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
rs1374529	snp	C/G	0	0	intron-variant	INTS12	GRCh38.p7	4:105697412	TCTCTTCCCCCCTCA[C/G]AGGTAACCACTATTC	57117
rs3213950	snp	C/T	0.00546505	0.0519871	utr-variant-5-prime, nc-transcript-variant	INTS12	GRCh38.p7	4:105700012	AGCAGCCATTGCAAA[C/T]GCCTGAAGGAAAAAA	57117
rs3756260	snp	C/G	0.46974	0.119223	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	GSTCD, INTS12	GRCh38.p7	4:105708873	CGTTTTTCTCCTGGC[C/G]TCTGTGGAGGCGAGT	57117
rs3796924	snp	C/G	0.000399281	0.0141238	intron-variant	INTS12	GRCh38.p7	4:105688603	ATCTTATCCTTCATT[C/G]CAAAACCATGTTACG	57117
rs3796925	snp	A/G	0.00796804	0.0626141	intron-variant	INTS12	GRCh38.p7	4:105701651	CTTTTTTTTCTTTAA[A/G]TTCCACTCCTGTGAC	57117
rs4434257	snp	A/T	0.100231	0.200173	intron-variant	INTS12	GRCh38.p7	4:105698220	CCTTCCTCATTAATG[A/T]AAATGAATATCAACC	57117
rs4490460	snp	C/T	0.245631	0.249962	intron-variant	INTS12	GRCh38.p7	4:105697912	aaaattagccaagca[C/T]ggtggcatgcacctg	57117
rs4699196	snp	C/T	0.463666	0.129795	upstream-variant-2KB, intron-variant	GSTCD, INTS12	GRCh38.p7	4:105709792	TGTATTTCTATTTTA[C/T]CTAAGCTTATCTGTA	57117
rs5860807	in-del	-/T	0.307176	0.243374	intron-variant	INTS12	GRCh38.p7	4:105698554	AAAACAATTTTTTTT[-/T]CTTTAGTAATAATAG	57117
rs6820671	snp	A/G	0.345925	0.230864	intron-variant	INTS12	GRCh38.p7	4:105692664	TATATAGAATGCCTT[A/G]ATTAAATTTGGCTAT	57117
rs6850604	snp	G/T	0.0566069	0.158427	intron-variant, upstream-variant-2KB	INTS12, GSTCD	GRCh38.p7	4:105707223	ACTGACAGCTGCTGT[G/T]CCCCTCTCCATTCCA	57117
rs7659526	snp	C/T	0.347694	0.230122	intron-variant	INTS12	GRCh38.p7	4:105700486	AATGGTGAAAAGGTA[C/T]ATTAAGTGATTAGCT	57117
rs10008158	snp	A/G	0	0	synonymous-codon, nc-transcript-variant	INTS12	GRCh38.p7	4:105683066	AGTGGGCGTAGTGCT[A/G]TTATTGGAACCTATT	57117
rs10016392	snp	C/T	0.000399281	0.0141238	intron-variant	INTS12	GRCh38.p7	4:105701606	AAACCTGCCATTCCC[C/T]CAGCATATACAAGGG	57117
rs10516523	snp	G/T	0.46974	0.119223	intron-variant	INTS12	GRCh38.p7	4:105704106	CTTTTATAGCAAAAC[G/T]TTCTCAGAAATCATA	57117
rs10615792	in-del	-/AT	0.223225	0.248562	intron-variant	INTS12	GRCh38.p7	4:105690459	ATAGATTTCAGAGAC[-/AT]ATAAGAGGTAGAATT	57117
rs10672030	in-del	-/T	0	0	upstream-variant-2KB, intron-variant	GSTCD, INTS12	GRCh38.p7	4:105710233	TTTTTTTTTTTTTTT[-/T]GAGCTGGAGTCCTGC	57117
rs11726569	snp	A/G	0.0614824	0.164198	intron-variant	INTS12	GRCh38.p7	4:105685451	CTATATGACAAATCA[A/G]TAATGGATATGCCTT	57117
rs11727189	snp	G/T	0.0614824	0.164198	intron-variant	INTS12	GRCh38.p7	4:105697983	tgaacctgggaggga[G/T]agagcgcagtgagcc	57117
rs11727735	snp	A/G	0.0486741	0.148216	upstream-variant-2KB, intron-variant	GSTCD, INTS12	GRCh38.p7	4:105710713	TGTGAAAATTCAGTA[A/G]TTTTATTTCATACTT	57117
rs11728044	snp	C/G	0.0622301	0.165053	intron-variant	INTS12	GRCh38.p7	4:105683629	TAGTGCTTTAACATA[C/G]TTTTTACCCAACAAA	57117
rs11940951	snp	A/G	0	0	intron-variant, upstream-variant-2KB	INTS12, GSTCD	GRCh38.p7	4:105707034	AAATTTCTTGGCCTA[A/G]CATTTAAGAAGATTC	57117
rs11941690	snp	A/C	0.471768	0.115407	intron-variant	INTS12	GRCh38.p7	4:105690103	AGCTGAGAAGCAGAA[A/C]ATATGGGAACATGAA	57117
rs12374256	snp	A/G	0.0629771	0.165899	intron-variant	INTS12	GRCh38.p7	4:105696204	ttgacatatgtatac[A/G]tctgtgacaccatca	57117
rs12507921	snp	A/G	0	0	intron-variant	INTS12	GRCh38.p7	4:105695025	tgcctcctgggctca[A/G]gcaatcctcccaccc	57117
rs13111824	snp	G/T			upstream-variant-2KB, intron-variant	GSTCD, INTS12	GRCh38.p7	4:105710493	ctcggcttcccaaag[G/T]ggtgggattacaggc	57117
rs13132641	snp	A/T	0.0131051	0.0798799	intron-variant	INTS12	GRCh38.p7	4:105684775	GTTATGAAAGACCTA[A/T]TTTTTTTTCCTTTTC	57117
rs13142949	snp	C/T			intron-variant	INTS12	GRCh38.p7	4:105702131	atttatttctatttc[C/T]ttttttttttttttt	57117
rs17036109	snp	A/G	0.00953873	0.0683987	intron-variant	INTS12	GRCh38.p7	4:105684085	ACAGTGACATTTTGG[A/G]TAGGACTGATCTCAT	57117
rs17036120	snp	C/G	0.0614824	0.164198	intron-variant	INTS12	GRCh38.p7	4:105700351	CAGTACATAGAACTT[C/G]ATGGGTTTACGTCAA	57117
rs17036123	snp	C/T	0.0622301	0.165053	intron-variant	INTS12	GRCh38.p7	4:105701033	TGCAGCACACTTGCA[C/T]TGCTATAGTTAGGGA	57117
rs17036125	snp	A/T	0.0614824	0.164198	intron-variant	INTS12	GRCh38.p7	4:105702517	TATAATTGATCTTTA[A/T]CCTCAAGGAGCTTTA	57117
rs17036129	snp	C/T	0.0486741	0.148216	intron-variant	INTS12	GRCh38.p7	4:105703372	AATTCTTAGGTGATG[C/T]TGGGAATTAGCTGTG	57117
rs17036133	snp	A/C	0.0248432	0.108648	intron-variant	INTS12	GRCh38.p7	4:105703576	TCCCTACTTTATAGA[A/C]ATCCACCCTGCTAGC	57117
rs17262443	snp	C/T	0.110167	0.207236	intron-variant	INTS12	GRCh38.p7	4:105693649	AGATCTGTAGAAGAA[C/T]TGCAATGAATTTATT	57117
rs17262457	snp	C/T	0.109461	0.206758	intron-variant	INTS12	GRCh38.p7	4:105697205	ATAGCTTTGCTGATA[C/T]AGATAACTTGTTATT	57117
rs17262764	snp	A/G	0.46974	0.119223	intron-variant, upstream-variant-2KB	INTS12, GSTCD	GRCh38.p7	4:105707852	TCTGTGATCTCTCCA[A/G]TCTAAATTGGGCATT	57117
rs28391170	snp	A/C	0.342134	0.232404	intron-variant, upstream-variant-2KB, utr-variant-5-prime	INTS12, GSTCD	GRCh38.p7	4:105708089	CTTCCAATAAACATT[A/C]TTTTAAAGATGCTGC	57117
rs28403197	snp	A/G	0.171704	0.237423	intron-variant, upstream-variant-2KB, utr-variant-5-prime	INTS12, GSTCD	GRCh38.p7	4:105708410	TGTCCCTAGACCTAG[A/G]AATATGCTCGGTCCG	57117
rs28414565	snp	A/C	0.172351	0.237636	intron-variant	INTS12	GRCh38.p7	4:105683672	TTAGTTAAACATCTA[A/C]TTCTTTTAGACTTTT	57117
rs28450989	snp	C/G	0.328148	0.237472	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	GSTCD, INTS12	GRCh38.p7	4:105708850	TATTTTCCACATAAG[C/G]TGGCTGTCGTTTTTC	57117
rs28628106	snp	C/T	0.46974	0.119223	intron-variant	INTS12	GRCh38.p7	4:105686084	TTTCTTTTTTTGAGT[C/T]GCAGTTTCGCTCTTG	57117
rs28642176	snp	A/C	0.171704	0.237423	intron-variant	INTS12	GRCh38.p7	4:105705027	ATCACTTCTCACAAT[A/C]CAAAGGTTCAAGAAT	57117
rs34072732	snp	A/G	0.0978298	0.198354	synonymous-codon, nc-transcript-variant	INTS12	GRCh38.p7	4:105683207	CAATTTTGCTGTTGA[A/G]GGACCAGCAGAGGAA	57117
rs34166034	in-del	-/C			intron-variant, utr-variant-5-prime	INTS12	GRCh38.p7	4:105702893	TATCTTACCTTTACT[-/C]CCCCTTTTCTGTTGC	57117
rs34234581	snp	C/T	0.00192581	0.0309709	synonymous-codon, nc-transcript-variant, downstream-variant-500B	INTS12, ARHGEF38	GRCh38.p7	4:105682778	CTTCTTGACCATCTG[C/T]AATCGCTTCATAGCA	57117
rs34535300	in-del	-/C			intron-variant	INTS12	GRCh38.p7	4:105686102	GTTTCGCTCTTGTCA[-/C]CCCAGGCTGGAGTGC	57117
rs34567094	snp	C/T	0.0499671	0.149956	missense, nc-transcript-variant	INTS12	GRCh38.p7	4:105683155	GGTTAGCTGACGAAG[C/T]AGCAGGTTTCCCAGT	57117
rs34938249	in-del	-/G			intron-variant	INTS12	GRCh38.p7	4:105685801	AGGCCAAGATATTAA[-/G]GAAATAATGTAGTAT	57117
rs34969827	in-del	-/G			frameshift-variant, nc-transcript-variant, downstream-variant-500B	INTS12, ARHGEF38	GRCh38.p7	4:105682952	GGAACTAAACTACTT[-/G]GGACTAGGAAGACCT	57117
rs34994709	in-del	-/T			intron-variant, upstream-variant-2KB	INTS12, GSTCD	GRCh38.p7	4:105707316	TTCTCCCTTGAAGCA[-/T]TTTTTTTTTTTTTTT	57117
rs35236206	in-del	-/C			intron-variant	INTS12	GRCh38.p7	4:105697699	AAAGTCTGTTGATCA[-/C]CTGGTGTAGACTTAG	57117
rs35370743	snp	A/G	0.0904758	0.192489	synonymous-codon, nc-transcript-variant, downstream-variant-500B	INTS12, ARHGEF38	GRCh38.p7	4:105683033	CAAGGTTAGAGGTGG[A/G]GGTGGTTTTAAAGGT	57117
rs35485586	in-del	-/T			intron-variant	INTS12	GRCh38.p7	4:105698885	TGTTCTATTTTCTCC[-/T]TTCTCAGTTTGGGAT	57117
rs35650037	snp	G/T			upstream-variant-2KB, intron-variant	GSTCD, INTS12	GRCh38.p7	4:105710496	GGCTTCCCAAAGGGG[G/T]GGGATTACAGGCGTG	57117
rs35695511	snp	A/C/G	0.00382332	0.0435557	synonymous-codon, nc-transcript-variant	INTS12	GRCh38.p7	4:105692054	CTTGTCTGTCACCTG[A/C/G]GGTTTATGACAATCT	57117
rs35859278	in-del	-/T			intron-variant	INTS12	GRCh38.p7	4:105698892	TTTTCTCCTTCTCAG[-/T]TTTGGGATCTAAGTC	57117
rs36020924	in-del	-/T			intron-variant	INTS12	GRCh38.p7	4:105698840	GATCCTCTCTTGAGC[-/T]TTCAGATTCTGGTTA	57117
rs36071022	in-del	-/C			intron-variant	INTS12	GRCh38.p7	4:105684783	GACCTAATTTTTTTT[-/C]CCTTTTCTTGCTATT	57117
rs56843185	snp	A/G	0.108755	0.206276	upstream-variant-2KB, intron-variant	GSTCD, INTS12	GRCh38.p7	4:105710152	ATTTCTTTTTATTTT[A/G]TATACTTTGCACTTC	57117
rs57389075	in-del	-/TT			intron-variant	INTS12	GRCh38.p7	4:105701250	TTTTTTTTTTTTTTT[-/TT]AAGTTCCCAGGAAGG	57117
rs57790298	in-del	-/TT			intron-variant, upstream-variant-2KB	INTS12, GSTCD	GRCh38.p7	4:105707331	TTTTTTTTTTTTTTT[-/TT]GGCACAAGTGTTATG	57117
rs57956021	snp	A/G			intron-variant	INTS12	GRCh38.p7	4:105689362	CCAATGCACATATGA[A/G]AATCTCACTCAAAGC	57117
rs59677702	snp	G/T	0.000798403	0.0199641	intron-variant	INTS12	GRCh38.p7	4:105685694	TTCTTCCATATTTAG[G/T]GCTATGCTTAATATT	57117
rs61732560	snp	A/G	0.00072678	0.0190489	synonymous-codon, nc-transcript-variant	INTS12	GRCh38.p7	4:105693313	CCTACAAACAACGCA[A/G]GCCAATCCCATCTCC	57117
rs62320293	snp	C/T	0.5	0	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	INTS12, ARHGEF38	GRCh38.p7	4:105682729	AAAAACCTACTTGGC[C/T]ACATTACTTCTTGAG	57117
rs62320294	snp	C/G/T	1.6476e-05	0.00287014	missense, nc-transcript-variant	INTS12	GRCh38.p7	4:105683158	TAGCTGACGAAGTAG[C/G/T]AGGTTTCCCAGTATT	57117
rs62320295	snp	A/G/T	6.87924e-05	0.00586442	missense, synonymous-codon, nc-transcript-variant	INTS12	GRCh38.p7	4:105683279	TACTGACGAGGAAAC[A/G/T]CTGGCACTAGAAGAA	57117
rs62320296	snp	C/T	0.0372196	0.131242	intron-variant	INTS12	GRCh38.p7	4:105696093	CGGCCTCAAATGATC[C/T]GCCCACCTCGGCCTC	57117
rs62320297	snp	C/T	0.202035	0.245356	intron-variant, upstream-variant-2KB	INTS12, GSTCD	GRCh38.p7	4:105706791	TCCTGTGGATTCTGA[C/T]GGCAATATTTTTCAC	57117
rs70941208	in-del	-/A	0	0	intron-variant, upstream-variant-2KB	INTS12, GSTCD	GRCh38.p7	4:105706971	AAATAAAAAAAAAAA[-/A]TTCTTGCTGAGAAGT	57117
rs70941210	in-del	-/T	0.375	0.216506	upstream-variant-2KB, intron-variant	GSTCD, INTS12	GRCh38.p7	4:105710399	TTTTTTTTTTTTTTT[-/T]CAGTCGAGGAGGGGT	57117
rs71586112	in-del	-/A	0.5	0	intron-variant, upstream-variant-2KB	INTS12, GSTCD	GRCh38.p7	4:105706960	CTTTTTCATTAAAAT[-/A]AAAAAAAAAAATTCT	57117
rs72671808	snp	A/C	0.0618563	0.164627	intron-variant	INTS12	GRCh38.p7	4:105684563	ATAGAGTTCTGAGAT[A/C]TTCGATTTATAAGAG	57117
rs72671809	snp	A/C	0.0622301	0.165053	intron-variant	INTS12	GRCh38.p7	4:105690380	GAGGCAAGGAGATTT[A/C]TTAAGTGGCTATTGC	57117
rs72671810	snp	C/T	0.0486741	0.148216	intron-variant	INTS12	GRCh38.p7	4:105692596	AACAAACCCCAACAC[C/T]TGGCATGCACAAAAG	57117
rs72671811	snp	C/T	0.0614824	0.164198	intron-variant	INTS12	GRCh38.p7	4:105694446	TTCTCACGTCTCAGC[C/T]TCCTGAGGTGCTGGA	57117
rs72671812	snp	A/G	0.0189856	0.0955633	intron-variant	INTS12	GRCh38.p7	4:105696133	TGGGATTAAAGACGT[A/G]TACCACCACACCTGG	57117
rs72671813	snp	A/G			intron-variant	INTS12	GRCh38.p7	4:105696608	TTTATCAATTTACCT[A/G]TTGATGGATATTTGG	57117
rs72671815	snp	A/G	0.0622301	0.165053	intron-variant	INTS12	GRCh38.p7	4:105697062	GTTTGTTTTATTACT[A/G]AGTTAAAAGAGTTCT	57117
rs72671820	snp	C/T	0.0934081	0.194882	intron-variant	INTS12	GRCh38.p7	4:105699826	TTACAAAACTCTCTC[C/T]AAGCTTTTTATTCAT	57117
rs72671824	snp	A/G	0.0622301	0.165053	intron-variant	INTS12	GRCh38.p7	4:105702066	TAACATGGCCCTTTG[A/G]CCCAGTGGTCCCCAT	57117
rs72671826	snp	C/T	0.0486741	0.148216	intron-variant	INTS12	GRCh38.p7	4:105703345	GTGGTAGTAGTAGTA[C/T]TGATAGGAGTGAATT	57117
rs72671828	snp	C/T	0.0618563	0.164627	intron-variant	INTS12	GRCh38.p7	4:105703643	ACTGGGAGGAATATA[C/T]ATACATTCTATCTTC	57117
rs72671835	snp	C/T	0.0614824	0.164198	upstream-variant-2KB, intron-variant	GSTCD, INTS12	GRCh38.p7	4:105710199	AATTTAAACACAGCT[C/T]AAACTTGAGCTTCTG	57117
rs72969245	snp	A/G	0.0134861	0.0810011	intron-variant	INTS12	GRCh38.p7	4:105683892	AAATTTTGAGCAACA[A/G]TTACAGGAGTACAAA	57117
rs72969249	snp	A/G	0.0640965	0.167152	intron-variant	INTS12	GRCh38.p7	4:105691839	TAATCACATGTACAT[A/G]CTATACATATAAATA	57117
rs72969253	snp	A/T	0.0566069	0.158427	intron-variant	INTS12	GRCh38.p7	4:105704917	CTAGCATCATCTATT[A/T]TCTGGCCCACTGCAA	57117
rs72969258	snp	C/T	0.0134861	0.0810011	upstream-variant-2KB, intron-variant	GSTCD, INTS12	GRCh38.p7	4:105710531	ACCGCGCCCGGCCTG[C/T]TTTTGTTTTTTTAAA	57117
rs73837096	snp	A/C	0.109461	0.206758	intron-variant	INTS12	GRCh38.p7	4:105685412	AACTGGTTATTCTTA[A/C]TTCTATTCCAATTCA	57117
rs73837101	snp	C/T	0.0138799	0.0821421	intron-variant	INTS12	GRCh38.p7	4:105700361	AACTTGATGGGTTTA[C/T]GTCAAGTTTACTCTG	57117
rs73837102	snp	C/T	0.5	0	intron-variant	INTS12	GRCh38.p7	4:105700820	TACATCAAAGGCTTA[C/T]GAAATTCCACAATAC	57117
rs73839003	snp	A/C	0.0494327	0.149241	intron-variant	INTS12	GRCh38.p7	4:105701473	ATTATTATATACATC[A/C]CCTCTACATAATGAT	57117
rs73839004	snp	A/G	0.109814	0.206997	intron-variant	INTS12	GRCh38.p7	4:105704479	AACTCTGGGAGTAGG[A/G]TCTAGAAATCTGTGT	57117
rs73839006	snp	C/T	0.108755	0.206276	intron-variant	INTS12	GRCh38.p7	4:105706681	TCCTGCTCTTACTTT[C/T]AATAAATGACACAAC	57117
rs74317794	snp	A/C			intron-variant	INTS12	GRCh38.p7	4:105683981	TCATGATTTTAGTTT[A/C]ACAATTTGCCCATGA	57117
rs74464047	snp	C/T	0.108755	0.206276	intron-variant	INTS12	GRCh38.p7	4:105698156	AGCAAAAAAGTTGTT[C/T]TAGTTGTTGACGGAT	57117
rs74497593	snp	C/T	0.0622301	0.165053	intron-variant	INTS12	GRCh38.p7	4:105695057	CCACCCGCCCACAAA[C/T]AGCTGGGACTACAGG	57117
rs74516377	snp	C/G/T			intron-variant	INTS12	GRCh38.p7	4:105691493	GAGGACAATGAGAAG[C/G/T]AAAGACTAAGCAACA	57117
rs74673939	snp	C/T	0.0193772	0.0965046	intron-variant	INTS12	GRCh38.p7	4:105689499	CTTTTGGTATTTCCC[C/T]ACATTTGCTCTTGGT	57117

Full records

It may take some time, please wait.