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
rs3698924	snp	C/T	0.5	0	intron-variant	Myo1f	Mm_Celera	17:33573221	atatatatatatata[C/T]atatatatatatata	17916
rs3699451	snp	A/G	0.455	0.143091	intron-variant	Myo1f	Mm_Celera	17:33573295	ATTGATTGAGAGAAT[A/G]TGTGCATGCTATTGT	17916
rs3708674	snp	C/T	0.5	0	intron-variant	Myo1f	Mm_Celera	17:33576302	ATCCAGCCATCATTT[C/T]ATAAGAGACACAAGG	17916
rs3708676	snp	A/G	0.495868	0.0452663	intron-variant	Myo1f	Mm_Celera	17:33576303	TCCAGCCATCATTTC[A/G]TAAGAGACACAAGGT	17916
rs3709196	snp	C/T	0.5	0	intron-variant	Myo1f	Mm_Celera	17:33576360	AAAGGGTGGTCTTGT[C/T]GGGATAGATTAAGGG	17916
rs3709219	snp	G/T	0.5	0	intron-variant	Myo1f	Mm_Celera	17:33576369	TCTTGTTGGGATAGA[G/T]TAAGGGGTAAGAAGA	17916
rs3724223	snp	C/T	0.415225	0.187619	synonymous-codon	Myo1f	Mm_Celera	17:33576442	TCTCAAGACATACAT[C/T]GGCTCAGTGCTAATC	17916
rs3724852	snp	A/G	0.5	0	intron-variant	Myo1f	Mm_Celera	17:33576546	CAGGGTTGGATGGGT[A/G]GAAGTATCTCCATAC	17916
rs3724871	snp	G/T	0.5	0	intron-variant	Myo1f	Mm_Celera	17:33576550	GTTGGATGGGTGGAA[G/T]TATCTCCATACCTAC	17916
rs6193248	snp	A/G	0.5	0	intron-variant	Myo1f	Mm_Celera	17:33595063	ACGGGGTGAAGGGGA[A/G]GCTTTCGTTACTTTG	17916
rs6193711	snp	A/G	0.48	0.0979796	intron-variant	Myo1f	Mm_Celera	17:33595149	CCCATATGGAAATGA[A/G]GCAAAGTAAGAGCCA	17916
rs6194687	snp	A/G	0.426035	0.177515	intron-variant	Myo1f	Mm_Celera	17:33595294	GATCAGGGAGAGGAC[A/G]AATACAGGGTATAGT	17916
rs6249567	snp	A/G	0.5	0	intron-variant	Myo1f	Mm_Celera	17:33563033	ATCTGGGGTGAATTC[A/G]AAAGCTCCATCATTT	17916
rs6249614	snp	A/C	0.5	0	intron-variant	Myo1f	GRCm38.p3	17:33563059	CATTTGGCTCTTCCT[A/C]TCACTTTGGACCCAT	17916
rs6262247	snp	C/T	0.5	0	intron-variant	Myo1f	Mm_Celera	17:33563165	ATTGTTGAATCTGGG[C/T]AGCTGATTCCATGAG	17916
rs6262663	snp	A/G	0.5	0	intron-variant	Myo1f	Mm_Celera	17:33563197	TCTACTGCACTTGGA[A/G]TTCTTATATTTTCAN	17916
rs6262681	snp	A/G	0.5	0	intron-variant	Myo1f	Mm_Celera	17:33563212	NTTCTTATATTTTCA[A/G]TGAAGAAACTGAGGC	17916
rs6314367	snp	A/T	0.5	0	intron-variant	Myo1f	Mm_Celera	17:33575392	CATcttcccactttc[A/T]ttaaggtgatcaaga	17916
rs6314402	snp	C/T	0.5	0	intron-variant	Myo1f	Mm_Celera	17:33575416	atcaagacagtttcc[C/T]ccagacatgcaacag	17916
rs6327335	snp	A/G	0.5	0	intron-variant	Myo1f	Mm_Celera	17:33575450	aaactgacctagaga[A/G]tccatcactgagact	17916
rs6327467	snp	A/G	0.5	0	intron-variant	Myo1f	Mm_Celera	17:33575536	acagtggtggcgcac[A/G]cctttaaccccagca	17916
rs6327911	snp	C/T	0.5	0	intron-variant	Myo1f	Mm_Celera	17:33575585	gtggatctctgaatt[C/T]gaggccagattggtc	17916
rs6329696	snp	C/T	0.473373	0.11227	synonymous-codon	Myo1f	Mm_Celera	17:33575928	GGATGACTACATTTT[C/T]GTATCCCAAGTAGCG	17916
rs6330129	snp	A/T	0.473373	0.11227	intron-variant	Myo1f	Mm_Celera	17:33575951	AAGTAGCGCAGGGGC[A/T]CAGGAGGATGAAGTA	17916
rs29498269	snp	A/G	0.375	0.216506	intron-variant	Myo1f	Mm_Celera	17:33607239	CTAAGATAGCTACAG[A/G]CTAGACATTCAGGCT	17916
rs29500136	snp	A/G	0.32	0.24	intron-variant	Myo1f	Mm_Celera	17:33562001	ATGAACAATCAAAGG[A/G]CCCACAACTGATTGG	17916
rs29500737	snp	C/T	0.260355	0.249785	intron-variant	Myo1f	GRCm38.p3	17:33592240	ACACAGAGTTTGAAC[C/T]CGAATGTTTCATATC	17916
rs29501654	snp	C/T	0.444444	0.157135	intron-variant	Myo1f	GRCm38.p3	17:33559819	TTATTTATTTATTTA[C/T]TTACTTACTTACTTA	17916
rs29507176	snp	A/G	0.444444	0.157135	intron-variant	Myo1f	Mm_Celera	17:33584528	TCTAGAACATCCAGG[A/G]CAACATAGAGAGACC	17916
rs29518670	snp	A/T	0.375	0.216506	intron-variant	Myo1f	GRCm38.p3	17:33607033	GAGCTGGACTAACAG[A/T]CGTGCCATCTACCAC	17916
rs29518996	snp	A/G	0.375	0.216506	intron-variant	Myo1f	GRCm38.p3	17:33606855	CTTGTTGAAGATAGT[A/G]TCTCTTGTTGCTTGC	17916
rs29519668	snp	G/T	0.5	0	intron-variant	Myo1f	Mm_Celera	17:33564159	TTTCATTTTATGTGT[G/T]TTTTGTCTGCATATC	17916
rs29522100	snp	C/T	0.444444	0.157135	intron-variant	Myo1f	Mm_Celera	17:33558862	GGGCCTCATCATTGC[C/T]AGGCAAGCACTCCAC	17916
rs29523700	snp	C/T	0.375	0.216506	intron-variant	Myo1f	GRCm38.p3	17:33590503	GCCTTGAACTCACTA[C/T]GTAGCTGAAGATGAA	17916
rs29532529	snp	A/C	0.5	0	intron-variant	Myo1f	Mm_Celera	17:33582671	TGCATTTGAGAGCTA[A/C]GATGGTTGTCAAGGA	17916
rs29537187	snp	A/G	0.5	0	intron-variant	Myo1f	Mm_Celera	17:33571329	ATACAGGGAATCCCT[A/G]TCTCGAAAAACCAAA	17916
rs33065090	snp	A/T	0.5	0	intron-variant	Myo1f	Mm_Celera	17:33571738	AAACTCTGCTTCCCC[A/T]ACGTGCCACTAGGGA	17916
rs33072396	snp	C/G	0.444444	0.157135	intron-variant	Myo1f	Mm_Celera	17:33577342	AACGTATGCATGTAG[C/G]AGTTCAAAGACAATT	17916
rs33072821	snp	G/T	0.48	0.0979796	intron-variant	Myo1f	Mm_Celera	17:33572259	CTCTAACCCTCTAGA[G/T]CTGTAAGTGGAATTT	17916
rs33083115	snp	C/T	0.5	0	intron-variant	Myo1f	Mm_Celera	17:33605596	AGCTGGGCATGGTGG[C/T]GCACCCCTTTAATCC	17916
rs33093944	snp	A/C	0.444444	0.157135	intron-variant	Myo1f	GRCm38.p3	17:33577394	CCCACCATCTCAAGA[A/C]TTGAACTCATGTCTT	17916
rs33120674	snp	C/T	0.375	0.216506	intron-variant	Myo1f	GRCm38.p3	17:33590418	TCAAGGCCAGCTTGA[C/T]CTATACAGTTTGTTT	17916
rs33121736	snp	C/T	0.375	0.216506	utr-variant-3-prime	Myo1f	GRCm38.p3	17:33607586	AGTCTCCATTTTCTC[C/T]TGTGTCCAATAGTAG	17916
rs33127424	snp	C/T	0.444444	0.157135	intron-variant	Myo1f	GRCm38.p3	17:33559807	TTATTTATTTATTTA[C/T]TTATTTATTTATTTA	17916
rs33129115	snp	A/G	0.444444	0.157135	intron-variant	Myo1f	GRCm38.p3	17:33583621	TAAAATATAACAAGA[A/G]GGTGGTGACCAGTGG	17916
rs33133832	snp	A/G	0.32	0.24	intron-variant	Myo1f	GRCm38.p3	17:33601012	GGCTGCCCATCCCCT[A/G]GGGACCACCCATCAG	17916
rs33139073	snp	A/T	0.290657	0.246672	intron-variant	Myo1f	GRCm38.p3	17:33562131	TCTGTGTGGAGAATT[A/T]AAGGAGGTATAAGAG	17916
rs33142612	snp	C/G	0.375	0.216506	intron-variant	Myo1f	Mm_Celera	17:33587117	TAATGAGATTTGACA[C/G]CTTCTTCTGGTGTGA	17916
rs33156121	snp	C/T	0.5	0	intron-variant	Myo1f	Mm_Celera	17:33564391	TCATGTAGGCTAGTG[C/T]CCAATTGAGTGCATT	17916
rs33159589	snp	C/T	0.444444	0.157135	intron-variant	Myo1f	GRCm38.p3	17:33602499	GGGCCACAATTCAAA[C/T]CTATATCTGATTTCT	17916
rs33159952	snp	A/C	0.497778	0.0332592	intron-variant	Myo1f	Mm_Celera	17:33571839	CCCTGAGCACATAGT[A/C]ACCCCTTTGCACACA	17916
rs33170972	snp	C/T	0.391111	0.206368	intron-variant	Myo1f	Mm_Celera	17:33601632	CTTCCTACACCCTCA[C/T]TTCATGCTCTCTTAC	17916
rs33173179	snp	A/G	0.304688	0.243945	upstream-variant-2KB	Myo1f	GRCm38.p3	17:33555621	GGGTAAGCTCCAAAC[A/G]GTTCCCTCAGCCCTG	17916
rs33177400	snp	G/T	0.444444	0.157135	intron-variant	Myo1f	Mm_Celera	17:33572985	TGCCATCACTTGACA[G/T]AAAGGCAGAAAGTTG	17916
rs33191589	snp	A/T	0.54	0.18	intron-variant	Myo1f	GRCm38.p3	17:33560304	AATCTAGAGAAATGG[A/T]TCAGTGGTTAAAAGT	17916
rs33200665	snp	A/G	0.32	0.24	intron-variant	Myo1f	GRCm38.p3	17:33590247	GAAGATGGAACCCAG[A/G]GCTGTGTTCATGCAA	17916
rs33201592	snp	C/G	0.375	0.216506	intron-variant	Myo1f	GRCm38.p3	17:33590602	TTTACACATGTTTCT[C/G]TTTAGTTTAACTCTG	17916
rs33203191	snp	C/T	0.444444	0.157135	intron-variant	Myo1f	GRCm38.p3	17:33606720	GCACTTATCTATGTG[C/T]GTATCTGTGTGTATG	17916
rs33216405	snp	C/G	0.444444	0.157135	intron-variant	Myo1f	Mm_Celera	17:33585034	ATTAGAAGAGCACAG[C/G]CTAGGGATGTAGCTC	17916
rs33220696	snp	A/C/T	0.48	0.0979796	intron-variant	Myo1f	GRCm38.p3	17:33573609	ACGAGTTCTTGCCTG[A/C/T]GTGCCCAAAGTCTTT	17916
rs33221034	snp	A/G	0.5	0	intron-variant	Myo1f	Mm_Celera	17:33571114	TGGTGGTGGGTTTTG[A/G]GTTTTGTTTTACATT	17916
rs33223468	snp	A/T	0.444444	0.157135	intron-variant	Myo1f	GRCm38.p3	17:33602714	ATAGCTCTCTTATAT[A/T]CTACAAGATGCAGGA	17916
rs33232592	snp	C/T	0.444444	0.157135	intron-variant	Myo1f	GRCm38.p3	17:33559815	TTATTTATTTATTTA[C/T]TTATTTACTTACTTA	17916
rs33239067	snp	A/G/T	0.444444	0.157135	intron-variant	Myo1f	GRCm38.p3	17:33579405	TTCTGAAATGTGCTG[A/G/T]GGGGGCGGAGAAACG	17916
rs33242646	snp	A/T	0.375	0.216506	synonymous-codon	Myo1f	GRCm38.p3	17:33607303	TTCTCCCACAGACTC[A/T]TCTGGCTGGTGGAAG	17916
rs33249673	snp	C/T	0.5	0	intron-variant	Myo1f	Mm_Celera	17:33564306	GGTCTTTTGCAAGAA[C/T]AGTCAGTGCTCTTAA	17916
rs33252495	snp	A/G	0.375	0.216506	intron-variant	Myo1f	GRCm38.p3	17:33607261	ATTCAGGCTTTCTCC[A/G]GTGTACACTGGGCAC	17916
rs33261282	snp	C/T	0.444444	0.157135	intron-variant	Myo1f	GRCm38.p3	17:33592346	TGACCACCTCATCTC[C/T]GTCTCTGTCTCTGTC	17916
rs33269760	snp	A/G	0.426035	0.177515	intron-variant	Myo1f	Mm_Celera	17:33593454	AATAATCAAAACACA[A/G]TTTCTCAAACCTAAA	17916
rs33297755	snp	C/T	0.32	0.24	intron-variant	Myo1f	GRCm38.p3	17:33601007	GGCCAGGCTGCCCAT[C/T]CCCTGGGGACCACCC	17916
rs33313056	snp	C/G	0.5	0	intron-variant	Myo1f	GRCm38.p3	17:33604522	AGTATCTAGGGCTGT[C/G]CTGAGACCCATGCTG	17916
rs33313861	snp	C/T	0.444444	0.157135	intron-variant	Myo1f	Mm_Celera	17:33605883	CACCTAGTGCCTAAG[C/T]ATCTCTATTATTTTA	17916
rs33317270	snp	A/G	0.375	0.216506	intron-variant	Myo1f	GRCm38.p3	17:33562350	AACAACCCCCTGGCT[A/G]GTAGAATATAGGTCC	17916
rs33318476	snp	G/T	0.5	0	intron-variant	Myo1f	Mm_Celera	17:33571785	AGAACACCTGAAGGT[G/T]TTAATCCCTATTTAC	17916
rs33323321	snp	A/G	0.444444	0.157135	intron-variant	Myo1f	Mm_Celera	17:33573084	ATTTGAAGGAAGGAA[A/G]GAAGGAAGGAAGGAA	17916
rs33334959	snp	A/G	0.5	0	intron-variant	Myo1f	Mm_Celera	17:33558428	GGTTCTTATGGGTAG[A/G]TTGGAGGTGATGATA	17916
rs33359638	snp	C/T	0.444444	0.157135	intron-variant	Myo1f	GRCm38.p3	17:33559811	TTATTTATTTATTTA[C/T]TTATTTATTTACTTA	17916
rs33367243	snp	C/G/T	0.375	0.216506	intron-variant	Myo1f	GRCm38.p3	17:33590428	CTTGACCTATACAGT[C/G/T]TGTTTCAGGTCAGCC	17916
rs33371743	snp	G/T	0.444444	0.157135	intron-variant	Myo1f	GRCm38.p3	17:33605852	ATCCTAAAGCACAAG[G/T]GCTGTGACTTCATCA	17916
rs33391932	snp	A/G	0.375	0.216506	intron-variant	Myo1f	GRCm38.p3	17:33606354	ATGGAAGGGTGGGAA[A/G]GAGATGGAAGTCTGG	17916
rs33397801	snp	A/G	0.444444	0.157135	intron-variant	Myo1f	GRCm38.p3	17:33579837	TTCCTGGGAGTCAGG[A/G]ATATGCTAACGTGGT	17916
rs33407547	snp	A/T	0.375	0.216506	intron-variant	Myo1f	Mm_Celera	17:33587179	TAATTAAATAAATTT[A/T]AAAAAATAGCAACCC	17916
rs33418822	snp	A/T	0.375	0.216506	intron-variant	Myo1f	GRCm38.p3	17:33589850	AGATACTTTTCTTTC[A/T]TTTTTCTTTTTTTTT	17916
rs33423111	snp	A/G	0.375	0.216506	intron-variant	Myo1f	GRCm38.p3	17:33606500	ATACTTATAATCCTA[A/G]AACTTCAGGAGGATG	17916
rs33426352	snp	A/G	0.489796	0.070696	intron-variant	Myo1f	Mm_Celera	17:33572875	AGAGAATAGGAGACA[A/G]GAAAGGAGCTGGTAA	17916
rs33434735	snp	C/T	0.5	0	intron-variant	Myo1f	Mm_Celera	17:33583117	GTTCTGTCAACAGAA[C/T]CCATATTTTAATTTT	17916
rs33439284	snp	A/G	0.5	0	intron-variant	Myo1f	Mm_Celera	17:33564450	CCCACTGAATACTGA[A/G]ATTCAAGATGTATAC	17916
rs33447194	snp	A/T	0.375	0.216506	intron-variant	Myo1f	GRCm38.p3	17:33606380	TCTGGGTACAGGCTT[A/T]GTCAGTAAACTACTC	17916
rs33453312	snp	A/G	0.48	0.0979796	intron-variant	Myo1f	Mm_Celera	17:33572256	GGACTCTAACCCTCT[A/G]GAGCTGTAAGTGGAA	17916
rs33466030	snp	C/T	0.444444	0.157135	intron-variant	Myo1f	Mm_Celera	17:33602913	GCTATAGTGTACTAG[C/T]ATAAATAAAATAAAA	17916
rs33477985	snp	A/G	0.375	0.216506	utr-variant-3-prime	Myo1f	GRCm38.p3	17:33607695	ACTGCCCAGAGTTAG[A/G]AGACGTGGACAGTTA	17916
rs33480619	snp	A/C	0.459184	0.136902	intron-variant	Myo1f	GRCm38.p3	17:33601022	CCCCTGGGGACCACC[A/C]ATCAGCTTCTGGCTT	17916
rs33491802	snp	C/T	0.375	0.216506	intron-variant	Myo1f	GRCm38.p3	17:33606555	AGTCTCCAATTAAAA[C/T]AGGACTGAGTGTGAC	17916
rs33500532	snp	C/T	0.444444	0.157135	synonymous-codon	Myo1f	GRCm38.p3	17:33602581	GTCAGCGCAGGCTCC[C/T]ACTCGAGCAGCCCCT	17916
rs33502337	snp	C/T	0.444444	0.157135	intron-variant	Myo1f	GRCm38.p3	17:33583679	CCCATTTTTACCCTC[C/T]CATAGGCCATCAACC	17916
rs33505312	snp	C/T	0.456747	0.140554	upstream-variant-2KB	Myo1f	GRCm38.p3	17:33555480	CTGAAGAGAACTAAG[C/T]GGCCAGTCCTGCAGT	17916
rs33539395	snp	C/G	0.444444	0.157135	intron-variant	Myo1f	GRCm38.p3	17:33558549	TGGAAGCCAGACAAG[C/G]ATATCACATCCCCTT	17916
rs33540027	snp	A/C	0.492188	0.0620098	upstream-variant-2KB	Myo1f	GRCm38.p3	17:33555411	GACCATAAAGGGTTT[A/C]CATGGGAACTCTGAG	17916
rs33551112	snp	A/T	0.375	0.216506	intron-variant	Myo1f	GRCm38.p3	17:33590539	ACTTCTGATTCTCCT[A/T]CCTCCATACCCTGAG	17916
rs33589121	snp	C/T	0.391111	0.206368	intron-variant	Myo1f	Mm_Celera	17:33556447	AGCACTGAAAATAAG[C/T]CATCATCATCCTCAT	17916

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