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
rs8593	snp	C/T	0.02016	0.0983543	utr-variant-3-prime	MAP3K9	GRCh38.p7	14:70722705	AGCCAAAGGAAAGAA[C/T]CTGGTAAGTTTCCTT	4293
rs36278	snp	C/T			upstream-variant-2KB, intron-variant	MAP3K9, LOC100506411	GRCh38.p7	14:70809457	GGCTGCGCGAGCAGG[C/T]ACCGGCGGCAGAGGT	4293
rs36279	snp	A/C			upstream-variant-2KB, intron-variant	MAP3K9, LOC100506411	GRCh38.p7	14:70809428	GTGACGAGGCCGCCC[A/C]CGGGGGGGCGAGCGG	4293
rs36280	snp	A/G			missense, upstream-variant-2KB	MAP3K9, LOC100506411	GRCh38.p7	14:70809093	GAGGATGGAGCAggg[A/G]ccggggccgaggagg	4293
rs731571	snp	A/G	0.368938	0.219895	intron-variant	MAP3K9	GRCh38.p7	14:70804632	TGTGTGTTTACAACT[A/G]TGCTTAAGACTGGAG	4293
rs740034	snp	A/G	0.0275645	0.114116	upstream-variant-2KB, intron-variant	MAP3K9, LOC100506411	GRCh38.p7	14:70809635	CAATGGGAAGGCAgc[A/G]ggcgcggggcggggc	4293
rs740035	snp	C/T	0.00874735	0.0655527	upstream-variant-2KB, intron-variant	MAP3K9, LOC100506411	GRCh38.p7	14:70809545	GGTGGTCCCGGCGAG[C/T]TGGCGGTGCGGGGGG	4293
rs740036	snp	G/T	0.5	0	upstream-variant-2KB, intron-variant	MAP3K9, LOC100506411	GRCh38.p7	14:70809489	agagcggcggccggc[G/T]ggcagcggcgggCAC	4293
rs886600	snp	C/G	0.491051	0.0662916	intron-variant	MAP3K9	GRCh38.p7	14:70762564	TGGGCAAAGGATTGA[C/G]TGGACATTTCTCCAA	4293
rs1034769	snp	G/T	0.266819	0.249434	intron-variant	MAP3K9	GRCh38.p7	14:70787981	TCCCAATAGAATTCT[G/T]GACAGCAGAGGTGTT	4293
rs1160880	in-del	-/TAGA	0.222928	0.24853	intron-variant	MAP3K9	GRCh38.p7	14:70751059	CTTTTCCATTTGAAT[-/TAGA]TAGAGATCTCCGTTA	4293
rs1476609	snp	C/T	0.282632	0.247861	intron-variant, upstream-variant-2KB	MAP3K9	GRCh38.p7	14:70755348	ACCATCTGTATGGTC[C/T]TGTTCCTGCACTTAA	4293
rs1476610	snp	A/C	0.239037	0.24976	intron-variant	MAP3K9	GRCh38.p7	14:70731038	TACAGGGATCATGGC[A/C]TTCTAGGTCACTACT	4293
rs1548584	snp	A/G	0.345704	0.230956	intron-variant	MAP3K9	GRCh38.p7	14:70767947	CAGGCACAGTGGCTC[A/G]CTTCTGTAATTCCAG	4293
rs1548585	snp	A/G	0.493386	0.0571263	intron-variant	MAP3K9	GRCh38.p7	14:70767879	aggcgttcaagacca[A/G]ccggtcaatacaaaa	4293
rs1801670	snp	C/T			utr-variant-3-prime	MAP3K9	GRCh38.p7	14:70722676	CTTTTTTTTTTTTTT[C/T]TTTCGAGGTACTGTA	4293
rs1859465	snp	A/G	0.107694	0.205546	intron-variant	MAP3K9	GRCh38.p7	14:70736514	TGAGTCTTAGTTCCT[A/G]TTGAAGAAATAAAAG	4293
rs1987652	snp	A/G	0.401392	0.198948	intron-variant	MAP3K9	GRCh38.p7	14:70787398	GCCTCAGCCTCCCGA[A/G]TAGCTAGGATTACAG	4293
rs1990032	snp	C/G	0.017647	0.0922621	synonymous-codon	MAP3K9	GRCh38.p7	14:70742562	GGAGGAGGAGCTGAC[C/G]CGGGCTGCACTGCAG	4293
rs2023954	snp	C/T	0.351635	0.228408	intron-variant	MAP3K9	GRCh38.p7	14:70804659	GCATTTAAATGAATA[C/T]TTAACACCTACTGTG	4293
rs2023955	snp	A/C	0.158632	0.232706	intron-variant	MAP3K9	GRCh38.p7	14:70804338	GCACAAGTTAGTAAT[A/C]AGTCTGGATTCATTC	4293
rs2051857	snp	A/G	0.0898077	0.191933	intron-variant	MAP3K9	GRCh38.p7	14:70796710	GAAGGATGAGGGGAA[A/G]CAGAAGCACAGAAAA	4293
rs2107665	snp	A/G	0.157642	0.232314	intron-variant	MAP3K9	GRCh38.p7	14:70792955	TTGCACCTTGTCCTC[A/G]TCTCCAACCTTCTCT	4293
rs2107666	snp	C/G	0.227074	0.248947	intron-variant	MAP3K9	GRCh38.p7	14:70780190	CACATTATGAGGAAG[C/G]CTGGTGCTTTGGGTT	4293
rs2158529	snp	A/C	0.488606	0.0746142	intron-variant	MAP3K9	GRCh38.p7	14:70793164	AGGAGCTGCTGGAGC[A/C]GACCACTGCCCGGTG	4293
rs2158530	snp	A/G	0.403684	0.197183	intron-variant	MAP3K9	GRCh38.p7	14:70780278	ATCATGTCTCCTTCT[A/G]TCCTCCAGCCCAACA	4293
rs2158531	snp	A/G	0.403334	0.197456	intron-variant	MAP3K9	GRCh38.p7	14:70780251	AACAAGGCAGCAGAA[A/G]TCCACACCTCATGCT	4293
rs2269946	snp	A/G	0.0901694	0.192235	intron-variant	MAP3K9	GRCh38.p7	14:70746097	TTAACAGCAAAATCA[A/G]CCAACCAGGAATATT	4293
rs2286052	snp	C/T	0.0901694	0.192235	intron-variant	MAP3K9	GRCh38.p7	14:70740377	GATGAAGTTCACTTG[C/T]ACAGTGAATTTTCCA	4293
rs2286053	snp	A/G	0.0941369	0.195465	utr-variant-3-prime	MAP3K9	GRCh38.p7	14:70729710	TGCCTCAGTGAGAAC[A/G]GGGGGACGGGGATGT	4293
rs2286054	snp	A/G	0.0103295	0.0711199	utr-variant-3-prime	MAP3K9	GRCh38.p7	14:70729670	TACAGTAAAGTTGCA[A/G]TGAAGAGGTTCATGA	4293
rs2301884	snp	G/T			utr-variant-3-prime	MAP3K9	GRCh38.p7	14:70722704	AGGAAACTTACCAGG[G/T]TCTTTCCTTTGGCTT	4293
rs2301885	snp	C/T			utr-variant-3-prime	MAP3K9	GRCh38.p7	14:70722703	GGAAACTTACCAGGT[C/T]CTTTCCTTTGGCTTT	4293
rs2332455	snp	C/T	0.235854	0.249599	intron-variant	MAP3K9	GRCh38.p7	14:70747154	GTCATTTGTGTAGAA[C/T]AAAAATGACACTTGA	4293
rs2332456	snp	A/G	0.046775	0.145601	intron-variant	MAP3K9	GRCh38.p7	14:70748514	GTATCCCTATATCAA[A/G]TTAACCTTCTTCTAG	4293
rs2332457	snp	G/T	0.491629	0.0641526	intron-variant	MAP3K9	GRCh38.p7	14:70748663	CCAACTGCATTCTTC[G/T]CTGGTTTGGACAATT	4293
rs2332458	snp	C/T	0.222333	0.248464	intron-variant	MAP3K9	GRCh38.p7	14:70766941	ATGCACTTCTAATCA[C/T]TCCTGACTGCTGCAT	4293
rs2877693	snp	C/T	0.0685596	0.171987	intron-variant, upstream-variant-2KB	MAP3K9	GRCh38.p7	14:70755726	GAAAGGCCCATTTAA[C/T]GGGTTATAAATTGTG	4293
rs3081458	in-del	-/TA			intron-variant	MAP3K9	GRCh38.p7	14:70742937	atatatatatatata[-/TA]GGTTTGAATAGAAAA	4293
rs3081478	in-del	-/TAATACCT	0.493432	0.0569306	intron-variant	MAP3K9	GRCh38.p7	14:70763483	CCATACATAATACCT[-/TAATACCT]GATAATGCTAATAAG	4293
rs3081535	in-del	-/AA	0.347694	0.230122	intron-variant	MAP3K9	GRCh38.p7	14:70804693	AGGGATTGAAAAAAT[-/AA]ATGCAGGGAGGTTTA	4293
rs3742847	snp	G/T	0.288573	0.251354	upstream-variant-2KB, nc-transcript-variant	MAP3K9, LOC100506411	GRCh38.p7	14:70809269	CGGCCGCCGTCGTTG[G/T]GGGGGGGTCCTCCCA	4293
rs3742848	snp	A/G	0.493013	0.058691	utr-variant-3-prime	MAP3K9	GRCh38.p7	14:70724706	GGTTTCAGAAATAGT[A/G]TGCTGCCTGTTCCTG	4293
rs3814872	snp	G/T	0.189667	0.242622	intron-variant	MAP3K9	GRCh38.p7	14:70761196	GTTTCTTCTGTATTC[G/T]TTTCCTTGCCTAGTA	4293
rs3814873	snp	A/T			synonymous-codon	MAP3K9	GRCh38.p7	14:70733113	CCGCTGCGAGGTGGC[A/T]CTGCTCGGCTGTGGG	4293
rs3814874	snp	A/G	0.00213003	0.032565	missense	MAP3K9	GRCh38.p7	14:70733094	CTCGGCTGTGGGGCT[A/G]TTCTGGCAGCCACAG	4293
rs3829955	snp	C/T	0.364117	0.222435	synonymous-codon	MAP3K9	GRCh38.p7	14:70732735	TCCATGTACCCACAA[C/T]CCCCTGGTCAATGTC	4293
rs4141095	snp	A/G	0.19853	0.244644	intron-variant	MAP3K9	GRCh38.p7	14:70735933	TTCACCCTTTCACCA[A/G]CTGTCCTGGTAACAA	4293
rs4528504	snp	A/G	0.157642	0.232314	intron-variant	MAP3K9	GRCh38.p7	14:70794913	CGATCTCCTGACCTC[A/G]TGATCCACCTGTCTC	4293
rs4899367	snp	C/T	0.180702	0.240204	intron-variant	MAP3K9	GRCh38.p7	14:70735087	TGTGGGACAGACCTA[C/T]GTGGGTAGTGCACAG	4293
rs4899368	snp	A/G	0.22263	0.248497	intron-variant	MAP3K9	GRCh38.p7	14:70742279	CAAGCTCAGTCCCGG[A/G]CTCCCTCAAACCCTC	4293
rs4899369	snp	A/T	0.222035	0.248431	intron-variant	MAP3K9	GRCh38.p7	14:70748121	AAAAAAAAAAAAAAA[A/T]GGTAAAAGAAATTAA	4293
rs4899370	snp	A/G	0.278664	0.248351	intron-variant	MAP3K9	GRCh38.p7	14:70748123	AAAAAAAAAAAAATG[A/G]TAAAAGAAATTAACC	4293
rs4899371	snp	A/G	0.479095	0.100076	intron-variant	MAP3K9	GRCh38.p7	14:70802394	CTTCCCAAATCCAGA[A/G]TTTGAACCTAAGGTA	4293
rs4902843	snp	A/C	0.433938	0.169313	intron-variant	MAP3K9	GRCh38.p7	14:70742308	TCTGCCACACGAGTT[A/C]TTTGCCCTGCTCCCA	4293
rs4902844	snp	C/T	0.235564	0.249583	intron-variant	MAP3K9	GRCh38.p7	14:70745669	CTTGAACCCGGGAGG[C/T]GGAGGTTGCAGTGAG	4293
rs4902845	snp	C/T	0.231775	0.249335	intron-variant	MAP3K9	GRCh38.p7	14:70748063	AGTGAGCTGAGATCG[C/T]GCCACTGCACTTCAG	4293
rs4902846	snp	A/G	0.344592	0.231414	intron-variant	MAP3K9	GRCh38.p7	14:70752493	ACTATTACACTTCCT[A/G]ACAAACCTTTCATGT	4293
rs4902847	snp	A/G	0.497984	0.0316851	intron-variant, utr-variant-5-prime	MAP3K9	GRCh38.p7	14:70753320	ACAGTGTTGGTGAGA[A/G]CTTTGCTGAGGGACA	4293
rs4902848	snp	A/G	0.495634	0.0465208	intron-variant, utr-variant-5-prime	MAP3K9	GRCh38.p7	14:70753499	GAAATACAAGTTTAC[A/G]TGGATCTGAGCTCAG	4293
rs4902849	snp	A/T	0.418169	0.184985	intron-variant	MAP3K9	GRCh38.p7	14:70765015	TTACAGTAAGCTAAG[A/T]TTAATTTATTATTGA	4293
rs4902852	snp	C/T	0.22263	0.248497	intron-variant	MAP3K9	GRCh38.p7	14:70766199	CTAGGTTCACTGTAA[C/T]AAGAGTCAGTATGGA	4293
rs4902854	snp	C/T	0.496348	0.0425753	intron-variant	MAP3K9	GRCh38.p7	14:70781674	AAGGGTTTACACACA[C/T]AACTTCATTTAATCC	4293
rs4902855	snp	C/T	0.490508	0.0682328	intron-variant	MAP3K9	GRCh38.p7	14:70788237	AGAATATGACTAAAA[C/T]AATGAAAATGCAAGT	4293
rs4902856	snp	A/G	0.459914	0.13578	intron-variant	MAP3K9	GRCh38.p7	14:70797407	CAAAGCAAGACTCCC[A/G]TCTCTATTAAAATAA	4293
rs4902857	snp	C/T	0.349344	0.229414	intron-variant	MAP3K9	GRCh38.p7	14:70800628	GGGATACAACTGCAA[C/T]TGCTCTGAGCCCCTC	4293
rs4902858	snp	A/G	0.366473	0.221211	intron-variant	MAP3K9	GRCh38.p7	14:70806075	AACGTCACAACACAT[A/G]CTCAGAGGAGAAGTT	4293
rs4902859	snp	C/T	0.345037	0.231231	intron-variant	MAP3K9	GRCh38.p7	14:70806108	AAAGGGTAACTCTGG[C/T]GATGAAGTGTCAGTG	4293
rs5809495	in-del	-/T	0.0851086	0.187921	intron-variant	MAP3K9	GRCh38.p7	14:70748809	TTTGTTGTTTTTTTT[-/T]GTTTTGTTTACCTTT	4293
rs6573977	snp	A/G	0.492237	0.0618148	downstream-variant-500B	MAP3K9	GRCh38.p7	14:70722480	AAAAAAAAAGAAAAA[A/G]AAGGGGGAAAGGATG	4293
rs6573978	snp	C/T	0.239326	0.249772	intron-variant	MAP3K9	GRCh38.p7	14:70734215	ATACCGGCCCCTTAA[C/T]ACAAGTGTAGTATGA	4293
rs6573979	snp	C/T	0.49168	0.063958	intron-variant	MAP3K9	GRCh38.p7	14:70757503	tacaaagctacagat[C/T]tgatgcaattcctat	4293
rs6573980	snp	A/G	0.222928	0.24853	intron-variant	MAP3K9	GRCh38.p7	14:70757808	tcgatgggaaaaaat[A/G]gtcttttcaataaat	4293
rs6573981	snp	C/T	0.222035	0.248431	intron-variant	MAP3K9	GRCh38.p7	14:70765687	ggcttccctgggcca[C/T]attggaagaaatgtc	4293
rs7140653	snp	C/T	0.227074	0.248947	intron-variant	MAP3K9	GRCh38.p7	14:70779165	GGGAGAAGAAGGAGC[C/T]GCAGTGAAGGGCTGG	4293
rs7146255	snp	C/T	0.0437281	0.141251	intron-variant	MAP3K9	GRCh38.p7	14:70788426	taatcctcacttcta[C/T]cccgtaagatgagat	4293
rs7147731	snp	A/T	0.496245	0.0431677	intron-variant	MAP3K9	GRCh38.p7	14:70758382	taataactttttttt[A/T]aaaaaaaggcaataa	4293
rs7150824	snp	A/G/T	0.000399281	0.0141238	intron-variant	MAP3K9	GRCh38.p7	14:70801617	GAAGCACCCAACTCA[A/G/T]TGCCAAGGCAGACAC	4293
rs7151024	snp	A/C/G	0.313957	0.242645	intron-variant	MAP3K9	GRCh38.p7	14:70801729	GCACAGAGCACTAAG[A/C/G]GGGTGAGTGGGGAAA	4293
rs7151405	snp	C/T	0.497959	0.0318836	intron-variant	MAP3K9	GRCh38.p7	14:70771969	CAGGGAGCCAGAGTG[C/T]GGCCGCTGTGCATCC	4293
rs7152516	snp	G/T	0.222035	0.248431	intron-variant	MAP3K9	GRCh38.p7	14:70771887	CTCAGACCCAACACA[G/T]AGCAGGCTCCCTGTT	4293
rs7153601	snp	C/T	0.308041	0.243169	synonymous-codon	MAP3K9	GRCh38.p7	14:70738256	TTACCCTTCATCTCC[C/T]GAGGCAAGCTCCTTC	4293
rs7154907	snp	C/G	0.498034	0.0312882	intron-variant	MAP3K9	GRCh38.p7	14:70769066	CAAATGTATATATGG[C/G]TGGGAGTGGTGGAGC	4293
rs7155910	snp	G/T	0.171057	0.237209	intron-variant, upstream-variant-2KB	MAP3K9, LOC100506411	GRCh38.p7	14:70807960	TTGACCAGTTCCAAA[G/T]ATAGGCAAGGATCTA	4293
rs7156271	snp	A/G	0.493013	0.058691	utr-variant-3-prime	MAP3K9	GRCh38.p7	14:70726586	GCATCAGACAAGTTA[A/G]GTGGGGGAATTAGGA	4293
rs7156877	snp	G/T	0.0119091	0.0762411	intron-variant, upstream-variant-2KB	MAP3K9, LOC100506411	GRCh38.p7	14:70807972	AAAGATAGGCAAGGA[G/T]CTAGAATGAGAAGAA	4293
rs7157496	snp	A/C	0.5	0	intron-variant	MAP3K9	GRCh38.p7	14:70765754	aaaaaaaaaaaacaa[A/C]aaaaaacaaaaaaaa	4293
rs7159957	snp	C/G/T	0.039522	0.134904	intron-variant, utr-variant-5-prime	MAP3K9	GRCh38.p7	14:70753782	TAATTAACCACCTCC[C/G/T]GAGGCTTGGTAATCC	4293
rs7160912	snp	A/C	0.498503	0.0273153	intron-variant	MAP3K9	GRCh38.p7	14:70770011	CCCAAAGGGAATAAG[A/C]TAAACAGAGTCTCTG	4293
rs7161415	snp	C/T	0.490727	0.0674567	intron-variant, utr-variant-5-prime	MAP3K9	GRCh38.p7	14:70753906	GGCACAGCAACTCCA[C/T]GCCTGTGCTGGGCCA	4293
rs8005459	snp	C/G	0.49334	0.057322	intron-variant	MAP3K9	GRCh38.p7	14:70767099	TTTGAAAGAACTCAT[C/G]CCGGCTGGGTGCGGT	4293
rs8006424	snp	A/G	0.178144	0.239451	utr-variant-3-prime	MAP3K9	GRCh38.p7	14:70723199	GAGACACAAGCTACA[A/G]TAAGGCTTCCAAGCT	4293
rs8006539	snp	G/T	0.445328	0.156035	utr-variant-3-prime	MAP3K9	GRCh38.p7	14:70723037	AGATATCTGGGTTTC[G/T]GTGGGGAGTGCAGGA	4293
rs8006715	snp	A/G	0.345704	0.230956	intron-variant, upstream-variant-2KB	MAP3K9	GRCh38.p7	14:70784485	CAGTGGCTCATGCCT[A/G]TAATCCCACAACTTT	4293
rs8007131	snp	A/C	0.222928	0.24853	intron-variant, upstream-variant-2KB	MAP3K9	GRCh38.p7	14:70754806	TTAAAATGATTAAGA[A/C]AATGCCTCCACCTCA	4293
rs8008147	snp	C/T	0.021333	0.101051	intron-variant	MAP3K9	GRCh38.p7	14:70771050	gatataaagggattg[C/T]tttttttttttgctt	4293
rs8008415	snp	G/T	0.039522	0.134904	intron-variant	MAP3K9	GRCh38.p7	14:70731953	TCCCCAGGTGTCAGA[G/T]GTCGAGGGCAGTCAT	4293
rs8008802	snp	A/G	0.405776	0.195535	intron-variant	MAP3K9	GRCh38.p7	14:70741161	AAGGGCGCAATCTCC[A/G]CTTACTGCAACCTCC	4293
rs8010714	snp	C/G	0.492871	0.0592773	intron-variant	MAP3K9	GRCh38.p7	14:70737448	ATTACTACACTATGA[C/G]TGCCTTGCCTGTGAA	4293
rs8011047	snp	A/G	0.34437	0.231505	intron-variant	MAP3K9	GRCh38.p7	14:70737652	CAACTGTACTACCAG[A/G]GCTGGGTTATTCTGC	4293

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