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
rs193317844	snp	A/G	0.0590585	0.161373	intron-variant	?	WS195	I:403333	GATTCCAGGAAATTC[A/G]ATTTTCGTAAATTTC	171633
rs193317845	snp	A/G	0.019998	0.0979748	intron-variant	?	WS195	I:407288	TTCATATAATTTTCT[A/G]AAACAACATATTCTG	171633
rs193569502	snp	A/T			missense	?	WS195	I:399960	TTTTTTTGCAGAAGA[A/T]ATCGATTTGGATCGA	171633
rs193569503	snp	A/T			intron-variant	?	WS195	I:400156	ATTGAATAAAAAAAA[A/T]GATTTTTTTAATCGA	171633
rs193569504	snp	C/G			intron-variant	?	WS195	I:400524	GATTCGCGACAATTG[C/G]AGTGAGTCAATGGGA	171633
rs193569505	snp	A/G			intron-variant	?	WS195	I:400526	TTCGCGACAATTGCA[A/G]TGAGTCAATGGGAGG	171633
rs193569506	snp	A/G			intron-variant	?	WS195	I:403136	AACGGTCTCGCATTG[A/G]CCCTCTCGGAAAATG	171633
rs193569507	snp	A/C			intron-variant	?	WS195	I:403168	ATGCTTGAGTAAAAA[A/C]TCACGGAGTTGAAAT	171633
rs193569508	snp	C/T			synonymous-codon	?	WS195	I:403538	GGTCTCGCATTGACC[C/T]TGTCGGAAAATGAAT	171633
rs193569509	snp	A/G			intron-variant	?	WS195	I:404082	TTGTCATTTTTACGG[A/G]ACATTGACACCCTTG	171633
rs193569510	snp	A/T			intron-variant	?	WS195	I:405124	TTCAAAAATTCTTTT[A/T]AAAAAAACTCAATAA	171633
rs193569511	snp	C/T			intron-variant	?	WS195	I:405298	ACACGCCAATGGGGT[C/T]ATAATGACCGAATAT	171633
rs193569512	snp	A/G			intron-variant	?	WS195	I:406646	AAGTTTTTTTTTGCA[A/G]TTTCACTAAATGAGC	171633
rs193569513	snp	C/G			intron-variant	?	WS195	I:406916	GTGGCCTTTGATTGG[C/G]CGTTTAATCGTTGTT	171633
rs193569514	snp	A/T			intron-variant	?	WS195	I:408389	GAAAATCCCGGATTT[A/T]AAAAAAAATAAAATT	171633
rs193569515	snp	A/T			intron-variant	?	WS195	I:408390	AAAATCCCGGATTTA[A/T]AAAAAAATAAAATTT	171633
rs193569517	snp	A/G			missense	?	WS195	I:408666	TTAAGTGCACATTCT[A/G]GTGATGAACAACCAT	171633
rs193569518	snp	G/T			intron-variant	?	WS195	I:408867	AATTAAAAAAAAATT[G/T]TTTAAAGTAATCAAT	171633
rs193569520	snp	A/G			intron-variant	?	WS195	I:409760	AAGTTTGGTACTGCA[A/G]TATTTAAAAAAAAAG	171633
rs193569521	snp	C/G			intron-variant	?	WS195	I:409843	AAAAAAATGTTTTTG[C/G]AAAATTTGAAATTTA	171633
rs193569522	snp	A/T			intron-variant	?	WS195	I:410909	ATTTAGAACTAATTA[A/T]TTTTTAATTTTTTGG	171633
rs193569523	snp	A/G			intron-variant	?	WS195	I:412036	GAAATCTAGATGTCA[A/G]TTTCTTCACAAAATT	171633
rs193569524	snp	A/G			intron-variant	?	WS195	I:412112	TTTAAATCAAAATTT[A/G]GCGATTTTCAAAATG	171633
rs353095821	in-del	-/T			intron-variant	?	WS195	I:407577	AAAGGATTTTTTCAA[-/T]TTTTTTTTTCTAAAA	171633
rs353096269	snp	C/T			intron-variant	?	WS195	I:402929	CACGGAGTTGAAATC[C/T]GCGGAATTCGATTTT	171633
rs353096800	snp	A/T			intron-variant	?	WS195	I:403502	TCAATTAAAATTTTT[A/T]TAAAAAATTTTCAGA	171633
rs353103215	snp	A/T			intron-variant	?	WS195	I:407000	AAAGACCATAAATGT[A/T]TTTAAATCAACGATT	171633
rs353105738	snp	C/T			intron-variant	?	WS195	I:408117	AAGCTGATTTTTCGC[C/T]AAAGTTCAAAAAAAT	171633
rs353108632	snp	G/T			intron-variant	?	WS195	I:399700	AAAATCGGGTGTTTA[G/T]GCTCCGCCCACAAAA	171633
rs353109263	snp	G/T			intron-variant	?	WS195	I:405888	AAAAATTCAAAAAAT[G/T]TTTCTACATTTTATA	171633
rs353115385	in-del	-/A			intron-variant	?	WS195	I:408493	TCATATTCTTTGAAT[-/A]AAAAAAAATCTGAAT	171633
rs353123892	snp	G/T			intron-variant	?	WS195	I:402476	TTCGGTGAAAAATGA[G/T]CAAAAATGAGCTGAA	171633
rs353125491	in-del	-/A			intron-variant	?	WS195	I:399076	TAAGCTGAAAAGTGG[-/A]AAAAAAAATGCATTT	171633
rs353127669	snp	G/T			intron-variant	?	WS195	I:410278	CAATTTTGAGTCTAA[G/T]AAGCCAATAAAAAAT	171633
rs353128727	in-del	-/T			intron-variant	?	WS195	I:407794	AAAGAAAAAAAATCG[-/T]TTTTTTTTTTCGAAT	171633
rs353133983	snp	A/G			intron-variant	?	WS195	I:408284	CTTTAGCTTTCGGCC[A/G]AAATTTTATCATAAA	171633
rs353134663	snp	C/T			intron-variant	?	WS195	I:402210	AAAATTGTTTTTTTA[C/T]TAAATTTTTTTTGGA	171633
rs353137938	snp	A/T			intron-variant	?	WS195	I:403503	CAATTAAAATTTTTT[A/T]AAAAAATTTTCAGAG	171633
rs353139053	snp	A/G			intron-variant	?	WS195	I:405908	ATGACCGAATATCAT[A/G]ATAAAAAAATTCAAA	171633
rs353140623	in-del	-/T			intron-variant	?	WS195	I:406052	AATATTTTAAATTAA[-/T]TTTTTTTTTGCAGAT	171633
rs353141091	snp	A/C			intron-variant	?	WS195	I:408994	AAAAATTCAAACTAC[A/C]ATACTACGATAACAA	171633
rs353145813	snp	A/G			intron-variant	?	WS195	I:405817	ACAAATCCAATTGGC[A/G]GAAATTCAAAAATAA	171633
rs353147734	snp	C/T			intron-variant	?	WS195	I:399858	CGTCAAATCTGGTGC[C/T]TTGGCTCCGCCCACA	171633
rs353150611	in-del	-/T			intron-variant	?	WS195	I:399396	AACTGAAAAAAAAAA[-/T]CAATTTATCTGAAAT	171633
rs353150956	in-del	-/T			intron-variant	?	WS195	I:401945	AAACTTTAAAAGTTC[-/T]TTTTTTTTCCAGGAC	171633
rs353152088	snp	A/T			intron-variant	?	WS195	I:407947	GAAAAAATTAAAAAA[A/T]TTTTTTGCGTATTTG	171633
rs353153332	snp	A/G			intron-variant	?	WS195	I:408312	AAAAATTTCCGGAAT[A/G]CATAGTTTTAGAGAA	171633
rs353153493	snp	A/G			intron-variant	?	WS195	I:402553	AAACAATTTTCGTGG[A/G]TTTCAACTTCGCGAA	171633
rs353159912	snp	A/G			intron-variant	?	WS195	I:406992	TGTACCCCAAAGACC[A/G]TAAATGTATTTAAAT	171633
rs353165973	snp	A/G			intron-variant	?	WS195	I:399695	CGCGTAAAATCGGGT[A/G]TTTATGCTCCGCCCA	171633
rs353168115	in-del	-/A			intron-variant	?	WS195	I:409766	GGTACTGCAGTATTT[-/A]AAAAAAAAGTTTTTC	171633
rs353174742	snp	A/G			intron-variant	?	WS195	I:410109	ACTCGAAATTTGACG[A/G]TGATTTCAAAAAAAA	171633
rs353175494	snp	A/T			intron-variant	?	WS195	I:405905	TTTTTTGAATTTTTT[A/T]ATCATAATATTCGGT	171633
rs353177710	in-del	-/T			intron-variant	?	WS195	I:400852	AACAATTTTTTGAAA[-/T]TTTTTTTATAGCATT	171633
rs353181693	snp	A/G			intron-variant	?	WS195	I:409312	TATTTTGCGCGTCAA[A/G]TATGTTGCGTAGTAC	171633

Full records

It may take some time, please wait.