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
rs869884	snp	C/T	0.431029	0.17242	intron-variant, upstream-variant-2KB	PSTPIP1	GRCh38.p7	15:76999257	GTCCATCTCCCTTCC[C/T]GAACCCATTTTTTAC	9051
rs1022197	snp	A/G	0.472989	0.113031	intron-variant, upstream-variant-2KB	PSTPIP1	GRCh38.p7	15:76997700	TCTTTTGGCTTCGGG[A/G]TAAGATAAGAGGTAA	9051
rs1022198	snp	C/T	0.484138	0.0876334	intron-variant, upstream-variant-2KB	PSTPIP1	GRCh38.p7	15:76997820	AGAAAAGGCACACTA[C/T]TCTGGCCACAGGTGT	9051
rs1141038	snp	C/G	0	0	missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB	PSTPIP1	GRCh38.p7	15:77018463	GAGGCAGAGGGCCCA[C/G]GCGGAGGAGCGGTAC	9051
rs1141039	snp	A/G	0	0	missense, nc-transcript-variant, utr-variant-5-prime	PSTPIP1	GRCh38.p7	15:77025566	GAGCTGCGGAGTCTC[A/G]AGGAGTTTCGTGAGA	9051
rs1141040	snp	A/T	0.000118299	0.00768996	synonymous-codon, nc-transcript-variant	PSTPIP1	GRCh38.p7	15:77028565	CCAGTCCAAGAAGAC[A/T]TACGAGCAGAAGTGC	9051
rs1141041	snp	G/T	0	0	missense, nc-transcript-variant	PSTPIP1	GRCh38.p7	15:77028574	GAAGACATACGAGCA[G/T]AAGTGCCGGGACGCG	9051
rs1141042	snp	A/G/T	0.000161987	0.00899818	missense, nc-transcript-variant	PSTPIP1	GRCh38.p7	15:77028582	ACGAGCAGAAGTGCC[A/G/T]GGACGCGGACGACGC	9051
rs1141043	snp	A/G/T	3.79643e-05	0.00435669	missense, nc-transcript-variant	PSTPIP1	GRCh38.p7	15:77028587	CAGAAGTGCCGGGAC[A/G/T]CGGACGACGCGGAGC	9051
rs1141044	snp	G/T	0	0	missense, nc-transcript-variant	PSTPIP1	GRCh38.p7	15:77028601	CGCGGACGACGCGGA[G/T]CAGGCCTTCGAGCGC	9051
rs1141045	snp	C/G	0	0	missense, nc-transcript-variant	PSTPIP1	GRCh38.p7	15:77028604	GGACGACGCGGAGCA[C/G]GCCTTCGAGCGCATT	9051
rs2254441	snp	A/G	0.475348	0.108251	intron-variant	PSTPIP1	GRCh38.p7	15:76995677	TGAAATCTCCATGCA[A/G]GTGATGGGATGCGGC	9051
rs2458249	snp	A/C	0.18	0.24	intron-variant	PSTPIP1	GRCh38.p7	15:77000460	TATATATATATATAT[A/C]TCTCTTTAAATGCCC	9051
rs2458253	snp	A/C/T	0.001245	0.0249246	utr-variant-5-prime, missense, nc-transcript-variant	PSTPIP1	GRCh38.p7	15:76995448	CTTCCCGGCCGGCGC[A/C/T]GTCTGCAACACTCAG	9051
rs2458254	snp	G/T	0.476918	0.104919	upstream-variant-2KB	PSTPIP1	GRCh38.p7	15:76994528	CTCAGTGAATGGGAA[G/T]GGATGGAGAGAGAAA	9051
rs2469198	snp	C/T	0.0399052	0.1355	intron-variant	PSTPIP1	GRCh38.p7	15:77020169	ATGTTGCGTACCTCC[C/T]GCTTCCTGAGGCCCA	9051
rs2469203	snp	A/G	0.483199	0.0901004	intron-variant	PSTPIP1	GRCh38.p7	15:77003793	CAGGATGTCAGGGTC[A/G]TCATCACTTAAGATA	9051
rs2469207	snp	A/G	0.046775	0.145601	intron-variant	PSTPIP1	GRCh38.p7	15:77011659	ATAAATATGGGATGA[A/G]GATGACTTACAGCTG	9051
rs2469229	snp	A/C	0.476052	0.106772	upstream-variant-2KB	PSTPIP1	GRCh38.p7	15:76994352	TTCTCGACACCGTCT[A/C]CTTTCCAAAGACTGG	9051
rs2469230	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	PSTPIP1	GRCh38.p7	15:76998891	CACAGAGGGAGGGAA[A/G]GGATAATGTGATTTC	9051
rs2469231	snp	A/T	0.154661	0.231107	intron-variant	PSTPIP1	GRCh38.p7	15:77006350	aggagttctttatat[A/T]ttctagatactcatc	9051
rs2469232	snp	G/T	0.484701	0.0861117	intron-variant	PSTPIP1	GRCh38.p7	15:77006593	ggtcttacatctagg[G/T]gttcacttcatcttg	9051
rs2469235	snp	A/G	0.148326	0.228391	intron-variant	PSTPIP1	GRCh38.p7	15:77013151	GCACCATGCAGCTCC[A/G]TGCAGCTACCTTCCA	9051
rs2469236	snp	A/C	0.0150606	0.0854603	intron-variant	PSTPIP1	GRCh38.p7	15:77030195	GCTGCCTTCTCTGAA[A/C]CTCAGTTTCCCCTCT	9051
rs2469237	snp	C/T	0.0372196	0.131242	intron-variant	PSTPIP1	GRCh38.p7	15:77030668	TTAAAGGGGCCCAAG[C/T]GAGGCAGTTGGGGAA	9051
rs3812911	snp	C/G	0.37685	0.215428	intron-variant, upstream-variant-2KB	PSTPIP1	GRCh38.p7	15:77018295	GGCAGGAAGCAGGTG[C/G]CTTCCGCTCGGCTCC	9051
rs3812912	snp	A/G	0.105214	0.203807	intron-variant, upstream-variant-2KB	PSTPIP1	GRCh38.p7	15:77018305	AGGTGGCTTCCGCTC[A/G]GCTCCTGGGACAGTG	9051
rs3812913	snp	A/T	0.0391387	0.134304	intron-variant, upstream-variant-2KB	PSTPIP1	GRCh38.p7	15:77018374	GCCCTGCTTTAAAAA[A/T]CTCTTCTGTGTTCCC	9051
rs3812914	snp	C/T	0.0149638	0.0851937	PSTPIP1	15	allele_origin=T(germline)/C(germline)	15:77018543	TCAAGTAAGATCTCC[C/T]GGGCCCTGGGGCTCA	9051
rs3812915	snp	C/G	0.109461	0.206758	intron-variant	PSTPIP1	GRCh38.p7	15:77028146	GGGCTCGTGAATGAA[C/G]GGCAGATGAAGTCAG	9051
rs3812916	snp	A/C/T	0.0541834	0.155422	intron-variant	PSTPIP1	GRCh38.p7	15:77031319	GGTAAGGTAGGGCAG[A/C/T]CTCTAGGCAGCAAAG	9051
rs3841234	in-del	-/TT	0.0836354	0.186609	intron-variant	PSTPIP1	GRCh38.p7	15:77028121	GATGGTCCCGGGCCC[-/TT]CCCTTGTGGGGCTCG	9051
rs3935339	snp	A/G	0.40386	0.197046	intron-variant	PSTPIP1	GRCh38.p7	15:77029688	GAATGAGAGCGCCGC[A/G]CCCATGATTGTGCAG	9051
rs3936040	snp	A/G	0.254385	0.249962	intron-variant	PSTPIP1	GRCh38.p7	15:77022791	AGGTCCCCTGTCCCC[A/G]TTGCTGGAACCATCA	9051
rs4075475	snp	A/G	0.0998734	0.199905	intron-variant, upstream-variant-2KB	PSTPIP1	GRCh38.p7	15:77017078	GGCCTGCCTTGGTGC[A/G]GTTGGTGACAAAAAT	9051
rs4078354	snp	C/T	0.439661	0.162877	intron-variant	PSTPIP1	GRCh38.p7	15:77032539	GGCCTGGGACCCAAC[C/T]CCCCACAACCCCTGC	9051
rs4420499	snp	G/T	0.212728	0.247206	intron-variant	PSTPIP1	GRCh38.p7	15:77022633	AGATCAGAGCTCAAG[G/T]CTGTTCACTTTGGGG	9051
rs4886508	snp	C/T	0.418974	0.184249	intron-variant	PSTPIP1	GRCh38.p7	15:77015569	CAACTAGGGTAGGTC[C/T]CCTGGGGGTGATGCT	9051
rs5021805	snp	A/G	0.217851	0.247924	intron-variant, upstream-variant-2KB	PSTPIP1	GRCh38.p7	15:76997959	GACTGGTTTTTAGGC[A/G]GGGTGCAGTGGTTCA	9051
rs6495232	snp	C/T	0.0221141	0.102801	intron-variant	PSTPIP1	GRCh38.p7	15:77035080	CCCCACCCCTACCCA[C/T]GGGGGAAGCTGCTAG	9051
rs7167993	snp	A/T	0	0	intron-variant	PSTPIP1	GRCh38.p7	15:77000716	CTTTTACAAATTTTT[A/T]Atttttgcagagatg	9051
rs7173067	snp	A/G	0.475702	0.107512	intron-variant	PSTPIP1	GRCh38.p7	15:77016046	CCTCCATAAGGACAG[A/G]AGAAGGGTTCCCTTG	9051
rs7175783	snp	G/T	0.491263	0.0655142	intron-variant	PSTPIP1	GRCh38.p7	15:77010924	GTGCTGGGATTTCAG[G/T]TGTGAGCCACCACGT	9051
rs7176360	snp	G/T	0	0	intron-variant, upstream-variant-2KB	PSTPIP1	GRCh38.p7	15:76998519	CCACAATTTTAATGA[G/T]CTTGGTCATGGGGTC	9051
rs8029854	snp	C/T	0.478271	0.101943	intron-variant	PSTPIP1	GRCh38.p7	15:77021690	TCTTAAAAAAAAAGA[C/T]AGTGTTAGTATTTGC	9051
rs8030698	snp	C/T	0.492188	0.0620098	intron-variant	PSTPIP1	GRCh38.p7	15:77011398	CAGCCCAGGCATCTC[C/T]GGGACTCGGCCAGCT	9051
rs9707978	snp	A/G			intron-variant	PSTPIP1	GRCh38.p7	15:77035236	CTAGGATCCTCCCAA[A/G]GGCCCTGCAGGGAGC	9051
rs9806416	snp	C/T	0.495135	0.0490805	intron-variant	PSTPIP1	GRCh38.p7	15:77035230	GGGGTTCTAGGATCC[C/T]CCCAAGGGCCCTGCA	9051
rs10152353	snp	A/G	0.103082	0.202275	intron-variant	PSTPIP1	GRCh38.p7	15:77030420	CTCCCAGTGGGAGGA[A/G]GCATCCAGGATGGGA	9051
rs10400889	snp	G/T	0	0	downstream-variant-500B	PSTPIP1	GRCh38.p7	15:77037627	CTTGGGGGCGGAGGG[G/T]TGAGCAGGTCCATGG	9051
rs10681693	in-del	-/TA	0	0	intron-variant	PSTPIP1	GRCh38.p7	15:77000477	ATATATATATATATA[-/TA]CACACACACACACAC	9051
rs11072639	snp	A/C	0.228547	0.249078	intron-variant	PSTPIP1	GRCh38.p7	15:77015060	GGCTGTTCATGGGTT[A/C]CCCAGAGCCGCACTC	9051
rs11072640	snp	A/T	0.0356815	0.128715	intron-variant	PSTPIP1	GRCh38.p7	15:77034269	CTGGCCGCTTCCTCC[A/T]CCTGTCCCCAGCCCC	9051
rs11373069	in-del	-/A	1.81299e-05	0.00301075	intron-variant	PSTPIP1	GRCh38.p7	15:77035767	GGCCAGTGTCCCCAG[-/A]AAGGGGAGGGGTCTA	9051
rs11633011	snp	A/C	0	0	intron-variant	PSTPIP1	GRCh38.p7	15:77028658	GGTGGAGAAGGTGCG[A/C]TGGGCTGCTGGGCCG	9051
rs11633907	snp	A/C	0	0	intron-variant	PSTPIP1	GRCh38.p7	15:77013977	CCAGCCTGGCCCCAG[A/C]TGAGGGAAGGTGTTT	9051
rs11636266	snp	C/T	0.0872718	0.189788	intron-variant	PSTPIP1	GRCh38.p7	15:77025789	GGGCAGAGGCCTGGC[C/T]GCTGGCACTAAGGCC	9051
rs11637049	snp	A/C	0	0	intron-variant	PSTPIP1	GRCh38.p7	15:77003724	cctcacccacacttg[A/C]taggtggccttggag	9051
rs11639459	snp	C/T	0.217851	0.247924	intron-variant	PSTPIP1	GRCh38.p7	15:77010628	TGCTCCTTGCCTCCT[C/T]TCTCACTTTTCTTCT	9051
rs11854745	snp	C/G	0.154661	0.231107	intron-variant, downstream-variant-500B	PSTPIP1	GRCh38.p7	15:77036244	CAGCACACACGTGGA[C/G]CACATGTACCTATGC	9051
rs11855392	snp	G/T	0.106278	0.204558	intron-variant	PSTPIP1	GRCh38.p7	15:77033286	GCAGTGGCAACGCTG[G/T]CTGGCTGGAGCAGGA	9051
rs11858480	snp	C/T	0.0941849	0.195504	intron-variant, synonymous-codon, missense, nc-transcript-variant	PSTPIP1	GRCh38.p7	15:77032938	CATACAGCCGTCCTG[C/T]GGCATGATAAAGAGG	9051
rs11858973	snp	A/T	0.11963	0.213316	intron-variant, downstream-variant-500B	PSTPIP1	GRCh38.p7	15:77036339	CTGCAGGTCATAGCT[A/T]GAGGGCCAGGCTCTG	9051
rs12050669	snp	A/G	0	0	intron-variant	PSTPIP1	GRCh38.p7	15:77023728	atgtgcaggccctga[A/G]ctctgggaggggtct	9051
rs12148413	snp	A/G	0.441705	0.160466	intron-variant	PSTPIP1	GRCh38.p7	15:77023792	GAGGGTGGTGTGCGT[A/G]AGGGCTGGGTTGGGG	9051
rs12438566	snp	A/G	0.430285	0.173197	intron-variant	PSTPIP1	GRCh38.p7	15:77034405	CCTGCGCATGTGTGT[A/G]CACTCCTGGGGCCTT	9051
rs12900395	snp	C/G	0.44651	0.154543	intron-variant, upstream-variant-2KB	PSTPIP1	GRCh38.p7	15:77018004	TGTGTAAAGCCAGGT[C/G]TGGAGTCCCAAGAGC	9051
rs12903227	snp	A/C	0.430732	0.172731	intron-variant	PSTPIP1	GRCh38.p7	15:77030688	CAGTTGGGGAAGGTA[A/C]CTGTTACTCACTCGT	9051
rs12905311	snp	C/T	0.49949	0.0159663	intron-variant	PSTPIP1	GRCh38.p7	15:77011969	AGTGCTCCCTCTGCT[C/T]CTGATGGCCCCACAG	9051
rs12906071	snp	A/T	0.0129783	0.0795028	intron-variant	PSTPIP1	GRCh38.p7	15:77025643	GGAGCTGCTCCCCCA[A/T]TGCCAGCCTCTCAGT	9051
rs12908255	snp	C/T	0.499575	0.0145705	intron-variant	PSTPIP1	GRCh38.p7	15:77009016	TACACTCATGGGTGG[C/T]CCTGGGGAGCCCCTC	9051
rs12912465	snp	C/T	0.208169	0.246476	intron-variant, upstream-variant-2KB	PSTPIP1	GRCh38.p7	15:77017118	CCAGCACCTCTCAAG[C/T]TCCCCTGGAGTAAGC	9051
rs12913937	snp	A/G	0.49998	0.00319482	intron-variant	PSTPIP1	GRCh38.p7	15:77023790	TGGAGGGTGGTGTGC[A/G]TAAGGGCTGGGTTGG	9051
rs12915411	snp	A/C			intron-variant	PSTPIP1	GRCh38.p7	15:77014166	ccagctgcacccggc[A/C]ggtccctgggcagat	9051
rs12916725	snp	C/G/T			intron-variant	PSTPIP1	GRCh38.p7	15:77014169	gctgcacccggcagg[C/G/T]ccctgggcagattgg	9051
rs16968616	snp	C/T	0.0941369	0.195465	intron-variant	PSTPIP1	GRCh38.p7	15:77015387	CCCATCTTCGCCTCC[C/T]GAGATCTGTGTTGTG	9051
rs16968623	snp	A/G	0.499693	0.0123764	intron-variant	PSTPIP1	GRCh38.p7	15:77019700	CTCCAGCGAGCTGCC[A/G]TGCAAATCAACAAGA	9051
rs16968625	snp	A/G	0.304688	0.243945	intron-variant	PSTPIP1	GRCh38.p7	15:77020110	ATTTACAGCAGGGAA[A/G]GAGAAGCTACCCACA	9051
rs16968627	snp	C/T	0.0832709	0.186283	intron-variant	PSTPIP1	GRCh38.p7	15:77020485	ATGAAGTACTGTTGA[C/T]GAGGCCATGCAGCTG	9051
rs17380886	snp	C/G	0.43088	0.172575	intron-variant, upstream-variant-2KB	PSTPIP1	GRCh38.p7	15:76998939	ATAAAGAGCATCACA[C/G]CTTGGCAGGAAGTTT	9051
rs17465692	snp	A/G	0.41441	0.188333	intron-variant	PSTPIP1	GRCh38.p7	15:77014919	CACACCATGGACGGC[A/G]AGGGCTGGGTCCCAC	9051
rs17465755	snp	G/T	0.21725	0.247846	intron-variant	PSTPIP1	GRCh38.p7	15:77015411	TGTTGTGGTCAGGAA[G/T]ATAACGCTATGATAC	9051
rs28863174	snp	A/C			intron-variant	PSTPIP1	GRCh38.p7	15:77006053	TTAACTTTTTGAGTA[A/C]CCGCCAAACAGTTTT	9051
rs28939089	snp	A/C/G			missense, intron-variant, nc-transcript-variant	PSTPIP1	GRCh38.p7	15:77032304	CTGCCCCAGCTCTAC[A/C/G]AGGAAGTGCGGCTGA	9051
rs34022353	in-del	-/A			intron-variant	PSTPIP1	GRCh38.p7	15:77023072	TGGGGGCTGGGAAAA[-/A]GGGCCAGCAGCTCCC	9051
rs34066759	in-del	-/A			intron-variant	PSTPIP1	GRCh38.p7	15:77034695	TTCTCTCCTAGTAAA[-/A]GCTTCACTCATCTTT	9051
rs34087066	in-del	-/C			intron-variant	PSTPIP1	GRCh38.p7	15:77005039	TTCCCCAGTGCCTCC[-/C]ATGTGGAACTTTAGC	9051
rs34107915	snp	C/T			intron-variant	PSTPIP1	GRCh38.p7	15:77029627	GGCCTGGGCGGTACT[C/T]CCCACACACACCTCC	9051
rs34127110	snp	A/G	0.427119	0.176434	intron-variant	PSTPIP1	GRCh38.p7	15:77021230	CAGGCCTGGAGGCTC[A/G]GGCCACTGAAATTAA	9051
rs34192860	snp	A/G	0.499598	0.0141716	intron-variant	PSTPIP1	GRCh38.p7	15:77019664	TCGCCTAGCCTCTCC[A/G]AGTTTGTTTCTCACC	9051
rs34220530	snp	C/T	0.404209	0.196773	intron-variant	PSTPIP1	GRCh38.p7	15:77003978	TCAGAATGCCTCCTC[C/T]AATCATGTTCACCAT	9051
rs34224655	in-del	-/C			intron-variant	PSTPIP1	GRCh38.p7	15:77001703	AGACCTGGTGTTCCC[-/C]TGTAAAAAGCAGAGA	9051
rs34240327	snp	C/G	0.0155682	0.0868433	missense, intron-variant, nc-transcript-variant	PSTPIP1	GRCh38.p7	15:77032329	GCGTCTATGCTGCAG[C/G]CTTCCAGCGTCAGCC	9051
rs34316721	in-del	-/G			downstream-variant-500B	PSTPIP1	GRCh38.p7	15:77037569	AGGATGTGGCAGGGG[-/G]CAAGAAGGGGCTCAG	9051
rs34370173	snp	A/G	0.408359	0.193449	intron-variant, upstream-variant-2KB	PSTPIP1	GRCh38.p7	15:76999436	GACGTGCGCCGCCAC[A/G]TCTGTCTAATTTTTG	9051
rs34413462	in-del	-/G			intron-variant	PSTPIP1	GRCh38.p7	15:77020989	CCTGGCCTCCCTGAG[-/G]CCCACAGCTGCCCCC	9051
rs34470467	in-del	-/G			intron-variant	PSTPIP1	GRCh38.p7	15:77018879	CCCCTGCAGCACTGG[-/G]CTCAGCATGGGCTTC	9051
rs34500166	snp	A/C	0.431177	0.172264	intron-variant, upstream-variant-2KB	PSTPIP1	GRCh38.p7	15:77016583	CAGCTGAGCCTGGAC[A/C]AGGCCCTCCTCAGGA	9051
rs34504488	in-del	-/A/GGA			intron-variant	PSTPIP1	GRCh38.p7	15:77027636	GGTCTGCAGCAAGGA[-/A/GGA]CCTCACGGCACACCC	9051
rs34612811	snp	C/T	0.5	0	intron-variant	PSTPIP1	GRCh38.p7	15:77034201	TGGGGAAAAGAGGTG[C/T]GGGGCACGCAGCACA	9051

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