iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

At2g47410

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs346444583	snp	C/T			intron-variant	?	TAIR10	2:19453386	ATCAATTTTTTAAGA[C/T]ACTATTTCCCTGGCA	819354
rs346460144	snp	G/T			intron-variant	?	TAIR10	2:19453743	GACCTCACCGAACTG[G/T]GCATACTTTTTATAT	819354
rs346460701	snp	A/C			utr-variant-5-prime	?	TAIR10	2:19448567	TTGAAAAATCGTCTA[A/C]TCGAGATTCCTTTCT	819354
rs346503848	snp	C/T			intron-variant	?	TAIR10	2:19453396	TAAGATACTATTTCC[C/T]TGGCACTGTGTAGAG	819354
rs346544359	snp	A/C			utr-variant-3-prime	?	TAIR10	2:19457040	CTTTCTTGATCTTGT[A/C]AACACGTTAGGCTGC	819354
rs346545051	snp	C/G			intron-variant	?	TAIR10	2:19455776	ACGTCCTCTTGGCTG[C/G]TAATTCGTTGTTCAC	819354
rs346564771	snp	A/C			intron-variant	?	TAIR10	2:19455813	GTATTAATTTGCCAG[A/C]TGTGATATTAATAAA	819354
rs346603925	snp	A/G			intron-variant	?	TAIR10	2:19453769	TATATCCTTGCACCT[A/G]CGGTATTTTTGAATA	819354
rs346638594	snp	C/G			intron-variant	?	TAIR10	2:19448688	TTGTCTTTTCTAGCT[C/G]CCGAATTTGCCAGTT	819354
rs346657088	snp	C/G			intron-variant	?	TAIR10	2:19456745	TGTGGATTTTCTTAT[C/G]TGGCAGTAATGATTC	819354
rs346673670	snp	A/G			intron-variant	?	TAIR10	2:19450565	GGAACTCTATACTTT[A/G]TTTTGTTACATGTGC	819354
rs346687566	snp	A/G			missense	?	TAIR10	2:19454816	AGGGAGATGTGATAA[A/G]TCAGGCTGATTTAGA	819354
rs346697112	snp	A/T			missense	?	TAIR10	2:19455543	CAAGGGATTCCTTCC[A/T]CAAGCGTGTATGATG	819354
rs346699797	snp	A/G			synonymous-codon	?	TAIR10	2:19454577	GCCGCAGAGAGCAGC[A/G]GCTCAAAATGCTCGA	819354
rs346743131	snp	A/G			missense	?	TAIR10	2:19455262	ATCCCAACAGTCCTC[A/G]AAAACTAGAACCTGA	819354
rs346749873	snp	C/T			synonymous-codon	?	TAIR10	2:19456172	TGTGTGGTGGAGAGA[C/T]GCAACCGGTGAAGGC	819354
rs346804181	snp	A/C			intron-variant	?	TAIR10	2:19449896	TGAATTGATGTTTGG[A/C]AATCAGGATATGTTT	819354
rs346821343	snp	A/G			synonymous-codon	?	TAIR10	2:19456799	AAATCGCAGGTTCCC[A/G]GTTCCATTATACCCT	819354
rs346825100	snp	C/G			missense	?	TAIR10	2:19456921	TGTATTTCGTTAGAA[C/G]TGCACATATGCTTTC	819354
rs346830271	snp	C/T			intron-variant	?	TAIR10	2:19449555	ATGTGCTGTTACTTG[C/T]CTCTCAACATGTGTC	819354
rs346894659	snp	C/T			intron-variant	?	TAIR10	2:19454383	ATGCGATTTTGTTTG[C/T]CAGTATCTATTAACT	819354
rs346896470	snp	C/T			intron-variant	?	TAIR10	2:19451860	TGTGCAATTTAGGTA[C/T]TTTCCAGCGAACGTG	819354
rs346913935	snp	A/G			utr-variant-3-prime	?	TAIR10	2:19457218	ACTCTGTTGTCACAA[A/G]AATGACATCATAAGT	819354
rs346947704	snp	G/T			missense	?	TAIR10	2:19456951	CGAAGATAAAGCGAC[G/T]GCGAGATAAATTGAC	819354
rs347047113	snp	C/T			intron-variant	?	TAIR10	2:19453044	GGAATAGTCCTTAAT[C/T]TTATCAATAGCGATA	819354
rs347054779	snp	G/T			intron-variant	?	TAIR10	2:19451044	CTTTAATGTCTTACT[G/T]GTTTTTATTTATTTG	819354
rs347084205	snp	C/T			missense	?	TAIR10	2:19452193	CAAGATCACGTAAAT[C/T]CCATGTAAGTTCTGT	819354
rs347118632	snp	A/G			intron-variant	?	TAIR10	2:19456710	TCGGTGCTTATTTAA[A/G]TAACTCATATGATCA	819354
rs347135633	snp	C/T			intron-variant	?	TAIR10	2:19450189	AACTTGGATAGTCTC[C/T]CTAACCTCTCCAATT	819354
rs347135634	snp	C/G			synonymous-codon	?	TAIR10	2:19456952	GAAGATAAAGCGACT[C/G]CGAGATAAATTGACA	819354
rs347140923	snp	A/G			intron-variant	?	TAIR10	2:19451511	GTTTCTCTCTTAGGC[A/G]AAAGCACTTTTACAT	819354
rs347150458	snp	G/T			intron-variant	?	TAIR10	2:19450674	GAGCACCGTTTATTG[G/T]CATAGAATGTTTTTT	819354
rs347170174	snp	G/T			intron-variant	?	TAIR10	2:19449996	TCAGCAACATGTTCC[G/T]TTGGATCTGGGACTT	819354
rs347226072	snp	G/T			intron-variant	?	TAIR10	2:19449074	GCATGCTTTAATTGA[G/T]GAGACTGTCTTTCAC	819354
rs347274524	snp	A/G			utr-variant-5-prime	?	TAIR10	2:19448358	ATCTCACAGCGGTAA[A/G]AAAAAAAGAAAAAGA	819354
rs347329056	snp	A/G			intron-variant	?	TAIR10	2:19453297	CATATCCAATTGGGT[A/G]TACAATATTCATATT	819354
rs347333689	snp	A/G			missense	?	TAIR10	2:19454419	CCGTTTTCTCAGGTC[A/G]ACGTCTCTACTTCAT	819354
rs347348287	snp	C/G			intron-variant	?	TAIR10	2:19452219	TCTGTCAATCAATCA[C/G]TGAATGCAATGTGCA	819354
rs347396497	snp	G/T			utr-variant-5-prime	?	TAIR10	2:19449117	ATTTTTTTGACGAGT[G/T]CTTCTCTTCCTTATC	819354
rs347398547	snp	C/T			intron-variant	?	TAIR10	2:19453365	TAGTCACATGAAAGT[C/T]TTGGAATCAATTTTT	819354
rs347415840	snp	C/G			intron-variant	?	TAIR10	2:19453236	ACTCCAGTTAAACAT[C/G]CAATTGACTATTGAG	819354
rs347472083	snp	C/T			missense	?	TAIR10	2:19455337	CCATAGCTCCCTCTT[C/T]CATGAATCCGATTAT	819354
rs347478726	snp	C/T			intron-variant	?	TAIR10	2:19451290	GTTTCATACTGCGTC[C/T]GGATTGGTAATCAGT	819354