SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs15036 | snp | A/C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779661 | GTACACATTGCAGAT[A/C/G]AAATATTTGGAGTTA | 9100 |
rs173419 | snp | A/C | 0.24019 | 0.249807 | intron-variant | USP10 | GRCh38.p7 | 16:84773925 | CTGTATTTTTATATC[A/C]GCTGCCACCTCCAAT | 9100 |
rs244562 | snp | C/T | 0.340333 | 0.233109 | intron-variant | USP10 | GRCh38.p7 | 16:84773655 | CACACTTCTAGCTGC[C/T]TTATCACTCATCAGC | 9100 |
rs244563 | snp | A/G | 0.264084 | 0.249603 | intron-variant | USP10 | GRCh38.p7 | 16:84773352 | TGGGAAGCAGAAAAG[A/G]GGACACTGGGCCTCA | 9100 |
rs244564 | snp | A/G | 0.250168 | 0.25 | intron-variant | USP10 | GRCh38.p7 | 16:84772178 | tgcctctgccaccca[A/G]gtagctggggttaca | 9100 |
rs744838 | snp | A/G | 0.499984 | 0.00279548 | intron-variant | USP10 | GRCh38.p7 | 16:84741080 | AGGAAACTGATGCCA[A/G]ACTTTTTCTTTGAGA | 9100 |
rs744839 | snp | C/T | 0.499502 | 0.0157669 | intron-variant | USP10 | GRCh38.p7 | 16:84740830 | TGACTCTTGGGAACT[C/T]AGGTCAACTCTTCAC | 9100 |
rs774294 | snp | A/G | 0.485664 | 0.0834419 | intron-variant | USP10 | GRCh38.p7 | 16:84769017 | GATGTGCCAGCTTAT[A/G]GCTATTTTGTACTCT | 9100 |
rs774295 | snp | A/C | 0.484701 | 0.0861117 | intron-variant | USP10 | GRCh38.p7 | 16:84769085 | TGTGGCAGTGAATTC[A/C]TAAAAATGCACTGGG | 9100 |
rs774296 | snp | A/G | 0.376592 | 0.215579 | intron-variant | USP10 | GRCh38.p7 | 16:84769282 | GTGTGCTCTGAGTCA[A/G]AAAGAGCAAAGTAGG | 9100 |
rs774297 | snp | C/G | 0.380919 | 0.21298 | intron-variant | USP10 | GRCh38.p7 | 16:84770803 | AAATCTCCAGTGGCT[C/G]ATGCCTGTAATCCCA | 9100 |
rs774298 | snp | C/G | 0.502104 | 0.0366843 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84775218 | CCGAACCTATCGGCT[C/G]TTTGCAGGTGAGTAA | 9100 |
rs774299 | snp | A/G | 0.46885 | 0.12085 | intron-variant | USP10 | GRCh38.p7 | 16:84775294 | TACAGCTGGGCACAG[A/G]TTTGCTGCAACTTAG | 9100 |
rs774300 | snp | C/T | 0.361053 | 0.22398 | intron-variant | USP10 | GRCh38.p7 | 16:84775378 | GTCACGTGAGAGTTT[C/T]ACCTGAAACTCTGCG | 9100 |
rs774301 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84776465 | ACTTGCTGGGCCTCA[C/G]ATGGGACGGCCATGG | 9100 |
rs774302 | snp | C/T | 0.326741 | 0.23793 | intron-variant | USP10 | GRCh38.p7 | 16:84776618 | GGCCAGCAGTTTCTC[C/T]GCCTTCTCCCTGCAC | 9100 |
rs774303 | snp | A/G | 0.102014 | 0.201495 | intron-variant | USP10 | GRCh38.p7 | 16:84777083 | TTAGAATTACCTGTA[A/G]AGTGAGCAAAGGAAC | 9100 |
rs774304 | snp | A/G | 0.428937 | 0.17459 | intron-variant | USP10 | GRCh38.p7 | 16:84777343 | CCCCCAGGCCCTGCA[A/G]ATTCTACTGATGGTC | 9100 |
rs774305 | snp | C/G | 0.187685 | 0.242109 | intron-variant | USP10 | GRCh38.p7 | 16:84777997 | ATGTGTTCTGTGGCT[C/G]TCTTAATGTTTTCAT | 9100 |
rs774306 | snp | A/G | 0.349233 | 0.229462 | intron-variant | USP10 | GRCh38.p7 | 16:84778355 | TAATATACCATAAGC[A/G]TATTCCCGCATCACC | 9100 |
rs774307 | snp | A/G | 0.476746 | 0.10529 | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780193 | AGCCCACCGTTTTCA[A/G]TATCACCAAAATAGT | 9100 |
rs774308 | snp | C/T | 0.0648419 | 0.167978 | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780359 | AGGGTGCCCGTGCCC[C/T]GGCTTCTGGCCCTGT | 9100 |
rs811330 | snp | A/C | 0.462363 | 0.131916 | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780102 | TTAGTGATTTGGGTA[A/C]ACGAAGTTTTTGACT | 9100 |
rs958309 | snp | A/G | 0.287606 | 0.247155 | intron-variant | USP10 | GRCh38.p7 | 16:84733364 | CAGAAAAAATGCTAC[A/G]TATTTTAACAATCCT | 9100 |
rs958310 | snp | A/G | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84733285 | AGGATCTGCAACTCA[A/G]AGTTCTAGGTTGTTT | 9100 |
rs958311 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84733147 | GTCCTGCTTGCAGGA[A/G]ATTTTTATTGGTTCA | 9100 |
rs963246 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | USP10 | GRCh38.p7 | 16:84754999 | AAACACAGCTCCTTT[G/T]TTTTTTTTTCTGGGA | 9100 |
rs964453 | snp | A/G | 0.379942 | 0.213577 | intron-variant | USP10 | GRCh38.p7 | 16:84734629 | ttgacattaaagttg[A/G]aagtgtactcctctt | 9100 |
rs1050423 | snp | G/T | 0 | 0 | utr-variant-5-prime, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84700063 | TGAGCAGCCGGAGGA[G/T]CGCGGAGTCCCAATG | 9100 |
rs1050424 | snp | C/G | | | utr-variant-5-prime, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84700067 | CAGCCGGAGGATCGC[C/G]GAGTCCCAATGAAAC | 9100 |
rs1050435 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745500 | CTGTCAGCCAGCCCA[A/G]GTCCTGGGCCAGCCT | 9100 |
rs1477392 | snp | C/T | 0.496517 | 0.0415876 | intron-variant | USP10 | GRCh38.p7 | 16:84755342 | CCCACCCAGAAACTT[C/T]GCTGCATCTTCCTGG | 9100 |
rs1541696 | snp | C/T | 0.482534 | 0.0918038 | intron-variant | USP10 | GRCh38.p7 | 16:84761238 | TCCACCTGTGCTAGG[C/T]GGGCCCCTCTGGGTT | 9100 |
rs1541697 | snp | C/T | 0.288386 | 0.247035 | intron-variant | USP10 | GRCh38.p7 | 16:84761030 | CTTAAGACCCTATGC[C/T]ACCCCTGGTGGTATC | 9100 |
rs1541698 | snp | C/T | 0.481242 | 0.0950111 | intron-variant | USP10 | GRCh38.p7 | 16:84761026 | AGACCCTATGCTACC[C/T]CTGGTGGTATCCTGC | 9100 |
rs1541699 | snp | A/G | 0.308166 | 0.243139 | intron-variant | USP10 | GRCh38.p7 | 16:84714290 | TTTTACTAAACAAGT[A/G]TCATTCCACATTTTA | 9100 |
rs1812061 | snp | C/G | 0.326436 | 0.238028 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745091 | AAGTCCTGGGCGTAA[C/G]TGACGGGGGCATGTC | 9100 |
rs1812062 | snp | A/G | 0.326247 | 0.238089 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745084 | GGGCGTAACTGACGG[A/G]GGCATGTCACCCATA | 9100 |
rs1820246 | snp | C/T | 0.28052 | 0.24813 | intron-variant | USP10 | GRCh38.p7 | 16:84725628 | agtctgttctctgac[C/T]cctgacctcaggtga | 9100 |
rs1862792 | snp | A/G | 0.354634 | 0.22705 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745079 | GAATTTATGGGTGAC[A/G]TGCCCCCGTCAGTTA | 9100 |
rs1862794 | snp | C/T | 0.370162 | 0.219229 | intron-variant | USP10 | GRCh38.p7 | 16:84716989 | TTCATAGTAGAGCTT[C/T]GGGATTACATGAGAT | 9100 |
rs1968266 | snp | C/T | 0.278399 | 0.248382 | intron-variant | USP10 | GRCh38.p7 | 16:84705606 | CCTCTTTCTTTCTTC[C/T]TGATCTGATGGTGCT | 9100 |
rs2012708 | snp | C/T | 0.495213 | 0.048687 | intron-variant | USP10 | GRCh38.p7 | 16:84756953 | GAGCCCTTTCCTCAA[C/T]ATATAAGGGGCTTCA | 9100 |
rs2012733 | snp | A/C | 0.284995 | 0.247539 | intron-variant | USP10 | GRCh38.p7 | 16:84757222 | CTTAATATGGAATAC[A/C]GAACTGGGCCTTGAA | 9100 |
rs2113253 | snp | C/T | 0.278399 | 0.248382 | intron-variant | USP10 | GRCh38.p7 | 16:84707994 | gaggtgggaggatcg[C/T]ttgaacctgggaggt | 9100 |
rs2161692 | snp | C/T | 0.301681 | 0.2446 | intron-variant | USP10 | GRCh38.p7 | 16:84736881 | GCAAGCTCCGCCTCC[C/T]GGGTTCACACCATTC | 9100 |
rs2216762 | snp | C/T | 0.422315 | 0.181128 | intron-variant | USP10 | GRCh38.p7 | 16:84725840 | TTAAGGCTTTAATCA[C/T]GCCAAACAGTCTATT | 9100 |
rs2288017 | snp | C/G | 0.131898 | 0.220361 | intron-variant | USP10 | GRCh38.p7 | 16:84760143 | AGTTCATTGTAGTTA[C/G]GAAAACCTGTGTCCT | 9100 |
rs2291648 | snp | C/T | 0.49263 | 0.0602539 | intron-variant | USP10 | GRCh38.p7 | 16:84766879 | CTTTATTCACACCAA[C/T]TGAAAGATTTACTTC | 9100 |
rs2291649 | snp | A/G | 0.373397 | 0.217424 | intron-variant | USP10 | GRCh38.p7 | 16:84767301 | AATGAGAGATGGGCC[A/G]AACACACAATTTTTA | 9100 |
rs2303231 | snp | G/T | 0.227959 | 0.249026 | intron-variant | USP10 | GRCh38.p7 | 16:84775016 | ATGAGTCAATTTTTG[G/T]GCAACTGAAGGGATA | 9100 |
rs2303232 | snp | C/G | 0.307176 | 0.243374 | intron-variant | USP10 | GRCh38.p7 | 16:84775363 | CTTGTGAGTCGGGGA[C/G]TCACGTGAGAGTTTT | 9100 |
rs2326391 | snp | C/T | 0.326376 | 0.238048 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745088 | GGTGACATGCCCCCG[C/T]CAGTTACGCCCAGGA | 9100 |
rs2326392 | snp | C/G | 0.416708 | 0.186302 | intron-variant | USP10 | GRCh38.p7 | 16:84747182 | TGGATTCCACCAAGC[C/G]TGGTGACCAGATCTT | 9100 |
rs2550409 | snp | C/T | 0.379158 | 0.214052 | | | GRCh38.p7 | 16:84767876 | GGGAAGGTCAGCAGA[C/T]AAACAAGTGAACAAA | 9100 |
rs2641688 | snp | A/G | 0.361667 | 0.223675 | intron-variant | USP10 | GRCh38.p7 | 16:84768145 | ATCTTAAGGGAAAGT[A/G]GCAAGGAGTGGTCTC | 9100 |
rs2641694 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84770168 | GGACTCCGGAAGATA[A/T]AAAGGATGCTGCCAG | 9100 |
rs2641695 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84766518 | GTTTAGGATTGTGAG[A/G]ACACCCCCTCGGGAT | 9100 |
rs3180185 | snp | A/G | 0.277067 | 0.24853 | intron-variant | USP10 | GRCh38.p7 | 16:84755657 | AATAATTATGATTGG[A/G]TATGGTGGCACACAT | 9100 |
rs3213810 | snp | A/T | 0.419616 | 0.183658 | intron-variant | USP10 | GRCh38.p7 | 16:84764031 | GATCTGTGCCTTTTT[A/T]TTTTTTGCTGTTCTT | 9100 |
rs3751759 | snp | C/T | 0.411282 | 0.191019 | intron-variant | USP10 | GRCh38.p7 | 16:84744616 | TGTTTAGAAAGAAAA[C/T]TATTAGTTAAGAACC | 9100 |
rs3751760 | snp | C/G | 0.322245 | 0.239334 | intron-variant | USP10 | GRCh38.p7 | 16:84744443 | ATTATTTAATTTGGG[C/G]ATATGAAAAGCAGAA | 9100 |
rs3751761 | snp | C/G | 0.252702 | 0.249985 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699945 | GGGCGCGGGGAGGCC[C/G]GCCCGCTGCTGCGCC | 9100 |
rs3751866 | snp | A/G | 0.412082 | 0.190341 | intron-variant | USP10 | GRCh38.p7 | 16:84737698 | GGTGACAGTGCCAGC[A/G]GGTGACACTGCCAGT | 9100 |
rs3764281 | snp | C/T | 0.322858 | 0.239148 | intron-variant | USP10 | GRCh38.p7 | 16:84733546 | AAACATAACTATTAA[C/T]TGTATCTACCCACGG | 9100 |
rs3764283 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | USP10 | GRCh38.p7 | 16:84733234 | AACCTTTCCTACAAA[C/T]TGTCAAAGAACACTA | 9100 |
rs3764284 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | USP10 | GRCh38.p7 | 16:84708075 | CTTTTCTTTTTTGAC[A/G]TAAGAGTCTCGCTCT | 9100 |
rs3764286 | snp | A/G | 0.412416 | 0.190055 | intron-variant | USP10 | GRCh38.p7 | 16:84707737 | ATGTTATAAGTTGTG[A/G]CAGCACTTCCACAAT | 9100 |
rs3764331 | snp | C/T | 0.40853 | 0.193309 | intron-variant | USP10 | GRCh38.p7 | 16:84759742 | AGTGAACTCAAGTCT[C/T]TTCTATATGCATTTT | 9100 |
rs3764332 | snp | A/T | 0.231775 | 0.249335 | intron-variant | USP10 | GRCh38.p7 | 16:84759679 | GCTAAAATATTTTCT[A/T]CTGAATCTAAAGAAC | 9100 |
rs3764333 | snp | C/T | 0.361053 | 0.22398 | intron-variant | USP10 | GRCh38.p7 | 16:84759655 | AAAGAACACAGATCA[C/T]CAATGCTCCAATTCC | 9100 |
rs3829516 | snp | A/G | 0.412082 | 0.190341 | intron-variant | USP10 | GRCh38.p7 | 16:84744320 | TAAAAATACCCCCCA[A/G]TGGAATCTGACTTTC | 9100 |
rs3829554 | snp | A/G | 0.499999 | 0.000798721 | intron-variant | USP10 | GRCh38.p7 | 16:84737437 | GTCTGTGGTAACTGG[A/G]TATCTAAATACACAA | 9100 |
rs3893782 | snp | A/C | 0.479824 | 0.098392 | intron-variant | USP10 | GRCh38.p7 | 16:84773231 | AGCACAGCTTCAAGA[A/C]GACTTTTCTTGAAAG | 9100 |
rs4510001 | snp | A/G | 0.287346 | 0.247195 | intron-variant | USP10 | GRCh38.p7 | 16:84740514 | TCAAAGTGATTCAGC[A/G]ATTAAATACATTACA | 9100 |
rs4553618 | snp | A/G | 0.370457 | 0.219066 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745156 | TCCGGGGAAAGGACT[A/G]TCAGGCACAATGTCA | 9100 |
rs4782652 | snp | C/G | 0.292008 | 0.246445 | intron-variant | USP10 | GRCh38.p7 | 16:84738159 | TCCCAGCCTGCTGCA[C/G]TCTCTCGGGTCTGGA | 9100 |
rs4782653 | snp | C/T | 0.300169 | 0.244914 | intron-variant | USP10 | GRCh38.p7 | 16:84746794 | gaaattaaccttaac[C/T]tactgtaactttttt | 9100 |
rs4782654 | snp | A/G | 0.245916 | 0.249967 | intron-variant | USP10 | GRCh38.p7 | 16:84755444 | GCTGTCTTCACTCCT[A/G]CACGCTGCCCCCACT | 9100 |
rs4782655 | snp | C/G | 0.287606 | 0.247155 | intron-variant | USP10 | GRCh38.p7 | 16:84763593 | TGACACGGTAATACC[C/G]ACTTTGCAGAGCATC | 9100 |
rs4782656 | snp | G/T | 0.420574 | 0.182769 | intron-variant | USP10 | GRCh38.p7 | 16:84765028 | tgcagtgagccaaga[G/T]tacaccactgcactc | 9100 |
rs4783053 | snp | C/T | 0.283158 | 0.247791 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699591 | ATAAACCAGACCCTC[C/T]TCGGGGATCTAATGC | 9100 |
rs4783054 | snp | A/G | 0.456214 | 0.141336 | intron-variant | USP10 | GRCh38.p7 | 16:84701475 | TGTTTAGACCTTTCT[A/G]TTAAAAAAAAAGATT | 9100 |
rs4783055 | snp | A/C | 0.389715 | 0.207315 | intron-variant | USP10 | GRCh38.p7 | 16:84708597 | AAACTGGGTAATTCA[A/C]CTGAATTTTTCTCCA | 9100 |
rs4783056 | snp | A/G | 0.303938 | 0.244112 | intron-variant | USP10 | GRCh38.p7 | 16:84748526 | ccaggctggtcttga[A/G]ctcctgacctcaagt | 9100 |
rs4783057 | snp | A/G | 0.420255 | 0.183066 | intron-variant | USP10 | GRCh38.p7 | 16:84752066 | CAACTCCATTTTTCT[A/G]TATGTCAGCAGATTT | 9100 |
rs4783058 | snp | G/T | 0.00597534 | 0.0543715 | intron-variant | USP10 | GRCh38.p7 | 16:84756994 | GTCAGGTGGACCCAG[G/T]TTCAcaggtcatttc | 9100 |
rs5818506 | in-del | -/T | 0.360842 | 0.224085 | intron-variant | USP10 | GRCh38.p7 | 16:84731776 | AGCTCTTTTTTTTTT[-/T]GTGATAGTCTGTGCT | 9100 |
rs6564067 | snp | A/G | 0.273587 | 0.248885 | intron-variant | USP10 | GRCh38.p7 | 16:84700806 | CAGTAGCTAAAGCTT[A/G]GGGGCCCTTTACAAT | 9100 |
rs6564068 | snp | C/T | 0.456568 | 0.140818 | intron-variant | USP10 | GRCh38.p7 | 16:84711144 | GAGATTTCAGTTTGG[C/T]TTGGCATTCATTAAG | 9100 |
rs6564069 | snp | A/T | 0.494013 | 0.0543839 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719921 | CTTAGCTAGTATACC[A/T]CTTTTTGCATTCTTT | 9100 |
rs6564070 | snp | A/T | 0.29432 | 0.24604 | intron-variant | USP10 | GRCh38.p7 | 16:84724011 | AATGAATATGAAAGT[A/T]GGTGGAATCTTGAAC | 9100 |
rs6564071 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | USP10 | GRCh38.p7 | 16:84724826 | TTGGCGAACTTCCTG[C/G]TGTGCATTCACTAGT | 9100 |
rs6564072 | snp | C/G | 0.316726 | 0.240931 | intron-variant | USP10 | GRCh38.p7 | 16:84727881 | ATGCAGTACTTTTTT[C/G]TAACCTGTCCATATT | 9100 |
rs6564073 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | USP10 | GRCh38.p7 | 16:84732413 | CTCCGTTGTGGAAAT[C/T]GCTAATTCTTCTCAA | 9100 |
rs6564074 | snp | A/C | 0.41325 | 0.18934 | intron-variant | USP10 | GRCh38.p7 | 16:84752644 | AAGACCTGACTTTTG[A/C]ATGATAACAATAGGA | 9100 |
rs6564075 | snp | A/G | 0.493881 | 0.054972 | intron-variant | USP10 | GRCh38.p7 | 16:84752741 | TTTTTCACTGCGAGG[A/G]AGAAGAGGAGCTCAC | 9100 |
rs6564076 | snp | A/G | 0.388587 | 0.208071 | intron-variant | USP10 | GRCh38.p7 | 16:84766813 | GGTAAAGCAAAGATA[A/G]GGAATTCTTACAACG | 9100 |
rs7184644 | snp | A/C | 0.352721 | 0.227922 | intron-variant | USP10 | GRCh38.p7 | 16:84752854 | TGTTACAAAAGTGGA[A/C]CTTAAATGTTTCTTG | 9100 |
rs7185379 | snp | C/G | 0.245631 | 0.249962 | intron-variant | USP10 | GRCh38.p7 | 16:84753109 | GTAGTTGGGACTATA[C/G]GCAGGCACCACCATG | 9100 |
rs7185686 | snp | C/T | 0.381697 | 0.212499 | intron-variant | USP10 | GRCh38.p7 | 16:84765407 | gcccttggtgtcctt[C/T]gaccgacatcttcca | 9100 |
rs7185949 | snp | G/T | 0.39842 | 0.201175 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745642 | AGGGCTTGTTCCGGT[G/T]TCAGAGGATCCTGTA | 9100 |
rs7186451 | snp | C/G | 0.362313 | 0.223351 | intron-variant | USP10 | GRCh38.p7 | 16:84724945 | AGCTAGCACCCATAA[C/G]TTACTGGGCTTTGAT | 9100 |
rs7186685 | snp | C/T | 0.386313 | 0.209568 | intron-variant | USP10 | GRCh38.p7 | 16:84765175 | tgtatatttaaagta[C/T]acacagatgttatga | 9100 |
rs7186789 | snp | G/T | 0.246485 | 0.249975 | intron-variant | USP10 | GRCh38.p7 | 16:84753249 | AGCCTCCCAAAGTGT[G/T]GCCTGAAATAGAACT | 9100 |
rs7187994 | snp | A/G | 0.360632 | 0.224189 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719847 | AAATCTTTGGAGGGC[A/G]TGTTTCGACAGATCA | 9100 |
rs7188464 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | USP10 | GRCh38.p7 | 16:84749917 | CTGTTTTTCAAGTGT[A/G]AACTGTTATTTGAAA | 9100 |
rs7188512 | snp | A/C | 0.43309 | 0.17023 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84720051 | GAAGTTCTGTGCTTG[A/C]TCTTAACACCGGAAG | 9100 |
rs7189781 | snp | A/G | 0.145642 | 0.227177 | intron-variant | USP10 | GRCh38.p7 | 16:84720494 | AGAATAATCTGAAGT[A/G]ACTGAGTAATGATGG | 9100 |
rs7191081 | snp | G/T | 0.11963 | 0.213316 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698962 | TATGTAACGTgggaa[G/T]ggatcttcctgttca | 9100 |
rs7191213 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | USP10 | GRCh38.p7 | 16:84766041 | TGGTATTTCAGTGAC[A/C]CTCTTAGTCTGTTGT | 9100 |
rs7191287 | snp | C/G | 0.165853 | 0.235413 | intron-variant | USP10 | GRCh38.p7 | 16:84765804 | GGCTGGAGTCCCTGG[C/G]CACCTGGCTGTGTGC | 9100 |
rs7195111 | snp | A/C | 0.146985 | 0.227789 | intron-variant | USP10 | GRCh38.p7 | 16:84721052 | gtgcccgccaccatg[A/C]ctgactaatttttgt | 9100 |
rs7196102 | snp | G/T | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699781 | CCCTCTCCCCTTCCG[G/T]ATCCACAGCCAGGCC | 9100 |
rs7197496 | snp | A/G | 0.443195 | 0.158668 | intron-variant | USP10 | GRCh38.p7 | 16:84709224 | ACTCCAAACTGAGAG[A/G]TGTTTCCCAAAGGAA | 9100 |
rs7197843 | snp | C/T | 0.49975 | 0.0111793 | intron-variant | USP10 | GRCh38.p7 | 16:84709272 | TCAGAGAACCGTTCC[C/T]GTGGAAGTGACGTGT | 9100 |
rs7199123 | snp | A/T | 0.439224 | 0.163383 | intron-variant | USP10 | GRCh38.p7 | 16:84742572 | GGATTCGTGGTTTTA[A/T]GAGCCTCTGCCTGCA | 9100 |
rs7199508 | snp | C/G | 0.323197 | 0.239044 | intron-variant | USP10 | GRCh38.p7 | 16:84742680 | TTCGTCTGCCTGGCA[C/G]ATTGGGCTCTGAGCT | 9100 |
rs7199841 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84775766 | CTGTTCCCTCATGGG[C/T]GGACCTTGAGACCTC | 9100 |
rs7201543 | snp | A/T | 0.44755 | 0.153212 | intron-variant | USP10 | GRCh38.p7 | 16:84714935 | ATTATTATTATTATT[A/T]TTTTTTTTTTTTGAG | 9100 |
rs7202154 | snp | G/T | 0.156319 | 0.231784 | intron-variant | USP10 | GRCh38.p7 | 16:84722219 | gtactcttttgtttg[G/T]ttaccttcacctgac | 9100 |
rs7202832 | snp | C/T | 0.463561 | 0.129968 | intron-variant | USP10 | GRCh38.p7 | 16:84758822 | TGTATCCTTCCTGGA[C/T]GCCGTCCGCAAGGCC | 9100 |
rs7203000 | snp | C/T | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84758880 | GTGCATGTGACTTAG[C/T]TCAGCTTCCGTGGGC | 9100 |
rs7203008 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | USP10 | GRCh38.p7 | 16:84758889 | ACTTAGCTCAGCTTC[C/T]GTGGGCCATCTAGCT | 9100 |
rs7203065 | snp | G/T | 0.499087 | 0.0213463 | intron-variant | USP10 | GRCh38.p7 | 16:84714909 | AAAATATTTAAAAAG[G/T]TCTGATTATTATTAT | 9100 |
rs7203333 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84758879 | GGTGCATGTGACTTA[G/T]CTCAGCTTCCGTGGG | 9100 |
rs7203766 | snp | A/T | 0.496314 | 0.0427728 | intron-variant | USP10 | GRCh38.p7 | 16:84767776 | AGCAGAATTATTATT[A/T]TTTTTTTTAATTTAT | 9100 |
rs7205632 | snp | A/T | 0.256061 | 0.249927 | intron-variant | USP10 | GRCh38.p7 | 16:84762796 | GATATGTGTTTAGTC[A/T]GTTTCTCCTTTTCCT | 9100 |
rs7205708 | snp | G/T | 0.255224 | 0.249945 | intron-variant | USP10 | GRCh38.p7 | 16:84762569 | GGTGGCACACACCTG[G/T]AGTCCCAGCTACTCG | 9100 |
rs7205741 | snp | A/G | 0.190519 | 0.242821 | intron-variant | USP10 | GRCh38.p7 | 16:84762626 | AACCCGGGAGCTGGA[A/G]GTTGCACTGAGCTGA | 9100 |
rs7206264 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | USP10 | GRCh38.p7 | 16:84713822 | TTGGAACTGAGTTCT[A/G]TAGTTTGCAGAGTCA | 9100 |
rs7206710 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84756026 | GCTTCCATTTGGTGG[C/T]TTCAACCCCTGACCT | 9100 |
rs7206900 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84756080 | GATTGGGCTAAGCAT[C/G]CTTCCCCACCCCCCG | 9100 |
rs7498187 | snp | A/G | 0.290201 | 0.246747 | intron-variant | USP10 | GRCh38.p7 | 16:84736964 | CGGCTAATTTTTTGT[A/G]GTTTTAGTAGAGGCG | 9100 |
rs7498516 | snp | C/T | 0.292266 | 0.246401 | intron-variant | USP10 | GRCh38.p7 | 16:84740846 | AGGTCAACTCTTCAC[C/T]TCCTGGTCTGTTACT | 9100 |
rs7501406 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84771666 | ctgaggtcaggagtt[C/T]aagaccagcctggcc | 9100 |
rs8044259 | snp | A/G | 0.418007 | 0.185132 | intron-variant | USP10 | GRCh38.p7 | 16:84707278 | ATGAATGAAATGTGC[A/G]TTTAGAAACTTTAAT | 9100 |
rs8044557 | snp | C/G | 0.0376037 | 0.131863 | intron-variant | USP10 | GRCh38.p7 | 16:84707221 | AATCTTTCACACTGT[C/G]ACTTCCCCTTAGTAG | 9100 |
rs8044808 | snp | C/T | 0.437542 | 0.165312 | intron-variant | USP10 | GRCh38.p7 | 16:84752569 | GTTGAAAGAGGAATT[C/T]AAATAGAGCGAAGAG | 9100 |
rs8044948 | snp | A/T | 0.358515 | 0.225221 | intron-variant | USP10 | GRCh38.p7 | 16:84716128 | TCCCACAGGGTAGGA[A/T]GGGGAGCTGGCCAGT | 9100 |
rs8045120 | snp | G/T | 0.279726 | 0.248226 | intron-variant | USP10 | GRCh38.p7 | 16:84707543 | TGTTGTTGTTGTTCC[G/T]TTGTTTCATAATATG | 9100 |
rs8045259 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84765458 | gaaccactcttttcc[C/G]tatctctgtagtttc | 9100 |
rs8045503 | snp | C/T | 0.423257 | 0.180228 | intron-variant | USP10 | GRCh38.p7 | 16:84701937 | CATAATTTTCTTCTT[C/T]TTTTTTTTTTTTTTT | 9100 |
rs8046664 | snp | C/T | 0.358515 | 0.225221 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84716253 | TTTCTCCTTGGCAAA[C/T]CATCTGTACTATCTG | 9100 |
rs8047286 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719802 | TTATTAGGATTTTTG[C/T]TGGTAAAGCAAGCTA | 9100 |
rs8047390 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84741526 | TTCTTTGAGTTCACC[C/G]TCCTCCCTGTGCAGT | 9100 |
rs8048680 | snp | A/G | 0.357451 | 0.225731 | intron-variant | USP10 | GRCh38.p7 | 16:84729102 | cgtgtctggccAAGC[A/G]ACACTTTGTCTTTTG | 9100 |
rs8048989 | snp | C/T | 0.494774 | 0.0508504 | intron-variant | USP10 | GRCh38.p7 | 16:84729230 | TATGGATTATTTTAT[C/T]ACATCATTCATAATC | 9100 |
rs8049587 | snp | C/G | 0.000116956 | 0.0076462 | intron-variant | USP10 | GRCh38.p7 | 16:84772702 | TAATGCATACATAAG[C/G]TCGGGAGTGTTCGTG | 9100 |
rs8050719 | snp | A/G | 0.448452 | 0.152042 | intron-variant | USP10 | GRCh38.p7 | 16:84746862 | ttttgactctttcat[A/G]agaacatttagctta | 9100 |
rs8050833 | snp | C/G | 0.295088 | 0.245901 | intron-variant | USP10 | GRCh38.p7 | 16:84724084 | CCTAATTTATCTGCT[C/G]TGTTTCATACAATAG | 9100 |
rs8051512 | snp | C/G | 0.392696 | 0.205275 | intron-variant | USP10 | GRCh38.p7 | 16:84747495 | GTTCTCTTAAATGAG[C/G]AAATGATAGGCCAGA | 9100 |
rs8051593 | snp | A/G | 0.299916 | 0.244966 | intron-variant | USP10 | GRCh38.p7 | 16:84747393 | TTGGGTGGCAATAGG[A/G]TGATAGCAAGCAATG | 9100 |
rs8052070 | snp | C/T | 0.280785 | 0.248097 | intron-variant | USP10 | GRCh38.p7 | 16:84726152 | GTTAATTTGGAACAA[C/T]CTGCATATTTATTCA | 9100 |
rs8056190 | snp | A/G | 0.298398 | 0.245271 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717618 | CATTTTACTAGGTAG[A/G]TAGGAGGAGGCCACT | 9100 |
rs8056245 | snp | C/T | 0.313326 | 0.241847 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717805 | GTCCTAGTCTCTGGT[C/T]CTCAGGTGTATGTGA | 9100 |
rs8056258 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | USP10 | GRCh38.p7 | 16:84739292 | tgttttggtttttga[A/G]acaaagtcttgctct | 9100 |
rs8056348 | snp | A/C | 0.49995 | 0.00499176 | intron-variant | USP10 | GRCh38.p7 | 16:84739534 | CACCTCAGCCTCCCT[A/C]ATTGCTGGGATTACA | 9100 |
rs8056366 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84747803 | aactcctgacctcaa[C/G]tgatctgctcgcttc | 9100 |
rs8058755 | snp | A/G | 0.45645 | 0.140991 | intron-variant | USP10 | GRCh38.p7 | 16:84751597 | AACATAAGTTGATCT[A/G]TAGTCAATGGGTAGT | 9100 |
rs8059257 | snp | A/G | 0.451483 | 0.148002 | intron-variant | USP10 | GRCh38.p7 | 16:84771073 | AAAAAAAAAAAAAGT[A/G]TTATCCAAATGAATA | 9100 |
rs8059636 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | USP10 | GRCh38.p7 | 16:84771268 | ATAAATAGCTTTAAA[A/G]GTTATTTAAAACATC | 9100 |
rs8060744 | snp | G/T | 0.380138 | 0.213458 | intron-variant | USP10 | GRCh38.p7 | 16:84722051 | tactaccacactcca[G/T]atatagaacatttcc | 9100 |
rs8061015 | snp | A/G | 0.17138 | 0.237316 | intron-variant | USP10 | GRCh38.p7 | 16:84739890 | ACTGGCTGTGTTGCA[A/G]TGTAGTGATCGTGAA | 9100 |
rs8063429 | snp | C/G | 0.21875 | 0.248039 | intron-variant | USP10 | GRCh38.p7 | 16:84727962 | agcacaggatccagt[C/G]tagggtcaggaaatg | 9100 |
rs8063610 | snp | C/G | 0.362732 | 0.22314 | intron-variant | USP10 | GRCh38.p7 | 16:84728063 | TTTGAACAGCAGTTT[C/G]TCCTCCCCTCTTTTG | 9100 |
rs8063704 | snp | C/G | 0.0437281 | 0.141251 | intron-variant | USP10 | GRCh38.p7 | 16:84727984 | caggaaatgtattta[C/G]ttatcatgtctctag | 9100 |
rs8064001 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | USP10 | GRCh38.p7 | 16:84714046 | AGGCTTTTCCTGGGC[A/G]CCAGAATAGTAAGGT | 9100 |
rs9673314 | snp | G/T | 0.11228 | 0.208646 | intron-variant | USP10 | GRCh38.p7 | 16:84725575 | CCGGCTAATTTTTTT[G/T]TGTGTTTTTAGTAGA | 9100 |
rs9921311 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | USP10 | GRCh38.p7 | 16:84769272 | GGCTTATCTTGTGTG[C/G]TCTGAGTCAGAAAGA | 9100 |
rs9922892 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP10 | GRCh38.p7 | 16:84774873 | GCTTTTTTCTTTTCC[A/G]TTTTGTAGAGCACCT | 9100 |
rs9926728 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84735964 | GCGGCATGTGGTTGG[A/G]CCTGTGGGTGTGTGA | 9100 |
rs9928400 | snp | A/C | 0.250168 | 0.25 | intron-variant | USP10 | GRCh38.p7 | 16:84749098 | AGATAGTAGAGCAAT[A/C]GAGTCACATTGAATA | 9100 |
rs9928495 | snp | A/G | 0.249038 | 0.249998 | intron-variant | USP10 | GRCh38.p7 | 16:84749159 | ATGGCATTGTTTGAA[A/G]TTTTTTTTGTTGTTT | 9100 |
rs9929223 | snp | A/G | 0.306182 | 0.243605 | intron-variant | USP10 | GRCh38.p7 | 16:84743983 | GAAGGTTACCAGCGG[A/G]GGAGACCAAGAGATA | 9100 |
rs9929430 | snp | A/G | 0.202035 | 0.245356 | intron-variant | USP10 | GRCh38.p7 | 16:84713897 | GACCTGGCGTGTGCC[A/G]TGTCGCTGAAGTGCA | 9100 |
rs9929813 | snp | G/T | 0.383439 | 0.21141 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698123 | GACACTATATTGTAT[G/T]GTTTTCCCCAATttt | 9100 |
rs9931093 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84725453 | tacccgggctggagt[A/G]caaatggcacgattt | 9100 |
rs9932860 | snp | A/C | 0.00126342 | 0.0251021 | intron-variant | USP10 | GRCh38.p7 | 16:84732570 | tcctggctcagcctc[A/C]cgagcagccgggact | 9100 |
rs9932902 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84773524 | TCTACCCTAGGGGCG[C/T]CCTATACCTTCCCGT | 9100 |
rs9934055 | snp | C/T | 0.00154056 | 0.0277112 | intron-variant | USP10 | GRCh38.p7 | 16:84775266 | TCTTCATTAAAACAC[C/T]GATGAAGGGGTTTAC | 9100 |
rs9936114 | snp | A/G | 0.379942 | 0.213577 | intron-variant | USP10 | GRCh38.p7 | 16:84734070 | tcagccgttaaaaat[A/G]ttgcactcaatgtat | 9100 |
rs9936670 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84727459 | AGTGTTAGCTTTaaa[A/C]aaacaaacaaacaaa | 9100 |
rs9937760 | snp | C/T | 0.492823 | 0.0594727 | intron-variant | USP10 | GRCh38.p7 | 16:84713521 | CCCAATGTAAGCTCC[C/T]TGAGGCCCCAATGTA | 9100 |
rs9938879 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | USP10 | GRCh38.p7 | 16:84727702 | GGCTAACAAATGCAA[A/G]TATACAGACATACAA | 9100 |
rs9940211 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84745851 | TATAGAAACAAATGG[C/G]AGGAGAGGGTTGTCG | 9100 |
rs9940230 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84723316 | CACTTACGTTGAATA[A/C]GTCTTATATTTTAAA | 9100 |
rs10220981 | snp | A/G | 0.0387552 | 0.1337 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717631 | AGGTAGGAGGAGGCC[A/G]CTACCTAGGTTATTG | 9100 |
rs10438619 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | USP10 | GRCh38.p7 | 16:84734545 | TCTGTTCCTAGCATG[A/G]GGGCTTTAAGCTTCA | 9100 |
rs10459848 | snp | A/G | 0.183568 | 0.241012 | intron-variant | USP10 | GRCh38.p7 | 16:84721879 | attttttgtgttttc[A/G]tagagacagggtttc | 9100 |
rs10571112 | in-del | -/TG | 0.261332 | 0.249743 | intron-variant | USP10 | GRCh38.p7 | 16:84765256 | CATCACAGTTACCCT[-/TG]TGTGTGTGTGTGTGC | 9100 |
rs10583748 | in-del | -/CT | 0.432651 | 0.170701 | intron-variant | USP10 | GRCh38.p7 | 16:84775898 | CGTCATCTTTTATGC[-/CT]CTGAGTCTTTACCTC | 9100 |
rs10699847 | in-del | -/TTT | | | intron-variant | USP10 | GRCh38.p7 | 16:84720597 | TTTTTTTTTTTTTTT[-/TTT]TTGAGATGGAGCCTC | 9100 |
rs10706586 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84711720 | TGAGGAAGGGCTAGC[-/T]TTTTTTTTTTTTTTT | 9100 |
rs11149677 | snp | C/G | 0.419936 | 0.183362 | intron-variant | USP10 | GRCh38.p7 | 16:84714664 | GCAGGTTTTTTTGGT[C/G]CAATTTTTAGTTGTT | 9100 |
rs11149678 | snp | C/T | 0.29278 | 0.246313 | intron-variant | USP10 | GRCh38.p7 | 16:84726267 | TGAAGCCGAAAGTGG[C/T]GTTTCCCGCAGTTCC | 9100 |
rs11149679 | snp | G/T | 0.444444 | 0.157135 | intron-variant | USP10 | GRCh38.p7 | 16:84738099 | ACAGCTCTCTGCCTT[G/T]TGAAGTGGATGGGTG | 9100 |
rs11149680 | snp | C/T | 0.352721 | 0.227922 | intron-variant | USP10 | GRCh38.p7 | 16:84747301 | GACACCCTTCATTAC[C/T]AGGATGTAGCAGCAA | 9100 |
rs11149681 | snp | A/G | 0.492237 | 0.0618148 | intron-variant | USP10 | GRCh38.p7 | 16:84768566 | TCTAAATCATATTAC[A/G]CAAGGTAATGATCTC | 9100 |
rs11268494 | in-del | -/CGTGTCACTTGGACCTGTGGGTGTGTGAGTGGCGAGGG | | | intron-variant | USP10 | GRCh38.p7 | 16:84736103 | TGTGAGTGGCGAGGG[lengthTooLong]GAGGGCGTGTCACTT | 9100 |
rs11271599 | in-del | -/GGGTGAGGGCCCA | 0.275197 | 0.248727 | intron-variant | USP10 | GRCh38.p7 | 16:84776322 | GCGGTGGGGGCCCAG[-/GGGTGAGGGCCCA]GGGTGAGGGCCCAGT | 9100 |
rs11351357 | in-del | -/G | 0.47743 | 0.103805 | intron-variant | USP10 | GRCh38.p7 | 16:84728982 | TTTTGTATTTTTAGT[-/G]GAGGTGGATTTCACC | 9100 |
rs11363022 | in-del | -/T | 0.488666 | 0.0744214 | intron-variant | USP10 | GRCh38.p7 | 16:84728359 | TTTGGCCTTTTTTAC[-/T]TTTTTTTTTTCTCGC | 9100 |
rs11373011 | in-del | -/GG/GTGGGGGTGTGTGT/T/TGTGT | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84757396 | GAGGGAATGAGAGGG[-/GG/GTGGGGGTGTGTGT/T/TGTGT]GTGTGTGTGTGTGTG | 9100 |
rs11373757 | in-del | -/GAG/GAGAA/GAGAAAAAAA/GAGAGAGAGAGAA | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84764932 | CACGAGAGAGAGAGA[lengthTooLong]AAAAAAAATATATAT | 9100 |
rs11395693 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84765476 | CTTTTTTTTTTTTTT[-/T]AATAAAGATTCCATG | 9100 |
rs11401851 | in-del | -/TT | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84730986 | TTTTTTTTTTTTTTT[-/TT]GACACGGAATCTCTC | 9100 |
rs11418398 | in-del | -/A | 0.0162462 | 0.0886519 | intron-variant | USP10 | GRCh38.p7 | 16:84777208 | GCAGGTGTGAGTGAC[-/A]ACACGGCTCAGCCCA | 9100 |
rs11640943 | snp | C/T | 0.457037 | 0.140127 | intron-variant | USP10 | GRCh38.p7 | 16:84735116 | ACTGCAACTTTGACC[C/T]CCCGCCCCGCCTCAG | 9100 |
rs11641007 | snp | A/C | 0.117886 | 0.21224 | intron-variant | USP10 | GRCh38.p7 | 16:84742465 | TTGTGTCACTAATCT[A/C]TGTATATTTCCCTCC | 9100 |
rs11641059 | snp | G/T | 0.0562307 | 0.157967 | intron-variant | USP10 | GRCh38.p7 | 16:84735238 | gtgtgtgtgtgtgtg[G/T]tgtgtgtgtTTTTAA | 9100 |
rs11641132 | snp | A/G | 0.140242 | 0.224618 | intron-variant | USP10 | GRCh38.p7 | 16:84770540 | cactttgggaggcca[A/G]ggcgggtggatcacg | 9100 |
rs11642223 | snp | C/T | 0.125874 | 0.217008 | intron-variant | USP10 | GRCh38.p7 | 16:84770628 | atacaaaaagttagc[C/T]gggcatggtggcagg | 9100 |
rs11642461 | snp | G/T | 0.113685 | 0.209567 | intron-variant | USP10 | GRCh38.p7 | 16:84736108 | AGTGGCGAGGGGAGG[G/T]CGTGTCACTTCTACA | 9100 |
rs11642462 | snp | A/G | 0.114387 | 0.210022 | intron-variant | USP10 | GRCh38.p7 | 16:84736110 | TGGCGAGGGGAGGGC[A/G]TGTCACTTCTACAGC | 9100 |
rs11642656 | snp | A/G | 0.447162 | 0.153712 | intron-variant | USP10 | GRCh38.p7 | 16:84730635 | AAACAGGAAGTGTGT[A/G]TTAGTGGCTTGGAAT | 9100 |
rs11644121 | snp | A/G | 0.25214 | 0.249991 | intron-variant | USP10 | GRCh38.p7 | 16:84701877 | GATTTAAATGCTTTT[A/G]AGTTTTAGCATGGAG | 9100 |
rs11644667 | snp | C/G | 0.495708 | 0.0461266 | intron-variant | USP10 | GRCh38.p7 | 16:84777659 | AGTCTGACTGGTGGC[C/G]TCAGTCATAAGCACT | 9100 |
rs11645315 | snp | C/T | 0.114036 | 0.209795 | intron-variant | USP10 | GRCh38.p7 | 16:84765974 | AAAGTACTGAAGAGG[C/T]CTCATTGGAGCCTAA | 9100 |
rs11645413 | snp | A/G | 0.161596 | 0.233848 | intron-variant | USP10 | GRCh38.p7 | 16:84738413 | AAGAGGGCATTCTAT[A/G]TATCAGTTTCTAAAC | 9100 |
rs11646367 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84735239 | tgtgtgtgtgtgtgg[G/T]gtgtgtgtTTTTAAG | 9100 |
rs11647063 | snp | G/T | 0.381308 | 0.21274 | intron-variant | USP10 | GRCh38.p7 | 16:84747647 | TGGCTCACTACAACC[G/T]CCGCCTCCTGGGTTC | 9100 |
rs11647467 | snp | G/T | 0.202651 | 0.245475 | intron-variant | USP10 | GRCh38.p7 | 16:84742695 | GATTGGGCTCTGAGC[G/T]CTCTGCCATGCGGTG | 9100 |
rs11649591 | snp | A/G | 0.237882 | 0.249706 | intron-variant | USP10 | GRCh38.p7 | 16:84768621 | ACATTTAATTTTCTG[A/G]CAATCTAATGATGAT | 9100 |
rs11859169 | snp | C/T | 0.423726 | 0.179776 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698600 | tttctttctttcttt[C/T]tttttttttttttga | 9100 |
rs11859963 | snp | A/G | 0.387832 | 0.208572 | intron-variant | USP10 | GRCh38.p7 | 16:84769672 | TGGTGCACTCTGCTT[A/G]TGCTGTTTCTTGAGC | 9100 |
rs11860875 | snp | C/T | 0.0726307 | 0.176182 | intron-variant | USP10 | GRCh38.p7 | 16:84775837 | CTGCCACATCATCTT[C/T]CCTTTCCTTTCTGCC | 9100 |
rs11861011 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718252 | TCTGAAGAGTTGCTT[A/G]TGAGTTCAtttattt | 9100 |
rs11862543 | snp | A/G | 0.162581 | 0.234218 | intron-variant | USP10 | GRCh38.p7 | 16:84764702 | caggtgtggtgacag[A/G]cacctgtaatcccag | 9100 |
rs11862996 | snp | A/G | 0.15665 | 0.231917 | intron-variant | USP10 | GRCh38.p7 | 16:84732414 | TCCGTTGTGGAAATT[A/G]CTAATTCTTCTCAAT | 9100 |
rs11863037 | snp | C/G | 0.190105 | 0.242719 | intron-variant | USP10 | GRCh38.p7 | 16:84732532 | GCTCACTGCAACCTC[C/G]GCCTCCCTGGTTCAA | 9100 |
rs11863406 | snp | G/T | 0.388964 | 0.20782 | intron-variant | USP10 | GRCh38.p7 | 16:84769060 | GTCTTCTCTGTTATA[G/T]ATCTTAGGTTGTGGC | 9100 |
rs11863660 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | USP10 | GRCh38.p7 | 16:84756546 | tgcagtgagccaaga[C/T]tgcaccactgcactc | 9100 |
rs11863989 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84725877 | TTCATGTTTCCCCAA[A/T]TTGAGCTTATTTGGA | 9100 |
rs11864802 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | USP10 | GRCh38.p7 | 16:84774096 | ctcttctaaaaacac[A/G]aaaattagcctagca | 9100 |
rs11867157 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | USP10 | GRCh38.p7 | 16:84702142 | gcccactgcaacctc[C/T]gcctcccgggttcaa | 9100 |
rs12103304 | snp | C/G | 0.379199 | 0.272264 | intron-variant | USP10 | GRCh38.p7 | 16:84756094 | TCCTTCCCCACCCCC[C/G]GCCCCCCATCTCCCA | 9100 |
rs12149617 | snp | A/G | 0.373397 | 0.217424 | intron-variant | USP10 | GRCh38.p7 | 16:84721292 | GATGCCTACAAATAG[A/G]GTGTACTGAAGAATT | 9100 |
rs12149780 | snp | C/T | 0.297382 | 0.245469 | intron-variant | USP10 | GRCh38.p7 | 16:84740019 | GTATCATAAGCATTT[C/T]ATTGTAGCTGATTTA | 9100 |
rs12149794 | snp | A/G | 0.499575 | 0.0145705 | intron-variant | USP10 | GRCh38.p7 | 16:84740189 | GTTATTCTGCTAGAA[A/G]TAACGGCATGCAAAG | 9100 |
rs12232414 | snp | A/C | 0.29432 | 0.24604 | intron-variant | USP10 | GRCh38.p7 | 16:84749648 | CTCAAGTTTGTTTCA[A/C]ATACTCACATTTCTG | 9100 |
rs12443928 | snp | G/T | 0.292008 | 0.246445 | intron-variant | USP10 | GRCh38.p7 | 16:84746596 | TATAAAGGATGAAAA[G/T]TGCTTCACCTGTATA | 9100 |
rs12445172 | snp | C/G | 0.360842 | 0.224085 | intron-variant | USP10 | GRCh38.p7 | 16:84713410 | CCTTCACACTTGTCA[C/G]CCTGTCTGCTTGCTC | 9100 |
rs12445662 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718956 | cgccaccgcacccag[A/C]taattttcgtatttt | 9100 |
rs12447199 | snp | G/T | 0.492287 | 0.0616198 | intron-variant | USP10 | GRCh38.p7 | 16:84747521 | CCAGACGTCGTTATT[G/T]TGGGCTTCATATATA | 9100 |
rs12447576 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84739222 | caccaccatgcccgg[C/G]taattttttgtattt | 9100 |
rs12448489 | snp | A/G | 0.31882 | 0.240341 | intron-variant | USP10 | GRCh38.p7 | 16:84740416 | GGAATTTGGCCATAC[A/G]TGCTGGGTGGGCAGG | 9100 |
rs12596112 | snp | C/G | 0.245346 | 0.249957 | intron-variant | USP10 | GRCh38.p7 | 16:84757215 | CATTTATTTCAAGGC[C/G]CAGTTCGGTATTCCA | 9100 |
rs12596157 | snp | C/G | 0.244776 | 0.249945 | intron-variant | USP10 | GRCh38.p7 | 16:84757262 | AGCTTTGCAAACTTA[C/G]TCTAATTAAACAGAT | 9100 |
rs12596335 | snp | A/G | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84775079 | TTTACTTGCTGGGGA[A/G]AATGTTGTTAGCCAT | 9100 |
rs12597374 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84731313 | TAactgctcgttgca[A/G]agcagggctacgcca | 9100 |
rs12598223 | snp | A/G | 0.394721 | 0.203852 | intron-variant | USP10 | GRCh38.p7 | 16:84750267 | AAAAAAATTAGATGG[A/G]CGTGGTGGCTCATGG | 9100 |
rs12598730 | snp | C/T | 0.462144 | 0.132269 | intron-variant | USP10 | GRCh38.p7 | 16:84761429 | AGAAGCTGGTATACC[C/T]GTGGCTATGGTTGCT | 9100 |
rs12599287 | snp | A/G | 0.26518 | 0.249539 | intron-variant | USP10 | GRCh38.p7 | 16:84761943 | AGAGCATGCACTCAC[A/G]TGAACAGCTGCTGTC | 9100 |
rs12599947 | snp | A/C/G | 0.000269441 | 0.0116043 | intron-variant | USP10 | GRCh38.p7 | 16:84762966 | TCAGTTCACAGTAAC[A/C/G]TGATTATATTTGACC | 9100 |
rs12600094 | snp | A/G | 0.184203 | 0.241186 | intron-variant | USP10 | GRCh38.p7 | 16:84723235 | AATGGATCACATGGT[A/G]ATTGTTAATGATTTT | 9100 |
rs12716755 | snp | A/G | 0.488545 | 0.074807 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699678 | CGACCTCAGCCCGCG[A/G]CTCCCGGGCTCCGGG | 9100 |
rs12920732 | snp | C/T | 0.355525 | 0.226637 | intron-variant | USP10 | GRCh38.p7 | 16:84747007 | AAACATTAGCCTGGG[C/T]CTGCACAGGGTCAGG | 9100 |
rs12922301 | snp | A/G | 0.357877 | 0.225527 | intron-variant | USP10 | GRCh38.p7 | 16:84761264 | GTGGAGGCAAAATAA[A/G]GTGGGTGCTCAGGAA | 9100 |
rs12922556 | snp | A/G | 0.396 | 0.202938 | intron-variant | USP10 | GRCh38.p7 | 16:84750684 | ATCACAAATAGAGCC[A/G]TTTTGTATTTGATGT | 9100 |
rs12922593 | snp | A/T | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84712159 | GAAAGAAATCGCAGT[A/T]TTTTGTGTGTATGGC | 9100 |
rs12923205 | snp | A/G | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84735197 | TGCCAGGCCCGGGTG[A/G]TGTGTGTGTGTGTGT | 9100 |
rs12924359 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84700034 | AGAAGATGGCGGCGG[C/T]GGGGGAAGCAGCGTG | 9100 |
rs12929725 | snp | A/C | 0.35445 | 0.227135 | intron-variant | USP10 | GRCh38.p7 | 16:84731273 | TGTGAGCCACCGCTC[A/C]CGGCCTCTACTTTTT | 9100 |
rs12932018 | snp | A/G | 0.406221 | 0.195179 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84762997 | TTTTCAGGGTCGACA[A/G]GAAGATGCTGAGGAA | 9100 |
rs12932847 | snp | G/T | 0.480931 | 0.0957637 | intron-variant | USP10 | GRCh38.p7 | 16:84777170 | CTTTTCAGGCGGTTC[G/T]CAGCGCTCCTGTCAG | 9100 |
rs12932991 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | USP10 | GRCh38.p7 | 16:84764559 | TAATTggccatacgc[A/G]gtggttcatgcctgt | 9100 |
rs12933163 | snp | C/G | 0.386504 | 0.209444 | intron-variant | USP10 | GRCh38.p7 | 16:84764694 | AAATCAACCAGGTGT[C/G]GTGACAGGCACCTGT | 9100 |
rs12933228 | snp | A/G | 0.289942 | 0.246789 | intron-variant | USP10 | GRCh38.p7 | 16:84737085 | GAGCCACCACGCCCG[A/G]CCTAATTTGGTATCT | 9100 |
rs12933276 | snp | C/T | 0.289165 | 0.246913 | intron-variant | USP10 | GRCh38.p7 | 16:84737261 | TGTTTTCACACTGTG[C/T]GTTTAGCATAACTAT | 9100 |
rs12933308 | snp | A/G | 0.29046 | 0.246704 | intron-variant | USP10 | GRCh38.p7 | 16:84737367 | ACTTTGTATTCTTAC[A/G]AATAGTTATATAGTT | 9100 |
rs12933675 | snp | C/T | 0.397633 | 0.201754 | intron-variant | USP10 | GRCh38.p7 | 16:84728400 | gctggagttcagtgg[C/T]gcgatctcggctcac | 9100 |
rs12933927 | snp | A/T | 0.289942 | 0.246789 | intron-variant | USP10 | GRCh38.p7 | 16:84736993 | CGGGGTTTCACCGGG[A/T]TAGCCAGGATGGTCT | 9100 |
rs12934432 | snp | A/T | 0.289683 | 0.24683 | intron-variant | USP10 | GRCh38.p7 | 16:84737307 | TTTTCCCTTGCTCAC[A/T]TTGCATTTGTCTAGG | 9100 |
rs12935354 | snp | C/T | 0.327211 | 0.237778 | intron-variant | USP10 | GRCh38.p7 | 16:84702483 | AATAAATTTGTTTTA[C/T]TTGGTTGCCTACTGT | 9100 |
rs13313554 | snp | C/G | 0.0197687 | 0.0974348 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84697956 | cgacctcaggtgatc[C/G]acccacctcagcctt | 9100 |
rs13331387 | snp | A/C | 0.283158 | 0.247791 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699705 | CGGGGGCCCAGGTGG[A/C]CCCCAGTAGGTGAGG | 9100 |
rs13335256 | snp | C/G | 0 | 0 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84772636 | GACTGGTGGGTGCCA[C/G]AAGCTTATCAAAAAT | 9100 |
rs13335307 | snp | G/T | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698769 | tcccaccaatttttg[G/T]atttttagtagagtt | 9100 |
rs13335383 | snp | A/T | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698956 | CTATTTTATGTAACG[A/T]gggaatggatcttcc | 9100 |
rs13336964 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84709483 | AGTGTGGAAGAGGGG[A/G]TGGTACAACATTTGA | 9100 |
rs13343260 | snp | C/G | 0.379158 | 0.214052 | intron-variant | USP10 | GRCh38.p7 | 16:84765004 | AAACCACCTccggga[C/G]gcagaggttgcagtg | 9100 |
rs16944624 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | USP10 | GRCh38.p7 | 16:84726814 | CCCTTGTACTTTGCT[C/T]CCCCGAATCGCAGGC | 9100 |
rs16974422 | snp | A/G | 0.206642 | 0.246211 | intron-variant | USP10 | GRCh38.p7 | 16:84712039 | TTGCTTTTTAAGGTG[A/G]ACAGAAACACCTTGC | 9100 |
rs16974436 | snp | A/G | 0.182614 | 0.240747 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717888 | ATTCTTGCCAAATGC[A/G]GTTTTTCTGAACATT | 9100 |
rs16974437 | snp | C/G | 0.18325 | 0.240924 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719534 | GGTGTGGCCAGGTTC[C/G]AGGACTGTTGTCTTA | 9100 |
rs16974444 | snp | C/T | 0.347032 | 0.230401 | intron-variant | USP10 | GRCh38.p7 | 16:84720134 | GATTTTCTAGGAGAT[C/T]TGAAGAGTCTGCTGA | 9100 |
rs16974449 | snp | A/C | 0.496175 | 0.0435625 | intron-variant | USP10 | GRCh38.p7 | 16:84721358 | TACTGAGGAATTATT[A/C]TTCTGTAAATGAAAG | 9100 |
rs16974453 | snp | C/T | 0.355311 | 0.226737 | intron-variant | USP10 | GRCh38.p7 | 16:84724904 | TTCTGAAGTTGAAAG[C/T]ACACAATGATTGTTC | 9100 |
rs16974478 | snp | C/G | 0.103438 | 0.202533 | intron-variant | USP10 | GRCh38.p7 | 16:84730925 | AAGTAAAAGGCCTTT[C/G]TTGTTAGTCATAAGA | 9100 |
rs16974500 | snp | A/G | 0.180064 | 0.240019 | intron-variant | USP10 | GRCh38.p7 | 16:84743981 | TTGAAGGTTACCAGC[A/G]GAGGAGACCAAGAGA | 9100 |
rs16974508 | snp | A/G | 0.35574 | 0.226537 | intron-variant | USP10 | GRCh38.p7 | 16:84747469 | ATCTCAGGTACTCTT[A/G]TTGTTCTGAAGTTCT | 9100 |
rs16974515 | snp | G/T | 0.393803 | 0.204501 | intron-variant | USP10 | GRCh38.p7 | 16:84748904 | TTTTGTGTGGACATA[G/T]TGTAAACCCCTACCA | 9100 |
rs16974519 | snp | A/C | 0.355954 | 0.226437 | intron-variant | USP10 | GRCh38.p7 | 16:84749144 | TAGGGCTTAGGGAGA[A/C]TGGCATTGTTTGAAA | 9100 |
rs16974527 | snp | C/T | 0.393065 | 0.205018 | intron-variant | USP10 | GRCh38.p7 | 16:84749216 | ATAAAAGTGGTAAAA[C/T]ATACTCAGTTTGTTA | 9100 |
rs16974532 | snp | A/G | 0.392325 | 0.205532 | intron-variant | USP10 | GRCh38.p7 | 16:84749704 | GCTTAATAAATGCCA[A/G]CTAGTTTTTATGCCA | 9100 |
rs16974535 | snp | A/G | 0.355525 | 0.226637 | intron-variant | USP10 | GRCh38.p7 | 16:84749867 | CAAGGCCATCTCCTC[A/G]GTGTAGGTTATGTGT | 9100 |
rs16974538 | snp | G/T | 0.154993 | 0.231244 | intron-variant | USP10 | GRCh38.p7 | 16:84750052 | GGTTGGAGAGGGATC[G/T]GTGTTTCAGTGACTG | 9100 |
rs16974541 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | USP10 | GRCh38.p7 | 16:84751584 | TTTCCACTTCAGAAA[C/T]ATAAGTTGATCTGTA | 9100 |
rs16974548 | snp | C/G | 0.193028 | 0.243422 | intron-variant | USP10 | GRCh38.p7 | 16:84751668 | TAACCAAGATAGTGT[C/G]TGTTCTTCCAAATTG | 9100 |
rs16974558 | snp | A/G | 0.354019 | 0.227333 | intron-variant | USP10 | GRCh38.p7 | 16:84753505 | TATGTATTTACATGC[A/G]TGCTCATCTTTGCTA | 9100 |
rs16974560 | snp | A/G | 0.356383 | 0.226236 | intron-variant | USP10 | GRCh38.p7 | 16:84754819 | CTCCAGGCCATGCAG[A/G]TTATTCTGGGCCCCT | 9100 |
rs16974564 | snp | A/G | 0.0901694 | 0.192235 | intron-variant | USP10 | GRCh38.p7 | 16:84756303 | GCATGTTATTTAACA[A/G]AGGTTTCAGCCACAC | 9100 |
rs16974592 | snp | A/C | 0.0482946 | 0.147699 | intron-variant | USP10 | GRCh38.p7 | 16:84778534 | TCAGGACAGTCTAGA[A/C]GTAGAGTCAGCCACA | 9100 |
rs16974597 | snp | C/T | 0.000222643 | 0.0105485 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779104 | TGTGCGCTGTGTGTG[C/T]GCCCAGTGCCCGCTT | 9100 |
rs16974598 | snp | A/G | 0.0622301 | 0.165053 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779417 | AAATCCTGCACCAGC[A/G]ACAACACTTGTAAAT | 9100 |
rs16974599 | snp | G/T | 0.129664 | 0.219133 | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780069 | TCAGGTTATGCTTGT[G/T]TAGTATTTTCAAATG | 9100 |
rs17554568 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699620 | GCGAACACTCCCGAG[G/T]CCCGGGCCCAGGTAC | 9100 |
rs17597942 | snp | A/G | 0.38286 | 0.211774 | intron-variant | USP10 | GRCh38.p7 | 16:84778183 | TGCGTAACTACCAGC[A/G]CCATCTCCGCAGTGC | 9100 |
rs17763304 | snp | C/T | 0.281577 | 0.247998 | intron-variant | USP10 | GRCh38.p7 | 16:84737570 | TCCTGCAGGTGCGCT[C/T]TTTTATCAGCTTAGC | 9100 |
rs17764145 | snp | A/G | 0.109461 | 0.206758 | intron-variant | USP10 | GRCh38.p7 | 16:84752579 | GAATTTAAATAGAGC[A/G]AAGAGTGATATTAGA | 9100 |
rs17764258 | snp | C/G | 0.105569 | 0.204058 | intron-variant | USP10 | GRCh38.p7 | 16:84754722 | ACTAGTTCATGCTGT[C/G]TCACAAATAAATGCT | 9100 |
rs17764342 | snp | C/T | 0.277067 | 0.24853 | intron-variant | USP10 | GRCh38.p7 | 16:84756765 | GGTTATTTGAAAATG[C/T]ACCTTTTTAACACTG | 9100 |
rs17830698 | snp | G/T | 0.294832 | 0.245947 | intron-variant | USP10 | GRCh38.p7 | 16:84737355 | TTTGATTTTTGAACT[G/T]TGTATTCTTACAAAT | 9100 |
rs17831494 | snp | A/G | 0.276267 | 0.248616 | intron-variant | USP10 | GRCh38.p7 | 16:84751772 | CAACACCAGAATGTC[A/G]ATTACGGGCCAGTTA | 9100 |
rs28432803 | snp | A/C | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84770772 | GCGAGACTCCGTCCC[A/C]AAAAAAAAAAAAAAA | 9100 |
rs28434701 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84754261 | TAACAGAATGATACG[G/T]TATTTTAGTTTATGA | 9100 |
rs28464791 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84702054 | TTCGCTCTTTTTTTT[C/T]TTTTTTTTTTTTTTT | 9100 |
rs28557394 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84776306 | CCAGGGGTGAGGGCC[C/T]AGCGGTGGGGGCCCA | 9100 |
rs28559797 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84710392 | CTGGGACTCTACTCT[C/T]TGCTCATTTTGGCAT | 9100 |
rs28602709 | snp | G/T | 0.393803 | 0.204501 | intron-variant | USP10 | GRCh38.p7 | 16:84726748 | GGGGAATAAATAGCT[G/T]CTCTAGTTCACAGTC | 9100 |
rs28712261 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84714257 | TGTGGTTTGTTCATG[G/T]TATAGTAGTTTCTTC | 9100 |
rs28735610 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84700917 | CTCTCACATCTTCTC[C/T]CCCCTCCGCCATTAT | 9100 |
rs33973475 | in-del | -/TGCTGGCTTT | | | intron-variant | USP10 | GRCh38.p7 | 16:84738100 | AGCTCTCTGCCTTGT[-/TGCTGGCTTT]GAAGTGGATGGGTGA | 9100 |
rs34058047 | in-del | -/A | 0.462144 | 0.132269 | intron-variant | USP10 | GRCh38.p7 | 16:84771055 | GAGCGAGACTGTCTC[-/A]AAAAAAAAAAAAAAA | 9100 |
rs34073781 | in-del | -/GC | 0.4087 | 0.193169 | intron-variant | USP10 | GRCh38.p7 | 16:84733901 | GTAAATGGTATACTA[-/GC]TATTCAGTTTGTCGT | 9100 |
rs34121691 | snp | C/T | 0.00261887 | 0.0360912 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84760189 | GGCGAATATCCCTCA[C/T]GATTTTATCTCCAAG | 9100 |
rs34132997 | in-del | -/A | 0.275197 | 0.248727 | intron-variant | USP10 | GRCh38.p7 | 16:84767790 | TATTTTTTTTAATTT[-/A]TTTTTTTATTGATAA | 9100 |
rs34139611 | snp | C/T | 0.290977 | 0.246619 | intron-variant | USP10 | GRCh38.p7 | 16:84738867 | AATCAAGCAGCAGCT[C/T]TCATACAGTATTGGG | 9100 |
rs34142894 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84715604 | TTTTATCTCCCTTTT[-/T]GCTTACCCCATTTAT | 9100 |
rs34179694 | snp | A/G | 0.359575 | 0.224707 | intron-variant | USP10 | GRCh38.p7 | 16:84742916 | AATTGAGATGTGTAC[A/G]GCACATCTGTGTCTT | 9100 |
rs34240400 | in-del | -/ATGT/GT/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84735196 | TGCCAGGCCCGGGTG[-/ATGT/GT/T]GTGTGTGTGTGTGTG | 9100 |
rs34268991 | in-del | -/A | | | intron-variant | USP10 | GRCh38.p7 | 16:84706916 | GAGAAGGAGAAACAT[-/A]TTTATTACGAGATAC | 9100 |
rs34284179 | in-del | -/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84707025 | GCCTTTACAGCAACT[-/G]CTGTCCTGTATTATT | 9100 |
rs34327141 | snp | C/T | 0.356597 | 0.226135 | intron-variant | USP10 | GRCh38.p7 | 16:84743385 | CGGGAGGCTGTGTAG[C/T]TCCAGCCTCCTGCAC | 9100 |
rs34425075 | in-del | -/C | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718480 | GTTTTTCTTCTGGCC[-/C]GGGTGCGGTGGCTCA | 9100 |
rs34438310 | snp | A/G | 0.331642 | 0.236293 | intron-variant | USP10 | GRCh38.p7 | 16:84709897 | GTGAAGTGGTTAGCC[A/G]GGAGTCTGGAGAGGA | 9100 |
rs34457873 | snp | G/T | 0.393065 | 0.205018 | intron-variant | USP10 | GRCh38.p7 | 16:84749265 | ACAAATTCCCTTTAG[G/T]GGGCACACTTTTAAG | 9100 |
rs34471572 | in-del | -/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84754538 | GCTTTTGTAGGTTCC[-/C]TTGCAGTTATTGAAC | 9100 |
rs34536612 | snp | A/G | 0.481856 | 0.0935034 | intron-variant | USP10 | GRCh38.p7 | 16:84754908 | CACTTTGGGAATCCA[A/G]GGCAGGCGGATTGCT | 9100 |
rs34541686 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84708825 | TACTAGACACTTTTT[-/T]CAGAACCACATATGA | 9100 |
rs34572123 | in-del | -/A | | | intron-variant | USP10 | GRCh38.p7 | 16:84706621 | CTCGGCTCACTGCAA[-/A]GCTCCGCCTCCCGGG | 9100 |
rs34614679 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84706919 | AAGGAGAAACATATT[-/T]ATTACGAGATACTAA | 9100 |
rs34698474 | in-del | -/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84762360 | CTATTTTGTTTACCC[-/C]AAGACAGAAACTTTT | 9100 |
rs34714014 | in-del | -/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84703222 | TCCAAGTGAATATCC[-/C]TTGTCACTGAGGGGA | 9100 |
rs34780846 | in-del | -/A | | | intron-variant | USP10 | GRCh38.p7 | 16:84755811 | AAAAAAAAAAAAAAA[-/A]TCAGTCACTTGCTGG | 9100 |
rs34801529 | in-del | -/C | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717927 | TGTTGAGATGGTCCC[-/C]AGAAATTTGGGATTC | 9100 |
rs34880822 | in-del | -/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84744327 | GATTCCATTGGGGGG[-/G]TATTTTTAAAATTGG | 9100 |
rs34886268 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84741624 | TTTCAGTGACTGCTT[-/T]CTTGGCCCTTTTTCT | 9100 |
rs34911053 | in-del | -/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84769206 | AAAATAAGGTGCCCC[-/C]AACGTAGAAGACCTG | 9100 |
rs34923260 | snp | A/G | 0.294576 | 0.245994 | intron-variant | USP10 | GRCh38.p7 | 16:84739854 | CTCTGCTCTCCGACC[A/G]TGGACCTGGTCCCAG | 9100 |
rs34969868 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779325 | GAAAATACACAAAAA[-/A]CCCATATTTCTGAAA | 9100 |
rs34978714 | in-del | -/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84705315 | GTCTCACTGCAACTT[-/G]CTGCCTCCCGGGTTC | 9100 |
rs35011551 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84720599 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGCCTCGC | 9100 |
rs35019923 | snp | A/C | 0.358303 | 0.225323 | intron-variant | USP10 | GRCh38.p7 | 16:84748608 | CGCGCCCAGCTGAGA[A/C]TATTATAGTTTCGTT | 9100 |
rs35074844 | in-del | -/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84773976 | AATGGGGGCTGGGCG[-/C]CAGTGGCTCACACCT | 9100 |
rs35210690 | snp | C/G | 0.393065 | 0.205018 | intron-variant | USP10 | GRCh38.p7 | 16:84749251 | TCAGATCCACTACCA[C/G]AAATTCCCTTTAGTG | 9100 |
rs35257446 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | USP10 | GRCh38.p7 | 16:84774709 | TCTCCTGACCTCGTG[A/G]TCGCCCGTCTCAGCC | 9100 |
rs35269236 | snp | C/T | 0.294576 | 0.245994 | intron-variant | USP10 | GRCh38.p7 | 16:84721849 | ACTACAGGCACACGC[C/T]GCCACACCTGGCTAA | 9100 |
rs35299797 | in-del | -/TTG/TTGTTG | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84744070 | TTGTTGTTGTTGTTG[-/TTG/TTGTTG]AATCTTTTTTTGACA | 9100 |
rs35301728 | in-del | -/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84757174 | CATGCAGGCTTGGGG[-/G]TTCAGTTCGTAACTG | 9100 |
rs35304398 | in-del | -/GGGTGAGGGCCCA | | | intron-variant | USP10 | GRCh38.p7 | 16:84776323 | CGGTGGGGGCCCAGG[-/GGGTGAGGGCCCA]GGTGAGGGCCCAGTG | 9100 |
rs35307127 | snp | C/T | 0.386694 | 0.20932 | intron-variant | USP10 | GRCh38.p7 | 16:84764483 | CAGGGGACAGGGAGC[C/T]CCTCCCTTCTACTCT | 9100 |
rs35354296 | in-del | -/A | 0.40386 | 0.197046 | intron-variant | USP10 | GRCh38.p7 | 16:84734264 | GTATTAAAAAAAAAA[-/A]TCTTGCTAACTCTTG | 9100 |
rs35376569 | snp | A/G | 0.0514677 | 0.151937 | intron-variant | USP10 | GRCh38.p7 | 16:84768152 | GGGAAAGTGGCAAGG[A/G]GTGGTCTCTTAATTT | 9100 |
rs35408254 | in-del | -/A | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84755002 | CAGAAAAAAAAAAAA[-/A]GGAGCTGTGTTTTCA | 9100 |
rs35594082 | snp | A/C | 0.387263 | 0.208947 | intron-variant | USP10 | GRCh38.p7 | 16:84763258 | ATTTAGGTAAATTAC[A/C]GTTTATCCCGAACCT | 9100 |
rs35705630 | snp | C/T | 0.46703 | 0.124089 | intron-variant | USP10 | GRCh38.p7 | 16:84709766 | TTGAGCTGGAGTTTT[C/T]CAGGCAGAGAAGCAC | 9100 |
rs35791148 | snp | A/G | 0.483852 | 0.0883933 | intron-variant | USP10 | GRCh38.p7 | 16:84731193 | ACCGTGTTAGCCAGG[A/G]TGGTCTCGATCTTCT | 9100 |
rs35793850 | in-del | -/A | 0.319616 | 0.240112 | intron-variant | USP10 | GRCh38.p7 | 16:84746166 | TCAGCTCTTGAAGAG[-/A]AAAAAAATGTTAAGG | 9100 |
rs35815336 | in-del | -/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84763470 | CGCATACATTTTCCC[-/C]TGAATGATTCAAAGT | 9100 |
rs35820091 | in-del | -/A | | | intron-variant | USP10 | GRCh38.p7 | 16:84729191 | TGTTAAATACAAAAA[-/A]TGATGTCTTAACCTT | 9100 |
rs35825970 | in-del | -/AA | 0.39121 | 0.2063 | intron-variant | USP10 | GRCh38.p7 | 16:84749574 | TAAAAAAAAAAAAAA[-/AA]TTATACACACACAAA | 9100 |
rs35887971 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84755104 | CATAAAGCGTGTTTT[-/T]GAGTCTGTTCGAACG | 9100 |
rs35893650 | snp | C/T | 0.37955 | 0.213815 | intron-variant | USP10 | GRCh38.p7 | 16:84764397 | CTCCCCTGCCTGCTC[C/T]TCTCTTGCACTTCCT | 9100 |
rs35956790 | in-del | -/TTT | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84739076 | CTTTTTTTTTTTTTT[-/TTT]GAGACAGAGTCTTGT | 9100 |
rs36008565 | snp | C/G | 0.444799 | 0.156695 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717440 | CCTCCTTCCCTGACC[C/G]CAGTTCTTTGAAGGC | 9100 |
rs36081182 | snp | A/G | 0.404733 | 0.196361 | intron-variant | USP10 | GRCh38.p7 | 16:84738928 | TGCGGCCCTAGGGCC[A/G]TTCCTGCACTGGCCT | 9100 |
rs36109086 | in-del | -/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84744188 | TAATCAAATCACGTT[-/G]AACTACAGAAGCTGA | 9100 |
rs36122502 | in-del | -/TT | 0.240943 | 0.249836 | intron-variant | USP10 | GRCh38.p7 | 16:84723147 | TGATCACATCCAGGG[-/TT]TTTTTTTTTTTGGCC | 9100 |
rs36196417 | in-del | -/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84735949 | CTCACTTTCATGGGG[-/G]CGGCATGTGGTTGGG | 9100 |
rs41327444 | snp | C/T | 0.1357 | 0.222341 | intron-variant | USP10 | GRCh38.p7 | 16:84758685 | AGCATATTTCAGAAA[C/T]TGATGACATCTAGTG | 9100 |
rs41386649 | snp | C/T | 0.293551 | 0.246177 | intron-variant | USP10 | GRCh38.p7 | 16:84735418 | AAGTGAAAAGTGCAC[C/T]GTATTTCAAGTCTGA | 9100 |
rs41403646 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | USP10 | GRCh38.p7 | 16:84740742 | AGTTTACAAAGAACA[C/G]AGGCTCAGAAGCTAG | 9100 |
rs41422347 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717210 | GCGTATGATTTCAGA[A/G]CTTCACAGACCCTCT | 9100 |
rs41451547 | snp | C/T | 0.243919 | 0.249926 | intron-variant | USP10 | GRCh38.p7 | 16:84704479 | GTCTCTGGAAATGAA[C/T]ATCTACACTGCTGAA | 9100 |
rs45473898 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780017 | TAAAATCTGCCCTTC[A/G]ATCAGCTCGACGTGT | 9100 |
rs55634451 | snp | A/G | 0.146985 | 0.227789 | intron-variant | USP10 | GRCh38.p7 | 16:84723734 | ATCAGCTTTATGGAG[A/G]TATAACGTATGTGCG | 9100 |
rs55638897 | snp | G/T | 0.490287 | 0.0690083 | intron-variant | USP10 | GRCh38.p7 | 16:84777148 | GAGAAGCAATCTCGC[G/T]CACAAGCTTTTCAGG | 9100 |
rs55689438 | snp | C/T | 0.107477 | 0.205395 | intron-variant | USP10 | GRCh38.p7 | 16:84732447 | CTTCTTCTTCTTCTT[C/T]TTTTTTTTTTTCTTT | 9100 |
rs55689833 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | USP10 | GRCh38.p7 | 16:84707519 | ATGCTTTTTTCCACT[A/G]GAGTATTTTGTTGTT | 9100 |
rs55709560 | snp | A/T | 0.484209 | 0.0874434 | intron-variant | USP10 | GRCh38.p7 | 16:84715646 | CCCTCCCTTTTTTTT[A/T]TAAAAAAACAAACAA | 9100 |
rs55719773 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | USP10 | GRCh38.p7 | 16:84747759 | TTTAGTAGAAATGGG[A/G]TTTCACCATGCTGCC | 9100 |
rs55773851 | snp | G/T | 0.0648419 | 0.167978 | intron-variant | USP10 | GRCh38.p7 | 16:84757443 | TGTGTGTGTGTGTGT[G/T]TGTTTTGAATTTTGT | 9100 |
rs55864363 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | USP10 | GRCh38.p7 | 16:84731067 | TTGCTGCAACCTCCA[C/T]CTCCCGGGTTCAAGC | 9100 |
rs55897008 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779270 | GACTCTAACTTCCAA[A/G]TCAAAATCATTTGGT | 9100 |
rs55927324 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | USP10 | GRCh38.p7 | 16:84725962 | TGACCTGGTTATACC[A/G]TTTGCCACTGTGAGG | 9100 |
rs55928403 | snp | C/T | 0.0155937 | 0.0869121 | intron-variant | USP10 | GRCh38.p7 | 16:84764049 | TTTTGCTGTTCTTGT[C/T]GTAAATAGTAGTGTA | 9100 |
rs55928460 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779582 | AGAAAAATAAACATA[A/G]AAAATAAGTTGCTGG | 9100 |
rs55973229 | snp | G/T | 0.288386 | 0.247035 | intron-variant | USP10 | GRCh38.p7 | 16:84714360 | TGGCTCTGGCATCCA[G/T]GCTGGAGTGAGTGGC | 9100 |
rs55976696 | snp | A/T | 0.499872 | 0.0079862 | intron-variant | USP10 | GRCh38.p7 | 16:84715647 | CCTCCCTTTTTTTTT[A/T]AAAAAAACAAACAAG | 9100 |
rs56141709 | snp | C/G/T | 0.0372196 | 0.131242 | intron-variant | USP10 | GRCh38.p7 | 16:84708640 | TCATGTTTTTGTCTT[C/G/T]TGTCACTTTGTTTCA | 9100 |
rs56158152 | snp | G/T | 0.229429 | 0.249152 | intron-variant | USP10 | GRCh38.p7 | 16:84700541 | GCCTCTGCCTGGAGC[G/T]AGCCTCAGAGATTTG | 9100 |
rs56163001 | snp | C/G | 0.293807 | 0.246132 | intron-variant | USP10 | GRCh38.p7 | 16:84703395 | CTTCTGTCCTTGTCT[C/G]TGCATAGACTCACCC | 9100 |
rs56218594 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84714932 | ATTATTATTATTATT[A/T]TTATTTTTTTTTTTT | 9100 |
rs56228021 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84702955 | CGAGATCATGCCACT[-/T]GCACTCCAGCCTGGG | 9100 |
rs56294865 | snp | G/T | 0.0337553 | 0.125452 | intron-variant | USP10 | GRCh38.p7 | 16:84728072 | CAGTTTCTCCTCCCC[G/T]CTTTTGATAACATTC | 9100 |
rs56308535 | snp | C/G | 0.0667028 | 0.170006 | intron-variant | USP10 | GRCh38.p7 | 16:84734537 | TACAGGCATCTGTTC[C/G]TAGCATGAGGGCTTT | 9100 |
rs56345464 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | USP10 | GRCh38.p7 | 16:84720836 | ATCTGCCCACCTCGA[C/T]GTCGCAAAGTGCTGG | 9100 |
rs56404731 | snp | A/G | 0.276267 | 0.248616 | intron-variant | USP10 | GRCh38.p7 | 16:84758416 | TTCTCTAATAATGAT[A/G]CTGTGTTAACATTTT | 9100 |
rs56410536 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | USP10 | GRCh38.p7 | 16:84730099 | CTCCAAAAAACGTGC[C/T]AGGAAATCCCCTCCA | 9100 |
rs56739018 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | USP10 | GRCh38.p7 | 16:84750463 | AAGTAGTTGCAAAAC[A/G]CGACACCCTTGTTAA | 9100 |
rs56767487 | snp | G/T | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84757402 | AATGAGAGGGGTGGG[G/T]GTGTGTGTGTGTGTG | 9100 |
rs56824306 | snp | G/T | 0.223522 | 0.248594 | intron-variant | USP10 | GRCh38.p7 | 16:84735131 | CCCCGCCCCGCCTCA[G/T]GGGGGTTCTCATGCT | 9100 |
rs56950568 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | USP10 | GRCh38.p7 | 16:84714938 | ATTATTATTATTATT[A/T]TTTTTTTTTGAGATG | 9100 |
rs56950885 | in-del | -/A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84755002 | AGAAAAAAAAAAAAA[-/A/G]GGAGCTGTGTTTTCA | 9100 |
rs57023162 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | USP10 | GRCh38.p7 | 16:84732417 | GTTGTGGAAATTGCT[A/G]ATTCTTCTCAATGAC | 9100 |
rs57166816 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84730998 | TTTTTTTTTTTTTTT[-/T]GACACGGAATCTCTC | 9100 |
rs57351008 | snp | C/T | 0.298398 | 0.245271 | intron-variant | USP10 | GRCh38.p7 | 16:84750225 | CCAGCCTGGCCAACA[C/T]AGGGAAATCCCATCT | 9100 |
rs57408326 | in-del | -/A | | | intron-variant | USP10 | GRCh38.p7 | 16:84747364 | GAATTGTGTAAAAAA[-/A]TAAAACACATTCTTT | 9100 |
rs57432502 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | USP10 | GRCh38.p7 | 16:84765356 | TCTTGTCCGATGTTC[C/T]ACATCAGATCTCTAG | 9100 |
rs57475196 | snp | A/G | 0.289683 | 0.24683 | intron-variant | USP10 | GRCh38.p7 | 16:84755002 | CAGAAAAAAAAAAAA[A/G]GGAGCTGTGTTTTCA | 9100 |
rs57563757 | snp | C/G | 0.0689305 | 0.172377 | intron-variant | USP10 | GRCh38.p7 | 16:84748692 | CTTTATTTAAAATAA[C/G]CAAGAAAAGCTTCAT | 9100 |
rs57594387 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84723147 | TGATCACATCCAGGG[-/T]TTTTTTTTTTTTGGC | 9100 |
rs57656289 | snp | G/T | 0.175897 | 0.238765 | intron-variant | USP10 | GRCh38.p7 | 16:84741578 | CCTCTGGAGTTCTGC[G/T]TCCCCCTCCCTCCTT | 9100 |
rs57664580 | snp | C/G | 0.0663309 | 0.169604 | intron-variant | USP10 | GRCh38.p7 | 16:84729904 | ATGGTGTATTTTTTT[C/G]CGTGACATGTTTTCA | 9100 |
rs57798593 | snp | A/G | 0.077417 | 0.180873 | intron-variant | USP10 | GRCh38.p7 | 16:84722874 | TCGTCTTAATTTTAT[A/G]GTACATCAATTTAAA | 9100 |
rs57822650 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84743439 | CTCTCAGCGTCTGTA[A/T]TTTTTCTTCTACAAA | 9100 |
rs57836713 | snp | C/G | 0.00398564 | 0.0444627 | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780042 | ACGTGTTTGTGGAAG[C/G]TGAACCACCACTCAG | 9100 |
rs58027755 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84757401 | AATGAGAGGGGTGGG[-/T]GGTGTGTGTGTGTGT | 9100 |
rs58030267 | in-del | -/TAG | | | intron-variant | USP10 | GRCh38.p7 | 16:84749089 | AGTCTCGTGAGATAG[-/TAG]AGCAATAGAGTCACA | 9100 |
rs58075439 | snp | G/T | 0.0905309 | 0.192535 | intron-variant | USP10 | GRCh38.p7 | 16:84729192 | TGTTAAATACAAAAA[G/T]GATGTCTTAACCTTC | 9100 |
rs58123091 | snp | C/T | 0.123798 | 0.215808 | intron-variant | USP10 | GRCh38.p7 | 16:84771108 | AAGCATCAAAGACTT[C/T]GTAAGTACAGAGAAT | 9100 |
rs58182109 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | USP10 | GRCh38.p7 | 16:84708749 | TTCTGACTTGTAATA[A/G]AATGCAAAATCGGGG | 9100 |
rs58203633 | snp | A/G | 0.031825 | 0.122064 | intron-variant | USP10 | GRCh38.p7 | 16:84747160 | AGCAGAAGCTGTGTC[A/G]TCAGGTTGGATTCCA | 9100 |
rs58253726 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | USP10 | GRCh38.p7 | 16:84702436 | GACAGGATTTAGTTA[C/T]TGGTTCCTGCTCCAG | 9100 |
rs58281036 | in-del | -/GG/TGT | | | intron-variant | USP10 | GRCh38.p7 | 16:84757399 | GGAATGAGAGGGGTG[-/GG/TGT]GGGGTGTGTGTGTGT | 9100 |
rs58284103 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | USP10 | GRCh38.p7 | 16:84731089 | GGTTCAAGCGATTCT[C/T]CTGCATCAGCCTCCT | 9100 |
rs58299117 | snp | C/T | 0.147991 | 0.228242 | intron-variant | USP10 | GRCh38.p7 | 16:84764379 | GTAATGGTTTGCATC[C/T]TGCTCCCCTGCCTGC | 9100 |
rs58450217 | in-del | -/A | | | intron-variant | USP10 | GRCh38.p7 | 16:84730093 | AAAACCCTCCAAAAA[-/A]CGTGCTAGGAAATCC | 9100 |
rs58480742 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | USP10 | GRCh38.p7 | 16:84765322 | ACAAAAGTCCCAAAT[A/G]CAGTGCACTATGAGT | 9100 |
rs58517537 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | USP10 | GRCh38.p7 | 16:84726935 | TGACCCCAGTGTTCT[A/G]ACTCTGGCAGAGTTG | 9100 |
rs58589110 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | USP10 | GRCh38.p7 | 16:84749041 | GTTTGTTGAGGCTTC[A/G]ATAGACAGAACGTAG | 9100 |
rs58643642 | snp | A/G | 0.147656 | 0.228091 | intron-variant | USP10 | GRCh38.p7 | 16:84723292 | TAAAGTGTTCTGTGA[A/G]GCTTAATTCACTTAC | 9100 |
rs58671779 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | USP10 | GRCh38.p7 | 16:84738872 | AGCAGCAGCTCTCAT[A/G]CAGTATTGGGCATGA | 9100 |
rs58682387 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | USP10 | GRCh38.p7 | 16:84750940 | TATACCTAAAAGGCA[C/T]TGGATCAAGAAACAA | 9100 |
rs58798707 | snp | A/T | 0.0689305 | 0.172377 | intron-variant | USP10 | GRCh38.p7 | 16:84750093 | AGATGGTTGCCATTT[A/T]TCAGTAGGAGTCAAC | 9100 |
rs58807397 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | USP10 | GRCh38.p7 | 16:84759312 | ATGTGCCTTCAGGAA[A/G]TGTGGTGTGTCTGTT | 9100 |
rs58812391 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84757402 | ATGAGAGGGGTGGGG[-/T]GTGTGTGTGTGTGTG | 9100 |
rs58935940 | snp | A/G | 0.0980852 | 0.198549 | intron-variant | USP10 | GRCh38.p7 | 16:84720643 | CTGGAGTGCAGTGGT[A/G]CGATCTTGCCTTACT | 9100 |
rs58990454 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | USP10 | GRCh38.p7 | 16:84702682 | AGAATAATGGGAGGT[C/G]GAAAAAGTTACAGTT | 9100 |
rs59034711 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | USP10 | GRCh38.p7 | 16:84701753 | TGTCCCAGTATTTAC[A/G]TTTTATACAACAGTC | 9100 |
rs59043454 | snp | A/T | 0.0689305 | 0.172377 | intron-variant | USP10 | GRCh38.p7 | 16:84750006 | CCCAAGGGAAGGATG[A/T]ATCTAAACACAAAAG | 9100 |
rs59072366 | snp | C/T | 0.0685596 | 0.171987 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84719108 | GTTTAGTTGTTGTTG[C/T]TGTTGTTGTTTTTGC | 9100 |
rs59139404 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84739578 | ATGCCCTGCCCCTTC[C/T]TAAACTTTCTTACAC | 9100 |
rs59141680 | in-del | -/GG/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84757400 | GGAATGAGAGGGGTG[-/GG/T]GGTGTGTGTGTGTGT | 9100 |
rs59190412 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | USP10 | GRCh38.p7 | 16:84765599 | TGTTGTGGCAAATGG[C/T]AGGGTCTTTATTACA | 9100 |
rs59214516 | snp | A/C | 0.0271762 | 0.113356 | intron-variant | USP10 | GRCh38.p7 | 16:84767051 | TCCCCACTACTGTAT[A/C]CCTCTCCAGAACCAG | 9100 |
rs59538429 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | USP10 | GRCh38.p7 | 16:84765492 | TTTTTTTTTTTTTTA[A/G]TAAAGATTCCATGTA | 9100 |
rs59808744 | snp | C/T | 0.181978 | 0.240568 | intron-variant | USP10 | GRCh38.p7 | 16:84722925 | GAACATGAGTTCCTG[C/T]CATTGACAGCAAAGT | 9100 |
rs59864194 | snp | A/T | 0.0980852 | 0.198549 | intron-variant | USP10 | GRCh38.p7 | 16:84720994 | CGCCTGCCGTATTCA[A/T]GCTATTTTCCTGCCT | 9100 |
rs59894880 | in-del | -/ATAT/ATATAT | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84764955 | TATATATATATATAT[-/ATAT/ATATAT]TAGACTTCATCTGCA | 9100 |
rs59937517 | snp | A/C | 0.0275645 | 0.114116 | intron-variant | USP10 | GRCh38.p7 | 16:84751637 | TGGTCACTTTGCTGT[A/C]CTCCACCTGGTTAGA | 9100 |
rs60008347 | snp | A/G | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84754989 | CTAGACTTTGTCCCA[A/G]AAAAAAAAAAAAAGG | 9100 |
rs60131277 | snp | C/G | 0.0685596 | 0.171987 | intron-variant | USP10 | GRCh38.p7 | 16:84747147 | TACGTACCTAAGAAG[C/G]AGAAGCTGTGTCATC | 9100 |
rs60223469 | snp | G/T | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84757400 | GGAATGAGAGGGGTG[G/T]GGGTGTGTGTGTGTG | 9100 |
rs60566983 | snp | A/G | 0.354235 | 0.227234 | intron-variant | USP10 | GRCh38.p7 | 16:84741193 | GCCTTGAAAAGACTA[A/G]CCAAACGTTTTATCT | 9100 |
rs60664037 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | USP10 | GRCh38.p7 | 16:84724127 | GGAAGTTATTCAATA[A/G]TGAGGGCTATCTATA | 9100 |
rs60755662 | in-del | -/C | 0.382085 | 0.212258 | intron-variant | USP10 | GRCh38.p7 | 16:84770769 | GCGAGACTCCGTCCC[-/C]AAAAAAAAAAAAAAA | 9100 |
rs60830776 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | USP10 | GRCh38.p7 | 16:84750566 | GACGAACATGTGACG[C/T]TTGAAATTGAACGTA | 9100 |
rs60875796 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | USP10 | GRCh38.p7 | 16:84768465 | AGTTATGCCTCTTAA[A/G]TCAGTTGCTTAACCA | 9100 |
rs60900812 | snp | G/T | 0.0755793 | 0.179102 | intron-variant | USP10 | GRCh38.p7 | 16:84760114 | TGATGATGTTGCTTT[G/T]TTCATCATTTATGAG | 9100 |
rs60972366 | snp | C/G | 0.204189 | 0.245767 | intron-variant | USP10 | GRCh38.p7 | 16:84773547 | CTTCCCGTGAAGACT[C/G]AGACACTGTCTCTCC | 9100 |
rs60997847 | snp | C/G | 0.0689305 | 0.172377 | intron-variant | USP10 | GRCh38.p7 | 16:84748673 | TTAGGGAGATTTTCT[C/G]TATCTTTATTTAAAA | 9100 |
rs61082930 | snp | A/C | 0.0379877 | 0.132479 | intron-variant | USP10 | GRCh38.p7 | 16:84768689 | AGCTTATTTATGTTC[A/C]TGATACCGTAGGGTA | 9100 |
rs61118010 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84706174 | AGGTGTGAGCCACCG[C/T]GCCTAGCCTCCCTAT | 9100 |
rs61123209 | snp | A/G | 0.336245 | 0.234652 | intron-variant | USP10 | GRCh38.p7 | 16:84721579 | GTCTCCCAGGCTGGA[A/G]TGCAGTGGTGTGATC | 9100 |
rs61139585 | in-del | -/AT/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84714932 | TTATTATTATTATTA[-/AT/T]TTATTTTTTTTTTTT | 9100 |
rs61143707 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | USP10 | GRCh38.p7 | 16:84750182 | GGAGGTTGAGGTGGG[C/T]GGATCCCTTGAGGCC | 9100 |
rs61274531 | snp | C/G | 0.0689305 | 0.172377 | intron-variant | USP10 | GRCh38.p7 | 16:84748549 | CCTCAAGTGATCCTC[C/G]TGCCTCAGCCTCTCA | 9100 |
rs61633079 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | USP10 | GRCh38.p7 | 16:84729647 | TAGCCCGTTCCTTTA[C/T]TTCAGTTATAAAATC | 9100 |
rs61760198 | snp | C/G | 0.000659321 | 0.0181446 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745516 | GTCCTGGGCCAGCCT[C/G]TTTCATGATTCTAAG | 9100 |
rs61760199 | snp | A/G | 0.00588075 | 0.0539054 | synonymous-codon, nc-transcript-variant, intron-variant | USP10 | GRCh38.p7 | 16:84759422 | GAAGTTCATTCCTCT[A/G]TATTCCAAAGTGCAA | 9100 |
rs61760200 | snp | A/G | 0.000905372 | 0.0212571 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779079 | CCGAGTGGACCTGCT[A/G]TAAACCCTGTGTGCG | 9100 |
rs62048813 | snp | C/G | 0.3748 | 0.216622 | intron-variant | USP10 | GRCh38.p7 | 16:84701176 | AAGTCAATCTGACTA[C/G]ACCTCTTTTGAAACA | 9100 |
rs62048814 | snp | A/G | 0.385359 | 0.210185 | intron-variant | USP10 | GRCh38.p7 | 16:84702371 | GGCCGATTTCTCATA[A/G]TTTTCATTTTAAAAG | 9100 |
rs62048815 | snp | A/G | 0.278399 | 0.248382 | intron-variant | USP10 | GRCh38.p7 | 16:84703273 | AATTAATTTGAAGCT[A/G]TTAGTTTTGCCTTAC | 9100 |
rs62048854 | snp | A/G | 0.295854 | 0.245759 | intron-variant | USP10 | GRCh38.p7 | 16:84726455 | TAAACCTTTGCCCAG[A/G]GTTTCTCAACTCAGG | 9100 |
rs62048855 | snp | C/T | 0.296109 | 0.245711 | intron-variant | USP10 | GRCh38.p7 | 16:84726638 | TATTTTTTTCCACAT[C/T]CTCTTGAGAAAGGAT | 9100 |
rs62048856 | snp | A/C | 0.287606 | 0.247155 | intron-variant | USP10 | GRCh38.p7 | 16:84730885 | ATTCTGATTTCTTAT[A/C]CTTAGGTATCTTCCC | 9100 |
rs62050861 | snp | A/G | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84747663 | CCGCCTCCTGGGTTC[A/G]AGTGATTCTCCTGCC | 9100 |
rs62050862 | snp | A/G | 0.357877 | 0.225527 | intron-variant | USP10 | GRCh38.p7 | 16:84748343 | GGGTCTCACTCTGTC[A/G]CCCAGGCCGGAATGC | 9100 |
rs62050864 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84749590 | AAAAAAAAAAAAAAT[A/T]ATACACACACAAAAT | 9100 |
rs62050882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84752682 | ACTTGAACATAATTC[A/G]GTCTGGTCTTAGGAG | 9100 |
rs62050884 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84758840 | CGTCCGCAAGGCCAG[A/C]TTGTTGCAGCTGTCC | 9100 |
rs62050885 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | USP10 | GRCh38.p7 | 16:84761869 | CCACCCAGGCCTGCT[A/G]TGAAAAGTCTTCAGC | 9100 |
rs62050887 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84770769 | AGAGCGAGACTCCGT[A/C]CCCAAAAAAAAAAAA | 9100 |
rs62050888 | snp | C/G | 0.491936 | 0.0629843 | intron-variant | USP10 | GRCh38.p7 | 16:84771025 | TCGCACCACTGCACT[C/G]CAGCCTCGATGACAG | 9100 |
rs62050889 | snp | A/G | 0.0537735 | 0.15575 | intron-variant | USP10 | GRCh38.p7 | 16:84774080 | CGTGGTGAAACCCCA[A/G]CTCTTCTAAAAACAC | 9100 |
rs62050890 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84774373 | TAAGTGGTACTTCTG[C/T]GCACAGTAAGAGCAG | 9100 |
rs62050903 | snp | A/C | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84776061 | CCATTTATTGACCTT[A/C]ACACATGTATTGAAC | 9100 |
rs62737162 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84767790 | TATTTTTTTTAATTT[A/T]TTTTTTTATTGATAA | 9100 |
rs66680106 | in-del | -/GT | | | intron-variant | USP10 | GRCh38.p7 | 16:84757397 | GAGGGAATGAGAGGG[-/GT]GGGGGTGTGTGTGTG | 9100 |
rs67138820 | in-del | -/GC | | | intron-variant | USP10 | GRCh38.p7 | 16:84733902 | TAAATGGTATACTAT[-/GC]ATTCAGTTTGTCGTT | 9100 |
rs67729455 | snp | C/T | 0.292266 | 0.246401 | intron-variant | USP10 | GRCh38.p7 | 16:84712054 | GACAGAAACACCTTG[C/T]AGCTGTGCTTCGTTG | 9100 |
rs68114431 | in-del | -/A | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84762698 | CAAAAAAAAAAAAAA[-/A]GTATATTTATTGAAG | 9100 |
rs71151242 | in-del | -/CACACACACACACACACACACACA | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84735214 | TAAAAACACACACAC[-/CACACACACACACACACACACACA]CACACACACACACAC | 9100 |
rs71151243 | in-del | -/CAAAAGCCAG | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84738101 | TTCACCCATCCACTT[-/CAAAAGCCAG]CACAAGGCAGAGAGC | 9100 |
rs71151244 | in-del | -/A | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84747555 | GTGAGACTGCATCTC[-/A]AAAAAAAAAAAAAAA | 9100 |
rs71151245 | in-del | -/TT | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84750421 | CTATTAAGTTTTGGG[-/TT]TTTTTTTTTTTTTTT | 9100 |
rs71384832 | multinucleotide-polymorphism | AA/TT | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84715646 | CCCTCCCTTTTTTTT[AA/TT]AAAAAAACAAACAAG | 9100 |
rs71384834 | in-del | -/TGTG | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84757445 | GTGTGTGTGTGTGTG[-/TGTG]TTTTGAATTTTGTAA | 9100 |
rs71384836 | in-del | -/GCTG | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84769585 | TTCAGTTGTGCATTG[-/GCTG]TGGGTGACTGTCGGC | 9100 |
rs71384837 | in-del | -/G | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84774766 | GAGCCACCGTGCCTG[-/G]CCTGTAATTGAAGTT | 9100 |
rs71386865 | snp | G/T | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84721231 | GTTGTGTAGCACTGG[G/T]AGGTCTTTGGACCAA | 9100 |
rs71386866 | snp | C/G | 0.0931795 | 0.194698 | synonymous-codon, nc-transcript-variant, intron-variant | USP10 | GRCh38.p7 | 16:84758765 | AGTGTCGTTGCAACC[C/G]CGTGGGCTGATCAAT | 9100 |
rs71392780 | in-del | -/AAA | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84739062 | CAAAAAAAAAAAAAA[-/AAA]GGTTTAGGAAGAAAA | 9100 |
rs71642391 | in-del | -/TG | | | intron-variant | USP10 | GRCh38.p7 | 16:84764946 | AAAAAAAAATATATA[-/TG]TATATATATTAGACT | 9100 |
rs71960808 | in-del | -/GT | | | intron-variant | USP10 | GRCh38.p7 | 16:84765267 | CACAGTTACCCTTGT[-/GT]GTGTGTGTGTGCACA | 9100 |
rs72058844 | in-del | -/TAG | 0.0659589 | 0.169201 | intron-variant | USP10 | GRCh38.p7 | 16:84749086 | AGGAGTCTCGTGAGA[-/TAG]TAGAGCAATAGAGTC | 9100 |
rs72416398 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84707776 | AACAATTTTTTTTTT[-/T]CTTAAGAAATATTTT | 9100 |
rs72528199 | in-del | -/G | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84776322 | AGCGGTGGGGGCCCA[-/G]GGGTGAGGGCCCAGT | 9100 |
rs72797561 | snp | C/G | 0.0517044 | 0.152246 | intron-variant | USP10 | GRCh38.p7 | 16:84701920 | GAAATAGTTTGATTT[C/G]TCATAATTTTCTTCT | 9100 |
rs72797562 | snp | G/T | 0.152334 | 0.230133 | intron-variant | USP10 | GRCh38.p7 | 16:84702727 | GGCCAGCGCGGTGGC[G/T]CGTGCCTGTAATCCC | 9100 |
rs72797563 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84703526 | TGAATATCTGTTTCT[A/G]GCCAACAGCTGGATT | 9100 |
rs72797564 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | USP10 | GRCh38.p7 | 16:84703543 | CCAACAGCTGGATTA[C/G]TGTTAATTCTTAAAA | 9100 |
rs72797570 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | USP10 | GRCh38.p7 | 16:84723127 | TGACCGGCTCCGATA[C/G]CTTCTGATCACATCC | 9100 |
rs72797575 | snp | A/G | 0.0966517 | 0.197444 | intron-variant | USP10 | GRCh38.p7 | 16:84736335 | ATGTTAAGATGAAAG[A/G]GCATTCTGCCTTCCT | 9100 |
rs72797584 | snp | C/G | 0.0524604 | 0.153226 | intron-variant | USP10 | GRCh38.p7 | 16:84752320 | ATGAATTGAAAAGAA[C/G]GCTTCTGGGGAAAGT | 9100 |
rs72797587 | snp | G/T | 0.0528381 | 0.153711 | intron-variant | USP10 | GRCh38.p7 | 16:84757668 | TTTTGTTGGTACATA[G/T]TAGGTGTATCTATTT | 9100 |
rs72797595 | snp | G/T | 0.0763149 | 0.179815 | intron-variant | USP10 | GRCh38.p7 | 16:84761461 | ACAGCAAAAGCATGC[G/T]GAGCAGAGTCAGGAA | 9100 |
rs72797596 | snp | C/T | 0.0825414 | 0.185628 | intron-variant | USP10 | GRCh38.p7 | 16:84766546 | GATGGGAGAGAAAGA[C/T]GAATGGACAGCTCAA | 9100 |
rs72799505 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84778088 | TTTTTTTTAAGTAAA[A/T]AACTGTGTGTGTGTG | 9100 |
rs73243904 | snp | C/T | 0.00204176 | 0.0318859 | utr-variant-5-prime, intron-variant | USP10 | GRCh38.p7 | 16:84704814 | ACTGCCATTCTGTCC[C/T]GTCTTGAAACATCAT | 9100 |
rs73243905 | snp | C/G | 0.232359 | 0.249377 | intron-variant | USP10 | GRCh38.p7 | 16:84704914 | CAGCCTGAATTCCTC[C/G]ACTTTCCCTTTTGGG | 9100 |
rs73243908 | snp | G/T | 0.0376037 | 0.131863 | intron-variant | USP10 | GRCh38.p7 | 16:84706052 | TGAAAAAAACAATTT[G/T]TTGTTGTTTTGTAGA | 9100 |
rs73243919 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | USP10 | GRCh38.p7 | 16:84708188 | GGCGTGGTGGCTCAC[A/G]CGTGTAATCCCAGCA | 9100 |
rs73243927 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | USP10 | GRCh38.p7 | 16:84713200 | TTCACCCACTAGTTA[C/T]TTATTGAACTCAGCT | 9100 |
rs73243928 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | USP10 | GRCh38.p7 | 16:84713266 | AACACATTGTCTGTC[C/T]CCGAGACCCTCTGTC | 9100 |
rs73243932 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84714653 | GGTAATGTTTGGCAG[A/G]TTTTTTTGGTCCAAT | 9100 |
rs73243949 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | USP10 | GRCh38.p7 | 16:84724102 | TTTCATACAATAGCA[A/G]TTTTACACAGGAAGT | 9100 |
rs73243970 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | USP10 | GRCh38.p7 | 16:84734225 | ATTTTAACAGTCTTC[A/G]TTCCCATCAGCAGTG | 9100 |
rs73243979 | snp | A/G | 0.039522 | 0.134904 | intron-variant | USP10 | GRCh38.p7 | 16:84741345 | AGGGACCGGGAAGCC[A/G]GGCTGCTCAGCCTCC | 9100 |
rs73243980 | snp | G/T | 0.0383715 | 0.133092 | intron-variant | USP10 | GRCh38.p7 | 16:84741597 | CCCTCCCTCCTTCCA[G/T]CCTGCCTGCCCTTTT | 9100 |
rs73243990 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | USP10 | GRCh38.p7 | 16:84748442 | CCTAGTAGCTGGGAC[C/T]ACAGGTGCCTGGCAC | 9100 |
rs73245611 | snp | C/G | 0.0663309 | 0.169604 | intron-variant | USP10 | GRCh38.p7 | 16:84751123 | AACAATTTCTAGTGA[C/G]CAGTGAGTTGTGTTA | 9100 |
rs73245613 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP10 | GRCh38.p7 | 16:84752003 | TGGCAGCCCTTGTGA[A/G]CTACCATCTAGCATG | 9100 |
rs73245617 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | USP10 | GRCh38.p7 | 16:84752276 | AAGTTGCTGTCTGAA[C/T]AGTTAAGTAGTAAAT | 9100 |
rs73245618 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | USP10 | GRCh38.p7 | 16:84752372 | ATTATATGCCCTTAA[A/G]GAAGGTAAAATAGAT | 9100 |
rs73245626 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP10 | GRCh38.p7 | 16:84754855 | AGTTAAGAACATGAA[A/G]GGAGGCCAGGCACAG | 9100 |
rs73245629 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84755310 | AAGAAAACTGAAGTT[A/G]CTGTTTCACTCCTTC | 9100 |
rs73245631 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84755466 | GCCCCCACTCCTACA[C/T]GCTGCCCCTGCGTGC | 9100 |
rs73245632 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP10 | GRCh38.p7 | 16:84755481 | CGCTGCCCCTGCGTG[C/T]TTCTCACTTCTCTAC | 9100 |
rs73245634 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP10 | GRCh38.p7 | 16:84756280 | TTACTCGCCTTCAGC[A/G]AAAGGCAGCATGTTA | 9100 |
rs73245640 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP10 | GRCh38.p7 | 16:84758309 | GGGTTCTGCAAGATA[C/T]CTTTCTATCTAGTGT | 9100 |
rs73245646 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | USP10 | GRCh38.p7 | 16:84760340 | AGTGTTTGTGTGGTA[A/G]CTGTTGCTTATTGAT | 9100 |
rs73245649 | snp | C/T | 0.200492 | 0.245049 | intron-variant | USP10 | GRCh38.p7 | 16:84761147 | AAATGGAATGAAGTG[C/T]GCCCTCTGCCCTCAG | 9100 |
rs73245650 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84761154 | ATGAAGTGCGCCCTC[C/T]GCCCTCAGTGAGGGA | 9100 |
rs73245656 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP10 | GRCh38.p7 | 16:84763543 | ATCTCCTGCGTAACC[A/G]CAGTCCCTTATCTAA | 9100 |
rs73245662 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP10 | GRCh38.p7 | 16:84768500 | GTACTGAAAGTTTTT[A/G]TGGTTTTACAATGAA | 9100 |
rs73245666 | snp | A/T | 0.0341408 | 0.126114 | intron-variant | USP10 | GRCh38.p7 | 16:84769887 | GTAGTTGTTAGCCTG[A/T]TGTTAGACGGTAGTG | 9100 |
rs73245681 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | USP10 | GRCh38.p7 | 16:84778153 | GAAAAATGGGTAATT[A/T]TTTTTAAAGGCAAAT | 9100 |
rs73261576 | snp | A/G/T | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84704300 | ACCAAAATATGAAAC[A/G/T]TAGTGGGAAGAGCTT | 9100 |
rs74029976 | snp | G/T | 0.123798 | 0.215808 | intron-variant | USP10 | GRCh38.p7 | 16:84715737 | CTAGAAATTCCAGAG[G/T]TAGATCAGGCTTCAA | 9100 |
rs74029977 | snp | A/C | 0.0372196 | 0.131242 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84716250 | TCCTTTCTCCTTGGC[A/C]AATCATCTGTACTAT | 9100 |
rs74029978 | snp | C/G | 0.108755 | 0.206276 | intron-variant | USP10 | GRCh38.p7 | 16:84722400 | TTCATGTACAAGTGT[C/G]TGTGTGGACATAGGT | 9100 |
rs74029980 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP10 | GRCh38.p7 | 16:84724454 | TACAAACAGGGAAGT[A/G]GACACTCAATTGCAG | 9100 |
rs74029989 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | USP10 | GRCh38.p7 | 16:84737898 | TCCACCCTCAGTCAG[C/T]GCCACCTGGCATTAC | 9100 |
rs74029990 | snp | A/C | 0.0759472 | 0.179459 | intron-variant | USP10 | GRCh38.p7 | 16:84738406 | ACAGAAAAAGAGGGC[A/C]TTCTATGTATCAGTT | 9100 |
rs74032675 | snp | A/G | 0.120674 | 0.21395 | intron-variant | USP10 | GRCh38.p7 | 16:84740567 | TATCCTGTGCTTCGG[A/G]GTGCCAGCCATGTAA | 9100 |
rs74032676 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP10 | GRCh38.p7 | 16:84741260 | AGATTTATAAGAAAT[A/G]TGGGAGACCATAAGG | 9100 |
rs74032682 | snp | A/G | 0.109814 | 0.206997 | intron-variant | USP10 | GRCh38.p7 | 16:84751157 | TTGCCTACGGTATTC[A/G]GTACACAACATGCTG | 9100 |
rs74032687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84752428 | GCAGGTCAAGTTTCA[A/G]CCTAGAAGTTGCCTG | 9100 |
rs74032690 | snp | A/G | 0.138886 | 0.22395 | intron-variant | USP10 | GRCh38.p7 | 16:84757028 | TGTTATGTGACCTCA[A/G]TTTTCTCATCTGTAA | 9100 |
rs74032916 | snp | A/T | 0.0599851 | 0.162463 | intron-variant | USP10 | GRCh38.p7 | 16:84701251 | AATGCGAAAACTTTT[A/T]AAAAAATTAGATCTT | 9100 |
rs74032918 | snp | A/G | 0.170084 | 0.236883 | intron-variant | USP10 | GRCh38.p7 | 16:84703862 | TCTCATTGAGAGCAC[A/G]GCGCACTGAAATTCC | 9100 |
rs74032919 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84704267 | GTGGTTGCTGAGGAC[A/C]CTTATTACTGGTACT | 9100 |
rs74033141 | snp | C/T | 0.0640965 | 0.167152 | intron-variant | USP10 | GRCh38.p7 | 16:84773529 | CCTAGGGGCGCCCTA[C/T]ACCTTCCCGTGAAGA | 9100 |
rs74250166 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84728657 | TTATCAAAATTATAA[C/T]TTATGTCCGTCCACT | 9100 |
rs74344192 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | USP10 | GRCh38.p7 | 16:84732095 | TTTATAGTTTTGGTA[C/G]ATGTTGTCAAAGAGC | 9100 |
rs74428272 | snp | C/T | 0.0700422 | 0.173537 | intron-variant | USP10 | GRCh38.p7 | 16:84729546 | ATGGGGAATACTCAT[C/T]GTATGGGAGATGGAA | 9100 |
rs74442068 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | USP10 | GRCh38.p7 | 16:84761225 | AGAGATGCCTTAGAA[A/C]CCAGAGGGGCCCACC | 9100 |
rs74478145 | snp | G/T | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84747581 | TTTTTTTTTTTTTTT[G/T]AGATGCAGTCTCACT | 9100 |
rs74549091 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | USP10 | GRCh38.p7 | 16:84763406 | GATGCTATACACACA[C/G]TGTGTATATATATAT | 9100 |
rs74580832 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | USP10 | GRCh38.p7 | 16:84723774 | ACCCATTTAAAGTGT[A/G]TATTTCCATGAATTT | 9100 |
rs74586827 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84757177 | TGCAGGCTTGGGGTT[C/T]AGTTCGTAACTGATC | 9100 |
rs74612215 | snp | A/G | 0.155325 | 0.23138 | intron-variant | USP10 | GRCh38.p7 | 16:84725459 | GGCTGGAGTGCAAAT[A/G]GCACGATTTCCGCTC | 9100 |
rs74701365 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698614 | TCTTTTTTTTTTTTT[G/T]AGACAGAGACTCGCT | 9100 |
rs74712465 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP10 | GRCh38.p7 | 16:84771307 | CTGGAATCCCAGCAC[A/G]GTGGGAGACTGAGGC | 9100 |
rs74743332 | snp | G/T | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84739257 | GTAGAGACAGGGTTT[G/T]TTTTTTTTTTGTTTT | 9100 |
rs74754154 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | USP10 | GRCh38.p7 | 16:84744121 | ATTTATACTTTCTAA[C/T]TTCTCCTATCCAGTA | 9100 |
rs74812254 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | USP10 | GRCh38.p7 | 16:84727173 | CGTGCTTTTTAGTCT[C/G]CCGTGTGAACTGAAT | 9100 |
rs74814974 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | USP10 | GRCh38.p7 | 16:84754749 | TGCTGGGAAAAAAGT[C/T]GGTTTATAGTTGATT | 9100 |
rs74855443 | snp | A/C | 0.0528381 | 0.153711 | intron-variant | USP10 | GRCh38.p7 | 16:84710915 | GTTGAGCCCTTTCGC[A/C]TGAATAGCAATAACG | 9100 |
rs74883942 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84703499 | GCATATGGCTGAATG[G/T]TACTGTATTGCTGAA | 9100 |
rs74925684 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | USP10 | GRCh38.p7 | 16:84766729 | GAACAGCTCTGTCAC[A/G]GCTGCTAGCCACATC | 9100 |
rs74992092 | snp | C/G/T | 0.0193278 | 0.0963883 | intron-variant | USP10 | GRCh38.p7 | 16:84778860 | TTCGTGTGCAGTGCT[C/G/T]TTCTCACTCTGCTGC | 9100 |
rs75033764 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | USP10 | GRCh38.p7 | 16:84743450 | TGTATTTTTTCTTCT[A/G]CAAAAAGATTTCTAG | 9100 |
rs75158470 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84733647 | GCCTCAACCCACCAA[A/C]TAGATTTGACTGACA | 9100 |
rs75183916 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | USP10 | GRCh38.p7 | 16:84715462 | AAGATGGGTAATGAG[C/G]TAGTCTTGAGAAGGA | 9100 |
rs75198562 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | USP10 | GRCh38.p7 | 16:84758567 | CTTGATGTTGAACTG[A/C]ATGAAGCCTTAACAG | 9100 |
rs75255143 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP10 | GRCh38.p7 | 16:84713577 | TTTGCTTTGTTCACT[A/G]CTGGGGCCCCTAGTC | 9100 |
rs75278199 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP10 | GRCh38.p7 | 16:84733914 | CTATATTCAGTTTGT[C/T]GTTTATTTTAAGCTA | 9100 |
rs75313123 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | USP10 | GRCh38.p7 | 16:84710237 | CTGTGCCACTGCACT[C/G]TAGCCTGGGCAACAG | 9100 |
rs75396687 | snp | G/T | 0.0402882 | 0.136092 | intron-variant | USP10 | GRCh38.p7 | 16:84764361 | TTTTGAGACTTCTTG[G/T]ACGTAATGGTTTGCA | 9100 |
rs75413199 | snp | C/T | 0.19334 | 0.243495 | intron-variant | USP10 | GRCh38.p7 | 16:84748132 | GCACTCCAGCCTGGG[C/T]GACAGAGCCAGACTC | 9100 |
rs75423278 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84716809 | ACACCTTACAATTAC[A/T]TGGGGAGTGACCGCA | 9100 |
rs75446785 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84752737 | TGTTTTTTTCACTGC[A/G]AGGAAGAAGAGGAGC | 9100 |
rs75523541 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84710800 | CCACCAAGAGACACT[A/G]AGTAAGGATCCCTGT | 9100 |
rs75556715 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | USP10 | GRCh38.p7 | 16:84721994 | AGCCATCACGCCCAG[C/T]CCAGTTTGAGTTTTG | 9100 |
rs75621478 | snp | A/C | 0.0444908 | 0.142359 | intron-variant | USP10 | GRCh38.p7 | 16:84731942 | TTCACTGAAAAGTGA[A/C]AGTATTTCAGAAGAT | 9100 |
rs75649714 | snp | A/T | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84739226 | ACCATGCCCGGCTAA[A/T]TTTTTGTATTTTTTA | 9100 |
rs75676073 | snp | A/T | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84729896 | AGTTACTTATGGTGT[A/T]TTTTTTTGCGTGACA | 9100 |
rs75706954 | snp | C/G | 0.00237153 | 0.0343532 | intron-variant | USP10 | GRCh38.p7 | 16:84759858 | ATATATTGTTTAAAA[C/G]TGCACTATTTAACAT | 9100 |
rs75785736 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | USP10 | GRCh38.p7 | 16:84727371 | AATAAGTTAATCTTC[C/T]AGAGGAGAGAAAACA | 9100 |
rs75820212 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | USP10 | GRCh38.p7 | 16:84734837 | ATATGTGTGAGGTGG[C/T]ATCGAACTCCCTGCC | 9100 |
rs75839378 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84765937 | CAAAACTTGTACCAT[C/G]TCCAAGAAGGTTTAC | 9100 |
rs75913670 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | USP10 | GRCh38.p7 | 16:84712738 | GTGACCCCTAAGCTG[C/T]TCTTCAGGTTCTTCA | 9100 |
rs75965700 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | USP10 | GRCh38.p7 | 16:84710437 | CTTTGAGGGGAAAGA[A/G]GTAGGGCATTTCTTT | 9100 |
rs76010925 | snp | A/C | 0.0322114 | 0.122752 | intron-variant | USP10 | GRCh38.p7 | 16:84703181 | TAGCAAAGACAAATA[A/C]ATGAACTTTAACAGT | 9100 |
rs76029916 | snp | A/G/T | 0.00251215 | 0.0353577 | intron-variant | USP10 | GRCh38.p7 | 16:84759518 | GGTGGGGTTTTTCCC[A/G/T]TCTGATAATTAGAAT | 9100 |
rs76085198 | snp | A/T | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84731285 | CTCCCGGCCTCTACT[A/T]TTTTTTTTTTTTTAA | 9100 |
rs76089031 | snp | A/G | 0.49168 | 0.063958 | intron-variant | USP10 | GRCh38.p7 | 16:84777002 | ATTTTGAATAGAGAC[A/G]AGGTTTCGCCCTTTT | 9100 |
rs76147785 | snp | A/C | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84755799 | TGAGACTGTCTCAAA[A/C]AAAAAAAAAAAAATC | 9100 |
rs76176572 | snp | C/G | 0.0376037 | 0.131863 | intron-variant | USP10 | GRCh38.p7 | 16:84710777 | AGAATCACCTGGCAC[C/G]CTGGGTGCCACCAAG | 9100 |
rs76255952 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | USP10 | GRCh38.p7 | 16:84712047 | TAAGGTGGACAGAAA[C/G]ACCTTGCAGCTGTGC | 9100 |
rs76274138 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | USP10 | GRCh38.p7 | 16:84726437 | TGGTTTTCCCACTTC[A/G]TCTAAACCTTTGCCC | 9100 |
rs76302990 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | USP10 | GRCh38.p7 | 16:84768800 | ATTGTAAATATAATA[C/T]AGTCATTGTAAATAT | 9100 |
rs76323200 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | USP10 | GRCh38.p7 | 16:84701817 | TAGCAAAAGTTGGCG[C/G]AACGTAAATGTTAGC | 9100 |
rs76419534 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | USP10 | GRCh38.p7 | 16:84702416 | CAAGTAATGGAATCA[C/T]GTATGACAGGATTTA | 9100 |
rs76444989 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | USP10 | GRCh38.p7 | 16:84766168 | ACAGGTGAATAATAA[G/T]AACCTCAGAAACCTG | 9100 |
rs76457974 | snp | C/T | 0.124837 | 0.216412 | intron-variant | USP10 | GRCh38.p7 | 16:84765101 | CAGCTAACCAAACCA[C/T]GTGTTTTGGTAAGAG | 9100 |
rs76471633 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | USP10 | GRCh38.p7 | 16:84761940 | TGCAGAGCATGCACT[C/G]ACGTGAACAGCTGCT | 9100 |
rs76482468 | snp | A/G | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84736535 | ATTATTTTCTCCAGT[A/G]GAAAAAATGCAGTCA | 9100 |
rs76564465 | snp | C/T | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84728369 | TTTACTTTTTTTTTT[C/T]CTCGCTGTTGCCCAG | 9100 |
rs76575785 | snp | G/T | 0.0448719 | 0.142907 | intron-variant | USP10 | GRCh38.p7 | 16:84708789 | GTGGTTTACTATTTT[G/T]TTTAGAATTAATTTG | 9100 |
rs76582666 | snp | C/G | 0.117188 | 0.211804 | intron-variant | USP10 | GRCh38.p7 | 16:84714292 | AAATGTGGAATGACA[C/G]TTGTTTAGTAAAATG | 9100 |
rs76655253 | snp | A/C | 0.186737 | 0.241863 | intron-variant | USP10 | GRCh38.p7 | 16:84703346 | ATCTCCACAATAATG[A/C]TTCCTACACCCAATT | 9100 |
rs76693763 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717945 | AAATTTGGGATTCGT[A/G]ATCACGTTAGGGTAT | 9100 |
rs76709548 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | USP10 | GRCh38.p7 | 16:84741369 | AGCCTCCTGAGCCAC[C/G]TTTTAATTGGCTGAT | 9100 |
rs76749444 | snp | G/T | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84723159 | GGGTTTTTTTTTTTT[G/T]GGCCTTTTTTCCCCC | 9100 |
rs76760237 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84704245 | GTATTCAGGTGGCAC[A/C]TTAAACGTGGTTGCT | 9100 |
rs76778276 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | USP10 | GRCh38.p7 | 16:84758009 | TGTTTTCAAGCATTT[C/G]TGATGGTTAATTCTA | 9100 |
rs76783913 | snp | A/T | 0.0448719 | 0.142907 | intron-variant | USP10 | GRCh38.p7 | 16:84740081 | TGGCTTCATTTTCGG[A/T]TCTGTTTAATAGTGA | 9100 |
rs76852467 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84725892 | ATTGAGCTTATTTGG[A/G]TCAGGAGAAGAGGGA | 9100 |
rs76871958 | snp | C/T | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84744088 | TCTTTTTTTGACATC[C/T]TTTTTTTTTGTTTTT | 9100 |
rs76884811 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP10 | GRCh38.p7 | 16:84721336 | TGAGAGATTAACAAA[C/T]AGAGCGTACTGAGGA | 9100 |
rs76889386 | snp | C/T | 0.0197687 | 0.0974348 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699257 | GCCAAAACCCAAGGG[C/T]GGACCCACTGGCTGG | 9100 |
rs76956526 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP10 | GRCh38.p7 | 16:84725478 | CGATTTCCGCTCACT[A/G]CAACCTCTGCCTGCT | 9100 |
rs77077751 | snp | A/C/G | 0.0603597 | 0.1629 | intron-variant | USP10 | GRCh38.p7 | 16:84774975 | CACATTTTGTGTCCT[A/C/G]TTACGTCACATGGCT | 9100 |
rs77106696 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84730646 | GTGTGTTAGTGGCTT[G/T]GAATCTTGTTTTCTC | 9100 |
rs77169832 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | USP10 | GRCh38.p7 | 16:84716080 | CTGGCCTGGGGGTGG[C/G]GGTGTGTTGACTTCT | 9100 |
rs77170713 | snp | A/G | 0.00260963 | 0.0360279 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744655 | ATATCAGAGAATTGA[A/G]TTTGGTGTCGATGAA | 9100 |
rs77204762 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | USP10 | GRCh38.p7 | 16:84755136 | GTCAACAACGAAGGG[A/G]AGTTTCAGGCAGATC | 9100 |
rs77219379 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | USP10 | GRCh38.p7 | 16:84769430 | TGGGTGATTTTGTTT[A/G]AAAAATAGAAGCAGT | 9100 |
rs77330018 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | USP10 | GRCh38.p7 | 16:84704048 | TTGCTGTTTAATGCC[A/G]AGCCTAAGCGGCACG | 9100 |
rs77343851 | snp | A/G | 0.0748431 | 0.178382 | intron-variant | USP10 | GRCh38.p7 | 16:84767746 | GTTGTTAGAAATACT[A/G]AGGAGGTGCTATTCA | 9100 |
rs77381225 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | USP10 | GRCh38.p7 | 16:84713683 | CAGAAGCCCACAGTC[A/G]GGTGTGGGAAAGAAG | 9100 |
rs77404885 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84730082 | CCCCTCCCAAGAAAA[C/G/T]CCTCCAAAAAACGTG | 9100 |
rs77446854 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | USP10 | GRCh38.p7 | 16:84760086 | TTCAGCCAGGTGGGA[G/T]GTGGGGGAGTTTTGA | 9100 |
rs77493977 | snp | A/C | 0.0279526 | 0.114869 | intron-variant | USP10 | GRCh38.p7 | 16:84768912 | AATTTAAGAGTATCA[A/C]ATTATAGCTTGGTGG | 9100 |
rs77570454 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | USP10 | GRCh38.p7 | 16:84735841 | TCACAGTAACCTGCA[A/G]AAGGGAAATGCAGGC | 9100 |
rs77635249 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | USP10 | GRCh38.p7 | 16:84738165 | CCTGCTGCAGTCTCT[C/T]GGGTCTGGAGGTTTC | 9100 |
rs77642211 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | USP10 | GRCh38.p7 | 16:84760786 | GCCAGGGAGCCCTTA[C/T]AAAAGGCCCTGGGGC | 9100 |
rs77650136 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | USP10 | GRCh38.p7 | 16:84726283 | GTTTCCCGCAGTTCC[A/G]GCGGGAGAGCTGTAG | 9100 |
rs77666703 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | USP10 | GRCh38.p7 | 16:84767117 | GGAGCATGGAGATGC[A/G]TAATTAAACCCTGGA | 9100 |
rs77676929 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | USP10 | GRCh38.p7 | 16:84751477 | TCTAAGTTAAAAAGG[C/T]GTGGCACCTGTTTAC | 9100 |
rs77730335 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84703883 | CTGAAATTCCAGTGA[A/C]TACTAAGCGGGCCTA | 9100 |
rs77739003 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | USP10 | GRCh38.p7 | 16:84766075 | CCCAAATGCTGCGTA[C/G]CTGAAAGAAAGAGCA | 9100 |
rs77739254 | snp | C/T | 0.0517044 | 0.152246 | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779931 | GTTTAAAGGTGTGTG[C/T]GTGTTTCTTTGAATG | 9100 |
rs77749545 | snp | C/T | 0.25045 | 0.25 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718971 | CTAATTTTCGTATTT[C/T]AGTAGAGACAGGGTT | 9100 |
rs77762177 | snp | G/T | 0.182296 | 0.240658 | intron-variant | USP10 | GRCh38.p7 | 16:84726223 | GCGCCCCCTAGTGCC[G/T]TGCTGTACTGATAGT | 9100 |
rs77818365 | in-del | -/TCTTCGAGACAGAG | 0.296873 | 0.245566 | intron-variant | USP10 | GRCh38.p7 | 16:84774497 | GTTTGTTTGTTTTTT[-/TCTTCGAGACAGAG]TCTTGCTCTGTCACC | 9100 |
rs77835484 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | USP10 | GRCh38.p7 | 16:84774475 | AAGTTTTGTTTTGTT[C/T]TTTTTTTGTTTGTTT | 9100 |
rs77851486 | snp | C/G | 0.0314385 | 0.121371 | intron-variant | USP10 | GRCh38.p7 | 16:84777179 | CGGTTCTCAGCGCTC[C/G]TGTCAGGGGGGCTTG | 9100 |
rs78035613 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | USP10 | GRCh38.p7 | 16:84720299 | TGGTCCGGTTCCAGC[A/G]TATTTTATTAAGTGA | 9100 |
rs78040987 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP10 | GRCh38.p7 | 16:84734737 | TAGATAACGAAGATA[C/T]TTGTCTGTTTTCTTC | 9100 |
rs78050889 | in-del | -/AAA | | | intron-variant | USP10 | GRCh38.p7 | 16:84755810 | CAAAAAAAAAAAAAA[-/AAA]TCAGTCACTTGCTGG | 9100 |
rs78115766 | snp | C/T | 0.00893699 | 0.0662467 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84760264 | GTTAACAAGTCAAGC[C/T]TGTCTGAAAAGGTTT | 9100 |
rs78163285 | snp | C/G | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84738095 | TCTAACAGCTCTCTG[C/G]CTTGTGAAGTGGATG | 9100 |
rs78187081 | snp | G/T | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84750823 | AACTAGGAAAACTGA[G/T]CTCTTGAACAGCTCT | 9100 |
rs78198463 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | USP10 | GRCh38.p7 | 16:84728286 | TTGTCACTCACTGGT[A/G]TTTGCTATAAATATA | 9100 |
rs78233201 | snp | A/C | 0.0283406 | 0.115616 | intron-variant | USP10 | GRCh38.p7 | 16:84757507 | CTGGGATCTGCCAGT[A/C]CAATGTAGTTTAGAA | 9100 |
rs78233420 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | USP10 | GRCh38.p7 | 16:84738629 | GAATGCTTTCTTCTG[A/G]GTGTCAACGTGATGC | 9100 |
rs78309523 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | USP10 | GRCh38.p7 | 16:84740564 | GCGTATCCTGTGCTT[C/T]GGAGTGCCAGCCATG | 9100 |
rs78318000 | snp | A/G | 0.0138799 | 0.0821421 | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780186 | TTTCTATAGCCCACC[A/G]TTTTCAGTATCACCA | 9100 |
rs78318978 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | USP10 | GRCh38.p7 | 16:84727339 | ACAATTTTCCCCCCT[C/T]ATGTGACAGCCTTTG | 9100 |
rs78417536 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | USP10 | GRCh38.p7 | 16:84723474 | AATAAAAACCATTCA[G/T]AGTGATCAAGTTAAG | 9100 |
rs78463846 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | USP10 | GRCh38.p7 | 16:84720120 | ATTAGACAGTCCTAG[A/G]TTTTCTAGGAGATTT | 9100 |
rs78497104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84702629 | CAAATTGAAGGTCTT[A/G]TTTTAAAATTGACTT | 9100 |
rs78530312 | snp | C/T | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84707776 | AACAATTTTTTTTTT[C/T]CTTAAGAAATATTTT | 9100 |
rs78567034 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | USP10 | GRCh38.p7 | 16:84731491 | CTCGAATTCATTTTC[C/T]GGAATTCTTAAGCAG | 9100 |
rs78677906 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84722188 | AGAATTACATTGGCC[C/T]AGAATTACACAAACT | 9100 |
rs78682985 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | USP10 | GRCh38.p7 | 16:84763398 | TATTTTCTGATGCTA[C/T]ACACACACTGTGTAT | 9100 |
rs78693258 | snp | C/G | 0.0715223 | 0.175059 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718472 | TGCATTATAGTTTTT[C/G]TTCTGGCCGGGTGCG | 9100 |
rs78729263 | snp | C/G | 0.254105 | 0.249966 | intron-variant | USP10 | GRCh38.p7 | 16:84772182 | TCTGCCACCCAGGTA[C/G]CTGGGGTTACAGGCG | 9100 |
rs78765389 | snp | C/G/T | 0.0193772 | 0.0965046 | intron-variant | USP10 | GRCh38.p7 | 16:84764447 | CCCGTGGCTTATTCT[C/G/T]TCCCTGCTGGCGCAT | 9100 |
rs78766503 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | USP10 | GRCh38.p7 | 16:84773593 | GAGCTGTGCTTTCTG[C/T]TGACGGGCTTGGCTG | 9100 |
rs78866288 | snp | C/T | 0.22263 | 0.248497 | intron-variant | USP10 | GRCh38.p7 | 16:84746463 | GCAGCCTATTACTCC[C/T]GGGCTGCAAACCTGT | 9100 |
rs78928556 | snp | A/T | 0.0611083 | 0.163768 | intron-variant | USP10 | GRCh38.p7 | 16:84775025 | TTTTTGTGCAACTGA[A/T]GGGATAGAGTGTTGT | 9100 |
rs78952482 | snp | C/T | 0.0327778 | 0.123752 | intron-variant | USP10 | GRCh38.p7 | 16:84729662 | TTTCAGTTATAAAAT[C/T]GAAAGGACCGGTTTT | 9100 |
rs79003402 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84741479 | TTGAACCAGTGCTTA[A/C]AAATGCCCCATGATG | 9100 |
rs79004051 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | USP10 | GRCh38.p7 | 16:84757069 | GTAACTATCTCTGAC[A/G]GTAGGGTTATGATAA | 9100 |
rs79015035 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84768780 | GATTGTAGATCTTCC[A/G]GGTCATTGTAAATAT | 9100 |
rs79017354 | snp | C/T | 0.109814 | 0.206997 | intron-variant | USP10 | GRCh38.p7 | 16:84751113 | AATGGAGCTAAACAA[C/T]TTCTAGTGACCAGTG | 9100 |
rs79035621 | snp | A/C | 0.119978 | 0.213528 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698770 | CCCACCAATTTTTGT[A/C]TTTTTAGTAGAGTTG | 9100 |
rs79054764 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | USP10 | GRCh38.p7 | 16:84743054 | CACACCCGTTTCAAT[C/G]TGGGGAGCCTTGACG | 9100 |
rs79076627 | snp | C/G/T | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84739258 | TAGAGACAGGGTTTG[C/G/T]TTTTTTTTTGTTTTG | 9100 |
rs79103513 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | USP10 | GRCh38.p7 | 16:84709655 | GAGAGAAGTTGCGTG[A/T]CTCAGGAGTTAGGTA | 9100 |
rs79169299 | snp | G/T | 0.0279526 | 0.114869 | intron-variant | USP10 | GRCh38.p7 | 16:84766102 | AGCACCCCTTTTGAG[G/T]CATCAAGACTTGATT | 9100 |
rs79196683 | snp | A/G | 0.110167 | 0.207236 | intron-variant | USP10 | GRCh38.p7 | 16:84725139 | CGTAGTCCATTTTAG[A/G]ACATTTCATCATCCC | 9100 |
rs79214119 | snp | A/T | 0.119281 | 0.213102 | intron-variant | USP10 | GRCh38.p7 | 16:84701535 | CTAATTAACTAGCTT[A/T]TTAGAATTGGTATGA | 9100 |
rs79214942 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | USP10 | GRCh38.p7 | 16:84726760 | GCTTCTCTAGTTCAC[A/T]GTCTTACTTCCCCTA | 9100 |
rs79263353 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | USP10 | GRCh38.p7 | 16:84733800 | CTGAAATTGGGAAAT[A/G]TTGGTCCTGACTGGT | 9100 |
rs79414762 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | USP10 | GRCh38.p7 | 16:84757525 | ATGTAGTTTAGAAAA[C/G]AAAAGCTTATTTTTG | 9100 |
rs79448434 | snp | A/C | 0.0275645 | 0.114116 | intron-variant | USP10 | GRCh38.p7 | 16:84716619 | TGAGCTTTGAAGGAC[A/C]AGTAGGACTTCTTCA | 9100 |
rs79486046 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | USP10 | GRCh38.p7 | 16:84762353 | TTCGTCTTCTATTTT[G/T]TTTACCCAAGACAGA | 9100 |
rs79569269 | snp | G/T | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84769780 | TTTGTGATGTGTCTG[G/T]TTTTCTCTTTTGCTT | 9100 |
rs79656403 | snp | C/G | 0.0490535 | 0.14873 | intron-variant | USP10 | GRCh38.p7 | 16:84769501 | TGAGCTAAGAAGAGT[C/G]TGGCGGTGGACCTCG | 9100 |
rs79666811 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | USP10 | GRCh38.p7 | 16:84730084 | CCTCCCAAGAAAACC[C/T]TCCAAAAAACGTGCT | 9100 |
rs79901544 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84709437 | CAACCTTGCAGCCTT[A/T]GTTAGATGTTACTGT | 9100 |
rs79921567 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | USP10 | GRCh38.p7 | 16:84713467 | ACCCTACATACCCGC[C/T]ATCCTGACGTGTGTG | 9100 |
rs79934545 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84708831 | ACACTTTTTTCAGAA[C/G]CACATATGAAGGACT | 9100 |
rs79958608 | snp | A/T | 0.0221141 | 0.102801 | intron-variant | USP10 | GRCh38.p7 | 16:84740096 | ATCTGTTTAATAGTG[A/T]TAAATATTTGAAAGC | 9100 |
rs79965215 | snp | C/G | 0.0460142 | 0.144533 | intron-variant | USP10 | GRCh38.p7 | 16:84766930 | TGTTTTTCAGTTTCC[C/G]CAGGAAGACTTCCCC | 9100 |
rs79998926 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | USP10 | GRCh38.p7 | 16:84767612 | CATGGCAGGGTGGCT[A/G]CCTTTATGAACCGGT | 9100 |
rs80057396 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | USP10 | GRCh38.p7 | 16:84709388 | GTTGTGTGTCTTGGG[C/T]ACAGAGCTGGAGGGG | 9100 |
rs80086851 | snp | C/G | 0.0425829 | 0.139564 | intron-variant | USP10 | GRCh38.p7 | 16:84737684 | CTGCTGTGCCTCTTA[C/G]TGGCAGTGTCACCTG | 9100 |
rs80122916 | snp | G/T | 0.078151 | 0.181571 | intron-variant | USP10 | GRCh38.p7 | 16:84741819 | GACTGTACAGAGCCT[G/T]TGGGCACTGTCATGG | 9100 |
rs80153232 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | USP10 | GRCh38.p7 | 16:84769319 | GGACCCTTAGCACCT[G/T]CGGGGTGTCCTGCTG | 9100 |
rs80208082 | in-del | -/AAA | | | intron-variant | USP10 | GRCh38.p7 | 16:84749586 | CTTTAAAAAAAAAAA[-/AAA]TTATACACACACAAA | 9100 |
rs80247980 | snp | A/T | 0.0287284 | 0.116357 | intron-variant | USP10 | GRCh38.p7 | 16:84711530 | TGTTGTTGCTCATGG[A/T]TTCGTCAGGTGAGGA | 9100 |
rs80310873 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | USP10 | GRCh38.p7 | 16:84750628 | TCTTTACTAAGGAAC[A/T]TTCCTCATATACTAG | 9100 |
rs111227747 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84741853 | TGCCTCTCTTTCCAG[C/T]CTGCTCAGCTGCTGA | 9100 |
rs111233698 | snp | G/T | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84725539 | CTGAGTAGCTGAGAT[G/T]AGAGGCGCCTGCCAC | 9100 |
rs111234366 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | USP10 | GRCh38.p7 | 16:84747422 | TGTATATATATTTTT[A/C]AGAGTATTTTATTCC | 9100 |
rs111235520 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | USP10 | GRCh38.p7 | 16:84712614 | AGCATGCAAGACCCC[A/G]AGGGGCAGATTTGCC | 9100 |
rs111259714 | snp | A/G | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84764933 | CACGAGAGAGAGAGA[A/G]AAAAAAATATATATA | 9100 |
rs111273437 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84766129 | GATTCAGTCTCAGTT[C/T]TGAGACTGAATCAAC | 9100 |
rs111286908 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | USP10 | GRCh38.p7 | 16:84704497 | CATTTCCAGAGACTT[C/G]TATGTGCTTGGACTG | 9100 |
rs111315175 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | USP10 | GRCh38.p7 | 16:84763456 | ATATATACATACATA[C/T]GCATACATTTTCCCT | 9100 |
rs111316824 | snp | C/T | 0.00153544 | 0.0276651 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745548 | CCTCTTCCTCCTCGC[C/T]GGTGGCCTATGTGGA | 9100 |
rs111334843 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84762611 | CAGGAGAATCGCTTG[A/G]ACCCGGGAGCTGGAG | 9100 |
rs111350281 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717622 | TTACTAGGTAGGTAG[G/T]AGGAGGCCACTACCT | 9100 |
rs111362545 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | USP10 | GRCh38.p7 | 16:84728341 | AAATATATTGAATAA[A/T]TATTTGGCCTTTTTT | 9100 |
rs111451681 | in-del | -/TGGC | 0.372794 | 0.217765 | intron-variant | USP10 | GRCh38.p7 | 16:84769583 | GGTTCAGTTGTGCAT[-/TGGC]TTGTGGGTGACTGTC | 9100 |
rs111471007 | snp | A/G | 0.00150558 | 0.0273957 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745457 | TCACCTCCTGCTGAC[A/G]GCACGGGCTCTGCAT | 9100 |
rs111518935 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84748492 | TATTTTTAGTAGAGA[C/G]CGAGTTTCACCATGT | 9100 |
rs111561696 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | USP10 | GRCh38.p7 | 16:84739341 | CAGTGGCGCGATCTC[G/T]GCTCACTGCAACCTC | 9100 |
rs111562666 | snp | A/C | 0.0023933 | 0.0345097 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699583 | GGATCTTCATAAACC[A/C]GACCCTCCTCGGGGA | 9100 |
rs111586288 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP10 | GRCh38.p7 | 16:84774275 | ACATAAATGGGGGAC[A/G]AGAGGACCTCACTTG | 9100 |
rs111609540 | snp | A/C | 0.0689305 | 0.172377 | intron-variant | USP10 | GRCh38.p7 | 16:84748421 | CAATTCTCCTGCCTC[A/C]GCCTCCCTAGTAGCT | 9100 |
rs111639576 | snp | C/G/T | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84737083 | GTGAGCCACCACGCC[C/G/T]GGCCTAATTTGGTAT | 9100 |
rs111641715 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84766875 | GATTCTTTATTCACA[C/T]CAATTGAAAGATTTA | 9100 |
rs111697466 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84710191 | AAGAGAATCGCTTGA[A/G]CCCGGGAGGCAGAGG | 9100 |
rs111724995 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717718 | GTTGAAGAGGAGATG[C/T]ATCACTTCTTAGTAA | 9100 |
rs111726185 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | USP10 | GRCh38.p7 | 16:84730873 | ATCCTGCAGAACATT[C/G]TGATTTCTTATCCTT | 9100 |
rs111732569 | in-del | -/TGCTGGCTTT | 0.294534 | 0.246537 | intron-variant | USP10 | GRCh38.p7 | 16:84738099 | CAGCTCTCTGCCTTG[-/TGCTGGCTTT]GTGAAGTGGATGGGT | 9100 |
rs111743041 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84704289 | ACTGGTACTATACCA[A/T]AATATGAAACGTAGT | 9100 |
rs111755649 | snp | A/G | 1.66076e-05 | 0.00288158 | intron-variant | USP10 | GRCh38.p7 | 16:84740283 | ATTTTGTTGAATTAA[A/G]ATTTGTTTTCTGATT | 9100 |
rs111767783 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84708216 | GCACTTTGGGAGGTC[A/G]AGGTGGGTGGATCAC | 9100 |
rs111840816 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84749749 | AAGAAGGCAGATGGA[A/C]TAAAAGAATCACGTA | 9100 |
rs111862217 | in-del | -/T | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84765477 | CTCTGTAGTTTCGTC[-/T]TTTTTTTTTTTTTAA | 9100 |
rs111870658 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | USP10 | GRCh38.p7 | 16:84763148 | GTAAACAGGTGTTGC[A/G]TACTCATATGTTATG | 9100 |
rs111892398 | snp | C/G/T | 0.101824 | 0.201941 | intron-variant | USP10 | GRCh38.p7 | 16:84777552 | TGTGTCCCTGGCTCT[C/G/T]CGAAGTACGGGCCCC | 9100 |
rs111892662 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84726351 | TCCTTCTCGCCTTCC[C/T]TGGGCTGAGATGGAG | 9100 |
rs111900319 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | USP10 | GRCh38.p7 | 16:84705425 | TTTAGTAGAGACTGG[G/T]TTTCACCATGTTAGC | 9100 |
rs111937128 | snp | C/T | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84705649 | TCCCATTTGTCTTTG[C/T]TTTATGAAGATGTGC | 9100 |
rs111950406 | snp | C/G | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84777548 | TGGCTGTGTCCCTGG[C/G]TCTCCGAAGTACGGG | 9100 |
rs111951334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84752635 | CTTGTCCGTAAGACC[C/T]GACTTTTGCATGATA | 9100 |
rs111978893 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84743414 | ACACTCACTTGCACG[C/T]AACTGGCCCCTCTCA | 9100 |
rs112006743 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84701025 | CCCTATAAATTGTTG[A/C]ACACTTTTAAACCAT | 9100 |
rs112040808 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84748471 | ACCACGCCAGGCTAA[A/T]TTTTGTATTTTTAGT | 9100 |
rs112067074 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698907 | GCCCACTTATATTTT[C/T]CATGGCATCCCATTT | 9100 |
rs112084421 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | USP10 | GRCh38.p7 | 16:84763478 | ATTTTCCCTGAATGA[G/T]TCAAAGTTAAGTTGC | 9100 |
rs112087944 | snp | A/C | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84716940 | TAGAAGTCCAGAGCC[A/C]TAGGGACAGTCACTG | 9100 |
rs112097874 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84711550 | TCAGGTGAGGAAATT[C/G]TAGTCTCTAGTTTTT | 9100 |
rs112119065 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84748836 | TGAAAGTAAGGGCCT[C/G]TTAATGACTGGTAGT | 9100 |
rs112163045 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718063 | AGATTACTTGTCTTA[C/T]AGAGTTGTAGATGCT | 9100 |
rs112169280 | snp | C/T | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84769763 | TGCCTAGGGAAGACC[C/T]TTTTGTGATGTGTCT | 9100 |
rs112179724 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718819 | TGTTTTTGAGAAGGA[A/G]TCTTTCTCTGTCACC | 9100 |
rs112196993 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84748470 | CACCACGCCAGGCTA[A/T]TTTTTGTATTTTTAG | 9100 |
rs112209761 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | USP10 | GRCh38.p7 | 16:84743880 | GGTATTTTTGGAAGG[C/T]TTTACCACCCATGGG | 9100 |
rs112250763 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84706850 | GGGCCAAGACTATAT[A/G]TATATTTATTCAAGA | 9100 |
rs112255455 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698052 | GTGAGTTTTCACGTC[C/T]CCCAGTTTCTATCCA | 9100 |
rs112279843 | snp | C/G | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84771018 | GCTGAGATCGCACCA[C/G]TGCACTCCAGCCTCG | 9100 |
rs112284636 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | USP10 | GRCh38.p7 | 16:84725221 | TCCTCTCCTCCCAGC[C/G]CTTGGCAACCATGAT | 9100 |
rs112359372 | snp | C/G/T | 0.0745501 | 0.178398 | intron-variant | USP10 | GRCh38.p7 | 16:84771706 | AAACCCCTTCTTTAC[C/G/T]AAAAATACAAAATTA | 9100 |
rs112448324 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP10 | GRCh38.p7 | 16:84773926 | TGTATTTTTATATCC[A/G]CTGCCACCTCCAATA | 9100 |
rs112474835 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | USP10 | GRCh38.p7 | 16:84776630 | CTCCGCCTTCTCCCT[A/G]CACCTCTTCCCCTGG | 9100 |
rs112486414 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84758291 | CAGAGAGGAATGAGA[C/T]GTGGGTTCTGCAAGA | 9100 |
rs112501010 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | USP10 | GRCh38.p7 | 16:84705003 | CGTCTGCGCTGTAAT[C/G]GTGGCTGCTCCTAAG | 9100 |
rs112538444 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84705965 | CACCTCAGGTGATCC[A/G]CCTACCTTGGCCTCC | 9100 |
rs112615923 | snp | A/C/T | 0.0150779 | 0.0856584 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698886 | GGGTGTGAGCCGCTG[A/C/T]GCCTGGCCCACTTAT | 9100 |
rs112623873 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | USP10 | GRCh38.p7 | 16:84776934 | TCTTGTGCCTCAGCC[C/T]CCCGAGTAGCTGGGA | 9100 |
rs112629629 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717240 | CAGAAATGTGTGTAC[A/C]TGCATTCTTTAGGGG | 9100 |
rs112739598 | snp | A/G | 0.256897 | 0.249905 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718857 | GAGTGCAGTGGTGCA[A/G]TCTCAGCTCACTGCA | 9100 |
rs112799054 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84748456 | CTACAGGTGCCTGGC[A/C]CCACGCCAGGCTAAT | 9100 |
rs112815274 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | USP10 | GRCh38.p7 | 16:84726870 | CATTTCCTATGCAAC[C/G]ACAGGACGCGGGAAA | 9100 |
rs112826270 | snp | A/G | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84764935 | CGAGAGAGAGAGAAA[A/G]AAAAATATATATATA | 9100 |
rs112836038 | snp | A/G | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84764934 | ACGAGAGAGAGAGAA[A/G]AAAAAATATATATAT | 9100 |
rs112869911 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | USP10 | GRCh38.p7 | 16:84732662 | CATGTTGGCCAGGCT[A/G]GTCTCGAATTCCTGA | 9100 |
rs112899675 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718190 | ATTAAAAGCAAATGA[A/G]AGATGAGTTTAATTA | 9100 |
rs112902901 | snp | C/T | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84707034 | AGCAACTCTGTCCTG[C/T]ATTATTATAACCATT | 9100 |
rs112948008 | snp | C/T | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84768806 | AATATAATATAGTCA[C/T]TGTAAATATAATATA | 9100 |
rs112951037 | snp | A/G | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84775631 | GCCGGTGATCCCTGC[A/G]TCCTCCCCCACAGGT | 9100 |
rs112966870 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84764720 | CCTGTAATCCCAGCT[A/T]TTAGGGAGGCTGAGG | 9100 |
rs112980413 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84750349 | GGAGGTGGAGGTTCA[G/T]TGAGCCCAGATCGTG | 9100 |
rs112993664 | snp | A/G | 0.0744748 | 0.178019 | intron-variant | USP10 | GRCh38.p7 | 16:84774692 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT | 9100 |
rs112999189 | snp | G/T | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84757401 | GAATGAGAGGGGTGG[G/T]GGTGTGTGTGTGTGT | 9100 |
rs113065646 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | USP10 | GRCh38.p7 | 16:84711611 | GTTCTCTGTTGCTTC[G/T]TACCTCTTTGCTCTT | 9100 |
rs113186976 | snp | C/T | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84778813 | CACATAGGATGCATC[C/T]CTGGAGGGAAGTCGG | 9100 |
rs113204609 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | USP10 | GRCh38.p7 | 16:84772186 | CCACCCAGGTAGCTG[A/G]GGTTACAGGCGCCCA | 9100 |
rs113223148 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | USP10 | GRCh38.p7 | 16:84736163 | AGGTAACATAATTGC[C/T]GCTCAAACATGCAGT | 9100 |
rs113266067 | snp | A/G | | | synonymous-codon, nc-transcript-variant, intron-variant | USP10 | GRCh38.p7 | 16:84759440 | TTCCAAAGTGCAAAG[A/G]CCTTGTACGTCAACA | 9100 |
rs113294300 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718557 | TGTCAGGAGTTCAAG[A/G]CCATCCTGGCCAACA | 9100 |
rs113295058 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | USP10 | GRCh38.p7 | 16:84726742 | GGTGGAGGGGAATAA[A/G]TAGCTTCTCTAGTTC | 9100 |
rs113320086 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718052 | GAGAGATTGGGAGAT[G/T]ACTTGTCTTATAGAG | 9100 |
rs113327958 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | USP10 | GRCh38.p7 | 16:84731697 | ATTTTGCTATTAAGA[C/T]GTTCTGTTGAGTTTT | 9100 |
rs113365471 | snp | A/C | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84775373 | GGGGAGTCACGTGAG[A/C]GTTTTACCTGAAACT | 9100 |
rs113369133 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84769767 | TAGGGAAGACCCTTT[C/G/T]GTGATGTGTCTGTTT | 9100 |
rs113384584 | snp | A/G | 0.399432 | 0.200425 | intron-variant | USP10 | GRCh38.p7 | 16:84748058 | ACTCAGGAGGCTGAG[A/G]CAGGAGAATGGCGTG | 9100 |
rs113396376 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84746751 | ACTTAGGCTGTACTA[C/G/T]GTTGATTTACAAATT | 9100 |
rs113443692 | in-del | -/AG | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84749580 | CCCATCTTTAAAAAA[-/AG]AAAAAAAATTATACA | 9100 |
rs113446464 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | USP10 | GRCh38.p7 | 16:84748250 | TAATGAGAAATGCAT[C/G]GTGGGGTCCTGTTAA | 9100 |
rs113460583 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP10 | GRCh38.p7 | 16:84722716 | AGGCAGACTCCCCCA[C/T]GCCCAGCTAATTTTT | 9100 |
rs113505662 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP10 | GRCh38.p7 | 16:84750652 | ATACTAGACGAAATT[A/G]TATCAGATGCTTTCA | 9100 |
rs113519113 | snp | C/T | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84766447 | CGCTGAGGTCCAGGT[C/T]GGCGCGCAGCAGCGA | 9100 |
rs113531592 | snp | C/G/T | 0.00795939 | 0.0626292 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717223 | AGTTCTGAAATCATA[C/G/T]GCAGAAATGTGTGTA | 9100 |
rs113547173 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84773831 | TGCTCCTGCATCTTC[A/T]CTCGCCTCCAGATCA | 9100 |
rs113596803 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719449 | AAATGCTAAATGAGG[C/T]CTGGACTCCACCCTA | 9100 |
rs113598783 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84704111 | AAGTAATTGAGAAAA[A/G]TGGTATCATCTCCAA | 9100 |
rs113621861 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | USP10 | GRCh38.p7 | 16:84728909 | GTTCACGTAATTCTT[C/G]TGCATCAGCCTCCCA | 9100 |
rs113622944 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718119 | GGGAAAATCTTGGAT[C/T]GGAAGGTTATTTTTG | 9100 |
rs113666236 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | USP10 | GRCh38.p7 | 16:84706731 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACGGTGTT | 9100 |
rs113690501 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84723397 | ATTTATTTGAAGATT[A/G]TATTTGAGAATGAAA | 9100 |
rs113692620 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84745788 | TGTGTGTTAATAGCA[A/G]CGTCTGAAGGATGCC | 9100 |
rs113701208 | snp | G/T | 0.163892 | 0.234703 | intron-variant | USP10 | GRCh38.p7 | 16:84754875 | GCCAGGCACAGTGGC[G/T]CACACCTGTAATCCC | 9100 |
rs113716260 | in-del | -/TG/TGTG/TGTGTG/TGTGTGTG/TGTGTGTGTG/TGTGTGTGTGTGTGTG/TGTGTGTGTGTGTGTGTG/TGTGTGTGTGTGTGTGTGTG | 0.256543 | 0.289697 | intron-variant | USP10 | GRCh38.p7 | 16:84778091 | TTTTAAGTAAATAAC[lengthTooLong]TGTGTGTGTGTGTGT | 9100 |
rs113747778 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84743511 | CTCCGCAGTAGAACA[C/T]CGTTCTTTGGGTATT | 9100 |
rs113748159 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84714953 | TTTTTTTTTTGAGAT[-/G]GAGTCTTGCTCTGTC | 9100 |
rs113749916 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | USP10 | GRCh38.p7 | 16:84715496 | GGATCTCCGCCTCCC[A/C]AAGTGCTGGGATTAC | 9100 |
rs113759840 | snp | C/G | | | utr-variant-5-prime, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84700032 | CGAGAAGATGGCGGC[C/G]GCGGGGGAAGCAGCG | 9100 |
rs113798394 | snp | C/T | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84732739 | AGGCGTGAGCTACTG[C/T]GCCAGGCCTCAATGA | 9100 |
rs113843440 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84739767 | GACTTCTAGCTGTTA[A/C]TGTAGTTAATTAAGG | 9100 |
rs113902372 | snp | C/T | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84730281 | CAGATACTCTATTTT[C/T]CTACCTTTTTTACAC | 9100 |
rs113909552 | snp | G/T | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84765255 | CCATCACAGTTACCC[G/T]TGTGTGTGTGTGTGT | 9100 |
rs113910819 | snp | A/C | 0.00289017 | 0.0379042 | intron-variant | USP10 | GRCh38.p7 | 16:84732426 | ATTGCTAATTCTTCT[A/C]AATGACTTCTTCTTC | 9100 |
rs113924384 | in-del | -/A | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84754990 | TAGACTTTGTCCCAG[-/A]AAAAAAAAAAAAGGA | 9100 |
rs113929414 | snp | A/C/G | 0.00557542 | 0.0525036 | intron-variant | USP10 | GRCh38.p7 | 16:84775532 | TGACCTCTCCCGGCT[A/C/G]TGCTTGTGGCACCTG | 9100 |
rs113935486 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84749040 | TGTTTGTTGAGGCTT[C/T]GATAGACAGAACGTA | 9100 |
rs113994255 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | USP10 | GRCh38.p7 | 16:84743412 | GCACACTCACTTGCA[C/T]GTAACTGGCCCCTCT | 9100 |
rs114006022 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84732800 | AACTGGTAGGCACTT[G/T]CCAGACTCACATCCG | 9100 |
rs114012071 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | USP10 | GRCh38.p7 | 16:84710833 | GCAGGTCCCCAGGCC[A/G]TCTGAGCCAGGCTCA | 9100 |
rs114023582 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | USP10 | GRCh38.p7 | 16:84738202 | CATTCTCTCTTCCCC[A/G]AGCAGAACAGAATAC | 9100 |
rs114060015 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP10 | GRCh38.p7 | 16:84743152 | ATAAATTCATTTCCC[C/T]TTGATATTCTTTTCA | 9100 |
rs114103644 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | USP10 | GRCh38.p7 | 16:84753578 | GTGATCTGCCGCACA[A/G]TGAATGAAGTGGCAG | 9100 |
rs114105583 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP10 | GRCh38.p7 | 16:84751339 | CCTAAAACTGATCTT[C/T]ATTTTGGCAGTTTAT | 9100 |
rs114183169 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | USP10 | GRCh38.p7 | 16:84774621 | GACTACAGCCGCGTG[C/T]CACCACGCCCGGGTA | 9100 |
rs114183359 | snp | A/T | 0.00597247 | 0.0543191 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779888 | AGGAGTATAAAGTTG[A/T]CGCCCATCAATAAAA | 9100 |
rs114189990 | snp | A/C | 0.0295035 | 0.117819 | intron-variant | USP10 | GRCh38.p7 | 16:84712665 | GAGCTGATGAAGAAG[A/C]GGTGGCTGCTTCCCA | 9100 |
rs114192901 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | USP10 | GRCh38.p7 | 16:84727140 | TTCTTTGAAATTACA[A/G]GAAACGATGAACTTA | 9100 |
rs114244106 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | USP10 | GRCh38.p7 | 16:84777283 | TGCAGTCCCCCTTGA[A/C]ATTTTAGAATGGAGA | 9100 |
rs114306977 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | USP10 | GRCh38.p7 | 16:84775809 | GCTTAGGCTCCCTGC[A/G]GTATCATTTTTTCTG | 9100 |
rs114315049 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | USP10 | GRCh38.p7 | 16:84739839 | TTATAGTGCGCTTTC[C/T]TCTGCTCTCCGACCA | 9100 |
rs114315095 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | USP10 | GRCh38.p7 | 16:84750596 | ATGCTTTCATTGAAC[A/G]TTGTACTTTTCCTGG | 9100 |
rs114370530 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | USP10 | GRCh38.p7 | 16:84734218 | ATCTAGGATTTTAAC[A/G]GTCTTCATTCCCATC | 9100 |
rs114371769 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | USP10 | GRCh38.p7 | 16:84739012 | TCTTTTGTTCTGCCC[C/T]CAGGTAGCAGTTTAT | 9100 |
rs114391759 | snp | A/T | 0.0260105 | 0.111035 | intron-variant | USP10 | GRCh38.p7 | 16:84704634 | GGGGTATGTGTATAG[A/T]ATTTGTTTCAAGGAT | 9100 |
rs114449689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84707103 | TTGAGGTCAAATGGC[C/T]GCTGGCCATCAGGAC | 9100 |
rs114452686 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | USP10 | GRCh38.p7 | 16:84722257 | TTTAGATTTAGCCAT[A/G]TTGAGTGTTGAGTTC | 9100 |
rs114482532 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | USP10 | GRCh38.p7 | 16:84701057 | TCATTGTGTATTTGT[A/G]TTAAATATGGGGAAA | 9100 |
rs114494840 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84776314 | GAGGGCCTAGCGGTG[A/G]GGGCCCAGGGGTGAG | 9100 |
rs114523718 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | USP10 | GRCh38.p7 | 16:84706128 | CTCAAGGGATCCCTT[C/T]TGCTTCAGCTTCCTA | 9100 |
rs114574349 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | USP10 | GRCh38.p7 | 16:84758335 | AGTGTCTGAGGCGCC[C/T]TGCTGCTGATGAGAC | 9100 |
rs114576342 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | USP10 | GRCh38.p7 | 16:84768692 | TTATTTATGTTCATG[A/G]TACCGTAGGGTACAA | 9100 |
rs114592763 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | USP10 | GRCh38.p7 | 16:84746155 | ATACACCAAGGTCAG[C/G]TCTTGAAGAGAAAAA | 9100 |
rs114605464 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | USP10 | GRCh38.p7 | 16:84763457 | TATATACATACATAC[A/G]CATACATTTTCCCTG | 9100 |
rs114607677 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | USP10 | GRCh38.p7 | 16:84737837 | GGCACACCCTGAGTG[C/G]CCAGTCAGTGCCACC | 9100 |
rs114675553 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | USP10 | GRCh38.p7 | 16:84738217 | GAGCAGAACAGAATA[C/T]TGGGAAGTGTGAAGA | 9100 |
rs114675616 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84754037 | GGCCACCAAGTCCTG[C/T]TACCTTAGATGGTGC | 9100 |
rs114677057 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | USP10 | GRCh38.p7 | 16:84766403 | CCACTGTCTGTGGTT[C/T]CTTGGGACACGTCGT | 9100 |
rs114686537 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | USP10 | GRCh38.p7 | 16:84761659 | CTGGTCCCATAGGTA[A/C]CATCTGCCTGGCTTG | 9100 |
rs114692598 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | USP10 | GRCh38.p7 | 16:84742715 | GCCATGCGGTGCAAG[A/G]CACATGGCGTCCATT | 9100 |
rs114698264 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP10 | GRCh38.p7 | 16:84743353 | GATTCTAAAGCATAC[A/G]AAGATTCAGGAGGCC | 9100 |
rs114699874 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | USP10 | GRCh38.p7 | 16:84755265 | CTTCGCCCTAACTCT[A/G]CCCTAGAAGACCTTT | 9100 |
rs114772935 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | USP10 | GRCh38.p7 | 16:84730030 | ATTTCTGTTGTGTTT[A/G]CTTTTTATGATTAAT | 9100 |
rs114776898 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84700860 | CTCTTTTTGGGAGAT[A/G]TGCGTGTAGAGTTAA | 9100 |
rs114797475 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | USP10 | GRCh38.p7 | 16:84751398 | TTGGGGGAAATGGTT[G/T]CTCAGATATTTTGCA | 9100 |
rs114818635 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | USP10 | GRCh38.p7 | 16:84737743 | GAAGCTGGCAGTGTC[A/G]CCTGGCTTCCTCATC | 9100 |
rs114833485 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84739786 | AGTTAATTAAGGCAC[C/T]GTGTTAAAAAGGGAG | 9100 |
rs114912889 | snp | C/G | 0.0287284 | 0.116357 | intron-variant | USP10 | GRCh38.p7 | 16:84714040 | CTAGAAAGGCTTTTC[C/G]TGGGCACCAGAATAG | 9100 |
rs114977231 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84736228 | CTAGTCGAATTTTTC[A/C/G]TATGCTTTTTCTCCG | 9100 |
rs114977897 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84766572 | CTCAAATGGAGGCAT[C/T]GGGAACATGGTTTTT | 9100 |
rs114984943 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | USP10 | GRCh38.p7 | 16:84747920 | TTGCAAGGACTGATA[A/C]TGTAGGTGGATGACA | 9100 |
rs115065800 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | USP10 | GRCh38.p7 | 16:84742737 | GCGTCCATTGTGAGT[C/G]TTCCTCCATAAGAAG | 9100 |
rs115074717 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP10 | GRCh38.p7 | 16:84704126 | GTGGTATCATCTCCA[A/G]TTGAATTAGTTACAT | 9100 |
rs115074831 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | USP10 | GRCh38.p7 | 16:84729322 | AAAATGTGCATTGCA[A/T]TTCTAAGAAATTCCG | 9100 |
rs115078357 | snp | C/G | 0.00164218 | 0.0286076 | intron-variant | USP10 | GRCh38.p7 | 16:84733137 | GCAGTATTTGTGAAC[C/G]AATAAAAATCTCCTG | 9100 |
rs115162073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718242 | AGAAGACATTTCTGA[A/G]GAGTTGCTTGTGAGT | 9100 |
rs115166719 | snp | G/T | 0.0146672 | 0.084371 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719854 | TGGAGGGCATGTTTC[G/T]ACAGATCATTAGGTG | 9100 |
rs115172212 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | USP10 | GRCh38.p7 | 16:84712538 | ATTCACTGTTTTCAG[C/G]ACTGCTTATGGTTGT | 9100 |
rs115175475 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84758569 | TGATGTTGAACTGAA[G/T]GAAGCCTTAACAGTA | 9100 |
rs115184057 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | USP10 | GRCh38.p7 | 16:84737483 | TGTGAGGGAGGTTTG[C/G]TGAATGAAAGGTGCT | 9100 |
rs115226912 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | USP10 | GRCh38.p7 | 16:84701017 | CATCTGGTCCCTATA[A/G]ATTGTTGCACACTTT | 9100 |
rs115256415 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | USP10 | GRCh38.p7 | 16:84773628 | GCCGGGTTTAGTGTC[C/T]GTTGCTCCTCTCACA | 9100 |
rs115275914 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | USP10 | GRCh38.p7 | 16:84775717 | GGCCCTCAGTCAGTC[A/T]TGAGAAATCTCCCAA | 9100 |
rs115281405 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | USP10 | GRCh38.p7 | 16:84738386 | GGGGCATCCTAGTGT[C/T]ATTAACAGAAAAAGA | 9100 |
rs115288324 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | USP10 | GRCh38.p7 | 16:84712777 | TTTACCTCTGTTGTG[C/T]AGTTTCTTGAATCCA | 9100 |
rs115291981 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84739807 | AAAAAGGGAGCTGCA[G/T]TCACCAGGCTTTTTG | 9100 |
rs115296459 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | USP10 | GRCh38.p7 | 16:84714872 | TAATATCAAAAACAA[A/G]TTCTACATATGAAAT | 9100 |
rs115344722 | snp | A/G | 0.030278 | 0.119257 | intron-variant | USP10 | GRCh38.p7 | 16:84777349 | GGCCCTGCAGATTCT[A/G]CTGATGGTCGCTTTG | 9100 |
rs115350102 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | USP10 | GRCh38.p7 | 16:84777456 | TCCAGGGGACATGCT[A/G]CTGTCATGGGTGCTT | 9100 |
rs115620717 | snp | C/G | 0.00914312 | 0.0669923 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698882 | TTCCGGGTGTGAGCC[C/G]CTGCGCCTGGCCCAC | 9100 |
rs115622199 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | USP10 | GRCh38.p7 | 16:84778573 | CATGAGCCAGGTCTG[C/T]AGGCCTGTACAGCTG | 9100 |
rs115632781 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | USP10 | GRCh38.p7 | 16:84707445 | CGTATTTAAAGTGAA[A/T]AGTAGAAGTCATTCC | 9100 |
rs115637766 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | USP10 | GRCh38.p7 | 16:84732402 | AATCATTGCTTCTCC[A/G]TTGTGGAAATTGCTA | 9100 |
rs115650037 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | USP10 | GRCh38.p7 | 16:84728367 | TTTTTACTTTTTTTT[C/T]TTCTCGCTGTTGCCC | 9100 |
rs115667642 | snp | C/G | 0.0146672 | 0.084371 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719599 | GCTAGGTGAGTACCA[C/G]CGCGGATTGGTTACC | 9100 |
rs115682816 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | USP10 | GRCh38.p7 | 16:84710929 | CATGAATAGCAATAA[C/T]GAAATCGTATTTTGG | 9100 |
rs115692602 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717455 | CCAGTTCTTTGAAGG[C/T]AGGACACATTGCTTA | 9100 |
rs115742664 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | USP10 | GRCh38.p7 | 16:84729207 | TGATGTCTTAACCTT[C/T]ACATTTGTATGGATT | 9100 |
rs115752592 | snp | G/T | 0.0103295 | 0.0711199 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699553 | AGTGAACAAATGAAT[G/T]AATGCGCGGCAACGG | 9100 |
rs115809444 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | USP10 | GRCh38.p7 | 16:84704381 | GCAAGAATCACCATC[A/G]CACAAAACAGATAAA | 9100 |
rs115844061 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | USP10 | GRCh38.p7 | 16:84759255 | TCTAAGTAGTTCAAC[A/G]TCCTTAGCTTCCTTG | 9100 |
rs115846298 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | USP10 | GRCh38.p7 | 16:84771595 | AATACTAGGCCTAGC[A/G]TGGTGGCTCACGCCT | 9100 |
rs115861686 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719674 | AAACATCTCTTCTAG[A/T]GTATGTAGGTCCCAT | 9100 |
rs115881577 | snp | A/G | 0.00621288 | 0.0553881 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745437 | CAACCAAACCCGAGA[A/G]TGCATCACCTCCTGC | 9100 |
rs115975726 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717338 | TCCCTTTTAGAAATT[C/T]TGTGCAGATTAAATG | 9100 |
rs116025941 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | USP10 | GRCh38.p7 | 16:84730920 | TTCTGAAGTAAAAGG[A/C]CTTTCTTGTTAGTCA | 9100 |
rs116044132 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84734808 | TAAGCTGAAATTGAG[A/G]CACTGAATTTTGTAT | 9100 |
rs116072959 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | USP10 | GRCh38.p7 | 16:84775942 | CTGTTTGCCGCACTT[C/T]TGTTTGCTTCCCAGG | 9100 |
rs116084310 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | USP10 | GRCh38.p7 | 16:84756854 | TATGGTTTAAAGACA[A/G]ATGTAAAAATCCACT | 9100 |
rs116094419 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | USP10 | GRCh38.p7 | 16:84746132 | AATGGATTTTATTCA[C/G]AATTTTGATACACCA | 9100 |
rs116132888 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | USP10 | GRCh38.p7 | 16:84749317 | CAGCGTTTAACTGAG[C/T]GAAAGTCTAGTTTCA | 9100 |
rs116156397 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | USP10 | GRCh38.p7 | 16:84778761 | TGGTTTGTGTGATGA[A/C]ATCTCTCTGTCCCAC | 9100 |
rs116168850 | snp | A/C | 0.0271762 | 0.113356 | intron-variant | USP10 | GRCh38.p7 | 16:84715631 | TTATGTGTTAGGGTG[A/C]CCTCCCTTTTTTTTT | 9100 |
rs116219221 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84705123 | TAGCTGGAGGGACAT[C/G]TCCTTAAGCCTGTAC | 9100 |
rs116255115 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | USP10 | GRCh38.p7 | 16:84769775 | ACCCTTTTGTGATGT[C/G]TCTGTTTTTCTCTTT | 9100 |
rs116256015 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | USP10 | GRCh38.p7 | 16:84716721 | GGGATCTTAGGTGCA[C/T]GACCTTCGGCAAGGT | 9100 |
rs116276921 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | USP10 | GRCh38.p7 | 16:84744035 | GAAGTGCGCTTTTAT[A/C]TATAGGATTCTTTGT | 9100 |
rs116277251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84724765 | TTACTCTCGTAGTCT[C/T]GCATAGTTGAGTGTG | 9100 |
rs116302310 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | USP10 | GRCh38.p7 | 16:84777382 | GCAAAACTCTTAGCC[C/T]AGTCAGTTAGGTCTG | 9100 |
rs116360189 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | USP10 | GRCh38.p7 | 16:84746752 | CTTAGGCTGTACTAC[A/G]TTGATTTACAAATTT | 9100 |
rs116372305 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | USP10 | GRCh38.p7 | 16:84741298 | CAGATCTAACAATAG[C/T]TTAGGACAAGTAATA | 9100 |
rs116392963 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | USP10 | GRCh38.p7 | 16:84751156 | GTTGCCTACGGTATT[C/G]AGTACACAACATGCT | 9100 |
rs116443686 | snp | C/G | 0.0271762 | 0.113356 | intron-variant | USP10 | GRCh38.p7 | 16:84770454 | CTATATAGAAAATGT[C/G]TGCCTTTGTTGAGTG | 9100 |
rs116476938 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | USP10 | GRCh38.p7 | 16:84735671 | ATGGTAAGTTATGCC[A/C]AACCTTTTATTCACA | 9100 |
rs116479287 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | USP10 | GRCh38.p7 | 16:84759613 | AAATAGACTGTTGGC[G/T]ATTTTATATGGAAGT | 9100 |
rs116479567 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | USP10 | GRCh38.p7 | 16:84707298 | GAAACTTTAATGTTA[C/G]TAATTACAAAATTTG | 9100 |
rs116483394 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | USP10 | GRCh38.p7 | 16:84769605 | TGACTGTCGGCTTGG[C/T]TCACTTCTGTGGCAG | 9100 |
rs116502067 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | USP10 | GRCh38.p7 | 16:84742077 | TGTGTTTTTTAATTT[C/T]TTTATATTTTAATTT | 9100 |
rs116526806 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | USP10 | GRCh38.p7 | 16:84775935 | ATTGTTGCTGTTTGC[C/T]GCACTTTTGTTTGCT | 9100 |
rs116535998 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | USP10 | GRCh38.p7 | 16:84730579 | TGACTTGAGGGTGTT[C/T]GCCGCTGACTCATGC | 9100 |
rs116566572 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84708551 | TTATTAGTTGGAGAT[A/T]GGTAAGTCACCTGCC | 9100 |
rs116585406 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | USP10 | GRCh38.p7 | 16:84747261 | CTTTCTGTAATACTT[G/T]CTGATGTGACCTTTT | 9100 |
rs116618850 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | USP10 | GRCh38.p7 | 16:84731668 | TTGCCCCATTGCCTT[A/C]CATAGCCTTGTTGAT | 9100 |
rs116648135 | snp | C/G | 0.0055519 | 0.0523939 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84760191 | TGGAGATAAAATCGT[C/G]AGGGATATTCGCCCT | 9100 |
rs116668798 | snp | A/T | 0.0256215 | 0.110247 | intron-variant | USP10 | GRCh38.p7 | 16:84748858 | ACTGGTAGTAGAGGA[A/T]AGCCTTGCCACACAC | 9100 |
rs116704962 | snp | G/T | 0.0264193 | 0.111988 | intron-variant | USP10 | GRCh38.p7 | 16:84704157 | CAGGGTTTTTGTTTC[G/T]GTTTTTTGTTTGTTT | 9100 |
rs116706181 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | USP10 | GRCh38.p7 | 16:84708118 | TTGAAGACTTCCACC[C/G]CCTTAGTAGTAGTCA | 9100 |
rs116714164 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | USP10 | GRCh38.p7 | 16:84775386 | AGAGTTTTACCTGAA[A/G]CTCTGCGTAGATGAC | 9100 |
rs116730152 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | USP10 | GRCh38.p7 | 16:84761620 | GGTCATTACAGACTC[C/T]GTGTCCAGAGTTTTT | 9100 |
rs116733207 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | USP10 | GRCh38.p7 | 16:84712539 | TTCACTGTTTTCAGG[A/G]CTGCTTATGGTTGTT | 9100 |
rs116759886 | snp | G/T | 0.0448719 | 0.142907 | intron-variant | USP10 | GRCh38.p7 | 16:84724864 | AGTGTCATCTCCAGA[G/T]GTCCTCAGAACCACC | 9100 |
rs116793039 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | USP10 | GRCh38.p7 | 16:84713288 | CCCTCTGTCTGTAGA[C/T]AGGCTCGCCCCCTTT | 9100 |
rs116910794 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | USP10 | GRCh38.p7 | 16:84750488 | TGTTAAGAGTGAGTA[C/T]GGCAGACACGTGGGG | 9100 |
rs116913314 | snp | C/T | 0.0287555 | 0.11658 | intron-variant | USP10 | GRCh38.p7 | 16:84716664 | AGGGAGCTGCCTGCA[C/T]GAAGGCTGATCAGCA | 9100 |
rs116919724 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | USP10 | GRCh38.p7 | 16:84730607 | TGCTGAAGCCACTTG[G/T]TGTCTGCGTTTGAAA | 9100 |
rs116946301 | snp | G/T | 0.0402882 | 0.136092 | intron-variant | USP10 | GRCh38.p7 | 16:84738280 | GACTCAGAAAAAGAT[G/T]ATTTCTTGATGTTAC | 9100 |
rs116959882 | snp | A/G | 0.00310164 | 0.0392581 | intron-variant | USP10 | GRCh38.p7 | 16:84759475 | TGATAGACAGCTTGT[A/G]AGTAAGGTGGTGAAA | 9100 |
rs116961138 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718101 | ACTTGACTACATTGC[A/G]AAGGGAAAATCTTGG | 9100 |
rs116971229 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | USP10 | GRCh38.p7 | 16:84738868 | ATCAAGCAGCAGCTC[C/T]CATACAGTATTGGGC | 9100 |
rs117002428 | snp | A/G | 0.000503119 | 0.0158527 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764120 | CCCCAAAAACCACTC[A/G]GTCAATGAAGAAGAG | 9100 |
rs117117273 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | USP10 | GRCh38.p7 | 16:84749380 | GTTTGACTTGCATTA[A/G]TATCTAACTGTTTCT | 9100 |
rs117153286 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84754279 | TTTTAGTTTATGAAA[C/G]ACTTGCCACTAGATA | 9100 |
rs117186215 | snp | A/G/T | 0.00417235 | 0.0454872 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779116 | GTGCGCCCAGTGCCC[A/G/T]CTTCGTAGGACACCA | 9100 |
rs117190488 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84756998 | GGTGGACCCAGGTTC[A/C]CAGGTCATTTCAGCT | 9100 |
rs117245476 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | USP10 | GRCh38.p7 | 16:84704994 | ACCTGCTACCGTCTG[C/T]GCTGTAATGGTGGCT | 9100 |
rs117255588 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84772468 | GAGGACGTCTTTGAG[C/T]GGAAGGTGGATGTGG | 9100 |
rs117272162 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779841 | TCTTCTCTAATGCTG[C/T]GTCCCTAATTGTACA | 9100 |
rs117346875 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | USP10 | GRCh38.p7 | 16:84759176 | GCTTCGTAGATCCTT[A/G]TATGGACATCACAGG | 9100 |
rs117403363 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84724042 | TTCTACTAGGGCTAT[C/G]CCAGATAAAGTTGAC | 9100 |
rs117405502 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | USP10 | GRCh38.p7 | 16:84770177 | AAGATAAAAAGGATG[C/T]TGCCAGCCGTTCTGG | 9100 |
rs117412146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84739916 | GTGAATAAGAGGTGC[A/G]GTCAGGAAGAGTCAT | 9100 |
rs117472516 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84757803 | ATCACAGGTGAGTTA[A/G]TCAGTCTTTGGGAGC | 9100 |
rs117520594 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84729820 | GGAGTTCAAAACAGC[A/C]GTGGCTAGTGATTTG | 9100 |
rs117522014 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | USP10 | GRCh38.p7 | 16:84757672 | GTTGGTACATAGTAG[A/G]TGTATCTATTTGTGG | 9100 |
rs117523331 | snp | A/T | 0.046775 | 0.145601 | intron-variant | USP10 | GRCh38.p7 | 16:84777035 | CCAGGCTGGAAGCCT[A/T]TTCTGATCTTGGAAA | 9100 |
rs117643976 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84738809 | GCTGTGATTATTGAA[G/T]TGGTGTGCTGAGATC | 9100 |
rs117693224 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84727531 | AACTTGAAAAGTTGC[A/G]GAAAGAAAAATAGTA | 9100 |
rs117756079 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84766579 | GGAGGCATCGGGAAC[A/T]TGGTTTTTGTGCAGA | 9100 |
rs117776868 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | USP10 | GRCh38.p7 | 16:84707613 | TTGTTTTCAAAATTA[C/T]TGAAAACATCCACTG | 9100 |
rs117879661 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | USP10 | GRCh38.p7 | 16:84774926 | GAGCATCACAGCCTC[A/G]GCCGTTGCTCCTGTT | 9100 |
rs117880120 | snp | C/T | 0.00558353 | 0.0525413 | intron-variant | USP10 | GRCh38.p7 | 16:84778880 | CACTCTGCTGCCTGC[C/T]GGGCTCTCTTCCAGT | 9100 |
rs117907709 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | USP10 | GRCh38.p7 | 16:84729573 | GGAAATTCTAATCAA[C/G]TTCCCCGGGAGGCTG | 9100 |
rs117919441 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84704115 | AATTGAGAAAAGTGG[A/T]ATCATCTCCAATTGA | 9100 |
rs117935640 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718207 | GATGAGTTTAATTAC[A/G]AAAGAAATGTCTTTT | 9100 |
rs117941836 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717261 | TCTTTAGGGGGTGGG[A/C]CTAATTCCCTTACAT | 9100 |
rs117985202 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84723699 | AGATGGATCTAACTC[A/G]ATTCTTGTACTTTAA | 9100 |