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
rs2951	snp	C/T	0.0154538	0.0865337	intron-variant, utr-variant-3-prime	ARHGEF7	GRCh38.p7	13:111280943	TCTTCTAGGGCCACA[C/T]GGAGCAGAAGCAGCT	8874
rs6692	snp	A/G	0.38821	0.208322	utr-variant-3-prime, upstream-variant-2KB	ARHGEF7, TEX29	GRCh38.p7	13:111305522	TGCTTGTCCACATGC[A/G]CTGGGCGTCTGGGAC	8874
rs748421	snp	A/C	0.0023933	0.0345097	intron-variant	ARHGEF7	GRCh38.p7	13:111122942	ccagggccgcctCCC[A/C]GCACAGGCCTTGGAG	8874
rs755029	snp	C/T	0.450985	0.148678	intron-variant	ARHGEF7	GRCh38.p7	13:111199154	GTGGCCAGGCCTGCC[C/T]CTGCCTGTAGGAAGC	8874
rs831140	snp	A/G	0.0182019	0.0936463	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	ARHGEF7, ARHGEF7-AS2	GRCh38.p7	13:111114877	CGTTTGTTTCGCTTT[A/G]CTACCTTGCAAGCCG	8874
rs831143	snp	A/G	0.089084	0.191327	intron-variant, upstream-variant-2KB	ARHGEF7, ARHGEF7-AS2	GRCh38.p7	13:111116495	ACATCGTTTTTAGAA[A/G]CTCTCCTGCCTCCTC	8874
rs831144	snp	A/C	0.0256215	0.110247	intron-variant	ARHGEF7	GRCh38.p7	13:111118399	GGAATTATAAACTTT[A/C]CATGAACAGTTCAGA	8874
rs831145	snp	A/G	0.0825414	0.185628	intron-variant	ARHGEF7	GRCh38.p7	13:111119024	CCCTGCAGGTACCTT[A/G]ATCCCAGACTTTGGG	8874
rs831146	snp	C/G	0.280256	0.248162	intron-variant	ARHGEF7	GRCh38.p7	13:111120218	AGTGAGCCAGCAAAT[C/G]CAGTTCCAGCTACCT	8874
rs831147	snp	A/G	0.343924	0.231686	intron-variant	ARHGEF7	GRCh38.p7	13:111120423	AACTTATGCACACAC[A/G]CATGCATGCCTGCAC	8874
rs831148	snp	A/G	0.0232847	0.105357	intron-variant	ARHGEF7	GRCh38.p7	13:111120472	tctgtgtgtgtgtgt[A/G]tttacatgcatgtgt	8874
rs831149	snp	C/T	0.157642	0.232314	intron-variant	ARHGEF7	GRCh38.p7	13:111120786	GCAGCATGCTCCTCT[C/T]GTTTGCAGGCGCTGT	8874
rs831150	snp	C/G	0.472429	0.114129	intron-variant	ARHGEF7	GRCh38.p7	13:111120969	ACTTAGGGGAAGATT[C/G]GCAACCACTGCCTTC	8874
rs831151	snp	C/G	0.0825414	0.185628	intron-variant	ARHGEF7	GRCh38.p7	13:111121072	TGAGGACTGGAGGGG[C/G]TGGCTCAGGTCACCG	8874
rs831152	snp	A/G	0.316	0.241131	intron-variant	ARHGEF7	GRCh38.p7	13:111121182	GCTCTGCCCTTCAGT[A/G]GACAGACCCCAAAGG	8874
rs831153	snp	C/T	0.0825414	0.185628	intron-variant	ARHGEF7	GRCh38.p7	13:111121329	TAACTCACTGTAGTT[C/T]CTGGGCTTCCCTACT	8874
rs831154	snp	C/G	0.251296	0.249997	intron-variant	ARHGEF7	GRCh38.p7	13:111121800	AGACAGGTGCCGGAA[C/G]TCACAGAGCAAATGG	8874
rs831155	snp	C/T	0.251578	0.249995	intron-variant	ARHGEF7	GRCh38.p7	13:111121941	AAACAGTAACTACTG[C/T]GTACTGAGGAATGAC	8874
rs831156	snp	C/T	0.00676609	0.0577691	intron-variant	ARHGEF7	GRCh38.p7	13:111121995	CTTGGCTTACAGTCT[C/T]CTGGACACGATGGGG	8874
rs831157	snp	A/G	0.168785	0.236441	intron-variant	ARHGEF7	GRCh38.p7	13:111122521	ATCCTGCAAAAACAG[A/G]GTTGAGAACTGCCAG	8874
rs831158	snp	A/G	0.00676609	0.0577691	intron-variant	ARHGEF7	GRCh38.p7	13:111122657	AGCACGCACACAATA[A/G]GAACCTGGTAAAAGG	8874
rs831159	snp	A/T	0.274661	0.248781	intron-variant	ARHGEF7	GRCh38.p7	13:111130530	CTGTCAATAAATCAC[A/T]TCCCCTAATAAAACA	8874
rs831160	snp	C/G	0.0170251	0.090679	intron-variant	ARHGEF7	GRCh38.p7	13:111130879	GAAGGGCCCCTCTGT[C/G]TAGGGGTGCATGCCC	8874
rs831161	snp	C/T	0.375	0.216506	intron-variant	ARHGEF7	GRCh38.p7	13:111131028	TGGGCCCTTAGTTTG[C/T]AAAGGTTTTGATACT	8874
rs831162	snp	A/G	0.421368	0.182025	intron-variant	ARHGEF7	GRCh38.p7	13:111131339	CCAGCACAGGCGACC[A/G]CCCCATCTATCCTGT	8874
rs831163	snp	C/T	0.327211	0.237778	intron-variant	ARHGEF7	GRCh38.p7	13:111132211	AAGGAAAAGAACACA[C/T]TTTAAAATGTGGGAA	8874
rs831164	snp	G/T	0.0364509	0.129988	intron-variant	ARHGEF7	GRCh38.p7	13:111139910	TCTCAACAGGGAGGG[G/T]TGAAACTTTTAAGGT	8874
rs831165	snp	A/G	0.34526	0.23114	intron-variant	ARHGEF7	GRCh38.p7	13:111139949	GACAATCTTTCATTT[A/G]TCTCTCACTTTGTCT	8874
rs831166	snp	G/T	0.4941	0.0539917	intron-variant	ARHGEF7	GRCh38.p7	13:111143032	GGAGCTGGGTGGCAG[G/T]AGGACACTTCAGAAG	8874
rs831167	snp	C/T	0.210301	0.246828	intron-variant	ARHGEF7	GRCh38.p7	13:111143197	TGGTCAAGAATAGGA[C/T]ATTGGGTTATTGGTG	8874
rs831168	snp	A/G	0.490398	0.0686206	intron-variant	ARHGEF7, ARHGEF7-AS1	GRCh38.p7	13:111144626	TGTAATTAAAAATTA[A/G]ATGAACCATTGAATG	8874
rs831169	snp	A/G	0.209388	0.246679	intron-variant	ARHGEF7, ARHGEF7-AS1	GRCh38.p7	13:111145573	AGGGGTGGCCCTGGC[A/G]TGTACCGTTTGCTGA	8874
rs860520	snp	G/T	0.333722	0.235565	intron-variant	ARHGEF7	GRCh38.p7	13:111133658	ggtttgtaaatttgg[G/T]tgtatgtgagactgc	8874
rs880248	snp	C/T	0.0103295	0.0711199	intron-variant	ARHGEF7	GRCh38.p7	13:111247958	GTGCGTTCTGAGGCC[C/T]ATGTTTGTTTTCTCA	8874
rs882700	snp	C/T	0.154661	0.231107	intron-variant	ARHGEF7, ARHGEF7-AS1	GRCh38.p7	13:111145084	CCACGGTGTTCCCCA[C/T]GTTCCCTACCACACC	8874
rs883788	snp	C/T	0.450859	0.148847	intron-variant	ARHGEF7	GRCh38.p7	13:111230767	AAGGTGTCAAGATCA[C/T]GTTCCCCAGAACACC	8874
rs942648	snp	C/T	0.109461	0.206758	intron-variant	ARHGEF7	GRCh38.p7	13:111298964	CTCATTTTCCATTAT[C/T]GGTGTGGCAAGTGTC	8874
rs942649	snp	C/T	0.129664	0.219133	intron-variant	ARHGEF7	GRCh38.p7	13:111302209	CAAGGGTGTTCTGGG[C/T]ATTGCACGGAATGTG	8874
rs942651	snp	C/T	0.000399281	0.0141238	intron-variant	ARHGEF7	GRCh38.p7	13:111187486	AGGAAATTATTGGTT[C/T]GCACAACAAACAAGT	8874
rs942652	snp	A/G	0.117537	0.212022	intron-variant, upstream-variant-2KB, utr-variant-5-prime	ARHGEF7	GRCh38.p7	13:111184808	GAAGCCCACGGGGCC[A/G]GTAACCCACACACAG	8874
rs942653	snp	C/T	0.484632	0.086302	intron-variant	ARHGEF7	GRCh38.p7	13:111181684	CAGTGCACTGTTCCA[C/T]GATGCCTCAGGGCAC	8874
rs942654	snp	A/G	0	0	intron-variant	ARHGEF7	GRCh38.p7	13:111276260	GTAGAATAAAATTCA[A/G]AAAGAGGTGCCTGTT	8874
rs942655	snp	A/G	0.330846	0.236567	intron-variant	ARHGEF7	GRCh38.p7	13:111241362	GGCCTTCCTGACCTC[A/G]GGGCGCAGCCGGGGG	8874
rs942656	snp	A/T	0.222035	0.248431	intron-variant	ARHGEF7	GRCh38.p7	13:111236479	aacagcaacagtata[A/T]cccaggggaggtgga	8874
rs1096481	snp	C/G	0.347914	0.230028	intron-variant	ARHGEF7	GRCh38.p7	13:111134746	cattctgtaggttgc[C/G]tgttcactctgatgg	8874
rs1106830	snp	A/C	0.478768	0.100824	intron-variant	ARHGEF7	GRCh38.p7	13:111200165	CAGCCCAAGGCTGGT[A/C]AGGACCCCTCCCATC	8874
rs1108891	snp	A/C	0.406468	0.194981	intron-variant	ARHGEF7	GRCh38.p7	13:111248762	TTGCTAAAGGATATA[A/C]AGAAAAATATTCTTG	8874
rs1109827	snp	A/G	0.253824	0.249971	intron-variant	ARHGEF7	GRCh38.p7	13:111156578	AAGCCAGAGCTGGAT[A/G]CATAGCATACAAAAT	8874
rs1109828	snp	A/C	0.254944	0.249951	intron-variant	ARHGEF7	GRCh38.p7	13:111156566	GATGCATAGCATACA[A/C]AATGACTTCTCAGGG	8874
rs1122887	snp	C/T	0.084728	0.187577	intron-variant, upstream-variant-2KB	ARHGEF7, LOC101060553	GRCh38.p7	13:111154384	TGACCCAGACCTAGA[C/T]GCCAGCCCTTAGATG	8874
rs1164263	snp	A/G	0	0	intron-variant	ARHGEF7	GRCh38.p7	13:111178252	CCTGTTCTCTCGCTG[A/G]TTCCCAGGACATAAG	8874
rs1164264	snp	C/T	0.0150606	0.0854603	intron-variant	ARHGEF7	GRCh38.p7	13:111176270	TAGCAGCAATGGTCG[C/T]ATTTTCTATGGGTAA	8874
rs1164265	snp	A/G	0.0275645	0.114116	intron-variant	ARHGEF7	GRCh38.p7	13:111174584	AGTGAACTAAGCCAC[A/G]TATGCCCAGATAATG	8874
rs1164266	snp	G/T	0.0217236	0.101931	intron-variant	ARHGEF7	GRCh38.p7	13:111174104	GAAATAAGCTAACAC[G/T]GATTCTACCTTGTTT	8874
rs1164267	snp	C/T	0.158962	0.232835	intron-variant	ARHGEF7	GRCh38.p7	13:111218375	CACAAGCCTCAAAAT[C/T]GGAAAGTCAGTGAAA	8874
rs1164268	snp	C/T	0.000399281	0.0141238	intron-variant	ARHGEF7	GRCh38.p7	13:111216720	CCGGCCACCCCTCTT[C/T]CCTACCACTGATGGT	8874
rs1164269	snp	A/G	0.000399281	0.0141238	intron-variant	ARHGEF7	GRCh38.p7	13:111205756	CCTTATCATGGTCAC[A/G]GCTCAAAACTTCTGC	8874
rs1164270	snp	A/G	0.432944	0.170387	intron-variant, upstream-variant-2KB	ARHGEF7	GRCh38.p7	13:111201846	CCATGGTCTAACACT[A/G]AACCGCACAACACAA	8874
rs1164271	snp	G/T	0.325327	0.238382	intron-variant, upstream-variant-2KB	ARHGEF7	GRCh38.p7	13:111201704	TAGACCTCAGACTTC[G/T]CATCCTCACCAGGGA	8874
rs1164272	snp	C/T	0.0185938	0.0946107	intron-variant	ARHGEF7	GRCh38.p7	13:111230208	TGCCCCAGTCAGCCC[C/T]TGGAAAGGTAGCACT	8874
rs1164273	snp	A/G	0.0185938	0.0946107	intron-variant, upstream-variant-2KB	ARHGEF7	GRCh38.p7	13:111186745	CTCGCCTCCTCCAGG[A/G]ACTTGAGAAAGTTAT	8874
rs1359429	snp	A/G	0.499203	0.0199521	intron-variant	ARHGEF7	GRCh38.p7	13:111252977	TGGCTGGGGGCTCTC[A/G]CTGGGGCTGCCTTAG	8874
rs1408725	snp	C/G	0.180702	0.240204	intron-variant	ARHGEF7	GRCh38.p7	13:111253085	CACTAAGGCTTTCTT[C/G]TCCCAAAGTGAGGCA	8874
rs1536046	snp	G/T	0.165853	0.235413	intron-variant	ARHGEF7	GRCh38.p7	13:111177311	ATAACACAACATCAT[G/T]TGTGTTTCTTCAATA	8874
rs1536048	snp	A/G	0.464309	0.12873	intron-variant	ARHGEF7	GRCh38.p7	13:111234289	GTGGCACAGCTCCAC[A/G]TGGTGGAGCTGCTCA	8874
rs1555751	snp	C/T	0.121776	0.214613	utr-variant-3-prime	ARHGEF7	GRCh38.p7	13:111303118	CCAATCTATAAGGGA[C/T]GTCCTCAGTTCTTTC	8874
rs1555753	snp	A/G	0.176219	0.238865	intron-variant	ARHGEF7	GRCh38.p7	13:111262245	tttaaaatcagaaac[A/G]aaaaagaaaaattat	8874
rs1555754	snp	A/C	0.209693	0.246729	intron-variant	ARHGEF7	GRCh38.p7	13:111242324	CAACCCGGGTCGTTA[A/C]TCTGTTTGCCTACTG	8874
rs1555755	snp	C/T	0.278399	0.248382	intron-variant, upstream-variant-2KB	ARHGEF7	GRCh38.p7	13:111232605	CTCCAGCAAGGATTC[C/T]GATGTTTTAAAACAG	8874
rs1557247	snp	A/G	0.343254	0.231956	intron-variant, upstream-variant-2KB	ARHGEF7, LOC101060553	GRCh38.p7	13:111155301	GATTTGATGTTCTAG[A/G]TTTTCCGAGAAACCT	8874
rs1658728	snp	G/T	0	0	intron-variant, upstream-variant-2KB, nc-transcript-variant	ARHGEF7, LOC101060553	GRCh38.p7	13:111152483	TATGGAAACATGTCA[G/T]CACTTGCTTGAATGA	8874
rs1803501	snp	C/T			utr-variant-3-prime, upstream-variant-2KB	ARHGEF7, TEX29	GRCh38.p7	13:111305374	TTTGCCCGAGGGTTA[C/T]TCCTTTGCTCTCACC	8874
rs1854965	snp	C/T	0.446641	0.154377	intron-variant, upstream-variant-2KB	ARHGEF7, ARHGEF7-AS2	GRCh38.p7	13:111117005	TCAGCTCCTGCTCCT[C/T]AGTCCTCCTGTCTTA	8874
rs1886555	snp	G/T	0.262159	0.249704	intron-variant, upstream-variant-2KB	ARHGEF7	GRCh38.p7	13:111202570	TCCCCACCATGACTT[G/T]CTGGGTGCTTTAGCA	8874
rs1886559	snp	C/T	0	0	intron-variant	ARHGEF7	GRCh38.p7	13:111278614	AACAAACTACAGCCT[C/T]ACTTTCCTGAGTCTG	8874
rs1888846	snp	A/G	0.0154538	0.0865337			GRCh38.p7	13:111123496	ATGGCACGGGCATGT[A/G]TGTGTGTGTGTGTGA	8874
rs1891957	snp	C/T					GRCh38.p7	13:111184865	TCTAGAGCCCTCCAT[C/T]CGGTTCTCCCCACCT	8874
rs1891958	snp	C/T	0.256061	0.249927			GRCh38.p7	13:111165318	GGCCAGGCATGAACA[C/T]CTACTAAGGGATCTG	8874
rs1891959	snp	C/T	0.0146672	0.084371			GRCh38.p7	13:111162664	GGAAGATGAGTGTTT[C/T]AGAAACAGGTAAGGC	8874
rs1891960	snp	A/G	0.343701	0.231776			GRCh38.p7	13:111157561	TTCTTTTTTTGAGAC[A/G]GAGTTTTGCTCTGTT	8874
rs1891961	snp	A/G	0.253824	0.249971			GRCh38.p7	13:111157189	TTTCCAAATTTCAAA[A/G]TTTTCCAGCTTAAAA	8874
rs1891962	snp	A/G	0.257176	0.249897			GRCh38.p7	13:111157181	TTTCAAAGTTTTCCA[A/G]CTTAAAACCCAGTGC	8874
rs1891963	snp	A/C	0.343477	0.231866			GRCh38.p7	13:111157116	ATATTCCTTTAAAAC[A/C]AATTTATAAAAATAT	8874
rs1969861	snp	A/G	0.379158	0.214052	intron-variant	ARHGEF7	GRCh38.p7	13:111177052	ATAAGTCAGTCagcc[A/G]ggcgcggtggctcac	8874
rs2002308	snp	A/G	0.0988009	0.199095	intron-variant	ARHGEF7	GRCh38.p7	13:111200121	AGGTGATGTCCACAG[A/G]CACAGAAAGATGGTA	8874
rs2003030	snp	A/G	0.32885	0.23724	intron-variant	ARHGEF7	GRCh38.p7	13:111155915	ACCCTGTCTATACTT[A/G]AACAAACCCAAAAAC	8874
rs2027581	snp	A/T	0.314544	0.241524	intron-variant	ARHGEF7	GRCh38.p7	13:111200701	GGTGTTGAGACATCA[A/T]TACTAACCTTGTCAT	8874
rs2038821	snp	A/T	0.267908	0.249358	intron-variant	ARHGEF7	GRCh38.p7	13:111236975	GTCAGAGGTGTTTTT[A/T]GGTTTTTTAGGGACA	8874
rs2038822	snp	C/G	0.255224	0.249945	intron-variant	ARHGEF7	GRCh38.p7	13:111289259	atcacctgaggtcag[C/G]agttcaagaccagcc	8874
rs2057574	snp	A/C	0.221439	0.248363	intron-variant	ARHGEF7	GRCh38.p7	13:111282541	ACGTTTACCATCTGG[A/C]TCTTTACTGAACACT	8874
rs2065422	snp	A/G	0.126909	0.217598	intron-variant	ARHGEF7	GRCh38.p7	13:111122820	TCTGCAAAAGGAGGC[A/G]TCTGGGCTGGATGAC	8874
rs2083172	snp	C/T			intron-variant, downstream-variant-500B	ARHGEF7, ARHGEF7-AS1, LOC101060553	GRCh38.p7	13:111147898	gagacggggtttcac[C/T]gttttagccgggatg	8874
rs2083173	snp	A/G	0.476052	0.106772	intron-variant, downstream-variant-500B	ARHGEF7, ARHGEF7-AS1, LOC101060553	GRCh38.p7	13:111147933	CGATCTCCTGACCTC[A/G]TGATCCGCCCGCCTC	8874
rs2083174	snp	C/T	0.493107	0.0583	intron-variant, downstream-variant-500B	ARHGEF7, ARHGEF7-AS1, LOC101060553	GRCh38.p7	13:111147988	aggcgtgagccaccg[C/T]gcccagccGAGGTCA	8874
rs2094009	snp	C/T	0.298144	0.245321	intron-variant	ARHGEF7	GRCh38.p7	13:111207084	CACTTCTGTACATCA[C/T]CTGTTGCAGTATTTC	8874
rs2096321	snp	C/T	0.16846	0.236329	intron-variant	ARHGEF7	GRCh38.p7	13:111208039	AAGAAAACGTACGGG[C/T]ATTGCCTTCCCACTG	8874
rs2147682	snp	C/T	0.0325976	0.123435	intron-variant	ARHGEF7	GRCh38.p7	13:111190255	CTCCCCTTTCTAGGT[C/T]CCGTGGCAGCCATCT	8874
rs2147684	snp	A/G	0.187053	0.241946	intron-variant	ARHGEF7	GRCh38.p7	13:111215564	acgtggctctgctcc[A/G]aatattattcgcctc	8874
rs2147685	snp	C/T			intron-variant	ARHGEF7	GRCh38.p7	13:111215167	atgcccccagttact[C/T]tgatatgattatgac	8874
rs2147686	snp	G/T	0.321292	0.23962	intron-variant	ARHGEF7	GRCh38.p7	13:111215154	CTCTGATATGATTAT[G/T]ACGCATTGTATGTCT	8874

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