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
rs346447929	snp	C/G			missense	?	TAIR10	2:10980226	CAGATCGAGCAGATT[C/G]GTGAGCTTGATTTCG	817117
rs346494987	snp	G/T			intron-variant	?	TAIR10	2:10980599	AGTAATCTCTGAATT[G/T]GCATTTGGTGGTGCT	817117
rs346536604	snp	A/T			intron-variant	?	TAIR10	2:10981812	TGATATGTAACATAC[A/T]ATTTTCGGTGATAAT	817117
rs346541244	snp	A/G			intron-variant	?	TAIR10	2:10980617	ATTTGGTGGTGCTTG[A/G]CAGTGGTAACCTCGG	817117
rs346616116	snp	A/T			intron-variant	?	TAIR10	2:10981082	CTCAAATATGTATGT[A/T]AGACATTGACACTGG	817117
rs346624476	snp	C/T			intron-variant	?	TAIR10	2:10981661	AAGTACTATGGACTC[C/T]TAAATTATTTGTGCA	817117
rs346645795	snp	C/T			missense	?	TAIR10	2:10982492	AGGCTGGCAAGTTTC[C/T]GGCAAAATACTGATC	817117
rs346672462	snp	A/C			missense	?	TAIR10	2:10980628	CTTGACAGTGGTAAC[A/C]TCGGTGATGATGAAC	817117
rs346710232	snp	A/C			synonymous-codon	?	TAIR10	2:10981138	TCTATTTCCTGAGGC[A/C]ACACTCCCCCTTAGA	817117
rs346711955	snp	A/C			synonymous-codon	?	TAIR10	2:10981144	TCCTGAGGCAACACT[A/C]CCCCTTAGAATCATT	817117
rs346728179	snp	C/T			synonymous-codon	?	TAIR10	2:10981922	GCATCGCTGGACTGA[C/T]GTTGAAGGATTTGTA	817117
rs346777522	snp	A/G			synonymous-codon	?	TAIR10	2:10983578	AAACAAGAAGTTGAA[A/G]CCATCGTCTTTTTGG	817117
rs346794761	snp	A/G			missense	?	TAIR10	2:10982531	TTCCGTATGACGCCA[A/G]GAGCATTTTGGCCAT	817117
rs346806872	snp	A/G			intron-variant	?	TAIR10	2:10981104	TGACACTGGTGCTTT[A/G]CAATACTTCAGGAGT	817117
rs346936787	snp	C/G			missense	?	TAIR10	2:10980231	CGAGCAGATTCGTGA[C/G]CTTGATTTCGAGGAA	817117
rs347035961	snp	A/G			intron-variant	?	TAIR10	2:10981987	GCATCTTTATTAGTA[A/G]AAATGGGGAATGCAT	817117
rs347103645	snp	A/C			missense	?	TAIR10	2:10983566	TTTCACAGCGACAAA[A/C]AAGAAGTTGAAGCCA	817117
rs347246525	snp	A/G			intron-variant	?	TAIR10	2:10980986	TTCTTCGGATTTGCA[A/G]GAAGTACTGTTTCTT	817117
rs347310399	snp	A/G			intron-variant	?	TAIR10	2:10980934	TGTTCACTGACATGG[A/G]ATGCTAACTTGAATT	817117
rs347321246	snp	A/G			missense	?	TAIR10	2:10982402	TTAGCTTCTAGCCAT[A/G]ACAACGAAAATGAAG	817117
rs347352883	snp	C/T			intron-variant	?	TAIR10	2:10981493	CTTTGTTTTGCTTTG[C/T]CTAATCTAAGACCTC	817117
rs347482212	snp	A/G			missense	?	TAIR10	2:10980178	AACTCGAGAGAAATG[A/G]ACGACGAGAGGATTC	817117

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