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 |