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
rs868227	snp	A/G	0.216649	0.247765	intron-variant	NSMCE2	GRCh38.p7	8:125251228	CCATACCCATTAGAA[A/G]GTTTCAGGGAGACGC	286053
rs954889	snp	A/G	0.163564	0.234582	intron-variant	NSMCE2	GRCh38.p7	8:125131544	CTGGGCAAGGTGTGC[A/G]TAAGTTCCAATATCT	286053
rs955840	snp	C/T	0	0	intron-variant	NSMCE2	GRCh38.p7	8:125209953	TTTATTTGCATAGGA[C/T]TTTGCAGTTTACAAA	286053
rs1106264	snp	A/G	0.0498117	0.149749	intron-variant	NSMCE2	GRCh38.p7	8:125181503	CTTCAACCTTTCTGC[A/G]TATTTGAAAATTTAT	286053
rs1109964	snp	A/G	0.0142736	0.0832652	intron-variant	NSMCE2	GRCh38.p7	8:125251607	CTTCTGCCCAGGAAT[A/G]TATGCTGGAAACTTG	286053
rs2293890	snp	C/G	0.478932	0.10045	intron-variant	NSMCE2	GRCh38.p7	8:125357656	ATCAACTTCCAGTAG[C/G]TGTTTCGTCCTAGTC	286053
rs2384859	snp	A/T	0.494526	0.0520291	intron-variant	NSMCE2	GRCh38.p7	8:125189884	CACAGAATATGGCTT[A/T]AGTCACTTAAGTGTG	286053
rs2384860	snp	G/T			intron-variant, downstream-variant-500B	NSMCE2	GRCh38.p7	8:125196013	tgcctcccaagtagc[G/T]gggattacagggccc	286053
rs2384862	snp	C/T			intron-variant, downstream-variant-500B	NSMCE2	GRCh38.p7	8:125196029	gggattacagggccc[C/T]gccaccatgtgaaag	286053
rs2384864	snp	A/C	0	0	intron-variant	NSMCE2	GRCh38.p7	8:125210338	CTGATATATGCTAAT[A/C]ATGTTTTTCTCTGGG	286053
rs2384865	snp	G/T	0	0	intron-variant	NSMCE2	GRCh38.p7	8:125210352	TAATGTTTTTCTCTG[G/T]GGAATTCTTCCTTTA	286053
rs2384866	snp	A/G			intron-variant	NSMCE2	GRCh38.p7	8:125210399	TTTTCCTGAAAGAGA[A/G]AGGCTCATTTGAGGG	286053
rs2384868	snp	C/T			intron-variant	NSMCE2	GRCh38.p7	8:125210444	CAATTTTTAATGTCC[C/T]CAGCAGCTTATAATA	286053
rs2384869	snp	A/G	0	0	intron-variant	NSMCE2	GRCh38.p7	8:125210456	TCCCCAGCAGCTTAT[A/G]ATAGACATTCAATAA	286053
rs2384870	snp	A/G			intron-variant	NSMCE2	GRCh38.p7	8:125217405	ttgctgtgtcaccca[A/G]gctgaagtgcagtgg	286053
rs2384871	snp	A/T			intron-variant	NSMCE2	GRCh38.p7	8:125217461	tgcctcccaggttca[A/T]gccattctcctgtct	286053
rs2384872	snp	C/T			intron-variant	NSMCE2	GRCh38.p7	8:125217509	ggactacggggcacc[C/T]accagccacacatgg	286053
rs2384873	snp	A/T	0	0	intron-variant	NSMCE2	GRCh38.p7	8:125217528	gccacacatggctaa[A/T]tttggttttttggaa	286053
rs2384874	snp	A/T	0	0	intron-variant	NSMCE2	GRCh38.p7	8:125218040	TAATTTGTTTATTCG[A/T]GTTGGTACATATTCT	286053
rs2384875	snp	G/T			intron-variant	NSMCE2	GRCh38.p7	8:125218044	TTGTTTATTCGAGTT[G/T]GTACATATTCTGCAT	286053
rs2384876	snp	G/T	0	0	intron-variant	NSMCE2	GRCh38.p7	8:125218068	TCTGCATAATATCAG[G/T]ATGTGCATTATTAGT	286053
rs2384877	snp	G/T	0.0850919	0.187897	intron-variant	NSMCE2	GRCh38.p7	8:125164895	ATTCAGTTATCTCCG[G/T]TTGAATAATTGTTTT	286053
rs2384878	snp	A/G			intron-variant	NSMCE2	GRCh38.p7	8:125243876	CATCTTTTCTTTCAA[A/G]GAGCAACAGGGAAGA	286053
rs2384879	snp	A/C			intron-variant	NSMCE2	GRCh38.p7	8:125243913	GTCACTGAAAAGACT[A/C]ACAACATATCCCACT	286053
rs2384882	snp	G/T	0.135825	0.222405	intron-variant	NSMCE2	GRCh38.p7	8:125178202	CTGACCCAACAGGCA[G/T]CGAGAAAGACACTAC	286053
rs2384883	snp	A/G	0	0	intron-variant	NSMCE2	GRCh38.p7	8:125114479	GGGTATAGGCATGGA[A/G]TGCATATATAATCCA	286053
rs2384884	snp	G/T			intron-variant	NSMCE2	GRCh38.p7	8:125114362	CTTTCatttattgag[G/T]gcttactgtgaatca	286053
rs2384885	snp	A/T			intron-variant	NSMCE2	GRCh38.p7	8:125114351	tgagggcttactgtg[A/T]atcatgtacctatag	286053
rs2384886	snp	C/G			intron-variant	NSMCE2	GRCh38.p7	8:125114335	atcatgtacctatag[C/G]caataccagcgggta	286053
rs2384887	snp	C/G			intron-variant	NSMCE2	GRCh38.p7	8:125114329	tacctatagccaata[C/G]cagcgggtaagggta	286053
rs2384888	snp	A/G	0.00597247	0.0543191	intron-variant	NSMCE2	GRCh38.p7	8:125114191	aagtattaaacagtc[A/G]agagaaaaataaagc	286053
rs2384889	snp	G/T			intron-variant	NSMCE2	GRCh38.p7	8:125111820	ATTATCAAGTAATTT[G/T]CAAACCAtttttttt	286053
rs2384890	snp	C/T	0.0482946	0.147699	intron-variant	NSMCE2	GRCh38.p7	8:125111179	CTGAAGTAACTGCCA[C/T]ACAGTGAAAACTTTT	286053
rs2384891	snp	G/T			intron-variant	NSMCE2	GRCh38.p7	8:125096462	TTCAGTGTAACCCAT[G/T]ATCTCATATATGATG	286053
rs2384892	snp	A/T			intron-variant	NSMCE2	GRCh38.p7	8:125096536	TTGAGTTTCTAGTGT[A/T]ATTTGTTTTTTTTTT	286053
rs2384893	snp	C/T			intron-variant	NSMCE2	GRCh38.p7	8:125101460	GATGTTTAGCAAGTC[C/T]TCCATGTTATGGTCC	286053
rs2384894	snp	C/T			intron-variant	NSMCE2	GRCh38.p7	8:125101473	CTCCATGTTATGGTC[C/T]ACCTGAATCCCATGA	286053
rs2384895	snp	C/T			intron-variant	NSMCE2	GRCh38.p7	8:125101475	CCATGTTATGGTCCA[C/T]CTGAATCCCATGAAA	286053
rs2384898	snp	G/T			intron-variant	NSMCE2	GRCh38.p7	8:125103450	ATTTGTGATGTGCCG[G/T]Ggtgtgatttttttt	286053
rs2384899	snp	A/G			intron-variant, upstream-variant-2KB	NSMCE2	GRCh38.p7	8:125129402	ggaaattgaggccca[A/G]agagataaagtcact	286053
rs2384900	snp	A/G			intron-variant, upstream-variant-2KB	NSMCE2	GRCh38.p7	8:125129409	gaggcccaaagagat[A/G]aagtcacttgtctaa	286053
rs2384901	snp	C/T			intron-variant, upstream-variant-2KB	NSMCE2	GRCh38.p7	8:125129463	gtgcTTCTTCATTCC[C/T]ACTTAGTTTATTTGC	286053
rs2384902	snp	A/G			intron-variant, upstream-variant-2KB	NSMCE2	GRCh38.p7	8:125129530	TGAAGATAGTGTTAG[A/G]AAAAGATTTGGCTCt	286053
rs2384904	snp	G/T			intron-variant	NSMCE2	GRCh38.p7	8:125147368	TATTGAAGGAAGAGC[G/T]TGATATAATTCTTTG	286053
rs2384905	snp	A/C			intron-variant	NSMCE2	GRCh38.p7	8:125147371	TGAAGGAAGAGCGTG[A/C]TATAATTCTTTGGTG	286053
rs2384906	snp	G/T			intron-variant	NSMCE2	GRCh38.p7	8:125147384	TGATATAATTCTTTG[G/T]TGGATCCTAAGAACA	286053
rs2384907	snp	A/C			intron-variant	NSMCE2	GRCh38.p7	8:125147455	TTGGTGAAAGGAAAC[A/C]AATGCAGATTAGAAA	286053
rs2384908	snp	A/G			intron-variant	NSMCE2	GRCh38.p7	8:125147494	TGGTGGTGGTCCCAA[A/G]ATATCAAAAGTGTAT	286053
rs2384909	snp	G/T	0	0	intron-variant	NSMCE2	GRCh38.p7	8:125251459	CTAAGTTTCCTCTTC[G/T]ACATTAATATGTTAA	286053
rs2384912	snp	C/T			intron-variant	NSMCE2	GRCh38.p7	8:125251401	TCACTGTCTCACCAT[C/T]AAGACCCGAGATATA	286053
rs2384913	snp	A/T	0	0	intron-variant	NSMCE2	GRCh38.p7	8:125251392	CACCATCAAGACCCG[A/T]GATATAATTTTCCAT	286053
rs2384914	snp	A/T	0.4941	0.0539917	intron-variant	NSMCE2	GRCh38.p7	8:125133125	TATTAATTAGATTTT[A/T]AAAATCCATTTTAAA	286053
rs2385092	snp	A/G	0.387832	0.208572	intron-variant	NSMCE2	GRCh38.p7	8:125334735	GCAGACTATGTGTAC[A/G]AAGGATTGGGCCAAA	286053
rs2385093	snp	A/G			intron-variant	NSMCE2	GRCh38.p7	8:125334803	tttttttttttttga[A/G]acacagtctcgctct	286053
rs2385094	snp	C/T	0.295343	0.245854	intron-variant	NSMCE2	GRCh38.p7	8:125344207	TTTCAATTTGACTAA[C/T]TGAATAAACAAATCC	286053
rs2385095	snp	A/G			intron-variant	NSMCE2	GRCh38.p7	8:125356870	CAAGGCTGTAAAGCA[A/G]AGGCTTTAAAAAAGG	286053
rs2891623	snp	A/T			intron-variant	NSMCE2	GRCh38.p7	8:125186823	TTTACCATCCCCAGA[A/T]TACAAACCTAACAGA	286053
rs2891626	snp	A/C	0	0	intron-variant	NSMCE2	GRCh38.p7	8:125210588	AGTCTCTTTCTCTTT[A/C]TGGTCCATCTTACCC	286053
rs2891627	snp	A/G			intron-variant	NSMCE2	GRCh38.p7	8:125162197	TTTTGAAAAGCTGCA[A/G]CAATACTTCTCAGGA	286053
rs2891628	snp	A/C/T	0.000399281	0.0141238	intron-variant	NSMCE2	GRCh38.p7	8:125243930	AACATATCCCACTTT[A/C/T]TGTATAAATCCCCCA	286053
rs2891629	snp	A/C			intron-variant	NSMCE2	GRCh38.p7	8:125180634	TAATGCTAAGACTCC[A/C]AGTTAGATACAGAAA	286053
rs2891630	snp	C/T	0.4944	0.0526182	intron-variant	NSMCE2	GRCh38.p7	8:125177849	TTTAAAATGAGGGCA[C/T]TGGAAGAAAAAGAAG	286053
rs2891631	snp	A/T			intron-variant	NSMCE2	GRCh38.p7	8:125147465	GAAACCAATGCAGAT[A/T]AGAAAGGAAAGATTG	286053
rs2891632	snp	A/G	0.000399281	0.0141238	intron-variant	NSMCE2	GRCh38.p7	8:125147502	GTCCCAAAATATCAA[A/G]AGTGTATGTGTTAAG	286053
rs2891633	snp	A/G	0.0256215	0.110247	intron-variant	NSMCE2	GRCh38.p7	8:125131077	acttccttcagtgac[A/G]tttgtcatgcatttg	286053
rs2891634	snp	G/T	0	0	intron-variant	NSMCE2	GRCh38.p7	8:125132437	AGTGTGATAGCAGTG[G/T]TCTTGAATCCTAAGG	286053
rs2891635	snp	C/T			intron-variant, upstream-variant-2KB, utr-variant-5-prime	KIAA0196, NSMCE2	GRCh38.p7	8:125091156	ATACTGATGTCAAAA[C/T]CCTTTGCATTTGGGG	286053
rs2891677	snp	C/T	0.475259	0.108435	intron-variant	NSMCE2	GRCh38.p7	8:125331966	TTTCTCTAAGGAGAT[C/T]AAAGCTGCTTTGTGG	286053
rs2891678	snp	A/C	0.46703	0.124089	intron-variant	NSMCE2	GRCh38.p7	8:125349383	AATAAGCATTTCAAG[A/C]AGGCAACAAATATTT	286053
rs2954164	snp	A/G	0.00318978	0.0398085	intron-variant	NSMCE2	GRCh38.p7	8:125288863	aggctgcagtgagcc[A/G]agatcgagccactgc	286053
rs3763593	snp	A/G	0.137867	0.223442	intron-variant	NSMCE2	GRCh38.p7	8:125093921	TTGTCCTAGACCCTC[A/G]GAAGGCTGAGGTGGG	286053
rs3812467	snp	C/T	0.19334	0.243495	intron-variant	NSMCE2	GRCh38.p7	8:125290547	AAAGAGGATACATAA[C/T]CTAGAATGCTATGAG	286053
rs3923300	snp	C/G	0.206967	0.246268	intron-variant, missense	NSMCE2	GRCh38.p7	8:125130234	GGGAAGAAGAGCACA[C/G]AGGTCAAGGGCCCTT	286053
rs3955403	snp	A/T	0.0882987	0.190664	intron-variant	NSMCE2	GRCh38.p7	8:125217359	tttatttatttattt[A/T]ttttttatttattta	286053
rs3955404	snp	C/T	0.430285	0.173197	intron-variant	NSMCE2	GRCh38.p7	8:125242017	TGTGAGAACTGCTTC[C/T]TTAATGCCCCTTTTG	286053
rs4006771	snp	C/T	0.0142736	0.0832652	intron-variant	NSMCE2	GRCh38.p7	8:125252006	TCAGACTCCAGACCA[C/T]ATTTCAATGGTTTAT	286053
rs4006772	snp	A/G	0.451359	0.148171	intron-variant	NSMCE2	GRCh38.p7	8:125251681	GAAAATAACTATTCC[A/G]TTGTCTAAGACATAA	286053
rs4006773	snp	G/T	0	0	intron-variant	NSMCE2	GRCh38.p7	8:125251433	TTAATCATATTCAAG[G/T]CTCTCCCATTTAAAA	286053
rs4006774	snp	G/T	0	0	intron-variant	NSMCE2	GRCh38.p7	8:125251310	TTTCCAGTTCATTTG[G/T]GGGCATTTTCTGTAT	286053
rs4006775	snp	G/T	0	0	intron-variant	NSMCE2	GRCh38.p7	8:125251065	TCAGATCATTTGCAG[G/T]CCTACCATCAAAGAC	286053
rs4006776	snp	A/G	0	0	intron-variant	NSMCE2	GRCh38.p7	8:125234369	ctgaaaaatacagat[A/G]actgtcttaactcac	286053
rs4006777	snp	C/G			intron-variant	NSMCE2	GRCh38.p7	8:125241094	ttgaatatccctaat[C/G]tgaaaatctgaagtc	286053
rs4006778	snp	A/C	0	0	intron-variant	NSMCE2	GRCh38.p7	8:125244078	GACTAGCAGTTGTTA[A/C]CAGAGTGGTGTGCCA	286053
rs4242367	snp	A/G	0.499396	0.0173617	intron-variant	NSMCE2	GRCh38.p7	8:125290027	TCATTTCCATTCAAG[A/G]GCAGAACATCAAAGA	286053
rs4242368	snp	C/T	0.397271	0.202018	intron-variant	NSMCE2	GRCh38.p7	8:125356998	ACTTTAAAAAAGATT[C/T]TTTTTAACTGCTCTG	286053
rs4278169	snp	C/T	0.0498117	0.149749	intron-variant	NSMCE2	GRCh38.p7	8:125217988	AAGCAGAAGTCTCTA[C/T]GCTATTTTAATTGTT	286053
rs4279612	snp	C/T	0.234692	0.249531	intron-variant	NSMCE2	GRCh38.p7	8:125285145	CTAAAACTAAAATGG[C/T]ACAGTTTGCTTTGGA	286053
rs4294203	snp	A/G	0.234109	0.249494	intron-variant	NSMCE2	GRCh38.p7	8:125281763	tttttttttttttaa[A/G]gagatggggtcttgc	286053
rs4300023	snp	C/T	0.494609	0.0516363	intron-variant	NSMCE2	GRCh38.p7	8:125132007	TCATGTCATGCATCC[C/T]TAGAGTTTCTCAGGT	286053
rs4319117	snp	C/T	0.289165	0.246913	intron-variant	NSMCE2	GRCh38.p7	8:125349522	GCCTCAAGGGATCCT[C/T]CCACCTTGGCCTTCC	286053
rs4330708	snp	G/T	0.4941	0.0539917	intron-variant	NSMCE2	GRCh38.p7	8:125220957	AACTTGGGCCCTGTG[G/T]GTGCTAAAAATATCT	286053
rs4338125	snp	A/G	0.0142736	0.0832652	intron-variant	NSMCE2	GRCh38.p7	8:125240359	tgaactcctgacctc[A/G]tgatcagcccgcctt	286053
rs4339663	snp	C/T	0.287606	0.247155	intron-variant	NSMCE2	GRCh38.p7	8:125272792	GTATATATATACACA[C/T]GTGTATATATATACA	286053
rs4350000	snp	A/G	0.245916	0.249967	intron-variant	NSMCE2	GRCh38.p7	8:125261583	CTGGAAATTTAATTA[A/G]TATACTTACACTTTG	286053
rs4360308	snp	A/G	0.134119	0.221521	intron-variant	NSMCE2	GRCh38.p7	8:125190746	ATAATACAGGTCATA[A/G]GCATGCTTTGTATAA	286053
rs4367569	snp	G/T	0.446249	0.154875	intron-variant	NSMCE2	GRCh38.p7	8:125272864	ACACACACATATATA[G/T]ACACACGTATACGTG	286053
rs4372018	snp	C/T	0.469445	0.119766	intron-variant	NSMCE2	GRCh38.p7	8:125252474	gagctcgcagtgagc[C/T]gagatcccgccactg	286053
rs4464986	snp	A/G	0.279726	0.248226	intron-variant	NSMCE2	GRCh38.p7	8:125285578	TTACTTTAAACATGT[A/G]CATTTAGGTAACACT	286053
rs4466418	snp	C/T	0.480302	0.0972668	intron-variant	NSMCE2	GRCh38.p7	8:125311545	ATATTGCACAACATA[C/T]CACGAATAAAGCATG	286053
rs4477044	snp	A/T	0.174288	0.23826	intron-variant	NSMCE2	GRCh38.p7	8:125217328	AACTGATCACTTTTT[A/T]AAAAAATTTTATTTA	286053

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