTTTT[A/G]AACACATAGCAAGCA	84669
rs2677144	snp	A/C	0	0	intron-variant, missense	USP32	GRCh38.p7	17:60377108	CCTACTACTCTCTCT[A/C]TATATATGCCCATTA	84669
rs2877993	snp	A/G	0.365439	0.221752	intron-variant	USP32	GRCh38.p7	17:60224594	GACTGCAACCAGCAC[A/G]GGCAACATGAGACCT	84669
rs2956864	snp	G/T			intron-variant	USP32	GRCh38.p7	17:60214089	ctgggcgtggcggtg[G/T]gagcctgtagtccca	84669
rs2956865	snp	A/G	0.5	0	intron-variant	USP32	GRCh38.p7	17:60214011	AGGTTGCAGTGAGCC[A/G]AGATAGTGCCACTAT	84669
rs3068151	in-del	-/AG			intron-variant	USP32	GRCh38.p7	17:60340352	aggccaaggtgggag[-/AG]gatcatttgagctca	84669
rs3206265	snp	A/G	0.32	0.24	synonymous-codon	USP32	GRCh38.p7	17:60181576	GGATGCCAGCAAAGA[A/G]AATGGGGCTGGGCAG	84669
rs3206266	snp	A/C			synonymous-codon	USP32	GRCh38.p7	17:60181558	TGGGGCTGGGCAGAT[A/C]TGTGAGCTGGCTGAC	84669
rs3207629	snp	C/T	0	0	synonymous-codon	USP32	GRCh38.p7	17:60181480	CACTCCTCAGGACCA[C/T]GAGGTAGCTTTGGCC	84669
rs3207630	snp	C/G	0	0	missense	USP32	GRCh38.p7	17:60181466	ATGAGGTAGCTTTGG[C/G]CAATGGATTCCTTTA	84669
rs3214969	in-del	-/C	0.000545757	0.01651	intron-variant	USP32	GRCh38.p7	17:60222360	AAAAGTAACAGAAGA[-/C]CCCCATCTATGACTG	84669
rs3220244	microsatellite	(CA)20/21/22/23	0.45701	0.270836	intron-variant	USP32	GRCh38.p7	17:60291570	GTTTTTGTGTTTATA[(CA)20/21/22/23]AGAGAGAGAAGCACT	84669

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