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
rs9626	snp	C/T	0.419305	0.183945	synonymous-codon	NACC2	GRCh38.p7	9:136011825	CCCCGAGTTCCCGCC[C/T]GCCGCGGCACAGGTG	138151
rs9753	snp	C/T	0.31352	0.241796	synonymous-codon	NACC2	GRCh38.p7	9:136011789	GCAACGCATCTACGC[C/T]GAGCGGCGGGGCGAC	138151
rs871093	snp	A/G	0.0209421	0.100162	intron-variant	NACC2	GRCh38.p7	9:136063057	TCACTGTTTTCTTCT[A/G]ATTTTTGTTCTCGTT	138151
rs871094	snp	C/T	0.156319	0.231784	intron-variant	NACC2	GRCh38.p7	9:136062849	CTAAGCCTGGGAGGC[C/T]GAGGCCGCAGTGTGC	138151
rs871095	snp	A/G	0.432944	0.170387	intron-variant	NACC2	GRCh38.p7	9:136063400	GCTTCTGCAATGTAC[A/G]TGACCTCTTTCCTGG	138151
rs884558	snp	A/G	0	0	intron-variant	NACC2	GRCh38.p7	9:136047756	GCTGCGGTCCTGCTG[A/G]CTCCCCAAAAACCCA	138151
rs884559	snp	C/T	0	0	intron-variant	NACC2	GRCh38.p7	9:136047816	CTCACGAAGTCCAGG[C/T]GATGTGAGGGCTTAA	138151
rs939612	snp	C/T	0	0	intron-variant	NACC2	GRCh38.p7	9:136048701	CCTGTGCAGCGTCTG[C/T]CACCACAGCCGGGAC	138151
rs939613	snp	G/T	0	0	intron-variant	NACC2	GRCh38.p7	9:136048451	GGTAGGGCTTGATTT[G/T]TCCTGAGACTGGGAG	138151
rs1007411	snp	C/T	0.040671	0.13668	intron-variant	NACC2	GRCh38.p7	9:136043730	CAGGGTAACATTCTA[C/T]AGGAGGGAACTGTTC	138151
rs1107549	snp	C/T	0	0	intron-variant	NACC2	GRCh38.p7	9:136049174	CTCGGCTCAGCACAC[C/T]GGGCGCTTCCTGGCC	138151
rs1164962	snp	C/T	0.00517822	0.0506191	intron-variant	NACC2	GRCh38.p7	9:136024184	cacacacacacactc[C/T]gtcctcacacacaca	138151
rs1183712	snp	C/T	0.5	0	intron-variant	NACC2	GRCh38.p7	9:136024454	CTCTGTCCTCACACA[C/T]ACCCTCTGTCCTCAC	138151
rs1335098	snp	A/C	0.251014	0.249998	intron-variant	NACC2	GRCh38.p7	9:136035262	accacctggcagaga[A/C]cacctgcaccaaacc	138151
rs1335099	snp	C/T	0.0926964	0.194308	intron-variant	NACC2	GRCh38.p7	9:136035337	ACTCCTGTGACGCAC[C/T]GAGAAGGTTCCGCTG	138151
rs1402643	snp	A/G			intron-variant	NACC2	GRCh38.p7	9:136028184	TCTCTCTGTCACtca[A/G]gctggatgctcctgc	138151
rs1464424	snp	A/G	0.375	0.216506	intron-variant	NACC2	GRCh38.p7	9:136046947	TCCACCCTCTCTCGC[A/G]TTAAGAACCATGGAC	138151
rs1464425	snp	C/T	0.375	0.216506	intron-variant	NACC2	GRCh38.p7	9:136046760	CCTCCCTCCAGGTCC[C/T]GCGTCACCACCCGTC	138151
rs1521444	snp	C/G			intron-variant	NACC2	GRCh38.p7	9:136043727	CCCCAGGGTAACATT[C/G]TACAGGAGGGAACTG	138151
rs1572290	snp	A/G	0.417359	0.185718	intron-variant	NACC2	GRCh38.p7	9:136032006	GGGGTGCTGCCGAGG[A/G]CGACCCTTGCCCCCC	138151
rs1572291	snp	A/C	0.173965	0.238157	intron-variant	NACC2	GRCh38.p7	9:136032003	GTGCTGCCGAGGACG[A/C]CCCTTGCCCCCCATT	138151
rs1615391	snp	C/T	0.0715223	0.175059	intron-variant	NACC2	GRCh38.p7	9:136090916	CACTTTCAGGCCCCT[C/T]TGTTCCCCGCCCCCA	138151
rs1717416	snp	C/T	0.499154	0.0205497	intron-variant	NACC2	GRCh38.p7	9:136090835	TCCCAAGCCCAGGGC[C/T]GGCCGGCCCCAGCTC	138151
rs1717417	snp	A/G	0.0995161	0.199636	intron-variant	NACC2	GRCh38.p7	9:136090548	TGGGTGCCTGCTGAG[A/G]GAAGACTTGCTAGCA	138151
rs1717418	snp	A/C	0.489376	0.0721049	intron-variant	NACC2	GRCh38.p7	9:136090247	GGACCCCTGAGGCAT[A/C]CCCTCTGGCCAGGGC	138151
rs1717451	snp	A/G	0.304688	0.243945	intron-variant	NACC2	GRCh38.p7	9:136093846	CCTAGAGTTAGGTCA[A/G]GGTTCAGGCAGCCCC	138151
rs1717452	snp	C/T	0.305436	0.243776	intron-variant	NACC2	GRCh38.p7	9:136093715	AAAGAGGCCTCTTGG[C/T]GTTTTCCCCTGGGGT	138151
rs1717453	snp	A/G	0.304937	0.243889	intron-variant	NACC2	GRCh38.p7	9:136093588	TGGAATGGGCACAGA[A/G]AGTGGAACAAGATAT	138151
rs1717454	snp	G/T	0.305186	0.243833	intron-variant	NACC2	GRCh38.p7	9:136093381	GGCTGCTGGAAGGGT[G/T]CGCAGGGCTGCTCTG	138151
rs1717455	snp	C/T	0.305186	0.243833	intron-variant	NACC2	GRCh38.p7	9:136093295	TTTCCAATTAAAGCA[C/T]GAGGCTGCATTATTC	138151
rs1717456	snp	A/G	0.305186	0.243833	intron-variant	NACC2	GRCh38.p7	9:136093230	TTCTTCCAGGCCTGC[A/G]CTCCTCTTGGCCTCT	138151
rs1717457	snp	C/T	0.304937	0.243889	intron-variant	NACC2	GRCh38.p7	9:136093127	AAGGTGTTGTCCTTT[C/T]CGGGATGTTGAGTTC	138151
rs1996743	snp	C/G	0.5	0	intron-variant, upstream-variant-2KB	NACC2	GRCh38.p7	9:136052929	CCTGGGCTCATACCA[C/G]CCTCTCTGCGTGGGG	138151
rs2139881	snp	C/T	0.301681	0.2446	intron-variant	NACC2	GRCh38.p7	9:136021694	ATGCCCCAGGCTAGA[C/T]GCAGCCCGGATGTCC	138151
rs2139882	snp	A/G	0.284209	0.247648	intron-variant	NACC2	GRCh38.p7	9:136029992	ACAGAGGTTTCTGGC[A/G]GGTGAAGCGACACCC	138151
rs2275107	snp	A/G	0.248847	0.250004	synonymous-codon, downstream-variant-500B	NACC2, LOC105376322	GRCh38.p7	9:136016404	GCCTGAGCCAGTGCC[A/G]CTGGAGAGCCGCTCC	138151
rs2275108	snp	C/G	0.00279162	0.0372561	intron-variant, nc-transcript-variant	NACC2, LOC105376322	GRCh38.p7	9:136015933	AGTTGCAGCCTTTGA[C/G]GGTAACGGCCAGGTT	138151
rs2280484	snp	C/G	0.241053	0.24984	intron-variant, upstream-variant-2KB	NACC2, LOC105376322	GRCh38.p7	9:136012994	ATCACACTTGGAAAC[C/G]TACCAAGAACGTTAA	138151
rs2280485	snp	C/T	0.494624	0.051568	intron-variant, upstream-variant-2KB	NACC2, LOC105376322	GRCh38.p7	9:136013151	CCTCAGGCTGGGATC[C/T]GAACCCAGCCCCGGC	138151
rs2280486	snp	C/T	0.491337	0.0652412	synonymous-codon, upstream-variant-2KB	NACC2, LOC105376322	GRCh38.p7	9:136013290	GCAGCTGTTGGCCAG[C/T]GTGTTCCTGGTGGAG	138151
rs2280487	snp	C/G	0.40263	0.198	intron-variant, upstream-variant-2KB	NACC2, LOC105376322	GRCh38.p7	9:136013368	GGCGACCCGCCCGCA[C/G]GAATGCCCTGCTGGG	138151
rs2385188	snp	C/T	0.472522	0.113946	intron-variant	NACC2	GRCh38.p7	9:136063355	GAGGGGCTCGAGTCC[C/T]GTGCCTATTGGTCAT	138151
rs3004014	snp	C/T	0.0685596	0.171987	upstream-variant-2KB	NACC2	GRCh38.p7	9:136096229	TCGGGACCACTGAGG[C/T]GGTATCACTCCATTC	138151
rs3811129	snp	C/T	0.221737	0.248397	utr-variant-3-prime	NACC2	GRCh38.p7	9:136009832	CCCCTCCGGTGTGCA[C/T]ACAGGCCAGTGAGCG	138151
rs3811130	snp	A/G	0.331179	0.236453	utr-variant-3-prime	NACC2	GRCh38.p7	9:136009810	CAGTGAGCGGTGGCC[A/G]ACCAGCGCACCCCAC	138151
rs3811131	snp	G/T	0.331411	0.236373	utr-variant-3-prime	NACC2	GRCh38.p7	9:136009737	TAGGGGAGGACCATG[G/T]GCTGCACCCTGGCCT	138151
rs3841030	in-del	-/C	0.471768	0.115407	utr-variant-3-prime	NACC2	GRCh38.p7	9:136009844	GCCCATCAGCACCCC[-/C]TCCGGTGTGCACACA	138151
rs3922922	snp	A/G	0.360421	0.224293	intron-variant	NACC2	GRCh38.p7	9:136074866	TCGGCTGGGAAGGCC[A/G]CGCTTCCTGCCGCTC	138151
rs4384058	snp	C/T	0.0471551	0.14613	intron-variant	NACC2	GRCh38.p7	9:136075305	AGAGCTGGCTGCGGC[C/T]GCCTGGCTGGGATAC	138151
rs4409473	snp	C/T	0.462034	0.132445	intron-variant	NACC2	GRCh38.p7	9:136031934	CACAGCTGATGTGTA[C/T]GGGCAGCTGTTAACA	138151
rs4419885	snp	C/G	0.493477	0.0567349	intron-variant	NACC2	GRCh38.p7	9:136074588	ATTAACACAGACGGA[C/G]AGGTCAAAACCATTC	138151
rs4454361	snp	C/T	0	0	intron-variant, upstream-variant-2KB	NACC2	GRCh38.p7	9:136052544	CAGGCAGTGGGTGGG[C/T]GAGGCGGCACCCCAG	138151
rs4500151	snp	C/G	0.277778	0.248452	intron-variant	NACC2	GRCh38.p7	9:136047135	AGAGACAGCTACCTG[C/G]CTCCACTCCTGCACG	138151
rs4562408	snp	A/G	0.236724	0.249647	intron-variant	NACC2	GRCh38.p7	9:136075365	GAGGCTGGCTGCTGC[A/G]AACTGACTGAAGCGC	138151
rs4601410	snp	A/G	0.237882	0.249706	intron-variant	NACC2	GRCh38.p7	9:136075422	GGCTTGGAACTCGGA[A/G]GCGAATGTCTCCCCG	138151
rs4841905	snp	C/T	0.361053	0.22398	intron-variant	NACC2	GRCh38.p7	9:136020203	GAACAAATGAACGAA[C/T]GTCAGAAGGAGGGGG	138151
rs4841906	snp	A/G	0.434543	0.168653	intron-variant	NACC2	GRCh38.p7	9:136023175	CTCTGGGTCTCCTGG[A/G]AACCCGGATGGAAAG	138151
rs4841907	snp	A/G	0.5	0	intron-variant	NACC2	GRCh38.p7	9:136046087	GGGGCTCCCGCTCAG[A/G]CCACAGCACCACCAA	138151
rs4841908	snp	A/G	0	0	intron-variant, upstream-variant-2KB	NACC2	GRCh38.p7	9:136053757	CTTCGCCCCAAGGAC[A/G]GGGGGGTAGGGATGT	138151
rs4841909	snp	A/G	0.394538	0.203982	intron-variant	NACC2	GRCh38.p7	9:136064874	GACAGACTTAGATCA[A/G]TGGAACAGATGAGTC	138151
rs4841910	snp	A/G	0.413083	0.189483	intron-variant	NACC2	GRCh38.p7	9:136076100	ACAGGCACCCTTCGC[A/G]GCCTCTGCCTGATTT	138151
rs4841911	snp	C/T	0.41325	0.18934	intron-variant	NACC2	GRCh38.p7	9:136076137	CAGTAGTGATGACAC[C/T]CCATACCCCGTGACA	138151
rs4841912	snp	C/T	0.0807149	0.183963	intron-variant	NACC2	GRCh38.p7	9:136077048	agccgggtgtggtgg[C/T]gggcgcctgtagtcc	138151
rs4841913	snp	C/G/T	0.117188	0.211804	intron-variant	NACC2	GRCh38.p7	9:136077050	ccgggtgtggtggcg[C/G/T]gcgcctgtagtccca	138151
rs4841914	snp	C/G	0.0807149	0.183963	intron-variant	NACC2	GRCh38.p7	9:136077063	cgggcgcctgtagtc[C/G]cagccacttgggagg	138151
rs4841915	snp	C/T	0.393065	0.205018	intron-variant	NACC2	GRCh38.p7	9:136077067	cgcctgtagtcccag[C/T]cacttgggaggctga	138151
rs4841916	snp	C/G	0.316726	0.240931	intron-variant	NACC2	GRCh38.p7	9:136077545	CAAAGGGCGTGTGGT[C/G]AGAGTATGGAAAGAA	138151
rs4842070	snp	C/G	0.0879971	0.190408	utr-variant-3-prime	NACC2	GRCh38.p7	9:136007047	CAGTGCCATCCAAAT[C/G]TTCAAGTCAAAAATA	138151
rs4842071	snp	A/G	0.26326	0.249648	utr-variant-3-prime	NACC2	GRCh38.p7	9:136010451	ACTAGTCGCCCACCC[A/G]GGACCCCCTTTTTCC	138151
rs4842072	snp	A/G	0.221439	0.248363	utr-variant-3-prime	NACC2	GRCh38.p7	9:136010746	CACGTCCCACAGTGG[A/G]CCCGGGCGGGACAGT	138151
rs4842073	snp	A/C	0.499996	0.00139776	intron-variant	NACC2	GRCh38.p7	9:136021468	acccccaagtgctgg[A/C]gaggacacggggcag	138151
rs4842074	snp	A/G	0.376791	0.215463	intron-variant	NACC2	GRCh38.p7	9:136021558	gcttggtggcttctt[A/G]tcaagttcaacatac	138151
rs4842075	snp	C/T	0.364609	0.222182	intron-variant	NACC2	GRCh38.p7	9:136021837	CTGTTACACAGAAGA[C/T]GTAAAATGATTACAT	138151
rs4842076	snp	C/T	0.495963	0.0447464	intron-variant	NACC2	GRCh38.p7	9:136021943	CCAGGGGCTGGGGTG[C/T]GGACAAGCCTCAAGG	138151
rs4842077	snp	C/T	0.000399281	0.0141238	intron-variant	NACC2	GRCh38.p7	9:136022757	CAGAAAGACCAGAAA[C/T]GACTTCCACGCTGTA	138151
rs4842078	snp	C/G	0.284209	0.247648	intron-variant	NACC2	GRCh38.p7	9:136028032	tgggaggccaaggtg[C/G]gtggatcacttgagg	138151
rs4842079	snp	G/T	0.498589	0.02652	intron-variant	NACC2	GRCh38.p7	9:136031992	CTGCATAAATGAATG[G/T]GGGGCAAGGGTCGTC	138151
rs4842080	snp	A/T	0.464309	0.12873	intron-variant	NACC2	GRCh38.p7	9:136032177	AAAGGAGGGGAAGGA[A/T]TATCAGCGAGCTGCA	138151
rs4842081	snp	A/T			intron-variant	NACC2	GRCh38.p7	9:136033940	GTGTGTGTGTGTGTG[A/T]GAGATATTTGGCAAT	138151
rs4842083	snp	A/G	0.375	0.216506	intron-variant	NACC2	GRCh38.p7	9:136036983	agataaaagcagcct[A/G]agaagaagacacaat	138151
rs4842084	snp	A/G	0.375399	0.216275	intron-variant	NACC2	GRCh38.p7	9:136043624	GGTCTCACGCACAGG[A/G]ATCCTATGAGAAGCA	138151
rs4842085	snp	C/T			intron-variant	NACC2	GRCh38.p7	9:136045333	TGTGGCCAGAGCTGT[C/T]CCCTGCCAGGAAAGG	138151
rs4842086	snp	C/T			intron-variant	NACC2	GRCh38.p7	9:136045340	AGAGCTGTCCCCTGC[C/T]AGGAAAGGGTTACCG	138151
rs4842087	snp	A/G			intron-variant	NACC2	GRCh38.p7	9:136045341	GAGCTGTCCCCTGCC[A/G]GGAAAGGGTTACCGT	138151
rs4842088	snp	C/T	0.00119737	0.0244387	intron-variant	NACC2	GRCh38.p7	9:136045353	GCCAGGAAAGGGTTA[C/T]CGTCACGGGCCCACG	138151
rs4842089	snp	A/G			intron-variant	NACC2	GRCh38.p7	9:136045417	AGGGTTACCGTGGAA[A/G]TGTGCAGCTGGTGTC	138151
rs4842090	snp	A/C	0.489796	0.070696	intron-variant	NACC2	GRCh38.p7	9:136049080	TCTCCAATTAGGGCA[A/C]CCTGGGTTTGTGGGG	138151
rs4842091	snp	A/G	0.378372	0.214524	intron-variant	NACC2	GRCh38.p7	9:136055321	AAGGACACAGGTTAC[A/G]AGGTTGGTGCCAGGC	138151
rs4842092	snp	A/G	0.481932	0.0933148	intron-variant	NACC2	GRCh38.p7	9:136055860	GTGAGGACATCTCCT[A/G]AAAGGTCAATCGAAG	138151
rs4842093	snp	A/T	0.427727	0.175821	intron-variant	NACC2	GRCh38.p7	9:136055985	AGTCTGGGGGCTGCT[A/T]CCCCGTGGACCTTGC	138151
rs4842095	snp	C/G	0.29278	0.246313	intron-variant	NACC2	GRCh38.p7	9:136057028	CCCAGCCCCCACCCC[C/G]AGGGTGGGCCTCCAG	138151
rs4842096	snp	A/G	0.294832	0.245947	intron-variant	NACC2	GRCh38.p7	9:136064784	TTAAAAAAGAGGAGC[A/G]AAGTTAGAGCAGTCA	138151
rs4842097	snp	A/G	0.41023	0.191902	intron-variant	NACC2	GRCh38.p7	9:136067844	tctcaaaaacacaga[A/G]acaaaaccaaagcca	138151
rs4842098	snp	A/T	0.231111	0.249285	intron-variant	NACC2	GRCh38.p7	9:136072256	aaagaaaaaaaaaaa[A/T]acccaaaggcagggc	138151
rs4842099	snp	C/T	0.21875	0.248039	intron-variant	NACC2	GRCh38.p7	9:136075689	GCTCCCTGTGCCCGG[C/T]CTTCCACACGCGGGG	138151
rs4842100	snp	A/G	0.155325	0.23138	intron-variant	NACC2	GRCh38.p7	9:136076140	TAGTGATGACACCCC[A/G]TACCCCGTGACATCC	138151
rs4842101	snp	A/G	0.41325	0.18934	intron-variant	NACC2	GRCh38.p7	9:136076182	TATGCAACCAAAAGA[A/G]AAGCAAATGATTTCC	138151
rs4842102	snp	C/T	0.396	0.202938	intron-variant	NACC2	GRCh38.p7	9:136076351	GAGCCAGGTTTCCTG[C/T]CCATACCACGACAAA	138151
rs4842103	snp	C/T	0.481319	0.0948228	intron-variant	NACC2	GRCh38.p7	9:136076541	CAGGGGCTGGGGGAC[C/T]GCGGAGGGGAGTTGG	138151
rs4842104	snp	C/T	0.404559	0.196498	intron-variant	NACC2	GRCh38.p7	9:136076697	GAATTTCATGTTGTG[C/T]ATATTTGACTACAAT	138151

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