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
rs8143271	snp	A/G	0	0	downstream-variant-500B	Ccnf	Rn_Celera	10:13594408	ACTTGTGGCTCAGGG[A/G]TATCTGGGGCACTCA	117524
rs8153530	snp	A/G			synonymous-codon	Ccnf	Rn_Celera	10:13610194	AGAATCTGCTCATCA[A/G]GGATGCTTGGCCAGC	117524
rs104950165	snp	C/G	0	0	intron-variant	Ccnf	Rn_Celera	10:13616013	AGGAGGCACGCACGC[C/G]TCACACTTATGGATA	117524
rs105322535	snp	A/G	0	0	intron-variant	Ccnf	Rn_Celera	10:13612232	ACAACGATGAACTTC[A/G]CATAGTGTAGGTAGA	117524
rs105429166	snp	A/C	0.375	0.216506	intron-variant	Ccnf	Rn_Celera	10:13618625	TATGTGGGTATGACT[A/C]AAAGTATACCATTGA	117524
rs105461923	snp	C/T	0	0	intron-variant	Ccnf	Rn_Celera	10:13605111	GGTTTCTGGGCTGCT[C/T]GGCGCCATCAGCCAC	117524
rs105556114	snp	C/G	0	0	intron-variant	Ccnf	Rn_Celera	10:13597031	CAACTGGAAGAAGAA[C/G]TGGGTGAGGCCAGGC	117524
rs105588654	snp	A/T	0	0	intron-variant	Ccnf	Rn_Celera	10:13608338	CTCACACGTCACTCG[A/T]GACAAACAGGAACTA	117524
rs106278748	snp	C/T	0	0	intron-variant	Ccnf	Rn_Celera	10:13604858	TCATCATTTTGAAAC[C/T]ACTGATTTACCAATT	117524
rs106335161	snp	C/T	0.5	0	intron-variant	Ccnf	Rn_Celera	10:13609932	CACTCCTGAGCTGCA[C/T]TGGCCTCCCCAACCT	117524
rs106387639	snp	C/T	0	0	intron-variant	Ccnf	Rn_Celera	10:13618194	GGAGAGATGGCTCAG[C/T]GGTTAAGAGCACTGA	117524
rs106482308	snp	A/C	0.375	0.216506	intron-variant	Ccnf	Rn_Celera	10:13618503	TCAGGCTGGCCTAAA[A/C]TTCACTAATGTAGCT	117524
rs106732833	snp	A/G	0	0	intron-variant	Ccnf	Rn_Celera	10:13614923	TGAGGGCTACAGAGA[A/G]AATCCACGACACTTT	117524
rs106834848	snp	A/G	0	0	intron-variant	Ccnf	Rn_Celera	10:13613030	CCTAAGGCAGTGAGA[A/G]CACAAACGACATCAC	117524
rs106905405	snp	A/G	0.5	0	intron-variant	Ccnf	Rn_Celera	10:13612905	AGGGCTGAAGCTTCT[A/G]CTTAACTCAAATACC	117524
rs106934944	snp	A/G	0	0	intron-variant	Ccnf	Rn_Celera	10:13617369	ATGCCCTCTTCTGGT[A/G]TGTGTGAAGACAGCC	117524
rs106966927	snp	C/T	0.5	0	intron-variant	Ccnf	Rn_Celera	10:13615732	ACTTTCCAGGTCTCC[C/T]TAGTGTCATTCCTTG	117524
rs107076993	snp	A/C	0.375	0.216506	intron-variant	Ccnf	Rn_Celera	10:13618394	CTTGGGGACCGAGAA[A/C]TGGCACAGCAGTGAA	117524
rs107103930	snp	A/G	0	0	intron-variant	Ccnf	Rn_Celera	10:13611981	GCTCTGAGGGCTGGG[A/G]CTCCAATTCTCCTGG	117524
rs107128530	snp	C/T	0.375	0.216506	intron-variant	Ccnf	Rn_Celera	10:13618449	AGATCCCTCGGACTT[C/T]TGCTGTATGTGTCTG	117524
rs107189592	snp	C/T	0.5	0	intron-variant	Ccnf	Rn_Celera	10:13618308	TCTAGGCTGCAGGTA[C/T]ACAGCCCAGAATTAT	117524
rs107277872	snp	C/T	0.375	0.216506	intron-variant	Ccnf	Rn_Celera	10:13618573	GCCAAGTACTGAATT[C/T]TAAGTGTTAGCCACC	117524
rs107284161	snp	A/G	0	0	synonymous-codon	Ccnf	Rn_Celera	10:13598219	TTTGCTTCTCCTCCC[A/G]GAGGGTGAGCTGAGG	117524
rs107296484	snp	A/G	0	0	intron-variant	Ccnf	Rn_Celera	10:13602233	TTCCTGAACCCACAT[A/G]GTGGAAGGAGGACCA	117524
rs107576294	snp	G/T	0	0	intron-variant	Ccnf	Rn_Celera	10:13613191	ACCCTTTTGCCAATC[G/T]CGAAAGGTCAAGTAT	117524
rs197039589	snp	A/C	0	0	intron-variant	Ccnf	Rn_Celera	10:13604892	CATAACCCACGGAAA[A/C]TCCCGGGAGGCTGGT	117524
rs197189106	snp	A/T	0	0	intron-variant	Ccnf	Rn_Celera	10:13611293	CCCCCGATTCCCTGT[A/T]TCTGACTCTGTCTGA	117524
rs197207444	snp	C/T	0	0	intron-variant	Ccnf	Rn_Celera	10:13614094	CACTAGCCAGCACAC[C/T]GATACCACAAAGGCT	117524
rs197329663	snp	A/C	0	0	intron-variant	Ccnf	Rn_Celera	10:13617000	TGGCTATTGGCTGTT[A/C]ATCCAGAGGCCCTGG	117524
rs197588549	snp	C/T	0	0	intron-variant	Ccnf	Rn_Celera	10:13604474	ACTTAAATTATTGTA[C/T]TAACACAATTGAAAC	117524
rs197795772	snp	G/T	0	0	intron-variant	Ccnf	Rn_Celera	10:13611158	TTCTCTGTGTCTCGG[G/T]CTGTCTCTCTCTCTC	117524
rs198096269	snp	A/G	0	0	utr-variant-3-prime	Ccnf	Rn_Celera	10:13595222	GCTGAAGGGGTGAGG[A/G]GGGACAGTGCTGTGT	117524
rs198161063	snp	A/T	0	0	intron-variant	Ccnf	Rnor_6.0	10:13611360	CCCCGTTTCTCTCTG[A/T]GTCTCTGTCTCTCTG	117524
rs198401343	snp	A/T	0	0	intron-variant	Ccnf	Rn_Celera	10:13611221	CCCCTGTTCCTCTGT[A/T]TCTCTGTCTGTCTCT	117524
rs198837653	snp	A/G	0	0	intron-variant	Ccnf	Rn_Celera	10:13604034	CAGCAGACAGCAGAC[A/G]GTCTACACACAGCCC	117524
rs199088282	snp	A/T	0	0	intron-variant	Ccnf	Rnor_6.0	10:13611376	GTCTCTGTCTCTCTG[A/T]ATCTCTGCCTCCCCC	117524
rs199410058	snp	C/T	0	0	intron-variant	Ccnf	Rn_Celera	10:13601539	ATCTATCTCCACACG[C/T]ACACATGTGCTCACA	117524

Full records

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