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
rs9521	snp	C/G	0.471004	0.116864	utr-variant-3-prime	SH3PXD2A	GRCh38.p7	10:103598701	CTGAAGGATACTGCC[C/G]GCAGCAGGCAGAGGA	9644
rs10879	snp	C/T	0.417845	0.185278	utr-variant-3-prime	SH3PXD2A	GRCh38.p7	10:103594799	CTGGTATGAATTAGA[C/T]TGGGTGTGATGAACA	9644
rs725076	snp	A/C	0.331179	0.236453	intron-variant	SH3PXD2A	GRCh38.p7	10:103821507	GCTGATGGAGATTGT[A/C]AAGGTGGGGATTAAG	9644
rs725077	snp	C/T	0.480775	0.0961398	intron-variant	SH3PXD2A	GRCh38.p7	10:103821490	AGGTGGGGATTAAGC[C/T]TCCCTTGGCACTGCC	9644
rs728713	snp	A/G	0.204803	0.245881	intron-variant	SH3PXD2A	GRCh38.p7	10:103792691	CCCTGGCCCTGGAGC[A/G]CATGCCCTTAGCCAC	9644
rs743240	snp	A/G	0.0696718	0.173152	intron-variant	SH3PXD2A	GRCh38.p7	10:103819836	GGGGTCCCTAGAGGA[A/G]GGGGGGAGATGGGAG	9644
rs743241	snp	A/G	0.491421	0.0649309	intron-variant	SH3PXD2A	GRCh38.p7	10:103757404	TGACTGAGACCATGA[A/G]AAGAGACAGGCTTTT	9644
rs743244	snp	A/G	0.00318978	0.0398085	intron-variant	SH3PXD2A	GRCh38.p7	10:103834561	aattcccataccata[A/G]gaccaattcacttaa	9644
rs743245	snp	C/G	0.472241	0.114494	intron-variant	SH3PXD2A	GRCh38.p7	10:103822550	ATGAGGGCATGGTGG[C/G]GGGGGAGCAGCACTT	9644
rs743246	snp	C/G	0.435837	0.167226	intron-variant	SH3PXD2A	GRCh38.p7	10:103822548	CCATGAGGGCATGGT[C/G]GGGGGGGAGCAGCAC	9644
rs746472	snp	C/G	0.117886	0.21224	intron-variant	SH3PXD2A	GRCh38.p7	10:103658043	CAAATTGGTTAAACT[C/G]CCTTCTACTGCATGG	9644
rs752681	snp	A/T	0.445724	0.155538	intron-variant	SH3PXD2A	GRCh38.p7	10:103742956	TGCGTGTCACCCTTG[A/T]GGGGGGGAGGGAGGT	9644
rs754591	snp	A/G	0.0130921	0.0798413	intron-variant	SH3PXD2A	GRCh38.p7	10:103720779	GGCTGACAGGCTGCC[A/G]ACGTGTCAGCCTAGT	9644
rs762030	snp	C/G	0.478271	0.101943	intron-variant	SH3PXD2A	GRCh38.p7	10:103820029	TAGTCACTCTGAACT[C/G]TCCAAAAATGAGCAG	9644
rs762031	snp	C/T	0.489665	0.0711382	intron-variant	SH3PXD2A	GRCh38.p7	10:103819697	CTATTCCTCCTTCAG[C/T]CCTTAGATCTCCCCG	9644
rs762032	snp	A/C	0.231189	0.249291	intron-variant	SH3PXD2A	GRCh38.p7	10:103854996	GCACCCCCGCCCCCC[A/C]GGTTTCTTTTTTTGG	9644
rs762033	snp	G/T	0.23031	0.249223	intron-variant	SH3PXD2A	GRCh38.p7	10:103840983	TTCTCATCCTCAGAG[G/T]AGATTTGTATCCCTG	9644
rs762034	snp	C/T	0.00517822	0.0506191	intron-variant	SH3PXD2A	GRCh38.p7	10:103834696	CTGGCATAAAAGCAA[C/T]GTTAATGGTAAAAAT	9644
rs762035	snp	A/G	0.48328	0.0898909	intron-variant	SH3PXD2A	GRCh38.p7	10:103833472	TATATAGATATAAAT[A/G]TATATATATATGTCT	9644
rs762036	snp	C/T	0.0107246	0.0724382	intron-variant	SH3PXD2A	GRCh38.p7	10:103822926	ACGTGATTGTTTCTG[C/T]CAGCCAGATAGAAAA	9644
rs872998	snp	C/G	0.492679	0.0600586	intron-variant	SH3PXD2A	GRCh38.p7	10:103770732	TGACTGACAGGGGGA[C/G]CAGCTCCGGGGCTCT	9644
rs879543	snp	A/G	0.448066	0.152544	intron-variant	SH3PXD2A	GRCh38.p7	10:103741099	CCTTGACCATTCTCT[A/G]AATTCTTCTCTAGGC	9644
rs879544	snp	A/G	0.425432	0.178112	intron-variant	SH3PXD2A	GRCh38.p7	10:103740762	ATGAATGGCGTTCCA[A/G]GTGGCAGAAAGACAG	9644
rs879655	snp	C/T	0.200492	0.245049	intron-variant	SH3PXD2A	GRCh38.p7	10:103666921	TCTGGGAGGGGCATG[C/T]TGCAGGGACACAGCC	9644
rs880549	snp	A/G	0.293807	0.246132	intron-variant	SH3PXD2A	GRCh38.p7	10:103646371	CTAGGGGAGTATCTG[A/G]TTTGAGTGTGGCCTT	9644
rs880868	snp	C/G	0.135825	0.222405	intron-variant	SH3PXD2A	GRCh38.p7	10:103645624	CCCACAGGCTAATCA[C/G]CAGGAACGGGCCGAC	9644
rs880869	snp	A/G	0.135143	0.222054	intron-variant	SH3PXD2A	GRCh38.p7	10:103645632	CTAATCACCAGGAAC[A/G]GGCCGACATTCCTGG	9644
rs902993	snp	A/G	0.152001	0.229992	intron-variant	SH3PXD2A	GRCh38.p7	10:103652793	TCCTGTGAGTGGGCA[A/G]CCCTGGAGATCCTCT	9644
rs902994	snp	A/C	0.299664	0.245017	intron-variant	SH3PXD2A	GRCh38.p7	10:103652715	CAGGTCTCTCACCCC[A/C]CTCCCCGGCTGAAGT	9644
rs902995	snp	A/G	0.124144	0.21601	intron-variant	SH3PXD2A	GRCh38.p7	10:103649657	GATCAGGGGTAGCAT[A/G]CAGGTTGGCAAGGAT	9644
rs902996	snp	A/G	0.353803	0.227431	intron-variant	SH3PXD2A	GRCh38.p7	10:103624734	CATCTCTACCCCAGC[A/G]CTATGGCCATCCCAT	9644
rs902997	snp	C/T	0.297128	0.245518	intron-variant	SH3PXD2A	GRCh38.p7	10:103624505	TGGGAGTTGAGACTT[C/T]CTTGTCCACTGACAG	9644
rs911543	snp	C/T	0.229429	0.249152	intron-variant	SH3PXD2A	GRCh38.p7	10:103787093	TGTCTGGAGTTCAGA[C/T]AGGCTTGATAAGTGA	9644
rs911544	snp	C/T	0.311369	0.242351	intron-variant	SH3PXD2A	GRCh38.p7	10:103771936	GCTCTGCTGGTTTAT[C/T]CTGGTGGTGGGATTA	9644
rs911546	snp	G/T	0.318896	0.240319	intron-variant	SH3PXD2A	GRCh38.p7	10:103771232	AAAATGTCAAGTTTT[G/T]GTAGCCTAACTCCCT	9644
rs923799	snp	A/G	0.499989	0.00239614	intron-variant	SH3PXD2A	GRCh38.p7	10:103708137	ATCTGGCTCTTCTGG[A/G]ACAAGGGACACATGA	9644
rs923800	snp	C/T	0.0154538	0.0865337	intron-variant	SH3PXD2A	GRCh38.p7	10:103696431	TGCCCTATAACCAGT[C/T]CCAGTCTGGCAGGAC	9644
rs923801	snp	C/T	0.0577344	0.159793	intron-variant	SH3PXD2A	GRCh38.p7	10:103696532	CTCCAATCCACACTC[C/T]GTCCTTGCTCCAAGT	9644
rs927345	snp	A/G	0.0178098	0.0926698	intron-variant	SH3PXD2A	GRCh38.p7	10:103815405	ATATAAATACATATA[A/G]TGTATAATATATACA	9644
rs927346	snp	C/T	0.217551	0.247885	intron-variant	SH3PXD2A	GRCh38.p7	10:103815161	tttggtgtcatgtct[C/T]agaaacccttgacta	9644
rs927347	snp	A/G	0.486332	0.08153	intron-variant	SH3PXD2A	GRCh38.p7	10:103814973	CCCAGTTGGCCTGCC[A/G]CACTTTGCCTTCTGC	9644
rs958763	snp	A/T	0.297128	0.245518	intron-variant	SH3PXD2A	GRCh38.p7	10:103789762	TTGGAATGCAGTTGC[A/T]GCCTCTGCCACCTCC	9644
rs972069	snp	C/T	0.394721	0.203852	intron-variant	SH3PXD2A	GRCh38.p7	10:103729608	CATTCTCCAGGGACC[C/T]GCATAGTTCCAGCAG	9644
rs1005113	snp	A/G	0.233235	0.249437	intron-variant	SH3PXD2A	GRCh38.p7	10:103849888	GGATTCTCAGAACTC[A/G]AGAGGAGTAAGTGGG	9644
rs1005114	snp	A/G	0.00438332	0.0466095	intron-variant	SH3PXD2A	GRCh38.p7	10:103850363	CAACAGCCTTGAAGG[A/G]TGTGGTTGGTTGTTC	9644
rs1008463	snp	C/T	0.196149	0.244131	intron-variant	SH3PXD2A	GRCh38.p7	10:103799515	TGTGTGGAAAGGGGA[C/T]ACGCAAGCAGGGAGC	9644
rs1009485	snp	G/T	0.0187191	0.0949165	missense	SH3PXD2A	GRCh38.p7	10:103612942	ATGCCTCCAATGGCA[G/T]TGCCGTGGGCGTTCC	9644
rs1015037	snp	A/C	0.147321	0.227941	intron-variant	SH3PXD2A	GRCh38.p7	10:103787759	TTGCCAAACAGGAAG[A/C]ATGAGGCTGGTGTTT	9644
rs1022735	snp	G/T	0.0221141	0.102801	intron-variant	SH3PXD2A	GRCh38.p7	10:103825660	GGAGAGTCTCTAGGG[G/T]CATGCCACAGGACTC	9644
rs1040863	snp	C/T	0.227369	0.248974	intron-variant	SH3PXD2A	GRCh38.p7	10:103796400	GGTCTCTCTCTCTCT[C/T]TTTTTTTTTTTTTTT	9644
rs1076813	snp	C/T	0.489201	0.0726845	intron-variant	SH3PXD2A	GRCh38.p7	10:103757894	GTCAGCTCTTCCCAC[C/T]GCAGCCCAGGCCGCA	9644
rs1076814	snp	A/G	0.48679	0.0801892	intron-variant	SH3PXD2A	GRCh38.p7	10:103757825	CCTGTGGTAACTTGC[A/G]AAGCAGCAAGGAGCT	9644
rs1078287	snp	C/G	0.473451	0.112115	intron-variant	SH3PXD2A	GRCh38.p7	10:103720157	CTCTAGCTGTGTCCT[C/G]CCATGGCAGAAGGGG	9644
rs1107300	snp	C/T	0.421368	0.182025	intron-variant	SH3PXD2A	GRCh38.p7	10:103777591	TAAGCAAAGATGTGC[C/T]GGAGGATGCAATCCC	9644
rs1389189	snp	C/T	0.429987	0.173507	intron-variant	SH3PXD2A	GRCh38.p7	10:103726319	CGACACTCACAGACT[C/T]ACTGTACTTGGCCCA	9644
rs1472187	snp	C/G	0.222333	0.248464	intron-variant	SH3PXD2A	GRCh38.p7	10:103673434	CTGGGACCACAGGTA[C/G]GCACCACCACGCCTG	9644
rs1473727	snp	C/T	0.232943	0.249417	intron-variant	SH3PXD2A	GRCh38.p7	10:103853940	GAGTTGTTTCTTTTG[C/T]GTCATCTGGTCCAGC	9644
rs1473728	snp	C/G	0.233235	0.249437	intron-variant	SH3PXD2A	GRCh38.p7	10:103853895	GCTGTTACAAGAAAG[C/G]TCTTTTTGGAGGGCT	9644
rs1493171	snp	A/G	0.158962	0.232835	intron-variant	SH3PXD2A	GRCh38.p7	10:103653152	TGCGAAGAGACATGT[A/G]ACAAGTAAACCAAGG	9644
rs1493172	snp	C/G	0.153	0.230415	intron-variant	SH3PXD2A	GRCh38.p7	10:103653080	CAGGCGCTGTGGAGA[C/G]GTCAGCAGCAGGGAG	9644
rs1493173	snp	A/G	0.290201	0.246747	intron-variant	SH3PXD2A	GRCh38.p7	10:103650624	GTAGGCCTTGAACAA[A/G]GGGCAGGCCCCAGGT	9644
rs1493174	snp	A/G	0.0581099	0.160244	intron-variant	SH3PXD2A	GRCh38.p7	10:103698379	GAAGGACACACACAC[A/G]AACTTCCAGCCTGAT	9644
rs1565704	snp	A/G	0.0901694	0.192235	intron-variant	SH3PXD2A	GRCh38.p7	10:103665642	GGCAGCCGGGCGGGC[A/G]GGAGCTGCGAGCAGG	9644
rs1565705	snp	A/G	0.495782	0.0457324	intron-variant, upstream-variant-2KB	SH3PXD2A	GRCh38.p7	10:103680395	gctactcgggagggc[A/G]aagaaggattgttga	9644
rs1565706	snp	C/G	0.408871	0.193029	intron-variant	SH3PXD2A	GRCh38.p7	10:103698275	AGTACCTGCCAGGTG[C/G]AGTTCTGCTGAATGC	9644
rs1565707	snp	A/G	0.424814	0.178718	intron-variant	SH3PXD2A	GRCh38.p7	10:103610232	CCTGGCTGTGCAGCC[A/G]TGCATGTGAGCAGAC	9644
rs1570220	snp	C/T	0.490563	0.0680388	intron-variant	SH3PXD2A	GRCh38.p7	10:103802129	AAAAGTGTAAACATC[C/T]GAGCCCTCAAAACCC	9644
rs1812258	snp	A/G	0.216349	0.247725	intron-variant	SH3PXD2A	GRCh38.p7	10:103779104	tccagcctgggcgac[A/G]gagcaagactccatc	9644
rs1884932	snp	A/G	0.116838	0.211584	intron-variant	SH3PXD2A	GRCh38.p7	10:103613353	TGGCACCGAGGGTAG[A/G]TGGAAAAGACACCCA	9644
rs1963711	snp	C/T	0.00517822	0.0506191	intron-variant	SH3PXD2A	GRCh38.p7	10:103825939	tatctctactaaaaa[C/T]acaaaaaattagccg	9644
rs1963712	snp	A/G	0.00517822	0.0506191	intron-variant	SH3PXD2A	GRCh38.p7	10:103825912	gccgggcgtggtggc[A/G]ggagcctgtagtccc	9644
rs1963713	snp	C/T	0.00517822	0.0506191	intron-variant	SH3PXD2A	GRCh38.p7	10:103825833	gagcttgcggtgagc[C/T]gagattgcgccactg	9644
rs1994838	snp	C/T	0.41408	0.188621	intron-variant	SH3PXD2A	GRCh38.p7	10:103696168	CAGGCTGTGACTGAA[C/T]GGTGGGAACGAAGAG	9644
rs1994839	snp	C/T	0.172997	0.237846	intron-variant	SH3PXD2A	GRCh38.p7	10:103677676	TAAGCACCTACTATG[C/T]GCTATGCGCTTGCTA	9644
rs1998294	snp	A/G	0.442249	0.159814	intron-variant, nc-transcript-variant	SH3PXD2A, SH3PXD2A-AS1	GRCh38.p7	10:103754244	ACTCCATCCTGGGTG[A/G]CAGAGTGCGACCCTG	9644
rs2013456	snp	A/G	0.309894	0.242719	intron-variant	SH3PXD2A	GRCh38.p7	10:103771634	GATTCTCCTGCCTCA[A/G]CTGGGACTACAGATG	9644
rs2019970	snp	C/G	0.394904	0.203722	intron-variant	SH3PXD2A	GRCh38.p7	10:103728988	gagaatcgcttgaac[C/G]cggcgagggggaggc	9644
rs2047036	snp	A/G	0.432357	0.171014	intron-variant	SH3PXD2A	GRCh38.p7	10:103717405	TCCAGACTCAGCTTG[A/G]GCCCCTCCTCCAGAA	9644
rs2047037	snp	A/G	0.177182	0.23916	intron-variant	SH3PXD2A	GRCh38.p7	10:103717342	TGGGATCTGTTTATG[A/G]ATCTCTCCCCACCAA	9644
rs2047038	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	SH3PXD2A	GRCh38.p7	10:103663698	TTTGGGTCCTTCTGT[A/G]GGGGGAGGCTCCCTC	9644
rs2065011	snp	A/C	0.00517822	0.0506191	intron-variant	SH3PXD2A	GRCh38.p7	10:103827381	TAGACACTCCATTTC[A/C]GTAGTGTTACCGGGA	9644
rs2065012	snp	C/T	0.488726	0.0742286	intron-variant	SH3PXD2A	GRCh38.p7	10:103805838	CAGAGCCTCACTATG[C/T]TGTCCAGGCCAGTCT	9644
rs2067560	snp	C/T	0.31721	0.240796	intron-variant	SH3PXD2A, SH3PXD2A-AS1	GRCh38.p7	10:103750986	GTCCGTTTCCCGCTG[C/T]GGTGTTCTGCGGCAG	9644
rs2073339	snp	C/T	0.188	0.24219	intron-variant	SH3PXD2A	GRCh38.p7	10:103784225	GAAGTCCAGGGAGGG[C/T]GGGACCTGGAAAAGG	9644
rs2073340	snp	C/G	0.416055	0.186885	intron-variant	SH3PXD2A	GRCh38.p7	10:103783998	CAAGCTTTGCGGGGG[C/G]ACTTTTCCTGTTGCA	9644
rs2073341	snp	C/T	0.490782	0.0672626	intron-variant	SH3PXD2A	GRCh38.p7	10:103783635	CCAAGCAGCAGATGC[C/T]AGCTTTGACACCTTC	9644
rs2078244	snp	C/T	0.498182	0.0300969	intron-variant, upstream-variant-2KB	SH3PXD2A	GRCh38.p7	10:103681772	CATTTTGTGTGTGTG[C/T]GCGCGCGCGCGCGGG	9644
rs2093355	snp	A/G	0.219947	0.248187	intron-variant	SH3PXD2A	GRCh38.p7	10:103777988	GCATGGTCCTATTTT[A/G]CAGATGAGTAGACTG	9644
rs2093356	snp	C/T	0.00517822	0.0506191	intron-variant	SH3PXD2A	GRCh38.p7	10:103832546	ATTCCATGGTGTATA[C/T]GTGCCACATCTTCTT	9644
rs2131471	snp	C/T	0.117537	0.212022	intron-variant, upstream-variant-2KB	SH3PXD2A	GRCh38.p7	10:103624215	GCACCCAGACCCTGT[C/T]CCCTCCCCACATCCC	9644
rs2131472	snp	A/G	0	0	intron-variant	SH3PXD2A	GRCh38.p7	10:103703476	AGTTGTGAAACACTA[A/G]GCAGGGCAGGAGGGG	9644
rs2145309	snp	A/G	0.285257	0.247501	intron-variant	SH3PXD2A	GRCh38.p7	10:103690367	GAACCAATGGGAGGT[A/G]CATAGAGAGCTTGAA	9644
rs2145310	snp	C/T	0.47666	0.105476	intron-variant	SH3PXD2A	GRCh38.p7	10:103704127	CCCTGCTGCCAGCAC[C/T]GGTTCACCCTCGAGA	9644
rs2172459	snp	A/G	0.493793	0.055364	intron-variant	SH3PXD2A	GRCh38.p7	10:103658747	GCCATGTTCAGGGAA[A/G]CTCTTTCTACCCGAC	9644
rs2180991	snp	A/G	0.00438332	0.0466095	intron-variant	SH3PXD2A	GRCh38.p7	10:103851883	AACAAACAAGAAATT[A/G]TATCTATTTGGATTT	9644
rs2224375	snp	C/G	0.286042	0.247388	intron-variant	SH3PXD2A	GRCh38.p7	10:103693317	cgccccagcccgccc[C/G]gcTAACTGGGGCTCA	9644
rs2224507	snp	A/G	0.249038	0.249998	intron-variant	SH3PXD2A	GRCh38.p7	10:103823408	TCCCAACCCTGTAAG[A/G]GCAGTGGTTAAAGCC	9644
rs2236279	snp	G/T	0.202651	0.245475	intron-variant	SH3PXD2A	GRCh38.p7	10:103772003	GTGCTTCCGTTTTCC[G/T]CGGCCAGTGGTCCAT	9644
rs2236280	snp	A/C	0.302686	0.244385	intron-variant	SH3PXD2A	GRCh38.p7	10:103771804	GGCTCCTTGATGTGA[A/C]GGCTGCAGGGTATGT	9644
rs2281584	snp	A/G	0.477768	0.103061	utr-variant-3-prime	SH3PXD2A	GRCh38.p7	10:103599223	CAGTCCTGCATTTTA[A/G]TGACTCTATTACTTA	9644

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