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
rs178918	snp	C/T	0.0854556	0.188216	upstream-variant-2KB, intron-variant	PARP3, RRP9	GRCh38.p7	3:51940650	gtgtgcacctgtagt[C/T]ccaactactcaggag	9136
rs191237	snp	G/T	0	0	intron-variant	RRP9	GRCh38.p7	3:51936383	AGGTCTGGTGCATGG[G/T]GGGTGCCTGTGATCA	9136
rs323865	snp	G/T	0.141596	0.225274	upstream-variant-2KB, intron-variant	PARP3, RRP9	GRCh38.p7	3:51941305	GAATCCAAGACTCTG[G/T]CCCTTGGCTCTGAGA	9136
rs323866	snp	C/G	0.141934	0.225437	upstream-variant-2KB, intron-variant	PARP3, RRP9	GRCh38.p7	3:51941702	GGCTGGGGAAGGGCC[C/G]GGACCCAGGTCCCCT	9136
rs323867	snp	A/G	0.142272	0.225598	intron-variant, upstream-variant-2KB	PARP3, RRP9	GRCh38.p7	3:51943165	CCCCAGACCACACCC[A/G]GCTCTTTGTCACTCA	9136
rs323886	snp	C/G/T	0.226006	0.249916	downstream-variant-500B	RRP9	GRCh38.p7	3:51933423	TCTTTTGGGCCTTGT[C/G/T]TCTTGTAGCTTCTTG	9136
rs323887	snp	A/G	0.202651	0.245475	intron-variant	RRP9	GRCh38.p7	3:51934413	GCCTAGGCCCCTGGA[A/G]TTAGCTCTTTAAGGT	9136
rs323888	snp	A/G	0.00413385	0.0452751	intron-variant	RRP9	GRCh38.p7	3:51935509	TCATGCAGTACCCCT[A/G]TCCCCACTATCCTGC	9136
rs323889	snp	A/G	0.0700422	0.173537	intron-variant	RRP9	GRCh38.p7	3:51936150	GAACCTGCATCCTGG[A/G]GTAGCGAGTGGGTAG	9136
rs323898	snp	A/G	0.0909642	0.192893	intron-variant	RRP9	GRCh38.p7	3:51937366	GGGGTTGGTGAAGGT[A/G]GTGCCTTTATGCCAC	9136
rs323899	snp	A/G	0.0040768	0.0449642	intron-variant	RRP9	GRCh38.p7	3:51937756	GCCTCAGTTTACTTG[A/G]TCTGGTCTGTCCTGC	9136
rs323900	snp	G/T	0.0290216	0.116912	intron-variant	RRP9	GRCh38.p7	3:51938239	GTCAGAGGAACAAGG[G/T]GAGCCCCTCAGACCC	9136
rs323901	snp	C/T	0.0126979	0.078662	intron-variant	RRP9	GRCh38.p7	3:51939153	GAGTCTTGGGAAACA[C/T]GGTTAGGGGAGTGGA	9136
rs368210	snp	G/T	0.0850919	0.187897	upstream-variant-2KB	PARP3, RRP9	GRCh38.p7	3:51942278	GCCGGGCTGCCCATG[G/T]AGGGGAGGAGTCACG	9136
rs380922	snp	A/T	0.0850919	0.187897	upstream-variant-2KB	PARP3, RRP9	GRCh38.p7	3:51942277	CCGGGCTGCCCATGG[A/T]GGGGAGGAGTCACGT	9136
rs929533	snp	A/G	0.451234	0.14834	upstream-variant-2KB, intron-variant	PARP3, RRP9	GRCh38.p7	3:51941561	CTGAGGGAACCGAGG[A/G]GGGGGGGCCCTTGGT	9136
rs4687604	snp	A/G/T	5.37909e-05	0.0051858	upstream-variant-2KB, missense	PARP3, RRP9	GRCh38.p7	3:51941830	CCGGCCCCAGAGGCC[A/G/T]GCTTTCCCCGCTTAC	9136
rs4687791	snp	C/G	0.00159617	0.0282053	intron-variant	RRP9	GRCh38.p7	3:51936691	CCTGGCTCAGCCACC[C/G]TGAGCCTCCGGACAA	9136
rs5848937	in-del	-/C			upstream-variant-2KB, intron-variant	PARP3, RRP9	GRCh38.p7	3:51941563	AAGGGCCCCCCCCCC[-/C]TCGGTTCCCTCAGAA	9136
rs7627182	snp	C/T	0.0298908	0.118541	intron-variant, upstream-variant-2KB	PARP3, RRP9	GRCh38.p7	3:51942921	TCCTCTGCCCACCCT[C/T]CCCCATAGCTCGGTG	9136
rs11709032	snp	C/G	0.000399281	0.0141238	intron-variant	RRP9	GRCh38.p7	3:51935096	AAAGAGGTTACAACA[C/G]CTCCCCCACTGGGGG	9136
rs12494290	snp	C/T			intron-variant	RRP9	GRCh38.p7	3:51938550	gcatctcaacagcaa[C/T]actgagaacaagaag	9136
rs34377869	in-del	-/AAG			cds-indel, upstream-variant-2KB	PARP3, RRP9	GRCh38.p7	3:51943407	GGCCCTGAGAAGAAG[-/AAG]GGCCGGCAGGCAGGA	9136
rs34462499	in-del	-/G			frameshift-variant	RRP9	GRCh38.p7	3:51934478	TCACTCACCAGGGGG[-/G]ATGTCACAGAGAAGG	9136
rs34462541	in-del	-/G			intron-variant	RRP9	GRCh38.p7	3:51934564	GCCTGGGGAGACTGG[-/G]AACAGTGAGCAACCC	9136
rs34691234	snp	C/T	0	0	intron-variant	RRP9	GRCh38.p7	3:51933856	CATCACAGTCAAGGG[C/T]TGGGCCTTATCAGGC	9136
rs34860798	in-del	-/G			intron-variant	RRP9	GRCh38.p7	3:51935111	CTCCCCCACTGGGGG[-/G]TGCCCTGAGGCAAGC	9136
rs35147971	in-del	-/G			intron-variant	RRP9	GRCh38.p7	3:51935272	CCCCTGGAGAAAGGG[-/G]CTGTGAGGAGCGTGG	9136
rs41291740	snp	A/G	0.0138799	0.0821421	intron-variant	RRP9	GRCh38.p7	3:51933999	TAGCAGTGAGTTTGT[A/G]AGGATGAAGGAGGCA	9136
rs41291742	snp	A/G/T	0.0158294	0.0875461	missense, synonymous-codon	RRP9	GRCh38.p7	3:51935202	GACCTCTTACCCATC[A/G/T]TCCGCGCCGGACACC	9136
rs41292344	snp	A/G	0.00517822	0.0506191	intron-variant	RRP9	GRCh38.p7	3:51935915	TGCTCAGGCTGGAGT[A/G]CAGTGGTGCGATCAT	9136
rs41292346	snp	A/G	1.64795e-05	0.00287045	missense	RRP9	GRCh38.p7	3:51937291	GCCCCCGTAAAACGC[A/G]AATGTCAGCTGAGGC	9136
rs45494795	snp	C/T	0.000399281	0.0141238	intron-variant	RRP9	GRCh38.p7	3:51936802	AAAAGGGCTTTGGGA[C/T]TGATGGTGTGAGTTC	9136
rs55777183	in-del	-/T			intron-variant	RRP9	GRCh38.p7	3:51935769	GGCCCAGGGAGGACT[-/T]CCCAAAAAGCAAGCC	9136
rs55980237	snp	A/C			downstream-variant-500B	RRP9	GRCh38.p7	3:51933018	AGGGTCCCACTCCCA[A/C]TCCTGACCCCCACAC	9136
rs56746340	snp	C/T	0.0592355	0.161582	upstream-variant-2KB, intron-variant	PARP3, RRP9	GRCh38.p7	3:51940471	AAATGAGGGAGGCAT[C/T]CAAAGCCCTCTACAA	9136
rs61729070	snp	C/G/T	0.00660737	0.057168	missense, upstream-variant-2KB	PARP3, RRP9	GRCh38.p7	3:51943369	CCATGGCTCCAAAGC[C/G/T]GAAGCCCTGGGTACA	9136
rs61729073	snp	A/G	0.000197945	0.00994651	synonymous-codon	RRP9	GRCh38.p7	3:51935603	TCACAGCGTCTCCAC[A/G]TAGGAGTTCTCTGCC	9136
rs62259752	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	PARP3, RRP9	GRCh38.p7	3:51942369	CCCAAGGTCACCGCG[C/T]GACCGGCAGATGCGT	9136
rs71297380	snp	C/T	0.5	0	upstream-variant-2KB, intron-variant	PARP3, RRP9	GRCh38.p7	3:51941239	TTCCCACCCAGAGAC[C/T]TCGCAGAAACAAGAC	9136
rs72961999	snp	A/G	0.0592355	0.161582	intron-variant, upstream-variant-2KB	PARP3, RRP9	GRCh38.p7	3:51943900	CCATACCTCCATGTC[A/G]GGGTTTAGCCATGTC	9136
rs73838923	snp	G/T	0.00868199	0.0653117	intron-variant	RRP9	GRCh38.p7	3:51935512	GGATAGTGGGGATAG[G/T]GGTACTGCATGAACT	9136
rs74869207	snp	C/G	0.0383715	0.133092	downstream-variant-500B	RRP9	GRCh38.p7	3:51933034	TCCTGACCCCCACAC[C/G]TCACGGCAGTCTGTC	9136
rs74879881	snp	C/T	0.00123515	0.0248203	upstream-variant-2KB, intron-variant	PARP3, RRP9	GRCh38.p7	3:51941401	CTATGTGGAAAAGAA[C/T]AGCTCACCTCTCGCT	9136
rs75375232	snp	A/G	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	PARP3, RRP9	GRCh38.p7	3:51943192	GGGGCTGGGAATGCC[A/G]TCAGAGTGGACACAG	9136
rs75503977	snp	A/G	0.00358779	0.0422022	intron-variant	RRP9	GRCh38.p7	3:51937899	CTGCCTTTACTTATC[A/G]GATCAGCCCCCTGCG	9136
rs76091063	snp	C/T	0.00113634	0.0238092	synonymous-codon	RRP9	GRCh38.p7	3:51937277	GATAGAGAGCTGGTG[C/T]CCCCGTAAAACGCGA	9136
rs76244899	snp	A/G	0.00318978	0.0398085	intron-variant	RRP9	GRCh38.p7	3:51939591	TAGAGGTGGTCACAC[A/G]ACTGTGTGTGTTTGT	9136
rs76493375	snp	A/G	0.00318978	0.0398085	downstream-variant-500B	RRP9	GRCh38.p7	3:51933039	ACCCCCACACCTCAC[A/G]GCAGTCTGTCCCCTC	9136
rs76545705	snp	A/G	0.046775	0.145601	intron-variant, upstream-variant-2KB	PARP3, RRP9	GRCh38.p7	3:51942839	GAGTCCATTGGGAAG[A/G]GCTTCTACAGCTCTG	9136
rs77190690	snp	C/G	0.000169986	0.00921758	intron-variant, upstream-variant-2KB	PARP3, RRP9	GRCh38.p7	3:51942757	AGGGCAAGGCCTGGT[C/G]GGACTGGCCTTTGCC	9136
rs77684818	snp	A/G	0.5	0	upstream-variant-2KB, intron-variant	PARP3, RRP9	GRCh38.p7	3:51940339	CGAGTTCTAAAGTCA[A/G]CTCATAGGGAAGGCA	9136
rs77898224	snp	A/G/T	0.00884991	0.0659314	missense, upstream-variant-2KB	PARP3, RRP9	GRCh38.p7	3:51943476	CTCAAGGCCATACCC[A/G/T]CAGAGAAGCGCATAA	9136
rs77910908	snp	G/T	0	0	upstream-variant-2KB, intron-variant	PARP3, RRP9	GRCh38.p7	3:51940693	CTAACTTTTTTTTTT[G/T]GTACAGACAAGATCT	9136
rs77991114	snp	C/G	0.0137256	0.0816972	intron-variant	RRP9	GRCh38.p7	3:51934802	GGAGGGAATACAGCA[C/G]TGAGGGGGCCAGAGG	9136
rs78405934	snp	C/T	0.0150606	0.0854603	intron-variant	RRP9	GRCh38.p7	3:51935881	ATTTATTTTTTTTAG[C/T]GACAGGGTCTCATTC	9136
rs79127582	snp	C/T	0.00318978	0.0398085	upstream-variant-2KB, intron-variant	PARP3, RRP9	GRCh38.p7	3:51940818	AGGCCCAGCCCCCTT[C/T]CATCTTTTCTACTGC	9136
rs79152342	snp	C/T	0.00318978	0.0398085	intron-variant	RRP9	GRCh38.p7	3:51937374	AAGGCACTACCTTCA[C/T]CAACCCCACTGCGTA	9136
rs80278469	snp	G/T	0.079617	0.182947	intron-variant	RRP9	GRCh38.p7	3:51938666	GCCAGGTGTGCAAGG[G/T]GCCATGGAATTTTCT	9136
rs111654088	snp	A/C/G	0.000261847	0.0114395	upstream-variant-2KB, missense	PARP3, RRP9	GRCh38.p7	3:51941839	GAGGCCGGCTTTCCC[A/C/G]GCTTACGAGCAGCCG	9136
rs112354680	snp	A/G	0.5	0	intron-variant	RRP9	GRCh38.p7	3:51935085	CTCATCCATGAAAAG[A/G]GGTTACAACAGCTCC	9136
rs112368813	in-del	-/CT	0.0209421	0.100162	intron-variant	RRP9	GRCh38.p7	3:51940249	GGCAACAGAGTGAGA[-/CT]CTGTCTCAAAAACAA	9136
rs112476373	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB, utr-variant-5-prime	PARP3, RRP9	GRCh38.p7	3:51943021	GAGAGCCTCCTTTCA[C/T]TTTCCCTACCCCTCA	9136
rs112817696	snp	C/T	0.0168179	0.0901449	synonymous-codon, upstream-variant-2KB	PARP3, RRP9	GRCh38.p7	3:51943496	GAAGCGCATAATCCG[C/T]GTGGATCCAACATGT	9136
rs112818638	snp	C/T	0.5	0	upstream-variant-2KB	PARP3, RRP9	GRCh38.p7	3:51941958	GCAAGACCCCGCGTA[C/T]TGATAGGCTTCCACC	9136
rs113421043	snp	C/T	0.00835141	0.0640778	intron-variant	RRP9	GRCh38.p7	3:51938988	CCATGCCCCAGCCCC[C/T]GGACCAGCTGAGAGT	9136
rs113431018	snp	A/G	0.0271762	0.113356	intron-variant	RRP9	GRCh38.p7	3:51940055	TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA	9136
rs113720405	snp	A/G	0.5	0	intron-variant	RRP9	GRCh38.p7	3:51935989	TCTCGGCCTCCCAAA[A/G]TGCTAGGATTATAGG	9136
rs113804016	snp	C/T	6.59174e-05	0.00574059	missense	RRP9	GRCh38.p7	3:51937290	TGCCCCCGTAAAACG[C/T]GAATGTCAGCTGAGG	9136
rs114015035	snp	A/G	0.0185938	0.0946107	intron-variant, upstream-variant-2KB	PARP3, RRP9	GRCh38.p7	3:51943761	AGGCCTCCTCCCACC[A/G]CACTTAGGGAAAGGC	9136
rs114055246	snp	A/G	0.00123513	0.0248201	intron-variant	RRP9	GRCh38.p7	3:51936402	TGCACCAGACCTCCC[A/G]CCTGCCCCCAGGGCC	9136
rs114270966	snp	C/T	0.0379877	0.132479	upstream-variant-2KB, intron-variant	PARP3, RRP9	GRCh38.p7	3:51940709	GTACAGACAAGATCT[C/T]GCTATGTTGCCCAGG	9136
rs114757525	snp	A/C/G	0.0456997	0.144133	intron-variant	RRP9	GRCh38.p7	3:51933817	GAAAGACATTAGAAC[A/C/G]CCCCCCGCCACCACC	9136
rs115048568	snp	C/T	0.0185938	0.0946107	intron-variant, upstream-variant-2KB	PARP3, RRP9	GRCh38.p7	3:51943676	CAAGGCCATGTTCTC[C/T]TGACCCCAGACATCA	9136
rs115210290	snp	A/G	0.0376037	0.131863	intron-variant	RRP9	GRCh38.p7	3:51939953	CCCACAATAACCTTC[A/G]GATTAAGAAAAGTAC	9136
rs115426717	snp	G/T	0.0147357	0.084562	missense	RRP9	GRCh38.p7	3:51936280	CATCCCGGTGTCCTG[G/T]GAAGGTGTACAAGTG	9136
rs115655439	snp	A/G/T	0.0807149	0.183963	intron-variant	RRP9	GRCh38.p7	3:51936849	GGTGTAGAAGGAACC[A/G/T]CTGGTCAGCCAGCAA	9136
rs115711615	snp	A/G	0.00318978	0.0398085	intron-variant	RRP9	GRCh38.p7	3:51938708	TTTAGGAAGGATAGA[A/G]GCTGTGCTCCCAAAC	9136
rs115746833	snp	C/T	0.00124223	0.0248912	synonymous-codon	RRP9	GRCh38.p7	3:51935449	GCTCAAGGCATCCAG[C/T]GCAGCCACAGCGTCC	9136
rs115906487	snp	C/G	0.00676609	0.0577691	intron-variant	RRP9	GRCh38.p7	3:51936929	CTCAAATGTCTTCTA[C/G]TCCAACCACCTACCT	9136
rs115983390	snp	C/T	0.00318978	0.0398085	intron-variant	RRP9	GRCh38.p7	3:51938325	TGCTAGCCCACATGG[C/T]CGGTGACTACACTGC	9136
rs116065853	snp	C/T	0.00517822	0.0506191	intron-variant	RRP9	GRCh38.p7	3:51937883	GCTGGAGGGTTTCCT[C/T]CTGCCTTTACTTATC	9136
rs116158470	snp	A/G	0.0260105	0.111035	intron-variant, upstream-variant-2KB	PARP3, RRP9	GRCh38.p7	3:51943801	ATCAGTCTCCTGGGC[A/G]CTTGCCCATGTCCCC	9136
rs116174224	snp	A/G	0.00233187	0.034066	synonymous-codon	RRP9	GRCh38.p7	3:51935473	AGCGTCCTGGTGTCC[A/G]AAGCTAGAGGGCCGG	9136
rs116265482	snp	A/G/T	0.00198807	0.0314766	intron-variant	RRP9	GRCh38.p7	3:51937162	CGGATCCGCCATGGG[A/G/T]GCTCCAGCCCCACCC	9136
rs116395477	snp	A/G	0.00318978	0.0398085	downstream-variant-500B	RRP9	GRCh38.p7	3:51933235	TAGCCTGAGGAGGTC[A/G]TGCAGGACACGCAGG	9136
rs116614473	snp	C/T	0.00122593	0.0247277	intron-variant	RRP9	GRCh38.p7	3:51935555	CTCCCACACCCTCTC[C/T]CACACCATCCACACA	9136
rs116788287	snp	C/T	0.078151	0.181571	intron-variant	RRP9	GRCh38.p7	3:51938819	TATCCCCAGACATGA[C/T]GGGGGCAGTCTGGAT	9136
rs137940457	snp	C/T	0.00159617	0.0282053	intron-variant	RRP9	GRCh38.p7	3:51934830	AGGCAGAAAAGGCCC[C/T]CTGTGTAACACAAAG	9136
rs138014839	snp	C/T	0.000153988	0.00877328	missense	RRP9	GRCh38.p7	3:51935210	ACCCATCGTCCGCGC[C/T]GGACACCATGTGCTC	9136
rs138270147	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	PARP3, RRP9	GRCh38.p7	3:51942076	AGCCCCGCCTCCTGA[A/G]GTTCCTAGGCTCCCG	9136
rs138321463	snp	A/G	0.000798403	0.0199641	intron-variant	RRP9	GRCh38.p7	3:51935093	TGAAAAGAGGTTACA[A/G]CAGCTCCCCCACTGG	9136
rs138379396	snp	C/T	0.000399281	0.0141238	intron-variant	RRP9	GRCh38.p7	3:51938380	CAAACTAAAAGGCCC[C/T]ACTCAGTGCCCCACG	9136
rs138383214	snp	C/T	9.89887e-05	0.00703452	synonymous-codon	RRP9	GRCh38.p7	3:51937690	CTCCTTCAGGCGCCC[C/T]GCCACCTGGTCCTCC	9136
rs138782179	snp	A/G	6.64198e-05	0.00576242	missense	RRP9	GRCh38.p7	3:51935406	GTACAGTCCCATCCC[A/G]GCCCCCAGCCGTCAC	9136
rs138809721	snp	A/G	0.00676609	0.0577691	utr-variant-5-prime, upstream-variant-2KB	PARP3, RRP9	GRCh38.p7	3:51942565	CACAAGCTCATCCCC[A/G]GCCTCTGGCGATTGT	9136
rs139078231	in-del	-/G	0.00318978	0.0398085	intron-variant	RRP9	GRCh38.p7	3:51937395	CCACTGCGTAGTGTT[-/G]GCCTTTCCCACCCAG	9136
rs139292236	in-del	-/AGA	0.00623366	0.0554795	cds-indel, upstream-variant-2KB	PARP3, RRP9	GRCh38.p7	3:51943399	AGACTGAGGGCCCTG[-/AGA]AGAAGAAGGGCCGGC	9136
rs139357193	snp	A/C	0.0142736	0.0832652	intron-variant	RRP9	GRCh38.p7	3:51937982	CACTGACAGCCTGGG[A/C]ACCCACTGGGAATCC	9136
rs139457127	snp	C/T	0.000798403	0.0199641	intron-variant	RRP9	GRCh38.p7	3:51939829	TTTACCATTACTCTC[C/T]GTAGTGCAAATATAT	9136

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