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
rs14852	snp	A/G	0	0	utr-variant-3-prime	MNAT1	GRCh38.p7	14:60968589	TAGCCTCATCTGATG[A/G]AAGAGAGGAATAAAT	4331
rs752571	snp	A/C	0.242201	0.249878	intron-variant	MNAT1	GRCh38.p7	14:60905626	GTCTCCATTCTCAGG[A/C]CTTCAACCTCAAACT	4331
rs753014	snp	A/G	0.232651	0.249397	intron-variant	MNAT1	GRCh38.p7	14:60904862	TACTTCTCCCGTATC[A/G]TGGTAGAATTCAGTA	4331
rs913482	snp	C/T	0.232359	0.249377	intron-variant	MNAT1	GRCh38.p7	14:60906942	ggagcttggggatga[C/T]tgtaaaactcaaagt	4331
rs913483	snp	A/C	0.197393	0.244402	intron-variant	MNAT1	GRCh38.p7	14:60904541	TGTTGATGAAAGAAG[A/C]TTGTTTGACAACTGC	4331
rs958015	snp	G/T	0.0138799	0.0821421	intron-variant	MNAT1	GRCh38.p7	14:60822831	ggacagaggttgcag[G/T]gagtccagattgtgt	4331
rs958016	snp	C/T	0.191147	0.242974	intron-variant	MNAT1	GRCh38.p7	14:60822793	ctccagcctggtcga[C/T]agaccaagactccat	4331
rs972758	snp	A/G	0.283947	0.247685	intron-variant	MNAT1	GRCh38.p7	14:60941990	TTGAGATGGAGCCTC[A/G]TTCTGTCGCCCAGGC	4331
rs973063	snp	C/T	0.472709	0.11358	intron-variant	MNAT1	GRCh38.p7	14:60818634	ATTATGTCTTTTCCA[C/T]AAGCATTTCATGTCA	4331
rs975182	snp	C/T	0.29432	0.24604	intron-variant	MNAT1	GRCh38.p7	14:60943772	ATACCTTGCATAAAT[C/T]TGAAAACTTAAAATG	4331
rs1013670	snp	A/G	0.211819	0.247067	intron-variant	MNAT1	GRCh38.p7	14:60827039	TCAGTTTGCAAACAA[A/G]CAAAATAGAATGAAG	4331
rs1028897	snp	A/T	0.308661	0.24302	intron-variant	MNAT1	GRCh38.p7	14:60966489	AATATTTTCTCCATA[A/T]ACTGTATCTTACATA	4331
rs1028898	snp	A/G	0.278664	0.248351	intron-variant	MNAT1	GRCh38.p7	14:60966439	ACTTTAGAGACTACT[A/G]TTATTAATTAGTCAT	4331
rs1033738	snp	G/T	0.0103295	0.0711199	intron-variant	MNAT1	GRCh38.p7	14:60758607	TTTCTGAATTTGGGG[G/T]TTTTTTTTTGGAGGG	4331
rs1051083	snp	A/C	0	0	utr-variant-3-prime	MNAT1	GRCh38.p7	14:60968610	AGGAATAAATAATTC[A/C]CCTATATGTGTTTGA	4331
rs1115839	snp	A/C			intron-variant	MNAT1	GRCh38.p7	14:60846747	ggccataacataagt[A/C]acggtaaattttaaa	4331
rs1116402	snp	A/G	0.0107246	0.0724382	intron-variant	MNAT1	GRCh38.p7	14:60884628	ataaatagaacaaca[A/G]aaagttaaaaagcaa	4331
rs1475020	snp	C/T	0.329317	0.237084	intron-variant	MNAT1	GRCh38.p7	14:60792782	CAGAATGACATCCTT[C/T]TTCTCTCTGAATGAC	4331
rs1475456	snp	C/T	0.000399281	0.0141238	intron-variant	MNAT1	GRCh38.p7	14:60896876	TCAACACTTTGCCAA[C/T]AAGTCTTTTTTTTTT	4331
rs1536713	snp	A/C	0.102014	0.201495	intron-variant	MNAT1	GRCh38.p7	14:60929386	TTACAGGAAAACATA[A/C]GAGGAAATCTTCTTG	4331
rs1571388	snp	G/T	0.328382	0.237395	intron-variant	MNAT1	GRCh38.p7	14:60935827	AGCTTGATGTTCAAT[G/T]TCCTTATCTACAGGG	4331
rs1571389	snp	C/T	0.197082	0.244335	intron-variant	MNAT1	GRCh38.p7	14:60880557	CCCACTTTTTTTTCA[C/T]AGTATATTCTTTCCA	4331
rs1571390	snp	A/G	0.258288	0.249863	intron-variant	MNAT1	GRCh38.p7	14:60850615	GTAAGGTTATTCCAA[A/G]CATGAATAAGGTTAT	4331
rs1801614	snp	A/G			intron-variant	MNAT1	GRCh38.p7	14:60780406	GGTGACATTTCTGCC[A/G]CTGTTGGAAGTTTCT	4331
rs1885093	snp	A/C	0.230896	0.249269	intron-variant	MNAT1	GRCh38.p7	14:60752509	AAATAAGAAGATAAA[A/C]ATTAAAAGAACTCCT	4331
rs1887741	snp	C/T	0.191775	0.243125	intron-variant	MNAT1	GRCh38.p7	14:60867942	CACACAATTTCATGG[C/T]AAGTATAATTCATTT	4331
rs1951108	snp	C/T	0.32955	0.237006	intron-variant	MNAT1	GRCh38.p7	14:60751521	CTAGTTGACATCTGA[C/T]TATACCTCAAAAACC	4331
rs1951110	snp	A/G	0.230017	0.2492	intron-variant	MNAT1	GRCh38.p7	14:60778033	ACCCACTATCACCAA[A/G]TTAGACCCAGCACAG	4331
rs1951111	snp	C/T			intron-variant	MNAT1	GRCh38.p7	14:60773660	GTTCTTTCTGACTTT[C/T]TGAATGGGGCAGTTT	4331
rs1952401	snp	A/T			intron-variant	MNAT1	GRCh38.p7	14:60869042	AAAAAAAAAAAAAAA[A/T]ATATATATATATATA	4331
rs1952402	snp	C/G	0.116138	0.211142	intron-variant	MNAT1	GRCh38.p7	14:60868323	TCAATTGAAGTAATT[C/G]TGAATGACTATTTCT	4331
rs1952404	snp	C/T	0.030665	0.119967	intron-variant	MNAT1	GRCh38.p7	14:60949235	CCCGCTACAATTAGT[C/T]AACAGGAAGTAAAGA	4331
rs1952405	snp	A/G			intron-variant	MNAT1	GRCh38.p7	14:60948936	CTGGAAGGAAATTTT[A/G]AAATCATCTTATCTT	4331
rs1956866	snp	C/T	0	0	intron-variant	MNAT1	GRCh38.p7	14:60759537	CTCATCAACTCCATG[C/T]TGTTGAGAATATGGA	4331
rs1956867	snp	A/G	0.0138799	0.0821421	intron-variant	MNAT1	GRCh38.p7	14:60829104	tccaccaacctctgg[A/G]aagaggtgaggggca	4331
rs1956868	snp	C/T	0.243919	0.249926	intron-variant	MNAT1	GRCh38.p7	14:60764770	AGCTACTACCATTTG[C/T]TAATTTATTTATTTG	4331
rs1956869	snp	C/T	0.188946	0.24243	intron-variant	MNAT1	GRCh38.p7	14:60764676	AATTACATTCTTCAC[C/T]TGGGCATCAAAATCC	4331
rs1958277	snp	A/G	0.233235	0.249437	intron-variant	MNAT1	GRCh38.p7	14:60892024	ATTTTTAAAAAATTG[A/G]TATCATACAAAGTAT	4331
rs1958278	snp	G/T	0.232651	0.249397	intron-variant	MNAT1	GRCh38.p7	14:60891829	aagccataccaaaac[G/T]tatgggacacagcaa	4331
rs1958279	snp	C/T	0.464523	0.128375	intron-variant	MNAT1	GRCh38.p7	14:60883755	actataaaatactga[C/T]gcaaaaaattgaaga	4331
rs1958282	snp	C/T	0	0	intron-variant	MNAT1	GRCh38.p7	14:60963531	ATTTACATTAACAAC[C/T]TGAAGCCTACCTCAG	4331
rs1958283	snp	A/G	0.278664	0.248351	intron-variant	MNAT1	GRCh38.p7	14:60947669	TTCAGATAGAGTCTC[A/G]CTTTGTTGCCGAGGC	4331
rs1958284	snp	C/T	0.215446	0.2476	intron-variant	MNAT1	GRCh38.p7	14:60928428	aaaacagtttggcag[C/T]ttctgaaaagttaaa	4331
rs1963207	snp	A/C	0	0	intron-variant	MNAT1	GRCh38.p7	14:60832581	TTTTGATTACTGTAG[A/C]CTTGTAGTATTGTTT	4331
rs1964900	snp	C/G	0.278664	0.248351	intron-variant	MNAT1	GRCh38.p7	14:60966547	ccagcctgggtgaca[C/G]agcgagactccatct	4331
rs1964901	snp	C/G	0.232651	0.249397	intron-variant	MNAT1	GRCh38.p7	14:60903966	gagaattgcttgaac[C/G]tgggaggcagaagtt	4331
rs1980896	snp	G/T	0.276267	0.248616	intron-variant	MNAT1	GRCh38.p7	14:60964560	AAATATGTGTAAATC[G/T]TATAAGCAGAAACCA	4331
rs1986118	snp	A/G	0	0	intron-variant	MNAT1	GRCh38.p7	14:60826316	aaaaaaaaaaaaaaa[A/G]aaaaaaaaTTTCTCC	4331
rs1999054	snp	C/T	0.226484	0.248892	intron-variant	MNAT1	GRCh38.p7	14:60902912	AAAAACCCAGATATT[C/T]ACCTAATAGAACTAG	4331
rs2020890	snp	C/T	0.0433309	0.140669	intron-variant	MNAT1	GRCh38.p7	14:60818699	TTTTTACATTTCTTA[C/T]TGAACTTGAACTATT	4331
rs2020891	snp	C/T	0.277778	0.248452	synonymous-codon, utr-variant-5-prime	MNAT1	GRCh38.p7	14:60734917	TATCGGAACCCCTCC[C/T]TGAAGCTGATGGTGA	4331
rs2020892	snp	A/G	0.432891	0.170444	intron-variant	MNAT1	GRCh38.p7	14:60811966	AATTTATTCCACGCC[A/G]TATATAAATTTTTGT	4331
rs2025966	snp	C/T	0.00914312	0.0669923	intron-variant	MNAT1	GRCh38.p7	14:60924563	CATATTATTGTTTCT[C/T]CATTTTAAAAGTAGA	4331
rs2025967	snp	A/G	0.459574	0.136304	intron-variant	MNAT1	GRCh38.p7	14:60866645	TATTTGTGGTCACAT[A/G]CAATTACTTTTGAGA	4331
rs2057318	snp	C/T	0.188	0.24219	intron-variant	MNAT1	GRCh38.p7	14:60764169	AGATATATCATACCA[C/T]TAACAAATATTACAT	4331
rs2057319	snp	A/C	0.188	0.24219	intron-variant	MNAT1	GRCh38.p7	14:60764162	TCATACCACTAACAA[A/C]TATTACATAACACTC	4331
rs2057320	snp	G/T	0	0	upstream-variant-2KB	MNAT1	GRCh38.p7	14:60733870	CTTTTCAATAAAAAG[G/T]AATATTCAATTCACA	4331
rs2057321	snp	C/T	0.186421	0.24178	upstream-variant-2KB	MNAT1	GRCh38.p7	14:60733867	TTCAATAAAAAGTAA[C/T]ATTCAATTCACATTT	4331
rs2093250	snp	A/T	0.460027	0.135605	intron-variant	MNAT1	GRCh38.p7	14:60855935	ggagaaggagagaga[A/T]gagagatggggcaat	4331
rs2093251	snp	A/G	0.460365	0.13508	intron-variant	MNAT1	GRCh38.p7	14:60855853	tgggtgtggttcctg[A/G]cagcctaaaacaatt	4331
rs2094552	snp	A/G	0.241914	0.249869	intron-variant	MNAT1	GRCh38.p7	14:60905957	TACTAATTATCATAT[A/G]Gaattttatgtgtca	4331
rs2104075	snp	A/T	0.188946	0.24243	intron-variant	MNAT1	GRCh38.p7	14:60826025	TTGAACCCTTCAACT[A/T]TCTCTAGGTTTATTA	4331
rs2104654	snp	A/C	0.287867	0.247116	intron-variant	MNAT1	GRCh38.p7	14:60956039	GCCCAAAGTTACAGT[A/C]AGGATGGAAATAAAG	4331
rs2145537	snp	C/T	0.0138799	0.0821421	intron-variant	MNAT1	GRCh38.p7	14:60828387	TTATAAGTCACAAAC[C/T]CTACCTTCAATCACA	4331
rs2145538	snp	G/T	0	0	intron-variant	MNAT1	GRCh38.p7	14:60828362	ATCACAATTTACTGG[G/T]CTATTATAGTTTTTA	4331
rs2149301	snp	C/G	0.192088	0.2432	intron-variant	MNAT1	GRCh38.p7	14:60880472	TTCACATTTTAAAAT[C/G]AGACCAAGAAATGAT	4331
rs2149304	snp	C/T	0.314787	0.241459	intron-variant	MNAT1	GRCh38.p7	14:60958127	agtatagagtgggca[C/T]ggtggctcaagcctg	4331
rs2149305	snp	C/T	0.481856	0.0935034	intron-variant	MNAT1	GRCh38.p7	14:60958084	tttgggagggtgagg[C/T]gggcagatcacctga	4331
rs2149306	snp	A/G	0	0	intron-variant	MNAT1	GRCh38.p7	14:60944704	AAATTTTATAATTTA[A/G]GCACTTCTTGTATAT	4331
rs2209895	snp	A/G	0.232359	0.249377	intron-variant	MNAT1	GRCh38.p7	14:60905105	agtaggcacttcata[A/G]ctatttgctaaCCGA	4331
rs2209896	snp	C/T	0.241627	0.24986	intron-variant	MNAT1	GRCh38.p7	14:60900810	tgcccaggctgctct[C/T]gaactcttgggctca	4331
rs2225199	snp	C/T	0.232359	0.249377	intron-variant	MNAT1	GRCh38.p7	14:60905092	TAACTATTTGCTAAC[C/T]GACAACCAAATGAAT	4331
rs2268414	snp	A/G	0.0861826	0.188849	intron-variant	MNAT1	GRCh38.p7	14:60761087	AACAAAGAAGTAAAC[A/G]CATTACATATTAATA	4331
rs2277505	snp	A/C	0.00076321	0.0195198	intron-variant	MNAT1	GRCh38.p7	14:60879689	AAATGAAGGAACTTA[A/C]TACCTCTTATTATTA	4331
rs2284702	snp	A/G	0.33875	0.233717	intron-variant	MNAT1	GRCh38.p7	14:60807159	TCAGAACATCAATTT[A/G]TCATAATCACTGTTG	4331
rs2284703	snp	A/C	0.190205	0.242744	intron-variant	MNAT1	GRCh38.p7	14:60806830	TTTACCAACCACTCA[A/C]AATCTACCTCTTGTA	4331
rs2284704	snp	A/G	0.250168	0.25	intron-variant	MNAT1	GRCh38.p7	14:60745150	GGCAACAATTGCCAT[A/G]ACCATGGCCCAGCAA	4331
rs2300466	snp	C/T	0.317692	0.240661	intron-variant	MNAT1	GRCh38.p7	14:60805420	gtaaactacagactt[C/T]gtgtgataatgatat	4331
rs2300467	snp	A/G	0.00119737	0.0244387	intron-variant	MNAT1	GRCh38.p7	14:60804941	TTCAAAACAGTTTAA[A/G]AAACACTGTTTATTA	4331
rs2300468	snp	C/T	0.0107246	0.0724382	intron-variant	MNAT1	GRCh38.p7	14:60804595	CAAGCTACAGCGAGC[C/T]ATGATAGTACCACTG	4331
rs2300469	snp	C/T	0.192401	0.243274	intron-variant	MNAT1	GRCh38.p7	14:60804365	AAAGAACCATAAAAG[C/T]GAATTACTATTTTAA	4331
rs2300470	snp	A/T	0.231189	0.249291	intron-variant, utr-variant-5-prime	MNAT1	GRCh38.p7	14:60799701	TATATATATATATAT[A/T]TTTTTTTAATCATAG	4331
rs2300471	snp	A/G	0.190833	0.242898	intron-variant	MNAT1	GRCh38.p7	14:60797351	AGTCTAAAAAATACT[A/G]GATCAAGAAAATCTG	4331
rs2300472	snp	A/T	0.200492	0.245049	intron-variant	MNAT1	GRCh38.p7	14:60797333	TCAAGAAAATCTGTA[A/T]ATATTGTAATGTACC	4331
rs2300473	snp	A/T	0.21695	0.247806	intron-variant	MNAT1	GRCh38.p7	14:60796981	TATACACACATATAT[A/T]TACTATGCCCATGTG	4331
rs2351273	snp	C/T	0.216048	0.247684	intron-variant	MNAT1	GRCh38.p7	14:60741794	attacaagagtgagc[C/T]gctgtacctggccCc	4331
rs2351274	snp	A/T			intron-variant	MNAT1	GRCh38.p7	14:60773598	ATTACTTCAGGCAAT[A/T]ACAGGCGGACAAACC	4331
rs2351277	snp	A/C	0.251695	0.250295	intron-variant	MNAT1	GRCh38.p7	14:60787392	GCTAACAATCATCTG[A/C]GCCTTCGAAAGTGAC	4331
rs2351278	snp	C/G	0.250168	0.25	intron-variant	MNAT1	GRCh38.p7	14:60788132	tcaatgtcagaatta[C/G]tccttgacccatggg	4331
rs2351279	snp	C/T	0.230017	0.2492	intron-variant	MNAT1	GRCh38.p7	14:60820658	CCACCTCTTATCATC[C/T]TAGGATAATTGCCAT	4331
rs2351280	snp	A/G	0.18989	0.242666	intron-variant	MNAT1	GRCh38.p7	14:60856578	tttgtagctaaagag[A/G]agaagtcaatgcccg	4331
rs2351281	snp	A/G	0.197082	0.244335	intron-variant	MNAT1	GRCh38.p7	14:60880820	AAAGTCCTACAGCCT[A/G]CAAGCATGAAGCCAA	4331
rs2351536	snp	G/T			intron-variant	MNAT1	GRCh38.p7	14:60904994	TTTTTTTTTTTTTTT[G/T]GACGGAGTCTCGCTC	4331
rs2351537	snp	C/G	0.258288	0.249863	intron-variant	MNAT1	GRCh38.p7	14:60906572	aatttttgatggatt[C/G]gttaaggggggtatg	4331
rs2351538	snp	A/G	0.261608	0.24973	intron-variant	MNAT1	GRCh38.p7	14:60906610	gaagattacttccaa[A/G]gtttttatctgagca	4331
rs2882684	snp	A/G	0.495174	0.0488838	intron-variant	MNAT1	GRCh38.p7	14:60949744	TTCATTTTTGGTACC[A/G]TTGATTGCATTAGCA	4331
rs2882685	snp	A/C	0.02016	0.0983543	intron-variant	MNAT1	GRCh38.p7	14:60966345	ggctggtctgaaact[A/C]ctgtcctcaggtgat	4331
rs2882703	snp	A/G	0.00517822	0.0506191	intron-variant	MNAT1	GRCh38.p7	14:60924978	TCCCAGTAAGTAAAT[A/G]TGTTACATTGTTAAT	4331
rs3049888	in-del	-/TT/TTTT/TTTTT	0	0	intron-variant	MNAT1	GRCh38.p7	14:60741680	TTTTTTTTTTTTTTT[-/TT/TTTT/TTTTT]AATTTTTAGTAGAGA	4331
rs3049925	in-del	-/TG	0.128419	0.218444	intron-variant	MNAT1	GRCh38.p7	14:60861575	ttttaaaaaaatttG[-/TG]AAAAGGTCTACAGGC	4331

Full records

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