| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs2951100 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139059 | TATATGTGCCTATCA[C/G]CCTGAGGAGTAATTT | 377630 |
| rs3988859 | snp | C/T | 1.89564e-05 | 0.00307861 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138555 | CCAGGAAGAAGCTTC[C/T]TCTGAGTAGCAGGAG | 377630 |
| rs3988860 | snp | A/T | 3.88191e-05 | 0.00440546 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138489 | GAAATACCTGCTACG[A/T]GAACGCTTCCCTGCA | 377630 |
| rs3988861 | snp | C/T | 1.94256e-05 | 0.00311647 | USP17L2, FAM66D | 8 | allele_origin=T(somatic)/C(germline) | 8:12138478 | TACGAGAACGCTTCC[C/T]TGCAGTGCCTGACAT | 377630 |
| rs3988862 | snp | A/G | 4.89848e-05 | 0.00494874 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138413 | GGAGCACTCTCAAAC[A/G]TGTCAGCGTCCCAAG | 377630 |
| rs3988863 | snp | G/T | 0.000247127 | 0.0111132 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138407 | CTCTCAAACATGTCA[G/T]CGTCCCAAGTGCTGC | 377630 |
| rs3988864 | snp | A/C | | | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138402 | AAACATGTCAGCGTC[A/C]CAAGTGCTGCATGCT | 377630 |
| rs3988865 | snp | C/G/T | 0.000162121 | 0.00900208 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138397 | TGTCAGCGTCCCAAG[C/G/T]GCTGCATGCTCTGTA | 377630 |
| rs3988870 | snp | A/G | | | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138162 | AAATATTTGGAGGCT[A/G]CTGGAGATCTCAAAT | 377630 |
| rs3988871 | snp | C/G | | | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138125 | TCTCCACTGCCACGG[C/G]ATTTCAGACACTTTT | 377630 |
| rs3988872 | snp | A/C | | | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138061 | GCAGCTCAGAGTGTC[A/C]AGCAAGCTTTGGAAC | 377630 |
| rs4841752 | snp | G/T | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139797 | CTTTTGTTTATTAAA[G/T]AACTGATGAAAATAA | 377630 |
| rs4841753 | snp | C/G | 0.401392 | 0.198948 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139836 | TATCTCACAGCATGG[C/G]TGATACTATTTCCAT | 377630 |
| rs4841754 | snp | C/T | 0.370772 | 0.218893 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140046 | CTTTTTAATACTGGC[C/T]CTTGTTTCACTGGGA | 377630 |
| rs4841755 | snp | C/G | 0.352938 | 0.227824 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140060 | CTCTTGTTTCACTGG[C/G]AAATGGCAAAAATAA | 377630 |
| rs4841756 | snp | A/G | 0.366679 | 0.221102 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140201 | ATTGTAATGCTGACG[A/G]AAGTGGACATGTTCC | 377630 |
| rs9693024 | snp | A/G | 0.197531 | 0.244432 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140103 | CTGGATTCTCGCATC[A/G]GTTGTTCATGCTCTG | 377630 |
| rs9693093 | snp | C/T | 0.473266 | 0.112482 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140047 | TTTTTAATACTGGCT[C/T]TTGTTTCACTGGGAA | 377630 |
| rs9693300 | snp | A/G | 0.475789 | 0.107327 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140486 | TCATGGGCCAGGTGT[A/G]CTTCATCAGAAGGCT | 377630 |
| rs9693352 | snp | C/T | 0.457154 | 0.139954 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140170 | TGGAATTGCAGTTAG[C/T]ACCTTTGATGCAAAA | 377630 |
| rs9693390 | snp | C/T | 0.499776 | 0.0105807 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140511 | AAGGCTTCCTATGCC[C/T]GATGTAAAGTGTCCT | 377630 |
| rs9694549 | snp | A/G | 0.457154 | 0.139954 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140178 | CAGTTAGCACCTTTG[A/G]TGCAAAAATTGTAAT | 377630 |
| rs9774478 | snp | C/G | 0.000172898 | 0.00929619 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137966 | GTGTAAAGTTAACGT[C/G]TTGGAGGCCGGCGCC | 377630 |
| rs10090565 | snp | A/G | 0.195837 | 0.244062 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140019 | AGTGAGTGAAACAGA[A/G]GGTAGCATAACCTTT | 377630 |
| rs10090570 | snp | A/G | 0.195837 | 0.244062 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140021 | TGAGTGAAACAGAGG[A/G]TAGCATAACCTTTTT | 377630 |
| rs11250189 | snp | A/G | 0 | 0 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139560 | GTAGAAACATGCACT[A/G]AAGTTTGAAGAGTTA | 377630 |
| rs11250190 | snp | A/T | 0.0263992 | 0.111815 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139573 | CTGAAGTTTGAAGAG[A/T]TACTCAGTGCACAAA | 377630 |
| rs11777425 | snp | C/T | 0.488363 | 0.0753851 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136926 | GTCTCTCCAGAGGTT[C/T]GGAAGACTCACGACC | 377630 |
| rs11990104 | snp | G/T | 0.32955 | 0.237006 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139386 | TAATAATAAAGGAGA[G/T]ATCCGTGGCATCAAA | 377630 |
| rs11992686 | snp | A/G | 0.476401 | 0.106032 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139716 | AGTGGTTTCGGACGT[A/G]CGGCGGCAGTTTAAG | 377630 |
| rs12543578 | snp | C/T | 0.496123 | 0.0438589 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137448 | TGCTCTTGGGGGAAT[C/T]TCCAGTGGTCTAAGG | 377630 |
| rs12547403 | snp | A/G | 0.46865 | 0.121211 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140742 | TGATGTCCTGCCTGC[A/G]TGTCATGCTCATTGC | 377630 |
| rs12677320 | snp | A/G | 0.449091 | 0.151204 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139832 | AACGTATCTCACAGC[A/G]TGGGTGATACTATTT | 377630 |
| rs12677836 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140048 | TTTTAATACTGGCTT[C/T]TGTTTCACTGGGAAA | 377630 |
| rs13274255 | snp | A/G | 0.369398 | 0.219645 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137765 | AGAGAAGTAATGTCC[A/G]TCGTGACAACTCCAC | 377630 |
| rs28396114 | snp | A/C | 0.0387552 | 0.1337 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139385 | TTAATAATAAAGGAG[A/C]TATCCGTGGCATCAA | 377630 |
| rs28488512 | snp | A/G | 0.489665 | 0.0711382 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139284 | CGTCATCCTCTCATC[A/G]ACGGAAGGACAAGAA | 377630 |
| rs28491134 | snp | A/C/G/T | 0.100281 | 0.204129 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138801 | TTTTTCTGCTGGGAC[A/C/G/T]GCAGGTTGCAGCAAG | 377630 |
| rs28569037 | snp | A/C | 0.0869089 | 0.189476 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139811 | AGAACTGATGAAAAT[A/C]AAAACAACGTATCTC | 377630 |
| rs28580271 | snp | A/C | 0.489434 | 0.0719116 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139395 | AGGAGATATCCGTGG[A/C]ATCAAACAGACCTTC | 377630 |
| rs28653124 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139182 | TGTGTGTATCTCTCT[C/G]TGTGTGTGTGTGTGT | 377630 |
| rs34009999 | in-del | -/C | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139924 | CTACGGTATAATTTT[-/C]CCTTGTTTGCTTTTG | 377630 |
| rs34648338 | in-del | -/C | | | frameshift-variant, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137330 | GTGTGGGATGAAAAA[-/C]CCATCATCCTGAACA | 377630 |
| rs36114754 | snp | G/T | 0.457154 | 0.139954 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140173 | AATTTTTGCATCAAA[G/T]GTGCTAACTGCAATT | 377630 |
| rs55731049 | snp | G/T | 0.0908922 | 0.192833 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140098 | ATCTCCTGGATTCTC[G/T]CATCGGTTGTTCATG | 377630 |
| rs55769296 | snp | A/G | 0.0908922 | 0.192833 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140076 | AAATGGCAAAAATAA[A/G]CCGTGTATCTCCTGG | 377630 |
| rs56021150 | in-del | -/CT | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139175 | TGTGTGTATCTCTCT[-/CT]GTGTGTGTGTGTGTG | 377630 |
| rs56335315 | snp | G/T | 0.378174 | 0.214642 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136762 | TCACCTTCTCGTGCC[G/T]CCCAACAACTGACGA | 377630 |
| rs62493707 | snp | C/G/T | 7.80792e-05 | 0.00624768 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137995 | CCCTCTGGAGACAAA[C/G/T]ACCGCAATGATAGGC | 377630 |
| rs62493708 | snp | A/G | 0.00281957 | 0.0374411 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137999 | CTGGAGACAAAGACC[A/G]CAATGATAGGCATTC | 377630 |
| rs71237667 | snp | C/T | 0.148284 | 0.228407 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138743 | GGAGGACGACTCACT[C/T]TACTTGGGAGGTGAG | 377630 |
| rs73544419 | snp | C/T | 0.0490535 | 0.14873 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140295 | TCCTGGCTCTAGGGA[C/T]TTTCCCAAAATGTCT | 377630 |
| rs73663091 | snp | A/C | 0 | 0 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139868 | CTTACGTGATAATGG[A/C]TCAACATTTCATAGA | 377630 |
| rs74324142 | snp | C/G | 0.387647 | 0.208695 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138641 | AGATGAGAGTGGTGA[C/G]TTCTCAGGGAGAGAA | 377630 |
| rs74515408 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138877 | CGCATCAGCCCTTAT[A/G]TAACTCACCCCCACC | 377630 |
| rs74605293 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139225 | GTGTGTGTGTGTGTG[C/T]TTGTGCTGGGATGAA | 377630 |
| rs74614551 | snp | C/T | 0.498602 | 0.0270118 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137975 | TAACGTCTTGGAGGC[C/T]GGCGCCCTCTGGAGA | 377630 |
| rs74683378 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139907 | AAAAAGTTCTAATTT[G/T]GACAAAAGCAAACAA | 377630 |
| rs75173287 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139857 | CTATTTCCATACTTA[C/T]GTGATAATGGATCAA | 377630 |
| rs75180221 | snp | C/G/T | 0.000191701 | 0.0097886 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137924 | GGAGAATCTCTTCAA[C/G/T]ACAAGGATGAGGACC | 377630 |
| rs75476700 | snp | A/G | 0.382899 | 0.21175 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138577 | TCTTCCTGGGAGCAA[A/G]CTGTCTTGCCACAGG | 377630 |
| rs75554685 | snp | A/G | 0.168785 | 0.236441 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140684 | CGGGACCTAGGAATT[A/G]TTGTCCTTTAATGCT | 377630 |
| rs75807755 | snp | A/G | 0.379999 | 0.213542 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137553 | AGCTCTCCTTGCGTT[A/G]CTCGCCTGTCTGTGT | 377630 |
| rs75937106 | snp | A/G/T | 0.010092 | 0.0703645 | missense, synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138752 | CAAGTAGAGTGAGTC[A/G/T]TCCTCCATGTCGCCC | 377630 |
| rs75952964 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139851 | GTGATACTATTTCCA[C/T]ACTTACGTGATAATG | 377630 |
| rs76189682 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139370 | AGCGTATTTTCTTCC[C/T]TAATAATAAAGGAGA | 377630 |
| rs76415856 | snp | C/T | | | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137377 | GAATCACAAGTACGT[C/T]GGGAGGCAGGGTACC | 377630 |
| rs76662498 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138875 | GCCGCATCAGCCCTT[A/C]TATAACTCACCCCCA | 377630 |
| rs76753250 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139647 | GACTAATTGATGACA[A/T]TCCCCAAATTTATGT | 377630 |
| rs76814845 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139800 | TTGTTTATTAAAGAA[C/T]TGATGAAAATAAAAA | 377630 |
| rs77973456 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138813 | GACTGCAGGTTGCAG[A/C]AAGACGCTATCTCTT | 377630 |
| rs78280428 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138881 | TCAGCCCTTATATAA[C/T]TCACCCCCACCAACC | 377630 |
| rs78425152 | snp | C/T | | | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136966 | GATGTTTCCCATGTG[C/T]GGGCTCATCCTGAGA | 377630 |
| rs78927706 | snp | A/G | | | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136963 | CTTGATGTTTCCCAT[A/G]TGTGGGCTCATCCTG | 377630 |
| rs79412221 | snp | C/T | | | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137098 | GTGTTTGCGTGCGCG[C/T]TTGTGGGTGTATTTG | 377630 |
| rs79865132 | snp | C/G | 0.0246802 | 0.10831 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138578 | CTTCCTGGGAGCAAG[C/G]TGTCTTGCCACAGGA | 377630 |
| rs111428074 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140316 | CAAAATGTCTTAGAC[A/G]GTAAGGAACAGGGCA | 377630 |
| rs111978476 | snp | A/G | 0.0700422 | 0.173537 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139665 | CCCAAATTTATGTGT[A/G]CCAGAAAAGAGAGAT | 377630 |
| rs112165118 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140020 | GTGAGTGAAACAGAG[A/G]GTAGCATAACCTTTT | 377630 |
| rs112388014 | snp | A/C | 0.5 | 0 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140680 | TAAGCGGGACCTAGG[A/C]ATTGTTGTCCTTTAA | 377630 |
| rs112595287 | snp | A/G | | | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138152 | GAGACACTTGATTTG[A/G]GATCTCCAGCAGCCT | 377630 |
| rs112598423 | snp | A/G | 0.040671 | 0.13668 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139593 | CAGTGCACAAAGTAG[A/G]CTGTGAAAGACTTTG | 377630 |
| rs112856432 | snp | A/C | 0.5 | 0 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139435 | CCTTTCCACGTTCAG[A/C]CTATTGACTCTCTAT | 377630 |
| rs113086230 | snp | A/C | 0.5 | 0 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140304 | TAGGGATTTTCCCAA[A/C]ATGTCTTAGACAGTA | 377630 |
| rs113108697 | snp | C/G | 3.66441e-05 | 0.00428027 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138424 | GACATGTTTGAGAGT[C/G]CTCCCGGGACAGCAT | 377630 |
| rs113179798 | snp | A/G | 0.0887219 | 0.191022 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140024 | GTGAAACAGAGGGTA[A/G]CATAACCTTTTTAAT | 377630 |
| rs113890166 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139737 | GCAGTTTAAGAAAAC[A/T]TGAAACAAAAAACTT | 377630 |
| rs114424692 | snp | C/G | 0.0168055 | 0.0901129 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140715 | CATAACTGCTTTTGA[C/G]GTGAGCCGAATTGAT | 377630 |
| rs114758845 | snp | G/T | 0.197393 | 0.244402 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140006 | GACGTTTAAAAGCAG[G/T]GAGTGAAACAGAGGG | 377630 |
| rs115345095 | snp | C/T | 0.0193772 | 0.0965046 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140741 | TTGATGTCCTGCCTG[C/T]GTGTCATGCTCATTG | 377630 |
| rs139278194 | snp | C/T | | | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137013 | CAGTTGTCCCTGTTG[C/T]AGAGACAGAAACTTG | 377630 |
| rs140228481 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139920 | TTTGACAAAAGCAAA[C/G]AAGGAAAATTATACC | 377630 |
| rs140365730 | snp | C/T | 0.000607517 | 0.0174181 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137493 | GCTCTTTCCACCAAG[C/T]GCTCGTCCAACTCGG | 377630 |
| rs141763286 | snp | C/T | 0.364817 | 0.222075 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139120 | CACACAGTTGCCTTA[C/T]TTTAGGTAAAAGAAT | 377630 |
| rs142023572 | snp | C/T | 0.000207506 | 0.0101838 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138565 | TCAGAGGAAGCTTCT[C/T]CCTGGGAGCAAGCTG | 377630 |
| rs142415653 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140395 | GCTTCATGGCCCATG[A/G]AATTAGGATGATTTT | 377630 |
| rs143342329 | snp | C/T | | | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136691 | CTAAATGCATTCCAG[C/T]TTCCACTATTCAAGG | 377630 |
| rs143497277 | in-del | -/TC | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139174 | GAAACCGTGTGTGTA[-/TC]TCTCTCTGTGTGTGT | 377630 |
| rs144549165 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140499 | GTGCTTCATCAGAAG[G/T]CTTCCTATGCCCGAT | 377630 |
| rs147997361 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139994 | GAAAACATCGGAGAC[A/G]TTTAAAAGCAGTGAG | 377630 |
| rs149971640 | snp | A/C | 0.0383715 | 0.133092 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140342 | GAGGCCTTGGCGCCG[A/C]GCCTCAATTCTGCCC | 377630 |
| rs149988484 | snp | A/G/T | 0.0100832 | 0.0702856 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137507 | GCGCTCGTCCAACTC[A/G/T]GGTGCCTGGAGGCAG | 377630 |
| rs150740409 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139749 | AACTTGAAACAAAAA[A/C]CTTGAGAAATCCAAA | 377630 |
| rs151245022 | snp | C/T | | | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138286 | ATTCATGGGCATCTT[C/T]CTGCTTGCCTCTATG | 377630 |
| rs151307501 | snp | C/G | 0.0341408 | 0.126114 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140478 | TTGTCTTTTCATGGG[C/G]CAGGTGTGCTTCATC | 377630 |
| rs180745912 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139819 | TGAAAATAAAAACAA[C/T]GTATCTCACAGCATG | 377630 |
| rs181023148 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137031 | AGACAGAAACTTGGA[C/T]TCCTCATTACTTTAT | 377630 |
| rs181309607 | snp | A/C | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140235 | AACTAAGAGGGACAG[A/C]ATTTGGGTGTGTCTT | 377630 |
| rs181515737 | snp | C/T | 0.012468 | 0.0779649 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137578 | CTGTGTCTTCAGCGC[C/T]GAGGGCTCTTGGTTC | 377630 |
| rs181712148 | snp | C/T | 0.00835141 | 0.0640778 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139960 | CCCGGGTGACGGGAG[C/T]GAGGCCCTGTCTGAA | 377630 |
| rs181995900 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139206 | TGTGTGTGTGTGTGT[G/T]TGTGTGTGTGTGTGT | 377630 |
| rs182124355 | snp | A/C | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140490 | GGGCCAGGTGTGCTT[A/C]ATCAGAAGGCTTCCT | 377630 |
| rs182148341 | snp | A/C | 0.000369269 | 0.013583 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137344 | GGTTTTTCATCCCAC[A/C]CTTGTATTTCGATTG | 377630 |
| rs184299601 | snp | C/T | 0.00478085 | 0.0486577 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137090 | GTGTGTGTGTGTTTG[C/T]GTGCGCGCTTGTGGG | 377630 |
| rs184705752 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139713 | GTGAGTGGTTTCGGA[C/T]GTGCGGCGGCAGTTT | 377630 |
| rs185007015 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139848 | TGGGTGATACTATTT[C/T]CATACTTACGTGATA | 377630 |
| rs185815620 | snp | C/T | 0.000125422 | 0.00791804 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137689 | GGACAGAAGTGATGC[C/T]ACAGGCAGTGACCTT | 377630 |
| rs186057541 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139993 | AGAAAACATCGGAGA[C/T]GTTTAAAAGCAGTGA | 377630 |
| rs186311075 | snp | C/T | 0.00492165 | 0.0493619 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137495 | TCTTTCCACCAAGCG[C/T]TCGTCCAACTCGGGT | 377630 |
| rs186364143 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140361 | CGCCAAGGCCTCTGG[C/G]TGTAAAGAAACAGCC | 377630 |
| rs186397728 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140498 | TGTGCTTCATCAGAA[G/T]GCTTCCTATGCCCGA | 377630 |
| rs187403172 | snp | A/T | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136718 | AAGGTGGCGAGAATG[A/T]TCCATGGATGTGCCA | 377630 |
| rs187602744 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138883 | AGCCCTTATATAACT[C/T]ACCCCCACCAACCGC | 377630 |
| rs187635302 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139361 | ATTTAGCACAGCGTA[G/T]TTTCTTCCTTAATAA | 377630 |
| rs188414901 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139625 | GGAAATCATGCAATC[A/C]CCGAGAGACTAATTG | 377630 |
| rs188454321 | snp | G/T | 0.00358779 | 0.0422022 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137003 | CATCACTATCCAGTT[G/T]TCCCTGTTGTAGAGA | 377630 |
| rs189221289 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139714 | TGAGTGGTTTCGGAC[A/G]TGCGGCGGCAGTTTA | 377630 |
| rs189384808 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139935 | CAAGGAAAATTATAC[C/T]GTAGAAAAGCCCGGG | 377630 |
| rs190033976 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140078 | ATGGCAAAAATAAAC[C/T]GTGTATCTCCTGGAT | 377630 |
| rs190706999 | snp | C/T | 0.000245977 | 0.0110873 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137577 | TCTGTGTCTTCAGCG[C/T]CGAGGGCTCTTGGTT | 377630 |
| rs190811800 | snp | C/T | 0.00296897 | 0.0384144 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137334 | TCAGGATGATGGTTT[C/T]TCATCCCACACTTGT | 377630 |
| rs190848023 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140698 | TGTTGTCCTTTAATG[C/T]TCATAACTGCTTTTG | 377630 |
| rs190860830 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140423 | TTTAAGGATGGTGAT[A/G]AAATGAGTGGGCTGT | 377630 |
| rs190874299 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138899 | ACCCCCACCAACCGC[A/G]AACACCCCACCCACC | 377630 |
| rs191939669 | snp | C/G | | | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136789 | ACGAATGAAACACAC[C/G]CCAAGAGAAAATAGG | 377630 |
| rs192690207 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139705 | ATTGTATAGTGAGTG[C/G]TTTCGGACGTGCGGC | 377630 |
| rs199527069 | snp | A/C | 0.00498752 | 0.0496879 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138782 | CGCAACAAGGATCAC[A/C]AGGTTTTTCTGCTGG | 377630 |
| rs199641899 | snp | G/T | 0.00199795 | 0.0315433 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138768 | TCCTCCATGTCGCCC[G/T]CAACAAGGATCACAA | 377630 |
| rs199650341 | snp | A/G | 0.00064298 | 0.0179186 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138470 | CGGTGTGTATGTCAG[A/G]CACTGCAGGGAAGCG | 377630 |
| rs199686618 | snp | C/T | 0.0029955 | 0.0385847 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137959 | CAGAAGTGTGTAAAG[C/T]TAACGTCTTGGAGGC | 377630 |
| rs199698022 | snp | A/C/T | 3.2448e-05 | 0.00402777 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137795 | CCCAGCGTGGACCAG[A/C/T]ACAGCATAGAGGACA | 377630 |
| rs199737005 | snp | A/G | 0.228248 | 0.249052 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138761 | TGAGTCGTCCTCCAT[A/G]TCGCCCGCAACAAGG | 377630 |
| rs199744133 | snp | A/G | 0.000884271 | 0.0210084 | stop-gained, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137557 | CTCCTTGCGTTGCTC[A/G]CCTGTCTGTGTCTTC | 377630 |
| rs199820662 | in-del | -/TTT | | | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137110 | GCGCTTGTGGGTGTA[-/TTT]GTGCGTGTGTGTGTG | 377630 |
| rs199873562 | snp | C/G/T | 0.000399281 | 0.0141238 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138217 | AGTGATGATCTACCT[C/G/T]CTTGTGGCCGGGAAG | 377630 |
| rs199889083 | snp | C/T | 0.00226517 | 0.0335776 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137263 | GGGTGCCAGTGTTCA[C/T]GGACTCCTGATCTGT | 377630 |
| rs199901410 | snp | C/T | 0.000477239 | 0.0154399 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137734 | TATACCACTGGCCTT[C/T]TTGAGCTTTGACATA | 377630 |
| rs199901434 | snp | C/G | 0.40601 | 0.195348 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138627 | TCGACACGGGCCTCA[C/G]ATGAGAGTGGTGACT | 377630 |
| rs199933410 | snp | A/C | 0.00199805 | 0.0315441 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138206 | GGTGTCCTTAGAGTG[A/C]TGATCTACCTGCTTG | 377630 |
| rs199935289 | snp | A/C | 0.00553686 | 0.0523237 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137207 | CTTGCTGTGTTTGTT[A/C]TTCCCTTTGGATCTC | 377630 |
| rs199961106 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139078 | TAGGCACATATAATA[G/T]GAGTGTAACCGGGTT | 377630 |
| rs199975575 | snp | G/T | | | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137076 | GTTCGTGTTTGTGTG[G/T]GTGTGTGTGTTTGCG | 377630 |
| rs199985479 | snp | C/G/T | 0.000580046 | 0.0170204 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138613 | AATCATCACAGAGGT[C/G/T]GACACGGGCCTCAGA | 377630 |
| rs200007558 | snp | A/G | 3.84275e-05 | 0.00438318 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137657 | GATGTAAAAGAGGAC[A/G]TAGGCCTGTTGACTC | 377630 |
| rs200055041 | snp | C/T | 0.00485323 | 0.049021 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138384 | TGAGCTTGCATAGTA[C/T]AGAGCATGCAGCACT | 377630 |
| rs200097527 | snp | C/T | 0.00199808 | 0.0315443 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138290 | ATGGGCATCTTCCTG[C/T]TTGCCTCTATGGAAG | 377630 |
| rs200166010 | snp | A/C | 0.001998 | 0.0315438 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137266 | TGCCAGTGTTCACGG[A/C]CTCCTGATCTGTCCG | 377630 |
| rs200186296 | snp | C/G | 0.00745554 | 0.0605985 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138512 | GGTATTTCCCATATT[C/G]TGGAGCCCAGCCCCC | 377630 |
| rs200249593 | snp | A/T | 7.54309e-05 | 0.00614083 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138317 | GAAGCCAGCAGCCAA[A/T]GCCTGTGAGGGCTGG | 377630 |
| rs200378249 | snp | C/T | 0.00305962 | 0.0389929 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137395 | GAGGCAGGGTACCTT[C/T]GACTTTTCTGACGTT | 377630 |
| rs200391244 | snp | A/T | 0.00299542 | 0.0385841 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137301 | GTCGAAGAGAGGTTT[A/T]GCAGGGAGCTTTGCT | 377630 |
| rs200401854 | snp | C/G | 0.00392926 | 0.0441496 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138224 | ATCTACCTGCTTGTG[C/G]CCGGGAAGGCATGCC | 377630 |
| rs200443434 | snp | A/C | 0.159688 | 0.233117 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138765 | TCGTCCTCCATGTCG[A/C]CCGCAACAAGGATCA | 377630 |
| rs200492364 | snp | A/G | 0.000399281 | 0.0141238 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138691 | AAGCTGCATCTGGCC[A/G]AGAAGATGTGAGTTT | 377630 |
| rs200542375 | snp | G/T | 7.82748e-05 | 0.0062555 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138789 | AGGATCACAAGGTTT[G/T]TCTGCTGGGACTGCA | 377630 |
| rs200554002 | snp | A/C/G | 0.0749514 | 0.178491 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137739 | CACTGGCCTTCTTGA[A/C/G]CTTTGACATAAGAGA | 377630 |
| rs200589902 | snp | A/G/T | 0.000294536 | 0.0121322 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137494 | CTCTTTCCACCAAGC[A/G/T]CTCGTCCAACTCGGG | 377630 |
| rs200596158 | snp | A/G | 3.86713e-05 | 0.00439706 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138515 | ATTTCCCATATTCTG[A/G]AGCCCAGCCCCCACC | 377630 |
| rs200644340 | snp | A/G | 0.00302715 | 0.0387868 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137523 | GGTGCCTGGAGGCAG[A/G]GGTGGTCTCTCTTGA | 377630 |
| rs200666853 | snp | G/T | 0.000112011 | 0.00748284 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137890 | GCACATTCTTGGCAA[G/T]TTTGTTGCCTGTGAC | 377630 |
| rs200695704 | snp | A/G | 0.00029576 | 0.012157 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137442 | TTGTTTTGCTCTTGG[A/G]GGAATTTCCAGTGGT | 377630 |
| rs200698817 | snp | C/T | 0.137048 | 0.223029 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138212 | CTTAGAGTGATGATC[C/T]ACCTGCTTGTGGCCG | 377630 |
| rs200736525 | snp | C/G | 9.80873e-05 | 0.00700243 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138769 | CCTCCATGTCGCCCG[C/G]AACAAGGATCACAAG | 377630 |
| rs200743885 | snp | A/G | 0.00199809 | 0.0315444 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137816 | ATAGAGGACATAGAC[A/G]AGAGGTCCTGTGTTC | 377630 |
| rs200843941 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139204 | TGTGTGTGTGTGTGT[G/T]TTTGTGTGTGTGTGT | 377630 |
| rs200898196 | snp | C/G | 0.00598194 | 0.0543616 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137275 | TCACGGACTCCTGAT[C/G]TGTCCGGGTCGTCGA | 377630 |
| rs200899505 | snp | A/T | 0.00697541 | 0.0586434 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138734 | GAACTGCCACTCACC[A/T]CCCAAGTAGAGTGAG | 377630 |
| rs200922971 | snp | C/G | | | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136803 | CCCCAAGAGAAAATA[C/G]GAAACCGAGTCCCCT | 377630 |
| rs200947217 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139404 | CCGTGGCATCAAACA[A/G]ACCTTCCAGGGATAA | 377630 |
| rs200968917 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139854 | ATACTATTTCCATAC[G/T]TACGTGATAATGGAT | 377630 |
| rs201012791 | snp | A/G | 0.00141966 | 0.0266047 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137286 | TGATCTGTCCGGGTC[A/G]TCGAAGAGAGGTTTA | 377630 |
| rs201021467 | snp | C/T | 0.0168555 | 0.0902422 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137154 | CTACGTGTGGGTCGG[C/T]ACTTCCACTGAGATC | 377630 |
| rs201032518 | snp | C/T | 0.000155051 | 0.00880348 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138525 | TTCTGGAGCCCAGCC[C/T]CCACCGCAGCAGGTC | 377630 |
| rs201043868 | snp | A/T | 0.24152 | 0.249856 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137573 | CCTGTCTGTGTCTTC[A/T]GCGCCGAGGGCTCTT | 377630 |
| rs201082219 | snp | A/C/G | 9.35697e-05 | 0.00683938 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138614 | ATCATCACAGAGGTC[A/C/G]ACACGGGCCTCAGAT | 377630 |
| rs201211038 | snp | C/T | 0.00924489 | 0.0673571 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138429 | GTTTGAGAGTGCTCC[C/T]GGGACAGCATGTAGT | 377630 |
| rs201221900 | snp | C/T | 0.015872 | 0.0876589 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137227 | CTTTGGATCTCCTGG[C/T]CCTCCCTTGCAGAGA | 377630 |
| rs201233406 | snp | A/T | 0.00407382 | 0.0449479 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137874 | AGGCACTCAGGATAT[A/T]GCACATTCTTGGCAA | 377630 |
| rs201263364 | snp | A/G | 1.78573e-05 | 0.00298803 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137696 | AGTGATGCTACAGGC[A/G]GTGACCTTGGCATCA | 377630 |
| rs201273969 | snp | C/T | 0.491243 | 0.065589 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138031 | CTCCATTGAGTTCTT[C/T]GGGCTTCACCAACTG | 377630 |
| rs201297814 | snp | A/G/T | 0.00121753 | 0.0246438 | stop-gained, missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137355 | CCACACTTGTATTTC[A/G/T]ATTGATGAATCACAA | 377630 |
| rs201301216 | snp | C/T | 4.65387e-05 | 0.00482361 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138767 | GTCCTCCATGTCGCC[C/T]GCAACAAGGATCACA | 377630 |
| rs201338909 | snp | C/G | 0.000117162 | 0.00765294 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138467 | GGGCGGTGTGTATGT[C/G]AGGCACTGCAGGGAA | 377630 |
| rs201342238 | snp | A/C | 0.00236524 | 0.0343078 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137772 | TAATGTCCGTCGTGA[A/C]AACTCCACCCAGCGT | 377630 |
| rs201369910 | snp | A/C | 0.00197529 | 0.0313647 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138295 | CATCTTCCTGCTTGC[A/C]TCTATGGAAGCCAGC | 377630 |
| rs201388817 | snp | C/G/T | 1.84371e-05 | 0.00303615 | synonymous-codon, missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137471 | GTCTAAGGTGCTTTC[C/G/T]TGAGTGGCTCTTTCC | 377630 |
| rs201482164 | in-del | -/GG | | | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137074 | TGTTCGTGTTTGTGT[-/GG]GTGTGTGTGTGTTTG | 377630 |
| rs201511923 | snp | G/T | | | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138459 | TTGGCAAGGGGCGGT[G/T]TGTATGTCAGGCACT | 377630 |
| rs201523325 | snp | A/G | 5.20594e-05 | 0.00510166 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137694 | GAAGTGATGCTACAG[A/G]CAGTGACCTTGGCAT | 377630 |
| rs201531131 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139228 | TGTGTGTGTGTGCTT[G/T]TGCTGGGATGAACTT | 377630 |
| rs201543463 | snp | C/T | 0.00299556 | 0.0385851 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137318 | CAGGGAGCTTTGCTG[C/T]TCAGGATGATGGTTT | 377630 |
| rs201618621 | snp | A/G | 0.00103457 | 0.0227203 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137424 | TTGAACTCAGGCTTC[A/G]TTTTGTTTTGCTCTT | 377630 |
| rs201643410 | snp | G/T | 7.47231e-05 | 0.00611195 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138580 | TCCTGGGAGCAAGCT[G/T]TCTTGCCACAGGAGC | 377630 |
| rs201644713 | snp | A/G | 0.00199802 | 0.0315439 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138200 | GAGGGTGGTGTCCTT[A/G]GAGTGATGATCTACC | 377630 |
| rs201647724 | snp | C/T | 0.18451 | 0.24127 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138314 | ATGGAAGCCAGCAGC[C/T]AATGCCTGTGAGGGC | 377630 |
| rs201676787 | snp | C/G | 1.78979e-05 | 0.00299143 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137691 | ACAGAAGTGATGCTA[C/G]AGGCAGTGACCTTGG | 377630 |
| rs201711234 | snp | C/G | | | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137041 | TTGGACTCCTCATTA[C/G]TTTATGTAGGATTGA | 377630 |
| rs201725196 | snp | A/G | 0.00199794 | 0.0315432 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138694 | CTGCATCTGGCCGAG[A/G]AGATGTGAGTTTTGA | 377630 |
| rs201734663 | snp | A/G/T | 0.00166153 | 0.0287821 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138517 | TTCCCATATTCTGGA[A/G/T]CCCAGCCCCCACCGC | 377630 |
| rs201786992 | snp | G/T | 0.000462414 | 0.0151985 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138686 | AGCAAAAGCTGCATC[G/T]GGCCGAGAAGATGTG | 377630 |
| rs201838449 | snp | A/C/G | 0.00156312 | 0.0279134 | missense, synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137498 | TTCCACCAAGCGCTC[A/C/G]TCCAACTCGGGTGCC | 377630 |
| rs201875761 | snp | C/T | 0.000473784 | 0.015384 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138405 | ATGCAGCACTTGGGA[C/T]GCTGACATGTTTGAG | 377630 |
| rs201878486 | snp | C/T | 1.87989e-05 | 0.0030658 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138622 | AGAGGTCGACACGGG[C/T]CTCAGATGAGAGTGG | 377630 |
| rs201880970 | snp | A/T | 0.00199803 | 0.031544 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137181 | GATCACTGGCACACA[A/T]GCAGAGCCCTCTTGC | 377630 |
| rs201894585 | snp | A/G | 0.0758796 | 0.179394 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138213 | TTAGAGTGATGATCT[A/G]CCTGCTTGTGGCCGG | 377630 |
| rs201947742 | snp | A/G/T | 0.00334761 | 0.0407755 | missense, synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137674 | AGGCCTGTTGACTCA[A/G/T]GACAGAAGTGATGCT | 377630 |
| rs201956678 | snp | A/G | 0.0025064 | 0.0353118 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137579 | TGTGTCTTCAGCGCC[A/G]AGGGCTCTTGGTTCC | 377630 |
| rs201981031 | snp | C/G/T | 0.0258311 | 0.110687 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137878 | ACTCAGGATATTGCA[C/G/T]ATTCTTGGCAAGTTT | 377630 |
| rs201994056 | snp | A/G | 0.00199808 | 0.0315444 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137948 | GAGGACCTTGGCAGA[A/G]GTGTGTAAAGTTAAC | 377630 |
| rs202041639 | snp | A/G | 0.0178379 | 0.0927404 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138773 | CATGTCGCCCGCAAC[A/G]AGGATCACAAGGTTT | 377630 |
| rs202050503 | snp | A/T | 0.219216 | 0.248098 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138276 | AACATGAGAAATTCA[A/T]GGGCATCTTCCTGCT | 377630 |
| rs202055669 | snp | C/T | 0.00289366 | 0.037927 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137391 | TTGGGAGGCAGGGTA[C/T]CTTCGACTTTTCTGA | 377630 |
| rs202074151 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139174 | TGAAACCGTGTGTGT[A/C]TCTCTCTGTGTGTGT | 377630 |
| rs202079411 | snp | A/T | 0.00199806 | 0.0315442 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137287 | GATCTGTCCGGGTCG[A/T]CGAAGAGAGGTTTAG | 377630 |
| rs202133102 | snp | A/T | 0.000184328 | 0.00959845 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137257 | AAGCGAGGGTGCCAG[A/T]GTTCACGGACTCCTG | 377630 |
| rs202147143 | snp | A/G | 0.013902 | 0.0822054 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137240 | GGTCCTCCCTTGCAG[A/G]GAAGCGAGGGTGCCA | 377630 |
| rs202208366 | snp | A/G | 0.000590744 | 0.0171762 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137326 | TTTGCTGTTCAGGAT[A/G]ATGGTTTTTCATCCC | 377630 |
| rs267601744 | snp | C/G/T | 0.000423558 | 0.0145475 | USP17L2, FAM66D | 8 | allele_origin=T(somatic)/C(germline) | 8:12137556 | TCTCCTTGCGTTGCT[C/G/T]GCCTGTCTGTGTCTT | 377630 |
| rs267601745 | snp | C/T | | | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138566 | CAGAGGAAGCTTCTT[C/T]CTGGGAGCAAGCTGT | 377630 |
| rs367856582 | snp | G/T | 0.000346913 | 0.0131657 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138327 | GCCAATGCCTGTGAG[G/T]GCTGGATGACATGAC | 377630 |
| rs367894493 | snp | A/G | 0.000821837 | 0.0202545 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138380 | GATGTGAGCTTGCAT[A/G]GTACAGAGCATGCAG | 377630 |
| rs368031739 | snp | A/G | | | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136757 | AAATTTCACCTTCTC[A/G]TGCCGCCCAACAACT | 377630 |
| rs368095573 | snp | A/T | 0.000149793 | 0.00865298 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138576 | TTCTTCCTGGGAGCA[A/T]GCTGTCTTGCCACAG | 377630 |
| rs368442784 | snp | A/G | | | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136849 | TCAAACCTACACGTC[A/G]GTAGGTCATATTCAG | 377630 |
| rs368449254 | snp | A/G | 0.000421674 | 0.0145141 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138650 | TGGTGACTTCTCAGG[A/G]AGAGAAGTCCGCTGG | 377630 |
| rs368543324 | snp | A/G | 0.000737964 | 0.0191947 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137597 | GGCTCTTGGTTCCCT[A/G]CCTCTTGACACACTC | 377630 |
| rs368815012 | snp | A/G | 2.23471e-05 | 0.00334261 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138440 | CTCCCGGGACAGCAT[A/G]TAGTTGGCAAGGGGC | 377630 |
| rs369125673 | snp | G/T | 0.000144107 | 0.0084872 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137865 | TGCATGTCAAGGCAC[G/T]CAGGATATTGCACAT | 377630 |
| rs369195548 | snp | A/G/T | 3.68591e-05 | 0.00429283 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137478 | GTGCTTTCCTGAGTG[A/G/T]CTCTTTCCACCAAGC | 377630 |
| rs369199590 | snp | A/G/T | 0.000387691 | 0.0139176 | missense, synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138485 | GCACTGCAGGGAAGC[A/G/T]TTCTCGTAGCAGGTA | 377630 |
| rs369233485 | snp | C/T | | | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136984 | GCTCATCCTGAGATG[C/T]AGCCATCACTATCCA | 377630 |
| rs369673487 | snp | A/C/G | 0.000107116 | 0.00731755 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137701 | TGCTACAGGCAGTGA[A/C/G]CTTGGCATCATCCAT | 377630 |
| rs369686769 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140622 | AACATGAGCAATCCA[C/G]ATGCCGTGGCTTCAC | 377630 |
| rs369752781 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139858 | TATTTCCATACTTAC[A/G]TGATAATGGATCAAC | 377630 |
| rs369802022 | snp | A/G | 1.84534e-05 | 0.00303749 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137302 | TCGAAGAGAGGTTTA[A/G]CAGGGAGCTTTGCTG | 377630 |
| rs370134413 | snp | A/C/G | 0.000535917 | 0.0163612 | missense, synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138332 | TGCCTGTGAGGGCTG[A/C/G]ATGACATGACCAGGA | 377630 |
| rs370175394 | snp | A/G | 0.000329129 | 0.012824 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138522 | ATATTCTGGAGCCCA[A/G]CCCCCACCGCAGCAG | 377630 |
| rs370592139 | snp | C/G/T | 0.00016563 | 0.00909887 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137554 | GCTCTCCTTGCGTTG[C/G/T]TCGCCTGTCTGTGTC | 377630 |
| rs370888261 | snp | C/T | | | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137333 | TTCAGGATGATGGTT[C/T]TTCATCCCACACTTG | 377630 |
| rs370973866 | snp | A/C/G | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140114 | CATCGGTTGTTCATG[A/C/G]TCTGAGATGTTCCCT | 377630 |
| rs371007408 | snp | C/T | 0.000815556 | 0.020177 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137963 | AGTGTGTAAAGTTAA[C/T]GTCTTGGAGGCCGGC | 377630 |
| rs371137381 | snp | A/C/G | 3.87014e-05 | 0.0043988 | missense, synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138494 | GGAAGCGTTCTCGTA[A/C/G]CAGGTATTTCCCATA | 377630 |
| rs371173506 | snp | C/T | 0.00217608 | 0.0329136 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138292 | GGGCATCTTCCTGCT[C/T]GCCTCTATGGAAGCC | 377630 |
| rs371227729 | snp | A/G/T | 0.00048011 | 0.015487 | missense, synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137408 | TTCGACTTTTCTGAC[A/G/T]TTGAACTCAGGCTTC | 377630 |
| rs371265427 | snp | G/T | 0.000424061 | 0.0145551 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137449 | GCTCTTGGGGGAATT[G/T]CCAGTGGTCTAAGGT | 377630 |
| rs371333226 | snp | A/T | | | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136824 | CGAGTCCCCTGCAAT[A/T]ACCTCACACTCAAAC | 377630 |
| rs371735438 | snp | A/C/G/T | 0.00012906 | 0.00803225 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137245 | TCCCTTGCAGAGAAG[A/C/G/T]GAGGGTGCCAGTGTT | 377630 |
| rs371801443 | snp | A/T | 1.93564e-05 | 0.00311092 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138493 | GGGAAGCGTTCTCGT[A/T]GCAGGTATTTCCCAT | 377630 |
| rs371850474 | snp | C/T | 0.00917741 | 0.0671154 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137613 | CCTCTTGACACACTC[C/T]CACTGTGTCTTTCCC | 377630 |
| rs371982744 | snp | A/C/G | 0.000793753 | 0.0199062 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137149 | CACCCCTACGTGTGG[A/C/G]TCGGCACTTCCACTG | 377630 |
| rs372481779 | snp | A/G/T | 0.000183662 | 0.00958143 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137550 | TTGAGCTCTCCTTGC[A/G/T]TTGCTCGCCTGTCTG | 377630 |
| rs372504468 | snp | A/G | 0.021333 | 0.101051 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139502 | GTCTTTGCATGAAAT[A/G]CTCTTGTGGAAGCTA | 377630 |
| rs372605534 | snp | C/T | 0.00893576 | 0.0662422 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137767 | AGAAGTAATGTCCGT[C/T]GTGACAACTCCACCC | 377630 |
| rs373050018 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139019 | CAGACACAGCCCACA[G/T]CATGACTTCTAGAAC | 377630 |
| rs373057283 | snp | A/G | 0.00175905 | 0.0296046 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138454 | TGTAGTTGGCAAGGG[A/G]CGGTGTGTATGTCAG | 377630 |
| rs373156591 | snp | C/T | 0.00396337 | 0.0443394 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137354 | CCCACACTTGTATTT[C/T]GATTGATGAATCACA | 377630 |
| rs373357797 | snp | C/T | 3.69126e-05 | 0.00429592 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137361 | TTGTATTTCGATTGA[C/T]GAATCACAAGTACGT | 377630 |
| rs373473112 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137030 | GAGACAGAAACTTGG[A/G]CTCCTCATTACTTTA | 377630 |
| rs373539693 | snp | C/T | 0.00746977 | 0.0606555 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138513 | GTATTTCCCATATTC[C/T]GGAGCCCAGCCCCCA | 377630 |
| rs373560534 | snp | A/C/T | 3.67926e-05 | 0.00428896 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137505 | AAGCGCTCGTCCAAC[A/C/T]CGGGTGCCTGGAGGC | 377630 |
| rs373607167 | snp | A/G | 0.0010674 | 0.0230773 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137647 | CACTCTTCTGGATGT[A/G]AAAGAGGACATAGGC | 377630 |
| rs373611717 | snp | C/T | 0.000116288 | 0.00762434 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138490 | GCAGGGAAGCGTTCT[C/T]GTAGCAGGTATTTCC | 377630 |
| rs373630969 | snp | A/G | 0.000463822 | 0.0152216 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138531 | AGCCCAGCCCCCACC[A/G]CAGCAGGTCTCCTGC | 377630 |
| rs373850176 | snp | A/C/G | 0.00102334 | 0.022599 | missense, synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137768 | GAAGTAATGTCCGTC[A/C/G]TGACAACTCCACCCA | 377630 |
| rs373957129 | snp | A/C | | | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136763 | CACCTTCTCGTGCCG[A/C]CCAACAACTGACGAA | 377630 |
| rs374024609 | snp | C/T | 4.41511e-05 | 0.00469825 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138339 | GAGGGCTGGATGACA[C/T]GACCAGGACTGTGGA | 377630 |
| rs374048343 | snp | A/G/T | 0.000257831 | 0.0113515 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137964 | GTGTGTAAAGTTAAC[A/G/T]TCTTGGAGGCCGGCG | 377630 |
| rs374111122 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140669 | TCTTATCTCTTTAAG[C/T]GGGACCTAGGAATTG | 377630 |
| rs374193185 | snp | C/G | 0.00398564 | 0.0444627 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136676 | CACCGTTCCTATCTT[C/G]TAAATGCATTCCAGT | 377630 |
| rs374633472 | snp | A/T | 0.000139901 | 0.00836246 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138647 | GAGTGGTGACTTCTC[A/T]GGGAGAGAAGTCCGC | 377630 |
| rs374717555 | snp | A/C/G | 0.000728507 | 0.0190723 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138585 | GGAGCAAGCTGTCTT[A/C/G]CCACAGGAGCCAAAT | 377630 |
| rs374777107 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140386 | ACAGCCCTGGCTTCA[G/T]GGCCCATGAAATTAG | 377630 |
| rs374938860 | snp | A/T | 0.104504 | 0.2033 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139646 | AGACTAATTGATGAC[A/T]TTCCCCAAATTTATG | 377630 |
| rs374973302 | snp | A/G/T | 0.000406098 | 0.0142441 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137396 | AGGCAGGGTACCTTC[A/G/T]ACTTTTCTGACGTTG | 377630 |
| rs375059946 | snp | C/T | 0.000185632 | 0.00963232 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137785 | GACAACTCCACCCAG[C/T]GTGGACCAGCACAGC | 377630 |
| rs375221330 | snp | C/T | 9.20293e-05 | 0.00678279 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137497 | TTTCCACCAAGCGCT[C/T]GTCCAACTCGGGTGC | 377630 |
| rs375258900 | snp | C/G/T | 0.000166041 | 0.00911033 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137288 | ATCTGTCCGGGTCGT[C/G/T]GAAGAGAGGTTTAGC | 377630 |
| rs375446007 | snp | A/G | 0.000173985 | 0.00932536 | stop-gained, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137737 | ACCACTGGCCTTCTT[A/G]AGCTTTGACATAAGA | 377630 |
| rs375485205 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140139 | TTCCCTCCATTTCCA[G/T]TTATGCATTGTATGG | 377630 |
| rs375554523 | snp | A/G | 0.00125563 | 0.0250248 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137417 | TCTGACGTTGAACTC[A/G]GGCTTCGTTTTGTTT | 377630 |
| rs375634582 | snp | C/T | 0.000322468 | 0.0126937 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138393 | ATAGTACAGAGCATG[C/T]AGCACTTGGGACGCT | 377630 |
| rs376085259 | snp | C/T | 0.000237972 | 0.0109055 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137435 | CTTCGTTTTGTTTTG[C/T]TCTTGGGGGAATTTC | 377630 |
| rs376142222 | snp | G/T | 0.000710411 | 0.0188335 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137589 | GCGCCGAGGGCTCTT[G/T]GTTCCCTGCCTCTTG | 377630 |
| rs376170326 | snp | A/T | 0.000276465 | 0.011754 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137474 | TAAGGTGCTTTCCTG[A/T]GTGGCTCTTTCCACC | 377630 |
| rs376305799 | snp | A/G/T | 0.000221505 | 0.0105219 | missense, synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137375 | ATGAATCACAAGTAC[A/G/T]TTGGGAGGCAGGGTA | 377630 |
| rs376345938 | snp | C/T | 0.000258498 | 0.0113658 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137404 | TACCTTCGACTTTTC[C/T]GACGTTGAACTCAGG | 377630 |
| rs376462624 | snp | A/C | 0.000406309 | 0.0142474 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137339 | ATGATGGTTTTTCAT[A/C]CCACACTTGTATTTC | 377630 |
| rs376475465 | snp | C/G/T | 9.22518e-05 | 0.00679098 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137280 | GACTCCTGATCTGTC[C/G/T]GGGTCGTCGAAGAGA | 377630 |
| rs376658111 | snp | A/G | 0.000972616 | 0.0220309 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138713 | TGTGAGTTTTGAAAA[A/G]TGGTTGAACTGCCAC | 377630 |
| rs376720096 | snp | A/G/T | 0.0135158 | 0.0810894 | synonymous-codon, missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138430 | TTTGAGAGTGCTCCC[A/G/T]GGACAGCATGTAGTT | 377630 |
| rs376725409 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140602 | TCAGAAGAATGTTCC[C/G]CAGAAACATGAGCAA | 377630 |
| rs376732039 | snp | C/T | 0.000553843 | 0.0166317 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137151 | CCCCTACGTGTGGGT[C/T]GGCACTTCCACTGAG | 377630 |
| rs376813561 | snp | A/C/G | 0.000387339 | 0.0139118 | stop-gained, synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138491 | CAGGGAAGCGTTCTC[A/C/G]TAGCAGGTATTTCCC | 377630 |
| rs376813934 | snp | G/T | | | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136834 | GCAATAACCTCACAC[G/T]CAAACCTACACGTCA | 377630 |
| rs376934381 | snp | A/G | 0.00597247 | 0.0543191 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140580 | AGGGAGAAAGGAGCC[A/G]CCATTTTCAGAAGAA | 377630 |
| rs377211618 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139029 | CCACATCATGACTTC[C/T]AGAACACCTGAATCA | 377630 |
| rs377465232 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139351 | GAAGTATAGTATTTA[G/T]CACAGCGTATTTTCT | 377630 |
| rs377536053 | snp | C/T | 0.00033877 | 0.0130104 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137978 | CGTCTTGGAGGCCGG[C/T]GCCCTCTGGAGACAA | 377630 |
| rs377680300 | snp | A/C/G/T | 0.000509858 | 0.01596 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137575 | TGTCTGTGTCTTCAG[A/C/G/T]GCCGAGGGCTCTTGG | 377630 |
| rs397933690 | in-del | -/CTGT | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139181 | TGTGTGTATCTCTCT[-/CTGT]GTGTGTGTGTGTGTG | 377630 |
| rs527934167 | snp | C/T | | | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136845 | ACACTCAAACCTACA[C/T]GTCAGTAGGTCATAT | 377630 |
| rs527934496 | snp | A/C/T | 0.000338742 | 0.0130101 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138690 | AAAGCTGCATCTGGC[A/C/T]GAGAAGATGTGAGTT | 377630 |
| rs528109616 | snp | A/G | 0.052232 | 0.152931 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138121 | GGTCAAAAGTGTCTG[A/G]AATCCCGTGGCAGTG | 377630 |
| rs528142888 | snp | A/G | 3.26014e-05 | 0.00403728 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137859 | TATGGCTGCATGTCA[A/G]GGCACTCAGGATATT | 377630 |
| rs528148243 | snp | C/G/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140619 | AGAAACATGAGCAAT[C/G/T]CAGATGCCGTGGCTT | 377630 |
| rs528153004 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139358 | AGTATTTAGCACAGC[A/G]TATTTTCTTCCTTAA | 377630 |
| rs528236842 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140397 | TTCATGGCCCATGAA[A/G]TTAGGATGATTTTAA | 377630 |
| rs529031322 | snp | C/G | 0.00159617 | 0.0282053 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138225 | TCTACCTGCTTGTGG[C/G]CGGGAAGGCATGCCT | 377630 |
| rs529115078 | snp | A/C | 0.0193772 | 0.0965046 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140509 | AGAAGGCTTCCTATG[A/C]CCGATGTAAAGTGTC | 377630 |
| rs529662981 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139959 | GCCCGGGTGACGGGA[G/T]TGAGGCCCTGTCTGA | 377630 |
| rs530340100 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137065 | GGATTGACGGTGTTC[A/G]TGTTTGTGTGTGTGT | 377630 |
| rs530446647 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140390 | CCCTGGCTTCATGGC[C/G/T]CATGAAATTAGGATG | 377630 |
| rs530579504 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140102 | CCTGGATTCTCGCAT[C/T]GGTTGTTCATGCTCT | 377630 |
| rs531558806 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139666 | CCAAATTTATGTGTG[C/T]CAGAAAAGAGAGATG | 377630 |
| rs531630119 | snp | C/G | 3.37718e-05 | 0.00410911 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138715 | TGAGTTTTGAAAAGT[C/G]GTTGAACTGCCACTC | 377630 |
| rs532066047 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138891 | TATAACTCACCCCCA[A/C]CAACCGCGAACACCC | 377630 |
| rs532113322 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136730 | ATGATCCATGGATGT[A/G]CCACATGAGCAAAAT | 377630 |
| rs532313822 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139697 | GTCCTGACATTGTAT[A/G]GTGAGTGGTTTCGGA | 377630 |
| rs532555225 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139319 | GAAGTGCGCTTTCTG[A/G]CCTGAGAATAGTCAA | 377630 |
| rs532867677 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136940 | TCGGAAGACTCACGA[A/C]CCCAAAACTTGATGT | 377630 |
| rs533064338 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140044 | ACCTTTTTAATACTG[C/G]CTCTTGTTTCACTGG | 377630 |
| rs533074191 | snp | C/T | 0.000555247 | 0.0166528 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138644 | TGAGAGTGGTGACTT[C/T]TCAGGGAGAGAAGTC | 377630 |
| rs533374101 | snp | A/G | 9.69829e-05 | 0.0069629 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138480 | GTCAGGCACTGCAGG[A/G]AAGCGTTCTCGTAGC | 377630 |
| rs533483810 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140717 | TAACTGCTTTTGAGG[G/T]GAGCCGAATTGATGT | 377630 |
| rs533627925 | snp | A/G | 0.00123686 | 0.0248375 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138260 | CATGGCATCCACAGT[A/G]AACATGAGAAATTCA | 377630 |
| rs533952142 | snp | A/G | 0.00112301 | 0.0236695 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138293 | GGCATCTTCCTGCTT[A/G]CCTCTATGGAAGCCA | 377630 |
| rs533986354 | snp | A/G | 0.000316699 | 0.0125797 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137979 | GTCTTGGAGGCCGGC[A/G]CCCTCTGGAGACAAA | 377630 |
| rs533996834 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138959 | TCAGCACTCAATTAA[A/G]GAATGAGTCACAGGG | 377630 |
| rs534039703 | snp | A/T | 0.000321165 | 0.012668 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138771 | TCCATGTCGCCCGCA[A/T]CAAGGATCACAAGGT | 377630 |
| rs534480114 | in-del | -/G | 0.00835141 | 0.0640778 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139291 | CTCTCATCGACGGAA[-/G]GACAAGAAGTCTGAA | 377630 |
| rs535048287 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138835 | CTATCTCTTCCAAGA[C/G]AGTCTTCAAATGACG | 377630 |
| rs535200959 | snp | A/C | 0.00012864 | 0.00801894 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137520 | TCGGGTGCCTGGAGG[A/C]AGGGGTGGTCTCTCT | 377630 |
| rs535303206 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139980 | CCCTGTCTGAAGAAG[A/G]AAACATCGGAGACGT | 377630 |
| rs535865946 | snp | C/T | 0.000572204 | 0.0169049 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137315 | TAGCAGGGAGCTTTG[C/T]TGTTCAGGATGATGG | 377630 |
| rs535903706 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137105 | CGTGCGCGCTTGTGG[A/G]TGTATTTGTGCGTGT | 377630 |
| rs535989630 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139452 | TATTGACTCTCTATC[C/T]GAGTGAAATTACTGG | 377630 |
| rs536078447 | snp | C/G | 0.000106734 | 0.00730449 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137935 | TCAAGACAAGGATGA[C/G]GACCTTGGCAGAAGT | 377630 |
| rs536115308 | snp | C/G/T | 1.8618e-05 | 0.00305101 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137665 | AGAGGACATAGGCCT[C/G/T]TTGACTCAGGACAGA | 377630 |
| rs536775478 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136681 | TTCCTATCTTCTAAA[C/T]GCATTCCAGTTTCCA | 377630 |
| rs536784051 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139966 | TGACGGGAGTGAGGC[C/G]CTGTCTGAAGAAGAA | 377630 |
| rs537188972 | snp | A/G | 0.000110834 | 0.00744344 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137329 | GCTGTTCAGGATGAT[A/G]GTTTTTCATCCCACA | 377630 |
| rs537418823 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138814 | ACTGCAGGTTGCAGC[A/G]AGACGCTATCTCTTC | 377630 |
| rs537626739 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139743 | TAAGAAAACTTGAAA[A/C]AAAAAACTTGAGAAA | 377630 |
| rs537911522 | snp | A/C/T | 7.56051e-05 | 0.006148 | synonymous-codon, missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138560 | GCTACTCAGAGGAAG[A/C/T]TTCTTCCTGGGAGCA | 377630 |
| rs537998574 | snp | A/C | 0.000149078 | 0.00863231 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138308 | GCCTCTATGGAAGCC[A/C]GCAGCCAATGCCTGT | 377630 |
| rs538178201 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139066 | TCCTCAGGGTGATAG[A/G]CACATATAATATGAG | 377630 |
| rs538226400 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139421 | CCTTCCAGGGATAAC[C/G]TTTCCACGTTCAGCC | 377630 |
| rs538323246 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139132 | TTATTTTAGGTAAAA[A/G]AATGTCAGGGAAGAA | 377630 |
| rs538965023 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137091 | TGTGTGTGTGTTTGC[A/G]TGCGCGCTTGTGGGT | 377630 |
| rs539785886 | snp | G/T | 0.000457452 | 0.0151168 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137968 | GTAAAGTTAACGTCT[G/T]GGAGGCCGGCGCCCT | 377630 |
| rs539797970 | snp | C/T | 3.57028e-05 | 0.00422494 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137702 | GCTACAGGCAGTGAC[C/T]TTGGCATCATCCATT | 377630 |
| rs539886201 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140263 | CTTCAGGCTCTCTGG[C/T]TTACCAGGAATGAAG | 377630 |
| rs540051886 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139856 | ACTATTTCCATACTT[A/G]CGTGATAATGGATCA | 377630 |
| rs540342116 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140641 | CCGTGGCTTCACACA[A/G]GGTGTTGGATGGTCT | 377630 |
| rs540578683 | snp | A/C | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138587 | AGCAAGCTGTCTTGC[A/C]ACAGGAGCCAAATCA | 377630 |
| rs541506280 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139324 | GCGCTTTCTGACCTG[A/G]GAATAGTCAATGAAG | 377630 |
| rs541531993 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139987 | TGAAGAAGAAAACAT[C/T]GGAGACGTTTAAAAG | 377630 |
| rs541610960 | snp | C/T | 0.000399281 | 0.0141238 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138030 | TCTCCATTGAGTTCT[C/T]CGGGCTTCACCAACT | 377630 |
| rs541755368 | snp | A/G | 5.53684e-05 | 0.00526129 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137167 | GGCACTTCCACTGAG[A/G]TCACTGGCACACAAG | 377630 |
| rs541932457 | snp | A/G | 0.0322114 | 0.122752 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139820 | GAAAATAAAAACAAC[A/G]TATCTCACAGCATGG | 377630 |
| rs542080553 | snp | A/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140514 | GCTTCCTATGCCCGA[A/T]GTAAAGTGTCCTGGG | 377630 |
| rs542229963 | snp | A/C/G | 0.000166145 | 0.00911315 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137378 | AATCACAAGTACGTT[A/C/G]GGAGGCAGGGTACCT | 377630 |
| rs542592124 | snp | A/G/T | 9.18646e-05 | 0.00677683 | missense, synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137525 | TGCCTGGAGGCAGGG[A/G/T]TGGTCTCTCTTGAGC | 377630 |
| rs542885045 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138873 | TGGCCGCATCAGCCC[A/T]TATATAACTCACCCC | 377630 |
| rs543587219 | snp | C/T | 1.84752e-05 | 0.00303929 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137139 | TGTGTGCGTTCACCC[C/T]TACGTGTGGGTCGGC | 377630 |
| rs543682833 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138934 | AGGTGTGCGATAAAC[C/T]AATCAAATATCAGCA | 377630 |
| rs543723272 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139515 | ATGCTCTTGTGGAAG[C/G]TAGGCTGCCAAATAA | 377630 |
| rs544098364 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139309 | CAAGAAGTCTGAAGT[A/G]CGCTTTCTGACCTGA | 377630 |
| rs545092534 | snp | C/T | 0.00755907 | 0.0610114 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138849 | AGAGTCTTCAAATGA[C/T]GAGCTCTCTGGCCGC | 377630 |
| rs545253975 | snp | A/G | 0.000300562 | 0.0122552 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138649 | GTGGTGACTTCTCAG[A/G]GAGAGAAGTCCGCTG | 377630 |
| rs545498783 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140506 | ATCAGAAGGCTTCCT[A/T]TGCCCGATGTAAAGT | 377630 |
| rs545784343 | snp | G/T | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138062 | TTCCAAAGCTTGCTT[G/T]ACACTCTGAGCTGCC | 377630 |
| rs545805896 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140575 | TCCACAGGGAGAAAG[G/T]AGCCGCCATTTTCAG | 377630 |
| rs545843924 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140392 | CTGGCTTCATGGCCC[A/T]TGAAATTAGGATGAT | 377630 |
| rs546068829 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139270 | CTTTTGGCAGCTACC[A/G]TCATCCTCTCATCGA | 377630 |
| rs546691337 | snp | C/T | 0.0228977 | 0.104521 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138204 | GTGGTGTCCTTAGAG[C/T]GATGATCTACCTGCT | 377630 |
| rs546986858 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139702 | GACATTGTATAGTGA[A/G]TGGTTTCGGACGTGC | 377630 |
| rs547215885 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140421 | ATTTTAAGGATGGTG[A/G]TGAAATGAGTGGGCT | 377630 |
| rs547297444 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139947 | TACCGTAGAAAAGCC[C/T]GGGTGACGGGAGTGA | 377630 |
| rs547457226 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136985 | CTCATCCTGAGATGC[A/G]GCCATCACTATCCAG | 377630 |
| rs547919956 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138926 | CACCCATCAGGTGTG[C/T]GATAAACCAATCAAA | 377630 |
| rs548079218 | snp | A/G | 5.71195e-05 | 0.00534383 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137582 | GTCTTCAGCGCCGAG[A/G]GCTCTTGGTTCCCTG | 377630 |
| rs548079878 | snp | C/G | | | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136915 | ACACACAGACAGTCT[C/G]TCCAGAGGTTCGGAA | 377630 |
| rs548676924 | snp | C/T | 0.000129102 | 0.00803334 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137211 | CTGTGTTTGTTCTTC[C/T]CTTTGGATCTCCTGG | 377630 |
| rs548701711 | snp | C/G | 0.00279162 | 0.0372561 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137019 | TCCCTGTTGTAGAGA[C/G]AGAAACTTGGACTCC | 377630 |
| rs548964492 | snp | C/G | 0.000399281 | 0.0141238 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138520 | CCATATTCTGGAGCC[C/G]AGCCCCCACCGCAGC | 377630 |
| rs549223964 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139013 | ATTCAACAGACACAG[C/T]CCACATCATGACTTC | 377630 |
| rs549702401 | snp | A/G | 0.000147479 | 0.0085859 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137246 | CCCTTGCAGAGAAGC[A/G]AGGGTGCCAGTGTTC | 377630 |
| rs549741694 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139685 | AAAAGAGAGATGGTC[A/C]TGACATTGTATAGTG | 377630 |
| rs549899331 | snp | A/C | 0.0217236 | 0.101931 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138896 | CTCACCCCCACCAAC[A/C]GCGAACACCCCACCC | 377630 |
| rs550068244 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139414 | AAACAGACCTTCCAG[C/G]GATAACCTTTCCACG | 377630 |
| rs550178667 | snp | C/G/T | 0.000343822 | 0.0131078 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138730 | GGTTGAACTGCCACT[C/G/T]ACCTCCCAAGTAGAG | 377630 |
| rs550855695 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139523 | GTGGAAGCTAGGCTG[A/C]CAAATAATAAAGCAT | 377630 |
| rs551142835 | snp | C/T | 0.00159617 | 0.0282053 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138226 | CTACCTGCTTGTGGC[C/T]GGGAAGGCATGCCTT | 377630 |
| rs551181727 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140690 | CTAGGAATTGTTGTC[C/T]TTTAATGCTCATAAC | 377630 |
| rs551224100 | snp | A/G/T | 0.000492242 | 0.0156808 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137952 | ACCTTGGCAGAAGTG[A/G/T]GTAAAGTTAACGTCT | 377630 |
| rs551358684 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140723 | CTTTTGAGGTGAGCC[A/G]AATTGATGTCCTGCC | 377630 |
| rs551597374 | snp | C/T | 0.000656992 | 0.0181125 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138756 | TAGAGTGAGTCGTCC[C/T]CCATGTCGCCCGCAA | 377630 |
| rs552003581 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140116 | TCGGTTGTTCATGCT[C/G]TGAGATGTTCCCTCC | 377630 |
| rs552020657 | snp | C/T | 0.000135687 | 0.00823558 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138487 | ACTGCAGGGAAGCGT[C/T]CTCGTAGCAGGTATT | 377630 |
| rs552732363 | snp | A/T | 0.00874735 | 0.0655527 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139968 | ACGGGAGTGAGGCCC[A/T]GTCTGAAGAAGAAAA | 377630 |
| rs552789468 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140346 | AGAATTGAGGCCCGG[C/T]GCCAAGGCCTCTGGG | 377630 |
| rs553364730 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139812 | GAACTGATGAAAATA[A/C]AAACAACGTATCTCA | 377630 |
| rs553386797 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139436 | CTTTCCACGTTCAGC[C/G]TATTGACTCTCTATC | 377630 |
| rs553474966 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139165 | CTTTACCTATGAAAC[C/T]GTGTGTGTATCTCTC | 377630 |
| rs553486248 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137094 | GTGTGTGTTTGCGTG[C/T]GCGCTTGTGGGTGTA | 377630 |
| rs553551881 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140182 | TAGCACCTTTGATGC[A/G]AAAATTGTAATGCTG | 377630 |
| rs553639667 | snp | A/G | 3.67525e-05 | 0.0042866 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137522 | GGGTGCCTGGAGGCA[A/G]GGGTGGTCTCTCTTG | 377630 |
| rs553727609 | snp | C/T | 1.84613e-05 | 0.00303814 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137366 | TTTCGATTGATGAAT[C/T]ACAAGTACGTTGGGA | 377630 |
| rs554259557 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137116 | GTGGGTGTATTTGTG[C/T]GTGTGTGTGTGTGCG | 377630 |
| rs554653265 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138839 | CTCTTCCAAGAGAGT[C/T]TTCAAATGACGAGCT | 377630 |
| rs555293388 | snp | C/T | 0.00835141 | 0.0640778 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136775 | CCGCCCAACAACTGA[C/T]GAATGAAACACACCC | 377630 |
| rs555355215 | snp | C/T | 9.34658e-05 | 0.00683551 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138603 | ACAGGAGCCAAATCA[C/T]CACAGAGGTCGACAC | 377630 |
| rs555454609 | snp | C/G | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140750 | TGCCTGCGTGTCATG[C/G]TCATTGCACTTTAAT | 377630 |
| rs555548747 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140343 | GGCAGAATTGAGGCC[C/T]GGCGCCAAGGCCTCT | 377630 |
| rs555589842 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136710 | CACTATTCAAGGTGG[C/T]GAGAATGATCCATGG | 377630 |
| rs555784587 | in-del | -/TCTG | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139180 | GTGTGTGTATCTCTC[-/TCTG]TGTGTGTGTGTGTGT | 377630 |
| rs555841201 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139089 | AATATGAGTGTAACC[A/G]GGTTGGGACAGTGGC | 377630 |
| rs556156968 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138818 | CAGGTTGCAGCAAGA[C/T]GCTATCTCTTCCAAG | 377630 |
| rs557074436 | snp | A/G | 5.62177e-05 | 0.00530148 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138311 | TCTATGGAAGCCAGC[A/G]GCCAATGCCTGTGAG | 377630 |
| rs557849574 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140281 | ACCAGGAATGAAGAT[A/C]CTGGCTCTAGGGATT | 377630 |
| rs558684912 | snp | A/C | 0.00199481 | 0.0315187 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136720 | GGTGGCGAGAATGAT[A/C]CATGGATGTGCCACA | 377630 |
| rs558887482 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139955 | AAAAGCCCGGGTGAC[A/G]GGAGTGAGGCCCTGT | 377630 |
| rs558917481 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139764 | ACTTGAGAAATCCAA[A/G]GGTATCCCAACTATA | 377630 |
| rs558972987 | snp | A/C/T | 0.00318978 | 0.0398085 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136843 | TCACACTCAAACCTA[A/C/T]ACGTCAGTAGGTCAT | 377630 |
| rs559049440 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138826 | AGCAAGACGCTATCT[C/T]TTCCAAGAGAGTCTT | 377630 |
| rs559072293 | snp | C/T | 1.85493e-05 | 0.00304537 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137746 | CTTCTTGAGCTTTGA[C/T]ATAAGAGAAGTAATG | 377630 |
| rs559197491 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140073 | GGGAAATGGCAAAAA[A/T]AAACCGTGTATCTCC | 377630 |
| rs559224294 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139517 | GCTCTTGTGGAAGCT[A/C]GGCTGCCAAATAATA | 377630 |
| rs559437840 | snp | G/T | 0.0004426 | 0.0148696 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137195 | AAGCAGAGCCCTCTT[G/T]CTGTGTTTGTTCTTC | 377630 |
| rs559823570 | snp | G/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139581 | TGAAGAGTTACTCAG[G/T]GCACAAAGTAGGCTG | 377630 |
| rs560274818 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138863 | ACGAGCTCTCTGGCC[A/G]CATCAGCCCTTATAT | 377630 |
| rs560363673 | snp | A/C/G/T | 0.00066597 | 0.0182373 | synonymous-codon, missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138661 | CAGGGAGAGAAGTCC[A/C/G/T]CTGGATTTCAGCAAA | 377630 |
| rs561100282 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136912 | CAAACACACAGACAG[G/T]CTCTCCAGAGGTTCG | 377630 |
| rs561225495 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138876 | CCGCATCAGCCCTTA[C/T]ATAACTCACCCCCAC | 377630 |
| rs561491112 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139486 | GTGGAGAACAAGACA[A/G]GTCTTTGCATGAAAT | 377630 |
| rs561872848 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140521 | ATGCCCGATGTAAAG[C/T]GTCCTGGGGGAAGAA | 377630 |
| rs562277148 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140662 | TGGATGGTCTTATCT[C/G]TTTAAGCGGGACCTA | 377630 |
| rs563055870 | snp | C/G | 2.1184e-05 | 0.00325446 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138446 | GGACAGCATGTAGTT[C/G]GCAAGGGGCGGTGTG | 377630 |
| rs563254225 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140377 | TGTAAAGAAACAGCC[C/T]TGGCTTCATGGCCCA | 377630 |
| rs563506903 | snp | A/G | 0.00358779 | 0.0422022 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137014 | AGTTGTCCCTGTTGT[A/G]GAGACAGAAACTTGG | 377630 |
| rs563752100 | snp | A/T | 0.0023933 | 0.0345097 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137213 | GTGTTTGTTCTTCCC[A/T]TTGGATCTCCTGGTC | 377630 |
| rs563974925 | snp | C/G/T | 0.000173501 | 0.00931261 | synonymous-codon, missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137849 | CTGAGACATGTATGG[C/G/T]TGCATGTCAAGGCAC | 377630 |
| rs564039683 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140427 | AGGATGGTGATGAAA[C/T]GAGTGGGCTGTGACC | 377630 |
| rs564069468 | snp | A/G | 0.00206398 | 0.0320582 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138092 | CTGGATATCCAGGGC[A/G]ATGTCCAGGTAAGGG | 377630 |
| rs564364111 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139541 | AATAATAAAGCATCA[A/T]ATGGTAGAAACATGC | 377630 |
| rs564890148 | snp | A/T | 1.84633e-05 | 0.00303831 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137400 | AGGGTACCTTCGACT[A/T]TTCTGACGTTGAACT | 377630 |
| rs564980535 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139873 | GTGATAATGGATCAA[A/C]ATTTCATAGAGATGA | 377630 |
| rs565091946 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139311 | AGAAGTCTGAAGTGC[A/G]CTTTCTGACCTGAGA | 377630 |
| rs565325885 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138897 | TCACCCCCACCAACC[A/G]CGAACACCCCACCCA | 377630 |
| rs565428256 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139444 | GTTCAGCCTATTGAC[A/T]CTCTATCCGAGTGAA | 377630 |
| rs565460675 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136937 | GGTTCGGAAGACTCA[C/T]GACCCCAAAACTTGA | 377630 |
| rs565617098 | snp | C/G/T | 3.68903e-05 | 0.00429465 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137454 | TGGGGGAATTTCCAG[C/G/T]GGTCTAAGGTGCTTT | 377630 |
| rs566038569 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138831 | GACGCTATCTCTTCC[A/G]AGAGAGTCTTCAAAT | 377630 |
| rs566618019 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140491 | GGCCAGGTGTGCTTC[A/G]TCAGAAGGCTTCCTA | 377630 |
| rs567328918 | snp | C/G | 0.000192293 | 0.00980354 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138540 | CCCACCGCAGCAGGT[C/G]TCCTGCTACTCAGAG | 377630 |
| rs567414793 | snp | C/T | 0.000595285 | 0.017242 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138306 | TTGCCTCTATGGAAG[C/T]CAGCAGCCAATGCCT | 377630 |
| rs567431495 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139020 | AGACACAGCCCACAT[C/T]ATGACTTCTAGAACA | 377630 |
| rs567459012 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139387 | AATAATAAAGGAGAT[A/T]TCCGTGGCATCAAAC | 377630 |
| rs568636393 | snp | A/C/G | 0.000148879 | 0.00862666 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137909 | GTTGCCTGTGACATC[A/C/G]GAGAATCTCTTCAAG | 377630 |
| rs568674782 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137663 | AAAGAGGACATAGGC[C/T]TGTTGACTCAGGACA | 377630 |
| rs568764243 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140200 | AATTGTAATGCTGAC[A/G]AAAGTGGACATGTTC | 377630 |
| rs569203829 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140484 | TTTCATGGGCCAGGT[A/G]TGCTTCATCAGAAGG | 377630 |
| rs569395074 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137327 | TTGCTGTTCAGGATG[A/G]TGGTTTTTCATCCCA | 377630 |
| rs569397331 | snp | C/G | 0.00517822 | 0.0506191 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138233 | CTTGTGGCCGGGAAG[C/G]CATGCCTTTTTCATG | 377630 |
| rs570122924 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139719 | GGTTTCGGACGTGCG[G/T]CGGCAGTTTAAGAAA | 377630 |
| rs570513591 | snp | C/G | 2.02051e-05 | 0.00317839 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137636 | TCTTTCCCATTCACT[C/G]TTCTGGATGTAAAAG | 377630 |
| rs571058609 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139973 | AGTGAGGCCCTGTCT[C/G]AAGAAGAAAACATCG | 377630 |
| rs571130591 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139418 | AGACCTTCCAGGGAT[A/G]ACCTTTCCACGTTCA | 377630 |
| rs571503007 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139690 | AGAGATGGTCCTGAC[A/G]TTGTATAGTGAGTGG | 377630 |
| rs571710521 | snp | A/G | 0.00398564 | 0.0444627 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137095 | TGTGTGTTTGCGTGC[A/G]CGCTTGTGGGTGTAT | 377630 |
| rs571835744 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139194 | TCTGTGTGTGTGTGT[G/T]TGTGTGTGTGTTTGT | 377630 |
| rs572038441 | snp | C/T | 0.00199481 | 0.0315187 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136790 | CGAATGAAACACACC[C/T]CAAGAGAAAATAGGA | 377630 |
| rs572323705 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138864 | CGAGCTCTCTGGCCG[A/C]ATCAGCCCTTATATA | 377630 |
| rs572365853 | snp | A/G | | | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136739 | GGATGTGCCACATGA[A/G]CAAAATTTCACCTTC | 377630 |
| rs572909138 | snp | A/C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139964 | GGTGACGGGAGTGAG[A/C/G]CCCTGTCTGAAGAAG | 377630 |
| rs573164975 | snp | C/T | 0.000112085 | 0.0074853 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138586 | GAGCAAGCTGTCTTG[C/T]CACAGGAGCCAAATC | 377630 |
| rs573203952 | snp | C/T | 0.00110441 | 0.0234731 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138342 | GGCTGGATGACATGA[C/T]CAGGACTGTGGAGGG | 377630 |
| rs573278852 | snp | C/T | 1.83775e-05 | 0.00303124 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137735 | ATACCACTGGCCTTC[C/T]TGAGCTTTGACATAA | 377630 |
| rs573688773 | snp | C/G/T | 0.00022497 | 0.0106036 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138618 | TCACAGAGGTCGACA[C/G/T]GGGCCTCAGATGAGA | 377630 |
| rs574299353 | snp | A/G | 1.85517e-05 | 0.00304557 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137747 | TTCTTGAGCTTTGAC[A/G]TAAGAGAAGTAATGT | 377630 |
| rs574772788 | snp | C/T | | | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136801 | CACCCCAAGAGAAAA[C/T]AGGAAACCGAGTCCC | 377630 |
| rs574810542 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138850 | GAGTCTTCAAATGAC[C/G]AGCTCTCTGGCCGCA | 377630 |
| rs575389930 | snp | A/G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140347 | GAATTGAGGCCCGGC[A/G/T]CCAAGGCCTCTGGGT | 377630 |
| rs575494695 | snp | C/G | 0.00566568 | 0.052922 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138046 | CGGGCTTCACCAACT[C/G]TTCCAAAGCTTGCTT | 377630 |
| rs575530104 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140530 | GTAAAGTGTCCTGGG[A/G]GAAGAAAGGAGCACT | 377630 |
| rs575561584 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140262 | TCTTCAGGCTCTCTG[G/T]CTTACCAGGAATGAA | 377630 |
| rs576201574 | snp | A/G/T | 0.000229202 | 0.0107029 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137117 | TGGGTGTATTTGTGC[A/G/T]TGTGTGTGTGTGCGT | 377630 |
| rs576237955 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136914 | AACACACAGACAGTC[C/T]CTCCAGAGGTTCGGA | 377630 |
| rs576659411 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139286 | TCATCCTCTCATCGA[C/T]GGAAGGACAAGAAGT | 377630 |
| rs577493105 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139530 | CTAGGCTGCCAAATA[A/C]TAAAGCATCAAATGG | 377630 |
| rs577539512 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136754 | GCAAAATTTCACCTT[C/G]TCGTGCCGCCCAACA | 377630 |
| rs577601059 | snp | C/G | 0.00874735 | 0.0655527 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139781 | GTATCCCAACTATAA[C/G]CTTTTGTTTATTAAA | 377630 |
| rs577663078 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138822 | TTGCAGCAAGACGCT[A/G]TCTCTTCCAAGAGAG | 377630 |
| rs577891616 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140474 | TCCTTTGTCTTTTCA[G/T]GGGCCAGGTGTGCTT | 377630 |
| rs745333256 | snp | A/T | 0.000168292 | 0.00917157 | stop-gained, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138605 | AGGAGCCAAATCATC[A/T]CAGAGGTCGACACGG | 377630 |
| rs745419434 | snp | C/T | 7.3593e-05 | 0.00606557 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137506 | AGCGCTCGTCCAACT[C/T]GGGTGCCTGGAGGCA | 377630 |
| rs745420166 | snp | C/T | 0.000147366 | 0.00858261 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137982 | TTGGAGGCCGGCGCC[C/T]TCTGGAGACAAAGAC | 377630 |
| rs745525773 | snp | A/G | 2.50598e-05 | 0.00353967 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138802 | TTTTCTGCTGGGACT[A/G]CAGGTTGCAGCAAGA | 377630 |
| rs745694573 | snp | C/G | 1.84705e-05 | 0.0030389 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137145 | CGTTCACCCCTACGT[C/G]TGGGTCGGCACTTCC | 377630 |
| rs745731889 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139844 | AGCATGGGTGATACT[A/G]TTTCCATACTTACGT | 377630 |
| rs745875865 | snp | C/G/T | 5.65056e-05 | 0.00531509 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137866 | GCATGTCAAGGCACT[C/G/T]AGGATATTGCACATT | 377630 |
| rs745974636 | snp | C/T | 0.000129257 | 0.00803816 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137407 | CTTCGACTTTTCTGA[C/T]GTTGAACTCAGGCTT | 377630 |
| rs746104362 | snp | C/T | 6.1078e-05 | 0.00552587 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138689 | AAAAGCTGCATCTGG[C/T]CGAGAAGATGTGAGT | 377630 |
| rs746182586 | snp | C/T | 3.54667e-05 | 0.00421095 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138300 | TCCTGCTTGCCTCTA[C/T]GGAAGCCAGCAGCCA | 377630 |
| rs746272429 | snp | A/G | 3.88214e-05 | 0.00440559 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137654 | CTGGATGTAAAAGAG[A/G]ACATAGGCCTGTTGA | 377630 |
| rs746359926 | snp | C/T | 9.22229e-05 | 0.00678991 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137206 | TCTTGCTGTGTTTGT[C/T]CTTCCCTTTGGATCT | 377630 |
| rs746473450 | snp | C/G | 1.8435e-05 | 0.00303598 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137250 | TGCAGAGAAGCGAGG[C/G]TGCCAGTGTTCACGG | 377630 |
| rs746479899 | snp | C/T | 1.93463e-05 | 0.00311011 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138524 | ATTCTGGAGCCCAGC[C/T]CCCACCGCAGCAGGT | 377630 |
| rs746575891 | snp | A/C/T | 6.38758e-05 | 0.00565106 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137928 | AATCTCTTCAAGACA[A/C/T]GGATGAGGACCTTGG | 377630 |
| rs746721885 | snp | A/G | 1.83984e-05 | 0.00303296 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137503 | CCAAGCGCTCGTCCA[A/G]CTCGGGTGCCTGGAG | 377630 |
| rs746752440 | snp | C/T | 7.48559e-05 | 0.00611738 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138750 | CCCAAGTAGAGTGAG[C/T]CGTCCTCCATGTCGC | 377630 |
| rs746968491 | snp | A/T | 0.000118462 | 0.00769527 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138408 | CAGCACTTGGGACGC[A/T]GACATGTTTGAGAGT | 377630 |
| rs747008099 | snp | A/G | 4.02091e-05 | 0.00448363 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138453 | ATGTAGTTGGCAAGG[A/G]GCGGTGTGTATGTCA | 377630 |
| rs747131547 | snp | A/G | 5.53654e-05 | 0.00526114 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137309 | GAGGTTTAGCAGGGA[A/G]CTTTGCTGTTCAGGA | 377630 |
| rs747217523 | snp | A/G | 1.84619e-05 | 0.00303819 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137370 | GATTGATGAATCACA[A/G]GTACGTTGGGAGGCA | 377630 |
| rs747251824 | snp | A/C | 7.49513e-05 | 0.00612128 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138616 | CATCACAGAGGTCGA[A/C]ACGGGCCTCAGATGA | 377630 |
| rs747513169 | snp | C/T | 0.000125452 | 0.00791899 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138294 | GCATCTTCCTGCTTG[C/T]CTCTATGGAAGCCAG | 377630 |
| rs747590109 | snp | A/G | 1.84653e-05 | 0.00303848 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137152 | CCCTACGTGTGGGTC[A/G]GCACTTCCACTGAGA | 377630 |
| rs747636300 | snp | C/T | 1.98273e-05 | 0.00314853 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137646 | TCACTCTTCTGGATG[C/T]AAAAGAGGACATAGG | 377630 |
| rs747756527 | snp | A/G | 1.93392e-05 | 0.00310954 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138496 | AAGCGTTCTCGTAGC[A/G]GGTATTTCCCATATT | 377630 |
| rs747763652 | snp | C/T | 0.000135406 | 0.00822706 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138518 | TCCCATATTCTGGAG[C/T]CCAGCCCCCACCGCA | 377630 |
| rs747807249 | snp | C/T | | | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137882 | AGGATATTGCACATT[C/T]TTGGCAAGTTTGTTG | 377630 |
| rs747891141 | in-del | -/T | 2.92916e-05 | 0.00382687 | frameshift-variant, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137865 | TGCATGTCAAGGCAC[-/T]CAGGATATTGCACAT | 377630 |
| rs747922407 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139717 | GTGGTTTCGGACGTG[C/T]GGCGGCAGTTTAAGA | 377630 |
| rs748188908 | snp | G/T | 0.000104827 | 0.00723897 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138792 | ATCACAAGGTTTTTC[G/T]GCTGGGACTGCAGGT | 377630 |
| rs748190868 | snp | C/T | 4.5405e-05 | 0.0047645 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138358 | CAGGACTGTGGAGGG[C/T]CCATGTGATGTGAGC | 377630 |
| rs748226288 | snp | G/T | 1.78551e-05 | 0.00298784 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137697 | GTGATGCTACAGGCA[G/T]TGACCTTGGCATCAT | 377630 |
| rs748488772 | snp | C/T | 3.69004e-05 | 0.00429521 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137300 | CGTCGAAGAGAGGTT[C/T]AGCAGGGAGCTTTGC | 377630 |
| rs748610555 | snp | A/C | 0.000513795 | 0.0160198 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137992 | GCGCCCTCTGGAGAC[A/C]AAGACCGCAATGATA | 377630 |
| rs748652021 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138851 | AGTCTTCAAATGACG[A/G]GCTCTCTGGCCGCAT | 377630 |
| rs748697358 | snp | G/T | 1.93033e-05 | 0.00310665 | stop-gained, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138639 | TCAGATGAGAGTGGT[G/T]ACTTCTCAGGGAGAG | 377630 |
| rs748750949 | snp | G/T | 0.000128536 | 0.0080157 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137539 | GGTGGTCTCTCTTGA[G/T]CTCTCCTTGCGTTGC | 377630 |
| rs748812109 | snp | C/T | 0.000154196 | 0.00877919 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138755 | GTAGAGTGAGTCGTC[C/T]TCCATGTCGCCCGCA | 377630 |
| rs748843066 | snp | A/G | 1.84841e-05 | 0.00304002 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137125 | TTTGTGCGTGTGTGT[A/G]TGTGCGTTCACCCCT | 377630 |
| rs748964524 | snp | A/G | 1.95547e-05 | 0.00312682 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138465 | AGGGGCGGTGTGTAT[A/G]TCAGGCACTGCAGGG | 377630 |
| rs749024656 | snp | C/T | 3.68942e-05 | 0.00429485 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137189 | GCACACAAGCAGAGC[C/T]CTCTTGCTGTGTTTG | 377630 |
| rs749111700 | snp | A/G | | | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137477 | GGTGCTTTCCTGAGT[A/G]GCTCTTTCCACCAAG | 377630 |
| rs749208162 | in-del | -/C | 7.88877e-05 | 0.00627994 | frameshift-variant, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137607 | CCCTGCCTCTTGACA[-/C]CACTCTCACTGTGTC | 377630 |
| rs749236918 | snp | A/T | 2.12605e-05 | 0.00326034 | stop-gained, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137920 | CATCGGAGAATCTCT[A/T]CAAGACAAGGATGAG | 377630 |
| rs749247596 | snp | A/G | 3.69447e-05 | 0.00429779 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137413 | CTTTTCTGACGTTGA[A/G]CTCAGGCTTCGTTTT | 377630 |
| rs749324489 | snp | A/T | 3.18446e-05 | 0.00399015 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138695 | TGCATCTGGCCGAGA[A/T]GATGTGAGTTTTGAA | 377630 |
| rs749373882 | snp | C/G/T | 0.000115355 | 0.00759381 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138310 | CTCTATGGAAGCCAG[C/G/T]AGCCAATGCCTGTGA | 377630 |
| rs749429908 | snp | A/G | 7.03482e-05 | 0.00593036 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138739 | GCCACTCACCTCCCA[A/G]GTAGAGTGAGTCGTC | 377630 |
| rs749532784 | snp | G/T | 6.7704e-05 | 0.00581786 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138353 | ATGACCAGGACTGTG[G/T]AGGGCCCATGTGATG | 377630 |
| rs749685000 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140447 | GGGCTGTGACCTTTG[C/G]CCCTGTTTCTTTCCT | 377630 |
| rs749714928 | snp | G/T | 1.8434e-05 | 0.0030359 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137258 | AGCGAGGGTGCCAGT[G/T]TTCACGGACTCCTGA | 377630 |
| rs749798175 | snp | A/C/G | 3.74576e-05 | 0.00432754 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138575 | CTTCTTCCTGGGAGC[A/C/G]AGCTGTCTTGCCACA | 377630 |
| rs749836734 | snp | C/G/T | 5.04579e-05 | 0.00502259 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137840 | TGTGTTCTGCTGAGA[C/G/T]ATGTATGGCTGCATG | 377630 |
| rs749953151 | snp | C/G | 0.000134003 | 0.00818436 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138636 | GCCTCAGATGAGAGT[C/G]GTGACTTCTCAGGGA | 377630 |
| rs750075830 | snp | C/T | 4.77772e-05 | 0.00488736 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138036 | TTGAGTTCTTCGGGC[C/T]TCACCAACTGTTCCA | 377630 |
| rs750087009 | snp | C/G | 8.9811e-05 | 0.00670055 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138673 | TCCGCTGGATTTCAG[C/G]AAAAGCTGCATCTGG | 377630 |
| rs750164077 | snp | A/T | 3.51451e-05 | 0.00419181 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138269 | CACAGTGAACATGAG[A/T]AATTCATGGGCATCT | 377630 |
| rs750253588 | snp | A/C | 2.05746e-05 | 0.00320732 | stop-gained, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137626 | TCTCACTGTGTCTTT[A/C]CCATTCACTCTTCTG | 377630 |
| rs750294287 | snp | A/G | 5.53419e-05 | 0.00526003 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137184 | CACTGGCACACAAGC[A/G]GAGCCCTCTTGCTGT | 377630 |
| rs750416266 | multinucleotide-polymorphism | CGTGTGTGTATCTCTC/TCTATGAAACCGTGTG | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139165 | CTTTACCTATGAAAC[lengthTooLong]TGTGTGTGTGTGTGT | 377630 |
| rs750483315 | snp | A/T | 1.93302e-05 | 0.00310882 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138510 | CAGGTATTTCCCATA[A/T]TCTGGAGCCCAGCCC | 377630 |
| rs750573096 | snp | C/T | 1.92114e-05 | 0.00309924 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138541 | CCACCGCAGCAGGTC[C/T]CCTGCTACTCAGAGG | 377630 |
| rs750600218 | snp | A/G/T | 8.5427e-05 | 0.00653508 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137937 | AAGACAAGGATGAGG[A/G/T]CCTTGGCAGAAGTGT | 377630 |
| rs750855075 | snp | C/G | 2.21875e-05 | 0.00333065 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138343 | GCTGGATGACATGAC[C/G]AGGACTGTGGAGGGC | 377630 |
| rs750950898 | snp | A/G | 2.52784e-05 | 0.00355507 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138390 | TGCATAGTACAGAGC[A/G]TGCAGCACTTGGGAC | 377630 |
| rs751043690 | snp | C/T | 1.81949e-05 | 0.00301614 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137726 | ATCCATTTTATACCA[C/T]TGGCCTTCTTGAGCT | 377630 |
| rs751206247 | snp | C/G | 5.5394e-05 | 0.0052625 | stop-gained, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137348 | TTTCATCCCACACTT[C/G]TATTTCGATTGATGA | 377630 |
| rs751207879 | snp | A/C | 1.86788e-05 | 0.00305599 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138598 | TTGCCACAGGAGCCA[A/C]ATCATCACAGAGGTC | 377630 |
| rs751578611 | snp | A/C | 1.94657e-05 | 0.00311969 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137599 | CTCTTGGTTCCCTGC[A/C]TCTTGACACACTCTC | 377630 |
| rs751608514 | snp | A/C | 1.84739e-05 | 0.00303918 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137141 | TGTGCGTTCACCCCT[A/C]CGTGTGGGTCGGCAC | 377630 |
| rs751709966 | in-del | -/A | 3.20672e-05 | 0.00400407 | frameshift-variant, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138692 | AGCTGCATCTGGCCG[-/A]GAAGATGTGAGTTTT | 377630 |
| rs751716453 | snp | A/G | 0.00015461 | 0.00879097 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138507 | TAGCAGGTATTTCCC[A/G]TATTCTGGAGCCCAG | 377630 |
| rs751716724 | snp | C/G | 1.84541e-05 | 0.00303755 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137173 | TCCACTGAGATCACT[C/G]GCACACAAGCAGAGC | 377630 |
| rs751850291 | snp | C/T | 5.37447e-05 | 0.00518357 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137898 | TTGGCAAGTTTGTTG[C/T]CTGTGACATCGGAGA | 377630 |
| rs752016674 | snp | A/G | 8.87535e-05 | 0.00666099 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138687 | GCAAAAGCTGCATCT[A/G]GCCGAGAAGATGTGA | 377630 |
| rs752026404 | snp | A/C | 1.84225e-05 | 0.00303495 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137486 | CTGAGTGGCTCTTTC[A/C]ACCAAGCGCTCGTCC | 377630 |
| rs752104464 | snp | C/G | 3.42249e-05 | 0.00413658 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138728 | GTGGTTGAACTGCCA[C/G]TCACCTCCCAAGTAG | 377630 |
| rs752178696 | snp | A/T | 1.79599e-05 | 0.00299661 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137686 | TCAGGACAGAAGTGA[A/T]GCTACAGGCAGTGAC | 377630 |
| rs752196507 | snp | G/T | 6.6302e-05 | 0.00575731 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138335 | CTGTGAGGGCTGGAT[G/T]ACATGACCAGGACTG | 377630 |
| rs752369376 | snp | A/T | 1.79861e-05 | 0.00299879 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137718 | TTGGCATCATCCATT[A/T]TATACCACTGGCCTT | 377630 |
| rs752455149 | snp | C/T | 1.84487e-05 | 0.0030371 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137285 | CTGATCTGTCCGGGT[C/T]GTCGAAGAGAGGTTT | 377630 |
| rs752473034 | snp | A/C/T | 0.000112057 | 0.00748451 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138590 | AAGCTGTCTTGCCAC[A/C/T]GGAGCCAAATCATCA | 377630 |
| rs752490166 | snp | A/G | 0.000132442 | 0.00813654 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138558 | CTGCTACTCAGAGGA[A/G]GCTTCTTCCTGGGAG | 377630 |
| rs752498409 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140199 | AAATTGTAATGCTGA[C/T]GAAAGTGGACATGTT | 377630 |
| rs752562870 | snp | A/G | 2.40289e-05 | 0.00346611 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137976 | AACGTCTTGGAGGCC[A/G]GCGCCCTCTGGAGAC | 377630 |
| rs752578756 | snp | A/C/G | 2.13879e-05 | 0.00327009 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137945 | GATGAGGACCTTGGC[A/C/G]GAAGTGTGTAAAGTT | 377630 |
| rs752766949 | snp | A/G/T | 0.000147298 | 0.00858075 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137492 | GGCTCTTTCCACCAA[A/G/T]CGCTCGTCCAACTCG | 377630 |
| rs752946852 | snp | C/T | 1.84759e-05 | 0.00303935 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137137 | TGTGTGTGCGTTCAC[C/T]CCTACGTGTGGGTCG | 377630 |
| rs752949096 | snp | C/T | 2.96274e-05 | 0.00384875 | stop-gained, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137778 | CCGTCGTGACAACTC[C/T]ACCCAGCGTGGACCA | 377630 |
| rs752999441 | snp | C/T | 0.000213321 | 0.0103255 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138484 | GGCACTGCAGGGAAG[C/T]GTTCTCGTAGCAGGT | 377630 |
| rs753243464 | snp | C/T | 5.21553e-05 | 0.00510636 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138682 | TTTCAGCAAAAGCTG[C/T]ATCTGGCCGAGAAGA | 377630 |
| rs753329655 | snp | G/T | 5.88045e-05 | 0.00542207 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138284 | AAATTCATGGGCATC[G/T]TCCTGCTTGCCTCTA | 377630 |
| rs753339318 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140095 | TGTATCTCCTGGATT[C/G]TCGCATCGGTTGTTC | 377630 |
| rs753432029 | snp | A/C | 3.38152e-05 | 0.00411175 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138720 | TTTGAAAAGTGGTTG[A/C]ACTGCCACTCACCTC | 377630 |
| rs753476150 | snp | C/T | 4.03266e-05 | 0.00449018 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137637 | CTTTCCCATTCACTC[C/T]TCTGGATGTAAAAGA | 377630 |
| rs753564542 | snp | A/G | 0.000126723 | 0.00795899 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137678 | CTGTTGACTCAGGAC[A/G]GAAGTGATGCTACAG | 377630 |
| rs753663891 | snp | G/T | 1.84344e-05 | 0.00303593 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137241 | GTCCTCCCTTGCAGA[G/T]AAGCGAGGGTGCCAG | 377630 |
| rs753753772 | snp | G/T | 3.68922e-05 | 0.00429473 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137278 | CGGACTCCTGATCTG[G/T]CCGGGTCGTCGAAGA | 377630 |
| rs753826793 | snp | C/T | 1.90729e-05 | 0.00308805 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138550 | CAGGTCTCCTGCTAC[C/T]CAGAGGAAGCTTCTT | 377630 |
| rs753912338 | snp | C/T | 2.13664e-05 | 0.00326845 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137939 | GACAAGGATGAGGAC[C/T]TTGGCAGAAGTGTGT | 377630 |
| rs753986027 | snp | G/T | 1.83802e-05 | 0.00303146 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137515 | CCAACTCGGGTGCCT[G/T]GAGGCAGGGGTGGTC | 377630 |
| rs754003598 | snp | C/T | 6.60713e-05 | 0.00574728 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137974 | TTAACGTCTTGGAGG[C/T]CGGCGCCCTCTGGAG | 377630 |
| rs754065570 | snp | C/G | 0.000697668 | 0.0186641 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138775 | TGTCGCCCGCAACAA[C/G]GATCACAAGGTTTTT | 377630 |
| rs754247641 | snp | A/G | | | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136887 | CAGTGAATGTCATCT[A/G]CCATGAACACAAACA | 377630 |
| rs754358009 | snp | A/G | 5.57693e-05 | 0.0052803 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137771 | GTAATGTCCGTCGTG[A/G]CAACTCCACCCAGCG | 377630 |
| rs754584437 | snp | C/T | 8.04101e-05 | 0.00634024 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137639 | TTCCCATTCACTCTT[C/T]TGGATGTAAAAGAGG | 377630 |
| rs754594194 | in-del | -/TG | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139208 | GTGTGTGTGTGTTTG[-/TG]TGTGTGTGTGTGTGT | 377630 |
| rs754599841 | snp | G/T | 1.80869e-05 | 0.00300718 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137679 | TGTTGACTCAGGACA[G/T]AAGTGATGCTACAGG | 377630 |
| rs754629865 | snp | C/G/T | 3.68917e-05 | 0.00429473 | synonymous-codon, missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137192 | CACAAGCAGAGCCCT[C/G/T]TTGCTGTGTTTGTTC | 377630 |
| rs754881142 | snp | C/G | 9.52553e-05 | 0.00690062 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138551 | AGGTCTCCTGCTACT[C/G]AGAGGAAGCTTCTTC | 377630 |
| rs754896939 | snp | C/T | 2.12709e-05 | 0.00326114 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137921 | ATCGGAGAATCTCTT[C/T]AAGACAAGGATGAGG | 377630 |
| rs754964080 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140100 | CTCCTGGATTCTCGC[A/T]TCGGTTGTTCATGCT | 377630 |
| rs754989828 | snp | A/G | 2.13979e-05 | 0.00327086 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137943 | AGGATGAGGACCTTG[A/G]CAGAAGTGTGTAAAG | 377630 |
| rs755048119 | snp | A/G | 0.00010561 | 0.00726592 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138740 | CCACTCACCTCCCAA[A/G]TAGAGTGAGTCGTCC | 377630 |
| rs755260103 | snp | G/T | 3.88478e-05 | 0.00440708 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138399 | CAGAGCATGCAGCAC[G/T]TGGGACGCTGACATG | 377630 |
| rs755279564 | snp | A/C/G | 0.000153 | 0.00874533 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138442 | CCCGGGACAGCATGT[A/C/G]GTTGGCAAGGGGCGG | 377630 |
| rs755449591 | snp | A/T | 1.84483e-05 | 0.00303707 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137290 | CTGTCCGGGTCGTCG[A/T]AGAGAGGTTTAGCAG | 377630 |
| rs755479755 | snp | G/T | 1.87054e-05 | 0.00305816 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138611 | CAAATCATCACAGAG[G/T]TCGACACGGGCCTCA | 377630 |
| rs755557006 | snp | A/C | 1.84575e-05 | 0.00303783 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137356 | CACACTTGTATTTCG[A/C]TTGATGAATCACAAG | 377630 |
| rs755636865 | snp | A/C/G | 0.00141981 | 0.0266066 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138637 | CCTCAGATGAGAGTG[A/C/G]TGACTTCTCAGGGAG | 377630 |
| rs755646053 | snp | A/G | 1.84606e-05 | 0.00303808 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137388 | ACGTTGGGAGGCAGG[A/G]TACCTTCGACTTTTC | 377630 |
| rs755701378 | snp | G/T | | | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138037 | TGAGTTCTTCGGGCT[G/T]CACCAACTGTTCCAA | 377630 |
| rs755839704 | snp | A/G | 7.38648e-05 | 0.00607675 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137147 | TTCACCCCTACGTGT[A/G]GGTCGGCACTTCCAC | 377630 |
| rs755873775 | snp | A/C | 2.03411e-05 | 0.00318907 | stop-gained, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137632 | TGTGTCTTTCCCATT[A/C]ACTCTTCTGGATGTA | 377630 |
| rs756002885 | snp | A/T | 1.8447e-05 | 0.00303696 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137186 | CTGGCACACAAGCAG[A/T]GCCCTCTTGCTGTGT | 377630 |
| rs756218767 | snp | A/G | 1.84449e-05 | 0.00303679 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137453 | TTGGGGGAATTTCCA[A/G]TGGTCTAAGGTGCTT | 377630 |
| rs756387995 | snp | A/C | 3.44632e-05 | 0.00415095 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138731 | GTTGAACTGCCACTC[A/C]CCTCCCAAGTAGAGT | 377630 |
| rs756475832 | snp | C/T | 2.24183e-05 | 0.00334793 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138349 | TGACATGACCAGGAC[C/T]GTGGAGGGCCCATGT | 377630 |
| rs756610031 | snp | A/T | 1.78793e-05 | 0.00298987 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137692 | CAGAAGTGATGCTAC[A/T]GGCAGTGACCTTGGC | 377630 |
| rs756714471 | snp | A/G | 1.83427e-05 | 0.00302837 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137729 | CATTTTATACCACTG[A/G]CCTTCTTGAGCTTTG | 377630 |
| rs756802111 | snp | A/C/G/T | 0.000202953 | 0.0100718 | missense, stop-gained, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137289 | TCTGTCCGGGTCGTC[A/C/G/T]AAGAGAGGTTTAGCA | 377630 |
| rs756836047 | snp | A/G | 5.6069e-05 | 0.00529446 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138602 | CACAGGAGCCAAATC[A/G]TCACAGAGGTCGACA | 377630 |
| rs756921830 | snp | C/G | 2.43602e-05 | 0.00348992 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137980 | TCTTGGAGGCCGGCG[C/G]CCTCTGGAGACAAAG | 377630 |
| rs756923976 | snp | A/G | 1.90141e-05 | 0.00308329 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138632 | ACGGGCCTCAGATGA[A/G]AGTGGTGACTTCTCA | 377630 |
| rs756949529 | snp | C/T | | | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137064 | AGGATTGACGGTGTT[C/T]GTGTTTGTGTGTGTG | 377630 |
| rs757013619 | snp | A/G | 9.36067e-05 | 0.00684066 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138034 | CATTGAGTTCTTCGG[A/G]CTTCACCAACTGTTC | 377630 |
| rs757231952 | snp | C/T | 0.000276776 | 0.0117606 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137175 | CACTGAGATCACTGG[C/T]ACACAAGCAGAGCCC | 377630 |
| rs757235735 | snp | A/C | 3.69495e-05 | 0.00429806 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137142 | GTGCGTTCACCCCTA[A/C]GTGTGGGTCGGCACT | 377630 |
| rs757272922 | in-del | -/TGGTCCTCCCTTGCAGAGAAGCGAGGGTGCCAG | 3.68796e-05 | 0.004294 | cds-indel, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137224 | TCCCTTTGGATCTCC[lengthTooLong]TGTTCACGGACTCCT | 377630 |
| rs757391344 | snp | A/T | 2.98245e-05 | 0.00386152 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137863 | GCTGCATGTCAAGGC[A/T]CTCAGGATATTGCAC | 377630 |
| rs757511668 | snp | C/T | 6.47019e-05 | 0.00568742 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137900 | GGCAAGTTTGTTGCC[C/T]GTGACATCGGAGAAT | 377630 |
| rs757680711 | snp | C/G/T | 6.0245e-05 | 0.00548813 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138688 | CAAAAGCTGCATCTG[C/G/T]CCGAGAAGATGTGAG | 377630 |
| rs757768512 | snp | G/T | 3.42742e-05 | 0.00413955 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138729 | TGGTTGAACTGCCAC[G/T]CACCTCCCAAGTAGA | 377630 |
| rs757894045 | snp | C/T | 1.79322e-05 | 0.00299429 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137688 | AGGACAGAAGTGATG[C/T]TACAGGCAGTGACCT | 377630 |
| rs757901839 | snp | A/G | 1.8013e-05 | 0.00300103 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137720 | GGCATCATCCATTTT[A/G]TACCACTGGCCTTCT | 377630 |
| rs758016312 | snp | A/G/T | 0.000208059 | 0.0101976 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138559 | TGCTACTCAGAGGAA[A/G/T]CTTCTTCCTGGGAGC | 377630 |
| rs758278792 | snp | A/G | 2.40538e-05 | 0.0034679 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137977 | ACGTCTTGGAGGCCG[A/G]CGCCCTCTGGAGACA | 377630 |
| rs758405694 | snp | C/T | 0.000119239 | 0.00772045 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138794 | CACAAGGTTTTTCTG[C/T]TGGGACTGCAGGTTG | 377630 |
| rs758421226 | snp | A/G/T | 7.34988e-05 | 0.00606175 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137524 | GTGCCTGGAGGCAGG[A/G/T]GTGGTCTCTCTTGAG | 377630 |
| rs758551478 | snp | A/G | | | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138447 | GACAGCATGTAGTTG[A/G]CAAGGGGCGGTGTGT | 377630 |
| rs758593779 | snp | C/G | 1.8478e-05 | 0.00303951 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137138 | GTGTGTGCGTTCACC[C/G]CTACGTGTGGGTCGG | 377630 |
| rs758640415 | snp | A/G | 3.07243e-05 | 0.00391934 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137783 | GTGACAACTCCACCC[A/G]GCGTGGACCAGCACA | 377630 |
| rs758655715 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139804 | TTATTAAAGAACTGA[C/T]GAAAATAAAAACAAC | 377630 |
| rs758730042 | snp | A/G | 3.65317e-05 | 0.0042737 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137855 | CATGTATGGCTGCAT[A/G]TCAAGGCACTCAGGA | 377630 |
| rs758860795 | snp | C/G | 0.00333889 | 0.0407222 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138066 | AAAGCTTGCTTGACA[C/G]TCTGAGCTGCCTGGA | 377630 |
| rs758921561 | snp | A/T | 0.000154413 | 0.00878538 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138640 | CAGATGAGAGTGGTG[A/T]CTTCTCAGGGAGAGA | 377630 |
| rs759007772 | snp | C/G | 0.000303712 | 0.0123192 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138685 | CAGCAAAAGCTGCAT[C/G]TGGCCGAGAAGATGT | 377630 |
| rs759091655 | snp | A/C | 3.41326e-05 | 0.004131 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138721 | TTGAAAAGTGGTTGA[A/C]CTGCCACTCACCTCC | 377630 |
| rs759207951 | snp | G/T | 4.04801e-05 | 0.00449871 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138420 | CGCTGACATGTTTGA[G/T]AGTGCTCCCGGGACA | 377630 |
| rs759297935 | snp | A/G | 9.30605e-05 | 0.00682067 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137750 | TTGAGCTTTGACATA[A/G]GAGAAGTAATGTCCG | 377630 |
| rs759334105 | snp | A/C | 1.79503e-05 | 0.0029958 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137713 | TGACCTTGGCATCAT[A/C]CATTTTATACCACTG | 377630 |
| rs759745852 | snp | G/T | 0.000144728 | 0.00850548 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138009 | AGACCGCAATGATAG[G/T]CATTCTCTCCATTGA | 377630 |
| rs759929049 | snp | C/T | 1.91049e-05 | 0.00309065 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137584 | CTTCAGCGCCGAGGG[C/T]TCTTGGTTCCCTGCC | 377630 |
| rs760004549 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139325 | CGCTTTCTGACCTGA[A/G]AATAGTCAATGAAGT | 377630 |
| rs760052612 | snp | A/G | 3.86817e-05 | 0.00439765 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138500 | GTTCTCGTAGCAGGT[A/G]TTTCCCATATTCTGG | 377630 |
| rs760061157 | in-del | -/GACGCT | 4.82021e-05 | 0.00490904 | cds-indel, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138403 | GCATGCAGCACTTGG[-/GACGCT]GACATGTTTGAGAGT | 377630 |
| rs760062384 | snp | A/G | 2.26837e-05 | 0.00336769 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137888 | TTGCACATTCTTGGC[A/G]AGTTTGTTGCCTGTG | 377630 |
| rs760152249 | snp | C/T | 0.000406624 | 0.014253 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137437 | TCGTTTTGTTTTGCT[C/T]TTGGGGGAATTTCCA | 377630 |
| rs760179207 | snp | A/C | 2.24183e-05 | 0.00334793 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138674 | CCGCTGGATTTCAGC[A/C]AAAGCTGCATCTGGC | 377630 |
| rs760288256 | in-del | -/CA | | | frameshift-variant, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138038 | GAGTTCTTCGGGCTT[-/CA]CCAACTGTTCCAAAG | 377630 |
| rs760309639 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140612 | GTTCCCCAGAAACAT[A/G]AGCAATCCAGATGCC | 377630 |
| rs760370198 | snp | C/G | 5.53021e-05 | 0.00525814 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137473 | CTAAGGTGCTTTCCT[C/G]AGTGGCTCTTTCCAC | 377630 |
| rs760402589 | snp | A/G | 0.000101394 | 0.00711947 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138716 | GAGTTTTGAAAAGTG[A/G]TTGAACTGCCACTCA | 377630 |
| rs760432754 | snp | A/G | 2.49299e-05 | 0.00353048 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138318 | AAGCCAGCAGCCAAT[A/G]CCTGTGAGGGCTGGA | 377630 |
| rs760446794 | snp | A/T | 2.30226e-05 | 0.00339276 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138371 | GGCCCATGTGATGTG[A/T]GCTTGCATAGTACAG | 377630 |
| rs760523107 | snp | A/G | 1.81912e-05 | 0.00301584 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137675 | GGCCTGTTGACTCAG[A/G]ACAGAAGTGATGCTA | 377630 |
| rs760540989 | snp | C/G | 9.21837e-05 | 0.00678847 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137233 | ATCTCCTGGTCCTCC[C/G]TTGCAGAGAAGCGAG | 377630 |
| rs760610896 | snp | A/G | 7.14669e-05 | 0.00597732 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137706 | CAGGCAGTGACCTTG[A/G]CATCATCCATTTTAT | 377630 |
| rs760618378 | in-del | -/G | 3.76074e-05 | 0.00433616 | frameshift-variant, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138569 | AGGAAGCTTCTTCCT[-/G]GGAGCAAGCTGTCTT | 377630 |
| rs760767778 | snp | C/G | 1.84422e-05 | 0.00303657 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137272 | TGTTCACGGACTCCT[C/G]ATCTGTCCGGGTCGT | 377630 |
| rs760816302 | snp | C/T | 1.92003e-05 | 0.00309835 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138542 | CACCGCAGCAGGTCT[C/T]CTGCTACTCAGAGGA | 377630 |
| rs760821633 | snp | G/T | 3.64884e-05 | 0.00427117 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137972 | AGTTAACGTCTTGGA[G/T]GCCGGCGCCCTCTGG | 377630 |
| rs760909635 | snp | A/C | 3.67607e-05 | 0.00428707 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137512 | CGTCCAACTCGGGTG[A/C]CTGGAGGCAGGGGTG | 377630 |
| rs760913831 | snp | A/G | | | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136880 | AAATACACAGTGAAT[A/G]TCATCTACCATGAAC | 377630 |
| rs761104834 | in-del | -/TG | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139207 | GTGTGTGTGTGTGTT[-/TG]TGTGTGTGTGTGTGT | 377630 |
| rs761150922 | snp | C/T | 9.18721e-05 | 0.00677699 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137549 | CTTGAGCTCTCCTTG[C/T]GTTGCTCGCCTGTCT | 377630 |
| rs761156535 | snp | A/G | 7.39331e-05 | 0.00607956 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137131 | CGTGTGTGTGTGTGC[A/G]TTCACCCCTACGTGT | 377630 |
| rs761198369 | snp | C/T | 1.9477e-05 | 0.0031206 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138471 | GGTGTGTATGTCAGG[C/T]ACTGCAGGGAAGCGT | 377630 |
| rs761267593 | snp | A/G | 1.81893e-05 | 0.00301568 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138436 | AGTGCTCCCGGGACA[A/G]CATGTAGTTGGCAAG | 377630 |
| rs761471078 | snp | G/T | 4.55633e-05 | 0.00477279 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137821 | GGACATAGACAAGAG[G/T]TCCTGTGTTCTGCTG | 377630 |
| rs761564697 | snp | A/G | 1.84602e-05 | 0.00303805 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137386 | GTACGTTGGGAGGCA[A/G]GGTACCTTCGACTTT | 377630 |
| rs761663470 | snp | A/G | 3.32607e-05 | 0.0040779 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138709 | AAGATGTGAGTTTTG[A/G]AAAGTGGTTGAACTG | 377630 |
| rs761674527 | snp | C/T | 2.00632e-05 | 0.00316721 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137612 | GCCTCTTGACACACT[C/T]TCACTGTGTCTTTCC | 377630 |
| rs761952726 | snp | A/G | 1.92918e-05 | 0.00310572 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138534 | CCAGCCCCCACCGCA[A/G]CAGGTCTCCTGCTAC | 377630 |
| rs761990786 | snp | C/G | | | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137223 | TTCCCTTTGGATCTC[C/G]TGGTCCTCCCTTGCA | 377630 |
| rs762017750 | snp | A/C/G | 5.79832e-05 | 0.00538412 | synonymous-codon, missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138509 | GCAGGTATTTCCCAT[A/C/G]TTCTGGAGCCCAGCC | 377630 |
| rs762040648 | snp | G/T | 4.26876e-05 | 0.00461974 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137933 | CTTCAAGACAAGGAT[G/T]AGGACCTTGGCAGAA | 377630 |
| rs762227934 | snp | A/C | 9.20887e-05 | 0.00678497 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137488 | GAGTGGCTCTTTCCA[A/C]CAAGCGCTCGTCCAA | 377630 |
| rs762316025 | snp | G/T | 3.49901e-05 | 0.00418256 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137510 | CTCGTCCAACTCGGG[G/T]GCCTGGAGGCAGGGG | 377630 |
| rs762338845 | snp | C/T | 4.03722e-05 | 0.00449272 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138810 | TGGGACTGCAGGTTG[C/T]AGCAAGACGCTATCT | 377630 |
| rs762517355 | snp | A/G | 2.41461e-05 | 0.00347455 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138385 | GAGCTTGCATAGTAC[A/G]GAGCATGCAGCACTT | 377630 |
| rs762696686 | snp | C/T | 5.83289e-05 | 0.0054001 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137760 | ACATAAGAGAAGTAA[C/T]GTCCGTCGTGACAAC | 377630 |
| rs762722707 | snp | A/C/T | 5.64332e-05 | 0.00531168 | synonymous-codon, missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138623 | GAGGTCGACACGGGC[A/C/T]TCAGATGAGAGTGGT | 377630 |
| rs762799127 | snp | G/T | 3.69768e-05 | 0.00429965 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137811 | ACAGCATAGAGGACA[G/T]AGACAAGAGGTCCTG | 377630 |
| rs762807200 | snp | A/T | 4.26267e-05 | 0.00461644 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138020 | ATAGGCATTCTCTCC[A/T]TTGAGTTCTTCGGGC | 377630 |
| rs762961738 | snp | C/T | 6.23435e-05 | 0.00558282 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138660 | TCAGGGAGAGAAGTC[C/T]GCTGGATTTCAGCAA | 377630 |
| rs763172737 | snp | C/T | 1.93669e-05 | 0.00311176 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137595 | AGGGCTCTTGGTTCC[C/T]TGCCTCTTGACACAC | 377630 |
| rs763259750 | snp | A/G | 3.80019e-05 | 0.00435884 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137660 | GTAAAAGAGGACATA[A/G]GCCTGTTGACTCAGG | 377630 |
| rs763347972 | snp | C/T | 1.84446e-05 | 0.00303677 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137212 | TGTGTTTGTTCTTCC[C/T]TTTGGATCTCCTGGT | 377630 |
| rs763365119 | snp | C/T | 2.21545e-05 | 0.00332818 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137893 | CATTCTTGGCAAGTT[C/T]GTTGCCTGTGACATC | 377630 |
| rs763365314 | snp | C/T | 0.000135327 | 0.00822467 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138530 | GAGCCCAGCCCCCAC[C/T]GCAGCAGGTCTCCTG | 377630 |
| rs763452336 | snp | A/C/G/T | 0.000106674 | 0.0073026 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137932 | TCTTCAAGACAAGGA[A/C/G/T]GAGGACCTTGGCAGA | 377630 |
| rs763689364 | snp | A/C | 3.61945e-05 | 0.00425393 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137723 | ATCATCCATTTTATA[A/C]CACTGGCCTTCTTGA | 377630 |
| rs763791041 | snp | C/T | 1.86771e-05 | 0.00305585 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138595 | GTCTTGCCACAGGAG[C/T]CAAATCATCACAGAG | 377630 |
| rs763939139 | snp | C/G/T | 3.69217e-05 | 0.00429648 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137384 | AAGTACGTTGGGAGG[C/G/T]AGGGTACCTTCGACT | 377630 |
| rs764040872 | snp | C/T | 4.94303e-05 | 0.00497119 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138021 | TAGGCATTCTCTCCA[C/T]TGAGTTCTTCGGGCT | 377630 |
| rs764358418 | snp | C/T | 1.84538e-05 | 0.00303752 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137171 | CTTCCACTGAGATCA[C/T]TGGCACACAAGCAGA | 377630 |
| rs764424620 | snp | C/T | 9.66791e-05 | 0.00695199 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138506 | GTAGCAGGTATTTCC[C/T]ATATTCTGGAGCCCA | 377630 |
| rs764433699 | snp | A/G | 4.39174e-05 | 0.00468581 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137897 | CTTGGCAAGTTTGTT[A/G]CCTGTGACATCGGAG | 377630 |
| rs764436722 | in-del | -/A | 3.73591e-05 | 0.00432182 | frameshift-variant, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138588 | GCAAGCTGTCTTGCC[-/A]CAGGAGCCAAATCAT | 377630 |
| rs764525312 | snp | C/G | 1.84834e-05 | 0.00303996 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137443 | TGTTTTGCTCTTGGG[C/G]GAATTTCCAGTGGTC | 377630 |
| rs764613515 | snp | C/T | 1.84255e-05 | 0.0030352 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137480 | GCTTTCCTGAGTGGC[C/T]CTTTCCACCAAGCGC | 377630 |
| rs764753017 | snp | A/C | 0.00017099 | 0.00924477 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138727 | AGTGGTTGAACTGCC[A/C]CTCACCTCCCAAGTA | 377630 |
| rs764837008 | snp | C/T | 1.79503e-05 | 0.0029958 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137714 | GACCTTGGCATCATC[C/T]ATTTTATACCACTGG | 377630 |
| rs764894876 | snp | A/G | 5.41492e-05 | 0.00520304 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137681 | TTGACTCAGGACAGA[A/G]GTGATGCTACAGGCA | 377630 |
| rs765013265 | snp | A/G | 3.68983e-05 | 0.00429509 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137281 | ACTCCTGATCTGTCC[A/G]GGTCGTCGAAGAGAG | 377630 |
| rs765134057 | snp | A/G | 5.62783e-05 | 0.00530434 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138619 | CACAGAGGTCGACAC[A/G]GGCCTCAGATGAGAG | 377630 |
| rs765177830 | snp | A/G | 1.86788e-05 | 0.00305599 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138588 | GCAAGCTGTCTTGCC[A/G]CAGGAGCCAAATCAT | 377630 |
| rs765402907 | snp | A/C/T | 0.000321059 | 0.0126663 | missense, stop-gained, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138019 | GATAGGCATTCTCTC[A/C/T]ATTGAGTTCTTCGGG | 377630 |
| rs765490748 | snp | A/T | 0.000221468 | 0.0105207 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137165 | TCGGCACTTCCACTG[A/T]GATCACTGGCACACA | 377630 |
| rs765593814 | snp | A/C | 1.93939e-05 | 0.00311394 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138481 | TCAGGCACTGCAGGG[A/C]AGCGTTCTCGTAGCA | 377630 |
| rs765679707 | in-del | -/C | 0.000168103 | 0.00916641 | frameshift-variant, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138448 | ACAGCATGTAGTTGG[-/C]AAGGGGCGGTGTGTA | 377630 |
| rs765703914 | snp | G/T | 1.84582e-05 | 0.00303789 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137389 | CGTTGGGAGGCAGGG[G/T]ACCTTCGACTTTTCT | 377630 |
| rs765747874 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139332 | TGACCTGAGAATAGT[C/G]AATGAAGTATAGTAT | 377630 |
| rs765845032 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140091 | ACCGTGTATCTCCTG[G/T]ATTCTCGCATCGGTT | 377630 |
| rs765899421 | snp | A/G/T | 5.54609e-05 | 0.00526573 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137441 | TTTGTTTTGCTCTTG[A/G/T]GGGAATTTCCAGTGG | 377630 |
| rs765910465 | snp | A/G | 3.39127e-05 | 0.00411767 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138719 | TTTTGAAAAGTGGTT[A/G]AACTGCCACTCACCT | 377630 |
| rs765930815 | snp | A/G | 2.45468e-05 | 0.00350326 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138678 | TGGATTTCAGCAAAA[A/G]CTGCATCTGGCCGAG | 377630 |
| rs765997816 | snp | C/T | 2.38163e-05 | 0.00345074 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138323 | AGCAGCCAATGCCTG[C/T]GAGGGCTGGATGACA | 377630 |
| rs766015132 | snp | C/T | 6.13779e-05 | 0.00553942 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138283 | GAAATTCATGGGCAT[C/T]TTCCTGCTTGCCTCT | 377630 |
| rs766158696 | snp | A/G | 1.81648e-05 | 0.00301365 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137676 | GCCTGTTGACTCAGG[A/G]CAGAAGTGATGCTAC | 377630 |
| rs766236916 | snp | C/T | 1.84384e-05 | 0.00303626 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137234 | TCTCCTGGTCCTCCC[C/T]TGCAGAGAAGCGAGG | 377630 |
| rs766245208 | snp | A/C/T | 8.95606e-05 | 0.00669128 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137712 | GTGACCTTGGCATCA[A/C/T]CCATTTTATACCACT | 377630 |
| rs766326732 | snp | A/T | 1.84429e-05 | 0.00303663 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137274 | TTCACGGACTCCTGA[A/T]CTGTCCGGGTCGTCG | 377630 |
| rs766482332 | snp | C/G | 0.000114583 | 0.00756823 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138549 | GCAGGTCTCCTGCTA[C/G]TCAGAGGAAGCTTCT | 377630 |
| rs766574391 | snp | A/C | 2.13554e-05 | 0.00326761 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137938 | AGACAAGGATGAGGA[A/C]CTTGGCAGAAGTGTG | 377630 |
| rs766660169 | snp | A/G | 4.38904e-05 | 0.00468437 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137973 | GTTAACGTCTTGGAG[A/G]CCGGCGCCCTCTGGA | 377630 |
| rs766665748 | snp | C/G | 1.83778e-05 | 0.00303126 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137513 | GTCCAACTCGGGTGC[C/G]TGGAGGCAGGGGTGG | 377630 |
| rs766738573 | snp | G/T | 1.84776e-05 | 0.00303949 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137133 | TGTGTGTGTGTGCGT[G/T]CACCCCTACGTGTGG | 377630 |
| rs766756954 | snp | A/C | 2.34074e-05 | 0.00342099 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138437 | GTGCTCCCGGGACAG[A/C]ATGTAGTTGGCAAGG | 377630 |
| rs766963813 | snp | C/T | 1.94369e-05 | 0.00311738 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138476 | GTATGTCAGGCACTG[C/T]AGGGAAGCGTTCTCG | 377630 |
| rs767049999 | snp | C/T | 1.96207e-05 | 0.00313209 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137831 | AAGAGGTCCTGTGTT[C/T]TGCTGAGACATGTAT | 377630 |
| rs767064592 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139481 | GGCCAGTGGAGAACA[A/G]GACAAGTCTTTGCAT | 377630 |
| rs767126683 | snp | C/T | 1.82387e-05 | 0.00301977 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138635 | GGCCTCAGATGAGAG[C/T]GGTGACTTCTCAGGG | 377630 |
| rs767216701 | snp | A/C | 2.09019e-05 | 0.00323273 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138662 | AGGGAGAGAAGTCCG[A/C]TGGATTTCAGCAAAA | 377630 |
| rs767218383 | snp | A/C | 9.56617e-05 | 0.00691532 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138035 | ATTGAGTTCTTCGGG[A/C]TTCACCAACTGTTCC | 377630 |
| rs767223033 | snp | A/G/T | 0.000129207 | 0.00803674 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137387 | TACGTTGGGAGGCAG[A/G/T]GTACCTTCGACTTTT | 377630 |
| rs767306650 | snp | C/G | 5.83448e-05 | 0.00540083 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138266 | ATCCACAGTGAACAT[C/G]AGAAATTCATGGGCA | 377630 |
| rs767318316 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139443 | CGTTCAGCCTATTGA[C/T]TCTCTATCCGAGTGA | 377630 |
| rs767398230 | snp | A/G | 2.53682e-05 | 0.00356138 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138316 | GGAAGCCAGCAGCCA[A/G]TGCCTGTGAGGGCTG | 377630 |
| rs767487911 | snp | A/C/G | 5.53126e-05 | 0.00525868 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137228 | TTTGGATCTCCTGGT[A/C/G]CTCCCTTGCAGAGAA | 377630 |
| rs767536422 | snp | C/G | 1.84517e-05 | 0.00303735 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137177 | CTGAGATCACTGGCA[C/G]ACAAGCAGAGCCCTC | 377630 |
| rs767583306 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140729 | AGGTGAGCCGAATTG[A/C]TGTCCTGCCTGCGTG | 377630 |
| rs767583659 | snp | C/T | 0.000234209 | 0.010819 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137908 | TGTTGCCTGTGACAT[C/T]GGAGAATCTCTTCAA | 377630 |
| rs767872344 | snp | C/T | 4.40694e-05 | 0.0046939 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138763 | AGTCGTCCTCCATGT[C/T]GCCCGCAACAAGGAT | 377630 |
| rs767957085 | snp | A/G/T | 7.35232e-05 | 0.00606275 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137511 | TCGTCCAACTCGGGT[A/G/T]CCTGGAGGCAGGGGT | 377630 |
| rs768117467 | snp | A/G | 6.00426e-05 | 0.00547884 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138811 | GGGACTGCAGGTTGC[A/G]GCAAGACGCTATCTC | 377630 |
| rs768122288 | snp | A/G | 3.69638e-05 | 0.0042989 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137129 | TGCGTGTGTGTGTGT[A/G]CGTTCACCCCTACGT | 377630 |
| rs768184340 | snp | A/G | 2.46825e-05 | 0.00351293 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138388 | CTTGCATAGTACAGA[A/G]CATGCAGCACTTGGG | 377630 |
| rs768414142 | snp | A/T | 1.84769e-05 | 0.00303943 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137415 | TTTCTGACGTTGAAC[A/T]CAGGCTTCGTTTTGT | 377630 |
| rs768466333 | snp | A/G | 1.85575e-05 | 0.00304605 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137813 | AGCATAGAGGACATA[A/G]ACAAGAGGTCCTGTG | 377630 |
| rs768630139 | snp | G/T | 0.000449121 | 0.0149786 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138696 | GCATCTGGCCGAGAA[G/T]ATGTGAGTTTTGAAA | 377630 |
| rs768663169 | snp | A/C | 3.68922e-05 | 0.00429473 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137461 | ATTTCCAGTGGTCTA[A/C]GGTGCTTTCCTGAGT | 377630 |
| rs768674212 | in-del | -/AGTG | 8.92833e-05 | 0.00668084 | frameshift-variant, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137695 | AGTGATGCTACAGGC[-/AGTG]AGTGACCTTGGCATC | 377630 |
| rs768706489 | snp | A/T | 6.77254e-05 | 0.00581877 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138354 | TGACCAGGACTGTGG[A/T]GGGCCCATGTGATGT | 377630 |
| rs768794438 | snp | A/C | 3.57152e-05 | 0.00422568 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137695 | AAGTGATGCTACAGG[A/C]AGTGACCTTGGCATC | 377630 |
| rs768869247 | snp | A/T | | | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136684 | CTATCTTCTAAATGC[A/T]TTCCAGTTTCCACTA | 377630 |
| rs769017865 | snp | G/T | 1.84388e-05 | 0.00303629 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137217 | TTGTTCTTCCCTTTG[G/T]ATCTCCTGGTCCTCC | 377630 |
| rs769107772 | snp | A/T | 1.8433e-05 | 0.00303581 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137259 | GCGAGGGTGCCAGTG[A/T]TCACGGACTCCTGAT | 377630 |
| rs769282150 | snp | C/G | 9.9005e-05 | 0.0070351 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137984 | GGAGGCCGGCGCCCT[C/G]TGGAGACAAAGACCG | 377630 |
| rs769374031 | snp | A/C | 1.83687e-05 | 0.00303051 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137532 | AGGCAGGGGTGGTCT[A/C]TCTTGAGCTCTCCTT | 377630 |
| rs769520632 | snp | C/T | 0.000118984 | 0.00771218 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138803 | TTTCTGCTGGGACTG[C/T]AGGTTGCAGCAAGAC | 377630 |
| rs769549194 | snp | A/T | 3.65397e-05 | 0.00427417 | stop-gained, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137801 | GTGGACCAGCACAGC[A/T]TAGAGGACATAGACA | 377630 |
| rs769610822 | snp | A/T | 3.79918e-05 | 0.00435826 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138423 | TGACATGTTTGAGAG[A/T]GCTCCCGGGACAGCA | 377630 |
| rs769613745 | snp | A/G | 3.76974e-05 | 0.00434135 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137755 | CTTTGACATAAGAGA[A/G]GTAATGTCCGTCGTG | 377630 |
| rs769697053 | snp | G/T | 1.96609e-05 | 0.00313529 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138457 | AGTTGGCAAGGGGCG[G/T]TGTGTATGTCAGGCA | 377630 |
| rs769909130 | snp | C/G | 4.07623e-05 | 0.00451436 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138654 | GACTTCTCAGGGAGA[C/G]AAGTCCGCTGGATTT | 377630 |
| rs770083218 | snp | A/C | 0.00382408 | 0.0435593 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138211 | CCTTAGAGTGATGAT[A/C]TACCTGCTTGTGGCC | 377630 |
| rs770234887 | snp | C/T | 7.73231e-05 | 0.00621736 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138504 | TCGTAGCAGGTATTT[C/T]CCATATTCTGGAGCC | 377630 |
| rs770321229 | in-del | -/T | 1.86197e-05 | 0.00305115 | frameshift-variant, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138288 | TCATGGGCATCTTCC[-/T]GCTTGCCTCTATGGA | 377630 |
| rs770432787 | snp | A/G | 1.8434e-05 | 0.0030359 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137255 | AGAAGCGAGGGTGCC[A/G]GTGTTCACGGACTCC | 377630 |
| rs770438629 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140400 | ATGGCCCATGAAATT[A/C]GGATGATTTTAAGGA | 377630 |
| rs770546703 | snp | A/G | 6.4268e-05 | 0.00566832 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137957 | GGCAGAAGTGTGTAA[A/G]GTTAACGTCTTGGAG | 377630 |
| rs770669355 | snp | A/C | 3.75467e-05 | 0.00433266 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138751 | CCAAGTAGAGTGAGT[A/C]GTCCTCCATGTCGCC | 377630 |
| rs770753140 | snp | A/G | 2.30396e-05 | 0.00339401 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138372 | GCCCATGTGATGTGA[A/G]CTTGCATAGTACAGA | 377630 |
| rs770975046 | snp | A/G | 0.000309272 | 0.0124314 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137786 | ACAACTCCACCCAGC[A/G]TGGACCAGCACAGCA | 377630 |
| rs771231857 | snp | A/G | 7.49541e-05 | 0.00612139 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138617 | ATCACAGAGGTCGAC[A/G]CGGGCCTCAGATGAG | 377630 |
| rs771401204 | snp | A/G | 1.90221e-05 | 0.00308394 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137581 | TGTCTTCAGCGCCGA[A/G]GGCTCTTGGTTCCCT | 377630 |
| rs771461899 | snp | C/T | 1.84449e-05 | 0.00303679 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137196 | AGCAGAGCCCTCTTG[C/T]TGTGTTTGTTCTTCC | 377630 |
| rs771482220 | snp | G/T | 1.93418e-05 | 0.00310975 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138497 | AGCGTTCTCGTAGCA[G/T]GTATTTCCCATATTC | 377630 |
| rs771501058 | snp | C/T | 3.69201e-05 | 0.00429636 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137159 | TGTGGGTCGGCACTT[C/T]CACTGAGATCACTGG | 377630 |
| rs771568275 | snp | A/G | 1.79338e-05 | 0.00299443 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137885 | ATATTGCACATTCTT[A/G]GCAAGTTTGTTGCCT | 377630 |
| rs771699654 | snp | A/C | 1.93549e-05 | 0.0031108 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138519 | CCCATATTCTGGAGC[A/C]CAGCCCCCACCGCAG | 377630 |
| rs771758746 | in-del | -/T | 2.36919e-05 | 0.00344171 | frameshift-variant, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137883 | GGATATTGCACATTC[-/T]TGGCAAGTTTGTTGC | 377630 |
| rs771858624 | snp | C/G | 7.32306e-05 | 0.00605061 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138745 | CACCTCCCAAGTAGA[C/G]TGAGTCGTCCTCCAT | 377630 |
| rs771971624 | snp | C/T | 3.68759e-05 | 0.00429378 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137466 | CAGTGGTCTAAGGTG[C/T]TTTCCTGAGTGGCTC | 377630 |
| rs772037870 | snp | A/C/T | 9.09184e-05 | 0.00674185 | stop-gained, missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138359 | AGGACTGTGGAGGGC[A/C/T]CATGTGATGTGAGCT | 377630 |
| rs772129539 | snp | A/G | 0.000484004 | 0.0155489 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138406 | TGCAGCACTTGGGAC[A/G]CTGACATGTTTGAGA | 377630 |
| rs772217561 | snp | C/G/T | 0.000387854 | 0.0139206 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137742 | TGGCCTTCTTGAGCT[C/G/T]TGACATAAGAGAAGT | 377630 |
| rs772277926 | snp | A/G | 5.53062e-05 | 0.00525833 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137264 | GGTGCCAGTGTTCAC[A/G]GACTCCTGATCTGTC | 377630 |
| rs772322528 | snp | C/T | 8.6766e-05 | 0.00658601 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137967 | TGTAAAGTTAACGTC[C/T]TGGAGGCCGGCGCCC | 377630 |
| rs772600752 | snp | C/G | 1.83606e-05 | 0.00302984 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137540 | GTGGTCTCTCTTGAG[C/G]TCTCCTTGCGTTGCT | 377630 |
| rs772707717 | snp | C/G | 2.12963e-05 | 0.00326308 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137926 | AGAATCTCTTCAAGA[C/G]AAGGATGAGGACCTT | 377630 |
| rs772714833 | snp | C/T | 0.000116198 | 0.00762138 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138499 | CGTTCTCGTAGCAGG[C/T]ATTTCCCATATTCTG | 377630 |
| rs772732277 | in-del | -/G | 2.13459e-05 | 0.00326687 | frameshift-variant, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137935 | TCAAGACAAGGATGA[-/G]GACCTTGGCAGAAGT | 377630 |
| rs772802715 | snp | A/C | 4.58096e-05 | 0.00478568 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137887 | ATTGCACATTCTTGG[A/C]AAGTTTGTTGCCTGT | 377630 |
| rs772968300 | snp | A/T | 3.69665e-05 | 0.00429906 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137436 | TTCGTTTTGTTTTGC[A/T]CTTGGGGGAATTTCC | 377630 |
| rs773095802 | snp | C/T | 3.69201e-05 | 0.00429636 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138746 | ACCTCCCAAGTAGAG[C/T]GAGTCGTCCTCCATG | 377630 |
| rs773169134 | snp | A/C | 1.84391e-05 | 0.00303632 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137270 | AGTGTTCACGGACTC[A/C]TGATCTGTCCGGGTC | 377630 |
| rs773443983 | snp | G/T | 3.69113e-05 | 0.00429584 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137307 | GAGAGGTTTAGCAGG[G/T]AGCTTTGCTGTTCAG | 377630 |
| rs773472023 | snp | A/C/T | 5.27454e-05 | 0.00513516 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137998 | TCTGGAGACAAAGAC[A/C/T]GCAATGATAGGCATT | 377630 |
| rs773492809 | in-del | -/AAT | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139526 | GAAGCTAGGCTGCCA[-/AAT]AATAAAGCATCAAAT | 377630 |
| rs773564016 | snp | C/T | 1.83683e-05 | 0.00303048 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137545 | CTCTCTTGAGCTCTC[C/T]TTGCGTTGCTCGCCT | 377630 |
| rs773588672 | snp | A/G | 3.96983e-05 | 0.00445506 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138812 | GGACTGCAGGTTGCA[A/G]CAAGACGCTATCTCT | 377630 |
| rs773773695 | snp | C/T | 7.39782e-05 | 0.00608142 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137130 | GCGTGTGTGTGTGTG[C/T]GTTCACCCCTACGTG | 377630 |
| rs773854147 | snp | C/T | 1.93542e-05 | 0.00311074 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138495 | GAAGCGTTCTCGTAG[C/T]AGGTATTTCCCATAT | 377630 |
| rs774129293 | snp | C/T | 3.96157e-05 | 0.00445043 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137815 | CATAGAGGACATAGA[C/T]AAGAGGTCCTGTGTT | 377630 |
| rs774259829 | snp | G/T | 3.32984e-05 | 0.00408021 | stop-gained, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138708 | GAAGATGTGAGTTTT[G/T]AAAAGTGGTTGAACT | 377630 |
| rs774303516 | snp | C/G | 1.84776e-05 | 0.00303949 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137416 | TTCTGACGTTGAACT[C/G]AGGCTTCGTTTTGTT | 377630 |
| rs774320641 | snp | C/T | 3.73972e-05 | 0.00432402 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137664 | AAGAGGACATAGGCC[C/T]GTTGACTCAGGACAG | 377630 |
| rs774321188 | snp | G/T | 0.002574 | 0.0357823 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138249 | CATGCCTTTTTCATG[G/T]CATCCACAGTGAACA | 377630 |
| rs774514716 | snp | A/C | | | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12136688 | CTTCTAAATGCATTC[A/C]AGTTTCCACTATTCA | 377630 |
| rs774689700 | snp | C/T | 9.2199e-05 | 0.00678904 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137222 | CTTCCCTTTGGATCT[C/T]CTGGTCCTCCCTTGC | 377630 |
| rs774699001 | snp | C/T | 1.84333e-05 | 0.00303584 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137261 | GAGGGTGCCAGTGTT[C/T]ACGGACTCCTGATCT | 377630 |
| rs774709275 | snp | A/C | 1.81972e-05 | 0.00301633 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138532 | GCCCAGCCCCCACCG[A/C]AGCAGGTCTCCTGCT | 377630 |
| rs774953200 | snp | C/T | 1.85005e-05 | 0.00304137 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137120 | GTGTATTTGTGCGTG[C/T]GTGTGTGTGCGTTCA | 377630 |
| rs774997041 | snp | C/G | 7.34578e-05 | 0.00605999 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137534 | GCAGGGGTGGTCTCT[C/G]TTGAGCTCTCCTTGC | 377630 |
| rs775067519 | snp | G/T | 1.89102e-05 | 0.00307486 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137757 | TTGACATAAGAGAAG[G/T]AATGTCCGTCGTGAC | 377630 |
| rs775169981 | snp | A/T | 4.52991e-05 | 0.00475894 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138804 | TTCTGCTGGGACTGC[A/T]GGTTGCAGCAAGACG | 377630 |
| rs775348347 | snp | C/G | 1.96073e-05 | 0.00313101 | stop-gained, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138461 | GGCAAGGGGCGGTGT[C/G]TATGTCAGGCACTGC | 377630 |
| rs775364406 | snp | C/G | 6.18882e-05 | 0.0055624 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138659 | CTCAGGGAGAGAAGT[C/G]CGCTGGATTTCAGCA | 377630 |
| rs775365962 | snp | A/G | 3.50736e-05 | 0.00418755 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137805 | ACCAGCACAGCATAG[A/G]GGACATAGACAAGAG | 377630 |
| rs775453808 | snp | A/G/T | 7.38396e-05 | 0.0060758 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137379 | ATCACAAGTACGTTG[A/G/T]GAGGCAGGGTACCTT | 377630 |
| rs775820686 | snp | C/G | 3.84615e-05 | 0.00438512 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137590 | CGCCGAGGGCTCTTG[C/G]TTCCCTGCCTCTTGA | 377630 |
| rs775839609 | in-del | -/CTC | 1.92306e-05 | 0.00310079 | cds-indel, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138540 | CCCACCGCAGCAGGT[-/CTC]CTGCTACTCAGAGGA | 377630 |
| rs775860050 | snp | A/C/T | 3.86587e-05 | 0.00439638 | missense, stop-gained, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138505 | CGTAGCAGGTATTTC[A/C/T]CATATTCTGGAGCCC | 377630 |
| rs775908518 | snp | A/G | 3.81308e-05 | 0.00436623 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137659 | TGTAAAAGAGGACAT[A/G]GGCCTGTTGACTCAG | 377630 |
| rs775924824 | snp | A/G | 5.53705e-05 | 0.00526138 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137166 | CGGCACTTCCACTGA[A/G]ATCACTGGCACACAA | 377630 |
| rs775949965 | snp | C/T | 3.8669e-05 | 0.00439693 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138527 | CTGGAGCCCAGCCCC[C/T]ACCGCAGCAGGTCTC | 377630 |
| rs775954020 | snp | C/T | 4.4606e-05 | 0.0047224 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137891 | CACATTCTTGGCAAG[C/T]TTGTTGCCTGTGACA | 377630 |
| rs776043740 | snp | A/G | 6.39216e-05 | 0.00565303 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137930 | TCTCTTCAAGACAAG[A/G]ATGAGGACCTTGGCA | 377630 |
| rs776055921 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140007 | ACGTTTAAAAGCAGT[A/G]AGTGAAACAGAGGGT | 377630 |
| rs776127919 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140733 | GAGCCGAATTGATGT[C/T]CTGCCTGCGTGTCAT | 377630 |
| rs776221179 | snp | A/G/T | 6.97007e-05 | 0.00590308 | missense, stop-gained, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138376 | ATGTGATGTGAGCTT[A/G/T]CATAGTACAGAGCAT | 377630 |
| rs776503984 | snp | C/T | 0.000125615 | 0.00792412 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138417 | GGACGCTGACATGTT[C/T]GAGAGTGCTCCCGGG | 377630 |
| rs776600304 | snp | A/G | 1.86131e-05 | 0.00305061 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137749 | CTTGAGCTTTGACAT[A/G]AGAGAAGTAATGTCC | 377630 |
| rs776605778 | snp | A/T | 5.53838e-05 | 0.00526202 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137319 | AGGGAGCTTTGCTGT[A/T]CAGGATGATGGTTTT | 377630 |
| rs776833242 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139936 | AAGGAAAATTATACC[A/G]TAGAAAAGCCCGGGT | 377630 |
| rs776955881 | snp | A/G/T | 3.69162e-05 | 0.00429616 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137163 | GGTCGGCACTTCCAC[A/G/T]GAGATCACTGGCACA | 377630 |
| rs776969004 | snp | A/T | 0.00044774 | 0.0149556 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138006 | CAAAGACCGCAATGA[A/T]AGGCATTCTCTCCAT | 377630 |
| rs777058788 | snp | A/G | 0.00317964 | 0.0397456 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138134 | TGAAATCCCGTGGCA[A/G]TGGAGACACTTGATT | 377630 |
| rs777059263 | snp | A/C/G/T | 0.000166282 | 0.00911701 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137136 | GTGTGTGTGCGTTCA[A/C/G/T]CCCTACGTGTGGGTC | 377630 |
| rs777137917 | snp | G/T | 0.000202767 | 0.0100669 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137249 | TTGCAGAGAAGCGAG[G/T]GTGCCAGTGTTCACG | 377630 |
| rs777159850 | in-del | -/GAG | 2.38163e-05 | 0.00345074 | cds-indel, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138323 | GCAGCCAATGCCTGT[-/GAG]GAGGGCTGGATGACA | 377630 |
| rs777312065 | in-del | -/T | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139796 | CTTTTGTTTATTAAA[-/T]GAACTGATGAAAATA | 377630 |
| rs777552660 | snp | G/T | 0.000388777 | 0.0139369 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138796 | CAAGGTTTTTCTGCT[G/T]GGACTGCAGGTTGCA | 377630 |
| rs777713114 | snp | A/C | 1.84011e-05 | 0.00303319 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137500 | CCACCAAGCGCTCGT[A/C]CAACTCGGGTGCCTG | 377630 |
| rs777795560 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139805 | TATTAAAGAACTGAT[C/G]AAAATAAAAACAACG | 377630 |
| rs777840351 | snp | A/C | 2.06026e-05 | 0.0032095 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138449 | CAGCATGTAGTTGGC[A/C]AGGGGCGGTGTGTAT | 377630 |
| rs777904782 | snp | A/C | 3.69249e-05 | 0.00429664 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137367 | TTCGATTGATGAATC[A/C]CAAGTACGTTGGGAG | 377630 |
| rs777930511 | snp | G/T | 0.000123047 | 0.00784271 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137784 | TGACAACTCCACCCA[G/T]CGTGGACCAGCACAG | 377630 |
| rs778018816 | snp | C/T | 6.92473e-05 | 0.00588378 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137857 | TGTATGGCTGCATGT[C/T]AAGGCACTCAGGATA | 377630 |
| rs778289547 | snp | C/T | 5.96902e-05 | 0.00546274 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137644 | ATTCACTCTTCTGGA[C/T]GTAAAAGAGGACATA | 377630 |
| rs778312568 | snp | A/C | 0.005231 | 0.0508737 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138073 | GCTTGACACTCTGAG[A/C]TGCCTGGATATCCAG | 377630 |
| rs778864778 | snp | A/G | 2.12651e-05 | 0.00326069 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137922 | TCGGAGAATCTCTTC[A/G]AGACAAGGATGAGGA | 377630 |
| rs778872965 | in-del | -/ACC | 3.14629e-05 | 0.00396616 | cds-indel, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137789 | CTCCACCCAGCGTGG[-/ACC]ACCAGCACAGCATAG | 377630 |
| rs778954861 | snp | C/T | 2.13879e-05 | 0.00327009 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137944 | GGATGAGGACCTTGG[C/T]AGAAGTGTGTAAAGT | 377630 |
| rs778956511 | snp | C/G/T | 3.68849e-05 | 0.00429434 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137462 | TTTCCAGTGGTCTAA[C/G/T]GTGCTTTCCTGAGTG | 377630 |
| rs778989922 | snp | C/T | 0.000169133 | 0.00919445 | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138790 | GGATCACAAGGTTTT[C/T]CTGCTGGGACTGCAG | 377630 |
| rs778990056 | snp | A/G | 4.53063e-05 | 0.00475932 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138357 | CCAGGACTGTGGAGG[A/G]CCCATGTGATGTGAG | 377630 |
| rs779079965 | snp | A/C | 6.47857e-05 | 0.0056911 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138404 | CATGCAGCACTTGGG[A/C]CGCTGACATGTTTGA | 377630 |
| rs779156667 | snp | C/G | 3.68997e-05 | 0.00429517 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137294 | CCGGGTCGTCGAAGA[C/G]AGGTTTAGCAGGGAG | 377630 |
| rs779341663 | snp | C/T | 2.911e-05 | 0.00381499 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137775 | TGTCCGTCGTGACAA[C/T]TCCACCCAGCGTGGA | 377630 |
| rs779428241 | snp | A/T | 1.84578e-05 | 0.00303786 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137360 | CTTGTATTTCGATTG[A/T]TGAATCACAAGTACG | 377630 |
| rs779447492 | snp | A/G | 5.18202e-05 | 0.00508993 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138042 | TCTTCGGGCTTCACC[A/G]ACTGTTCCAAAGCTT | 377630 |
| rs779466200 | snp | A/G | 2.54107e-05 | 0.00356437 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137989 | CCGGCGCCCTCTGGA[A/G]ACAAAGACCGCAATG | 377630 |
| rs779567213 | in-del | -/TA/TTTC | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12139172 | ATGAAACCGTGTGTG[-/TA/TTTC]TATCTCTCTGTGTGT | 377630 |
| rs779644781 | snp | A/G/T | 0.00113388 | 0.0237885 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137576 | GTCTGTGTCTTCAGC[A/G/T]CCGAGGGCTCTTGGT | 377630 |
| rs779719947 | snp | C/G | 1.84681e-05 | 0.0030387 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137148 | TCACCCCTACGTGTG[C/G]GTCGGCACTTCCACT | 377630 |
| rs779810100 | snp | A/C | 3.68915e-05 | 0.00429469 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137188 | GGCACACAAGCAGAG[A/C]CCTCTTGCTGTGTTT | 377630 |
| rs779827922 | snp | G/T | 2.67799e-05 | 0.00365913 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137869 | TGTCAAGGCACTCAG[G/T]ATATTGCACATTCTT | 377630 |
| rs780088271 | in-del | -/G | 1.84357e-05 | 0.00303604 | frameshift-variant, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137243 | CTCCCTTGCAGAGAA[-/G]GCGAGGGTGCCAGTG | 377630 |
| rs780100558 | snp | C/T | 4.25007e-05 | 0.00460962 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137917 | TGACATCGGAGAATC[C/T]CTTCAAGACAAGGAT | 377630 |
| rs780106944 | snp | A/C | 1.87749e-05 | 0.00306384 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138733 | TGAACTGCCACTCAC[A/C]TCCCAAGTAGAGTGA | 377630 |
| rs780196046 | snp | A/G | 8.98009e-05 | 0.00670018 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138350 | GACATGACCAGGACT[A/G]TGGAGGGCCCATGTG | 377630 |
| rs780567282 | snp | A/G | 1.78704e-05 | 0.00298913 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137693 | AGAAGTGATGCTACA[A/G]GCAGTGACCTTGGCA | 377630 |
| rs780671534 | snp | C/T | 3.66845e-05 | 0.00428263 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137730 | ATTTTATACCACTGG[C/T]CTTCTTGAGCTTTGA | 377630 |
| rs780689508 | snp | C/G | 2.14282e-05 | 0.00327317 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137958 | GCAGAAGTGTGTAAA[C/G]TTAACGTCTTGGAGG | 377630 |
| rs780779546 | snp | A/C | 4.90064e-05 | 0.00494983 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137981 | CTTGGAGGCCGGCGC[A/C]CTCTGGAGACAAAGA | 377630 |
| rs780942474 | snp | A/G/T | 0.000146971 | 0.00857121 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137527 | CCTGGAGGCAGGGGT[A/G/T]GTCTCTCTTGAGCTC | 377630 |
| rs780947817 | snp | A/G | 1.84735e-05 | 0.00303915 | downstream-variant-500B, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137143 | TGCGTTCACCCCTAC[A/G]TGTGGGTCGGCACTT | 377630 |
| rs780960345 | snp | C/T | 0.000377715 | 0.0137373 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138455 | GTAGTTGGCAAGGGG[C/T]GGTGTGTATGTCAGG | 377630 |
| rs781046117 | snp | C/G | 3.16771e-05 | 0.00397964 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137791 | TCCACCCAGCGTGGA[C/G]CAGCACAGCATAGAG | 377630 |
| rs781428963 | snp | C/G/T | 3.68862e-05 | 0.00429442 | stop-gained, missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137451 | TCTTGGGGGAATTTC[C/G/T]AGTGGTCTAAGGTGC | 377630 |
| rs781491001 | in-del | -/A | | | upstream-variant-2KB, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12140384 | AACAGCCCTGGCTTC[-/A]ATGGCCCATGAAATT | 377630 |
| rs781700530 | snp | A/G | 3.63062e-05 | 0.00426049 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12138299 | TTCCTGCTTGCCTCT[A/G]TGGAAGCCAGCAGCC | 377630 |
| rs781744008 | snp | A/G | 1.84446e-05 | 0.00303677 | synonymous-codon, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137204 | CCTCTTGCTGTGTTT[A/G]TTCTTCCCTTTGGAT | 377630 |
| rs781749796 | snp | A/G | 1.95242e-05 | 0.00312437 | missense, intron-variant | USP17L2, FAM66D | GRCh38.p7 | 8:12137652 | TTCTGGATGTAAAAG[A/G]GGACATAGGCCTGTT | 377630 |