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
rs189197	snp	A/T	0.32627	0.238082	intron-variant	UBE2Q2	GRCh38.p7	15:75894004	TAACTAAGATCAGAG[A/T]ATGACACTGTCCTTT	92912
rs191394	snp	A/G	0.0205511	0.0992634	intron-variant	UBE2Q2	GRCh38.p7	15:75897759	CACATCAGCCCAGGA[A/G]CTTGAGGCTGCAGTC	92912
rs335687	snp	A/G	0.0973687	0.197999	utr-variant-3-prime, nc-transcript-variant	UBE2Q2	GRCh38.p7	15:75899625	AAATGAGCAAAATGC[A/G]AAGGCTGTAACTTAT	92912
rs335688	snp	A/G	0.00666292	0.0573329	utr-variant-3-prime, nc-transcript-variant	UBE2Q2	GRCh38.p7	15:75899511	TTTTGTCTGCATGTT[A/G]GAAAGATTTTCTTTA	92912
rs335689	snp	C/T	0.012886	0.0792272	utr-variant-3-prime, missense, nc-transcript-variant	UBE2Q2	GRCh38.p7	15:75899461	ATACAACAGTCAACA[C/T]ATTTAGCCATCTTCC	92912
rs335690	snp	C/T	0.0383715	0.133092	intron-variant	UBE2Q2	GRCh38.p7	15:75899013	TCCACCTCCCCAAAG[C/T]GCTGGGATTACAGGT	92912
rs335691	snp	A/G	0.029116	0.117091	intron-variant	UBE2Q2	GRCh38.p7	15:75897795	CAGTCCAAGCTACTG[A/G]GGAGACTGAGGCAGG	92912
rs335692	snp	C/T	0.0383715	0.133092	intron-variant	UBE2Q2	GRCh38.p7	15:75897283	CCACTGCACTCCAGC[C/T]GGGGTGACAGAGCGA	92912
rs335708	snp	A/G	0.0678174	0.1712	intron-variant	UBE2Q2	GRCh38.p7	15:75894303	taggattataggagt[A/G]agccactgtccctgg	92912
rs335709	snp	A/G	0.029116	0.117091	intron-variant	UBE2Q2	GRCh38.p7	15:75893518	tcttactagtagtac[A/G]cagggtatgttgaaa	92912
rs335710	snp	C/T	0.170084	0.236883	intron-variant	UBE2Q2	GRCh38.p7	15:75892780	caagtgatcttccca[C/T]ctcagcctcctgagt	92912
rs335711	snp	A/G	0.324145	0.238752	intron-variant	UBE2Q2	GRCh38.p7	15:75892399	ctgtgttctgtatct[A/G]ataattccaaaacct	92912
rs335712	snp	C/T	0.0287284	0.116357	intron-variant	UBE2Q2	GRCh38.p7	15:75891538	TAATAATAGCACCTA[C/T]TTTTTAAGTTATTAA	92912
rs335713	snp	A/G	0.171057	0.237209	intron-variant	UBE2Q2	GRCh38.p7	15:75890608	TTCTTGAAAGTAGAC[A/G]CTATTTTAAAAATAA	92912
rs335714	snp	C/T	0.0205511	0.0992634	intron-variant	UBE2Q2	GRCh38.p7	15:75890255	ATTCTAATGTTATCA[C/T]GCTAATGTAATCCCT	92912
rs335715	snp	A/T	0.324619	0.238604	intron-variant	UBE2Q2	GRCh38.p7	15:75890065	CTTTCTCTACCATGT[A/T]ACAGCCATGAGTTTT	92912
rs335716	snp	C/T	0.0387552	0.1337	intron-variant	UBE2Q2	GRCh38.p7	15:75889393	CATTAATAATTGTTA[C/T]AGTGACAATATTTAA	92912
rs335717	snp	G/T	0.144632	0.226711	intron-variant	UBE2Q2	GRCh38.p7	15:75889181	GGATTAAATTTTTTT[G/T]TGTGTATTCTATTTC	92912
rs963249	snp	A/G	0.009685	0.0689108	intron-variant	UBE2Q2	GRCh38.p7	15:75887582	TACTTAGCAGAGGGG[A/G]AAAAAAAAAAAAAAA	92912
rs1020416	snp	C/T	0.00438332	0.0466095	intron-variant	UBE2Q2	GRCh38.p7	15:75864275	aattactgTGTAAAC[C/T]AGATCTACACCCTAG	92912
rs1039547	snp	C/T	0.0970103	0.197722	intron-variant	UBE2Q2	GRCh38.p7	15:75883969	TTAGGATCACAGGCA[C/T]GTGGGGACCATTCTC	92912
rs1131973	snp	A/T	1.66081e-05	0.00288163	missense, intron-variant, nc-transcript-variant	UBE2Q2	GRCh38.p7	15:75877969	TTAACAGGGATTTAT[A/T]CAGTGGAACTCATAA	92912
rs1183602	snp	A/G	0	0	intron-variant	UBE2Q2	GRCh38.p7	15:75885910	TCATGATCAGTTTTG[A/G]AAGTGGAATGTTAGG	92912
rs1183603	snp	A/G/T	0.000399281	0.0141238	intron-variant	UBE2Q2	GRCh38.p7	15:75885966	CAAAATAAACACAAG[A/G/T]CTGAAAAATAGTAAA	92912
rs1185088	snp	G/T	0	0	intron-variant	UBE2Q2	GRCh38.p7	15:75886115	GAAATGACATAACTA[G/T]TGTGTTTTAGttttt	92912
rs1394123	snp	A/G	0.029116	0.117091	intron-variant	UBE2Q2	GRCh38.p7	15:75878862	AATCTAATCTAGTAA[A/G]GGAGTTCAGAGTTTG	92912
rs1394124	snp	A/T	0.029116	0.117091	intron-variant	UBE2Q2	GRCh38.p7	15:75878817	GAAAATAGTCACATG[A/T]ATATAATTTTCTCAA	92912
rs1394125	snp	A/G	0.379942	0.213577	intron-variant	UBE2Q2	GRCh38.p7	15:75866642	ACTTACATCTCTTCT[A/G]TTTTCTCCCCCATCT	92912
rs1394126	snp	A/G	0.0487975	0.148383	intron-variant	UBE2Q2	GRCh38.p7	15:75866754	TCTGGCCCTTCTACA[A/G]GTGGTTTTTTGGGGG	92912
rs1532783	snp	C/T	0.0614824	0.164198	intron-variant	UBE2Q2	GRCh38.p7	15:75898565	GTATATTGTTAACTA[C/T]AGTCACCATGTTGTA	92912
rs1562403	snp	A/G	0.170733	0.237101	intron-variant	UBE2Q2	GRCh38.p7	15:75864468	ctcagcaatattgac[A/G]tattgggccagacaa	92912
rs1613718	snp	A/G			intron-variant	UBE2Q2	GRCh38.p7	15:75865825	TTTTTTTTTAACCTA[A/G]AAAGGGTTTAAAGGG	92912
rs1618530	snp	G/T			intron-variant	UBE2Q2	GRCh38.p7	15:75848148	GCAAGAGAGCATATA[G/T]AGGAAAGCTCTTTGG	92912
rs1621882	snp	A/T	0	0	intron-variant	UBE2Q2	GRCh38.p7	15:75855743	TTGATTCTTAGGTAT[A/T]TAATTTTTGTTGAAA	92912
rs1665763	snp	A/C	0	0	upstream-variant-2KB	UBE2Q2	GRCh38.p7	15:75842647	CACACCCCCATGGAG[A/C]TAGGGCTGCCCACTA	92912
rs1665764	snp	A/C	0	0	intron-variant	UBE2Q2	GRCh38.p7	15:75872878	TTAAAATGAAAAACA[A/C]TACAAAAAAGAATAG	92912
rs1665765	snp	G/T	0	0	intron-variant	UBE2Q2	GRCh38.p7	15:75879816	TCCAtaaataagtgt[G/T]tctcagatttctttt	92912
rs1665770	snp	A/G			intron-variant	UBE2Q2	GRCh38.p7	15:75865522	taagtatgtgcccca[A/G]agaaatgctggcaca	92912
rs1665771	snp	A/G	0	0	intron-variant	UBE2Q2	GRCh38.p7	15:75865520	AGTATGTGCCCCAGA[A/G]AAATGCTGGCACAGG	92912
rs1695378	snp	C/T	0.324382	0.238678	intron-variant	UBE2Q2	GRCh38.p7	15:75888205	GTTTCTTTTTGAAGT[C/T]ATGAAAATGTTCTGA	92912
rs1699269	snp	A/C			intron-variant	UBE2Q2	GRCh38.p7	15:75848100	TCTATAGTACACAGA[A/C]ACACAGTAAAAGAAG	92912
rs1699270	snp	A/C	0	0	intron-variant	UBE2Q2	GRCh38.p7	15:75848015	TAGATTCACAGCTCC[A/C]ACATTTTTAAAATTT	92912
rs1699271	snp	A/T			intron-variant	UBE2Q2	GRCh38.p7	15:75879809	ataagtgtttctcag[A/T]tttcttttcattttt	92912
rs1699272	snp	C/T	0	0	intron-variant	UBE2Q2	GRCh38.p7	15:75865557	CATGAGGATCAATTT[C/T]TTCTTTTACTCAAGA	92912
rs1699273	snp	A/C/T			intron-variant	UBE2Q2	GRCh38.p7	15:75865560	GAGGATCAATTTTTT[A/C/T]TTTTACTCAAGAGTT	92912
rs1699274	snp	C/T	0	0	intron-variant	UBE2Q2	GRCh38.p7	15:75865578	TTACTCAAGAGTTAT[C/T]TAGGAAAAAAAAAAC	92912
rs1699276	snp	C/T	0.031825	0.122064	intron-variant	UBE2Q2	GRCh38.p7	15:75888334	TTTTATATGATTCTA[C/T]TTATATGAAATGTCC	92912
rs1699277	snp	G/T	0.0391387	0.134304	intron-variant	UBE2Q2	GRCh38.p7	15:75888057	AAATGTTTGGCTATG[G/T]CAAGAAATAAAGAAG	92912
rs1699278	snp	C/T	0.029116	0.117091	intron-variant	UBE2Q2	GRCh38.p7	15:75887641	TGTCACTCCCCTGTT[C/T]CTCAACCAGTTATAC	92912
rs1699279	snp	C/T	0	0	intron-variant	UBE2Q2	GRCh38.p7	15:75881809	CCAAAAAGTGACTTC[C/T]TTAAAAATATAGCAA	92912
rs1799634	snp	A/C			intron-variant	UBE2Q2	GRCh38.p7	15:75848031	ACTTCTCACTTCCTC[A/C]TAGATTCACAGCTCC	92912
rs1868020	snp	C/T	0.0678174	0.1712	intron-variant	UBE2Q2	GRCh38.p7	15:75883487	TAGTGAGATCTCGTC[C/T]CTATAAAAAAAAATT	92912
rs1910510	snp	G/T	0.13446	0.221699	intron-variant	UBE2Q2	GRCh38.p7	15:75896767	TTATAAAAATGAACT[G/T]TGAGGCTTGTTGAGT	92912
rs1910511	snp	A/G	0.0471551	0.14613	intron-variant	UBE2Q2	GRCh38.p7	15:75882640	AACAACAGTTATTAT[A/G]ATCTACTTTCAAATA	92912
rs1964677	snp	A/C	0.029116	0.117091	intron-variant	UBE2Q2	GRCh38.p7	15:75885719	GATCAACTTTGTAAC[A/C]ACCTGTCAAAAGGAA	92912
rs1968623	snp	A/G	0.029116	0.117091	intron-variant	UBE2Q2	GRCh38.p7	15:75871821	TTCCTATCAATAATt[A/G]tggggaaaagcaaga	92912
rs1976748	snp	A/G	0.499908	0.00678851	intron-variant	UBE2Q2	GRCh38.p7	15:75868610	TATTTTAAATAAGCC[A/G]TTGATCTTATGCATA	92912
rs2028949	snp	A/C	0.029116	0.117091	intron-variant	UBE2Q2	GRCh38.p7	15:75858725	CGGACACAGACCTAG[A/C]CACTCTGGCCTCTGG	92912
rs2028950	snp	A/G	0.0205511	0.0992634	intron-variant	UBE2Q2	GRCh38.p7	15:75858518	AGTAAGAGACATTCA[A/G]AAGGACAGGTCTTAG	92912
rs2047866	snp	A/G	0.478396	0.101662	upstream-variant-2KB, intron-variant	UBE2Q2	GRCh38.p7	15:75843853	GGGCCGCGGCCGGGC[A/G]CCTCACCGTGATGTT	92912
rs2047867	snp	C/T	0.029116	0.117091	intron-variant	UBE2Q2	GRCh38.p7	15:75886388	ctcatgccataatcc[C/T]agcactttgggaggc	92912
rs2121556	snp	A/C	0.121828	0.214644	intron-variant	UBE2Q2	GRCh38.p7	15:75854622	TTGAAGGAAAAAAAA[A/C]AAACAAACTAGTCTT	92912
rs2134736	snp	C/T			utr-variant-5-prime, intron-variant	UBE2Q2	GRCh38.p7	15:75844124	GGGCCGCCGCGGACT[C/T]CCCCCTCGGGGCTAG	92912
rs2307792	in-del	-/TTC	0	0	utr-variant-3-prime, nc-transcript-variant	UBE2Q2	GRCh38.p7	15:75900574	AATGTGCTTCTGGAT[-/TTC]TTGTTAAAAGTGCTT	92912
rs2441928	snp	G/T	0.170408	0.236992	intron-variant	UBE2Q2	GRCh38.p7	15:75858828	TGGAGCTTGGTTTCC[G/T]TTTAAGCATGAAGAT	92912
rs2441929	snp	A/G	0.324382	0.238678	intron-variant	UBE2Q2	GRCh38.p7	15:75880779	GCTGGGATTACAGGC[A/G]TGATTTAATATGGAT	92912
rs2441930	snp	A/G	0.317692	0.240661	intron-variant	UBE2Q2	GRCh38.p7	15:75881190	TCTTTTTAAAAAATT[A/G]AATTATATGTCCTTA	92912
rs2441931	snp	A/G	0.0584853	0.160693	intron-variant	UBE2Q2	GRCh38.p7	15:75881260	TTTATCCGTCCCTGT[A/G]GCCCCCTGTGTGCCC	92912
rs2441932	snp	A/G	0.0678174	0.1712	intron-variant	UBE2Q2	GRCh38.p7	15:75881439	AATGGCTGAATTTCT[A/G]TTGGATTTGTGTTTC	92912
rs2455896	snp	C/G	0.0739622	0.178423	intron-variant	UBE2Q2	GRCh38.p7	15:75882838	CCCAACCTAAGGAGC[C/G]GGAGACTTAGCAGGG	92912
rs2455899	snp	C/T	0.323908	0.238825	intron-variant	UBE2Q2	GRCh38.p7	15:75879466	ACCCATCTTGTCCCA[C/T]ATAGCTGTAAACCAC	92912
rs2455900	snp	C/T	0.0205511	0.0992634	intron-variant	UBE2Q2	GRCh38.p7	15:75874388	GGTGAGGCAGGAGAA[C/T]TGCTTGAACCTGGGA	92912
rs2455901	snp	C/G	0.029116	0.117091	intron-variant	UBE2Q2	GRCh38.p7	15:75863976	ATATTCAGTGAAAAA[C/G]ACAAGCTGCAGATGT	92912
rs2460798	snp	A/G	0.326976	0.237854	intron-variant	UBE2Q2	GRCh38.p7	15:75883787	TTACCTATCAACAAC[A/G]TAATGCTTTACAACT	92912
rs2460799	snp	C/T	0.0973687	0.197999	intron-variant	UBE2Q2	GRCh38.p7	15:75880563	agtgagccaagattg[C/T]gccaccacacgccag	92912
rs2460800	snp	G/T	0.324382	0.238678	intron-variant	UBE2Q2	GRCh38.p7	15:75872610	GTTTGAGGCTGCAGT[G/T]AGCTATGATCATGCT	92912
rs2460801	snp	C/T	0.170084	0.236883	intron-variant	UBE2Q2	GRCh38.p7	15:75872007	CCTACATGTTTTCCT[C/T]ACAATTCTCACAAAT	92912
rs2460803	snp	C/T			intron-variant	UBE2Q2	GRCh38.p7	15:75851398	gtgaaccactatttt[C/T]taaatgaccaatgca	92912
rs2593274	snp	A/G	0.0287284	0.116357			GRCh38.p7	15:75851892	TTCTTTTTATTTTTG[A/G]GACAGGGCCTTGTTC	92912
rs2593275	snp	A/G	0.17138	0.237316			GRCh38.p7	15:75852640	TTCTTTAGCCTAAGG[A/G]AAAAGAAACCTAAAA	92912
rs2593276	snp	C/T	0.0209421	0.100162			GRCh38.p7	15:75853267	ACGAGATCAGGAGTT[C/T]AAGACCAGCCTGGCC	92912
rs2593277	snp	A/G	0.32627	0.238082			GRCh38.p7	15:75853284	AGACCAGCCTGGCCA[A/G]CATGGTGAAACCCCG	92912
rs2593278	snp	C/T	0.325799	0.238232			GRCh38.p7	15:75855256	AGCACTTTAGGAAGC[C/T]GAGGCGGGCGGATCA	92912
rs2593279	snp	A/C	0.0287284	0.116357			GRCh38.p7	15:75855272	GAGGCGGGCGGATCA[A/C]TTGAGGCCAGGAGTT	92912
rs2593280	snp	A/G	0.326035	0.238157			GRCh38.p7	15:75858624	TGAAATTCGTGGAGA[A/G]TGTACTACCCTGTCT	92912
rs2593281	snp	A/G	0.170408	0.236992			GRCh38.p7	15:75860847	CTTGGATCCCATGCC[A/G]TCTTTCTTGGCTGAC	92912
rs2593282	snp	C/G	0.0232847	0.105357			GRCh38.p7	15:75863227	GCTGTCAATATCCCC[C/G]TAACCTCCACCTTTG	92912
rs2593299	snp	C/G	0.113334	0.209338			GRCh38.p7	15:75844766	ACTGCAGAATATTCT[C/G]TTGGTTATAATAGGC	92912
rs2593300	snp	C/T	0.0209421	0.100162			GRCh38.p7	15:75847193	TAAATGCTTCATAAA[C/T]ATTTGAGTATATAGC	92912
rs2593301	snp	C/T	0.029116	0.117091			GRCh38.p7	15:75849086	AAGTGTTAGAATTTT[C/T]ACTCTGCTTTTGTGG	92912
rs2593302	snp	A/C	0.170408	0.236992			GRCh38.p7	15:75849339	TATCTCTGAACCTTC[A/C]AGAAGTTTGTGCATC	92912
rs2604403	snp	C/G	0.170084	0.236883			GRCh38.p7	15:75861341	CTGAAACTCAGAATG[C/G]CATGAGGCTTCACCA	92912
rs2604405	snp	A/G	0.170084	0.236883			GRCh38.p7	15:75869788	ATGTCTTTGGAATGC[A/G]CTCTACTAAATTtgc	92912
rs2604406	snp	C/G	0.0678174	0.1712			GRCh38.p7	15:75867782	TGAAAGAGCATTTTC[C/G]AAATGCCAATTTCAA	92912
rs2604409	snp	A/T	0.0310518	0.120672			GRCh38.p7	15:75867166	TCCACCTCTTCCTTT[A/T]AGCTCAGGAGCTGGA	92912
rs2655126	snp	C/T	0.170733	0.237101	intron-variant	UBE2Q2	GRCh38.p7	15:75856169	GACGGGGTCTCACTC[C/T]GTCACCTAGGCTAGA	92912
rs2655137	snp	A/C	0.171057	0.237209	intron-variant	UBE2Q2	GRCh38.p7	15:75869557	aggtcctcagacacc[A/C]aatgttggtatcttg	92912
rs2655138	snp	C/G	0.0209421	0.100162	intron-variant	UBE2Q2	GRCh38.p7	15:75862642	TTTTTGTAAAGATGG[C/G]GTCTCAATATGTTGC	92912
rs2675219	snp	C/T	0	0	intron-variant	UBE2Q2	GRCh38.p7	15:75856247	acacacacacacaca[C/T]gtatatacacatata	92912
rs3040996	in-del	-/GAAAA	0.0287284	0.116357	intron-variant	UBE2Q2	GRCh38.p7	15:75864790	GCAAAAAATGAAAAA[-/GAAAA]CACTAGATTTAAAAA	92912

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