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
rs346464680	snp	A/T			intron-variant	?	TAIR10	1:7598695	AGCTTATCGAAATGA[A/T]CTGCATTACCTCACC	838767
rs346524571	snp	A/C			missense	?	TAIR10	1:7599443	CATACCATGAACGCC[A/C]TCACCAGTTAATGCA	838767
rs346588710	snp	C/T			synonymous-codon	?	TAIR10	1:7601450	AAACTAGTGGATTAC[C/T]TGTACATTGATGGTT	838767
rs346590305	snp	C/T			synonymous-codon	?	TAIR10	1:7599231	TTCAGCATCACGCTG[C/T]GCCAGGTAATCATTC	838767
rs346646710	snp	C/T			synonymous-codon	?	TAIR10	1:7599008	GAATGATATACTTAC[C/T]GAGTTATTGGTGTAT	838767
rs346660235	snp	A/T			missense	?	TAIR10	1:7602819	TTGAACCTAGGTTTC[A/T]TGACCAGCTCCCTGA	838767
rs346990747	snp	A/G			synonymous-codon	?	TAIR10	1:7603949	CAATCTGAGAAGATC[A/G]ATGTTTTTGGGGAGA	838767
rs346997081	snp	A/G			intron-variant	?	TAIR10	1:7594381	AATTAGTCACCCGAC[A/G]GCATCGTTTGGGAGT	838767
rs347023971	snp	A/G			intron-variant	?	TAIR10	1:7593126	AACAACAGATAATGA[A/G]CACTGTGCTTACCGC	838767
rs347086127	snp	C/T			intron-variant	?	TAIR10	1:7594559	AAGTAGTTGGAAAAG[C/T]TGGTACCTCTAGCAC	838767
rs347161420	snp	C/G			missense	?	TAIR10	1:7593210	TCTTTAAAAGAACTG[C/G]TCTCTATTTCCAAGA	838767
rs347175288	snp	A/T			missense	?	TAIR10	1:7592941	ATGACCAGTACTGCA[A/T]GATTGATTCTACGGT	838767
rs347197435	snp	C/G			intron-variant	?	TAIR10	1:7599762	ACACACACACACACA[C/G]ACACACACACACACG	838767
rs347235928	snp	A/C			synonymous-codon	?	TAIR10	1:7602632	TTCTGAGACTCTCCC[A/C]GGAAAATCTATGTCA	838767
rs347266241	snp	C/T			intron-variant	?	TAIR10	1:7596241	TCAGAAGTAGAGTTA[C/T]ACATCAAGGAGACAA	838767
rs347300606	snp	C/T			synonymous-codon	?	TAIR10	1:7603916	AGGTTCCAGCTTAAG[C/T]TTCGAAATCGAAGGG	838767
rs347335331	snp	C/T			intron-variant	?	TAIR10	1:7598245	ATAGTAATAAGTGGA[C/T]ACCTTGCCCATGGAT	838767
rs347345599	snp	C/T			synonymous-codon	?	TAIR10	1:7596315	TTGCCAATATACCTT[C/T]GGATTTCCTCCCAGA	838767
rs347349045	snp	A/T			missense	?	TAIR10	1:7593552	GATATCAAGCCAACG[A/T]CTTAGTGAAGAATTC	838767
rs347377289	snp	A/T			missense	?	TAIR10	1:7593633	GGACAAGTCTTCCAT[A/T]TCTATTGAACTTCCC	838767
rs347384789	snp	C/T			intron-variant	?	TAIR10	1:7596146	TGAAAGATTAAGCCA[C/T]AAACATAGCAGGTTA	838767
rs347409376	snp	A/G			intron-variant	?	TAIR10	1:7599767	CACACACACACACAC[A/G]CACACACACGCACAA	838767
rs347412030	snp	A/G			missense	?	TAIR10	1:7595107	TTCCAGCTCTGCCAC[A/G]AAGCTATAAGAAATA	838767
rs347460465	snp	A/G			intron-variant	?	TAIR10	1:7596462	ATATTAGAACTAGCT[A/G]AAAATAATGCTATGT	838767

Full records

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