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
rs3677280	snp	G/T	0.444444	0.157135	utr-variant-5-prime, intron-variant	Gm12657, Plaa	Mm_Celera	4:94599358	CAGCTGAAGGAGAAG[G/T]GGGGTAAGTAAGGAG	18786
rs3725734	snp	C/G	0.5	0	intron-variant	Gm12657, Plaa	Mm_Celera	4:94594812	TTGAGGGTGGCCTTC[C/G]AGGTTTCAAAAGCCA	18786
rs13460736	snp	A/C			synonymous-codon, upstream-variant-2KB	Plaa, Ift74	GRCm38.p3	4:94602984	GCTGAGCTGCTCGCT[A/C]CCGGGCCACGAACTG	18786
rs13460737	snp	C/T			synonymous-codon	Plaa	Mm_Celera	4:94582575	AAATGATTTGAATCC[C/T]ATGTTTCTGGATCAG	18786
rs13460738	snp	G/T	0.260355	0.249785	synonymous-codon, missense	Plaa	Mm_Celera	4:94586321	TTGCTGCGTACTGGA[G/T]AATGGTGACATTGTG	18786
rs13460739	snp	A/G			stop-gained, missense	Plaa	Mm_Celera	4:94586336	TCAGTCTATATGGTG[A/G]TGCTGCGTACTGGAA	18786
rs28157342	snp	C/T	0.345679	0.230967	intron-variant	Gm12657, Plaa	Mm_Celera	4:94598264	TCTGGAGGAAGCAGA[C/T]CACCAAGAAGAAAAG	18786
rs28157343	snp	A/G	0.124444	0.216185	intron-variant	Gm12657, Plaa	Mm_Celera	4:94598039	AAAAACAAAACACCC[A/G]AGGCCAGGCCAGTAG	18786
rs28157344	snp	C/T	0.32	0.24	intron-variant	Gm12657, Plaa	Mm_Celera	4:94598038	AAAAAACAAAACACC[C/T]GAGGCCAGGCCAGTA	18786
rs28157345	snp	A/G	0.497778	0.0332592	intron-variant	Gm12657, Plaa	Mm_Celera	4:94598008	GGACATTTACATCAC[A/G]GTCCAAGATCATAAA	18786
rs28157346	snp	C/T	0.375	0.216506	intron-variant	Gm12657, Plaa	Mm_Celera	4:94597871	AGGGAGACAGCGGCC[C/T]TCTTCTGGCCCTCTT	18786
rs28157347	snp	G/T	0.32	0.24	intron-variant	Gm12657, Plaa	Mm_Celera	4:94595957	CAGCTGGAAGGTTTC[G/T]ATTCCCAGCTTTTCT	18786
rs28157348	snp	C/G	0.32	0.24	intron-variant	Gm12657, Plaa	GRCm38.p3	4:94595888	TTTACACAAAGTCCT[C/G]TTAGACAAGAGTGTT	18786
rs28157349	snp	A/G	0.32	0.24	intron-variant	Gm12657, Plaa	Mm_Celera	4:94595779	GGAGGACCAACTGGA[A/G]TCCTCAGTCCTGCAC	18786
rs28157350	snp	A/G	0.32	0.24	intron-variant	Gm12657, Plaa	Mm_Celera	4:94595751	ACACTCAGCAGAGAG[A/G]AGTGAGATTTATGGA	18786
rs28157351	snp	A/C	0.124444	0.216185	intron-variant	Gm12657, Plaa	Mm_Celera	4:94595582	AATAGCACCAAAAAA[A/C]CAGACCTTTGTAAGA	18786
rs28157352	snp	A/G	0.124444	0.216185	upstream-variant-2KB, intron-variant	Gm12657, Plaa	Mm_Celera	4:94593625	AGAGAATAAGCCAAG[A/G]GTCTGGGGTACAGTT	18786
rs28157353	snp	A/C	0.260355	0.249785	upstream-variant-2KB, intron-variant	Gm12657, Plaa	Mm_Celera	4:94593592	TCAATATCCCACCCA[A/C]TAACAGGATGACAAC	18786
rs28157354	snp	C/T	0.124444	0.216185	upstream-variant-2KB, intron-variant	Gm12657, Plaa	Mm_Celera	4:94593590	CCTCAATATCCCACC[C/T]AATAACAGGATGACA	18786
rs28157355	snp	A/G	0.32	0.24	upstream-variant-2KB, intron-variant	Gm12657, Plaa	Mm_Celera	4:94593410	AGCAAGTTGCAGGCT[A/G]GGTCACCCTAGGTTA	18786
rs28157356	snp	G/T	0.124444	0.216185	upstream-variant-2KB, intron-variant	Gm12657, Plaa	Mm_Celera	4:94593386	ATGTTGATATATGCC[G/T]GTGATTCCAGCAAGT	18786
rs28157357	snp	A/G	0.32	0.24	upstream-variant-2KB, intron-variant	Gm12657, Plaa	Mm_Celera	4:94592801	TTTTCCATATGAAAT[A/G]AATTCAGAGTCAGGC	18786
rs28157358	snp	A/C	0.32	0.24	upstream-variant-2KB, intron-variant	Gm12657, Plaa	GRCm38.p3	4:94592431	CACAAACCTTATTCA[A/C]GATACCAGGCAAATT	18786
rs28157359	snp	A/G	0.124444	0.216185	intron-variant	Plaa	Mm_Celera	4:94591613	AGAGGCTGTCTCAAA[A/G]TACAAACGGCCTTAA	18786
rs28157360	snp	A/G	0.124444	0.216185	intron-variant	Plaa	Mm_Celera	4:94591596	GCTTTGGCTACACAG[A/G]TAGAGGCTGTCTCAA	18786
rs28157361	snp	C/T	0.32	0.24	intron-variant	Plaa	Mm_Celera	4:94590383	CACCACTTTTCTACT[C/T]ATCAGGTATTGCTGC	18786
rs28157362	snp	C/T	0.132653	0.220748	intron-variant	Plaa	Mm_Celera	4:94590104	TCATTAATACAAACA[C/T]ACTTGGCCCCTGGCT	18786
rs28157363	snp	A/G	0.489796	0.070696	intron-variant	Plaa	Mm_Celera	4:94588908	TCAAGAGCCCATAAA[A/G]AAAGATTATTTGTTG	18786
rs28157364	snp	A/G	0.132653	0.220748	intron-variant	Plaa	Mm_Celera	4:94588899	GTACACATTTCAAGA[A/G]CCCATAAAGAAAGAT	18786
rs28157365	snp	C/T	0.35503	0.226867	intron-variant	Plaa	Mm_Celera	4:94588785	ATTAATGCATACAAA[C/T]CACTTGTTTTTTCAC	18786
rs28157366	snp	A/C	0.32	0.24	intron-variant	Plaa	Mm_Celera	4:94588702	CAGCAGTCGAGGAAC[A/C]ACACCCAAGGCTGTC	18786
rs28157367	snp	A/G	0.152778	0.230321	intron-variant	Plaa	Mm_Celera	4:94587716	ATAGAGCTCTACTCA[A/G]TGGAACTGCAAGAGA	18786
rs28157368	snp	G/T	0.46875	0.121031	intron-variant	Plaa	GRCm38.p3	4:94587691	GTCTGTGAAGTGATG[G/T]TTTTAGCCAATAGAG	18786
rs28157369	snp	C/T	0.46281	0.131194	intron-variant	Plaa	Mm_Celera	4:94587475	TCTAAAATATTCACA[C/T]AAAAACAATACCTGT	18786
rs28157370	snp	C/T	0.336735	0.234472	intron-variant	Plaa	Mm_Celera	4:94587135	TTACATGCATTACAA[C/T]ACACACAAAATCAGA	18786
rs28157371	snp	A/G	0.336735	0.234472	intron-variant	Plaa	Mm_Celera	4:94586985	CTCTGCAGCTTATTA[A/G]CACCATAAAACTTGT	18786
rs28157372	snp	A/T	0.260355	0.249785	synonymous-codon	Plaa	Mm_Celera	4:94586393	TTCACCATGTTTCCA[A/T]ATTCTTAGAGATCTG	18786
rs28157373	snp	A/T	0.132653	0.220748	intron-variant	Plaa	GRCm38.p3	4:94585956	ATCTTACTCCAGTAC[A/T]TCCCTAATCTAAACA	18786
rs28157374	snp	A/G	0.336735	0.234472	intron-variant	Plaa	Mm_Celera	4:94585794	ATCCATTAGTGTTGT[A/G]AGGTCAGTGTTACCT	18786
rs28157375	snp	A/G	0.132653	0.220748	intron-variant	Plaa	Mm_Celera	4:94585329	ACTGGCTAGTCTTCC[A/G]TCTCTCTTCTACACT	18786
rs28157376	snp	C/T	0.336735	0.234472	intron-variant	Plaa	Mm_Celera	4:94585181	CATTCTCGGACCACT[C/T]AGCATTCTATGACAC	18786
rs28157377	snp	A/T	0.260355	0.249785	intron-variant	Plaa	Mm_Celera	4:94585034	TCTGTTCCCAATGTC[A/T]AGTTTACAATCTCTT	18786
rs28157378	snp	G/T	0.244898	0.249948	intron-variant	Plaa	Mm_Celera	4:94584972	TGCCACAACCATAAA[G/T]AAGAGGTCTACCAAA	18786
rs28157379	snp	A/G	0.336735	0.234472	intron-variant	Plaa	Mm_Celera	4:94583717	AGGACTAATCCTCAA[A/G]TATCAGTACCTGGCA	18786
rs28157380	snp	A/G	0.5	0	intron-variant	Plaa	GRCm38.p3	4:94582904	TAGTTGTTTCATTAC[A/G]AATGGGGCAGGTGAT	18786
rs28157381	snp	A/G	0.336735	0.234472	intron-variant	Plaa	Mm_Celera	4:94582887	TGCATGTGCTGCAAA[A/G]TTAGTTGTTTCATTA	18786
rs28157382	snp	A/G	0.408163	0.193609	intron-variant	Plaa	Mm_Celera	4:94582398	ACATGATATTGATTA[A/G]TATCTCCACTAAAAC	18786
rs28157383	snp	C/T	0.132653	0.220748	intron-variant	Plaa	Mm_Celera	4:94582337	GATGAGAAAAATTGG[C/T]TAGGGCTGGGTTATA	18786
rs28157384	snp	C/T	0.260355	0.249785	intron-variant	Plaa	Mm_Celera	4:94582206	TCTGGGCAGAGTGTA[C/T]TGTAATTGTTTCTGT	18786
rs28157385	snp	A/T	0.132653	0.220748	intron-variant	Plaa	Mm_Celera	4:94580891	TACAGGCAACGGAAT[A/T]CAAATCACATGTTCA	18786
rs28157386	snp	G/T	0.260355	0.249785	intron-variant	Plaa	Mm_Celera	4:94580451	TGGCTACTAGAATGT[G/T]CAAGGCCTTCCCTGA	18786
rs28157387	snp	A/C	0.132653	0.220748	intron-variant	Plaa	Mm_Celera	4:94578376	TCATATTAATGAAAA[A/C]TGCATCCCACCTGTG	18786
rs28157388	snp	A/G	0.260355	0.249785	intron-variant	Plaa	Mm_Celera	4:94577009	AACCACTTGCATTTC[A/G]GTGATCACATTATTC	18786
rs28157389	snp	C/T	0.492188	0.0620098	intron-variant	Plaa	Mm_Celera	4:94576706	TGGTAATGATGGACC[C/T]AGAAGTTCTCCTGAT	18786
rs28157390	snp	C/T	0.396694	0.202437	intron-variant	Plaa	Mm_Celera	4:94576459	GGTAGGATACTGCCA[C/T]TTTGATGTTCTTGTT	18786
rs28157391	snp	A/G	0.375	0.216506	intron-variant	Plaa	Mm_Celera	4:94575861	CTTAAACATGTGTCT[A/G]GGATGCTCTGACAAC	18786
rs28157392	snp	C/T	0.244898	0.249948	intron-variant	Plaa	Mm_Celera	4:94573609	TTTGTACAAAGCTTC[C/T]TAGAATCCATTAAGG	18786
rs28157393	snp	C/T	0.444444	0.157135	intron-variant	Plaa	GRCm38.p3	4:94573559	AGCTTGAGGGCAGGA[C/T]TTTCATTGTTTTATT	18786
rs28157394	snp	C/T	0.489796	0.070696	intron-variant	Plaa	Mm_Celera	4:94572729	TTAAACTCTTCCTGC[C/T]TCACCTCCTAAATGC	18786
rs28157395	snp	C/T	0.5	0	intron-variant	Plaa	Mm_Celera	4:94571590	CTAGTGATGTGGCAA[C/T]GCCTTTCTGTGCAAC	18786
rs28157396	snp	A/G	0.5	0	intron-variant	Plaa	GRCm38.p3	4:94570848	CGAGTCTAAGAAAAT[A/G]GGACATTACGTGCTT	18786
rs28157397	snp	G/T	0.48	0.0979796	utr-variant-3-prime	Plaa	Mm_Celera	4:94565790	TATAGCTTTAAGTCC[G/T]TAGAGGGTCACTGAA	18786
rs28157398	snp	C/T	0.244898	0.249948	utr-variant-3-prime	Plaa	Mm_Celera	4:94565760	AGAGATTTAACTCCA[C/T]GTCAAGGAGCACTGT	18786
rs31768758	snp	C/T	0.444444	0.157135	intron-variant	Plaa	Mm_Celera	4:94586104	CTCTATTTTTTCTAA[C/T]TTCTTTGGTATTCAG	18786
rs31775835	snp	C/T	0.375	0.216506	utr-variant-3-prime	Plaa	GRCm38.p3	4:94566771	GGGACATCACGTATG[C/T]CTGTAGTTGAATGTA	18786
rs31782919	snp	A/G	0.444444	0.157135	intron-variant	Gm12657, Plaa	Mm_Celera	4:94598354	ACCACAAACCAGAAT[A/G]TAAGTTCAAGTCAAC	18786
rs31922259	snp	C/T	0.5	0	upstream-variant-2KB, intron-variant	Gm12657, Plaa	Mm_Celera	4:94591966	GAATGCCTAAAAACA[C/T]GAGTTCAATCACACA	18786
rs31947601	snp	C/T	0.444444	0.157135	intron-variant	Plaa	Mm_Celera	4:94581546	TTTTATTTAATTTAT[C/T]GGGAGGTTATTTTTA	18786
rs31948799	snp	A/T	0.375	0.216506	downstream-variant-500B, intron-variant	Gm12657, Plaa	GRCm38.p3	4:94600468	GGTAACACTAATTTC[A/T]AATGTTCCCTAGCAG	18786
rs31984987	snp	A/G	0.375	0.216506	intron-variant	Plaa	Mm_Celera	4:94588755	ATTGTTTAGTGGGGG[A/G]AAAAAAATCAGCAAA	18786
rs32052265	snp	A/G	0.444444	0.157135	upstream-variant-2KB, intron-variant	Plaa, Ift74	GRCm38.p3	4:94604992	ACATATTTGTATAGC[A/G]ATCATTTCTGCAAGA	18786
rs32129015	snp	A/C	0.444444	0.157135	intron-variant, upstream-variant-2KB	Plaa, Ift74	Mm_Celera	4:94601876	CTAATAAGAGATATC[A/C]GCTTCAACACACACA	18786
rs32140173	snp	C/T	0.444444	0.157135	intron-variant	Gm12657, Plaa	Mm_Celera	4:94598353	AACCACAAACCAGAA[C/T]GTAAGTTCAAGTCAA	18786
rs32161906	snp	C/T	0.444444	0.157135	intron-variant	Plaa	Mm_Celera	4:94576412	AAAAACCTTTATATG[C/T]ATTATGCCACTTAAT	18786
rs32171757	snp	A/G	0.444444	0.157135	intron-variant	Plaa	Mm_Celera	4:94584525	TGGGCATTGGGGAAC[A/G]TACAATGAGCCTGAG	18786
rs32203925	snp	G/T	0.444444	0.157135	intron-variant	Plaa	Mm_Celera	4:94582773	ATATAGCATAATATA[G/T]ATGGTATGCGGTCTT	18786
rs32223811	snp	C/G	0.375	0.216506	intron-variant	Gm12657, Plaa	Mm_Celera	4:94599329	TGCCACAGCCGCTCT[C/G]CAACGCCGAGCTCCA	18786
rs32270190	snp	C/T	0.444444	0.157135	intron-variant	Gm12657, Plaa	Mm_Celera	4:94593832	TTAAAACACAACCAC[C/T]ATATGATCTAGCAAT	18786
rs32289827	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Plaa, Ift74	Mm_Celera	4:94602661	AGTTAGGACAGCCAG[C/T]CAGGTCCTCCAATCC	18786
rs32319507	snp	A/G	0.5	0	upstream-variant-2KB, intron-variant	Plaa, Ift74	GRCm38.p3	4:94604265	TTATTTCATGAATGT[A/G]GGTATACTGTCGCTG	18786
rs32346354	snp	C/T	0.444444	0.157135	upstream-variant-2KB, utr-variant-5-prime, intron-variant	Plaa, Ift74	Mm_Celera	4:94603883	TAGCTCGGGCTAGCC[C/T]AAAACTCGTGGTTCC	18786
rs32350043	snp	A/G	0.444444	0.157135	intron-variant	Gm12657, Plaa	Mm_Celera	4:94595702	TCTTTTCTTCCCCCC[A/G]CCACAGCTCTCATCC	18786
rs32366988	snp	G/T	0.444444	0.157135	intron-variant	Plaa	Mm_Celera	4:94576808	TAATTATGGAATTCT[G/T]CTGGACTGAATTTCA	18786
rs32385670	snp	A/G	0.375	0.216506	intron-variant	Gm12657, Plaa	Mm_Celera	4:94598748	TAGCAAGACAGAAAA[A/G]AAAATGTTTTCAAAC	18786
rs32394650	snp	A/G/T	0.375	0.216506	utr-variant-3-prime, intron-variant	Gm12657, Plaa	GRCm38.p3	4:94600312	TAAACTATATATATA[A/G/T]AAAAAGATAAATACA	18786
rs32410460	snp	G/T	0.5	0	utr-variant-3-prime	Plaa	Mm_Celera	4:94568700	AATGAAGTTACCTCA[G/T]ATAGTGAAAGAAACT	18786
rs32423243	snp	A/T	0.375	0.216506	intron-variant	Plaa	Mm_Celera	4:94586571	AAATCATGTTTTTAT[A/T]CATTTCACATCATAC	18786
rs32449465	snp	A/G	0.444444	0.157135	intron-variant	Plaa	GRCm38.p3	4:94591177	ATCCAGCCTACTGAA[A/G]CTAATTTTACTCAAT	18786
rs32466164	snp	C/T	0.444444	0.157135	intron-variant	Plaa	GRCm38.p3	4:94585607	GGGATTAAAGGCGTT[C/T]GCCACCATTGCCTGG	18786
rs32509163	snp	C/T	0.375	0.216506	intron-variant	Plaa	Mm_Celera	4:94589393	CATATTTATTTAGAA[C/T]TCACTCTAAAATACC	18786
rs32557257	snp	C/T	0.375	0.216506	intron-variant	Gm12657, Plaa	Mm_Celera	4:94599347	ACGCCGAGCTCCAGC[C/T]GAAGGAGAAGTGGGG	18786
rs32586086	snp	C/T	0.5	0	upstream-variant-2KB, intron-variant	Plaa, Ift74	GRCm38.p3	4:94604826	CATATACACATACCC[C/T]TCAACAAGCACACAC	18786
rs32589756	snp	A/G	0.444444	0.157135	upstream-variant-2KB, utr-variant-5-prime, intron-variant	Plaa, Ift74	GRCm38.p3	4:94603585	TTGCTTGTTTGCCTT[A/G]CGCCACGATTTGTTT	18786
rs32706270	snp	A/G	0.5	0	intron-variant	Gm12657, Plaa	GRCm38.p3	4:94599324	TGCCGTGCCACAGCC[A/G]CTCTGCAACGCCGAG	18786
rs32731005	snp	C/T	0.375	0.216506	utr-variant-3-prime, intron-variant	Gm12657, Plaa	Mm_Celera	4:94600209	CATCCATTCACTATA[C/T]TTTTCTGAGTTGTCC	18786
rs32736647	snp	C/T	0.5	0	intron-variant	Gm12657, Plaa	Mm_Celera	4:94597370	TGCCCAAGAGAGGTA[C/T]TGCGGGATCCTCCGG	18786
rs32746192	snp	C/G	0.444444	0.157135	upstream-variant-2KB, intron-variant	Plaa, Ift74	GRCm38.p3	4:94604073	ACAAACCTTTGTTAA[C/G]TTGCCAAATCCAATT	18786
rs32799260	snp	A/G	0.375	0.216506	intron-variant	Plaa	Mm_Celera	4:94574881	ATAATATTTAGTGGA[A/G]TAAAATGACTTTAAA	18786
rs32806130	snp	C/T	0.444444	0.157135	intron-variant	Plaa	Mm_Celera	4:94586031	CAGAAATTCTAATTT[C/T]CATTATTCAACTTTG	18786
rs32868975	snp	C/T	0.375	0.216506	upstream-variant-2KB, intron-variant	Gm12657, Plaa	Mm_Celera	4:94591723	AAAAAGATCTAAGTG[C/T]ACACATCAAGTATAC	18786

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