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
rs735	snp	A/G	0.0861826	0.188849	intron-variant	CFAP44	GRCh38.p7	3:113335461	CTTCTGGAAATCTAC[A/G]TAGCGCCTTAACATT	55779
rs4251	snp	C/T	0.003992	0.0444979	intron-variant	CFAP44	GRCh38.p7	3:113335498	GAGTATTAATCTGTA[C/T]ATGTGTAATGTGAAC	55779
rs712530	snp	C/T	0.469346	0.119947	intron-variant	CFAP44	GRCh38.p7	3:113297109	GTAAAACTGACTCAA[C/T]GTTCCCAACTGGATT	55779
rs763804	snp	G/T	0	0	intron-variant	CFAP44	GRCh38.p7	3:113353894	tctgttcctttcagg[G/T]gtttcttttcccagc	55779
rs763805	snp	G/T	0.343254	0.231956	intron-variant	CFAP44	GRCh38.p7	3:113353779	CTCTCTCTGACTCTG[G/T]TTCTCTCTCTCTGAC	55779
rs775214	snp	C/T	0.427423	0.176128	intron-variant	CFAP44	GRCh38.p7	3:113292103	GAAATCTTCTGTTTC[C/T]TCATCGGAGTTATTT	55779
rs775215	snp	C/G	0.399611	0.200291	intron-variant, downstream-variant-500B	CFAP44	GRCh38.p7	3:113293483	GGCCATACATGTAAA[C/G]ATATACTGTGTAAAG	55779
rs775216	snp	A/G	0.00993419	0.0697739	intron-variant, downstream-variant-500B	CFAP44	GRCh38.p7	3:113293927	TTCTGAAGCAGTACA[A/G]CTGGGTTGGGGCCTT	55779
rs775217	snp	A/G	0.427119	0.176434	intron-variant, utr-variant-3-prime, nc-transcript-variant	CFAP44	GRCh38.p7	3:113294127	TAACATAGAGTTTGG[A/G]ATATGCTATACATGT	55779
rs775218	snp	A/T	0.113685	0.209567	intron-variant, utr-variant-3-prime, nc-transcript-variant	CFAP44	GRCh38.p7	3:113294344	CAAGTCAAATGAAAT[A/T]TGCAGATATTGGAAA	55779
rs775231	snp	A/C	0.321053	0.23969	intron-variant	CFAP44	GRCh38.p7	3:113308367	TGAGTTAGTCACTAG[A/C]AAAATAACTCAATAT	55779
rs775232	snp	C/G	0.480144	0.097642	intron-variant	CFAP44	GRCh38.p7	3:113313864	ctttttcttcccagt[C/G]ttgagtatgtcttta	55779
rs775233	snp	C/T	0.480223	0.0974544	intron-variant	CFAP44	GRCh38.p7	3:113316634	agcactttgagagac[C/T]gaggtgggtggatca	55779
rs775234	snp	A/C	0.0376037	0.131863	intron-variant	CFAP44	GRCh38.p7	3:113318704	cacatacagagagaa[A/C]cccatcaggctagca	55779
rs799828	snp	A/G	0.031825	0.122064	intron-variant	CFAP44	GRCh38.p7	3:113310262	cccctctcccctcag[A/G]ggtggtatcagaaga	55779
rs799829	snp	A/G	0.0376037	0.131863	intron-variant	CFAP44	GRCh38.p7	3:113315663	aacgttttgacttat[A/G]atttttcagctttat	55779
rs808949	snp	C/G	0.426813	0.17674	intron-variant, downstream-variant-500B	CFAP44	GRCh38.p7	3:113296589	CGAGACAAGGCCTAA[C/G]ATCCTGGGGCAGCCA	55779
rs808950	snp	A/C	0.385156	0.210316	intron-variant, downstream-variant-500B	CFAP44	GRCh38.p7	3:113296706	TTCAACCAAAGATCA[A/C]CCCCCTTCTCTTCCT	55779
rs810209	snp	A/G	0.426966	0.176587	intron-variant, downstream-variant-500B, splice-donor-variant	CFAP44	GRCh38.p7	3:113293950	GGGGCCTTAGCACCT[A/G]CATTTTAAACAAGTT	55779
rs812314	snp	G/T	0.0930568	0.194599	utr-variant-3-prime, nc-transcript-variant	CFAP44	GRCh38.p7	3:113290341	CACCTCTAAGAATAT[G/T]CTGATGTACAAAGAA	55779
rs1055748	snp	C/G	0.486464	0.0811471	utr-variant-3-prime, nc-transcript-variant	CFAP44	GRCh38.p7	3:113290342	TTTCTTTGTACATCA[C/G]CATATTCTTAGAGGT	55779
rs1082588	snp	C/T	0.427119	0.176434	intron-variant	CFAP44	GRCh38.p7	3:113295446	GATTGCATATATTAT[C/T]GCCAACATTCCCTTA	55779
rs1082589	snp	C/T	0.46885	0.12085	intron-variant, downstream-variant-500B	CFAP44	GRCh38.p7	3:113296346	TTCATTTTCTCATTG[C/T]GGTTTTAATTTGCAT	55779
rs1082590	snp	A/G	0.0329836	0.124112	intron-variant	CFAP44	GRCh38.p7	3:113316360	tcatcaataatctaa[A/G]ctcccacaacaaaac	55779
rs1353903	snp	A/G	0.474813	0.109357	intron-variant	CFAP44	GRCh38.p7	3:113309487	tattgtttttaataa[A/G]tgtcaggaatgattt	55779
rs1386336	snp	C/T	0.25801	0.249872	intron-variant, utr-variant-5-prime	CFAP44, CFAP44-AS1	GRCh38.p7	3:113425306	TAGTACTTATCACCA[C/T]GTGGCCTAAACCACC	55779
rs1392284	snp	A/G	0.475081	0.108804	intron-variant	CFAP44	GRCh38.p7	3:113382563	taagtgggagaaaca[A/G]gaacatatttaaata	55779
rs1392285	snp	C/T	0	0	intron-variant	CFAP44	GRCh38.p7	3:113353870	tgcataagaaggagt[C/T]tatctgaggctggga	55779
rs1392286	snp	C/T	0	0	intron-variant	CFAP44	GRCh38.p7	3:113353989	gggacataggatatt[C/T]tgctcagaagagtgt	55779
rs1392287	snp	C/T	0	0	intron-variant	CFAP44	GRCh38.p7	3:113354008	tcagaagagtgttgt[C/T]ttagtagctggaaaa	55779
rs1463640	snp	C/T	0.475081	0.108804	intron-variant	CFAP44	GRCh38.p7	3:113373350	TGTCTATGCTTTTGT[C/T]CATCATGGATATTGT	55779
rs1463641	snp	G/T	0.170084	0.236883	intron-variant	CFAP44	GRCh38.p7	3:113395933	ATCACAAAAAAGCAT[G/T]TAATAACATAACGCT	55779
rs1463642	snp	A/G	0.170084	0.236883	intron-variant	CFAP44	GRCh38.p7	3:113396032	ATTTTCCCCATTAGA[A/G]CATTTGGAAAACCAT	55779
rs1486895	snp	A/C	0.00914312	0.0669923	intron-variant	CFAP44	GRCh38.p7	3:113378780	TTCTTCCTTATGAGC[A/C]AAGTTCTGATTTTGT	55779
rs1486896	snp	C/T	0.031825	0.122064	intron-variant, upstream-variant-2KB	CFAP44, CFAP44-AS1, MIR8076	GRCh38.p7	3:113432699	GCAGTATACTAAAAA[C/T]AGTAAGCATGGACTT	55779
rs1553220	snp	A/T	0.122981	0.215328	intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	CFAP44, BOC	GRCh38.p7	3:113286908	TTCTTCTTTTTTTTT[A/T]TAAAAAAAAAACAAT	55779
rs1906141	snp	C/T	0.158962	0.232835	upstream-variant-2KB, downstream-variant-500B, intron-variant	CFAP44, SPICE1	GRCh38.p7	3:113442672	TTTATATACAATAAA[C/T]GACATCCATTTAAAG	55779
rs1906142	snp	A/G	0.484138	0.0876334	intron-variant, upstream-variant-2KB	CFAP44	GRCh38.p7	3:113435376	gttttcttccccttc[A/G]ctctgcacttctcct	55779
rs1979553	snp	C/G	0.0260105	0.111035	intron-variant	CFAP44	GRCh38.p7	3:113362018	CTGGTGGCAGTTATC[C/G]TTGAGGAACCTTCAG	55779
rs1979554	snp	A/G	0.484491	0.0866827	intron-variant	CFAP44	GRCh38.p7	3:113362004	CCTTGAGGAACCTTC[A/G]GTGTGTGGTGGGAAG	55779
rs2018912	snp	A/G	0.197703	0.244469	intron-variant, downstream-variant-500B	CFAP44	GRCh38.p7	3:113341293	CTTCCTCCCTTCCAT[A/G]TCATTTAAAGGGACC	55779
rs2054823	snp	C/T	0.5	9.29588e-05	utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant	SPICE1, CFAP44	GRCh38.p7	3:113445262	TAATAATTTATTACT[C/T]CCCTTTCCCTGCTCT	55779
rs2087129	snp	A/T	0.356383	0.226236	intron-variant	CFAP44, CFAP44-AS1	GRCh38.p7	3:113423922	CAGATGCCAAGCTGT[A/T]ACCAATTCGGCTATT	55779
rs2129430	snp	C/G	0.495252	0.0484902	intron-variant, upstream-variant-2KB	SPICE1, CFAP44	GRCh38.p7	3:113446926	CTCCCACAACATGGG[C/G]GAATTCTGGGAGATA	55779
rs2129431	snp	A/T	0.113685	0.209567	intron-variant, upstream-variant-2KB	SPICE1, CFAP44	GRCh38.p7	3:113446923	ccacaacatgggcga[A/T]ttctgggagatacaa	55779
rs2129432	snp	C/T	0.149665	0.228982	intron-variant, upstream-variant-2KB	SPICE1, CFAP44	GRCh38.p7	3:113445980	TATAGTTCCTTTGAG[C/T]GGTTATGGTAAATTG	55779
rs2129433	snp	A/G	0.475081	0.108804	intron-variant, upstream-variant-2KB	CFAP44	GRCh38.p7	3:113381276	TATTAAGTGATTAAA[A/G]ATTAATAATTATTAA	55779
rs2129434	snp	A/C	0.274929	0.248754	intron-variant, upstream-variant-2KB	CFAP44, CFAP44-AS1	GRCh38.p7	3:113419916	GCCAACACCATGCAC[A/C]GTATTGTGGGTTCAC	55779
rs2171293	snp	C/T	0.484632	0.086302	intron-variant, upstream-variant-2KB	CFAP44	GRCh38.p7	3:113381495	CTCATCCTCTATCTG[C/T]CTCAGTTTAACAAAC	55779
rs2171294	snp	C/T			synonymous-codon, intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	CFAP44, CFAP44-AS1	GRCh38.p7	3:113426161	ATGCCTTTTGTGACT[C/T]TGGATTCAAACATAC	55779
rs2220305	snp	C/T	0.491316	0.0653198	intron-variant, upstream-variant-2KB	CFAP44	GRCh38.p7	3:113435355	cacttctccttgctg[C/T]caccatgtgaagaaa	55779
rs2270781	snp	A/G	0.356414	0.226221	missense, nc-transcript-variant	CFAP44	GRCh38.p7	3:113296813	GTATTAACAGAAAGC[A/G]TTTGAAGGGCTTCTA	55779
rs2270782	snp	A/G	0.388999	0.207796	intron-variant	CFAP44	GRCh38.p7	3:113304149	AATCAAAAGAAAATA[A/G]ACAAAAACACAGATT	55779
rs2270783	snp	G/T	0.384209	0.210922	intron-variant	CFAP44	GRCh38.p7	3:113304828	TTCCAAAGTGCTAAT[G/T]GGCCACAGGGAAATA	55779
rs2270784	snp	A/G	0.0475328	0.146653	intron-variant	CFAP44	GRCh38.p7	3:113305155	CCACAATTTTCACCT[A/G]TAGAAAGCCCCGTGT	55779
rs2270785	snp	C/T	0.380141	0.213456	intron-variant	CFAP44	GRCh38.p7	3:113305171	TAGAAAGCCCCGTGT[C/T]GTGAAATGGTGACAA	55779
rs2291412	snp	A/G	0.0876345	0.190099	intron-variant, upstream-variant-2KB	CFAP44, CFAP44-AS1, MIR8076	GRCh38.p7	3:113433764	GGATTATTGACACAC[A/G]TGGTGTTTGGTGCTA	55779
rs2291413	snp	A/T	0.378962	0.21417	intron-variant, upstream-variant-2KB	CFAP44, CFAP44-AS1, MIR8076	GRCh38.p7	3:113433749	CCTAACATATTTCAT[A/T]AGCACCAAACACCAT	55779
rs2291905	snp	C/T	0.336285	0.234638	missense, nc-transcript-variant	CFAP44	GRCh38.p7	3:113291619	GTGGGAGGATAAGAC[C/T]GCCTTTCCTACGCAA	55779
rs2306792	snp	C/T	0.0581099	0.160244	intron-variant, utr-variant-3-prime	CFAP44	GRCh38.p7	3:113362988	TGGGCATCTTTTAAT[C/T]TGTATGTGGGGTTTA	55779
rs2399476	snp	C/T	0.0790655	0.182432	utr-variant-3-prime, nc-transcript-variant	CFAP44, BOC	GRCh38.p7	3:113287105	CCGCGCCAGCCTGTG[C/T]GGTGCTTTCCTGGGT	55779
rs2650095	snp	C/T	0.107341	0.205301	utr-variant-3-prime, nc-transcript-variant	CFAP44	GRCh38.p7	3:113288756	GGTCTGTGAGCCATG[C/T]GCTAAATTTCTCTTT	55779
rs2650099	snp	C/T	0.0433465	0.140692	intron-variant	CFAP44	GRCh38.p7	3:113297585	TTATCAGATGTGCTG[C/T]CTTTCCATGGAGGCT	55779
rs2895413	snp	C/T	0.472522	0.113946	intron-variant	CFAP44	GRCh38.p7	3:113319095	CGTATCAATACTAAC[C/T]TTGAATGTAAATGGG	55779
rs2936722	snp	A/G	0.0376037	0.131863	intron-variant	CFAP44	GRCh38.p7	3:113317799	gggccagtccagaaa[A/G]gatgttgcatatctc	55779
rs2936812	snp	A/G	0.381697	0.212499	intron-variant	CFAP44	GRCh38.p7	3:113295217	AGGTAGCTGGCTTGA[A/G]TGGCCACACATCTGT	55779
rs3221400	microsatellite	(CA)17/19/20/21/22/23/24/26	0.72827	0.162647	intron-variant	CFAP44	GRCh38.p7	3:113353497	ATATATGTATGAATA[(CA)17/19/20/21/22/23/24/26]AAAACTTATATATAC	55779
rs3732806	snp	A/T	0.422158	0.181278	intron-variant, upstream-variant-2KB	CFAP44	GRCh38.p7	3:113434563	ATATGAAAAGCTGCA[A/T]TATAGACAGAGGGCA	55779
rs3732807	snp	C/T	0.170084	0.236883	intron-variant	CFAP44	GRCh38.p7	3:113401869	GTGTTCTTATCACAC[C/T]TGTTCATTGTTACTT	55779
rs3732808	snp	C/T	0.141324	0.225143	intron-variant	CFAP44	GRCh38.p7	3:113401767	GAAACTACTGATCGA[C/T]TAAAGTATTTTCTTT	55779
rs3732809	snp	C/T	0.198944	0.244731	intron-variant	CFAP44	GRCh38.p7	3:113326714	AACTGTAACCTTGTA[C/T]TGTAAAGTACATTGC	55779
rs3732810	snp	A/C	0.196771	0.244268	intron-variant	CFAP44	GRCh38.p7	3:113326368	ACTAAGGGACCTATT[A/C]GATACCTTATTTTTT	55779
rs3773696	snp	A/C	0.0599851	0.162463	intron-variant	CFAP44	GRCh38.p7	3:113305361	CTCTGGAGTCATAGA[A/C]ATGACTGAAGAGTGA	55779
rs3773697	snp	A/G	0.160938	0.233598	intron-variant	CFAP44	GRCh38.p7	3:113304662	AATGACCTTTGCTTA[A/G]TCTCTACTCATTGGT	55779
rs3814407	snp	A/G	0.255503	0.249939	utr-variant-3-prime, nc-transcript-variant	CFAP44	GRCh38.p7	3:113290519	CTCAATGAGTAGCTC[A/G]TTAATACAGAGCTCT	55779
rs3814408	snp	A/G	0.0941369	0.195465	utr-variant-3-prime, nc-transcript-variant	CFAP44	GRCh38.p7	3:113290541	CAGAGCTCTTAATCT[A/G]AAGAGCTATGCTCTG	55779
rs3829889	snp	A/G	0.277067	0.24853	intron-variant, downstream-variant-500B	CFAP44	GRCh38.p7	3:113296617	CCAAAGGGGGCTCGC[A/G]GACCAGCTCCAGCTA	55779
rs3841612	in-del	-/T	0.114387	0.210022	intron-variant, upstream-variant-2KB	SPICE1, CFAP44	GRCh38.p7	3:113446312	AGCTTCCCATATATT[-/T]ACGGCAGGACACACA	55779
rs3856721	snp	C/T			intron-variant	CFAP44	GRCh38.p7	3:113360275	TGGCCATGTTATTAT[C/T]AAGTGAGATACACCA	55779
rs3856722	snp	C/T	0.031825	0.122064	intron-variant	CFAP44	GRCh38.p7	3:113392602	aaatgcttgaggtga[C/T]ggatatcccatttac	55779
rs3912553	snp	A/C	0.165527	0.235296	intron-variant	CFAP44	GRCh38.p7	3:113388910	AAGAAAGAGATCAAC[A/C]CCAATACAACAATAG	55779
rs3995906	in-del	-/TAT			intron-variant	CFAP44	GRCh38.p7	3:113360272	ACATGGCCATGTTAT[-/TAT]CAAGTGAGATACACC	55779
rs4103250	snp	C/T	0.165527	0.235296	intron-variant	CFAP44	GRCh38.p7	3:113389061	CTTTTTATCCAATGG[C/T]TGCAGAATACACATT	55779
rs4530499	snp	A/C	0	0	intron-variant	CFAP44, CFAP44-AS1	GRCh38.p7	3:113430371	atgtaagaaaagaac[A/C]aaagtcaaaaaaaat	55779
rs4619761	snp	A/T	0.103082	0.202275	intron-variant, upstream-variant-2KB	SPICE1, CFAP44	GRCh38.p7	3:113446441	TGGCTTGTTTTTCCT[A/T]AAAAGGTAAATTAGT	55779
rs4682133	snp	A/G	0.387263	0.208947	intron-variant	CFAP44	GRCh38.p7	3:113344139	CCAGGAATCTAAAAC[A/G]AACCACTGCCTAGAA	55779
rs4682134	snp	C/T	0.474992	0.108989	intron-variant	CFAP44	GRCh38.p7	3:113346330	tgtctagctaaagga[C/T]tgtaagtgcaccaat	55779
rs4682135	snp	G/T	0.0298908	0.118541	intron-variant	CFAP44	GRCh38.p7	3:113390880	tattccatattcata[G/T]attggaagaatcaat	55779
rs4682136	snp	C/T	0.378765	0.214288	intron-variant	CFAP44, CFAP44-AS1	GRCh38.p7	3:113424493	AATCAATATAATATA[C/T]TAATAATCATTAAAG	55779
rs4682137	snp	C/T	0.330947	0.236533	intron-variant, utr-variant-5-prime	CFAP44, CFAP44-AS1	GRCh38.p7	3:113424636	TAATGGGGGCCATCC[C/T]AGCAAGGCAGAATTT	55779
rs4682138	snp	C/T	0.497933	0.032082	intron-variant, downstream-variant-500B	CFAP44, CFAP44-AS1, MIR8076	GRCh38.p7	3:113431959	TTTCTTCCATTGCAG[C/T]CTATGAAGTCCTTCC	55779
rs4682484	snp	C/T	0.055846	0.157494	missense, nc-transcript-variant	CFAP44	GRCh38.p7	3:113304023	TCCTCCTGGAGCTCA[C/T]GGATTCGTTCTTGCA	55779
rs4682485	snp	C/T	0.34303	0.232046	intron-variant	CFAP44	GRCh38.p7	3:113357883	ATATCCATCAAAAAA[C/T]GTACACAATGTTCAT	55779
rs4682486	snp	A/C/T	0.489142	0.0728777	intron-variant	CFAP44	GRCh38.p7	3:113390499	aagttctagatagag[A/C/T]aatcagataagaaag	55779
rs4682487	snp	A/C	0.487432	0.0782705	intron-variant	CFAP44	GRCh38.p7	3:113391356	caaaatggattaaag[A/C]cttaaacttaagacc	55779
rs5022662	snp	A/T	0.489962	0.0701312	intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	CFAP44, BOC	GRCh38.p7	3:113286907	TATTGTTTTTTTTTT[A/T]AAAAAAAAAAGAAGA	55779
rs5851892	in-del	-/A	0.0358304	0.128963	intron-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	CFAP44, BOC	GRCh38.p7	3:113286907	TATTGTTTTTTTTTT[-/A]AAAAAAAAAAGAAGA	55779
rs5851893	in-del	-/G			intron-variant	CFAP44	GRCh38.p7	3:113384696	ACACCTTGATTTGGG[-/G]CTTCTAGCCTCCAGA	55779
rs6438136	snp	G/T	0.0551013	0.156571	intron-variant, downstream-variant-500B	CFAP44	GRCh38.p7	3:113293662	AACCTTCTCAAACAC[G/T]GCCTTGATCCTTCAC	55779
rs6438137	snp	A/G	0.409041	0.192888	intron-variant	CFAP44	GRCh38.p7	3:113299857	acatagcaagatccc[A/G]tctctacaaaaacaa	55779

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