SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3701420 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Nup153 | Mm_Celera | 13:46724835 | CCTCCAAAAAAAGTA[C/G]AAAGTAGTTGAGTAG | 218210 |
rs29230657 | snp | A/G | 0.255 | 0.24995 | intron-variant | Nup153 | Mm_Celera | 13:46681253 | TTGACCTGTGAAAAA[A/G]TAAAAACATTACAAT | 218210 |
rs29232895 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nup153 | Mm_Celera | 13:46722059 | TAAATCTAGCACTCC[C/T]AGCACTCAAGAGGCT | 218210 |
rs29238438 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Nup153 | Mm_Celera | 13:46714465 | TTTTTAAAAAATGGT[G/T]AAGAGCAACTGAAAA | 218210 |
rs29238895 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nup153 | Mm_Celera | 13:46713520 | ACGCCCTTAATCCTA[A/G]TATTTAACAGGCTGA | 218210 |
rs29240509 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nup153 | Mm_Celera | 13:46726997 | GGCCTGTTGCCACAT[C/T]TTTCCCTTGTTCCCT | 218210 |
rs29249703 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nup153 | Mm_Celera | 13:46687897 | CAGAAAGGATAGATG[A/G]GGTGATTGACACCGT | 218210 |
rs29250511 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Nup153 | Mm_Celera | 13:46717014 | GATTTATATATTACT[C/T]GGTCAGATGCTATCA | 218210 |
rs29251962 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Nup153 | Mm_Celera | 13:46728983 | GGCTGGTGACAGACA[C/T]CTTTGATCCCAGCAC | 218210 |
rs29512269 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nup153 | Mm_Celera | 13:46725625 | AATTAAATCTGCTAA[C/T]CAAAAAAGAGTTATC | 218210 |
rs29512674 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Nup153 | Mm_Celera | 13:46708204 | CAACTTTAGGTAAGA[G/T]GAATTTTGAACATGG | 218210 |
rs29530311 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Nup153 | Mm_Celera | 13:46729173 | GTTTTTTTGTTTTTT[A/G]TTTTTATGAAATAAG | 218210 |
rs29531550 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Nup153 | Mm_Celera | 13:46682975 | ACTGTAAGTATAGAT[A/G]TCAACTATCATACAA | 218210 |
rs29535034 | snp | A/C | 0.375 | 0.216506 | intron-variant | Nup153 | Mm_Celera | 13:46706490 | CATCATCATCATCAT[A/C]ATAATAATAATAATT | 218210 |
rs29554257 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Nup153 | Mm_Celera | 13:46724051 | ATCTGGAATGAATAA[A/C]ATATTGAGAAATATT | 218210 |
rs29589536 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Nup153 | Mm_Celera | 13:46700453 | ATATAAAGATGATAT[A/G]TTAGTGGAAGTTTAC | 218210 |
rs29612110 | snp | A/T | 0.375 | 0.216506 | intron-variant | Nup153 | Mm_Celera | 13:46717974 | AAAAAAATCTGAAGA[A/T]TTAGCTTCATCTTGG | 218210 |
rs29630521 | snp | A/G | 0.290657 | 0.246672 | upstream-variant-2KB | Nup153 | Mm_Celera | 13:46728591 | GCTTCACTACTTACA[A/G]ACTTGACCTTGGATG | 218210 |
rs29665289 | snp | A/T | 0.401235 | 0.199068 | intron-variant | Nup153 | Mm_Celera | 13:46694567 | TTAATTGTTTGATGT[A/T]TATCTCCGCCATCTC | 218210 |
rs29725571 | snp | A/G | 0.387812 | 0.208586 | downstream-variant-500B | Nup153 | Mm_Celera | 13:46679418 | TTGGACATAGAAAAT[A/G]GTGAAGGACTGGCCG | 218210 |
rs29909320 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nup153 | Mm_Celera | 13:46711427 | TACTGTGACATCGAG[C/T]TATACATAGGATATC | 218210 |
rs36241320 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nup153 | Mm_Celera | 13:46709548 | TCCCTTTTTCAAACA[C/T]GTTCCCTAGTGACTG | 218210 |
rs36251853 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46687723 | ACAGTCATACTTTTT[A/T]AAAAAAATCTAAGTC | 218210 |
rs36255088 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46693218 | AGAAAGGCTGAACCA[C/T]TGCAAGCTTTCAGCA | 218210 |
rs36255719 | snp | A/T | 0.32 | 0.24 | intron-variant | Nup153 | Mm_Celera | 13:46704467 | AATAAATAATTTTTT[A/T]AAAAGTGAGTTTTTA | 218210 |
rs36255773 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Nup153 | Mm_Celera | 13:46708657 | AGACATGAACTGGTG[G/T]TTTGCTAATAGTCCT | 218210 |
rs36263873 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46685409 | TTCTACAGGTGATAA[A/G]ATTTCATGATCAAAG | 218210 |
rs36267311 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Nup153 | Mm_Celera | 13:46683834 | GCTGGCAATTCAGCA[A/G]AACCAATCCAACTAC | 218210 |
rs36276499 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nup153 | Mm_Celera | 13:46715584 | GGCCCCATCTGGCTG[A/G]CCAGGAAGCACAATG | 218210 |
rs36302384 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Nup153 | Mm_Celera | 13:46695436 | CCCTGGGAGCCACTG[A/C]AGGGTTCTTTTCCTT | 218210 |
rs36390778 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46699345 | TATATCACTAATCTG[C/T]TGAATCCAGCATAAT | 218210 |
rs36399517 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Nup153 | Mm_Celera | 13:46684871 | ACAAAAGAAATGTTT[G/T]CCCCCAGGAATGAGG | 218210 |
rs36430418 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nup153 | Mm_Celera | 13:46688495 | TCTTGAAGGCTAATT[C/T]CGTTCAGAGATTTCT | 218210 |
rs36430476 | snp | A/T | 0.32 | 0.24 | intron-variant | Nup153 | Mm_Celera | 13:46703941 | GTAAACAAGATGCAA[A/T]TAAAGTCCCATGTCA | 218210 |
rs36442541 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46690872 | AACAATCTCTGCATT[G/T]TAAGTATGTTCTCTT | 218210 |
rs36450894 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46704344 | AGTGTTAATCATATG[C/T]ACAATTGAGAAATAG | 218210 |
rs36458149 | snp | A/C | 0.124444 | 0.216185 | upstream-variant-2KB | Nup153 | Mm_Celera | 13:46728557 | GTTGTCAACACACAC[A/C]GTGCTGGCATTCTGA | 218210 |
rs36501003 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46698575 | CCTTTCTGTGGTCTA[C/T]GGTTCTTACTGTTTA | 218210 |
rs36506032 | snp | C/G | 0.124444 | 0.216185 | missense | Nup153 | Mm_Celera | 13:46687142 | CCTCTTTCTTTTCTT[C/G]TTGCCCAAGAGTAGA | 218210 |
rs36557980 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Nup153 | Mm_Celera | 13:46708131 | TCCATGGCTTTTCAC[A/T]CACAAGAACATTTAT | 218210 |
rs36573426 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nup153 | Mm_Celera | 13:46701247 | TTAAAAATCACTTTG[A/G]TTTAAAACAAAACAT | 218210 |
rs36586064 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46682166 | CCACAGCAGAATACA[C/T]GACCAACAGAAAATC | 218210 |
rs36606239 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nup153 | Mm_Celera | 13:46700804 | TTACACAGAAGAGAA[C/T]GCACACACACATTAT | 218210 |
rs36606610 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nup153 | GRCm38.p3 | 13:46683857 | CCAACTACAAACCCC[A/G]TTTTTCTCTCCTAGC | 218210 |
rs36636133 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Nup153 | Mm_Celera | 13:46708758 | TCATACCATGGATGG[G/T]CTTTACTCAGTCACA | 218210 |
rs36649423 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Nup153 | Mm_Celera | 13:46713923 | AAGAAAGGGCAGGGC[A/T]CTAGTACAATAAAAG | 218210 |
rs36671578 | snp | G/T | 0.231111 | 0.249285 | downstream-variant-500B | Nup153 | Mm_Celera | 13:46679798 | GGCCCATTAGTTCTA[G/T]AAACTGTTGGAGTGC | 218210 |
rs36672449 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Nup153 | Mm_Celera | 13:46682503 | TGTACACACCCAAAC[G/T]TCCACTCCTTCGTGT | 218210 |
rs36675879 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nup153 | Mm_Celera | 13:46708829 | GAGGCCTCTATAGCT[C/T]TCTCCTTCCCCAATG | 218210 |
rs36684919 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46682753 | ACAGCAGCCTAGAGT[A/G]AAACGGGGTTGATCA | 218210 |
rs36685178 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46693438 | AAAACACCAGGATTC[C/G]TCTTAGCCGTTTCAT | 218210 |
rs36687012 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Nup153 | Mm_Celera | 13:46693768 | TTCGGGCTTATTTTG[C/T]ACTAAACAGGTATCA | 218210 |
rs36707642 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46684635 | TTGAGTATTTGCTAA[C/T]TCCTGCTAATAATTA | 218210 |
rs36711211 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Nup153 | Mm_Celera | 13:46729213 | TTAGGAAAAAGAATC[A/G]ATTATGGAGAATCAT | 218210 |
rs36733382 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46715656 | GTGTTGCTGGTAACA[C/T]TGGAAAAAAAATATG | 218210 |
rs36761434 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46689977 | TGCCAAAATACAAGG[A/T]AGAGCCAATAAATAG | 218210 |
rs36811716 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46684675 | GTCACCTTGGTGGCA[C/T]CCTAAATCTCCTAAT | 218210 |
rs36843312 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46698191 | TGCATCACTTCCTAA[C/T]TCCACATTTTCAGTT | 218210 |
rs36849099 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Nup153 | GRCm38.p3 | 13:46681156 | TAACACCTTTGTGAC[C/T]TTTATTTCTTGCGTC | 218210 |
rs36890866 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nup153 | Mm_Celera | 13:46709012 | ATCCGGGTCTGAGGT[A/G]CTTTATAAATTAACA | 218210 |
rs36914756 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Nup153 | Mm_Celera | 13:46717484 | TAGATTTAGTGGTAG[C/G]TAGTACATGTTTTCA | 218210 |
rs36974474 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46700582 | ATTATTTAGAGATGA[C/T]TTAAATATAATATGA | 218210 |
rs37013426 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nup153 | Mm_Celera | 13:46704376 | CAAAACCCTAAGGCA[A/G]TAACCAGAGAATCCA | 218210 |
rs37031517 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46687879 | TAGTCCACAATAACA[A/G]AACAGAAAGGATAGA | 218210 |
rs37032704 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46692981 | GTTAAGAGTTTTTCA[C/T]CAAAAATTAATTGTA | 218210 |
rs37039884 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46706286 | ATAAAATTTGTAGTT[C/T]TGTGCTGCACCAAGA | 218210 |
rs37041901 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46701573 | AAAGAATAAAAACAG[A/G]AATCACCTCACTTAT | 218210 |
rs37060076 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46684436 | TAAATTTAATGTAAA[A/G]TACACTGTCTCACAT | 218210 |
rs37112207 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46681891 | TTTCAGGCTAGCCAG[A/G]GCTGCCACAAAACAG | 218210 |
rs37136717 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Nup153 | Mm_Celera | 13:46710553 | CAAAACACCACAGCA[A/C]TGTCCTAAAGAAAAT | 218210 |
rs37165959 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46708546 | CTAAACACATGCAAA[A/T]TCTTCAAAGCAGTTT | 218210 |
rs37201133 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Nup153 | Mm_Celera | 13:46687654 | TACTGGGAGCAGTAG[G/T]CACTTCCCTATCCTG | 218210 |
rs37205662 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46682277 | ATGGATAGGCTGCCA[C/T]TCAGTGACTCACTCT | 218210 |
rs37211069 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46700121 | AATTATGAACAATAC[C/T]TTATAAATATATGAG | 218210 |
rs37220988 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46699509 | AATATACTATTATGA[C/T]CAGCTCACTGTAAAC | 218210 |
rs37224236 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Nup153 | Mm_Celera | 13:46708070 | ATTTTGCAGACAAAC[A/T]GACATTTTAGCCATG | 218210 |
rs37257019 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon | Nup153 | GRCm38.p3 | 13:46683941 | AGACACACTATTACT[A/G]CTGGCTCCTGTCCCA | 218210 |
rs37264163 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46686051 | CTATACCACTCTCAT[C/T]ATCTAAGTGAATTCA | 218210 |
rs37299108 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46699120 | TTCTTCTCCAGCCTC[A/G]TGACAAAGCATGTGC | 218210 |
rs37299474 | snp | C/T | 0.231111 | 0.249285 | missense | Nup153 | GRCm38.p3 | 13:46684006 | ACGTGGTGGCTGGCT[C/T]GCTCTCTTGAGGAAA | 218210 |
rs37327296 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46683778 | GCCCATTTTTCCACA[G/T]GTGAGACCTTAGACC | 218210 |
rs37370150 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46681763 | TCACTCTGACCTGGA[A/C]ATATTAAACGTGGGT | 218210 |
rs37381791 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46682830 | AAGCCATCAAATAAA[A/G]TTGACTAAAACTCTG | 218210 |
rs37385159 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Nup153 | Mm_Celera | 13:46715619 | CAACCTCCTTAGAGA[G/T]CTACCAGATAAAGCC | 218210 |
rs37387053 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46698253 | AATGTTTCAGGAACA[C/T]ATGCTTCTACAGATT | 218210 |
rs37422002 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46682211 | TCACTCAACTCAGTA[A/G]CATGCAAGACAGCAT | 218210 |
rs37422319 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Nup153 | Mm_Celera | 13:46716943 | CACACAAATATTTTT[A/T]AAAACTACTCAATAA | 218210 |
rs37469062 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Nup153 | Mm_Celera | 13:46686009 | TTTATATGCAGAAAA[G/T]CTTCCTCTAAATTTT | 218210 |
rs37476278 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nup153 | Mm_Celera | 13:46682316 | ACAAAAACATAAGAA[A/G]CAGGGTTGTATAATA | 218210 |
rs37503989 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nup153 | Mm_Celera | 13:46712264 | CAGGGAGTGACTATA[C/T]ACACTGATGGTGGGA | 218210 |
rs37516168 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46684553 | TATGTCATATTACAA[C/T]AGCAGCACCCTGACT | 218210 |
rs37527724 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Nup153 | Mm_Celera | 13:46708220 | GAATTTTGAACATGG[C/T]TAAAATTTATTTTTC | 218210 |
rs37540064 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46686034 | AATTTTCTAATGTTT[C/G]CCTATACCACTCTCA | 218210 |
rs37559114 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Nup153 | Mm_Celera | 13:46686747 | CTCATCTTTGGTTTG[C/T]TCTGAATTCCCAAAG | 218210 |
rs37562691 | snp | C/T | 0.375 | 0.216506 | downstream-variant-500B | Nup153 | Mm_Celera | 13:46679587 | ATAGTAAGAAAAATA[C/T]CTTTTCATAAGAACA | 218210 |
rs37620626 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46682149 | CTTTCCATTCAGTGA[C/T]CCCACAGCAGAATAC | 218210 |
rs37621820 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Nup153 | GRCm38.p3 | 13:46687263 | AACTTCTTCAGGTTT[A/G]GAATCAGATAACACT | 218210 |
rs37631768 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nup153 | Mm_Celera | 13:46715107 | AAATGGCCAGAACTA[C/T]GGCTCAGTGTTAGAG | 218210 |
rs37639135 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Nup153 | Mm_Celera | 13:46714947 | TGACTGCAGAATCAA[A/G]TAAATAAATGCCTTG | 218210 |
rs37650097 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nup153 | Mm_Celera | 13:46704900 | TATCTATACATCCAC[A/G]GGCACGTAAGCACAC | 218210 |