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
rs15307	snp	C/T	0.156319	0.231784	utr-variant-3-prime, nc-transcript-variant	MYSM1	GRCh38.p7	1:58654907	AAAATGTTGTAAATA[C/T]CTGCATTTTAAGAAT	114803
rs232775	snp	A/G	0.456803	0.140473	utr-variant-3-prime, nc-transcript-variant	MYSM1	GRCh38.p7	1:58658874	AAATTCTCTAGATCA[A/G]GGGTTGGAGAATAAT	114803
rs232776	snp	C/T	0.456568	0.140818	utr-variant-3-prime, nc-transcript-variant	MYSM1	GRCh38.p7	1:58659131	GGGCTGAATATGTAA[C/T]ATGTCCTGAAAGGCT	114803
rs232777	snp	C/T	0.365781	0.221574	missense, nc-transcript-variant	MYSM1	GRCh38.p7	1:58660011	ATCACATTAACAATT[C/T]CTTTGTACAGTTCTC	114803
rs232778	snp	A/G	0.156319	0.231784	intron-variant, downstream-variant-500B	MYSM1	GRCh38.p7	1:58660944	CTGCTAAAATCAGCC[A/G]ACACTGACAAATTTA	114803
rs232779	snp	A/C	0.155987	0.23165	intron-variant, downstream-variant-500B	MYSM1	GRCh38.p7	1:58661004	GCTTGGGCAACAAAA[A/C]ACGTTACTAATTATC	114803
rs232780	snp	C/T	0.37518	0.216402	intron-variant	MYSM1	GRCh38.p7	1:58661535	GCATAAAGAAGCACA[C/T]TGTCATCAACTATTT	114803
rs232781	snp	G/T	0.456568	0.140818	intron-variant	MYSM1	GRCh38.p7	1:58661965	CAACAATGCTGTAAG[G/T]TATTGTTTTTTTTTT	114803
rs232782	snp	A/G	0.422473	0.180978	intron-variant	MYSM1	GRCh38.p7	1:58662565	CAGGCAGTCAGGCTC[A/G]AGAGTTCTGCTTTTA	114803
rs232783	snp	G/T	0.187053	0.241946	intron-variant	MYSM1	GRCh38.p7	1:58663844	CACCTTAATTGAGTC[G/T]GCCTGGCTCTGGGTG	114803
rs232784	snp	A/C	0.187053	0.241946	intron-variant	MYSM1	GRCh38.p7	1:58663972	TATTCCTTTGCTGCT[A/C]AATGTTGTGTTTAAA	114803
rs232785	snp	A/G	0.422315	0.181128	intron-variant	MYSM1	GRCh38.p7	1:58664301	GAGCTAAAGAATAAT[A/G]TGTATTATGTGCTAT	114803
rs232786	snp	A/C	0.424968	0.178567	intron-variant	MYSM1	GRCh38.p7	1:58664557	TGTTGCAGATACATA[A/C]AGAATAAAGCAACTA	114803
rs232787	snp	C/T	0.421842	0.181577	intron-variant	MYSM1	GRCh38.p7	1:58664735	TAGAAAAAATGGGTA[C/T]AATACAGTATTTATT	114803
rs232788	snp	C/T	0.187053	0.241946	intron-variant	MYSM1	GRCh38.p7	1:58664942	AGTCTGCTATACTAA[C/T]TCCCTATCCGCCCAG	114803
rs232789	snp	A/G	0.422	0.181428	intron-variant	MYSM1	GRCh38.p7	1:58664992	GGACATAAACCTCAG[A/G]GGAATCAAGTCAGAT	114803
rs232790	snp	G/T	0.190623	0.242847	intron-variant	MYSM1	GRCh38.p7	1:58665639	AAGTAACTCTACAAT[G/T]ACAAGAAAAATATAA	114803
rs232791	snp	C/T	0.457037	0.140127	intron-variant	MYSM1	GRCh38.p7	1:58665809	CAGCACTTTGGGAGA[C/T]TGAGGCAGGCGGACT	114803
rs232792	snp	A/G	0.421842	0.181577	intron-variant	MYSM1	GRCh38.p7	1:58665851	GGTCAGCCTGATCAG[A/G]CTTGAGACCAGCCTG	114803
rs232793	snp	C/T	0.422158	0.181278	intron-variant	MYSM1	GRCh38.p7	1:58666122	GATATTCATCTCACA[C/T]GGTACATTTTTCAGG	114803
rs232794	snp	G/T	0.422315	0.181128	intron-variant	MYSM1	GRCh38.p7	1:58667352	TTAACAATACCACAG[G/T]TGCCTTTAACTTGCA	114803
rs232795	snp	A/G	0.421842	0.181577	intron-variant	MYSM1	GRCh38.p7	1:58667596	CCTCTTAGAAGTTGT[A/G]GCTTTTTACTAATAA	114803
rs232850	snp	A/G	0.0517044	0.152246	utr-variant-3-prime, nc-transcript-variant	MYSM1	GRCh38.p7	1:58657859	TTGCCCTGTGTGCCA[A/G]TGTTTAACCATATTT	114803
rs232851	snp	A/G	0.456803	0.140473	utr-variant-3-prime, nc-transcript-variant	MYSM1	GRCh38.p7	1:58657199	ACTAGCGCTTCCCCA[A/G]TATTAGACTTAATCT	114803
rs232852	snp	A/C	0.42263	0.180829	utr-variant-3-prime, nc-transcript-variant	MYSM1	GRCh38.p7	1:58656617	TATAGACTTGAACTT[A/C]CTTCCTTCCCAACCT	114803
rs232853	snp	C/G	0.421842	0.181577	utr-variant-3-prime, nc-transcript-variant	MYSM1	GRCh38.p7	1:58656096	CCTCCCATTTCTCTT[C/G]CTGGGTCCTGATGAG	114803
rs232854	snp	A/T	0.422315	0.181128	utr-variant-3-prime, nc-transcript-variant	MYSM1	GRCh38.p7	1:58655671	AGAATAATGTAATAT[A/T]CTTTAGGATATATTT	114803
rs232855	snp	C/T	0.422158	0.181278	utr-variant-3-prime, nc-transcript-variant	MYSM1	GRCh38.p7	1:58655494	GGGAATAAATAGTTG[C/T]CTCCACTAAATCAGG	114803
rs232856	snp	C/T	0.421526	0.181876	utr-variant-3-prime, nc-transcript-variant	MYSM1	GRCh38.p7	1:58655289	TTTTTGACATTTCCT[C/T]GTCTCTTAAGAAGTC	114803
rs232857	snp	A/G	0.157642	0.232314	utr-variant-3-prime, nc-transcript-variant	MYSM1	GRCh38.p7	1:58654978	GTTCTGTGATAAAAT[A/G]TAATTTCAACTATTT	114803
rs232858	snp	A/G	0.422315	0.181128	utr-variant-3-prime, nc-transcript-variant	MYSM1	GRCh38.p7	1:58654917	TCTGTATTTAAAAAT[A/G]TTGTAAATACCTGCA	114803
rs232860	snp	C/T	0.422315	0.181128	utr-variant-3-prime, nc-transcript-variant	MYSM1	GRCh38.p7	1:58654891	CTGCATTTTAAGAAT[C/T]ATGAAAGATTTTCCT	114803
rs232861	snp	A/C	0.45645	0.140991	downstream-variant-500B	MYSM1	GRCh38.p7	1:58654727	GTGATCATTTGGATT[A/C]TTTCTAAATTATTAG	114803
rs471446	snp	C/G/T	0.120674	0.21395	intron-variant	MYSM1	GRCh38.p7	1:58677334	TCCCAGGACCTTGAA[C/G/T]TCAGAAATTTATGTA	114803
rs472129	snp	C/T	0.121369	0.214369	intron-variant	MYSM1	GRCh38.p7	1:58677360	ATGTACAGACACAAA[C/T]TGAATCTTTAAATAC	114803
rs489260	snp	C/T	0.122411	0.214991	intron-variant	MYSM1	GRCh38.p7	1:58674092	tggagtgcagtggcg[C/T]gatctttgcttactg	114803
rs500863	snp	A/G	0.121369	0.214369	intron-variant	MYSM1	GRCh38.p7	1:58678162	GGGACAAACAGGCAT[A/G]GACTACTTTAGATAG	114803
rs506077	snp	A/C	0.456332	0.141164	intron-variant	MYSM1	GRCh38.p7	1:58670757	ATGAGGTTTACATTt[A/C]ttcaattaaacattg	114803
rs506078	snp	C/T	0.456332	0.141164	intron-variant	MYSM1	GRCh38.p7	1:58670759	GAGGTTTACATTTAT[C/T]CAATTAAACATTGCA	114803
rs513436	snp	C/T	0.187369	0.242028	intron-variant	MYSM1	GRCh38.p7	1:58671601	GGTTCCTGTCCATAG[C/T]GTCTAGAGTTGAATG	114803
rs516956	snp	A/G	0.422473	0.180978	intron-variant	MYSM1	GRCh38.p7	1:58665416	GCATTAAATAATTTT[A/G]AACAGTTGCAAATCT	114803
rs516957	snp	A/C	0.422473	0.180978	intron-variant	MYSM1	GRCh38.p7	1:58665417	CATTAAATAATTTTA[A/C]ACAGTTGCAAATCTT	114803
rs519331	snp	A/T	0.121369	0.214369	intron-variant	MYSM1	GRCh38.p7	1:58675051	TGATTTACGAATTTT[A/T]AAATATTATAAAACT	114803
rs522103	snp	A/T	0.0733688	0.176922	intron-variant	MYSM1	GRCh38.p7	1:58675353	TTGCTAAGGTGAAAC[A/T]CAAGAGGAAACATGT	114803
rs527445	snp	C/T	0.456685	0.140646	intron-variant	MYSM1	GRCh38.p7	1:58678807	ACACTTGACAAAATA[C/T]GGGGGAAGAACATCC	114803
rs528387	snp	A/G	0.121369	0.214369	intron-variant	MYSM1	GRCh38.p7	1:58678916	TCTCCTTTACCTAGT[A/G]TGACCTGGAAAAGTT	114803
rs528642	snp	A/C	0.122411	0.214991	intron-variant	MYSM1	GRCh38.p7	1:58669532	CTATCATAAACTCTT[A/C]AAGTGAAAAAGTggc	114803
rs529289	snp	A/G	0.122064	0.214785	intron-variant	MYSM1	GRCh38.p7	1:58679009	TTGGAGATGATTTAA[A/G]TACAGTACATGGTAT	114803
rs539141	snp	A/G	0.456214	0.141336	intron-variant	MYSM1	GRCh38.p7	1:58672111	CCAACATGTAGAAAG[A/G]CTGGACAGTATTTTT	114803
rs542750	snp	C/T	0.187053	0.241946	intron-variant	MYSM1	GRCh38.p7	1:58672500	GTATTATTGTGAAGA[C/T]TGAGTTAATGTTTAT	114803
rs553215	snp	A/C	0	0	intron-variant	MYSM1	GRCh38.p7	1:58669857	AAAAAAAAAAAAAAA[A/C]AAAAACAAAAAAGTG	114803
rs553540	snp	G/T	0.121369	0.214369	intron-variant	MYSM1	GRCh38.p7	1:58676527	ACGCTTTTATCACAT[G/T]TAAGTGTAGAGGCTC	114803
rs554318	snp	C/T	0.456568	0.140818	intron-variant	MYSM1	GRCh38.p7	1:58676576	TTAAACATTGCTAGG[C/T]AGTATTTCTAGCATG	114803
rs556801	snp	A/G	0.00953873	0.0683987	intron-variant	MYSM1	GRCh38.p7	1:58670252	AGAAACTGAAGGCCA[A/G]GATAGATGAGAAAAT	114803
rs568320	snp	A/G	0.122411	0.214991	intron-variant	MYSM1	GRCh38.p7	1:58672964	GAGAACTCAAGTTTG[A/G]GTACTTTGTGCATGC	114803
rs579110	snp	C/T	0.475022	0.108927	synonymous-codon, nc-transcript-variant	MYSM1	GRCh38.p7	1:58677041	CTTATTTAAGTATTT[C/T]GGTTTGCATATCTCC	114803
rs583854	snp	A/G	0.121369	0.214369	intron-variant	MYSM1	GRCh38.p7	1:58679016	TGATTTAAGTACAGT[A/G]CATGGTATTCGGGAG	114803
rs584284	snp	A/G	0.456568	0.140818	intron-variant	MYSM1	GRCh38.p7	1:58679115	TGCTTTTATGAAAAG[A/G]ATCTTTATCTATAAA	114803
rs586509	snp	A/G	0.123105	0.215401	intron-variant	MYSM1	GRCh38.p7	1:58673027	TATATAGTCTATCTC[A/G]TTTCTTTCTTACAAC	114803
rs595083	snp	A/C	0.121369	0.214369	intron-variant	MYSM1	GRCh38.p7	1:58679249	ATGTGAGTTCCTGTT[A/C]AAAACAATTTTTGCT	114803
rs601459	snp	A/G	0.122758	0.215196	intron-variant	MYSM1	GRCh38.p7	1:58674069	gagtctcactgtgtc[A/G]cccaggctggagtgc	114803
rs613810	snp	C/G	0.0119091	0.0762411	intron-variant	MYSM1	GRCh38.p7	1:58674509	TAGAAATGGTTTATA[C/G]CCTAAATACTCTGAG	114803
rs631352	snp	C/G	0.121369	0.214369	intron-variant	MYSM1	GRCh38.p7	1:58676154	TCAGGCGCGGTGGCT[C/G]ACGCCTGTGATCCCA	114803
rs646018	snp	C/T	0.121369	0.214369	intron-variant	MYSM1	GRCh38.p7	1:58677157	ATCTCTAAATTTTAA[C/T]CCCTTTCAATGTATA	114803
rs662989	snp	C/G	0.122411	0.214991	intron-variant	MYSM1	GRCh38.p7	1:58670677	AGATGAAGATATATG[C/G]GTTAATTGTGGTAAT	114803
rs673685	snp	C/T	0.121369	0.214369	intron-variant	MYSM1	GRCh38.p7	1:58677336	CCAGGACCTTGAATT[C/T]AGAAATTTATGTACA	114803
rs674205	snp	C/T	0.121717	0.214577	intron-variant	MYSM1	GRCh38.p7	1:58677455	ACTTAGATTCATCTA[C/T]TCTTATTTTGCTTAA	114803
rs675496	snp	C/T	0.121369	0.214369	intron-variant	MYSM1	GRCh38.p7	1:58677716	GTACAACATAAAATT[C/T]GAGTAATAAAGAACT	114803
rs675871	snp	C/T	0.187369	0.242028	intron-variant	MYSM1	GRCh38.p7	1:58671203	AAATGGGAGTGAGAA[C/T]ATTAACTAATGCACA	114803
rs675919	snp	C/G	0.122411	0.214991	intron-variant	MYSM1	GRCh38.p7	1:58671240	TCATGAAGACTATAT[C/G]AGCTAATAAATATAA	114803
rs678233	snp	C/G	0.122411	0.214991	intron-variant	MYSM1	GRCh38.p7	1:58671757	TAAAAAATTGTAGCA[C/G]TATTTTTTTAAACTT	114803
rs678283	snp	C/T	0.122411	0.214991	intron-variant	MYSM1	GRCh38.p7	1:58671784	ACTTAATGTGAACAA[C/T]ATAATGCAGCTATTG	114803
rs679619	snp	A/T	0.122411	0.214991	intron-variant	MYSM1	GRCh38.p7	1:58672072	GAGAGACTAAATTGA[A/T]ATAGATGGGCTTCCT	114803
rs688158	snp	C/T	0.121369	0.214369	intron-variant	MYSM1	GRCh38.p7	1:58678199	TGCTTAGGCTAGGCC[C/T]CACTAAGCAGAATAG	114803
rs688225	snp	A/C	0.188	0.24219	intron-variant	MYSM1	GRCh38.p7	1:58678252	TGGGAGGGTACCACA[A/C]CTTCCATAGAAACGT	114803
rs1986206	snp	A/T	0.45235	0.146814	intron-variant	MYSM1	GRCh38.p7	1:58666885	TTTATTTTTATTATT[A/T]TTTTTTTTTTGAGAC	114803
rs2029648	snp	A/G	0.486464	0.0811471	intron-variant	MYSM1	GRCh38.p7	1:58674053	GGTTTTTTTTGAGAC[A/G]GAGTCTCACTGTGTC	114803
rs2064370	snp	C/G	0.480864	0.0959265	intron-variant	MYSM1	GRCh38.p7	1:58673551	GTTTTCATGGATGAG[C/G]CATTTGAAAGGTCAA	114803
rs2064371	snp	C/T	0.486595	0.0807641	intron-variant	MYSM1	GRCh38.p7	1:58686343	ATACGTAAATCCTCT[C/T]TGCAATATCCCCAAC	114803
rs2064372	snp	G/T	0.486398	0.0813386	intron-variant	MYSM1	GRCh38.p7	1:58686462	AACTTAGGAAAAGTT[G/T]TGTCAGATTTACAGG	114803
rs2064373	snp	A/C	0.230017	0.2492	intron-variant	MYSM1	GRCh38.p7	1:58695070	AAAAAAAAAAAGAAG[A/C]AGCACTCTAGGCAAT	114803
rs2064374	snp	A/G	0.482249	0.0925224	intron-variant	MYSM1	GRCh38.p7	1:58695213	TTCACCACTTCTGTA[A/G]TAATTAAGAAAATGA	114803
rs2179658	snp	C/T	0.0115144	0.0749975	intron-variant	MYSM1	GRCh38.p7	1:58688004	TTATGTATCTGGTCT[C/T]TGATAAGGGGCAAAA	114803
rs2206764	snp	A/G	0.180963	0.240279	intron-variant	MYSM1	GRCh38.p7	1:58685269	GTATTATTAAAATGG[A/G]AAAAAAAATTGCTTT	114803
rs2206765	snp	C/G	0.489722	0.0709447	intron-variant	MYSM1	GRCh38.p7	1:58685601	CCTGAAAGGGGTACA[C/G]GTTACATTTTCCATT	114803
rs2223698	snp	C/T	0.483636	0.0889627	intron-variant	MYSM1	GRCh38.p7	1:58690011	CACAATCTGAAAGAA[C/T]TGCCTACATAGGGCC	114803
rs2406931	snp	C/T	0.487746	0.0773096	intron-variant	MYSM1	GRCh38.p7	1:58676146	AGTAGAGGTCAGGCG[C/T]GGTGGCTCACGCCTG	114803
rs2473746	snp	A/G	0.449138	0.151142	intron-variant	MYSM1	GRCh38.p7	1:58695063	AGTTTAAAAAAAAAA[A/G]AAGAAGAAGCACTCT	114803
rs2746077	snp	C/T	0.157311	0.232183	intron-variant	MYSM1	GRCh38.p7	1:58687507	ATTTGCAGATGTAAG[C/T]ATATATGTTAGTACA	114803
rs2746078	snp	C/T	0.0599851	0.162463	intron-variant	MYSM1	GRCh38.p7	1:58687659	gcccaactaaagaaa[C/T]atccctatcctatct	114803
rs2746079	snp	C/G	0.0948562	0.196037	intron-variant, upstream-variant-2KB	MYSM1	GRCh38.p7	1:58691835	tcgcaccattgcact[C/G]cagcctgggtgacaa	114803
rs2746080	snp	A/G	0.0952156	0.196321	intron-variant, upstream-variant-2KB	MYSM1	GRCh38.p7	1:58692081	CTCTGAATAGCAATA[A/G]TCTAGGCTATAACTG	114803
rs2746081	snp	A/G	0.465368	0.126951	intron-variant	MYSM1	GRCh38.p7	1:58692489	GAGAAGAACTTTTAC[A/G]TGTTCCAACTCTGTG	114803
rs2746082	snp	C/G	0.465263	0.127129	intron-variant	MYSM1	GRCh38.p7	1:58694611	GGCGACAAAGAGACT[C/G]CATCTCAAAAAAAAA	114803
rs2746083	snp	A/C	0.188	0.24219	intron-variant	MYSM1	GRCh38.p7	1:58696006	CCATCTCTAAGACTG[A/C]AAAAACCTTTCAACA	114803
rs2811859	snp	A/G	0.0599851	0.162463	intron-variant, upstream-variant-2KB	MYSM1	GRCh38.p7	1:58691141	aaaaattagccaggc[A/G]tggtggcgggcgcct	114803
rs2811864	snp	A/G	0.0948562	0.196037	intron-variant, upstream-variant-2KB	MYSM1	GRCh38.p7	1:58692023	attaatttcctttgt[A/G]ttaaatgaggatatc	114803
rs2811871	snp	G/T	0.0948562	0.196037	intron-variant	MYSM1	GRCh38.p7	1:58687633	accacctgactacaa[G/T]acaaacaaaggccca	114803
rs2811889	snp	G/T	0.0944967	0.195752	intron-variant	MYSM1	GRCh38.p7	1:58695836	TAAATTATCTCACTC[G/T]TTTCATTAAGCTCCT	114803
rs2811891	snp	A/G	0.0123036	0.0774623	intron-variant	MYSM1	GRCh38.p7	1:58696277	CCACTATCATTTCAA[A/G]TTCACTGTAGAAATC	114803

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