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
rs1414368	snp	A/G	0.0601157	0.162616	synonymous-codon	ASB12	GRCh38.p7	X:64225579	CTCCTCCTCCTTGTC[A/G]GGCTGCAGGAGGGAG	142689
rs1414369	snp	A/G	0.388458	0.208157	intron-variant	ASB12	GRCh38.p7	X:64229564	ctgtgacaaactagc[A/G]aagtctgtaaacacc	142689
rs1414370	snp	A/C	0.389706	0.207322	intron-variant	ASB12	GRCh38.p7	X:64229875	TTGAAGGAAATAGTA[A/C]ATTTTAGTTAGAGGT	142689
rs1537764	snp	C/G	0.388208	0.208323	intron-variant	ASB12	GRCh38.p7	X:64226562	TGATTGCCAACACTG[C/G]CTCCCCATTCCTCTG	142689
rs5964744	snp	A/G	0.388458	0.208157	intron-variant	ASB12	GRCh38.p7	X:64229266	GAGTGGCAGAGGGAA[A/G]TGCTGAAGTTCTTGC	142689
rs6624673	snp	A/G	0.00211696	0.0324653	intron-variant	ASB12	GRCh38.p7	X:64229915	aaaaggtaattgtct[A/G]ttcatccaagtttct	142689
rs6653189	snp	C/G	0.17254	0.237697	upstream-variant-2KB	ASB12	GRCh38.p7	X:64232423	ATACAATCCACTTAT[C/G]TTATTTAAATCTCCC	142689
rs7058399	snp	A/G	0.389457	0.207489	intron-variant	ASB12	GRCh38.p7	X:64227364	ACCTTCCATTCACTT[A/G]TCCATTCTCTGCAGT	142689
rs9697943	snp	A/G	0.263729	0.249623	upstream-variant-2KB	ASB12	GRCh38.p7	X:64231392	caagtctttgctatt[A/G]tgaacagtgctgcag	142689
rs9698835	snp	A/G	0.389207	0.207657	upstream-variant-2KB	ASB12	GRCh38.p7	X:64231806	TGTGTCCAGCACTGG[A/G]AACTTTGTCAAAAAC	142689
rs12863067	snp	C/T			intron-variant	ASB12	GRCh38.p7	X:64230460	TAGGCTCCAGGTACT[C/T]ACCGGGCTTCAGCCT	142689
rs12863085	snp	C/T			utr-variant-5-prime	ASB12	GRCh38.p7	X:64230470	GTACTCACCGGGCTT[C/T]AGCCTGAGGCCATGC	142689
rs34077961	snp	A/G	0.0093982	0.0679027	missense	ASB12	GRCh38.p7	X:64225007	ACTGCACTGACCAGG[A/G]CCTATTGGCTCGTGT	142689
rs34588670	in-del	-/T			intron-variant	ASB12	GRCh38.p7	X:64228848	TTAACAAGAACTCAG[-/T]AACACACTTATAATC	142689
rs34689841	snp	A/G	0.000230345	0.0107294	synonymous-codon	ASB12	GRCh38.p7	X:64225384	CCACTTGAGCTGTTT[A/G]CAAGTCCTCTTAGCC	142689
rs34782767	snp	A/G	0.00316535	0.0396567	missense	ASB12	GRCh38.p7	X:64225551	GAGGACACTGACACA[A/G]AGGAGAAGCAGGCTC	142689
rs41298490	snp	G/T	0.00317376	0.039709	intron-variant	ASB12	GRCh38.p7	X:64224766	GATTGGCTTATACGT[G/T]ATTTAGAGCCCTGGG	142689
rs56884988	snp	A/G	0.172111	0.237557	upstream-variant-2KB	ASB12	GRCh38.p7	X:64232583	TTGCCTTTTATAGCC[A/G]TATCTACTTCCTTCC	142689
rs58669769	in-del	-/T	0.17254	0.237697	upstream-variant-2KB	ASB12	GRCh38.p7	X:64232230	GATGACAGAGTAAGG[-/T]GTTATTCTTGAAAAA	142689
rs73516486	snp	G/T	0.173397	0.237975	intron-variant	ASB12	GRCh38.p7	X:64224620	CAGAACCAGAAATTG[G/T]GCTAATGCTCCCCAC	142689
rs76596816	snp	C/T	0.000529661	0.016265	upstream-variant-2KB	ASB12	GRCh38.p7	X:64230953	ACTTTTTTTTTCTCT[C/T]TTTTTTTTTTCTAAT	142689
rs76758586	snp	C/T	0.0132126	0.0801981	upstream-variant-2KB	ASB12	GRCh38.p7	X:64230951	ACACTTTTTTTTTCT[C/T]TTTTTTTTTTTTCTA	142689
rs79631129	snp	C/T	0.5	0	upstream-variant-2KB	ASB12	GRCh38.p7	X:64230948	AGCACACTTTTTTTT[C/T]CTCTTTTTTTTTTTT	142689
rs111720709	in-del	-/T/TT	0.20649	0.252054	upstream-variant-2KB	ASB12	GRCh38.p7	X:64230951	CACTTTTTTTTTCTC[-/T/TT]TTTTTTTTTTTTCTA	142689
rs112515310	snp	C/T	0.0555816	0.157167	upstream-variant-2KB	ASB12	GRCh38.p7	X:64231113	TCCCACCTCCCCCCA[C/T]CCCACAACAGGCCCC	142689
rs138301074	snp	A/C/T	0.000351982	0.013262	missense	ASB12	GRCh38.p7	X:64225484	TTGTAACGCTCCTGG[A/C/T]GCAAAAGCTGGTCCA	142689
rs138334430	snp	A/G	0.000194536	0.00986053	synonymous-codon	ASB12	GRCh38.p7	X:64225225	GGCAGCTGTGAGCAC[A/G]GGAGAACAGTTGTTG	142689
rs138336167	snp	C/T	0.0168099	0.0901243	intron-variant	ASB12	GRCh38.p7	X:64227366	CTTCCATTCACTTGT[C/T]CATTCTCTGCAGTCT	142689
rs138886156	snp	A/G	0.0199298	0.0978146	upstream-variant-2KB	ASB12	GRCh38.p7	X:64231574	CATATCCTCCAACTC[A/G]TTGCCCCTCCCCTTC	142689
rs138954184	snp	A/G	0.00317376	0.039709	intron-variant	ASB12	GRCh38.p7	X:64226603	TTTTCCATCCTGTCT[A/G]ACCCAGGCTAGAGCC	142689
rs139142874	snp	A/G	0.000974121	0.0220479	missense	ASB12	GRCh38.p7	X:64225559	TTCTCCTCTGTGTCA[A/G]TGTCCTCCTCCTCCT	142689
rs139157259	snp	C/T	0.000323838	0.0127206	synonymous-codon	ASB12	GRCh38.p7	X:64224892	GTCAAGGGAGAGAGA[C/T]GGAAGGTAGATATTA	142689
rs139928365	snp	C/T	0.000297401	0.0121907	missense	ASB12	GRCh38.p7	X:64224365	TAGGTAGCTAATCAA[C/T]ATGGGAGGAATATCC	142689
rs140344771	snp	C/T	0.00370173	0.0428621	intron-variant	ASB12	GRCh38.p7	X:64227842	GACTCCTGTCAATGC[C/T]CTTGCCTCTTTATCC	142689
rs140412046	snp	C/T	0.00262306	0.0361199	intron-variant	ASB12	GRCh38.p7	X:64224502	GGTCATGAGGAGCAA[C/T]TATCAGCAAAATTCT	142689
rs140646521	snp	G/T	0.0199298	0.0978146	upstream-variant-2KB	ASB12	GRCh38.p7	X:64231736	CAGGCTCAGCCTGAA[G/T]AAAATGCCCACAACC	142689
rs140886394	snp	A/C	0.00158814	0.0281345	intron-variant	ASB12	GRCh38.p7	X:64229936	CCAAGTTTCTGGACC[A/C]CTTGAATTCTATCTA	142689
rs141298161	snp	A/C/T	0.0100156	0.0700533	intron-variant	ASB12	GRCh38.p7	X:64225935	AGCCTTCTCTAATCT[A/C/T]CTCTTCCTGCTCAGG	142689
rs141374514	snp	G/T	0.00954891	0.0684344	synonymous-codon	ASB12	GRCh38.p7	X:64224832	TCACCACTCACCTCG[G/T]GCCTGTAGCAGCAAT	142689
rs141503461	snp	G/T	0.000171551	0.00925992	synonymous-codon	ASB12	GRCh38.p7	X:64225369	AACATCAGCACCATG[G/T]GCTAAGAGGACTTGC	142689
rs142045870	snp	C/G	2.8327e-05	0.00376334	missense	ASB12	GRCh38.p7	X:64224830	GTTCACCACTCACCT[C/G]GGGCCTGTAGCAGCA	142689
rs142175292	snp	A/G	0.0245906	0.108123	intron-variant	ASB12	GRCh38.p7	X:64226884	CTCTTTGTTAGTCTG[A/G]GACCTCAGGTACCTA	142689
rs142712661	snp	C/T	0.0131573	0.0800346	upstream-variant-2KB	ASB12	GRCh38.p7	X:64232586	CCTTTTATAGCCATA[C/T]CTACTTCCTTCCTAC	142689
rs143070669	snp	G/T	0.000189982	0.00974449	missense	ASB12	GRCh38.p7	X:64225494	CCTGGCGCAAAAGCT[G/T]GTCCAAAGTATAGGA	142689
rs143874599	snp	C/T	0.00158814	0.0281345	intron-variant	ASB12	GRCh38.p7	X:64227666	TTAAGCGTCTCTATC[C/T]GAGCCCCCAGCTCTC	142689
rs143910837	snp	C/G	0.000425559	0.0145807	missense	ASB12	GRCh38.p7	X:64225263	TACCACCAGGAGAGG[C/G]ACCAGCTTCCAAAAG	142689
rs144066127	snp	A/C	0.0027524	0.0369949	missense	ASB12	GRCh38.p7	X:64224912	GGTAGATATTAGCAC[A/C]AAAATCGATTAACAG	142689
rs144295873	snp	A/C	0.00422943	0.0457911	intron-variant	ASB12	GRCh38.p7	X:64227949	GACCATTCTCATTGA[A/C]TATGCTTCATCTAGG	142689
rs144858124	snp	C/T	4.91105e-05	0.00495508	missense	ASB12	GRCh38.p7	X:64224438	CTGCGGACGACTAAA[C/T]GGACCTGTGATAGAA	142689
rs145043596	snp	C/T	0.0100156	0.0700533	upstream-variant-2KB	ASB12	GRCh38.p7	X:64231538	TCTCTTCTTTTTTCT[C/T]TTCTGAACTGAGCCT	142689
rs145078393	snp	A/G	0.00791544	0.0624105	intron-variant	ASB12	GRCh38.p7	X:64226140	GTTCAGAATGTGTGG[A/G]TTAGTAAGGTGGCTC	142689
rs145118752	snp	A/C/T	0.000515246	0.0160432	missense	ASB12	GRCh38.p7	X:64225418	TAAGAAGCAGCCAAG[A/C/T]GCAAGGGTGTCCCAG	142689
rs145600139	snp	A/G	0.00233562	0.0340933	synonymous-codon	ASB12	GRCh38.p7	X:64225042	GTCAGGGTCTGCCCC[A/G]TGGAGCAAAAGCAGG	142689
rs146485226	snp	A/G	2.37648e-05	0.00344701	missense	ASB12	GRCh38.p7	X:64224981	TTTCAAGGAGGGTGC[A/G]GGGTCTTGGGACACG	142689
rs146544947	snp	A/G	0.0147244	0.0845304	upstream-variant-2KB	ASB12	GRCh38.p7	X:64230750	GAGGGGCTCTCCCAT[A/G]GGGAAGTCCTGGAAG	142689
rs146601414	snp	A/G/T	0.000137733	0.00829758	missense	ASB12	GRCh38.p7	X:64225326	CAGCAGTGAAAAGTG[A/G/T]CGTCTGTGCCTTGAC	142689
rs147025022	snp	A/G	0.000598602	0.01729	synonymous-codon	ASB12	GRCh38.p7	X:64225153	TAGTTTAGCTTTGAC[A/G]TTGGCCTCTGCACCA	142689
rs147387213	snp	A/G/T	0.0142023	0.083063	intron-variant	ASB12	GRCh38.p7	X:64228437	TGGCAAAACATGGGA[A/G/T]TTCTGCTTCTACCCC	142689
rs148346736	snp	A/G	2.7789e-05	0.00372743	stop-gained	ASB12	GRCh38.p7	X:64225332	TGAAAAGTGGCGTCT[A/G]TGCCTTGACATCCAA	142689
rs148589525	snp	A/G	0.00042103	0.014503	missense	ASB12	GRCh38.p7	X:64224460	GTGATAGAAGTGACC[A/G]TGGAGTGGCTACAGC	142689
rs148909267	snp	C/T	0.00150785	0.0274163	missense	ASB12	GRCh38.p7	X:64225058	TGGAGCAAAAGCAGG[C/T]GGAAACAGTCCAGGT	142689
rs149424932	snp	C/T	0.00133517	0.0258032	missense	ASB12	GRCh38.p7	X:64224391	TATCCAGCTGGTTGA[C/T]GGCTTGTGGCTGGCC	142689
rs149446900	snp	C/T	0.0100156	0.0700533	intron-variant	ASB12	GRCh38.p7	X:64227407	ACACTCAAACATACA[C/T]CAAGAAAGCTCTTCA	142689
rs149758596	snp	C/G	0.0100156	0.0700533	upstream-variant-2KB	ASB12	GRCh38.p7	X:64230715	TACCAGTGCCATTCT[C/G]GGAGCGATTTCAGTA	142689
rs150163629	snp	C/T	0.000165467	0.00909429	missense	ASB12	GRCh38.p7	X:64225029	CAGTGCAGTTGTAGT[C/T]AGGGTCTGCCCCGTG	142689
rs150281410	snp	A/C	0.0121112	0.0768695	upstream-variant-2KB	ASB12	GRCh38.p7	X:64232534	ACCTTAGACAATATA[A/C]AGAATAGTTCTATCC	142689
rs150527136	snp	A/T	0.00370173	0.0428621	downstream-variant-500B	ASB12	GRCh38.p7	X:64223698	TCTCAGCCTATCACC[A/T]ATGTAACCAATTTAT	142689
rs151000379	snp	C/T	0.00528398	0.051128	intron-variant	ASB12	GRCh38.p7	X:64229935	TCCAAGTTTCTGGAC[C/T]CCTTGAATTCTATCT	142689
rs180733240	snp	C/T	0.000119989	0.00774468	missense	ASB12	GRCh38.p7	X:64225164	TGACGTTGGCCTCTG[C/T]ACCATGGTCTAGGAG	142689
rs181199270	snp	A/C/T	0.000215086	0.0103684	missense	ASB12	GRCh38.p7	X:64225578	CCTCCTCCTCCTTGT[A/C/T]GGGCTGCAGGAGGGA	142689
rs181421103	snp	C/T	0.000529661	0.016265	intron-variant	ASB12	GRCh38.p7	X:64229064	AACACAAACACATAC[C/T]CCCCTCCCTTGACTC	142689
rs181520639	snp	A/G	0.00105904	0.0229869	intron-variant	ASB12	GRCh38.p7	X:64229742	TCTAAGTGGTAATAA[A/G]TGACATTTCAAGATC	142689
rs181957184	snp	A/G	0.00317376	0.039709	intron-variant	ASB12	GRCh38.p7	X:64226115	AAATCTGGTAGATGC[A/G]TTTTCCTCAGTTCAG	142689
rs182359257	snp	C/T	0.000529661	0.016265	intron-variant	ASB12	GRCh38.p7	X:64230432	GCAGTGGTCACTCTT[C/T]TCAAACCGGTCCTAG	142689
rs182517924	snp	A/G			intron-variant	ASB12	GRCh38.p7	X:64227667	TAAGCGTCTCTATCC[A/G]AGCCCCCAGCTCTCT	142689
rs182555349	snp	A/G	0.142288	0.225606	upstream-variant-2KB	ASB12	GRCh38.p7	X:64230991	TAAGTTTTAGGGTAC[A/G]TGTGCACAACGTGCA	142689
rs182692758	snp	G/T	0.000529661	0.016265	intron-variant	ASB12	GRCh38.p7	X:64227181	TCATGAGGTTATTAG[G/T]AGTAAGAGAGCTACT	142689
rs183552866	snp	C/T			upstream-variant-2KB	ASB12	GRCh38.p7	X:64231774	ATCCTCACCCTAAAG[C/T]ATCACCATTACTTTA	142689
rs184012362	snp	A/C	0.00370173	0.0428621	intron-variant	ASB12	GRCh38.p7	X:64229128	CTTTTGAGTGTCATG[A/C]TGAATTCCAGGGTCT	142689
rs184030421	snp	C/T	0.00158814	0.0281345	upstream-variant-2KB	ASB12	GRCh38.p7	X:64232471	TTTTGTGTCTGTGTG[C/T]GTACATTTAATTCTA	142689
rs184462396	snp	A/G	0.000182896	0.0095611	intron-variant	ASB12	GRCh38.p7	X:64224810	GTGGCCTATGAGGCT[A/G]GCCTGTTCACCACTC	142689
rs184480877	snp	C/T	0.00105904	0.0229869	intron-variant	ASB12	GRCh38.p7	X:64228677	CTCCATTTTCTAAGG[C/T]TATTGCTCCCTACTT	142689
rs185743930	snp	C/T	0.00158814	0.0281345	intron-variant	ASB12	GRCh38.p7	X:64227911	CTACTAAAGACTTCT[C/T]CAGACCATCTGTGCT	142689
rs186146211	snp	G/T	0.00105904	0.0229869	upstream-variant-2KB	ASB12	GRCh38.p7	X:64230734	GCGATTTCAGTAAGA[G/T]GAGGGGCTCTCCCAT	142689
rs186241713	snp	C/T	0.000284172	0.0119166	utr-variant-5-prime	ASB12	GRCh38.p7	X:64225669	GAGCACAAGGAAATG[C/T]CAGATCTGTGGGTGA	142689
rs186887963	snp	A/G	0.000529661	0.016265	intron-variant	ASB12	GRCh38.p7	X:64230157	CAACACCACACAGGG[A/G]CACAAAGACAAATCT	142689
rs187371109	snp	C/T	0.000529661	0.016265	intron-variant	ASB12	GRCh38.p7	X:64227796	ATATCATTTCCTCAC[C/T]ATCTACCTGGTCAAC	142689
rs187808727	snp	A/G	0.00158814	0.0281345	intron-variant	ASB12	GRCh38.p7	X:64227280	TGTCCCACTCTAGCT[A/G]TCTTTCTCTTCGTCT	142689
rs188238209	snp	A/G			intron-variant	ASB12	GRCh38.p7	X:64228837	TTAGTTGTCTCATTA[A/G]CAAGAACTCAGAACA	142689
rs188588702	snp	A/T	0.00158814	0.0281345	upstream-variant-2KB	ASB12	GRCh38.p7	X:64231811	CCAGCACTGGAAACT[A/T]TGTCAAAAACTCAGC	142689
rs188659875	snp	A/G	0.00211696	0.0324653	intron-variant	ASB12	GRCh38.p7	X:64228108	TTAAATACCTTAATG[A/G]CTCCCCTTTCTTTCC	142689
rs189537672	snp	C/T	0.0173306	0.0914601	upstream-variant-2KB	ASB12	GRCh38.p7	X:64230816	TAGGGTTCCTGCTCC[C/T]AGCCTATCCTCCTAT	142689
rs190272829	snp	A/T	0.000529661	0.016265	intron-variant	ASB12	GRCh38.p7	X:64227431	CTCTTCAAAAGGTCA[A/T]CTTTGTGGTTAAATC	142689
rs190584854	snp	C/T	0.00422943	0.0457911	upstream-variant-2KB	ASB12	GRCh38.p7	X:64231128	CCCCACAACAGGCCC[C/T]GGTGTGTGATGTTCC	142689
rs190614396	snp	A/T	0.000529661	0.016265	intron-variant	ASB12	GRCh38.p7	X:64226029	TGTTCCATTAGTGTA[A/T]AAACTCCAGGGCAAG	142689
rs191124412	snp	C/T	0.00581083	0.0535878	intron-variant	ASB12	GRCh38.p7	X:64226812	CTACTCTCCCATACC[C/T]TGCAGCTGAGGTCTC	142689
rs191915614	snp	A/G	0.000529661	0.016265	intron-variant	ASB12	GRCh38.p7	X:64227859	TTGCCTCTTTATCCC[A/G]CTCTCATAAAATCCC	142689
rs192074016	snp	C/T	0.00370173	0.0428621	intron-variant	ASB12	GRCh38.p7	X:64230229	GCAGGTCTGTTTAGA[C/T]CCGAGGTCCTAGGCA	142689
rs193138421	snp	A/G	0.00158814	0.0281345	upstream-variant-2KB	ASB12	GRCh38.p7	X:64232307	AATTCACATGTGGTT[A/G]TGGAATTAATACAGA	142689
rs193229660	snp	C/T	0.000529661	0.016265	intron-variant	ASB12	GRCh38.p7	X:64228607	GTGCTTAGAATAGTG[C/T]CTGAAAGTAGTTCTC	142689

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