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

ULP2B

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs2228896	snp	C/T	0.5	0	missense	?	TAIR10	1:3153503	GGTTATCGTGATCTA[C/T]ATCTGTTTCCTTTGC	837501
rs346565673	snp	C/T			intron-variant	?	TAIR10	1:3150762	AGAGAACTGCCACAG[C/T]TTTTCGTACTTGTAG	837501
rs346591866	snp	C/T			synonymous-codon	?	TAIR10	1:3148670	TACCTCTCTTGCCGA[C/T]GAGTCGTTACTAAGA	837501
rs346635561	snp	A/G			intron-variant	?	TAIR10	1:3149092	AAAGCTGAGAAAATC[A/G]GAGAAAAAGCATTAT	837501
rs346646333	snp	A/T			intron-variant	?	TAIR10	1:3149707	ATTTATCCATCAATG[A/T]CAGAGGTTACCAAGT	837501
rs346650380	snp	G/T			intron-variant	?	TAIR10	1:3152599	AAATTGACCAGCAAA[G/T]ATTGTCAGAGTGATA	837501
rs346658291	snp	A/G			missense	?	TAIR10	1:3148498	GGAGAGGTAGTTTCC[A/G]TGATGCATTGAAAGT	837501
rs346679706	snp	C/T			missense, intron-variant	?	TAIR10	1:3153080	ATTGAAATCAAGACA[C/T]GGTCAGACATAGGAG	837501
rs346698722	snp	C/T			missense	?	TAIR10	1:3148660	GAACTTTTAGTACCT[C/T]TCTTGCCGACGAGTC	837501
rs346730637	snp	A/G			intron-variant	?	TAIR10	1:3150084	TCATTATCTGCCCTG[A/G]AAATAGTAAAAAGAT	837501
rs346753482	snp	A/G			intron-variant	?	TAIR10	1:3151111	AAATAGTTCACAGCA[A/G]CACATGCCAGAGTAT	837501
rs346785730	snp	A/G			synonymous-codon	?	TAIR10	1:3148263	CTCAGTGGTATGGTC[A/G]GCAGTGTTAGAACCC	837501
rs346815904	snp	C/T			synonymous-codon	?	TAIR10	1:3152014	CGCAATCTTTAACTC[C/T]TCCATGTCTGGAAAC	837501
rs346828904	snp	C/G			intron-variant	?	TAIR10	1:3150365	AATATCAGCTCGTTG[C/G]CAAGTGAGAAACGTA	837501
rs346920489	snp	C/T			intron-variant	?	TAIR10	1:3151389	TGGTACATGTACTCC[C/T]GAAGTAAAACAGAAG	837501
rs347036891	snp	A/G			intron-variant	?	TAIR10	1:3149175	TTCAACTTCTTTCAA[A/G]CGGACTCATGAAATC	837501
rs347186770	snp	C/T			missense	?	TAIR10	1:3152861	ATTATAACAGCGGTG[C/T]TTAAGTCAATCTGCG	837501
rs347204955	snp	A/G			missense	?	TAIR10	1:3152527	TATACATACCTTCAT[A/G]GCAATTTTCATCCTT	837501
rs347306318	snp	C/T			missense	?	TAIR10	1:3152868	CAGCGGTGCTTAAGT[C/T]AATCTGCGAAGTGGA	837501
rs347390265	snp	A/C			missense	?	TAIR10	1:3152856	AAGTCATTATAACAG[A/C]GGTGCTTAAGTCAAT	837501
rs347465487	snp	A/C			intron-variant	?	TAIR10	1:3153971	AAACAGAAGAATTCC[A/C]AGGTTAGCTTAACTT	837501