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
rs8239772	snp	A/G	0.18	0.24	intron-variant	Gnb5	GRCm38.p3	9:75327797	TGAGACCTTAGTTAA[A/G]AAGAAACGACCACAA	14697
rs8239773	snp	A/G	0.18	0.24	intron-variant	Gnb5	GRCm38.p3	9:75327780	AGAAACGACCACAAC[A/G]AAACCAGACAAAAAC	14697
rs8239774	snp	C/T	0.18	0.24	intron-variant	Gnb5	GRCm38.p3	9:75327765	AAAACCAGACAAAAA[C/T]TAAAAAGCAAAAATA	14697
rs8239775	in-del	-/TA	0.5	0	intron-variant	Gnb5	GRCm38.p3	9:75327709	ATATTAAAAGAAAAA[-/TA]NAAAAGCCATTNNTG	14697
rs8239776	in-del	-/A	0.493827	0.0552116	intron-variant	Gnb5	Mm_Celera	9:75327710	TATTAAAAGAAAAAN[-/A]AAAAGCCATTNNTGG	14697
rs8239777	snp	A/C	0.18	0.24	intron-variant	Gnb5	GRCm38.p3	9:75327699	AAAAAAAAAGCCATT[A/C]ATGGAATTTCAATCA	14697
rs8239778	snp	A/G	0.475309	0.108333	intron-variant	Gnb5	GRCm38.p3	9:75327698	AAAAAAAAGCCATTC[A/G]TGGAATTTCAATCAT	14697
rs8239779	snp	A/G	0.21875	0.248039	intron-variant	Gnb5	GRCm38.p3	9:75327679	AATTTCAATCATTAC[A/G]CCCTGCTGGAGGTAG	14697
rs8239780	snp	C/T	0.226843	0.248925	intron-variant	Gnb5	GRCm38.p3	9:75327675	TCAATCATTACGCCC[C/T]GCTGGAGGTAGGGAA	14697
rs8239781	in-del	-/G	0.644636	0.0747315	intron-variant	Gnb5	Mm_Celera	9:75327629	TCCTTCACAAATNNN[-/G]CCTTGTAANNNNAGA	14697
rs8254952	snp	A/G	0.345679	0.230967	intron-variant	Gnb5	Mm_Celera	9:75327341	TCAGGCGGCGAAGGA[A/G]GAAAGAGCCGTCCTG	14697
rs8254953	snp	A/G	0.453686	0.144955	intron-variant	Gnb5	Mm_Celera	9:75327436	ATTCTCCTGCAATGT[A/G]GAAGTATATGGCAGT	14697
rs8254954	snp	C/T	0.491493	0.0646602	intron-variant	Gnb5	Mm_Celera	9:75327448	TGTGGAAGTATATGG[C/T]AGTGTTTGCGCCCTT	14697
rs8254955	snp	A/T	0.486111	0.0821678	intron-variant	Gnb5	Mm_Celera	9:75327455	GTATATGGCAGTGTT[A/T]GCGCCCTTGTCTGAC	14697
rs8254956	snp	A/G	0.15879	0.232768	intron-variant	Gnb5	Mm_Celera	9:75327458	TATGGCAGTGTTTGC[A/G]CCCTTGTCTGACACG	14697
rs8254957	snp	C/T	0.15879	0.232768	intron-variant	Gnb5	Mm_Celera	9:75327472	CGCCCTTGTCTGACA[C/T]GCACTGTGCCTTGGG	14697
rs8254958	snp	A/C	0.496528	0.0415217	intron-variant	Gnb5	Mm_Celera	9:75327489	CACTGTGCCTTGGGG[A/C]TGACCCCAGCACTGG	14697
rs8259460	snp	A/C	0.497041	0.0383476	intron-variant	Gnb5	Mm_Celera	9:75327536	CACCCTGGAGAATGT[A/C]ACTGATCTCGAATTA	14697
rs8259461	snp	C/T	0.48	0.0979796	intron-variant	Gnb5	GRCm38.p3	9:75327585	TGGATTGTGTCTGAC[C/T]NCCTTTGATGANNNN	14697
rs8259462	in-del	-/C	0.345679	0.230967	intron-variant	Gnb5	GRCm38.p3	9:75327586	GGATTGTGTCTGACN[-/C]CCTTTGATGANNNNN	14697
rs8259473	in-del	-/C	0.64	0.08	intron-variant	Gnb5	Mm_Celera	9:75327630	CTNNNNTTACAAGGN[-/C]NNATTTGTGAAGGAA	14697
rs8260621	snp	A/T	0.48	0.0979796	intron-variant	Gnb5	Mm_Celera	9:75328050	ACCTCAATTTTGGAG[A/T]AATGTGTTATGCAGC	14697
rs8260622	snp	A/G	0.165289	0.235211	intron-variant	Gnb5	GRCm38.p3	9:75328046	CAATTTTGGAGTAAT[A/G]TGTTATGCAGCAATA	14697
rs8260623	snp	G/T	0.152778	0.230321	intron-variant	Gnb5	GRCm38.p3	9:75328044	ATTTTGGAGTAATGT[G/T]TTATGCAGCAATACA	14697
rs8260624	snp	A/G	0.277778	0.248452	intron-variant	Gnb5	Mm_Celera	9:75327992	AGATTAGCTGCATAG[A/G]CTATGCCAGAAGTTG	14697
rs8260625	snp	A/G	0.152778	0.230321	intron-variant	Gnb5	GRCm38.p3	9:75327980	TAGACTATGCCAGAA[A/G]TTGTATATTCTAAAC	14697
rs8260626	in-del	-/G	0.396694	0.202437	intron-variant	Gnb5	GRCm38.p3	9:75327954	TAAACAGAGTTAAAT[-/G]TCTTCTTATTAAACA	14697
rs29639498	snp	A/T	0.444444	0.157135	intron-variant	Gnb5	Mm_Celera	9:75307639	TTTTGCCCACTTTTT[A/T]AAAAATTCATTGAGC	14697
rs29640306	snp	A/G	0.375	0.216506	intron-variant	Gnb5	Mm_Celera	9:75317054	ACCTGAACCACCGAC[A/G]TGTTTGGTTTTTTTA	14697
rs29687657	snp	A/T	0.5	0	intron-variant	Gnb5	Mm_Celera	9:75316842	ACCTTGTTTTTTTTT[A/T]AAATAGGTCTCTCAT	14697
rs29695786	snp	C/T	0.444444	0.157135	intron-variant	Gnb5	Mm_Celera	9:75307500	AGTTTTAGGAATTCT[C/T]GGGTATAGCTAATTG	14697
rs29737091	snp	C/T	0.444444	0.157135	intron-variant	Gnb5	Mm_Celera	9:75337792	TACACCTATATACCA[C/T]GGGGAGACAGAACAG	14697
rs29738216	snp	C/G	0.5	0	intron-variant	Gnb5	Mm_Celera	9:75323193	ATAGATAGATAGATA[C/G]ATAGATAGATAGATA	14697
rs29738846	snp	A/C	0.475309	0.108333	utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant	Myo5c, Gnb5	Mm_Celera	9:75305259	CCCTAGCAACCTGAC[A/C]ACCCTCCAGTCTGAT	14697
rs29782302	snp	A/G	0.48	0.0979796	intron-variant	Gnb5	Mm_Celera	9:75317377	AAGGTTATCCTCCAC[A/G]ACATAATGAGTTTGA	14697
rs29879056	snp	C/T	0.432133	0.171253	intron-variant, downstream-variant-500B	Gnb5, Myo5c	Mm_Celera	9:75306529	TCTCTACAACCTTTG[C/T]GACTTTATCTCAAAA	14697
rs29887775	snp	A/G	0.5	0	intron-variant	Gnb5	Mm_Celera	9:75330556	CTGCCGAGAAGAGAT[A/G]CTGTGACCACAGCAA	14697
rs29892234	snp	A/C	0.5	0	intron-variant	Gnb5	Mm_Celera	9:75325798	ACCATCAGCGCAGTG[A/C]CTGGGCTGTTAGTGT	14697
rs30034372	snp	C/T	0.444444	0.157135	intron-variant	Gnb5	Mm_Celera	9:75330851	GACCAAGCATTCACA[C/T]CCATGAGTCTATGGG	14697
rs30037086	snp	C/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Gnb5, LOC102636700	Mm_Celera	9:75312814	AACATGACTTCTGGG[C/T]CAGCCTGCTCTACAA	14697
rs30038864	snp	A/G	0.444444	0.157135	intron-variant	Gnb5	Mm_Celera	9:75320844	TCACCGGGCAGTGGT[A/G]GCGCACGCCTTTAAT	14697
rs30137837	snp	C/T	0.5	0	intron-variant	Gnb5	Mm_Celera	9:75323049	CACATGGCAGCTCAC[C/T]GGTCTGTAACTCCAG	14697
rs30174053	snp	C/G	0.5	0	intron-variant	Gnb5	Mm_Celera	9:75323189	ATAGATAGATAGATA[C/G]ATAGATAGATAGATA	14697
rs30183085	snp	A/G	0.444444	0.157135	intron-variant	Gnb5	Mm_Celera	9:75330949	CCTTTTCCCTTTAAC[A/G]AAAGAGATTACTCAC	14697
rs30183473	snp	C/T	0.444444	0.157135	intron-variant	Gnb5	Mm_Celera	9:75320850	GGCAGTGGTAGCGCA[C/T]GCCTTTAATCCCAGC	14697
rs30222952	snp	C/G	0.375	0.216506	intron-variant, nc-transcript-variant	Gnb5, LOC102636700	Mm_Celera	9:75310407	TACTGACCTCACCAA[C/G]GGGCCAAGACCTGGG	14697
rs30241458	snp	A/G	0.444444	0.157135	intron-variant	Gnb5, LOC102636700	Mm_Celera	9:75310952	GTTTAGTGGGCAAAG[A/G]CCCCTGCCATCAAGA	14697
rs30262544	snp	A/G	0.444444	0.157135	intron-variant	Gnb5	Mm_Celera	9:75342117	CCCCACACACCATAC[A/G]CATGCACACACACAG	14697
rs30271217	snp	A/T	0.46875	0.121031	utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant	Myo5c, Gnb5	GRCm38.p3	9:75304834	ATCTTTTTTCTGAAA[A/T]TTTTAAAACTTGTTA	14697
rs30424888	snp	C/T	0.5	0	intron-variant	Gnb5	Mm_Celera	9:75317321	GGTAATGCAGGCCTC[C/T]TACGACTCCAGCACT	14697
rs30436781	snp	C/T	0.48	0.0979796	intron-variant	Gnb5	Mm_Celera	9:75319183	GCTGGGGGAGCTTTA[C/T]CCAGACTCTTCGCTC	14697
rs30439314	snp	A/G	0.498615	0.0262793	intron-variant	Gnb5	Mm_Celera	9:75309524	GTTACCTTTTGTGCT[A/G]TAACTCGCTCTTCAT	14697
rs30478992	snp	A/C	0.444444	0.157135	intron-variant	Gnb5	Mm_Celera	9:75330852	ACCAAGCATTCACAC[A/C]CATGAGTCTATGGGG	14697
rs30492405	snp	C/T	0.429688	0.173817	intron-variant	Gnb5	Mm_Celera	9:75320161	TCAAAAAGAACCTGC[C/T]GGCTTCCATGTGCTG	14697
rs32951444	snp	A/C	0.32	0.24	intron-variant	Gnb5	Mm_Celera	9:75309554	TGCAAGCCTAGCAAT[A/C]GACATGATATCTCTG	14697
rs32951446	snp	A/T	0.142012	0.225474	intron-variant	Gnb5	Mm_Celera	9:75309783	TGCAAGTCAACCCTT[A/T]GCCCAACTGCACAGC	14697
rs32951448	snp	C/T	0.32	0.24	intron-variant	Gnb5	Mm_Celera	9:75309807	GCACAGCTTCTAGTT[C/T]CTTCTCTGGCCCTGT	14697
rs32951450	snp	A/G	0.142012	0.225474	intron-variant, downstream-variant-500B	Gnb5, LOC102636700	Mm_Celera	9:75309934	CAGTCCAGCTCAGGG[A/G]TGATTTCCTTGAATC	14697
rs32951452	snp	A/C	0.32	0.24	intron-variant, downstream-variant-500B	Gnb5, LOC102636700	Mm_Celera	9:75309983	GAGCAGCTATGAAAT[A/C]AGCAGGACAGAGCTG	14697
rs32951974	snp	C/T	0.42	0.183303	intron-variant	Gnb5	Mm_Celera	9:75321224	ACTGTTGTATAAAGC[C/T]TTCCACCCATGCCAA	14697
rs32951976	snp	G/T	0.489796	0.070696	intron-variant	Gnb5	Mm_Celera	9:75321332	AAAGAAGGGAGAGAG[G/T]TTCCCACCTGTCTTT	14697
rs32951978	snp	A/C	0.375	0.216506	intron-variant	Gnb5	Mm_Celera	9:75321368	ACCCCTGTTCTTATG[A/C]CTCCTTTAAATTCAG	14697
rs32951980	snp	C/T	0.473373	0.11227	intron-variant	Gnb5	Mm_Celera	9:75321371	CCTGTTCTTATGCCT[C/T]CTTTAAATTCAGGCT	14697
rs32951982	snp	A/G/T	0.277778	0.248452	intron-variant	Gnb5	Mm_Celera	9:75321392	AATTCAGGCTCTCAT[A/G/T]GCCTGCCAGCCAGGA	14697
rs32952274	snp	A/G	0.32	0.24	intron-variant, downstream-variant-500B	Gnb5, LOC102636700	Mm_Celera	9:75310013	GGCTGCTCCCTATTA[A/G]CCTCCCAGTCCTCCA	14697
rs32952276	snp	C/T	0.124444	0.216185	intron-variant, downstream-variant-500B	Gnb5, LOC102636700	Mm_Celera	9:75310207	TGTCCTCTTCCTTCC[C/T]AAGGCTGCTGTTGCT	14697
rs32952278	snp	A/T	0.32	0.24	intron-variant	Gnb5, LOC102636700	Mm_Celera	9:75311158	TCCAAGGATCCGTTG[A/T]AAGCATGATTTGTAA	14697
rs32952280	snp	C/T	0.277778	0.248452	intron-variant	Gnb5, LOC102636700	Mm_Celera	9:75311318	AAGAGAAGGAGGCTC[C/T]GGTCTCCAGAAGCAC	14697
rs32952282	snp	C/T	0.32	0.24	intron-variant	Gnb5, LOC102636700	Mm_Celera	9:75311790	GGGGCTCTCTAAGGG[C/T]CATGTGAAGTCATGG	14697
rs32952283	snp	A/C	0.32	0.24	intron-variant	Gnb5, LOC102636700	Mm_Celera	9:75311870	TTTTTGCATCTGTCT[A/C]CTCCCAGTCTACCTA	14697
rs32952804	snp	C/G	0.46875	0.121031	intron-variant	Gnb5	Mm_Celera	9:75321502	TTGCCCTGTCTGATG[C/G]TTCCAGACTGTGCAC	14697
rs32952806	snp	C/T	0.497041	0.0383476	intron-variant	Gnb5	Mm_Celera	9:75321814	TAGAGACACCGTGGG[C/T]GCAGGTCAGGGAACA	14697
rs32952808	snp	C/T	0.142012	0.225474	intron-variant	Gnb5	Mm_Celera	9:75321940	TGTTCTGCCAAAGAG[C/T]GGAGTCCCCTGACCG	14697
rs32952810	snp	C/T	0.18	0.24	intron-variant	Gnb5	Mm_Celera	9:75322073	CCCGTGGAGAACAAC[C/T]GTTTTAGGTGTACAA	14697
rs32952811	snp	C/G	0.459184	0.136902	intron-variant	Gnb5	Mm_Celera	9:75322291	CTCTGTGCCAGGCTT[C/G]AGTAGCTAGCAAGAA	14697
rs32952812	snp	A/T	0.142012	0.225474	intron-variant	Gnb5	Mm_Celera	9:75322411	GCAGGTGGCTCAAGC[A/T]GAACACACCGCTATC	14697
rs32952985	snp	A/C	0.260355	0.249785	intron-variant, upstream-variant-2KB	Gnb5, LOC102636700	Mm_Celera	9:75312953	ACAGAGACATAGGGA[A/C]TAAAGATGGTTGGTG	14697
rs32952987	snp	A/G	0.165289	0.235211	intron-variant, upstream-variant-2KB	Gnb5, LOC102636700	Mm_Celera	9:75313464	GGAGGAGGCCTAAGT[A/G]GAAACCTATCTGTGA	14697
rs32952988	snp	G/T	0.35503	0.226867	intron-variant, upstream-variant-2KB	Gnb5, LOC102636700	Mm_Celera	9:75313536	TGGAAGTGTGACACC[G/T]AGTGATCATGGCCCT	14697
rs32952990	snp	A/G	0.132653	0.220748	intron-variant, upstream-variant-2KB	Gnb5, LOC102636700	Mm_Celera	9:75313656	ACTGTTGCTGGAGAG[A/G]AGCCGCTGGAGTTAT	14697
rs32952992	snp	G/T	0.486111	0.0821678	intron-variant, utr-variant-5-prime, nc-transcript-variant	Gnb5, LOC102636700	Mm_Celera	9:75314254	TTGCGTTTCTCTCCC[G/T]GCTGCATCCGGACGA	14697
rs32953574	snp	C/T	0.459184	0.136902	synonymous-codon, nc-transcript-variant	Gnb5	Mm_Celera	9:75334190	GGATAATAAGTGCTC[C/T]GTGTATCCACTGACA	14697
rs32953576	snp	C/T	0.244898	0.249948	synonymous-codon, nc-transcript-variant	Gnb5	Mm_Celera	9:75334208	GTATCCACTGACATT[C/T]GACAAGAACGAGAAC	14697
rs32953578	snp	A/G	0.408163	0.193609	intron-variant	Gnb5	Mm_Celera	9:75334480	GTCGAGTTGAGACAA[A/G]CTCTGGCTGTTGGCT	14697
rs32953580	snp	C/T	0.260355	0.249785	intron-variant	Gnb5	Mm_Celera	9:75334576	ATGGCTGCTGAGCTG[C/T]AGGCCTGTGCActgc	14697
rs32953582	snp	C/T	0.336735	0.234472	intron-variant	Gnb5	Mm_Celera	9:75335058	CCACAGCAGGGGCAG[C/T]ACAGCTCCAACACTC	14697
rs32953654	snp	C/T	0.495868	0.0452663	intron-variant	Gnb5	Mm_Celera	9:75323423	AGACATCTCAGTAGC[C/T]TGTGACAGTTGTTCC	14697
rs32953656	snp	G/T	0.375	0.216506	intron-variant	Gnb5	Mm_Celera	9:75323485	CCGTATAGATTTCAT[G/T]TGTGCGTGGCTGCTT	14697
rs32953658	snp	A/C	0.197531	0.244432	intron-variant	Gnb5	Mm_Celera	9:75323648	CACAGCACAGCACCA[A/C]GGGGCACAGCACAGC	14697
rs32953660	snp	C/G	0.493827	0.0552116	intron-variant	Gnb5	Mm_Celera	9:75323758	TTAGTGTTTGACTTG[C/G]AAAGAAAGTTTGAAG	14697
rs32953662	snp	A/G	0.336735	0.234472	intron-variant	Gnb5	Mm_Celera	9:75323807	TAGAGCCAACATTGG[A/G]ACCCCAAGAAAGAAA	14697
rs32953744	snp	A/G	0.165289	0.235211	intron-variant, upstream-variant-2KB	Gnb5, LOC102636700	Mm_Celera	9:75314965	AGGCCTCAGCCTTTT[A/G]AATTCCATTTGGAGA	14697
rs32953746	snp	G/T	0.142012	0.225474	intron-variant, upstream-variant-2KB	Gnb5, LOC102636700	Mm_Celera	9:75315045	CTTGCTGGAAGTACA[G/T]AACCCTGGTTGTGTC	14697
rs32953748	snp	C/T	0.375	0.216506	intron-variant, upstream-variant-2KB	Gnb5, LOC102636700	Mm_Celera	9:75315188	TAACAAGATAAGGTC[C/T]GGTGCAGCTAGATTG	14697
rs32953750	snp	C/T	0.336735	0.234472	intron-variant, upstream-variant-2KB	Gnb5, LOC102636700	Mm_Celera	9:75315458	GTGACACAGGGTCTG[C/T]CTTCTCAGAGCCTTG	14697
rs32953752	snp	A/T	0.42	0.183303	intron-variant, upstream-variant-2KB	Gnb5, LOC102636700	Mm_Celera	9:75315518	CAGGCTTGGTATCCC[A/T]GCCTTGGACTTCTCC	14697
rs32954004	snp	A/G	0.336735	0.234472	intron-variant	Gnb5	Mm_Celera	9:75344108	TTCCATGCCTTCCCC[A/G]GAAGACAATGACTAC	14697
rs32954006	snp	G/T	0.336735	0.234472	utr-variant-3-prime, nc-transcript-variant	Gnb5	Mm_Celera	9:75344979	ATCTTCTGACAGCGT[G/T]CAAGAATGTGTGTCC	14697
rs32954008	snp	A/G	0.231111	0.249285	utr-variant-3-prime, nc-transcript-variant	Gnb5	Mm_Celera	9:75345318	GTACCTTTTCTTGGC[A/G]TGGACTGTGGCTTCT	14697
rs32954010	snp	A/G	0.231111	0.249285	utr-variant-3-prime, nc-transcript-variant	Gnb5	Mm_Celera	9:75345609	AATTCACTTGTGATC[A/G]ATGGCAGTCTAGGCT	14697

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