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
rs3691554	snp	A/G	0.444444	0.157135	utr-variant-5-prime, upstream-variant-2KB	Parp3, Rrp9	GRCm38.p3	9:106476834	TTTGACTAGGCACAT[A/G]CAGCATATATCCATT	27966
rs3720594	snp	A/G	0.5	0	synonymous-codon	Rrp9	GRCm38.p3	9:106480705	CCACAGCTTGGCTCC[A/G]AGGAAAACAGAGGAA	27966
rs6299195	snp	C/T	0.444444	0.157135	missense, upstream-variant-2KB	Parp3, Rrp9	GRCm38.p3	9:106475926	TCTGTCCCTTGTCGC[C/T]GCTTCTTGGAGCCCT	27966
rs13472712	snp	C/G	0.493827	0.0552116	synonymous-codon	Rrp9	GRCm38.p3	9:106481342	CAGGTTGCAGAAGTC[C/G]GTGGCCAAGGAGGTG	27966
rs29587274	snp	C/T	0.375	0.216506	intron-variant	Rrp9	GRCm38.p3	9:106479666	TTAGGGGTGAGGCTG[C/T]CTTGGTCTCCTGGCT	27966
rs29592276	snp	C/T	0.375	0.216506	intron-variant	Rrp9	GRCm38.p3	9:106484655	AGCCTGTCCCACTTT[C/T]CTCCTCTGTTCCCCA	27966
rs29694367	snp	C/T	0.32	0.24	intron-variant	Rrp9	GRCm38.p3	9:106481372	GAGTGTGCAGGGCAC[C/T]GTGGTGCGTGGGCAA	27966
rs29694727	snp	C/G	0.375	0.216506	intron-variant	Rrp9	GRCm38.p3	9:106479859	TGGAACCTAGTCCTC[C/G]GGGTACAAGGAGGGT	27966
rs29747320	snp	A/G	0.375	0.216506	intron-variant	Rrp9	GRCm38.p3	9:106482869	GTTGCTAAGCAGCTG[A/G]CCCTGCCCGCACCCT	27966
rs29791437	snp	C/T	0.375	0.216506	intron-variant	Rrp9	GRCm38.p3	9:106482867	AGGTTGCTAAGCAGC[C/T]GACCCTGCCCGCACC	27966
rs29795240	snp	G/T	0.375	0.216506	intron-variant	Rrp9	GRCm38.p3	9:106481527	GGCAGTGGTGGCGCA[G/T]GCCTTTAATCCCAGC	27966
rs29835025	snp	A/G	0.375	0.216506	intron-variant	Rrp9	GRCm38.p3	9:106479922	TCTGTGTCTTGGAGT[A/G]GTTGTCATCCTGGCA	27966
rs29842184	snp	A/G	0.375	0.216506	intron-variant	Rrp9	GRCm38.p3	9:106484989	TGGGAAAGGGTTGGC[A/G]CACCTAACCAGTGCA	27966
rs29892883	snp	C/T	0.375	0.216506	intron-variant	Rrp9	GRCm38.p3	9:106479903	CCTAGGGTACCCCAA[C/T]ATGTCTGTGTCTTGG	27966
rs29894526	snp	A/G	0.444444	0.157135	downstream-variant-500B	Rrp9	GRCm38.p3	9:106485535	TAGCTAGCTGCTCTC[A/G]GCTGAAGGCTTTTGT	27966
rs29936680	snp	A/G	0.375	0.216506	downstream-variant-500B	Rrp9	GRCm38.p3	9:106485633	CAGCCTAGAAACTAC[A/G]GCTCTCCATTCCTTG	27966
rs29946415	snp	A/G	0.375	0.216506	synonymous-codon	Rrp9	GRCm38.p3	9:106484020	CATGGTGTCGGGCGC[A/G]GATGATGGGTAAGAG	27966
rs30013842	snp	A/G	0.375	0.216506	intron-variant	Rrp9	GRCm38.p3	9:106481524	TAGGGCAGTGGTGGC[A/G]CATGCCTTTAATCCC	27966
rs30132109	snp	A/G	0.444444	0.157135	downstream-variant-500B	Rrp9	Mm_Celera	9:106485466	GGGTGAGGGGAGGGG[A/G]TAGGTGTGTGGCAAG	27966
rs30141001	snp	C/T	0.375	0.216506	upstream-variant-2KB, synonymous-codon	Parp3, Rrp9	GRCm38.p3	9:106477371	CGCCGTGGCAACTCG[C/T]AAGCGGGCAAAGCCA	27966
rs30172329	snp	C/T	0.375	0.216506	intron-variant	Rrp9	GRCm38.p3	9:106481924	GAGCCTGGGGTGGAG[C/T]CCTGATGGTGGAAGC	27966
rs30245404	snp	C/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Parp3, Rrp9	GRCm38.p3	9:106475698	CAGGACAGCCAGGGC[C/T]ATACAGAGAAACCCT	27966
rs30281883	snp	A/C	0.375	0.216506	intron-variant	Rrp9	GRCm38.p3	9:106479691	CTGGCTGAGAGTTCG[A/C]AACACCTACCTAAGC	27966
rs30287882	snp	A/G	0.375	0.216506	intron-variant	Rrp9	GRCm38.p3	9:106480207	ACAGTGCGGTTTTCT[A/G]GAGCATGGTGACTGA	27966
rs30331075	snp	C/T	0.375	0.216506	intron-variant	Rrp9	GRCm38.p3	9:106483723	CATGTGACCCTCCCT[C/T]CCTGCTTTGCTCTTC	27966
rs30353338	snp	A/G	0.375	0.216506	downstream-variant-500B	Rrp9	GRCm38.p3	9:106485605	TGACCTCATTAGACA[A/G]CTGCTCACCCATCAG	27966
rs30375758	snp	A/T	0.375	0.216506	intron-variant	Rrp9	GRCm38.p3	9:106479885	AGGGTGCAGGGCAGC[A/T]AGCCTAGGGTACCCC	27966
rs30505275	snp	A/G	0.375	0.216506	intron-variant	Rrp9	GRCm38.p3	9:106483062	GTTGGCCCTGTGGGC[A/G]GGTGGGAGGTTTGGG	27966
rs33628154	snp	A/T	0.375	0.216506	downstream-variant-500B	Rrp9	GRCm38.p3	9:106485623	GCTCACCCATCAGCC[A/T]AGAAACTACGGCTCT	27966
rs33724149	snp	C/G	0.375	0.216506	intron-variant	Rrp9	GRCm38.p3	9:106479675	AGGCTGCCTTGGTCT[C/G]CTGGCTGAGAGTTCG	27966
rs36634079	snp	C/G	0.375	0.216506	upstream-variant-2KB, intron-variant	Parp3, Rrp9	Mm_Celera	9:106477765	AGAGGTGAGTTTTTA[C/G]CGGGAGGAAGGATAA	27966
rs36756137	snp	A/C	0.21875	0.248039	intron-variant	Rrp9	GRCm38.p3	9:106483249	CCTGCCTAGCATGGA[A/C]GCCTGCTGGGTGTGC	27966
rs37152157	snp	C/T	0.231111	0.249285	intron-variant	Rrp9	Mm_Celera	9:106484053	CCTTTCTGATATGTC[C/T]GACTGCTGCCGCCAC	27966
rs37463900	snp	C/T	0.231111	0.249285	synonymous-codon	Rrp9	Mm_Celera	9:106484325	GGTGTCATCCGTAGC[C/T]GCCCTGCTCAATACA	27966
rs37614991	snp	A/G	0.124444	0.216185	intron-variant	Rrp9	Mm_Celera	9:106481127	GGCACTGCAGCCTGG[A/G]ATCATGTGGACCGTT	27966
rs45673602	snp	A/T			upstream-variant-2KB, intron-variant	Parp3, Rrp9	GRCm38.p3	9:106478202	TTCCTAACATTAGGG[A/T]CTTGTTTCACTGTTG	27966
rs45909138	snp	C/T			intron-variant	Rrp9	GRCm38.p3	9:106479245	AGAATTGCTAAATGC[C/T]GTTTATAAGGTCTCA	27966
rs45999618	snp	A/C			intron-variant	Rrp9	GRCm38.p3	9:106479660	TTGTGATTAGGGGTG[A/C]AGCTGTCTTGGTCTG	27966
rs46026191	snp	C/G			upstream-variant-2KB, intron-variant	Parp3, Rrp9	GRCm38.p3	9:106478035	AGAACACATCCTCCT[C/G]TTCTTAATTCCATCT	27966
rs46274770	snp	A/G			upstream-variant-2KB, intron-variant	Parp3, Rrp9	GRCm38.p3	9:106477997	AGGTCTGGATTGATT[A/G]AGAGGCAAGGAGAGA	27966
rs46286370	snp	G/T			intron-variant	Rrp9	GRCm38.p3	9:106479231	CAAAACAAAAAAGCA[G/T]AATTGCTAAATGCCG	27966
rs46407648	snp	C/T			intron-variant, upstream-variant-2KB, utr-variant-5-prime	Parp3, Rrp9	GRCm38.p3	9:106476210	CCCACGCTGGGGCCC[C/T]TCCCCTTCTAGAACA	27966
rs46585873	snp	A/G			upstream-variant-2KB, intron-variant	Parp3, Rrp9	GRCm38.p3	9:106478195	TGTAGCCTTCCTAAC[A/G]TTAGGGTCTTGTTTC	27966
rs46635268	snp	A/G			intron-variant	Rrp9	GRCm38.p3	9:106482131	CCTCACCTTCCCACC[A/G]TCCTCAGGGGGGTGG	27966
rs46793992	snp	A/G			utr-variant-5-prime, upstream-variant-2KB	Parp3, Rrp9	GRCm38.p3	9:106476519	AGGACCCTGGAAGAG[A/G]TGGCTGTTATCCAGC	27966
rs46857551	snp	C/G			intron-variant	Rrp9	Mm_Celera	9:106483339	GGTGTGTGTGTAAAG[C/G]CCGCGAGTGCGTTGA	27966
rs47024467	snp	C/T			upstream-variant-2KB, synonymous-codon	Parp3, Rrp9	GRCm38.p3	9:106477676	TGATTTCCAGGTAGA[C/T]TCTGCTGCGGACAGG	27966
rs47120305	snp	G/T			intron-variant	Rrp9	Mm_Celera	9:106481630	CCAGGGCTATTCAGA[G/T]AAACCCTGTCTCAAG	27966
rs47663797	snp	G/T			upstream-variant-2KB, synonymous-codon	Parp3, Rrp9	Mm_Celera	9:106477706	GGGCAAGTCCAAGGG[G/T]GGCGGCAAAATGAAT	27966
rs47703475	snp	A/G			intron-variant	Rrp9	GRCm38.p3	9:106479283	GTGTCTTTACCTGCT[A/G]AGCCGCCACACCTCT	27966
rs48599673	snp	C/T			upstream-variant-2KB, intron-variant	Parp3, Rrp9	GRCm38.p3	9:106477925	GGGAAGACGCTGGGC[C/T]CCTGTGGGAGGGAGA	27966
rs48797266	snp	A/T			upstream-variant-2KB, intron-variant	Parp3, Rrp9	GRCm38.p3	9:106477990	CAGGCACAGGTCTGG[A/T]TTGATTGAGAGGCAA	27966
rs49253576	snp	C/T			intron-variant	Rrp9	GRCm38.p3	9:106479766	GTGTCCTGAGCTGGC[C/T]CACGGACACTGGGGC	27966
rs49262986	snp	C/T			upstream-variant-2KB, intron-variant	Parp3, Rrp9	GRCm38.p3	9:106477569	ATCTCTTTTCTTCTA[C/T]CCACCAAATCCTGGG	27966
rs49402433	snp	A/C			upstream-variant-2KB, intron-variant	Parp3, Rrp9	GRCm38.p3	9:106477543	AAGGGCTCCGTCAGA[A/C]GGAAGCCTACATCTC	27966
rs50088285	snp	C/T			upstream-variant-2KB, intron-variant	Parp3, Rrp9	Mm_Celera	9:106477580	TCTATCCACCAAATC[C/T]TGGGAAACCTTCTAC	27966
rs50267377	snp	A/G			upstream-variant-2KB, intron-variant	Parp3, Rrp9	Mm_Celera	9:106477767	AGGTGAGTTTTTACC[A/G]GGAGGAAGGATAAAC	27966
rs50350553	snp	G/T			intron-variant, upstream-variant-2KB, utr-variant-5-prime	Parp3, Rrp9	GRCm38.p3	9:106476104	ATGCAGAAGCTTAGA[G/T]CCCGTCAGTTCTGCC	27966
rs51123745	snp	G/T			upstream-variant-2KB, intron-variant	Parp3, Rrp9	GRCm38.p3	9:106478107	TGAGATGAGGTCTCT[G/T]TTGTTTTGCCCAAGG	27966
rs51386127	snp	C/G			upstream-variant-2KB, intron-variant	Parp3, Rrp9	GRCm38.p3	9:106478194	ATGTAGCCTTCCTAA[C/G]ATTAGGGTCTTGTTT	27966
rs51786592	snp	C/T			intron-variant	Rrp9	GRCm38.p3	9:106479216	GGAAACAAAACAAAA[C/T]AAAACAAAAAAGCAG	27966
rs51961247	snp	C/T			intron-variant	Rrp9	Mm_Celera	9:106479765	AGTGTCCTGAGCTGG[C/T]TCACGGACACTGGGG	27966
rs52235743	snp	C/T			intron-variant	Rrp9	Mm_Celera	9:106482187	TTGTTGTTGTTGTTG[C/T]TGCTGTTGCTGCTGC	27966
rs52318994	snp	C/T			intron-variant	Rrp9	Mm_Celera	9:106482497	gccatctctccagcc[C/T]attattattattatt	27966
rs52444507	snp	C/T			intron-variant	Rrp9	GRCm38.p3	9:106482193	TTGTTGTTGTTGCTG[C/T]TGCTGCTGCTCCTCC	27966
rs52516030	snp	C/G			intron-variant	Rrp9	Mm_Celera	9:106482204	GCTGTTGCTGCTGCT[C/G]CTCCTCCTCTTCTTC	27966
rs52537497	snp	A/T			intron-variant	Rrp9	GRCm38.p3	9:106479157	AGGCAGACAGATCTG[A/T]GAGTTTGAGGCCAGC	27966
rs107741164	snp	A/C			intron-variant	Rrp9	Mm_Celera	9:106479186	GCCTGGGCTACGTGG[A/C]GAAAATATGTCTTGG	27966
rs108305738	snp	C/T			intron-variant	Rrp9	GRCm38.p3	9:106479124	CACACCTTTAATTCC[C/T]CAGTACCTAGGAGGC	27966
rs108477210	snp	A/G			upstream-variant-2KB, synonymous-codon	Parp3, Rrp9	GRCm38.p3	9:106477691	CTCTGCTGCGGACAG[A/G]GGCAAGTCCAAGGGT	27966
rs211797045	snp	A/G			intron-variant	Rrp9	Mm_Celera	9:106484064	TGTCCGACTGCTGCC[A/G]CCACCAGTGCTTCCT	27966
rs211947325	snp	G/T			intron-variant, upstream-variant-2KB	Parp3, Rrp9	Mm_Celera	9:106475690	ATGAGTTCCAGGACA[G/T]CCAGGGCCATACAGA	27966
rs212110850	snp	C/T			synonymous-codon	Rrp9	Mm_Celera	9:106481822	GCTCTCCATTACGTG[C/T]TTGGTCATCACTCCT	27966
rs212641964	in-del	-/G			intron-variant, upstream-variant-2KB	Parp3, Rrp9	Mm_Celera	9:106475616	TTAATCCCAGCACTT[-/G]GGAGACAGAGACAGG	27966
rs212861159	snp	A/G			upstream-variant-2KB, intron-variant	Parp3, Rrp9	Mm_Celera	9:106478460	CAGGCCAGGGTAGCC[A/G]TGAACTTAAGAGATC	27966
rs212866998	in-del	-/ACA			upstream-variant-2KB, intron-variant	Parp3, Rrp9	Mm_Celera	9:106478063	TCTTCACACAGTACC[-/ACA]ACGACTGGTGTCCTT	27966
rs212965725	in-del	-/TTTTTTT			upstream-variant-2KB, intron-variant	Parp3, Rrp9	Mm_Celera	9:106478567	CTTAATTTGCTCAGC[-/TTTTTTT]TTTTTTTTTTTTTTT	27966
rs213684771	snp	C/T			intron-variant	Rrp9	Mm_Celera	9:106482906	TCCCTCCTCGCTTCG[C/T]GGCAGGGAGTGTAGA	27966
rs213774795	snp	C/T			upstream-variant-2KB, intron-variant	Parp3, Rrp9	GRCm38.p3	9:106478284	TGTGTATCTTGGAGA[C/T]ATGTGTTGTGAGAAC	27966
rs214024912	snp	A/G			intron-variant	Rrp9	Mm_Celera	9:106482114	CCACACCTGAGCATA[A/G]TCCTCACCTTCCCAC	27966
rs214049115	in-del	-/A			intron-variant	Rrp9	GRCm38.p3	9:106481385	CCGTGGTGCGTGGGC[-/A]AGAGGCGGTGTGTGC	27966
rs214084123	snp	A/G			intron-variant	Rrp9	Mm_Celera	9:106484836	GTGACCTGTGGGGTT[A/G]TGTTATGATATGTCA	27966
rs214141915	snp	C/T			downstream-variant-500B	Rrp9	Mm_Celera	9:106485716	TTCAGGCTGACCACA[C/T]TTCCCTACTGTCCCA	27966
rs214368623	snp	C/T			intron-variant	Rrp9	Mm_Celera	9:106479960	TCTCTGTTCTGCATG[C/T]TGGGTTCCCTGTTTG	27966
rs214461137	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	Parp3, Rrp9	Mm_Celera	9:106476917	TGCCTGAATTCCATT[C/T]CTTAAGTTTTAGAGT	27966
rs214674623	in-del	-/GGGTCTACCCTCC			intron-variant	Rrp9	Mm_Celera	9:106483506	CAGGAGAGCCCCTCT[-/GGGTCTACCCTCC]GTAGTCCATACCCTT	27966
rs214995265	snp	C/G			upstream-variant-2KB, intron-variant	Parp3, Rrp9	Mm_Celera	9:106477888	CAGTGAGATATCGTC[C/G]TTTATCTCTGATGTG	27966
rs215261437	snp	C/T			intron-variant	Rrp9	Mm_Celera	9:106483944	GGGCTGGACGTTGCC[C/T]CCTCACAGCCTCTCT	27966
rs215648113	in-del	-/TTT			upstream-variant-2KB, intron-variant	Parp3, Rrp9	GRCm38.p3	9:106478568	CTTAATTTGCTCAGC[-/TTT]TTTTTTTTTTTTTTG	27966
rs215850947	snp	A/G			intron-variant, upstream-variant-2KB	Parp3, Rrp9	Mm_Celera	9:106475413	CCCGGGGGAAATTGA[A/G]TCAGGCCCCTTCCTT	27966
rs215976365	snp	C/T			intron-variant	Rrp9	Mm_Celera	9:106480840	AAGGCCAGGGTCTCC[C/T]GCAGAGCCTGCCTGC	27966
rs216380166	snp	A/G			downstream-variant-500B	Rrp9	Mm_Celera	9:106485877	CTTTTACAGATTGGG[A/G]ATTCTCTCCTGTTGT	27966
rs216595696	snp	A/G			intron-variant	Rrp9	Mm_Celera	9:106479291	ACCTGCTGAGCCGCC[A/G]CACCTCTAACTCTAG	27966
rs216754228	snp	G/T			intron-variant, upstream-variant-2KB, utr-variant-5-prime	Parp3, Rrp9	Mm_Celera	9:106476368	AGCCTTTTGCTAACA[G/T]TCCTGAGTTCTGGGG	27966
rs217698264	snp	G/T			intron-variant	Rrp9	Mm_Celera	9:106479389	AACTCTGGGCCAAGG[G/T]CTGGCCTTGACTTTC	27966
rs217831029	in-del	-/T			intron-variant	Rrp9	Mm_Celera	9:106481748	CAGTGATGCAGTCTC[-/T]TGTCTTTCCAGATCC	27966
rs217959264	snp	C/G			upstream-variant-2KB, intron-variant	Parp3, Rrp9	Mm_Celera	9:106478454	TAGGTACAGGCCAGG[C/G]TAGCCGTGAACTTAA	27966
rs219001891	snp	C/G			upstream-variant-2KB, intron-variant	Parp3, Rrp9	Mm_Celera	9:106478406	GTATTAGTGTGCCAG[C/G]GTGGAAGGAAGAAAG	27966
rs219692690	snp	C/T			intron-variant	Rrp9	Mm_Celera	9:106483289	GCCAGGCGCCAGGCC[C/T]CAGGCTCATCTACAG	27966
rs219815114	snp	C/T			intron-variant	Rrp9	Mm_Celera	9:106484109	GGACTTAGCTCATTT[C/T]GGATCAGTGGCCACA	27966

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