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
rs15514	snp	C/T	0	0	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	SH3D21, THRAP3	GRCh38.p7	1:36304573	AGTGTTCACCTCAGT[C/T]TGGGACCAAACTGCT	79729
rs1875428	snp	C/G	0.0262137	0.111444	missense, utr-variant-5-prime	SH3D21	GRCh38.p7	1:36307267	GCAAGCTGGGGAGAT[C/G]GTGGAAATGATAAAG	79729
rs2282431	snp	C/T	0.489519	0.0716297	intron-variant	SH3D21	GRCh38.p7	1:36319669	CTTCACCTCCCATCA[C/T]GGCAGGAGGAAGAGC	79729
rs2358728	snp	A/G	0.0206156	0.0994123	missense	SH3D21	GRCh38.p7	1:36320254	GTGCCTCTGGCGTGT[A/G]GTCCTCCTCCTGGGA	79729
rs2358729	snp	G/T	0.0206694	0.0995363	missense	SH3D21	GRCh38.p7	1:36320252	GCCTCTGGCGTGTAG[G/T]CCTCCTCCTGGGATG	79729
rs2937378	snp	C/G	0.0337553	0.125452	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	SH3D21, THRAP3	GRCh38.p7	1:36305205	AAGCAGCACAACAAC[C/G]CAAGAGGCAAAGGCT	79729
rs2995227	snp	A/G	0.0337553	0.125452	intron-variant	SH3D21	GRCh38.p7	1:36312066	ctgcactccagcctg[A/G]gtgacaaagcaagac	79729
rs2995228	snp	G/T	0.0821764	0.185298	intron-variant	SH3D21	GRCh38.p7	1:36311841	ctgcacatggtggct[G/T]gtacctgtagtacca	79729
rs2995229	snp	A/C/G	0.0252579	0.109511	intron-variant	SH3D21	GRCh38.p7	1:36307989	AGTGGCTGAGGGAGT[A/C/G]GGGGACCCTTTGGAT	79729
rs3193856	snp	A/G	0.020149	0.0983287	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	SH3D21, THRAP3	GRCh38.p7	1:36305326	GTTTCAACTCCTCCT[A/G]CAAATAAAATAAATG	79729
rs4363401	snp	A/C/G	0.00517822	0.0506191	intron-variant	SH3D21	GRCh38.p7	1:36316923	CTCCCAGTGGCTCAC[A/C/G]CCTGTAATCCCAGTG	79729
rs4652905	snp	A/G	0.32627	0.238082	intron-variant	SH3D21	GRCh38.p7	1:36311120	cactgtgttgcccag[A/G]ctggtcttgaactcc	79729
rs6425980	snp	G/T	0.140242	0.224618	intron-variant	SH3D21	GRCh38.p7	1:36310914	ttggtttgtttgttt[G/T]tttttttttatggag	79729
rs7513452	snp	A/G			intron-variant	SH3D21	GRCh38.p7	1:36315225	aggttgtagtgagcc[A/G]agatcacgccactgc	79729
rs7515833	snp	C/T			intron-variant	SH3D21	GRCh38.p7	1:36315216	gtgaggtggaggttg[C/T]agtgagccaagatca	79729
rs7521070	snp	C/T	0.00755907	0.0610114	utr-variant-3-prime, downstream-variant-500B, intron-variant	SH3D21	GRCh38.p7	1:36321262	CGCTGGGGGCGGGGC[C/T]TGCGCGGGGGCAGGG	79729
rs7523758	snp	A/G			intron-variant	SH3D21	GRCh38.p7	1:36315239	caagatcacgccact[A/G]cactccagcctaggt	79729
rs7546872	snp	C/T			intron-variant	SH3D21	GRCh38.p7	1:36315224	gaggttgtagtgagc[C/T]aagatcacgccactg	79729
rs7546876	snp	C/T	0.000399281	0.0141238	intron-variant	SH3D21	GRCh38.p7	1:36315232	agtgagccaagatca[C/T]gccactgcactccag	79729
rs9633315	snp	C/T	0.138207	0.223612	intron-variant	SH3D21	GRCh38.p7	1:36314043	gcagtggtgcgatct[C/T]ggctcactgcaagct	79729
rs10796880	snp	C/T	0.210139	0.247182	intron-variant	SH3D21	GRCh38.p7	1:36316530	GTGAGCCACCGCGCC[C/T]GGCCGAGAATTTGCT	79729
rs10796881	snp	A/G	0.330249	0.23677	intron-variant, downstream-variant-500B	SH3D21, EVA1B	GRCh38.p7	1:36321693	AGCCTCGAGGTCAGG[A/G]TCCTGAGGCCTGGTG	79729
rs10908294	snp	C/G	0.393987	0.204372	intron-variant	SH3D21	GRCh38.p7	1:36310057	CCTCCTGGGTTCACA[C/G]CATTCTTCTGCCTCA	79729
rs10908295	snp	C/T	0.326035	0.238157	intron-variant	SH3D21	GRCh38.p7	1:36310144	TATTTTTAATAGAGA[C/T]GGGGTTTCACCATGT	79729
rs10908296	snp	C/T			intron-variant	SH3D21	GRCh38.p7	1:36313972	tgctgaacatatttt[C/T]ttttttttttttttt	79729
rs10908297	snp	C/T	0.330016	0.236849	intron-variant	SH3D21	GRCh38.p7	1:36315459	ggttcaagcgattct[C/T]ccgccttagccttct	79729
rs11263871	snp	C/G	0.0498589	0.149812	intron-variant	SH3D21	GRCh38.p7	1:36308218	CAGCAAGGTGTGAGA[C/G]GAACAGGGTGGGGGG	79729
rs11545215	snp	A/T			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	SH3D21, THRAP3	GRCh38.p7	1:36304547	ACACTTCAAAGTTTA[A/T]TCACATGCTTTTGTT	79729
rs11545217	snp	C/T			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	SH3D21, THRAP3	GRCh38.p7	1:36304526	TGCTTTTGTTTTCTC[C/T]TTCAAGAATCAAAGT	79729
rs11545220	snp	A/T			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	SH3D21, THRAP3	GRCh38.p7	1:36305032	AACTTAAACAGCTTA[A/T]GGTTAAAAAGACAAA	79729
rs11589426	snp	G/T			intron-variant	SH3D21	GRCh38.p7	1:36314178	gacggggtttcactg[G/T]gttagccaggatggt	79729
rs11590739	snp	A/G	0.0112356	0.0741051	intron-variant	SH3D21	GRCh38.p7	1:36314314	cttatttcttttgga[A/G]aaatgtctgtttgga	79729
rs11811625	snp	A/G	0.00795532	0.062565	intron-variant	SH3D21	GRCh38.p7	1:36313690	ccacttcagcctccc[A/G]agtagctaggactat	79729
rs12024608	snp	A/G			intron-variant	SH3D21	GRCh38.p7	1:36318630	atacaaaaattggcc[A/G]ggcgcagtggctcac	79729
rs12121759	snp	G/T	0.00766272	0.0614218	missense	SH3D21	GRCh38.p7	1:36320374	TTGAAGTCTGGGCCA[G/T]CATCCAGGCCTGCCC	79729
rs12142928	snp	A/G			intron-variant	SH3D21	GRCh38.p7	1:36315419	taatggcatgatctc[A/G]gctcactgcaacccc	79729
rs12401449	snp	C/G			intron-variant	SH3D21	GRCh38.p7	1:36310594	tatgccagcgtaggt[C/G]agagtgagactctgt	79729
rs12401872	snp	C/T	0.0471551	0.14613	utr-variant-3-prime, nc-transcript-variant	THRAP3	GRCh38.p7	1:36304316	GGTAGGGCGGGAGAG[C/T]GATGCTTGGATTTTT	79729
rs12401880	snp	C/G	0	0	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	THRAP3, SH3D21	GRCh38.p7	1:36304382	TCATTTCATTTGGAG[C/G]TAAGATGACTAATTT	79729
rs12563680	snp	G/T	0.0213498	0.10109	utr-variant-3-prime, nc-transcript-variant, intron-variant, downstream-variant-500B	EVA1B, SH3D21	GRCh38.p7	1:36322253	CTGAGCTCATGTGCA[G/T]GTCCGGTACCCCGAG	79729
rs12726374	snp	A/G			intron-variant	SH3D21	GRCh38.p7	1:36318693	caggtggatcacgag[A/G]tcaggagatgagacc	79729
rs12726546	snp	A/G			intron-variant	SH3D21	GRCh38.p7	1:36318817	gggaggctgaggcag[A/G]agaatggcgtgaacc	79729
rs12726559	snp	A/C			intron-variant	SH3D21	GRCh38.p7	1:36318833	agaatggcgtgaacc[A/C]gggaggcagagcttg	79729
rs12726567	snp	A/G			intron-variant	SH3D21	GRCh38.p7	1:36318850	ggaggcagagcttgc[A/G]gtgagccgagatcgc	79729
rs12726727	snp	A/C			intron-variant	SH3D21	GRCh38.p7	1:36318941	aataataataataat[A/C]caaaaattagccggg	79729
rs12743857	snp	C/G			intron-variant	SH3D21	GRCh38.p7	1:36318667	aatcccagcactttg[C/G]gaggccaaggcaggt	79729
rs12744175	snp	A/G	0.00597247	0.0543191	intron-variant	SH3D21	GRCh38.p7	1:36318876	atcgcaccactgggc[A/G]acagaagcaagactc	79729
rs12745177	snp	C/G			intron-variant	SH3D21	GRCh38.p7	1:36318845	accagggaggcagag[C/G]ttgcagtgagccgag	79729
rs16822736	snp	A/G	0.00560117	0.0526233	intron-variant	THRAP3	GRCh38.p7	1:36303779	CTGGCACTGATGGCA[A/G]TTTTCTTTCCCCTCA	79729
rs28517358	snp	C/G			intron-variant	SH3D21	GRCh38.p7	1:36315130	AAAATACAAAAATTA[C/G]CAGGGCGTGGTGGCG	79729
rs34474512	in-del	-/T	0.486725	0.0803809	intron-variant	SH3D21	GRCh38.p7	1:36316764	TTTTTTTTTTTTTTT[-/T]GGAGACTGAGTTTTG	79729
rs34502139	in-del	-/TG	0.469148	0.120308	intron-variant	SH3D21	GRCh38.p7	1:36309763	ATGTGTGGGTCAGTT[-/TG]TGTGTGTGTTAATAT	79729
rs34586310	in-del	-/C			intron-variant	SH3D21	GRCh38.p7	1:36316888	CTGCCTCAGCCCCCC[-/C]ACGTAGCTGGGACTG	79729
rs35265509	in-del	-/C			intron-variant	SH3D21	GRCh38.p7	1:36320892	CACCTGCCCAGCCCC[-/C]TCACCTCCGCCTCGG	79729
rs35343437	snp	G/T	0.495347	0.0480114	synonymous-codon, utr-variant-5-prime	SH3D21	GRCh38.p7	1:36307804	GCCTTCAGTCAGCCC[G/T]GGTCCCCAGCGGCCT	79729
rs35758712	snp	C/G	0.0540123	0.155206	missense	SH3D21	GRCh38.p7	1:36320677	GGACCAGCGAGGGGA[C/G]CGCGAGCGTCTCTTG	79729
rs36090381	in-del	-/G			intron-variant	SH3D21	GRCh38.p7	1:36308918	TTGTGCCATTGCACT[-/G]CCAGCCTAGGCAACA	79729
rs36123819	in-del	-/A			intron-variant	SH3D21	GRCh38.p7	1:36308916	AGATTGTGCCATTGC[-/A]CTCCAGCCTAGGCAA	79729
rs41267279	snp	A/C/G	0.0129138	0.0793114	synonymous-codon, nc-transcript-variant	THRAP3	GRCh38.p7	1:36303969	AGACGACGAGAGTGG[A/C/G]ACAGAGAACCGAGAA	79729
rs41267281	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	THRAP3	GRCh38.p7	1:36304155	CACAGATTGTACTAC[C/T]GCGAGAGGCATCCCT	79729
rs41267283	snp	C/T	0.0023933	0.0345097	intron-variant, downstream-variant-500B	SH3D21, EVA1B	GRCh38.p7	1:36321622	ACCTCGGCGCAGACG[C/T]GAAGTCCACCGTCCA	79729
rs55662579	in-del	-/TT			intron-variant	SH3D21	GRCh38.p7	1:36316779	TTTTTTTTTTTTTTT[-/TT]GGAGACTGAGTTTTG	79729
rs55667179	snp	C/T	0.117886	0.21224	intron-variant	SH3D21	GRCh38.p7	1:36312005	TGGCTTAGTTTTATA[C/T]ATAAAACTATAATTT	79729
rs55766604	in-del	-/A			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	SH3D21, THRAP3	GRCh38.p7	1:36305029	TTCTTTGTCTTTTTA[-/A]CCTTAAGCTGTTTAA	79729
rs56037315	snp	A/T			intron-variant	SH3D21	GRCh38.p7	1:36309966	ATCTTTTTTTATTTA[A/T]TTTTTTGAGACGGAG	79729
rs56070124	snp	A/T			intron-variant	SH3D21	GRCh38.p7	1:36309962	ATTTATCTTTTTTTA[A/T]TTATTTTTTTGAGAC	79729
rs56161529	snp	A/G	0.46974	0.119223	intron-variant	SH3D21	GRCh38.p7	1:36313998	TTTTTTTTTTGAGAC[A/G]GAGTCTCGCTCTGTC	79729
rs56283418	in-del	-/T			intron-variant	SH3D21	GRCh38.p7	1:36314480	TTTTTTTTTTTTTTT[-/T]AGTCTTGCTCTGTCA	79729
rs58567392	in-del	-/ATAATAATA			intron-variant	SH3D21	GRCh38.p7	1:36318933	ATAATAATAATAATA[-/ATAATAATA]CAAAAATTAGCCGGG	79729
rs58971913	snp	A/G	0.499947	0.0051331	utr-variant-3-prime, nc-transcript-variant, intron-variant, downstream-variant-500B	EVA1B, SH3D21	GRCh38.p7	1:36322287	CTTGCAGCGGGAGCC[A/G]GGGCCCATCAGTAAT	79729
rs59186823	snp	A/C	0.0178098	0.0926698	intron-variant	SH3D21	GRCh38.p7	1:36310647	ACACCCACGAACACC[A/C]ATGGTATGTCACCTA	79729
rs59279425	in-del	-/TTTTGTTTTG			intron-variant	SH3D21	GRCh38.p7	1:36316244	TTTTGTTTTGTTTTG[-/TTTTGTTTTG]AGATGAAGTCTCGCT	79729
rs59524423	snp	G/T			intron-variant	SH3D21	GRCh38.p7	1:36315063	GCAGATTGCTTGAGG[G/T]CAGGAGTTTGAGAAC	79729
rs59853641	in-del	-/A			intron-variant	SH3D21	GRCh38.p7	1:36311553	CTAAAACCTTTAAAA[-/A]TGTTGCTTTTTATAT	79729
rs60993866	in-del	-/ATAA/ATAAATAAATAA/ATAAATAAATAAATAA	0	0	intron-variant	SH3D21	GRCh38.p7	1:36313356	TAAATAAATAAATAA[lengthTooLong]GATGGGAATCATCTT	79729
rs61739316	snp	C/G	0.000133793	0.00817792	synonymous-codon, nc-transcript-variant	THRAP3	GRCh38.p7	1:36303909	ATCAAGTACCAGCCC[C/G]AAGTGGGCCCATGAC	79729
rs61769556	snp	G/T			intron-variant	SH3D21	GRCh38.p7	1:36316235	GCTTTTATTTTTTGT[G/T]TTGTTTTGTTTTGTT	79729
rs63038162	snp	G/T			intron-variant	SH3D21	GRCh38.p7	1:36316780	TTTTTTTTTTTTTTT[G/T]GGAGACTGAGTTTTG	79729
rs71053921	in-del	-/AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	0	0	intron-variant	SH3D21	GRCh38.p7	1:36313992	GCGAGACTCTGTCTC[lengthTooLong]AAAAAAAAAAAAAAA	79729
rs71651910	snp	C/T	0.5	0	intron-variant	SH3D21	GRCh38.p7	1:36310666	GTATGTCACCTAAAC[C/T]TAAGGACTAGAACAT	79729
rs72663437	snp	A/T	0.0107246	0.0724382	intron-variant	SH3D21	GRCh38.p7	1:36317429	TCAGCACTTGTGCAC[A/T]TGCCAGAGTGGCTGT	79729
rs74064531	snp	C/G	0.00279162	0.0372561	intron-variant, downstream-variant-500B	SH3D21, EVA1B	GRCh38.p7	1:36321821	GCGCGCGCGCTTGCT[C/G]TGTGTGTGAGGCTGG	79729
rs74418501	snp	G/T			intron-variant	SH3D21	GRCh38.p7	1:36312722	TTTCTTCTTTTTACT[G/T]TCTTTTGAGACAGAG	79729
rs74842223	snp	C/G			intron-variant	SH3D21	GRCh38.p7	1:36311400	CGCCTGCCATCACGC[C/G]CAGCTAATTTTTTGT	79729
rs75621883	snp	A/C	0.5	0	intron-variant	SH3D21	GRCh38.p7	1:36310613	GTGAGACTCTGTCTC[A/C]AAAAAAAAAAAAAAA	79729
rs75716416	snp	C/T			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	SH3D21, THRAP3	GRCh38.p7	1:36304464	TTTTTTTTTTTTTTT[C/T]TTTTTTTAGGCATAT	79729
rs75851603	snp	A/C	0.5	0	intron-variant	SH3D21	GRCh38.p7	1:36310612	AGTGAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA	79729
rs76280545	snp	A/C	1.65343e-05	0.00287521	missense	SH3D21	GRCh38.p7	1:36320626	GAAAGAGCCTTTGCC[A/C]AAAAAACACGTCCTA	79729
rs76394222	snp	A/G	0.117886	0.21224	intron-variant	SH3D21	GRCh38.p7	1:36313414	TAAATTCATCTTGCC[A/G]TATTTTTTTTCATTA	79729
rs76395550	snp	A/C	0.5	0	intron-variant	SH3D21	GRCh38.p7	1:36310614	TGAGACTCTGTCTCA[A/C]AAAAAAAAAAAAAAT	79729
rs76695875	snp	C/G	0.0102685	0.070914	missense, intron-variant	SH3D21	GRCh38.p7	1:36308160	ACCAGCCTGAGGCCC[C/G]AGACGAGTTGGCGCT	79729
rs77394798	snp	A/G	0.0178098	0.0926698	intron-variant	SH3D21	GRCh38.p7	1:36318152	CAGGATTTGCTGATG[A/G]TTTGGATGTGTCTCA	79729
rs77460292	snp	A/C	0.124491	0.216211	intron-variant	SH3D21	GRCh38.p7	1:36317534	CTGGCCACCCCATTT[A/C]AAATGGTTCCTTCCT	79729
rs77858929	snp	C/T	0.02016	0.0983543	utr-variant-3-prime, nc-transcript-variant	THRAP3	GRCh38.p7	1:36304251	GCAGAATACAACGCA[C/T]TGGGCTTTAGCTGTT	79729
rs78206872	in-del	-/TTT			upstream-variant-2KB, cds-indel, nc-transcript-variant	SH3D21, THRAP3	GRCh38.p7	1:36304461	CTTTTTTTTTTTTTT[-/TTT]CTTTTTTTAGGCATA	79729
rs78276773	snp	A/T			intron-variant	SH3D21	GRCh38.p7	1:36316244	TTTTGTTTTGTTTTG[A/T]TTTGTTTTGAGATGA	79729
rs78549594	snp	A/C/T	0.000798403	0.0199641	intron-variant	SH3D21	GRCh38.p7	1:36319622	GTGAAGTCTCCCAGG[A/C/T]CAAGGGGAACCAGAC	79729
rs79631927	snp	C/T	0.0138799	0.0821421	intron-variant	SH3D21	GRCh38.p7	1:36316033	TTCAAATGTTTTATA[C/T]GTATCTATGCAGTGT	79729
rs111616705	snp	C/G	0.5	0	intron-variant	SH3D21	GRCh38.p7	1:36313229	CTCGGGAAGCTGAGA[C/G]AGGAGAATTGCTTGT	79729
rs112186668	snp	C/G	0.5	0	intron-variant	SH3D21	GRCh38.p7	1:36317207	ACTCAGACCTCACAA[C/G]CACCCTACAAGGTGT	79729

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