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
rs3931	snp	C/T	0.395298	0.203442	synonymous-codon, downstream-variant-500B, nc-transcript-variant	NOSTRIN, SPC25	GRCh38.p7	2:168864871	AGATCCAAACCACCA[C/T]CCTCCTTCTTTTTTC	115677
rs10181	snp	A/C/T	1.65718e-05	0.00287848	synonymous-codon, downstream-variant-500B, nc-transcript-variant	NOSTRIN, SPC25	GRCh38.p7	2:168864937	GTTGCCAGCATTTGA[A/C/T]GGTAACTCCTCCACA	115677
rs471087	snp	G/T	0.41023	0.191902	intron-variant, upstream-variant-2KB	NOSTRIN	GRCh38.p7	2:168845128	TTGAACATAAGCTCC[G/T]GGTACTCTCTTGGTT	115677
rs472233	snp	C/T	0.433818	0.169443	intron-variant	NOSTRIN	GRCh38.p7	2:168832237	AGATCGTAATTCCTC[C/T]TAGAATGTATTCCCT	115677
rs474538	snp	A/G	0.440057	0.162414	intron-variant	NOSTRIN	GRCh38.p7	2:168838686	CTATCTATTCCCCAT[A/G]TACAAGCCAAGCTGA	115677
rs474751	snp	A/G	0.436408	0.16659	intron-variant, upstream-variant-2KB	NOSTRIN	GRCh38.p7	2:168845527	GGGAAGGCTATGATT[A/G]TCTTCATTATCAGAA	115677
rs475808	snp	C/G	0.382473	0.212016	intron-variant	NOSTRIN	GRCh38.p7	2:168819056	GGAAAGAAAAAAATG[C/G]AAAAGGGCTAGAGAA	115677
rs479661	snp	C/T	0.16846	0.236329	missense, downstream-variant-500B, nc-transcript-variant	NOSTRIN, SPC25	GRCh38.p7	2:168864867	CCAAACCACCATCCT[C/T]CTTCTTTTTTCTCGT	115677
rs481067	snp	A/C	0.495818	0.0455352	intron-variant	NOSTRIN	GRCh38.p7	2:168835859	ATTTTGTTCCTGTAC[A/C]CCAATATTATTCGTG	115677
rs482435	snp	A/G	0.391024	0.206427	intron-variant	NOSTRIN	GRCh38.p7	2:168819535	GTTGAGATAAAAGCC[A/G]TTCAGCGCTAGAGGC	115677
rs486153	snp	A/G	0.471958	0.115042	intron-variant	NOSTRIN	GRCh38.p7	2:168826456	AGGAAGCAAGGGAGG[A/G]AGGGAGGGAAGAGAA	115677
rs486838	snp	A/G	0.368529	0.220116	intron-variant	NOSTRIN	GRCh38.p7	2:168826446	GGAGGAAGGGAGGGA[A/G]GAGAAAGAAAGGAAA	115677
rs487756	snp	C/T	0.391024	0.206427	intron-variant	NOSTRIN	GRCh38.p7	2:168830049	CTCTATTCAGAGTTT[C/T]GGGTGATGGACAGAA	115677
rs488621	snp	A/G	0.500003	0.00218935	intron-variant	NOSTRIN	GRCh38.p7	2:168851042	TGACTTCCATTTTGC[A/G]TAACAACTGGCTGAT	115677
rs490278	snp	A/G	0.478603	0.101197	intron-variant	NOSTRIN	GRCh38.p7	2:168814693	CATAATTCAAGATAC[A/G]GTGAAGGAGGACATG	115677
rs494120	snp	A/G	0.095934	0.196885	intron-variant	NOSTRIN	GRCh38.p7	2:168814219	TGACCTCAGAATCAC[A/G]TCACTGTGTGGGAGA	115677
rs495074	snp	C/T	0.49962	0.0137727	intron-variant	NOSTRIN	GRCh38.p7	2:168830831	TGCTGCATGGATTGA[C/T]GTGGAAGATGATGTG	115677
rs495135	snp	A/G	0.453087	0.145793	intron-variant	NOSTRIN	GRCh38.p7	2:168830849	GGAAGATGATGTGAT[A/G]GGACTAGCAACAATA	115677
rs497808	snp	A/C	0.479014	0.100263	intron-variant	NOSTRIN	GRCh38.p7	2:168848527	CACTGCTTGCAAATG[A/C]AAGTAGTAAAAGGCT	115677
rs498231	snp	A/G	0.49975	0.0111793	intron-variant	NOSTRIN	GRCh38.p7	2:168810985	GTTATAAATTTATTA[A/G]TTACCCTTTATAAAT	115677
rs498488	snp	C/T	0.0955749	0.196603	intron-variant	NOSTRIN	GRCh38.p7	2:168820374	ttacaacgtgccagg[C/T]gtcattctgggtgtt	115677
rs501303	snp	C/T	0.411242	0.191052	intron-variant	NOSTRIN	GRCh38.p7	2:168840918	GAATTCTGGAATTTG[C/T]AATTTTTACAAGCAT	115677
rs503664	snp	C/G	0.479014	0.100263	intron-variant	NOSTRIN	GRCh38.p7	2:168833166	CTATAATAATTTTCT[C/G]CCCAGTTACAATTCA	115677
rs505283	snp	A/G	0.496714	0.0404017	intron-variant, upstream-variant-2KB	NOSTRIN	GRCh38.p7	2:168846524	TAAGTAATGAAACCA[A/G]TTCCACAAACCACAT	115677
rs506362	snp	G/T	0.470521	0.117772	intron-variant	NOSTRIN	GRCh38.p7	2:168864530	tgggaggccaaggtg[G/T]gtggatcacaaggtc	115677
rs508423	snp	C/T	0.410399	0.191761	intron-variant	NOSTRIN	GRCh38.p7	2:168844544	TTCCAGCCTCAATGT[C/T]CTCATAATGTCATGA	115677
rs511013	snp	C/T	0.285257	0.247501	intron-variant	NOSTRIN	GRCh38.p7	2:168827417	CCTGTTCATGTCCTG[C/T]TGCTGCTCTTGGGGT	115677
rs514629	snp	C/T	0.258288	0.249863	intron-variant	NOSTRIN	GRCh38.p7	2:168808611	CACAGTATTAAGCTA[C/T]GGATTTTTATGTATT	115677
rs518337	snp	A/G	0.499653	0.0131743	intron-variant	NOSTRIN	GRCh38.p7	2:168842840	TTTTTTTCTTATAAA[A/G]ATCTTTCATTTTGTC	115677
rs519345	snp	A/G	0	0	intron-variant	NOSTRIN	GRCh38.p7	2:168860346	ACACAGTAGGGCTTA[A/G]AAATCTTTGAATTAT	115677
rs519599	snp	C/T	0.15698	0.23205	intron-variant	NOSTRIN	GRCh38.p7	2:168831170	CACACAGCTAATGTG[C/T]GGGTGCCTTGCTCTT	115677
rs522893	snp	A/G	0.489689	0.0710578	intron-variant	NOSTRIN	GRCh38.p7	2:168834219	TTCTTGGCCTAGAGT[A/G]AAAAACATACAAACA	115677
rs526418	snp	A/G	0.496245	0.0431677	intron-variant	NOSTRIN	GRCh38.p7	2:168838603	ATCCTCTCTCAGGCC[A/G]CAATCATCTTTTGCT	115677
rs527393	snp	A/G	0.497151	0.037632	intron-variant	NOSTRIN	GRCh38.p7	2:168853247	GCAAAGCACCCCAAT[A/G]TCTGACTTTATAGTC	115677
rs529002	snp	A/C	0.404035	0.196909	intron-variant	NOSTRIN	GRCh38.p7	2:168847386	AGGTCTAGGGAGGTG[A/C]TCAGGAATCTGACTT	115677
rs531328	snp	G/T	0.4862	0.0819127	intron-variant	NOSTRIN	GRCh38.p7	2:168844328	TCTCCAGAATTGATA[G/T]TTATTTAATTTGGTC	115677
rs531864	snp	C/T	0.491104	0.0660973	intron-variant	NOSTRIN	GRCh38.p7	2:168847150	TAATGGCACGGGAAA[C/T]TGTTCACATGTACGG	115677
rs532779	snp	A/T	0.483272	0.0899109	intron-variant	NOSTRIN	GRCh38.p7	2:168847241	TCATACATATACACA[A/T]ACCTAGACTGAAATA	115677
rs533492	snp	A/G	0.158962	0.232835	intron-variant	NOSTRIN	GRCh38.p7	2:168863296	TTAGAGACCGAGAAT[A/G]ATGTCCTTTAAGAAT	115677
rs534310	snp	C/T	0.261884	0.249717	intron-variant	NOSTRIN	GRCh38.p7	2:168863363	AAAGGAGTTAATAAT[C/T]TCCTTTGTCTTAGAA	115677
rs534771	snp	A/C	0.27278	0.24896	intron-variant, utr-variant-3-prime	NOSTRIN	GRCh38.p7	2:168863705	ATGTCTCTGCATTAT[A/C]CCTGATTTCACAGGC	115677
rs539400	snp	C/G	0.270351	0.24917	intron-variant	NOSTRIN	GRCh38.p7	2:168863193	GCCAGCTTCCCTAAG[C/G]CTCCAACGTCGTGTT	115677
rs540652	snp	C/T	0.499437	0.016763	intron-variant, missense, nc-transcript-variant	NOSTRIN	GRCh38.p7	2:168850918	TAAGATACCAAGACA[C/T]ATTCCTTCCTGGAAA	115677
rs543262	snp	C/T	0.460702	0.134554	intron-variant	NOSTRIN	GRCh38.p7	2:168807717	TACCTCGCTCCCAGC[C/T]ATACTCTGCCAATTC	115677
rs546146	snp	C/G	0.494855	0.0504572	intron-variant	NOSTRIN	GRCh38.p7	2:168852687	GATCAGGCAACAAGA[C/G]GGTAGAAGGCAGAGG	115677
rs548367	snp	C/T	0.489318	0.0722982	intron-variant	NOSTRIN	GRCh38.p7	2:168812952	AAGTCTGTTTCAGCT[C/T]GCTCATATCTTTCTT	115677
rs549582	snp	A/G	0.136847	0.222927	intron-variant	NOSTRIN	GRCh38.p7	2:168833579	TTTCCTAGTCTACAT[A/G]GTTGAATTTAACTGA	115677
rs550081	snp	A/G	0.385359	0.210185	intron-variant	NOSTRIN	GRCh38.p7	2:168822171	GTCAATAAATATCTC[A/G]TCGCACTTAAAAATA	115677
rs551037	snp	A/G	0.100231	0.200173	intron-variant	NOSTRIN	GRCh38.p7	2:168813198	GGCTTTCTAATCTGG[A/G]TAATGAGTTGAATTC	115677
rs552445	snp	C/G	0.434687	0.168495	intron-variant	NOSTRIN	GRCh38.p7	2:168833261	GAAATGAGAGTGTGA[C/G]GCATGAATATTTGGT	115677
rs553827	snp	C/G	0.0737376	0.17729	intron-variant	NOSTRIN	GRCh38.p7	2:168846972	TACTTCCTCAAGACA[C/G]TTTTATAGAAAGGAA	115677
rs557002	snp	G/T	0.485118	0.0849685	intron-variant	NOSTRIN	GRCh38.p7	2:168825019	gtaatcccagaactt[G/T]ggaaggccaaggcag	115677
rs558922	snp	C/T	0.495521	0.0471118	intron-variant	NOSTRIN	GRCh38.p7	2:168825239	TGTAAACAGGGATAA[C/T]AAGACCTCTCAAGGG	115677
rs559113	snp	A/T	0.499891	0.00738737	intron-variant, upstream-variant-2KB	NOSTRIN	GRCh38.p7	2:168846419	CTCTGAAGGAATTTG[A/T]ACATCCAACCTGTAG	115677
rs560952	snp	A/G	0.479744	0.0985793	intron-variant	NOSTRIN	GRCh38.p7	2:168847977	TTTGACAAGTGCTGA[A/G]CCACTAGCATCAATC	115677
rs566465	snp	A/T	0.499609	0.0139722	intron-variant	NOSTRIN	GRCh38.p7	2:168848594	TATGCATACCATGGA[A/T]TATTATTCAGCCAAA	115677
rs569821	snp	A/T	0	0	intron-variant	NOSTRIN	GRCh38.p7	2:168812295	TCTCTTTAGAGTTGC[A/T]TATTACGGAGCTATC	115677
rs569997	snp	C/T	0.498673	0.0257246	intron-variant	NOSTRIN	GRCh38.p7	2:168858383	CTGGTAGATTTTGTG[C/T]CACCCACGGAAGGTT	115677
rs572411	snp	A/G	0.155656	0.231515	intron-variant	NOSTRIN	GRCh38.p7	2:168829520	AAGCCTGACCAACAT[A/G]GCGATCCCTGGTCTC	115677
rs576062	snp	C/T	0.498693	0.0255257	intron-variant	NOSTRIN	GRCh38.p7	2:168859176	GTTGATTGTAGAAGG[C/T]AGATTTTTGGTGGTC	115677
rs577192	snp	C/T	0.162253	0.234095	intron-variant	NOSTRIN	GRCh38.p7	2:168852594	GGTGTCACTCTTCTC[C/T]GATATGGAGAACAAG	115677
rs578521	snp	C/T	0.40595	0.195396	intron-variant	NOSTRIN	GRCh38.p7	2:168837951	cctgatctttatata[C/T]tgcagtttctgaaga	115677
rs578797	snp	A/C	0.410399	0.191761	intron-variant	NOSTRIN	GRCh38.p7	2:168844845	ACTGCACACTAGCCT[A/C]GGCGACAGAGCAAGA	115677
rs580507	snp	A/G	0.322959	0.239117	intron-variant	NOSTRIN	GRCh38.p7	2:168862392	TGTTTCCAAGTTCAA[A/G]TCTTGTGTTGCCACA	115677
rs581363	snp	C/T	0.270351	0.24917	intron-variant	NOSTRIN	GRCh38.p7	2:168862471	AAAAGGTGGGGTACA[C/T]CTCTAATCACTTTCC	115677
rs696805	snp	C/T	0.00199481	0.0315187	intron-variant	NOSTRIN	GRCh38.p7	2:168816123	CTGCCTCCATTCATC[C/T]CACTCAGCCATGTGC	115677
rs700547	snp	C/T	0.0611083	0.163768	upstream-variant-2KB, intron-variant	NOSTRIN	GRCh38.p7	2:168801721	TGGCCTATTGATGTA[C/T]GACAGCCATTTGCTA	115677
rs700548	snp	C/T	0.0633504	0.166319	intron-variant	NOSTRIN	GRCh38.p7	2:168827947	TGCTTTTTTCCCAGT[C/T]ATTTTTCATTTAGAT	115677
rs829950	snp	C/T	0.49962	0.0137727	intron-variant	NOSTRIN	GRCh38.p7	2:168797545	GTCCTTATAGCTTTA[C/T]GTTGGCCCAGCTGAC	115677
rs829951	snp	C/T	0.00716266	0.059414	intron-variant	NOSTRIN	GRCh38.p7	2:168790908	AGGATTTTTTTCCTT[C/T]TGTCCTgaataagtt	115677
rs829952	snp	C/G	0.0315505	0.12225	intron-variant, upstream-variant-2KB	NOSTRIN, CERS6-AS1	GRCh38.p7	2:168786845	agctactctggagga[C/G]gggggaggcagggaa	115677
rs829955	snp	C/T	0.177503	0.239258	intron-variant	NOSTRIN	GRCh38.p7	2:168805514	ATACTTTCTTATGAT[C/T]GGATTCTTTCCCTTA	115677
rs829956	snp	G/T	0.00676609	0.0577691	intron-variant	NOSTRIN	GRCh38.p7	2:168804951	CATTTTGAAGTCAGG[G/T]TGAATGTAAATATTT	115677
rs829957	snp	A/C	0.252702	0.249985	upstream-variant-2KB, intron-variant	NOSTRIN	GRCh38.p7	2:168802324	ATGTCTCCAACAATT[A/C]TTGCGCTTGGTCTGA	115677
rs829958	snp	C/T	0.230017	0.2492	upstream-variant-2KB, intron-variant	NOSTRIN	GRCh38.p7	2:168802273	TCTCAGCCTGCAGTA[C/T]TAATCATGCTTTTTA	115677
rs829959	snp	C/T	0.0209421	0.100162	upstream-variant-2KB, intron-variant	NOSTRIN	GRCh38.p7	2:168801338	agctactcaagaggt[C/T]gaggcagaaggattt	115677
rs829960	snp	C/T	0.102014	0.201495	intron-variant, upstream-variant-2KB	NOSTRIN	GRCh38.p7	2:168823569	ttggacataaacaga[C/T]atgtacacagagaaa	115677
rs830020	snp	C/T	0.499053	0.0217445	intron-variant	NOSTRIN	GRCh38.p7	2:168829246	gaaagaaagaaAAAC[C/T]GTTCTAGAAGGAAAG	115677
rs830021	snp	G/T	0.412082	0.190341	intron-variant	NOSTRIN	GRCh38.p7	2:168828762	TTCTATTGCTTGAAT[G/T]TATCACAATTTATTT	115677
rs830022	snp	C/T	0.0566069	0.158427	intron-variant, upstream-variant-2KB	NOSTRIN	GRCh38.p7	2:168823174	aaaaaattagccagg[C/T]gtggtggctcacgcc	115677
rs830023	snp	A/G	0.00676609	0.0577691	intron-variant	NOSTRIN	GRCh38.p7	2:168820011	GCTCCTGGAGGCTGA[A/G]TAGCTGGAGTCCCAA	115677
rs830024	snp	C/G	0.339341	0.233491	intron-variant	NOSTRIN	GRCh38.p7	2:168818254	AGGCGAGAGGAGTTC[C/G]CGAGCACAGGAGTCT	115677
rs830025	snp	A/T	0.172834	0.237793	intron-variant	NOSTRIN	GRCh38.p7	2:168818153	AAAAACATAAAATAA[A/T]AAAATAGAGCTAAGC	115677
rs830026	snp	A/G	0.188501	0.242318	intron-variant	NOSTRIN	GRCh38.p7	2:168818145	AAAATAATAAAATAG[A/G]GCTAAGCCCTTCTCA	115677
rs830027	snp	C/T	0.443866	0.157848	intron-variant	NOSTRIN	GRCh38.p7	2:168817869	AAAGACATTTTCATA[C/T]TGAAGCTCTGTCATT	115677
rs830028	snp	A/G	0.444533	0.157025	intron-variant	NOSTRIN	GRCh38.p7	2:168817672	AGGGAAAACGTAAGC[A/G]ATGGCAGCTCTAGAA	115677
rs830029	snp	C/T	0.450734	0.149016	intron-variant	NOSTRIN	GRCh38.p7	2:168817498	AATTTTATGCAGAAT[C/T]CCACTGTATCATATA	115677
rs830030	snp	A/T	0.4973	0.0366419	intron-variant	NOSTRIN	GRCh38.p7	2:168817357	CAAACCCCTTGAGCT[A/T]TAAGGTTTGAAAGCC	115677
rs830031	snp	A/G	0.399968	0.200024	intron-variant	NOSTRIN	GRCh38.p7	2:168812521	atgggtatagcatgt[A/G]ttaataagtttctgc	115677
rs830194	snp	A/G	0.442113	0.159977	intron-variant	NOSTRIN	GRCh38.p7	2:168836132	GTGAAGACTGACATG[A/G]AAAGAAATAAGAGTC	115677
rs853666	snp	A/G	0.446641	0.154377	intron-variant	NOSTRIN	GRCh38.p7	2:168817632	CTAAAGTGTGCATTC[A/G]TTCCTAAGCTTAGTG	115677
rs862637	snp	C/T	0	0	intron-variant	NOSTRIN	GRCh38.p7	2:168824761	aaacaaacaaacaaa[C/T]aaaaaaaGGGTTGAT	115677
rs862638	snp	C/T	0.450609	0.149185	intron-variant	NOSTRIN	GRCh38.p7	2:168817383	CTGAGGTAGCCCCTG[C/T]GGGCTCCCCACAAAC	115677
rs865520	snp	A/G			intron-variant	NOSTRIN	GRCh38.p7	2:168849540	tttgtatttttagta[A/G]agacggggttttgcc	115677
rs1402835	snp	C/T	0	0	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	NOSTRIN	GRCh38.p7	2:168834268	TACAAGCTGGAAAAG[C/T]GCTTCATGTTTCTTG	115677
rs1568550	snp	A/G	0.331411	0.236373	intron-variant	NOSTRIN	GRCh38.p7	2:168821687	CAACAGGAGCTGCTC[A/G]AACATCACTGCCTCA	115677
rs2010230	snp	A/C	0.163236	0.234461	upstream-variant-2KB, intron-variant	NOSTRIN	GRCh38.p7	2:168801041	AAAAGAAATTTAGGT[A/C]Aggcacagtggcaca	115677
rs2010235	snp	G/T	0.384401	0.210799	upstream-variant-2KB, intron-variant	NOSTRIN	GRCh38.p7	2:168800921	cccatctcttttttt[G/T]ttttttttttaaaag	115677
rs2140046	snp	C/T	0.474182	0.110646	intron-variant	NOSTRIN	GRCh38.p7	2:168849569	CCACGTTGGGCAGGC[C/T]GGCCTTGAACTCCTG	115677
rs2177076	snp	A/C	0.427119	0.176434	intron-variant	NOSTRIN	GRCh38.p7	2:168841869	cttaggtttaacaaa[A/C]tacggacatccatgt	115677

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