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
rs178746	snp	A/G	0.497803	0.033074	intron-variant	RNF212B	GRCh38.p7	14:23219216	caatctgaaagaaaa[A/G]gatgctaatgagcaa	100507650
rs178747	snp	A/G	0.486984	0.079614	intron-variant	RNF212B	GRCh38.p7	14:23219253	atcatcggaaggtac[A/G]aaactcactggtaag	100507650
rs178748	snp	A/G	0.243633	0.249919	intron-variant	RNF212B	GRCh38.p7	14:23219541	cagtggcaagatctc[A/G]gctcactgcaacctc	100507650
rs178749	snp	A/C	0	0	intron-variant	RNF212B	GRCh38.p7	14:23219669	tagagatggggtttc[A/C]ccatgttggtcaggc	100507650
rs178750	snp	C/T	0	0	intron-variant	RNF212B	GRCh38.p7	14:23220010	ccaacatggtgaaac[C/T]ccatctctaccaaaa	100507650
rs178751	snp	A/G	0	0	intron-variant	RNF212B	GRCh38.p7	14:23220855	acaaaaaacaaatac[A/G]caaaaaataaaagca	100507650
rs178752	snp	A/G	0.488606	0.0746142	intron-variant	RNF212B	GRCh38.p7	14:23221160	gggaggctgaggtgg[A/G]cagatcacttgaggt	100507650
rs178753	snp	C/T	0.461923	0.132621	intron-variant	RNF212B	GRCh38.p7	14:23222021	gtatagctataagtg[C/T]ctacatcaaaaagga	100507650
rs178754	snp	A/G	0.242488	0.249887	intron-variant	RNF212B	GRCh38.p7	14:23222721	gatgaatattgatgc[A/G]aaaatgctagtaaac	100507650
rs178755	snp	C/T	0.240765	0.249829	intron-variant	RNF212B	GRCh38.p7	14:23224206	ttcttatcaaaatac[C/T]gatgacattctccac	100507650
rs178756	snp	A/C	0.499722	0.0117779	intron-variant	RNF212B	GRCh38.p7	14:23226628	agagcgagactctgt[A/C]tcaaaaacaaaacaa	100507650
rs178757	snp	A/G	0.499673	0.0127754	intron-variant	RNF212B	GRCh38.p7	14:23227859	ccatcttagcccccc[A/G]aagtgctgggattac	100507650
rs178758	snp	A/G	0.247337	0.249986	intron-variant	RNF212B	GRCh38.p7	14:23229855	CTATATTCCCAATAA[A/G]ACATGCCCAACTGTC	100507650
rs178759	snp	A/G	0.499673	0.0127754	intron-variant	RNF212B	GRCh38.p7	14:23230649	acagagcgagactcc[A/G]tctcaaaaaaaaaaa	100507650
rs178761	snp	A/G	0.458545	0.137872	intron-variant	RNF212B	GRCh38.p7	14:23232847	ggggtgcctctgccc[A/G]gctgccccgtctggg	100507650
rs178762	snp	C/T	0.00874735	0.0655527	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236511	CAGAGTGAGACTCTG[C/T]TTCAAAAAACAACAA	100507650
rs178763	snp	G/T	0.287085	0.247234	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236714	aacaaaagctctttg[G/T]agggtcttcaataat	100507650
rs178764	snp	C/T	0.5	0	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236961	TTATTCTGTCTCTCt[C/T]ttttttttttttttt	100507650
rs178765	snp	A/G	0.43655	0.16643	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237529	TTTTTAAATTTTCCT[A/G]TTTCCGATTTTACGC	100507650
rs178766	snp	C/G	0.163236	0.234461	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237716	GGGGACAAATAAACA[C/G]TGTAACCTAATCCCA	100507650
rs178767	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237775	GGCTGCTGGGAAAAG[G/T]CTCCTACACCCCTCT	100507650
rs178768	snp	A/G	0.499234	0.0195537	intron-variant	RNF212B	GRCh38.p7	14:23239033	GAACAAACATTAAGT[A/G]ATTTTTCAAAGTCCA	100507650
rs178769	snp	C/T	0.499265	0.0191552	intron-variant	RNF212B	GRCh38.p7	14:23239178	TTATCATGCCTCAGC[C/T]TCCCAAGTAGCTGGG	100507650
rs178770	snp	C/T	0.499295	0.0187567	intron-variant	RNF212B	GRCh38.p7	14:23239351	AGGTGTGAGACACCA[C/T]GCTTGGCCTGATTCT	100507650
rs178771	snp	G/T	0.136166	0.22258	intron-variant	RNF212B	GRCh38.p7	14:23239560	GAAGTAGTTAAAAAA[G/T]AAATGGACGATTCAT	100507650
rs178772	snp	A/G	0.17138	0.237316	intron-variant	RNF212B	GRCh38.p7	14:23240631	GAATGGTCCTAAATT[A/G]TTTAGCAAATGATTT	100507650
rs178773	snp	C/T	0.172028	0.23753	intron-variant	RNF212B	GRCh38.p7	14:23242036	gcagtgagccaagat[C/T]gtgccactgcactcc	100507650
rs178774	snp	A/G	0	0	intron-variant	RNF212B	GRCh38.p7	14:23242098	aaaaaaaaaaaaaaa[A/G]aaaaaaaaagaaaAG	100507650
rs178775	snp	A/G	0.17461	0.238362	intron-variant	RNF212B	GRCh38.p7	14:23243418	AAAGAAAAGAAgacc[A/G]ggcgtggtggctcag	100507650
rs178776	snp	C/T	0.499203	0.0199521	intron-variant	RNF212B	GRCh38.p7	14:23243540	gtctctactaaaata[C/T]aaaaaattagccagg	100507650
rs178777	snp	C/G	0.438666	0.164028	intron-variant	RNF212B	GRCh38.p7	14:23243911	aggaaaccctcgtct[C/G]tactaaaaatacaaa	100507650
rs178778	snp	C/T	0.49917	0.0203505	intron-variant	RNF212B	GRCh38.p7	14:23245039	ACTTTGGTTTTTTTC[C/T]TTCTACTCCCCATTT	100507650
rs729531	snp	A/G	0.0850919	0.187897	intron-variant	RNF212B	GRCh38.p7	14:23187209	TCTAAATCCATATTT[A/G]TAAGAAAACGGCCTT	100507650
rs742874	snp	C/G	0.175897	0.238765	intron-variant	RNF212B	GRCh38.p7	14:23249460	TGAGGTGGGAGAATT[C/G]CTTGATCCCAAGAGG	100507650
rs755575	snp	C/T	0.445592	0.155704	intron-variant	RNF212B	GRCh38.p7	14:23249459	CTGAGGTGGGAGAAT[C/T]GCTTGATCCCAAGAG	100507650
rs761875	snp	G/T	0.488846	0.0738428	intron-variant	RNF212B	GRCh38.p7	14:23187672	AGATTTGGGTCCTTT[G/T]TTGGTAACCTCAGAC	100507650
rs977870	snp	G/T	0.497502	0.035255	intron-variant	RNF212B	GRCh38.p7	14:23255938	TCAGGCAAAATCACT[G/T]CTTCTTTAATACTCC	100507650
rs977871	snp	C/T	0.495174	0.0488838	intron-variant	RNF212B	GRCh38.p7	14:23256030	GTAGACAAAGTAGGT[C/T]TGCTTAGGCCTGGCA	100507650
rs1055375	snp	A/G	0.0329836	0.124112	utr-variant-3-prime, downstream-variant-500B	RNF212B	GRCh38.p7	14:23273087	GTCTTACAAAAGGCT[A/G]GTGCTTCAGGAAGAT	100507650
rs1569952	snp	C/T	0.478768	0.100824	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184262	GCTCACGTGATCCTC[C/T]CCTGTCAGCCTCCCA	100507650
rs1569953	snp	A/G	0	0	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184149	AAGAACCTTTTTCCC[A/G]TTGTTAATTCCTTCC	100507650
rs1884543	snp	A/C	0.031825	0.122064	intron-variant	RNF212B	GRCh38.p7	14:23188456	AAAAAAAAAAACCCT[A/C]ATCTTTGTCAAACAT	100507650
rs1884544	snp	A/G	0.118933	0.212888	intron-variant	RNF212B	GRCh38.p7	14:23188392	ATTTAAGTATTCAAA[A/G]CTGGAGTCACTTAAA	100507650
rs1955560	snp	A/G	0.25912	0.249834	intron-variant	RNF212B	GRCh38.p7	14:23252548	ggggtttaatcataa[A/G]acagctgaacaagga	100507650
rs1955561	snp	A/G	0.136847	0.222927	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23259581	CAAGATGGAGTCCTT[A/G]ATAAAAATTTTTAGA	100507650
rs1963151	snp	A/G	0.46974	0.119223	intron-variant	RNF212B	GRCh38.p7	14:23263529	TCTCGGCTTAAGGGA[A/G]TTAAGTTTATGCTGA	100507650
rs2064482	snp	C/T	0.353803	0.227431	intron-variant	RNF212B	GRCh38.p7	14:23240106	ATGTATATATATATA[C/T]ACACACACACATTTA	100507650
rs2064483	snp	A/G	0.475525	0.107882	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260541	TTCCTCCTACTGGGA[A/G]TCTTAGCAACCATGA	100507650
rs2064750	snp	A/C	0.177503	0.239258	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213702	TTTGGCATGCAGTCA[A/C]CCTGTTTAGGTAGAG	100507650
rs2064751	snp	A/C	0.177503	0.239258	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213701	TTGGCATGCAGTCAC[A/C]CTGTTTAGGTAGAGC	100507650
rs2064752	snp	C/G	0.177503	0.239258	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213693	CAGTCACCCTGTTTA[C/G]GTAGAGCACACAGTT	100507650
rs2064753	snp	A/G	0.178465	0.239547	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213490	ATACTTCTTCTTTCC[A/G]CCTCATGACTCCTGG	100507650
rs2064754	snp	A/C	0.178144	0.239451	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213426	GATCAAATTGGGAAA[A/C]ATTGACTTCTTAACA	100507650
rs2092706	snp	A/G	0.0267878	0.112589	intron-variant	RNF212B	GRCh38.p7	14:23243907	CATGAGGAAACCCTC[A/G]TCTCTACTAAAAATA	100507650
rs2092708	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23222040	catcaaaaaggaaga[A/C]gaacttcaaacaaat	100507650
rs2092709	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23222103	caagagcaaaccaaa[A/C]ccaaaattaggagaa	100507650
rs2092710	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23222132	aaaaaaagcaaaaat[A/C]tggatcagagcagaa	100507650
rs2092711	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23222136	aaagcaaaaatatgg[A/C]tcagagcagaaataa	100507650
rs2144037	snp	A/G	0.198634	0.244666	intron-variant	RNF212B	GRCh38.p7	14:23218331	caagattgcacctct[A/G]cactatagcctgggt	100507650
rs2144038	snp	C/T	0.313741	0.241738	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23259979	CTTATTATTATTTTC[C/T]CTCTTACTTTTCTCA	100507650
rs2144039	snp	A/G	0.475525	0.107882	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260193	TGACCTACCAGTTGG[A/G]AAGCTCTCTTATAGA	100507650
rs2144828	snp	A/T	0.463851	0.12949	intron-variant	RNF212B	GRCh38.p7	14:23218375	TCTTTTTATTTATTT[A/T]TTTTTTTGAGATAGA	100507650
rs2144829	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23217442	ggccaaggcccttct[C/T]ttcagggcagcgagt	100507650
rs2179931	snp	A/G	0.349671	0.229272	intron-variant	RNF212B	GRCh38.p7	14:23265184	AAAATAAAGATTTGA[A/G]TGATAGAAAGTCATT	100507650
rs2331938	snp	C/T	0.029116	0.117091	intron-variant	RNF212B	GRCh38.p7	14:23186913	TGGTCAAAGCCTCAA[C/T]TTCTTTCACCTGAGG	100507650
rs2331939	snp	A/G	0.0744748	0.178019	utr-variant-5-prime, nc-transcript-variant	RNF212B	GRCh38.p7	14:23193372	agggaataagtaaag[A/G]aggaagaagaccctg	100507650
rs2331940	snp	A/G	0.408017	0.193729	intron-variant	RNF212B	GRCh38.p7	14:23194476	ggcgcagtgacacac[A/G]cctataatcccagca	100507650
rs2331941	snp	A/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23205300	tttttctcttttttt[A/T]aaaaaaaggacaccc	100507650
rs2331942	snp	C/G	0.49975	0.0111793	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23205479	tattttattttaatt[C/G]tttacctagattatt	100507650
rs2331943	snp	C/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213689	TAGGAACTGTGTGCT[C/G]TACCTAAACAGGGTG	100507650
rs2331944	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213690	AGGAACTGTGTGCTC[C/T]ACCTAAACAGGGTGA	100507650
rs2331945	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213695	CTGTGTGCTCTACCT[A/G]AACAGGGTGACTGCA	100507650
rs2331946	snp	A/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213697	GTGTGCTCTACCTAA[A/T]CAGGGTGACTGCATG	100507650
rs2331947	snp	G/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213700	TGCTCTACCTAAACA[G/T]GGTGACTGCATGCCA	100507650
rs2331948	snp	C/T	0.26818	0.249338	intron-variant	RNF212B	GRCh38.p7	14:23218174	gagatcgagaccctc[C/T]tggctaacacggtga	100507650
rs2474013	snp	C/T	0.00398564	0.0444627	intron-variant	RNF212B	GRCh38.p7	14:23227850	gtgattcacccacct[C/T]agccccccgaagtgc	100507650
rs2474514	snp	A/G	0.249038	0.249998	intron-variant	RNF212B	GRCh38.p7	14:23227847	CTTCGGGGGGCTGAG[A/G]TGGGTGAATCACCTG	100507650
rs2877514	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23271263	gaccaatatggtaaa[A/C]ccccgtctctctcta	100507650
rs2877535	snp	A/G	0.482979	0.0906686	intron-variant	RNF212B	GRCh38.p7	14:23194524	gggcagatcatctga[A/G]ctcaggagtttgaga	100507650
rs2877536	snp	A/G	0.496842	0.0396107	intron-variant	RNF212B	GRCh38.p7	14:23217262	GGCAGTGGTGGGGGG[A/G]GGGCTCCTCTGCCTG	100507650
rs3045528	in-del	-/AAAAAAAAA	0	0	intron-variant	RNF212B	GRCh38.p7	14:23193110	AAAAAAAAAAAAAAA[-/AAAAAAAAA]GAATGTTACCAGAAT	100507650
rs3045551	in-del	-/CCT			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213692	GAACTGTGTGCTCTA[-/CCT]AAACAGGGTGACTGC	100507650
rs3811180	snp	A/G	0.421368	0.182025	intron-variant	RNF212B	GRCh38.p7	14:23264516	ATATATTGTTCTACT[A/G]CAGTGGGCATACTAG	100507650
rs4375573	snp	C/T	0.352287	0.228117	intron-variant	RNF212B	GRCh38.p7	14:23271029	AGGAAAAACCACATT[C/T]ACTTCTCCAGAGACC	100507650
rs4619311	snp	C/T	0.158632	0.232706	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209263	GTGGGTTTTGGCCGG[C/T]TCCTTTACCGCAACC	100507650
rs4981460	snp	A/C	0.3744	0.216852	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23212467	AATAATGGGGTTTGA[A/C]AAGTTTGTAGAATAC	100507650
rs4981462	snp	C/T	0.236144	0.249616	intron-variant	RNF212B	GRCh38.p7	14:23216669	CAGATTGCTTGAGCT[C/T]AGGAGTTCAAGACAA	100507650
rs4982739	snp	C/T	0.0267878	0.112589	intron-variant	RNF212B	GRCh38.p7	14:23189848	cttcccttgatgctc[C/T]attcctttcagctac	100507650
rs4982740	snp	C/T	0.483272	0.0899109	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195437	ACCATATCTCTTGTC[C/T]ACCTCTAAGGCTTCG	100507650
rs4982745	snp	C/T	0.0685596	0.171987	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237422	ggcgtgagccaccgc[C/T]cctggccAAAAATTT	100507650
rs4982747	snp	C/G	0.381697	0.212499	intron-variant	RNF212B	GRCh38.p7	14:23272380	agcggagatgcacca[C/G]tgcactccagcctgg	100507650
rs5807213	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23240047	CTCAAAAAAAAAAAA[-/A]TCTCACCACTGTCTG	100507650
rs5807215	snp	A/T	0.42357	0.179927	intron-variant	RNF212B	GRCh38.p7	14:23264828	ACAAGGTTTTTTTTT[A/T]TTTTTTTGGTGAGAT	100507650
rs6573018	snp	A/G	0.0310518	0.120672	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184075	GGAGAGAACGTTGAA[A/G]GGACATCATCTTCGA	100507650
rs6573034	snp	C/G	0.0236746	0.106192	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200384	AGGCTAGAGTGCAAT[C/G]GCATGATCTTGGCCC	100507650
rs6573044	snp	A/G	0.00636936	0.0560724	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206222	TGGGATTATAGGTGC[A/G]CACCACCATGGCCAG	100507650
rs6573045	snp	A/G	0.175254	0.238565	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213140	ACACAGTGAAACCCC[A/G]TCTCTACTAAAAAAT	100507650
rs6573046	snp	C/T	0.227664	0.249	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213169	ATACAAAAAATTAGC[C/T]GGGCGTGGTGGCAGG	100507650
rs6573047	snp	A/G	0.16846	0.236329	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213176	AAATTAGCCGGGCGT[A/G]GTGGCAGGCGCCTGT	100507650
rs6573048	snp	A/G	0.174288	0.23826	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213182	GCCGGGCGTGGTGGC[A/G]GGCGCCTGTAGTCCC	100507650

Full records

It may take some time, please wait.