SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs752989845 | snp | A/G | 2.29495e-05 | 0.00338736 | intron-variant | CUL4B | GRCh38.p7 | X:120532611 | TGAAGAAGAAACAGA[A/G]GTTTAGTTATTTGTT | 8450 |
rs753016013 | snp | C/T | 2.7281e-05 | 0.00369321 | synonymous-codon, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560543 | CTTGGCAGAGGTGGG[C/T]GGAGTGGTGCTGGTA | 8450 |
rs753057150 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120551245 | GGAGTCTTGCTCTGT[C/T]GCCCAGATTGGGGTG | 8450 |
rs753062420 | snp | A/G | 0.000971867 | 0.0220225 | intron-variant | CUL4B | GRCh38.p7 | X:120539410 | TGTTTAATAACCGGG[A/G]AATACACGAGGTACT | 8450 |
rs753064141 | in-del | -/A | | | intron-variant | CUL4B | GRCh38.p7 | X:120530295 | AATTATACCAGAAGC[-/A]AAACCTGACTATTTA | 8450 |
rs753168322 | snp | C/G | 2.32393e-05 | 0.00340868 | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560356 | TCTTCTGTATCGGTA[C/G]GTGGCTGGAAGCAGC | 8450 |
rs753172656 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120572400 | AACCCAGGAGACGGA[G/T]GTTGCAGTGAGCCGA | 8450 |
rs753178107 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120551563 | ACCTTTAGGCAAGAT[C/T]TGGAGTGGTGTCTGT | 8450 |
rs753205902 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120535476 | TTAGGAGGCCGAGGC[A/G]CGTGGATCACAAGGT | 8450 |
rs753278971 | snp | C/G | | | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120576118 | GATTGCTCCTTTTTG[C/G]GTTCTTTGTCTTGAG | 8450 |
rs753289716 | snp | C/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | CUL4B | GRCh38.p7 | X:120559913 | CAAGGATCCTAACCA[C/G]CCCCGGAAAATGAAC | 8450 |
rs753356807 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120565757 | CTGAGACAGTGTCTC[A/G]CTCTGTCACCCAGGC | 8450 |
rs753379398 | snp | G/T | 3.29919e-05 | 0.00406138 | intron-variant | CUL4B | GRCh38.p7 | X:120540583 | ACAAAAAATTACCAC[G/T]TTTTACTGTAATCGA | 8450 |
rs753459012 | in-del | -/AG | | | intron-variant | CUL4B | GRCh38.p7 | X:120534802 | AGCTGACCTTTTAAC[-/AG]TTTTTTTTTAAGCCT | 8450 |
rs753469671 | snp | A/G | 0.000123246 | 0.00784907 | intron-variant | CUL4B | GRCh38.p7 | X:120539385 | TAGCTAAAATGGGGG[A/G]AAAGTTTGTTGTTTA | 8450 |
rs753488534 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120531647 | GTATTTTTAGTAGAG[A/G]CAGGGTATCGCCATG | 8450 |
rs753524758 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120533769 | CCCCTTTCCCTATGG[-/T]TTATATAAAGAGTTC | 8450 |
rs753541120 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120532750 | TAGCCAATGGCTTTT[C/T]TCCTAGTCCTCTTCT | 8450 |
rs753567527 | snp | C/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120563749 | ATGAACAAGGTTGTT[C/G]TAATTCATGTAGTTA | 8450 |
rs753629299 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120539959 | GAAGCACTGTAGTGT[A/G]TATCACATCCTTATG | 8450 |
rs753655895 | snp | A/C | 2.30521e-05 | 0.00339493 | intron-variant | CUL4B | GRCh38.p7 | X:120537043 | GCATATACTATAAGA[A/C]GATCAAAACACACAC | 8450 |
rs753692819 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120538996 | TCTTGATTGCATTAA[C/G]TTTTCTTCAGAAAAG | 8450 |
rs753737857 | snp | C/T | 0.00105904 | 0.0229869 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120525178 | GCAACTAGAAAGAAA[C/T]AGACGACTTTTTAAA | 8450 |
rs753795805 | snp | A/G | 0.00105904 | 0.0229869 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120562570 | TATATACAAAGTGCT[A/G]TCAGAAGAGGCAAAA | 8450 |
rs753812267 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120544356 | GATTGGGTTTTTATG[C/T]TCATATATGAGATGT | 8450 |
rs753818192 | snp | A/G | 2.32339e-05 | 0.00340829 | intron-variant | CUL4B | GRCh38.p7 | X:120536898 | ATGATTTCTATGCCT[A/G]TAACTCAGTTCTAAA | 8450 |
rs753832927 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120546647 | AGGATATTTTAAAGC[A/G]TTTGGTACAAGTCAT | 8450 |
rs753834632 | snp | C/G | 2.51515e-05 | 0.00354614 | intron-variant | CUL4B | GRCh38.p7 | X:120543847 | TATTGTTTTCCTCCC[C/G]ATAAATCATTCAGAA | 8450 |
rs753837282 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | CUL4B | GRCh38.p7 | X:120548914 | AGAACTGCATTTTTA[C/T]TTCACTTTAATAACT | 8450 |
rs753840169 | snp | C/T | 0.0145186 | 0.0839555 | missense | CUL4B | GRCh38.p7 | X:120535886 | ACTGCCACTGAAGTT[C/T]CCTGCCACTATGTTT | 8450 |
rs753851960 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120571318 | GGTTTTTTTAAAAAA[A/T]GTTTCAAGACAGGAA | 8450 |
rs753941445 | snp | C/G | 9.11587e-05 | 0.00675063 | missense | CUL4B | GRCh38.p7 | X:120574593 | CATCATTCCCATCTC[C/G]TGATCCAGATGACTG | 8450 |
rs753947452 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120557326 | AAGGGATTGCCCTTA[A/G]GAACTGCCCTTAAAA | 8450 |
rs754027121 | snp | C/T | 2.28029e-05 | 0.00337653 | intron-variant | CUL4B | GRCh38.p7 | X:120530089 | CTCAATAGGAAAACA[C/T]AGAAGTACCTACCTT | 8450 |
rs754033826 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120534116 | GGCTCATGCCTGTAA[C/T]TGCAGTACTTAGGGA | 8450 |
rs754043564 | snp | C/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560760 | AAGAGAGGAGAAACA[C/G]AGAGGACGAGAAGGA | 8450 |
rs754115143 | snp | A/G | 4.58295e-05 | 0.00478672 | synonymous-codon | CUL4B | GRCh38.p7 | X:120544487 | TTAACTTACTTGCAA[A/G]TCAGACAGCATGCTT | 8450 |
rs754155826 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120546471 | AGTTTTAAAAACTAA[C/T]ATTCCTGTATTTGAA | 8450 |
rs754181214 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120557196 | GATTACAGGTGTGAG[C/T]CACCGTGCCCGGCCT | 8450 |
rs754276183 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120536391 | GGATTCTCAATATCT[A/C]TCTGTCTAGCCTTAA | 8450 |
rs754299322 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120537816 | TTGCAAGCTCTGAAC[A/G]TGCAAATTACCAAAC | 8450 |
rs754317664 | snp | C/T | 2.31086e-05 | 0.00339908 | synonymous-codon, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560339 | GTCTTCAAAACGCAG[C/T]TTCTTCTGTATCGGT | 8450 |
rs754321676 | snp | A/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120572242 | GCCAAGGCAGGTGGG[A/T]CACTTGAAGTCAGGA | 8450 |
rs754330779 | in-del | -/GAG | | | cds-indel, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560261 | GCAGTTGGTGAAGAT[-/GAG]GAGGAGGAGGAGGAG | 8450 |
rs754353328 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120527672 | TACATAGCCTGAAGA[C/T]AATTTTATACCTTTT | 8450 |
rs754427789 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120563300 | CTGCAGTGGTGTAAT[C/T]TTGGCTCACTGCAAC | 8450 |
rs754478964 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120566698 | CACCGCACCCAGCCA[A/T]ATTTCATATTTTTAG | 8450 |
rs754480407 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | CUL4B | GRCh38.p7 | X:120531600 | AAGTAGCTGGGACTA[C/T]AAGCACGCACCACCA | 8450 |
rs754482838 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120529380 | CTATTATTATCTCAG[C/T]TTTACAAAAGAGGAA | 8450 |
rs754500087 | in-del | -/T | 2.32339e-05 | 0.00340829 | intron-variant | CUL4B | GRCh38.p7 | X:120536898 | TGATTTCTATGCCTA[-/T]TAACTCAGTTCTAAA | 8450 |
rs754503890 | in-del | -/TG | 0.00475684 | 0.0485365 | intron-variant | CUL4B | GRCh38.p7 | X:120566367 | ATATATATATATATA[-/TG]TATATATATATATAT | 8450 |
rs754507926 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120531878 | AAGACAGGCTCTCAT[A/C]TGCTGCTGGACAGAG | 8450 |
rs754548912 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120551104 | AAACTTAAATACTTG[C/T]CTTCCCCAATAAAAG | 8450 |
rs754556559 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120574718 | GACTCTGGTTTCCCA[A/G]CCAATTTTATCCTAT | 8450 |
rs754700093 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120571403 | AGATAACAAATGACA[A/C]CTAGGATTGATTTTT | 8450 |
rs754725082 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120563816 | TAAAAAATTACAAAT[A/G]TTAGTGCAACTGAAA | 8450 |
rs754817069 | snp | A/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120565215 | GGTCCTCTCCAGATA[A/T]CTCATACCAGTGGCT | 8450 |
rs754840865 | snp | A/G | 2.72127e-05 | 0.00368858 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560648 | AAACATGAAAATAGC[A/G]GGGTCAACAGGCAGA | 8450 |
rs754862364 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120570636 | AGGATTTTCTATTCC[C/T]ATTCTGCATGCAGAC | 8450 |
rs754893377 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120557286 | TGTGTGTCAAATACA[C/T]AGTAGGGAAAAATTT | 8450 |
rs755039915 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120545525 | ATCATGATCTGCCAA[C/T]GAAAAAAAAAGAAAT | 8450 |
rs755058372 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120555158 | TACAAGAAAACAAAA[A/G]CAAGAGATGCAAGCT | 8450 |
rs755058490 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120544309 | GTTTTTAAACATCAA[G/T]CTAGGATCCTTTTGT | 8450 |
rs755090198 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120557416 | GCTGGACTACAAACT[A/G]CTACTCATTTCTGGG | 8450 |
rs755105687 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120559071 | TTGAGACAAAATAGA[A/G]CATACTCCTGATTTC | 8450 |
rs755137297 | snp | C/T | | | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120525202 | TTTTAAAATACCTGG[C/T]CACAGGTCTTTGAGA | 8450 |
rs755140459 | snp | A/G | 2.27944e-05 | 0.00337589 | synonymous-codon | CUL4B | GRCh38.p7 | X:120530119 | TTACTGGAAATTTCA[A/G]CTGGTTGTACACTTC | 8450 |
rs755174339 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120565338 | AGATGTTTCTGAGAA[C/T]GCATTAAAAAAACAC | 8450 |
rs755187457 | snp | C/T | | | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561257 | TAGTTCGCTCCTGCT[C/T]CCGCTCCCCTTCGCG | 8450 |
rs755264973 | snp | C/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120536545 | TAGGTAGAGTGAGGG[C/G]TATAACCTGGGAAGA | 8450 |
rs755298336 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120529853 | AAACTTGAAAATTTC[A/T]AACACTCATTTAGCA | 8450 |
rs755306871 | snp | A/C | 2.31313e-05 | 0.00340075 | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560345 | AAAACGCAGCTTCTT[A/C]TGTATCGGTACGTGG | 8450 |
rs755322216 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120525738 | CAAAGAGAAGAGTTG[A/G]GATGCTTCTAAAAAA | 8450 |
rs755326544 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120570597 | AGACATGGCACAAAG[A/G]AGAAAGTGATTTAGA | 8450 |
rs755331312 | snp | A/G | 4.68494e-05 | 0.00483968 | intron-variant | CUL4B | GRCh38.p7 | X:120538775 | AACATCCTTGCCTAT[A/G]TAAAAAGAAATGCAA | 8450 |
rs755414461 | in-del | -/ACAC | | | intron-variant | CUL4B | GRCh38.p7 | X:120543500 | TTACCTTCTAAACAC[-/ACAC]ACACACACACACACA | 8450 |
rs755438047 | in-del | -/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120548249 | ACTGCACTCTAGCCT[-/G]GGGACAAAGTGAGAC | 8450 |
rs755459703 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561291 | CCCTTTCCTGGCAGC[A/G]CCTTCCTTCCCTGGC | 8450 |
rs755479779 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120534858 | ATTAATCAGCCTTAT[G/T]TGTCATTCTAGATAT | 8450 |
rs755523179 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120528873 | TATCTTCATGATTGC[A/G]TTCTAAGCTCCTGGA | 8450 |
rs755530618 | snp | G/T | 4.34056e-05 | 0.00465842 | intron-variant | CUL4B | GRCh38.p7 | X:120539393 | ATGGGGGAAAAGTTT[G/T]TTGTTTAATAACCGG | 8450 |
rs755557315 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120572396 | CTTGAACCCAGGAGA[A/C]GGAGGTTGCAGTGAG | 8450 |
rs755573305 | in-del | -/CA | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120568670 | ATTTGTAGTTGATTT[-/CA]CAGTTTTTCAAAGCA | 8450 |
rs755600927 | snp | A/T | 2.28796e-05 | 0.0033822 | missense | CUL4B | GRCh38.p7 | X:120532591 | CTCCTTAACTCTCCA[A/T]CCTCTGAAGAAGAAA | 8450 |
rs755615960 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120549827 | TTTAGTATTCCTCTC[A/C]TTGTATCTCACCGTT | 8450 |
rs755627583 | snp | A/G | 4.9694e-05 | 0.00498443 | intron-variant | CUL4B | GRCh38.p7 | X:120539382 | ACTTAGCTAAAATGG[A/G]GGAAAAGTTTGTTGT | 8450 |
rs755630142 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120527438 | TTTTTAATAGACAGG[G/T]TCTTGCTATGTCGCC | 8450 |
rs755632335 | snp | C/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120551364 | CGCCACACTCAGCTA[C/G]GTTTTTTTGCATTTT | 8450 |
rs755643323 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120557564 | TTGAGGCCTTTCCTA[C/T]GGGTAGGTAACACAA | 8450 |
rs755685217 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120567539 | GTCAGTCCAATTCAA[G/T]CAGAATCTCTGTGAG | 8450 |
rs755717522 | snp | C/T | 4.58169e-05 | 0.00478606 | synonymous-codon | CUL4B | GRCh38.p7 | X:120538739 | GCGCTTGGCTAAATC[C/T]TTCTTATAGAAGGCC | 8450 |
rs755721842 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120528992 | AAATGACCACTTGTT[A/C]AAGAGGGGAAAAGAG | 8450 |
rs755742485 | snp | C/G | 4.57017e-05 | 0.00478004 | intron-variant | CUL4B | GRCh38.p7 | X:120574666 | TTCACTTTTCCAGCA[C/G]TCCTCTCCCATATCT | 8450 |
rs755798890 | snp | A/T | 2.87125e-05 | 0.00378886 | intron-variant | CUL4B | GRCh38.p7 | X:120546504 | AATGTTTTTAACTAT[A/T]AATACAATGTTTAGC | 8450 |
rs755828838 | snp | C/T | 0.00791544 | 0.0624105 | intron-variant | CUL4B | GRCh38.p7 | X:120531749 | ACAGGTGTGAACCAC[C/T]GTACCTGGCCCACCT | 8450 |
rs755854013 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120538880 | AGTTATTTTACTTTA[C/T]ACATTTTATTTAAGT | 8450 |
rs755867136 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120542802 | TTCAGATAAGAAAAC[C/T]GGCACCTCCAGGAAG | 8450 |
rs755868778 | snp | A/C | 2.28378e-05 | 0.00337911 | intron-variant | CUL4B | GRCh38.p7 | X:120530274 | CAAAAAAGTTTTAAA[A/C]CTAGGAATTATACCA | 8450 |
rs755915780 | in-del | -/A | 0.497499 | 0.0352757 | intron-variant | CUL4B | GRCh38.p7 | X:120572465 | AGAGCAAAACTCCTC[-/A]AAAAAAAAAAAAAAA | 8450 |
rs755941543 | snp | A/G | 0.0001646 | 0.00907044 | intron-variant | CUL4B | GRCh38.p7 | X:120539419 | ACCGGGGAATACACG[A/G]GGTACTGGGCACTAT | 8450 |
rs755952239 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120538033 | AATTACAACAAACAC[A/G]TTTCTATTTATCCTC | 8450 |
rs755955291 | snp | C/T | | | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120562555 | AACAATAATATGACA[C/T]ATATACAAAGTGCTG | 8450 |
rs755958060 | snp | C/T | 2.31163e-05 | 0.00339965 | missense | CUL4B | GRCh38.p7 | X:120544618 | CACTTATAATATGAG[C/T]CCTAAATAACTCCAG | 8450 |
rs755967424 | snp | C/G | 0.00211696 | 0.0324653 | intron-variant | CUL4B | GRCh38.p7 | X:120528616 | GTCCCAGCTACTCGA[C/G]AGGCTGAGGCAAAAG | 8450 |
rs755973631 | snp | A/G | | | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120563514 | AGTGCTGGGCCTACC[A/G]TATAGTTCTTGCTGC | 8450 |
rs756041930 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120548285 | CTCAAAAATAAAAAA[C/G]CTGTCTTGTTTAAAA | 8450 |
rs756058777 | in-del | -/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120569361 | ACCTTAGGGAAGTTT[-/C]TTTTTTTTTTTTTTT | 8450 |
rs756118747 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120570348 | GTTTGGAAACCACAG[C/T]CCATGGACCAAACCC | 8450 |
rs756152694 | snp | A/G | 2.50222e-05 | 0.00353702 | synonymous-codon | CUL4B | GRCh38.p7 | X:120543015 | AAGTTGTTTTTCTAC[A/G]GTAGCAATTAATGAC | 8450 |
rs756182291 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120535477 | TAGGAGGCCGAGGCG[C/T]GTGGATCACAAGGTC | 8450 |
rs756183673 | snp | C/T | 0.000173756 | 0.00931922 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561323 | CACCGGGAACTCCCA[C/T]TCCCTCCTTAACGGT | 8450 |
rs756198708 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120534880 | TCTAGATATTCATCA[C/T]AAGCAGCAAGAAATC | 8450 |
rs756228337 | in-del | -/A | 0.00211752 | 0.0324696 | intron-variant | CUL4B | GRCh38.p7 | X:120546408 | AATTTTTAAAAAAAG[-/A]AAAAAAAAAGAAAAG | 8450 |
rs756240885 | snp | C/T | 3.29207e-05 | 0.004057 | upstream-variant-2KB, missense, intron-variant | CUL4B | GRCh38.p7 | X:120561395 | ACTGGGCAGACACTT[C/T]TCATAGCGCCCAGAT | 8450 |
rs756244778 | snp | C/T | | | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120577232 | TGGACATCTATGCTT[C/T]ATTCCTGAATTTCAG | 8450 |
rs756247517 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120545612 | TGAAGAGTTTGTCTG[C/T]ATATATATTACATTA | 8450 |
rs756273328 | snp | A/G | 0.0152462 | 0.0859689 | intron-variant | CUL4B | GRCh38.p7 | X:120569506 | GCTGGGACTACAGGC[A/G]CCCGCCACCACGCCC | 8450 |
rs756316494 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120556407 | AAAAAAGTTTGACTC[A/G]TGATACCATCTTATA | 8450 |
rs756319401 | snp | A/G | | | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120524841 | AGAATTAAGAGCCTC[A/G]GGGAGGGGACCCGCT | 8450 |
rs756404358 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120555318 | TACAAATATGGAATA[C/T]ATAAAATATTATTGA | 8450 |
rs756411375 | in-del | -/GAGGAGGAG | 4.677e-05 | 0.00483558 | cds-indel, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560262 | GCAGTTGGTGAAGAT[-/GAGGAGGAG]GAGGAGGAGGATTCC | 8450 |
rs756499309 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120527635 | TCTAAACACAAAATT[C/T]ATCTATGTTTCATAC | 8450 |
rs756530686 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120541928 | TATAGAGACTTTAGT[C/T]GCTATAAAAATAAAA | 8450 |
rs756533533 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120562446 | TGATCATTCTAACTG[C/T]AAAAGCATTCAGTTA | 8450 |
rs756548714 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120551254 | CTCTGTCGCCCAGAT[C/T]GGGGTGCAATCTTGG | 8450 |
rs756644217 | in-del | -/TG | | | intron-variant | CUL4B | GRCh38.p7 | X:120550716 | TCGGAGGGAACATTC[-/TG]TTTTTCTAATTTAGC | 8450 |
rs756655536 | snp | A/G | 2.31924e-05 | 0.00340524 | intron-variant | CUL4B | GRCh38.p7 | X:120538073 | AATCATAGCAAGCAG[A/G]TAACTAAATACAACT | 8450 |
rs756661336 | in-del | -/TAAAGA | 2.2805e-05 | 0.00337668 | intron-variant | CUL4B | GRCh38.p7 | X:120535785 | GGATGACCTAAACAT[-/TAAAGA]TAAAGATGAAAACTA | 8450 |
rs756662557 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120526916 | GCTCAAGCCCATTTA[A/G]TTAATACCCCATTAA | 8450 |
rs756665325 | snp | A/G | 2.2924e-05 | 0.00338548 | synonymous-codon | CUL4B | GRCh38.p7 | X:120538136 | TACCTGTTTGAACTG[A/G]ATCATGATGTCTTTA | 8450 |
rs756722808 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120547598 | ATTTTGGGGGGCCAA[G/T]GTGAGAGGATTGCTT | 8450 |
rs756739337 | snp | G/T | 2.70168e-05 | 0.00367528 | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558031 | AGTTTTCTGGTAATT[G/T]AGGCTTATCTAGATG | 8450 |
rs756743891 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120570169 | TGAGCCACACTGGTT[C/T]AGGAATTGGATTTAC | 8450 |
rs756751250 | snp | A/G | 5.87441e-05 | 0.00541928 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558058 | GATGATATGTAAAAG[A/G]TTGGCATCAGAATAC | 8450 |
rs756814955 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120568287 | TATTGCCTAGGGCCA[A/G]TCCTGCTTTTTGATG | 8450 |
rs756850520 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120549349 | ATGAGGTCTGGAGTT[C/T]GAGACCACTCTGACC | 8450 |
rs756856664 | snp | A/C | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558909 | ATCCATATATTTTTA[A/C]GTGAAATAATGAAAA | 8450 |
rs756920132 | snp | A/G | 2.28943e-05 | 0.00338329 | intron-variant | CUL4B | GRCh38.p7 | X:120538644 | AGAAAAGGAACAGAA[A/G]GAATGAGAAACCTAC | 8450 |
rs756933424 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120530924 | TGGTACAGCATAAAT[A/G]TTTTAAAAGTAAGGA | 8450 |
rs756976588 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120555445 | TTATAAAGAGCTTTT[C/T]CCCTAAAGTAAAACA | 8450 |
rs757023560 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120540147 | TAAAGGTAAATAGTG[C/T]CCAACGTACTGTCTT | 8450 |
rs757062628 | in-del | -/TTTT | | | intron-variant | CUL4B | GRCh38.p7 | X:120534804 | CTGACCTTTTAACAG[-/TTTT]TTTTTAAGCCTTATA | 8450 |
rs757084217 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120559604 | TGAGTTTCATGAATA[C/T]AGTATAAATCTAATT | 8450 |
rs757084583 | snp | A/G | 4.56059e-05 | 0.00477502 | intron-variant | CUL4B | GRCh38.p7 | X:120574519 | CAATTATTTAGACTT[A/G]ACTCTTGAGTTTTAC | 8450 |
rs757094409 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120529923 | CCTTTTGTCACTGCT[A/G]CCCACATATGCCAAC | 8450 |
rs757097002 | snp | C/T | | | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120562112 | CCAGGATCGTCCTAA[C/T]CCCCACTCTATCAGT | 8450 |
rs757189952 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120565541 | ACAAAAATTAGCCAG[G/T]CCTGGTGGTGCACAT | 8450 |
rs757200154 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120564577 | TGCCACTACACTCCT[A/G]CCTGGGCAACAGAGA | 8450 |
rs757205619 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120574634 | CGTCCTTTGGGTCTA[C/T]GATAGAAAACAGAGA | 8450 |
rs757235110 | snp | C/T | 1.64746e-05 | 0.00287002 | missense | CUL4B | GRCh38.p7 | X:120544605 | TGCACTTTCTGATCA[C/T]TTATAATATGAGCCC | 8450 |
rs757298030 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120538932 | AGAGATCCATTTTTG[C/T]GCCAGACATTTCGAA | 8450 |
rs757326564 | snp | C/T | 2.80143e-05 | 0.00374251 | intron-variant | CUL4B | GRCh38.p7 | X:120544083 | TATTGTGAGAGACAG[C/T]GAGAATTTATTAGTC | 8450 |
rs757340525 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120541271 | TTGGGAGGCCAAGGC[A/G]GGTGGATCATTTGAG | 8450 |
rs757374498 | snp | G/T | 0.000596105 | 0.0172539 | intron-variant | CUL4B | GRCh38.p7 | X:120536921 | GTTCTAAACAGTAAC[G/T]CTTACCTCTGGTGGT | 8450 |
rs757398611 | snp | C/G | 6.67156e-05 | 0.00577524 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561359 | GGGAAGCTTCGCGCC[C/G]CAGCGCCCTTACCGG | 8450 |
rs757427816 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120562574 | TACAAAGTGCTGTCA[A/G]AAGAGGCAAAACAAG | 8450 |
rs757437276 | in-del | -/CTGA | 4.57519e-05 | 0.00478266 | intron-variant | CUL4B | GRCh38.p7 | X:120530300 | TACCAGAAGCAAAAC[-/CTGA]CTATTTACATAAATT | 8450 |
rs757448605 | snp | A/G | 9.12253e-05 | 0.0067531 | intron-variant | CUL4B | GRCh38.p7 | X:120541560 | ACTCTTGATGTGTAG[A/G]TAAGCCATAAGAGAG | 8450 |
rs757457910 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120535691 | ACTCTGGTGACAGAG[G/T]GAGACTCTGTCTCAA | 8450 |
rs757541076 | snp | A/T | 2.73422e-05 | 0.00369734 | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560576 | ACCATCAGTGGCAGA[A/T]CTGACCTCCTGAGCA | 8450 |
rs757605130 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120574742 | ATCCTATTTGTTCCA[C/T]ATCTTCAAGGAAATT | 8450 |
rs757614423 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120567700 | CCTGGTCAACAAAGC[A/G]AGACCCTGTCTCTAT | 8450 |
rs757649304 | snp | C/T | 5.05299e-05 | 0.00502617 | missense | CUL4B | GRCh38.p7 | X:120542981 | CTTTCTGAAGAATTG[C/T]TGTTAAGTGTTCACC | 8450 |
rs757688679 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120532842 | GCTCAAGTGATCCAC[C/T]CGCCTTGGCCTCCCA | 8450 |
rs757689109 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120543873 | CAGAAAATGTCAAGT[A/C]CAAAAGATCCTGGAA | 8450 |
rs757709300 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120543108 | CTCTCCTGAGGGGGG[-/A]AAAAAAATCAAATAG | 8450 |
rs757744958 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120531978 | CCTTTAACCCAAAAA[A/G]ATCTACTTCCACAAA | 8450 |
rs757749038 | snp | C/T | 2.33138e-05 | 0.00341414 | missense | CUL4B | GRCh38.p7 | X:120547164 | GAATCTGTGCTTTGA[C/T]GTGATCTTCGCAGAT | 8450 |
rs757756585 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120528439 | TCACTATTTAAAAGA[A/C]TACTGGACAGGTGCA | 8450 |
rs757826357 | snp | A/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120533777 | CCCTATGGTTATATA[A/T]AGAGTTCTGGCCAGG | 8450 |
rs757852741 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120566973 | ATATATATATTTGGC[A/G]AGCTGATGTGCCATG | 8450 |
rs757892590 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120540254 | TGATATACCAGCTAA[A/G]CAACCTCAAACAAAT | 8450 |
rs757896094 | snp | C/T | 0.000113947 | 0.00754722 | missense | CUL4B | GRCh38.p7 | X:120574598 | TTCCCATCTCCTGAT[C/T]CAGATGACTGTGACA | 8450 |
rs757904039 | in-del | -/CTTTTCTTTTTT | 0.00211696 | 0.0324653 | intron-variant | CUL4B | GRCh38.p7 | X:120573818 | TGAGGAATTTCCTTC[-/CTTTTCTTTTTT]CTTTTCTTTTTTTTG | 8450 |
rs757938851 | snp | A/G | 0.00105904 | 0.0229869 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561113 | CGGTCACGCGGCGCC[A/G]AGGGAGGGGCGGTGT | 8450 |
rs757938923 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120545110 | CTATTCTATTTTCGT[A/G]TATACATGGACTTTT | 8450 |
rs757952500 | in-del | -/T | 0.479467 | 0.0992222 | intron-variant | CUL4B | GRCh38.p7 | X:120565723 | GGGCAGTCCATTTAC[-/T]TTTTTTTTTTTTTTT | 8450 |
rs758021572 | snp | C/T | 2.30585e-05 | 0.00339539 | intron-variant | CUL4B | GRCh38.p7 | X:120535982 | TATTTAAGCTCTGTA[C/T]CCAATACCACATTTA | 8450 |
rs758043399 | snp | C/T | 3.29516e-05 | 0.00405891 | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558009 | TTTTGCCAGGTTTCA[C/T]CTGTGTAGTTTTCTG | 8450 |
rs758045664 | in-del | -/AGG | 2.32599e-05 | 0.00341019 | cds-indel, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560432 | ATCCCTGGGTTGTAA[-/AGG]AGGAGTGGAAGAGGA | 8450 |
rs758177212 | snp | A/G | 0.00105904 | 0.0229869 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120525457 | AAAATCAGTGACAGT[A/G]AAGAGAAGCCTTTGC | 8450 |
rs758271456 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120556557 | TTAAATTGAGAGTGA[C/T]GGCTGGGTTTGGTAG | 8450 |
rs758299358 | in-del | -/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120536462 | AGGAGTCAGGATAGA[-/T]TTAATCAAGGACCCA | 8450 |
rs758361600 | snp | A/G | 0.0946423 | 0.195867 | intron-variant | CUL4B | GRCh38.p7 | X:120566361 | TATATATATATATAT[A/G]TATATATATATATAT | 8450 |
rs758374917 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120530943 | TAAAAGTAAGGACAT[A/G]GTAATCCTTTAAGAA | 8450 |
rs758451325 | in-del | -/C | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120553918 | AAAACAAGACACATT[-/C]TTTTTAAGCGTAGAG | 8450 |
rs758469566 | snp | A/C | | | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120559369 | ACTCTCCTCACATAT[A/C]TCAAACACGGTCTGA | 8450 |
rs758480204 | snp | A/T | 3.39628e-05 | 0.00412071 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CUL4B | GRCh38.p7 | X:120561415 | AGCGCCCAGATCCCG[A/T]AGCCCCCAGGTCCGC | 8450 |
rs758487912 | snp | A/G | | | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561718 | AATAGAAACTTTGAA[A/G]GAGATGAAAGAATAA | 8450 |
rs758490069 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120536675 | CAGTTGGTATTTGGT[G/T]TTGGTGCGCTTACTG | 8450 |
rs758494473 | snp | A/G | 2.3002e-05 | 0.00339123 | intron-variant | CUL4B | GRCh38.p7 | X:120532627 | GTTTAGTTATTTGTT[A/G]CCAGCATGAACAACT | 8450 |
rs758539355 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120564381 | GAGGCTGAGGCGGGC[C/T]GATCACCTGAGGTCA | 8450 |
rs758541097 | in-del | -/A | 0.00896606 | 0.0663524 | intron-variant | CUL4B | GRCh38.p7 | X:120552671 | AAAAAAAAGTGTCTG[-/A]AAAAAAAACACAGTC | 8450 |
rs758581715 | snp | C/T | 2.28071e-05 | 0.00337684 | synonymous-codon | CUL4B | GRCh38.p7 | X:120530246 | TGTAGTGCTTGCTTG[C/T]TCTTCAACCTAACAA | 8450 |
rs758583238 | snp | C/G | 4.65463e-05 | 0.004824 | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560364 | ATCGGTACGTGGCTG[C/G]AAGCAGCCACTGAAA | 8450 |
rs758590945 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | CUL4B | GRCh38.p7 | X:120527742 | GGTAAAGTGTGGAAT[C/T]TTCCACCTGTGGCAT | 8450 |
rs758718895 | snp | C/T | 2.98094e-05 | 0.00386054 | intron-variant | CUL4B | GRCh38.p7 | X:120540600 | TTTACTGTAATCGAA[C/T]TGTCTACAATGAAAA | 8450 |
rs758737173 | in-del | -/T | 0.00687095 | 0.0582088 | intron-variant | CUL4B | GRCh38.p7 | X:120537979 | CTTATATTTCACCAA[-/T]TTTTTTTTTCTACTG | 8450 |
rs758768060 | snp | A/G | 2.27902e-05 | 0.00337559 | synonymous-codon, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560129 | AGAGCCAGGTTTGCT[A/G]TTAGCAAAGCTAGAG | 8450 |
rs758781480 | snp | C/G | 0.000109969 | 0.00741433 | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560553 | GTGGGCGGAGTGGTG[C/G]TGGTATTACCATCAG | 8450 |
rs758790484 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120534718 | ATCCAGCAAAGCCAC[C/T]TGACGTGGTAATACA | 8450 |
rs758791298 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120544061 | TTATATTCTACAAAG[G/T]AAGGTCTATTGTGAG | 8450 |
rs758822613 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120572542 | AAAATAAGGTGAAAT[A/C]TCCACTCAGTCCCTG | 8450 |
rs758891153 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120551570 | GGCAAGATTTGGAGT[G/T]GTGTCTGTAAAACAG | 8450 |
rs758939648 | snp | C/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120554537 | CTTTAAAAAGACAAT[C/G]TTTGCTTACTGCAAG | 8450 |
rs759011320 | snp | A/T | 2.77439e-05 | 0.0037244 | intron-variant | CUL4B | GRCh38.p7 | X:120540585 | AAAAAATTACCACTT[A/T]TTACTGTAATCGAAT | 8450 |
rs759026954 | snp | A/G | 2.76671e-05 | 0.00371925 | intron-variant | CUL4B | GRCh38.p7 | X:120542939 | ACCATTTAAAAAGCA[A/G]TCTCTTATTTACAAA | 8450 |
rs759084602 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120542742 | ATATCAACCACTGTT[C/T]TTTTATTGGTATTTG | 8450 |
rs759113058 | snp | C/G | 6.92917e-05 | 0.00588566 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561329 | GAACTCCCACTCCCT[C/G]CTTAACGGTCCCGCG | 8450 |
rs759134187 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120535220 | CAAATAAATAAAAAT[A/C]GGAAGTGGCAGTGTA | 8450 |
rs759134495 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120563898 | CTTTTCTACTAACCT[A/G]AATGATAGCTGAGTC | 8450 |
rs759147637 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120556657 | CCAGCCTGGGCAACA[C/T]AGCAAGACCCCTATC | 8450 |
rs759162032 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120533337 | AAGTGGTCCAAATAA[G/T]TACTTCCACCATGCC | 8450 |
rs759195145 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120528222 | GACCAGACTGGCTAA[A/C]ATGGCAAAACCCCAT | 8450 |
rs759251227 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558423 | CTATGTGCAAGGTAC[C/T]TTATAAGCCTCTTAA | 8450 |
rs759263269 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120569048 | CATGCAGTTCAGGCC[A/G]CCATCAAGCAGGTAG | 8450 |
rs759338981 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120567335 | TTTTGCCATGTTGGC[C/T]AGGCTGGTCTTGAAC | 8450 |
rs759355752 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120533456 | TAACTCACTATTCTA[C/T]GTTACAATTAAGCTC | 8450 |
rs759468425 | snp | A/G | 0.000176351 | 0.00938853 | intron-variant, missense | CUL4B | GRCh38.p7 | X:120559796 | GCAAAATCCGGATCA[A/G]TCATACCGATTGTCA | 8450 |
rs759472167 | in-del | -/ATTT | 2.74033e-05 | 0.00370147 | intron-variant | CUL4B | GRCh38.p7 | X:120544232 | AAAATGAAGGAGATC[-/ATTT]ATTTAGCAAATATTT | 8450 |
rs759479405 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120571459 | TTTCTGGAAATTACT[C/T]AAGGGCGGGGGATGC | 8450 |
rs759521221 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120532351 | TTACAGGTATAAAAA[C/T]CTTTATATATTTTGA | 8450 |
rs759535317 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120565971 | CTGACCTCATGATCC[A/G]CCCGCCTCGGCCTCC | 8450 |
rs759612072 | in-del | -/TT | | | intron-variant | CUL4B | GRCh38.p7 | X:120567119 | CAAGGCCAATTTAGA[-/TT]TTTTTTTTTTTTTTT | 8450 |
rs759619904 | snp | A/G | 2.29261e-05 | 0.00338563 | synonymous-codon | CUL4B | GRCh38.p7 | X:120544526 | TCGAAGTAAACTTCT[A/G]TCAATTGCTTCACCA | 8450 |
rs759645444 | in-del | -/G | | | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120557630 | CCAGAAATCATCTTT[-/G]GGATTCATGCTATAG | 8450 |
rs759651045 | snp | A/G | 0.110699 | 0.207594 | intron-variant | CUL4B | GRCh38.p7 | X:120566391 | TATATATATATATAT[A/G]TATATATATTTGGGT | 8450 |
rs759759999 | snp | A/G | | | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120525730 | TTTATCAACAAAGAG[A/G]AGAGTTGGGATGCTT | 8450 |
rs759765793 | snp | A/T | 2.33081e-05 | 0.00341372 | intron-variant | CUL4B | GRCh38.p7 | X:120534624 | TAGTCATCACTTTTT[A/T]AAAAACACATGAAAA | 8450 |
rs759774336 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120528090 | TTCATTTTTATAAAT[C/T]AAGATTTAAAACGTA | 8450 |
rs759780489 | in-del | -/GGCTA | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120574371 | CCCACAACCACGCCC[-/GGCTA]GGCTAATTTTTTGTA | 8450 |
rs759794248 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120571162 | GTAATGTTCTAGTTC[-/T]TACACACAGATGATA | 8450 |
rs759828693 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120536660 | AGTAAAACATTAAAG[A/C]AGTTGGTATTTGGTG | 8450 |
rs759848627 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120539831 | TTGCTACATGTTTAC[G/T]GATACATAGTAGATA | 8450 |
rs759897080 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120540677 | TAAAAAGTAAGATAA[A/G]GCTATTTTTAAGATG | 8450 |
rs759913859 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120546781 | TTTGTAAAAGAAAAA[A/C]AAAACATAGTTTATA | 8450 |
rs759916112 | snp | A/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560731 | AGCAATGCTAGAGGG[A/G]GAAGGGAAGAAAGAA | 8450 |
rs759951965 | snp | A/G | 2.47893e-05 | 0.00352052 | synonymous-codon, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560501 | ACTGTTACTGCTGCT[A/G]CTGCTGCTGCTGTTT | 8450 |
rs759953816 | in-del | -/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120562120 | TCCTAACCCCCACTC[-/T]TATCAGTCCTTAACT | 8450 |
rs759981765 | snp | C/T | 6.85855e-05 | 0.0058556 | synonymous-codon | CUL4B | GRCh38.p7 | X:120532584 | CAGTGTTCTCCTTAA[C/T]TCTCCATCCTCTGAA | 8450 |
rs760159079 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120568202 | AGCCACTGCAATAGG[C/G]AGTGGTGAGAGGTGA | 8450 |
rs760186309 | in-del | -/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120532746 | GTTCTAGCCAATGGC[-/T]TTTTTCCTAGTCCTC | 8450 |
rs760207253 | snp | G/T | 2.34151e-05 | 0.00342155 | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560469 | GAGGTGGAATCAAAG[G/T]CTTCTCTCTCGTTAC | 8450 |
rs760245354 | snp | A/G | | | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120575929 | CTCCACGTGGTCTCT[A/G]CTGAGCGGGAAAAGG | 8450 |
rs760279493 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120554191 | CAGGAACTGTGATAA[C/T]TACTTTTTTGCAATA | 8450 |
rs760282749 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120554460 | GCCTCACACCCACAG[G/T]ATCTCAAGGTTGTCA | 8450 |
rs760294805 | snp | C/G | 9.19646e-05 | 0.0067804 | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560320 | ACCCTACAAACTCCA[C/G]GGTGTCTTCAAAACG | 8450 |
rs760403327 | snp | C/T | 1.64795e-05 | 0.00287045 | missense | CUL4B | GRCh38.p7 | X:120540547 | CAGGATTAATTACAA[C/T]AGTGCTGCCAAATGC | 8450 |
rs760443059 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120556427 | ACCATCTTATATTTG[C/T]AAGATTATAGTGCCT | 8450 |
rs760479973 | snp | A/T | 0.000529661 | 0.016265 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560954 | CTGCAGGAGCGACTC[A/T]GCGAGTCTGTGAGGC | 8450 |
rs760509559 | in-del | -/TATA | | | intron-variant | CUL4B | GRCh38.p7 | X:120556904 | TATTGTACTCTGAAG[-/TATA]TATATATTTTTTTTT | 8450 |
rs760511816 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120573336 | TTACAGTAAAAATAT[A/G]CCATATTGTATTAAA | 8450 |
rs760533226 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120533134 | AAACCCTAAAATCAT[C/T]TTTTAACTTTTCCTT | 8450 |
rs760569808 | snp | C/G | 0.000529661 | 0.016265 | intron-variant, utr-variant-5-prime | CUL4B | GRCh38.p7 | X:120559883 | GCACAGAAACACCCG[C/G]TGTATGCTTCAGCAC | 8450 |
rs760569882 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120568964 | CCAAGAGAAAAAAAT[A/G]AAGAATAAGAAAATA | 8450 |
rs760599297 | snp | C/T | 6.88192e-05 | 0.00586557 | intron-variant | CUL4B | GRCh38.p7 | X:120541750 | ATTTTGGCATTAAAA[C/T]ATAGTGAACAAAAAA | 8450 |
rs760606419 | snp | C/G | 1.75634e-05 | 0.00296334 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CUL4B | GRCh38.p7 | X:120561445 | CAGGACTTGAGTGGG[C/G]GGGGGAAGGGGGGAG | 8450 |
rs760665616 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120546912 | GATAGGGCAAAAAGG[A/G]TAAAGACATAAGGAC | 8450 |
rs760685836 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120557067 | CAGGCATGCACCACA[C/T]TGCCTGGCTAATTTT | 8450 |
rs760723480 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120546541 | ACAATACTTTTTCCA[G/T]CTTACCATTTGTCTG | 8450 |
rs760806030 | snp | C/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120568767 | CTGTACAGATAAGAA[C/G]TAGGCTCAGCAAAGG | 8450 |
rs760903477 | snp | G/T | 3.52106e-05 | 0.00419572 | intron-variant | CUL4B | GRCh38.p7 | X:120545427 | ACAATCTTTTCATAT[G/T]TTTCTGGCATCCTTA | 8450 |
rs760938091 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120564030 | AGATCTGGCCACGCG[A/T]GGTGGCTCATGCCTG | 8450 |
rs760941322 | snp | C/T | 2.27907e-05 | 0.00337562 | missense | CUL4B | GRCh38.p7 | X:120574590 | CATCATCATTCCCAT[C/T]TCCTGATCCAGATGA | 8450 |
rs760980494 | snp | A/G | 7.13207e-05 | 0.0059712 | intron-variant | CUL4B | GRCh38.p7 | X:120526894 | AATGTAAAGTTCATT[A/G]TCATTGGCTCAAGCC | 8450 |
rs760983037 | snp | C/T | | | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120524951 | AATCTTGTGTAATAG[C/T]CTACATCTCACAGAC | 8450 |
rs761012081 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120531382 | GAACTGAAACCATCA[A/G]TTTCAGGATGCTGCA | 8450 |
rs761070624 | snp | A/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560750 | GGGAAGAAAGAAGAG[A/G]GGAGAAACACAGAGG | 8450 |
rs761072294 | in-del | -/TTC | 2.69027e-05 | 0.00366751 | intron-variant | CUL4B | GRCh38.p7 | X:120547258 | CAAGGTTAAAATACT[-/TTC]TTAAGGAGAGGATGA | 8450 |
rs761177136 | snp | C/G | 0.000228019 | 0.0106751 | synonymous-codon | CUL4B | GRCh38.p7 | X:120532551 | CAGAACTCTAGCTTT[C/G]CCACAGGCTAATGAC | 8450 |
rs761198038 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120571311 | ACTAAAAGGTTTTTT[A/T]AAAAAAAGTTTCAAG | 8450 |
rs761218654 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120569874 | GAATTAGCCAGGCAA[A/T]GGGAGTGAAAGGGAG | 8450 |
rs761219462 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120536256 | GCATTGGTTTCCTTC[A/C]CAGGTTCCTCTTTCT | 8450 |
rs761301526 | snp | C/T | 0.00158814 | 0.0281345 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561020 | GGGGAGAGGCTGTGG[C/T]TGGGGGAAAGGGGGA | 8450 |
rs761320364 | snp | C/T | 2.28009e-05 | 0.00337638 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560061 | TCCTTATTAGGTGAT[C/T]ATGGATTTTGGCCTT | 8450 |
rs761365165 | snp | C/T | 2.291e-05 | 0.00338445 | synonymous-codon | CUL4B | GRCh38.p7 | X:120526842 | AGATTCTATTCTCTT[C/T]TTAAGATCAGCAGGC | 8450 |
rs761381000 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120537662 | AGGAAAATCTAATTT[G/T]CCATCATTATCACCT | 8450 |
rs761391848 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120569090 | CGGCAATGCACATTT[A/T]AGGATATGGTGGCAA | 8450 |
rs761408490 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120545929 | ATATAAGGTATAAAC[C/T]AGATTAAGAAAAATG | 8450 |
rs761414854 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | CUL4B | GRCh38.p7 | X:120545108 | TACTATTCTATTTTC[A/G]TGTATACATGGACTT | 8450 |
rs761432629 | snp | C/T | 2.28172e-05 | 0.00337759 | synonymous-codon | CUL4B | GRCh38.p7 | X:120534575 | AAGAGAGACCTGGAG[C/T]TCCTTTTTACCCTGT | 8450 |
rs761544255 | snp | C/T | 2.29295e-05 | 0.00338588 | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560307 | ATCTTCGCATCAAAC[C/T]CTACAAACTCCAGGG | 8450 |
rs761561065 | snp | C/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120551251 | TTGCTCTGTCGCCCA[C/G]ATTGGGGTGCAATCT | 8450 |
rs761570341 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120528579 | CACAAAAATTAGCCA[A/G]GCGTGATTGTGCGCA | 8450 |
rs761600558 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120541209 | ATTCCCTTAAAAGAA[C/T]TGGATCAAGTCCGGG | 8450 |
rs761622877 | snp | A/G | 2.29742e-05 | 0.00338919 | missense | CUL4B | GRCh38.p7 | X:120540429 | TCAAATGCTTCTTTC[A/G]TGGCATTGATAAATT | 8450 |
rs761655034 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120553674 | TTTGGGAGGCCAAGG[C/T]GGGATGACTGCTTGA | 8450 |
rs761681301 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120566177 | CAATGGGCTGCTGAG[A/G]AGGCCAAAGCTCAAG | 8450 |
rs761683202 | snp | C/G | 0.000529661 | 0.016265 | utr-variant-5-prime | CUL4B | GRCh38.p7 | X:120575564 | ATGTGTATTTAACAC[C/G]TTCCGGGATGATAGA | 8450 |
rs761739716 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120531266 | GGCGGAGGCTGCAGT[A/G]AGCCAAGATCGTGCC | 8450 |
rs761809709 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120564614 | CTGTCTCAAAAAAAA[A/C]CAAAAACCTTCCAAG | 8450 |
rs761840212 | snp | A/G | 3.71678e-05 | 0.00431075 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120557889 | CCCACCTCAATTTAT[A/G]TTAATCAAATCTGGT | 8450 |
rs761899724 | snp | C/T | | | missense | CUL4B | GRCh38.p7 | X:120542995 | GCTGTTAAGTGTTCA[C/T]CTAGAAGTTGTTTTT | 8450 |
rs761902157 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120526286 | GGGAAATCACAAAAC[A/G]GGTGAACAACCAAGT | 8450 |
rs761945857 | snp | A/G | | | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120563421 | TTTGTATTTTTAGTA[A/G]AGTCAGGGTTTTGCT | 8450 |
rs761981721 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120548693 | ACAAAAATTAGCCGG[A/G]CATGGTGGTGCACGC | 8450 |
rs761994963 | snp | C/T | 2.27949e-05 | 0.00337593 | missense | CUL4B | GRCh38.p7 | X:120535868 | CACAGTGTCCTAGGG[C/T]TGACTGCCACTGAAG | 8450 |
rs761996170 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120559445 | TAGTGATGGAAAAAA[C/T]AGATGTAGTAATTGT | 8450 |
rs761998146 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120547953 | AACCTGGCTCTCCTT[A/G]CTCCTCAGCTTGCAG | 8450 |
rs762086062 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558152 | TGTGATCTTTATAAC[C/T]ATTACACCTAATCAT | 8450 |
rs762094686 | in-del | -/A | 0.00777442 | 0.0618609 | intron-variant | CUL4B | GRCh38.p7 | X:120545526 | CATGATCTGCCAATG[-/A]AAAAAAAAAGAAATC | 8450 |
rs762272681 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120529454 | ATAAGAACCCTAATA[A/G]CTAGCAGTCTATTCA | 8450 |
rs762303712 | snp | G/T | 2.30152e-05 | 0.00339221 | intron-variant | CUL4B | GRCh38.p7 | X:120544437 | GGGGAAAAAAAACTA[G/T]GATAGCAATCAGCTC | 8450 |
rs762432016 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120538417 | CTTATCTACTATTTA[A/G]GTATAAAATAAATGG | 8450 |
rs762494979 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120527324 | CAGCCTCCCAAAGTG[C/T]TGGGATTACAGGGAT | 8450 |
rs762513660 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120550825 | TGATGGAGCAATCTC[A/G]TAATAGGTATAAATA | 8450 |
rs762519216 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558369 | CATGTGTAAAACCTA[A/G]GTCGACATGAATTTT | 8450 |
rs762556831 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120536281 | TTTCTACCATCTGCC[-/A]AAATGTGAGCCTTTT | 8450 |
rs762628900 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120571839 | CAGGATTGGAAACCT[A/G]TAAAGGGAAGGCCAA | 8450 |
rs762645497 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120570069 | CTCAAGTCTGGTACA[A/G]CAATCTTAGGCCTCT | 8450 |
rs762670443 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120532215 | TAAACAAAGTAAGAT[A/G]TGAAACTATGTTGAG | 8450 |
rs762674517 | snp | A/G | 7.63728e-05 | 0.00617904 | intron-variant | CUL4B | GRCh38.p7 | X:120538248 | ATAATATTTTAAAGT[A/G]GTAAAAACAAAAGAG | 8450 |
rs762684071 | snp | A/C | 0.000250869 | 0.011197 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560048 | CTCGAGTGTCAAATC[A/C]TTATTAGGTGATTAT | 8450 |
rs762716786 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120549221 | GTAGTTAGAAGTCAC[A/G]TTCCCAATATGCAGG | 8450 |
rs762718166 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120546745 | TGGCACTTGATTATG[A/C]ACCAAAGTGCTATTT | 8450 |
rs762867830 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120573261 | TTAATATATATTAGA[A/G]ATCTGTCCATGACAG | 8450 |
rs762870023 | snp | C/T | 0.00158814 | 0.0281345 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120576677 | TACATGGTAGAGACC[C/T]GACATGGCTACTAAT | 8450 |
rs762873446 | snp | C/T | 3.76854e-05 | 0.00434065 | intron-variant | CUL4B | GRCh38.p7 | X:120539219 | TTGCTAGCTTCTCTG[C/T]TGAGTGCTATTTTAA | 8450 |
rs762876614 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120529649 | TTCAAAAAGATGCTT[A/C]ATCATGACTAGTTAT | 8450 |
rs762895092 | in-del | -/AT | | | intron-variant | CUL4B | GRCh38.p7 | X:120545843 | TGCCTTACATTGCAC[-/AT]GTGAGGGTTTTTATT | 8450 |
rs762918169 | snp | G/T | | | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120526669 | TTCATTTGGTCATCG[G/T]TAGTAAAAAAGGAGT | 8450 |
rs762918613 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120541454 | CAGCGAGCTAAGATC[A/G]TGCCACCGCACTCCA | 8450 |
rs762985994 | in-del | -/T | | | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120577617 | AAAAAAAAAAAAAAG[-/T]TTTTTTTCTATTCTC | 8450 |
rs762996305 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120565124 | CTTTTTGATCACAGG[G/T]ATTCCCCAGGGTGCT | 8450 |
rs763062130 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120574242 | TTTGAGAGGGAGTCT[C/T]GATCTGTCACCCAGG | 8450 |
rs763062564 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120539703 | TGTAATCCAAGCCAC[A/G]AAAAGACATGAGGAA | 8450 |
rs763068636 | snp | A/G | 3.24317e-05 | 0.00402676 | intron-variant | CUL4B | GRCh38.p7 | X:120546665 | TGGTACAAGTCATAT[A/G]TGCCATGTGACAGAG | 8450 |
rs763101374 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120528332 | GAATTGCTTGAACCC[A/G]GGAGGTGGAGGTTGT | 8450 |
rs763150542 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120538519 | ACAATAAGTTGGAAA[C/T]CTCAGGAGCTTGCTC | 8450 |
rs763154580 | snp | C/T | 0.000113327 | 0.00752667 | intron-variant | CUL4B | GRCh38.p7 | X:120545554 | ATCAAACAAGTTTTG[C/T]ATGTTGTGAAGCTGA | 8450 |
rs763226297 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120546058 | AATAAGAGTGACAGA[C/T]GAAATGTAGCTTTTT | 8450 |
rs763226397 | snp | A/G | 0.000529661 | 0.016265 | downstream-variant-500B | CUL4B | GRCh38.p7 | X:120524513 | AAAATAACAAAATCA[A/G]CAAATGTGAGTTCAT | 8450 |
rs763232075 | in-del | -/T | | | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120525883 | AAACTAGTTGCAAAG[-/T]TTTTTGCTCCTGTAA | 8450 |
rs763234798 | snp | C/T | 0.000102354 | 0.00715308 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561343 | TCCTTAACGGTCCCG[C/T]GGGAAGCTTCGCGCC | 8450 |
rs763261887 | snp | A/G | 2.27962e-05 | 0.00337603 | intron-variant | CUL4B | GRCh38.p7 | X:120535817 | ACTAAAAGTTTTGGG[A/G]ACATCCACTTACCTC | 8450 |
rs763284022 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120564427 | CCTGGCCAACATGGT[G/T]AAACCCTATCTCTAC | 8450 |
rs763311316 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120548746 | GGCTGAGGCAGGAGA[A/C]TTGCTTGAACCCAGG | 8450 |
rs763355711 | snp | C/T | 2.65866e-05 | 0.0036459 | intron-variant | CUL4B | GRCh38.p7 | X:120542955 | TCTCTTATTTACAAA[C/T]TGCCAATTACCTTTC | 8450 |
rs763376988 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120569271 | AGTATACAAAGACAA[C/T]CCTTGCCCTCCATTC | 8450 |
rs763436100 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CUL4B | GRCh38.p7 | X:120561440 | GTCCGCAGGACTTGA[G/T]TGGGGGGGGGAAGGG | 8450 |
rs763462970 | snp | C/T | 2.28318e-05 | 0.00337867 | synonymous-codon | CUL4B | GRCh38.p7 | X:120536945 | TGGTGGTAAATGAAC[C/T]TCCATAGGCACATAT | 8450 |
rs763576382 | in-del | -/CT | 0.0026455 | 0.0362733 | intron-variant | CUL4B | GRCh38.p7 | X:120533758 | AAGTGTCATTTCCCC[-/CT]TTCCCTATGGTTATA | 8450 |
rs763636143 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120568210 | CAATAGGGAGTGGTG[A/G]GAGGTGAGGTTACCA | 8450 |
rs763671355 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120534390 | AAACTCAAAACAGTT[A/C]TGAGGCAAGGAATTA | 8450 |
rs763692058 | snp | A/G | 2.56171e-05 | 0.00357881 | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558012 | TGCCAGGTTTCATCT[A/G]TGTAGTTTTCTGGTA | 8450 |
rs763725956 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120567601 | CTCTTGGCCAGGTGC[A/G]GTGGCTCATGCCTGT | 8450 |
rs763751924 | snp | A/C | 2.28066e-05 | 0.0033768 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560051 | GAGTGTCAAATCCTT[A/C]TTAGGTGATTATGGA | 8450 |
rs763761626 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120539889 | CAGAGGACCCTAGAC[C/T]TTCTCAGGTTACCTC | 8450 |
rs763762921 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120545003 | GCTTATTTGGTTATT[C/T]ATCAACTGGTTTCAA | 8450 |
rs763781389 | snp | G/T | 2.2847e-05 | 0.00337979 | missense | CUL4B | GRCh38.p7 | X:120543752 | GATCTAAGTAAGTAA[G/T]AAGTCTGTCTGCTTC | 8450 |
rs763806215 | multinucleotide-polymorphism | CTCGGATTACAGACACGTG/GACACGTGCCACCACACCT | | | intron-variant | CUL4B | GRCh38.p7 | X:120552279 | TAGCCTTCCCAGTAG[lengthTooLong]CCACCACACCTGGCT | 8450 |
rs763806839 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120571887 | TTCCGCAGAGCTGAC[C/T]GTGGGAGTTGAATAT | 8450 |
rs763815115 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120550707 | AGGTCAAGTTCGGAG[A/G]GAACATTCTGTTTTT | 8450 |
rs763868030 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120553502 | TTCATCAGAATTGAA[A/G]TATGGCCTAGGCTTG | 8450 |
rs763881116 | snp | A/G | 1.64914e-05 | 0.00287149 | intron-variant | CUL4B | GRCh38.p7 | X:120538255 | TTTAAAGTGGTAAAA[A/G]CAAAAGAGGTTTAAA | 8450 |
rs763893940 | snp | C/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120549269 | CAAATGAAAAGAAAG[C/G]TTGGCAGAGCGCGGT | 8450 |
rs763939325 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120573444 | CATAAATCTGTGCAT[A/G]TATAAAAGTATTTCT | 8450 |
rs763954965 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560960 | GAGCGACTCAGCGAG[C/T]CTGTGAGGCTGCAGC | 8450 |
rs763976628 | snp | A/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120528503 | GGCTGTGGGCAGATC[A/T]TGAGGTCAGGAGTTC | 8450 |
rs763981937 | snp | C/T | | | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120526738 | CTACTGCATATGACA[C/T]CAAATGCTGCAAGGC | 8450 |
rs763995178 | snp | A/G | 3.73051e-05 | 0.0043187 | intron-variant | CUL4B | GRCh38.p7 | X:120539228 | TCTCTGTTGAGTGCT[A/G]TTTTAAAAGAAAAAT | 8450 |
rs764004283 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120538964 | TCTTTATTGTAAAAC[-/T]TTTTTGCATGTAACT | 8450 |
rs764022849 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120548847 | TCAAAAAGGAATAAA[A/T]TAAAAAATAAATAAA | 8450 |
rs764044610 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, utr-variant-5-prime | CUL4B | GRCh38.p7 | X:120559889 | AAACACCCGGTGTAT[A/G]CTTCAGCACAAGGAT | 8450 |
rs764048432 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120547917 | GAACATCAGACTCCA[A/G]GTTCTTCAGTTTTGG | 8450 |
rs764049053 | snp | A/C | 0.000529661 | 0.016265 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120524966 | TCTACATCTCACAGA[A/C]CATCAGGGATGAGTT | 8450 |
rs764061992 | snp | A/C | 0.000113952 | 0.0075474 | missense | CUL4B | GRCh38.p7 | X:120574605 | CTCCTGATCCAGATG[A/C]CTGTGACATCATCCG | 8450 |
rs764079978 | snp | C/T | | | downstream-variant-500B | CUL4B | GRCh38.p7 | X:120524194 | TTGAGGAACATCTTA[C/T]TCTGAGAGTATCTGG | 8450 |
rs764182117 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120538408 | TGTAGTAACCTTATC[C/T]ACTATTTAGGTATAA | 8450 |
rs764197401 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120570452 | GGCTGCTTTTATGCT[A/G]AAACAGCAGAGTTTA | 8450 |
rs764241197 | snp | A/G | 3.29592e-05 | 0.00405938 | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560556 | GGCGGAGTGGTGCTG[A/G]TATTACCATCAGTGG | 8450 |
rs764272638 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120532644 | CAGCATGAACAACTA[C/T]GACATTCTACCTCAA | 8450 |
rs764332387 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | CUL4B | GRCh38.p7 | X:120532166 | TTCGAAGCTATTTAA[C/T]GGCATGGAAAAATTC | 8450 |
rs764382485 | snp | A/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120542852 | ATTGTGTCCATCCTC[A/T]GAAATGCAGCCACAT | 8450 |
rs764431873 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120556444 | AGATTATAGTGCCTG[A/G]AGGCGTTTTCCACAA | 8450 |
rs764434013 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120566582 | TTGTGTTTTTAGTAG[A/G]GACGGGGTTTCTCCA | 8450 |
rs764435835 | snp | G/T | 3.40698e-05 | 0.0041272 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561344 | CCTTAACGGTCCCGC[G/T]GGAAGCTTCGCGCCG | 8450 |
rs764466763 | snp | C/T | 2.27959e-05 | 0.00337601 | intron-variant | CUL4B | GRCh38.p7 | X:120535823 | AGTTTTGGGAACATC[C/T]ACTTACCTCTTTAAA | 8450 |
rs764508431 | in-del | -/T | 0.00370173 | 0.0428621 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120563228 | GAATATACCACATAG[-/T]TTTTTTCATTTTGTT | 8450 |
rs764525237 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120571312 | CTAAAAGGTTTTTTT[A/T]AAAAAAGTTTCAAGA | 8450 |
rs764531724 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120527648 | TTCATCTATGTTTCA[A/T]ACATACCTTACATAG | 8450 |
rs764543744 | snp | A/T | 0.000137207 | 0.00828159 | intron-variant | CUL4B | GRCh38.p7 | X:120543706 | AGTTTAAGACTATTA[A/T]ATTCAGCATGTGGTA | 8450 |
rs764580798 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120571915 | TATGCACCGATTTTG[A/G]TATCTGCAGGGTTCC | 8450 |
rs764633997 | snp | A/T | 0.000106113 | 0.00728323 | intron-variant | CUL4B | GRCh38.p7 | X:120542956 | CTCTTATTTACAAAT[A/T]GCCAATTACCTTTCT | 8450 |
rs764653865 | snp | C/T | 2.72216e-05 | 0.00368918 | intron-variant | CUL4B | GRCh38.p7 | X:120542947 | AAAAGCAATCTCTTA[C/T]TTACAAATTGCCAAT | 8450 |
rs764677395 | snp | C/T | | | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120576365 | TTTTTATAACAAATA[C/T]TGGAAAATAAAAGGG | 8450 |
rs764685909 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120533428 | CAGGCCCTACTCATC[G/T]TACCTAATTTTTTAA | 8450 |
rs764704246 | snp | C/G | 0.00105904 | 0.0229869 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561070 | TGTTATTGTCAATAG[C/G]ACAAGAGGCTAAAGA | 8450 |
rs764733784 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120554554 | TTGCTTACTGCAAGT[A/G]TACTTAGAACAGCAT | 8450 |
rs764820525 | in-del | -/ATAC | 0.000529661 | 0.016265 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120526327 | TTTTCTATTTGATAA[-/ATAC]ATCCAGAACTCTGTA | 8450 |
rs764823825 | snp | A/T | 2.46697e-05 | 0.00351202 | intron-variant | CUL4B | GRCh38.p7 | X:120547126 | CGATTTTTTGTTTTA[A/T]AAAGGATATTCTCTG | 8450 |
rs764912137 | snp | A/T | 0.000529661 | 0.016265 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120525373 | AACAAACATAAACAA[A/T]ATTTTCTGCTTCTCC | 8450 |
rs764912964 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120531485 | TTCTTTTTTTTAAAC[A/G]GAGTCTCACTGTCAC | 8450 |
rs764939960 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560005 | TCCAAACTGTTTAAT[A/G]TATTAACATAAATAG | 8450 |
rs764967931 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120571485 | GATGCACCCTCCAAC[C/T]TGGTGGAAGAATGGA | 8450 |
rs764975012 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | CUL4B | GRCh38.p7 | X:120545162 | CTCTTGATGGTCAGC[A/G]GCAAAATGAATCACA | 8450 |
rs764984967 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-5-prime | CUL4B | GRCh38.p7 | X:120575595 | CTGCAGGGCTGACCA[A/G]TCTCTGCAGGGGAAA | 8450 |
rs765018068 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120569291 | GCCCTCCATTCTCAA[C/T]TGGCAATGTAGGTTT | 8450 |
rs765025052 | snp | C/T | 2.81452e-05 | 0.00375124 | synonymous-codon, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120557939 | CTGGTAGAGTTCTTC[C/T]AAATTGTACTTAATT | 8450 |
rs765076513 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120541315 | GGCCAGCCTGACCAA[A/C]ATGGTGAAACCCCGT | 8450 |
rs765098993 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120540204 | TGTGGGCTTTCAGTA[C/T]TTACATCCAGGTTTT | 8450 |
rs765147276 | snp | C/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120546786 | AAAAGAAAAAAAAAA[C/G]ATAGTTTATACTAAA | 8450 |
rs765203891 | in-del | -/A | 0.0026455 | 0.0362733 | intron-variant | CUL4B | GRCh38.p7 | X:120538477 | ACAATGCTTTATCTT[-/A]AAAAAAAACAACTCT | 8450 |
rs765242771 | in-del | -/TAAGA | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561825 | GGAATGTCCCTATGT[-/TAAGA]TAGGAAAGGAGAAGA | 8450 |
rs765309077 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120548997 | GTAAGTTTCCTGTTA[C/T]GCATATATAAAAGAC | 8450 |
rs765343926 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120572303 | ACCCTGTCTTTACTT[A/T]AAAAATATAAAATTA | 8450 |
rs765400948 | snp | C/T | 4.586e-05 | 0.00478831 | missense | CUL4B | GRCh38.p7 | X:120544534 | AACTTCTATCAATTG[C/T]TTCACCATTCCTTTC | 8450 |
rs765416325 | in-del | -/TTTTAT | 0.00211696 | 0.0324653 | intron-variant | CUL4B | GRCh38.p7 | X:120537897 | CTTCAGTTCAATACA[-/TTTTAT]TTTTATTTTTATTTT | 8450 |
rs765424130 | snp | A/C | | | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120559205 | ACTTCTCTATTTAAT[A/C]AACACTGTAGCACTG | 8450 |
rs765432282 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120571365 | GGCAGACCATGACAG[C/T]ATGCAGAAAGAATAG | 8450 |
rs765465776 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120538016 | TCACCTCAGTTGCCA[C/T]GAATTACAACAAACA | 8450 |
rs765512268 | snp | A/G | | | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561049 | GAGGGGGAAAGAACC[A/G]GGGCTTGTTATTGTC | 8450 |
rs765543535 | snp | A/G | 2.27944e-05 | 0.00337589 | missense | CUL4B | GRCh38.p7 | X:120530130 | TTCAACTGGTTGTAC[A/G]CTTCTGAAACAAGGA | 8450 |
rs765570708 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120543906 | GGCCCTGTCAAATGT[C/G]ACAGGGTAGAATCAT | 8450 |
rs765577289 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558176 | TAATCATTAAAGTAA[C/T]CACTGTATTTAAGCT | 8450 |
rs765596891 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120553759 | TTAAACAAAACAAAA[C/G]AAAACACTGCGGCTA | 8450 |
rs765601942 | snp | G/T | 1.80706e-05 | 0.00300582 | synonymous-codon | CUL4B | GRCh38.p7 | X:120545515 | AATGCTCCTGATCAT[G/T]ATCTGCCAATGAAAA | 8450 |
rs765609729 | snp | C/T | 3.42343e-05 | 0.00413714 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561340 | CCCTCCTTAACGGTC[C/T]CGCGGGAAGCTTCGC | 8450 |
rs765728839 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120565059 | TACAATGTCAATTCC[C/T]TTATTTCTGTGGACA | 8450 |
rs765740839 | snp | G/T | | | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120576089 | TTAGCTATCTAAAAT[G/T]TTCTCGATTGCTAGA | 8450 |
rs765755721 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | CUL4B | GRCh38.p7 | X:120564363 | GTAATCCCAAAACTT[C/T]GGGAGGCTGAGGCGG | 8450 |
rs765769140 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120574675 | CCAGCAGTCCTCTCC[C/G]ATATCTGTATAGTGT | 8450 |
rs765809665 | snp | A/G | 2.70179e-05 | 0.00367535 | synonymous-codon, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560540 | CTTCTTGGCAGAGGT[A/G]GGCGGAGTGGTGCTG | 8450 |
rs765830120 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120574329 | CATTCTCCTGCCTAA[A/G]CCTCCTGAGTAGCTG | 8450 |
rs765830798 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120554297 | CTTAGAGAAGTAACT[C/T]GCCCAAAGTTATATG | 8450 |
rs765846371 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120551508 | GCCACCCGATTATAA[A/C]CTTTCACACATCCTT | 8450 |
rs765940707 | snp | A/T | 0.00105904 | 0.0229869 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561950 | CTGAATAAGGCCTGA[A/T]TTTTGATGCCTTTCT | 8450 |
rs766008370 | snp | C/G | 0.000529661 | 0.016265 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120526446 | TAAGAACCCTCCCCC[C/G]TTTTTAATAGCCACA | 8450 |
rs766068198 | snp | A/G | 0.00317376 | 0.039709 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561203 | GCGCGTGAGGGGGCG[A/G]CTGGAAAGGGGCGGC | 8450 |
rs766127119 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120567299 | CAGCTAAATTTTTTG[A/G]TATTTTTAGTAGAAA | 8450 |
rs766152597 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120533218 | CTCCATTTTCATGGT[C/T]TCATTCTAGTCTAAG | 8450 |
rs766188101 | snp | G/T | 6.83924e-05 | 0.00584735 | missense | CUL4B | GRCh38.p7 | X:120535883 | TTGACTGCCACTGAA[G/T]TTTCCTGCCACTATG | 8450 |
rs766196936 | snp | A/C | 2.60014e-05 | 0.00360555 | intron-variant | CUL4B | GRCh38.p7 | X:120540566 | GCTGCCAAATGCCTA[A/C]AACAAAAAATTACCA | 8450 |
rs766230552 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120532221 | AAGTAAGATATGAAA[C/T]TATGTTGAGTATCAT | 8450 |
rs766251049 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120531563 | ATCCCGGGTTCAGGT[A/G]ATTCTCATGCCTCAG | 8450 |
rs766251177 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120542632 | TTTTATTTAAAGAGA[C/T]GAGAGTCTCACTATG | 8450 |
rs766278242 | snp | C/T | 2.55366e-05 | 0.00357318 | intron-variant | CUL4B | GRCh38.p7 | X:120547119 | CTATTCACGATTTTT[C/T]GTTTTAAAAAGGATA | 8450 |
rs766326122 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120566661 | CTCAGCTTCCCAAAG[C/T]GCTGGGATTACAGGT | 8450 |
rs766335088 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120541457 | CGAGCTAAGATCGTG[A/C]CACCGCACTCCAGCC | 8450 |
rs766473405 | snp | A/C | 4.592e-05 | 0.00479144 | intron-variant | CUL4B | GRCh38.p7 | X:120544461 | TCAGCTCTGTATAGT[A/C]GGTGTAGTAGTTAAC | 8450 |
rs766490306 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120568788 | TCAGCAAAGGAAGTT[A/C]AAATTATTTGCTAAA | 8450 |
rs766506778 | snp | C/T | | | splice-acceptor-variant | CUL4B | GRCh38.p7 | X:120546617 | CTATCCAATGAATCC[C/T]TGAAACATATGTTAA | 8450 |
rs766513783 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120572340 | TGTGGTGGCGCATGC[C/T]TATAATCCCAGCTAC | 8450 |
rs766516618 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120565137 | GGGATTCCCCAGGGT[A/G]CTTGGGGAATCAAGA | 8450 |
rs766543340 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120530580 | CTTTGATATATCTTC[C/T]AAATGTGTGTATCAG | 8450 |
rs766565813 | snp | G/T | 0.000819857 | 0.0202301 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CUL4B | GRCh38.p7 | X:120561449 | ACTTGAGTGGGGGGG[G/T]GAAGGGGGGAGGGAG | 8450 |
rs766568315 | snp | A/C | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560758 | AGAAGAGAGGAGAAA[A/C]ACAGAGGACGAGAAG | 8450 |
rs766585490 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558960 | TATTGACTTCAGAAA[A/G]CTCTACTATTAAATC | 8450 |
rs766633596 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120529764 | ATACCATGGTATTTC[A/T]ATAAATACCATGGTA | 8450 |
rs766667388 | snp | C/T | 4.57091e-05 | 0.00478042 | intron-variant | CUL4B | GRCh38.p7 | X:120530058 | ATCTAATGTACTTTC[C/T]TTTATTTATAACACG | 8450 |
rs766676053 | snp | C/T | 2.49622e-05 | 0.00353277 | intron-variant | CUL4B | GRCh38.p7 | X:120543843 | ACATTATTGTTTTCC[C/T]CCCCATAAATCATTC | 8450 |
rs766735343 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120535412 | ACAATTATAAAACAA[C/T]AGCTTAAACTGGCCA | 8450 |
rs766761887 | in-del | -/CA | | | intron-variant | CUL4B | GRCh38.p7 | X:120529544 | AGGCCAGTACAACAT[-/CA]CACATTAAGTGACTT | 8450 |
rs766807832 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120556170 | CGCATATATAATACG[C/T]CAAAAGAGCCATATG | 8450 |
rs766869446 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120536260 | TGGTTTCCTTCACAG[A/G]TTCCTCTTTCTACCA | 8450 |
rs766883719 | in-del | -/GAG | | | cds-indel, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560262 | GCAGTTGGTGAAGAT[-/GAG]GAGGAGGAGGAGGAG | 8450 |
rs766905031 | snp | A/C | 0.00370173 | 0.0428621 | intron-variant | CUL4B | GRCh38.p7 | X:120532366 | TCTTTATATATTTTG[A/C]TTATTAACATGTATA | 8450 |
rs766965938 | snp | C/G | 2.2842e-05 | 0.00337942 | missense | CUL4B | GRCh38.p7 | X:120532578 | TGACTGCAGTGTTCT[C/G]CTTAACTCTCCATCC | 8450 |
rs766973308 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120576863 | ATTATGATTATGATG[C/T]TATGATTAGTCCATC | 8450 |
rs766991083 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120542773 | TGGATCCCTCTCTTC[C/T]AGTTCCTGTATCTTT | 8450 |
rs767122119 | snp | A/G | 2.28825e-05 | 0.00338242 | intron-variant | CUL4B | GRCh38.p7 | X:120538649 | AGGAACAGAAAGAAT[A/G]AGAAACCTACCATGT | 8450 |
rs767130550 | snp | A/C | 0.00105904 | 0.0229869 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120576005 | TAGGCTCCTGTTCCG[A/C]CATTGCTGGCTTGGG | 8450 |
rs767130883 | snp | C/T | 2.27975e-05 | 0.00337612 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560070 | GGTGATTATGGATTT[C/T]GGCCTTGGTTACCTT | 8450 |
rs767132788 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120573829 | CTTCCTTTTCTTTTT[C/T]CTTTTCTTTTTTTTG | 8450 |
rs767178271 | in-del | -/AG | | | intron-variant | CUL4B | GRCh38.p7 | X:120532607 | CTCTGAAGAAGAAAC[-/AG]AGAGGTTTAGTTATT | 8450 |
rs767224410 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120551345 | TGGGATTACAAGCAT[A/G]CGCCGCCACACTCAG | 8450 |
rs767244628 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120531448 | AAACAAAATATTCAC[C/T]TTCCCTGTTTTTGTT | 8450 |
rs767304838 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120551162 | TTTTAGCATGGTGTT[A/C]AAGGCAAATCTTACC | 8450 |
rs767327472 | snp | C/T | 2.29289e-05 | 0.00338584 | synonymous-codon, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560309 | CTTCGCATCAAACCC[C/T]ACAAACTCCAGGGTG | 8450 |
rs767397218 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120548216 | GAGTTCAAGGTTGAA[G/T]TGAACCATGACTACG | 8450 |
rs767428541 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120541385 | ATGCCTGTAATCCTA[A/G]CTACTTGGGAGGCTG | 8450 |
rs767435258 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120568171 | TAGGAGACTGGAGGT[A/G]AACAGAACTAGAAGA | 8450 |
rs767483091 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558616 | TGGAAACATCTTAAC[C/T]CAGGTTTTAAACTAC | 8450 |
rs767564735 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120564853 | CTAAACCAGACTGGG[C/T]ACTTAACACATATTC | 8450 |
rs767643114 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120565472 | GTGGATCACTTGGCC[A/G]GGAGTTTGAGACCAG | 8450 |
rs767652998 | snp | A/T | 4.59849e-05 | 0.00479483 | intron-variant | CUL4B | GRCh38.p7 | X:120537037 | GATTCTGCATATACT[A/T]TAAGAAGATCAAAAC | 8450 |
rs767675993 | in-del | -/T | 2.54774e-05 | 0.00356904 | intron-variant | CUL4B | GRCh38.p7 | X:120547121 | ATTCACGATTTTTTG[-/T]TTTAAAAAGGATATT | 8450 |
rs767678634 | snp | C/T | 2.52286e-05 | 0.00355157 | synonymous-codon | CUL4B | GRCh38.p7 | X:120542982 | TTTCTGAAGAATTGC[C/T]GTTAAGTGTTCACCT | 8450 |
rs767681352 | in-del | -/TGAG | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120556301 | TGTTGTGCACTGATT[-/TGAG]TATTTTGCGTGTACT | 8450 |
rs767686569 | in-del | -/A | | | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120557826 | AATTAGAAGGGAACC[-/A]AAAAGTCTACTTAAG | 8450 |
rs767705547 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120531271 | AGGCTGCAGTGAGCC[A/G]AGATCGTGCCACTGA | 8450 |
rs767739503 | in-del | -/ATTCCCACCAA | | | intron-variant | CUL4B | GRCh38.p7 | X:120568526 | TACTAAATGTCCTTT[-/ATTCCCACCAA]ATTCCCACCAACAGC | 8450 |
rs767820716 | snp | C/G | 3.30846e-05 | 0.00406709 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561363 | AGCTTCGCGCCGCAG[C/G]GCCCTTACCGGAAGT | 8450 |
rs767875072 | snp | C/T | 2.29043e-05 | 0.00338402 | missense | CUL4B | GRCh38.p7 | X:120543781 | TCTTCTTCTAGACGT[C/T]TGTTAACATGATGTA | 8450 |
rs767894984 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120570240 | AAGCGGGAGAATAGG[A/G]TTTGACACGTGCAAA | 8450 |
rs767936313 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120536665 | AACATTAAAGCAGTT[G/T]GTATTTGGTGTTGGT | 8450 |
rs767985470 | snp | C/T | 0.00011868 | 0.00770234 | intron-variant | CUL4B | GRCh38.p7 | X:120526892 | TCAATGTAAAGTTCA[C/T]TATCATTGGCTCAAG | 8450 |
rs768030859 | snp | C/T | 0.00370173 | 0.0428621 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120562350 | AAACCTTGTAAATTC[C/T]CTGTTGGGAGTTTTT | 8450 |
rs768040744 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | CUL4B | GRCh38.p7 | X:120546320 | AAATCTTACAAATCA[C/T]CACTAAGGAACTTAC | 8450 |
rs768071363 | snp | G/T | 2.29872e-05 | 0.00339014 | intron-variant | CUL4B | GRCh38.p7 | X:120544440 | GAAAAAAAACTAGGA[G/T]AGCAATCAGCTCTGT | 8450 |
rs768134389 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120554632 | CACTAGGGACTTCCA[C/T]ACTTAAAGCTTTAAA | 8450 |
rs768169531 | snp | C/T | 2.75239e-05 | 0.00370961 | intron-variant | CUL4B | GRCh38.p7 | X:120544233 | AAATGAAGGAGATCA[C/T]TTATTTAGCAAATAT | 8450 |
rs768175107 | snp | A/G | 5.92874e-05 | 0.00544428 | intron-variant | CUL4B | GRCh38.p7 | X:120532377 | TTTGATTATTAACAT[A/G]TATAATTCCAGTGTG | 8450 |
rs768200862 | snp | A/C | | | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558498 | ACTGAGGCTGGAACT[A/C]ATTTAGTAAGCTTGC | 8450 |
rs768220869 | snp | A/C/G | 2.27907e-05 | 0.00337562 | synonymous-codon, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560117 | TAACTTCTTAGCAGA[A/C/G]CCAGGTTTGCTGTTA | 8450 |
rs768224213 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120564978 | GGCCACCTTTAACCA[A/G]GCTGTTTATAAAGGT | 8450 |
rs768257858 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120545870 | TTATTGGCAGGGGGT[G/T]GGGGTGGGGAGGGGT | 8450 |
rs768278886 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120555696 | CCTGTAATCCCAGCA[C/T]CTTGGGAGGTGGAGG | 8450 |
rs768313033 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120537498 | AGGGAAGGAAAAAGA[A/G]GGGAAAAGGGCAAAG | 8450 |
rs768313041 | snp | G/T | | | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120562708 | GGCATTCTGGGGAAC[G/T]GAAACAAGGGCAAAG | 8450 |
rs768338680 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560280 | GAGGAGGAGGAGGAG[A/G]ATTCCTCAGCCATCT | 8450 |
rs768344589 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120526132 | TAGGATGTGAATATA[C/T]AAGATATTATGTAAG | 8450 |
rs768363837 | snp | G/T | 2.33904e-05 | 0.00341975 | missense | CUL4B | GRCh38.p7 | X:120544639 | ATAACTCCAGTCCCA[G/T]GTCCCTAAAATAAAA | 8450 |
rs768369622 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120573400 | CAATTTTTGTGACTA[C/T]AAACATGCTCCAATG | 8450 |
rs768408727 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120562707 | AGGCATTCTGGGGAA[C/T]GGAAACAAGGGCAAA | 8450 |
rs768412228 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120569651 | AGGCGTGAGCCACCG[C/T]GCCCGGCTGGGAAGT | 8450 |
rs768424127 | snp | A/C | 2.28191e-05 | 0.00337772 | missense | CUL4B | GRCh38.p7 | X:120526797 | GTTTGGATTTTCTTT[A/C]TCTCTTTCCATGTAG | 8450 |
rs768459791 | snp | C/T | | | utr-variant-5-prime | CUL4B | GRCh38.p7 | X:120575406 | GGCATTTTAGCTCAC[C/T]GTCAGTCACTGGAGG | 8450 |
rs768464875 | in-del | -/AG | 0.00475684 | 0.0485365 | intron-variant | CUL4B | GRCh38.p7 | X:120550612 | TGGGCTTTACAGCAC[-/AG]AGTCTCACCTGTGTT | 8450 |
rs768498652 | snp | C/G | 0.00158814 | 0.0281345 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561570 | GGTGGGGGGGGTGGC[C/G]GGAGGAGCGGGAAGG | 8450 |
rs768500892 | in-del | -/ACAA | | | intron-variant | CUL4B | GRCh38.p7 | X:120565352 | ATGCATTAAAAAAAC[-/ACAA]ACAACAACAAAAAGC | 8450 |
rs768580074 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120536013 | CCATTTTTATACTTA[C/T]CTCATGTGATATAGT | 8450 |
rs768605871 | snp | C/T | 2.3603e-05 | 0.00343525 | intron-variant | CUL4B | GRCh38.p7 | X:120540357 | CAACTGGAAAAAGGA[C/T]TGGAAAACATACCTA | 8450 |
rs768607173 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120569013 | GCTAAATCAAAATGC[C/T]CAAAAGGAGACCAAG | 8450 |
rs768618852 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120532256 | ATCCTGTACAACCAC[C/T]CTCCCAAACACCCAA | 8450 |
rs768626839 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120533356 | TTCCACCATGCCACA[C/T]AGTTGAGACACTACA | 8450 |
rs768697629 | snp | C/G/T | 6.99331e-05 | 0.00591291 | synonymous-codon, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560414 | GGTTGAAGGGGATGC[C/G/T]GAATCCCTGGGTTGT | 8450 |
rs768769282 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120534110 | TGCAGGGGCTCATGC[C/T]TGTAATTGCAGTACT | 8450 |
rs768817993 | snp | C/T | 0.00581083 | 0.0535878 | intron-variant | CUL4B | GRCh38.p7 | X:120543383 | AGGCCCCTCGACTGG[C/T]AATATTAATACTTAG | 8450 |
rs768824909 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120564468 | AAAATTATCTGGGCA[C/T]GTTGGCAGGTGCCTG | 8450 |
rs768894046 | snp | A/G | 3.21942e-05 | 0.00401199 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558082 | AGAATACCATGTCAG[A/G]TACAGTAACCAAAGA | 8450 |
rs768905107 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120567876 | AAGACTCTGAAGAAA[A/G]AAAAAAAAAACAGCT | 8450 |
rs768934084 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120567266 | GTAGCTGGGATTACA[A/G]GTGTGCACCACCATG | 8450 |
rs768947438 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120576542 | GGTTAACGTAACTGG[A/G]AAGAATAGGGCAGAT | 8450 |
rs768970682 | snp | C/T | 9.12971e-05 | 0.00675575 | missense | CUL4B | GRCh38.p7 | X:120536950 | GTAAATGAACTTCCA[C/T]AGGCACATATGTCGG | 8450 |
rs768989505 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120529224 | GGTAATGAGGAGTGC[A/G]ATATTAGGTTTGGAG | 8450 |
rs769059016 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120572867 | TTTCTCTTACCTTAC[G/T]TTGCTGGACTGACAA | 8450 |
rs769112172 | snp | A/G | 2.27925e-05 | 0.00337576 | synonymous-codon | CUL4B | GRCh38.p7 | X:120574555 | CATTTACTCACCACC[A/G]TCTTTAGAGGTAGTA | 8450 |
rs769133141 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120538350 | AAGAAATCCTTACCC[A/C]AAAGTGTATGCCCCA | 8450 |
rs769149609 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120548666 | TAGTGAAACCCCGTC[G/T]CCACTAAAAATACAA | 8450 |
rs769166770 | snp | A/G | 2.30936e-05 | 0.00339798 | missense | CUL4B | GRCh38.p7 | X:120538191 | CCTTCAAGTTTGCTG[A/G]TGAAAGCAGCTCCGC | 8450 |
rs769247744 | snp | C/T | 0 | 0 | downstream-variant-500B | CUL4B | GRCh38.p7 | X:120524180 | TGGGTTCAAAAACTT[C/T]GAGGAACATCTTACT | 8450 |
rs769288255 | snp | C/G | | | downstream-variant-500B | CUL4B | GRCh38.p7 | X:120524092 | TTTCTGAACTGTACA[C/G]TCACATACACAGCAA | 8450 |
rs769294903 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120544077 | AAGGTCTATTGTGAG[A/C]GACAGTGAGAATTTA | 8450 |
rs769318054 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120559329 | AAAATTGCTGATTTT[A/G]TATTTGCCTCAATGT | 8450 |
rs769348053 | snp | A/C/G | 7.77235e-05 | 0.00623352 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CUL4B | GRCh38.p7 | X:120561438 | AGGTCCGCAGGACTT[A/C/G]AGTGGGGGGGGGAAG | 8450 |
rs769364624 | in-del | -/T | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120555940 | TAGCAAGACTCCATC[-/T]CAAAAAAAAAAAAAA | 8450 |
rs769380598 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558347 | AACAATCCTGATCTT[A/G]TTTCATCATGTGTAA | 8450 |
rs769389134 | snp | A/T | 2.2798e-05 | 0.00337616 | intron-variant | CUL4B | GRCh38.p7 | X:120574538 | CTTGAGTTTTACTAG[A/T]TCATTTACTCACCAC | 8450 |
rs769406315 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120536192 | ATTCACCTGCAGCAG[C/G]TTTTGTGCCTCTGCA | 8450 |
rs769460836 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120537371 | CCCACCTTTGAATAC[C/T]CCTATGTGGCTTAAA | 8450 |
rs769464062 | in-del | -/TATATATATATAT | 0.00212033 | 0.032491 | intron-variant | CUL4B | GRCh38.p7 | X:120566376 | ATATATATATATATA[-/TATATATATATAT]ATGTATATATATTTG | 8450 |
rs769537833 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120535404 | TCTAGGATACAATTA[G/T]AAAACAACAGCTTAA | 8450 |
rs769540198 | snp | A/G | 2.36852e-05 | 0.00344122 | intron-variant | CUL4B | GRCh38.p7 | X:120543688 | TGCAAGTGATTTAAC[A/G]ACAGTTTAAGACTAT | 8450 |
rs769548548 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120552721 | GTAGCAAATGACATA[C/T]GCAAATATTTACTGA | 8450 |
rs769551196 | in-del | -/A | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120563010 | ATAAATCAACTTTCT[-/A]AACTTTGTTTAAACA | 8450 |
rs769606988 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120559774 | TTAGAATACAAATTT[A/C]TCACCTGCAAAATCC | 8450 |
rs769677249 | snp | A/G | 2.2805e-05 | 0.00337668 | synonymous-codon, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560267 | TGGTGAAGATGAGGA[A/G]GAGGAGGAGGAGGAT | 8450 |
rs769687230 | snp | G/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120563502 | TCAGCCTCCCAAAGT[G/T]CTGGGCCTACCATAT | 8450 |
rs769690134 | in-del | -/T | 7.92267e-05 | 0.00629342 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CUL4B | GRCh38.p7 | X:120561441 | TCCGCAGGACTTGAG[-/T]GGGGGGGGGAAGGGG | 8450 |
rs769730471 | snp | C/T | 4.56496e-05 | 0.00477731 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120526754 | CAAATGCTGCAAGGC[C/T]AACATTCTATGCAAT | 8450 |
rs769768844 | snp | G/T | 2.28105e-05 | 0.00337709 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560034 | AGAGCACGTGACCCC[G/T]CGAGTGTCAAATCCT | 8450 |
rs769812875 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120573095 | AAAGAAAAAATAAAA[C/T]TAAAAGTGTCTTTTA | 8450 |
rs769816347 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | CUL4B | GRCh38.p7 | X:120527185 | CTGCCTCAGCTTCCC[A/G]AGTAGCTGGGACTAG | 8450 |
rs769853976 | in-del | -/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120539448 | ATATATACCCAAAGA[-/G]GAGTATGATACACTG | 8450 |
rs769875122 | snp | A/T | 0.000529661 | 0.016265 | downstream-variant-500B | CUL4B | GRCh38.p7 | X:120524406 | ATCCACCTTGAGGAT[A/T]CCTGGGAATTTTCCT | 8450 |
rs769938750 | in-del | -/AACAACAT | | | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120525840 | AGACAAAACTGTCCA[-/AACAACAT]TTAAAGTCTAAAGTA | 8450 |
rs770000609 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120552837 | AGCTATGTTTACAGA[C/T]AGTAAGTAAAGCACA | 8450 |
rs770054334 | in-del | -/G | 0.00212089 | 0.0324953 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560782 | GAGAAGGAAAGTGAA[-/G]GGGGGGGGCTACACC | 8450 |
rs770072922 | snp | C/T | 0.00317376 | 0.039709 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120559475 | TTCCTATCTTTAGAC[C/T]AGTGGTACACAGAGT | 8450 |
rs770179680 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120564211 | AAATGGCTGAGGCAA[A/G]AGAATCCCTTGAACC | 8450 |
rs770191812 | snp | G/T | 0.00475684 | 0.0485365 | intron-variant | CUL4B | GRCh38.p7 | X:120565854 | CCTCAGCCTCCCAAG[G/T]AGCTGGGACTACAGG | 8450 |
rs770199279 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120530391 | GGGTCTTATAAATAT[A/G]GATGCTGACAGAGAA | 8450 |
rs770199645 | snp | A/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120573768 | CTACCTTGCTATTAA[A/T]TTTTTTATTAATTGT | 8450 |
rs770289640 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120540797 | CATGTACCACTGCAC[C/T]TGGCAAAATAAAGCT | 8450 |
rs770290973 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120539642 | TATGAAAATAGGATA[C/T]GGATATCCTGTGGGG | 8450 |
rs770295824 | snp | A/G | 4.68324e-05 | 0.0048388 | synonymous-codon | CUL4B | GRCh38.p7 | X:120547200 | TCAGCTGTTTGTACA[A/G]GTTTGCAGAAATCTT | 8450 |
rs770379482 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120550321 | AGCTTTGAACCAAGT[A/G]AATACATGAAGTATT | 8450 |
rs770443928 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120536416 | CCTTAATCCCTTTTA[A/T]GGGCTTCAGTCCTGG | 8450 |
rs770446020 | snp | C/G | 0.000352342 | 0.0132683 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CUL4B | GRCh38.p7 | X:120561428 | CGAAGCCCCCAGGTC[C/G]GCAGGACTTGAGTGG | 8450 |
rs770459009 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120528137 | TTAGACCGGGTGTGG[C/T]GGCTCATGCCTGTAA | 8450 |
rs770473227 | snp | A/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120545727 | TTTTCTAGAAAAAAG[A/T]CACTTAAAATGGCCC | 8450 |
rs770488115 | snp | A/T | 2.28802e-05 | 0.00338224 | synonymous-codon | CUL4B | GRCh38.p7 | X:120536930 | AGTAACTCTTACCTC[A/T]GGTGGTAAATGAACT | 8450 |
rs770517260 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120547578 | TTCATGCCTGTAATC[C/T]CAACATTTTGGGGGG | 8450 |
rs770619686 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120557825 | AAAATTAGAAGGGAA[C/T]CAAAAGTCTACTTAA | 8450 |
rs770657152 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120556561 | ATTGAGAGTGACGGC[G/T]GGGTTTGGTAGCTCA | 8450 |
rs770692594 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120533442 | CTTACCTAATTTTTT[A/T]ACTCACTATTCTATG | 8450 |
rs770701351 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120543538 | CACACACACACCCCT[A/T]ATAATCGAATCCTTG | 8450 |
rs770717499 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120535036 | GATTTCTGTCAAGAA[A/G]TGGCAGTGTTAGACT | 8450 |
rs770734712 | snp | A/T | 2.29766e-05 | 0.00338936 | intron-variant | CUL4B | GRCh38.p7 | X:120544446 | AAACTAGGATAGCAA[A/T]CAGCTCTGTATAGTA | 8450 |
rs770756920 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120576780 | AAATTCCAAGGGAGA[C/T]CTTGTATCTCTGGGC | 8450 |
rs770796076 | snp | G/T | 0.0026455 | 0.0362733 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120577467 | AGCTGGGTATGGTGG[G/T]GCATGTCTGTAGTCC | 8450 |
rs770813800 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120528758 | CTTGATAAATGAAGT[A/G]CCTCATAATTTAGAT | 8450 |
rs770822489 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120554246 | ACCATATAGGTAGCC[A/G]TTAGTCTCACCATCT | 8450 |
rs770860040 | snp | C/G | 3.31609e-05 | 0.00407177 | intron-variant | CUL4B | GRCh38.p7 | X:120543075 | ATTATTGACGTTTGA[C/G]TTCCAGAAAATGTAA | 8450 |
rs770952944 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120574316 | CCCGGGTTCACGCCA[G/T]TCTCCTGCCTAAGCC | 8450 |
rs770968413 | snp | A/C | 0.00112655 | 0.0237067 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120526726 | TTTATCCACTGGCTA[A/C]TGCATATGACACCAA | 8450 |
rs771003908 | in-del | -/G | 0.0174727 | 0.0918207 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CUL4B | GRCh38.p7 | X:120561442 | CCGCAGGACTTGAGT[-/G]GGGGGGGGAAGGGGG | 8450 |
rs771007831 | snp | C/T | 2.54628e-05 | 0.00356802 | intron-variant | CUL4B | GRCh38.p7 | X:120538818 | TCCAATAAAAAGTAC[C/T]GACAAAACTGCTTTA | 8450 |
rs771009821 | snp | A/G | 0.000116562 | 0.00763332 | synonymous-codon, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560386 | CCACTGAAACCCCCA[A/G]GCAGAAGGACGAGGT | 8450 |
rs771017616 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120526964 | CTCATGAATTTAATC[-/T]CCTTTTTTAAAATTT | 8450 |
rs771019451 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120563698 | TAATGCTGTGTCTTT[A/G]TAAGGGAGGATTAAC | 8450 |
rs771076668 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120571188 | TGATAGATTCCTGGA[C/T]GTTTATTTAATAATT | 8450 |
rs771092425 | in-del | -/AGC | | | intron-variant | CUL4B | GRCh38.p7 | X:120566827 | GTGAACCATCTGGAA[-/AGC]AGATTTAAGGACTAA | 8450 |
rs771109171 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120541018 | GGCTTTAGTGTAAGA[C/T]TGAAGAAAGGAAAGA | 8450 |
rs771110195 | snp | C/T | | | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120525158 | ACACCAGTGTGCAAG[C/T]TGATGCAACTAGAAA | 8450 |
rs771168516 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120572866 | TTTTCTCTTACCTTA[C/T]GTTGCTGGACTGACA | 8450 |
rs771209736 | snp | A/T | 2.4309e-05 | 0.00348625 | intron-variant | CUL4B | GRCh38.p7 | X:120540324 | TTGAGATTTTATGAC[A/T]CAAAGAACATCATTA | 8450 |
rs771214646 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120530350 | TGACATTGTTATTGC[C/T]TTAAAGGTACTGAAT | 8450 |
rs771219348 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560850 | CACCAGGAGTGAGCA[A/G]AACGAGGGGGGAGAG | 8450 |
rs771257111 | snp | A/G | 0.00844089 | 0.0644143 | intron-variant | CUL4B | GRCh38.p7 | X:120546775 | TCCTAATTTGTAAAA[A/G]AAAAAAAAAACATAG | 8450 |
rs771308556 | snp | C/T | 2.30934e-05 | 0.00339796 | intron-variant | CUL4B | GRCh38.p7 | X:120534609 | AGAAATAAAAGTGTT[C/T]AGTCATCACTTTTTT | 8450 |
rs771325534 | snp | C/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120527942 | GCAGCTACCCTTCGC[C/G]TGGTTAAATACAAAA | 8450 |
rs771328045 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120550144 | GCACCCATCATACCA[C/T]ACTGACTTAGTCATT | 8450 |
rs771361782 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120565927 | TAGAGATGAGGTTTC[A/G]CTATGTTAGCCAGGA | 8450 |
rs771382389 | snp | C/T | | | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120562933 | CAGGGGTGACAGGAT[C/T]GTGAGTGGAGTAAAA | 8450 |
rs771394607 | snp | A/G | 3.2956e-05 | 0.00405918 | synonymous-codon | CUL4B | GRCh38.p7 | X:120546598 | CTTCTTTAAAAAAAG[A/G]ACGCTATCCAATGAA | 8450 |
rs771398977 | snp | A/G | 0.00949095 | 0.0682305 | intron-variant | CUL4B | GRCh38.p7 | X:120566387 | TATATATATATATAT[A/G]TATGTATATATATTT | 8450 |
rs771506428 | snp | A/G | 2.27944e-05 | 0.00337589 | synonymous-codon | CUL4B | GRCh38.p7 | X:120534541 | CCTCATTAAACATTA[A/G]CAGCACCAGTGTTTG | 8450 |
rs771520288 | in-del | -/C | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120542053 | GGCACAACAGTAAGA[-/C]CCCCCTCCCCCTCTC | 8450 |
rs771524313 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120531189 | TAGCCGGGCATGGTC[A/G]CTCACGCATGTAGTC | 8450 |
rs771563426 | in-del | -/T | 0.0044568 | 0.0469951 | intron-variant | CUL4B | GRCh38.p7 | X:120529943 | CATATGCCAACAAAG[-/T]TTTTTTTTTTGGAAA | 8450 |
rs771596355 | snp | A/G | 0.000296648 | 0.0121752 | synonymous-codon | CUL4B | GRCh38.p7 | X:120532491 | ATCATCATTACAAAT[A/G]AACTTGTCACCATCT | 8450 |
rs771658007 | in-del | -/AG | | | intron-variant | CUL4B | GRCh38.p7 | X:120565030 | AATACAAACAAAGAC[-/AG]GGAGCTAGCTTTTAC | 8450 |
rs771686755 | in-del | -/A | 0.0346114 | 0.126916 | intron-variant | CUL4B | GRCh38.p7 | X:120543042 | TGACTTCCTACAAGG[-/A]AAAAAAAAAAGGTTA | 8450 |
rs771756172 | in-del | -/CACACACC | | | intron-variant | CUL4B | GRCh38.p7 | X:120543527 | ACACACACACACACA[-/CACACACC]CCTAATAATCGAATC | 8450 |
rs771761489 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120553162 | ATTTTAAAAAACAGC[-/A]ACAATAGTACTGATT | 8450 |
rs771767689 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120564776 | TCAAGGTTGAACTCA[C/T]GGGAGCCACACTAAT | 8450 |
rs771796486 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120553721 | ACAGCCTGGGCAACA[C/T]AGCAAGACCCCCATA | 8450 |
rs771812305 | snp | C/G | 2.32769e-05 | 0.00341144 | synonymous-codon, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560423 | GGATGCCGAATCCCT[C/G]GGTTGTAAAGGAGGA | 8450 |
rs771839500 | snp | A/C | 0.000529661 | 0.016265 | downstream-variant-500B | CUL4B | GRCh38.p7 | X:120524543 | TTAGAAGTTGTTAGG[A/C]AGATTTTAAGTCCTG | 8450 |
rs771883467 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120535004 | ACTCCCACTCTATTC[A/G]TAGCTCCCAGCAACA | 8450 |
rs771906839 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120568912 | AATAGTCTCAAGTAG[C/T]AGACATGTTAGAAAA | 8450 |
rs771924161 | in-del | -/TA | | | intron-variant | CUL4B | GRCh38.p7 | X:120556906 | TTGTACTCTGAAGTA[-/TA]TATATATTTTTTTTT | 8450 |
rs772008521 | snp | C/G | 2.77558e-05 | 0.0037252 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560677 | GAGGAGCATCAAAAA[C/G]CTACGTTTATATGCC | 8450 |
rs772028144 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120532020 | TCAGAGATTAAAATT[C/T]AGTTTCAAAGAGGTT | 8450 |
rs772046661 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120542351 | TTTCCAGGATGAAAT[A/G]ACAGTATAACTGCAT | 8450 |
rs772065058 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120568336 | AATCAAGTTTGACAG[C/T]TTATCTAAGCTGCCA | 8450 |
rs772093762 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120532656 | CTACGACATTCTACC[C/T]CAATCTAGCTTCCAC | 8450 |
rs772097422 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120566435 | GGAGTTTCGCTCTTG[G/T]TGCCCAGGCTAGAGT | 8450 |
rs772114630 | snp | C/T | 2.28167e-05 | 0.00337755 | missense | CUL4B | GRCh38.p7 | X:120541711 | TTTTCATCAAGGAGG[C/T]TATTTAAACCTGTAT | 8450 |
rs772137972 | snp | C/T | 2.27928e-05 | 0.00337578 | intron-variant | CUL4B | GRCh38.p7 | X:120534449 | TAACATAGTGGTGTG[C/T]ACATAGTGAACAATT | 8450 |
rs772156133 | snp | C/T | 6.99643e-05 | 0.00591416 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558091 | TGTCAGATACAGTAA[C/T]CAAAGATTCATAAAA | 8450 |
rs772216697 | in-del | -/G | 4.56064e-05 | 0.00477505 | intron-variant | CUL4B | GRCh38.p7 | X:120574635 | GTCCTTTGGGTCTAC[-/G]ATAGAAAACAGAGAA | 8450 |
rs772252891 | snp | C/T | 4.90118e-05 | 0.0049501 | intron-variant | CUL4B | GRCh38.p7 | X:120538230 | AAAGATGTTTGTACA[C/T]GTATAATATTTTAAA | 8450 |
rs772288046 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120541102 | GAAATTATGTCAGCC[A/G]TCAATCAGGTTTTAT | 8450 |
rs772318747 | snp | C/T | 4.78211e-05 | 0.00488961 | intron-variant | CUL4B | GRCh38.p7 | X:120538786 | CTATGTAAAAAGAAA[C/T]GCAAAATTTATAATA | 8450 |
rs772350641 | snp | G/T | 2.2791e-05 | 0.00337564 | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560149 | CAAAGCTAGAGACGG[G/T]GGTAGAAGATTTGGC | 8450 |
rs772378444 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120570783 | ATAAGTCTCAAACAA[C/T]GTTATGTGAAAAACA | 8450 |
rs772385702 | in-del | -/AAGT | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120559248 | TTACGGGTGTTGAAA[-/AAGT]AAGTCAGAAAAACAG | 8450 |
rs772401221 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120548645 | TCAAAATCAGCCTGG[A/C]CAACATAGTGAAACC | 8450 |
rs772403170 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120537568 | TCTTACTGACCCTGA[C/T]TTTTTCTTAATTCTT | 8450 |
rs772427745 | snp | A/C | | | downstream-variant-500B | CUL4B | GRCh38.p7 | X:120524587 | TTCTTACAATACTTG[A/C]ATTTTAAAGATCTTC | 8450 |
rs772521398 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120527461 | ATGTCGCCCAGGCTG[A/G]CCTTAAACTCTTGTT | 8450 |
rs772538051 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561889 | TTTTAATTCGGTGCC[A/G]GTATAAATTGTTTCT | 8450 |
rs772539641 | snp | C/T | 1.7894e-05 | 0.0029911 | intron-variant | CUL4B | GRCh38.p7 | X:120545413 | GAGTATGATTTGGAA[C/T]AATCTTTTCATATTT | 8450 |
rs772560676 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120542511 | GTGCTTGGTTTGACA[C/T]GCCATGAACAACAAA | 8450 |
rs772594153 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120533178 | AACATAATAGCTAGC[C/T]GCTGCTTCCGCAGAG | 8450 |
rs772597680 | in-del | -/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120531330 | ACCTCAAAAAAAAAA[-/T]TTTTTTTTTTTTCAA | 8450 |
rs772626145 | in-del | -/ACA | 0.00896606 | 0.0663524 | intron-variant | CUL4B | GRCh38.p7 | X:120570066 | AATCTCAAGTCTGGT[-/ACA]GCAATCTTAGGCCTC | 8450 |
rs772638429 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120536234 | CCTTTATTTCACTGT[A/T]GCTTCTGCATTGGTT | 8450 |
rs772669717 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120567163 | GAGTTTGGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 8450 |
rs772726129 | snp | A/G | | | utr-variant-5-prime | CUL4B | GRCh38.p7 | X:120575799 | TAAACTGAACTGCTG[A/G]GGAGGGATTGTGTCT | 8450 |
rs772905667 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120535367 | AAAGCTATGACAAAC[G/T]ATCACTGTCATCATG | 8450 |
rs772926238 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120546041 | ATCAAGAGAGAAAAA[A/T]AAATAAGAGTGACAG | 8450 |
rs772933670 | snp | A/C | 2.32337e-05 | 0.00340827 | synonymous-codon | CUL4B | GRCh38.p7 | X:120540482 | ATCAATTATATGGTC[A/C]ACCTTATCTTTAAAA | 8450 |
rs772935571 | snp | A/C | 2.80489e-05 | 0.00374482 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560681 | AGCATCAAAAACCTA[A/C]GTTTATATGCCTGCG | 8450 |
rs772943399 | snp | C/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120556426 | TACCATCTTATATTT[C/G]TAAGATTATAGTGCC | 8450 |
rs773023455 | snp | A/G | 4.64679e-05 | 0.00481993 | synonymous-codon, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560438 | GGGTTGTAAAGGAGG[A/G]GTGGAAGAGGAGGAA | 8450 |
rs773104825 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120532753 | CCAATGGCTTTTTTC[A/C]TAGTCCTCTTCTTTT | 8450 |
rs773131729 | snp | G/T | 2.28295e-05 | 0.00337849 | missense | CUL4B | GRCh38.p7 | X:120541714 | TCATCAAGGAGGTTA[G/T]TTAAACCTGTATTTT | 8450 |
rs773217823 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120528034 | GTTTTGTCAAGATAG[C/T]TCATGAAGCACACCT | 8450 |
rs773304179 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120527303 | CCTCAGGTGATCCAC[A/C]TGCCTCAGCCTCCCA | 8450 |
rs773335186 | snp | C/T | 2.4478e-05 | 0.00349834 | intron-variant | CUL4B | GRCh38.p7 | X:120538800 | ATGCAAAATTTATAA[C/T]ATTCCAATAAAAAGT | 8450 |
rs773356422 | in-del | -/A | 0.000529661 | 0.016265 | downstream-variant-500B | CUL4B | GRCh38.p7 | X:120524454 | CTCCCCCATACTCTT[-/A]ATAGCATTACCACAA | 8450 |
rs773371743 | in-del | -/CTT | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120559496 | TACACAGAGTTACTA[-/CTT]CTGTGTATACACAAT | 8450 |
rs773389833 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120538493 | AAAAAAAACAACTCT[A/G]GATATTATGTACAAT | 8450 |
rs773389984 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120549408 | AATACAAAAATTAGC[C/T]GGGTGTGGTGGTGTG | 8450 |
rs773406492 | snp | A/G | | | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120524685 | GAGCACAAAAATTCA[A/G]CTGATACAGAACAAC | 8450 |
rs773458162 | snp | A/G | 0.00370565 | 0.0428847 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560782 | CGAGAAGGAAAGTGA[A/G]GGGGGGGGCTACACC | 8450 |
rs773473505 | snp | A/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120568384 | AATTTAAATATTTTT[A/T]ATAAGCAAAGCAGAG | 8450 |
rs773478629 | snp | C/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120546295 | TACTGCTCTGGTGAA[C/G]GGTGCACCAAAATCT | 8450 |
rs773518260 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120556110 | CTTAAGGCCTTTCCA[A/G]GTCAGTTTCATATTT | 8450 |
rs773518934 | snp | A/G | 2.27905e-05 | 0.00337561 | synonymous-codon | CUL4B | GRCh38.p7 | X:120574576 | AGAGGTAGTAGCCTC[A/G]TCATCATTCCCATCT | 8450 |
rs773549112 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120548711 | TGGTGGTGCACGCCT[A/G]TAATCCCAGCTACTC | 8450 |
rs773563529 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120570939 | GTATGCACCTGTAGT[A/C]CCAGCTACTTGGGAG | 8450 |
rs773590497 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | CUL4B | GRCh38.p7 | X:120530533 | GTAGAGATAGCTGAT[A/G]TGGAATTTACCATTT | 8450 |
rs773655024 | snp | A/G | 2.27985e-05 | 0.0033762 | missense | CUL4B | GRCh38.p7 | X:120532534 | CCCTTTGGATTTTTC[A/G]CCAGAACTCTAGCTT | 8450 |
rs773673177 | snp | A/C/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120531108 | ATGGGCGGATCATGA[A/C/G]GTCAGGAGTTCAAGA | 8450 |
rs773677360 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120565870 | AGCTGGGACTACAGG[C/T]GCCTACCACCACGCC | 8450 |
rs773740692 | snp | C/T | 2.37852e-05 | 0.00344848 | intron-variant | CUL4B | GRCh38.p7 | X:120526893 | CAATGTAAAGTTCAT[C/T]ATCATTGGCTCAAGC | 8450 |
rs773763649 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120565081 | CTGTGGACATCTCCC[G/T]AAAAAGGCAGAGTGT | 8450 |
rs773773171 | snp | A/T | | | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560349 | CGCAGCTTCTTCTGT[A/T]TCGGTACGTGGCTGG | 8450 |
rs773782697 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120528198 | GATCACCTGAGGTCA[A/G]AAGTTTGAGACCAGA | 8450 |
rs773801923 | snp | A/T | 9.44153e-05 | 0.00687013 | intron-variant | CUL4B | GRCh38.p7 | X:120545416 | TATGATTTGGAACAA[A/T]CTTTTCATATTTTTC | 8450 |
rs773815482 | in-del | -/ACACACACA | | | intron-variant | CUL4B | GRCh38.p7 | X:120543524 | CACACACACACACAC[-/ACACACACA]CCCCTAATAATCGAA | 8450 |
rs773866810 | in-del | -/G | 0.00633741 | 0.0559334 | intron-variant | CUL4B | GRCh38.p7 | X:120537506 | AAAAAGAGGGGAAAA[-/G]GGCAAAGCAGATAAG | 8450 |
rs773872299 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120539654 | ATACGGATATCCTGT[C/G]GGGGAGGTCTCATGT | 8450 |
rs773945781 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120537641 | GTCACTACTAAAACC[C/T]AAAAGAGGAAAATCT | 8450 |
rs773945968 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120563706 | TGTCTTTATAAGGGA[G/T]GATTAACTGACTCAT | 8450 |
rs773956388 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120568062 | CCTCCTTCTCTAGGA[A/G]TCCTTTTTTAAAGTG | 8450 |
rs774020573 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120573691 | ACAAAAACAAAGTAA[A/G]AGCAGGAGTGCTCTC | 8450 |
rs774112895 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120539807 | ACATCGTAGAGTAGA[A/C]GGTAAAATTTGCTAC | 8450 |
rs774113038 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120563148 | GGCTCTAATGGAACT[C/T]AGAACCGCTGAGAAG | 8450 |
rs774161698 | snp | C/T | 0.00370173 | 0.0428621 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120577559 | GAGCAGAGATCACGC[C/T]ACTGTACTCTAACCT | 8450 |
rs774172669 | snp | C/T | 5.02046e-05 | 0.00500997 | missense | CUL4B | GRCh38.p7 | X:120539286 | AGATAAATCTAAATA[C/T]GATCATAATTTTATC | 8450 |
rs774247754 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120550953 | ATCTCTGGAAAGATA[C/T]CCAAAAAACTAATAA | 8450 |
rs774268469 | snp | C/G | 2.28277e-05 | 0.00337836 | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560287 | AGGAGGAGGATTCCT[C/G]AGCCATCTTCGCATC | 8450 |
rs774317062 | snp | A/C | 0.000529661 | 0.016265 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120576781 | AATTCCAAGGGAGAT[A/C]TTGTATCTCTGGGCC | 8450 |
rs774354111 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120553087 | ACATTTTAAAATTTT[C/T]TATTATTTAATAATC | 8450 |
rs774363065 | snp | A/G | 2.68868e-05 | 0.00366642 | intron-variant | CUL4B | GRCh38.p7 | X:120547097 | AGGGACAGAGAGGAA[A/G]ACAAAACTATTCACG | 8450 |
rs774462583 | in-del | -/G | 0.0174727 | 0.0918207 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CUL4B | GRCh38.p7 | X:120561441 | CCGCAGGACTTGAGT[-/G]GGGGGGGGGAAGGGG | 8450 |
rs774463977 | snp | C/T | 0.00422943 | 0.0457911 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120526082 | CTTGGGGCTAAGCCA[C/T]ATACACACATCCCAT | 8450 |
rs774468783 | snp | C/T | 0.000185522 | 0.00962946 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120557888 | TCCCACCTCAATTTA[C/T]GTTAATCAAATCTGG | 8450 |
rs774470033 | snp | A/T | 3.24186e-05 | 0.00402595 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558083 | GAATACCATGTCAGA[A/T]ACAGTAACCAAAGAT | 8450 |
rs774608326 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120541066 | CTTTTTCTACATTTA[C/T]TGCTTTAAGTGGTAG | 8450 |
rs774615455 | in-del | -/G | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120550460 | GATAAGCAGAGAGAT[-/G]AGGCCCCTAACCCAG | 8450 |
rs774645450 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120546203 | CTCAACCAAAACTAG[C/T]TTCCAATTCAGAAAA | 8450 |
rs774655606 | snp | A/T | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120546776 | CCTAATTTGTAAAAG[A/T]AAAAAAAAACATAGT | 8450 |
rs774746965 | snp | C/T | 4.56293e-05 | 0.00477625 | synonymous-codon | CUL4B | GRCh38.p7 | X:120536963 | CATAGGCACATATGT[C/T]GGCCAATAGCCCATT | 8450 |
rs774775981 | snp | A/T | 2.30097e-05 | 0.0033918 | intron-variant | CUL4B | GRCh38.p7 | X:120544432 | TGTGGGGGGAAAAAA[A/T]ACTAGGATAGCAATC | 8450 |
rs774781959 | in-del | -/A | | | intron-variant | CUL4B | GRCh38.p7 | X:120556912 | CTGAAGTATATATAT[-/A]ATTTTTTTTTTTTTT | 8450 |
rs774791368 | in-del | -/T | 0.00211696 | 0.0324653 | intron-variant | CUL4B | GRCh38.p7 | X:120566390 | ATATATATATATATA[-/T]GTATATATATTTGGG | 8450 |
rs774840403 | snp | C/T | 2.38646e-05 | 0.00345424 | intron-variant | CUL4B | GRCh38.p7 | X:120543690 | CAAGTGATTTAACGA[C/T]AGTTTAAGACTATTA | 8450 |
rs774860011 | snp | A/G | 2.28457e-05 | 0.00337969 | missense | CUL4B | GRCh38.p7 | X:120543751 | TGATCTAAGTAAGTA[A/G]TAAGTCTGTCTGCTT | 8450 |
rs774862000 | snp | A/G | 2.27925e-05 | 0.00337576 | missense | CUL4B | GRCh38.p7 | X:120574562 | TCACCACCGTCTTTA[A/G]AGGTAGTAGCCTCAT | 8450 |
rs774892768 | snp | C/T | | | downstream-variant-500B | CUL4B | GRCh38.p7 | X:120524114 | ACACAGCAAAAATTT[C/T]AAGAGTATGGCTAGA | 8450 |
rs774909127 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120556223 | TAGCTTAGTACTACA[A/G]CTACTAGCCGACATT | 8450 |
rs774912958 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120577821 | TAGACTTTACCTTCC[A/G]TGAAACTAGGAGTGG | 8450 |
rs774927155 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120531961 | TCCTAAAATGTTCAT[A/G]CCCTTTAACCCAAAA | 8450 |
rs774985544 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120564941 | ACTTTACAATGTTGC[C/G]ACATGAAGTGTAGTT | 8450 |
rs775020740 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120531195 | GGCATGGTCGCTCAC[A/G]CATGTAGTCCCAGCT | 8450 |
rs775102321 | snp | A/C | 0.00105904 | 0.0229869 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560921 | CTCCCCTGCTTTTCG[A/C]TCTCTCTCCCCCCCT | 8450 |
rs775146882 | snp | C/T | 4.56387e-05 | 0.00477674 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120526760 | CTGCAAGGCCAACAT[C/T]CTATGCAATATAGTT | 8450 |
rs775186476 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558352 | TCCTGATCTTATTTC[A/G]TCATGTGTAAAACCT | 8450 |
rs775282175 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120563999 | TTCTGAGTTACATGT[C/T]GGTTTTAAAAAGCAC | 8450 |
rs775321115 | snp | C/T | 2.28198e-05 | 0.00337778 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560035 | GAGCACGTGACCCCT[C/T]GAGTGTCAAATCCTT | 8450 |
rs775334942 | snp | C/T | 5.11673e-05 | 0.00505777 | intron-variant | CUL4B | GRCh38.p7 | X:120538821 | AATAAAAAGTACTGA[C/T]AAAACTGCTTTAAAG | 8450 |
rs775397648 | in-del | -/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120556621 | AGGTGACAAGACTGC[-/T]TGTAGCCCTGGAGTT | 8450 |
rs775488694 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120534366 | TCTCATTAAAAAAAA[A/G]GAAAAAAAAAACTCA | 8450 |
rs775568620 | snp | A/T | 0.00844089 | 0.0644143 | intron-variant | CUL4B | GRCh38.p7 | X:120531330 | CACCTCAAAAAAAAA[A/T]TTTTTTTTTTTTCAA | 8450 |
rs775587170 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120541188 | TACTTTTTAAACAAA[C/T]TTAAAATTCCCTTAA | 8450 |
rs775588616 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120552852 | TAGTAAGTAAAGCAC[A/G]TAACAAAAAATTCAA | 8450 |
rs775588619 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120557056 | AGCTGGGATTACAGG[A/C]ATGCACCACATTGCC | 8450 |
rs775663269 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120567174 | TGTCGCCCAGGCTGG[A/G]GTGCAGTGGTGCAAT | 8450 |
rs775768820 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | CUL4B | GRCh38.p7 | X:120542409 | ACAAAAGAAAATATT[A/G]TTGGGGAGAAAGGTA | 8450 |
rs775784267 | snp | A/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120540969 | TCCTTATTTTTAAAG[A/T]AGTCAGCTTTCAACT | 8450 |
rs775787797 | snp | C/T | 2.28045e-05 | 0.00337664 | intron-variant | CUL4B | GRCh38.p7 | X:120535791 | CCTAAACATTAAAGA[C/T]AAAGATGAAAACTAA | 8450 |
rs775787840 | snp | A/C | 4.72361e-05 | 0.00485961 | missense | CUL4B | GRCh38.p7 | X:120547210 | GTACAAGTTTGCAGA[A/C]ATCTTGTAAGAACAG | 8450 |
rs775828611 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120576465 | TGGCTTGTATTAGGA[C/T]TCTTGTTTGCAAGTG | 8450 |
rs775872231 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120537613 | CACCTTAGCAACACT[C/G]TGGGGTAAAGAAGTC | 8450 |
rs775875743 | snp | A/G | 3.09129e-05 | 0.00393134 | intron-variant | CUL4B | GRCh38.p7 | X:120546654 | TTTAAAGCGTTTGGT[A/G]CAAGTCATATGTGCC | 8450 |
rs775945971 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120542724 | AGCTGATACTACAGG[C/T]ACATATCAACCACTG | 8450 |
rs775982228 | snp | A/G | 2.28634e-05 | 0.003381 | missense | CUL4B | GRCh38.p7 | X:120536934 | ACTCTTACCTCTGGT[A/G]GTAAATGAACTTCCA | 8450 |
rs775985918 | snp | C/T | 3.4756e-05 | 0.00416855 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561327 | GGGAACTCCCACTCC[C/T]TCCTTAACGGTCCCG | 8450 |
rs776144989 | snp | C/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120556640 | AGCCCTGGAGTTCAA[C/G]ACCAGCCTGGGCAAC | 8450 |
rs776242480 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120545913 | GATTTTAATCTGTAG[A/G]ATATAAGGTATAAAC | 8450 |
rs776364726 | snp | C/T | 2.61671e-05 | 0.00361702 | synonymous-codon, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558023 | ATCTGTGTAGTTTTC[C/T]GGTAATTTAGGCTTA | 8450 |
rs776408805 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120545093 | GGGAAGAGTTCATGA[C/T]ACTATTCTATTTTCG | 8450 |
rs776441778 | snp | C/G | 2.29933e-05 | 0.00339059 | intron-variant | CUL4B | GRCh38.p7 | X:120541768 | AGTGAACAAAAAAGT[C/G]AACAAGATTATCAGA | 8450 |
rs776507092 | in-del | -/TCCCCA | 2.47669e-05 | 0.00351892 | intron-variant | CUL4B | GRCh38.p7 | X:120543843 | ACATTATTGTTTTCC[-/TCCCCA]TAAATCATTCAGAAA | 8450 |
rs776528029 | snp | G/T | 0.0026455 | 0.0362733 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561608 | GGGGAGGGAAGGTAG[G/T]GACGGCGAGGGGCGG | 8450 |
rs776618088 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561002 | TTCTCCCTCTCCCTG[A/G]GAGGGGAGAGGCTGT | 8450 |
rs776630950 | snp | A/T | 0.0026455 | 0.0362733 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120526185 | CTTGTTTCCAAATAA[A/T]TTTTTTTAAAAAACA | 8450 |
rs776654164 | in-del | -/TATTTT | | | intron-variant | CUL4B | GRCh38.p7 | X:120556912 | TCTGAAGTATATATA[-/TATTTT]TTTTTTTTTTTGAGA | 8450 |
rs776698914 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120569772 | CCTGGCCCAGCCTAG[G/T]AGGGTGAGGTGGGGT | 8450 |
rs776708896 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120536106 | TCTCCCAACCACCAA[A/G]TCAAATGGGATTTAT | 8450 |
rs776716913 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120571420 | TAGGATTGATTTTTG[C/T]AACATTTAAGCATAC | 8450 |
rs776725529 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120547934 | TTCTTCAGTTTTGGG[A/G]ATCAACCTGGCTCTC | 8450 |
rs776735002 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120532214 | ATAAACAAAGTAAGA[C/T]ATGAAACTATGTTGA | 8450 |
rs776777559 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120527945 | GCTACCCTTCGCGTG[A/G]TTAAATACAAAAGAC | 8450 |
rs776778280 | in-del | -/A | | | intron-variant | CUL4B | GRCh38.p7 | X:120565395 | AACAAAACAAAACAG[-/A]AAAAACGGCTGGGCA | 8450 |
rs776830204 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120533397 | CATTTGCTAGACTTA[C/T]CAGGTTCTCCACAAT | 8450 |
rs776835850 | snp | C/T | 4.56997e-05 | 0.00477993 | synonymous-codon | CUL4B | GRCh38.p7 | X:120532581 | CTGCAGTGTTCTCCT[C/T]AACTCTCCATCCTCT | 8450 |
rs776907324 | snp | A/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560705 | GCCTGCGTGCGTGTA[A/G]GAGAGAAGGTAGCAA | 8450 |
rs776907411 | in-del | -/GAG | | | cds-indel, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560268 | GGTGAAGATGAGGAG[-/GAG]GAGGAGGAGGATTCC | 8450 |
rs776960557 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120567980 | GAATGGGGCTGATAA[C/G]CACTTGTATTCCGTT | 8450 |
rs776962581 | snp | C/T | 2.86936e-05 | 0.00378761 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558050 | CTTATCTAGATGATA[C/T]GTAAAAGGTTGGCAT | 8450 |
rs776966744 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120550146 | ACCCATCATACCACA[C/T]TGACTTAGTCATTGA | 8450 |
rs776991033 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120538416 | CCTTATCTACTATTT[A/T]GGTATAAAATAAATG | 8450 |
rs777009193 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120548685 | CTAAAAATACAAAAA[G/T]TAGCCGGACATGGTG | 8450 |
rs777094163 | in-del | -/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120539589 | AAACCCAAGTGTTCT[-/G]ACTCCAGATCAAATG | 8450 |
rs777192354 | snp | G/T | | | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120563008 | CAAATAAATCAACTT[G/T]CTAACTTTGTTTAAA | 8450 |
rs777222761 | snp | A/T | 1.64765e-05 | 0.00287019 | intron-variant | CUL4B | GRCh38.p7 | X:120534615 | AAAAGTGTTTAGTCA[A/T]CACTTTTTTAAAAAC | 8450 |
rs777238263 | in-del | -/TACTGCTGC | 4.83723e-05 | 0.0049177 | cds-indel, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560491 | TCTCGTTACTACTGT[-/TACTGCTGC]TACTGCTGCTGCTGT | 8450 |
rs777321886 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120531844 | AGAAAATATAATCTT[C/T]AGTGCTGGGGGACAT | 8450 |
rs777352807 | snp | A/C | 2.39444e-05 | 0.00346 | intron-variant | CUL4B | GRCh38.p7 | X:120537085 | AACTGCATACATTTC[A/C]TATCATAATAACCTA | 8450 |
rs777387009 | snp | A/G/T | 0.00105904 | 0.0229869 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120557607 | TATCACAATAGAATG[A/G/T]CATGTCACCAGAAAT | 8450 |
rs777425786 | in-del | -/G | 4.61537e-05 | 0.00480361 | intron-variant | CUL4B | GRCh38.p7 | X:120532645 | AGCATGAACAACTAC[-/G]ACATTCTACCTCAAT | 8450 |
rs777463277 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120545381 | CTTATACACTTTCAT[C/T]AGTGTAATTAAGATT | 8450 |
rs777589489 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120548330 | ACAAGCAGAGCTTCA[C/T]TTTGGGTTTAAAAAA | 8450 |
rs777593670 | in-del | -/A | 0.0346114 | 0.126916 | intron-variant | CUL4B | GRCh38.p7 | X:120543041 | TGACTTCCTACAAGG[-/A]AAAAAAAAAAAGGTT | 8450 |
rs777670956 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561342 | CTCCTTAACGGTCCC[A/G]CGGGAAGCTTCGCGC | 8450 |
rs777680065 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120529910 | TCTGTTATTTTTCCC[C/T]TTTGTCACTGCTGCC | 8450 |
rs777700759 | snp | C/T | 0.00020567 | 0.0101387 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CUL4B | GRCh38.p7 | X:120561418 | GCCCAGATCCCGAAG[C/T]CCCCAGGTCCGCAGG | 8450 |
rs777746297 | snp | A/G | | | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120559383 | TCTCAAACACGGTCT[A/G]AACAAATTTTCCTAA | 8450 |
rs777750094 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120534717 | TATCCAGCAAAGCCA[C/T]TTGACGTGGTAATAC | 8450 |
rs777767894 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120528672 | GCTGCAGTGAGCCAA[C/G]ATCATGCCACTGCAC | 8450 |
rs777789781 | in-del | -/A | 0.000530223 | 0.0162736 | intron-variant | CUL4B | GRCh38.p7 | X:120546409 | AATTTTTAAAAAAAG[-/A]AAAAAAAAGAAAAGG | 8450 |
rs777791888 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120537451 | AGTTTTTCACTTGCT[C/T]CACTGCCTGTCTGCA | 8450 |
rs777792521 | snp | G/T | 0.000113792 | 0.00754207 | intron-variant | CUL4B | GRCh38.p7 | X:120544072 | AAAGTAAGGTCTATT[G/T]TGAGAGACAGTGAGA | 8450 |
rs777805257 | snp | C/T | 2.27936e-05 | 0.00337584 | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560207 | CACAGAAGAGATTAA[C/T]ATACTCTTATTTTTA | 8450 |
rs777827345 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120572510 | GAAATGTCCAGGTCT[C/T]AACAACCTTTGACTA | 8450 |
rs777832630 | snp | C/T | 0.0152462 | 0.0859689 | intron-variant | CUL4B | GRCh38.p7 | X:120569509 | GGGACTACAGGCGCC[C/T]GCCACCACGCCCGGC | 8450 |
rs777885049 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | CUL4B | GRCh38.p7 | X:120535556 | AAAAATACAAAAAAA[A/G]TTAGCTGGGTATGGT | 8450 |
rs777886723 | snp | C/T | 0.00317376 | 0.039709 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120525995 | CTCTTCTATGATGTT[C/T]CTCTAGTACAACTGA | 8450 |
rs777900826 | snp | C/T | 3.24112e-05 | 0.00402549 | intron-variant | CUL4B | GRCh38.p7 | X:120543068 | GGTTAGTATTATTGA[C/T]GTTTGACTTCCAGAA | 8450 |
rs777919576 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120571554 | CCTGTATATTAATCA[C/T]ACAAATCCAAACTTA | 8450 |
rs777992293 | snp | G/T | 5.9917e-05 | 0.00547311 | intron-variant | CUL4B | GRCh38.p7 | X:120540601 | TTACTGTAATCGAAT[G/T]GTCTACAATGAAAAC | 8450 |
rs777998150 | snp | C/G | 0.000400075 | 0.0141378 | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560367 | GGTACGTGGCTGGAA[C/G]CAGCCACTGAAACCC | 8450 |
rs778059992 | in-del | -/TATATATATATATAT | 0.00317712 | 0.0397299 | intron-variant | CUL4B | GRCh38.p7 | X:120566376 | ATATATATATATATA[-/TATATATATATATAT]GTATATATATTTGGG | 8450 |
rs778087213 | snp | A/G | 2.57003e-05 | 0.00358462 | missense | CUL4B | GRCh38.p7 | X:120546593 | TCAATCTTCTTTAAA[A/G]AAAGAACGCTATCCA | 8450 |
rs778122011 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120568890 | TTCGTAAGGAGACTT[A/G]CCATAAAATAGTCTC | 8450 |
rs778155525 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120572551 | TGAAATCTCCACTCA[G/T]TCCCTGTTCCCCAAC | 8450 |
rs778161232 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120549917 | ACTTAGTGCGTACTT[C/T]ATCTTTCCACATTGT | 8450 |
rs778201156 | in-del | -/TT | | | intron-variant | CUL4B | GRCh38.p7 | X:120552072 | TTTACATATTATGCA[-/TT]GTTTTATTTAAATAT | 8450 |
rs778215551 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120529428 | AAGTGATTTATGAAA[A/G]TCCAAAGCTCATAAG | 8450 |
rs778235943 | snp | A/G | | | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120562722 | CGGAAACAAGGGCAA[A/G]GCAAGGAGTGAAAGG | 8450 |
rs778254097 | in-del | -/GT | | | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120562803 | GATGTCTGGCTGGGA[-/GT]AAGGAAGATGAGGCT | 8450 |
rs778260689 | in-del | -/TCT | | | intron-variant | CUL4B | GRCh38.p7 | X:120563982 | ATCTAAGCCCTTCAG[-/TCT]TCTGAGTTACATGTT | 8450 |
rs778293185 | in-del | -/TATG | 1.6486e-05 | 0.00287102 | intron-variant | CUL4B | GRCh38.p7 | X:120538779 | CCTTGCCTATGTAAA[-/TATG]AAGAAATGCAAAATT | 8450 |
rs778308198 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120574880 | GGAAAACACATTTGT[A/T]AAGATTCTCTTAAAT | 8450 |
rs778324352 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120527718 | TTTTGACTGCAACCT[A/G]TCAAATGAGGTAAAG | 8450 |
rs778328941 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120541954 | TAAAAACAGGCCAGG[A/C]ACGGTGGCTCACACC | 8450 |
rs778382925 | snp | C/G | 2.38212e-05 | 0.00345109 | intron-variant | CUL4B | GRCh38.p7 | X:120544659 | CTAAAATAAAAAACA[C/G]ATATAACCTAAATTA | 8450 |
rs778401536 | in-del | -/A | | | intron-variant | CUL4B | GRCh38.p7 | X:120567718 | ACCCTGTCTCTATCG[-/A]AAAAAAAAAAAAAAA | 8450 |
rs778416837 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120551287 | CAGTGCAACCTCTGC[C/G]TCCAGGTTCCAGTGG | 8450 |
rs778479810 | in-del | -/C | 4.6151e-05 | 0.00480347 | frameshift-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560336 | GGTGTCTTCAAAACG[-/C]AGCTTCTTCTGTATC | 8450 |
rs778493021 | snp | C/T | 2.27928e-05 | 0.00337578 | intron-variant | CUL4B | GRCh38.p7 | X:120534456 | GTGGTGTGCACATAG[C/T]GAACAATTAATGTTT | 8450 |
rs778529908 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120548509 | AGGAATTTTCTCCAA[C/T]ATTTCAGTTTAAGAA | 8450 |
rs778544466 | in-del | -/ACACACC | | | intron-variant | CUL4B | GRCh38.p7 | X:120543528 | CACACACACACACAC[-/ACACACC]CCTAATAATCGAATC | 8450 |
rs778579288 | snp | C/T | 5.03404e-05 | 0.00501674 | synonymous-codon | CUL4B | GRCh38.p7 | X:120546574 | ATGGTTTTGCCAGCA[C/T]CTATCAATCTTCTTT | 8450 |
rs778698343 | in-del | -/A | 0.00211696 | 0.0324653 | intron-variant | CUL4B | GRCh38.p7 | X:120554400 | CAGTCAATTAAAAAC[-/A]AGCACGCAAACAAAC | 8450 |
rs778742058 | snp | C/T | 0.00158814 | 0.0281345 | | | GRCh38.p7 | X:120533958 | GTAATCCCAGCTACT[C/T]GGGAGGCAGAGGCAG | 8450 |
rs778785061 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120545010 | TGGTTATTTATCAAC[G/T]GGTTTCAATACTGAA | 8450 |
rs778805165 | in-del | -/AATTT | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120555460 | TCCCTAAAGTAAAAC[-/AATTT]AATTGTTTCAAACAC | 8450 |
rs778828543 | in-del | -/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120572553 | AAATCTCCACTCAGT[-/C]CCTGTTCCCCAACTA | 8450 |
rs778898457 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120551477 | AAGTGCTGGATTACA[C/T]GCATGAGCCACCTTG | 8450 |
rs778922364 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120557417 | CTGGACTACAAACTG[C/T]TACTCATTTCTGGGC | 8450 |
rs778937697 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120528867 | TAGCTTTATCTTCAT[A/G]ATTGCATTCTAAGCT | 8450 |
rs778938313 | snp | A/G | 3.30655e-05 | 0.00406591 | upstream-variant-2KB, missense, intron-variant | CUL4B | GRCh38.p7 | X:120561398 | GGGCAGACACTTTTC[A/G]TAGCGCCCAGATCCC | 8450 |
rs779001806 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120573705 | AAAGCAGGAGTGCTC[C/T]CTTGACCACCATCCC | 8450 |
rs779001856 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120564605 | AGAAAGAGTCTGTCT[A/C]AAAAAAAAACAAAAA | 8450 |
rs779095996 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120562594 | GGCAAAACAAGAAAT[C/T]TGGGAGAAATCTGGA | 8450 |
rs779112530 | in-del | -/A | 0.00633741 | 0.0559334 | intron-variant | CUL4B | GRCh38.p7 | X:120570530 | CTAGTTCCTTAACAG[-/A]AAAAAAAAATTGCCA | 8450 |
rs779135099 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120526978 | CTCCTTTTTTAAAAT[G/T]TTTATTTATTTAAAT | 8450 |
rs779141130 | snp | A/G | 9.11567e-05 | 0.00675056 | synonymous-codon, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560132 | GCCAGGTTTGCTGTT[A/G]GCAAAGCTAGAGACG | 8450 |
rs779144333 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560348 | ACGCAGCTTCTTCTG[C/T]ATCGGTACGTGGCTG | 8450 |
rs779211402 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120557682 | TCTATTACACCAAGG[C/T]ACACGTAACTGTAAT | 8450 |
rs779224877 | snp | A/T | 0.0152462 | 0.0859689 | intron-variant | CUL4B | GRCh38.p7 | X:120535703 | GAGTGAGACTCTGTC[A/T]CAAAAAAAAAAAAAA | 8450 |
rs779263929 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120536566 | CCTGGGAAGATGGAA[G/T]AAGAGCCAGGGAAAT | 8450 |
rs779309919 | in-del | -/A | 0.00475684 | 0.0485365 | intron-variant | CUL4B | GRCh38.p7 | X:120542088 | TTAATTCAAAAAGTT[-/A]AAAAAATTAAAAAGA | 8450 |
rs779335268 | snp | A/T | 1.64822e-05 | 0.00287068 | intron-variant | CUL4B | GRCh38.p7 | X:120538778 | ATCCTTGCCTATGTA[A/T]AAAGAAATGCAAAAT | 8450 |
rs779340604 | snp | C/T | 4.8901e-05 | 0.0049445 | intron-variant | CUL4B | GRCh38.p7 | X:120539405 | TTTGTTGTTTAATAA[C/T]CGGGGAATACACGAG | 8450 |
rs779346425 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120549854 | CGTTCCTTCTGAATG[A/G]CTGTTTTCTCAGCAT | 8450 |
rs779362244 | snp | C/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120548293 | TAAAAAAGCTGTCTT[C/G]TTTAAAATGTTAATC | 8450 |
rs779408840 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | CUL4B | GRCh38.p7 | X:120543109 | CTCTCCTGAGGGGGG[A/G]AAAAAATCAAATAGC | 8450 |
rs779455069 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120567032 | ACTTTATCGATGTCT[C/T]TCAAAGTCCCTCCAA | 8450 |
rs779474890 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120533075 | ATATAACTGTGTCCT[C/G]TTTCCAATTGTCAGT | 8450 |
rs779514451 | snp | C/T | 2.31166e-05 | 0.00339967 | synonymous-codon | CUL4B | GRCh38.p7 | X:120544619 | ACTTATAATATGAGC[C/T]CTAAATAACTCCAGT | 8450 |
rs779515448 | snp | C/T | 2.27957e-05 | 0.00337599 | intron-variant | CUL4B | GRCh38.p7 | X:120574548 | ACTAGTTCATTTACT[C/T]ACCACCGTCTTTAGA | 8450 |
rs779540403 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120577154 | TTTCTCTTTCTTTTA[A/G]ATTTATACAGCTTAT | 8450 |
rs779579405 | snp | C/T | 0.01368 | 0.0815649 | intron-variant | CUL4B | GRCh38.p7 | X:120565783 | CAGGCTGGAGTGCAG[C/T]GGCGCCATCTCAGCT | 8450 |
rs779586437 | in-del | -/T | 0.00317376 | 0.039709 | intron-variant | CUL4B | GRCh38.p7 | X:120549098 | GTAATGACTTAAATG[-/T]TAACACCAGAATTCC | 8450 |
rs779643118 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120572830 | AAAAAATCTAATTAT[C/T]ACACGTTATTGTTGT | 8450 |
rs779672829 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120539550 | TTCAGTGCCATAGAG[C/T]TAATAACATCAGGGC | 8450 |
rs779779626 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120569571 | TTCACCGTGTTAGCC[A/G]GGATGGTCTCGATCT | 8450 |
rs779806461 | in-del | -/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120565212 | TAGGTCCTCTCCAGA[-/T]TATCTCATACCAGTG | 8450 |
rs779869075 | in-del | -/TG | 0.0525795 | 0.153379 | intron-variant | CUL4B | GRCh38.p7 | X:120566365 | ATATATATATATATA[-/TG]TATATATATATATAT | 8450 |
rs779894905 | snp | A/G | 2.82247e-05 | 0.00375653 | intron-variant | CUL4B | GRCh38.p7 | X:120546517 | ATTAATACAATGTTT[A/G]GCCGAAATACAATAC | 8450 |
rs779953823 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120563557 | AGTAAACTCTTAAGG[A/C]CAGGAAAGACACCTT | 8450 |
rs779974420 | snp | A/G | 2.33184e-05 | 0.00341448 | synonymous-codon, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560387 | CACTGAAACCCCCAG[A/G]CAGAAGGACGAGGTT | 8450 |
rs779993669 | snp | A/T | 2.60342e-05 | 0.00360783 | intron-variant | CUL4B | GRCh38.p7 | X:120543036 | AATTAATGACTTCCT[A/T]CAAGGAAAAAAAAAA | 8450 |
rs780015369 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | CUL4B | GRCh38.p7 | X:120541640 | GCAAAAGAACCTGAA[C/T]TCCACCTCGAACTCT | 8450 |
rs780104726 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120555518 | ACCAGGGTATATTAG[G/T]GAGGTGGTACAGGAG | 8450 |
rs780135909 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120545798 | ACGCTCATATAATTC[G/T]TCCTGCGCCACAGTG | 8450 |
rs780148984 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120553934 | TTTTTAAGCGTAGAG[A/G]GACACTGTTCCTAGA | 8450 |
rs780152474 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120555668 | GGGGATAGGCCAGGC[G/T]CGGTGGCTCACACCT | 8450 |
rs780236158 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120577302 | GATACTCTTTACTGT[A/G]TTTAGAAAGCTCTTT | 8450 |
rs780240866 | snp | G/T | 2.73958e-05 | 0.00370096 | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560571 | GTATTACCATCAGTG[G/T]CAGATCTGACCTCCT | 8450 |
rs780355906 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120527803 | AGCATTTCAGATTTT[A/G]GATTCTCATTAAAGG | 8450 |
rs780458825 | in-del | -/T | 0.00212427 | 0.0325211 | intron-variant | CUL4B | GRCh38.p7 | X:120537980 | CTTATATTTCACCAA[-/T]TTTTTTTTCTACTGT | 8450 |
rs780481482 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120532154 | CATCTGCCATTTTTC[A/G]AAGCTATTTAATGGC | 8450 |
rs780536781 | snp | C/G | 0.00211696 | 0.0324653 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120525601 | ATTCTGAAAGGAAAA[C/G]CAGCATGACACAGAA | 8450 |
rs780547974 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120534031 | AGATCGCGCCACTGC[A/G]CTCCAGCCTGGGTGA | 8450 |
rs780553262 | snp | C/T | 0.000675338 | 0.0183634 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558059 | ATGATATGTAAAAGG[C/T]TGGCATCAGAATACC | 8450 |
rs780633963 | snp | A/T | 2.46457e-05 | 0.00351031 | missense | CUL4B | GRCh38.p7 | X:120544120 | TTTAAATACCTCTCT[A/T]TCTTGCATTAATTTT | 8450 |
rs780638313 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120547840 | CAAAAAAAGTGAAAA[G/T]GAGAGAAGGGCCTAG | 8450 |
rs780639513 | snp | G/T | 4.56048e-05 | 0.00477497 | intron-variant | CUL4B | GRCh38.p7 | X:120574522 | TTATTTAGACTTAAC[G/T]CTTGAGTTTTACTAG | 8450 |
rs780640326 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120566705 | CCCAGCCAAATTTCA[C/T]ATTTTTAGCAAAATT | 8450 |
rs780643301 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120530978 | TCCTGTCTTTGATGT[A/G]TATGTGAAAATGACA | 8450 |
rs780712577 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120567801 | GATTGCTTGAGCCCA[A/G]GAGTTCCAGCTGCAG | 8450 |
rs780715336 | in-del | -/A | 0.00738971 | 0.0603345 | intron-variant | CUL4B | GRCh38.p7 | X:120556676 | AGACCCCTATCTCTT[-/A]AAAAAAACAGGAAAA | 8450 |
rs780749145 | snp | G/T | 1.64757e-05 | 0.00287012 | synonymous-codon | CUL4B | GRCh38.p7 | X:120538142 | TTTGAACTGAATCAT[G/T]ATGTCTTTAGAAAGT | 8450 |
rs780755640 | in-del | -/C | 2.40735e-05 | 0.00346932 | frameshift-variant | CUL4B | GRCh38.p7 | X:120535886 | CTGCCACTGAAGTTT[-/C]CCTGCCACTATGTTT | 8450 |
rs780812916 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120559652 | ATAAAAAGATCACTA[C/T]TGCTACCTGCATTTC | 8450 |
rs780834030 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120541896 | AAACCCAACCATCTT[C/T]CTGGGTAAAAACTAA | 8450 |
rs780873097 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120566368 | ATATATATATATATA[A/T]ATATATATATATATA | 8450 |
rs780887931 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120574741 | TATCCTATTTGTTCC[A/C]TATCTTCAAGGAAAT | 8450 |
rs780915958 | snp | C/G | 3.73958e-05 | 0.00432394 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CUL4B | GRCh38.p7 | X:120561435 | CCCAGGTCCGCAGGA[C/G]TTGAGTGGGGGGGGG | 8450 |
rs780970623 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120537058 | AGATCAAAACACACA[C/T]TGAGATCTTAAAACT | 8450 |
rs780975685 | in-del | -/CCGCGGGAAGCTTCGCG | 0.00010295 | 0.00717385 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561339 | CCCTCCTTAACGGTC[-/CCGCGGGAAGCTTCGCG]CCGCGGGAAGCTTCG | 8450 |
rs781003238 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | CUL4B | GRCh38.p7 | X:120557451 | GGTGCGTCTTGTAGC[C/T]CAGGTATTAGAAAAA | 8450 |
rs781026157 | snp | C/T | 4.56106e-05 | 0.00477527 | intron-variant | CUL4B | GRCh38.p7 | X:120574637 | CCTTTGGGTCTACGA[C/T]AGAAAACAGAGAATT | 8450 |
rs781082898 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120568744 | AGATAGATCAAGTAC[C/T]ATCCCCACTGTACAG | 8450 |
rs781117807 | snp | C/T | 2.73538e-05 | 0.00369813 | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560590 | ATCTGACCTCCTGAG[C/T]AGCAGCAGCAGCTGA | 8450 |
rs781150762 | snp | C/G | | | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120562245 | TATCGGCAAAAGTCA[C/G]TGTTTTCTACTAATG | 8450 |
rs781222196 | snp | C/T | 2.28092e-05 | 0.00337699 | synonymous-codon | CUL4B | GRCh38.p7 | X:120530249 | AGTGCTTGCTTGTTC[C/T]TCAACCTAACAAAAA | 8450 |
rs781235741 | snp | A/G | 7.26603e-05 | 0.00602701 | intron-variant | CUL4B | GRCh38.p7 | X:120540333 | TATGACTCAAAGAAC[A/G]TCATTAAACAACTGG | 8450 |
rs781242824 | snp | C/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120575074 | CTGCCTCTTCTTTAA[C/G]CTGCAGTGCTATGGT | 8450 |
rs781251650 | in-del | -/TT | | | intron-variant | CUL4B | GRCh38.p7 | X:120556914 | TGAAGTATATATATA[-/TT]TTTTTTTTTTTTTGA | 8450 |
rs781271338 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120555298 | TAACCACAATAAACA[C/T]TTGTTACAAATATGG | 8450 |
rs781274909 | snp | C/T | 0.000100721 | 0.00709581 | intron-variant | CUL4B | GRCh38.p7 | X:120547123 | TCACGATTTTTTGTT[C/T]TAAAAAGGATATTCT | 8450 |
rs781300018 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120534158 | GAAGACCCCTTGAGC[C/T]CAGGAGTTTGAGACC | 8450 |
rs781301993 | in-del | -/A | 0.00777442 | 0.0618609 | intron-variant | CUL4B | GRCh38.p7 | X:120545527 | CATGATCTGCCAATG[-/A]AAAAAAAAGAAATCA | 8450 |
rs781374527 | snp | C/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120572902 | CTTTGTTTCTTTTTT[C/G]AACTATTAGTGTTTT | 8450 |
rs781390294 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120544400 | CTTGTTATGACATCA[A/G]CACATTACCTGTCTG | 8450 |
rs781476440 | snp | C/T | 0.000529661 | 0.016265 | synonymous-codon | CUL4B | GRCh38.p7 | X:120526764 | AAGGCCAACATTCTA[C/T]GCAATATAGTTGTAC | 8450 |
rs781494616 | snp | C/G | 2.31155e-05 | 0.00339959 | intron-variant | CUL4B | GRCh38.p7 | X:120536906 | TATGCCTATAACTCA[C/G]TTCTAAACAGTAACT | 8450 |
rs781553189 | snp | A/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120530557 | ACCATTTTGTTTTTT[A/T]ACTCTGTCTTTGATA | 8450 |
rs781564283 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120564159 | AATACAAAAATGAGC[C/T]GGACATGGTGGTGTT | 8450 |
rs781636620 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120554826 | TCCCACTCAGGTAGA[C/T]TGAGAGAGTACTTCT | 8450 |
rs781681398 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120525797 | AATCCTAGGAAGCCT[A/G]TAACAATCTACAATT | 8450 |
rs781688194 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | CUL4B | GRCh38.p7 | X:120534875 | GTCATTCTAGATATT[C/T]ATCACAAGCAGCAAG | 8450 |
rs781720263 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120550294 | TATCTATAAGTTCTT[C/T]AATACTTTTTGAGCT | 8450 |
rs781740692 | snp | A/G | 5.64382e-05 | 0.00531186 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558047 | AGGCTTATCTAGATG[A/G]TATGTAAAAGGTTGG | 8450 |
rs781760642 | snp | C/T | 0.00158814 | 0.0281345 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561297 | CCTGGCAGCGCCTTC[C/T]TTCCCTGGCCCACCG | 8450 |
rs781765213 | snp | C/G | 0.000529661 | 0.016265 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560706 | CCTGCGTGCGTGTAG[C/G]AGAGAAGGTAGCAAT | 8450 |
rs781772074 | snp | A/G | 4.66271e-05 | 0.00482819 | synonymous-codon | CUL4B | GRCh38.p7 | X:120547165 | AATCTGTGCTTTGAT[A/G]TGATCTTCGCAGATC | 8450 |
rs786200913 | snp | A/G | | | splice-acceptor-variant | CUL4B | GRCh38.p7 | X:120545519 | TTTTTTTTCATTGGC[A/G]GATCATGATCAGGAG | 8450 |
rs796508522 | in-del | -/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120540039 | TTTCACTGACAACTG[-/T]TAATTTCATGCTGCC | 8450 |
rs796631375 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120554401 | AGTCAATTAAAAACA[A/G]GCACGCAAACAAACA | 8450 |
rs796874376 | snp | A/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120543330 | TTTTTCCAAGTTTTG[A/C]TACTTTTATTAGGAA | 8450 |
rs797044862 | snp | A/G | | | splice-donor-variant | CUL4B | GRCh38.p7 | X:120538659 | CCAAACTTAAACATG[A/G]TAGGTTTCTCATTCT | 8450 |