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
rs1538562	snp	A/G	0.0279526	0.114869	intron-variant	FAM188A	GRCh38.p7	10:15840376	TAATTTTGAACATTT[A/G]AACAGCTATATGATG	80013
rs2297882	snp	A/G	0.456814	0.140456	utr-variant-5-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860304	AGTTCGGACATGATG[A/G]GGAACCGGCGGGCGG	80013
rs2883452	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15859392	TAACCTCATCATCAT[C/T]TTTCCTAAGTCACCT	80013
rs4266971	snp	C/T	0.216349	0.247725	intron-variant	FAM188A	GRCh38.p7	10:15801062	taacaggagaagcag[C/T]ttctgctaacaaaga	80013
rs4387254	snp	C/G	0.479258	0.0997024	intron-variant	FAM188A	GRCh38.p7	10:15808184	TTGTTATTTTAAGGT[C/G]TTAAAAGTCACAGAA	80013
rs4442439	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15797384	CATTTACCATCCCTT[C/G]CTAGAAACTTCTTAG	80013
rs4584469	snp	C/G/T			intron-variant	FAM188A	GRCh38.p7	10:15790455	GAGAATAAAGACGAC[C/G/T]TTGGTTGAAGGCACT	80013
rs4748207	snp	G/T	0.0182019	0.0936463	intron-variant	FAM188A	GRCh38.p7	10:15787609	TGTGAGGGTAAGCTA[G/T]GTTTTAAGGTTTATG	80013
rs6602058	snp	A/G	0.451359	0.148171	intron-variant	FAM188A	GRCh38.p7	10:15845984	cctgccactacaccc[A/G]gctaatttttgtatt	80013
rs6602059	snp	C/G	0.249603	0.25	intron-variant	FAM188A	GRCh38.p7	10:15848339	ATTCTATAAGCTAAT[C/G]ATTACATGGCATTgg	80013
rs6602061	snp	C/G	0.306679	0.24349	intron-variant	FAM188A	GRCh38.p7	10:15855395	AGCATTACTTTTCTT[C/G]TCAAGAGTTCTCATA	80013
rs7069213	snp	G/T	0.0345262	0.126772	intron-variant	FAM188A	GRCh38.p7	10:15833999	AAGTTACTTAATATT[G/T]ACAATCtttaaaaat	80013
rs7069225	snp	G/T	0.040671	0.13668	intron-variant	FAM188A	GRCh38.p7	10:15842938	aaGACTGTTCTTTAT[G/T]GCATGCTGCCACCTA	80013
rs7070324	snp	C/T	0.0437281	0.141251	intron-variant	FAM188A	GRCh38.p7	10:15851542	TGGAAAACTCAAACT[C/T]ACCTATAGGTTTCAC	80013
rs7072209	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15848663	aaaaaaaaaaaaaaa[A/G]AAAGAAAAATTAAAT	80013
rs7072213	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15848667	aaaaaaaaaaaGaaa[A/G]AAAAATTAAATGGCA	80013
rs7072683	snp	A/G	0.0119152	0.0762602	intron-variant	FAM188A	GRCh38.p7	10:15843294	ACAATTAAAGCAATA[A/G]TTAGTGAAATGCATT	80013
rs7075115	snp	A/C	0	0	intron-variant	FAM188A	GRCh38.p7	10:15801648	agtagtctgcagaaa[A/C]gatgatatggttatt	80013
rs7081355	snp	A/G	0.239326	0.249772	intron-variant	FAM188A	GRCh38.p7	10:15850332	aacaggatggctgca[A/G]tgttcagggaacaag	80013
rs7086658	snp	A/C	0.209997	0.246779	intron-variant	FAM188A	GRCh38.p7	10:15851907	TCTGTTTACACTTAC[A/C]ATCATTATCTACTGT	80013
rs7090975	snp	A/C	0.289683	0.24683	intron-variant	FAM188A	GRCh38.p7	10:15845370	TTACACAGTATCATG[A/C]TCTAATTTTTATACT	80013
rs7091401	snp	A/C	0.209997	0.246779	intron-variant	FAM188A	GRCh38.p7	10:15845588	cactgcagccctgaa[A/C]tcctgagctcaaaga	80013
rs7094427	snp	G/T	0.232067	0.249356	intron-variant	FAM188A	GRCh38.p7	10:15849447	ATATCATCTTACTGG[G/T]TTTTTTTTTTTTTCT	80013
rs7096756	snp	A/C	0.0463947	0.145069	intron-variant	FAM188A	GRCh38.p7	10:15847073	CCACATTAAATATAT[A/C]TATTTTCAAAACACG	80013
rs7097118	snp	A/C	0.130013	0.219324	intron-variant	FAM188A	GRCh38.p7	10:15841378	TCAATAGATTCATTA[A/C]AACAAAGGAACAAGA	80013
rs7097989	snp	A/G	0.260504	0.249779	intron-variant	FAM188A	GRCh38.p7	10:15841981	CCTGTTGAAACCTCT[A/G]TTTTTTTTCCCTCAC	80013
rs7100782	snp	A/G	0.0383715	0.133092	intron-variant	FAM188A	GRCh38.p7	10:15847374	GAAATCAGTTGTTAC[A/G]AATTTTATTCAGAAA	80013
rs7342102	snp	A/G	0.285519	0.247464	intron-variant	FAM188A	GRCh38.p7	10:15840921	TGAAAAACTTAAGGC[A/G]TAATTAAAATTGCCT	80013
rs7476607	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15856492	TAGTCTTTAGGAGAA[A/C]CAATAAAATAACTGG	80013
rs7895562	snp	C/G	0.00159617	0.0282053	utr-variant-5-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860506	TTTTCCGTACCGGAA[C/G]TGCTGGTGCCACTTC	80013
rs7896076	snp	A/G	0.231189	0.249291	intron-variant	FAM188A	GRCh38.p7	10:15830828	ATATTTTAGCGATGC[A/G]GGCAAGGAAATTCTG	80013
rs7898385	snp	C/T	0.0704125	0.17392	intron-variant	FAM188A	GRCh38.p7	10:15857356	ccccacccagaaCTC[C/T]GTATTTCCTCATCTT	80013
rs7903095	snp	A/G	0.231482	0.249313	intron-variant	FAM188A	GRCh38.p7	10:15837442	GGAAAGTTTTGGGAC[A/G]TTTCTAAATTTTTCA	80013
rs7904049	snp	A/G	0.0696718	0.173152	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862292	AGCAAGTGAGAGATC[A/G]GGGAAGTAGTACTGA	80013
rs7904872	snp	G/T	0.321769	0.239477	intron-variant	FAM188A	GRCh38.p7	10:15795432	CTACAAGGACTTCAC[G/T]GATACAGCAACTTCC	80013
rs7905215	snp	C/G/T	0.0722113	0.178567	intron-variant	FAM188A	GRCh38.p7	10:15795878	CAGAGGGGTCAACTA[C/G/T]ACCTTCAGTACTCCA	80013
rs7909265	snp	C/T	0.0383715	0.133092	intron-variant	FAM188A	GRCh38.p7	10:15789897	GCTGATGATGACTAC[C/T]TTATGGAAAATGGTC	80013
rs7910149	snp	C/T	0.0376037	0.131863	intron-variant	FAM188A	GRCh38.p7	10:15793706	GCTCTGGAGAAGTGA[C/T]TCAAACCATCAAAAG	80013
rs7912258	snp	C/T	0.32153	0.239548	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782093	AATCGAACGTTGTTA[C/T]ATACTCACATAATTA	80013
rs7913602	snp	C/T	0.255503	0.249939	intron-variant	FAM188A	GRCh38.p7	10:15848582	gagcttgcactgagc[C/T]gagattgtgccactg	80013
rs7913650	snp	C/T	0.0700422	0.173537	intron-variant	FAM188A	GRCh38.p7	10:15857717	CCGCATTTTTTAAAA[C/T]GAACAGGGATTTGTA	80013
rs7920842	snp	G/T	0.288906	0.246954	intron-variant	FAM188A	GRCh38.p7	10:15832518	TGAAGAATAGGATGA[G/T]CTCAATTAAAGAGAG	80013
rs7923528	snp	C/T	0.427271	0.176281	intron-variant	FAM188A	GRCh38.p7	10:15847373	TGAAATCAGTTGTTA[C/T]GAATTTTATTCAGAA	80013
rs7923731	snp	C/T	0.0766824	0.180169	intron-variant	FAM188A	GRCh38.p7	10:15789756	TTCTTGAAGGAATGT[C/T]AGTGATCCACTGATA	80013
rs9783219	snp	C/T	0.110167	0.207236	intron-variant	FAM188A	GRCh38.p7	10:15799054	atgttttgcagggca[C/T]atggtcttagcagca	80013
rs10508494	snp	C/G	0.467946	0.122472	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779779	GAAAAGTAAAAGAGA[C/G]GTTGAAAGATCAAAC	80013
rs10508495	snp	A/T	0.232067	0.249356	intron-variant	FAM188A	GRCh38.p7	10:15811762	CACTTTCTCCTTATT[A/T]CTAGGGTCTAATACA	80013
rs10690053	in-del	-/CA	0.0333695	0.124785	intron-variant	FAM188A	GRCh38.p7	10:15795004	AAAGTCATTCACTCC[-/CA]GTTTCAACTGTGGTT	80013
rs10716234	in-del	-/T			intron-variant	FAM188A	GRCh38.p7	10:15831693	TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCGC	80013
rs10719399	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15848634	GCTAGACTTCATCTC[-/A]AAAAAAAAAAAAAAA	80013
rs10795321	snp	C/G	0.461703	0.132974	intron-variant	FAM188A	GRCh38.p7	10:15819276	TTCCTCCAAGCATCT[C/G]ATAGAAAGTAAATGT	80013
rs10795322	snp	A/G	0.242775	0.249896	intron-variant	FAM188A	GRCh38.p7	10:15819577	tccacaggggagctc[A/G]ggcaatctagctgac	80013
rs10904626	snp	C/T	0.316243	0.241064	intron-variant	FAM188A	GRCh38.p7	10:15801332	CTGCTAAACCCAAGC[C/T]TTGAAGGGAAAAGAT	80013
rs10904627	snp	A/G	0.273049	0.248935	intron-variant	FAM188A	GRCh38.p7	10:15801463	AGTACCCTGCCAGTA[A/G]GAGACCACCTTTTAA	80013
rs10904628	snp	G/T	0.219049	0.248077	intron-variant	FAM188A	GRCh38.p7	10:15809318	GCCTTCATCTAATAA[G/T]AGCTAGTTTTTTCTT	80013
rs10904629	snp	C/T	0.456332	0.141164	intron-variant	FAM188A	GRCh38.p7	10:15812753	TACGTGATGTGCATA[C/T]AGTGAACAAATTGCT	80013
rs10904630	snp	C/T	0.29789	0.24537	intron-variant	FAM188A	GRCh38.p7	10:15816561	TTCAATTGTTTTCTC[C/T]ATAACACAAGTGATT	80013
rs10904631	snp	A/C	0.222035	0.248431	intron-variant	FAM188A	GRCh38.p7	10:15826013	gacaaaaataatgta[A/C]aaataCTGAAGAATT	80013
rs10904632	snp	C/T	0.437259	0.165632	intron-variant	FAM188A	GRCh38.p7	10:15844627	ACATATAAGCTCCTT[C/T]TTAAATACAACTTTT	80013
rs11253647	snp	C/G	0.2768	0.248559	intron-variant	FAM188A	GRCh38.p7	10:15787493	TCAGGTGGTTCTAGT[C/G]AACCACCTTCCTCAG	80013
rs11253649	snp	A/G	0.00795532	0.062565	intron-variant	FAM188A	GRCh38.p7	10:15793284	TTAAGCTGAGTAAGT[A/G]TGCTAGTCTCCCCTT	80013
rs11253650	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15797914	ATTTCTAACACATTT[C/T]TCTTTTTCAATTGTC	80013
rs11253651	snp	A/T	0.455977	0.141681	intron-variant	FAM188A	GRCh38.p7	10:15803421	ACATTCAATTGAGAG[A/T]GTTTTACAATCAAGA	80013
rs11253655	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15809617	AGGTCCATTTACGTA[C/G]TGCATTTCACCTCAC	80013
rs11253656	snp	A/T	0.235564	0.249583	intron-variant	FAM188A	GRCh38.p7	10:15816621	AAGAAAGAAGAAGAA[A/T]TTATAACTAAATCAT	80013
rs11253658	snp	A/G	0	0	intron-variant	FAM188A	GRCh38.p7	10:15824865	GTAAACACATGCTTA[A/G]ACATCTAGTCTGGAT	80013
rs11253659	snp	A/T	0.0524604	0.153226	intron-variant	FAM188A	GRCh38.p7	10:15833426	CACTAAAGTCATACA[A/T]TTGGGATTTGAACCC	80013
rs11253660	snp	A/G	0.242201	0.249878	intron-variant	FAM188A	GRCh38.p7	10:15845295	TCCTGGTAAATTGTG[A/G]CAGGTAATGAGGTCT	80013
rs11253661	snp	C/T	0.241914	0.249869	intron-variant	FAM188A	GRCh38.p7	10:15845325	TATGATTGTATTATG[C/T]ATTTGGTTCCATTAT	80013
rs11327084	in-del	-/A	0.0788843	0.182262	intron-variant	FAM188A	GRCh38.p7	10:15789399	TGATCAGGTTCCAGG[-/A]AAAAAAAATCGCATA	80013
rs11385214	in-del	-/T			intron-variant	FAM188A	GRCh38.p7	10:15846741	TTTTTTTTTTTTTTT[-/T]GAGACAAAGTCTCGC	80013
rs11410031	in-del	-/T	0	0	intron-variant	FAM188A	GRCh38.p7	10:15832457	GACACTGAAATGAGA[-/T]TTTTTTTTTTCATTG	80013
rs11423907	in-del	-/T	0.287867	0.247116	intron-variant	FAM188A	GRCh38.p7	10:15834973	TGTTAAGGCAACTGA[-/T]TTTTTTTAGATCATG	80013
rs11455489	in-del	-/T			intron-variant	FAM188A	GRCh38.p7	10:15846725	CAGTTTAGGAATGCA[-/T]TTTTTTTTTTTTTTT	80013
rs11455843	in-del	-/T			intron-variant	FAM188A	GRCh38.p7	10:15800231	GTAGATACTAGTCTA[-/T]TTTTTTCTACTACCA	80013
rs11597852	snp	G/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784565	gcctgaccaacaagg[G/T]gaaaccccatctcta	80013
rs11813064	snp	A/G	0.0248432	0.108648	intron-variant	FAM188A	GRCh38.p7	10:15791677	TTTTACCAGTTGAAT[A/G]TCCAGATTGCTAAAA	80013
rs11813535	snp	C/T	0.271162	0.249103	intron-variant	FAM188A	GRCh38.p7	10:15816380	TAAAATTGTGGGAAG[C/T]ATTCCATCTTAAAAG	80013
rs11818243	snp	A/G	0.339429	0.233457	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782086	GTACGGGAATCGAAC[A/G]TTGTTACATACTCAC	80013
rs12218978	snp	C/T	0.31503	0.241394	intron-variant	FAM188A	GRCh38.p7	10:15853957	gcttacagattgttc[C/T]gatgacatcactggt	80013
rs12221218	snp	C/T	0.292008	0.246445	intron-variant	FAM188A	GRCh38.p7	10:15802401	GAGAAGCAAGCACCT[C/T]CTTCACAAGGCAGCA	80013
rs12242143	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15848631	agagctagacttcat[C/T]tcaaaaaaaaaaaaa	80013
rs12243247	snp	A/G	0.238171	0.24972	intron-variant	FAM188A	GRCh38.p7	10:15831339	ATGTGTTATCCAGGA[A/G]AAACCAAGAAGGTTC	80013
rs12243475	snp	A/T	0.186105	0.241697	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861844	tattttaattaattt[A/T]attttatttCTTCAG	80013
rs12247946	snp	C/T	0.156319	0.231784	intron-variant	FAM188A	GRCh38.p7	10:15856850	TGTGGTCACtctgtc[C/T]gcttcttaccatctc	80013
rs12247963	snp	A/G	0.338296	0.233889	intron-variant	FAM188A	GRCh38.p7	10:15793250	GAACACTTTGAATAG[A/G]CCTGATAACTGCTTC	80013
rs12257572	snp	A/C	0.289683	0.24683	intron-variant	FAM188A	GRCh38.p7	10:15843864	CACAGTGAAGTGTCT[A/C]Cttctcaaagtgtag	80013
rs12258622	snp	C/T	0.308166	0.243139	intron-variant	FAM188A	GRCh38.p7	10:15823077	GAATATTAACTCTGT[C/T]ATTTTTGTGGCCAAC	80013
rs12262809	snp	A/G	0.478603	0.101197	intron-variant	FAM188A	GRCh38.p7	10:15793278	TTCTCTTTAAGCTGA[A/G]TAAGTGTGCTAGTCT	80013
rs12264533	snp	A/G	0.437259	0.165632	intron-variant	FAM188A	GRCh38.p7	10:15827591	aAGCCTTGGATATAA[A/G]AAAATATATCATTAA	80013
rs12265790	snp	C/T	0.261332	0.249743	intron-variant	FAM188A	GRCh38.p7	10:15831289	TTTCTTTTCTAGCAA[C/T]AATCAGCCTGGCAGT	80013
rs12354532	snp	C/G	0	0	intron-variant	FAM188A	GRCh38.p7	10:15812555	TGACAGCTCTCACTA[C/G]TGCTAAATTTAAATT	80013
rs12572784	snp	A/G	0.0944967	0.195752	intron-variant	FAM188A	GRCh38.p7	10:15803314	GGTTCCTAGTATAAA[A/G]ATCTGTAGACTAATC	80013
rs12764431	snp	G/T	0	0	intron-variant	FAM188A	GRCh38.p7	10:15821293	AAGTATTACCAGTTG[G/T]TTTAGTGAAGCATAT	80013
rs12768419	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15843363	GAAAAAATAATGTGT[A/G]CTCCCTTTCTAATCT	80013
rs12769648	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15852318	TTGTTTCTAGGAATA[C/T]CAAGTTCAGTCTCAA	80013
rs12769938	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15843345	TCTTCAATTTTAAAG[A/T]GGGAAAAAATAATGT	80013
rs12770143	snp	A/T	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15843435	ATTTGACAGGAACTG[A/T]GCAGTTATTTATTCA	80013
rs12770144	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15843440	ACAGGAACTGTGCAG[C/T]TATTTATTCAGAGTA	80013
rs12781122	snp	C/T	0	0	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15841587	TGACAAAGGAGTTCC[C/T]TCTGCTCTTCCTCTA	80013

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