SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13479988 | snp | A/G | 0.416017 | 0.186918 | synonymous-codon, downstream-variant-500B, intron-variant | Wdr59 | GRCm38.p3 | 8:111460762 | ACACCATGAACTCAC[A/G]TAGCGGCTGTGGGAC | 319481 |
rs31302816 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr59 | Mm_Celera | 8:111453306 | TCAAACATGAATGGC[C/T]CAGCTCGCTATTTAA | 319481 |
rs31302819 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Wdr59 | GRCm38.p3 | 8:111453472 | AGAGACCTCGCTAAG[C/T]TGACCCCAGACGATG | 319481 |
rs31302821 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Wdr59 | Mm_Celera | 8:111453542 | AGCTCTGGGTTTCTT[A/G]TTGCGTGTGCTTGTT | 319481 |
rs31303834 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr59 | Mm_Celera | 8:111453940 | CTCAGATCCTGAATA[C/T]CTTCCCTCCTTTCTT | 319481 |
rs31303837 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Wdr59 | Mm_Celera | 8:111454233 | CTGGATTTCTCCACG[G/T]GCAGCTACTTCCTCC | 319481 |
rs31303839 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wdr59 | GRCm38.p3 | 8:111454271 | GATGGACTGACTCCT[C/T]GGTGCAGCTTACAGT | 319481 |
rs31303842 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr59 | Mm_Celera | 8:111454303 | ACTGCTCATGTTAAC[A/G]TTTTGTCTGAGTCTC | 319481 |
rs31303945 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr59 | Mm_Celera | 8:111461493 | ATTCTGTCAAGAGGC[A/G]TCTGTAAGCTAACTA | 319481 |
rs31303948 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Wdr59 | GRCm38.p3 | 8:111461549 | GAAGAGGCAATGGGA[A/G]CATCATCAGCTGCCC | 319481 |
rs31303950 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr59 | Mm_Celera | 8:111461586 | TAGCCTCGACCAGCA[A/G]AGAAGCAAGCTTCAA | 319481 |
rs31303952 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Wdr59 | GRCm38.p3 | 8:111461760 | TGCTTTTATGAGCTG[C/T]CTAACAGGATCCTAG | 319481 |
rs31304095 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Wdr59 | GRCm38.p3 | 8:111484333 | TCAGTCCCAAGGCCG[A/C]TGTGCTGAGCATGGG | 319481 |
rs31304098 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr59 | Mm_Celera | 8:111484382 | AGACCAGGCTCCCTT[C/T]GTGCAACACAGCAGC | 319481 |
rs31304101 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Wdr59 | GRCm38.p3 | 8:111484487 | GGAAACTGTATATGT[A/G]AGATGCTGTATTTCT | 319481 |
rs31304114 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Wdr59 | Mm_Celera | 8:111466226 | TAACACTTTCTGTGA[C/T]GTGTTCAAGGGCTTG | 319481 |
rs31304117 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Wdr59 | Mm_Celera | 8:111466271 | CAGCCTCTGCTCCTA[C/T]TGTCTTTCAATAAAA | 319481 |
rs31304120 | snp | A/C | 0.426035 | 0.177515 | intron-variant | Wdr59 | GRCm38.p3 | 8:111466292 | TTCAATAAAAGAAGG[A/C]TCTAAATTCAGCTTG | 319481 |
rs31304123 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr59 | GRCm38.p3 | 8:111466683 | CAATTTGTTAGTCAC[C/T]ATCAAGAAGCTACCA | 319481 |
rs31304406 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Wdr59 | Mm_Celera | 8:111471923 | TGTTGATGTGTTGCT[A/C]TAAACGTTCTTTATA | 319481 |
rs31304408 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Wdr59 | Mm_Celera | 8:111472428 | GTGATCCCTAAGTGT[G/T]TCCCCATTTGAAATA | 319481 |
rs31304411 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr59 | GRCm38.p3 | 8:111472797 | CTGATGGATTTATAG[A/G]TATATATGCTGCAAA | 319481 |
rs31304864 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr59 | Mm_Celera | 8:111454343 | CCTCTTGCTCCCTTT[C/T]TACAATCCTGTAATA | 319481 |
rs31304867 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Wdr59 | Mm_Celera | 8:111454546 | CACACCTAGCAATAA[A/T]AGTGTTTAGTATCAG | 319481 |
rs31304870 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr59 | Mm_Celera | 8:111454651 | TCTATTTCTCTGTGT[C/T]GCCTGCAGTCTCGCA | 319481 |
rs31304873 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr59 | Mm_Celera | 8:111454672 | CAGTCTCGCATGGTG[C/T]TTCAGAGCAGGAGAT | 319481 |
rs31304964 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Wdr59 | Mm_Celera | 8:111484550 | TGCAAGACCTCCTGA[A/T]CCCAGGTTAACGTTT | 319481 |
rs31304967 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Wdr59 | Mm_Celera | 8:111484958 | GAGTTAAAAATGAAG[A/C]CTGGAGCTAGAGAGA | 319481 |
rs31304970 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr59 | Mm_Celera | 8:111485251 | ATTGGAAATGTTTTA[A/G]AAATGTTTTAGTCAG | 319481 |
rs31304973 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr59 | Mm_Celera | 8:111485507 | GGTGTGCAGAGTAGG[C/T]GTCAATGCTGAAGTG | 319481 |
rs31305006 | snp | A/G | 0.459184 | 0.136902 | synonymous-codon, nc-transcript-variant | Wdr59 | GRCm38.p3 | 8:111466887 | TCGGTTGCCGGAGTC[A/G]GAGCCTTCCCGCTTA | 319481 |
rs31305009 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Wdr59 | GRCm38.p3 | 8:111466950 | ACCAGAAGTGACTAA[C/T]GGGGCCTCTGGAGAG | 319481 |
rs31305012 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Wdr59 | GRCm38.p3 | 8:111467050 | CGTGCCCCACAATTA[C/T]ATGAAATCAGCATCT | 319481 |
rs31305034 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Wdr59 | GRCm38.p3 | 8:111461859 | ATGACTGACACTTAC[C/T]ATCTCCAGAGCCCAA | 319481 |
rs31305037 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Wdr59 | GRCm38.p3 | 8:111461881 | AGAGCCCAAAGGCCC[A/G]TGTGCCCAGTGGTGT | 319481 |
rs31305039 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr59 | Mm_Celera | 8:111461949 | CATAAGGGTTTCAAA[C/T]TCTTGTGAGTGACAA | 319481 |
rs31305042 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr59 | Mm_Celera | 8:111462038 | CTAAAAGCAAAGGGC[C/T]TTCTTCCCTTCACAC | 319481 |
rs31305344 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Wdr59 | Mm_Celera | 8:111473006 | AGGGACTCTGGCAGG[C/G]CTAAGGTCCTGCTGC | 319481 |
rs31305347 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr59 | Mm_Celera | 8:111473494 | TCTTTAGGTCACTTA[C/T]ACTTAAGTTCTTAGT | 319481 |
rs31305350 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Wdr59 | Mm_Celera | 8:111473843 | CCTCAGGACGGACTC[A/G]TCGGCCTCCACAGCG | 319481 |
rs31305353 | snp | A/T | 0.46875 | 0.121031 | intron-variant | Wdr59 | GRCm38.p3 | 8:111473920 | TCCGTCAGCCTGCTC[A/T]GCTTAAAGAGACTAC | 319481 |
rs31305736 | snp | A/C | 0.387812 | 0.208586 | intron-variant | Wdr59 | GRCm38.p3 | 8:111454710 | AGGGTTTGGCTCATA[A/C]GTCAGCTCCATATCA | 319481 |
rs31305739 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr59 | Mm_Celera | 8:111454711 | GGGTTTGGCTCATAC[A/G]TCAGCTCCATATCAC | 319481 |
rs31305742 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr59 | Mm_Celera | 8:111455088 | TTTGTTCACTGTCTC[C/T]TCTCTAAAGACCACT | 319481 |
rs31305756 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr59 | Mm_Celera | 8:111485603 | CATAAGGATAAAGAT[A/G]TAGGGCTAGAGATGT | 319481 |
rs31305759 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr59 | Mm_Celera | 8:111486159 | TATTGTCTTTTTCCA[C/T]CATGATCAGAGTAAA | 319481 |
rs31305762 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Wdr59 | GRCm38.p3 | 8:111486370 | CAGTGCTGTAATCTT[C/T]GCCCAGCATTTCCCA | 319481 |
rs31305965 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr59 | Mm_Celera | 8:111467297 | GTTCAAAGTTCTTGC[C/T]TGAAACGATTCAAAG | 319481 |
rs31305968 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Wdr59 | Mm_Celera | 8:111467466 | CCTGAATTATTTCTA[C/T]AAGCGATCATTTCTG | 319481 |
rs31305971 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Wdr59 | Mm_Celera | 8:111467623 | AAGTCACAGAGTGTC[A/G]CCCCATCTGGCATCT | 319481 |
rs31305973 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Wdr59 | GRCm38.p3 | 8:111467827 | TTCTGCCTCAATATG[A/G]CCCTAGGCAAGCTAC | 319481 |
rs31305984 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr59 | Mm_Celera | 8:111462392 | ACGAGGATGCAAACG[A/G]CTCGGGCTGGCAGAA | 319481 |
rs31305987 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr59 | Mm_Celera | 8:111462457 | TGATGCATTAACAGG[A/G]TCCTCAGTGACTGAC | 319481 |
rs31305990 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Wdr59 | GRCm38.p3 | 8:111462696 | CATCATAGTCCAAGG[C/T]CCAGCTTCTTCAGCG | 319481 |
rs31305993 | snp | A/C | 0.426035 | 0.177515 | intron-variant | Wdr59 | GRCm38.p3 | 8:111462729 | CTTGGCCTCTTCTGA[A/C]GCTTCCCTGGTGAAC | 319481 |
rs31306018 | snp | C/T | 0.475309 | 0.108333 | downstream-variant-500B, upstream-variant-2KB | Wdr59, Mir1957b | Mm_Celera | 8:111448307 | TTTTGGAAGACAATG[C/T]TCTTACAGAAATAAT | 319481 |
rs31306021 | snp | C/G | 0.475309 | 0.108333 | downstream-variant-500B, upstream-variant-2KB | Wdr59, Mir1957b | GRCm38.p3 | 8:111448340 | ACACAAGAAAACTAT[C/G]TCATTCTAAACAGGG | 319481 |
rs31306126 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Wdr59 | Mm_Celera | 8:111473928 | CCTGCTCAGCTTAAA[C/G]AGACTACTGCATTAC | 319481 |
rs31306129 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr59 | Mm_Celera | 8:111474019 | ATCTGTTTTGGACAT[C/T]GTAAATACATTGAAC | 319481 |
rs31306132 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdr59 | Mm_Celera | 8:111474373 | CTGTGGAGAAGCAGC[A/G]TTCTAGGAGCTGGCC | 319481 |
rs31306575 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr59 | Mm_Celera | 8:111486910 | ATAATACCACTGAAT[A/G]CATACCCTCTGCATT | 319481 |
rs31306578 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr59 | Mm_Celera | 8:111487654 | CAGCAGAGGCTCTTC[A/G]GCTAGGACTCCCTGG | 319481 |
rs31306581 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Wdr59 | Mm_Celera | 8:111487881 | TCTATTTTGGTAAAA[A/T]GATACATCTCTTTAT | 319481 |
rs31306605 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Wdr59 | GRCm38.p3 | 8:111455229 | CCTCTCTACCTCACT[C/T]CTCTATCCCTAAGGC | 319481 |
rs31306608 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Wdr59 | GRCm38.p3 | 8:111455265 | CATTTCTACTATCAT[A/G]TCATAGGCATGCATG | 319481 |
rs31306611 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr59 | Mm_Celera | 8:111455364 | GAATTAGTTCACGTG[A/G]AAGGATAATCTCCAG | 319481 |
rs31306776 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Wdr59 | GRCm38.p3 | 8:111463277 | GAAAAAGCAATATAA[C/T]CATCGTACCCACTAC | 319481 |
rs31306779 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr59 | Mm_Celera | 8:111463341 | AGACACAAACTTTGA[A/G]TCAAGTCTATAATTT | 319481 |
rs31306782 | snp | C/G | 0.459184 | 0.136902 | intron-variant | Wdr59 | GRCm38.p3 | 8:111463362 | TCTATAATTTGAGAC[C/G]AGCAAGCAAATAAAA | 319481 |
rs31306804 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B, upstream-variant-2KB | Wdr59, Mir1957b | Mm_Celera | 8:111448463 | TGTGCACATCAGTCC[A/G]CCTGTTGTGGGACCA | 319481 |
rs31306807 | snp | C/T | 0.231111 | 0.249285 | downstream-variant-500B, upstream-variant-2KB | Wdr59, Mir1957b | Mm_Celera | 8:111448607 | GCACTGGTACCAAAC[C/T]TGGCACATAGTTCAA | 319481 |
rs31306810 | snp | G/T | 0.375 | 0.216506 | downstream-variant-500B, upstream-variant-2KB | Wdr59, Mir1957b | GRCm38.p3 | 8:111448615 | ACCAAACCTGGCACA[G/T]AGTTCAAGATCAAGC | 319481 |
rs31306813 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B, upstream-variant-2KB | Wdr59, Mir1957b | Mm_Celera | 8:111448619 | AACCTGGCACATAGT[C/T]CAAGATCAAGCTTAT | 319481 |
rs31306916 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr59 | Mm_Celera | 8:111467892 | CAGCCGTCAGTCTTT[C/T]TTGTCTTATTAGCTA | 319481 |
rs31306918 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr59 | Mm_Celera | 8:111467916 | TTAGCTAATGCTGAG[C/T]TCTGCTATCCAGTCT | 319481 |
rs31306921 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr59 | Mm_Celera | 8:111467977 | GATGCAGATGCACAG[A/G]CTTACTTAACACTGC | 319481 |
rs31306945 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Wdr59 | GRCm38.p3 | 8:111474515 | ATGAATGTGGGCATC[A/G]CTGGTGCCTGGCTCA | 319481 |
rs31306948 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Wdr59 | Mm_Celera | 8:111474830 | GGAACTAATTGATTT[A/C]ATATGAATGACTTGT | 319481 |
rs31306951 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Wdr59 | Mm_Celera | 8:111475139 | ACTTGCAATACTTGA[A/T]GGAAAAACTATCCCT | 319481 |
rs31307214 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr59 | Mm_Celera | 8:111487927 | CCTTTCAATTCTCTT[A/G]ATCAGCTGAATCGTG | 319481 |
rs31307216 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr59 | Mm_Celera | 8:111487994 | GTTTAGGGTGCTCCA[C/T]GAAACAGCTTATAAA | 319481 |
rs31307218 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr59 | Mm_Celera | 8:111488158 | ATGCTCTGTACTCAG[C/T]AACAGGGTAAGTGGG | 319481 |
rs31307221 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr59 | Mm_Celera | 8:111488278 | CACTATCTTGTCTCA[C/T]GTTCATGGGCATCAA | 319481 |
rs31307394 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr59 | Mm_Celera | 8:111456698 | CTGGGCTGAATCTAG[C/T]CCTGCTTCTTAGGTA | 319481 |
rs31307397 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr59 | Mm_Celera | 8:111457023 | TCATGGCCTGTTCTA[C/T]ACCCTGGCAGGGGCA | 319481 |
rs31307400 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr59 | Mm_Celera | 8:111457093 | TTTAAATTTCATCTC[C/T]GAGTCCCTCCTGGAG | 319481 |
rs31307403 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdr59 | GRCm38.p3 | 8:111457248 | CTTTGAATTTATTGC[C/T]AACCTTACTTTTCCC | 319481 |
rs31307576 | snp | C/T | 0.231111 | 0.249285 | downstream-variant-500B, upstream-variant-2KB | Wdr59, Mir1957b | Mm_Celera | 8:111448639 | ATCAAGCTTATGCCA[C/T]GGAGTCTCATGACCA | 319481 |
rs31307579 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | Wdr59, Mir1957b | Mm_Celera | 8:111448853 | GGGCTGGAGACAAAA[C/T]AGTTCTGACTTTGCA | 319481 |
rs31307582 | snp | C/T | 0.336735 | 0.234472 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | Wdr59, Mir1957b | GRCm38.p3 | 8:111448959 | CAAGGAACCAGATGG[C/T]CTCTTCTGTCCCACA | 319481 |
rs31307585 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Wdr59 | GRCm38.p3 | 8:111463430 | ACAAGGGCAACATAC[A/G]AAAAGTGACACACCA | 319481 |
rs31307588 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr59 | Mm_Celera | 8:111463445 | AAAAAGTGACACACC[A/G]GTATTGCTCCAAGTA | 319481 |
rs31307591 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr59 | Mm_Celera | 8:111463462 | TATTGCTCCAAGTAC[A/G]GACATGCAGCTCACA | 319481 |
rs31307614 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Wdr59 | Mm_Celera | 8:111475284 | AAATACTGATTGTCA[A/G]TGTTGAGGCCTGGTT | 319481 |
rs31307617 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Wdr59 | Mm_Celera | 8:111475784 | ATTCAACTAATGGGG[A/C]TTGCCAGGACAGATA | 319481 |
rs31307620 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Wdr59 | GRCm38.p3 | 8:111475909 | TCACAGCAATGACTG[C/T]TCCTACATAAACTAA | 319481 |
rs31307623 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Wdr59 | Mm_Celera | 8:111475945 | AAAGTGAAAGACCAG[A/G]GAGGGATTACTAACT | 319481 |
rs31307714 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr59 | Mm_Celera | 8:111467999 | TAACACTGCAACCTA[A/G]AACTGCAGTTTCTGT | 319481 |
rs31307717 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr59 | Mm_Celera | 8:111468077 | TGAGTTCTGTATAAT[C/T]ACTCTTTCAGGAATC | 319481 |
rs31307720 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr59 | Mm_Celera | 8:111468414 | CTTTTATCCAGTTGG[A/G]GCCGCTCACATAAGG | 319481 |