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
rs577	snp	C/T	0.372189	0.218105	utr-variant-3-prime	SNX9	GRCh38.p7	6:157944003	GACCAGCGCCCTTCC[C/T]GACTACATCCGAAAC	51429
rs15371	snp	A/C	0	0	utr-variant-3-prime	SNX9	GRCh38.p7	6:157944076	CAAGGTCCTGTTTTG[A/C]TTTATGCCGTTAAGT	51429
rs168455	snp	C/T	0.434398	0.168811	intron-variant	SNX9	GRCh38.p7	6:157773121	TTAGGAGAGTAAACA[C/T]GAAACAATGGAGGCT	51429
rs181275	snp	A/G	0.0310518	0.120672	intron-variant	SNX9	GRCh38.p7	6:157779546	CATACAGTTGTCTGC[A/G]TAGACCCTTCCCCAC	51429
rs183030	snp	C/T	0.441158	0.161117	intron-variant	SNX9	GRCh38.p7	6:157771845	gggaatggtggtggg[C/T]gcctgtaatcccagc	51429
rs189513	snp	C/T	0.244776	0.249945	intron-variant	SNX9	GRCh38.p7	6:157771749	tgatgccactgtact[C/T]cagcctgggtgacag	51429
rs240641	snp	A/G	0.390277	0.206936	intron-variant	SNX9	GRCh38.p7	6:157770513	AGCGTGAGCCACCGC[A/G]CCCGGCCAATAAATC	51429
rs240642	snp	A/C	0.481319	0.0948228	intron-variant	SNX9	GRCh38.p7	6:157776294	TGCCCATGGAGGAAC[A/C]TCAGGCTGGATGGTG	51429
rs352193	snp	C/T	0.479421	0.0993283	intron-variant	SNX9	GRCh38.p7	6:157772632	agaaatgtattctcc[C/T]ccagttctgaaggct	51429
rs352194	snp	A/T	0.294576	0.245994	intron-variant	SNX9	GRCh38.p7	6:157777661	TTTAGCAGTAAAGTA[A/T]TTCCTAAAATGGGGA	51429
rs352195	snp	A/C	0.0295035	0.117819	intron-variant	SNX9	GRCh38.p7	6:157777621	TGATGATAAATACTG[A/C]AACTTGACCCTTCAG	51429
rs352196	snp	A/G	0.0158469	0.0875917	intron-variant	SNX9	GRCh38.p7	6:157777262	ctcccaagtagctgg[A/G]actacaggcacccgc	51429
rs481907	snp	A/G	0.375	0.216506	intron-variant	SNX9	GRCh38.p7	6:157771722	ACAGAGTGAGACTCC[A/G]TCTTAAAAAAAAAAA	51429
rs582574	snp	A/G	0.355096	0.226837	intron-variant	SNX9	GRCh38.p7	6:157757282	TTTGTATGAGGTATG[A/G]GGTGGCTACTTGTGG	51429
rs589810	snp	A/C	0.499928	0.00598999	intron-variant	SNX9	GRCh38.p7	6:157748868	TTAATATGTTTCATT[A/C]TAATATCAACATCCT	51429
rs591774	snp	A/C	0.337841	0.23406	intron-variant	SNX9	GRCh38.p7	6:157732897	tgccatccttgcccc[A/C]gcccttggcaaccac	51429
rs591864	snp	C/T	0.261056	0.249755	intron-variant	SNX9	GRCh38.p7	6:157732966	TACATTTAAGTGAGA[C/T]CGTACAGTATGTGTC	51429
rs593439	snp	A/C	0.326976	0.237854	intron-variant	SNX9	GRCh38.p7	6:157716308	ACCCAAATGTTTAAA[A/C]AACCATCATGCCGGC	51429
rs595436	snp	A/C	0.499872	0.0079862	intron-variant	SNX9	GRCh38.p7	6:157742175	TCTTTTGTTCCAAGT[A/C]ACACTGTCTGCAAAA	51429
rs595911	snp	A/C	0.499872	0.0079862	intron-variant	SNX9	GRCh38.p7	6:157742238	GTCCATCACCCTTAC[A/C]TGCCCTCACTCTCAG	51429
rs596121	snp	C/G	0.352721	0.227922	intron-variant	SNX9	GRCh38.p7	6:157757972	ggccaggagtttgag[C/G]agcttgggcaacata	51429
rs597619	snp	A/G	0.292523	0.246357	intron-variant	SNX9	GRCh38.p7	6:157758342	TGCCAAGGAGGCTAG[A/G]TGTTACATGGAATGC	51429
rs598303	snp	A/C	0.318174	0.240525	intron-variant	SNX9	GRCh38.p7	6:157736233	agcattgaaactata[A/C]attactttggtcagt	51429
rs598400	snp	A/G	0.352504	0.228019	intron-variant	SNX9	GRCh38.p7	6:157758455	ATGGAGAATGGATTC[A/G]AGAGCGGCAAGTCTG	51429
rs598898	snp	C/T	0.354881	0.226936	intron-variant	SNX9	GRCh38.p7	6:157758609	ACAGATCAAATCTAC[C/T]AACTAAACAATGGTA	51429
rs599898	snp	A/G	0.305685	0.24372	intron-variant	SNX9	GRCh38.p7	6:157729950	atttgcctgttctag[A/G]tatttcatgtcagtg	51429
rs603514	snp	C/T	0.325016	0.242999	intron-variant	SNX9	GRCh38.p7	6:157733201	TTTGCCTGGTGGGGC[C/T]GGGCGCTGTGGCTCA	51429
rs607256	snp	C/T	0.498693	0.0255257	intron-variant	SNX9	GRCh38.p7	6:157745974	TGTAAACACATTACA[C/T]AAATGCTGTTATTCT	51429
rs613350	snp	A/G	0.318174	0.240525	intron-variant	SNX9	GRCh38.p7	6:157737260	cctctggtataattc[A/G]gctgtgaatccgtct	51429
rs614016	snp	A/G	0.359575	0.224707	intron-variant	SNX9	GRCh38.p7	6:157722201	AGAAAAAATCACCCC[A/G]TTTTCAGCTTAGGGT	51429
rs614079	snp	A/G	0.359152	0.224913	intron-variant	SNX9	GRCh38.p7	6:157722150	CACTTCACCTCTATA[A/G]CCTGGGAGCATCTGC	51429
rs617017	snp	A/G	0.499918	0.00638925	intron-variant	SNX9	GRCh38.p7	6:157740528	CCCAATGCAGAGGGG[A/G]CAAATGACTGGGTCC	51429
rs617663	snp	C/T	0.474903	0.109173	intron-variant	SNX9	GRCh38.p7	6:157727921	TAGACACCCCTGCTT[C/T]GGTCTTTTGTCCATC	51429
rs619349	snp	A/G	0.264632	0.249571	intron-variant	SNX9	GRCh38.p7	6:157746365	TTTCCCCTTTAAAAA[A/G]AAAAACATTAAAATG	51429
rs621821	snp	G/T	0.334642	0.235236	intron-variant	SNX9	GRCh38.p7	6:157717985	ctccagtgtctatta[G/T]ttccctctgtatgtc	51429
rs632536	snp	A/G	0.499977	0.00339449	intron-variant	SNX9	GRCh38.p7	6:157741653	AATTAGCCTTGTTCC[A/G]TTAAAAATGATTAAG	51429
rs633499	snp	C/G	0.287606	0.247155	intron-variant	SNX9	GRCh38.p7	6:157741901	CCAGGTGGGACCTGA[C/G]TCTTCATTAATCCAG	51429
rs633620	snp	A/G	0.319616	0.240112	intron-variant	SNX9	GRCh38.p7	6:157753841	aatatacgcagagcc[A/G]gctgtatgggagact	51429
rs638616	snp	C/G	0.499839	0.00898417	intron-variant	SNX9	GRCh38.p7	6:157735038	gcactttgggaggcc[C/G]aggtgggtggatcac	51429
rs641971	snp	C/T	0.286042	0.247388	intron-variant	SNX9	GRCh38.p7	6:157752721	gtagaagaggaaggc[C/T]tctttgcagttgaga	51429
rs646100	snp	C/T	0.474992	0.108989	intron-variant	SNX9	GRCh38.p7	6:157726189	ccaacaggaaacaca[C/T]agagaaagaaGAATT	51429
rs649262	snp	A/G	0.317692	0.240661	intron-variant	SNX9	GRCh38.p7	6:157748502	TTGGGAGGCCAAGGC[A/G]GGTGGGTCACAAGGT	51429
rs649918	snp	C/G	0.499853	0.008585	intron-variant	SNX9	GRCh38.p7	6:157735316	ATTCCAGGGTTGTCT[C/G]CATCCTGACAAACTA	51429
rs650814	snp	A/G	0.498481	0.027514	intron-variant	SNX9	GRCh38.p7	6:157735460	ctttgggaggctgaa[A/G]tgggtggatcacttg	51429
rs653075	snp	A/G	0.384785	0.210554	intron-variant	SNX9	GRCh38.p7	6:157768085	AGTCCCAGGTGAACT[A/G]GGACAGTTGGCCACC	51429
rs656405	snp	A/G	0.499918	0.00638925	intron-variant	SNX9	GRCh38.p7	6:157740013	aagtgacaggttgat[A/G]ggtgcagcaaaccac	51429
rs659978	snp	A/G	0.317933	0.240593	intron-variant	SNX9	GRCh38.p7	6:157740834	ATGGGaagaatgcag[A/G]ccttccaattagatg	51429
rs661961	snp	C/T	0.499831	0.00918375	intron-variant	SNX9	GRCh38.p7	6:157733254	GGAGGCCGAGGCAAG[C/T]GGATCACGAGGTCAG	51429
rs662006	snp	A/G	0.318415	0.240457	intron-variant	SNX9	GRCh38.p7	6:157733282	CAGGAGATCGAGACC[A/G]TCCTGGCAAACACGG	51429
rs662012	snp	C/G	0.352504	0.228019	intron-variant	SNX9	GRCh38.p7	6:157758541	CCTGGGGAAAAGACA[C/G]TCTTGGTGGGGGCAG	51429
rs662413	snp	A/G	0.499853	0.008585	intron-variant	SNX9	GRCh38.p7	6:157733357	TGGGGGCGGGTGCCT[A/G]TAGTCCCAGCTACTC	51429
rs668360	snp	A/C	0.319856	0.240042	intron-variant	SNX9	GRCh38.p7	6:157717478	GAGGAGGGAGAAGTA[A/C]CCCCTTCTCCCACAC	51429
rs670936	snp	A/G	0.499923	0.00618962	intron-variant	SNX9	GRCh38.p7	6:157740942	caaaatggagggaat[A/G]acatctacttcataa	51429
rs671869	snp	C/T	0.499853	0.008585	intron-variant	SNX9	GRCh38.p7	6:157741162	gaccagcctggccaa[C/T]gtggcaaaatcccgt	51429
rs673376	snp	C/T	0.274661	0.248781	upstream-variant-2KB, nc-transcript-variant	SNX9, LOC107986663	GRCh38.p7	6:157714707	CTGGATATCCCAAGG[C/T]GAAGTGGCCTTCCAT	51429
rs675650	snp	A/G	0.284733	0.247575	intron-variant	SNX9	GRCh38.p7	6:157756299	GTGCCTGTAGACCCA[A/G]GTACTTGGGGGGCTG	51429
rs677742	snp	C/T	0.317933	0.240593	intron-variant	SNX9	GRCh38.p7	6:157734503	CATTAGCTTCTCAGC[C/T]GGGAGGCAGCAGCAC	51429
rs678923	snp	A/G			intron-variant	SNX9	GRCh38.p7	6:157750514	gaaacccaaaactgt[A/G]aaactcctttaagaa	51429
rs683750	snp	C/T	0.317692	0.240661	intron-variant	SNX9	GRCh38.p7	6:157748037	TTGAACCCAAGCAGT[C/T]TGAGAATTGAATCAA	51429
rs684340	snp	A/G	0.286303	0.24735	intron-variant	SNX9	GRCh38.p7	6:157748231	TAGATCTAACAGTAT[A/G]AGGACTCTGTATCTA	51429
rs686943	snp	C/T	0.49889	0.0235361	intron-variant	SNX9	GRCh38.p7	6:157748798	TCTCATTTTCATTCT[C/T]AAACAGTCTTTTCTC	51429
rs688728	snp	A/G	0.284733	0.247575	intron-variant	SNX9	GRCh38.p7	6:157756867	TCAGCAACAAAGCAG[A/G]CTGTGCCAACCTGCG	51429
rs722349	snp	A/G	0	0	intron-variant	SNX9	GRCh38.p7	6:157899442	AAATGCAGACTGTAA[A/G]AATGTTAAGTGGTAC	51429
rs724897	snp	G/T	0.346811	0.230494	intron-variant	SNX9	GRCh38.p7	6:157936169	TTTCTGTGTATCTTT[G/T]TTAATTGTGTTTAAT	51429
rs766595	snp	A/G	0.356597	0.226135	intron-variant	SNX9	GRCh38.p7	6:157787479	TGTGTGTGTGTGTGT[A/G]TATTTGTGTGTATAT	51429
rs766596	snp	A/G	0.300926	0.244758	intron-variant	SNX9	GRCh38.p7	6:157787514	ACACAtatatagtac[A/G]tatatattttttctg	51429
rs827517	snp	A/G	0.499913	0.00658888	intron-variant	SNX9	GRCh38.p7	6:157752055	aataagctgggcatg[A/G]tgtcacatgcctgta	51429
rs827521	snp	C/T	0.318174	0.240525	intron-variant	SNX9	GRCh38.p7	6:157739481	atggagaaataggaa[C/T]gcttttacactgttg	51429
rs827522	snp	G/T	0.499918	0.00638925	intron-variant	SNX9	GRCh38.p7	6:157739636	tcattctactataaa[G/T]acacatgcacatgta	51429
rs844134	snp	C/T	0.476746	0.10529	intron-variant	SNX9	GRCh38.p7	6:157760016	gggactacaggcgtg[C/T]accaccacactggct	51429
rs844135	snp	A/G	0.499839	0.00898417	intron-variant	SNX9	GRCh38.p7	6:157739148	aagaaactatcatca[A/G]agtgaacaggcaacc	51429
rs863780	snp	C/T	0.499918	0.00638925	intron-variant	SNX9	GRCh38.p7	6:157739520	gtaaattagttcaac[C/T]gttgtggaagacagt	51429
rs864336	snp	G/T	0.5	0	intron-variant	SNX9	GRCh38.p7	6:157744751	tttcttcattttttt[G/T]ttttttttttttgag	51429
rs864337	snp	C/T			intron-variant	SNX9	GRCh38.p7	6:157750493	acagattaaaaactt[C/T]aatgtgaaacccaaa	51429
rs864867	snp	C/T	0.266273	0.24947	intron-variant	SNX9	GRCh38.p7	6:157733968	ACATGACAATCGTCA[C/T]CCTTGGAAAGAACAA	51429
rs912879	snp	A/G	0.368682	0.220033	intron-variant	SNX9	GRCh38.p7	6:157940867	CTACAACCCAAATCA[A/G]AACATCAATCAGTTT	51429
rs913497	snp	C/G	0.148661	0.22854	intron-variant	SNX9	GRCh38.p7	6:157823551	GAAGCGGAGTGGCCC[C/G]TCGACCACCCCTGGC	51429
rs928008	snp	C/T	0.469839	0.119042	intron-variant	SNX9	GRCh38.p7	6:157774663	TGCAGCATGGACCAA[C/T]GCAAGAGGAAATGTG	51429
rs930125	snp	C/T	0.382473	0.212016	intron-variant	SNX9	GRCh38.p7	6:157718586	AAATAAAAGCTAGAT[C/T]GGTTTGGTGTAATTC	51429
rs930126	snp	A/T	0.493477	0.0567349	intron-variant	SNX9	GRCh38.p7	6:157720223	AAACACTACATCCCT[A/T]AGAGTCGCAAATAGA	51429
rs1010833	snp	G/T			intron-variant	SNX9	GRCh38.p7	6:157798493	tattgggataattgg[G/T]gacatttgaacatgg	51429
rs1033527	snp	G/T	0.235273	0.249566	intron-variant	SNX9, LOC105378078	GRCh38.p7	6:157889887	AGCCCACAGTATGCA[G/T]TCAGTAGAGGTTATC	51429
rs1033528	snp	C/T	0.401747	0.198678	intron-variant	SNX9, LOC105378078	GRCh38.p7	6:157889758	CTATGCAGGAAAAGA[C/T]CAGACAGTTATATTT	51429
rs1034058	snp	A/G	0.448195	0.152377	intron-variant	SNX9	GRCh38.p7	6:157772693	Ctggactagtttcct[A/G]ggctgccataacaaa	51429
rs1034059	snp	C/T	0.483199	0.0901004	intron-variant	SNX9	GRCh38.p7	6:157772666	caaactaccacaaag[C/T]aggtggctttaaaac	51429
rs1043863	snp	A/G	0.270892	0.249126	utr-variant-3-prime, downstream-variant-500B	SNX9	GRCh38.p7	6:157943682	TTGTGGCTTTGGTCC[A/G]ACGGGTGAGTGGCTG	51429
rs1043864	snp	A/G	0.373598	0.21731	utr-variant-3-prime, downstream-variant-500B	SNX9	GRCh38.p7	6:157943728	TCGGGAGGGCCTGGG[A/G]GAAGGAGGGCACCCA	51429
rs1077649	snp	C/G	0.128632	0.218563	intron-variant	SNX9	GRCh38.p7	6:157940791	ACAATTAATCATCAA[C/G]CTGACCTAATCTGGT	51429
rs1095708	snp	C/G	0.499839	0.00898417	intron-variant	SNX9	GRCh38.p7	6:157736720	gtgagagagggcatc[C/G]ttgtcctgtgctggt	51429
rs1095710	snp	C/T	0.499918	0.00638925	intron-variant	SNX9	GRCh38.p7	6:157738311	aacttgctttatgaa[C/T]ctgggtgctcctgta	51429
rs1095711	snp	C/G	0.499918	0.00638925	intron-variant	SNX9	GRCh38.p7	6:157738573	tacagcacagtgatg[C/G]gtcttgactctttat	51429
rs1095712	snp	A/G	0.499839	0.00898417	intron-variant	SNX9	GRCh38.p7	6:157738739	cagcatggtacttgt[A/G]ccaaaacagatatat	51429
rs1103892	snp	C/T	0.499918	0.00638925	intron-variant	SNX9	GRCh38.p7	6:157738870	tccctatttaataaa[C/T]ggtgttgggaaaact	51429
rs1244976	snp	C/G	0	0	intron-variant	SNX9	GRCh38.p7	6:157745633	GGCATTTCCATTCTG[C/G]CCAGGGTGATTTTTC	51429
rs1328487	snp	C/T	0.00279162	0.0372561	intron-variant	SNX9	GRCh38.p7	6:157833581	CTTCAGATTCAGTGC[C/T]AGTTGTTCAGTAAGT	51429
rs1344346	snp	A/G	0.154661	0.231107	intron-variant	SNX9	GRCh38.p7	6:157772573	GCCATGCTCTCCCCA[A/G]AGGCTCTGGGGAAGG	51429
rs1359983	snp	A/C	0.0162398	0.0886349	intron-variant	SNX9	GRCh38.p7	6:157828148	GTTAGCATTTTCCAA[A/C]CATTTTAAAAGCCAT	51429
rs1359984	snp	G/T	0.409891	0.192184	intron-variant	SNX9	GRCh38.p7	6:157828079	ATTTCTATTCTAGTC[G/T]TCAAATAAAGAAGTT	51429
rs1743587	snp	A/G	0.499839	0.00898417	intron-variant	SNX9	GRCh38.p7	6:157738615	gggctaattgcccca[A/G]ttaaaagacacagac	51429
rs1743588	snp	A/G	0.318174	0.240525	intron-variant	SNX9	GRCh38.p7	6:157736953	atatgcaaatcaata[A/G]acgcaatccatcaca	51429

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