SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs717739 | snp | G/T | 0 | 0 | intron-variant | FBXO10 | GRCh38.p7 | 9:37543793 | CAAGTAGATGACCTA[G/T]AGCAACTTCCAAGTC | 26267 |
rs927930 | snp | A/G | 0.097727 | 0.198275 | intron-variant | FBXO10 | GRCh38.p7 | 9:37537001 | TTTAAACTTATTCAC[A/G]CACGCTTGACGTCAT | 26267 |
rs1055396 | snp | A/C | | | intron-variant | FBXO10 | GRCh38.p7 | 9:37521376 | GGGTTGCACAGCGGC[A/C]AGGCAGAGGCGCTCC | 26267 |
rs1128206 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | FBXO10 | GRCh38.p7 | 9:37510971 | TGCCGTTACTATTTT[C/T]TAAGAAATGACTTTT | 26267 |
rs1475414 | snp | G/T | 0.474091 | 0.11083 | intron-variant | FBXO10 | GRCh38.p7 | 9:37526451 | TGAGGAATATCATAA[G/T]TAGATCAGTGTTGGG | 26267 |
rs1536551 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | FBXO10 | GRCh38.p7 | 9:37557358 | ACCTCTTTACCCCTT[C/T]GGAGGCCTTGGATGG | 26267 |
rs1571233 | snp | C/G | 0.132066 | 0.220435 | intron-variant | FBXO10 | GRCh38.p7 | 9:37561212 | agaagtgaggtctct[C/G]tgtgttgcccaggct | 26267 |
rs1854159 | snp | C/T | 0.257454 | 0.249889 | intron-variant | FBXO10 | GRCh38.p7 | 9:37564530 | AGGAGGTGGGTTGTA[C/T]CCTGCAAAGCCACAG | 26267 |
rs1854160 | snp | C/T | 0.499396 | 0.0173617 | intron-variant | FBXO10 | GRCh38.p7 | 9:37564702 | GCCCCTTTGGCCAAT[C/T]TCTCCCATTTGGAGT | 26267 |
rs1927153 | snp | C/T | 0.0948562 | 0.196037 | intron-variant | FBXO10 | GRCh38.p7 | 9:37564228 | agtcaagaactgagg[C/T]atagaaacctctact | 26267 |
rs1969936 | snp | C/T | 0.205723 | 0.246048 | intron-variant | FBXO10 | GRCh38.p7 | 9:37561169 | caaaacaaaacaaaa[C/T]CAACttttttttttt | 26267 |
rs1977448 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | FBXO10 | GRCh38.p7 | 9:37523386 | tttttgtattttttt[G/T]tagagacaggatttc | 26267 |
rs2182745 | snp | C/T | 0.200492 | 0.245049 | intron-variant | FBXO10 | GRCh38.p7 | 9:37538450 | aacgtgctggaacta[C/T]gggcgtgagccacca | 26267 |
rs2182746 | snp | A/G | 0.093417 | 0.194889 | intron-variant | FBXO10 | GRCh38.p7 | 9:37531196 | ATAGCCACCATTAAT[A/G]CATAATGCTTATTAT | 26267 |
rs3739572 | snp | A/G | 0.295088 | 0.245901 | intron-variant, downstream-variant-500B | FBXO10 | GRCh38.p7 | 9:37515714 | TCCCCAGGAGGGAAC[A/G]AGCTTTTTAAGAGTC | 26267 |
rs4077401 | snp | C/T | 0.208779 | 0.246578 | intron-variant, upstream-variant-2KB | FBXO10 | GRCh38.p7 | 9:37576103 | CCGCTCAGTCCTGGC[C/T]GAGGCTGAGCGTCTG | 26267 |
rs4242642 | snp | A/G | 0.313814 | 0.241719 | intron-variant | FBXO10 | GRCh38.p7 | 9:37539322 | GCTAAGGTTCTCCTT[A/G]GAAGTCACTGAAAAC | 26267 |
rs4354400 | snp | C/T | 0.0930568 | 0.194599 | intron-variant | FBXO10 | GRCh38.p7 | 9:37530813 | CCCAGCTAATTTTTA[C/T]AATTTTTTGTAGAGA | 26267 |
rs4457420 | snp | A/G | 0.450357 | 0.149522 | intron-variant | FBXO10 | GRCh38.p7 | 9:37513689 | cttcctcccaggttc[A/G]agtgatcctcctggc | 26267 |
rs4581142 | snp | C/T | 0.493568 | 0.0563433 | intron-variant | FBXO10 | GRCh38.p7 | 9:37513746 | agttgcgtgccatga[C/T]gcccagctaattttt | 26267 |
rs4878154 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | FBXO10 | GRCh38.p7 | 9:37515477 | ACGTGAAAGGACAGA[C/G]AGGTTTGAGGAAGAT | 26267 |
rs4878155 | snp | A/G | 0.165853 | 0.235413 | intron-variant, downstream-variant-500B | FBXO10 | GRCh38.p7 | 9:37515535 | GCAGAGTGACTAAAG[A/G]ACAGCAGCAGCATCA | 26267 |
rs4878156 | snp | A/G | 0.16618 | 0.23553 | intron-variant | FBXO10 | GRCh38.p7 | 9:37516854 | taatcccagctactt[A/G]ggaggctgaggcagg | 26267 |
rs4878157 | snp | A/G | 0.499859 | 0.0083854 | intron-variant | FBXO10 | GRCh38.p7 | 9:37517039 | acagaatgaaataac[A/G]gcctttgcagcaatt | 26267 |
rs4878158 | snp | A/G | 0.168135 | 0.236216 | intron-variant | FBXO10 | GRCh38.p7 | 9:37519711 | CTCTGACCTGGGAGG[A/G]GACAGAACTCATTTT | 26267 |
rs4878696 | snp | C/T | 0.124144 | 0.21601 | intron-variant | FBXO10 | GRCh38.p7 | 9:37525384 | AAGTCCACAGGGGCA[C/T]AAAAGCATTTCCTAA | 26267 |
rs4878697 | snp | C/T | 0.496416 | 0.0421803 | intron-variant | FBXO10 | GRCh38.p7 | 9:37549283 | TCCCCTGGGCTCCCA[C/T]AGCACCCAGAGAACA | 26267 |
rs4878698 | snp | A/T | 0.365439 | 0.221752 | intron-variant | FBXO10 | GRCh38.p7 | 9:37551528 | tgcttgtgccctggg[A/T]tctgtagcccagcca | 26267 |
rs4878699 | snp | C/T | 0.234401 | 0.249513 | intron-variant | FBXO10 | GRCh38.p7 | 9:37563808 | tgcaggagatcattt[C/T]ggaattttaaggttt | 26267 |
rs4878700 | snp | G/T | 0.133435 | 0.221162 | intron-variant | FBXO10 | GRCh38.p7 | 9:37564549 | gcaaagccacagggg[G/T]ggagctgcccaaggc | 26267 |
rs5897689 | in-del | -/AC | 0.00517822 | 0.0506191 | intron-variant | FBXO10 | GRCh38.p7 | 9:37523222 | CCCGGCACCTACTAT[-/AC]ACCCAATGGCCTTGA | 26267 |
rs6476636 | snp | A/G | 0.496616 | 0.0409947 | intron-variant | FBXO10 | GRCh38.p7 | 9:37514783 | AGGTTGCAGTGAGCC[A/G]AGATCGCACCACTGC | 26267 |
rs6476637 | snp | C/T | 0.197703 | 0.244469 | intron-variant | FBXO10 | GRCh38.p7 | 9:37534478 | AAAAAGAAAGACAGG[C/T]GCCTCCAAGGAGACG | 26267 |
rs6476638 | snp | A/G | 0.242201 | 0.249878 | intron-variant | FBXO10 | GRCh38.p7 | 9:37554888 | gctattatggataat[A/G]ctgctgtgaatattc | 26267 |
rs6476639 | snp | A/T | 0.24449 | 0.249939 | intron-variant | FBXO10 | GRCh38.p7 | 9:37558310 | GCTAATGGTTGGTAT[A/T]CCAAGTCTCAGGAGG | 26267 |
rs6476640 | snp | C/G | 0.498632 | 0.0261223 | intron-variant | FBXO10 | GRCh38.p7 | 9:37558488 | GCACTGACAATTTCT[C/G]TCCCAGATGGGTTTC | 26267 |
rs6476643 | snp | G/T | 0.279991 | 0.248195 | upstream-variant-2KB, utr-variant-5-prime | FBXO10 | GRCh38.p7 | 9:37576451 | CCCGACCACCGCGCA[G/T]AAAAGCTGTATCTGC | 26267 |
rs7018980 | snp | G/T | 0.499017 | 0.0221427 | intron-variant | FBXO10 | GRCh38.p7 | 9:37570224 | GCTGAGGAGGCAGGA[G/T]AATCCCTTGAACCCG | 26267 |
rs7020950 | snp | A/G | 0.128288 | 0.218372 | intron-variant | FBXO10 | GRCh38.p7 | 9:37514578 | cggtggctcacacct[A/G]taatctcaatacttt | 26267 |
rs7023107 | snp | C/T | 0.499846 | 0.00878459 | intron-variant | FBXO10 | GRCh38.p7 | 9:37550161 | gttttcTTTTTTTGT[C/T]GTCTCAGGTtttttt | 26267 |
rs7024249 | snp | A/G | 0.00472811 | 0.0483911 | intron-variant | FBXO10 | GRCh38.p7 | 9:37520727 | tttctgcctctctaa[A/G]aaggaaaactcactg | 26267 |
rs7027678 | snp | C/T | 0.356811 | 0.226034 | intron-variant | FBXO10 | GRCh38.p7 | 9:37528459 | TTTGCTCATGCTGTT[C/T]CATTACTAGGAACAT | 26267 |
rs7027892 | snp | A/G | 0.356811 | 0.226034 | intron-variant | FBXO10 | GRCh38.p7 | 9:37528407 | CAAGCCACCGTCAAC[A/G]GTTTGCTAACCCCTG | 26267 |
rs7028288 | snp | C/G | 0 | 0 | missense, downstream-variant-500B, nc-transcript-variant | FBXO10 | GRCh38.p7 | 9:37521654 | CTTCTCCAGCTCTGT[C/G]TCCCAGAGGATGGCG | 26267 |
rs7031794 | snp | C/T | 0.499053 | 0.0217445 | intron-variant | FBXO10 | GRCh38.p7 | 9:37552095 | acctcatcagactag[C/T]cttcactgttgcaac | 26267 |
rs7035751 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | FBXO10 | GRCh38.p7 | 9:37535832 | CTGGGCCTTCACACA[C/T]ACCTCCTTTGCCTCG | 26267 |
rs7037295 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | FBXO10 | GRCh38.p7 | 9:37523848 | cttgaacctgggagg[C/T]ggaggttgcagtgag | 26267 |
rs7037435 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | FBXO10 | GRCh38.p7 | 9:37524001 | AAGCCTGTGAGAAGG[C/T]GCTAGCCTCACCTGC | 26267 |
rs7039920 | snp | C/T | 0.499203 | 0.0199521 | intron-variant | FBXO10 | GRCh38.p7 | 9:37557723 | TACTATGTCCCCACA[C/T]GGTTTACATTTATCT | 26267 |
rs7041752 | snp | A/G | 0.497855 | 0.0326773 | intron-variant | FBXO10 | GRCh38.p7 | 9:37524778 | GGGCGGAGGTTTCCA[A/G]AGCAGGCAGAGGTCC | 26267 |
rs7043428 | snp | A/C | 0.0345262 | 0.126772 | intron-variant | FBXO10 | GRCh38.p7 | 9:37567218 | tgtgatcttggctca[A/C]tacagcctcaatctc | 26267 |
rs7044153 | snp | A/G | 0.472309 | 0.114363 | synonymous-codon, nc-transcript-variant | FBXO10 | GRCh38.p7 | 9:37537560 | CTTTGGGGAGCTAGA[A/G]GCTGGGCTGGTAGGG | 26267 |
rs7044233 | snp | C/T | 0.498611 | 0.0263212 | intron-variant | FBXO10 | GRCh38.p7 | 9:37560610 | ATGAAACAACAGGGA[C/T]TTCTTAGAACAAGGT | 26267 |
rs7044561 | snp | G/T | 0.00843964 | 0.0644096 | missense, nc-transcript-variant | FBXO10 | GRCh38.p7 | 9:37537895 | CATGGACCTGGATGT[G/T]CCCGTTCTCAAAGTT | 26267 |
rs7048273 | snp | A/G | 0.494976 | 0.0498674 | intron-variant | FBXO10 | GRCh38.p7 | 9:37538388 | AGGTATACTGCCATT[A/G]CCAGGAAGCATTGAA | 26267 |
rs7048462 | snp | A/G | 0.161267 | 0.233723 | intron-variant | FBXO10 | GRCh38.p7 | 9:37538751 | cgggggttgactgca[A/G]gtgttatcttggaca | 26267 |
rs7341712 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | FBXO10 | GRCh38.p7 | 9:37553973 | agatcctttgcttgg[C/T]ttaccccaatggtaa | 26267 |
rs7341863 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | FBXO10 | GRCh38.p7 | 9:37554091 | tgtactcacttgtgt[A/G]tgtgtattaagttct | 26267 |
rs7850177 | snp | C/T | 0.498611 | 0.0263212 | intron-variant | FBXO10 | GRCh38.p7 | 9:37562519 | GGAATTAAATGTTTT[C/T]CTTCATTTATTGTCT | 26267 |
rs7851820 | snp | A/G | 0 | 0 | intron-variant | FBXO10 | GRCh38.p7 | 9:37550762 | gcgattataggcacc[A/G]cacccagccTATTTC | 26267 |
rs7851984 | snp | A/G | 0 | 0 | intron-variant | FBXO10 | GRCh38.p7 | 9:37520548 | ttttttttttttgta[A/G]aaaccaagtcttgtt | 26267 |
rs7852508 | snp | C/T | 0.046775 | 0.145601 | intron-variant | FBXO10 | GRCh38.p7 | 9:37515117 | GACAGGTGACATTGG[C/T]GGTGCAGGAGTGATA | 26267 |
rs7855367 | snp | C/T | 0.167158 | 0.235875 | intron-variant | FBXO10 | GRCh38.p7 | 9:37519155 | ACCTCGTGATCCACC[C/T]GCCTCGGCCTCCCAA | 26267 |
rs7855746 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | FBXO10 | GRCh38.p7 | 9:37551452 | gaggcacacaagcct[C/T]cacagctcttgtact | 26267 |
rs7865784 | snp | A/G | 0.161267 | 0.233723 | intron-variant | FBXO10 | GRCh38.p7 | 9:37518987 | CCATCTCGGCTCACT[A/G]CAAGCTCCGCCTCCC | 26267 |
rs7865834 | snp | A/G | 0.340559 | 0.233022 | intron-variant | FBXO10 | GRCh38.p7 | 9:37518764 | CGCCATCCTACTGCC[A/G]CTTACACCTCCCTGA | 26267 |
rs7865842 | snp | A/G | 0.0733688 | 0.176922 | intron-variant | FBXO10 | GRCh38.p7 | 9:37518778 | CGCTTACACCTCCCT[A/G]ACGGGGTGCTCACTG | 26267 |
rs7866748 | snp | A/G | 0.47743 | 0.103805 | intron-variant | FBXO10 | GRCh38.p7 | 9:37566459 | TGAGACTCTGTCTCG[A/G]AAAAAAAAAAAAAAA | 26267 |
rs7868084 | snp | C/T | | | intron-variant | FBXO10 | GRCh38.p7 | 9:37545314 | cctgagtagctggga[C/T]tacaggcgcacaccg | 26267 |
rs7868924 | snp | A/G | 0.167484 | 0.23599 | intron-variant | FBXO10 | GRCh38.p7 | 9:37519185 | AAGTGCTGGGATTAC[A/G]GGCGTGAGCCACCAT | 26267 |
rs7873615 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | FBXO10 | GRCh38.p7 | 9:37543275 | AGGTAAGGTTCCCAG[C/T]AGATGTATATGTAGA | 26267 |
rs9775795 | snp | C/G | | | intron-variant, upstream-variant-2KB | FBXO10 | GRCh38.p7 | 9:37533456 | gaggctaaggcagga[C/G]aatctcttgaatcag | 26267 |
rs9969717 | snp | C/T | 0.215747 | 0.247642 | intron-variant, upstream-variant-2KB | FBXO10 | GRCh38.p7 | 9:37532401 | CGCCTCCCAGGCTCA[C/T]GTGATCCTCCCACCT | 26267 |
rs10114827 | snp | C/T | 0.12932 | 0.218944 | intron-variant, downstream-variant-500B | FBXO10 | GRCh38.p7 | 9:37515442 | acactgagtggatgg[C/T]gatgtcgctgaaatg | 26267 |
rs10116329 | snp | C/T | 0.0912534 | 0.193131 | intron-variant | FBXO10 | GRCh38.p7 | 9:37561993 | agtctaacatctcaa[C/T]ggcatgacatggaaa | 26267 |
rs10116373 | snp | C/T | 0.180064 | 0.240019 | intron-variant | FBXO10 | GRCh38.p7 | 9:37526056 | CCTCCAGAAAGGATC[C/T]GTGGCCACCTGGAGA | 26267 |
rs10117312 | snp | A/G | 0.498774 | 0.02473 | intron-variant | FBXO10 | GRCh38.p7 | 9:37557384 | GATGGCTCTGCCTCT[A/G]ATTATTCTTTTCTTA | 26267 |
rs10117614 | snp | A/G | 0.12932 | 0.218944 | intron-variant, downstream-variant-500B | FBXO10 | GRCh38.p7 | 9:37515459 | atgtcgctgaaatgg[A/G]gaacgtgaaaggaca | 26267 |
rs10118103 | snp | A/G | 0.499424 | 0.0169631 | intron-variant | FBXO10 | GRCh38.p7 | 9:37563939 | TCACCAAGATAATGT[A/G]GAAAATGTCTGCAGG | 26267 |
rs10118277 | snp | A/C | 0.437683 | 0.165152 | intron-variant | FBXO10 | GRCh38.p7 | 9:37558783 | AATTAAGCACTACTG[A/C]AGCTTATAGAGATCA | 26267 |
rs10119802 | snp | C/G | 0.0926964 | 0.194308 | intron-variant | FBXO10 | GRCh38.p7 | 9:37565941 | CTTAGGACATGTTGG[C/G]AGGTTCAGTCTGGCT | 26267 |
rs10121333 | snp | C/T | 0.499477 | 0.0161657 | intron-variant | FBXO10 | GRCh38.p7 | 9:37563938 | ATCACCAAGATAATG[C/T]GGAAAATGTCTGCAG | 26267 |
rs10121547 | snp | A/G | 0.0916144 | 0.193427 | intron-variant | FBXO10 | GRCh38.p7 | 9:37567777 | tcaggtgatctgtcc[A/G]cctcggcctcccaaa | 26267 |
rs10122666 | snp | A/G | 0.499017 | 0.0221427 | intron-variant | FBXO10 | GRCh38.p7 | 9:37556841 | TGAGCCACCGCATCC[A/G]GCCTGTTCTGTATTC | 26267 |
rs10122829 | snp | C/T | 0.0711525 | 0.174681 | intron-variant | FBXO10 | GRCh38.p7 | 9:37540922 | CTCCAGTTGGTCCAG[C/T]TGGAAAGGGAAGAGG | 26267 |
rs10123823 | snp | G/T | 0.12932 | 0.218944 | intron-variant, downstream-variant-500B | FBXO10 | GRCh38.p7 | 9:37515495 | gtttgaggaagaTGG[G/T]TGGCGGCAATTGTGA | 26267 |
rs10124667 | snp | C/T | 0.125182 | 0.216612 | intron-variant | FBXO10 | GRCh38.p7 | 9:37516503 | AAAGTCACTAACCCA[C/T]GAAGCTGCAGAACTG | 26267 |
rs10124731 | snp | C/T | 0.125182 | 0.216612 | intron-variant | FBXO10 | GRCh38.p7 | 9:37516745 | ctgaggcaggtggat[C/T]gatcacctgaggtca | 26267 |
rs10124736 | snp | C/T | 0.125182 | 0.216612 | intron-variant | FBXO10 | GRCh38.p7 | 9:37516773 | tcaggagtttgagac[C/T]agcctgaccaacatg | 26267 |
rs10125441 | snp | C/T | 0.228842 | 0.249103 | intron-variant | FBXO10 | GRCh38.p7 | 9:37547259 | ATACAAAGGGATAAA[C/T]CATTGATGTAGACAA | 26267 |
rs10217806 | snp | C/T | 0.178465 | 0.239547 | intron-variant | FBXO10 | GRCh38.p7 | 9:37544182 | gctgagacaggagaa[C/T]tgcttgaacctggga | 26267 |
rs10570076 | in-del | -/GA | 0.19646 | 0.2442 | intron-variant | FBXO10 | GRCh38.p7 | 9:37534688 | AAACTGGGGGCAGAT[-/GA]GAGACTGGAGACAGC | 26267 |
rs10696134 | in-del | -/T | | | intron-variant | FBXO10 | GRCh38.p7 | 9:37561194 | TTTTTTTTTTTTTTT[-/T]AAAGAAGTGAGGTCT | 26267 |
rs10701235 | in-del | -/AT/ATTTT | | | intron-variant | FBXO10 | GRCh38.p7 | 9:37560645 | TTTTTATTTTATTTT[-/AT/ATTTT]TTTTAATGCATTCAA | 26267 |
rs10733488 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FBXO10 | GRCh38.p7 | 9:37517684 | GACTGCAGTGCAAGG[C/G]GGGCAGGAGGTATGC | 26267 |
rs10758436 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXO10 | GRCh38.p7 | 9:37517494 | GGGAGACAAATAGGT[A/G]AAGGAAGAGATACCA | 26267 |
rs10758437 | snp | C/T | 0.496681 | 0.0405994 | intron-variant | FBXO10 | GRCh38.p7 | 9:37520443 | gggctcaagcgatcc[C/T]cccgcctcctgagta | 26267 |
rs10758438 | snp | C/T | 0.498832 | 0.0241331 | intron-variant | FBXO10 | GRCh38.p7 | 9:37550639 | cctgcaccacacacc[C/T]ggctaatttttgtag | 26267 |
rs10758439 | snp | A/G | 0.498632 | 0.0261223 | intron-variant | FBXO10 | GRCh38.p7 | 9:37559728 | TTCATTGCCTATGCA[A/G]GATCATCCACAGCTT | 26267 |
rs10758440 | snp | A/C | 0.272511 | 0.248984 | intron-variant | FBXO10 | GRCh38.p7 | 9:37573333 | AACCCAGCCTGGTGA[A/C]AAGCTCAACAAAAGC | 26267 |