SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs14279 | snp | C/T | 0 | 0 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120524806 | AAACTTGATGCTGTT[C/T]CAGCTGAAAAATTAG | 8450 |
rs1057116 | snp | A/G | 0.150308 | 0.229263 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120526086 | GAGTATGGGATGTGT[A/G]TATATGGCTTAGCCC | 8450 |
rs1801846 | snp | A/G | | | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120525756 | ATTTTCTCTACCAAA[A/G]TTTTTTTTAGAAGCA | 8450 |
rs2106543 | snp | C/G | 0.490329 | 0.0688607 | intron-variant | CUL4B | GRCh38.p7 | X:120570228 | GTGAGAATCACAAAG[C/G]GGGAGAATAGGGTTT | 8450 |
rs2285549 | snp | C/T | 0.0555816 | 0.157167 | intron-variant | CUL4B | GRCh38.p7 | X:120544033 | TGTTGGGAAGATAAA[C/T]GCAAAGGGAAGCTTA | 8450 |
rs2285550 | snp | A/G | 0.362309 | 0.223353 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120561769 | GGAGTAACCCTAAAT[A/G]GAGGAAAACATAATC | 8450 |
rs2285551 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120562546 | AATTTCCATAACAAT[A/G]ATATGACATATATAC | 8450 |
rs2301636 | snp | C/T | 0.451229 | 0.148347 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120557736 | AAGCACAACTTATAC[C/T]GGTATGACTGTACCC | 8450 |
rs3214123 | in-del | -/AT | | | intron-variant | CUL4B | GRCh38.p7 | X:120543702 | CGACAGTTTAAGACT[-/AT]TAAATTCAGCATGTG | 8450 |
rs3747434 | snp | A/G | 0 | 0 | synonymous-codon | CUL4B | GRCh38.p7 | X:120537005 | CACAGTTAACTCAAT[A/G]TTTCCCGGAACATTC | 8450 |
rs4360414 | snp | C/T | 0.499734 | 0.0115201 | intron-variant | CUL4B | GRCh38.p7 | X:120528232 | GCTAACATGGCAAAA[C/T]CCCATCTGTACTAAA | 8450 |
rs4495565 | snp | A/C | 0 | 0 | intron-variant | CUL4B | GRCh38.p7 | X:120570732 | ATAATGAAATACTAT[A/C]CAGCATTGAACAATG | 8450 |
rs5909729 | snp | C/T | 0.0168099 | 0.0901243 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120563436 | GAGTCAGGGTTTTGC[C/T]ATGTTGGCCAGGCTG | 8450 |
rs5909731 | snp | A/T | 0.245924 | 0.249967 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120576347 | TTTCTGCATGTTTGA[A/T]CATTTTTATAACAAA | 8450 |
rs5909732 | snp | A/C | 0.254536 | 0.249959 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120577657 | TCTATACTCATTGCA[A/C]TCATTTATAAGGAAT | 8450 |
rs5910904 | snp | C/T | 0.441884 | 0.160251 | intron-variant | CUL4B | GRCh38.p7 | X:120548748 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG | 8450 |
rs5910908 | snp | C/T | 0.420529 | 0.182811 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120563169 | CGCTGAGAAGGGAGA[C/T]GGGGGCCTGAAAGGA | 8450 |
rs5910909 | snp | C/T | 0.286116 | 0.247378 | intron-variant | CUL4B | GRCh38.p7 | X:120564353 | gctcaggcttgtaat[C/T]ccaaaactttgggag | 8450 |
rs5910915 | snp | C/T | 0.254536 | 0.249959 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120577355 | tgtctgtaattccag[C/T]gctttgggaggccga | 8450 |
rs5910916 | snp | A/G | 0.078261 | 0.181675 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120577369 | gcgctttgggaggcc[A/G]aggtaggtggattga | 8450 |
rs5956224 | snp | A/C | 0.109764 | 0.206963 | intron-variant | CUL4B | GRCh38.p7 | X:120535123 | tagcttgagcccatg[A/C]gtttgaggttacagt | 8450 |
rs5956225 | snp | A/G | 0.132653 | 0.220748 | intron-variant | CUL4B | GRCh38.p7 | X:120552127 | catattatgcattac[A/G]tatttattatttaCA | 8450 |
rs5956226 | snp | C/T | 0.440613 | 0.161761 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120558779 | AAGTTTTAATTAGAA[C/T]ATCCAAATGCCTTAA | 8450 |
rs5957406 | snp | C/T | 0.110699 | 0.207594 | intron-variant | CUL4B | GRCh38.p7 | X:120526946 | AAAAGACAACAGTTT[C/T]GGCTCATGAATTTAA | 8450 |
rs5957407 | snp | C/T | 0.0768 | 0.180282 | intron-variant | CUL4B | GRCh38.p7 | X:120540702 | aagatggaatcttgc[C/T]atgttgcccaggcta | 8450 |
rs5957408 | snp | C/T | 0.0983752 | 0.198771 | intron-variant | CUL4B | GRCh38.p7 | X:120543829 | AAAGATAGTTTTTTA[C/T]ATTATTGTTTTCCTC | 8450 |
rs5957411 | snp | A/G | 0.0560809 | 0.157783 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120563164 | AGAACCGCTGAGAAG[A/G]GAGATGGGGGCCTGA | 8450 |
rs5957412 | snp | A/G | 0.0831127 | 0.186141 | upstream-variant-2KB, intron-variant | CUL4B | GRCh38.p7 | X:120563186 | GGGGCCTGAAAGGAG[A/G]CAGATGGAAGCACTC | 8450 |
rs6603633 | snp | A/C | 0.110232 | 0.207279 | intron-variant | CUL4B | GRCh38.p7 | X:120530932 | CATAAATGTTTTAAA[A/C]GTAAGGACATGGTAA | 8450 |
rs6645657 | snp | C/T | 0.139594 | 0.2243 | intron-variant | CUL4B | GRCh38.p7 | X:120546951 | TACATGAATACCACA[C/T]GTAGTCCTGGACACG | 8450 |
rs6646682 | snp | A/C | 0.0550819 | 0.156547 | intron-variant | CUL4B | GRCh38.p7 | X:120544963 | TCTAAGACATAAAAC[A/C]GTTTTCACTGTACTG | 8450 |
rs6646683 | snp | C/T | 0 | 0 | intron-variant | CUL4B | GRCh38.p7 | X:120553451 | TTCACAAAAAGGTAA[C/T]TACAGTTCCCattat | 8450 |
rs6655533 | snp | A/G | 0.112567 | 0.208835 | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120559365 | TAATACTCTCCTCAC[A/G]TATCTCAAACACGGT | 8450 |
rs7049515 | snp | C/T | 0.405517 | 0.195741 | intron-variant | CUL4B | GRCh38.p7 | X:120569383 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 8450 |
rs7057136 | snp | C/T | 0.0328205 | 0.123827 | intron-variant | CUL4B | GRCh38.p7 | X:120536509 | CCTATGGGTGAAATA[C/T]GTGCAAGAATTCTTA | 8450 |
rs7879339 | snp | A/G | 0.0699487 | 0.17344 | intron-variant | CUL4B | GRCh38.p7 | X:120566369 | TATATATATATATAT[A/G]TATATATATATATAT | 8450 |
rs7879694 | snp | A/G | 0.485039 | 0.0851863 | intron-variant | CUL4B | GRCh38.p7 | X:120573857 | ttgagacggagtccc[A/G]ctgttgcccaggctg | 8450 |
rs7881300 | snp | A/G | 0 | 0 | intron-variant | CUL4B | GRCh38.p7 | X:120549634 | CACCACACCTCATCA[A/G]GAAACAGCAGGCCAA | 8450 |
rs11549411 | snp | G/T | 0.0116955 | 0.0755709 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120524709 | GAACAACAACTGAAA[G/T]TCACAATTATCCAAT | 8450 |
rs11796393 | snp | C/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120536521 | ATATGTGCAAGAATT[C/T]TTAATAGCTAGGTAG | 8450 |
rs11796939 | snp | A/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120538437 | AAAATAAATGGGAAA[A/T]TTTTATACAAATAAT | 8450 |
rs12011507 | snp | G/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120569563 | gacggggtttcaccg[G/T]gttagccaggatggt | 8450 |
rs12387747 | snp | C/T | 0.0879364 | 0.190356 | intron-variant | CUL4B | GRCh38.p7 | X:120530961 | AATCCTTTAAGAAAA[C/T]ATCCTGTCTTTGATG | 8450 |
rs12392620 | snp | A/C | 0.108827 | 0.206325 | intron-variant | CUL4B | GRCh38.p7 | X:120574106 | ccatcacctgccccc[A/C]tctgccccagcctcc | 8450 |
rs12393998 | snp | A/C | 0.491747 | 0.063706 | intron-variant | CUL4B | GRCh38.p7 | X:120566227 | CAATGTGAATTCATC[A/C]GTTTCCCATCCTGAG | 8450 |
rs12396563 | snp | C/G | 0.149865 | 0.22907 | intron-variant | CUL4B | GRCh38.p7 | X:120552013 | TGAAAAGCACTttta[C/G]aaatatattctttta | 8450 |
rs12688345 | snp | C/T | 0.49952 | 0.0154892 | intron-variant | CUL4B | GRCh38.p7 | X:120530690 | CATGGTATTAACTGG[C/T]TAAGCAAACTAGTTA | 8450 |
rs12837257 | snp | A/T | 0 | 0 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120577152 | CTTTTCTCTTTCTTT[A/T]AGATTTATACAGCTT | 8450 |
rs12839503 | snp | A/G | 0.0912962 | 0.193166 | intron-variant | CUL4B | GRCh38.p7 | X:120571097 | tgctctaggggaagt[A/G]tgggaggaaaattta | 8450 |
rs12842985 | snp | C/T | 0.0490645 | 0.148745 | intron-variant | CUL4B | GRCh38.p7 | X:120575365 | TTCCTAAACAAGATC[C/T]TCCCCACATTCCGAA | 8450 |
rs12858999 | snp | C/T | 0 | 0 | upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120576112 | ttgctagattgctcc[C/T]ttttgggttctttgt | 8450 |
rs17853573 | snp | G/T | 0.0110494 | 0.0735024 | missense | CUL4B | GRCh38.p7 | X:120535865 | ACACACAGTGTCCTA[G/T]GGTTGACTGCCACTG | 8450 |
rs28460170 | snp | A/C | 0.108827 | 0.206325 | intron-variant | CUL4B | GRCh38.p7 | X:120572622 | ATTAAAGATCTTTTT[A/C]TATACACTTAACCAA | 8450 |
rs28528673 | snp | A/T | 0.108827 | 0.206325 | intron-variant | CUL4B | GRCh38.p7 | X:120573129 | GTTAAATTTGGTGCA[A/T]CACCTTCCTCAGCAT | 8450 |
rs28590057 | snp | A/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120548339 | GCTTCATTTTGGGTT[A/T]AAAAAAGAATTTCAC | 8450 |
rs34111189 | snp | A/G | 0.0505727 | 0.150761 | intron-variant | CUL4B | GRCh38.p7 | X:120566020 | GGCGTGAGCCACCGC[A/G]CCCGGCCCAGGCAGT | 8450 |
rs34722195 | in-del | -/A | | | intron-variant | CUL4B | GRCh38.p7 | X:120543052 | AAGGAAAAAAAAAAA[-/A]GGTTAGTATTATTGA | 8450 |
rs34777683 | in-del | -/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120536115 | ACCAAATCAAATGGG[-/G]ATTTATTAGGATTTA | 8450 |
rs34930174 | in-del | -/C | | | intron-variant | CUL4B | GRCh38.p7 | X:120570907 | AAGTATAGAAGGAAA[-/C]ATAGCTGGGTGATAT | 8450 |
rs35048954 | snp | C/T | 0.00202198 | 0.0317317 | intron-variant | CUL4B | GRCh38.p7 | X:120546638 | CATATGTTAAGGATA[C/T]TTTAAAGCGTTTGGT | 8450 |
rs35267132 | in-del | -/C | | | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120526446 | AAGAACCCTCCCCCC[-/C]TTTTTAATAGCCACA | 8450 |
rs35644958 | in-del | -/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120555666 | TGGGGATAGGCCAGG[-/G]CGCGGTGGCTCACAC | 8450 |
rs35746806 | in-del | -/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120543704 | ACAGTTTAAGACTAT[-/T]AAATTCAGCATGTGG | 8450 |
rs35976026 | in-del | -/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120543999 | AAGGAGCACCTAAGT[-/T]GAGAGAAGAGCATCA | 8450 |
rs45437794 | snp | C/T | 0.0317957 | 0.122012 | utr-variant-5-prime | CUL4B | GRCh38.p7 | X:120575712 | CCAAAGCCTGGGTTA[C/T]TCTCTAATAATACTA | 8450 |
rs45524842 | snp | A/G | 0.0204488 | 0.0990265 | utr-variant-5-prime | CUL4B | GRCh38.p7 | X:120575744 | CTATGGGACTTAAAC[A/G]GATAAGCCTAGGTTG | 8450 |
rs45549338 | snp | A/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120540703 | AGATGGAATCTTGCT[A/T]TGTTGCCCAGGCTAG | 8450 |
rs55848212 | snp | C/T | | | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120524970 | CATCTCACAGACCAT[C/T]AGGGATGAGTTAGAA | 8450 |
rs56016419 | snp | A/G | 0.00581083 | 0.0535878 | intron-variant | CUL4B | GRCh38.p7 | X:120534350 | ACAGAGTGAGACCCT[A/G]TCTCATTAAAAAAAA | 8450 |
rs56144145 | snp | G/T | 0.255278 | 0.249944 | intron-variant | CUL4B | GRCh38.p7 | X:120570738 | AAATACTATACAGCA[G/T]TGAACAATGAATAAA | 8450 |
rs56241821 | snp | A/G | 0.39608 | 0.202881 | intron-variant | CUL4B | GRCh38.p7 | X:120554724 | TCAGAGAAAGAGGGT[A/G]GGACAGGGGTTTGGA | 8450 |
rs57119187 | snp | C/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120539056 | TATTTAAGAGATTAA[C/G]CCAAGTAGCAAAAAT | 8450 |
rs58096878 | snp | A/C | 0.0261392 | 0.111294 | utr-variant-3-prime | CUL4B | GRCh38.p7 | X:120525918 | TTACAAAACACGTTC[A/C]TTTTGGTCTCTTTTG | 8450 |
rs58242779 | snp | C/T | | | intron-variant, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120557845 | AGTCTACTTAAGAAC[C/T]TATTTCAGAAAGCAA | 8450 |
rs58763492 | in-del | -/GT | | | intron-variant | CUL4B | GRCh38.p7 | X:120566346 | TGTGTGTGTATAGGT[-/GT]ATATATATATATATA | 8450 |
rs59022882 | in-del | -/A | 0.00949095 | 0.0682305 | intron-variant | CUL4B | GRCh38.p7 | X:120556913 | CTGAAGTATATATAT[-/A]TTTTTTTTTTTTTTT | 8450 |
rs59133588 | snp | A/G | | | intron-variant | CUL4B | GRCh38.p7 | X:120565451 | CACTTTGGGAGGCCA[A/G]AGTGGGTGGATCACT | 8450 |
rs60058698 | in-del | -/ACAC | | | intron-variant | CUL4B | GRCh38.p7 | X:120543530 | CACACACACACACAC[-/ACAC]CCCTAATAATCGAAT | 8450 |
rs60471809 | in-del | -/ATATAT | | | intron-variant | CUL4B | GRCh38.p7 | X:120566390 | TATATATATATATAT[-/ATATAT]GTATATATATTTGGG | 8450 |
rs61390830 | in-del | -/ACACACAC | | | intron-variant | CUL4B | GRCh38.p7 | X:120543526 | CACACACACACACAC[-/ACACACAC]CCCTAATAATCGAAT | 8450 |
rs61752964 | snp | C/T | | | synonymous-codon | CUL4B | GRCh38.p7 | X:120535887 | CTGCCACTGAAGTTT[C/T]CTGCCACTATGTTTG | 8450 |
rs61752965 | snp | A/C/T | | | missense | CUL4B | GRCh38.p7 | X:120535891 | CACTGAAGTTTCCTG[A/C/T]CACTATGTTTGCCTA | 8450 |
rs61754550 | snp | A/G | 2.33926e-05 | 0.00341991 | missense | CUL4B | GRCh38.p7 | X:120544638 | AATAACTCCAGTCCC[A/G]TGTCCCTAAAATAAA | 8450 |
rs61757196 | snp | C/T | | | synonymous-codon | CUL4B | GRCh38.p7 | X:120547234 | AGAACAGAGATTTTC[C/T]ACAGCCTGCAAGGTT | 8450 |
rs61759504 | snp | A/G | | | missense, upstream-variant-2KB | CUL4B | GRCh38.p7 | X:120560385 | GCCACTGAAACCCCC[A/G]GGCAGAAGGACGAGG | 8450 |
rs62616188 | snp | A/G | 0.0142023 | 0.083063 | intron-variant | CUL4B | GRCh38.p7 | X:120566994 | ATGTGCCATGGCATG[A/G]GCCTATTTTTAACAT | 8450 |
rs62616189 | snp | C/T | 0.492017 | 0.0626724 | intron-variant | CUL4B | GRCh38.p7 | X:120567323 | GTAGAAATGGGGTTT[C/T]GCCATGTTGGCCAGG | 8450 |
rs62616190 | snp | C/T | 0.381341 | 0.212719 | intron-variant | CUL4B | GRCh38.p7 | X:120568269 | ATTTTGCTGACCTCA[C/T]AGTATTGCCTAGGGC | 8450 |
rs66749436 | in-del | -/A | | | intron-variant | CUL4B | GRCh38.p7 | X:120572483 | AAAAAAAAAAAAAAA[-/A]GAAAAAGAAAAGAAA | 8450 |
rs67116649 | in-del | -/TA | | | intron-variant | CUL4B | GRCh38.p7 | X:120556904 | TATTGTACTCTGAAG[-/TA]TATATATATTTTTTT | 8450 |
rs71820203 | in-del | -/A | | | intron-variant | CUL4B | GRCh38.p7 | X:120535705 | TGAGACTCTGTCTCA[-/A]AAAAAAAAAAAAAAA | 8450 |
rs71840531 | in-del | -/TA | 0.145386 | 0.227059 | intron-variant | CUL4B | GRCh38.p7 | X:120543701 | ACGACAGTTTAAGAC[-/TA]TTAAATTCAGCATGT | 8450 |
rs72098040 | in-del | -/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120556914 | TGAAGTATATATATA[-/T]TTTTTTTTTTTTTTG | 8450 |
rs72483160 | in-del | -/T | | | intron-variant | CUL4B | GRCh38.p7 | X:120567141 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTTTGGC | 8450 |
rs73219157 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | CUL4B | GRCh38.p7 | X:120533301 | TTGATCCTTCCAGTT[A/G]CCCTGTAGATTGATT | 8450 |
rs73219159 | snp | A/G/T | 0.0550819 | 0.156547 | intron-variant | CUL4B | GRCh38.p7 | X:120546249 | GAGTGGGAGGGGGGC[A/G/T]AGGGATAAAAGACTA | 8450 |
rs73620006 | snp | C/G | 0.0131573 | 0.0800346 | intron-variant | CUL4B | GRCh38.p7 | X:120550648 | TGGAGGGTGGTTTAA[C/G]AACTTTAAGGCAAGA | 8450 |
rs73639317 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120540945 | TTATTAGAAGCCTCT[A/G]GGATCTTTTCCTTAT | 8450 |
rs73639318 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | CUL4B | GRCh38.p7 | X:120549647 | CAGGAAACAGCAGGC[C/T]AATTAGATTGAGCAG | 8450 |
rs73639319 | snp | A/G | 0.0772873 | 0.180749 | intron-variant | CUL4B | GRCh38.p7 | X:120554758 | CTTTTGTATAACTAC[A/G]TATTTCCACATTATT | 8450 |