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 |