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
rs11217	snp	C/T	0.0154538	0.0865337	upstream-variant-2KB, intron-variant, utr-variant-5-prime	PAAF1, COA4	GRCh38.p7	11:73876788	GAGGGCCCGAACGCA[C/T]GCTCCTACGCGGCGG	80227
rs635962	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73917824	tgcagtgagccgaga[A/C]catgccactgtgctc	80227
rs825863	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73917618	ggctcacgcctgtaa[C/T]cccagcactttggaa	80227
rs825864	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73917632	accccagcactttgg[A/G]aggccgaggcaggca	80227
rs935985	snp	C/T	0.372181	0.21811	intron-variant	PAAF1	GRCh38.p7	11:73927261	CAAGAATTCACAGTT[C/T]AAAGGAAGCCTGGGA	80227
rs935986	snp	A/T	0.482394	0.0921585	intron-variant	PAAF1	GRCh38.p7	11:73920227	tttaaattaaaaaaa[A/T]atataaaaaatatta	80227
rs935987	snp	C/T	0.0663309	0.169604	intron-variant	PAAF1	GRCh38.p7	11:73920105	aatgttatcacctta[C/T]atttgtcaaaactaa	80227
rs935988	snp	A/C	0.441841	0.160303	intron-variant	PAAF1	GRCh38.p7	11:73919884	TAAGTGAAGCAGTAT[A/C]CTTTCCTAACTGTTT	80227
rs935989	snp	G/T	0.0872718	0.189788	intron-variant	PAAF1	GRCh38.p7	11:73914117	TTTGGATTTACTGAG[G/T]TATCTTTTACATATG	80227
rs1122373	snp	A/G	0.28052	0.24813	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877195	CGAGGGATATGGAGG[A/G]AACAGGGTCCGGAAA	80227
rs1132819	snp	A/G	0	0	intron-variant	PAAF1	GRCh38.p7	11:73880566	GTGGTGGGCCCCTGT[A/G]GTCCCAGCTACTCGG	80227
rs1132820	snp	A/G	0	0	intron-variant	PAAF1	GRCh38.p7	11:73880576	cctgtagtcccagct[A/G]ctcgggagcctgagg	80227
rs1466218	snp	A/C	0.127254	0.217792	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878139	TAGTCTGTATTTTAG[A/C]CCACCTAAATTAAGT	80227
rs1531001	snp	A/G	0.127254	0.217792	intron-variant	PAAF1	GRCh38.p7	11:73895918	tcaagaccaccctgg[A/G]caacatagggggacc	80227
rs1598044	snp	A/G	0.122758	0.215196	intron-variant	PAAF1	GRCh38.p7	11:73920523	ATTATTTTTGAGACA[A/G]AGTCTCGCTTTGTCA	80227
rs1618529	snp	C/T	0.122411	0.214991	intron-variant	PAAF1	GRCh38.p7	11:73921649	GGACAGTGAAAGGAG[C/T]ACGGGCAGCCACCAT	80227
rs1630713	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73883894	gatgaatggataaac[A/C]aaatgtagtatatcc	80227
rs1630767	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73883874	gtagtatatccatac[A/C]acagagtattaccgg	80227
rs1631659	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73883748	ggatcacttgaggcc[A/C]agagttcaagaccag	80227
rs1670539	snp	C/T	0.450609	0.149185	intron-variant	PAAF1	GRCh38.p7	11:73926696	tttgagacagactct[C/T]gctccgtcgctcagg	80227
rs1670543	snp	C/T	0.494057	0.0541878	intron-variant	PAAF1	GRCh38.p7	11:73879265	GACAACAAATGTACT[C/T]AGCTTGGTTTTGGAC	80227
rs1670545	snp	C/G	0.494315	0.0530107	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875067	TATGCTACAGCCACA[C/G]TGAACTCTTTCCATC	80227
rs1670550	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73902934	tcaaactcctgacct[A/T]gtgatcgcctgccgt	80227
rs1670551	snp	A/G	0.498547	0.0269177	intron-variant	PAAF1	GRCh38.p7	11:73904682	AATTTTCCCATATAC[A/G]CATGTATGTATATTG	80227
rs1670552	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73904946	AGACTTGTATCTATT[G/T]GGTTTGATATCTAAA	80227
rs1670553	snp	A/G	0.122758	0.215196	intron-variant	PAAF1	GRCh38.p7	11:73913761	ctaaagaaatatttg[A/G]tgagtaaatgaatAA	80227
rs1670558	snp	G/T	0.496778	0.0400063	intron-variant	PAAF1	GRCh38.p7	11:73899065	TTATAAACTTCCCTT[G/T]TTTCACTCTTCCAAG	80227
rs1670560	snp	A/G	0.0875959	0.190066	intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73889122	CTACGTTTTTCCCAG[A/G]TGTTTTGGCACAGCC	80227
rs1670561	snp	A/G	0.127944	0.218179	intron-variant	PAAF1	GRCh38.p7	11:73890114	AGTACTACTGCAGAA[A/G]AGATAAAAGGTTAGG	80227
rs1792154	snp	G/T	0.498481	0.027514	intron-variant	PAAF1	GRCh38.p7	11:73910360	TGAACAGACAGTAAT[G/T]GTAAGGATAGGACAA	80227
rs1792162	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73883853	tacttcgttcctttt[G/T]gtggcccggtaatac	80227
rs1792169	snp	A/C	0	0	intron-variant	PAAF1	GRCh38.p7	11:73925667	CAAATAGAGAAAAAC[A/C]AAAGGGGAATATTTA	80227
rs1792170	snp	G/T	0.50375	0.0473547	intron-variant	PAAF1	GRCh38.p7	11:73902812	AGCAATTCTCCTGCC[G/T]CAGCCTCCCCAGTAA	80227
rs1792171	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73904696	CGCATGTATGTATAT[G/T]GCTCCCTAGCAACAT	80227
rs1792172	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73904785	GGGGAATATGAAATT[G/T]GCTTTATTTCTTACA	80227
rs1792173	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73904951	TGTATCTATTGGGTT[G/T]GATATCTAAAGCCTT	80227
rs1792188	snp	G/T	0	0	intron-variant	PAAF1	GRCh38.p7	11:73920015	ctttccttaacatcc[G/T]ggatccaatccagaa	80227
rs1792197	snp	A/G	0.127254	0.217792	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73874815	GGATGATGAAACCCC[A/G]TCTCTACTAAAAATA	80227
rs1792198	snp	A/G	0.49655	0.04139	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875505	CCACAGTGGAGGGAT[A/G]CCTAATCCAGACAAG	80227
rs1792199	snp	A/G	0.496714	0.0404017	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877525	CTGTGTCCAGGCCCC[A/G]TACTGGATGCTTGGT	80227
rs1792201	snp	G/T	0	0	intron-variant	PAAF1	GRCh38.p7	11:73907225	AATCGATAGGCATTT[G/T]GGACATTATAACACT	80227
rs1792202	snp	A/G	0.123105	0.215401	intron-variant	PAAF1	GRCh38.p7	11:73907399	CACACTGCAGACAGG[A/G]GAGGTGGAAGTTCAG	80227
rs1792203	snp	A/G	0.408359	0.193449	intron-variant	PAAF1	GRCh38.p7	11:73908401	tgtatatatatatgt[A/G]tatatatatgtgtgt	80227
rs2010583	snp	C/G	0.280256	0.248162	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876952	CCCACCTCTGTCCTC[C/G]CCGCACGCTTCTCGG	80227
rs2060964	snp	C/T	0	0	intron-variant	PAAF1	GRCh38.p7	11:73889645	AAGAAATGAAGTCTT[C/T]TGAGAGCAAATCCAA	80227
rs2067912	snp	C/G	0.156407	0.23182	missense, intron-variant, nc-transcript-variant	PAAF1	GRCh38.p7	11:73900304	TGTTTGATGTGAATT[C/G]TTGCAGGTTTTTCCC	80227
rs2067913	snp	C/G	0.343219	0.23197	intron-variant	PAAF1	GRCh38.p7	11:73900433	GAGGTATGAAGTGTG[C/G]TTTCTCCAAAAGGCT	80227
rs2444601	snp	A/G	0.491987	0.0627894	intron-variant	PAAF1	GRCh38.p7	11:73899971	CACAGCCATCTCTAG[A/G]TCTAGTTAAAGAGCT	80227
rs2511260	snp	C/T			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887139	ttataaattacccag[C/T]ctcaggtattccttt	80227
rs2511274	snp	C/T	0	0	intron-variant	PAAF1	GRCh38.p7	11:73907082	TGTGTATTTTTTCTC[C/T]TTTTTTTTTTCCATT	80227
rs2515095	snp	A/G	0.123105	0.215401	intron-variant	PAAF1	GRCh38.p7	11:73907142	CCTAGCCTCAGGAAT[A/G]CACAGCATAAAAAAA	80227
rs2886812	snp	G/T	0.127254	0.217792	intron-variant	PAAF1	GRCh38.p7	11:73894114	GGCCTTTATACATCA[G/T]TTTTTATTATTTTCT	80227
rs3018335	snp	C/T	0.494272	0.053207	intron-variant	PAAF1	GRCh38.p7	11:73897966	CTGGCGGATCACTCA[C/T]GGTTAGGAGCTGCAG	80227
rs3019137	snp	A/T	0.127254	0.217792	intron-variant	PAAF1	GRCh38.p7	11:73894592	acgtgcacaatgtgc[A/T]ggttagttacatatg	80227
rs3076363	in-del	-/AGAG	0.123452	0.215605	intron-variant	PAAF1	GRCh38.p7	11:73901087	TGTGTGCTGGGAAAT[-/AGAG]AGAGAGAGTGAGAGA	80227
rs3211440	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73921405	AAATTTCTAACATTC[A/C]AAAAAAAAAAAGTAC	80227
rs3741138	snp	C/G	0.194819	0.243834	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909492	AGGACTCCCAAGCAG[C/G]CTGAGCGCCCACAAT	80227
rs3741139	snp	C/T	0.258288	0.249863	intron-variant	PAAF1	GRCh38.p7	11:73900475	TTTCTACCTTTTCAG[C/T]GATTCATTTCTGGGG	80227
rs3758930	snp	A/C	0.100588	0.200439	intron-variant	PAAF1	GRCh38.p7	11:73879119	TTCAACTGGGACTTT[A/C]Ttgatgataatttct	80227
rs3758932	snp	A/G	0.171704	0.237423	intron-variant	PAAF1	GRCh38.p7	11:73879608	CAGTGGCTCACACCT[A/G]TAATCCTAGCACTTT	80227
rs3758933	snp	A/G	0.171704	0.237423	intron-variant	PAAF1	GRCh38.p7	11:73879689	TGGGCAACAAAGTGA[A/G]ACCCCCTCCCCATCT	80227
rs3926010	snp	C/T	0.388587	0.208071	intron-variant	PAAF1	GRCh38.p7	11:73926350	agcactttgggaggc[C/T]gaggcaggcctcagt	80227
rs4362170	snp	G/T	0.494272	0.053207	intron-variant	PAAF1	GRCh38.p7	11:73894364	AACAAAATAGGCTGG[G/T]TGTAGTGGCTCACAC	80227
rs4944035	snp	A/G	0.0126979	0.078662	intron-variant	PAAF1	GRCh38.p7	11:73922602	gcgggcggatcacga[A/G]gtcaggagatcgaga	80227
rs5792635	in-del	-/T	0.49703	0.0384237	intron-variant	PAAF1	GRCh38.p7	11:73896307	TTTCTTTTTTATTTA[-/T]TTTTTTTTTTATTGA	80227
rs5792636	in-del	-/A			intron-variant	PAAF1	GRCh38.p7	11:73900982	GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	80227
rs6592541	snp	C/T	0.100231	0.200173	intron-variant	PAAF1	GRCh38.p7	11:73909331	GTCATTTATGCAGCT[C/T]CATCTTCTCTGCCCT	80227
rs7102066	snp	A/T	0	0	intron-variant	PAAF1	GRCh38.p7	11:73902443	AGTGCAAGCTTCACC[A/T]CCGATCTGGCCATCC	80227
rs7105293	snp	A/G	0.496746	0.040204	intron-variant	PAAF1	GRCh38.p7	11:73881150	TAATAAACTGTAACC[A/G]AAAGGCACAGTTTCT	80227
rs7107228	snp	C/T	0.00279162	0.0372561	intron-variant	PAAF1	GRCh38.p7	11:73913166	acaggcgtgagccac[C/T]gcacctggcctgact	80227
rs7114340	snp	C/T	0.100231	0.200173	intron-variant	PAAF1	GRCh38.p7	11:73927142	AACAATTTTTGTAAG[C/T]ACATAATTATGGATG	80227
rs7115579	snp	A/G	0.0599851	0.162463	intron-variant	PAAF1	GRCh38.p7	11:73915565	gtgagccaagattgc[A/G]ccactgtactccagc	80227
rs7119270	snp	A/G	0.0228947	0.104514	intron-variant, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73888502	TGACTGCTGCAGTTA[A/G]TATGCTCTGGTGAGA	80227
rs7119602	snp	C/G	0.27278	0.24896	intron-variant, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73888755	GTATTATAGGTATCA[C/G]AAGATCTAAGTCTTA	80227
rs7122397	snp	C/T	0.100231	0.200173	intron-variant	PAAF1	GRCh38.p7	11:73904717	CTAGCAACATTAAAA[C/T]AGCTTAATATGATAG	80227
rs7123227	snp	A/G	0.121022	0.21416	intron-variant	PAAF1	GRCh38.p7	11:73922901	AGTGAGGAGATTTAA[A/G]TTGCCAGATGAAACA	80227
rs7123871	snp	C/T	0.00398564	0.0444627	intron-variant	PAAF1	GRCh38.p7	11:73922644	aacatggtgaaaccc[C/T]gtctctactaaaaat	80227
rs7926863	snp	C/T	0.100231	0.200173	intron-variant	PAAF1	GRCh38.p7	11:73906986	CATAGGGTTGCACTA[C/T]CTCTCTACTCCATAC	80227
rs7927396	snp	A/G	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73900839	tacaaaaaattagcc[A/G]ggcgtagtggcgggc	80227
rs7934784	snp	C/T	0.4941	0.0539917	intron-variant	PAAF1	GRCh38.p7	11:73892752	gcaagctccacctcc[C/T]gggttcacaccattc	80227
rs7937252	snp	A/G	0.121022	0.21416	intron-variant	PAAF1	GRCh38.p7	11:73911877	ggcctcaagtgatcc[A/G]ccctcctaagcctcc	80227
rs7940614	snp	A/G	0.0707826	0.174302	intron-variant	PAAF1	GRCh38.p7	11:73912298	ttcgatgtctaataa[A/G]taagttgaacttacc	80227
rs7942963	snp	A/G	0.166506	0.235645	intron-variant	PAAF1	GRCh38.p7	11:73904554	AGTATCAGCACTTGC[A/G]CCATTATTTTCCAAG	80227
rs7944702	snp	A/G	0.100231	0.200173	intron-variant	PAAF1	GRCh38.p7	11:73892729	cagtggtgcagtctc[A/G]gctcactgcaagctc	80227
rs9651759	snp	A/G	0.127254	0.217792	intron-variant	PAAF1	GRCh38.p7	11:73891905	GGAATAATTTTCAAA[A/G]GTCTTTGTGATATAA	80227
rs9705041	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73894301	tgagcccaggagttt[A/G]agaccagcctaggca	80227
rs9705042	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73894303	agcccaggagtttga[A/G]accagcctaggcaac	80227
rs9734960	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73880688	caagactctgtctcg[A/G]aaaaaaaaaaaaaaa	80227
rs10128615	snp	C/T	0.372592	0.217879	intron-variant	PAAF1	GRCh38.p7	11:73926115	TTTCTTTCTTTCTTT[C/T]TTTTTTTTGAGATGG	80227
rs10543174	in-del	-/TA	0.103438	0.202533	intron-variant	PAAF1	GRCh38.p7	11:73908286	ATATGTGTATATATG[-/TA]TATATATGTGTGTAT	80227
rs10590637	in-del	-/TG	0.100231	0.200173	intron-variant	PAAF1	GRCh38.p7	11:73892695	GATGGAGTCTCGCTC[-/TG]TTGCCCAGGCTGGAG	80227
rs10656357	in-del	-/TAATT	0.100231	0.200173	intron-variant	PAAF1	GRCh38.p7	11:73904742	GATAGAGAAACTAAA[-/TAATT]TAAATACACTTGTTA	80227
rs10793067	snp	A/G	0.498547	0.0269177	intron-variant	PAAF1	GRCh38.p7	11:73918424	GATCACTATTATAAA[A/G]TCACACTTACATATA	80227
rs10898950	snp	A/G	0.455383	0.142541	intron-variant	PAAF1	GRCh38.p7	11:73889843	GCAAAAACTCATTTA[A/G]TGAAAGGCCTGCAGG	80227
rs10898952	snp	C/T	0	0	intron-variant	PAAF1	GRCh38.p7	11:73918251	AAAACAGGAGCTGCT[C/T]TGACCTTACCTGCCA	80227
rs11235937	snp	C/T	0.298398	0.245271	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875484	TACAGATAGCAAAGA[C/T]TGGGACCACAGTGGA	80227
rs11235938	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73879543	TATCTTTCATTTCAA[A/G]TGCTGCTGATATATT	80227
rs11235939	snp	A/G	0.209997	0.246779	intron-variant	PAAF1	GRCh38.p7	11:73892174	CAGAAAAATACAAAA[A/G]TTAGCCAGACATGGT	80227
rs11235940	snp	C/T	0.190205	0.242744	intron-variant	PAAF1	GRCh38.p7	11:73893315	CTCTGTAAAACATAC[C/T]GTTAGGTTGAAAGTT	80227
rs11235941	snp	A/G	0.190205	0.242744	intron-variant	PAAF1	GRCh38.p7	11:73894018	ctgttgcccaggctg[A/G]tctcaaactcctgac	80227

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