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
rs510858	snp	C/G/T	3.30038e-05	0.00406212	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176918	CGGTGGCCCCCATGT[C/G/T]CTCTGGCCCCACAGG	140432
rs515170	snp	C/T	0.376195	0.215812	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177375	ACAAGAGTGAGTCAC[C/T]GCGCCTGGCCTAGCA	140432
rs626950	snp	C/T	0.375996	0.215928	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177364	TCACCGCGCCTGGCC[C/T]AGCAGAAGCTTTTCT	140432
rs628778	snp	A/G	0.20236	0.245424	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176922	GAAGCCTGTGGGGCC[A/G]GAGGACATGGGGGCC	140432
rs774690	snp	A/T	0.374	0.217081	intron-variant, utr-variant-3-prime	FARP1, RNF113B	GRCh38.p7	13:98176006	CCATGTTCACTGCAG[A/T]ATTATTTGCAAAAGC	140432
rs1853333	snp	A/G	0.203267	0.245593	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179214	cgcatggcagcagac[A/G]agaacagaatgagaa	140432
rs5806050	in-del	-/A	0.290718	0.246662	intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175523	TTTTGAAAAAAAAAA[-/A]TTAATTATAGTACAA	140432
rs5806051	in-del	-/AA	0.499234	0.0195537	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177485	AACTCCATCCTTACT[-/AA]AAATACAAAAATTAC	140432
rs9517208	snp	A/G	0.481473	0.0944461	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178689	ATTCAGCTCACTTGT[A/G]GTGCCCCCAAAACAC	140432
rs9556890	snp	C/T	0.241914	0.249869	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178022	ATTAAAAGACTGTCA[C/T]ATCACACTGCACCTG	140432
rs9556891	snp	A/G	0.0667028	0.170006	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178459	CCTTGGCCTCCTAAA[A/G]TGTTGGTATTACAGG	140432
rs9556892	snp	C/G	0.330016	0.236849	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179097	ctgataaagacacac[C/G]tgagactgggtaatt	140432
rs12868132	snp	C/T	0.00953873	0.0683987	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177761	TCACTTGCTCCTCAG[C/T]TCCCTCAGTGCACAC	140432
rs16955011	snp	C/T	0.13988	0.224441	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176963	TGGACCTGTACACCA[C/T]GTCGAGGCTCTCAGG	140432
rs34253287	snp	C/G	0.0174215	0.091708	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98177012	CCTGTCGCCGTGAGC[C/G]GCCTTCTGCCAGCTG	140432
rs41300600	snp	C/T	0.0105365	0.0718137	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176638	CAGAAGCCAGTCTCC[C/T]TGTAGTCCTTGCAGA	140432
rs56197828	in-del	-/AA	0.499343	0.0278555	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179213	CGCATGGCAGCAGAC[-/AA]GAGAACAGAATGAGA	140432
rs57310501	in-del	-/T			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178213	TTTTTTTTTTTTTTT[-/T]GAGAAAGAGTCTCGC	140432
rs58126526	in-del	-/A	0.498323	0.0289051	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177667	AAAAAAAAAAAAACC[-/A]AAAAAAAAAGGCTTC	140432
rs61968647	snp	A/G	0.00636936	0.0560724	intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175301	TTTGTCTTGGGAGAG[A/G]AATACATTGCCATTT	140432
rs61998176	snp	C/T	0.0259695	0.110952	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176633	AGCCACAGAAGCCAG[C/T]CTCCTTGTAGTCCTT	140432
rs67801656	in-del	-/AA			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179214	GCATGGCAGCAGACG[-/AA]AGAACAGAATGAGAA	140432
rs71111928	in-del	-/AA	0	0	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178190	GCGAGACTCTTTCTC[-/AA]AAAAAAAAAAAAAAA	140432
rs72655114	snp	A/C			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177667	AAAAAAAAAAAAACC[A/C]AAAAAAAAGGCTTCT	140432
rs73561304	snp	A/G	0.0759472	0.179459	intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175689	CAGCTCCCCACTCCC[A/G]CTCTTCCTAACCCCT	140432
rs74575080	snp	A/G	0.0142736	0.0832652	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178066	GGCTTTCATTTTGAA[A/G]TAAAAGTAACACATG	140432
rs74719265	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177652	ACCCTGTCTCAAATT[A/T]AAAAAAAAAAAACCA	140432
rs74851889	snp	A/C			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178021	TATTAAAAGACTGTC[A/C]TATCACACTGCACCT	140432
rs77681464	snp	A/C			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179213	TCGCATGGCAGCAGA[A/C]GAGAACAGAATGAGA	140432
rs78320598	snp	A/C	0.0341408	0.126114	intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175313	GAGGAATACATTGCC[A/C]TTTTAAGGGAGAGGA	140432
rs79275419	snp	G/T	0.0260105	0.111035	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177837	AGGCCATAGCGAACC[G/T]GTGGTGCTCATCCTA	140432
rs79795199	snp	A/C	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177788	ACACTCATTTTTCAA[A/C]AGATTCCTAAAAGGC	140432
rs111427949	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177888	CGTATTTAAAAGCAA[C/T]ACACGCGCAGTGCAG	140432
rs111520418	snp	A/G/T	1.84004e-05	0.00303313	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177101	CCCCGCTGCTGCTGC[A/G/T]CTCTCCGTGCTCGGG	140432
rs113354899	snp	C/T			intron-variant, utr-variant-3-prime	FARP1, RNF113B	GRCh38.p7	13:98175952	ATTTTGTTTGTCCAT[C/T]CATCCATCCATGGAC	140432
rs113453013	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179202	AAAGGCATGTCTCGC[A/G]TGGCAGCAGACGAGA	140432
rs113665583	snp	C/G	0.5	0	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177214	TGGTCGGCCGTCCTT[C/G]CTGGAGAAGGTGGCG	140432
rs113954616	snp	A/G	0.5	0	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176854	CGCTGGCTGCACTTG[A/G]GGATGGTCGGCGTAT	140432
rs114102979	snp	A/G	0.00930212	0.0675613	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176675	GCTGGTAATCCCAGC[A/G]CACAGTGGCGCGCAG	140432
rs114712839	snp	C/G	0.00112795	0.0237214	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176970	GTACACCACGTCGAG[C/G]CTCTCAGGCGCCGCC	140432
rs114739965	snp	A/G	0.00116968	0.0241551	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176780	TCAGGTACCTCAGGT[A/G]GCTGTGGATTCCCCG	140432
rs115032993	snp	A/G/T	0.000708092	0.0188032	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176436	CCTGCACTTGGTGAC[A/G/T]ACTGGGTTTTGGAAG	140432
rs115127901	snp	A/G	0.0341408	0.126114	intron-variant, utr-variant-3-prime	FARP1, RNF113B	GRCh38.p7	13:98176095	TGGGATTGCAGGAAG[A/G]CTGTCATCTCTCTCA	140432
rs115981649	snp	C/T	0.000444675	0.0149044	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176522	CATGGTTTTCGTCCT[C/T]GCAGATACAGTAGCG	140432
rs116650511	snp	C/T	0.000247315	0.0111174	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176839	AGTGCCTCCTGGACC[C/T]GCTGGCTGCACTTGA	140432
rs116765314	snp	C/T	0.00131696	0.025627	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176562	AAGCTCCCGTTCAAT[C/T]TCCCACCCGAGCTTG	140432
rs118043654	snp	C/T	0.0232847	0.105357	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179196	AAGGTGAAAGGCATG[C/T]CTCGCATGGCAGCAG	140432
rs138025858	snp	G/T	0.00014833	0.00861063	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176736	CGCCATCCCCGAGGA[G/T]GAGTTGCCCATGGAC	140432
rs138253916	snp	A/G	0.000331631	0.0128727	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176923	GCCCCCATGTCCTCT[A/G]GCCCCACAGGCTTCG	140432
rs139267423	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178289	CAACCTCTGCCTCCC[A/G]GGTTCAAGCAATTCT	140432
rs140282190	snp	C/T	0.000181224	0.0095173	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176674	GGCTGGTAATCCCAG[C/T]GCACAGTGGCGCGCA	140432
rs140938876	snp	G/T	8.84557e-05	0.00664981	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176986	CTCTCAGGCGCCGCC[G/T]CCTCGCCCCTCCTGT	140432
rs142469809	snp	A/G	4.94173e-05	0.00497053	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176457	GTTTTGGAAGGCCTG[A/G]CGACATATGAAACAC	140432
rs143204738	snp	C/T	0.000461551	0.0151843	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176807	CCCGGTAGATGTGGT[C/T]GTGCTCCCGACCCCG	140432
rs144481331	snp	A/T	0.0023933	0.0345097	intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175558	GTACAAAACATAAAA[A/T]GTACCCTTAACCATT	140432
rs144854034	snp	G/T	0.00132561	0.0257108	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98177134	CGCAGGCCGGGCGCT[G/T]TCTGAGGCCTGCAGC	140432
rs145228466	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178381	CTGTGTTTTTAGTAG[C/T]GACAGGGTTTCACCA	140432
rs145303380	snp	A/G	0.000329658	0.0128343	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176731	TTCCTCGCCATCCCC[A/G]AGGAGGAGTTGCCCA	140432
rs145451325	snp	C/G	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179041	CTTTTTTCTTGGAGA[C/G]CCCCAGATGTTGGTG	140432
rs146499288	snp	C/T	0.00636936	0.0560724	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179130	CAAAAGAAAAAGGCT[C/T]AATGGACTTACATTT	140432
rs146586427	snp	A/C			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177665	TTAAAAAAAAAAAAA[A/C]CAAAAAAAAAGGCTT	140432
rs147264891	snp	C/T	5.18551e-05	0.00509165	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176979	GTCGAGGCTCTCAGG[C/T]GCCGCCTCCTCGCCC	140432
rs147722072	snp	A/G	4.94173e-05	0.00497053	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176415	GCAGCTCTCGCAGAA[A/G]TAATGCCTGCACTTG	140432
rs147920690	snp	C/T			intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98177207	GTCTGCTTGGTCGGC[C/T]GTCCTTCCTGGAGAA	140432
rs148267601	snp	C/G	0.000148377	0.00861198	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176813	AGATGTGGTCGTGCT[C/G]CCGACCCCGCAGTGC	140432
rs148433651	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	FARP1, RNF113B	GRCh38.p7	13:98175812	TAGTTTATTTCACTT[A/G]GCAGTGTCGTCTTCA	140432
rs149265686	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175382	GCGTGGATATTCTTC[A/T]GTCAACTCCTCCCCT	140432
rs149988576	snp	C/T	0.00953873	0.0683987	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178303	CGGGTTCAAGCAATT[C/T]TCCTGCCTCAGCCTC	140432
rs150082041	snp	C/T	0.000230635	0.0107361	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176623	CTGTCCCCGAAGCCA[C/T]AGAAGCCAGTCTCCT	140432
rs151243225	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177967	CCTCAAAGATAACCA[C/G]TGTCAACACTTTTGT	140432
rs151316967	snp	A/G	0.000153988	0.00877328	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176555	CCTCTTCAAGCTCCC[A/G]TTCAATCTCCCACCC	140432
rs181635725	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175368	AAATCCAAACTTCAG[C/T]GTGGATATTCTTCTG	140432
rs181705193	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98179069	GTGTCCATATTAGTC[C/T]GTTTTCACGCTGCTG	140432
rs181779793	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178684	ATGAGATTCAGCTCA[C/T]TTGTAGTGCCCCCAA	140432
rs182388789	snp	A/G	0	0	intron-variant, utr-variant-3-prime	FARP1, RNF113B	GRCh38.p7	13:98176043	ACATACCTCTTTGAG[A/G]TCCGGATTTCAATTC	140432
rs183106529	snp	C/T			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177442	ACCCGAGGTCAGCAG[C/T]TTAAGACCAGCCTGG	140432
rs184244691	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178436	CCTGACCTCAGGTGA[C/T]CCACCCACCTTGGCC	140432
rs184361407	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178831	TCATTTGTCAGTTTT[C/G]TCTTAGGATAGTAAT	140432
rs185073947	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177892	TTTAAAAGCAACACA[C/T]GCGCAGTGCAGAAAA	140432
rs185765267	snp	A/C	0.00119737	0.0244387	intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175645	ACTTTTTCATTTAGC[A/C]AAACTCAAGCTCTGT	140432
rs185956021	snp	A/G	6.59554e-05	0.00574224	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176847	CTGGACCCGCTGGCT[A/G]CACTTGAGGATGGTC	140432
rs187386968	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177463	ACCAGCCTGGCCAAC[A/G]TAGCGAAACTCCATC	140432
rs188748562	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178970	TGGCTGGAATCCATC[A/G]GTATTGTTGGGCTTG	140432
rs189192783	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177313	CTGCACGTGGGGCGT[A/G]GGCCCTCCCAGTTCT	140432
rs189417568	snp	C/T	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178492	TGAGCCACTGCACCC[C/T]GCCTTCAAATATTTT	140432
rs189535288	snp	A/G			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177996	GTGTCTATTCTTTTA[A/G]TATAGCCTTTATTAA	140432
rs190157119	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	FARP1, RNF113B	GRCh38.p7	13:98175855	GTTGTAGCATGTGAT[C/T]CTTAAAAGGATCAGT	140432
rs191799203	snp	A/G			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177874	AGGCGCTTGAAATGC[A/G]TATTTAAAAGCAACA	140432
rs192445596	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177336	CCAGTTCTAAAAAGC[A/G]AAAGCAAGTGAAAGA	140432
rs192788917	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98178354	GTGTGTGCCACCACA[C/G]CCAGCTAACTTCTGT	140432
rs199715561	snp	A/G			intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175523	CTTTTTAGCTTTTTT[A/G]AAAAAAAAAATTAAT	140432
rs199748911	snp	C/T	1.64795e-05	0.00287045	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176700	GCGCAGATGCCCTGG[C/T]GCACGTATGGGGCCC	140432
rs199754785	snp	C/T	0.00199806	0.0315443	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176381	AGCAGCGCGGGGTGG[C/T]CCGGAAGTGCTCCAG	140432
rs199776079	snp	C/G/T	0.000922061	0.0214521	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176473	CGACATATGAAACAC[C/G/T]TGAATGGTATTTCCT	140432
rs199816159	snp	A/G	0.00199792	0.0315431	intron-variant, synonymous-codon	FARP1, RNF113B	GRCh38.p7	13:98176529	TTCGTCCTCGCAGAT[A/G]CAGTAGCGACCCTCT	140432
rs199939990	snp	C/G/T	0.000148431	0.00861367	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176882	TATGGTGCTCCTTCT[C/G/T]GGTGTCCTGCTCGAA	140432
rs200541421	in-del	-/C			intron-variant, upstream-variant-2KB	FARP1, RNF113B	GRCh38.p7	13:98177665	TTAAAAAAAAAAAAA[-/C]CAAAAAAAAAGGCTT	140432
rs200579942	snp	A/G	0.00199808	0.0315444	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176441	ACTTGGTGACGACTG[A/G]GTTTTGGAAGGCCTG	140432
rs200582250	snp	A/T			intron-variant, downstream-variant-500B	FARP1, RNF113B	GRCh38.p7	13:98175534	TTTTGAAAAAAAAAA[A/T]TAATTATAGTACAAA	140432
rs201183546	snp	C/T	0.000247249	0.0111159	intron-variant, missense	FARP1, RNF113B	GRCh38.p7	13:98176345	GGTTAAAGATGCCGC[C/T]GGTTGGCTGGTCACA	140432

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