SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs17645 | snp | C/T | 0.441451 | 0.160769 | missense, upstream-variant-2KB | CD52, UBXN11 | GRCh38.p7 | 1:26320239 | GAAAATGCCTCCGCT[C/T]ATGTTGCTGGATGCT | 91544 |
rs1071849 | snp | A/G | 0.441466 | 0.160751 | missense, upstream-variant-2KB | CD52, UBXN11 | GRCh38.p7 | 1:26320235 | CCTCAGCATCCAGCA[A/G]CATAAGCGGAGGCAT | 91544 |
rs1134580 | snp | C/T | 0.351446 | 0.228492 | synonymous-codon | UBXN11 | GRCh38.p7 | 1:26282392 | CTGTCCCGGTCCCGG[C/T]CCCGGCCCCAGTCCC | 91544 |
rs1134581 | snp | A/G/T | 0 | 0 | missense | UBXN11 | GRCh38.p7 | 1:26282388 | CCCGGTCCCGGTCCC[A/G/T]GCCCCAGTCCCGGTC | 91544 |
rs1134582 | snp | C/T | 0.2262 | 0.248865 | synonymous-codon | UBXN11 | GRCh38.p7 | 1:26282386 | CGGTCCCGGTCCCGG[C/T]CCCAGTCCCGGTCCC | 91544 |
rs1134583 | snp | A/T | 0.2262 | 0.248865 | missense | UBXN11 | GRCh38.p7 | 1:26282382 | CCCGGTCCCGGCCCC[A/T]GTCCCGGTCCCGGTC | 91544 |
rs1134584 | snp | C/T | 0.0425947 | 0.139582 | missense | UBXN11 | GRCh38.p7 | 1:26282337 | GGTCCCGGTCCCGGC[C/T]CCAGTCCCTGTCCCG | 91544 |
rs2276712 | snp | C/T | 0.443102 | 0.158782 | synonymous-codon, intron-variant | UBXN11 | GRCh38.p7 | 1:26300987 | TGAGATCTTTTCTTC[C/T]GAGCCACACCCATCA | 91544 |
rs3732416 | snp | A/G | 0.404035 | 0.196909 | intron-variant | UBXN11 | GRCh38.p7 | 1:26293998 | CTGGCCCACTTCTCC[A/G]CGGTCCTACCTCTGC | 91544 |
rs3795682 | snp | G/T | 0.00478085 | 0.0486577 | utr-variant-5-prime | UBXN11 | GRCh38.p7 | 1:26306662 | AATGAGAAGTGCACG[G/T]GTCCTGGTCGCCTAG | 91544 |
rs3795683 | snp | G/T | 0.490782 | 0.0672626 | intron-variant | UBXN11 | GRCh38.p7 | 1:26306340 | CGTGTCCCCGCCAGA[G/T]CTCTGGGCTCTGGGG | 91544 |
rs3795684 | snp | A/G | 0.490782 | 0.0672626 | intron-variant | UBXN11 | GRCh38.p7 | 1:26306290 | GGTGTGAAGAAGAAT[A/G]TTGTGAGTCAAGCAC | 91544 |
rs3821368 | snp | A/G | 0.404384 | 0.196635 | intron-variant | UBXN11 | GRCh38.p7 | 1:26301310 | TCAGGGTGGCAATGT[A/G]TGGACAGGCCTCCCG | 91544 |
rs3832184 | in-del | -/T | 0.290469 | 0.246703 | intron-variant | UBXN11 | GRCh38.p7 | 1:26294355 | AGCTGACGGTGCCCC[-/T]GCATCTCCCCCTTCT | 91544 |
rs3924324 | snp | A/G | 0.208779 | 0.246578 | intron-variant | UBXN11 | GRCh38.p7 | 1:26289789 | CCTCACTGCACAAGT[A/G]CCCAGGGCACCCCGG | 91544 |
rs3924325 | snp | C/T | 0.183886 | 0.241099 | intron-variant | UBXN11 | GRCh38.p7 | 1:26289829 | CGGTGCCGCCCTCCA[C/T]GTGCCTGCCCTTGAC | 91544 |
rs3924934 | snp | A/G | 0.475348 | 0.108251 | upstream-variant-2KB, intron-variant | CD52, UBXN11 | GRCh38.p7 | 1:26317588 | TTCTGGCTCTTTTTA[A/G]ATTGGTTATTATTAC | 91544 |
rs4233458 | snp | C/T | 0.319376 | 0.240181 | intron-variant | UBXN11 | GRCh38.p7 | 1:26289125 | CCTCAACATGCCCCT[C/T]GCCTTGCGCTCTGGT | 91544 |
rs4233459 | snp | C/T | 0.404035 | 0.196909 | intron-variant | UBXN11 | GRCh38.p7 | 1:26300258 | CGAGGAGCATCTCAT[C/T]GAATCCTCCCAACAC | 91544 |
rs4233460 | snp | A/G | 0.479095 | 0.100076 | upstream-variant-2KB, intron-variant | UBXN11 | GRCh38.p7 | 1:26306896 | GGGATTAGGTTAATG[A/G]AACTGCTGGCAGCCT | 91544 |
rs4290051 | snp | A/G | 0.403334 | 0.197456 | intron-variant | UBXN11 | GRCh38.p7 | 1:26297836 | CCACACCTGGTCCTC[A/G]AACTGGGCAGGTCAG | 91544 |
rs4291487 | snp | A/G | 0.403158 | 0.197592 | intron-variant | UBXN11 | GRCh38.p7 | 1:26300792 | CCAGGTCCCTGCCAC[A/G]ATCAGCCAGGAGTGG | 91544 |
rs4322219 | snp | C/T | 0 | 0 | upstream-variant-2KB, intron-variant | CD52, UBXN11 | GRCh38.p7 | 1:26315960 | ccactgTTTCCTGGC[C/T]ttttttttttttttt | 91544 |
rs4332350 | snp | A/C | 0.285394 | 0.247496 | missense | UBXN11 | GRCh38.p7 | 1:26284400 | AAGGCCTTGTGCATC[A/C]GCTGCCTGCCCACCA | 91544 |
rs4333841 | snp | C/T | 0.49089 | 0.0668743 | intron-variant | UBXN11 | GRCh38.p7 | 1:26305436 | CACAATTTTAGAACA[C/T]TTTCGTCAGCCTAAA | 91544 |
rs4366307 | snp | A/G | 0.487746 | 0.0773096 | upstream-variant-2KB, intron-variant | CD52, UBXN11 | GRCh38.p7 | 1:26317102 | AAAAATTAGCCAGGC[A/G]TGGTGGCACACACCT | 91544 |
rs4370757 | snp | C/T | 0.182614 | 0.240747 | intron-variant | UBXN11 | GRCh38.p7 | 1:26314001 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTTG | 91544 |
rs4450008 | snp | A/C | 0.487684 | 0.0775019 | upstream-variant-2KB, intron-variant | CD52, UBXN11 | GRCh38.p7 | 1:26317369 | ACTGAAACCAGGCTT[A/C]CCGATTCCTCACCTC | 91544 |
rs4471263 | snp | C/T | 0.489665 | 0.0711382 | intron-variant | UBXN11 | GRCh38.p7 | 1:26296209 | GAATGGGTCTGTGAG[C/T]GGGGGAAAGAAAGGT | 91544 |
rs4501829 | snp | C/T | 0.402277 | 0.198272 | intron-variant | UBXN11 | GRCh38.p7 | 1:26315598 | TCTTCTCTCCCTCCC[C/T]GCCCCTCCCTCTCCA | 91544 |
rs4529699 | snp | A/T | 0.404384 | 0.196635 | intron-variant | UBXN11 | GRCh38.p7 | 1:26310039 | ctcaagggatcctcc[A/T]gtctcggcctctcag | 91544 |
rs4625269 | snp | A/C | 0.49089 | 0.0668743 | intron-variant | UBXN11 | GRCh38.p7 | 1:26300476 | CAGACCTGCTAAATC[A/C]CCACTCTGGGAAGCC | 91544 |
rs4639748 | snp | A/G | 0.404035 | 0.196909 | intron-variant | UBXN11 | GRCh38.p7 | 1:26309058 | CAGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 91544 |
rs4659368 | snp | C/T | 0.404035 | 0.196909 | intron-variant | UBXN11 | GRCh38.p7 | 1:26290643 | TGCGGAGTCAGGGGG[C/T]CTCCAACCCAGACTC | 91544 |
rs4659369 | snp | A/G | 0.0763149 | 0.179815 | intron-variant | UBXN11 | GRCh38.p7 | 1:26290848 | GAGATGCAGAGGGTG[A/G]GGGGGAAGGGAGAAC | 91544 |
rs4659370 | snp | C/T | 0.404035 | 0.196909 | intron-variant | UBXN11 | GRCh38.p7 | 1:26293863 | GAACAGAAGGATTGC[C/T]TTTTTTTAAAACGGC | 91544 |
rs4659420 | snp | A/G | 0.474992 | 0.108989 | intron-variant | UBXN11 | GRCh38.p7 | 1:26287842 | AACAACTACCTTAAG[A/G]ACAAATAGGCAAACC | 91544 |
rs4659421 | snp | C/T | 0.402454 | 0.198136 | intron-variant | UBXN11 | GRCh38.p7 | 1:26287976 | GCGGCACAGTCATGA[C/T]ACTGCAACCGTGACC | 91544 |
rs4659422 | snp | A/G | 0.402454 | 0.198136 | intron-variant | UBXN11 | GRCh38.p7 | 1:26288694 | CTTTGAGCCACAGCC[A/G]TCCTTTCTGTGCAAT | 91544 |
rs4659423 | snp | A/C | 0.399968 | 0.200024 | intron-variant | UBXN11 | GRCh38.p7 | 1:26296483 | GGGAAACATTTCAGC[A/C]GAGGGAACAGCAACA | 91544 |
rs4659424 | snp | C/T | 0.399611 | 0.200291 | intron-variant | UBXN11 | GRCh38.p7 | 1:26296502 | GGAACAGCAACAGCA[C/T]GGCCCAAGGCCCTGA | 91544 |
rs4659425 | snp | C/T | 0.404209 | 0.196773 | intron-variant | UBXN11 | GRCh38.p7 | 1:26300237 | CGCTGGCCAGGGGCC[C/T]TCCACCGAGGAGCAT | 91544 |
rs4659426 | snp | C/T | 0.403158 | 0.197592 | upstream-variant-2KB, intron-variant | CD52, UBXN11 | GRCh38.p7 | 1:26317723 | CATGATTCCAGGCCT[C/T]GGGCCCTACTTACTC | 91544 |
rs4659427 | snp | C/T | 0.118235 | 0.212457 | intron-variant, upstream-variant-2KB | CD52, UBXN11 | GRCh38.p7 | 1:26319980 | GAAAAATTAGCCGGG[C/T]GTGGTGGCACGTGCC | 91544 |
rs5773153 | in-del | -/C/CT | 0 | 0 | intron-variant | UBXN11 | GRCh38.p7 | 1:26300636 | AGCTCTACCCTCAGA[-/C/CT]CTTCATCCCTCTCTG | 91544 |
rs5773154 | in-del | -/AA/AAA/AAAA | | | intron-variant | UBXN11 | GRCh38.p7 | 1:26303630 | CGAAACTCCATCTCA[-/AA/AAA/AAAA]AAAAAAAAAAAAAAA | 91544 |
rs5773155 | in-del | -/A | 0.404209 | 0.196773 | intron-variant | UBXN11 | GRCh38.p7 | 1:26305677 | CAATAAAGCTGTCAT[-/A]GGGAAAAAAAAACAA | 91544 |
rs5773156 | snp | C/G/T | 0 | 0 | upstream-variant-2KB, intron-variant | UBXN11 | GRCh38.p7 | 1:26306829 | AGGTCCGGGGCGGGG[C/G/T]GGGGGGGGGGGGTGG | 91544 |
rs5773157 | in-del | -/T/TTGGT | | | upstream-variant-2KB, intron-variant | UBXN11 | GRCh38.p7 | 1:26306837 | GCGGGGTGGGGGGGG[-/T/TTGGT]GGGGTGGTTCGTTCC | 91544 |
rs5773158 | in-del | -/A | 0.400504 | 0.199621 | upstream-variant-2KB, intron-variant | CD52, UBXN11 | GRCh38.p7 | 1:26317082 | AAAAAAAAAAAAAAA[-/A]TACAAAAAATTAGCC | 91544 |
rs6143170 | in-del | -/CAAACTCATTTACGGAATATC | 0.280256 | 0.248162 | upstream-variant-2KB, intron-variant | CD52, UBXN11 | GRCh38.p7 | 1:26317545 | ATCTTCTTTAAACAA[-/CAAACTCATTTACGGAATATC]TGCTATGTTCTGGCT | 91544 |
rs6598952 | snp | G/T | 0.285887 | 0.247418 | intron-variant | UBXN11 | GRCh38.p7 | 1:26282816 | AGAGGCCATCAGCAC[G/T]CGGTGACCCAACGCC | 91544 |
rs6598953 | snp | C/T | 0.402277 | 0.198272 | intron-variant | UBXN11 | GRCh38.p7 | 1:26288122 | GTGTTACCAGGGCTC[C/T]GTCTTCTTTATAGAT | 91544 |
rs6598954 | snp | C/T | 0.401747 | 0.198678 | intron-variant | UBXN11 | GRCh38.p7 | 1:26288360 | AGCTTGCCAAGAAAA[C/T]GGCCCTGGCTTAAAG | 91544 |
rs6598955 | snp | C/T | 0.443866 | 0.157848 | intron-variant | UBXN11 | GRCh38.p7 | 1:26293158 | CGTTTAACTCATTTG[C/T]TCCTTGTAACTCCCA | 91544 |
rs6598956 | snp | A/G | 0.284995 | 0.247539 | intron-variant | UBXN11 | GRCh38.p7 | 1:26296142 | TGGCAGGGCCCATGC[A/G]TGCCTGGGACCCTTC | 91544 |
rs6598957 | snp | C/T | 0.404035 | 0.196909 | upstream-variant-2KB, intron-variant | UBXN11 | GRCh38.p7 | 1:26308409 | agcctcaagagtcca[C/T]gctcttCCTAGAAAC | 91544 |
rs6598958 | snp | A/G | 0.404384 | 0.196635 | intron-variant | UBXN11 | GRCh38.p7 | 1:26310188 | ggtgaatcacctgag[A/G]tcaggagttcgagac | 91544 |
rs6598959 | snp | G/T | 0.28052 | 0.24813 | intron-variant | UBXN11 | GRCh38.p7 | 1:26310280 | cagtggctcatgcct[G/T]taatcccagcacttt | 91544 |
rs6598960 | snp | A/G | 0.404209 | 0.196773 | intron-variant | UBXN11 | GRCh38.p7 | 1:26311376 | tgaactcctgacctc[A/G]tgatccacccgcctc | 91544 |
rs6657644 | snp | C/T | 0.404035 | 0.196909 | intron-variant | UBXN11 | GRCh38.p7 | 1:26291300 | GGGACGCCGGAGAGA[C/T]GTCCCAGGAACAGAA | 91544 |
rs6659387 | snp | A/G | 0.479663 | 0.0987666 | upstream-variant-2KB, intron-variant | UBXN11 | GRCh38.p7 | 1:26307816 | ttttcttgtagagac[A/G]gggtcttgccatgtt | 91544 |
rs6659822 | snp | A/C | 0.248755 | 0.249997 | intron-variant | UBXN11 | GRCh38.p7 | 1:26299917 | ggaggactgattgtg[A/C]ctgggaggctgaggt | 91544 |
rs6665659 | snp | A/G | 0 | 0 | intron-variant | UBXN11 | GRCh38.p7 | 1:26285012 | AACACGAAGCCTCAT[A/G]GGCTCTGGTGGTGGC | 91544 |
rs6666722 | snp | G/T | 0.25634 | 0.24992 | intron-variant | UBXN11 | GRCh38.p7 | 1:26310173 | tgggaggccgaggtg[G/T]gtgaatcacctgaga | 91544 |
rs6667693 | snp | A/C | 0.5 | 0 | missense | UBXN11 | GRCh38.p7 | 1:26282352 | ggccgggaccgggac[A/C]gggactggggccggg | 91544 |
rs6672357 | snp | A/G | 0.375 | 0.216506 | synonymous-codon | UBXN11 | GRCh38.p7 | 1:26282323 | gctgggactgggtcc[A/G]ggacagggactgggg | 91544 |
rs6676527 | snp | C/T | 0.404209 | 0.196773 | upstream-variant-2KB, intron-variant | UBXN11 | GRCh38.p7 | 1:26307507 | ATCATCATCATCTCT[C/T]CACCCTTTCAGCTGT | 91544 |
rs6679251 | snp | C/T | 0.489376 | 0.0721049 | intron-variant | UBXN11 | GRCh38.p7 | 1:26310620 | gtaatcccagctact[C/T]gggaggctaaggcag | 91544 |
rs6681452 | snp | A/G | 0.251578 | 0.249995 | intron-variant | UBXN11 | GRCh38.p7 | 1:26294610 | ATCACTCAGGTCAGC[A/G]CCCAGCCCATGCGAG | 91544 |
rs6686100 | snp | C/G | 0.221439 | 0.248363 | intron-variant | UBXN11 | GRCh38.p7 | 1:26290847 | AGAGATGCAGAGGGT[C/G]GGGGGGAAGGGAGAA | 91544 |
rs6686311 | snp | A/G | 0.40157 | 0.198813 | intron-variant | UBXN11 | GRCh38.p7 | 1:26291087 | AGTCCCAGGCTCCAG[A/G]AAGTTTGATCACCCC | 91544 |
rs6686748 | snp | A/T | 0.28052 | 0.24813 | intron-variant | UBXN11 | GRCh38.p7 | 1:26310398 | caaaaatcagccagg[A/T]gtggtggcatgcgcc | 91544 |
rs6695643 | snp | A/G | 0.401392 | 0.198948 | intron-variant | UBXN11 | GRCh38.p7 | 1:26294507 | TGACCTTGGAAAGCC[A/G]CCTCAGTCCCTAGAG | 91544 |
rs6695966 | snp | C/T | 0.0102149 | 0.0707327 | intron-variant, missense | UBXN11 | GRCh38.p7 | 1:26294270 | GAGACTGTCTTGCTC[C/T]CTGAGTCCTCCTGGT | 91544 |
rs6696025 | snp | C/T | 0.242775 | 0.249896 | intron-variant | UBXN11 | GRCh38.p7 | 1:26291283 | CTGGGGAGAGAGGAA[C/T]GGGGACGCCGGAGAG | 91544 |
rs6696625 | snp | A/G | 0.401392 | 0.198948 | intron-variant, upstream-variant-2KB | CD52, UBXN11 | GRCh38.p7 | 1:26319637 | TGTGAAAGGGGGTGG[A/G]CAGGGGCAGTGATCA | 91544 |
rs6702270 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | UBXN11 | GRCh38.p7 | 1:26295752 | CTCTCTGTACTTGTG[A/T]ACCTGTGTACTCGTT | 91544 |
rs7417118 | snp | A/C | | | intron-variant | UBXN11 | GRCh38.p7 | 1:26293685 | gagccaaatcgtgcc[A/C]ctgcactccagcctg | 91544 |
rs7512569 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | UBXN11 | GRCh38.p7 | 1:26301802 | AAGGCTCTGGGCACC[A/G]GACTTCAGCCAAAGC | 91544 |
rs7513861 | snp | C/T | 0.403509 | 0.197319 | intron-variant | UBXN11 | GRCh38.p7 | 1:26291975 | TATCCCTGACTCCTC[C/T]GGTCCTCTCCCTCAT | 91544 |
rs7517466 | snp | A/G | 0.000167986 | 0.00916323 | intron-variant | UBXN11 | GRCh38.p7 | 1:26284270 | GAGTTGGGAACCGGG[A/G]CCCAGGAAGGACTAT | 91544 |
rs7522068 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | UBXN11 | GRCh38.p7 | 1:26306024 | TACAAGGGCCCCTGA[A/G]GGCAAAGGCTGCATT | 91544 |
rs7522905 | snp | C/T | 0.498504 | 0.0273059 | synonymous-codon | UBXN11 | GRCh38.p7 | 1:26282768 | GAGCGGGGGTGCCGG[C/T]GTGTTGGGTGACTCC | 91544 |
rs7537477 | snp | C/T | 0.491936 | 0.0629843 | intron-variant | UBXN11 | GRCh38.p7 | 1:26292338 | gccttggcaacgtag[C/T]gagacctcgtctcta | 91544 |
rs7541333 | snp | A/G | 0.491368 | 0.0651254 | intron-variant | UBXN11 | GRCh38.p7 | 1:26296398 | GCACTGAGAAAGCTC[A/G]GGATGGAAAACCTGC | 91544 |
rs7541416 | snp | A/G | 0.281841 | 0.247964 | intron-variant | UBXN11 | GRCh38.p7 | 1:26296420 | AAAACCTGCCTAGGA[A/G]GCCCGGGGGATATGA | 91544 |
rs7542844 | snp | A/G | 0.437259 | 0.165632 | intron-variant | UBXN11 | GRCh38.p7 | 1:26291976 | ATCCCTGACTCCTCT[A/G]GTCCTCTCCCTCATG | 91544 |
rs9645430 | snp | A/G | | | intron-variant | UBXN11 | GRCh38.p7 | 1:26298564 | tgggaggccaaggca[A/G]gtggatcacttgagg | 91544 |
rs9645431 | snp | A/T | | | intron-variant | UBXN11 | GRCh38.p7 | 1:26298612 | gcctggccaacatgg[A/T]gaaaccctgcctcta | 91544 |
rs9699419 | snp | C/G | | | upstream-variant-2KB, intron-variant | UBXN11 | GRCh38.p7 | 1:26306831 | GTCCGGGGCGGGGTG[C/G]GGGGGGGGGGTGGTT | 91544 |
rs10159433 | snp | A/G | 0.222035 | 0.248431 | intron-variant | UBXN11 | GRCh38.p7 | 1:26291879 | GCTCCCCTTCCTAGC[A/G]TCATAGGGACTGCAC | 91544 |
rs10794527 | snp | C/T | 0.403684 | 0.197183 | intron-variant | UBXN11 | GRCh38.p7 | 1:26293498 | TTTGGGAGGCCAAGG[C/T]GGGCAGATCACGAGG | 91544 |
rs10902733 | snp | C/T | 0.224709 | 0.248717 | intron-variant | UBXN11 | GRCh38.p7 | 1:26286760 | gctggagtgcaatgg[C/T]acaatcttggatcac | 91544 |
rs10902734 | snp | G/T | 0.473909 | 0.111197 | intron-variant | UBXN11 | GRCh38.p7 | 1:26291432 | CACGGAGGGACCACA[G/T]ATATGGCCAGGGCCT | 91544 |
rs10902735 | snp | C/T | 0.21875 | 0.248039 | intron-variant | UBXN11 | GRCh38.p7 | 1:26291445 | CAGATATGGCCAGGG[C/T]CTCCAAGATGGAGGG | 91544 |
rs10902736 | snp | C/G | 0.40157 | 0.198813 | intron-variant | UBXN11 | GRCh38.p7 | 1:26304270 | GTTTCTTCACCCCCA[C/G]CATCCAGCCTCCCAA | 91544 |
rs10902737 | snp | A/G | 0.479258 | 0.0997024 | intron-variant | UBXN11 | GRCh38.p7 | 1:26309225 | GGCGTGAGCCACTGC[A/G]CCCTGTCCCGAGTCA | 91544 |
rs10902738 | snp | A/G | 0.220544 | 0.248259 | intron-variant | UBXN11 | GRCh38.p7 | 1:26309340 | ccaactctctggttc[A/G]agcaattctcctgcc | 91544 |
rs11247898 | snp | A/G | 0.278791 | 0.248337 | intron-variant | UBXN11 | GRCh38.p7 | 1:26285551 | GCAGCGCTGCAAGGG[A/G]AGAGGAAAAGTGAGG | 91544 |