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
rs346429183	snp	C/T			intron-variant	VCS	TAIR10	3:4306124	CTGCTAAGTTGCTAA[C/T]TCTGTCAGTGTTGGC	820530
rs346467936	snp	G/T			intron-variant	VCS	TAIR10	3:4309083	AACCATAAATCTTGT[G/T]TTTGTTTAGTGCATG	820530
rs346486482	snp	C/T			utr-variant-3-prime	VCS	TAIR10	3:4310135	TTGTTTTATATACGT[C/T]TACTATTCACTCTTC	820530
rs346509064	snp	G/T			intron-variant	VCS	TAIR10	3:4308570	TTAACGGAAAGGGAG[G/T]TTATCTCTTATATAT	820530
rs346535096	snp	A/G			intron-variant	VCS	TAIR10	3:4309158	TAGTTGAGGCGGTTA[A/G]CTAGAGAAGAGAACT	820530
rs346557328	snp	C/T			intron-variant	VCS	TAIR10	3:4305656	CGTTGCAAACTGGGT[C/T]TAATCCTGACATTTT	820530
rs346580050	snp	C/T			intron-variant	VCS	TAIR10	3:4307778	ACACACTACTAAACT[C/T]GTTGTTACCTTGATT	820530
rs346607310	snp	C/T			synonymous-codon	VCS	TAIR10	3:4305378	TAAACATGTACTGCG[C/T]ATTGATACTACAAAA	820530
rs346641411	snp	C/T			intron-variant	VCS	TAIR10	3:4305067	ACTTTGTGGTTTATA[C/T]CTCTATTTTTCTGTT	820530
rs346687868	snp	C/T			utr-variant-3-prime	VCS	TAIR10	3:4309977	CGTTCTCTCTTCTTG[C/T]TCGTTGCTTATATAA	820530
rs346699537	snp	C/G			missense, intron-variant	VCS	TAIR10	3:4304181	CCTTATCCGCCACCG[C/G]CGGCATCTTATCCTC	820530
rs346814607	snp	C/G			intron-variant	VCS	TAIR10	3:4307782	ACTACTAAACTTGTT[C/G]TTACCTTGATTTTGC	820530
rs346955040	snp	G/T			synonymous-codon	VCS	TAIR10	3:4304279	TCAACCATCTCCGGT[G/T]ACTCAGCAGCAACAG	820530
rs347006594	snp	A/C			missense, intron-variant	VCS	TAIR10	3:4304121	ACTAACCCTCACAAT[A/C]CTCCTCCGTTTGATC	820530
rs347017541	snp	A/C			synonymous-codon	VCS	TAIR10	3:4309883	CCGCAACGCACCGGG[A/C]AGCGATGTCTCAGCC	820530
rs347032689	snp	A/G			utr-variant-5-prime	VCS	TAIR10	3:4304081	TTAAATCTGCAAAAA[A/G]TCTATGGCGTCTTCT	820530
rs347067177	snp	C/T			missense	VCS	TAIR10	3:4306568	GCTTGCCACCACCTA[C/T]AGAAAATATGGGTTT	820530
rs347089827	snp	A/T			missense	VCS	TAIR10	3:4306793	CCAACGGTGAACCTA[A/T]AACTTCTGGCCTGCC	820530
rs347127521	snp	A/G			synonymous-codon, intron-variant	VCS	TAIR10	3:4304177	CAATCCTTATCCGCC[A/G]CCGGCGGCATCTTAT	820530
rs347146579	snp	C/G			intron-variant	VCS	TAIR10	3:4309121	TAGTTACTCTTGGTG[C/G]CTTTTCGCTGCTTAG	820530
rs347185614	snp	A/G			missense	VCS	TAIR10	3:4306802	AACCTAAAACTTCTG[A/G]CCTGCCATCTCAAAC	820530
rs347235994	snp	C/T			missense	VCS	TAIR10	3:4306748	TGAGTTTTCCATCAG[C/T]GGAAGCCACATCACA	820530
rs347239652	snp	A/T			utr-variant-3-prime	VCS	TAIR10	3:4310151	TACTATTCACTCTTC[A/T]TCACAAGAATATCTT	820530
rs347277240	snp	G/T			missense	VCS	TAIR10	3:4305954	CATCCAGTCAGTTCA[G/T]CCACGTTTGTGACAT	820530
rs347389621	snp	A/T			utr-variant-3-prime	VCS	TAIR10	3:4310114	TCTTTTAAATGTAAA[A/T]TCTGGTTGTTTTATA	820530
rs347425961	snp	A/T			missense	VCS	TAIR10	3:4307044	GAAGAAATCTCAAGA[A/T]GCAAGGACTCAAATG	820530

Full records

It may take some time, please wait.