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
rs11400	snp	C/T	0	0	synonymous-codon	MYCBP2	GRCh38.p7	13:77097740	TGAGGATGGGAAAAC[C/T]GAGACCACTTTTGAA	23077
rs383659	snp	G/T	0.188631	0.242351	intron-variant	MYCBP2	GRCh38.p7	13:77063964	TTCTGAGGATTAACC[G/T]AAGCAATTTTTACCA	23077
rs445080	snp	C/T	0.11228	0.208646	intron-variant	MYCBP2	GRCh38.p7	13:77046882	GGCACCAATCTGCAG[C/T]GTGATTTGGAGCAGG	23077
rs624575	snp	C/T	0.355525	0.226637	intron-variant	MYCBP2	GRCh38.p7	13:77048683	AATACCATCTACTCG[C/T]AGATTGTAAAAATGG	23077
rs670513	snp	A/T	0.354881	0.226936	intron-variant	MYCBP2	GRCh38.p7	13:77050023	CTCTTTTTTTTTTTT[A/T]AACTGATGCGTAATA	23077
rs687532	snp	C/G	0.340559	0.233022	intron-variant	MYCBP2	GRCh38.p7	13:77046925	GGGTGGGGGAGAGTG[C/G]GCAGGATGGGGACAC	23077
rs696779	snp	G/T	0.0146672	0.084371	intron-variant	MYCBP2	GRCh38.p7	13:77067440	CTAATATCTAAAAAG[G/T]TCATGTATAtaataa	23077
rs696780	snp	A/G	0.205723	0.246048	intron-variant	MYCBP2	GRCh38.p7	13:77067114	AACACAGAACCCAAA[A/G]TCATATAGGAAGATA	23077
rs700359	snp	A/G	0.449726	0.150364	intron-variant	MYCBP2	GRCh38.p7	13:77069016	AAACAAGTAAAGCTA[A/G]GGGAGCCACAATAAA	23077
rs727839	snp	C/T	0.347253	0.230308	intron-variant	MYCBP2	GRCh38.p7	13:77219237	GACTCATTGGAGGAG[C/T]AGGTTTCAAGCGTGG	23077
rs851507	snp	C/T	0.0107246	0.0724382	intron-variant	MYCBP2	GRCh38.p7	13:77058138	agccactgcgcccgg[C/T]cTCAATCAATGTTTA	23077
rs851508	snp	A/G	0.202035	0.245356	intron-variant	MYCBP2	GRCh38.p7	13:77059058	GCATCACCAAAATGC[A/G]GATTTTTTTTTTTTT	23077
rs851509	snp	A/G	0.0240643	0.107019	intron-variant	MYCBP2	GRCh38.p7	13:77069398	gaggccgaggcgggc[A/G]gatcatgagatcagg	23077
rs851512	snp	G/T	0.0103295	0.0711199	intron-variant	MYCBP2	GRCh38.p7	13:77049192	CATGCTTGGAGGGAG[G/T]GGGTGATGTGCTGGA	23077
rs851513	snp	C/G	0.0103295	0.0711199	intron-variant	MYCBP2	GRCh38.p7	13:77049979	TCCTGAAGATCTTTC[C/G]AAATCAGCACACAGA	23077
rs851514	snp	C/T	0.0103295	0.0711199	intron-variant	MYCBP2	GRCh38.p7	13:77052998	cagaaattagccagg[C/T]gtggtggtgaggacc	23077
rs861142	snp	A/G	0.00953873	0.0683987	intron-variant	MYCBP2	GRCh38.p7	13:77055066	aagaggtcacccaag[A/G]taaggaagtatttat	23077
rs864850	snp	C/T	0.0551013	0.156571	intron-variant	MYCBP2	GRCh38.p7	13:77057938	CGTCTCCTGGCTTCA[C/T]GCCATTCTCCTGACT	23077
rs866451	snp	C/T	0.00953873	0.0683987	intron-variant	MYCBP2	GRCh38.p7	13:77063473	ctgagacaggagaat[C/T]gcttgtacctgcagg	23077
rs927852	snp	C/T	0.489434	0.0719116	intron-variant	MYCBP2	GRCh38.p7	13:77097196	TGGCCATCATAATAT[C/T]AGAATTTATCTGTTT	23077
rs927967	snp	G/T	0.4944	0.0526182	intron-variant, upstream-variant-2KB	MYCBP2	GRCh38.p7	13:77228036	ATATATTTTAATTCT[G/T]CCACTGCTGCTGATA	23077
rs957259	snp	A/G	0.421051	0.182323	intron-variant	MYCBP2	GRCh38.p7	13:77091129	TATTAGAAAATAGAT[A/G]ATTTTACCAAGGGAC	23077
rs959810	snp	A/G	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77091186	ATGTACATAAGCTTA[A/G]AGAAGTGGTGAGTAA	23077
rs961590	snp	G/T	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77281786	TTATGATCACACTTA[G/T]TCATGAAATAATAAA	23077
rs1041242	snp	A/G	0.200801	0.245111	intron-variant	MYCBP2	GRCh38.p7	13:77194037	CTATGAATATCAAAT[A/G]CTTGAGAAATTAAAT	23077
rs1178626	snp	C/T	0.0170251	0.090679	intron-variant	MYCBP2	GRCh38.p7	13:77069652	acgaggtcaggagat[C/T]gagaccatcctggct	23077
rs1178627	snp	C/T	0.354881	0.226936	intron-variant	MYCBP2	GRCh38.p7	13:77072954	tttcatcttgtttac[C/T]tctttcatcatttat	23077
rs1178628	snp	A/G	0.109814	0.206997	intron-variant, upstream-variant-2KB	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77074985	aggccaatgctggca[A/G]actgcttgagcccag	23077
rs1340530	snp	A/G	0.0726307	0.176182	intron-variant	MYCBP2	GRCh38.p7	13:77128130	TCTCTGTGTATTCAT[A/G]TAGGTTTGCATATAT	23077
rs1340531	snp	G/T	0.224116	0.248656	intron-variant	MYCBP2	GRCh38.p7	13:77056859	CAGGTTCCACATGAA[G/T]GAGAAGGGAAGAAAC	23077
rs1473756	snp	C/T	0.0023933	0.0345097	intron-variant	MYCBP2	GRCh38.p7	13:77097146	TAATATTTTTTAAAA[C/T]ATGCTACATGAAAGT	23077
rs1538849	snp	G/T	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77056101	ACGCTCTGTGTTTGg[G/T]gtgtgtgtgtgtgtg	23077
rs1571296	snp	G/T	0.0633504	0.166319	intron-variant	MYCBP2	GRCh38.p7	13:77271082	AAAAGTATGATTAAG[G/T]AGTGAGAATATAAAA	23077
rs1633532	snp	G/T	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77071115	GTGGTCTTAAATTAA[G/T]CTATCGGAACACCAA	23077
rs1633533	snp	A/G	0.0138799	0.0821421	intron-variant	MYCBP2	GRCh38.p7	13:77071275	TGTGTGcacacgcac[A/G]cacacacacacacac	23077
rs1770574	snp	A/G			intron-variant	MYCBP2	GRCh38.p7	13:77108910	gggtttcactgtgtt[A/G]gccaggatggtcgac	23077
rs1770575	snp	A/C			intron-variant	MYCBP2	GRCh38.p7	13:77108917	actgtgttagccagg[A/C]tggtcgacctcgtga	23077
rs1773244	snp	A/G	0.0387552	0.1337	intron-variant	MYCBP2	GRCh38.p7	13:77071273	CGTGTGTGcacacgc[A/G]cgcacacacacacac	23077
rs1934738	snp	C/G	0.0174175	0.0916809	intron-variant	MYCBP2	GRCh38.p7	13:77089647	CCAGATCATGTAACT[C/G]TTTTTTTTTTTTTTT	23077
rs1969954	snp	C/T	0.44638	0.154709	intron-variant	MYCBP2	GRCh38.p7	13:77193854	TACGGAATACCTAGT[C/T]TGCTGGTGTTCTAGT	23077
rs2025907	snp	A/G	0.495407	0.0477027	intron-variant	MYCBP2	GRCh38.p7	13:77242639	TCTATTTTCTTACTC[A/G]TTTATGCTCATTATC	23077
rs2027406	snp	A/G	0.419456	0.183806	intron-variant	MYCBP2	GRCh38.p7	13:77130183	TGGTTCAAAATAACC[A/G]TTTATCATAATATTT	23077
rs2031804	snp	A/T	0.495291	0.0482933	intron-variant	MYCBP2	GRCh38.p7	13:77241241	GGAAATAAAGGAACA[A/T]TGAATCGTGCATTGA	23077
rs2031805	snp	A/G	0.0629771	0.165899	intron-variant	MYCBP2	GRCh38.p7	13:77213464	ttgagacagagcctc[A/G]ctctgtcatccaggc	23077
rs2039872	snp	A/G	0.192401	0.243274	intron-variant	MYCBP2	GRCh38.p7	13:77109257	aatagtctcaagatg[A/G]aactgctccacctca	23077
rs2039873	snp	A/G	0.0414363	0.137845	intron-variant	MYCBP2	GRCh38.p7	13:77110915	TTAGGCCCCTAGAAC[A/G]CTTGAAATTATGCCA	23077
rs2073840	snp	C/T	0.419456	0.183806	intron-variant	MYCBP2	GRCh38.p7	13:77065456	TTGTCCTTCTCAGGC[C/T]GCCCTCCTAGAAATA	23077
rs2153504	snp	C/T	0.0614824	0.164198	intron-variant	MYCBP2	GRCh38.p7	13:77127662	CTATTTAATACAATT[C/T]TATCTTGCATAATGT	23077
rs2153506	snp	C/T	0.0614824	0.164198	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77077603	AGAAACTAAGGTTAA[C/T]ACAGGTTAAGGGATT	23077
rs2153507	snp	C/T	0.0170251	0.090679	intron-variant	MYCBP2	GRCh38.p7	13:77091740	CTTTTTTTTTTTAAA[C/T]AGAAGGGGTCTTGCT	23077
rs2153508	snp	C/T			missense	MYCBP2	GRCh38.p7	13:77096455	CAATGCTATTGTAAC[C/T]TTGTCCACCAGCATA	23077
rs2185468	snp	A/C	0.352721	0.227922	intron-variant	MYCBP2	GRCh38.p7	13:77092041	TTCTGACGAGTAATC[A/C]ACACAGTTGGGGAGG	23077
rs2274547	snp	A/G	0.323861	0.23884	synonymous-codon	MYCBP2	GRCh38.p7	13:77164529	CTAATTCTTTTTCCA[A/G]TTGGATGACTCCCTA	23077
rs2274548	snp	A/G	0.352721	0.227922	intron-variant	MYCBP2	GRCh38.p7	13:77165526	TACATAACTTAAATA[A/G]ACTTGCGGCGGGGAG	23077
rs2274549	snp	C/T	0.158302	0.232576	intron-variant	MYCBP2	GRCh38.p7	13:77165532	ACTTAAATAGACTTG[C/T]GGCGGGGAGCGTTCC	23077
rs2275561	snp	A/G	0.113075	0.209169	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081413	AGAGCCGTAAATCAC[A/G]TTTGCTTTCTTACCC	23077
rs2275562	snp	G/T	0.0422008	0.138995	intron-variant	MYCBP2	GRCh38.p7	13:77126656	ATCTTTAGTTATGTG[G/T]TTTTTTTATATTGAC	23077
rs2277418	snp	A/G	0.186737	0.241863	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77078946	GCTTCAGAACTTACA[A/G]TGGTTTCTCATGACC	23077
rs2285383	snp	G/T	0.0410537	0.137264	intron-variant	MYCBP2	GRCh38.p7	13:77051549	AAGTTTCACTGCACG[G/T]TTAAGAAACTAAGAA	23077
rs2285384	snp	C/T	0.0425829	0.139564	intron-variant	MYCBP2	GRCh38.p7	13:77051665	ATAATATATATGAAA[C/T]AATGTGAAAAATTAT	23077
rs2285385	snp	A/G	0.124144	0.21601	intron-variant	MYCBP2	GRCh38.p7	13:77052275	GCAATCATGGCTCCC[A/G]ACAGCCTCAACCTCT	23077
rs2285386	snp	C/T	0.187999	0.24219	synonymous-codon	MYCBP2	GRCh38.p7	13:77058335	ACAGGGCAGACAGTG[C/T]TCTTCGTTTTTAACA	23077
rs2285387	snp	A/G	0.49655	0.04139	intron-variant	MYCBP2	GRCh38.p7	13:77058910	GAATCGCTTGAACCC[A/G]GGAGGCGGAGGTTGC	23077
rs2285388	snp	C/T	0.0618563	0.164627	intron-variant	MYCBP2	GRCh38.p7	13:77061110	AGTTTAATCAGTTGG[C/T]ACGGTTTAATCTTTT	23077
rs2285389	snp	A/G	0.493154	0.0581045	intron-variant	MYCBP2	GRCh38.p7	13:77061392	TCAATAATAATAATG[A/G]CTTTCATTTAAGCAC	23077
rs2296854	snp	A/G	0.0325976	0.123435	intron-variant	MYCBP2	GRCh38.p7	13:77161652	TCCTCCGCACCCTTG[A/G]CACTTGATTTGTTTT	23077
rs2296855	snp	A/G	0.4941	0.0539917	intron-variant	MYCBP2	GRCh38.p7	13:77162184	CAAGAAGCATCCATG[A/G]GTGATTTGCCAAAGA	23077
rs2301580	snp	C/T	0.0845197	0.187393	intron-variant	MYCBP2	GRCh38.p7	13:77055795	ATGAACACTCTTTAG[C/T]AGAATCATTTATTAA	23077
rs2301581	snp	A/G	0.0724097	0.175959	intron-variant	MYCBP2	GRCh38.p7	13:77055819	TTATTAACCAACTCA[A/G]CAAACACTTAGCATG	23077
rs2328998	snp	G/T	0.125182	0.216612	intron-variant	MYCBP2	GRCh38.p7	13:77053409	TGTCCGGATTGGGAA[G/T]AAACAAACTGAGTCA	23077
rs2328999	snp	A/G	0.353587	0.22753	intron-variant	MYCBP2	GRCh38.p7	13:77112373	aaatatatattatat[A/G]ttatataaataaaat	23077
rs2329026	snp	C/T	0.0490535	0.14873	intron-variant	MYCBP2	GRCh38.p7	13:77154261	CATGTCAGATTTATC[C/T]AATTTAGAAACTTTC	23077
rs2329027	snp	A/G	0.494358	0.0528145	intron-variant	MYCBP2	GRCh38.p7	13:77276862	TTGGGACCAGTCTGG[A/G]CAACTTAGACCCCTA	23077
rs2329028	snp	A/C	0.450231	0.149691	intron-variant	MYCBP2	GRCh38.p7	13:77276667	TCTACCAAAAAAAAA[A/C]CCCCCAAAAAATCCC	23077
rs2329029	snp	A/C	0.445592	0.155704	intron-variant	MYCBP2	GRCh38.p7	13:77208161	tttaaagaggaaaag[A/C]gagcaggaggagaaa	23077
rs2428006	snp	C/T	0.0629771	0.165899	intron-variant	MYCBP2	GRCh38.p7	13:77052347	aggatcataggtgca[C/T]gccaccacacccggc	23077
rs2487755	snp	C/T	0.0622301	0.165053	intron-variant	MYCBP2	GRCh38.p7	13:77052510	AATCCATTTGAGAGT[C/T]GAAATAGCTTTAggc	23077
rs3038650	in-del	-/TT	0.405603	0.195673	intron-variant	MYCBP2	GRCh38.p7	13:77234844	AAATGGTAATATAAC[-/TT]AATATTATTACCTTA	23077
rs3742103	snp	C/T	0.149379	0.228857	intron-variant	MYCBP2	GRCh38.p7	13:77166574	GGTCAACAGGCAAAG[C/T]GACATGAATACAGAT	23077
rs3752990	snp	A/G	1.64846e-05	0.0028709	synonymous-codon	MYCBP2	GRCh38.p7	13:77166447	ATATCCTGAATTCTG[A/G]ACAGTTCTGACAGGA	23077
rs3752991	snp	A/C	0.0551013	0.156571	intron-variant	MYCBP2	GRCh38.p7	13:77212319	TTATAAATATTTGGT[A/C]CAAATTCTTACATAT	23077
rs3753040	snp	A/C	0.00566454	0.0529168	intron-variant	MYCBP2	GRCh38.p7	13:77095629	AAAAATCAAACTAAT[A/C]TTTTCTGACTTACAT	23077
rs3825499	snp	G/T	0.15698	0.23205	intron-variant	MYCBP2	GRCh38.p7	13:77224761	CACACTTAAAAATTC[G/T]TATAAATGCCATTTA	23077
rs3832881	in-del	-/A	0.122259	0.2149	intron-variant	MYCBP2	GRCh38.p7	13:77166314	CACATAAAACAGAAG[-/A]AAAAAAAAACTTACC	23077
rs3837533	in-del	-/A	0.138546	0.223781	intron-variant	MYCBP2	GRCh38.p7	13:77048861	ACCACTGAGTTCTCT[-/A]AAAGTGTTTCATTGT	23077
rs3841487	in-del	-/AT	0.0588605	0.161139	intron-variant	MYCBP2	GRCh38.p7	13:77068974	AGTTAATTCTCCATC[-/AT]ATGTCATTCTCTTAA	23077
rs3861128	snp	C/T	0.491263	0.0655142	intron-variant	MYCBP2	GRCh38.p7	13:77158198	ATTTCTCCGTAAAGG[C/T]CTATCTGAAAGTATC	23077
rs3889340	snp	C/T	0.0364509	0.129988	intron-variant	MYCBP2	GRCh38.p7	13:77184844	TGGTTCTTTTCCTCT[C/T]TCCCTCTCTCAGAAT	23077
rs4052542	snp	A/G	0.0629771	0.165899	intron-variant	MYCBP2	GRCh38.p7	13:77199742	cagttaggctgctgg[A/G]gggtcaggggtcagg	23077
rs4267189	snp	A/G	0.00517822	0.0506191	intron-variant	MYCBP2	GRCh38.p7	13:77197035	atgaagtgtagtgtc[A/G]tgggggacaagagaa	23077
rs4465498	snp	A/G	0.494187	0.0535994	intron-variant	MYCBP2	GRCh38.p7	13:77141726	CAGTGGGCAGGGATC[A/G]CGCCACTGCATTCCA	23077
rs4470045	snp	A/G	0.0170251	0.090679	intron-variant	MYCBP2, MYCBP2-AS1	GRCh38.p7	13:77081088	TTTGAGAGACCCTGG[A/G]AGAATTGATCAGCAG	23077
rs4489888	snp	C/T	0.4944	0.0526182	intron-variant	MYCBP2	GRCh38.p7	13:77093953	TTTCACGTTTTACAA[C/T]TTGATTCTTTCCTTT	23077
rs4594140	snp	C/T	0.0387552	0.1337	intron-variant	MYCBP2	GRCh38.p7	13:77210856	ACCTAGTATGCACCT[C/T]TGTAGTATTAGCATC	23077
rs4594141	snp	C/T	0.0372196	0.131242	intron-variant	MYCBP2	GRCh38.p7	13:77210931	TTCTCCAGGGTGACA[C/T]AGAAAGCAAGTTGTG	23077
rs4884059	snp	C/T	0.495213	0.048687	intron-variant	MYCBP2	GRCh38.p7	13:77199447	gatcaaactgcaagg[C/T]ggcagcgaggctggg	23077
rs4884060	snp	C/T	0.0441095	0.141807	intron-variant	MYCBP2	GRCh38.p7	13:77243655	TCATCCCTTAAACAA[C/T]GTCATATTGTCAGTT	23077
rs4884061	snp	A/T	0	0	intron-variant	MYCBP2	GRCh38.p7	13:77277445	AAAATCCTCAGCTTG[A/T]TTCAATGACCAGCAT	23077
rs4884062	snp	C/G	0.0107246	0.0724382	intron-variant	MYCBP2	GRCh38.p7	13:77277644	TAAACCAGCAGTGTA[C/G]TCCTCAAACCAGCAT	23077
rs4885442	snp	A/G	0.494442	0.0524218	intron-variant	MYCBP2	GRCh38.p7	13:77147013	CAGATTATGGAATAG[A/G]TCCCCAATGGAATGC	23077

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