SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3704347 | snp | C/T | 0.455 | 0.143091 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73168777 | TGAAAGCTTCTGGCT[C/T]CTTTGGATAGTCACG | 105670 |
rs4230464 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Rcbtb2 | Mm_Celera | 14:73178283 | AACG[A/G] | 105670 |
rs4230465 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Rcbtb2 | Mm_Celera | 14:73178295 | CTCAGCTGTCTTCCC[A/G]GGGTGCTGTGAAGGC | 105670 |
rs4230466 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Rcbtb2 | Mm_Celera | 14:73178298 | AGCTGTCTTCCCGGG[A/G]TGCTGTGAAGGCGGC | 105670 |
rs4230467 | snp | C/G | 0.21875 | 0.248039 | intron-variant | Rcbtb2 | Mm_Celera | 14:73178312 | GGTGCTGTGAAGGCG[C/G]CTTCAGAGTTGCAGA | 105670 |
rs4230468 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rcbtb2 | Mm_Celera | 14:73178319 | TGAAGGCGGCTTCAG[A/T]GTTGCAGAGCTCATT | 105670 |
rs4230469 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rcbtb2 | Mm_Celera | 14:73178321 | AAGGCGGCTTCAGAG[C/T]TGCAGAGCTCATTTT | 105670 |
rs4230470 | snp | C/G | 0.21875 | 0.248039 | intron-variant | Rcbtb2 | Mm_Celera | 14:73178326 | GGCTTCAGAGTTGCA[C/G]AGCTCATTTTGCCCG | 105670 |
rs4230472 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Rcbtb2 | Mm_Celera | 14:73178362 | TGGAAGCCCTTCACA[A/G]CCCTCTGAGCACTGC | 105670 |
rs4230473 | snp | C/G | 0.21875 | 0.248039 | intron-variant | Rcbtb2 | Mm_Celera | 14:73178377 | GCCCTCTGAGCACTG[C/G]ACCTCAATGGTCAGG | 105670 |
rs4230474 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Rcbtb2 | Mm_Celera | 14:73178393 | ACCTCAATGGTCAGG[C/T]GCTCAGAGCGCACCC | 105670 |
rs4230475 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rcbtb2 | Mm_Celera | 14:73178403 | TCAGGCGCTCAGAGC[A/G]CACCCACAATACATT | 105670 |
rs4230476 | snp | A/C | 0.21875 | 0.248039 | intron-variant | Rcbtb2 | Mm_Celera | 14:73178415 | AGCGCACCCACAATA[A/C]ATTCTCCTTTCCATC | 105670 |
rs4230477 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Rcbtb2 | Mm_Celera | 14:73178421 | CCCACAATACATTCT[C/T]CTTTCCATCAGGGTT | 105670 |
rs4230478 | snp | G/T | 0.21875 | 0.248039 | synonymous-codon, nc-transcript-variant, intron-variant | Rcbtb2 | Mm_Celera | 14:73178524 | CTGTGAGGAGAATGC[G/T]ATTGCTCTGCTCTCT | 105670 |
rs4230479 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Rcbtb2 | Mm_Celera | 14:73178604 | CACTAAAAGTAACGT[A/G]TAGCTAGATGAAAAT | 105670 |
rs4230480 | snp | C/G | 0.21875 | 0.248039 | intron-variant | Rcbtb2 | Mm_Celera | 14:73178608 | AAAAGTAACGTGTAG[C/G]TAGATGAAAATGGAA | 105670 |
rs4230481 | snp | C/G | 0.21875 | 0.248039 | intron-variant | Rcbtb2 | Mm_Celera | 14:73178630 | AAAATGGAACATACA[C/G]AAATAAAGTCTTAGA | 105670 |
rs4230482 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Rcbtb2 | Mm_Celera | 14:73178633 | ATGGAACATACAGAA[A/G]TAAAGTCTTAGAGAA | 105670 |
rs4230483 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rcbtb2 | Mm_Celera | 14:73178641 | TACAGAAATAAAGTC[C/T]TAGAGAACTTATGTG | 105670 |
rs6179146 | snp | A/T | 0.5 | 0 | intron-variant | Rcbtb2 | Mm_Celera | 14:73158241 | GGGCCTTTGTTCTCC[A/T]GCACCTTGAAGGTTC | 105670 |
rs6179622 | snp | C/T | 0.5 | 0 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73158313 | AATATATAAAAACCA[C/T]AGAAGGCCACTAATA | 105670 |
rs6192749 | snp | G/T | 0.5 | 0 | intron-variant | Rcbtb2 | Mm_Celera | 14:73158449 | TGATATGAGGAGGTA[G/T]GTACTTTAAAATAGA | 105670 |
rs6193340 | snp | A/G | 0.5 | 0 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73158582 | TTTATGTTAAAACTC[A/G]TTGATTTCCAAGTTA | 105670 |
rs6193815 | snp | C/T | 0.5 | 0 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73158676 | CACATCACTGCAGCT[C/T]CTTGTACATGTGAGA | 105670 |
rs6194340 | snp | A/G | 0.5 | 0 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73158776 | GCTCTGGTGTTTAGT[A/G]ACTGAAGAAACAGTA | 105670 |
rs6301068 | snp | A/G | 0.5 | 0 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73164605 | TGGTGGATTCCATCG[A/G]TGGCAATCCAGGCAC | 105670 |
rs6301134 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73164657 | AAGCACAGGCCGTGA[C/T]GGCTGCTTACCTTCT | 105670 |
rs6301238 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73138058 | ATGTATGAAGGCAAC[A/G]NTAAGCCCCGGGGAC | 105670 |
rs6301240 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73138059 | TGTATGAAGGCAACN[G/T]TAAGCCCCGGGGACC | 105670 |
rs6301795 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73138136 | ctgatcctggagttg[A/G]ctctttggctagact | 105670 |
rs6302667 | snp | C/T | 0.5 | 0 | intron-variant | Rcbtb2 | Mm_Celera | 14:73164901 | tctctctttctctct[C/T]tctctctctctctct | 105670 |
rs6302862 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73138343 | aaaggcatgtaccac[C/T]atgcctggcAAAAAG | 105670 |
rs6302926 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73138389 | AGCTATGTATTGGGG[A/G]AAACATTATAAGTAA | 105670 |
rs13470926 | snp | C/T | 0.444444 | 0.157135 | utr-variant-5-prime, nc-transcript-variant | Rcbtb2 | GRCm38.p3 | 14:73154325 | TCCAGCTTAGCAGAT[C/T]ATACATTCTTCAGGA | 105670 |
rs30153117 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Rcbtb2 | Mm_Celera | 14:73174128 | TGTCTTTCAGATAAA[A/T]AATATATCTAGAAAC | 105670 |
rs30170712 | snp | A/G | 0.5 | 0 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73182448 | CATCAAGCTGTTGTT[A/G]TTGTTCCTAGGACTT | 105670 |
rs30275061 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73183662 | CTTCTCATAATGGCA[C/T]TGTTGAAAATAAAAC | 105670 |
rs30356833 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73170246 | TTCCACTGGCTCACT[C/T]TGGAGCAGACTGTGG | 105670 |
rs30360364 | snp | C/T | 0.5 | 0 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73145902 | AATGTACATTGTTCT[C/T]CCCACCCCCAGTACA | 105670 |
rs30362417 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Rcbtb2 | Mm_Celera | 14:73174130 | TCTTTCAGATAAAAA[A/T]TATATCTAGAAACAG | 105670 |
rs30385757 | snp | A/C/G | 0.444444 | 0.157135 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73145749 | TTATCTGGAAGAAGC[A/C/G]TGTGTCTCTTTCAGG | 105670 |
rs30414891 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73153877 | ACAGGGTTTCTCTGT[A/G]TAGCCCTGGCTGTCC | 105670 |
rs30433102 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rcbtb2 | Mm_Celera | 14:73182325 | CATGGACTAATTGTT[A/G]ATAATTGCTGTAGCT | 105670 |
rs30447124 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Rcbtb2 | GRCm38.p3 | 14:73137733 | CTCTGCCACTCTCCA[C/T]GCCCTCTGGGAACTG | 105670 |
rs30474300 | snp | A/G | 0.5 | 0 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73144257 | GGCGATTAAAGCCGA[A/G]TAAAAGAGACCGAGT | 105670 |
rs30476818 | snp | A/C | 0.5 | 0 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73151688 | TACACAGGAAGACTG[A/C]CCCAGCAGTAGGAGC | 105670 |
rs30486899 | snp | C/T | 0.432133 | 0.171253 | upstream-variant-2KB | Rcbtb2 | GRCm38.p3 | 14:73138004 | GTATGCATGGGAATG[C/T]GTAAATGTATTCATT | 105670 |
rs30504971 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73148375 | AAGGTCTTCCTTCCT[C/T]ATCTTGGTTTGTATC | 105670 |
rs30509175 | snp | C/G | 0.444444 | 0.157135 | intron-variant, utr-variant-5-prime | Rcbtb2 | Mm_Celera | 14:73143368 | TGGACCAGGTCGCTG[C/G]GGTAGCTCTGGGTTC | 105670 |
rs30509830 | snp | A/G | 0.5 | 0 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73150006 | TTACAGCACAGTCTC[A/G]GGCCTCTTGCTTTTG | 105670 |
rs30522443 | snp | A/G | 0.32 | 0.24 | intron-variant | Rcbtb2 | Mm_Celera | 14:73149023 | TAGAGTCACAATGGC[A/G]GTGCTCTTGTTTTAG | 105670 |
rs30586648 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rcbtb2 | Mm_Celera | 14:73150181 | GGGACCTGGGTTCAA[G/T]TCCCAGCACCCACAT | 105670 |
rs30728361 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rcbtb2 | Mm_Celera | 14:73180419 | AAAATCCTTAAATAC[A/G]CTGAAGCTCTAGTGA | 105670 |
rs30736436 | snp | A/G | 0.5 | 0 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73160294 | AATGGGATTGGGCCT[A/G]GTATTCCTTGTTTTA | 105670 |
rs30750155 | snp | A/G | 0.5 | 0 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73177784 | ATGTATGTCCCCACA[A/G]TACACTCTGGGTGAG | 105670 |
rs30766073 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | GRCm38.p3 | 14:73183401 | AGCCTCTAACATAGT[A/G]CCTTATATATAAAAG | 105670 |
rs30790956 | snp | C/T | 0.444444 | 0.157135 | intron-variant, utr-variant-5-prime | Rcbtb2 | GRCm38.p3 | 14:73143795 | CGCCTGAGTTGAAGC[C/T]AGGCTTCCAGCCGCC | 105670 |
rs30807742 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73169452 | TCTCCTCAGCTTCTT[A/T]CAGTTTTTCCTAATT | 105670 |
rs30837879 | snp | C/G | 0.465374 | 0.126941 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73170017 | GGATGGCTTAAGACT[C/G]TAACTATAACAACGC | 105670 |
rs30847105 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73143890 | CTCCCTTGCACACCC[A/T]GAGATTGCCCTGGCT | 105670 |
rs30871176 | snp | C/T | 0.5 | 0 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73145879 | GCTCTACTCATCTAA[C/T]CTGAGCTAATGTACA | 105670 |
rs30906434 | snp | C/G | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Rcbtb2 | GRCm38.p3 | 14:73141946 | TCAGCCTCAGGAACC[C/G]TGAACTTGCTCAAGA | 105670 |
rs30917774 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Rcbtb2 | Mm_Celera | 14:73174129 | GTCTTTCAGATAAAA[A/T]ATATATCTAGAAACA | 105670 |
rs30922497 | snp | A/C/T | 0.48 | 0.0979796 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73180250 | AGTGAGCCAGTCTGA[A/C/T]GTGTAGAGAGAAGTG | 105670 |
rs30965758 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rcbtb2 | Mm_Celera | 14:73153528 | TAAGCAGGCCTTTAA[A/C]ACTGACTTTTCAAAC | 105670 |
rs30970800 | snp | A/G | 0.5 | 0 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73151414 | GCTATTTTTTAATAC[A/G]AGACATGATACAATT | 105670 |
rs30973189 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73148487 | AGAGCGTACTATGGA[C/G]TATGTAAATAAGCCA | 105670 |
rs30993846 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73146091 | ATAGTTACCTCATCT[A/G]TTAATACCTATTTAA | 105670 |
rs30995700 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rcbtb2 | Mm_Celera | 14:73175739 | TTCTTTCCTGCCTGC[C/T]TCTTTCCTTCCTAAC | 105670 |
rs31012249 | snp | G/T | 0.465374 | 0.126941 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73170340 | TAGCTTCCGGGCTCT[G/T]AGCATCCTGCCCAGC | 105670 |
rs31015215 | snp | A/G | 0.5 | 0 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73150112 | CCAAAGATAAGATAT[A/G]TCCTATGGCTGGCAA | 105670 |
rs31058640 | snp | A/C | 0.5 | 0 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73144387 | CTGTCACCGTATTGG[A/C]CAATGGCATGCAGGT | 105670 |
rs31210806 | snp | C/T | 0.5 | 0 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73154815 | CTTCTGATTTTACCA[C/T]GTACTTTTTCCTCAG | 105670 |
rs31222259 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73147991 | ACAACTCCTTAGTAA[C/T]GATTATTTCACTAAC | 105670 |
rs31231837 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Rcbtb2 | Mm_Celera | 14:73174132 | TTTCAGATAAAAAAT[A/T]TATCTAGAAACAGTC | 105670 |
rs31245062 | snp | A/G | 0.5 | 0 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73173412 | GCTGGGATTAAAGGC[A/G]TGCGCCACCACGCCC | 105670 |
rs31277074 | snp | C/T | 0.5 | 0 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152339 | ACATTAGTAATTTGT[C/T]TTGAGTTATTTTTAA | 105670 |
rs31284098 | snp | A/G | 0.5 | 0 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73153924 | GACCAGGCTGGCCTC[A/G]AACTCAGAAATCTGC | 105670 |
rs31306286 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73153245 | AGTGCCATTCTTGAG[C/G]TTGCAAAGAGAGAAG | 105670 |
rs31334663 | snp | A/G | 0.5 | 0 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73153357 | AGTGCCATAATATAT[A/G]ATGGTGATTAACTAT | 105670 |
rs31338331 | snp | C/T | 0.5 | 0 | intron-variant | Rcbtb2 | Mm_Celera | 14:73179647 | TCCCCAGCTGTCTTG[C/T]TTATTTTGAGGCAGA | 105670 |
rs31339516 | snp | A/G | 0.5 | 0 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73144252 | GTTTTGGCGATTAAA[A/G]CCGAGTAAAAGAGAC | 105670 |
rs31371706 | snp | C/T | 0.444444 | 0.157135 | intron-variant, utr-variant-5-prime | Rcbtb2 | GRCm38.p3 | 14:73143441 | CGCGCAGGCCCAGCC[C/T]GGGGTCCGTTTTGTG | 105670 |
rs31387374 | snp | A/G | 0.32 | 0.24 | intron-variant | Rcbtb2 | Mm_Celera | 14:73181167 | AGTGGTAGTTTCTTA[A/G]GAACATTTGGTTTCC | 105670 |
rs31460023 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rcbtb2 | Mm_Celera | 14:73159755 | CCTCCCCTCGTCCCC[A/G]CCACCCCTCCCCCAG | 105670 |
rs31474068 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Rcbtb2 | Mm_Celera | 14:73149258 | TCATCAAAAGATTTT[C/G]TGTGAGAATTCTCGT | 105670 |
rs31511732 | snp | A/G | 0.5 | 0 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73144198 | AACGGAGAGGCGAAC[A/G]TGTTTCTCTTTAGAA | 105670 |
rs31529205 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73148725 | AGTTGTCCCAATATG[A/G]ATATCCACGTCTGCT | 105670 |
rs45679238 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73153127 | GTATATGTGTCATAT[A/G]TCCTGGTAGCTCTAG | 105670 |
rs45692261 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rcbtb2 | Mm_Celera | 14:73181302 | TTCTGTAGAACTCAA[C/T]CTAAGCGGTGCCACT | 105670 |
rs45761833 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73162162 | AAATTGAAGACATCC[A/G]GGGAAACTAAGGAAT | 105670 |
rs45779713 | snp | C/T | 0.32 | 0.24 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73179401 | GGAGTGCCCTTTTCC[C/T]TTTTGGTAAACAGTA | 105670 |
rs45791814 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73157781 | TGAAAAGCAATAATA[C/T]ACTCCTATGTCTAGT | 105670 |
rs45834008 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73144802 | GAATTTGGGGGAGGG[A/G]GATTATTATTAACAA | 105670 |
rs45865716 | snp | A/C | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73166473 | ATCAGTCTTTTCTTT[A/C]CCATAGGTGTTTGCC | 105670 |
rs45896650 | snp | A/C | 0.32 | 0.24 | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137303 | GGCTGCTGTAGTTCT[A/C]CTGAGGTCAAGGCCA | 105670 |
rs45923073 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73157649 | ATTAAATATTGTCTC[C/T]AAATAGTATATGCAT | 105670 |
rs45956782 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73165669 | TACAACAAAGACTGT[C/T]TACCAATGAAAGGTC | 105670 |
rs45979166 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rcbtb2 | Mm_Celera | 14:73164180 | AGCACACATGTGATT[C/G]ATTCATTCAAAGTGC | 105670 |
rs46014391 | snp | A/C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73155030 | TAATAGTATAGGGAC[A/C/T]TAGGATGTGGATGGG | 105670 |
rs46018889 | snp | A/G | 0.124444 | 0.216185 | utr-variant-5-prime | Rcbtb2 | Mm_Celera | 14:73138806 | TGTCAAGAATGTCCC[A/G]GTGTGATCAACTCAG | 105670 |
rs46042571 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152888 | TTCTAGTAAATTTGA[C/T]GTTAAATATGAAAAA | 105670 |
rs46077421 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73164316 | TCCATAAAATTGCAC[A/G]TTTTATGAATTTTTA | 105670 |
rs46138468 | snp | A/C | 0.18 | 0.24 | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73183432 | GCACTCAGTTAATTC[A/C]CTGTCCATCATAAGG | 105670 |
rs46145179 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73157679 | TTTATAAATTAAGCT[A/G]TCAGTCTGCTATGTA | 105670 |
rs46173421 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137117 | GCTGTTAGAGAGAAG[C/T]CCCTGGAAGGCTTGT | 105670 |
rs46188684 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159262 | GTAATGAACTTAGTT[A/G]AGATGAGGTCATAAA | 105670 |
rs46190369 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137018 | GCAGTCCTCTCTAGA[C/T]TCACATTGGCTCAAG | 105670 |
rs46241763 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Rcbtb2 | Mm_Celera | 14:73171327 | CCACTTACCTGTCAC[A/C]TCAGCTCAACACTGC | 105670 |
rs46302704 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73155492 | TCAGTATCCAGTGAT[A/G]CTGTTTCCCACGCAG | 105670 |
rs46312908 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73157498 | ACCTGACAGCGGAAG[A/G]CTAAAATGTAGGCAT | 105670 |
rs46386921 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73165878 | GAGGCTGTGGTCCAG[A/G]TCAAAGGTAAATCTT | 105670 |
rs46394470 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Rcbtb2 | Mm_Celera | 14:73140460 | GGCCCAAAGTGAGAA[A/T]AGTTCAGGTGGTGTT | 105670 |
rs46458200 | snp | A/G | 0.32 | 0.24 | intron-variant | Rcbtb2 | Mm_Celera | 14:73179096 | AATGAACCAAAGAAC[A/G]AATGGCAAACATAAT | 105670 |
rs46472235 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159368 | GCCGGCAGTACAGAC[A/C]GACAAAGGGAAGAAA | 105670 |
rs46485308 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73164216 | CAGAAAAGGAAGTCA[C/T]TTTGTGGAAGGTGCG | 105670 |
rs46487099 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73160689 | TCAGTTTGGGTTTCA[A/G]TTGCTGCAGCCAAGC | 105670 |
rs46548085 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73161251 | ATGGGGATTCATGGC[C/T]CATCAGTCAGTTTTC | 105670 |
rs46565965 | snp | G/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73163219 | CAGGTAGCTGGAGTG[G/T]AATAGGAGATTTCCT | 105670 |
rs46580277 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73154724 | CCGGTGTCTCTAATT[C/T]CTTAGCCTTCCAAAT | 105670 |
rs46589160 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152975 | AGGCCTGGGATTGTT[A/G]CTCAGTGGTAGCAAT | 105670 |
rs46596390 | snp | A/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73165932 | AAGGTGGACCTTCTC[A/T]CTTCAAATGATTTAA | 105670 |
rs46677735 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73167537 | TATATATGCTACCAC[A/T]TAAAAATGTCTAAGT | 105670 |
rs46697165 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137656 | TCTCAAAGCTATTAT[C/T]TGGGGTTCGCCTGGA | 105670 |
rs46706049 | snp | G/T | 0.391111 | 0.206368 | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73136880 | ATTAGTCCCATGGCT[G/T]CTTTAGTGACTTGGG | 105670 |
rs46744475 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rcbtb2 | Mm_Celera | 14:73171638 | CTCCAGGTGGAAGCC[A/G]AGCTCCCAGTCTGGC | 105670 |
rs46767380 | snp | A/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152981 | GGGATTGTTACTCAG[A/T]GGTAGCAATGCTTGC | 105670 |
rs46797833 | snp | A/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152965 | TTAAGTGCTTAGGCC[A/T]GGGATTGTTACTCAG | 105670 |
rs46813692 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rcbtb2 | Mm_Celera | 14:73172550 | GGGATCAGGATTAGT[A/C]CACTAGCCACACTTC | 105670 |
rs46853271 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rcbtb2 | Mm_Celera | 14:73171303 | CACCTCCTTGTCCAG[A/G]GCTCTCTCCCACTTA | 105670 |
rs46886628 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152027 | GATTGTGCCTTCTTT[C/T]TATGATTATGGTCTG | 105670 |
rs46932767 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rcbtb2 | Mm_Celera | 14:73166927 | GAGTGTCCTCATGCA[C/T]GTTCAGCTGCTGGGA | 105670 |
rs46953029 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rcbtb2 | Mm_Celera | 14:73172595 | TGAAATCGCGTGACA[C/T]TGAAGTTCCCTGTTT | 105670 |
rs47099593 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73163734 | TCTTCTGTTTGGGAA[C/T]GTGGCTCCTGCTCTT | 105670 |
rs47153670 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73136954 | ATGCTCTTGTGCCTG[A/G]CTCGGAGGGTCTCCA | 105670 |
rs47184254 | snp | A/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73156912 | TCTGGTAGTATGTTT[A/T]CCTTGTCATAGTTAA | 105670 |
rs47302432 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rcbtb2 | Mm_Celera | 14:73172243 | ACCAGATCGTTTGGG[C/T]CATTTTCTCATTGTG | 105670 |
rs47324140 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73159598 | TTGAATGTCAACTTG[C/T]CACAAAGTAGAATCA | 105670 |
rs47385375 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152095 | CAGCGTTCCACACAC[C/T]AGGCTTATGTTTTAC | 105670 |
rs47453791 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73151023 | CAGCTTGGGCTATAC[A/G]AAAGGACCCTGTCTC | 105670 |
rs47453803 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Rcbtb2 | Mm_Celera | 14:73180482 | CTACATTGTTGCAGT[A/C]GAGCCCTGCGGAAAG | 105670 |
rs47477753 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rcbtb2 | Mm_Celera | 14:73168863 | TTCCCCTATAAGCCA[A/G]TGATGCTGTCGCTCT | 105670 |
rs47494486 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73166469 | GTTTATCAGTCTTTT[C/T]TTTCCCATAGGTGTT | 105670 |
rs47495016 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73168296 | CCAGGCAGTGGCTCA[C/T]GCCTTTAATCCTAGT | 105670 |
rs47497860 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73154636 | ACCCGCTCACCATAT[C/T]GGGACTTCTTTTCCC | 105670 |
rs47541737 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165171 | GTCAGGGAAGAAACT[C/G]AAGACAGGAACCTAG | 105670 |
rs47571260 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73147242 | TAGCCTCAGGGCCCA[C/T]AGTTTGATCAGACAT | 105670 |
rs47576765 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rcbtb2 | Mm_Celera | 14:73164645 | TGTCCTATAGAGAAG[C/T]ACAGGCCGTGACGGC | 105670 |
rs47615765 | snp | A/G | 0.32 | 0.24 | intron-variant | Rcbtb2 | Mm_Celera | 14:73172060 | GATATGGCTTATACA[A/G]ACTACTTTTGCCTCA | 105670 |
rs47617236 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rcbtb2 | Mm_Celera | 14:73172734 | ACACCCTTCTTTGGC[C/T]TAGCCCACTTCATCT | 105670 |
rs47651247 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rcbtb2 | Mm_Celera | 14:73172092 | AGCTAGTGTTGTGCC[C/T]AAACCAGGATGCTCT | 105670 |
rs47680654 | snp | G/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73163808 | TGCTCATGTGGAAAA[G/T]GAGCATGCGTGAGCA | 105670 |
rs47698339 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152809 | AACCCGGAACCTCAC[C/T]CATCTGCTCTCATTG | 105670 |
rs47705194 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73138440 | CTTGGAATCATACTT[C/T]TACAACTTTATAGAA | 105670 |
rs47712689 | snp | A/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73166139 | TTCTTGGTAGCAATT[A/T]ATTGCCATGGTGGTT | 105670 |
rs47718266 | snp | C/T | 0.32 | 0.24 | intron-variant | Rcbtb2 | Mm_Celera | 14:73172185 | CTAGTAGATGGATTT[C/T]ATTGGCTGTTTCCAT | 105670 |
rs47745060 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73155384 | GCAGTATCCAGTGAT[A/G]CTGTTTCCCACGCAG | 105670 |
rs47767938 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73167697 | CTAGAAGAAAGGATT[A/T]ATGCGTCTGTCTTAC | 105670 |
rs47822648 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Rcbtb2 | Mm_Celera | 14:73176429 | CAATGTAGAGTCAGA[A/T]GCCTGGGCCACCTGC | 105670 |
rs47865655 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73161089 | GTCCAGCCTAGCCCA[C/T]AAAGGGCAGTGCAAG | 105670 |
rs47866272 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73164419 | TTAAGGAACACCTCG[A/C]ACTTTGATTTTCGCT | 105670 |
rs47874407 | snp | A/G | 0.32 | 0.24 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73153280 | TTGGGTGAGTCAGGA[A/G]GCACAGCGGTAATGG | 105670 |
rs47972245 | snp | G/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73140493 | CCCAGAGATCTGGGG[G/T]CCCAATCCTGCTGGT | 105670 |
rs48031947 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rcbtb2 | Mm_Celera | 14:73167825 | GCAGCGCTGGCCATT[C/T]GGCTGGGTCTGTGCT | 105670 |
rs48035900 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73157492 | TCCCTCACCTGACAG[C/T]GGAAGACTAAAATGT | 105670 |
rs48089092 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73157646 | ACTATTAAATATTGT[C/T]TCCAAATAGTATATG | 105670 |
rs48109861 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73163807 | TTGCTCATGTGGAAA[A/G]GGAGCATGCGTGAGC | 105670 |
rs48112731 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rcbtb2 | Mm_Celera | 14:73153311 | TTACAGTAGGGTTTA[A/C]AGAAAATGAGGATTC | 105670 |
rs48145686 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73157775 | CAGATTTGAAAAGCA[A/G]TAATATACTCCTATG | 105670 |
rs48163455 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73163320 | TTCCTTGGTGAATTC[C/T]AGGAAGGAAAAGGAG | 105670 |
rs48187804 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Rcbtb2 | Mm_Celera | 14:73140093 | GTGATGATCCTTTGA[C/T]GTGTTTCCATGCCAG | 105670 |
rs48254884 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73145112 | TATAGACTTGCTGGG[A/G]TTTGGGTCCTGCAGC | 105670 |
rs48266088 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73154593 | TTAGAGCTGTTGCCT[C/T]CCATGCTAAAGGCTT | 105670 |
rs48286045 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152989 | TACTCAGTGGTAGCA[A/G]TGCTTGCTCTGCATG | 105670 |
rs48289676 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73166164 | GTGGTTTTATTATGA[C/T]GTTTCCTTGTATGTA | 105670 |
rs48394071 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73166307 | TGAGGTGGAGAGGTA[A/G]TTTTGTGTCATATGA | 105670 |
rs48453582 | snp | C/T | 0.32 | 0.24 | intron-variant | Rcbtb2 | Mm_Celera | 14:73172251 | GTTTGGGCCATTTTC[C/T]CATTGTGCAGGGCCA | 105670 |
rs48458661 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73164374 | TAAAATGTGGTCATC[A/G]TCTCTAAAGGAAGTG | 105670 |
rs48564891 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73162701 | TGCAAGACGATGCAC[A/G]AAGCCCTTCTGTTCT | 105670 |
rs48588815 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73166120 | TCCCTCAAATTCAGC[C/T]TTATTCTTGGTAGCA | 105670 |
rs48609685 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73164238 | GAAGGTGCGCATATC[G/T]AGGGCTTTGGGGAAA | 105670 |
rs48614629 | snp | A/C/G | 0.489796 | 0.070696 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73167399 | TTATACTTGGGTTCC[A/C/G]CAGCCTTCTAACTAC | 105670 |
rs48662291 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73167842 | GCTGGGTCTGTGCTC[A/G]TTCGAAGAGTACTTG | 105670 |
rs48670587 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73151105 | TTATATTTCATGGGG[A/C]TTCTTTTTTGTTGAT | 105670 |
rs48740466 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73164189 | GTGATTGATTCATTC[A/T]AAGTGCAGAATCAGA | 105670 |
rs48741060 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rcbtb2 | Mm_Celera | 14:73172361 | AACCCAAGTGCATGA[C/T]CCAAATACAATCTTG | 105670 |
rs48741663 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73163630 | TTAGAGTCGGCCAGT[A/G]CTTCTCTCCATTAAG | 105670 |
rs48745927 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73155368 | TGATGCTGTTTCCCA[C/T]GCAGTATCCAGTGAT | 105670 |
rs48859814 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137490 | CTGACCTGGCAGTGG[A/G]CAGAGAAAAGCTTGT | 105670 |
rs48867132 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73158495 | CTCACAACACAGGTC[C/T]GTTATCTGTGAACCA | 105670 |
rs48897974 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rcbtb2 | Mm_Celera | 14:73171199 | CTGAAGATGGGGCTT[A/G]GCTGAAGCAGTGTCC | 105670 |
rs48905288 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73155424 | ATACTGTTTCCCACC[C/T]AGTATCCAGTGATGC | 105670 |
rs48923900 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73167140 | AGTAGTAAGTCTACT[C/T]TTAGAGAATTGTCCT | 105670 |
rs48931570 | snp | A/T | 0.231111 | 0.249285 | downstream-variant-500B | Rcbtb2 | Mm_Celera | 14:73184261 | TATTGGTAAAATTAC[A/T]GTATTAAGAGTTCTC | 105670 |
rs48974075 | snp | A/C | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant, intron-variant | Rcbtb2 | Mm_Celera | 14:73164760 | TCATGGTTTAGTGCC[A/C]TGCCATATCTCTACG | 105670 |
rs49013136 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73167028 | TATGGTCCTGGTGTG[A/T]GCTGTCCTGGAAATG | 105670 |
rs49101900 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73175980 | GCCTACACCATGACA[A/G]CGCACTTTATCATAT | 105670 |
rs49117398 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137627 | CCTGCTTGATCAGTA[C/T]TCTGTCTTTTCTGTC | 105670 |
rs49194207 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159186 | CCCCCAAGACTATGA[G/T]CCAAAGTCCAATACC | 105670 |
rs49205001 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rcbtb2 | Mm_Celera | 14:73172543 | AACCTCAGGGATCAG[A/G]ATTAGTCCACTAGCC | 105670 |
rs49233338 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73145636 | GTCCAAGGCTGAAAA[C/T]AAGTGGGAATGCCCC | 105670 |
rs49294548 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152943 | GCAAGAGAGGGGAAG[A/G]GCACCCTTAAGTGCT | 105670 |
rs49294948 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73157227 | AGACATTCACATCAC[A/G]GAGCATCACTCCTCA | 105670 |
rs49375651 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rcbtb2 | Mm_Celera | 14:73171262 | TCTGTCATGCACATT[A/G]TCCTTAGAACACTGT | 105670 |
rs49402713 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159452 | TTAGGGGCAAGCTAG[A/C]TGACACCTGGACTTG | 105670 |
rs49474405 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159304 | ATCCAGTCTGACTTG[A/G]GTGTTTCTCAGAAAG | 105670 |
rs49524258 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73136791 | CTCCCTTTGAGATGT[A/G]CCTGCGATCATCAGT | 105670 |
rs49533787 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73138495 | CCAACATCTCATCAT[C/T]GAGAGAACTGCTCGA | 105670 |
rs49558175 | snp | C/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73163340 | AGGAAAAGGAGAAGA[C/G]TGAGTAAAACCATCC | 105670 |
rs49602673 | snp | G/T | 0.489796 | 0.070696 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73167799 | CAGCTGAAGAACTGG[G/T]GTTGCTATCTGCAGC | 105670 |
rs49605824 | snp | A/G | 0.336735 | 0.234472 | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137279 | TGTCTTATGGCCCAG[A/G]GATCGCTGGGCTGCT | 105670 |
rs49635146 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73164028 | TGGAAAAGACCCAGT[A/G]AACAATTATTGTCAA | 105670 |
rs49648018 | snp | G/T | 0.244898 | 0.249948 | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137376 | ATCAGGTGAACGGGT[G/T]GATTTATCTAACTAA | 105670 |
rs49696212 | snp | A/G | 0.42 | 0.183303 | intron-variant | Rcbtb2 | Mm_Celera | 14:73180255 | GCCAGTCTGAAGTGT[A/G]GAGAGAAGTGTCCTG | 105670 |
rs49703969 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rcbtb2 | Mm_Celera | 14:73166213 | ACAAATCTTAAAAGG[A/G]CCCATTATTACTTTT | 105670 |
rs49765382 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73166394 | GCTCCCTGGGAGGGT[A/G]CTGAGGTGCCCTGAG | 105670 |
rs49781352 | snp | A/G | 0.124444 | 0.216185 | utr-variant-5-prime | Rcbtb2 | Mm_Celera | 14:73138909 | TTCCCAACATTTACT[A/G]AGTGCATGGATGTAG | 105670 |
rs49791310 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73157027 | CCAAAGGAAGTGATC[A/G]TGTAGTCAGGAGGGT | 105670 |
rs49792717 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73136855 | CTCGGCCCTGCAAAT[A/G]TGATGGGCCATTAGT | 105670 |
rs49795542 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73151181 | TACTCGGGGGCAGAG[C/T]AGGGGATCTAGAGTT | 105670 |
rs49796207 | snp | A/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73155222 | GAAGCTACGCTTCCA[A/T]CTCACTGTGCTCTTT | 105670 |
rs49815997 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169640 | CACCTTGAGCTGGAT[C/T]CCACTTTGGGCCTGT | 105670 |
rs49817778 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73166370 | GCCTGTACTGGGGAC[A/G]GTGAGGGAGCTCCCT | 105670 |
rs49857157 | snp | C/T | 0.32 | 0.24 | intron-variant | Rcbtb2 | Mm_Celera | 14:73170111 | GTCACATGGAGGCAG[C/T]AAGGACAGAAAGGTG | 105670 |
rs49901829 | snp | A/G | 0.391111 | 0.206368 | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137581 | GAGAGAACAAGAGGC[A/G]AAGGCTGGAGACGAA | 105670 |
rs49916694 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rcbtb2 | Mm_Celera | 14:73170799 | TAAAAGGTTTGGCAC[A/G]TGTGTCCTTAAGTTG | 105670 |
rs49954610 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73157962 | ATTGCATGAACCTCA[C/T]TCACACAGAGGAATC | 105670 |
rs49966055 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165105 | TTTTTTTTGTTTTTT[G/T]TTTTTTGTTTTTTTT | 105670 |
rs49989249 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73150682 | ACCCCTCTGTAAGTA[C/T]GCCACTGTCCCTAGG | 105670 |
rs50064405 | snp | C/G | 0.497041 | 0.0383476 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73163786 | CAGATGACAGCGTAG[C/G]CTTGCTTGCTCATGT | 105670 |
rs50076316 | snp | C/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152996 | TGGTAGCAATGCTTG[C/G]TCTGCATGTTCGAGA | 105670 |
rs50106553 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73146208 | ACATATTTTCCCACT[C/T]GACGGCCACGTTTTG | 105670 |
rs50109677 | snp | G/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73156789 | ACAGCTTGCCAGTTT[G/T]CTGTGCTCTACAGTG | 105670 |
rs50130456 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73166794 | TTACAATGGCAATGG[A/G]CAGCTGGGCCTGGGC | 105670 |
rs50143015 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73166708 | GTCACATAAGCATGG[C/T]GTGCTCCTCACAACA | 105670 |
rs50165535 | snp | A/G | 0.391111 | 0.206368 | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137419 | CAGATGACCTGTCTG[A/G]GAGTTTTGCCACATC | 105670 |
rs50188513 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73157210 | GGCGTTTATTTTTGC[A/G]TAGACATTCACATCA | 105670 |
rs50227320 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rcbtb2 | Mm_Celera | 14:73180491 | TGCAGTAGAGCCCTG[C/T]GGAAAGGCCTGAGAG | 105670 |
rs50231222 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73157311 | TACTGGCTTGCTACT[A/G]GCTTGCTTCTGACTT | 105670 |
rs50262258 | snp | A/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73145065 | TGCATGGCACATTGC[A/T]TCTTTTGTAAGTGAC | 105670 |
rs50345490 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Rcbtb2 | Mm_Celera | 14:73139510 | GAATAAGATGTTTCA[A/C]TATAACATGATGGTA | 105670 |
rs50377252 | snp | A/C | 0.32 | 0.24 | intron-variant | Rcbtb2 | Mm_Celera | 14:73164399 | GAAGTGAAGACCCAG[A/C]AGAGTTAAGGAACAC | 105670 |
rs50424184 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73176714 | CTTGGTGGGAACTGC[C/T]TACTGGAACCACCCT | 105670 |
rs50428263 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rcbtb2 | Mm_Celera | 14:73177516 | TGCCCCAGAGTAGAT[C/T]AAGGCCATGTCTGCT | 105670 |
rs50435167 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rcbtb2 | Mm_Celera | 14:73168582 | CTTCTATAGCTTGGG[A/G]AAACGATGGTACTTT | 105670 |
rs50446096 | snp | A/G | 0.244898 | 0.249948 | utr-variant-5-prime | Rcbtb2 | Mm_Celera | 14:73138863 | GCTGAATTACCATGT[A/G]AGTAGAAATCGGGGA | 105670 |
rs50510856 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159329 | AGAAAGGGAATTTTG[A/G]ACACAAAGATCCACA | 105670 |
rs50515699 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Rcbtb2 | Mm_Celera | 14:73170430 | CAAGTGTACTTGGTA[A/T]TGCAGGATGGATATT | 105670 |
rs50520507 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73176731 | ACTGGAACCACCCTA[C/G]TACTGTCACAAATCA | 105670 |
rs50612170 | snp | A/G | 0.5 | 0 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73167667 | TTTTCCACATTAAAC[A/G]TTTTCCTTCAAGAAC | 105670 |
rs50638376 | snp | A/C | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73163636 | TCGGCCAGTACTTCT[A/C]TCCATTAAGTGCCTG | 105670 |
rs50663431 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73150644 | TCAGAGTGCAGACTG[A/G]CTGAATCATTTGTGT | 105670 |
rs50672012 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152887 | ATTCTAGTAAATTTG[A/G]CGTTAAATATGAAAA | 105670 |
rs50753060 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73157125 | TCCTATATTTTCTTG[C/T]TCATGACTAGTTGTC | 105670 |
rs50756857 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73166902 | GGGCGGGGGGCGGTG[C/T]ACCAGAGCCGAGTGT | 105670 |
rs50762501 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Rcbtb2 | Mm_Celera | 14:73140032 | TTTTGGTGATGGCAG[C/G]GTGAATGGACAGATG | 105670 |
rs50782528 | snp | A/G | 0.32 | 0.24 | intron-variant | Rcbtb2 | Mm_Celera | 14:73171675 | AGCACCTGTTTGAAT[A/G]ATGTTAGTCATGGAA | 105670 |
rs50798690 | snp | A/G | 0.32 | 0.24 | intron-variant | Rcbtb2 | Mm_Celera | 14:73171429 | AGTTGTCTGTTCCAG[A/G]TAGAAGCTCCTATCA | 105670 |
rs50823108 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rcbtb2 | Mm_Celera | 14:73170773 | CTCTGCTCAACCAAA[C/T]GAGACGCTTTTAAAA | 105670 |
rs50851746 | snp | C/T | 0.32 | 0.24 | intron-variant | Rcbtb2 | Mm_Celera | 14:73171546 | CAAATCCAAAGTCTG[C/T]CAGTCCCAGTAGCTC | 105670 |
rs50878531 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73154194 | ATACTTGATAGCTTC[C/T]GTTTCAGACTTTTTG | 105670 |
rs50921607 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73165852 | CCATCTCCTTTATAT[C/T]GGCTCCAGCAGAGGC | 105670 |
rs50981704 | snp | G/T | 0.124444 | 0.216185 | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73138636 | ACTTGTATTACGTGC[G/T]TCACCAGGCTGTTCC | 105670 |
rs50991047 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rcbtb2 | Mm_Celera | 14:73140226 | TAACCCCAGGCTTTC[A/G]GCTCGTATTCCATTG | 105670 |
rs51012379 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rcbtb2 | Mm_Celera | 14:73139818 | TTACAGAGTGGGCCT[A/G]TCAGATGTGCTTAGG | 105670 |
rs51027735 | snp | C/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152917 | AAGGTATTTCCAGAT[C/G]GGTTGAGGCTGCAAG | 105670 |
rs51115145 | snp | A/T | 0.231111 | 0.249285 | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73138203 | ACAAGAAAATCATGG[A/T]TACCAGAAAACAAGG | 105670 |
rs51118586 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rcbtb2 | Mm_Celera | 14:73168631 | AGCTACTTATAAAAG[C/T]GGCCAGTTGGAAGGA | 105670 |
rs51130440 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73166344 | TACAAGTGTTCTGTA[A/G]TACGTTCTCTGCCTG | 105670 |
rs51236262 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73138191 | GATGATCATGCTACA[A/G]GAAAATCATGGTTAC | 105670 |
rs51269506 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165214 | AAGTAGAAGCCACGG[A/G]GGAACTCTACTTCCT | 105670 |
rs51281408 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Rcbtb2 | Mm_Celera | 14:73167924 | TCAGTTCTTAACCTA[C/T]TCTGTAGCAGTGATG | 105670 |
rs51285340 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73165923 | TCTGGGTAAAAGGTG[A/G]ACCTTCTCACTTCAA | 105670 |
rs51312513 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73163712 | GAAGTCTGCAGGTGG[C/T]GGACACTCTTCTGTT | 105670 |
rs51334923 | snp | C/T | 0.32 | 0.24 | intron-variant | Rcbtb2 | Mm_Celera | 14:73163867 | AGAGCTCAGTCCAAA[C/T]GCCAACTTCCTGTAA | 105670 |
rs51336841 | snp | A/C | 0.124444 | 0.216185 | missense, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73166852 | AGAGTGGCCGCCCTG[A/C]AAGGCATCCGTGTCC | 105670 |
rs51340642 | snp | A/G | 0.391111 | 0.206368 | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137032 | ACTCACATTGGCTCA[A/G]GCTTGGTTGGCGTGG | 105670 |
rs51350937 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rcbtb2 | Mm_Celera | 14:73163722 | GGTGGCGGACACTCT[C/T]CTGTTTGGGAACGTG | 105670 |
rs51370827 | snp | A/C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73154433 | TTTTTTTTTCTCTAT[A/C/T]AATAGAAAAGTCATC | 105670 |
rs51387759 | snp | A/G | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73140554 | CTAAGCAAAGCATGC[A/G]AACGAGATCACTGTT | 105670 |
rs51456867 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137964 | TTTTGTTCTGGAAGC[C/T]TTGCATTTGTGTGTG | 105670 |
rs51488962 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73145605 | ATGAGTGTGGCAGAG[A/G]GGCATTAAAGTCTCC | 105670 |
rs51493921 | snp | A/G | 0.5 | 0 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73166266 | ACTTACAAAATACCA[A/G]ATCTCAAAATGTTGA | 105670 |
rs51512059 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Rcbtb2 | Mm_Celera | 14:73166261 | ATATTACTTACAAAA[A/T]ACCAAATCTCAAAAT | 105670 |
rs51514554 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159254 | TCACTGAAGTAATGA[A/G]CTTAGTTAAGATGAG | 105670 |
rs51533625 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73157302 | ggtttagtttactgg[C/T]ttgctactagcttgc | 105670 |
rs51576945 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rcbtb2 | Mm_Celera | 14:73166961 | TTCTGCTGAAGTAAA[A/G]GCAAAGCCTTCCCCT | 105670 |
rs51587234 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73150660 | CTGAATCATTTGTGT[A/G]CCTTTTACCCCTCTG | 105670 |
rs51604750 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73147243 | AGCCTCAGGGCCCAC[A/G]GTTTGATCAGACATC | 105670 |
rs51624501 | snp | C/G | 0.32 | 0.24 | intron-variant | Rcbtb2 | Mm_Celera | 14:73168949 | TAAAGTGACTACATG[C/G]ATAAATAGAGTGCTG | 105670 |
rs51658352 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73161119 | GGCAAGTGAGTTCTA[A/G]ATGACATGGACCTTT | 105670 |
rs51667424 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73163229 | GAGTGGAATAGGAGA[C/T]TTCCTATACCCTGGG | 105670 |
rs51702049 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73167783 | GGTGCAGTAGGTGAG[A/C]CAGCTGAAGAACTGG | 105670 |
rs51706312 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73165470 | TCAGATATCTCTAGT[A/G]TATTAGTCAGGGTTC | 105670 |
rs51710134 | snp | G/T | 0.124444 | 0.216185 | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137884 | AATGCTGGCTCGGTG[G/T]CCTTTGTCACTGTGT | 105670 |
rs51732166 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159160 | TCATGCACTGTTGGG[A/G]TTTTTGTGATCCCCC | 105670 |
rs51735486 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rcbtb2 | Mm_Celera | 14:73164482 | AGATTAACTTTATGT[A/C]TTTCAATTCCACCAT | 105670 |
rs51760961 | snp | C/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73166963 | CTGCTGAAGTAAAGG[C/G]AAAGCCTTCCCCTGA | 105670 |
rs51836319 | snp | C/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73159494 | TCTCCAAAACTGTTA[C/G]TACATGTGTTACTTT | 105670 |
rs51838950 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73174436 | TCTGAAGAGGGAGTT[C/T]GACAACCCTGACACT | 105670 |
rs51878746 | snp | G/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73145066 | GCATGGCACATTGCT[G/T]CTTTTGTAAGTGACT | 105670 |
rs51918715 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73167563 | TAAGTGCATATTTCT[A/G]TATCTGAATAAGTAG | 105670 |
rs51947093 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169684 | TCCTCAGGTTCCTCT[C/T]CATTTCTATCCCTGT | 105670 |
rs51952311 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73164196 | ATTCATTCAAAGTGC[A/G]GAATCAGAAAAGGAA | 105670 |
rs51971017 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rcbtb2 | Mm_Celera | 14:73172524 | GAAAACGAGTTATTT[A/G]TCCAACCTCAGGGAT | 105670 |
rs52022434 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73157581 | CAGTAAATCTTTGTA[C/T]GTTGTGTCTCATGAG | 105670 |
rs52048441 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rcbtb2 | Mm_Celera | 14:73167619 | ATGCCGAGCCCTGAT[C/T]TTGAAAGATTTTCAT | 105670 |
rs52051542 | snp | G/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73162129 | TTCAACCACCCATAT[G/T]TTTAGTAATGGATTT | 105670 |
rs52246230 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Rcbtb2 | Mm_Celera | 14:73164974 | TAGATTCCTTTAACT[A/G]CCCCCAAAATGTGAT | 105670 |
rs52378245 | snp | A/G | 0.124444 | 0.216185 | utr-variant-5-prime | Rcbtb2 | Mm_Celera | 14:73139010 | GGAGTCACTGCAGCT[A/G]CAGAAACGAGCTTGC | 105670 |
rs52387331 | snp | A/G | 0.124444 | 0.216185 | utr-variant-5-prime | Rcbtb2 | Mm_Celera | 14:73139098 | CAGTCAAGACTCCGT[A/G]TGGTGAGTATGTGAG | 105670 |
rs52588386 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rcbtb2 | Mm_Celera | 14:73169039 | TGTACATGCTGTAAA[C/T]ATAGTCTTTTTTATT | 105670 |
rs52595794 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73165556 | ctatctatctatcaa[C/T]caatcatctatctTA | 105670 |
rs52617351 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152712 | CTCCCTCCTCCCCTC[C/T]TCCCAACTTTTCCTC | 105670 |
rs52631464 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152719 | CTCCCCTCCTCCCAA[C/T]TTTTCCTCTACTCTT | 105670 |
rs52645266 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165162 | TCCAGAGAAGTCAGG[G/T]AAGAAACTCAAGACA | 105670 |
rs52737822 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73146177 | TCAGCTCATGTCACT[C/T]ATGGAGCAACACAAA | 105670 |
rs107669002 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73151759 | ATTTACAAGGTTCTC[A/G]CTCGAAGACACTTTA | 105670 |
rs107784518 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73154031 | GACTTTCAGAGGGCA[A/G]TACTGCTTCATTTAT | 105670 |
rs108053385 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73153923 | AGACCAGGCTGGCCT[C/T]AAACTCAGAAATCTG | 105670 |
rs108385012 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73151418 | TTTTTTAATACAAGA[C/G]ATGATACAATTTAAG | 105670 |
rs211723000 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159714 | GTAACAGGCCAGATA[A/G]AAAGCTATTTCAGAA | 105670 |
rs211733259 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165701 | AAGAATCCAGTAGTT[A/C]TTCAGTCCATGAGGT | 105670 |
rs211795970 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73171231 | GCCCTGGGTCCTCCC[A/G]GCTAGCTCCCAGCTG | 105670 |
rs211854024 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73155966 | GTAGATATTGTTTCA[C/T]ATATTTCAGCCTGCC | 105670 |
rs211882586 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73171906 | GCGGAGGCGGAGGCA[C/G]AGACAGGCAGGTTTC | 105670 |
rs211959516 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178171 | CCTCCAAAGATTCTG[C/T]TGACCCAGGAGAGGG | 105670 |
rs212010401 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73183625 | CCAAGGGCTACTTTT[G/T]ATTTTCTACTTTCTG | 105670 |
rs212043652 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73139862 | ATGAGACTCCAGGGA[A/G]CTCCCTCACCCTGTA | 105670 |
rs212076318 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177812 | GAGTATTGAATAAGA[A/G]GACTCCAGATCAGTC | 105670 |
rs212139392 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73146249 | TGAGCTCAGTAAACC[A/G]AAGACTACCTCAGCA | 105670 |
rs212150954 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73153034 | TCTGATCCCTAGCAC[G/T]GAGGTGTGGGAGGGA | 105670 |
rs212161415 | in-del | -/A | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73157442 | TTGTGTCAAGTTGAT[-/A]AAAATACTGGTCAGC | 105670 |
rs212240331 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147044 | TCTTTTTTTTTTTTT[A/T]TTAGAAGTCATTTTC | 105670 |
rs212262275 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159180 | TGTGATCCCCCAAGA[C/T]TATGATCCAAAGTCC | 105670 |
rs212271331 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73152670 | AGGGGCAGCGAGGGC[A/G]GCTACCTCTGTTTGC | 105670 |
rs212394514 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177161 | AGACCTTACCACCAA[A/G]TTGGCAAATGTTGAA | 105670 |
rs212418341 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73164232 | TTTGTGGAAGGTGCG[C/T]ATATCGAGGGCTTTG | 105670 |
rs212435401 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169906 | GTTTGAAAATAGGAC[C/T]TTTGACTCCTTAAAT | 105670 |
rs212557298 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73149740 | TTCCTTAGGGTTTTT[C/T]CTCTGGTTTGCTACT | 105670 |
rs212565993 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73161796 | GCATCAGATGTGGGT[A/G]ACTCTCAGCAACACA | 105670 |
rs212604233 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73157155 | CTTAGGTTTCTGTTC[C/T]GTGAAACAACATCAT | 105670 |
rs212657407 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169409 | TTAATTGAGACTGCT[A/G]GTCCTCCTACAGGAT | 105670 |
rs212673240 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73149073 | ACTTACAGACTGGCC[A/G]TGAACTGACAATGTA | 105670 |
rs212758248 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73166464 | GCTTTGTTTATCAGT[C/T]TTTTCTTTCCCATAG | 105670 |
rs212799589 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73173693 | GTCCTCCTGTTAATG[C/T]GCCTCTGTGGCATTT | 105670 |
rs212812357 | in-del | -/A | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160430 | TCACTAATACTTTTT[-/A]AAAGATGCAAATGGT | 105670 |
rs212917906 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179929 | GAATGTCCAGTGAGG[C/T]GGCTGTGTCCACCAG | 105670 |
rs212964783 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73172836 | AGAGTGGAGGCCCTG[C/G]TGTGCTGATTGCTGT | 105670 |
rs213069700 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73161209 | GTGTAGAAACAAAGG[A/G]AAGAAATCTTACATT | 105670 |
rs213079800 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179278 | ATTTAGAGCTGAATC[A/T]GTAGGAAACAGGCCA | 105670 |
rs213143687 | snp | A/G | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141171 | TGTGTGTATAATTGC[A/G]TCACCTAAAGCAACT | 105670 |
rs213145056 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73155314 | TGATACTGTTTCCCA[C/T]CCAGTATCCAGTGAT | 105670 |
rs213157712 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147563 | GAGAATCTCAGATGG[A/G]AGAACTTGCCAGTAG | 105670 |
rs213193033 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148210 | TTAGAAACAAGCTAT[C/T]AAACTATACAAGTTT | 105670 |
rs213254595 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73154545 | GGATGGTCCCCTTAG[C/G]AGCTCCTGAACAGGA | 105670 |
rs213321754 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169926 | ACTCCTTAAATGGGG[A/G]ACAGGAGAGATAGTG | 105670 |
rs213366222 | in-del | -/TTAAG | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169880 | GTAAAAGGAGACTTT[-/TTAAG]TTAAGAGTTTGAAAA | 105670 |
rs213436055 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73182346 | TGCTGTAGCTGTATC[A/G]CGCTAACATTCCCTC | 105670 |
rs213492593 | snp | A/C | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141757 | GATATTAAACAGTAA[A/C]ATGCTCTATTTTAAA | 105670 |
rs213529424 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152431 | TATGAATACTTCCCC[C/T]TTTGAATGTGTTATT | 105670 |
rs213529626 | snp | G/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73145099 | AACATTGACAGAGTA[G/T]AGACTTGCTGGGGTT | 105670 |
rs213542019 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177277 | TTTTCTCTTTTTGGT[A/C]CTTGGATGTAGCATT | 105670 |
rs213670760 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160152 | TCAGTCTGAGTTTGT[C/T]AATATGAGCCCATTG | 105670 |
rs213751723 | in-del | -/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148565 | GCTATGGAGTATATA[-/G]TATATATGAGCCATG | 105670 |
rs213770893 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73139685 | CTTTTGATCTGCTAT[G/T]CTTTAATTTACTCAA | 105670 |
rs213774031 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73168561 | CTGGTAATGTTTGAC[A/G]TCTGCCTTCTATAGC | 105670 |
rs213799352 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177737 | AAGAGAAAAGAAACA[C/T]TAGCAAGTAACAGAG | 105670 |
rs213841622 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163465 | GCAGATCCTTTGTAG[A/C]ATGAGTTGCCTCTAC | 105670 |
rs213852240 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169100 | ATTTTAATTTTATTT[A/G]TAATTCATTTTTTAT | 105670 |
rs213922194 | in-del | -/CGTT | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73182701 | AAAGCCATTGACGAA[-/CGTT]CAACTTCTCTGTAAC | 105670 |
rs213926024 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73175681 | TTTCATACACACTAC[A/G]CATGTTCTAGAAGCT | 105670 |
rs213948627 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73145283 | TAAAGGACTTAGAGG[A/G]GACATGGATGAAGAG | 105670 |
rs213987415 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73183340 | GTTCAGTATTCAGCT[A/G]GCTGATACATAGTTA | 105670 |
rs214018228 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73174584 | TGGTGGGTAGGCAGA[C/T]AGAGCTGGCTCCCAT | 105670 |
rs214073827 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181805 | AGACCATACCTGGGT[A/G]TAGAACACTCCCTTA | 105670 |
rs214084904 | snp | A/G | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73138068 | GCAACAGTAAGCCCC[A/G]GGGACCTTTCTCTAC | 105670 |
rs214155377 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165850 | TTCCATCTCCTTTAT[A/G]TCGGCTCCAGCAGAG | 105670 |
rs214181447 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158642 | TTCCTGAAATACCCA[C/T]GAGTGTAGGGACCTA | 105670 |
rs214189391 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73166309 | AGGTGGAGAGGTAGT[C/T]TTGTGTCATATGATA | 105670 |
rs214260954 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73172019 | AACCAAACCAAAATA[A/G]TAAAACTGATAATAA | 105670 |
rs214275787 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73157871 | GGTGTCTTATTTTAT[A/G]TCTTTAATTCAGTAA | 105670 |
rs214292587 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181236 | CACTGAAGTGCTCAT[C/G]TCCCCACCTCCTTAG | 105670 |
rs214376465 | in-del | -/GCAGCAGCAGCAGCA | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73176443 | ATGCCTGGGCCACCT[-/GCAGCAGCAGCAGCA]GCAGCAGCAGCAGGC | 105670 |
rs214399503 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141054 | CATCAAAAAATGAAA[C/T]GGGGTTATCTATGAT | 105670 |
rs214457852 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73162904 | GCCTTAGCAGTGGAG[A/C]GAGAACAGTCTCTTG | 105670 |
rs214466661 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73172598 | AATCGCGTGACACTG[A/C]AGTTCCCTGTTTTAA | 105670 |
rs214471763 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147123 | ACTAAAGGTGTGTAC[C/T]AAGAGCATGTCTGCA | 105670 |
rs214506654 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73164893 | CTTGActttctctct[C/T]tctctctctctctct | 105670 |
rs214507042 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147495 | TGCAGCTTCCTTACA[C/T]ACTGATACTGTAAAC | 105670 |
rs214508486 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73140553 | ACTAAGCAAAGCATG[C/T]GAACGAGATCACTGT | 105670 |
rs214514702 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160200 | TACTATTAAACCTTG[C/T]ACCGTTCCAGGAAAA | 105670 |
rs214624969 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73180531 | GAGGAACTGGCAATG[A/G]GGGAGCCAGAAACAG | 105670 |
rs214634252 | in-del | -/GGGA | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73166887 | GTACGTCTCCTGGGG[-/GGGA]GGCGGGGGGCGGTGC | 105670 |
rs214642301 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73164872 | ATAACCAGCCCAAGC[C/T]GCCGACTTGACTTTC | 105670 |
rs214685968 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178203 | AATTCAGAGAAACAC[A/T]AACCTGTTTCATTTC | 105670 |
rs214713339 | in-del | -/TTAGAAGTCATTTTCTTTTTTTTTTTTTT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147016 | TTGTCTGCCACTCAA[lengthTooLong]TTAGAAGTCATTTTC | 105670 |
rs214731493 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73170463 | GAAAGGACCATCCTG[C/T]TCTCTGTAGTTTCCC | 105670 |
rs214737593 | in-del | -/GAG | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73175412 | CAGCCATGCTGGAGA[-/GAG]AAAAAAAAAGTGGTT | 105670 |
rs214750340 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160596 | AGGAAGTAGCATAGA[A/C]CTGCCAAAGGCAAGA | 105670 |
rs214793939 | snp | C/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73155342 | GATGCTGTTTCCCAT[C/G]CAGTATCCAGTGATG | 105670 |
rs214802710 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73164257 | GCTTTGGGGAAACAC[A/G]CTATGTTTTGGCCTG | 105670 |
rs214831395 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144481 | GTGGTTATGAGTTAA[A/C]CCGAAAAATCCCGAT | 105670 |
rs214881424 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181270 | CAGTCCTGGTGTGGG[C/T]GGGCATCCCTCCAAC | 105670 |
rs214915619 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73153152 | CTCTAGTAACAAAGG[A/G]TTGTGGTCTCCTCTC | 105670 |
rs214922132 | snp | G/T | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137353 | GGATGTAATTTCCAG[G/T]GTCATTCATCAGGTG | 105670 |
rs214923508 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144922 | CCCAGGTTGGCCTGG[A/G]ATTGAAGAGCAGCTT | 105670 |
rs215050608 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159210 | CAATACCCAGGACTT[C/G]AGTGCAATCAATTTA | 105670 |
rs215059655 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73162737 | TGGAATCATTGCGTG[A/G]CAACGCTACTTATTT | 105670 |
rs215097683 | in-del | -/A | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73171993 | GAGAAACCCTGTCTC[-/A]AAAAAAACCAAACCA | 105670 |
rs215240857 | snp | A/C | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73167121 | TTCATGCCTCTTGGC[A/C]TAAAGTAGTAAGTCT | 105670 |
rs215264496 | in-del | -/TGAT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144311 | TTTAGTGCATTCATG[-/TGAT]TGATGGTCACTGTTT | 105670 |
rs215326107 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159575 | GTTGGTTCTTAGTGA[C/T]GGTTGCTTTGAATGT | 105670 |
rs215373736 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73153797 | AAGTAATCAGAGCAA[A/G]CCTAATACATTAGAA | 105670 |
rs215401179 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141881 | TCTCTTTAAGCCCAG[C/T]CCATTGTTATAATAA | 105670 |
rs215476805 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73142376 | TACAGAGCCCCTGTT[C/T]CAAAGCCATAACATT | 105670 |
rs215548084 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148412 | AACAAACAGTGACAT[C/T]CCATAATGTTATTTT | 105670 |
rs215595073 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73157758 | AGCATCTAGCTGTCT[C/T]ACAGATTTGAAAAGC | 105670 |
rs215597633 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73164291 | AGTATGTGGGTGTTA[A/T]GATTTCTTATCCATA | 105670 |
rs215629790 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73161497 | CACGGTCCACACTTG[A/G]GTGAGTGGGTTGACT | 105670 |
rs215783342 | in-del | -/TGTG | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73183111 | TTCTTGGCTCTGTTT[-/TGTG]TGTGTGTGTGTGTGT | 105670 |
rs215799710 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73174200 | AAACAGTTGGGAACA[C/T]TTTTGGCTTTGGCAA | 105670 |
rs215822680 | in-del | -/TGAGTGTGTG | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73183110 | TTCTTGGCTCTGTTT[-/TGAGTGTGTG]TGTGTGTGTGTGTGT | 105670 |
rs215831804 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73139767 | ATATGAATGGTGGTG[C/T]CTTTTCTTTTTCATG | 105670 |
rs215934544 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73182664 | AGATAAATAAATAAA[G/T]GAATAAATAGTAATT | 105670 |
rs215996139 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158699 | ATGTGAGATTTAAAA[A/G]CAATGCCAGATTCCA | 105670 |
rs216052209 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148952 | GGCAGAGGGAATCTT[A/G]GTTTAGAAGTCATCA | 105670 |
rs216065497 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163574 | ACTAAGGCACCGTGG[A/C]TGTGGTGAAAGACAC | 105670 |
rs216073846 | in-del | -/GGCAGAG | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148937 | ATTTGTTTTTAAAAT[-/GGCAGAG]GGAATCTTGGTTTAG | 105670 |
rs216098978 | snp | G/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73163794 | AGCGTAGCCTTGCTT[G/T]CTCATGTGGAAAAGG | 105670 |
rs216101057 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158173 | GACTCTGTGAGCGTG[C/G]TGTACTGGGCCCTGA | 105670 |
rs216248769 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181743 | ACAACAGAGACAGAA[C/T]TTTAAACTTTGAATA | 105670 |
rs216256365 | snp | A/G | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137984 | ATTTGTGTGTGGGGG[A/G]CCGAGTATGCATGGG | 105670 |
rs216291119 | in-del | -/TTGTTG | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73154213 | TCAGACTTTTTGTTA[-/TTGTTG]TTGTTGTTGTTAAAG | 105670 |
rs216340245 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179954 | CACCAGTAGGTGGTA[A/G]GGGTAGCCCCACCCA | 105670 |
rs216424725 | in-del | -/ATCTC | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73172981 | GAATCCCTTCAGTAG[-/ATCTC]ATTCTGTCAGCATGC | 105670 |
rs216437601 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160636 | TTATCACCATAATGG[A/G]CATCACAGGTAAAAC | 105670 |
rs216440851 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73173786 | GACACAAGGTGGGCA[C/T]GTGTACATGTGGGGC | 105670 |
rs216444491 | in-del | -/A | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73162113 | ATTTGGAAGAAAAAA[-/A]TTCAACCACCCATAT | 105670 |
rs216469746 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73170520 | CGTCAGGCAGGCCTC[A/G]GTCGCAGGCCTGTGG | 105670 |
rs216474931 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73155747 | GATGCTGTTTCCCAT[C/G]CAGTATCCAGTGATG | 105670 |
rs216627819 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179125 | ATGAATGAGAGAAGC[A/G]GGAGATGATTCTGTC | 105670 |
rs216668825 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73145732 | GACTCTTCTCGCTTC[C/T]CTTATCTGGAAGAAG | 105670 |
rs216695201 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141109 | AGGGATTGGTTGGTA[C/T]GAAGAGTTCAATGTC | 105670 |
rs216776491 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141537 | GGACTGTTGAATTCT[C/T]TATCACTTTAAATGG | 105670 |
rs216794668 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159002 | GGCACCAATGGAGTC[A/G]TGATGGGAGAGAATT | 105670 |
rs216820197 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73152626 | AGTCACGGATGGAGG[G/T]TCCCTTGCTGCTGGC | 105670 |
rs216831392 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73156267 | ACAAAATGTAGTAGA[A/G]GACTGACTGGAGAGA | 105670 |
rs216927076 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160077 | GCTGAAGTCTAGGGA[A/G]CGTGTGTGACCATGG | 105670 |
rs216957188 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178112 | TCCCAACCCAACCGG[C/G]TTTCTTTTTAATTCC | 105670 |
rs216962064 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73146138 | AAATTACCTCTCAAA[A/T]GGACTTACAGATGGC | 105670 |
rs216991630 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165071 | AAAAGCAACTTGGGG[A/G]AGAAAGAGGTTTTTG | 105670 |
rs217024188 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159651 | GGAAGTGTCCCGATG[A/G]TCTTGATTGGTGTAG | 105670 |
rs217032716 | in-del | -/TGGAG | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148561 | ACCTGCTATGGAGTA[-/TGGAG]TATATATATATGAGC | 105670 |
rs217074060 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169301 | GAATGAACACAGAAC[C/T]GGAAGTCCTCTACTG | 105670 |
rs217085772 | in-del | -/AGCAAG | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73142309 | TGAGGGCAAAGATCA[-/AGCAAG]AGGAGGAGGGATGGA | 105670 |
rs217111301 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73176416 | CAGCAGTAGGCTGCA[A/T]TGTAGAGTCAGATGC | 105670 |
rs217114472 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73182223 | AAGGTGCTGGAGGAT[A/G]CCTAGCTTAGGTTCC | 105670 |
rs217233021 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181778 | CAGGTGGTGGTACCT[C/T]TGTGCTGAGTCAGAC | 105670 |
rs217266270 | in-del | -/A | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73154056 | TTTATACTGTGGTTG[-/A]AACCACAGTGGAGAG | 105670 |
rs217295295 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158101 | AAAGGAGAAACAGCT[A/G]AGGTAGTTAGTAACC | 105670 |
rs217317445 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73151957 | ATTCTAAGTTCTGAT[C/T]TGACCAGGTAGTGCT | 105670 |
rs217345450 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169813 | CATCAACGCTCCCTC[C/T]CTCTGAGTCCTGGGA | 105670 |
rs217355290 | in-del | -/C/CC | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73171033 | AAGCAGCAGCAACAA[-/C/CC]CCCCCCCCCCTTTTA | 105670 |
rs217386944 | in-del | -/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73168517 | TGCTTTCTCCCCTTG[-/T]TTTTTTTATTTTTAT | 105670 |
rs217397902 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158948 | AGACATTTTTTTCTT[C/T]ATTTAATGAGTACTG | 105670 |
rs217408233 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73174309 | TCAGCATTTCTGGAA[G/T]GCCCAGCGAGTAGGG | 105670 |
rs217430723 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73176347 | AGAGATCCCCCGTCT[A/C]CCCCAGTCCAGCAGG | 105670 |
rs217464980 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73162290 | TCAGAAATGGAGTTC[C/T]TTGAACTGCCTGGTT | 105670 |
rs217466657 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73175334 | ACACAGGTCTGCAGA[C/T]AGCCCTGAACACAGC | 105670 |
rs217523970 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73180488 | TGTTGCAGTAGAGCC[A/C]TGCGGAAAGGCCTGA | 105670 |
rs217557884 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73175894 | GGTTCACTCTCACCA[C/T]GGAGCCTCTACTTTC | 105670 |
rs217618624 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73180028 | TATACTTGATGTCTT[A/G]GATGTGGGATGGGGA | 105670 |
rs217642669 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73166977 | GCAAAGCCTTCCCCT[G/T]AACTAAGGTGCAGAT | 105670 |
rs217739171 | in-del | -/CCAGCAAGGA | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73155045 | TAGGATGTGGATGGG[-/CCAGCAAGGA]GCTGATGTCACCTAG | 105670 |
rs217743748 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148990 | TATTCTATGAAATTC[C/T]TGTGTTCATGGTAAA | 105670 |
rs217810908 | in-del | -/ACAT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165583 | CTTATCATCGCACAC[-/ACAT]ACACACACACACACA | 105670 |
rs217852112 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73153329 | AAAATGAGGATTCCA[A/G]CAGATCTGCTGAAGT | 105670 |
rs217868579 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73170651 | CTGGGGCTCCTTCCA[G/T]CGAAGCCTAATTAGG | 105670 |
rs217910029 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158997 | TTCGAGGCACCAATG[A/G]AGTCATGATGGGAGA | 105670 |
rs217926700 | in-del | -/TCATTCTTA | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158860 | TGAAAGTAGAAGGTG[-/TCATTCTTA]GCATAGGGCTTGCAA | 105670 |
rs217935191 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177440 | ACAGGCAAGCATGGA[A/G]GGAAGGGCAGATGGC | 105670 |
rs217949322 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73156360 | TCTTGGTTCACAATC[A/G]TCTATAACTCCAGCT | 105670 |
rs217985566 | in-del | -/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73151403 | GTATCTCCACTGCTA[-/T]TTTTTAATACAAGAC | 105670 |
rs217997288 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181911 | TACATATGTAATTCT[A/G]TAAAAATTACTTTGG | 105670 |
rs218031806 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73176709 | CATATCTTGGTGGGA[A/C]CTGCCTACTGGAACC | 105670 |
rs218114427 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73156544 | acacacacacacaAC[A/G]TGTGAATAGAAAAAC | 105670 |
rs218132323 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73172658 | TCACTCATTTCCCTG[A/C]GGTTTCGTTGAACCG | 105670 |
rs218260823 | in-del | -/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179446 | GGATTCTAAGTCTGC[-/G]GGAGGAAACAATGCA | 105670 |
rs218263249 | in-del | -/TGCGTGAAA | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73149078 | AGACTGGCCATGAAC[-/TGCGTGAAA]TGACAATGTAGCTAG | 105670 |
rs218326204 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73157971 | ACCTCATTCACACAG[A/C]GGAATCTTCCTGTTC | 105670 |
rs218343048 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147526 | CCTGCTCTCCTGCAC[C/T]GCCTGCCTTTGACTC | 105670 |
rs218397950 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73173378 | AACTCAGAAATCTGC[C/G]TGCCTCTGCCTCCCA | 105670 |
rs218439953 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148576 | ATATATATATATGAG[C/T]CATGTTGTATAGCCT | 105670 |
rs218465952 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147217 | TTTCTCTTTCTCTTT[C/T]TTCTGTAAATAGCCT | 105670 |
rs218481091 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73154469 | GATGGGAACTCCTGA[A/G]CACTTCCTTGTAGAC | 105670 |
rs218532305 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73155882 | GTAGATATTGTTTTG[C/T]ACCCTATATCCAGTG | 105670 |
rs218534455 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147911 | AAATGAACATGTGCT[C/T]CATCATCACCTTAAC | 105670 |
rs218665187 | snp | A/G | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73138027 | TATTCATTCAGATGC[A/G]TGTGCCCCCTGATGC | 105670 |
rs218682430 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73154802 | CATGTGGCCTGGCCT[C/T]CTGATTTTACCATGT | 105670 |
rs218682853 | in-del | -/TTTTTT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73154297 | TTCATTCATTTCTCC[-/TTTTTT]TTTTTTTTTTTTTCC | 105670 |
rs218745989 | snp | G/T | | | utr-variant-5-prime | Rcbtb2 | Mm_Celera | 14:73138802 | ACACTGTCAAGAATG[G/T]CCCGGTGTGATCAAC | 105670 |
rs218789874 | in-del | -/GGATGGATGGATGGAT | | | downstream-variant-500B | Rcbtb2 | Mm_Celera | 14:73184346 | TAGATATGGAAGGAA[-/GGATGGATGGATGGAT]GGATGGATGGATGGA | 105670 |
rs218894841 | snp | C/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73150486 | CTGCACTTGGGACCA[C/G]ACTGAACACATGAGT | 105670 |
rs218986201 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144537 | GGAAGAGCAGTGACA[C/T]CTGTCACAGTGGCAG | 105670 |
rs219105237 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73162855 | TTAGCAGTCTGTGCT[G/T]CTTTCATTAAGTAGT | 105670 |
rs219170151 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73146745 | ACTGACTGAATTGTT[C/G]TGCTTGGCCTCATAT | 105670 |
rs219257085 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73168482 | GAACTGTCACTCGCA[A/G]TTCTGTGGCTGTCTT | 105670 |
rs219265319 | in-del | -/ATGTCCC | | | utr-variant-5-prime | Rcbtb2 | Mm_Celera | 14:73138798 | TAGACACTGTCAAGA[-/ATGTCCC]ATGTCCCGGTGTGAT | 105670 |
rs219266435 | in-del | -/AACCAACC | | | utr-variant-5-prime | Rcbtb2 | Mm_Celera | 14:73139029 | AAACGAGCTTGCCAA[-/AACCAACC]AACCAACCAACCAAC | 105670 |
rs219321086 | in-del | -/ACAT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73149663 | TGGTATGTTTGTGCC[-/ACAT]ACGGGTTGTCAGTCT | 105670 |
rs219331829 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73168790 | CTTCTTTGGATAGTC[A/G]CGTAACTGTCTTTTC | 105670 |
rs219370763 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73167865 | AGTACTTGTTAATGT[A/C]GTGGTGGCCTTTATG | 105670 |
rs219409872 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169570 | GGGCAGTCATAATAG[A/T]TCCCTTTTTGTGAGT | 105670 |
rs219455775 | in-del | -/AAA | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73167123 | ATGCCTCTTGGCATA[-/AAA]TAGTAAGTCTACTTT | 105670 |
rs219474480 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73176005 | TCATATGAGCAGTAT[C/G]GTGTTTTCTCTGAGG | 105670 |
rs219487823 | in-del | -/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165650 | CTATGTAGGCTATAG[-/C]TTGTACAACAAAGAC | 105670 |
rs219517085 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73150742 | AGGGGATACAGATGA[A/C]TCCTGTGATGAATAT | 105670 |
rs219542909 | snp | A/G | | | intron-variant, utr-variant-5-prime | Rcbtb2 | Mm_Celera | 14:73143606 | CGCAGCCGCCTCGCC[A/G]ACCCCATGGCGGCAC | 105670 |
rs219552323 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144570 | CTGTAGGACTCAGGA[C/T]GGAGCATCGAAGTAT | 105670 |
rs219586773 | snp | C/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73142515 | AGCCCCACAGGCTCC[C/T]TTCTCCCTAGTCCCA | 105670 |
rs219616543 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73150241 | TCCCAAGATCCAGCA[C/T]TGTCTCCTGGCCTTT | 105670 |
rs219617892 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73168079 | TGGCCAGTTGGGCAC[C/T]GGCAATAAAAGTAAC | 105670 |
rs219657570 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73173929 | GTAAGCTTGTCCTTT[C/T]CCTCTTGGGACAGTT | 105670 |
rs219660856 | in-del | -/GGGGGCGGGGGGGGGGG | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73161326 | AAGACTAGGTCTCCC[-/GGGGGCGGGGGGGGGGG]GGGGGACCATGCTAG | 105670 |
rs219780476 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73149588 | CTGGAAGAGCAGAAA[C/G]CTGCACTCTTAACTG | 105670 |
rs219868191 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159297 | GGTACTAATCCAGTC[C/T]GACTTGGGTGTTTCT | 105670 |
rs219942683 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165177 | GAAGAAACTCAAGAC[A/G]GGAACCTAGAAGCAA | 105670 |
rs219966597 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147389 | ATACTTACATTACCT[A/G]TAACTCGGGGATGAC | 105670 |
rs219987513 | in-del | -/AGAG | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73143960 | TTTGTTGTGACAATC[-/AGAG]AGATTTAATAAATGT | 105670 |
rs220001730 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147689 | TTTCTCTGAGGAATG[C/T]CTCCTCTTTTTAAAT | 105670 |
rs220001858 | snp | A/G | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73140847 | GCTGAAGAAACTAAA[A/G]CGTCGCCTGCCCTTT | 105670 |
rs220016321 | in-del | -/AAAC | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73150568 | ATTAAATAAATAAAT[-/AAAC]AAATAAATAAATAAA | 105670 |
rs220046440 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73164575 | AAGGGAAGCCAAGCA[C/T]CCTCTGCAGCTGAAT | 105670 |
rs220116407 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73170232 | ATGAGAGCACATCTT[C/T]CCACTGGCTCACTCT | 105670 |
rs220194889 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73146488 | ACATTATTTTTATTC[A/G]CTAGATGTAATTGTC | 105670 |
rs220208276 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73182810 | CTACCCCGAGATTTA[C/T]AGTAGCAGGCACTGA | 105670 |
rs220222079 | in-del | -/GG | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148237 | TTTAAGAAAACAGCT[-/GG]GGAAAAAAATAGCAA | 105670 |
rs220241947 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73164048 | ATTATTGTCAAGTGA[A/G]CCTTGACTGGACAAA | 105670 |
rs220246917 | snp | A/G | | | utr-variant-5-prime | Rcbtb2 | Mm_Celera | 14:73139096 | AACAGTCAAGACTCC[A/G]TGTGGTGAGTATGTG | 105670 |
rs220272045 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73145448 | CCTTTGTCCATTGGA[G/T]ATTATCATATTTAAT | 105670 |
rs220272699 | in-del | -/TC | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73171820 | CTTGAGTTTTTTTTT[-/TC]CCCTTAAAAATACAA | 105670 |
rs220371767 | snp | A/C | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152171 | GCTATAACCCCCCCC[A/C]CACACACACACACAC | 105670 |
rs220487547 | in-del | -/TGCCC | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73159797 | ACACCAACTTGGTTT[-/TGCCC]GTCACTGCTGCCGAT | 105670 |
rs220510263 | snp | C/T | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73138311 | CCATTGCTTTCTGAC[C/T]TATGACTGCTGGCAT | 105670 |
rs220572040 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73158053 | ATGGTTCAAGTGAAT[A/G]ACTTGTAGACAAGTG | 105670 |
rs220669289 | snp | A/G | | | intron-variant, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73142934 | GCCGATCCCGGCCGA[A/G]GAGGGAGGCGGGGCG | 105670 |
rs220734587 | in-del | -/AC | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73182932 | TGTAAATAGCTTTGT[-/AC]GGGTAGGTTGGTGGG | 105670 |
rs220773570 | in-del | -/GTGATAGAGATTCATGCAGATCC | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163435 | AAGTATATTAAGAGT[-/GTGATAGAGATTCATGCAGATCC]TTTGTAGCATGAGTT | 105670 |
rs220808452 | snp | A/C | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141939 | TGAACTTTCAGCCTC[A/C]GGAACCGTGAACTTG | 105670 |
rs220829647 | in-del | -/TT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73175657 | CTGAGCAGCCAATGA[-/TT]TTTTTTCCTTTCATA | 105670 |
rs220843135 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179786 | CACTAGGCCTAACTT[A/G]TATATATTTTTAAAT | 105670 |
rs220970579 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73161245 | GCAGTAATGGGGATT[A/C]ATGGCCCATCAGTCA | 105670 |
rs221051012 | snp | C/T | | | intron-variant, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73142918 | CAGAGAGGCCAGGGT[C/T]GCCGATCCCGGCCGA | 105670 |
rs221055414 | in-del | -/TCTC | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165959 | TTAATCAAGTAAGAG[-/TCTC]TCACAGCTGTGTCCA | 105670 |
rs221074751 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160723 | ATGACCAAAAAGCAA[C/G]TTGGGGAGAAAGGGT | 105670 |
rs221090810 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73180097 | GGCTGCGTAACTGAA[A/G]AGATGAACAGTCTTA | 105670 |
rs221211295 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165981 | CAGCTGTGTCCAACC[A/G]TTTGCTTTAGTTAAT | 105670 |
rs221398618 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141239 | TGCCATCCAGGGTAC[C/T]ATGGGGATGCAGCAA | 105670 |
rs221412088 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181835 | AGAAAGCCTACTCTG[C/T]CCGAGGATTTAAGCC | 105670 |
rs221417832 | snp | A/C | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73140800 | GAGCATTTTGTTCAG[A/C]ACCCTGCTGTTTCAG | 105670 |
rs221489336 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181512 | GTTATGGGATGGCAT[G/T]ATTACATTTCCCTTG | 105670 |
rs221545588 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163717 | CTGCAGGTGGCGGAC[A/G]CTCTTCTGTTTGGGA | 105670 |
rs221612846 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73162996 | TGCCAGGATAGGCCC[A/G]ATTATTCAGACCATT | 105670 |
rs221634901 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163958 | TAGAATATCAGACAA[A/G]ATGGCAGAAAAGAAA | 105670 |
rs221658671 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73168188 | AATTAAACAGCTCTT[C/G]GAATTCATAGTGTAG | 105670 |
rs221659639 | in-del | -/AATA | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73174928 | TGTAGCTTAGTGCTG[-/AATA]AATAAGTTTTGCCCT | 105670 |
rs221672905 | in-del | -/CT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73152571 | AGGATACAGCTAAGA[-/CT]TCCTTTTTTTTTTTT | 105670 |
rs221719690 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73162637 | ATGAAGCAGGACGGT[G/T]CTGGAGCAATGGGGC | 105670 |
rs221754745 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178880 | GCACCATGGACAAGC[A/T]CCATACATGTGCTGT | 105670 |
rs221783394 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73176520 | AAAGCAAGGAGCCAA[C/G]GCAATGACAAGGTTT | 105670 |
rs221790235 | snp | G/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152252 | TCTCTGTCGTAGCTG[G/T]TACTTTGACATGGTA | 105670 |
rs221860295 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160226 | GAAAAAGACAAAGGT[A/T]CCAAGAGTTTATTTG | 105670 |
rs221866284 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73154046 | ATACTGCTTCATTTA[C/T]ACTGTGGTTGAACCA | 105670 |
rs221868324 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165404 | AAAAATACCTTACAG[A/G]CTTGCCTGCCACCAT | 105670 |
rs221940910 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144694 | GCTCAGAAAAACTAC[A/G]TAGCCAACTTTCCGT | 105670 |
rs221960655 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159859 | TTCCAAGTATCTGCT[C/G]TGGACTAGGGACCAC | 105670 |
rs221974608 | snp | G/T | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137606 | GACGAACTACATGAG[G/T]AAGTACCTGCTTGAT | 105670 |
rs222080441 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73180870 | CGCTCGCATAGTCAG[A/G]GTAAGAGGAAGTATT | 105670 |
rs222110406 | snp | A/G | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73140681 | AAATCTGCTCTGCTC[A/G]TCCTAGCACCCCACC | 105670 |
rs222113121 | snp | A/G | | | downstream-variant-500B | Rcbtb2 | Mm_Celera | 14:73184076 | TTCTTAAATTGTTGA[A/G]TAACAAAATCAAAGT | 105670 |
rs222125002 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73140271 | TTTTAGAATAGACTC[C/T]TTCCTAAGGACAAGG | 105670 |
rs222210874 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73140145 | GTTGAGGCAAAGGGC[A/G]GACTGTTTACCGGAA | 105670 |
rs222259119 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163704 | AAAGGACTGAAGTCT[A/G]CAGGTGGCGGACACT | 105670 |
rs222282748 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73156754 | TCTTCTATATAGACT[A/G]TAGTTTAAACTGAAT | 105670 |
rs222296036 | in-del | -/AGAA | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137938 | ACAGAGTCATTCTAT[-/AGAA]AGAAAGGTTTTGTTC | 105670 |
rs222450036 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73161386 | TATGCTCTTTAAGAC[C/T]CTCCTTCCCCAGCCT | 105670 |
rs222463851 | in-del | -/TC | | | utr-variant-5-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73154357 | CTGAGAGCTGATAAG[-/TC]TCTTCTTCACCGTGA | 105670 |
rs222482072 | snp | C/T | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137394 | TTTATCTAACTAAAG[C/T]ACAGACCAGCAGATG | 105670 |
rs222553835 | in-del | -/T/TT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73167969 | ACTTGTAGACTTGAC[-/T/TT]TTTTTTTTTTGTCCT | 105670 |
rs222581677 | in-del | -/TG | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165104 | TTTTTTTTTGTTTTT[-/TG]TTTTTTGTTTTTTTT | 105670 |
rs222584256 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181432 | ACTATTCCGTTTTGT[C/T]TTCAAGAGCTCATGT | 105670 |
rs222591918 | snp | C/T | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73136796 | TTTGAGATGTACCTG[C/T]GATCATCAGTCCAGA | 105670 |
rs222700463 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73162609 | CTGTGAGCTTGGCCA[C/T]GCGTTGGGCAACATG | 105670 |
rs222742369 | in-del | -/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73172001 | CCTGTCTCAAAAAAA[-/C]CAAACCAAACCAAAA | 105670 |
rs222831485 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73159801 | CCAACTTGGTTTGCC[C/T]TGTCACTGCTGCCGA | 105670 |
rs222846189 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178012 | AGGCAGATGTGCCCA[C/T]GACAGGGGATTCCTT | 105670 |
rs222859336 | in-del | -/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73151359 | TATCCAGAAGTTGCA[-/T]TTTTATCATTTTAAT | 105670 |
rs222879886 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73153985 | AGGCGTGCGCCACCA[C/T]GCCCGGCTCTAGATA | 105670 |
rs222885414 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178237 | GAAAAATTATTCAAG[C/G]CATTCTGATGTTAAC | 105670 |
rs222966879 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73183951 | GTAGCACTGGATTCC[A/T]CCAAGTGTCTCACAA | 105670 |
rs223042224 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159275 | TTAAGATGAGGTCAT[A/T]AAGGTTGGTACTAAT | 105670 |
rs223094637 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73153389 | GCAAAAATATTTTAC[C/G]AAGTCAAATCATGTA | 105670 |
rs223229376 | in-del | -/A | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73150330 | TAAAATTAAATACAT[-/A]GGGGTGTGTGTGTCA | 105670 |
rs223244454 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177943 | CTCTGAGAGACTGCT[C/T]TCCAGGAGTGATGCT | 105670 |
rs223260375 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73174954 | TTTGCCCTTGGAACA[A/G]AGCCAGATGCTCTGA | 105670 |
rs223261412 | in-del | -/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73145913 | TTCTTCCCACCCCCA[-/G]TACACTTTTGAGCTA | 105670 |
rs223291764 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73175955 | ACAGAGCAAACACTG[A/T]ACACGCTCAGCCTAC | 105670 |
rs223357394 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73180734 | CAGGAGGTAGGCCTT[A/C]TATTAATCATGGACC | 105670 |
rs223381362 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73183755 | TTTCTTTATATTGAG[G/T]GTCTCTCTATATAAG | 105670 |
rs223413043 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73157340 | TTGCTTCTGGCTTGC[C/T]CAATTTGTTTTCTTA | 105670 |
rs223518023 | in-del | -/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147196 | ACACCACAACTAGAA[-/T]TTTTTTTTCTCTTTC | 105670 |
rs223537641 | in-del | -/A | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73174249 | AAGGCGTGAATCCAT[-/A]CCCAGAGGCAAAAGC | 105670 |
rs223539596 | snp | A/C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73176110 | GTAGCATTCTCCGAG[A/C/T]CTGCCTGTGTCCCAG | 105670 |
rs223559670 | in-del | -/TTC | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73171819 | CCTTGAGTTTTTTTT[-/TTC]CCCTTAAAAATACAA | 105670 |
rs223564825 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160816 | TCAAGCAGGGCTGGA[A/G]CCTGGAGGCAGGAGC | 105670 |
rs223619177 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73158875 | GGCATAGGGCTTGCA[A/G]CTAGCCTGAGGAAAC | 105670 |
rs223627077 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181576 | CCTATGGGTTCGTGT[A/G]CATGTTGGCATGGCT | 105670 |
rs223633734 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73182892 | CCACTCTTGTGGGGA[A/G]TCTCCCTCTCCCAGC | 105670 |
rs223639671 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73175393 | AACACAGCTGGATTC[A/G]GATACAGCCATGCTG | 105670 |
rs223664274 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73139367 | GGCCAAGGAACCAAC[A/G]TTAGTTTTGGTGGGT | 105670 |
rs223694714 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177495 | CCTAGAAGATCTCTT[C/T]GTCATTGCCCCAGAG | 105670 |
rs223705604 | in-del | -/AAAAA | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73175411 | ACAGCCATGCTGGAG[-/AAAAA]AAAAAAAAAAGTGGT | 105670 |
rs223735886 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181162 | ACCTAAGTGGTAGTT[C/T]CTTAGGAACATTTGG | 105670 |
rs223799380 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73149665 | GGTATGTTTGTGCCA[C/T]GGGTTGTCAGTCTGT | 105670 |
rs223904270 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73180200 | ACACTAGGAATCTGG[C/T]CTCAAGGGTCTGTGA | 105670 |
rs223919866 | snp | A/C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73174664 | ATGTTTAAAATAATT[A/C/T]GTAAGAGCTGGTCTC | 105670 |
rs223951736 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73174025 | GAACCTCTTTCTGGG[A/G]GCCCTTGGGGAGGGG | 105670 |
rs223968431 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73158363 | TATGCCACGTTTCAA[A/G]TCTTACTCTTCTTAA | 105670 |
rs224017004 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73180601 | AGATTGAAGGGCCGG[C/T]TGAGATAATCAATGC | 105670 |
rs224069197 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73149131 | GACCTTCCTAAGGAC[A/G]GGGATCGTAGGTGTG | 105670 |
rs224084839 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73171918 | GCAGAGACAGGCAGG[A/T]TTCTGAGTTCAAAGC | 105670 |
rs224115051 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158516 | CTGTGAACCAGCTTT[C/T]AGCAAGTCACTCTTC | 105670 |
rs224143553 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73172569 | TAGCCACACTTCCCA[A/G]ACAGGCCTATTGAAA | 105670 |
rs224158775 | in-del | -/A | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73170737 | TAGAGAAAGAAAAAT[-/A]AAACCTATGTACACT | 105670 |
rs224168347 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148701 | AGGTGTGACACTGTT[A/G]CTCTGAAGAGTTGTC | 105670 |
rs224185280 | in-del | -/TCAA | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169043 | ATGCTGTAAACATAG[-/TCAA]TCTTTTTTATTTTTG | 105670 |
rs224284246 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73154276 | CTTCAGCTGTTCATT[C/T]ATTCATTTCATTCAT | 105670 |
rs224284359 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147104 | TTTACCTTCATTGTT[C/T]GGGACTAAAGGTGTG | 105670 |
rs224305438 | in-del | -/TT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163000 | GGATAGGCCCGATTA[-/TT]TTCAGACCATTTCTT | 105670 |
rs224342341 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73172987 | CCTTCAGTAGATTCT[C/G]TCAGCATGCAGAAGT | 105670 |
rs224407431 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147468 | GGGACCCCCATGGTC[A/G]TTCACTTTGTCTGCA | 105670 |
rs224448686 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73153758 | GACTCTGTGATAGCA[A/G]TGCTTGCAAGATGCG | 105670 |
rs224482462 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73179446 | GGGATTCTAAGTCTG[C/T]GGAGGAAACAATGCA | 105670 |
rs224571105 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73172272 | TGCAGGGCCATTCCA[A/C]AGAGCACCAGCTGTG | 105670 |
rs224576626 | in-del | -/TAGT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73173622 | TCCACCTCTGTCAGC[-/TAGT]TAGTCGGCACAGTCT | 105670 |
rs224688333 | in-del | -/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73152572 | AGGATACAGCTAAGA[-/T]CCTTTTTTTTTTTTT | 105670 |
rs224698510 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178821 | TATGGAAGGAGAGAA[A/C]TGTCTCCAAATTGTC | 105670 |
rs224722353 | in-del | -/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169076 | TGTACATTTTATTTA[-/T]TTTTTTAAATTTTAA | 105670 |
rs224766777 | in-del | -/TAC | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73161918 | GGTTGTCTCAGTATA[-/TAC]TAAGTCTGATTCCTT | 105670 |
rs224868202 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169658 | ACTTTGGGCCTGTCG[C/T]TGGACCTTTTTCCTC | 105670 |
rs224979064 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73176613 | GCTTACTTGGTGCGG[A/C]TGAACTGTAACTCCA | 105670 |
rs225074719 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177386 | AGGTTGAGTGGGTAG[C/G]TCTAGTAAGAGGTCA | 105670 |
rs225119521 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73157950 | GTAGGACTGCAGATT[G/T]CATGAACCTCATTCA | 105670 |
rs225234136 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73161302 | ACCCAGAACCCCTTG[A/G]ATGAAGGGAAGACTA | 105670 |
rs225254933 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73171084 | ATGTGGAGTTCACTG[C/T]AGCACGGCTTCAGCC | 105670 |
rs225295389 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73152067 | GAGAATAAATGAAGC[A/G]CACTCTAAATGTCAG | 105670 |
rs225330052 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177678 | CCAGGTCATGCCCAG[A/G]GAAAATAGCCTAGCC | 105670 |
rs225337363 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73145239 | GGTGGTTTTATATGA[A/G]CCAGACAAATGTAAG | 105670 |
rs225356266 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73156656 | ACAAAACGTTACCTC[C/T]AGAAAATCTACAAAA | 105670 |
rs225425562 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148484 | TGCAGAGCGTACTAT[G/T]GACTATGTAAATAAG | 105670 |
rs225467498 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141912 | GTTCACAGACTGTTG[C/T]TTAGCCTAAGCTGAA | 105670 |
rs225658753 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73168355 | TGAGTTTGAGACCAG[C/T]CTGCTCTACAGAGTG | 105670 |
rs225661181 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73166911 | GCGGTGCACCAGAGC[A/C]GAGTGTCCTCATGCA | 105670 |
rs225700226 | in-del | -/AGTT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159143 | GGCATATGGTCATGA[-/AGTT]ATCATGCACTGTTGG | 105670 |
rs225715362 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73168710 | TGAAGTGTTAGAAAA[C/T]GAGAATTCAGTTTTA | 105670 |
rs225765272 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141295 | ACTCTTGTTTGTTCG[C/T]TTTGTTTGTTTCTTC | 105670 |
rs225770788 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73175110 | AGCCCTGAACACAGC[A/C]CTGCAGACAGCCCTG | 105670 |
rs225770928 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165888 | TCCAGGTCAAAGGTA[A/T]ATCTTCCCACCTCAG | 105670 |
rs225825808 | in-del | -/C | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73138086 | GACCTTTCTCTACTA[-/C]TCTCTACTTATTATT | 105670 |
rs225833855 | snp | C/T | | | intron-variant, utr-variant-5-prime | Rcbtb2 | Mm_Celera | 14:73143389 | CTCTGGGTTCACGTC[C/T]CTTCCCGGGCCCTGG | 105670 |
rs225882525 | in-del | -/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73176382 | TTGTAAAGTCAGCTG[-/C]CTGGGCCGCCCACAG | 105670 |
rs225888784 | in-del | -/AGCCCTGCAGAT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73175215 | GATAGCTCTGAACAC[-/AGCCCTGCAGAT]AGCCCTGCAGACAGC | 105670 |
rs225909393 | in-del | -/A | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73162107 | GAGGTAATTTGGAAG[-/A]AAAAAATTCAACCAC | 105670 |
rs225922371 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148819 | GCAGAAATAGAGAGC[A/C]TTTGTGTTATCCTAG | 105670 |
rs225932966 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147723 | CTTCTGAGATTACTT[C/T]TCATAGATAACTATC | 105670 |
rs225960204 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73142335 | GAGGGATGGAGGCTA[C/T]GATGTTTGAGGCTAA | 105670 |
rs225960290 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73149309 | GGTTGTCATGCGCAG[C/T]ACATTAACTGAGGAT | 105670 |
rs225987625 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73170897 | CTGTGGCCTCTTGAG[A/G]TCTTTAGTAGTCCAC | 105670 |
rs226105871 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165266 | TCAGCCTACTCTCTT[C/T]ACTTGATCTTAGCCA | 105670 |
rs226146719 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73156715 | ACATTGTTTTACTAG[C/T]CATGCCCAACATGAT | 105670 |
rs226177148 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163768 | TGTCTTGGTCTCTCT[A/G]GTCAGATGACAGCGT | 105670 |
rs226190534 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73145940 | GCTAACAAGTGCTGA[A/T]GAATGATAGCTAAAC | 105670 |
rs226191455 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73155315 | GATACTGTTTCCCAC[C/G]CAGTATCCAGTGATG | 105670 |
rs226240461 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73140358 | GACTTTGTAACTGGA[C/T]ATCAGTCCATTCCTG | 105670 |
rs226257732 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169101 | TTTTAATTTTATTTG[C/T]AATTCATTTTTTATA | 105670 |
rs226286375 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73171410 | CTTACTTGCCCCTAC[A/T]CTGAGTTGTCTGTTC | 105670 |
rs226295633 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169804 | CAGGCATTTCATCAA[A/C]GCTCCCTCCCTCTGA | 105670 |
rs226307420 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73156216 | TAGGAATTTATAAAA[A/G]TAACTTACAAACTAC | 105670 |
rs226319918 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73146061 | ATGTTGTTGAGCCAA[A/G]TCTTTAATAGGATAA | 105670 |
rs226355941 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73146855 | AACTGTAACTCTCCC[A/G]GTAGAGCTGCCTCCT | 105670 |
rs226357562 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73139754 | TCTCGAGTGTGTTAT[A/G]TGAATGGTGGTGTCT | 105670 |
rs226371263 | in-del | -/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73162310 | CTGCCTGGTTTGTTT[-/G]TTTTTTTTTCCCACA | 105670 |
rs226388346 | in-del | -/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73172055 | AAATGATATGGCTTA[-/T]TACAGACTACTTTTG | 105670 |
rs226414980 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144390 | TCACCGTATTGGACA[A/T]TGGCATGCAGGTAAG | 105670 |
rs226447112 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144901 | CTGAACAATGTGTCA[A/G]GGTAGCCCAGGTTGG | 105670 |
rs226504895 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73146585 | TTTTATTGAGGCCTA[A/G]ACTGTTTTCAGCCTT | 105670 |
rs226554265 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73167616 | ATCATGCCGAGCCCT[A/G]ATCTTGAAAGATTTT | 105670 |
rs226555133 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73161028 | TTCGCACACTCGAGA[A/C]TCTTACCCGAGACTC | 105670 |
rs226561085 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144197 | GAACGGAGAGGCGAA[C/T]ATGTTTCTCTTTAGA | 105670 |
rs226648827 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73153269 | AGAGAAGCCTATTGG[A/G]TGAGTCAGGAGGCAC | 105670 |
rs226661467 | in-del | -/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73154417 | GACCAAGGTGTAGAA[-/T]TTTTTTTTTCTCTAT | 105670 |
rs226715210 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141980 | AGAGGGGATCAAGCC[C/T]GCCTCTTCCAAAAAG | 105670 |
rs226788911 | snp | A/G | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141055 | ATCAAAAAATGAAAC[A/G]GGGTTATCTATGATG | 105670 |
rs226825761 | snp | A/G | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141499 | TATTATTGAGTGAAT[A/G]TAGCCACTTACTTTG | 105670 |
rs226846934 | in-del | -/GTCTC | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144131 | TCACTGACCCATCCT[-/GTCTC]GTCTCGGCTTCAGTC | 105670 |
rs226850473 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73167241 | ATATGCATTAAAAGC[C/T]ACAATTTTAACAAAG | 105670 |
rs226885045 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147506 | TACATACTGATACTG[C/T]AAACCCTGCTCTCCT | 105670 |
rs226910422 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73168212 | AGTGTAGAATTGTGG[A/G]AAAGTACTCTTATCA | 105670 |
rs226932153 | snp | G/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152617 | AGGATTCCTAGTCAC[G/T]GATGGAGGTTCCCTT | 105670 |
rs227047896 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73173840 | CCTTCCACACCACAC[C/T]CACTTCTGCTGCACC | 105670 |
rs227068361 | in-del | -/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160000 | AGCAGAAAGTGTGGT[-/C]CCACGAGGACCGCAT | 105670 |
rs227088774 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73149203 | AGTATACAGATCCAT[C/T]GTTACAATTACAAGG | 105670 |
rs227142294 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73143208 | GCCTGCGTGTGGGCG[A/G]CAGGCGCGGGTGGGC | 105670 |
rs227238307 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73182279 | TTGGCCTGGCTGCAT[C/T]GGACTCTTGTGTTAT | 105670 |
rs227253284 | snp | A/C | | | utr-variant-5-prime | Rcbtb2 | Mm_Celera | 14:73138812 | GAATGTCCCGGTGTG[A/C]TCAACTCAGAAGCTA | 105670 |
rs227313675 | in-del | -/ATGTATTC | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73138009 | CATGGGAATGTGTAA[-/ATGTATTC]ATTCAGATGCGTGTG | 105670 |
rs227357081 | in-del | -/C | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141978 | AAAGAGGGGATCAAG[-/C]CCGCCTCTTCCAAAA | 105670 |
rs227478551 | in-del | -/TACA | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137752 | TCTGGGAACTGTCTT[-/TACA]TACTCATTCCATGTC | 105670 |
rs227513453 | snp | A/C | | | synonymous-codon, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73166870 | GGCATCCGTGTCCAG[A/C]GGGTACGTCTCCTGG | 105670 |
rs227582097 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160333 | AAAGGGATTTTTAAG[G/T]CATAGGGAAACTGGA | 105670 |
rs227599557 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163461 | TCATGCAGATCCTTT[C/G]TAGCATGAGTTGCCT | 105670 |
rs227608979 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73180944 | GAACTAAGAGCTCTT[A/G]TTAAAAGGTGGCTGT | 105670 |
rs227626577 | in-del | -/TTT | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73148854 | ACCGATATTCAACAA[-/TTT]TTTTTTTTCCTAGCT | 105670 |
rs227653200 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73173204 | TTTTATGCATTGACC[A/C]AGGTAAGATGATCCA | 105670 |
rs227657532 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73182242 | AGCTTAGGTTCCTCT[C/T]TTGGAGGAAAAGGCT | 105670 |
rs227662660 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165628 | ACACACAAAATGGAA[C/T]TTATAGGCTATGTAG | 105670 |
rs227715984 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73146043 | CCACTGTATTCAGGA[A/G]TCATGTTGTTGAGCC | 105670 |
rs227716337 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73180430 | ATACGCTGAAGCTCT[A/G]GTGAGTCAGGTTGCA | 105670 |
rs227733261 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73171109 | TCAGCCATGCAGTAC[A/G]GCAGGGCCAGAGTGT | 105670 |
rs227736486 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73168962 | TGCATAAATAGAGTG[C/T]TGGCACGTAGGCACT | 105670 |
rs227747697 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73183225 | TTGAGAAAGAAGAAG[C/T]ATCATCTAAAAAATA | 105670 |
rs227762869 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73164873 | TAACCAGCCCAAGCC[A/G]CCGACTTGACTTTCT | 105670 |
rs227788628 | in-del | -/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165089 | AAAGAGGTTTTTGGG[-/T]TTTTTTTTGTTTTTT | 105670 |
rs227842959 | in-del | -/CC | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152163 | CAGAGACAGCTATAA[-/CC]CCCCCCCCACACACA | 105670 |
rs227848880 | in-del | -/A | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179491 | GACTGTTCTGTCCAT[-/A]GGGCCTGGCTGCCCC | 105670 |
rs227865406 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158086 | TAGGAAGCATGCTTG[A/T]AAGGAGAAACAGCTG | 105670 |
rs227990126 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144363 | GTATTCGCACCTTCC[C/T]AGTAAAATCTGTCAC | 105670 |
rs228011067 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163349 | AGAAGACTGAGTAAA[A/G]CCATCCCTGAATTCG | 105670 |
rs228083828 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178127 | CTTTCTTTTTAATTC[C/T]GTGACAACATGTGTG | 105670 |
rs228095488 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73162779 | AAGCCTACACTTTGA[A/G]CTTAGATTCCTGGGC | 105670 |
rs228119775 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169767 | CTCACTTGATGTCCT[A/G]TAAGTTCTCTCTCCC | 105670 |
rs228128694 | snp | C/T | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137043 | CTCAAGCTTGGTTGG[C/T]GTGGCTGGTTGGGTC | 105670 |
rs228186167 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163753 | GCTCCTGCTCTTCCC[C/T]GTCTTGGTCTCTCTG | 105670 |
rs228196363 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144288 | TCACAGTCCTGTGGA[A/G]CTTGGTTCTTTAGTG | 105670 |
rs228295798 | snp | A/G | | | downstream-variant-500B | Rcbtb2 | Mm_Celera | 14:73184470 | GAACATTTAGCTGAA[A/G]TGGACACAAGTGAAA | 105670 |
rs228311867 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159369 | CCGGCAGTACAGACC[A/G]ACAAAGGGAAGAAAG | 105670 |
rs228409191 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141474 | GGCTTAGATATACTC[C/T]TAAGAGGTTTATTAT | 105670 |
rs228414098 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144803 | AATTTGGGGGAGGGG[A/G]ATTATTATTAACAAT | 105670 |
rs228449455 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178912 | ACATGCACCATGGAC[A/G]AGCTCCATACATGTG | 105670 |
rs228480772 | snp | C/T | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137798 | ACTTCAGTACCAAGT[C/T]CAGGAGAGCAAAGTA | 105670 |
rs228683143 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73164220 | AAAGGAAGTCATTTT[A/G]TGGAAGGTGCGCATA | 105670 |
rs228728013 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73182941 | GCTTTGTGGGTAGGT[G/T]GGTGGGGACTGTGTT | 105670 |
rs228740102 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73139471 | CTTTATCTTTTAGAG[C/T]TATTCACTGAAATAT | 105670 |
rs228835021 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73182179 | GTGCTGTGAACAAGC[A/C]TTGAAAGGGGAGGAA | 105670 |
rs228841464 | snp | A/T | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73138630 | CTAGGTACTTGTATT[A/T]CGTGCGTCACCAGGC | 105670 |
rs228891440 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159912 | GCTTCCCGTAGCAGA[C/T]TGGGACTACTGAGTC | 105670 |
rs228946548 | in-del | -/ATT | | | cds-indel | Rcbtb2 | Mm_Celera | 14:73183244 | ATCTAAAAAATAAAC[-/ATT]ATAGTTACCATTTCT | 105670 |
rs229064558 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73140891 | CAAATGTTTTCTCTT[C/T]CCTCCAGCTTTACAT | 105670 |
rs229068731 | in-del | -/TCTACTTTCACGAAGGAAATGGGGGTT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73175901 | TCTCACCACGGAGCC[-/TCTACTTTCACGAAGGAAATGGGGGTT]TAGTTTACTGTGACA | 105670 |
rs229085280 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73180315 | TCTACAGAAGTACCA[C/T]GGGAAAGCCACTTTT | 105670 |
rs229086506 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73173612 | CTTGGGCCTATCCAC[C/T]TCTGTCAGCTAGTTA | 105670 |
rs229121852 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73174120 | CTGAAAGCTGTCTTT[C/T]AGATAAAAAATATAT | 105670 |
rs229180363 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73164237 | GGAAGGTGCGCATAT[C/T]GAGGGCTTTGGGGAA | 105670 |
rs229181232 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179896 | GTATCCACATGGAGT[A/C]GGCTGGCTGGTAGTA | 105670 |
rs229398431 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73164658 | AGCACAGGCCGTGAC[A/G]GCTGCTTACCTTCTT | 105670 |
rs229417641 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73156024 | TAAGTTTACAAACTA[C/T]ATGCTCACCTCCATG | 105670 |
rs229485613 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160482 | GAAGAGCTTTGTTGT[C/T]GCCCTTGTCCTTGTG | 105670 |
rs229506096 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159534 | TATGGTTGCCCATGC[C/T]AATGAGCAAATAAGC | 105670 |
rs229526099 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73162733 | AGAGTGGAATCATTG[C/T]GTGACAACGCTACTT | 105670 |
rs229586921 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160079 | TGAAGTCTAGGGAGC[A/G]TGTGTGACCATGGAC | 105670 |
rs229633132 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73176481 | AGCAGGCTGCATTTG[A/C]AGTCTTGCCGATTAG | 105670 |
rs229649960 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73139603 | AATTTTATTTTCCTG[G/T]TTAATTATTCTATTT | 105670 |
rs229660314 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73157708 | TAATAGTTCCCTCAT[G/T]GATTTAAAAGATGGA | 105670 |
rs229676090 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177213 | TCCAGGCCAGGAGAC[A/G]GACACTGCGATGTTT | 105670 |
rs229820229 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73151987 | TATTAGTCAGGTTCC[C/T]GAAGTATCCTAAACT | 105670 |
rs229838953 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181335 | GTCATGTATACTTTC[C/T]TATGCTGTCTGCTAC | 105670 |
rs229866783 | snp | G/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73157856 | CTAGGAAGGAATGGT[G/T]GTGTCTTATTTTATG | 105670 |
rs229890290 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73150683 | CCCCTCTGTAAGTAT[A/G]CCACTGTCCCTAGGT | 105670 |
rs229966371 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73157381 | GCCCAAGTCTAAGGA[G/T]ACAGGTTCTTGCTTA | 105670 |
rs230057055 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73180318 | ACAGAAGTACCATGG[G/T]AAAGCCACTTTTAAT | 105670 |
rs230083730 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73161821 | AACACACAGCACCAG[A/G]TGTGGGTTACTCCTA | 105670 |
rs230215792 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73173864 | CTGCACCGATGACGT[A/G]TTTGCCTGCTTCGCC | 105670 |
rs230256769 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73174316 | TTCTGGAATGCCCAG[C/T]GAGTAGGGGCCTCCT | 105670 |
rs230262791 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179937 | AGTGAGGTGGCTGTG[C/T]CCACCAGTAGGTGGT | 105670 |
rs230324924 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73180053 | TGGGGATGGGGAAGG[A/C]TAGATTAACGTTCAT | 105670 |
rs230559650 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73161016 | GGTGGAGACAACTTC[A/G]CACACTCGAGACTCT | 105670 |
rs230572072 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178178 | AGATTCTGCTGACCC[A/G]GGAGAGGGGAATTCA | 105670 |
rs230578017 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73170691 | TATGGGTGGGGCAGG[A/G]GGTGAGTCTATAGTT | 105670 |
rs230604126 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177747 | AAACATTAGCAAGTA[A/G]CAGAGTGCCCGGGGT | 105670 |
rs230604846 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73171240 | CCTCCCAGCTAGCTC[A/C]CAGCTGTCTGTCATG | 105670 |
rs230609327 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160526 | TTGGAGATGCTGCTG[A/C]ACAGTTGGATGTATT | 105670 |
rs230614253 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73156395 | AGGAACTAAGGCCTG[C/T]TCATCTCCATGGCCA | 105670 |
rs230641622 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73157323 | ACTAGCTTGCTTCTG[A/G]CTTGCTTCTGGCTTG | 105670 |
rs230646761 | snp | C/G/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73159128 | GGTCCTAGGAGAGAG[C/G/T]GGCATATGGTCATGA | 105670 |
rs230656634 | in-del | -/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165066 | GGCCAAAAGCAACTT[-/G]GGGGAAGAAAGAGGT | 105670 |
rs230674075 | in-del | -/AC | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73171032 | AAAGCAGCAGCAACA[-/AC]ACCCCCCCCCCTTTT | 105670 |
rs230684016 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73183375 | AGGAATGCTGTCATG[C/G]CCACATTTTTAGCCT | 105670 |
rs230688451 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177844 | TTGAATTTGGCACAG[C/T]GAAGCCCATTTATGT | 105670 |
rs230748694 | snp | A/G | | | downstream-variant-500B | Rcbtb2 | Mm_Celera | 14:73184173 | TTCAGATGTCTTATA[A/G]CAAAGTTGACTCTAA | 105670 |
rs230771376 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73146386 | CTGGGTGGCACTTCC[C/T]TTGACAGTGCGCTGG | 105670 |
rs230789300 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73178107 | CCCACTCCCAACCCA[A/G]CCGGCTTTCTTTTTA | 105670 |
rs230838057 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158663 | TAGGGACCTAGCCCA[C/T]ATCACTGCAGCTCCT | 105670 |
rs230839166 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73152708 | ACCTCTCCCTCCTCC[C/T]CTCCTCCCAACTTTT | 105670 |
rs230914848 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73153088 | TAATATAAAGACCCT[A/C]CTTTCCATAACTTGG | 105670 |
rs230914939 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73145827 | TAGATCATTAAACAT[C/T]AGGCTGACACTCGAG | 105670 |
rs231113280 | snp | A/T | | | intron-variant, utr-variant-5-prime | Rcbtb2 | Mm_Celera | 14:73143828 | TTTGCCTTTCTTTAC[A/T]AGGTAAAGATTTAAC | 105670 |
rs231131164 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169907 | TTTGAAAATAGGACC[G/T]TTGACTCCTTAAATG | 105670 |
rs231141702 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181723 | ATATTTTATAAATAG[C/T]TTCAACAACAGAGAC | 105670 |
rs231177043 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73149096 | ACAATGTAGCTAGCT[A/G]AAGATGGCCTTGAAC | 105670 |
rs231178561 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73176254 | AGGGACATAATTCAG[A/G]CAGAATGGAGTAAAG | 105670 |
rs231201720 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159035 | GATATGTATATTTTT[A/T]AAATGTAAAAGTTAA | 105670 |
rs231254209 | snp | A/G | | | intron-variant, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73142928 | AGGGTCGCCGATCCC[A/G]GCCGAGGAGGGAGGC | 105670 |
rs231256237 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73149792 | AAACTGTGAAGTCAT[A/G]TTAACCACATTCTCT | 105670 |
rs231273689 | in-del | -/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169046 | GCTGTAAACATAGTC[-/T]TTTTTATTTTTGAGA | 105670 |
rs231379265 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73176819 | AGACCCCACACTAAG[G/T]TCCCTTCTCTAACCC | 105670 |
rs231425289 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158226 | CTGGTGTACATGCAT[A/G]GGCCTTTGTTCTCCA | 105670 |
rs231447611 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73173484 | TATTTTTAAGACCTA[C/T]TGGTAATCAATAGAT | 105670 |
rs231508697 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73182001 | CTCCTAGTTAAGATT[A/T]TCAAAGGTGAATGTG | 105670 |
rs231546812 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179849 | TTCATTTTTCATTCA[A/G]TATTTAAACAAAACC | 105670 |
rs231699554 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73167069 | ACCCTTTCCTGTAGC[A/G]TCTTGGACAACATAT | 105670 |
rs231700370 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73155001 | GGCAGGGTGGTGCCT[G/T]ACATGCCAATACATA | 105670 |
rs231794017 | in-del | -/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73166659 | AAAGTTGTTTCATAC[-/T]TTTTTAAAACAAAGT | 105670 |
rs231799253 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73172965 | GGCATGCAGGAGGCC[C/T]GGAATCCCTTCAGTA | 105670 |
rs231827887 | in-del | -/GGT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179927 | GGGAATGTCCAGTGA[-/GGT]GGCTGTGTCCACCAG | 105670 |
rs231852968 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73173695 | CCTCCTGTTAATGTG[C/T]CTCTGTGGCATTTGC | 105670 |
rs231908761 | in-del | -/AGTATT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158003 | GAGACTCATGACCTG[-/AGTATT]ATGCAGATCTGTACA | 105670 |
rs231937876 | in-del | -/CC | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73146875 | GCTGCCTCCTCTTCT[-/CC]CTCTCCCTCCCCCTC | 105670 |
rs231961819 | in-del | -/AA | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73161867 | TGACTCTGGAGAAAC[-/AA]GAGTCAAAGACTGTT | 105670 |
rs231983863 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73172606 | GACACTGAAGTTCCC[C/T]GTTTTAATCCTTACA | 105670 |
rs232026706 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73171601 | GAGCTGGTAGACTGC[C/T]ATACTCTCATTTGCT | 105670 |
rs232074745 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73145008 | CACACTAGTGTTAGT[C/T]CTAGGGCTGGCTGGA | 105670 |
rs232091673 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148372 | TAGAAGGTCTTCCTT[C/T]CTCATCTTGGTTTGT | 105670 |
rs232194130 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73154568 | GAACAGGAAAAACCA[C/T]TTGTAGGGCTTAGAG | 105670 |
rs232215732 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73151703 | ACCCAGCAGTAGGAG[C/T]GGGCAGACCAGCTGT | 105670 |
rs232249654 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73156559 | ATGTGAATAGAAAAA[C/T]TCCTACTTCCTTCTG | 105670 |
rs232288829 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73162953 | AATCACGCCTTTGAG[A/G]TGTACATTCCAGGAC | 105670 |
rs232303621 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160024 | ACCGCATTGTACCAC[A/G]GGAACCTAATGGGCT | 105670 |
rs232316684 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163493 | TACGGAAGCCTGGAA[G/T]GATCATCAGAGGCAG | 105670 |
rs232321959 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147624 | TTATGTCCCTAAAGC[C/T]TGGCTTTAGAGCTGA | 105670 |
rs232337948 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73168473 | ACAGTGACTGAACTG[C/T]CACTCGCAGTTCTGT | 105670 |
rs232351129 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73168171 | CCTCAGTCGTCTCTA[A/G]TAATTAAACAGCTCT | 105670 |
rs232355353 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169957 | GAGGCTGATAGTTCA[C/T]TGCTGAACTGGTGTA | 105670 |
rs232390600 | snp | G/T | | | utr-variant-5-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73154389 | TTTGAAACTTTCCAG[G/T]CTCAGAAAAGCTGAC | 105670 |
rs232400584 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152084 | ACTCTAAATGTCAGC[A/G]TTCCACACACCAGGC | 105670 |
rs232405468 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163904 | AACACATGAGACCTG[A/G]TAGAAGTAGTGGACA | 105670 |
rs232415054 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73170499 | TGTCCTTCTGAGCTT[A/G]CACAGCGTCAGGCAG | 105670 |
rs232453954 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73174631 | CCTGCTGTTGTGGGT[A/G]TATGTCACACTAAAT | 105670 |
rs232454325 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73175183 | GCCTTGCAGACAGTC[C/T]TGAACACAGCACTGC | 105670 |
rs232476984 | snp | G/T | | | utr-variant-5-prime | Rcbtb2 | Mm_Celera | 14:73138866 | GAATTACCATGTGAG[G/T]AGAAATCGGGGATCT | 105670 |
rs232609219 | snp | C/G | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73138073 | AGTAAGCCCCGGGGA[C/G]CTTTCTCTACTACTC | 105670 |
rs232611169 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73145727 | CAGGTGACTCTTCTC[C/G]CTTCCCTTATCTGGA | 105670 |
rs232612638 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73149444 | TTTAGAGGTTTATTT[C/T]TAAGTGTGTGTATGT | 105670 |
rs232645213 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160208 | AACCTTGCACCGTTC[A/C]AGGAAAAAGACAAAG | 105670 |
rs232678172 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160624 | AGATGAACCTGCTTA[G/T]CACCATAATGGGCAT | 105670 |
rs232681407 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152207 | CTCACACACTGCATC[C/T]CAAATGGTGCAAATT | 105670 |
rs232775915 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73156887 | GTCTCTAATTCATGG[C/T]AGGTGAATTTCTGGT | 105670 |
rs232798975 | in-del | -/AA | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73151414 | GCTATTTTTTAATAC[-/AA]GACATGATACAATTT | 105670 |
rs232828327 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73150576 | AAATAAATAAATAAA[C/T]AAATAAACAAACAAA | 105670 |
rs232887264 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147421 | CTAATAAAAGGAAAT[A/G]ATACTGTTTGATTAC | 105670 |
rs232899761 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73140650 | CTACAATACTCAGAG[C/T]CCAACCTGCCTGTTG | 105670 |
rs232919037 | snp | A/G | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73140871 | GCCCTTTTGGGGGAG[A/G]GGTTCAAATGTTTTC | 105670 |
rs232961300 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73150761 | TGTGATGAATATGAG[C/T]ATCTTTAGCCCCTTG | 105670 |
rs232968455 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73146559 | ACACTGAAGCTTCTA[A/G]CTCCATACAATTTTA | 105670 |
rs233013325 | in-del | -/TGCTGAGCTG | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163159 | TACCTGCCTAGCTGA[-/TGCTGAGCTG]TGGTTTGTACGCTTG | 105670 |
rs233045012 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147145 | ATGTCTGCATTCCAG[C/G]CACAGGGATTAAACA | 105670 |
rs233045441 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73140112 | TTTCCATGCCAGGAA[A/C]GTCCTGACCGTGAGA | 105670 |
rs233054890 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73176081 | GCAATCTTCCTCTTT[C/G]TGAGGCATGACACGT | 105670 |
rs233098653 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73168842 | GACACATAAACATCA[C/T]ACTACTTCCCCTATA | 105670 |
rs233196244 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73164610 | GATTCCATCGATGGC[A/G]ATCCAGGCACGGGTT | 105670 |
rs233270988 | snp | C/T | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137371 | CATTCATCAGGTGAA[C/T]GGGTGGATTTATCTA | 105670 |
rs233272578 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73150270 | TTTTGGGCACTAGGC[C/T]AATGTATGTTTCAAA | 105670 |
rs233281686 | in-del | -/A | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73171034 | AGCAGCAGCAACAAC[-/A]CCCCCCCCCTTTTAT | 105670 |
rs233318031 | in-del | -/CG | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73153473 | TGCAAATGGTCTGCC[-/CG]CGAATTTCACCTTCA | 105670 |
rs233335612 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177157 | TCAGAGACCTTACCA[A/C]CAAGTTGGCAAATGT | 105670 |
rs233341140 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144072 | AAATCGTGAGCAAGG[C/G]GTGTATGTGCAGAGT | 105670 |
rs233359937 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73155681 | CCAGTATCCAGTGAT[A/G]CTGTTTCCCACCCAG | 105670 |
rs233367019 | in-del | -/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73151771 | CTCGCTCGAAGACAC[-/T]TTAAGTTACAAAAAT | 105670 |
rs233372083 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169829 | CTCTGAGTCCTGGGA[A/G]TAACATGGTCAATCT | 105670 |
rs233518370 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73156323 | TGCTCTTGCCGAGGA[A/C]AAGAGTTTTTGGTTC | 105670 |
rs233679022 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73161577 | CCGGGAAGGGCTATG[C/T]GTAGTTCTACAGCTG | 105670 |
rs233683776 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73171720 | TGCCTCAGTCTTTGG[G/T]ACTACCTCATTTCAT | 105670 |
rs233814845 | snp | A/C | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73145402 | AAAACTATTATTCTT[A/C]CGGTATACCTGCAGG | 105670 |
rs233815092 | snp | A/G | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73142203 | CCCCTAAACTGATGT[A/G]TGTGTATATATATAT | 105670 |
rs233847541 | snp | A/C | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73150433 | AGGTTGGAGCCTTCA[A/C]AACCTAGTTGCCTCC | 105670 |
rs233890452 | in-del | -/A | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73145384 | CCATGCTCAGGCACG[-/A]AAAAAACTATTATTC | 105670 |
rs233897680 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73146960 | TGAGTTGGGTGTATT[A/C]TGTCTCTGACTCATT | 105670 |
rs233927067 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148734 | AATATGGATATCCAC[G/T]TCTGCTCTGGTCCTT | 105670 |
rs233958088 | in-del | -/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73166883 | GCGGGTACGTCTCCT[-/G]GGGGGGCGGGGGGCG | 105670 |
rs234129594 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73183431 | GGCACTCAGTTAATT[C/T]ACTGTCCATCATAAG | 105670 |
rs234131614 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177420 | TCGATCACCACTGGA[A/G]CATCACAGGCAAGCA | 105670 |
rs234173194 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73183758 | CTTTATATTGAGGGT[C/T]TCTCTATATAAGATT | 105670 |
rs234217198 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73172413 | AGCTGTGCAGCGATG[A/G]GTTAACCAAACTGCC | 105670 |
rs234223925 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177801 | ACACTCTGGGTGAGT[A/G]TTGAATAAGAGGACT | 105670 |
rs234230657 | in-del | -/AAAC | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73150576 | AATAAATAAATAAAT[-/AAAC]AAATAAACAAACAAA | 105670 |
rs234254296 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73166187 | TGTATGTAGTAAGGA[C/T]TTCAATCACTACAAA | 105670 |
rs234275983 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73170311 | AAGCAATGAAGGGGA[A/G]GATGGGGTGCCCGTA | 105670 |
rs234298858 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73182770 | GTCTTCTGTCAAAAG[A/G]CTGTAGTCAGTTCTC | 105670 |
rs234362662 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73164258 | CTTTGGGGAAACACG[C/T]TATGTTTTGGCCTGA | 105670 |
rs234401568 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181279 | TGTGGGTGGGCATCC[C/T]TCCAACATTCTGTAG | 105670 |
rs234411363 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177551 | TCGGCTGTGAAAGTG[G/T]GCATTTTAGGTAACT | 105670 |
rs234418500 | snp | C/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73155774 | GATGCTGTTTCCCAT[C/G]CAGTATCCAGTGGAT | 105670 |
rs234440320 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73145525 | TTGCTGTTTTCAAAG[C/T]TTATCTGATTTGATT | 105670 |
rs234490236 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181756 | AATTTTAAACTTTGA[A/G]TATGAACAGGTGGTG | 105670 |
rs234522803 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163795 | GCGTAGCCTTGCTTG[C/T]TCATGTGGAAAAGGA | 105670 |
rs234524484 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158176 | TCTGTGAGCGTGGTG[C/T]ACTGGGCCCTGAGGG | 105670 |
rs234537586 | in-del | -/GA | | | utr-variant-5-prime | Rcbtb2 | Mm_Celera | 14:73138888 | CGGGGATCTCTGAAG[-/GA]GAGATTCCCAACATT | 105670 |
rs234565814 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158732 | GTGAGGTTTATTTTT[G/T]CATGCCCACTGATAC | 105670 |
rs234566634 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73180610 | GGCCGGCTGAGATAA[C/T]CAATGCATGTTTGTG | 105670 |
rs234571207 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144557 | CACAGTGGCAGTGCT[A/G]TAGGACTCAGGATGG | 105670 |
rs234607550 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163009 | CCGATTATTCAGACC[A/G]TTTCTTAGTTAAAAA | 105670 |
rs234614653 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73162698 | GGCTGCAAGACGATG[C/T]ACAAAGCCCTTCTGT | 105670 |
rs234650274 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163603 | ACATCCTTGTGGCCT[G/T]TCCTTGCTGATTTAG | 105670 |
rs234718746 | snp | A/G | | | upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73137987 | TGTGTGTGGGGGACC[A/G]AGTATGCATGGGAAT | 105670 |
rs234741342 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73162141 | TATGTTTAGTAATGG[A/G]TTTGTAAATTGAAGA | 105670 |
rs234843918 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73166996 | TAAGGTGCAGATCTT[C/T]AGGGAGATGCTGTGT | 105670 |
rs234849535 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73167891 | TTATGGGCAGGCTGC[A/C]TGCCCTTGGTTTTCA | 105670 |
rs234880906 | in-del | -/TT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177611 | TATATAGGTAATAGA[-/TT]TTTTTTTTTTCATTT | 105670 |
rs234885351 | snp | A/C | | | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | Rcbtb2 | Mm_Celera | 14:73162419 | GGATTCTCTAACTGG[A/C]AAAAAAATAGCCAGC | 105670 |
rs234987594 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73156368 | CACAATCGTCTATAA[C/T]TCCAGCTTCAGAGGA | 105670 |
rs235003129 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73142684 | TTCCTTCATTTTAAA[A/G]TCGGACAGCTCTCTG | 105670 |
rs235044819 | snp | A/G | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141666 | GGTATTTGTTGTTGG[A/G]TCCTATTTGATGACA | 105670 |
rs235045989 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73142412 | TTCTCTTAGGACTTT[C/T]TAGTGCACACTGCTC | 105670 |
rs235078041 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160646 | AATGGGCATCACAGG[C/T]AAAACAAGGCCCATA | 105670 |
rs235186021 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160165 | GTCAATATGAGCCCA[G/T]TGAACAGAGATTCTA | 105670 |
rs235216682 | snp | A/C | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141893 | CAGCCCATTGTTATA[A/C]TAAGTTCACAGACTG | 105670 |
rs235233123 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148103 | TCCTTTTGTTTACCA[G/T]TCTTCAGCTTTGCTG | 105670 |
rs235241271 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73179973 | TAGCCCCACCCAGGT[C/T]GTTGGCTATAGGAAT | 105670 |
rs235266393 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159277 | AAGATGAGGTCATAA[A/G]GGTTGGTACTAATCC | 105670 |
rs235300375 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165736 | TGTCTCAGCTGGGCT[C/T]CAGTATACACTGGAA | 105670 |
rs235452192 | in-del | -/GAGGCG | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73171888 | AGCACTTGGGAGGCA[-/GAGGCG]GAGGCGGAGGCAGAG | 105670 |
rs235468883 | snp | A/C | | | intron-variant, upstream-variant-2KB | Rcbtb2 | Mm_Celera | 14:73140500 | ATCTGGGGTCCCAAT[A/C]CTGCTGGTCTTCTTG | 105670 |
rs235554417 | snp | A/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159182 | TGATCCCCCAAGACT[A/C]TGATCCAAAGTCCAA | 105670 |
rs235555227 | snp | A/G | | | utr-variant-5-prime | Rcbtb2 | Mm_Celera | 14:73138917 | ATTTACTGAGTGCAT[A/G]GATGTAGGCACTGAG | 105670 |
rs235645912 | in-del | -/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152286 | AACAAGTCTACCATC[-/T]TTTTTTCAAACAATA | 105670 |
rs235720340 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165671 | CAACAAAGACTGTTT[A/T]CCAATGAAAGGTCCA | 105670 |
rs235808434 | in-del | -/CTTCAG | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181612 | TTTTTCTGCATTCAT[-/CTTCAG]CATTTGCTAGAGTTT | 105670 |
rs235908531 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73180545 | GGGGGAGCCAGAAAC[A/G]GCTTTTCCTGGTAAT | 105670 |
rs235936101 | snp | A/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73145097 | TGAACATTGACAGAG[A/T]ATAGACTTGCTGGGG | 105670 |
rs235968437 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181787 | GTACCTTTGTGCTGA[A/G]TCAGACCATACCTGG | 105670 |
rs236113962 | snp | C/T | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73156432 | TGTCTGTCTTCTCTC[C/T]CCCTCTCCCCACCCT | 105670 |
rs236224330 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73161217 | ACAAAGGGAAGAAAT[C/G]TTACATTGGGTTGCA | 105670 |
rs236238539 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73173241 | TATCTAGTTAGTAAT[A/G]CTTTTAAGGGTTAAA | 105670 |
rs236255071 | in-del | -/CG | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165579 | TATCTTATCATCGCA[-/CG]CACACATACACACAC | 105670 |
rs236339081 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141796 | TTTTGGGCCCATAAA[C/T]TATTACGTGACACAC | 105670 |
rs236351280 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73162896 | AGAAGTTTGCCTTAG[C/T]AGTGGAGCGAGAACA | 105670 |
rs236354721 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179344 | TAGCCTCCCTCCCCA[C/T]TGACTTTAAAAAATA | 105670 |
rs236366179 | in-del | -/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177397 | GTAGCTCTAGTAAGA[-/G]GTCAACATCGATCAC | 105670 |
rs236504102 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73179219 | CTTCCTGAACTTTCT[A/G]CAGTGGCTGTGAATT | 105670 |
rs236514702 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73168496 | AGTTCTGTGGCTGTC[A/T]TGTAAGTGCTTTCTC | 105670 |
rs236544128 | in-del | -/A | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163322 | CTTGGTGAATTCTAG[-/A]GAAGGAAAAGGAGAA | 105670 |
rs236644381 | in-del | -/A | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73144700 | AAAAACTACGTAGCC[-/A]ACTTTCCGTATCCTT | 105670 |
rs236654186 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73170169 | CTGCACTCACCTTAG[C/T]ATCTCCAAATAGACT | 105670 |
rs236681693 | in-del | -/AATC | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152227 | GGTGCAAATTAGGGA[-/AATC]AATCAGTTTTCTCTG | 105670 |
rs236690663 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73154503 | AGGACCTCTGTTTCT[A/G]CAGGGTGACCTCTCC | 105670 |
rs236729473 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73176710 | ATATCTTGGTGGGAA[C/G]TGCCTACTGGAACCA | 105670 |
rs236759303 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159687 | TCCACCTTGACTGGG[C/T]GGCACCTTCAGGTAA | 105670 |
rs236775334 | snp | C/T | | | intron-variant, utr-variant-5-prime | Rcbtb2 | Mm_Celera | 14:73143609 | AGCCGCCTCGCCGAC[C/T]CCATGGCGGCACACG | 105670 |
rs236802440 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73153904 | GTCCTGGAACTCACT[C/T]TGTAGACCAGGCTGG | 105670 |
rs236818672 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177481 | TGTGAATGCAGAGCC[C/T]TAGAAGATCTCTTTG | 105670 |
rs236820324 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73169777 | GTCCTGTAAGTTCTC[G/T]CTCCCTACTGTCAGG | 105670 |
rs236825532 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73181816 | GGGTGTAGAACACTC[C/T]CTTAGAAAGCCTACT | 105670 |
rs236912105 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73176521 | AAGCAAGGAGCCAAG[A/G]CAATGACAAGGTTTT | 105670 |
rs236970762 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165169 | AAGTCAGGGAAGAAA[C/T]TCAAGACAGGAACCT | 105670 |
rs236991181 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73152098 | CGTTCCACACACCAG[A/G]CTTATGTTTTACAGG | 105670 |
rs237019025 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73159718 | CAGGCCAGATAAAAA[G/T]CTATTTCAGAAGGAT | 105670 |
rs237026215 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73180735 | AGGAGGTAGGCCTTA[G/T]ATTAATCATGGACCA | 105670 |
rs237073398 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73157972 | CCTCATTCACACAGA[A/G]GAATCTTCCTGTTCA | 105670 |
rs237105923 | snp | G/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73151210 | TTCGATTTACATGGT[G/T]AATTTCAGGTCAGTC | 105670 |
rs237110390 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158305 | CTAGAGAGAATATAT[A/T]AAAACCACAGAAGGC | 105670 |
rs237119403 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73175020 | GCAGACAGCCCTGCA[C/G]ACAGCCCTGAACACA | 105670 |
rs237125844 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73150190 | GTTCAAGTCCCAGCA[C/T]CCACATGGCTGCCCA | 105670 |
rs237188833 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73180316 | CTACAGAAGTACCAT[A/G]GGAAAGCCACTTTTA | 105670 |
rs237199742 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73140076 | TTATAAACAACGCTG[C/T]AGTGATGATCCTTTG | 105670 |
rs237203225 | in-del | -/ATGT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73177769 | GCCCGGGGTCAGAGC[-/ATGT]ATGTCCCCACAGTAC | 105670 |
rs237208596 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73157891 | TAATTCAGTAATTCG[A/G]TCTTACCTGACATTT | 105670 |
rs237224142 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73173941 | TTTCCCTCTTGGGAC[A/G]GTTCTGAGAACGAGG | 105670 |
rs237236110 | snp | A/G | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141940 | GAACTTTCAGCCTCA[A/G]GAACCGTGAACTTGC | 105670 |
rs237281607 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73149236 | TCTTTTAACTTTGGC[A/G]TCACCTTCATCAAAA | 105670 |
rs237370673 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | Rcbtb2 | Mm_Celera | 14:73183645 | TCTACTTTCTGCATT[A/C]ACTTCTCATAATGGC | 105670 |
rs237371052 | in-del | -/ATCAATCA | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73165551 | TTCATCTATCTATCT[-/ATCAATCA]ATCATCTATCTTATC | 105670 |
rs237384065 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73156059 | AGTTTAATATAGTCA[C/T]TTGTTATTTTTCTAC | 105670 |
rs237432651 | snp | C/T | | | upstream-variant-2KB, intron-variant | Rcbtb2 | Mm_Celera | 14:73141484 | TACTCTTAAGAGGTT[C/T]ATTATTGAGTGAATA | 105670 |
rs237435634 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73148611 | GAGCTGGAGGATGAA[A/G]AAGCAGTGAAATTCC | 105670 |
rs237484782 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158778 | TCTGGTGTTTAGTAA[C/T]TGAAGAAACAGTAAT | 105670 |
rs237547673 | snp | C/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73156306 | CAATGAGGAGTGCCT[C/G]TTGCTCTTGCCGAGG | 105670 |
rs237557349 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73163821 | AAGGAGCATGCGTGA[A/G]CACTGCCACACTTGG | 105670 |
rs237568071 | snp | A/G | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73155345 | GCTGTTTCCCATGCA[A/G]TATCCAGTGATGCTG | 105670 |
rs237584461 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73147922 | TGCTCCATCATCACC[C/T]TAACTCCTCTGTGTG | 105670 |
rs237625907 | in-del | -/AT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73154669 | TTAATGAGAAGTAAC[-/AT]AACTTTGTTTGTCTG | 105670 |
rs237727946 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73157197 | AGTTAAGGAGAAAGG[C/T]GTTTATTTTTGCGTA | 105670 |
rs237753258 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73146816 | GTCTTGTTCTCTCTT[C/T]GCCTATTGCTTGTTC | 105670 |
rs237855975 | in-del | -/C | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73152754 | TCATTCCCTTCCCTG[-/C]CCCTTCCATCTTATT | 105670 |
rs237868861 | snp | C/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73153347 | GATCTGCTGAAGTGC[C/T]ATAATATATAATGGT | 105670 |
rs238007645 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73153810 | AAGCCTAATACATTA[A/G]AAAACAGTGGCCATT | 105670 |
rs238009455 | snp | A/G | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73158985 | TACAAACCTTCATTC[A/G]AGGCACCAATGGAGT | 105670 |
rs238012249 | in-del | -/CCTGTGTAGT | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73173319 | GTTTCTCTGTGTAGC[-/CCTGTGTAGT]CCTGAAACTCACTCT | 105670 |
rs238036569 | snp | A/T | | | intron-variant | Rcbtb2 | Mm_Celera | 14:73160691 | AGTTTGGGTTTCAGT[A/T]GCTGCAGCCAAGCAC | 105670 |
rs238378449 | in-del | -/TACA/TACACA/TACACACA/TACACACACA/TACACACACACA/TACACACACACACA | | | intron-variant | Rcbtb2 | GRCm38.p3 | 14:73152167 | ACAGCTATAACCCCC[lengthTooLong]CCCCCACACACACAC | 105670 |