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
rs193334847	snp	C/G	0.0301437	0.119009	missense	such-1	WS195	III:11517595	CTGGACACGACGCTC[C/G]TTTTCCACCGATTCC	176583
rs193334848	snp	C/G	0.0200984	0.0982103	intron-variant	such-1	WS195	III:11517659	TTTGCAAAAATTCGC[C/G]GCATCGCACAGAAAA	176583
rs193359761	snp	C/T			intron-variant	such-1	WS195	III:11516785	TTTTTAATGCTTTAT[C/T]TCAGTTTTTTTAAAA	176583
rs193601233	snp	C/T			synonymous-codon	such-1	WS195	III:11515798	GATATTCTCGGGGAA[C/T]CGGTTTTTAAGAATA	176583
rs193601234	snp	A/T			intron-variant	such-1	WS195	III:11516562	TAATCGATTTTTTTT[A/T]AAAGTTTTACCGGGG	176583
rs193601235	snp	C/T			intron-variant	such-1	WS195	III:11519156	GGGGTAGATTTGCAG[C/T]AAAATCTCCAAAATA	176583
rs193601236	snp	A/G			intron-variant	such-1	WS195	III:11519823	ATTGATTAATGTATG[A/G]TTTCCGTAAATCGAC	176583
rs193601237	snp	A/G			intron-variant	such-1	WS195	III:11520024	CTTATTTTAGAGAGA[A/G]CTTAGACAAAATTTA	176583
rs193601239	snp	A/G			intron-variant	such-1	WS195	III:11520275	AGCTTAAACTGAGAA[A/G]TTTCCCTTTTTCAGT	176583
rs193601240	snp	C/G			synonymous-codon	such-1	WS195	III:11521279	TGACATTGCTTTTGT[C/G]GGGCATAGTTGGACG	176583
rs193601241	snp	C/T			intron-variant	such-1	WS195	III:11522248	AAATCGAATTTTCAC[C/T]GATTTCCTACAGAAA	176583
rs353099571	snp	A/T			intron-variant	such-1	WS195	III:11519131	TTGCAGTGTTTTTTT[A/T]AATGTTAATGGGGTA	176583
rs353099686	snp	A/C			intron-variant	such-1	WS195	III:11518761	GTTGAATTTTGAAAA[A/C]CTCAAAACTTTTTCA	176583
rs353103092	snp	A/T			intron-variant	such-1	WS195	III:11516479	CGCACACTTTTTAAA[A/T]TAAAAACAAAAATTT	176583
rs353118046	in-del	-/T			intron-variant	such-1	WS195	III:11522633	ACCCAAACAAAAATC[-/T]TTTTTTTTTTGTCAA	176583
rs353121673	in-del	-/A			intron-variant	such-1	WS195	III:11514012	TTAAAGTTGAGCAAG[-/A]AATTAGAACATAATA	176583
rs353125976	snp	A/G			intron-variant	such-1	WS195	III:11513822	ACAATATATTACGGG[A/G]ACACAAAATTTCGAG	176583
rs353128103	in-del	-/A			intron-variant	such-1	WS195	III:11521952	TTTGACTGATAACCC[-/A]AAAAAAAAATCAGTG	176583
rs353139181	snp	A/G			intron-variant	such-1	WS195	III:11521865	GACGAAAAAAAATTT[A/G]AACCCATTCGAAAGA	176583
rs353142219	in-del	-/T			intron-variant	such-1	WS195	III:11519214	AGAGCTGCAGTACCA[-/T]TTTTTTCAACTGAAA	176583
rs353152649	snp	C/G			missense	such-1	WS195	III:11517412	CACAGTAAAAACTTG[C/G]ACATTGACACCAAAA	176583
rs353154969	snp	A/T			intron-variant	such-1	WS195	III:11516244	TTCTCCGTTTTTTTT[A/T]AATCGAAGTTCCAGC	176583
rs353157066	in-del	-/T			intron-variant	such-1	WS195	III:11522310	CAAACCGAAAAAACA[-/T]TTTTTTTCTTCAATT	176583
rs353158131	snp	A/G			intron-variant	such-1	WS195	III:11518749	TCACCGAAAAAAGTT[A/G]AATTTTGAAAACCTC	176583
rs353162675	snp	A/C			intron-variant	such-1	WS195	III:11520645	CTGTGAGTTTTTTAA[A/C]GGAAAATTTTCAATT	176583
rs353165070	snp	A/T			intron-variant	such-1	WS195	III:11521969	AAAAAAAATCAGTGT[A/T]ACCGGTTTTTAGACT	176583
rs353167323	in-del	-/CA			intron-variant	such-1	WS195	III:11514528	AAAATATGAACTGCG[-/CA]TTGAACGAAACAAAG	176583
rs353167503	snp	A/G			intron-variant	such-1	WS195	III:11520300	TTCAGTTAAAAAAAT[A/G]GTACTGCAGCTCTCA	176583
rs353171116	snp	A/C			intron-variant	such-1	WS195	III:11519334	ATTTTCGTATTCAAT[A/C]AAAATGGGGGAAATT	176583
rs353174477	in-del	-/A			intron-variant	such-1	WS195	III:11520803	CTTTTTTTTCAGTTG[-/A]AAAAAATGGTACTGC	176583
rs353174612	in-del	-/A			intron-variant	such-1	WS195	III:11513493	TGCTTTTTTTTAAGT[-/A]AAAAAAAAAAACAAA	176583
rs353181471	snp	A/G			synonymous-codon	such-1	WS195	III:11512877	CGCCTCAATCTTTCC[A/G]AATCGTTCCTTCGCC	176583
rs353182254	in-del	-/T			intron-variant	such-1	WS195	III:11517719	GGCACGGTTTTCCAC[-/T]TTTTTTTTTCGAATA	176583

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