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
rs13723	snp	C/T	0.494774	0.0508504	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614868	CTCCTGGGCTCAGGG[C/T]CCATCAGGCAGCCTC	124930
rs191315	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29609947	catggcctctcaaag[C/T]gctgggattacaggc	124930
rs330159	snp	A/G	0.4928	0.0595664	intron-variant	ANKRD13B	GRCh38.p7	17:29609976	aaactcctgacctca[A/G]gtgatccgctcacct	124930
rs330160	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29609931	gctgggattacaggc[A/G]tgagccaccatgccc	124930
rs1064133	snp	A/G	0	0	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614729	TTTATTTGTGCCTCA[A/G]AATCAGTCTGGTGCC	124930
rs1443346	snp	C/T	0.161267	0.233723	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592507	CCTCCACCCAGCTGG[C/T]CCTTCAGGAAGGGAA	124930
rs1529421	snp	C/G	0	0	intron-variant	ANKRD13B	GRCh38.p7	17:29608580	ACTCTTTCatccatt[C/G]tttcaacaaatattt	124930
rs1971157	snp	C/G	0.442926	0.158996	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598325	GCATGACCATGAACT[C/G]CATTGTCAAAAATGA	124930
rs2016002	snp	A/C	0	0	intron-variant	ANKRD13B	GRCh38.p7	17:29606882	ggtgaaaacccatct[A/C]tactaaaaatacaaa	124930
rs2114877	snp	C/G	0.29046	0.246704	intron-variant	ANKRD13B	GRCh38.p7	17:29603900	tttttttttgagatg[C/G]agtctctctctctgt	124930
rs2321204	snp	C/T	0	0	intron-variant	ANKRD13B	GRCh38.p7	17:29602675	ttaagttaaggatct[C/T]aagatgaaataatcc	124930
rs3098944	snp	C/T	0.474723	0.109542	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598794	ggaggccaaagtagg[C/T]ggatcacttgagctc	124930
rs3098945	snp	A/G	0.368733	0.220005	intron-variant	ANKRD13B	GRCh38.p7	17:29597161	GTATGGACTAAACAC[A/G]GTGCTTGCGAGGAAG	124930
rs3098946	snp	G/T	0.123452	0.215605	intron-variant	ANKRD13B	GRCh38.p7	17:29594884	CAGCCTGCTCAGTCC[G/T]ATGGCCTGCCCTCCA	124930
rs3110492	snp	A/G	0.449599	0.150533	intron-variant	ANKRD13B	GRCh38.p7	17:29595257	GCAAGTGTGAACAGG[A/G]AATTCCAGGGTGATG	124930
rs7220401	snp	C/T	0.499908	0.00678851	intron-variant	ANKRD13B	GRCh38.p7	17:29608670	GTCCCGACCTCAGGT[C/T]GCTCTTCTGTGTGAG	124930
rs7226173	snp	G/T	0	0	intron-variant	ANKRD13B	GRCh38.p7	17:29595452	CCTGAGGGTGGGTGG[G/T]CCTTTTACTGCAGAG	124930
rs7406075	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29607562	CTGTCTTTCCGTTGC[C/T]CATAGTGTCTGTCTT	124930
rs8065982	snp	A/G	0.0360663	0.129354	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614801	GGGGGGAACGCCTAC[A/G]GTGTGGGTTGGGGTC	124930
rs9674809	snp	A/G	0.0535932	0.154675	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29599200	cctggagaacgttcc[A/G]gggaaggCCATTGGC	124930
rs9709449	snp	C/G/T	0	0	intron-variant	ANKRD13B	GRCh38.p7	17:29606612	TAACAAACATGCTTT[C/G/T]TAAgccaggtgcagg	124930
rs9894979	snp	C/G/T	0.0134861	0.0810011	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614787	ACCTAACTTTACTTG[C/G/T]GGGGAACGCCTACGG	124930
rs9901272	snp	C/T	0.0905309	0.192535	intron-variant	ANKRD13B	GRCh38.p7	17:29605435	acacacacacacaca[C/T]acacacacacatata	124930
rs9911167	snp	C/T	0.46865	0.121211	intron-variant	ANKRD13B	GRCh38.p7	17:29608528	TCTTTTTCACTGTTG[C/T]ATTCCCAGTGGCTGG	124930
rs11080107	snp	C/T	0.495818	0.0455352	intron-variant	ANKRD13B	GRCh38.p7	17:29611406	GGCCCTGGCCCCTGG[C/T]CCTTGAAGCACTCAG	124930
rs11436597	in-del	-/C	0.0955749	0.196603	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592886	CGACCTAGGCCCGTG[-/C]CCCCCCCACTTCCCC	124930
rs11447635	in-del	-/A	0.503626	0.064491	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29599386	TAGAGCCTGGCAACC[-/A]GGGGAGCAGCAAAGA	124930
rs11553124	snp	C/T	0	0	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614728	GGGCACCAGACTGAT[C/T]CTGAGGCACAAATAA	124930
rs11651605	snp	G/T	0	0	intron-variant	ANKRD13B	GRCh38.p7	17:29605040	CTCCTTTTTGTGtgg[G/T]cttactgagtttcac	124930
rs12452244	snp	C/T	0.00358779	0.0422022	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29593043	CTCTTCGGCCACCTG[C/T]CACCCCCAGTTTCAC	124930
rs12601861	snp	A/G	0.444444	0.157135	intron-variant	ANKRD13B	GRCh38.p7	17:29604393	tttgtattttttgta[A/G]acatggggttttggt	124930
rs12943142	snp	C/G			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598422	CACCTCCCCAGCACT[C/G]TGGACTCCTTTTGTC	124930
rs12943198	snp	A/C			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598475	AATATATTGTTTATA[A/C]TGccctctcccctcc	124930
rs12951819	snp	A/T			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598441	ACTCCTTTTGTCATT[A/T]ACCTCCCTAATTATA	124930
rs28699506	snp	A/G	0.0172401	0.0912295	intron-variant	ANKRD13B	GRCh38.p7	17:29600268	TTGGGTCATATTTAA[A/G]AATGGGGCTGGGGAG	124930
rs34249921	in-del	-/G			intron-variant	ANKRD13B	GRCh38.p7	17:29597309	CACACACGTTACACA[-/G]GGAGTGGACTCCTGC	124930
rs34261270	in-del	-/A			intron-variant	ANKRD13B	GRCh38.p7	17:29607063	CCCCAAAAAAAACAC[-/A]AAAAAAAAACCCCAA	124930
rs34361929	snp	C/G			missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612246	TTCATCACCCTGCGT[C/G]TGCCTCCTGGCTTCC	124930
rs34391066	in-del	-/G			intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612843	GGCGCGCGGGGCCAC[-/G]GGGACTCCGCGCCGC	124930
rs34435725	in-del	-/C			intron-variant	ANKRD13B	GRCh38.p7	17:29603398	CTGCTTGCCACCATG[-/C]CCCAGCTAATGTAAA	124930
rs35184780	snp	C/G	0.427879	0.175668	intron-variant	ANKRD13B	GRCh38.p7	17:29601604	ATCTGGGATCATTTT[C/G]TTTCCACCTGAAGAA	124930
rs35204464	in-del	-/G			intron-variant	ANKRD13B	GRCh38.p7	17:29607910	CCCAGCCCCACAGCC[-/G]GGGGCCTCCCCAGCA	124930
rs35244918	snp	A/G	0.00230126	0.0338428	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29610753	TTCAGAACAGCACAA[A/G]GGCAAGGTCAAAGGT	124930
rs35416264	in-del	-/T			intron-variant	ANKRD13B	GRCh38.p7	17:29602186	GATCACGAGGTCAGG[-/T]AGATCGAGACCATGC	124930
rs35418248	in-del	-/AC			intron-variant	ANKRD13B	GRCh38.p7	17:29605416	TATATACACACACAA[-/AC]ACACACACACACACA	124930
rs35481781	snp	C/T	0.00523276	0.0508822	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609234	GCTTACCGCGCCCGT[C/T]GTCACCACTCAGCTT	124930
rs35600194	in-del	-/T			intron-variant	ANKRD13B	GRCh38.p7	17:29599865	TTAGCATCTAATTTG[-/T]TTTTTTTTTTTTTTT	124930
rs35831588	in-del	-/T	0.5	0	intron-variant	ANKRD13B	GRCh38.p7	17:29600923	AAATATTTTACTGAC[-/T]TTTTTTTTTTTTTTT	124930
rs35876636	in-del	-/A			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29599387	AGAGCCTGGCAACCG[-/A]GGGAGCAGCAAAGAG	124930
rs36001900	in-del	-/G			downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614659	GACACAAAGAGGGAT[-/G]GGAAGAAAAGAACAA	124930
rs56350121	snp	A/G			upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29593034	GTGCAGACCCTCTTC[A/G]GCCACCTGCCACCCC	124930
rs56988993	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29606722	ATAGTGAGACCCTGT[C/T]TCAAGTAAAAAAAAA	124930
rs57453204	snp	A/C	0.00795532	0.062565	intron-variant	ANKRD13B	GRCh38.p7	17:29597099	CTCGTGGGCTGGGGA[A/C]GGGGCTGAGCAGGCA	124930
rs57541684	snp	A/T	0.5	0	intron-variant	ANKRD13B	GRCh38.p7	17:29606759	AAAAAAAAAAAAAAA[A/T]ATCTTTTGTCTGGGC	124930
rs58154361	snp	A/C	0.0248432	0.108648	intron-variant	ANKRD13B	GRCh38.p7	17:29611208	CTACCTCACAGGGGA[A/C]CAACATGAAATCATG	124930
rs58200244	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29600090	ACCGTGTTAGCCAGG[A/G]TGGTCTCGATCTCCT	124930
rs58659678	snp	C/T			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597632	AGCTAGAGGCCTCTG[C/T]TGAGGAGAAGCTGGA	124930
rs59887630	in-del	-/CTTGCCAC			intron-variant	ANKRD13B	GRCh38.p7	17:29611107	AGAAAGTCAGGGGAC[-/CTTGCCAC]AGATTCTGTATGCCC	124930
rs60464414	in-del	-/TTTTTTTTTT			intron-variant	ANKRD13B	GRCh38.p7	17:29599885	TTTTTTTTTTTTTTT[-/TTTTTTTTTT]GATACGGAGTCTCGC	124930
rs61476683	in-del	-/A			intron-variant	ANKRD13B	GRCh38.p7	17:29602395	TGAGATTCCATCTCA[-/A]AAAAAAAAAAAAAAA	124930
rs62068576	snp	C/G	0.474544	0.10991	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597550	GGGATAAGGAATCTC[C/G]GTTCTCTTGGTGGGG	124930
rs62068577	snp	G/T	0.475081	0.108804	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597860	GAGGAGCACCCTGCT[G/T]GCAAGGAAGTGCCAG	124930
rs62068578	snp	A/G	0	0	intron-variant, utr-variant-5-prime	ANKRD13B	GRCh38.p7	17:29599444	GGGGGGGCAACAGCT[A/G]CAAGGTAGTGGAAAC	124930
rs62068579	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29606017	TCCCGGGTTCAAGCG[A/G]TTCTCTTGCCTCAGC	124930
rs62068580	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29606023	GTTCAAGCGGTTCTC[C/T]TGCCTCAGCCTCCTG	124930
rs71138837	in-del	-/A	0.496105	0.0439572	intron-variant	ANKRD13B	GRCh38.p7	17:29603878	AAAAAAAAAAAAAAA[-/A]GAAAGAAAATATAAC	124930
rs71371123	snp	A/G	0.0107246	0.0724382	intron-variant	ANKRD13B	GRCh38.p7	17:29599496	TTGGAGGCAGAGCCT[A/G]CAAGTTTTTCTGATG	124930
rs71371124	snp	A/G	0.5	0	intron-variant	ANKRD13B	GRCh38.p7	17:29600182	CACCCAGCCGTCTTA[A/G]CATCTAATTTGTATG	124930
rs71376569	snp	A/G	0.5	0	intron-variant	ANKRD13B	GRCh38.p7	17:29600062	TTTGTATTTTTAGTA[A/G]AGACGGGGTTTCACC	124930
rs73278696	snp	G/T	0.0103295	0.0711199	intron-variant, utr-variant-5-prime	ANKRD13B	GRCh38.p7	17:29594429	CTGCGCACCAGGTGG[G/T]CTCCCTGGTTTCTGC	124930
rs73280605	snp	A/G	0.0150606	0.0854603	intron-variant	ANKRD13B	GRCh38.p7	17:29600590	CCTGTGGTGAGGAAG[A/G]GGGGCATCTCCCAGC	124930
rs73280611	snp	C/G	0.0573587	0.15934	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29615224	CTCTGCAGCAAACGG[C/G]TTGTGTATGTGTCTG	124930
rs74267071	in-del	-/AA			intron-variant	ANKRD13B	GRCh38.p7	17:29601776	AGAGAAAAAAAAAAA[-/AA]GAATTCTAGGTTGAA	124930
rs74481278	snp	A/G	0.0244538	0.107838	intron-variant	ANKRD13B	GRCh38.p7	17:29609722	AGTCCTTTCCTTGGC[A/G]TCCCATTTACTCTTC	124930
rs74534021	snp	C/T	0.021333	0.101051	intron-variant	ANKRD13B	GRCh38.p7	17:29601644	ACATTTCCTGCACAT[C/T]TGGCAATAAATTCCC	124930
rs74772596	snp	A/C/G	0.0170614	0.0910698	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598190	AGGGGCCACAGCTCA[A/C/G]AGGCCAACAGGGGCC	124930
rs75662431	snp	A/G	0.0130921	0.0798413	intron-variant	ANKRD13B	GRCh38.p7	17:29595666	GAAACAAGGTCCCAG[A/G]TTCACCCCTACCCCT	124930
rs75784428	snp	A/G	0.0295035	0.117819	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29599387	TAGAGCCTGGCAACC[A/G]GGGAGCAGCAAAGAG	124930
rs75933092	snp	A/G			upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592923	AGGCAAAATGCCAGC[A/G]GGGGAGGTGCGTCCC	124930
rs76015836	snp	A/C	0.5	0	intron-variant	ANKRD13B	GRCh38.p7	17:29602396	TGAGATTCCATCTCA[A/C]AAAAAAAAAAAAAAA	124930
rs76427692	snp	A/C	0.5	0	intron-variant	ANKRD13B	GRCh38.p7	17:29602395	GTGAGATTCCATCTC[A/C]AAAAAAAAAAAAAAA	124930
rs76738011	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29600883	TCATCTGCTGACATC[C/T]CTTCTCTTTATTCTT	124930
rs76837021	snp	C/T	0.00953873	0.0683987	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29591778	TCAACCGCGCCAGCC[C/T]CCTCCCCTGCACTGG	124930
rs77231603	snp	A/C	0.5	0	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29613015	AGGATCCTGTCTCCC[A/C]TAAGCCAGGACACAG	124930
rs77506374	snp	C/T	0.0103295	0.0711199	intron-variant	ANKRD13B	GRCh38.p7	17:29595040	TGGGTGGCCACTTCC[C/T]GTTACCTGTGCCTAT	124930
rs77960128	snp	A/G	0.0298908	0.118541	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597945	TGGAGCCCTGAGGCC[A/G]GGCAGCGGCCTGCCA	124930
rs78169718	snp	C/T	0.0569829	0.158885	intron-variant	ANKRD13B	GRCh38.p7	17:29605058	TACTGAGTTTCACTA[C/T]ACACATGTGAAGTTT	124930
rs78361036	snp	C/T	0.00318978	0.0398085	intron-variant	ANKRD13B	GRCh38.p7	17:29602579	TCTAGTCTCTGCCTC[C/T]GTCTTCACATGGCCT	124930
rs78918512	snp	C/T	0.00119737	0.0244387	intron-variant	ANKRD13B	GRCh38.p7	17:29606430	TGGCATAGTGGTGCT[C/T]GCCTGTAATCCCAGC	124930
rs78990004	snp	A/G	0.0146672	0.084371	intron-variant	ANKRD13B	GRCh38.p7	17:29611164	CTCTGGGTACCAGAT[A/G]CCGTGTCCGAGGTGA	124930
rs79415967	snp	C/T	0.0267878	0.112589	intron-variant	ANKRD13B	GRCh38.p7	17:29608561	CACTCAGTAGGTGTT[C/T]CATAAATATTTGTTG	124930
rs79449326	snp	A/G	0.0111196	0.0737302	intron-variant	ANKRD13B	GRCh38.p7	17:29596335	AAGGGGCACCCAGCA[A/G]TGCTGTGATGCCAGC	124930
rs79823758	snp	C/T	0.0174175	0.0916809	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592750	TTGGTACTGATGCCC[C/T]ACACCTTTCTCAGGA	124930
rs79872689	snp	A/G	0.134802	0.221877	intron-variant	ANKRD13B	GRCh38.p7	17:29594769	CTGGGGGTGGTTAGC[A/G]CAGTTGCCCGCTGTG	124930
rs79996304	snp	C/T	0.0998734	0.199905	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614493	GACTCTAAAACCCTT[C/T]ATCCAATGGTGCTAA	124930
rs80035288	snp	A/G	0.0433465	0.140692	intron-variant	ANKRD13B	GRCh38.p7	17:29610988	GTTCAGTGGAGAGCC[A/G]TGCTGCAAGTGATTA	124930
rs80181893	snp	C/T	0.0074412	0.0605411	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29607837	TGTGCTCCTGGCGCA[C/T]GGCGCAGACGTGGGC	124930
rs80290325	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592766	ACACCTTTCTCAGGA[A/G]TTCCCAATCAGACGC	124930
rs111430893	snp	G/T	0.5	0	intron-variant	ANKRD13B	GRCh38.p7	17:29601056	CAGCCTCCCAGTAGC[G/T]GGGACGATAGGCATG	124930
rs111487344	snp	G/T	0.5	0	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614765	CTTCATACCGGAGGC[G/T]TTTGCTACCTAACTT	124930

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