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
rs3057	snp	A/G	0.460813	0.134379	intron-variant	ASAP1	GRCh38.p7	8:130317591	CTGATGGAAGCATCA[A/G]TGATGGATTTGGCTT	50807
rs716077	snp	A/G	0.328616	0.237317	intron-variant	ASAP1	GRCh38.p7	8:130113467	TCATTATAAGAGTAT[A/G]GAAAAATTCCTGAGA	50807
rs749126	snp	A/G	0.233527	0.249457	intron-variant	ASAP1	GRCh38.p7	8:130091180	GTTTACTGGAACCAC[A/G]CCTGGCATACAGTGA	50807
rs752716	snp	C/T	0.0640965	0.167152	intron-variant	ASAP1	GRCh38.p7	8:130079169	cactgcactccagtc[C/T]gggtgacagagaaag	50807
rs754021	snp	C/T	0.333261	0.235728	intron-variant	ASAP1	GRCh38.p7	8:130289527	TCTTAAAGTTTGGAC[C/T]AGTCTGCAAGGTAGC	50807
rs876575	snp	A/G	0.474	0.111014	intron-variant	ASAP1	GRCh38.p7	8:130198605	GGTACTGTATCTAAC[A/G]TATATTATCTAAAGA	50807
rs897050	snp	A/G	0.321053	0.23969	intron-variant	ASAP1	GRCh38.p7	8:130106826	AGTATTCCTGGAGGA[A/G]CAGGAAAGAGAAGTG	50807
rs897052	snp	A/G	0.0509478	0.151255	intron-variant	ASAP1	GRCh38.p7	8:130055461	GGCAAGACCCACTGC[A/G]GGGTACCATACTCAA	50807
rs897053	snp	A/G	0.0517044	0.152246	intron-variant	ASAP1	GRCh38.p7	8:130055739	AGAGAATCATGTAAT[A/G]GGCCTTCAATAGAAA	50807
rs929990	snp	C/T	0.046775	0.145601	intron-variant	ASAP1	GRCh38.p7	8:130264814	AACACACGATGATCA[C/T]TATGTACGCAAAGGG	50807
rs966185	snp	A/G	0.498842	0.0240367	missense	ASAP1	GRCh38.p7	8:130112313	TGCCAGCCAAGCCCT[A/G]TCAAGAAAGAGCGCT	50807
rs1008819	snp	C/T	0.360842	0.224085	intron-variant	ASAP1	GRCh38.p7	8:130263914	TGTCATTATTGTCTA[C/T]GTTACTTTAGACACA	50807
rs1017281	snp	C/T	0.489608	0.0713316	intron-variant	ASAP1	GRCh38.p7	8:130234967	ccacatagtaggtgc[C/T]taacaaatggtagAT	50807
rs1030386	snp	C/T	0.161267	0.233723	intron-variant	ASAP1	GRCh38.p7	8:130311270	TTTTCAAGTTTTCCC[C/T]AATGGCCATATTTTA	50807
rs1031473	snp	A/G	0.0520825	0.152737	intron-variant	ASAP1	GRCh38.p7	8:130067730	AGAATACAGGAAAAC[A/G]CTGGGTTCTTAATGG	50807
rs1031474	snp	A/G	0.39527	0.203462	intron-variant	ASAP1	GRCh38.p7	8:130105751	CACTAGTGTCCCAGC[A/G]CACTCTACTCCACCA	50807
rs1031475	snp	A/T	0.397452	0.201886	intron-variant	ASAP1	GRCh38.p7	8:130105666	TCCTTCTTTGTATAA[A/T]TATACGGTTAATTAC	50807
rs1118887	snp	A/T	0.473266	0.112482	intron-variant	ASAP1	GRCh38.p7	8:130189775	ggaactctcatacgc[A/T]gttggtggtaatata	50807
rs1123205	snp	C/G	0.486855	0.0799975	intron-variant	ASAP1	GRCh38.p7	8:130336864	GAGAAGTAGTTTCTT[C/G]AAATGTTCTCTGGTG	50807
rs1158569	snp	A/C	0.496746	0.040204	intron-variant	ASAP1	GRCh38.p7	8:130318766	TAACTTCAAATATAG[A/C]CTAGACACTTAAAAA	50807
rs1158570	snp	C/T	0.482384	0.0921818	intron-variant	ASAP1	GRCh38.p7	8:130318827	TTGTCAGTGGAAATG[C/T]CAAATGGAGTGGCCA	50807
rs1298714	snp	A/T	0	0	intron-variant	ASAP1	GRCh38.p7	8:130276728	GAGAGAGAGAGAGAG[A/T]GTGTGTGTGTGTGTG	50807
rs1340019	snp	C/T	0.248188	0.249993	intron-variant	ASAP1	GRCh38.p7	8:130343801	TGTCATTGTATTAAA[C/T]GTTTCCCTCCCTCCC	50807
rs1340020	snp	A/C	0.357664	0.225629	intron-variant	ASAP1	GRCh38.p7	8:130343755	TTGTGTGTTTTGTAC[A/C]GTTGGCTTAGCAGTT	50807
rs1340021	snp	C/G	0.49306	0.0584955	intron-variant	ASAP1	GRCh38.p7	8:130337072	GTGAGTCCTGACTGG[C/G]TTAGCTATTTGTGAT	50807
rs1340022	snp	A/G	0.492188	0.0620098	intron-variant	ASAP1	GRCh38.p7	8:130322219	TCAGTTTCTTATGCA[A/G]TTTTTCACTGCATAC	50807
rs1365181	snp	A/G	0.00279162	0.0372561	intron-variant	ASAP1	GRCh38.p7	8:130217861	CTGGGTTATTTCCCA[A/G]TCCAGACTCATGTTC	50807
rs1365182	snp	C/T	0.0532157	0.154195	intron-variant	ASAP1	GRCh38.p7	8:130235257	CTGAAGCCTTGATTG[C/T]GATTTGGAAGAGCAG	50807
rs1417007	snp	C/G	0.333952	0.235483	intron-variant	ASAP1	GRCh38.p7	8:130340340	TAACCTTGTTTGACT[C/G]TTTTGTAGGCTAAAT	50807
rs1417008	snp	G/T	0.226188	0.248863	intron-variant	ASAP1	GRCh38.p7	8:130265006	GACTAAAATTACTGG[G/T]GTACAAGGAAGTGGT	50807
rs1417009	snp	A/T	0.0162398	0.0886349	intron-variant	ASAP1	GRCh38.p7	8:130265080	AGGATGTGGCCCTTT[A/T]CTCATGGCAACAAAG	50807
rs1417010	snp	C/T	0.0154538	0.0865337	intron-variant	ASAP1	GRCh38.p7	8:130268818	CATTTGCAGTCTCCA[C/T]AAAATTATACTACTG	50807
rs1426101	snp	A/G	0.388701	0.211287	intron-variant	ASAP1	GRCh38.p7	8:130230514	AGGGTCAAGGAAGGG[A/G]TTTTTTTCCCCCAAA	50807
rs1426102	snp	C/G	0.24019	0.249807	intron-variant	ASAP1	GRCh38.p7	8:130301123	CCCAGCATAAGCAGA[C/G]GACATGAGAAATAGT	50807
rs1469285	snp	C/T	0	0	intron-variant	ASAP1	GRCh38.p7	8:130217587	AGGTAATCCCTGCCT[C/T]TTGCGGTCTGGTGGT	50807
rs1469286	snp	C/T	0.33533	0.234987	intron-variant	ASAP1	GRCh38.p7	8:130214773	AGAATTCGTAGTGAT[C/T]GGTGTTCAAAGTAAC	50807
rs1469287	snp	C/T	0.00358779	0.0422022	intron-variant	ASAP1	GRCh38.p7	8:130214503	CTTTCCAAAATATTA[C/T]GTCATATAGAGAACA	50807
rs1469288	snp	C/T	0.474363	0.110278	intron-variant	ASAP1	GRCh38.p7	8:130214406	AGTCCTAGGTAACTT[C/T]CACACCTCAACTAAA	50807
rs1538728	snp	C/T	0.497695	0.0338674	intron-variant	ASAP1	GRCh38.p7	8:130336114	CTGTTTCTGAAACTT[C/T]GTTTTGCATTATCTT	50807
rs1549454	snp	A/G	0.357238	0.225832	intron-variant	ASAP1	GRCh38.p7	8:130249740	TACAACTGGGAGGAA[A/G]TAATATATAAATAAA	50807
rs1549455	snp	C/T	0.341685	0.232581	intron-variant	ASAP1	GRCh38.p7	8:130252774	GGAAAATAATAATTA[C/T]AGGTACAACAAGGTA	50807
rs1556972	snp	C/G	0.233527	0.249457	intron-variant	ASAP1	GRCh38.p7	8:130263324	GTCAGATCCCACCCT[C/G]TCAGGAATTTGAACT	50807
rs1801625	snp	A/C			utr-variant-3-prime	ASAP1	GRCh38.p7	8:130052884	AGCCACACCAGTGTC[A/C]GGATGGAAGTCTGCA	50807
rs1815642	snp	A/T	0.0182089	0.0937193	intron-variant	ASAP1	GRCh38.p7	8:130288784	CAGCAGCATTACTTA[A/T]AGAAGAAAAGAAGGG	50807
rs1934563	snp	A/C	0	0	intron-variant	ASAP1	GRCh38.p7	8:130298655	TAATGGGGAACAAGA[A/C]CGGTAATGAGCCTGG	50807
rs1960661	snp	C/T	0.328616	0.237317	intron-variant	ASAP1	GRCh38.p7	8:130189995	CATAGGAAAAAAATC[C/T]AGTTTTAAACTGGGC	50807
rs1974313	snp	A/G	0.336474	0.234568	intron-variant	ASAP1	GRCh38.p7	8:130263069	TTTTTACTAATACGA[A/G]TATGAATTTACTAAT	50807
rs1978550	snp	C/T	0.499121	0.020948	intron-variant	ASAP1	GRCh38.p7	8:130263786	AATAACAACTTCCAG[C/T]GCCTTCTACCAACTA	50807
rs1978551	snp	C/G	0.350546	0.22889	intron-variant	ASAP1	GRCh38.p7	8:130245549	GGTGGTGTTTTCTTG[C/G]ATGGACTAAATCCTT	50807
rs2005040	snp	G/T	0.475081	0.108804	intron-variant	ASAP1	GRCh38.p7	8:130289211	AAGTATAGTTTTTTT[G/T]TTTGTTTGTTTTTGT	50807
rs2009449	snp	G/T	0	0	intron-variant, upstream-variant-2KB	ASAP1, ASAP1-IT1	GRCh38.p7	8:130296884	CCTCTCCCTGGCCAG[G/T]GGTTCTTATTTACTT	50807
rs2027377	snp	A/T	0.342582	0.232225	intron-variant	ASAP1	GRCh38.p7	8:130309403	TTAGTCTAAGTGTCA[A/T]AGCACCCAAAGTCTT	50807
rs2033059	snp	C/T	0.457154	0.139954	intron-variant	ASAP1	GRCh38.p7	8:130258970	CCCTATTTGCCCCAT[C/T]GATTCCAAAAATAAA	50807
rs2045091	snp	A/G	0.318896	0.240319	intron-variant	ASAP1	GRCh38.p7	8:130063613	GGAAGATGAAGCTAC[A/G]TCATGCAGCAGGTCT	50807
rs2045092	snp	A/G	0.498369	0.0285077	intron-variant	ASAP1	GRCh38.p7	8:130063400	TGTGGACAGGGTCTA[A/G]ATACCTGAAGCTGGG	50807
rs2045093	snp	C/T	0.354665	0.227036	intron-variant	ASAP1	GRCh38.p7	8:130079346	AAGGCTGGATAAAAA[C/T]TGCCCGTAAGAGATC	50807
rs2052710	snp	A/C	0.0463947	0.145069	intron-variant	ASAP1	GRCh38.p7	8:130254841	TTTCTTAAGTAGCAA[A/C]AACCAATCTAACAAC	50807
rs2085064	snp	A/C	0	0	intron-variant	ASAP1	GRCh38.p7	8:130090508	AATGAATTAGTTCCC[A/C]CAAGCCAGGCAAGAA	50807
rs2114196	snp	C/T	0.470034	0.11868	intron-variant	ASAP1	GRCh38.p7	8:130213053	CACTTTCACTGGAGG[C/T]CTTGCTCAAAGTGTG	50807
rs2114197	snp	A/G	0.175254	0.238565	intron-variant	ASAP1	GRCh38.p7	8:130244811	TCCAGGATTGCAGGG[A/G]TTAAAGATGGAGATG	50807
rs2123870	snp	G/T	0.476746	0.10529	intron-variant	ASAP1	GRCh38.p7	8:130064174	aacctggtcctgcag[G/T]ctgttctcaacagaa	50807
rs2185366	snp	A/G	0.468949	0.12067	intron-variant	ASAP1	GRCh38.p7	8:130330476	GGTGTTCACAGGTGA[A/G]TGGGGTGGTGGTTGT	50807
rs2303444	snp	C/T	0.219435	0.248125	intron-variant	ASAP1	GRCh38.p7	8:130214506	AGCCTTTCCAAAATA[C/T]TACGTCATATAGAGA	50807
rs2305510	snp	A/C	0.223789	0.248622	intron-variant	ASAP1	GRCh38.p7	8:130126098	GTGGGTTCTGTGGAA[A/C]GAATGTTGAAGACAA	50807
rs2305511	snp	A/C	0.357238	0.225832	intron-variant	ASAP1	GRCh38.p7	8:130126329	AGAAAGGCTTTCCTT[A/C]AGAGACCCTATGCAA	50807
rs2305512	snp	C/T	0.00113632	0.023809	synonymous-codon	ASAP1	GRCh38.p7	8:130115694	CAATCCACACGTCCA[C/T]GTAGAATATGAGTGG	50807
rs2305513	snp	A/G	0.495821	0.0455185	intron-variant	ASAP1	GRCh38.p7	8:130115585	TCAACAACTACCCCA[A/G]CTTTTCTAGTCTGTG	50807
rs2395989	snp	C/T	0.321769	0.239477	intron-variant	ASAP1	GRCh38.p7	8:130068628	ctgcatatgggtata[C/T]atgatccagacacac	50807
rs2395992	snp	A/G	0.164219	0.234823	intron-variant	ASAP1	GRCh38.p7	8:130230846	ATTCTAATCTATTAT[A/G]TCTCTTACATATGCT	50807
rs2396015	snp	C/T			intron-variant	ASAP1	GRCh38.p7	8:130197455	Gttcttttcttttct[C/T]ttttcttttgagaca	50807
rs2554367	snp	A/G	0	0			GRCh38.p7	8:130262482	ATTTCAAATAGGTTA[A/G]ACAGAAGGTTTATTC	50807
rs2554368	snp	A/G					GRCh38.p7	8:130267786	ATATTTTCTCCTTGA[A/G]AAAATCTTCCCGTAA	50807
rs2554369	snp	A/G	0.39527	0.203462			GRCh38.p7	8:130301801	CAGATATGCATATGC[A/G]TTGTTGTTGAGAGTA	50807
rs2554370	snp	A/G					GRCh38.p7	8:130249493	TAAGAAGATGATGGA[A/G]AAAATGGTGAGAGGC	50807
rs2554371	snp	A/G					GRCh38.p7	8:130249202	GACTAGACATATTTA[A/G]AAACACTCTGCAATG	50807
rs2554372	snp	A/G	0.469544	0.119585			GRCh38.p7	8:130321667	TCATTTTATATTTAA[A/G]CAACCATGGAAATAC	50807
rs2554373	snp	A/G	0.486	0.0824865			GRCh38.p7	8:130246289	CCATTGGTACAAAAG[A/G]CAGAGTGGTTTAATG	50807
rs2554374	snp	A/G	0.498908	0.0233371			GRCh38.p7	8:130244152	AATAGGTCTGATACC[A/G]TGCTACCTGTTGGGG	50807
rs2554375	snp	A/G	0	0			GRCh38.p7	8:130284104	GGGTTTTGTCCATTA[A/G]AACCTCTGTCCTCCG	50807
rs2670873	snp	C/T	0.46885	0.12085	intron-variant	ASAP1	GRCh38.p7	8:130316056	AGAGAAAAGCACTTC[C/T]GTCTTTTCAGCTTAA	50807
rs2670874	snp	C/T	0	0	intron-variant	ASAP1	GRCh38.p7	8:130317322	TGATATTCCTCCCTT[C/T]TCAGCCAAAATTGGG	50807
rs2670875	snp	C/T	0	0	intron-variant	ASAP1	GRCh38.p7	8:130262623	GGAAAGTAAGGGGTT[C/T]TTTTAGTCTAAATAT	50807
rs2670876	snp	A/G	0.228842	0.249103	intron-variant	ASAP1	GRCh38.p7	8:130257640	CCAAATTTACCGACT[A/G]TAGATCCCTTTTTTT	50807
rs2670877	snp	A/G	0	0	intron-variant	ASAP1	GRCh38.p7	8:130335769	ATAGTCTGAGGTTAA[A/G]AAAATGTAGCTCAGG	50807
rs2670878	snp	A/G			intron-variant	ASAP1	GRCh38.p7	8:130335786	AAATGTAGCTCAGGA[A/G]AAAATCCTGTGAACA	50807
rs2670879	snp	A/G	0	0	intron-variant	ASAP1	GRCh38.p7	8:130330511	taacagaatgaatta[A/G]acatgctttctgtcc	50807
rs2670880	snp	G/T	0	0	intron-variant	ASAP1	GRCh38.p7	8:130329222	TGGAAAACTTATTTA[G/T]TTAAGTGGCTTAGTG	50807
rs2670881	snp	G/T	0.164219	0.234823	intron-variant	ASAP1	GRCh38.p7	8:130327308	AGCTTGCCCAACAAT[G/T]TTGGTACAACAGTTT	50807
rs2670882	snp	A/G	0.165527	0.235296	intron-variant	ASAP1	GRCh38.p7	8:130325590	CTTTCCTCTTTGTAT[A/G]TCCCAAAACGCCTTC	50807
rs2670883	snp	C/T	0.0107246	0.0724382	intron-variant	ASAP1	GRCh38.p7	8:130324394	AGTTGGTTAATGATA[C/T]TCAACCTTTTCATCC	50807
rs2670884	snp	A/G	0.494143	0.0537956	intron-variant	ASAP1	GRCh38.p7	8:130243588	TGGCTGGAACATAAT[A/G]AGTAGTGGAGGGTGT	50807
rs2670885	snp	A/G	0.403684	0.197183	intron-variant	ASAP1	GRCh38.p7	8:130275862	AACTACATTCCTCAC[A/G]GAGAACAACAGAACT	50807
rs2670886	snp	C/T	0.163892	0.234703	intron-variant	ASAP1	GRCh38.p7	8:130244432	AATCCAAAATGACCA[C/T]GTGGGTACAATAAAC	50807
rs2670887	snp	C/T	0.164219	0.234823	intron-variant	ASAP1	GRCh38.p7	8:130245956	CGGGACTCTTGGAGG[C/T]TACAGTGGTTCCCAA	50807
rs2670888	snp	C/T	0.38934	0.207568	intron-variant	ASAP1	GRCh38.p7	8:130247918	GCATGTGTACCTGCA[C/T]ACAGAAAATAGGCTT	50807
rs2670889	snp	A/G	0	0	intron-variant	ASAP1	GRCh38.p7	8:130303049	TTCCCTTCTGCCTTA[A/G]GTATGGATTCTTTGG	50807
rs2670890	snp	C/T	0.387263	0.208947	intron-variant	ASAP1	GRCh38.p7	8:130302677	CTTGAGATGTCCCCA[C/T]GTGCCCCTCCCCCTC	50807
rs2670891	snp	C/T	0.406123	0.195258	intron-variant	ASAP1	GRCh38.p7	8:130268457	CATGCCATTATACTC[C/T]AGCCTGGGTGACAGA	50807
rs2791338	snp	A/G	0.388587	0.208071	intron-variant	ASAP1	GRCh38.p7	8:130273391	CTGCTTCCACTCAAG[A/G]TCTGCAGAAGGGGAA	50807
rs2791339	snp	C/T	0.135825	0.222405	intron-variant	ASAP1	GRCh38.p7	8:130275688	GAAACGTAAGCATTT[C/T]GATGCTTTTAAAATT	50807

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