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
rs3089222	snp	C/T	0.21875	0.248039	intron-variant	Myo1e	Mm_Celera	9:70287509	CAAACCTCACGGAAA[C/T]GTGTGTTGACTTCAT	71602
rs3660196	snp	C/T	0.444444	0.157135	intron-variant	Myo1e, LOC105243448	Mm_Celera	9:70212887	CCAACTGCTGAGCCA[C/T]CTTCCTAGCCCCATT	71602
rs3692467	snp	A/G	0.5	0	intron-variant	Myo1e	Mm_Celera	9:70253879	CAACAGCCATTCTCA[A/G]CCGCTATGGGGAGCC	71602
rs3692483	snp	C/T	0.5	0	intron-variant	Myo1e	Mm_Celera	9:70253881	ACAGCCATTCTCAGC[C/T]GCTATGGGGAGCCTG	71602
rs3701883	snp	C/T	0.5	0	intron-variant	Myo1e, LOC105243448	Mm_Celera	9:70240502	AGGCTAGACAAATGG[C/T]TCAGCAGTCGAGAGC	71602
rs3702005	snp	A/G	0.5	0	intron-variant	Myo1e	Mm_Celera	9:70312817	AGGCCCAGGGCTGGG[A/G]TTACAGGAACGCACC	71602
rs3702021	snp	A/C	0.5	0	intron-variant	Myo1e	Mm_Celera	9:70312825	GGCTGGGATTACAGG[A/C]ACGCACCAACATTCC	71602
rs3702515	snp	A/G	0.444444	0.157135	intron-variant	Myo1e	Mm_Celera	9:70312893	GAAGTCAAGCAAAAC[A/G]ATGGAATTAGGCAAG	71602
rs3702576	snp	A/G	0.489796	0.070696	intron-variant	Myo1e	Mm_Celera	9:70312940	GGCAAAGCCTATTGC[A/G]ATGGCTGCTGTGAGC	71602
rs3703045	snp	A/C/T	0.489796	0.070696	intron-variant	Myo1e	GRCm38.p3	9:70312970	CTGCAGAGTGAGCAG[A/C/T]GATGGAGGTAGTGTG	71602
rs3712560	snp	A/G	0.5	0	intron-variant	Myo1e, LOC105243448	Mm_Celera	9:70211726	CGCGCATGCAGTCTA[A/G]AGCCTGTGCTGGACT	71602
rs3713181	snp	C/T	0.5	0	intron-variant	Myo1e, LOC105243448	Mm_Celera	9:70211805	CTGTGGCTCATCTGC[C/T]CGGAGCCACTATGAG	71602
rs3713899	snp	A/G	0.5	0	intron-variant	Myo1e, LOC105243448	Mm_Celera	9:70211921	ATGTCAGTGTTCATT[A/G]CTACATCTACGTCTT	71602
rs3713914	snp	C/T	0.5	0	intron-variant	Myo1e, LOC105243448	Mm_Celera	9:70211931	TCATTGCTACATCTA[C/T]GTCTTCTCCTACGGC	71602
rs3713982	snp	A/G	0.304688	0.243945	intron-variant	Myo1e, LOC105243448	Mm_Celera	9:70211969	GGGAAGGCGGTTGCC[A/G]GGTATTTTGTACCTG	71602
rs6212611	snp	A/G	0.5	0	intron-variant	Myo1e	Mm_Celera	9:70320305	CTCCTCCCTGGAGTT[A/G]CTTCAGTAAGGAAAC	71602
rs6213070	snp	A/G	0.5	0	intron-variant	Myo1e	Mm_Celera	9:70320388	TGGAGGACAGAAGGG[A/G]GAAGATTAGGGCAAG	71602
rs6231851	snp	G/T	0.444444	0.157135	intron-variant	Myo1e, LOC105243448	Mm_Celera	9:70215845	ACATGAAGATTGGGG[G/T]AGGAGGTTGGGGAGC	71602
rs6242578	snp	A/G	0.5	0	intron-variant	Myo1e	Mm_Celera	9:70255876	TCCCTCCCTCTGTAG[A/G]GTTGTCTATGTTGTT	71602
rs6242608	snp	A/G	0.5	0	intron-variant	Myo1e	Mm_Celera	9:70255896	TCTATGTTGTTTTGG[A/G]TGAGTGACACCACGA	71602
rs6242662	snp	G/T	0.5	0	intron-variant	Myo1e	Mm_Celera	9:70255930	ACAGATGACCCTTCT[G/T]TCTGTTGTATATGNC	71602
rs6242681	snp	A/G	0.5	0	intron-variant	Myo1e	Mm_Celera	9:70255944	TNTCTGTTGTATATG[A/G]CAAGGAAATGCTTTG	71602
rs6253097	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	Myo1e, LOC105243448	Mm_Celera	9:70244302	CAGCCCAGATCTCAT[A/G]ATTCTTGAATTGAAA	71602
rs6336847	snp	C/G/T	0.5	0	intron-variant	Myo1e, LOC105243448	GRCm38.p3	9:70228078	ATAGGATTACAAATA[C/G/T]TCAGATCATCTCGGA	71602
rs6337469	snp	A/T	0.5	0	intron-variant	Myo1e, LOC105243448	Mm_Celera	9:70228181	CTCTTCTGACTTTAC[A/T]ACCTGGCCCCCAGAA	71602
rs6338482	snp	C/T	0.5	0	intron-variant	Myo1e	Mm_Celera	9:70255531	aggcaaccagtcatg[C/T]ttcatccaatagagg	71602
rs6338887	snp	A/G	0.5	0	intron-variant	Myo1e	Mm_Celera	9:70255552	ccaatagagggaggt[A/G]gangctctgctaggc	71602
rs6338889	snp	C/T	0.5	0	intron-variant	Myo1e	Mm_Celera	9:70255555	atagagggaggtnga[C/T]gctctgctaggctca	71602
rs6339009	snp	C/T	0.5	0	intron-variant	Myo1e, LOC105243448	Mm_Celera	9:70228402	ACCCTCTCTGCTCCA[C/T]GGGCCCCGGCACACA	71602
rs6339049	snp	A/G	0.5	0	intron-variant	Myo1e, LOC105243448	Mm_Celera	9:70228425	GGCACACAATTTCCC[A/G]TTGGTTGGTTTGGCA	71602
rs6339949	snp	A/G	0.359862	0.224567	intron-variant	Myo1e, LOC105243448	Mm_Celera	9:70221990	ACTGGGAAGTGGTCC[A/G]TGCCACTGTGGAAGC	71602
rs6340059	snp	A/C	0.5	0	intron-variant	Myo1e, LOC105243448	Mm_Celera	9:70222057	GAGGAATATTCTGAA[A/C]GGCTCATAGGGCGGA	71602
rs6341072	snp	C/T	0.5	0	intron-variant	Myo1e, LOC105243448	Mm_Celera	9:70222227	GCTTGTTTTGGTTTT[C/T]TTCATCACTTCAGAA	71602
rs6341135	snp	C/T	0.359862	0.224567	intron-variant	Myo1e, LOC105243448	Mm_Celera	9:70222287	TCAGCTGAACCGAGC[C/T]ATTCTGTTTCCTCCA	71602
rs6398008	snp	A/G	0.5	0	intron-variant	Myo1e	Mm_Celera	9:70277243	acctgctaagtagct[A/G]aggatgaccttgaac	71602
rs6399153	snp	C/G/T	0.5	0	intron-variant	Myo1e	GRCm38.p3	9:70277420	acagacagacagaca[C/G/T]tcaatcaactgagcc	71602
rs6399189	snp	A/G	0.48	0.0979796	intron-variant	Myo1e	Mm_Celera	9:70277438	AATCAACTGAGCCCC[A/G]GCCCAGAGAGACTTT	71602
rs6400160	snp	C/T	0.5	0	intron-variant	Myo1e	GRCm38.p3	9:70277583	GGTTTGTTTCTGTTT[C/T]AGTCAGTGGCNTGAA	71602
rs6400176	snp	A/G	0.5	0	intron-variant	Myo1e	Mm_Celera	9:70277594	GTTTNAGTCAGTGGC[A/G]TGAACAGGAGCCNCG	71602
rs6400190	snp	A/G/T	0.21875	0.248039	intron-variant	Myo1e	Mm_Celera	9:70277607	GCNTGAACAGGAGCC[A/G/T]CGGGAGCTGGTCTTC	71602
rs6403125	snp	C/T	0.5	0	intron-variant	Myo1e	Mm_Celera	9:70316524	TGCAATTTGTTCATT[C/T]GGAGACAGTGGATGA	71602
rs13472135	snp	C/T	0.48	0.0979796	utr-variant-3-prime	Myo1e	Mm_Celera	9:70399680	CAGTCCCTCAGACCC[C/T]CTTACCCTCTCCCTG	71602
rs13472136	snp	C/T	0.375	0.216506	utr-variant-3-prime	Myo1e	Mm_Celera	9:70399263	CCACCCTCTGGAGGC[C/T]GGACTTGGGGCGAAC	71602
rs13472137	snp	G/T			utr-variant-3-prime	Myo1e	Mm_Celera	9:70399162	GTGACTCGATGACAA[G/T]TGCCTTTAGTTGAAG	71602
rs13480263	snp	A/G	0.281951	0.24795	synonymous-codon	Myo1e	Mm_Celera	9:70322427	GTTCAGTCCAGGTGG[A/G]GAACCAGATGGTGGC	71602
rs29588541	snp	C/T	0.5	0	intron-variant	Myo1e	Mm_Celera	9:70253779	GTTGTCTCTCTGAAC[C/T]AAGCACAAGATGAAG	71602
rs29589584	snp	C/G	0.5	0	intron-variant	Myo1e	Mm_Celera	9:70329148	GGGTGCCTGTTTGTG[C/G]CTTTGCCAGCAGCTG	71602
rs29591830	snp	G/T	0.444444	0.157135	intron-variant	Myo1e	Mm_Celera	9:70315497	TGGCAACACCAAGGC[G/T]GCCCACAGAGAGATG	71602
rs29592111	snp	C/G	0.444444	0.157135	intron-variant	Myo1e	Mm_Celera	9:70360607	GTGTGATGGGACTGT[C/G]TTTAAGTGGTTTCAC	71602
rs29592813	snp	C/T	0.444444	0.157135	intron-variant	Myo1e	Mm_Celera	9:70334797	GTCCTTCTTGGAGCA[C/T]TGATTTGAGTGACTG	71602
rs29593032	snp	C/T	0.444444	0.157135	intron-variant, nc-transcript-variant	Myo1e, LOC105243448	Mm_Celera	9:70243337	CCCTGTGGCCCTGAG[C/T]GACACTGGTCGTAGA	71602
rs29593180	snp	C/T	0.375	0.216506	intron-variant	Myo1e	Mm_Celera	9:70249993	ATGACATCTTCCTTA[C/T]GAAGCACAAAGTTTT	71602
rs29593364	snp	A/T	0.32	0.24	intron-variant, nc-transcript-variant	Myo1e, LOC105245017	Mm_Celera	9:70290862	ACTCTCAAGCCTTTT[A/T]AAATTCAGACAGCAA	71602
rs29594783	snp	A/G	0.444444	0.157135	intron-variant	Myo1e	Mm_Celera	9:70333069	GATAACCATTGGGGG[A/G]AAAATCAAAGCCTGA	71602
rs29595609	snp	A/G	0.46875	0.121031	intron-variant	Myo1e	Mm_Celera	9:70377819	TCTCATCTTCCAACC[A/G]TCTTGTGTCTGACAT	71602
rs29596080	snp	A/C/G	0.444444	0.157135	intron-variant	Myo1e	GRCm38.p3	9:70334548	TTTTCCTCATTTTCT[A/C/G]TGTGTTATAAGCCCT	71602
rs29597484	snp	C/T	0.375	0.216506	intron-variant	Myo1e	Mm_Celera	9:70359169	CTCCCTGCAGCTTGG[C/T]AGTAGCCACTGTAGT	71602
rs29604785	snp	A/G	0.375	0.216506	intron-variant	Myo1e, LOC105243448	Mm_Celera	9:70236765	AGTAAATTAATTAAT[A/G]TTCAAATTAAGAAAA	71602
rs29637132	snp	C/G	0.375	0.216506	intron-variant	Myo1e	Mm_Celera	9:70268256	CTCCTAGGCATATGG[C/G]GGAAAAAGCATCTTT	71602
rs29637954	snp	C/T	0.444444	0.157135	intron-variant	Myo1e	Mm_Celera	9:70308939	TCTACTTCCCCAGCC[C/T]TCGGATTGCAGGCAC	71602
rs29638561	snp	A/G	0.375	0.216506	intron-variant	Myo1e, LOC105243448	Mm_Celera	9:70239348	CCAATCAGAAATGCT[A/G]TCTGTCTGTCCACTT	71602
rs29639184	snp	A/G	0.48	0.0979796	intron-variant	Myo1e	Mm_Celera	9:70359760	ACCTATCCATTCATC[A/G]GTTGATAAATATTGT	71602
rs29639212	snp	C/T	0.375	0.216506	intron-variant	Myo1e	Mm_Celera	9:70253331	CAGCAGAGCTCTTCT[C/T]CCTCCTCTGAACTCT	71602
rs29640376	snp	A/T	0.5	0	intron-variant	Myo1e	Mm_Celera	9:70248919	AGGGTTTCCTCATCC[A/T]GGGTTTCACAAGAGT	71602
rs29640670	snp	C/T	0.444444	0.157135	intron-variant	Myo1e	Mm_Celera	9:70331434	CTCTTTTATCTAAGT[C/T]CTGGTGGTGTGATTT	71602
rs29641886	snp	A/G	0.375	0.216506	intron-variant	Myo1e	Mm_Celera	9:70330350	GTGGGGTAGGGTGGG[A/G]TAGTCTCTAGATGGT	71602
rs29643270	snp	A/G	0.375	0.216506	intron-variant	Myo1e	Mm_Celera	9:70288911	ACCGTGGAGCAGATC[A/G]TCCCCTAGGGTGGGA	71602
rs29644208	snp	A/G	0.444444	0.157135	intron-variant	Myo1e, LOC105243448	Mm_Celera	9:70231284	AATCCACATGCTTCT[A/G]CTTCCCAAGTGCTGG	71602
rs29644369	snp	C/T	0.444444	0.157135	intron-variant	Myo1e, LOC105243448	Mm_Celera	9:70231935	TTAGAGGCCCAGGCA[C/T]GGTGAAACATATCTA	71602
rs29644570	snp	C/G	0.401235	0.199068	intron-variant, nc-transcript-variant	Myo1e, LOC105243448	Mm_Celera	9:70243504	GACTCCGGTCAGTAA[C/G]CCATGCCCAGTGTCC	71602
rs29645944	snp	C/T	0.375	0.216506	intron-variant	Myo1e, LOC105243448	Mm_Celera	9:70215165	CATAATTATTTTATG[C/T]CTTTGGGTTTCCTTC	71602
rs29647063	snp	C/T	0.375	0.216506	intron-variant	Myo1e	Mm_Celera	9:70389408	CAGATGGTTGTGAGC[C/T]ACCATGTGGTTGCTG	71602
rs29647825	snp	C/T	0.33241	0.236027	intron-variant	Myo1e, LOC105243448	Mm_Celera	9:70237267	CTGCACCTCGGATGT[C/T]ACCAGCTATCACCAA	71602
rs29648704	snp	C/T	0.444444	0.157135	intron-variant	Myo1e	Mm_Celera	9:70315500	CAACACCAAGGCTGC[C/T]CACAGAGAGATGAGA	71602
rs29648757	snp	C/T	0.48	0.0979796	intron-variant	Myo1e, LOC105243448	Mm_Celera	9:70228210	AATGAGAGGCAGGAA[C/T]TGCCGATATACTTAC	71602
rs29649897	snp	A/G	0.375	0.216506	intron-variant	Myo1e	Mm_Celera	9:70287775	CCCAGAATGCCTGGG[A/G]AAGTTTTCTCACTAG	71602
rs29651214	snp	C/T	0.444444	0.157135	intron-variant	Myo1e	Mm_Celera	9:70355293	CTCTCCCACTTTCCT[C/T]ACCTCTTTCCAATAA	71602
rs29683966	snp	A/G	0.375	0.216506	intron-variant	Myo1e, LOC105243448	Mm_Celera	9:70239663	ATTATTATTTGTATT[A/G]TTATTACTATTATTA	71602
rs29688505	snp	A/T	0.375	0.216506	intron-variant	Myo1e, LOC105243448	Mm_Celera	9:70217560	ACACTCGAAGACATG[A/T]CGTGTATAGGATTAT	71602
rs29690184	snp	A/G	0.375	0.216506	intron-variant	Myo1e, LOC105243448	Mm_Celera	9:70241733	GCCCTCCACTTGGAT[A/G]GAACACTGACGTGCT	71602
rs29690206	snp	G/T	0.48	0.0979796	intron-variant	Myo1e	Mm_Celera	9:70325397	AAGATGGCTGGGCAG[G/T]AAGAGTGCTTGCAGT	71602
rs29691063	snp	G/T	0.375	0.216506	intron-variant	Myo1e	Mm_Celera	9:70301534	TCGATTCCCCAGGGC[G/T]TATCAGGCCATAACC	71602
rs29691088	snp	A/G	0.375	0.216506	intron-variant	Myo1e	Mm_Celera	9:70323907	CCTATATTCACAAAG[A/G]GTGCTCGCCTAACAT	71602
rs29691162	snp	C/G	0.5	0	intron-variant	Myo1e	Mm_Celera	9:70386302	GTGGTGCACATGCAG[C/G]AGAGGACAACTTTCT	71602
rs29691890	snp	G/T	0.375	0.216506	intron-variant	Myo1e	Mm_Celera	9:70357642	TACTGTATACACACA[G/T]TGCCCATACATACAA	71602
rs29693377	snp	A/T	0.48	0.0979796	intron-variant, upstream-variant-2KB	Myo1e	Mm_Celera	9:70258892	GTCTGGAGATAGAGC[A/T]TGGGTCGATAGGATT	71602
rs29694608	snp	C/T	0.277778	0.248452	intron-variant	Myo1e	Mm_Celera	9:70309825	TTCCTGTTTATTGGG[C/T]TGATCAAGGTGAGCC	71602
rs29695959	snp	A/G	0.48	0.0979796	intron-variant	Myo1e	Mm_Celera	9:70390548	CTCAGCCTGCAACCC[A/G]GATGTGCTGTGCATG	71602
rs29701888	snp	A/C	0.375	0.216506	intron-variant	Myo1e	Mm_Celera	9:70322756	TAATCGAACCAGCCC[A/C]GAAAGGTTTCTCTGT	71602
rs29704185	snp	A/T	0.5	0	intron-variant	Myo1e	Mm_Celera	9:70315398	CTGAGGTTCATAGAA[A/T]GTTAAGATGTGGGCC	71602
rs29734441	snp	C/T	0.444444	0.157135	intron-variant	Myo1e	Mm_Celera	9:70331857	ACGATTAATCCTTGC[C/T]TCTTGCCTTTCCTTC	71602
rs29737490	snp	G/T	0.375	0.216506	intron-variant	Myo1e	Mm_Celera	9:70394274	CTGTGCAGGCATGGT[G/T]AAGGCACACAGCCTT	71602
rs29737892	snp	C/T	0.375	0.216506	intron-variant	Myo1e, LOC105243448	Mm_Celera	9:70208403	CTCGGAGATCGTTCC[C/T]GGTTTTGTTCTTTCC	71602
rs29739377	snp	A/C	0.444444	0.157135	intron-variant	Myo1e, LOC105243448	Mm_Celera	9:70231276	AACTCAGAAATCCAC[A/C]TGCTTCTACTTCCCA	71602
rs29740715	snp	A/G	0.244898	0.249948	intron-variant	Myo1e, LOC105243448	Mm_Celera	9:70229876	GCAGTTCAGGTGGGA[A/G]TCTTGTCACCCAGGG	71602
rs29740983	snp	A/G	0.444444	0.157135	intron-variant	Myo1e	Mm_Celera	9:70370148	GATACCTTATTATAG[A/G]ACTATGTACAAATGA	71602
rs29741434	snp	C/T	0.444444	0.157135	intron-variant	Myo1e	Mm_Celera	9:70374332	GGGTCACCACCCACA[C/T]AGATTGAGAATCACT	71602
rs29743610	snp	A/G	0.48	0.0979796	intron-variant	Myo1e	Mm_Celera	9:70316033	CATTTGCCTGAGGTG[A/G]TGCTTCGTGTATGCC	71602
rs29745191	snp	C/T	0.48	0.0979796	intron-variant	Myo1e	Mm_Celera	9:70252888	GTATATATATTACTA[C/T]GTTTTTACACTAGAG	71602
rs29749760	snp	A/G	0.5	0	intron-variant	Myo1e	Mm_Celera	9:70359622	CTGAGTCACATATAT[A/G]TCCTCCTTACTGGCT	71602

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