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
rs8357	snp	C/G	0.104504	0.2033	utr-variant-3-prime	PLCG2	GRCh38.p7	16:81958259	TTGGCCTCTCATGTT[C/G]CAAACCTCATTGAAT	5336
rs1071644	snp	C/T	0.49473	0.051063	synonymous-codon	PLCG2	GRCh38.p7	16:81937798	ATTGTTTTCTCTCAA[C/T]GGGCGCACGGGCTAC	5336
rs1130733	snp	A/G	0	0	missense	PLCG2	GRCh38.p7	16:81938886	GTGGAGCCGAGTATG[A/G]CAACAACAAGTTCAA	5336
rs1130756	snp	C/T	0	0	utr-variant-3-prime	PLCG2	GRCh38.p7	16:81958108	TCTGTGACATCTTTT[C/T]TTCAAGCCTGCCATC	5336
rs1137750	snp	C/T	0.0551013	0.156571	intron-variant	PLCG2	GRCh38.p7	16:81935169	GTCAACATCAGGGTG[C/T]CAGCAGGGCTGTGCT	5336
rs1143685	snp	C/T	0.398955	0.200779	synonymous-codon	PLCG2	GRCh38.p7	16:81786163	CTGGAGCAAGACCGC[C/T]GACAAGATCGAGGGC	5336
rs1143686	snp	A/G	0.39898	0.200773	synonymous-codon	PLCG2	GRCh38.p7	16:81854547	CTGCTTCACCATCCT[A/G]TATGGCACTCAGTTC	5336
rs1143687	snp	C/T	0.118966	0.212909	missense	PLCG2	GRCh38.p7	16:81889208	AACAAAGTCCGTGAG[C/T]GGATGACAAAGTTCA	5336
rs1143688	snp	C/T	0.48582	0.0830003	synonymous-codon	PLCG2	GRCh38.p7	16:81895883	CAAGATCAAGTTTGA[C/T]GACGTCGTGCAGGCC	5336
rs1143689	snp	C/T	0.339015	0.233625	synonymous-codon	PLCG2	GRCh38.p7	16:81907714	CTACTGCGCCATTGC[C/T]GATGCCAAGCTGTCC	5336
rs1143690	snp	C/T	0.0198289	0.097577	synonymous-codon	PLCG2	GRCh38.p7	16:81936242	CAGACAGAAGCCCGT[C/T]GACCTCCTGAAGTAC	5336
rs2965754	snp	A/G			intron-variant	PLCG2	GRCh38.p7	16:81933609	TTGAGTagcctgggc[A/G]acagagtgagactct	5336
rs2966242	snp	A/C			intron-variant	PLCG2	GRCh38.p7	16:81933576	ctcaaaaaaaaaaaa[A/C]aaaaaaCAGCATGAC	5336
rs3088217	snp	C/G	0.499933	0.00579035	utr-variant-3-prime	PLCG2	GRCh38.p7	16:81962346	TGTATAATTCCAAAT[C/G]TAATTATTAACTTTT	5336
rs3189935	snp	C/G	0	0	missense	PLCG2	GRCh38.p7	16:81931553	ATCCTGGAGCCCAAG[C/G]AGCAGGGCGATCCTC	5336
rs3813009	snp	C/G	0.168135	0.236216	intron-variant	PLCG2	GRCh38.p7	16:81927353	GATTGAGTTGTTGTG[C/G]GTGAGTTGCTGTGAC	5336
rs3813010	snp	C/T	0.426354	0.177198	intron-variant	PLCG2	GRCh38.p7	16:81927397	TTTAATCAGGTTGTG[C/T]TGGGCTTGGAAGGAT	5336
rs3813011	snp	A/G	0.286303	0.24735	intron-variant	PLCG2	GRCh38.p7	16:81932957	CTCTGAGGCACAGGG[A/G]GGTGCCACGACCCTG	5336
rs3893311	snp	C/T	0.0637235	0.166737	intron-variant	PLCG2	GRCh38.p7	16:81867962	cctgtaatcccagca[C/T]tttgggaggctgagg	5336
rs3922849	snp	C/T	0.49941	0.0171624	intron-variant	PLCG2	GRCh38.p7	16:81921572	TTTTTGGCTCGCTGA[C/T]AGAGCCTGTGGTGTT	5336
rs3922850	snp	A/G	0.451608	0.147832	intron-variant	PLCG2	GRCh38.p7	16:81921633	TGCAGTGCAAATGCT[A/G]TCTCATATTCCCACC	5336
rs3923153	snp	C/T	0.304438	0.244001	intron-variant	PLCG2	GRCh38.p7	16:81930399	CTCATGGCTGCATTC[C/T]TCAGTCTCCACATTT	5336
rs3924349	snp	G/T	0.408188	0.193589	intron-variant	PLCG2	GRCh38.p7	16:81795876	GGCCCCCTCCCACCT[G/T]CTATTGAACAGAATT	5336
rs3934954	snp	A/G	0.41325	0.18934	intron-variant	PLCG2	GRCh38.p7	16:81936754	CATTTACATGCTGGC[A/G]TAACTAACATACACA	5336
rs3934955	snp	A/C	0.498253	0.0295011	intron-variant	PLCG2	GRCh38.p7	16:81936761	ATGCTGGCATAACTA[A/C]CATACACAAACTTCT	5336
rs3934956	snp	C/T	0.499104	0.0211472	intron-variant	PLCG2	GRCh38.p7	16:81936802	TGATCGCATAAATCA[C/T]GGGGCTTTGTGCTTT	5336
rs3934957	snp	C/G	0.49706	0.0382258	intron-variant	PLCG2	GRCh38.p7	16:81936866	CTATTCATCAGTAGC[C/G]TCCTTTACATTCTTT	5336
rs3934985	snp	A/G	0.499609	0.0139722	intron-variant	PLCG2	GRCh38.p7	16:81867728	CCTGGGTGACAGAGC[A/G]AGACTCCATCTCCAA	5336
rs3934986	snp	G/T	0.130008	0.219321	intron-variant	PLCG2	GRCh38.p7	16:81867991	GCAAGggccaggcac[G/T]gtggtggctcacgcc	5336
rs3935625	snp	A/C/G	6.73991e-05	0.00580474	missense	PLCG2	GRCh38.p7	16:81905422	ACATCCACATCGCCT[A/C/G]GGGGGCCCAGCTTCT	5336
rs3935647	snp	C/T	0.488241	0.0757703	upstream-variant-2KB	PLCG2	GRCh38.p7	16:81779166	GGAGCGCACCCCGAG[C/T]GCAGCGTCCCCGCGC	5336
rs3935743	snp	A/C	0.25801	0.249872	intron-variant	PLCG2	GRCh38.p7	16:81876375	GTACTTAGGCTGTAG[A/C]AACCATTTGGTTCTG	5336
rs3935744	snp	C/T	0.330947	0.236533	intron-variant	PLCG2	GRCh38.p7	16:81876232	AGTTCAAGCCTAGCC[C/T]GGGTAACATGGTGAA	5336
rs3935876	snp	C/T	0.48435	0.0870631	intron-variant	PLCG2	GRCh38.p7	16:81867190	GGCTGGGCAGTGACG[C/T]GCTACTTCCTTCCGC	5336
rs3935877	snp	C/T	0.276267	0.248616	intron-variant	PLCG2	GRCh38.p7	16:81867248	TACAGGGAAACTAGG[C/T]GGTTTTCTCCTGCAA	5336
rs3936112	snp	A/G	0.358728	0.225118	intron-variant	PLCG2	GRCh38.p7	16:81937333	CACTGCTCCCTAAAT[A/G]AGGGAAAAACTGGTT	5336
rs4072681	snp	G/T	0.49089	0.0668743	intron-variant	PLCG2	GRCh38.p7	16:81853886	ATCCAGAACCCCTGT[G/T]ACCATCCCCAACGCT	5336
rs4072682	snp	C/T	0.405255	0.195948	intron-variant	PLCG2	GRCh38.p7	16:81853898	TGTTACCATCCCCAA[C/T]GCTGGGGTTGGCCTC	5336
rs4072683	snp	C/T	0.314057	0.241654	intron-variant	PLCG2	GRCh38.p7	16:81853936	TATTTTTAATTTGAA[C/T]CAGTTAGTGCCTTCA	5336
rs4072828	snp	C/G	0.398657	0.201013	intron-variant	PLCG2	GRCh38.p7	16:81854632	ACTTCTTCAGGAAGA[C/G]ACTAAGGCACAGGGA	5336
rs4072830	snp	G/T	0.362523	0.223246	intron-variant	PLCG2	GRCh38.p7	16:81854352	CAGGCACAGCCTGGC[G/T]CCTTCCTTCCCCAAC	5336
rs4072831	snp	C/T	0.334182	0.235401	intron-variant	PLCG2	GRCh38.p7	16:81854298	CGTCTGGACTCAGTG[C/T]CCCCTCCTTCTGGAA	5336
rs4073295	snp	A/G	0.499995	0.00159744	intron-variant	PLCG2	GRCh38.p7	16:81836417	GGATCTTGGCTTCTC[A/G]TTTCATCCTTCCCTT	5336
rs4073313	snp	C/G	0.178465	0.239547	intron-variant	PLCG2	GRCh38.p7	16:81780108	ATTAGGGTACCAAGA[C/G]AGCCCCGCCCCACCG	5336
rs4073314	snp	A/C			intron-variant	PLCG2	GRCh38.p7	16:81780583	TCATTAGGTGACTTA[A/C]ACATCAGTGAGGCTC	5336
rs4073828	snp	A/G	0.496999	0.0386216	intron-variant	PLCG2	GRCh38.p7	16:81936890	ATTCTTTTTATAGCC[A/G]CATCGGATTCCACAG	5336
rs4073829	snp	C/G	0.388587	0.208071	intron-variant	PLCG2	GRCh38.p7	16:81936583	AGGCTGCTTGGCTTA[C/G]GCAGGCTTCGTGATT	5336
rs4074445	snp	G/T	0.108048	0.20579	intron-variant	PLCG2	GRCh38.p7	16:81856277	aacacctcatggAAC[G/T]ATGAAGCCTCTCCTT	5336
rs4076360	snp	C/T	0.464523	0.128375	intron-variant	PLCG2	GRCh38.p7	16:81893289	CAGGCACAGAACAGA[C/T]ATTCAACAACTGTTG	5336
rs4077748	snp	C/G	0.10237	0.201756	intron-variant	PLCG2	GRCh38.p7	16:81814624	cactgcaacctccac[C/G]tcccgggttcaagtg	5336
rs4077797	snp	C/T	0.367708	0.220556	intron-variant	PLCG2	GRCh38.p7	16:81865664	GGGGCCCTGGCCTCT[C/T]CCTTGCTCCCAGGAT	5336
rs4077853	snp	C/T	0.463126	0.13068	intron-variant	PLCG2	GRCh38.p7	16:81937365	GAAGCACAAATAGTT[C/T]CCAGAAAAGAAAATG	5336
rs4078270	snp	A/C	0.223225	0.248562	intron-variant	PLCG2	GRCh38.p7	16:81942075	AGAAATCTGTTACAG[A/C]GTCAAGGCTAGGAAC	5336
rs4133124	snp	A/C	0.493703	0.0557558	intron-variant	PLCG2	GRCh38.p7	16:81885924	CTCAAACTTAGTCTC[A/C]GGTTGGGCAAATAAG	5336
rs4133125	snp	G/T	0.25045	0.25	intron-variant	PLCG2	GRCh38.p7	16:81885861	ACTAGGAAGGCATGA[G/T]GATTACAACACGCAT	5336
rs4243210	snp	C/T	0.308661	0.24302	intron-variant	PLCG2	GRCh38.p7	16:81785343	CAGTCTACCCAGAGC[C/T]ACACAGTCAGCAGGA	5336
rs4243211	snp	A/G	0.469049	0.120489	intron-variant	PLCG2	GRCh38.p7	16:81786911	TCCCTAAACCATCCT[A/G]CTGAGGCAAGCTCAT	5336
rs4243212	snp	A/T	0.00398564	0.0444627	intron-variant	PLCG2	GRCh38.p7	16:81815668	AGCATGGGAAAATCC[A/T]GCCTGATTTTTTCCA	5336
rs4243213	snp	C/T	0.00398564	0.0444627	intron-variant	PLCG2	GRCh38.p7	16:81815712	TGGTGGCTTCTTCGA[C/T]TCTCGCGGTCTTCTT	5336
rs4243214	snp	C/G	0.00478085	0.0486577	intron-variant	PLCG2	GRCh38.p7	16:81815770	CGCTATAATTGAGCA[C/G]TCTTAAATgaccaga	5336
rs4243215	snp	A/G	0.227369	0.248974	intron-variant	PLCG2	GRCh38.p7	16:81815777	ATTGAGCAGTCTTAA[A/G]Tgaccagacacagtg	5336
rs4243216	snp	A/G	0.41023	0.191902	intron-variant	PLCG2	GRCh38.p7	16:81817172	GGACAGGAAGAGCGC[A/G]CATGATGGGTGGTCA	5336
rs4243217	snp	A/G	0.00398564	0.0444627	intron-variant	PLCG2	GRCh38.p7	16:81817189	ATGATGGGTGGTCAG[A/G]AAAGGCCTCTCTGAG	5336
rs4243218	snp	C/T	0.482905	0.0908579	intron-variant	PLCG2	GRCh38.p7	16:81867023	TCTGTCTGTGAAAGC[C/T]GTGGGTGCTGTCCCT	5336
rs4243219	snp	C/G	0.425432	0.178112	intron-variant	PLCG2	GRCh38.p7	16:81875784	AAGAAAATTGAGAAG[C/G]CTGCTAACGTATCTC	5336
rs4243220	snp	A/G	0.273856	0.248859	intron-variant	PLCG2	GRCh38.p7	16:81903173	gcaGTAGGCAGAGAA[A/G]GGGGATGTCCTTCCA	5336
rs4243222	snp	C/T	0.499974	0.00359416	intron-variant	PLCG2	GRCh38.p7	16:81912818	GCTCACCTGCAGTGC[C/T]CTGCCCCCCCAGCAT	5336
rs4243223	snp	G/T	0.499968	0.00399348	intron-variant	PLCG2	GRCh38.p7	16:81912866	ACCACAGCAAAAGCC[G/T]CTGCGAGAATGTGCG	5336
rs4243224	snp	G/T	0.424193	0.179323	intron-variant	PLCG2	GRCh38.p7	16:81927986	GTGCAGGGGGTGGGG[G/T]TTGGGGTGGTGCAGG	5336
rs4243225	snp	G/T	0.253264	0.249979	intron-variant	PLCG2	GRCh38.p7	16:81948043	CCCTAATTCACTTAT[G/T]CTCCTACTAACGGAG	5336
rs4243226	snp	A/G	0.335101	0.23507	utr-variant-3-prime	PLCG2	GRCh38.p7	16:81960369	ACTAGTAACAGGCAC[A/G]TTCTGAAAGATGGAA	5336
rs4254322	snp	A/G	0.304188	0.244057	intron-variant	PLCG2	GRCh38.p7	16:81779948	GATGCCCGCTCCGCA[A/G]CTGTCTGCGTAATTA	5336
rs4258606	snp	A/G	0.0345262	0.126772	intron-variant	PLCG2	GRCh38.p7	16:81795956	TGCTAGAAGAACAGG[A/G]CCTAAGTTGGGGGGC	5336
rs4258607	snp	C/T	0.428635	0.174898	intron-variant	PLCG2	GRCh38.p7	16:81833805	CTCCTGCCTTGGCCT[C/T]CCAAAGTGGTGGGGT	5336
rs4258608	snp	A/G	0.466204	0.125522	intron-variant	PLCG2	GRCh38.p7	16:81937977	CGATGCTGTCTTGAG[A/G]GCAGGGAACCCATGT	5336
rs4264387	snp	C/T	0.341909	0.232492	intron-variant	PLCG2	GRCh38.p7	16:81905632	CAAGTGAGTTTTTGC[C/T]ATGTGAATTTACCTT	5336
rs4265800	snp	A/T	0.397994	0.201489	intron-variant	PLCG2	GRCh38.p7	16:81798627	TACAAGTTGTGCTGG[A/T]GGCCAGGGGTAGGCG	5336
rs4273032	snp	A/G	0.40157	0.198813	upstream-variant-2KB	PLCG2	GRCh38.p7	16:81778631	CTGACTCCCTTTGGG[A/G]CTGGCACTATGTTGA	5336
rs4274427	snp	A/C	0.257732	0.24988	intron-variant	PLCG2	GRCh38.p7	16:81787666	TGCAAGCACCACTCC[A/C]ATCAAAAGTAGAACC	5336
rs4274430	snp	A/G	0.499187	0.0201513	intron-variant	PLCG2	GRCh38.p7	16:81799994	GACTGCCTGGGTTCA[A/G]ATCTTGGCTATGCCA	5336
rs4281703	snp	C/G	0.377977	0.21476	intron-variant	PLCG2	GRCh38.p7	16:81784835	GTCCCTGGTGGTTCA[C/G]CTCCAGGGCCTGGGG	5336
rs4281704	snp	C/G	0.342806	0.232136	intron-variant	PLCG2	GRCh38.p7	16:81784854	CAGGGCCTGGGGAGC[C/G]CCTTCACTCTAAGTC	5336
rs4281705	snp	A/G	0.490997	0.0664859	intron-variant	PLCG2	GRCh38.p7	16:81784918	TTTGGGAGGCAGAAT[A/G]AGGGAATGGTACAGA	5336
rs4284633	snp	A/G	0.140242	0.224618	intron-variant	PLCG2	GRCh38.p7	16:81947135	ACAACCGGAAACATT[A/G]TAAATAATTTAAGTG	5336
rs4286102	snp	C/T	0.272511	0.248984	intron-variant	PLCG2	GRCh38.p7	16:81904358	aaatctggatctgac[C/T]ccctatcctgagctc	5336
rs4286103	snp	C/T	0.435694	0.167385	utr-variant-3-prime	PLCG2	GRCh38.p7	16:81959301	CCTCCTCTTGTTACC[C/T]GAAATGCTGGGCTTA	5336
rs4288988	snp	G/T	0.27008	0.249192	intron-variant	PLCG2	GRCh38.p7	16:81787677	ctccaatcaaaagta[G/T]aacctttatatcacc	5336
rs4293371	snp	C/G	0.227664	0.249	intron-variant	PLCG2	GRCh38.p7	16:81793248	AGGAGCTGGTTGTCT[C/G]TGAATGTCGGGAGGG	5336
rs4294811	snp	A/G	0.404815	0.196297	intron-variant	PLCG2	GRCh38.p7	16:81786215	GGGGCAGTGTGGCCC[A/G]TCCTCTGGGGCCCTG	5336
rs4305012	snp	A/G	0.232067	0.249356	intron-variant	PLCG2	GRCh38.p7	16:81904109	TTTGCTGAGGAAATT[A/G]TTCAAGGCCAAGGTG	5336
rs4306503	snp	C/T	0.123798	0.215808	intron-variant	PLCG2	GRCh38.p7	16:81905861	gatgggatttagtcg[C/T]gttgcccagggtgat	5336
rs4306504	snp	C/T	0.498415	0.0281103	intron-variant	PLCG2	GRCh38.p7	16:81913109	AGGCCTGTGATGATA[C/T]AGATCTGGTTTCCTC	5336
rs4312298	snp	G/T	0.466308	0.125343	intron-variant	PLCG2	GRCh38.p7	16:81947571	GGTAAACAGCCTCAA[G/T]GCAGACTTTTCTGAG	5336
rs4312300	snp	C/G	0.489259	0.0724914	upstream-variant-2KB	PLCG2	GRCh38.p7	16:81778495	AAAGAGCATAGGAAG[C/G]GTTTGAATCAGATAG	5336
rs4313806	snp	A/C	0.498253	0.0295011	intron-variant	PLCG2	GRCh38.p7	16:81916622	AAAGTCTACCCTCAG[A/C]AATTTTCAAGAATAC	5336
rs4319763	snp	C/G	0.210301	0.246828	intron-variant	PLCG2	GRCh38.p7	16:81779792	GCCGTCTCTCTTGAC[C/G]GCCCTTGTGCCCAGA	5336
rs4322655	snp	C/G	0.385932	0.209815	intron-variant	PLCG2	GRCh38.p7	16:81822938	AAGCAGGTTTTCCCT[C/G]GGAGCCTCCAGAAGG	5336
rs4322656	snp	A/G	0.00398564	0.0444627	intron-variant	PLCG2	GRCh38.p7	16:81813579	ttTCTATAACAGTGT[A/G]aaaacacaggagctt	5336
rs4325546	snp	C/T	0.468949	0.12067	intron-variant	PLCG2	GRCh38.p7	16:81840216	GCTGCCTGGAGAGCA[C/T]GCTTAGAATTGAGCC	5336
rs4334287	snp	G/T	0.00953873	0.0683987	intron-variant	PLCG2	GRCh38.p7	16:81867750	TCACCCAGGCTGGAG[G/T]GCAGTGGCGTGATCT	5336

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