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
rs6759	snp	C/T	0.499999	0.000523047	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226882036	AGAGGATGGAGAGAA[C/T]ACTGCCCAGTGGGTA	5664
rs7961	snp	C/T	0.197703	0.244469	utr-variant-5-prime, nc-transcript-variant	PSEN2	GRCh38.p7	1:226875528	CCGGGATTCAGACCT[C/T]TCTGCGGCCCCAAGT	5664
rs7962	snp	C/G	0.0158469	0.0875917	utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226896066	GGAAGTGGCTTAATA[C/G]TAATATCAATAAATA	5664
rs8383	snp	C/T	0.495174	0.0488838	utr-variant-3-prime, downstream-variant-500B, intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226895849	AAGGTCAGATTAGGG[C/T]GGGGAGAAGAGCATC	5664
rs11405	snp	C/T	0.364439	0.22227	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226881976	GTCCCTAATGTCGGC[C/T]GAGAGCCCCACGCCG	5664
rs732479	snp	A/G	0.228547	0.249078	intron-variant	PSEN2	GRCh38.p7	1:226877777	TCTGGTGAGGAGGCC[A/G]CATGTATGAATGACG	5664
rs743601	snp	C/T	0.399253	0.200558	intron-variant	PSEN2	GRCh38.p7	1:226892465	ACGGTGCCTGCCTAA[C/T]ACCCAATGCCAGCCC	5664
rs743602	snp	C/T	0.255503	0.249939	intron-variant	PSEN2	GRCh38.p7	1:226892584	CCTGGTGACAGTGGC[C/T]TGGCATACAGGACTC	5664
rs1046240	snp	C/T	0.499998	0.000931757	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226883824	ATACGGAGCGAAGCA[C/T]GTGATCATGCTGTTT	5664
rs1295621	snp	A/T	0.388775	0.207946	intron-variant	PSEN2	GRCh38.p7	1:226873954	TTCCCACCCTCCCTT[A/T]TGCCCCAGAGAAGCA	5664
rs1295638	snp	A/G	0.493568	0.0563433	intron-variant	PSEN2	GRCh38.p7	1:226881566	GATCTTTGGTGCATA[A/G]TAGATGCACCACAGA	5664
rs1295640	snp	C/T	0.493568	0.0563433	intron-variant	PSEN2	GRCh38.p7	1:226882677	TGTGTGGACTGTTTT[C/T]TTGCAGCCAGTCTTA	5664
rs1295641	snp	C/T	0.493568	0.0563433	intron-variant	PSEN2	GRCh38.p7	1:226882994	TTTAGCTGTTCACCT[C/T]ATTAGCAAGGCAGCC	5664
rs1295642	snp	C/T	0.27893	0.24832	intron-variant	PSEN2	GRCh38.p7	1:226883347	TATCTCCTGGCCTGT[C/T]TCCTCCCATATCAGT	5664
rs1295643	snp	A/G	0.500006	0.00227077	intron-variant	PSEN2	GRCh38.p7	1:226883663	CATGGATAGGCTGCC[A/G]TGGGGGACATTCTGC	5664
rs1295644	snp	C/T	0.399449	0.200468	intron-variant	PSEN2	GRCh38.p7	1:226883676	CCGTGGGGGACATTC[C/T]GCGGCCCTCACGATG	5664
rs1295645	snp	C/T	0.256061	0.249927	utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871336	ACAGAAGCTAGTCCC[C/T]CCTCTGAATTTTACT	5664
rs1295646	snp	C/G	0.390464	0.206809	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226872038	TGTTGAAGTGCCCAT[C/G]TGCCAAGTCTTGAGT	5664
rs1295647	snp	C/T	0.493658	0.0559517	intron-variant	PSEN2	GRCh38.p7	1:226872975	CTGAGGTCGGAAGTT[C/T]GAGACCAGCCTGACC	5664
rs1295648	snp	C/T	0.257176	0.249897	intron-variant	PSEN2	GRCh38.p7	1:226873604	TATTTTTATTAGAGG[C/T]GGGGTTTCACCATGT	5664
rs1296171	snp	C/G	0.493154	0.0581045	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871905	AGAGCTGCGTCCTCA[C/G]GACGCCCACGTTGAG	5664
rs1297990	snp	C/T	0.38821	0.208322	intron-variant	PSEN2	GRCh38.p7	1:226872641	AGTGTGTGTAGGTCA[C/T]ATGCAGTGTGTCTAA	5664
rs1782530	snp	A/G	0.388964	0.20782	intron-variant	PSEN2	GRCh38.p7	1:226885130	CAGTTGCTTCAGCGG[A/G]TGGGGGTCGGGTAGT	5664
rs1794038	snp	G/T	0.492775	0.059668	intron-variant	PSEN2	GRCh38.p7	1:226886011	GCTAGGACTACAGGT[G/T]TGCACCACCATACCT	5664
rs1800675	snp	A/G	0.0154538	0.0865337	intron-variant	PSEN2	GRCh38.p7	1:226892641	GAAAGATCACTCTGC[A/G]GTGGGTCTGGAAGGA	5664
rs1800678	snp	C/T	0.471863	0.115225	intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226890891	CCCGTAGAGGAGAAT[C/T]GCCTGCAGCGTGGCC	5664
rs1800679	snp	C/T	0.0166325	0.0896639	intron-variant	PSEN2	GRCh38.p7	1:226888238	GCATGAGGACCTGGG[C/T]GGGGAAAGATGACCA	5664
rs1800680	snp	A/G	0.118933	0.212888	intron-variant	PSEN2	GRCh38.p7	1:226888283	TCCCCAGTGCCAGCC[A/G]TTTTGGGAACCCAGG	5664
rs1800681	snp	C/G	0.283421	0.247756	intron-variant	PSEN2	GRCh38.p7	1:226888522	TCTGTTCTATCGCCC[C/G]TTGATTTGGGATATC	5664
rs2073488	snp	A/G	0.388775	0.207946	intron-variant	PSEN2	GRCh38.p7	1:226875130	TGGGGCCTGTGGTCC[A/G]GGAGGGTGGTAGGGC	5664
rs2073489	snp	C/T	0.457504	0.139435	intron-variant	PSEN2	GRCh38.p7	1:226875970	AGAACGTAGTCTATG[C/T]TGGACACTTCCTTCT	5664
rs2105822	snp	C/T	0.446118	0.155041	intron-variant	PSEN2	GRCh38.p7	1:226893226	CTGAGCCACAGCACC[C/T]GGCCAAAATTAGTTT	5664
rs2236910	snp	C/G	0.364389	0.222519	intron-variant	PSEN2	GRCh38.p7	1:226885709	CTGCCCTCCAGCCAC[C/G]CTTCTCTCCGTCTGC	5664
rs2236912	snp	A/T	0.411242	0.191052	intron-variant	PSEN2	GRCh38.p7	1:226886040	CTGGCTAATTAAAAA[A/T]TTTTTTTTTGTGCAG	5664
rs2236913	snp	A/G	0.472147	0.114677	intron-variant	PSEN2	GRCh38.p7	1:226886424	CTGCCTATAGCTGCC[A/G]AGTAGCCCCAGGGAG	5664
rs2236914	snp	A/T	0.493201	0.0579089	intron-variant	PSEN2	GRCh38.p7	1:226891020	GATTCACCCGTGAAC[A/T]GTGAGGTCTTGGCTC	5664
rs2236915	snp	C/G	0.493247	0.0577133	intron-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226891521	TGCGGCTTGAAGATT[C/G]AGCAAGTGTTGGACC	5664
rs2246221	snp	A/G	0.496968	0.0388195	intron-variant	PSEN2	GRCh38.p7	1:226887701	TATGTTTGTCTATAT[A/G]TCATCTAACACCCCT	5664
rs2793461	snp	A/C	0.493568	0.0563433	intron-variant	PSEN2	GRCh38.p7	1:226874428	CGTTGATGGCCTTTA[A/C]GGTCCTTGCCAGCTC	5664
rs2793462	snp	C/T	0.388587	0.208071	intron-variant	PSEN2	GRCh38.p7	1:226875699	ATGTTAAGGCCAAAG[C/T]CTTTACATTTCTCTG	5664
rs2802267	snp	C/T	0.360933	0.225784	intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226891254	TAGCACCGCCTGAGA[C/T]GTGAACCTTTTCTCC	5664
rs2855559	snp	A/G	0.493293	0.0575177	intron-variant	PSEN2	GRCh38.p7	1:226892758	GATCCCACGGGGCCC[A/G]CAGGACTGGCCTCCC	5664
rs2855560	snp	A/C	0.493293	0.0575177	intron-variant	PSEN2	GRCh38.p7	1:226893327	CCTGGTGGGGGAAGG[A/C]GGACAGCTGGGGCCA	5664
rs2855561	snp	C/T	0.0569829	0.158885	intron-variant	PSEN2	GRCh38.p7	1:226893491	ACTAAAGAAAACAAA[C/T]GAGAGCATTTTGGAA	5664
rs2855562	snp	A/G	0.488529	0.0748607	intron-variant	PSEN2	GRCh38.p7	1:226894149	CTGGGGATGCGTCCA[A/G]CTGCCTCGTGGTGGG	5664
rs2855563	snp	A/G	0.254944	0.249951	intron-variant	PSEN2	GRCh38.p7	1:226894645	TAGTCAGTTAACGTG[A/G]CCAGATACACATAAT	5664
rs3213436	snp	A/G	0.284733	0.247575	intron-variant	PSEN2	GRCh38.p7	1:226893604	CTCTGTCTTGGTGTT[A/G]TATGGGCTTTTGAAT	5664
rs3213437	snp	G/T	0.0566069	0.158427	intron-variant	PSEN2	GRCh38.p7	1:226894366	GGTGAGGAGTGTACC[G/T]GCCCCAGCGTGGCTG	5664
rs3820649	snp	A/G	0.284209	0.247648	intron-variant	PSEN2	GRCh38.p7	1:226892751	TAGCACAGATCCCAC[A/G]GGGCCCGCAGGACTG	5664
rs3829979	snp	C/G	0.287085	0.247234	intron-variant	PSEN2	GRCh38.p7	1:226894404	AGCCTCCAGGCCGAG[C/G]ACCCAGCTGACAGCT	5664
rs3831497	in-del	-/AAG	0.492823	0.0594727	intron-variant	PSEN2	GRCh38.p7	1:226885968	CAACCTCCTGGGCTC[-/AAG]AAGTTCTCCCACCCA	5664
rs4653469	snp	A/G	0.0652144	0.168387	intron-variant	PSEN2	GRCh38.p7	1:226873721	GCGCTGGGCTGAGAT[A/G]ACCACTCTTAACATG	5664
rs4653470	snp	A/T	0.495174	0.0488838	intron-variant	PSEN2	GRCh38.p7	1:226895025	CCTGGCGGCTCTGAT[A/T]CCCTTGGTGCCAGCT	5664
rs6426553	snp	G/T	0.0217336	0.101961	synonymous-codon, nc-transcript-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226891294	TGCCATGGTGTGGAC[G/T]GTTGGCATGGCGAAG	5664
rs6426554	snp	A/G	0.373799	0.217195	intron-variant	PSEN2	GRCh38.p7	1:226894744	AGCCGTGCGCTTGGC[A/G]TCTGCCCCTTAGTGA	5664
rs6660082	snp	C/G	0.0948562	0.196037	intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871112	AGACCTCCGTTGCGC[C/G]GAGTCCATTCGGCCT	5664
rs6661000	snp	A/G	0.077417	0.180873	intron-variant	PSEN2	GRCh38.p7	1:226874349	catgggacattaact[A/G]attacttttgcccct	5664
rs6665033	snp	A/G	0.0329836	0.124112	utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871273	TCAGGCATTTCCAGC[A/G]GTGAGGAGACAGCCA	5664
rs6671059	snp	C/G	0.197703	0.244469	intron-variant	PSEN2	GRCh38.p7	1:226874784	GGAAATGAGCTGTGT[C/G]AGATTAGACTGTCTG	5664
rs6673248	snp	A/C			intron-variant	PSEN2	GRCh38.p7	1:226880599	CCTCTGGACAGCGAT[A/C]ACTCAGCCTCTGGAC	5664
rs6675452	snp	A/G	0.197703	0.244469	intron-variant	PSEN2	GRCh38.p7	1:226874456	CTCTGACATTGTCCT[A/G]TGGATATGTCCTTTC	5664
rs6677801	snp	A/G	0.117188	0.211804	intron-variant	PSEN2	GRCh38.p7	1:226880213	gaccctcatttctac[A/G]aaatattttaaaaat	5664
rs6677908	snp	A/G	0.197703	0.244469	intron-variant	PSEN2	GRCh38.p7	1:226880348	CACCACTGTACTCCA[A/G]CGTAAGTGACCAGTG	5664
rs6678839	snp	C/T	0.197703	0.244469	intron-variant	PSEN2	GRCh38.p7	1:226874627	AGGCTACCGTGTCCT[C/T]TCTCACTGTGTCCCT	5664
rs6678940	snp	C/T	0.197703	0.244469	intron-variant	PSEN2	GRCh38.p7	1:226874688	TTATTGAACATCTAC[C/T]GTGTGCTGGACACTT	5664
rs6680042	snp	G/T	0.113685	0.209567	intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226890677	tgctaggcattgggg[G/T]acccagcaggaaaga	5664
rs7512986	snp	C/G	0.0901694	0.192235	intron-variant	PSEN2	GRCh38.p7	1:226894992	CAGCCCCCACACCTG[C/G]TTCCCAGGGGCAGGT	5664
rs7519422	snp	A/G	0.0260105	0.111035	intron-variant	PSEN2	GRCh38.p7	1:226875308	AAGGTGAGCAGGGAA[A/G]CTGTGGGCAATTGTC	5664
rs7522645	snp	C/G	0.197703	0.244469	intron-variant	PSEN2	GRCh38.p7	1:226873888	AAGCAGATTTGATGG[C/G]TGTGTAGAGCATTTG	5664
rs7523790	snp	A/C	0.197703	0.244469	intron-variant	PSEN2	GRCh38.p7	1:226872789	GCCACAGCTGCGGAA[A/C]GGCGGGGGTGAGGCT	5664
rs7525819	snp	G/T	0.197703	0.244469	intron-variant	PSEN2	GRCh38.p7	1:226877272	TTGGAGATCTGCATT[G/T]TTAATAAGCAGCCTA	5664
rs7530286	snp	G/T			intron-variant	PSEN2	GRCh38.p7	1:226889214	GTAAAACAGAGGGGG[G/T]TCCACTATTTCTGGA	5664
rs7537037	snp	C/G	0.113685	0.209567	intron-variant, downstream-variant-500B	PSEN2	GRCh38.p7	1:226891600	GGTGGAGTGGGGGAA[C/G]CCCTGGTGTCAGGTG	5664
rs7539017	snp	C/G/T	0.000189617	0.00973532	synonymous-codon, nc-transcript-variant	PSEN2	GRCh38.p7	1:226889033	GTGGGTCATCCTGGG[C/G/T]GCCATCTCTGTGTAT	5664
rs7539119	snp	A/C	0.0905309	0.192535	intron-variant	PSEN2	GRCh38.p7	1:226889115	AAATCGTCCCCAGTG[A/C]TGCACAAGGAGGGCA	5664
rs7539129	snp	C/T			intron-variant	PSEN2	GRCh38.p7	1:226889143	GCAGGTGCTGAAGGG[C/T]TTGCATCCCTTTCTG	5664
rs7539221	snp	C/T	0.120367	0.215039	intron-variant	PSEN2	GRCh38.p7	1:226889254	GTGGTCTAGATAAAA[C/T]GCAGTAGTCACTGAG	5664
rs7543640	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226889257	GTCTAGATAAAACGC[A/G]GTAGTCACTGAGCTC	5664
rs7546338	snp	C/T	0	0	intron-variant	PSEN2	GRCh38.p7	1:226889197	CTGAGAGAGTCGCCT[C/T]TGTAAAACAGAGGGG	5664
rs7555739	snp	A/C	0.078151	0.181571	intron-variant	PSEN2	GRCh38.p7	1:226894882	ACCAGACTGCCTTAC[A/C]TGAGCCCTGCTGGCC	5664
rs10693643	in-del	-/TT	0.113685	0.209567	intron-variant	PSEN2	GRCh38.p7	1:226893099	ACCACACCTGGCTCA[-/TT]TTTATATTTTTAGTA	5664
rs10753428	snp	A/G	0.419936	0.183362	intron-variant	PSEN2	GRCh38.p7	1:226893921	GGGCTGGGCAAGAGC[A/G]GCTGGGCCTTCTGGG	5664
rs11578657	snp	A/T			intron-variant	PSEN2	GRCh38.p7	1:226892918	gcactacacttaaaa[A/T]tgcagtttgtttttt	5664
rs11582894	snp	A/C	0.5	0	intron-variant, nc-transcript-variant	PSEN2	GRCh38.p7	1:226890845	AACAGCTACAGAGTT[A/C]TAGGTACCTTCATGC	5664
rs11588886	snp	A/G	0.266	0.249487	intron-variant	PSEN2	GRCh38.p7	1:226873784	TTATCTATTAAAACA[A/G]TAGAGGGAGGGAACC	5664
rs11799808	snp	G/T			intron-variant	PSEN2	GRCh38.p7	1:226886676	GTAGATAGAAGTGCA[G/T]AGTGCCCAGGCTAGA	5664
rs11804915	snp	C/T	0.0577344	0.159793	intron-variant	PSEN2	GRCh38.p7	1:226890366	TCCCTGACTTCATCC[C/T]GTCCATCCTCCAGCG	5664
rs12027512	snp	A/C	0	0	intron-variant	PSEN2	GRCh38.p7	1:226873500	agctaactgcaacct[A/C]tgcttgccgggttct	5664
rs12057618	snp	A/C	0.117188	0.211804	intron-variant	PSEN2	GRCh38.p7	1:226884002	CAGCCTGTGTTGGTC[A/C]CTGTACCTGCAGCTC	5664
rs12058836	snp	G/T	0.00438332	0.0466095	intron-variant	PSEN2	GRCh38.p7	1:226886539	AGGCTTTTCTCCCAG[G/T]TAAGGGGTTGAACCC	5664
rs12069540	snp	C/T	0.157972	0.232445	intron-variant	PSEN2	GRCh38.p7	1:226886301	AGGCTCCCCTCACCC[C/T]GATACTTCCCCTGAA	5664
rs12070751	snp	A/G	0.132066	0.220435	intron-variant	PSEN2	GRCh38.p7	1:226894737	GCGTCTGAGCCGTGC[A/G]CTTGGCATCTGCCCC	5664
rs12071324	snp	C/G	0.117188	0.211804	intron-variant	PSEN2	GRCh38.p7	1:226882173	ATGATGAGGATTGGC[C/G]GAAAAGGTGGGTGGC	5664
rs12091957	snp	A/C	0.174932	0.238463	intron-variant	PSEN2	GRCh38.p7	1:226874011	ATGTGGGCACTCCCC[A/C]CCATGGAGCCAAACC	5664
rs12093600	snp	A/G	0.0295035	0.117819	intron-variant, upstream-variant-2KB	PSEN2, LOC105373119	GRCh38.p7	1:226871702	AAGGAAGCCTCTGAT[A/G]CCTCTGTAGCCAATT	5664
rs12096062	snp	A/G			intron-variant	PSEN2	GRCh38.p7	1:226878640	GCCTGTGGCTTTTTA[A/G]GTACAGGGACTCCCA	5664
rs12097722	snp	A/G	0.136506	0.222754	intron-variant	PSEN2	GRCh38.p7	1:226874246	AACCCTGGCCACTGG[A/G]TACGTGACCCTCACA	5664
rs12123818	snp	A/G	0.284209	0.247648	intron-variant	PSEN2	GRCh38.p7	1:226892120	GGCTAAGGAGACACG[A/G]GCAGTAATCACATAG	5664
rs12130732	snp	C/T	0.264906	0.249555	intron-variant	PSEN2	GRCh38.p7	1:226891999	AGAAGATGCCTGCAG[C/T]GCTGGGGTCTTCTCA	5664
rs12401969	snp	C/T	0.39121	0.2063	intron-variant	PSEN2	GRCh38.p7	1:226884566	TTTTAAAGTTAGGGA[C/T]TTTTGTTTCATTTCG	5664

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