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 |