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
rs3428	snp	C/T	0.0182019	0.0936463	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038741	GATTTTCTCAGGCCT[C/T]TTTTGGATACCTTTA	88455
rs15865	snp	C/T			synonymous-codon, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110027709	CCCCTCTGTAGCAGA[C/T]AGGAACCCGCTGGAA	88455
rs741374	snp	A/G	0	0	intron-variant	ANKRD13A	GRCh38.p7	12:110024575	ACTGGATCAACAATC[A/G]TCTCCACTATTACAA	88455
rs1044994	snp	A/T	0.350982	0.228698	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110038790	TCAAACCCTCTTGTA[A/T]ATAACCATCGCACAA	88455
rs1058777	snp	A/C	0.00795532	0.062565	intron-variant	ANKRD13A	GRCh38.p7	12:110028018	TTTCTATAAAGAGGC[A/C]CCTCGTTTATAATGG	88455
rs1510605	snp	C/T	0.351635	0.228408	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109998104	GCAACTTAACGTTCT[C/T]CTTCTTCTTCATCAT	88455
rs1912516	snp	A/G	0.207864	0.246424	intron-variant	ANKRD13A	GRCh38.p7	12:110001637	AGGCCAGGGGTTGAA[A/G]CCAGCATGGCCAACA	88455
rs2136797	snp	A/G	0.0919752	0.193722	intron-variant	ANKRD13A	GRCh38.p7	12:110004063	TCAAGCGATTCTCCC[A/G]CCTCAGCCTCCCAAG	88455
rs2287173	snp	A/G	0.349671	0.229272	intron-variant	ANKRD13A	GRCh38.p7	12:110018899	GCTAATAAGAATGCA[A/G]ATTATTAAGAAAAAT	88455
rs2287174	snp	C/T	0.0922807	0.193971	missense, synonymous-codon	ANKRD13A	GRCh38.p7	12:110036265	GTCTTTGCCAGGAAC[C/T]TTCAGGACCAGCTTC	88455
rs2287175	snp	C/T	0.119281	0.213102	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037732	CCATCCAGGCTGCTC[C/T]CTGGGGTGGAGAAGG	88455
rs2302689	snp	A/G	0.318164	0.240528	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	ANKRD13A	GRCh38.p7	12:110018370	TTCTAGAATATGCCC[A/G]AATGATGTCTGTCGC	88455
rs3759385	snp	C/T	0.0711525	0.174681	intron-variant	ANKRD13A	GRCh38.p7	12:110011934	AATGTGCTTGACAGA[C/T]ATTTCAAGTACAAAA	88455
rs3759386	snp	C/T	0.246769	0.249979	upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109998346	AGCTGTTCAAGAATC[C/T]CAACCTAATCCATTC	88455
rs4418866	snp	A/G	0.0479149	0.147179	intron-variant	ANKRD13A	GRCh38.p7	12:110007287	ACCTCAGTTTGGAGA[A/G]TTTTGTCATTTTAAC	88455
rs4766427	snp	A/G	0.0763149	0.179815	intron-variant	ANKRD13A	GRCh38.p7	12:110028807	CAGTGGCACGAACTC[A/G]GCTCACTGCAACCTC	88455
rs6606679	snp	C/T	0.401215	0.199083	intron-variant	ANKRD13A	GRCh38.p7	12:110010378	GGAAGATAATGAGTT[C/T]GCTAATTATTTCTTT	88455
rs6606680	snp	A/G	0.426201	0.177351	intron-variant	ANKRD13A	GRCh38.p7	12:110010451	TCTTGTTACTTTTAA[A/G]AAAATATTTAATGCA	88455
rs6606681	snp	C/T	0.240765	0.249829	intron-variant	ANKRD13A	GRCh38.p7	12:110013800	Aaataataataaata[C/T]aataatataataata	88455
rs7295290	snp	C/T	0.12932	0.218944	intron-variant	ANKRD13A	GRCh38.p7	12:110016585	AATCACTGATAGTCC[C/T]AGTTAAACACAACTG	88455
rs7295865	snp	A/T	0.00636936	0.0560724	intron-variant	ANKRD13A	GRCh38.p7	12:110002254	TTTGTAAACCTGGGG[A/T]TTGAGCTTTTTTGCT	88455
rs7299156	snp	C/T	0.354019	0.227333	intron-variant	ANKRD13A	GRCh38.p7	12:110002354	GGGCACGGTGGCTCA[C/T]GCCTGGAATCTCAGC	88455
rs7299483	snp	C/G	0.354019	0.227333	intron-variant	ANKRD13A	GRCh38.p7	12:110005001	GTATAAACATATACA[C/G]ATTGATtttttcaaa	88455
rs7300927	snp	A/G	0.429688	0.173817	intron-variant	ANKRD13A	GRCh38.p7	12:110020727	CCAGAAGGCAGAGGA[A/G]GCTGCCTTTTCTGCC	88455
rs7306815	snp	C/T	0.153997	0.230832	intron-variant	ANKRD13A	GRCh38.p7	12:110009450	tttaattcctgattt[C/T]agtaagttaagtctt	88455
rs7310558	snp	C/T	0.347032	0.230401	intron-variant	ANKRD13A	GRCh38.p7	12:110025070	TTACAAGACTACCAG[C/T]GGAGGCTGGGTGCAG	88455
rs7310812	snp	C/T	0.0205511	0.0992634	intron-variant	ANKRD13A	GRCh38.p7	12:110025263	ctggaggctgaggca[C/T]gagaatcgcttgaac	88455
rs7311261	snp	C/T	0.130694	0.219696	intron-variant	ANKRD13A	GRCh38.p7	12:110010600	ATCATGGGAGGTGTG[C/T]GGACTGGGCTCCAGG	88455
rs7954480	snp	A/G	0.00199481	0.0315187	intron-variant	ANKRD13A	GRCh38.p7	12:110017976	CATTTGATACTCTGA[A/G]TGGTGGATATGACAA	88455
rs7970105	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110014191	gctgaggtgggtgga[C/T]cacgaggtcaggaga	88455
rs7970733	snp	G/T			intron-variant	ANKRD13A	GRCh38.p7	12:110008750	attagccaggtgtgg[G/T]ggtgggcacctgtaa	88455
rs7970988	snp	G/T	0.0205511	0.0992634	intron-variant	ANKRD13A	GRCh38.p7	12:110008917	ggcctgcattttttt[G/T]ggtgggcagttttaa	88455
rs7976412	snp	C/G	0.429538	0.173972	intron-variant	ANKRD13A	GRCh38.p7	12:110012882	ATTATCAGGATTTCG[C/G]AACCAGTGGTAAGAA	88455
rs7976663	snp	C/T	0.154993	0.231244	intron-variant	ANKRD13A	GRCh38.p7	12:110020296	ATCCTGGACTTAGGC[C/T]TTCTTTTCTCTTGAT	88455
rs7977696	snp	A/G	0.36021	0.224397	intron-variant	ANKRD13A	GRCh38.p7	12:110008621	caggcatggtggctc[A/G]tgcctgtaatcccag	88455
rs9630308	snp	A/G/T	0.0212419	0.100845	utr-variant-3-prime	ANKRD13A	GRCh38.p7	12:110037630	TCAACCAGGGCCCTA[A/G/T]GGCTAAGGGCCTGCA	88455
rs10849627	snp	G/T	0.429087	0.174436	intron-variant	ANKRD13A	GRCh38.p7	12:110000433	AAGTTTGAGAATCAC[G/T]GGTTCTCAGGCTCCT	88455
rs11064671	snp	C/T	0.154661	0.231107	intron-variant	ANKRD13A	GRCh38.p7	12:110000714	ggcccccaaagccga[C/T]agcgtcttggttgag	88455
rs11064687	snp	A/G	0.160938	0.233598	intron-variant	ANKRD13A	GRCh38.p7	12:110003925	GCTCTTTGGGAGGCC[A/G]AGGCAGGTGGATCAT	88455
rs11064688	snp	C/T	0.160938	0.233598	intron-variant	ANKRD13A	GRCh38.p7	12:110004036	GGTGGCGGGTGCTTG[C/T]AATCCCAGCTACTTG	88455
rs11064702	snp	A/G	0.154329	0.23097	intron-variant	ANKRD13A	GRCh38.p7	12:110007692	GCCAGTTCTTCTTTA[A/G]TTTTTTTTAAACAAT	88455
rs11064715	snp	G/T	0.148326	0.228391	intron-variant	ANKRD13A	GRCh38.p7	12:110010397	AATTATTTCTTTCCT[G/T]CTAAACTTCAACTGA	88455
rs11064716	snp	A/G	0	0	intron-variant	ANKRD13A	GRCh38.p7	12:110010428	ATTTATAGTTCATAA[A/G]TTCATCGTCTTGTTA	88455
rs11064735	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110017946	caaaaaaaaaaaaaa[A/G]TGGCATACTTTAGAC	88455
rs11064797	snp	A/G	0.128632	0.218563	intron-variant	ANKRD13A	GRCh38.p7	12:110031808	catttccagttacta[A/G]tatatagaaatataa	88455
rs11352479	in-del	-/A	0	0	intron-variant	ANKRD13A	GRCh38.p7	12:110011109	GACCTTGTTTAAAAG[-/A]AAAAAAAAAAAAAGG	88455
rs11395070	in-del	-/T	0.429388	0.174127	intron-variant	ANKRD13A	GRCh38.p7	12:110005006	ACAGATTGATTTTTT[-/T]CAAAAGATTTTTATT	88455
rs11608607	snp	C/T	0.0228947	0.104514	downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110039821	CTATATCTAAATAAG[C/T]GGGTATTAAAAACAA	88455
rs11831498	snp	A/G	0.00795532	0.062565	intron-variant	ANKRD13A	GRCh38.p7	12:110006627	ttgagatggagtttc[A/G]ctcttgttgcctagg	88455
rs12231633	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110026242	agtgctgagattaca[A/G]gcgtgagccaccgtg	88455
rs12231634	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110026245	gctgagattacaggc[A/G]tgagccaccgtgcct	88455
rs12300179	snp	A/T	0.128632	0.218563	intron-variant	ANKRD13A	GRCh38.p7	12:110013320	TGGAGACACAGTTTG[A/T]CATCCTTGTGTGCCT	88455
rs12302340	snp	A/G	0.128632	0.218563	intron-variant	ANKRD13A	GRCh38.p7	12:110008873	ctgggcgacagagcg[A/G]gactcagtctggaaa	88455
rs12303589	snp	A/G	0.0150606	0.0854603	intron-variant	ANKRD13A	GRCh38.p7	12:110031566	atgttggctaggctg[A/G]tctggaactcctgac	88455
rs12312565	snp	A/G	0.124837	0.216412	intron-variant	ANKRD13A	GRCh38.p7	12:110011368	GGGATGGATGGAAGT[A/G]ACGCATGTGCACTTG	88455
rs12321161	snp	A/G	0	0	intron-variant	ANKRD13A	GRCh38.p7	12:110020780	ATGGGGAGGAACTGA[A/G]TGCCATCAGCAGGgc	88455
rs12425599	snp	C/G	0.110167	0.207236	intron-variant	ANKRD13A	GRCh38.p7	12:110029133	CTTTCCAAATAGAAT[C/G]TAGATTGGATGTAAG	88455
rs12810908	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110030861	gcactttgggaggcc[C/G]aggtgggtggatcac	88455
rs12824564	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110007653	cccaagtgctgggat[C/T]acaggtgtgagccac	88455
rs12825530	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110026224	cccacctcggcctcc[C/G]aaagtgctgagatta	88455
rs12826903	snp	A/C			intron-variant	ANKRD13A	GRCh38.p7	12:110026214	gtgatcctcacccac[A/C]tcggcctccgaaagt	88455
rs12826909	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13A	GRCh38.p7	12:110026216	gatcctcacccacct[C/T]ggcctccgaaagtgc	88455
rs12826919	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110026231	cggcctccgaaagtg[C/T]tgagattacaggcgt	88455
rs12827625	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110026234	cctccgaaagtgctg[A/G]gattacaggcgtgag	88455
rs28484840	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110001452	TTTTTTTTTTTTTTT[C/T]TTTTTGAGATGGAGT	88455
rs34060026	snp	C/T	9.8894e-05	0.00703116	synonymous-codon, intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110033903	GCAAGATGAAGATTA[C/T]GAGATAATGCAGTTT	88455
rs34137720	in-del	-/C			downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110039490	CTGGATGTACCCACA[-/C]CTTCCTGTTACGTAT	88455
rs34152716	in-del	-/A			intron-variant	ANKRD13A	GRCh38.p7	12:110033600	TTCGTTGTTTCCACT[-/A]AAAATCAAGGAAAAA	88455
rs34369572	in-del	-/C			intron-variant	ANKRD13A	GRCh38.p7	12:110003243	CTCTAGAGCCAGGCT[-/C]CCCTGTTTAGGAAGC	88455
rs34493523	snp	C/T	0.0114939	0.0749321	intron-variant	ANKRD13A	GRCh38.p7	12:110033056	GTTTTTTTCTTTTTC[C/T]TTTTTTTTTTTTTTT	88455
rs34501433	in-del	-/C			intron-variant	ANKRD13A	GRCh38.p7	12:110010476	AATGCAAGTTAGAGA[-/C]TAAGGTAAGAGAATC	88455
rs34586781	in-del	-/T			intron-variant	ANKRD13A	GRCh38.p7	12:110000755	TTCTTTCTTTCCTTC[-/T]TTTTTTTTTTTTTTT	88455
rs34589498	in-del	-/C			downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110039568	AGGTGGCATGCTCCT[-/C]CCCAGCCTTCCTGCC	88455
rs34796332	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110025248	GTAATCCCAGCTACT[C/T]TGGAGGCTGAGGCAC	88455
rs35012464	in-del	-/A	0.109814	0.206997	intron-variant	ANKRD13A	GRCh38.p7	12:110017932	GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAGT	88455
rs35040415	snp	C/G			intron-variant	ANKRD13A	GRCh38.p7	12:110011613	ATACTTCCTATTCTA[C/G]ACTTGAATGCTGATA	88455
rs35141236	in-del	-/G			intron-variant	ANKRD13A	GRCh38.p7	12:110012997	AGTCATGATCATCCT[-/G]GGTAAGGTTGGACTG	88455
rs35163441	in-del	-/A			intron-variant	ANKRD13A	GRCh38.p7	12:110009025	TCTGTAGGGATTTAT[-/A]CTTGTTCATCTAAGT	88455
rs35208482	in-del	-/C			upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997558	TTAAAGGGTTGCGAG[-/C]ATGAAAATGAAGAAG	88455
rs35224948	in-del	-/A			intron-variant	ANKRD13A	GRCh38.p7	12:110018811	TGGCATTGCTCACCC[-/A]AATGTTGTGCATACA	88455
rs35362218	in-del	-/C			intron-variant	ANKRD13A	GRCh38.p7	12:110006109	GCATGAGCCACTGCA[-/C]CCCAGCCCCATGTAT	88455
rs35367681	snp	C/T	0.153997	0.230832	intron-variant	ANKRD13A	GRCh38.p7	12:110037055	CGAGGATTCATTTTA[C/T]GAAGACTTATACTTA	88455
rs35432632	in-del	-/A	0.000327445	0.0127912	intron-variant	ANKRD13A	GRCh38.p7	12:110023965	CTTAAGCTGGGGGGG[-/A]AAAAAACTATAAAGG	88455
rs35473330	in-del	-/G			intron-variant	ANKRD13A	GRCh38.p7	12:110029003	GCCTCCCAAACTGCT[-/G]GGGATTACAGGCATG	88455
rs35525361	in-del	-/C			intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110034259	CTTCATCATTTTCTA[-/C]GCACTGAAGCAGTAT	88455
rs35606471	in-del	-/G			intron-variant	ANKRD13A	GRCh38.p7	12:110028347	CTTCCTGTGTAGTTT[-/G]GGTGATATCCTCATA	88455
rs35629888	in-del	-/C			intron-variant	ANKRD13A	GRCh38.p7	12:110028403	TAGTGAATAGAACTT[-/C]CCCGGTCTTTAGCTG	88455
rs35732772	in-del	-/A			upstream-variant-2KB	GIT2, ANKRD13A	GRCh38.p7	12:109997204	GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	88455
rs35891499	in-del	-/C			intron-variant	ANKRD13A	GRCh38.p7	12:110035066	TGGCCCCATTCCCAG[-/C]ACCCATTCAGTTTTC	88455
rs35945468	in-del	-/G			intron-variant	ANKRD13A	GRCh38.p7	12:110015688	GTAGCTAGGATTACA[-/G]GGCGTGTGCCACCAT	88455
rs36049730	in-del	-/G			intron-variant	ANKRD13A	GRCh38.p7	12:110029439	CTTTTCCCATCTGGT[-/G]GGAGATGACCTCAGT	88455
rs36087331	snp	C/T	0.000808934	0.0200951	synonymous-codon, intron-variant, downstream-variant-500B	ANKRD13A	GRCh38.p7	12:110033921	GATAATGCAGTTTGC[C/T]ATCCAGCAAAGTCTG	88455
rs55737380	snp	C/G	0.140242	0.224618	intron-variant	ANKRD13A	GRCh38.p7	12:110012787	AGGGATACTGTAGGC[C/G]AAGCCCTGCCTGCCA	88455
rs56249481	snp	A/G			intron-variant	ANKRD13A	GRCh38.p7	12:110019694	CGTGGAGTTTCTGGA[A/G]GTTAGAATTGACCCA	88455
rs56960173	snp	A/G	0.351635	0.228408	intron-variant	ANKRD13A	GRCh38.p7	12:110005654	TGGCATGTTTCAGGT[A/G]CTTAATTCCTTTTTA	88455
rs56972807	snp	A/G	0.349671	0.229272	intron-variant	ANKRD13A	GRCh38.p7	12:110036540	GGATCACGAGGTCAG[A/G]AGATTGAGACCATCC	88455
rs57109511	snp	C/T	0.00279162	0.0372561	intron-variant	ANKRD13A	GRCh38.p7	12:110003896	GGGCACGGTGGCTCA[C/T]GCCTGTACTCCCAGC	88455
rs57285442	snp	A/G	0.0275645	0.114116	intron-variant	ANKRD13A	GRCh38.p7	12:110009609	ACTCTTTATGCACTT[A/G]TTGTTTTAAAATCAC	88455
rs57307003	snp	C/T			intron-variant	ANKRD13A	GRCh38.p7	12:110030892	CTGAGGTCGGGAGTT[C/T]GAGACCAGCCTGACC	88455
rs57684892	snp	A/T			intron-variant	ANKRD13A	GRCh38.p7	12:110021740	CCCTCTCTCATTTTT[A/T]GATGGTCACTTTTCC	88455

Full records

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