SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3663522 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86355762 | CAAATTTATTGGGAG[C/T]ATTTTGATTCTTGCA | 70348 |
rs3668566 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86362021 | AATGAAGCTGTGTGA[C/T]TCAGTGACAGGGTGT | 70348 |
rs3669030 | snp | A/G | 0.5 | 0 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86323323 | CCAGTACTTTGAGAG[A/G]ATGAGGCAGGAGGAT | 70348 |
rs3669411 | snp | A/T | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86350172 | TATGTGGACATTTTG[A/T]AGTAGGGCAATGCTC | 70348 |
rs3669423 | snp | A/G | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86350179 | ACATTTTGAAGTAGG[A/G]CAATGCTCTTCCTTT | 70348 |
rs3670130 | snp | A/C | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86350315 | GGATGTTAGCTGATA[A/C]TGCATCGACTCTACA | 70348 |
rs3670167 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Ube2cbp | Mm_Celera | 9:86323478 | CTGAGACAACAGTAA[A/C]AATATCAGCTAAATA | 70348 |
rs3670604 | snp | C/G | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86350347 | TATTTGGGACAAATG[C/G]GACCCTGACAACATG | 70348 |
rs3670662 | snp | G/T | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86350380 | atcttctagaacaga[G/T]atctcttttgctccc | 70348 |
rs3671267 | snp | A/C | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86350475 | GCTATATTTATACTG[A/C]TGTATCCCATTTGGG | 70348 |
rs3674237 | snp | A/G | 0.5 | 0 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86327029 | CCCAGTAAGTATTCC[A/G]TGAACTGAGCTATAT | 70348 |
rs3695889 | snp | C/G | 0.359862 | 0.224567 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86328178 | AGAAGCATTGCCCTC[C/G]AAAGCCTCATCTCAG | 70348 |
rs3706545 | snp | A/G | 0.5 | 0 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86453517 | GAGACAAGGTCTCAA[A/G]TGTCCCGGTCCAGAC | 70348 |
rs3706588 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86453536 | CCCGGTCCAGACTCA[A/C]ACTCAGCTATGTAAT | 70348 |
rs3706640 | snp | C/T | 0.5 | 0 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86453562 | GTAATGGAGGATGAC[C/T]GGGAACTCCTGGTGC | 70348 |
rs3706675 | snp | G/T | 0.5 | 0 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86453587 | TGGTGCTCTTGCTTC[G/T]AAATCCCAAGTGTTA | 70348 |
rs3708292 | snp | A/T | 0.290657 | 0.246672 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86453803 | GAGAATGTCCTGTGT[A/T]GAGACTCCACTTTCA | 70348 |
rs3720276 | snp | A/G/T | 0.48 | 0.0979796 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86312565 | TAAAAATCTACTGCC[A/G/T]CAAGCACAAATTGTA | 70348 |
rs3720863 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86355436 | TTTCCCCCTGGTGAC[C/T]AACAGCTATTTCAGA | 70348 |
rs4139166 | snp | A/G | 0.5 | 0 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86367386 | CTTGGGGGGGGGGGG[A/G]AGCCTAAATTATAAA | 70348 |
rs6204918 | snp | C/T | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86421227 | attcaatcgccagga[C/T]atatggaggaagaga | 70348 |
rs6204955 | snp | A/G/T | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86421254 | gagaactgactccca[A/G/T]aggttgcctctgatt | 70348 |
rs6205011 | snp | C/G | 0.359862 | 0.224567 | intron-variant | Ube2cbp | Mm_Celera | 9:86421293 | TGCACTGTGGCATAA[C/G]GACGATCTATTGAGC | 70348 |
rs6244612 | snp | C/T | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86347423 | AACCCTAGAGTCAAA[C/T]ATCTCATAATTAACA | 70348 |
rs6307522 | snp | G/T | 0.5 | 0 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86432947 | tttttctggagtcca[G/T]cttcatgagttcttt | 70348 |
rs6307593 | snp | C/T | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86432990 | tattagtcccctatc[C/T]gatttnggataggta | 70348 |
rs6307598 | snp | A/G | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86432996 | tcccctatcngattt[A/G]ggataggtaaagatc | 70348 |
rs6308611 | snp | A/G | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86433172 | gagtgtggacacttc[A/G]ccccttcttagaatt | 70348 |
rs6317340 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ube2cbp | Mm_Celera | 9:86318401 | TATTACCTTACAAAA[C/T]GTCTAGGAAAACAGG | 70348 |
rs6317843 | snp | C/T | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86318486 | TATACCTTAAAAAGT[C/T]TTTTAAAAAAGATTT | 70348 |
rs6318279 | snp | A/G | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86318551 | catatatatatacat[A/G]tatataatacagata | 70348 |
rs13464046 | snp | A/C | 0.33241 | 0.236027 | synonymous-codon, intron-variant | Ube2cbp | GRCm38.p3 | 9:86451929 | CCCTGACGGCTGCAC[A/C]GAGATCCGACTTCCA | 70348 |
rs13480318 | snp | C/T | 0.492188 | 0.0620098 | utr-variant-3-prime | Ube2cbp | Mm_Celera | 9:86307594 | TTGAATATTCCTCTC[C/T]GTGGGAAGTAGAGGT | 70348 |
rs29586276 | snp | A/C/T | 0.48 | 0.0979796 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86310175 | AGAGGTTTTTTTTTT[A/C/T]TCTCTCTCTAGTTTT | 70348 |
rs29587241 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86345241 | GCAGTTCTATCTTTT[C/T]CATGTTGTTAACAAC | 70348 |
rs29589345 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86391533 | TGCCACCCCTTGGCT[A/G]GTGGTCCTGGGTTCT | 70348 |
rs29589697 | snp | A/G | 0.5 | 0 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86411311 | GGTACTGGAGGGATG[A/G]CTCAGTGGTTGACCA | 70348 |
rs29590803 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86372199 | AGATAATGCCTGACT[G/T]CTGAGGCTTCACGTG | 70348 |
rs29591130 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Ube2cbp | Mm_Celera | 9:86422037 | TTAAAACATAGCACT[A/G]ATTCTAAAAACTGTC | 70348 |
rs29592405 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86444680 | ATTCTAGTCTGACAT[A/G]AATCTATTTCTAGGA | 70348 |
rs29593657 | snp | G/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86358545 | CTTATTGGTGGGGTT[G/T]AAAAACAGTAAGTAG | 70348 |
rs29595903 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube2cbp | Mm_Celera | 9:86309555 | GGGAGAGGCAGGGAT[A/G]TTGCAGAGCATCCTA | 70348 |
rs29635005 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Ube2cbp, Dopey1 | Mm_Celera | 9:86466257 | TTGGGCTATGTGAGT[A/G]CAGGGCCATCTAGAG | 70348 |
rs29637252 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Ube2cbp | Mm_Celera | 9:86309623 | GCAGTGAAGAGAAAC[A/G]CTGTAATTACAGGAT | 70348 |
rs29640027 | snp | G/T | 0.32 | 0.24 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86448649 | ACCACGGTGAGAGTC[G/T]GGCTTCACTTTGTTC | 70348 |
rs29640879 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Ube2cbp | Mm_Celera | 9:86336672 | ACTCAAAATAGTAGC[C/T]GCTGCCTCTTTTCCC | 70348 |
rs29646044 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86330858 | CACACACCCAGCAGT[C/T]CCTTTAATTAATGTG | 70348 |
rs29647156 | snp | C/T | 0.5 | 0 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86420605 | CAGAAAAATGAAAAA[C/T]AAACCAGCAGCTGGC | 70348 |
rs29647630 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86463927 | TCTCTTAGTAGGATA[A/G]GGGACTGAGCTGTGT | 70348 |
rs29648686 | snp | A/C/T | 0.554688 | 0.10335 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86360533 | TGCACCAGGACGAGA[A/C/T]CTATCGGAGCGAGGG | 70348 |
rs29650929 | snp | A/G | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86420711 | AAGCCAGGAAGGCAG[A/G]ACAGAGAGGTAGGCC | 70348 |
rs29684096 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86390176 | TTTATTTATTTCTCT[A/G]TCTTCTTGTACATTG | 70348 |
rs29687199 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Ube2cbp | Mm_Celera | 9:86314359 | GATAATAGGGATGAC[A/G]GAAGGCATCAGGTAG | 70348 |
rs29687399 | snp | G/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86455067 | ATGTGTATGAGTGTG[G/T]GTGGGCATGTGGGTG | 70348 |
rs29688043 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86333359 | CCCCCCACCCCACTT[C/T]CCTTTGATCTGACAA | 70348 |
rs29688064 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86434501 | GTGGAAGGAATGACC[C/T]AGCTCCACAGCATTC | 70348 |
rs29688727 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Ube2cbp | Mm_Celera | 9:86354275 | TCAATTTATATGTCA[A/C]CTTTTGCCTAGTTCA | 70348 |
rs29688943 | snp | A/G | 0.5 | 0 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86438507 | ACACTGTGGGAATGT[A/G]GGAATGCTACAGAGC | 70348 |
rs29689335 | snp | C/T | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86457780 | GTTCTCAACATTGTA[C/T]GTCACCAGGGAAATT | 70348 |
rs29690505 | snp | A/C | 0.35503 | 0.226867 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86435254 | AAGTAGGAGGGCAGT[A/C]ATTTCAGCCTTGTGT | 70348 |
rs29691475 | snp | C/G | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86442172 | AAGATAATAAACCTG[C/G]GGTTCCACGGGCAAT | 70348 |
rs29691712 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86405036 | TAGTCCTGGCTGCCC[A/T]GGAACTCACTATGCA | 70348 |
rs29693434 | snp | A/T | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86420466 | TCAGCATTCAGGAGG[A/T]ATAGGCGAGGACCTG | 70348 |
rs29694243 | snp | A/G | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86388569 | AAAGCTGGAAGAGTC[A/G]AGAGAATTGCCTAGT | 70348 |
rs29701202 | snp | A/G/T | 0.336735 | 0.234472 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86405571 | AAACTGGAATTAGAA[A/G/T]GGAAAATAGCCTAGA | 70348 |
rs29728759 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86393215 | AGAGAGGACACAGCC[C/T]GTTGTGGGTGGTGCC | 70348 |
rs29733051 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86343976 | GGGCATTCGATCAAA[A/T]TAGACATTTTGCAAA | 70348 |
rs29735993 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86449312 | CTCGGTAGAGTGTCC[C/T]CACCCAAGAGCAAAA | 70348 |
rs29737332 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86449038 | TCCAAAAACAAAAGA[C/G]ATTTTGCTTAGAATT | 70348 |
rs29737864 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Ube2cbp | Mm_Celera | 9:86311145 | GCATGTATATCTGTG[C/T]CTGGTATCTGCAGAG | 70348 |
rs29737908 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Ube2cbp | Mm_Celera | 9:86430680 | AGCACTGAAGAATAA[C/T]TTTTACTGGATTGAG | 70348 |
rs29738214 | snp | G/T | 0.5 | 0 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86372966 | TGATGGGTGAGACCA[G/T]CTGGGAGGGGTGGAG | 70348 |
rs29738485 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Ube2cbp | Mm_Celera | 9:86452290 | CAAGATTGTCATAAA[A/G]AGTCACAGATGCCAG | 70348 |
rs29740373 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86463550 | GGATCTTTTGAGCTG[A/G]GAAGAGCCACCTCAA | 70348 |
rs29740730 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86353500 | TTTCATAGTGTTACC[A/G]TACAGTGGTTTGACT | 70348 |
rs29741960 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86367748 | TAAAGTGGGAGCAGA[G/T]ACAGGTGGGATTTTA | 70348 |
rs29742852 | snp | C/T | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86310061 | TGGTTTCCCATGCTT[C/T]TAACATGGAGAATGA | 70348 |
rs29744346 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86430528 | TTTTCTCCTTCCTGC[A/G]TGCTATCCTAGACCC | 70348 |
rs29744677 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86400560 | GATGCAGGGATGGTT[C/T]AATATACAGAAATCC | 70348 |
rs29744993 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86411796 | CCTGGGGACATGAGC[A/G]CTGGAGAGCTGACTC | 70348 |
rs29745554 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86410694 | CCTGTAGAGAACAAA[C/T]GCAGCTGTGAATACA | 70348 |
rs29746306 | snp | A/G | 0.49827 | 0.0293608 | utr-variant-3-prime, downstream-variant-500B | Ube2cbp | Mm_Celera | 9:86307267 | ATTTATTAATTTGCA[A/G]TAGCATGTGGTGAAG | 70348 |
rs29747429 | snp | A/T | 0.498615 | 0.0262793 | intron-variant | Ube2cbp | Mm_Celera | 9:86312959 | GTGAGTGCTGAGGAC[A/T]CAGAGCTGGGATGTC | 70348 |
rs29751530 | snp | G/T | 0.265928 | 0.249492 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86338474 | AGACCCATGATGACT[G/T]TAATTAAAAACAAGT | 70348 |
rs29787756 | snp | A/C | 0.484429 | 0.0868505 | intron-variant | Ube2cbp | Mm_Celera | 9:86358890 | AGGAATAGAGAGATG[A/C]TTTACCATCAGAGGA | 70348 |
rs29789770 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86355182 | GTTTCTTTGAATGCT[G/T]CATGTCTCCACCTCT | 70348 |
rs29790314 | snp | G/T | 0.304688 | 0.243945 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86327493 | TTGTTCTTGTGCCCT[G/T]GAGTGTCACAGCCTT | 70348 |
rs29790911 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86358594 | GAGGAGTTATCCTGA[A/G]ATGTAACTATCTGTG | 70348 |
rs29793476 | snp | A/G | 0.473373 | 0.11227 | synonymous-codon | Ube2cbp | Mm_Celera | 9:86372403 | TCCTGGATAGTATTA[A/G]CAGCAGCTCCAAACA | 70348 |
rs29794459 | snp | A/T | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86410906 | CCTGTCTCAAAAAAA[A/T]ATATATATATGCATA | 70348 |
rs29795067 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86426677 | CTGACATAAAACTAA[C/T]CAGCACAGCTATCAA | 70348 |
rs29795270 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86442135 | ACTTTAGAGAACAGG[C/T]AACATCTGAGTTGGC | 70348 |
rs29799880 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86411759 | GCCCCACCCATCATC[C/T]GGGCATCATGGGAGA | 70348 |
rs29826781 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86310080 | CATGGAGAATGAGAA[C/G]TTAAACTGACCAAAT | 70348 |
rs29829734 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86427480 | TTCTCAACACACTGA[C/T]ATCATAGACATACTT | 70348 |
rs29830877 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Ube2cbp | Mm_Celera | 9:86311634 | CTGCTGCTGAATATA[A/G]TATGACCTATTCCTC | 70348 |
rs29833855 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86450312 | TTTTGTCCACGGTTA[A/G]AATATTAAATGTTGC | 70348 |
rs29837783 | snp | A/T | 0.290657 | 0.246672 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86337107 | AAGCTGAAAAAAAAA[A/T]GCCCTGTAAAGAAAG | 70348 |
rs29838295 | snp | A/G | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86421383 | ATGGAAATGGGCAAG[A/G]CAGAAAACTCTAGGT | 70348 |
rs29838656 | snp | G/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86336764 | ACATTACAATATATT[G/T]AAAACTAGATTTCTT | 70348 |
rs29839819 | snp | A/T | 0.32 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86463875 | TTCGAGAAACAGGGA[A/T]ATTGTGTAGATTGGT | 70348 |
rs29842833 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86333344 | AAATGTTTCTCCCCC[C/G]CCCCACCCCACTTCC | 70348 |
rs29872870 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86422743 | ATGTGACTCCTAACA[A/G]CATCAAGTAGCATTT | 70348 |
rs29879488 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86429984 | ACTCAGCAGAGGCAA[A/G]GACTAAGGTGTCTGA | 70348 |
rs29881321 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86311091 | TTAATTTCAATTTTT[A/T]AATTAAACAAATTTT | 70348 |
rs29885343 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Ube2cbp | Mm_Celera | 9:86327804 | AGTTGGATTTCATAA[A/G]CATTTCTCCTTGGGG | 70348 |
rs29886563 | snp | A/C | 0.444444 | 0.157135 | upstream-variant-2KB, utr-variant-5-prime | Ube2cbp | Mm_Celera | 9:86464945 | GGGATCCGGCGGCGG[A/C]CGTCTGTCGGCTAGA | 70348 |
rs29887124 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86400504 | CTGAATCCAAGAATA[C/T]ATCAAAATCATCAAT | 70348 |
rs29888135 | snp | A/C | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86372653 | TGGTGGGTAAAGGAG[A/C]TTTTTGCCACGTCTG | 70348 |
rs29888624 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86311071 | AAAAACAAAAATTTT[A/T]AAAATTAATTTCAAT | 70348 |
rs29889554 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86434345 | ATTTCATTGTTATAG[A/T]TTAAAGTAGTATAAG | 70348 |
rs29890912 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Ube2cbp | Mm_Celera | 9:86360378 | GCCACATTTCTTTTA[C/T]GAATACGACTCCTGG | 70348 |
rs29891075 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86407858 | TGCCAGGTATACAGC[C/T]TCGGGAGGCGGAAGT | 70348 |
rs29892001 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86405957 | GCTACGCGGCGGCAA[A/G]CACAATTCCCCATCA | 70348 |
rs29894939 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86434570 | AATAATAAATAAAAA[A/T]AAACAAACAAACAAG | 70348 |
rs29895187 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86315009 | ACCTTCCCACTAACA[A/G]TGCACAAGCATCTAA | 70348 |
rs29897117 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86346190 | TTATTATCCTTTAAG[C/T]TTCTAATGATCACTC | 70348 |
rs29913269 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Ube2cbp | Mm_Celera | 9:86360354 | TAGGTGAAGGCCAAG[C/T]CTCTGGAAGCCACAT | 70348 |
rs29915139 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86378030 | CAAGGGACCACAACT[A/G]GGTAAGGGGCCACAA | 70348 |
rs29923100 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86361223 | CATCTGAGAAGTGTC[A/G]TCTGCTACTTCCACT | 70348 |
rs29924265 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Ube2cbp, Dopey1 | GRCm38.p3 | 9:86466381 | TTTTAAAGTTTATCA[C/T]GTTGCTACATAAATT | 70348 |
rs29930617 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ube2cbp | Mm_Celera | 9:86419428 | AAGAAGGGAAGGCAC[A/G]AAAAAAAAATTCTTC | 70348 |
rs29932987 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86435085 | CCCACAGCTTCTCAA[A/T]GCTAACTAGCACTTG | 70348 |
rs29933546 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86371939 | TGGGGGTTGCATACA[A/T]ATATCCTGAATTGAT | 70348 |
rs29934048 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86388012 | AAAGCCCTTACCCTG[A/C]ATACACAGAGATTCC | 70348 |
rs29936675 | snp | C/T | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86353917 | TCACTTAGTGAACTA[C/T]GGATTATTTAAATTT | 70348 |
rs29937725 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Ube2cbp | Mm_Celera | 9:86443835 | TATGTTTTCCTCTAA[C/G]ACCTAAACTTCTGTG | 70348 |
rs29938016 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86410716 | GTGAATACACACTCA[C/T]GTCTACCACTATTCT | 70348 |
rs29941056 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86430420 | GAAATCAAAGCAAAC[A/G]TTACAGAGAACTGGC | 70348 |
rs29942474 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86422665 | AGGAAAAGCAAGTTC[A/T]CTACATATTGGTGGG | 70348 |
rs29943315 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86396160 | AAATAGCTTTAGCCA[A/G]GGAATTTTATCACAA | 70348 |
rs29944014 | snp | A/T | 0.32 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86392061 | TTCTACTGGAACAAC[A/T]GATGTTGGTCAGCTG | 70348 |
rs29944209 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Ube2cbp | Mm_Celera | 9:86339503 | AACTGACCAGGTAGA[A/G]ATCGGTTGAGGAAAA | 70348 |
rs29945540 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86371434 | GCGACAGAGAAACAC[C/T]AAGTCACACTTTCTG | 70348 |
rs29946119 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86354145 | CAATAGAACATTTAT[A/T]CAGTAGTAAGCAATG | 70348 |
rs29946573 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86391351 | TAACCCTTGAGGTAA[A/T]GTGCTGGCTAGTTTT | 70348 |
rs29967921 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Ube2cbp, Dopey1 | Mm_Celera | 9:86465315 | TCCAAAAATATCCAC[A/G]ATTGATTGGCCATTA | 70348 |
rs29984145 | snp | A/T | 0.401235 | 0.199068 | intron-variant | Ube2cbp | Mm_Celera | 9:86335877 | TTTAATATGACGGTT[A/T]AACTAGGAAATGTAT | 70348 |
rs29986077 | snp | G/T | 0.495868 | 0.0452663 | intron-variant | Ube2cbp | Mm_Celera | 9:86310872 | ATCTTAGTCAAGAAA[G/T]CTATATTGTTGACAG | 70348 |
rs29986712 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Ube2cbp, Dopey1 | GRCm38.p3 | 9:86466389 | TTTATCACGTTGCTA[C/T]ATAAATTCCTGTTTC | 70348 |
rs29988337 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2cbp | Mm_Celera | 9:86312733 | GGTTCATTGAGTAAG[C/T]ATACAGTGGCACCAG | 70348 |
rs30012083 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86412081 | TAGAACTGACCCTGA[C/T]GGCAGGGGAGAAAGT | 70348 |
rs30029763 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86316283 | GCTGTTTTCCTTCAT[C/T]TATCTGCCCCTCTAG | 70348 |
rs30029796 | snp | A/C | 0.5 | 0 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86404028 | ACCCTGTCTCAAAAA[A/C]ACCAAACAACAACAA | 70348 |
rs30029948 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Ube2cbp | Mm_Celera | 9:86313307 | GTCAGGCAGGACAGG[C/T]GACTCCAGTGATCTG | 70348 |
rs30030418 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86371188 | TCCTGCAGAAGGAGA[A/G]AGTGTGATTTAAGGT | 70348 |
rs30030892 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86419112 | CACTCCTTCAAGTTG[C/T]AAAAACCAAGCCTGT | 70348 |
rs30030893 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86412129 | TGTAAGCATGTAAGA[C/G]TTGGCCCCACAACTT | 70348 |
rs30033370 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86359006 | CACTGAAGAAGGTAC[A/T]GGATCCATACCCCAG | 70348 |
rs30033557 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2cbp | Mm_Celera | 9:86437764 | ATGAAACATGCATTG[C/T]GATTATAATGATCCA | 70348 |
rs30033988 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86394083 | TTCTGATATGAATCT[C/G]AGAAACAGCCACTTG | 70348 |
rs30035182 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86426516 | AACCCAGGAGCACCA[A/G]CTAAGGGATGGTACC | 70348 |
rs30035196 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86455252 | TGAAAAAATAAAGTT[A/G]GTCCATATACACAAT | 70348 |
rs30036122 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Ube2cbp | Mm_Celera | 9:86353943 | AATTTGTTGCTTTTC[C/T]GGTACTTGTTTTAAT | 70348 |
rs30036742 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Ube2cbp, Dopey1 | GRCm38.p3 | 9:86465768 | CCACTGTTCATCATT[A/G]AGGGATGTCAGGACA | 70348 |
rs30039463 | snp | A/T | 0.456747 | 0.140554 | intron-variant | Ube2cbp | Mm_Celera | 9:86327538 | TCTCTGCACCACTGA[A/T]CACACAGCTGGAGGC | 70348 |
rs30039876 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86391292 | CTGTTCAAATAATCC[C/T]AGGCTCTATTCAGTG | 70348 |
rs30039878 | snp | C/T | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86420725 | GGACAGAGAGGTAGG[C/T]CTGGCTACAAGAGGG | 70348 |
rs30039994 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86343071 | ATGCAAAAAAAAAAA[A/C]CAATAACATTGCCAC | 70348 |
rs30040785 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86353964 | TTGTTTTAATCTTTA[C/T]GCCATTTGGAGCTTA | 70348 |
rs30042363 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Ube2cbp | Mm_Celera | 9:86361041 | AGTCTTCTAAAGAAA[A/G]TACAAACACAAAAAC | 70348 |
rs30080080 | snp | A/C | 0.487535 | 0.077957 | intron-variant | Ube2cbp | Mm_Celera | 9:86310139 | ACCACCAAGTAAGGA[A/C]AATCTGAAATTTTGA | 70348 |
rs30084087 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | Ube2cbp | Mm_Celera | 9:86312555 | AAGCGTTTCATAAAA[A/C]TCTACTGCCACAAGC | 70348 |
rs30084484 | snp | A/G | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86421609 | AAATATCCACCCATG[A/G]GAAAAAAAAAAATGG | 70348 |
rs30085231 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Ube2cbp | Mm_Celera | 9:86372630 | AAAGATATAAACAAG[A/G]TATGGCTTGGTGGGT | 70348 |
rs30085305 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86387301 | TATGGAAGAGTTGGA[A/G]GAAGCACTGAAGGCC | 70348 |
rs30085992 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Ube2cbp | Mm_Celera | 9:86339255 | CACACCAACATCAAA[A/T]ATCAGCAAATATTAA | 70348 |
rs30088079 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86444316 | GGTGGGCAGGATGAC[A/G]GGGATTGCACATGAG | 70348 |
rs30089809 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86412190 | AGATGGCTTTCTCCC[C/T]TTCTTCATGCCTTAC | 70348 |
rs30093281 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86344861 | TTAGTCCTTGCCAAC[A/C]AGGATAGTAACGCTT | 70348 |
rs30114103 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86408160 | CGTAAGTGTATCTTA[A/G]TGAAGAAGAGAAGAG | 70348 |
rs30120186 | snp | C/T | 0.493827 | 0.0552116 | utr-variant-3-prime, downstream-variant-500B | Ube2cbp | Mm_Celera | 9:86307244 | ATATTAAGACACCAG[C/T]GTTGTACATTTATTA | 70348 |
rs30120676 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86405002 | GTTTTGTTTTGTTTT[C/G]ACACAGGGTCTCATT | 70348 |
rs30121891 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Ube2cbp | Mm_Celera | 9:86390803 | TTCTAATCAAACCAC[A/G]CGAATGGCCAACCAG | 70348 |
rs30122345 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86367743 | CCAACTAAAGTGGGA[A/G]CAGAGACAGGTGGGA | 70348 |
rs30124764 | snp | C/T | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86360490 | AGCCCAGACCAGCTC[C/T]CACCTCCACTCCAGT | 70348 |
rs30126419 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2cbp | Mm_Celera | 9:86313112 | GCAAAACTTCCCCCT[A/G]GAAAAAGCTTTTAAG | 70348 |
rs30126997 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Ube2cbp, Dopey1 | GRCm38.p3 | 9:86465853 | GGGTGAGTTTACTGG[C/T]TTGCTCCCATGGTTT | 70348 |
rs30128454 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86410502 | GGTATGGTAATAACA[C/T]CAGCTTAATAAAATA | 70348 |
rs30130802 | snp | A/C | 0.484429 | 0.0868505 | intron-variant | Ube2cbp | Mm_Celera | 9:86314894 | GCTATTGTCTATTTG[A/C]TGACTTAATGTCCTC | 70348 |
rs30132376 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86419678 | AGAGTTTACAGTTTG[C/T]TCCGTTATGCCCTGC | 70348 |
rs30133274 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86451138 | GTACTGTTCCATCTA[A/G]AATGGTCTCTTCATA | 70348 |
rs30134184 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86336347 | GTTGACATACTTATC[A/G]TTTTAATATGGTAAT | 70348 |
rs30135461 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86388195 | AAGAGTCAGACAGCA[A/G]GCTATGGATAATATT | 70348 |
rs30136252 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86371768 | AATAAATACCCAGGG[C/T]GGGGAGAAGGGCTGA | 70348 |
rs30138187 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Ube2cbp | Mm_Celera | 9:86313092 | CCAATCGACATGCAA[A/G]CAAGGCAAAACTTCC | 70348 |
rs30140132 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86391283 | ATATTCATTCTGTTC[A/G]AATAATCCTAGGCTC | 70348 |
rs30141099 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86443896 | GTTTGCTACTTATTT[C/T]TGATGCACTTGAAAC | 70348 |
rs30176114 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube2cbp | Mm_Celera | 9:86314420 | TGGCATTGTCAAACA[A/G]GAGGAATCAATAAAA | 70348 |
rs30177357 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Ube2cbp | Mm_Celera | 9:86340784 | TTATATTGCTAATTA[C/T]ACAAGCCAATTCAAA | 70348 |
rs30179739 | snp | C/T | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86354586 | ATTTATTGGCATGCT[C/T]GCCATGCTTAATCAC | 70348 |
rs30180718 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Ube2cbp | Mm_Celera | 9:86311775 | AGACAGGAGTAGGGG[C/T]CAGCTAAGCAATGAG | 70348 |
rs30181651 | snp | C/G | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86398825 | GGAAAGAGATGAGGA[C/G]ACATAGAGGTAAACA | 70348 |
rs30183033 | snp | A/G | 0.42 | 0.183303 | intron-variant | Ube2cbp | Mm_Celera | 9:86355366 | TCCATGAAGCCTGGA[A/G]GTGGAGTTGTCATGG | 70348 |
rs30183774 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86315427 | TTCTGGACAGTAACT[A/G]TCAAATGAACAGTGG | 70348 |
rs30184359 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86368075 | CCCCCACTAGCCAGG[A/G]CACACTGAAGCACAG | 70348 |
rs30186017 | snp | A/C | 0.33241 | 0.236027 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86336860 | GAAGAAATCTCATGT[A/C]GAAGACTAAAAGTCA | 70348 |
rs30186469 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86426547 | ACCCACACCCGATAG[C/T]CTAGGCCCTCCTCCA | 70348 |
rs30209512 | snp | C/G | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86398820 | ACCTAGGAAAGAGAT[C/G]AGGAGACATAGAGGT | 70348 |
rs30209518 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Ube2cbp | Mm_Celera | 9:86314515 | TAAACTTAAAGTAGG[A/G]AAAAAATCAATTAAA | 70348 |
rs30227505 | snp | C/T | 0.5 | 0 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86316291 | CCTTCATTTATCTGC[C/T]CCTCTAGCACCTTTA | 70348 |
rs30227917 | snp | A/C | 0.49827 | 0.0293608 | intron-variant | Ube2cbp | Mm_Celera | 9:86311342 | AATAATTAGTTATAG[A/C]TATACACAGTTGTCC | 70348 |
rs30227921 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86426249 | AATTTGCTTTCTGGT[A/G]ATGTGATAAACACCA | 70348 |
rs30228269 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86361296 | CAGACAATACCCTCA[C/T]GTCATCACCTTGGGG | 70348 |
rs30228510 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86452039 | TAAAAGCCAAGTGAA[C/T]GACTTCTCTCTGATG | 70348 |
rs30230397 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86457368 | TTATTAAGATTAAAA[A/T]TTTTGCTCATCAAAA | 70348 |
rs30230654 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Ube2cbp | Mm_Celera | 9:86358373 | TAAGCTCGCAACCTG[A/G]AAATTCCAAAACATG | 70348 |
rs30231226 | snp | A/C | 0.456747 | 0.140554 | intron-variant | Ube2cbp | Mm_Celera | 9:86434098 | TCAGGAGTATCTCCA[A/C]GGCGCATGCTCCCTT | 70348 |
rs30233160 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86422017 | GATCTGTGCTGCTTG[G/T]ACAATTAAAACATAG | 70348 |
rs30234080 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86444687 | TCTGACATGAATCTA[C/T]TTCTAGGAGGTCTAA | 70348 |
rs30239607 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86377954 | TACAGATGTCAGAAA[C/T]GCAGCTGAAAAACTA | 70348 |
rs30256536 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86335928 | AAAACACTACTTTCA[C/T]AGACAGAAGTATCTA | 70348 |
rs30273934 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86412252 | AGTTATGAGAGTGGG[A/C]GAACTGGTCATGTCC | 70348 |
rs30275859 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Ube2cbp | Mm_Celera | 9:86311754 | AAAGATGCTTTCATC[A/G]TGCTAAGACAGGAGT | 70348 |
rs30277514 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Ube2cbp | Mm_Celera | 9:86313389 | GTCTCGGTTAATTTT[A/T]TGTCATATTTCAGCA | 70348 |
rs30281530 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Ube2cbp | Mm_Celera | 9:86390693 | TCGGTGAAAGCTTGG[C/T]CTTTACTGAAAGAAA | 70348 |
rs30284108 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86419269 | ATAGGAGCTAAGCTC[C/T]GATACGCAAGCTAAA | 70348 |
rs30287415 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86353670 | GTGCCCTTTTCTGGC[C/T]TCCACAGACACAACG | 70348 |
rs30288356 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86367721 | CATAATTTAAGAAAG[A/G]CAAAACCCAACTAAA | 70348 |
rs30288980 | snp | A/C | 0.32 | 0.24 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86464005 | AAAGTAGGTTTCTCA[A/C]AGAGTTTGTTTGGTA | 70348 |
rs30323958 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86392165 | AGAGTCACCGGGACA[C/T]AGACGCTATGTTCCA | 70348 |
rs30326909 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86426853 | CCACACCAATCATCA[A/G]TCAAGACAATGTTCT | 70348 |
rs30327292 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Ube2cbp | Mm_Celera | 9:86337199 | GAAGCAACTATGATG[A/G]CCTAATTACAACCCC | 70348 |
rs30328126 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86450306 | GATTTATTTTGTCCA[C/T]GGTTAAAATATTAAA | 70348 |
rs30328559 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86408247 | AGAGGAAGAAGAAGA[A/G]GAAGAGGAGAGGAAA | 70348 |
rs30328569 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Ube2cbp | Mm_Celera | 9:86312427 | CTGGACAGACCTACT[A/G]TGACACTGGAGTGAA | 70348 |
rs30328838 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86387358 | ACAAATACAGTCAAC[C/T]AACCAGAACTCTGGG | 70348 |
rs30329214 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86400442 | AACTTCAGACGAATC[A/T]CTCTTACTAACATTG | 70348 |
rs30330674 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86349266 | CTGTCTGGATTTGAG[A/G]CTTTACCCATATTTA | 70348 |
rs30330983 | snp | A/T | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86335936 | ACTTTCATAGACAGA[A/T]GTATCTAGTAACACT | 70348 |
rs30331135 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86422216 | ATCCTCAGACTTAGG[C/T]TTCTGCTTCACTTTC | 70348 |
rs30332012 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86410375 | CCAGCAAAGAGAAAG[A/G]AAAAGTCAACAAAGT | 70348 |
rs30332516 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Ube2cbp | Mm_Celera | 9:86335482 | TTTACAAGCGAGAAA[A/G]ATGTTGGTGTCAGAC | 70348 |
rs30332893 | snp | A/C | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86310111 | AATGCAAAGCCCCCA[A/C]CCCCACCCCCACACC | 70348 |
rs30333182 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86355194 | GCTTCATGTCTCCAC[A/C]TCTCTAAATGATGTG | 70348 |
rs30333200 | snp | A/G | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86420849 | agaaagaaagagaga[A/G]agagagagagagaga | 70348 |
rs30333220 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86426447 | AAGTCAGGAGCTGAT[A/G]CAAAGGCCATGGAGG | 70348 |
rs30334925 | snp | C/T | 0.255 | 0.24995 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86451524 | TTATGGTTAAAGAAA[C/T]GAACTGGGCAGTTTG | 70348 |
rs30340701 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Ube2cbp | Mm_Celera | 9:86307496 | CATTCAGCTCCCCAG[C/T]GAAGTTCCTCGCTGC | 70348 |
rs30374212 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86388167 | TCTCTAAGCTAGTGA[A/G]TGACCCTGTCTCAAG | 70348 |
rs30375203 | snp | A/T | 0.46281 | 0.131194 | intron-variant | Ube2cbp | Mm_Celera | 9:86450212 | GTTCCCTTTTCAGGT[A/T]TTTGAACAAAATGTT | 70348 |
rs30375945 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86419259 | TAAATAGTACATAGG[A/C]GCTAAGCTCTGATAC | 70348 |
rs30379620 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon | Ube2cbp | Mm_Celera | 9:86440619 | CAAATTCACTAAGAA[A/G]AAAGAGTCCCCAATA | 70348 |
rs30382101 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Ube2cbp | Mm_Celera | 9:86388719 | CATCTTACAACTGGG[A/G]CTTACTCATTACCTG | 70348 |
rs30382921 | snp | C/T | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86421682 | GACATGGAAGACCTT[C/T]CTATGAAAGGGTTTT | 70348 |
rs30387503 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Ube2cbp | Mm_Celera | 9:86370685 | ATTATTCTCAGTTTA[G/T]ATCATACATGAAAGA | 70348 |
rs30387907 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86387447 | GACACATATGTAGCA[C/G]ATGTGCAGTTTTGTC | 70348 |
rs30389245 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86392173 | CGGGACATAGACGCT[A/G]TGTTCCAGAGGCAAC | 70348 |
rs30419821 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86312648 | TAAAACAGGGATACC[C/T]CAGTAAGTATATTAT | 70348 |
rs30424394 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86455422 | TTTTTATATATGTGG[A/G]TGAAGGTGGGTTTAG | 70348 |
rs30424673 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86309892 | AAATAAATGGCTTAC[C/T]GAGCACACAAGGCCT | 70348 |
rs30424943 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Ube2cbp | Mm_Celera | 9:86420419 | CTAATCAAAAGAAAA[A/C]TGAGCTGGGTGTGGT | 70348 |
rs30425006 | snp | A/C | 0.5 | 0 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86339069 | GTTGTGTGACTCTGC[A/C]AAGAGCCACAAAGAA | 70348 |
rs30425454 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86340093 | AGGTGCTTAAGGCTG[A/G]CTGCAAAGAAAAAAA | 70348 |
rs30430917 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86444704 | TCTAGGAGGTCTAAC[A/G]AAATCCAAACACAAT | 70348 |
rs30434476 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86360550 | TATCGGAGCGAGGGA[C/T]GAGAGGACAATACGA | 70348 |
rs30437688 | snp | A/C | 0.415225 | 0.187619 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86452091 | CAAACCTTAACCCAG[A/C]ATAGAGACCCTAAAA | 70348 |
rs30437974 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Ube2cbp | Mm_Celera | 9:86313408 | CATATTTCAGCAGCT[C/T]TGCTTCTGTGATCTG | 70348 |
rs30438270 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Ube2cbp | Mm_Celera | 9:86327675 | CTATGAGAATTTTTG[A/G]GTTGCAAAGTTAAAA | 70348 |
rs30442721 | snp | A/C | 0.387812 | 0.208586 | intron-variant | Ube2cbp | Mm_Celera | 9:86333565 | ATGTTGTTTGTGTTG[A/C]ATTAACTTTGAGCTA | 70348 |
rs30449944 | snp | G/T | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86421369 | GTCCTGATAAAATTA[G/T]GGAAATGGGCAAGAC | 70348 |
rs30454338 | snp | A/G | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86420599 | ATCAAACAGAAAAAT[A/G]AAAAACAAACCAGCA | 70348 |
rs30473867 | snp | A/G/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86422639 | TTGTAATAAAAAGGC[A/G/T]AATTATTTACAGGAA | 70348 |
rs30474863 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86454968 | TGTAAGTGTGTGTGT[A/G]AATGTTTGTGTATGT | 70348 |
rs30475795 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86426279 | ATGACCAAAAAACAG[A/C]AAATGAGGAAGGCTT | 70348 |
rs30479430 | snp | G/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86444303 | TTGTTTGGGGGGAGG[G/T]GGGCAGGATGACAGG | 70348 |
rs30483399 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86315769 | TTCCTACATAAAGCA[A/G]ACTAAGAGTTAAGTA | 70348 |
rs30485298 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86434315 | TATCTTTAAACAGCA[A/T]TTTAATTACCACAGA | 70348 |
rs30485553 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube2cbp | Mm_Celera | 9:86309834 | GATTAAGGCAGAGCA[A/G]CATTTGAGACACTGG | 70348 |
rs30486292 | snp | A/C | 0.484429 | 0.0868505 | intron-variant | Ube2cbp | Mm_Celera | 9:86358816 | GCAGCATAAACCTGC[A/C]CTTAGACATTACTAA | 70348 |
rs30487632 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86403939 | CTCGGGAGGCAGAGG[A/C]AGGTGGATTTCTGAG | 70348 |
rs30500678 | snp | A/T | 0.33241 | 0.236027 | synonymous-codon, intron-variant | Ube2cbp | GRCm38.p3 | 9:86451959 | GGTTCTCACCAAAAG[A/T]GAGGTGGGCGTTATG | 70348 |
rs30511001 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86412434 | TTGAATTGGCCCACC[C/T]CAGCATCTACACCAT | 70348 |
rs30513861 | snp | C/T | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86310436 | TTTGTTTCTTTTTTT[C/T]TTTTCTTTTCTTTCT | 70348 |
rs30516705 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ube2cbp | Mm_Celera | 9:86312709 | TTTTCTCTGGAAGAG[A/C]TGTGAGGGGGTTCAT | 70348 |
rs30518776 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86371215 | AGGTCCCTCTACATG[C/T]CTGGGATTGAAGTTG | 70348 |
rs30519706 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86338348 | TAGAGCTCATAGTCA[A/G]AGCCTGGAACCAGAC | 70348 |
rs30521053 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86377606 | GGCTTCCACTTCTAA[C/T]GAAAATGGTGATATT | 70348 |
rs30522195 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Ube2cbp, Dopey1 | GRCm38.p3 | 9:86466865 | CCCTTTCGAATACGC[A/G]TTTGAAAGACGGCTA | 70348 |
rs30524192 | snp | C/T | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86411369 | TCAGGTCCTAGCACT[C/T]GAGCTTGGCATTTCA | 70348 |
rs30524989 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86444519 | CACAAAGTCCATCGC[A/G]CTCTTCTCCTAGAGT | 70348 |
rs30526305 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Ube2cbp | Mm_Celera | 9:86311793 | GCTAAGCAATGAGAT[A/G]CCCTAATAGGATGGA | 70348 |
rs30529168 | snp | A/G | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86421611 | ATATCCACCCATGAG[A/G]AAAAAAAAAATGGTT | 70348 |
rs33621606 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Ube2cbp | Mm_Celera | 9:86394634 | ATTCATATGTCTTGC[A/G]ATTTCAAATGATTTA | 70348 |
rs33621835 | snp | A/G | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86400387 | ATAAGCCACAATTAC[A/G]CTTATACCTAAACCA | 70348 |
rs33621845 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Ube2cbp | Mm_Celera | 9:86444030 | TTGAAGTCAGTTTCT[C/T]ATCAGTAGCAATACC | 70348 |
rs33630256 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86418729 | AACAACCAAGGGGCC[C/T]TGCAGTCACACTTCC | 70348 |
rs33637724 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86422487 | GCTTCCTCATGTTAC[C/T]GAGGCAGTTGCAAGG | 70348 |
rs33639251 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86368038 | AGAGCCTTTGGGAGA[C/T]AATAGTGCTTAACCC | 70348 |
rs33642151 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86426743 | GAGAAAGGGTGCTCA[C/T]TGGCTTGTTGCCCAC | 70348 |
rs33642571 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86452262 | AAAATCAAAGTACTG[C/T]TTAGCCGGTAATCAA | 70348 |
rs33643494 | snp | A/C | 0.304688 | 0.243945 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86358618 | ATCTGTGTATGCATG[A/C]AAATTACAAATCATA | 70348 |
rs33649339 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86387221 | CTCTGAGAAGCTCCA[C/T]TCAGAAGCTGACTGA | 70348 |
rs33655085 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86325592 | ATCTTGCCTGCTTCC[C/T]TGAGTGGGACGGGCT | 70348 |
rs33656645 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86338154 | GCAAAACTGCACAGC[A/C]CCAGAACTGCTTTGG | 70348 |
rs33660410 | snp | C/G | 0.5 | 0 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86403227 | TTAGAAGCGTGGTGG[C/G]GGTGGGGAGGATGTG | 70348 |
rs33660933 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86338388 | TGGACCTGCAGGACA[A/G]ACAAGCATTTTGGCC | 70348 |
rs33661763 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Ube2cbp | Mm_Celera | 9:86307474 | TCCCAGGATTTAGAG[C/T]GGTTAACATTCAGCT | 70348 |
rs33662324 | snp | A/C | 0.415225 | 0.187619 | intron-variant | Ube2cbp | Mm_Celera | 9:86315928 | AGGAGTCTCTTCAGC[A/C]AAATTCTTTGGCTAG | 70348 |
rs33662612 | snp | C/T | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86311853 | TGGAGGAAAACTCAT[C/T]CCCTGAGTTATGAAA | 70348 |
rs33664495 | snp | A/C/G/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86450166 | ACCTGCTTTACACAG[A/C/G/T]TCTTCATGCACCAGA | 70348 |
rs33665435 | snp | G/T | 0.396694 | 0.202437 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86390864 | ACCTAATCACAGCAT[G/T]CTTAGGTCTTACAGA | 70348 |
rs33665761 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86450532 | ATTTTTGTTTACTTT[G/T]TCCTTTTCAGGATTC | 70348 |
rs33668018 | snp | A/G | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86377958 | GATGTCAGAAACGCA[A/G]CTGAAAAACTATAAT | 70348 |
rs33675021 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86372560 | GGAGGAGAACTACAT[C/T]GTGTGCGCGTGTTTA | 70348 |
rs33680557 | snp | A/G | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86314136 | GCTACCTTCTACTTT[A/G]ACATCCATCAGTATA | 70348 |
rs33683003 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86322795 | GTCTTGGCTTCTTCG[C/T]CAGTAACTGAGCTTC | 70348 |
rs33685954 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86434511 | TGACCCAGCTCCACA[A/G]CATTCTGACCTCCAC | 70348 |
rs33686495 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86316055 | AGGTAAGATGTAAAA[A/T]TGTATAGGTATTCTC | 70348 |
rs33693207 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Ube2cbp, Dopey1 | GRCm38.p3 | 9:86466265 | TGTGAGTACAGGGCC[A/G]TCTAGAGCTATGTGG | 70348 |
rs33702692 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86377827 | ACCAAGATGAAAGAC[A/G]TGAACTTAGATCTTG | 70348 |
rs33704676 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86324806 | AAATAATAGATTTTT[A/T]AAAAAAAATTAACCC | 70348 |
rs33706119 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86438311 | AAATACAAGGAGGGA[C/T]GGACGAATGAGCGCA | 70348 |
rs33710468 | snp | A/G | 0.5 | 0 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86442158 | GAGTTGGCCTTTGAA[A/G]GATAATAAACCTGGG | 70348 |
rs33712791 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86409485 | ACAGGGACTCCAGGT[A/G]AATTTTCTATTGAGC | 70348 |
rs33715788 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86463863 | ATGTCAACACAGTTC[A/G]AGAAACAGGGATATT | 70348 |
rs33715827 | snp | A/C | 0.265928 | 0.249492 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86451327 | CACACACTCCACATT[A/C]CCAGACAGCTATGTG | 70348 |
rs33719160 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86391265 | CCTCACCATATCAAA[C/T]GCATATTCATTCTGT | 70348 |
rs33720834 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86367912 | TGGGATAAATGGCAT[C/T]CCCATGACAGTCAGT | 70348 |
rs33724863 | snp | C/G | 0.345679 | 0.230967 | intron-variant | Ube2cbp | Mm_Celera | 9:86452840 | GTTCCATGAACCACA[C/G]GGTCTCCATAAGATG | 70348 |
rs33726022 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86315997 | TAAAGTCACAAAAGC[A/C]CCACCAAAGCTGGCA | 70348 |
rs33728757 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Ube2cbp, Dopey1 | Mm_Celera | 9:86466484 | GGGTTGGCTTTGTGG[C/T]TAAGAGCACTTGGTT | 70348 |
rs33731915 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86345224 | GAGTTGCATGTTCCA[C/T]GGCAGTTCTATCTTT | 70348 |
rs33735267 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86393476 | ATAGCAAAACTAAGT[C/G]TTTAAGAGCCAGCTC | 70348 |
rs33735925 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86405050 | CTGGAACTCACTATG[C/T]AGACCAGGCTGGCCT | 70348 |
rs33736638 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86371239 | GAAGTTGGTTAACAA[C/T]AGAGAAAGAGTGATA | 70348 |
rs33740835 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Ube2cbp | Mm_Celera | 9:86324946 | TGTCAGATTCCACAG[C/T]TGGCTCCAGAATAAC | 70348 |
rs33740947 | snp | A/G | 0.444444 | 0.157135 | utr-variant-5-prime | Ube2cbp | Mm_Celera | 9:86464873 | CTAGAACCCGGACAG[A/G]GTGGGAGCACGTGCG | 70348 |
rs33741471 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86393521 | ATAGAGCTTTCATTT[C/T]GAATCACTATATACA | 70348 |
rs33742574 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86377684 | AGAGGGTGAGAGCAT[A/G]GAAGTCATTCAGTGC | 70348 |
rs33742972 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86426312 | TTAGCTTCCACTTTA[C/T]AGTCCCTCACTGACC | 70348 |
rs33745705 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86417216 | TATACATTTATAGCC[C/T]ATTTTCACATCTTCT | 70348 |
rs33746458 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86316196 | CCCGGTTCTTTTGTT[C/T]GTTGAAGCGTTCGAT | 70348 |
rs33746748 | snp | A/G | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86440575 | ATTTTTTTTTTCAGT[A/G]CAACTCTTACCTGCT | 70348 |
rs33748694 | snp | A/G | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86421365 | GTCAGTCCTGATAAA[A/G]TTATGGAAATGGGCA | 70348 |
rs33748818 | snp | A/G | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86420476 | GGAGGTATAGGCGAG[A/G]ACCTGAGTTCCAAGT | 70348 |
rs33754770 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Ube2cbp | Mm_Celera | 9:86312209 | CATAGTATACCCTAT[A/G]ATGAGTGTACCAGGG | 70348 |
rs33755327 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86335200 | CTGAACAGGGAATAG[A/T]AGGGAGGGATGAAGG | 70348 |
rs33759689 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86322707 | CCTCATGTAGAACTG[C/T]CAGGCCATCTGGCTC | 70348 |
rs33763285 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86400540 | CACTCAGGCTTCATT[C/T]CAGGGATGCAGGGAT | 70348 |
rs33763951 | snp | C/G/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86444517 | TCCACAAAGTCCATC[C/G/T]CGCTCTTCTCCTAGA | 70348 |
rs33764847 | snp | A/G | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86420845 | TCAAAGAAAGAAAGA[A/G]AGAAAGAGAGAGAGA | 70348 |
rs33769115 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Ube2cbp | Mm_Celera | 9:86435249 | CTATTAAGTAGGAGG[C/G]CAGTCATTTCAGCCT | 70348 |
rs33769295 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86345168 | CCAAAACACCTCAAC[A/G]AGCCCACTCAGAATG | 70348 |
rs33772881 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86409197 | TCACACACAGAATTA[C/T]TAACACCATCTGAAA | 70348 |
rs33773550 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86410433 | CAGCGGGTGAGGCAA[A/G]TGGGAAAAAAAAGAA | 70348 |
rs33773957 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86421981 | TACATATTCAACTTT[C/T]AGTTCATTTGAATCT | 70348 |
rs33776884 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ube2cbp | Mm_Celera | 9:86463729 | TCACCATTCATTCAT[A/C]GCCACTGTTGGACTG | 70348 |
rs33896648 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86392660 | TGTGGTTTTCACACT[A/G]TTGAGAGTTTAGTTG | 70348 |
rs33896654 | snp | A/G | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86415103 | AGAGAGAGAGAGAGA[A/G]AGAGAGAAAGAAAGA | 70348 |
rs36241164 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86322668 | AAAGAGAGGAACTGC[A/G]GAACACAGTATAACC | 70348 |
rs36243240 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Ube2cbp | Mm_Celera | 9:86308137 | ATGACGTAATCTAGT[G/T]CATGCTTCCATTTGT | 70348 |
rs36251065 | snp | A/T | 0.297521 | 0.245442 | intron-variant | Ube2cbp | Mm_Celera | 9:86369720 | AAGCCATGGGGAAAA[A/T]TCTAAGTAAGGAATG | 70348 |
rs36252016 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Ube2cbp | Mm_Celera | 9:86377358 | AAAGATACTTCAAAG[A/G]GAACAAGGAACCAAA | 70348 |
rs36255681 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Ube2cbp | Mm_Celera | 9:86412922 | CAGAGACAGGTTGCA[A/G]AGAGAACAAGCTAGA | 70348 |
rs36256246 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ube2cbp | Mm_Celera | 9:86331161 | CCATCTTTCACTGAA[C/T]GTGGCTCCCTCTGCG | 70348 |
rs36256622 | snp | C/T | 0.18 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86421532 | CAAAGTACACATAAC[C/T]AGAAAACAACCCGCA | 70348 |
rs36258075 | snp | C/G | 0.197531 | 0.244432 | intron-variant | Ube2cbp | Mm_Celera | 9:86375943 | TATGATGTTGCTATC[C/G]ATTCTGGTGCAGAGA | 70348 |
rs36262726 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86334921 | ACTCATAGCCTCGAC[A/G]ACAAGTCACTGGTGT | 70348 |
rs36263024 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Ube2cbp | Mm_Celera | 9:86310650 | TGTGACTCTGTTCTG[A/T]GCACACAAATATGAA | 70348 |
rs36267457 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ube2cbp | Mm_Celera | 9:86317974 | GGTTCTGTAGTTCCC[A/G]CCAATCCAGTGCCTC | 70348 |
rs36271657 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86331635 | CTGCTTCTCATCGAC[A/G]CACATATTGATGCAG | 70348 |
rs36274278 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86321598 | AGGCTGAGATCAGCT[C/T]CCTGCCATGCCTAAC | 70348 |
rs36274386 | snp | C/T | 0.18 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86371646 | CAAGCCACTACTTAA[C/T]TCTCATCCTTAGTTT | 70348 |
rs36274467 | snp | C/T | 0.489796 | 0.070696 | downstream-variant-500B | Ube2cbp | Mm_Celera | 9:86306988 | CAGCAGAGATGACTG[C/T]AGATGCCTGTCCTTC | 70348 |
rs36280840 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86330515 | CATTAACACATGAGA[G/T]CATTTACTAAGAGTC | 70348 |
rs36283723 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86322125 | TAGGTCTGAGTCCTG[A/G]AGCCACTGACTAGAT | 70348 |
rs36284401 | snp | C/T | 0.197531 | 0.244432 | synonymous-codon | Ube2cbp | Mm_Celera | 9:86372479 | CCAGGAGCTAGCAAG[C/T]CTGAAACACACAGAT | 70348 |
rs36291332 | snp | C/T | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86374821 | CTGGTCATGAGCCTT[C/T]GGGAAGGGCATCTTG | 70348 |
rs36297263 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Ube2cbp | Mm_Celera | 9:86366996 | ACTAATCATCTAGGG[C/T]TAAGAGATAAAGCCT | 70348 |
rs36299857 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Ube2cbp | Mm_Celera | 9:86371374 | ATTACACTGGAACAC[A/G]TGCTTTTGATCCATT | 70348 |
rs36305247 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86388835 | GAGCCCCCATTTGCA[C/T]TTCATTGTAATCTTC | 70348 |
rs36307713 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ube2cbp | Mm_Celera | 9:86330348 | TCTCTCGGCATCCTC[C/T]GATGAGGTAGAGGGC | 70348 |
rs36312400 | snp | C/G | 0.165289 | 0.235211 | intron-variant | Ube2cbp | Mm_Celera | 9:86370774 | TAAAAATCTCAAATA[C/G]TCCATGAGAGACAGA | 70348 |
rs36313044 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86361885 | ACCTGCATCTTAGAA[A/C]ACATTTGAGAATGAA | 70348 |
rs36314862 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86307945 | AGATCTGAGCGGGAT[C/G]GGGCCAAATCTGGTC | 70348 |
rs36315243 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86325174 | AATCCCTTGCAGTTA[C/T]GCTCATCACAGCTCA | 70348 |
rs36315379 | snp | C/G | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86362898 | GGGTATGAACTTGGT[C/G]AGCCAAATCTACTTC | 70348 |
rs36317785 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ube2cbp | Mm_Celera | 9:86339137 | GAAGAAGCTTGTGGG[A/G]TAAATTCTCTCTCTA | 70348 |
rs36328901 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86356167 | GGTACCTGATGTGTG[C/T]AAAGTGGAAAGTTAG | 70348 |
rs36329398 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86362885 | AATCAAAAGCCATGG[A/G]TATGAACTTGGTGAG | 70348 |
rs36330488 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86369395 | AAGAGGACAAATGGA[C/T]GCAACCATTACACAG | 70348 |
rs36332193 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ube2cbp | Mm_Celera | 9:86329865 | CATTGGCAGCATGAA[C/T]ACTGTTTTGAGTGTG | 70348 |
rs36332449 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86321878 | TTTTTAAAGGAAGAT[G/T]TACAAAGGGCTGGCT | 70348 |
rs36337945 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86318180 | CCTACGCTACAGCTC[C/T]ATCTTATGTCTCAGG | 70348 |
rs36338617 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Ube2cbp | Mm_Celera | 9:86421591 | CAACAAAAGCAAGAA[A/T]GCAAATATCCACCCA | 70348 |
rs36338941 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86361981 | ACTGTGCTAAGTGCA[A/G]GTTAATAAGAAACAA | 70348 |
rs36340161 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86312052 | GAGGAGGAGTCCCTG[C/T]CATGGCAACAGGTGC | 70348 |
rs36340625 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86331375 | ATGGTTCTGCAATAG[A/C]AGGTAAAATCACTAC | 70348 |
rs36343316 | snp | C/T | 0.375 | 0.216506 | missense | Ube2cbp | Mm_Celera | 9:86425351 | GGCACTGGGCAATAA[C/T]GCTCTGAAGGAACTG | 70348 |
rs36345622 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86362255 | AAGCTTCCTGGGTAC[G/T]CTGACATACAAGAAG | 70348 |
rs36345674 | snp | A/T | 0.345679 | 0.230967 | intron-variant | Ube2cbp | Mm_Celera | 9:86425608 | ATCCCATACATAACT[A/T]TTCCCCTGTGATAGT | 70348 |
rs36345729 | snp | A/T | 0.42 | 0.183303 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86374556 | CCCACATTCAGTATT[A/T]TTTGCCTTTGAAGGT | 70348 |
rs36349346 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86318199 | TTATGTCTCAGGTAG[C/T]GATAATGTACGTGCT | 70348 |
rs36350811 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86330339 | TTTTTGTATTCTCTC[A/G]GCATCCTCTGATGAG | 70348 |
rs36357600 | snp | C/T | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86374615 | TGTTTAGAAACCAAT[C/T]TAAGCACCCAGAAGT | 70348 |
rs36360079 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2cbp | Mm_Celera | 9:86363141 | TACACCTACTACCCT[C/T]AGACATTGTGCCAGG | 70348 |
rs36361934 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Ube2cbp | Mm_Celera | 9:86371745 | CATGAGCAGCAGGGA[A/G]CTATACAAATAAATA | 70348 |
rs36362412 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Ube2cbp | Mm_Celera | 9:86359669 | TTAAGAGAAAAAAAG[C/T]AACCCACAACTTTCT | 70348 |
rs36362523 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86378171 | ACTAAATGGACTGCT[G/T]CAGGGTTTCTGGTAA | 70348 |
rs36369101 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86316732 | GGTAGGAGATGAAGC[A/G]TTTCCTTGTGTAAGA | 70348 |
rs36369545 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86321513 | CCATGAAGCCAAGAG[A/G]TGTAAAAACTTCCTG | 70348 |
rs36370367 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86339774 | GAGCTACTGAGCTCA[C/T]ATCAGGCTGGCTGAG | 70348 |
rs36370975 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ube2cbp | Mm_Celera | 9:86359079 | ATACAAAGACCAAGA[A/G]TCTATCATTCACAGA | 70348 |
rs36372110 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Ube2cbp | Mm_Celera | 9:86352699 | TCTTTCTTATGATTC[C/T]ACCTTCTTACTACCA | 70348 |
rs36372861 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Ube2cbp | Mm_Celera | 9:86308795 | TACTCTTCATGTGGT[A/G]CAGCAAGGAATGCAC | 70348 |
rs36373482 | snp | A/T | 0.426035 | 0.177515 | intron-variant | Ube2cbp | Mm_Celera | 9:86363377 | TCAGTAATGGCCACT[A/T]TTAAGAAAATTGTAT | 70348 |
rs36374513 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86361865 | GGTGGGTTAGGGCAA[C/T]GAGCACCTGCATCTT | 70348 |
rs36375639 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86310522 | GAACACATGCCTACA[G/T]CTGAACCTCTAGGCT | 70348 |
rs36376274 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86312321 | CAGTCACTTGTCTGA[A/G]TTCCAGCCTTCACCA | 70348 |
rs36378217 | snp | A/C | 0.486111 | 0.0821678 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86395093 | TATTCAAACATCTGA[A/C]GGCTAGGGATAACAT | 70348 |
rs36382636 | snp | G/T | 0.486111 | 0.0821678 | intron-variant | Ube2cbp | Mm_Celera | 9:86321484 | GAAGGGACTAGAGAG[G/T]CAGAGATAAAAGTCC | 70348 |
rs36385317 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86419993 | TGAGTGACTTGGTTG[A/G]TAAAGTCCCTCTGCA | 70348 |
rs36386377 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Ube2cbp | Mm_Celera | 9:86377381 | GAACCAAACATCAGT[C/T]GAAAGCCATTTCCTT | 70348 |
rs36386884 | snp | A/C | 0.46875 | 0.121031 | intron-variant | Ube2cbp | Mm_Celera | 9:86376591 | GACCCTGGAGCCGGG[A/C]TGTGACGGGAAAGAA | 70348 |
rs36393225 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86319873 | CTCCCTAGTTAAGAA[G/T]AAAGTTGATTCCTTC | 70348 |
rs36396009 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Ube2cbp | Mm_Celera | 9:86366218 | CTGTGCTGAATATGT[A/G]ACTTTTCTACTATAA | 70348 |
rs36398134 | snp | A/T | 0.18 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86414197 | AATGAAGTACAAAAG[A/T]GTCATCATGAAGCCC | 70348 |
rs36398645 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86377200 | CCCACCCATGACTCA[A/C]ACATCAGTGCACATC | 70348 |
rs36398961 | snp | A/C | 0.497041 | 0.0383476 | intron-variant | Ube2cbp | Mm_Celera | 9:86330136 | CCAAGACACATGGGA[A/C]TGGCTCACTGGAGCC | 70348 |
rs36402060 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2cbp | Mm_Celera | 9:86364845 | CTGACAAGCACCCAC[A/G]TCTTTATTATCTCTG | 70348 |
rs36403421 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Ube2cbp | Mm_Celera | 9:86316752 | CTTGTGTAAGACACT[C/T]GTAGTAAACATGTGT | 70348 |
rs36408919 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Ube2cbp | Mm_Celera | 9:86421740 | CATATCCTCCAAACC[A/G]TGTCCACGCAAGATG | 70348 |
rs36413504 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86318209 | GGTAGTGATAATGTA[C/T]GTGCTGTGAGAAGTC | 70348 |
rs36418619 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Ube2cbp | Mm_Celera | 9:86370193 | GAATATGTCTCTCCA[A/G]TGCTGCCAGGAGCCT | 70348 |
rs36422264 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Ube2cbp | Mm_Celera | 9:86389000 | AGCATGAAAAAGAAA[C/T]GTAAAGTCATGATTA | 70348 |
rs36432102 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Ube2cbp | Mm_Celera | 9:86416536 | TTGTCCTTGGTGGTG[A/G]ACGATCAAACAGTAA | 70348 |
rs36436762 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86369889 | TTGCACCAAAAACGA[C/G]ACGTTATAATACAGA | 70348 |
rs36436889 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86316745 | GCATTTCCTTGTGTA[A/G]GACACTCGTAGTAAA | 70348 |
rs36446200 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Ube2cbp | Mm_Celera | 9:86331811 | AGGTGTATCACAAAC[C/T]CCAAAAATAAAGTCA | 70348 |
rs36451422 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Ube2cbp | Mm_Celera | 9:86415208 | TACTTCTATACTTCT[G/T]GGCCATGCATTGGTA | 70348 |
rs36451552 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86426021 | AACTCACTGACAACT[C/T]AACATTCATTCACAC | 70348 |
rs36454661 | snp | G/T | 0.396694 | 0.202437 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86423395 | GAAGGTACATTGATG[G/T]GTTTCTAGGACACTC | 70348 |
rs36454950 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86340904 | GATGTTAAGTGCTAA[A/G]CAACACAGAAAAATA | 70348 |
rs36465312 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Ube2cbp | Mm_Celera | 9:86413440 | CAATAAAACGCTTTT[A/T]AGAAAAAGAAATTTC | 70348 |
rs36469128 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Ube2cbp | Mm_Celera | 9:86308232 | TTCTGGCCTTAACAC[C/G]GTTGGTAAGTACCCC | 70348 |
rs36469259 | snp | A/T | 0.18 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86370803 | GAAGAGAATATACTA[A/T]GAATGTTGCTCTCCT | 70348 |
rs36482861 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86316398 | AGTCCCAGTGGCTAG[C/T]TCCTCGAACTGCTGT | 70348 |
rs36484486 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86339720 | AGAGAAAGCATTACA[C/G]AAAAAGAGACAAAGA | 70348 |
rs36491187 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86322514 | ACAACCAACGCTTAA[C/T]CACACTTTGTTGGAG | 70348 |
rs36491443 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86322708 | CTCATGTAGAACTGT[C/T]AGGCCATCTGGCTCA | 70348 |
rs36494018 | snp | G/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86356106 | CAGATGTAACTCGGT[G/T]AAAGCTAATGGACCA | 70348 |
rs36494042 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86321429 | AGTGGGAGTGTCAGG[A/T]GAGCCTACAGTGGTG | 70348 |
rs36495711 | snp | A/T | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86327234 | TGGGGACAAGAAGAA[A/T]GTGAGGACCCTGCAT | 70348 |
rs36497428 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Ube2cbp | Mm_Celera | 9:86415982 | ATCGCTTTCCATCAA[A/C]AATCAGTGGTATTTT | 70348 |
rs36499145 | snp | A/T | 0.46281 | 0.131194 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86412887 | TCAGCAGAGAAGGAA[A/T]TTTTACCTGGACAAT | 70348 |
rs36502613 | snp | C/T | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86308625 | AGTAAATTCATTCCA[C/T]TCTTAGAGAAGTATC | 70348 |
rs36503707 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86360665 | TCATCACCAGGAGGG[C/T]TCACGAGAGTTTCTC | 70348 |
rs36505180 | snp | C/T | 0.5 | 0 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86316547 | AGTGCTTTCCACCTT[C/T]CAAAATAGCATCAAT | 70348 |
rs36506268 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86337048 | GGCTGTGTCAGCCAT[C/T]CCTAAGACCTTGCCT | 70348 |
rs36508608 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86340341 | TTTGGATTATAACTG[C/T]TTTGAATCGATCATA | 70348 |
rs36513973 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86338847 | CAAGGTTAATACAAC[A/G]GCTTAGCGTCTGTTC | 70348 |
rs36515583 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Ube2cbp | Mm_Celera | 9:86425062 | TCTGACTGCACCCCT[A/G]AAGAACCTAGGATGC | 70348 |
rs36528060 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86331832 | AATAAAGTCACAAAC[C/T]ATTCCTACCTGCAGA | 70348 |
rs36529601 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86333128 | ATGATAATGAATACC[C/T]GTAGTGGTAAAAAAA | 70348 |
rs36533735 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86321854 | TCATGTTTCTATTTT[C/T]GTAGTTATTTTTTAA | 70348 |
rs36537343 | snp | C/G | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86356187 | TGGAAAGTTAGGTTT[C/G]ATGTGGCAGCACTAG | 70348 |
rs36538451 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86358444 | GAGGCTAATTAACAA[A/G]CCAAAATAATTAGAA | 70348 |
rs36539811 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86344326 | TCTAAATACATGCAT[A/G]CACTAACAAGACAGA | 70348 |
rs36540415 | snp | C/G | 0.32 | 0.24 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86380819 | CTCTCTCTCACTGTC[C/G]ACTACATTTTTATAG | 70348 |
rs36540938 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86335114 | GGGGAAACTTCCCCA[A/G]TTATTCTTCTCAATA | 70348 |
rs36541013 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86415300 | GGGAAAGCAGTGGAG[A/G]CACAAGTGAGTCTGT | 70348 |
rs36542140 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86414779 | ATTTAATATCCATAA[C/T]GCAATGTGGAGAAAT | 70348 |
rs36542383 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ube2cbp | Mm_Celera | 9:86308529 | GTCCTGAGGTGACAG[C/T]AAAGCCAGAAAGAGA | 70348 |
rs36556005 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Ube2cbp | Mm_Celera | 9:86420216 | CAAGGCTATCCTCTT[C/T]TACGCATGTGCCAAT | 70348 |
rs36569474 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86321112 | GATCATGTATGGATC[A/G]TAACACTGTACCTAG | 70348 |
rs36576215 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Ube2cbp | Mm_Celera | 9:86391349 | TTTAACCCTTGAGGT[A/G]ATGTGCTGGCTAGTT | 70348 |
rs36579015 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86334964 | GTTTCTACCCATGCA[C/T]TTTGAAAATGAGTGC | 70348 |
rs36583900 | snp | C/T | 0.152778 | 0.230321 | missense | Ube2cbp | Mm_Celera | 9:86422952 | AACTTCCTGCTACAA[C/T]TGGAACTTCTCAGAG | 70348 |
rs36588150 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ube2cbp | Mm_Celera | 9:86310684 | TTGGAGAGGAAAGAA[C/T]CTGAGCCAAGAGATC | 70348 |
rs36588231 | snp | A/C | 0.18 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86424772 | GAGAGTGTAGATGCA[A/C]CAAAGCCAGCATCTT | 70348 |
rs36601971 | snp | C/T | 0.18 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86422584 | TCACAGTTGTTGCAG[C/T]CTGACTTAGCACCAC | 70348 |
rs36602935 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86374729 | TTCAAACTTGCATCT[C/T]CTTAAAAGCCACAGG | 70348 |
rs36603253 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Ube2cbp | Mm_Celera | 9:86358149 | GACTTAGATGGAAAC[G/T]CTACATTCAGAGAAC | 70348 |
rs36605299 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86323892 | ATAGTAGAGAGAACA[A/G]TGTAACTAGCATGCA | 70348 |
rs36610808 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Ube2cbp | Mm_Celera | 9:86365207 | TAATAATATTTCTCT[C/G]TGTGTGAGAATACAT | 70348 |
rs36616014 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86326544 | CAGTGCAGACCCCTG[C/T]GGCACGTTAAATAAG | 70348 |
rs36616191 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ube2cbp | Mm_Celera | 9:86312255 | GCTACCAGGAACATG[A/G]CAACCAGAGGCTCCA | 70348 |
rs36619614 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86389080 | CACCTGGACAGTATT[C/T]AAAGTTCCTGCAAGA | 70348 |
rs36624512 | snp | C/T | 0.5 | 0 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86373505 | GATACACGAACAGTA[C/T]AGCTTTTGCTTCTGT | 70348 |
rs36628137 | snp | C/G/T | 0.486111 | 0.0821678 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86331774 | AATCCTCATTCAATA[C/G/T]GAGTAAGTAGCTCTC | 70348 |
rs36628541 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86356153 | GGTAGATTTGACATG[A/G]TACCTGATGTGTGCA | 70348 |
rs36641718 | snp | A/T | 0.473373 | 0.11227 | intron-variant | Ube2cbp | Mm_Celera | 9:86314431 | AACAGGAGGAATCAA[A/T]AAAAAAAATTATTCT | 70348 |
rs36644031 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86314392 | AATAATCAGAATCCA[G/T]TCTATAAATGCATGG | 70348 |
rs36651406 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | Ube2cbp | Mm_Celera | 9:86308273 | CAGGCCATGCTGATA[A/C]TTTTAATCACATGCA | 70348 |
rs36651942 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86323145 | ACGCACTGCTCTGAT[A/G]GGGAGTGCATGAAGT | 70348 |
rs36654117 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86365652 | AAAATTTACCCACGA[C/T]CGATCAAGGCAAGTA | 70348 |
rs36654471 | snp | A/C | 0.18 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86370664 | TTCAGGTTGCTTTGT[A/C]ATAAAATTATTCTCA | 70348 |
rs36659673 | snp | C/T | 0.18 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86422376 | GGAATAGCACCTACT[C/T]CGCAAAGCTGCTTTA | 70348 |
rs36663062 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86412585 | TCTATGTTAACCTCG[A/C]AACATGGCTGCTCTG | 70348 |
rs36681100 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86361507 | AGAGTCACAGTATGC[C/T]GCCTGGGTGAATAAC | 70348 |
rs36681724 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86362290 | GCTATCTGCAATCAC[A/G]CCATGGCCCATTCTC | 70348 |
rs36685733 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86410876 | TTGAAGCCTGCCTGA[A/G]CTACAAGGCAAGATC | 70348 |
rs36686663 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Ube2cbp | Mm_Celera | 9:86325406 | AGTGGCCTCCCCAAA[A/G]GCTGTTCCTGTCTCT | 70348 |
rs36687222 | snp | C/G | 0.42 | 0.183303 | intron-variant | Ube2cbp | Mm_Celera | 9:86359246 | CTTTCAAGAGAAACA[C/G]ACATCAACGGACGGC | 70348 |
rs36689167 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86328748 | CCCAAACAAACATGA[A/G]TACATGAGAGTCATG | 70348 |
rs36690373 | snp | A/C | 0.197531 | 0.244432 | intron-variant | Ube2cbp | Mm_Celera | 9:86412041 | CTTAGAAGAGCAGGT[A/C]CTGTACCTCACCTGG | 70348 |
rs36695476 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Ube2cbp | Mm_Celera | 9:86366131 | TTAGATGTTACTTTG[G/T]ATAAATATTAATAGC | 70348 |
rs36701318 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Ube2cbp | Mm_Celera | 9:86307895 | GAAAAAAAAAATCCA[C/T]AGTGCTTTAATGATG | 70348 |
rs36709324 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86338865 | TTAGCGTCTGTTCCT[A/C]ACATTACATGCAGCT | 70348 |
rs36713608 | snp | A/G | 0.18 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86345345 | GCCTGACGTAGTTCT[A/G]TATCACACCAAAATG | 70348 |
rs36713643 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86311827 | GTTTAAGATGTATGC[C/T]TAACACCTGCTGGAG | 70348 |
rs36715888 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86326016 | CTGGAAAGGCGAAAG[C/T]ACTGGAAAGCTACCC | 70348 |
rs36716116 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ube2cbp | Mm_Celera | 9:86326394 | TATTCATTATCACAA[A/G]AGTAAGAGAGACCAG | 70348 |
rs36716850 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Ube2cbp | Mm_Celera | 9:86359068 | GACATGTAGACATAC[A/G]AAGACCAAGAATCTA | 70348 |
rs36717311 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86312028 | AGGGATTCTGGCAAA[C/T]GGTCTAAGGAGGAGG | 70348 |
rs36718075 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86339574 | AAAATAGGAACGTTT[C/T]AATACTCTAACAGAG | 70348 |
rs36719548 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2cbp | Mm_Celera | 9:86328480 | TTCAGACATTCCAGC[C/T]TCATGTTCCCACTCA | 70348 |
rs36725545 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86329087 | AAATAGCTCTGAACC[C/T]TTTTCCAAGTTCTGG | 70348 |
rs36726383 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86415440 | GGGGCTATGTAGAGA[A/G]CTACAGAACATGTCC | 70348 |
rs36728340 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Ube2cbp | Mm_Celera | 9:86363002 | CATGGCACTCCAACT[C/T]TTTCTGTAGCCTTAG | 70348 |
rs36729309 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86319282 | TATTTTCTATCCTTG[C/T]GTTGCATTTGATGCA | 70348 |
rs36731828 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Ube2cbp | Mm_Celera | 9:86413083 | GCAGAGGAATTTTGA[A/G]CCAGAAGAGCTGAGT | 70348 |
rs36733881 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Ube2cbp | Mm_Celera | 9:86417422 | TGTCTCCTGGAATGT[A/G]GCAGCAATGTTCTTG | 70348 |
rs36734503 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Ube2cbp | Mm_Celera | 9:86388497 | TTAACAAAAGAGTTT[A/G]CTCAAAAATCTTCTA | 70348 |
rs36739843 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86378240 | ACTTGTCTGTGCATG[A/G]CCACAGGACAGATCC | 70348 |
rs36748703 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86316335 | TTGCTCTGGAGTTTC[C/T]TGACCGAAGAGTTTG | 70348 |
rs36751809 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86335734 | CTGGAGAAAAACTCT[C/T]AGTCCTTGCAGTTTG | 70348 |
rs36752163 | snp | C/T | 0.18 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86425416 | TGACAATCCCATGAT[C/T]CTAACCAACAAGATA | 70348 |
rs36771083 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86388736 | TTACTCATTACCTGA[C/T]GCTTAGAGACCTCTG | 70348 |
rs36773665 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86309059 | GCCCTATTGTGTGTG[G/T]AAGCTAGCCTTGGGC | 70348 |
rs36783998 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86323966 | TACTTGCTTAGCATG[C/T]GCAAAGCCCCTGACT | 70348 |
rs36784255 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86356550 | TCATAGGATTTCCTG[A/G]GGAAGGCAGTAATGG | 70348 |
rs36790248 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86309853 | TTGAGACACTGGCTT[A/G]CCAACAAGAAAACTA | 70348 |
rs36790635 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86362971 | CCATCAGATCTACAT[C/T]AAAGCTATGGAAGGC | 70348 |
rs36794788 | snp | G/T | 0.18 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86370333 | TGGACTTCAACAGGC[G/T]TTGTTCATAAGACTC | 70348 |
rs36815068 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Ube2cbp | Mm_Celera | 9:86374225 | TTCTCCTAAAAGATG[A/C]AGACAGTACCATCTC | 70348 |
rs36821224 | snp | A/T | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86357997 | GGCAGATATGAAGAC[A/T]TGGGCCTGTCTATGG | 70348 |
rs36823170 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Ube2cbp | Mm_Celera | 9:86417179 | AACCTTCTAAGACTA[A/G]AGGAACTTTTTTCAA | 70348 |
rs36827409 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86420772 | GATTTTAATCAAACC[C/T]TCAAACATTTGGGAA | 70348 |
rs36828702 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Ube2cbp | Mm_Celera | 9:86418925 | CAAGAAAACTTCGGG[C/T]TATCACACACGAAAG | 70348 |
rs36831732 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86339006 | GGTAACATAGTCTGG[C/T]AGCTTTGATGGGAAT | 70348 |
rs36836857 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86329986 | CCAGCTAACAACTCA[A/G]AAGATTCAATCCCAC | 70348 |
rs36840741 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Ube2cbp | Mm_Celera | 9:86358051 | GGATATGTAAAAGTG[A/T]CAAACCTCAAACTAT | 70348 |
rs36844875 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86380580 | GCAGAAATCAGCCAG[A/G]GAGCAGCTAGAGCTT | 70348 |
rs36845453 | snp | C/G | 0.42 | 0.183303 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86411344 | TACCATTCTTGCCCA[C/G]GAACCAAATTCAGGT | 70348 |
rs36849145 | snp | A/G | 0.18 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86367306 | AATCTTAAGGTCTAG[A/G]ATCAGCCCTGGCTCT | 70348 |
rs36851680 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ube2cbp | Mm_Celera | 9:86340881 | ATGAAAAATAATAAC[A/G]ACATTAAGATGTTAA | 70348 |
rs36857110 | snp | A/C | 0.297521 | 0.245442 | intron-variant | Ube2cbp | Mm_Celera | 9:86369024 | ATTAGTTCCTCAGCA[A/C]TAGGACAGAATACCC | 70348 |
rs36861545 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ube2cbp | Mm_Celera | 9:86316427 | GTATCTTGGAAGCCA[A/G]GTCTTGAGCAGCTGT | 70348 |
rs36869558 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86319908 | GATTAATTAGAGAGA[A/G]GAAAGCAGAGCCTAA | 70348 |
rs36872667 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Ube2cbp | Mm_Celera | 9:86415176 | TTAACAAAGAAACAG[C/T]AACAGAAAAAGAACT | 70348 |
rs36888843 | snp | G/T | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86323595 | TTTCTTTGGGAAATA[G/T]TCTTAGTAGCATTCC | 70348 |
rs36890827 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Ube2cbp | Mm_Celera | 9:86338317 | AGTAGAAAAAAAAAA[A/G]GTCCTGGTCCTATGC | 70348 |
rs36892322 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Ube2cbp | Mm_Celera | 9:86360482 | GAGATCAGAGCCCAG[A/G]CCAGCTCCCACCTCC | 70348 |
rs36894222 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Ube2cbp | Mm_Celera | 9:86374457 | TTTTACAGACACCCT[C/T]AGTTTTGCTTTTCAG | 70348 |
rs36901268 | snp | C/T | 0.42 | 0.183303 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86316610 | CGCTCTGCCGTCCAT[C/T]GCCCATCTCTCCTTC | 70348 |
rs36908540 | snp | A/C/T | 0.473373 | 0.11227 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86328647 | GCCCAGACATAGACA[A/C/T]GAGAACCCAGAAGAT | 70348 |
rs36910893 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ube2cbp | Mm_Celera | 9:86329037 | CAATGCACTGCTTTG[A/G]TCTACACCATTGTCC | 70348 |
rs36914563 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Ube2cbp | Mm_Celera | 9:86319855 | TAGCTGGAATGAGGC[A/T]GCCTCCCTAGTTAAG | 70348 |
rs36920444 | snp | A/T | 0.197531 | 0.244432 | intron-variant | Ube2cbp | Mm_Celera | 9:86352740 | TCTAAACTTTAATGC[A/T]AAAACAAGACTTACT | 70348 |
rs36920529 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86337942 | TAGAAGAGACACCAA[A/G]AAGCCTAATGCTAAT | 70348 |
rs36928044 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86323541 | TAATTTAGACATAAA[A/G]CATTCCTCTGAAACA | 70348 |
rs36930012 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86310378 | CTGTGACAGGAAAAT[C/T]TGTTTCCAATTTGTT | 70348 |
rs36931407 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86312544 | GAAGAGTCTCTAAGC[A/G]TTTCATAAAAATCTA | 70348 |
rs36933582 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Ube2cbp | Mm_Celera | 9:86387077 | ATACTGCAACTAGCT[C/G]TCAAACATATCTTAA | 70348 |
rs36935451 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86376512 | CTATGTGATTACGAA[A/C]ATCTACATGGTTTCA | 70348 |
rs36937853 | snp | C/G | 0.21875 | 0.248039 | intron-variant | Ube2cbp | Mm_Celera | 9:86373797 | CAGATGATGTATTCT[C/G]CTGATCAGTTTCTGA | 70348 |
rs36938287 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86362190 | ACGAGGGCTCCTGGT[A/T]CTGAATCCATCTCCC | 70348 |
rs36942848 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Ube2cbp | Mm_Celera | 9:86405193 | ATTGCTCCTGCCTGC[G/T]GAGGACATTAGCATG | 70348 |
rs36944186 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86341159 | CAAAGAATTAAAACA[C/G]ACCAGTGATTCACTT | 70348 |
rs36967683 | snp | A/C | 0.46875 | 0.121031 | intron-variant | Ube2cbp | Mm_Celera | 9:86375468 | TGTCTGCCTCAAGAT[A/C]TTATTTTATTAAATA | 70348 |
rs36967743 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86336426 | CACATTTTTGCTGTC[A/T]TGTAAAATAGCAATG | 70348 |
rs36974119 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86358934 | TTATGGCAGCTGTCA[C/T]ATCAACAAAATTAGA | 70348 |
rs36977792 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86337151 | TTAATTGCCTGGCTG[G/T]CTCAGTCTAACATGA | 70348 |
rs36978443 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86323750 | ACCAATCTTTTCAGC[C/T]ATGTTCCTGTAAGCC | 70348 |
rs36981513 | snp | C/T | 0.18 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86378888 | GTCAAGGAAAACCTC[C/T]CAAGGACCAAAAAGT | 70348 |
rs36987147 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86420293 | TGAGTACAGTAACAG[A/G]AAAAGCTCTCTACAT | 70348 |
rs36995225 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86425485 | GCCTTTCTGACCACC[A/G]TCTGTTCCTTTAAAG | 70348 |
rs36998172 | snp | C/T | 0.18 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86316612 | CTCTGCCGTCCATCG[C/T]CCATCTCTCCTTCAA | 70348 |
rs37006471 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Ube2cbp | Mm_Celera | 9:86320206 | GCGAACATACCTCTG[C/T]TATGTATAAGCATCA | 70348 |
rs37018061 | snp | G/T | 0.197531 | 0.244432 | intron-variant | Ube2cbp | Mm_Celera | 9:86419617 | AGAAAAAGGCAATGG[G/T]ACTAAAATAGTTAAT | 70348 |
rs37020417 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Ube2cbp | Mm_Celera | 9:86317269 | TAAACAAAACAGCAA[A/G]ACAACAGGTCAGTAT | 70348 |
rs37021177 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Ube2cbp | Mm_Celera | 9:86328879 | GGATTTCTGTTTTCA[C/T]GCAGGGGTGTCAAAC | 70348 |
rs37024422 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86309968 | CTTTCTCACAGTAAC[C/T]TTGCAGATAAATGAG | 70348 |
rs37027362 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2cbp | Mm_Celera | 9:86379564 | ATAACCCTTTGGCAT[A/G]TTAATAAGTTTTATT | 70348 |
rs37033704 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86316973 | AACTATACTCAGTAC[C/T]GTTTGACGTTTGACT | 70348 |
rs37039718 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2cbp | Mm_Celera | 9:86362020 | TAATGAAGCTGTGTG[A/G]TTCAGTGACAGGGTG | 70348 |
rs37044527 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86318327 | ATAGACTTCTCATTT[A/T]AAAAAGAATCAGATT | 70348 |
rs37055262 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86361761 | GCTGTGAGGAGAGCA[A/G]GAGACACAGGCTGCC | 70348 |
rs37056835 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86360586 | TGTTCTTGTTTCTTA[C/T]AAACCCTACAGCTTC | 70348 |
rs37060301 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Ube2cbp | Mm_Celera | 9:86386729 | TGGGTGGGAGGAGCA[A/G]CCTGCCCTAGACAGG | 70348 |
rs37061173 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86377504 | CACTCTGTCCACTTT[A/G]CTAAACCTTTGCATC | 70348 |
rs37081477 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86337906 | CATGCCAAATAATGA[C/T]GACCAAAGACACCAA | 70348 |
rs37082358 | snp | C/T | 0.18 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86413928 | GTAACTACAGACTCT[C/T]ATCAAACAACATATG | 70348 |
rs37085297 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86380228 | CCTCTCTCATCTTTA[C/T]AAACTCATCTTTACA | 70348 |
rs37086936 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ube2cbp | Mm_Celera | 9:86327964 | CCTAAGCCATTCAAC[A/G]GAGCTATTATTCAGA | 70348 |
rs37088308 | snp | C/T | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86308808 | GTGCAGCAAGGAATG[C/T]ACCTGCTGAGTTTCC | 70348 |
rs37091137 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86320630 | CTGCAAGCAAATCTT[A/T]TAAAGAAGAGAAAGC | 70348 |
rs37099461 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86373715 | CCGTTTGAGGAGCAT[C/T]GGTGGTTGAGTGCAT | 70348 |
rs37102829 | snp | A/C | 0.473373 | 0.11227 | intron-variant | Ube2cbp | Mm_Celera | 9:86326259 | ACCAGGGATCCTACA[A/C]CCAATCACTAAACAG | 70348 |
rs37104565 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Ube2cbp | Mm_Celera | 9:86363389 | ACTATTAAGAAAATT[A/G]TATAAGTGAGAAGGA | 70348 |
rs37108251 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86331282 | TTCCACCTTAGCACC[A/G]AAGGGCAATTGAACA | 70348 |
rs37109804 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86327274 | CTCATATTCTCCATT[C/T]ATCTTTCCTTCCACT | 70348 |
rs37111516 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86326521 | AACGTAGCAGGGGTT[C/T]GGTCCCACAGTGCAG | 70348 |
rs37144150 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86325059 | TGATTTCTATTTTAG[A/G]CAGACTTTTGCTTTG | 70348 |
rs37145385 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ube2cbp | Mm_Celera | 9:86340190 | AGAGTGACATGTGAC[A/G]TTTCCTCCCTGAAGC | 70348 |
rs37145806 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86375344 | TCCACACAGAAAGAA[A/G]TAGACTCTTGCAACT | 70348 |
rs37147819 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Ube2cbp | Mm_Celera | 9:86333181 | AAAGTCAGAAAAAAG[A/T]AGCCCTTCTAGCTCT | 70348 |
rs37153226 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Ube2cbp | Mm_Celera | 9:86411099 | TCTACCACAGTCCAG[C/T]TGCCTCCGTGGGCAG | 70348 |
rs37153312 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86366922 | ACCCTGATCTCATCT[C/T]AAAATGCTTCAACAG | 70348 |
rs37155019 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86310381 | TGACAGGAAAATCTG[C/T]TTCCAATTTGTTTTA | 70348 |
rs37157096 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Ube2cbp | Mm_Celera | 9:86421584 | ATTATAACAACAAAA[C/G]CAAGAATGCAAATAT | 70348 |
rs37170156 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86309565 | GGGATGTTGCAGAGC[A/G]TCCTAAAATCACAGG | 70348 |
rs37174972 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86333379 | TGATCTGACAATAAA[A/G]AGTTGAGGGCATATT | 70348 |
rs37177099 | snp | A/G | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86312513 | CAGCAAACACAGGGG[A/G]CAAAAACTTACATGG | 70348 |
rs37177642 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86354447 | GACACACAGGCTGCT[C/T]TCTCATTGACTTCTA | 70348 |
rs37181319 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86314375 | GAAGGCATCAGGTAG[A/G]GAATAATCAGAATCC | 70348 |
rs37187246 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86328605 | CTATGTCAAAGACTT[C/T]GTTTGTGCCCAGCAA | 70348 |
rs37191059 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Ube2cbp | Mm_Celera | 9:86423117 | AAAAACACAGGAAGC[A/G]ACAGGAAAACATAGG | 70348 |
rs37191392 | snp | A/T | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86330586 | GTAAATGACCCACAC[A/T]GAGAGGACACTCTCT | 70348 |
rs37202654 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Ube2cbp | Mm_Celera | 9:86358687 | TACTATATGCTAATG[G/T]AATACACAAAGAAAA | 70348 |
rs37213025 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86334097 | GTAACTAGATCATTA[C/T]ATCATTATCTGATTT | 70348 |
rs37231628 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86322584 | GTCTACTTGATTCTA[A/G]TTCACCAGGTGTCCT | 70348 |
rs37232958 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ube2cbp | Mm_Celera | 9:86358713 | GAAAATGAGAGCAAG[C/T]TGATCATGGAAAGAT | 70348 |
rs37237685 | snp | A/T | 0.21875 | 0.248039 | downstream-variant-500B | Ube2cbp | Mm_Celera | 9:86306989 | AGCAGAGATGACTGC[A/T]GATGCCTGTCCTTCT | 70348 |
rs37243709 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Ube2cbp | Mm_Celera | 9:86417607 | CCTTGGAGTATTCTG[C/T]TGGATATAAAATTGC | 70348 |
rs37245217 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86321119 | TATGGATCATAACAC[C/T]GTACCTAGCCTGCTA | 70348 |
rs37248992 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ube2cbp | Mm_Celera | 9:86358786 | TCCTCAGAGGATCTG[A/G]TCTTAGAGAATGAAG | 70348 |
rs37251724 | snp | A/T | 0.497041 | 0.0383476 | intron-variant | Ube2cbp | Mm_Celera | 9:86320091 | GGGTGTTACGCTGGC[A/T]TCCTTTAGTTGGTTC | 70348 |
rs37253640 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86319557 | GGAAGTAAGTGCAGC[A/G]CATGGTCTCATAAAT | 70348 |
rs37255987 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Ube2cbp | Mm_Celera | 9:86374266 | CCCTGTTTGCTGTTA[C/T]TTAATAGCACGTGCA | 70348 |
rs37258992 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86324116 | TTCAAAGATGTTTCG[A/G]ATATGTCAATCAACA | 70348 |
rs37259854 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86308889 | GAAGTTGAGGGAACA[A/G]AAAAGGAAGAAGGGT | 70348 |
rs37269744 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86389596 | ATCTTACAACTTGTT[C/T]AGTTTTTGACAAAAG | 70348 |
rs37272196 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Ube2cbp | Mm_Celera | 9:86389166 | GTTCTTTTATCCAAT[C/T]AGCAATATTAATATA | 70348 |
rs37279135 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86325165 | AAGCACTTTAATCCC[C/T]TGCAGTTATGCTCAT | 70348 |
rs37289478 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ube2cbp | Mm_Celera | 9:86388960 | CATTTACTTTGAAGA[C/T]GCTGTTCTCATCAGT | 70348 |
rs37294190 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Ube2cbp | Mm_Celera | 9:86355278 | CTAAGTGATTTAAAA[C/T]ATGAAACTGGATTTG | 70348 |
rs37305429 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86312075 | ACAGGTGCATTTAAC[A/T]AGACTAAGAAGCGAA | 70348 |
rs37308890 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2cbp | Mm_Celera | 9:86365761 | TGCTGTTTATCTGCA[A/G]AATTCCCAGGCTTCT | 70348 |
rs37315004 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86316456 | GTCTCCAAGTCATGC[C/T]GCATAAGCTCATGCT | 70348 |
rs37315424 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86373671 | CTCAAGCTCTAAAAA[C/T]CTAACTGTATACAGA | 70348 |
rs37336793 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ube2cbp | Mm_Celera | 9:86331698 | AAGTGATGAATTAAA[A/G]GAAATCAACTATAGC | 70348 |
rs37337513 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Ube2cbp | Mm_Celera | 9:86388632 | GGGAAACCAACTGCT[C/T]CTTAAGAATCTGGCT | 70348 |
rs37341442 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86375523 | AAGGTAACCAGACAC[A/G]CATGGGAAAATATTC | 70348 |
rs37343515 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ube2cbp | Mm_Celera | 9:86337272 | CTTTACAAATAATCC[C/T]CTTTGCAGTAACACA | 70348 |
rs37347545 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Ube2cbp | Mm_Celera | 9:86415227 | CATGCATTGGTACAT[A/G]AGTACATTCAGCTGT | 70348 |
rs37357962 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ube2cbp | Mm_Celera | 9:86360286 | TGCTCACAGAGCCTC[A/G]CTCCTTTGTGACAGT | 70348 |
rs37359241 | snp | C/T | 0.18 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86389278 | AAACACTGAAGGTTT[C/T]TACCTAATATTAAAA | 70348 |
rs37361182 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86308568 | CAGAGATAATGCTGA[C/T]GAGAGTGGTGGGTTT | 70348 |
rs37362252 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Ube2cbp | Mm_Celera | 9:86370748 | CCAGAAGTAGGGACC[A/G]CCACCTGATATAAAA | 70348 |
rs37365146 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ube2cbp | Mm_Celera | 9:86325321 | AACTCAGTCTCTCGC[A/G]CGCTTCTAGCCTACA | 70348 |
rs37367276 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ube2cbp | Mm_Celera | 9:86379897 | AAAACCCTTTGTGTC[A/G]TAGAAAATCTCAAAT | 70348 |
rs37372568 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86361219 | CGTCCATCTGAGAAG[G/T]GTCGTCTGCTACTTC | 70348 |
rs37384608 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Ube2cbp | Mm_Celera | 9:86422443 | ATCATAAAAATCTTC[C/T]AATGTTTTATATGGT | 70348 |
rs37385414 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86331675 | CACTAGGTTCCTCCA[G/T]CGTGCCAAAGTGATG | 70348 |
rs37393959 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86320654 | AGAAAGCATGCTGGA[A/G]CATCCAGTGTCTTAG | 70348 |
rs37394509 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Ube2cbp | Mm_Celera | 9:86319727 | TTGTTTCTGAGCTTC[C/G]TATTCATTTCATCAT | 70348 |
rs37395278 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Ube2cbp | Mm_Celera | 9:86365793 | TCTGCATACCTCTAG[A/C]ATACTTGTTTATATT | 70348 |
rs37401095 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86361048 | TAAAGAAAATACAAA[A/C]ACAAAAACTACTAGG | 70348 |
rs37405602 | snp | C/G/T | 0.495868 | 0.0452663 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86413584 | GATAAAATTAGCAAG[C/G/T]TTAAGTCACTATGCC | 70348 |
rs37406828 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86352528 | CAAACACATATGATG[G/T]ACATTGATCCCTACC | 70348 |
rs37417965 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86322491 | CACGTGCAACTGAAT[G/T]CGTGGAAACAACCAA | 70348 |
rs37430184 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86331203 | GTCCTTACTCTTAGC[A/G]TCATTAATGACCTTC | 70348 |
rs37436498 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Ube2cbp | Mm_Celera | 9:86425196 | GAAAATAGAATGATG[C/T]GAACTAGCAGAATTT | 70348 |
rs37437992 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ube2cbp | Mm_Celera | 9:86322309 | CTGAATTTATAATAA[C/T]TAGGCCTTTTGCAAT | 70348 |
rs37450956 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86325874 | CATGCAGAAGAAATG[A/G]CTGCATTTAGAAGTC | 70348 |
rs37451051 | snp | A/C | 0.297521 | 0.245442 | intron-variant | Ube2cbp | Mm_Celera | 9:86419467 | GAGCGCAATGTTGCT[A/C]GAAAGAACGAAGATT | 70348 |
rs37454446 | snp | C/T | 0.497778 | 0.0332592 | utr-variant-3-prime | Ube2cbp | Mm_Celera | 9:86307806 | GCTTGGGCTGGGTTC[C/T]GAGCTGGAGAGCTGT | 70348 |
rs37454614 | snp | A/T | 0.197531 | 0.244432 | intron-variant | Ube2cbp | Mm_Celera | 9:86388309 | ACACACACACACACG[A/T]GAGGAGAAGTACTTG | 70348 |
rs37457184 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86379813 | TAATTGGAGTGATTT[C/T]ACTGAGAACATAAAA | 70348 |
rs37463493 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86310773 | TAAACAGAACTAGAC[A/G]GATGGAGTGGTGAAC | 70348 |
rs37466822 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Ube2cbp | Mm_Celera | 9:86397435 | AAAGCAGACTAGAAC[A/C]ATTACTGTACCTAAA | 70348 |
rs37467496 | snp | A/C/G | 0.489796 | 0.070696 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86331586 | TCTGTCTTCATTCCT[A/C/G]CTAAATGAGTTCGTT | 70348 |
rs37476223 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86419719 | ACTAATGTCCTCAAA[C/T]GACAGAAAATAGATG | 70348 |
rs37482638 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86362316 | TTCTCCTAGTCTTCC[C/T]TGTCCGCATGTCATA | 70348 |
rs37483274 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86314603 | AATATCACCATAAAT[A/G]TCTATAAAATCACTG | 70348 |
rs37483835 | snp | G/T | 0.42 | 0.183303 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86410565 | TTCTGCAACTAACAG[G/T]TAAACAGAGGGAAGG | 70348 |
rs37485919 | snp | C/T | 0.18 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86380100 | ACAGGAAAGCTCTTT[C/T]GCACGTGTGCAAACC | 70348 |
rs37487012 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86316384 | AAGAATGTTCTCAAA[A/G]TCCCAGTGGCTAGCT | 70348 |
rs37495417 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Ube2cbp | Mm_Celera | 9:86319701 | CACATGGCTGGTGTG[A/C]GATCAAGTCTTTGTT | 70348 |
rs37499504 | snp | C/T | 0.18 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86409938 | ACTCTAAAGTGCCGC[C/T]ATCTCCATACAGATA | 70348 |
rs37508948 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86326042 | TACCCCAAAGAAAAC[C/T]GAGGGAGTTCTGAAT | 70348 |
rs37534020 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Ube2cbp | Mm_Celera | 9:86336559 | GAACTGCTCCCAAGC[G/T]TCAGTGACCTCGTAT | 70348 |
rs37534935 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Ube2cbp | Mm_Celera | 9:86366087 | TTAACTGTTTAAGGC[A/G]ATACAAGGCAAACTA | 70348 |
rs37538704 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Ube2cbp | Mm_Celera | 9:86319928 | GCAGAGCCTAAGTGG[A/G]AAACTAAAGCCCCAC | 70348 |
rs37546047 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Ube2cbp | Mm_Celera | 9:86308112 | TAATTGACAGTAAAG[C/T]TAGATATCCATGACG | 70348 |
rs37572058 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86333162 | TGGATACAAAGAACT[A/G]AGAAAAGTCAGAAAA | 70348 |
rs37572486 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86411370 | CAGGTCCTAGCACTC[A/G]AGCTTGGCATTTCAT | 70348 |
rs37584782 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2cbp | Mm_Celera | 9:86357775 | TCTGCCAAACACTTA[C/T]ACAGATAGGGAGAGT | 70348 |
rs37585338 | snp | G/T | 0.495868 | 0.0452663 | intron-variant | Ube2cbp | Mm_Celera | 9:86358363 | TAAAACAAGGTAAGC[G/T]CGCAACCTGAAAATT | 70348 |
rs37597187 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Ube2cbp | Mm_Celera | 9:86380649 | CCAATGACACTTCCA[A/G]TGAAAAGAACAAATA | 70348 |
rs37603345 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86358308 | CTAGCTACAAGTCTC[A/G]GCAACACTGATGGAA | 70348 |
rs37619560 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Ube2cbp | Mm_Celera | 9:86372514 | TAACTTTCATAAATG[C/T]CTGGTCGGAATTATT | 70348 |
rs37628095 | snp | A/G/T | 0.473373 | 0.11227 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86329215 | AGAGACCCGGGAGAC[A/G/T]ATACCAGAGTGTCAG | 70348 |
rs37633586 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86415727 | GTCCAAGATGAATTG[A/G]TCACTATCCAGGAAT | 70348 |
rs37637026 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86324062 | TTTTACTCAAATTCC[C/T]GCCATAGGTCAGTTT | 70348 |
rs37653882 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Ube2cbp | Mm_Celera | 9:86370851 | GTACCTCTCTCCATA[A/G]AAAGAGATGGTCATA | 70348 |
rs37660565 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86328020 | TGATTCCTTCAATGC[G/T]TTGGCCTTCTCTCCA | 70348 |
rs37664959 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ube2cbp | Mm_Celera | 9:86376889 | GCCTCTTATTTCAAT[C/T]ACATTAATTCATAGA | 70348 |
rs37675093 | snp | A/T | 0.497041 | 0.0383476 | intron-variant | Ube2cbp | Mm_Celera | 9:86390669 | AACTCGGTGGAAGAG[A/T]GGAAGAACTCGGTGA | 70348 |
rs37675491 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ube2cbp | Mm_Celera | 9:86366888 | CTTCAGCTTTGAATG[C/T]TCATAGCACCCTGGA | 70348 |
rs37683640 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86359649 | ATTCCAGTGTAGTTT[C/T]TAAATTAAGAGAAAA | 70348 |
rs37719059 | snp | G/T | 0.46281 | 0.131194 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86378908 | GACCAAAAAGTCCAT[G/T]GAAGGCCTGAAGACA | 70348 |
rs37719240 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ube2cbp | Mm_Celera | 9:86309648 | CAGGATCTGTTTGCT[A/G]GACCAGATCTCTCAT | 70348 |
rs37722026 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86333681 | ACTCTTACAGATTCA[C/G]TTAAAAGCTTCAGAA | 70348 |
rs37730509 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86322097 | TGGCCTATATTACCA[C/T]CTGCTTGCAAAATAG | 70348 |
rs37744398 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86389098 | AGTTCCTGCAAGAAA[A/G]TGAAGGGACTACACA | 70348 |
rs37762151 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Ube2cbp | Mm_Celera | 9:86362955 | AGAGCAACCCCCAGT[G/T]CCATCAGATCTACAT | 70348 |
rs37782705 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Ube2cbp | Mm_Celera | 9:86380701 | CAATGAATTCCCAAC[C/T]ACCCAGCAGAAACAG | 70348 |
rs37784372 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Ube2cbp | Mm_Celera | 9:86366978 | CATCCTTGATCAACC[G/T]TAACTAATCATCTAG | 70348 |
rs37797514 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86309801 | TTATGACTCTACTTG[A/C]CCTGGGCACAGCCTT | 70348 |
rs37805770 | snp | A/C | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86323789 | CACACGGAACCTCAG[A/C]TTCAGTTATCTGAGC | 70348 |
rs37822054 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Ube2cbp | Mm_Celera | 9:86389240 | ACTGCAATGAAAACT[G/T]ATTTCTGAGTGTTAA | 70348 |
rs37824315 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86308751 | GGTGCAGGAGGCACG[A/G]GCTTTATGGAGAGGG | 70348 |
rs37827186 | snp | G/T | 0.197531 | 0.244432 | intron-variant | Ube2cbp | Mm_Celera | 9:86409355 | TTTCTTAACTCAAAA[G/T]GCCTCCTTGTCTATC | 70348 |
rs37834812 | snp | C/G | 0.473373 | 0.11227 | utr-variant-3-prime | Ube2cbp | Mm_Celera | 9:86307772 | CCCCAGCAGGTTGTG[C/G]TCACAGAGCAAACTG | 70348 |
rs37841753 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Ube2cbp | Mm_Celera | 9:86374587 | ATACTAGAAATGTTC[C/T]CCCCTTACAATATGT | 70348 |
rs37849788 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Ube2cbp | Mm_Celera | 9:86357948 | AAATTCTAACCATTA[C/T]CATGGACTGGACACT | 70348 |
rs37869698 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86365292 | TTATAAACAATAATG[A/G]CAGGCTCGGGAGAAG | 70348 |
rs37878285 | snp | C/G | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86396842 | GTGAGCCAAGAAGCC[C/G]AATGAGAGACAGGAG | 70348 |
rs37887770 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Ube2cbp | Mm_Celera | 9:86329792 | TTTCCTGCTGGAAAC[A/G]TAGATTTAAAGACAC | 70348 |
rs37894341 | snp | G/T | 0.165289 | 0.235211 | intron-variant | Ube2cbp | Mm_Celera | 9:86371036 | TACCTACATTCATGT[G/T]TCTCAACTCACAATA | 70348 |
rs37921184 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86353382 | GCTGGGCGGTCACCA[C/T]AGGCTACTTCTTGCT | 70348 |
rs37927789 | snp | C/T | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86320217 | TCTGTTATGTATAAG[C/T]ATCATGACCATCAAC | 70348 |
rs37939037 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Ube2cbp | Mm_Celera | 9:86380677 | ATAGTAGTAGCTAAA[C/T]AACACCATCAATGAA | 70348 |
rs37951839 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Ube2cbp | Mm_Celera | 9:86311850 | TGCTGGAGGAAAACT[C/T]ATCCCCTGAGTTATG | 70348 |
rs37968550 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2cbp | Mm_Celera | 9:86357885 | TTATATAAAGGTGAT[A/G]GCAGATGAAATGGAA | 70348 |
rs37974358 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ube2cbp | Mm_Celera | 9:86380728 | ACAGACTGGAGAAGC[C/T]GAGCCAGTTTGCAAC | 70348 |
rs37974881 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86323217 | CCGAACAAAAACAAT[C/T]GCTCCATTGAGGTTG | 70348 |
rs37985860 | snp | A/T | 0.32 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86375512 | CTTGAATTAAAAAGG[A/T]AACCAGACACACATG | 70348 |
rs37992051 | snp | A/G/T | 0.277778 | 0.248452 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86366160 | GCAGGTAAAGAGGTA[A/G/T]CTGGGTGTGAGGATT | 70348 |
rs38008187 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86317200 | GCAAGGTCAAGACCA[A/G]CTGTGCTATATAGCA | 70348 |
rs38016218 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86310612 | GACATCGGGAGAGCG[A/G]ACTCTTTCCTGTGAC | 70348 |
rs38029519 | snp | C/T | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86361394 | ACATACATGCACATG[C/T]ACACAAAACAATTGC | 70348 |
rs38039654 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86374124 | CAGAGCTAAACTTCC[A/G]GTCCTGTATAGCACT | 70348 |
rs38043115 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86339206 | TACTATGCACAAGGG[C/T]TGGGCTACATAACTG | 70348 |
rs38060516 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86330562 | TGGAGGTGTCCCACA[A/G]CAACCTTGGTAAATG | 70348 |
rs38067649 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Ube2cbp | Mm_Celera | 9:86369887 | ATTTGCACCAAAAAC[C/G]ACACGTTATAATACA | 70348 |
rs38103638 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Ube2cbp | Mm_Celera | 9:86409550 | CATACCAGTAGAAAA[C/T]CATGCCTTCAGCCTA | 70348 |
rs38110289 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Ube2cbp | Mm_Celera | 9:86421881 | TGGAGAGGGAGATAA[C/G]TTTCATAGTTTATAC | 70348 |
rs38113264 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86323204 | AATTGCTAAAAGACC[A/G]AACAAAAACAATTGC | 70348 |
rs38130679 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86326287 | CAGACGCCTTGCAAA[C/T]GAAGAGAAACCCAAA | 70348 |
rs38148160 | snp | G/T | 0.21875 | 0.248039 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86355691 | AGGGCTCCTGAAGAC[G/T]GTCACCAACAGTGTG | 70348 |
rs38162188 | snp | C/T | 0.18 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86416873 | ATGTGTGGAAGTGAT[C/T]TTAAGGAAGTTTTGT | 70348 |
rs38165278 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Ube2cbp | Mm_Celera | 9:86308981 | TTCTGTGAAGATCAA[A/G]TGAGATAATAGGCCG | 70348 |
rs38179078 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Ube2cbp | Mm_Celera | 9:86357848 | CCCAGAAATGACACT[A/G]TTGTCACTGTCTTGG | 70348 |
rs38194924 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ube2cbp | Mm_Celera | 9:86321821 | CTTTTTTTTTCTGTC[C/T]GCTATTTGTGAATGA | 70348 |
rs38199938 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ube2cbp | Mm_Celera | 9:86363239 | TCTGTGTTCTGCTCA[A/G]CATCTGCTTATTTCC | 70348 |
rs38201839 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ube2cbp | Mm_Celera | 9:86413843 | AAGTGTCAACTTTCA[A/C]AAGAATTCCTTATAG | 70348 |
rs38201842 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86366147 | ATAAATATTAATAGC[A/G]GGTAAAGAGGTAGCT | 70348 |
rs38245088 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ube2cbp | Mm_Celera | 9:86307968 | ATCTGGTCAACAGGA[C/T]ACAGACCAACCTCAG | 70348 |
rs38251940 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86340813 | AAATGCCTTGATATT[G/T]TAAGTATGGTGTATA | 70348 |
rs38262839 | snp | A/T | 0.197531 | 0.244432 | intron-variant | Ube2cbp | Mm_Celera | 9:86367271 | TCTGATGCATTACCA[A/T]AAGATGGAATAAATA | 70348 |
rs38263192 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86319200 | AATTGTTTTCCTTTT[G/T]GATGAAACTGAGTGT | 70348 |
rs38267635 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86361070 | ACTACTAGGAAGTTT[C/G]AAAGTCACATATACT | 70348 |
rs38274211 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86335834 | AGCTTGGCAGCACTC[C/T]AAACACTCTCTGTAA | 70348 |
rs38274822 | snp | C/G | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86323054 | AAGAACGTCCTGGCA[C/G]AGGCACAGAAACAAA | 70348 |
rs38289033 | snp | A/G | 0.5 | 0 | intron-variant | Ube2cbp | Mm_Celera | 9:86375584 | AGAAATAGATTAGAA[A/G]ACAGTATAACACAGT | 70348 |
rs38300526 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Ube2cbp | Mm_Celera | 9:86376940 | AAATAAAAGTGGTAG[C/T]TTAGGAGAAAAAGAG | 70348 |
rs38310307 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86316705 | CTTGGCTCTGTGCAC[A/T]TGGCATTTCAGGGTA | 70348 |
rs38321522 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86338877 | CCTCACATTACATGC[A/G]GCTGGTTGTAGGGTC | 70348 |
rs38324263 | snp | C/G | 0.345679 | 0.230967 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86410751 | CACAGTCAGTGACTT[C/G]AGGACAGTCTGCAAG | 70348 |
rs38330064 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Ube2cbp | Mm_Celera | 9:86331715 | AAATCAACTATAGCA[C/T]CAAGCATATAACTGA | 70348 |
rs38333765 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86359835 | CAATAATCACACCTT[C/G]TGTTTTCTATGATCT | 70348 |
rs38379850 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ube2cbp | Mm_Celera | 9:86364827 | GAAAAGTCTCTAAGT[A/G]TACTGACAAGCACCC | 70348 |
rs38388552 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86340380 | ACCAGAAACAAATGA[A/G]GAAAAACTATACCCC | 70348 |
rs38392615 | snp | G/T | 0.497041 | 0.0383476 | intron-variant | Ube2cbp | Mm_Celera | 9:86359228 | AAACCAACAATGACT[G/T]TGCTTTCAAGAGAAA | 70348 |
rs38406020 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86323102 | AACAGGGACTGTAAC[A/G]TGGTTAAGGGATGGA | 70348 |
rs38406465 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86320180 | TTATTTTCTTTAGCC[A/G]ACTGTGGAGAGCGAA | 70348 |
rs38456493 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86339621 | GAAGTAACTAATAGG[A/C]CAAATTCTTGACCAA | 70348 |
rs38468520 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2cbp | Mm_Celera | 9:86373422 | AGACAGTGGTAAGGC[C/T]GTGTCTAGAATCCTG | 70348 |
rs38481845 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ube2cbp | Mm_Celera | 9:86332699 | ACCATCTATGCTCAC[A/G]TTGTACATGTATAAT | 70348 |
rs38543117 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86317339 | GATGTGCACAGAAAA[C/T]CTTGTACAATCTTAA | 70348 |
rs38550299 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86326694 | ACAGAAGACAAAAGG[C/T]ACTGACAAAAGCCAA | 70348 |
rs38552364 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2cbp | Mm_Celera | 9:86313584 | CATTTACCATATATA[C/T]CCAGTCACTTCTATA | 70348 |
rs38558165 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Ube2cbp | Mm_Celera | 9:86317062 | AAAGGAAGTGTCATG[C/T]CTCACACACACACAC | 70348 |
rs38560028 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Ube2cbp | Mm_Celera | 9:86415248 | ATTCAGCTGTCAGGA[A/G]AGCAAACAGCCTGTT | 70348 |
rs38581980 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Ube2cbp | Mm_Celera | 9:86378511 | CATGTAAATGCATGT[C/T]CCTAATACATTTTAA | 70348 |
rs38586512 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86320010 | TACATGATGAGTGCC[A/T]ACAAGACAGTGGGAA | 70348 |
rs38593643 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2cbp | Mm_Celera | 9:86363091 | TAAGATGGCCAGTTG[C/T]GAAGAGATGGGCAAG | 70348 |
rs38602788 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86364884 | GATGAAGGTTTAGGC[A/G]AGAATGAAAGTGAGC | 70348 |
rs38643971 | snp | A/T | 0.486111 | 0.0821678 | intron-variant | Ube2cbp | Mm_Celera | 9:86321383 | TAGTGTTTAAAGAGT[A/T]AGCTTACCCCTACCA | 70348 |
rs38649600 | snp | C/G/T | 0.18 | 0.24 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86363255 | CATCTGCTTATTTCC[C/G/T]CAAACCACAGAAAAC | 70348 |
rs38685137 | snp | A/G/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86362177 | TGCAATGTAGATAAC[A/G/T]AGGGCTCCTGGTTCT | 70348 |
rs38695419 | snp | C/T | 0.18 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86368862 | TGCCTCTAGTACAGC[C/T]TTCCTGATTTCTATA | 70348 |
rs38713238 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Ube2cbp | Mm_Celera | 9:86319194 | AAAGAGAATTGTTTT[C/G]CTTTTGGATGAAACT | 70348 |
rs38714963 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Ube2cbp | Mm_Celera | 9:86327891 | ACAGTGATACCAGAA[C/T]ACATTCTCTGCTGAG | 70348 |
rs38731379 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ube2cbp | Mm_Celera | 9:86380609 | TTCTGACTGAAGGTG[C/T]CCCAGATGGAGCAGA | 70348 |
rs38733782 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Ube2cbp | Mm_Celera | 9:86373222 | CCACACAAATAAAAG[C/T]CAAGATGCCGTTTGA | 70348 |
rs38742859 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2cbp | Mm_Celera | 9:86364875 | GACTCGGAGGATGAA[A/G]GTTTAGGCAAGAATG | 70348 |
rs38798924 | snp | A/G | 0.42 | 0.183303 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86373737 | TGAGTGCATAAGGGG[A/G]CACGGACATTGTGCA | 70348 |
rs38804873 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86361119 | TAGAGTCAAAGATAC[A/G]AAACCCAGTGTGGAA | 70348 |
rs38807581 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86337175 | AACATGAGAGGAAGG[C/T]GATAGACAGAAGCAA | 70348 |
rs38811095 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86395597 | AAGAAGCTAACCAGG[A/G]CCTAGTGATAAAACA | 70348 |
rs38829108 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86403357 | ACATGCTGGCCATAC[A/G]GAAAGAATGGAAACC | 70348 |
rs38830211 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86327988 | ATTCAGAAACGCCTT[C/T]GGGAGACATGCTGCA | 70348 |
rs38845119 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Ube2cbp | Mm_Celera | 9:86358407 | AAAACCAATCTTAAG[C/T]CAGTCCCCAAATCTT | 70348 |
rs38916547 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ube2cbp | Mm_Celera | 9:86319060 | ATTTTCCCAATGGGA[C/T]GTACAAACTGGCACT | 70348 |
rs38923282 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86418825 | TGCTTATATTCTACC[A/G]TTTACTCGGCTTAAC | 70348 |
rs38936189 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86338220 | ATGGTAGGAACAGAA[C/T]TCCAATGGCTTAAAA | 70348 |
rs38966329 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ube2cbp | Mm_Celera | 9:86370563 | CCCTTAAAGGGTGAA[A/G]GTAAAAAAAATATCA | 70348 |
rs38966374 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2cbp | Mm_Celera | 9:86329970 | CATGTAATATGTCAT[C/T]CCAGCTAACAACTCA | 70348 |
rs38970039 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86362991 | CTATGGAAGGCCATG[A/G]CACTCCAACTTTTTC | 70348 |
rs39020343 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86319502 | TTTTAAAAAACAGTT[C/T]GTATAAGCCCTTTGC | 70348 |
rs39032608 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Ube2cbp | Mm_Celera | 9:86413519 | TAACAAACTGTCAGC[C/T]GTGCTTCCCAATTGC | 70348 |
rs39118017 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86316577 | TAGAAGATGCATACC[C/T]GTCCCTGTGATGCCC | 70348 |
rs39122464 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86335234 | ATATGTAAGACCAAC[A/G]GAAACACAACAGACA | 70348 |
rs39151048 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86320501 | CTCAGGTAGGGTGAT[G/T]GAAACATAGGAGGAA | 70348 |
rs39176497 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86328235 | GTCTCTAACCTTCAT[A/G]TTGAATCTCCGGGAC | 70348 |
rs39200737 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86338423 | GAGTTCCACACTTGA[A/G]CTTAGGGAAGACTTT | 70348 |
rs39205438 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86313872 | AGCATGGTAGTTCTT[C/G]GGTTCTGCCTCTGGA | 70348 |
rs39207410 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86316553 | TTCCACCTTTCAAAA[C/T]AGCATCAATAGAAGA | 70348 |
rs39236918 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ube2cbp | Mm_Celera | 9:86374863 | CACGGCGATTGGCCG[A/G]GTCCTGCTGCACTCT | 70348 |
rs39250172 | snp | A/T | 0.497778 | 0.0332592 | utr-variant-3-prime | Ube2cbp | Mm_Celera | 9:86307734 | TCAGCACAGTCCCCA[A/T]TCTGCAGCTTAGTTC | 70348 |
rs39255030 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86341191 | AGCATTAGGAAAGAT[C/T]GTTAGGAAAGAAAAG | 70348 |
rs39266621 | snp | A/T | 0.473373 | 0.11227 | intron-variant | Ube2cbp | Mm_Celera | 9:86328560 | GAAGGACAGGCTGGG[A/T]GCTGGGTGCACATCA | 70348 |
rs39318010 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86338379 | AGATTGCTGTGGACC[C/T]GCAGGACAGACAAGC | 70348 |
rs39372660 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86373772 | AGTAGTACTTAGTTC[C/T]AGCACCAAGCAGATG | 70348 |
rs39404393 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86328095 | GGTATTCTGACCTGC[C/T]TGCTTTCCCTCTAAT | 70348 |
rs39433861 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Ube2cbp | Mm_Celera | 9:86361402 | GCACATGTACACAAA[A/G]CAATTGCGTAATCTA | 70348 |
rs39484483 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86373682 | AAAATCTAACTGTAT[A/G]CAGATCTGTGGTAAC | 70348 |
rs39517434 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ube2cbp | Mm_Celera | 9:86359537 | GAACTGCTGTTATAA[A/G]GTCTTATCGTGATGA | 70348 |
rs39523115 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86365139 | AGAAATAAGCAGAGG[A/G]AAATGCCAAAAACTG | 70348 |
rs39551515 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86322333 | TTGCAATTATATCCA[A/G]TTCATGCCATAGGAT | 70348 |
rs39613166 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86315785 | ACTAAGAGTTAAGTA[A/C]ATGAGGTTTTGGTGG | 70348 |
rs39699241 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2cbp | Mm_Celera | 9:86313536 | CATTACTCAGAGATA[C/T]TAAATAATGTTTTGT | 70348 |
rs39791699 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86336532 | CATTATATAGCCTTG[C/G]CAAAGCCTCCTGAAC | 70348 |
rs39940239 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86309529 | GAGGGTGTGGTGACT[A/G]ACATCTAACAGGGAG | 70348 |
rs39987789 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86380273 | AACATTTTTTTTTTT[C/T]CACTGATTGACACAC | 70348 |
rs45645062 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86352385 | AAATAACCAGATTTT[C/T]CTCAGGTAAATATAA | 70348 |
rs45654327 | snp | A/T | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86363945 | AAACACATACTGTGG[A/T]GGTAATCAACAGCCT | 70348 |
rs45657512 | snp | G/T | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86445895 | GGCTGGGAGGAGGCC[G/T]GCATTCCTCATCTTA | 70348 |
rs45695464 | snp | A/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86441234 | GCAGACCTGTGCCCC[A/G]AGAAGACACACACAG | 70348 |
rs45700924 | snp | A/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86406976 | AGAAGTCACTGTCAC[A/G]TGGCTTTGTTCTGTA | 70348 |
rs45704962 | snp | A/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86332032 | ACTCTTGATGAAGGA[A/G]TATAAATATGACCCC | 70348 |
rs45710686 | snp | G/T | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86443061 | AAGGGTTTTTACCCA[G/T]GGCTTTCTGGCTCTA | 70348 |
rs45712579 | snp | A/G | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86348310 | TTCCGGGACTCCGCG[A/G]AGGGCAGTAAAAAAA | 70348 |
rs45712873 | snp | A/G | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86457270 | GGGTGTGTATGGGGT[A/G]GAGGGTGGGGTCACA | 70348 |
rs45719454 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86450926 | ACGAAGCATCAACAC[A/G]GTTCCTTCCAATGCT | 70348 |
rs45752914 | snp | A/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86357611 | GAATATGTAATACTG[A/G]TAGGAAACGCATATC | 70348 |
rs45756813 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86429102 | TTCAAATCTCCATTA[C/T]GGCTGCTTCTTTGAA | 70348 |
rs45767209 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86363718 | ATAAATCAGTATTGC[C/T]AAAGACATTATGCAC | 70348 |
rs45778572 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86398867 | TACCTGAGATTCTCT[C/T]TTCTTATCTCTTGTA | 70348 |
rs45787056 | snp | A/G | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86440953 | GAGAAGTCTCCCTTT[A/G]CTCCCTACTCGAAAA | 70348 |
rs45789945 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86439353 | ATACACACAACCACA[C/T]ATATATATGTGTGTG | 70348 |
rs45821031 | snp | A/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86452414 | CGCCCCAAACAACAG[A/G]AAAAAAAAAAAAGCC | 70348 |
rs45824142 | snp | G/T | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86449300 | AGGAACGCAAAGCTC[G/T]GTAGAGTGTCCTCAC | 70348 |
rs45833116 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86354772 | CACTTTCCCTCTCTC[C/T]CTTCTTTCCTTCCTT | 70348 |
rs45833361 | snp | A/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86384158 | TGTTTTTCCTTGAAC[A/T]CAAATTTGTATCAAG | 70348 |
rs45838875 | snp | A/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86352584 | TTAAGGCTTGTGACA[A/G]GAAAGGGTCACTTAA | 70348 |
rs45846572 | snp | A/T | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86456063 | CACAGGTGAAGACAG[A/T]ACAAACAAGACAATG | 70348 |
rs45847808 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86439504 | GGCACTAAGAACCCG[A/T]AGCTGACAGCAATCT | 70348 |
rs45858903 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86448312 | TCCACAGGGTAATTA[C/T]GGCACATCACCAGTG | 70348 |
rs45873016 | snp | A/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86436106 | TATTTAGTTAGAATC[A/G]CAACATTTATAAAGC | 70348 |
rs45875050 | snp | A/C | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86317434 | TTAATAATCAGCAAC[A/C]AAAATCTACAAATCA | 70348 |
rs45896087 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86443428 | GGAGATCTCCAAGTA[A/C]ACTTGACGCCACCTG | 70348 |
rs45899137 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86452105 | GCATAGAGACCCTAA[A/C]ATCCTTGTCCCAGGA | 70348 |
rs45907406 | snp | A/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86334737 | TGAGAAGTAGTCAGG[A/T]TTTAAAGAATATGAG | 70348 |
rs45907882 | snp | C/T | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86454357 | CTTTTAACCATGATC[C/T]GCCCCTCACCGTTTC | 70348 |
rs45919190 | snp | A/C | | | intron-variant | Ube2cbp | Mm_Celera | 9:86320313 | AAGACATACAGATCA[A/C]CAATGGCTGCTGAGC | 70348 |
rs45934650 | snp | G/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86323958 | TGTATTTATACTTGC[G/T]TAGCATGCGCAAAGC | 70348 |
rs45936619 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86378948 | AGCAGAGTGCTGCCT[C/T]GTACACTTGAACGCC | 70348 |
rs45941748 | snp | A/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86366474 | GGGCAGAAAAGAGGG[A/G]CTGGAACAAAGGTTC | 70348 |
rs45943827 | snp | C/T | 0.42 | 0.183303 | intron-variant | Ube2cbp | Mm_Celera | 9:86435631 | GCAAGCACTTCATCC[C/T]TCTAAAGAGTGGGCA | 70348 |
rs45946667 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86452361 | GTTCTCCACCAGCCT[A/G]GGACCCACAGTGAGA | 70348 |
rs45951011 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Ube2cbp | Mm_Celera | 9:86428946 | AGTCACTTTCTTCTA[G/T]CTGGGTACAGTTAGA | 70348 |
rs45964940 | snp | C/T | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86355558 | ATTGTAGAATAGCTG[C/T]CACCTACAAGTGTGT | 70348 |
rs45968713 | snp | A/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86354587 | TTTATTGGCATGCTC[A/G]TCATGCTTAATCACT | 70348 |
rs45970144 | snp | C/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86368914 | CTGCATGCTACCTGT[C/G]CATGCCTCCACCCAT | 70348 |
rs45977934 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86351152 | TTATTTCAAAACCGA[C/T]ACTCATCAACCATTA | 70348 |
rs46001053 | snp | A/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86365426 | GAAGCAGCCATCTTG[A/G]AGGAGACCTGGAGCT | 70348 |
rs46003527 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86427890 | CTGACTTTCTGTTTA[C/T]TTTGTTGTTTATAAA | 70348 |
rs46007155 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86445963 | CCCCAAAGAGACATT[C/T]AACTAGACAATTTGC | 70348 |
rs46007456 | snp | A/C | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86422436 | CACAGAAATCATAAA[A/C]ATCTTCTAATGTTTT | 70348 |
rs46012445 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86439032 | CTAAATATAAGACCC[C/T]TCCTTTAATATACAA | 70348 |
rs46019201 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86375615 | GGTTTTCAATCTTCC[C/T]AATGCTGAGACCCTT | 70348 |
rs46021351 | snp | A/T | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86413271 | CAAAGAAATGTAGAC[A/T]AAACGGTATACTGTG | 70348 |
rs46034769 | snp | A/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86414966 | GTAGGGGAAAAACAG[A/G]AGGATACAGAGCCCT | 70348 |
rs46041380 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86436150 | CAAGTTCCAGACTAC[C/T]TTGGTTAACACAATG | 70348 |
rs46052689 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Ube2cbp | Mm_Celera | 9:86429267 | TGGAAGTCATTGTGC[C/T]TCTTGAATCTGTAGA | 70348 |
rs46068587 | snp | A/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86318772 | TACTGAGCCATCTCT[A/G]TAGCCCCAAAAGGCA | 70348 |
rs46070091 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ube2cbp | Mm_Celera | 9:86438687 | GCATTCATACACACA[A/C]AGAAAGAAAATGTTT | 70348 |
rs46070474 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86438979 | CCTTGTCATGACAGC[C/T]ACTTCCCATAGTCCC | 70348 |
rs46083370 | snp | A/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86428684 | TGATAAAAACATGCA[A/G]TGATTATTAAATGTT | 70348 |
rs46097502 | snp | A/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86357089 | GACTAGTACTTAACT[A/T]AACATTGATTATCTG | 70348 |
rs46098700 | snp | A/T | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86321612 | TCCCTGCCATGCCTA[A/T]CACCTCCTAGCTTCT | 70348 |
rs46100167 | snp | A/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86446061 | TTCCAGAGGTCCTAA[A/G]TTCAATTCCCAGCAA | 70348 |
rs46100565 | snp | G/T | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86319252 | ACTATTAACAGGGTT[G/T]TTTTTTTTCTAATTT | 70348 |
rs46101268 | snp | A/T | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86378061 | GGGAGTCATAGAATC[A/T]TGACTATAAACCTGT | 70348 |
rs46103034 | snp | A/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86363513 | CATAAATAGTTTAAA[A/T]TGAATTTTGTAATCA | 70348 |
rs46110569 | snp | C/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86457639 | AAACATCCACAAATT[C/G]ACAGGGCTTTAGATT | 70348 |
rs46113921 | snp | G/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86357448 | TAGAGGGCTTGAAAT[G/T]ACTTATATAAATTTA | 70348 |
rs46123067 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86325527 | AAAACACCTGGCTAC[C/T]ACTGTTCTTGCCTCC | 70348 |
rs46129222 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, intron-variant | Ube2cbp | Mm_Celera | 9:86451944 | GGTGCAGCCGTCAGG[A/G]GTTCTCACCAAAAGA | 70348 |
rs46132696 | snp | A/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86386834 | ATGTACATTACACCA[A/T]TATTCTCTAAGAAAC | 70348 |
rs46133224 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86454624 | TGTTACCTCTCATTT[A/G]AATAAAAGACTTATT | 70348 |
rs46140144 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86441982 | TGGAAAAAGCAACCG[C/T]TCCCTTCTCAACCAT | 70348 |
rs46153633 | snp | A/T | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86444914 | TGTCTTGTTAAAAAA[A/T]AAATAAAAAAGGTGT | 70348 |
rs46175604 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86453040 | TTGCAGCATGTAGAG[A/G]GGAGAAGAGGGAACA | 70348 |
rs46194660 | snp | C/T | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86452733 | ACTGCTTAGGAGATC[C/T]CAGCGCGGGAGGAAA | 70348 |
rs46197306 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86446673 | TTCTTCTGTCATAGC[A/G]CCAACCAAGAATGTA | 70348 |
rs46227124 | snp | A/G/T | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86452508 | TGCAGTATTTTTGAA[A/G/T]CACAGTTGGCACCTA | 70348 |
rs46234811 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86451670 | GAGTGATACAGCACA[C/G]AGCACACAGCTGCTA | 70348 |
rs46237872 | snp | A/G | | | upstream-variant-2KB | Ube2cbp, Dopey1 | GRCm38.p3 | 9:86465897 | tccccatagaaccga[A/G]gatcaccgacccagg | 70348 |
rs46241420 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86448214 | AAATTCAGAGGAAGC[A/G]TTTGTGCCCAAGAAA | 70348 |
rs46243592 | snp | A/G | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86452519 | TGAAGCACAGTTGGC[A/G]CCTAGAAATGTCCCC | 70348 |
rs46255050 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86449553 | AGTTATTAGAAGCGA[A/G]GAATAGAATCCACTT | 70348 |
rs46279400 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86457672 | AAAGCACTGTTTCAA[C/T]TTAGCAACAAGACTA | 70348 |
rs46285136 | snp | G/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86325881 | AAGAAATGACTGCAT[G/T]TAGAAGTCTCACCAG | 70348 |
rs46309288 | snp | A/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86440440 | AGCTGGAGAATGGAA[A/G]GAAGCAGTTAAAAAT | 70348 |
rs46311496 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Ube2cbp | Mm_Celera | 9:86444353 | ATGCAAAGCAGGTGC[G/T]CCATGGTGTAACTAC | 70348 |
rs46318265 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Ube2cbp | Mm_Celera | 9:86448635 | CGTTCCGCTCCAGCA[C/T]CACGGTGAGAGTCGG | 70348 |
rs46327658 | snp | C/T | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86449283 | TCTGTGGAGCAGACC[C/T]AAGGAACGCAAAGCT | 70348 |
rs46330345 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86439339 | ATCTATATTAATACA[C/T]ACACACAACCACATA | 70348 |
rs46345947 | snp | C/T | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86375197 | CAGTCAGAAGGGTCA[C/T]ATGATTGGCCAGCAC | 70348 |
rs46347830 | snp | A/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86352460 | AAGAGCTTTTCCTAT[A/G]TCATAGAAATGGCTC | 70348 |
rs46348616 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86448506 | CTTTCTGTGGAAACC[C/T]TCACACACCCTCAGA | 70348 |
rs46352140 | snp | A/C | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86378891 | AAGGAAAACCTCCCA[A/C]GGACCAAAAAGTCCA | 70348 |
rs46369324 | snp | C/T | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86445568 | GTCAATAATCCTATG[C/T]ACCTTCCTGGGAACG | 70348 |
rs46379199 | snp | A/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86351041 | GCTCTGTGCTTTTCA[A/G]TTTCCATATGAGCCT | 70348 |
rs46385393 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86366433 | CCTCAAGTTATTGGT[C/T]AATAAAGATGCCTAC | 70348 |
rs46389776 | snp | A/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86356592 | AGCAGTCGGGGCCAA[A/T]GCTTTCTTGTCTTTG | 70348 |
rs46390954 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86429547 | CTGAACTGCCAGTGT[C/T]AATTATAAAGAAGTA | 70348 |
rs46404951 | snp | A/G | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86412544 | ATTCCTGTATTGATA[A/G]AGTAGCTGTAGTCCT | 70348 |
rs46410464 | snp | A/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86445980 | ACTAGACAATTTGCT[A/G]GTTTACTAATAAAAG | 70348 |
rs46418407 | snp | C/T | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86320941 | CAATAAGGCCACACC[C/T]TGTAATCTTTCTCAA | 70348 |
rs46471144 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86368246 | CTGGGCAAGTGCATC[C/T]CTCTGGCTCAGCCTG | 70348 |
rs46487768 | snp | A/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86445030 | AGTTACCCTGGTGCT[A/G]AGAATTAAGCCATTA | 70348 |
rs46524541 | snp | C/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86445997 | TTTACTAATAAAAGA[C/G]CATCTAGGGCTAGAG | 70348 |
rs46529685 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86318764 | AACTTAATTACTGAG[C/T]CATCTCTATAGCCCC | 70348 |
rs46533678 | snp | A/C | | | intron-variant | Ube2cbp | Mm_Celera | 9:86355618 | GCATGTCACAGAGGA[A/C]GAAGAGAGAAACATG | 70348 |
rs46535059 | snp | A/G | 0.5 | 0 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86452729 | CTGTACTGCTTAGGA[A/G]ATCTCAGCGCGGGAG | 70348 |
rs46535138 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86350702 | AAAAACAAATGACAT[C/T]CTGAAAAAGGAGAAA | 70348 |
rs46542512 | snp | G/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86385013 | GAGTACATACCATGT[G/T]TGTCTTTCTTGATCT | 70348 |
rs46542999 | snp | A/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86378686 | AGGTCCTAAGTTCAA[A/T]TCCCAGCAACCACAT | 70348 |
rs46554092 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86323982 | GCAAAGCCCCTGACT[C/T]AATCACCCCGTCTAC | 70348 |
rs46573801 | snp | C/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86331840 | CACAAACTATTCCTA[C/G]CTGCAGAAAGTGAGG | 70348 |
rs46578083 | snp | A/C | | | intron-variant | Ube2cbp | Mm_Celera | 9:86308092 | ATCCATTTTTTAAAA[A/C]GTTTTAATTGACAGT | 70348 |
rs46585978 | snp | A/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86446410 | CTCTCTGTCTTCTCA[A/G]TGAGAAAGCCAAAGT | 70348 |
rs46596454 | snp | A/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86351018 | TGGGAGCTAAGGTCT[A/G]TAACAAAGCTCTGTG | 70348 |
rs46598076 | snp | C/T | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86443091 | AAAACCACTCTTTCC[C/T]TTGGAATACCTTTAC | 70348 |
rs46605577 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86452774 | ACATTCAACACAGAT[G/T]TAAGTTTTCTTGTGT | 70348 |
rs46631149 | snp | C/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86328810 | CGGTCTTACATGCAG[C/G]AGGTTTTAGCAAATA | 70348 |
rs46633306 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86441170 | CTGCATACACACATG[A/G]CAGGCCTGTGCCCTG | 70348 |
rs46646357 | snp | C/T | | | downstream-variant-500B | Ube2cbp | GRCm38.p3 | 9:86306818 | AATACCTAATCCCAC[C/T]GCTCTGCTGGGTAAA | 70348 |
rs46647752 | snp | A/T | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86447322 | ATGGTGGATGGAAAC[A/T]CGCCTTGCCACTGCT | 70348 |
rs46658862 | snp | A/G | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86369569 | ATTCTCCTAATAGCG[A/G]AGAAAACAACCAGAA | 70348 |
rs46661131 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86376832 | GGCCCAGGCTTCTCA[C/T]AGTCAACCAGCCCCA | 70348 |
rs46662689 | snp | A/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86359341 | AGCGATTCCTGGCCT[A/T]TGTAATGCAGTGGCA | 70348 |
rs46671709 | snp | A/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86362849 | ATGGATGAACCACAC[A/T]CATACTCCAAACAAA | 70348 |
rs46682342 | snp | G/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86323726 | AATAGTAGGGGAGGG[G/T]CAGTGGGTACCAATC | 70348 |
rs46684567 | snp | C/G | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86373459 | AAGTTCTCCAATTAA[C/G]GAGAAACCCCAGGGG | 70348 |
rs46686388 | snp | C/T | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86447507 | ACATCACAAGACAAG[C/T]GAATGCTATGTCAGC | 70348 |
rs46690445 | snp | G/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86329502 | CCCAGCACTTGGAAG[G/T]CAGAAGTAGGCAGAT | 70348 |
rs46700038 | snp | G/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86366571 | TAGGTAGATGGATTG[G/T]GAACCCATGTCCATG | 70348 |
rs46707841 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86370491 | GGGAGCACACTGATG[C/T]CACTGATGAAAGGAT | 70348 |
rs46712919 | snp | A/G | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86454480 | ACTGATACTCTGGGA[A/G]GTCAGACTTTCAACA | 70348 |
rs46720331 | snp | G/T | 0.495868 | 0.0452663 | intron-variant | Ube2cbp | Mm_Celera | 9:86429454 | GCGCTTCAGTGTGCA[G/T]GGTTAAAGATTCTTC | 70348 |
rs46732050 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2cbp | Mm_Celera | 9:86452337 | AGTCAGAGAGTAAAT[A/G]TTTCCTGAGTTCTCC | 70348 |
rs46733844 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86432372 | TCACTCAGGATGATA[C/T]CCTCCAGATACATCC | 70348 |
rs46742900 | snp | A/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86441599 | TCTTAGATTCTCCCA[A/T]TCATCTATGAGTATT | 70348 |
rs46749324 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Ube2cbp | Mm_Celera | 9:86456913 | ATGTTCACAAAAACA[A/G]TGTAGGGAACTGATT | 70348 |
rs46749770 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86447147 | TTACTGCAATAGCTA[C/T]CAGCGAATGGTGAAT | 70348 |
rs46781328 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86325362 | CTTGTTCCAAAAGGA[C/T]TGTGCTCCATCTTAG | 70348 |
rs46786403 | snp | A/C/T | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86334730 | GTAGATATGAGAAGT[A/C/T]GTCAGGTTTTAAAGA | 70348 |
rs46790068 | snp | A/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86379510 | ATAAGAATATACCAA[A/G]ACCACCAAAAACAAA | 70348 |
rs46793298 | snp | A/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86367215 | TGCCAGGCAGTAAGT[A/G]TAACATTTACAAGAT | 70348 |
rs46799309 | snp | G/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86399616 | TTATCCAGCCTGCTA[G/T]TCTATGTCTTTTTGT | 70348 |
rs46806635 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2cbp | Mm_Celera | 9:86439706 | AAACGAAAGCTGTCC[A/G]GCATTGATTTTCTTG | 70348 |
rs46812918 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86332441 | AAAAGATTAAGCTCA[C/T]CCCCAAAGAACTATT | 70348 |
rs46813572 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86368925 | CTGTGCATGCCTCCA[C/T]CCATCCAGTACTTCT | 70348 |
rs46823096 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86437985 | TTTACAAGATGAGAT[C/T]AGGCTGGCTTTGAAC | 70348 |
rs46828775 | snp | C/T | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86350822 | TTGTAGAGCAGTAAA[C/T]TATAGTCTACTAAAA | 70348 |
rs46839038 | snp | A/C | 0.46281 | 0.131194 | intron-variant | Ube2cbp | Mm_Celera | 9:86446374 | TTTGGCTAGAAGAAG[A/C]TAAGGTGGTACAAAC | 70348 |
rs46872258 | snp | A/T | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86446670 | TTTTTCTTCTGTCAT[A/T]GCACCAACCAAGAAT | 70348 |
rs46882315 | snp | A/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86362809 | TAGAGATGATATTTG[A/G]TGTACACACATACAC | 70348 |
rs46893964 | snp | A/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86329427 | TTTTAGGTTCAGTGT[A/G]AGACCTCCTCTTAAA | 70348 |
rs46907660 | snp | A/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86407067 | CAAGGGAGTAATGTC[A/G]GAGAACATGTGAAGA | 70348 |
rs46951783 | snp | A/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86357070 | TTAAATGTCATTCCA[A/T]TAAGACTAGTACTTA | 70348 |
rs46953583 | snp | A/G | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86411712 | TGCCTCCCAGGGGGG[A/G]CATGTTGATTTCTAA | 70348 |
rs46962882 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86432051 | CTCCCTGGAGAATAC[C/T]CACTGCACTAGATAA | 70348 |
rs46983059 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86328800 | CATCCACACACGGTC[C/T]TACATGCAGCAGGTT | 70348 |
rs46995024 | snp | A/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86332424 | GACTGAACTGCTGCC[A/G]AAAAAGATTAAGCTC | 70348 |
rs46995048 | snp | A/G | | | upstream-variant-2KB | Ube2cbp, Dopey1 | Mm_Celera | 9:86466559 | TGCTTGCAACTTCAG[A/G]GCATCTGACCTCTTT | 70348 |
rs46998183 | snp | A/C | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86320328 | ACAATGGCTGCTGAG[A/C]GAGGGAGAGTCAGTC | 70348 |
rs46999725 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Ube2cbp | Mm_Celera | 9:86438536 | GCAAACCTCAAAGAC[A/G]GACACGGTTGAGGAC | 70348 |
rs47010220 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86406795 | GCTCTGTGAGGCTAA[C/T]AGGGCTATGTCCAAG | 70348 |
rs47022836 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86463405 | CATCAGTTGGCTATG[C/T]CAGCTTGACATACGT | 70348 |
rs47026128 | snp | C/T | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86321780 | TTTATTATGCTTAAA[C/T]ATTTTTCATATCACT | 70348 |
rs47032518 | snp | A/G | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86321645 | GAACTTCCAAGCCTC[A/G]GCTCCCTCCAGCCCT | 70348 |
rs47035952 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Ube2cbp | Mm_Celera | 9:86440992 | TCTAATGTGACAGAG[A/C]CTTAGTAACCATCCT | 70348 |
rs47039974 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86442572 | TAAGGATGCATGCTT[A/G]GAACTTCCCTGAATG | 70348 |
rs47041550 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86363726 | GTATTGCCAAAGACA[C/T]TATGCACTTTTAGAC | 70348 |
rs47056167 | snp | A/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86329030 | TTTACAACAATGCAC[A/T]GCTTTGATCTACACC | 70348 |
rs47073182 | snp | A/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86332436 | GCCAAAAAAGATTAA[A/G]CTCATCCCCAAAGAA | 70348 |
rs47081833 | snp | C/T | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86454472 | CTCTGAACACTGATA[C/T]TCTGGGAGGTCAGAC | 70348 |
rs47108132 | snp | A/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86368185 | CTGTGGGGAGGTGCA[A/G]AGCAAGGCTTGGCAC | 70348 |
rs47126545 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Ube2cbp | Mm_Celera | 9:86446804 | AGGCCAGGATATACG[A/G]AGATCTCTTAGCTCT | 70348 |
rs47128753 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Ube2cbp | Mm_Celera | 9:86429074 | GTGCACACCGACAAT[C/T]CCGTTCCCTCTCTTC | 70348 |
rs47138995 | snp | A/T | 0.46281 | 0.131194 | intron-variant | Ube2cbp | Mm_Celera | 9:86441052 | GGCCTATGCCCTGAG[A/T]CACTGCATGCAGGTA | 70348 |
rs47141929 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86369990 | GCATCATAACCAAGT[C/T]ATTCTGCTACTTCGC | 70348 |
rs47144048 | snp | A/G | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86378039 | ACAACTAGGTAAGGG[A/G]CCACAAGGGAGTCAT | 70348 |
rs47154026 | snp | A/G | | | intron-variant | Ube2cbp | Mm_Celera | 9:86413442 | ATAAAACGCTTTTAA[A/G]AAAAAGAAATTTCCA | 70348 |
rs47164134 | snp | C/T | | | intron-variant | Ube2cbp | Mm_Celera | 9:86414678 | TAGGCATTGAGCCAT[C/T]CATCCCTCTAGCCCC | 70348 |
rs47167153 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86447661 | GAAAACCCGGCAAAG[C/G]TATGGAACACATGCT | 70348 |
rs47168661 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Ube2cbp | GRCm38.p3 | 9:86447590 | CAGGAAAGGGAGCTG[C/T]ATTCAGGAAAGGGAG | 70348 |
rs47173695 | snp | A/G | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86421587 | ATAACAACAAAAGCA[A/G]GAATGCAAATATCCA | 70348 |
rs47175326 | snp | A/G | | | intron-variant | Ube2cbp | GRCm38.p3 | 9:86319503 | TTTAAAAAACAGTTT[A/G]TATAAGCCCTTTGCA | 70348 |