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
rs12109	snp	G/T	0	0	missense, utr-variant-5-prime	MYLIP	GRCh38.p7	6:16129365	GCGGTGCTGATGGAG[G/T]TGGAGGTGGAGGCGA	29116
rs760632	snp	C/T	0.356383	0.226236	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128841	CACCAGCCGCCTCTG[C/T]CCGCTGGGCGACGCT	29116
rs760633	snp	C/G	0.442655	0.159323	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128734	CTCCAAGCTGCCACT[C/G]TTCTTCAAATATCTT	29116
rs909562	snp	C/T	0.390838	0.206555	intron-variant	MYLIP	GRCh38.p7	6:16130102	CTTCACAAGCGGTTT[C/T]CCAAACA	29116
rs1011616	snp	A/G	0.338523	0.233803	intron-variant	MYLIP	GRCh38.p7	6:16132178	TATTTGGTACTCCAA[A/G]CTTCTGAAGATTTAA	29116
rs1060901	snp	C/T	0.0486741	0.148216	synonymous-codon	MYLIP	GRCh38.p7	6:16145242	GTGCATGGTGTGCTG[C/T]GAGGAGGAGATCAAC	29116
rs1060913	snp	A/G	0.340108	0.233197	intron-variant	MYLIP	GRCh38.p7	6:16146509	TTCAACCTGTGAGAC[A/G]GCAAAGATCTCTACC	29116
rs1076632	snp	A/G	0.0770498	0.180522	intron-variant	MYLIP	GRCh38.p7	6:16129469	CCGAGGGGCCTCGCA[A/G]CGACGCCTGGCACTC	29116
rs2056937	snp	A/G	0.497182	0.037434	intron-variant	MYLIP	GRCh38.p7	6:16144383	TTAAAAAATCCTTCC[A/G]TACACAGTGACGACT	29116
rs2066905	snp	C/G	0.356169	0.226336	intron-variant	MYLIP	GRCh38.p7	6:16131066	TCAGGAAGTCAGTCA[C/G]TCGGGTAGGGTGGTT	29116
rs2072780	snp	A/G	0.373598	0.21731	intron-variant	MYLIP	GRCh38.p7	6:16144689	GACATTATGGCTTCC[A/G]TAAAGCAGTAAATAC	29116
rs2072781	snp	A/G	0.282632	0.247861	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147118	TAGGAAACTTACCTC[A/G]GGATACATTAAGGAG	29116
rs2072782	snp	G/T	0.00755907	0.0610114	intron-variant	MYLIP	GRCh38.p7	6:16146442	TGACATAGTATAAAC[G/T]GAAGGAAATTAATTA	29116
rs2072783	snp	C/T	0.283453	0.247752	intron-variant	MYLIP	GRCh38.p7	6:16143666	AAAAGAAAGCAGATC[C/T]AGAAGGAGTGATTCT	29116
rs2072784	snp	C/T	0.314057	0.241654	intron-variant	MYLIP	GRCh38.p7	6:16143633	ACCATGTGTGTGCCT[C/T]TGTGGGATCCCCATT	29116
rs2076017	snp	C/T	0.196771	0.244268	intron-variant	MYLIP	GRCh38.p7	6:16130328	CATGACCAATTGCAA[C/T]AGAGAAAAAAGGAGT	29116
rs2142674	snp	G/T	0.361263	0.223876	intron-variant	MYLIP	GRCh38.p7	6:16138434	AGAACTTCAGTGATG[G/T]CTCAATATTTATGGG	29116
rs2142675	snp	C/G	0.494442	0.0524218	intron-variant	MYLIP	GRCh38.p7	6:16138132	TTTCTCTGTCTTAAG[C/G]AAATGTCCATGAATA	29116
rs2205794	snp	C/T	0.123798	0.215808	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147945	AGCTAGTATTGCACC[C/T]GATAAGGTCATCTAG	29116
rs2205795	snp	A/C	0.340333	0.233109	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147827	CAAAAAGAACCAAAA[A/C]CCCTTCGAAACATAC	29116
rs2205796	snp	A/C	0.376791	0.215463	intron-variant	MYLIP	GRCh38.p7	6:16142766	TTGGAAGAATTATGG[A/C]AAGTCTCTAAAAATA	29116
rs2235215	snp	A/G	0.48546	0.0840147	intron-variant	MYLIP	GRCh38.p7	6:16130925	TTGGAAAATGCACTC[A/G]GACCAAGTAGGTAGC	29116
rs2237106	snp	A/G	0.287867	0.247116	intron-variant	MYLIP	GRCh38.p7	6:16133755	GTGGCTAAGTCGGGA[A/G]CAAAATATAGATTTT	29116
rs2237107	snp	C/G	0.301932	0.244547	intron-variant	MYLIP	GRCh38.p7	6:16133589	ATGATTATTATTTCA[C/G]ATCTACTTCCAGAAT	29116
rs2282813	snp	A/C	0.317933	0.240593	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140400	ATCCTGTTTAAGCCC[A/C]TCCTAGTTGTATACA	29116
rs2282814	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16139439	TTGCCACAAACGAAG[C/T]CTTCTTAGTTTAATT	29116
rs2327950	snp	C/T	0	0	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128323	TTTCTTTTCTTTTTT[C/T]TTTTTTTTTTTTTTT	29116
rs3071239	in-del	-/TTTT			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128342	ttttttttttttttt[-/TTTT]gagacagggtttttt	29116
rs3071241	in-del	-/T/TT			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128512	tttgttttttttttt[-/T/TT]gtatttttagtagag	29116
rs3216216	in-del	-/T	0.495368	0.0478996	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140356	CATTTACTAAAAGGT[-/T]ATGTCACACTTAAAA	29116
rs3757352	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128640	AAAGAAAACTGTTCT[C/G]GTccgggcatggtgg	29116
rs3757353	snp	C/T	0.373598	0.21731	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127642	GGTTTCGCAACACAG[C/T]GAAACCCCATCTCTA	29116
rs3757354	snp	A/G	0.440333	0.16209	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127176	AAGGATCTGTTAGTG[A/G]CCTTTATTTCCGAAC	29116
rs3765234	snp	A/C	0.178785	0.239642	utr-variant-5-prime	MYLIP	GRCh38.p7	6:16129267	GTGTGCGCGGGGCTG[A/C]CGCCTTGTCACTGGT	29116
rs4515393	snp	A/G	0.0463947	0.145069	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140997	ATTTAAATAGTTTTC[A/G]GAGAGAAGAAAGTCA	29116
rs4716047	snp	A/G	0.361894	0.223562	intron-variant	MYLIP	GRCh38.p7	6:16138027	TTTCTTAGTAACTGG[A/G]TAAAACTTAAAGAAG	29116
rs4716048	snp	C/G	0.487933	0.0767327	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140596	GGTATCCAAGCAAGG[C/G]GACAGAAAGAATGGC	29116
rs4716049	snp	A/T	0.486855	0.0799975	downstream-variant-500B, intron-variant	MYLIP	GRCh38.p7	6:16148512	GGAGATCACTTCACC[A/T]GGTTATTCTCTTATT	29116
rs4716050	snp	A/G	0.484138	0.0876334	downstream-variant-500B, intron-variant	MYLIP	GRCh38.p7	6:16148513	GAGATCACTTCACCA[A/G]GTTATTCTCTTATTT	29116
rs5874546	in-del	-/T			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128317	TTTCTTTTTCTTTTC[-/T]TTTTTTTTTTTTTTT	29116
rs6920309	snp	C/T	0.35207	0.228214	intron-variant	MYLIP	GRCh38.p7	6:16134016	CTTTCTGACCTCAGC[C/T]CCATCCTCAGCCCTC	29116
rs7738525	snp	A/G	0.486464	0.0811471	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16141371	ATTTTATGTTTTGTA[A/G]CCTTAATGTTACCGA	29116
rs7756075	snp	A/G	0.258565	0.249853	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16141385	AACCTTAATGTTACC[A/G]AACTTGTGTTAAATA	29116
rs7763395	snp	A/G	0.491263	0.0655142	intron-variant	MYLIP	GRCh38.p7	6:16142128	CATCAGGGCTACTGC[A/G]TATATTCATAGAGCT	29116
rs8180638	snp	C/T	0.382085	0.212258	intron-variant	MYLIP	GRCh38.p7	6:16134945	GGAAGGTTTTTAAAA[C/T]GACATGTAAAATTAA	29116
rs9297003	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16135805	attctatatagtgta[C/T]atatacagtatatat	29116
rs9297004	snp	C/G	0.029116	0.117091	intron-variant	MYLIP	GRCh38.p7	6:16135813	tagtgtatatataca[C/G]tatatattctatata	29116
rs9349995	snp	A/T	0.297128	0.245518	intron-variant	MYLIP	GRCh38.p7	6:16134371	GAAAAGTTGAGAGTA[A/T]CTAAAAGAAATCTCA	29116
rs9370867	snp	A/G	0.47729	0.104112	missense	MYLIP	GRCh38.p7	6:16145094	ACCTCGTTTCAAGAA[A/G]CAACCAGAGCCCTTC	29116
rs9396644	snp	C/T	0.0399052	0.1355	intron-variant	MYLIP	GRCh38.p7	6:16145537	CTCCAAATTATGCAG[C/T]GTTTTCAAGTTCTGA	29116
rs10602844	in-del	-/TATATA			intron-variant	MYLIP	GRCh38.p7	6:16135756	GTGTATACATATATC[-/TATATA]TATATATATATATAT	29116
rs11354447	in-del	-/A	0.493201	0.0579089	intron-variant	MYLIP	GRCh38.p7	6:16137887	TATATTCACTCCATT[-/A]AAAAAAAAATCTATA	29116
rs11394742	in-del	-/AA			intron-variant	MYLIP	GRCh38.p7	6:16131047	AAAAAAAAAAAAAAA[-/AA]GAAACCACCCTACCC	29116
rs11552211	snp	A/G			utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16148131	TAAATACCTCTTGGA[A/G]TAAAGGCTTATATGC	29116
rs11963978	snp	C/T	0.00597247	0.0543191	downstream-variant-500B, intron-variant	MYLIP	GRCh38.p7	6:16148328	ACATCACAGTTAGTA[C/T]CTACTTTCCTCCTAC	29116
rs11968699	snp	A/G	0.0150606	0.0854603	intron-variant	MYLIP	GRCh38.p7	6:16138327	CTACTTTACAAAAAA[A/G]AAAAGGAGGGGGCAA	29116
rs11969716	snp	A/G	0.00199481	0.0315187	intron-variant	MYLIP	GRCh38.p7	6:16142861	TCTTAGACGTTTTTT[A/G]TAGTAAGTTCGCTAA	29116
rs12202423	snp	G/T			utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147933	ATGTCGGGAGACCTA[G/T]ATGACCTTATCGGGT	29116
rs13192810	snp	A/T			intron-variant	MYLIP	GRCh38.p7	6:16129511	CTACTAGGGGCCGGG[A/T]GGCACTGCGGCGGCA	29116
rs13194722	snp	G/T			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128523	tttttgtatttttag[G/T]agagacgggggtttc	29116
rs13206355	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16129512	TACTAGGGGCCGGGA[A/G]GCACTGCGGCGGCAG	29116
rs13207341	snp	A/C			intron-variant	MYLIP	GRCh38.p7	6:16129499	CTGGCGCGCCCCCTA[A/C]TAGGGGCCGGGAGGC	29116
rs34308252	in-del	-/C			intron-variant	MYLIP	GRCh38.p7	6:16131903	TGAGTTCTTGGTACT[-/C]CCTGAAAATATCTTG	29116
rs34444721	snp	A/G	0.000723251	0.0190027	intron-variant, nc-transcript-variant	MYLIP, MIR4639	GRCh38.p7	6:16141594	GTCAGGTTATCCCCA[A/G]GCATAACCTCACTCT	29116
rs34627146	snp	A/G	0.0113489	0.0744692	synonymous-codon, intron-variant	MYLIP	GRCh38.p7	6:16143849	AGCGATAACAGAGAC[A/G]CACGCATTCTACAGG	29116
rs34659321	in-del	-/G			intron-variant	MYLIP	GRCh38.p7	6:16129836	CAGTCTCGGGCCCCA[-/G]GGGTTCTTGGCAGAC	29116
rs34983380	in-del	-/G			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127633	ATTTTGTGTAGAGAT[-/G]GGGGTTTCGCTGTGT	29116
rs35112615	in-del	-/A/AA			utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16146867	TAAAAAAAAAAAAAA[-/A/AA]GGAAGAAAAATAACA	29116
rs35212780	snp	A/C	0.027392	0.113779	synonymous-codon	MYLIP	GRCh38.p7	6:16143170	GCTCATTGGGGTTGG[A/C]CCTGAAGGAATCTCA	29116
rs35613901	in-del	-/G			intron-variant	MYLIP	GRCh38.p7	6:16134718	CACAAAATAGGCCCT[-/G]GGAAAGTAAAAACAG	29116
rs35729822	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16132736	ATGCATGAAACTATA[A/G]AACAAAAATATGTAT	29116
rs35731512	in-del	-/G			intron-variant	MYLIP	GRCh38.p7	6:16142603	TGAAGGCTCGACTGA[-/G]GGGTGGCCTCCATGC	29116
rs36160962	snp	C/T			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128288	AGTTTTCTTTTTCTC[C/T]TTTTTTTTTCTTTTT	29116
rs45542142	snp	A/G	0.0158469	0.0875917	intron-variant	MYLIP	GRCh38.p7	6:16144727	GTTAGAGAAACAGAG[A/G]TGTAATCACTGAGAA	29116
rs55828581	snp	A/G	0.0166325	0.0896639	intron-variant	MYLIP	GRCh38.p7	6:16139475	TTCAAGTCTTTCAGA[A/G]CGTAATTTCTTCTTT	29116
rs56215044	snp	A/C			intron-variant	MYLIP	GRCh38.p7	6:16135755	TGTGTATACATATAT[A/C]TATATATATATATAT	29116
rs57547267	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16135779	TATATATATATATAT[A/G]TATGCTATATATTCT	29116
rs61711295	in-del	-/AAG			intron-variant	MYLIP	GRCh38.p7	6:16143294	ATAGAAAATAGGAAG[-/AAG]GGATTTACTCGACAG	29116
rs62387664	snp	A/G	0.5	0	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16146883	AAAAAAAAAAAAAAG[A/G]AAGAAAAATAACACA	29116
rs71716432	in-del	-/T/TT	0.280785	0.248097	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128501	CGCCTGGCTATTTTG[-/T/TT]TTTTTTTTTTTGTAT	29116
rs72833422	snp	G/T	0.0146672	0.084371	intron-variant	MYLIP	GRCh38.p7	6:16133501	GCATATTTCAGAGAT[G/T]GAGACAGCAGGTTAT	29116
rs72833427	snp	A/C/T	3.29453e-05	0.00405854	synonymous-codon	MYLIP	GRCh38.p7	6:16145071	TCTGTACAATGCTGG[A/C/T]GTTGTGGACCTCGTT	29116
rs73377721	snp	C/T	0.0107246	0.0724382	intron-variant	MYLIP	GRCh38.p7	6:16131556	GAGACTTCAATCTTA[C/T]AGTGGCATATCAAAA	29116
rs73724995	snp	A/G	0.0146672	0.084371	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147622	CAACTGAGGGTAGTT[A/G]ACTCATCACTTCTCC	29116
rs74484260	snp	A/G	0.0150606	0.0854603	intron-variant	MYLIP	GRCh38.p7	6:16144791	TTCATACATGCAGAC[A/G]AGACTATGAAACATC	29116
rs74519493	snp	A/G	0.00755907	0.0610114	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140852	AGAAATGACAAGTTT[A/G]TACTAGAAACAAGCA	29116
rs74641795	snp	C/T	0.0287284	0.116357	downstream-variant-500B, intron-variant	MYLIP	GRCh38.p7	6:16148453	ATAGTCTTTTTTTTT[C/T]TTTTTCAAGAAAACT	29116
rs74708826	snp	A/G	0.5	0	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16146881	TTAAAAAAAAAAAAA[A/G]GGAAGAAAAATAACA	29116
rs75833122	snp	G/T	0.0162398	0.0886349	intron-variant	MYLIP	GRCh38.p7	6:16146435	AAAAATGTAATTAAT[G/T]TCCTTCAGTTTATAC	29116
rs76272508	snp	A/G	0.0189856	0.0955633	intron-variant	MYLIP	GRCh38.p7	6:16144003	GAACATTTTGTTTCC[A/G]TAGTAGCAGTGGAGT	29116
rs76482829	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140073	CTTGCTCATGTTCCT[C/T]TACCTGGAATGTCAG	29116
rs76502194	snp	G/T	0.5	0	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128513	TTTGTTTTTTTTTTT[G/T]TATTTTTAGTAGAGA	29116
rs76514709	snp	A/G	0.00159617	0.0282053	intron-variant	MYLIP	GRCh38.p7	6:16136385	CACAGATTTTTTGAG[A/G]TCCATCCATATTGTC	29116
rs76726799	snp	A/G	0	0	intron-variant	MYLIP	GRCh38.p7	6:16131032	GTGCTACCCCAGGAA[A/G]AAAAAAAAAAAAAAA	29116
rs77545634	snp	G/T	0	0	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128512	TTTTGTTTTTTTTTT[G/T]GTATTTTTAGTAGAG	29116
rs77832768	snp	C/T	0.0391387	0.134304	intron-variant	MYLIP	GRCh38.p7	6:16146204	TGGAGCTGCCACCTA[C/T]GGCTAGAAGCAGAGC	29116
rs77893654	in-del	-/TGG			cds-indel, intron-variant	MYLIP	GRCh38.p7	6:16147744	GTCCTTTTCTGTTTT[-/TGG]GGGGGGAGTTTTGTT	29116
rs78236759	snp	G/T	0.0107246	0.0724382	intron-variant	MYLIP	GRCh38.p7	6:16131553	CAGGAGACTTCAATC[G/T]TACAGTGGCATATCA	29116
rs78468965	in-del	-/AA			intron-variant	MYLIP	GRCh38.p7	6:16138330	CTTTACAAAAAAAAA[-/AA]GGAGGGGGCAAAACC	29116
rs78823578	snp	C/T	0.00755907	0.0610114	intron-variant	MYLIP	GRCh38.p7	6:16130453	GGAATTGTAACACCA[C/T]TGAACTTTGTAAAAA	29116

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