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
rs346426565	snp	G/T			synonymous-codon	ELP2	TAIR10	1:18333914	GAACGGTTCGAGCCG[G/T]AGAGCAAGAGCTGCT	841378
rs346434910	snp	A/G			missense	ELP2	TAIR10	1:18334030	CACTCTTCTCGTTGC[A/G]GTCTAGTCCAGTCCA	841378
rs346440137	snp	C/T			intron-variant	ELP2	TAIR10	1:18334353	GTGAAGTTGAAACCG[C/T]TTGAGTTACCTGTCC	841378
rs346483657	snp	C/G			intron-variant	ELP2	TAIR10	1:18334308	AACGTAGACATTTTT[C/G]GATGTTTTGAGAAAA	841378
rs346496508	snp	G/T			synonymous-codon	ELP2	TAIR10	1:18333874	GTCTCCAAGCTAACC[G/T]GTTCACAGCCGAGAC	841378
rs346522678	snp	G/T			missense	ELP2	TAIR10	1:18335401	AACCCTGACCTGATC[G/T]TGGCTCACGGATAGC	841378
rs346582696	snp	C/G			synonymous-codon	ELP2	TAIR10	1:18336447	AAAAGAAACATCCCA[C/G]ACATTCACAACTCCA	841378
rs346694539	snp	A/G			synonymous-codon	ELP2	TAIR10	1:18335494	TTTCTGCATCTGCCA[A/G]TTCTCAGACTCTTTG	841378
rs346760670	snp	A/G			synonymous-codon	ELP2	TAIR10	1:18334997	TAGGTTTCTGTGATA[A/G]TCCAAGAGCAGACAT	841378
rs346762228	snp	A/G			intron-variant	ELP2	TAIR10	1:18334899	TAGAAGCTGCGAAAA[A/G]AAATTAAGAATCTCA	841378
rs346775132	snp	C/T			missense	ELP2	TAIR10	1:18335574	CCAGAATAGACAGAC[C/T]ATTTGGGCTCCAATG	841378
rs346786604	snp	G/T			synonymous-codon	ELP2	TAIR10	1:18335923	ATCACCGACTAACAC[G/T]AGTTTCCAGATCCGA	841378
rs346787633	snp	A/T			synonymous-codon	ELP2	TAIR10	1:18335518	CTCTTTGCTGCTACT[A/T]ACATTTCTCCAGAGA	841378
rs346860922	snp	C/T			missense	ELP2	TAIR10	1:18335891	GCTAGAGTGATTTCT[C/T]TTCGCCACGAGCCAA	841378
rs346937169	snp	C/G			missense	ELP2	TAIR10	1:18335766	AATCGATGACTGGAG[C/G]TTGCCATTCCACAGA	841378
rs346937621	snp	C/T			missense	ELP2	TAIR10	1:18335738	TGGTGGTTAACTAGC[C/T]GCCCATCAATGAAAT	841378
rs347033810	snp	C/T			synonymous-codon	ELP2	TAIR10	1:18335719	CGATAAAATGCTCAG[C/T]GGTTGGTGGTTAACT	841378
rs347106221	snp	A/G			utr-variant-3-prime	ELP2	TAIR10	1:18333701	CAATGGTCCTGTATG[A/G]AAGAGAGTTTTGGAC	841378
rs347108781	snp	A/C			intron-variant	ELP2	TAIR10	1:18335359	TTGCATTATAATATA[A/C]TGAATCGTTTTAACA	841378
rs347114025	snp	C/T			intron-variant	ELP2	TAIR10	1:18336376	AGACATACTTCACTT[C/T]GTTTAACCGGTAATA	841378
rs347122307	snp	A/T			missense	ELP2	TAIR10	1:18336437	GCTGAGACGGAAAAG[A/T]AACATCCCAGACATT	841378
rs347170571	snp	C/G			missense	ELP2	TAIR10	1:18333861	CACTTCTCGGTTGGT[C/G]TCCAAGCTAACCTGT	841378
rs347191744	snp	C/G			intron-variant	ELP2	TAIR10	1:18336144	CACAAAAGCGAATCG[C/G]GAAGCACCTTTCCTG	841378
rs347380040	snp	C/T			utr-variant-3-prime	GGPS6, ELP2	TAIR10	1:18333656	TTAAACATGTTTCGA[C/T]TTAGCTAACCAAAAT	841378
rs347396635	snp	G/T			intron-variant	ELP2	TAIR10	1:18336868	AATGCCTATATCTTC[G/T]CAATTTGCTATCACT	841378
rs347408749	snp	C/G			missense	ELP2	TAIR10	1:18333972	ATAATCTTTACGTTC[C/G]ACAGCTCTATTAGCC	841378
rs347426613	snp	A/G			synonymous-codon	ELP2	TAIR10	1:18336013	GTGTAACGGTAATGA[A/G]AAGTCCAAACTCCGA	841378
rs347430410	snp	A/T			intron-variant	ELP2	TAIR10	1:18336353	AAAAGATGTAGATAC[A/T]GCTTAGAAGACATAC	841378
rs347461012	snp	A/C/G			missense, synonymous-codon	ELP2	TAIR10	1:18334025	GCACCCACTCTTCTC[A/C/G]TTGCGGTCTAGTCCA	841378
rs347483257	snp	G/T			synonymous-codon	ELP2	TAIR10	1:18336492	AGCAAACATTGCATC[G/T]GTTTCAGAAACCATA	841378

Full records

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