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
rs193326751	snp	A/G	0.0771698	0.180637	missense	?	WS195	II:8082132	CATTTTTCGATAAAT[A/G]GAATTCCATGTCAAT	174300
rs193326752	snp	C/T	0.4488	0.151587	synonymous-codon	?	WS195	II:8082340	CATCGCACAATACGT[C/T]ACTTCGATTTGTTCA	174300
rs193326753	snp	A/G	0.0215028	0.101435	intron-variant	?	WS195	II:8082451	AGTTTTCCTTTTTAA[A/G]TATAGATTTTTTTGT	174300
rs193587769	snp	C/T			synonymous-codon	?	WS195	II:8083767	CGTATACTTTCGAGG[C/T]GCAATCTTTGTAATC	174300
rs353097144	snp	G/T			intron-variant	?	WS195	II:8082466	ATATAGATTTTTTTG[G/T]TTTTTTTTTCATTTT	174300
rs353115842	snp	G/T			intron-variant	?	WS195	II:8081989	AACTATTAGGAAATG[G/T]AGATTACTCAGAAAA	174300
rs353118099	snp	A/G			intron-variant	?	WS195	II:8083289	GATGAATGAGAAAAG[A/G]CGTGCGCCTTTAAAG	174300
rs353120350	snp	A/G			synonymous-codon	?	WS195	II:8086114	CGGTTGTTCGTGCCA[A/G]CTTAATGGAGCACAG	174300
rs353120868	in-del	-/T			intron-variant	?	WS195	II:8082457	CTTTTTAAATATAGA[-/T]TTTTTTTGTTTTTTT	174300
rs353145727	snp	A/T			intron-variant	?	WS195	II:8083029	ATACAAAATAAAATT[A/T]AAAAAAAACTTTTTT	174300
rs353150137	snp	A/C			missense	?	WS195	II:8086978	GAAAACGGCGCCAAG[A/C]CTGAAATGTACAAAA	174300
rs353160237	snp	G/T			intron-variant	?	WS195	II:8082465	AATATAGATTTTTTT[G/T]TTTTTTTTTTCATTT	174300
rs353162535	snp	A/G			missense	?	WS195	II:8081833	CGTTCTAGGTCCATC[A/G]CGGTGTTCACAACCA	174300
rs353175796	snp	A/T			intron-variant	?	WS195	II:8083030	TACAAAATAAAATTA[A/T]AAAAAAACTTTTTTA	174300
rs353178013	snp	A/C			intron-variant	?	WS195	II:8084409	TTCATCAAAACTTCA[A/C]ACATAAGGCAGAAAT	174300

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