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
rs491973	snp	C/T	0.499393	0.0174067	upstream-variant-2KB, missense	SART1, TSGA10IP	GRCh38.p7	11:65959830	CCATTCTCACCCCCA[C/T]TGACCTGTGGCTCCT	9092
rs493899	snp	A/C	0.494651	0.0514399	downstream-variant-500B	SART1	GRCh38.p7	11:65980481	TTCTCTCAAAAGCCT[A/C]GGAGGAGGCTGGGAA	9092
rs501353	snp	G/T	0.494896	0.0502606	intron-variant	SART1	GRCh38.p7	11:65972078	atatgaatttagggg[G/T]tacacaaTTCCTAGA	9092
rs542332	snp	A/G	0.494651	0.0514399	intron-variant	SART1	GRCh38.p7	11:65976950	CAGCCCCACCCACTG[A/G]TCACCACCTGCCAGG	9092
rs543952	snp	A/G	0.315086	0.241379	intron-variant	SART1	GRCh38.p7	11:65976804	ATCTCCAGCTTGAGC[A/G]CCCCCAAACGCCCAC	9092
rs550435	snp	A/G	0.497165	0.0375428	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65965180	GCGGGAGAAGCTGGC[A/G]GCTGCCAAGGAGAAG	9092
rs552130	snp	A/G	0.493136	0.0581782	intron-variant	SART1	GRCh38.p7	11:65965329	TTCCTGAAGAGGGGA[A/G]AAAGTGATGCTCAAG	9092
rs556643	snp	A/G	0.498774	0.0247239	intron-variant	SART1	GRCh38.p7	11:65965818	CAGGGGACACTGGTG[A/G]CCTTGCTACCGGAAT	9092
rs586921	snp	A/G	0.26326	0.249648	downstream-variant-500B	SART1	GRCh38.p7	11:65980230	TTCTGCACGGCTAGA[A/G]CTGCGGGGCTGAGTC	9092
rs593525	snp	A/G	0.495927	0.0449436	upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime	SART1, TSGA10IP	GRCh38.p7	11:65960328	GGCTCCCTGTGTGGC[A/G]CAACTCAGCATGTGT	9092
rs622779	snp	C/T	0.329005	0.237188	intron-variant	SART1	GRCh38.p7	11:65976776	CACCCCCCAGCGGCG[C/T]GGCCCTCACATCCTG	9092
rs642293	snp	A/G	0.49306	0.0584955	intron-variant	SART1	GRCh38.p7	11:65962746	ccaggaaaccaggag[A/G]gctataggccagggg	9092
rs649000	snp	A/G	0.486398	0.0813386	intron-variant	SART1	GRCh38.p7	11:65975462	cacaccactgcactc[A/G]aaagagtgggcaaga	9092
rs649066	snp	C/T	0	0	intron-variant	SART1	GRCh38.p7	11:65975408	aaaaaaaaaaaaaTT[C/T]TTCCAGGggccgggt	9092
rs660118	snp	C/G	0.498429	0.0279843	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967703	AGCACCTGCGGGGAC[C/G]CCGGCGGTGGAGCTC	9092
rs679581	snp	A/G	0.485049	0.0851591	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	SART1	GRCh38.p7	11:65979182	AGGTGAGACCTGGCC[A/G]TCAAATGACACAAAC	9092
rs688862	snp	A/G	0.49783	0.0328695	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65965922	AATGGCATGCTCCAC[A/G]GTGAGGCCCTGCAGG	9092
rs754532	snp	C/T	0.343701	0.231776	utr-variant-3-prime, downstream-variant-500B	SART1	GRCh38.p7	11:65979586	CTGGGTCACTGTACA[C/T]GGGACAAGTCTCCCA	9092
rs879509	snp	A/G	0.0232847	0.105357	utr-variant-3-prime	SART1	GRCh38.p7	11:65979723	GGTGTACGTGGGGCC[A/G]GGCACCAGTATCCTG	9092
rs948478	snp	G/T			intron-variant	SART1	GRCh38.p7	11:65977508	AGCCACAGCTCCAGG[G/T]CCGCCTGAGAAGGCA	9092
rs1144796	snp	C/T	0.00501711	0.0498336	intron-variant	SART1	GRCh38.p7	11:65966072	TGCTCTGTGCTGCCC[C/T]CAGGCGTGCTGCAGG	9092
rs1151505	snp	C/T	0.494774	0.0508504	intron-variant	SART1	GRCh38.p7	11:65967068	AAGGTACTTAACCTC[C/T]CTGTGCCCCAGTTTC	9092
rs1151506	snp	G/T			intron-variant	SART1	GRCh38.p7	11:65975393	TCCCGGGGggccggg[G/T]ggttgccccctttta	9092
rs1151508	snp	A/G	0.0134861	0.0810011	intron-variant	SART1	GRCh38.p7	11:65976308	GGGTCCTCCCTGGCA[A/G]CAGCCAGACAGGCCA	9092
rs1192168	snp	G/T	0.495745	0.0459295	intron-variant	SART1	GRCh38.p7	11:65963474	AGGAAAGGAAGAGtt[G/T]tttttttgttttgtt	9092
rs1204011	snp	C/T	0.26326	0.249648	intron-variant	SART1	GRCh38.p7	11:65973615	GGTGGGCCCCGGGCA[C/T]GCACACATTCCCTCT	9092
rs1211380	snp	C/T	0.128288	0.218372	intron-variant	SART1	GRCh38.p7	11:65972863	TTCTATGTAGTTACA[C/T]GTTCACTTTTTTCTT	9092
rs1211729	snp	G/T	0.496999	0.0386216	intron-variant	SART1	GRCh38.p7	11:65974392	cacccggctGATATG[G/T]ttttttttttttttt	9092
rs1212282	snp	G/T	0	0	intron-variant	SART1	GRCh38.p7	11:65963694	agaagttcaagacca[G/T]cctggccaagatggt	9092
rs1786169	snp	A/C			intron-variant	SART1	GRCh38.p7	11:65973028	aatacaaaaaaatta[A/C]ccagacgtggtggcg	9092
rs2276015	snp	A/G	0.0879971	0.190408	intron-variant	SART1	GRCh38.p7	11:65976832	GAGGCTCTGGACACC[A/G]AGCCCGGTGCTCATC	9092
rs2276016	snp	A/G	0.289399	0.246876	intron-variant	SART1	GRCh38.p7	11:65976794	TGAGCACCCCCAAAC[A/G]CCCACCCCCCAGCGG	9092
rs2508192	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65963654	GCCTGGCTAATTTTT[A/G]TATTTTTAGTAGAGA	9092
rs2509757	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65963530	tccattgcccaggct[A/G]gagtgcagtggcgca	9092
rs2845569	snp	A/G			upstream-variant-2KB, downstream-variant-500B	SART1, TSGA10IP	GRCh38.p7	11:65960811	TCAGTGTATCCCTGG[A/G]ACCCCTGGAATTGAA	9092
rs2845575	snp	A/C			intron-variant	SART1	GRCh38.p7	11:65970824	CCCACCATCCCCCTC[A/C]TCAGCTCATGAATCC	9092
rs2845576	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65970777	CAGCAGCTCATGAAT[C/T]CCACCATCCCCCTCC	9092
rs2845581	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65963543	AGTGAGCTGAGATCG[C/T]GCCACTGCACTCTAG	9092
rs2847724	snp	A/C			intron-variant	SART1	GRCh38.p7	11:65963585	ctcctgggttcaagc[A/C]attctcctacctcag	9092
rs2847725	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65963608	tacctcagcctcccg[A/G]gtatctgggattaca	9092
rs3016188	snp	G/T			intron-variant	SART1	GRCh38.p7	11:65963582	aggtaggagaatggc[G/T]tgaacccaggaggca	9092
rs4930331	snp	C/T	0.0441095	0.141807	intron-variant	SART1	GRCh38.p7	11:65967074	CTTAACCTCCCTGTG[C/T]CCCAGTTTCCCTAGC	9092
rs5792377	in-del	-/AAAAAC/AAAAC	0.642672	0.0904971	upstream-variant-2KB	SART1	GRCh38.p7	11:65961205	CCTATCTCAAGGGAA[-/AAAAAC/AAAAC]AAAACAAAACAAAAC	9092
rs7940585	snp	C/T	0.0221141	0.102801	intron-variant	SART1	GRCh38.p7	11:65968403	CATTGGTGAACAGGA[C/T]AGCCATGGGGCCCTG	9092
rs7948137	snp	A/G	0.0103295	0.0711199	intron-variant	SART1	GRCh38.p7	11:65976049	AAACCGGAGTTTGTC[A/G]GGGGAGGGGCAGGTG	9092
rs7952056	snp	C/T	0.432939	0.170391	intron-variant	SART1	GRCh38.p7	11:65977126	TCAGGGCAGCCATGA[C/T]TTGGGTGGGCTTGGG	9092
rs9326363	snp	C/G	0.00199481	0.0315187	intron-variant	SART1	GRCh38.p7	11:65978255	GTAGGCCGCCCGACC[C/G]TCCTGCCCTACCACT	9092
rs9988860	snp	C/G	0.0221141	0.102801	intron-variant	SART1	GRCh38.p7	11:65978306	GGGGTTTGTCTCCCT[C/G]CAGCCCCAGCCCCAG	9092
rs10791834	snp	A/G	0.00755907	0.0610114	intron-variant	SART1	GRCh38.p7	11:65973131	GTGAGCCGAGATCGC[A/G]CCACTGCACTCCAGC	9092
rs10896069	snp	C/T	0.100588	0.200439	intron-variant	SART1	GRCh38.p7	11:65970667	GGTGGTGCAAAGAGA[C/T]GGGAGATGCTGTTCT	9092
rs10896070	snp	C/T	0.340108	0.233197	intron-variant	SART1	GRCh38.p7	11:65972997	AACACAGTGAAACCC[C/T]GTCTCTACTAAAAAA	9092
rs10896071	snp	C/G	0.0185938	0.0946107	intron-variant	SART1	GRCh38.p7	11:65974955	TGAGGCAGGAGAATG[C/G]TGTGAACCCAGGAGG	9092
rs11227367	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65972130	TGTCCATCTCATGTA[A/G]TTCATTTCTAGGTTA	9092
rs11227368	snp	C/T	0.490943	0.0666801	intron-variant	SART1	GRCh38.p7	11:65972899	GAACGTGGCCGGGCG[C/T]GATGGCTCACGCCTG	9092
rs11227369	snp	C/T	0.0558544	0.157504	intron-variant	SART1	GRCh38.p7	11:65978514	GGGTCAATCAACACC[C/T]GCCCTGTTATTATAC	9092
rs11227370	snp	C/T	0.356811	0.226034	downstream-variant-500B	SART1	GRCh38.p7	11:65980222	GCTGTCGCTTCTGCA[C/T]GGCTAGAGCTGCGGG	9092
rs11545221	snp	G/T	0.125087	0.216557	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65978665	GAAGACAGAGCGGCG[G/T]ATGAAGAAGCTGGAC	9092
rs11606402	snp	G/T	0.44252	0.159487	intron-variant	SART1	GRCh38.p7	11:65963482	AAGAGtttttttttt[G/T]ttttgttttgttttt	9092
rs11821955	snp	A/G	0.0372196	0.131242	intron-variant	SART1	GRCh38.p7	11:65974852	catccaggctagtac[A/G]gtgaaaccccatctc	9092
rs12288643	snp	A/T	0	0	intron-variant	SART1	GRCh38.p7	11:65978181	CACCTGCGTGAGCCC[A/T]TCACTGGCTTTCCTG	9092
rs12575514	snp	A/C	0.183568	0.241012	intron-variant	SART1	GRCh38.p7	11:65970344	CCAAAATGTCTTTTT[A/C]GTTTTTTGTTGTAAG	9092
rs12575735	snp	C/T	0.0254355	0.109867	intron-variant	SART1	GRCh38.p7	11:65977760	CTCCTCTGTCTCGGG[C/T]CAGGGCCATCGATGA	9092
rs12577625	snp	A/G	0.0876345	0.190099	intron-variant	SART1	GRCh38.p7	11:65970428	ATTCTAGAGTATGTG[A/G]GAGACACATTTATGA	9092
rs12785894	snp	G/T			intron-variant	SART1	GRCh38.p7	11:65975276	cctggttgatctttg[G/T]gttttttgtagagac	9092
rs12797319	snp	A/G	0.466618	0.124806	intron-variant	SART1	GRCh38.p7	11:65968201	GATCTGCCTGCCTCT[A/G]CCTCCGAAAATGCTA	9092
rs12806587	snp	G/T			missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965772	AGGAGTTCGGGCAGA[G/T]GCGGCAGGTGAGGCT	9092
rs12808163	snp	A/T			intron-variant	SART1	GRCh38.p7	11:65975248	gctgagactacaggc[A/T]tacaccaccatgcct	9092
rs12808809	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65975287	tttgtgttttttgta[A/G]agactgtgcttcacc	9092
rs28372938	snp	G/T	0.0898077	0.191933	upstream-variant-2KB	SART1	GRCh38.p7	11:65961528	CCGGGTTAATTCCGC[G/T]TCCCTTGAGGAGCGC	9092
rs34227638	in-del	-/C			intron-variant, utr-variant-5-prime	SART1	GRCh38.p7	11:65965080	AGCCTCACGTCTGGG[-/C]CCCCCTTCCAGAGGC	9092
rs34450536	multinucleotide-polymorphism	AG/GA			intron-variant	SART1	GRCh38.p7	11:65963545	AGAGTGCAGTGGCAC[AG/GA]TCTCAGCTCACTGCA	9092
rs34639848	in-del	-/A			intron-variant	SART1	GRCh38.p7	11:65970073	ACACACTGTGCAGGC[-/A]AAAAAGTGGAAAGCC	9092
rs34797583	in-del	-/AAACA			upstream-variant-2KB	SART1	GRCh38.p7	11:65961206	AAACAAAACAAAACA[-/AAACA]GGGAACGTGGGAAGG	9092
rs34922998	snp	C/G	0.0298439	0.118454	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966444	GCGGCACGGCTGATG[C/G]CCTGCGGGAGCGGGA	9092
rs34924971	in-del	-/C			intron-variant	SART1	GRCh38.p7	11:65970704	TGGAGAGCAGATACA[-/C]CCTGGGAGAAGAGCA	9092
rs35036096	snp	G/T	0.197531	0.244432	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967544	CCTCAGCCCCTGCCG[G/T]CGGACGACACCCGAG	9092
rs35056344	in-del	-/C			frameshift-variant, nc-transcript-variant	SART1	GRCh38.p7	11:65967698	GGTGGAGCTCCACCG[-/C]CCGGGGTCCCCGCAG	9092
rs35186856	snp	C/T	0.00199787	0.0315427	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65978819	GATGAGCTCCAGCGA[C/T]ACGCCCCTGGGCACC	9092
rs35216160	in-del	-/T			intron-variant	SART1	GRCh38.p7	11:65967967	TTTTTTTTTTTTTTT[-/T]GAGACAGAGTTTCGC	9092
rs35239693	in-del	-/T	0.498734	0.0251279	intron-variant	SART1	GRCh38.p7	11:65970625	CCGATTGTTCTGGTG[-/T]TTTTCCAGTGAAGAG	9092
rs35262635	in-del	-/C			downstream-variant-500B	SART1	GRCh38.p7	11:65980393	TCACCTTGGCTGCTT[-/C]CCTTGGCTTCCTCAG	9092
rs35322123	in-del	-/C			intron-variant	SART1	GRCh38.p7	11:65976330	GAGGACCCTTAGGTT[-/C]CCTGGGTCTCAATGG	9092
rs35807911	in-del	-/G			frameshift-variant, nc-transcript-variant	SART1	GRCh38.p7	11:65967569	CCGAGTGGAGAACAT[-/G]GGACATCAGTGATGA	9092
rs35831021	in-del	-/A	0.0554779	0.157039	utr-variant-3-prime	SART1	GRCh38.p7	11:65980111	GTCAGACCCTGTCTC[-/A]AAAAAAATAAAAAAA	9092
rs35842560	in-del	-/A			frameshift-variant, nc-transcript-variant	SART1	GRCh38.p7	11:65977881	GATGAGACGGGCCGG[-/A]AAACTCACACCCAAG	9092
rs35869960	in-del	-/G			utr-variant-3-prime, downstream-variant-500B	SART1	GRCh38.p7	11:65979433	TGGGGATTGGGCTTT[-/G]GGGTAGGGCACAGGT	9092
rs36014546	in-del	-/C			intron-variant	SART1	GRCh38.p7	11:65978197	CACTGGCTTTCCTGG[-/C]CCCGCAGGGCCATTC	9092
rs55704213	snp	A/C	0.466721	0.124627	intron-variant	SART1	GRCh38.p7	11:65962531	GAATCGTGTAGGGCG[A/C]ATGGTAGAGAAATGA	9092
rs55723810	snp	A/G	0.5	0	intron-variant	SART1	GRCh38.p7	11:65971102	GAGCTGAGGAGGGGG[A/G]TGGTGGGATTCATGA	9092
rs55928757	snp	A/G	0.485118	0.0849685	intron-variant	SART1	GRCh38.p7	11:65974299	GAATCACTTGAACCC[A/G]AGAGGTGGAGGTTGC	9092
rs55992629	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65971095	GATTCATGAGCTGAG[A/G]AGGGGGATGGTGGGA	9092
rs55994535	in-del	-/AA			intron-variant	SART1	GRCh38.p7	11:65974391	AAAAAAAAAAAAAAA[-/AA]CCATATCAGCCGGGT	9092
rs56154109	snp	C/T	0.495056	0.049474	intron-variant	SART1	GRCh38.p7	11:65975367	CTCGGCCTCCCAAAG[C/T]GCTAGGATTATAGAT	9092
rs56159637	in-del	-/C/T			intron-variant	SART1	GRCh38.p7	11:65975431	TTTTTTTTTTTTTTT[-/C/T]CGAGACGGGGTTTCA	9092
rs56239996	snp	A/T	0.466721	0.124627	intron-variant	SART1	GRCh38.p7	11:65962532	AATCGTGTAGGGCGC[A/T]TGGTAGAGAAATGAG	9092
rs56365031	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65971204	GGGATGGTGGGATTC[A/G]TGAGCTG	9092
rs56663613	snp	A/G	0.0240643	0.107019	intron-variant	SART1	GRCh38.p7	11:65966972	CAGCTGGCGCGGTAG[A/G]CGTCTTCCTCAGTGG	9092
rs57209570	in-del	-/CTG			intron-variant	SART1	GRCh38.p7	11:65970881	GGGATTCATGAGCTG[-/CTG]AGGAGGGGGATGGTG	9092
rs57343901	in-del	-/ACAAAA			upstream-variant-2KB	SART1	GRCh38.p7	11:65961209	TCTCAAGGGAAAAAA[-/ACAAAA]CAAAACAAAACAAAA	9092
rs57968007	snp	C/T	0.186421	0.24178	intron-variant	SART1	GRCh38.p7	11:65962209	AAACCCCCAAGCTGT[C/T]TACCAGCTCTATTAA	9092

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