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

CHR8

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs346457472	snp	C/T			missense	CHR8	TAIR10	2:8132698	AAACAGATGTGGAAA[C/T]GACTGATAAAACTGG	816391
rs346496103	snp	A/G			missense	CHR8	TAIR10	2:8131381	CAGACCGTCCATCGA[A/G]TTATTATGACTGGGG	816391
rs346574566	snp	C/T			intron-variant	CHR8	TAIR10	2:8130462	GATTGCTGTTTGGGC[C/T]CTTTGATTGAATTTC	816391
rs346619287	snp	A/G			intron-variant	CHR8	TAIR10	2:8131626	CTCTAAAGAATTCTT[A/G]ACAATGTGCAGGTGT	816391
rs346674806	snp	C/T			intron-variant	CHR8	TAIR10	2:8130537	GATATTGGATCTTCC[C/T]GATGTTGAGATATCA	816391
rs346872663	snp	C/G			synonymous-codon	CHR8	TAIR10	2:8131089	AGCACAAGATTCTGG[C/G]CACGGCAAAGGTCAA	816391
rs346922329	snp	A/G			synonymous-codon	CHR8	TAIR10	2:8130825	ATGCATCTTTCGTAA[A/G]CTTTTTGACTACCAA	816391
rs346924307	snp	A/G			synonymous-codon	CHR8	TAIR10	2:8131488	TGTGTTTGAGGCAGA[A/G]TTTTCTGTTCCCATA	816391
rs346931654	snp	C/T			missense	CHR8	TAIR10	2:8129860	TTGATGGAGCTTCAG[C/T]TGGTTTTGTTGAAAC	816391
rs346961250	snp	G/T			missense	CHR8	TAIR10	2:8131047	GAAATGGTACCCAGA[G/T]TTTCACGTGGAAATA	816391
rs346965268	snp	G/T			synonymous-codon	CHR8	TAIR10	2:8132166	TCTGACGACGAAGGT[G/T]GGTGGTTTGGGAACA	816391
rs347006837	snp	C/T			synonymous-codon	CHR8	TAIR10	2:8129178	GACGAGGATCAGTTT[C/T]TGTTGAGTAGCTTAG	816391
rs347056931	snp	A/G			synonymous-codon	CHR8	TAIR10	2:8131200	GTGGGATTCTTTGTT[A/G]AACCGGGTTCTAAAT	816391
rs347128946	snp	C/T			synonymous-codon	CHR8	TAIR10	2:8132905	CATAATGAATGCAAA[C/T]GACGAGGAAGAGAAG	816391
rs347185084	snp	A/C			intron-variant	CHR8	TAIR10	2:8132829	GACTTACTTTCCCAT[A/C]ATTTCCAATTCCCTT	816391
rs347217404	snp	C/T			synonymous-codon	CHR8	TAIR10	2:8133400	GGACATAGTTTCTTT[C/T]AATGACAAGCAGTTG	816391
rs347318472	snp	C/G			missense	CHR8	TAIR10	2:8130188	CGCTGGCTGCAAAGG[C/G]TCGTCCCACAACCAA	816391
rs347348162	snp	C/T			synonymous-codon	CHR8	TAIR10	2:8132603	GGAAGAGATAAACAT[C/T]GTAGGAGTTCAATCA	816391
rs347357451	snp	C/T			intron-variant	CHR8	TAIR10	2:8132295	GTGCAAAAAACCCGT[C/T]GTGGCCATAAATAAC	816391
rs347462419	snp	A/T			intron-variant	CHR8	TAIR10	2:8129890	CGGTACGTCCAGTTA[A/T]CTTCTAAAGGTTTTA	816391
rs347475036	snp	A/G			missense	CHR8	TAIR10	2:8133332	AAGATATGCAGCTTT[A/G]TACAGCAAAAAGGTG	816391