SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1717 | snp | C/G | 0.130351 | 0.219509 | utr-variant-3-prime | FBXO32 | GRCh38.p7 | 8:123500357 | CTTCATATTTGACAT[C/G]TATTTTGAAATTCTG | 114907 |
rs1043602 | snp | A/C | | | utr-variant-3-prime | FBXO32 | GRCh38.p7 | 8:123498874 | CACTTAATGTTTTCA[A/C]AGACCTCTGATTCTG | 114907 |
rs1048515 | snp | C/T | 0.491783 | 0.0635686 | utr-variant-3-prime | FBXO32 | GRCh38.p7 | 8:123502529 | AGTCCCAGGGGAGGA[C/T]TGCTTGAGCCCAGGA | 114907 |
rs1048593 | snp | C/T | | | synonymous-codon | FBXO32 | GRCh38.p7 | 8:123503376 | CAACTTGTTCAAGTT[C/T]TGAATCCCAGCCCAT | 114907 |
rs2280915 | snp | C/T | 0.222035 | 0.248431 | utr-variant-3-prime | FBXO32 | GRCh38.p7 | 8:123498034 | AGGACTCAGCTCACA[C/T]AATATTAAATAAACA | 114907 |
rs2280919 | snp | A/G | 0.474 | 0.111014 | intron-variant | FBXO32 | GRCh38.p7 | 8:123539539 | CCAAGTAACTCCAAC[A/G]TAAATGGTTATATGC | 114907 |
rs2280920 | snp | A/G | 0.439085 | 0.163545 | intron-variant | FBXO32 | GRCh38.p7 | 8:123539582 | CGCTCAAGTCTCTCC[A/G]GACAGACCCCCAGAA | 114907 |
rs2280921 | snp | C/G | 0.437118 | 0.165792 | intron-variant | FBXO32 | GRCh38.p7 | 8:123539920 | ACTTTCATCGCCCCC[C/G]CTCACCGGGCTAAAT | 114907 |
rs2294088 | snp | A/G | 0.464939 | 0.127677 | intron-variant | FBXO32 | GRCh38.p7 | 8:123514367 | GTTGCCAGGCTTAGA[A/G]TACAGAGATATTTTT | 114907 |
rs2294089 | snp | C/T | 0.359998 | 0.2245 | intron-variant | FBXO32 | GRCh38.p7 | 8:123514523 | TTCAAAACCCAGGAT[C/T]GGGTTGAATATTTAA | 114907 |
rs2294090 | snp | C/T | 0.491368 | 0.0651254 | intron-variant, upstream-variant-2KB | FBXO32 | GRCh38.p7 | 8:123532907 | CATATTATTATATTG[C/T]CCTGGGTTTTGCCTC | 114907 |
rs2385270 | snp | A/G | 0.220544 | 0.248259 | intron-variant | FBXO32 | GRCh38.p7 | 8:123512952 | AAAAGCCAAGTTTCC[A/G]GCTTTCCCATAATAG | 114907 |
rs2385271 | snp | C/T | 0 | 0 | intron-variant | FBXO32 | GRCh38.p7 | 8:123506892 | CAATTACAAGGTTCG[C/T]TGCTTTCCTGAAGGC | 114907 |
rs2385272 | snp | A/T | 0.0150367 | 0.0853947 | intron-variant | FBXO32 | GRCh38.p7 | 8:123530396 | GTGGTTGGTTTGGTT[A/T]TTATTTTCTTTTTCC | 114907 |
rs2385275 | snp | C/T | | | utr-variant-3-prime | FBXO32 | GRCh38.p7 | 8:123499895 | ACACTAGAGCAGGTT[C/T]TACTAGCACTTGGGC | 114907 |
rs2385276 | snp | C/T | 0.0908922 | 0.192833 | intron-variant | FBXO32 | GRCh38.p7 | 8:123518964 | catagtgctgtgccc[C/T]tgtggtcccagctac | 114907 |
rs2385277 | snp | C/G | 0.445328 | 0.156035 | intron-variant | FBXO32 | GRCh38.p7 | 8:123518703 | TGGTTAAATGGAGAA[C/G]CTATCTCACTGGGTT | 114907 |
rs2385278 | snp | A/G | 0 | 0 | intron-variant | FBXO32 | GRCh38.p7 | 8:123518563 | TAGAAAAACTATGCA[A/G]GTCATAAAATGTATC | 114907 |
rs2385279 | snp | A/G | 0 | 0 | intron-variant | FBXO32 | GRCh38.p7 | 8:123516166 | ATATTTTCCTGTGTT[A/G]AGAAGGACTCTGCTG | 114907 |
rs2385291 | snp | A/G | 0.490997 | 0.0664859 | intron-variant | FBXO32 | GRCh38.p7 | 8:123524582 | TGCCACCATCCTGCA[A/G]CCTGGGTAACAGAGG | 114907 |
rs2385292 | snp | A/C | 0 | 0 | intron-variant | FBXO32 | GRCh38.p7 | 8:123524148 | AAGAAGTAGGAGGGT[A/C]CCCACAGAAATTAGG | 114907 |
rs2385293 | snp | G/T | 0 | 0 | intron-variant | FBXO32 | GRCh38.p7 | 8:123521947 | ATCTGTGTTATTCAT[G/T]GAGTAAATAAGGGTC | 114907 |
rs2385343 | snp | C/T | 0 | 0 | intron-variant | FBXO32 | GRCh38.p7 | 8:123509820 | CTTCCTCCCACTGTC[C/T]TCTGTCCCAACCCTC | 114907 |
rs2891735 | snp | C/T | 0 | 0 | intron-variant | FBXO32 | GRCh38.p7 | 8:123512822 | GCCTTCCCAGCTTTA[C/T]TGTATTCAAGACAGC | 114907 |
rs2891736 | snp | C/T | 0 | 0 | intron-variant | FBXO32 | GRCh38.p7 | 8:123512847 | GACAGCAACCTAAGG[C/T]TGCAAACAACTCATG | 114907 |
rs2891737 | snp | C/T | | | utr-variant-3-prime | FBXO32 | GRCh38.p7 | 8:123499853 | GGGTGTGTATTATGC[C/T]ATTGCCATAGTTCTC | 114907 |
rs2891739 | snp | C/T | | | intron-variant | FBXO32 | GRCh38.p7 | 8:123535243 | AAGCTGCTGCTGCTT[C/T]TTTAGAAAAAAAAAA | 114907 |
rs3739284 | snp | A/G | 0.492037 | 0.0625946 | utr-variant-3-prime | FBXO32 | GRCh38.p7 | 8:123502160 | AAAATGAGTCCATCT[A/G]AGCTAGGGCTTTTTG | 114907 |
rs3739285 | snp | C/G | 0.163564 | 0.234582 | utr-variant-3-prime | FBXO32 | GRCh38.p7 | 8:123502021 | CCAAGGGGATCTTAC[C/G]AGGCAAATATCAGCA | 114907 |
rs3739286 | snp | A/G | 0.474634 | 0.109726 | utr-variant-3-prime | FBXO32 | GRCh38.p7 | 8:123501943 | AAAATATTCCTGGGA[A/G]TAGATGGGGGATCTA | 114907 |
rs3739287 | snp | A/G | 0.232159 | 0.249368 | intron-variant, synonymous-codon | FBXO32 | GRCh38.p7 | 8:123513243 | GTATCGGATGGAGAC[A/G]ATTCTCCACTGGCAG | 114907 |
rs3739288 | snp | A/C | 0.34146 | 0.23267 | intron-variant | FBXO32 | GRCh38.p7 | 8:123513137 | AGGGATACTGGACAG[A/C]CTCGCCAAGACTTTG | 114907 |
rs3892087 | snp | A/G | 0.00284761 | 0.0376258 | intron-variant, synonymous-codon | FBXO32 | GRCh38.p7 | 8:123513306 | CTTGCCGACTCTTTG[A/G]ACCAGTGTACATAAG | 114907 |
rs4242341 | snp | C/T | 0.455383 | 0.142541 | intron-variant | FBXO32 | GRCh38.p7 | 8:123528404 | CTGGAATCCTTCCAG[C/T]TCCTCAAGGGAATTT | 114907 |
rs4380919 | snp | C/T | | | intron-variant | FBXO32 | GRCh38.p7 | 8:123512790 | TTAAAAGGCTGGTAC[C/T]AGTTCTCCAAGCTAC | 114907 |
rs4436105 | snp | A/G | 0.409212 | 0.192748 | intron-variant | FBXO32 | GRCh38.p7 | 8:123536196 | TTCCTTCATAAGGCC[A/G]TGCTTAATACCATTT | 114907 |
rs4870855 | snp | A/G | 0.325563 | 0.238307 | intron-variant | FBXO32 | GRCh38.p7 | 8:123503614 | TCGTATGTGGGAGCT[A/G]TGAAAGTAGATTTCA | 114907 |
rs4871383 | snp | C/T | 0.491421 | 0.0649309 | utr-variant-3-prime | FBXO32 | GRCh38.p7 | 8:123502476 | GGAGACAGGCTGGAG[C/T]GCAGTGGCACAATCA | 114907 |
rs4871384 | snp | A/G | 0.381891 | 0.212379 | intron-variant | FBXO32 | GRCh38.p7 | 8:123528585 | AGGGCCAATGCATGT[A/G]GCTTGTAGCCAGTGA | 114907 |
rs4871385 | snp | C/G | 0.289892 | 0.246797 | synonymous-codon | FBXO32 | GRCh38.p7 | 8:123540982 | CACCCAGTTCTGCCC[C/G]GGGGACCGCCAGTCC | 114907 |
rs6470154 | snp | G/T | 0.462582 | 0.131564 | upstream-variant-2KB | FBXO32 | GRCh38.p7 | 8:123542995 | ATTATGAACAATGTG[G/T]GTTAGTTATGTATTA | 114907 |
rs6980508 | snp | A/C | 0.274929 | 0.248754 | intron-variant | FBXO32 | GRCh38.p7 | 8:123537573 | AAAGCTGTGACGTGC[A/C]CCCAGAGGTTTAATT | 114907 |
rs6983670 | snp | A/C | 0.21845 | 0.248001 | upstream-variant-2KB | FBXO32 | GRCh38.p7 | 8:123543244 | TCTTCCCTCCTTTCC[A/C]GTAGCGTCATGTGCC | 114907 |
rs6984753 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FBXO32 | GRCh38.p7 | 8:123537951 | GGTGGTTGCTGAGGA[A/G]GGCTGTGCGGGTGCC | 114907 |
rs6988439 | snp | G/T | 0.42803 | 0.175514 | intron-variant | FBXO32 | GRCh38.p7 | 8:123510513 | agctaccggggagtc[G/T]aaggtagaagaatca | 114907 |
rs6988591 | snp | C/T | 0.0399862 | 0.135625 | missense | FBXO32 | GRCh38.p7 | 8:123534764 | GCTGCAACATCATAG[C/T]TCAGGCTGTTGAAAA | 114907 |
rs6990407 | snp | C/G | 0.42666 | 0.176893 | utr-variant-3-prime | FBXO32 | GRCh38.p7 | 8:123501738 | CCAGGTCACCCAAAG[C/G]TCAGCTCTTAAAGAT | 114907 |
rs7000759 | snp | A/G | 0.093417 | 0.194889 | intron-variant | FBXO32 | GRCh38.p7 | 8:123516436 | CCAGGCCTCAGCCCA[A/G]CTTCATTTCAGATCA | 114907 |
rs7013375 | snp | C/T | 0.218151 | 0.247963 | downstream-variant-500B | FBXO32 | GRCh38.p7 | 8:123497420 | aggtgtgagccactg[C/T]acctggGCCCTCTTT | 114907 |
rs7460236 | snp | A/C | 0.436123 | 0.166908 | intron-variant | FBXO32 | GRCh38.p7 | 8:123530915 | agccaatgcacccag[A/C]cTTTTTTTTTTTTTC | 114907 |
rs7818812 | snp | C/T | 0.38286 | 0.211774 | intron-variant | FBXO32 | GRCh38.p7 | 8:123526350 | CCTGCCTCAGCGTCC[C/T]GAGTAGCTGGGATTA | 114907 |
rs7821824 | snp | A/G | 0.172674 | 0.237741 | intron-variant | FBXO32 | GRCh38.p7 | 8:123539468 | TAAATAAATTACTTG[A/G]TTTTACGTAAATAAG | 114907 |
rs7824506 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | FBXO32 | GRCh38.p7 | 8:123514713 | ATTCTTCTGCCCCCG[C/T]TTGAACTTCTTCCTT | 114907 |
rs7824760 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | FBXO32 | GRCh38.p7 | 8:123514712 | AATTCTTCTGCCCCC[A/G]CTTGAACTTCTTCCT | 114907 |
rs7827149 | snp | C/T | 0.363776 | 0.222609 | intron-variant | FBXO32 | GRCh38.p7 | 8:123524208 | GGGCATCTCCCACTT[C/T]TTCAGGTGGCCTCCT | 114907 |
rs7830622 | snp | C/T | 0.131038 | 0.219882 | intron-variant | FBXO32 | GRCh38.p7 | 8:123530245 | TTTATCAGGTCACTT[C/T]GGACAGCCAAGCCTG | 114907 |
rs7834179 | snp | A/G | 0.139903 | 0.224452 | intron-variant | FBXO32 | GRCh38.p7 | 8:123516764 | TTTCCACATGCAGGG[A/G]GAGATGAGGCTAGCT | 114907 |
rs7834818 | snp | A/G | 0.490943 | 0.0666801 | intron-variant | FBXO32 | GRCh38.p7 | 8:123517137 | TTTTGAAGGGCAGTC[A/G]GCTGTGCACTGTGAC | 114907 |
rs7835298 | snp | A/G | 0.472522 | 0.113946 | intron-variant | FBXO32 | GRCh38.p7 | 8:123540063 | GACCTCAGGTTTCCC[A/G]CCAGACCACAGAGCT | 114907 |
rs9643180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXO32 | GRCh38.p7 | 8:123506710 | TCGAAAGCAGTAGTA[A/G]ATCTCCCCATCCTAA | 114907 |
rs9643181 | snp | C/G | 0.183886 | 0.241099 | intron-variant | FBXO32 | GRCh38.p7 | 8:123508350 | CGAGGTGGGGAGGGA[C/G]CAGTGGCAAGGGGCC | 114907 |
rs9656945 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXO32 | GRCh38.p7 | 8:123527351 | ACAGATACTAAATAA[C/T]GGTTGCTTTCATGCC | 114907 |
rs9694707 | snp | C/G/T | 0.0342917 | 0.127249 | intron-variant | FBXO32 | GRCh38.p7 | 8:123521012 | aggtctcagttcaaa[C/G/T]gtggcctgccccggg | 114907 |
rs10086151 | snp | A/G | 0.463559 | 0.129972 | intron-variant | FBXO32 | GRCh38.p7 | 8:123529040 | AAAACCTCAAAACAC[A/G]GTGGCTATCATTAAA | 114907 |
rs10087726 | snp | C/G | 0.443598 | 0.158176 | intron-variant | FBXO32 | GRCh38.p7 | 8:123509681 | CTCTAGCTTGGGCAA[C/G]GGGAATAAGACCCTA | 114907 |
rs10089389 | snp | C/T | 0.114738 | 0.210248 | intron-variant | FBXO32 | GRCh38.p7 | 8:123505235 | ACAAACTTGAGGCAG[C/T]ATGATGAAGGGAAAC | 114907 |
rs10089663 | snp | A/G | 0.496616 | 0.0409947 | intron-variant | FBXO32 | GRCh38.p7 | 8:123505534 | tgaggtcaggagttc[A/G]agaccagcctggcca | 114907 |
rs10092779 | snp | C/T | 0.496483 | 0.0417852 | intron-variant | FBXO32 | GRCh38.p7 | 8:123505697 | gctgaaactgcacca[C/T]tgtactccagcctgg | 114907 |
rs10093411 | snp | A/G | 0.496517 | 0.0415876 | intron-variant | FBXO32 | GRCh38.p7 | 8:123506290 | ACCAGGGAACCTGGA[A/G]TAGGGGGAACCCAGA | 114907 |
rs10096950 | snp | C/G/T | 0.00676609 | 0.0577691 | intron-variant | FBXO32 | GRCh38.p7 | 8:123506853 | AGACTCTCCAAATAG[C/G/T]GCATGTGCTTTACTC | 114907 |
rs10097344 | snp | C/G | 0 | 0 | intron-variant | FBXO32 | GRCh38.p7 | 8:123530080 | ACTTGCAGAGTCACA[C/G]TGAATGGCATGAACA | 114907 |
rs10101306 | snp | C/T | 0.187053 | 0.241946 | intron-variant | FBXO32 | GRCh38.p7 | 8:123531011 | ttacatggagtctca[C/T]tcctgttgcccaggc | 114907 |
rs10101504 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FBXO32 | GRCh38.p7 | 8:123538418 | TTCACGGTCCCTCCC[A/C]GCTTAAGGGCCTGCC | 114907 |
rs10101794 | snp | C/T | 0.497091 | 0.0380279 | intron-variant | FBXO32 | GRCh38.p7 | 8:123529524 | CAGAGGAGGAAACCA[C/T]GTCTTAGGGAGGTTG | 114907 |
rs10111521 | snp | A/C | 0.492679 | 0.0600586 | intron-variant | FBXO32 | GRCh38.p7 | 8:123515956 | GAGATCGTGCCATTG[A/C]ACTCTCGCCTGGGCA | 114907 |
rs10112369 | snp | G/T | 0.11963 | 0.213316 | intron-variant | FBXO32 | GRCh38.p7 | 8:123507440 | GACTCTGTGCTAGGg[G/T]gtgtgtgtgtgtgtg | 114907 |
rs10113238 | snp | C/G | 0.497473 | 0.0354532 | intron-variant, upstream-variant-2KB | FBXO32 | GRCh38.p7 | 8:123534073 | CTCCAGCCTGGGTGA[C/G]AGAGCAAGACTCTGT | 114907 |
rs10956136 | snp | C/T | 0.455977 | 0.141681 | intron-variant | FBXO32 | GRCh38.p7 | 8:123504291 | AATGAAAAAATTTTA[C/T]AAGTCTGGAAAAACT | 114907 |
rs11347407 | in-del | -/T | 0.121369 | 0.214369 | intron-variant | FBXO32 | GRCh38.p7 | 8:123518836 | AGAGAACACATTTTC[-/T]TTTTTTTTTGTTGAG | 114907 |
rs11459120 | in-del | -/T | 0.273856 | 0.248859 | intron-variant | FBXO32 | GRCh38.p7 | 8:123535096 | TTTGACACACAGCAC[-/T]TGTACTCTTCAACTA | 114907 |
rs11539318 | snp | C/T | | | utr-variant-3-prime | FBXO32 | GRCh38.p7 | 8:123498567 | ATGTTCATTCTCCAC[C/T]AAAACTTCATCCTTT | 114907 |
rs11546887 | snp | A/G | | | utr-variant-3-prime | FBXO32 | GRCh38.p7 | 8:123503131 | GCTGGCAAATTGTTA[A/G]AAAAAAAGTTTATTT | 114907 |
rs11774297 | snp | C/T | 0.355525 | 0.226637 | intron-variant | FBXO32 | GRCh38.p7 | 8:123530673 | CAGGCTGGAGTGCAA[C/T]GGCGCCATCTCGCTC | 114907 |
rs11786471 | snp | C/G | 0.00486615 | 0.0490856 | missense, upstream-variant-2KB | FBXO32 | GRCh38.p7 | 8:123533204 | ACCTCTTTAGTACTT[C/G]CTTTGTGAACATAGA | 114907 |
rs11984925 | snp | A/C | 0.0448719 | 0.142907 | intron-variant | FBXO32 | GRCh38.p7 | 8:123540011 | GCGTACTAGCCGGCG[A/C]TGGCATCGTTAGCCA | 114907 |
rs11986010 | snp | A/G | 0.111576 | 0.20818 | intron-variant | FBXO32 | GRCh38.p7 | 8:123518394 | ACAGGGCAAAGTGCA[A/G]CCCATTTAAAGACCT | 114907 |
rs11986300 | snp | C/G | 0.0883596 | 0.190715 | intron-variant | FBXO32 | GRCh38.p7 | 8:123506103 | gtgttgtggcatgag[C/G]ctgtagtcccagcta | 114907 |
rs12216809 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXO32 | GRCh38.p7 | 8:123518297 | tacaaagaatatact[C/T]gataaattattattG | 114907 |
rs12335036 | snp | A/C | 0 | 0 | intron-variant | FBXO32 | GRCh38.p7 | 8:123530332 | ACCCTGGCTGAGCCT[A/C]TGCAATCATCTGACT | 114907 |
rs12546268 | snp | C/G | 0.00943375 | 0.0680285 | intron-variant | FBXO32 | GRCh38.p7 | 8:123516812 | GGTTTGTTGCAATTA[C/G]TACTGGTGATCTAGT | 114907 |
rs12678620 | snp | A/T | 0.373196 | 0.217538 | upstream-variant-2KB | FBXO32 | GRCh38.p7 | 8:123543061 | GCCAGAAGGTAGAAG[A/T]TTTGAATTCTAATTC | 114907 |
rs13248667 | snp | A/C | | | intron-variant | FBXO32 | GRCh38.p7 | 8:123521761 | TGACTGGAAAATCTG[A/C]CAGAGTTATCAAAGG | 114907 |
rs13249173 | snp | C/G | 0 | 0 | intron-variant | FBXO32 | GRCh38.p7 | 8:123521760 | CTGACTGGAAAATCT[C/G]CCAGAGTTATCAAAG | 114907 |
rs13251529 | snp | A/G | | | utr-variant-3-prime | FBXO32 | GRCh38.p7 | 8:123501083 | CGACTGCAAACCTGA[A/G]GGCGACGAGGAGTTT | 114907 |
rs13251547 | snp | A/C | | | utr-variant-3-prime | FBXO32 | GRCh38.p7 | 8:123501101 | CGACGAGGAGTTTCT[A/C]CTTTCTTGATCAGCA | 114907 |
rs13251565 | snp | A/G | | | utr-variant-3-prime | FBXO32 | GRCh38.p7 | 8:123501113 | TCTACTTTCTTGATC[A/G]GCATGAAGGGGCAGA | 114907 |
rs13251842 | snp | C/T | | | utr-variant-3-prime | FBXO32 | GRCh38.p7 | 8:123501102 | GACGAGGAGTTTCTA[C/T]TTTCTTGATCAGCAT | 114907 |
rs13252106 | snp | A/G | 0 | 0 | utr-variant-3-prime | FBXO32 | GRCh38.p7 | 8:123501081 | TGCGACTGCAAACCT[A/G]AAGGCGACGAGGAGT | 114907 |
rs13263988 | snp | C/T | 0 | 0 | intron-variant | FBXO32 | GRCh38.p7 | 8:123511284 | gtccccaCTCCACCT[C/T]CACTCCAAGAGGGGT | 114907 |
rs13266414 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | FBXO32 | GRCh38.p7 | 8:123520428 | GCAGTGACGAGCCGT[A/G]CAGTACCAGGAATGG | 114907 |