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
rs346455643	snp	C/T			intron-variant	?	TAIR10	2:158697	ACAAAAACCGCACTT[C/T]CAGGTTAGCGTTTAA	814661
rs346478006	snp	G/T			missense	?	TAIR10	2:158766	ATCACGTCACCTGTT[G/T]GGTCTCGCGATCCCA	814661
rs346482619	snp	A/C			missense	?	TAIR10	2:159072	AGACTAGTGCTGTGG[A/C]TTCGGGAGAATCAAC	814661
rs346498114	snp	A/G			synonymous-codon	?	TAIR10	2:158947	GTCTTGCCCTCCTAC[A/G]ATCGCTTCTTTCCCG	814661
rs346500052	snp	C/G			synonymous-codon	?	TAIR10	2:159831	GTGACCATCTTCTGA[C/G]GCCAATTCTCCAACT	814661
rs346524348	snp	A/G			missense	?	TAIR10	2:158439	GGTTCGATATGCCAC[A/G]AACGAACGGAAGCGT	814661
rs346556192	snp	C/T			synonymous-codon	?	TAIR10	2:158645	GCTGTTTATACGAGC[C/T]GTGTGGAACAACATG	814661
rs346560085	snp	A/G			synonymous-codon	?	TAIR10	2:158794	CCAGACTACAGCTTC[A/G]CGGTTGGCATCACCA	814661
rs346615518	snp	G/T			intron-variant	?	TAIR10	2:159185	CAAACCTGTCAAGAA[G/T]TGAAGATGTCATATG	814661
rs346622737	snp	A/G			intron-variant	?	TAIR10	2:159210	CATATGCGATGTAAC[A/G]TTGACTTTAACACAG	814661
rs346661506	snp	A/G			synonymous-codon	?	TAIR10	2:160702	GGAGATCAAAATGCC[A/G]CGGCCTCGTTCGGTG	814661
rs346664691	snp	A/C			missense	?	TAIR10	2:159873	CTTGCCATCGTAAAT[A/C]ATACCCTTTTTGTCA	814661
rs346672716	snp	A/G			synonymous-codon	?	TAIR10	2:158803	AGCTTCGCGGTTGGC[A/G]TCACCAGAAGCAAAC	814661
rs346680608	snp	C/T			intron-variant	?	TAIR10	2:160283	CATTAAAACCTAAAT[C/T]GTTTGCCTAATTACC	814661
rs346694205	snp	C/G			synonymous-codon	?	TAIR10	2:160480	TCTGAACTCGTTCTT[C/G]AGCACGAAGCCGTTG	814661
rs346717960	snp	A/G			utr-variant-5-prime	?	TAIR10	2:160839	TCTTCAGAGGAGGAG[A/G]AAGTTTAGGAGGAAA	814661
rs346811161	snp	C/T			missense	?	TAIR10	2:159310	TGAAAATGCTAGATT[C/T]AGTAGCCGCTAATCG	814661
rs346869885	snp	A/C			synonymous-codon	?	TAIR10	2:159819	GATACTGCCTTTGTG[A/C]CCATCTTCTGAGGCC	814661
rs346886162	snp	A/T			intron-variant	?	TAIR10	2:159207	TGTCATATGCGATGT[A/T]ACATTGACTTTAACA	814661
rs346913487	snp	C/T			missense	?	TAIR10	2:160596	CATAGCCATGTTCGC[C/T]GTAAACTTGGACGTC	814661
rs347097551	snp	C/T			missense	?	TAIR10	2:160449	ATTGGAGATCATCGA[C/T]ACGACCAGCAAGGAC	814661
rs347106773	snp	C/T			missense	?	TAIR10	2:158880	GTTTCTCCAGGACTG[C/T]TTCCTCTTTGAGGTT	814661
rs347128268	snp	C/T			missense	?	TAIR10	2:159637	TAATTACAGAGCCAA[C/T]AGTTCCATCTTCAGC	814661
rs347156690	snp	A/C			synonymous-codon	?	TAIR10	2:159079	TGCTGTGGCTTCGGG[A/C]GAATCAACGGCTATG	814661
rs347176806	snp	A/G			synonymous-codon	?	TAIR10	2:158980	AGGTGAGATCACAGA[A/G]GCTGCCACAGCAAAA	814661
rs347320012	snp	C/T			missense	?	TAIR10	2:158877	TGTGTTTCTCCAGGA[C/T]TGCTTCCTCTTTGAG	814661
rs347376079	snp	G/T			utr-variant-5-prime	?	TAIR10	2:160757	AGGAGTTTCGCCATC[G/T]TGGAATTGTTGGTAG	814661
rs347415550	snp	A/T			intron-variant	?	TAIR10	2:160298	TGTTTGCCTAATTAC[A/T]AAGGACTCGAAATTG	814661
rs347433964	snp	A/C			intron-variant	?	TAIR10	2:159743	ATTGCATAGCTTGGC[A/C]ACACATTGATATCCT	814661
rs347461768	snp	C/T			missense	?	TAIR10	2:158894	GCTTCCTCTTTGAGG[C/T]TGTTGTCCCCTGAGA	814661

Full records

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