| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs137952652 | snp | A/C | 0.286825 | 0.247273 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210398 | GTTCTGGAAGTCATG[A/C]TGTGGGCTGTGTCTG | 100287144 |
| rs139813323 | snp | C/T | 8.97304e-05 | 0.00669755 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210939 | TACGTGAACGCTTCC[C/T]TGCAGTGCCTGACAT | 100287144 |
| rs142481985 | snp | C/T | 0.0107246 | 0.0724382 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210496 | TTGGCTAATCGCGCA[C/T]CTGATGAGTGGGTGG | 100287144 |
| rs143756616 | snp | A/T | 0.191461 | 0.24305 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210259 | ACACACACGGTTTCC[A/T]AGGTAAAGATTTCTT | 100287144 |
| rs144060648 | snp | A/C | | | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212567 | ATTCAGTGTGTATTT[A/C]TGAATATGACCTACC | 100287144 |
| rs149415298 | snp | A/C | 0.411578 | 0.190768 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210229 | ACACACACAAACACA[A/C]TCACACACACACACA | 100287144 |
| rs149938208 | snp | C/T | | | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212548 | TGTGTTCATGATAGG[C/T]GACATTCAGTGTGTA | 100287144 |
| rs180979030 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209374 | CCCACTGAAACAAGG[A/G]CCAGTATTAAAAATG | 100287144 |
| rs181084641 | snp | C/T | 0.00304976 | 0.0389304 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210859 | CTCCCAGGGAGAAGC[C/T]TCCTCTGAGTAGCAG | 100287144 |
| rs181179919 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209334 | AGCGAGAATCCAGGA[G/T]ACACACGGCTTATTT | 100287144 |
| rs181304027 | snp | G/T | | | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212688 | ACGAGAAGGTGAAAT[G/T]TGGCTCATGTGGGAC | 100287144 |
| rs181412811 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9208858 | TGCTTTCTCCCTGTG[G/T]AGCATCTTTCTAAGC | 100287144 |
| rs181632685 | snp | A/G | 0.00478085 | 0.0486577 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212418 | CAAGTTTCTGTCTGT[A/G]CAACAGGGACAACTG | 100287144 |
| rs181643214 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9208800 | AAGCCACGGCATCTG[C/G]ATTGCTCATGCTTCT | 100287144 |
| rs181820493 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9208908 | AGGAAACTTTACATC[A/C]GGCACAGGAAGCTTT | 100287144 |
| rs181833188 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209937 | AACACTTGTCTTGTT[C/G]TCCACTGGCAAGTAA | 100287144 |
| rs181950327 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209438 | AACGTCTCCGATGTT[G/T]CTTCTTGAGACAGGG | 100287144 |
| rs182083040 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209964 | GTAATTCAACACGGA[C/T]AGAGAATCAATAGGC | 100287144 |
| rs182169107 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210540 | GGTGTGGGTGAGTTA[C/T]AGAAGGGCTGATGCG | 100287144 |
| rs182339908 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209512 | GTTTGCTTTTGTCAA[A/C]CTTAGAACATTTTAT | 100287144 |
| rs182541833 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210069 | ACGCTGTGCTAAATA[C/T]TATACTTCATTGACT | 100287144 |
| rs182607432 | snp | C/G | 0.000697107 | 0.0186566 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212030 | AAGAGTCGAAGGTAC[C/G]GTGCCTCCCGACGTA | 100287144 |
| rs182819472 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209453 | TCTTCTTGAGACAGG[A/G]CCTCACTGCCGTCCG | 100287144 |
| rs183042461 | snp | C/T | 0.0010771 | 0.0231817 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210985 | CCAACTACATGCTGT[C/T]CCGGGAGCACTCTCA | 100287144 |
| rs183192822 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9208994 | TCACACTCCTCTCAT[C/T]CCATCATACTCCTTA | 100287144 |
| rs183285001 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209024 | AAAATCATCCTAATT[C/T]CATGGGTCCTGAAGC | 100287144 |
| rs183368930 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209621 | TATTTTCATCACTTC[A/C]AGAAAAAAAAGGGTA | 100287144 |
| rs183631483 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209884 | CATATGATGCTTTAT[C/T]ATTTGGCAATCTAGC | 100287144 |
| rs183806930 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210103 | CTCAGGTCAGAAAGC[A/G]CACTTCCGAATTCTT | 100287144 |
| rs183818171 | snp | A/G | 0.0197687 | 0.0974348 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210130 | TCTTGTCCTTCGGTC[A/G]CTGAGAGGATGATGG | 100287144 |
| rs183887405 | snp | A/G | 0.00140305 | 0.0264492 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211174 | CTGTGGATGCCATGA[A/G]AAAGGCATGCCTTCC | 100287144 |
| rs183981664 | snp | A/T | | | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212439 | GGGACAACTGGATAG[A/T]GATGGCTACATCTCA | 100287144 |
| rs183983725 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9208826 | CTTCTGGGGATCATT[C/T]TCCTGAAAATCGTGG | 100287144 |
| rs184205409 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209197 | ATTCTGTCCCTCTTA[A/C]TTCAGGGAACGTGTC | 100287144 |
| rs184255491 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210378 | AGGAGTAATCTGATT[C/G]AGGTGTTCTGGAAGT | 100287144 |
| rs184637313 | snp | A/C/G | 0.00631449 | 0.0558334 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212190 | TCCCTACGAGGGAGG[A/C/G]CCAGGAGATCCAAAG | 100287144 |
| rs184639008 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209129 | TGTTGGGAAAGTCCC[A/T]AGAGCCAGGATCTTC | 100287144 |
| rs184665396 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209825 | TCCTACACAGTCTAC[A/T]TTGTGCACTGAGTAT | 100287144 |
| rs184768925 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9208713 | GCTCCCCTCAAAAGC[G/T]GTTATGAGCATTAAA | 100287144 |
| rs184946946 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209336 | CGAGAATCCAGGAGA[A/C]ACACGGCTTATTTTG | 100287144 |
| rs184981556 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210095 | TGACTATTCTCAGGT[A/C]AGAAAGCACACTTCC | 100287144 |
| rs185462842 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210529 | TGTTCGCGGTTGGTG[G/T]GGGTGAGTTATAGAA | 100287144 |
| rs185609693 | snp | A/C | 0.000536241 | 0.0163656 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210958 | AGTGCCTGACATACA[A/C]ACCGCCACTTGCCAA | 100287144 |
| rs185624630 | snp | A/G | | | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212412 | GGAGCCCAAGTTTCT[A/G]TCTGTACAACAGGGA | 100287144 |
| rs185777226 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9208881 | TTCTAAGCAGTGCTC[C/T]TTTCTTCCCACAGGA | 100287144 |
| rs186330055 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210056 | TAGGGAAGAAAATAC[A/G]CTGTGCTAAATATTA | 100287144 |
| rs186426447 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209391 | CAGTATTAAAAATGG[C/T]ATGCTATACTCTGTT | 100287144 |
| rs186545087 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209441 | GTCTCCGATGTTTCT[C/T]CTTGAGACAGGGCCT | 100287144 |
| rs186548755 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9208921 | TCAGGCACAGGAAGC[C/T]TTCTGATGGAGCACA | 100287144 |
| rs186691912 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209538 | TTTATTTCGTCTCTA[G/T]GAAATGTTGATCCAT | 100287144 |
| rs186786338 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210566 | ATGCGGCCAGAGAGC[C/T]CGTCATTTGAAGACT | 100287144 |
| rs187120998 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209002 | CTCTCATTCCATCAT[A/C]CTCCTTAAAATCATC | 100287144 |
| rs187156447 | snp | A/T | 0.000470655 | 0.0153332 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211069 | CAAGGGCCCTCCACA[A/T]TCCTGGCCATGTCAT | 100287144 |
| rs187262693 | snp | C/G/T | 0.0312266 | 0.12106 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212076 | TCAAAATACAAGTGT[C/G/T]GGATGAAGAACCATC | 100287144 |
| rs187420227 | snp | C/T | 0.00575911 | 0.0533516 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211663 | ACAACGGACATTACT[C/T]CTCTTATGTCAAAGC | 100287144 |
| rs187455159 | snp | A/G | 0.00795532 | 0.062565 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209948 | TGTTGTCCACTGGCA[A/G]GTAATTCAACACGGA | 100287144 |
| rs187500889 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209031 | TCCTAATTTCATGGG[C/T]CCTGAAGCCAGGGCT | 100287144 |
| rs187608883 | snp | A/C | 0.00517822 | 0.0506191 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212192 | CCTACGAGGGAGGAC[A/C]AGGAGATCCAAAGGG | 100287144 |
| rs187857232 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209152 | GGATCTTCATTCCTG[C/G]TAAGGCAGACAGAAT | 100287144 |
| rs188143133 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210405 | AAGTCATGATGTGGG[A/C]TGTGTCTGTTGAATT | 100287144 |
| rs188241677 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209660 | ATACCTTCTGATTTC[A/T]CAAGATTTTTCTTTC | 100287144 |
| rs188297990 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209924 | AGCATTTCATGCAAA[C/G]ACTTGTCTTGTTGTC | 100287144 |
| rs188392761 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209461 | AGACAGGGCCTCACT[G/T]CCGTCCGCCGGGCTA | 100287144 |
| rs188408246 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210202 | AACACACATACACAC[A/G]CGCCCCCCCCCACAC | 100287144 |
| rs188713313 | snp | C/T | | | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212674 | AGTTGTTGGTCGGCA[C/T]GAGAAGGTGAAATTT | 100287144 |
| rs188798303 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9208790 | ACCCTGTGGGAAGCC[A/T]CGGCATCTGGATTGC | 100287144 |
| rs188888630 | snp | C/G | 0.0322114 | 0.122752 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212416 | CCCAAGTTTCTGTCT[C/G]TACAACAGGGACAAC | 100287144 |
| rs189033959 | snp | A/G/T | 0.00349783 | 0.0416793 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210757 | TTGCTGAAATCCAGC[A/G/T]TACTTCTCTCCCTGA | 100287144 |
| rs189115338 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209373 | TCCCACTGAAACAAG[A/G]ACCAGTATTAAAAAT | 100287144 |
| rs189174316 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210109 | TCAGAAAGCACACTT[C/T]CGAATTCTTGTCCTT | 100287144 |
| rs189629846 | snp | A/C | 0.000357814 | 0.0133708 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210965 | GACATACAAACCGCC[A/C]CTTGCCAACTACATG | 100287144 |
| rs189762637 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9208844 | CTGAAAATCGTGGCT[C/G]CTTTCTCCCTGTGTA | 100287144 |
| rs189775958 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210101 | TTCTCAGGTCAGAAA[A/G]CACACTTCCGAATTC | 100287144 |
| rs189915097 | snp | A/T | 0.00795532 | 0.062565 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209959 | GGCAAGTAATTCAAC[A/T]CGGATAGAGAATCAA | 100287144 |
| rs189956136 | snp | A/G | 0.00597247 | 0.0543191 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210068 | TACGCTGTGCTAAAT[A/G]TTATACTTCATTGAC | 100287144 |
| rs190035450 | snp | C/G | 0.0174175 | 0.0916809 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209861 | CAAACTTCAGTGCTT[C/G]TTTCTACCATATGAT | 100287144 |
| rs190263201 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209257 | CAAATGTGCTAACTG[C/G]AATTCCACCATACAA | 100287144 |
| rs190554546 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9208984 | GGGCCAAAGGTCACA[C/G]TCCTCTCATTCCATC | 100287144 |
| rs190685821 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209467 | GGCCTCACTGCCGTC[A/C]GCCGGGCTATCTAGA | 100287144 |
| rs190696563 | snp | C/T | 0.0124255 | 0.0778353 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211843 | CAAGAGCCCTTGGCG[C/T]AGAAGACACAGACAG | 100287144 |
| rs190813900 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210536 | GGTTGGTGTGGGTGA[C/G]TTATAGAAGGGCTGA | 100287144 |
| rs191017496 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209005 | TCATTCCATCATACT[A/C]CTTAAAATCATCCTA | 100287144 |
| rs191118388 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9208888 | CAGTGCTCCTTTCTT[C/G]CCACAGGAAACTTTA | 100287144 |
| rs191192619 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209393 | GTATTAAAAATGGTA[C/T]GCTATACTCTGTTTC | 100287144 |
| rs191387875 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209872 | GCTTCTTTCTACCAT[A/T]TGATGCTTTATCATT | 100287144 |
| rs191405498 | snp | A/G | | | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212164 | AGTCCATGAACACTG[A/G]CACACTCGCTTCCCT | 100287144 |
| rs191550242 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210487 | GATATTTGATTGGCT[A/T]ATCGCGCACCTGATG | 100287144 |
| rs191624460 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210246 | CACACACACACACAC[A/T]CACACGGTTTCCAAG | 100287144 |
| rs191956788 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209443 | CTCCGATGTTTCTTC[C/T]TGAGACAGGGCCTCA | 100287144 |
| rs192066609 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209179 | GAATGAAGACACACC[A/C]AAATTCTGTCCCTCT | 100287144 |
| rs192119522 | snp | C/T | 0.000191957 | 0.00979498 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211079 | CCACATTCCTGGCCA[C/T]GTCATCCAGCCCTCA | 100287144 |
| rs192321728 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209543 | TTCGTCTCTATGAAA[C/T]GTTGATCCATTATCA | 100287144 |
| rs192740929 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209124 | AGACATGTTGGGAAA[A/G]TCCCAAGAGCCAGGA | 100287144 |
| rs192898468 | snp | A/C | 0.0146672 | 0.084371 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210113 | AAAGCACACTTCCGA[A/C]TTCTTGTCCTTCGGT | 100287144 |
| rs193189159 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209788 | TCAAATAGTCTCCCG[A/C]TGATTGCATGATTCC | 100287144 |
| rs193227739 | snp | G/T | | | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212283 | CCCACACGTAGGGGT[G/T]CATACACACACACAC | 100287144 |
| rs200096337 | in-del | -/ACAT | | | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212313 | CACACACACACACAC[-/ACAT]AACTACACCCAGAAG | 100287144 |
| rs200661664 | in-del | -/TT | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9208900 | CTTCCCACAGGAAAC[-/TT]TACATCAGGCACAGG | 100287144 |
| rs201780477 | in-del | -/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210352 | TCCTATTATATGTGC[-/T]TATCATCCTGAGGAG | 100287144 |
| rs367633941 | snp | A/G | | | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212740 | CCTTGAATAGTGGAA[A/G]CTGGAATGCATTTGG | 100287144 |
| rs367640585 | snp | A/G | | | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211004 | GGAGCACTCTCAAAC[A/G]TGTCATCGTCACAAG | 100287144 |
| rs367849853 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210466 | CTCCTTCCTGAATTG[A/G]GTGCTGATATTTGAT | 100287144 |
| rs367901084 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210195 | CAGCACAAACACACA[C/T]ACACACACGCCCCCC | 100287144 |
| rs367950303 | snp | A/C/T | 0.031488 | 0.12146 | stop-gained, synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211898 | GAGAGACCACCCCTG[A/C/T]CTCCAGGCCCCCGAG | 100287144 |
| rs368728155 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209276 | TCCACCATACAATGC[A/C]TAACTGGAAATGGAG | 100287144 |
| rs368919398 | snp | A/C | 0.00439282 | 0.0466596 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211468 | CGTTAACTTTACACA[A/C]CTCTGCCAAGGTCCT | 100287144 |
| rs368958246 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209431 | GCTTTTAAACGTCTC[C/T]GATGTTTCTTCTTGA | 100287144 |
| rs368968666 | snp | C/G | | | stop-gained, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210677 | GGACGACTCACTCTA[C/G]TTGGGAGGTGAGTGG | 100287144 |
| rs369564189 | snp | A/G | 0.430136 | 0.173352 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210592 | AGACTCTCTCGGAAG[A/G]GATAGCGTCTTTCTG | 100287144 |
| rs369753918 | snp | C/T | | | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211150 | ATGCCCATGAATTTC[C/T]CATGTTCACTGTGGA | 100287144 |
| rs370452127 | snp | A/T | | | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212657 | GGTGTGTTTCATTCG[A/T]CAGTTGTTGGTCGGC | 100287144 |
| rs370533531 | snp | G/T | 0.0038146 | 0.0435057 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210758 | TGCTGAAATCCAGCG[G/T]ACTTCTCTCCCTGAG | 100287144 |
| rs370795411 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210311 | AATAAGGCAACTGTG[A/T]GGCCACTGTCCCAAC | 100287144 |
| rs370796842 | snp | G/T | 0.00331916 | 0.0406025 | stop-gained, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210852 | CAGCTTGCTCCCAGG[G/T]AGAAGCCTCCTCTGA | 100287144 |
| rs370962470 | snp | C/T | | | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212537 | GTCTGAGTGTTTGTG[C/T]TCATGATAGGTGACA | 100287144 |
| rs371241066 | snp | A/C/G | 0.00106085 | 0.023008 | missense, synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211526 | TGTCACAGGCAACAA[A/C/G]ATTGCCAAGAATGTG | 100287144 |
| rs371252430 | snp | A/G | 0.000603682 | 0.0173631 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211845 | AGAGCCCTTGGCGTA[A/G]AAGACACAGACAGGC | 100287144 |
| rs371373089 | snp | G/T | | | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211725 | GCCGAGGTCACCGCC[G/T]CTAGCATCACTTCTG | 100287144 |
| rs371466590 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210479 | TGAGTGCTGATATTT[C/G]ATTGGCTAATCGCGC | 100287144 |
| rs371580025 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210040 | ATCTCTCCTTTCTCA[C/T]TAGGGAAGAAAATAC | 100287144 |
| rs371876142 | snp | A/T | 8.43206e-05 | 0.00649255 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211100 | CCAGCCCTCACAGGC[A/T]TTGGCTGCTGGCTTC | 100287144 |
| rs372240080 | snp | A/C | 0.000185667 | 0.00963321 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211056 | CAAGCTCACATCACA[A/C]GGGCCCTCCACATTC | 100287144 |
| rs372354972 | snp | C/G | 0.00542524 | 0.0517995 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212142 | TCGACGACCCCGACA[C/G]ATCAGGAGTCCATGA | 100287144 |
| rs372424646 | snp | A/C | 0.00226167 | 0.0335518 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210731 | CACATCTTCTCGGCC[A/C]GATGCAGCTTTTGCT | 100287144 |
| rs372491968 | snp | C/G/T | 0.00199481 | 0.0315187 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212340 | CCAGAAGCGCGCACG[C/G/T]AAACACACACACACC | 100287144 |
| rs373485739 | snp | C/T | | | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211481 | CAACTCTGCCAAGGT[C/T]CTCATCCTTGTATTG | 100287144 |
| rs373979712 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9208797 | GGGAAGCCACGGCAT[C/G]TGGATTGCTCATGCT | 100287144 |
| rs374023730 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210171 | AAGTACATACTTGGA[A/G]GTTCATCCCAGCACA | 100287144 |
| rs374024924 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209978 | ATAGAGAATCAATAG[A/G]CTCAACGTGGAAAGG | 100287144 |
| rs374087491 | snp | A/C | 0.000868961 | 0.0208261 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210625 | ACCTGCGGTCCCAGC[A/C]GAAAAACCTTGTGAT | 100287144 |
| rs374192488 | snp | C/T | 0.00222579 | 0.0332858 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211601 | GAACACAGGACCTCT[C/T]GTCTATGTCCTCTAT | 100287144 |
| rs374796104 | snp | A/C | | | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211869 | GACAGGCGAGCAACG[A/C]AAGGAGAGCTCAAGA | 100287144 |
| rs375076086 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210316 | GGCAACTGTGTGGCC[A/G]CTGTCCCAACCCGGT | 100287144 |
| rs375228799 | snp | C/G | 0.00069533 | 0.0186328 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212031 | AGAGTCGAAGGTACG[C/G]TGCCTCCCGACGTAC | 100287144 |
| rs375415915 | snp | A/C/G | 0.00747595 | 0.0607236 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212180 | CACACTCGCTTCCCT[A/C/G]CGAGGGAGGACCAGG | 100287144 |
| rs375781055 | snp | A/G | 0.000901771 | 0.0212149 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211210 | ACAAGCAGGTAGATC[A/G]TCACTCTAAGGACAC | 100287144 |
| rs375833666 | snp | A/C | 0.357451 | 0.225731 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210432 | AATTCCCAGCGATGC[A/C]AGGGGACACACCCTG | 100287144 |
| rs375927397 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209399 | AAAATGGTATGCTAT[A/C]CTCTGTTTCACTCCC | 100287144 |
| rs376073603 | snp | A/G | | | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211804 | GGGAAAGACACAGTG[A/G]GAGTGTGTCAAGAGG | 100287144 |
| rs376358740 | snp | C/T | 9.32271e-05 | 0.00682677 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211506 | GTATTGAAGAGATTC[C/T]CCGATGTCACAGGCA | 100287144 |
| rs376769490 | snp | C/T | | | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211113 | GCATTGGCTGCTGGC[C/T]TCCATAGAGGCAAGC | 100287144 |
| rs376857483 | snp | C/T | 0.00455994 | 0.0475308 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210644 | AAACCTTGTGATCCT[C/T]GTTCCAGTCGACATG | 100287144 |
| rs377006210 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210015 | CTGGAAGGTCTGTTT[A/G]ATTCCACGGATCTCT | 100287144 |
| rs377406489 | snp | C/T | | | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210842 | TGTGGCAAGACAGCT[C/T]GCTCCCAGGGAGAAG | 100287144 |
| rs377677903 | snp | A/T | | | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212515 | CTTCCGAACCTCTGG[A/T]GGGACTGTCTGAGTG | 100287144 |
| rs528229407 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210212 | CACACACGCCCCCCC[A/C]CACACACACAAACAC | 100287144 |
| rs528291442 | snp | A/G | 0.0412342 | 0.137538 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210950 | TTCCCTGCAGTGCCT[A/G]ACATACAAACCGCCA | 100287144 |
| rs528401515 | snp | C/T | 0.0221141 | 0.102801 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210422 | GTGTCTGTTGAATTC[C/T]CAGCGATGCAAGGGG | 100287144 |
| rs529142859 | in-del | -/A | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210206 | ACATACACACACGCC[-/A]CCCCCCCACACACAC | 100287144 |
| rs529560351 | snp | A/C | 0.000839379 | 0.0204691 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212125 | CCCTGCTAAACCTCT[A/C]TTCGACGACCCCGAC | 100287144 |
| rs529798765 | snp | A/C | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209882 | ACCATATGATGCTTT[A/C]TCATTTGGCAATCTA | 100287144 |
| rs530075390 | snp | C/G | 0.0150606 | 0.0854603 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210443 | ATGCAAGGGGACACA[C/G]CCTGTGACTCCTTCC | 100287144 |
| rs530078335 | snp | A/G | 0.000400882 | 0.014152 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210747 | GATGCAGCTTTTGCT[A/G]AAATCCAGCGTACTT | 100287144 |
| rs530649941 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209946 | CTTGTTGTCCACTGG[A/C]AAGTAATTCAACACG | 100287144 |
| rs530847012 | snp | A/C | 0.000909008 | 0.0212997 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211585 | CATACATGTCTCAGC[A/C]GAACACAGGACCTCT | 100287144 |
| rs530909346 | snp | C/G | 0.000399281 | 0.0141238 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210781 | TCCCTGAGAAGTCAC[C/G]ACTCTCATGTGAGAC | 100287144 |
| rs532511737 | snp | C/T | 0.00795532 | 0.062565 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209955 | CACTGGCAAGTAATT[C/T]AACACGGATAGAGAA | 100287144 |
| rs534274272 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210207 | ACATACACACACGCC[C/G]CCCCCCACACACACA | 100287144 |
| rs534975967 | snp | A/G | 0.0142736 | 0.0832652 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210532 | TCGCGGTTGGTGTGG[A/G]TGAGTTATAGAAGGG | 100287144 |
| rs535386666 | snp | C/T | 0.0229021 | 0.10453 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210961 | GCCTGACATACAAAC[C/T]GCCACTTGCCAACTA | 100287144 |
| rs536324943 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210241 | ACACTCACACACACA[A/C]ACACACACACGGTTT | 100287144 |
| rs537214825 | snp | A/G | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210491 | TTTGATTGGCTAATC[A/G]CGCACCTGATGAGTG | 100287144 |
| rs537276298 | snp | C/G | 0.0197687 | 0.0974348 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210126 | GAATTCTTGTCCTTC[C/G]GTCACTGAGAGGATG | 100287144 |
| rs537791058 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210287 | CTTCCCTGCCATTGC[A/T]TTACCTAAAATAAGG | 100287144 |
| rs539532579 | snp | A/C | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211190 | AAAGGCATGCCTTCC[A/C]GGGCACAAGCAGGTA | 100287144 |
| rs540647749 | snp | C/T | 0.0174175 | 0.0916809 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209860 | TCAAACTTCAGTGCT[C/T]CTTTCTACCATATGA | 100287144 |
| rs541133109 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209452 | TTCTTCTTGAGACAG[A/G]GCCTCACTGCCGTCC | 100287144 |
| rs541544568 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210537 | GTTGGTGTGGGTGAG[C/T]TATAGAAGGGCTGAT | 100287144 |
| rs543698468 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209812 | TGATTCCACAAAGTC[C/T]TACACAGTCTACATT | 100287144 |
| rs544541840 | snp | C/T | 0.00945174 | 0.0680921 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211574 | TGACATGCAGCCATA[C/T]ATGTCTCAGCAGAAC | 100287144 |
| rs545976781 | snp | G/T | 0.000399281 | 0.0141238 | stop-gained, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210687 | CTCTACTTGGGAGGT[G/T]AGTGGCAGTTCAACC | 100287144 |
| rs546034102 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210358 | TATATGTGCTTATCA[C/T]CCTGAGGAGTAATCT | 100287144 |
| rs546799537 | snp | A/G | 0.000718197 | 0.0189363 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210988 | ACTACATGCTGTTCC[A/G]GGAGCACTCTCAAAC | 100287144 |
| rs546885725 | snp | C/G/T | 0.00243988 | 0.0348481 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212111 | TGAACAGCAAAGCTC[C/G/T]CTGCTAAACCTCTCT | 100287144 |
| rs547589005 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210214 | CACACGCCCCCCCCC[A/C]CACACACAAACACAC | 100287144 |
| rs547824145 | snp | A/C | 0.00795532 | 0.062565 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209956 | ACTGGCAAGTAATTC[A/C]ACACGGATAGAGAAT | 100287144 |
| rs548392613 | snp | A/G | 0.00020749 | 0.0101834 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211541 | AATTGCCAAGAATGT[A/G]CAATATCCTGAGTGC | 100287144 |
| rs548643547 | snp | C/T | 0.0267878 | 0.112589 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210452 | GACACACCCTGTGAC[C/T]CCTTCCTGAATTGAG | 100287144 |
| rs552292284 | snp | A/C/T | 0.000467854 | 0.0152884 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210807 | GAGACCCGTGTCGAC[A/C/T]TCTGTGATGATTTGG | 100287144 |
| rs553422908 | snp | A/C | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210551 | GTTATAGAAGGGCTG[A/C]TGCGGCCAGAGAGCT | 100287144 |
| rs556688086 | snp | G/T | 0.000717039 | 0.018921 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210982 | TTGCCAACTACATGC[G/T]GTTCCGGGAGCACTC | 100287144 |
| rs556981603 | snp | A/C | 0.000890868 | 0.0210865 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210628 | TGCGGTCCCAGCAGA[A/C]AAACCTTGTGATCCT | 100287144 |
| rs557859120 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212258 | CCAGTGATCTCAGTG[C/G]AAGTACCGACCCACA | 100287144 |
| rs557923842 | snp | G/T | 0.00372438 | 0.0429921 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211352 | CCAGGCAGCTCAGAG[G/T]GTCCAGCAAGCTTTG | 100287144 |
| rs558858295 | snp | A/T | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209814 | ATTCCACAAAGTCCT[A/T]CACAGTCTACATTGT | 100287144 |
| rs559239144 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209128 | ATGTTGGGAAAGTCC[C/T]AAGAGCCAGGATCTT | 100287144 |
| rs559691645 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210434 | TTCCCAGCGATGCAA[C/G]GGGACACACCCTGTG | 100287144 |
| rs561864149 | snp | A/G/T | 0.000798403 | 0.0199641 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210738 | TCTCGGCCAGATGCA[A/G/T]CTTTTGCTGAAATCC | 100287144 |
| rs563265920 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210280 | AAGATTTCTTCCCTG[A/C]CATTGCTTTACCTAA | 100287144 |
| rs563333777 | snp | A/T | 0.000499127 | 0.0157897 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211576 | ACATGCAGCCATACA[A/T]GTCTCAGCAGAACAC | 100287144 |
| rs563488185 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209944 | GTCTTGTTGTCCACT[A/G]GCAAGTAATTCAACA | 100287144 |
| rs564004270 | snp | A/C | 0.00018031 | 0.00949329 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210902 | GGTGGGGGCTGGGCT[A/C]CAGAATATGGGAAAT | 100287144 |
| rs564260471 | snp | C/T | 0.00165792 | 0.0287439 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211993 | AAGAGCAAAACAAAA[C/T]GAAGCCTGAGTTCAA | 100287144 |
| rs564274009 | snp | A/T | 0.00446426 | 0.0470341 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210705 | TGGCAGTTCAACCAC[A/T]TTTCAAAACTCACAT | 100287144 |
| rs564390930 | snp | A/C | 0.00795532 | 0.062565 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209952 | GTCCACTGGCAAGTA[A/C]TTCAACACGGATAGA | 100287144 |
| rs566587205 | snp | C/T | 0.395818 | 0.203069 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212286 | ACACGTAGGGGTGCA[C/T]ACACACACACACACA | 100287144 |
| rs568687855 | snp | A/T | 0.00119737 | 0.0244387 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212116 | AGCAAAGCTCCCTGC[A/T]AAACCTCTCTTCGAC | 100287144 |
| rs568857895 | snp | C/G | 0.00180976 | 0.0300267 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212172 | AACACTGGCACACTC[C/G]CTTCCCTACGAGGGA | 100287144 |
| rs568922052 | snp | A/C | 0.0182793 | 0.0938377 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211077 | CTCCACATTCCTGGC[A/C]ATGTCATCCAGCCCT | 100287144 |
| rs569542114 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9208714 | CTCCCCTCAAAAGCT[A/G]TTATGAGCATTAAAG | 100287144 |
| rs569943501 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210284 | TTTCTTCCCTGCCAT[G/T]GCTTTACCTAAAATA | 100287144 |
| rs570695354 | snp | C/T | 0.00121706 | 0.0246383 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210815 | TGTCGACCTCTGTGA[C/T]GATTTGGCTCCTGTG | 100287144 |
| rs570757040 | snp | A/T | 0.0170251 | 0.090679 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210501 | TAATCGCGCACCTGA[A/T]GAGTGGGTGGGGTGT | 100287144 |
| rs573053803 | snp | A/C/G | 0.000280348 | 0.0118362 | synonymous-codon, missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211451 | GGCGCCGGCCTCCAA[A/C/G]ACGTTAACTTTACAC | 100287144 |
| rs573117972 | snp | C/T | 0.0460142 | 0.144533 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210723 | TCAAAACTCACATCT[C/T]CTCGGCCAGATGCAG | 100287144 |
| rs573862364 | snp | A/C | 0.00279162 | 0.0372561 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211527 | GTCACAGGCAACAAA[A/C]TTGCCAAGAATGTGC | 100287144 |
| rs574351048 | snp | A/T | 0.0111196 | 0.0737302 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210552 | TTATAGAAGGGCTGA[A/T]GCGGCCAGAGAGCTC | 100287144 |
| rs574390306 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210233 | ACACAAACACACTCA[C/G]ACACACACACACACA | 100287144 |
| rs575479907 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210281 | AGATTTCTTCCCTGC[A/C]ATTGCTTTACCTAAA | 100287144 |
| rs576408470 | snp | A/T | 0.0174175 | 0.0916809 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209859 | TTCAAACTTCAGTGC[A/T]TCTTTCTACCATATG | 100287144 |
| rs576609175 | snp | G/T | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209810 | CATGATTCCACAAAG[G/T]CCTACACAGTCTACA | 100287144 |
| rs577128134 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210155 | TGATGGTAGCTGCCA[A/G]AAGTACATACTTGGA | 100287144 |
| rs577512473 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9209137 | AAGTCCCAAGAGCCA[C/G]GATCTTCATTCCTGG | 100287144 |
| rs745594359 | snp | A/G | 0.000667557 | 0.0182574 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211840 | AACCAAGAGCCCTTG[A/G]CGTAGAAGACACAGA | 100287144 |
| rs745640674 | snp | G/T | 0.000182548 | 0.00955201 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211037 | CTGCATGCTCTGTAC[G/T]ATGCAAGCTCACATC | 100287144 |
| rs745871685 | snp | G/T | 0.00021561 | 0.0103807 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211146 | GAAGATGCCCATGAA[G/T]TTCTCATGTTCACTG | 100287144 |
| rs746004323 | in-del | -/T | | | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212286 | ACACGTAGGGGTGCA[-/T]ACACACACACACACA | 100287144 |
| rs746082622 | in-del | -/G | 0.00013421 | 0.00819067 | frameshift-variant, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210855 | TTGCTCCCAGGGAGA[-/G]AGCCTCCTCTGAGTA | 100287144 |
| rs746186134 | snp | A/G | 0.00031294 | 0.0125049 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212299 | CATACACACACACAC[A/G]CACACACACACACAC | 100287144 |
| rs746318051 | snp | A/G | 0.000491159 | 0.0156633 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211602 | AACACAGGACCTCTC[A/G]TCTATGTCCTCTATG | 100287144 |
| rs746419300 | snp | A/C | 0.000186168 | 0.0096462 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211505 | TGTATTGAAGAGATT[A/C]CCCGATGTCACAGGC | 100287144 |
| rs746551326 | snp | A/G | 0.000205086 | 0.0101243 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211107 | TCACAGGCATTGGCT[A/G]CTGGCTTCCATAGAG | 100287144 |
| rs746792151 | snp | A/G/T | 0.000505913 | 0.0158981 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212000 | AAACAAAACGAAGCC[A/G/T]GAGTTCAACGTCAGA | 100287144 |
| rs746841954 | snp | A/T | | | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211513 | AGAGATTCCCCGATG[A/T]CACAGGCAACAAAAT | 100287144 |
| rs746856780 | snp | C/T | 0.000360653 | 0.0134237 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211005 | GAGCACTCTCAAACG[C/T]GTCATCGTCACAAGG | 100287144 |
| rs747027961 | snp | A/T | 0.000178891 | 0.00945587 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210949 | CTTCCCTGCAGTGCC[A/T]GACATACAAACCGCC | 100287144 |
| rs747065702 | snp | C/T | 0.000381025 | 0.0137974 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211490 | CAAGGTCCTCATCCT[C/T]GTATTGAAGAGATTC | 100287144 |
| rs747263166 | in-del | -/AC/ACAC | 0.149683 | 0.233131 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212286 | CACGTAGGGGTGCAT[-/AC/ACAC]ACACACACACACACA | 100287144 |
| rs747302822 | snp | A/C | 0.000177952 | 0.00943102 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211584 | CCATACATGTCTCAG[A/C]AGAACACAGGACCTC | 100287144 |
| rs747355639 | snp | A/C | 9.39011e-05 | 0.0068514 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210803 | ATGTGAGACCCGTGT[A/C]GACCTCTGTGATGAT | 100287144 |
| rs747480442 | snp | C/G | 0.000105725 | 0.00726989 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212296 | GTGCATACACACACA[C/G]ACACACACACACACA | 100287144 |
| rs747531869 | snp | A/C/G | 0.000296291 | 0.0121685 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212268 | CAGTGGAAGTACCGA[A/C/G]CCACACGTAGGGGTG | 100287144 |
| rs747643973 | snp | A/G | 0.000358295 | 0.0133798 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210941 | CGTGAACGCTTCCCT[A/G]CAGTGCCTGACATAC | 100287144 |
| rs747966480 | snp | C/T | 0.00102496 | 0.0226149 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211988 | CCTTCAAGAGCAAAA[C/T]AAAACGAAGCCTGAG | 100287144 |
| rs748151197 | snp | C/T | 0.000306607 | 0.0123778 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211899 | AGAGACCACCCCTGC[C/T]TCCAGGCCCCCGAGT | 100287144 |
| rs748210343 | snp | A/C/T | 0.000495103 | 0.0157274 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212265 | TCTCAGTGGAAGTAC[A/C/T]GACCCACACGTAGGG | 100287144 |
| rs748337722 | snp | A/T | 0.000189268 | 0.00972617 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211486 | CTGCCAAGGTCCTCA[A/T]CCTTGTATTGAAGAG | 100287144 |
| rs748381437 | snp | A/G | 0.000958773 | 0.0218739 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211344 | CTGGATATCCAGGCA[A/G]CTCAGAGTGTCCAGC | 100287144 |
| rs748443196 | snp | A/C | 7.88364e-05 | 0.0062779 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212292 | AGGGGTGCATACACA[A/C]ACACACACACACACA | 100287144 |
| rs748493500 | snp | A/C | 0.0032613 | 0.0402494 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211828 | CAAGAGGCAGGGAAC[A/C]AAGAGCCCTTGGCGT | 100287144 |
| rs748722593 | snp | C/G | 8.24029e-05 | 0.00641831 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210702 | GAGTGGCAGTTCAAC[C/G]ACTTTTCAAAACTCA | 100287144 |
| rs748784633 | snp | G/T | 0.00121359 | 0.0246033 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211897 | AGAGAGACCACCCCT[G/T]CCTCCAGGCCCCCGA | 100287144 |
| rs748831217 | snp | A/C/T | 0.000269054 | 0.011596 | synonymous-codon, missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210932 | TACCTGCTACGTGAA[A/C/T]GCTTCCCTGCAGTGC | 100287144 |
| rs749011703 | snp | G/T | 0.000569152 | 0.0168598 | stop-gained, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211957 | CTCAGGAAAGCACCT[G/T]AGACCACTGGAAATT | 100287144 |
| rs749099508 | snp | A/C | 0.00018577 | 0.0096359 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211289 | GTGTCTCCACTGCCA[A/C]GGCATTTCAGACACT | 100287144 |
| rs749353530 | snp | A/G | 0.000176663 | 0.00939682 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210682 | ACTCACTCTACTTGG[A/G]AGGTGAGTGGCAGTT | 100287144 |
| rs749442485 | snp | A/G | 0.000538242 | 0.0163961 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211167 | ATGTTCACTGTGGAT[A/G]CCATGAGAAAGGCAT | 100287144 |
| rs749590748 | snp | G/T | 0.000758054 | 0.0194539 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211621 | ATGTCCTCTATGCTG[G/T]GCTGGTCCACGCTGG | 100287144 |
| rs749765613 | in-del | -/CATA | 0.000104756 | 0.0072365 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212284 | CCACACGTAGGGGTG[-/CATA]CACACACACACACAC | 100287144 |
| rs749870602 | snp | C/G | 0.000294507 | 0.0121312 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211678 | CCTCTTATGTCAAAG[C/G]TCAAGAAGGCCAGTG | 100287144 |
| rs749939100 | in-del | -/C | | | frameshift-variant, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211661 | TCACAACGGACATTA[-/C]TCCTCTTATGTCAAA | 100287144 |
| rs750298728 | snp | G/T | | | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212282 | ACCCACACGTAGGGG[G/T]GCATACACACACACA | 100287144 |
| rs750300799 | snp | C/G | 0.000355177 | 0.0133215 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211259 | ATTTGGAGGCTACTG[C/G]AGATCTCAAATCAAG | 100287144 |
| rs750425676 | snp | C/G | 9.79384e-05 | 0.00699711 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212255 | GTGCCAGTGATCTCA[C/G]TGGAAGTACCGACCC | 100287144 |
| rs750489969 | snp | A/G | | | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211660 | GTCACAACGGACATT[A/G]CTCCTCTTATGTCAA | 100287144 |
| rs750657136 | snp | A/C | 0.0201449 | 0.0983191 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210665 | AGTCGACATGGAGGA[A/C]GACTCACTCTACTTG | 100287144 |
| rs750694643 | snp | A/G | 0.00189573 | 0.030729 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211779 | CTCTTTTACATCCAG[A/G]AGAGTGAATGGGAAA | 100287144 |
| rs751055524 | snp | C/G | 9.77469e-05 | 0.00699027 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212242 | GGGCTCTGCTTGTGT[C/G]CCAGTGATCTCAGTG | 100287144 |
| rs751210524 | snp | A/G | 0.0055172 | 0.0522318 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211439 | TTGTCTCCAGAGGGC[A/G]CCGGCCTCCAAGACG | 100287144 |
| rs751211142 | snp | A/T | 0.00036036 | 0.0134183 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211231 | CTAAGGACACCACCC[A/T]CATCCACCAAATATT | 100287144 |
| rs751237133 | in-del | -/CA/CACA/CACACACACACACGCACACACA/GC | | | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212283 | CCACACGTAGGGGTG[lengthTooLong]CATACACACACACAC | 100287144 |
| rs751430396 | snp | C/T | 0.000290613 | 0.0120508 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211735 | CCGCCTCTAGCATCA[C/T]TTCTGTCCTGAGTCA | 100287144 |
| rs751449376 | snp | A/C | 0.000219974 | 0.0104852 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212159 | TCAGGAGTCCATGAA[A/C]ACTGGCACACTCGCT | 100287144 |
| rs751594413 | snp | G/T | 8.71346e-05 | 0.00659998 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210652 | TGATCCTTGTTCCAG[G/T]CGACATGGAGGACGA | 100287144 |
| rs751773860 | snp | G/T | 0.000495172 | 0.0157271 | stop-gained, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211653 | TGGAGTTGTCACAAC[G/T]GACATTACTCCTCTT | 100287144 |
| rs751973577 | snp | C/G | 0.000972605 | 0.0220308 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211946 | GGAAAGAGCCACTCA[C/G]GAAAGCACCTTAGAC | 100287144 |
| rs751994785 | snp | C/T | 0.000268565 | 0.0115849 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210971 | CAAACCGCCACTTGC[C/T]AACTACATGCTGTTC | 100287144 |
| rs752045864 | snp | C/T | 0.000470699 | 0.0153339 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212042 | TACGGTGCCTCCCGA[C/T]GTACTTGTGATTCAT | 100287144 |
| rs752146765 | snp | C/T | 0.000180326 | 0.00949372 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210901 | CGGTGGGGGCTGGGC[C/T]CCAGAATATGGGAAA | 100287144 |
| rs752232271 | snp | A/C/G | 0.00097167 | 0.0220232 | synonymous-codon, missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212072 | TCAATCAAAATACAA[A/C/G]TGTCGGATGAAGAAC | 100287144 |
| rs752343647 | snp | A/C | 0.000200844 | 0.0100191 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211099 | TCCAGCCCTCACAGG[A/C]ATTGGCTGCTGGCTT | 100287144 |
| rs752722875 | snp | A/C | 0.000142349 | 0.00843529 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211650 | GGGTGGAGTTGTCAC[A/C]ACGGACATTACTCCT | 100287144 |
| rs752807058 | snp | A/G | 0.000273013 | 0.0116804 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210878 | TCTGAGTAGCAGGAG[A/G]CCTGCTGCGGTGGGG | 100287144 |
| rs753146741 | snp | A/G | 0.000705965 | 0.0187746 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211931 | GGACGAGCACTTGGT[A/G]GAAAGAGCCACTCAG | 100287144 |
| rs753269470 | snp | A/C/T | 0.000591366 | 0.0171853 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211890 | GAGCTCAAGAGAGAC[A/C/T]ACCCCTGCCTCCAGG | 100287144 |
| rs753481579 | snp | A/C | 0.000238322 | 0.0109135 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212055 | GACGTACTTGTGATT[A/C]ATCAATCAAAATACA | 100287144 |
| rs753595602 | snp | A/G | 0.000162787 | 0.00902036 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212289 | CGTAGGGGTGCATAC[A/G]CACACACACACACAC | 100287144 |
| rs753755233 | snp | C/T | 0.000161199 | 0.00897628 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211556 | GCAATATCCTGAGTG[C/T]CTTGACATGCAGCCA | 100287144 |
| rs753810736 | snp | A/G | 7.51343e-05 | 0.00612874 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211454 | GCCGGCCTCCAAGAC[A/G]TTAACTTTACACAAC | 100287144 |
| rs753946107 | snp | C/T | 7.17695e-05 | 0.00598996 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211867 | CAGACAGGCGAGCAA[C/T]GCAAGGAGAGCTCAA | 100287144 |
| rs754133272 | snp | A/C | 0.000474046 | 0.0153883 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210768 | CAGCGTACTTCTCTC[A/C]CTGAGAAGTCACCAC | 100287144 |
| rs754279905 | snp | C/G | 0.00120555 | 0.0245218 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211805 | GGAAAGACACAGTGA[C/G]AGTGTGTCAAGAGGC | 100287144 |
| rs754287598 | snp | C/G | 0.000251162 | 0.0112035 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211209 | CACAAGCAGGTAGAT[C/G]GTCACTCTAAGGACA | 100287144 |
| rs754501727 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210579 | GCTCGTCATTTGAAG[A/G]CTCTCTCGGAAGAGA | 100287144 |
| rs754518564 | snp | A/G | 0.000169319 | 0.00919951 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211960 | AGGAAAGCACCTTAG[A/G]CCACTGGAAATTCCT | 100287144 |
| rs754678311 | snp | A/G | 0.000476815 | 0.0154331 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212056 | ACGTACTTGTGATTC[A/G]TCAATCAAAATACAA | 100287144 |
| rs754844247 | snp | A/C | 0.000161629 | 0.00898824 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212290 | GTAGGGGTGCATACA[A/C]ACACACACACACACA | 100287144 |
| rs754878042 | snp | A/C | 0.000243013 | 0.0110203 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211557 | CAATATCCTGAGTGC[A/C]TTGACATGCAGCCAT | 100287144 |
| rs755011622 | snp | C/G | 9.46656e-05 | 0.00687923 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210776 | TTCTCTCCCTGAGAA[C/G]TCACCACTCTCATGT | 100287144 |
| rs755103240 | snp | G/T | 0.00230216 | 0.0338493 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211868 | AGACAGGCGAGCAAC[G/T]CAAGGAGAGCTCAAG | 100287144 |
| rs755137673 | snp | A/T | 0.000548095 | 0.0165453 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210683 | CTCACTCTACTTGGG[A/T]GGTGAGTGGCAGTTC | 100287144 |
| rs755183482 | snp | A/G | 0.000241293 | 0.0109813 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212263 | GATCTCAGTGGAAGT[A/G]CCGACCCACACGTAG | 100287144 |
| rs755513343 | snp | A/T | 0.00116077 | 0.0240632 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211808 | AAGACACAGTGAGAG[A/T]GTGTCAAGAGGCAGG | 100287144 |
| rs755820623 | snp | A/C | 0.000157604 | 0.00887566 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211893 | CTCAAGAGAGACCAC[A/C]CCTGCCTCCAGGCCC | 100287144 |
| rs755890093 | snp | G/T | 9.81114e-05 | 0.00700329 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212257 | GCCAGTGATCTCAGT[G/T]GAAGTACCGACCCAC | 100287144 |
| rs755994452 | snp | A/C/T | 0.000529416 | 0.0162628 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211453 | CGCCGGCCTCCAAGA[A/C/T]GTTAACTTTACACAA | 100287144 |
| rs756005790 | snp | A/C | 0.000203376 | 0.010082 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212287 | CACGTAGGGGTGCAT[A/C]CACACACACACACAC | 100287144 |
| rs756047773 | snp | C/G/T | 0.00133067 | 0.0257598 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211274 | GAGATCTCAAATCAA[C/G/T]TGTCTCCACTGCCAC | 100287144 |
| rs756141121 | snp | C/G | 0.000394283 | 0.0140352 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211783 | TTTACATCCAGAAGA[C/G]TGAATGGGAAAGACA | 100287144 |
| rs756263370 | snp | A/C | 7.15948e-05 | 0.00598266 | stop-gained, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211661 | TCACAACGGACATTA[A/C]TCCTCTTATGTCAAA | 100287144 |
| rs756300417 | snp | A/T | 0.0103681 | 0.0712498 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210669 | GACATGGAGGACGAC[A/T]CACTCTACTTGGGAG | 100287144 |
| rs756767928 | snp | C/T | 0.000309358 | 0.0124332 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211108 | CACAGGCATTGGCTG[C/T]TGGCTTCCATAGAGG | 100287144 |
| rs756787218 | snp | C/T | 0.000365831 | 0.0135197 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211232 | TAAGGACACCACCCT[C/T]ATCCACCAAATATTT | 100287144 |
| rs756807376 | snp | C/T | 0.000195656 | 0.00988888 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212252 | TGTGTGCCAGTGATC[C/T]CAGTGGAAGTACCGA | 100287144 |
| rs757085733 | snp | C/T | 0.00017481 | 0.00934743 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210653 | GATCCTTGTTCCAGT[C/T]GACATGGAGGACGAC | 100287144 |
| rs757220099 | snp | A/T | 0.00010882 | 0.00737551 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212166 | TCCATGAACACTGGC[A/T]CACTCGCTTCCCTAC | 100287144 |
| rs757557936 | snp | A/C/T | 0.00101036 | 0.0224534 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211659 | TGTCACAACGGACAT[A/C/T]ACTCCTCTTATGTCA | 100287144 |
| rs757611606 | snp | A/C/G | 0.00122268 | 0.0247007 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211952 | AGCCACTCAGGAAAG[A/C/G]ACCTTAGACCACTGG | 100287144 |
| rs757794004 | snp | C/T | 0.000447608 | 0.0149534 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210974 | ACCGCCACTTGCCAA[C/T]TACATGCTGTTCCGG | 100287144 |
| rs757912781 | snp | C/G | 0.000224039 | 0.0105816 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212148 | ACCCCGACAGATCAG[C/G]AGTCCATGAACACTG | 100287144 |
| rs757971149 | snp | C/G | 8.98998e-05 | 0.00670386 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210993 | ATGCTGTTCCGGGAG[C/G]ACTCTCAAACGTGTC | 100287144 |
| rs758063854 | in-del | -/A | 0.000135529 | 0.0082308 | frameshift-variant, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211841 | CCAAGAGCCCTTGGC[-/A]GTAGAAGACACAGAC | 100287144 |
| rs758325004 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210372 | ATCCTGAGGAGTAAT[C/T]TGATTCAGGTGTTCT | 100287144 |
| rs758498723 | snp | A/G | 0.000218794 | 0.010457 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212293 | GGGGTGCATACACAC[A/G]CACACACACACACAC | 100287144 |
| rs758582719 | snp | C/T | 9.44956e-05 | 0.00687305 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211487 | TGCCAAGGTCCTCAT[C/T]CTTGTATTGAAGAGA | 100287144 |
| rs758854770 | snp | C/G | 0.000180963 | 0.00951045 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210893 | ACCTGCTGCGGTGGG[C/G]GCTGGGCTCCAGAAT | 100287144 |
| rs758937961 | snp | A/G | 0.00123198 | 0.0247886 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211722 | GATGCCGAGGTCACC[A/G]CCTCTAGCATCACTT | 100287144 |
| rs758949717 | snp | A/C/T | 0.000335627 | 0.0129499 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211942 | TGGTGGAAAGAGCCA[A/C/T]TCAGGAAAGCACCTT | 100287144 |
| rs759245501 | snp | A/G | 0.00084674 | 0.0205585 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210616 | CTTTCTGCAACCTGC[A/G]GTCCCAGCAGAAAAA | 100287144 |
| rs759473039 | snp | C/G/T | 0.00127353 | 0.0252059 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211647 | GCTGGGTGGAGTTGT[C/G/T]ACAACGGACATTACT | 100287144 |
| rs759609188 | snp | C/G | 0.000175608 | 0.00936873 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211922 | CCCCGAGTTGGACGA[C/G]CACTTGGTGGAAAGA | 100287144 |
| rs759637493 | snp | C/G | 0.0137692 | 0.0818229 | stop-gained, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210956 | GCAGTGCCTGACATA[C/G]AAACCGCCACTTGCC | 100287144 |
| rs759768856 | snp | A/T | 0.00138504 | 0.0262793 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212020 | TCAACGTCAGAAGAG[A/T]CGAAGGTACGGTGCC | 100287144 |
| rs759820148 | snp | A/T | 9.1781e-05 | 0.00677363 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210860 | TCCCAGGGAGAAGCC[A/T]CCTCTGAGTAGCAGG | 100287144 |
| rs759914455 | snp | C/T | 0.000168905 | 0.00918824 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211408 | TCAATGGAGAGAATG[C/T]CTATCATTGTGGTGT | 100287144 |
| rs760142831 | snp | A/C | 0.000197161 | 0.00992681 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211532 | AGGCAACAAAATTGC[A/C]AAGAATGTGCAATAT | 100287144 |
| rs760337018 | snp | A/G | 0.000253968 | 0.0112659 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211632 | GCTGTGCTGGTCCAC[A/G]CTGGGTGGAGTTGTC | 100287144 |
| rs760448839 | in-del | -/G | 0.000163026 | 0.00902698 | frameshift-variant, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211055 | CAAGCTCACATCACA[-/G]AGGGCCCTCCACATT | 100287144 |
| rs760504439 | in-del | -/ACAC | | | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212287 | CACGTAGGGGTGCAT[-/ACAC]ACACACACACACACA | 100287144 |
| rs760762526 | snp | A/C | 0.000351648 | 0.0132552 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211908 | CCCTGCCTCCAGGCC[A/C]CCGAGTTGGACGAGC | 100287144 |
| rs760961880 | snp | A/G | 0.00028748 | 0.0119857 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211861 | AAGACACAGACAGGC[A/G]AGCAACGCAAGGAGA | 100287144 |
| rs761121126 | snp | A/C | 0.000198275 | 0.00995481 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212200 | GGAGGACCAGGAGAT[A/C]CAAAGGGAAGAACAA | 100287144 |
| rs761225519 | snp | G/T | 0.000830565 | 0.0203615 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211382 | GGAACAGTTGGTGAA[G/T]CCCGAAGAACTCAAT | 100287144 |
| rs761280543 | snp | A/G | 0.000483598 | 0.0155424 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211205 | CGGGCACAAGCAGGT[A/G]GATCGTCACTCTAAG | 100287144 |
| rs761307734 | snp | C/G | 0.000201207 | 0.0100281 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212279 | CCGACCCACACGTAG[C/G]GGTGCATACACACAC | 100287144 |
| rs761384239 | snp | C/T | 0.000314787 | 0.0125417 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211440 | TGTCTCCAGAGGGCG[C/T]CGGCCTCCAAGACGT | 100287144 |
| rs761665154 | snp | A/G | 0.000867679 | 0.0208107 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211859 | AGAAGACACAGACAG[A/G]CGAGCAACGCAAGGA | 100287144 |
| rs761704435 | in-del | -/CG | | | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212295 | GTGCATACACACACA[-/CG]CACACACACACACAC | 100287144 |
| rs761757579 | in-del | -/C | 0.000386772 | 0.013901 | frameshift-variant, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211531 | CAGGCAACAAAATTG[-/C]CAAGAATGTGCAATA | 100287144 |
| rs761771458 | snp | C/T | 0.000372995 | 0.0136513 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210823 | TCTGTGATGATTTGG[C/T]TCCTGTGGCAAGACA | 100287144 |
| rs761896168 | snp | C/T | 0.00019478 | 0.00986671 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210756 | TTTGCTGAAATCCAG[C/T]GTACTTCTCTCCCTG | 100287144 |
| rs762077747 | snp | C/T | 0.00164338 | 0.028618 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211743 | AGCATCACTTCTGTC[C/T]TGAGTCAACAGGCCT | 100287144 |
| rs762229685 | snp | A/G | 0.000235849 | 0.0108567 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212043 | ACGGTGCCTCCCGAC[A/G]TACTTGTGATTCATC | 100287144 |
| rs762347070 | snp | C/G | 0.000106163 | 0.00728492 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210739 | CTCGGCCAGATGCAG[C/G]TTTTGCTGAAATCCA | 100287144 |
| rs762419341 | snp | A/T | 0.000120605 | 0.00776455 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212130 | CTAAACCTCTCTTCG[A/T]CGACCCCGACAGATC | 100287144 |
| rs762518628 | snp | C/T | 9.76134e-05 | 0.0069855 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212232 | CACAGCAAGAGGGCT[C/T]TGCTTGTGTGCCAGT | 100287144 |
| rs762619931 | snp | C/G | 0.000198216 | 0.00995333 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212274 | AAGTACCGACCCACA[C/G]GTAGGGGTGCATACA | 100287144 |
| rs762838497 | snp | A/C/T | 0.0002467 | 0.0111036 | missense, synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211652 | GTGGAGTTGTCACAA[A/C/T]GGACATTACTCCTCT | 100287144 |
| rs762996944 | snp | A/G | 0.00042647 | 0.0145963 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211729 | AGGTCACCGCCTCTA[A/G]CATCACTTCTGTCCT | 100287144 |
| rs763057815 | snp | C/T | 0.000842308 | 0.0205047 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212120 | AAGCTCCCTGCTAAA[C/T]CTCTCTTCGACGACC | 100287144 |
| rs763621145 | snp | G/T | 9.76038e-05 | 0.00698515 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212241 | AGGGCTCTGCTTGTG[G/T]GCCAGTGATCTCAGT | 100287144 |
| rs763630651 | snp | A/G | 0.00178944 | 0.0298583 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212275 | AGTACCGACCCACAC[A/G]TAGGGGTGCATACAC | 100287144 |
| rs763780401 | snp | C/G | 0.000351741 | 0.013257 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211230 | TCTAAGGACACCACC[C/G]TCATCCACCAAATAT | 100287144 |
| rs763893687 | in-del | -/TC | | | frameshift-variant, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211056 | AAGCTCACATCACAA[-/TC]GGGCCCTCCACATTC | 100287144 |
| rs763912960 | snp | C/T | 0.0027027 | 0.0366612 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211732 | TCACCGCCTCTAGCA[C/T]CACTTCTGTCCTGAG | 100287144 |
| rs763960231 | snp | A/G | 8.70436e-05 | 0.00659653 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210650 | TGTGATCCTTGTTCC[A/G]GTCGACATGGAGGAC | 100287144 |
| rs764640798 | snp | A/G | 0.000939518 | 0.0216536 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212040 | GGTACGGTGCCTCCC[A/G]ACGTACTTGTGATTC | 100287144 |
| rs764701065 | in-del | -/A | 0.000194288 | 0.00985425 | frameshift-variant, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211531 | AGGCAACAAAATTGC[-/A]CAAGAATGTGCAATA | 100287144 |
| rs764955218 | snp | A/C | 0.000348533 | 0.0131964 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212136 | CTCTCTTCGACGACC[A/C]CGACAGATCAGGAGT | 100287144 |
| rs765044789 | snp | A/C | 0.000299133 | 0.0122261 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211569 | TGCCTTGACATGCAG[A/C]CATACATGTCTCAGC | 100287144 |
| rs765235844 | snp | A/C | 0.000183604 | 0.00957958 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210861 | CCCAGGGAGAAGCCT[A/C]CTCTGAGTAGCAGGA | 100287144 |
| rs765358728 | snp | C/T | 0.000716846 | 0.0189185 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211925 | CGAGTTGGACGAGCA[C/T]TTGGTGGAAAGAGCC | 100287144 |
| rs765586859 | snp | G/T | 0.000250031 | 0.0111782 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211437 | GTTTGTCTCCAGAGG[G/T]CGCCGGCCTCCAAGA | 100287144 |
| rs765702559 | snp | C/T | 0.000150116 | 0.00866231 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211879 | CAACGCAAGGAGAGC[C/T]CAAGAGAGACCACCC | 100287144 |
| rs765812828 | snp | C/G | 0.000496155 | 0.0157427 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211642 | TCCACGCTGGGTGGA[C/G]TTGTCACAACGGACA | 100287144 |
| rs766003982 | in-del | -/TGCA | 0.000403714 | 0.0142019 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212282 | ACCCACACGTAGGGG[-/TGCA]TACACACACACACAC | 100287144 |
| rs766154256 | snp | C/G | 0.000320154 | 0.0126481 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212288 | ACGTAGGGGTGCATA[C/G]ACACACACACACACA | 100287144 |
| rs766267025 | snp | G/T | 0.000135888 | 0.0082417 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210857 | TGCTCCCAGGGAGAA[G/T]CCTCCTCTGAGTAGC | 100287144 |
| rs766331529 | snp | A/C | 0.000572246 | 0.0169055 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211864 | ACACAGACAGGCGAG[A/C]AACGCAAGGAGAGCT | 100287144 |
| rs766491498 | snp | C/G | 0.000227894 | 0.0106722 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210760 | CTGAAATCCAGCGTA[C/G]TTCTCTCCCTGAGAA | 100287144 |
| rs766606266 | snp | A/C | 0.000441794 | 0.014856 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211910 | CTGCCTCCAGGCCCC[A/C]GAGTTGGACGAGCAC | 100287144 |
| rs766716084 | snp | A/G | 0.00526774 | 0.0510502 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212228 | CAAACACAGCAAGAG[A/G]GCTCTGCTTGTGTGC | 100287144 |
| rs766786640 | snp | C/G | 0.000243398 | 0.011029 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211206 | GGGCACAAGCAGGTA[C/G]ATCGTCACTCTAAGG | 100287144 |
| rs766910530 | snp | C/G | 0.000391428 | 0.0139843 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211089 | GGCCATGTCATCCAG[C/G]CCTCACAGGCATTGG | 100287144 |
| rs766946531 | snp | C/T | 0.00154202 | 0.0277242 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211448 | GAGGGCGCCGGCCTC[C/T]AAGACGTTAACTTTA | 100287144 |
| rs767071507 | snp | C/G | | | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212281 | GACCCACACGTAGGG[C/G]TGCATACACACACAC | 100287144 |
| rs767409378 | snp | A/C/T | 0.0011611 | 0.0240666 | synonymous-codon, stop-gained, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211860 | GAAGACACAGACAGG[A/C/T]GAGCAACGCAAGGAG | 100287144 |
| rs767410415 | snp | C/T | 0.000151429 | 0.00870009 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212253 | GTGTGCCAGTGATCT[C/T]AGTGGAAGTACCGAC | 100287144 |
| rs767484628 | snp | A/G | 0.000532056 | 0.0163017 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210662 | TCCAGTCGACATGGA[A/G]GACGACTCACTCTAC | 100287144 |
| rs767608503 | snp | C/G | 0.00152416 | 0.0275637 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211747 | TCACTTCTGTCCTGA[C/G]TCAACAGGCCTACGT | 100287144 |
| rs767704518 | snp | A/C | 0.000179388 | 0.009469 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210981 | CTTGCCAACTACATG[A/C]TGTTCCGGGAGCACT | 100287144 |
| rs767922901 | snp | A/C/G/T | 0.00105163 | 0.0229119 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212135 | CCTCTCTTCGACGAC[A/C/G/T]CCGACAGATCAGGAG | 100287144 |
| rs768047557 | snp | G/T | 0.000118575 | 0.00769892 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212054 | CGACGTACTTGTGAT[G/T]CATCAATCAAAATAC | 100287144 |
| rs768086813 | snp | A/C | 0.00019115 | 0.00977437 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211076 | CCTCCACATTCCTGG[A/C]CATGTCATCCAGCCC | 100287144 |
| rs768265900 | snp | A/T | 0.000187073 | 0.00966962 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210808 | AGACCCGTGTCGACC[A/T]CTGTGATGATTTGGC | 100287144 |
| rs768381571 | snp | C/G | 0.000279603 | 0.0118205 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211303 | ACGGCATTTCAGACA[C/G]TTTTGACCCTTACCT | 100287144 |
| rs768386365 | in-del | -/ACACAC | 0.00671133 | 0.057538 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212287 | CACGTAGGGGTGCAT[-/ACACAC]ACACACACACACACA | 100287144 |
| rs768720329 | snp | G/T | 0.000400588 | 0.0141468 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212188 | CTTCCCTACGAGGGA[G/T]GACCAGGAGATCCAA | 100287144 |
| rs768735843 | snp | A/C | 6.85096e-05 | 0.00585236 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211857 | GTAGAAGACACAGAC[A/C]GGCGAGCAACGCAAG | 100287144 |
| rs768951312 | snp | G/T | 0.000164123 | 0.00905729 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211171 | TCACTGTGGATGCCA[G/T]GAGAAAGGCATGCCT | 100287144 |
| rs768954857 | snp | C/T | 0.000160914 | 0.00896834 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211688 | CAAAGCTCAAGAAGG[C/T]CAGTGGTATAAAATG | 100287144 |
| rs769044833 | snp | A/G | 0.000505561 | 0.015891 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211626 | CTCTATGCTGTGCTG[A/G]TCCACGCTGGGTGGA | 100287144 |
| rs769362755 | snp | A/T | 0.000215913 | 0.010388 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210737 | TTCTCGGCCAGATGC[A/T]GCTTTTGCTGAAATC | 100287144 |
| rs769415224 | snp | C/T | 0.00161681 | 0.0283865 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211724 | TGCCGAGGTCACCGC[C/T]TCTAGCATCACTTCT | 100287144 |
| rs769562747 | snp | C/G | 0.00021575 | 0.010384 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211154 | CCATGAATTTCTCAT[C/G]TTCACTGTGGATGCC | 100287144 |
| rs769612235 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210324 | TGTGGCCACTGTCCC[A/T]ACCCGGTTACACTCC | 100287144 |
| rs769616228 | snp | C/T | 0.000835509 | 0.020422 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212178 | GGCACACTCGCTTCC[C/T]TACGAGGGAGGACCA | 100287144 |
| rs769617915 | snp | C/T | 0.00328616 | 0.0404015 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211039 | GCATGCTCTGTACTA[C/T]GCAAGCTCACATCAC | 100287144 |
| rs769799650 | snp | C/T | 0.00011556 | 0.00760044 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212021 | CAACGTCAGAAGAGT[C/T]GAAGGTACGGTGCCT | 100287144 |
| rs770233386 | snp | A/T | 0.000502134 | 0.0158371 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211603 | ACACAGGACCTCTCG[A/T]CTATGTCCTCTATGC | 100287144 |
| rs770596700 | snp | C/T | 0.000226296 | 0.0106347 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211717 | TGGATGATGCCGAGG[C/T]CACCGCCTCTAGCAT | 100287144 |
| rs770655849 | snp | A/T | 0.000245369 | 0.0110736 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212085 | AAGTGTCGGATGAAG[A/T]ACCATCATCCTGAAC | 100287144 |
| rs770933193 | snp | G/T | 0.000369727 | 0.0135914 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211012 | CTCAAACGTGTCATC[G/T]TCACAAGGGCTGCAT | 100287144 |
| rs771174886 | snp | C/T | 0.00018655 | 0.00965609 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211494 | GTCCTCATCCTTGTA[C/T]TGAAGAGATTCCCCG | 100287144 |
| rs771365767 | snp | A/G | 0.00404923 | 0.0448132 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212297 | TGCATACACACACAC[A/G]CACACACACACACAC | 100287144 |
| rs771374725 | snp | A/G | 0.000187705 | 0.00968594 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210804 | TGTGAGACCCGTGTC[A/G]ACCTCTGTGATGATT | 100287144 |
| rs771589689 | snp | A/G/T | 0.00120943 | 0.0245612 | missense, stop-gained, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211386 | CAGTTGGTGAAGCCC[A/G/T]AAGAACTCAATGGAG | 100287144 |
| rs771703064 | snp | A/C | 0.000162483 | 0.00901193 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211902 | GACCACCCCTGCCTC[A/C]AGGCCCCCGAGTTGG | 100287144 |
| rs771751319 | snp | C/T | 0.000716204 | 0.01891 | stop-gained, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210942 | GTGAACGCTTCCCTG[C/T]AGTGCCTGACATACA | 100287144 |
| rs772113844 | snp | A/C | 0.00022477 | 0.0105988 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211194 | GCATGCCTTCCCGGG[A/C]ACAAGCAGGTAGATC | 100287144 |
| rs772162129 | snp | A/C | 0.000185977 | 0.00964127 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210832 | ATTTGGCTCCTGTGG[A/C]AAGACAGCTTGCTCC | 100287144 |
| rs772226220 | in-del | -/AGAT | 0.000275723 | 0.0117382 | frameshift-variant, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210858 | CTCCCAGGGAGAAGC[-/AGAT]CTCCTCTGAGTAGCA | 100287144 |
| rs772327209 | in-del | -/AC | 0.213305 | 0.247292 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212287 | CACGTAGGGGTGCAT[-/AC]ACACACACACACACA | 100287144 |
| rs772468549 | snp | A/C | 0.000411777 | 0.0143429 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210611 | AGCGTCTTTCTGCAA[A/C]CTGCGGTCCCAGCAG | 100287144 |
| rs772527028 | snp | A/T | 0.00492888 | 0.0493978 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211832 | AGGCAGGGAACCAAG[A/T]GCCCTTGGCGTAGAA | 100287144 |
| rs772843964 | snp | C/G | 0.000230317 | 0.0107287 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211628 | CTATGCTGTGCTGGT[C/G]CACGCTGGGTGGAGT | 100287144 |
| rs773021966 | snp | C/G | 0.000357718 | 0.013369 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210948 | GCTTCCCTGCAGTGC[C/G]TGACATACAAACCGC | 100287144 |
| rs773076982 | snp | A/G | 0.00176642 | 0.0296663 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211994 | AGAGCAAAACAAAAC[A/G]AAGCCTGAGTTCAAC | 100287144 |
| rs773093882 | snp | A/C | 0.000664452 | 0.0182149 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211906 | ACCCCTGCCTCCAGG[A/C]CCCCGAGTTGGACGA | 100287144 |
| rs773336496 | snp | C/G | 0.000369788 | 0.0135925 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210844 | TGGCAAGACAGCTTG[C/G]TCCCAGGGAGAAGCC | 100287144 |
| rs773432920 | snp | A/G | 0.000895656 | 0.021143 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211362 | CAGAGTGTCCAGCAA[A/G]CTTTGGAACAGTTGG | 100287144 |
| rs773845773 | snp | G/T | 8.0707e-05 | 0.00635193 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212266 | CTCAGTGGAAGTACC[G/T]ACCCACACGTAGGGG | 100287144 |
| rs773847461 | snp | A/C | 8.04991e-05 | 0.00634374 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211200 | CTTCCCGGGCACAAG[A/C]AGGTAGATCGTCACT | 100287144 |
| rs773898909 | snp | A/G | 0.000128353 | 0.00801 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212194 | TACGAGGGAGGACCA[A/G]GAGATCCAAAGGGAA | 100287144 |
| rs774030846 | snp | G/T | 0.000705254 | 0.0187651 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212276 | GTACCGACCCACACG[G/T]AGGGGTGCATACACA | 100287144 |
| rs774242589 | snp | C/G | 0.000164298 | 0.00906212 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211172 | CACTGTGGATGCCAT[C/G]AGAAAGGCATGCCTT | 100287144 |
| rs774424041 | snp | A/G | 0.000179281 | 0.00946617 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210754 | CTTTTGCTGAAATCC[A/G]GCGTACTTCTCTCCC | 100287144 |
| rs774479089 | snp | A/G | 0.000138552 | 0.00832207 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211858 | TAGAAGACACAGACA[A/G]GCGAGCAACGCAAGG | 100287144 |
| rs774490556 | snp | A/C/T | 0.000472594 | 0.015366 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211073 | GGCCCTCCACATTCC[A/C/T]GGCCATGTCATCCAG | 100287144 |
| rs774513208 | in-del | -/CA | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210231 | ACACACAAACACACT[-/CA]CACACACACACACAC | 100287144 |
| rs774905374 | snp | A/C | 0.000239664 | 0.0109442 | stop-gained, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212128 | TGCTAAACCTCTCTT[A/C]GACGACCCCGACAGA | 100287144 |
| rs775068965 | snp | A/G | 0.000134608 | 0.00820279 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211844 | AAGAGCCCTTGGCGT[A/G]GAAGACACAGACAGG | 100287144 |
| rs775150733 | snp | A/C | 0.000195274 | 0.00987922 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212230 | AACACAGCAAGAGGG[A/C]TCTGCTTGTGTGCCA | 100287144 |
| rs775278423 | snp | C/T | 0.000273336 | 0.0116873 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211726 | CCGAGGTCACCGCCT[C/T]TAGCATCACTTCTGT | 100287144 |
| rs775353800 | in-del | -/GC | 0.000160565 | 0.00895862 | frameshift-variant, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211050 | CTATGCAAGCTCACA[-/GC]TCACAAGGGCCCTCC | 100287144 |
| rs775621966 | snp | A/C | 0.000241255 | 0.0109804 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212118 | CAAAGCTCCCTGCTA[A/C]ACCTCTCTTCGACGA | 100287144 |
| rs775684356 | snp | C/T | 0.000275166 | 0.0117264 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211045 | TCTGTACTATGCAAG[C/T]TCACATCACAAGGGC | 100287144 |
| rs775720120 | snp | C/T | 0.00594735 | 0.0542061 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211508 | ATTGAAGAGATTCCC[C/T]GATGTCACAGGCAAC | 100287144 |
| rs775737502 | snp | C/T | 0.000178827 | 0.00945418 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210960 | TGCCTGACATACAAA[C/T]CGCCACTTGCCAACT | 100287144 |
| rs775872683 | snp | G/T | 0.000504796 | 0.015879 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211614 | CTCGTCTATGTCCTC[G/T]ATGCTGTGCTGGTCC | 100287144 |
| rs776038865 | snp | G/T | 0.000247862 | 0.0111297 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211643 | CCACGCTGGGTGGAG[G/T]TGTCACAACGGACAT | 100287144 |
| rs776241734 | snp | A/G | 0.00018134 | 0.00952036 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211021 | GTCATCGTCACAAGG[A/G]CTGCATGCTCTGTAC | 100287144 |
| rs776263711 | snp | A/G | 0.000172995 | 0.00929881 | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210614 | GTCTTTCTGCAACCT[A/G]CGGTCCCAGCAGAAA | 100287144 |
| rs776395118 | snp | A/C | 0.000241867 | 0.0109943 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211720 | ATGATGCCGAGGTCA[A/C]CGCCTCTAGCATCAC | 100287144 |
| rs776491530 | snp | C/T | 0.000178875 | 0.00945545 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210952 | CCCTGCAGTGCCTGA[C/T]ATACAAACCGCCACT | 100287144 |
| rs776507098 | in-del | -/T | 0.000167056 | 0.00913785 | frameshift-variant, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211245 | CTCATCCACCAAATA[-/T]TTGGAGGCTACTGGA | 100287144 |
| rs776820384 | snp | A/G | 0.00128257 | 0.0252911 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212017 | AGTTCAACGTCAGAA[A/G]AGTCGAAGGTACGGT | 100287144 |
| rs776882180 | snp | G/T | 0.000352703 | 0.013275 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211914 | CTCCAGGCCCCCGAG[G/T]TGGACGAGCACTTGG | 100287144 |
| rs776892716 | snp | C/T | 9.86436e-05 | 0.00702226 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212272 | GGAAGTACCGACCCA[C/T]ACGTAGGGGTGCATA | 100287144 |
| rs777109520 | snp | G/T | 0.00163315 | 0.0285291 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211106 | CTCACAGGCATTGGC[G/T]GCTGGCTTCCATAGA | 100287144 |
| rs777162693 | snp | A/G | 0.000220459 | 0.0104967 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212157 | GATCAGGAGTCCATG[A/G]ACACTGGCACACTCG | 100287144 |
| rs777273706 | snp | A/G | 0.000558036 | 0.0166945 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211496 | CCTCATCCTTGTATT[A/G]AAGAGATTCCCCGAT | 100287144 |
| rs777359103 | snp | C/T | 0.00233624 | 0.0340978 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210997 | TGTTCCGGGAGCACT[C/T]TCAAACGTGTCATCG | 100287144 |
| rs777952240 | snp | C/T | 0.000188626 | 0.00970965 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211488 | GCCAAGGTCCTCATC[C/T]TTGTATTGAAGAGAT | 100287144 |
| rs778005245 | snp | A/G | 0.000746627 | 0.0193069 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212295 | GGTGCATACACACAC[A/G]CACACACACACACAC | 100287144 |
| rs778072185 | snp | A/C | 9.43174e-05 | 0.00686657 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210785 | TGAGAAGTCACCACT[A/C]TCATGTGAGACCCGT | 100287144 |
| rs778110528 | snp | C/G | 0.000171984 | 0.00927159 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211579 | TGCAGCCATACATGT[C/G]TCAGCAGAACACAGG | 100287144 |
| rs778214353 | snp | A/C/T | 0.000885435 | 0.0210253 | missense, synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211892 | GCTCAAGAGAGACCA[A/C/T]CCCTGCCTCCAGGCC | 100287144 |
| rs778231352 | snp | C/T | 0.000180489 | 0.009498 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210900 | GCGGTGGGGGCTGGG[C/T]TCCAGAATATGGGAA | 100287144 |
| rs778521129 | snp | A/T | 0.000119725 | 0.00773615 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212061 | CTTGTGATTCATCAA[A/T]CAAAATACAAGTGTC | 100287144 |
| rs778576705 | snp | C/T | 0.000475964 | 0.0154193 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211965 | AGCACCTTAGACCAC[C/T]GGAAATTCCTTCAAG | 100287144 |
| rs778590040 | snp | A/G | 0.0015447 | 0.0277482 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211479 | CACAACTCTGCCAAG[A/G]TCCTCATCCTTGTAT | 100287144 |
| rs778680956 | snp | C/T | 0.000179549 | 0.00947325 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210987 | AACTACATGCTGTTC[C/T]GGGAGCACTCTCAAA | 100287144 |
| rs778999172 | snp | C/T | 4.01518e-05 | 0.00448043 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212264 | ATCTCAGTGGAAGTA[C/T]CGACCCACACGTAGG | 100287144 |
| rs779000894 | snp | A/G | 0.000158907 | 0.00891224 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212291 | TAGGGGTGCATACAC[A/G]CACACACACACACAC | 100287144 |
| rs779021563 | in-del | -/AT | 0.000666148 | 0.0182382 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212285 | CACACGTAGGGGTGC[-/AT]ACACACACACACACA | 100287144 |
| rs779024677 | snp | A/C/G | 0.000283523 | 0.0119035 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210780 | CTCCCTGAGAAGTCA[A/C/G]CACTCTCATGTGAGA | 100287144 |
| rs779196105 | snp | C/T | 0.000183993 | 0.00958971 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211325 | CCCTTACCTGGACAT[C/T]GCCCTGGATATCCAG | 100287144 |
| rs779203229 | snp | C/T | 0.00111857 | 0.0236227 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211810 | GACACAGTGAGAGTG[C/T]GTCAAGAGGCAGGGA | 100287144 |
| rs779256287 | snp | A/G/T | 0.00109309 | 0.0233528 | stop-gained, missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211694 | TCAAGAAGGCCAGTG[A/G/T]TATAAAATGGATGAT | 100287144 |
| rs779364491 | snp | C/G | 0.000399441 | 0.0141266 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210695 | GGGAGGTGAGTGGCA[C/G]TTCAACCACTTTTCA | 100287144 |
| rs779661513 | snp | C/T | 0.000595415 | 0.0172439 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211895 | CAAGAGAGACCACCC[C/T]TGCCTCCAGGCCCCC | 100287144 |
| rs779721912 | snp | A/G/T | 0.00167884 | 0.0289261 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212261 | GTGATCTCAGTGGAA[A/G/T]TACCGACCCACACGT | 100287144 |
| rs779799607 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210352 | TCCTATTATATGTGC[C/T]TATCATCCTGAGGAG | 100287144 |
| rs779836601 | snp | A/G | 0.000214915 | 0.0103639 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211165 | TCATGTTCACTGTGG[A/G]TGCCATGAGAAAGGC | 100287144 |
| rs780110593 | snp | C/T | 0.000550206 | 0.0165771 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210674 | GGAGGACGACTCACT[C/T]TACTTGGGAGGTGAG | 100287144 |
| rs780235260 | snp | A/T | 0.00432401 | 0.0462959 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211788 | ATCCAGAAGAGTGAA[A/T]GGGAAAGACACAGTG | 100287144 |
| rs780625009 | snp | C/T | 0.000642261 | 0.0179086 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211253 | CCAAATATTTGGAGG[C/T]TACTGGAGATCTCAA | 100287144 |
| rs780704674 | snp | G/T | 0.00148976 | 0.0272518 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211833 | GGCAGGGAACCAAGA[G/T]CCCTTGGCGTAGAAG | 100287144 |
| rs780914401 | snp | A/T | 0.000642123 | 0.0179067 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212170 | TGAACACTGGCACAC[A/T]CGCTTCCCTACGAGG | 100287144 |
| rs780971715 | snp | C/T | 0.000157072 | 0.00886067 | synonymous-codon, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212108 | TCCTGAACAGCAAAG[C/T]TCCCTGCTAAACCTC | 100287144 |
| rs781041896 | snp | A/C | | | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212110 | CTGAACAGCAAAGCT[A/C]CCTGCTAAACCTCTC | 100287144 |
| rs781152906 | snp | A/C | 0.00149015 | 0.0272554 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9211125 | GGCTTCCATAGAGGC[A/C]AGCAGGAAGATGCCC | 100287144 |
| rs781662098 | snp | C/G | 0.00026936 | 0.0116021 | missense, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9210923 | TATGGGAAATACCTG[C/G]TACGTGAACGCTTCC | 100287144 |
| rs781748319 | snp | C/G | 0.000209688 | 0.0102372 | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212298 | GCATACACACACACA[C/G]ACACACACACACACA | 100287144 |
| rs796204091 | in-del | -/GC | | | downstream-variant-500B, intron-variant | USP17L10, FAM86KP | GRCh38.p7 | 4:9212283 | CCCACACGTAGGGGT[-/GC]ATACACACACACACA | 100287144 |