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
rs193318717	snp	G/T	0.316345	0.241036	intron-variant	?	WS195	I:2502498	ATCAATAATTTTTTT[G/T]GAAAATTGCCAAGAA	171811
rs193318718	snp	A/C	0.0492297	0.148967	intron-variant	?	WS195	I:2502502	ATAATTTTTTTTGAA[A/C]ATTGCCAAGAAAAAT	171811
rs193318719	snp	C/T	0.0210502	0.100409	intron-variant	?	WS195	I:2502601	AAAAAACTATATTTT[C/T]CGATTAAAAAATCGA	171811
rs193318720	snp	C/T	0.207612	0.24638	intron-variant	?	WS195	I:2504855	AAATTGTAAATTCAT[C/T]TAGAAATTGATCTTT	171811
rs193318721	snp	A/T	0.0205106	0.0991697	intron-variant	?	WS195	I:2504959	CAATTTTTGTACTAA[A/T]AATTGCCAAAAAATT	171811
rs193571816	snp	G/T			synonymous-codon	?	WS195	I:2500103	TTTCTCTCCACGTGG[G/T]GATACTGTCTTCTCA	171811
rs193571817	snp	A/C			intron-variant	?	WS195	I:2500427	AGTAGTTGGAAGCTG[A/C]AAAAGTGCAAAAATT	171811
rs193571818	snp	A/G			intron-variant	?	WS195	I:2501404	AATTTGCCGGAATGG[A/G]AAATTTCTGGCAAGT	171811
rs193571819	snp	C/G			intron-variant	?	WS195	I:2501424	TTCTGGCAAGTTCGG[C/G]AACTTGCCGGTATTG	171811
rs193571820	snp	A/G			intron-variant	?	WS195	I:2502691	TCGAGAAAAAAATCG[A/G]TACTTTTTGAAAAAA	171811
rs193571821	snp	G/T			intron-variant	?	WS195	I:2502854	TTTTCCAGTGGGAAA[G/T]CTCTATTTTTAGTAA	171811
rs193571822	snp	C/T			intron-variant	?	WS195	I:2503434	AATTTCACTAAAAAT[C/T]GATAGTTTTTTGGCT	171811
rs193571823	snp	A/G			intron-variant	?	WS195	I:2503488	ATGATTCAAATCCAA[A/G]AAATTGTAATTTTTT	171811
rs193571824	snp	C/T			intron-variant	?	WS195	I:2503919	TGAAAAAAAATCAAT[C/T]TTTGGGAAAAAAAAA	171811
rs193571825	snp	A/G			synonymous-codon	?	WS195	I:2504022	GCCAAAATTTCCAGG[A/G]AAATTCCGTTCGGCA	171811
rs193571826	snp	G/T			intron-variant	?	WS195	I:2504540	TTTTTTTTCAAAAAT[G/T]CTTGGGAAAAAATGT	171811
rs193571827	snp	A/T			intron-variant	?	WS195	I:2504719	GTGATAAATTGATAT[A/T]TTCCAAAAAATCGGA	171811
rs353103150	in-del	-/A/AA			intron-variant	?	WS195	I:2504460	GAAATTGAATTTTTC[-/A/AA]AAAAAAAAAAATTAA	171811
rs353103862	snp	A/T			intron-variant	?	WS195	I:2504679	GAAATTTATGAAAAA[A/T]GTCACAATTTCTTGG	171811
rs353106574	snp	C/T			intron-variant	?	WS195	I:2501178	AATTTCCGGCAAATT[C/T]GACGAATCGGCAACT	171811
rs353108655	snp	A/C			intron-variant	?	WS195	I:2502857	TCCAGTGGGAAAGCT[A/C]TATTTTTAGTAATTA	171811
rs353114047	snp	A/T			intron-variant	?	WS195	I:2500509	AAAATTTTTTTTTGA[A/T]GATTTTCCTTCAAAA	171811
rs353114049	snp	A/T			intron-variant	?	WS195	I:2504816	AAATGGATTTTTCAT[A/T]AAAAAAAACCAAATT	171811
rs353115264	snp	C/T			intron-variant	?	WS195	I:2500600	CAATTTGGCAATTTG[C/T]CGGGATTGAAAATTT	171811
rs353118467	snp	A/C			utr-variant-3-prime	?	WS195	I:2505783	TTATCGGGTTTTCTA[A/C]GAAAAATGTATTAAA	171811
rs353119837	snp	A/G			intron-variant	?	WS195	I:2501281	AATTTAAAAATTTCC[A/G]GCAAAAAAAAATTGA	171811
rs353120738	snp	C/T			intron-variant	?	WS195	I:2503935	TTTGGGAAAAAAAAA[C/T]ATTTTTCGTTTCCTG	171811
rs353122060	snp	C/T			intron-variant	?	WS195	I:2501857	ATTGAAAATTTCTGG[C/T]AAAAAAAAATTGAAA	171811
rs353128315	snp	A/G			intron-variant	?	WS195	I:2504156	TGTAAGATTTTGCAC[A/G]AAAATAGGATATTTT	171811
rs353130669	snp	A/G			synonymous-codon	?	WS195	I:2505590	TAATGATGTATTCGG[A/G]GAGCCGACGATTCGA	171811
rs353131002	in-del	-/G			intron-variant	?	WS195	I:2500424	TGAGTAGTTGGAAGC[-/G]TGAAAAAGTGCAAAA	171811
rs353135066	in-del	-/A			intron-variant	?	WS195	I:2502583	ATTTCTCTAAATTAG[-/A]AAAAAAAACTATATT	171811
rs353144015	snp	G/T			intron-variant	?	WS195	I:2503037	TTTCACGTATTTTCA[G/T]CTTTAAAAATATTTT	171811
rs353145147	snp	A/G			intron-variant	?	WS195	I:2500764	GTTCGACAACTTGCC[A/G]GAATTAGAAATTTCC	171811
rs353161933	in-del	-/A			intron-variant	?	WS195	I:2504905	ATCTTTCGGCAGATC[-/A]AAAAAAAAATTAGAA	171811
rs353165110	snp	C/G			missense	?	WS195	I:2502191	GTATCACGTGATGAT[C/G]AAACAATGGCAATTG	171811
rs353166115	snp	G/T			stop-gained	?	WS195	I:2505660	GCTGAGGAGGAATAT[G/T]AAGAAAATATGCAGA	171811
rs353167080	snp	C/T			intron-variant	?	WS195	I:2503517	TTCAAATTTTAAGGC[C/T]TATTAAACTACATTT	171811
rs353175225	snp	A/T			intron-variant	?	WS195	I:2500867	CGGCAAAAAAATTAT[A/T]AAAAAATCCGGTAGT	171811
rs353175884	snp	A/G			missense	?	WS195	I:2505550	AAATGAATGTGAAAA[A/G]TTCCTCCACGGCTCT	171811
rs353177515	snp	C/T			intron-variant	?	WS195	I:2501280	AAATTTAAAAATTTC[C/T]AGCAAAAAAAAATTG	171811

Full records

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