SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6222436 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nup37 | Mm_Celera | 10:88157808 | GACGAGCATCTTGAC[A/G]AAAGACTGAGAGTTG | 69736 |
rs29314286 | snp | G/T | 0.5 | 0 | intron-variant | Nup37 | Mm_Celera | 10:88160135 | CAGGAAAACTCTTCC[G/T]AATTGATAAAGTTAG | 69736 |
rs29316790 | snp | C/T | 0.475309 | 0.108333 | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88148635 | CAACATAACTGAGCA[C/T]ACATGTATTTCTATG | 69736 |
rs29318225 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Nup37 | Mm_Celera | 10:88172847 | TTCCTTTTTTTTGTT[G/T]TTGTTGTTCTAGCTT | 69736 |
rs29319385 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Nup37 | Mm_Celera | 10:88171180 | GCTGTGCTCCTCAGC[A/G]TTGAATGTGTTCACT | 69736 |
rs29320280 | snp | A/G | 0.493827 | 0.0552116 | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88148399 | GTCCACAAACTATAC[A/G]GAGTGACAGTAGAGA | 69736 |
rs29320855 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nup37 | Mm_Celera | 10:88149633 | AGGGAAATGAGAAGA[A/G]CGTTTGTATCATTCA | 69736 |
rs29324076 | snp | C/G | 0.465374 | 0.126941 | intron-variant | Nup37 | Mm_Celera | 10:88149921 | CTGAGTTTCCTCACT[C/G]TGCCCTTGGAGATCC | 69736 |
rs29325885 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Nup37 | Mm_Celera | 10:88149414 | AATGTGGACCACTTA[C/T]GTGTTGAAAACGCAA | 69736 |
rs29331720 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Nup37 | Mm_Celera | 10:88153712 | ATCCATGCCTATTGT[C/T]GGTCACCTTAGATGA | 69736 |
rs29332073 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Nup37 | Mm_Celera | 10:88172844 | ATTTTCCTTTTTTTT[G/T]TTGTTGTTGTTCTAG | 69736 |
rs29334536 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nup37 | Mm_Celera | 10:88157071 | TTCCAGGACAGCCAC[A/G]GCTATACAGAGAAAC | 69736 |
rs29336317 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Nup37 | Mm_Celera | 10:88148987 | TAAGAGTGGAGATTC[A/G]GGAAACCTAATTTGG | 69736 |
rs29343049 | snp | C/T | 0.345679 | 0.230967 | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88148559 | TATATAGATGATAGA[C/T]GTAAAAACAATGAAG | 69736 |
rs29346286 | snp | A/G | 0.487535 | 0.077957 | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146408 | ACCCCTGCATTAGCT[A/G]TACCTCGTGATTACC | 69736 |
rs29347111 | snp | A/G | 0.5 | 0 | intron-variant | Nup37 | Mm_Celera | 10:88154788 | TTCAGCACTATACCC[A/G]ACACGTTCACGTGGG | 69736 |
rs29347834 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nup37 | Mm_Celera | 10:88177009 | CTTTTGCACAGGAGT[A/G]GCCTGTCTTAGACCG | 69736 |
rs29348248 | snp | A/G | 0.290657 | 0.246672 | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88148753 | TTCCTAGCTTTCATA[A/G]ATAATGTTCAGCTTT | 69736 |
rs29350568 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Nup37 | Mm_Celera | 10:88161568 | TCTATACAGCTTCTA[A/G]CTATTTAGTGCCTCA | 69736 |
rs29351335 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nup37 | Mm_Celera | 10:88149634 | GGGAAATGAGAAGAG[C/T]GTTTGTATCATTCAA | 69736 |
rs29351902 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Nup37 | Mm_Celera | 10:88155988 | CCTCCCCCCAACACA[C/G]AAAGGGTTAATGTGG | 69736 |
rs29352879 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Nup37 | Mm_Celera | 10:88150036 | GAAAAACACCAGTCT[C/T]CACTGTAGGGTCATC | 69736 |
rs29356281 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Nup37 | Mm_Celera | 10:88149095 | TTGTGGTTAGTATGA[A/G]CAGCAGTGGCAGTTA | 69736 |
rs29356572 | snp | A/T | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145226 | GGAATCAATAACTTA[A/T]CCAGCCCAAACTGCC | 69736 |
rs29363891 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Nup37 | Mm_Celera | 10:88170717 | TAGTGATAAGAATTA[C/T]GCTAGCCCAATACTT | 69736 |
rs29364075 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nup37 | Mm_Celera | 10:88149635 | GGAAATGAGAAGAGC[A/G]TTTGTATCATTCAAA | 69736 |
rs29366710 | snp | C/G | 0.359862 | 0.224567 | intron-variant | Nup37 | Mm_Celera | 10:88161623 | TCCTTGCATCTTTTT[C/G]TCTTTATACAATTTA | 69736 |
rs29367950 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Nup37 | Mm_Celera | 10:88150956 | AAAGGTTATCGTAGA[C/T]TTTGTCTTATGTTGA | 69736 |
rs29371996 | snp | A/G | 0.5 | 0 | intron-variant | Nup37 | Mm_Celera | 10:88158193 | GCCAAAATGTTGGAT[A/G]TCCTGATTTAAATAT | 69736 |
rs29373292 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Nup37 | Mm_Celera | 10:88160429 | TCCAGTGCTGTCATT[A/G]ACATTGAACAAATGA | 69736 |
rs29373674 | snp | A/G | 0.48 | 0.0979796 | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145847 | ATTCCAGTCCTCATA[A/G]CTGTCCAGGCGCTTT | 69736 |
rs29375861 | snp | A/G | 0.188366 | 0.242283 | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145529 | TTTTCCCTAACTTCT[A/G]CATGCATACAGAACC | 69736 |
rs29383777 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Nup37 | Mm_Celera | 10:88156245 | GTAGAAAATCTTGTT[C/T]ACAAAGTGTTGAATT | 69736 |
rs45793081 | snp | A/G | 0.391111 | 0.206368 | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146113 | ATCCACTGTAGTTCC[A/G]GCTTTTCCAGGGTTA | 69736 |
rs45833256 | snp | A/G | 0.32 | 0.24 | intron-variant | Nup37 | Mm_Celera | 10:88178098 | ATTTTCTGAGTTAAG[A/G]CTTCACTGTGCTTCT | 69736 |
rs45916087 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nup37 | Mm_Celera | 10:88155061 | CTAACAGGCGTGAGC[A/G]TTCTGAGCCTCAACT | 69736 |
rs45935953 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nup37 | Mm_Celera | 10:88152100 | CAGTCTGTGAAGGCA[A/G]CTATGATTAGGCTCT | 69736 |
rs45956504 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Nup37 | Mm_Celera | 10:88149815 | CAGCGGTGTTTGGGG[G/T]GCATGACAAAGGAAG | 69736 |
rs45961904 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nup37 | Mm_Celera | 10:88174035 | TATGCATTTGGTTAC[A/G]TATTTCATATATTTC | 69736 |
rs46007634 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Nup37 | Mm_Celera | 10:88160024 | GTTATCATTTACTGT[A/G]GAACACACTCCTTGA | 69736 |
rs46011045 | snp | G/T | 0.32 | 0.24 | intron-variant | Nup37 | Mm_Celera | 10:88170549 | TTGAAAGTGGGAAAA[G/T]AACCATGAAAATATT | 69736 |
rs46025765 | snp | A/G | 0.391111 | 0.206368 | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145674 | TGTTCGCCTTTATGT[A/G]AGCACATGTGTATGG | 69736 |
rs46043121 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Nup37 | Mm_Celera | 10:88149803 | TCCATTCTGCTTCAG[A/C]GGTGTTTGGGGGGCA | 69736 |
rs46046212 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Nup37 | Mm_Celera | 10:88150181 | ACACATCTGTAAAAA[A/C]GTCATGAGTGTAGTA | 69736 |
rs46107273 | snp | A/C | 0.32 | 0.24 | intron-variant | Nup37 | Mm_Celera | 10:88177822 | ATAATTTAGGGGCTA[A/C]CAAGGAGTCCACTGC | 69736 |
rs46219875 | snp | C/T | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88148843 | GATTACATTTACAGC[C/T]GGCGTTCATCATAGC | 69736 |
rs46282698 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nup37 | Mm_Celera | 10:88170391 | AGCTAGCTCTCTTCT[C/T]TAAAGGATCATCAGG | 69736 |
rs46302904 | snp | A/C | 0.391111 | 0.206368 | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146445 | TTCTCCACGTCCATA[A/C]TTGGGACTACTTAAC | 69736 |
rs46306880 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Nup37 | Mm_Celera | 10:88177442 | AATTTTGCTTGCTTA[A/G]TTTGTGTAGATTGCA | 69736 |
rs46426638 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Nup37 | Mm_Celera | 10:88171634 | GACTCTCCTACTAAA[A/C]GCCTGTCACTTCACA | 69736 |
rs46442227 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145545 | CATGCATACAGAACC[C/T]TTTCAAAATAAGCCT | 69736 |
rs46499285 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Nup37 | Mm_Celera | 10:88177244 | TACTTTTCTATCCAT[A/G]GATCCCAAATTTGCA | 69736 |
rs46500103 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Nup37 | Mm_Celera | 10:88153245 | TAATGAGGCTTAACA[A/G]CTTTTTTGTTTGTCC | 69736 |
rs46538955 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146792 | AGATGCGTTCGCAGA[A/G]CAGCAGCCCGAATGC | 69736 |
rs46585967 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nup37 | Mm_Celera | 10:88154310 | CTTTGTTAAAATAAC[A/G]GCATTTGTTTGAAAC | 69736 |
rs46628657 | snp | A/G | 0.32 | 0.24 | intron-variant | Nup37 | Mm_Celera | 10:88171909 | TACATGTAATAATAC[A/G]TAGGTAATGACTTTA | 69736 |
rs46701200 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Nup37 | Mm_Celera | 10:88166831 | TCTTTCTGAAGATAG[G/T]CCAGTGCAGCATTTC | 69736 |
rs46751688 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nup37 | Mm_Celera | 10:88160509 | GTAAGTGTGCAGAGC[A/G]ACAGAAACATAATAA | 69736 |
rs46817809 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nup37 | Mm_Celera | 10:88149889 | TTCAAATGAAGTCAG[C/T]CGTTGATCCTGGAGA | 69736 |
rs46856554 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Nup37 | Mm_Celera | 10:88177548 | TAATGTGTATTTCAT[C/T]ATTACTATGCTTCTG | 69736 |
rs46865370 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146597 | AAGGATGCAACGACA[A/G]AAAATCTGAGAAGCC | 69736 |
rs46889740 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nup37 | Mm_Celera | 10:88165829 | TAATGGGTTAAGCTT[A/G]TGATTTTATAAATTC | 69736 |
rs46899162 | snp | A/G | 0.231111 | 0.249285 | utr-variant-5-prime, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88147038 | GGCCACCTATGGTCG[A/G]GAGAGCCTTGCCCAG | 69736 |
rs46965764 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88148709 | AAACAAGGTGATACT[A/G]AAAGGCTAAACAATT | 69736 |
rs46968491 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nup37 | Mm_Celera | 10:88149747 | AGAGAAGACAGATCA[C/T]ATTCTGGTGGAGTTC | 69736 |
rs47022011 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nup37 | Mm_Celera | 10:88149432 | GTTGAAAACGCAAGC[A/G]ACCAGAGGTAGGCTT | 69736 |
rs47032649 | snp | A/G | 0.32 | 0.24 | intron-variant | Nup37 | Mm_Celera | 10:88149838 | AAAGGAAGAGATCAA[A/G]TCTGTTCTTCCGTCA | 69736 |
rs47050756 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146655 | TCTAACGGACTAAAA[A/G]AAGATTTTGATGGGT | 69736 |
rs47056747 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88147769 | AAGGTCATATAATTC[A/G]AACAAATAATGTAGC | 69736 |
rs47087100 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Nup37 | Mm_Celera | 10:88167649 | CTACAGCTCTGCACT[C/G]TCCCTTCTGTTCTCC | 69736 |
rs47116137 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nup37 | Mm_Celera | 10:88171774 | TTAGAAATGACTTAA[A/G]TAGGCTTGCAACCTG | 69736 |
rs47216363 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nup37 | Mm_Celera | 10:88150503 | CCAACTCAAACGAGG[A/G]ACAGTTAGTAAAGAT | 69736 |
rs47226172 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nup37 | Mm_Celera | 10:88150253 | GAGTCGGAAAGCAGC[A/G]CCTTCTTAAAACTGC | 69736 |
rs47364259 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nup37 | Mm_Celera | 10:88158826 | GGATTTCAAAGGCTA[C/T]ACATACATAATCTGA | 69736 |
rs47369083 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nup37 | Mm_Celera | 10:88160076 | TAGAAAACTAAATGT[A/G]CTCCCTGTGTTACAA | 69736 |
rs47436544 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Nup37 | Mm_Celera | 10:88149908 | TGATCCTGGAGAGCT[G/T]AGTTTCCTCACTCTG | 69736 |
rs47454733 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nup37 | Mm_Celera | 10:88172556 | ACGTTCTCTCATAGA[A/G]TGCGAATGCCGTGTG | 69736 |
rs47503891 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88147549 | GATTGTGACAGGTGT[C/T]AATAACGTTAGTATC | 69736 |
rs47506630 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146319 | GCACTGGAGCAGAAA[A/G]TCTGAGACAGGTAGT | 69736 |
rs47705982 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nup37 | Mm_Celera | 10:88154995 | TTCTGTGAGCATAGC[C/T]GAGCTCTGCCTAATC | 69736 |
rs47735526 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nup37 | Mm_Celera | 10:88158793 | GCTGAGAGGCAAAGG[C/T]GGCACAGGAGAGGAC | 69736 |
rs47759359 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Nup37 | Mm_Celera | 10:88173875 | AGATAAAGCATATTC[A/T]TGGATAATAGCTATT | 69736 |
rs47766503 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146228 | CCTGTTGTGAAGACT[C/T]GATGAGACGCTGGAT | 69736 |
rs47874749 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Nup37 | Mm_Celera | 10:88156601 | CAAGCTGACAGCATA[C/T]ATTTATTGTTTTAAA | 69736 |
rs48086748 | snp | A/C | 0.244898 | 0.249948 | upstream-variant-2KB, utr-variant-5-prime | Nup37, Parpbp | Mm_Celera | 10:88146933 | AGAGGTTTGAATCGC[A/C]TCGGCGTCCCTTTCA | 69736 |
rs48105558 | snp | A/G | 0.244898 | 0.249948 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146668 | AAGAAGATTTTGATG[A/G]GTTTCGGTCTTGCCG | 69736 |
rs48115938 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nup37 | Mm_Celera | 10:88149077 | AATCCATATATGTGT[A/G]TTTTGTGGTTAGTAT | 69736 |
rs48123931 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Nup37 | Mm_Celera | 10:88156192 | CTTTATATTAAAAGG[A/C]AATATTCACAGTATA | 69736 |
rs48163998 | snp | C/G | 0.391111 | 0.206368 | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145104 | AAGGTATTCCTGCTG[C/G]CAACTGATACAACTC | 69736 |
rs48200333 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Nup37 | Mm_Celera | 10:88171246 | TCGGTCATGGAACTT[A/C]TGTTTCCTGACATGC | 69736 |
rs48205099 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nup37 | Mm_Celera | 10:88150478 | GCCAAACATTGTTTA[A/G]TAGACTGGACCAACT | 69736 |
rs48262606 | snp | A/G | 0.426035 | 0.177515 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146608 | GACAGAAAATCTGAG[A/G]AGCCTGCACTCGTCG | 69736 |
rs48267694 | snp | A/G | 0.32 | 0.24 | intron-variant | Nup37 | Mm_Celera | 10:88151433 | AACACTAATAGCCCT[A/G]TCTACTACTGAATCT | 69736 |
rs48299060 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nup37 | Mm_Celera | 10:88150687 | CAAGATAAGCTTAGA[C/T]GTCAGGATAACGTGA | 69736 |
rs48346646 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Nup37 | Mm_Celera | 10:88177180 | AGGTAATGGAAAATG[C/T]TTCCTGCCATTGCTG | 69736 |
rs48347177 | snp | C/T | 0.32 | 0.24 | intron-variant | Nup37 | Mm_Celera | 10:88167995 | AACCCTTGAAAATAT[C/T]TATGGTATCTCCTAT | 69736 |
rs48356984 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nup37 | Mm_Celera | 10:88150699 | AGACGTCAGGATAAC[A/G]TGAAAGGAGGGCCAG | 69736 |
rs48358403 | snp | A/T | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88148487 | TACAAGAAAAAAAAA[A/T]TTTTTGAAGATCTAC | 69736 |
rs48387616 | snp | A/T | | | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88148568 | GATAGATGTAAAAAC[A/T]ATGAAGGTCTTCTTT | 69736 |
rs48457218 | snp | C/T | 0.32 | 0.24 | intron-variant | Nup37 | Mm_Celera | 10:88170302 | TATTGAATCAGTGTA[C/T]AATTACAAACCATAA | 69736 |
rs48484566 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Nup37 | Mm_Celera | 10:88152120 | GATTAGGCTCTTACA[C/T]TTAATTTTAAACTGC | 69736 |
rs48496113 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146535 | ATCTCCATTAAAAGA[C/T]GACAGGTGACAGTTA | 69736 |
rs48523311 | snp | A/C | 0.231111 | 0.249285 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88147083 | TTTAGGTGCGTATCG[A/C]GTGCGGTGACCGGGG | 69736 |
rs48524228 | snp | A/C | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88148453 | ACCAAAGCTGAACTT[A/C]AAAGTATGTTGCTTT | 69736 |
rs48650065 | snp | C/G/T | 0.132653 | 0.220748 | intron-variant | Nup37 | Mm_Celera | 10:88158781 | CAAGGTTGGATGGCT[C/G/T]AGAGGCAAAGGCGGC | 69736 |
rs48672467 | snp | A/G | 0.336735 | 0.234472 | utr-variant-5-prime, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88148182 | TGACAGGCAATAAAC[A/G]ACTATTTGATTCTTA | 69736 |
rs48791097 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Nup37 | Mm_Celera | 10:88159617 | AGAGTGAAATGCAGG[A/T]AACTTGAAGAGAACA | 69736 |
rs48795814 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Nup37 | Mm_Celera | 10:88153671 | GAAACATTTCAGTGC[C/T]GGATTACTGTCCTTC | 69736 |
rs48825977 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145749 | TTGTTGACTTGCCCC[A/G]GCATCACTTGTCTAC | 69736 |
rs48911355 | snp | C/G | 0.408163 | 0.193609 | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146484 | AAGGCACCAGTGAAG[C/G]AAATAGCCAACCTCC | 69736 |
rs49042755 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nup37 | Mm_Celera | 10:88159354 | ACAGTTCTTCCTGGG[A/G]CCACTTTATATCTGT | 69736 |
rs49077287 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nup37 | Mm_Celera | 10:88175850 | TGTATGATTTGTGAG[A/G]ACTGTAAAGAAGGCC | 69736 |
rs49117802 | snp | A/G | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88147709 | GGGACTTTCCAGTTC[A/G]TCGGACCCTTGATAG | 69736 |
rs49164015 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Nup37 | Mm_Celera | 10:88151300 | TGTTCACCTAACAGA[C/G]CTTCCCCTGGCAAGG | 69736 |
rs49172989 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nup37 | Mm_Celera | 10:88158756 | CCAGAAGCGTCCTTA[C/T]GAGTTATGGCAAGGT | 69736 |
rs49184233 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nup37 | Mm_Celera | 10:88149498 | ATAGAATCTCATTGT[C/T]AAATACTGACAGATA | 69736 |
rs49237176 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nup37 | Mm_Celera | 10:88160622 | GAAAAGCAGTGATAT[A/G]AGGACAGATGCAATT | 69736 |
rs49267585 | snp | A/G | 0.336735 | 0.234472 | synonymous-codon | Nup37 | Mm_Celera | 10:88174466 | ATCTCTTCAGTCAGA[A/G]CAGACACCCTTAATG | 69736 |
rs49299039 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nup37 | Mm_Celera | 10:88151419 | TGCTTACCATTGAGA[A/G]CACTAATAGCCCTAT | 69736 |
rs49320476 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nup37 | Mm_Celera | 10:88155136 | CCACGATTCTGTGAT[C/T]GATGCCCAGTGTCCA | 69736 |
rs49349726 | snp | A/C | 0.231111 | 0.249285 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146753 | GCGCAGACAACGCCA[A/C]TGGCTGGCACGTCGC | 69736 |
rs49349857 | snp | A/C | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88147291 | TCCGGACCTCAAGTC[A/C]CCTGCATGCCTTATA | 69736 |
rs49390992 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nup37 | Mm_Celera | 10:88174989 | TAGGGTTCCACTGCC[A/G]GAATAAGTTCCTGGC | 69736 |
rs49469222 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Nup37 | Mm_Celera | 10:88173681 | CATTCTGTTTGAAAT[G/T]TGTTTTCCCTCTTGT | 69736 |
rs49522042 | snp | A/G | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88148878 | TCTGAGGTCTGTGTA[A/G]CCTGAGAACCTAGAC | 69736 |
rs49534046 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Nup37 | Mm_Celera | 10:88177467 | ATTGCAAAAATTTTT[G/T]ATTCTGGATCATACC | 69736 |
rs49560180 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88148148 | ACTTTGTAAATTTTG[C/T]TTGTGATCCACAGTT | 69736 |
rs49587282 | snp | C/T | 0.32 | 0.24 | intron-variant | Nup37 | Mm_Celera | 10:88168689 | CAGGGTTCTCAGTCT[C/T]TACCACGGTTTTTGG | 69736 |
rs49596598 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Nup37 | Mm_Celera | 10:88174727 | TCAGAGTGGTTCTAA[C/G]TCATGGCCATTGTTC | 69736 |
rs49628010 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Nup37 | Mm_Celera | 10:88149762 | CATTCTGGTGGAGTT[A/C]AGTACAACTGTGCCG | 69736 |
rs49654834 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nup37 | Mm_Celera | 10:88149398 | ATTAAAAACTTTCTC[C/T]AATGTGGACCACTTA | 69736 |
rs49684882 | snp | A/T | 0.32 | 0.24 | intron-variant | Nup37 | Mm_Celera | 10:88158649 | TCATGTGTTCCAGAA[A/T]AAAACGTTGGATTTG | 69736 |
rs49880979 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Nup37 | Mm_Celera | 10:88174666 | TGTCCTATGGAAATG[C/T]GTGTCTCCTGTAGAA | 69736 |
rs49889550 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Nup37 | Mm_Celera | 10:88161938 | ACCCGTTTGAATAGA[A/G]GCCTAAATAATAAAC | 69736 |
rs49965338 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Nup37 | Mm_Celera | 10:88152201 | ACAAATTATGAAGTA[A/C]TAAAACCTGGCAGTG | 69736 |
rs50011661 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nup37 | Mm_Celera | 10:88166561 | ACCGTGTAACTGGCT[A/G]GGAATACTAACTGAT | 69736 |
rs50068337 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nup37 | Mm_Celera | 10:88173471 | TTATGATCTAACTCC[A/G]CAATTTCAGTTAGTT | 69736 |
rs50069022 | snp | A/T | 0.32 | 0.24 | intron-variant | Nup37 | Mm_Celera | 10:88171222 | ATGCCGGAGGCACTT[A/T]GTTACCCATCGGTCA | 69736 |
rs50103738 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88147557 | CAGGTGTTAATAACG[C/T]TAGTATCACACATTA | 69736 |
rs50107641 | snp | C/T | 0.244898 | 0.249948 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146634 | CGTCGTGTGCCAGAT[C/T]CCCGATCTAACGGAC | 69736 |
rs50116555 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Nup37 | Mm_Celera | 10:88161186 | CTTCCTATGTACCTC[G/T]TGCCCTCTTTTTTTA | 69736 |
rs50132374 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Nup37 | Mm_Celera | 10:88151387 | TTGAATACACTTGAC[A/C]TGGAAACACTCTGGC | 69736 |
rs50153826 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nup37 | Mm_Celera | 10:88150688 | AAGATAAGCTTAGAC[A/G]TCAGGATAACGTGAA | 69736 |
rs50183865 | snp | A/G | 0.336735 | 0.234472 | downstream-variant-500B | Nup37 | Mm_Celera | 10:88178403 | GAAAAATATGTTCCT[A/G]TTGTGTTGGTGTACT | 69736 |
rs50309274 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146780 | TCGCTGTCACCGAGA[C/T]GCGTTCGCAGAGCAG | 69736 |
rs50328332 | snp | A/T | 0.244898 | 0.249948 | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146371 | GAGAGCACCACACTT[A/T]GCTAACTATCCCTGC | 69736 |
rs50405765 | snp | A/G | 0.32 | 0.24 | intron-variant | Nup37 | Mm_Celera | 10:88175332 | TAACATGCTAGTTAC[A/G]TGTTATTTGGTTATG | 69736 |
rs50458450 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Nup37 | Mm_Celera | 10:88149109 | AGCAGCAGTGGCAGT[C/T]ATACCCTCATATTTA | 69736 |
rs50468901 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nup37 | Mm_Celera | 10:88159603 | CAGGTCAGAGGAGAA[A/G]AGTGAAATGCAGGTA | 69736 |
rs50631496 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Nup37 | Mm_Celera | 10:88160678 | AGGCGCACTAGAAAA[A/G]AAAGACTGAGCTAGT | 69736 |
rs50690149 | snp | C/T | 0.244898 | 0.249948 | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145400 | CTTTGTTCCATCTCC[C/T]GTGTCCTGATGATGT | 69736 |
rs50772673 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nup37 | Mm_Celera | 10:88159251 | TGAGTGAGACACATG[A/G]CACTGACGTCAGCAA | 69736 |
rs50855644 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Nup37 | Mm_Celera | 10:88150364 | AATGAGAATGGTTTG[A/G]GCAGGCACGTTTTTG | 69736 |
rs50860104 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Nup37 | Mm_Celera | 10:88176340 | CTGTCAGGCGACCAC[C/T]AGCACTTGCTGGCTT | 69736 |
rs50866741 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nup37 | Mm_Celera | 10:88176334 | AGTCATCTGTCAGGC[A/G]ACCACCAGCACTTGC | 69736 |
rs50894806 | snp | C/G | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146191 | ATCAGGACTATGCCG[C/G]CCCCTCTGTTCTACC | 69736 |
rs50908849 | snp | C/T | 0.32 | 0.24 | intron-variant | Nup37 | Mm_Celera | 10:88169925 | AGATGGCCTTAAAGA[C/T]AGAAAATATGGGGCT | 69736 |
rs50927577 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Nup37 | Mm_Celera | 10:88154412 | ATGAAAGCATTTTTT[A/T]AAAAATTGGTTTTGA | 69736 |
rs50933498 | snp | A/T | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88148608 | TTCGTAGAGGTGTAT[A/T]CTGATAAAGTCCAAC | 69736 |
rs50936120 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Nup37 | Mm_Celera | 10:88177041 | TGTTGTCTGCAGGAC[A/G]GTGCTTACTGTAATG | 69736 |
rs50959573 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nup37 | Mm_Celera | 10:88161658 | TCTGGTTATTTGCTT[C/T]GTTTTTCCAGACAGG | 69736 |
rs51048741 | snp | A/G | 0.391111 | 0.206368 | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145452 | TGACACATGAAGAAA[A/G]TAATGTTCAATGACA | 69736 |
rs51117665 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nup37 | Mm_Celera | 10:88153514 | TAAAACATTTGCTGT[A/G]TCCATTTAGGAGGAA | 69736 |
rs51186872 | snp | A/T | 0.32 | 0.24 | intron-variant | Nup37 | Mm_Celera | 10:88169844 | TCTGTGCTTGTGTAC[A/T]AAGATTCATGTACTG | 69736 |
rs51222042 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nup37 | Mm_Celera | 10:88173827 | GCACCTGAATGAAAC[A/G]AACATTCTCAGAAAG | 69736 |
rs51295869 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nup37 | Mm_Celera | 10:88176939 | CAAGAAAGTATTCAT[A/G]GCTAAGTAAACTGGA | 69736 |
rs51312700 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Nup37 | Mm_Celera | 10:88171797 | GCAACCTGATTAATG[C/T]GTGTGCCACCACGCC | 69736 |
rs51330161 | snp | C/T | 0.391111 | 0.206368 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146555 | GGTGACAGTTATTCT[C/T]CTTGCCTGGTCCGGA | 69736 |
rs51349294 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nup37 | Mm_Celera | 10:88154915 | ACTCTTATAACACAC[A/G]GCTTTGCTCTGATGT | 69736 |
rs51362007 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nup37 | Mm_Celera | 10:88156211 | ATTCACAGTATATGT[A/G]CCTAGACAACAGCAA | 69736 |
rs51538464 | snp | A/T | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145570 | AAGCCTAGATGTGTC[A/T]GTATTCTAGGCAGCC | 69736 |
rs51548586 | snp | C/G | | | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88148871 | AGCTCTCTCTGAGGT[C/G]TGTGTAACCTGAGAA | 69736 |
rs51576313 | snp | C/G | | | intron-variant | Nup37 | Mm_Celera | 10:88164407 | AAATTACCATTTCTG[C/G]CACACTTAGGTTTAG | 69736 |
rs51632335 | snp | A/G | 0.244898 | 0.249948 | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145032 | CAAATGACCCCTCTG[A/G]GGAGACCTAACTCCC | 69736 |
rs51685087 | snp | C/T | 0.32 | 0.24 | intron-variant | Nup37 | Mm_Celera | 10:88154435 | GGTTTTGAGAGAAAT[C/T]ACACACTTAGAGAAC | 69736 |
rs51717112 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nup37 | Mm_Celera | 10:88174353 | AGCTGATGAGATACA[C/T]GTAGAATTTTCTTGT | 69736 |
rs51718744 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145438 | CAAATGTCTGGTTTT[A/G]ACACATGAAGAAAAT | 69736 |
rs51797261 | snp | C/G | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146151 | TTAGATCTGGCTGCC[C/G]AGGTATAAGAATGGT | 69736 |
rs51873629 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nup37 | Mm_Celera | 10:88149995 | ATTCATTCCCGTTCT[C/T]CCACCTCGAACCTTC | 69736 |
rs51892837 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Nup37 | Mm_Celera | 10:88151183 | AATTTCACAGCTATA[G/T]TAAAAATATTTAAAA | 69736 |
rs51940492 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Nup37 | Mm_Celera | 10:88151464 | GCTTCTCCCAAAACA[A/G]CTGCTTTTCTCATTG | 69736 |
rs51944096 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Nup37 | Mm_Celera | 10:88173952 | ATATTCTGTGACATG[C/T]TTTCATAAATCTAAG | 69736 |
rs51947710 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nup37 | Mm_Celera | 10:88155124 | TAACTTGCTTCTCCA[C/T]GATTCTGTGATTGAT | 69736 |
rs51983862 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Nup37 | Mm_Celera | 10:88178018 | TTTCATCAACACTTA[C/T]CAGCACTTATATTTA | 69736 |
rs51991331 | snp | C/T | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145484 | GAAGCTAGTAAATAG[C/T]CAAAAAAGCATAAAT | 69736 |
rs52043670 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nup37 | Mm_Celera | 10:88173749 | TAAATATTAGAACTT[A/G]GGTTTCTGACCAGTC | 69736 |
rs52056457 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Nup37 | Mm_Celera | 10:88174947 | AGGTAATGTCCTGTT[C/T]CTGCTGGAGTTGTGT | 69736 |
rs52369186 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nup37 | Mm_Celera | 10:88156565 | TTTTGGAACTTACAT[A/G]ATTTAAAGAATACTT | 69736 |
rs52579965 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nup37 | Mm_Celera | 10:88173035 | ACCCTTTCTTCTTCA[C/T]TTCTCATAGGTCCCC | 69736 |
rs52673743 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88162278 | CTATTCTGACTGGGG[G/T]TTCCCCTTCACCCAG | 69736 |
rs108231461 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88160616 | AAATGAGAAAAGCAG[G/T]GATATAAGGACAGAT | 69736 |
rs211741775 | snp | A/G | | | synonymous-codon, intron-variant | Nup37 | Mm_Celera | 10:88177079 | CTCTCTTAGGTGGTC[A/G]GCCATTAGTGAAAAC | 69736 |
rs211811628 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88155675 | GCTGTGCCTGGACCC[C/T]GTGTTCTGTCTCCAG | 69736 |
rs211851111 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88166232 | TTAGGAATGGGAGAA[A/G]GACAGGATGCAAATT | 69736 |
rs211873837 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88167408 | TCTATTAGAAAGCTC[C/T]GCCTCTGAACTTGGC | 69736 |
rs211922652 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88156689 | ATCAGGAATATAAAA[G/T]AAAAGCTTATTTTTA | 69736 |
rs211934854 | in-del | -/T | | | intron-variant | Nup37 | Mm_Celera | 10:88152789 | GGAAATCACAGATAC[-/T]TTACATTATGATTTC | 69736 |
rs211937259 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88178119 | CTGTGCTTCTTTGAT[C/T]CCCATGTTTTCCAGC | 69736 |
rs212003172 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88149165 | GAGACTTATTACATG[A/G]TTCCTCACGGAAAAC | 69736 |
rs212093288 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88157981 | GGGTGACAAACGTGG[A/T]CTAGCTTGGTGGCTT | 69736 |
rs212336724 | in-del | -/TTTTTTTTTTTTTTTT | | | intron-variant | Nup37 | GRCm38.p3 | 10:88162155 | GAAGGGCTTTTTCCC[-/TTTTTTTTTTTTTTTT]TTTTTTTTTTTTTGC | 69736 |
rs212368498 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88170862 | ACTGTCTCCTTTATA[A/T]AGAGAAAAGTGTCTT | 69736 |
rs212432619 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88159679 | AGAGTGGTGGTGGGC[G/T]GAGAATGAGCATGAT | 69736 |
rs212547572 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88149805 | CATTCTGCTTCAGCG[A/G]TGTTTGGGGGGCATG | 69736 |
rs212714983 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88150395 | TGGAGAAAAAAGAAA[C/T]AGAAAGATACCTTAA | 69736 |
rs212736055 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88169702 | CTTAGATCATACTCC[A/G]TCATTGAGAAAGTCA | 69736 |
rs212976661 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88162422 | AGTCAGAGAAAGAAA[A/C]AGAAAGGGAAAATAA | 69736 |
rs213133304 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88153031 | CAAAGGATCTTCCAC[A/G]TACTTAAAACACGTG | 69736 |
rs213269769 | in-del | -/TA | | | intron-variant | Nup37 | Mm_Celera | 10:88160593 | TTGTTATTTGAGCTT[-/TA]TATAGTAAATGAGAA | 69736 |
rs213293913 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88153982 | GCAGCAGACCCCATT[A/T]CAGATGGTTGTGAGC | 69736 |
rs213351202 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88171913 | TGTAATAATACATAG[A/G]TAATGACTTTAAATA | 69736 |
rs213528008 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88176179 | CTAAAACTGAACACT[G/T]GCAGAACACAGCTGA | 69736 |
rs213559289 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88175251 | CTGTACAAGTGCACT[C/T]AGACCCATGTGCACA | 69736 |
rs213697559 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88154835 | CAGCTCTTCATACGT[A/G]CAAAACAAGCACTGC | 69736 |
rs213706805 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146723 | GGGACACCGTGAAGT[C/T]GGGGCGAAGCCACTG | 69736 |
rs213739615 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88165087 | TCATTTGTTTTTCTT[A/G]CATTAGACTTAAGAA | 69736 |
rs213799192 | in-del | -/GTGTGTGT | | | intron-variant | Nup37 | GRCm38.p3 | 10:88154624 | AAACCAAGTTTTGAC[-/GTGTGTGT]GTGTGTGTGTGTGTG | 69736 |
rs213860968 | snp | A/T | | | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88147527 | GTCTCGAGACAAATT[A/T]GTTGAGGATTGTGAC | 69736 |
rs214081976 | in-del | -/TT | | | intron-variant | Nup37 | Mm_Celera | 10:88168788 | CTAGTTCTCAATGTC[-/TT]TTTTTTTTATAAGAA | 69736 |
rs214119095 | snp | C/G | | | downstream-variant-500B | Nup37 | Mm_Celera | 10:88178578 | ACACACTAGGTAGGA[C/G]AGAAAGAAGGTTAGA | 69736 |
rs214134284 | snp | C/G | | | intron-variant | Nup37 | Mm_Celera | 10:88166036 | AATTACAAAAGCTGT[C/G]AGAAGGAAACTCTCC | 69736 |
rs214260568 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88149345 | AATCATAAGTCATGC[A/G]TCAGGCAAATAATGT | 69736 |
rs214278520 | snp | C/G | | | intron-variant | Nup37 | Mm_Celera | 10:88155284 | ATTACAGAGTACAGG[C/G]AGCTGGGGAGATGAC | 69736 |
rs214381182 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88167605 | TGTCAACACCAGGGC[A/G]TTGTGAACGTGCCTT | 69736 |
rs214416789 | snp | C/G | | | intron-variant | Nup37 | Mm_Celera | 10:88149724 | GCTTTTTCCTTTTAT[C/G]AGCACATAGAGAAGA | 69736 |
rs214516656 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88157181 | ATGGGGGGTGAGGGG[C/T]GGGTAACTCAATAAT | 69736 |
rs214642276 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88171022 | CTTTAATTTTTAAAA[C/T]TTCTTTATAGTCCTA | 69736 |
rs214841743 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88158294 | ATAAAATTTCTTTGT[C/T]TCTGCAAAGTGAGCT | 69736 |
rs214842987 | in-del | -/A | | | intron-variant | Nup37 | Mm_Celera | 10:88162682 | TAAATATTTTTTAAT[-/A]ATTAATTTGTGTGTG | 69736 |
rs214880890 | snp | C/G | | | intron-variant | Nup37 | Mm_Celera | 10:88168296 | TTATAATTCATGCTG[C/G]GTGAGAGCTGCTGTT | 69736 |
rs215130126 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88173747 | ATTAAATATTAGAAC[A/T]TAGGTTTCTGACCAG | 69736 |
rs215139188 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88161146 | CAATAAAGTTTCCAT[C/T]CAATTACGGGATGCT | 69736 |
rs215241447 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88162602 | ATAATTTATATTTGT[A/T]TATATTTTATTACAT | 69736 |
rs215284555 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88151380 | TGGGGCATTGAATAC[A/C]CTTGACATGGAAACA | 69736 |
rs215375365 | in-del | -/CACACA | | | intron-variant | Nup37 | Mm_Celera | 10:88150861 | TAGCACACACGCGCG[-/CACACA]CACACACACACACAC | 69736 |
rs215395487 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88163704 | GTGAAAAGAACAACT[C/T]GAAGTCAAATGTGGA | 69736 |
rs215658231 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88165362 | AGGTATGGCATATGC[C/T]TATATTGGTCAATTG | 69736 |
rs215660510 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88177035 | GACCGTTGTTGTCTG[C/T]AGGACGGTGCTTACT | 69736 |
rs215697633 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88160546 | TAGAAAGACTCTGTC[G/T]CGGGAGCCCCAAAAT | 69736 |
rs215770073 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88166176 | AATATACCGTCCATA[C/T]ACTCTATAAAATATG | 69736 |
rs215815722 | in-del | -/G | | | intron-variant | Nup37 | Mm_Celera | 10:88150951 | AATATAAAGGTTATC[-/G]TAGACTTTGTCTTAT | 69736 |
rs215845266 | in-del | -/AG | | | intron-variant | Nup37 | Mm_Celera | 10:88170104 | TTGAGAGAGAGAGAG[-/AG]AATACGTTGAACTTC | 69736 |
rs215885739 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88154046 | CTCTAGAAGAGCAGT[C/T]CATGCTCTTAACCGC | 69736 |
rs215994729 | in-del | -/CTC | | | intron-variant | Nup37 | Mm_Celera | 10:88155084 | CCTCAACTCTTCTGT[-/CTC]CTCCTACTGCATTCT | 69736 |
rs216072796 | snp | A/G | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145765 | GCATCACTTGTCTAC[A/G]CCTCTAGCACACTGG | 69736 |
rs216243851 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88168402 | GACCTTAAAACCTTT[A/C]CCTCTAAAGCTAATT | 69736 |
rs216341910 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88158364 | TAAATTTACGTTTCA[A/G]AAGTTCTAATTGGTA | 69736 |
rs216343976 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88169631 | GTAAGGGTTTCTGTT[A/G]TAGTGATAGGACACC | 69736 |
rs216438784 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88153080 | TCTGTCGGTTGGTAA[A/G]GGATGTATAATTACT | 69736 |
rs216498938 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88159579 | GTCGCTTAAAGATAC[A/T]AGGAACAACAGGTCA | 69736 |
rs216603701 | in-del | -/G | | | intron-variant | Nup37 | Mm_Celera | 10:88176585 | TCTATAATGGGATCC[-/G]AATGCCCTCCTCCGG | 69736 |
rs216612607 | in-del | -/T | | | intron-variant | Nup37 | Mm_Celera | 10:88154737 | ATCCGTGGTGCAAGC[-/T]TGACTCTCCCACTTC | 69736 |
rs216696688 | in-del | -/T | | | intron-variant | Nup37 | Mm_Celera | 10:88162794 | AAAAACACCATTGAG[-/T]TTGTTTTGTGCTAGC | 69736 |
rs216710379 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88155452 | CCGGGCGTGGTGGCT[C/T]ACGCCTTTAATCCCA | 69736 |
rs216808072 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88160635 | ATAAGGACAGATGCA[A/G]TTAAAGAAAATGATG | 69736 |
rs216908777 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88161338 | TTATATCATATCTCA[G/T]ATCAGTTAATGCTCA | 69736 |
rs216973336 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88152737 | TGACCCATTTAGGGG[G/T]AGAATGGCCCTTTCA | 69736 |
rs217076229 | snp | A/G | | | downstream-variant-500B | Nup37 | Mm_Celera | 10:88178641 | TCCTGCTGATTAGGG[A/G]CATCAGGTTCCTTAG | 69736 |
rs217082744 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88156515 | TTGGTTTTTTTTCTT[G/T]TTTTTTTTTTTTTTT | 69736 |
rs217284474 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88163817 | TCTATATATATTCAG[C/T]TTGCTTGCTATTCTA | 69736 |
rs217354929 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88165059 | GTGAAGGATGAGCTG[A/C]CCTTTCTACAGTTCA | 69736 |
rs217360687 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88154134 | GACAAGATAGCACAG[A/T]GGGTAAAGGTCTTTG | 69736 |
rs217465628 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88154757 | TCTCCCACTTCTACC[A/G]CCCCAACATTGTGAG | 69736 |
rs217738518 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88149405 | ACTTTCTCCAATGTG[A/G]ACCACTTACGTGTTG | 69736 |
rs217865976 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88154326 | GCATTTGTTTGAAAC[A/T]GTAGCCAAGGACATA | 69736 |
rs217894035 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88164500 | AAGGTGGTTCATAGT[A/G]TAGCTGCCTTTGTTC | 69736 |
rs217961995 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88154922 | TAACACACGGCTTTG[C/T]TCTGATGTCCCCCAG | 69736 |
rs218198966 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88157414 | TTAGACCTACCATTG[C/T]AAACCATGGGCTTGT | 69736 |
rs218232815 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88171798 | CAACCTGATTAATGT[A/G]TGTGCCACCACGCCC | 69736 |
rs218267643 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88149424 | ACTTACGTGTTGAAA[A/C]CGCAAGCGACCAGAG | 69736 |
rs218300287 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88158731 | ACCCCTGAGCCTGCC[A/C]TCACCAGACCCAGAA | 69736 |
rs218300388 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88148759 | GCTTTCATAGATAAT[A/G]TTCAGCTTTCCTATT | 69736 |
rs218570266 | in-del | -/AA | | | intron-variant | Nup37 | Mm_Celera | 10:88173913 | GTCCAGCATACTTGG[-/AA]AAAAATCTTGTTCGT | 69736 |
rs218735928 | in-del | -/ACACACAC | | | downstream-variant-500B | Nup37 | GRCm38.p3 | 10:88178536 | TTCCCCCCCCCCACT[-/ACACACAC]ACACACACACACACA | 69736 |
rs218995037 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88151437 | CTAATAGCCCTATCT[A/G]CTACTGAATCTGCTT | 69736 |
rs219028856 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88150878 | ACACACACACACACA[C/T]GATAAAAGTAATGTA | 69736 |
rs219273685 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88153474 | AATGAAGTTCGGAGT[A/G]TTTTATTGTTTGTCT | 69736 |
rs219360922 | snp | G/T | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145293 | GTACAGTGACTATGG[G/T]TTTTGATGTTTTGTT | 69736 |
rs219377170 | snp | A/G | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145858 | CATAGCTGTCCAGGC[A/G]CTTTATCCAGTGAGC | 69736 |
rs219597916 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88176784 | AACCTCCATACATGG[C/T]AGATGCCTTGTATCT | 69736 |
rs219698408 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88165451 | AACGAACATACCAAG[A/T]CCTTTCTCAGCAAAG | 69736 |
rs219699356 | snp | C/G/T | | | intron-variant | Nup37 | GRCm38.p3 | 10:88177308 | GCTTAAACCAAAAGG[C/G/T]TTTTTTTCTTTTAAT | 69736 |
rs219745987 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88176526 | ACTGACTGTTCCAGA[A/G]GTCCTGAGTTCAATT | 69736 |
rs220035802 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88148618 | TGTATTCTGATAAAG[C/T]CCAACATAACTGAGC | 69736 |
rs220092367 | in-del | -/AAAAAAA | | | intron-variant | Nup37 | Mm_Celera | 10:88162444 | GGAAAATAAGAGTTG[-/AAAAAAA]AAAAAAAAAACAAAG | 69736 |
rs220108659 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88147852 | CCCAACACATGCTAA[A/G]TCTTTTAAATCCTCA | 69736 |
rs220338193 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88168099 | GAAGTTAATATTCTG[C/T]TGAAAAGCACTCAGC | 69736 |
rs220345289 | snp | C/T | | | downstream-variant-500B | Nup37 | Mm_Celera | 10:88178676 | AGTCCAGTCTTCTCT[C/T]ATCAAGCTATCCAAT | 69736 |
rs220374696 | snp | C/T | | | downstream-variant-500B | Nup37 | Mm_Celera | 10:88178726 | AACCACTTGACAAAC[C/T]ACAGCAGCAGGGGAA | 69736 |
rs220399358 | in-del | -/GGGGGGGGTGAT | | | intron-variant | Nup37 | Mm_Celera | 10:88157156 | AGCCTTATTTGCGGG[-/GGGGGGGGTGAT]GGGGGGTGAGGGGTG | 69736 |
rs220453656 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88168638 | CTTAGACATGGTAGA[C/T]AAGTACTCTGCCACA | 69736 |
rs220460011 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88177726 | TGGAGTTAGGGATGA[G/T]GTGAACAGCCGTGTG | 69736 |
rs220463788 | in-del | -/C | | | intron-variant | Nup37 | Mm_Celera | 10:88177172 | CACTCTCAGGTAATG[-/C]GAAAATGCTTCCTGC | 69736 |
rs220523267 | in-del | -/TAAAC | | | intron-variant | Nup37 | Mm_Celera | 10:88175501 | CTGAAATATCCCTAC[-/TAAAC]TAATCAGGACTCCAT | 69736 |
rs220633657 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88171452 | AGACAGTACAGAACC[A/C]GTACAGACAGGACAG | 69736 |
rs220678377 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88167013 | ATTAACTCAGTGAGC[A/G]AATTAATGCTAATGA | 69736 |
rs220733957 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88172381 | AAAGAAAAAAGAAAT[C/T]GAAGTTAAATCCATG | 69736 |
rs220781058 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88168527 | AACTGCCTGTTTCTT[C/T]CCACGCATTTGATCA | 69736 |
rs220818712 | in-del | -/A | | | intron-variant | Nup37 | Mm_Celera | 10:88155228 | GCTTTTATTTCTCTT[-/A]AAGAGTATAATTGCT | 69736 |
rs220878985 | in-del | -/T | | | intron-variant | Nup37 | Mm_Celera | 10:88161303 | CATACTGTGAAGTCA[-/T]TTCTCATATCACAGA | 69736 |
rs221071538 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88170066 | CAGCTACAGTGTACT[C/T]ACATCAAATAAATAA | 69736 |
rs221125935 | snp | G/T | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145148 | AGGCAGCTTATCCTG[G/T]GGAGACCCCATCAAC | 69736 |
rs221227254 | snp | C/G | | | intron-variant | Nup37 | Mm_Celera | 10:88160077 | AGAAAACTAAATGTA[C/G]TCCCTGTGTTACAAC | 69736 |
rs221476589 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88162992 | ACAGCTATAGCTATG[C/T]ACGCCTTGCGCATGC | 69736 |
rs221476665 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88175647 | CAATTCCCAGCACCC[G/T]CATGGCAGCTCATAC | 69736 |
rs221564061 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88176923 | CAACAGTAATGCAGA[A/G]CAAGAAAGTATTCAT | 69736 |
rs221583721 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88164158 | CCTAAAAAATTCTCT[A/G]GATAGCTCATCTCCT | 69736 |
rs221616331 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88166549 | TTTTCACGTGTGACC[A/G]TGTAACTGGCTAGGA | 69736 |
rs221647006 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88160711 | CAGTGTGTTAAGTGA[C/T]TGACTTCTCACCTCA | 69736 |
rs221647123 | in-del | -/GACCTTCCAG | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146693 | TGCCGAAGCCCTAGC[-/GACCTTCCAG]GTCTTTTTTTCCACG | 69736 |
rs221662048 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88157354 | CAGATGTTATATATG[C/T]TCAGAATGACTTAGA | 69736 |
rs221684890 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88167684 | CTTAGTTAATCAGCA[C/T]TCCAGTTCATGTGAT | 69736 |
rs221693422 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88172856 | TTTTTTTTTGTTGTT[C/T]TAGCTTTCTTTCATT | 69736 |
rs221956613 | snp | C/G | | | intron-variant | Nup37 | Mm_Celera | 10:88164074 | TTGAACTCAGGACCT[C/G]TGGAAGAACAACAGT | 69736 |
rs222022404 | in-del | -/T | | | intron-variant | Nup37 | Mm_Celera | 10:88175127 | TGAGCAGGACATGTA[-/T]TTTTTCAACCACTTA | 69736 |
rs222094472 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88154204 | ACTTGATGGAAGGAA[A/G]GCTAACTCTAGCAAG | 69736 |
rs222363412 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88174019 | ATTTATTGTATAAAT[G/T]TATGCATTTGGTTAC | 69736 |
rs222437133 | in-del | -/T | | | intron-variant | Nup37 | Mm_Celera | 10:88177485 | TCTGGATCATACCCA[-/T]TTTTTTATAGATAGC | 69736 |
rs222484039 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88162792 | TCCAAAAACACCATT[A/G]AGTTGTTTTGTGCTA | 69736 |
rs222587653 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88166406 | GACTTGTGAACCACC[A/G]CTTGATATGGGTGCT | 69736 |
rs222672542 | snp | C/G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88162739 | AACATGACCAGAAGG[C/G/T]GGGGGAGGGGGGGTG | 69736 |
rs222673805 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88151970 | TTCCATATCTAATCT[A/G]AGGAACGAACTCAGG | 69736 |
rs222716357 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88155990 | TCCCCCCAACACAGA[A/C]AGGGTTAATGTGGCC | 69736 |
rs222749076 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88158850 | AATCTGATTCTTTTT[C/T]CCTTTAGATTTTGTA | 69736 |
rs222749107 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88169912 | GTGTGACTTCATCAG[A/G]TGGCCTTAAAGATAG | 69736 |
rs222789852 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88168953 | AATTCATTTGCCAAG[A/G]TTTTGATAGTAGGGC | 69736 |
rs222868646 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88160014 | CCTTGCTGCAGTTAT[C/T]ATTTACTGTAGAACA | 69736 |
rs222895701 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88154991 | AGAGTTCTGTGAGCA[C/T]AGCTGAGCTCTGCCT | 69736 |
rs222930704 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88165564 | GCTATTTCTTCAGTC[A/T]CATACTTAACTGGTT | 69736 |
rs222942895 | in-del | -/T | | | intron-variant | Nup37 | Mm_Celera | 10:88162880 | CTTTGGATAAAGGTA[-/T]TCCTTTGTGAGCAGT | 69736 |
rs222994471 | in-del | -/T | | | intron-variant | Nup37 | Mm_Celera | 10:88161193 | GTACCTCGTGCCCTC[-/T]TTTTTTTAGATTGAA | 69736 |
rs223582459 | in-del | -/CACACA | | | intron-variant | Nup37 | Mm_Celera | 10:88150859 | TATAGCACACACGCG[-/CACACA]CGCACACACACACAC | 69736 |
rs223740324 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88159943 | TGGAAAACCAAAAAG[G/T]AAAAGGAAAAAGTGA | 69736 |
rs223764892 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88147304 | TCCCCTGCATGCCTT[A/G]TACCTCTCTGCTCTA | 69736 |
rs223795863 | in-del | -/AG | | | intron-variant | Nup37 | Mm_Celera | 10:88151297 | ATATGTTCACCTAAC[-/AG]AGCTTCCCCTGGCAA | 69736 |
rs223942452 | snp | A/G | | | intron-variant | Nup37 | GRCm38.p3 | 10:88153767 | ATTTAATAATTATGT[A/G]TTTATGTTTAGATTT | 69736 |
rs224115362 | in-del | -/GG | | | intron-variant | Nup37 | Mm_Celera | 10:88169364 | TACCTAATTTAGGGT[-/GG]GTTTTTTTTTTAAGT | 69736 |
rs224116317 | snp | C/G | | | intron-variant | Nup37 | GRCm38.p3 | 10:88150951 | AATATAAAGGTTATC[C/G]TAGACTTTGTCTTAT | 69736 |
rs224160715 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88161667 | TTGCTTCGTTTTTCC[A/C]GACAGGGTTTCTCAG | 69736 |
rs224168007 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88160724 | GACTGACTTCTCACC[A/T]CAATAGCCTTTCTAG | 69736 |
rs224263247 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88151496 | AATTATTCAGAGAGG[G/T]TTTTTTTGTTTTTTA | 69736 |
rs224367665 | in-del | -/AGAGAC | | | intron-variant | Nup37 | Mm_Celera | 10:88171705 | TGTGGGGAGAGAGGG[-/AGAGAC]AGAGACAGAGACAGA | 69736 |
rs224612002 | in-del | -/ATAA | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146256 | ATATGAACAAAACAG[-/ATAA]AAGGTGTCAGAGGGA | 69736 |
rs224724527 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88154243 | TCTCCACACAGCACC[A/G]TTGTGTGTACACATA | 69736 |
rs224853668 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88158079 | AGCAAATATCATGAA[A/C]GTTATACACAGGCTC | 69736 |
rs224972183 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88149176 | CATGGTTCCTCACGG[A/G]AAACCTAGGGTCCAC | 69736 |
rs225010500 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88154897 | TGTAGTTTTATAGTT[C/T]ATACTCTTATAACAC | 69736 |
rs225040479 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88151306 | CCTAACAGAGCTTCC[C/T]CTGGCAAGGTTTGAC | 69736 |
rs225043369 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88149947 | GATCCAAAACAAGTC[C/T]CTATTCTCTTGTCAG | 69736 |
rs225077375 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88149709 | AAGGAAAAACAAGAG[A/G]CTTTTTCCTTTTATG | 69736 |
rs225127327 | in-del | -/GCTT | | | intron-variant | Nup37 | Mm_Celera | 10:88151401 | CATGGAAACACTCTG[-/GCTT]GCTTACCATTGAGAA | 69736 |
rs225302409 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88148132 | CTGTTGAATGACAAA[C/T]ACTTTGTAAATTTTG | 69736 |
rs225512199 | snp | C/G | | | intron-variant | Nup37 | Mm_Celera | 10:88174660 | CCTCCATGTCCTATG[C/G]AAATGTGTGTCTCCT | 69736 |
rs225628097 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88175898 | TTTAGCAACTCTTCC[A/G]TATCATTAAAAACTC | 69736 |
rs225754609 | snp | A/T | | | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88148658 | TTTCTATGTATTAGA[A/T]ACACTTCAGATTTCC | 69736 |
rs226113600 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146547 | AGATGACAGGTGACA[G/T]TTATTCTTCTTGCCT | 69736 |
rs226225536 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88147037 | TGGCCACCTATGGTC[C/G]GGAGAGCCTTGCCCA | 69736 |
rs226258961 | snp | C/G | | | missense, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88148278 | GATTGCGAAGATTAT[C/G]TGCACGTGGTAGAAT | 69736 |
rs226261434 | in-del | -/TAAATAAA | | | intron-variant | Nup37 | GRCm38.p3 | 10:88169240 | AACCCTGTCTCAAAT[-/TAAATAAA]TAAATAAATAAATAA | 69736 |
rs226269493 | in-del | -/TT | | | intron-variant | Nup37 | GRCm38.p3 | 10:88168707 | CCACGGTTTTTGGGG[-/TT]TTTTTTTTTAATATT | 69736 |
rs226348704 | in-del | -/ACCAA | | | intron-variant | Nup37 | Mm_Celera | 10:88172362 | CAGTATGCAGTTTTC[-/ACCAA]AAAAAAGAAAAAAGA | 69736 |
rs226549769 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88177817 | TAATCATAATTTAGG[A/G]GCTAACAAGGAGTCC | 69736 |
rs226559075 | in-del | -/GA | | | intron-variant | Nup37 | Mm_Celera | 10:88149813 | TCAGCGGTGTTTGGG[-/GA]GGGCATGACAAAGGA | 69736 |
rs226604496 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88172792 | CTTTTTAAATTTAAG[A/G]CTGTTTCCTACCTAT | 69736 |
rs226645018 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88169441 | TGTTCATATTTTTTC[A/G]GTTTATATAATTATT | 69736 |
rs226682400 | in-del | -/A | | | intron-variant | Nup37 | Mm_Celera | 10:88168393 | CTTCTTTAAGACCTT[-/A]AAACCTTTCCCTCTA | 69736 |
rs226771196 | snp | C/T | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145241 | ACCAGCCCAAACTGC[C/T]GACCCACAGATTCAA | 69736 |
rs226902199 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88171513 | CTGCTAAGCATGGCC[A/C]TCTTGGGAGAAAACA | 69736 |
rs227114314 | in-del | -/GTGT | | | intron-variant | Nup37 | GRCm38.p3 | 10:88173065 | CTTTTGAGTTTCATG[-/GTGT]GTGTGTGTGTGTGTG | 69736 |
rs227185566 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88175770 | AAAATTTTTCTATAG[A/G]TTATTATGAAATAAT | 69736 |
rs227279500 | snp | C/G | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145534 | CCTAACTTCTGCATG[C/G]ATACAGAACCCTTTC | 69736 |
rs227590785 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88176149 | GGCTTCCTTATGCCA[C/T]TTATATCTCAGCCCC | 69736 |
rs227602320 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88176026 | GGGAGTGCAGACAGA[C/T]GGATCTAGGAGCTCA | 69736 |
rs227686777 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88174879 | CAAACTCTTGTTTTT[C/T]TAGTTATCCTCAAGA | 69736 |
rs227745206 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88173208 | TCTAAATGTTTATCA[A/G]TGGATAAAGGAAATG | 69736 |
rs227746705 | snp | A/C/T | | | intron-variant | Nup37 | GRCm38.p3 | 10:88161221 | GAATATTTATCAGCA[A/C/T]ATATACACCATTGGA | 69736 |
rs227755719 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88164997 | AATCGAGGTGGCGAT[G/T]CCTTAACCACATGCG | 69736 |
rs227795184 | in-del | -/CT | | | intron-variant | Nup37 | Mm_Celera | 10:88162949 | TTGTGTTCATTTCCC[-/CT]CTTAGTTCTGAGGCT | 69736 |
rs227799194 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88165073 | GACCTTTCTACAGTT[C/T]ATTTGTTTTTCTTAC | 69736 |
rs227842820 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88165819 | TCTACGTGGTTAATG[A/G]GTTAAGCTTATGATT | 69736 |
rs227846580 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88162127 | AGGCACACAGCATCG[A/C]TGGCTGCTCTCAGAA | 69736 |
rs228169278 | in-del | -/TGT | | | intron-variant | Nup37 | Mm_Celera | 10:88151156 | ATTACAAGGAAATGT[-/TGT]ATTCGGAAACAAATT | 69736 |
rs228218637 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88165933 | CTGTAAGAACAATTC[A/G]GATCAACAGATATTT | 69736 |
rs228234940 | snp | A/G | | | missense, synonymous-codon | Nup37 | Mm_Celera | 10:88178152 | GTCCTCATTGGTTCT[A/G]TAGCTGTCGGTTCTG | 69736 |
rs228362479 | snp | C/G | | | intron-variant | Nup37 | Mm_Celera | 10:88176969 | AGGTCTGCATGGAAA[C/G]TCACAGAGGATCGTG | 69736 |
rs228454462 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88167309 | GTCAAAGTTTTCTAC[A/G]ATCTAAGCTATAGAA | 69736 |
rs228534835 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88169115 | AGCCAGGCAGTGGTG[A/G]TGTATGCCTTTAATC | 69736 |
rs228545376 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88168147 | AGACCCTATAAAATT[A/G]AAGTAAGTATAATTC | 69736 |
rs228605886 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88157950 | GTTACTTAGATGTTT[C/T]CATTTTCTTTATGAG | 69736 |
rs228748768 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88159138 | GAGCTGGGTCATATA[C/T]AGGAGTCTGCATGCT | 69736 |
rs228814876 | in-del | -/ATATAAGC | | | intron-variant | Nup37 | Mm_Celera | 10:88162631 | TATTTAATATATATT[-/ATATAAGC]ATATAATTATATATT | 69736 |
rs228871215 | in-del | -/C | | | intron-variant | Nup37 | Mm_Celera | 10:88161864 | ACCTGCTAAATTTTT[-/C]TTGTGAGGGACATGA | 69736 |
rs228975944 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88169666 | CAAAAGGAACTGGGG[A/G]GGGGGGGGAGGCTTA | 69736 |
rs229051323 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88160252 | AGCATATATATGCAC[A/T]CACACATGTTTTCTG | 69736 |
rs229115402 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88168252 | TGTTTTAATTTATGG[A/G]TTAAAGGTGTTGAAG | 69736 |
rs229121034 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88151087 | TTTCGGACAACAGTT[C/T]TCTATAAGTTGATAA | 69736 |
rs229155905 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88160845 | CATTGTAGACAATCC[A/G]TTCTTGCTTACCAGC | 69736 |
rs229308677 | in-del | -/TA | | | downstream-variant-500B | Nup37 | Mm_Celera | 10:88178427 | GTGTACTTTTTGAGC[-/TA]TGTTTGGTTTTGTTT | 69736 |
rs229430634 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88161009 | CATTTTTCTTTTCTC[A/G]TTTTTTGATAAACAT | 69736 |
rs229434520 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88162312 | CTCAGAGCTCCTTCC[C/T]CACCCACCTAAACTA | 69736 |
rs229490624 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88171628 | GGAAATGACTCTCCT[A/G]CTAAAAGCCTGTCAC | 69736 |
rs229579981 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88152897 | CTATATTAAAGTGTC[A/G]CAGCATTAGGGAGGT | 69736 |
rs229580079 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88163450 | TTCCTCTGTTGCACA[A/T]TGTATCTTGAAGACA | 69736 |
rs229702245 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88170972 | TGATATATCAAATTT[A/G]ACAATCTTTACTTTT | 69736 |
rs229809346 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88162771 | TGTGTGGGCCGGGAG[A/C]CGACTTCCAAAAACA | 69736 |
rs229845161 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88160453 | CAAATGATACAAACA[G/T]TAGAGGTGAACTTCA | 69736 |
rs229942296 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88162076 | GTGTGTCCCTGCAAA[A/G]CCCAGGAGGAAGCTG | 69736 |
rs230019670 | snp | C/G | | | intron-variant | Nup37 | Mm_Celera | 10:88154787 | GTTCAGCACTATACC[C/G]AACACGTTCACGTGG | 69736 |
rs230021609 | snp | A/T | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146106 | TGCCAATATCCACTG[A/T]AGTTCCAGCTTTTCC | 69736 |
rs230023289 | in-del | -/AAAC | | | intron-variant | Nup37 | Mm_Celera | 10:88155584 | GAAAAACCAAAAAAT[-/AAAC]AAACAAACAAACAAA | 69736 |
rs230034593 | in-del | -/TTTG | | | intron-variant | Nup37 | Mm_Celera | 10:88168563 | ACTAACAGCTCTGTT[-/TTTG]TTTGTTTGTTTGCTT | 69736 |
rs230048518 | in-del | -/AGA | | | intron-variant | Nup37 | Mm_Celera | 10:88177685 | GGTGCTTTCGGGGTC[-/AGA]AGAAGTTATGGATCC | 69736 |
rs230104647 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88154143 | GCACAGTGGGTAAAG[A/G]TCTTTGCCACCAAGC | 69736 |
rs230115975 | in-del | -/GA | | | intron-variant | Nup37 | Mm_Celera | 10:88170091 | AAATAAATAAATCTT[-/GA]GAGAGAGAGAGAGAA | 69736 |
rs230191176 | in-del | -/TCTTA | | | downstream-variant-500B | Nup37 | Mm_Celera | 10:88178673 | GAAAGTCCAGTCTTC[-/TCTTA]TCAAGCTATCCAATT | 69736 |
rs230327198 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88154014 | ACCATGTGGTTGCTG[A/G]GAATCGAACTCAGGA | 69736 |
rs230382890 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88163561 | GTTCCAGGAAGGGGG[A/T]CAACCAGCTTGACTT | 69736 |
rs230409917 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88155737 | CTGCAGCTTTTCTGC[C/T]ATTCTGTACTCCCAA | 69736 |
rs230431658 | in-del | -/G | | | intron-variant | Nup37 | Mm_Celera | 10:88169365 | TACCTAATTTAGGGT[-/G]TTTTTTTTTTAAGTT | 69736 |
rs230507876 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88147788 | AAATAATGTAGCATA[A/G]TCCTGAGATAGGCAG | 69736 |
rs230509738 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88156694 | GAATATAAAAGAAAA[A/G]CTTATTTTTATATCA | 69736 |
rs230532208 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88164803 | AATGTGAAAAATATG[C/T]ACATTATGCAAACAA | 69736 |
rs230548662 | in-del | -/CAGA | | | intron-variant | Nup37 | Mm_Celera | 10:88155142 | TCTGTGATTGATGCC[-/CAGA]CAGTGTCCAGATTTT | 69736 |
rs230676223 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88154413 | TGAAAGCATTTTTTA[A/T]AAAATTGGTTTTGAG | 69736 |
rs230715227 | in-del | -/TT | | | intron-variant | Nup37 | Mm_Celera | 10:88177218 | GGTTTTCAAATTGGA[-/TT]TTTTTTTTTTACTTT | 69736 |
rs230885344 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88166082 | TTAAAAATATTGGAT[A/G]AAGTTTTACAATGAG | 69736 |
rs231079014 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88157799 | AGAATATGTGACGAG[C/T]ATCTTGACAAAAGAC | 69736 |
rs231124217 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88150405 | AGAAACAGAAAGATA[C/T]CTTAATCCTTTGATA | 69736 |
rs231157356 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88149834 | TGACAAAGGAAGAGA[A/T]CAAATCTGTTCTTCC | 69736 |
rs231254989 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88156326 | TGTGGGGCTTCCCTG[A/G]CCTAGTCACTGCATC | 69736 |
rs231299325 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88167203 | TGCTAACTTCAGAGT[A/G]TATTTGAAAATCTGA | 69736 |
rs231633374 | in-del | -/AGAC | | | intron-variant | Nup37 | Mm_Celera | 10:88171713 | GAGAGGGAGAGACAG[-/AGAC]AGAGACAGAGACAGA | 69736 |
rs231966311 | snp | C/G | | | intron-variant | Nup37 | Mm_Celera | 10:88149738 | TGAGCACATAGAGAA[C/G]ACAGATCACATTCTG | 69736 |
rs232007279 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88159258 | GACACATGGCACTGA[C/T]GTCAGCAAAGAACAG | 69736 |
rs232051117 | in-del | -/T | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146217 | CTACCTCCCAGCCTG[-/T]TGTGAAGACTCGATG | 69736 |
rs232077753 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88152647 | TTCATGGTCTCTACA[C/T]TAGAGACCATGAAAA | 69736 |
rs232195352 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88147534 | GACAAATTAGTTGAG[A/G]ATTGTGACAGGTGTT | 69736 |
rs232378522 | in-del | -/TA | | | intron-variant | Nup37 | Mm_Celera | 10:88164623 | GTGTGTGTGTGTGTG[-/TA]TGTGTGTATACATGT | 69736 |
rs232392479 | in-del | -/TGT | | | intron-variant | Nup37 | GRCm38.p3 | 10:88151153 | CTAATTACAAGGAAA[-/TGT]TGTATTCGGAAACAA | 69736 |
rs232407425 | in-del | -/CTGG | | | intron-variant | Nup37 | Mm_Celera | 10:88151058 | CAAATGCTTTAGGCT[-/CTGG]CTAGGAGCTATCTTT | 69736 |
rs232445471 | snp | A/G | | | downstream-variant-500B | Nup37 | Mm_Celera | 10:88178583 | CTAGGTAGGACAGAA[A/G]GAAGGTTAGAGCGAC | 69736 |
rs232517346 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88168303 | TCATGCTGGGTGAGA[A/G]CTGCTGTTGCCTTTT | 69736 |
rs232665172 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88154445 | GAAATTACACACTTA[A/G]AGAACCTAAGTTCAA | 69736 |
rs232690296 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88176286 | AGAGAATTTTTTTTT[C/T]CCTCAGGCCTTCTTT | 69736 |
rs232754349 | in-del | -/ATGC | | | intron-variant | Nup37 | Mm_Celera | 10:88176142 | TGCTATGGCTTCCTT[-/ATGC]ATGCCACTTATATCT | 69736 |
rs232816106 | snp | C/T | | | synonymous-codon | Nup37 | Mm_Celera | 10:88153541 | GGAAGAAACAGACAT[C/T]GAAGGGATTCAGTAT | 69736 |
rs232966805 | snp | G/T | | | downstream-variant-500B | Nup37 | Mm_Celera | 10:88178814 | CCCAGAATTCCAAAT[G/T]TAAACTATCTGCAGC | 69736 |
rs233143351 | in-del | -/T | | | intron-variant | Nup37 | Mm_Celera | 10:88155953 | TGTGAAGATGTTCTG[-/T]TTTTTTCTAGATTTT | 69736 |
rs233214338 | in-del | -/TGTGTGTGT | | | intron-variant | Nup37 | GRCm38.p3 | 10:88154623 | AAACCAAGTTTTGAC[-/TGTGTGTGT]GTGTGTGTGTGTGTG | 69736 |
rs233428529 | snp | C/G | | | intron-variant | Nup37 | Mm_Celera | 10:88155046 | CGGAATGTGCTCTTT[C/G]TAACAGGCGTGAGCG | 69736 |
rs233521163 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88170713 | CCAATAGTGATAAGA[A/C]TTACGCTAGCCCAAT | 69736 |
rs233538341 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88173764 | AGGTTTCTGACCAGT[C/T]CCCACTCTTTCCACT | 69736 |
rs233564354 | snp | C/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88147148 | CCCTGTTCTCCAGAG[C/T]TCTTCCTTGTGACCT | 69736 |
rs233582078 | in-del | -/ATG | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145984 | TGAGCTATGGGTGAT[-/ATG]ATTAGTTTGCCTGAA | 69736 |
rs233604445 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88163723 | GTCAAATGTGGATAC[A/G]AGCTGACGTCTTTGT | 69736 |
rs233684879 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88162608 | TATATTTGTATATAT[G/T]TTATTACATATTTAA | 69736 |
rs234134963 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88169866 | CATGTACTGTCTGTA[C/T]GTATGATCTACTTCA | 69736 |
rs234146442 | in-del | -/GGGGGGTGA | | | intron-variant | Nup37 | Mm_Celera | 10:88157158 | CCTTATTTGCGGGGG[-/GGGGGGTGA]TGGGGGGTGAGGGGT | 69736 |
rs234153399 | in-del | -/TT | | | intron-variant | Nup37 | GRCm38.p3 | 10:88168837 | AACTAGACCAGTAGG[-/TT]TTTTTTTGTTTTGTT | 69736 |
rs234177594 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88173331 | ACAAAGTAAATAAGT[A/C]AGACTTATTCTTGTG | 69736 |
rs234308739 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88171030 | TTTAAAACTTCTTTA[A/T]AGTCCTAAAGAAGTC | 69736 |
rs234612932 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88167883 | AATGAGCTGCCAACT[C/T]AAATAGACAGTAAAC | 69736 |
rs234730855 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88168434 | CAAGCATTTACATAT[A/G]TACACATGTCCATTT | 69736 |
rs234897019 | snp | C/G | | | intron-variant | Nup37 | Mm_Celera | 10:88158626 | CAAGCCCAGAATGTC[C/G]GGACACTTCATGTGT | 69736 |
rs235021973 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88176578 | CACAACCATCTATAA[G/T]GGGATCCAATGCCCT | 69736 |
rs235286208 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88167515 | TAAAGAATAGTCCAC[C/T]GCTTTCTGTAATCAG | 69736 |
rs235336872 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88165364 | GTATGGCATATGCCT[A/G]TATTGGTCAATTGGG | 69736 |
rs235355517 | in-del | -/TAAT | | | intron-variant | Nup37 | Mm_Celera | 10:88172482 | AGCTTTCTAAAGTAC[-/TAAT]TAATGAGTTTTAAAT | 69736 |
rs235398062 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88155505 | CGGATTTCTGAGTTC[A/G]AGGCTAGCCTGGTCT | 69736 |
rs235469562 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88166177 | ATATACCGTCCATAC[A/G]CTCTATAAAATATGA | 69736 |
rs235469614 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88154903 | TTTATAGTTCATACT[C/T]TTATAACACACGGCT | 69736 |
rs235630157 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88169736 | TAAGAATTCGGGTTG[A/G]AAACAAAAATAGGAG | 69736 |
rs235668798 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88160847 | TTGTAGACAATCCAT[G/T]CTTGCTTACCAGCCC | 69736 |
rs235733588 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88151971 | TCCATATCTAATCTG[A/G]GGAACGAACTCAGGC | 69736 |
rs235758093 | in-del | -/GTGTGTGTGTGT | | | intron-variant | Nup37 | GRCm38.p3 | 10:88173619 | CATGTGCATGTGTGA[-/GTGTGTGTGTGT]GTGTGTGTGTGTGTG | 69736 |
rs235783743 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88161954 | GCCTAAATAATAAAC[G/T]GACTATTTAAAGCAA | 69736 |
rs235795376 | in-del | -/CAG | | | intron-variant | Nup37 | Mm_Celera | 10:88149220 | GCACTGAAGGCTCAA[-/CAG]CACCACCCCATCTTC | 69736 |
rs235812462 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88159863 | TGGGTCTCTGAGTTC[A/G]AGGCCAGCCTGCTCT | 69736 |
rs235845172 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88153264 | TTTTGTTTGTCCATT[C/T]ATATTTCTTTTGCCT | 69736 |
rs235852314 | in-del | -/TTTTT | | | intron-variant | Nup37 | Mm_Celera | 10:88172836 | TTGGATATATTTTCC[-/TTTTT]TTTTTTTTTGTTGTT | 69736 |
rs236042371 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88175014 | CCTGGCCTCCTCTTC[A/G]GTGCAGTTTGGGGAT | 69736 |
rs236175337 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88163958 | GTAAAGATTTATTTA[C/T]TTTATGTATATGAGT | 69736 |
rs236192244 | in-del | -/GAAGTGTTCCTTAAATCCAGTTA | | | intron-variant | Nup37 | Mm_Celera | 10:88163386 | CGGGTCTCGTCTTTT[-/GAAGTGTTCCTTAAATCCAGTTA]GTGATTGGCTGCTCA | 69736 |
rs236316734 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88171958 | TCATTTATTTTATTT[G/T]GTAGTGATGTATTTA | 69736 |
rs236386989 | in-del | -/GC | | | intron-variant | Nup37 | Mm_Celera | 10:88163671 | GGAGACGGGGAGTAA[-/GC]GAAGGGGTCTAAGGG | 69736 |
rs236515857 | in-del | -/G | | | intron-variant | Nup37 | Mm_Celera | 10:88152216 | CTAAAACCTGGCAGT[-/G]GTTTTTTTTTTTTTT | 69736 |
rs236551571 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88160659 | AATGATGTGTTTTAT[C/T]TAAAGGCGCACTAGA | 69736 |
rs236627764 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88151424 | ACCATTGAGAACACT[A/G]ATAGCCCTATCTACT | 69736 |
rs236630983 | in-del | -/GGTGA | | | intron-variant | Nup37 | GRCm38.p3 | 10:88166310 | CTTTGGTATATGTGG[-/GGTGA]GGTGAGGTAGTTGTG | 69736 |
rs236713940 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88150701 | ACGTCAGGATAACGT[A/G]AAAGGAGGGCCAGGG | 69736 |
rs236715582 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88161500 | CTGAATGCACCTTGA[A/G]TTCTTTCTGTTTTTA | 69736 |
rs236784430 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88166248 | GACAGGATGCAAATT[C/T]TTTCTTAAAGAGATA | 69736 |
rs236821739 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88154206 | TTGATGGAAGGAAGG[C/T]TAACTCTAGCAAGTC | 69736 |
rs236846042 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88156277 | GGCTGTGCAGGGCTT[A/C]CCTGACCCACTCACT | 69736 |
rs236913900 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88164083 | GGACCTCTGGAAGAA[C/T]AACAGTCAGTGCTCT | 69736 |
rs237095062 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88149425 | CTTACGTGTTGAAAA[C/T]GCAAGCGACCAGAGG | 69736 |
rs237098809 | snp | C/G | | | intron-variant | Nup37 | Mm_Celera | 10:88155341 | TGCATTTGGTTCCTT[C/G]CACACACGTAGTGGG | 69736 |
rs237500113 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88168613 | AGGTGCTGGGGCTCT[A/G]ACCCAAGCCCTTAGA | 69736 |
rs237512332 | in-del | -/G | | | intron-variant | Nup37 | Mm_Celera | 10:88169735 | TTAAGAATTCGGGTT[-/G]GAAACAAAAATAGGA | 69736 |
rs237515476 | in-del | -/TTTTT | | | intron-variant | Nup37 | Mm_Celera | 10:88153891 | CTCTACTTCTTATTC[-/TTTTT]TTTTTTTTTTTTTAA | 69736 |
rs237665718 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88158295 | TAAAATTTCTTTGTT[A/T]CTGCAAAGTGAGCTC | 69736 |
rs237693043 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88154933 | TTTGCTCTGATGTCC[C/T]CCAGTTCATCTCTAA | 69736 |
rs237781959 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88154356 | ATTCTCATGTTTAGC[A/C]TAGCATTCATGTCTA | 69736 |
rs237853943 | snp | A/G | | | upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88146968 | TCGCGGCACGACCTG[A/G]GAACCAATCGCCGCG | 69736 |
rs238003152 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88171280 | CTCCACTCAGCACAG[C/T]GTAACAGTGGCTGAC | 69736 |
rs238104420 | snp | A/C/G | | | downstream-variant-500B | Nup37 | GRCm38.p3 | 10:88178677 | GTCCAGTCTTCTCTT[A/C/G]TCAAGCTATCCAATT | 69736 |
rs238117206 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88160567 | GCCCCAAAATGTTTC[G/T]GCAACTTCACTTGTT | 69736 |
rs238141186 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88177749 | GCCGTGTGGAGGCTA[A/G]GTTTTAAACCCTGGG | 69736 |
rs238215582 | snp | A/T | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145333 | ACTGATAATAAGCCA[A/T]CGAACAAATGAAGCT | 69736 |
rs238273768 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88150650 | TCAGTACTAGAATTC[A/T]GTTAGAATATAACAG | 69736 |
rs238325810 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88162513 | ACACAGGATGAATCC[C/T]ATGAAAACCCAAAAC | 69736 |
rs238363637 | snp | G/T | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146190 | AATCAGGACTATGCC[G/T]CCCCCTCTGTTCTAC | 69736 |
rs238482954 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88153044 | ACATACTTAAAACAC[G/T]TGTATGTGCTCAGTT | 69736 |
rs238554426 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88175912 | CGTATCATTAAAAAC[C/T]CAGACTCAGTGCTGG | 69736 |
rs238669848 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88176820 | TGTAGAGACCATGTT[A/C]CATGCAGATGCCTGT | 69736 |
rs238715870 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88153081 | CTGTCGGTTGGTAAG[G/T]GATGTATAATTACTC | 69736 |
rs238746107 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88166407 | ACTTGTGAACCACCA[C/T]TTGATATGGGTGCTG | 69736 |
rs238860631 | snp | A/T | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145225 | AGGAATCAATAACTT[A/T]ACCAGCCCAAACTGC | 69736 |
rs238885811 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88165190 | AATTATGAGAATTGA[C/T]AAATTTGTATCTAGT | 69736 |
rs238890300 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88150891 | CACGATAAAAGTAAT[G/T]TAAAAGGCAGAATGA | 69736 |
rs238987031 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88154880 | GCAACCCCAGCTCTG[A/C]GTGTAGTTTTATAGT | 69736 |
rs239012231 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88149950 | CCAAAACAAGTCCCT[A/G]TTCTCTTGTCAGTTT | 69736 |
rs239260744 | in-del | -/GTGTGTGTGTGTGTGT | | | intron-variant | Nup37 | GRCm38.p3 | 10:88173618 | CATGTGCATGTGTGA[-/GTGTGTGTGTGTGTGT]GTGTGTGTGTGTGTG | 69736 |
rs239347570 | in-del | -/AGAG | | | intron-variant | Nup37 | Mm_Celera | 10:88150211 | AGGGCCAGGAAACTA[-/AGAG]AGAGAGATTCTTGCC | 69736 |
rs239508748 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88157221 | ACCCAGGAACTTTGT[A/T]GATAACAACATTGTG | 69736 |
rs239873050 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88160797 | GTTAAAATATTATAG[A/G]AAACAGTATGGAGTG | 69736 |
rs239910870 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88171475 | CAGGACAGTGCTTCT[C/T]TAGTCCATCTTTAAT | 69736 |
rs239989550 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88161714 | CTGGAACTCACTCTT[C/T]AGACCAGGATGTCCT | 69736 |
rs240102034 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88149777 | CAGTACAACTGTGCC[A/G]TTCCTCGTGTTCCAT | 69736 |
rs240279091 | in-del | -/GT | | | intron-variant | Nup37 | GRCm38.p3 | 10:88168836 | GAACTAGACCAGTAG[-/GT]TTTTTTTTGTTTTGT | 69736 |
rs240357783 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88171212 | GGGGACCGAAATGCC[A/G]GAGGCACTTTGTTAC | 69736 |
rs240375171 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88159998 | AAGGGTAGGTCAGTG[A/G]CCTTGCTGCAGTTAT | 69736 |
rs240499176 | snp | C/T | | | downstream-variant-500B | Nup37 | Mm_Celera | 10:88178754 | GAAAGCAACCGCTGC[C/T]GCAGGCCCTCTCAGG | 69736 |
rs240571894 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88168643 | ACATGGTAGATAAGT[A/G]CTCTGCCACAGAGGG | 69736 |
rs240605154 | in-del | -/TTTTTTTT | | | intron-variant | Nup37 | GRCm38.p3 | 10:88152217 | AAAACCTGGCAGTGG[-/TTTTTTTT]TTTTTTTTTTTTTTT | 69736 |
rs240605200 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88168107 | TATTCTGCTGAAAAG[A/C]ACTCAGCCTGAAATG | 69736 |
rs240615514 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88151381 | GGGGCATTGAATACA[A/C]TTGACATGGAAACAC | 69736 |
rs240772798 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88171532 | TGGGAGAAAACATTA[A/G]AGAAGTCAGACAGAT | 69736 |
rs240995300 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88165851 | TATAAATTCATCAAT[A/G]AAGAAAATCCTATTC | 69736 |
rs241092678 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88166658 | TGTGTATCACATGCT[A/T]GCAAGTTCTTGCCAG | 69736 |
rs241151512 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88157362 | ATATATGCTCAGAAT[A/G]ACTTAGAGAGTGAAG | 69736 |
rs241337773 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88154048 | CTAGAAGAGCAGTCC[A/G]TGCTCTTAACCGCCG | 69736 |
rs241484417 | snp | A/G | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145771 | CTTGTCTACACCTCT[A/G]GCACACTGGGGTTGC | 69736 |
rs241546190 | snp | G/T | | | synonymous-codon | Nup37 | Mm_Celera | 10:88174526 | CAAAGTTGGTGCTGT[G/T]GCAGGAAATGATTGG | 69736 |
rs241601148 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88174367 | ATGTAGAATTTTCTT[G/T]TTCCACCCTGTATTA | 69736 |
rs241659498 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88176490 | CTGGAGGTCTGGTGA[A/G]ATGGCTCAGCGGTTA | 69736 |
rs241673266 | in-del | -/T | | | intron-variant | Nup37 | Mm_Celera | 10:88178072 | AAAAAGAAAAAAAAA[-/T]AGTTTTCTTTATTTT | 69736 |
rs241673519 | snp | C/G | | | intron-variant | Nup37 | Mm_Celera | 10:88164367 | CAGATCTCTTTGTAT[C/G]CTAGTTGGGTAGAAC | 69736 |
rs241708858 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88163232 | TGATGACTAACCAAA[A/G]CATTCATCTATGAGT | 69736 |
rs241797823 | in-del | -/C | | | intron-variant | Nup37 | Mm_Celera | 10:88156140 | TTTTGTCAGCACACA[-/C]AAAGTGATTATCATA | 69736 |
rs241814759 | in-del | -/T | | | intron-variant | Nup37 | Mm_Celera | 10:88176277 | TTTATTATCAGAGAA[-/T]TTTTTTTTCCCTCAG | 69736 |
rs241861383 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88165484 | GAAAGAAGACCTCAT[C/T]GTACCTGAATGCCCC | 69736 |
rs241911286 | in-del | -/GA | | | intron-variant | Nup37 | Mm_Celera | 10:88169822 | TTATCTTGTTCCTGT[-/GA]GAGGAGTCTGTGCTT | 69736 |
rs241975208 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88160271 | ACATGTTTTCTGTTA[A/G]TAGTAAGTAGCTCTC | 69736 |
rs242235622 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88151117 | AAAAATGTTTTTGAT[A/C]TTTATTTCTCAGCAT | 69736 |
rs242278406 | in-del | -/G | | | intron-variant | Nup37 | Mm_Celera | 10:88169666 | AAAAGGAACTGGGGA[-/G]GGGGGGGGAGGCTTA | 69736 |
rs242366300 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88168020 | TCCTATGCCAACACA[C/T]ACTTTGTGGGATCTT | 69736 |
rs242427491 | snp | A/C/T | | | downstream-variant-500B | Nup37 | GRCm38.p3 | 10:88178655 | GGCATCAGGTTCCTT[A/C/T]GGGAAAGTCCAGTCT | 69736 |
rs242546329 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88157437 | GGGCTTGTTATTTGT[A/G]GTGGAGGAAGTAGCT | 69736 |
rs242613374 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88149406 | CTTTCTCCAATGTGG[A/G]CCACTTACGTGTTGA | 69736 |
rs242879044 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88159046 | CCATTGGATTAGCCA[A/G]GAATTTTTTAGAGGA | 69736 |
rs242920026 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88149915 | GGAGAGCTGAGTTTC[A/C]TCACTCTGCCCTTGG | 69736 |
rs242931964 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88170270 | CTTAGTACTAAGATT[A/T]TGTAACAGTTGGGAA | 69736 |
rs243082209 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88160078 | GAAAACTAAATGTAC[A/T]CCCTGTGTTACAACT | 69736 |
rs243108387 | in-del | -/CAAA | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145368 | GTGCCAAATACTTTC[-/CAAA]CATTTAATATTAATT | 69736 |
rs243109480 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88155163 | TCCAGATTTTAGCTC[A/G]TACAGCTGTAGCTTC | 69736 |
rs243216880 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88147389 | GACTTAATCTGAAAA[A/G]ACTCAGCAGATAACT | 69736 |
rs243241792 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88171801 | CCTGATTAATGTGTG[C/T]GCCACCACGCCCAGC | 69736 |
rs243694724 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88162104 | CTGGGTCTGGCAGGC[C/T]ACAGCCAAGGCACAC | 69736 |
rs243754193 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88153005 | CTGATTTGGAGGCAT[G/T]CATTACCATTCAAAG | 69736 |
rs243830144 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88152475 | GATCCTTGTATACCT[A/G]TTAACTAATCTGAGA | 69736 |
rs243860644 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88153941 | TATGAGTATACTGTC[A/G]CTGTCCTCAGACACA | 69736 |
rs244150675 | snp | C/T | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145273 | GCAAATACTCGGTTG[C/T]TATTGTACAGTGACT | 69736 |
rs244182211 | in-del | -/C | | | intron-variant | Nup37 | Mm_Celera | 10:88156354 | TCAGAGACACACTTA[-/C]ATCATTCTTCACTAC | 69736 |
rs244247096 | in-del | -/C | | | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88148665 | GTATTAGATACACTT[-/C]AGATTTCCCCACATC | 69736 |
rs244321502 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88175783 | AGGTTATTATGAAAT[A/T]ATCCAAATTTCAGAG | 69736 |
rs244433419 | in-del | -/GCGCGC | | | intron-variant | Nup37 | Mm_Celera | 10:88154663 | TGTGTGTGTGTGTGT[-/GCGCGC]GTGCGTGCACATGTG | 69736 |
rs244466352 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88164646 | TATACATGTATTTAG[A/C]GCTTTTTTCCATAGC | 69736 |
rs244470373 | snp | C/G | | | intron-variant | Nup37 | Mm_Celera | 10:88164994 | CACAATCGAGGTGGC[C/G]ATGCCTTAACCACAT | 69736 |
rs244646752 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88173701 | TTCCCTCTTGTAAAT[A/T]ATTAAAAACAAACTC | 69736 |
rs244696985 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88147955 | CTCTTGCATATGACA[A/G]TGTCAGTACAACTTT | 69736 |
rs244764483 | in-del | -/T | | | intron-variant | Nup37 | Mm_Celera | 10:88173370 | AGTTCAGATCCTAGA[-/T]TTTTAACTTTTATAT | 69736 |
rs244841195 | in-del | -/ACTC | | | intron-variant | Nup37 | Mm_Celera | 10:88159465 | TTCAAGTAGATTATT[-/ACTC]ACCATCTCTTCAAAG | 69736 |
rs244844945 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88149263 | TTCTGCTATTATGGT[A/G]TACCAAAATAATATT | 69736 |
rs244848836 | snp | C/G | | | intron-variant | Nup37 | Mm_Celera | 10:88156008 | GGTTAATGTGGCCCA[C/G]ACTGACCTTGATCTC | 69736 |
rs244959526 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88149716 | AACAAGAGGCTTTTT[C/T]CTTTTATGAGCACAT | 69736 |
rs244964640 | in-del | -/T | | | intron-variant | Nup37 | Mm_Celera | 10:88170730 | ACGCTAGCCCAATAC[-/T]TTATTATGGAAATGG | 69736 |
rs245082143 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88167014 | TTAACTCAGTGAGCA[A/G]ATTAATGCTAATGAA | 69736 |
rs245206481 | in-del | -/T | | | intron-variant | Nup37 | Mm_Celera | 10:88169366 | ACCTAATTTAGGGTG[-/T]TTTTTTTTTAAGTTT | 69736 |
rs245378289 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88170976 | ATATCAAATTTGACA[A/G]TCTTTACTTTTTAGA | 69736 |
rs245522860 | in-del | -/AGAT | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146254 | GGATATGAACAAAAC[-/AGAT]AGAAGGTGTCAGAGG | 69736 |
rs245703651 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88168330 | TTTTCTTTGACAATG[G/T]CACTGTGTTATCCCG | 69736 |
rs245721282 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88149592 | AGAAAAAGGAAAGAT[A/G]AAGAAGGCAGACAAC | 69736 |
rs245809983 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88169493 | TTCCATCTTGGTAAG[C/T]GTACAACAATTGTAC | 69736 |
rs245821493 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88169290 | ATAAATATTGCAGTA[G/T]AAACAGCATAGTTAA | 69736 |
rs245871784 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88160166 | GTATAGCATCCATCT[G/T]CCTCATAAGGTTGTG | 69736 |
rs246087249 | snp | C/G | | | intron-variant | Nup37 | Mm_Celera | 10:88160720 | AAGTGACTGACTTCT[C/G]ACCTCAATAGCCTTT | 69736 |
rs246210674 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88176335 | GTCATCTGTCAGGCG[A/T]CCACCAGCACTTGCT | 69736 |
rs246243333 | in-del | -/A | | | intron-variant | Nup37 | Mm_Celera | 10:88156543 | TTTGTAAGCTGCCTC[-/A]AATCAATTTTGGAAC | 69736 |
rs246367319 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88177016 | ACAGGAGTGGCCTGT[A/C]TTAGACCGTTGTTGT | 69736 |
rs246375547 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88150954 | ATAAAGGTTATCGTA[G/T]ACTTTGTCTTATGTT | 69736 |
rs246441535 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88167220 | ATTTGAAAATCTGAC[A/C]TATATTGACATACCC | 69736 |
rs246479803 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88166140 | TACTCTTAGTTTAAG[A/G]CCAATGTATATGAGA | 69736 |
rs246581303 | in-del | -/C | | | intron-variant | Nup37 | Mm_Celera | 10:88154078 | GGGCCATTTCTCCAG[-/C]CCGTGCTTCTTATTC | 69736 |
rs246583681 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88162810 | TTGTTTTGTGCTAGC[A/G]TCTGCTGCTGGGCCT | 69736 |
rs246736709 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88165019 | CCACATGCGTGTTGT[C/T]TAGCCCAGAGGCCTC | 69736 |
rs246771235 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88163799 | TTTCTCTCTGGAGAC[G/T]TCTCTATATATATTC | 69736 |
rs246778072 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88153475 | ATGAAGTTCGGAGTA[C/T]TTTATTGTTTGTCTT | 69736 |
rs246836873 | snp | C/G | | | intron-variant | Nup37 | Mm_Celera | 10:88154515 | ACCAGTAACTCCTCT[C/G]CAGGGGGATCCGATG | 69736 |
rs246960757 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88155054 | GCTCTTTCTAACAGG[C/T]GTGAGCGTTCTGAGC | 69736 |
rs246994292 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88175707 | GGCACCCTCACACAG[A/G]CAGACATGCAGGCAA | 69736 |
rs247161774 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88165738 | ACCTGAGGGCTAGAG[A/G]CGAAACTCTGGTCCT | 69736 |
rs247230013 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146820 | TGCCCACTGGAACTG[A/C]GACCCGGGGGCACAG | 69736 |
rs247497149 | in-del | -/ATG | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145442 | GTCTGGTTTTGACAC[-/ATG]ATGAAGAAAATAATG | 69736 |
rs247585493 | in-del | -/A | | | intron-variant | Nup37 | GRCm38.p3 | 10:88160673 | TTAAAGGCGCACTAG[-/A]AAAAAAAAGACTGAG | 69736 |
rs247609412 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88162216 | TATATTTGCTTCTTT[A/G]CTTTAACTTTTTTTA | 69736 |
rs247621218 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88177621 | GATTTTTATTTTACA[C/T]GTATGGGTGTTTTGC | 69736 |
rs247632317 | in-del | -/AAG | | | upstream-variant-2KB, cds-indel, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146653 | GATCTAACGGACTAA[-/AAG]AAGATTTTGATGGGT | 69736 |
rs247641991 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88173210 | TAAATGTTTATCAAT[A/G]GATAAAGGAAATGTA | 69736 |
rs247643343 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88161232 | AGCACATATACACCA[G/T]TGGATCAAAGTCTCC | 69736 |
rs248289458 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88168976 | AGTAGGGCAAAGCTT[C/T]TTTTCTTAGCTTATT | 69736 |
rs248641297 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88168205 | CCATGTTACAGCTAA[A/G]TCTTCAGGATGGTAT | 69736 |
rs248680288 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88167366 | TGTCTTCAAGATTTT[A/T]TAAGTTTAATTCCCA | 69736 |
rs248757461 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88157980 | GGGGTGACAAACGTG[A/G]TCTAGCTTGGTGGCT | 69736 |
rs248815063 | in-del | -/A | | | intron-variant | Nup37 | Mm_Celera | 10:88158816 | AGAGGACTTGGATTT[-/A]CAAAGGCTATACATA | 69736 |
rs248887276 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88154162 | TTGCCACCAAGCCTT[A/T]CTACCTAAGTTCACT | 69736 |
rs248918694 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88153354 | AGCTACATCTCAAGT[C/T]CCCAATATGCTTTTT | 69736 |
rs248937347 | in-del | -/ATA | | | intron-variant | Nup37 | Mm_Celera | 10:88173878 | AAAGCATATTCATGG[-/ATA]ATAATAGCTATTAAT | 69736 |
rs249260436 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88151497 | ATTATTCAGAGAGGT[G/T]TTTTTTGTTTTTTAA | 69736 |
rs249327489 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88176626 | GACAGCTACAGTGTA[C/T]TCATATAAAATAAAT | 69736 |
rs249334889 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88163540 | TAGTACGCAGAGTTC[C/T]TTACAGTTCCAGGAA | 69736 |
rs249413566 | in-del | -/TTT | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146005 | AGTTTGCCTGAAATA[-/TTT]TTTTTTTCCATCAAC | 69736 |
rs249733702 | in-del | -/AT | | | intron-variant | Nup37 | Mm_Celera | 10:88169088 | CACTACCATAATAAA[-/AT]ATTACAGTATAAGCC | 69736 |
rs249774502 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88161544 | ACCATACTTAGTAAT[A/G]TACATACATCTATAC | 69736 |
rs249776511 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88150706 | AGGATAACGTGAAAG[G/T]AGGGCCAGGGAGATG | 69736 |
rs249840200 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88154287 | AATGTGGAGACAATA[C/T]AGTGCTACTTTGTTA | 69736 |
rs249862665 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88176976 | CATGGAAAGTCACAG[A/G]GGATCGTGGAGTTGC | 69736 |
rs249967549 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88165994 | TACTTTGGGGGATAC[A/C]AAAGAAGTAGACTCA | 69736 |
rs249986270 | in-del | -/TCC | | | intron-variant | Nup37 | Mm_Celera | 10:88170472 | AGACCACAATATACT[-/TCC]TAGTTAACTGACTTA | 69736 |
rs249988252 | in-del | -/A | | | intron-variant | Nup37 | Mm_Celera | 10:88169666 | CAAAAGGAACTGGGG[-/A]GGGGGGGGAGGCTTA | 69736 |
rs250017179 | in-del | -/AGATCCTCCTTAAGATAATAGATTC | | | intron-variant | Nup37 | Mm_Celera | 10:88160075 | TAGAAAACTAAATGT[-/AGATCCTCCTTAAGATAATAGATTC]ACTCCCTGTGTTACA | 69736 |
rs250077766 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88149836 | ACAAAGGAAGAGATC[A/G]AATCTGTTCTTCCGT | 69736 |
rs250088015 | in-del | -/TTTT | | | intron-variant | Nup37 | Mm_Celera | 10:88156516 | TGGTTTTTTTTCTTG[-/TTTT]TTTTTTTTTTTGTAA | 69736 |
rs250179616 | in-del | -/C | | | intron-variant | Nup37 | Mm_Celera | 10:88178069 | TTAAAAAGAAAAAAA[-/C]AATAGTTTTCTTTAT | 69736 |
rs250342341 | in-del | -/AGTTATATA | | | intron-variant | Nup37 | GRCm38.p3 | 10:88163590 | TATCCATCGTCAGTG[-/AGTTATATA]AGTGTTGTCATCAGC | 69736 |
rs250416294 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88176924 | AACAGTAATGCAGAG[A/C]AAGAAAGTATTCATA | 69736 |
rs250421550 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88172213 | ACAATTGCATTTGAG[C/T]TTTATAGAAATAAAT | 69736 |
rs250470408 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88168261 | TTATGGATTAAAGGT[A/G]TTGAAGTGGGAATCC | 69736 |
rs250501571 | snp | C/G | | | intron-variant | Nup37 | Mm_Celera | 10:88171407 | TTGAGATGAAGAGCC[C/G]TATTTGTGAGTAAGT | 69736 |
rs250625813 | snp | A/C | | | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88148140 | TGACAAACACTTTGT[A/C]AATTTTGTTTGTGAT | 69736 |
rs250672031 | in-del | -/AGAAGGC | | | intron-variant | Nup37 | Mm_Celera | 10:88149594 | AAAAAGGAAAGATGA[-/AGAAGGC]AGACAACAAGGAGAG | 69736 |
rs251007011 | in-del | -/CT | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145605 | TATGGAATCAGTCCC[-/CT]CTCTACTTCCAGTCT | 69736 |
rs251009233 | snp | A/T | | | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88147845 | ATGTAGGCCCAACAC[A/T]TGCTAAATCTTTTAA | 69736 |
rs251111512 | snp | C/T | | | downstream-variant-500B | Nup37 | Mm_Celera | 10:88178826 | AATGTAAACTATCTG[C/T]AGCTGGCAAAAATCA | 69736 |
rs251119077 | snp | G/T | | | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88148610 | CGTAGAGGTGTATTC[G/T]GATAAAGTCCAACAT | 69736 |
rs251184907 | in-del | -/AT | | | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88147350 | CCGGTCCCGCGTAAC[-/AT]GTGTCCAGTCTCTCT | 69736 |
rs251271101 | snp | A/G | | | downstream-variant-500B | Nup37 | Mm_Celera | 10:88178690 | TTATCAAGCTATCCA[A/G]TTTCTTCTCCCTTTG | 69736 |
rs251483177 | in-del | -/A | | | intron-variant | Nup37 | Mm_Celera | 10:88164296 | AGACAGCAAGTGTAC[-/A]ATTTTTTTTTTAACA | 69736 |
rs251530093 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88167665 | TCCCTTCTGTTCTCC[C/T]GTACTTAGTTAATCA | 69736 |
rs251598188 | in-del | -/T | | | intron-variant | Nup37 | GRCm38.p3 | 10:88149808 | TCTGCTTCAGCGGTG[-/T]TTGGGGGGCATGACA | 69736 |
rs251608469 | snp | C/T | | | downstream-variant-500B | Nup37 | Mm_Celera | 10:88178636 | CTACTTCCTGCTGAT[C/T]AGGGGCATCAGGTTC | 69736 |
rs251608578 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88166506 | GTTGTTTGCTTTGGG[A/G]TTTTTGGTTGGTTGG | 69736 |
rs251714756 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88162527 | CCATGAAAACCCAAA[A/G]CTAGAAACATTAATA | 69736 |
rs251747319 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88154414 | GAAAGCATTTTTTAA[A/T]AAATTGGTTTTGAGA | 69736 |
rs251774021 | in-del | -/TTTTT | | | intron-variant | Nup37 | GRCm38.p3 | 10:88156515 | TGGTTTTTTTTCTTG[-/TTTTT]TTTTTTTTTTTTTTT | 69736 |
rs252312751 | snp | A/T | | | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88148390 | TTCAGGTTAGTCCAC[A/T]AACTATACGGAGTGA | 69736 |
rs252350765 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88156512 | GTTTTGGTTTTTTTT[C/T]TTGTTTTTTTTTTTT | 69736 |
rs252376793 | in-del | -/A | | | intron-variant | Nup37 | Mm_Celera | 10:88165331 | TACAAAACTTATGAC[-/A]AAAAAATTAAAACCT | 69736 |
rs252488758 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88174290 | ATACGTGTGTGATAT[A/G]TGTTTATTTTTCTTT | 69736 |
rs252557011 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88172655 | ACCTCTGACATCCTC[A/G]TGTTTTTTCATTTCA | 69736 |
rs252560434 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88164094 | AGAACAACAGTCAGT[A/G]CTCTTACCCACTGAG | 69736 |
rs252607558 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88162714 | ATATATGTATATAAT[A/G]CTTAAACAAAACATG | 69736 |
rs252627769 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88175608 | GGTTAAAGGCCCTGG[A/T]TACTCTTCTAGATGA | 69736 |
rs252632003 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88161839 | TTATAGGCTATTATG[C/T]CTGTGTATTACCTGC | 69736 |
rs252659936 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88154062 | CATGCTCTTAACCGC[C/T]GGGCCATTTCTCCAG | 69736 |
rs252713066 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88165197 | AGAATTGATAAATTT[G/T]TATCTAGTAAAAGAA | 69736 |
rs252761060 | in-del | -/G | | | intron-variant | Nup37 | Mm_Celera | 10:88177306 | CTGCTTAAACCAAAA[-/G]GGTTTTTTTCTTTTA | 69736 |
rs252827780 | in-del | -/AAA | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145938 | TCCTATTTATCTCTT[-/AAA]AAACAAAATTGAAGA | 69736 |
rs252931237 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88173417 | GAGGCTTAGGTCAAC[A/G]GGGGTCATCCCTCTT | 69736 |
rs253165306 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88162398 | ACGATAACAATCCTG[A/G]ATAGGACAAGTCAGA | 69736 |
rs253543232 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88157377 | GACTTAGAGAGTGAA[A/G]CACAGTGATTACCAG | 69736 |
rs253732727 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88171045 | TAGTCCTAAAGAAGT[C/T]AAGAACTATAAAACC | 69736 |
rs253763831 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88160008 | CAGTGACCTTGCTGC[A/G]GTTATCATTTACTGT | 69736 |
rs253795933 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88169893 | TTCAAAAACAGGAAA[A/G]GAAGTGTGACTTCAT | 69736 |
rs253892093 | in-del | -/TTT | | | intron-variant | Nup37 | GRCm38.p3 | 10:88177217 | GGTTTTCAAATTGGA[-/TTT]TTTTTTTTTTTTACT | 69736 |
rs253949706 | in-del | -/ACA | | | intron-variant | Nup37 | GRCm38.p3 | 10:88149227 | AGGCTCAACACCACC[-/ACA]CCATCTTCCCAGAGT | 69736 |
rs253992078 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88176050 | GAGCTCACTGGCCTG[C/T]CAGCCCATAAGGAAT | 69736 |
rs254157965 | snp | A/C | | | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88147237 | TGGGAATATTGACCC[A/C]GGGCTTTAAAGACCT | 69736 |
rs254165168 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88165074 | ACCTTTCTACAGTTC[A/T]TTTGTTTTTCTTACA | 69736 |
rs254201532 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88176174 | AGCCCCTAAAACTGA[A/G]CACTTGCAGAACACA | 69736 |
rs254242902 | in-del | -/AT | | | intron-variant | Nup37 | Mm_Celera | 10:88170888 | GTCTTTTCTGATAAA[-/AT]ATATGATTCTAATAT | 69736 |
rs254593868 | snp | A/G | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145283 | GGTTGCTATTGTACA[A/G]TGACTATGGTTTTTG | 69736 |
rs254612582 | in-del | -/CG | | | intron-variant, upstream-variant-2KB | Nup37, Parpbp | GRCm38.p3 | 10:88147926 | GACTATTGGTAGTAC[-/CG]GCGTTTATGGTACTC | 69736 |
rs254915324 | in-del | -/CACA | | | intron-variant | Nup37 | Mm_Celera | 10:88154542 | GATGCCTCTGGCTTC[-/CACA]CACACCTACACAAAC | 69736 |
rs255004478 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88167516 | AAAGAATAGTCCACT[A/G]CTTTCTGTAATCAGC | 69736 |
rs255028139 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88166205 | TGAAATATTATAGAT[C/T]GTATGTTCTGGTTAG | 69736 |
rs255028187 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88154921 | ATAACACACGGCTTT[A/G]CTCTGATGTCCCCCA | 69736 |
rs255040542 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88159170 | AAGAGGCTGGGAACC[A/C]TGGACTGTTCTGTCT | 69736 |
rs255064033 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88165382 | TTGGTCAATTGGGAG[A/G]CTGGGGTTGAAACCT | 69736 |
rs255066547 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88169675 | CTGGGGAGGGGGGGG[A/G]GGCTTATATCTCTTA | 69736 |
rs255151419 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88155657 | CTGTGGTTACCCTGG[G/T]CTGCTGTGCCTGGAC | 69736 |
rs255429864 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88170058 | TCTGAAGACAGCTAC[A/G]GTGTACTTACATCAA | 69736 |
rs255554408 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88148183 | GACAGGCAATAAACA[A/G]CTATTTGATTCTTAC | 69736 |
rs255834362 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88151372 | GACAGAACTGGGGCA[G/T]TGAATACACTTGACA | 69736 |
rs255851433 | in-del | -/A | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145078 | CTGAAGAAAGCATGC[-/A]AAAGAGAAGTAAGGT | 69736 |
rs255889281 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88161043 | AAAAATTAAGTCATT[A/G]TAGCTTCTGTATAGC | 69736 |
rs255959343 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88159113 | ATTTATTATATGACT[A/G]ACACAATAGGAGCTG | 69736 |
rs256011949 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88169434 | TCTTTCCTGTTCATA[G/T]TTTTTCAGTTTATAT | 69736 |
rs256073796 | in-del | -/TTTT | | | intron-variant | Nup37 | Mm_Celera | 10:88153892 | CTCTACTTCTTATTC[-/TTTT]TTTTTTTTTAAGATT | 69736 |
rs256114874 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88160075 | TTAGAAAACTAAATG[C/T]ACTCCCTGTGTTACA | 69736 |
rs256115695 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88149641 | GAGAAGAATGTTTGT[A/G]TCATTCAAACGCTTG | 69736 |
rs256163884 | snp | C/G | | | intron-variant | Nup37 | Mm_Celera | 10:88175018 | GCCTCCTCTTCGGTG[C/G]AGTTTGGGGATTGCT | 69736 |
rs256220062 | in-del | -/A | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145486 | AGCTAGTAAATAGCC[-/A]AAAAAGCATAAATTC | 69736 |
rs256276892 | snp | C/G | | | intron-variant | Nup37 | Mm_Celera | 10:88164012 | ACCAGAAGAGGGCAT[C/G]AGATCCCATTACAGA | 69736 |
rs256497753 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88163670 | ATGGAGACGGGGAGT[A/G]AGAAGGGGTCTAAGG | 69736 |
rs256618172 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88154019 | GTGGTTGCTGGGAAT[C/T]GAACTCAGGACCTCT | 69736 |
rs256792832 | snp | G/T | | | intron-variant | Nup37 | GRCm38.p3 | 10:88166292 | ATTTTATATATTTTT[G/T]TAACTTTGGTATATG | 69736 |
rs257213344 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88168620 | GGGGCTCTGACCCAA[A/G]CCCTTAGACATGGTA | 69736 |
rs257219749 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88155451 | GCCGGGCGTGGTGGC[G/T]CACGCCTTTAATCCC | 69736 |
rs257247408 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146496 | AAGGAAATAGCCAAC[C/T]TCCTTATTGCCAGCA | 69736 |
rs257250131 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88154963 | ACCCTACTCCCTGCA[C/T]AGCAGCTTTGATAGA | 69736 |
rs257297124 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88148487 | TACAAGAAAAAAAAA[-/T]TTTTTGAAGATCTAC | 69736 |
rs257359193 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88147022 | AGCGGGCGCACGCCC[C/T]GGCCACCTATGGTCG | 69736 |
rs257373818 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88164996 | CAATCGAGGTGGCGA[A/T]GCCTTAACCACATGC | 69736 |
rs257374337 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88158778 | TGGCAAGGTTGGATG[A/G]CTGAGAGGCAAAGGC | 69736 |
rs257375787 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88176844 | TGCCTGTGTCTCCCA[C/T]CTGTAGAGACCATGT | 69736 |
rs257473136 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88176009 | GCCCTACCCCAGCAC[G/T]GGGGAGTGCAGACAG | 69736 |
rs257489844 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88177777 | GGGTCCTCTGAAAGT[G/T]CTCTGAAAGACCCAG | 69736 |
rs257513085 | in-del | -/TTTT | | | intron-variant | Nup37 | Mm_Celera | 10:88152218 | AAAACCTGGCAGTGG[-/TTTT]TTTTTTTTTTTTTCA | 69736 |
rs257526133 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88177006 | CTGCTTTTGCACAGG[A/G]GTGGCCTGTCTTAGA | 69736 |
rs257558298 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88165783 | AGCGCTCTCGCTGGG[A/G]AACTGCCTCTGCAGC | 69736 |
rs257751810 | in-del | -/CTGTAACTTC | | | intron-variant | Nup37 | Mm_Celera | 10:88155007 | GCTGAGCTCTGCCTA[-/CTGTAACTTC]ATCCGTGGAATCACA | 69736 |
rs257797258 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88160721 | AGTGACTGACTTCTC[A/G]CCTCAATAGCCTTTC | 69736 |
rs258000617 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88158314 | CAAAGTGAGCTCTGT[A/G]TGTGGCTGAGGTGCA | 69736 |
rs258035201 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88153045 | CATACTTAAAACACG[C/T]GTATGTGCTCAGTTA | 69736 |
rs258052270 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88150092 | TGGGTTTCAGCAGGA[C/T]GGTTTTCAGACTCTT | 69736 |
rs258181911 | in-del | -/GTATTTCAT | | | intron-variant | Nup37 | Mm_Celera | 10:88174035 | TATGCATTTGGTTAC[-/GTATTTCAT]ATATTTCATAACAAT | 69736 |
rs258652012 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88154896 | GTGTAGTTTTATAGT[C/T]CATACTCTTATAACA | 69736 |
rs258663789 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88173051 | TTCTCATAGGTCCCC[C/T]TTTGAGTTTCATGGT | 69736 |
rs258669920 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88171483 | TGCTTCTCTAGTCCA[C/T]CTTTAATCTGGCAAC | 69736 |
rs258671290 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88160231 | GAACAATATTTTATA[C/T]ATAGTAGCATATATA | 69736 |
rs258734014 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88171689 | AAAATAGAAAGGCTG[G/T]TGTGGGGAGAGAGGG | 69736 |
rs258772874 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88170593 | TCAGTTTTATATAAT[A/G]ACCAACAAAAATCAA | 69736 |
rs258805815 | in-del | -/TTTTAAATGGCTC | | | intron-variant | Nup37 | Mm_Celera | 10:88150907 | AAAAGGCAGAATGAA[-/TTTTAAATGGCTC]TTTTAAGTAGAGTAC | 69736 |
rs258848255 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88152679 | TGCCAAGAAAAACAC[G/T]GCCAAATGCTCTTCT | 69736 |
rs258869306 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88160821 | TGGAGTGAAACTATT[C/T]GGTAGGGACATTGTA | 69736 |
rs259114651 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88157322 | GTTCCAAATACAAAC[A/T]GTTGAGTTGGCACCA | 69736 |
rs259252147 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88148638 | CATAACTGAGCACAC[A/G]TGTATTTCTATGTAT | 69736 |
rs259318834 | in-del | -/AA | | | intron-variant | Nup37 | Mm_Celera | 10:88150295 | AGACCAAATAAGGAT[-/AA]AAAGTTTCAAACCTT | 69736 |
rs259516542 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146618 | CTGAGAAGCCTGCAC[C/T]CGTCGTGTGCCAGAT | 69736 |
rs259523517 | in-del | -/CCACTCTTT | | | intron-variant | Nup37 | Mm_Celera | 10:88173766 | GTTTCTGACCAGTCC[-/CCACTCTTT]CCACTCTGTCACTGC | 69736 |
rs259566499 | in-del | -/CG | | | intron-variant | Nup37 | GRCm38.p3 | 10:88150856 | TGTATATAGCACACA[-/CG]CGCGCACACACACAC | 69736 |
rs259741519 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88149906 | GTTGATCCTGGAGAG[C/T]TGAGTTTCCTCACTC | 69736 |
rs259771283 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88177824 | AATTTAGGGGCTAAC[A/T]AGGAGTCCACTGCTT | 69736 |
rs259849054 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88168129 | CCTGAAATGATTTCA[G/T]CAAGACCCTATAAAA | 69736 |
rs259932430 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88177053 | GACGGTGCTTACTGT[A/T]ATGCTTTCCTCTCTC | 69736 |
rs259941417 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88167255 | CAAACTTCTTGCTTC[A/C]GATTATCATTACATT | 69736 |
rs260000238 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88155059 | TTCTAACAGGCGTGA[A/G]CGTTCTGAGCCTCAA | 69736 |
rs260015882 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88157827 | GACTGAGAGTTGTCA[C/T]ACTGTCCATCAACTC | 69736 |
rs260018143 | in-del | -/GAGG | | | intron-variant | Nup37 | Mm_Celera | 10:88159821 | ATACTCGGGGTGCTA[-/GAGG]GAGGGAGGCAGGGCA | 69736 |
rs260089921 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88165873 | ATCCTATTCCTAGTC[A/G]GTGGCAAATCACAGA | 69736 |
rs260123183 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88158798 | GAGGCAAAGGCGGCA[C/T]AGGAGAGGACTTGGA | 69736 |
rs260161925 | snp | C/G | | | intron-variant | Nup37 | Mm_Celera | 10:88156224 | GTGCCTAGACAACAG[C/G]AAGTAGTAGAAAATC | 69736 |
rs260232072 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88151627 | CAGTGGGTGTGGTGG[A/C]AAGGCCTGCTACTTC | 69736 |
rs260271949 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88173826 | TGCACCTGAATGAAA[C/T]AAACATTCTCAGAAA | 69736 |
rs260648420 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88176522 | GAGCACTGACTGTTC[C/T]AGAGGTCCTGAGTTC | 69736 |
rs260761590 | snp | A/C | | | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88147755 | AAATTAGAATGTTAA[A/C]GGTCATATAATTCGA | 69736 |
rs260895389 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88163314 | AGTATTTGATTTTCC[A/G]CTGGGTACATGGACT | 69736 |
rs260965777 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88162291 | GGTTTCCCCTTCACC[C/T]AGCTCCTCAGAGCTC | 69736 |
rs260983573 | snp | A/G | | | downstream-variant-500B | Nup37 | Mm_Celera | 10:88178657 | CATCAGGTTCCTTAG[A/G]GAAAGTCCAGTCTTC | 69736 |
rs261024742 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88164387 | TTGGGTAGAACCTTG[A/T]CCTGAAATTACCATT | 69736 |
rs261107888 | in-del | -/AC | | | intron-variant | Nup37 | GRCm38.p3 | 10:88149978 | TTTGGGTGCTGTTGA[-/AC]ATTCATTCCCGTTCT | 69736 |
rs261111132 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88167936 | CGCAGGAAATTCCCT[C/T]TTGAGTTCTCAAACA | 69736 |
rs261308067 | snp | C/T | | | downstream-variant-500B | Nup37 | Mm_Celera | 10:88178842 | AGCTGGCAAAAATCA[C/T]GTCTGTCTTAGTTAG | 69736 |
rs261395157 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88168222 | CTTCAGGATGGTATT[A/G]GTGTGGGAATTCCTT | 69736 |
rs261461873 | in-del | -/T | | | intron-variant | Nup37 | Mm_Celera | 10:88168697 | CAGTCTCTACCACGG[-/T]TTTTTGGGGTTTTTT | 69736 |
rs261467171 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88162772 | GTGTGGGCCGGGAGC[A/C]GACTTCCAAAAACAC | 69736 |
rs261746418 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88165552 | CTCAAGAGCAAAGCT[A/C]TTTCTTCAGTCACAT | 69736 |
rs261808239 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88162024 | ATTTTTCTAGTAAGA[A/C]GTATTTAGAATAATG | 69736 |
rs261884884 | snp | C/G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88157164 | TTGCGGGGGGGGGGG[C/G/T]GATGGGGGGTGAGGG | 69736 |
rs261954274 | in-del | -/GT | | | intron-variant | Nup37 | Mm_Celera | 10:88149815 | AGCGGTGTTTGGGGG[-/GT]GCATGACAAAGGAAG | 69736 |
rs261955295 | in-del | -/AC | | | intron-variant | Nup37 | Mm_Celera | 10:88159663 | AGCCTAGGCTGGGTT[-/AC]AGAGTGGTGGTGGGC | 69736 |
rs262168163 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88169768 | CATGGAGGAATGGTG[C/T]TTACTGCCTTGCTCT | 69736 |
rs262179259 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88164687 | GTCCTGAAGGTCCTA[A/G]TGTTTGTTGAGATAT | 69736 |
rs262232357 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88159925 | CACAGAGAAACCCTG[A/T]CTTGGAAAACCAAAA | 69736 |
rs262398437 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88167187 | TAATACTCAGTTCCA[A/G]TGCTAACTTCAGAGT | 69736 |
rs262485207 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88156285 | AGGGCTTCCCTGACC[C/T]ACTCACTGCATCAGA | 69736 |
rs262520566 | in-del | -/TT | | | intron-variant | Nup37 | Mm_Celera | 10:88174161 | TAATAATAGCCACTC[-/TT]TTCTTGATTTAAGAG | 69736 |
rs262569595 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88151467 | TCTCCCAAAACAACT[A/G]CTTTTCTCATTGGAA | 69736 |
rs262823478 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88150950 | TAATATAAAGGTTAT[C/T]GTAGACTTTGTCTTA | 69736 |
rs262842913 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88154228 | TAGCAAGTCATCCTG[A/T]CTCCACACAGCACCG | 69736 |
rs262987140 | in-del | -/CACACACGCGCGCA | | | intron-variant | Nup37 | GRCm38.p3 | 10:88150850 | GTGTACTGTATATAG[-/CACACACGCGCGCA]CACACACACACACAC | 69736 |
rs263020411 | in-del | -/T | | | intron-variant | Nup37 | Mm_Celera | 10:88164733 | TCCTGCCGCTAGTGC[-/T]ATCTTAGATTATCAT | 69736 |
rs263066504 | in-del | -/TATATATACCAA | | | intron-variant | Nup37 | Mm_Celera | 10:88173390 | ACTTTTATATTGGTG[-/TATATATACCAA]TATATATACAGGAGG | 69736 |
rs263085414 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88156010 | TTAATGTGGCCCACA[A/C]TGACCTTGATCTCTC | 69736 |
rs263088601 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88162835 | GGGCCTGGGACCTGC[C/T]TTTGATTTGTATGCA | 69736 |
rs263217792 | snp | C/G | | | intron-variant | Nup37 | Mm_Celera | 10:88149404 | AACTTTCTCCAATGT[C/G]GACCACTTACGTGTT | 69736 |
rs263372045 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88155040 | GACGGACGGAATGTG[C/T]TCTTTCTAACAGGCG | 69736 |
rs263422781 | in-del | -/C | | | intron-variant | Nup37 | Mm_Celera | 10:88173506 | GCTCCCAAATTACCA[-/C]CAATGCATTAGAGAA | 69736 |
rs263544536 | in-del | -/CTGTAGGCTA | | | downstream-variant-500B | Nup37 | Mm_Celera | 10:88178614 | CTGGGGTGTAGATCT[-/CTGTAGGCTA]CTTCCTGCTGATTAG | 69736 |
rs263793248 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88153190 | TCGCCTAGGTGAAGG[A/G]CACCATGTTACTGCT | 69736 |
rs263950062 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88175759 | AGTTATATATTAAAA[A/T]TTTTCTATAGGTTAT | 69736 |
rs264147028 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime | Nup37, Parpbp | Mm_Celera | 10:88146930 | GGCAGAGGTTTGAAT[A/C]GCCTCGGCGTCCCTT | 69736 |
rs264231273 | snp | A/G | | | synonymous-codon | Nup37 | Mm_Celera | 10:88174442 | TCTAATGGCTCAGCA[A/G]GCAATTTTATCTCTT | 69736 |
rs264341360 | snp | A/C | | | intron-variant | Nup37 | GRCm38.p3 | 10:88149227 | AAGGCTCAACACCAC[A/C]CCATCTTCCCAGAGT | 69736 |
rs264415673 | in-del | -/AA | | | intron-variant | Nup37 | Mm_Celera | 10:88165330 | TACAAAACTTATGAC[-/AA]AAAAAAATTAAAACC | 69736 |
rs264442659 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88168436 | AGCATTTACATATGT[A/T]CACATGTCCATTTCA | 69736 |
rs264620897 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88148147 | CACTTTGTAAATTTT[A/G]TTTGTGATCCACAGT | 69736 |
rs264655410 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88169010 | CCATTGATAACCATT[A/G]GAGCATTCGTGCTCT | 69736 |
rs264773634 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88171553 | TCAGACAGATGAGAA[A/C]TTGTATAAGATAGGA | 69736 |
rs264815312 | snp | C/G | | | intron-variant | Nup37 | Mm_Celera | 10:88160991 | TTGCTTGTGTTCCAG[C/G]CACATTTTTCTTTTC | 69736 |
rs264899887 | snp | A/T | | | intron-variant | Nup37 | Mm_Celera | 10:88174610 | ACATAAATATGTTGT[A/T]AAATGACCCATATAG | 69736 |
rs264929433 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88163549 | GAGTTCTTTACAGTT[C/T]CAGGAAGGGGGACAA | 69736 |
rs265108044 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88157679 | TCTTTCCAGAGATCA[A/G]TATCCCTTGCTTTAA | 69736 |
rs265130996 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88168039 | TTGTGGGATCTTTTA[A/G]TTAATTAATTATATG | 69736 |
rs265291335 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88160079 | AAAACTAAATGTACT[C/T]CCTGTGTTACAACTC | 69736 |
rs265371372 | in-del | -/A | | | utr-variant-3-prime | Nup37 | Mm_Celera | 10:88178389 | GATAAAGACTACATG[-/A]AAAATATGTTCCTAT | 69736 |
rs265412618 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88162109 | TCTGGCAGGCCACAG[C/T]CAAGGCACACAGCAT | 69736 |
rs265436479 | in-del | -/TGCT | | | intron-variant | Nup37 | Mm_Celera | 10:88174965 | CTGGAGTTGTGTGGA[-/TGCT]TGCTTTGGTAGGGTT | 69736 |
rs265456123 | snp | A/C | | | intron-variant | Nup37 | Mm_Celera | 10:88152505 | AATTAGGAGTTTAGC[A/C]ATTTTGGAAGACTCC | 69736 |
rs265586693 | in-del | -/A | | | intron-variant | Nup37 | Mm_Celera | 10:88150296 | AGACCAAATAAGGAT[-/A]AAGTTTCAAACCTTA | 69736 |
rs265635251 | snp | A/G | | | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88148021 | TAATCTTAGGACTCT[A/G]TTTGTATTAAATTTA | 69736 |
rs265718547 | snp | G/T | | | downstream-variant-500B | Nup37 | Mm_Celera | 10:88178770 | GCAGGCCCTCTCAGG[G/T]CTCTCAATTTTATAC | 69736 |
rs265991593 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88173233 | GAAATGTATATGTAC[A/G]CACACAATTGGATTT | 69736 |
rs266122378 | snp | A/G | | | intron-variant | Nup37 | Mm_Celera | 10:88176072 | ATAAGGAATGGTGAC[A/G]CTGTGACTCAGTGAG | 69736 |
rs266174385 | snp | G/T | | | intron-variant | Nup37 | Mm_Celera | 10:88166714 | GACTCTTAGGATCTG[G/T]CATTAAGATGGAGTT | 69736 |
rs266198086 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88177659 | TATGTATGTGCACCA[C/T]ATGAATGCCTGGTGC | 69736 |
rs386846049 | in-del | -/T | | | intron-variant | Nup37 | Mm_Celera | 10:88175132 | AGGACATGTATTTTT[-/T]CAACCACTTAGAAAA | 69736 |
rs386851011 | snp | C/T | | | intron-variant | Nup37 | GRCm38.p3 | 10:88152803 | CTTTACATTATGATT[C/T]CTAACAGTAGCAAGA | 69736 |
rs386862939 | snp | C/T | | | intron-variant | Nup37 | Mm_Celera | 10:88156283 | GCAGGGCTTCCCTGA[C/T]CCACTCACTGCATCA | 69736 |
rs386866313 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88148492 | GAAAAAAAAATTTTT[-/T]GAAGATCTACAGGGA | 69736 |
rs386885905 | in-del | -/T | | | intron-variant | Nup37 | Mm_Celera | 10:88177491 | TCATACCCATTTTTT[-/T]ATAGATAGCTTAGAT | 69736 |
rs386900216 | snp | A/G | | | intron-variant | Nup37 | GRCm38.p3 | 10:88164624 | TGTGTGTGTGTGTGT[A/G]TGTGTGTATACATGT | 69736 |
rs386936995 | in-del | -/TT | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146013 | TGAAATATTTTTTTT[-/TT]CCATCAACCATTTAA | 69736 |
rs386955580 | in-del | -/CAGA | | | intron-variant | Nup37 | Mm_Celera | 10:88171716 | AGGGAGAGACAGAGA[-/CAGA]GACAGAGACAGAGAA | 69736 |
rs387007275 | snp | C/G | | | intron-variant | Nup37 | GRCm38.p3 | 10:88157662 | AGACTTTGTAAGTCT[C/G]ATCTTTCCAGAGATC | 69736 |
rs387029452 | in-del | -/T | | | intron-variant | Nup37 | Mm_Celera | 10:88152791 | AAATCACAGATACTT[-/T]ACATTATGATTTCTA | 69736 |
rs387034266 | in-del | -/TATATAAGT | | | intron-variant | Nup37 | Mm_Celera | 10:88163593 | CCATCGTCAGTGAGT[-/TATATAAGT]GTTGTCATCAGCAAC | 69736 |
rs387067783 | snp | C/T | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | GRCm38.p3 | 10:88145405 | TTCCATCTCCTGTGT[C/T]CTGATGATGTCAGTC | 69736 |
rs387104484 | snp | A/C | | | downstream-variant-500B | Nup37 | Mm_Celera | 10:88178494 | CCTAATCCCTTCTAA[A/C]CCCCCCACTCCCCGC | 69736 |
rs387116688 | snp | C/T | | | intron-variant | Nup37 | GRCm38.p3 | 10:88171809 | ATGTGTGTGCCACCA[C/T]GCCCAGCGTAAAACT | 69736 |
rs387144450 | in-del | -/A | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145491 | GTAAATAGCCAAAAA[-/A]GCATAAATTCAAGAT | 69736 |
rs387165837 | in-del | -/T | | | intron-variant | Nup37 | Mm_Celera | 10:88170732 | GCTAGCCCAATACTT[-/T]ATTATGGAAATGGCA | 69736 |
rs387172276 | in-del | -/T | | | intron-variant | Nup37 | Mm_Celera | 10:88168845 | CAGTAGGTTTTTTTT[-/T]GTTTTGTTTTGTTTT | 69736 |
rs387208451 | in-del | -/T | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146218 | TACCTCCCAGCCTGT[-/T]GTGAAGACTCGATGA | 69736 |
rs387249296 | snp | C/T | | | intron-variant | Nup37 | GRCm38.p3 | 10:88178012 | TAATTATTTCATCAA[C/T]ACTTATCAGCACTTA | 69736 |
rs387267518 | in-del | -/T | | | intron-variant | Nup37 | Mm_Celera | 10:88168839 | CTAGACCAGTAGGTT[-/T]TTTTTTGTTTTGTTT | 69736 |
rs387274793 | snp | A/G | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | GRCm38.p3 | 10:88145394 | TAATTACTTTGTTCC[A/G]TCTCCTGTGTCCTGA | 69736 |
rs387279352 | snp | A/G/T | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | GRCm38.p3 | 10:88146231 | GTTGTGAAGACTCGA[A/G/T]GAGACGCTGGATATG | 69736 |
rs387279922 | snp | G/T | | | intron-variant | Nup37 | GRCm38.p3 | 10:88160327 | TTTCGTATAAGAATA[G/T]TATTAACCCTCATAA | 69736 |
rs387303462 | in-del | -/T | | | intron-variant | Nup37 | Mm_Celera | 10:88176285 | CAGAGAATTTTTTTT[-/T]CCCTCAGGCCTTCTT | 69736 |
rs387308476 | in-del | -/TTTTT | | | intron-variant | Nup37 | GRCm38.p3 | 10:88172845 | TTTTCCTTTTTTTTT[-/TTTTT]GTTGTTCTAGCTTTC | 69736 |
rs387316697 | in-del | -/TG | | | intron-variant | Nup37 | Mm_Celera | 10:88149816 | GCGGTGTTTGGGGGG[-/TG]CATGACAAAGGAAGA | 69736 |
rs387331620 | in-del | -/A | | | utr-variant-3-prime | Nup37 | Mm_Celera | 10:88178393 | AAGACTACATGAAAA[-/A]TATGTTCCTATTGTG | 69736 |
rs387333974 | snp | A/C | | | intron-variant | Nup37 | GRCm38.p3 | 10:88155582 | CTCGAAAAACCAAAA[A/C]ATAAACAAACAAACA | 69736 |
rs387346081 | snp | A/G | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | GRCm38.p3 | 10:88145401 | TTTGTTCCATCTCCT[A/G]TGTCCTGATGATGTC | 69736 |
rs387355241 | snp | A/T | | | intron-variant | Nup37 | GRCm38.p3 | 10:88178072 | AAAAAGAAAAAAAAA[A/T]AGTTTTCTTTATTTT | 69736 |
rs387387793 | in-del | -/TGTG | | | intron-variant | Nup37 | Mm_Celera | 10:88154666 | GTGTGTGTGTGTGTG[-/TGTG]CGTGCACATGTGCAT | 69736 |
rs387419670 | in-del | -/TTTG | | | intron-variant | Nup37 | Mm_Celera | 10:88168575 | GTTTTTGTTTGTTTG[-/TTTG]CTTGTTTGTTTTCCC | 69736 |
rs387424957 | in-del | -/AG | | | intron-variant | Nup37 | Mm_Celera | 10:88151299 | ATGTTCACCTAACAG[-/AG]CTTCCCCTGGCAAGG | 69736 |
rs387451292 | snp | A/C | | | intron-variant | Nup37 | GRCm38.p3 | 10:88176732 | TAGATTTAATCTCAG[A/C]ACACACATGGCAGCT | 69736 |
rs387458763 | in-del | -/TAAA | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88146257 | TATGAACAAAACAGA[-/TAAA]AGGTGTCAGAGGGAA | 69736 |
rs387494142 | snp | C/T | | | intron-variant | Nup37 | GRCm38.p3 | 10:88156970 | CCTGTCTCGAAAACC[C/T]AAATAAATAAATAAA | 69736 |
rs387545421 | in-del | -/AATA | | | intron-variant | Nup37 | Mm_Celera | 10:88169281 | ATAAATAAATAAATA[-/AATA]TTGCAGTATAAACAG | 69736 |
rs387548670 | in-del | -/AT | | | intron-variant | Nup37 | Mm_Celera | 10:88170892 | TTTCTGATAAAATAT[-/AT]GATTCTAATATTAAA | 69736 |
rs387625632 | in-del | -/GGAC | | | intron-variant, upstream-variant-2KB | Nup37, Parpbp | Mm_Celera | 10:88148659 | TCTATGTATTAGATA[-/GGAC]CACTTCAGATTTCCC | 69736 |
rs387640515 | snp | A/T | | | intron-variant | Nup37 | GRCm38.p3 | 10:88169330 | GAGAGGAAGTTAATA[A/T]CTGATTAATTTTTCT | 69736 |
rs387661119 | in-del | -/AAA | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145941 | TATTTATCTCTTAAA[-/AAA]CAAAATTGAAGAAGA | 69736 |
rs387678763 | in-del | -/T | | | intron-variant | Nup37 | GRCm38.p3 | 10:88168707 | CCACGGTTTTTGGGG[-/T]TTTTTTTTTTAATAT | 69736 |
rs387699614 | in-del | -/GATCCTCCTTAAGATAATAGATTCA | | | intron-variant | Nup37 | Mm_Celera | 10:88160076 | AGAAAACTAAATGTA[-/GATCCTCCTTAAGATAATAGATTCA]CTCCCTGTGTTACAA | 69736 |
rs387707231 | in-del | -/AT | | | downstream-variant-500B | Nup37 | Mm_Celera | 10:88178428 | TGTACTTTTTGAGCT[-/AT]GTTTGGTTTTGTTTT | 69736 |
rs387746951 | in-del | -/A | | | intron-variant | Nup37 | Mm_Celera | 10:88173918 | GCATACTTGGAAAAA[-/A]TCTTGTTCGTTATAG | 69736 |
rs387752994 | snp | C/T | | | downstream-variant-500B | Nup37 | GRCm38.p3 | 10:88178518 | TCCCCGCCTCATCCC[C/T]TCCTTCCCCCCCCCC | 69736 |
rs387760250 | in-del | -/TTT | | | intron-variant | Nup37 | Mm_Celera | 10:88152232 | GTTTTTTTTTTTTTT[-/TTT]CAGTTCACTTCTTTG | 69736 |
rs387786514 | in-del | -/G | | | intron-variant | Nup37 | Mm_Celera | 10:88177308 | GCTTAAACCAAAAGG[-/G]TTTTTTTCTTTTAAT | 69736 |
rs387824243 | in-del | -/A | | | intron-variant | Nup37 | Mm_Celera | 10:88150298 | ACCAAATAAGGATAA[-/A]GTTTCAAACCTTATT | 69736 |
rs387845373 | snp | A/G | | | intron-variant | Nup37 | GRCm38.p3 | 10:88172823 | TATTTCTAAATGTTT[A/G]GATATATTTTCCTTT | 69736 |
rs387875984 | in-del | -/CCT | | | intron-variant | Nup37 | Mm_Celera | 10:88170473 | GACCACAATATACTT[-/CCT]AGTTAACTGACTTAT | 69736 |
rs387891227 | in-del | -/AACA | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | Mm_Celera | 10:88145370 | GCCAAATACTTTCCA[-/AACA]TTTAATATTAATTAC | 69736 |
rs387896024 | snp | C/T | | | intron-variant | Nup37 | GRCm38.p3 | 10:88177213 | TACTTGGTTTTCAAA[C/T]TGGATTTTTTTTTTT | 69736 |
rs387899625 | in-del | -/T | | | intron-variant | Nup37 | Mm_Celera | 10:88168717 | TGGGGTTTTTTTTTT[-/T]AATATTATTAACACA | 69736 |
rs578374275 | snp | A/G | | | intron-variant | Nup37 | GRCm38.p3 | 10:88162144 | GGCTGCTCTCAGAAG[A/G]GCTTTTTCCCTTTTT | 69736 |
rs578607776 | snp | C/T | | | missense | Nup37 | GRCm38.p3 | 10:88172021 | TGGAAGGAAAGCAGA[C/T]AGCTCATTTTCTTCT | 69736 |
rs578817573 | snp | G/T | | | intron-variant | Nup37 | GRCm38.p3 | 10:88162675 | TATGTAATAAATATT[G/T]TTTAATAATTAATTT | 69736 |
rs578972356 | snp | A/G | | | intron-variant | Nup37 | GRCm38.p3 | 10:88173927 | GGAAAAATCTTGTTC[A/G]TTATAGATGATATTC | 69736 |
rs579373856 | snp | A/G | | | intron-variant | Nup37 | GRCm38.p3 | 10:88169730 | TCAGGTTAAGAATTC[A/G]GGTTGGAAACAAAAA | 69736 |
rs579472458 | snp | A/G | | | intron-variant | Nup37 | GRCm38.p3 | 10:88165342 | TGACAAAAAAATTAA[A/G]ACCTAGGTATGGCAT | 69736 |
rs579690042 | snp | A/G | | | intron-variant | Nup37 | GRCm38.p3 | 10:88168685 | ACTACAGGGTTCTCA[A/G]TCTCTACCACGGTTT | 69736 |
rs579717469 | snp | A/G | | | intron-variant | Nup37 | GRCm38.p3 | 10:88156549 | AGCTGCCTCAAATCA[A/G]TTTTGGAACTTACAT | 69736 |
rs580408743 | snp | G/T | | | intron-variant | Nup37 | GRCm38.p3 | 10:88164593 | ATGTGTGTGTGTGTG[G/T]GTGTGTGTGTGTGTG | 69736 |
rs580472244 | snp | G/T | | | intron-variant | Nup37 | GRCm38.p3 | 10:88176589 | ATAATGGGATCCAAT[G/T]CCCTCCTCCGGAGTG | 69736 |
rs580605947 | snp | A/G | | | intron-variant | Nup37 | GRCm38.p3 | 10:88170718 | AGTGATAAGAATTAC[A/G]CTAGCCCAATACTTA | 69736 |
rs580750724 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nup37, Parpbp | GRCm38.p3 | 10:88147363 | ACATGTGTCCAGTCT[C/T]TCTGAGATGGGACTT | 69736 |
rs580847348 | snp | A/G | | | intron-variant | Nup37 | GRCm38.p3 | 10:88159667 | CTAGGCTGGGTTAGA[A/G]TGGTGGTGGGCGGAG | 69736 |
rs581076646 | snp | A/G | | | intron-variant | Nup37 | GRCm38.p3 | 10:88168786 | TTTCTAGTTCTCAAT[A/G]TCTTTTTTTTATAAG | 69736 |
rs581477141 | snp | A/T | | | intron-variant | Nup37 | GRCm38.p3 | 10:88169243 | CCTGTCTCAAATTAA[A/T]TAAATAAATAAATAA | 69736 |
rs581748645 | snp | G/T | | | downstream-variant-500B | Nup37 | GRCm38.p3 | 10:88178435 | TTTGAGCTATGTTTG[G/T]TTTTGTTTTTTTTAA | 69736 |
rs581860820 | snp | A/G | | | intron-variant | Nup37 | GRCm38.p3 | 10:88156305 | ACTGCATCAGACCCC[A/G]GGCAGTGTGGGGCTT | 69736 |
rs582025527 | snp | C/T | | | intron-variant | Nup37 | GRCm38.p3 | 10:88162441 | AAGGGAAAATAAGAG[C/T]TGAAAAAAAAAAAAA | 69736 |
rs582094633 | snp | A/G | | | intron-variant | Nup37 | GRCm38.p3 | 10:88156867 | TTAATCCCAGCACTC[A/G]GGAGGCAGAGGCAGG | 69736 |
rs582292662 | snp | A/G | | | intron-variant | Nup37 | GRCm38.p3 | 10:88158812 | ACAGGAGAGGACTTG[A/G]ATTTCAAAGGCTATA | 69736 |
rs582463361 | snp | A/C | | | intron-variant | Nup37 | GRCm38.p3 | 10:88163376 | GTGTCAGGTGCGGGT[A/C]TCGTCTTTTGAAGTG | 69736 |
rs582659326 | snp | A/G | | | intron-variant | Nup37 | GRCm38.p3 | 10:88175113 | TCTTTTGCTTTAGGT[A/G]AGCAGGACATGTATT | 69736 |
rs582858871 | snp | C/T | | | intron-variant | Nup37 | GRCm38.p3 | 10:88161864 | ACCTGCTAAATTTTT[C/T]TTGTGAGGGACATGA | 69736 |
rs583432813 | snp | A/G | | | intron-variant | Nup37 | GRCm38.p3 | 10:88177671 | CCATATGAATGCCTG[A/G]TGCTTTCGGGGTCAG | 69736 |
rs583582651 | snp | C/G | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | GRCm38.p3 | 10:88145063 | AAGCCCGGGTAAGGT[C/G]CTGAAGAAAGCATGC | 69736 |
rs583614583 | snp | A/G | | | intron-variant | Nup37 | GRCm38.p3 | 10:88168846 | AGTAGGTTTTTTTTT[A/G]TTTTGTTTTGTTTTT | 69736 |
rs583738976 | snp | C/T | | | intron-variant | Nup37 | GRCm38.p3 | 10:88157092 | ACAGAGAAACCCTGT[C/T]TCGAAAACCCAAATA | 69736 |
rs583935813 | snp | C/T | | | downstream-variant-500B | Nup37 | GRCm38.p3 | 10:88178631 | GTAGGCTACTTCCTG[C/T]TGATTAGGGGCATCA | 69736 |
rs584229795 | snp | A/T | | | intron-variant | Nup37 | GRCm38.p3 | 10:88161865 | CCTGCTAAATTTTTC[A/T]TGTGAGGGACATGAA | 69736 |
rs584317005 | snp | C/T | | | intron-variant | Nup37 | GRCm38.p3 | 10:88159807 | CACCTTTCATCCCAA[C/T]ACTCGGGGTGCTAGA | 69736 |
rs584432500 | snp | C/T | | | intron-variant, upstream-variant-2KB | Nup37, Parpbp | GRCm38.p3 | 10:88147364 | CATGTGTCCAGTCTC[C/T]CTGAGATGGGACTTA | 69736 |
rs584722707 | snp | A/G | | | intron-variant | Nup37 | GRCm38.p3 | 10:88151152 | TTCTAATTACAAGGA[A/G]ATGTATTCGGAAACA | 69736 |
rs585190489 | snp | A/C | | | intron-variant | Nup37 | GRCm38.p3 | 10:88155235 | ATTTCTCTTAAGAGT[A/C]TAATTGCTGGGTCAC | 69736 |
rs585355286 | snp | A/T | | | intron-variant | Nup37 | GRCm38.p3 | 10:88162644 | ATTATATAATTATAT[A/T]TTTTAAATTTATAAA | 69736 |
rs585357327 | snp | C/T | | | intron-variant | Nup37 | GRCm38.p3 | 10:88164633 | GTGTGTATGTGTGTA[C/T]ACATGTATTTAGAGC | 69736 |
rs585627148 | snp | A/C | | | intron-variant | Nup37 | GRCm38.p3 | 10:88156364 | CACTTAATCATTCTT[A/C]ACTACTTGTTTATCC | 69736 |
rs585858089 | snp | A/G | | | intron-variant | Nup37 | GRCm38.p3 | 10:88156939 | TTCCAGGACAGCCAC[A/G]GCTATACAGAGAAAC | 69736 |
rs585914633 | snp | A/T | | | intron-variant | Nup37 | GRCm38.p3 | 10:88173863 | ACTTTACACAGTAGA[A/T]AAAGCATATTCATGG | 69736 |
rs585939267 | snp | A/C | | | intron-variant | Nup37 | GRCm38.p3 | 10:88176582 | ACCATCTATAATGGG[A/C]TCCAATGCCCTCCTC | 69736 |
rs586105453 | snp | C/T | | | intron-variant | Nup37 | GRCm38.p3 | 10:88164292 | TTAGGAGACAGCAAG[C/T]GTACATTTTTTTTTT | 69736 |
rs586672291 | snp | A/G | | | intron-variant | Nup37 | GRCm38.p3 | 10:88159279 | CAAAGAACAGGGACA[A/G]CAGCCACAGCAGGCT | 69736 |
rs586864530 | snp | A/G | | | intron-variant | Nup37 | GRCm38.p3 | 10:88150842 | TTCAGCATGTGTACT[A/G]TATATAGCACACACG | 69736 |
rs587024020 | snp | C/T | | | intron-variant | Nup37 | GRCm38.p3 | 10:88159845 | AGGCAGGGCAGAGGC[C/T]AGTGGGTCTCTGAGT | 69736 |
rs587360203 | snp | A/G | | | intron-variant | Nup37 | GRCm38.p3 | 10:88169196 | TGGTCTATAGAGTGA[A/G]TTCCAGAACAGCCAG | 69736 |
rs587387621 | snp | C/T | | | intron-variant | Nup37 | GRCm38.p3 | 10:88157152 | ATAAAGCCTTATTTG[C/T]GGGGGGGGGGGTGAT | 69736 |
rs864275233 | snp | A/G | | | upstream-variant-2KB, intron-variant | Nup37, Parpbp | GRCm38.p3 | 10:88146172 | TAAGAATGGTCACAA[A/G]GCAATCAGGACTATG | 69736 |