SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3655289 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18716414 | GCAAGTCTAGGCAAG[G/T]CCAGGCCTCAGAAGT | 218793 |
rs3656639 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18716665 | CTGCAGAATAAAACT[C/T]TGCTTTTACATACTA | 218793 |
rs3657835 | snp | A/T | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18716824 | GAAGAAAAGTCAAAA[A/T]TTATTATAAAATTAA | 218793 |
rs3660778 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18720147 | ATGAGCTCTCACATA[C/T]GTTAGCAATCCTCAG | 218793 |
rs3663068 | snp | C/G | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | Mm_Celera | 14:18736595 | TTATCATCAAGGACT[C/G]ATTAGTATTGCAGAA | 218793 |
rs3663637 | snp | A/T | 0.484429 | 0.0868505 | intron-variant | Ube2e2 | Mm_Celera | 14:18736680 | AGAGTAGTCACATGA[A/T]GTAATCTCTTTTAAA | 218793 |
rs3673697 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18795986 | CAGGTGTGGCCTTAA[G/T]GGCACCTTAAGGTCT | 218793 |
rs3673699 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18795987 | AGGTGTGGCCTTAAG[C/G]GCACCTTAAGGTCTG | 218793 |
rs3679394 | snp | C/T | 0.471655 | 0.115624 | intron-variant | Ube2e2 | Mm_Celera | 14:18612227 | TTATAGTTCTACTGT[C/T]TCAATAACCTGTGAA | 218793 |
rs3686822 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18616379 | ACCCTGAAACTCTCA[C/G]ACCTGAGGATGTTAG | 218793 |
rs3694283 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Ube2e2 | Mm_Celera | 14:18664457 | ACATTTAATATAAAT[A/G]TCACATCAGCGTCTC | 218793 |
rs3694391 | snp | G/T | 0.498866 | 0.0237825 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18664514 | TTGCAGTACTTGGAG[G/T]TTTTAGAATATGTAA | 218793 |
rs3696328 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18800323 | ACCAGGCTTATCAAG[C/T]AAATACCAACTTCCA | 218793 |
rs3709763 | snp | A/G | 0.498866 | 0.0237825 | intron-variant | Ube2e2 | Mm_Celera | 14:18664726 | TGCTAGTCATTATCT[A/G]TTATCTGTATAGCAT | 218793 |
rs3712796 | snp | A/C | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18886957 | CATGCTACCAAAAGG[A/C]TGGACATCCTACATC | 218793 |
rs3717668 | snp | A/C | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18890430 | TCAGTACACACAAAA[A/C]ACAGACACTTCAAAT | 218793 |
rs3719135 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18720001 | GACACTAGGAAAAGT[A/G]CAGCCATTCACTCCC | 218793 |
rs3719500 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18623712 | TTTAAGAGTTGTATG[A/G]GTTAAATGAATCCAA | 218793 |
rs3720675 | snp | C/T | 0.498866 | 0.0237825 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18623870 | AGAGCCAAAGCCAGT[C/T]CCAAAGGTCATGGGA | 218793 |
rs4138939 | snp | A/C | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18623949 | AAAGAAGCAGGGTTG[A/C]GGGGTTATTGCAGAT | 218793 |
rs6156883 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18726457 | CCCTCTCTCTTCACT[A/G]AGTCTGCAGTCACCA | 218793 |
rs6159611 | snp | A/C/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18726933 | CCTAGCCCATTGTGG[A/C/G]TGGTGCTATTCCTGG | 218793 |
rs6159684 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18726972 | TCCTGGGTTTTATTA[C/T]GAAGCAGACAGAGCA | 218793 |
rs6172805 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18727006 | TAGCTAATAACACCT[A/G]TCCACAGCCTCTGTA | 218793 |
rs6187783 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18806427 | tcagcttatgaatct[A/G]aggcttaggacatag | 218793 |
rs6196152 | snp | A/C | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18695701 | aaaaaaaccaatcca[A/C]agcaaaccagtagcc | 218793 |
rs6196643 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18695754 | AGCTAGAAGCAATCC[A/C]ACTAAAACCAGGGAC | 218793 |
rs6196644 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18695756 | CTAGAAGCAATCCCA[C/T]TAAAACCAGGGACTA | 218793 |
rs6196647 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18695762 | GCAATCCCACTAAAA[C/T]CAGGGACTAGACAAG | 218793 |
rs6197224 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18695855 | gaaacaaaaggagat[C/T]aagggatacaagttg | 218793 |
rs6198148 | snp | A/C | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18607570 | GCTTCATTCACATTC[A/C]AGGAATTCCAAAGCC | 218793 |
rs6198171 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18761730 | ACTCACACACTTGGG[A/G]AATGGAGGCAATATT | 218793 |
rs6210777 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18696104 | tatcctttgtgtaga[A/G]aaaggccactgattt | 218793 |
rs6211271 | snp | C/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18696182 | aagtttaggagttct[C/G]tggtgcaatttctag | 218793 |
rs6213726 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18688558 | ctgggagtgaagctt[C/T]ctctgggtgttgtgg | 218793 |
rs6220421 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18887487 | TGCATCAGGAGCAAC[C/T]CACCACCACTACCAC | 218793 |
rs6220477 | snp | A/C | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18887516 | ACCTAATGTAATGAA[A/C]TCAAGATGCATTAAT | 218793 |
rs6236872 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Ube2e2 | Mm_Celera | 14:18657044 | GTTCACAATCTTCAT[C/T]TATTTTGTGAATCTT | 218793 |
rs6237443 | snp | G/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18657132 | ACCTTTTTCTTTTCT[G/T]TTTTTCTTCTAAATG | 218793 |
rs6237459 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18657138 | TTCTTTTCTNTTTTT[C/T]TTCTAAATGAAAAAT | 218793 |
rs6240192 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18815780 | CCCTGCCTCTTGTCT[G/T]CTGGGCAGCTGTGCA | 218793 |
rs6244178 | snp | C/G | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18741597 | gtacccccagagctc[C/G]tatctctagctgcat | 218793 |
rs6245458 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18731208 | TTCTGCAATTTTAAA[A/G]ACGAGTGTACACATT | 218793 |
rs6245475 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18731220 | AAAGACGAGTGTACA[C/T]ATTGAAACCGAAAGC | 218793 |
rs6245476 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18731221 | AAGACGAGTGTACAC[A/G]TTGAAACCGAAAGCT | 218793 |
rs6270119 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18658707 | TCCCTCTGACCACTA[C/T]CAAACCTTTGTCTTC | 218793 |
rs6316653 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18741781 | aactataacagggtc[C/T]cttcggcaaaatctt | 218793 |
rs6348716 | snp | A/G | 0.498866 | 0.0237825 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18788475 | TAGATTTCAAATTTT[A/G]AGGTCAGGGGTATTT | 218793 |
rs6349270 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18788549 | ACCATCTGACATACT[C/T]CAGGCCAGCACTCAG | 218793 |
rs6376036 | snp | G/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18835761 | agagaattcaacttt[G/T]gttcctaacacccat | 218793 |
rs6376985 | snp | A/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18835878 | cacatgcatgtacac[A/T]tgtgtacgcacacac | 218793 |
rs6378206 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | Mm_Celera | 14:18836159 | TATGAAAACCTGATA[C/T]TCATAGTCATCCACG | 218793 |
rs6391387 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18741868 | gaaaagatggactat[C/T]cagagactgccccac | 218793 |
rs13459142 | snp | C/T | 0.499567 | 0.0146995 | synonymous-codon | Ube2e2 | GRCm38.p3 | 14:18574336 | CAACAGAGCGGAGCA[C/T]GACCGGATGGCCAGA | 218793 |
rs29248174 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18654662 | GAGGTTCTTTTATCA[C/T]TGAGAATAGTTTTTG | 218793 |
rs29441459 | snp | A/C | 0.32 | 0.24 | intron-variant | Ube2e2 | Mm_Celera | 14:18741649 | CCACCTATAGGGTTG[A/C]AGACCCCTTCAGCTC | 218793 |
rs29478577 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2e2 | Mm_Celera | 14:18741670 | CCCTTCAGCTCCTTG[C/T]GTGCTTTCTCTAGCT | 218793 |
rs30101868 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18820757 | TGTAGTAATGATGCA[A/G]CTCTCTTTGAGTCAT | 218793 |
rs30101928 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18599271 | AGGGTTGGGGACAAG[A/G]AAGTGGAGGAAGGAT | 218793 |
rs30102221 | snp | C/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18820152 | CTTATAAGAGAAGAG[C/G]CATTCTGCATCTCTC | 218793 |
rs30104073 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18753384 | AGTGCCTATCAAATA[C/T]AGAAGTGGATGCTCA | 218793 |
rs30104207 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18652075 | AAATATTGAAATTAT[C/T]CCATGCATCCTATCT | 218793 |
rs30106192 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18669827 | TGTGAGACACACTTG[A/G]CCCCACTAGAGCACC | 218793 |
rs30106667 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18686579 | TCTTCTCATTGTGTC[C/T]TGGATTTCCTGGATG | 218793 |
rs30108786 | snp | A/C | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18601708 | TCCAGCAAGTCTGCA[A/C]CTACACTCCTGCTAT | 218793 |
rs30109039 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18814737 | TGAATACCCAGTGGT[A/G]CCACCTAGGACCATG | 218793 |
rs30110328 | snp | G/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | Mm_Celera | 14:18826423 | GCAGTTGTTCCATAC[G/T]TGGCATGAAAACACC | 218793 |
rs30112132 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18648461 | CTTTGTAGACATGCA[C/T]GGAATATAACAAAAT | 218793 |
rs30115159 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | Mm_Celera | 14:18797511 | AAATTTAGCAGACAG[G/T]ATACAAAAACTACTG | 218793 |
rs30116845 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18798876 | AGAACCACTGTTTAT[A/G]GTCACAGGAAACAGA | 218793 |
rs30116936 | snp | A/C | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18738926 | GAGTGTGGTTAACCC[A/C]CCACTGATACCAGCT | 218793 |
rs30119475 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18885385 | AGCAAAAGAGAAAAC[C/T]GAGTCAGCTGGGCAT | 218793 |
rs30121826 | snp | C/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18816188 | GCCCCACTGAAGCTC[C/G]AGTATTAATAGATTA | 218793 |
rs30124996 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18872515 | CAGTGGACAGCCCCA[C/T]GGTCCCCAGAGGAGG | 218793 |
rs30125198 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18630218 | TATGCCAACAGAGCA[G/T]ATATGCAACCCTATA | 218793 |
rs30125327 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18759260 | CGAAAGGACTGTGAA[A/G]GATATTCTCAAAGGC | 218793 |
rs30125387 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18819386 | TATATAAGTTCAGCT[C/T]GTTTGTCATGTGACT | 218793 |
rs30125725 | snp | A/G | 0.493827 | 0.228978 | intron-variant | Ube2e2 | Mm_Celera | 14:18654689 | TTTAGGTCAGGCATG[A/G]TGATTCCACCAGAGG | 218793 |
rs30128769 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2e2 | Mm_Celera | 14:18828120 | CTGATCTCTGAATTG[A/G]GCCTCTCCCCCCAAG | 218793 |
rs30140020 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18798534 | TAGTGCTGCTCCTCT[A/G]TACCTGTGACCATTC | 218793 |
rs30140641 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Ube2e2 | Mm_Celera | 14:18819103 | AGAAGAAAGAATACC[C/T]GCAGGAAGATTGTGA | 218793 |
rs30142248 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18666471 | CTGAGCTTGTGTAGT[C/T]ACACCTTGATGCCAC | 218793 |
rs30145116 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18763089 | GTGCTACAAAGCAAC[C/T]ACAATCTGTTCTAGG | 218793 |
rs30146010 | snp | A/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18641865 | AAGTACAAAGATTTA[A/T]GTTGGTTTATGGTTC | 218793 |
rs30146011 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18790531 | GACAACTGCACAAGT[A/G]TGTGAATGTATTAAA | 218793 |
rs30146013 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18838150 | GTTTTCAAATAACAG[C/T]AGTGTGAGGTCCCTT | 218793 |
rs30149691 | snp | A/C | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18871114 | AACCAACAACCAAAG[A/C]CATAACGTAAAGCAT | 218793 |
rs30150665 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18754745 | TGCTGTGCTGGATGT[A/G]TCTTCTGACCTCCAG | 218793 |
rs30151829 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Ube2e2 | Mm_Celera | 14:18751876 | GGAAATGAAAGATCC[C/G]TATGATAAGACCTTT | 218793 |
rs30152213 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18779262 | GTTTTTAAAAGCACT[A/G]AGTTGCAGAGCAGTT | 218793 |
rs30154830 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18753852 | GACCCAGTTTTAAAT[A/G]CTATTTAAGAAACTT | 218793 |
rs30160528 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18615402 | CTCAAACTTCTTTAA[A/G]GTAGATTAATTTCTT | 218793 |
rs30161986 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18660316 | TGCACACTCTGTACA[C/T]AACCCTAGGAAGGTA | 218793 |
rs30162811 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18873762 | TGCCAGCCCAGGCTA[C/T]TATACCCAGCAAAAC | 218793 |
rs30163239 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | Mm_Celera | 14:18718129 | TGCAGTACTAAATAT[C/T]CCCCCCAAAATGTCT | 218793 |
rs30164475 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18878093 | ATCCATGGGATGGGG[C/T]ACAGGGTCCCCAATG | 218793 |
rs30164832 | snp | A/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18714364 | TAACCTGAAAACAAG[A/T]CTGAGCTCTGTGTGA | 218793 |
rs30165306 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | Mm_Celera | 14:18851819 | GCTCATGTTGGGGCA[G/T]GGGGGGCAAGATAGG | 218793 |
rs30165311 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18812143 | ATTTCGAGACACTGG[A/G]TACAGAGAGACAGCA | 218793 |
rs30166379 | snp | G/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18889096 | AATCCCTAGGCTAAG[G/T]TATACCTTTTAAGAT | 218793 |
rs30168347 | snp | G/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18836565 | TGGGGCACACCAGTT[G/T]GAACTCTATCATTAC | 218793 |
rs30168739 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18687733 | CACACTCTCACCTGT[G/T]CAAACCAGTCTAGGT | 218793 |
rs30173000 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18605042 | TCCCAGCTCAAAAGA[C/T]ACATCTTTTGGGAGC | 218793 |
rs30173938 | snp | A/T | 0.492188 | 0.0620098 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18649215 | TTAAGGCAACACTGA[A/T]GTACATAACAAAGCA | 218793 |
rs30175630 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18809307 | GTGCCCCTGATACAG[C/T]CTGTTATGTGAATTC | 218793 |
rs30179646 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | Mm_Celera | 14:18739732 | GAGTGGAGGGGGGGG[C/G]GAAAGTAAACCAAAA | 218793 |
rs30187231 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Ube2e2 | Mm_Celera | 14:18738620 | AAGTTACAATTAATC[C/T]ACTCTCCCACAGTTC | 218793 |
rs30187363 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18611821 | GAAAAGACCATTGTA[A/G]AACTCTAAGGTTAGC | 218793 |
rs30192176 | snp | G/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18594798 | CTTTATTTCATCACC[G/T]ACCAAGGAATCATTG | 218793 |
rs30192888 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18612661 | ATAAGTTTCAAAAAC[C/T]TGCTAACATATAAAT | 218793 |
rs30193162 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18746605 | TGATCCACTCTACTG[C/T]TGCGGTATTCTGGGT | 218793 |
rs30193824 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18625238 | CCAACCCGCCCACTC[C/T]TGCTTTCTGGCCCTG | 218793 |
rs30200269 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18744870 | CTTCCCTTAGTATGT[C/T]ACTGTCCAAGCAGGT | 218793 |
rs30206355 | snp | G/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18818816 | TCATGTTGGGTGATG[G/T]TTTTTTTTTTTTGTC | 218793 |
rs30206362 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18624334 | TAGAAGGGAAAGACT[A/G]GGAGATTTTGTCTTT | 218793 |
rs30207295 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18811931 | TATTTACACAAAAGA[C/T]AATATAAAAAGTGCT | 218793 |
rs30207654 | snp | G/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18795746 | TCAGGTAAAAGTGAG[G/T]GCAAAATTACTTTGG | 218793 |
rs30207873 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18646856 | GTACCGTGAACATGG[A/G]TTGGTCAGCATGGTG | 218793 |
rs30212679 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18610100 | CTTGATTCACTGATC[A/G]AACTCAGAAATCTGT | 218793 |
rs30215123 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Ube2e2 | GRCm38.p3 | 14:18896007 | CTAAGGAAATCTAAG[A/G]ATTTAGGGTACAAGG | 218793 |
rs30215552 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18842662 | CTCCACATTCACCTT[C/T]CAATCATGCCTGCTT | 218793 |
rs30222132 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18869664 | ACCAGAAGACCCACA[A/G]GGCATTCTCTCTCCC | 218793 |
rs30238715 | snp | A/T | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18745120 | CTGAACCCAAACCAT[A/T]GTGAGATATGTGTAG | 218793 |
rs30239187 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18846347 | TGTTGCCAAGGCAAC[A/G]GCCGCCATATTCCCA | 218793 |
rs30242282 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18790998 | CATGTGCCGTCACTG[A/G]GTGAAGACTTCAGAC | 218793 |
rs30243640 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18580099 | AGTTAACTACATTTA[C/T]TTAAACCTCCTTGTA | 218793 |
rs30247066 | snp | A/C | 0.484429 | 0.0868505 | intron-variant, upstream-variant-2KB | Ube2e2 | GRCm38.p3 | 14:18671581 | CATCTCTGCCTCTCG[A/C]ATGCTTGACACGATT | 218793 |
rs30251839 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18614779 | CAGAAATCTGCCTGC[C/G]TCTGCCTCCCGAGTA | 218793 |
rs30251976 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18611833 | GTAAAACTCTAAGGT[C/T]AGCTGCTCAGCCTCA | 218793 |
rs30252758 | snp | G/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18609311 | ACTGCATGGTGATCA[G/T]CAGTCAGAAATTCAC | 218793 |
rs30257923 | snp | G/T | 0.475309 | 0.108333 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18830976 | TGTCTGAAAGGAGTC[G/T]TGGTGACAGAGCAGA | 218793 |
rs30258652 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18635984 | ATAGTACTCTATTGC[A/G]CAAACGAACCACATT | 218793 |
rs30259412 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18698974 | ATGGGGAAATGTGCT[A/G]TCCCTTAGGAGGTCC | 218793 |
rs30261433 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | Mm_Celera | 14:18797515 | TTAGCAGACAGGATA[C/T]AAAAACTACTGGGAG | 218793 |
rs30262177 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18779014 | TATGCCCCCCAAACC[A/G]TTTAAACATAGCTTG | 218793 |
rs30262659 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18840120 | CCTCCACTAGATGAC[A/G]CTACAACACTTGATC | 218793 |
rs30276100 | snp | G/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18725236 | ATATAGGAGAAGAAT[G/T]ATTATTAATTATAGT | 218793 |
rs30276144 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18817553 | TGCCTTTTTACTGTC[C/T]CCGAGTTACAGAGCC | 218793 |
rs30277252 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18753111 | TTCATAGCAGCCTTA[C/T]TTATAATAGCCAGAA | 218793 |
rs30279782 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18786190 | ACTAGGAGGATCTTC[C/T]AGCGGGAGTGGCACA | 218793 |
rs30284245 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18875405 | ATTTAGTGCAGAGTT[C/T]TATCAGACCTTCAAG | 218793 |
rs30286642 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18762379 | ACAACTTCTTCTTAA[A/G]GAAGAAACGGGTTTT | 218793 |
rs30291502 | snp | A/C | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18637633 | AAAAAATCATGCCTG[A/C]AGGTCTCATTCCTTA | 218793 |
rs30292025 | snp | C/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18748922 | TTCTTTGTTAAATTC[C/G]CCCTTGACCGCTCCC | 218793 |
rs30293290 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18583069 | TGAGAGAGTAGAGAG[A/G]GAGAGAGAATATATA | 218793 |
rs30294920 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18662411 | CTTCAATGACACACC[A/G]GGACCATCTCCAGGG | 218793 |
rs30295774 | snp | C/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18820146 | ATTTTACTTATAAGA[C/G]AAGAGGCATTCTGCA | 218793 |
rs30298687 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18831500 | GCTGTATAGATATTT[C/T]CACAATGCCACCAGA | 218793 |
rs30298890 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18583593 | ATGTACACCAAAGGA[C/T]GGTTATATAGGACTG | 218793 |
rs30300516 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18727358 | TGTATATAAGTTTGG[C/T]ATTACCTTAGAGCTT | 218793 |
rs30304309 | snp | A/G/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18817647 | AGGCAGCAGTGGCTA[A/G/T]CAAGGGGACATTCCC | 218793 |
rs30305207 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ube2e2 | Mm_Celera | 14:18688089 | GATTAAAGGCATGCA[A/C]CATCAGGCCCAGCTC | 218793 |
rs30306011 | snp | A/C | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18727905 | AAAACTGTGTACCTG[A/C]TAAATTACAACTTCT | 218793 |
rs30306450 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18885329 | ACCCATTTTCTAGAG[A/G]TTACTATAAGCAAGA | 218793 |
rs30306471 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18614942 | ATAATATCCTCTTCA[C/T]TATATGAATGCGGCA | 218793 |
rs30307592 | snp | A/G | 0.625 | 0.125 | intron-variant | Ube2e2 | Mm_Celera | 14:18614686 | TTTTTTTTTTTTTTT[A/G]GTTTTTCGAGGCAGG | 218793 |
rs30309420 | snp | C/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18750540 | TAGACCAAAAGGAAG[C/G]AAATTCACCCAAGAG | 218793 |
rs30310113 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18643221 | GGATATCCAGGACCT[C/T]GGGAATCCCAGCTTC | 218793 |
rs30310375 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18578639 | ATGTAGCTCAGTCAG[C/T]CTGGAACTCAGCTAT | 218793 |
rs30311846 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Ube2e2 | Mm_Celera | 14:18644973 | ATGATTTCTGCCCCC[A/G]AAGTATATATTTTTT | 218793 |
rs30313889 | snp | A/T | 0.375 | 0.216506 | upstream-variant-2KB | Ube2e2 | GRCm38.p3 | 14:18895982 | ACCCCAAGACCGGAG[A/T]CTTGGAAGTCTAAGG | 218793 |
rs30314338 | snp | C/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18745739 | ATTTAATTTGGAAGA[C/G]GTCTTAGTTAGGATT | 218793 |
rs30315730 | snp | C/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | Mm_Celera | 14:18786303 | GTGTGTGATTGGCTC[C/G]AAGAGTTGTAGAAAC | 218793 |
rs30321840 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18869430 | TTAGGTTCATTCAAA[A/G]CCTATAGGGTGGGGT | 218793 |
rs30323446 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18669976 | CGTGGTGTGATAAGA[A/G]AAACAACTGACTTAA | 218793 |
rs30333210 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18847657 | GGTGCCATGGGTATC[C/T]TGGGCACAGACGATG | 218793 |
rs30334104 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18852341 | AAACCTGAAATAATA[C/T]TGCGCAGTTATATGT | 218793 |
rs30336300 | snp | A/G | 0.495 | 0.0497494 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18833126 | TCTCAGATATAAAAC[A/G]TGGCAGATAAGGAAG | 218793 |
rs30337131 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18839694 | TCACTGCCTCTGGCC[A/C]CACTGACCACACAGT | 218793 |
rs30338986 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18745495 | AGTAAATTGTTCATG[C/T]AATTGACAACTCACT | 218793 |
rs30339905 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18711867 | TATCTTACTTATCAC[C/T]TCAGGTATTTTTTCC | 218793 |
rs30350785 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18793070 | AGAAGCCTGAGCCTG[A/C]TGCAGGCCAGCTGCT | 218793 |
rs30353658 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18810961 | TCCAAGATTTAAGTG[C/T]GTCCTCCAAGTCTCT | 218793 |
rs30354734 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18760457 | TGTTTGTCAAATTCA[C/T]CGAACAGTCCCACAG | 218793 |
rs30354925 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18674568 | GCACCATGAAATAAG[A/G]TCAACAACAGGATAA | 218793 |
rs30358164 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18872726 | ACTCAACCAGGATTA[C/T]AGGAAGGACAGGCTC | 218793 |
rs30361419 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18674054 | CATCTTGATCCATGG[A/T]TGACTTTATTTTATC | 218793 |
rs30363084 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18844309 | CTCTTCCTCATACAC[A/G]TCGACCCTAACAGGA | 218793 |
rs30363767 | snp | A/C | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18639546 | CCCGAGTGATCAGTT[A/C]AAAAGAAGTAGGGTA | 218793 |
rs30364238 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18753640 | CTCCTGATTTTGTTG[G/T]AACAGATGTTGTGTT | 218793 |
rs30365972 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18613851 | GCAACTACCACCTGG[C/T]TTAATGTTAAAGCAC | 218793 |
rs30367635 | snp | G/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18803517 | AAAGACTCATATCCT[G/T]GAGGGTAGCAGGCAT | 218793 |
rs30368038 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18601638 | TTACCTACAGCTGGA[A/G]TCTTTCTCAGTTCCT | 218793 |
rs30368101 | snp | G/T | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18696732 | CTCTTAACATTCTTC[G/T]GTTGAGGGACATCTG | 218793 |
rs30370980 | snp | A/C | 0.455 | 0.143091 | intron-variant | Ube2e2 | Mm_Celera | 14:18641601 | TGATCGTCAGCAGCG[A/C]TTATAGAAACACTGC | 218793 |
rs30383988 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18810768 | CTTGCAGGTAGAAGT[A/G]TGGCATTTTTTGGGT | 218793 |
rs30388228 | snp | A/T | 0.429688 | 0.173817 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18699057 | GGTTACTAAGTATGG[A/T]GAGGAACTGGCCCTC | 218793 |
rs30388411 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18842603 | GGCTTACAGACTCTA[C/T]CTCTCTCCAGGGTTC | 218793 |
rs30388443 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18849920 | AAACAAAATAATACT[C/T]TGAGCATTGAGACCA | 218793 |
rs30389319 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2e2 | Mm_Celera | 14:18772837 | TAATCATTAGCTGTT[C/T]ATACTTCATATTTTT | 218793 |
rs30390206 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18746312 | TGTATCTTTATATCT[A/G]ATGTCAAAGCAGTTT | 218793 |
rs30391925 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | Mm_Celera | 14:18816274 | AACAAAGAATTTTAG[A/G]CAAAAGGGTACACTA | 218793 |
rs30393557 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18849414 | TTTAAATTTTTATTT[A/G]AGAACAACCTCTGAG | 218793 |
rs30394644 | snp | C/G | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18763317 | CTGTGTACATTTTCT[C/G]TTAGACCTAAATTTA | 218793 |
rs30394882 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18607012 | GATGATGAGGGAGGA[A/G]GAGGGAGTTGAAGAC | 218793 |
rs30396768 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18583642 | GCCATGCTATCTGAT[A/G]GTCAGAGTAAAACAA | 218793 |
rs30400646 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18674590 | ACAGGATAAAAAGGA[A/G]AAAGTGAGGAAGACA | 218793 |
rs30400996 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18661305 | TATTCCTTCTGACTT[C/T]CATTCCTCTTGACTC | 218793 |
rs30401114 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18657690 | CTGACTTTAAAGCAC[C/G]TGCTGTAAGTGGGCT | 218793 |
rs30407166 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18716290 | TAAACCAGTTGGCTT[C/T]AAACTCTGATGGATC | 218793 |
rs30407234 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18760995 | TGCCCATGTGGTGTT[A/G]CCTGGCTTCCACACA | 218793 |
rs30408414 | snp | A/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18586752 | GTATGGAAAGTTAAA[A/T]TCAATAGTAATGAGC | 218793 |
rs30411254 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18711795 | TGATGGTGACCTTGG[A/C]AACTGTGAACTTATA | 218793 |
rs30413770 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18870570 | CTGTATATGATACAT[A/G]ATGCTCATATAAGGA | 218793 |
rs30415109 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18820827 | CACCACGATGTACTT[A/G]GCGGTATGTTACTTT | 218793 |
rs30415668 | snp | G/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18709999 | TGCAAAAATGCATCA[G/T]TCCAACTTCAGAAGT | 218793 |
rs30429411 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18794560 | TCCTCCAGACCTCCA[C/T]TCAGCTCCTTGTACA | 218793 |
rs30430037 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18787707 | GCCTGTATGACAGTA[A/G]TAGCTAGAAGGCACA | 218793 |
rs30431405 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18609763 | CTGCAGCAGGGAAGT[A/G]GGGGTGCTTTTATAA | 218793 |
rs30432439 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18581019 | CCTACATACACCATG[C/T]GTTTTTTACCCAGTG | 218793 |
rs30434960 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18644203 | TAGGAATGAACTGGA[A/G]CAGCACAGATTTTTA | 218793 |
rs30436517 | snp | A/T | 0.32 | 0.24 | intron-variant | Ube2e2 | Mm_Celera | 14:18654782 | ATTTCTGGGTCTTCA[A/T]TTCTATTCCATTGGT | 218793 |
rs30440109 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18831462 | GAGATACAGTCCCAC[C/T]TGCAGCACCCTAACA | 218793 |
rs30441257 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18629370 | CCCCGACTGACAATT[C/T]TCTGCACAGTGAAGA | 218793 |
rs30442121 | snp | A/G/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18829252 | GGACAAATAGTATCA[A/G/T]TCCTCAGAGGCCACC | 218793 |
rs30443050 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18850839 | ACTGCTGAAGCAGTG[C/T]ACAGTGCAGCCTCTT | 218793 |
rs30443514 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | Mm_Celera | 14:18810132 | TCAAAGGACTTCCAG[C/T]TCCTATTATTACTAT | 218793 |
rs30446044 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18644377 | CACACACACACACAC[A/G]TAAGATGATGAATCA | 218793 |
rs30447106 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18665503 | AAAAGCAGAAATGAG[C/T]ATCTGACTTTACTGA | 218793 |
rs30447108 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18761107 | GAGTCACGAGCAAAA[A/G]AGTTTTCTGTTTTTA | 218793 |
rs30450429 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18595655 | ATTATTTTTTGCTTT[A/T]CTGAGGGGGTAGTTT | 218793 |
rs30450454 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18643341 | GGTAAACACTGTCTA[A/G]CTTGCTTCCCCAGAG | 218793 |
rs30452237 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18690411 | CCTGACCAGAGGCTC[A/G]GGTACCTTTTAATCA | 218793 |
rs30456361 | snp | A/T | 0.495 | 0.0497494 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18754422 | CACTGTCTTTGTTAG[A/T]CTATAAGATGATAGG | 218793 |
rs30457421 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18787360 | AAACCTCAGAAAGAG[C/T]GAGGCCCAAGAACAC | 218793 |
rs30458036 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18689341 | GGAAAGCTGAAAGCC[C/T]CTGGAGCACACCTTG | 218793 |
rs30458145 | snp | A/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18800262 | AGCTAGGCTATGTAG[A/T]GAGACTCTGTCAAAG | 218793 |
rs30459805 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18597225 | GTGCCACTGGTCGGG[C/T]GGAGCTCCTGGGTGC | 218793 |
rs30461634 | snp | A/G | 0.49827 | 0.0293608 | intron-variant, upstream-variant-2KB | Ube2e2 | GRCm38.p3 | 14:18671220 | TGATAGCTTTCCAGT[A/G]TTTATATTTTAACAA | 218793 |
rs30462131 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18809159 | ATTCTGATTAATGGA[A/G]CTATAAGCTCCAAAA | 218793 |
rs30465169 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18757131 | AGCTGTAAAATTATT[A/T]TTTTTTGCTACTTTA | 218793 |
rs30469640 | snp | A/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18730587 | TCTCTGATACAAAAA[A/T]CAAAAAGAAATTTTC | 218793 |
rs30484352 | snp | A/C | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18655058 | ATTGCTGTTCTATTC[A/C]GGAATTTTTTCCCTG | 218793 |
rs30486418 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18712192 | TAGCTACATGTGCTG[C/T]AACCGTGCAAGGCTG | 218793 |
rs30488590 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18708779 | AGCTCCTCCATGAGG[C/T]GAAAGAATTTCTAAC | 218793 |
rs30492950 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18639477 | GCAGCAAAGGCTAAA[A/G]ACCTGGAGTGGACAC | 218793 |
rs30492980 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | Mm_Celera | 14:18626650 | TATTGGATTTTAGTC[C/T]CCTATCTGATTTAGG | 218793 |
rs30495645 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18605899 | TGCAGCTGAGAACAA[A/G]ACAGTGTGACTTAAG | 218793 |
rs30498298 | snp | A/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | Mm_Celera | 14:18836500 | AATAATTTTAAAGCC[A/T]TCACTTAAGGACTTG | 218793 |
rs30498304 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18738823 | CTTCTTTCAGTGTAC[A/G]GACCCTATGGGTCAT | 218793 |
rs30500737 | snp | A/T | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18584854 | TATTTATTTATTTTT[A/T]AATTTCTGTGCATGA | 218793 |
rs30501232 | snp | C/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18820738 | CCATGCTTCGGGGAG[C/G]GGGTGTAGTAATGAT | 218793 |
rs30501561 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18831928 | TAGCAGAGGAATCCA[A/G]GGGCCTCATTTCAAG | 218793 |
rs30501878 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18746002 | CAGGCAACAAACTAC[C/T]CCAACAAGGCAACAC | 218793 |
rs30501917 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | Mm_Celera | 14:18754715 | TCCTTTCCCAGGAAC[A/C]CATCTATTAAGAGCT | 218793 |
rs30504499 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18595753 | GTTTTGTCATGGAAT[A/T]TCTTGGTTTCTCCCT | 218793 |
rs30504515 | snp | A/C | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18675913 | GGCAATAACAACATC[A/C]GTGGCCATTTGAGCA | 218793 |
rs30504831 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | Mm_Celera | 14:18820378 | GCCACATAAAGCCTC[A/G]CTGTGGCACATAAAG | 218793 |
rs30505494 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18647435 | CCAAACCAGCATATG[A/G]CCAGTGATGTCTCTC | 218793 |
rs30507523 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18848836 | GCTTCCTCACAAAGT[A/G]CTATGGTTTCTGGGA | 218793 |
rs30508673 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18599880 | GAACATAGATTCATG[C/T]CAATCATGTATGAAA | 218793 |
rs30509354 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18836958 | CTTTGGACATATAGG[A/G]AAGAGGACAGTGGAA | 218793 |
rs30510428 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18853479 | CTGAGGGAAGGAGCC[A/G]CTCTCCTTTGGTGGT | 218793 |
rs30512011 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ube2e2 | Mm_Celera | 14:18851838 | GGGCAAGATAGGGTT[A/C]TCAGATCAATCATTA | 218793 |
rs30517193 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18849513 | CCACCATGAGGTCTG[C/T]TGACTCCACCCCTTT | 218793 |
rs30521545 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18725684 | ATTTACTACAAACAA[A/G]ATTTCTATTTTCTAT | 218793 |
rs30522878 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18646705 | GTATACCAGGTTGGC[C/T]TCAAACTCAGAAATC | 218793 |
rs30524217 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18644345 | CACACACACACACAC[A/G]CACACACACACACAC | 218793 |
rs30524898 | snp | A/C | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18762540 | GAATTAGTTGATGGA[A/C]AGCAGAGGTGAAGGC | 218793 |
rs30525814 | snp | A/C | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18796995 | GTGGCACTTACTATG[A/C]GCAGTGGCACAGTGG | 218793 |
rs30530128 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18578164 | AGACTTCATTGTGTC[C/G]ATACTCTAAACAAGC | 218793 |
rs30530292 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ube2e2 | Mm_Celera | 14:18815596 | CTTCTATCCCCCCCC[A/C]CACACACACACACAC | 218793 |
rs30530674 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18848124 | CATTCTTAGGCCTCT[A/G]AACCTGATTGGTCAG | 218793 |
rs30530695 | snp | A/C | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18793339 | CATTTTTAAACCTGT[A/C]CTCTTATAACTCTGA | 218793 |
rs30533754 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | Mm_Celera | 14:18625157 | TTTATTTTTTATTAG[A/G]TATTTTCTTCATTTA | 218793 |
rs30542807 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18763702 | AGCATTAGTTATCTG[C/T]AGTTCTTCGTGAAGG | 218793 |
rs30543005 | snp | A/G/T | 0.625 | 0.125 | intron-variant | Ube2e2 | Mm_Celera | 14:18760878 | TGGCGGGGGGTGGGG[A/G/T]GGTGGGGGGAGGCGG | 218793 |
rs30545775 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18670601 | AGAACATTTGTTTCT[C/T]ATCCAGAAGACCTCG | 218793 |
rs30546247 | snp | C/T | 0.42 | 0.183303 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18846633 | CTTCCCAATATCTTT[C/T]TCTTATCTTCCAAAT | 218793 |
rs30546431 | snp | C/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18741976 | CACCCATTGGTCTTC[C/G]CTCTTCTTGATTTTC | 218793 |
rs30548789 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18748619 | CCATGAGAAAGCGAG[C/T]CCTTCACATTCTCCC | 218793 |
rs30551187 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18673248 | AATCCATGTAGGCAG[A/T]TGGATGACATCTAAA | 218793 |
rs30551951 | snp | A/C | 0.487535 | 0.077957 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18647341 | AATGGACTTCCTATG[A/C]AGAACTTGACCCAGA | 218793 |
rs30552193 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | Mm_Celera | 14:18611268 | TGGATTAATCTAATT[A/G]CAGGAAGAGATGTCT | 218793 |
rs30553441 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18809280 | AACACCAAGTCTGGT[A/G]CACAAAAACAAGTGC | 218793 |
rs30555476 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18606438 | GGCCTATCAAGGACT[C/T]GCTCCTGTGAGGTAG | 218793 |
rs30556119 | snp | C/G/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18661742 | GGCTGACACAAAGGC[C/G/T]GTAAAGTCATCCCAG | 218793 |
rs30556591 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18634743 | TAACATGCCACAGCA[A/G]CATTCAGTGGTAATG | 218793 |
rs30568949 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18576560 | TGCTGCAGGACCAGA[A/G]TGTGTACATTTTAAG | 218793 |
rs30577826 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18791720 | GACTGTCTGTGAAGA[A/G]CAGGATCATAAAGCT | 218793 |
rs30578226 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | Mm_Celera | 14:18745119 | GCTGAACCCAAACCA[C/T]AGTGAGATATGTGTA | 218793 |
rs30579988 | snp | C/G | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18599203 | TCCTGGAAGCTACAA[C/G]TAAAGACCCAAACCA | 218793 |
rs30587298 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18700313 | ACTGGTAGGATTGCT[C/T]AGTGGGTAAATGCAC | 218793 |
rs30587780 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | Mm_Celera | 14:18786193 | AGGAGGATCTTCTAG[C/T]GGGAGTGGCACAGCT | 218793 |
rs30588458 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18606850 | GCAAACTTTTGGATA[C/T]TACCAGCTGACCAAA | 218793 |
rs30588593 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18610163 | GTGTGCGCCACCACT[C/T]ATTGGAATGGCTGGT | 218793 |
rs30588694 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18815746 | CTCCAAGGGCGTGAC[A/G]TGAGTGAAGGAGAGC | 218793 |
rs30589608 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18628827 | TTGAGCCTGGGTCTT[C/T]TGGAAGAGCAGTCTC | 218793 |
rs30592128 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18869591 | AAGTAGAAAGTGACA[C/T]CCCCACCCACAGCCA | 218793 |
rs30593036 | snp | G/T | 0.375 | 0.216506 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18710983 | TCAAAATTCTTCAAT[G/T]TAGCCTCATGCAGAT | 218793 |
rs30597420 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18616267 | TGATATGAACTGTTG[A/G]TTTCTGTTATGAAAA | 218793 |
rs30599127 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18829268 | TCCTCAGAGGCCACC[A/C]GCTGTTTTTGAGGTA | 218793 |
rs30599550 | snp | A/G | 0.492188 | 0.0620098 | utr-variant-3-prime | Ube2e2 | GRCm38.p3 | 14:18574212 | GTAATAACAACAGGC[A/G]ACAGAACGGAGGGCT | 218793 |
rs30599718 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18763093 | TACAAAGCAACCACA[A/G]TCTGTTCTAGGTAAC | 218793 |
rs30599719 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18839069 | GGTGTGACCTGACTG[A/G]AGTAGGTGTGACACT | 218793 |
rs30601124 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18610211 | AGGCTGAAGTTTAGG[C/T]AATGTAACAATTAAC | 218793 |
rs30603569 | snp | A/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18832405 | TTAAGTGCCTGAGAG[A/T]GTGTGTAGCTTACTG | 218793 |
rs30603589 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18787461 | CTCCACTCCAAGTAG[A/G]AGCCAGCTGAGCATA | 218793 |
rs30603867 | snp | C/G/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18890211 | CATGCTTTTGAAAAA[C/G/T]GAGACTGCCTGTGAC | 218793 |
rs30605405 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18751871 | ACTAAGGAAATGAAA[A/G]ATCCCTATGATAAGA | 218793 |
rs30606508 | snp | A/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18870910 | ACTACCCAATTATCA[A/T]GCTGGCCCGAGACCA | 218793 |
rs30606868 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18757368 | GAAGCTTCAGCAATT[A/G]CTGTCCTTTCTGAGA | 218793 |
rs30607213 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18709451 | CAGCAGCCCTTAGGA[A/G]GTAATAGATACTACT | 218793 |
rs30607278 | snp | A/C | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18780383 | TAAAAGTGTCCTCAG[A/C]AATGCACAATAAGGG | 218793 |
rs30611298 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18775395 | CAAAAGGATGGACCA[C/T]CTAGAGACTGCCACC | 218793 |
rs30615441 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18814724 | AGAACAGCCTAAGTG[A/G]ATACCCAGTGGTGCC | 218793 |
rs30620073 | snp | A/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18733526 | TTGACAAGGGAGCTA[A/T]AACCATCCAGTGGGA | 218793 |
rs30621091 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | Mm_Celera | 14:18725777 | ATCTCAATTTTTTTT[A/T]ATTGTTTTTTACACA | 218793 |
rs30623540 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18838542 | TCAAGATCAAGGCCC[A/G]ATGGTCATTCTAGCC | 218793 |
rs30634548 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18848534 | AAGATCTGGCTATAG[A/G]GCATTTTTTTTTTTT | 218793 |
rs30635062 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18630081 | TAATATTGATCATAT[C/T]AACGTAGAAAAGAGA | 218793 |
rs30640994 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18625314 | CTCTCCTCCCTTTCA[C/T]GGCCTACTAGGCCAT | 218793 |
rs30643804 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18768138 | CGACCACCTTCCCAG[C/T]CAGAGGATAGGGGTC | 218793 |
rs30644323 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18817248 | CGTTCCATTGGCTCT[C/T]TCTCTATAAGAGATC | 218793 |
rs30644439 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Ube2e2 | Mm_Celera | 14:18597762 | ACTCTGAATTCATAA[C/T]GGCTCAGAACCAGGA | 218793 |
rs30644663 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | Mm_Celera | 14:18797516 | TAGCAGACAGGATAC[A/T]AAAACTACTGGGAGT | 218793 |
rs30644911 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18707086 | CTGGCATTCTCAGCA[C/T]AGAGGAAAGAGCTAC | 218793 |
rs30645734 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | Mm_Celera | 14:18667183 | TTTTGTTTTTCTAAT[A/G]TAATAAACTCCAAGA | 218793 |
rs30647606 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Ube2e2 | GRCm38.p3 | 14:18895475 | CCTTCTGCCCCAGCC[A/G]CTGTTGAGTCGTTTT | 218793 |
rs30648475 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18595346 | AAGTCAATTTTATCC[A/G]TTATTAGAATGGCTA | 218793 |
rs30648679 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18846377 | AGAATCGACTTGGCT[C/T]ACCTCCCACCTTTAC | 218793 |
rs30650381 | snp | G/T | 0.495 | 0.0497494 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18754396 | AGAGAATATATTTTC[G/T]TCCTCTTAAACACTG | 218793 |
rs30651826 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18581115 | GCAGCTTGTTAGTGT[A/G]AGTCAGGTCAGGACT | 218793 |
rs30653944 | snp | A/C | 0.35503 | 0.226867 | intron-variant | Ube2e2 | Mm_Celera | 14:18846405 | TACCTGTGACTAAGT[A/C]ATCATCCATATATAA | 218793 |
rs30654244 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18699511 | AAAATGTTATTAATC[A/G]TATAATTTATCCAAG | 218793 |
rs30654813 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18610077 | ATTATGGACTGCATT[C/T]TGCTTCCCTTGATTC | 218793 |
rs30654889 | snp | A/T | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18724332 | AGAAGGACAGGGGGA[A/T]ATTGGAATTCAGCAG | 218793 |
rs30655079 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18729700 | AGTATCCTGGGATTC[C/T]ATAATTACCTCCTCA | 218793 |
rs30655123 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18719470 | TGCTAATAGTAAAGC[A/G]TGCTGCGAAGGGAGA | 218793 |
rs30659705 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18882488 | TACCTGTCACATGAT[A/G]GTCTTAGGCCACTAA | 218793 |
rs30662359 | snp | A/T | 0.46281 | 0.131194 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18847158 | CCTAGTGAGTTAATG[A/T]GATGACAAACTAGTA | 218793 |
rs30665402 | snp | C/G/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18723621 | ACAGAGACCAAGTGT[C/G/T]GAGCAGAGACTGAAG | 218793 |
rs30670740 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18627071 | GTTTTCATTGTAGAG[G/T]GCTTTTTTAAAAACC | 218793 |
rs30672533 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | Mm_Celera | 14:18741886 | AGTCCATCCTTTCAT[C/T]TTAGCTCCAAACTTT | 218793 |
rs30672669 | snp | A/C/T | 0.31405 | 0.280505 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18664837 | TATCCATTTCCCCCA[A/C/T]GTATTTGAGAGAGAA | 218793 |
rs30672671 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18580580 | GTGGTGTACAGGGTC[A/G]AAGCAGAAAGGCTTG | 218793 |
rs30675274 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18596953 | TCTTCTGGGTTTTGT[A/G]GTACTAGCTGCTATG | 218793 |
rs30677075 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18579492 | GAGCAAGCATGTGCC[A/G]CAGCACACATGTGGG | 218793 |
rs30677326 | snp | G/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | Mm_Celera | 14:18641228 | AGCAATTTTACTGTC[G/T]TTTAAAATGAGTTGT | 218793 |
rs30680323 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18676019 | CTTTTTGTCACCTAG[C/T]CATTTACTGCCTAAA | 218793 |
rs30684140 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18743420 | TTGATGGGGATTGCA[C/T]TGACTCTGTAGACTG | 218793 |
rs30684679 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18584386 | CATTGTTGGCAGCGC[A/G]TTGGCTCCATTCTTA | 218793 |
rs30687307 | snp | A/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18837085 | CAGAAGCCTTGATAC[A/T]GCTGCCGTGCTGAGG | 218793 |
rs30687734 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18767988 | CACTCAGCATCGGCA[A/G]GAGCCATCTTGGTTC | 218793 |
rs30688338 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18778993 | GCCACTGACAGTTGG[A/G]GAGCATATGCCCCCC | 218793 |
rs30688763 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18785718 | GCACTAGTTCAGCTC[A/G]GAAATACATATTCAG | 218793 |
rs30690747 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18764072 | AAATAGATATAGTTA[A/G]AGAATATGCTGGCTT | 218793 |
rs30691742 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18870167 | AACACAGTGAGTGGG[G/T]TTATATGTCACTGGA | 218793 |
rs30693158 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Ube2e2 | GRCm38.p3 | 14:18895011 | TGAGAAAAAAAAAAT[A/G]ACAGCACCTTTGTCC | 218793 |
rs30693429 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18663830 | CGGCTCAGTCACTTA[C/T]CCTCATAGACTATGC | 218793 |
rs30693849 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18736188 | TAGAATACCATAACT[C/T]TTCATTGATTTAATG | 218793 |
rs30697120 | snp | A/G | 0.495 | 0.0497494 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18829771 | GGTTAGGATCTGCTC[A/G]GCCAGTAACTGCTTT | 218793 |
rs30697622 | snp | A/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18622931 | ATCACATCTACTTAG[A/T]CATTTCACACCTTAA | 218793 |
rs30700106 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18700200 | TTACATCAGCTAATT[C/T]AGAAAGAGCATCTTC | 218793 |
rs30700172 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18809097 | CTCTCATCTTTCCAA[C/T]GCCTAGTGCATGTTA | 218793 |
rs30701038 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18846060 | CAAGATTACCAGCCA[A/T]TGCCCACAGAAGAGC | 218793 |
rs30701329 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18611040 | GATACCAGACATATA[A/T]GTGGGACACAAATCT | 218793 |
rs30705710 | snp | G/T | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18629931 | GGCAGCACAGCACCA[G/T]GCAGGTGTGGTCACC | 218793 |
rs30707086 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | Mm_Celera | 14:18797514 | TTTAGCAGACAGGAT[A/T]CAAAAACTACTGGGA | 218793 |
rs30708085 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18830559 | TAACAGCAGGGTCAG[G/T]GATCTGCAATCAGAA | 218793 |
rs30709727 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18643222 | GATATCCAGGACCTT[A/G]GGAATCCCAGCTTCA | 218793 |
rs30717908 | snp | A/T | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18584855 | ATTTATTTATTTTTA[A/T]ATTTCTGTGCATGAG | 218793 |
rs30719077 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18816315 | TGTAACACATTACAG[A/C]TTTCACAAGATATTT | 218793 |
rs30723978 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18809693 | CTCATTGCTTCTATC[C/T]CTGGCTCCTGGCTGC | 218793 |
rs30724236 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18786453 | CCAGCCCTGCCAATA[C/T]GGTAAAATGCAGTAT | 218793 |
rs30724548 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18723708 | ACTCAGACACTATTG[C/T]GGATGCCAAGAAGTG | 218793 |
rs30725473 | snp | G/T | 0.475309 | 0.108333 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18759902 | ACAAGTAAATTCTCA[G/T]CAATAGTGCCTTACA | 218793 |
rs30725833 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18674077 | ATTTTATCCTGTTCT[C/T]AATATTCAAATAGAA | 218793 |
rs30726544 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18715252 | TTAACTGCGCACAGC[A/G]CCATTGCCTTGTCTG | 218793 |
rs30734850 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18736329 | AGCCAATTCTATCCT[A/G]AAGCTATAAGTATAT | 218793 |
rs30736773 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18661615 | GCCACTAGGCACAAT[A/G]TGATTGGCAGAACAC | 218793 |
rs30739970 | snp | C/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18844480 | CCATCCAGGGCAGCC[C/G]TTACATCTGGAGATT | 218793 |
rs30740884 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18852120 | TAAAAATAAAATGTG[A/G]CAATAGGAAGCCTTG | 218793 |
rs30742074 | snp | A/C | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18701520 | GTCACCTCTTCTCCA[A/C]GGTATCTAGGAAAAT | 218793 |
rs30751106 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18838268 | CAACACAGTCCTAAA[C/T]AGACAAGGAAGACAC | 218793 |
rs30751579 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18882894 | ACAACAAGATAACCA[A/G]AGGAGTCCTGGTCCT | 218793 |
rs30759552 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18781067 | AATATGAACTGCTAT[C/T]CTGACTGATACCAGG | 218793 |
rs30763396 | snp | A/G | 0.495 | 0.0497494 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18751954 | TCTACCATGTTAATG[A/G]ACTGGCAGGATTAAT | 218793 |
rs30765425 | snp | C/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18765403 | GCTAGGCCAATGTAT[C/G]GGATATAGGACTCAG | 218793 |
rs30766292 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18637452 | CAAGACACTGTGTGT[A/G]TATTCTCTTCTTTAT | 218793 |
rs30769721 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18736072 | CGTGCACATCCACAG[A/G]ACGCTGCCATAAGCT | 218793 |
rs30771975 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18846612 | ACTATAACATATATC[C/T]GTATGCTTCCCAATA | 218793 |
rs30775073 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18725051 | TAACACTGTATTTCC[C/T]TGGTTTCATTTTATC | 218793 |
rs30775370 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18709245 | TTATATATACATATA[C/T]GTGTATATATATATA | 218793 |
rs30776225 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18601549 | TGCCACAGCTTAAAG[A/G]CTCAGTTCTTTACAG | 218793 |
rs30776912 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18780916 | CACTGTGGCTATCCC[G/T]GCCATTGACAGGAGC | 218793 |
rs30777712 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | Mm_Celera | 14:18621215 | GCCTTTTTGTCTTAT[G/T]GACGATGTCTTTTGC | 218793 |
rs30782403 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18728314 | TAAATTAGAAAATAT[A/G]TCCTCACACTGAAAG | 218793 |
rs30784103 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18630937 | AGGGAGTATTACAGC[C/T]GACGTGATGCAGGAG | 218793 |
rs30784163 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18830292 | AGAGAAGTCTTCTTT[A/G]GTCTAAAATAATTCT | 218793 |
rs30785560 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18839162 | ATGGATGAAGACTTA[A/G]AACTCTCAGCTCTGC | 218793 |
rs30787693 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18589208 | TTGGACATAGTTCTA[C/T]GGGAAGATTCTGCAA | 218793 |
rs30787747 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18844723 | ACACCTTACCTCACC[G/T]TTTGTCAGCTGCCCT | 218793 |
rs30789824 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18826707 | AAAGCTAAGGATACT[C/T]TGCCTATCAAGTGCA | 218793 |
rs30791852 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18709932 | CTGTCATACTGGGTC[A/G]CTCCATAGAGTATCA | 218793 |
rs30792542 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18848414 | TCCTCATATCCCCTG[A/G]TTGCTTGTCTGGATA | 218793 |
rs30794378 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18667808 | GCCTGCTATGCTCAC[A/G]GGTTAAACTTACAAT | 218793 |
rs30794585 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18874446 | ACTCTGATCAATAGA[C/T]AGAACCTGAAAACAG | 218793 |
rs30796651 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18764750 | CAGGGTTTGTATTCC[A/T]GCACAGAACATCATG | 218793 |
rs30798144 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | Mm_Celera | 14:18590392 | AGGTGTGCTGTCAAG[C/T]TGCTAGTGTAAGGTC | 218793 |
rs30807665 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18699318 | AAACTGCCTTATTTA[A/C]ATATAGTTCATGCCA | 218793 |
rs30815556 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18818193 | TACCCACATAGTGGC[A/T]CACAACCATCCAAAA | 218793 |
rs30818976 | snp | A/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18636332 | TTTTATTGGTATAAT[A/T]ATGACATTTTATTAT | 218793 |
rs30822918 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | Mm_Celera | 14:18810981 | TCCAAGTCTCTGATG[C/T]GTTGACATTTAATCC | 218793 |
rs30829394 | snp | C/T | 0.378698 | 0.270641 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18833875 | CTAATCTCTATGCTT[C/T]CTTCTTTAAGTCACT | 218793 |
rs30830708 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18779537 | ACTGTTATTTAGGCC[C/T]TGCTATTCTTTTTTT | 218793 |
rs30835278 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18650584 | TTTAAAATCATATCT[C/T]ACGATGCTGGTAGAG | 218793 |
rs30837097 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18670675 | CTCTAGTTCCAGAGT[A/G]TACTCTTTGGACTCC | 218793 |
rs30839775 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18843191 | TCTATTGTCTCCAAG[A/G]GGAACAACTGAGCCG | 218793 |
rs30842257 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18634312 | ATCAACAAAGTACAG[A/G]GCTTTGCTCAAGGCC | 218793 |
rs30842367 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18610908 | TGATTCAGTGGCAAA[A/G]AATACTGGCTGAGTT | 218793 |
rs30843740 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18823055 | TTCTGGCTTCCATCT[G/T]CACCCGGAGCTGATC | 218793 |
rs30844454 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18840147 | GATCCTGCCAATGAG[C/T]CACCTCCCCTCCTCC | 218793 |
rs30844810 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18739248 | TTTAAAAAGATATCT[A/G]TACCTAGATATCAGT | 218793 |
rs30846050 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18687997 | TCTGTATAGCCCTGG[A/C]TGTACTGGAACTCAC | 218793 |
rs30846974 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18839649 | AAGACTCACAGACTT[C/T]TACCATGTTAGCTGA | 218793 |
rs30849247 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | Mm_Celera | 14:18797517 | AGCAGACAGGATACA[A/T]AAACTACTGGGAGTT | 218793 |
rs30850447 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18715271 | TTGCCTTGTCTGTAA[C/T]AGCTTGCAATGATAG | 218793 |
rs30854450 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18810474 | GGAGAGGTGATTTCC[C/T]GGGTACATGTGTCCC | 218793 |
rs30859385 | snp | G/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18732008 | CATTAACTTATTATT[G/T]GTTTCCTAGAAAATG | 218793 |
rs30861249 | snp | G/T | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18604757 | TGGTCCACAACAGCA[G/T]AGGAGTAAAATACAT | 218793 |
rs30862508 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18848664 | GCCTTATGCCTCCAA[A/G]TTCCAGTACTGTTTG | 218793 |
rs30862591 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18762840 | GAAGCAGAGGCAGGC[A/G]GATTTCTGAGTTCAC | 218793 |
rs30866465 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18875675 | CTTCATTCCAGGGAT[A/G]CAAGGATGATTCAAT | 218793 |
rs30867001 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18606621 | AGGAACAGCTAAGAG[C/T]AGACCTCTCAAACCA | 218793 |
rs30871547 | snp | C/T | 0.495 | 0.0497494 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18641957 | GCAGGAGGAGAGGGC[C/T]AAGTCCCAGAAATCC | 218793 |
rs30874417 | snp | C/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18818685 | CACATGTATCTTGTT[C/G]TGAATAGCCTTTTAA | 218793 |
rs30876119 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18706826 | TACATAATAGAGCAT[A/G]AGTAATTCAAATATC | 218793 |
rs30877312 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18728853 | CAATACCTCTCCTGG[A/G]CATATATCCAGAAGA | 218793 |
rs30878838 | snp | C/G | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18778589 | TCAAACAATACACTT[C/G]AACTTTTGAGCAGCT | 218793 |
rs30880008 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18774087 | CCTCTAACTGTCAGG[C/T]TATGCCTCCCTTTGG | 218793 |
rs30881299 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18762273 | CCTATGGGCAGTCAC[C/T]AGACTGCATCATTTA | 218793 |
rs30889134 | snp | G/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18584113 | AATTTTCCTGCCTCA[G/T]CCCCTATGTTCAGGG | 218793 |
rs30889312 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18814868 | TCTGGGCTGCTACCC[A/G]TGGACATATTGATAT | 218793 |
rs30890211 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | Mm_Celera | 14:18826357 | CTGAATTGCACATTT[A/T]AAAATAAATTTTATT | 218793 |
rs30892224 | snp | G/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18622341 | TGAAAAAAATCAACG[G/T]AAATAGTTACCTGAA | 218793 |
rs30894239 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18727755 | GTGGGAACATTTTGT[C/T]AATTGATGTTCTCTT | 218793 |
rs30895643 | snp | A/C | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18704641 | AAAGATCACTCTTAT[A/C]CTGATAGGAATATCA | 218793 |
rs30896339 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18679600 | AGTTTGAAACTGAAA[C/T]GAACCCCCCTGGAAC | 218793 |
rs30896517 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ube2e2 | Mm_Celera | 14:18786998 | ACATACACACACACA[A/C]AAAAAAACCCACATA | 218793 |
rs30896911 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18849404 | TACGTTCTTCTTTAA[A/G]TTTTTATTTGAGAAC | 218793 |
rs30897832 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18773505 | ATTCTTAAACAAGGG[A/G]AAAAAATCAAAGCTC | 218793 |
rs30898374 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18831755 | TAGCACCCTGAACTG[C/T]GTGCTCCCTGGTGAT | 218793 |
rs30898848 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | Mm_Celera | 14:18624646 | ATTATGTGCATGACA[A/G]TCACCTAGGCAGGGC | 218793 |
rs30900658 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18756617 | TCTCTTTTCCTTCTA[C/T]GTGGATTCCTCCGTC | 218793 |
rs30909797 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18776234 | CTTGAGCTACAGTGT[A/G]TGTGTGTGTGTGTGT | 218793 |
rs30914150 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | Mm_Celera | 14:18701644 | AATGGCCTTTCTCTA[C/T]ACAAAGAATAAACAG | 218793 |
rs30915582 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18811297 | AGTACTGGTGACTTG[A/G]TAAGAGGGAGAAAAA | 218793 |
rs30916674 | snp | C/G | 0.5 | 0 | utr-variant-3-prime | Ube2e2 | GRCm38.p3 | 14:18574068 | CTGCAGTGGGGGAAT[C/G]CCAAATCTTTCAAGT | 218793 |
rs30920263 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18659687 | TCTGGTCCCACTTGG[C/T]AATATCTTTGCAAAT | 218793 |
rs30921150 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18803606 | GTGTGCTTGGGCATA[C/T]CCACATGTACCATAG | 218793 |
rs30923337 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18832291 | GGTTCCAATGAAGCT[A/G]TCCCCATAGCCTATG | 218793 |
rs30928415 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18636701 | CTTCCAGAGTTGCTC[C/T]ATTTCCCAGGTACAA | 218793 |
rs30930607 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18599508 | AACAGATTCATCACA[C/T]CCGCATGAATTCACA | 218793 |
rs30935506 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18870937 | ACCAGCACTGGCAGG[A/G]AGTTATTTTCTCTTC | 218793 |
rs30936966 | snp | C/G | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18773591 | ACCCACTGTATCATT[C/G]TCCCTTACACTGAAG | 218793 |
rs30938953 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18676639 | GCTTTCATTTACGTT[C/T]CACGGTAGTTGCAGT | 218793 |
rs30939821 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | Ube2e2 | GRCm38.p3 | 14:18574202 | AGTTTAAAATGTAAT[A/G]ACAACAGGCGACAGA | 218793 |
rs30941670 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18817300 | CCTATACGCCCCATT[C/T]CTTCTCCCCTATGAA | 218793 |
rs30942631 | snp | C/G/T | 0.625 | 0.125 | intron-variant | Ube2e2 | Mm_Celera | 14:18797925 | CCTCTCTCCCTCCCT[C/G/T]TGTTTAAAGGCGTGT | 218793 |
rs30944205 | snp | A/T | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18584987 | GTTATCTGCAAGAGC[A/T]AGTGTCACCTCTCTA | 218793 |
rs30944216 | snp | C/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18717186 | CACACTGTACCACCC[C/G]AGCCTGCCCCTGAGT | 218793 |
rs30945113 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18793069 | AAGAAGCCTGAGCCT[C/G]CTGCAGGCCAGCTGC | 218793 |
rs30945726 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18811510 | TTAGACATGATCTCA[C/T]TATATAGCCCAGGCC | 218793 |
rs30945736 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18611041 | ATACCAGACATATAT[A/G]TGGGACACAAATCTC | 218793 |
rs30945833 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | Mm_Celera | 14:18787258 | CTCCTTCTCTTTTTG[A/T]GTTTGCTTCCTAGCC | 218793 |
rs30948036 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18597249 | TGGGTGCCTGGGTCC[C/T]GCTGGTTTCAGTTAC | 218793 |
rs30949344 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18773943 | AGAACCTTGAGTTTG[C/T]TACTTTCTGGGACTA | 218793 |
rs30949388 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18751250 | AGGCTTCATCTCAGG[A/G]ATGCAAGGATGGTTC | 218793 |
rs30949670 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18714282 | CTCTTTCTTCTTCTT[C/T]TTCTTTTTTTTTAAA | 218793 |
rs30949708 | snp | A/C | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18625044 | TTTGTAATAAGAACT[A/C]TCTTTAAAATTTTCA | 218793 |
rs30955401 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18705939 | GGAAAAAAAAATCTC[A/C]AGGAGGTTACTACGT | 218793 |
rs30956759 | snp | G/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18636339 | GGTATAATAATGACA[G/T]TTTATTATTAAAATG | 218793 |
rs30957655 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18872781 | AGCACTAGAGATAAT[C/T]AGATGGTGGGAGGCA | 218793 |
rs30959442 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18884939 | CACTCCAGGCTTTGA[A/G]ATAAAACTGCTCTCA | 218793 |
rs30961033 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18704433 | TTTTGGAATGAAGCC[A/G]TATCTTGTTTGTTGT | 218793 |
rs30968304 | snp | C/G | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18791634 | CTTTTAACAGTTGAG[C/G]AGCTTAAAAAACATG | 218793 |
rs30968361 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18844235 | CTAAACTTGAGAGAC[C/T]CTCTCATTGGGTCCA | 218793 |
rs30969349 | snp | C/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18699047 | CTTAAGGAATGGTTA[C/G]TAAGTATGGTGAGGA | 218793 |
rs30971319 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18833382 | AATAACTTCCCAAAA[C/T]CATACTGAGAAGACC | 218793 |
rs30973031 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18614241 | GGTGGAACCATCTGA[A/G]CTGTGAGATTTTCTT | 218793 |
rs30973220 | snp | A/C | 0.46875 | 0.121031 | intron-variant | Ube2e2 | Mm_Celera | 14:18771612 | GCTATCGGGTGCACC[A/C]TTAAAAACTTAAAAA | 218793 |
rs30978106 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18809740 | TAAGCCTGGGCCTCT[A/G]AACTGTAGGAGCAGA | 218793 |
rs30978947 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18723288 | ATAGCCAGAAGCTGG[A/T]AAGAACCCAGATGTC | 218793 |
rs30984804 | snp | G/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18885901 | CTTGACAACAAACCT[G/T]CATTTCTTAAACCAC | 218793 |
rs30989179 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18762153 | TGTCAGCAGAGACAC[A/G]AGGCACCCAAGGTTT | 218793 |
rs30989657 | snp | A/C | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18745936 | CCAAAGACAGCTAGC[A/C]GAAGACTGACTTCCA | 218793 |
rs30990886 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18838673 | ACATAAGCAGGCCCA[A/G]GGACTCACTGTGCTT | 218793 |
rs30992378 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18658522 | GTGTGTAGAGAACAG[A/G]CAGAGCTCCACTATG | 218793 |
rs30993592 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18627650 | TCTTTCTTTCTTTCT[C/T]TCTTTCTTTCTCTCT | 218793 |
rs30994579 | snp | C/G | 0.375 | 0.216506 | upstream-variant-2KB | Ube2e2 | GRCm38.p3 | 14:18895978 | CTACACCCCAAGACC[C/G]GAGACTTGGAAGTCT | 218793 |
rs30995073 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18764939 | GGCTTGCTCAGCTCA[C/T]TTTCTTATAGTACCC | 218793 |
rs30995177 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18601842 | CTCGTGAACCCTGAT[C/T]ACCTCTCGTTAGATC | 218793 |
rs30995582 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18614809 | ACTGGGATTAAAGGC[A/G]TGCGCCACCACGCCT | 218793 |
rs30996786 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18576988 | CTGGCTGTACTGGAA[C/T]TCACTCTTTAGACCA | 218793 |
rs30999840 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18827402 | CCAGGCTGCACATGG[C/G]GAAGACTTGAACACA | 218793 |
rs31003551 | snp | A/C | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18637287 | TGAAGCTAGAGCAAG[A/C]CAAAAATGACACACA | 218793 |
rs31005651 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2e2 | Mm_Celera | 14:18655030 | AGTGGGGAAAAGCCT[C/T]GAAGATATGGGCACA | 218793 |
rs31006282 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18767947 | ACTAAGGCTGATCTT[C/T]AATAACAACATAAAT | 218793 |
rs31008698 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18836926 | TTTAAGATGAGGAAA[A/G]AGTGAGGGAAGGGCC | 218793 |
rs31010982 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18854337 | ACACACACATACACA[C/T]ATGCAAGAAAGAACA | 218793 |
rs31016070 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18756543 | ACACAGAAGCTCTGA[C/T]AGAGCCACAAAGGCT | 218793 |
rs31017264 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18641758 | TAATTATCTAGTGTT[C/T]TTTTTCTGTTCACAG | 218793 |
rs31018004 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18818637 | GTGCCACATAACAAG[A/G]CCCTGTCACCACCAA | 218793 |
rs31018155 | snp | A/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18828757 | CCAGAATTTACTTCT[A/T]AAGTCATGCTAGCAA | 218793 |
rs31018171 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2e2 | Mm_Celera | 14:18720462 | TCCAACTATCCCCTA[A/G]CCCCCCAACTGAATG | 218793 |
rs31020375 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18589162 | GTGGGATTGCAAGCT[G/T]GTACAACCACTCTGG | 218793 |
rs31020867 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ube2e2 | Mm_Celera | 14:18757700 | GCAGTACACAATTGC[C/G]TGTTAATTGTTGTTC | 218793 |
rs31024038 | snp | C/T | 0.498615 | 0.0262793 | downstream-variant-500B | Ube2e2 | GRCm38.p3 | 14:18573160 | AGAGGAGTTTGTTTA[C/T]ACTGAAATGATGGAG | 218793 |
rs31026469 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18889080 | CCATTGAGCTACCTG[C/T]AATCCCTAGGCTAAG | 218793 |
rs31029746 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18829748 | TTGACCCATCTGTAG[A/G]AAACTGAGGTTAGGA | 218793 |
rs31040029 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18704181 | GCATTTATTTCTGGT[A/G]TCTTATCTCTTAGCT | 218793 |
rs31040050 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18760286 | TTAATTACAAAACTT[A/G]AAAACTTTTTCCAAG | 218793 |
rs31040369 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Ube2e2 | GRCm38.p3 | 14:18895531 | TTGGGGATGTTGTGA[C/T]GTCAGCTTCCACTCA | 218793 |
rs31040789 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18610153 | GGGATTAAAGGTGTG[C/T]GCCACCACTTATTGG | 218793 |
rs31043623 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18660829 | ATGGAACAGATATGA[C/T]AGATGGGAGTTTGAA | 218793 |
rs31044044 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Ube2e2 | Mm_Celera | 14:18672477 | AAGTAGATATTAGTC[C/T]GTAATTTTAAGATTG | 218793 |
rs31045007 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18839964 | CGGATGGGTTTAAGA[A/G]ATCTCCATACATACT | 218793 |
rs31046234 | snp | A/C | | | intron-variant | Ube2e2 | Mm_Celera | 14:18815598 | TCTATCCCCCCCCCC[A/C]CCACACACACACACA | 218793 |
rs31046524 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18817236 | GCCCAGCACTTTCGT[C/T]CCATTGGCTCTTTCT | 218793 |
rs31047117 | snp | A/C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18844006 | TTTCACCTAAATGCT[A/C/T]TCCCCTCCCAGACTC | 218793 |
rs31047181 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18665982 | TTACAATTTGGAGGT[A/G]AGCTAAAAGTTATCA | 218793 |
rs31047485 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | Mm_Celera | 14:18848605 | CCTAGGGCTGGTGGT[A/T]CTGGGTTTATAAGAC | 218793 |
rs31050228 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18855507 | TCCACTCCACAGGAC[C/T]CCTAGCACACCCATG | 218793 |
rs31058636 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18744738 | AGAGGGTTCGTTTAG[A/G]GACCTATATGAGTAA | 218793 |
rs31058638 | snp | A/C/T | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18599181 | CAGCTAAATGAGCTA[A/C/T]GAAAATTCCTGGAAG | 218793 |
rs31066332 | snp | A/C | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18676353 | GAAATCCCAGTCAAA[A/C]AAGATATATTTGTAT | 218793 |
rs31068347 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18871301 | GCCCTGTAACCCCAA[C/T]ATATCATGAGGGCAT | 218793 |
rs31069032 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18597638 | AAGACCAGCTAGTTT[G/T]GGCTAAGCAGTAGTT | 218793 |
rs31069882 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18791898 | ACAGGTTTGAGTTGG[A/G]CTGGTGAGTCTGGTT | 218793 |
rs31074734 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18669989 | GAAAAACAACTGACT[C/T]AAGTTATAGTGTTAT | 218793 |
rs31075229 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18762152 | CTGTCAGCAGAGACA[C/T]AAGGCACCCAAGGTT | 218793 |
rs31085166 | snp | C/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18890287 | CAAGGGTAAAACACA[C/G]ATACATGGGGAAGGG | 218793 |
rs31089520 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18711537 | GCACACCCCTAGTGG[C/T]GCACTTTCGTCAACA | 218793 |
rs31089523 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18842870 | AAGCTGGCTATGCCA[C/T]AGTGTCAGACATCAA | 218793 |
rs31090536 | snp | A/C | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18759594 | TGTCATTAATCTGCT[A/C]TAAGTGTCAGTGTTT | 218793 |
rs31092103 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18660987 | CTGAAGGAGAGGTGG[C/T]GATCTTGGGTAGCCC | 218793 |
rs31093566 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18605744 | GTTTAACTTGAGCTA[A/G]GAGAGCTGACGATAG | 218793 |
rs31093770 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | Mm_Celera | 14:18869680 | GGCATTCTCTCTCCC[C/T]CCTCTGTGAGAGCTG | 218793 |
rs31093908 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18793196 | GCCATGGGGACAACC[C/T]ACTGATCCTTACTGC | 218793 |
rs31095983 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18760867 | ATACTTGAATGTGGC[A/G]GGGGGTGGGGGGGTG | 218793 |
rs31096640 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18764360 | TCTTCAGGGAGGAGG[C/T]AGTCAGGTTAGTTCC | 218793 |
rs31096838 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18836468 | TTTATTTATATGGCA[A/G]TGATAATCATGGTAA | 218793 |
rs31097465 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18829558 | CCTTAACCCTTTCTT[C/T]AGTTCAGGATGATAG | 218793 |
rs31097477 | snp | A/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18839080 | ACTGAAGTAGGTGTG[A/T]CACTGTGGGTGTGGG | 218793 |
rs31103452 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18767895 | ACATATACAAGAAGA[C/T]TGAAATAATCCCATG | 218793 |
rs31105022 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18705755 | AGCATTGCCCGGAGA[A/G]GCAGGCAACTCAGAT | 218793 |
rs31105991 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18711805 | CTTGGCAACTGTGAA[A/C]TTATAACCCTGAAAA | 218793 |
rs31115510 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18631740 | AGAGAGAAGCCCAGG[A/G]TGCCTGTTGTCAGTA | 218793 |
rs31116586 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18800763 | GAGGACTGAAAGAAG[A/G]GACCACTGCTAACTG | 218793 |
rs31116880 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18830369 | TTTTTATGTAAATAT[A/C]AATAACAGAAAACAA | 218793 |
rs31119781 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18650586 | TAAAATCATATCTCA[C/T]GATGCTGGTAGAGGA | 218793 |
rs31121053 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18780903 | CAATCAATGATGTCA[C/T]TGTGGCTATCCCTGC | 218793 |
rs31124820 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | Mm_Celera | 14:18608598 | TGTATCTTCTTTAAA[A/T]AAACAGTAATGGAAA | 218793 |
rs31133300 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18823614 | TTCTCCTGTATTTCT[C/T]TAAATACAGGAGAAC | 218793 |
rs31133999 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18748779 | ATCCAAGGACATGAG[C/T]TACACCTGAGCCCGG | 218793 |
rs31135170 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18687472 | CAGAAGATGAAGGCC[C/T]GAAACAGGGCTTATC | 218793 |
rs31135377 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18830942 | TGTGCTTCCAGGCCT[A/G]TTAGGACCAGTTTCC | 218793 |
rs31138169 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18598243 | CCTGTTCCATTGCTC[C/T]AGCATGGTGGGTCCC | 218793 |
rs31138258 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18673715 | AACTTGGGATATAGT[A/G]CCTATGAGAAAAACA | 218793 |
rs31141931 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18638675 | AACAGGTCCACTACC[A/G]CAGTATCCTTTCTTT | 218793 |
rs31141933 | snp | A/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18732344 | GTAAGTATATACCAA[A/T]ATAATTATATATATC | 218793 |
rs31143686 | snp | A/T | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18794443 | TGTTTGCACATGCAA[A/T]CGCCAAGCACTCATA | 218793 |
rs31144250 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18797142 | CAGTGGTAGGAAAAC[A/G]CTAGTAACTGTGAAG | 218793 |
rs31146962 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Ube2e2 | GRCm38.p3 | 14:18895890 | ATTCCAGAAAGCAAC[A/G]GCCAGTCAAGTCCCA | 218793 |
rs31149064 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18649152 | TATCCATTCACCACC[C/T]GCCACCTGACACAAC | 218793 |
rs31152342 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18719544 | AACATGGTAAGTCTG[A/G]TAAGATGTTCCTAAA | 218793 |
rs31153622 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | Mm_Celera | 14:18688065 | CTGCCTCTGCATCCC[A/G]AGTACTGGGATTAAA | 218793 |
rs31154081 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18656707 | ATCAAACAGAAGCTC[C/T]ATGTCTGTCTGTCTC | 218793 |
rs31159717 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18749882 | TCAAAGGAAAAATCT[A/C]CCAAGATGAATGCTC | 218793 |
rs31160832 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18605651 | CAACAACAACAATAA[C/T]AACAACAACAACAAC | 218793 |
rs31165406 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18744983 | CTGCCTTCAGAAATG[C/T]AATCCTCATGTTCTT | 218793 |
rs31169436 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18794077 | GGTGGAGACTTGTGG[C/T]CAGCCAGTCAAATGA | 218793 |
rs31169494 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18687255 | CTTACATTTGCTTTT[C/T]GCCATCTGGTAATCT | 218793 |
rs31170738 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18833341 | CTGAAATTTCAGTAT[C/T]TTTCAAATAGTCCCT | 218793 |
rs31172050 | snp | A/C | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18831274 | CAAACAAAAAAAAAA[A/C]AAAGGAGTGGTTGTA | 218793 |
rs31174966 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18819384 | TTTATATAAGTTCAG[C/T]TCGTTTGTCATGTGA | 218793 |
rs31177093 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18748819 | CCAAGGCTGTTAAGG[A/T]GCATCTATGTTCCGG | 218793 |
rs31177667 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18709241 | AATATTATATATACA[C/T]ATACGTGTATATATA | 218793 |
rs31181005 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18772856 | CTTCATATTTTTTCT[A/G]AAGTCTGTCAAGCAA | 218793 |
rs31181908 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18875016 | GAAATCAACCAAGTG[A/G]AAACAAAAAGAACTA | 218793 |
rs31186533 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18665315 | TGGCTTTTATACTAA[C/T]TCCAACCATGTATCA | 218793 |
rs31187499 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18714285 | TTTCTTCTTCTTCTT[C/T]TTTTTTTTTAAATTT | 218793 |
rs31189028 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18705871 | TGATATCCCTGTTCT[C/T]AGAGCTCACAGTCAG | 218793 |
rs31189225 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18659692 | TCCCACTTGGCAATA[C/T]CTTTGCAAATGGTTT | 218793 |
rs31189233 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18892903 | GATGTCTCTCTAATG[C/T]GGCCTTAATTTCCTT | 218793 |
rs31190648 | snp | A/C/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18644339 | CACACACACACACAC[A/C/G]CACACACACACACAC | 218793 |
rs31192544 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18848074 | ACCAGTTCTGCTCAG[C/T]CCACAGTGGGGAATG | 218793 |
rs31192547 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18609872 | CTAGATTCTCTTCCC[C/T]GCTCCCGAGCTCTGC | 218793 |
rs31194577 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18890201 | TCAGCTCAGACATGC[C/T]TTTGAAAAACGAGAC | 218793 |
rs31194619 | snp | A/C | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18791092 | AGTCTGCTCAGTTCA[A/C]TTTTTCTTTTCATGC | 218793 |
rs31195540 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18704447 | CATATCTTGTTTGTT[C/G]TGCATTTGGCCCCTA | 218793 |
rs31197311 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18760866 | CATACTTGAATGTGG[C/T]GGGGGGTGGGGGGGT | 218793 |
rs31197693 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | Mm_Celera | 14:18609445 | CAAACCCAGTGAAAC[C/T]CAGAACTGAGTATGG | 218793 |
rs31198414 | snp | G/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18670367 | TAATCCTAGCACTTG[G/T]GTGGCAGAGGCAGGC | 218793 |
rs31199094 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18659822 | TTGGTTCCAAGCACC[C/T]ATGCTAGATGGCTCT | 218793 |
rs31203483 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18788988 | ATGATGGTTGTATCA[A/G]GAGATGCATTGCTGT | 218793 |
rs31209256 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18853199 | TTGTTCTGTTAAATG[C/T]TCACCCTGTCCAACT | 218793 |
rs31214579 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18667643 | GTCACTTGAGGCTCC[C/T]TCTTCCCAAATGATT | 218793 |
rs31218859 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18686587 | TTGTGTCCTGGATTT[C/T]CTGGATGCTTTGAGT | 218793 |
rs31227031 | snp | A/C | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18831267 | AAACAAACAAACAAA[A/C]AAAAAACAAAGGAGT | 218793 |
rs31228170 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18642047 | GAGTTACACATCTCT[C/T]ACAGAAGCACAGCCC | 218793 |
rs31228378 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18763710 | TTATCTGTAGTTCTT[C/T]GTGAAGGGTTGAGGC | 218793 |
rs31232066 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18844059 | ATTCTCTCCTATGGA[A/G]CTTTGCTGACCACCA | 218793 |
rs31232675 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18817291 | TTCATATTGCCTATA[C/T]GCCCCATTTCTTCTC | 218793 |
rs31233154 | snp | G/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18662024 | GAACCCCTAAATTTT[G/T]AGCCTTAGGGTCGAC | 218793 |
rs31235912 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18637453 | AAGACACTGTGTGTA[C/T]ATTCTCTTCTTTATC | 218793 |
rs31236984 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18602782 | CTTTCAATTGTTGTC[C/T]AGTGCAGTGCCTCGC | 218793 |
rs31237342 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18701521 | TCACCTCTTCTCCAC[A/G]GTATCTAGGAAAATG | 218793 |
rs31237789 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18657636 | GGGTTGTTGATGGCT[G/T]GTCTTTGAGCTGTAA | 218793 |
rs31238578 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18650525 | GCACTCCCACTTCAG[C/T]CAGTCCTAGATACTC | 218793 |
rs31240068 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18674161 | GGCGTTTTTCAGTAA[A/G]TAACACAATCTTGAG | 218793 |
rs31240712 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18736336 | TCTATCCTGAAGCTA[C/T]AAGTATATCTGTCTA | 218793 |
rs31242613 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18679809 | GCTAGGGGTCAGCAA[A/G]TGTGAGTGCTCTTTA | 218793 |
rs31243294 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18851044 | AGCAGTCAGAGCAAA[C/T]TCAGATGTTAGAGAC | 218793 |
rs31245417 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18749928 | TGCTCCAAATACAAG[A/G]GCAGCCACATTCATT | 218793 |
rs31245508 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18598952 | AGAAAACAGGCTGCC[G/T]TTCGTAGTCCCACAA | 218793 |
rs31245914 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18714267 | CTTCTCTCTCTCTCT[C/T]TCTTTCTTCTTCTTC | 218793 |
rs31246307 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18812139 | AGTGATTTCGAGACA[C/T]TGGATACAGAGAGAC | 218793 |
rs31254370 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | Mm_Celera | 14:18627113 | GTATATTTTAAATAT[C/T]ATATTTGATTTGAGA | 218793 |
rs31258580 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18714279 | TCTCTCTTTCTTCTT[C/T]TTCTTCTTTTTTTTT | 218793 |
rs31260990 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18820391 | TCACTGTGGCACATA[A/G]AGCCTCTGCTGCCAC | 218793 |
rs31261414 | snp | A/C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18739314 | GAAAGTGACATCCAC[A/C/T]TTGTGCTCTCAATTC | 218793 |
rs31262151 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18844753 | TGACTCTGATGTTGC[C/T]ATGACTCCATACCTT | 218793 |
rs31267477 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18762183 | TTTGATGTAAACAGA[C/T]GAATGTTCTGAGAGA | 218793 |
rs31271817 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | Mm_Celera | 14:18615672 | GACCATTTGACTGAC[C/T]ATTTCAACATTATAT | 218793 |
rs31273193 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | Mm_Celera | 14:18725776 | TATCTCAATTTTTTT[A/T]TATTGTTTTTTACAC | 218793 |
rs31275266 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18828312 | TCTGCTGCCCCATCC[C/T]TCCTGCTGAGAAGTA | 218793 |
rs31275271 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18837945 | AAGTTAAAGAAGGCA[A/G]ATGCTGAAGGTCTTA | 218793 |
rs31276455 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | Mm_Celera | 14:18704445 | GCCATATCTTGTTTG[C/T]TGTGCATTTGGCCCC | 218793 |
rs31279211 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18745486 | GGACTGAGAAGTAAA[A/T]TGTTCATGTAATTGA | 218793 |
rs31282153 | snp | A/T | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18758428 | AAATAATGAATAAAG[A/T]ATTTTTTCCAATGGT | 218793 |
rs31282582 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Ube2e2 | Mm_Celera | 14:18830207 | AAGACTCCAAATTCA[C/T]TCAATGTTGGAAAAA | 218793 |
rs31283668 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18872844 | TACTTGGCATCATCA[A/G]AACCCAACTCTCCCA | 218793 |
rs31283972 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18711472 | ATCCAGATTCACAGA[C/T]AGGAGGGAGAAGTGA | 218793 |
rs31286150 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18773866 | GACAACTCTCCACTT[C/T]TTTTGGCTGGCATGA | 218793 |
rs31286264 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18609567 | AGCATAGAAACCTGA[A/G]ATTCTTCATGCTAAT | 218793 |
rs31286943 | snp | C/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18728669 | AAGAGAGGGGACATC[C/G]GCTAAGCTGGCTTTT | 218793 |
rs31287274 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18873489 | ACCAAATCATTTGGA[C/G]AAGAAATTCTCCCAA | 218793 |
rs31287941 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18731911 | ACTTAAAATTACACA[C/T]GCTTGATTCTAACAA | 218793 |
rs31288137 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | Mm_Celera | 14:18827232 | CTACACACAAACAAC[C/T]GAGGACCCAGACAGA | 218793 |
rs31288428 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18846004 | CCCTTGAATGACAAA[C/T]ACAAAAAATTTCTAA | 218793 |
rs31289151 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18705019 | ACAACACTTGGTGCT[A/G]GAACTGATACCCAGG | 218793 |
rs31289824 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18848230 | GATAGCATGAACACA[A/G]CTACTTCTGACATGT | 218793 |
rs31289918 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | Mm_Celera | 14:18604384 | TAGGGGTTCAAAGAC[A/G]AGCATACACACTCCC | 218793 |
rs31293136 | snp | C/G | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18850776 | TGGCTATGCAGATTA[C/G]CAAAGCCTGTCCAAG | 218793 |
rs31293795 | snp | G/T | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18599090 | AGAACCCAGTATCAT[G/T]TCAGGCCACTCCACA | 218793 |
rs31298879 | snp | A/C/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18699159 | TGCTCTAAATTCCCC[A/C/T]GCATTACTGCTGGAA | 218793 |
rs31302238 | snp | C/G | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18748821 | AAGGCTGTTAAGGTG[C/G]ATCTATGTTCCGGAG | 218793 |
rs31302257 | snp | G/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18665451 | CTGTGAGCAGTGGCT[G/T]TGTCACTTTACCTCC | 218793 |
rs31302853 | snp | A/C | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18739494 | CTGTCATCTTTGCCA[A/C]TCCAGAGGCTATGGA | 218793 |
rs31307494 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18848511 | CTCAACTGAGAAAAC[A/G]CCTCTATAAGATCTG | 218793 |
rs31312186 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18614089 | CTGCTGTGATAACAA[A/G]AGTCTTGAGATTGAA | 218793 |
rs31318366 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18846325 | ACACAGGTGTGAACT[A/G]CACACCTGTTGCCAA | 218793 |
rs31320205 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18838439 | GGCACTGATCTACTT[A/C]TGCCTTATTAAAAAT | 218793 |
rs31330391 | snp | C/G | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18776450 | TTTGCCATAGTTTTT[C/G]ATGCCCCAAAGACTA | 218793 |
rs31331013 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Ube2e2 | GRCm38.p3 | 14:18895269 | TTCAAGAATACAGAA[A/G]TAGCAGAGCCTTGAC | 218793 |
rs31331473 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18839065 | AATAGGTGTGACCTG[A/G]CTGAAGTAGGTGTGA | 218793 |
rs31335462 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18829003 | TATATTCACCCATCA[A/G]CATGAAGAGGCTGAG | 218793 |
rs31336892 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18607043 | CTACAGTGCTGGACT[C/G]CAGTCAAGGCTCCAT | 218793 |
rs31337441 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18842981 | TGGCACAGGGACAAT[C/T]CCTCAACATCTACAC | 218793 |
rs31340640 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18579916 | AACTCTAGCTTGGCT[A/G]GCACCTTAAGCATGA | 218793 |
rs31343362 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18727828 | AGCACAAAATACATT[C/T]TCAATTTTGTAGAAA | 218793 |
rs31351490 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18750503 | GCCTAGAGAGAGTAC[A/G]CACTAGCACATCCAA | 218793 |
rs31354875 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18603667 | CCCAACTCAGGCTCA[C/T]CTCCCTCCCTCTCTC | 218793 |
rs31355622 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18639476 | AGCAGCAAAGGCTAA[A/G]AACCTGGAGTGGACA | 218793 |
rs31355937 | snp | A/C | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18729963 | TCTGGAGACAACAAA[A/C]CAGAACAGAGGTTAG | 218793 |
rs31359169 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18746056 | CCCAAGCATACACAA[A/G]CCATCATATTCCACT | 218793 |
rs31363936 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18831115 | AGTGCTAAAGCAGTT[A/G]CCAACTGCCAGCCTG | 218793 |
rs31364823 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18759569 | TTAGCAGCTGAATTC[A/G]GTAAAACACTGTCAT | 218793 |
rs31370086 | snp | A/C | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18775410 | TCTAGAGACTGCCAC[A/C]CCATCCCATAATGAG | 218793 |
rs31375666 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18839500 | CACTGGAGAAACAAC[A/G]TCATGTGGACAGCTG | 218793 |
rs31376722 | snp | G/T | 0.495 | 0.0497494 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18849890 | CTCACCACTTAAAAT[G/T]ATGGCAAACTGGAAA | 218793 |
rs31377654 | snp | A/C | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18760748 | GAGCCAAACACCTCA[A/C]AGTTCAAGGGATCTA | 218793 |
rs31382786 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18773946 | ACCTTGAGTTTGCTA[C/T]TTTCTGGGACTACAT | 218793 |
rs31384142 | snp | A/T | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18629295 | GCTTGCATAAGTGGA[A/T]TGTGGATTGTGGCAA | 218793 |
rs31385231 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18749119 | TCCATGAACACACAA[A/G]AAGCCTAAAAAGCTC | 218793 |
rs31385597 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18578141 | ATATGGAACTTAGGT[A/G]CAATATCAGACTTCA | 218793 |
rs31386499 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18869727 | GGAACCAAAGGACAA[A/G]ACTTTGTATCTGATC | 218793 |
rs31387128 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18708458 | AGTAGCCAATGAGTA[C/T]AGGGGCCAGGAAGGA | 218793 |
rs31388143 | snp | A/C | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18622484 | GTTGAGTGGAAGCCG[A/C]CTGAATAGATAACAC | 218793 |
rs31393015 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18844370 | AGACCACCTACATTG[C/T]CCCCAATCCCTGGAA | 218793 |
rs31396457 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18589444 | TGAAGGAAGGATCAT[C/T]CAGAAACTGCCCCAC | 218793 |
rs31402193 | snp | C/T | 0.493827 | 0.0552116 | downstream-variant-500B | Ube2e2 | GRCm38.p3 | 14:18573216 | CAGAACGAGCACAAA[C/T]TGTGTTAGGAGAAAG | 218793 |
rs31402435 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18636718 | TTTCCCAGGTACAAG[A/G]GCCTCAAAGCAGTGA | 218793 |
rs31407372 | snp | G/T | 0.475309 | 0.108333 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18800167 | AAATGTCCCAGTGCA[G/T]ATCAAAGGAAAAGGT | 218793 |
rs31410163 | snp | A/C | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18818511 | AAAACAAAAAAAACA[A/C]ACAAACAAACACCAT | 218793 |
rs31412665 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | Mm_Celera | 14:18775631 | GCAACCCTATAGGTG[A/G]AACAACATTATGAAC | 218793 |
rs31413386 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18599276 | TGGGGACAAGAAAGT[A/G]GAGGAAGGATGGCAG | 218793 |
rs31414562 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18700075 | TATCAGAGCAGTCAA[A/G]GGTTATGGCAGGATC | 218793 |
rs31416591 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18768047 | AGTGAGTATGCACTA[A/C]AGAAGCTAATAGCTT | 218793 |
rs31421560 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18785707 | CAGACAAGAGGGCAC[C/T]AGTTCAGCTCGGAAA | 218793 |
rs31423083 | snp | G/T | 0.487535 | 0.077957 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18832257 | TGCTGCTCTTCCTGA[G/T]TTAGTAATCTGGAGA | 218793 |
rs31423108 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18718092 | TGCTATGATATATAG[C/T]CCCTCCCCCACAGCT | 218793 |
rs31427893 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18774354 | TGTGTTACTATGTAA[C/T]TTATATGTTGAAATT | 218793 |
rs31427972 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18690480 | CCACAGTTCTCAAAG[G/T]AGACAACACTTCCAG | 218793 |
rs31430425 | snp | G/T | 0.375 | 0.216506 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18576534 | TCTGTTGGGAAAATA[G/T]GTCTAAGACATGCTG | 218793 |
rs31430689 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18823046 | ACAGGATACTTCTGG[C/T]TTCCATCTGCACCCG | 218793 |
rs31433847 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Ube2e2 | Mm_Celera | 14:18750812 | ACAAAAGGCTATACT[A/C]AAAAAAAAAACCCCT | 218793 |
rs31433877 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18623967 | GGTTATTGCAGATGG[C/T]GAGAAGAGTGACTAT | 218793 |
rs31434508 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18626317 | GATTAAGGATGTTGC[A/G]CCAGGTGGTGGTGGC | 218793 |
rs31436541 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18590428 | AGTTTCTTTTTGGAG[A/G]CACTCAGAGCTATGA | 218793 |
rs31440209 | snp | C/G | 0.487535 | 0.077957 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18738602 | CCCACCATGGGAACA[C/G]GTAAGTTACAATTAA | 218793 |
rs31442684 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18751230 | ATCATCTATCATGAT[C/T]AAGTAGGCTTCATCT | 218793 |
rs31442697 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | Mm_Celera | 14:18601415 | CCCTTTGTCTCCCCC[C/T]CAACAATACAGAATA | 218793 |
rs31445837 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | Mm_Celera | 14:18631601 | GAACTATAATAATAA[C/T]CAGCATTGGCAAGAT | 218793 |
rs31449531 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18675161 | ATTAGAATAAAAACA[C/G]TGCCTTAATTTACGG | 218793 |
rs31450916 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18840273 | TCCCCTCCTTCTGTG[A/C]CAGCTGCAGGCTGCT | 218793 |
rs31451687 | snp | G/T | 0.375 | 0.216506 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18839570 | AGACTCCATCTGCTG[G/T]CACCTGCTGTCATCC | 218793 |
rs31455235 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18636648 | CTCTACACCTTAGGA[A/G]AATTTATCAAACACC | 218793 |
rs31458213 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | Mm_Celera | 14:18844183 | CTCTCCCAAATGGAG[A/G]GCCCTTTTAAGGTAT | 218793 |
rs31463263 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18888029 | TAAATCAAATTATAC[G/T]TTTATAATGTCCTAC | 218793 |
rs31465234 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18645520 | CTATAAAAGCCAAAG[A/G]TTCAGCAGGGATGTA | 218793 |
rs31472607 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | Mm_Celera | 14:18725509 | AGCAGTGACTACAAT[C/T]AACTTTTGAATAGTC | 218793 |
rs31473125 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18885892 | TCTTGGAACCTTGAC[A/C]ACAAACCTTCATTTC | 218793 |
rs31474139 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18832719 | ATCTTTTTTTTTAAG[A/G]ACAAAACCAATTATT | 218793 |
rs31475176 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18760484 | ACAGCCCCCAGAGGA[A/G]GTACCACTCCAAGGT | 218793 |
rs31476886 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18591337 | CCTCTCCGCCCTGCT[C/T]CCCTACCCACCCACT | 218793 |
rs31476994 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18741690 | CACAGGGCCCCCAAT[A/G]GAGAAACTAGAGAAA | 218793 |
rs31478109 | snp | A/C | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18819031 | AAACAAAAACCACCA[A/C]CAACAACAACAACAA | 218793 |
rs31478113 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18744469 | GGATCCAAACAGTCC[C/T]ATTTCCCCTAAAGAA | 218793 |
rs31480989 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18753747 | CTGTCAGTCGAGTTC[A/G]GGCCCAAGGAGGCCT | 218793 |
rs31481517 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18648478 | GAATATAACAAAATC[C/T]ATTTTGTATAATTAA | 218793 |
rs31482069 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18890037 | CCTTCTCCAATCTCA[C/T]TGTATTATAATCAGC | 218793 |
rs31484050 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18589406 | ATGGAAGGAGTTACA[A/G]AGAGAAAGTTCGGAG | 218793 |
rs31486526 | snp | G/T | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18851428 | GGCAGAGGCCCTCTC[G/T]TAAGGATTAGTTCTT | 218793 |
rs31486530 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18842821 | TATTCCTGGTATACA[A/G]ATGGAAGCTCCTTTC | 218793 |
rs31488149 | snp | G/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18735952 | AATGTTTCAGAGTTT[G/T]ATTCCAATGGGCATA | 218793 |
rs31488195 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18839966 | GATGGGTTTAAGAAA[C/T]CTCCATACATACTGC | 218793 |
rs31488208 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18603916 | GGCATCTAAAAAACA[C/T]GATTTGACTAGAATG | 218793 |
rs31488798 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18836363 | AAGTTTATGATTTTA[C/T]TAGAAAATGTAGCAT | 218793 |
rs31489094 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18661919 | TTTAGAGTTATTGTC[C/T]CGACCCGCACATACT | 218793 |
rs31491656 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18746375 | ACTGCAACAAACTTC[C/T]TTCTCTTGTGCTTGC | 218793 |
rs31495602 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18846652 | TATCTTCCAAATAAA[C/T]TCCGCCAAGTGGCCA | 218793 |
rs31495737 | snp | G/T | 0.487535 | 0.077957 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18774443 | GGAAATGACTTGTAC[G/T]ATGTCACAGTGCCCG | 218793 |
rs31496350 | snp | C/G | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18810853 | ATTGCTGTTCGAACT[C/G]TTTGTTCAGTCCCTT | 218793 |
rs31498447 | snp | G/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18639851 | CATGAGGCAAAAGAG[G/T]TTCAAGGAAGCTCTC | 218793 |
rs31506496 | snp | A/T | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18827447 | CCAATTTGAAATATA[A/T]AATATAGGAATAAAT | 218793 |
rs31507901 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18840290 | AGCTGCAGGCTGCTC[C/T]AAACGCCCTGCATTG | 218793 |
rs31511023 | snp | A/T | 0.498615 | 0.0262793 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18612621 | ATTCTGTGTAACCTG[A/T]GATGGGTAGTTATTG | 218793 |
rs31512766 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18606542 | ACAACTTATCAATAA[C/T]GTGTGTAATTGGGCT | 218793 |
rs31520331 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18660131 | AAGACAGACCCAATA[C/T]ATAACTCATGGCTAG | 218793 |
rs31523645 | snp | A/G/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18652495 | AAAAAAAAGGAAAAT[A/G/T]AAGCCACAACATACC | 218793 |
rs31523785 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18641640 | GGGTCTCAAACACTC[A/G]CATGGTCCAGTTCCT | 218793 |
rs31524984 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Ube2e2 | GRCm38.p3 | 14:18895486 | AGCCACTGTTGAGTC[A/G]TTTTGTTGTTCTGTC | 218793 |
rs31525542 | snp | A/C | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18773774 | TCAGGTTTATTGGAC[A/C]AGTGACCAGCTGCTC | 218793 |
rs31527582 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18605592 | AAGTGAGTTCCAGGA[C/T]AGCCAGGGCTATACA | 218793 |
rs31528400 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18842884 | ATAGTGTCAGACATC[A/G]AGGTAGTGGAGGCAC | 218793 |
rs31532312 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | Mm_Celera | 14:18817410 | ATACATGTGTATGCC[G/T]TCTCTCCTGTCTATG | 218793 |
rs31532586 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18712261 | CCATTTAAAAATGTT[G/T]CAGTGTTCAGGTCAT | 218793 |
rs31533251 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18673612 | GATACCTTTTAATCT[A/G]TTAGAGAAGCTGACT | 218793 |
rs31534670 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18844793 | CCTGTCTTTGGCATG[A/G]CAAACTGTTTTAAGA | 218793 |
rs31535214 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18885164 | AGCCCCTAAGTGAAA[A/G]GCCCTTTTCCTGAGT | 218793 |
rs31535388 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18811578 | AAGGCTATAATTACA[A/G]CAGTGCAATTAATAG | 218793 |
rs31537991 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18579447 | TTTTCTCAAAACTTA[C/T]TATTTACCTCTGTGT | 218793 |
rs31538070 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18869729 | AACCAAAGGACAAAA[C/T]TTTGTATCTGATCTA | 218793 |
rs31538573 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18750437 | CAAACTTATGGGATA[C/T]AATGAAAGCAGTCCT | 218793 |
rs31539659 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18823456 | AAAACCAAAAACAAA[C/T]AAAAAACAAGGCTAC | 218793 |
rs31544812 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Ube2e2 | GRCm38.p3 | 14:18896014 | AATCTAAGAATTTAG[A/G]GTACAAGGAAATCTA | 218793 |
rs32688360 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18751550 | CTTTTCAACATAGTA[C/T]TTGAAGTATTAGCCA | 218793 |
rs32960749 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ube2e2 | Mm_Celera | 14:18654724 | ATGCAGTTTTTATCA[A/C]AATTGCTCTGTAGTA | 218793 |
rs33463576 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18588961 | AACAAAGAATTCTCA[A/T]TTGAGGAATATGGAA | 218793 |
rs33858317 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18630030 | TATTTTACACTTACA[C/T]GGCTGGAATATGGTA | 218793 |
rs33858441 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18644378 | ACACACACACACACG[C/T]AAGATGATGAATCAC | 218793 |
rs33884237 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18581381 | GTTTCTTACTGGCTT[C/G]CTTCCCCTGGCTTGC | 218793 |
rs33884541 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ube2e2 | Mm_Celera | 14:18581387 | TACTGGCTTCCTTCC[A/C]CTGGCTTGCTCAGCT | 218793 |
rs33884584 | snp | C/G/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | Mm_Celera | 14:18581458 | CACCACCCACAATGG[C/G/T]CCCTCCCCCCTTGAT | 218793 |
rs36242441 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18822214 | ACAGCTCCTAATTAA[C/T]ACACAAAAGTATCAG | 218793 |
rs36244100 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18628596 | GTCTCGCCTTTCTAT[C/T]TTGATTGATCAGGTG | 218793 |
rs36247702 | snp | A/G | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Ube2e2 | Mm_Celera | 14:18671546 | AACTAAGTCTGAGAT[A/G]CTGTAGCAGAAATAA | 218793 |
rs36250399 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2e2 | Mm_Celera | 14:18802930 | CTTGTTTAAATCTGA[C/T]GTTATTTTTCCATTG | 218793 |
rs36251196 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2e2 | Mm_Celera | 14:18772122 | CAGCTGGATGAAATA[C/T]AGAATTCGAGGCTAC | 218793 |
rs36253780 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Ube2e2 | Mm_Celera | 14:18842366 | GCCAACTGGGACCTT[A/C]TTTTGCACCTGTAGC | 218793 |
rs36256462 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18611436 | TCTACTGTCTCTGTG[A/G]ATTGCTTAACATTGG | 218793 |
rs36260167 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18822383 | ACTCACAAGGCTGGA[G/T]TTAAGAGCCTAGCAC | 218793 |
rs36263086 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18677612 | AGACCAAATTCTAAG[A/G]TGAAGAACACTTGTG | 218793 |
rs36266210 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18727466 | TTGTTGTAAACAATA[C/T]CTAACACTTTCCATG | 218793 |
rs36273487 | snp | A/T | 0.497041 | 0.0383476 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18802817 | CTGCAGGGGCCAGCA[A/T]CTGACAATCCAAGTC | 218793 |
rs36273879 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18822280 | CCTTTGAAACTGAAG[A/G]AGGTAATTTAAGACT | 218793 |
rs36276158 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18808738 | GAGCCAGACTCACAG[C/T]CCTAAAACAATATCA | 218793 |
rs36277961 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2e2 | Mm_Celera | 14:18637002 | GAACAATTTGGTTCT[C/T]TAAAAGTAGCAACCT | 218793 |
rs36279925 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | Mm_Celera | 14:18872196 | TAGCACTAACCAAAA[A/G]TTTTAGTTTAATTAC | 218793 |
rs36280372 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Ube2e2 | Mm_Celera | 14:18581490 | CTAATTGAGAAACAG[C/T]ATACACGGTAAGGTT | 218793 |
rs36280690 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18780127 | CTGCCAGGGGTCTGA[C/T]TCTAAACTTGGCTTT | 218793 |
rs36284068 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Ube2e2 | Mm_Celera | 14:18839534 | CCACCATCACCGCTT[A/G]CAGCCACTGCTACAT | 218793 |
rs36290122 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18885369 | CATTCCAAATCACCA[C/G]AGCAAAAGAGAAAAC | 218793 |
rs36290138 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2e2 | Mm_Celera | 14:18732173 | AATACTGGCATATAG[C/T]CAAAGGTTCAGTTTC | 218793 |
rs36292060 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18615130 | GATGTGACTTTAAAC[C/T]CTGAAGTTATAAAAA | 218793 |
rs36292261 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18835700 | AAGATTTAAGAATCT[A/G]GGAGTTGAGGGTGTT | 218793 |
rs36293761 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18803457 | ATTGGTAGGAAGGGT[A/G]AGCAGAGTATGAACA | 218793 |
rs36296475 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18822010 | TCCTACAGTGTCTTT[A/G]GGGTAGCTGTATCCT | 218793 |
rs36298276 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Ube2e2 | Mm_Celera | 14:18678294 | GTGCTGGAGAGAAAG[C/G]CTGGCAGGTTCAGCT | 218793 |
rs36300264 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18827233 | TACACACAAACAACC[A/G]AGGACCCAGACAGAC | 218793 |
rs36300282 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18664217 | ATATAGTGACAACAA[C/T]ATGGAAACATTTCTA | 218793 |
rs36309519 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18833947 | ATTGCACTAATCACT[A/G]TACTAACAATAAAAA | 218793 |
rs36310851 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18826744 | TTTCAAACAATTTTA[C/T]TATTAACTTCAGTAG | 218793 |
rs36313337 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18796333 | ACAAGCAGTTTTTTT[C/T]TCCATTTCAAAATAA | 218793 |
rs36314087 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18799192 | AGGTGAGATACTTTC[A/T]GGAAGGAACAGAAAT | 218793 |
rs36317239 | snp | A/T | 0.21875 | 0.248039 | intron-variant | Ube2e2 | Mm_Celera | 14:18886557 | GTTTCGAGATGAAAC[A/T]GCATAAGATCTCAAC | 218793 |
rs36319208 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18613631 | ACGAGGTGCCAATTC[C/T]TTCCTAGCAGCAACC | 218793 |
rs36320741 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18772232 | ATAATTTTGTGGATG[A/C]AGACAATCTTATCCA | 218793 |
rs36325348 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18821885 | TAGGGCCAAAGACAT[A/C]CAGATTTCAGATTTG | 218793 |
rs36328505 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Ube2e2 | Mm_Celera | 14:18802722 | ATACTATTGACCTTC[A/G]AAGACTGCAGAAAAT | 218793 |
rs36330784 | snp | C/G | 0.497041 | 0.0383476 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18792233 | TACCTCCCCAAAAGA[C/G]GAAAGAAGCTCTTAA | 218793 |
rs36336374 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Ube2e2 | Mm_Celera | 14:18637581 | AAAGCTTTTCAGTGC[C/G]TTCCACAAAATCAGA | 218793 |
rs36339256 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18792039 | ACTAACTCCAAATCA[C/T]GGATATCACAGCACT | 218793 |
rs36341390 | snp | G/T | 0.375 | 0.216506 | intron-variant | Ube2e2 | Mm_Celera | 14:18619319 | CTTTAAAATGTATTT[G/T]AAAAAGCAAACAACA | 218793 |
rs36341419 | snp | A/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18801811 | CACCCCATTCACCAA[A/T]CAGGAATTTTTGCCT | 218793 |
rs36345427 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Ube2e2 | Mm_Celera | 14:18629504 | GGTGGGAGGAGCATG[G/T]AAAGTGTGAAGGCTG | 218793 |
rs36348957 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2e2 | Mm_Celera | 14:18628983 | CAGATCTAAAACCCA[C/T]TGACATTCAGGTCGT | 218793 |
rs36351275 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18677774 | CAGTGGATCAAAGGG[C/T]ACAAGTCTTGTCCAT | 218793 |
rs36352716 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e2 | Mm_Celera | 14:18881554 | ATTAAAAAGAAATTA[A/G]AACTGCTGGGACTAT | 218793 |
rs36353823 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18808272 | TGCAGATATTGAAAT[C/T]CATTTTGTTAACTAT | 218793 |
rs36355792 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18678971 | GCCAGGAACTAAAAT[A/C]TAAATCTAAAATTAA | 218793 |
rs36357492 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18801274 | CTCAGAGCTACATTT[A/G]GGAAGCAGACATTTA | 218793 |
rs36358687 | snp | C/T | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Ube2e2 | Mm_Celera | 14:18671875 | ACAATCTGAAATTCT[C/T]GGATGCTTACACACG | 218793 |
rs36360885 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18678505 | TTTGTGTGTCTTAAC[A/G]TTTATGAGCAGACGT | 218793 |
rs36365976 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18614073 | AAATTTAGCCTGTTT[C/T]CTGCTGTGATAACAA | 218793 |
rs36366057 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18755665 | GTCTGAAACACAATA[A/T]CAACCCAAAAGTCAT | 218793 |
rs36371371 | snp | G/T | 0.497041 | 0.0383476 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18649359 | CCTTATAAACTCCAT[G/T]GCAGTAAAACAGGAT | 218793 |
rs36372799 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18756817 | ACAGGTCAGACTTCC[C/T]ATACTTATTTTCTCT | 218793 |
rs36375901 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18676637 | AAGCTTTCATTTACG[A/T]TCCACGGTAGTTGCA | 218793 |
rs36376603 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18636462 | TTGTATCAAGGTTAA[A/G]GTTAGGAGAAGAGGA | 218793 |
rs36377486 | snp | G/T | 0.18 | 0.24 | intron-variant | Ube2e2 | Mm_Celera | 14:18579897 | TCTCCAGTTTTCCCT[G/T]CCCAACTCTAGCTTG | 218793 |
rs36378272 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2e2 | Mm_Celera | 14:18837949 | TAAAGAAGGCAGATG[C/T]TGAAGGTCTTACTCT | 218793 |
rs36379046 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18807083 | ATGAAATCCACAGTG[C/T]TTGTTATAAAGAAAT | 218793 |
rs36380499 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18807018 | ATTAGGCAACATTTA[C/T]TAAAACTCTTCAAAA | 218793 |
rs36381679 | snp | A/T | 0.473373 | 0.11227 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18619451 | TCATTTCCTCTTGAC[A/T]GTTGACTCTTACTTC | 218793 |
rs36388233 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18836231 | CATAAAATAGTAGAG[A/G]CTATCATCCCTGAGA | 218793 |
rs36397372 | snp | C/T | 0.42 | 0.183303 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18619232 | TGCTCCTTGCCTCCA[C/T]GTTCCTGGGCTGCAC | 218793 |
rs36399151 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18879909 | TAGAACACTTGGCCA[A/G]ATATCTAAAGCCTTG | 218793 |
rs36400023 | snp | G/T | 0.197531 | 0.244432 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18842300 | ACTTGACTTGTCCTT[G/T]TTCCCTCTATGTAAC | 218793 |
rs36401666 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18835640 | TTTAATCTATTTAAA[A/G]CTATTTCTACTTAAT | 218793 |
rs36409900 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18835157 | CCTCTGGGCATCAGG[C/T]TTCGTGCACTGAACT | 218793 |
rs36410956 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18831142 | CCTGTCTTCCCATCT[C/T]AATAACCTCCAGAAG | 218793 |
rs36411494 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18832747 | ATTTGGCAGAACTAA[C/T]GATAACCGTTGGGAG | 218793 |
rs36420971 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ube2e2 | Mm_Celera | 14:18632928 | TCTTGCTGCCAAAAG[A/G]GCACACTCTTCAGAT | 218793 |
rs36422554 | snp | A/T | 0.18 | 0.24 | intron-variant | Ube2e2 | Mm_Celera | 14:18846861 | GTTAAAAATTAATGT[A/T]AGAGCTTCTCAAGAA | 218793 |
rs36427131 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18738333 | AAATTCAAGCCTGGT[A/T]TGTTGGCAGATACTT | 218793 |
rs36430553 | snp | A/T | 0.21875 | 0.248039 | intron-variant | Ube2e2 | Mm_Celera | 14:18575212 | ATCAGAGCAGTCACC[A/T]GAAAAGAGATTAACA | 218793 |
rs36435358 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18663648 | CCTATCTAGATTGAC[A/C]CACTGCTCTAAGGGA | 218793 |
rs36436580 | snp | A/T | 0.486111 | 0.0821678 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18760299 | TTGAAAACTTTTTCC[A/T]AGTTCATTCTCATTC | 218793 |
rs36440107 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ube2e2 | Mm_Celera | 14:18849852 | AGACTTTCCTGTGTG[A/C]CAAGTTGTCACACTG | 218793 |
rs36440626 | snp | G/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18602651 | CCAAGTTAGGGTACT[G/T]CTTCTGTAATGTGAC | 218793 |
rs36451528 | snp | C/T | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Ube2e2 | Mm_Celera | 14:18673037 | GTGTGTACAGGCACA[C/T]ATGAAAGTGTTCATG | 218793 |
rs36451584 | snp | A/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18600024 | TGACCCTGTTCATGT[A/T]TGGAAAGAGGAAAAC | 218793 |
rs36456689 | snp | C/T | 0.18 | 0.24 | intron-variant | Ube2e2 | Mm_Celera | 14:18704048 | CACACAAAGACTATC[C/T]ATTTTTACTGGCAGT | 218793 |
rs36459725 | snp | A/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18600782 | AGAGACCATGGTGAT[A/T]GAATGTGCAGACTAT | 218793 |
rs36463922 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18819578 | CCAGATTCCAAAAGA[A/C]TCATTAACTGACATT | 218793 |
rs36465922 | snp | A/G | 0.18 | 0.24 | intron-variant | Ube2e2 | Mm_Celera | 14:18706870 | TTGGGCAATTTAGGA[A/G]CAGCTGTACTACTGA | 218793 |
rs36472526 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18679756 | GGATTTGGCTTTAAA[C/T]AAACAAGTCTCTTGT | 218793 |
rs36477248 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18781185 | TAAACATAACTCAGT[A/G]TATAACAATGTCATC | 218793 |
rs36479614 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18619213 | GCATGGCAACTCCTA[C/T]ATGTGCTCCTTGCCT | 218793 |
rs36490881 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ube2e2 | Mm_Celera | 14:18666926 | AACAACCTGCTGAGT[A/G]CAGGCTGAACACTGT | 218793 |
rs36491906 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Ube2e2 | Mm_Celera | 14:18586149 | ACTTCCCTATCTGGT[A/G]AACTAAAAATATTTC | 218793 |
rs36492130 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18664784 | AGGATACTGTGTGTG[A/G]AATTATAAAATTAAT | 218793 |
rs36496917 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18837057 | AGGGCAGCAGAGCTG[C/T]TGGCGTTTACCACAG | 218793 |
rs36503621 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2e2 | Mm_Celera | 14:18731899 | TTCTAAGACAGAACT[C/T]AAAATTACACACGCT | 218793 |
rs36506822 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18834125 | TCTTATATGCAAATG[C/T]CAATTTGACAACATT | 218793 |
rs36511768 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Ube2e2 | Mm_Celera | 14:18629925 | TGTGATGGCAGCACA[C/G]CACCATGCAGGTGTG | 218793 |
rs36516552 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18744771 | ACATAGCTATAGTTA[C/T]ACTGACATTGCCAGA | 218793 |
rs36518326 | snp | A/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18883302 | TATCTGTCCTCATTT[A/T]CAGGATAAGACTGGT | 218793 |
rs36520033 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18665389 | CTCAAATACAAACAG[C/T]TCAGAAGTGTCACAA | 218793 |
rs36520349 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Ube2e2 | Mm_Celera | 14:18629895 | ATCAAAATATCACCA[C/G]AGTTTCGTGGCTGCT | 218793 |
rs36521415 | snp | A/T | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Ube2e2 | Mm_Celera | 14:18672941 | TAGCCAAGCATTTTT[A/T]AAAAAGATCTTATTT | 218793 |
rs36523175 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18669140 | AAGCGGCCTTTGAAA[C/T]GGTTCACATTAACCA | 218793 |
rs36535997 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2e2 | Mm_Celera | 14:18604395 | AGACAAGCATACACA[C/T]TCCCAGCATTAACTC | 218793 |
rs36539404 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Ube2e2 | Mm_Celera | 14:18707142 | GGACATCCTAATGCA[A/G]GTTGTTGCATATTGG | 218793 |
rs36540606 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | Mm_Celera | 14:18869228 | AAAACCACATATTTT[A/T]CCTTTCTCAAGAACA | 218793 |
rs36554533 | snp | A/T | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Ube2e2 | Mm_Celera | 14:18671118 | TCCTTCTTCAACAAT[A/T]TTCAACTACAACACT | 218793 |
rs36557805 | snp | G/T | 0.197531 | 0.244432 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18849059 | GCCACACCAGACTTC[G/T]TCCCACATCCTAAAC | 218793 |
rs36562261 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18698239 | TTTCATTCATCTCAT[C/T]AGAGTCTAGAATTAG | 218793 |
rs36562936 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18808912 | ATGAGCCATAGGTTA[G/T]AATGAGCCAAAACTT | 218793 |
rs36565885 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | Mm_Celera | 14:18872042 | CTGGAAACGATTCTC[C/T]CCTCAGTTTGAGCCA | 218793 |
rs36568120 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18834088 | ACAAGCTAAGCTTAG[A/G]CAAAGCTATATAACT | 218793 |
rs36568253 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Ube2e2 | Mm_Celera | 14:18706773 | AAAGAAGGGATTCCT[C/T]GCAAGTTCAGGTGGT | 218793 |
rs36569626 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18632768 | ACAGTTAACACCGTG[A/C]ATCGCAGAGGGAATC | 218793 |
rs36573075 | snp | C/T | 0.18 | 0.24 | intron-variant | Ube2e2 | Mm_Celera | 14:18705822 | TCTGTCAGAAGCACA[C/T]CCAGCTGAAGCCACA | 218793 |
rs36583667 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18801020 | TTAAGTCATGCATCT[A/G]TTTAAAAAAAACTAT | 218793 |
rs36592623 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18642087 | TATAATTCTTACTTC[A/G]TCCCACTTCACACAC | 218793 |
rs36593381 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18601909 | ATTCTCCAGGACTTT[G/T]CGATCACAAATAAAG | 218793 |
rs36593498 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Ube2e2 | Mm_Celera | 14:18705891 | CTCACAGTCAGGCCT[A/G]GGTGGTTTCAAGACT | 218793 |
rs36595553 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ube2e2 | Mm_Celera | 14:18889169 | CAGCAAAGTTCAACC[A/G]CCAGCATTTACAAAA | 218793 |
rs36595594 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18668800 | AGTGCATTTTTGTAG[C/T]GTGCTCATCACAACA | 218793 |
rs36602051 | snp | C/G | 0.396694 | 0.202437 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18755851 | TTGGAAAATTTCTTA[C/G]ATATGTATTTAATAT | 218793 |
rs36608948 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2e2 | Mm_Celera | 14:18668353 | AATTTTGAGATGGCC[C/T]TCATGTATCTTAGCC | 218793 |
rs36611517 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18677790 | ACAAGTCTTGTCCAT[C/T]ACAGATAATGGATCA | 218793 |
rs36612522 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18632233 | TGAGGAAGGGGTCGT[A/G]GAAGAAATTGGAAGA | 218793 |
rs36614382 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18781451 | CCTCCTCCAGAGAAA[A/G]TCCTCTACCCTGTTC | 218793 |
rs36617953 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18659535 | GTGGACTTGACAAAG[A/G]GTAAGAAGGCTTTGG | 218793 |
rs36619801 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18791668 | TGGATTATAGGACAA[C/G]GACAACAAGGCCAAC | 218793 |
rs36621982 | snp | G/T | 0.165289 | 0.235211 | intron-variant | Ube2e2 | Mm_Celera | 14:18847837 | ATTTTAACCTGCACT[G/T]AGAATGTTCCTAAGC | 218793 |
rs36625060 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | Mm_Celera | 14:18834295 | ATTTCAGAATTTATT[C/T]TTGCTGGGTATAGTG | 218793 |
rs36627393 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18600316 | ACAAACAGTTAAACA[A/G]ATACGTACCATTTAA | 218793 |
rs36628670 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Ube2e2 | Mm_Celera | 14:18706845 | AATTCAAATATCATC[A/C]GCAAATCTCTTGGGC | 218793 |
rs36629927 | snp | C/G | 0.473373 | 0.11227 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18803159 | GAGAGAGGCCTTTGT[C/G]TTTTCTTAAGCAGGT | 218793 |
rs36637679 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18664467 | TAAATATCACATCAG[C/T]GTCTCACATTATTCT | 218793 |
rs36638194 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Ube2e2 | Mm_Celera | 14:18634352 | AAATGTAACCCATGT[A/C]CTCCAATCCTGTAGC | 218793 |
rs36639275 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18634438 | GGGGACCAGAGTTCA[A/G]GACCAGCCCCTGCAA | 218793 |
rs36648201 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18689083 | CTAGTCTAGAAAAAA[A/T]GGTACCTTACAATAA | 218793 |
rs36661318 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18800624 | TCTTCCTTTGCTATG[A/C]CACCATCTTCTTCTA | 218793 |
rs36663910 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18821795 | ACTGTTAAGATGGCA[A/G]CTGGATGGAGTTTAA | 218793 |
rs36668384 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18834202 | ACTTTCTGCACAATG[C/T]TCTTCACCTTGAAAA | 218793 |
rs36670420 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ube2e2 | Mm_Celera | 14:18659391 | AAGGGGATAAAACAA[C/T]CTGTTGTTTAATTGC | 218793 |
rs36675279 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | Mm_Celera | 14:18828016 | ACAATAAGGGTAATT[A/T]AAAAAAAAATTCAGT | 218793 |
rs36676003 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Ube2e2 | Mm_Celera | 14:18666729 | TTGAATGTAAATACT[A/T]TATACAACAACATGA | 218793 |
rs36676081 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2e2 | Mm_Celera | 14:18630743 | AAAAGGGTGACAGAA[C/T]CCTGAGAGTACTGAC | 218793 |
rs36676600 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18797722 | AGCAAGGATGAGAGG[A/G]TGGCCTTCCAAAAGC | 218793 |
rs36676898 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18836174 | CTCATAGTCATCCAC[A/G]CTCTCACCGTATAAA | 218793 |
rs36679901 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18659605 | CAATAGGTTAAAGTT[A/G]ACACATATAATTCTA | 218793 |
rs36682805 | snp | G/T | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Ube2e2 | Mm_Celera | 14:18671789 | ATCTCTACCTTCACT[G/T]CCTCATCTGTAAGCT | 218793 |
rs36689071 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18886605 | CCACCTCCCTAAACA[C/T]TGTATTTCTCCACTC | 218793 |
rs36689762 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18806895 | CTGGAATCTAGATGT[C/T]CCTGCATAAGATTTT | 218793 |
rs36689904 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18755462 | TTGAAGAGTTGCTGA[C/T]ACCAGTCCCCTGAGG | 218793 |
rs36692131 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18829166 | ACCATGCTACAGTAA[C/T]ACTGCATACAGTTAT | 218793 |
rs36692748 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18698329 | CATTTCTGTTGATTG[C/T]AAAAATATCTGACAG | 218793 |
rs36693626 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18648392 | ACGAGACTGTCAAAT[C/T]GAACTGGACGTTCTG | 218793 |
rs36695879 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18829900 | TGATTCTGCAACAGT[A/G]GAACAGGAAGAACAC | 218793 |
rs36697884 | snp | A/T | 0.5 | 0 | intron-variant | Ube2e2 | Mm_Celera | 14:18629776 | TTAGAAAAAAAAAAA[A/T]ATATCTATACACACA | 218793 |
rs36698964 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18636540 | ACTGCTGGAGAATAG[A/G]AAACAGGTACCCCAG | 218793 |
rs36701372 | snp | C/G | 0.497041 | 0.0383476 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18802891 | ACTGTACACTTCCAT[C/G]GTTTCATTTTGTATT | 218793 |
rs36702575 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18756037 | AAACAAAAATAAAAC[G/T]AAGTACTCAGGTCTT | 218793 |
rs36703015 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Ube2e2 | Mm_Celera | 14:18615076 | AGTGTACACACTTAC[A/C]CTAAGTTTGGAAAAT | 218793 |
rs36703034 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18883548 | TTGCCTGTTTACCTG[A/G]CTTAACATAAAGCTG | 218793 |
rs36717805 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18836633 | AGAAGATGAGAGGAT[C/T]TTCTATAAATGCTAG | 218793 |
rs36720764 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18606974 | GCCATAGCCAGATTA[G/T]CTCTGGGCAGCTGCT | 218793 |
rs36721130 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18614296 | GATATTACAGCTGGA[C/T]TGGGCTTCTGCCCTC | 218793 |
rs36723881 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18748597 | TGCCCATGTGTCAGA[C/G]ACCATCCCATGAGAA | 218793 |
rs36726525 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ube2e2 | Mm_Celera | 14:18882238 | ATTACAATATATTTT[A/G]AACTACTGTTACCTT | 218793 |
rs36727589 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18637275 | CATTTCTGCATATGA[A/G]GCTAGAGCAAGCCAA | 218793 |
rs36728346 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18790386 | GAAGAAACTAAACTA[A/G]ACTCATACATATACA | 218793 |
rs36741978 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18664181 | TGTTAATAATGAAAA[C/T]ATAAAGTTGAAATTA | 218793 |
rs36743842 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18639330 | GTCTGCATTAGCCTC[C/T]CAACAATAAAGTGCA | 218793 |
rs36747858 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18800005 | GGTGTCATCTAAAAT[A/G]GTTCTCAGTGTAAAA | 218793 |
rs36747941 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18755633 | ATCCTTGGCAACACC[A/T]GCATAGTCCTAAAGG | 218793 |
rs36750347 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18787798 | TGCCTAAGTCACAGG[A/T]GGTCTGCTCCTTTCA | 218793 |
rs36753111 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18821055 | TTTGCTAAGTCACAG[G/T]CCTCAGATCACTGTC | 218793 |
rs36759871 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18817037 | AATGTTAGGGCTTGG[G/T]AACAGCAACCCAAAG | 218793 |
rs36762030 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18736464 | TTTAAGATAATATTA[A/G]TAGGTGATAATCAAT | 218793 |
rs36776657 | snp | C/T | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Ube2e2 | Mm_Celera | 14:18671641 | GTATGTTCAGTTGGA[C/T]CTGCTCCAGGTGACA | 218793 |
rs36777440 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18698387 | CCTTATACCACCAGG[A/G]AGGCCTTCTCCTCTC | 218793 |
rs36784895 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18838193 | ACCTATGTACTTTAA[C/T]ATCTCAGTAACTCAA | 218793 |
rs36796279 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18689592 | TCCCCTAATTTCCCT[A/C]TCTCATGGAGAAAAC | 218793 |
rs36796439 | snp | G/T | 0.46281 | 0.131194 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18721158 | GTGCTGTGAGCATGG[G/T]TCTCTCAATATGTAA | 218793 |
rs36796452 | snp | C/G/T | 0.497041 | 0.0383476 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18669512 | ACCAGCCAGCCACCC[C/G/T]ACTGAGCATCATGCA | 218793 |
rs36799611 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18835405 | AGTCAGATTGCTTTC[A/G]TTTAAGAAAATGAGG | 218793 |
rs36810231 | snp | A/T | 0.497041 | 0.0383476 | intron-variant | Ube2e2 | Mm_Celera | 14:18872168 | GGGGGTTCAGATAAT[A/T]AAAAAATATTAATAG | 218793 |
rs36812376 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18738526 | TGCAGGGGTGAGGAA[A/G]TGCTGCAGATGAGAT | 218793 |
rs36830785 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18634113 | TAGAAGCTCAAAGTA[C/T]AGTAGAATACCTAAC | 218793 |
rs36833074 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18776730 | AGAACACTGTAGTGC[C/G]TTTCTGATTTCTAAT | 218793 |
rs36833864 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18826493 | ACTAGGTATGTTTAA[C/T]ATTACAGGTACTGCC | 218793 |
rs36835940 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18788339 | GCTTAGAAGGAGGCA[A/C]TAGAGCTGCGTGTAA | 218793 |
rs36836855 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18628886 | CTCCATCTTACAATT[C/T]TTGAATATCCTTCCA | 218793 |
rs36841456 | snp | A/C | 0.21875 | 0.248039 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18772504 | GACAGACACATTGCT[A/C]GAAGCCTTCTCACCT | 218793 |
rs36846307 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | Mm_Celera | 14:18755815 | GGGCCCACCTTTGCG[C/T]TCACCACTCACTATA | 218793 |
rs36849546 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18633033 | CTTAAGGAGAGTAGA[C/T]TATAAGTTATAGTTA | 218793 |
rs36858748 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18665485 | TCAGGGGCACCTTAT[C/G]TGAAAAGCAGAAATG | 218793 |
rs36858779 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18665616 | CTTTTCAAACTCTAT[A/G]TGCTAACCAAGAATA | 218793 |
rs36858885 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18812348 | CACACACCACTGTGG[C/T]CTCAAGTGACACTGT | 218793 |
rs36861220 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18786301 | TTGTGTGTGATTGGC[C/T]CCAAGAGTTGTAGAA | 218793 |
rs36867515 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18833842 | CCACAGGCAACCTCA[C/T]ACACAGGTGGCTGTT | 218793 |
rs36879566 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18802240 | GGAATGGAGGAATCA[A/G]TCTTTACAGATTATT | 218793 |
rs36880353 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18800940 | ATTCAAAACTTGATC[A/G]GCAAAGTATATGTCA | 218793 |
rs36904429 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18689680 | CTACATAAAAAAGAG[A/T]CCTGAAGAAACCTTT | 218793 |
rs36906272 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Ube2e2 | Mm_Celera | 14:18704470 | GGCCCCTAAGCATTT[A/G]GAATGAGAGGAATGT | 218793 |
rs36906830 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18731464 | ATTAATGAATTTACG[C/T]TCAATATCACACCAT | 218793 |
rs36907891 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18819791 | CACTGGGCAGTGATC[C/T]TACACAAGAGAATGA | 218793 |
rs36914543 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2e2 | Mm_Celera | 14:18886016 | AAAGACACGCATTGA[C/T]CACAGGCTAAACAGA | 218793 |
rs36928296 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18739210 | GTAAATGTTCTATCT[C/G]TATTTTATAGAGCTC | 218793 |
rs36934208 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18639287 | TGGGTCCCTGGCTGC[C/G]AAGCAGGTTTAATCT | 218793 |
rs36937035 | snp | A/C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18614263 | GATTTTCTTCATCTT[A/C/T]GCCATCCCAAAGGTT | 218793 |
rs36939510 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18755981 | TAGGGTAGTCTGCTG[A/C]ATGGTGACCTGAACC | 218793 |
rs36942234 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18698078 | AGACTCAGCTGGGAA[G/T]GGGTTCATCATGCTG | 218793 |
rs36943503 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18812539 | AAAGAGGCCACTATG[A/G]AGAGAGATAAAGTGC | 218793 |
rs36948158 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18776522 | ACTTAATGACTTACT[G/T]TACCATTAAGATCTC | 218793 |
rs36957378 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18833191 | AACATGTAAGGAGAT[C/G]TTAATATCCCTTCTT | 218793 |
rs36957516 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18801128 | CCAGTTTATTTATGC[A/T]AAACATACTGCTGAA | 218793 |
rs36960441 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18707698 | GATGTGGTACACACC[A/G]GTAATTGTAGCACTT | 218793 |
rs36970996 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18574569 | TACCAATACCTACTT[C/T]CTGACAAGCTTCATA | 218793 |
rs36971625 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18659218 | AGCATGTATTCAGGT[A/G]CATAATGTGCTTTTT | 218793 |
rs36972428 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Ube2e2 | Mm_Celera | 14:18575325 | TAGCAAGGCAGATGC[C/T]ACAGGAATATCAGGT | 218793 |
rs36972697 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18615094 | AAGTTTGGAAAATTA[A/G]CATGTGCATTGAGCT | 218793 |
rs36978320 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18801773 | CCTAAATGTTGGGCA[C/T]TGATTCTTATTCTTT | 218793 |
rs36980918 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18814400 | TGACAGACCACCCTC[A/G]AATGGAGCTACTCAG | 218793 |
rs36989696 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18676621 | GTCAGCCAGAATGTG[A/G]AAGCTTTCATTTACG | 218793 |
rs36995113 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ube2e2 | Mm_Celera | 14:18673678 | GCTACTGTTAAAGTT[A/G]GTCCTGACTTGGCTA | 218793 |
rs36997431 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18747568 | TGTCCTCAGTCTCTC[A/G]GAGACCAGTCCACTC | 218793 |
rs37013115 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18883461 | TCCAATATGACATAA[C/T]ACCCAATTCAGTGAT | 218793 |
rs37014520 | snp | A/G | 0.489796 | 0.070696 | intron-variant, upstream-variant-2KB | Ube2e2 | GRCm38.p3 | 14:18671823 | ATATGATCAGACATT[A/G]TGATGATACCTTACG | 218793 |
rs37015315 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18747732 | AGTGAGTGATCTGAT[A/C]CCTGGGACTCAGGAG | 218793 |
rs37015878 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18810021 | TCCTGCCTATCACAC[C/T]GTCGCTTACTCAGAG | 218793 |
rs37023670 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Ube2e2 | Mm_Celera | 14:18808995 | AGTCCATCAGAAAAC[A/G]TGTTTTAAAACTTGA | 218793 |
rs37026030 | snp | A/C | 0.197531 | 0.244432 | intron-variant | Ube2e2 | Mm_Celera | 14:18774089 | TCTAACTGTCAGGTT[A/C]TGCCTCCCTTTGGAA | 218793 |
rs37033500 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18634572 | ACTCAATAGAAGCCA[C/T]TGTTTCCATCTCCCC | 218793 |
rs37038184 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2e2 | Mm_Celera | 14:18887446 | CTCTTTCAAGATCTT[C/T]CTGTCTTCTAGGGAA | 218793 |
rs37046783 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18738098 | ACATAGCAGCAGAGT[G/T]GTTAATGTGGTTGGG | 218793 |
rs37047343 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18639196 | AGACTGAGAGGTTTT[C/G]CTTTAGGTAGTGTTG | 218793 |
rs37047536 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18772357 | GCAGGACTCAGCAAG[A/G]AAACACTGGGAAGTC | 218793 |
rs37050027 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ube2e2 | Mm_Celera | 14:18643835 | TGTCTTAGGATTCAC[C/G]AAACATACCACCCTC | 218793 |
rs37059996 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Ube2e2 | GRCm38.p3 | 14:18888250 | TTCAAATGAAGTGCT[A/G]ACAACGGCTGGCTAC | 218793 |