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
rs6663	snp	C/T	0.299916	0.244966	intron-variant, utr-variant-3-prime, nc-transcript-variant	MYO1H, KCTD10	GRCh38.p7	12:109448798	TGCTGTCTTTAGGGC[C/T]CTACCCAAAGTCACT	83892
rs14064	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	KCTD10	GRCh38.p7	12:109450760	CCTTCCTGGAGTGGA[C/G]TCGGGTCAATCAGGA	83892
rs918106	snp	A/G	0.498589	0.02652	intron-variant	KCTD10	GRCh38.p7	12:109466513	TCACAGCCGACATTT[A/G]TGGAGCTCTGTCTAC	83892
rs918107	snp	A/G	0.269538	0.249235	intron-variant	KCTD10	GRCh38.p7	12:109466393	CAGTTATGAATGATA[A/G]TGTTTTGCAGAGTTG	83892
rs961269	snp	C/T	0.0402882	0.136092	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	UBE3B, KCTD10	GRCh38.p7	12:109477338	CGGCCCCGCCTCCGC[C/T]CCCGGCTGGCGTGAG	83892
rs1045582	snp	G/T	0.270621	0.249148	utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant	UBE3B, KCTD10	GRCh38.p7	12:109477922	GTGCTGGGATCTGGC[G/T]TGTGTGCTCCAGGGG	83892
rs1045857	snp	G/T	0.121717	0.214577	utr-variant-3-prime, nc-transcript-variant	KCTD10	GRCh38.p7	12:109449017	GTAATCAAGGGTTTT[G/T]TTTGTTTGTTTGTTT	83892
rs1073779	snp	C/T	0.269538	0.249235	intron-variant	KCTD10	GRCh38.p7	12:109456916	CAGCAATTCTGTTCC[C/T]AGAGAAATGAAAACG	83892
rs1073780	snp	C/T	0.198634	0.244666	intron-variant	KCTD10	GRCh38.p7	12:109457338	TTTCTTTTCAGGCAG[C/T]GAAAAAGTTCTAAAA	83892
rs1477117	snp	C/T	0.211516	0.24702	utr-variant-3-prime, nc-transcript-variant	KCTD10	GRCh38.p7	12:109450974	ATATGGCTGAATGAG[C/T]GTCTAAATCGTTGAG	83892
rs1558804	snp	C/T	0.5	0	intron-variant	KCTD10	GRCh38.p7	12:109460927	CAGGTGAGGCTGCCA[C/T]TCTCCAGGCAGTCCC	83892
rs1990714	snp	A/C	0.200492	0.245049	intron-variant	KCTD10	GRCh38.p7	12:109463206	GCCCTGGGTCTTCCC[A/C]AGCAGCTGAGTTCTG	83892
rs1990715	snp	A/G	0.109108	0.206518	intron-variant	KCTD10	GRCh38.p7	12:109462960	AGAACTGGTAGAAAG[A/G]TAATACGGTCTTTCC	83892
rs2058804	snp	C/T	0.244898	0.249948	intron-variant	KCTD10	GRCh38.p7	12:109471206	TTTACAAAAATAACG[C/T]TTGTGTTTTACCAGT	83892
rs2302703	snp	C/T	0.269538	0.249235	intron-variant	KCTD10	GRCh38.p7	12:109461027	AACAGAGCCTCAGAC[C/T]AGGGTCACCTGGGGT	83892
rs2302704	snp	C/T	0.271702	0.249056	intron-variant	KCTD10	GRCh38.p7	12:109460992	GTTGTGTCCAGCCAG[C/T]AGGGCCTGGAGGCTG	83892
rs2302705	snp	A/G	0.269538	0.249235	intron-variant	KCTD10	GRCh38.p7	12:109460911	TCTCCAGGCAGTCCC[A/G]CTCTCCGCTGGGAGG	83892
rs2302706	snp	C/T	0.271944	0.249035	synonymous-codon, nc-transcript-variant	KCTD10	GRCh38.p7	12:109456223	GTTCATAAAGGATGT[C/T]ATTGGGGATGAAATC	83892
rs2302707	snp	C/T	0.269538	0.249235	intron-variant	KCTD10	GRCh38.p7	12:109455992	TGCCTTGTGATTGCT[C/T]ATCCTTAAAATATTT	83892
rs2302708	snp	G/T	0.269538	0.249235	intron-variant	KCTD10	GRCh38.p7	12:109455921	TGGCATTCCTTTAGC[G/T]CCCTACCTTGCTGGC	83892
rs2302709	snp	C/T	0.269538	0.249235	intron-variant	KCTD10	GRCh38.p7	12:109455892	GCTTCCTTCCAAGCA[C/T]GCTTGACTCCCTGAC	83892
rs2338104	snp	C/G	0.497803	0.033074	intron-variant	KCTD10	GRCh38.p7	12:109457363	ctaaaattagatagt[C/G]gttatggcctcacaa	83892
rs3214388	in-del	-/A	0.124491	0.216211	utr-variant-3-prime, nc-transcript-variant	KCTD10	GRCh38.p7	12:109449957	TGACTGAATGTCAAA[-/A]TCGTGTATTGGGCAG	83892
rs3217162	in-del	-/GGC	0.499017	0.0221427	cds-indel, nc-transcript-variant	KCTD10	GRCh38.p7	12:109450354	TGGGGCACAGGTGGC[-/GGC]CCCTGCTGGAGCCCG	83892
rs3832870	in-del	-/CCTGAT	0.212728	0.247206	intron-variant	KCTD10	GRCh38.p7	12:109451899	TCCCAGGGGCCTGAT[-/CCTGAT]TTAGCCTGGCGGCCC	83892
rs3948619	snp	G/T	0.200801	0.245111	intron-variant	KCTD10	GRCh38.p7	12:109474712	AAGTGGGGGCTGGCT[G/T]TGGTTTATGGTGTTT	83892
rs4766473	snp	C/T	0.269809	0.249214	intron-variant	KCTD10	GRCh38.p7	12:109462791	CTGATTTTTAAAGGA[C/T]GGTAAACTAATTAAA	83892
rs4766474	snp	C/G	0.269538	0.249235	intron-variant	KCTD10	GRCh38.p7	12:109470279	AATGGGATTCCAGCT[C/G]GCACTCCTATCACTT	83892
rs4766475	snp	A/G	0.269538	0.249235	intron-variant	KCTD10	GRCh38.p7	12:109470568	AACTGTAGAGGTGGA[A/G]ATGTGCAAGGGTGGG	83892
rs4766601	snp	C/G	0.308661	0.24302	intron-variant	KCTD10	GRCh38.p7	12:109452275	TGGCCATTTAGGTCA[C/G]TGCTAATATGCTTCT	83892
rs4766602	snp	C/T	0.48692	0.0798058	intron-variant	KCTD10	GRCh38.p7	12:109452705	ACAGTGAGTTTACTG[C/T]TTGCTGCTGCCAGCA	83892
rs4766603	snp	C/T	0.269809	0.249214	intron-variant	KCTD10	GRCh38.p7	12:109454301	gagcaaatggaaaca[C/T]agggagtctcagcaa	83892
rs4766604	snp	C/T	0.27008	0.249192	intron-variant	KCTD10	GRCh38.p7	12:109454374	caataaccaacaacc[C/T]caaacaaaaacacaa	83892
rs4766605	snp	A/C	0.269538	0.249235	intron-variant	KCTD10	GRCh38.p7	12:109457831	GGGGACCACATGACC[A/C]AATAGCAGGGGCACA	83892
rs6606721	snp	A/G	0.269809	0.249214	intron-variant	KCTD10	GRCh38.p7	12:109454194	ctcacagatgctagc[A/G]ccaaggtgacacaag	83892
rs6606723	snp	C/G	0.269538	0.249235	intron-variant	KCTD10	GRCh38.p7	12:109467239	CAGCTTTTGAAAAAG[C/G]ATTTCACCTCTGAAA	83892
rs6606724	snp	C/T	0.269538	0.249235	intron-variant	KCTD10	GRCh38.p7	12:109467374	CCTGTAATCCCAGCA[C/T]TTTGGGAGGCTGAGG	83892
rs6606725	snp	A/C	0.49975	0.0111793	intron-variant	KCTD10	GRCh38.p7	12:109467563	GGAGATGGAGGCTGC[A/C]GTGAGCTATGATGGC	83892
rs7136048	snp	A/G	0.269538	0.249235	intron-variant	KCTD10	GRCh38.p7	12:109466121	GGCATGCTCACTGCC[A/G]CAGTGTCCTTGTCTT	83892
rs7139106	snp	A/G	0.269809	0.249214	intron-variant	KCTD10	GRCh38.p7	12:109470835	GCTTTACCAATGAGA[A/G]GTTTAGCCTCCTTCC	83892
rs7295954	snp	C/T	0.264084	0.249603	utr-variant-3-prime, nc-transcript-variant	KCTD10	GRCh38.p7	12:109450787	AGGAGAACAACTGGA[C/T]GGGGCTGGAGTTGGG	83892
rs7298476	snp	G/T	0.0792508	0.182605	intron-variant	KCTD10	GRCh38.p7	12:109471991	gaatggagtgtgtag[G/T]cctggaaattgctct	83892
rs7299041	snp	A/T	0.242488	0.249887	intron-variant	KCTD10	GRCh38.p7	12:109467223	CCTTTTCTAGTCCCA[A/T]CAGCTTTTGAAAAAG	83892
rs7308091	snp	C/G	0.0267878	0.112589	intron-variant	KCTD10	GRCh38.p7	12:109459099	aacagaatcatcaga[C/G]agttgagagcagata	83892
rs7313797	snp	C/T	0.5	0	intron-variant	KCTD10	GRCh38.p7	12:109458360	TCAAAAATAAACCCT[C/T]GACGTGGCAGCAGAA	83892
rs7315846	snp	C/T	0.270351	0.24917	intron-variant	KCTD10	GRCh38.p7	12:109470812	GGCTAATAGGAGTTA[C/T]AGCTGCTGCTTTACC	83892
rs7316375	snp	C/G	0.271702	0.249056	intron-variant	KCTD10	GRCh38.p7	12:109469193	TGGGGAGCTGAGACT[C/G]AAACCCAGGTTGGCA	83892
rs7959161	snp	A/G	0.0329836	0.124112	intron-variant, upstream-variant-2KB	UBE3B, KCTD10	GRCh38.p7	12:109478848	TTAAATAATCTGTGC[A/G]GTGTCTGATACACCG	83892
rs7967399	snp	C/T	0.0792508	0.182605	utr-variant-3-prime, nc-transcript-variant	KCTD10	GRCh38.p7	12:109450402	ACCCACAGTCACACA[C/T]ATCCCTTAAACAAAC	83892
rs7967695	snp	C/T	0.0792508	0.182605	intron-variant	KCTD10	GRCh38.p7	12:109463215	GCTGCTTGGGAAGAC[C/T]CAGGGCCCTGAAATC	83892
rs7969313	snp	A/G	0.271972	0.249033	intron-variant	KCTD10	GRCh38.p7	12:109469498	GCCAGAGGCAGGCAC[A/G]TGGTGGGTGAGCTTA	83892
rs7969549	snp	C/G	0.291235	0.246576	intron-variant	KCTD10	GRCh38.p7	12:109461108	ATATCCCTTACACAA[C/G]GACATCCAACAGGGG	83892
rs7970363	snp	A/G	0.0788843	0.182262	intron-variant	KCTD10	GRCh38.p7	12:109454527	tgaggccaggaggtc[A/G]agaccagcctgggca	83892
rs7979038	snp	A/G	0.0170251	0.090679	intron-variant	KCTD10	GRCh38.p7	12:109473907	ctgcctcaccctccc[A/G]agtagctgggattac	83892
rs9943689	snp	A/G	0.278399	0.248382	intron-variant	KCTD10	GRCh38.p7	12:109452534	TTCAGGGTGGAATTC[A/G]GAGGTTCTGGGAAAA	83892
rs9943724	snp	A/G	0.269809	0.249214	intron-variant	KCTD10	GRCh38.p7	12:109465098	GGGCAGCATCGCACA[A/G]AGAAACTCCCACGCA	83892
rs9943764	snp	A/G	0.269538	0.249235	intron-variant	KCTD10	GRCh38.p7	12:109467915	TCAGGCCACCAAGGC[A/G]AGGCCTTTCGAGGAG	83892
rs10160889	snp	A/G	0.0256215	0.110247	intron-variant	KCTD10	GRCh38.p7	12:109463172	GAAGGAACCTTCCAC[A/G]TTCTGCCTTTGATGT	83892
rs10583123	in-del	-/TTC	0.447291	0.153545	intron-variant	KCTD10	GRCh38.p7	12:109466588	ACATCAACATCCAAG[-/TTC]TTCTTGGTTTAGGAG	83892
rs10774708	snp	A/G	0.498346	0.0287064	intron-variant	KCTD10	GRCh38.p7	12:109455351	ACAGGGGAAATCACC[A/G]CACTATAATTCTGTG	83892
rs10850201	snp	C/G	0.256897	0.249905	intron-variant	KCTD10	GRCh38.p7	12:109465257	ATGTCTGAACGAGAG[C/G]TATTTAGTTGTGGAT	83892
rs10850219	snp	C/G	0.251578	0.249995	intron-variant	KCTD10	GRCh38.p7	12:109471709	GTGAAGACCTCGAAG[C/G]GGGGGAGAAAAGGCT	83892
rs10850234	snp	A/C	0.255782	0.249933	upstream-variant-2KB, intron-variant	UBE3B, KCTD10	GRCh38.p7	12:109476890	CATTTTCCACCCCCA[A/C]ATGTCCGTTTTCAAT	83892
rs11066686	snp	C/T	0.200801	0.245111	intron-variant	KCTD10	GRCh38.p7	12:109457423	GAATATAATAATAAC[C/T]GTACACTCTAGAAAG	83892
rs11066696	snp	A/G	0.20111	0.245173	intron-variant	KCTD10	GRCh38.p7	12:109459346	TAGACTAACAGAAAC[A/G]AGACCCAGGGGCATG	83892
rs11066707	snp	A/G	0.0659589	0.169201	intron-variant	KCTD10	GRCh38.p7	12:109460568	CCCATTTTGCAGAGA[A/G]GGAAAATGAGGAAGG	83892
rs11066714	snp	C/T	0.190205	0.242744	intron-variant	KCTD10	GRCh38.p7	12:109461409	TGACCAAGACAGACC[C/T]CACCCTCAGGCAGCT	83892
rs11066718	snp	C/G	0.200801	0.245111	intron-variant	KCTD10	GRCh38.p7	12:109462026	TCCACGTCCTCCTCA[C/G]ACTGGGCCCTACTGA	83892
rs11066736	snp	A/G	0.0221141	0.102801	intron-variant	KCTD10	GRCh38.p7	12:109466455	CACTTGTCCAATGTC[A/G]CATGACCAGTAAATG	83892
rs11066737	snp	A/G	0.269538	0.249235	intron-variant	KCTD10	GRCh38.p7	12:109466987	CTCTCTCCAAGGACC[A/G]ACAGGATCGCTCTGC	83892
rs11066782	snp	C/T	0.269538	0.249235	intron-variant	KCTD10	GRCh38.p7	12:109472747	ACTATCACTGGGCTA[C/T]AGGAATTTTTCAGTT	83892
rs11066788	snp	C/T	0.115088	0.210473	intron-variant	KCTD10	GRCh38.p7	12:109473508	AGCTCTAATGGCAGA[C/T]GGCATGACTAAGAGA	83892
rs11282253	in-del	-/ATCAGG			intron-variant	KCTD10	GRCh38.p7	12:109451905	CCAGGCTAAATCAGG[-/ATCAGG]CCCCTGGGATTCTGC	83892
rs11540748	snp	C/T	0.0517044	0.152246	utr-variant-3-prime, nc-transcript-variant	KCTD10	GRCh38.p7	12:109450895	GCCACCTTGGGCTGG[C/T]CTTTGGCCTGGTGCT	83892
rs11540749	snp	A/G	0.0520825	0.152737	utr-variant-3-prime, nc-transcript-variant	KCTD10	GRCh38.p7	12:109451081	CTGTGTGTTTGGCCC[A/G]GGCACAATCCCCACT	83892
rs11609019	snp	A/G	0.269538	0.249235	intron-variant	KCTD10	GRCh38.p7	12:109458153	TTGACCGGCTGGACA[A/G]GCTCTGGCGAGGGGA	83892
rs11610840	snp	C/T	0.269538	0.249235	intron-variant	KCTD10	GRCh38.p7	12:109456591	AGTGCTCCTAACCAT[C/T]GTGCTTGAGTGACAG	83892
rs11612500	snp	C/T	0.269809	0.249214	intron-variant	KCTD10	GRCh38.p7	12:109459331	ctggaggtctaacct[C/T]agactaacagaaACG	83892
rs11613021	snp	G/T	0.269538	0.249235	intron-variant	KCTD10	GRCh38.p7	12:109460193	TCTAGAAGCATTTTG[G/T]TTTTGTGGGATTTTA	83892
rs11613023	snp	C/T	0.269538	0.249235	intron-variant	KCTD10	GRCh38.p7	12:109460242	CCAGTGGTCCTGCTC[C/T]GTCTAGCTAAGGAGT	83892
rs11613718	snp	C/T	0.271702	0.249056	intron-variant	KCTD10	GRCh38.p7	12:109474527	CTGATGTAATTGGTC[C/T]GGGATGTGGACTAGG	83892
rs11613809	snp	C/T			intron-variant	KCTD10	GRCh38.p7	12:109469032	TATCTATCTATCTAT[C/T]TACACACACACATAT	83892
rs11614385	snp	A/C			intron-variant	KCTD10	GRCh38.p7	12:109470049	ACTGACCCTGCCTGT[A/C]GACCCTGCAGGCACA	83892
rs11615336	snp	A/C	0.268452	0.249318	upstream-variant-2KB, intron-variant	UBE3B, KCTD10	GRCh38.p7	12:109476997	TTCCTCACGCACACA[A/C]GTATCTACTCCGCAA	83892
rs11615949	snp	A/G	0.269809	0.249214	intron-variant	KCTD10	GRCh38.p7	12:109456542	ATAAATGGCAGACAC[A/G]CCCCCCAAAAGACAG	83892
rs11831213	snp	C/T	0.200906	0.245132	intron-variant	KCTD10	GRCh38.p7	12:109457551	CCTCATCTGAAGGTA[C/T]GAAGAAGAGCTGGGC	83892
rs12227283	snp	A/G	0.0659589	0.169201	intron-variant	KCTD10	GRCh38.p7	12:109458199	GCTGGGAAGAGAGAA[A/G]GATTCTCACCACCAG	83892
rs12427319	snp	A/G	0	0	utr-variant-3-prime, nc-transcript-variant	KCTD10	GRCh38.p7	12:109451027	TATCAACAAGCTCTA[A/G]GCCCAAAGCCACATG	83892
rs12578648	snp	A/G	0.290201	0.246747	intron-variant	KCTD10	GRCh38.p7	12:109453937	gcatggcacacagct[A/G]ggacagatttgaagg	83892
rs12582711	snp	C/T	0.0707826	0.174302	intron-variant	KCTD10	GRCh38.p7	12:109470119	TGCCTAGCACCTGTA[C/T]ACATGAACACCCTGG	83892
rs12818120	snp	C/T	0.269809	0.249214	intron-variant	KCTD10	GRCh38.p7	12:109464111	TCCTTTCCCCTCTCC[C/T]ACCACCTCCAGGGAA	83892
rs12818537	snp	C/T	0.269538	0.249235	intron-variant	KCTD10	GRCh38.p7	12:109464345	TAAGAGGCTGCCCCG[C/T]ACATTGTAGGGTATT	83892
rs12819142	snp	G/T	0.198634	0.244666	intron-variant	KCTD10	GRCh38.p7	12:109458511	AAAAGTCAAAAATTT[G/T]AGGGTAGAAAGGTCA	83892
rs12819658	snp	A/T	0.269538	0.249235	intron-variant	KCTD10	GRCh38.p7	12:109469865	TTGCTTCCAATGTGG[A/T]CAACTAAGGAGAGCT	83892
rs12819926	snp	A/G			intron-variant	KCTD10	GRCh38.p7	12:109467380	atcccagcattttgg[A/G]aggctgaggtgagag	83892
rs12821585	snp	C/T	0.0520825	0.152737	downstream-variant-500B	MYO1H, KCTD10	GRCh38.p7	12:109448556	CACCTGGAGCGACTT[C/T]AAGGGGCTGAGGCAG	83892
rs12822891	snp	A/G	0.271702	0.249056	intron-variant	KCTD10	GRCh38.p7	12:109458197	TGGCTGGGAAGAGAG[A/G]AGGATTCTCACCACC	83892
rs12822974	snp	G/T	0.48	0.0979796	intron-variant	KCTD10	GRCh38.p7	12:109471349	TGGCACCCAACAGTG[G/T]CCTGGATATCACCTG	83892
rs12823587	snp	A/G	0.269538	0.249235	intron-variant	KCTD10	GRCh38.p7	12:109458585	GGGCGGAAGCACTGG[A/G]AAGATCCCCAAATCC	83892
rs12831026	snp	C/T	0.269809	0.249214	intron-variant	KCTD10	GRCh38.p7	12:109465846	TTCTAGGGGAATGTG[C/T]GATCACAAAATGAAT	83892

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