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
rs581880	snp	A/G	0	0	splice-acceptor-variant	NFX1	GRCh38.p7	9:33354085	CTTTTTTATATTTCA[A/G]AATAGCTGCAATCTC	4799
rs583428	snp	A/C	0.298398	0.245271	intron-variant	NFX1	GRCh38.p7	9:33315727	ACCAGTCTCTAACAA[A/C]AACAAAAAAAAAAAA	4799
rs583431	snp	A/C	0.298144	0.245321	intron-variant	NFX1	GRCh38.p7	9:33315730	AGTCTCTAACAACAA[A/C]AAAAAAAAAAAATTA	4799
rs587608	snp	C/G	0.306679	0.24349	intron-variant	NFX1	GRCh38.p7	9:33296725	AACTTTTTTCCCCCC[C/G]CAaaacagggtcttg	4799
rs588676	snp	C/T	0.0513262	0.151752	intron-variant	NFX1	GRCh38.p7	9:33333098	aacactttgggaggc[C/T]gaggcgggtggatca	4799
rs589212	snp	C/G	0.328382	0.237395	intron-variant	NFX1	GRCh38.p7	9:33334018	AGCTGGGATTACAGG[C/G]GTGCGCCACTGTACT	4799
rs589231	snp	C/T	0.35809	0.225425	intron-variant	NFX1	GRCh38.p7	9:33334008	ACAGGGGTGCGCCAC[C/T]GTACTTGGCTAATTT	4799
rs590132	snp	A/G	0.0517044	0.152246	intron-variant	NFX1	GRCh38.p7	9:33333789	CAAAAGTTTAAATAC[A/G]GTTTTGAGGCAGATA	4799
rs593495	snp	C/T	0.299916	0.244966	intron-variant	NFX1	GRCh38.p7	9:33317436	TTCttttctttcttt[C/T]ttttttttttttttt	4799
rs599279	snp	C/G	0.298905	0.24517	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349703	AATTGGGGGTTCTAT[C/G]CCCTGTTGTCTCTTA	4799
rs617045	snp	C/T	0.0513262	0.151752	intron-variant	NFX1	GRCh38.p7	9:33330455	CTGTTATCCTATGTA[C/T]ATTGTAATTTCTTTC	4799
rs624596	snp	A/T	0	0	intron-variant	NFX1	GRCh38.p7	9:33300061	aaaaaaaaaaatgct[A/T]taacataggtaccat	4799
rs624638	snp	A/G	0	0	intron-variant	NFX1	GRCh38.p7	9:33300033	cattttacagatgaa[A/G]aaactggcttcatgt	4799
rs626069	snp	A/G	0.4582	0.138394	intron-variant	NFX1	GRCh38.p7	9:33316108	CTTCCATCACCTATT[A/G]TGAATCCTGACCCTG	4799
rs628777	snp	C/T	0.0505692	0.150756	intron-variant	NFX1	GRCh38.p7	9:33315449	gaaaTATACTCTCTC[C/T]TTCGTCTGCCTTTCT	4799
rs636170	snp	A/G	0.49934	0.0181589	intron-variant	NFX1	GRCh38.p7	9:33330399	CAACTTTTGTAACAT[A/G]TAAATTATACTACTT	4799
rs636759	snp	A/G	0.0402882	0.136092	intron-variant	NFX1	GRCh38.p7	9:33318390	AGTGAATGGTGTTCA[A/G]CCACGGCCTTATGGA	4799
rs637628	snp	C/T	0.0166915	0.0898172	intron-variant	NFX1	GRCh38.p7	9:33338631	CCAGAAGCCCAGCAC[C/T]TGGATGAATGGAATC	4799
rs642100	snp	A/G	0.0509478	0.151255	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33351011	tagctggtcgtggtg[A/G]tacacacctgtaacc	4799
rs642157	snp	A/T	0.295599	0.245806	intron-variant	NFX1	GRCh38.p7	9:33344254	AGCAGTGAAGACAGT[A/T]ACACAGCAGGATCCT	4799
rs650325	snp	A/G	0.0402882	0.136092	intron-variant	NFX1	GRCh38.p7	9:33301853	AACTTCTGACTTCAG[A/G]TGATCCGCCTGCCTT	4799
rs662906	snp	A/G	0.0513262	0.151752	intron-variant	NFX1	GRCh38.p7	9:33346139	GATAGCCCTCCCAGC[A/G]TAGTTTGCAAGCCCC	4799
rs667602	snp	A/G	0.472147	0.114677	intron-variant	NFX1	GRCh38.p7	9:33324244	ttacaggcgtgtgcc[A/G]ccacacccagctaat	4799
rs673955	snp	A/G	0.0513262	0.151752	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353561	ATACTGAGGGATTGA[A/G]TCACCTCATCGCTTC	4799
rs675469	snp	A/G	0.441705	0.160466	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353214	CGTATTACATTGTGA[A/G]ATAAGAAGGGAAGAT	4799
rs697530	snp	A/G	0.298651	0.24522	intron-variant	NFX1	GRCh38.p7	9:33317688	aaaaTCTAGAGTCTT[A/G]ATTATggccgggcgt	4799
rs706124	snp	A/G	0.0325976	0.123435	intron-variant	NFX1	GRCh38.p7	9:33292804	ATAAGATCAGTAAAG[A/G]TGTCTAGAGAAGCCT	4799
rs706125	snp	A/G	0.0341408	0.126114	intron-variant	NFX1	GRCh38.p7	9:33292932	ATGCAGAGGGTGGCA[A/G]AGGTATTCTGGAAAC	4799
rs706126	snp	C/T	0.125874	0.217008	intron-variant	NFX1	GRCh38.p7	9:33296732	CTAAAGTAACTTTTT[C/T]CCCCCCGCAaaacag	4799
rs706127	snp	C/T	0.471578	0.115772	intron-variant	NFX1	GRCh38.p7	9:33303902	GAGGGAGACAGACAG[C/T]AAAGAAACAAAATCT	4799
rs706128	snp	A/G	0.0158815	0.0876843	intron-variant	NFX1	GRCh38.p7	9:33311102	GGATGGCAGAGACTG[A/G]AAGAGAAAGGTTTCA	4799
rs706129	snp	C/T	0.328616	0.237317	intron-variant	NFX1	GRCh38.p7	9:33317177	cccatcctggcctcc[C/T]aaagtgctgggatta	4799
rs706130	snp	C/T	0.49934	0.0181589	intron-variant	NFX1	GRCh38.p7	9:33330430	TCTTTCAGGAAAAAA[C/T]CCATATATGATTACA	4799
rs706133	snp	C/T	0.298905	0.24517	intron-variant	NFX1	GRCh38.p7	9:33343051	ATCTCAGGATCACTG[C/T]TCATATCCCAAGTTT	4799
rs706134	snp	C/T	0.496382	0.0423778	intron-variant	NFX1	GRCh38.p7	9:33345618	GTAGGATCCCACTTT[C/T]ACATTGGGGAAAAAA	4799
rs830575	snp	A/G	0.29432	0.24604	intron-variant	NFX1	GRCh38.p7	9:33291522	CCCCAACGGCTGGTC[A/G]GGGACAGAGCTGAGA	4799
rs830576	snp	C/T	0.272117	0.249026	utr-variant-5-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33290534	AGCTGTACAGCCAAG[C/T]CAGCACTGTCACCAG	4799
rs830577	snp	A/C	0.294576	0.245994	upstream-variant-2KB	NFX1	GRCh38.p7	9:33288612	AGAGAGGAATGGTAA[A/C]AGAGAAAATTCTGCA	4799
rs830578	snp	A/G	0.32885	0.23724	intron-variant	NFX1	GRCh38.p7	9:33337651	acctcgaattcctgc[A/G]ctcaaatgagcctcc	4799
rs830579	snp	C/T	0	0	intron-variant	NFX1	GRCh38.p7	9:33325521	gcccgccaccatgcc[C/T]ggctaattttttgta	4799
rs830580	snp	C/G	0	0	intron-variant	NFX1	GRCh38.p7	9:33325468	caccgtgttagccag[C/G]atggtctcgatctcc	4799
rs831264	snp	C/T	0.468249	0.121932	intron-variant	NFX1	GRCh38.p7	9:33362623	tctcctcaacctccc[C/T]tttccaccctgtccc	4799
rs831265	snp	A/T	0.298651	0.24522	intron-variant	NFX1	GRCh38.p7	9:33362101	tgggtctggctcttg[A/T]tgcccaggctggagt	4799
rs831266	snp	A/G	0.32955	0.237006	intron-variant	NFX1	GRCh38.p7	9:33359577	gagtcttgctgtatc[A/G]tctaggctagagtgt	4799
rs831267	snp	A/C	0.465263	0.127129	intron-variant	NFX1	GRCh38.p7	9:33334835	TCCTGCttattaata[A/C]tggggaaaaactgga	4799
rs831277	snp	A/T	0.29789	0.24537	intron-variant	NFX1	GRCh38.p7	9:33314975	TTCACAATTAAAAAA[A/T]TTTTTTCTATTCATG	4799
rs831287	snp	A/G	0.320335	0.239902	intron-variant	NFX1	GRCh38.p7	9:33294093	GCTAACAGTTCAGGG[A/G]TATCAATCATCAGGT	4799
rs831288	snp	C/G	0.0325976	0.123435	intron-variant	NFX1	GRCh38.p7	9:33293885	TTATTTCAACGGTTA[C/G]TGAGAAATTTAAATA	4799
rs844216	snp	C/T	0.298398	0.245271	intron-variant	NFX1	GRCh38.p7	9:33336717	gctatttgggaggct[C/T]gtgtgggaggaccac	4799
rs844217	snp	A/G	0	0	intron-variant	NFX1	GRCh38.p7	9:33325479	agacagggtttcacc[A/G]tgttagccagcatgg	4799
rs844238	snp	A/T	0.0345262	0.126772	intron-variant	NFX1	GRCh38.p7	9:33362630	accaacctctcctca[A/T]cctcccttttccacc	4799
rs854169	snp	A/G	0	0	intron-variant	NFX1	GRCh38.p7	9:33355829	tttgtatttttagta[A/G]aaatggggtttcacc	4799
rs854170	snp	A/G	0	0	intron-variant	NFX1	GRCh38.p7	9:33355947	accacgcccagccca[A/G]aacattcttaaactt	4799
rs863816	snp	A/G	0	0	intron-variant	NFX1	GRCh38.p7	9:33325401	gctgggattacaggc[A/G]tgagccaccgcgccc	4799
rs1070046	snp	A/C	0.0402882	0.136092	intron-variant	NFX1	GRCh38.p7	9:33323668	tgaggcaggagaatc[A/C]cttgaacccaggagg	4799
rs1070047	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33323492	aggcatggtggctca[C/T]gcctgtaatcccagc	4799
rs1096495	snp	C/T	0.465158	0.127307	intron-variant	NFX1	GRCh38.p7	9:33334218	ATCCCCCAGCCCTGG[C/T]CTCCCAAAGCATAAG	4799
rs1103478	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33326392	cacttcagcctgggc[A/G]acagagcaagcctct	4799
rs1198239	snp	A/G	0.313082	0.241911	intron-variant	NFX1	GRCh38.p7	9:33358135	tctgtctcaaaaaaa[A/G]aaTTACaagtaatac	4799
rs1198251	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33357007	catgcccggctTAtt[A/T]ttttttttttttttt	4799
rs1702623	snp	C/G	0	0	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351867	GAACTGTCTACAGTG[C/G]CCCCTGGGCATGCAT	4799
rs1702963	snp	A/G	0.295854	0.245759	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289508	CACCCCCTGCCCGAC[A/G]CTTCTCCCCACCCCC	4799
rs1971352	snp	A/G	0.124144	0.21601	intron-variant	NFX1	GRCh38.p7	9:33318104	TATTTTATTTTTATT[A/G]TATATGTGATTTTAA	4799
rs2230122	snp	A/G	0.134544	0.221743	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33369945	GAAAATAACCAAGGA[A/G]CCAATAATTGACTAT	4799
rs2274866	snp	G/T	0.00161325	0.0283553	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33367586	TGATGAGGAATCGGT[G/T]GTGGAGGCCGTGCCT	4799
rs2292243	snp	C/T	0.207559	0.246371	intron-variant	NFX1	GRCh38.p7	9:33328814	TGCCTTATCCCACTA[C/T]AGGCCTCTGGACCTT	4799
rs2485447	snp	G/T	0	0	intron-variant	NFX1	GRCh38.p7	9:33290603	CCTGTCTCAGGTATT[G/T]TCCCGGCCCGAGCGG	4799
rs2661052	snp	A/G	0.472241	0.114494	intron-variant	NFX1	GRCh38.p7	9:33301851	CTTCTGACTTCAGAT[A/G]ATCCGCCTGCCTTGG	4799
rs2860036	snp	A/G	0.0141037	0.0827824	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33344122	GCCTAGTACCACAGG[A/G]AACTGGAGGGTAAAT	4799
rs2940425	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33307800	AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA	4799
rs2993125	snp	C/T	0.0509478	0.151255	intron-variant	NFX1	GRCh38.p7	9:33308072	AGCCTCCCAACATGC[C/T]AGGATTACTGGTGTG	4799
rs3739676	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33346871	TTGCTTTATGTTAAA[A/G]TGTTGAAGGACAAGC	4799
rs3814515	snp	C/T	0.0991586	0.199366	intron-variant	NFX1	GRCh38.p7	9:33290659	GAGGCCCTAGAACTT[C/T]GTCACTGACCCAATT	4799
rs3849903	snp	A/G	0.49334	0.057322	intron-variant	NFX1	GRCh38.p7	9:33318590	TGCATAGGTCTGATC[A/G]GTACTCTATTTGGCC	4799
rs3942770	snp	A/C	0	0	intron-variant	NFX1	GRCh38.p7	9:33327989	TAAATCTTCTTTTTC[A/C]TCAGGCCCCACATCT	4799
rs4008680	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33363301	attattattattatt[A/T]ttagacagagtctca	4799
rs4878532	snp	C/T	0.313082	0.241911	intron-variant	NFX1	GRCh38.p7	9:33312688	CCAGGTGGGCCAACA[C/T]GGTGAAACCCCGTCT	4799
rs4878533	snp	C/T	0.0119091	0.0762411	intron-variant	NFX1	GRCh38.p7	9:33354594	ATAACAGAGAGGCCA[C/T]CATCCCACCTGTCCT	4799
rs4878534	snp	A/G	0.115383	0.210662	intron-variant	NFX1	GRCh38.p7	9:33354939	TTGCCCTTGAGCTCT[A/G]TGAAATTAATGGGAG	4799
rs4879682	snp	C/G	0.492823	0.0594727	intron-variant	NFX1	GRCh38.p7	9:33290690	AGCCACTCATATCGC[C/G]AGAGTAGCACATGCT	4799
rs4879683	snp	A/G	0.0279526	0.114869	intron-variant	NFX1	GRCh38.p7	9:33315974	TATTGTTCGAAACTC[A/G]GTGTTCTTTGAGTAC	4799
rs4879685	snp	A/G	0.493154	0.0581045	intron-variant	NFX1	GRCh38.p7	9:33335112	TGAAATTCACATAAC[A/G]TAATTAACCATTTTA	4799
rs4879686	snp	G/T	0.493837	0.055168	intron-variant	NFX1	GRCh38.p7	9:33343399	GAATAGCGGATACTT[G/T]GTTTAATAGAAGGTA	4799
rs4879688	snp	C/T	0.0970103	0.197722	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366400	CCCTTTGTCCCTAAC[C/T]CTGTCCAGCTGCGAC	4799
rs5017299	snp	C/T			missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33342821	TGTGAAGAACCTTGT[C/T]ATCGTGGAAACTGCC	4799
rs5897541	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33304853	TAGGACAATACCAAT[-/T]ACTTAATACCTTATT	4799
rs5897542	in-del	-/A	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33317973	GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	4799
rs7019355	snp	A/G	0.100231	0.200173	intron-variant	NFX1	GRCh38.p7	9:33298111	gaagacaggcagaaa[A/G]cacttagatatttaa	4799
rs7024137	snp	C/T	0.0984431	0.198823	intron-variant	NFX1	GRCh38.p7	9:33318169	GATCATTAGATCTTA[C/T]ACTCTCATGCCAATT	4799
rs7027207	snp	G/T	0.0152369	0.0859434	intron-variant	NFX1	GRCh38.p7	9:33354238	TCAATTAGACTTCAA[G/T]TAGAGGGCAGAGATT	4799
rs7033115	snp	A/G	0.0042729	0.0460238	intron-variant	NFX1	GRCh38.p7	9:33294400	TCTCTTTACTGGCAT[A/G]TCTATTTTTTATGTC	4799
rs7037491	snp	C/T	0.0126979	0.078662	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353304	CTAAGCTCTGTGCTC[C/T]TCTGGTGTGAGGGTT	4799
rs7038216	snp	A/G	0.0479149	0.147179	intron-variant	NFX1	GRCh38.p7	9:33353719	ttgaaatggagtttc[A/G]ctcctgttgcccagg	4799
rs7039578	snp	C/T	0.0138799	0.0821421	intron-variant	NFX1	GRCh38.p7	9:33311621	gcagtggtgcgatct[C/T]ggctcactgcaacct	4799
rs7040601	snp	C/T	0.0980852	0.198549	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350217	GCTGAGGTAGGAGAA[C/T]CGCTTGAACCCAGGA	4799
rs7046204	snp	A/G	0.0444908	0.142359	upstream-variant-2KB	NFX1	GRCh38.p7	9:33290264	actgcactcaagcct[A/G]ggtaaggcagcaaga	4799
rs7048066	snp	G/T	0.0256215	0.110247	intron-variant	NFX1	GRCh38.p7	9:33334427	tgccattgcactcta[G/T]cctggtgacagagcg	4799
rs7848862	snp	A/G/T	0.0134861	0.0810011	intron-variant	NFX1	GRCh38.p7	9:33310597	CTAGCATGCCTCCCC[A/G/T]CATGTCAGCCTTCTT	4799
rs7866990	snp	C/T	0.0988009	0.199095	intron-variant	NFX1	GRCh38.p7	9:33301100	CTGCCCCTTTTTGGC[C/T]TCAGTCTGAATAGCC	4799
rs7867024	snp	C/G/T	0.0479149	0.147179	intron-variant	NFX1	GRCh38.p7	9:33311840	acaggcatgagctac[C/G/T]gcgctcggtcGGCAA	4799

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