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
rs7067	snp	C/T	0.499942	0.00539106	utr-variant-3-prime	PWP2	GRCh38.p7	21:44131077	GAGACTTATTTATAT[C/T]TTTAACATAAAGGTT	5822
rs756553	snp	C/T	0.398987	0.200768	synonymous-codon	PWP2	GRCh38.p7	21:44118766	CGTTCTCTGCAGCAT[C/T]TCAGATCAGAGCATC	5822
rs756554	snp	A/C	0.395266	0.203476	intron-variant	PWP2	GRCh38.p7	21:44118844	TTCAGGTTTGTCCCC[A/C]GCCTGGGTGGTAGAG	5822
rs756555	snp	A/T	0.472989	0.113031	intron-variant	PWP2	GRCh38.p7	21:44118901	TGCCCGGCTACAGGC[A/T]TACTTGACAGCCACC	5822
rs885872	snp	C/T	0.377977	0.21476	downstream-variant-500B	PWP2	GRCh38.p7	21:44131294	AGCGGGGGCTCTGCC[C/T]TGTGACCTGTGCATA	5822
rs1051979	snp	A/T	0	0	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	TRAPPC10, PWP2	GRCh38.p7	21:44105745	GTGTTTGAGACAAGC[A/T]GGTTTTGTTGATAAA	5822
rs1051981	snp	A/G	0.376592	0.215579	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	TRAPPC10, PWP2	GRCh38.p7	21:44105804	ATGCAATGTGTATCT[A/G]AAAAGCAAGGAATTT	5822
rs1131297	snp	C/T	0	0	synonymous-codon	PWP2	GRCh38.p7	21:44120362	GGTCAAGGTGTGGAA[C/T]ACCCTCAGCGGCTTC	5822
rs1858665	snp	C/T	0.482534	0.0918038	intron-variant	PWP2	GRCh38.p7	21:44117172	GAGTCAAGACTTGAA[C/T]GGGGACTGGAGGAAG	5822
rs2020944	snp	A/G	0.498084	0.0308911	intron-variant	PWP2	GRCh38.p7	21:44122712	TGGGGAGGCTGAGGC[A/G]GGTGGTTTGCTTGAG	5822
rs2020945	snp	A/G	0.407066	0.1945	missense	PWP2	GRCh38.p7	21:44109038	CTAAATTTTACCTGC[A/G]ATGGAAATTCAGTTA	5822
rs2020946	snp	C/G	0.482008	0.0931261	intron-variant	PWP2	GRCh38.p7	21:44109234	TAAGGGAGCCCAGGA[C/G]AGGACTACAGGACAG	5822
rs2071142	snp	A/G	0.44087	0.161458	intron-variant	PWP2	GRCh38.p7	21:44119545	TCCTGTCCCCGTCCC[A/G]TTGGCCTCTGTGCCT	5822
rs2071143	snp	A/G	0.40396	0.196968	synonymous-codon	PWP2	GRCh38.p7	21:44121038	CTCCTGGGACAAGAC[A/G]GTGCGCCTATGGGAC	5822
rs2071144	snp	A/G	0.238749	0.249747	intron-variant	PWP2	GRCh38.p7	21:44121273	GGTTGGCAGTACCTA[A/G]GAGACAGCAGATTGG	5822
rs2071145	snp	A/G	0.161267	0.233723	intron-variant	PWP2	GRCh38.p7	21:44121637	GTACTAGAGGCAGCC[A/G]TGGCCTCCTGTGTTC	5822
rs2071146	snp	A/C	0.482979	0.0906686	intron-variant	PWP2	GRCh38.p7	21:44123139	GGGCTGTGAGGCTCA[A/C]CTGGGTGGGGGTCAG	5822
rs2071147	snp	C/T	0.482979	0.0906686	downstream-variant-500B	PWP2	GRCh38.p7	21:44131355	CTGACCTCTTGGGGA[C/T]GCTTTGGAGTCTGGG	5822
rs2187313	snp	C/T	0.336597	0.234523	synonymous-codon	PWP2	GRCh38.p7	21:44124713	TCTTGCAACCTGTCT[C/T]TGGACGCCATGGAGG	5822
rs2242951	snp	G/T	0.29175	0.246489	intron-variant	PWP2	GRCh38.p7	21:44115121	AGGGGCTGTGCCGGG[G/T]TGTCTTCCTGTGCCT	5822
rs2242952	snp	C/G/T			intron-variant	PWP2	GRCh38.p7	21:44121564	CCGGAAGCCAGATGC[C/G/T]GCTGCCCAGGGATCT	5822
rs2242953	snp	A/G	0.488905	0.0736498	intron-variant	PWP2	GRCh38.p7	21:44125453	GATGGCTTCCTGCCC[A/G]GGGTCCTGTGTACAA	5822
rs2242954	snp	C/G	0.488905	0.0736498	intron-variant, utr-variant-3-prime	PWP2	GRCh38.p7	21:44127682	GGCGTCAAGAGAGGA[C/G]GACGCATGCGTGTAC	5822
rs2243999	snp	C/T	0.406058	0.19531	intron-variant	PWP2	GRCh38.p7	21:44114151	CCCCTGGGGTAGCTG[C/T]GCGGTGGTGACCTCT	5822
rs2251267	snp	C/T	0.482905	0.0908579	intron-variant	PWP2	GRCh38.p7	21:44129992	TAGAGTTCACGTAAG[C/T]GCATTGTTCCTTGGA	5822
rs2299821	snp	A/G	0.00993419	0.0697739	intron-variant	PWP2	GRCh38.p7	21:44117271	GTGTGCCTGCTAGGC[A/G]GGGACTGCGGGCTGT	5822
rs2329707	snp	A/G	0.481396	0.0946345	intron-variant	PWP2	GRCh38.p7	21:44110978	AGTGTCTGGCTTCAA[A/G]CAACAGGCTGACTCT	5822
rs2516519	snp	C/T	0.483852	0.0883933	intron-variant	PWP2	GRCh38.p7	21:44112893	TGATGTATCCAAAGC[C/T]CATTTTTAAGGCTTT	5822
rs2516520	snp	C/T	0.0486741	0.148216	utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B	TRAPPC10, PWP2	GRCh38.p7	21:44106195	CTATACTACTTTTTA[C/T]AAAAGGGCAAACTGG	5822
rs2516521	snp	C/T	0.481009	0.0955756	intron-variant	PWP2	GRCh38.p7	21:44108015	AATAAGAGGGGGCCG[C/T]GGAGCCGGCCTGGGG	5822
rs2516524	snp	A/G	0	0	utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B	TRAPPC10, PWP2	GRCh38.p7	21:44106018	CAGCACAGCCTAGGA[A/G]GGTCAGATCCTGTAT	5822
rs2776368	snp	C/T	0.489024	0.0732638	intron-variant	PWP2	GRCh38.p7	21:44112191	taaaatgctatcaaa[C/T]agtatcacatgctac	5822
rs2776369	snp	C/G	0	0	intron-variant	PWP2	GRCh38.p7	21:44114926	TGGGTGGCTGTGGTC[C/G]AGTCTTTGCGGCTCT	5822
rs2776371	snp	C/G			intron-variant	PWP2	GRCh38.p7	21:44123210	TGGGTGGCCTTGGGG[C/G]CTGGACCTGTGTCCC	5822
rs2838489	snp	C/G	0.482609	0.0916147	intron-variant	PWP2	GRCh38.p7	21:44128796	CCACCCCGTGGTTGA[C/G]CAGCTTGGGAAATGG	5822
rs2838490	snp	C/T	0.485799	0.0830599	intron-variant	PWP2	GRCh38.p7	21:44128915	TCTTGGAGGGATTGC[C/T]GCATTCGTAGGACCA	5822
rs2850152	snp	A/T	0.5	0	downstream-variant-500B, upstream-variant-2KB	TRAPPC10, PWP2	GRCh38.p7	21:44106690	GGAAACATTCGGATT[A/T]TTTTTTTTTTTTTTT	5822
rs2850153	snp	A/G	0.482979	0.0906686	intron-variant	PWP2	GRCh38.p7	21:44107579	GCTGTCTGCGCGCCC[A/G]TGGCCTCGGGGACGC	5822
rs2850154	snp	G/T	0.400504	0.199621	intron-variant	PWP2	GRCh38.p7	21:44112648	ACACAGCTCGGCTGC[G/T]TATGGGGAAGCTGGA	5822
rs2850155	snp	A/G	0.491577	0.0643472	intron-variant	PWP2	GRCh38.p7	21:44116329	AGATGCCGGGAGAGC[A/G]TTTGGCAAGGGTGGA	5822
rs2850156	snp	C/T	0.488965	0.0734569	intron-variant	PWP2	GRCh38.p7	21:44119148	CCCTTGCTCAGGGGT[C/T]GGGGGTCATAGCCTG	5822
rs2850157	snp	C/T	0.404605	0.196462	intron-variant	PWP2	GRCh38.p7	21:44120326	GTTGGGGTCTGCCCC[C/T]GCCCCTCCTGTCCTG	5822
rs2850158	snp	A/G	0	0	intron-variant	PWP2	GRCh38.p7	21:44123251	AACCTGTTCAGCAGA[A/G]GGTCTTCCTCCAGAA	5822
rs2850159	snp	A/G	0	0	intron-variant	PWP2	GRCh38.p7	21:44123267	GGTCTTCCTCCAGAA[A/G]GAAGTAGCGACCCTG	5822
rs2855650	snp	C/T	0.499759	0.0109798	intron-variant	PWP2	GRCh38.p7	21:44113373	cctgacctcgtgatc[C/T]gcccgccttggcctc	5822
rs2855651	snp	C/T	0.483126	0.0902898	intron-variant	PWP2	GRCh38.p7	21:44114933	CTGTGGTCCAGTCTT[C/T]GCGGCTCTGAAGTGT	5822
rs2855652	snp	C/G	0.383877	0.211225	intron-variant	PWP2	GRCh38.p7	21:44119359	GGTGGGCCTGAGCCG[C/G]GTACCCCAGCTTCCC	5822
rs2855653	snp	A/G	0.381308	0.21274	intron-variant	PWP2	GRCh38.p7	21:44120262	GGGCAAGCATCTTAG[A/G]TGGGGCGGCATGGGG	5822
rs2855654	snp	A/G	0.00438332	0.0466095	intron-variant	PWP2	GRCh38.p7	21:44113153	tttgtttgttttgag[A/G]cagagtcttgccctg	5822
rs3831654	in-del	-/GAGG/GAGT			intron-variant	PWP2	GRCh38.p7	21:44117109	TCAGTGCCCGTGAGT[-/GAGG/GAGT]CCGTGCCCGTCAGTG	5822
rs3948892	snp	A/G	0.0142736	0.0832652	intron-variant	PWP2	GRCh38.p7	21:44125942	TGGGGTCAAAGAGCA[A/G]GGGTAGGAGACGAGG	5822
rs4819373	snp	A/C	0.489024	0.0732638	intron-variant	PWP2	GRCh38.p7	21:44111831	ctcctgcctcgggcc[A/C]ccctaccaagtagct	5822
rs4819375	snp	C/T	0.227959	0.249026	intron-variant	PWP2	GRCh38.p7	21:44119767	GAGGGTCTGTGGTGC[C/T]GGCAGCCGGCATCCA	5822
rs5844173	in-del	-/G	0.489142	0.0728777	intron-variant	PWP2	GRCh38.p7	21:44118632	CTGAAGTGAATTGTT[-/G]GAGTCTGGTGAGTGG	5822
rs7280581	snp	C/T	0.482905	0.0908579	intron-variant	PWP2	GRCh38.p7	21:44129106	GCCTAGGACAGGGCC[C/T]GGCCCTCCGCAGTGC	5822
rs7282324	snp	A/G	0.356383	0.226236	intron-variant	PWP2	GRCh38.p7	21:44124905	GGCCGTGAAGCCAGC[A/G]CCTGCCTCAGCTGTG	5822
rs8127929	snp	C/T	0.0107246	0.0724382	intron-variant	PWP2	GRCh38.p7	21:44112606	CACGCTAGTAGACTA[C/T]GCCGTACTGTTTACA	5822
rs8130647	snp	A/G	0.481396	0.0946345	intron-variant	PWP2	GRCh38.p7	21:44112094	caacaaaggatttag[A/G]atatgacatcaactt	5822
rs9284512	snp	A/G	0.235564	0.249583	upstream-variant-2KB, downstream-variant-500B	C21orf33, PWP2	GRCh38.p7	21:44131632	CCCAGCCTGTCCCTC[A/G]CCAGCGGTGTGGCCC	5822
rs9306175	snp	C/T	0.25634	0.24992	utr-variant-3-prime	PWP2	GRCh38.p7	21:44130994	ACCTGGCCCCAGGAG[C/T]GGGGCCGTGTGAACG	5822
rs9978109	snp	A/C	0.115245	0.210632	synonymous-codon, downstream-variant-500B	PWP2	GRCh38.p7	21:44128032	CACCAGCGTCACCCC[A/C]GGGAGGGTGCGCGAG	5822
rs9980021	snp	C/G	0.153	0.230415	intron-variant	PWP2	GRCh38.p7	21:44119009	TCCCCTCCCCCAGCT[C/G]TCTGCCATGGGGTGC	5822
rs11089111	snp	A/G	0.489024	0.0732638	intron-variant	PWP2	GRCh38.p7	21:44110216	tgaaggaaattaaaa[A/G]tgctactccagtgaa	5822
rs11459330	in-del	-/G	0	0	intron-variant	PWP2	GRCh38.p7	21:44123237	CCCAGGAGCTCAGAA[-/G]CCTGTTCAGCAGAAG	5822
rs11550375	snp	C/T			synonymous-codon	PWP2	GRCh38.p7	21:44120712	GAGCGGTGAGATCGT[C/T]TCTGCAGGGGCGCAG	5822
rs11550376	snp	A/G	0.307096	0.243393	utr-variant-5-prime	PWP2	GRCh38.p7	21:44107410	CGGCACACGTGCGAC[A/G]GCCGTGATGAAGTTC	5822
rs11700553	snp	C/T			intron-variant	PWP2	GRCh38.p7	21:44112462	gaatgcttgtgcaca[C/T]tgatagactacagca	5822
rs11700919	snp	A/T	0.489083	0.0730708	intron-variant	PWP2	GRCh38.p7	21:44111254	acccatgagctccaa[A/T]ggagacgcataagga	5822
rs11701349	snp	A/C			intron-variant	PWP2	GRCh38.p7	21:44113874	TGATGTGGGCGGGTA[A/C]TGAGGGGACCAGTGA	5822
rs11908887	snp	A/C	0.067446	0.170804	utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B	TRAPPC10, PWP2	GRCh38.p7	21:44106271	CCTACCTGGTTTTTA[A/C]ATTTTATTTTTCATG	5822
rs11910166	snp	A/G	0.444444	0.157135	intron-variant	PWP2	GRCh38.p7	21:44109522	GCCCTGCTGCCACTG[A/G]GCCTCACCAGTCGGA	5822
rs17004631	snp	A/G	0.101658	0.201233	intron-variant	PWP2	GRCh38.p7	21:44126398	TCTGCTGCACAGCAC[A/G]CGGAGCATTCTGGCG	5822
rs17264579	snp	A/G	0.00795532	0.062565	intron-variant	PWP2	GRCh38.p7	21:44129259	AGCCATGTGAGGGAT[A/G]TCACCCTCTGTTGCC	5822
rs17856422	snp	A/T	0.0310059	0.120588	missense	PWP2	GRCh38.p7	21:44122191	GCTCTGGCTGTGACT[A/T]TTCGCCCTGATGGTG	5822
rs34215161	in-del	-/T			intron-variant, utr-variant-3-prime	PWP2	GRCh38.p7	21:44127757	ATCCATTCATTCCTT[-/T]CCCAGGGGAGTAGTG	5822
rs34455520	in-del	-/A			intron-variant	PWP2	GRCh38.p7	21:44118244	CACAGAGAACGAAAA[-/A]TACTATGCTCATAAA	5822
rs34550932	in-del	-/C			intron-variant	PWP2	GRCh38.p7	21:44126507	CGCCAGCCAGAAACC[-/C]TGAGTGCTTCCATAT	5822
rs34648825	in-del	-/A			intron-variant	PWP2	GRCh38.p7	21:44115416	ATGTCCCTTTGCCAA[-/A]GTTCCCTAGCCTGAT	5822
rs34880744	snp	C/T	0.00635571	0.056013	missense	PWP2	GRCh38.p7	21:44122260	CCGTCTGCACCGCGT[C/T]CTCAGGGTCCCAGAA	5822
rs35001460	snp	C/T	0.00316396	0.0396481	missense	PWP2	GRCh38.p7	21:44115313	GGTTGTCCCAGCGCT[C/T]GGCTCCGAACACCCA	5822
rs35040592	in-del	-/C	0.239037	0.24976	intron-variant	PWP2	GRCh38.p7	21:44114998	TTCACCTGTTTGTCC[-/C]AGAAACTGGGAATGC	5822
rs35267054	in-del	-/G			intron-variant	PWP2	GRCh38.p7	21:44123349	TGTGGAACTGCTGGG[-/G]TGCTGGTGGTTCTGT	5822
rs35292737	in-del	-/G			intron-variant	PWP2	GRCh38.p7	21:44120817	TGGGGCTCAGGAGGG[-/G]CCCTCCTGTCTCCTG	5822
rs35370163	in-del	-/G	0	0	intron-variant	PWP2	GRCh38.p7	21:44116602	CCGCGTCTGGGCTGT[-/G]GGGGGAGGCTGGTCA	5822
rs35798279	in-del	-/T	0	0	utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B	TRAPPC10, PWP2	GRCh38.p7	21:44106025	CCTAGGAAGGTCAGA[-/T]TCCTGTATTAATTAC	5822
rs35820620	in-del	-/C			intron-variant	PWP2	GRCh38.p7	21:44125686	TGGGGGAAAGTGTCC[-/C]TTGGCATTTTCACAA	5822
rs57123681	snp	A/G	0.00279162	0.0372561	intron-variant	PWP2	GRCh38.p7	21:44125301	GGGTTGGGAACCACT[A/G]CTGTGGATGACCCTG	5822
rs57855582	snp	A/G	0.230896	0.249269	intron-variant	PWP2	GRCh38.p7	21:44116856	CTGGGTGGGGAAGGC[A/G]CCCACACAAGGCCCT	5822
rs58016984	in-del	-/A			intron-variant	PWP2	GRCh38.p7	21:44108325	CAAGGTGGCAAAAAA[-/A]TGTGCCTTGGAGCCT	5822
rs58023015	snp	C/T	0.067446	0.170804	utr-variant-3-prime	PWP2	GRCh38.p7	21:44131151	CGTGAGGATGAAGTC[C/T]ACACTTCAGATTAAA	5822
rs58031932	snp	C/G	0.000798403	0.0199641	intron-variant	PWP2	GRCh38.p7	21:44122423	GCTCCTGCAGCTTCT[C/G]CATTTTTGGCCTTGT	5822
rs58611881	snp	A/G	0.00318978	0.0398085	intron-variant	PWP2	GRCh38.p7	21:44113907	AGGACTCAGGGCTGT[A/G]TGGGTCTGAAATGAT	5822
rs58714660	snp	A/G			intron-variant	PWP2	GRCh38.p7	21:44125285	CATGGGCCAGTACCA[A/G]GGGTTGGGAACCACT	5822
rs58734935	snp	C/T	0.000399281	0.0141238	intron-variant	PWP2	GRCh38.p7	21:44123963	ACACTGTTCCTTGAG[C/T]CACTTGTTCCTTTTG	5822
rs58771964	snp	C/T	0.000399281	0.0141238	intron-variant	PWP2	GRCh38.p7	21:44125524	CCTCAGCACAGCCCT[C/T]GGCTCAGGTCCCACT	5822
rs58851899	snp	C/T	0.000118776	0.00770544	missense	PWP2	GRCh38.p7	21:44113839	GCCTCGCTATCATCG[C/T]CGATGAAGGTACTTG	5822
rs58898739	in-del	-/A	0.412082	0.190341	intron-variant, downstream-variant-500B	PWP2	GRCh38.p7	21:44127870	TAAAAAAAAAAAAAA[-/A]GAAAAAAAATGTTGG	5822
rs59011068	snp	C/T	0.0314385	0.121371	intron-variant	PWP2	GRCh38.p7	21:44109991	CTCCCTATTCCCTGA[C/T]ACAAACAATGCTGAA	5822
rs59478103	in-del	-/T			downstream-variant-500B, upstream-variant-2KB	TRAPPC10, PWP2	GRCh38.p7	21:44106715	TTTTTTTTTTTTTTT[-/T]CTCTGAGACAGTCAT	5822
rs59487656	snp	A/G	0.0244538	0.107838	intron-variant	PWP2	GRCh38.p7	21:44126346	CCTCCCTGCCCTGGC[A/G]GGACCCGTCCATTTG	5822

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