SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6175057 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | Ccdc12, Nbeal2 | GRCm38.p3 | 9:110655500 | gtgccgggattaaag[G/T]cgtgcgccaccacgc | 235627 |
rs6189046 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Ccdc12, Nbeal2 | GRCm38.p3 | 9:110655778 | ATTTGCTTTTAAGCA[A/G]GTAAGGTAGCCTGAC | 235627 |
rs29593654 | snp | A/G | 0.444444 | 0.157135 | intron-variant, downstream-variant-500B | Nbeal2, Mir8107 | Mm_Celera | 9:110635748 | AGAAAGCTTCTTCAC[A/G]CCCTCCAGGGCAGGG | 235627 |
rs29595119 | snp | C/G | 0.32 | 0.24 | intron-variant | Nbeal2 | GRCm38.p3 | 9:110652146 | GGAGGGGCCACCTGC[C/G]CTGCTGGCTGGTTGG | 235627 |
rs29843569 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nbeal2 | Mm_Celera | 9:110651116 | TGTGTGTGTGTGTGC[A/G]CGTGCGTGCACTGCT | 235627 |
rs29890894 | snp | A/C/G | 0.32 | 0.24 | intron-variant | Nbeal2 | GRCm38.p3 | 9:110649429 | AGCTCCAGTCTGTCC[A/C/G]GGCATTTTAGGACAA | 235627 |
rs29986349 | snp | A/G | 0.375 | 0.216506 | stop-gained | Nbeal2 | Mm_Celera | 9:110641482 | GGGGCGCCCGGGCCT[A/G]CAGGTAAAGCTGTGG | 235627 |
rs30042960 | snp | A/C | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Nbeal2, Mir8107 | GRCm38.p3 | 9:110638061 | ATGCTCTCACCCCAC[A/C]CTGGGCCACATGAGA | 235627 |
rs30126001 | snp | A/G | 0.415225 | 0.187619 | synonymous-codon, downstream-variant-500B | Nbeal2, Mir8107 | GRCm38.p3 | 9:110635946 | GAGGAGGGGCCCACC[A/G]CCATCAGCAGCCGCC | 235627 |
rs30179325 | snp | A/T | 0.375 | 0.216506 | upstream-variant-2KB | Ccdc12, Nbeal2 | Mm_Celera | 9:110655996 | TGACCTCAGAGTGAG[A/T]TGGGAATGAGAGTGG | 235627 |
rs30374967 | snp | G/T | 0.277778 | 0.248452 | synonymous-codon | Nbeal2 | Mm_Celera | 9:110638628 | GGGCCGTAGTGACAC[G/T]CGACCCAGAGCTTGC | 235627 |
rs33289864 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nbeal2 | Mm_Celera | 9:110631167 | ATGGGCCAGCAAAAC[A/G]TTACAGAGCCCCCAC | 235627 |
rs33289865 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Nbeal2 | GRCm38.p3 | 9:110632205 | CCTGGGCATGCAGCT[A/G]TAGGTGCAAGGCAAT | 235627 |
rs33289866 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Nbeal2 | Mm_Celera | 9:110632365 | CCGGAGATCTGCTGT[A/G]CTATTGGCGAGATGT | 235627 |
rs33289868 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Nbeal2 | Mm_Celera | 9:110632547 | CAAGGTCACTCACTG[A/T]AAGGTATACCCAGCC | 235627 |
rs33289870 | snp | C/T | 0.32 | 0.24 | intron-variant | Nbeal2 | GRCm38.p3 | 9:110632589 | CTGCCATCCATTGAA[C/T]GCTTGGCCTGACTAA | 235627 |
rs33289872 | snp | C/T | 0.244898 | 0.249948 | synonymous-codon | Nbeal2 | GRCm38.p3 | 9:110633057 | GAAGACCTGGCCACG[C/T]TCCCGCCAGGCGGCC | 235627 |
rs33290904 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Nbeal2 | GRCm38.p3 | 9:110633260 | AAGAGAGGCAGCATT[C/T]GGCAAACAGCCAGAC | 235627 |
rs33290906 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nbeal2 | Mm_Celera | 9:110633375 | CAGAGAGGAGATATT[C/T]ACAAAGGCCTTACTC | 235627 |
rs33290908 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nbeal2 | Mm_Celera | 9:110633507 | TCCTATCTGTAGGCC[C/T]TACAAAGCCTGGGCC | 235627 |
rs33290910 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nbeal2 | Mm_Celera | 9:110633580 | CGTGACAGTACCAGC[C/T]CTGGTATTAGACCGC | 235627 |
rs33290912 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nbeal2 | Mm_Celera | 9:110633620 | AAGACCACACTGCCA[A/G]CTCTCCATTCCTGAG | 235627 |
rs33291794 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Nbeal2 | Mm_Celera | 9:110633754 | GCCATCTTCCAGCAC[A/G]TTGGAGAGACTGGAG | 235627 |
rs33291796 | snp | G/T | 0.391111 | 0.206368 | synonymous-codon | Nbeal2 | Mm_Celera | 9:110633877 | GCTGCCGCCACCAGC[G/T]GTATTGCCCGAGCCA | 235627 |
rs33291798 | snp | A/G | 0.32 | 0.24 | intron-variant | Nbeal2 | GRCm38.p3 | 9:110634216 | CCAAACCAGGGGACA[A/G]CAAATAAGAGGTCAT | 235627 |
rs33291800 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nbeal2 | Mm_Celera | 9:110634954 | TGTGTGGCTCCAGAA[A/G]AGGCCTGTGAAAGTG | 235627 |
rs33291802 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nbeal2 | Mm_Celera | 9:110635003 | CTTCTAGCCGGCGGC[C/T]TCAGTAAATGGGATT | 235627 |
rs33292544 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Nbeal2 | Mm_Celera | 9:110635157 | CAAGGGGTCTTGCAC[C/T]GGAGAACCCTGAAGC | 235627 |
rs33292546 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Nbeal2 | GRCm38.p3 | 9:110635307 | GCCTACCTGGCCATC[A/G]TCACCGGTAGCTGCC | 235627 |
rs33292548 | snp | A/C | 0.231111 | 0.249285 | intron-variant, downstream-variant-500B | Nbeal2, Mir8107 | GRCm38.p3 | 9:110635611 | AGGGCCCGCCAGCCT[A/C]ACCTGTAGTGCGTGC | 235627 |
rs33292550 | snp | A/G | 0.408163 | 0.193609 | synonymous-codon, downstream-variant-500B | Nbeal2, Mir8107 | GRCm38.p3 | 9:110635943 | GTAGAGGAGGGGCCC[A/G]CCGCCATCAGCAGCC | 235627 |
rs33292553 | snp | A/T | 0.231111 | 0.249285 | missense, nc-transcript-variant | Nbeal2, Mir8107 | GRCm38.p3 | 9:110636011 | TCATATCCATGGCCG[A/T]ACTGGGGACCTGAGG | 235627 |
rs33293385 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Nbeal2, Mir8107 | GRCm38.p3 | 9:110636133 | CTGCTCACAGCTTTT[C/T]AGGGCCGCTGCCATC | 235627 |
rs33293387 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Nbeal2, Mir8107 | Mm_Celera | 9:110636473 | GGTCAAGGGTGTGCC[A/G]GAAGCCACTACCTCA | 235627 |
rs33293388 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Nbeal2, Mir8107 | Mm_Celera | 9:110636810 | AGCCTGGACTCTCTC[A/G]AACTGGTCTCCCAAA | 235627 |
rs33293389 | snp | A/G | 0.231111 | 0.249285 | missense, upstream-variant-2KB | Nbeal2, Mir8107 | GRCm38.p3 | 9:110637103 | TGGAGGAGCAACTTG[A/G]TGCCAAACTCATGTA | 235627 |
rs33293391 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon, upstream-variant-2KB | Nbeal2, Mir8107 | Mm_Celera | 9:110637117 | GGTGCCAAACTCATG[C/T]AGTTCACCCTCAGGC | 235627 |
rs33293392 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, upstream-variant-2KB | Nbeal2, Mir8107 | Mm_Celera | 9:110637623 | GACTGATGACGCGGG[A/G]AGCCCTGTGGTGGTT | 235627 |
rs33293914 | snp | C/T | 0.124444 | 0.216185 | missense | Nbeal2 | Mm_Celera | 9:110642402 | TTCCTCCTGCAAGGA[C/T]GGCACCAAAGAGGTG | 235627 |
rs33293915 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nbeal2 | Mm_Celera | 9:110642540 | AAGGACTGCACAAGA[A/G]GTGGGATATCCCAGC | 235627 |
rs33293916 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nbeal2 | Mm_Celera | 9:110642600 | GTACGCTAGAGGGAT[G/T]TCAGTGGTGCTTGAG | 235627 |
rs33293917 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nbeal2 | GRCm38.p3 | 9:110642667 | CCTAGATCCTTATGT[C/T]CAAAAAGGAGGGCTT | 235627 |
rs33293918 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nbeal2 | Mm_Celera | 9:110642792 | GTGGGAGTTCCTGGC[A/G]CTCTGACCTGGGGAC | 235627 |
rs33293919 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nbeal2 | Mm_Celera | 9:110643001 | ATGAGCATCAGTCCT[A/G]AGGATGTCAGGCTAC | 235627 |
rs33293920 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Nbeal2 | Mm_Celera | 9:110643063 | AATCTAGATGGTTCT[A/G]GGAGTGCCTAGGCTG | 235627 |
rs33293922 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nbeal2 | Mm_Celera | 9:110643322 | GCCAGGGAGAACAAA[C/T]GGCCAGAAGGGCTTC | 235627 |
rs33294404 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Nbeal2, Mir8107 | GRCm38.p3 | 9:110637800 | AGAGCAGTACAGGCT[A/G]AAGATACACAGGGTT | 235627 |
rs33294405 | snp | A/G | 0.473373 | 0.11227 | synonymous-codon | Nbeal2 | GRCm38.p3 | 9:110638119 | CGCGAAGGACACTTC[A/G]GGCAAGTTCACGGTC | 235627 |
rs33294407 | snp | C/T | 0.142012 | 0.225474 | missense | Nbeal2 | GRCm38.p3 | 9:110638126 | GACACTTCGGGCAAG[C/T]TCACGGTCACGTACT | 235627 |
rs33294409 | snp | C/T | 0.132653 | 0.220748 | missense | Nbeal2 | GRCm38.p3 | 9:110638130 | CTTCGGGCAAGTTCA[C/T]GGTCACGTACTCCTT | 235627 |
rs33294411 | snp | A/G | 0.124444 | 0.216185 | missense | Nbeal2 | Mm_Celera | 9:110638537 | CGGCGCCTGCATGGC[A/G]AGCCTTCTGAGATTC | 235627 |
rs33295074 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nbeal2 | Mm_Celera | 9:110643357 | CTTCACTCCTCCAGG[A/G]ATACGGAAGCAGAGG | 235627 |
rs33295076 | snp | A/T | 0.124444 | 0.216185 | synonymous-codon | Nbeal2 | Mm_Celera | 9:110644491 | CAGCTGCTCCGCTAG[A/T]GCATGTAGAGCATCT | 235627 |
rs33295078 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Nbeal2 | GRCm38.p3 | 9:110644900 | AACCAGAGGACTGTG[G/T]TGTGGACAGGTCACC | 235627 |
rs33295080 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Nbeal2 | GRCm38.p3 | 9:110644978 | CAGAGACCTGACACA[A/G]GCAGAGGAGGAGCTT | 235627 |
rs33295082 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Nbeal2 | Mm_Celera | 9:110645592 | TTCAAAGTACCCACA[A/T]TTCCTGACGTGGCTT | 235627 |
rs33295454 | snp | A/C | 0.142012 | 0.225474 | synonymous-codon | Nbeal2 | Mm_Celera | 9:110638655 | TTGCAGCAAGGCTAA[A/C]AGCTGCTCCTGGCAG | 235627 |
rs33295456 | snp | A/G | 0.32 | 0.24 | synonymous-codon | Nbeal2 | GRCm38.p3 | 9:110638748 | CACACAGGTGGTGCG[A/G]CTGGCAGGGCAGCTG | 235627 |
rs33295458 | snp | G/T | 0.165289 | 0.235211 | synonymous-codon | Nbeal2 | Mm_Celera | 9:110638823 | AGCTGTGGGCAGTGC[G/T]GGTAGCCACTGCATC | 235627 |
rs33295460 | snp | C/T | 0.32 | 0.24 | intron-variant | Nbeal2 | GRCm38.p3 | 9:110638923 | TGTAGGTGGAAAGAA[C/T]GTGACAATCCCGGTC | 235627 |
rs33295462 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nbeal2 | GRCm38.p3 | 9:110639089 | TCCATGCTTTTGGCT[C/T]GTAGCCTAGTATGGC | 235627 |
rs33295794 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nbeal2 | Mm_Celera | 9:110646711 | CCTGCACGGTTACCC[G/T]GAAGGCAATGCAAAG | 235627 |
rs33295796 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nbeal2 | GRCm38.p3 | 9:110646997 | ATTATCCATTGATAG[A/G]TTTGTGATCTGGGCT | 235627 |
rs33295798 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nbeal2 | GRCm38.p3 | 9:110647359 | AACCCGCTACGGGAC[A/G]TGGAAAGCCTCAGAA | 235627 |
rs33295800 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Nbeal2 | GRCm38.p3 | 9:110647821 | GATCCCGGATCTGTG[C/T]TTCTCAGAATCTGGG | 235627 |
rs33295802 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Nbeal2 | Mm_Celera | 9:110648444 | CTCTGAAGGGGACTC[G/T]AAGGACAGACGAGGA | 235627 |
rs33296334 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Nbeal2 | Mm_Celera | 9:110639437 | TATGGGTGCTGTGGG[A/C]AACTTGCACTCCCTT | 235627 |
rs33296336 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nbeal2 | Mm_Celera | 9:110639502 | GTCACAGTGCAGAAA[A/G]AACAAGGACAACAGA | 235627 |
rs33296338 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nbeal2 | Mm_Celera | 9:110639588 | GTGTCCTTTCTCTAC[A/G]TGGCCGGGACCCAGG | 235627 |
rs33296340 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nbeal2 | GRCm38.p3 | 9:110639599 | CTACATGGCCGGGAC[C/T]CAGGACACCCAACTC | 235627 |
rs33296342 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nbeal2 | Mm_Celera | 9:110639651 | ACCCACCAAGCCTAT[C/T]GAACCACACCCCAGC | 235627 |
rs33296520 | snp | C/T | 0.32 | 0.24 | missense | Nbeal2 | Mm_Celera | 9:110626573 | ATGCACGTGGTATCC[C/T]GGGAGCCGGAGATGA | 235627 |
rs33296522 | snp | C/T | 0.197531 | 0.244432 | synonymous-codon | Nbeal2 | GRCm38.p3 | 9:110629857 | TAGGCGCAGAAGCAA[C/T]GAGTACACCTGGTTC | 235627 |
rs33296523 | snp | C/T | 0.21875 | 0.248039 | synonymous-codon | Nbeal2 | GRCm38.p3 | 9:110630007 | GAAGAAGAGTTCGAG[C/T]GCCGAACGCCGCAGG | 235627 |
rs33296704 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nbeal2 | Mm_Celera | 9:110648516 | AGGAGGAAGTACTTG[A/G]ACCTTGCTACAGGGG | 235627 |
rs33296706 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nbeal2 | Mm_Celera | 9:110648662 | ATAGTTCCTGCTTGG[G/T]CATGCAACTGCCATT | 235627 |
rs33297094 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nbeal2 | Mm_Celera | 9:110640747 | CAGGGGAGTCACCTA[A/G]CTCTGCCTGACTTGA | 235627 |
rs33297096 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nbeal2 | Mm_Celera | 9:110640802 | AGAAAGTCACACTGG[A/G]CAATAAGCACGGGAG | 235627 |
rs33297098 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nbeal2 | Mm_Celera | 9:110640879 | CCAGGTGTGAAGCCT[A/G]TAGTCCTCTTCCATC | 235627 |
rs33297100 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nbeal2 | Mm_Celera | 9:110640900 | CTCTTCCATCAGGTG[C/T]TGGGCCAGGGCACAG | 235627 |
rs33297102 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Nbeal2 | Mm_Celera | 9:110642147 | GGGTGGTGCTCGGCT[A/G]GCATGCAGAACGTGC | 235627 |
rs33297524 | snp | C/T | 0.375 | 0.216506 | synonymous-codon | Nbeal2 | GRCm38.p3 | 9:110631083 | TCGCATACGGGAGTA[C/T]GTCTCTGCACTAGAC | 235627 |
rs33298044 | snp | A/C | 0.124444 | 0.216185 | missense | Nbeal2 | Mm_Celera | 9:110642269 | CCTGCACAGAGCCAG[A/C]ACTCACAGCCATCTG | 235627 |
rs33629139 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nbeal2 | Mm_Celera | 9:110653221 | TGCAAGGAGGGAGGC[A/G]TAACCCCGGGATCAC | 235627 |
rs33707247 | snp | C/T | 0.32 | 0.24 | intron-variant | Nbeal2 | GRCm38.p3 | 9:110652351 | CGCCCTTGCCTTACA[C/T]ACCCCGTGACACACA | 235627 |
rs46515230 | snp | A/G | | | synonymous-codon | Nbeal2 | Mm_Celera | 9:110644463 | GCAGGGCTTGATCCA[A/G]GTCGTCCTGGTCCAG | 235627 |
rs211984744 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110634553 | ATCCTGACAGATGCT[A/G]CTGCTCCCTCTACTG | 235627 |
rs212085426 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nbeal2, Mir8107 | GRCm38.p3 | 9:110636254 | CCCACCGTCCAGAAG[A/G]CCTCCCCTGTCTCTC | 235627 |
rs212162598 | snp | C/G | | | upstream-variant-2KB, downstream-variant-500B | Nradd, Nbeal2 | Mm_Celera | 9:110624563 | GAAGCCGACACCAGC[C/G]TGCCTGGCAGAGCAG | 235627 |
rs212231463 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110647018 | GATCTGGGCTACTGG[A/G]AAGGGGAGGAAGTGC | 235627 |
rs212278467 | snp | G/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110647696 | AGGTGTAGTGAGAGA[G/T]CCTGTCTCAGACAAT | 235627 |
rs212342832 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nbeal2, Mir8107 | GRCm38.p3 | 9:110637313 | CTGATGCCCTGGAAT[C/T]AGGACAATGGGGTAG | 235627 |
rs212507518 | snp | A/G | | | upstream-variant-2KB, synonymous-codon | Nradd, Nbeal2 | GRCm38.p3 | 9:110626331 | CCCTGCTGACAGACC[A/G]CTCTGTGGGAAGGCA | 235627 |
rs212721298 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110640639 | GCCATGGTTGAGCCC[C/T]CTGGGCCCTCTGCAC | 235627 |
rs212845506 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110648798 | AGCTATGTGAAGAAG[C/T]TCACGCCCAGTACAG | 235627 |
rs212847994 | snp | C/T | | | missense | Nbeal2 | Mm_Celera | 9:110638536 | ACGGCGCCTGCATGG[C/T]GAGCCTTCTGAGATT | 235627 |
rs212905548 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110649514 | AACTTGCTGCCTTAG[A/G]CAGGGAAGAGCTCCA | 235627 |
rs213041537 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110639459 | CACTCCCTTCGGCTG[C/T]GGAACACCTTCGCTA | 235627 |
rs213057893 | snp | G/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110629487 | CACATCTTAGTCGCA[G/T]GTAAACTACTCAGGG | 235627 |
rs213114987 | snp | C/T | | | missense | Nbeal2 | Mm_Celera | 9:110628401 | CTCCTCACCAGAGCC[C/T]GGCGGTGTTTCTGGA | 235627 |
rs213421825 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110652159 | GCGCTGCTGGCTGGT[C/T]GGCTGTGGACTGACA | 235627 |
rs213783709 | snp | A/G | | | missense | Nbeal2 | Mm_Celera | 9:110630829 | CCTAACTGCTCCTCA[A/G]GCAGCTCCTCCGGAG | 235627 |
rs213978371 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110645158 | GTCCCAGGATGTACA[C/T]ACAGGGTTGGACGGC | 235627 |
rs214031531 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110646208 | ATACCCTGACCTGGA[C/T]GGATGCCAGCAGAGA | 235627 |
rs214065378 | in-del | -/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110627975 | TCCTTCACCACTGTC[-/T]TCCCCACAGTCCTCA | 235627 |
rs214105423 | snp | C/T | | | synonymous-codon | Nbeal2 | Mm_Celera | 9:110634831 | TATCCTCTGGCGGTT[C/T]CGCTCGGGTAACCGC | 235627 |
rs214177842 | in-del | -/CT | | | intron-variant | Nbeal2 | Mm_Celera | 9:110647292 | TGACCCTCTCAGACA[-/CT]CTATCAGAGAGATGG | 235627 |
rs214551101 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110647758 | TAATTTTTATGTGCA[C/T]TGGTGTTTTGCCTGC | 235627 |
rs214609146 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110648615 | GAATATTGGGAGAGA[A/G]AGCTCCCCTCCCAAG | 235627 |
rs214609504 | snp | C/T | | | synonymous-codon, upstream-variant-2KB | Nbeal2, Mir8107 | Mm_Celera | 9:110637395 | CCTTAGGGCAGATGG[C/T]TGCAGGGCTTCATGG | 235627 |
rs214808544 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110626407 | AGGGTTGGGGGGTAA[C/T]GGAGCCCCAGACTTG | 235627 |
rs214852305 | snp | C/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110649635 | ACTGGAGTCAGATAG[C/G]TCTGAACTACATAGC | 235627 |
rs215073468 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110630617 | TTTTTCTGAGCCTTG[C/T]TCAGGGGTGCTTAGC | 235627 |
rs215092630 | in-del | -/A | | | intron-variant | Nbeal2 | Mm_Celera | 9:110647555 | CATAAGCATAGAGAC[-/A]CCGAACTTCCATCCC | 235627 |
rs215147574 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110650637 | GTTCAATTCTTGAGA[A/G]TGACACAGTGATCAG | 235627 |
rs215206378 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110640758 | CCTAGCTCTGCCTGA[C/T]TTGAAGTTGGATGCA | 235627 |
rs215244645 | snp | A/C | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110627439 | TTGACCCCAGGGACA[A/C]AGTGGGTGTCATAGA | 235627 |
rs215285680 | in-del | -/TA | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110650049 | CCAGCCTTCCCCCCC[-/TA]CCCCCAACTCCAGGC | 235627 |
rs215680437 | snp | C/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110643639 | AGGAGTCCCTGTCTA[C/G]TGATGGGATTAGGCA | 235627 |
rs215721665 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110632550 | GGTCACTCACTGTAA[A/G]GTATACCCAGCCCAA | 235627 |
rs215740685 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110644798 | GAGTTCTAGAGGATA[A/G]ATGGATTCTAGGTGG | 235627 |
rs215975568 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110629763 | AAACAGGGTCTAGGA[C/T]GCTTACCTGGGTAAG | 235627 |
rs216022765 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110653574 | ATGCGCCTCTCAGGC[A/G]AAGCAACCAACCAGC | 235627 |
rs216151002 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | Nradd, Nbeal2 | Mm_Celera | 9:110624437 | GGGGCGGGCCAGTGG[A/G]GGGGTGGTGTTGAAG | 235627 |
rs216187209 | snp | A/G | | | upstream-variant-2KB, intron-variant | Nradd, Nbeal2 | Mm_Celera | 9:110625654 | GTAACACATGCTAGT[A/G]AGTGGGTAGTATGCA | 235627 |
rs216584365 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110638268 | TTCCCTCCTGCTCAC[C/T]CTGGCCGTGGATCCC | 235627 |
rs216654841 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110652265 | TCCTCCTGCCTCAAC[C/T]TCTCTCATGCTGGCA | 235627 |
rs216719826 | snp | C/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110628330 | GAAGCGGCAGTCAAC[C/G]CAGGGACTGAATCCC | 235627 |
rs216748148 | snp | G/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110646340 | GCATGGGTGTGTGTG[G/T]GGGGGTGCATGCTTG | 235627 |
rs216872845 | snp | C/T | | | upstream-variant-2KB | Ccdc12, Nbeal2 | Mm_Celera | 9:110654912 | CAACACCCTGTCTGT[C/T]CTTTCCTTGTGACTG | 235627 |
rs216880110 | snp | A/G | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110627553 | GAAGACGCCAGGGTC[A/G]AGCCCGGGCTCAGCC | 235627 |
rs216880181 | snp | A/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110639404 | CCTCCTGAAAAGTAG[A/T]GTGGAAGCAAGCAAA | 235627 |
rs217106814 | snp | C/T | | | synonymous-codon | Nbeal2 | GRCm38.p3 | 9:110630052 | GTGGACCTCACGCAG[C/T]TGGGCCAAGGGGCGC | 235627 |
rs217120980 | in-del | -/GG | | | splice-acceptor-variant | Nbeal2 | Mm_Celera | 9:110644303 | GTTCTCTAGGTTCCT[-/GG]GGGGGGGGGGGTGAA | 235627 |
rs217334109 | snp | A/G | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110630770 | ATCCCTGGCAGCCCC[A/G]GCCCACCACTCACAG | 235627 |
rs217569145 | snp | A/G | | | utr-variant-5-prime | Nbeal2 | Mm_Celera | 9:110654148 | CCTCCTCCTCCTCCC[A/G]GCCGGCCACCGCCTG | 235627 |
rs217587370 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110646922 | CCATCAGCACCACCA[C/T]CCGGCTTTAGTGGGG | 235627 |
rs217628347 | snp | A/G | | | upstream-variant-2KB | Ccdc12, Nbeal2 | Mm_Celera | 9:110655196 | GCTTAGGAAACGGTG[A/G]CATTTGAAGGGAGCT | 235627 |
rs217897457 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110648717 | GGTGGGCTGAGGGCA[A/G]GTCTATTTGGCACTG | 235627 |
rs218131675 | snp | C/T | | | upstream-variant-2KB | Ccdc12, Nbeal2 | Mm_Celera | 9:110654790 | GGTGCCTCATGCCGG[C/T]TTTAATGAATGAAGA | 235627 |
rs218351256 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110648357 | GAGCCTACAAGTTGT[A/G]TCTGTGGGGGGCTTG | 235627 |
rs218633569 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110640996 | GGTGAGGCACGTGAC[A/G]TATTTTAAGAAGCCA | 235627 |
rs218662729 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110651941 | ACACTCTGATACTGT[C/T]CCCTCCCTCTCACTC | 235627 |
rs218680975 | in-del | -/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110641552 | GTTAGAACAGGACCA[-/G]GGGGGAGCTGCTGGG | 235627 |
rs218747817 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110642580 | TGGGGCAGAATGTCA[C/T]GGCTGTACGCTAGAG | 235627 |
rs218863565 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110650788 | CTAGAGGTGGCCCAG[C/T]GGTTAGGGGCATTGT | 235627 |
rs219193943 | snp | A/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110649081 | CCTTTGGAAGACACA[A/T]CCCATTGCTGCACAG | 235627 |
rs219203728 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110649857 | GGACAAAGAGGACCT[A/G]AAGGCCCCATAACAC | 235627 |
rs219342612 | in-del | -/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110645520 | TATGGCATATGTAGT[-/G]GGGGGTCACATTGCC | 235627 |
rs219415407 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110644001 | CCTGTCTGAGGGCTG[A/G]GTCTCACCCAGTGAG | 235627 |
rs219516331 | snp | C/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110652810 | TTCTCTTCACATGGT[C/G]ATCTCCCTTGAAGAT | 235627 |
rs219524921 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110643111 | CTCCAGCTACCCCCA[C/T]CCCACCCCACCCCCA | 235627 |
rs219542919 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110644902 | CCAGAGGACTGTGGT[A/G]TGGACAGGTCACCTC | 235627 |
rs219625820 | snp | A/G | | | synonymous-codon | Nbeal2 | Mm_Celera | 9:110643728 | TTGGAAGAAGGCTCC[A/G]AATTCACAGGGCAAG | 235627 |
rs219711377 | snp | A/G | | | synonymous-codon | Nbeal2 | Mm_Celera | 9:110642225 | CTGAGCAGGGCCACG[A/G]CCCCAGCCCCGCACC | 235627 |
rs219782378 | snp | A/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110650404 | CGTAGGAATCTGACT[A/T]AGCCGGTAAAGCCCC | 235627 |
rs219873936 | in-del | -/TGT | | | intron-variant | Nbeal2 | Mm_Celera | 9:110653038 | GAAGACCAAAGAAGC[-/TGT]GGCCCTTCAGACTTA | 235627 |
rs220005533 | snp | A/C | | | upstream-variant-2KB | Ccdc12, Nbeal2 | Mm_Celera | 9:110655917 | ATAGCAAGGCTTATG[A/C]GCAACAACTCATCAG | 235627 |
rs220137331 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110647320 | TGGCGTGAATACATC[A/G]GGGCTTCTAGAGCAT | 235627 |
rs220146289 | in-del | -/A | | | intron-variant | Nbeal2 | Mm_Celera | 9:110643597 | CTCTCCCCCTAGAGG[-/A]TTCCCGTGTCTCAGG | 235627 |
rs220267806 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110646430 | TCACTCTCCATACGG[C/T]CTCTCAAGTCCCCAG | 235627 |
rs220358975 | snp | G/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110635288 | TCACCCTCCCCAACC[G/T]CCAGCCTACCTGGCC | 235627 |
rs220549952 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110648490 | AAGCCCACCCAAGAG[C/T]CCTTCAGCCCAGGAG | 235627 |
rs220561302 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110648878 | CGCAATCAGTCAGTC[A/G]CCACTCTGGCACAGG | 235627 |
rs220561665 | snp | C/G | | | intron-variant, upstream-variant-2KB | Nbeal2, Mir8107 | Mm_Celera | 9:110637839 | CACTGGTCCAAGCCC[C/G]TCCAACTGACCCATG | 235627 |
rs220635072 | snp | A/G | | | missense | Nbeal2 | Mm_Celera | 9:110634191 | GTCCGTAGATGAGGT[A/G]AAAGAGCTGCCAAAC | 235627 |
rs220655689 | in-del | -/TGGGGG | | | splice-acceptor-variant | Nbeal2 | Mm_Celera | 9:110643796 | AGCTGATGACTTCCC[-/TGGGGG]TGGGGGTGGGGGTGG | 235627 |
rs220784602 | in-del | -/A | | | intron-variant | Nbeal2 | Mm_Celera | 9:110630668 | TTTTAAATAACCCCC[-/A]AAACTTGGGGTTGGA | 235627 |
rs220894698 | in-del | -/TAT | | | intron-variant | Nbeal2 | Mm_Celera | 9:110646691 | GACACTGAGAAGCCG[-/TAT]TACCTGCACGGTTAC | 235627 |
rs220998039 | snp | A/C | | | intron-variant, upstream-variant-2KB | Nbeal2, Mir8107 | Mm_Celera | 9:110637067 | ACGGTTCCCTAACCC[A/C]TAAGTACCTGCGGTG | 235627 |
rs221017271 | snp | C/T | | | synonymous-codon, upstream-variant-2KB | Nbeal2, Mir8107 | GRCm38.p3 | 9:110637641 | CCCTGTGGTGGTTGT[C/T]GTTGTGCGGTGCCCA | 235627 |
rs221090643 | snp | C/T | | | synonymous-codon | Nbeal2 | Mm_Celera | 9:110626776 | CCTGCCACGGGGTAG[C/T]GAAGTCACTCGTAGG | 235627 |
rs221205948 | snp | C/T | | | synonymous-codon | Nbeal2 | GRCm38.p3 | 9:110630242 | GAAATACACGTGCTG[C/T]GTGGTGATCTCTAAG | 235627 |
rs221217896 | in-del | -/CCAAGCTCCAGCCACA | | | intron-variant | Nbeal2 | Mm_Celera | 9:110647385 | AGAAAAGACTCAGCC[-/CCAAGCTCCAGCCACA]CCTTTTGGGCTGAAG | 235627 |
rs221231359 | snp | C/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110642963 | GAGGAACCGGATAGG[C/G]ATGGGGACAGGAGAG | 235627 |
rs221286927 | snp | C/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110627604 | CTCCTTGGCCTCGGC[C/G]CAGTGACAGCAGGAA | 235627 |
rs221376525 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110640000 | TCCCCTGTGAACACC[A/G]GGACCTCTCCTTGCC | 235627 |
rs221393793 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110641610 | GTCAAAGTTCTCCTA[A/G]CAGAGTAGGGCCAGA | 235627 |
rs221451379 | snp | A/G | | | synonymous-codon | Nbeal2 | Mm_Celera | 9:110633931 | GTCAAAGGGTGTACT[A/G]AACGGGGAGAGGGCC | 235627 |
rs221537402 | snp | G/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110644308 | TCTAGGTTCCTGGGG[G/T]GGGGGGTGAAGAACA | 235627 |
rs221562645 | snp | G/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110645216 | ACAACAGCCCACCCT[G/T]GCCCTGAAACCTCTA | 235627 |
rs221814048 | snp | C/T | | | synonymous-codon | Nbeal2 | Mm_Celera | 9:110628916 | CAGGGACGTGAAGGG[C/T]TCCACGCGGATGAGG | 235627 |
rs222129677 | in-del | -/G | | | intron-variant, upstream-variant-2KB | Nbeal2, Mir8107 | Mm_Celera | 9:110636536 | CCCCACCCCCACCCC[-/G]GAGTCCAGGAGTGAA | 235627 |
rs222155865 | snp | G/T | | | synonymous-codon | Nbeal2 | GRCm38.p3 | 9:110631464 | GCGCAATCCCTCCAC[G/T]CGAGCCCTGCGCTGG | 235627 |
rs222326080 | snp | C/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110641523 | AGCAGAGGAGAAGGA[C/G]ATGAGGAGAAGAGGT | 235627 |
rs222352188 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110628538 | GCAGTGTGCCTGAGG[A/G]TTCTTCACCATCCCT | 235627 |
rs222374434 | snp | G/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110630165 | ATTCTCTGTCGCCCC[G/T]TCCAACAGCTCCATC | 235627 |
rs222492675 | snp | C/T | | | synonymous-codon, upstream-variant-2KB | Nbeal2, Mir8107 | Mm_Celera | 9:110637506 | GCTGACGCTGCCCTC[C/T]TGCAGAGGGGTCCCC | 235627 |
rs222492878 | snp | A/G | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110627783 | CATCTTACACAAGAA[A/G]CTAAGTTCCCACCCA | 235627 |
rs222515266 | snp | A/G | | | upstream-variant-2KB, utr-variant-3-prime | Nradd, Nbeal2 | Mm_Celera | 9:110625070 | GTGCAGTAGTCTCCT[A/G]GGCAGAGAATCAGGC | 235627 |
rs222525730 | in-del | -/GCGC | | | intron-variant | Nbeal2 | Mm_Celera | 9:110651111 | TCAGTGTGTGTGTGT[-/GCGC]GTGCACGTGCGTGCA | 235627 |
rs222551945 | snp | A/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110626657 | GGGGAGGACACACAG[A/T]GTTGTCACAGGCCCA | 235627 |
rs222685532 | snp | G/T | | | synonymous-codon, upstream-variant-2KB | Nbeal2, Mir8107 | Mm_Celera | 9:110636605 | GCCCTGAGTGTTGCG[G/T]CCTGAGGTCAGCTCA | 235627 |
rs222697047 | in-del | -/CTTA | | | intron-variant | Nbeal2 | Mm_Celera | 9:110649243 | GGAGGCTGGTGGGGT[-/CTTA]CTACGTAGACCAAGC | 235627 |
rs222886716 | in-del | -/CT | | | intron-variant | Nbeal2 | Mm_Celera | 9:110643013 | CCTGAGGATGTCAGG[-/CT]ACCACTGGAGGGTCC | 235627 |
rs222919360 | snp | C/T | | | synonymous-codon | Nbeal2 | Mm_Celera | 9:110633099 | CTCCACGCCCCGCCA[C/T]GTCACTGAGAATAGC | 235627 |
rs223006092 | in-del | -/CC | | | intron-variant | Nbeal2 | Mm_Celera | 9:110630663 | ACCCTTTTTAAATAA[-/CC]CCCAAAACTTGGGGT | 235627 |
rs223193047 | snp | A/G | | | intron-variant, downstream-variant-500B | Nbeal2, Mir8107 | Mm_Celera | 9:110635531 | GAAACAGGCAGGTAA[A/G]CTGGGGCAGAACGTC | 235627 |
rs223375273 | snp | A/C | | | upstream-variant-2KB, utr-variant-3-prime | Nradd, Nbeal2 | Mm_Celera | 9:110624809 | TACAAAACTAGGCCA[A/C]GTTTATTGCTGAGAA | 235627 |
rs223688649 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110632695 | TCAGGTTATAAGGAC[A/G]CAGAATGTGTGTGGC | 235627 |
rs223852947 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110631200 | TAAGACTGCTGGGGT[C/T]TTAAAGTGCTGGGAA | 235627 |
rs223880634 | snp | C/T | | | upstream-variant-2KB | Ccdc12, Nbeal2 | GRCm38.p3 | 9:110656151 | ACGTGCACCACCTCA[C/T]CCGGCTCAGGGAATG | 235627 |
rs223946154 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110653128 | ATCCCTGCTCTCCCA[A/G]TGACAAGCTGTTCAT | 235627 |
rs224037406 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110652145 | GGGAGGGGCCACCTG[C/T]GCTGCTGGCTGGTTG | 235627 |
rs224153519 | snp | C/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110627740 | CAAGATGTCTGCTCA[C/G]AGATGGGTAAGGACG | 235627 |
rs224210769 | snp | C/T | | | missense | Nbeal2 | Mm_Celera | 9:110628435 | AATCCTCGGGGCTGC[C/T]GGCCCACGGGGGCAG | 235627 |
rs224334280 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110650082 | TATGCTAATTTTTTT[A/G]TCATTAAAGTTCCCT | 235627 |
rs224564272 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110651210 | TGCCAGGTGCTGTCC[C/T]CATCTCCTGGTCCTC | 235627 |
rs224818926 | snp | A/C | | | upstream-variant-2KB | Nbeal2 | Mm_Celera | 9:110654417 | GAATTATCGCTGTTC[A/C]ATGAAAGGACTGTGG | 235627 |
rs224842212 | snp | A/G | | | missense | Nbeal2 | Mm_Celera | 9:110634166 | GCCAGCAGCCGAACG[A/G]CGTCTGGCTGTCCGT | 235627 |
rs224948079 | snp | A/G | | | upstream-variant-2KB, synonymous-codon | Nradd, Nbeal2 | Mm_Celera | 9:110625356 | CCCAGCGCCCACAAC[A/G]ATCAATTTGCCATCT | 235627 |
rs225045775 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110646345 | GGTGTGTGTGGGGGG[A/G]TGCATGCTTGCATGT | 235627 |
rs225078549 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110648592 | AACCAGCCCCAAATA[C/T]ACTCTAAGAATATTG | 235627 |
rs225161304 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110647728 | AGGTAGAGTGAGGAA[A/G]TCACATATAATTACT | 235627 |
rs225187947 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110651446 | GGTGAAGAGGGGGGT[A/G]TCAGAATGAGAAAGA | 235627 |
rs225190457 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110640653 | CCCTGGGCCCTCTGC[A/G]CCCAGCTCTACCAAG | 235627 |
rs225288904 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110650507 | AGGCAGGGGCAGGAC[A/G]CCACCACAGGCAGAG | 235627 |
rs225394270 | snp | G/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110646548 | CTCAGGCTCCCTGCT[G/T]GTGAAGCAAATACCA | 235627 |
rs225401114 | snp | C/T | | | upstream-variant-2KB | Ccdc12, Nbeal2 | Mm_Celera | 9:110655568 | AGTAATTCAGTGGCA[C/T]TTATTCGGCCCTGGT | 235627 |
rs225465529 | in-del | -/TCCTTCCACTGGGCAGA | | | upstream-variant-2KB | Ccdc12, Nbeal2 | Mm_Celera | 9:110654637 | TGCAGAGGAGCGGCG[-/TCCTTCCACTGGGCAGA]TCCTTACCAAGTTTA | 235627 |
rs225485875 | snp | C/G | | | missense | Nbeal2 | Mm_Celera | 9:110642203 | CCAGTGGCACCTGCT[C/G]GGGGTCCTGAGCAGG | 235627 |
rs225702914 | snp | A/G | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110648738 | TTTGGCACTGGTTGG[A/G]AGAAAGCTTTCCACC | 235627 |
rs226138051 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110647374 | GTGGAAAGCCTCAGA[A/G]AAGACTCAGCCCCTT | 235627 |
rs226291057 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110644598 | GCAGTCCTACCTGCC[C/T]GGCCCTGGCCTCTGT | 235627 |
rs226315037 | snp | C/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110653392 | ATCCTCCCTGGCCCA[C/T]TGCAGAATGGAGGTA | 235627 |
rs226372924 | snp | C/T | | | upstream-variant-2KB | Ccdc12, Nbeal2 | Mm_Celera | 9:110655047 | TCGATCAGTATGAAG[C/T]GCCCTATGCATCTTA | 235627 |
rs226374980 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110643630 | AGACCACCAAGGAGT[C/T]CCTGTCTAGTGATGG | 235627 |
rs226390632 | snp | C/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110649754 | GGGATGGAGCCGGAA[C/G]ATTCAACCTGCCCAT | 235627 |
rs226391327 | in-del | -/CTCC | | | intron-variant | Nbeal2 | Mm_Celera | 9:110647106 | TGGCCTGTGCGCATT[-/CTCC]CTCCCGTCCTTTGTG | 235627 |
rs226392707 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110647597 | ATCAGAAAAAGCAGC[A/G]CTTGTTCTAATCTCA | 235627 |
rs226393745 | snp | A/G | | | synonymous-codon, downstream-variant-500B | Nbeal2, Mir8107 | GRCm38.p3 | 9:110635955 | CCCACCGCCATCAGC[A/G]GCCGCCTGCTCCATC | 235627 |
rs226478729 | snp | A/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110648946 | TTTGAGGCCCTGTGT[A/T]TGTGCTGGCCCTCAT | 235627 |
rs226487871 | snp | C/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110639890 | GGGGAAGTCAGGAGA[C/T]GTAGCTGCCAGGGTG | 235627 |
rs226533360 | snp | A/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110645692 | CCACCTGGTTTCCGC[A/T]GGTCTTTTGCTTGGT | 235627 |
rs226586359 | snp | C/T | | | utr-variant-5-prime | Nbeal2 | Mm_Celera | 9:110654124 | CTTAGCCACCAAAGT[C/T]TACACGCCCCTCCTC | 235627 |
rs226606973 | snp | C/T | | | synonymous-codon, upstream-variant-2KB | Nbeal2, Mir8107 | Mm_Celera | 9:110637132 | TAGTTCACCCTCAGG[C/T]TTGAAGGGTGCTGGC | 235627 |
rs226854130 | snp | C/T | | | missense | Nbeal2 | Mm_Celera | 9:110638863 | ACTGGCTGCTCGTTG[C/T]GGATTGGTGGAGGTG | 235627 |
rs226977345 | in-del | -/A | | | intron-variant | Nbeal2 | Mm_Celera | 9:110640555 | GAGATTGAGAGTCAG[-/A]AGCAGACTGCTCGCT | 235627 |
rs227127933 | snp | A/C | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110643033 | ACTGGAGGGTCCTAC[A/C]AATGGGTGGGAACAA | 235627 |
rs227208263 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110641946 | TCCCCTCCTGGCCAG[C/T]CAGCCCTGCCTTTCC | 235627 |
rs227345387 | in-del | -/CC | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110650043 | AAGGATACCAGCCTT[-/CC]CCCCCCCCCCAACTC | 235627 |
rs227372482 | snp | A/G | | | synonymous-codon | Nbeal2 | GRCm38.p3 | 9:110639305 | TCACCATGTTGAGCA[A/G]TTCCTGCAACAGCCT | 235627 |
rs227377114 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110651312 | CCTGCTCCCTACTTC[A/G]GACAACTTGATGCTG | 235627 |
rs227414005 | snp | C/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110630732 | AAGACGCAGACTCAG[C/T]CCCAGCTGCACAGAA | 235627 |
rs227415809 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110643246 | TGCTGGCCACTGGCT[C/T]TCCCATGAGAGGAGA | 235627 |
rs227514818 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110648648 | TTAGTGAGGCACAGA[C/T]AGTTCCTGCTTGGTC | 235627 |
rs227588446 | in-del | -/CTT | | | intron-variant, upstream-variant-2KB | Nbeal2, Mir8107 | Mm_Celera | 9:110636189 | AGGGCTACGGCCCAA[-/CTT]CTTCTGCTGCCATCA | 235627 |
rs227599779 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110643401 | CACAGGGGCTGGAGG[A/G]GGGGTAGAGCCTGGG | 235627 |
rs227734094 | snp | A/C | | | synonymous-codon | Nbeal2 | Mm_Celera | 9:110632077 | CTCAGTCTCGGAAGA[A/C]GAGGTGGTCAGCGCC | 235627 |
rs227735093 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110640164 | CTGGCCACAGTTAAC[A/G]GTCCTTCAGGGCTGT | 235627 |
rs227745292 | snp | A/G | | | synonymous-codon | Nbeal2 | GRCm38.p3 | 9:110629166 | CACACCGATGGGTTT[A/G]GACAGGTCCCGGAAG | 235627 |
rs227935157 | snp | A/C | | | intron-variant | Nbeal2 | Mm_Celera | 9:110633360 | GGTTCTGTTGGACTT[A/C]AGAGAGGAGATATTC | 235627 |
rs228047539 | snp | A/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110646004 | GCTGGGGCCTTTAAA[A/T]CAGCGCCTTATGGTG | 235627 |
rs228344309 | snp | A/G | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110634311 | CCCAGAAAGGCAAAA[A/G]GAGCTCCAGGGAGCA | 235627 |
rs228377098 | in-del | -/G | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110644304 | GTTCTCTAGGTTCCT[-/G]GGGGGGGGGGTGAAG | 235627 |
rs228423103 | snp | C/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110634558 | GACAGATGCTACTGC[C/T]CCCTCTACTGCACCT | 235627 |
rs228709561 | snp | C/T | | | upstream-variant-2KB, missense | Nradd, Nbeal2 | Mm_Celera | 9:110626037 | GTGCTAAGTGCGATA[C/T]AGGTCCAGGCAGTGT | 235627 |
rs228716293 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nbeal2, Mir8107 | GRCm38.p3 | 9:110638057 | CTCCATGCTCTCACC[C/T]CACCCTGGGCCACAT | 235627 |
rs228857489 | in-del | -/GGTA | | | intron-variant | Nbeal2 | Mm_Celera | 9:110641071 | CTCAGGGACTGCCTT[-/GGTA]GGTAAGTGATGACAA | 235627 |
rs228858830 | snp | A/C | | | intron-variant, upstream-variant-2KB | Nbeal2, Mir8107 | Mm_Celera | 9:110637200 | CCTTAGGTCTTCTGG[A/C]CAAACCCTCTCCATA | 235627 |
rs228880873 | in-del | -/AG | | | intron-variant | Nbeal2 | Mm_Celera | 9:110649936 | TATCACTATGGAAAC[-/AG]AGTTCCCTGCCATGG | 235627 |
rs228984993 | snp | A/G | | | intron-variant, downstream-variant-500B | Nbeal2, Mir8107 | Mm_Celera | 9:110635797 | CTCAGATTATAGAGG[A/G]AGGCTGTGGCTTCTC | 235627 |
rs229025113 | snp | A/G | | | synonymous-codon | Nbeal2 | Mm_Celera | 9:110627083 | CCTGCCTTACTTGGG[A/G]CTCCCCATGGTGGGA | 235627 |
rs229039567 | in-del | -/CAGTAGCC | | | upstream-variant-2KB | Ccdc12, Nbeal2 | Mm_Celera | 9:110654662 | AGTTTAGGATACATA[-/CAGTAGCC]CACTCCCTCTAGGAA | 235627 |
rs229091136 | snp | A/G | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110628157 | ACTGTCTGTGCCCTG[A/G]CCCCATCTCACGTGC | 235627 |
rs229170875 | in-del | -/AACACAC | | | intron-variant | Nbeal2 | Mm_Celera | 9:110649881 | TAACACATAACACAT[-/AACACAC]AACATATAACATAAG | 235627 |
rs229255752 | snp | A/G | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110629450 | GGGCAGGGGAGCGAG[A/G]CAGTGTCAGAGACCA | 235627 |
rs229318467 | snp | G/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110638943 | CAATCCCGGTCACTG[G/T]TGGCCCCTTGCCAGC | 235627 |
rs229557679 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110630415 | CAAGCTCCGAGACCA[A/G]TGAGCCATGAGGTCA | 235627 |
rs229671550 | snp | C/T | | | synonymous-codon, upstream-variant-2KB | Nbeal2, Mir8107 | Mm_Celera | 9:110638104 | CACCCAGGCAGAATC[C/T]GCGAAGGACACTTCG | 235627 |
rs229689681 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110630126 | TAAGGAGTCACTGGT[C/T]CCAGCCCAGCCTGCA | 235627 |
rs229700254 | snp | C/T | | | synonymous-codon | Nbeal2 | Mm_Celera | 9:110627308 | GATAAAGGAGTGTGA[C/T]TGTCGGTGAGGAACC | 235627 |
rs229955734 | snp | C/G | | | synonymous-codon | Nbeal2 | GRCm38.p3 | 9:110630792 | CACTCACAGGGACTC[C/G]AGTGCAGCCAGGTCC | 235627 |
rs230104610 | snp | C/T | | | upstream-variant-2KB | Nbeal2 | Mm_Celera | 9:110654335 | AGCCACTGGCAGGAT[C/T]ATTTCCATCCTCCCC | 235627 |
rs230220868 | snp | A/G | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110630462 | TGATGGAGAGGAGCT[A/G]CCCAGGGCCTCCTGC | 235627 |
rs230301781 | snp | C/T | | | upstream-variant-2KB | Ccdc12, Nbeal2 | Mm_Celera | 9:110655481 | ACCTGCCTCTGCCTC[C/T]CAAGTGCCGGGATTA | 235627 |
rs230399398 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110629710 | TTGAAGTTGTCCAGA[A/G]CCCCCTATCTACAAA | 235627 |
rs230526877 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110646374 | GTGCATGCATGCATG[C/T]ATGTGTGTGTAGAGC | 235627 |
rs230788223 | in-del | -/TG | | | intron-variant | Nbeal2 | Mm_Celera | 9:110648382 | GCTTGAGATCTGTAT[-/TG]CTTTCTCAGAGCCTC | 235627 |
rs230805655 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110647055 | ACATACCAGAAGGGT[A/G]TGAAGAAGTCGTGTC | 235627 |
rs230852964 | snp | G/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110633442 | AGTGGGGCTGGAGAA[G/T]TGGTTCAGCAGCTAA | 235627 |
rs231159432 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110634273 | CAAGGTCTTAACAGC[A/G]GGGACCTACAAAGGT | 235627 |
rs231173635 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110648802 | ATGTGAAGAAGCTCA[C/T]GCCCAGTACAGAAAG | 235627 |
rs231312872 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110626924 | AACCAAGGGGAAGAC[A/G]GTAGGTGAGGCTGGG | 235627 |
rs231360955 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110649518 | TGCTGCCTTAGGCAG[A/G]GAAGAGCTCCAAGCA | 235627 |
rs231447338 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110627555 | AGACGCCAGGGTCGA[A/G]CCCGGGCTCAGCCTT | 235627 |
rs231813500 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110649173 | CCCTGTTTAAACACT[A/G]GGTAGCTTGTTAACC | 235627 |
rs231877075 | snp | C/T | | | upstream-variant-2KB, intron-variant | Nradd, Nbeal2 | GRCm38.p3 | 9:110625490 | GAAGTAGGTGTACAC[C/T]GAGTCACAACTGCAA | 235627 |
rs232183962 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110652189 | AAAAAAGGGTCTCTT[C/T]TTTCTTTTTGAGACA | 235627 |
rs232186319 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110641578 | CTGGGGTTCTGCACC[A/G]GTGGGAAACAGTCCT | 235627 |
rs232222050 | snp | G/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110645163 | AGGATGTACACACAG[G/T]GTTGGACGGCAGGCA | 235627 |
rs232243724 | snp | C/T | | | upstream-variant-2KB | Nbeal2 | Mm_Celera | 9:110654373 | GGCCCGTAAAGGCTT[C/T]AACCCGAGTACAGAA | 235627 |
rs232276727 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110651145 | CTCCAGCCTGCAGAG[A/G]GGCTGCTCATTTACA | 235627 |
rs232336217 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110651869 | AACTCTCCTGGTGAC[C/T]TTGCCTTGGTTTCCC | 235627 |
rs232457456 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110646228 | GCCAGCAGAGATGGG[A/G]CAGGCTCCCCCAAAA | 235627 |
rs232475405 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110642818 | GGGACCAGGCTACCA[C/T]GGGGGAGTAGTAGGG | 235627 |
rs232493737 | snp | C/T | | | synonymous-codon | Nbeal2 | Mm_Celera | 9:110634858 | CCGCTCATTCTGCTG[C/T]AGTCTTCGCAAGATC | 235627 |
rs232581355 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110628319 | CCTGAGGGGAGGAAG[C/T]GGCAGTCAACGCAGG | 235627 |
rs232595983 | snp | G/T | | | synonymous-codon | Nbeal2 | GRCm38.p3 | 9:110639320 | ATTCCTGCAACAGCC[G/T]GTGGGTAGGGGGTCC | 235627 |
rs232660257 | snp | A/G | | | upstream-variant-2KB | Ccdc12, Nbeal2 | Mm_Celera | 9:110655170 | ACCAGGTTAACCCAG[A/G]ATAACACCGAGCTTA | 235627 |
rs232785244 | in-del | -/GAGA | | | intron-variant | Nbeal2 | Mm_Celera | 9:110644774 | TCCCACTGAAGAGGG[-/GAGA]GAAAGGTGGAGTTCT | 235627 |
rs232903086 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110644845 | AAAGGCAGAGGACGG[C/T]AGGTCAAGCAGGACG | 235627 |
rs233067296 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110653079 | ATCAGGCAGCCTCTT[C/T]AGAGGGCCAGGGTAG | 235627 |
rs233308598 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110639619 | ACACCCAACTCCCAG[A/G]ATACACTGATGACCA | 235627 |
rs233469902 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110648560 | ATGGATGCTGGTCAT[C/T]GCCCTAACCCGTCCC | 235627 |
rs233496071 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110653107 | TAGAGCATGAACTCT[C/T]CCCATATCCCTGCTC | 235627 |
rs233538303 | snp | A/G | | | synonymous-codon | Nbeal2 | Mm_Celera | 9:110628460 | GGGCAGCACCACATC[A/G]CCCACCTTCTCGTTG | 235627 |
rs233543330 | snp | A/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110640889 | AGCCTGTAGTCCTCT[A/T]CCATCAGGTGCTGGG | 235627 |
rs233652600 | in-del | -/GGGAGGACAGCA | | | intron-variant | Nbeal2 | Mm_Celera | 9:110644393 | GCCTCTGGCCACCCT[-/GGGAGGACAGCA]GGGAGAAACCACCTG | 235627 |
rs233799524 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110647760 | ATTTTTATGTGCACT[A/G]GTGTTTTGCCTGCAT | 235627 |
rs233821224 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nbeal2, Mir8107 | Mm_Celera | 9:110636496 | CTACCTCAAGCACAA[C/T]CCCAAGCACCATACC | 235627 |
rs233903259 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110647323 | CGTGAATACATCGGG[A/G]CTTCTAGAGCATTTC | 235627 |
rs234029058 | snp | A/C | | | intron-variant | Nbeal2 | Mm_Celera | 9:110650249 | ACCCCAGCACTTGGG[A/C]GTTGGATCTCTTAAT | 235627 |
rs234041485 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110640307 | ACTGCCTCTGCACCC[C/T]TCCTGTTCTCTGCTG | 235627 |
rs234137648 | snp | C/T | | | missense, upstream-variant-2KB | Nbeal2, Mir8107 | Mm_Celera | 9:110637496 | CGAGGGTAGAGCTGA[C/T]GCTGCCCTCCTGCAG | 235627 |
rs234226885 | in-del | -/GGAGGAACA | | | intron-variant | Nbeal2 | Mm_Celera | 9:110642938 | GTCTGGGTCACATGG[-/GGAGGAACA]GGAGGAACCGGATAG | 235627 |
rs234375320 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110650863 | GTGACTCAAAACTGA[C/T]TGTAATTCCACTTCC | 235627 |
rs234427187 | in-del | -/TGTATGTATGTA | | | intron-variant | Nbeal2 | Mm_Celera | 9:110647770 | CACTGGTGTTTTGCC[-/TGTATGTATGTA]TGCATGTATGTATGT | 235627 |
rs234467731 | snp | A/C | | | intron-variant | Nbeal2 | Mm_Celera | 9:110641294 | CTGCCAAGTATGTTA[A/C]GCCTCAACGTATCTA | 235627 |
rs234470291 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110647651 | AGGTCGGTGGAGCTC[A/G]AAGGCCACCCAGCCA | 235627 |
rs234565879 | in-del | -/TGTG | | | intron-variant | Nbeal2 | Mm_Celera | 9:110634580 | ACTGCACCTGTCCTT[-/TGTG]TGTGTGTGTGTGTGT | 235627 |
rs234769071 | snp | A/C | | | upstream-variant-2KB, downstream-variant-500B | Nradd, Nbeal2 | Mm_Celera | 9:110624533 | CGGAGCACGCAGAAG[A/C]ACTCGGAGTTCACAG | 235627 |
rs234881153 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110649380 | CCAAGGGTAGGATGA[C/T]AGGGAGCTGCAGGCC | 235627 |
rs235003124 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110643891 | CACCGCTGCCTGGTC[A/G]GGTCACTGGTCATTC | 235627 |
rs235053194 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110632721 | GTGGCTTCCACCCCT[C/T]CGAATAATCGTACCT | 235627 |
rs235139429 | in-del | -/GCCCCG | | | intron-variant | Nbeal2 | Mm_Celera | 9:110630765 | CATCCATCCCTGGCA[-/GCCCCG]GCCCACCACTCACAG | 235627 |
rs235364188 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110633530 | CCTGGGCCCTATGTG[A/G]CTGCTGCTCTCCTCT | 235627 |
rs235415252 | in-del | -/CATACCC | | | intron-variant | Nbeal2 | Mm_Celera | 9:110629736 | ACAAAGTCTTCACCT[-/CATACCC]CACACAAACAGGGTC | 235627 |
rs235536542 | in-del | -/GTGGGG | | | intron-variant | Nbeal2 | Mm_Celera | 9:110646730 | GGCAATGCAAAGGGA[-/GTGGGG]GTGGGGGGAGGGTTG | 235627 |
rs235543802 | snp | C/T | | | synonymous-codon, upstream-variant-2KB | Nbeal2, Mir8107 | Mm_Celera | 9:110637374 | CATACCCAGGCTACA[C/T]AGGACCCTTAGGGCA | 235627 |
rs235655861 | snp | A/G | | | synonymous-codon | Nbeal2 | Mm_Celera | 9:110627810 | CCCACTTCTCACCTC[A/G]GCGAAAAAGGCCTTG | 235627 |
rs235692769 | snp | C/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110628855 | TGCCTTCCTCCCCAC[C/G]CTTCCGTCACCCCTG | 235627 |
rs235766097 | snp | G/T | | | upstream-variant-2KB, intron-variant | Nradd, Nbeal2 | GRCm38.p3 | 9:110626383 | AAATGAAGATTTTAT[G/T]CGAGCCAGAGGGTTG | 235627 |
rs235830500 | in-del | -/CAAA | | | intron-variant | Nbeal2 | Mm_Celera | 9:110645057 | TACCTGCTCTCTACC[-/CAAA]CAAAGCCTTGGCCTG | 235627 |
rs235907562 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110642588 | AATGTCATGGCTGTA[C/T]GCTAGAGGGATTTCA | 235627 |
rs235932226 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110652392 | CTAGCAGCACTATCT[C/T]TCCTTGGGAACCCAG | 235627 |
rs236020458 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110651334 | TTGATGCTGCTTCTC[C/T]TCCTCCTCTTTCAGA | 235627 |
rs236131721 | snp | A/G | | | synonymous-codon | Nbeal2 | Mm_Celera | 9:110628406 | CACCAGAGCCTGGCG[A/G]TGTTTCTGGATGAAA | 235627 |
rs236518849 | in-del | -/TC | | | upstream-variant-2KB | Ccdc12, Nbeal2 | Mm_Celera | 9:110655334 | AAAGAAGCAAACGCA[-/TC]TGTGACCATCTGCCG | 235627 |
rs236547880 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110627579 | CAGCCTTGGTCCCTT[C/T]ATCCCATTACTCCTT | 235627 |
rs236587718 | snp | C/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110628348 | GGGACTGAATCCCAC[C/G]GCAACTCTCAGCCCT | 235627 |
rs236641539 | snp | C/T | | | synonymous-codon | Nbeal2 | Mm_Celera | 9:110633694 | CACCTGGGGGTTGCT[C/T]GTGTTCGAGGTATCA | 235627 |
rs236767340 | snp | C/T | | | missense | Nbeal2 | Mm_Celera | 9:110630905 | TCTCCTCAGTGGGTG[C/T]CATGGGAGCTTCACC | 235627 |
rs237167214 | snp | A/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110648435 | CCTTTCCAGCTCTGA[A/T]GGGGACTCGAAGGAC | 235627 |
rs237256219 | snp | A/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110647589 | ACCACATAATCAGAA[A/T]AAGCAGCGCTTGTTC | 235627 |
rs237286579 | snp | G/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110651054 | GAGAATTCAGCTCAG[G/T]TTCCCTGTCCTGCCA | 235627 |
rs237366397 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | Nradd, Nbeal2 | GRCm38.p3 | 9:110624572 | ACCAGCGTGCCTGGC[A/G]GAGCAGGCCACTGGC | 235627 |
rs237408544 | snp | A/C | | | intron-variant, upstream-variant-2KB | Nbeal2, Mir8107 | GRCm38.p3 | 9:110636289 | CAACCGCGCACCATG[A/C]CTCACCTTGCGCAGG | 235627 |
rs237710999 | snp | C/G | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110646913 | CCACCACCACCATCA[C/G]CACCACCATCCGGCT | 235627 |
rs237918010 | snp | A/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110627477 | GTCTGAGAGGTAGAC[A/T]TGACAGCAGTGGGCA | 235627 |
rs238013290 | snp | C/T | | | upstream-variant-2KB | Ccdc12, Nbeal2 | Mm_Celera | 9:110655825 | CTCCCGAAAGAGATG[C/T]GAGATCATTCTTGAG | 235627 |
rs238040644 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110627610 | GGCCTCGGCGCAGTG[A/G]CAGCAGGAAAGGGGA | 235627 |
rs238238391 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110651684 | TGGTCATCTTCTCAT[C/T]CAGTCATTCAGCTAA | 235627 |
rs238466128 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110649743 | CTGTAGGCCATGGGA[C/T]GGAGCCGGAACATTC | 235627 |
rs238496368 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110643153 | CTGGGGTCATGTACT[A/G]CTGACTTGCTAAATG | 235627 |
rs238552695 | in-del | -/CGAGA | | | intron-variant | Nbeal2 | Mm_Celera | 9:110645908 | GCTTACGAGCCGGGC[-/CGAGA]CTGCTCTTGGGGGCA | 235627 |
rs238570004 | snp | A/C | | | missense | Nbeal2 | Mm_Celera | 9:110644082 | GGGCATGCAGGGCCA[A/C]GTTCTCTAGCTGGGT | 235627 |
rs238739416 | snp | A/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110632493 | TTTGGGGGAGAAAAC[A/T]AGGTAAAGTTTGTGC | 235627 |
rs239011973 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110649087 | GAAGACACAACCCAT[C/T]GCTGCACAGGTAGGG | 235627 |
rs239018000 | snp | C/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110652279 | CCTCTCTCATGCTGG[C/G]ATTACAGGCATGTGC | 235627 |
rs239207827 | snp | A/G | | | upstream-variant-2KB | Ccdc12, Nbeal2 | Mm_Celera | 9:110655557 | TGGGAGGAGAGAGTA[A/G]TTCAGTGGCACTTAT | 235627 |
rs239231395 | snp | C/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110650043 | AAGGATACCAGCCTT[C/T]CCCCCCCCCCCAACT | 235627 |
rs239295508 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110640106 | TAGAGGTCTCAGCTC[A/G]GGGCATTGACAGGTA | 235627 |
rs239405910 | snp | A/G | | | upstream-variant-2KB | Ccdc12, Nbeal2 | Mm_Celera | 9:110655660 | AGCCCTGGCTATCCT[A/G]GAACTCACTTTGTAG | 235627 |
rs239484327 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110647614 | TTGTTCTAATCTCAG[C/T]CAAGGGGAGGCAGAG | 235627 |
rs239596738 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110646924 | ATCAGCACCACCATC[C/T]GGCTTTAGTGGGGTT | 235627 |
rs239744072 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110627756 | AGATGGGTAAGGACG[C/T]GTGGCTAAACCCATC | 235627 |
rs239752232 | snp | A/T | | | intron-variant, upstream-variant-2KB | Nbeal2, Mir8107 | Mm_Celera | 9:110638021 | GGAAGGAAGCTACAG[A/T]GGCTCAAGCCATGTT | 235627 |
rs239843869 | snp | A/G | | | upstream-variant-2KB | Ccdc12, Nbeal2 | GRCm38.p3 | 9:110655082 | GAGCTTACCTTTCCT[A/G]AGCACAGATACCCTC | 235627 |
rs240216875 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110638279 | TCACTCTGGCCGTGG[A/G]TCCCTAGCCCTTGGC | 235627 |
rs240220070 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110626450 | AGGGGAAGGGAGTAA[C/T]GGGGAAGTTCTGATG | 235627 |
rs240239344 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110645751 | ATGCCAATTCCAGGA[C/T]ATGGAGGTGGGACCT | 235627 |
rs240306461 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110648737 | ATTTGGCACTGGTTG[A/G]GAGAAAGCTTTCCAC | 235627 |
rs240454752 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110646472 | TTCTGTCCCAAACAC[C/T]AGGGTCACGAACATG | 235627 |
rs240474680 | snp | A/G | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110634289 | GGGACCTACAAAGGT[A/G]CCCCACCCCAGAAAG | 235627 |
rs240510388 | snp | A/G | | | intron-variant, downstream-variant-500B | Nbeal2, Mir8107 | Mm_Celera | 9:110635593 | GGACCTCCAACATCC[A/G]CCAGGGCCCGCCAGC | 235627 |
rs240613360 | snp | G/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110650645 | CTTGAGAATGACACA[G/T]TGATCAGAAAGCAGA | 235627 |
rs240651971 | snp | A/C | | | intron-variant | Nbeal2 | Mm_Celera | 9:110648896 | ACTCTGGCACAGGCT[A/C]CGCCTTCAGAGCAAA | 235627 |
rs240944115 | in-del | -/CAC | | | intron-variant | Nbeal2 | Mm_Celera | 9:110646889 | ACATGCTACCACCAT[-/CAC]CATCACCACCACCAC | 235627 |
rs240971756 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110633261 | AGAGAGGCAGCATTC[A/G]GCAAACAGCCAGACT | 235627 |
rs241005418 | snp | A/G | | | synonymous-codon | Nbeal2 | Mm_Celera | 9:110634012 | GTCAGAAGAGTCAGC[A/G]GGCAACTCAGTGGGC | 235627 |
rs241023656 | in-del | -/C | | | intron-variant | Nbeal2 | Mm_Celera | 9:110643600 | CTCCCCCTAGAGGTT[-/C]CCGTGTCTCAGGCCA | 235627 |
rs241263634 | snp | A/C | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110641998 | TTCCCAGGGCCTGGG[A/C]GCCCACACCTACCGA | 235627 |
rs241321558 | snp | A/C | | | intron-variant | Nbeal2 | Mm_Celera | 9:110630422 | CGAGACCAGTGAGCC[A/C]TGAGGTCACATGCTC | 235627 |
rs241377397 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110640211 | TCATAAAGACAAAGC[C/T]AGGGCAGATTTGGGC | 235627 |
rs241478449 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110643667 | GCAACTAGGTTTTGG[A/G]GGCAGGACCAGGTGG | 235627 |
rs241563644 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110641630 | GTAGGGCCAGAACCC[A/G]AAGGGACAAACCTTG | 235627 |
rs241574064 | snp | A/C | | | intron-variant | Nbeal2 | Mm_Celera | 9:110629302 | TGCCTGCCAGCCCAC[A/C]CTGCCCTGCCCTCAA | 235627 |
rs241587877 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110653840 | CGGACGCAGGTGCAG[C/T]AGACACTGCGTGCGC | 235627 |
rs241611256 | snp | C/T | | | missense | Nbeal2 | Mm_Celera | 9:110630250 | CGTGCTGTGTGGTGA[C/T]CTCTAAGAGTCCCGG | 235627 |
rs241729679 | snp | A/G | | | synonymous-codon, upstream-variant-2KB | Nbeal2, Mir8107 | Mm_Celera | 9:110636700 | GCTCCAGCAAGGGCA[A/G]CAGAACACCCATGCC | 235627 |
rs242130279 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110644561 | CTGGAAGAGGGGAGC[A/G]AGAGATGCTGAGTGC | 235627 |
rs242211371 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110643488 | AGTGAAGGAAGATGG[A/G]AAATTAAGGGGACAG | 235627 |
rs242230307 | in-del | -/AG | | | intron-variant | Nbeal2 | Mm_Celera | 9:110639572 | GGTGGTCAGCTCACA[-/AG]TGTCCTTTCTCTACA | 235627 |
rs242326772 | snp | G/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110646342 | ATGGGTGTGTGTGGG[G/T]GGGTGCATGCTTGCA | 235627 |
rs242683499 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110626715 | TCTCATTCTCCCTGG[C/T]ACCAGGGCTGCTCAT | 235627 |
rs242741686 | snp | C/T | | | upstream-variant-2KB, utr-variant-3-prime | Nradd, Nbeal2 | Mm_Celera | 9:110625091 | AGAATCAGGCTCGGG[C/T]CGGGTCTGATGTCTG | 235627 |
rs242882667 | in-del | -/GG | | | intron-variant | Nbeal2 | Mm_Celera | 9:110649701 | GCAATGTCAGGCCAT[-/GG]GTGGCTTCTAGCTAC | 235627 |
rs242969178 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110647864 | CCAGTTGATGGGGAA[A/G]AAAACTGCTAGGAAG | 235627 |
rs243046092 | snp | A/G | | | synonymous-codon, upstream-variant-2KB | Nbeal2, Mir8107 | GRCm38.p3 | 9:110637587 | GGTGAGGGAAGGGTG[A/G]GTGTGAGCCAAGGCT | 235627 |
rs243065816 | snp | A/G | | | synonymous-codon | Nbeal2 | Mm_Celera | 9:110626833 | GAGCAGCTTTCCGTC[A/G]GGAGCTACTGCTAGT | 235627 |
rs243152189 | snp | A/G | | | upstream-variant-2KB | Ccdc12, Nbeal2 | Mm_Celera | 9:110655485 | GCCTCTGCCTCTCAA[A/G]TGCCGGGATTAAAGT | 235627 |
rs243307724 | snp | A/G | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110646039 | GCTCACCCCAGCATA[A/G]CTTTTGTTACTTCCT | 235627 |
rs243366208 | snp | G/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110646736 | GCAAAGGGAGTGGGG[G/T]TGGGGGGAGGGTTGC | 235627 |
rs243391802 | in-del | -/GT | | | intron-variant, upstream-variant-2KB | Nbeal2, Mir8107 | Mm_Celera | 9:110636245 | CACTTAGGCCCCACC[-/GT]CCAGAAGGCCTCCCC | 235627 |
rs243541938 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110629028 | TCATATCTGAAGCCA[C/T]AGGCAGCACATGTCA | 235627 |
rs243605631 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110638252 | AAGCTGGTTATGCCC[A/G]TTCCCTCCTGCTCAC | 235627 |
rs243642806 | snp | C/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110628374 | GCCCTGGCTGCCTGT[C/G]TGTGCGATCACCTCC | 235627 |
rs243683744 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110639957 | GGGCCAGGTACACCA[C/T]GGTCCAGGGCATCTG | 235627 |
rs243803932 | in-del | -/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110649137 | ATTGGTGGCTGAGGG[-/T]TATGAGTTTTGGAAC | 235627 |
rs243963222 | in-del | -/GGATGG | | | cds-indel | Nbeal2 | Mm_Celera | 9:110644115 | ATGGCTCTCCTGTGA[-/GGATGG]GGATCCTTTCAGCTG | 235627 |
rs244172541 | snp | C/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110643060 | ACAAATCTAGATGGT[C/T]CTAGGAGTGCCTAGG | 235627 |
rs244278457 | snp | C/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110649568 | CTCAATATGGACAAT[C/G]CCTTTCAGTCAGAGG | 235627 |
rs244346330 | snp | G/T | | | missense | Nbeal2 | Mm_Celera | 9:110632042 | CAGCGCTCAGAGGCT[G/T]CCACGGCTGTAGACG | 235627 |
rs244378498 | snp | C/G | | | missense | Nbeal2 | Mm_Celera | 9:110644529 | GCAGAGGCACTTCCG[C/G]ACCTGCCTCCTCTGG | 235627 |
rs244449053 | snp | A/C | | | intron-variant | Nbeal2 | Mm_Celera | 9:110631282 | TGCATTACTTTCAAG[A/C]CTTGAGCAGAGAGTC | 235627 |
rs244515180 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110650523 | CCACCACAGGCAGAG[C/T]CCTTAAGCTCATTGG | 235627 |
rs244562720 | in-del | -/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110640854 | CAGAGCAGAGGCTCA[-/G]GGGTGGGGACCAGGT | 235627 |
rs244608028 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110653133 | TGCTCTCCCAGTGAC[A/G]AGCTGTTCATGGACA | 235627 |
rs244857255 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110645667 | TTGTTCCTTCCCAGG[A/G]CCTGGCCACCCACCT | 235627 |
rs245046481 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110648612 | TAAGAATATTGGGAG[A/G]GAAAGCTCCCCTCCC | 235627 |
rs245124113 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110647742 | AATCACATATAATTA[C/T]TAATTTTTATGTGCA | 235627 |
rs245174161 | snp | C/G | | | upstream-variant-2KB | Nbeal2 | GRCm38.p3 | 9:110654362 | CCCCAGTGAGGGGCC[C/G]GTAAAGGCTTTAACC | 235627 |
rs245196688 | in-del | -/GT | | | intron-variant | Nbeal2 | Mm_Celera | 9:110651099 | TCAGCTCCCCCATCA[-/GT]GTGTGTGTGTGTGTG | 235627 |
rs245341644 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110646323 | AGCATGCATGTGTGC[A/G]TGCATGGGTGTGTGT | 235627 |
rs245466898 | snp | G/T | | | upstream-variant-2KB, utr-variant-3-prime | Nradd, Nbeal2 | Mm_Celera | 9:110624901 | ACGTGGGATTTGAAA[G/T]TAGGGATTCCCTCCC | 235627 |
rs245512207 | snp | A/G | | | missense, downstream-variant-500B | Nbeal2, Mir8107 | Mm_Celera | 9:110635959 | CCGCCATCAGCAGCC[A/G]CCTGCTCCATCAGCA | 235627 |
rs245543687 | in-del | -/A | | | intron-variant | Nbeal2 | Mm_Celera | 9:110652612 | TTGAGCTCCATACCT[-/A]AAGCCTTCTGGGAGG | 235627 |
rs245548864 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nbeal2, Mir8107 | GRCm38.p3 | 9:110637174 | TGGAGAGAAAAGGCC[A/G]AACCTTTAGACCTTA | 235627 |
rs245577862 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110646920 | CACCATCAGCACCAC[C/T]ATCCGGCTTTAGTGG | 235627 |
rs245614252 | snp | C/T | | | upstream-variant-2KB, synonymous-codon | Nradd, Nbeal2 | Mm_Celera | 9:110625425 | AGACACACTGTGGAC[C/T]GGCACTTTCATGGGC | 235627 |
rs246026818 | in-del | -/CC | | | intron-variant | Nbeal2 | Mm_Celera | 9:110645022 | CTCTAAGTGCTGCTG[-/CC]CCATCTACCATTCAT | 235627 |
rs246141920 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110644756 | AGGATGAGAGGGTAG[A/G]GAATCCCACTGAAGA | 235627 |
rs246189062 | snp | C/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110633446 | GGGCTGGAGAAGTGG[C/T]TCAGCAGCTAAGAGC | 235627 |
rs246217283 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110643638 | AAGGAGTCCCTGTCT[A/G]GTGATGGGATTAGGC | 235627 |
rs246333340 | in-del | -/AACT | | | intron-variant | Nbeal2 | Mm_Celera | 9:110653645 | TGTGAAAAGGGTGAG[-/AACT]GACTGGCCAGGGCAA | 235627 |
rs246415661 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110640893 | TGTAGTCCTCTTCCA[C/T]CAGGTGCTGGGCCAG | 235627 |
rs246482551 | snp | G/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110650097 | GTCATTAAAGTTCCC[G/T]CCTCCTTCAATTACC | 235627 |
rs246566142 | snp | A/G | | | synonymous-codon | Nbeal2 | Mm_Celera | 9:110630206 | TTCCTCTGTTTCCAC[A/G]CGTTCCGTACTGCCG | 235627 |
rs246578346 | snp | A/C | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110630736 | CGCAGACTCAGCCCC[A/C]GCTGCACAGAAGGCA | 235627 |
rs246613488 | snp | A/G | | | synonymous-codon | Nbeal2 | Mm_Celera | 9:110632158 | GCGGGTCGGCACTGC[A/G]GTCTGCAGCAGTGTG | 235627 |
rs246632426 | in-del | -/GG | | | intron-variant | Nbeal2 | Mm_Celera | 9:110646329 | CATGTGTGCATGCAT[-/GG]GTGTGTGTGGGGGGG | 235627 |
rs247016052 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110633163 | GGGGTTTGCTGTGGG[A/G]ACAGGAAGGTGGTGT | 235627 |
rs247043361 | in-del | -/GT | | | intron-variant | Nbeal2 | Mm_Celera | 9:110642675 | TTATGTCCAAAAAGG[-/GT]AGGGCTTCCCAGAGT | 235627 |
rs247069045 | in-del | -/G | | | upstream-variant-2KB, downstream-variant-500B | Nradd, Nbeal2 | Mm_Celera | 9:110624537 | CACGCAGAAGCACTC[-/G]GGAGTTCACAGAAGC | 235627 |
rs247303775 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110627544 | GTAGACACAGAAGAC[A/G]CCAGGGTCGAGCCCG | 235627 |
rs247336622 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110628329 | GGAAGCGGCAGTCAA[C/T]GCAGGGACTGAATCC | 235627 |
rs247387696 | snp | G/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110653096 | GAGGGCCAGGGTAGA[G/T]CATGAACTCTCCCCA | 235627 |
rs247390029 | snp | A/G | | | upstream-variant-2KB | Ccdc12, Nbeal2 | Mm_Celera | 9:110655935 | AACAACTCATCAGGC[A/G]AGTGAGTGCAAGCTG | 235627 |
rs247584525 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110645223 | CCCACCCTTGCCCTG[A/G]AACCTCTACCCACGT | 235627 |
rs247699469 | snp | C/T | | | upstream-variant-2KB, synonymous-codon | Nradd, Nbeal2 | Mm_Celera | 9:110626283 | CACTGCAGCTACATG[C/T]CCGTATAAGACCTGC | 235627 |
rs247731406 | snp | G/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110627233 | GGGCGGAGGCAGAAG[G/T]GATGAAGCTAATGGG | 235627 |
rs247906645 | snp | A/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110649800 | TGAGCAGAGTGGTGT[A/T]AGTGCCTGGGTGTCC | 235627 |
rs248084238 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110647437 | AGGAAACCTAAGCTG[A/G]CCATCTGACCCTGAC | 235627 |
rs248462752 | snp | G/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110634316 | AAAGGCAAAAGGAGC[G/T]CCAGGGAGCAGAAGC | 235627 |
rs248621868 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110648960 | TATGTGCTGGCCCTC[A/G]TCTCCAGTCCAAGGG | 235627 |
rs248670819 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110627004 | CTGCAGCTGGCCTGT[A/G]TTCTGTTTAAATGGG | 235627 |
rs248978267 | snp | C/G | | | upstream-variant-2KB | Nbeal2 | Mm_Celera | 9:110654350 | TATTTCCATCCTCCC[C/G]AGTGAGGGGCCCGTA | 235627 |
rs249051144 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110639456 | TTGCACTCCCTTCGG[C/T]TGCGGAACACCTTCG | 235627 |
rs249093110 | snp | C/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110652604 | CCAGCCAGCTTGAGC[C/T]CCATACCTAAGCCTT | 235627 |
rs249243534 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110645095 | CTGTCCCACCACCTT[C/T]GCCTAGTTCTGCAGC | 235627 |
rs249255769 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110651212 | CCAGGTGCTGTCCCC[A/G]TCTCCTGGTCCTCTT | 235627 |
rs249457197 | snp | C/T | | | missense | Nbeal2 | Mm_Celera | 9:110626753 | TGTCGGCTTAGCTGA[C/T]TCAACAGCCTGCCAC | 235627 |
rs249483798 | in-del | -/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110647538 | TCAGTCAGAATGCTT[-/G]TGCATAAGCATAGAG | 235627 |
rs249488188 | in-del | -/A | | | intron-variant | Nbeal2 | Mm_Celera | 9:110650353 | ACCAACCAAACCAAC[-/A]AAAAAACAAAACAAC | 235627 |
rs249496079 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110627601 | TTACTCCTTGGCCTC[A/G]GCGCAGTGACAGCAG | 235627 |
rs249754751 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110633372 | CTTCAGAGAGGAGAT[A/G]TTCACAAAGGCCTTA | 235627 |
rs249880749 | snp | A/C | | | intron-variant | Nbeal2 | Mm_Celera | 9:110649819 | GCCTGGGTGTCCAGG[A/C]CAGCCTCTGCCCCTT | 235627 |
rs249962274 | snp | C/T | | | upstream-variant-2KB | Ccdc12, Nbeal2 | Mm_Celera | 9:110654602 | GAAGGAATCATCAGT[C/T]GACTGCAGGACAAAC | 235627 |
rs250037880 | snp | G/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110644309 | CTAGGTTCCTGGGGG[G/T]GGGGGTGAAGAACAG | 235627 |
rs250166343 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110648819 | CCCAGTACAGAAAGC[C/T]TCAAGTGGCCATCAC | 235627 |
rs250429878 | snp | C/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110639594 | TTTCTCTACATGGCC[C/G]GGACCCAGGACACCC | 235627 |
rs250592580 | in-del | -/CTT | | | upstream-variant-2KB | Ccdc12, Nbeal2 | Mm_Celera | 9:110655362 | GCCGCAGTCAAACTC[-/CTT]CTTCTCCTTTTGTTT | 235627 |
rs250716659 | in-del | -/TGTGTGTGTGTG | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110634579 | ACTGCACCTGTCCTT[-/TGTGTGTGTGTG]TGTGTGTGTGTGTGT | 235627 |
rs250746846 | snp | C/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110646619 | CACCTGTTTGTTTCC[C/T]TTTCCAAGCCTTCCT | 235627 |
rs250892411 | in-del | -/AAGAAAGA | | | intron-variant | Nbeal2 | Mm_Celera | 9:110650129 | AGCAACAAAAGCAGG[-/AAGAAAGA]AAGAAAGAAATTCCA | 235627 |
rs251048640 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110627380 | AGAAATGCGTAAGGC[C/T]GACTGAAGTAGACAG | 235627 |
rs251100949 | snp | A/C | | | intron-variant | Nbeal2 | Mm_Celera | 9:110646427 | CTATCACTCTCCATA[A/C]GGCCTCTCAAGTCCC | 235627 |
rs251112149 | snp | A/C | | | intron-variant | Nbeal2 | Mm_Celera | 9:110647078 | GTCGTGTCTTGTCCC[A/C]GAGCACTTACAGCTG | 235627 |
rs251291072 | snp | A/C | | | intron-variant | Nbeal2 | Mm_Celera | 9:110645212 | TTGCACAACAGCCCA[A/C]CCTTGCCCTGAAACC | 235627 |
rs251319126 | snp | A/G | | | missense | Nbeal2 | Mm_Celera | 9:110633899 | CCCGAGCCAATGCTG[A/G]CCCGTTCCAAACCCA | 235627 |
rs251369948 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110645786 | TGTACATTGGTCCTT[C/T]CCCACATCTGGAGCC | 235627 |
rs251421768 | snp | C/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110644153 | GGGACAGAGAATAGA[C/G]GGAGGGTTAGGCAGC | 235627 |
rs251427941 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110629715 | GTTGTCCAGAGCCCC[C/T]TATCTACAAAGTCTT | 235627 |
rs251528500 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110634935 | GGAGGGGCCACTGCA[C/T]GGGTGTGTGGCTCCA | 235627 |
rs251828900 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110648570 | GTCATTGCCCTAACC[C/T]GTCCCCAACCAGCCC | 235627 |
rs252108188 | in-del | -/A | | | intron-variant | Nbeal2 | Mm_Celera | 9:110645823 | GGGACACCAGAGAGC[-/A]AATCACCTTTCCCAG | 235627 |
rs252217416 | in-del | -/CTC | | | intron-variant | Nbeal2 | Mm_Celera | 9:110634671 | GGCAGGCATTCTGAT[-/CTC]CTCCGTCTGATCTGC | 235627 |
rs252310715 | snp | C/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110641579 | TGGGGTTCTGCACCA[C/G]TGGGAAACAGTCCTA | 235627 |
rs252311858 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110652249 | CTCAGACATTTGGCA[A/G]TCCTCCTGCCTCAAC | 235627 |
rs252322107 | snp | C/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110642912 | GAAACCTGGAGGGCA[C/G]AAGGGTCCAGGTCTG | 235627 |
rs252384607 | in-del | -/C | | | intron-variant, upstream-variant-2KB | Nbeal2, Mir8107 | Mm_Celera | 9:110636750 | TCCTGGGACAGGGGG[-/C]CAGTGGTGAATGAGA | 235627 |
rs252389732 | snp | A/G | | | synonymous-codon | Nbeal2 | Mm_Celera | 9:110628480 | CCTTCTCGTTGGTCA[A/G]CTGGAGGCAGCCCAG | 235627 |
rs252436944 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110651189 | TAACCTTCCCAAGTG[C/T]CAGCATGCCAGGTGC | 235627 |
rs252714274 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110629470 | GTCAGAGACCAAGAG[A/G]CCACATCTTAGTCGC | 235627 |
rs252772006 | in-del | -/C | | | intron-variant | Nbeal2 | Mm_Celera | 9:110651442 | AAAGGTGAAGAGGGG[-/C]GGTGTCAGAATGAGA | 235627 |
rs252882676 | snp | A/C | | | upstream-variant-2KB, intron-variant | Nradd, Nbeal2 | Mm_Celera | 9:110625519 | AAGGAAGCCAGCTAA[A/C]AGACACCTTTTCGTG | 235627 |
rs252903395 | snp | A/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110640524 | AATCAGCGAGGACAC[A/T]GTGTCTCAGCTTAGC | 235627 |
rs253293194 | in-del | -/CAC | | | intron-variant | Nbeal2 | Mm_Celera | 9:110646892 | TGCTACCACCATCAT[-/CAC]CACCACCACCACCAC | 235627 |
rs253476066 | snp | A/C | | | intron-variant, upstream-variant-2KB | Nbeal2, Mir8107 | GRCm38.p3 | 9:110636500 | CTCAAGCACAATCCC[A/C]AGCACCATACCAAGA | 235627 |
rs253478328 | snp | A/C | | | upstream-variant-2KB, downstream-variant-500B | Nradd, Nbeal2 | Mm_Celera | 9:110624558 | TCACAGAAGCCGACA[A/C]CAGCGTGCCTGGCAG | 235627 |
rs253499766 | snp | A/G | | | synonymous-codon, upstream-variant-2KB | Nbeal2, Mir8107 | GRCm38.p3 | 9:110637497 | GAGGGTAGAGCTGAC[A/G]CTGCCCTCCTGCAGA | 235627 |
rs253508804 | snp | C/T | | | upstream-variant-2KB, utr-variant-3-prime | Nradd, Nbeal2 | Mm_Celera | 9:110625058 | GCCCACCCCCTGGTG[C/T]AGTAGTCTCCTGGGC | 235627 |
rs253601013 | snp | C/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110643411 | GGAGGGGGGGTAGAG[C/T]CTGGGTAGAGACTAC | 235627 |
rs253622196 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110650656 | CACAGTGATCAGAAA[A/G]CAGAGACAGGCAGAT | 235627 |
rs253731266 | snp | C/T | | | missense | Nbeal2 | Mm_Celera | 9:110626628 | CAAGGCAGGTCACTA[C/T]ATCTGCATAGGAAGG | 235627 |
rs253765561 | in-del | -/GA | | | intron-variant | Nbeal2 | Mm_Celera | 9:110628830 | TAAGAAGCTGCCAGG[-/GA]GAGACTGTGTGCCTT | 235627 |
rs254092463 | snp | C/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110632243 | GTACCAATTGCTGGA[C/G]CCCCACCAGCTAGAC | 235627 |
rs254136033 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110627251 | TGAAGCTAATGGGAA[C/T]CTGCCAGGTGTACTT | 235627 |
rs254197374 | snp | G/T | | | upstream-variant-2KB | Ccdc12, Nbeal2 | Mm_Celera | 9:110656044 | GTGTTTGTCTGGTAG[G/T]GGTGCGTTAAGACAA | 235627 |
rs254461819 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110645864 | AGCCCAGAACTACAC[C/T]GAGAAGGAGATGAGA | 235627 |
rs254475517 | snp | G/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110650410 | AATCTGACTAAGCCG[G/T]TAAAGCCCCCTGCAC | 235627 |
rs254527019 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110651389 | TTGTTCTGGAACTCA[C/T]AAGAGATCTGACTGC | 235627 |
rs254584312 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110634678 | ATTCTGATCTCCTCC[A/G]TCTGATCTGCCTCTT | 235627 |
rs254685516 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110631174 | AGCAAAACGTTACAG[A/G]GCCCCCACTTTAAGA | 235627 |
rs254725907 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110632692 | CCCTCAGGTTATAAG[A/G]ACGCAGAATGTGTGT | 235627 |
rs254785678 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110647673 | ACCCAGCCAAGTTTA[C/T]AGGCTTTAGGTGTAG | 235627 |
rs255026543 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nbeal2, Mir8107 | GRCm38.p3 | 9:110637259 | GACAGGTTCCCAGGG[A/G]TGCCATCTTCCCTGG | 235627 |
rs255178361 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110648075 | GAGTCAGGTTCAGGG[C/T]TAGGCCAATCAAGGC | 235627 |
rs255337712 | snp | C/G | | | missense, upstream-variant-2KB | Nbeal2, Mir8107 | Mm_Celera | 9:110637379 | CCAGGCTACACAGGA[C/G]CCTTAGGGCAGATGG | 235627 |
rs255362619 | in-del | -/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110643829 | GGGGTGGGGAGAGTT[-/G]GGGGTGAAGCCGGGC | 235627 |
rs255604892 | in-del | -/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110643552 | CAGCCTAGGACAATA[-/T]GACTTTGCCCAAGCC | 235627 |
rs255658388 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110646892 | ATGCTACCACCATCA[C/T]CACCACCACCACCAC | 235627 |
rs255723019 | snp | A/C | | | intron-variant | Nbeal2 | Mm_Celera | 9:110647590 | CCACATAATCAGAAA[A/C]AGCAGCGCTTGTTCT | 235627 |
rs255749059 | snp | A/G | | | synonymous-codon | Nbeal2 | Mm_Celera | 9:110628227 | ATTGAGGGCCTCCTC[A/G]GCCGCTGGACCCCGC | 235627 |
rs255762589 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110639959 | GCCAGGTACACCACG[A/G]TCCAGGGCATCTGCT | 235627 |
rs255913904 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nbeal2, Mir8107 | Mm_Celera | 9:110637830 | TCCAGGTCACACTGG[C/T]CCAAGCCCCTCCAAC | 235627 |
rs255966328 | snp | A/C | | | upstream-variant-2KB, intron-variant | Nradd, Nbeal2 | Mm_Celera | 9:110625286 | CCGCACCCCACAACC[A/C]GCCACCCTCCTGCCC | 235627 |
rs255986077 | snp | A/G | | | synonymous-codon | Nbeal2 | Mm_Celera | 9:110630804 | CTCCAGTGCAGCCAG[A/G]TCCTCTTCCCCTAAC | 235627 |
rs256402516 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110649002 | CTGTTCCCATCCCAC[A/G]AGGCTGCACACACTT | 235627 |
rs256463392 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110630546 | GCTCACCCCTCCCTC[C/T]GCCCTGCTTCTCCTC | 235627 |
rs256564311 | snp | G/T | | | missense | Nbeal2 | GRCm38.p3 | 9:110633722 | TCATCCCCACTGATG[G/T]TGGGTTCTAGCAGGC | 235627 |
rs256612091 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110653476 | GTCTGAAGTGACGAA[C/T]GTCTGATGTACTTGT | 235627 |
rs257107277 | snp | A/C | | | intron-variant | Nbeal2 | Mm_Celera | 9:110643169 | CTGACTTGCTAAATG[A/C]TCCAAAAGGATCCGC | 235627 |
rs257152265 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | Nradd, Nbeal2 | Mm_Celera | 9:110624595 | CCACTGGCATGCAAA[C/T]GCCATGCAATGGACC | 235627 |
rs257187827 | snp | C/T | | | upstream-variant-2KB | Ccdc12, Nbeal2 | Mm_Celera | 9:110655017 | GGTCCAGATGGCTCC[C/T]ATTGGTCCTAGGGAT | 235627 |
rs257202753 | in-del | -/A | | | intron-variant | Nbeal2 | Mm_Celera | 9:110639498 | TAGGTCACAGTGCAG[-/A]AAAGAACAAGGACAA | 235627 |
rs257211668 | snp | A/G | | | synonymous-codon, upstream-variant-2KB | Nbeal2, Mir8107 | GRCm38.p3 | 9:110636307 | CACCTTGCGCAGGAG[A/G]GCCCCTATGATGGCA | 235627 |
rs257244227 | snp | G/T | | | upstream-variant-2KB | Ccdc12, Nbeal2 | Mm_Celera | 9:110655883 | CCTCGAACTCAGCAG[G/T]TCTGGAGCCAGAGAG | 235627 |
rs257245710 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110644578 | GAGATGCTGAGTGCC[A/G]AAGGGCAGTCCTACC | 235627 |
rs257293490 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110633194 | GGGCTGCGGGCTGTG[A/G]GGGAGGGGAATCTCT | 235627 |
rs257453807 | in-del | -/AAAA | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110645351 | TGGTGTGAACAACAG[-/AAAA]AAAAAAAAAAAAAAC | 235627 |
rs257472951 | snp | A/G | | | synonymous-codon | Nbeal2 | Mm_Celera | 9:110632074 | ATGCTCAGTCTCGGA[A/G]GACGAGGTGGTCAGC | 235627 |
rs257547500 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110645689 | CACCCACCTGGTTTC[C/T]GCAGGTCTTTTGCTT | 235627 |
rs257750185 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110640304 | CACACTGCCTCTGCA[C/T]CCTTCCTGTTCTCTG | 235627 |
rs257798417 | snp | G/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110627613 | CTCGGCGCAGTGACA[G/T]CAGGAAAGGGGAGCA | 235627 |
rs257961980 | in-del | -/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110629686 | CGGCACAATAGCAAA[-/G]GGTGAGCATTGAAGT | 235627 |
rs258001397 | in-del | -/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110640813 | CTGGGCAATAAGCAC[-/G]GGAGGCTGCCTTTTG | 235627 |
rs258144276 | snp | A/G | | | synonymous-codon | Nbeal2 | Mm_Celera | 9:110630221 | GCGTTCCGTACTGCC[A/G]TCATAGAAATACACG | 235627 |
rs258159569 | in-del | -/AAGA | | | intron-variant | Nbeal2 | Mm_Celera | 9:110650130 | AGCAACAAAAGCAGG[-/AAGA]AAGAAATTCCAATTG | 235627 |
rs258358985 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nbeal2, Mir8107 | GRCm38.p3 | 9:110637188 | CAAACCTTTAGACCT[C/T]AGGTCTTCTGGCCAA | 235627 |
rs258364113 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110649111 | GGTAGGGATTATTAA[C/T]TACTAGTGGAATTGG | 235627 |
rs258418926 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nbeal2, Mir8107 | GRCm38.p3 | 9:110638046 | CATGTTTGACTCTCC[A/G]TGCTCTCACCCCACC | 235627 |
rs258423678 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110639198 | ACGGGTAAGCCACAG[C/T]ACACATTGCACTGGC | 235627 |
rs258423717 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110650080 | TCTATGCTAATTTTT[C/T]TGTCATTAAAGTTCC | 235627 |
rs258439366 | snp | A/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110649195 | TTGTTAACCTAACAT[A/T]AAACTCTCTGAGCCT | 235627 |
rs258587577 | snp | C/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110627758 | ATGGGTAAGGACGTG[C/T]GGCTAAACCCATCTT | 235627 |
rs258723511 | snp | C/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110640147 | TCACAACTCACACTG[C/T]GCTGGCCACAGTTAA | 235627 |
rs258773164 | snp | G/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110627049 | TGTAGGACATTCATA[G/T]CGCACCCCTACCCGC | 235627 |
rs258821049 | in-del | -/TGG | | | intron-variant | Nbeal2 | Mm_Celera | 9:110649610 | CCTCCAGGTCTGGAC[-/TGG]AGGAAGAACTGGAGT | 235627 |
rs258846342 | snp | G/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110651900 | CAAGAGGACCCTGAG[G/T]CACACCAACTGATTT | 235627 |
rs258848693 | snp | C/T | | | upstream-variant-2KB | Ccdc12, Nbeal2 | Mm_Celera | 9:110655560 | GAGGAGAGAGTAATT[C/T]AGTGGCACTTATTCG | 235627 |
rs259196410 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110642577 | ATGTGGGGCAGAATG[C/T]CATGGCTGTACGCTA | 235627 |
rs259498393 | snp | A/G | | | upstream-variant-2KB | Ccdc12, Nbeal2 | Mm_Celera | 9:110655171 | CCAGGTTAACCCAGG[A/G]TAACACCGAGCTTAG | 235627 |
rs259551792 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110645784 | CCTGTACATTGGTCC[C/T]TCCCCACATCTGGAG | 235627 |
rs259595513 | snp | A/G | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110634302 | GTGCCCCACCCCAGA[A/G]AGGCAAAAGGAGCTC | 235627 |
rs259613131 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110646513 | CATGTTCCACTTTCC[A/G]TGGGTTCTCAGGAGC | 235627 |
rs259722097 | snp | A/G | | | synonymous-codon | Nbeal2 | GRCm38.p3 | 9:110632185 | TGTGTGCAGCTTCAC[A/G]TAGGCCTGGGCATGC | 235627 |
rs259736767 | snp | A/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110633304 | TTAGGAAAATGGCCT[A/T]AGGGTTTCAGCCACT | 235627 |
rs259761630 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110648927 | TCAACGACCCCCTCC[A/G]ACATTTGAGGCCCTG | 235627 |
rs259939433 | snp | C/G | | | intron-variant, downstream-variant-500B | Nbeal2, Mir8107 | Mm_Celera | 9:110635607 | CGCCAGGGCCCGCCA[C/G]CCTAACCTGTAGTGC | 235627 |
rs260102036 | snp | G/T | | | upstream-variant-2KB | Ccdc12, Nbeal2 | Mm_Celera | 9:110656050 | GTCTGGTAGTGGTGC[G/T]TTAAGACAAGGTTAT | 235627 |
rs260183200 | in-del | -/GATACCAGCG | | | intron-variant | Nbeal2 | Mm_Celera | 9:110653317 | CTTCGCTCCCCTTCT[-/GATACCAGCG]GAGTCAGCCTGAAAC | 235627 |
rs260298054 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110651285 | TCTACCCATTCACCA[C/T]GGCAGCTCTGTCCTG | 235627 |
rs260481553 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110643701 | CTGGGGAAATCAGGG[C/T]GGAGCCTAACCTTGG | 235627 |
rs260695625 | snp | A/C | | | intron-variant | Nbeal2 | Mm_Celera | 9:110629348 | GTAGAGCCTGTTCAC[A/C]ATACTACTTGGAAGG | 235627 |
rs260787108 | snp | C/T | | | synonymous-codon | Nbeal2 | Mm_Celera | 9:110638424 | CCACCGCTGCACGGG[C/T]GGCACCATGATGCCA | 235627 |
rs260966148 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110630408 | TTCTTGCCAAGCTCC[A/G]AGACCAGTGAGCCAT | 235627 |
rs261050248 | snp | G/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110646344 | GGGTGTGTGTGGGGG[G/T]GTGCATGCTTGCATG | 235627 |
rs261242218 | snp | C/T | | | intron-variant, downstream-variant-500B | Nbeal2, Mir8107 | Mm_Celera | 9:110635780 | TCTGCCCTCTATGTC[C/T]TCTCAGATTATAGAG | 235627 |
rs261281597 | snp | C/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110630140 | TCCCAGCCCAGCCTG[C/G]ACTTTGGTCATTCTC | 235627 |
rs261347331 | snp | C/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110646653 | AATCGCCTTCCCCAA[C/T]CACCAGGAGACCAAG | 235627 |
rs261508958 | in-del | -/GGGGT | | | intron-variant | Nbeal2 | Mm_Celera | 9:110635497 | AGGAGAGGTAAAATC[-/GGGGT]GGGGTGGGGTGGGAT | 235627 |
rs261572102 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110648584 | CCGTCCCCAACCAGC[C/T]CCAAATATACTCTAA | 235627 |
rs261609572 | snp | A/C | | | intron-variant | Nbeal2 | Mm_Celera | 9:110643978 | CCCCCTGGCCTCCTG[A/C]GGGTCACCCTGTCTG | 235627 |
rs261744724 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nbeal2, Mir8107 | GRCm38.p3 | 9:110638068 | CACCCCACCCTGGGC[C/T]ACATGAGAAGGACGG | 235627 |
rs261808957 | snp | C/G | | | synonymous-codon | Nbeal2 | Mm_Celera | 9:110628907 | CTGGACATGCAGGGA[C/G]GTGAAGGGCTCCACG | 235627 |
rs261955219 | snp | A/G | | | intron-variant, downstream-variant-500B | Nbeal2, Mir8107 | Mm_Celera | 9:110635511 | TCGGGGTGGGGTGGG[A/G]TGGGGAAACAGGCAG | 235627 |
rs261975875 | snp | A/G | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110643064 | ATCTAGATGGTTCTA[A/G]GAGTGCCTAGGCTGT | 235627 |
rs261992713 | snp | A/G | | | missense | Nbeal2 | Mm_Celera | 9:110631408 | CAGTGGAGCAGTGCC[A/G]TCGAGTGCTGCGCTG | 235627 |
rs262078510 | snp | C/T | | | upstream-variant-2KB, intron-variant | Nradd, Nbeal2 | Mm_Celera | 9:110626384 | AATGAAGATTTTATG[C/T]GAGCCAGAGGGTTGG | 235627 |
rs262101467 | in-del | -/CGCAATCACCATCACCACCG | | | intron-variant | Nbeal2 | Mm_Celera | 9:110648843 | CCATCACCATCACCA[-/CGCAATCACCATCACCACCG]CGCAATCAGTCAGTC | 235627 |
rs262298124 | snp | A/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110634233 | AAATAAGAGGTCATC[A/T]GACTGCTTCCCTAGA | 235627 |
rs262380920 | snp | C/T | | | synonymous-codon | Nbeal2 | Mm_Celera | 9:110628409 | CAGAGCCTGGCGGTG[C/T]TTCTGGATGAAATCC | 235627 |
rs262605705 | snp | G/T | | | upstream-variant-2KB, synonymous-codon | Nradd, Nbeal2 | Mm_Celera | 9:110625455 | CAGGGGAGGCACGGC[G/T]GGCCGCAATCTGGAG | 235627 |
rs262688759 | snp | A/G | | | synonymous-codon, upstream-variant-2KB | Nbeal2, Mir8107 | Mm_Celera | 9:110637105 | GAGGAGCAACTTGGT[A/G]CCAAACTCATGTAGT | 235627 |
rs262749940 | snp | G/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110630940 | GGAGGCCAATGGGAC[G/T]TAATTAGAGCAAGGC | 235627 |
rs262842854 | snp | A/G | | | upstream-variant-2KB | Nbeal2 | Mm_Celera | 9:110654401 | GAACCTATCGGGCTT[A/G]GAATTATCGCTGTTC | 235627 |
rs262984005 | snp | C/T | | | synonymous-codon | Nbeal2 | Mm_Celera | 9:110628230 | GAGGGCCTCCTCGGC[C/T]GCTGGACCCCGCTGC | 235627 |
rs263094576 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110652928 | CTGAGGGTAAAACTG[C/T]GTTGATTCTACAGCC | 235627 |
rs263271245 | snp | C/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110647809 | GTGAGGGAGTCAGAT[C/G]CCGGATCTGTGTTTC | 235627 |
rs263477562 | snp | A/T | | | upstream-variant-2KB | Ccdc12, Nbeal2 | Mm_Celera | 9:110655959 | CAAGCTGCCACTGGC[A/T]CTCTGTAGAGAAGGG | 235627 |
rs263667774 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110649749 | GCCATGGGATGGAGC[C/T]GGAACATTCAACCTG | 235627 |
rs263803824 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110652304 | ATGTGCCATCATGCT[A/G]GGGCGAAGGGTCTCG | 235627 |
rs263844616 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110647640 | CAGAGGCAGGCAGGT[C/T]GGTGGAGCTCAAAGG | 235627 |
rs263998677 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110643030 | ACCACTGGAGGGTCC[C/T]ACAAATGGGTGGGAA | 235627 |
rs264070961 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110641916 | TCCCCTACAGGTACC[C/T]TTAAACAGCCCGCCT | 235627 |
rs264102624 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110649373 | CACCTGCCCAAGGGT[A/G]GGATGACAGGGAGCT | 235627 |
rs264125553 | snp | C/G | | | upstream-variant-2KB | Ccdc12, Nbeal2 | Mm_Celera | 9:110655745 | GATTAAAGGCGTGCG[C/G]CACCACGCCCGGCTG | 235627 |
rs264159370 | snp | A/G | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110645371 | AAAAAAAAAAAAACC[A/G]TTTCCTTTGCCCTTG | 235627 |
rs264212718 | snp | C/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110647557 | ATAAGCATAGAGACC[C/G]GAACTTCCATCCCAG | 235627 |
rs264269846 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nbeal2, Mir8107 | Mm_Celera | 9:110636181 | AGGCAGGCAGGGCTA[C/T]GGCCCAACTTCTTCT | 235627 |
rs264440455 | snp | C/T | | | upstream-variant-2KB | Ccdc12, Nbeal2 | Mm_Celera | 9:110654675 | TACAGTAGCCCACTC[C/T]CTCTAGGAATCCTGC | 235627 |
rs264479816 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110647471 | TGCCTCAGTGGCCTC[A/G]TAGACCCTTTCTGGT | 235627 |
rs264721455 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110638934 | AGAATGTGACAATCC[C/T]GGTCACTGGTGGCCC | 235627 |
rs264730394 | snp | A/G | | | synonymous-codon | Nbeal2 | Mm_Celera | 9:110628019 | ACAAGGAGTCTGCCC[A/G]AAGTTGCTGATGATG | 235627 |
rs264876837 | snp | A/G | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110630434 | GCCATGAGGTCACAT[A/G]CTCATATCTCCCTGA | 235627 |
rs265203206 | snp | C/T | | | missense | Nbeal2 | Mm_Celera | 9:110626867 | TGTGCACTCACGCCA[C/T]TGTCTGAGACCCAGG | 235627 |
rs265356852 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110629032 | ATCTGAAGCCACAGG[C/T]AGCACATGTCAGCAG | 235627 |
rs265509655 | snp | A/G | | | intron-variant | Nbeal2 | Mm_Celera | 9:110651767 | GTGAAGGTTAAAAAC[A/G]CTCCAAGAGGAACAA | 235627 |
rs265651588 | snp | C/T | | | upstream-variant-2KB | Ccdc12, Nbeal2 | Mm_Celera | 9:110655127 | GCAGCCACCCCGTCT[C/T]CTACTGTAAGGGAAG | 235627 |
rs265775692 | snp | A/C | | | intron-variant | Nbeal2 | Mm_Celera | 9:110648519 | AGGAAGTACTTGGAC[A/C]TTGCTACAGGGGAGA | 235627 |
rs265984159 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110650102 | TAAAGTTCCCTCCTC[C/T]TTCAATTACCTTAGC | 235627 |
rs266124138 | in-del | -/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110646837 | AGATTCACCTGTTTC[-/T]TGCCTCCCAAGTCTA | 235627 |
rs266209890 | snp | G/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110652831 | CCTTGAAGATGGAGA[G/T]ACAGGGGCTGAATGG | 235627 |
rs266219370 | snp | C/T | | | intron-variant | Nbeal2 | Mm_Celera | 9:110645947 | CCTCACACCTAAGGA[C/T]CCCCAGAACCTTATG | 235627 |
rs386862092 | in-del | -/TG | | | intron-variant | Nbeal2 | Mm_Celera | 9:110651114 | GTGTGTGTGTGTGTG[-/TG]CACGTGCGTGCACTG | 235627 |
rs387211226 | in-del | -/TCT | | | upstream-variant-2KB | Ccdc12, Nbeal2 | Mm_Celera | 9:110655367 | AGTCAAACTCCTTCT[-/TCT]CCTTTTGTTTTGTGA | 235627 |
rs387231021 | in-del | -/GAGA | | | intron-variant | Nbeal2 | Mm_Celera | 9:110644776 | CCACTGAAGAGGGGA[-/GAGA]AAGGTGGAGTTCTAG | 235627 |
rs387713879 | in-del | -/AAGCTCCAGCCACACC | | | intron-variant | Nbeal2 | Mm_Celera | 9:110647387 | AAAAGACTCAGCCCC[-/AAGCTCCAGCCACACC]TTTTGGGCTGAAGGC | 235627 |
rs578305812 | snp | G/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110640560 | TTGAGAGTCAGAGCA[G/T]ACTGCTCGCTCCCAC | 235627 |
rs578714860 | snp | C/T | | | upstream-variant-2KB | Ccdc12, Nbeal2 | GRCm38.p3 | 9:110655703 | TCGAACTCAGAAATC[C/T]GCCTGCCTCTGCCTC | 235627 |
rs579101546 | snp | G/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110643603 | CCCCTAGAGGTTCCC[G/T]TGTCTCAGGCCAGAC | 235627 |
rs579532686 | snp | C/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110646851 | CTTGCCTCCCAAGTC[C/T]AAGTGCTGGGATTAA | 235627 |
rs579743017 | snp | A/G | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110647801 | ATGTCTGTGTGAGGG[A/G]GTCAGATCCCGGATC | 235627 |
rs580410979 | snp | A/G | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110629755 | CCCCACACAAACAGG[A/G]TCTAGGATGCTTACC | 235627 |
rs580598699 | snp | A/G | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110645900 | CAGTCAGTGCTTACG[A/G]GCCGGGCCGAGACTG | 235627 |
rs580696519 | snp | A/T | | | upstream-variant-2KB | Ccdc12, Nbeal2 | GRCm38.p3 | 9:110654631 | ACCTACCTGCAGAGG[A/T]GCGGCGTCCTTACCA | 235627 |
rs581345208 | snp | A/G | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110630762 | AGGCATCCATCCCTG[A/G]CAGCCCCGGCCCACC | 235627 |
rs581538514 | snp | C/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110649862 | AAGAGGACCTAAAGG[C/T]CCCATAACACATAAC | 235627 |
rs582157447 | snp | A/G | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110642928 | AAGGGTCCAGGTCTG[A/G]GTCACATGGGGAGGA | 235627 |
rs582686590 | snp | C/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110646826 | CTCGAACTCAGAGAT[C/T]CACCTGTTTCTTGCC | 235627 |
rs583336009 | snp | C/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110647202 | CAGGTATAATACATA[C/T]GAGTAACAGAGCCAG | 235627 |
rs584094461 | snp | G/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110640545 | TCAGCTTAGCTGAGA[G/T]TGAGAGTCAGAGCAG | 235627 |
rs584225087 | snp | A/G | | | upstream-variant-2KB | Ccdc12, Nbeal2 | GRCm38.p3 | 9:110655632 | TGTTTTTCGAGACAG[A/G]GTTTCCCTGTATAGC | 235627 |
rs584468037 | snp | G/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110642959 | ACAGGAGGAACCGGA[G/T]AGGCATGGGGACAGG | 235627 |
rs585086175 | snp | G/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110651101 | CAGCTCCCCCATCAG[G/T]GTGTGTGTGTGTGCA | 235627 |
rs585246175 | snp | A/G | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110646848 | TTTCTTGCCTCCCAA[A/G]TCTAAGTGCTGGGAT | 235627 |
rs585951196 | snp | C/G | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110644389 | CCGTGCCTCTGGCCA[C/G]CCTGGGAGGACAGCA | 235627 |
rs586332318 | snp | C/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110651107 | CCCCATCAGTGTGTG[C/T]GTGTGTGCACGTGCG | 235627 |
rs587029760 | snp | C/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110647549 | GCTTGTGCATAAGCA[C/T]AGAGACCCGAACTTC | 235627 |
rs587267960 | snp | A/G | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110649691 | AGGAGAGAGGGCAAT[A/G]TCAGGCCATGGGTGG | 235627 |
rs587404808 | snp | C/T | | | intron-variant | Nbeal2 | GRCm38.p3 | 9:110630756 | CACAGAAGGCATCCA[C/T]CCCTGGCAGCCCCGG | 235627 |
rs587563408 | snp | C/G | | | intron-variant, upstream-variant-2KB | Nbeal2, Mir8107 | GRCm38.p3 | 9:110636743 | CACCACATCCTGGGA[C/G]AGGGGGCCAGTGGTG | 235627 |
rs864268439 | snp | C/T | | | missense | Nbeal2 | GRCm38.p3 | 9:110631874 | TGCTTGTCGATGAAG[C/T]GGCGCCATTCGGCTG | 235627 |
rs864271447 | snp | C/T | | | synonymous-codon | Nbeal2 | GRCm38.p3 | 9:110638556 | CTTCTGAGATTCATT[C/T]CCACTTGACTCTGAG | 235627 |