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
rs10056	snp	G/T	0	0	stop-gained, nc-transcript-variant	RNF10	GRCh38.p7	12:120576601	TCTGAAGAGAAAGGA[G/T]GAAAGAAAAGAAAAA	9921
rs10505	snp	A/C	0	0	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120576998	CTGGGTTGGACTGCT[A/C]TAATGCATCTCAAAG	9921
rs488313	snp	C/T	0.0607341	0.163335	intron-variant	RNF10	GRCh38.p7	12:120573203	ccatattagatatta[C/T]tgtggcagtggaatt	9921
rs489854	snp	G/T	0.494272	0.053207	intron-variant	RNF10	GRCh38.p7	12:120567862	GCATTTCATTATGGg[G/T]gtgtgtgtgtgtgtg	9921
rs492574	snp	C/T	0.491525	0.0645418	intron-variant	RNF10	GRCh38.p7	12:120568155	TAGGCTCAAGCCATC[C/T]CCCCACCTCAGCCTC	9921
rs516479	snp	A/G	0.390838	0.206555	intron-variant	RNF10	GRCh38.p7	12:120568498	ACAGAGCTAGACTCC[A/G]TCTCAAAAAAAAAAA	9921
rs532725	snp	C/T	0.494442	0.0524218	intron-variant	RNF10	GRCh38.p7	12:120562271	TCTTTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT	9921
rs533843	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120559271	actgcaacctccacc[C/T]cctcggttcaaacga	9921
rs541126	snp	A/G	0.302936	0.244331	utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534593	ACCGAGGACGAGGAG[A/G]CCGGGGCTCGGGAGT	9921
rs546417	snp	A/C	0.421593	0.181813	intron-variant	RNF10	GRCh38.p7	12:120566787	AAAAAAAATTGAATT[A/C]TGTAAATGGGTTTAC	9921
rs560385	snp	A/G	0.0607341	0.163335	intron-variant	RNF10	GRCh38.p7	12:120559891	taatagaaacagggt[A/G]tctctatgttggcca	9921
rs567156	snp	C/T	0.337614	0.234145	intron-variant	RNF10	GRCh38.p7	12:120566573	GGTTTCACCATGTTG[C/T]CCAGCCTGGTCTTGA	9921
rs568055	snp	A/T	0	0	intron-variant	RNF10	GRCh38.p7	12:120543244	CTGATATAACTATAC[A/T]AAAGTACCTGTCTGC	9921
rs568058	snp	C/T	0.0217236	0.101931	intron-variant	RNF10	GRCh38.p7	12:120566657	ctcccacctcagcct[C/T]ccgagtagccgggac	9921
rs574858	snp	C/T	0.398714	0.200958	intron-variant	RNF10	GRCh38.p7	12:120572893	aaaaaaaaggccagg[C/T]gcagtggttcatgtc	9921
rs585510	snp	C/T	0.391024	0.206427	intron-variant	RNF10	GRCh38.p7	12:120562330	ccgagatcacgccac[C/T]gcactccagcctggg	9921
rs603574	snp	C/T	0.393803	0.204501	intron-variant	RNF10	GRCh38.p7	12:120560640	TTTCAAATACAGCCT[C/T]TTCTCTGGGGTGAAA	9921
rs608724	snp	A/G	0.498734	0.0251279	intron-variant	RNF10	GRCh38.p7	12:120574045	GGGACCTAATGGGAG[A/G]TGTATGGGTCATGGG	9921
rs614053	snp	C/T	0.0607341	0.163335	intron-variant	RNF10	GRCh38.p7	12:120548950	gggcgcggtggctca[C/T]gcctgtaatcccagc	9921
rs614226	snp	C/T	0.296109	0.245711	intron-variant	RNF10	GRCh38.p7	12:120536707	TTAGAGTGGTCTGTT[C/T]AAAGCAATTGATAAG	9921
rs630654	snp	C/T	0.0614824	0.164198	intron-variant	RNF10	GRCh38.p7	12:120547574	aggtgtggtggctca[C/T]gcctgtaatcccagc	9921
rs651627	snp	A/G	0.389152	0.207694	intron-variant	RNF10	GRCh38.p7	12:120571395	TCAATTTGTCCAGCC[A/G]TATTAGAATGAGAGG	9921
rs787829	snp	C/T	0.49614	0.0437598	intron-variant	RNF10	GRCh38.p7	12:120545273	gcaagctctgcctcc[C/T]ggggttcacgccgtt	9921
rs787830	snp	C/G	0.378765	0.214288	intron-variant	RNF10	GRCh38.p7	12:120548388	gTCTGGATAAGAAAC[C/G]AGCAGAAGAGAGCAC	9921
rs787831	snp	A/G	0.382279	0.212137	intron-variant	RNF10	GRCh38.p7	12:120548939	cctcccaaagtgctg[A/G]gattacaggcgtgag	9921
rs787832	snp	A/G	0.335559	0.234904	intron-variant	RNF10	GRCh38.p7	12:120548998	attagggaaatgata[A/G]catgtctgtgctcat	9921
rs787833	snp	A/C	0.398354	0.201224	intron-variant	RNF10	GRCh38.p7	12:120549818	aataaataataaata[A/C]aAATTTAAAAAAGGA	9921
rs787834	snp	C/T	0.382279	0.212137	intron-variant	RNF10	GRCh38.p7	12:120550657	gctagagtgcagtgg[C/T]gtgatcttggctcac	9921
rs787835	snp	C/T	0.030278	0.119257	intron-variant	RNF10	GRCh38.p7	12:120550665	gcagtggcgtgatct[C/T]ggctcactgccagct	9921
rs787947	snp	C/T	0.498852	0.0239341	intron-variant	RNF10	GRCh38.p7	12:120568926	CATCAAAAAGTATCT[C/T]TCttggccaggtaca	9921
rs787949	snp	C/T	0.0204374	0.0990014	intron-variant	RNF10	GRCh38.p7	12:120560678	AACATTCAAAGCTCA[C/T]GATGGTGTAGCTAAA	9921
rs812018	snp	A/G	0	0	intron-variant	RNF10	GRCh38.p7	12:120550724	gcctcagcctcccga[A/G]tagctgggactatag	9921
rs1043097	snp	C/T	0	0	utr-variant-5-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120534781	CGCGCCCGCTCCGCT[C/T]CGACTGCCGTCGCCG	9921
rs1137266	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120567448	tggcttatgcctgta[A/G]tcccagcactttggg	9921
rs1137270	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120567519	CAGCCTGACCAACAC[A/G]GTGAAACCCTATCTC	9921
rs1137272	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120567543	ctatctctactgaaa[A/G]tgcaaaaattagcag	9921
rs1137273	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120567547	ctctactgaaagtgc[A/G]aaaattagcagggca	9921
rs1137274	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120567548	tctactgaaagtgca[A/G]aaattagcagggcat	9921
rs1137275	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120567608	tgggaggctgaggca[A/G]cagaattgcttgaac	9921
rs1167711	snp	C/G	0.49614	0.0437598	intron-variant	RNF10	GRCh38.p7	12:120551823	TTAAAGACtgtatta[C/G]tccattctctcattg	9921
rs1167712	snp	G/T	0.496649	0.0407971	intron-variant	RNF10	GRCh38.p7	12:120553653	catgatccacccgcc[G/T]cggcctcccaaagtg	9921
rs1167713	snp	C/T	0.398714	0.200958	intron-variant	RNF10	GRCh38.p7	12:120554210	atgcctggcctaatt[C/T]ttctatttttagtag	9921
rs1167714	snp	A/G	0.382473	0.212016	intron-variant	RNF10	GRCh38.p7	12:120555262	tcttggctcactgca[A/G]cctctgcctccaggg	9921
rs1167715	snp	A/G	0.398534	0.201091	intron-variant	RNF10	GRCh38.p7	12:120543668	ggactccaggcatat[A/G]caccattcttggctt	9921
rs1167716	snp	C/T	0.398534	0.201091	intron-variant	RNF10	GRCh38.p7	12:120543607	gccatgttgcccaga[C/T]gggtctcaaactcct	9921
rs1167717	snp	C/T	0.0197687	0.0974348	intron-variant	RNF10	GRCh38.p7	12:120542380	gatcacttgagtcca[C/T]gagtttgcgaccagc	9921
rs1167718	snp	G/T	0.498547	0.0269177	intron-variant	RNF10	GRCh38.p7	12:120541591	aaaaattagccaggc[G/T]tggtggcgggcgcct	9921
rs1167719	snp	C/T	0.382279	0.212137	intron-variant	RNF10	GRCh38.p7	12:120540936	CCCGGGAGGTGGAGG[C/T]TGCGGCAAGGCCGAG	9921
rs1167720	snp	C/T	0.382279	0.212137	intron-variant	RNF10	GRCh38.p7	12:120540898	CACTACACTCCAGCC[C/T]GGGCAACAAGAGCAA	9921
rs1167721	snp	C/T	0.382279	0.212137	intron-variant	RNF10	GRCh38.p7	12:120540015	GAAACCCATCTCTAC[C/T]AAAAATACAAAAATT	9921
rs1167722	snp	C/T	0.382279	0.212137	intron-variant	RNF10	GRCh38.p7	12:120539995	ATACAAAAATTAGGC[C/T]GGTGTGGTGGTGGAC	9921
rs1167723	snp	C/T	0.378765	0.214288	intron-variant	RNF10	GRCh38.p7	12:120539578	AGCTAGAAATGAAGA[C/T]GCCAAGTAATTTAAC	9921
rs1167757	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120543980	tcggcctcccaaagt[A/G]ctgggattacaggca	9921
rs1167758	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120543968	agtactgggattaca[A/G]gcatgagccaccatg	9921
rs1184538	snp	C/T	0.49614	0.0437598	intron-variant	RNF10	GRCh38.p7	12:120551380	gctcactgcaacctc[C/T]gcctctcgggttcaa	9921
rs1710138	snp	A/T	0	0	intron-variant	RNF10	GRCh38.p7	12:120538788	GGTATTATGAGGCAG[A/T]TATTTTGAGGTTGGT	9921
rs2280168	snp	C/T	0.241141	0.249849	intron-variant	RNF10	GRCh38.p7	12:120571155	TGATTATATTCGTCA[C/T]GTTCCAAGGGGTGTC	9921
rs2292680	snp	A/C	0.383439	0.21141	intron-variant	RNF10	GRCh38.p7	12:120575345	TCTTACTGAGACCCT[A/C]AAATTGGGAATTCCG	9921
rs2292681	snp	C/T	0.47201	0.114942	intron-variant	RNF10	GRCh38.p7	12:120557529	TGAAACATGGACACT[C/T]ATATGTAGCAGGGCA	9921
rs2673626	snp	G/T	0	0	intron-variant	RNF10	GRCh38.p7	12:120553557	acaaaattagccagg[G/T]ggtgggcgcctgtag	9921
rs2743850	snp	A/G	0.00636936	0.0560724	intron-variant	RNF10	GRCh38.p7	12:120567745	AAAGAAGGGAATGTA[A/G]TTCTTCTATTCACGT	9921
rs3049456	in-del	-/A/AA/AAA	0.444133	0.157519	intron-variant	RNF10	GRCh38.p7	12:120541437	aaaaaaaaaaaaaaa[-/A/AA/AAA]ggaaaaCTCAGGGGA	9921
rs3049489	in-del	-/T/TT	0	0	intron-variant	RNF10	GRCh38.p7	12:120541452	ttttttttttttttt[-/T/TT]gagacggagtctcac	9921
rs3049493	in-del	-/TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	0	0	intron-variant	RNF10	GRCh38.p7	12:120553069	TTTTTTTTTTTTTTT[lengthTooLong]GAGATGTAGTCTCGC	9921
rs3088345	snp	C/G	0.383439	0.21141	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120577038	CACTGCTCTGCTGTA[C/G]CATCATGTCAGGGCT	9921
rs3168677	snp	C/G	0	0	intron-variant	RNF10	GRCh38.p7	12:120555146	TCAAAGTAGGCCTCA[C/G]CCTTGTGGCAGGGAG	9921
rs3203671	snp	C/T	0.00358779	0.0422022	utr-variant-3-prime, nc-transcript-variant	RNF10	GRCh38.p7	12:120576719	ACAAAAGCATGGGGG[C/T]AAAAAAAACAAAAAC	9921
rs3213565	snp	A/G	0.390651	0.206682	intron-variant	RNF10	GRCh38.p7	12:120554598	GCAGCCCTGGTTCAT[A/G]AGGCACTGCACTAGG	9921
rs3817301	snp	C/T	0.136506	0.222754	intron-variant, downstream-variant-500B	RNF10	GRCh38.p7	12:120576224	GCCACCCTGTACCAA[C/T]TCAAGATTCTAAAGG	9921
rs3817302	snp	A/G	0.000798403	0.0199641	intron-variant	RNF10	GRCh38.p7	12:120560530	TAAGAAATCTAAGAA[A/G]CCCAGAGATGTAGTC	9921
rs3999427	snp	G/T			intron-variant	RNF10	GRCh38.p7	12:120550770	ctaatttttttattt[G/T]tatttttagtagaga	9921
rs4102203	snp	A/G	0.121369	0.214369	intron-variant	RNF10	GRCh38.p7	12:120538568	GATATTTACTGCTGC[A/G]TGTTCTCAGAAATAC	9921
rs4347449	snp	A/C	0.334412	0.235318	intron-variant	RNF10	GRCh38.p7	12:120556414	cgggtacctgtagtc[A/C]cagctacttgggagg	9921
rs4766969	snp	A/G	0.393619	0.204631	intron-variant	RNF10	GRCh38.p7	12:120550435	TTGTTGACTGAGCAC[A/G]AGCTCTTAGATCTAA	9921
rs4767910	snp	C/T	0.39121	0.2063	intron-variant	RNF10	GRCh38.p7	12:120553437	AGACAAAGTCTTGCT[C/T]TGTCACCCAGGCTGG	9921
rs4767912	snp	A/G	0.393803	0.204501	intron-variant	RNF10	GRCh38.p7	12:120543399	GCTTATAATCCCAGC[A/G]CTTTGGGAGGCTGAG	9921
rs4767913	snp	C/T	0.243633	0.249919	intron-variant	RNF10	GRCh38.p7	12:120548412	AGAGCACAGTCAGGG[C/T]GGGAGGAAAATTGCT	9921
rs4767914	snp	C/T	0.391024	0.206427	intron-variant	RNF10	GRCh38.p7	12:120556014	GGCTTGTCTCAAACT[C/T]CCAGCTTCAAGTGAT	9921
rs4767915	snp	A/G	0.24449	0.249939	intron-variant	RNF10	GRCh38.p7	12:120561324	AGGAGTACCTGAAAC[A/G]GCAAGAATTACACAA	9921
rs5801387	in-del	-/T	0.42574	0.177808	intron-variant	RNF10	GRCh38.p7	12:120540131	TAGGAATTTATTATC[-/T]TTTTTTTTTTTGTAG	9921
rs5801391	in-del	-/T	0	0	intron-variant	RNF10	GRCh38.p7	12:120548676	TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCGC	9921
rs7133978	snp	A/T	0.334871	0.235153	intron-variant	RNF10	GRCh38.p7	12:120559059	attaacttttaattt[A/T]aaattatttttttta	9921
rs7138112	snp	C/T	0.496105	0.0439572	intron-variant	RNF10	GRCh38.p7	12:120559934	actcctaacttcagg[C/T]gatccacctgcctca	9921
rs7299954	snp	C/T	0.256619	0.249912	intron-variant	RNF10	GRCh38.p7	12:120558790	ttggcaggctagtct[C/T]gaactcccgagctca	9921
rs7488320	snp	G/T	0.391024	0.206427	intron-variant	RNF10	GRCh38.p7	12:120543827	aaaaattagctgggt[G/T]tggtggtgcacacct	9921
rs7956232	snp	A/G	0.00795532	0.062565	intron-variant	RNF10	GRCh38.p7	12:120563751	TGGGCATGGGGAGGG[A/G]TGGGGAGCCTCCTGG	9921
rs7956884	snp	C/T	0.0566069	0.158427	intron-variant	RNF10	GRCh38.p7	12:120556361	aacacggtgaaaccc[C/T]gtctctactaaaaaa	9921
rs7956998	snp	A/G	0.337386	0.23423	intron-variant	RNF10	GRCh38.p7	12:120557129	CATACATGTACCTAC[A/G]TTGTAAACAATTTTA	9921
rs7961574	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120545435	ctgacctcgtgatcc[A/G]cccacctcggcctcc	9921
rs7962410	snp	C/T	0.254664	0.249956	intron-variant	RNF10	GRCh38.p7	12:120545436	tgacctcgtgatccg[C/T]ccacctcggcctccc	9921
rs7966798	snp	A/G	0.00676609	0.0577691	intron-variant	RNF10	GRCh38.p7	12:120541560	ctgcctcagcctccc[A/G]agcagctgggactac	9921
rs7970747	snp	A/G	0.0729998	0.176553	intron-variant	RNF10	GRCh38.p7	12:120542453	gccaccaagtccagc[A/G]CTGAAACTTTGCTTT	9921
rs7970776	snp	A/G	0.0729998	0.176553	intron-variant	RNF10	GRCh38.p7	12:120569027	ccaggctggagtgca[A/G]tagtgcaatctcagc	9921
rs7971844	snp	C/T			intron-variant	RNF10	GRCh38.p7	12:120542660	cgggttcaaatgatt[C/T]tcatgccttagcctc	9921
rs7972244	snp	A/G	0.337614	0.234145	intron-variant	RNF10	GRCh38.p7	12:120557069	GAATGGCGTGAACCA[A/G]GGAGATGGACCGTCT	9921
rs7973555	snp	G/T	0.269809	0.249214	intron-variant	RNF10	GRCh38.p7	12:120568824	gctgtgatgcattca[G/T]tagctcactgcagtc	9921
rs7973558	snp	C/T	0.00358779	0.0422022	intron-variant	RNF10	GRCh38.p7	12:120538742	ATCCCCCTGGGCCGA[C/T]AGAACTGCCAGGGAG	9921
rs9669663	snp	C/T	0.382279	0.212137	intron-variant	RNF10	GRCh38.p7	12:120557016	GAGCGTGGTGGCAGG[C/T]GCCTGTAGTCCCAGC	9921
rs9705874	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120557101	aaaaaaaaaaaaaaa[A/G]gaaaaaaaTGATCAT	9921
rs9706503	snp	A/G			intron-variant	RNF10	GRCh38.p7	12:120557102	aaaaaaaaaaaaaaa[A/G]aaaaaaaTGATCATA	9921

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