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
rs193925288	snp	C/T			intron-variant	?	TAIR10	1:9557172	TGAGAGCAGGTTATG[C/T]TGAGGATTTAAATCT	839642
rs346442634	snp	C/T			utr-variant-3-prime	?	TAIR10	1:9554941	CAAAACGACGGTGTA[C/T]TGGTCACTCAGGCAG	839642
rs346475340	snp	A/G			intron-variant	?	TAIR10	1:9555049	ATGGTCCCATTCCCT[A/G]TTCAGAAAACCTCAT	839642
rs346499758	snp	A/G			synonymous-codon	?	TAIR10	1:9555143	TCCATTGAGTTTTAA[A/G]AGCTTGCCCTCGACC	839642
rs346591335	snp	A/C			missense	?	TAIR10	1:9555716	ACTTCCTTCTGCATC[A/C]TCCCACCGACCATAC	839642
rs346662570	snp	C/G			missense	?	TAIR10	1:9558127	GCTTTAGGGTTACAG[C/G]TTGATATAGAAGAAG	839642
rs346732762	snp	A/G			synonymous-codon	?	TAIR10	1:9558060	ATCCTCACTCGAACT[A/G]GTATCAGCTCCATCA	839642
rs346820016	snp	A/C			intron-variant	?	TAIR10	1:9555086	AAACCGAAAAGACGA[A/C]GAAATGATGGTCGGC	839642
rs346857375	snp	C/G			intron-variant	?	TAIR10	1:9555543	AATGTCACCTACCAA[C/G]AATTTGTGACCCTAT	839642
rs346903093	snp	C/T			intron-variant	?	TAIR10	1:9557352	AAAACAATCATCGTC[C/T]AGATAAAAGCATAGA	839642
rs346909139	snp	C/G			synonymous-codon	?	TAIR10	1:9556544	AGTGCCTTCTCCAAC[C/G]AGCTCTTCAGTAGCG	839642
rs346983530	snp	A/C			missense	?	TAIR10	1:9558123	TGGGGCTTTAGGGTT[A/C]CAGGTTGATATAGAA	839642
rs346985962	snp	A/G			intron-variant	?	TAIR10	1:9555090	CGAAAAGACGAAGAA[A/G]TGATGGTCGGCTCTT	839642
rs347073260	snp	G/T			missense	?	TAIR10	1:9556554	CCAACCAGCTCTTCA[G/T]TAGCGTCATCACTGC	839642
rs347125831	snp	C/G			missense	?	TAIR10	1:9556717	CTTCTTTTTTATCCA[C/G]CTTCAGTTCACTTCC	839642
rs347149087	snp	C/G			intron-variant	?	TAIR10	1:9555549	ACCTACCAACAATTT[C/G]TGACCCTATCTTAGA	839642
rs347155220	snp	A/T			utr-variant-3-prime	?	TAIR10	1:9554810	TCTACAACCAAAATA[A/T]CTAAAAAAAGAAAAC	839642
rs347175047	snp	C/T			missense	?	TAIR10	1:9557060	CGTCAGTGTCTTTAA[C/T]AACGAAAATCTCAAA	839642
rs347222022	snp	C/T			missense	?	TAIR10	1:9558274	ATTTGGCCGATAAGA[C/T]ATGGTTGAGTTGTCG	839642
rs347253908	snp	C/T			intron-variant	?	TAIR10	1:9555272	CAAATGTCAATGTGG[C/T]TGGAACCCATGAAAT	839642
rs347291861	snp	A/C			missense	?	TAIR10	1:9555142	TTCCATTGAGTTTTA[A/C]GAGCTTGCCCTCGAC	839642
rs347306770	snp	C/T			missense	?	TAIR10	1:9557764	GTAACTGGCGCATGA[C/T]CTCAGCGACAGCATC	839642
rs347333842	snp	A/C			intron-variant	?	TAIR10	1:9557458	TATGTCAGGAAACAT[A/C]TATTACTTCAACTAA	839642
rs347340977	snp	C/T			missense	?	TAIR10	1:9556759	AAATGGATGGGTCAT[C/T]GATCGAGGATTTCGA	839642
rs347398520	snp	A/G			synonymous-codon	?	TAIR10	1:9555976	TCCTTTTTGTGCCTG[A/G]TTTATAGCAAGCTTG	839642
rs347402178	snp	C/G			intron-variant	?	TAIR10	1:9555294	CCATGAAATGTCTAA[C/G]CAATTGTTTCAATAG	839642
rs347407318	snp	A/T			synonymous-codon	?	TAIR10	1:9558210	CGAGAGCTCCGGCTT[A/T]AGAGAATTTCTGGGG	839642

Full records

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