| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs238379205 | in-del | -/TT | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152575 | ATACAGCTAAGATCC[-/TT]TTTTTTTTTTTTACA | 105670 |
| rs238399899 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73175912 | AGCCTCTACTTTCAC[A/G]AAGGAAATGGGGGTT | 105670 |
| rs238410041 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141190 | CCTAAAGCAACTGCT[C/T]CAATTTCAGGTCTCT | 105670 |
| rs238485678 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73157789 | AATAATATACTCCTA[C/T]GTCTAGTGTGCTTGG | 105670 |
| rs238503544 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73155042 | GACCTAGGATGTGGA[A/T]GGGGCTGATGTCACC | 105670 |
| rs238580740 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73150087 | GCCTGGAAACGGAGA[A/G]AGGAAAAGACCAAAG | 105670 |
| rs238740119 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73167555 | AAAATGTCTAAGTGC[A/G]TATTTCTATATCTGA | 105670 |
| rs238794067 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177341 | CCTCAGGCCCAGAAC[A/G]CAGACTTCCCTTGTC | 105670 |
| rs238819045 | snp | C/G | | | synonymous-codon, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73173813 | GGGCCAGTGCCGGGG[C/G]CAGTCGGTGATCCTT | 105670 |
| rs238910997 | in-del | -/CTC | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158170 | AGGACTCTGTGAGCG[-/CTC]TGGTGTACTGGGCCC | 105670 |
| rs238926212 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73166038 | GATCCATCACACCTA[A/G]CTTGTGCCAGGATGT | 105670 |
| rs238942438 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73182347 | GCTGTAGCTGTATCA[C/T]GCTAACATTCCCTCC | 105670 |
| rs238948242 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73152037 | TCTTTTTATGATTAT[A/G]GTCTGGATATTGCAG | 105670 |
| rs238958138 | in-del | -/TTTTTTT | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152574 | ATACAGCTAAGATCC[-/TTTTTTT]TTTTTTTTTTTTTTA | 105670 |
| rs239008079 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179963 | GTGGTAAGGGTAGCC[C/T]CACCCAGGTCGTTGG | 105670 |
| rs239024713 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148463 | GGAGATGTAGAGGAA[A/C]CTGTTTGCAGAGCGT | 105670 |
| rs239062186 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165446 | ATTTTCTCTTGAGTT[C/T]CTCTCTTCTCAGATA | 105670 |
| rs239067761 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159331 | AAAGGGAATTTTGAA[C/T]ACAAAGATCCACATA | 105670 |
| rs239097600 | snp | A/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73158163 | AGCCATTGAGGACTC[A/T]GTGAGCGTGGTGTAC | 105670 |
| rs239104556 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159836 | TTCCCTGCTAGTAGA[C/T]CCAGCGTTTCCAAGT | 105670 |
| rs239114353 | in-del | -/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165338 | AGGACCGCCAAGTCA[-/G]GGGTGGCACTGCTGC | 105670 |
| rs239132380 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73171202 | AAGATGGGGCTTAGC[C/T]GAAGCAGTGTCCTGC | 105670 |
| rs239165713 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165073 | AAGCAACTTGGGGAA[A/G]AAAGAGGTTTTTGGG | 105670 |
| rs239168846 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158107 | GAAACAGCTGAGGTA[A/G]TTAGTAACCAGTTAC | 105670 |
| rs239180056 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73164604 | ATGGTGGATTCCATC[A/G]ATGGCAATCCAGGCA | 105670 |
| rs239227576 | snp | C/G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73171573 | GCTCCCAGGTCTGCT[C/G/T]TCTTACCCAGCAGAG | 105670 |
| rs239235356 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147345 | AAACAATGCAGTTGA[C/T]CAACTGGGGCTGTGT | 105670 |
| rs239304989 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178091 | GTGCACTGTGTCACT[A/G]CCCACTCCCAACCCA | 105670 |
| rs239341450 | in-del | -/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73162302 | TTCCTTGAACTGCCT[-/G]GTTTGTTTTTTTTTT | 105670 |
| rs239357784 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73139388 | TTTGGTGGGTGTGAT[A/G]GATGTAGGCACTGAG | 105670 |
| rs239414611 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181248 | CATGTCCCCACCTCC[A/T]TAGCATCAGTCCTGG | 105670 |
| rs239460551 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169623 | GTCAGGCCTTGGGAC[C/T]TCCCCTTGAGCTGGA | 105670 |
| rs239512198 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73146175 | TGTCAGCTCATGTCA[C/T]TTATGGAGCAACATA | 105670 |
| rs239586518 | in-del | -/TGA | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159139 | GAGGGGCATATGGTC[-/TGA]ATGAATCATGCACTG | 105670 |
| rs239598373 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147701 | ATGCCTCCTCTTTTT[A/T]AATTTTCTTCTGAGA | 105670 |
| rs239628887 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73168838 | GTATGACACATAAAC[A/G]TCACACTACTTCCCC | 105670 |
| rs239637685 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73145474 | TTAATTTCAGCTTTA[A/T]CAAAGCTGAAGAGAA | 105670 |
| rs239639190 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144578 | CTCAGGATGGAGCAT[C/T]GAAGTATTCCCTCCT | 105670 |
| rs239703859 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73152068 | AGAATAAATGAAGCG[A/C]ACTCTAAATGTCAGC | 105670 |
| rs239740512 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73154672 | ATGAGAAGTAACATA[A/G]CTTTGTTTGTCTGGC | 105670 |
| rs239741677 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73161457 | CCATAGCCACAGTTT[A/C]ATGTGCTGCTAACAT | 105670 |
| rs239841460 | in-del | -/T | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137714 | CCTACACCCACCCCC[-/T]CTTCTCTGCCACTCT | 105670 |
| rs239855712 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73168728 | GAATTCAGTTTTATG[A/C]ACTGACGTAATTTCC | 105670 |
| rs239880052 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73149322 | AGTACATTAACTGAG[A/G]ATTGTTTTCTCAGTG | 105670 |
| rs239909545 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73171311 | TGTCCAGAGCTCTCT[C/G]CCACTTACCTGTCAC | 105670 |
| rs239918864 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73150252 | AGCACTGTCTCCTGG[C/T]CTTTTTGGGCACTAG | 105670 |
| rs239923211 | snp | C/T | | | intron-variant, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73143153 | CGGGCGAGCAGTCCC[C/T]GCTGCCGGGGAGCGG | 105670 |
| rs239942591 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73182682 | TAAATAGTAATTACC[-/A]AAAAAAAGCCATTGA | 105670 |
| rs240002411 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73149022 | GTAGAGTCACAATGG[C/T]GGTGCTCTTGTTTTA | 105670 |
| rs240036627 | snp | A/G | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73142121 | AAGCCCTGTGGAATG[A/G]AGAGATGGATTTGAG | 105670 |
| rs240109087 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178217 | CAAACCTGTTTCATT[C/T]CTAGGAAAAATTATT | 105670 |
| rs240219382 | snp | A/C | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73140851 | AAGAAACTAAAGCGT[A/C]GCCTGCCCTTTTGGG | 105670 |
| rs240266569 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73172832 | GCATAGAGTGGAGGC[C/T]CTGCTGTGCTGATTG | 105670 |
| rs240298155 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73146917 | CCCTTTCTGCTGTTC[C/T]CTCTTAGGTTCTCTC | 105670 |
| rs240355535 | in-del | -/A | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73151988 | TTAGTCAGGTTCCCG[-/A]AAGTATCCTAAACTA | 105670 |
| rs240452395 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147527 | CTGCTCTCCTGCACC[A/G]CCTGCCTTTGACTCA | 105670 |
| rs240541296 | snp | G/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141140 | AGTTTTAGCCATTTG[G/T]TCTCAAAATACTTTT | 105670 |
| rs240550906 | in-del | -/A | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177707 | CCAAGAGAACAAAAG[-/A]AGAGCCACTGATTAA | 105670 |
| rs240558557 | in-del | -/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73146364 | AGTGCACTCCTTTCC[-/G]TACGCACTGGGTGGC | 105670 |
| rs240659857 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73150672 | TGTGCCTTTTACCCC[G/T]CTGTAAGTATGCCAC | 105670 |
| rs240780729 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73162700 | CTGCAAGACGATGCA[C/T]AAAGCCCTTCTGTTC | 105670 |
| rs240789705 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144502 | AAATCCCGATACTTT[C/G]AACTCTTACCTATAC | 105670 |
| rs240815091 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73182902 | GGGGAGTCTCCCTCT[C/T]CCAGCACGTGCCAAC | 105670 |
| rs240870008 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181559 | TCTCACAGGGGAAAT[C/G]TCCTATGGGTTCGTG | 105670 |
| rs240893741 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73168283 | AGTTGCCTTGTTGCC[A/G]GGCAGTGGCTCACGC | 105670 |
| rs240933308 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181861 | AAGCCAATTCCTCAG[C/T]ACTGATTTTATATAA | 105670 |
| rs240993953 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73156648 | TACTATATACAAAAC[A/G]TTACCTCCAGAAAAT | 105670 |
| rs241054041 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73157582 | AGTAAATCTTTGTAC[A/G]TTGTGTCTCATGAGT | 105670 |
| rs241078850 | snp | A/G | | | intron-variant, utr-variant-5-prime | Rcbtb2 | Mm_Celera | 14:73143249 | CGGGGGCGAAGGCCA[A/G]GCGGAGGCCTCACCC | 105670 |
| rs241089235 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73157952 | AGGACTGCAGATTGC[A/G]TGAACCTCATTCACA | 105670 |
| rs241117281 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73174229 | AAGTTTACAATGAAT[A/G]TTCAAAGGCGTGAAT | 105670 |
| rs241146080 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179871 | AACAAAACCAAAACA[C/G]CATGCAACTGTATCC | 105670 |
| rs241148004 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73162647 | ACGGTTCTGGAGCAA[C/T]GGGGCAAGGTGGTAG | 105670 |
| rs241166225 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73167826 | CAGCGCTGGCCATTC[A/G]GCTGGGTCTGTGCTC | 105670 |
| rs241186182 | in-del | -/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73174322 | AATGCCCAGCGAGTA[-/G]GGGCCTCCTCCTTGC | 105670 |
| rs241221126 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178882 | ACCATGGACAAGCTC[A/C]ATACATGTGCTGTGA | 105670 |
| rs241296337 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179662 | TTTATTTTGAGGCAG[A/T]TCTCACTAGTCCAGG | 105670 |
| rs241299198 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160742 | GGGAGAAAGGGTTTA[G/T]TCAGTTAACACTTCC | 105670 |
| rs241369756 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179473 | TGCAGGGAGCAGACT[A/T]TATGACTGTTCTGTC | 105670 |
| rs241404193 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160340 | TTTTTAAGGCATAGG[A/G]AAACTGGAATACTGG | 105670 |
| rs241409373 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160232 | GACAAAGGTACCAAG[A/G]GTTTATTTGATTGGT | 105670 |
| rs241410375 | in-del | -/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73151170 | CTGGCTTATGTACTC[-/G]GGGGGCAGAGCAGGG | 105670 |
| rs241436042 | in-del | -/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148521 | CATATAGCCTGCTAT[-/G]GAGTATATAAATAAG | 105670 |
| rs241449271 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73154756 | CTGAGGATACAGGAA[C/T]CTGCTTAATATAGCA | 105670 |
| rs241493420 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73173085 | TGACTTTTCAGCCCT[C/T]TCCTTGTAAAGTACC | 105670 |
| rs241505641 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73166876 | CGTGTCCAGCGGGTA[C/T]GTCTCCTGGGGGGCG | 105670 |
| rs241534027 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159895 | CTCCAGGAACTTCCT[G/T]TGCTTCCCGTAGCAG | 105670 |
| rs241552570 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160854 | GAGGCCACGGAGGGG[G/T]GCCGCTTACTGGCTT | 105670 |
| rs241567640 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141261 | ATGCAGCAACTGTAT[C/T]CCTGTACTTCTTAGA | 105670 |
| rs241620333 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148971 | TAGAAGTCATCATTA[C/T]CAATATTCTATGAAA | 105670 |
| rs241788142 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73170530 | GCCTCGGTCGCAGGC[A/C]TGTGGCAAGAAAGAA | 105670 |
| rs242004210 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73145742 | GCTTCCCTTATCTGG[A/G]AGAAGCATGTGTCTC | 105670 |
| rs242011425 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73149675 | TGCCACGGGTTGTCA[A/G]TCTGTTGGTAGATTC | 105670 |
| rs242017186 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73157659 | GTCTCCAAATAGTAT[A/T]TGCATTTATAAATTA | 105670 |
| rs242209283 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73152660 | AGGAGTCCTAAGGGG[C/T]AGCGAGGGCGGCTAC | 105670 |
| rs242225010 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73182848 | AACTGGGTATGATAT[A/T]CCACATAGAAGCTGA | 105670 |
| rs242246866 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73139109 | CCGTGTGGTGAGTAT[A/G]TGAGGTGTATTCAGG | 105670 |
| rs242372239 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169381 | AGTGTTTGAGAGATT[G/T]TGAGAGTCCAGATTA | 105670 |
| rs242517717 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73176373 | GCAGGCTGCATTGTA[A/G]AGTCAGCTGCTGGGC | 105670 |
| rs242524725 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144829 | ACAATAAAATACATC[A/C]GCGTTTTAAATTTAG | 105670 |
| rs242570102 | in-del | -/A | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73168245 | GACTTGTCTTTAACC[-/A]AGATTGTTCATTCCT | 105670 |
| rs242736467 | in-del | -/AAAC | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158783 | GTTTAGTAACTGAAG[-/AAAC]AAACAGTAATTACTG | 105670 |
| rs242787401 | in-del | -/GTA | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73182321 | AAACATGGACTAATT[-/GTA]GTTAATAATTGCTGT | 105670 |
| rs242876524 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179794 | CTAACTTGTATATAT[A/T]TTTAAATTCTTAAAA | 105670 |
| rs242920040 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178247 | TCAAGCCATTCTGAT[A/G]TTAACTCCTATCCGT | 105670 |
| rs242990185 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177668 | GGGTTGAAGACCAGG[C/T]CATGCCCAGGGAAAA | 105670 |
| rs242991508 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73183952 | TAGCACTGGATTCCA[C/T]CAAGTGTCTCACAAT | 105670 |
| rs243066538 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178036 | ATTCCTTTGTGTTAT[C/T]TGGTGCTGGAACTGA | 105670 |
| rs243098531 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73154812 | GGCCTTCTGATTTTA[C/T]CATGTACTTTTTCCT | 105670 |
| rs243105452 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169082 | ATTTTATTTATTTTT[C/T]AAATTTTAATTTTAT | 105670 |
| rs243140071 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73182983 | TCTGACCAGGGATCT[A/G]TCTGGTATGAGCTTG | 105670 |
| rs243160147 | in-del | -/TTCAGCTG | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73154262 | GCTGCATTCATTCCT[-/TTCAGCTG]TCATTCATTCATTTC | 105670 |
| rs243192017 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73172132 | CACTGAGGCCCTTAT[G/T]TCTTCTGTGAGGTGG | 105670 |
| rs243210905 | snp | C/G/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73140706 | CCCACCCACAATCTC[C/G/T]GTCCTTGTTCTTAAA | 105670 |
| rs243247144 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160314 | TCCTTGTTTTAGTGT[C/T]GATAAAGGGATTTTT | 105670 |
| rs243257094 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73176133 | TGTCCCAGGCTTCTC[C/T]TTTGTCTGATTGCCT | 105670 |
| rs243257203 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73168497 | GTTCTGTGGCTGTCT[G/T]GTAAGTGCTTTCTCC | 105670 |
| rs243362933 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73175501 | CTTACATTTACATTT[A/C]TAAATGTAAATAAAT | 105670 |
| rs243372418 | snp | G/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73174122 | GAAAGCTGTCTTTCA[G/T]ATAAAAAATATATCT | 105670 |
| rs243408278 | in-del | -/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73176338 | AAGGAGGCCAGAGAT[-/C]CCCCGTCTCCCCCAG | 105670 |
| rs243410300 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147233 | TTCTGTAAATAGCCT[A/C]AGGGCCCACAGTTTG | 105670 |
| rs243418071 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73150500 | ACACTGAACACATGA[A/G]TTTTGGGGATAAATG | 105670 |
| rs243524306 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73173615 | GGGCCTATCCACCTC[G/T]GTCAGCTAGTTAGTC | 105670 |
| rs243579587 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73168784 | TTCTGGCTTCTTTGG[A/G]TAGTCACGTAACTGT | 105670 |
| rs243592399 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179239 | GGCTGTGAATTGTCA[A/C]GATAAAGAAAGGAAA | 105670 |
| rs243625670 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165789 | AGTAAAGGAATGGCC[C/T]TGGTAGTGAGGCAAG | 105670 |
| rs243626099 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179899 | TCCACATGGAGTAGG[C/T]TGGCTGGTAGTAGGG | 105670 |
| rs243665435 | in-del | -/C | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73138351 | TACCACTATGCCTGG[-/C]CAAAAAGGGACTTTT | 105670 |
| rs243672521 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73140804 | ATTTTGTTCAGAACC[C/T]TGCTGTTTCAGGCAC | 105670 |
| rs243694515 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158054 | TGGTTCAAGTGAATG[A/G]CTTGTAGACAAGTGT | 105670 |
| rs243718483 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148738 | TGGATATCCACGTCT[A/G]CTCTGGTCCTTCAGG | 105670 |
| rs243730676 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73172017 | CAAACCAAACCAAAA[C/T]AATAAAACTGATAAT | 105670 |
| rs243750378 | in-del | -/A | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163249 | ATACCCTGGGACTGC[-/A]AAGGCCAGACCCTCA | 105670 |
| rs243755882 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73154522 | GGTGACCTCTCCAGA[C/T]TTCAGGAGGATGGTC | 105670 |
| rs243790953 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73155274 | AACATTACAGTCAAC[A/C]AGCTTAAGTCAATGC | 105670 |
| rs243794317 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147484 | TTCACTTTGTCTGCA[A/G]CTTCCTTACATACTG | 105670 |
| rs243823900 | snp | C/G | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73136862 | CTGCAAATGTGATGG[C/G]CCATTAGTCCCATGG | 105670 |
| rs243863435 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160118 | TGTGGGATAGTGGTA[A/G]AAGGAACATAAAGCT | 105670 |
| rs243864752 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73153773 | ATGCTTGCAAGATGC[A/G]TTGCATTGAAGTAAT | 105670 |
| rs243902072 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147110 | TTCATTGTTTGGGAC[A/T]AAAGGTGTGTACTAA | 105670 |
| rs243964544 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177254 | TTCTGGTGATGTTGA[A/G]CCTGCGCTTTTCTCT | 105670 |
| rs243997113 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177730 | CTGATTAAAGAGAAA[A/C]GAAACATTAGCAAGT | 105670 |
| rs244036552 | snp | A/G | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73136963 | TGCCTGGCTCGGAGG[A/G]TCTCCAGTTTCAGCC | 105670 |
| rs244054025 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73145624 | ATTAAAGTCTCCGTC[C/T]AAGGCTGAAAATAAG | 105670 |
| rs244088360 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73146049 | TATTCAGGAATCATG[A/T]TGTTGAGCCAAGTCT | 105670 |
| rs244113432 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73175158 | AGTCTTGAACACAGC[C/T]CTGAACACAGCCTTG | 105670 |
| rs244122662 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73151988 | ATTAGTCAGGTTCCC[A/G]AAGTATCCTAAACTA | 105670 |
| rs244160929 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152344 | AGTAATTTGTCTTGA[A/G]TTATTTTTAAACTTT | 105670 |
| rs244231538 | snp | A/G/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73161343 | GGGCGGGGGGGGGGG[A/G/T]GGGGACCATGCTAGA | 105670 |
| rs244247612 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73180884 | GGGTAAGAGGAAGTA[C/T]TGGATGACGTATGAG | 105670 |
| rs244282914 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144407 | GGCATGCAGGTAAGT[C/T]AGTTTCCAGGGCTAC | 105670 |
| rs244430088 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73161387 | ATGCTCTTTAAGACC[C/T]TCCTTCCCCAGCCTC | 105670 |
| rs244477321 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73156763 | TAGACTGTAGTTTAA[A/C]CTGAATTGTGACAGC | 105670 |
| rs244525109 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73155884 | AGATATTGTTTTGCA[C/T]CCTATATCCAGTGGA | 105670 |
| rs244621658 | in-del | -/ACTTACACTGTACAAAGATGTAGCAGCT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73161383 | GATATGCTCTTTAAG[-/ACTTACACTGTACAAAGATGTAGCAGCT]ACCCTCCTTCCCCAG | 105670 |
| rs244672795 | snp | A/T | | | downstream-variant-500B | Rcbtb2 | Mm_Celera | 14:73184077 | TCTTAAATTGTTGAG[A/T]AACAAAATCAAAGTA | 105670 |
| rs244711642 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73156253 | AGATTGAGAAACTTA[A/C]AAAATGTAGTAGAGG | 105670 |
| rs244775250 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73151762 | TACAAGGTTCTCGCT[C/T]GAAGACACTTTAAGT | 105670 |
| rs244776992 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73175939 | GGTTTAGTTTACTGT[A/G]ACAGAGCAAACACTG | 105670 |
| rs244808989 | in-del | -/A | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179144 | GATGATTCTGTCCTT[-/A]AAGAGCACATACTCG | 105670 |
| rs244810297 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73145282 | GTAAAGGACTTAGAG[A/G]GGACATGGATGAAGA | 105670 |
| rs244910874 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73153991 | GCGCCACCATGCCCG[A/G]CTCTAGATACAGTTT | 105670 |
| rs244958335 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147391 | ACTTACATTACCTGT[A/T]ACTCGGGGATGACAC | 105670 |
| rs245038361 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73183397 | TTTTAGCCTCTAACA[C/T]AGTACCTTATATATA | 105670 |
| rs245067542 | snp | C/T | | | downstream-variant-500B | Rcbtb2 | Mm_Celera | 14:73184184 | TATAGCAAAGTTGAC[C/T]CTAAGATATAAATGG | 105670 |
| rs245093153 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152325 | GTTTACATTATTTCA[C/T]ATTAGTAATTTGTCT | 105670 |
| rs245224281 | snp | A/C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73171089 | GAGTTCACTGCAGCA[A/C/T]GGCTTCAGCCATGCA | 105670 |
| rs245254559 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181958 | CAGAGCTTCACCTGT[A/G]CTAAGCACACAGTCT | 105670 |
| rs245267091 | in-del | -/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73157693 | TATCAGTCTGCTATG[-/T]AATAGTTCCCTCATG | 105670 |
| rs245276908 | snp | A/C | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73177968 | GATGCTGAAGCGAAG[A/C]GGGGCAGAAAGATGG | 105670 |
| rs245311830 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73156659 | AAACGTTACCTCCAG[A/G]AAATCTACAAAAGGT | 105670 |
| rs245357106 | in-del | -/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73153150 | AGCTCTAGTAACAAA[-/G]GGTTGTGGTCTCCTC | 105670 |
| rs245359600 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73170412 | CGCTTGCTGGTGTCC[A/G]CACAAGTGTACTTGG | 105670 |
| rs245397529 | in-del | -/TGTTTCAGTTTT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73161179 | AGGATGAAATAGATA[-/TGTTTCAGTTTT]TGTTTAATATGTTTG | 105670 |
| rs245402843 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73170776 | TGCTCAACCAAACGA[A/G]ACGCTTTTAAAAGGT | 105670 |
| rs245439789 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163526 | TTTCAGTGTTAGTAA[A/G]CCACATGTGATCTAA | 105670 |
| rs245441336 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169812 | TCATCAACGCTCCCT[C/T]CCTCTGAGTCCTGGG | 105670 |
| rs245534620 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73180115 | ATGAACAGTCTTACT[A/G]TGTGATGGAGCGTGG | 105670 |
| rs245546831 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169203 | CCACCCCGTCTCCAC[A/G]TAGATGCCCCCACCT | 105670 |
| rs245567437 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73168381 | GAGTGAGTTCCAGGA[C/G]AGCCAGGGCCACACA | 105670 |
| rs245569732 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73161900 | TTGTTTGTGTGTTTG[A/G]TTGGTTGTCTCAGTA | 105670 |
| rs245603567 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144906 | CAATGTGTCAGGGTA[G/T]CCCAGGTTGGCCTGG | 105670 |
| rs245603628 | snp | A/G | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137334 | CATCTCTATTTGTAA[A/G]TAGGGATGTAATTTC | 105670 |
| rs245621664 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73182032 | ATGAAGTCCACCCAT[C/G]CCACCCATTGTCCTG | 105670 |
| rs245628664 | snp | G/T | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137980 | TTGCATTTGTGTGTG[G/T]GGGACCGAGTATGCA | 105670 |
| rs245640130 | in-del | -/ATTTT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73139623 | TTATTCTATTTTAAC[-/ATTTT]ATTTTTTTTACTTTT | 105670 |
| rs245648827 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73161082 | GCAACCAGTCCAGCC[C/T]AGCCCACAAAGGGCA | 105670 |
| rs245657270 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73162734 | GAGTGGAATCATTGC[A/G]TGACAACGCTACTTA | 105670 |
| rs245738128 | in-del | -/A | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73156797 | CAGTTTGCTGTGCTC[-/A]TACAGTGGATTTCTC | 105670 |
| rs245767142 | in-del | -/AT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73167666 | TTTTCCACATTAAAC[-/AT]GTTTTCCTTCAAGAA | 105670 |
| rs245793533 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73173705 | ATGTGCCTCTGTGGC[A/G]TTTGCTTGTGAATTT | 105670 |
| rs245794992 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160627 | TGAACCTGCTTATCA[C/T]CATAATGGGCATCAC | 105670 |
| rs245871183 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73152798 | TGCTGGCATTGAACC[C/T]GGAACCTCACTCATC | 105670 |
| rs245883587 | snp | A/G | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73142373 | TAATACAGAGCCCCT[A/G]TTTCAAAGCCATAAC | 105670 |
| rs245907330 | snp | A/C | | | intron-variant, utr-variant-5-prime | Rcbtb2 | Mm_Celera | 14:73143431 | GGTGCGCATGCGCGC[A/C]GGCCCAGCCCGGGGT | 105670 |
| rs245908069 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73166349 | GTGTTCTGTAATACG[C/T]TCTCTGCCTGTACTG | 105670 |
| rs245955521 | snp | A/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141516 | AGCCACTTACTTTGA[A/T]CAAAAGGACTGTTGA | 105670 |
| rs245990682 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148951 | TGGCAGAGGGAATCT[G/T]GGTTTAGAAGTCATC | 105670 |
| rs246012339 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159917 | CCGTAGCAGATTGGG[A/G]CTACTGAGTCCACAC | 105670 |
| rs246041125 | in-del | -/ATA | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73161917 | TGGTTGTCTCAGTAT[-/ATA]CTAAGTCTGATTCCT | 105670 |
| rs246059992 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141064 | TGAAACGGGGTTATC[C/T]ATGATGGTGCATGCC | 105670 |
| rs246117037 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73174056 | AACTAAAACTATTGG[A/G]AACTAACACAATACT | 105670 |
| rs246182021 | in-del | -/CAGG | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141216 | CTCTTGGTCCATCGT[-/CAGG]CATCATATGCCATCC | 105670 |
| rs246245776 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73139755 | CTCGAGTGTGTTATA[C/T]GAATGGTGGTGTCTT | 105670 |
| rs246285713 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73140386 | CTGATGACATCCACA[A/T]ACGCCTTTGATTTTA | 105670 |
| rs246320209 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73145728 | AGGTGACTCTTCTCG[A/C]TTCCCTTATCTGGAA | 105670 |
| rs246322600 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73155708 | CCAGTATCCAGTGAT[A/G]CTGTTTCCCACCCAG | 105670 |
| rs246341518 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73140312 | TGCCTTGCCCCTGGG[G/T]AGTTTTAGTTCTCCT | 105670 |
| rs246387961 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148711 | CTGTTACTCTGAAGA[A/G]TTGTCCCAATATGGA | 105670 |
| rs246482951 | in-del | -/GGAT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178344 | CTCATTTTGCCCGAC[-/GGAT]GGAAGCCCTTCACAG | 105670 |
| rs246498615 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158331 | AAGGCCACTAATAAC[A/C]TCTCCATTAGATTCT | 105670 |
| rs246514214 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73155968 | AGATATTGTTTCACA[A/T]ATTTCAGCCTGCCTA | 105670 |
| rs246667214 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73176077 | TGTGGCAATCTTCCT[C/T]TTTCTGAGGCATGAC | 105670 |
| rs246824145 | in-del | -/TTTTTT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73139628 | TATTTTAACATTTTA[-/TTTTTT]TTTTTTTTACTTTTT | 105670 |
| rs246865358 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181436 | TTCCGTTTTGTCTTC[A/C]AGAGCTCATGTGGGG | 105670 |
| rs246876037 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181076 | ATTTATTTAATCCCA[C/T]GAACTCTTTCTGAAT | 105670 |
| rs246892258 | snp | A/G | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137568 | CTAGTCAGGCTCTGA[A/G]AGAACAAGAGGCGAA | 105670 |
| rs246894625 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178832 | AGAACTGTCTCCAAA[A/T]TGTCCCCGAGCTCCA | 105670 |
| rs247077315 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73157520 | TGTAGGCATTTCTGG[A/C]ACACAGAATGGTTGA | 105670 |
| rs247095916 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163996 | CAGAGGAAAAAAGAT[C/T]TACATCATAGAAGAT | 105670 |
| rs247205016 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73162611 | GTGAGCTTGGCCACG[C/T]GTTGGGCAACATGAA | 105670 |
| rs247242780 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179111 | GAATGGCAAACATAA[C/T]GAATGAGAGAAGCAG | 105670 |
| rs247246783 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178347 | ATTTTGCCCGACGGA[C/T]GGAAGCCCTTCACAG | 105670 |
| rs247309046 | snp | A/C | | | downstream-variant-500B | Rcbtb2 | Mm_Celera | 14:73184500 | AGGCTAAGGCAGACT[A/C]CTGAAGGAATGTTTA | 105670 |
| rs247328168 | in-del | -/A | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73172222 | GAAAAGCATATACTT[-/A]AGAAAACCAGATCGT | 105670 |
| rs247347120 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178152 | TGTGTGCTGGTGGGC[A/G]TGGCCTCCAAAGATT | 105670 |
| rs247357705 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73170042 | CAACGCCTTAGACCG[A/C]CAGCCAGCCAGCCAG | 105670 |
| rs247406414 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73153529 | AAGCAGGCCTTTAAC[A/C]CTGACTTTTCAAACT | 105670 |
| rs247421473 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73183563 | AGTAGCTAATTTAGA[G/T]CATATTAGCATTCAT | 105670 |
| rs247465252 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165660 | CTATAGTTGTACAAC[A/C]AAGACTGTTTACCAA | 105670 |
| rs247467244 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159630 | TTTAAAGGGAGCCTT[A/T]CCTGAGGAAGTGTCC | 105670 |
| rs247485171 | snp | A/C/G/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73159173 | GGATTTTTGTGATCC[A/C/G/T]CCAAGACTATGATCC | 105670 |
| rs247522241 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73153018 | TGTTCGAGACCCGAG[C/G]TCTGATCCCTAGCAC | 105670 |
| rs247549734 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73145256 | CAGACAAATGTAAGC[A/G]GCCATTGGCTGTAAA | 105670 |
| rs247555943 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160064 | ATTCAAGCAGAAAGC[A/T]GAAGTCTAGGGAGCG | 105670 |
| rs247573187 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73176088 | TCCTCTTTCTGAGGC[A/G]TGACACGTAGCATTC | 105670 |
| rs247601339 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158754 | CACTGATACTGTTTG[A/G]CAAAATGCTCTGGTG | 105670 |
| rs247624862 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144330 | TGGTCACTGTTTAAC[C/G]GTCATTGAGTCCGCT | 105670 |
| rs247665870 | in-del | -/TT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73174732 | CAGATATCCTGACTC[-/TT]GAGTAAGGGAACTGT | 105670 |
| rs247697162 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181764 | ACTTTGAATATGAAC[A/G]GGTGGTGGTACCTTT | 105670 |
| rs247727568 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73176407 | CCACAGCAGCAGCAG[C/T]AGGCTGCAATGTAGA | 105670 |
| rs247732691 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73182189 | CAAGCATTGAAAGGG[A/G]AGGAAGGAATGACTG | 105670 |
| rs247787168 | snp | C/T | | | utr-variant-5-prime | Rcbtb2 | Mm_Celera | 14:73138800 | AGACACTGTCAAGAA[C/T]GTCCCGGTGTGATCA | 105670 |
| rs247842383 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73149031 | CAATGGCGGTGCTCT[G/T]GTTTTAGTGTTGGTT | 105670 |
| rs247852425 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163363 | AACCATCCCTGAATT[C/T]GCAGCTATAGATCTG | 105670 |
| rs247857696 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179732 | CTTGCCATTTTCTTG[C/T]CCTTGGGCTCTTAAG | 105670 |
| rs247884100 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158091 | AGCATGCTTGAAAGG[A/T]GAAACAGCTGAGGTA | 105670 |
| rs247941609 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148496 | TATGGACTATGTAAA[C/T]AAGCCAAGTCATATA | 105670 |
| rs247963176 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73162781 | GCCTACACTTTGAAC[C/T]TAGATTCCTGGGCTG | 105670 |
| rs247967715 | in-del | -/TTTTT | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73154298 | TTCATTCATTTCTCC[-/TTTTT]TTTTTTTTCCAGCTT | 105670 |
| rs248015751 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73154793 | GTGTGCCTTCATGTG[G/T]CCTGGCCTTCTGATT | 105670 |
| rs248037152 | in-del | -/GGATGGATGGATGGATGGAT | | | downstream-variant-500B | Rcbtb2 | Mm_Celera | 14:73184345 | TAGATATGGAAGGAA[-/GGATGGATGGATGGATGGAT]GGATGGATGGATGGA | 105670 |
| rs248044278 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73156426 | TATGTCTGTCTGTCT[C/T]CTCTCCCCCTCTCCC | 105670 |
| rs248110341 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73155585 | GATGCTGTTTCCCAC[C/G]CAGTATCCAGTGATG | 105670 |
| rs248125867 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147785 | TCTTCAGGCTGTCTG[A/C]AGCACTTGAGAGGTG | 105670 |
| rs248156204 | snp | C/G | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141299 | TTGTTTGTTCGTTTT[C/G]TTTGTTTCTTCGTTT | 105670 |
| rs248181836 | in-del | -/GTGTAATG | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73167319 | AAAAATAATTTACTA[-/GTGTAATG]GCAAATGAACAATTA | 105670 |
| rs248209063 | snp | A/G | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137086 | TTGTTTTTGTTTTTT[A/G]TTTTGTTTTGTTTTT | 105670 |
| rs248241960 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | Rcbtb2 | Mm_Celera | 14:73142508 | GATCACTAGCCCCAC[A/G]GGCTCCCTTCTCCCT | 105670 |
| rs248403037 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152178 | CCCCCCCCCCACACA[C/T]ACACACACACACACT | 105670 |
| rs248421055 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165350 | TCAGGGGTGGCACTG[C/G]TGCCAGAGAATGGGC | 105670 |
| rs248470123 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73174890 | CTGGGTTTGTTCAGG[G/T]AATAAGCCATGGAAG | 105670 |
| rs248573307 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73168200 | CTTGGAATTCATAGT[A/G]TAGAATTGTGGGAAA | 105670 |
| rs248676841 | in-del | -/G | | | intron-variant, utr-variant-5-prime | Rcbtb2 | Mm_Celera | 14:73143320 | AGCGCCAACCCACCC[-/G]GGGCCGGGGCCCGGC | 105670 |
| rs248788228 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73146594 | GGCCTAGACTGTTTT[C/T]AGCCTTTGAAACTGA | 105670 |
| rs249004420 | in-del | -/TGGGGGCGGGGGGGGGGG | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73161325 | AAGACTAGGTCTCCC[-/TGGGGGCGGGGGGGGGGG]GGGGGCGGGGGGGGG | 105670 |
| rs249011404 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73167008 | CTTCAGGGAGATGCT[A/G]TGTCTATGGTCCTGG | 105670 |
| rs249063906 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73149161 | GTGCTAGCACAGCGA[G/T]CCGATCCTGCTGATT | 105670 |
| rs249083795 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73161150 | GGGACTGGGAAGTCA[A/C]TAACTGTGTTTCCTA | 105670 |
| rs249157782 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73155016 | GACATGCCAATACAT[A/T]ATAGTATAGGGACCT | 105670 |
| rs249205898 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177158 | CAGAGACCTTACCAC[C/G]AAGTTGGCAAATGTT | 105670 |
| rs249245544 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73180062 | GGAAGGCTAGATTAA[C/G]GTTCATGTCAAGAAT | 105670 |
| rs249254897 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148154 | GCCTACAAAATATAA[C/T]ATATTCAAATGAGGA | 105670 |
| rs249276778 | in-del | -/A | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141559 | TTTAAATGGCTAACC[-/A]AAACATGCCTACTTC | 105670 |
| rs249281031 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73173928 | GGTAAGCTTGTCCTT[G/T]CCCTCTTGGGACAGT | 105670 |
| rs249293739 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141726 | CTTTGTCAGGTTTTA[C/T]CAACATGCTTTGTGA | 105670 |
| rs249372098 | in-del | -/GGGATG | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73180034 | TGATGTCTTAGATGT[-/GGGATG]GGGATGGGGAAGGCT | 105670 |
| rs249390814 | in-del | -/A | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73157570 | CATGTGATGTGCAGT[-/A]AATCTTTGTACGTTG | 105670 |
| rs249525966 | in-del | -/TC | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179644 | GATCCCCAGCTGTCT[-/TC]TGTTTATTTTGAGGC | 105670 |
| rs249558856 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73183314 | TGATAGTTTGCTAAT[C/T]TGGAGAAATGGTTCA | 105670 |
| rs249570833 | in-del | -/CCTT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73167055 | ATGTAGGCTTCACAC[-/CCTT]CCTTTCCTGTAGCGT | 105670 |
| rs249578715 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73139628 | CTATTTTAACATTTT[A/G]TTTTTTTTACTTTTT | 105670 |
| rs249609362 | in-del | -/TGTCATTCT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158858 | TATGAAAGTAGAAGG[-/TGTCATTCT]TGGCATAGGGCTTGC | 105670 |
| rs249665262 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73170749 | AATAAAACCTATGTA[C/T]ACTGGATTCTCTGCT | 105670 |
| rs249684711 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73172159 | GTGGGAGCAGTGGGC[A/G]CATTTTCCTTCTAGT | 105670 |
| rs249721358 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73172834 | ATAGAGTGGAGGCCC[G/T]GCTGTGCTGATTGCT | 105670 |
| rs249742414 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73146472 | TAGCAGCTGACTGTT[A/G]ACATTATTTTTATTC | 105670 |
| rs249791208 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73171463 | CCTCTTTCCTGTCTT[A/G]CTATGCCTCTCTGCC | 105670 |
| rs249855604 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163754 | CTCCTGCTCTTCCCT[A/G]TCTTGGTCTCTCTGG | 105670 |
| rs249861832 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73145852 | CTCGAGTGTGTGTTT[C/T]TAATGTCTTCAGCTC | 105670 |
| rs249863379 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73156630 | ACAGCAGTGAAATTA[C/T]CTTACTATATACAAA | 105670 |
| rs249900783 | in-del | -/AAGC | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73150556 | GTCCATATATGCATT[-/AAGC]AAATAAATAAATAAA | 105670 |
| rs249925477 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169664 | GGCCTGTCGTTGGAC[C/T]TTTTTCCTCAGTCTC | 105670 |
| rs249944723 | in-del | -/GT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73145319 | ATTTTAGGACATGAA[-/GT]GTGTGGTTCCCTTGA | 105670 |
| rs249959288 | in-del | -/CACA | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178950 | TGCACCATGGACAAG[-/CACA]CACACACACACACAT | 105670 |
| rs249979880 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73153912 | ACTCACTCTGTAGAC[C/G]AGGCTGGCCTCAAAC | 105670 |
| rs250024186 | snp | C/T | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137879 | CATGCAATGCTGGCT[C/T]GGTGGCCTTTGTCAC | 105670 |
| rs250095767 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169468 | CAGTTTTTCCTAATT[C/T]AACAACAGGGGTCAG | 105670 |
| rs250116339 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73176663 | CTTGGGGTTGATTTG[C/G]AGGTTTTGTTTGGGG | 105670 |
| rs250136123 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169920 | CCTTTGACTCCTTAA[A/G]TGGGGAACAGGAGAG | 105670 |
| rs250150726 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73143865 | TGTAGCAGAGGACAC[A/C]GAGGTGCTGCTCCCT | 105670 |
| rs250164541 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73175982 | CTACACCATGACAAC[A/G]CACTTTATCATATGA | 105670 |
| rs250198239 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181659 | TTTAGAGGAAAGACT[A/G]TAATAGGCAATGGAC | 105670 |
| rs250200721 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73176482 | GCAGGCTGCATTTGC[A/G]GTCTTGCCGATTAGG | 105670 |
| rs250242890 | in-del | -/TGTA | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179811 | TAAATTCTTAAAACT[-/TGTA]TGTATTTTTAAATAC | 105670 |
| rs250253015 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73149928 | TTCATAAGATGATGT[A/G]TTAGTCAACATTGTG | 105670 |
| rs250253375 | snp | G/T | | | intron-variant, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73142932 | TCGCCGATCCCGGCC[G/T]AGGAGGGAGGCGGGG | 105670 |
| rs250259186 | snp | G/T | | | intron-variant, utr-variant-5-prime | Rcbtb2 | Mm_Celera | 14:73143618 | GCCGACCCCATGGCG[G/T]CACACGCTTTAGGCC | 105670 |
| rs250306216 | snp | A/C | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73145098 | GAACATTGACAGAGT[A/C]TAGACTTGCTGGGGT | 105670 |
| rs250344700 | in-del | -/GT | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73166894 | TCCTGGGGGGCGGGG[-/GT]GGCGGTGCACCAGAG | 105670 |
| rs250371985 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73151150 | TTTATTGTGTGCCTG[A/G]ATGTCCTGGCTTATG | 105670 |
| rs250387026 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73150727 | AGTCTCTGAGGGTCT[A/G]GGGGATACAGATGAA | 105670 |
| rs250411079 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73149122 | TGAACTCCTGACCTT[C/T]CTAAGGACAGGGATC | 105670 |
| rs250412824 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160529 | GAGATGCTGCTGCAC[A/T]GTTGGATGTATTAAA | 105670 |
| rs250418042 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144708 | CGTAGCCAACTTTCC[A/G]TATCCTTATATTCTG | 105670 |
| rs250568100 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73150208 | ACATGGCTGCCCAAA[C/G]CATCTCTAACTCCAG | 105670 |
| rs250709721 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73140985 | ATGCTACCCTAGCTC[C/T]GTGACAACTCTGCCT | 105670 |
| rs250785364 | snp | C/G | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141932 | CCTAAGCTGAACTTT[C/G]AGCCTCAGGAACCGT | 105670 |
| rs250866479 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159570 | GGATGGTTGGTTCTT[A/G]GTGACGGTTGCTTTG | 105670 |
| rs250887101 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73153431 | GAAAAACTTTAAGTG[A/G]TCTCTCTTTGGTTTT | 105670 |
| rs250907678 | in-del | -/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73146872 | AGAGCTGCCTCCTCT[-/C]TCTCTCTCCCTCCCC | 105670 |
| rs250963891 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147352 | GCAGTTGACCAACTG[A/G]GGCTGTGTTTTGTCA | 105670 |
| rs251005413 | in-del | -/TTACTCATTCCATGTCC | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137752 | CTCTGGGAACTGTCT[-/TTACTCATTCCATGTCC]TTCTGGTGTTTACAA | 105670 |
| rs251061422 | in-del | -/TTTTG | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73183136 | GTGTGTGTGTGTGCT[-/TTTTG]TTTTGTTTTGTTGTC | 105670 |
| rs251104296 | in-del | -/AG | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73172781 | CAATTATAGACGTGA[-/AG]AGAGAGAGAGCAGGA | 105670 |
| rs251128232 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147435 | TGATACTGTTTGATT[A/T]CTCTGTGAACACGTG | 105670 |
| rs251139500 | in-del | -/ACAGATG | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73164158 | AATGTGGTAGAAAAC[-/ACAGATG]ACAGGGAGCACACAT | 105670 |
| rs251211252 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181822 | AGAACACTCCCTTAG[A/G]AAGCCTACTCTGCCC | 105670 |
| rs251476325 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73162634 | AACATGAAGCAGGAC[G/T]GTTCTGGAGCAATGG | 105670 |
| rs251504044 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73162995 | ATGCCAGGATAGGCC[C/T]GATTATTCAGACCAT | 105670 |
| rs251569223 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73168174 | CAGTCGTCTCTAGTA[A/G]TTAAACAGCTCTTGG | 105670 |
| rs251593105 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73170990 | AGAATGCTAGTGAGA[A/G]TTGAGATGTCTGAGT | 105670 |
| rs251609587 | in-del | -/TAA | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73157857 | AGGAAGGAATGGTGG[-/TAA]TGTCTTATTTTATGT | 105670 |
| rs251669981 | in-del | -/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73168918 | TTATCCCACATGGTA[-/T]TTTTTTTATTTGATT | 105670 |
| rs251685283 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179947 | CTGTGTCCACCAGTA[A/G]GTGGTAAGGGTAGCC | 105670 |
| rs251746830 | in-del | -/ATCT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165513 | GAACTTATAAAATGA[-/ATCT]ATCTATCTATCCATC | 105670 |
| rs251750716 | in-del | -/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181091 | TGAACTCTTTCTGAA[-/T]TCCATTTTAAAAATA | 105670 |
| rs251805044 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159857 | GTTTCCAAGTATCTG[C/T]TGTGGACTAGGGACC | 105670 |
| rs251848166 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73155341 | TGATGCTGTTTCCCA[C/T]GCAGTATCCAGTGAT | 105670 |
| rs251852830 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73145947 | AGTGCTGATGAATGA[A/T]AGCTAAACTTGAGTG | 105670 |
| rs251882796 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160209 | ACCTTGCACCGTTCC[A/G]GGAAAAAGACAAAGG | 105670 |
| rs251908983 | in-del | -/A | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73157714 | TTCCCTCATGGATTT[-/A]AAAGATGGATTTTAT | 105670 |
| rs251938180 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165225 | ACGGAGGAACTCTAC[G/T]TCCTGGCTCGCTTCC | 105670 |
| rs251950848 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178108 | CCACTCCCAACCCAA[C/T]CGGCTTTCTTTTTAA | 105670 |
| rs251981460 | snp | A/C | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73140673 | GCCTGTTGAAATCTG[A/C]TCTGCTCGTCCTAGC | 105670 |
| rs251986163 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73171147 | TCTCATTGCAGGGCC[A/G]AGTCTGACTCCTCCT | 105670 |
| rs251992938 | in-del | -/A | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181323 | CGGTGCCACTCTGTC[-/A]TGTATACTTTCTTAT | 105670 |
| rs252089509 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73140133 | GACCGTGAGACTGTT[A/G]AGGCAAAGGGCAGAC | 105670 |
| rs252147785 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73167088 | TGGACAACATATACA[C/T]CAACAGTTTTAAAAA | 105670 |
| rs252180447 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73161685 | CAGCAACACACAGCA[C/T]CAGATGTGGGTGACT | 105670 |
| rs252225188 | snp | C/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73159059 | AAGTTAAGTATATAA[C/G]TAAAAGTGTCTCCAG | 105670 |
| rs252225492 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73172973 | GGAGGCCTGGAATCC[A/C]TTCAGTAGATTCTGT | 105670 |
| rs252290313 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141224 | TCCATCGTCATCATA[C/T]GCCATCCAGGGTACC | 105670 |
| rs252325872 | snp | A/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141841 | TTTCTGGCCTTCCAC[A/T]TCTAGTCCTAACTTC | 105670 |
| rs252396302 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147688 | ATTTCTCTGAGGAAT[C/G]CCTCCTCTTTTTAAA | 105670 |
| rs252447973 | snp | G/T | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73136795 | CTTTGAGATGTACCT[G/T]CGATCATCAGTCCAG | 105670 |
| rs252499843 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163957 | TTAGAATATCAGACA[A/T]GATGGCAGAAAAGAA | 105670 |
| rs252536617 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158918 | GCTGGAAATAAGGGC[A/G]TGCAGCCACCCATCA | 105670 |
| rs252536675 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73164285 | CTGAGTAGTATGTGG[G/T]TGTTATGATTTCTTA | 105670 |
| rs252612714 | snp | A/G | | | missense, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73177035 | GAAGACAGTGAAGAC[A/G]ATATTGTAGAAATGA | 105670 |
| rs252656590 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181264 | TAGCATCAGTCCTGG[C/T]GTGGGTGGGCATCCC | 105670 |
| rs252682286 | in-del | -/TTT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165098 | TTGGGTTTTTTTTTG[-/TTT]TTTTTTGTTTTTTGT | 105670 |
| rs252701711 | snp | A/G | | | utr-variant-5-prime | Rcbtb2 | Mm_Celera | 14:73138874 | ATGTGAGTAGAAATC[A/G]GGGATCTCTGAAGGA | 105670 |
| rs252728396 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169636 | ACCTCCCCTTGAGCT[A/G]GATTGCACTTTGGGC | 105670 |
| rs252776774 | snp | A/G | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73142205 | CCTAAACTGATGTGT[A/G]TGTATATATATATAT | 105670 |
| rs252787224 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73145170 | CCTTAATGTCCCCCG[A/C]CATGAAGTCATGGAG | 105670 |
| rs252893874 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179511 | CTGGCTGCCCCCAGC[A/T]CCCCAGGGCAGAGCT | 105670 |
| rs252969381 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144658 | TATAGGAAAAACTAA[C/G]CAAATAACCTCTGCA | 105670 |
| rs252994324 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73172650 | TCAGCTGGTCACTCA[C/T]TTCCCTGCGGTTTCG | 105670 |
| rs253003290 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73158898 | GAGGAAACATGGAGC[A/G]GAGAGCTGGAAATAA | 105670 |
| rs253030521 | in-del | -/CAGACAGAAA | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169707 | TCCCTGTAATTCCTT[-/CAGACAGAAA]CAATTATGGGTCAGA | 105670 |
| rs253080489 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177809 | GGTGAGTATTGAATA[A/C]GAGGACTCCAGATCA | 105670 |
| rs253082641 | in-del | -/ACCGTAC | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73156840 | GCCTGTTTGTTCCAG[-/ACCGTAC]ACCCAGACTAACAGG | 105670 |
| rs253107481 | snp | G/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73153158 | TAACAAAGGGTTGTG[G/T]TCTCCTCTCTTGAAC | 105670 |
| rs253117566 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160483 | AAGAGCTTTGTTGTT[A/G]CCCTTGTCCTTGTGC | 105670 |
| rs253135507 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73182801 | TCTATCTGCCTACCC[C/T]GAGATTTACAGTAGC | 105670 |
| rs253171210 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177429 | ACTGGAGCATCACAG[A/G]CAAGCATGGAAGGAA | 105670 |
| rs253212237 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147511 | ACTGATACTGTAAAC[C/G]CTGCTCTCCTGCACC | 105670 |
| rs253221758 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73152664 | GTCCTAAGGGGCAGC[A/G]AGGGCGGCTACCTCT | 105670 |
| rs253238217 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181866 | AATTCCTCAGCACTG[A/G]TTTTATATAAATACA | 105670 |
| rs253312833 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141293 | ATACTCTTGTTTGTT[C/T]GTTTTGTTTGTTTCT | 105670 |
| rs253541251 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163100 | AAGGATAGGGTCAAG[C/T]AAGGGTAGAGGAGAC | 105670 |
| rs253620151 | in-del | -/ACACAT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165581 | ATCTTATCATCGCAC[-/ACACAT]ACACACACACACACA | 105670 |
| rs253633734 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73145576 | GTTGGGGAAAGGATG[C/T]TGGGAAAAGAATCAT | 105670 |
| rs253739336 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178910 | TGACATGCACCATGG[A/C]CAAGCTCCATACATG | 105670 |
| rs253749265 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73183764 | ATTGAGGGTCTCTCT[A/C]TATAAGATTGATTAT | 105670 |
| rs253811299 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73150681 | TACCCCTCTGTAAGT[A/G]TGCCACTGTCCCTAG | 105670 |
| rs253822305 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147818 | TCTTTCTGTCTTCAC[A/G]GTTATGTTCTTTTAC | 105670 |
| rs253836103 | in-del | -/AA | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165604 | CACACACACACACAC[-/AA]ACACACACACACACA | 105670 |
| rs253863918 | snp | C/T | | | utr-variant-5-prime | Rcbtb2 | Mm_Celera | 14:73138860 | TCAGCTGAATTACCA[C/T]GTGAGTAGAAATCGG | 105670 |
| rs253886280 | snp | C/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73154272 | ATTCCTTCAGCTGTT[C/G]ATTCATTCATTTCAT | 105670 |
| rs253996276 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73153724 | TTGACTTTTAGTGAC[G/T]GAAGCAAACACCAGA | 105670 |
| rs254111322 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73180674 | AGGGACAGTTGCTAG[A/T]GCAGGTCCTCAAATA | 105670 |
| rs254114479 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73174304 | GGGATTCAGCATTTC[C/T]GGAATGCCCAGCGAG | 105670 |
| rs254144743 | in-del | -/A | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73153193 | TGCCAGTTGATAGAG[-/A]AAATAAGTCACATAG | 105670 |
| rs254146741 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181285 | TGGGCATCCCTCCAA[C/T]ATTCTGTAGAACTCA | 105670 |
| rs254148463 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158115 | TGAGGTAGTTAGTAA[C/T]CAGTTACTGCAGCTT | 105670 |
| rs254184007 | in-del | -/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178406 | GGCGCTCAGAGCGCA[-/C]CCACAATACATTCTC | 105670 |
| rs254266849 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148989 | ATATTCTATGAAATT[C/T]CTGTGTTCATGGTAA | 105670 |
| rs254275104 | in-del | -/ATCC | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73173497 | ACTGGTAATCAATAG[-/ATCC]ATCCTCATGTTATAA | 105670 |
| rs254337292 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73171896 | GGAGGCAGAGGCGGA[A/G]GCGGAGGCAGAGACA | 105670 |
| rs254359797 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163462 | CATGCAGATCCTTTG[G/T]AGCATGAGTTGCCTC | 105670 |
| rs254365987 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73150509 | ACATGAGTTTTGGGG[A/C]TAAATGTGTGAAATT | 105670 |
| rs254430922 | in-del | -/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73162320 | TTGTTTTTTTTTTTT[-/C]CCACAGATTTTTGTG | 105670 |
| rs254433789 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165684 | TTACCAATGAAAGGT[C/T]CAAGAATCCAGTAGT | 105670 |
| rs254530404 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181228 | CTCTAAGACACTGAA[A/G]TGCTCATGTCCCCAC | 105670 |
| rs254558926 | snp | A/G | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137238 | ACTGGGGGCCTTGAG[A/G]GTAGGACAGGAAAGA | 105670 |
| rs254608568 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73140491 | TGCCCAGAGATCTGG[A/G]GTCCCAATCCTGCTG | 105670 |
| rs254717617 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147043 | TTCTTTTTTTTTTTT[A/T]TTTAGAAGTCATTTT | 105670 |
| rs254733429 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144383 | AAATCTGTCACCGTA[C/T]TGGACAATGGCATGC | 105670 |
| rs254803932 | snp | A/G | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141908 | ATAAGTTCACAGACT[A/G]TTGTTTAGCCTAAGC | 105670 |
| rs254857973 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73164231 | TTTTGTGGAAGGTGC[A/G]CATATCGAGGGCTTT | 105670 |
| rs254888456 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159279 | GATGAGGTCATAAAG[G/T]TTGGTACTAATCCAG | 105670 |
| rs254932832 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73173377 | GAACTCAGAAATCTG[C/T]CTGCCTCTGCCTCCC | 105670 |
| rs254970776 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73153323 | TTAAAGAAAATGAGG[A/T]TTCCAGCAGATCTGC | 105670 |
| rs254978973 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159706 | ACCTTCAGGTAACAG[A/G]CCAGATAAAAAGCTA | 105670 |
| rs255018686 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73170324 | GAGGATGGGGTGCCC[A/G]TAGCTTCCGGGCTCT | 105670 |
| rs255132756 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179014 | AAATGTTTTCATAAC[A/C]TACAATAAAGCAAGT | 105670 |
| rs255143041 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141937 | GCTGAACTTTCAGCC[C/T]CAGGAACCGTGAACT | 105670 |
| rs255227550 | snp | A/G | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73140522 | GTCTTCTTGTCTGAA[A/G]TCTCTAGATATACAT | 105670 |
| rs255322431 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73170223 | TGATGAAGAATGAGA[A/G]CACATCTTTCCACTG | 105670 |
| rs255352302 | snp | C/T | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73138299 | ACTCATAGAAACCCA[C/T]TGCTTTCTGACCTAT | 105670 |
| rs255472462 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169794 | TCCCTACTGTCAGGC[A/T]TTTCATCAACGCTCC | 105670 |
| rs255491582 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160290 | GCCTAATGGGATTGG[A/G]CCTAGTATTCCTTGT | 105670 |
| rs255547778 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73176159 | TGCCTTGGGGTCTAC[A/C]ACAGTGACTTGGCTT | 105670 |
| rs255642205 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73176715 | TTGGTGGGAACTGCC[C/T]ACTGGAACCACCCTA | 105670 |
| rs255661242 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144894 | GACTGGCCTGAACAA[C/T]GTGTCAGGGTAGCCC | 105670 |
| rs255663176 | snp | A/C | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152169 | CAGCTATAACCCCCC[A/C]CCCACACACACACAC | 105670 |
| rs255736998 | in-del | -/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160324 | GTGTCGATAAAGGGA[-/T]TTTTTAAGGCATAGG | 105670 |
| rs255758028 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73145410 | TATTCTTACGGTATA[C/G]CTGCAGGGAATGCTC | 105670 |
| rs255762592 | snp | A/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73140776 | AAATTTGTACAATCA[A/T]TAGTCAAAGAGCATT | 105670 |
| rs255834531 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73150649 | GTGCAGACTGACTGA[A/G]TCATTTGTGTGCCTT | 105670 |
| rs255839190 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73151215 | TTTACATGGTGAATT[C/T]CAGGTCAGTCAAGGC | 105670 |
| rs255916210 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73166945 | TCAGCTGCTGGGATG[C/T]TTCTGCTGAAGTAAA | 105670 |
| rs255971881 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73157756 | CAAGCATCTAGCTGT[C/G]TCACAGATTTGAAAA | 105670 |
| rs255973075 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73161024 | CAACTTCGCACACTC[A/G]AGACTCTTACCCGAG | 105670 |
| rs256016949 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181793 | TTGTGCTGAGTCAGA[C/T]CATACCTGGGTGTAG | 105670 |
| rs256111195 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141489 | TTAAGAGGTTTATTA[C/T]TGAGTGAATATAGCC | 105670 |
| rs256113361 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148667 | ACTGTGGTCCCCACT[A/G]CTGGGACCAACTTAC | 105670 |
| rs256208423 | in-del | -/CTAGCTTGCTT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73157309 | TTTACTGGCTTGCTA[-/CTAGCTTGCTT]CTGACTTGCTTCTGG | 105670 |
| rs256261196 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178047 | TTATCTGGTGCTGGA[A/C]CTGAAGGCAGGCTTG | 105670 |
| rs256303121 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73161296 | TTACAGACCCAGAAC[C/T]CCTTGGATGAAGGGA | 105670 |
| rs256308784 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147956 | CTTGTTTGTAAGTAA[C/T]GTGCCACGCTGTGCT | 105670 |
| rs256312598 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73162902 | TTGCCTTAGCAGTGG[A/G]GCGAGAACAGTCTCT | 105670 |
| rs256315380 | in-del | -/A | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73153615 | CCACTTCCAGTTGAG[-/A]AAAAAATTACAAATT | 105670 |
| rs256337081 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73183211 | GGAAGAGGTTGAAGT[C/T]GAGAAAGAAGAAGTA | 105670 |
| rs256362049 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73180393 | CAGGACAGGTGTTTC[A/G]GGAGTTGAGAAAAAT | 105670 |
| rs256399403 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73174195 | TAGTGAAACAGTTGG[A/G]AACATTTTTGGCTTT | 105670 |
| rs256405734 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73157859 | GGAAGGAATGGTGGT[A/G]TCTTATTTTATGTCT | 105670 |
| rs256412676 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177669 | GGTTGAAGACCAGGT[A/C]ATGCCCAGGGAAAAT | 105670 |
| rs256555763 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73167433 | GATTATAATCTGTGT[C/T]ATCACACCCAGGTTA | 105670 |
| rs256563847 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73168785 | TCTGGCTTCTTTGGA[C/T]AGTCACGTAACTGTC | 105670 |
| rs256576892 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73155045 | CTAGGATGTGGATGG[A/G]GCTGATGTCACCTAG | 105670 |
| rs256594079 | in-del | -/A | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73154487 | CTTCCTTGTAGACAG[-/A]AGGACCTCTGTTTCT | 105670 |
| rs256636056 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73175093 | AACACAGCCCTGCAG[A/G]CAGCCCTGAACACAG | 105670 |
| rs256640245 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73167746 | GTTTTTTATAACAGT[A/G]GTGAATGCTGTTGGA | 105670 |
| rs256671984 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73180517 | GAGAGAATGGAAGCG[A/C]GGAACTGGCAATGGG | 105670 |
| rs256692512 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73161022 | GACAACTTCGCACAC[G/T]CGAGACTCTTACCCG | 105670 |
| rs256727197 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73153973 | TGCTGGGATTAAAGG[C/T]GTGCGCCACCATGCC | 105670 |
| rs256773678 | in-del | -/T/TTT/TTTTT | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73171810 | TCTCCCTACCTTGAG[-/T/TTT/TTTTT]TTTTTTTTTTCCCCT | 105670 |
| rs256797842 | snp | A/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73174123 | AAAGCTGTCTTTCAG[A/T]TAAAAAATATATCTA | 105670 |
| rs256830525 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73170505 | TCTGAGCTTACACAG[C/T]GTCAGGCAGGCCTCG | 105670 |
| rs256965537 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148798 | ACTCCTGGAAGCCAG[G/T]ATAGAGCAGAAATAG | 105670 |
| rs256978928 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177758 | AGTAACAGAGTGCCC[A/G]GGGTCAGAGCATGTA | 105670 |
| rs257027473 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177932 | ATGAGACTGCTCTCT[A/G]AGAGACTGCTCTCCA | 105670 |
| rs257149915 | in-del | -/TTTC | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73171818 | ACCTTGAGTTTTTTT[-/TTTC]CCCTTAAAAATACAA | 105670 |
| rs257164411 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73140086 | CGCTGTAGTGATGAT[C/T]CTTTGATGTGTTTCC | 105670 |
| rs257192503 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73146854 | AAACTGTAACTCTCC[C/T]GGTAGAGCTGCCTCC | 105670 |
| rs257302994 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158820 | AATTGAACAGAGGGA[A/G]ACAGCCATTGCTGTT | 105670 |
| rs257345713 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73146052 | TCAGGAATCATGTTG[C/T]TGAGCCAAGTCTTTA | 105670 |
| rs257395361 | in-del | -/TA | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73142243 | ACATACATATATATG[-/TA]TGTATATATTTATTA | 105670 |
| rs257398069 | in-del | -/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73153437 | TTTAAGTGGTCTCTC[-/T]TTTGGTTTTAGTTTT | 105670 |
| rs257458004 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163838 | ACTGCCACACTTGGG[C/T]TGGGGACAGCACCAG | 105670 |
| rs257554082 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73150473 | CCTCCAAACACTGCT[A/G]CACTTGGGACCACAC | 105670 |
| rs257590957 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73176318 | ATCAGTAAAGACAGT[C/G]TGAGAAGGAGGCCAG | 105670 |
| rs257651692 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73161388 | TGCTCTTTAAGACCC[A/T]CCTTCCCCAGCCTCT | 105670 |
| rs257685466 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73180120 | CAGTCTTACTGTGTG[A/T]TGGAGCGTGGCAAGG | 105670 |
| rs257733803 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181731 | TAAATAGCTTCAACA[A/G]CAGAGACAGAATTTT | 105670 |
| rs257816072 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73150584 | AAATAAATAAATAAA[C/T]AAACAAATGATGTTG | 105670 |
| rs257854488 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73155915 | TATTGTTTTGCATCC[C/T]GTATCTTTTAGATAT | 105670 |
| rs257968230 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160698 | GTTTCAGTTGCTGCA[A/G]CCAAGCACCATGACC | 105670 |
| rs258095309 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73161420 | TCTGCTTAACTAGCC[C/T]GTTTCTATAGCTACA | 105670 |
| rs258106272 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178776 | AATGACTCTCAGGCC[A/G]AGCCTCACAGTGTGA | 105670 |
| rs258126369 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73173520 | TGTTATAAATGCCAC[C/T]AAAGTATGGTTCCAG | 105670 |
| rs258218459 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159075 | TAAAAGTGTCTCCAG[A/T]GTACAGACAATTGAA | 105670 |
| rs258239414 | in-del | -/GGA | | | intron-variant, cds-indel | Rcbtb2 | Mm_Celera | 14:73143720 | GCTGAGGCCGGAAGT[-/GGA]GGAGTTTAGAGGTGA | 105670 |
| rs258351643 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73145939 | AGCTAACAAGTGCTG[A/G]TGAATGATAGCTAAA | 105670 |
| rs258358656 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148042 | GTGCGAAGTATTCAC[A/G]CTATTCTCTTAAGGA | 105670 |
| rs258361119 | snp | G/T | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73138581 | GACTGCATGTGTGTG[G/T]TTCTAATGGTCTGTA | 105670 |
| rs258391134 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177355 | CGCAGACTTCCCTTG[C/T]CACTACTACATATGA | 105670 |
| rs258419503 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73178082 | GCTGAGCTTGTGCAC[C/T]GTGTCACTGCCCACT | 105670 |
| rs258430570 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169970 | CATTGCTGAACTGGT[A/G]TAGTTTCCAAAGAGA | 105670 |
| rs258442525 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73139437 | TCAAAATAATATTTT[G/T]ATTAGAACTTTTAAG | 105670 |
| rs258478580 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73145477 | ATTTCAGCTTTAACA[A/G]AGCTGAAGAGAAGTT | 105670 |
| rs258508228 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73166119 | CTCCCTCAAATTCAG[C/T]TTTATTCTTGGTAGC | 105670 |
| rs258577230 | snp | A/C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73171584 | TGCTGTCTTACCCAG[A/C/G]AGAGCTGGTAGACTG | 105670 |
| rs258650384 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73162674 | GTAGGTAACACACGG[A/G]GCCTAAACGGCTGCA | 105670 |
| rs258652762 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73156989 | GGCAGTGGAAAGGAG[A/G]TGAATTAAGTAGTAT | 105670 |
| rs258661971 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73153841 | ACTAAAGACAGCTTC[A/G]TTTGTTTTTTGTTTT | 105670 |
| rs258674391 | snp | A/G/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73158164 | GCCATTGAGGACTCT[A/G/T]TGAGCGTGGTGTACT | 105670 |
| rs258680097 | snp | A/G | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73140821 | GCTGTTTCAGGCACA[A/G]GGAAGAAAGAGCTGA | 105670 |
| rs258732366 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73171108 | TTCAGCCATGCAGTA[C/T]GGCAGGGCCAGAGTG | 105670 |
| rs258763162 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73152062 | TTGCAGAGAATAAAT[G/T]AAGCGCACTCTAAAT | 105670 |
| rs258790931 | in-del | -/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147238 | TAAATAGCCTCAGGG[-/C]CCACAGTTTGATCAG | 105670 |
| rs258857769 | in-del | -/GAAGCG | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177964 | GAGTGATGCTGAAGC[-/GAAGCG]GGGCAGAAAGATGGG | 105670 |
| rs258900972 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163716 | TCTGCAGGTGGCGGA[C/T]ACTCTTCTGTTTGGG | 105670 |
| rs258947076 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73151882 | GCTTGTGACTGATGG[C/G]TGGCAGGTTGGACAT | 105670 |
| rs258951966 | in-del | -/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73162105 | ATGAGGTAATTTGGA[-/G]AGAAAAAATTCAACC | 105670 |
| rs258968113 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73168840 | ATGACACATAAACAT[C/T]ACACTACTTCCCCTA | 105670 |
| rs259000958 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163346 | AGGAGAAGACTGAGT[A/T]AAACCATCCCTGAAT | 105670 |
| rs259012835 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73175753 | CCTCTTTCCTTCCTA[A/G]CATGATGATCTGGGA | 105670 |
| rs259067422 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147715 | TAAATTTTCTTCTGA[A/G]ATTACTTCTCATAGA | 105670 |
| rs259074475 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73168454 | GTGCTGTCCTGTGCA[A/G]ACTACAGTGACTGAA | 105670 |
| rs259121956 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144277 | AGAGACCGAGTTCAC[A/G]GTCCTGTGGAACTTG | 105670 |
| rs259172391 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73154708 | GACTTCCTTTGTTGC[C/T]CCGGTGTCTCTAATT | 105670 |
| rs259225124 | snp | A/C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73175326 | AGCCCTGAACACAGG[A/C/T]CTGCAGACAGCCCTG | 105670 |
| rs259259270 | in-del | -/GGGGGGGG | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165123 | TTTGTTTTTTTTTTT[-/GGGGGGGG]GGCTTTCAGTCTACA | 105670 |
| rs259305582 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73168478 | GACTGAACTGTCACT[C/T]GCAGTTCTGTGGCTG | 105670 |
| rs259314981 | snp | A/G | | | intron-variant, utr-variant-5-prime | Rcbtb2 | Mm_Celera | 14:73143432 | GTGCGCATGCGCGCA[A/G]GCCCAGCCCGGGGTC | 105670 |
| rs259399350 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178868 | GTGCTGTGACATGCA[C/T]CATGGACAAGCTCCA | 105670 |
| rs259457142 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73149534 | TCCCTTGCAGCTGGA[C/G]TGCAGACAGTTGTGA | 105670 |
| rs259479431 | in-del | -/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73154125 | AGCTCCTGTTGTCAC[-/T]TTGATGGGACAGCGG | 105670 |
| rs259513107 | snp | C/G | | | intron-variant, utr-variant-5-prime | Rcbtb2 | Mm_Celera | 14:73143465 | TTTTGTGCGTCGCCC[C/G]GAGGCCACGGCTGTG | 105670 |
| rs259535051 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178229 | ATTTCTAGGAAAAAT[G/T]ATTCAAGCCATTCTG | 105670 |
| rs259558946 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73140858 | TAAAGCGTCGCCTGC[C/T]CTTTTGGGGGAGGGG | 105670 |
| rs259662473 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73140395 | TCCACAAACGCCTTT[A/G]ATTTTAATTTCAGTT | 105670 |
| rs259690979 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73153267 | AGAGAGAAGCCTATT[A/G]GGTGAGTCAGGAGGC | 105670 |
| rs259729815 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165083 | GGGAAGAAAGAGGTT[G/T]TTGGGTTTTTTTTTG | 105670 |
| rs259781186 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73146582 | CAATTTTATTGAGGC[C/G]TAGACTGTTTTCAGC | 105670 |
| rs259813829 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73176689 | TGGGGCCTCCTGAAA[A/G]GCACCATATCTTGGT | 105670 |
| rs259841298 | snp | A/G | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73140877 | TTGGGGGAGGGGTTC[A/G]AATGTTTTCTCTTTC | 105670 |
| rs259926116 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73171212 | TTAGCTGAAGCAGTG[C/T]CCTGCCCTGGGTCCT | 105670 |
| rs259929809 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73176101 | GCATGACACGTAGCA[G/T]TCTCCGAGTCTGCCT | 105670 |
| rs260002245 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181077 | TTTATTTAATCCCAT[A/G]AACTCTTTCTGAATT | 105670 |
| rs260030895 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144511 | TACTTTCAACTCTTA[A/C]CTATACACTGGGAAG | 105670 |
| rs260049930 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73174906 | AATAAGCCATGGAAG[C/T]TCTGGCTGTAGCTTA | 105670 |
| rs260077528 | in-del | -/AGGTGC | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73166983 | CTTCCCCTGAACTAA[-/AGGTGC]GATCTTCAGGGAGAT | 105670 |
| rs260095724 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181566 | GGGGAAATCTCCTAT[A/G]GGTTCGTGTACATGT | 105670 |
| rs260123518 | in-del | -/TTA | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73154006 | GCTCTAGATACAGTT[-/TTA]TTAAGTTGACTTTCA | 105670 |
| rs260150509 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73146211 | TATTTTCCCACTTGA[C/T]GGTGACGTTTTGTCA | 105670 |
| rs260182318 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73182910 | TCCCTCTCCCAGCAC[A/G]TGCCAACTGTAAATA | 105670 |
| rs260195059 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73139837 | GATGTGCTTAGGTCA[C/T]AGGGAAGGGATGAGA | 105670 |
| rs260218414 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73149169 | ACAGCGAGCCGATCC[C/T]GCTGATTGGAAAAGT | 105670 |
| rs260326871 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73182132 | TATAAACTCTTCACA[A/G]GCAGAAGCATTTAAA | 105670 |
| rs260427096 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169839 | TGGGAATAACATGGT[C/T]AATCTTATATAACCT | 105670 |
| rs260478603 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73173105 | TGTAAAGTACCTGAT[A/G]GTTTGGTTTTGGTGA | 105670 |
| rs260509696 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73180269 | TAGAGAGAAGTGTCC[C/T]GAGAGCTGTAAGAGG | 105670 |
| rs260563493 | in-del | -/AAAAAA | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73174125 | AGCTGTCTTTCAGAT[-/AAAAAA]TATATCTAGAAACAG | 105670 |
| rs260625933 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73142685 | TCCTTCATTTTAAAG[C/T]CGGACAGCTCTCTGG | 105670 |
| rs260652673 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179890 | GCAACTGTATCCACA[C/T]GGAGTAGGCTGGCTG | 105670 |
| rs260663208 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73155975 | GTTTCACATATTTCA[A/G]CCTGCCTATTGATTG | 105670 |
| rs260755155 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160662 | AAAACAAGGCCCATA[A/G]AGGCCTGTGTCTCAG | 105670 |
| rs260787760 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73155111 | TGGACTTCTTAAGGA[C/T]GTTAAGTGTCTCTTC | 105670 |
| rs260792190 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160778 | GATTATAGTTCATCA[C/T]TGGAGGAAGTCAGGA | 105670 |
| rs260818249 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73170548 | TGGCAAGAAAGAAAT[A/G]TGTAATCTGCTAGGA | 105670 |
| rs260882403 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160472 | CAGCACATTTGAAGA[A/G]CTTTGTTGTTGCCCT | 105670 |
| rs260891692 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73166462 | TCGCTTTGTTTATCA[A/G]TCTTTTCTTTCCCAT | 105670 |
| rs260931901 | in-del | -/ACTAGTAAAT | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73183819 | GTTTCTTAACCAGGC[-/ACTAGTAAAT]ACTAGATAGAAAGGA | 105670 |
| rs260945821 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73145748 | CTTATCTGGAAGAAG[C/T]ATGTGTCTCTTTCAG | 105670 |
| rs260976586 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73152899 | TTGACGTTAAATATG[A/G]AAAAGGTATTTCCAG | 105670 |
| rs261028369 | snp | A/C | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141150 | ATTTGGTCTCAAAAT[A/C]CTTTTTGTGTGTATA | 105670 |
| rs261067100 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163615 | CCTTTCCTTGCTGAT[A/T]TAGAGTCGGCCAGTA | 105670 |
| rs261113015 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158995 | CATTCGAGGCACCAA[A/T]GGAGTCATGATGGGA | 105670 |
| rs261116961 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147531 | TCTCCTGCACCGCCT[G/T]CCTTTGACTCAGTAA | 105670 |
| rs261176892 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73146648 | TAGTTCTTTCTGATT[A/G]CAGGCTGGCTGATTC | 105670 |
| rs261191999 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169382 | GTGTTTGAGAGATTT[C/T]GAGAGTCCAGATTAA | 105670 |
| rs261203330 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158509 | CCGTTATCTGTGAAC[C/T]AGCTTTCAGCAAGTC | 105670 |
| rs261219545 | in-del | -/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163204 | GAGGGTTACAGGTTA[-/C]AGGTAGCTGGAGTGG | 105670 |
| rs261304714 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163640 | CCAGTACTTCTCTCC[A/G]TTAAGTGCCTGCTTC | 105670 |
| rs261314650 | in-del | -/GTAAAGGAGCTTGCT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178772 | TGAAATGACTCTCAG[-/GTAAAGGAGCTTGCT]GCCGAGCCTCACAGT | 105670 |
| rs261317027 | in-del | -/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73167948 | AGTGATGAAACATTT[-/C]CCTGTTACTTGTAGA | 105670 |
| rs261366326 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147450 | ACTCTGTGAACACGT[G/T]TGGGGACCCCCATGG | 105670 |
| rs261386613 | snp | G/T | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137097 | TTTTGTTTTGTTTTG[G/T]TTTTGCTGTTAGAGA | 105670 |
| rs261419453 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144562 | TGGCAGTGCTGTAGG[A/C]CTCAGGATGGAGCAT | 105670 |
| rs261433107 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181431 | GACTATTCCGTTTTG[C/T]CTTCAAGAGCTCATG | 105670 |
| rs261435709 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73140890 | TCAAATGTTTTCTCT[C/T]TCCTCCAGCTTTACA | 105670 |
| rs261450406 | snp | A/G | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137454 | CTGGCTGCCCAGAGT[A/G]AACTATTGCTCCCGA | 105670 |
| rs261550110 | in-del | -/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179445 | GGGATTCTAAGTCTG[-/T]CGGAGGAAACAATGC | 105670 |
| rs261606361 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73171027 | CAAAACAAAGCAGCA[A/G]CAACAACCCCCCCCC | 105670 |
| rs261667887 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73162509 | GGACAGGTTTGAAGC[A/G]TTGCTTATTTGTTAA | 105670 |
| rs261717011 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73139602 | CAATTTTATTTTCCT[G/T]GTTAATTATTCTATT | 105670 |
| rs261776851 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163251 | TACCCTGGGACTGCA[A/T]GGCCAGACCCTCAGC | 105670 |
| rs261791542 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73157987 | GGAATCTTCCTGTTC[A/T]GAGACTCATGACCTG | 105670 |
| rs261801112 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160178 | CATTGAACAGAGATT[C/T]TAGATTTACTATTAA | 105670 |
| rs261919253 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144236 | CCATCCTGATAGAAC[A/G]GTTTTGGCGATTAAA | 105670 |
| rs261953797 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73180798 | GGTTTCTAGCAAGAG[A/G]CAGAAGTGAGGGGAA | 105670 |
| rs261963474 | snp | A/G | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73142207 | TAAACTGATGTGTGT[A/G]TATATATATATATAT | 105670 |
| rs262002499 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178187 | TGACCCAGGAGAGGG[G/T]AATTCAGAGAAACAC | 105670 |
| rs262044230 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73139317 | CGTGGTACTTTTTAA[A/G]TACTGAGGACTTAAA | 105670 |
| rs262099050 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73161382 | GAGATATGCTCTTTA[A/C]GACCCTCCTTCCCCA | 105670 |
| rs262124746 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73182865 | CACATAGAAGCTGAA[A/C]GTGTACCAGTGCCAC | 105670 |
| rs262131722 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73166219 | CTTAAAAGGGCCCAT[C/T]ATTACTTTTATATTG | 105670 |
| rs262152533 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160514 | CAGATCTTAGGGTTG[A/G]AGATGCTGCTGCACA | 105670 |
| rs262211695 | snp | A/G | | | downstream-variant-500B | Rcbtb2 | Mm_Celera | 14:73184111 | AACTTTTGTCTCACA[A/G]GTGGATAAAAATCCC | 105670 |
| rs262219550 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158310 | GAGAATATATAAAAA[A/C]CACAGAAGGCCACTA | 105670 |
| rs262228839 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73140346 | TGATTTTATGTTGAC[A/T]TTGTAACTGGATATC | 105670 |
| rs262254413 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73180599 | ACAGATTGAAGGGCC[A/G]GCTGAGATAATCAAT | 105670 |
| rs262290860 | in-del | -/TT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165099 | TTGGGTTTTTTTTTG[-/TT]TTTTGTTTTTTGTTT | 105670 |
| rs262357237 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73164184 | CACATGTGATTGATT[C/T]ATTCAAAGTGCAGAA | 105670 |
| rs262425122 | in-del | -/TTG | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137081 | GGTTTTGTTTTTGTT[-/TTG]TTTTGTTTTGTTTTG | 105670 |
| rs262434016 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181965 | TCACCTGTACTAAGC[A/G]CACAGTCTACTGCTT | 105670 |
| rs262445501 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73161233 | TTACATTGGGTTGCA[C/G]TAATGGGGATTCATG | 105670 |
| rs262604167 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73173975 | AGGAAGGTACTTTTG[C/T]TGTGCGACCTTAGGA | 105670 |
| rs262614965 | in-del | -/G | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137658 | TCAAAGCTATTATCT[-/G]GGGTTCGCCTGGACT | 105670 |
| rs262657583 | in-del | -/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73161392 | TTTAAGACCCTCCTT[-/C]CCCCAGCCTCTGTCT | 105670 |
| rs262708932 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179082 | TTGACTGGGAGAAAA[A/G]TGAACCAAAGAACGA | 105670 |
| rs262811978 | snp | A/T | | | utr-variant-5-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73154326 | CCAGCTTAGCAGATC[A/T]TACATTCTTCAGGAG | 105670 |
| rs262829079 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73176604 | AGGTTATTTGCTTAC[A/T]TGGTGCGGCTGAACT | 105670 |
| rs262864215 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160023 | GACCGCATTGTACCA[C/T]GGGAACCTAATGGGC | 105670 |
| rs262940616 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178103 | ACTGCCCACTCCCAA[C/T]CCAACCGGCTTTCTT | 105670 |
| rs263007549 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73157901 | ATTCGATCTTACCTG[A/G]CATTTCCCTGCTCAG | 105670 |
| rs263036107 | snp | A/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152193 | CACACACACACACAC[A/T]CACACACTGCATCCC | 105670 |
| rs263090590 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73174633 | TGCTGTTGTGGGTGT[A/G]TGTCACACTAAATAG | 105670 |
| rs263141897 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73155746 | TGATGCTGTTTCCCA[C/T]GCAGTATCCAGTGAT | 105670 |
| rs263152333 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181486 | CTGAGACTCCAGCAG[A/C]CTGCCAGTCTGTTAT | 105670 |
| rs263170163 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73176079 | TGGCAATCTTCCTCT[C/T]TCTGAGGCATGACAC | 105670 |
| rs263189547 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148477 | AACTGTTTGCAGAGC[A/G]TACTATGGACTATGT | 105670 |
| rs263278021 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73150266 | GCCTTTTTGGGCACT[A/G]GGCCAATGTATGTTT | 105670 |
| rs263327143 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73157526 | CATTTCTGGAACACA[G/T]AATGGTTGACACATG | 105670 |
| rs263346111 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73172090 | AGAGCTAGTGTTGTG[C/T]CCAAACCAGGATGCT | 105670 |
| rs263402424 | in-del | -/TGTT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73173264 | GGGTTAAACATTGCA[-/TGTT]TGTTTGTTTGTTTGT | 105670 |
| rs263448158 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147213 | TTTTTTTCTCTTTCT[C/T]TTTTTTCTGTAAATA | 105670 |
| rs263463624 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177992 | AAGATGGGTTGGAGG[A/G]CAGGAGGCAGATGTG | 105670 |
| rs263481490 | snp | A/C/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73153474 | GCAAATGGTCTGCCC[A/C/G]CGAATTTCACCTTCA | 105670 |
| rs263527647 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73146957 | TCGTGAGTTGGGTGT[A/G]TTCTGTCTCTGACTC | 105670 |
| rs263639378 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73168735 | GTTTTATGAACTGAC[A/G]TAATTTCCAAACGAT | 105670 |
| rs263650834 | in-del | -/A | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179324 | GCTTCCTCTTGGCAT[-/A]AGGATAGCCTCCCTC | 105670 |
| rs263690872 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144185 | AGCCTGATACCTGAA[C/G]GGAGAGGCGAACATG | 105670 |
| rs263699308 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177538 | ATGTCTGCTACACTC[A/G]GCTGTGAAAGTGGGC | 105670 |
| rs263721037 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73170263 | GGAGCAGACTGTGGG[C/T]CACTAAAGTGGAGGA | 105670 |
| rs263775856 | in-del | -/TGGTGTACATGCAT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158212 | TTTTGCTCAGCACTC[-/TGGTGTACATGCAT]GGGCCTTTGTTCTCC | 105670 |
| rs263842036 | in-del | -/GTT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73171809 | CTCTCCCTACCTTGA[-/GTT]GTTTTTTTTTTCCCC | 105670 |
| rs263859234 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73167231 | TATATAATTAATATG[C/T]ATTAAAAGCTACAAT | 105670 |
| rs263869040 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73168203 | GGAATTCATAGTGTA[C/G]AATTGTGGGAAAGTA | 105670 |
| rs263939191 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73173831 | GTCGGTGATCCTTCC[A/G]CACCACACTCACTTC | 105670 |
| rs263941462 | snp | C/G | | | intron-variant, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73143160 | GCAGTCCCCGCTGCC[C/G]GGGAGCGGAAAGGAC | 105670 |
| rs263951970 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73173565 | AAGTTTAGGAAGTGA[G/T]TTGTCCAAGTCTTGC | 105670 |
| rs264036359 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148045 | CGAAGTATTCACGCT[A/G]TTCTCTTAAGGATTA | 105670 |
| rs264105184 | in-del | -/A | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73142583 | TTTTCAGTGCTCCTT[-/A]AATGAGATCCGTAAG | 105670 |
| rs264121467 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152462 | TCCTTATGCTAGGCA[C/T]ACAGTTACATTTTTA | 105670 |
| rs264135062 | in-del | -/AAATGGTTAGAATTTACAACTTGATTCTTAGTATCCAGAAAGCCACTTGATTTTGTAGCAAGGGCCAGGATAAAATCTCA | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73158074 | AGACAAGTGTTTAGG[lengthTooLong]AAGCATGCTTGAAAG | 105670 |
| rs264145138 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73170102 | TTGCTAAAGGTCACA[C/T]GGAGGCAGTAAGGAC | 105670 |
| rs264221597 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73156349 | GGTTCTCAAACTCTT[A/G]GTTCACAATCGTCTA | 105670 |
| rs264280468 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73146035 | TCGAGGATCCACTGT[A/G]TTCAGGAATCATGTT | 105670 |
| rs264314453 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158998 | TCGAGGCACCAATGG[A/G]GTCATGATGGGAGAG | 105670 |
| rs264357834 | in-del | -/AG | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73162717 | AGCCCTTCTGTTCTC[-/AG]AGAGTGGAATCATTG | 105670 |
| rs264420411 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169739 | ATGAGACTATGGGAT[A/G]ACAACCCCATCCCTC | 105670 |
| rs264475873 | in-del | -/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73155112 | GACTTCTTAAGGACG[-/G]TAAGTGTCTCTTCAC | 105670 |
| rs264533866 | snp | A/G | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141466 | CCACCCCGGGCTTAG[A/G]TATACTCTTAAGAGG | 105670 |
| rs264578062 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73151175 | CTTATGTACTCGGGG[A/G]CAGAGCAGGGGATCT | 105670 |
| rs264581042 | in-del | -/TG | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73182320 | GAAACATGGACTAAT[-/TG]TGTTAATAATTGCTG | 105670 |
| rs264603483 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73155773 | TGATGCTGTTTCCCA[C/T]GCAGTATCCAGTGGA | 105670 |
| rs264671063 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165373 | GAATGGGCCATGCCA[C/T]ATCAATCATTAATCA | 105670 |
| rs264681193 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159904 | CTTCCTTTGCTTCCC[A/G]TAGCAGATTGGGACT | 105670 |
| rs264714470 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73140239 | TCAGCTCGTATTCCA[C/T]TGGGTTTGTGGATTC | 105670 |
| rs264718290 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73170325 | AGGATGGGGTGCCCG[A/T]AGCTTCCGGGCTCTG | 105670 |
| rs264724285 | in-del | -/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159946 | ACCTTGTGGGCTGAG[-/T]TAACTACTGCTTGTC | 105670 |
| rs264761810 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73183980 | AATATGATACTATGT[A/T]AAGGAAATCTTTTTG | 105670 |
| rs264842226 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73180317 | TACAGAAGTACCATG[C/G]GAAAGCCACTTTTAA | 105670 |
| rs264929779 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160909 | CTTTCTTACAGAACA[C/T]AGGACCACCAGCCCA | 105670 |
| rs264959842 | snp | C/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73166890 | ACGTCTCCTGGGGGG[C/G]GGGGGGCGGTGCACC | 105670 |
| rs265038683 | in-del | -/ACTA | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141592 | TGACTTACTTATAAG[-/ACTA]ACTTTCTTACATTGT | 105670 |
| rs265046040 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159305 | TCCAGTCTGACTTGG[A/G]TGTTTCTCAGAAAGG | 105670 |
| rs265056343 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163767 | CTGTCTTGGTCTCTC[C/T]GGTCAGATGACAGCG | 105670 |
| rs265070254 | in-del | -/TA | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73142208 | AAACTGATGTGTGTG[-/TA]TATATATATATATAT | 105670 |
| rs265086793 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177490 | AGAGCCCTAGAAGAT[C/T]TCTTTGTCATTGCCC | 105670 |
| rs265148456 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181708 | ACTGTTGGGAGCTTT[A/C]TATTTTATAAATAGC | 105670 |
| rs265217390 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179798 | CTTGTATATATTTTT[A/T]AATTCTTAAAACTTG | 105670 |
| rs265227435 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73173479 | GCATATATTTTTAAG[A/G]CCTACTGGTAATCAA | 105670 |
| rs265304496 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160322 | TTAGTGTCGATAAAG[G/T]GATTTTTAAGGCATA | 105670 |
| rs265380276 | in-del | -/TATA | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148560 | TCACCTGCTATGGAG[-/TATA]TATATATATGAGCCA | 105670 |
| rs265401590 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178305 | TTCCCGGGGTGCTGT[A/G]AAGGCGGCTTCAGAG | 105670 |
| rs265449015 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158074 | TAGACAAGTGTTTAG[A/G]AAGCATGCTTGAAAG | 105670 |
| rs265489056 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73175171 | GCCCTGAACACAGCC[C/T]TGCAGACAGTCCTGA | 105670 |
| rs265520015 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73180939 | GAACAGAACTAAGAG[C/T]TCTTATTAAAAGGTG | 105670 |
| rs265584917 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73149334 | GAGGATTGTTTTCTC[A/G]GTGCCCTTAAACTTT | 105670 |
| rs265650438 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147393 | TTACATTACCTGTAA[C/T]TCGGGGATGACACTA | 105670 |
| rs265660361 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158146 | GCCAATGCATGGGAA[A/G]CAGCCATTGAGGACT | 105670 |
| rs265782504 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73177088 | CCGAGCTTTCCTGGA[A/G]TATCTATACACAGAT | 105670 |
| rs265857420 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73174073 | ACTAACACAATACTA[A/G]TTAGAGGTAATTTGA | 105670 |
| rs265868030 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73167649 | TGTTTACACGTTTCT[C/T]CATTTTCCACATTAA | 105670 |
| rs265912344 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73142140 | GATGGATTTGAGTCA[C/T]CTCTAATCATATGGC | 105670 |
| rs266027061 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73172411 | AAAGCTGTGCAGCGA[A/T]GAGTTAACCAAACTG | 105670 |
| rs266037104 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73145600 | GAATCATGAGTGTGG[C/T]AGAGGGGCATTAAAG | 105670 |
| rs266135474 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163370 | CCTGAATTCGCAGCT[A/G]TAGATCTGTGTCACA | 105670 |
| rs266224435 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73155611 | TGATGCTGTTTCCCA[C/T]GCAGTATCCAGTGAT | 105670 |
| rs266226398 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144339 | TTTAACGGTCATTGA[G/T]TCCGCTCTGTATTCG | 105670 |
| rs266252814 | snp | G/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73156681 | ACAAAAGGTGAGGTA[G/T]TGCATGTATTTTTTA | 105670 |
| rs386927521 | in-del | -/CG | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73153475 | AAATGGTCTGCCCGC[-/CG]ATTTCACCTTCAGCT | 105670 |
| rs387001235 | in-del | -/AGAAGTCATTTTCTTTTTTTTTTTTTTTT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147018 | GTCTGCCACTCAATT[lengthTooLong]AGAAGTCATTTTCAA | 105670 |
| rs387247655 | in-del | -/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73151772 | TCGCTCGAAGACACT[-/T]TAAGTTACAAAAATG | 105670 |
| rs387469974 | in-del | -/TT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148856 | CGATATTCAACAATT[-/TT]TTTTTTTCCTAGCTC | 105670 |
| rs387630495 | snp | A/C | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152173 | TATAACCCCCCCCCC[A/C]CACACACACACACAC | 105670 |
| rs387752844 | in-del | -/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165339 | GGACCGCCAAGTCAG[-/G]GGTGGCACTGCTGCC | 105670 |
| rs578376127 | snp | A/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | GRCm38.p3 | 14:73141564 | ATGGCTAACCAAAAC[A/T]TGCCTACTTCTTTGA | 105670 |
| rs578381945 | snp | C/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73160965 | GGGCCCTCCCCCACT[C/G]ATCACTAATTGAGAA | 105670 |
| rs578391793 | snp | A/C | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73176428 | GCAATGTAGAGTCAG[A/C]TGCCTGGGCCACCTG | 105670 |
| rs578393676 | snp | G/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73169540 | CTCTTTTAGCTGCTT[G/T]TTGGGTCTTTCACAG | 105670 |
| rs578403939 | snp | C/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73155531 | GATACTGTTTCCCAC[C/G]CAGTATCCAGTGATG | 105670 |
| rs578547668 | snp | A/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73153153 | TCTAGTAACAAAGGG[A/T]TGTGGTCTCCTCTCT | 105670 |
| rs578560325 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73155503 | TGATACTGTTTCCCA[C/T]GCAGTATCCAGTGAT | 105670 |
| rs578578553 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73162693 | TAAACGGCTGCAAGA[C/T]GATGCACAAAGCCCT | 105670 |
| rs578584493 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73179130 | TGAGAGAAGCAGGAG[A/G]TGATTCTGTCCTTAA | 105670 |
| rs578587769 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73169221 | GATGCCCCCACCTCC[C/T]ACCCCACCTGACCTC | 105670 |
| rs578742818 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73166972 | TAAAGGCAAAGCCTT[C/T]CCCTGAACTAAGGTG | 105670 |
| rs578756663 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73151369 | TTGCATTTTTATCAT[C/T]TTAATATTTTCTATT | 105670 |
| rs578781184 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73157707 | GTAATAGTTCCCTCA[C/T]GGATTTAAAAGATGG | 105670 |
| rs578829541 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73175073 | CAGCCCTGCAGACAG[C/T]CCTGAACACAGCCCT | 105670 |
| rs578987441 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73150568 | CATTAAATAAATAAA[C/T]AAATAAATAAATAAA | 105670 |
| rs578992335 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73165591 | CGCACACACATACAC[A/G]CACACACACACACAC | 105670 |
| rs579137873 | snp | A/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73158212 | TTTTGCTCAGCACTC[A/T]GGTGTACATGCATGG | 105670 |
| rs579139985 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73146396 | CTTCCCTTGACAGTG[C/T]GCTGGCTTTCCCATT | 105670 |
| rs579143973 | snp | C/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73175142 | ACACAGCCCTGCAGA[C/G]AGTCTTGAACACAGC | 105670 |
| rs579163908 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73165586 | ATCATCGCACACACA[C/T]ACACACACACACACA | 105670 |
| rs579185375 | snp | G/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73150337 | AAATACATAGGGGTG[G/T]GTGTGTCACACACAC | 105670 |
| rs579352790 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73161637 | GATGTGGGTGACTCT[C/T]AGCAACACACAGCAT | 105670 |
| rs579397610 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73155452 | TGCTGTCTCCCACCC[A/G]GTATCCAGTGATGCT | 105670 |
| rs579399008 | snp | A/C/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73169195 | TCCCCACCCCACCCC[A/C/G]TCTCCACGTAGATGC | 105670 |
| rs579404427 | snp | A/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73143945 | GGGCCACTTGACGAG[A/T]TTGTTGTGACAATCA | 105670 |
| rs579466593 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73146367 | TGCACTCCTTTCCTA[C/T]GCACTGGGTGGCACT | 105670 |
| rs579486966 | snp | A/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73173326 | TGTGTAGCCCTGTGT[A/T]GTCCTGAAACTCACT | 105670 |
| rs579523925 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73162905 | CCTTAGCAGTGGAGC[A/G]AGAACAGTCTCTTGG | 105670 |
| rs579531331 | snp | A/C | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73179479 | GAGCAGACTATATGA[A/C]TGTTCTGTCCATGGG | 105670 |
| rs579535300 | snp | A/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73156443 | TCTCCCCCTCTCCCC[A/T]CCCTCCCTCCCTCCC | 105670 |
| rs579672837 | snp | C/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73159956 | CTGAGTTAACTACTG[C/G]TTGTCACCTGCCAGT | 105670 |
| rs579683354 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73175310 | AGACAGCCCTGCAGA[C/T]AGCCCTGAACACAGG | 105670 |
| rs579687377 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73155641 | TACTGTTTCCCACCC[A/G]GTATCCAGTGATGCT | 105670 |
| rs579721513 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73145397 | CGAAAAAAACTATTA[C/T]TCTTACGGTATACCT | 105670 |
| rs579901203 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73175241 | TAGCCCTGCAGACAG[C/T]CCTGAACACAGCCCT | 105670 |
| rs579931605 | snp | C/G | | | upstream-variant-2KB, intron-variant | Rcbtb2 | GRCm38.p3 | 14:73141307 | TCGTTTTGTTTGTTT[C/G]TTCGTTTTGGATTTT | 105670 |
| rs580015267 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73175206 | AGCACTGCAGATAGC[C/T]CTGAACACAGCCCTG | 105670 |
| rs580126637 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73159127 | TGGTCCTAGGAGAGA[A/G]GGGCATATGGTCATG | 105670 |
| rs580164790 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73167960 | TTTCCCTGTTACTTG[C/T]AGACTTGACTTTTTT | 105670 |
| rs580245892 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73172051 | AGTATAAATGATATG[A/G]CTTATACAGACTACT | 105670 |
| rs580357769 | snp | A/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | GRCm38.p3 | 14:73141318 | GTTTCTTCGTTTTGG[A/T]TTTTTGAGACAGGGT | 105670 |
| rs580448744 | snp | G/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73163257 | GGGACTGCAAGGCCA[G/T]ACCCTCAGCACAGGA | 105670 |
| rs580581498 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73155561 | GCTGTTTCCCACCCA[A/G]TATCCAGTGATGCTG | 105670 |
| rs580617305 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73150330 | TAAAATTAAATACAT[A/G]GGGGTGTGTGTGTCA | 105670 |
| rs580675511 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73165522 | AAATGAATCTATCTA[C/T]CTATCCATCTATATT | 105670 |
| rs580775981 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73155443 | ATCCAGTGATGCTGT[C/T]TCCCACCCAGTATCC | 105670 |
| rs580849059 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73169156 | CCCCATCCACCCTCT[A/G]ACTGCTCCACATCCC | 105670 |
| rs580894728 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73176468 | CAGCAGCAGCAGCAG[C/T]AGGCTGCATTTGCAG | 105670 |
| rs580952598 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73169135 | CATATTCCATTCCCC[A/G]CCCCTCCCCATCCAC | 105670 |
| rs581128846 | snp | A/C | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73176380 | GCATTGTAAAGTCAG[A/C]TGCTGGGCCGCCCAC | 105670 |
| rs581130385 | snp | A/C | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73160962 | GCTGGGCCCTCCCCC[A/C]CTGATCACTAATTGA | 105670 |
| rs581179992 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | GRCm38.p3 | 14:73141388 | AGACCAGGCTGGCCT[C/T]GAACTCAGAAATCCA | 105670 |
| rs581192126 | snp | C/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73175325 | TAGCCCTGAACACAG[C/G]TCTGCAGACAGCCCT | 105670 |
| rs581256295 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73160919 | GAACACAGGACCACC[A/G]GCCCAGGGGTGGCAC | 105670 |
| rs581256774 | snp | A/C | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73169214 | CCACGTAGATGCCCC[A/C]ACCTCCCACCCCACC | 105670 |
| rs581350206 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73156827 | CAGTAGATACAGAGC[C/T]TGTTTGTTCCAGACC | 105670 |
| rs581441457 | snp | A/C | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73175054 | CTGCAGACAGCCCTG[A/C]ACACAGCCCTGCAGA | 105670 |
| rs581529487 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73165587 | TCATCGCACACACAT[A/G]CACACACACACACAC | 105670 |
| rs581534294 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73146906 | CCCCTCCCCCTCCCT[C/T]TCTGCTGTTCCCTCT | 105670 |
| rs581609290 | snp | G/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73150339 | ATACATAGGGGTGTG[G/T]GTGTCACACACACAC | 105670 |
| rs581669319 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73156473 | CCCCTCCCCTCCCTC[C/T]CTCCCCCCTCCCCTC | 105670 |
| rs581675582 | snp | A/C | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73174243 | TGTTCAAAGGCGTGA[A/C]TCCATACCCAGAGGC | 105670 |
| rs581818074 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73167051 | TGGAAATGTAGGCTT[C/T]ACACCCTTTCCTGTA | 105670 |
| rs581906734 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73175075 | GCCCTGCAGACAGCC[C/T]TGAACACAGCCCTGC | 105670 |
| rs581913412 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73161170 | TGTGTTTCCTAGGAT[A/G]AAATAGATATGTTTA | 105670 |
| rs582027933 | snp | G/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | GRCm38.p3 | 14:73142256 | ATGTGTATATATTTA[G/T]TATATATAGCACAAT | 105670 |
| rs582074064 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73155546 | GCAGTATCCAGTGAT[A/G]CTGTTTCCCACCCAG | 105670 |
| rs582085958 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73169874 | AGATCTGTAAAAGGA[A/G]ACTTTTTAAGTTAAG | 105670 |
| rs582096792 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73169369 | GTTTGGTGGTCCAGT[A/G]TTTGAGAGATTTTGA | 105670 |
| rs582217052 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73155519 | GCAGTATCCAGTGAT[A/G]CTGTTTCCCACGCAG | 105670 |
| rs582230140 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73162694 | AAACGGCTGCAAGAC[A/G]ATGCACAAAGCCCTT | 105670 |
| rs582233855 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73179158 | TAAAGAGCACATACT[C/T]GCACGGGGCGATCAG | 105670 |
| rs582256330 | snp | G/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73144096 | GCAGAGTTGGCCTGG[G/T]CCAGGTTTGGTCCGG | 105670 |
| rs582262536 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73178317 | TGTGAAGGCGGCTTC[A/G]GAGTTGCAGAGCTCA | 105670 |
| rs582405377 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73161852 | TTCAGGCCAGGTTAA[C/T]GACTCTGGAGAAACA | 105670 |
| rs582494533 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73155627 | GCAGTATCCAGTGAT[A/G]CTGTTTCCCACCCAG | 105670 |
| rs582592171 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73175226 | ACACAGCCCTGCAGA[C/T]AGCCCTGCAGACAGC | 105670 |
| rs582634067 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73165593 | CACACACATACACAC[A/G]CACACACACACACAC | 105670 |
| rs582702699 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73150572 | AAATAAATAAATAAA[C/T]AAATAAATAAACAAA | 105670 |
| rs582791000 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73155362 | ATCCAGTGATGCTGT[C/T]TCCCATGCAGTATCC | 105670 |
| rs582833562 | snp | A/C | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73175194 | AGTCCTGAACACAGC[A/C]CTGCAGATAGCTCTG | 105670 |
| rs582904701 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73158850 | TGTCCCAGATATGAA[A/G]GTAGAAGGTGGCATA | 105670 |
| rs582952238 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73169151 | CCCCTCCCCATCCAC[C/T]CTCTGACTGCTCCAC | 105670 |
| rs582984497 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73151753 | GCCATCATTTACAAG[A/G]TTCTCGCTCGAAGAC | 105670 |
| rs583007185 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73175258 | CTGAACACAGCCCTG[C/T]AGATAGCCCTGCAGA | 105670 |
| rs583007725 | snp | A/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73163205 | AGGGTTACAGGTTAC[A/T]GGTAGCTGGAGTGGA | 105670 |
| rs583009449 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73159936 | CTGAGTCCACACCTT[A/G]TGGGCTGAGTTAACT | 105670 |
| rs583074126 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | GRCm38.p3 | 14:73141310 | TTTTGTTTGTTTCTT[C/T]GTTTTGGATTTTTGA | 105670 |
| rs583179289 | snp | G/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73146374 | CTTTCCTACGCACTG[G/T]GTGGCACTTCCCTTG | 105670 |
| rs583179891 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73172065 | GGCTTATACAGACTA[C/T]TTTTGCCTCAGAGCT | 105670 |
| rs583191661 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73179503 | CCATGGGCCTGGCTG[C/T]CCCCAGCACCCCAGG | 105670 |
| rs583201443 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73156453 | TCCCCACCCTCCCTC[C/T]CTCCCCCCTCCCCTC | 105670 |
| rs583203477 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73173353 | CACTCTGTAGACCAG[A/G]CTGGCCTCGAACTCA | 105670 |
| rs583345564 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73155659 | ATCCAGTGATGCTGT[C/T]TCCCACCCAGTATCC | 105670 |
| rs583351490 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73181328 | CCACTCTGTCATGTA[C/T]ACTTTCTTATGCTGT | 105670 |
| rs583368830 | snp | G/T | | | downstream-variant-500B | Rcbtb2 | GRCm38.p3 | 14:73184339 | CTCTCCATAGATATG[G/T]AAGGAAGGATGGATG | 105670 |
| rs583423543 | snp | G/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73148529 | CTGCTATGGAGTATA[G/T]AAATAAGCTGTCATA | 105670 |
| rs583429967 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73164933 | TCTCTCTCTCTCTCT[C/T]TCTCTCCTTTTGTCA | 105670 |
| rs583538916 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73163713 | AAGTCTGCAGGTGGC[A/G]GACACTCTTCTGTTT | 105670 |
| rs583585195 | snp | G/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73146863 | CTCTCCCGGTAGAGC[G/T]GCCTCCTCTTCTCTC | 105670 |
| rs583733878 | snp | A/G | | | upstream-variant-2KB, intron-variant | Rcbtb2 | GRCm38.p3 | 14:73141362 | CCTGGCTGTCCTGGA[A/G]CTCACTTTGTAGACC | 105670 |
| rs583738161 | snp | G/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73167679 | AACGTTTTCCTTCAA[G/T]AACTAGAAGAAAGGA | 105670 |
| rs583839310 | snp | A/C | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73169119 | TTCATTTTTTATACT[A/C]CATATTCCATTCCCC | 105670 |
| rs583841354 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73153603 | ATGCATTAGTCTCCA[C/T]TTCCAGTTGAGAAAA | 105670 |
| rs583938572 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73159986 | TGAGTGAGTGGGGAA[A/G]CAGAAAGTGTGGTCC | 105670 |
| rs583995818 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152572 | AGGATACAGCTAAGA[C/T]CCTTTTTTTTTTTTT | 105670 |
| rs584047220 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73175313 | CAGCCCTGCAGATAG[C/T]CCTGAACACAGGTCT | 105670 |
| rs584098492 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73165579 | CTATCTTATCATCGC[A/G]CACACATACACACAC | 105670 |
| rs584210093 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | GRCm38.p3 | 14:73141553 | TATCACTTTAAATGG[C/T]TAACCAAAACATGCC | 105670 |
| rs584227082 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73160964 | TGGGCCCTCCCCCAC[C/T]GATCACTAATTGAGA | 105670 |
| rs584265483 | snp | C/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73175056 | GCAGACAGCCCTGAA[C/G]ACAGCCCTGCAGACA | 105670 |
| rs584299890 | snp | G/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73150335 | TTAAATACATAGGGG[G/T]GTGTGTGTCACACAC | 105670 |
| rs584402821 | snp | A/C | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73175086 | AGCCCTGAACACAGC[A/C]CTGCAGGCAGCCCTG | 105670 |
| rs584466272 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73157564 | CTCCTACATGTGATG[C/T]GCAGTAAATCTTTGT | 105670 |
| rs584491745 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73156480 | CCTCCCTCCCTCCCC[C/T]CTCCCCTCCCTCTCC | 105670 |
| rs584646738 | snp | G/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73160950 | CACCCACAGTGGGCT[G/T]GGCCCTCCCCCACTG | 105670 |
| rs584660922 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73169517 | TGGGTGAAAATAACT[A/G]CATCTGACTCTTTTA | 105670 |
| rs584752141 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73176390 | GTCAGCTGCTGGGCC[A/G]CCCACAGCAGCAGCA | 105670 |
| rs584822981 | snp | A/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | Rcbtb2 | GRCm38.p3 | 14:73142589 | AGTGCTCCTTAATGA[A/G]ATCCGTAAGTATTTG | 105670 |
| rs584824956 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73150564 | TATGCATTAAATAAA[C/T]AAATAAATAAATAAA | 105670 |
| rs584827046 | snp | C/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73174305 | GGATTCAGCATTTCT[C/G]GAATGCCCAGCGAGT | 105670 |
| rs584833885 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73177712 | AGAACAAAAGAAGAG[C/T]CACTGATTAAAGAGA | 105670 |
| rs584883916 | snp | C/G | | | upstream-variant-2KB, intron-variant | Rcbtb2 | GRCm38.p3 | 14:73141441 | TGAGATTAAAGGCGT[C/G]CGTGTGCCACCACCC | 105670 |
| rs584889358 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73175338 | AGGTCTGCAGACAGC[C/T]CTGAACACAGCCCTG | 105670 |
| rs585012570 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73169218 | GTAGATGCCCCCACC[C/T]CCCACCCCACCTGAC | 105670 |
| rs585016935 | snp | C/G/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73155477 | GATGCTGTTTCCCAC[C/G/T]CAGTATCCAGTGATA | 105670 |
| rs585076969 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73161635 | CAGATGTGGGTGACT[C/T]TCAGCAACACACAGC | 105670 |
| rs585163899 | snp | C/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73167118 | ATCTTCATGCCTCTT[C/G]GCATAAAGTAGTAAG | 105670 |
| rs585187535 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73169161 | TCCACCCTCTGACTG[C/T]TCCACATCCCACACC | 105670 |
| rs585248469 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73155447 | AGTGATGCTGTCTCC[C/T]ACCCAGTATCCAGTG | 105670 |
| rs585327848 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73175233 | CCTGCAGATAGCCCT[A/G]CAGACAGCCCTGAAC | 105670 |
| rs585375631 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73165589 | ATCGCACACACATAC[A/G]CACACACACACACAC | 105670 |
| rs585450114 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152153 | ATGCAGGTGACAGAG[A/G]CAGCTATAACCCCCC | 105670 |
| rs585503150 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73145328 | CATGAAGTGTGTGGT[C/T]CCCTTGAGGTCTTTC | 105670 |
| rs585524374 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73155530 | TGATACTGTTTCCCA[C/T]GCAGTATCCAGTGAT | 105670 |
| rs585805708 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73165616 | ACACACACACACACA[C/T]ACAAAATGGAACTTA | 105670 |
| rs585810771 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73150580 | AAATAAATAAATAAA[C/T]AAACAAACAAATGAT | 105670 |
| rs585823669 | snp | A/G | | | upstream-variant-2KB | Rcbtb2 | GRCm38.p3 | 14:73138005 | TATGCATGGGAATGT[A/G]TAAATGTATTCATTC | 105670 |
| rs585881295 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73146389 | GGTGGCACTTCCCTT[A/G]ACAGTGCGCTGGCTT | 105670 |
| rs585889462 | snp | G/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73179630 | CTGACCTCTGAGCTA[G/T]ATCCCCAGCTGTCTT | 105670 |
| rs585983459 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73146357 | CCACCATCAGTGCAC[C/T]CCTTTCCTACGCACT | 105670 |
| rs585992064 | snp | A/C | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73162702 | GCAAGACGATGCACA[A/C]AGCCCTTCTGTTCTC | 105670 |
| rs586042080 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73178904 | GTGCTGTGACATGCA[C/T]CATGGACAAGCTCCA | 105670 |
| rs586054444 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73155632 | ATCCAGTGATACTGT[C/T]TCCCACCCAGTATCC | 105670 |
| rs586111579 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73171972 | CCAGGACAACCAGGG[C/T]TACACAGAGAAACCC | 105670 |
| rs586223958 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73163238 | AGGAGATTTCCTATA[C/T]CCTGGGACTGCAAGG | 105670 |
| rs586230390 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73169152 | CCCTCCCCATCCACC[C/T]TCTGACTGCTCCACA | 105670 |
| rs586334471 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73155551 | ATCCAGTGATGCTGT[C/T]TCCCACCCAGTATCC | 105670 |
| rs586335878 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73170778 | CTCAACCAAACGAGA[C/T]GCTTTTAAAAGGTTT | 105670 |
| rs586464839 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73175202 | ACACAGCACTGCAGA[C/T]AGCTCTGAACACAGC | 105670 |
| rs586490444 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152746 | TCTTCCTAATCATTC[C/T]CTTCCCTGCCCTTCC | 105670 |
| rs586498342 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73167940 | TCTGTAGCAGTGATG[A/G]AACATTTCCCTGTTA | 105670 |
| rs586670713 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73155395 | TGATACTGTTTCCCA[C/T]GCAGTATCCAGTGAT | 105670 |
| rs586680128 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73155735 | CCAGTATCCAGTGAT[A/G]CTGTTTCCCATGCAG | 105670 |
| rs586771918 | snp | G/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | GRCm38.p3 | 14:73141312 | TTGTTTGTTTCTTCG[G/T]TTTGGATTTTTGAGA | 105670 |
| rs586789462 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73159940 | GTCCACACCTTGTGG[A/G]CTGAGTTAACTACTG | 105670 |
| rs586792442 | snp | C/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73175289 | CAGCCCTGAACACAG[C/G]CCTGCAGACAGCCCT | 105670 |
| rs586797604 | snp | A/C | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73175038 | AGCCCTGAACACAGC[A/C]CTGCAGACAGCCCTG | 105670 |
| rs586814349 | snp | A/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73155113 | GACTTCTTAAGGACG[A/T]TAAGTGTCTCTTCAC | 105670 |
| rs586838162 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73169134 | ACATATTCCATTCCC[C/T]GCCCCTCCCCATCCA | 105670 |
| rs586856699 | snp | G/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | GRCm38.p3 | 14:73141443 | AGATTAAAGGCGTGC[G/T]TGTGCCACCACCCCG | 105670 |
| rs586864567 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73160959 | TGGGCTGGGCCCTCC[C/T]CCACTGATCACTAAT | 105670 |
| rs587016558 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73165125 | TTGTTTTTTTTTTTG[A/G]CTTTCAGTCTACAGT | 105670 |
| rs587020696 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73149672 | TTGTGCCACGGGTTG[C/T]CAGTCTGTTGGTAGA | 105670 |
| rs587022354 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73172771 | ATGAGATTGCCCAAT[C/T]ATAGACGTGAAGAGA | 105670 |
| rs587024714 | snp | A/T | | | downstream-variant-500B | Rcbtb2 | GRCm38.p3 | 14:73184345 | ATAGATATGGAAGGA[A/T]GGATGGATGGATGGA | 105670 |
| rs587182553 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73160207 | AAACCTTGCACCGTT[C/T]CAGGAAAAAGACAAA | 105670 |
| rs587203243 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73156786 | GTGACAGCTTGCCAG[C/T]TTGCTGTGCTCTACA | 105670 |
| rs587207122 | snp | G/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73181617 | CTGCATTCATCTTCA[G/T]CATTTGCTAGAGTTT | 105670 |
| rs587234301 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73146885 | TCTTCTCTCTCCCTC[C/T]CCCTCCCCCTCCCCC | 105670 |
| rs587250598 | snp | C/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73163781 | CTGGTCAGATGACAG[C/G]GTAGCCTTGCTTGCT | 105670 |
| rs587495053 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73173506 | TCAATAGATCCTCAT[A/G]TTATAAATGCCACCA | 105670 |
| rs587495119 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73156460 | CCTCCCTCCCTCCCC[C/T]CTCCCCTCCCTCCCT | 105670 |
| rs587526152 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | GRCm38.p3 | 14:73141363 | CTGGCTGTCCTGGAG[C/T]TCACTTTGTAGACCA | 105670 |
| rs587527885 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73175315 | GCCCTGCAGATAGCC[C/T]TGAACACAGGTCTGC | 105670 |
| rs864278758 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | GRCm38.p3 | 14:73183233 | GAAGAAGTATCATCT[-/A]AAAAATAAACATTAT | 105670 |
| rs864278844 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | GRCm38.p3 | 14:73183296 | TAGATATCTGTGGGG[A/G]ATTGATAGTTTGCTA | 105670 |