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
rs7398	snp	A/G	0.468098	0.122202	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505817	ACTCATGGGGGCTTA[A/G]GATGCAGCTACCTCA	113878
rs723378	snp	C/T	0	0	intron-variant	DTX2	GRCh38.p7	7:76486163	GCACGAGCCTATCTA[C/T]GCGCTGAAAAACAGG	113878
rs723380	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76486232	TTAACCCTCCTCTGA[C/T]GGATGTAGAGCCAGA	113878
rs880777	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477886	ACCttgagttattca[A/G]ccaaggtcacacata	113878
rs887044	snp	C/T	0.499325	0.0183582	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479395	GGTGCCCTGAAGCAT[C/T]GCTAACCAAAAAGGA	113878
rs917425	snp	C/G	0.473818	0.111381	intron-variant	DTX2	GRCh38.p7	7:76500368	AGAGGGCGAGGAAGG[C/G]AAGGAAGAGGTCTAA	113878
rs1010933	snp	C/T	0	0	synonymous-codon	DTX2	GRCh38.p7	7:76505502	AGAGATGGACCGCAA[C/T]ATTACGGGCCACGGC	113878
rs1051646	snp	A/G			utr-variant-3-prime	DTX2	GRCh38.p7	7:76505906	GGTGTGGGGCGAGTA[A/G]AGACTTCCCCAGCCT	113878
rs1055094	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474928	CGTCAGGTCTTCGCC[A/G]CAAATCTCTGTCCAG	113878
rs1055096	snp	A/C	0.330714	0.236612	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474864	GTTCTACTGGAGATG[A/C]AATTTCATCCAAAAG	113878
rs1465314	snp	A/C	0.422158	0.181278	intron-variant	DTX2	GRCh38.p7	7:76504886	GCTCTACCCCTGGTG[A/C]TGGCCTGGGGGGCAC	113878
rs1467939	snp	C/T	0	0	intron-variant	DTX2	GRCh38.p7	7:76465462	ACTAACGTTCTGATC[C/T]TGTCTTTTACACACC	113878
rs1476932	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76467189	tagacatgagccacc[A/G]tgctcggcAGTGTTC	113878
rs1476934	snp	A/G	0	0	intron-variant	DTX2	GRCh38.p7	7:76467384	TCCCTGAGCCCtgct[A/G]ctgaatatctcctct	113878
rs1476935	snp	C/T	0	0	intron-variant	DTX2	GRCh38.p7	7:76467897	ATTCTCAGTGGGGGA[C/T]GAAGGGCATGAAACA	113878
rs1548823	snp	A/G	0	0	utr-variant-3-prime	DTX2	GRCh38.p7	7:76505626	GCGGGGTGGCCACCA[A/G]AGGCGGGCGTGCTGG	113878
rs1613849	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76469017	AGCACTTCGGGAGGC[C/T]GAGGTGGGTGGATCA	113878
rs1614739	snp	C/T	0.5	0	intron-variant	DTX2	GRCh38.p7	7:76492403	CTCACTCTGGGGTGA[C/T]ACCATCACCAGAAAG	113878
rs1616563	snp	A/G	0	0	intron-variant	DTX2	GRCh38.p7	7:76469425	agcttgggcgacaga[A/G]tgagaatccgtctca	113878
rs1621319	snp	C/G	0.5	0	intron-variant	DTX2	GRCh38.p7	7:76499600	GGGACGGGGAGCCCA[C/G]TGCCACCCGTGGAGG	113878
rs1622742	snp	A/G	0.491936	0.0629843	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476021	GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCGC	113878
rs1623251	snp	A/C/T	0.0541011	0.15593	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475226	CCTCCCGGGTTCAAG[A/C/T]GATTCTTCTGCCTCA	113878
rs1627895	snp	A/G	0.483995	0.0880135	intron-variant	DTX2	GRCh38.p7	7:76481979	TGGGCATGACGGCTC[A/G]AGCCTGTAATCCCAA	113878
rs1628199	snp	C/T	0.483923	0.0882034	intron-variant	DTX2	GRCh38.p7	7:76481251	tgcagtgagccgaga[C/T]tgcgccactgcactc	113878
rs1628255	snp	C/T	0.483923	0.0882034	intron-variant	DTX2	GRCh38.p7	7:76481232	gccactgcactccag[C/T]ttaggcaacagagcc	113878
rs1631301	snp	A/C			intron-variant, utr-variant-5-prime	DTX2	GRCh38.p7	7:76462005	CCGATCCCCCCGACA[A/C]CCCCGATCTCCCGGG	113878
rs1631425	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76488820	ACCTCTCTGCCTCCC[A/G]GGCTCAAGCAATTCT	113878
rs1638067	snp	C/G	0	0	intron-variant	DTX2	GRCh38.p7	7:76487571	TGAGCATGGCAAGTC[C/G]CCTTCCCGAGCCTCA	113878
rs1638072	snp	C/T	0.498206	0.0298983	intron-variant	DTX2	GRCh38.p7	7:76484014	GCTGAAGTGCAGTGG[C/T]GCGATCACAGCTCAC	113878
rs1638073	snp	C/T	0.351492	0.228472	intron-variant	DTX2	GRCh38.p7	7:76483170	ACAGGGCAGACAAAA[C/T]GAGCGGCCGTTGCCC	113878
rs1638074	snp	A/G	0.495992	0.0445839	synonymous-codon	DTX2	GRCh38.p7	7:76482743	CCGCACGCTGCGGCA[A/G]AAGCTGGAAGTCTTG	113878
rs1638075	snp	C/G	0.308133	0.243155	synonymous-codon	DTX2	GRCh38.p7	7:76482677	GTTGTACCCCAGGGG[C/G]GCCAAGTCCACGAGC	113878
rs1638076	snp	C/G	0.483923	0.0882034	intron-variant	DTX2	GRCh38.p7	7:76482215	ATGACACCACACCCA[C/G]CTAACTTCAAATCGA	113878
rs1638077	snp	A/T	0	0	intron-variant	DTX2	GRCh38.p7	7:76500971	TGATCACGCCACTGC[A/T]CTGAGCCTGGGCGAC	113878
rs1638081	snp	A/G	0.486464	0.0811471	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476871	CCCAATGGAGGGCGC[A/G]CCATGGCCCAGGCCC	113878
rs1638082	snp	A/G	0.5	0	intron-variant	DTX2	GRCh38.p7	7:76498716	CCCCAGCTCAGGGTC[A/G]CCCTCCGTGTGGCTG	113878
rs1638083	snp	C/G	0.485187	0.0847778	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76474507	CCTGCCTCTGCCGTC[C/G]CGAGAGAAGATGAAA	113878
rs1638084	snp	C/T			intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76473898	CACAGAAATGTGGGA[C/T]GTTGTTTTTGACACA	113878
rs1638085	snp	C/T	0.5	0	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76473574	caagtgatctgccca[C/T]ctcggtctcctcaag	113878
rs1638086	snp	C/T	0.462582	0.131564	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472903	CTAACTTCAGAAAAT[C/T]ATAGAAAAATTTTGA	113878
rs1638087	snp	C/T	0.332106	0.236133	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472382	CCGAGAACTGCACCA[C/T]TGCACTCCAGCCTGG	113878
rs1638088	snp	G/T	0.456214	0.141336	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472323	AAAACAAACCTCCCT[G/T]AAAATGCCAAACACT	113878
rs1638089	snp	C/T	0.375	0.216506	intron-variant, utr-variant-5-prime, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76470409	ATTACCTTGACTTCT[C/T]TGGGGACCCCAGTGT	113878
rs1638091	snp	A/G	0.4032	0.19756	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76470159	GGGCAGGGGCTCTGC[A/G]TACTATTCGATGAGA	113878
rs1638094	snp	A/G	0.486984	0.079614	intron-variant	DTX2	GRCh38.p7	7:76469133	TAGACCACAAGAACA[A/G]CCATAAACAATGTGT	113878
rs1638095	snp	A/G	0.491368	0.0651254	intron-variant	DTX2	GRCh38.p7	7:76469051	GGGGCTGAATGCGGT[A/G]GCTCACGCCTGTAAT	113878
rs1638096	snp	C/T	0.212425	0.24716	intron-variant	DTX2	GRCh38.p7	7:76468832	gaggctgcagtgagc[C/T]gagactgtgccactg	113878
rs1638101	snp	C/T	0.496616	0.0409947	intron-variant	DTX2	GRCh38.p7	7:76465227	CCCCATGACTCTGCT[C/T]CACCCTGAATCCCAC	113878
rs1638102	snp	A/G	0.362732	0.22314	intron-variant	DTX2	GRCh38.p7	7:76497540	CTGTGCAGAAGAGTC[A/G]GAGGCAGCGAGGCCG	113878
rs1638103	snp	C/T	0.5	0	intron-variant	DTX2	GRCh38.p7	7:76464245	GACTCCTCTCCCAGG[C/T]GACTGTGCCCCACTT	113878
rs1638119	snp	A/G	0	0	intron-variant	DTX2	GRCh38.p7	7:76495842	CGGCAACACTGCCTC[A/G]GCGGGCAGGCCTTCC	113878
rs1638120	snp	C/G	0.305186	0.243833	intron-variant	DTX2	GRCh38.p7	7:76500642	CCAAAGGGGCTGGAG[C/G]AAGGCCCTGGCACCC	113878
rs1638150	snp	A/G	0.375	0.216506	intron-variant	DTX2	GRCh38.p7	7:76494327	ACGGTGACTTCAGTG[A/G]GCAGGGACTTTCTGG	113878
rs1638151	snp	C/G	0.5	0	intron-variant	DTX2	GRCh38.p7	7:76493860	CTGCTCCTCAGTTGT[C/G]ACTGGCTGCACTCCA	113878
rs1638153	snp	C/T	0.277778	0.248452	intron-variant	DTX2	GRCh38.p7	7:76493649	CCCTCTCAGCCACTA[C/T]GACAGCAACTCCCCT	113878
rs1638154	snp	C/T	0.451359	0.148171	intron-variant	DTX2	GRCh38.p7	7:76492052	GGAGTCACTGAGGTG[C/T]CTTCGCGCTTTTACG	113878
rs1638155	snp	C/T	0.493748	0.0555599	intron-variant	DTX2	GRCh38.p7	7:76491615	AAAAAAGATATTTTA[C/T]ACTCACTAGTGTCAT	113878
rs1799127	snp	C/T	0.465683	0.126415	intron-variant	DTX2	GRCh38.p7	7:76498537	GAAAGCTCCCTTCTG[C/T]TCTGAAAAGCTGCAA	113878
rs1799148	snp	C/G	0	0	intron-variant	DTX2	GRCh38.p7	7:76494959	GCGTTTGCGCACAGG[C/G]TTTTTGCAGAGAGGT	113878
rs1799157	snp	C/T	0.277778	0.248452	intron-variant	DTX2	GRCh38.p7	7:76488741	TCTCTACTAAAAATA[C/T]AAAAATTAGCCAGGC	113878
rs1799158	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76488789	TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	113878
rs1799161	snp	A/G	0.375	0.216506	intron-variant	DTX2	GRCh38.p7	7:76496909	TGGAGCACACACAGC[A/G]CCCAGTGGAGGCTGG	113878
rs1799163	snp	A/T			intron-variant	DTX2	GRCh38.p7	7:76485555	TCCCTGAGCCTGGCT[A/T]GCCTATGTCTATGTC	113878
rs1799167	snp	C/T	0.5	0	intron-variant	DTX2	GRCh38.p7	7:76484582	TCCCTGGGACCAGGG[C/T]GGCCCCAGGCCCACC	113878
rs1799169	snp	A/G	0.498852	0.0239341	intron-variant	DTX2	GRCh38.p7	7:76484046	TTAAGACAGGGTCTC[A/G]CTCTGTCACCTAGGG	113878
rs1799171	snp	A/G	0.408163	0.193609	intron-variant	DTX2	GRCh38.p7	7:76483385	AGGCCCTTAATCATC[A/G]TGAGTGAAAGGACTG	113878
rs1799172	snp	G/T	0.451359	0.148171	intron-variant	DTX2	GRCh38.p7	7:76497754	TTTTGTAAGCAACAA[G/T]TTGTGGGTGAGAGGC	113878
rs1799173	snp	C/G	0.485049	0.0851591	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76480273	CTCTCACCCAGGCTA[C/G]AGTGCAGCAGTGTGA	113878
rs1799178	snp	C/T			intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479710	GCAACCTCCACCTCC[C/T]GGGTAGGTTCAAGTG	113878
rs1799179	snp	A/T	0.467439	0.123371	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76479610	gtatttttagtagag[A/T]cggggtttcaccatg	113878
rs1799182	snp	C/T	0.466204	0.125522	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76478687	GGTGGCTCACACCTG[C/T]AATGCCAGTGTTTAG	113878
rs1799183	snp	C/T	0	0	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477728	ACTGCAGCCCCATGG[C/T]CTCCTGGGCTAAAGC	113878
rs1799186	snp	A/G	0.485933	0.0826777	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477244	GGCAGCTCTGTGGGT[A/G]CCAGGCCCGCCACGG	113878
rs1799187	snp	A/G	0.485866	0.0828688	intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477235	GTGGGTGCCAGGCCC[A/G]CCACGGAGCTGCCAA	113878
rs1799188	snp	C/T	0.49703	0.0384237	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476872	CCCCAATGGAGGGCG[C/T]ACCATGGCCCAGGCC	113878
rs1799189	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76476402	TGAGCCTTCTGCTCC[A/G]GGGGCACAGGCACCT	113878
rs1799191	snp	A/G	0.5	0	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472035	GCCAGTGCCTCCCAC[A/G]TCTTACTGGAAGATG	113878
rs1799192	snp	A/G	0.375	0.216506	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471322	TACAAAAAATTAGCC[A/G]GGCGCGGTGGCGGGT	113878
rs1799193	snp	A/T	0.375	0.216506	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76471287	GTAGTCCCGGCTACT[A/T]GGGAGGCTGAGGCAG	113878
rs1799196	snp	A/T	0.49703	0.0384237	intron-variant	DTX2	GRCh38.p7	7:76467241	ACTGGTATAAGCACT[A/T]CATTCAGGAAATGGT	113878
rs1799197	snp	A/G			intron-variant	DTX2	GRCh38.p7	7:76465673	GAATCACTTGAACCC[A/G]GGAGGTGGAGGTTGC	113878
rs1799198	snp	A/G	0.442791	0.15916	intron-variant	DTX2	GRCh38.p7	7:76465471	GCTTCCTGAACTAAC[A/G]TTCTGATCTTGTCTT	113878
rs1799200	snp	A/G	0	0	intron-variant	DTX2	GRCh38.p7	7:76464698	TAAAATGTCCCTCAC[A/G]AGGCCAGGCACGGTG	113878
rs1799201	snp	A/G	0.495818	0.0455352	intron-variant	DTX2	GRCh38.p7	7:76464421	TAAAATGACCCTCAT[A/G]GAAATCTCCTAAAAT	113878
rs1799202	snp	C/G	0.4982	0.0299459	upstream-variant-2KB	DTX2	GRCh38.p7	7:76461569	AGGCGCACCTGCTCC[C/G]GTCTATGTTTTCTTC	113878
rs1799203	snp	A/G	0.46875	0.121031	upstream-variant-2KB	DTX2	GRCh38.p7	7:76459774	CAGGATCTGAGGAGT[A/G]TGGGGAGAAGCCGGG	113878
rs1978294	snp	C/T	0.420255	0.183066	intron-variant	DTX2	GRCh38.p7	7:76503060	GACACTAGGGAAGGC[C/T]GAGCCAGGCTCCGAT	113878
rs2005531	snp	A/G			intron-variant, upstream-variant-2KB	DTX2	GRCh38.p7	7:76477757	gtgagtggtgattgc[A/G]gccactgcactctag	113878
rs2257223	snp	C/G	0.449345	0.150869	intron-variant, utr-variant-3-prime	DTX2	GRCh38.p7	7:76501515	TCCCTGCCTGGAACC[C/G]CCAGCAGGACCCCCA	113878
rs2258205	snp	A/G			intron-variant, upstream-variant-2KB	DTX2, FDPSP2	GRCh38.p7	7:76475676	tggcgacagagcaag[A/G]ctccttctcaaaaat	113878
rs2258686	snp	A/C/G	0.212077	0.24714	synonymous-codon	DTX2	GRCh38.p7	7:76482932	CCCCCAGCACCCCCC[A/C/G]CACAGGACCGCTTCT	113878
rs2258855	snp	A/C	0.497933	0.032082	intron-variant	DTX2	GRCh38.p7	7:76489896	TCATATTAAAAAAAA[A/C]AAAAACAACAACCTT	113878
rs2259255	snp	A/G	0.000399281	0.0141238	intron-variant	DTX2	GRCh38.p7	7:76482069	GTCAGCTCCCAAGTC[A/G]TTGCCTTCACAGTGT	113878
rs2260214	snp	C/T	0.5	0	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502136	AAGTGATCGGCCTCC[C/T]AGAGTGCTGGGATTA	113878
rs2260306	snp	C/G	0.0210502	0.100409	intron-variant	DTX2	GRCh38.p7	7:76504466	TGCCACCATGCGCCC[C/G]GGGGGTGGACGGGGC	113878
rs2260344	snp	C/T			intron-variant	DTX2	GRCh38.p7	7:76481620	CAATGTTTGGAGACA[C/T]TGTTGGTTGTT	113878
rs2261368	snp	C/G	0.5	0	intron-variant, downstream-variant-500B	DTX2	GRCh38.p7	7:76502011	CTTGCCTCAGCCTCC[C/G]GAGTAGCTGGGATTA	113878
rs2261681	snp	A/G	0.5	0	intron-variant	DTX2	GRCh38.p7	7:76466631	agtttcactcttatt[A/G]cctaggctggagtgc	113878
rs2261946	snp	C/T	0.5	0	intron-variant, nc-transcript-variant	DTX2, FDPSP2	GRCh38.p7	7:76472447	TTCTCCTGCCTCAGC[C/T]TCCCAGGTAGCTGGG	113878
rs2262041	snp	C/G	0.5	0	intron-variant	DTX2	GRCh38.p7	7:76500047	TTGAATCAAATCGTG[C/G]TGCCACAACGCCCCC	113878

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