SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3088589 | snp | G/T | 0.21875 | 0.248039 | intron-variant | Nck2 | GRCm38.p3 | 1:43492133 | CAAGTGGGCAGCCAT[G/T]CGAGGCACCAGCTGA | 17974 |
rs3655419 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Nck2 | GRCm38.p3 | 1:43506408 | CTCTTTTATCTGAAG[A/G]CTCAGTGCCTTAATC | 17974 |
rs3662842 | snp | A/G | 0.5 | 0 | intron-variant | Nck2 | GRCm38.p3 | 1:43449466 | AAAAACAAAACCCAC[A/G]AAATTCCTTTATGTC | 17974 |
rs3664066 | snp | A/C | 0.5 | 0 | intron-variant | Nck2 | GRCm38.p3 | 1:43449691 | TGCAGGTGTGTGCCT[A/C]GCTGGAGTGTTGGAG | 17974 |
rs3703031 | snp | G/T | 0.471655 | 0.115624 | intron-variant | Nck2 | Mm_Celera | 1:43467508 | GTGTGATCAGCCGTA[G/T]TAGAACACACCCTGG | 17974 |
rs3703581 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nck2 | Mm_Celera | 1:43467580 | GGCAGGAGGATCAGG[A/G]ATTCAAGGCCAGCCT | 17974 |
rs3709917 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Nck2 | GRCm38.p3 | 1:43480337 | TTGGGGTCAGTCTCC[A/G]TCTGTTAGAAGGAAA | 17974 |
rs3724978 | snp | C/G | 0.5 | 0 | intron-variant | Nck2 | GRCm38.p3 | 1:43480429 | TAAAAAATACCTTAG[C/G]TAAACGGTTAGTCTT | 17974 |
rs3724989 | snp | C/T | 0.5 | 0 | intron-variant | Nck2 | GRCm38.p3 | 1:43480434 | AATACCTTAGCTAAA[C/T]GGTTAGTCTTGTCTG | 17974 |
rs4136282 | snp | A/C | 0.5 | 0 | intron-variant | Nck2 | GRCm38.p3 | 1:43449602 | GGGAATGGttttgtt[A/C]ttctgagacgtttcc | 17974 |
rs6185575 | snp | C/T | 0.5 | 0 | intron-variant | Nck2 | GRCm38.p3 | 1:43454608 | CTTCTGTTCTGACCA[C/T]CTCACCCTCTAAGCC | 17974 |
rs6187198 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Nck2 | Mm_Celera | 1:43454898 | ACACTGTTCTTCGGA[C/T]GACTCCCCTGCGCCC | 17974 |
rs6286954 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43472803 | AGTAGCCTATGGTAT[A/G]GACCNTGTCTTTGGA | 17974 |
rs6286960 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Nck2 | Mm_Celera | 1:43472808 | CCTATGGTATNGACC[A/G]TGTCTTTGGAATCCA | 17974 |
rs6287440 | snp | A/G | 0.5 | 0 | intron-variant | Nck2 | Mm_Celera | 1:43472845 | GGCAGCCTCAGATGG[A/G]AAAATCTNAGGACGN | 17974 |
rs6287459 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Nck2 | Mm_Celera | 1:43472853 | CAGATGGNAAAATCT[C/T]AGGACGNGGACAGTG | 17974 |
rs6287475 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Nck2 | Mm_Celera | 1:43472860 | NAAAATCTNAGGACG[C/T]GGACAGTGTAGTTAG | 17974 |
rs6288037 | snp | C/G | 0.5 | 0 | intron-variant | Nck2 | Mm_Celera | 1:43472975 | GTAGCATTAATCACC[C/G]TGAGTTAGGTATTGT | 17974 |
rs6288576 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Nck2 | Mm_Celera | 1:43473070 | TGGGCATTTTAGGAC[C/T]GTGCTCTGGTGGGAG | 17974 |
rs6288979 | snp | A/T | 0.290657 | 0.246672 | intron-variant | Nck2 | Mm_Celera | 1:43473119 | AGACGCCATGAAGGC[A/T]CTAAAGGATATCTGT | 17974 |
rs6289117 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Nck2 | Mm_Celera | 1:43473194 | GAAAGAAGTGTGGCC[C/T]AAGAAGATTTACATG | 17974 |
rs6289603 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Nck2 | Mm_Celera | 1:43473258 | TCATTACTACGTAGG[C/T]TCGTTTAGAAATAAA | 17974 |
rs6289649 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Nck2 | Mm_Celera | 1:43473283 | AATAAATACGCTGTC[A/G]TCTGGGTACTCATTT | 17974 |
rs6289680 | snp | C/G | 0.290657 | 0.246672 | intron-variant | Nck2 | Mm_Celera | 1:43473305 | TACTCATTTGGTTTT[C/G]TGAAAAACTTGGTTT | 17974 |
rs6290196 | snp | A/G | 0.5 | 0 | intron-variant | Nck2 | Mm_Celera | 1:43473384 | GTCTAACATTTATTC[A/G]TACGGGTGCGGCATG | 17974 |
rs6392281 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Nck2 | Mm_Celera | 1:43458130 | TTTGAATAAGCAGTG[C/T]TCACTTAGTGAGTAT | 17974 |
rs6392318 | snp | C/T | 0.5 | 0 | intron-variant | Nck2 | GRCm38.p3 | 1:43458153 | GTGAGTATTTATTGA[C/T]ACCAACTGTGTGCCA | 17974 |
rs6392865 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Nck2 | Mm_Celera | 1:43458238 | GAGATTTCTTTTAGT[C/T]CACACTCATTTCTGA | 17974 |
rs6392945 | snp | G/T | 0.359862 | 0.224567 | intron-variant | Nck2 | Mm_Celera | 1:43458278 | ACCATCTCCACATTT[G/T]CGTGAGAGGTGACAC | 17974 |
rs6393011 | snp | A/G | 0.5 | 0 | intron-variant | Nck2 | Mm_Celera | 1:43458301 | GGTGACACTACACAA[A/G]GTCTCTCCCACCCTC | 17974 |
rs6407146 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Nck2 | Mm_Celera | 1:43458514 | CAGACCATTTGTTTG[C/T]ACACAGTAGACTCTT | 17974 |
rs6407260 | snp | A/T | 0.5 | 0 | intron-variant | Nck2 | Mm_Celera | 1:43458590 | GCTTGTCTGTTGCTT[A/T]CTTANTTAAAAAAAA | 17974 |
rs6407263 | snp | C/T | 0.5 | 0 | intron-variant | Nck2 | Mm_Celera | 1:43458595 | TCTGTTGCTTNCTTA[C/T]TTAAAAAAAATCAGT | 17974 |
rs6407702 | snp | G/T | 0.304688 | 0.243945 | intron-variant | Nck2 | Mm_Celera | 1:43458632 | ACTTATTGAAGGTTT[G/T]AGCTGAATATTGCAT | 17974 |
rs6408261 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Nck2 | Mm_Celera | 1:43458735 | TTGTTTTTATGTATG[A/G]Attttgagataggnt | 17974 |
rs6408276 | snp | C/T | 0.5 | 0 | intron-variant | Nck2 | Mm_Celera | 1:43458749 | GNAttttgagatagg[C/T]tttcaggccctggct | 17974 |
rs13475311 | snp | G/T | | | synonymous-codon | Nck2 | Mm_Celera | 1:43554153 | AGCGGACGAAGCTGC[G/T]GCTGAGGCCCCCAGC | 17974 |
rs30510648 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Nck2 | Mm_Celera | 1:43463913 | TTATTTTATAATGTT[C/T]TGGCAGTTGGATTGG | 17974 |
rs30544951 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nck2 | GRCm38.p3 | 1:43455757 | TCTCCCTAGGATCTG[C/T]CTTGCTTGGCTTTAT | 17974 |
rs30559195 | snp | A/T | 0.32 | 0.24 | intron-variant | Nck2 | GRCm38.p3 | 1:43456779 | ATCAAAAGACATCAG[A/T]TTTCTTAGAAACTTT | 17974 |
rs30570519 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nck2 | GRCm38.p3 | 1:43452284 | CTTCTTTAATGTTGT[A/G]TCTGGATACATTTGG | 17974 |
rs30603448 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nck2 | GRCm38.p3 | 1:43507441 | GGAATGTGTGGAAAA[C/T]ACCAGCCCGAATCCA | 17974 |
rs30604338 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nck2 | GRCm38.p3 | 1:43483252 | TCTGCCACCCGCATC[C/T]CCTCGTGGGGCAGAC | 17974 |
rs30612578 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Nck2 | GRCm38.p3 | 1:43465759 | TATGTGGCACAGTCG[A/G]TTCCATGAGCATCAG | 17974 |
rs30654619 | snp | C/G/T | 0.375 | 0.216506 | intron-variant | Nck2 | GRCm38.p3 | 1:43507414 | ACCTATTAGAAATGT[C/G/T]GGGGGTTGGGGAATG | 17974 |
rs30665769 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Nck2 | GRCm38.p3 | 1:43474549 | CTCTATTCAGCTAGT[A/G]GTGGAGCAGGCTGCC | 17974 |
rs30668834 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Nck2 | GRCm38.p3 | 1:43483683 | ATAGATTGAAGATTT[G/T]CAGGGTAACACAAAA | 17974 |
rs30743927 | snp | C/G | 0.487535 | 0.077957 | intron-variant | Nck2 | GRCm38.p3 | 1:43461226 | GGAGGCGATAGGGTG[C/G]TTCTTCAGCATATTT | 17974 |
rs30759334 | snp | A/T | 0.456747 | 0.140554 | intron-variant | Nck2 | GRCm38.p3 | 1:43485740 | TATTCAGGCACAAGA[A/T]GGAAGACAAACCACA | 17974 |
rs30771005 | snp | C/G | 0.375 | 0.216506 | intron-variant | Nck2 | GRCm38.p3 | 1:43565451 | AGTTGCCGTATCTCA[C/G]GCAGCCTTGCAGAGG | 17974 |
rs30810517 | snp | C/T | 0.495 | 0.0497494 | intron-variant | Nck2 | GRCm38.p3 | 1:43482676 | ATTGGATGAGTATCT[C/T]TCAGAAGGAAACAAG | 17974 |
rs30849043 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nck2 | Mm_Celera | 1:43454739 | AAAAAAAAATCAATG[A/G]TAGGGAGTGGAGCTT | 17974 |
rs30851620 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Nck2 | GRCm38.p3 | 1:43500526 | ACCCAGCCCACATCC[G/T]AAACTGACTGTTGTA | 17974 |
rs30853989 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nck2 | GRCm38.p3 | 1:43483607 | ACCAGTGGAACTTTC[C/T]AGAAAGTGAAGCCCT | 17974 |
rs30859589 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nck2 | GRCm38.p3 | 1:43475565 | TTTTATAGCCTACCC[C/T]TTGGGGAGGGGCATC | 17974 |
rs30898871 | snp | C/G/T | 0.484429 | 0.0868505 | intron-variant | Nck2 | GRCm38.p3 | 1:43507727 | GTGCTGAGTTGTCTG[C/G/T]GCCAATTAGGTTGTA | 17974 |
rs30901766 | snp | A/C | 0.475309 | 0.108333 | intron-variant | Nck2 | GRCm38.p3 | 1:43505174 | ATAGTCTGTATGGGG[A/C]TGAACCTTTGAAAGG | 17974 |
rs30908704 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Nck2 | GRCm38.p3 | 1:43493051 | GGAAACTAAATGGTT[A/G]TGTATCAGCTGTGTG | 17974 |
rs30944904 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Nck2 | GRCm38.p3 | 1:43474659 | TTTGAAGTCATGCCA[C/T]AGCAACTCTTTGAGG | 17974 |
rs30953163 | snp | C/G | 0.32 | 0.24 | intron-variant | Nck2 | GRCm38.p3 | 1:43448678 | GTGCTGGGATTAAAG[C/G]CGTGCAACACCACGC | 17974 |
rs30990828 | snp | C/G | 0.375 | 0.216506 | intron-variant | Nck2 | GRCm38.p3 | 1:43502652 | CCAGTCAGCAGTACC[C/G]TTCTGTGGCCTGTGA | 17974 |
rs31007990 | snp | G/T | 0.197531 | 0.244432 | intron-variant | Nck2 | GRCm38.p3 | 1:43469371 | CTCCATCCTGCCCAC[G/T]GTCCTTGTGGACGGT | 17974 |
rs31009436 | snp | G/T | 0.375 | 0.216506 | upstream-variant-2KB | Nck2 | Mm_Celera | 1:43444187 | CCACTGTCATCACGG[G/T]GGGAAGCTTGGTAGC | 17974 |
rs31044463 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Nck2 | GRCm38.p3 | 1:43444338 | TCTCCTCCAACAAGG[A/G]CATACCCTCCTAATC | 17974 |
rs31056788 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Nck2 | GRCm38.p3 | 1:43459092 | GATCACAAAGGTGGT[C/T]TGTGAAACTTTTCTA | 17974 |
rs31130536 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | Nck2 | GRCm38.p3 | 1:43534537 | TGGTGTAAGTACAAT[A/C]TGGCAAGAGACTAGG | 17974 |
rs31158552 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Nck2 | GRCm38.p3 | 1:43461622 | GAGGGCAGAGCGTAT[G/T]GTGGGGGATGCTATC | 17974 |
rs31187945 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nck2 | GRCm38.p3 | 1:43499741 | TAGTTTTTTGTTTGT[C/T]TTGTTTTGTTGTTTT | 17974 |
rs31226928 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nck2 | GRCm38.p3 | 1:43500525 | AACCCAGCCCACATC[C/T]TAAACTGACTGTTGT | 17974 |
rs31235948 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nck2 | GRCm38.p3 | 1:43483314 | GTTCCCACAGTGGGC[A/G]CAGTAGCTGGTGGGA | 17974 |
rs31240477 | snp | A/T | 0.5 | 0 | intron-variant | Nck2 | Mm_Celera | 1:43503311 | GCAACCTAAAAGTTT[A/T]TTTTTTTTTAATAGA | 17974 |
rs31241631 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Nck2 | GRCm38.p3 | 1:43482814 | AAGGTGAAGAAACTA[A/G]AGCTATTTTAAAAGT | 17974 |
rs31286746 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Nck2 | GRCm38.p3 | 1:43467780 | CCCACAAGGCCAACA[A/C]ACTGTTTTTTTCGCT | 17974 |
rs31297530 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nck2 | GRCm38.p3 | 1:43467460 | CAGTGCTTCGCAAAC[A/G]GCCCCTGGACTGAAT | 17974 |
rs31305667 | snp | A/G | 0.495 | 0.0497494 | intron-variant | Nck2 | GRCm38.p3 | 1:43472197 | AAAGGCTTTCTTCTT[A/G]ACAAGCTTTCATTCC | 17974 |
rs31378057 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Nck2 | Mm_Celera | 1:43466939 | TTCCATCCACAAACC[C/T]TGTGTCTGTGTTTAG | 17974 |
rs31403525 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Nck2 | Mm_Celera | 1:43474887 | GAAAGTAAGAGAGCC[A/G]CCTATAGCTGGAGCT | 17974 |
rs31420911 | snp | C/G | 0.444444 | 0.157135 | upstream-variant-2KB | Nck2 | Mm_Celera | 1:43444910 | TTCTTTTTTTGTTAC[C/G]TAGGGTGAATTGTTT | 17974 |
rs31490848 | snp | A/G | 0.495 | 0.0497494 | intron-variant | Nck2 | GRCm38.p3 | 1:43468861 | AAGCAGTGGAGGCAA[A/G]ATCGAAAGACCCCCA | 17974 |
rs31527127 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nck2 | GRCm38.p3 | 1:43510213 | TCCCTAATTTACTGA[A/G]CTCCATTAAATTTAA | 17974 |
rs31549145 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nck2 | GRCm38.p3 | 1:43448850 | TCCCGCCCTTTCTTT[C/T]CCCTGGAGTTCACTT | 17974 |
rs31552064 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Nck2 | GRCm38.p3 | 1:43502913 | AGTTTACTTTCTAAC[C/T]CGGTTTTAAGCTCAG | 17974 |
rs31569915 | snp | A/C | 0.429688 | 0.173817 | intron-variant | Nck2 | GRCm38.p3 | 1:43482824 | AACTAAAGCTATTTT[A/C]AAAGTAGCCCAAGAT | 17974 |
rs31620260 | snp | C/G | 0.32 | 0.24 | intron-variant | Nck2 | GRCm38.p3 | 1:43448696 | TGCAACACCACGCCC[C/G]GCAATGCATTTCTTT | 17974 |
rs31622177 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nck2 | Mm_Celera | 1:43454435 | CCCCCCCCTCTACGC[A/G]AGACCAGACATTGTA | 17974 |
rs31652254 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Nck2 | GRCm38.p3 | 1:43487116 | ATATACTATTCCAGG[A/G]TCTATTGGACCAAAT | 17974 |
rs31676158 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nck2 | GRCm38.p3 | 1:43483381 | GTTTGTTCCTTTGAG[A/G]ATTATAAAATATGCA | 17974 |
rs31734176 | snp | G/T | 0.375 | 0.216506 | intron-variant | Nck2 | GRCm38.p3 | 1:43483933 | CTTCTGTAGAAGTAG[G/T]TTCCAACTGATGTGC | 17974 |
rs31767678 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nck2 | GRCm38.p3 | 1:43455758 | CTCCCTAGGATCTGC[C/T]TTGCTTGGCTTTATA | 17974 |
rs31835972 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Nck2 | GRCm38.p3 | 1:43466810 | AAGCCTGCTGTCCTT[C/T]AACTCCTTCCATGTG | 17974 |
rs31865475 | snp | A/G | 0.495 | 0.0497494 | intron-variant | Nck2 | GRCm38.p3 | 1:43458439 | GTAGCTGTGTACGTT[A/G]GTGGCTGCCTCAACA | 17974 |
rs31867299 | snp | G/T | 0.487535 | 0.077957 | intron-variant | Nck2 | GRCm38.p3 | 1:43456620 | ATCCGTGTCCAGTCA[G/T]CATACCTGTACCACA | 17974 |
rs31873204 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Nck2 | GRCm38.p3 | 1:43475442 | TTGGCACCTAGTAAC[A/G]CCATCACTGTCTGGC | 17974 |
rs31887674 | snp | C/G | 0.375 | 0.216506 | intron-variant | Nck2 | GRCm38.p3 | 1:43467453 | TGTAGAACAGTGCTT[C/G]GCAAACGGCCCCTGG | 17974 |
rs31894678 | snp | G/T | 0.49827 | 0.0293608 | intron-variant | Nck2 | GRCm38.p3 | 1:43503662 | GCCTCATGCAGGCCA[G/T]TCATTCTGTTCATAG | 17974 |
rs31902252 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Nck2 | GRCm38.p3 | 1:43565443 | GTTGAGTCAGTTGCC[A/G]TATCTCAGGCAGCCT | 17974 |
rs31919412 | snp | A/C/G | 0.32 | 0.24 | intron-variant | Nck2 | GRCm38.p3 | 1:43484123 | CCTCAGTCCCCTTTG[A/C/G]GAAATGCCAGCCTTA | 17974 |
rs31929637 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Nck2 | GRCm38.p3 | 1:43564916 | ATAATAATGAATTCT[A/G]TGACCCTGTTGTCTA | 17974 |
rs31955630 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Nck2 | GRCm38.p3 | 1:43485050 | GAACCATAATTCTTA[A/G]TAAGTGCTAGGTCTT | 17974 |
rs31985789 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Nck2 | GRCm38.p3 | 1:43467739 | TCGTGGTAGTGTAGT[A/G]GGATTGAGTAATTGT | 17974 |
rs31990396 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Nck2 | GRCm38.p3 | 1:43511289 | TTCATGAGGGTGTAG[C/T]TAATGAAGTGCCCTA | 17974 |
rs32026033 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Nck2 | GRCm38.p3 | 1:43444678 | GTACAGGATGCCTCC[C/T]AGTGCCCTCGTGTCA | 17974 |
rs32026247 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Nck2 | GRCm38.p3 | 1:43467131 | CTTTCATTAGATCCC[C/T]TTTACTTTAGTGGTG | 17974 |
rs32037891 | snp | A/T | 0.359862 | 0.224567 | intron-variant | Nck2 | GRCm38.p3 | 1:43483026 | AGGAAGTGATGCCCA[A/T]GTTCTGGCCATTGCC | 17974 |
rs32044299 | snp | A/G | 0.5 | 0 | intron-variant | Nck2 | GRCm38.p3 | 1:43564847 | CTGAGCCCAGTGCAA[A/G]GGTGTGAAATTAAAT | 17974 |
rs32050015 | snp | A/G | 0.495 | 0.0497494 | intron-variant | Nck2 | GRCm38.p3 | 1:43468649 | TACTGCTAGTTTGTT[A/G]GGGGACATGCAATTC | 17974 |
rs32056222 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nck2 | Mm_Celera | 1:43467210 | AGAGAAATGTATTAA[C/T]GTAACTTCCCATTCA | 17974 |
rs32068016 | snp | G/T | 0.5 | 0 | intron-variant | Nck2 | GRCm38.p3 | 1:43456678 | GTGACACCTATCTGA[G/T]CTGTGAATAAAGTCC | 17974 |
rs32090752 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Nck2 | GRCm38.p3 | 1:43489826 | CTATTTGTAGGACTG[A/G]AAGTGTTAAAAGTTG | 17974 |
rs32093360 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Nck2 | GRCm38.p3 | 1:43466680 | TTACTAGTTTTAATG[C/T]CTTCAAGTTAGTATA | 17974 |
rs32147763 | snp | G/T | 0.487535 | 0.077957 | intron-variant | Nck2 | GRCm38.p3 | 1:43458888 | TGTGGAACAGTGGGT[G/T]TTGCAGATCAACCCT | 17974 |
rs32159847 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nck2 | GRCm38.p3 | 1:43456324 | TCCTGTAATACATAA[A/G]CCTATCCCCACAGCC | 17974 |
rs32170516 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nck2 | GRCm38.p3 | 1:43455375 | GTATCAAGCCTGGGT[A/G]TGTGAGGAGGGCCAG | 17974 |
rs32194495 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nck2 | GRCm38.p3 | 1:43483380 | AGTTTGTTCCTTTGA[A/G]GATTATAAAATATGC | 17974 |
rs32205653 | snp | C/T | 0.455 | 0.143091 | intron-variant | Nck2 | GRCm38.p3 | 1:43463419 | CCCGCCTGAGGTGAC[C/T]TGTGACCATATCTCA | 17974 |
rs32219071 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Nck2 | GRCm38.p3 | 1:43455095 | TCTGGTGTTTGGAGG[C/T]TACTCGAGTCTTGGT | 17974 |
rs32225915 | snp | A/G | 0.42 | 0.183303 | intron-variant | Nck2 | GRCm38.p3 | 1:43482918 | GGAACCTCTGTGCCA[A/G]TGTGTCCCTTTGAGA | 17974 |
rs32226559 | snp | A/T | 0.46875 | 0.121031 | intron-variant | Nck2 | GRCm38.p3 | 1:43505561 | CTTTCTGGAGCCACG[A/T]GGACCGGAAAAGTTC | 17974 |
rs32228981 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | GRCm38.p3 | 1:43448643 | TCGAACTCAGAAATC[C/T]GCCTGCCTCTGCCTC | 17974 |
rs32257251 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Nck2 | GRCm38.p3 | 1:43461718 | CATGGCCTTTGCATA[A/C]GTTCCTGCTTCCAGT | 17974 |
rs32265262 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nck2 | GRCm38.p3 | 1:43467084 | TAGAAAGAGGAAGCC[C/T]GGAGTGTTTGATTGT | 17974 |
rs32318886 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Nck2 | GRCm38.p3 | 1:43499214 | CTTTTATGGTGGGTA[A/G]TGTCCCAGCATACCA | 17974 |
rs32324927 | snp | A/T | 0.375 | 0.216506 | intron-variant | Nck2 | GRCm38.p3 | 1:43466683 | CTAGTTTTAATGCCT[A/T]CAAGTTAGTATAATG | 17974 |
rs32325925 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nck2 | GRCm38.p3 | 1:43461803 | GAAGTGTAAGCCAAA[C/T]AAACCCTTTCCTCTC | 17974 |
rs32327588 | snp | C/T | 0.455 | 0.143091 | intron-variant | Nck2 | GRCm38.p3 | 1:43487376 | TGTGTGTCTTCTAAT[C/T]AGTTATGTAAATTGG | 17974 |
rs32328015 | snp | C/G/T | 0.444444 | 0.157135 | upstream-variant-2KB | Nck2 | GRCm38.p3 | 1:43444800 | AGTTCAGGAGCCTAC[C/G/T]GTCAATGGCTGCGAG | 17974 |
rs32368383 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nck2 | Mm_Celera | 1:43459240 | CCTTTGGCTTCAGAT[A/G]ACATGGATTAATGTA | 17974 |
rs32386149 | snp | C/G | 0.456747 | 0.140554 | intron-variant | Nck2 | GRCm38.p3 | 1:43455666 | CTCTTGTGTGGTCCT[C/G]TGTTCAACCACTGGG | 17974 |
rs32392731 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Nck2 | GRCm38.p3 | 1:43459115 | CTTTTCTAGAGGTGG[A/G]TAGGTGTCAGCCTTT | 17974 |
rs32429928 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Nck2 | GRCm38.p3 | 1:43461618 | TGGGGAGGGCAGAGC[C/G]TATGGTGGGGGATGC | 17974 |
rs32435062 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Nck2 | GRCm38.p3 | 1:43473252 | CTAAAATCATTACTA[C/T]GTAGGTTCGTTTAGA | 17974 |
rs32461997 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Nck2 | GRCm38.p3 | 1:43503115 | TCTCTGCGAAATTCT[C/T]GGAAATGTCGTGGTT | 17974 |
rs32470243 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Nck2 | GRCm38.p3 | 1:43452469 | GTGATACACAAAGAT[C/T]GTGTAAGGTTACAGA | 17974 |
rs32474719 | snp | A/G | 0.495 | 0.0497494 | intron-variant | Nck2 | GRCm38.p3 | 1:43456757 | TCAGTTGCGTGAGCA[A/G]TGGCTGATCAAAAGA | 17974 |
rs32502486 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nck2 | GRCm38.p3 | 1:43498346 | CTGAGCCGGGCTATG[A/G]GGACAACTGTTTTGA | 17974 |
rs32554465 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nck2 | GRCm38.p3 | 1:43460097 | CAGTATAGGGCCCTC[A/G]TCATATTTAACGATC | 17974 |
rs32562799 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nck2 | Mm_Celera | 1:43459242 | TTTGGCTTCAGATGA[C/T]ATGGATTAATGTAAA | 17974 |
rs32566544 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nck2 | GRCm38.p3 | 1:43502736 | ACCTGAGCATTCTAA[A/G]CTGAGATAAGCCTTT | 17974 |
rs32585472 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Nck2 | GRCm38.p3 | 1:43461090 | CTCTCCAGCCCAGAG[C/T]GGTTGTTTCTACAGT | 17974 |
rs32612853 | snp | G/T | 0.5 | 0 | intron-variant | Nck2 | GRCm38.p3 | 1:43485711 | CCAGCCCCCAGCTTA[G/T]AGCCTTGTCCATATA | 17974 |
rs32612870 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | GRCm38.p3 | 1:43463330 | CAGGCGAAGGCAGAT[C/T]CCTTTCCGCTTTCCT | 17974 |
rs32622882 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nck2 | GRCm38.p3 | 1:43499532 | CTGGAGGGGGTGCAG[A/G]TCCTGATCATTGTAC | 17974 |
rs32632670 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nck2 | GRCm38.p3 | 1:43499528 | TCTTCTGGAGGGGGT[A/G]CAGGTCCTGATCATT | 17974 |
rs32645438 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nck2 | GRCm38.p3 | 1:43466983 | GTTTTATTCCCTCTG[C/T]GCGCTTTGCCATTGC | 17974 |
rs32667316 | snp | G/T | 0.375 | 0.216506 | intron-variant | Nck2 | GRCm38.p3 | 1:43487016 | TCCCCTGATGTCACC[G/T]AGGGGGTTGGGTTGG | 17974 |
rs32687908 | snp | G/T | 0.49827 | 0.0293608 | intron-variant | Nck2 | GRCm38.p3 | 1:43511541 | AGCCCATGGGCGTAC[G/T]GAGCATGCCCATCAC | 17974 |
rs32707860 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nck2 | GRCm38.p3 | 1:43565551 | TTGTTTTATAGATCT[A/G]GGGATGAAAGGCAGC | 17974 |
rs32728253 | snp | C/G | 0.498615 | 0.0262793 | intron-variant | Nck2 | GRCm38.p3 | 1:43480193 | GCTGTGATGGAATGC[C/G]AGTTATCAAGTCTGT | 17974 |
rs32731273 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Nck2 | GRCm38.p3 | 1:43511319 | AGCACTTTACACTGA[C/T]GTCTTTATAATTTCC | 17974 |
rs32741226 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Nck2 | GRCm38.p3 | 1:43469247 | ACTAGGGATCTTTAA[A/G]CGTAGCATTGTGACT | 17974 |
rs32754109 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nck2 | GRCm38.p3 | 1:43461658 | GCTGGTGGTCTTGTG[C/T]TCTATAACCACAGAC | 17974 |
rs32761910 | snp | A/C | | | intron-variant | Nck2 | GRCm38.p3 | 1:43505451 | CCAGCACCCCCCCCC[A/C]AAAAAAAAAAAACAA | 17974 |
rs32763614 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Nck2 | GRCm38.p3 | 1:43474690 | AATGGCACAGCCCCC[A/G]GGTTTCTTTCTGTTT | 17974 |
rs32765609 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nck2 | GRCm38.p3 | 1:43506803 | TGGATTGCATAGTGA[A/G]CTCAAGGCCAACCTG | 17974 |
rs32785723 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nck2 | GRCm38.p3 | 1:43467459 | ACAGTGCTTCGCAAA[C/T]GGCCCCTGGACTGAA | 17974 |
rs32808530 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nck2 | GRCm38.p3 | 1:43463761 | GTTCTCCAAGGGGGG[A/G]AAAAATCTAAAAACA | 17974 |
rs32811639 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | GRCm38.p3 | 1:43448740 | AGTGTAATTTTTAAA[A/G]AGACTTTTAATTTTC | 17974 |
rs33412307 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Nck2 | Mm_Celera | 1:43456749 | ACCCTTTATCAGTTG[C/T]GTGAGCAATGGCTGA | 17974 |
rs33412311 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43456843 | TATTACCAAAGTTCA[C/T]GGGCTTGAGGGCTCA | 17974 |
rs33412313 | snp | A/G | 0.5 | 0 | intron-variant | Nck2 | GRCm38.p3 | 1:43457028 | TTGCTGACTCCCAGC[A/G]TCTACACAACTATGG | 17974 |
rs33413194 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43452754 | GTAAAAAGAGACTGT[C/T]AACTCCTCATGGAGT | 17974 |
rs33413197 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43452862 | AAAGGCTTGATTTGA[A/C]GCAGTTCACTGTGAG | 17974 |
rs33413199 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43452957 | ATGAGGACTCTCATA[A/G]ATACAGCGGAGAACA | 17974 |
rs33413201 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43452998 | TGCATGAGAAGAGAC[A/G]CCTTTGCTGACCCCT | 17974 |
rs33413766 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43457050 | CAACTATGGATTAGC[C/T]AGCCTAGGATATGAT | 17974 |
rs33413768 | snp | G/T | 0.486111 | 0.0821678 | intron-variant | Nck2 | GRCm38.p3 | 1:43457222 | ATTATTTCCTGTCCT[G/T]TCTTCTTCCTCTTTT | 17974 |
rs33413770 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43457279 | CGGTTCTGTTACTAG[A/G]ATGAATACTATACAA | 17974 |
rs33413773 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43457352 | TTATCTTTTCTCTAG[C/T]CCTATCTCCGATGGC | 17974 |
rs33414054 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Nck2 | Mm_Celera | 1:43453037 | TAAAAGTATAGGGCA[C/G]GGTCTGCTACCTCTG | 17974 |
rs33414057 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Nck2 | GRCm38.p3 | 1:43453075 | TGTGGTCTGCAAGCC[A/T]GTGAGTGCTCTTCCT | 17974 |
rs33414059 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43453367 | TATATCATCTTCTGG[C/G]CTTGCTCTCTGGCTA | 17974 |
rs33414060 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43453408 | CACCCATCTTCCAAT[C/T]CATCCTTGAAATTCC | 17974 |
rs33414063 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43453540 | AGAACAGCTTCTGAC[A/G]ACTCTTGCCATCTGT | 17974 |
rs33414405 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43459208 | CTTGGTTATTCCTGC[C/T]GAAGTAGCCTTCATT | 17974 |
rs33414408 | snp | A/C | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43459391 | GGATTAAAGGTAGAA[A/C]ATGTTGGATTCCTGG | 17974 |
rs33414411 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Nck2 | GRCm38.p3 | 1:43459457 | TTCTTGTTCAGTTTC[A/C]TTGAAAGTTGCAAGT | 17974 |
rs33414636 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43457530 | TGTTGTGAATCGGAT[G/T]TTTTGTAGATGAAGA | 17974 |
rs33414639 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Nck2 | GRCm38.p3 | 1:43457553 | GATGAAGAAATTATC[C/T]AAACTGGCCGTATGC | 17974 |
rs33414642 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Nck2 | GRCm38.p3 | 1:43457563 | TTATCCAAACTGGCC[A/G]TATGCTCCCAACTGT | 17974 |
rs33414985 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43453711 | CTTTGTTCTCCAAAA[C/T]CCACTCTCCCCTAAG | 17974 |
rs33414988 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43454159 | ATTACAAACATAATT[A/G]ATGTGTGACTAGACT | 17974 |
rs33414990 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43454199 | TTTATTTTTTTATTT[A/G]ATGAAGTCTTCAGAA | 17974 |
rs33414993 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43454375 | TATGTAGACATAGAA[A/G]CTAAAATCATGTTTT | 17974 |
rs33415034 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43459519 | ATTCAAGCATACACT[A/G]TTCTTTTGGATTTCA | 17974 |
rs33415037 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Nck2 | Mm_Celera | 1:43459554 | TGTAAAAACCTTGTT[C/T]TGTTTTATTACGCTG | 17974 |
rs33415040 | snp | A/T | 0.497041 | 0.0383476 | intron-variant | Nck2 | Mm_Celera | 1:43459777 | TTTTCTTGAGTATTG[A/T]GATTCACCAGTTTTA | 17974 |
rs33415043 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43459818 | GTTTGTTGCTGTTCA[A/G]AGGCCACCATGGTAT | 17974 |
rs33415285 | snp | A/G | 0.5 | 0 | intron-variant | Nck2 | GRCm38.p3 | 1:43457605 | TGGAGAGAGATCTGT[A/G]GTATGGGGATGTTTC | 17974 |
rs33415288 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Nck2 | Mm_Celera | 1:43457728 | TATTAAATTATATCA[C/T]TCTAAACTTGATTAA | 17974 |
rs33415291 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43457821 | TACTGATTTGGCTAG[C/T]TACACAATTGCATGT | 17974 |
rs33415293 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nck2 | GRCm38.p3 | 1:43457906 | TTACAGGGCTTTGGC[A/G]CTTTTATAGTTAGTG | 17974 |
rs33415526 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Nck2 | Mm_Celera | 1:43459897 | CTCCAATGATCTCCC[A/G]ATATAGCATAAGCTA | 17974 |
rs33415529 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43460048 | TAACTGAGACATAAC[C/T]AGCACCACTTTTTCT | 17974 |
rs33415532 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Nck2 | GRCm38.p3 | 1:43460061 | ACCAGCACCACTTTT[C/T]CTCACTTGGTTGTCT | 17974 |
rs33415889 | snp | G/T | 0.5 | 0 | intron-variant | Nck2 | GRCm38.p3 | 1:43454930 | TCTGACATGTGGGAA[G/T]GTCTTGAGGATTTCC | 17974 |
rs33415892 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43455026 | CAGCTGCTCAGACTC[C/T]CTTTGGGAACTATGG | 17974 |
rs33416116 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43457921 | GCTTTTATAGTTAGT[A/G]TGATGTAGTCCTTGA | 17974 |
rs33416119 | snp | A/C | 0.5 | 0 | intron-variant | Nck2 | GRCm38.p3 | 1:43458064 | TAGAGGTGACAGATC[A/C]TGTTATTCTTCAGAC | 17974 |
rs33416123 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43458182 | CAGGGCTGTGGGAGC[C/T]AGCCAGAGATCTACC | 17974 |
rs33416455 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Nck2 | Mm_Celera | 1:43460373 | TCTCTTCACATCACA[A/G]GTGCCGCTGCCCTAT | 17974 |
rs33416462 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Nck2 | Mm_Celera | 1:43461282 | GAAAAATACATTCTC[A/G]GGGCCTGCTTTGCAC | 17974 |
rs33416835 | snp | C/T | 0.5 | 0 | intron-variant | Nck2 | GRCm38.p3 | 1:43455050 | ACTATGGCACGGGAG[C/T]GTGTGCTCCAGACCT | 17974 |
rs33416840 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43455120 | CTTGGTAAGCCTTTT[G/T]CACGAGCATTGAAAG | 17974 |
rs33416842 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43455137 | ACGAGCATTGAAAGT[A/G]CCTGGAAATGATACA | 17974 |
rs33417225 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43464003 | TCTCACGCCTTAAGG[C/T]TTTTTGGCTCTCTGG | 17974 |
rs33417227 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43464182 | TTTAGCGATGCCTCA[A/G]AGGTGCGCTCTCAAA | 17974 |
rs33417229 | snp | A/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43464559 | CAGTTTGAGTGGACG[A/T]GCTCCCTTAGCTGTG | 17974 |
rs33417232 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nck2 | Mm_Celera | 1:43464754 | AGCTCCAAGTATTTT[A/G]TTGAGACCCAGATCC | 17974 |
rs33417307 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43458420 | CTGAGAGTTGTTCCC[A/T]GGTGTAGCTGTGTAC | 17974 |
rs33417310 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43458511 | AGTCAGACCATTTGT[A/T]TGCACACAGTAGACT | 17974 |
rs33417405 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43461295 | TCAGGGCCTGCTTTG[C/G]ACTTAATGACTTTTT | 17974 |
rs33417408 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43461405 | CTGCTATGGATTAGA[A/G]TCTGAGCCCTTCTCC | 17974 |
rs33417411 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43461421 | TCTGAGCCCTTCTCC[C/T]GACTTGGCTTGTGTG | 17974 |
rs33417724 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43455203 | TACCTCCGCTTCAGA[A/G]TGTATGAACTTTGGC | 17974 |
rs33417728 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43455963 | GGATTCTCTCTTCAC[A/G]ACTGTGTCTAATGGG | 17974 |
rs33417730 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43456029 | AACATCCCGCATATT[A/C]GTGCATGCATGGCTT | 17974 |
rs33417733 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Nck2 | Mm_Celera | 1:43456082 | TTGCTATCAGATTTG[C/G]ATTGGGAAATAGAGA | 17974 |
rs33417996 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Nck2 | Mm_Celera | 1:43452433 | ATACATAATCTTGAA[A/T]GTATGGGATGAAGAT | 17974 |
rs33418001 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43452690 | GGTCTGGGATCTGTT[G/T]ATTTTTCTCCGAGGA | 17974 |
rs33418035 | snp | A/C/T | 0.152778 | 0.230321 | intron-variant | Nck2 | Mm_Celera | 1:43470161 | TGGTACCTCCTCTTA[A/C/T]GGCGGACATTCTTAT | 17974 |
rs33418038 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | GRCm38.p3 | 1:43470192 | GAAGGGTCGCACCTG[C/T]ACCTGCCTTCTACTT | 17974 |
rs33418040 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43470231 | GGTGAAATACACAGC[A/G]TGGTTGTTTCTAGGT | 17974 |
rs33418042 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43470416 | ATAACTCAGAATTAG[A/T]CTGCCTGTGGTATCA | 17974 |
rs33418060 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43467331 | TATTTTTTTCATTTA[C/G]CCTTGTTTCCACAAT | 17974 |
rs33418063 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Nck2 | Mm_Celera | 1:43467400 | GTTCTAGCTTGGTGC[A/G]CTGATAAGACACATT | 17974 |
rs33418124 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Nck2 | Mm_Celera | 1:43462010 | AATGAATGACAGTTC[A/C]GAGACCTTCTATAGA | 17974 |
rs33418127 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43462108 | GTCTTCTGCATCTCC[A/G]AAATTACATAGGTTA | 17974 |
rs33418130 | snp | A/C/G | 0.42 | 0.183303 | intron-variant | Nck2 | GRCm38.p3 | 1:43462142 | AGCTTCATTGTATCC[A/C/G]TTTATGTGACTATAA | 17974 |
rs33418133 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Nck2 | Mm_Celera | 1:43462206 | AAATATAAATTCAAC[A/G]ATGTTTTTGAACTTG | 17974 |
rs33418295 | snp | G/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43464816 | TTACTTGCTTACTTA[G/T]AGATTTATTTATGAG | 17974 |
rs33418297 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Nck2 | GRCm38.p3 | 1:43465055 | CTAAAATGAGCAGAA[C/T]AGACTCCTTAAGACA | 17974 |
rs33418300 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43465143 | CAGCCTCTGTTTTTG[C/T]GGCCACTGTGTATAA | 17974 |
rs33418303 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43465223 | GACAACAGATGAAAC[A/G]CTCTTAGCCTTGGCA | 17974 |
rs33418580 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43459012 | GAATGTTTCTTTTTA[C/T]ATCAAGGTCCTGAAT | 17974 |
rs33418582 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43459040 | AATTTTTGTAAATGC[A/C]GCTTTTCAGACTGCC | 17974 |
rs33418606 | snp | A/C/G | 0.486111 | 0.0821678 | intron-variant | Nck2 | GRCm38.p3 | 1:43456162 | GAAAAACTTGATGGA[A/C/G]GCTTGAACATCCTTT | 17974 |
rs33418609 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43456407 | ATGCAATTTTCTCCA[C/G]ATAAGTGTTAGTGAA | 17974 |
rs33418612 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43456485 | TGAAAGTTATACGTG[C/T]TTAGAACGCCTGAAT | 17974 |
rs33418756 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43462688 | AGAGATGACAGATAT[G/T]AATTTCAGTGGCTTT | 17974 |
rs33418759 | snp | C/G | 0.459184 | 0.136902 | intron-variant | Nck2 | GRCm38.p3 | 1:43462832 | GTGAGCCAGGGGTTT[C/G]TGCTGATTCTTCAAA | 17974 |
rs33418762 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Nck2 | GRCm38.p3 | 1:43463143 | ACTTCACAGGGGTTT[G/T]TGGACTTGTGATCAA | 17974 |
rs33419056 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43465303 | ATATTTGGGGCACAG[A/G]GTAAATGGTAGAGTT | 17974 |
rs33419059 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43465367 | AAGAGAGGCCTGGGT[A/G]TTCCTTTGTTTAGTA | 17974 |
rs33419062 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43465457 | TGTGATTCATGTCAC[A/C]AACCTAAATGGTACA | 17974 |
rs33419108 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43467498 | GCTACCTTTTGTGTG[A/G]TCAGCCGTATTAGAA | 17974 |
rs33419154 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Nck2 | Mm_Celera | 1:43470612 | TTCCCAGTTTGCTCT[C/G]CACGGCGTCTCACTG | 17974 |
rs33419157 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43470618 | GTTTGCTCTCCACGG[C/G]GTCTCACTGATTGGC | 17974 |
rs33419159 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Nck2 | Mm_Celera | 1:43470860 | TTTAGCAGGTTGGTA[A/G]AAATATTTTTGGTCT | 17974 |
rs33419161 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43470934 | GTCTGGGCTTCACGC[A/G]CTGGCCTGGCATCTG | 17974 |
rs33419163 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43471395 | TCCCCTTCCCTCAGT[G/T]CAGGCTTGTAAGATG | 17974 |
rs33419325 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43456496 | CGTGTTTAGAACGCC[G/T]GAATACCACTTGTAC | 17974 |
rs33419327 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43456516 | ACCACTTGTACATCT[A/G]TGTCCTTAAATATGT | 17974 |
rs33419329 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43456609 | TCAGTCTGCTTATCC[A/G]TGTCCAGTCATCATA | 17974 |
rs33419434 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43482623 | AACACTTTGAGAAAT[C/T]CTCACACTCTGCCAA | 17974 |
rs33419437 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43482643 | CACTCTGCCAAGCCC[A/C]GTTTCCTTGTTAAGA | 17974 |
rs33419440 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43482652 | AAGCCCAGTTTCCTT[A/G]TTAAGAAAATTGGAT | 17974 |
rs33419443 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nck2 | Mm_Celera | 1:43482671 | AGAAAATTGGATGAG[C/T]ATCTCTCAGAAGGAA | 17974 |
rs33419444 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43473833 | CATGCTGCCTTCTAA[C/T]TAAGAGAATCAGCTA | 17974 |
rs33419447 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43473910 | CCTCTCAGCTGTTAT[C/G]ACAGGAGCACCACAC | 17974 |
rs33419450 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43474083 | AATGAACAGTGCAAG[A/G]CATAAAGTTGGCTAA | 17974 |
rs33419453 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43474104 | AGTTGGCTAAAGCTG[C/T]TTAGAGAGGTGCTGG | 17974 |
rs33419585 | snp | A/C/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43463162 | ACTTGTGATCAAAAC[A/C/G]GAAACCCAAACCAGG | 17974 |
rs33419588 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Nck2 | Mm_Celera | 1:43463228 | GTATTTCCTTTAAGC[A/G]TGACTTTAGTGGCAC | 17974 |
rs33419591 | snp | C/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43463300 | TCCATGTGGTTCCAC[C/G]GTGGCTGCATGCTGC | 17974 |
rs33419815 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43465485 | ACAGGAATACCAGAC[A/G]GCCATGTTACACACC | 17974 |
rs33419818 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43465574 | TGACAGCTGTACAAG[A/G]TTAAATTAAGCACAA | 17974 |
rs33419823 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43465931 | GCCTGAAACAGGCAG[A/G]TAGCCTACCAGAGGT | 17974 |
rs33419956 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43476460 | GAACATACTTAAACC[A/G]TATCCAAATCATAGC | 17974 |
rs33419959 | snp | A/C | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43476473 | CCATATCCAAATCAT[A/C]GCAAAGGCTGCTTCA | 17974 |
rs33419962 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | GRCm38.p3 | 1:43476505 | GTTAATTTCTTTGTG[A/G]AGGTTTTAACTGCCA | 17974 |
rs33420055 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43495058 | GATTATTGTATTCCA[A/G]GCTATTCAGAGTGAT | 17974 |
rs33420058 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43495084 | GTGATTTCTCTGTAT[G/T]TATGCTACCAGCTCA | 17974 |
rs33420061 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43495207 | TTTTCAGAGAAGTTT[C/T]GTGTGCTCTAACAGA | 17974 |
rs33420063 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43495312 | GCTGATGTGTATGCG[C/G]TTGGGCATATGGTGA | 17974 |
rs33420086 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43471519 | AGGCAGATGCTGTTA[A/G]GGATGGCAATGTGGT | 17974 |
rs33420089 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43471753 | ACACAGGACCCTATC[A/G]TCTGCCTGTGTTTAA | 17974 |
rs33420090 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43471794 | GCTGAGATAAAGGAT[C/T]GCATTTGTTGTGTTT | 17974 |
rs33420093 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Nck2 | Mm_Celera | 1:43471918 | AATGTCTCCTGTCTG[C/T]GTTCCCTCTCACTCA | 17974 |
rs33420186 | snp | G/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43467982 | TCCTGGCTTATACCC[G/T]ATGTCTTAATCTGTA | 17974 |
rs33420188 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43468027 | TTCATGGAAAATTTG[A/C]GGTAAATTTCAAAGT | 17974 |
rs33420191 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43468110 | ACCCGTGACCCCCGC[A/G]ACCACAACTGAAAAG | 17974 |
rs33420193 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43468201 | CCAACATATAGTCAG[C/T]GTGTCAATTTACTAC | 17974 |
rs33420216 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43474168 | TTGGGTGTGGCACTG[C/T]CCCTTAGATGCTCAC | 17974 |
rs33420219 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43474309 | TACATCTTCCTCCTT[C/T]TGCCCATTTCCACAA | 17974 |
rs33420220 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43474486 | TGTCTCCTGGTCCAC[C/T]CGAGGGCATTTTGAC | 17974 |
rs33420223 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43474500 | CCCGAGGGCATTTTG[A/G]CATGGCCAGAAAAAG | 17974 |
rs33420228 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43482755 | GGACTTGGGCATAGC[C/T]GCTAGGGGTTTTGTA | 17974 |
rs33420304 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43456639 | ACCTGTACCACATAC[C/T]TAGGAAGAGCCCATT | 17974 |
rs33420525 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43463372 | TTAGACCTGCCACTC[A/G]ATCTTGCTGGTCATT | 17974 |
rs33420530 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43463560 | GCCTGTAGAGAAAGG[A/G]CACACGGCATAGAAA | 17974 |
rs33420533 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43463578 | CACGGCATAGAAAGA[C/T]AGACCTGGCTGGAAC | 17974 |
rs33420786 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43466206 | ACTATTCTCGTTCTC[C/T]GTGAGGTTTTTATGG | 17974 |
rs33420789 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Nck2 | GRCm38.p3 | 1:43466355 | TGGGTGTGAAATGCC[A/G]CAGCACTCGCAGCTT | 17974 |
rs33420792 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Nck2 | GRCm38.p3 | 1:43466458 | GGAAGGAGTAGGAGA[A/G]CTTGGTCTGTTTTAA | 17974 |
rs33420884 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Nck2 | Mm_Celera | 1:43476513 | CTTTGTGGAGGTTTT[A/T]ACTGCCAGAATATTT | 17974 |
rs33420886 | snp | G/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43476528 | AACTGCCAGAATATT[G/T]TAACTTCACCCTTTT | 17974 |
rs33420887 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Nck2 | Mm_Celera | 1:43476712 | GTAATTCCCTAGTAG[A/G]GATTTTGCTTTGTGG | 17974 |
rs33420889 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43476746 | CCTCTGTTCAGATTG[C/T]GGCATTCATTTCTTT | 17974 |
rs33420891 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43476905 | TGAACAGACCCACTG[A/G]GCCTCAATGGCTTGT | 17974 |
rs33420893 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43476921 | GCCTCAATGGCTTGT[A/G]TTTCTTCAATTCTTT | 17974 |
rs33421016 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43495351 | TGCTTTCTTGTGATT[C/T]TCTAGGTGTTGTATT | 17974 |
rs33421019 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43495371 | GGTGTTGTATTTTAA[C/T]AACTGTTTCCACAGC | 17974 |
rs33421022 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43495849 | TATACTTTGCCCAAG[C/T]GAGGGTCGCAAGACA | 17974 |
rs33421076 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43471993 | TGCATGTCACTCTTG[A/G]CTTAGCATACAGTCA | 17974 |
rs33421079 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Nck2 | Mm_Celera | 1:43472274 | GCCCTCTCACCTAAG[C/T]GAGGAGTTCCTGTTT | 17974 |
rs33421082 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43472406 | GAAGTGCTCCAGTGG[C/T]TTGGTGGCTGACACA | 17974 |
rs33421166 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Nck2 | Mm_Celera | 1:43468308 | CAGCTGGAATAGCCA[C/T]ATCCTGAGGAAGCAA | 17974 |
rs33421171 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43468710 | TGTGTGTGGCTGGGG[C/T]AGTGAGTGGCTCCAG | 17974 |
rs33421278 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43474565 | GTGGAGCAGGCTGCC[C/T]TTCTTCTTCCAGCTG | 17974 |
rs33421315 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43482903 | GGAAGCAGAGCTGGC[A/G]GAACCTCTGTGCCAA | 17974 |
rs33421319 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43482950 | GTCACAGTGTCACAG[C/T]CGCTGCCGCTGGAGG | 17974 |
rs33421635 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43466489 | CCTGCCATAGATACC[G/T]TGCTCTCTGAGGGCT | 17974 |
rs33421638 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43466532 | CAGAGCCCATCTACA[C/T]TGTGGCCTGTGCTAG | 17974 |
rs33421641 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43466645 | TCTGTTGCCTTCTGT[A/G]ATGAGGTCTGTTAGA | 17974 |
rs33421805 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43495960 | GAAGGGATAATTACA[G/T]CGACGTCTGTCTAAA | 17974 |
rs33421808 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43495996 | TAATCATATGCCAAG[A/G]TAGTTAGAAACTACA | 17974 |
rs33421810 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43496172 | TTGCTGTTAAGTACC[C/T]TGTAATGCTGGGACA | 17974 |
rs33421813 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43496259 | CCTGTCAAGTTCAAC[C/T]AGGCATTTGCGGGCT | 17974 |
rs33422014 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Nck2 | Mm_Celera | 1:43468754 | TTTCCAGTTTCCTTC[A/C]GAAAATCACCCCAAG | 17974 |
rs33422022 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43469429 | GTCTCATAACCGTAG[C/T]GCTCTGGATCTGCTC | 17974 |
rs33422126 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43477007 | TACCTTTTATATGGT[A/G]TTATTTTAACTAAGC | 17974 |
rs33422129 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43477273 | ATACACCTTTTCTTT[A/C]AATTAGTACGTGTTA | 17974 |
rs33422132 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Nck2 | GRCm38.p3 | 1:43477484 | CAGAATGGTGAGTTT[A/T]ATGTGACATACATGC | 17974 |
rs33422325 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43474753 | TTTCCCAGATGACCT[C/T]TGCCTCACTCCCCTG | 17974 |
rs33422330 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43475008 | CTGCACAGGAACCTG[C/T]TGTTCTTGGCCATGA | 17974 |
rs33422332 | snp | C/G/T | 0.132653 | 0.220748 | intron-variant | Nck2 | GRCm38.p3 | 1:43475071 | CCTGTGTCTCTTCTA[C/G/T]GATCACAGCAGGGCC | 17974 |
rs33422399 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43472875 | TGGACAGTGTAGTTA[A/G]ATCTGACACAATTGC | 17974 |
rs33422465 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43484249 | TCTTCCCACCTTTCT[A/T]GTATTTCTCTGATAA | 17974 |
rs33422468 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43484644 | ACTTGGAAAAAGGCA[A/G]AGTTGGATAATGATC | 17974 |
rs33422471 | snp | A/C | 0.426035 | 0.177515 | intron-variant | Nck2 | Mm_Celera | 1:43484785 | AGCCAAGGAAAAAAA[A/C]ATCACATTTATATGC | 17974 |
rs33422526 | snp | G/T | 0.489796 | 0.070696 | intron-variant | Nck2 | Mm_Celera | 1:43466725 | CCTTTGTTTTCAGGG[G/T]TTTTTTGTTTCTGTT | 17974 |
rs33422529 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Nck2 | Mm_Celera | 1:43466797 | GTGTTGGTCTCAGAA[C/G]CCTGCTGTCCTTTAA | 17974 |
rs33422533 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43466822 | CTTTAACTCCTTCCA[G/T]GTGGGTTGCACATAG | 17974 |
rs33422706 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43496337 | ACTTTGCTGCTCCTT[C/T]AGCAAAACCAGACGT | 17974 |
rs33422709 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43496365 | CGTTTACAGCTAGGA[C/T]GGTATGAAGACACCA | 17974 |
rs33422712 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43496499 | AATTTCGGTTGGTCA[C/T]TGGCCTCACAAAAAC | 17974 |
rs33422765 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43480274 | CTGCTCTGAGGCAGG[C/T]AAACCTGAAGGAGAT | 17974 |
rs33422769 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Nck2 | Mm_Celera | 1:43480426 | AAATAAAAAATACCT[C/T]AGCTAAACGGTTAGT | 17974 |
rs33422772 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43480442 | AGCTAAACGGTTAGT[C/T]TTGTCTGGATTACGT | 17974 |
rs33422935 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Nck2 | GRCm38.p3 | 1:43477526 | GGAGTTTGGGTTTAA[G/T]TTCTGATGTTTATCC | 17974 |
rs33422938 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43477558 | CATTTTTCATGGCCT[A/C]TGTCATGTTGATATG | 17974 |
rs33422941 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Nck2 | GRCm38.p3 | 1:43477947 | CTGTCTGGTGGCAGC[C/T]CTGATGGACAGAGAA | 17974 |
rs33423085 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43469444 | CGCTCTGGATCTGCT[C/G]GGCCTCATCTAGCCA | 17974 |
rs33423088 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Nck2 | Mm_Celera | 1:43469529 | AGGGTTTTGAGTTCT[C/T]AGTGATGTCTTTAGC | 17974 |
rs33423091 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43469574 | TGTGGTGCTTCTGCA[A/C]GGCGTTGTTTTACCC | 17974 |
rs33423394 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43475175 | CCATATGGAGAATTG[C/T]CTGTGAGGTCCTGAT | 17974 |
rs33423396 | snp | G/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43475221 | GCACTCAGATTCTTT[G/T]AAGTGTGGGTGGAGA | 17974 |
rs33423398 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43475235 | TGAAGTGTGGGTGGA[A/G]ACCTAATGTTCGACA | 17974 |
rs33423400 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43475253 | CTAATGTTCGACATC[C/T]GGTTGGAGTGGATAG | 17974 |
rs33423403 | snp | A/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43475285 | TTGCCTGTCATTGTA[A/T]GGGTCAGTGTAATTG | 17974 |
rs33423446 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nck2 | Mm_Celera | 1:43485179 | AATTCTTAAACTGGG[C/T]TATCCTTATCCTTCC | 17974 |
rs33423449 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43485271 | TGTCCGCTCATGCCT[A/G]TTTACCTAGTCTTCA | 17974 |
rs33423452 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43485322 | CCTCTTTGAATGTCC[A/G]TCCCCTCTAGTGCAT | 17974 |
rs33423585 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43466861 | AGGTCGCTGTGTGAG[A/G]TGGATGGTGCTCAGC | 17974 |
rs33423587 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43466883 | GTGCTCAGCAGCACA[C/T]GGAACCAGGGGCTGC | 17974 |
rs33423605 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43496530 | AGGCAAAGTTAGGTG[C/T]GTGCATCAGTTGAGG | 17974 |
rs33423608 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43496568 | CACTGTCTCATACAT[C/T]GGCAGCATTGGCGGT | 17974 |
rs33423611 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43496637 | GGAGTTCATTCAGCG[C/T]CACATATAAGTGCCT | 17974 |
rs33423666 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43488637 | CTTGGCCATCAGCCG[C/T]TGTAATTCAGTGCTC | 17974 |
rs33423669 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43488670 | TCCTTTAAATTGAAA[A/G]CCATCTGTACTAATT | 17974 |
rs33423672 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43488902 | AGTGAGAGGCCGGGC[A/G]CCTCGTAAGCATTCA | 17974 |
rs33423734 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43477973 | GAGAAGGCAGTGGTG[G/T]GCCCCTGATCATCAG | 17974 |
rs33423737 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Nck2 | GRCm38.p3 | 1:43478032 | GTTGTAGTTTTGGAC[A/C]CGATGATGGAAATTG | 17974 |
rs33423740 | snp | A/C | 0.32 | 0.24 | intron-variant | Nck2 | GRCm38.p3 | 1:43478068 | TTGGGACTTGCCAGA[A/C]AAGTTAGAGAGTTAC | 17974 |
rs33423743 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Nck2 | Mm_Celera | 1:43478079 | CAGAAAAGTTAGAGA[G/T]TTACAGAAAATGGCA | 17974 |
rs33423745 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43480601 | TAGCAAGCAATGGGA[A/G]TACATGTTCTTGTCC | 17974 |
rs33423748 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Nck2 | GRCm38.p3 | 1:43480883 | GAGGCTTATGTTTTA[A/G]TTATAAAAGTCACAT | 17974 |
rs33423751 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43480975 | TTCACACTGGTCCTA[A/G]CTTCTTCTGCTTGTG | 17974 |
rs33423828 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43473412 | ATGTGGCTTCTTCCT[C/T]GATGAGAACTTGACT | 17974 |
rs33423831 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43473426 | TCGATGAGAACTTGA[C/G]TCTTTTGTATGCGTT | 17974 |
rs33423833 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43473756 | TTCTTTTTTCTTGTC[A/G]TCTTTTCAGTTGTTT | 17974 |
rs33423914 | snp | A/T | 0.473373 | 0.11227 | intron-variant | Nck2 | Mm_Celera | 1:43469697 | TTTTTAGGTTTTTTT[A/T]ATATGAAGCTGCATT | 17974 |
rs33423917 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43469711 | TAATATGAAGCTGCA[C/T]TCAGGACTAGGAGCC | 17974 |
rs33423920 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43469750 | GTCTCAGATCTTGCC[C/T]TCTTCAGTCAGCCTG | 17974 |
rs33423922 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43469771 | AGTCAGCCTGTATCA[C/T]GTAGATTGTTTCTTG | 17974 |
rs33424094 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Nck2 | Mm_Celera | 1:43498683 | TTTGTACACCAAAGG[A/T]TTTTTTATAAATGAA | 17974 |
rs33424097 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nck2 | Mm_Celera | 1:43498870 | CACTATGCCCTGCTC[C/T]TTTTTTCAAATGACA | 17974 |
rs33424100 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43499107 | AATGAATCTGGATGA[A/G]AATAAGATGGCAACA | 17974 |
rs33424125 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43485461 | CCAGGGCAGGAATTA[C/T]GGCAAATGTTACGAA | 17974 |
rs33424127 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Nck2 | Mm_Celera | 1:43485536 | CTGAGCACTAGCTGT[A/T]TGTGAGTGGTCATCT | 17974 |
rs33424132 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Nck2 | GRCm38.p3 | 1:43485879 | CCCCTCTTGTGTGGG[A/T]CTGGAGTTCTGTTTC | 17974 |
rs33424214 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43496696 | GCCCTGGGTTGAGGT[A/C]TACATTCCCTTTCTC | 17974 |
rs33424217 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43496756 | CTCTCATAAAACACA[A/G]CCAAGCCATGACCAC | 17974 |
rs33424220 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43496951 | AGTTTAATCATGTAT[A/T]TAAGCATGGATGGAA | 17974 |
rs33424223 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43497220 | CAAGGCAAGCAGATC[C/T]CATCTGGCCAGCATT | 17974 |
rs33424386 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43503695 | TGAGGTGTCTCCAGT[G/T]GGCTTTTGTTCGTTT | 17974 |
rs33424389 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43503830 | TGGAGCAACATCCTT[C/T]TCATTGGCTTGTTGC | 17974 |
rs33424392 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43503921 | ACCTGTGGATATTCT[A/G]CTTTGCCAGTTCTAA | 17974 |
rs33424406 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Nck2 | GRCm38.p3 | 1:43478158 | CTGCCTAAACTGCTG[A/G]CTAAGCAAAATGGTC | 17974 |
rs33424409 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Nck2 | GRCm38.p3 | 1:43478293 | GTCACTGTACCTGCT[A/G]TGGTCTGCCTTCCAG | 17974 |
rs33424412 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43478345 | TGTCCCTGGAGCAGT[G/T]AGTTAGTGAGGTCCA | 17974 |
rs33424454 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43481061 | CCCTCTCTCTGAAGG[A/C]ATTTCTTGGTCTTTA | 17974 |
rs33424457 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nck2 | GRCm38.p3 | 1:43481113 | GGTGTGCCATGCACC[C/T]TCAACTTCTCCATCT | 17974 |
rs33424460 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43481136 | CTCCATCTTTGTGTG[A/G]CCCCCATCTGCTATG | 17974 |
rs33424463 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Nck2 | GRCm38.p3 | 1:43481137 | TCCATCTTTGTGTGA[C/T]CCCCATCTGCTATGC | 17974 |
rs33424525 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43489117 | GGACCCACCTTGCAA[A/T]TTGGGATTCTCAAAG | 17974 |
rs33424528 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43489647 | TAATAAAATTCTACA[A/G]TGAGCCCTGAGTCAA | 17974 |
rs33424531 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43489810 | TGTAGAATGCTGTTT[C/T]CTATTTGTAGGACTG | 17974 |
rs33424546 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43475356 | GTCAAAGCTGAAAAC[A/G]TGGTTCTTGACAGGC | 17974 |
rs33424549 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43475404 | CTAGGGTTGAAGGGG[C/T]TTTCAGAAACCTGGT | 17974 |
rs33424553 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43475627 | GCAGTCTCCTGACTG[C/T]TTCCTGGCACACACC | 17974 |
rs33424584 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43466985 | TTTATTCCCTCTGTG[C/T]GCTTTGCCATTGCAG | 17974 |
rs33424589 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43467113 | GTGGAGTCCTGTCTG[C/T]TCCTTTCATTAGATC | 17974 |
rs33424725 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43469839 | AGTTACAATATGGGT[A/C]AGGTTGGGTAGAACA | 17974 |
rs33424728 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43469930 | GCAAGACAAGCAGAG[C/T]GGTGCCTTGTGCCGA | 17974 |
rs33424731 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43470002 | ATAACCGCTATGGAA[C/T]TAAGCGGATCCTGGC | 17974 |
rs33424733 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43470063 | TTTCCTACTCTGAGC[A/G]TGTCTTTGTACAGAT | 17974 |
rs33424966 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43497306 | AATAGAGAACCTGAC[A/G]TTCAGGAGCATCTCA | 17974 |
rs33424969 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43497412 | CTCCTGTTGCTGGCT[C/T]TGTGTACCTGTCTGT | 17974 |
rs33424971 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Nck2 | Mm_Celera | 1:43497592 | CTTTTAAATCTCCGC[A/T]TCTCTGGCTTGTCTC | 17974 |
rs33424973 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Nck2 | Mm_Celera | 1:43497622 | CACAAGAAGGAAAGA[A/T]CTTTCTAGACTGTTC | 17974 |
rs33424985 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43499284 | CCAATCTATCTCAGC[C/T]TGTGACTGCCCCTGG | 17974 |
rs33424988 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43499489 | TCCTGCGTTGTCAAA[A/T]ATCAGCACTTCCCCT | 17974 |
rs33424991 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nck2 | GRCm38.p3 | 1:43499492 | TGCGTTGTCAAATAT[C/T]AGCACTTCCCCTAAC | 17974 |
rs33425015 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43485927 | ATGTTGCTCCTCTCT[A/C]GGATGGCTTGGCCTC | 17974 |
rs33425018 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43486069 | TGAGCACATCTTGCA[C/T]CTCTGTCATCTGTGG | 17974 |
rs33425021 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43486944 | TAGTAACTTTACCCA[C/T]AATGGTGTTCCTGTG | 17974 |
rs33425023 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Nck2 | Mm_Celera | 1:43487063 | TCACTTTTTATTTTA[A/G]TTCTGATCTGTGTTT | 17974 |
rs33425085 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Nck2 | GRCm38.p3 | 1:43478440 | TGACATCTCCCACAG[A/T]CCTGAGTTAGCAGTT | 17974 |
rs33425088 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Nck2 | GRCm38.p3 | 1:43478602 | GTCTTACTTAACCTT[A/G]ACTCAGGAGGATAAA | 17974 |
rs33425091 | snp | A/C | 0.497041 | 0.0383476 | intron-variant | Nck2 | GRCm38.p3 | 1:43478613 | CCTTGACTCAGGAGG[A/C]TAAAAATTTGAAGTT | 17974 |
rs33425125 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43503972 | GGTCATTTAATTCAT[C/T]ATTGGAACCTTTCCC | 17974 |
rs33425128 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43503989 | TTGGAACCTTTCCCA[A/G]ATCTCTGTCTGCCTC | 17974 |
rs33425131 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43504062 | GTTTTGGCTTTGCTC[A/G]AACATTTTCTTGTGA | 17974 |
rs33425236 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43481219 | TTAGCTTCTCTTTGC[A/T]TTGCCTTCCCCCTCT | 17974 |
rs33425239 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Nck2 | GRCm38.p3 | 1:43481250 | TTCCAGGCCTTCAGT[G/T]TTCTTTGGTGGCCAG | 17974 |
rs33425242 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Nck2 | GRCm38.p3 | 1:43481269 | TTTGGTGGCCAGGCA[C/T]ACTGGTCTGGCATGA | 17974 |
rs33425266 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43473797 | CTTAAACAGATTCTA[C/T]TATCAACAAGATAGC | 17974 |
rs33425436 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43491655 | TCTCTGCCTATCCTT[A/C]GGTCATCTTGCATGA | 17974 |
rs33425439 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nck2 | GRCm38.p3 | 1:43491782 | ACTGTGAACCTACTT[C/T]GCTCCGTGCACCTGA | 17974 |
rs33425442 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43492602 | ATGCTTATTTTTACT[A/T]ACTTGAAAGAAGGCC | 17974 |
rs33425505 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43475652 | CACACCTGCCCTGAT[A/T]ATTGCCAGGAACCAA | 17974 |
rs33425507 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43475676 | GAACCAAGGGAAGGG[C/T]CAAAGCAATGGTCGG | 17974 |
rs33425510 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43475811 | GGTCACCCTTATGGT[G/T]CCTCTGTGTGCCTCC | 17974 |
rs33425513 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nck2 | Mm_Celera | 1:43475900 | TAAAAAGCCCAAGAG[C/T]TTCAAGAGTTTGTTC | 17974 |
rs33425526 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43470149 | AGGAAACACACTTGG[G/T]ACCTCCTCTTATGGC | 17974 |
rs33425605 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43507838 | GTTGCATGTGTTTAA[A/G]CATGGTTGTGATATG | 17974 |
rs33425608 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nck2 | Mm_Celera | 1:43508094 | TCTTTACTTTCTATT[C/T]CATGTGAGGTTAGCA | 17974 |
rs33425611 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43508343 | AGATTGCTAGATCCA[A/G]CAGCTGCACAAGTAT | 17974 |
rs33425834 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43499594 | TATCTCTTTTCATTC[A/G]TGTATTCTTTGAAAG | 17974 |
rs33425837 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Nck2 | Mm_Celera | 1:43499707 | CACCAAGTCTTACTG[C/T]TATCTCAGTTTTGGG | 17974 |
rs33425840 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43500158 | GCAGGAGGAGTAAGT[A/G]TGGTGGCCCTCTGTG | 17974 |
rs33425843 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43500190 | AATCTGTCCCCTTTC[A/G]TCTCCGGGTTTACAC | 17974 |
rs33425854 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Nck2 | GRCm38.p3 | 1:43478625 | AGGATAAAAATTTGA[A/G]GTTGGTTGGCTAGTC | 17974 |
rs33425856 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43478737 | TTGGGAGGAGCCAGG[C/T]TTACTGAAAACAACT | 17974 |
rs33425858 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | GRCm38.p3 | 1:43478770 | GTGTCACAGAGCTGA[C/T]CTCAGACTTGATGAG | 17974 |
rs33425861 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43478967 | TAGCTGCTTTGAAAC[C/T]AGGATCAAACGGTGA | 17974 |
rs33425900 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43487577 | TCACAGTTGAAATGA[C/T]GGCTTTCAGCCTTTC | 17974 |
rs33425902 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43488398 | AATCCCCTTTGACAA[G/T]TAGTGTAAGAATAGA | 17974 |
rs33425934 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43504191 | ACATTGCTGTGTGGA[A/G]TTGAAGTTGATCATT | 17974 |
rs33425937 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Nck2 | Mm_Celera | 1:43504262 | TATCTGAGACCTGCT[C/T]GGACAAGGATGGGGT | 17974 |
rs33425940 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Nck2 | Mm_Celera | 1:43505066 | AACCTGATAGGTAAA[G/T]ACAGTTTGTAAGTAT | 17974 |
rs33425943 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43505093 | GTATAACTCTCCTTA[G/T]GTTGTGCTTTTGTGT | 17974 |
rs33425985 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43497817 | GGATGGGCCCACCAG[C/T]CCATTGTGATAGTGG | 17974 |
rs33425988 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43498004 | GTGGAAGCTAGAAGT[C/G]CTTGGATTTGTGAGA | 17974 |
rs33425989 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43498133 | TAGATGAGACAAAGT[A/G]TCCACATGTCGGCCT | 17974 |
rs33425992 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43498209 | AAGAAGAAACCGCTT[A/G]TGAATCTGCTACTCA | 17974 |
rs33426085 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Nck2 | GRCm38.p3 | 1:43481289 | GTCTGGCATGAGACA[C/T]ATGCAGTTTGTCTGG | 17974 |
rs33426087 | snp | A/G | 0.18 | 0.24 | intron-variant | Nck2 | GRCm38.p3 | 1:43481355 | TTATTATACATGAAG[A/G]GCATCAGTGTGTCTG | 17974 |
rs33426090 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Nck2 | Mm_Celera | 1:43481617 | ATCAGCCTTGTCAAC[C/T]CCTCAGTTTCTTGGA | 17974 |
rs33426093 | snp | A/C | 0.426035 | 0.177515 | intron-variant | Nck2 | GRCm38.p3 | 1:43481618 | TCAGCCTTGTCAACC[A/C]CTCAGTTTCTTGGAG | 17974 |
rs33426205 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43492782 | CTGTCCTTAATATTT[C/T]TTTATTCCTGCACAC | 17974 |
rs33426209 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43493207 | CCAGCTAAGGTACAG[C/T]GTGCTGACTTTGCAC | 17974 |
rs33426212 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43493299 | GAAGCTCTAGGTTCC[G/T]GGTTTGGCCTCACCG | 17974 |
rs33426386 | snp | A/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43476004 | TACTAAGAATTGATA[A/T]TAAATGTATCTGTTA | 17974 |
rs33426389 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43476036 | AATATCTTCTGGAGA[A/T]AAAGGGGATCCAAAA | 17974 |
rs33426392 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43476073 | TGTGTTAATTTAAGG[A/T]TGTCTTGATCTGTTT | 17974 |
rs33426474 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43508467 | ATATAGAGGTGGTCG[A/G]TAGGGCCATGGCCAA | 17974 |
rs33426477 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43508543 | ACCAGCTCTTCATTT[C/T]ATCTTATAGTAAACA | 17974 |
rs33426480 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43508550 | CTTCATTTCATCTTA[C/T]AGTAAACACCTACAG | 17974 |
rs33426483 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43508643 | ACTGTTAAAACCATC[C/T]GACTCTTGAGATAGA | 17974 |
rs33426566 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43500196 | TCCCCTTTCGTCTCC[A/G]GGTTTACACTGGGGC | 17974 |
rs33426569 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43500230 | GAACACAGTTAAAGG[G/T]AACACACTCTGAAGG | 17974 |
rs33426572 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43500347 | TGGAATGAGGTGTCA[C/T]ATGGCTGTTAGGAGT | 17974 |
rs33426704 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43511463 | GTTGTTATCCCATCA[C/T]CGCCCACAGAGAGCG | 17974 |
rs33426707 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43511616 | AGAAATGGACATTGA[A/C]GTGGAGCCCTATTAG | 17974 |
rs33426708 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43511652 | AGTAATTTGCGAATG[C/T]TCACCTATCAATCCG | 17974 |
rs33426710 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43511669 | CACCTATCAATCCGT[C/T]TGTCAAATTTCATGG | 17974 |
rs33426713 | snp | A/G/T | 0.244898 | 0.249948 | intron-variant | Nck2 | GRCm38.p3 | 1:43511754 | AATTCACCAGGAATA[A/G/T]ACCGGCACTGATTAT | 17974 |
rs33426718 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43505403 | CCTGTCTCCAAAGCA[A/G]ACACAAGCAGAACAG | 17974 |
rs33426723 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43505659 | GGGAATAGAAGGTGA[C/T]CTTCCAGAAGAGCCT | 17974 |
rs33426734 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Nck2 | GRCm38.p3 | 1:43479008 | CAGCCATATGCTAGG[C/T]GCTTCTGACTGAGGA | 17974 |
rs33426737 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43480189 | TCTGGCTGTGATGGA[A/G]TGCGAGTTATCAAGT | 17974 |
rs33426741 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43480226 | GTGCCCATGATGGTT[G/T]TCCTGTTGGTTGCTA | 17974 |
rs33426915 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43488460 | GGGTGCGGTGATGAC[A/G]TGGAACTATGTGTTA | 17974 |
rs33426918 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43488590 | TATTTATCCACTTCT[A/T]GTTTCACTCCTGTTC | 17974 |
rs33426975 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43498227 | AATCTGCTACTCAGA[A/G]ATTTGGTGGTTTGGT | 17974 |
rs33426978 | snp | A/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43498322 | TGCAGGTTTAAGCAG[A/T]GTAACCATCTGAGCC | 17974 |
rs33426981 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43498416 | CTCATTTACAGGCGC[C/T]CTGTCTTTTTCAGAG | 17974 |
rs33427045 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Nck2 | GRCm38.p3 | 1:43481682 | TCTCTCTAGGGGGCT[C/T]TAAAGGTCACAGTGG | 17974 |
rs33427048 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Nck2 | GRCm38.p3 | 1:43481714 | ATGCTTACCTCACTG[C/T]TTTTTGTGCCTGATT | 17974 |
rs33427050 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | GRCm38.p3 | 1:43481742 | ATTCCCTGTAGCAGT[A/G]ACATACAGTGACCCT | 17974 |
rs33427053 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43481832 | GTTTGAATAATAAAG[G/T]GTCTGGCGAGGGGAA | 17974 |
rs33427085 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43493305 | CTAGGTTCCTGGTTT[A/G]GCCTCACCGTCAGCT | 17974 |
rs33427088 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43493424 | CATTTTTTTTTAAGC[C/T]CTTTAGGCTGTCACA | 17974 |
rs33427091 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43493689 | AGCTGTCCTCAGAGA[C/T]GTGTGCATAGTTCAA | 17974 |
rs33427195 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43476245 | CTTCTTAATGAGTTT[A/G]GAAAGTAATCAAGAT | 17974 |
rs33427198 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nck2 | GRCm38.p3 | 1:43476445 | ACCGGAGCCCTTGGG[A/G]AACATACTTAAACCA | 17974 |
rs33427356 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43508850 | CCTCCAAGTGAGCTG[C/T]CAGGACAGATGCCCT | 17974 |
rs33427359 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43508966 | AACCAGAAGTGTTTG[C/T]CCAAGTGTGTGCACA | 17974 |
rs33427362 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43508994 | ACAGTGACTGCACTG[C/T]CAATTCCACAAGCAG | 17974 |
rs33427474 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43500391 | TATGTCCATGACACC[A/C]TGGGCATGTTTCTCC | 17974 |
rs33427477 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43501191 | GAGTTATGTATGAGA[A/G]ACCCTGAGAGACCCC | 17974 |
rs33427480 | snp | A/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43501325 | TGAAGTGGTAGAGCC[A/T]TTTAGAATAGAACCT | 17974 |
rs33427483 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43501472 | TGGGGTGAGCAGCCT[G/T]GTTTCACTTCTGTTC | 17974 |
rs33427614 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Nck2 | Mm_Celera | 1:43526804 | AAAACCTGCATCATA[C/T]GGCCTGTGCATTTTA | 17974 |
rs33427616 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43526808 | CCTGCATCATACGGC[C/T]TGTGCATTTTATGTT | 17974 |
rs33427618 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43526849 | CTAAATTACAGGCAT[C/T]GTGAATAATAAGGCA | 17974 |
rs33427620 | snp | C/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43526943 | TGATTGAAATTGCAG[C/G]TTCTTTTATGGTTGC | 17974 |
rs33427622 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Nck2 | Mm_Celera | 1:43527027 | TTATTTGTCTTGGGT[A/C]ACTTTGGAAACACAT | 17974 |
rs33427666 | snp | A/G | 0.5 | 0 | intron-variant | Nck2 | GRCm38.p3 | 1:43505678 | CCAGAAGAGCCTCTT[A/G]GAATTTGTGTCTCAA | 17974 |
rs33427669 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | GRCm38.p3 | 1:43505733 | AGGCAGAGATGTTTC[C/T]GAGAGAGAGAAAACA | 17974 |
rs33427672 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43505831 | ATTTTAAAACAGCTA[A/C]ATATAAGCACAATAT | 17974 |
rs33427734 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43498464 | GCCTCCAGGAGAACT[A/G]TGAGCACAGATGTCC | 17974 |
rs33427865 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43531525 | TATGCTTTCAGCATG[A/C]ACTGAAATAAACGCA | 17974 |
rs33427867 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Nck2 | Mm_Celera | 1:43531711 | TCCCCTCTGAACCTC[A/T]TTTTTATTACTATTG | 17974 |
rs33427869 | snp | C/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43531911 | AACTCTACCCTCTTG[C/G]ATATTATGTGCATTA | 17974 |
rs33427872 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43532185 | CTGAAGGGTGTGTCC[A/C]GTCAGTAGAGGGGCT | 17974 |
rs33427874 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43493735 | CCATTGATTTCAATT[A/G]AATGTCCCATTGATT | 17974 |
rs33427877 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43493836 | GCTGGCATTTGCTGA[C/T]TAGATCTTCCTAGAG | 17974 |
rs33427880 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43494011 | ATATAAGTGGTCCCT[A/G]TAGATAGCCTGGGTG | 17974 |
rs33427883 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43494062 | TAATGTGTTCCTTCC[A/G]TATTTGCTACTCAGA | 17974 |
rs33427926 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nck2 | GRCm38.p3 | 1:43481833 | TTTGAATAATAAAGT[A/G]TCTGGCGAGGGGAAC | 17974 |
rs33427928 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43481928 | CCTAGGTCCTGCTGG[A/G]CTTGGGACTTCTAGG | 17974 |
rs33427931 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43482040 | GGAGAGAGCAGGTCT[G/T]GCAGCCCCTGGCTAA | 17974 |
rs33428006 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43511770 | ACCGGCACTGATTAT[A/G]AAGAAGTTGATAATG | 17974 |
rs33428008 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Nck2 | GRCm38.p3 | 1:43511847 | AGGGAGAGCGCTATG[C/G]TGGCTCCTGGCTCTC | 17974 |
rs33428011 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Nck2 | GRCm38.p3 | 1:43511887 | GGACCAGCCTGCATA[C/G]TCAGCAGGGTGCGTT | 17974 |
rs33428216 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Nck2 | Mm_Celera | 1:43501901 | ACTATGACAAGTTAT[A/G]TATCATGCAGAAGCA | 17974 |
rs33428219 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43502069 | GGAGTTTTGTTGGCT[A/G]TGGGTAGGAGTGATC | 17974 |
rs33428222 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43502206 | TGGGGGCAGGGTGGC[A/G]TCCCTGTGGTGTTGT | 17974 |
rs33428234 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Nck2 | GRCm38.p3 | 1:43509070 | TTGTAGCTTTGAGGT[G/T]CGAGTCTCAGATTTC | 17974 |
rs33428237 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43509106 | ATGGGCAGGTGAATG[C/T]TTTTAGCCTTAGGAT | 17974 |
rs33428239 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43509139 | GGGATTCGGTTGGTG[A/G]CACCTGGGCACATGG | 17974 |
rs33428241 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43509169 | GCAATGCAAGAGACT[A/G]TCAGTTGTAGATAAG | 17974 |
rs33428465 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43505919 | ATTAGCCTCTTAAAA[A/G]ACTTCATTTGTTTTT | 17974 |
rs33428469 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43506926 | AAATGGTGTAGTGTT[G/T]CTTAGTAAGGTCACT | 17974 |
rs33428471 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Nck2 | Mm_Celera | 1:43506949 | AGGTCACTTGGGGAC[A/G]TAAAATTCCGCTTTT | 17974 |
rs33428715 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43527105 | CGAGCTTATGCTCAC[A/T]GATGGGTATTTCCAG | 17974 |
rs33428718 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43527138 | GCTTTTGTTTCTCTT[G/T]GCCCCATTATTGAGA | 17974 |
rs33428721 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43527195 | CTCTGTCTCAGGCCT[A/T]TGTTGTCCACAGTTT | 17974 |
rs33428723 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43527206 | GCCTTTGTTGTCCAC[A/G]GTTTATATAAAATTA | 17974 |
rs33428766 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43494103 | AATGAATATCCAGAT[A/G]TCTAGGAGAGTCTGT | 17974 |
rs33428769 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Nck2 | Mm_Celera | 1:43494150 | TTTCAGTTTATGACT[C/G]TGGCTTCACAGTGTC | 17974 |
rs33428772 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43494185 | GACACCTGAATCATA[C/T]CTGCTTTTTGGAGGA | 17974 |
rs33428804 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43482089 | CTACATAGTCTATAG[A/G]TACAGGATCTTTACA | 17974 |
rs33428806 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43482162 | TTGTCATCTTCTAAA[C/T]GTTGCAGTTACATTG | 17974 |
rs33428809 | snp | C/G/T | 0.46281 | 0.131194 | intron-variant | Nck2 | GRCm38.p3 | 1:43482258 | TGGGTTTTACGTAAG[C/G/T]GACTGGATTATGTGG | 17974 |
rs33428811 | snp | C/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43482288 | GGTCTTGGAACCTTT[C/G]GGGTAGAAGTCAATT | 17974 |
rs33428884 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43511908 | AGGGTGCGTTACACC[A/G]GCCAGGCAGTGATTT | 17974 |
rs33428886 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43511926 | CAGGCAGTGATTTCA[A/G]GGGCCATGTTTATTT | 17974 |
rs33428889 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43512144 | GGGCTGAGGCTCTTG[C/T]AGGACCAGTTAGATT | 17974 |
rs33428892 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43512430 | TAGGAAACACAATGG[C/T]TGGACAGCATCATCA | 17974 |
rs33428924 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nck2 | Mm_Celera | 1:43532266 | GGGTACAGTTGCTGA[A/G]GTAGGTGGTACCTCT | 17974 |
rs33428927 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Nck2 | Mm_Celera | 1:43532268 | GTACAGTTGCTGAGG[C/T]AGGTGGTACCTCTGT | 17974 |
rs33428929 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43532324 | CATCCCAGATTGACG[C/T]CATCGGATTTCTACT | 17974 |
rs33428931 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Nck2 | Mm_Celera | 1:43532395 | ACTGTTCAGGGGTTC[C/T]TACAACAGAGTTCTA | 17974 |
rs33428933 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43532698 | GCTCAAAGGAGACCC[C/T]ATGTCCAAATCCACC | 17974 |
rs33428955 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43502320 | TCAGAAAAGAGACAG[C/T]GGAGCATTTTCTAAC | 17974 |
rs33428958 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43502399 | TGCACTGGTTTGATC[C/T]CACAGTAGAGTCGAC | 17974 |
rs33428961 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43502424 | GTCGACTAGCGTTGG[A/G]TCCTGGGCTGGCAGG | 17974 |
rs33429204 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nck2 | Mm_Celera | 1:43537043 | CTTCTTGACATAGTA[C/T]GTATAAACATTTTAT | 17974 |
rs33429207 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43537135 | TTTTAGATTGGAAAG[C/T]GTCTCTTCTGTGGGG | 17974 |
rs33429210 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43537217 | TGATGTCATTCATGT[A/G]GGCTTTATACGGCTG | 17974 |
rs33429213 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Nck2 | Mm_Celera | 1:43537269 | GGGCCATGGTAGAAC[C/T]CCCATAGTTCATTCC | 17974 |
rs33429224 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43509330 | TTTACCTGCTACTCG[C/T]GCAGTATGAATGTGC | 17974 |
rs33429227 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43509586 | CTCAAACAAGCAAGC[A/G]CACTTAATATGTGTT | 17974 |
rs33429229 | snp | C/G | 0.124444 | 0.216185 | utr-variant-5-prime | Nck2 | Mm_Celera | 1:43509659 | GTGTCATCCCAGCTG[C/G]CTTAAGAGCTTGGAC | 17974 |
rs33429232 | snp | C/T | 0.124444 | 0.216185 | utr-variant-5-prime | Nck2 | Mm_Celera | 1:43509774 | CACCTCTTGTAACTG[C/T]GTGCCAAAGGTAAGC | 17974 |
rs33429346 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43541393 | CTTTCCAGACCTTGC[A/G]GCTCAACGTGGAACA | 17974 |
rs33429349 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43541433 | CAGTCATTGATTACT[C/T]GGGGATTCTGAACCC | 17974 |
rs33429352 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43541476 | GAAGGACAAAGAGAA[A/T]TGGAGAGACAGGAAA | 17974 |
rs33429384 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43553144 | ACACTCTTCAAAGTT[C/T]TTCTGCCTGGATTTA | 17974 |
rs33429387 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43553224 | AAAAGAGTTGAGTCT[A/T]TTGTGAGCAAAGCGG | 17974 |
rs33429390 | snp | C/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43553237 | CTTTTGTGAGCAAAG[C/G]GGTTGCAAATGGAGA | 17974 |
rs33429393 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43553276 | AGAAGGGCCAGCTTG[C/T]AGCCAGGCAATATGG | 17974 |
rs33429395 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43494189 | CCTGAATCATACCTG[C/T]TTTTTGGAGGACAGT | 17974 |
rs33429398 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43494343 | CCTTTTATGCACCAC[C/G]GTGTTGAGGCGCTGG | 17974 |
rs33429401 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43494608 | GCAGATGGAGCCCAC[C/T]TCAGACAGAGACTGT | 17974 |
rs33429403 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43494637 | GTAGTCCTAAAAAGA[A/G]CAATGCGTTGTAGAA | 17974 |
rs33429514 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43502820 | TGCATGGCATATACT[C/T]GGTTCACTCTATGCT | 17974 |
rs33429519 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43503049 | AAGAATAGTGTTAGC[A/T]CGATGACACTTGGGA | 17974 |
rs33429523 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43503371 | AAGCCAGGCTGTGTG[C/T]TCCTGTAATTCACTT | 17974 |
rs33429524 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43546184 | TTAGTCACATTACTT[A/T]CCAGCCTGCTAAGAA | 17974 |
rs33429527 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nck2 | Mm_Celera | 1:43546185 | TAGTCACATTACTTA[C/T]CAGCCTGCTAAGAAA | 17974 |
rs33429529 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Nck2 | Mm_Celera | 1:43546270 | GAAGAGGGACTGCCT[A/G]GGCACAAAGAAGACA | 17974 |
rs33429532 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43546331 | TACACCCTTTCTTCC[C/T]AGCCTTACCATTCAG | 17974 |
rs33429614 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43482312 | GTCAATTCCTTAAGT[C/T]AGTCGCTCATGGATG | 17974 |
rs33429615 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43482428 | GGGTTAAGCGATATG[G/T]GATACAGGACTTGTG | 17974 |
rs33429618 | snp | C/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43482494 | CAGATTTGTGTCCAG[C/G]CAGGGAGTTGAATAT | 17974 |
rs33429621 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43482524 | TGGTCTGAGAGTGTC[A/G]TTTAGAGTTTTAGGG | 17974 |
rs33429644 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43507002 | TAGGCATCTCCCTGA[A/G]TCACTCTCTGTAGTT | 17974 |
rs33429647 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43507100 | TGTATCAGGTGATTT[C/T]GTAATTTTTAGCCTT | 17974 |
rs33429649 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43507117 | TAATTTTTAGCCTTT[G/T]ACTTCATATGCCTTT | 17974 |
rs33429652 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43507183 | TTCTAGAAGGACCTC[C/T]AAGCCAAGTGGAAAG | 17974 |
rs33429775 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43527277 | AAGGCATGCAGTACA[C/T]AATACCCAGACTTTC | 17974 |
rs33429777 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43527348 | TAGGAAGGTGAGCAA[A/G]CTTGTGGCTAAAGTA | 17974 |
rs33429779 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43527654 | ATCATCCAATAATTC[C/T]AGAAAACAAACCACA | 17974 |
rs33429781 | snp | G/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43527761 | AGGAGACTTTGCCTC[G/T]CTCTAATAAAATGTT | 17974 |
rs33429785 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43512514 | GGCGGTCTTGGGTGT[A/G]TTCTCTAGTTAGTGG | 17974 |
rs33429788 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43512694 | AGACCTGGCGTGCCC[A/G]CTAGGAGAATGGAGA | 17974 |
rs33429791 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | Nck2 | Mm_Celera | 1:43512771 | CATGATCACTCTCAG[A/C]ATTTCACTTGGAAAC | 17974 |
rs33429793 | snp | A/C | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43512892 | TTCCCCAGTGTGTAG[A/C]GGCTGCTAGGATTAT | 17974 |
rs33429916 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Nck2 | Mm_Celera | 1:43537373 | GAGGAGATGGTGGTG[C/T]GGTGGGCCTTACCTC | 17974 |
rs33429919 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43537612 | AGTCAAGAAAAAATT[C/T]CCATGAAGAATAGGG | 17974 |
rs33429921 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43537727 | ATTACAACTTGATCT[A/G]TATAACTGAATAGGC | 17974 |
rs33429934 | snp | G/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43533122 | TTAGTAGTACATTAA[G/T]TGAATCTGAGTTTAA | 17974 |
rs33429937 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43533335 | CGTGCAGTGTGTTTA[A/G]TGCACTGAGAGGGGC | 17974 |
rs33429938 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43533369 | AGGCTTTGATTACAA[A/G]ATGTTGTTTCTCAGC | 17974 |
rs33429941 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43533399 | CAGCATTAGAGCTGA[C/T]GGGTAGGTCATTCTA | 17974 |
rs33429943 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43533444 | AAGGGGCTGGAAGGA[C/G]ACTGGTGGCAGTTGT | 17974 |
rs33430055 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43509811 | ATTTCTGCATAGAAG[A/C]GGCTTGGATGGTTTT | 17974 |
rs33430058 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43510151 | GAGCCATCTCCCCAG[A/G]TCCCTGCATAGTAGC | 17974 |
rs33430060 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Nck2 | Mm_Celera | 1:43510302 | GGTTTAGAATATTTA[A/G]ATAGAAGTAAGTATA | 17974 |
rs33430063 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43510361 | AGGGAGGTTCTGGAA[C/T]CTGTTCTGAGCAGAG | 17974 |
rs33430175 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43494695 | GAGAATTGAGGATTG[A/C]TGTTGCCCTTTTTGG | 17974 |
rs33430177 | snp | G/T | 0.297521 | 0.245442 | intron-variant | Nck2 | Mm_Celera | 1:43494826 | ACTCAAAATTAAAAT[G/T]ATAAATTCTTAGTTT | 17974 |
rs33430179 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43494882 | AAATAATAACTAGGT[A/G]TGTTTACATAATTAC | 17974 |
rs33430181 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43494962 | TTCAAGTAGCTATCA[A/G]TGTTACTGCTAACAA | 17974 |
rs33430255 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43541619 | ATGACTGTTAAGTAT[A/G]GAGAGCTCACGGCTT | 17974 |
rs33430258 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Nck2 | Mm_Celera | 1:43541676 | TACCTCAGACTGGTT[C/T]CTTTGTAAGGAAAAG | 17974 |
rs33430261 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43542092 | CTCCTCATGTATACT[A/G]GTGCTTATTCCCAGA | 17974 |
rs33430276 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43553396 | CTGGCCTAGATCTGG[C/T]CCACTGGAAAATTGC | 17974 |
rs33430278 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43553446 | TTAGTCCAACTTCTT[C/T]AGTCAGTCCCAGTGC | 17974 |
rs33430281 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43553574 | AGAAGGTTTTACTTT[C/T]CTCTCTTCTTGTTAT | 17974 |
rs33430454 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43546344 | CCTAGCCTTACCATT[C/T]AGCTCTGAACTTGGG | 17974 |
rs33430457 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nck2 | Mm_Celera | 1:43546367 | AACTTGGGAGTTTTA[C/T]ATGGCACTCGGTAGA | 17974 |
rs33430460 | snp | C/T | 0.5 | 0 | intron-variant | Nck2 | Mm_Celera | 1:43546476 | AGTGCAACCCCTTAT[C/T]GGCTGCACCTTCCCA | 17974 |
rs33430463 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Nck2 | Mm_Celera | 1:43546698 | ACCTGCAGGGAAGAA[A/G]TACATACAAGATGGC | 17974 |
rs33430585 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43507331 | CCATGTCTAGTCATC[A/C]GTCAGAGCCAAACTT | 17974 |
rs33430587 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43507351 | GAGCCAAACTTCTTT[C/T]CTCAAGATAATCTCT | 17974 |
rs33430590 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43507483 | ATGCCCCACCTCTGC[A/G]GGATGGACACCTTAG | 17974 |
rs33430592 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Nck2 | Mm_Celera | 1:43507612 | CATTGTAATGAATTA[A/G]CTATAAAAAGATTAT | 17974 |
rs33430593 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43507624 | TTAGCTATAAAAAGA[C/T]TATTATGCACAATGT | 17974 |
rs33430635 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43503380 | TGTGTGTTCCTGTAA[C/T]TCACTTTGACCCCTA | 17974 |
rs33430638 | snp | A/G/T | 0.244898 | 0.249948 | intron-variant | Nck2 | GRCm38.p3 | 1:43503463 | TGGCATCATTTTCAC[A/G/T]TGGCAGGCATGCAGT | 17974 |
rs33430641 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43503580 | TAAGTAGTAGCCTCA[A/G]CATCATATATACCTG | 17974 |
rs33430643 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43503607 | CCTGCAGGCTGTAGA[C/T]CAGGGATTTGTTTCC | 17974 |
rs33430736 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43512967 | CTCCTGCACAGGTAC[G/T]ACAGGACAGGAGACA | 17974 |
rs33430738 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43512995 | ACATTAACACACAAG[C/T]CTGCCAGTTACTCTT | 17974 |
rs33430741 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43513109 | CCAGCTTAACATCTC[A/G]CAGCCTGTTTTGTAT | 17974 |
rs33430814 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43528217 | CCATGCACTCCTTGA[C/T]GATGCAGATGGTACA | 17974 |
rs33430817 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43528273 | TATATATATTCTCTT[A/T]TATGTGTGGTGTGTT | 17974 |
rs33430820 | snp | A/C | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43528309 | GTTTTAGGAAGGTGG[A/C]GAGACCTTGCCTTTT | 17974 |
rs33430823 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43528397 | GTTAGGATTAAAGTG[C/T]ATTTGCTGTAATTAG | 17974 |
rs33430914 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43537750 | GAATAGGCCAGATAT[C/T]AGCCTTATGCTAAAA | 17974 |
rs33430917 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Nck2 | Mm_Celera | 1:43537856 | TTTGTTACCATTCTG[A/G]TTTTAGCTAGAACCC | 17974 |
rs33430919 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43537871 | GTTTTAGCTAGAACC[C/T]ACCACAGCCCCAAAG | 17974 |
rs33430921 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43537921 | TGACTACGAACAGTA[C/G]ACAAGTTAAGCAGAA | 17974 |
rs33430946 | snp | C/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43533494 | GACAATTTTTCAGAT[C/G]TGTCAGAGGAGAGGT | 17974 |
rs33430949 | snp | C/G/T | 0.244898 | 0.249948 | synonymous-codon | Nck2 | GRCm38.p3 | 1:43533699 | GCGGGTGAGGAATGC[C/G/T]GCCAACAGGACAGGC | 17974 |
rs33430952 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43533822 | CCCACAGGAACACTC[A/G]GGATAGCACTGTTGC | 17974 |
rs33430976 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43510484 | GATGAGTTCACATGA[C/G]TATTAAATTCAAACA | 17974 |
rs33430979 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43510546 | TATGAAAGATGTGTT[C/T]GAGCTATAATAAAAG | 17974 |
rs33430982 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43510901 | GCAGCTCATCCAGTG[C/T]TCCCTCTGGCTGACA | 17974 |
rs33431174 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nck2 | Mm_Celera | 1:43542133 | ATACATAGGTCTGGA[A/G]GCTAAGCCATGGAAC | 17974 |
rs33431177 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43542265 | GTACCTCAAGCCAGC[C/G]TTTCCATCATTTTCT | 17974 |
rs33431180 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43542428 | TCTTTGATTGCAGCT[A/G]ACTGAATAGTTAACA | 17974 |
rs33431183 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43542540 | AAAGGGGCTAGAGAA[C/T]TTTACAATAGCATGC | 17974 |
rs33431216 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43547741 | GTGGTTTCTAATGGC[C/T]TCTGGAGCCTCCTGC | 17974 |
rs33431219 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43547933 | CTCTGCTTCCTTCAG[A/G]CTTAAAAGCTACACA | 17974 |
rs33431222 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43548136 | ATTTTGGTTAAATTC[A/G]ATGTAGGTTACAGAT | 17974 |
rs33431224 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43495035 | TGTCTCACTAGGGAG[C/T]ATAGTCGGATTATTG | 17974 |
rs33431254 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nck2 | Mm_Celera | 1:43553819 | GGCATGGTGTACAAC[A/G]TATGTCCAGTGCCAG | 17974 |
rs33431257 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43553823 | TGGTGTACAACGTAT[A/G]TCCAGTGCCAGCTGA | 17974 |
rs33431260 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Nck2 | Mm_Celera | 1:43554096 | GCGTGGCAGCTTCAA[C/T]GGGCAGATCGGCTGG | 17974 |
rs33431263 | snp | C/T | 0.244898 | 0.249948 | synonymous-codon | Nck2 | Mm_Celera | 1:43554130 | CCCTCCAACTACGTT[C/T]TGGAGGAAGCGGACG | 17974 |
rs33431564 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43513156 | CAGAGGCTGGGAGAA[A/G]GAAGCTTACTTAGCT | 17974 |
rs33431567 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nck2 | Mm_Celera | 1:43513215 | ACCTTGCTGGCAGAG[C/T]CCAAGGCTGTGCAGG | 17974 |
rs33431569 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43513807 | GATCAGTACTTGGAC[A/G]ATGGTGTCTAATCCC | 17974 |
rs33431572 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Nck2 | Mm_Celera | 1:43525443 | TGAATCAAGCTCACA[A/G]CATAGCTCTTTACAC | 17974 |
rs33431656 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43507650 | AATGTAGGTAAATTC[A/T]TATTAAGGAATCAAT | 17974 |
rs33431658 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43507702 | GAGTTGTATTTGGTT[C/T]CTTTGGGGTGTGCTG | 17974 |
rs33431676 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43528432 | AGTGCTGCAAAAAGC[C/T]ACCAACTGGCCTTTC | 17974 |
rs33431679 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43528610 | GCTTTTGCAGATCAC[A/G]AATCAAGGACCAGGA | 17974 |
rs33431682 | snp | A/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43528683 | AGAAAAACTCCTCAC[A/T]GAGACCAGCTTCCTG | 17974 |
rs33431745 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43534230 | TTCCCCTCGTCTTAG[G/T]TGATAGGATATTTTA | 17974 |
rs33431748 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43534415 | TCACTGTAACAAGCT[A/G]CTTGAGGTTAGGTTA | 17974 |
rs33431751 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43534519 | CTTGGCAAATTTTCA[A/G]TGTGGTGTAAGTACA | 17974 |
rs33431815 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43510941 | ACCTTGTAAGAATGT[A/G]TATTGTCATCTGTAG | 17974 |
rs33431816 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43511025 | CACAAATCTCATATT[A/C]TTTCTGTCATTTAGA | 17974 |
rs33431818 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43511125 | ATTTCTATGCGAGTT[A/G]GAATTCTCTTTCATT | 17974 |
rs33431821 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43511245 | TGCCTGGTACAATAA[G/T]TGCTGTTTGCAGTGT | 17974 |
rs33431904 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43537938 | CAAGTTAAGCAGAAG[C/G]ACTGTGGCCTCTGAA | 17974 |
rs33431906 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43538036 | GAAAGGCAGAGGTCA[A/T]GAGTCAGACATACCC | 17974 |
rs33431909 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43538551 | GGCATCTCACGTTTT[C/T]AACATTAGGACTACA | 17974 |
rs33431912 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Nck2 | Mm_Celera | 1:43538663 | TTGGCTGGAATGGTC[C/T]CCTGTGAGAACTGTA | 17974 |
rs33431995 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43548186 | GTTGTTGGCATCTGT[C/T]CTTTGAGTCTTCACG | 17974 |
rs33431998 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43548377 | TAGCTCAGTGCTTTG[A/G]TGGTTATTGAGAGCA | 17974 |
rs33432001 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43548635 | ATCCCACTTCCACCA[C/G]CCTGTCAACATCTGA | 17974 |
rs33432126 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43554636 | CAGAAGGAAGCTAAA[C/T]GCGCAGTTCCCTGAC | 17974 |
rs33432129 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43554742 | CATTGTTAAATGTCT[C/T]ACCAAGTCATGTAAG | 17974 |
rs33432132 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43554892 | CCGTGACTGGTAACC[A/G]TTCCCATGGCATGTT | 17974 |
rs33432136 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43542557 | TTACAATAGCATGCA[C/G]GAGCTGATACACAGG | 17974 |
rs33432139 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43542559 | ACAATAGCATGCAGG[A/G]GCTGATACACAGGTG | 17974 |
rs33432142 | snp | A/G/T | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43542604 | AGTTGGGCATTGTGC[A/G/T]GTCGGTCGCTCTGAA | 17974 |
rs33432386 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43557245 | CAACCAGCACTTGTG[A/C]ACTAACTCTGCCCAA | 17974 |
rs33432389 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nck2 | Mm_Celera | 1:43557398 | GATAAGTGTCAGTGT[C/T]TTATTTTCTGGATCC | 17974 |
rs33432392 | snp | G/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43557581 | GGTGCATTATGTGCC[G/T]TGATAATTATTAGGT | 17974 |
rs33432515 | snp | C/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43528859 | CAACTGTCTTTTCTG[C/G]TGTCTGGAGACATCT | 17974 |
rs33432517 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Nck2 | Mm_Celera | 1:43528948 | AGGATGATTGTAGCT[A/G]TCCAGAGCCTGCTGG | 17974 |
rs33432520 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43529119 | GTGAGTTTTTGTGAG[C/T]TGATAGTTGCTATCT | 17974 |
rs33432523 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43529130 | TGAGTTGATAGTTGC[A/T]ATCTTCCACCATCTA | 17974 |
rs33432584 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43525489 | CCCAGGAGCTAGCCA[A/G]AAGTAGCATACAAGT | 17974 |
rs33432587 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43525527 | TATTTCTGCCTTATT[A/G]TCACCAAAAGAGGAA | 17974 |
rs33432590 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43525656 | TAATGAGCTTGGAGC[G/T]GCTTGTGTGGTATTT | 17974 |
rs33432593 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43525668 | AGCTGCTTGTGTGGT[A/G]TTTAGAAAGCAAAAC | 17974 |
rs33432596 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43534552 | CTGGCAAGAGACTAG[A/G]GGAGATAGAGAATTG | 17974 |
rs33432599 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Nck2 | Mm_Celera | 1:43534798 | GGCAACCACACCTGA[A/G]TGTGCACAGCGTGCT | 17974 |
rs33432602 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Nck2 | Mm_Celera | 1:43534889 | GGACAGCTGAACTGA[A/G]CTGACAGTTTACAAT | 17974 |
rs33432764 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43548669 | GCGTTACTGGTGTAG[G/T]TGGGTATCTGTAGGA | 17974 |
rs33432767 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43548738 | GACTTTGCCTAAAAT[C/T]GGTTTGTGTTCAATT | 17974 |
rs33432769 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43548868 | TAGCTTGCAGAACAC[A/G]GGCTGCTTTGTGAGG | 17974 |
rs33432771 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43549115 | CTTGTGCACAGACAG[A/C]ACTTTGACAAATAGG | 17974 |
rs33432784 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43568648 | TAAGTAAGGCACTGA[G/T]CTCATCACAGAATTT | 17974 |
rs33432787 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43569013 | GCAGAATTTCATTAG[C/T]GCTTGATTGTGAGCC | 17974 |
rs33432790 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43569038 | TGAGCCTGAGAGCGC[C/T]GGGCTGCCAGTCAGT | 17974 |
rs33432792 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Nck2 | Mm_Celera | 1:43569442 | CTCCACCCATGTGGC[C/T]TGGATCACCTCTGTG | 17974 |
rs33432944 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nck2 | Mm_Celera | 1:43538882 | ACACTTATCTGATGA[A/G]TGAACATGGAACAGC | 17974 |
rs33432946 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43538913 | TTTCAAGTCTCACCG[C/T]ACTCTACCCTTGCCA | 17974 |
rs33432948 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43538950 | CTTACCGCACATACA[C/T]ATTTCCTGTCAACAG | 17974 |
rs33432951 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43539274 | TGCAGTAGATTGGAA[A/G]CTGTCTCTAAGTCAG | 17974 |
rs33432974 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43554945 | AAAATGGTATTTGAG[A/G]GCACGTACTAAAGTA | 17974 |
rs33432977 | snp | C/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43554958 | AGGGCACGTACTAAA[C/G]TAGCCAAATACTATG | 17974 |
rs33432980 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43555163 | GTTCTGTCCTGGTTC[C/T]GGCCTGTGTAGAAAA | 17974 |
rs33432983 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43555196 | CCTGTGATTACTTGT[G/T]CAATGCCCTGTGCAT | 17974 |
rs33433044 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43542690 | GCTTTTCAGAGAATG[A/G]TCAGCAAGGGCTTCA | 17974 |
rs33433047 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43543130 | TCTTGGTTCTTTGGA[A/G]TGCTTGAGGTTTTTA | 17974 |
rs33433050 | snp | A/G | 0.5 | 0 | intron-variant | Nck2 | Mm_Celera | 1:43543180 | GATTTGTGGCAGTGC[A/G]TTTGCTGTAGAAGTC | 17974 |
rs33433053 | snp | A/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43543243 | GCCATCTTGCCTTAG[A/T]ACATGATTCCTAGCC | 17974 |
rs33433244 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Nck2 | Mm_Celera | 1:43511346 | TTCCTGTGGAGAGAG[A/T]GGCTCATTGTCCCGC | 17974 |
rs33433247 | snp | C/G | 0.396694 | 0.202437 | intron-variant | Nck2 | Mm_Celera | 1:43511361 | AGGCTCATTGTCCCG[C/G]GTATGCGGGGTGTGT | 17974 |
rs33433325 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Nck2 | Mm_Celera | 1:43557591 | GTGCCTTGATAATTA[C/T]TAGGTACTGATATTT | 17974 |
rs33433328 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43557603 | TTATTAGGTACTGAT[A/G]TTTGTCATGCGTCAC | 17974 |
rs33433331 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43557611 | TACTGATATTTGTCA[C/T]GCGTCACACTCATTT | 17974 |
rs33433355 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Nck2 | Mm_Celera | 1:43535069 | TTGGAGGGGGCAGGG[A/T]GAAGGAAATATGGGG | 17974 |
rs33433358 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43535248 | CAGAATGTGTGTGGC[A/T]AATGTAGACGCTGAG | 17974 |
rs33433361 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Nck2 | Mm_Celera | 1:43535408 | TCTTAGTTAAGTATG[A/G]TAAATAAAGAAGATG | 17974 |
rs33433363 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43535703 | CAGATTTCCCTGAGT[G/T]CGATCAGTTCCTCTT | 17974 |
rs33433386 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43525767 | CCTGGCAGCTGCAGG[C/T]GACAAGTGATCAAGG | 17974 |
rs33433389 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Nck2 | Mm_Celera | 1:43526204 | ATTTCTTAGATTATA[A/G]GTGTCTTTCTGTAGC | 17974 |
rs33433392 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Nck2 | Mm_Celera | 1:43526234 | CAGTGACAAAATACC[A/G]GAGGGCACATGTAAG | 17974 |
rs33433426 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Nck2 | Mm_Celera | 1:43529178 | TAGAAAAAAATATTC[C/T]AGAGACCTTCCATGA | 17974 |
rs33433428 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43529242 | TTGAAAATTGGCATT[A/G]GGATGGCATCTGTCT | 17974 |
rs33433431 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nck2 | Mm_Celera | 1:43529492 | TTTAGATTGGCAGTC[C/T]TCCAATAGTTAATCT | 17974 |
rs33433585 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nck2 | Mm_Celera | 1:43562024 | CTTCCATACCATTAA[A/G]AGGGCCATCCTGAAG | 17974 |
rs33433588 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43562102 | TTATGGACTTCGCAT[C/G]CACAGAGAATAAAGA | 17974 |
rs33433591 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43562155 | ACAGTTAGCTTTATA[A/G]CCACTTTCACAGTTT | 17974 |
rs33433724 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43549204 | TGTTTTATTTTCTCT[A/G]GACTCTCAATTGATG | 17974 |
rs33433725 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43549502 | AACCCAGGTGGAAAA[A/G]CCTTGACTATGAAAG | 17974 |
rs33433727 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43549523 | ACTATGAAAGGGTTA[A/G]GAAGTGTTGACCAGG | 17974 |
rs33433730 | snp | A/G | 0.5 | 0 | intron-variant | Nck2 | Mm_Celera | 1:43549731 | CCCTGCTGTAGAGGA[A/G]CACAGCTTATTGACT | 17974 |
rs33433733 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Nck2 | Mm_Celera | 1:43550061 | AAGTCAGCACACAGT[C/G]ATGTGAAATCACTCA | 17974 |
rs33433746 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Nck2 | Mm_Celera | 1:43555271 | ACACAGCCTTGTGTT[A/G]CTGGTTTGTAAACTG | 17974 |
rs33433749 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Nck2 | Mm_Celera | 1:43555592 | TTTAGTCCAGTATCT[G/T]TAAGTGTTACCAGTT | 17974 |
rs33433752 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Nck2 | Mm_Celera | 1:43555597 | TCCAGTATCTGTAAG[G/T]GTTACCAGTTCTCCC | 17974 |
rs33433774 | snp | A/C | 0.142012 | 0.225474 | utr-variant-3-prime | Nck2 | Mm_Celera | 1:43569749 | CCGAGAGCTGTGTCC[A/C]TGGGTGTTTGGTGCC | 17974 |
rs33433776 | snp | A/G/T | 0.231111 | 0.249285 | utr-variant-3-prime | Nck2 | GRCm38.p3 | 1:43570009 | AAAGAGGGTTTTGGT[A/G/T]AGAGTTGGTCTGCAA | 17974 |
rs33433778 | snp | A/G | 0.132653 | 0.220748 | utr-variant-3-prime | Nck2 | Mm_Celera | 1:43570021 | GGTAAGAGTTGGTCT[A/G]CAAAAGAGGAAGGTG | 17974 |
rs33433781 | snp | C/T | 0.142012 | 0.225474 | utr-variant-3-prime | Nck2 | Mm_Celera | 1:43570461 | AGGGGTCTTGGGATC[C/T]CCTAAACTTGCATAC | 17974 |
rs33433836 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43543425 | TCATTACTATCTACC[A/C]TTGTGCACGTATGAG | 17974 |
rs33433839 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Nck2 | Mm_Celera | 1:43543614 | ATTTGTTTTTGTATC[A/T]CATGCATTTCCAAGT | 17974 |
rs33433842 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Nck2 | Mm_Celera | 1:43543840 | GCCCACTAGGCTGCC[G/T]TAGCCCCTTGTGTCT | 17974 |
rs33433924 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43539459 | TTTGTAGTACTGGGG[C/T]AATGGAATATGGTCT | 17974 |
rs33433927 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43539610 | ACCCCCAGCTCTGTA[A/G]GAACATTTGCAGCAG | 17974 |
rs33433929 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43539771 | GTCCTGCTTGATTTG[C/G]AATTTCCTGAAGTCA | 17974 |
rs33433932 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Nck2 | Mm_Celera | 1:43539939 | GTGAGGGTGTGTCCG[C/T]GGTAGTCTTCCTGCT | 17974 |
rs33434174 | snp | A/T | 0.297521 | 0.245442 | intron-variant | Nck2 | Mm_Celera | 1:43557656 | GTCCTTTGATAAAGA[A/T]GATTTAATATTTTAT | 17974 |
rs33434177 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43557979 | AGTCATCGTTCCGGA[C/T]CAAAATCATTTTATT | 17974 |
rs33434180 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Nck2 | Mm_Celera | 1:43558028 | GACCATAGTTTAAGA[A/G]TAAGAATAATGGGTT | 17974 |
rs33434183 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nck2 | Mm_Celera | 1:43558138 | TATAACGCAGTTCAG[A/G]TCCAGATGCCCTCAG | 17974 |
rs33434185 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43535729 | CTCTTGTTTCACAAC[C/T]CTAGTTACAGAGCAA | 17974 |
rs33434188 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43535999 | ACAGCTCTTCTGTGA[A/G]CTTCTGTCTCAGCTT | 17974 |
rs33434191 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43536012 | GAGCTTCTGTCTCAG[C/T]TTCAACACATCGTTC | 17974 |
rs33434205 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43526573 | AGATGTGTGCAAGTC[A/G]GCCTGTGGTAGCTCA | 17974 |
rs33434207 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43526736 | TAGACAGATGCTTAG[A/G]AATGTGGTATCATCA | 17974 |
rs33434208 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43526763 | ATCATTTAAACACAC[G/T]GAGCCAAGGTGACCT | 17974 |
rs33434364 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Nck2 | Mm_Celera | 1:43529516 | TTAATCTTTATTAAG[A/G]CCTTTTTAATCATTA | 17974 |
rs33434367 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nck2 | Mm_Celera | 1:43529559 | TCAATGTTGTTATTA[C/T]TCTTTTTAAAATAGT | 17974 |
rs33434370 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43529671 | CTCATGTAACTTCCA[A/G]TTTTCCTCCTTTTCT | 17974 |
rs33434373 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43529853 | AAGAGATGCTTTCCA[A/G]AATGGGGTCTGTTCT | 17974 |
rs33434444 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43562187 | GCCTTGTGCCTACAT[C/T]CCGTCCACAGCATGG | 17974 |
rs33434446 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43562226 | CCATCTGCTCCAGAG[C/T]GGCATAGTGGCTCCA | 17974 |
rs33434449 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43562346 | CTTGATGCTGGGGCC[A/G]TCTCTCAACTTTTTT | 17974 |
rs33434451 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43562354 | TGGGGCCGTCTCTCA[A/G]CTTTTTTCTGGTCCC | 17974 |
rs33434565 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nck2 | Mm_Celera | 1:43555698 | TGAGCAGTGTACACA[A/G]AACCGATCTGAGAGG | 17974 |
rs33434568 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43555869 | GTCTCTGAATGCTGA[C/T]TGCCTCTGAAATCTG | 17974 |
rs33434571 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Nck2 | Mm_Celera | 1:43556005 | GGTCACATTCTGGGC[C/T]CGTGAGGACAGCACC | 17974 |
rs33434635 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43543886 | GGTCAGATTCATTAC[C/T]GTGAGTCCCTGTCTC | 17974 |
rs33434638 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Nck2 | Mm_Celera | 1:43544387 | TTCCCCATATGGCCT[G/T]CATCTTTGTTAGCTT | 17974 |
rs33434640 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43544487 | CATTGCTACCTGGCA[C/G]CATGCGGCTGTACGG | 17974 |
rs33434642 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Nck2 | Mm_Celera | 1:43544509 | GCTGTACGGACTGCT[A/G]AACTCCCCATACTGC | 17974 |
rs33434744 | snp | G/T | 0.231111 | 0.249285 | downstream-variant-500B | Nck2 | Mm_Celera | 1:43570825 | GGATGCATGTGAACG[G/T]GTGCACATTCACACA | 17974 |
rs33434747 | snp | C/T | 0.231111 | 0.249285 | downstream-variant-500B | Nck2 | Mm_Celera | 1:43570852 | CACATCACTGGCACA[C/T]AAATGAGAGCTCTCA | 17974 |
rs33434796 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Nck2 | Mm_Celera | 1:43550656 | AATGTAGCTCAGGGC[C/T]AGAGAGCTAACACCT | 17974 |
rs33434799 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43550996 | ACCTGTGTCAACTGC[A/G]TAGTGTTGGTTGCTC | 17974 |
rs33434802 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43551030 | TGCTTAGGGCTCTGT[A/G]GAGAGGAAACAGCAT | 17974 |
rs33434804 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43536427 | ATGATCACCTTTGCC[A/G]TTGGACAAAGAGAGA | 17974 |
rs33434807 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Nck2 | Mm_Celera | 1:43536455 | AGACCTGGTTATCTT[A/G]AGTACAGGCTTCCTG | 17974 |
rs33434855 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Nck2 | Mm_Celera | 1:43539972 | TAGCTCTCAGCTCCC[A/G]TGGTTGTGAGGAGAC | 17974 |
rs33434858 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Nck2 | Mm_Celera | 1:43540001 | ACTTATCAAGTTCTC[A/G]TTTAGGCATCAGAAC | 17974 |
rs33434861 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43540095 | GGGAGAACCTGGGAG[A/G]TGAATTCAGCAGCCT | 17974 |
rs33435096 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nck2 | Mm_Celera | 1:43558207 | CGGCATTTCTCAGAA[C/T]GAAAGGTCTTTCTGG | 17974 |
rs33435099 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43558262 | CAAGTCATTTCCTTA[C/G]GGTTTGCATCGTCCA | 17974 |
rs33435102 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43558272 | CCTTAGGGTTTGCAT[C/T]GTCCAGCTTCCTAGC | 17974 |
rs33435106 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43529916 | CCATATCAGAATTTA[A/G]TTCCCATGCCAGGGC | 17974 |
rs33435109 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Nck2 | Mm_Celera | 1:43531022 | AAAATTACCCACTAC[A/G]TCCTTGTGCCTCATT | 17974 |
rs33435384 | snp | A/C | 0.497041 | 0.0383476 | intron-variant | Nck2 | Mm_Celera | 1:43556423 | TGTGGGGCCTCTCTG[A/C]CCCTACATTCTTGGG | 17974 |
rs33435387 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43556508 | ACTGATGAAAGAACG[A/G]GCCAGATTCAGGTTT | 17974 |
rs33435390 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43556606 | TTTGGGATTTTTCAG[A/G]TCAGAGCCTTGTCCT | 17974 |
rs33435393 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Nck2 | Mm_Celera | 1:43556840 | TACATCTTCCTGATA[C/T]GTATCTCAGGTGATT | 17974 |
rs33435464 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Nck2 | Mm_Celera | 1:43563231 | CCTGACAGGAGCAGC[A/G]AAGTTAGAAGTAGCG | 17974 |
rs33435466 | snp | C/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43563329 | TTCACCTTCCTTGCT[C/G]TACTCGGTTTCGCTT | 17974 |
rs33435469 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Nck2 | Mm_Celera | 1:43563412 | CTGCCGGAGCTCAGA[A/G]GCAGTACTTCTTAGA | 17974 |
rs33435472 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Nck2 | Mm_Celera | 1:43563506 | TGAATCTGATGCTGG[A/G]ACTTGAAGTCCTGCC | 17974 |
rs33435525 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43544543 | GAGTCCCTACTGGTT[C/G]TTGCTTTCCTCTGGC | 17974 |
rs33435528 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nck2 | Mm_Celera | 1:43544674 | ATGCTAGGCCCTATG[C/T]TACCATCAGCCAAGG | 17974 |
rs33435531 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nck2 | Mm_Celera | 1:43544962 | TCACAGGTTTTCCAA[A/G]TGCACTCGGGTGGTG | 17974 |
rs33435655 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43551279 | GCCTCAAAATGAAGG[A/G]CTAGGGAAACTTGTT | 17974 |
rs33435658 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43551628 | CAGATCTTCAGTTTA[G/T]GTGTGAAAATCTTGC | 17974 |
rs33435661 | snp | A/T | 0.345679 | 0.230967 | intron-variant | Nck2 | Mm_Celera | 1:43551691 | GTTTTGTTTAGGGAT[A/T]TTATTATTATTATTA | 17974 |
rs33435704 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43540167 | CATCCCTTCTAAGCC[A/G]CTGTATTTCCTGCAA | 17974 |
rs33435707 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43540278 | TTCAGTAAGGATGAC[A/G]TGATGAGATATGGTC | 17974 |
rs33435710 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43540433 | TAGGACTGAATTGGG[C/T]AGCTTGGCAACCATC | 17974 |
rs33435713 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43540469 | TGAGTAGAAGGGAGA[C/T]TCTAGAGCAGTGGTT | 17974 |
rs33435905 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43558277 | GGGTTTGCATCGTCC[A/C]GCTTCCTAGCCAAGT | 17974 |
rs33435908 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43558304 | AAGTTGGCATTAGGA[A/G]TAAGCAGGTTACCCA | 17974 |
rs33435910 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Nck2 | Mm_Celera | 1:43558744 | GGAAAAAGTCATTTT[C/G]TCAGGCTTTTTGTAT | 17974 |
rs33435913 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43560019 | TTAGAAGGCTATATA[C/T]GTTTAGAATGGGCTC | 17974 |
rs33436166 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Nck2 | Mm_Celera | 1:43556841 | ACATCTTCCTGATAC[A/G]TATCTCAGGTGATTA | 17974 |
rs33436169 | snp | C/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43556894 | AGATGGTGTTGTGCA[C/G]TGATAAATGCCTGCT | 17974 |
rs33436172 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43557017 | AAGCATTGTTTCATC[G/T]GTGCCTTCCAGGCTG | 17974 |
rs33436395 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Nck2 | Mm_Celera | 1:43564120 | ACACAGAAGATGTTA[A/C]TCAGTAGTGCCCATT | 17974 |
rs33436398 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43564304 | GAGATGCAGGGAATA[A/T]CAACATTAGTGCAGA | 17974 |
rs33436400 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43564377 | ATGTGGGTGGTCAAG[A/G]ACATTTCTTGTCCAA | 17974 |
rs33436402 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43564654 | AGAGGCACTTTTGAG[A/G]TTTTTAAACTGGGTC | 17974 |
rs33436434 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43545014 | GTGGTGGTGGTGTTT[C/T]CCAGCTTTGGAATCG | 17974 |
rs33436437 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43545065 | CCAATTTTTGAGGCC[A/G]TACCAACTGTGTTTC | 17974 |
rs33436439 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nck2 | Mm_Celera | 1:43545106 | CTTGCATGAGTAAAT[A/G]GCTGTTTGCAGGCAA | 17974 |
rs33436442 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Nck2 | Mm_Celera | 1:43545319 | CCAGAATTGCAAGTA[A/G]TCTGTCCAGCTACCC | 17974 |
rs33436464 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Nck2 | Mm_Celera | 1:43552130 | AAGTCTCACACCCTA[A/G]GTCAGTTTTGTAAGG | 17974 |
rs33436467 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43552216 | ATGCAGATTGGTACA[A/G]ATTCTCCAGTGTGCA | 17974 |
rs33436470 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Nck2 | Mm_Celera | 1:43552396 | TGGAAAGTACTTGTC[C/T]CTATATGTGGTATAG | 17974 |
rs33436473 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43552545 | TCTTTTGATAAAATA[C/T]GTCAAATTCTAGGAG | 17974 |
rs33436585 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Nck2 | Mm_Celera | 1:43541113 | GGACTGGACTGAGTC[A/G]GACCAGGCACTGGCC | 17974 |
rs33436588 | snp | A/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43541207 | ATAGAGGTTACGTTT[A/T]TATGGATGGTAGATA | 17974 |
rs33436591 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck2 | Mm_Celera | 1:43541290 | AGGCTGGAAACAGGG[C/T]CTCAACATGACCCAT | 17974 |
rs33436786 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Nck2 | Mm_Celera | 1:43560092 | AGCCAGAGCCCTTGG[A/C]GGCAGATTCCTCTTC | 17974 |
rs33436788 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Nck2 | Mm_Celera | 1:43560203 | GAGGCTAGCTCTTAC[A/G]CAAAGACGGCTCATC | 17974 |
rs33436791 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nck2 | Mm_Celera | 1:43560397 | TCTGTGAGTTGAGTC[A/G]TCCAAGCCAACAGTG | 17974 |
rs33436964 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43557038 | TTCCAGGCTGGGAGA[A/G]TGCTAAGCATTGCAG | 17974 |
rs33436967 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43557077 | GTACTGGACTTGAGA[A/G]ACAAACAAGCAGACC | 17974 |
rs33436970 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43557100 | AGCAGACCTGTTTGA[C/T]TCAACCACCCCCAAC | 17974 |
rs33437424 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43545901 | ACAGTCTTAGATAGC[G/T]AAGGTGTTTTGCTGG | 17974 |
rs33437427 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43546020 | GCTCTTGGATTGGGT[A/G]CATGTGTTGAGAGAT | 17974 |
rs33437494 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Nck2 | Mm_Celera | 1:43541340 | GAGCTCAGTAGTGAG[A/C]ATGGAGAAGCTCATT | 17974 |
rs33437504 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43564688 | CAGGTACCTCTGTAG[A/G]AACCATCTGACTCTG | 17974 |
rs33437506 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43564710 | CTGACTCTGTAGAAA[A/G]CACCAGTGAGCATCT | 17974 |
rs33437509 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43564756 | AAAAATACCTATACA[C/T]AAAAATTGCTGAGAT | 17974 |
rs33437644 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Nck2 | Mm_Celera | 1:43560455 | ATTAACCTGGAGGTG[G/T]CCTCTCAGTTACCTC | 17974 |
rs33437647 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Nck2 | Mm_Celera | 1:43560476 | CAGTTACCTCAGCAG[A/T]GTGTCTCGCTCCCAC | 17974 |
rs33437650 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nck2 | Mm_Celera | 1:43560729 | GAGAGTTAGCCCAAG[A/G]TTATATTAGGAACAT | 17974 |
rs33437653 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43561006 | GGGAGAGGAGGCCAT[C/T]CCCTGTCCGCTAAAG | 17974 |
rs33438476 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck2 | Mm_Celera | 1:43561068 | TTGACAGTTCAACCT[C/T]AAGAGTGTTCAGAAG | 17974 |
rs33438478 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Nck2 | Mm_Celera | 1:43561102 | TCTCATTCAAATCCC[A/T]TAGATCTGTAGCTCC | 17974 |
rs33438481 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Nck2 | Mm_Celera | 1:43561137 | TGCAAAAAGACTTAT[A/G]TAGAGTTCTTGCAAA | 17974 |
rs33438655 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43565143 | CAGTGCTGGGAGAAC[C/T]TGTGGAGCCCAGGGA | 17974 |
rs33438658 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43566017 | GTAGACTACGAGGAA[A/C]GTTGGCCGTAAGCCA | 17974 |
rs33438661 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43566080 | TTCCCATCTTTTCTG[G/T]CTACTTATACATCTA | 17974 |
rs33438663 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43566240 | CCTCTCTTCATAAAG[A/T]CCCCATAAAGATGAC | 17974 |
rs33439434 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Nck2 | Mm_Celera | 1:43561202 | AAATATGTATGTAAA[A/C]GTATAATGGAAAGAG | 17974 |
rs33439437 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43561427 | CATATGGAGACTTTC[A/G]TTTACTTCTCAGAGA | 17974 |
rs33439440 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Nck2 | Mm_Celera | 1:43561431 | TGGAGACTTTCATTT[A/G]CTTCTCAGAGAAAGG | 17974 |
rs33439443 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43561505 | TATGTAAAGTTAGTC[C/T]TGATATGAAACTATA | 17974 |
rs33439806 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43566627 | CACATTGTATTGAGA[A/G]GCAATAGGGTCCTGT | 17974 |
rs33439809 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43566697 | AATTTGAATTAAGAA[C/T]GCTCGAGACTCCTGC | 17974 |
rs33439812 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43566838 | CCTTACATGTCATGG[G/T]ATCATATTAAGGATT | 17974 |
rs33440265 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Nck2 | Mm_Celera | 1:43561562 | AATAAAACACGTGTA[C/G]AGCAGACTAAGGACA | 17974 |
rs33440268 | snp | A/C/T | 0.231111 | 0.249285 | intron-variant | Nck2 | GRCm38.p3 | 1:43561942 | AAAGGAACTCGCAGA[A/C/T]AAAATCATCATACAG | 17974 |
rs33440495 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43567222 | TAAGTAGCATCTGTT[A/G]TTCACTTCCCACGTG | 17974 |
rs33440498 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43567451 | GGATCTTGGGGCGTG[A/G]AAAGGTCTGTCTGTT | 17974 |
rs33440501 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Nck2 | Mm_Celera | 1:43567894 | ATTAGCAGCAAGTTC[C/G]CAGGGATAGGAGCAA | 17974 |
rs33441264 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43567916 | TAGGAGCAAGCAGGA[A/G]CAGACTTAGAAGGGC | 17974 |
rs33441266 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Nck2 | Mm_Celera | 1:43568001 | CCTGCCCAGGCAACT[A/C]GACTTTTGAGAATAG | 17974 |
rs45683222 | snp | A/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43450437 | GAGATTACACTCAGG[A/T]ATATACTATATATGA | 17974 |
rs45756814 | snp | A/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43491273 | CCTGTGAAAGGGGCA[A/T]TCAACCTCTCCTGGG | 17974 |
rs45801216 | snp | C/T | | | intron-variant | Nck2 | Mm_Celera | 1:43480013 | GTTTGTGCCCCTCTG[C/T]ATCCTGTAGGCAGTC | 17974 |
rs45818805 | snp | A/G | | | intron-variant | Nck2 | Mm_Celera | 1:43515352 | GTGGGGAAAAGCCTC[A/G]AATTCATTGGCACAG | 17974 |
rs45829655 | snp | C/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43447524 | TTTGATTGAAGAACG[C/T]AAAGGTCCCAGTGAC | 17974 |
rs45897901 | snp | C/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43449915 | CTGGTCTGCAAATTT[C/T]GTGACTTCATTTTTC | 17974 |
rs45962324 | snp | A/G | | | intron-variant | Nck2 | Mm_Celera | 1:43503813 | TTTGCTTGGGATAAA[A/G]ATGGAGCAACATCCT | 17974 |
rs46002950 | snp | C/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43450407 | TTGTCCAAATTCAAG[C/T]GGACTAGAAATACTG | 17974 |
rs46097821 | snp | A/G | | | intron-variant | Nck2 | GRCm38.p3 | 1:43492157 | CCACTTGTTCCTGTG[A/G]CCACAGAACTGGGTT | 17974 |
rs46126743 | snp | A/C | | | intron-variant | Nck2 | Mm_Celera | 1:43483970 | GTAAATGCAAGGAGG[A/C]GAAGAAGAGCAAATC | 17974 |
rs46127070 | snp | G/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43481412 | TTCCTCCTCATTTTG[G/T]TTTTTTCTTCCCATA | 17974 |
rs46230541 | snp | G/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43450378 | GCATATTCCACCCCT[G/T]ACCTTGTGACAAATT | 17974 |
rs46311130 | snp | A/T | | | intron-variant | Nck2 | Mm_Celera | 1:43515402 | AACTCCAGTGGCTCA[A/T]GCTCTAAGAGCCATT | 17974 |
rs46314488 | snp | C/T | | | intron-variant | Nck2 | Mm_Celera | 1:43503714 | TTTTGTTCGTTTCCT[C/T]TTCTTGGCTCTAACC | 17974 |
rs46318580 | snp | G/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43447965 | CTAAATCTCTCCAGA[G/T]CTTTCCTTGTTGGAG | 17974 |
rs46773961 | snp | C/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43447621 | TCTCAGTTTCTTACA[C/T]GTGCTTGAACAGAGC | 17974 |
rs46790624 | snp | A/G | | | intron-variant | Nck2 | GRCm38.p3 | 1:43448249 | AGAGCAGTGTAGGGA[A/G]CAGTGGTTGGGGAAA | 17974 |
rs46823670 | snp | A/G | | | intron-variant | Nck2 | GRCm38.p3 | 1:43448988 | ACTTGTGAGTAGCCA[A/G]AGGTCCCTTTCCCAG | 17974 |
rs46835625 | snp | A/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43462979 | CGGCAAATCAGGAAC[A/T]CTCTTCTCTGAAAAG | 17974 |
rs46841679 | snp | A/G | | | intron-variant | Nck2 | Mm_Celera | 1:43503912 | CCTAGTGTAACCTGT[A/G]GATATTCTGCTTTGC | 17974 |
rs46860537 | snp | A/C | | | intron-variant | Nck2 | Mm_Celera | 1:43467796 | ACTGTGTTTTTTTCG[A/C]TCTTTCTGGAAGAAG | 17974 |
rs46879347 | snp | C/G | | | intron-variant | Nck2 | GRCm38.p3 | 1:43450946 | AGCAAGCAGGTGAGG[C/G]TTACTGAGTCCCAGA | 17974 |
rs46895192 | snp | A/C | | | intron-variant | Nck2 | Mm_Celera | 1:43515659 | GTCTTACTGTTCTTG[A/C]TAACACTTTGAGTAA | 17974 |
rs47034939 | snp | A/G | | | intron-variant | Nck2 | Mm_Celera | 1:43511195 | TTGATGCTTTTTAAA[A/G]CACTTGTCTAGAAAC | 17974 |
rs47038133 | snp | G/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43481470 | AGGCTAGGCAAACAC[G/T]GCCACTGAGCTACAT | 17974 |
rs47044223 | snp | A/C | | | intron-variant | Nck2 | Mm_Celera | 1:43486018 | ATTTTCTCGCCCCCC[A/C]CCCCCCCCCCCCATC | 17974 |
rs47072459 | snp | C/T | | | intron-variant | Nck2 | Mm_Celera | 1:43505305 | GTAGGCCCAACAGCA[C/T]TGGAGAGGGTGATGT | 17974 |
rs47131591 | snp | A/G | | | intron-variant | Nck2 | Mm_Celera | 1:43447403 | GAACACAATGGAGAA[A/G]GTGCACTTTAGACAG | 17974 |
rs47146426 | snp | C/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43461836 | CTCGTTCTTTAGTCA[C/T]GGTGTTTCGTTGCAG | 17974 |
rs47166258 | snp | A/G | | | intron-variant | Nck2 | GRCm38.p3 | 1:43481384 | TGTCCTTAATCCCTT[A/G]GCCACCACCCCCTTC | 17974 |
rs47185760 | snp | G/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43449955 | GAATAGCATCCTGCC[G/T]TATATGTGCCACATT | 17974 |
rs47239548 | snp | A/G | | | intron-variant | Nck2 | GRCm38.p3 | 1:43447988 | TGTTGGAGCAGACCG[A/G]ATGACCCCTTGAAAA | 17974 |
rs47308099 | snp | C/G | | | intron-variant | Nck2 | GRCm38.p3 | 1:43447331 | GTTTATAGATACAGA[C/G]GTAGAAACCGGACTT | 17974 |
rs47353986 | snp | C/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43450371 | ATAAATGGCATATTC[C/T]ACCCCTTACCTTGTG | 17974 |
rs47438643 | snp | C/T | | | intron-variant | Nck2 | Mm_Celera | 1:43478687 | CATGCCAGTGATGCC[C/T]TGTGAAACTGGGAGG | 17974 |
rs47486095 | snp | C/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43478033 | TTGTAGTTTTGGACA[C/T]GATGATGGAAATTGC | 17974 |
rs47520020 | snp | C/G | | | intron-variant | Nck2 | Mm_Celera | 1:43448307 | GACCGGGAAGCTTCC[C/G]ATAGAGACTTAGGAA | 17974 |
rs47527453 | snp | C/T | | | intron-variant | Nck2 | Mm_Celera | 1:43515452 | TCTAAGCCTGTTTAT[C/T]ATTTCTATAAAGGAA | 17974 |
rs47602544 | snp | A/G | | | intron-variant | Nck2 | GRCm38.p3 | 1:43450808 | AAGTACTTTTTGCTT[A/G]TTCATGTTTAGTGTT | 17974 |
rs47660291 | snp | A/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43447858 | CTCTTTGATCCGGGC[A/T]TATTCCTGACCTCTG | 17974 |
rs47738875 | snp | C/T | | | intron-variant | Nck2 | Mm_Celera | 1:43483918 | GTTGTTTCAGCTGGT[C/T]TTCTGTAGAAGTAGG | 17974 |
rs47770682 | snp | C/T | | | intron-variant | Nck2 | Mm_Celera | 1:43462568 | TAGCTAAGACTTGAA[C/T]TTGAAGTTTGCCTGC | 17974 |
rs47804476 | snp | C/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43477863 | TCAACTAGGATGTGG[C/T]CACCAGACATGGACT | 17974 |
rs47884920 | snp | A/G | | | intron-variant | Nck2 | Mm_Celera | 1:43536283 | TACCATGGAAGTCCC[A/G]GGGATTGAACTCATC | 17974 |
rs48001654 | snp | A/G/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43449074 | ATTTCACCATCTTCC[A/G/T]TCTCAACTAAGAGGC | 17974 |
rs48006048 | snp | C/T | | | intron-variant | Nck2 | Mm_Celera | 1:43528940 | GATTAGCAAGGATGA[C/T]TGTAGCTGTCCAGAG | 17974 |
rs48084531 | snp | G/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43450489 | GAGTATTATTTCCTT[G/T]AAGTGTGACAAATGC | 17974 |
rs48148353 | snp | A/G | | | intron-variant | Nck2 | Mm_Celera | 1:43450580 | CCAGGAGTTCCAGTC[A/G]AGGGTGACACATATG | 17974 |
rs48208272 | snp | C/T | | | intron-variant | Nck2 | Mm_Celera | 1:43528914 | ATTCTTTCTCTGATT[C/T]TCTTGCCTCAGATTA | 17974 |
rs48298376 | snp | A/G | | | intron-variant | Nck2 | GRCm38.p3 | 1:43447758 | AAAAGGTGGTTTCCA[A/G]CTCCTTGTAGGCTCT | 17974 |
rs48379750 | snp | A/G | | | intron-variant | Nck2 | GRCm38.p3 | 1:43478220 | TCCAAGGTGGTGGGC[A/G]GGGTTTCTTTAAGGT | 17974 |
rs48450264 | snp | C/T | | | intron-variant | Nck2 | Mm_Celera | 1:43447237 | AGTTAGCAACTGTGG[C/T]TTTTCTAGTCTAAAG | 17974 |
rs48510996 | snp | C/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43478657 | TTTGTGGAGAAAACA[C/T]CATGCTAGTGATAGC | 17974 |
rs48536044 | snp | A/G | | | intron-variant | Nck2 | GRCm38.p3 | 1:43490682 | AATAGATTCCCAAAG[A/G]AAACTTAGTGTTCTC | 17974 |
rs48569183 | snp | C/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43481624 | TTGTCAACCCCTCAG[C/T]TTCTTGGAGTTGAGC | 17974 |
rs48751469 | snp | A/G | | | intron-variant | Nck2 | GRCm38.p3 | 1:43448105 | CTTGGTTGCTTTGTA[A/G]GGCACACATGCTTCT | 17974 |
rs48803995 | snp | C/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43478288 | ATAAAGTCACTGTAC[C/T]TGCTATGGTCTGCCT | 17974 |
rs48821793 | snp | A/G | | | intron-variant | Nck2 | Mm_Celera | 1:43483355 | GGGTAAACAATGGTG[A/G]CTTTTATTCAGTTTG | 17974 |
rs48990442 | snp | G/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43449895 | AAGATCTGTAATCTG[G/T]AAATCTGGTctgcaa | 17974 |
rs49024041 | snp | A/C | | | intron-variant | Nck2 | GRCm38.p3 | 1:43457143 | AAAAAAAAGGACCCT[A/C]GCAATGTGGAGGAGG | 17974 |
rs49045463 | snp | C/T | | | intron-variant | Nck2 | Mm_Celera | 1:43450067 | TAGGATGTGTGAGTC[C/T]TTTGGGCATGTGCCA | 17974 |
rs49120461 | snp | A/C | | | intron-variant | Nck2 | GRCm38.p3 | 1:43450267 | AGTTGTTTACATTTA[A/C]ATTTCACTGATATTT | 17974 |
rs49156760 | snp | A/G | | | intron-variant | Nck2 | GRCm38.p3 | 1:43450591 | AGTCAAGGGTGACAC[A/G]TATGTGCGGCACATA | 17974 |
rs49171833 | snp | A/G | | | intron-variant | Nck2 | GRCm38.p3 | 1:43449746 | TGTCAGCCTGTTGTG[A/G]TAGCTCTGGCCAAAG | 17974 |
rs49174443 | snp | C/T | | | intron-variant | Nck2 | Mm_Celera | 1:43483313 | AGTTCCCACAGTGGG[C/T]ACAGTAGCTGGTGGG | 17974 |
rs49252565 | snp | A/G | | | intron-variant | Nck2 | GRCm38.p3 | 1:43483106 | GGGGCAGCTATTTCC[A/G]TCGTGGGATTGAATT | 17974 |
rs49327073 | snp | G/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43477885 | ACATGGACTTGTCTT[G/T]TGCTTTTAACCTCCA | 17974 |
rs49431169 | snp | C/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43449135 | CTTTCTTGGTGGTTT[C/T]CTTTGGACATCTGTG | 17974 |
rs49457602 | snp | A/G | | | intron-variant | Nck2 | Mm_Celera | 1:43505299 | AGTGTGGTAGGCCCA[A/G]CAGCATTGGAGAGGG | 17974 |
rs49535106 | snp | A/G | | | intron-variant | Nck2 | GRCm38.p3 | 1:43449952 | GCTGAATAGCATCCT[A/G]CCGTATATGTGCCAC | 17974 |
rs49547668 | snp | C/T | | | intron-variant | Nck2 | Mm_Celera | 1:43483505 | TAAATCAGATCCTCA[C/T]GGTTTATTTTTTTAT | 17974 |
rs49622057 | snp | A/G | | | intron-variant | Nck2 | Mm_Celera | 1:43483530 | TTTTATTTTTGATGA[A/G]GGAAACAGCAGGGTA | 17974 |
rs49695150 | snp | A/G | | | intron-variant | Nck2 | Mm_Celera | 1:43483550 | ACAGCAGGGTAGGCA[A/G]CTCCAGCTTATCCAT | 17974 |
rs49741114 | snp | C/G | | | intron-variant | Nck2 | GRCm38.p3 | 1:43449115 | TCCTGGGACATCCAA[C/G]AGATCTTTCTTGGTG | 17974 |
rs49797700 | snp | A/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43477450 | CTGGGATTAAAGGTG[A/T]GTGCCACCATGCCTG | 17974 |
rs49805729 | snp | C/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43462863 | CTGAGGGAGGCCTGG[C/T]CTGAGGGTGTCGGCT | 17974 |
rs49813815 | snp | C/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43449891 | GTTGAAGATCTGTAA[C/T]CTGGAAATCTGGTCT | 17974 |
rs49845274 | snp | C/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43449173 | TCCTAGTTGTCTTCA[C/T]TATTTCTTACCCTGG | 17974 |
rs49879953 | snp | A/G | | | intron-variant | Nck2 | GRCm38.p3 | 1:43448327 | AGACTTAGGAAATTC[A/G]TTTTCCCATCCAGAG | 17974 |
rs49947225 | snp | C/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43462196 | TAAAATGACTAAATA[C/T]AAATTCAACAATGTT | 17974 |
rs49988917 | snp | C/T | | | intron-variant | Nck2 | Mm_Celera | 1:43503911 | TCCTAGTGTAACCTG[C/T]GGATATTCTGCTTTG | 17974 |
rs50033642 | snp | G/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43450193 | CCTCTCTCTGCAGCC[G/T]CACCAGCATTTGTTT | 17974 |
rs50143225 | snp | C/G | | | intron-variant | Nck2 | Mm_Celera | 1:43503956 | GATGGCAAAGCGAAG[C/G]GGTCATTTAATTCAT | 17974 |
rs50159332 | snp | A/C | | | intron-variant | Nck2 | Mm_Celera | 1:43483545 | AGGAAACAGCAGGGT[A/C]GGCAGCTCCAGCTTA | 17974 |
rs50201156 | snp | G/T | | | intron-variant | Nck2 | Mm_Celera | 1:43483366 | GGTGACTTTTATTCA[G/T]TTTGTTCCTTTGAAA | 17974 |
rs50209130 | snp | G/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43447332 | TTTATAGATACAGAG[G/T]TAGAAACCGGACTTT | 17974 |
rs50217988 | snp | A/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43449741 | GCCCATGTCAGCCTG[A/T]TGTGATAGCTCTGGC | 17974 |
rs50301724 | snp | C/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43449223 | ATCATAGCATTTGAT[C/T]CATAGTTCATGTGTG | 17974 |
rs50381227 | snp | A/C | | | intron-variant | Nck2 | Mm_Celera | 1:43457415 | TGGGGGACAGAGGAA[A/C]TGCTGAAGTTAGGTG | 17974 |
rs50457530 | snp | A/G | | | intron-variant | Nck2 | GRCm38.p3 | 1:43450408 | TGTCCAAATTCAAGT[A/G]GACTAGAAATACTGA | 17974 |
rs50607231 | snp | C/T | | | intron-variant | Nck2 | Mm_Celera | 1:43515657 | TTGTCTTACTGTTCT[C/T]GATAACACTTTGAGT | 17974 |
rs50623931 | snp | C/G | | | intron-variant | Nck2 | Mm_Celera | 1:43515750 | GCTTCAAGTATGTCT[C/G]CATTTAATTTGGCTG | 17974 |
rs50641257 | snp | A/G | | | intron-variant | Nck2 | GRCm38.p3 | 1:43450878 | AAAATGCCAGGGGTC[A/G]TGAGCTTAGGTTGAA | 17974 |
rs50757092 | snp | A/G | | | intron-variant | Nck2 | GRCm38.p3 | 1:43447735 | CCTTTAAAATGGGTC[A/G]AACTTATAAAAGGTG | 17974 |
rs50796039 | snp | A/G | | | intron-variant | Nck2 | GRCm38.p3 | 1:43456083 | TGCTATCAGATTTGG[A/G]TTGGGAAATAGAGAC | 17974 |
rs50807097 | snp | A/G | | | intron-variant | Nck2 | GRCm38.p3 | 1:43450475 | ATTTTTTTTGACTTG[A/G]GTATTATTTCCTTTA | 17974 |
rs50824579 | snp | A/G | | | intron-variant | Nck2 | GRCm38.p3 | 1:43462451 | AAATTACAGGTACAC[A/G]CCACTGTATCTAGCT | 17974 |
rs50935165 | snp | C/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43480845 | TTTTTTTTTTTCTTT[C/T]TTTTTTTCCATTTTC | 17974 |
rs50980004 | snp | A/G | | | intron-variant | Nck2 | GRCm38.p3 | 1:43477729 | TTACAGGGAGATGGT[A/G]TTAGGAGGAGAACCC | 17974 |
rs51011616 | snp | A/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43447876 | TTCCTGACCTCTGTC[A/T]TGAACATTGGGGTAC | 17974 |
rs51173621 | snp | C/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43481746 | CCTGTAGCAGTAACA[C/T]ACAGTGACCCTCAGT | 17974 |
rs51189838 | snp | C/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43448938 | CATAGCAGTACCACG[C/T]TAGGGTCACACTGGT | 17974 |
rs51271235 | snp | A/G | | | intron-variant | Nck2 | GRCm38.p3 | 1:43449093 | CAACTAAGAGGCAAT[A/G]ACTGTGTCCTGGGAC | 17974 |
rs51302579 | snp | C/G | | | intron-variant | Nck2 | Mm_Celera | 1:43515427 | GCCATTGTTGTTTCC[C/G]TAATTTCTTTCTAAG | 17974 |
rs51341124 | snp | G/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43457416 | GGGGGACAGAGGAAC[G/T]GCTGAAGTTAGGTGA | 17974 |
rs51365969 | snp | A/G | | | intron-variant | Nck2 | Mm_Celera | 1:43552915 | TCCCCTAATTGGGCT[A/G]CCTTGTCTGGCCTCA | 17974 |
rs51417232 | snp | A/G | | | intron-variant | Nck2 | GRCm38.p3 | 1:43450440 | ATTACACTCAGGAAT[A/G]TACTATATATGAAAT | 17974 |
rs51419535 | snp | A/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43561883 | ATAAATAAATCTTTT[A/T]AAAAAAAAAAGAAAG | 17974 |
rs51428683 | snp | A/G | | | intron-variant | Nck2 | GRCm38.p3 | 1:43450309 | ACACTTTTTGAGAAA[A/G]CATTCCCAAAATGAA | 17974 |
rs51433615 | snp | A/C | | | intron-variant | Nck2 | Mm_Celera | 1:43536787 | AGGCTTAATCCTCAA[A/C]TATCTTTTATATTAA | 17974 |
rs51494471 | snp | C/T | | | intron-variant | Nck2 | Mm_Celera | 1:43515399 | CAGAACTCCAGTGGC[C/T]CAAGCTCTAAGAGCC | 17974 |
rs51524111 | snp | C/T | | | intron-variant | Nck2 | Mm_Celera | 1:43505001 | CAGGGCAGCCAGAGC[C/T]ACATAGTGAGACTGT | 17974 |
rs51599658 | snp | C/G | | | intron-variant | Nck2 | Mm_Celera | 1:43480008 | TTGGGGTTTGTGCCC[C/G]TCTGCATCCTGTAGG | 17974 |
rs51608587 | snp | A/G | | | intron-variant | Nck2 | GRCm38.p3 | 1:43450819 | GCTTATTCATGTTTA[A/G]TGTTCTGCATAGAAT | 17974 |
rs51631961 | snp | A/G | | | intron-variant | Nck2 | GRCm38.p3 | 1:43457431 | TGCTGAAGTTAGGTG[A/G]GGCTGAGCAATGTAT | 17974 |
rs51872958 | snp | C/T | | | intron-variant | Nck2 | GRCm38.p3 | 1:43461817 | ACAAACCCTTTCCTC[C/T]CAGCTCGTTCTTTAG | 17974 |