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
rs339808	snp	A/T	0.0479149	0.147179	intron-variant	SPAG16	GRCh38.p7	2:213425003	CTCTTACTTTGAGTA[A/T]ATCCCTTATTCCTGA	79582
rs339809	snp	A/G	0.0535932	0.154675	intron-variant	SPAG16	GRCh38.p7	2:213411043	ttcaagagcttatca[A/G]tcagttagcccttgt	79582
rs339810	snp	C/T	0.0267878	0.112589	intron-variant	SPAG16	GRCh38.p7	2:213413897	TTTTTTGGGATATTT[C/T]ACAGTGCAAACAAAG	79582
rs339811	snp	A/G	0.046775	0.145601	intron-variant	SPAG16	GRCh38.p7	2:213418905	TTAGGGGCACCATCA[A/G]CTATACAAATTACTG	79582
rs339812	snp	G/T	0.0479149	0.147179	intron-variant	SPAG16	GRCh38.p7	2:213419689	TTTTTTCTTTGAAAA[G/T]AATTCACATTACATG	79582
rs339813	snp	A/C	0.046775	0.145601	intron-variant	SPAG16	GRCh38.p7	2:213390088	tcctcaagcttcatc[A/C]atgttgtggaatttg	79582
rs339814	snp	A/G	0.000399281	0.0141238	intron-variant	SPAG16	GRCh38.p7	2:213394145	CTGATCTTGAGATAA[A/G]AAAGGGTTTCTTAAT	79582
rs339815	snp	A/G	0.499971	0.00379382	intron-variant, utr-variant-3-prime, downstream-variant-500B	SPAG16	GRCh38.p7	2:213396810	gactgtaaagaacac[A/G]gataaagggtatgGG	79582
rs339816	snp	G/T	0.046775	0.145601	intron-variant, utr-variant-3-prime	SPAG16	GRCh38.p7	2:213397597	ttcagagagttagaa[G/T]gatcatccatatcaa	79582
rs339817	snp	A/C/G/T	0.0456336	0.143994	intron-variant, utr-variant-3-prime	SPAG16	GRCh38.p7	2:213399109	gaaatacaaataaaa[A/C/G/T]tttttagaattgaaa	79582
rs339818	snp	C/T	0.0263992	0.111815	intron-variant, utr-variant-3-prime	SPAG16	GRCh38.p7	2:213399906	agtaaatttaaaact[C/T]agatgaaatggtcat	79582
rs339819	snp	A/G	0.046775	0.145601	intron-variant, utr-variant-3-prime	SPAG16	GRCh38.p7	2:213400339	aacaaaaattaaaat[A/G]ctacatataaacatc	79582
rs339820	snp	A/G	0.0479149	0.147179	intron-variant	SPAG16	GRCh38.p7	2:213430283	tcttttgaattaatc[A/G]agtcagacaaaagtg	79582
rs339821	snp	C/T	0.47934	0.0995154	intron-variant	SPAG16	GRCh38.p7	2:213433689	aggaattgtattaaa[C/T]ctgtagattgctttg	79582
rs339822	snp	A/C	0.35445	0.227135	intron-variant	SPAG16	GRCh38.p7	2:213433944	gacaagaacgagaca[A/C]tgtctcaaaaaaaaa	79582
rs339823	snp	A/G	0.0448719	0.142907	intron-variant	SPAG16	GRCh38.p7	2:213434263	tatccttctgcatcc[A/G]gctatccaattttcc	79582
rs339824	snp	C/G	0.256619	0.249912	intron-variant	SPAG16	GRCh38.p7	2:213434307	cttgagttgattttt[C/G]tatatgctgagagat	79582
rs339825	snp	G/T	0.0479149	0.147179	intron-variant	SPAG16	GRCh38.p7	2:213436163	AAAATGTGATTAAAT[G/T]ATTTAACATTAAACA	79582
rs714126	snp	C/T	0.484841	0.0857308	intron-variant	SPAG16	GRCh38.p7	2:213902193	CTTTATTCTTTGGTA[C/T]ATCCACAGAAAATAA	79582
rs714567	snp	G/T	0.130008	0.219321	intron-variant	SPAG16	GRCh38.p7	2:213767816	TGTGACATTTATTGG[G/T]CAACAAATGAGCCTG	79582
rs716992	snp	C/G			intron-variant	SPAG16	GRCh38.p7	2:213768793	gcctataaggcataa[C/G]aaatgtatgtcaata	79582
rs720015	snp	C/T	0.479824	0.098392	intron-variant	SPAG16	GRCh38.p7	2:213877347	CAAGGTCTCACTTTG[C/T]TGTGTAGTCAGGAGT	79582
rs720016	snp	A/G	0.479824	0.098392	intron-variant	SPAG16	GRCh38.p7	2:213877472	ACGCTACCACACCCA[A/G]CTAATTAAAAAATCA	79582
rs721759	snp	C/T	0.0825414	0.185628	intron-variant	SPAG16	GRCh38.p7	2:214053307	TTAATTTTCATTTTT[C/T]TTTGTTCTAGTTAAG	79582
rs723621	snp	C/T	0.0103295	0.0711199	intron-variant, utr-variant-5-prime	SPAG16	GRCh38.p7	2:213300561	AAATGCAGAAAAAAA[C/T]ATGGGGATCTAGCTG	79582
rs723622	snp	A/G	0.0652144	0.168387	intron-variant, utr-variant-5-prime	SPAG16	GRCh38.p7	2:213300694	aattctgtctatgtt[A/G]tctgtgtagaagttt	79582
rs724953	snp	A/G	0	0	intron-variant	SPAG16	GRCh38.p7	2:213735421	AATTTATATTACTGA[A/G]AAATACTCTTCTATA	79582
rs724954	snp	C/T	0.474363	0.110278	intron-variant	SPAG16	GRCh38.p7	2:213735568	ttcccttatcttgtc[C/T]tgactaatggctgga	79582
rs727502	snp	A/G	0.480382	0.097079	intron-variant	SPAG16	GRCh38.p7	2:213715266	TCTATCTATCTATCT[A/G]TCCATTCATCCATCT	79582
rs727503	snp	C/T	0.491157	0.065903	intron-variant	SPAG16	GRCh38.p7	2:213715585	CTTCCTCATGGTATA[C/T]ATTGAGTGAATTACG	79582
rs737690	snp	C/T	0.311369	0.242351	intron-variant	SPAG16	GRCh38.p7	2:214043190	CTCATGCAGTGGGAA[C/T]ATTTAAATTATGAAA	79582
rs759776	snp	C/T	0.483418	0.0895317	intron-variant	SPAG16	GRCh38.p7	2:214115986	GATTCAGGTAGGAGG[C/T]TGCAGAGCCCCAGTG	79582
rs759777	snp	C/T	0.280256	0.248162	intron-variant	SPAG16	GRCh38.p7	2:214042615	ATAAAGATAGTTCAA[C/T]GTTTCCTAAGATTGA	79582
rs766258	snp	A/G	0.211212	0.246973	intron-variant	SPAG16	GRCh38.p7	2:213312256	GTTCTATGAACCACT[A/G]AAAAGTTTCCATTGC	79582
rs766605	snp	C/T	0.214843	0.247516	intron-variant	SPAG16	GRCh38.p7	2:214120679	GAAATAAAATATCCA[C/T]AGGCACCGCTTCTCA	79582
rs769348	snp	C/G	0.490007	0.0699769	intron-variant	SPAG16	GRCh38.p7	2:214079844	TTGAAATTCTCTTTT[C/G]TCTTCTAAACAAGGA	79582
rs769349	snp	A/T	0.0329836	0.124112	intron-variant	SPAG16	GRCh38.p7	2:214079843	TGAAATTCTCTTTTC[A/T]CTTCTAAACAAGGAC	79582
rs878923	snp	A/G	0.326035	0.238157	intron-variant	SPAG16	GRCh38.p7	2:213725643	agaagagggtgcggc[A/G]tgtcttagcaacagt	79582
rs889887	snp	A/G	0.0490535	0.14873	intron-variant	SPAG16	GRCh38.p7	2:213607726	CTTAGATGTATTTTA[A/G]AATGCACATGAGTGG	79582
rs901950	snp	A/C/G	0	0	intron-variant	SPAG16	GRCh38.p7	2:213377881	GAACTAATAGGATGT[A/C/G]TATATATATATATAT	79582
rs905537	snp	C/T	0.173643	0.238054	intron-variant	SPAG16	GRCh38.p7	2:213522440	TTCCCTCTGCCCAGT[C/T]CTCTCTTCCCACCCC	79582
rs907122	snp	A/T	0.466721	0.124627	intron-variant	SPAG16	GRCh38.p7	2:213932730	TTCCTCACCAAAAAG[A/T]TGGATCACTGTGAAG	79582
rs907123	snp	C/G	0.120674	0.21395	intron-variant	SPAG16	GRCh38.p7	2:213932827	CAATTATCTATGACA[C/G]TCAGTCTGAATAATT	79582
rs918327	snp	A/G	0.0810805	0.184299	intron-variant	SPAG16	GRCh38.p7	2:214067355	TATCAAACATTGTGT[A/G]GCACACAATAGAAAT	79582
rs918352	snp	A/G	0.499477	0.0161657	intron-variant	SPAG16	GRCh38.p7	2:214220213	AACACATTTTTAGAA[A/G]GTCTTGAATCCTTGG	79582
rs918353	snp	C/T	0.172028	0.23753	intron-variant	SPAG16	GRCh38.p7	2:214248101	AAACACAAAATAGAG[C/T]AATCTCTAGTTCAGA	79582
rs918354	snp	A/T	0.176219	0.238865	intron-variant	SPAG16	GRCh38.p7	2:214251131	CCTATGATAAGTTAC[A/T]ATGTATATTGTAACA	79582
rs918355	snp	C/T	0.26818	0.249338	intron-variant	SPAG16	GRCh38.p7	2:214260208	TGATAAAAGACTATA[C/T]ATTGGGTACAGTATA	79582
rs918839	snp	C/T	0.362104	0.223456	intron-variant	SPAG16	GRCh38.p7	2:213606891	TCTCATAATATTCTG[C/T]AGATTATTCGCCATT	79582
rs925356	snp	A/G	0.401747	0.198678	intron-variant	SPAG16	GRCh38.p7	2:213933681	CAGAGGGACTTGCAA[A/G]ATTCAACAGCTTCTT	79582
rs925357	snp	C/T	0.437965	0.164831	intron-variant	SPAG16	GRCh38.p7	2:213978789	CAACAGTCACAGGAC[C/T]GAGCTTGAAAACAGA	79582
rs929725	snp	C/T	0.348794	0.229651	intron-variant	SPAG16	GRCh38.p7	2:214158335	CATTCCACTTTTCCT[C/T]GATCCAAAACAGAAA	79582
rs931993	snp	A/G	0.391769	0.205917	intron-variant	SPAG16	GRCh38.p7	2:213967645	TCATAGCAGGGGTTA[A/G]GACATAATTTTCATC	79582
rs933978	snp	C/T	0.331874	0.236213	intron-variant	SPAG16	GRCh38.p7	2:213849783	TTATTATATTAATGA[C/T]AGAGAGTAGATTCTT	79582
rs933979	snp	C/G	0.140242	0.224618	intron-variant	SPAG16	GRCh38.p7	2:213725333	tgagccAACTCTCTG[C/G]TCTTTGTTATTCAAT	79582
rs933980	snp	A/G	0.140242	0.224618	intron-variant	SPAG16	GRCh38.p7	2:213725432	TAAATTCATCATCAT[A/G]GAATGCCCATCCATC	79582
rs933981	snp	G/T	0.140242	0.224618	intron-variant	SPAG16	GRCh38.p7	2:213725526	ttccaacaaaggact[G/T]ccccatagcatccca	79582
rs933982	snp	C/T	0.130008	0.219321	intron-variant	SPAG16	GRCh38.p7	2:213726350	GGATTGATTCCTACC[C/T]TTCATTAGGTACCTT	79582
rs951866	snp	A/G	0.405429	0.195811	intron-variant	SPAG16	GRCh38.p7	2:213945976	TAAAAATATAACAAT[A/G]CTACATTTATATTTG	79582
rs953133	snp	C/T	0.498945	0.022939	intron-variant	SPAG16	GRCh38.p7	2:213941351	TGGAGATTTATAACT[C/T]GTAATGAATGTTAAG	79582
rs953134	snp	A/T	0.270892	0.249126	intron-variant	SPAG16	GRCh38.p7	2:213941413	ATAATTTATTTTAGA[A/T]TTTTGCATACATATA	79582
rs953881	snp	C/T	0.362104	0.223456	intron-variant	SPAG16	GRCh38.p7	2:213662571	TGGCTAAATATGTCA[C/T]ATTATATTCCTATTA	79582
rs956179	snp	C/T	0.496483	0.0417852	intron-variant	SPAG16	GRCh38.p7	2:214053273	ATTTAATATAGATTC[C/T]AAATTTCTCCTCTTA	79582
rs965421	snp	A/G	0.482831	0.0910472	intron-variant	SPAG16	GRCh38.p7	2:214263303	TCATCTGTCCTCTCC[A/G]GTGAATTCTTAATTA	79582
rs974176	snp	C/T	0.478354	0.101757	intron-variant	SPAG16	GRCh38.p7	2:214304188	TGTAAAGGACATAAT[C/T]TTGTTCTTTGTTATT	79582
rs975956	snp	C/T	0.370795	0.21888	intron-variant, nc-transcript-variant, utr-variant-5-prime	SPAG16	GRCh38.p7	2:213297049	GCCCACAAACTAATC[C/T]TGAATTTATTAGAAG	79582
rs976911	snp	A/G	0	0	intron-variant	SPAG16	GRCh38.p7	2:214245415	TCCTGTATCTTAATG[A/G]TACATTTTTATAATT	79582
rs977251	snp	C/T	0.192401	0.243274	intron-variant	SPAG16	GRCh38.p7	2:213319976	AATAGAACTTAAAAT[C/T]TAAAAAATTAGACAA	79582
rs977252	snp	G/T	0.0460142	0.144533	intron-variant	SPAG16	GRCh38.p7	2:213320174	CATTCTTAGAAAATG[G/T]AGAATGAAGTTTTGT	79582
rs1012556	snp	G/T	0.211516	0.24702	intron-variant	SPAG16	GRCh38.p7	2:213324867	gagcaactggaattc[G/T]catgtattcctactg	79582
rs1012557	snp	A/T	0.211212	0.246973	intron-variant	SPAG16	GRCh38.p7	2:213324687	ttcacagcagtttta[A/T]ctttaataaccaact	79582
rs1014450	snp	C/T	0.404559	0.196498	intron-variant	SPAG16	GRCh38.p7	2:214130069	ggggtctggcttcaa[C/T]agagaaaattctcac	79582
rs1014451	snp	A/G	0.301681	0.2446	intron-variant	SPAG16	GRCh38.p7	2:214130174	aagccctgattggCA[A/G]GCTTCCAAGCCCCAA	79582
rs1014452	snp	A/G	0.301681	0.2446	intron-variant	SPAG16	GRCh38.p7	2:214130193	TCCAAGCCCCAAACT[A/G]GAAGTCTCTAGCAGC	79582
rs1015355	snp	A/G	0.24449	0.249939	intron-variant	SPAG16	GRCh38.p7	2:214129356	tggctgacttcattc[A/G]ttttcatctcttgat	79582
rs1015970	snp	C/G	0.387263	0.208947	intron-variant	SPAG16	GRCh38.p7	2:214023755	CCTTTGCATACACAT[C/G]ACAAATATCATTCCT	79582
rs1015971	snp	G/T	0.0329836	0.124112	intron-variant	SPAG16	GRCh38.p7	2:214067952	GTTACTTTGTAAATA[G/T]AATTCAAATTAGAAT	79582
rs1017194	snp	C/T	0.243347	0.249911	intron-variant	SPAG16	GRCh38.p7	2:214222478	AAATGAACCAGCCAC[C/T]TACACAAACTCTTGT	79582
rs1021310	snp	C/T	0.194278	0.243711	intron-variant, upstream-variant-2KB	SPAG16	GRCh38.p7	2:213295337	AATTAGAGTAACTTA[C/T]AGTTTTTGAAAGTCT	79582
rs1023605	snp	A/G	0.461923	0.132621	intron-variant	SPAG16	GRCh38.p7	2:214193425	tgtgtgtgtgtgtgt[A/G]tgagagagagagaga	79582
rs1023606	snp	A/T			intron-variant	SPAG16	GRCh38.p7	2:214193432	gtgtgtgtatgagag[A/T]gagagagagagagag	79582
rs1023607	snp	A/T	0.392881	0.205147	intron-variant	SPAG16	GRCh38.p7	2:214193707	TCACTAAATGATGGT[A/T]CCTATTTTATATTCA	79582
rs1023608	snp	C/T	0.393065	0.205018	intron-variant	SPAG16	GRCh38.p7	2:214193708	CACTAAATGATGGTT[C/T]CTATTTTATATTCAG	79582
rs1023609	snp	A/G	0.499937	0.0055907	intron-variant	SPAG16	GRCh38.p7	2:214230416	CAGCTCTGGCTGTGC[A/G]CAAATTCTTTTTGCA	79582
rs1024928	snp	A/G	0.498392	0.028309	intron-variant	SPAG16	GRCh38.p7	2:214128875	tgttaggtgggaaag[A/G]agcagtgctcaaact	79582
rs1027939	snp	C/T	0.373196	0.217538	intron-variant	SPAG16	GRCh38.p7	2:213937862	TAAACTTGATGTGAA[C/T]GTTCTTTGATACCAA	79582
rs1027940	snp	A/C	0.434398	0.168811	intron-variant	SPAG16	GRCh38.p7	2:213937912	AAAAAGGTAAATGTC[A/C]TTAGGATTTTAAAAT	79582
rs1027941	snp	C/T	0.384785	0.210554	intron-variant	SPAG16	GRCh38.p7	2:213937945	ATCCCTATTCCTTTC[C/T]ACAGCAAATGCTATT	79582
rs1028137	snp	C/G	0.344592	0.231414	intron-variant	SPAG16	GRCh38.p7	2:213670816	ATATGCGGCATTTGA[C/G]AAATTCAAAAACTAA	79582
rs1030143	snp	A/G	0.227074	0.248947	intron-variant	SPAG16	GRCh38.p7	2:214077175	AAATATTTATTAATA[A/G]TAACAGGCAACCACA	79582
rs1030288	snp	C/T	0.132066	0.220435	intron-variant	SPAG16	GRCh38.p7	2:213451701	tttatataaatgggc[C/T]agtgaggagggtgtg	79582
rs1033065	snp	G/T	0.480931	0.0957637	intron-variant	SPAG16	GRCh38.p7	2:213897772	CCATAGCCAGTAATT[G/T]AGTCCTTACTTAGAG	79582
rs1033066	snp	A/G	0.0539704	0.155153	intron-variant	SPAG16	GRCh38.p7	2:213897979	TGACAATTTTTAAAA[A/G]ACTATTATATGAAGA	79582
rs1033067	snp	C/T	0.484841	0.0857308	intron-variant	SPAG16	GRCh38.p7	2:213900369	ACCAATATCTCGGAA[C/T]GACTGTGATTATACA	79582
rs1033068	snp	A/C	0.484841	0.0857308	intron-variant	SPAG16	GRCh38.p7	2:213900391	GATTATACAAAACAC[A/C]GATATTAAAATAATT	79582
rs1033069	snp	A/G	0.484841	0.0857308	intron-variant	SPAG16	GRCh38.p7	2:213900484	TGTCCTCTCCCTGCA[A/G]CAAACCGGGTCTTCA	79582
rs1033070	snp	C/T	0.495634	0.0465208	intron-variant	SPAG16	GRCh38.p7	2:214016024	GGAGGAGGAGGAGTT[C/T]AGGGTGAGAAACTTT	79582
rs1038662	snp	C/T	0.046775	0.145601	intron-variant	SPAG16	GRCh38.p7	2:213324340	gagtttatccgtttg[C/T]caaaattATATAGCT	79582
rs1039500	snp	C/T			intron-variant	SPAG16	GRCh38.p7	2:213540704	AACATTCTCCAACTT[C/T]TCCAAATTGTGAAGA	79582
rs1039502	snp	A/C	0.0240643	0.107019	intron-variant	SPAG16	GRCh38.p7	2:213497122	CTGTAAAACTAGCAG[A/C]CTGTATCtttatatt	79582

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