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
rs701378	snp	C/T	0.441977	0.16014	utr-variant-3-prime	CORO2A	GRCh38.p7	9:98122860	CAGTTCTGAAGTCTG[C/T]GTCCCTCCATAAGGG	7464
rs701379	snp	A/T	0.439085	0.163545	utr-variant-3-prime	CORO2A	GRCh38.p7	9:98124543	TAATAACAGAATTCA[A/T]CAGAAGGCATCATCT	7464
rs715910	snp	C/T	0.399611	0.200291	intron-variant	CORO2A	GRCh38.p7	9:98149229	aacaacaaatCGTTA[C/T]TTTTGCTTTTTTCtt	7464
rs735111	snp	A/G	0.173399	0.23798	synonymous-codon	CORO2A	GRCh38.p7	9:98133161	AAGCCCCATGAGTAC[A/G]ATTAGCTGTCACCAA	7464
rs751800	snp	A/C	0.235273	0.249566	utr-variant-3-prime	CORO2A	GRCh38.p7	9:98122282	GTGGAGCTTATATGA[A/C]CATACAGGCCCTACT	7464
rs753991	snp	C/G	0.0759472	0.179459	utr-variant-3-prime	CORO2A	GRCh38.p7	9:98123010	GCAAACCCAGATCAC[C/G]CCACAGGTAGTTTTC	7464
rs774121	snp	C/T	0.40263	0.198	intron-variant	CORO2A	GRCh38.p7	9:98143706	ACCATTACCCAGTTT[C/T]ATTGTTGCTCAGTAT	7464
rs774122	snp	A/G	0.3746	0.216737	intron-variant	CORO2A	GRCh38.p7	9:98149448	gaatatgtgaggctg[A/G]gtatttacaaagaaa	7464
rs774123	snp	A/T	0.398534	0.201091	intron-variant	CORO2A	GRCh38.p7	9:98149568	atcatgcagacagtg[A/T]aggggggatcaggtg	7464
rs774124	snp	A/G			intron-variant	CORO2A	GRCh38.p7	9:98190931	CCATGGCCGCAGGGC[A/G]AGGTCATAGGCACTA	7464
rs812280	snp	A/G	0.5	0	intron-variant	CORO2A	GRCh38.p7	9:98154329	cttatgtgTTTGTGt[A/G]tatatatatatatat	7464
rs814027	snp	C/T	0.444	0.157683	intron-variant	CORO2A	GRCh38.p7	9:98149389	ATGAGAAGCTCTGAT[C/T]AGTGGCTCCTGGGtg	7464
rs882265	snp	C/T	0.0228947	0.104514	intron-variant	CORO2A	GRCh38.p7	9:98157761	TTGAACTGACCACTG[C/T]CCTGCTCGTACCCTC	7464
rs942164	snp	C/T	0.0551013	0.156571	utr-variant-3-prime	CORO2A	GRCh38.p7	9:98122752	CCTGGGGGACTCTTC[C/T]GTTAACTAGGGCTGA	7464
rs942165	snp	G/T	0.2768	0.248559	intron-variant	CORO2A	GRCh38.p7	9:98127058	TGTAGGAACAGCACG[G/T]TGCGTGCACTGAAGC	7464
rs1063628	snp	A/C	0	0	utr-variant-3-prime, upstream-variant-2KB	CORO2A, TRIM14	GRCh38.p7	9:98121238	CTTTGGCAGGTATCC[A/C]CCTTAACGCTACAAT	7464
rs1201535	snp	G/T	0.4021	0.198407	intron-variant	CORO2A	GRCh38.p7	9:98143774	ACAAACTGTTCTGCA[G/T]GGGGACTCCCATCCT	7464
rs1539288	snp	C/G	0.492918	0.0590819	intron-variant	CORO2A	GRCh38.p7	9:98168803	AGCATGAAGCAGCCT[C/G]CCAGGGGCCAAGTGG	7464
rs1539289	snp	C/T	0.487368	0.0784625	intron-variant	CORO2A	GRCh38.p7	9:98168831	TGGCTCGTGAGAGTT[C/T]CAACCCCTGGTGCAA	7464
rs1539290	snp	A/G	0.167158	0.235875	intron-variant	CORO2A	GRCh38.p7	9:98168876	GAAACAGACACACAC[A/G]TGCAGAAGGCTAGCT	7464
rs1544204	snp	C/G	0.287085	0.247234	intron-variant	CORO2A	GRCh38.p7	9:98160405	AGACCTCAGATTTGG[C/G]TCTGAGCTTCCTAGT	7464
rs1544205	snp	A/G	0.259674	0.249813	intron-variant	CORO2A	GRCh38.p7	9:98160592	AAATGACCTCCCTAG[A/G]GTCTTGGCAACTTGG	7464
rs1746239	snp	C/T	0.455181	0.142831	utr-variant-3-prime	CORO2A	GRCh38.p7	9:98123497	CTATTCTCTCTCTCt[C/T]ttttttttttttttt	7464
rs1891322	snp	C/T	0.449091	0.151204			GRCh38.p7	9:98160338	AGAGATCACCTGAAA[C/T]GCAGGAGGAGTTAAG	7464
rs1891323	snp	A/G	0.0554779	0.157039			GRCh38.p7	9:98122656	CTACTTCTTTACCTC[A/G]TATAGTCATTTCAGA	7464
rs1977261	snp	A/G	0.49168	0.063958	upstream-variant-2KB, intron-variant	CORO2A	GRCh38.p7	9:98174098	ggcaacgagagtgaa[A/G]ctctgtTCCCCCGCC	7464
rs1983815	snp	A/C	0.312104	0.242163	intron-variant	CORO2A	GRCh38.p7	9:98175828	aatggggatgataac[A/C]ataaatgagttaata	7464
rs1985859	snp	C/T	0.440195	0.162252	upstream-variant-2KB, intron-variant	CORO2A	GRCh38.p7	9:98173831	TAAGAGCGTGTAGCC[C/T]TTGGTCTGGGTGTGG	7464
rs2050982	snp	G/T	0.00557542	0.0525036	intron-variant	CORO2A	GRCh38.p7	9:98140710	ttgccctcctaaagt[G/T]agggattacaggcat	7464
rs2050983	snp	G/T	0.370974	0.218781	intron-variant	CORO2A	GRCh38.p7	9:98140965	aacattaaacttata[G/T]aagttgataatgtac	7464
rs2093697	snp	A/C			intron-variant	CORO2A	GRCh38.p7	9:98157097	TAGCTAGTTTTGACT[A/C]AATGTTTGTTTCCCT	7464
rs2181580	snp	C/T	0.452473	0.146644	intron-variant	CORO2A	GRCh38.p7	9:98167052	GAGGCTGCAGTAAGC[C/T]ATGATTATACCACTG	7464
rs2181581	snp	C/T	0.466824	0.124448	intron-variant	CORO2A	GRCh38.p7	9:98187927	AGTTTCAATAAGCCA[C/T]GTAACTTTTCTGTAT	7464
rs2231652	snp	C/G	0.249603	0.25	upstream-variant-2KB, intron-variant	CORO2A	GRCh38.p7	9:98173472	AGTGCTCATGGAGCC[C/G]GTGGATTTTGGACAG	7464
rs2231653	snp	C/T	0.117537	0.212022	upstream-variant-2KB, intron-variant	CORO2A	GRCh38.p7	9:98173391	CTCTGCAGAGTGCCC[C/T]GGCCACACTCACGAA	7464
rs2231654	snp	A/G	0.0733688	0.176922	upstream-variant-2KB, intron-variant	CORO2A	GRCh38.p7	9:98173244	GGCTTCCTAGTCACC[A/G]GGAACTTGGTGGAAG	7464
rs2231655	snp	C/T	0.00517822	0.0506191	upstream-variant-2KB, intron-variant	CORO2A	GRCh38.p7	9:98173185	ccgaatcagaaactc[C/T]agggtggggcccaac	7464
rs2231656	snp	C/T	0.144632	0.226711	upstream-variant-2KB, intron-variant	CORO2A	GRCh38.p7	9:98172939	CATGTAAATGTGATG[C/T]TGTCACCTGTCCTCA	7464
rs2231657	snp	A/G/T	0.0821764	0.185298	intron-variant	CORO2A	GRCh38.p7	9:98157777	TGCATCACCGTCCAC[A/G/T]TTGAACTGACCACTG	7464
rs2231658	snp	A/C/G	0.000148251	0.00860852	missense	CORO2A	GRCh38.p7	9:98137652	TACCCAAAAGTCTGC[A/C/G]GGCACAGAGGCAACG	7464
rs2231659	snp	C/G/T	0.00271441	0.0367402	missense, synonymous-codon	CORO2A	GRCh38.p7	9:98137647	AAAAGTCTGCGGGCA[C/G/T]AGAGGCAACGTTTTG	7464
rs2231660	snp	A/G/T	0.000780795	0.0197433	missense	CORO2A	GRCh38.p7	9:98134880	GAACTCGTGGGCCAC[A/G/T]CGCGCAGAGTAGGCC	7464
rs2231661	snp	A/G	0.0325976	0.123435	intron-variant	CORO2A	GRCh38.p7	9:98133277	TCCTGGCCAGCATGT[A/G]ACTATGAGGCCCAGG	7464
rs2231662	snp	C/T	0.0146011	0.0841865	intron-variant	CORO2A	GRCh38.p7	9:98132170	GGTGAGGGCTGCACC[C/T]CACCCCTCACCATCA	7464
rs2231663	snp	C/G	0.0217236	0.101931	intron-variant	CORO2A	GRCh38.p7	9:98132018	ATGCTGACAGCCCCG[C/G]GCGAGCCCAGACCCT	7464
rs2231664	snp	A/C/T	0.0226052	0.103884	intron-variant	CORO2A	GRCh38.p7	9:98130926	GGGAGGGAGGTGACC[A/C/T]CCTGGACCCCTGAGA	7464
rs2231665	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2A	GRCh38.p7	9:98130848	GGGCAGGCCTCGCTG[A/G]CCACTCTTTCCCTGT	7464
rs2231666	snp	A/G	0.000115391	0.00759487	missense	CORO2A	GRCh38.p7	9:98129874	GAGATGGCAACATCC[A/G]CTACTACGAGGTGAG	7464
rs2231667	snp	C/T	0.021333	0.101051	intron-variant	CORO2A	GRCh38.p7	9:98129708	GTCAGGGCTTCAGTG[C/T]GGGGTCTGGGGAGAC	7464
rs2231668	snp	A/G/T	0.00505293	0.05001	intron-variant	CORO2A	GRCh38.p7	9:98128121	TGACAGGAACATGGC[A/G/T]TGCCCAGTGGCCCCA	7464
rs2231669	snp	A/G/T	0.0498117	0.149749	intron-variant	CORO2A	GRCh38.p7	9:98126863	TATGCCCATCTTCCC[A/G/T]TGGGCACCCCGTCCT	7464
rs2231670	snp	C/T	0.0143654	0.0835245	intron-variant	CORO2A	GRCh38.p7	9:98126835	CCTCACATGGCTCTG[C/T]TTCCCTTCCAGACCC	7464
rs2231671	snp	A/G	0.0221141	0.102801	intron-variant	CORO2A	GRCh38.p7	9:98126421	TGGCCTGGCCTAGTC[A/G]CTTGACTCATTTTGT	7464
rs2231672	snp	A/G	0.0185938	0.0946107	intron-variant	CORO2A	GRCh38.p7	9:98126386	TCATTCAACAAACAG[A/G]CAGTGAGCTCCATCT	7464
rs2250494	snp	A/C	0.498652	0.0259235	intron-variant	CORO2A	GRCh38.p7	9:98157036	AGCAACACTTGCACT[A/C]AGGACAAAAGCCTGT	7464
rs2275709	snp	A/T	0.267636	0.249377	utr-variant-5-prime, intron-variant	CORO2A	GRCh38.p7	9:98172669	TCTGCTCACCCTTAA[A/T]CAGTTCCCCAGGCAG	7464
rs2275710	snp	C/T	0.437259	0.165632	utr-variant-5-prime, intron-variant	CORO2A	GRCh38.p7	9:98172768	ACCTAAATTGTTTGT[C/T]CAGGCTGGGCCTGCA	7464
rs2417732	snp	G/T	0.31357	0.241783	intron-variant	CORO2A	GRCh38.p7	9:98154975	GGTTGGTATTTCTGG[G/T]TCACAGGTATATGCA	7464
rs2417733	snp	A/G	0.364401	0.222289	intron-variant	CORO2A	GRCh38.p7	9:98166700	ATGAAAGCAGGGTCT[A/G]GAAGAGATATTTGCA	7464
rs2476443	snp	C/T	0.351418	0.228505	intron-variant	CORO2A	GRCh38.p7	9:98153999	TAATATGATGATTTA[C/T]CTTTATAGATTTACT	7464
rs2487912	snp	A/T	0.465368	0.126951	downstream-variant-500B, upstream-variant-2KB	CORO2A, TRIM14	GRCh38.p7	9:98120599	CTAGACTTCCACTTA[A/T]AAAGCCCTCAGCTCT	7464
rs2761059	snp	C/G	0.490618	0.0678448	intron-variant	CORO2A	GRCh38.p7	9:98138839	ggatcacgaggtcag[C/G]agatcgagaccatcc	7464
rs2761060	snp	C/T	0.453087	0.145793	intron-variant	CORO2A	GRCh38.p7	9:98147609	atttagcaagtaaaa[C/T]acaggatgcccagta	7464
rs2761061	snp	A/C	0.487746	0.0773096	intron-variant	CORO2A	GRCh38.p7	9:98150564	GGTCCCCTCTCCCAA[A/C]CCACGTCACACTCTA	7464
rs2761062	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2A	GRCh38.p7	9:98171574	CCAGCGCTGCAAGTT[A/G]CAGCAGGGAGATGGA	7464
rs2795486	snp	A/T	0.135825	0.222405	intron-variant	CORO2A	GRCh38.p7	9:98140886	CCCCTACTGGAGGGG[A/T]CAACGctataaagga	7464
rs2795487	snp	C/T	0.431177	0.172264	intron-variant	CORO2A	GRCh38.p7	9:98141897	CAGTAACAGAAGCTA[C/T]TATTATATGTATATG	7464
rs2795488	snp	C/T	0.144969	0.226867	intron-variant	CORO2A	GRCh38.p7	9:98142181	CAGGAATGGAGCCCA[C/T]AGCTGCACTGTCTTA	7464
rs2795489	snp	A/G	0.41507	0.187755	intron-variant	CORO2A	GRCh38.p7	9:98147649	ttgcagataaacaac[A/G]aatattttagcataa	7464
rs2795490	snp	G/T	0.452965	0.145963	intron-variant	CORO2A	GRCh38.p7	9:98147714	atttgtAaaaataaa[G/T]tgacagtttcttata	7464
rs2795491	snp	C/T	0.397452	0.201886	intron-variant	CORO2A	GRCh38.p7	9:98149140	agggtaaaggataca[C/T]agaattgcactgtac	7464
rs2795492	snp	A/G	0.441432	0.160792	intron-variant	CORO2A	GRCh38.p7	9:98151094	CCCTTTGCCATTTAT[A/G]CCCTCCCTATTTATT	7464
rs2795493	snp	A/G	0.444267	0.157354	intron-variant	CORO2A	GRCh38.p7	9:98153534	gcttcagcctctcgt[A/G]tagctgggactacag	7464
rs2795494	snp	A/G	0.470521	0.117772	intron-variant	CORO2A	GRCh38.p7	9:98153620	TGCTATACTGCCCAG[A/G]CTATATGTCTGTAAC	7464
rs2795495	snp	A/T	0.471388	0.116136	intron-variant	CORO2A	GRCh38.p7	9:98154280	gaaagttttgtagga[A/T]ttacctgtaaaacca	7464
rs2985029	snp	C/T	0.45692	0.1403	intron-variant	CORO2A	GRCh38.p7	9:98148134	gcaaggtggttcatg[C/T]ctgtaatcccagctc	7464
rs2985030	snp	A/T	0.139225	0.224118	intron-variant	CORO2A	GRCh38.p7	9:98148212	CCAGCCTGGCCAACA[A/T]AGCAAAACCCCATCT	7464
rs3055383	in-del	-/T/TTT/TTTT	0.301681	0.2446	intron-variant	CORO2A	GRCh38.p7	9:98152126	CTGTTTTTTTTTTTT[-/T/TTT/TTTT]GTTTTTTCTTTAAGG	7464
rs3059554	in-del	-/TT			intron-variant	CORO2A	GRCh38.p7	9:98177480	ttttttttttttttt[-/TT]gagacagagtctggc	7464
rs3174288	snp	A/C/G/T	0.000362402	0.0134565	synonymous-codon, missense	CORO2A	GRCh38.p7	9:98126722	GCCCCAGCCTCACCC[A/C/G/T]GGCTCTTGAATCAGA	7464
rs3758261	snp	A/G	0.238171	0.24972	upstream-variant-2KB, intron-variant	CORO2A	GRCh38.p7	9:98174030	AACCTCCACCTCCCA[A/G]GTTCAAGCAATTCTC	7464
rs3758262	snp	G/T	0.238749	0.249747	upstream-variant-2KB, intron-variant	CORO2A	GRCh38.p7	9:98173958	CGGCTAATTTTGTAT[G/T]TTTAGTAAAGACGGG	7464
rs3758263	snp	C/T	0.145305	0.227022	upstream-variant-2KB, intron-variant	CORO2A	GRCh38.p7	9:98173946	TATTTTTAGTAAAGA[C/T]GGGGTTTCTCCATGT	7464
rs3780456	snp	C/G	0.23846	0.249734	intron-variant	CORO2A	GRCh38.p7	9:98162449	AGAGGATTGGGGGAC[C/G]GACAGAAGGGCACTG	7464
rs3780457	snp	C/T	0.161267	0.233723	intron-variant	CORO2A	GRCh38.p7	9:98160125	TTAGGGCAAAGCTCC[C/T]GAAAGGAGAGTTGGA	7464
rs3780458	snp	A/C	0.377582	0.214995	intron-variant	CORO2A	GRCh38.p7	9:98159920	GTGGGCTGGGTGAGC[A/C]TCTTCTTTATCTTGA	7464
rs3780459	snp	A/T	0.451359	0.148171	intron-variant	CORO2A	GRCh38.p7	9:98146686	TCTCACTTCACTGAC[A/T]TGAGGCCCCTGAGGT	7464
rs3780460	snp	A/G	0.393987	0.204372	intron-variant	CORO2A	GRCh38.p7	9:98144788	GTCCTCCAGCCTACC[A/G]TGCCCGCTGGCTGCT	7464
rs3780461	snp	C/G	0.227074	0.248947	intron-variant	CORO2A	GRCh38.p7	9:98143923	ACTGTGCCCAGCCAA[C/G]AAGCATTTAAAAACC	7464
rs3780464	snp	C/G	0.301932	0.244547	intron-variant	CORO2A	GRCh38.p7	9:98143420	CGTCCTGCCACCCCT[C/G]CCTCCCAGTCTCCAC	7464
rs3780465	snp	C/T	0.230017	0.2492	intron-variant	CORO2A	GRCh38.p7	9:98143376	GATGCTCATTTGAGG[C/T]CATGACTATGATGCT	7464
rs3824454	snp	A/G	0.328382	0.237395	intron-variant	CORO2A	GRCh38.p7	9:98190862	TGTTATTATCCCCTC[A/G]TAAAAGCAGGCAAAG	7464
rs3837264	in-del	-/CGCAGGGCAGCGCAG			intron-variant	CORO2A	GRCh38.p7	9:98142852	GGCAGCGCAGGGCAG[-/CGCAGGGCAGCGCAG]GGCAGGGCAGGGCAG	7464
rs3837265	in-del	-/T	0.297128	0.245518	intron-variant	CORO2A	GRCh38.p7	9:98141939	GCTCATTCCTTTTAG[-/T]TTTTTTTTTCTCAGT	7464
rs3837266	in-del	-/TGGCTTAAGCGT/TGGCTTGAGCGT			intron-variant	CORO2A	GRCh38.p7	9:98141342	aaaaaaaaGGGTCAG[-/TGGCTTAAGCGT/TGGCTTGAGCGT]TGGTCCCATGGAGAC	7464
rs4266764	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2A	GRCh38.p7	9:98171758	CAGGAGCTTGCAGCG[C/T]GGGGGTGGGGAGGCT	7464
rs4610873	snp	G/T	0.489083	0.0730708	intron-variant	CORO2A	GRCh38.p7	9:98171751	ATGGAGCCAGGAGCT[G/T]GCAGCGCGGGGGTGG	7464
rs4742718	snp	A/G	0.441705	0.160466	intron-variant	CORO2A	GRCh38.p7	9:98151964	TGGGACCACAGGCGC[A/G]CGCCACCATGCCCGG	7464
rs4743170	snp	A/G	0.466412	0.125164	intron-variant	CORO2A	GRCh38.p7	9:98138500	acccaaatgcccatc[A/G]agtgaagaatggaca	7464
rs4743171	snp	C/T	0.452227	0.146984	intron-variant	CORO2A	GRCh38.p7	9:98145853	AAGTAGCTGGGACTA[C/T]AGGCATGTGCCACCA	7464

Full records

It may take some time, please wait.