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
rs346479926	snp	C/T			synonymous-codon	?	TAIR10	2:18898101	AAGAGCGTGGCTGGA[C/T]AGTGAGCATGATACT	819199
rs346520286	snp	A/G			missense	?	TAIR10	2:18896579	GAGAGCCAGATAGCA[A/G]AATCTGATGGTACAA	819199
rs346595328	snp	A/G			synonymous-codon	?	TAIR10	2:18894618	GTCTAGTAGGAGCGG[A/G]ATTATGGACGAACCT	819199
rs346692644	snp	A/G			synonymous-codon	?	TAIR10	2:18896881	TCAGGTGGCTATAAA[A/G]ATGTTGAATCCTAAC	819199
rs346703166	snp	G/T			intron-variant	?	TAIR10	2:18895270	CTTATGGCGAGTCAC[G/T]AAGCATTTTTTGGGA	819199
rs346740097	snp	A/G			missense	?	TAIR10	2:18896718	AGGAGTTAAGGAGTC[A/G]CGCAGAAACCTCAAC	819199
rs346820897	snp	G/T			intron-variant	?	TAIR10	2:18895282	CACTAAGCATTTTTT[G/T]GGATCTCTACTTATT	819199
rs346839436	snp	A/C			missense	?	TAIR10	2:18896547	TTCAAAGTGCAATGG[A/C]TCAGAAAGCGATGCT	819199
rs346898113	snp	A/T			synonymous-codon	?	TAIR10	2:18895426	GAAAGCCATCTTCGT[A/T]CGCCGAGAAGCACCT	819199
rs346976827	snp	C/T			synonymous-codon	?	TAIR10	2:18897457	AAGTGTGAGAACTGA[C/T]GTTACAGGCACAGTT	819199
rs346988391	snp	A/G			synonymous-codon	?	TAIR10	2:18896518	AAACGAGCAAGAGGT[A/G]ATCATGGAAGAACTT	819199
rs347003866	snp	A/G			intron-variant	?	TAIR10	2:18895379	TCTATCAATACTTTG[A/G]CTTTCAGGAGAATGA	819199
rs347155969	snp	C/T			synonymous-codon	?	TAIR10	2:18897295	TGCCACTGAGATATG[C/T]GCAGCACTTGTCTTT	819199
rs347164265	snp	C/T			synonymous-codon	?	TAIR10	2:18897509	TCCAGTAGTGGAGAG[C/T]TAACTCCTAAGTCAG	819199
rs347224533	snp	G/T			missense	?	TAIR10	2:18897308	TGTGCAGCACTTGTC[G/T]TTCTTCATTCTAATA	819199
rs347233453	snp	G/T			intron-variant	?	TAIR10	2:18897097	GGAGCTTTGACTTAT[G/T]CTTGCGGCATTGCAG	819199
rs347323022	snp	A/G			synonymous-codon	?	TAIR10	2:18897691	GCAGCTTGCTCGCTT[A/G]GCATTGAGATGCTGC	819199
rs347347358	snp	A/G			missense	?	TAIR10	2:18897582	GGAGACCTGCCTTAC[A/G]GATATCAAATGAAGT	819199
rs347378075	snp	A/T			missense	?	TAIR10	2:18897389	GATTCCAATCTCGTT[A/T]GCAAGTTAAGTGACT	819199
rs347431282	snp	C/G			missense	?	TAIR10	2:18897520	AGAGCTAACTCCTAA[C/G]TCAGATGTTTACTCG	819199
rs347453786	snp	C/T			intron-variant	?	TAIR10	2:18897934	TCGATCACAAAGTCA[C/T]TAAAATTTGCTTATC	819199

Full records

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