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

At1g52360

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs346466516	snp	A/G			intron-variant	?	TAIR10	1:19504485	TATGCACCTTTGGTT[A/G]ACTGTGTGACAATAT	841666
rs346467504	snp	C/G			synonymous-codon	?	TAIR10	1:19500243	AAAATCCTTTGAGGT[C/G]ACTGAATTACCAGGT	841666
rs346473775	snp	C/T			intron-variant	?	TAIR10	1:19504675	TGGGTTTAAGTTACC[C/T]TGCACTTGAATACAG	841666
rs346518776	snp	A/G			missense	?	TAIR10	1:19500392	CGGTCAGCCAAGTTT[A/G]TAGCACGAAAGCAAT	841666
rs346546398	snp	C/T			intron-variant, missense	?	TAIR10	1:19499471	TTTGCCTGCCGATGG[C/T]GTGAATTCGAGTGTA	841666
rs346547772	snp	A/G			intron-variant	?	TAIR10	1:19500745	ATTATGGTTTAGTCC[A/G]CTTAGTCCGCTCATT	841666
rs346595279	snp	C/T			intron-variant	?	TAIR10	1:19502906	AATTTCTATATGCGA[C/T]TCATGGATTGTCCAA	841666
rs346598490	snp	A/C/T			intron-variant	?	TAIR10	1:19500744	CATTATGGTTTAGTC[A/C/T]GCTTAGTCCGCTCAT	841666
rs346682733	snp	A/T			intron-variant	?	TAIR10	1:19504149	GGGAGCAACAGCAAA[A/T]TCTCTGTTTCTCGTC	841666
rs346738916	snp	G/T			utr-variant-3-prime	?	TAIR10	1:19505837	TGGAACCACATTTTG[G/T]AACCATTTTGTAATA	841666
rs346775272	snp	A/T			intron-variant	?	TAIR10	1:19503200	TGATGGTTGCTAACA[A/T]CGTAATACTAGGTAA	841666
rs346840782	snp	C/T			synonymous-codon	?	TAIR10	1:19502205	GAGGTTTGTCGTAGT[C/T]TGTGGTGACGGAGAA	841666
rs346841843	snp	G/T			intron-variant, missense	?	TAIR10	1:19499435	ATGTTTCTCTTCGAC[G/T]TGTCTAATCTGATTC	841666
rs346862592	snp	A/T			utr-variant-5-prime	?	TAIR10	1:19499255	TCCCAAGGGGCTCAC[A/T]AGCCTTTCTACGCTT	841666
rs346909715	snp	A/T			intron-variant	?	TAIR10	1:19504215	AACTCTTTCCGTTTT[A/T]ATGTCATCATGACAG	841666
rs346933870	snp	A/C			intron-variant	?	TAIR10	1:19505548	GCAACCCTTAGGAAC[A/C]TAACACCAATTTTGT	841666
rs346973934	snp	A/C			intron-variant	?	TAIR10	1:19505098	GATCACGAGGTGACC[A/C]ATTTTCTTTTCCAAT	841666
rs346976158	snp	G/T			intron-variant	?	TAIR10	1:19502373	TTCTAAATCTTTTTC[G/T]CTCTGATCTAAGCCG	841666
rs346976735	snp	C/T			intron-variant	?	TAIR10	1:19505612	AGTATACATGCTTCA[C/T]CTTCTTATATAAACT	841666
rs346997136	snp	C/G			intron-variant	?	TAIR10	1:19502055	ATTTTCTGCGTTGCT[C/G]GTATGATTGGCAAGT	841666
rs347005114	snp	C/T			intron-variant	?	TAIR10	1:19504829	TTTTGCTCAAGTGTG[C/T]TTTTCTCTTCCATGG	841666
rs347051103	snp	C/G			intron-variant	?	TAIR10	1:19502031	TTATATAGTTCATTT[C/G]GGAAAAACATTTTCT	841666
rs347077621	snp	G/T			missense	?	TAIR10	1:19505008	AGCCATGCTGATAAA[G/T]CTTCCATGACCCTCG	841666
rs347082562	snp	A/G/T			intron-variant	?	TAIR10	1:19505643	AACAGTGTCTCGGGG[A/G/T]TTTATTGGTTGCTGA	841666
rs347204507	snp	C/T			intron-variant, utr-variant-5-prime	?	TAIR10	1:19499410	GTGAGACCTTGGAAT[C/T]TCAGATCGCATGTTT	841666
rs347240297	snp	C/T			intron-variant	?	TAIR10	1:19503180	TGTTATGAACTGGAT[C/T]CTAATGATGGTTGCT	841666
rs347248276	snp	A/T			intron-variant	?	TAIR10	1:19503734	TTCGGACAATTTTCG[A/T]CTTGTTAGTGTTGCT	841666
rs347274703	snp	C/G			intron-variant	?	TAIR10	1:19501613	ACTCCATTGAGTTGT[C/G]CTGCAAAACCTTACC	841666
rs347286956	snp	C/G			intron-variant	?	TAIR10	1:19501435	TTAGTTTTTGGCTCC[C/G]TTCTCTTATTAATAA	841666
rs347338765	snp	C/T			utr-variant-3-prime	?	TAIR10	1:19505985	TTTTTGTCTTTTGCA[C/T]TCACAGGGAGGTTTA	841666
rs347360267	snp	G/T			intron-variant	?	TAIR10	1:19504930	CGACATTCTCAGACC[G/T]CTCTTTAAAATTGTC	841666
rs347365342	snp	C/G			intron-variant	?	TAIR10	1:19501990	CTACAGCACTCGGTC[C/G]AATGATTTTATGATG	841666
rs347384520	snp	C/T			utr-variant-3-prime	?	TAIR10	1:19505914	CTTTGCTGGAGAGAC[C/T]GGAAGATTTAGATGA	841666
rs347393217	snp	C/T			intron-variant	?	TAIR10	1:19501256	CCACTTTGGCTTCAT[C/T]CTTGTGCACTTTTTC	841666
rs347393493	snp	C/G			intron-variant	?	TAIR10	1:19504878	AATCGTTAATACCTA[C/G]TGCATCCACGTAGTG	841666
rs347469531	snp	A/G			intron-variant	?	TAIR10	1:19501809	GATTACGAGGTACAC[A/G]CCATACTTGTAACTC	841666