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
rs105014835	snp	A/G	0	0	intron-variant	Klhl38	Rn_Celera	7:98190295	CATGTACATTCCAGG[A/G]TTTGAGCTGAGGTCA	314996
rs105197536	snp	A/C	0	0	intron-variant	Klhl38	Rn_Celera	7:98190309	GGTTTGAGCTGAGGT[A/C]ATCAGTCTTGTGACA	314996
rs105287438	snp	C/T	0	0	upstream-variant-2KB	Klhl38	Rn_Celera	7:98197188	GGTGAGTGTTTACGT[C/T]GGTATAAATAGAACC	314996
rs105328764	snp	G/T	0.5	0	intron-variant	Klhl38	Rn_Celera	7:98191026	AAACTTCTTTGCATA[G/T]AAAATATAATTTCTA	314996
rs105368874	snp	C/T	0.5	0	intron-variant	Klhl38	Rn_Celera	7:98191115	GCACTTGGTAGAGTG[C/T]ACTATGTATGTATGT	314996
rs106451445	snp	C/T	0	0	utr-variant-5-prime	Klhl38	Rn_Celera	7:98196929	TAAAGCCATAAACCC[C/T]GGGCCTTTCCGTTGG	314996
rs106610509	snp	C/T	0	0	intron-variant	Klhl38	Rn_Celera	7:98190344	TCATTATCATTGACG[C/T]AAGTAGTCATTTAAA	314996
rs106686563	snp	A/G	0	0	intron-variant	Klhl38	Rn_Celera	7:98190500	GATGAGACTAATGGC[A/G]GTATTTCCATTGAAT	314996
rs107446548	snp	C/G	0	0	intron-variant	Klhl38	Rn_Celera	7:98190343	GTCATTATCATTGAC[C/G]TAAGTAGTCATTTAA	314996
rs197120000	snp	A/C	0	0	intron-variant	Klhl38	Rn_Celera	7:98191448	TTCTGGTCCCTAGAG[A/C]CACTGCGTGCATGTG	314996
rs197136369	snp	G/T	0	0	intron-variant, utr-variant-5-prime	Klhl38	Rn_Celera	7:98196246	GGGAAGCCTCAAATG[G/T]AGGCAAAGCCAAGGC	314996
rs197306032	snp	A/G	0	0	downstream-variant-500B	Klhl38	Rn_Celera	7:98187535	CATAGGTGAGAAATA[A/G]CTTTCCTACATACTG	314996
rs197309595	snp	C/T	0	0	intron-variant	Klhl38	Rn_Celera	7:98192916	TGAGCCTCCTCCTTT[C/T]TCTTCTGGGCCTTTG	314996
rs197535705	snp	C/T	0	0	intron-variant	Klhl38	Rn_Celera	7:98191650	GGTTGTTTTTGAGAC[C/T]GAGACCCTGTCGGGA	314996
rs197550769	snp	A/G	0	0	intron-variant, utr-variant-5-prime	Klhl38	Rn_Celera	7:98196248	GAAGCCTCAAATGGA[A/G]GCAAAGCCAAGGCTC	314996
rs197679757	snp	A/G	0	0	intron-variant	Klhl38	Rn_Celera	7:98190058	TTAAAAGAGAAAAGA[A/G]GTAGTTGTTTGTTAC	314996
rs197803248	snp	A/G	0	0	intron-variant	Klhl38	Rn_Celera	7:98193033	TGGGCCCTGTCTTCC[A/G]TGCATCCCAGCATCC	314996
rs197856418	snp	A/G	0	0	synonymous-codon	Klhl38	Rn_Celera	7:98188871	GTTGGACTGAGGATC[A/G]TAAGCAAGAATCCTC	314996
rs197871017	snp	C/T	0	0	intron-variant	Klhl38	Rn_Celera	7:98191551	AGAATTTGACATTCA[C/T]GCTTCATCAGGTAGA	314996
rs197884658	snp	A/G	0	0	intron-variant	Klhl38	Rn_Celera	7:98194745	TAAAGACACACATAT[A/G]TACATGTGTGCATGC	314996
rs197906216	snp	A/G	0	0	downstream-variant-500B	Klhl38	Rn_Celera	7:98187474	CTCCAGCGTGTGGGC[A/G]TTCTGGAACCAGAGC	314996
rs198137369	snp	A/G	0	0	intron-variant	Klhl38	Rn_Celera	7:98189194	CTAATTTACTCCAGA[A/G]CCATAGTCATTCAAG	314996
rs198173179	snp	C/T	0	0	intron-variant, utr-variant-3-prime	Klhl38	Rn_Celera	7:98192515	TGAAAGTGTCTAAGC[C/T]ATCATCATTCCTTGC	314996
rs198227237	snp	C/G	0	0	downstream-variant-500B	Klhl38	Rn_Celera	7:98187612	TGGTGGTCTTCAGTG[C/G]TCACAGCAGAACTGG	314996
rs198353675	snp	G/T	0	0	missense	Klhl38	Rn_Celera	7:98195909	ATCAGGGGGAGGACG[G/T]TGGCAGCTGAGATGT	314996
rs198543840	snp	C/T	0	0	downstream-variant-500B	Klhl38	Rn_Celera	7:98187780	GGTGACCATATCACT[C/T]GGGCAGCACTGAGAA	314996
rs198544599	snp	C/G	0	0	intron-variant	Klhl38	Rn_Celera	7:98191336	CAGTGCTTAAGAGAG[C/G]TGGGTGCTCTTCCTG	314996
rs198633103	snp	A/G	0	0	intron-variant	Klhl38	Rn_Celera	7:98191575	AGGTAGATAGACTCA[A/G]AGGAGCTCAGTGATT	314996
rs198821149	snp	A/T	0	0	intron-variant	Klhl38	Rn_Celera	7:98192993	TCTGACTTCCTCAGC[A/T]GTCAGAGAGCTCTTT	314996
rs198821978	snp	G/T	0	0	intron-variant	Klhl38	Rn_Celera	7:98193734	AAAGGATTTTGCTTA[G/T]TATGTTTCAACAAAA	314996
rs198847580	snp	A/G	0	0	synonymous-codon	Klhl38	Rn_Celera	7:98188718	CGTCTCTGGGTCATA[A/G]CAGTCAAAGGAAGCT	314996
rs198971417	snp	A/G	0	0	utr-variant-3-prime	Klhl38	Rn_Celera	7:98188192	GAGGGGTGATTCCAA[A/G]GGTTCAAGGGTTCTC	314996
rs199028259	snp	G/T	0	0	intron-variant	Klhl38	Rn_Celera	7:98190208	TGTGTGTGTGTGTTT[G/T]TGTGTGTAGATGCCT	314996
rs199261185	snp	A/G	0	0	downstream-variant-500B	Klhl38	Rn_Celera	7:98187523	TCCAGATGCTTCCAT[A/G]GGTGAGAAATAGCTT	314996
rs199265136	snp	A/G	0	0	intron-variant, missense	Klhl38	Rn_Celera	7:98192608	CTAAAATGCCAATCC[A/G]CTTTGATGCTCTCTC	314996
rs199286735	snp	A/T	0	0	intron-variant	Klhl38	Rn_Celera	7:98193968	ATGTACACACATTTG[A/T]ACATATATATGATTT	314996
rs199401575	snp	C/T	0	0	intron-variant	Klhl38	Rn_Celera	7:98189832	GTCAGTATCAGCAAC[C/T]GTTTCCCCTAAGGGA	314996

Full records

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