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
rs6583	snp	C/T	0.460252	0.135255	utr-variant-3-prime, upstream-variant-2KB	SPATA13, C1QTNF9	GRCh38.p7	13:24307046	ATGAATTTTAATATA[C/T]AAAACAACAAATATA	221178
rs715921	snp	C/T	0.425894	0.177655	intron-variant	SPATA13	GRCh38.p7	13:24221351	AATAACCATAAAAGA[C/T]TACCAACTTTTAAGT	221178
rs724932	snp	A/T	0.378372	0.214524	intron-variant	SPATA13	GRCh38.p7	13:23995972	CTATCTGCTCGGTTG[A/T]CTCTCTAGCTCTTCA	221178
rs727113	snp	C/T	0.364401	0.222289	intron-variant	SPATA13	GRCh38.p7	13:24112702	GACTGAGAAAGTAGA[C/T]GAAGACTGAGACATC	221178
rs728096	snp	C/G	0	0	intron-variant	SPATA13	GRCh38.p7	13:24220291	TTCTTGGTTATAAAA[C/G]GTCTTATAGTGCCCT	221178
rs728097	snp	C/G/T	0.552443	0.192851	intron-variant	SPATA13	GRCh38.p7	13:24220247	GCACCAAGGTTAGGC[C/G/T]GATTCCCATGTCTTG	221178
rs736081	snp	C/T	0.499885	0.00758699	intron-variant	SPATA13	GRCh38.p7	13:24085587	TCCAGAGGAAGGTGC[C/T]CCTTCTGCCACCACG	221178
rs737529	snp	A/G	0.491263	0.0655142	intron-variant	SPATA13	GRCh38.p7	13:24133973	TGAGGAGGGGGCTGG[A/G]TCGAGCCCCTGGGGG	221178
rs745918	snp	A/G	0.495483	0.0473088	intron-variant	SPATA13	GRCh38.p7	13:24083274	GTCCTCTTGCAGGCC[A/G]TGAGTGACACCAGCT	221178
rs745919	snp	C/T	0.482831	0.0910472	intron-variant	SPATA13	GRCh38.p7	13:24083330	CACCAAACCCTGCCC[C/T]GCCCACAGGAGTCCA	221178
rs746798	snp	A/G	0.459687	0.136129	intron-variant	SPATA13	GRCh38.p7	13:24040259	CACTGAGTGCTCTCT[A/G]TGCATCCAGCTCTGG	221178
rs747310	snp	C/T	0.488606	0.0746142	intron-variant	SPATA13	GRCh38.p7	13:24134525	CATTTCCCATTGGGA[C/T]GCTTTGCTAATCCAG	221178
rs747311	snp	A/T	0.0584853	0.160693	intron-variant	SPATA13	GRCh38.p7	13:24134486	TAAGCTGCCAAAAAG[A/T]GATGTGCTGCTCTCG	221178
rs754134	snp	A/G	0.499203	0.0199521	intron-variant	SPATA13	GRCh38.p7	13:23990616	TAGTGGATTCTTCTC[A/G]GATCCAGCATGTCCC	221178
rs754135	snp	A/G	0.499053	0.0217445	intron-variant	SPATA13	GRCh38.p7	13:23990651	CTTGCAAATTGCCCT[A/G]TGCTATAATTGTCTA	221178
rs756025	snp	C/T	0.325799	0.238232	intron-variant	SPATA13	GRCh38.p7	13:24094381	CCTACAATGTTGATC[C/T]GTTTTTCACAACCCT	221178
rs756026	snp	A/G	0.481087	0.0953875	intron-variant	SPATA13	GRCh38.p7	13:24094259	CATTTGTGAGGCCAC[A/G]ATGTTCTCGCCAAAG	221178
rs871970	snp	C/T	0.489492	0.0717183	intron-variant	SPATA13	GRCh38.p7	13:24050398	TTATAACAAGGATAT[C/T]TGATTTCTTGTGAGG	221178
rs872196	snp	C/T	0.309154	0.242901	intron-variant	SPATA13	GRCh38.p7	13:23992598	TCATCATACATGGGA[C/T]TACCCCTGCCAACAT	221178
rs873868	snp	A/G	0.306927	0.243432	intron-variant	SPATA13	GRCh38.p7	13:23991320	CTACATTCTGCAAAC[A/G]CAGGATTTATTGCCC	221178
rs877039	snp	C/T	0.250732	0.249999	intron-variant	SPATA13	GRCh38.p7	13:24078588	GTCCCAGCATGGTGC[C/T]GACAGCAGCAGGCCT	221178
rs880357	snp	C/T	0	0	intron-variant, upstream-variant-2KB	SPATA13, SPATA13-AS1	GRCh38.p7	13:24255497	tggtcatctgaatgg[C/T]ttgacctgtgaaatc	221178
rs881428	snp	C/T	0.490782	0.0672626	intron-variant	SPATA13	GRCh38.p7	13:24236041	gtgacagtccttgaa[C/T]ttttccaagcctcag	221178
rs882554	snp	A/G	0.270621	0.249148	intron-variant	SPATA13	GRCh38.p7	13:24011704	ACTAGTTAAGCAGGA[A/G]CCTGGGAGTCTCCAA	221178
rs883262	snp	C/T	0.499767	0.0107802	intron-variant	SPATA13	GRCh38.p7	13:24024473	TCTTCTTGCATGTGG[C/T]TGGTCTTGTCACTAG	221178
rs883645	snp	A/G	0.0652144	0.168387	intron-variant	SPATA13	GRCh38.p7	13:24058060	GCAAGATGAGCTCCC[A/G]TCTGGCCATGCTGTG	221178
rs883646	snp	C/G	0.0704125	0.17392	intron-variant	SPATA13	GRCh38.p7	13:24058256	TTGAAAACTCTCTAC[C/G]TGATATTGTTATCTG	221178
rs912136	snp	C/G	0.5	0.00019968	intron-variant	SPATA13	GRCh38.p7	13:24086828	CATTGCTGGCTTCAG[C/G]TGCTGCCACTACCCA	221178
rs912137	snp	G/T	0.5	0.00019968	intron-variant	SPATA13	GRCh38.p7	13:24086827	ATTGCTGGCTTCAGC[G/T]GCTGCCACTACCCAG	221178
rs912138	snp	C/G	0.250168	0.25	intron-variant	SPATA13	GRCh38.p7	13:24086557	TCGCCAGTCCCCAAG[C/G]CTACAGACCCAGCCA	221178
rs912139	snp	A/G	0.24449	0.249939	intron-variant	SPATA13	GRCh38.p7	13:24085873	TGCGCCCTGGTTCCG[A/G]TGCTTTGCACTATTA	221178
rs912140	snp	A/G	0.0372196	0.131242	intron-variant	SPATA13	GRCh38.p7	13:24084745	GATGTGAGCCACTGC[A/G]CTGCGCCACTTCATT	221178
rs912141	snp	C/T	0.404209	0.196773	intron-variant	SPATA13, SPATA13-AS1	GRCh38.p7	13:24253297	ATTTCCAAAGAGTGT[C/T]ATTCTAATGACACTC	221178
rs912142	snp	A/G	0.404559	0.196498	intron-variant	SPATA13, SPATA13-AS1	GRCh38.p7	13:24253362	TCTCTCTTCCCTAGA[A/G]GGAGACACCCAGATC	221178
rs912143	snp	C/T	0.336245	0.234652	intron-variant	SPATA13, SPATA13-AS1	GRCh38.p7	13:24253606	AACAGATTCCATAAG[C/T]CAATATGTAGGATGC	221178
rs912144	snp	C/T	0.405429	0.195811	intron-variant, upstream-variant-2KB	SPATA13, SPATA13-AS1	GRCh38.p7	13:24254522	CTTCCTTCTCTGTGA[C/T]GTTCTGGGCCTGGAT	221178
rs912145	snp	A/G	0.405603	0.195673	intron-variant, upstream-variant-2KB	SPATA13, SPATA13-AS1	GRCh38.p7	13:24254541	CTGGGCCTGGATGGC[A/G]TGTGAGATGCTGCGA	221178
rs912146	snp	A/G	0.345704	0.230956	intron-variant, upstream-variant-2KB	SPATA13, SPATA13-AS1	GRCh38.p7	13:24254689	TGCAATCAGCTTTCC[A/G]CAAGGGGCTGTCTGG	221178
rs912147	snp	A/G	0.210605	0.246877	intron-variant	SPATA13	GRCh38.p7	13:24204210	TACAGGAATAATACC[A/G]TTTAATTCTCACTGC	221178
rs912148	snp	C/T	0.21303	0.247251	intron-variant	SPATA13	GRCh38.p7	13:24204247	CCAGAGTCTCTGTTA[C/T]TGTTATCCACATTTT	221178
rs912149	snp	A/G	0.213333	0.247296	intron-variant	SPATA13	GRCh38.p7	13:24204307	CACTGTGTTCAGAAA[A/G]CGATAGGAAAATTGT	221178
rs912150	snp	A/G	0.442791	0.15916	intron-variant	SPATA13	GRCh38.p7	13:24078747	GCATGGAATGGGAAG[A/G]TGAATGTACACTGAT	221178
rs912151	snp	A/G	0.397452	0.201886	intron-variant	SPATA13	GRCh38.p7	13:24078410	CATATACTTCAGACT[A/G]TTACTGTGAGTCTTC	221178
rs912863	snp	A/G	0.153332	0.230554	intron-variant	SPATA13	GRCh38.p7	13:24099548	TGTGCTTCAGACCCC[A/G]TGCATCCACAAGCAC	221178
rs912864	snp	C/T	0.0444908	0.142359	intron-variant	SPATA13	GRCh38.p7	13:24083434	GGGCAGGCCTGACCT[C/T]GGCCACAGGTGCTGC	221178
rs912865	snp	C/T	0.498084	0.0308911	intron-variant	SPATA13	GRCh38.p7	13:24041910	TACATTCCAATTGAC[C/T]GTTACGCCTCACTCT	221178
rs912866	snp	A/G	0.498084	0.0308911	intron-variant	SPATA13	GRCh38.p7	13:24041904	CCAATTGACCGTTAC[A/G]CCTCACTCTGATTCC	221178
rs912867	snp	C/T	0.498109	0.0306926	intron-variant	SPATA13	GRCh38.p7	13:24041803	CCCTTACCTGTCTCA[C/T]GCTTTCCCACCTTCC	221178
rs912868	snp	A/T	0.5	0.000399361	intron-variant	SPATA13	GRCh38.p7	13:23990463	GTGCTGAAACAAGGG[A/T]GCACCCTGAGTTTAA	221178
rs912869	snp	C/G	0.498253	0.0295011	intron-variant	SPATA13	GRCh38.p7	13:23990216	GATCATAAAACTGCT[C/G]AATGTGGAAAAGTCT	221178
rs912870	snp	C/T	0.242488	0.249887	intron-variant	SPATA13	GRCh38.p7	13:24011946	TGTGCACCTCCGCCT[C/T]CCCCTACGGATTGTA	221178
rs912871	snp	A/G	0.0490535	0.14873	intron-variant	SPATA13	GRCh38.p7	13:24012660	CCGTCTTCCGCAGCC[A/G]ACCCCCAAGTGTGTG	221178
rs927552	snp	A/G	0.487241	0.0788465	intron-variant	SPATA13	GRCh38.p7	13:24234367	TTCCATATTCTTCAG[A/G]GGGGGAATTTTAGCT	221178
rs927553	snp	C/G	0.49089	0.0668743	intron-variant	SPATA13	GRCh38.p7	13:24234566	AGAAGGAATGCCGTA[C/G]GTTTTGTTGGTGGGG	221178
rs927764	snp	A/G	0.0433465	0.140692	intron-variant	SPATA13	GRCh38.p7	13:23989816	gcaccaaccctgttc[A/G]tcaggcttctgtcct	221178
rs942109	snp	C/T	0.225597	0.248806	intron-variant	SPATA13	GRCh38.p7	13:24065868	GCTCTGAAGTCCAAA[C/T]ACTTGGGTTTGAATC	221178
rs942110	snp	C/T	0.225301	0.248777	intron-variant	SPATA13	GRCh38.p7	13:24065904	TCTGCCACTTAACAA[C/T]TTGACTTGTCTTGGA	221178
rs942872	snp	C/T	0.0700422	0.173537	intron-variant	SPATA13	GRCh38.p7	13:24058384	CCGTAATCCCTTCAG[C/T]AGGGAATTCTGATAT	221178
rs942875	snp	A/G	0.382279	0.212137	intron-variant	SPATA13	GRCh38.p7	13:24040611	GGGGTCCAGGACACA[A/G]AGCCTGCCAAGCACC	221178
rs942876	snp	A/G	0.448066	0.152544	intron-variant	SPATA13	GRCh38.p7	13:24040812	TGATTGTTTGCTGTC[A/G]TTCCTTTATAAAACT	221178
rs942877	snp	A/T	0.0452528	0.143452	intron-variant	SPATA13	GRCh38.p7	13:23990952	GCCAACTCAGCTTTC[A/T]CTTCTTGCCACACAG	221178
rs942878	snp	C/G	0.479984	0.0980171	intron-variant	SPATA13	GRCh38.p7	13:23990742	GGTTCTGGGTGATCA[C/G]GGGAAACAAGGTAGA	221178
rs942879	snp	C/G	0.491157	0.065903	intron-variant	SPATA13	GRCh38.p7	13:23990728	ACGGGAAACAAGGTA[C/G]ATGTGATCCTGCTCC	221178
rs942880	snp	A/G	0.348574	0.229746	intron-variant	SPATA13	GRCh38.p7	13:23986221	TGGAATTTGGCATAT[A/G]GTTTCCTTAGAAAGA	221178
rs942882	snp	A/C	0.482234	0.0925596	intron-variant	SPATA13	GRCh38.p7	13:24100130	TTTAAACTATTTAAA[A/C]ATTATAAAATAAATC	221178
rs947227	snp	A/G	0.496616	0.0409947	intron-variant	SPATA13	GRCh38.p7	13:24301932	AATCCCTAAAACGGG[A/G]ATTACAGTACCTATG	221178
rs947228	snp	C/T	0.49681	0.0398085	intron-variant	SPATA13	GRCh38.p7	13:24301891	GAGAATTAAATGAAT[C/T]AATAGAAGTAAAGTG	221178
rs947229	snp	C/T	0.496649	0.0407971	intron-variant	SPATA13	GRCh38.p7	13:24301652	AGAAGGCTCTCCCTA[C/T]CTCCCGAGGTGGCAG	221178
rs947230	snp	G/T	0.496842	0.0396107	intron-variant	SPATA13	GRCh38.p7	13:24300788	GGATGTGCGTGACCT[G/T]GTGGCTAACACCATC	221178
rs956382	snp	C/T	0.409212	0.192748	intron-variant	SPATA13	GRCh38.p7	13:24112821	AAGAATCTGAAGCAA[C/T]GACAGCAAAGACCAA	221178
rs958993	snp	A/G	0	0	intron-variant	SPATA13	GRCh38.p7	13:23996212	GGCCTCAGAAGGAAA[A/G]CAATCCTTGAGTCAG	221178
rs976418	snp	G/T	0.163564	0.234582	intron-variant	SPATA13	GRCh38.p7	13:24073847	CTCAGTTCACAGCCT[G/T]CCTGAATATTCATGG	221178
rs989513	snp	C/T	0.465158	0.127307	intron-variant	SPATA13	GRCh38.p7	13:24143453	CGCAGCTGCTGGCAG[C/T]GCTCTCATTCCTATG	221178
rs989514	snp	C/T	0.465473	0.126772	intron-variant	SPATA13	GRCh38.p7	13:24143502	AAATTGATAGTTACT[C/T]CTATTTTTGCAAAGA	221178
rs1001784	snp	A/C	0.272241	0.249009	intron-variant	SPATA13	GRCh38.p7	13:23980081	CGCACCTATAGCTCT[A/C]TCCCTTCTCCTACCC	221178
rs1012035	snp	A/G	0.488666	0.0744214	intron-variant	SPATA13	GRCh38.p7	13:24056430	GTCTTGTATGGAAAT[A/G]GAATAACAAGCCTAA	221178
rs1022825	snp	A/C	0.465263	0.127129	intron-variant	SPATA13	GRCh38.p7	13:24097163	AGCTGTCAGTGCACC[A/C]GGCATGGGTGGCTGG	221178
rs1022826	snp	C/G	0.434687	0.168495	intron-variant	SPATA13	GRCh38.p7	13:24097312	CTTACAAATGAGAAG[C/G]TAAATAATTTCCCCA	221178
rs1028695	snp	C/T	0.385932	0.209815	intron-variant	SPATA13	GRCh38.p7	13:24178628	ACTTAGTGAACCAAG[C/T]AGACCCAGTCTATCT	221178
rs1028696	snp	A/G	0.386313	0.209568	intron-variant	SPATA13	GRCh38.p7	13:24178795	agatctaattgatat[A/G]taacgcatccattta	221178
rs1028697	snp	C/T	0.474091	0.11083	intron-variant	SPATA13	GRCh38.p7	13:24178844	tttttagtgtatcca[C/T]ggagtcatgcactca	221178
rs1028698	snp	C/T	0.364401	0.222289	intron-variant	SPATA13	GRCh38.p7	13:24061807	aaataatctttacaa[C/T]aaactcctgagttta	221178
rs1028699	snp	A/T	0.358303	0.225323	intron-variant	SPATA13	GRCh38.p7	13:24061872	aacataaaagttttt[A/T]aaaaaaattaaaaat	221178
rs1028700	snp	A/G	0.252983	0.249982	intron-variant	SPATA13	GRCh38.p7	13:24062439	TCTCCAATGGCGCCA[A/G]GGTGCACGGTGCTGG	221178
rs1028701	snp	C/T	0.239902	0.249796	intron-variant	SPATA13	GRCh38.p7	13:24062671	ACCCAGTGAAGTATC[C/T]TCATGACTGCACCTG	221178
rs1033848	snp	A/C	0.463234	0.130503	intron-variant	SPATA13	GRCh38.p7	13:24140540	AGAGCTGTTTGGATC[A/C]AAATTCAGCCTCTCC	221178
rs1033849	snp	A/G	0.453939	0.144598	intron-variant	SPATA13	GRCh38.p7	13:24140628	GCGTGTCCTTCTGAG[A/G]CAGCTCTCAAGCTTT	221178
rs1033850	snp	C/T	0.469839	0.119042	intron-variant	SPATA13	GRCh38.p7	13:24140706	GCAGCGTATTTAAGT[C/T]AAAGAGCCAAGAATG	221178
rs1033851	snp	A/T	0.47023	0.118317	intron-variant	SPATA13	GRCh38.p7	13:24140729	CAAGAATGTTAGTAT[A/T]ATATAATGAAGTGAA	221178
rs1033852	snp	A/G	0.00953873	0.0683987	intron-variant	SPATA13	GRCh38.p7	13:24250615	TAAAAGGGAACTCCT[A/G]TGGAGTACTAGTACT	221178
rs1041131	snp	C/T	0.307423	0.243316	intron-variant	SPATA13	GRCh38.p7	13:23981879	AAAAGAAAATTGCAT[C/T]ACAGTTATTGTTTTT	221178
rs1113414	snp	A/G	0.414576	0.188188	intron-variant	SPATA13	GRCh38.p7	13:24053589	CTGGGCCCACGGTGG[A/G]AGTATTTTTCTCTAT	221178
rs1117357	snp	C/T	0.498568	0.0267188	intron-variant	SPATA13	GRCh38.p7	13:24047042	aatcagcagcactca[C/T]tccctagcctgctgt	221178
rs1124510	snp	C/G	0.0429648	0.14013	intron-variant	SPATA13	GRCh38.p7	13:24288370	TCATGACATTCAGTA[C/G]AATAAACTGACCATG	221178
rs1125959	snp	C/T	0.0689305	0.172377	intron-variant	SPATA13	GRCh38.p7	13:24061790	TTCATACCTGGGTGA[C/T]GAAATAATCTTTACA	221178
rs1129021	snp	A/G	0.417521	0.185571	utr-variant-3-prime, upstream-variant-2KB	SPATA13, C1QTNF9	GRCh38.p7	13:24305565	CCTGATTTGAGTCAC[A/G]TGTTCCACTTGGAAA	221178
rs1138013	snp	A/C/G	0.000399281	0.0141238	intron-variant	SPATA13	GRCh38.p7	13:24302297	AGAATTAGCTCTCTA[A/C/G]AAAAAAATATAAAAA	221178
rs1220545	snp	C/G	0.00329302	0.0404434	missense, intron-variant	SPATA13	GRCh38.p7	13:24223195	GTGCCCACCCCGAGC[C/G]GCCCCACTCCATGGT	221178
rs1220546	snp	C/T	0.412198	0.190241	synonymous-codon, intron-variant	SPATA13	GRCh38.p7	13:24223775	CAGGACGGCCCATGA[C/T]GCACGGGTACCACAG	221178
rs1220547	snp	C/T	0.497614	0.0344582	synonymous-codon, intron-variant	SPATA13	GRCh38.p7	13:24223982	GGCCAGCCTGAGACT[C/T]CAGGCACACAGCCGG	221178

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