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
rs471429	snp	C/G	0.345704	0.230956	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087885	AAAAGAAATCTCCCT[C/G]ACTAAAAATATGATC	154214
rs472505	snp	G/T	0.0584853	0.160693	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125088070	ATGTTGCCCAGGCTG[G/T]TCTCAAACTCTTGGG	154214
rs473130	snp	A/G	0.0667028	0.170006	intron-variant	RNF217	GRCh38.p7	6:125055265	GGGGCAGTCTCTCAA[A/G]TGAATACAAATAAGT	154214
rs473306	snp	C/G	0.223522	0.248594	intron-variant	RNF217	GRCh38.p7	6:125031244	gatgctaggagctgc[C/G]atgaaggcctctgac	154214
rs474025	snp	A/G	0.498206	0.0298983	intron-variant	RNF217	GRCh38.p7	6:125051280	AGACCCAATGACAAT[A/G]GGATAAAGGGAAAAC	154214
rs475076	snp	A/G	0.0150982	0.0855637	missense, nc-transcript-variant	RNF217	GRCh38.p7	6:125057966	CCTACCTGCCAATTC[A/G]TCTGGTGTTTTAAGT	154214
rs475133	snp	C/T	0.107694	0.205546	intron-variant	RNF217	GRCh38.p7	6:125031412	TTTTCCAAACATTTA[C/T]GCTGTTTCCCTTTTA	154214
rs476080	snp	C/T	0.101301	0.200969	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081863	ATCAAGGAAAAGAAG[C/T]TCTGCACCTTATGTG	154214
rs478591	snp	C/T	0.0535932	0.154675	intron-variant	RNF217	GRCh38.p7	6:125051756	CCTCTTGCTACTTTA[C/T]GTGGGTACCTCTTGT	154214
rs478948	snp	C/T	0.489201	0.0726845	intron-variant	RNF217	GRCh38.p7	6:125031885	tccattttcacactt[C/T]tgacaaagacataca	154214
rs479063	snp	C/T	0.0670745	0.170406	intron-variant	RNF217	GRCh38.p7	6:125077228	TCCTCCACTCATTCA[C/T]GGAGGACCTGCAATA	154214
rs482014	snp	C/T	0.49607	0.0441545	intron-variant	RNF217	GRCh38.p7	6:125044149	AGTCTTCATAGCATG[C/T]TTTTCTACTCCAAGT	154214
rs484003	snp	A/G	0.109814	0.206997	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125092107	TTCCTGCCAACAGGT[A/G]GGTCCTGCTGGACAG	154214
rs484433	snp	C/T	0.101658	0.201233	intron-variant	RNF217	GRCh38.p7	6:125082771	TCTTCTTTGTATGTT[C/T]GTACACTGCAAATAA	154214
rs484636	snp	A/G	0.479258	0.0997024	intron-variant	RNF217	GRCh38.p7	6:125071253	AATTCAAAATTTGAA[A/G]TATGGTTTCTACCAA	154214
rs484822	snp	C/T	0.0505692	0.150756	intron-variant	RNF217	GRCh38.p7	6:125077886	GTGAACCATTTTCCT[C/T]CTTAGAAGCATATGA	154214
rs485640	snp	A/T	0.499987	0.00259581	intron-variant	RNF217	GRCh38.p7	6:125044502	CCTCCCTTCTCTCCT[A/T]ATCTAGCTTCGTAGT	154214
rs487403	snp	A/G	0.0704125	0.17392	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087572	TGGAGACAGTATACA[A/G]AGTTAAAGCAACTGA	154214
rs489245	snp	A/G	0.0667028	0.170006	intron-variant	RNF217	GRCh38.p7	6:125054333	TGAGGTTTAGTCTAA[A/G]GCTCCATGGGGAGCA	154214
rs491270	snp	A/T	0.477768	0.103061	intron-variant	RNF217	GRCh38.p7	6:125070258	tccactcattgattg[A/T]tgggtacttagattg	154214
rs492800	snp	C/T	0.499928	0.00598999	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081565	GCCATAGAGAGAATA[C/T]GAGTGTAAATGTAAT	154214
rs494856	snp	A/G	0.477768	0.103061	intron-variant	RNF217	GRCh38.p7	6:125073609	TTTCTTGCCCAAATC[A/G]TGATTTGTTGGTAAC	154214
rs495548	snp	C/T	0.485118	0.0849685	intron-variant	RNF217	GRCh38.p7	6:125073628	TTTGTTGGTAACTCT[C/T]GACCCTAGGTGCTTA	154214
rs495860	snp	C/G	0.0995161	0.199636	intron-variant	RNF217	GRCh38.p7	6:125075899	CATATATAACATACA[C/G]TGTGGTAGTCACCGC	154214
rs496878	snp	G/T	0.0670745	0.170406	intron-variant	RNF217	GRCh38.p7	6:125075790	GAAAGATATTGTATA[G/T]AAATTAGAGCCATCT	154214
rs497277	snp	G/T	0.447162	0.153712	intron-variant	RNF217	GRCh38.p7	6:125054956	TATCTCACAACCACA[G/T]ACCCACCACATGGAG	154214
rs497574	snp	A/G	0.482534	0.0918038	intron-variant	RNF217	GRCh38.p7	6:125075764	CATCTTTATCTGTGC[A/G]TACTTTGTTGCATGA	154214
rs497969	snp	C/T	0.109461	0.206758	intron-variant	RNF217	GRCh38.p7	6:125038895	aaccaccatggcaca[C/T]gtttacctatgcaac	154214
rs499176	snp	A/C	0.487305	0.0786545	intron-variant	RNF217	GRCh38.p7	6:125058280	AAAATTTTTATAAAC[A/C]ATGTATATTCTTATT	154214
rs500439	snp	C/T	0.0648419	0.167978	intron-variant	RNF217	GRCh38.p7	6:125079329	AAAAATTCTAAGTTT[C/T]AAATCAAGTCGTATA	154214
rs501934	snp	A/G	0.109814	0.206997	intron-variant	RNF217	GRCh38.p7	6:125031997	AAAGGCACTCCTTAC[A/G]TGGCAGCAGCAAGAG	154214
rs502056	snp	C/T	0.482234	0.0925596	intron-variant	RNF217	GRCh38.p7	6:125065166	CGTAGTGGCAGTCGC[C/T]TGTAGTCCCAGCTAC	154214
rs502837	snp	C/T	0.108402	0.206034	intron-variant	RNF217	GRCh38.p7	6:125032094	tagcatgggaaagac[C/T]ggccccccatgattc	154214
rs502889	snp	A/G	0.143284	0.226079	intron-variant	RNF217	GRCh38.p7	6:125027007	aaatgttaaaaaata[A/G]tttaaaaaatttaaa	154214
rs502940	snp	A/T	0.155987	0.23165	intron-variant	RNF217	GRCh38.p7	6:125026995	ATAGTTTAAAAAATT[A/T]AAAAAAGAATGGTAC	154214
rs503812	snp	A/C	0.14665	0.227637	intron-variant	RNF217	GRCh38.p7	6:125042744	GCCTTGGATTGCTCT[A/C]GTCCCTAAACTGCAT	154214
rs503819	snp	C/T	0.452227	0.146984	intron-variant	RNF217	GRCh38.p7	6:125058788	CCAGAAAACTTTGGA[C/T]TTGATGTCTATAGTA	154214
rs504637	snp	A/G	0.067446	0.170804	intron-variant	RNF217	GRCh38.p7	6:125054151	TATGGAACTTCCATT[A/G]GGGATGTAGATGTCT	154214
rs506058	snp	A/C	0.492727	0.0598633	intron-variant	RNF217	GRCh38.p7	6:125044620	CTATATAATGAGAAT[A/C]ATAGGAACAAGTAAG	154214
rs508123	snp	A/G	0.109814	0.206997	intron-variant	RNF217	GRCh38.p7	6:125035247	atgttgaataggagt[A/G]gtgagagagggcatc	154214
rs508732	snp	A/G	0.49533	0.0480965	intron-variant	RNF217	GRCh38.p7	6:125044327	GCTAGAGTATTTTTC[A/G]TAAGTAGTGAACAAT	154214
rs510795	snp	C/T	0.110167	0.207236	intron-variant	RNF217	GRCh38.p7	6:125035520	ggtttgttgtctgca[C/T]gtttctcattgcttt	154214
rs511449	snp	C/T	0.0944967	0.195752	intron-variant	RNF217	GRCh38.p7	6:125078442	GTCATTTATTTGGCT[C/T]ATGGTTCTGGAGGCT	154214
rs512342	snp	C/G	0.47666	0.105476	intron-variant	RNF217	GRCh38.p7	6:125078546	CAAGCCCACGAGACA[C/G]AGAAAATGGGAGCCA	154214
rs518619	snp	C/T	0.0607341	0.163335	intron-variant	RNF217	GRCh38.p7	6:125072654	ATGAGGCAAAACTTA[C/T]TAGAACAAGTTTTTC	154214
rs520292	snp	A/T	0.486133	0.082104	intron-variant	RNF217	GRCh38.p7	6:125074044	ACCTCTCTGTAAGGC[A/T]GAAGCTTACCTGCCA	154214
rs520297	snp	C/G	0.486133	0.082104	intron-variant	RNF217	GRCh38.p7	6:125074048	CTCTGTAAGGCAGAA[C/G]CTTACCTGCCAAGTG	154214
rs521323	snp	A/C	0.222928	0.24853	intron-variant	RNF217	GRCh38.p7	6:125039516	GGAGACTTTAACACC[A/C]CATTTTCAATATTAG	154214
rs522187	snp	C/T	0.109814	0.206997	intron-variant	RNF217	GRCh38.p7	6:125036496	agatccaaaaggaat[C/T]gcaacaaaagccaaa	154214
rs522238	snp	G/T	0.415727	0.187175	intron-variant	RNF217	GRCh38.p7	6:125057362	AAACCCCATCTCTAC[G/T]AAAAATATAAAAATT	154214
rs523217	snp	A/G	0.0696718	0.173152	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125086097	GAACATATCCATAAG[A/G]TTGTACATTTGTTTT	154214
rs524695	snp	C/T	0.0700422	0.173537	intron-variant	RNF217	GRCh38.p7	6:125082720	TTAAAGAATGAAATA[C/T]TGAAGAAGTAAATAC	154214
rs524864	snp	C/T	0.100944	0.200705	intron-variant	RNF217	GRCh38.p7	6:125082777	TTGTATGTTCGTACA[C/T]TGCAAATAAATAAAC	154214
rs526790	snp	A/T	0.0700422	0.173537	intron-variant	RNF217	GRCh38.p7	6:125079888	TGTTACTAACCTAGG[A/T]ATAAGAGATAGTATG	154214
rs528201	snp	G/T	0.0611083	0.163768	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125092517	TCAAACTATTTTGAT[G/T]GTCATTGTACGAGCT	154214
rs529218	snp	C/T	0.0667028	0.170006	intron-variant	RNF217	GRCh38.p7	6:125059227	GACCTGGCTTTCTAA[C/T]AGAAGTGATGTCTAA	154214
rs529337	snp	A/G	0.0566069	0.158427	intron-variant	RNF217	GRCh38.p7	6:125065831	GCTGTTGGCTCAGTC[A/G]GTAGGCAAATCGTAA	154214
rs530999	snp	C/G	0.0599851	0.162463	intron-variant	RNF217	GRCh38.p7	6:125059402	AATGAGGCCTTCCCC[C/G]CTTTCTCTTGCCTTT	154214
rs537650	snp	C/T	0.478104	0.102316	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090503	AAAGAGAAAAAAATT[C/T]GAGTGTTTATCTGTT	154214
rs539463	snp	A/C	0.489201	0.0726845	intron-variant	RNF217	GRCh38.p7	6:125031884	gtatgtctttgtcaa[A/C]agtgtgaaaatggac	154214
rs539676	snp	G/T	0.478104	0.102316	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125090773	AGTTTAAAATGGACC[G/T]GGTTGAAAAGAGATT	154214
rs540840	snp	A/C	0.123452	0.215605	intron-variant	RNF217	GRCh38.p7	6:125071129	ACAACTTGAGGAGGA[A/C]AGGTACTATTTTCTT	154214
rs544426	snp	A/G	0.497933	0.032082	intron-variant	RNF217	GRCh38.p7	6:125071536	TGTGTGTGTGTGTGT[A/G]TATATCTTATTACAG	154214
rs545008	snp	C/T	0.0681886	0.171594	intron-variant	RNF217	GRCh38.p7	6:125050654	TTACACATTCTTATA[C/T]ATGGGAAACAGTTCT	154214
rs545124	snp	A/G	0.0700422	0.173537	intron-variant	RNF217	GRCh38.p7	6:125079792	AAATAGGGAAAAGAA[A/G]CAAAAAATTAAGTAT	154214
rs546893	snp	G/T	0.109814	0.206997	intron-variant	RNF217	GRCh38.p7	6:125036891	ttattatttattata[G/T]ttattatatattatt	154214
rs547130	snp	A/G	0.479095	0.100076	intron-variant	RNF217	GRCh38.p7	6:125071828	ATTTATGAGTGGCCA[A/G]TTTTATCTAATGGAT	154214
rs548862	snp	G/T	0.394354	0.204112	intron-variant	RNF217	GRCh38.p7	6:125050187	CAAGTGCAGACTGAA[G/T]AAATGATCCCCCTTT	154214
rs548865	snp	G/T	0.394171	0.204242	intron-variant	RNF217	GRCh38.p7	6:125050184	TTCCAAGTGCAGACT[G/T]AATAAATGATCCCCC	154214
rs552705	snp	C/T	0.156319	0.231784	intron-variant	RNF217	GRCh38.p7	6:125028989	AACTTCTTGATTTTG[C/T]TATTGGTCAACCAGG	154214
rs554975	snp	A/T	0.109814	0.206997	intron-variant	RNF217	GRCh38.p7	6:125040119	TTTGAAGGTTTTTTC[A/T]TGTCTCTATCTCCTT	154214
rs554999	snp	C/T	0.475437	0.108066	intron-variant	RNF217	GRCh38.p7	6:125066329	AGAGCAAAAGTTAGT[C/T]CTATGATGACCATAG	154214
rs555347	snp	G/T	0.0640965	0.167152	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087292	CAAAAATAAGAAAAT[G/T]TATGCCAAAAAACGT	154214
rs556142	snp	C/T	0.0592355	0.161582	intron-variant	RNF217	GRCh38.p7	6:125050478	TTTCTTTCTTATAAA[C/T]CCTCTGAGTAGAAAT	154214
rs556308	snp	A/G	0.478188	0.10213	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125087421	TCTCCCAACTATTGA[A/G]AGTGATCTTTCCCAT	154214
rs556784	snp	C/T	0.110167	0.207236	intron-variant	RNF217	GRCh38.p7	6:125033106	ctatttttCTTTTTT[C/T]TTCTTTTTTCAATAT	154214
rs560739	snp	A/G	0.481473	0.0944461	intron-variant	RNF217	GRCh38.p7	6:125050985	TACCCTTGAAAAAAC[A/G]TATAACACTCAGCTA	154214
rs561365	snp	A/C	0.125634	0.217214	intron-variant	RNF217	GRCh38.p7	6:125067020	TACGAGGGTTCATGG[A/C]GAAAGGACTCAACAC	154214
rs562841	snp	A/T	0.0562307	0.157967	intron-variant	RNF217	GRCh38.p7	6:125070008	ATCCCTTTCCCACTC[A/T]TACCTCCTATTCCTA	154214
rs564516	snp	C/T	0.499942	0.00539106	intron-variant, downstream-variant-500B	RNF217	GRCh38.p7	6:125081732	ACTGTGATTCATGTA[C/T]CTTATAAAGCATTAT	154214
rs565056	snp	A/G	0.0633504	0.166319	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091204	AAGGAAGAAGTTGGT[A/G]AATAAAAGCCAGGGA	154214
rs565968	snp	C/T	0.470521	0.117772	intron-variant	RNF217	GRCh38.p7	6:125060977	CTAACATTGCAAACA[C/T]TTCTCATATTACTGA	154214
rs567448	snp	C/T	0.498109	0.0306926	intron-variant	RNF217	GRCh38.p7	6:125053320	AGTAGCAGGAACTGC[C/T]TATGTTGATTGTAGG	154214
rs571846	snp	C/T	0.0532157	0.154195	intron-variant	RNF217	GRCh38.p7	6:125080418	TTGACAAACTTCCAA[C/T]AAATGGCTGTATTAG	154214
rs572110	snp	C/T	0.0667028	0.170006	intron-variant	RNF217	GRCh38.p7	6:125053644	GGTTGTTTCCTTACT[C/T]GACTTGATGAATTAT	154214
rs573804	snp	C/T	0.154993	0.231244	intron-variant	RNF217	GRCh38.p7	6:125049765	AACTATATTCTTTTT[C/T]ACTCCCCCATGCCCT	154214
rs575035	snp	A/C	0.124491	0.216211	intron-variant	RNF217	GRCh38.p7	6:125037955	AATTGAGCAATGAGG[A/C]CTGAGATTTGTACTT	154214
rs576419	snp	A/G	0.479583	0.0989539	intron-variant	RNF217	GRCh38.p7	6:125049480	CTTTTCAACCTTGGT[A/G]AATCCAACACCTCAA	154214
rs576558	snp	G/T	0.190583	0.249022	intron-variant	RNF217	GRCh38.p7	6:125047532	ATGTCTATCAATTTG[G/T]TGTAGGTAAGAAGAG	154214
rs577387	snp	A/G	0.124491	0.216211	intron-variant	RNF217	GRCh38.p7	6:125037953	TAAATTGAGCAATGA[A/G]GACTGAGATTTGTAC	154214
rs580862	snp	A/G	0.105569	0.204058	intron-variant	RNF217	GRCh38.p7	6:125041437	GTATTGTCTTTATAT[A/G]ATACAGACTTTTTAC	154214
rs723051	snp	C/T	0.0240643	0.107019	intron-variant	RNF217	GRCh38.p7	6:125079770	GGTTATGTGCAAGTA[C/T]AATTTAAAATAGGGA	154214
rs723052	snp	C/G	0.0240643	0.107019	intron-variant	RNF217	GRCh38.p7	6:125079869	AAATGATGTTTTAGA[C/G]CAATGTTACTAACCT	154214
rs911966	snp	A/C	0.470715	0.117409	intron-variant	RNF217	GRCh38.p7	6:125070947	GTATACATCTGCCCA[A/C]AAGTATTTGTCTCCA	154214
rs973396	snp	A/T	0.155987	0.23165	intron-variant	RNF217	GRCh38.p7	6:125026656	TAACTGTGATTCCCT[A/T]TTTTTTTTCTCAGAG	154214
rs990788	snp	C/T	0.470618	0.117591	intron-variant	RNF217	GRCh38.p7	6:125069547	cccatcaacagtgga[C/T]tggataaagaaaatg	154214
rs992970	snp	C/T	0.497776	0.0332724	intron-variant	RNF217	GRCh38.p7	6:125043859	TGTTAAAAGTATAAA[C/T]TGTTGCATAATTTTA	154214
rs1044723	snp	A/G	0.152001	0.229992	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091073	TCTTACACTTTTTAG[A/G]GCAATCAACTTATTT	154214
rs1044724	snp	A/C	0.152001	0.229992	utr-variant-3-prime, nc-transcript-variant	RNF217	GRCh38.p7	6:125091085	TAGAGCAATCAACTT[A/C]TTTCCAAATTATTAT	154214
rs1322632	snp	A/T	0.00636936	0.0560724	intron-variant	RNF217	GRCh38.p7	6:125080124	GAACAGACTGAGCTA[A/T]GTGCATAGGAGAAAA	154214

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