SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13459245 | snp | A/G | 0.375 | 0.216506 | missense, upstream-variant-2KB | Nck1 | GRCm38.p3 | 9:100508644 | GAAAGATGGCTGAAG[A/G]AGTGGTGGTGGTGGC | 17973 |
rs29597018 | snp | A/G | 0.48 | 0.0979796 | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100508772 | GAGGCCAGGAATTAT[A/G]ACTCATACCAGCAAA | 17973 |
rs29645256 | snp | A/G/T | 0.444444 | 0.157135 | intron-variant | Nck1 | GRCm38.p3 | 9:100519995 | AAAAAAAGAAAGAAA[A/G/T]AACTACCTTCAAAAA | 17973 |
rs29649401 | snp | C/G | 0.387812 | 0.208586 | intron-variant | Nck1 | Mm_Celera | 9:100533088 | ACACATCCTTTTACA[C/G]AAACAAACAAACCAC | 17973 |
rs29686533 | snp | A/C | 0.46875 | 0.121031 | intron-variant | Nck1 | Mm_Celera | 9:100521523 | ATGCCTGTCTCTTTG[A/C]CTGGCTTGTATTTTA | 17973 |
rs29688436 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nck1 | Mm_Celera | 9:100522454 | TAAGCCACAACATCA[C/T]ATAGTTTATATTGCT | 17973 |
rs29689723 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Nck1 | GRCm38.p3 | 9:100506437 | GCTTTACTTCAAATG[C/T]CTGTGTGTGGTACAA | 17973 |
rs29691374 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Nck1 | GRCm38.p3 | 9:100509231 | TTCTGAACACTTTTG[C/T]CTTCCCATATAAGTT | 17973 |
rs29694935 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Nck1 | Mm_Celera | 9:100500797 | TTTTTTTTTTTTTTT[G/T]TACTGAGTTTTTTGT | 17973 |
rs29696025 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Nck1 | Mm_Celera | 9:100542905 | GATCACATTAGAACA[A/T]AATTTGAGCAACAAT | 17973 |
rs29740236 | snp | A/C | 0.375 | 0.216506 | intron-variant | Nck1 | Mm_Celera | 9:100538245 | GAACCTAGAGTTACA[A/C]AGCTCCATTGCAGAA | 17973 |
rs29745633 | snp | G/T | 0.487535 | 0.077957 | intron-variant | Nck1 | Mm_Celera | 9:100498597 | CAATGTCTTATACTC[G/T]ATTACTTGTCTGCTT | 17973 |
rs29748244 | snp | C/T | 0.473373 | 0.11227 | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100547788 | TAAAGGAAATAAGAA[C/T]CCTCCATATCTTAAG | 17973 |
rs29787950 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nck1 | Mm_Celera | 9:100511194 | TATAAGGTAGAGAGC[C/T]ATTAAAGAAGGCATG | 17973 |
rs29790474 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nck1 | Mm_Celera | 9:100541264 | AATTTCTGCCTCTCC[C/T]AAGGAAATGTTTCCA | 17973 |
rs29791574 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nck1 | Mm_Celera | 9:100496834 | AGACCGAGTTATACA[A/G]TGAGTCATTCTCTCA | 17973 |
rs29793198 | snp | G/T | 0.387812 | 0.208586 | intron-variant | Nck1 | Mm_Celera | 9:100526153 | CGTGTGTGAATGCTT[G/T]TGGTACCATTCAGCT | 17973 |
rs29839551 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nck1 | Mm_Celera | 9:100540397 | ATACATCATGGAAAA[A/G]AGACATGCAGTAAAA | 17973 |
rs29840671 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Nck1 | GRCm38.p3 | 9:100496590 | AGAATTTTTAAAAAA[A/C/T]AACTGTCAAATTTTA | 17973 |
rs29841207 | snp | A/G | 0.455 | 0.143091 | intron-variant | Nck1 | Mm_Celera | 9:100495946 | AAAGTAGTGAACACA[A/G]AAAGTAGTTTTCAGA | 17973 |
rs29921954 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Nck1 | Mm_Celera | 9:100506616 | ACCAGCTTACATAAA[C/T]CCACTGAGTTCTTTC | 17973 |
rs29931030 | snp | A/T | 0.48 | 0.0979796 | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100547821 | CTTTCCCAGTAAGCT[A/T]TTGACAGCTTATATA | 17973 |
rs29932990 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Nck1 | Mm_Celera | 9:100525564 | TTCAGCTCATTCTGC[A/G]GGCAGTGACTACCTG | 17973 |
rs29940234 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Nck1 | Mm_Celera | 9:100545082 | TTTCTCCTTGGACTA[C/T]TTCTCTGTTCATGTT | 17973 |
rs29974548 | snp | A/G | 0.375 | 0.216506 | intron-variant, utr-variant-3-prime | Nck1 | Mm_Celera | 9:100494989 | TGGCTTGTGACAGAT[A/G]CAATATCTGAAAATA | 17973 |
rs29982802 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Nck1 | Mm_Celera | 9:100527074 | TGCTATCCTACATTT[C/T]TTAGAAATGCATAAA | 17973 |
rs30040183 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Nck1 | Mm_Celera | 9:100523422 | CAAACTGTGAAAATG[C/T]ATAACAAAGAATTGC | 17973 |
rs30041229 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nck1 | GRCm38.p3 | 9:100539186 | GAACAGAGGCAGGCC[A/G]ATCCCTGGGATTTCA | 17973 |
rs30086437 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Nck1 | Mm_Celera | 9:100543305 | CATCACAAAACACAC[C/T]GCTCTGTGCGCTAAC | 17973 |
rs30176812 | snp | C/T | 0.5 | 0 | intron-variant | Nck1 | Mm_Celera | 9:100530167 | GCAGATAAATAAAGG[C/T]ACTTGTCACACAAGC | 17973 |
rs30182162 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nck1 | Mm_Celera | 9:100505139 | CAGTGAGTTCTAAGA[C/T]ATCCAGGAACACACT | 17973 |
rs30183511 | snp | C/T | 0.5 | 0 | downstream-variant-500B | Nck1 | Mm_Celera | 9:100494484 | CTCAGCGCAGAACAC[C/T]TGCTTTTCATGTGTA | 17973 |
rs30231492 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Nck1 | Mm_Celera | 9:100540794 | TCTGTTTTGGCTAGG[G/T]TTTTGCTGCTGTTTT | 17973 |
rs30233201 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nck1 | Mm_Celera | 9:100542264 | AACACACACAAAAAA[A/G]GGGAGGATAGGCAAA | 17973 |
rs30276774 | snp | C/G | 0.375 | 0.216506 | intron-variant | Nck1 | Mm_Celera | 9:100538459 | GTTACATATAACAAA[C/G]CCACAGCCAGTATCA | 17973 |
rs30327786 | snp | A/G | 0.5 | 0 | intron-variant, utr-variant-5-prime | Nck1 | Mm_Celera | 9:100545979 | GTGTGTCCGCACGCG[A/G]GCGAGGCCGTCTCAC | 17973 |
rs30334000 | snp | A/T | 0.465374 | 0.126941 | intron-variant | Nck1 | Mm_Celera | 9:100526518 | AGGCAGCAAACTTCT[A/T]AGGTGAACAAACAAG | 17973 |
rs30373936 | snp | C/T | 0.5 | 0 | intron-variant | Nck1 | Mm_Celera | 9:100537065 | ATATCATCATTGCTA[C/T]TATTATTATATTATT | 17973 |
rs30384351 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nck1 | Mm_Celera | 9:100532356 | TTACATAAAATAAAT[C/T]CCAGCATGCATATAT | 17973 |
rs30386257 | snp | A/G/T | 0.387812 | 0.208586 | intron-variant | Nck1 | GRCm38.p3 | 9:100535064 | CTTGGGTTCTGCACT[A/G/T]AGATGACAAAGCAAG | 17973 |
rs30387273 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nck1 | Mm_Celera | 9:100538157 | AAGAACTAGCAAAGA[A/G]CAAAACAAACTCAAC | 17973 |
rs30427730 | snp | A/G | 0.5 | 0 | intron-variant | Nck1 | GRCm38.p3 | 9:100514509 | CTCACACAGACATAT[A/G]TGCAAGTAACACCAA | 17973 |
rs30430419 | snp | C/T | 0.5 | 0 | intron-variant | Nck1 | Mm_Celera | 9:100544601 | CTGGCATTGAAAGCA[C/T]CCATTCTTCCACATT | 17973 |
rs30438113 | snp | G/T | 0.375 | 0.216506 | intron-variant | Nck1 | Mm_Celera | 9:100532450 | CAGATGATGATGATG[G/T]TGGATCCTCGGAATC | 17973 |
rs30438859 | snp | A/T | 0.5 | 0 | intron-variant | Nck1 | Mm_Celera | 9:100510546 | ATTGACTACCATGTC[A/T]GTTTTCTCAACAATG | 17973 |
rs30478816 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Nck1 | Mm_Celera | 9:100520416 | GCTTTCTGTCTCTGT[C/T]TCCCAAGTGCTGGGA | 17973 |
rs30486532 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Nck1 | Mm_Celera | 9:100499034 | TCCTTAATTTCCTTA[C/T]TTCTGGCTAATGAGG | 17973 |
rs30516612 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Nck1 | Mm_Celera | 9:100525987 | ACATCAGAATTGACT[C/T]AGATGTTCACGGGTC | 17973 |
rs33198484 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck1 | Mm_Celera | 9:100502163 | TCACCTAACCATTTA[C/T]GTGATAATTACCAAG | 17973 |
rs33198485 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck1 | Mm_Celera | 9:100502725 | TCTAGCATTTTAGTT[C/T]ACCACAATCATCCTA | 17973 |
rs33198486 | snp | G/T | 0.32 | 0.24 | intron-variant | Nck1 | Mm_Celera | 9:100502752 | CCTACCTTCAATTTG[G/T]TTTTTTTTCCCCAAA | 17973 |
rs33198487 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck1 | Mm_Celera | 9:100502790 | ATTCCATTGCTACTC[C/T]TATTCTGATTGTAAG | 17973 |
rs33198488 | snp | G/T | 0.5 | 0 | intron-variant | Nck1 | Mm_Celera | 9:100502799 | CTACTCTTATTCTGA[G/T]TGTAAGTCTTAAGGG | 17973 |
rs33198489 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck1 | Mm_Celera | 9:100502820 | GTCTTAAGGGGTCTA[C/T]TATGAAAACTTAAAA | 17973 |
rs33198490 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Nck1 | Mm_Celera | 9:100503035 | GATAACAGTTGTCAG[G/T]TTTTTTTTGTTATTT | 17973 |
rs33198491 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Nck1 | Mm_Celera | 9:100503147 | ACACTGAGGAGGGAG[A/T]TAACTCTGAAGCAGT | 17973 |
rs33198492 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100504008 | GATAGTGTTATTCTT[G/T]CTCAGGCAAATCTTT | 17973 |
rs33198493 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Nck1 | Mm_Celera | 9:100504104 | GAAAGCATCAGATAC[A/C]AAGTGAACAAACTGC | 17973 |
rs33198524 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100528797 | AGGAAGTTGTTGTTG[A/G]CCAGTGACAGACCTG | 17973 |
rs33198525 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100531102 | GTAATTTCTTTTTCT[A/C]AGTTTTAATGATATG | 17973 |
rs33198526 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck1 | Mm_Celera | 9:100531420 | TTTGGATTCATAAGA[A/G]AAGCATCTCTTCTCT | 17973 |
rs33198527 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Nck1 | Mm_Celera | 9:100531712 | GATACATTTTAAACT[A/T]TTTAAACTATAAGTT | 17973 |
rs33198528 | snp | C/T | 0.18 | 0.24 | intron-variant | Nck1 | Mm_Celera | 9:100531713 | ATACATTTTAAACTA[C/T]TTAAACTATAAGTTT | 17973 |
rs33198529 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck1 | Mm_Celera | 9:100531938 | CACTGTGTGACCCTG[C/T]GCATCACAGCACCCG | 17973 |
rs33198530 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100532021 | GCTTCTAGCCTAGAT[A/G]AGAAAGCACAAGCCC | 17973 |
rs33198531 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100532708 | TGAAATAATAACAAA[A/G]TGAGCATCTACATCT | 17973 |
rs33198532 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100532820 | TCAGGACTCATGTAA[A/G]TATCTTCTATTAAAC | 17973 |
rs33198533 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100532851 | TCCCAAAGAGTTCCA[A/G]AAAGTATAATAAAAT | 17973 |
rs33199294 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Nck1 | Mm_Celera | 9:100504123 | TGAACAAACTGCCAC[A/G]TTTAGCTGGCCAGAA | 17973 |
rs33199295 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck1 | Mm_Celera | 9:100504218 | ATGGAGTTCTGCACC[A/G]ACACAACCACAGCAG | 17973 |
rs33199296 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100504249 | CTCTTACTAAATTTT[G/T]TTCTTTGTGTCAGCC | 17973 |
rs33199297 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100504359 | ACTAAGTAAATGCTC[A/G]ACAGAATGGGTTCAG | 17973 |
rs33199298 | snp | G/T | 0.32 | 0.24 | intron-variant | Nck1 | Mm_Celera | 9:100504522 | TGTAGAGCTGGAAGG[G/T]ACTTTCCAGGATCAT | 17973 |
rs33199299 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100504851 | ATTTAGAAGTTAGGT[A/G]AATGAAAACCTGTCT | 17973 |
rs33199300 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Nck1 | Mm_Celera | 9:100504901 | AGCAAAATAAACATC[A/G]ATATTATAGGGATTG | 17973 |
rs33199301 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck1 | Mm_Celera | 9:100504982 | ACAGATACAGTTAGG[A/G]CTGAATATGCTTTAT | 17973 |
rs33199302 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck1 | Mm_Celera | 9:100505270 | TCATCTAACTCCCTA[A/G]CAGATTCTGCAAGAG | 17973 |
rs33199303 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100505486 | TGCTGAACAATCTTG[C/T]CAAACCATCGAGCTG | 17973 |
rs33199474 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100533168 | TTAAAGGAATATATG[C/T]ACACAAGCCAGGGCA | 17973 |
rs33199475 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100533226 | ATACACTTGTATTTA[C/G]TTCATATCCATCAAG | 17973 |
rs33199476 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100533296 | CTACCTATTCTGATG[A/G]CTAGTACTGTATACT | 17973 |
rs33199477 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nck1 | Mm_Celera | 9:100533299 | CCTATTCTGATGGCT[A/G]GTACTGTATACTACT | 17973 |
rs33199478 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100533330 | AGCTCTTCCCATTGA[A/G]TGCACTTCTCTGACC | 17973 |
rs33199479 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Nck1 | Mm_Celera | 9:100533367 | TCTACAACTTTAGCT[A/C]TCTCAGTAGACACAA | 17973 |
rs33199480 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100533375 | TTTAGCTATCTCAGT[A/G]GACACAACTACAGAC | 17973 |
rs33199481 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Nck1 | Mm_Celera | 9:100533524 | AACAAGCTTCGTGAT[A/G]CGAGGGTAGGGTCAG | 17973 |
rs33199482 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck1 | Mm_Celera | 9:100533740 | TCTTATAGATGTTGG[A/G]GAAAATACAAGGATG | 17973 |
rs33199483 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100533878 | CTCTAAACTCAACAT[A/T]TAAGAGTCCAGCAAG | 17973 |
rs33200064 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Nck1 | Mm_Celera | 9:100505904 | CTCAAAGATCTAAAA[A/C]TGTATTTGTTCTCTA | 17973 |
rs33200065 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck1 | Mm_Celera | 9:100506065 | CTCTTGGACTCTCAT[C/T]AGATCACTGTTTCCT | 17973 |
rs33200066 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck1 | Mm_Celera | 9:100506089 | GTTTCCTTAGGCTTT[C/T]TGACTCTTAAGAGAC | 17973 |
rs33200067 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck1 | Mm_Celera | 9:100506243 | TTTACTTGTAAGTCA[A/G]TACTTGTAGTTTACT | 17973 |
rs33200068 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck1 | Mm_Celera | 9:100506262 | TTGTAGTTTACTAGA[A/G]CTCTTATTAAATGTT | 17973 |
rs33200069 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck1 | Mm_Celera | 9:100506292 | TATCTTGACATTATT[C/T]CAACAAAGCTTAAGT | 17973 |
rs33200070 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck1 | Mm_Celera | 9:100506564 | GCAGTGAAAATATCA[C/T]CGCCATTTACCTTCT | 17973 |
rs33200071 | snp | A/G | 0.142012 | 0.225474 | intron-variant, utr-variant-5-prime | Nck1 | Mm_Celera | 9:100506992 | CAAGTAACTCAGGGC[A/G]GCAGCAAAAACAGGA | 17973 |
rs33200072 | snp | A/T | 0.244898 | 0.249948 | intron-variant, utr-variant-5-prime | Nck1 | Mm_Celera | 9:100507036 | CATTGTAACAGAAAA[A/T]ATTAAAGCTAGTATG | 17973 |
rs33200073 | snp | G/T | 0.277778 | 0.248452 | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100507522 | AAGAAACATTTACCT[G/T]ATATTGCCAATAATT | 17973 |
rs33200174 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100534356 | GCTGTAAGAACCACT[C/T]TGTGTCAGCTCCTGA | 17973 |
rs33200175 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100534405 | CTGCTGTCCTTGCAG[A/G]TCCTCTATAGTCTGT | 17973 |
rs33200176 | snp | C/G | 0.444444 | 0.157135 | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100546973 | GCCTAGCACATCATC[C/G]TCAACAATCGAGGAA | 17973 |
rs33200177 | snp | A/G | 0.35503 | 0.226867 | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100547242 | TTTAGCTATACTACA[A/G]GCCCTACCTGTAAAT | 17973 |
rs33200178 | snp | C/G | 0.142012 | 0.225474 | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100547373 | CCTGAGTTTAGTTGA[C/G]AAAAGTAGAACATAA | 17973 |
rs33200179 | snp | A/G | 0.345679 | 0.230967 | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100547818 | GACCTTTCCCAGTAA[A/G]CTATTGACAGCTTAT | 17973 |
rs33200180 | snp | C/T | 0.152778 | 0.230321 | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100547907 | AATCCTACCTATCTG[C/T]TATCAAGAAGTTATC | 17973 |
rs33200181 | snp | A/G | 0.152778 | 0.230321 | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100547992 | TTCTGGATTTAGTAT[A/G]GTTATGCTGTTATAG | 17973 |
rs33200182 | snp | A/G | 0.142012 | 0.225474 | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100548037 | TGTATGGAAGGTGCT[A/G]AAATAGGCACTGCAG | 17973 |
rs33200954 | snp | C/T | 0.260355 | 0.249785 | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100507645 | CCACAAAAAAACTGT[C/T]TCCCTCTTTTTTTAC | 17973 |
rs33200955 | snp | C/T | 0.35503 | 0.226867 | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100507691 | TATTAAGCAATTACA[C/T]GTCTGTCTCCTTGAA | 17973 |
rs33200956 | snp | A/T | 0.260355 | 0.249785 | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100507956 | TCCTATAGATGCGAA[A/T]ATACAGCAATAACCC | 17973 |
rs33200957 | snp | A/G | 0.260355 | 0.249785 | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100508037 | TAAGTGAGATTCATT[A/G]GCGTGTCAAAAAGGT | 17973 |
rs33200958 | snp | A/C | 0.35503 | 0.226867 | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100508049 | ATTAGCGTGTCAAAA[A/C]GGTTCAATAATGTGC | 17973 |
rs33200959 | snp | C/T | 0.142012 | 0.225474 | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100508425 | TCAATAAGAAACAAC[C/T]TACCTAAGGTGTCCT | 17973 |
rs33200960 | snp | C/T | 0.277778 | 0.248452 | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100508742 | TTGTCCAAAAAGACA[C/T]GCTTAAACATTTAAG | 17973 |
rs33200961 | snp | A/C | 0.297521 | 0.245442 | intron-variant | Nck1 | Mm_Celera | 9:100509507 | GCCGTAAGCTCAGCG[A/C]CTGGAGGCTGAGGCA | 17973 |
rs33200962 | snp | A/T | 0.297521 | 0.245442 | intron-variant | Nck1 | Mm_Celera | 9:100510406 | ATATATATATATATA[A/T]GCAAACACTGTCCTG | 17973 |
rs33200963 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Nck1 | Mm_Celera | 9:100510548 | TGACTACCATGTCAG[C/T]TTTCTCAACAATGAA | 17973 |
rs33201794 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Nck1 | Mm_Celera | 9:100510658 | GCCTCAAAATCTGCC[A/G]CACATTGTTTTATGC | 17973 |
rs33201795 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Nck1 | Mm_Celera | 9:100510924 | GTCTGAAATTACTTA[A/C]GCACAAAGAATCTAA | 17973 |
rs33201796 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Nck1 | Mm_Celera | 9:100510957 | TATTACTGACATATG[A/T]TGTGATTTAAGTTAG | 17973 |
rs33201797 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck1 | Mm_Celera | 9:100511546 | TGTCTCCTGTTTGGA[A/G]CATACTTGGATTATC | 17973 |
rs33201798 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nck1 | Mm_Celera | 9:100511596 | TTATTTTTAGCAATA[C/T]AACTTGGGAGACTAA | 17973 |
rs33201799 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck1 | Mm_Celera | 9:100511685 | TGAACTTTTAAGGCC[A/G]ATTAAATGAAAGGAA | 17973 |
rs33201800 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Nck1 | Mm_Celera | 9:100511706 | ATGAAAGGAAAAGAG[A/C]CTTCAGAGAAAAGGT | 17973 |
rs33201801 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nck1 | Mm_Celera | 9:100511767 | TTTCAGGATGAGACC[A/G]GAACTATTTTATCAG | 17973 |
rs33201802 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nck1 | Mm_Celera | 9:100512020 | TTATCATAATGTGCT[C/T]AAAAATGCTAAAGTA | 17973 |
rs33201803 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Nck1 | Mm_Celera | 9:100512127 | GTCTTTATTCCCAGT[A/G]TACAAGTAAGTTTTA | 17973 |
rs33202370 | snp | A/G | 0.244898 | 0.249948 | downstream-variant-500B | Nck1 | Mm_Celera | 9:100494527 | ATATTCAATAGTGTC[A/G]AAAAATGTTGTTGTT | 17973 |
rs33202371 | snp | C/T | 0.444444 | 0.157135 | downstream-variant-500B | Nck1 | Mm_Celera | 9:100494682 | TTCCCCAAACTTGAC[C/T]ATGGCTTATTTCACA | 17973 |
rs33202372 | snp | C/T | 0.231111 | 0.249285 | downstream-variant-500B | Nck1 | Mm_Celera | 9:100494781 | TCAAGAGCCAACTGC[C/T]CAAACTGCTCTCTTC | 17973 |
rs33202373 | snp | C/G | 0.231111 | 0.249285 | downstream-variant-500B | Nck1 | Mm_Celera | 9:100494908 | AACCTATTATCTGGT[C/G]TCTTTTGGATACAAT | 17973 |
rs33202654 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nck1 | Mm_Celera | 9:100512181 | GAGTACTTCAAATTA[C/T]TGGTGATCTAAACAT | 17973 |
rs33202655 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Nck1 | Mm_Celera | 9:100512186 | CTTCAAATTACTGGT[G/T]ATCTAAACATTTAAG | 17973 |
rs33202656 | snp | G/T | 0.375 | 0.216506 | intron-variant | Nck1 | Mm_Celera | 9:100512198 | GGTGATCTAAACATT[G/T]AAGTGATTTGTCTAT | 17973 |
rs33202657 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nck1 | Mm_Celera | 9:100512399 | CTTTCAGTAAGCAGA[C/T]TTAATTCATGGGAAC | 17973 |
rs33202658 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nck1 | Mm_Celera | 9:100512453 | TTATACTCTTCATTA[A/G]CAGAAATGAGCAGGC | 17973 |
rs33202659 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Nck1 | Mm_Celera | 9:100512532 | AAACTAGAAGGGTTT[C/T]ATATGAGGAGTAGCA | 17973 |
rs33202660 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Nck1 | Mm_Celera | 9:100512700 | GTGAAATTCCTAGAT[A/T]CTGTGTCAGGAGAGT | 17973 |
rs33202661 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nck1 | Mm_Celera | 9:100512749 | AAAAATAGCAGAGAG[A/G]CTGGAAACCCCTCTC | 17973 |
rs33202662 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck1 | Mm_Celera | 9:100513111 | TAGCAGAAAGTATGT[A/G]GCAAAGTAATTTATC | 17973 |
rs33202663 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Nck1 | Mm_Celera | 9:100513247 | CCTTGGAAGAGACTA[A/T]TGGAGTTCTAATGTG | 17973 |
rs33203294 | snp | C/G | 0.231111 | 0.249285 | utr-variant-3-prime | Nck1 | Mm_Celera | 9:100495438 | CTCCAGTTACATGAC[C/G]AGTTAAAGCTGTGGA | 17973 |
rs33203295 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nck1 | Mm_Celera | 9:100495919 | CTCCTAACAGTTATC[C/T]ACAGTACCCACAAAG | 17973 |
rs33203296 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Nck1 | Mm_Celera | 9:100496056 | TAATACTCTGTATTT[C/T]CAAAAATAATGGACA | 17973 |
rs33203297 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Nck1 | Mm_Celera | 9:100496323 | AGTCACGAATAGTGA[C/T]TTTTAAATGGTATGC | 17973 |
rs33203298 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck1 | Mm_Celera | 9:100496514 | TCTGTACAATGTATT[C/T]ACAAAAAACCAGTAC | 17973 |
rs33203299 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Nck1 | Mm_Celera | 9:100496671 | TTGTATGGCTTTACT[C/G]TCTAGCTGGTACTGC | 17973 |
rs33203300 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nck1 | Mm_Celera | 9:100496714 | CTTTTATTGCAAATA[C/T]ATTTTAAATGGTGTT | 17973 |
rs33203301 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nck1 | Mm_Celera | 9:100497078 | CAAATTTAATACAAC[C/T]GAAGAAAGTCTCTTA | 17973 |
rs33203302 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck1 | Mm_Celera | 9:100497184 | TGGCTTAAGGAAGCC[A/G]GCCACTCAACCTTTC | 17973 |
rs33203303 | snp | A/C | 0.244898 | 0.249948 | synonymous-codon | Nck1 | GRCm38.p3 | 9:100497411 | ATCACATTGTGGAGG[A/C]GATGGTTCCAAACCT | 17973 |
rs33203514 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck1 | Mm_Celera | 9:100513357 | CCTTATGTTCCTCTG[A/G]CACACACTCCTAACC | 17973 |
rs33203515 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Nck1 | Mm_Celera | 9:100513465 | CTTCTAAAACAAAGA[G/T]TTAAATAAACATCTT | 17973 |
rs33203516 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100514571 | AAAAGGAGAAAATGG[A/G]GACAAGAGAATTGTG | 17973 |
rs33203517 | snp | G/T | 0.32 | 0.24 | intron-variant | Nck1 | Mm_Celera | 9:100514657 | AACAAAAAACTGAGA[G/T]AACTTATGTTGAGCT | 17973 |
rs33203518 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck1 | Mm_Celera | 9:100514687 | TCAAACATCTTGGCT[C/T]ACAATTTTGAGTTAG | 17973 |
rs33203519 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100514707 | TTTTGAGTTAGCCCA[C/T]AATTAGCTAGTATTG | 17973 |
rs33203520 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Nck1 | Mm_Celera | 9:100514768 | ATGGTTAAGAAGCAA[A/C]AGAGAAAGGAAGGGA | 17973 |
rs33203521 | snp | A/T | 0.297521 | 0.245442 | intron-variant | Nck1 | Mm_Celera | 9:100516561 | TTATAATCATGTATG[A/T]GTGTGTATATATATG | 17973 |
rs33203522 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Nck1 | Mm_Celera | 9:100520728 | AGGAAAATTCACGTG[A/C]AAGGAGTTCTTAAAC | 17973 |
rs33203523 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck1 | Mm_Celera | 9:100523402 | ACAATCATACAATTA[C/T]AATACAAACTGTGAA | 17973 |
rs33204174 | snp | C/T | 0.244898 | 0.249948 | synonymous-codon | Nck1 | GRCm38.p3 | 9:100497831 | CAATGACAACTCATC[C/T]TCTCTCTCAGCCATG | 17973 |
rs33204175 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck1 | Mm_Celera | 9:100498084 | GATCATCTTTTGGGA[A/G]ATGAAATACAAGTTG | 17973 |
rs33204176 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck1 | Mm_Celera | 9:100498153 | CTTCTTTTCTCCTGC[C/T]AAAGCCAAGAAATAA | 17973 |
rs33204177 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nck1 | Mm_Celera | 9:100498204 | CATGTTGAATTTTCT[C/T]GTGTTAAAATGGTTT | 17973 |
rs33204178 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Nck1 | Mm_Celera | 9:100498350 | AAATTAGTACCTGTG[C/T]ACATATAAAATTATA | 17973 |
rs33204179 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Nck1 | Mm_Celera | 9:100498578 | CCTGTGAGCCTTGCT[C/G]TAACAATGTCTTATA | 17973 |
rs33204180 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck1 | Mm_Celera | 9:100498618 | TTGTCTGCTTCCTAA[C/T]AGAAGAGTCAGCTTC | 17973 |
rs33204181 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck1 | Mm_Celera | 9:100499207 | AAAGCGAAGTGGCAG[A/G]GCAAGGCTCAGTGAA | 17973 |
rs33204182 | snp | A/C | 0.32 | 0.24 | intron-variant | Nck1 | Mm_Celera | 9:100499799 | CTCAAAGATAAAGAA[A/C]TTAAGACATTCTTAA | 17973 |
rs33204183 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck1 | Mm_Celera | 9:100499845 | CTTGTGCTTTTTAAG[A/G]AAATGTAAAAAATAG | 17973 |
rs33204494 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100523496 | AATCCTTAGGTTACT[G/T]GATGGCTAAGAAACA | 17973 |
rs33204495 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100523533 | AATCACAATTGACTA[C/T]ATCCATTTTAAAGTG | 17973 |
rs33204496 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100523831 | ATTTCACATGTAAAG[C/G]TGGAGACAATCCTCA | 17973 |
rs33204497 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck1 | Mm_Celera | 9:100524056 | AAGTTAACATACAGA[A/G]GAGGAGGCTCTCAAG | 17973 |
rs33204498 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Nck1 | Mm_Celera | 9:100524879 | TTAAAATCCTAGCAC[A/G]TTTCACAGCACTACT | 17973 |
rs33204499 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nck1 | GRCm38.p3 | 9:100524966 | TAAACCCAGTTAACT[A/G]TATGACCAAGCCAAT | 17973 |
rs33204500 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nck1 | Mm_Celera | 9:100525052 | ATCCTTTTAACAGGA[C/T]TCAAGTGAATGTACA | 17973 |
rs33204501 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100525152 | GGTCTCCTGTTCCCA[A/G]TCTCACTTTCTTCTA | 17973 |
rs33204502 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nck1 | Mm_Celera | 9:100525214 | AAGTTAGCTGGAAAC[A/G]TGAATTTTTCCTTTA | 17973 |
rs33204503 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100525277 | AATGAAGTTTCAAAT[A/G]AATTTGCCTTGAGTT | 17973 |
rs33205104 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Nck1 | Mm_Celera | 9:100499866 | TAAAAAATAGTCTTC[A/T]AGATGGAAATAAAAA | 17973 |
rs33205105 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Nck1 | GRCm38.p3 | 9:100500468 | TTATACCATCCAAAC[A/C]ACATTGGGAATGACT | 17973 |
rs33205106 | snp | A/T | 0.32 | 0.24 | intron-variant | Nck1 | Mm_Celera | 9:100500478 | CAAACCACATTGGGA[A/T]TGACTTAAACTTGTT | 17973 |
rs33205107 | snp | A/G | 0.32 | 0.24 | intron-variant | Nck1 | Mm_Celera | 9:100501118 | CAACTAATATCTCAA[A/G]TGAGAACACATTAAA | 17973 |
rs33205108 | snp | A/C | 0.32 | 0.24 | intron-variant | Nck1 | Mm_Celera | 9:100501181 | TTTAAAGGAAGAAAT[A/C]TAAGGGCATGGTACA | 17973 |
rs33205109 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck1 | Mm_Celera | 9:100501446 | TTTTTTATTTTCACC[C/T]TAATGCTAAATACAG | 17973 |
rs33205110 | snp | C/T | 0.32 | 0.24 | intron-variant | Nck1 | Mm_Celera | 9:100501504 | CTATCCCCAGTGCCT[C/T]GCCTATATTAAATGT | 17973 |
rs33205111 | snp | A/C/T | 0.48 | 0.0979796 | intron-variant | Nck1 | GRCm38.p3 | 9:100501632 | ATGATGGAATGGAGA[A/C/T]CCGGCATGATGGAAT | 17973 |
rs33205112 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nck1 | GRCm38.p3 | 9:100501692 | GGCATGATGGAATGG[A/G]GATCCGGCATGATGG | 17973 |
rs33205113 | snp | C/T | 0.5 | 0 | intron-variant | Nck1 | GRCm38.p3 | 9:100501737 | ATGATGGAATGGGGA[C/T]CCGGCATGATGGAAT | 17973 |
rs33205464 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100525805 | AAAGGTAAAAGCAGA[C/T]GTGACATGGGATCTG | 17973 |
rs33205465 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck1 | Mm_Celera | 9:100525829 | GGATCTGTGTGATAT[A/G]ATCAAGAGAACTAAC | 17973 |
rs33205466 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100525929 | GTCATTTGAGTCCAA[A/G]TATCTGGATGGTATT | 17973 |
rs33205467 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100526083 | ATTGCTGAGCAAAAA[C/G]TGTCCACTTCACCAA | 17973 |
rs33205468 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100526339 | TACTGTATGGGGCTA[C/T]GGCTTCAGAAGAGCA | 17973 |
rs33205469 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Nck1 | Mm_Celera | 9:100526430 | CAGCTTATAGATGCT[A/T]AATGGCTCAGCATCT | 17973 |
rs33205470 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nck1 | Mm_Celera | 9:100527022 | TTACAGCTACTGCTA[C/T]CATTCATTAATATCT | 17973 |
rs33205471 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nck1 | Mm_Celera | 9:100527201 | CATTTCCATTTTCAA[A/G]TCAACATCAGAAGCC | 17973 |
rs33205472 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100527381 | TGTTGGACTCAGTAA[C/T]GAATCATAACCTAAT | 17973 |
rs33205824 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nck1 | Mm_Celera | 9:100501892 | ATGGGGAACAAGCAT[C/T]CATAAGTTGTTTTCT | 17973 |
rs33205825 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nck1 | Mm_Celera | 9:100501914 | TTGTTTTCTAACCTA[C/T]TTATCTGTGCTGCGG | 17973 |
rs33205826 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Nck1 | Mm_Celera | 9:100501993 | ACACAATAAATAACT[A/G]TAATACATTTTTCTA | 17973 |
rs33205827 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Nck1 | Mm_Celera | 9:100502065 | ACAACTTTGTTTCTA[G/T]TACCAGAAAATGGAC | 17973 |
rs33670594 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nck1 | Mm_Celera | 9:100539375 | TAGGAAAAAAAATCA[A/G]TAAGACCACATACTA | 17973 |
rs33674602 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nck1 | Mm_Celera | 9:100541833 | AAGAAATCACCCTGC[C/T]TCTCTGCCTCCCAGG | 17973 |
rs33684527 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Nck1 | Mm_Celera | 9:100522192 | GGAAGGGGGGGGGGG[A/C]GCATCTACAGGGAAA | 17973 |
rs33704250 | snp | C/T | 0.5 | 0 | intron-variant | Nck1 | Mm_Celera | 9:100496101 | TAAATTTCCCCCCCA[C/T]CCCCAAGACAGGGTT | 17973 |
rs33736384 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nck1 | Mm_Celera | 9:100539656 | GCTATACAGAGAAAC[C/T]CTGTCTCAAAAAAAA | 17973 |
rs33741345 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nck1 | Mm_Celera | 9:100538492 | CTGGGAAAAGCTAGA[A/G]TGACTTCTGTGATCA | 17973 |
rs33775228 | snp | A/G | 0.48 | 0.0979796 | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100546135 | GGGGCGCGCGCAACC[A/G]GTGGGCGGACCGTTG | 17973 |
rs46104071 | snp | C/T | | | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100547180 | GGAATCAAACTCAGG[C/T]CCCTTGGAAGACCAG | 17973 |
rs46447584 | snp | A/G/T | | | intron-variant | Nck1 | GRCm38.p3 | 9:100501609 | CTAATGACCCTGTTT[A/G/T]ACCCGGCATGATGGA | 17973 |
rs46555742 | snp | C/T | | | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100546978 | GCACATCATCCTCAA[C/T]AATCGAGGAATTAAT | 17973 |
rs46757754 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100524746 | CACCTCTGGTTTTCG[A/C]AAGCACCAGCATCGA | 17973 |
rs47247172 | snp | C/G | | | intron-variant | Nck1 | Mm_Celera | 9:100536432 | ACCCCACCCCCAAAG[C/G]TCCCAGGGACTAAAC | 17973 |
rs47445388 | snp | A/G | | | intron-variant | Nck1 | GRCm38.p3 | 9:100501671 | GGCATGATGGAATGG[A/G]GATCCGGCATGATGG | 17973 |
rs47459294 | snp | C/T | | | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100547220 | TCACTGAATCTCAGC[C/T]CCTTCCTTTAGCTAT | 17973 |
rs47909048 | snp | A/G | | | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100547161 | AACCACCCTGTGGGT[A/G]CTGGGAATCAAACTC | 17973 |
rs48124352 | snp | A/G | | | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100546491 | TGCCTGCATCTGAAA[A/G]GGCCGACCAGCTGCA | 17973 |
rs48503702 | snp | A/G | | | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100547179 | GGGAATCAAACTCAG[A/G]CCCCTTGGAAGACCA | 17973 |
rs48540491 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100533598 | CTCTAAGGAAGGAAC[C/T]GAGGTCATCAGGCTT | 17973 |
rs48545940 | snp | C/T | | | intron-variant | Nck1 | GRCm38.p3 | 9:100501674 | ATGATGGAATGGAGA[C/T]CCGGCATGATGGAAT | 17973 |
rs48913893 | snp | C/G | | | intron-variant | Nck1 | Mm_Celera | 9:100542187 | ATGTTTTGTGAATCT[C/G]AGGCCAGCCTGGTCT | 17973 |
rs49019483 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100504644 | TATCTGAGAGTAGAA[C/T]TAATTTATTATAAAT | 17973 |
rs49060538 | snp | C/T | | | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100547031 | AAATTCATTTTTATT[C/T]TTTGTGTGTTCGAGT | 17973 |
rs49247380 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100538511 | CTTCTGTGATCAGGA[A/G]CAAAGTGGGCTGTCT | 17973 |
rs49758141 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100505218 | CACTCATGACCACAC[C/T]TAGATAGAAACCCAC | 17973 |
rs50388127 | snp | A/G | | | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100547397 | AACATAAAACTGGGG[A/G]AAGGATACTCTGCCT | 17973 |
rs50724102 | snp | A/T | | | upstream-variant-2KB | Nck1 | GRCm38.p3 | 9:100547018 | TTTCATCTTTTAAAA[A/T]TTCATTTTTATTCTT | 17973 |
rs50895596 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100541196 | ATTAGTTGATATAAA[A/T]ATAAAAAGCAAGATT | 17973 |
rs51406610 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100514888 | CTTCCCAACAGCACC[A/G]AGGGCTGGGAAGCAA | 17973 |
rs51649153 | snp | A/G | | | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100546504 | AAGGGCCGACCAGCT[A/G]CAGATCTTAGGGACA | 17973 |
rs52026736 | snp | C/T | | | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100546693 | TGCCCTAGGGGTGAG[C/T]ATGGCAGTGGCACAG | 17973 |
rs52259737 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100505133 | TGAGGCCAGTGAGTT[C/T]TAAGATATCCAGGAA | 17973 |
rs107767601 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100539645 | GGACAGCCAGGGCTA[C/T]ACAGAGAAACTCTGT | 17973 |
rs107857036 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100536481 | ATATGCACCTGGAGC[C/T]ATGGGTCCCACCATT | 17973 |
rs108038495 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100539650 | GCCAGGGCTATACAG[A/C]GAAACTCTGTCTCAA | 17973 |
rs108520863 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100536461 | GTCCCACCATTCTTG[C/T]TCTTTGGTTTGTGGT | 17973 |
rs108545154 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100536494 | AATTCTCTGCTACAT[A/G]TGCAGCTGGAGCCAT | 17973 |
rs211741561 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100541095 | TGAATGGCCTTGTCT[A/G]TGCTGGGAACTGAAC | 17973 |
rs212144414 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100498881 | TTAAACCCTTGCTCT[A/C]TCTGGAATCTTAACA | 17973 |
rs212263893 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100498160 | TCTCCTGCTAAAGCC[-/A]AGAAATAACTGCATA | 17973 |
rs212273574 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100532614 | TTACAATATGAATCA[A/G]TATTTCATTACTTTT | 17973 |
rs212275292 | snp | A/C | | | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100507792 | AGGAGGCCAGGCTTC[A/C]TCCTACATACTTCCT | 17973 |
rs212386808 | in-del | -/ACTCTAAG | | | intron-variant | Nck1 | GRCm38.p3 | 9:100504177 | GCCCTCACCTGAGTA[-/ACTCTAAG]ACTTGAATCAAGGCC | 17973 |
rs212390486 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100522983 | GGAATTCTAGTGAAA[A/C]TCCTGTTTCTTCAAC | 17973 |
rs212550277 | in-del | -/A | | | intron-variant | Nck1 | GRCm38.p3 | 9:100524460 | TGACTTCATGGGTTT[-/A]AAAAAAAAAAAAGGT | 17973 |
rs212629592 | in-del | -/A | | | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100508996 | AATTCCCAATACTAT[-/A]AAAAAGAAATAAATT | 17973 |
rs212667418 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100542026 | TAAACAAATAAAAAA[A/G]CAAGCCATACTAACC | 17973 |
rs212727292 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100531697 | ATCTTCTCCCCCAAA[A/G]ATACATTTTAAACTA | 17973 |
rs212743389 | snp | G/T | | | intron-variant | Nck1 | GRCm38.p3 | 9:100499375 | GGTGGATTGGGACAA[G/T]GAAGAAAAATCAAAA | 17973 |
rs212760941 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100526306 | CAGATGTTGGGGCTA[C/T]CTCCACCAGCAGCTA | 17973 |
rs212798052 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100527084 | CATTTTTTAGAAATG[C/T]ATAAATTTCTACAAA | 17973 |
rs212800985 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100538018 | CTTAACTCCAGTTTC[A/G]AAGATCTAACTCTTT | 17973 |
rs212859244 | in-del | -/AAATTTTTT | | | intron-variant | Nck1 | Mm_Celera | 9:100532896 | AGGAAATGTTATGTA[-/AAATTTTTT]AAATTTTTATAAAAC | 17973 |
rs212941269 | snp | A/C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100528789 | CTCCTTAGAGGAAGT[A/C/T]GTTGTTGACCAGTGA | 17973 |
rs212963463 | snp | G/T | | | intron-variant | Nck1 | Mm_Celera | 9:100538807 | TGTTGAGTGGCATGT[G/T]GTCCTATTAACATAC | 17973 |
rs212964437 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100507204 | TCTGGGGAAAGGGGA[A/G]GTTAGATATTTGAAC | 17973 |
rs212978044 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100516286 | ATTTGCTTTATTCAC[C/T]CTCATTTCAAAGTAA | 17973 |
rs212991523 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100519674 | TCAACTATTGGATGG[A/C]TCACACGGCCCCCAA | 17973 |
rs213056498 | in-del | -/ATTG | | | intron-variant | Nck1 | Mm_Celera | 9:100545126 | GGCTGAAAGCACACA[-/ATTG]ATTGATTTCCAGGTG | 17973 |
rs213057552 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100528431 | TGTCTGGTTCAAATC[A/C]GCTGTTCTGGCTCAA | 17973 |
rs213072910 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100537287 | CTATGAAAATCAAAC[A/G]ATGTGATGAATCCCT | 17973 |
rs213457247 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100502854 | TTAAATTTATATTTT[C/T]CCCTTGTCATCTTAT | 17973 |
rs213488548 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100539672 | CTGTCTCAAAAAAAA[A/G]AAAAAAAAATTCAAA | 17973 |
rs213525992 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100513244 | AGCCCTTGGAAGAGA[C/T]TAATGGAGTTCTAAT | 17973 |
rs213552599 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100514373 | AATGGGAAGGGGGCT[A/G]GAGAGATGGCTCAGC | 17973 |
rs213560415 | in-del | -/T | | | intron-variant | Nck1 | GRCm38.p3 | 9:100503414 | CTAAATATTATTTAC[-/T]TTTTTTTTTTTTAGA | 17973 |
rs213577078 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100502269 | TCTGCCTGCTCATTA[C/T]AATACGTAAGTCACA | 17973 |
rs213687077 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100537494 | CTGGAGACACAGCAC[A/T]GTGGTAAGAGCACTT | 17973 |
rs213687235 | snp | C/G | | | intron-variant | Nck1 | Mm_Celera | 9:100522191 | AGGAAGGGGGGGGGG[C/G]ACATCTACAGGGAAA | 17973 |
rs213731050 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100527427 | ACATTTCTCTAGCTG[A/G]TGTGTAAAATAATTT | 17973 |
rs213750821 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100505307 | TTTCATACAAATTTT[A/T]AAAAATTATTTTATT | 17973 |
rs213859704 | in-del | -/G | | | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100548043 | GAAGGTGCTAAAATA[-/G]GCACTGCAGATCTTG | 17973 |
rs213888809 | in-del | -/T | | | intron-variant | Nck1 | Mm_Celera | 9:100520790 | AGCTGTGTCCCAATG[-/T]TTGGTGCCTTCCTGT | 17973 |
rs213896122 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100521250 | AGGAGCACACACACA[A/C]ACACACTCACTCACA | 17973 |
rs213908025 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100539811 | AAGATACCAAAAGAA[C/T]AGGGAACAAAAGCAA | 17973 |
rs213933655 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100528875 | CTCAAGGGGATAACA[A/T]GGCTAAAACAGAGCT | 17973 |
rs214029242 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100516360 | AGAGGATCTGGGTTC[A/T]AGTCCCAGAACCCAC | 17973 |
rs214038588 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100528294 | CTCTCATCTTCTGCA[A/G]CTCTGAACCTAGAAG | 17973 |
rs214077064 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100496261 | TCTTAATTAGGTGGT[A/G]GCAGCTGCAGGTGTC | 17973 |
rs214275033 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100544364 | TGTTAAGGTTTATGT[A/C]TGGGTTCCTGAAAGC | 17973 |
rs214283509 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100516879 | ATTTGTTTTTTGAAA[C/T]TTTAGATGTAAGATA | 17973 |
rs214377009 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100524979 | CTGTATGACCAAGCC[A/G]ATGATCTGGATTAAT | 17973 |
rs214407837 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100530048 | TAGGTATGGTGGTGC[A/T]TACCTGTAATCCCAC | 17973 |
rs214539431 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100507849 | GAAGTAGGCTCCCCC[C/T]ATCTGCCTTACTTAA | 17973 |
rs214601503 | snp | A/T | | | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100546649 | CCTTCATTCCCGGCT[A/T]CCAGTCCTGTGAAAA | 17973 |
rs214642878 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100524130 | GCTCAAGGGTTATGG[A/T]AGAAGAGGGGACAGA | 17973 |
rs214777744 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100500112 | ACATAGGAGTAACAC[C/T]ATACAGAATGAGCAG | 17973 |
rs214805513 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100539427 | GCAAGTACACTGAAG[-/A]AAAAAGGTAAAGTCT | 17973 |
rs214819609 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100531530 | TCCTGGCAGGAATAA[C/T]CACATCCTGGAATGC | 17973 |
rs214829149 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100533811 | GATAGGTGTGTAGAA[A/G]TGCATTCACTGTCTG | 17973 |
rs214908020 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100500992 | TAAATTCTTAATCCA[A/G]ATGACTTTTAATCCT | 17973 |
rs214909263 | in-del | -/AAC | | | intron-variant | Nck1 | Mm_Celera | 9:100498803 | CAAAAAACAAAAAAA[-/AAC]CAAAAAAACCCCATA | 17973 |
rs215011377 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100515541 | ATAACCAGGTAAAGT[-/A]AAAAAATCAACAAAA | 17973 |
rs215046271 | snp | G/T | | | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100546359 | CCCTGTTCTCCCCTA[G/T]CCTCCTCGGTGGCTG | 17973 |
rs215048296 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100535203 | GTTAGCTGGCTTAGA[C/T]AGAAAGAACCAAAAC | 17973 |
rs215104926 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100536408 | ATCAACCAACCAGGA[C/T]TTCCCCCTACCCCAC | 17973 |
rs215118028 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100544439 | GGCATCAGTTGTGAA[A/G]GGAAGACTTTGAAGT | 17973 |
rs215174947 | in-del | -/TAAAAGTTT | | | intron-variant | Nck1 | Mm_Celera | 9:100532894 | ATAGGAAATGTTATG[-/TAAAAGTTT]TAAAATTTTTATAAA | 17973 |
rs215235030 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100538564 | ACACTACTGAAGTCA[C/T]AGAAAAGTAAGACCA | 17973 |
rs215238221 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100536623 | GGTGGTGGGGAAGCT[C/T]CCTCATAGAACCGGA | 17973 |
rs215259152 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100545028 | CGATGTGAAGAGAAT[A/G]TCTATTTAAAAACAA | 17973 |
rs215290121 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100528326 | CTTCAGCTTCCAGAT[C/T]CCGTCTGCTAACCTA | 17973 |
rs215301921 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100543822 | AAAATAGAACTTTAG[-/A]CTGATGATACACCTC | 17973 |
rs215318711 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100545316 | TTCCTAACTCCTGTG[A/G]ATTCTTTCCTAACTA | 17973 |
rs215360571 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100505950 | TAGAAGGGAGAATGT[-/A]AGGAATCGGTCAGCC | 17973 |
rs215366777 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100537682 | AATAAATAAAGATAA[A/G]GAAAATTTTGGAACT | 17973 |
rs215439156 | in-del | -/AAA | | | intron-variant | Nck1 | Mm_Celera | 9:100535930 | AACTAATTAGAGCTG[-/AAA]AAAAAAAAAAAAAAC | 17973 |
rs215567696 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100496576 | ATTTATCAGGAAAAA[A/G]AATTTTTAAAAAACA | 17973 |
rs215589536 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100543224 | AAAAAGCAAGGGGAA[A/G]AAAAAAGTCAGCTGG | 17973 |
rs215647335 | in-del | -/ATTA | | | intron-variant | Nck1 | Mm_Celera | 9:100514464 | AACTCGCCACTGTCT[-/ATTA]ACTCCAGCTCCAGAG | 17973 |
rs215708872 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100542159 | CCAGTACCTGGGAGG[C/T]AGAGACAGGAGGATG | 17973 |
rs215744451 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100496171 | TATCAGGCTGGCCTC[A/G]AACTCAGAAATCCGC | 17973 |
rs215820264 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100502602 | CTCAGTTATTAAGGA[A/G]AACTGAATGAACCAA | 17973 |
rs215823137 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100512784 | CCAAAGCTGACACCT[A/G]ACAACCATGTGCAGA | 17973 |
rs215858343 | in-del | -/T | | | intron-variant | Nck1 | Mm_Celera | 9:100501610 | AATGACCCTGTTTGA[-/T]CCCGGCATGATGGAA | 17973 |
rs215942856 | in-del | -/AAAAAAA | | | intron-variant | Nck1 | GRCm38.p3 | 9:100542059 | CCAAAACATATCTGG[-/AAAAAAA]AAAAAAAAAAAGCTT | 17973 |
rs215953241 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100500047 | ACACCTTCCCCAAGA[A/C]GAGCACACTGGTTAA | 17973 |
rs216036450 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100537152 | CAGAGCCAGGCCTGG[A/G]AGATAGAACTCAGTA | 17973 |
rs216149443 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nck1 | GRCm38.p3 | 9:100507916 | TAGAGAAAGAAAGAC[A/G]TCAACAAAAGTGCAA | 17973 |
rs216229432 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100498333 | AAATGAAACAACTAT[C/T]TAAATTAGTACCTGT | 17973 |
rs216313465 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100533692 | GATGCACTGCTGTCT[C/T]GCCTGCTGATTTATG | 17973 |
rs216315341 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100516407 | CTTCTGACCTACATA[A/G]GCACCAAACAAGTCC | 17973 |
rs216362997 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100523864 | ACACACAcacaaatc[A/C]tatgttgaaatccaa | 17973 |
rs216364978 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100533772 | CTATGCGTGCGTGCG[C/T]GCGTGCGTGTGTGTG | 17973 |
rs216422832 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100516860 | TGCTCCTTCCCTACT[C/T]TCTATTTGTTTTTTG | 17973 |
rs216428971 | in-del | -/AAAAAA | | | intron-variant | Nck1 | Mm_Celera | 9:100496852 | GTCATTCTCTCATTT[-/AAAAAA]AAAAAAAAAAAAAAA | 17973 |
rs216503974 | in-del | -/AGAA | | | intron-variant | Nck1 | Mm_Celera | 9:100535204 | TTAGCTGGCTTAGAT[-/AGAA]AGAACCAAAACAAGC | 17973 |
rs216506654 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100518326 | CAGCATTTTCAACAA[A/T]TGGTGCTGGCACAAC | 17973 |
rs216543188 | in-del | -/T | | | intron-variant | Nck1 | Mm_Celera | 9:100528855 | TCAGCTCCTCAGACA[-/T]CTGGCTCAAGGGGAT | 17973 |
rs216735478 | in-del | -/GTCCAGCTTCACT | | | intron-variant | Nck1 | Mm_Celera | 9:100543519 | TGTGACCCCCTGTAA[-/GTCCAGCTTCACT]GTATCTGACACTTTC | 17973 |
rs216991884 | in-del | -/AAA | | | intron-variant | Nck1 | Mm_Celera | 9:100524459 | TGACTTCATGGGTTT[-/AAA]AAAAAAAAAAAAAGG | 17973 |
rs217021627 | in-del | -/ATAT | | | intron-variant | Nck1 | Mm_Celera | 9:100504663 | TTATTATAAATACAA[-/ATAT]ATATATATATTACAG | 17973 |
rs217063803 | in-del | -/AG | | | intron-variant | Nck1 | Mm_Celera | 9:100511245 | GACATACAGACAGAC[-/AG]AGACAGAGACAGAGA | 17973 |
rs217072702 | snp | A/G | | | downstream-variant-500B | Nck1 | Mm_Celera | 9:100494836 | GTACTTGAGGTGTGG[A/G]GGACACTCCCTAAAT | 17973 |
rs217142496 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100508765 | CATTTAAGAGGCCAG[A/G]AATTATGACTCATAC | 17973 |
rs217409283 | snp | C/G | | | intron-variant | Nck1 | Mm_Celera | 9:100528712 | AAATTCCTCCATACA[C/G]TATTGAGAGGTCTAA | 17973 |
rs217411333 | in-del | -/AAA | | | intron-variant | Nck1 | Mm_Celera | 9:100527464 | GCTAATAAAGAGATT[-/AAA]AAAAAAAAAAAAAAA | 17973 |
rs217433183 | in-del | -/AAAAAACA | | | intron-variant | Nck1 | Mm_Celera | 9:100498790 | TCTACATTAAAAAAC[-/AAAAAACA]AAAAAACAAAAAAAC | 17973 |
rs217598188 | in-del | -/AAC | | | intron-variant | Nck1 | Mm_Celera | 9:100506324 | AAATTCAGTAAACAA[-/AAC]AACAACAAAAACCAA | 17973 |
rs217604922 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100541061 | TCAGATCTTCAGGAA[A/C]AAGAGGGACAGACAG | 17973 |
rs217614101 | snp | G/T | | | intron-variant | Nck1 | Mm_Celera | 9:100523159 | CTCAGGGGCTGCTCT[G/T]CCACAGAAAGGACCC | 17973 |
rs217710661 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100544283 | TCAGAAACTGAAAAA[C/T]AATATATAAGAATAC | 17973 |
rs217717482 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100512500 | GTTAAGAAACTTTTA[C/T]TGTATAAAAGCATTC | 17973 |
rs217777186 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100543371 | AAGACTCAGTTTAAC[A/T]TAGGTAACAGAAAAT | 17973 |
rs217846314 | in-del | -/AG | | | intron-variant | Nck1 | Mm_Celera | 9:100499292 | TCCCTCCCCCAGTGC[-/AG]AGTTACTCTGAGGAT | 17973 |
rs217847544 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100508920 | ATACAAAACAGGAGA[C/T]GGGCGGGGCACTATG | 17973 |
rs217849825 | in-del | -/C | | | intron-variant | Nck1 | Mm_Celera | 9:100525141 | TCCTTTAAGTGGTCT[-/C]CCTGTTCCCAGTCTC | 17973 |
rs217985363 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100505994 | AGGAGACAAAAGCCC[A/C]CACACTGCAATGGCC | 17973 |
rs218119886 | in-del | -/TAA | | | intron-variant | Nck1 | Mm_Celera | 9:100534270 | AAATCACATAATTAT[-/TAA]AAAAAAAAAAAAAAG | 17973 |
rs218251998 | in-del | -/TGGTATTCC | | | intron-variant | Nck1 | Mm_Celera | 9:100539946 | ACTATTCCTCTAACA[-/TGGTATTCC]CATAAAAATTCAAAC | 17973 |
rs218258762 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100516479 | TTAAAAACATTTTTT[A/C]AAAACAAAACCACTG | 17973 |
rs218284877 | in-del | -/ACA | | | intron-variant | Nck1 | GRCm38.p3 | 9:100530292 | ATGTGCCACCCCCCC[-/ACA]CACACACACACACAC | 17973 |
rs218293220 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100520058 | TAATTCATTGGTTTA[C/T]ATAAAAAAGGACTCT | 17973 |
rs218359980 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100510848 | TGAGAAAAACATAGA[C/T]GAGCAGAGAAATTTG | 17973 |
rs218394768 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100499326 | TACCTAACAGACCTC[A/G]GACCTCTGATTCCAG | 17973 |
rs218499245 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100500100 | CCCTGCAAACATACA[C/T]AGGAGTAACACTATA | 17973 |
rs218565273 | in-del | -/AGGTGT | | | intron-variant | Nck1 | Mm_Celera | 9:100513737 | ACTGTCAAAAAAAGA[-/AGGTGT]AGGTGTGTGTGTGTG | 17973 |
rs218608548 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100524284 | CAAAATCTCAATGTG[A/G]AGGGGAGGGACACAA | 17973 |
rs218740330 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100544986 | AAGTACTAATCAACC[-/A]ACGCATACGCTTTGA | 17973 |
rs218813949 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100496789 | TACGTTCAAGGCACC[A/C]TGGTCTACCTACACA | 17973 |
rs218890911 | snp | G/T | | | intron-variant | Nck1 | Mm_Celera | 9:100516088 | CATTTTCACCTAACA[G/T]AGACCAATAATTTAG | 17973 |
rs218899151 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100500422 | GGCAGTGTATAAAGA[A/G]ATAATATATAATGAT | 17973 |
rs218993275 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100527659 | AGTAGGTCTCCTTTA[A/C]TTTTTCATCTTGGTA | 17973 |
rs219024608 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100513494 | TTTTCTTTATAAACT[A/G]CCTAAGCTTTAAGTA | 17973 |
rs219036384 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100499897 | GACATCAGACAGAAG[-/A]AAAAAAAATGAAGTC | 17973 |
rs219092306 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100526752 | TATTTGTAATCTCTC[A/G]GTTCTGAGGACATGA | 17973 |
rs219136992 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100506095 | TTAGGCTTTCTGACT[A/C]TTAAGAGACTTCTAG | 17973 |
rs219278812 | in-del | -/GAAA | | | intron-variant | Nck1 | Mm_Celera | 9:100543221 | ATTAAAAAGCAAGGG[-/GAAA]AAAAAAGTCAGCTGG | 17973 |
rs219348331 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100521390 | GAGGGCCTGGATTGC[C/T]TCAATGAAAACCCCC | 17973 |
rs219378450 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100507609 | AGTATGTCAGTCATG[C/T]TACATTTAGTCCCAA | 17973 |
rs219430396 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100511087 | AGAGTTGGGCACAGA[A/C]AATTCCTAGGAGGTA | 17973 |
rs219584803 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100541865 | ACTGGGAATAAAGGT[A/G]TGCACCACTATAACT | 17973 |
rs219623307 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100504432 | CACTCTGTTCTTCTG[C/T]TCTCACGTCTTCAAA | 17973 |
rs219650675 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100538058 | ACAACAAGACCCAGG[C/T]GCCTGGTGCACATAC | 17973 |
rs219656132 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100519362 | GCGAGATATAAGGTG[C/T]AATATGCAAAACATA | 17973 |
rs219657139 | snp | G/T | | | downstream-variant-500B | Nck1 | Mm_Celera | 9:100494540 | TCGAAAAATGTTGTT[G/T]TTTTCCAGTAAATCT | 17973 |
rs219669120 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100529150 | CATACTTCTTGATTC[C/T]GGAGTCTTCCTTCAG | 17973 |
rs219706067 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100539026 | AGAGCATTTTAGCAT[A/G]TCTGTATATCAACAG | 17973 |
rs219769029 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100523580 | ATAACTGATGGGGTC[-/A]AAGGATGTAGCTCTG | 17973 |
rs219861334 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100540044 | CCAACACTCCAGAGG[C/T]TGAGGGGAAAAGATT | 17973 |
rs219873048 | in-del | -/ATATATATATAT | | | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100547594 | AAAACAAAAAGACAA[-/ATATATATATAT]ATATATATATATGCA | 17973 |
rs219936751 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100519922 | GGGTGGGGAGAGGGT[A/G]GGGGACTTTTGGGAT | 17973 |
rs219960490 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100535076 | CTAAGATGACAAAGC[-/A]AAGAGCAATAGGATT | 17973 |
rs220043065 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100514542 | CACATAAATTTTTTT[A/T]AAAAATTAAAAGAAA | 17973 |
rs220070899 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100539264 | ATACAGAGAAAACCT[A/G]TCTCAAAAAACAAAA | 17973 |
rs220142915 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100522116 | ATTGGCATAGGTCAT[A/G]AGCAATGGGACCCTT | 17973 |
rs220260086 | in-del | -/G | | | intron-variant | Nck1 | Mm_Celera | 9:100540586 | CAGAGTAGGATTCAA[-/G]TACTAAACTATCTGA | 17973 |
rs220418617 | snp | A/G | | | intron-variant, utr-variant-5-prime | Nck1 | Mm_Celera | 9:100545723 | CGGAGAACCGCCGAG[A/G]CAGCGCGCCGCACAC | 17973 |
rs220461535 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100495930 | TATCTACAGTACCCA[A/C]AAAGTAGTGAACACA | 17973 |
rs220490795 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100495818 | TCTTCTTTATTCCTC[A/G]AAATAAACCCTTTTT | 17973 |
rs220555194 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100544615 | ATCCATTCTTCCACA[C/T]TGCCAGAGTTAATTC | 17973 |
rs220625067 | in-del | -/T | | | intron-variant | Nck1 | Mm_Celera | 9:100512528 | TCAAAACTAGAAGGG[-/T]TTTCATATGAGGAGT | 17973 |
rs220686553 | snp | G/T | | | intron-variant | Nck1 | Mm_Celera | 9:100500142 | GATTGTATTAAATAT[G/T]TAAGAACACACACAC | 17973 |
rs220691012 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100533333 | TCTTCCCATTGAGTG[C/T]ACTTCTCTGACCTCT | 17973 |
rs220743805 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100533913 | GGGCATGGTGGCGCA[C/T]GCCTTTGATCTCAGC | 17973 |
rs220780984 | in-del | -/AG | | | intron-variant | Nck1 | Mm_Celera | 9:100512727 | AGTAGGAGAGAGAAC[-/AG]GGCATTAAAAATAGC | 17973 |
rs220840540 | snp | G/T | | | intron-variant | Nck1 | Mm_Celera | 9:100499770 | AGACTTTACAAAAAA[G/T]AATCAAACAATTCCT | 17973 |
rs220851348 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100534045 | GAACCACCCCCCCCC[-/A]AAAAAAAAAAGAGTC | 17973 |
rs220853036 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100501577 | GGCTCTGTGAGTAAA[A/C]GTACTTCCTACCAAT | 17973 |
rs220874184 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100530254 | ACAAAGTTGTCCTCT[A/G]ATTTCTATACATGAA | 17973 |
rs220940722 | in-del | -/C | | | intron-variant | Nck1 | Mm_Celera | 9:100521473 | TTGAGGAGAGATTTT[-/C]TTTTAATTAGACCCC | 17973 |
rs221024610 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100541410 | AGAAACTGATCTAGG[A/G]ACATAGCTCAGGTGG | 17973 |
rs221051466 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100510366 | AGCCACCACTGCCTA[A/G]CTTATATGCATTATT | 17973 |
rs221084584 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100527552 | AGGCAGAATGACTGC[C/T]ATGAGTTTATGGCCA | 17973 |
rs221125927 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100501352 | AAACTTGGCAGAGAT[-/A]ATGTATTTACTCACT | 17973 |
rs221169877 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100526692 | CCAGCACCCATATTT[A/T]AAAAATAAATAAATA | 17973 |
rs221198412 | in-del | -/CAAAG | | | intron-variant | Nck1 | Mm_Celera | 9:100545182 | TCATCATCAAGCTAC[-/CAAAG]CAAAGCTTTTGAAAA | 17973 |
rs221207788 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100505697 | GACGAAACACCTGGG[A/G]TGTGTTGGCAGCACA | 17973 |
rs221251389 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100535465 | GACGTTTCAAAAGCT[A/G]TTCCCAGTTAGTTCC | 17973 |
rs221357352 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100500194 | AAAGAAAAAGAGACC[A/G]TGTATTTCAAGGAGG | 17973 |
rs221415299 | snp | A/G | | | intron-variant, utr-variant-5-prime | Nck1 | Mm_Celera | 9:100545863 | CCGCTCCGCTCCGCC[A/G]CCAGCAGACGGCGCC | 17973 |
rs221478819 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100543612 | AAGCACACACTTTTT[A/T]AAAATGTTTAACAAT | 17973 |
rs221536623 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100513535 | AAAAACACCAACACT[-/A]AAAAAAAAAAAAACC | 17973 |
rs221574244 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100542721 | CCCTCTGTCCATCAC[A/G]GAGCTACATCCCTAG | 17973 |
rs221594393 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100496848 | AATGAGTCATTCTCT[C/T]ATTTAAAAAAAAAAA | 17973 |
rs221598565 | snp | A/G | | | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100548008 | GTTATGCTGTTATAG[A/G]AAAGAGTCTACCTTG | 17973 |
rs221681924 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100540179 | TCTCAGGAGGATTTA[C/T]AGAAGCCAACAAATA | 17973 |
rs221700685 | snp | G/T | | | intron-variant | Nck1 | Mm_Celera | 9:100506317 | TTAAGTAAAATTCAG[G/T]AAACAAAACAACAAC | 17973 |
rs221703940 | snp | A/G | | | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100547336 | CTAGGTAAAATACAA[A/G]TTACCTGTAGCCCCT | 17973 |
rs221890176 | snp | C/G | | | intron-variant | Nck1 | Mm_Celera | 9:100513927 | AATACTAAATGCTCA[C/G]ACAAGTATGCTGAAA | 17973 |
rs221908519 | in-del | -/CACACC | | | intron-variant | Nck1 | Mm_Celera | 9:100521249 | AGGAGCACACACACA[-/CACACC]AACACACTCACTCAC | 17973 |
rs221916896 | in-del | -/TT | | | intron-variant | Nck1 | GRCm38.p3 | 9:100515159 | CAGCAACATGACAGA[-/TT]TTTTTTTTTCTTCAT | 17973 |
rs221964921 | in-del | -/CT | | | intron-variant | Nck1 | Mm_Celera | 9:100525016 | TATTCAGTCACCTCC[-/CT]CTCAACTCGCTGCCC | 17973 |
rs222007431 | snp | A/C | | | intron-variant | Nck1 | GRCm38.p3 | 9:100534044 | GGAACCACCCCCCCC[A/C]AAAAAAAAAAAGAGT | 17973 |
rs222160157 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100537057 | TAACAATAATATCAT[C/T]ATTGCTATTATTATT | 17973 |
rs222228535 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100543475 | GGTTCTTGCAAAAGA[C/T]CCAAGGCTGATTCCC | 17973 |
rs222334725 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100523227 | AGTCCTGACATCCTC[C/T]CACACACAGACAGAC | 17973 |
rs222372151 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100539155 | CTAGGCACACACTTT[C/T]GATCCCAGCACTTTG | 17973 |
rs222418324 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100532034 | ATAAGAAAGCACAAG[C/T]CCCAGGTTCAGGAAG | 17973 |
rs222452674 | in-del | -/ACACACACACACAC | | | intron-variant | Nck1 | Mm_Celera | 9:100525863 | TGTGGGAATTCTGTT[-/ACACACACACACAC]ACACACACACACACA | 17973 |
rs222456168 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100521771 | GAAACTAGCATCCTA[C/T]TATTATAAAATTGCC | 17973 |
rs222485406 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100528498 | CTCAGCTTCTGACTG[A/G]ATTGCTCTGCTTGGA | 17973 |
rs222521034 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100530576 | GCCCATGGTAAAGGA[A/G]GAAATTACATTTAAT | 17973 |
rs222702743 | in-del | -/GAA | | | intron-variant | Nck1 | Mm_Celera | 9:100513587 | GAAAGTATCCTTAAT[-/GAA]GAAGATAAACAATAC | 17973 |
rs222814327 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100533641 | TTTTACCGCTGAGCC[-/A]CCTTGCCATTCCCTG | 17973 |
rs222819490 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100505496 | TCTTGCCAAACCATC[A/G]AGCTGGTTTTTATAC | 17973 |
rs222909851 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100521572 | AAGGGCTTTACTGTA[C/T]GTAAATCAACTAAGT | 17973 |
rs223037098 | in-del | -/C | | | intron-variant | Nck1 | Mm_Celera | 9:100497172 | CACACCTCAGTTTGG[-/C]TTAAGGAAGCCAGCC | 17973 |
rs223040682 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100539999 | TTAAAAGTGGGCAGG[C/T]AGCTGGCTTGCAAGA | 17973 |
rs223042465 | in-del | -/AC | | | intron-variant | Nck1 | Mm_Celera | 9:100521855 | GACCAAAATATCTAT[-/AC]TTCACCTATTTCTAT | 17973 |
rs223043414 | in-del | -/AC | | | intron-variant | Nck1 | GRCm38.p3 | 9:100496589 | AAGAATTTTTAAAAA[-/AC]AACTGTCAAATTTTA | 17973 |
rs223050687 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100499386 | ACAATGAAGAAAAAT[A/C]AAAAAGCTGGAAAAG | 17973 |
rs223058312 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100528567 | CGTGCTGCTCTGAAG[C/T]AGCCTCTCTTTTCTG | 17973 |
rs223079758 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100542304 | AAAACCTTTACCTGG[C/T]AGTTTTCTGTGCTGT | 17973 |
rs223096430 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100528919 | TCTTCAAGGTATCAC[C/T]AAATATAGTGAAACT | 17973 |
rs223162406 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100515512 | TAAGCAATATTTTCA[A/G]ATGTATACACATAAA | 17973 |
rs223183477 | in-del | -/ATCT | | | intron-variant | Nck1 | Mm_Celera | 9:100520508 | AGTTTTCTAAACCTC[-/ATCT]ATCTATCAAATTTAG | 17973 |
rs223205845 | in-del | -/AAA | | | intron-variant | Nck1 | Mm_Celera | 9:100506358 | CAAAATAAAACAAAC[-/AAA]AAAAAAAAACCCTAT | 17973 |
rs223243616 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100528279 | TCTAGTTTCCATACT[A/C]TCTCATCTTCTGCAG | 17973 |
rs223326902 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100514279 | TGCTAACTCTGACTC[C/T]ATTTACATAAAATTC | 17973 |
rs223388153 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100534895 | TAATTTCCTTCCCCC[A/G]TTTTGTTTTGTTTTG | 17973 |
rs223425292 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100543459 | AGTTAAATTCAAGTA[C/T]GGTTCTTGCAAAAGA | 17973 |
rs223478203 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100525355 | GAACTCTTTCAACAC[A/G]AGAGAAACTAAAGTC | 17973 |
rs223562869 | in-del | -/AC | | | intron-variant | Nck1 | Mm_Celera | 9:100500147 | ATTAAATATTTAAGA[-/AC]ACACACACACATACC | 17973 |
rs223643560 | snp | C/G | | | downstream-variant-500B | Nck1 | Mm_Celera | 9:100494613 | AATTACTGACATGAG[C/G]AATTAGTGATGTTTA | 17973 |
rs223694561 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100535353 | TCATCTTCATAAGGC[C/T]ATATATTTGAATGTT | 17973 |
rs223766912 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100527842 | AAAAACAACAGCAAC[A/G]ACAAAAAGAATATTG | 17973 |
rs223943540 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100530249 | ACTGCACAAAGTTGT[A/C]CTCTGATTTCTATAC | 17973 |
rs223968426 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100510599 | TCAACATCCTTTTGC[-/A]TAAGTATGTCAACAA | 17973 |
rs223974432 | in-del | -/AAAAAG | | | intron-variant | Nck1 | Mm_Celera | 9:100519982 | GTAATAAAAAAAAAA[-/AAAAAG]AAAGAAAGAACTACC | 17973 |
rs223984491 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100496099 | ACTAAATTTCCCCCC[A/C]ATCCCCAAGACAGGG | 17973 |
rs223993416 | in-del | -/AA | | | intron-variant | Nck1 | Mm_Celera | 9:100519971 | AAGAAAATACGTAAT[-/AA]AAAAAAAAAAAAAAA | 17973 |
rs224050990 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100508208 | TTGGGCTGGAGAGAT[A/G]GCTCAGAAGTTAAGA | 17973 |
rs224076306 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100524206 | AGACACAATATGGCA[A/G]CTGCATATGAATTCA | 17973 |
rs224105445 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100503326 | TGTAGATCAGGTTGG[C/T]CTCAAACTCAGAAAT | 17973 |
rs224107262 | in-del | -/TTACCTTG | | | intron-variant | Nck1 | Mm_Celera | 9:100521272 | CACTCACAAATTTAC[-/TTACCTTG]TTACCTTGGAACTCA | 17973 |
rs224116782 | in-del | -/CA | | | intron-variant | Nck1 | GRCm38.p3 | 9:100530291 | CATGTGCCACCCCCC[-/CA]CACACACACACACAC | 17973 |
rs224130742 | in-del | -/ACTGAGTG | | | intron-variant | Nck1 | Mm_Celera | 9:100536220 | CTGTCAAAAAATTAC[-/ACTGAGTG]AAAAATTCATCAAGT | 17973 |
rs224218650 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100544948 | TCCCAGAGAAAGCAC[C/T]ACATGTGGCCACGAT | 17973 |
rs224363596 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100500062 | AGAGCACACTGGTTA[A/G]TTCTCCAATGCCAAA | 17973 |
rs224374677 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100525778 | CTTAAAAAGGCAATG[C/T]GAATACCAAGAAAAG | 17973 |
rs224449489 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100535333 | TTGTGATAGTTGAAT[A/G]AGAATCATCTTCATA | 17973 |
rs224529367 | snp | C/T | | | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100546716 | TGGCACAGTCCCAGC[C/T]ACCTGCCAAGGAAGG | 17973 |
rs224731519 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100529532 | AAAAAAAAAAAAAAA[A/G]AAAGTAGTTGCTAGG | 17973 |
rs224782322 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100520578 | ATATCACATCCCCAC[A/G]CAACATGAGTTAAGA | 17973 |
rs224891702 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100498596 | ACAATGTCTTATACT[C/T]TATTACTTGTCTGCT | 17973 |
rs224919490 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100530353 | CACACACACACAGAT[A/C]TGCACACAATAATAA | 17973 |
rs224935341 | in-del | -/T | | | intron-variant | Nck1 | Mm_Celera | 9:100503036 | ATAACAGTTGTCAGG[-/T]TTTTTTTGTTATTTT | 17973 |
rs225000409 | snp | A/T | | | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100546278 | ATCAAGCGCGGGCCC[A/T]GAGTGGTCCCTGAGC | 17973 |
rs225047192 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100509334 | TTTTTAACATATTTA[A/T]CTCAATTAACAAAAC | 17973 |
rs225069318 | snp | C/G | | | intron-variant | Nck1 | Mm_Celera | 9:100521189 | GCAATTAGTGCATTC[C/G]AGATTGGTAAAAGGT | 17973 |
rs225216330 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100511816 | AGAAAGTAGAAAGAC[C/T]GTTGCTTGGAAATGA | 17973 |
rs225227403 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100500034 | ATGCTGAGAGCAGAC[A/G]CCTTCCCCAAGAAGA | 17973 |
rs225285408 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100524938 | CTTAGAAATTTCCTG[C/T]TGCAACCCACCCTAA | 17973 |
rs225285626 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100514799 | GCTAAGCCTCTGAGA[A/G]AACATATCCTCCCTC | 17973 |
rs225297882 | in-del | -/TACA | | | intron-variant | Nck1 | Mm_Celera | 9:100513309 | AGCAAGTGGCCCTGG[-/TACA]TACATAGATCCTTTT | 17973 |
rs225377114 | in-del | -/TC | | | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100507082 | ATGAATACATACATT[-/TC]CTTCATTTCCCTTGA | 17973 |
rs225827861 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100496973 | TATCTCTAGTAGCAG[C/T]TAATTTGCATCATCC | 17973 |
rs225897685 | in-del | -/AAGG | | | intron-variant | Nck1 | Mm_Celera | 9:100537004 | TCAGTTTGTGCTTAA[-/AAGG]AAGGGGGAAAACATA | 17973 |
rs225994309 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100544585 | ATAATCATTTGATTT[C/T]CTGGCATTGAAAGCA | 17973 |
rs226119660 | in-del | -/TGA | | | intron-variant | Nck1 | Mm_Celera | 9:100529864 | AGTTGACTAATATAC[-/TGA]TGATATAAATAGAAA | 17973 |
rs226121872 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100511963 | TTAGGTCATTCTTTT[A/T]CTGTTATTTTCAGTT | 17973 |
rs226131564 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100510465 | TGCTTTCTTCAGAGA[A/G]ATTGTTTCATAAAAG | 17973 |
rs226155255 | snp | G/T | | | intron-variant | Nck1 | Mm_Celera | 9:100498963 | GTATTCATGTCCAAA[G/T]AAAAATGATCCCTCC | 17973 |
rs226202071 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100541290 | TTCCAATCCCCTGTT[A/T]ATGTTTCTGCAATAG | 17973 |
rs226211326 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100498538 | CTTACCGTGACATTT[A/G]CTCACTCCTGTGTTT | 17973 |
rs226357063 | snp | G/T | | | intron-variant | Nck1 | Mm_Celera | 9:100543773 | CTGTCCTGACTCTGG[G/T]TGTAGAAAATATAAT | 17973 |
rs226416306 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100505829 | GTACCCACATGCACA[C/T]AGGCTTGTACACACA | 17973 |
rs226417325 | in-del | -/T | | | intron-variant | Nck1 | GRCm38.p3 | 9:100501426 | CTTTTACTATTACAG[-/T]TTTTTTTTTTATTTT | 17973 |
rs226488940 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100516830 | AAGAAATAATTAACT[A/T]GAAATTTTCAAGACT | 17973 |
rs226493838 | in-del | -/CT | | | intron-variant | Nck1 | Mm_Celera | 9:100510317 | CATAGATCTACCTGC[-/CT]CTCTGCCTTCTGAGT | 17973 |
rs226572305 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100521106 | GAAATGGAAATGGTG[A/G]TGTACTTGTAATCCC | 17973 |
rs226794152 | snp | G/T | | | intron-variant | Nck1 | Mm_Celera | 9:100505790 | AGGATGGCACCTGAG[G/T]TTAGCTTTCGGCCTC | 17973 |
rs226894055 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100500510 | AAAACAAAATGCTAA[C/T]TGTAATTTCCAGGGT | 17973 |
rs226910494 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100543181 | CAACAACGTTCCATG[A/C]TATCATGACACAAAT | 17973 |
rs226973310 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100543839 | TGATGATACACCTCA[A/G]AGGTTTATGAGAAGC | 17973 |
rs226977973 | in-del | -/AA | | | intron-variant | Nck1 | Mm_Celera | 9:100514531 | AACACCAATGCACAT[-/AA]AAATTTTTTTTAAAA | 17973 |
rs227104920 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100508076 | GTGCCACATAACATA[A/G]GTTAACAGGATACAA | 17973 |
rs227220537 | snp | A/G | | | synonymous-codon | Nck1 | Mm_Celera | 9:100497555 | AACATCCATTACATC[A/G]CCTTTCTCAAAATTG | 17973 |
rs227258237 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100498643 | AGCTTCCTAGGGACA[A/G]AAAACTAGAATTTCC | 17973 |
rs227291633 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100500679 | TGATAGTATACCTAG[-/A]ATTCAAACCAACCTA | 17973 |
rs227298483 | in-del | -/GT | | | intron-variant | Nck1 | Mm_Celera | 9:100533788 | CGTGCGTGTGTGTGT[-/GT]ACAGACAGATAGGTG | 17973 |
rs227339887 | in-del | -/AAAAAAAAAA | | | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100508347 | AAAATAAATAAATCT[-/AAAAAAAAAA]AAAAAAAAAAAAAGC | 17973 |
rs227405313 | in-del | -/G | | | intron-variant | Nck1 | Mm_Celera | 9:100528600 | GACCTCATGACAGTT[-/G]GACTTATTCTCTCTC | 17973 |
rs227450199 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100528585 | CCTCTCTTTTCTGTC[C/T]GACCTCATGACAGTT | 17973 |
rs227452633 | in-del | -/G | | | intron-variant | Nck1 | Mm_Celera | 9:100532614 | TTACAATATGAATCA[-/G]TATTTCATTACTTTT | 17973 |
rs227538780 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100504451 | CACGTCTTCAAACCT[A/G]CTTCTCCCTTGTGGA | 17973 |
rs227594090 | snp | A/G/T | | | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100547616 | TATATATATATATAT[A/G/T]TGCAGAGACAGGTTC | 17973 |
rs227624736 | snp | C/T | | | intron-variant | Nck1 | GRCm38.p3 | 9:100532391 | GCATGCTTTGCCCTT[C/T]AAGTATGTTTGTCTA | 17973 |
rs227684231 | in-del | -/CTC | | | intron-variant | Nck1 | Mm_Celera | 9:100496239 | GCCACCACCGCCCGG[-/CTC]CTTTTTTCTTAATTA | 17973 |
rs227702057 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100541669 | TATATATAATTTGCA[A/C]ATCACTAAAGATAAT | 17973 |
rs227704701 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100544771 | AGGCAATACATTAAC[A/G]TGTCGACTTATTAAT | 17973 |
rs227713987 | in-del | -/T | | | intron-variant | Nck1 | Mm_Celera | 9:100502352 | AAGCTAAAGACTAAA[-/T]TAATGAGGTTTTTAC | 17973 |
rs227753721 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100541535 | GATCAGGAGGTTCAA[C/T]ACCACCCTCAACTAC | 17973 |
rs227757903 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100534480 | AAGACAGCAAAGTGT[A/G]TCCATTAGAAATCAG | 17973 |
rs227773059 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100531517 | CAGATGCTAGGATTC[C/T]TGGCAGGAATAACCA | 17973 |
rs227824953 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100540965 | CATACCTTTATTGCA[A/C]AATACCAACCCATAT | 17973 |
rs228004112 | snp | G/T | | | downstream-variant-500B | Nck1 | Mm_Celera | 9:100494663 | TATCTCATTGTCTAC[G/T]GTATTCCCCAAACTT | 17973 |
rs228005803 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100538418 | AAAATTAAGTAAAGA[C/T]AAAACATCCATCAAC | 17973 |
rs228058134 | in-del | -/T | | | intron-variant | Nck1 | Mm_Celera | 9:100520535 | TTAGCTAAAATTTGC[-/T]TTTTTTTTTAAACAC | 17973 |
rs228096764 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100539545 | GCCGGGCATGGTGGC[A/G]CACGCCTTTAATCGC | 17973 |
rs228116695 | snp | A/G | | | downstream-variant-500B | Nck1 | Mm_Celera | 9:100494858 | TCCCTAAATTCTTGT[A/G]TTTTTGTTTAAAATG | 17973 |
rs228304374 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100529861 | CTGCAGTTGACTAAT[A/G]TACTGATATAAATAG | 17973 |
rs228318379 | snp | C/G | | | intron-variant | Nck1 | Mm_Celera | 9:100534910 | GTTTTGTTTTGTTTT[C/G]TTTCTTTTTGAGATA | 17973 |
rs228402058 | snp | C/G | | | intron-variant | Nck1 | Mm_Celera | 9:100521055 | GACATGAGGACCTGA[C/G]TTCAAACCACAGAAC | 17973 |
rs228453719 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100510267 | AGCCCTGGCTATCCC[A/G]GAACTCACTCTTGTA | 17973 |
rs228464370 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100516733 | TATTAAAAAAAAAAA[A/G]AAAAGAAAAGAAATA | 17973 |
rs228494563 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100523644 | TGAGCTCAATCATCA[C/T]CACCACATAAAACCA | 17973 |
rs228507397 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100528779 | GCAATCTAGGCTCCT[C/T]AGAGGAAGTTGTTGT | 17973 |
rs228539929 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100540608 | ACTATCTGAGCCAAT[C/T]GGGGACTTTGTCATT | 17973 |
rs228554814 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100529589 | AAATGGGTAAAGAGT[C/T]TTCATACCAAGATGA | 17973 |
rs228605118 | snp | G/T | | | intron-variant | Nck1 | Mm_Celera | 9:100532478 | ATCAGGATAACAGTT[G/T]TGAAACACCATTTAG | 17973 |
rs228684197 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100508421 | TCCTTCAATAAGAAA[C/T]AACTTACCTAAGGTG | 17973 |
rs228686602 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100533495 | TTTTTCTTTTTCTTC[C/T]TTTCGAGAAATGGAA | 17973 |
rs228694356 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100522945 | AAACAAAGGAAGAGA[A/G]ATCAAGTATTCTGCT | 17973 |
rs228725871 | snp | G/T | | | intron-variant | Nck1 | Mm_Celera | 9:100512523 | AAGCATTCAAAACTA[G/T]AAGGGTTTCATATGA | 17973 |
rs228729158 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100498805 | AAAAAACAAAAAAAC[A/C]AAAAAACCCCATATA | 17973 |
rs228744814 | in-del | -/ACACACACACACACACACAC | | | intron-variant | Nck1 | Mm_Celera | 9:100524768 | AGCATCGATGTGTAT[-/ACACACACACACACACACAC]ACACACACACACACA | 17973 |
rs228919092 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100528190 | CTTTTATTTCCTCAG[A/G]TGAAGTGATGAGAGC | 17973 |
rs228969729 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100500674 | CATCACTGATAGTAT[A/C]CCTAGATTCAAACCA | 17973 |
rs228998965 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100537193 | TAGAATGTATGTTTA[A/G]TGGTTCAACCCAGCA | 17973 |
rs229069687 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100527065 | TCAGCTTACTGCTAT[C/T]CTACATTTTTTAGAA | 17973 |
rs229088807 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100537441 | GAAACATACATACAA[C/T]AATAATAATTTTTCA | 17973 |
rs229123225 | snp | G/T | | | intron-variant | Nck1 | Mm_Celera | 9:100543775 | GTCCTGACTCTGGGT[G/T]TAGAAAATATAATAA | 17973 |
rs229195576 | in-del | -/CCAGAATTTAATG | | | intron-variant | Nck1 | Mm_Celera | 9:100511108 | CTAGGAGGTAGCATT[-/CCAGAATTTAATG]CCAGCCCATCTAGCA | 17973 |
rs229200273 | in-del | -/T | | | intron-variant | Nck1 | Mm_Celera | 9:100542008 | GGATTTGGCAGTTTA[-/T]TTTAAACAAATAAAA | 17973 |
rs229231094 | in-del | -/G | | | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100547051 | TGTGTTCGAGTGTTT[-/G]GTGTACTTGTGTTAT | 17973 |
rs229377606 | in-del | -/AA | | | intron-variant | Nck1 | Mm_Celera | 9:100496581 | CAGGAAAAAGAATTT[-/AA]TTAAAAAACAACTGT | 17973 |
rs229424468 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100525989 | ATCAGAATTGACTTA[A/G]ATGTTCACGGGTCTA | 17973 |
rs229631123 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100536219 | ACTGTCAAAAAATTA[C/T]ACTGAGTGAAAAATT | 17973 |
rs229651051 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100535811 | CACATCAAGAGCGGT[A/C]AACAAGATAAGGCAA | 17973 |
rs229697390 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100512956 | TCCTCTGCCCACCAA[A/T]TATCAAAATACATAT | 17973 |
rs229787151 | snp | C/G | | | intron-variant | Nck1 | Mm_Celera | 9:100537142 | CTGTCTAACACAGAG[C/G]CAGGCCTGGGAGATA | 17973 |
rs229816996 | in-del | -/AC | | | intron-variant | Nck1 | GRCm38.p3 | 9:100538820 | TGGTCCTATTAACAT[-/AC]ACACACACACACACA | 17973 |
rs229850388 | in-del | -/A | | | upstream-variant-2KB | Nck1 | GRCm38.p3 | 9:100547374 | CTGAGTTTAGTTGAG[-/A]AAAGTAGAACATAAA | 17973 |
rs229886082 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100499458 | TAAAAGCTCCTGTAT[A/G]TTCTCAGGAACCAAC | 17973 |
rs229925686 | in-del | -/T | | | intron-variant | Nck1 | Mm_Celera | 9:100533145 | AATAATTTTCAGGGA[-/T]CTTTTTTTTAAAGGA | 17973 |
rs229971422 | snp | C/G | | | intron-variant | Nck1 | Mm_Celera | 9:100536885 | tagtcagacTTAAGC[C/G]ACagaaagaaagaaa | 17973 |
rs230020214 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100536861 | AAGATAGGTCTTTTG[-/A]AAAAAATCTAGTCAG | 17973 |
rs230121983 | in-del | -/T | | | intron-variant | Nck1 | Mm_Celera | 9:100496289 | TCATTTTAAACCTAA[-/T]TATTTCTGAATAATG | 17973 |
rs230180575 | snp | A/T | | | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100507576 | GTGCATTGAAATTTT[A/T]AAATACTATTTAATA | 17973 |
rs230316118 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100524104 | AACCTCAGACTTACT[A/G]TCTCACCAAGGCTCA | 17973 |
rs230316512 | snp | A/C | | | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100548013 | GCTGTTATAGGAAAG[A/C]GTCTACCTTGTATGG | 17973 |
rs230420051 | snp | G/T | | | intron-variant | Nck1 | Mm_Celera | 9:100523248 | ACAGACAGACAGACA[G/T]GCAGGCAATAACACC | 17973 |
rs230420242 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100529777 | TTTATATTTAACACC[-/A]AAAAAAATAACCATA | 17973 |
rs230479989 | in-del | -/T | | | intron-variant | Nck1 | Mm_Celera | 9:100506404 | TTGAGAGTAAACAAA[-/T]TTGTTCACAACTGAC | 17973 |
rs230503673 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100519361 | AGCGAGATATAAGGT[A/G]CAATATGCAAAACAT | 17973 |
rs230536669 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100523932 | CAGAATGTAAATGAG[A/G]TAAATGAGTTTACCA | 17973 |
rs230615241 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100534046 | aaCCACCCCCCCCCA[A/C]AAAAAAAAAGAGTCC | 17973 |
rs230628797 | in-del | -/TTTTTTTTT | | | intron-variant | Nck1 | GRCm38.p3 | 9:100514910 | GGGAAGCAAGCCTTC[-/TTTTTTTTT]TTTTTTTTTTTTTTT | 17973 |
rs230636391 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100526860 | TCAAATAAATAAGGA[C/T]GATAACAATAAAGGA | 17973 |
rs230763397 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100543221 | TTAAAAAGCAAGGGG[-/A]AAAAAAAAAGTCAGC | 17973 |
rs230843209 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100534924 | GTTTCTTTTTGAGAT[-/A]AAAAAAATCTCATTA | 17973 |
rs230861613 | snp | G/T | | | intron-variant | Nck1 | Mm_Celera | 9:100496156 | GGAACTCACTCTGTA[G/T]ATCAGGCTGGCCTCG | 17973 |
rs231046216 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100523700 | CCAGAACTGGGGAGG[C/T]AGAGACAGAGGATCC | 17973 |
rs231156382 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100533583 | CTTCTGCCATCTGAG[C/T]TCTAAGGAAGGAACC | 17973 |
rs231166576 | in-del | -/T | | | intron-variant | Nck1 | Mm_Celera | 9:100544309 | AATACAAAGGTAAGA[-/T]TTTTTTTTTAAAGAA | 17973 |
rs231188504 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100510861 | GATGAGCAGAGAAAT[C/T]TGGGGGAGGGAGTGA | 17973 |
rs231250612 | in-del | -/A | | | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100547717 | TGCTATCTCAAAAGC[-/A]AAAAACATACAGGCA | 17973 |
rs231252406 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100531853 | CACATCATAAAACTT[-/A]CCTGCCTAAAATGCA | 17973 |
rs231291400 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100515869 | AAAGCATGTGGGAGA[C/T]AGAGGCAGGAAGGTC | 17973 |
rs231318208 | snp | C/T | | | downstream-variant-500B | Nck1 | Mm_Celera | 9:100494659 | TACATATCTCATTGT[C/T]TACTGTATTCCCCAA | 17973 |
rs231431482 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100544398 | CTACTAATGTATCGC[C/T]AATGAAAGACAGCTT | 17973 |
rs231460087 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100522632 | AGGCTGGCCTTAAAA[C/T]TCACTATATAGGTGA | 17973 |
rs231485264 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100509463 | TGGAACACATAAAAA[C/T]CATCAGTCTGAGGCT | 17973 |
rs231592980 | in-del | -/AGACAG | | | intron-variant | Nck1 | Mm_Celera | 9:100511241 | CTCTGACATACAGAC[-/AGACAG]AGACAGAGACAGAGA | 17973 |
rs231603024 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100522483 | CTAAATATTCTAACT[A/T]ATGAAACACTCTACT | 17973 |
rs231842917 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100537496 | GGAGACACAGCACAG[C/T]GGTAAGAGCACTTGT | 17973 |
rs231947768 | snp | A/G | | | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100546653 | CATTCCCGGCTTCCA[A/G]TCCTGTGAAAAGGAC | 17973 |
rs232043959 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100536625 | TGGTGGGGAAGCTCC[C/T]TCATAGAACCGGAAA | 17973 |
rs232181142 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100516610 | TGTGTATATATATAT[A/G]TATATATATGTTTTT | 17973 |
rs232227899 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100500121 | TAACACTATACAGAA[C/T]GAGCAGATTGTATTA | 17973 |
rs232274261 | snp | C/G | | | intron-variant | Nck1 | Mm_Celera | 9:100500900 | CATGCACTACACCAT[C/G]GAAAACTGTATATGG | 17973 |
rs232321798 | in-del | -/T | | | intron-variant | Nck1 | Mm_Celera | 9:100515571 | CTAAAATGCATTTAC[-/T]TTTTTTTTGTTGGTG | 17973 |
rs232397520 | snp | C/G | | | intron-variant | Nck1 | Mm_Celera | 9:100528295 | TCTCATCTTCTGCAG[C/G]TCTGAACCTAGAAGG | 17973 |
rs232472703 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100501882 | CATGATGGAATGGGG[-/A]AACAAGCATCCATAA | 17973 |
rs232588294 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100512463 | CATTAGCAGAAATGA[A/G]CAGGCCTAATCAGAC | 17973 |
rs232627719 | in-del | -/TAAA | | | intron-variant | Nck1 | Mm_Celera | 9:100530892 | CTCACATACACTAAG[-/TAAA]TAAATAAATAAATAA | 17973 |
rs232639863 | snp | C/G | | | intron-variant | Nck1 | Mm_Celera | 9:100528651 | GCACAGACCTAGAAG[C/G]TCTTTGGATGTGATC | 17973 |
rs232751327 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100504388 | AGAGAAAGTATTGCC[A/G]CTTCTAATTCCTCCC | 17973 |
rs232784102 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100515925 | CAGAACTACACAGGA[A/G]GATCCTGTCTCAAAC | 17973 |
rs232811655 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100496115 | ATCCCCAAGACAGGG[A/T]TTCTCTGTACAGCCC | 17973 |
rs232852843 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100505268 | GATCATCTAACTCCC[A/T]AACAGATTCTGCAAG | 17973 |
rs232915666 | snp | G/T | | | intron-variant | Nck1 | Mm_Celera | 9:100528662 | GAAGGTCTTTGGATG[G/T]GATCCCTTGGCAGAG | 17973 |
rs232940079 | snp | C/G | | | intron-variant | Nck1 | Mm_Celera | 9:100544488 | TAAAGTGAGAATCAG[C/G]CAGGCCTGTCAAATT | 17973 |
rs232986768 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100499196 | ATCTGGTGAAGAAAG[C/T]GAAGTGGCAGGGCAA | 17973 |
rs233066801 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100540347 | ATCCAGGTAACTTAC[A/T]AAGACTGTTGGTTTG | 17973 |
rs233173429 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100521349 | TTATCTGTCTGTACC[A/T]CAGATAATGAATGGT | 17973 |
rs233322663 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100512765 | CTGGAAACCCCTCTC[C/T]CTACCAAAGCTGACA | 17973 |
rs233379249 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100542972 | AGTGTTGGATCTCTA[A/G]GGGGAAAACACAAAA | 17973 |
rs233448877 | snp | C/G | | | intron-variant | Nck1 | Mm_Celera | 9:100502228 | CAATATTACTTTCCC[C/G]CAAAATTCCACCTAT | 17973 |
rs233470571 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100532922 | AAAACTTTTAAAATG[A/G]CACTTGTTTCCTGAA | 17973 |
rs233542905 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100512814 | AATGGGTTCAATCTT[C/T]AGCACAAAAACAAAC | 17973 |
rs233571147 | in-del | -/AAACAAACAAAC | | | intron-variant | Nck1 | Mm_Celera | 9:100511848 | CCAGAACTGATTTAA[-/AAACAAACAAAC]AAACAAACAAACAAC | 17973 |
rs233585739 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100542164 | ACCTGGGAGGCAGAG[A/C]CAGGAGGATGTTTTG | 17973 |
rs233637909 | in-del | -/CT | | | intron-variant | Nck1 | Mm_Celera | 9:100534527 | CTTTGAGCACTAGGA[-/CT]CTCTCTGTTTTGCCT | 17973 |
rs233656573 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100531989 | ACACTTGCTTAGCAT[C/T]CTAACTCTGATTGTT | 17973 |
rs233752574 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100499188 | ATCATGGAATCTGGT[A/G]AAGAAAGCGAAGTGG | 17973 |
rs233756966 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100505123 | TCTGTGAGTTTGAGG[C/T]CAGTGAGTTCTAAGA | 17973 |
rs233764034 | in-del | -/G | | | intron-variant | Nck1 | Mm_Celera | 9:100505367 | TACGTGTATGTATGT[-/G]GCACATGAATATGCT | 17973 |
rs233888404 | snp | C/G | | | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100546383 | GTGGCTGCTTACTTT[C/G]CGCCTCTCCCACTGC | 17973 |
rs233889355 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100539060 | TGTAACCACAATAGA[A/G]AGAATACATTTTTAT | 17973 |
rs233943571 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100539965 | AAAAATTCAAACAAT[C/T]CAACCTCAAATATTA | 17973 |
rs234073596 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100518367 | CATGTAGAAGAATGC[A/G]AATCGATCCATACTT | 17973 |
rs234128549 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100503763 | ACCTCTGGAAGAGTA[A/G]TCAGTGGTCTCATCC | 17973 |
rs234371399 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100501187 | GGAAGAAATCTAAGG[A/G]CATGGTACAGTTTCC | 17973 |
rs234486760 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100521391 | AGGGCCTGGATTGCC[A/T]CAATGAAAACCCCCA | 17973 |
rs234532253 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100541952 | TACATAGTCCAAGCT[A/T]ACCTCAAACCTGTAA | 17973 |
rs234661557 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100531621 | AAGGGTTACAGTACT[A/G]AGTACTTTGCCTTAA | 17973 |
rs234737050 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100528983 | ATTGCTTTGCTGGCT[A/C]CCAATCAATCATATT | 17973 |
rs234776970 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100530177 | AAAGGCACTTGTCAC[A/G]CAAGCCTGGAGACTG | 17973 |
rs234779729 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100501839 | GGCATGATGGAATGG[A/G]GATCCGGCATGATGG | 17973 |
rs234815455 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100539673 | TGTCTCAAAAAAAAG[A/G]AAAAAAAATTCAAAA | 17973 |
rs234817046 | in-del | -/AAAAA | | | intron-variant | Nck1 | Mm_Celera | 9:100498796 | TAAAAAACAAAAAAC[-/AAAAA]AAAAAAACAAAAAAA | 17973 |
rs234834702 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100505456 | ATCATATGGGTTGTC[C/T]GGCTTGATGACAAGT | 17973 |
rs235007960 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100504433 | ACTCTGTTCTTCTGC[C/T]CTCACGTCTTCAAAC | 17973 |
rs235089242 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100525093 | TCTGGCCATATACAT[A/G]AGGAGCCAAGCAGCT | 17973 |
rs235151374 | in-del | -/CTCTGAGG | | | intron-variant | Nck1 | Mm_Celera | 9:100509534 | GCAGCAGCATCACAA[-/CTCTGAGG]CTCTGAGGCCTAGAC | 17973 |
rs235155097 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100533920 | GTGGCGCACGCCTTT[A/G]ATCTCAGCACTCGGG | 17973 |
rs235210393 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100535217 | ATAGAAAGAACCAAA[A/G]CAAGCAAAAAACCAA | 17973 |
rs235239724 | in-del | -/G | | | intron-variant | Nck1 | Mm_Celera | 9:100512657 | GGAACTTTTACTACA[-/G]GGGAGTACTGTCCTT | 17973 |
rs235346564 | snp | G/T | | | intron-variant, utr-variant-5-prime | Nck1 | Mm_Celera | 9:100545608 | AGGATGTCCCCCCTC[G/T]CGGCTTCCTCAGGCT | 17973 |
rs235371169 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100543432 | ATTTCTAGGGACTGG[A/G]AAGATGTCTCCAGTT | 17973 |
rs235497801 | in-del | -/AAAA | | | intron-variant | Nck1 | Mm_Celera | 9:100544964 | CATGTGGCCACGATG[-/AAAA]AAAAAAAAGTACTAA | 17973 |
rs235511726 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100535281 | GTATAGCGGGAATAT[A/G]AAGAAGACACTGCAT | 17973 |
rs235632383 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100536537 | ATCAGGAGGAGAAGA[A/G]GTCCTTGGTCCTGTG | 17973 |
rs235657273 | in-del | -/G | | | intron-variant | Nck1 | Mm_Celera | 9:100540445 | GAACAGAAGCTAAGA[-/G]ACTAATCACATATTC | 17973 |
rs235697730 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100514001 | ATATGATAGAAGACT[A/G]TCAGTTTCTACTAAC | 17973 |
rs235832768 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100499329 | CTAACAGACCTCGGA[C/T]CTCTGATTCCAGAGC | 17973 |
rs235855197 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100511433 | TATTTTGATACTTGA[C/T]AACTGTCTTGAATTT | 17973 |
rs235924593 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100524148 | AAGAGGGGACAGAAA[A/G]ACTGCAAAAGCCAGA | 17973 |
rs235933406 | snp | A/C | | | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100508081 | ACATAACATAGGTTA[A/C]CAGGATACAAAGGAA | 17973 |
rs235975801 | snp | G/T | | | intron-variant | Nck1 | Mm_Celera | 9:100511090 | GTTGGGCACAGAAAA[G/T]TCCTAGGAGGTAGCA | 17973 |
rs236020015 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100502023 | AAACAAATGTATGTG[A/T]AACAGTAGGTTGTAT | 17973 |
rs236094502 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100533838 | TCTGGAGCAACTTCT[A/T]ATACAGGCATGAGCT | 17973 |
rs236101757 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100502933 | ATATTGATATGTATA[A/T]AACTATATTACAAAG | 17973 |
rs236178360 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100536580 | CCCAGTGTAGGGGAA[C/T]GCTAGTGCACTGAGG | 17973 |
rs236198650 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100500159 | AAGAACACACACACA[C/T]ACCAACACCACCAAC | 17973 |
rs236222734 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100520904 | GTACAAACACAGCAA[C/T]AAACAGCTAACTAGA | 17973 |
rs236227718 | in-del | -/A | | | intron-variant | Nck1 | GRCm38.p3 | 9:100514159 | ACAAACGACTGCCTT[-/A]AAAAAACTAGTAAAG | 17973 |
rs236259272 | snp | A/G | | | intron-variant | Nck1 | GRCm38.p3 | 9:100545178 | ATTGATCATCATCAA[A/G]CTACCAAAGCTTTTG | 17973 |
rs236285847 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100502275 | TGCTCATTATAATAC[A/G]TAAGTCACACAGCTT | 17973 |
rs236365245 | in-del | -/G | | | intron-variant | Nck1 | Mm_Celera | 9:100503034 | AGATAACAGTTGTCA[-/G]GTTTTTTTTGTTATT | 17973 |
rs236417984 | in-del | -/ACACACACACAC | | | intron-variant | Nck1 | GRCm38.p3 | 9:100524769 | AGCATCGATGTGTAT[-/ACACACACACAC]ACACACACACACACA | 17973 |
rs236430679 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100528433 | TCTGGTTCAAATCCG[C/T]TGTTCTGGCTCAAAC | 17973 |
rs236477400 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100528366 | TGTCTCAGCCTTCAA[A/G]ACTTACTGCTGGATA | 17973 |
rs236513595 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100513978 | TGATAAAAAATAAAA[C/T]GCTACAGATATGATA | 17973 |
rs236549941 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100537907 | AGAAACAGATTTTTG[A/G]AGCTAGAGAGACATC | 17973 |
rs236591463 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100538985 | ACAAGCTGAAATAAA[C/T]CCATTCCTCTGAGCC | 17973 |
rs236597022 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100527597 | TTACAGTCAGCCTAA[A/G]CTAGAGTTCTGAAGA | 17973 |
rs236615425 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100538640 | CTACCCCATCTTGTG[A/G]AAGTATCCTTGTTAG | 17973 |
rs236666609 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100542037 | AAAAACAAGCCATAC[C/T]AACCAACCAAAACAT | 17973 |
rs236666864 | in-del | -/T | | | downstream-variant-500B | Nck1 | Mm_Celera | 9:100494731 | ATCTATAGACCATAC[-/T]TTGATCAAAGAACCT | 17973 |
rs236699966 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100529304 | AAATTTATTGAAAGG[-/A]AAAAAAAACAGATTA | 17973 |
rs236795294 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100524285 | AAAATCTCAATGTGG[A/C]GGGGAGGGACACAAA | 17973 |
rs236957660 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100544332 | TTAAAGAAAACAACT[A/T]CAAAAAAACAGTACA | 17973 |
rs237039272 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100533774 | ATGCGTGCGTGCGTG[C/T]GTGCGTGTGTGTGTA | 17973 |
rs237099419 | in-del | -/ACACACACACACACACACAC | | | intron-variant | Nck1 | GRCm38.p3 | 9:100537382 | CACAGCAGCAAGCAA[-/ACACACACACACACACACAC]ACACACACACACACA | 17973 |
rs237185832 | snp | G/T | | | intron-variant | Nck1 | Mm_Celera | 9:100498230 | GGTTTACTTCTTTCA[G/T]AGCTACAACTAAGAA | 17973 |
rs237339502 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100513676 | GAAATAGACCAGAAT[C/T]TACATAGCAAATTCT | 17973 |
rs237436922 | in-del | -/GGGG | | | intron-variant | Nck1 | Mm_Celera | 9:100530714 | TTTCTAAAAGATAGC[-/GGGG]GGGGGGGGGGGGGGC | 17973 |
rs237456288 | snp | G/T | | | intron-variant | Nck1 | Mm_Celera | 9:100500106 | AAACATACATAGGAG[G/T]AACACTATACAGAAT | 17973 |
rs237675175 | snp | C/G | | | intron-variant | Nck1 | Mm_Celera | 9:100526773 | GAGGACATGAAGGCA[C/G]AAGGATCTCTGGTTT | 17973 |
rs237737241 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100535125 | AGTTCTTCACGATTA[C/T]GCTTCCCCTAGGCTC | 17973 |
rs237753084 | in-del | -/T | | | intron-variant | Nck1 | Mm_Celera | 9:100505333 | TTATTACATTATTTG[-/T]TCATTTATTTTGATA | 17973 |
rs237826395 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100522008 | CTATATAGAAAGTCC[C/T]AGGACAGCCAGGGCT | 17973 |
rs237838193 | snp | G/T | | | intron-variant | Nck1 | Mm_Celera | 9:100524990 | AGCCAATGATCTGGA[G/T]TAATAAACCCTATTC | 17973 |
rs237865655 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100524177 | GAGGCAATATACAAG[A/G]AAACTGGTTTTCCAG | 17973 |
rs237902554 | snp | C/G | | | intron-variant | Nck1 | Mm_Celera | 9:100530831 | CAACCCATATGTAAT[C/G]GGATCTGAAGTCATC | 17973 |
rs237940240 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100532072 | GTCTCAAAAGGAATA[A/G]GAAGAATATTATAGG | 17973 |
rs237940358 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100521074 | AAACCACAGAACCCA[C/T]GTAAAAAGAAAAAGC | 17973 |
rs238124591 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100506359 | CAAAATAAAACAAAC[-/A]AAAAAAAACCCTATT | 17973 |
rs238147587 | in-del | -/AAAAA | | | intron-variant | Nck1 | Mm_Celera | 9:100534271 | AATCACATAATTATT[-/AAAAA]AAAAAAAAAAAGGGA | 17973 |
rs238210514 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100523171 | TCTGCCACAGAAAGG[A/G]CCCAGCTTCTGCATG | 17973 |
rs238305709 | in-del | -/TTTTT | | | intron-variant | Nck1 | Mm_Celera | 9:100496849 | TGAGTCATTCTCTCA[-/TTTTT]TTTAAAAAAAAAAAA | 17973 |
rs238399438 | snp | C/G | | | intron-variant | Nck1 | Mm_Celera | 9:100541547 | CAACACCACCCTCAA[C/G]TACAGAGTAAGTTCA | 17973 |
rs238458881 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100542503 | TTACTGTTTTAACAC[C/T]CAGAAAAGAACATTT | 17973 |
rs238521546 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100499419 | AGATAGTAAGAAAGG[A/T]AACACATGGGGAAAT | 17973 |
rs238539207 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100514483 | ACTCCAGCTCCAGAG[A/G]ACCATACACCCTCAC | 17973 |
rs238555104 | in-del | -/AA | | | intron-variant | Nck1 | GRCm38.p3 | 9:100496853 | GTCATTCTCTCATTT[-/AA]AAAAAAAAAAAAAAG | 17973 |
rs238585077 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100508109 | GAACCAAGTCTGAAC[A/G]CCAGGCATTCTTTTC | 17973 |
rs238720958 | snp | A/C | | | intron-variant | Nck1 | GRCm38.p3 | 9:100530292 | ATGTGCCACCCCCCC[A/C]CACACACACACACAC | 17973 |
rs238748605 | snp | A/G | | | intron-variant, utr-variant-5-prime | Nck1 | Mm_Celera | 9:100507051 | AATTAAAGCTAGTAT[A/G]TTTCTAATAGTTAAA | 17973 |
rs238804315 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100530145 | CAAAGGCCAGCAAAA[C/T]GACTCAGCAGATAAA | 17973 |
rs238870153 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100541097 | AATGGCCTTGTCTGT[A/G]CTGGGAACTGAACCC | 17973 |
rs238883058 | snp | C/G | | | intron-variant | Nck1 | Mm_Celera | 9:100519235 | TTACGAAATTCCTAG[C/G]CAAATGGTTGGACCT | 17973 |
rs239004073 | snp | A/G | | | downstream-variant-500B | Nck1 | Mm_Celera | 9:100494507 | CATGTGTATCCTTGG[A/G]TTTAATATTCAATAG | 17973 |
rs239070485 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100495849 | ATATAAATGAGAAAA[A/G]TAAGGCTCAGAGAGC | 17973 |
rs239116049 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100529017 | GTTACCTAACCTTCT[-/A]GGAAATTCCCCTAGC | 17973 |
rs239198715 | snp | A/G | | | intron-variant, utr-variant-5-prime | Nck1 | Mm_Celera | 9:100545728 | AACCGCCGAGGCAGC[A/G]CGCCGCACACTTGCC | 17973 |
rs239270386 | snp | A/T | | | intron-variant | Nck1 | GRCm38.p3 | 9:100532393 | ATGCTTTGCCCTTCA[A/T]GTATGTTTGTCTATC | 17973 |
rs239293561 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100523087 | ATCTTACTTTCTATC[C/T]TCTCTGAATTAAAAT | 17973 |
rs239404245 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100542733 | CACGGAGCTACATCC[C/T]TAGCACCATCTTACA | 17973 |
rs239507942 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100516205 | GTAAGGGCAATTTAA[A/G]TTATAAACAGGCTCC | 17973 |
rs239535853 | snp | C/G | | | intron-variant | Nck1 | Mm_Celera | 9:100516409 | TCTGACCTACATAGG[C/G]ACCAAACAAGTCCAT | 17973 |
rs239590301 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100521579 | TTACTGTATGTAAAT[C/T]AACTAAGTATGGAAC | 17973 |
rs239605823 | in-del | -/CTAGATGTACCACAT | | | intron-variant | Nck1 | Mm_Celera | 9:100535771 | GACCTCCCATACAAC[-/CTAGATGTACCACAT]CTAGATGTACCACAT | 17973 |
rs239711510 | snp | C/G | | | intron-variant | Nck1 | Mm_Celera | 9:100506184 | CAAGCACACAATTAT[C/G]GCAACCATGCTACCA | 17973 |
rs239716430 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100538059 | CAACAAGACCCAGGC[A/G]CCTGGTGCACATACA | 17973 |
rs239787781 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100533036 | GAGCAGCTTCGCAGT[-/A]AAATCAGCCCTTAAT | 17973 |
rs239858911 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100541062 | CAGATCTTCAGGAAA[A/T]AGAGGGACAGACAGT | 17973 |
rs240044489 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100501503 | TCTATCCCCAGTGCC[C/T]CGCCTATATTAAATG | 17973 |
rs240292380 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100530497 | TGAGTGTGGTGGCAT[A/G]CATCTTTAACTCTCA | 17973 |
rs240322774 | snp | C/T | | | downstream-variant-500B | Nck1 | Mm_Celera | 9:100494826 | GTGAAAGGGGGTACT[C/T]GAGGTGTGGGGGACA | 17973 |
rs240359051 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100540252 | AAAACCATGTGATTA[A/G]AAGAAAACAAGTAGG | 17973 |
rs240406117 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100529574 | TGGGGACTTTTTTTT[A/T]AATGGGTAAAGAGTC | 17973 |
rs240409110 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100513381 | CCTAACCATGTCATT[C/T]GCCATGTGTTATGGT | 17973 |
rs240475107 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100528248 | TGAGCCCAGAGTGTT[C/T]CTAGGCCTGAAGGCT | 17973 |
rs240514530 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100528578 | GAAGCAGCCTCTCTT[C/T]TCTGTCTGACCTCAT | 17973 |
rs240612885 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100538320 | AGCAAATAATATTAA[C/T]AGTCATAGGATCACC | 17973 |
rs240859897 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100514342 | GACTAGAGAGAAATT[-/A]CCAAAGCTATGAGAG | 17973 |
rs240893313 | in-del | -/TTT | | | intron-variant | Nck1 | Mm_Celera | 9:100544308 | AATACAAAGGTAAGA[-/TTT]TTTTTTTTTTAAAGA | 17973 |
rs240949771 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100527454 | ATTTTTTAAAAGCTA[A/C]TAAAGAGATTAAAAA | 17973 |
rs241159175 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100515309 | TCTTACATTACATGT[A/G]GATTTAGAATTATCT | 17973 |
rs241260497 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100516366 | TCTGGGTTCTAGTCC[C/T]AGAACCCACACAGAG | 17973 |
rs241317480 | snp | A/G | | | downstream-variant-500B | Nck1 | Mm_Celera | 9:100494580 | CTGGATCAGGATGGT[A/G]AAAAGTTGAAAACCT | 17973 |
rs241389640 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100503352 | GAAATCTGCCTGCCG[A/C]GTACCTCCCAGGTTC | 17973 |
rs241462344 | in-del | -/T | | | intron-variant | Nck1 | Mm_Celera | 9:100530918 | AATAAATCGTTGTGA[-/T]TTTTGTCCCCATCCT | 17973 |
rs241468850 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100528896 | AAACAGAGCTGGTTT[C/T]TAAAAATTCTTCAAG | 17973 |
rs241476649 | in-del | -/GT | | | intron-variant | Nck1 | GRCm38.p3 | 9:100533778 | TGCGTGCGTGCGTGC[-/GT]GTGTGTGTGTACAGA | 17973 |
rs241526391 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100502717 | CATCTTGATCTAGCA[C/T]TTTAGTTTACCACAA | 17973 |
rs241577157 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100527736 | TCCTAGAGGACTTGA[A/G]TCTCTGAGTTTGAAG | 17973 |
rs241612525 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100505596 | TTAGTAACTACCTGC[C/T]CCACGAGCACAATAA | 17973 |
rs241634867 | in-del | -/T | | | intron-variant | Nck1 | Mm_Celera | 9:100498075 | ACATGATGGATCATC[-/T]TTTTGGGAAATGAAA | 17973 |
rs241656824 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100505821 | TATAACATGTACCCA[C/T]ATGCACACAGGCTTG | 17973 |
rs241685611 | in-del | -/ACACACACACACACACAC | | | intron-variant | Nck1 | Mm_Celera | 9:100525862 | TGTGGGAATTCTGTT[-/ACACACACACACACACAC]ACACACACACACACA | 17973 |
rs241724794 | snp | G/T | | | intron-variant | Nck1 | Mm_Celera | 9:100540008 | GGCAGGTAGCTGGCT[G/T]GCAAGAGAATGCCCA | 17973 |
rs241786041 | in-del | -/AA | | | intron-variant | Nck1 | GRCm38.p3 | 9:100539518 | CCTATTTCTCGATGT[-/AA]AAAAAAAAAAGCCGG | 17973 |
rs241814000 | in-del | -/AACA | | | intron-variant | Nck1 | Mm_Celera | 9:100501545 | TTTACCAGAAAAAAG[-/AACA]AACGGAGGCAAATGG | 17973 |
rs241886761 | snp | G/T | | | intron-variant | Nck1 | Mm_Celera | 9:100528686 | GGCAGAGCAGCCATG[G/T]TGCTGGATTAAAATT | 17973 |
rs241909107 | in-del | -/GACAGGCAGATCTCTGT | | | intron-variant | Nck1 | Mm_Celera | 9:100505096 | TACTTGGGAGGCAGA[-/GACAGGCAGATCTCTGT]GAGTTTGAGGCCAGT | 17973 |
rs241918604 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100507930 | CGTCAACAAAAGTGC[-/AA]AGTGACCAATCCTAT | 17973 |
rs241925714 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100535464 | TGACGTTTCAAAAGC[C/T]GTTCCCAGTTAGTTC | 17973 |
rs241964733 | snp | A/C | | | intron-variant, utr-variant-5-prime | Nck1 | Mm_Celera | 9:100506790 | TGTGTTCTCTTTTCA[A/C]AGTTTGTTGACACAG | 17973 |
rs241969433 | in-del | -/C | | | intron-variant | Nck1 | Mm_Celera | 9:100513549 | CTAAAAAAAAAAAAA[-/C]CACCAAACTAATACA | 17973 |
rs242097198 | in-del | -/A | | | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100546551 | ATGAAGCCTCGGGGG[-/A]AAAATGTAAGATGTT | 17973 |
rs242135000 | in-del | -/GTGTGTGTGTGT | | | intron-variant | Nck1 | GRCm38.p3 | 9:100513740 | TGTCAAAAAAAGAAG[-/GTGTGTGTGTGT]GTGTGTGTGTGTGTG | 17973 |
rs242350160 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100495860 | AAAAATAAGGCTCAG[A/C]GAGCATGCCTAGGAT | 17973 |
rs242643268 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100501076 | TTACATATTACCAGA[A/C]AATAAAGAATTTCTA | 17973 |
rs242660627 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100498761 | ATTTTTCCAAGATGG[C/T]ATAGTTGGCCTTCTC | 17973 |
rs242838690 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100512091 | AACTAACACACAGCC[A/G]CTTACACTTAACCTT | 17973 |
rs242927869 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100526742 | AAGTAGTGTGTATTT[A/G]TAATCTCTCGGTTCT | 17973 |
rs242993458 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100545453 | TAACACTGAACCGAC[C/T]TAGCACGGAAACCCG | 17973 |
rs243029489 | in-del | -/C | | | intron-variant | Nck1 | Mm_Celera | 9:100498805 | AAAAACAAAAAAACA[-/C]AAAAAACCCCATATA | 17973 |
rs243044279 | snp | G/T | | | intron-variant | Nck1 | Mm_Celera | 9:100536751 | TGCCTAGCATATCAG[G/T]AAGCAGTACCTCAAG | 17973 |
rs243104885 | snp | C/T | | | intron-variant | Nck1 | GRCm38.p3 | 9:100532377 | ATGCATATATATGTG[C/T]ATGCTTTGCCCTTCA | 17973 |
rs243107131 | in-del | -/TC | | | intron-variant | Nck1 | Mm_Celera | 9:100528608 | TGACAGTTGACTTAT[-/TC]TCTCTCTGACTCATT | 17973 |
rs243146722 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100522427 | TTTACAAGATTACTG[A/T]AATCAACATTTTAAG | 17973 |
rs243175661 | in-del | -/G | | | downstream-variant-500B | Nck1 | Mm_Celera | 9:100494642 | TAGAAAGGAAAAAAA[-/G]TTACATATCTCATTG | 17973 |
rs243270517 | in-del | -/G | | | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100508700 | GAACATGTTTTAAAT[-/G]GTGCTGAAGTGTAAT | 17973 |
rs243304236 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100502603 | TCAGTTATTAAGGAA[A/G]ACTGAATGAACCAAG | 17973 |
rs243304699 | snp | G/T | | | intron-variant | Nck1 | Mm_Celera | 9:100531630 | AGTACTGAGTACTTT[G/T]CCTTAATCACATTTT | 17973 |
rs243336680 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100524673 | CCAGAGTTTAGCTCC[C/T]AACACCCATATCATG | 17973 |
rs243342132 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100521450 | AACACTGGACTGCTA[C/T]AAGCACTTTGAGGAG | 17973 |
rs243354898 | in-del | -/TT | | | intron-variant | Nck1 | Mm_Celera | 9:100504559 | TTGCCCAAAAGTTGA[-/TT]TTTTTCCCAAACAGG | 17973 |
rs243504409 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100534397 | GTGACACTCTGCTGT[C/T]CTTGCAGGTCCTCTA | 17973 |
rs243566214 | snp | A/G | | | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100546551 | ATGAAGCCTCGGGGG[A/G]AAAATGTAAGATGTT | 17973 |
rs243586172 | in-del | -/CAACAACAAC | | | intron-variant | Nck1 | Mm_Celera | 9:100534724 | CAAATACAACAACAA[-/CAACAACAAC]AACAAAAAACATTAA | 17973 |
rs243624083 | snp | C/G | | | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100547654 | GCAAGTTCAAGGCCA[C/G]CCTGGTTTATGTAGC | 17973 |
rs243656635 | in-del | -/C | | | intron-variant | Nck1 | Mm_Celera | 9:100534718 | GCATAGCAAATACAA[-/C]AACAACAACAACAAC | 17973 |
rs243827033 | in-del | -/TTT | | | downstream-variant-500B | Nck1 | Mm_Celera | 9:100494540 | CGAAAAATGTTGTTG[-/TTT]TTTTCCAGTAAATCT | 17973 |
rs243829972 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100540112 | TCTCAAAAATAAATA[A/T]ATATATAAATAAACA | 17973 |
rs243874727 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100510887 | AGTGAGGGGACGCTA[C/T]TTGTATTACTGCAAC | 17973 |
rs243894479 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100529244 | TAACAAAGGACACAG[C/T]CACAAAAAGACAGTA | 17973 |
rs243992340 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100508761 | TAAACATTTAAGAGG[C/T]CAGGAATTATGACTC | 17973 |
rs244226320 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100538103 | ACACTCACACATGTG[-/A]AAAAAAATTCAGGAA | 17973 |
rs244255909 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100529716 | GACTAATAAGATCTC[A/G]TCTTAAAAAAGAAAA | 17973 |
rs244255968 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100516256 | GTTTCTTAACTTGGC[A/G]TAGAACATAACTAAA | 17973 |
rs244289307 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100516787 | TCTACCAATTCTGTA[C/T]CATTAAAATCTCAGA | 17973 |
rs244291235 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100504014 | GTTATTCTTTCTCAG[A/G]CAAATCTTTGTACTA | 17973 |
rs244299966 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100502595 | CTATAGTCTCAGTTA[C/T]TAAGGAAAACTGAAT | 17973 |
rs244363766 | snp | G/T | | | intron-variant | Nck1 | Mm_Celera | 9:100514301 | ATAAAATTCTTAGAA[G/T]GATATGTTACAGAAC | 17973 |
rs244380728 | in-del | -/T | | | intron-variant | Nck1 | Mm_Celera | 9:100500566 | ACAAAAGGAAACAGA[-/T]TAAGAAAACAGCACA | 17973 |
rs244427325 | in-del | -/ATCAAC | | | intron-variant | Nck1 | Mm_Celera | 9:100527201 | CATTTCCATTTTCAA[-/ATCAAC]ATCAGAAGCCATTGC | 17973 |
rs244570600 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100515349 | GTTCAAACATAAAAC[A/G]AAAATTAGCACATTT | 17973 |
rs244594864 | in-del | -/CATG | | | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100507378 | TGGTCTGTCAAATGC[-/CATG]CATGATAACTGCAGA | 17973 |
rs244642381 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100508050 | TTAGCGTGTCAAAAA[A/G]GTTCAATAATGTGCC | 17973 |
rs244654949 | in-del | -/ACA | | | intron-variant | Nck1 | Mm_Celera | 9:100534713 | GTTTGCATAGCAAAT[-/ACA]ACAACAACAACAACA | 17973 |
rs244730277 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100543221 | ATTAAAAAGCAAGGG[A/G]AAAAAAAAAGTCAGC | 17973 |
rs244744457 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100505824 | AACATGTACCCACAT[A/G]CACACAGGCTTGTAC | 17973 |
rs244751148 | snp | G/T | | | intron-variant | Nck1 | Mm_Celera | 9:100497205 | TCAACCTTTCCAACC[G/T]TATTTATTAATGCAT | 17973 |
rs244832107 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100542217 | TACCTAGTAAGTTTC[A/G]GCTCAACCAGGGCTA | 17973 |
rs244950835 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100520900 | CTATGTACAAACACA[A/G]CAATAAACAGCTAAC | 17973 |
rs245002600 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100510102 | ATACTGCAAACAGTC[A/T]AAGGGAATAGTAACA | 17973 |
rs245060034 | snp | G/T | | | intron-variant | Nck1 | Mm_Celera | 9:100504213 | CCACCATGGAGTTCT[G/T]CACCAACACAACCAC | 17973 |
rs245090940 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100526715 | AATAAATAAAAATTT[-/A]AAAAAAGGACAAAGT | 17973 |
rs245181286 | in-del | -/AG | | | intron-variant | Nck1 | Mm_Celera | 9:100536067 | CTTAACAAAATTGGC[-/AG]AGACTACTAACCTAC | 17973 |
rs245201657 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100544590 | CATTTGATTTTCTGG[C/T]ATTGAAAGCATCCAT | 17973 |
rs245278729 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100534047 | ACCACCCCCCCCCAA[A/C]AAAAAAAAGAGTCCA | 17973 |
rs245345287 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100543882 | CCCAAAACTGAGGGA[A/C]GGCAAAAGAGACAGG | 17973 |
rs245406037 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100531523 | CTAGGATTCCTGGCA[A/G]GAATAACCACATCCT | 17973 |
rs245410729 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100498576 | CCCCTGTGAGCCTTG[C/T]TGTAACAATGTCTTA | 17973 |
rs245491606 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100541032 | AAGTATACATAATGG[A/G]GTGCCCAAGGAGGTC | 17973 |
rs245516464 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100514870 | CACTTCAAGGGCCCA[A/T]CACTTCCCAACAGCA | 17973 |
rs245567265 | in-del | -/GAAAAA | | | intron-variant | Nck1 | GRCm38.p3 | 9:100542058 | ACCAAAACATATCTG[-/GAAAAA]AAAAAAAAAAAAAGC | 17973 |
rs245775632 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100536341 | ATGGAAGAGCTAGGG[A/G]AAGGATGGAAGGAGC | 17973 |
rs245846070 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100523472 | TATTAGTTAAAGAGT[A/T]ATTACCCTAATCCTT | 17973 |
rs245894769 | snp | A/T | | | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100546289 | GCCCTGAGTGGTCCC[A/T]GAGCTGAGACTGCGC | 17973 |
rs245896208 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100535130 | TTCACGATTACGCTT[C/T]CCCTAGGCTCTCTAG | 17973 |
rs246145690 | snp | C/G | | | intron-variant | Nck1 | Mm_Celera | 9:100535366 | GCCATATATTTGAAT[C/G]TTTGGTTACCACTCA | 17973 |
rs246178165 | in-del | -/AAAAAAAAA | | | intron-variant | Nck1 | Mm_Celera | 9:100510388 | GCATTATTTTAAAAT[-/AAAAAAAAA]ATATATATATATATA | 17973 |
rs246231888 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100528457 | CTCAAACTCCTTTCT[A/G]AGCTAACTGATTCAA | 17973 |
rs246303351 | in-del | -/C | | | intron-variant | Nck1 | Mm_Celera | 9:100528549 | TGAACTACACTCTCT[-/C]CCCGTGCTGCTCTGA | 17973 |
rs246364184 | in-del | -/T | | | intron-variant | Nck1 | Mm_Celera | 9:100503928 | AGGCAGATTTCTGAA[-/T]GTGAGGCCAAGCTGT | 17973 |
rs246438105 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100539639 | GTTTCAGGACAGCCA[A/G]GGCTATACAGAGAAA | 17973 |
rs246464094 | in-del | -/AAAG | | | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100547773 | GATATTTGGGGTAAT[-/AAAG]AAAGGAAATAAGAAT | 17973 |
rs246540892 | snp | G/T | | | intron-variant | Nck1 | Mm_Celera | 9:100536526 | CCCTATCTGGCATCA[G/T]GAGGAGAAGAAGTCC | 17973 |
rs246596769 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100526239 | CTAAGCCTCTGTACA[C/T]ACCACTACACATCTA | 17973 |
rs246621353 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100537247 | CTTCTAAGAAATGAA[A/G]AAATTCATCAGATAA | 17973 |
rs246839230 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100518374 | AAGAATGCGAATCGA[C/T]CCATACTTATCTCCT | 17973 |
rs246845495 | in-del | -/CACA | | | intron-variant | Nck1 | Mm_Celera | 9:100521239 | ACAGCTTCTGAGGAG[-/CACA]CACACACACAAACAC | 17973 |
rs246858016 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100505130 | GTTTGAGGCCAGTGA[A/G]TTCTAAGATATCCAG | 17973 |
rs246870492 | in-del | -/AGAT | | | intron-variant | Nck1 | Mm_Celera | 9:100511350 | AGGGATATTTTTCAA[-/AGAT]AGGCTAAAGAACTAT | 17973 |
rs246876259 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100503085 | TTATTATCATGACAC[A/C]GTTGGACCAACCTGG | 17973 |
rs246877821 | in-del | -/TC | | | intron-variant | Nck1 | Mm_Celera | 9:100509787 | CTTCTCTCCTCTTTA[-/TC]TCTCTCTTTCTCTCT | 17973 |
rs246917373 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100528521 | TGCTTGGAAAAAATG[C/T]CCCTGAACTCCATGA | 17973 |
rs246945442 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100539171 | GATCCCAGCACTTTG[A/G]AACAGAGGCAGGCCG | 17973 |
rs246991107 | in-del | -/GAGAGGATTAT | | | intron-variant | Nck1 | Mm_Celera | 9:100523316 | ATTCTGGAATCTGAA[-/GAGAGGATTAT]GTTTTATAATAACTA | 17973 |
rs247164832 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100523650 | CAATCATCATCACCA[C/T]ATAAAACCAGATGTA | 17973 |
rs247224793 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100516812 | CTCAGAAAATTAAAT[C/T]CTAAGAAATAATTAA | 17973 |
rs247236468 | in-del | -/ATAAA | | | intron-variant | Nck1 | Mm_Celera | 9:100532345 | TTTTATTTTATTTAC[-/ATAAA]ATAAATTCCAGCATG | 17973 |
rs247374173 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100502319 | ATTTGTTTCTCATAG[C/T]TCTGGAAGCTGGAAG | 17973 |
rs247434761 | in-del | -/A | | | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100508754 | CATGCTTAAACATTT[-/A]AAGAGGCCAGGAATT | 17973 |
rs247521450 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100516696 | TATATATCTAGGGAA[C/T]TTTAAAGAAAGATGT | 17973 |
rs247528042 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100511915 | AGGACCCTGGAGTTA[A/G]TAACAGGAAGATTGT | 17973 |
rs247578873 | snp | A/G | | | downstream-variant-500B | Nck1 | GRCm38.p3 | 9:100494642 | TAGAAAGGAAAAAAA[A/G]TTACATATCTCATTG | 17973 |
rs247606532 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100500918 | AAACTGTATATGGAG[C/T]GGACATACAGCGTAA | 17973 |
rs247607606 | in-del | -/AAAA | | | intron-variant | Nck1 | GRCm38.p3 | 9:100520006 | GAAAGAACTACCTTC[-/AAAA]AAAAAAAAAAAGATA | 17973 |
rs247818619 | in-del | -/AG | | | intron-variant | Nck1 | Mm_Celera | 9:100529531 | AAAAAAAAAAAAAAA[-/AG]AAAGTAGTTGCTAGG | 17973 |
rs247829940 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100504452 | ACGTCTTCAAACCTG[C/T]TTCTCCCTTGTGGAC | 17973 |
rs247851237 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100521473 | TTGAGGAGAGATTTT[C/T]TTTTAATTAGACCCC | 17973 |
rs247916923 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100544054 | CTTGCAGAGGATCTC[C/T]GTTCTGTCCCCAGAG | 17973 |
rs247981761 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100537920 | TGGAGCTAGAGAGAC[A/G]TCTCAGCAGGTAAGG | 17973 |
rs248044177 | in-del | -/CC | | | intron-variant | Nck1 | Mm_Celera | 9:100529809 | CACAACACCAGGAGG[-/CC]CCAACAATCCAAGTG | 17973 |
rs248076984 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100544799 | AATACACGGATCTGT[A/T]GGGCTTGGAAACCTA | 17973 |
rs248101201 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100528788 | GCTCCTTAGAGGAAG[A/T]TGTTGTTGACCAGTG | 17973 |
rs248103714 | snp | G/T | | | intron-variant | Nck1 | Mm_Celera | 9:100519416 | ccaaagtgtggacac[G/T]ttgctcattcttaga | 17973 |
rs248273169 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100525308 | ACAATGAACTTATTA[C/T]TTTTGTGGTCCTTAA | 17973 |
rs248274437 | in-del | -/AAAAA | | | intron-variant | Nck1 | Mm_Celera | 9:100520005 | GAAAGAACTACCTTC[-/AAAAA]AAAAAAAAAAAAAAA | 17973 |
rs248340141 | snp | A/C | | | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100508382 | AAAGCCAAAACTAAG[A/C]TCTAAAATGAAAGCT | 17973 |
rs248509684 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100511709 | AAAGGAAAAGAGCCT[C/T]CAGAGAAAAGGTGAA | 17973 |
rs248510097 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100533753 | GGAGAAAATACAAGG[A/G]TGTCTATGCGTGCGT | 17973 |
rs248511473 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100500169 | ACACATACCAACACC[A/T]CCAACAATTAAAGAA | 17973 |
rs248620498 | in-del | -/AAAA | | | intron-variant | Nck1 | Mm_Celera | 9:100535929 | AACTAATTAGAGCTG[-/AAAA]AAAAAAAAAAAAAAA | 17973 |
rs248654521 | snp | G/T | | | intron-variant | Nck1 | Mm_Celera | 9:100529039 | TCCCCTAGCCCTGCA[G/T]GAAGGGGAGCCTGCT | 17973 |
rs248693455 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100543489 | ATCCAAGGCTGATTC[A/C]CTACAACAGGAGGCT | 17973 |
rs248812352 | snp | A/G | | | synonymous-codon | Nck1 | Mm_Celera | 9:100497795 | GCATTTCTCCATGAC[A/G]ATCACCTTGGTCCCT | 17973 |
rs248877048 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100535889 | ACTGCCTAAGCTCAG[C/T]CCCAAGACATCTATA | 17973 |
rs248950648 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100533810 | AGATAGGTGTGTAGA[A/C]ATGCATTCACTGTCT | 17973 |
rs249020107 | in-del | -/AAC | | | intron-variant | Nck1 | Mm_Celera | 9:100513547 | CACTAAAAAAAAAAA[-/AAC]CACCAAACTAATACA | 17973 |
rs249031266 | snp | A/G/T | | | intron-variant | Nck1 | GRCm38.p3 | 9:100524837 | GACTTATTAATTACA[A/G/T]GTATAGGGAACTGGT | 17973 |
rs249064763 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100544349 | AAAAAAACAGTACAA[C/T]GTTAAGGTTTATGTC | 17973 |
rs249131907 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100520040 | TGCTTTCCCCCACAA[C/T]GGTAATTCATTGGTT | 17973 |
rs249136971 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100523975 | CCAGTATGACTGGTG[C/T]TCCTGTAAGAGAAGT | 17973 |
rs249173007 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100534860 | AAGCAGCTAGGATTA[A/C]AGGCAAGGACTTTAT | 17973 |
rs249224114 | snp | A/G | | | intron-variant | Nck1 | GRCm38.p3 | 9:100501650 | GGCATGATGGAATGG[A/G]GACCCGGCATGATGG | 17973 |
rs249256247 | snp | C/G | | | intron-variant | Nck1 | Mm_Celera | 9:100524106 | CCTCAGACTTACTAT[C/G]TCACCAAGGCTCAAG | 17973 |
rs249263740 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100516466 | ATACCCATACACATT[A/T]AAAACATTTTTTCAA | 17973 |
rs249264054 | in-del | -/T | | | intron-variant | Nck1 | Mm_Celera | 9:100524706 | GCTAACATTTGCCTA[-/T]TAACATCAGCTCCAA | 17973 |
rs249326357 | in-del | -/TT | | | intron-variant | Nck1 | Mm_Celera | 9:100521917 | TGTCAAGACAGTCAC[-/TT]GTGATCTCAAATGCC | 17973 |
rs249504487 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100500107 | AACATACATAGGAGT[A/G]ACACTATACAGAATG | 17973 |
rs249605485 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100527934 | GGTGTGGTGGCTCAC[A/G]TCTTTAATCCCAGCA | 17973 |
rs249630043 | snp | A/T | | | downstream-variant-500B | Nck1 | Mm_Celera | 9:100494871 | GTATTTTTGTTTAAA[A/T]TGGCTATAAATTATG | 17973 |
rs249730853 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100496873 | AAAAAAAAAAAGAGG[A/G]AGATTTTAATCAAAC | 17973 |
rs249795146 | snp | G/T | | | intron-variant, utr-variant-5-prime | Nck1 | Mm_Celera | 9:100545656 | GCGCCCTTCCTGCCA[G/T]CCTACCGTCCCGGCC | 17973 |
rs249867675 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100498299 | TTTATTGACCAAGAT[A/T]TTGTAACGAGCTGTA | 17973 |
rs249876246 | snp | G/T | | | intron-variant | Nck1 | Mm_Celera | 9:100503246 | TTTTATGTATGTTTG[G/T]GGGGGAGGGAGAGGG | 17973 |
rs249982330 | snp | C/G | | | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100507855 | GGCTCCCCCCATCTG[C/G]CTTACTTAATAAAGG | 17973 |
rs250003794 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100535085 | CAAAGCAAGAGCAAT[-/A]AGGATTTATTATATT | 17973 |
rs250150019 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100508885 | TAAGCTACAGAGTAA[A/G]ACCCTGTCTCAAAAC | 17973 |
rs250217357 | snp | C/T | | | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100548020 | TAGGAAAGAGTCTAC[C/T]TTGTATGGAAGGTGC | 17973 |
rs250259393 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100542003 | TTCTAGGATTTGGCA[A/G]TTTATTTTAAACAAA | 17973 |
rs250281131 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100540388 | GAGGTGAGAATACAT[C/T]ATGGAAAAAAGACAT | 17973 |
rs250325637 | in-del | -/TTTTG | | | intron-variant | Nck1 | GRCm38.p3 | 9:100500793 | GTTTTTTTTTTTTTT[-/TTTTG]TACTGAGTTTTTTGT | 17973 |
rs250331159 | in-del | -/ATGT | | | intron-variant | Nck1 | Mm_Celera | 9:100528414 | CTCTCTGAACCCTGG[-/ATGT]CTGTCTGGTTCAAAT | 17973 |
rs250379306 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100501436 | TACAGTTTTTTTTTT[A/T]ATTTTCACCTTAATG | 17973 |
rs250445885 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100511514 | TTTGCTGACAAACTA[C/T]ATATTCCAGAATTTA | 17973 |
rs250604242 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100496158 | AACTCACTCTGTATA[C/T]CAGGCTGGCCTCGAA | 17973 |
rs250680958 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100503764 | CCTCTGGAAGAGTAG[C/T]CAGTGGTCTCATCCA | 17973 |
rs250792509 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100505457 | TCATATGGGTTGTCC[A/G]GCTTGATGACAAGTG | 17973 |
rs250816575 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100511224 | GTAGTTGTCAACTCA[A/G]CCTCTGACATACAGA | 17973 |
rs250855654 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100502935 | ATTGATATGTATAAA[A/C]CTATATTACAAAGTT | 17973 |
rs250858170 | in-del | -/TC | | | intron-variant | Nck1 | Mm_Celera | 9:100525661 | TTAAAGAATTCATAT[-/TC]TCTCTCTCTCTCTCT | 17973 |
rs250863687 | in-del | -/C | | | intron-variant | Nck1 | Mm_Celera | 9:100509755 | AACCCATTTTAACAA[-/C]CCCTTGTAACTCCAT | 17973 |
rs250890611 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100542135 | GCCTGGTAAAGTACA[A/C]CTTCAAACCCAGTAC | 17973 |
rs250946718 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100523119 | AATTTACCCAAGATT[A/G]CATCCTCTCGGGCTG | 17973 |
rs250977639 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100539147 | TAACTCTGCTAGGCA[C/T]ACACTTTCGATCCCA | 17973 |
rs251096732 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100522979 | AAAAGGAATTCTAGT[A/G]AAACTCCTGTTTCTT | 17973 |
rs251223875 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100528951 | ACATAGCAGCCAATC[-/A]AAAATGCACTAATGT | 17973 |
rs251310637 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100524229 | TGAATTCATGGCAGT[C/T]GTAACAACACGCACA | 17973 |
rs251343389 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100538438 | CATCCATCAACACAA[A/G]TAAGAGTTACATATA | 17973 |
rs251400563 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100528283 | GTTTCCATACTCTCT[A/C]ATCTTCTGCAGCTCT | 17973 |
rs251437934 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100528902 | AGCTGGTTTCTAAAA[A/C]TTCTTCAAGGTATCA | 17973 |
rs251475851 | snp | A/T | | | intron-variant | Nck1 | Mm_Celera | 9:100544999 | CCAACGCATACGCTT[A/T]GACTTAACTATCACG | 17973 |
rs251559695 | snp | C/G | | | intron-variant | Nck1 | Mm_Celera | 9:100529992 | AATGTTGACCACCAG[C/G]GGATCAAACACTGGG | 17973 |
rs251576411 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100539978 | ATTCAACCTCAAATA[C/T]TACAATTAAAAGTGG | 17973 |
rs251578973 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100528541 | GAACTCCATGAACTA[A/C]ACTCTCTCCCCGTGC | 17973 |
rs251654792 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100512479 | CAGGCCTAATCAGAC[A/G]AGTCAGTTAAGAAAC | 17973 |
rs251679424 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100540761 | GCTGAAGAAATAATC[A/G]GCACTCACACTTATC | 17973 |
rs251789322 | in-del | -/AAA | | | intron-variant | Nck1 | Mm_Celera | 9:100529303 | AAATTTATTGAAAGG[-/AAA]AAAAAAAAACAGATT | 17973 |
rs251815048 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100545333 | TCTTTCCTAACTAAG[-/A]GGCAGTATTTTTCTT | 17973 |
rs251857575 | snp | C/G | | | intron-variant, utr-variant-5-prime | Nck1 | Mm_Celera | 9:100545896 | CGGGCCAACTTCGCC[C/G]GGGAAAGAGGAAGCG | 17973 |
rs251927677 | snp | G/T | | | intron-variant | Nck1 | Mm_Celera | 9:100544431 | AGGCGTGGGGCATCA[G/T]TTGTGAAGGGAAGAC | 17973 |
rs251945201 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100535005 | AGGTATATTCCACTG[C/T]CCTAAGCTCCTTTTC | 17973 |
rs252041617 | in-del | -/A | | | intron-variant | Nck1 | Mm_Celera | 9:100525070 | AAGTGAATGTACAGT[-/A]ACAGCATTCTGGCCA | 17973 |
rs252094495 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100516307 | TTCAAAGTAAGGGCT[A/G]GAGGGATAGCTCATC | 17973 |
rs252125630 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100504416 | CCCTGAATTATCATC[C/T]CACTCTGTTCTTCTG | 17973 |
rs252151576 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100516065 | CCCTACAGAGACTAC[C/T]TAAAATACATTTTCA | 17973 |
rs252200683 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100514745 | GAAGGAACAGAGCCA[C/T]TTATTTTATGGTTAA | 17973 |
rs252255502 | in-del | -/GTT | | | intron-variant | Nck1 | Mm_Celera | 9:100496735 | AATGGTGTTAAGCAG[-/GTT]GTTGAGGTGAATAAT | 17973 |
rs252308834 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100521357 | CTGTACCTCAGATAA[C/T]GAATGGTCTGAAGCA | 17973 |
rs252469048 | snp | C/G | | | intron-variant | Nck1 | Mm_Celera | 9:100498860 | TTTTCAGATTTACTT[C/G]AAGATTTAAACCCTT | 17973 |
rs252501854 | in-del | -/AGAAAGAA | | | intron-variant | Nck1 | GRCm38.p3 | 9:100536888 | TCAGACTTAAGCCAC[-/AGAAAGAA]AGAAAGAAAGAAAGA | 17973 |
rs252519102 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100525118 | GCAGCTTACTAAGAT[A/G]ATGAAGCATCCTTTA | 17973 |
rs252558928 | in-del | -/AAAAG | | | intron-variant | Nck1 | Mm_Celera | 9:100516728 | TCTCTATTAAAAAAA[-/AAAAG]AAAAGAAAAGAAAAG | 17973 |
rs252605453 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100524240 | CAGTCGTAACAACAC[A/G]CACAAGATCTGCACA | 17973 |
rs252606484 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100535268 | AAGTACTTTTGAAGT[A/G]TAGCGGGAATATGAA | 17973 |
rs252625327 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100511015 | CCTGCTATGCAAACC[A/G]GGGGAAGAATTTGAT | 17973 |
rs252709162 | in-del | -/C | | | intron-variant, upstream-variant-2KB | Nck1 | GRCm38.p3 | 9:100507843 | AGAGAGAAGTAGGCT[-/C]CCCCCCATCTGCCTT | 17973 |
rs252771031 | in-del | -/TTAAGCC | | | intron-variant | Nck1 | Mm_Celera | 9:100530120 | TAGCTAAACAAGTAA[-/TTAAGCC]TTAAGCCTTCAAAGG | 17973 |
rs252812461 | in-del | -/CTACACTTCCTCCTTTT | | | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100507091 | TACATTCTTCATTTC[-/CTACACTTCCTCCTTTT]CCTTGACTTCCAAAC | 17973 |
rs252836202 | snp | C/G | | | intron-variant, utr-variant-5-prime | Nck1 | Mm_Celera | 9:100545627 | CTTCCTCAGGCTGGC[C/G]GCTGGAGGTGAGAGC | 17973 |
rs252877639 | snp | C/T | | | downstream-variant-500B | Nck1 | Mm_Celera | 9:100494603 | GAAAACCTTAAATTA[C/T]TGACATGAGGAATTA | 17973 |
rs252891616 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100542185 | GGATGTTTTGTGAAT[C/T]TGAGGCCAGCCTGGT | 17973 |
rs252894499 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100536887 | gtcagacTTAAGCCA[A/C]agaaagaaagaaaga | 17973 |
rs252918426 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100495828 | TCCTCAAAATAAACC[C/T]TTTTTATATAAATGA | 17973 |
rs253059451 | in-del | -/TGTT | | | intron-variant | Nck1 | Mm_Celera | 9:100512354 | AACCTTCTTTAGCAC[-/TGTT]TGTTTATTTAATAAA | 17973 |
rs253203143 | in-del | -/C | | | intron-variant | Nck1 | Mm_Celera | 9:100496373 | ATAAGAAAATGGACT[-/C]CCATTATCTTGTCTG | 17973 |
rs253223041 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100500757 | ATCTTGTACTTCACA[A/G]ATAACTGTATAATAG | 17973 |
rs253277529 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100533960 | CAGGCGGATTTCTGA[A/G]TTCAAGGCCAGCCTG | 17973 |
rs253313239 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100500133 | GAATGAGCAGATTGT[A/G]TTAAATATTTAAGAA | 17973 |
rs253401005 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100498533 | CCCCTCTTACCGTGA[C/T]ATTTGCTCACTCCTG | 17973 |
rs253626116 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100514150 | ATATCCTTTAACAAA[C/T]GACTGCCTTAAAAAA | 17973 |
rs253652252 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100537658 | TCCACAGACAAACAC[A/G]TACACATGAATAAAT | 17973 |
rs253699972 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100501860 | GGCATGATGGAATGG[A/G]GATCCGGCATGATGG | 17973 |
rs253777459 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100536728 | ATATAGCTCAGTGGC[A/G]GGACACTTGCCTAGC | 17973 |
rs253848803 | snp | A/G | | | intron-variant, utr-variant-5-prime | Nck1 | Mm_Celera | 9:100545745 | GCCGCACACTTGCCT[A/G]CCCGCCTCCCCGACC | 17973 |
rs253872282 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100496124 | ACAGGGTTTCTCTGT[A/G]CAGCCCTGGCTGTCC | 17973 |
rs253925788 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100524337 | TATTGGTAAATGACA[A/G]CTACCAGGAAAGGGT | 17973 |
rs253940286 | in-del | -/CCGGCATGC | | | intron-variant | Nck1 | Mm_Celera | 9:100540697 | GAACTATGGTATGAT[-/CCGGCATGC]CTACTTCTAGGAATA | 17973 |
rs253961833 | in-del | -/AAAAAAAAAAAAAAA | | | intron-variant, upstream-variant-2KB | Nck1 | Mm_Celera | 9:100508346 | AAAATAAATAAATCT[-/AAAAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 17973 |
rs254001250 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100510427 | CACTGTCCTGAAACG[C/T]AAGTTTAGACTTGAT | 17973 |
rs254070265 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100523680 | AGTAGCACATGCCTG[C/T]AGTTCCAGAACTGGG | 17973 |
rs254145883 | in-del | -/AG | | | intron-variant | Nck1 | Mm_Celera | 9:100530348 | CACACACACACACAC[-/AG]AGATATGCACACAAT | 17973 |
rs254177667 | in-del | -/CACA | | | intron-variant | Nck1 | Mm_Celera | 9:100530334 | ACACACACTCATGAG[-/CACA]CACACACACACAGAT | 17973 |
rs254213276 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100504337 | ACTAGCTTTCTTTCA[C/T]TTAATCACTAAGTAA | 17973 |
rs254247640 | in-del | -/T | | | intron-variant | Nck1 | Mm_Celera | 9:100509264 | AAGTACAAAATTAAA[-/T]ATATATTGGTATAAC | 17973 |
rs254274040 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100502764 | TTGGTTTTTTTTCCC[C/T]AAATTATTTTATTCC | 17973 |
rs254285627 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100514237 | TAAGGGAATTACAGG[A/G]AGTGGAAAAAAGCCA | 17973 |
rs254287138 | snp | C/G | | | intron-variant | Nck1 | Mm_Celera | 9:100528582 | CAGCCTCTCTTTTCT[C/G]TCTGACCTCATGACA | 17973 |
rs254449765 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100528260 | GTTCCTAGGCCTGAA[A/G]GCTTCTAGTTTCCAT | 17973 |
rs254459200 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100528378 | CAAGACTTACTGCTG[A/G]ATAAACTCTCTCTTT | 17973 |
rs254473317 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100543036 | GTATCATAAAGAACA[C/T]ATGACACTTGAATAA | 17973 |
rs254503313 | snp | C/G | | | intron-variant | Nck1 | Mm_Celera | 9:100543311 | AAAACACACCGCTCT[C/G]TGCGCTAACTTAAAA | 17973 |
rs254539449 | in-del | -/GGG | | | intron-variant | Nck1 | Mm_Celera | 9:100522181 | CTAGTGGCGGAGGAA[-/GGG]GGGGGGGGACATCTA | 17973 |
rs254551452 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100532538 | TATTTAATCTTGAAC[A/C]ATCTCTGCAGCCCTG | 17973 |
rs254587450 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100527623 | GAAGAAAAATAAAAA[C/T]GTATATTCATACTGT | 17973 |
rs254722282 | snp | A/G | | | intron-variant | Nck1 | Mm_Celera | 9:100510541 | TGGGTATTGACTACC[A/G]TGTCAGTTTTCTCAA | 17973 |
rs254748098 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100530293 | TGTGCCACCCCCCCA[A/C]ACACACACACACACA | 17973 |
rs254899306 | snp | C/G | | | intron-variant | Nck1 | Mm_Celera | 9:100500664 | AGTCCCTCTTCATCA[C/G]TGATAGTATACCTAG | 17973 |
rs254902816 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100532951 | AAATACAGTGTACTA[C/T]TGACAACCAGGGTCC | 17973 |
rs255054477 | in-del | -/GCGT | | | intron-variant | Nck1 | GRCm38.p3 | 9:100533770 | TCTATGCGTGCGTGC[-/GCGT]GTGCGTGCGTGTGTG | 17973 |
rs255086438 | snp | C/T | | | intron-variant | Nck1 | Mm_Celera | 9:100496005 | GACTTTCACTCCATC[C/T]CCTATCAGTTCAGAG | 17973 |
rs255098375 | snp | A/C | | | intron-variant | Nck1 | Mm_Celera | 9:100541284 | AAATGTTTCCAATCC[A/C]CTGTTTATGTTTCTG | 17973 |
rs255110004 | in-del | -/AAA | | | intron-variant | Nck1 | Mm_Celera | 9:100533154 | CAGGGACTTTTTTTT[-/AAA]AAAGGAATATATGCA | 17973 |
rs255218801 | in-del | -/AC | | | intron-variant | Nck1 | Mm_Celera | 9:100506360 | AAATAAAACAAACAA[-/AC]AAAAAAACCCTATTA | 17973 |
rs255301789 | in-del | -/TATATATT | | | upstream-variant-2KB | Nck1 | Mm_Celera | 9:100547616 | ATATATATATATATA[-/TATATATT]TGCAGAGACAGGTTC | 17973 |