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
rs346432404	snp	A/G			missense	?	TAIR10	2:19118128	GAGTTTTCATTGGCA[A/G]TTACCGCAGCTTTTG	819268
rs346437461	snp	C/T			synonymous-codon	?	TAIR10	2:19122102	CCCTGACTGAAACTG[C/T]GAATACTGTAGCATT	819268
rs346446438	snp	C/T			intron-variant	?	TAIR10	2:19121250	TATTAGTACATGGGT[C/T]CTTGCATAGCTAGTG	819268
rs346519674	snp	C/T			synonymous-codon	?	TAIR10	2:19124394	TTCTTGTTTCGCCCA[C/T]AATGTTACTCGTGGA	819268
rs346524657	snp	C/T			missense	?	TAIR10	2:19120307	CCAATGCGTTCTTCA[C/T]ACTATTTTTGGTTGC	819268
rs346554486	snp	A/C			missense	?	TAIR10	2:19124018	TCAAATAAACACTAG[A/C]GGAGCAGATTATTAT	819268
rs346573893	snp	C/T			missense	?	TAIR10	2:19119834	GACCGTTACTTGGAA[C/T]GCTAGTCTGATGGGT	819268
rs346583484	snp	G/T			intron-variant	?	TAIR10	2:19121145	CATCAAAATAAGTGA[G/T]GCACATCTATTTTCT	819268
rs346619050	snp	C/G			missense	?	TAIR10	2:19117306	TAAAAAATGATCCTG[C/G]ATCCGCTATCGCTCC	819268
rs346619338	snp	C/G			missense	?	TAIR10	2:19118927	GGTCAACCTCATAAG[C/G]CATATGCCCATTAAA	819268
rs346663830	snp	C/G			missense	?	TAIR10	2:19118926	AGGTCAACCTCATAA[C/G]GCATATGCCCATTAA	819268
rs346678041	snp	A/G			intron-variant	?	TAIR10	2:19120121	AGCTTTCAACATGGT[A/G]CCTTGGTAAAAACAT	819268
rs346720246	snp	C/T			intron-variant	?	TAIR10	2:19125775	ACTATTTTTTTCCGA[C/T]TGTGCTACACAACTT	819268
rs346742240	snp	A/G			missense	?	TAIR10	2:19125799	ACAACTTACCAGTAC[A/G]AGGATCACCGGACCC	819268
rs346752745	snp	A/G			missense	?	TAIR10	2:19122715	ATATCATTAGTACCA[A/G]AATCAGATAAGAATT	819268
rs346793080	snp	C/T			missense	?	TAIR10	2:19120418	GGTTCTCTAGACACC[C/T]AGCCATAGCAAGAAT	819268
rs346801193	snp	A/T			synonymous-codon	?	TAIR10	2:19121301	AAAACTTACCCGTGA[A/T]CGCAATTGTGCTGCA	819268
rs346825696	snp	A/G			missense	?	TAIR10	2:19122092	TTGACTGCAACCCTG[A/G]CTGAAACTGCGAATA	819268
rs346869383	snp	C/G			intron-variant	?	TAIR10	2:19125704	GTGAGATCGCGACGT[C/G]ACTCGTCTCCGGCAT	819268
rs346877140	snp	A/G			synonymous-codon	?	TAIR10	2:19115621	GACGAACTTCACCGT[A/G]CCATCACCACCACAC	819268
rs346887111	snp	A/G			missense	?	TAIR10	2:19120403	AGCTCTCAGTAGCAG[A/G]GTTCTCTAGACACCC	819268
rs346907234	snp	A/T			missense	?	TAIR10	2:19121962	GCAAAATATTGCAAT[A/T]TTTCTATCCTGGAAA	819268
rs346922123	snp	C/T			synonymous-codon	?	TAIR10	2:19125087	TCCACCAACTATTAT[C/T]CCATCCCCGGATCCT	819268
rs346932528	snp	A/G			synonymous-codon	?	TAIR10	2:19115878	TGTGTCTTTCGTGTA[A/G]TTTAGGCCAATGATG	819268
rs346953527	snp	A/G			synonymous-codon	?	TAIR10	2:19122918	ATCATGTATAGCCGA[A/G]AATGTACGAGTAACA	819268
rs346989497	snp	A/G			missense	?	TAIR10	2:19124458	ACAGCCCACAAAGTA[A/G]CAAAATTTCCAGGGC	819268
rs347011926	snp	A/G			intron-variant	?	TAIR10	2:19119961	CCAAACTCAATCTCA[A/G]AAAAAAAAAAAAAAA	819268
rs347032490	snp	A/T			intron-variant	?	TAIR10	2:19119511	AACTGAGAAAACTAA[A/T]ATGATGTGCAAGCAG	819268
rs347060245	snp	C/T			missense	?	TAIR10	2:19123180	CATATACTAACTGCG[C/T]GGGCAGCTTTTGAAT	819268
rs347067174	snp	C/T			missense	?	TAIR10	2:19124447	CAAGACAATGGACAG[C/T]CCACAAAGTAGCAAA	819268
rs347109965	snp	A/T			missense	?	TAIR10	2:19124887	GATTCACCATCACTA[A/T]AATAGGCCAAGACAC	819268
rs347115136	snp	A/T			missense	?	TAIR10	2:19118331	GAAAGCTTCGTGTAG[A/T]AAATGAGGATCAACA	819268
rs347195226	snp	A/G			missense	?	TAIR10	2:19123639	ACACTCCATGACAGA[A/G]CATCAAACCGTTTCT	819268
rs347206874	snp	A/G			synonymous-codon	?	TAIR10	2:19115825	TTCACTAACCCGGAT[A/G]ATTCCACCGTAGCCT	819268
rs347249203	snp	C/G			missense	?	TAIR10	2:19125676	GGCAAATGATCGATC[C/G]GATCTGTGACCAGTG	819268
rs347254811	snp	C/T			missense	?	TAIR10	2:19125577	GCAAGCCATGAGTAA[C/T]TAGCGAAGTCGGGAA	819268
rs347271648	snp	A/G			missense	?	TAIR10	2:19118368	TTCCAGAACCTCACA[A/G]AAACCACAGGGTCAC	819268
rs347343261	snp	C/T			missense	?	TAIR10	2:19125578	CAAGCCATGAGTAAT[C/T]AGCGAAGTCGGGAAG	819268
rs347370504	snp	A/G			intron-variant	?	TAIR10	2:19118056	AATGTAAGAAAAATA[A/G]GTACCTCTATAAGCT	819268
rs347375210	snp	A/G			intron-variant	?	TAIR10	2:19119973	TCAGAAAAAAAAAAA[A/G]AAAAAAAAAAACATC	819268
rs347398358	snp	A/G			intron-variant	?	TAIR10	2:19116080	AAAATAGGCTTTAGG[A/G]TGTGCACCTAAGTGA	819268
rs347422191	snp	A/G			intron-variant	?	TAIR10	2:19125339	AATAACAAGGAAGAT[A/G]TATCGAGGCTTACCT	819268
rs347428381	snp	C/G			missense	?	TAIR10	2:19124815	TGTTCTGCAGCCATC[C/G]GTCTCCACTGAATCA	819268
rs347445921	snp	C/T			missense	?	TAIR10	2:19124842	ATCATGGATATTCTC[C/T]GAGGATGAGGCAATT	819268
rs347457953	snp	A/C			missense	?	TAIR10	2:19116856	TGCTGATATCGACGC[A/C]AAAGCATAAGGAGGG	819268

Full records

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