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
rs346424358	snp	A/C			missense	?	TAIR10	1:6422777	CTCTCAGGTCTACAG[A/C]TTGATCCCTTTAGGT	838447
rs346431149	snp	A/G			synonymous-codon	?	TAIR10	1:6421703	GGTTTTTCAACTTGT[A/G]GAGAAGGGAAACCAA	838447
rs346445693	snp	C/T			utr-variant-3-prime	?	TAIR10	1:6425872	GTTAGTTAATTTTGG[C/T]ACTGTTTTATCAAAT	838447
rs346465944	snp	A/G			intron-variant	?	TAIR10	1:6422005	TAGAATATTCTGCAA[A/G]TTCGTGCTAGTTTAA	838447
rs346476015	snp	G/T			synonymous-codon	?	TAIR10	1:6423985	GGTAGCTCTTGATTC[G/T]GCGACAGGTTCTCCA	838447
rs346508560	snp	A/C			intron-variant	?	TAIR10	1:6421864	ATGATAAATAGTCTT[A/C]GGTCCTTCAATAAAA	838447
rs346528341	snp	C/G			missense	?	TAIR10	1:6424812	GGGAACTGACGACCA[C/G]CGCAGCATCATTTGC	838447
rs346553590	snp	C/G			utr-variant-3-prime	?	TAIR10	1:6425691	ATAGAGATCCTTGTA[C/G]GATCGCTGTCATCCT	838447
rs346571881	snp	A/T			intron-variant	?	TAIR10	1:6423523	TGAGTTCTTTCAAAA[A/T]TTTTCGGTTATGTAC	838447
rs346574778	snp	A/T			utr-variant-3-prime	?	TAIR10	1:6425873	TTAGTTAATTTTGGC[A/T]CTGTTTTATCAAATC	838447
rs346579592	snp	A/G			missense	?	TAIR10	1:6422885	TGATCGCATGAAGCG[A/G]TCCTCTACGATCCAA	838447
rs346583843	snp	A/G			intron-variant	?	TAIR10	1:6424945	TCCATCCAAGCTATA[A/G]CAATTGAAACAATTC	838447
rs346601770	snp	C/G			synonymous-codon	?	TAIR10	1:6424795	TGACTTCTTAAAGCT[C/G]CGGGAACTGACGACC	838447
rs346611210	snp	A/T			intron-variant	?	TAIR10	1:6425131	ATTGATAGTTGTGGC[A/T]CTTGTATACTCATGT	838447
rs346617262	snp	G/T			intron-variant	?	TAIR10	1:6423589	TTGAATACTCGTTTA[G/T]TGTAAAATTTGTTTA	838447
rs346638816	snp	C/G			utr-variant-3-prime	?	TAIR10	1:6425592	GATGGCATTGTATTG[C/G]CGGTTAAACTACAGA	838447
rs346645942	snp	A/T			intron-variant	?	TAIR10	1:6423522	GTGAGTTCTTTCAAA[A/T]TTTTTCGGTTATGTA	838447
rs346682932	snp	A/C			missense	?	TAIR10	1:6424674	AGGTTGAATGGGTGA[A/C]AGATATACCACCACA	838447
rs346705766	snp	C/T			synonymous-codon	?	TAIR10	1:6424843	TCGGTCATGGCTAGA[C/T]AGAGCAAAGGAAGCA	838447
rs346725583	snp	A/G			intron-variant	?	TAIR10	1:6424900	CATTAGCTGAGAAAG[A/G]GAATTGAATTACTCA	838447
rs346734077	snp	C/T			intron-variant, missense	?	TAIR10	1:6425463	CAAATCTCATTGTTT[C/T]ACCAGTCCCTTTCTT	838447
rs346786647	snp	A/C			intron-variant	?	TAIR10	1:6423803	GTAGTACTGTTTGCG[A/C]TCAGTACATTAATTA	838447
rs346841353	snp	C/G			intron-variant	?	TAIR10	1:6423678	TTATAAAGACACGGA[C/G]ACTCAATTTAGGAAG	838447
rs346951188	snp	G/T			utr-variant-3-prime	?	TAIR10	1:6425772	TACCATATTCTTCAT[G/T]ATGCAACTGTAGCAA	838447
rs347021552	snp	A/C			intron-variant	?	TAIR10	1:6423794	TCCACAGCAGTAGTA[A/C]TGTTTGCGCTCAGTA	838447
rs347248640	snp	A/C			intron-variant	?	TAIR10	1:6422486	ACTAGCAGTTGCAAA[A/C]TTCATCGACTCATAT	838447
rs347322429	snp	C/T			intron-variant	?	TAIR10	1:6422631	TATGTGCTGAGTTAT[C/T]CTTCTGTCTCTAGAT	838447
rs347352016	snp	A/T			synonymous-codon	?	TAIR10	1:6422100	ATTTTTTTCCCAGGC[A/T]ATTAGCAGTTATTCA	838447
rs347369613	snp	C/G			synonymous-codon	?	TAIR10	1:6422964	TGGAATGGCTGAGCG[C/G]TCTGATGATTTTGAT	838447
rs347399785	snp	G/T			synonymous-codon	?	TAIR10	1:6421438	AATCACTCTCATGTC[G/T]AACGAAGACTCTCTT	838447
rs347451388	snp	A/T			intron-variant	?	TAIR10	1:6424875	CTAGACAAGGAGGTA[A/T]GCAACTATTCATTAG	838447
rs347470493	snp	A/G			synonymous-codon	?	TAIR10	1:6421501	CGAAAATTACGGTCT[A/G]GTGAGTTCTCTTTGG	838447
rs347479737	snp	C/T			intron-variant	?	TAIR10	1:6422208	AAAACCGATGCCATC[C/T]TTTTTACTTCCAATG	838447

Full records

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