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
rs410792	snp	C/T	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449363	TTCATGCTAAAAACT[C/T]TCAATAAATTAGGTA	143279
rs1329652	snp	C/T	0.340559	0.233022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486390	TAATAATTCTTGGCG[C/T]TGTTTTGTGGTTGTA	143279
rs1360187	snp	C/T	0.34101	0.232846	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91501045	GGAATGGTGAGCTTC[C/T]ATATACGTATTAGAC	143279
rs2068724	snp	A/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412008	AACCTATTCATCTCA[A/T]AACTGAAAAATTGCC	143279
rs2068725	snp	C/G	0.0244538	0.107838	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412217	TGCTAAAGGGAAAAA[C/G]TCAGTAGCGTCATGT	143279
rs2068866	snp	C/T	0.290201	0.246747	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488632	ATTTATGCTTTAGGA[C/T]TCTTTTTATACTCTT	143279
rs2421517	snp	A/C	0.243633	0.249919	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461843	ATACAAGCCATCACA[A/C]CCAGCCCTTAAATGT	143279
rs2631678	snp	A/C			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91413527	agaaattctgattta[A/C]caatactgcatttgg	143279
rs3834407	in-del	-/GA	0.375	0.216506	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91487103	ATTTTCATAACCTTT[-/GA]TTATAATGTGTAATT	143279
rs3834408	in-del	-/A	0.144296	0.226554	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91512698	GGGAAAGCAAAGTAC[-/A]GTGAAGAATGAATTT	143279
rs4376822	snp	A/G	0.298144	0.245321	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91480409	GGGTTTTGTTTTTCA[A/G]TCCAGGACCCAGTTA	143279
rs4405220	snp	A/G	0.00331674	0.0405878	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91488249	AGAAATATGCCCAAA[A/G]AAGGTGAAAGATGTT	143279
rs4415665	snp	A/G	0.336017	0.234736	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430834	ttgactctttatcca[A/G]tttgccagtctgtgt	143279
rs4537674	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91428335	AGCTTTGTTCTTTTG[A/G]CTTAGGATTGACTTG	143279
rs4537675	snp	A/G	0.299158	0.245119	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91428403	aagtagttttttcca[A/G]ttctgtgaagaaagt	143279
rs4567363	snp	A/C	0.337386	0.23423	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431208	tgttgaatattggcc[A/C]ccactctcttctggc	143279
rs4590777	snp	G/T	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436156	CTTTTGTCTGTTTGT[G/T]TTGGTCTCTGTCCTC	143279
rs5786959	in-del	-/A	0.0271762	0.113356	utr-variant-3-prime, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91513341	ATCACCAGTTGTACC[-/A]AAAACACTAATTTTT	143279
rs6583775	snp	C/T	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457300	ggaacacttcttttt[C/T]gttttacaaagctgg	143279
rs6583776	snp	C/T	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91459489	tggaatactattaag[C/T]aataaaaatgaacta	143279
rs6583777	snp	C/T	0.340784	0.232934	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91495399	TTACACCTTAGCAAA[C/T]TGAAATTTTGGTGGT	143279
rs7071064	snp	A/T	0.139225	0.224118	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458854	acaccaaaagtacaa[A/T]ccataagagaaaaat	143279
rs7072087	snp	G/T	0.340333	0.233109	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482429	CAGAAGCTGTATGTG[G/T]TTCTCCCCTTGTTCT	143279
rs7074559	snp	C/G	0.243347	0.249911	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509048	caaacaccgcatatt[C/G]tcactcataggtggg	143279
rs7075344	snp	A/G	0.325563	0.238307	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91509692	agaaaaccaaatacc[A/G]catattcttacttgt	143279
rs7075424	snp	A/G	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91468865	cacttgagcccagga[A/G]ttcaaaactgtggtg	143279
rs7076784	snp	A/G	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432419	ATGCCTGTCAAATTG[A/G]CTGTCCTTTTAAAAA	143279
rs7076967	snp	G/T	0.0267878	0.112589	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91409445	ATCTCTAACATAAAC[G/T]GAAAGGAACAAGGAA	143279
rs7077014	snp	C/G	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432299	TCTAACAGCTTGTTT[C/G]CCCGTCTGATCTTCA	143279
rs7081363	snp	A/G	0.325327	0.238382	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410192	GAGCCCCGGGCGGGC[A/G]GGGGAGGCGAGAGCA	143279
rs7081569	snp	C/G	0.000309885	0.0124437	missense, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410493	CTGGTGGTGGCGGCG[C/G]CCGCGCCTGAGGAGA	143279
rs7081707	snp	A/G	0.138886	0.22395	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433203	TAACTGTTCCTATGG[A/G]AAGAGTTATTTTTTC	143279
rs7085276	snp	A/T	0.305685	0.24372	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91493796	TTTAAGGCATTTTTT[A/T]AAAAAAATCAAAGTA	143279
rs7087338	snp	C/G	0.139225	0.224118	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458930	agaccctgtgcagag[C/G]atgaaaagacaggct	143279
rs7093711	snp	A/T	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91502533	AGTAATCACACATGG[A/T]AAGTGCCCAATAGCT	143279
rs7098874	snp	C/T	0	0	upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91410013	CCCGACTGCCCGTCC[C/T]TAGTCCAGGTTCTCC	143279
rs7100516	snp	A/C	0.145305	0.227022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497398	caggtccgagcaatt[A/C]tcctgcctcagcctc	143279
rs7100786	snp	A/G/T	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497484	ttttttttttttttg[A/G/T]atttttagtagagac	143279
rs7342052	snp	A/G	0.340559	0.233022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91432826	GTTTTTACACCCCCT[A/G]GAGAAAAGCATACTG	143279
rs7476690	snp	G/T			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437641	tttttttttttttgg[G/T]tgttttgtttttttt	143279
rs7478184	snp	C/T	0.34146	0.23267	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91510215	CTAAAAGGGCATGAA[C/T]CCTTGGCAATATTTT	143279
rs7894248	snp	C/T	0.340333	0.233109	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476506	CCAGACTAAGAAGCC[C/T]CTAGGCTTCTCAGAA	143279
rs7895635	snp	A/C	0.139903	0.224452	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91450691	caagaaaaaaaaaaa[A/C]catcaaaaagtgggc	143279
rs7895666	snp	C/T	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471636	aatgcaaaatcaata[C/T]ataaaaatcagtagc	143279
rs7898769	snp	A/T	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91417470	tggtgtgctgcaccc[A/T]ttaactcatcattta	143279
rs7898845	snp	A/T	0.340333	0.233109	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91480947	TATTTTCAGCATATT[A/T]TGGACTGTCTCAATA	143279
rs7899190	snp	G/T	0.00514135	0.0504405	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91494865	ATCACAATTTAGATT[G/T]GGATGATATTTTGAC	143279
rs7899549	snp	A/G	0.140242	0.224618	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91451130	ccaacccaaatgccc[A/G]tcaatgatagactgg	143279
rs7900774	snp	A/G	0.326976	0.237854	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91491711	GAGGTCTGACCTACA[A/G]GGTATATTGGGTCTA	143279
rs7904419	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415393	AGATATTACAAATAT[A/G]CAAAATAAGTGTTTA	143279
rs7904917	snp	C/T	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91415632	TAACAGAGATGTTTC[C/T]GACTCATGTTCTTTG	143279
rs7906306	snp	C/T	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431688	ggctcctgaggcttc[C/T]gcattcttcacgtgg	143279
rs7907010	snp	G/T	0.347914	0.230028	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91458015	gcagatggcataatt[G/T]tctatgcaaaaaaaa	143279
rs7908457	snp	A/G	0.340333	0.233109	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91476242	caaatgaagggattg[A/G]ccttggtcaagtgca	143279
rs7908769	snp	C/T	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91437169	ttttattcacaaata[C/T]gtaatttgtgtggag	143279
rs7910115	snp	A/G	0.190519	0.242821	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433979	AACTTTATAGAGAGG[A/G]GACTTTCAAATATTT	143279
rs7910297	snp	A/G	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471440	actcttagcactcct[A/G]ttcaacatagtactg	143279
rs7914133	snp	C/T	0.340559	0.233022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485851	CATTTCTCATTTCTT[C/T]TGTAAGAAAAAGTGG	143279
rs7914794	snp	C/T	0.340559	0.233022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91486315	ATATTTTCTTGGCAA[C/T]GTTTACTTTACAAAG	143279
rs7916523	snp	G/T	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91421403	TCCTTATATTATCAG[G/T]TGTGTCCAATCTTTT	143279
rs7918822	snp	A/G	0.0283406	0.115616	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91466188	ttcagtaacatatct[A/G]ggttatcaaatttgt	143279
rs7919792	snp	C/T	0.202651	0.245475	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91490933	aaGAGATGAGACATA[C/T]GGAAACTGTGATGCA	143279
rs7919797	snp	C/G	0.338976	0.23363	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91430769	attttgagcccatgt[C/G]tgtctctgcatgtgc	143279
rs7920553	snp	C/T	0.242488	0.249887	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91511950	ACTCGAACAAGACCC[C/T]ACAGCTAGTAAGTGG	143279
rs7920604	snp	A/G	0.17366	0.238059	synonymous-codon, intron-variant, nc-transcript-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91461320	TTTTTATCTAACAAC[A/G]TTTGATTCTTTCCCA	143279
rs7920790	snp	A/G	0.340559	0.233022	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431613	taaacttcccttctc[A/G]cttcatttcattcat	143279
rs9651433	snp	A/G	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91420466	TGGTGGCATGTGCCT[A/G]TAATCCCAGCTACTC	143279
rs9664423	snp	A/C/G	0.0655868	0.168795	intron-variant, utr-variant-3-prime	HECTD2, HECTD2-AS1	GRCh38.p7	10:91462266	AATATTGTAAAAATC[A/C/G]CCTTATAATTACCTT	143279
rs9732191	snp	A/T	0.338976	0.23363	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91456354	tgtgaatgggagttc[A/T]ctcatgatttggctc	143279
rs9732307	snp	C/G	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439217	ggttttaggtttaat[C/G]cttaagtctttaatt	143279
rs9732335	snp	A/C	0.0244538	0.107838	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91439397	attgtagatgtgtgg[A/C]attatttctgagacc	143279
rs9761396	snp	G/T	0.375	0.216506	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91449254	TGGATTACGTTTATT[G/T]ATTTGTGTATGTTGA	143279
rs9804186	snp	A/G	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438163	AGGTATACACGTGCA[A/G]TGGTGGTTGCCTGCA	143279
rs9804311	snp	C/T	0.34146	0.23267	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91438314	TTCAACTGCCACTTA[C/T]GAGTGAGAACATGCA	143279
rs9943307	snp	A/G	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91444679	CTGTTCTCACAGATG[A/G]TTCTTAAAATATAAT	143279
rs10450389	snp	A/G	0.00597247	0.0543191	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91433492	tttctgtatcagtac[A/G]tagaaaacttcttta	143279
rs10786000	snp	C/G	0.00914312	0.0669923	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91414920	AGTGGGAAGCTATTG[C/G]AATTTCTGAAACAGA	143279
rs10786001	snp	A/G	0.0178098	0.0926698	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470986	GAGACACACACACAC[A/G]CACGCACACACACAC	143279
rs10881915	snp	C/T	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91497091	cagcctcctgagtat[C/T]tgggattttaggcat	143279
rs11186558	snp	A/G	0.316726	0.240931	intron-variant, upstream-variant-2KB	HECTD2-AS1, HECTD2	GRCh38.p7	10:91407751	ACCCTATTCCCCATA[A/G]GTATAATTAATGAGC	143279
rs11186559	snp	A/C			upstream-variant-2KB, intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91408290	CTTGCCTTGTTTTGC[A/C]AATATTTAAGCAGTT	143279
rs11186560	snp	C/T	0.340333	0.233109	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91411010	CTTCGCTTTTCTTTC[C/T]CTTCCCCCTTCAGAT	143279
rs11186561	snp	A/G	0.00793638	0.0624916	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91412666	ACAGGATCTGTGGCA[A/G]AAtgtgtgtgtgtgt	143279
rs11186562	snp	A/G	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91416019	TTAAACCACAAAGCC[A/G]TAAAGTCTCTTTGTC	143279
rs11186563	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91418583	TGTACCTTGAAAGTA[A/G]CTGACTTTTCATATC	143279
rs11186565	snp	C/T	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91423701	TAATTCTAGAGACTT[C/T]TTAATTCTATGTGTA	143279
rs11186567	snp	A/G	0.190519	0.242821	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91431670	CTTCCAGTTGATCGC[A/G]TCGGCTCCTGAGGCT	143279
rs11186570	snp	A/G	0.340333	0.233109	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91436326	TAGCCTGTTGATTGA[A/G]GAACCCTGATGTCCG	143279
rs11186571	snp	C/T	0.298905	0.24517	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91443496	TGCCAGCTGGAGCTC[C/T]CCTGTATGTGGTGTT	143279
rs11186572	snp	C/T	0.175897	0.238765	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91445618	GAATAGGAACAGCTC[C/T]GGTCTGCAGCTCCCA	143279
rs11186573	snp	C/G	0.340108	0.233197	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91453218	AGGAGGATGGCCTGA[C/G]GCCAAGAGTTTGAGA	143279
rs11186574	snp	A/G	0.157972	0.232445	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91457844	TCTTAATGGCTAAAG[A/G]CTTAGTGCTTTCCCT	143279
rs11186575	snp	C/T	0.192088	0.2432	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91460347	CATTTGTTTTCTGTT[C/T]ATGTTGAATTAATCT	143279
rs11186577	snp	A/G	0.00716266	0.059414	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91470994	CACACACACACGCAC[A/G]CACACACAGACACAC	143279
rs11186578	snp	C/G	0.0023933	0.0345097	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471003	ACGCACACACACACA[C/G]ACACACACGCACACA	143279
rs11186579	snp	A/G			intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91471016	CAGACACACACGCAC[A/G]CACACAAAGAAAACC	143279
rs11186580	snp	C/T	0.340784	0.232934	intron-variant, upstream-variant-2KB	HECTD2, HECTD2-AS1	GRCh38.p7	10:91482066	AAACATATGTAGAGA[C/T]AGTAAAAGCTAGAAA	143279
rs11186581	snp	C/G	0.0138799	0.0821421	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91483869	AACTCACGGCTAGCA[C/G]CACTGTAACTCATGC	143279
rs11186582	snp	G/T	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485519	TTTTGGTTTGGTTAA[G/T]AGCATCTTTTCAAGA	143279
rs11186583	snp	A/T	0	0	intron-variant	HECTD2, HECTD2-AS1	GRCh38.p7	10:91485582	TATCTCTTACTATTC[A/T]ATGCAcaggggtcag	143279

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