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
rs8462	snp	A/G	0.3512	0.228601	utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121424268	TCACTATACAAAACA[A/G]TGTAAACTGATTACA	80196
rs750008	snp	C/G	0.0486741	0.148216	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419701	TTTGTGTTTTCTAAA[C/G]TGTTCTGATTGAGAA	80196
rs889970	snp	C/T	0.47852	0.101384	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418414	TGTCCAAGGACCTCA[C/T]TGGGACAATATTATT	80196
rs1110337	snp	A/G	0	0	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420730	AAATGGGAACTGGTA[A/G]AGAAAGTAAACCGGT	80196
rs1177625	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408270	tatttttagtagaga[C/G/T]ggggtttcaccatgt	80196
rs1177626	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408190	gcctcccaaagtgtt[A/G]ggattacaggcgtga	80196
rs1177634	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410070	acctcccaggttcaa[C/G]cgattctcctgcctc	80196
rs1182952	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408229	ggtctcgaactcctg[A/G]cctcaggtgatctgc	80196
rs1305816	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410142	tttgagacggagttt[C/T]gctcttgtcacccag	80196
rs1305817	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410125	ctcttgttgcccagg[C/T]tggagtgcagtggcg	80196
rs1612971	snp	A/C/G	0	0	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410916	CCAAGCCAACCTCCA[A/C/G]AGTGTCCCAGGCAAA	80196
rs1706458	snp	A/G	0.200182	0.244986	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413641	gcagtgagcccagat[A/G]gcaccactgcactcc	80196
rs1706459	snp	A/G	0.390277	0.206936	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413428	caaaactccgtctca[A/G]aaaaaaaaaaaaGGA	80196
rs2293462	snp	C/T	0.350982	0.228698	intron-variant	RNF34	GRCh38.p7	12:121401051	ACTTTCAGACCTAGA[C/T]GGTTTCGTTAATCTC	80196
rs2293463	snp	A/G	0.350764	0.228794	intron-variant	RNF34	GRCh38.p7	12:121401153	TCAAAGATTTACTAT[A/G]GAAGATTGAAAAAGA	80196
rs2552078	snp	C/T					GRCh38.p7	12:121415017	cgtccgcctcccggg[C/T]tcaagcgattctcct	80196
rs2668257	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415000	gctggggaggctgag[A/G]caggagaatcgcttg	80196
rs2668258	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415038	gaggcggacgttgca[G/T]tgagccgagatcacg	80196
rs2695150	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414937	agctaattttttgta[C/G/T]ttttggtagacacag	80196
rs3080027	in-del	-/TA/TAG	0	0	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419578	GTGCCTGGCAATCAG[-/TA/TAG]GGTGGAATATTTGAA	80196
rs3751132	snp	A/C	0.00119737	0.0244387	utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423998	GAGCCACTGCTCAGC[A/C]TGTTCCATGTCGGCC	80196
rs3751133	snp	A/G	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422743	TAAGAAAGACGATGA[A/G]TAAGTTAAAAAAAAG	80196
rs3751134	snp	A/C	0.3512	0.228601	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420409	CCTGTACTAATCTAG[A/C]GAATGTCCACAGGGC	80196
rs3751135	snp	A/T	0.3512	0.228601	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420405	TACTAATCTAGCGAA[A/T]GTCCACAGGGCACTG	80196
rs3763973	snp	C/T	0.350764	0.228794	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399338	TATTTTTGACAAGGT[C/T]TTGCTCTTGCCCAGG	80196
rs3842646	in-del	-/T	0.351418	0.228505	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422916	GAGCCTTAGTTCCCC[-/T]CTTAGGAAAGTTAGG	80196
rs4081775	snp	C/T	0.416218	0.186739	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409776	TTTTAGTCCTGTACC[C/T]TCGTAGCTGCTGTCA	80196
rs4640009	snp	C/T	0.3512	0.228601	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422116	ATGTACAGTGCACAA[C/T]GATAATGCCATTCCC	80196
rs7132130	snp	A/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410581	TGGGAAAAAAAAAAA[A/T]ACTTCAAATATACTA	80196
rs7296507	snp	A/G	0.478603	0.101197	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409332	ACCAAAGTGGGATGC[A/G]AAATACTACATATCC	80196
rs7301132	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410410	ggtgtggtggtgggt[G/T]cctgtaatcccggct	80196
rs7311543	snp	A/C	0.350982	0.228698	intron-variant	RNF34	GRCh38.p7	12:121400757	ACGTCGGGGCCGCGA[A/C]CTAGAGAAGGCTGGA	80196
rs7311592	snp	A/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421684	ttatttttttctttt[A/T]aattgtaaaaaaaat	80196
rs7311596	snp	A/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421690	ttttctttttaattg[A/T]aaaaaaaatatatat	80196
rs7311769	snp	C/T	0.029116	0.117091	intron-variant	RNF34	GRCh38.p7	12:121400818	CAAGGAATTTGGCAG[C/T]TTGAGTTCTCCAAGG	80196
rs7961800	snp	A/G	0.00597247	0.0543191	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422024	GAGCTTTCAGAGGTC[A/G]TAGGCTGCTGGCTGG	80196
rs10744761	snp	C/T	0.492727	0.0598633	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398223	TAAAAATACAAAAAA[C/T]TAGCCGGGCGCGGTG	80196
rs10744762	snp	A/C	0.492435	0.0610346	intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121401898	GACATCAGCCTGTGC[A/C]AGATGACAGTTATAA	80196
rs10774594	snp	A/G	0.416218	0.186739	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404917	CTTGAGGCCATTTGA[A/G]AATCCTGGCACTGTG	80196
rs10849875	snp	A/G	0.415891	0.18703	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398176	CAGGAGATCGAGACC[A/G]TCCTGGCTAACACGG	80196
rs10849876	snp	A/G	0.479014	0.100263	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398302	gcgtgaacccaggag[A/G]cggagcttgcagtga	80196
rs10849877	snp	A/G	0.416218	0.186739	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404465	GGTGGCACCATCTCA[A/G]CTTACTGCAGTCTCC	80196
rs10849878	snp	A/G	0.417196	0.185864	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406489	ATGGCGTTTCACCAC[A/G]TTGCCCACGCTGGTC	80196
rs10849879	snp	A/T	0.416218	0.186739	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411512	TTGTATTCTTCCCTA[A/T]TTCATTGTAAAACTA	80196
rs10849880	snp	A/C	0.416708	0.186302	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422041	AGGCTGCTGGCTGGG[A/C]AATGGTTTTCTGGCA	80196
rs11065555	snp	A/T	0.444444	0.157135	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398385	TCAAAAAAAAAAAAA[A/T]TTTTTTTTTTAAGAA	80196
rs11065556	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398614	TTAACTCTGGAGGTA[A/G]ACCTGCCAGGCCTTT	80196
rs11065557	snp	A/C/G	0	0	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398664	GGCTTTGTACCCCAA[A/C/G]AACATTTTTATTGAG	80196
rs11065558	snp	A/G	0.00649344	0.0566088	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398813	GACTATTATGGATAA[A/G]AAGTGACATTATCTG	80196
rs11065559	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404658	AAAGTGCTGGGATTA[A/G]AGGTGTGAGCTACTG	80196
rs11065560	snp	A/G	0	0	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407760	AAGAACATGAACTTA[A/G]GTCTCTAAAGCTTTT	80196
rs11065561	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412169	TGGGTTCAAGCGATT[C/T]TCCTGCCTCAGCCTC	80196
rs11065562	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413101	TGCGATCTAGGCTCA[C/G]TGCAACCTCCGCCTC	80196
rs11065563	snp	C/T	0.416218	0.186739	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413466	GCCCAAGCTGGAGTG[C/T]GGTGGCACAATCTTG	80196
rs11065564	snp	A/G	0.3512	0.228601	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414327	GGCAAAAGCCTATTC[A/G]TTCTAAACACTATAG	80196
rs11065565	snp	C/T	0.445196	0.1562	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415361	CATAGTGGCTCACAC[C/T]TGTAATCTGAGCACT	80196
rs11065566	snp	C/T	0.478354	0.101757	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415570	GCAGTGAGCCGAGAT[C/T]GCGCCACTGTACTCC	80196
rs11065567	snp	C/T	0.01233	0.0775433	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421247	TGAGGTTAAGAACTT[C/T]TGAACTAggctgggc	80196
rs11398833	in-del	-/A/C			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421372	GAGATCCCATCTCTA[-/A/C]AAAAAAAAAAAAAAA	80196
rs11446752	in-del	-/A			intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121424725	AAAAAAAAAAAAAAA[-/A]GAAAAAAAAGAAAAA	80196
rs11545004	snp	A/G			intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417600	CACTTATTACAAGAG[A/G]CAGCATTTCAGCGCC	80196
rs11545005	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121424187	TGTTCAGGTATAGCT[C/T]TTTATAGCAAGGGCT	80196
rs11610134	snp	A/G	0.00934559	0.067716	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417375	CATGAAAATACCTCT[A/G]GAAATAGTCTGGTGC	80196
rs11612856	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412706	TAAATTAACTCTTAG[G/T]GAATCTAGATGTTCA	80196
rs11615530	snp	A/G	0.00159617	0.0282053	intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121401872	TCAGAAGCAAAATAT[A/G]GACCTGAATAGACAT	80196
rs11829166	snp	G/T	0.350982	0.228698	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404784	TTAAAAGTTTAGGGT[G/T]GAAAATTTGTGGTAA	80196
rs11830100	snp	A/G	0.00478085	0.0486577	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410150	caagagcgaaactcc[A/G]tctcaaaaaaaaaga	80196
rs11830307	snp	A/T	0.34659	0.230587	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398384	CTCAAAAAAAAAAAA[A/T]TTTTTTTTTTTAAGA	80196
rs11831204	snp	C/T	0.350764	0.228794	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408206	AACACTTTGGGAGGC[C/T]GAGGCAGGCAGATCA	80196
rs11831315	snp	C/T	0.245452	0.249959	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402831	TGTATCTATAGCACA[C/T]GTTATTGTAATAATC	80196
rs11833355	snp	A/G	0.3512	0.228601	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408127	CCTGGGCAGCATATC[A/G]AGACCCCGTCTCTAA	80196
rs11837988	snp	C/T	0.350764	0.228794	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398486	TCCACATCCTCACCA[C/T]CTATTTTCTTTCTTT	80196
rs12099579	snp	A/G	0.184838	0.241358	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412187	CTGCCTCAGCCTCCC[A/G]ACTAGCTGGGACTAC	80196
rs12314670	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404415	tttttttttttttga[A/G]atggagtctctcttt	80196
rs12321719	snp	A/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404417	tttttttttttgaga[A/T]ggagtctctctttgt	80196
rs12368549	snp	A/T			intron-variant	RNF34	GRCh38.p7	12:121401352	CAGAAGGCTATAGGT[A/T]TCaaaaaaaaaaaaa	80196
rs12369641	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421285	ctcacaactgtaatt[C/T]taggactttgggagg	80196
rs12371831	snp	C/T			intron-variant	RNF34	GRCh38.p7	12:121401344	TTACAAGGCAGAAGG[C/T]TATAGGTATCaaaaa	80196
rs12810275	snp	C/G			upstream-variant-2KB	RNF34	GRCh38.p7	12:121399544	AGAGCCCTTGGTTTT[C/G]TAAGTGTTTTCAATA	80196
rs12811672	snp	G/T	0	0	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399520	TTTTCAAAGAGCCCT[G/T]GGGATTTGAGAGCCC	80196
rs12812023	snp	A/T	0	0	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408913	AAAAGTTACAGGCCA[A/T]TCTGTGGTAAAAAGG	80196
rs12813638	snp	G/T	0	0	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408914	AAAGTTACAGGCCAA[G/T]CTGTGGTAAAAAGGA	80196
rs12815395	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412786	ctggagtgcagtggc[A/G]tgatctcggctcact	80196
rs28398328	snp	A/G			intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121424737	AAAAGAAAAAAAAGA[A/G]AAAAACAATGCCACA	80196
rs28493526	snp	A/G			intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121424726	AAAAAAAAAAAAAAA[A/G]AAAAAAAAGAAAAAA	80196
rs28557279	snp	A/C	0.255521	0.249939	utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423621	CCCAAACTTGACCCC[A/C]AACATTTCAATGCAC	80196
rs34194877	snp	A/G	0.0704125	0.17392	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403128	GAGGCCGGGCGCGGT[A/G]GCTCACGCCTGTAGT	80196
rs34621569	in-del	-/G			upstream-variant-2KB	RNF34	GRCh38.p7	12:121398881	ATTATTTCAGTCTAA[-/G]GGAAGTGGCCTGCCA	80196
rs34735211	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422155	GTACTTTGCGGCGTA[A/G/T]GATATAACATGGTTG	80196
rs34812514	snp	C/G			missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420664	ATGAGCGTGCGCCAG[C/G]TGAAGGAAATTCTGG	80196
rs34892758	in-del	-/G			intron-variant	RNF34	GRCh38.p7	12:121400617	ACTAACCCAAGTGTT[-/G]GGGGACATCGTGGGA	80196
rs35270866	in-del	-/AGT	0.492484	0.0608394	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419576	TGGTGCCTGGCAATC[-/AGT]AGGGTGGAATATTTG	80196
rs35375423	in-del	-/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416859	AGACCCATCATATTG[-/G]GTAGGCCTCCTTGCT	80196
rs35628523	in-del	-/C			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407799	GTGCAGAAGAGGGAT[-/C]CCTTGTTGGTTATGA	80196
rs35917782	in-del	-/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413575	GCCACCATGCCCAGC[-/T]TTTTTTTTTTTTTTT	80196
rs35925457	in-del	-/A/ACAA			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421371	AGAGATCCCATCTCT[-/A/ACAA]AAAAAAAAAAAAAAA	80196
rs36077205	in-del	-/G			intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121424549	TAGCTTGGACAACAT[-/G]GGCGAAACCCTGTCT	80196
rs41367546	snp	A/C	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417432	ATTAAATTTTAGTAG[A/C]AGGCRGAAAGAAAAC	80196
rs41422244	snp	C/T	0.00161617	0.0283809	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402846	YGTTATTGTAATAAT[C/T]GATCAGTTTGGCCAA	80196
rs41468645	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417437	ATTTTAGTAGMAGGC[A/G]GAAAGAAAACTCATG	80196

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