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
rs1128757	snp	A/G	0.207253	0.246318	upstream-variant-2KB, intron-variant, nc-transcript-variant	RNF139, RNF139-AS1	GRCh38.p7	8:124472960	GGCCATTATGGGGAA[A/G]AAGATCCAAAAGGAC	11236
rs1128758	snp	A/C	0	0	upstream-variant-2KB, intron-variant, nc-transcript-variant	RNF139, RNF139-AS1	GRCh38.p7	8:124472868	AAATGAGTTCATGGG[A/C]TTTCCTCtaattttt	11236
rs1128760	snp	A/T	0	0	upstream-variant-2KB, intron-variant, nc-transcript-variant	RNF139, RNF139-AS1	GRCh38.p7	8:124472867	AATGAGTTCATGGGC[A/T]TTCCTCtaattttta	11236
rs1129066	snp	C/T	0	0	utr-variant-3-prime	RNF139	GRCh38.p7	8:124487820	ATACCTCTTTAATTA[C/T]TTCTGGTCTCTTTGG	11236
rs3812471	snp	A/G	0.4999	0.00706081	synonymous-codon	RNF139	GRCh38.p7	8:124486306	CAATAACTGTAATCC[A/G]TAAATTCGATACATG	11236
rs3812472	snp	C/T	0.490673	0.0676508	upstream-variant-2KB, nc-transcript-variant	RNF139, RNF139-AS1	GRCh38.p7	8:124474526	CTTCACCCTCGCAGA[C/T]TCGGCTTAGCGAGCG	11236
rs4330675	snp	C/T	0.169435	0.236663	intron-variant	RNF139	GRCh38.p7	8:124476666	TAACGTATACCACCA[C/T]CATAATTTGTGTTAA	11236
rs4366064	snp	A/C			intron-variant	RNF139	GRCh38.p7	8:124477973	GAATCCTTAAATGAC[A/C]AACTGAGATAAAATA	11236
rs4551335	snp	A/G	0.211516	0.24702	intron-variant	RNF139	GRCh38.p7	8:124481701	CTCAAAATTTTTTAT[A/G]AAGCAGCATTTATAT	11236
rs4870899	snp	A/C	0.257732	0.24988	intron-variant, upstream-variant-2KB	RNF139, RNF139-AS1	GRCh38.p7	8:124476086	GTAATTGTAACTTGG[A/C]AAATTTTGTTGATGA	11236
rs4871493	snp	C/G	0.259674	0.249813	intron-variant	RNF139	GRCh38.p7	8:124482681	CCTATAATCGCAGTA[C/G]TTTGGGAGGCCGAAG	11236
rs6997089	snp	A/G	0.16911	0.236552	intron-variant, downstream-variant-500B	TATDN1, RNF139	GRCh38.p7	8:124488792	AAGGAAAATATTGGC[A/G]CACCTTTAATATAAT	11236
rs6997843	snp	C/T	0.207253	0.246318	upstream-variant-2KB, intron-variant, downstream-variant-500B	RNF139, RNF139-AS1	GRCh38.p7	8:124472786	GGGACAGTTAAAACA[C/T]TAATAAAGACTGAAG	11236
rs9969474	snp	G/T	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	RNF139, RNF139-AS1	GRCh38.p7	8:124476321	GCAAAGCATTTTCAC[G/T]GGTAGgtattatcta	11236
rs10956185	snp	G/T	0.209084	0.246629	upstream-variant-2KB, intron-variant	RNF139, RNF139-AS1	GRCh38.p7	8:124473487	ACAAGGTAGTAACCT[G/T]GTCATCTTGTAACTT	11236
rs10956186	snp	G/T	0.168785	0.236441	intron-variant	RNF139	GRCh38.p7	8:124483609	TGGCATATTTTTATA[G/T]TTTTGGTAGAGACAG	11236
rs11354778	in-del	-/A	0.19334	0.243495	intron-variant	RNF139	GRCh38.p7	8:124480140	AAGACCCTGTCTCTT[-/A]AAAAAAAAAAATAGT	11236
rs11778396	snp	C/G	0.371177	0.218669	intron-variant, upstream-variant-2KB	RNF139, RNF139-AS1	GRCh38.p7	8:124475525	ACCTGAGTGAGGTGG[C/G]GAGAAAGTAAGGATG	11236
rs13250890	snp	G/T	0.127599	0.217986	intron-variant	RNF139	GRCh38.p7	8:124483467	GTAttttgagacagg[G/T]tctcactgtcaccca	11236
rs13254054	snp	G/T	0.108048	0.20579	intron-variant	RNF139	GRCh38.p7	8:124478543	aatcggggaggtgga[G/T]gttgcagtgagccaa	11236
rs13254069	snp	G/T			intron-variant	RNF139	GRCh38.p7	8:124478565	gtgagccaagatcgc[G/T]ccactgcactccagc	11236
rs13264071	snp	A/G	0.20111	0.245173	intron-variant, utr-variant-3-prime, downstream-variant-500B	TATDN1, RNF139	GRCh38.p7	8:124488277	ACCAGAATGTGCTAA[A/G]TGTTTTTTATGTAAA	11236
rs13278060	snp	A/C	0.00557542	0.0525036	intron-variant	RNF139	GRCh38.p7	8:124485762	TTAAAGGAAGAATAT[A/C]ATAACTCTTAGTGGG	11236
rs28414531	snp	C/T	0.00557542	0.0525036	intron-variant	RNF139	GRCh38.p7	8:124481423	TATGAATAGACTTTA[C/T]ACATAAAAGAGTGAA	11236
rs28465300	snp	C/T	0.00517822	0.0506191	upstream-variant-2KB, intron-variant	RNF139, RNF139-AS1	GRCh38.p7	8:124474082	CTGTCCAGGTGTACT[C/T]ACCTCAAAGATGAGA	11236
rs28519972	snp	A/C			intron-variant	RNF139	GRCh38.p7	8:124480315	AATGAAGATTGATAA[A/C]CCGAATGATATTGAG	11236
rs28536724	snp	A/T			intron-variant	RNF139	GRCh38.p7	8:124482959	ATATATATATATATA[A/T]TATATATATATTATT	11236
rs28549965	snp	A/T	0.20111	0.245173	intron-variant	RNF139	GRCh38.p7	8:124482943	AAAAATATAAAAAAA[A/T]ATATATATATATATA	11236
rs28635338	snp	A/T	0.02016	0.0983543	intron-variant	RNF139	GRCh38.p7	8:124482941	AAAAAAATATAAAAA[A/T]AAATATATATATATA	11236
rs28642883	snp	A/G	0.00557542	0.0525036	upstream-variant-2KB	RNF139, RNF139-AS1	GRCh38.p7	8:124474565	CCAACGCCGGAAAGC[A/G]CGGCTACCGAAAAGC	11236
rs28704640	snp	A/T			intron-variant	RNF139	GRCh38.p7	8:124482960	TATATATATATATAA[A/T]ATATATATATTATTT	11236
rs34085156	snp	A/G	0.00199352	0.0315085	synonymous-codon	RNF139	GRCh38.p7	8:124486975	TCTCACTGTTTATAC[A/G]TTATTCATGATTGAT	11236
rs34191543	snp	A/C	0.0253123	0.109615	missense, synonymous-codon	RNF139	GRCh38.p7	8:124486900	TCACTATGCACTAAA[A/C]ACATGGTTGTTTGCA	11236
rs34202779	in-del	-/C			intron-variant	RNF139	GRCh38.p7	8:124476974	TTGTGTTTGACAAAG[-/C]AACAACATGACTTAA	11236
rs34561070	in-del	-/C			frameshift-variant	RNF139	GRCh38.p7	8:124486454	ATTCCTTCTTTATTT[-/C]CTTGGGATGATTTTT	11236
rs34627465	in-del	-/C			upstream-variant-2KB, nc-transcript-variant	RNF139, RNF139-AS1	GRCh38.p7	8:124474147	TCAGTCGCTATCTCC[-/C]TTGCCATTAGTAAAA	11236
rs34661621	in-del	-/A	0	0	intron-variant	RNF139	GRCh38.p7	8:124480426	CGAGACTCCATCACT[-/A]AAAAAAAAAAAAAAA	11236
rs34681911	in-del	-/G			frameshift-variant	RNF139	GRCh38.p7	8:124486457	CCTTCTTTATTTCTT[-/G]GGGATGATTTTTGGG	11236
rs35051122	in-del	-/C			upstream-variant-2KB, nc-transcript-variant, intron-variant	RNF139, RNF139-AS1	GRCh38.p7	8:124474223	GGAAGGGTGACGTGC[-/C]AAATGGATGGGAGGA	11236
rs35331885	in-del	-/T			upstream-variant-2KB, intron-variant	RNF139, RNF139-AS1	GRCh38.p7	8:124473691	AGCAGTAAGGACTTT[-/T]GGGTGGGGATTCGGT	11236
rs35419095	snp	A/G	0.126909	0.217598	intron-variant	RNF139	GRCh38.p7	8:124477859	ATTGAGGTGGGAAAA[A/G]GCTTTAAACATAACA	11236
rs35604899	in-del	-/C			intron-variant	RNF139	GRCh38.p7	8:124476788	TTCTGTGAGAATCCC[-/C]TTTGGGACCTGGTGC	11236
rs35849960	in-del	-/AAGT	0.190117	0.242722	intron-variant, downstream-variant-500B	TATDN1, RNF139	GRCh38.p7	8:124488824	TAACAGTTATTAAGT[-/AAGT]TTTTCAGCAATATCA	11236
rs35910379	in-del	-/T			intron-variant	RNF139	GRCh38.p7	8:124482233	GCACTTTTTCACTAG[-/T]AAATGTTTCTAAAAC	11236
rs35970900	snp	A/G	0.192841	0.243378	missense	RNF139	GRCh38.p7	8:124486332	TATTGATGGAGGACA[A/G]ATGGAAGAGGATTCG	11236
rs36072676	snp	C/G/T	0.000115324	0.00759268	synonymous-codon, utr-variant-5-prime	RNF139	GRCh38.p7	8:124485988	CTACAACACGTCAGC[C/G/T]TTTGGAATTGAGCTG	11236
rs56714947	snp	A/T			intron-variant	RNF139	GRCh38.p7	8:124482972	TAATATATATATATT[A/T]TTTAAATATATATAT	11236
rs56946240	snp	A/T	0.207253	0.246318	upstream-variant-2KB, intron-variant	RNF139, RNF139-AS1	GRCh38.p7	8:124473562	AGCCGATGAAAAGAT[A/T]GAAGTAAAACATAAA	11236
rs62527885	snp	A/G	0.0023933	0.0345097	intron-variant	RNF139	GRCh38.p7	8:124479679	GTGACAGCCAAAACT[A/G]TCCCTGGATATTGCC	11236
rs62527886	snp	C/T	0.208474	0.246527	intron-variant	RNF139	GRCh38.p7	8:124481298	AGGTATTGAAATGTT[C/T]TTCCACAGGTTGCTT	11236
rs71289669	in-del	-/TA	0	0	intron-variant	RNF139	GRCh38.p7	8:124482958	ATATATATATATATA[-/TA]ATATATATATATTAT	11236
rs71916440	in-del	-/C			intron-variant	RNF139	GRCh38.p7	8:124483053	TATTTAAAAATATAT[-/C]TATTAAAAATATATA	11236
rs72492813	in-del	-/AAAAA			intron-variant	RNF139	GRCh38.p7	8:124483007	AAAAATATATATATT[-/AAAAA]TATATATATATATTT	11236
rs72713050	snp	A/C			upstream-variant-2KB, intron-variant	RNF139, RNF139-AS1	GRCh38.p7	8:124473018	AGGGCAGAATAACAG[A/C]TATGTTGAGTAGCTA	11236
rs72713051	snp	G/T	0.0182019	0.0936463	upstream-variant-2KB, nc-transcript-variant, intron-variant	RNF139, RNF139-AS1	GRCh38.p7	8:124474208	ATCTGGGCAGGAGGT[G/T]GGAAGGGTGACGTGC	11236
rs72713053	snp	G/T	0.167484	0.23599	intron-variant, upstream-variant-2KB	RNF139, RNF139-AS1	GRCh38.p7	8:124475452	TGGGAGGGGGAAGGA[G/T]ATGATACTTGTCTGA	11236
rs72713055	snp	C/G	0.169435	0.236663	intron-variant	RNF139	GRCh38.p7	8:124478310	AAAAAAGTACCTAGC[C/G]TTGTTTATAATTAAA	11236
rs72713059	snp	C/T	0.0879971	0.190408	intron-variant	RNF139	GRCh38.p7	8:124481374	TGTTTTGTACCCTGA[C/T]TTTTAGTCATAAGTT	11236
rs72713064	snp	C/T	0.259674	0.249813	intron-variant	RNF139	GRCh38.p7	8:124483983	TAATAGGGTAGATTA[C/T]ACTTAGATAACTGCA	11236
rs72713066	snp	A/G	0.182552	0.24073	synonymous-codon	RNF139	GRCh38.p7	8:124487122	TATGATGTTTGAGTC[A/G]GGAAGTAAAATTCGG	11236
rs74741031	snp	A/T	0.00874735	0.0655527	intron-variant	RNF139	GRCh38.p7	8:124484111	GATAGGTAGGATTTG[A/T]ATAGTCAGGGATTGG	11236
rs74888846	snp	A/C	0.00318978	0.0398085	intron-variant	RNF139	GRCh38.p7	8:124480119	AGCCTGGCTGGGTGA[A/C]AGAGCAAGACCCTGT	11236
rs74918331	snp	A/G	0.00478085	0.0486577	upstream-variant-2KB, intron-variant	RNF139, RNF139-AS1	GRCh38.p7	8:124473004	TTTACAGTGCAATCA[A/G]GGCAGAATAACAGAT	11236
rs75026028	snp	A/T	0.5	0	intron-variant	RNF139	GRCh38.p7	8:124480404	GCGAGACTCCATCAC[A/T]AAAAAAAAAAAAAAA	11236
rs75049989	snp	C/G	0.00318978	0.0398085	intron-variant	RNF139	GRCh38.p7	8:124484072	CTGAAAGAACAGTTT[C/G]TATCAAAGAAAGTAG	11236
rs75512978	snp	A/T	0.000798403	0.0199641	intron-variant	RNF139	GRCh38.p7	8:124484599	AAGTCGAGTTTCAGA[A/T]CTTTGGAGATTTGCA	11236
rs75798431	snp	C/T	0.00517822	0.0506191	intron-variant	RNF139	GRCh38.p7	8:124476821	TAATGCAGTAGTCTG[C/T]TGAGCTTCAGGTTAG	11236
rs76014606	snp	A/C	0.0012906	0.0253699	synonymous-codon	RNF139	GRCh38.p7	8:124487528	GCTGCTGAATCTGAC[A/C]GGGAATTGAACGAAG	11236
rs76077008	snp	A/T	0	0	intron-variant	RNF139	GRCh38.p7	8:124480409	ACTCCATCACTAAAA[A/T]AAAAAAAAAAAAAAA	11236
rs76904799	snp	A/T	0.5	0	intron-variant	RNF139	GRCh38.p7	8:124483091	TTTAAATATATATAT[A/T]TTTAAAAATATATAT	11236
rs77023890	snp	C/T	0.00874735	0.0655527	upstream-variant-2KB	RNF139, RNF139-AS1	GRCh38.p7	8:124474616	CGAAGCTAGAGTAAG[C/T]TGAGGAGGTGGGCGG	11236
rs77185225	snp	G/T	0.0111196	0.0737302	intron-variant	RNF139	GRCh38.p7	8:124480928	TAATATTTTTTTTAT[G/T]ATATCACAGATGGGA	11236
rs77481784	snp	G/T	0.0248432	0.108648	intron-variant	RNF139	GRCh38.p7	8:124482403	GTTGACAAAAATAAT[G/T]TACAGTTCCTGCTTG	11236
rs77622296	snp	C/T	0.0225045	0.103662	intron-variant	RNF139	GRCh38.p7	8:124483724	TGTGAGCCACCACAC[C/T]CAGCCAAGATGGATT	11236
rs77877010	snp	A/G	0.00199481	0.0315187	intron-variant	RNF139	GRCh38.p7	8:124484255	GAGGAATATTACTGT[A/G]AAGCAAATTGGGTTC	11236
rs78078209	snp	G/T	0.00597247	0.0543191	intron-variant	RNF139	GRCh38.p7	8:124484404	AAGATGAGGGTTTTT[G/T]GAGACAGACTGATTG	11236
rs78303573	snp	A/C			intron-variant	RNF139	GRCh38.p7	8:124479587	GGGAGCTCTCCTGTG[A/C]ACTGTAAGATTTTTA	11236
rs78996314	snp	A/G	0.0271762	0.113356	intron-variant	RNF139	GRCh38.p7	8:124485551	GAAAATAATTTAGTA[A/G]TTTGGTGCCTTGGAC	11236
rs79338669	snp	C/T	0.00290947	0.0380299	synonymous-codon	RNF139	GRCh38.p7	8:124487539	TGACAGGGAATTGAA[C/T]GAAGATGACAGTACA	11236
rs79552291	snp	A/T	0.444444	0.157135	intron-variant	RNF139	GRCh38.p7	8:124483098	ATATATATATTTAAA[A/T]ATATATATATTAAAA	11236
rs79586564	snp	C/G	0.0123036	0.0774623	intron-variant, upstream-variant-2KB	RNF139, RNF139-AS1	GRCh38.p7	8:124476190	CTTTACCAAGCCTTT[C/G]TGAATTACAAGCCAT	11236
rs79626366	snp	A/C	0.0463947	0.145069	intron-variant	RNF139	GRCh38.p7	8:124484613	AACTTTGGAGATTTG[A/C]AGTTGTAGGAGTGAA	11236
rs80027151	snp	A/C	0	0	intron-variant	RNF139	GRCh38.p7	8:124483053	TATTTAAAAATATAT[A/C]TATTAAAAATATATA	11236
rs111282908	snp	A/G	0	0	intron-variant	RNF139	GRCh38.p7	8:124481917	TTACTTAGGATATTG[A/G]TTTTTAAAATGAGAG	11236
rs111695772	snp	C/T	0.00398564	0.0444627	upstream-variant-2KB, intron-variant, nc-transcript-variant	RNF139, RNF139-AS1	GRCh38.p7	8:124472964	TTTTGGATCTTTTTC[C/T]CCATAATGGCCTCTC	11236
rs111736699	snp	A/G	0.5	0	synonymous-codon	RNF139	GRCh38.p7	8:124486675	GACTGGGTTAAGTGG[A/G]CTAAGACCAGAAGAG	11236
rs111980391	snp	G/T	0.5	0	upstream-variant-2KB, nc-transcript-variant	RNF139, RNF139-AS1	GRCh38.p7	8:124474372	TGGCGTCGGCTTTCA[G/T]ACTCCCGAGGGTGGG	11236
rs112001642	snp	C/T	0.0134861	0.0810011	intron-variant, downstream-variant-500B	TATDN1, RNF139	GRCh38.p7	8:124488760	AGTTCTAAAGCTATA[C/T]AATATTTTTCCACAC	11236
rs112141427	snp	C/T	0.5	0	intron-variant	RNF139	GRCh38.p7	8:124477903	TTCCAAGGAAAAATC[C/T]GAAAAATTTCAGTAC	11236
rs112322932	snp	G/T	0.209997	0.246779	intron-variant	RNF139	GRCh38.p7	8:124478916	TTTTAGTAGAGACAG[G/T]TTTTCTCCATGTTGG	11236
rs112427962	snp	A/T	0.00358779	0.0422022	intron-variant, downstream-variant-500B	TATDN1, RNF139	GRCh38.p7	8:124488895	TATGGACTGTCTTGC[A/T]TATAACTAGAGCTAA	11236
rs112521823	snp	A/T			intron-variant	RNF139	GRCh38.p7	8:124483099	TATATATATTTAAAA[A/T]TATATATATTAAAAA	11236
rs112629245	snp	A/G	0.268995	0.249277	intron-variant	RNF139	GRCh38.p7	8:124482909	CCAGCCTGGGCAACA[A/G]GAGCGAAACTCCATT	11236
rs113027485	snp	A/T	0.0103295	0.0711199	intron-variant	RNF139	GRCh38.p7	8:124478964	TCCCGACCTCAGGTG[A/T]TCTGCCCACATCGTC	11236
rs113267493	snp	A/G	0.0134861	0.0810011	intron-variant	RNF139	GRCh38.p7	8:124477797	CAAGGCAGAAAATGC[A/G]AGCCTAGGAGTTTGT	11236
rs113446645	snp	C/T	0.5	0	intron-variant	RNF139	GRCh38.p7	8:124478574	GATCGCGCCACTGCA[C/T]TCCAGCCTGGGCGAT	11236
rs113915762	snp	C/T	2.50047e-05	0.00353578	missense, upstream-variant-2KB	RNF139, RNF139-AS1	GRCh38.p7	8:124475128	GCGGCCGTGGGGCCC[C/T]CGCAGCAGCAGGTGC	11236
rs113977061	snp	C/G	0.0134861	0.0810011	intron-variant	RNF139	GRCh38.p7	8:124481406	CCAAAAGAGGGTAAG[C/G]GTATGAATAGACTTT	11236
rs114448248	snp	A/G	0.00914312	0.0669923	intron-variant	RNF139	GRCh38.p7	8:124482653	TTTTCAGGGCCGAGC[A/G]CAGTGGCTCACGCCT	11236
rs114484455	snp	A/G	0.0111196	0.0737302	intron-variant	RNF139	GRCh38.p7	8:124484892	GGGAACTTGGAAGAT[A/G]TTTCTAAGTCCGAAG	11236

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