SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs368897260 | snp | C/T | 6.606e-05 | 0.00574679 | synonymous-codon | USP14 | GRCh38.p7 | 18:211185 | CGTAACACCAGAAGA[C/T]ATCTTACGGCTTTCT | 9097 |
rs368933428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:203755 | GCTGGGACTACAGGC[A/G]CCCGCCACCGTGCCC | 9097 |
rs369122052 | snp | A/G | 1.66164e-05 | 0.00288235 | intron-variant | USP14 | GRCh38.p7 | 18:197708 | AGAGGTAATTGAAAT[A/G]TATTTGTGATTATAG | 9097 |
rs369203116 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:206570 | CCAGTCTATTTTTTT[-/T]CTTTAGTTGCTTGTG | 9097 |
rs369246343 | in-del | -/TATG | 0.00597247 | 0.0543191 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213736 | CTAAAGGGAAATGCT[-/TATG]TATGTGGGAACAAGA | 9097 |
rs369247675 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:195245 | TTGTTAAAATGTAGG[C/T]TTTTATTTAAAAAAA | 9097 |
rs369296322 | snp | C/T | 3.30256e-05 | 0.00406346 | missense | USP14 | GRCh38.p7 | 18:197671 | AACAGAAATTGGAAG[C/T]AATAGAGGATGATTC | 9097 |
rs369297431 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:176227 | TGCTTTCTTTCTTTC[A/T]ACTTCGGTTTTAAAT | 9097 |
rs369300000 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:186426 | ATGCCACTGCACTCC[A/C]GCCTGGGCAATGCAA | 9097 |
rs369334281 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:203628 | TTTCTTTTTTTTTTT[G/T]AGACGGAGTCTCGCT | 9097 |
rs369344283 | snp | A/T | 1.90449e-05 | 0.00308579 | intron-variant | USP14 | GRCh38.p7 | 18:179067 | ATTTTATGTGTTTGA[A/T]CACTACTTTTTGAAG | 9097 |
rs369416345 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP14 | GRCh38.p7 | 18:210833 | CTCCTGTTAGTGTTC[A/G]CATTCAGTCTGTTGC | 9097 |
rs369429031 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:191257 | GTGAATTATTGTGTA[C/T]TGAAAAATTAAGAAA | 9097 |
rs369465567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:160855 | TATTCAAACCAGACT[A/G]AAGTGGCCTTTATGA | 9097 |
rs369467275 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:169300 | TGGGAGGCGGAGGTT[C/G]CAGTGAGCTGAGATC | 9097 |
rs369473697 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:206194 | AAGGTGAGACTGATT[C/T]ACTTTCTCTGCATTC | 9097 |
rs369481965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:173030 | CTTCGCCTGTGCCAA[A/G]TTTACAAGATTTTTT | 9097 |
rs369491896 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157454 | CAACAGTGTTCACAG[C/T]GTCTTCACCAGGAGT | 9097 |
rs369556622 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP14 | GRCh38.p7 | 18:200031 | CATATGCTAACAAAT[A/G]TTGGGACATCTCACT | 9097 |
rs369572061 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:188840 | CCGCCACTATGCCCA[A/G]CTAATTTTTTGTATT | 9097 |
rs369723288 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:205100 | AGGCTAGTCTCGAAC[C/T]CCTGAGCTCAGGCGA | 9097 |
rs369804135 | snp | C/G | 0.000228859 | 0.0106947 | intron-variant | USP14 | GRCh38.p7 | 18:163266 | GTCTGTAAATCTTGT[C/G]TTGTTATTTTTTAAT | 9097 |
rs369901616 | snp | C/T | 3.30311e-05 | 0.0040638 | intron-variant | USP14 | GRCh38.p7 | 18:192800 | ATTTGAGTGTTAGAA[C/T]GAATTGAATTCTATT | 9097 |
rs369902054 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:160541 | AAAATAAACACACAC[C/T]TGTGCCTCTTATAGA | 9097 |
rs369934427 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:201198 | AACATCTAGATATTT[C/G]AAGAAGGGCCTGGAG | 9097 |
rs369941964 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:195830 | CTAAACAGAGGTTAT[A/G]TGTTCTTTGTACTGA | 9097 |
rs369953991 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:184602 | CTACAAAACAGACAA[A/G]CAAACAAAAAACCAA | 9097 |
rs370023583 | in-del | -/T | 0.261056 | 0.249755 | intron-variant | USP14 | GRCh38.p7 | 18:169484 | AAAATGATGGTGTGA[-/T]TTTTTTTTTCTTTTT | 9097 |
rs370096899 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:169818 | CATTTTCATTACTCT[C/G]ATGTCAAGTATGTTG | 9097 |
rs370117151 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:174626 | TTTTTTTTTTTTTTT[A/T]AAAGACGAGGTCTTG | 9097 |
rs370161815 | snp | G/T | | | missense | USP14 | GRCh38.p7 | 18:163330 | AAAATGGGGAAAGGA[G/T]AAATTTGAAGGTGTA | 9097 |
rs370175580 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:177255 | GCTCTTGAGACAGTT[G/T]TCTTTGGAAAAAGAT | 9097 |
rs370293227 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212069 | TGACCTCAAGTCTTT[C/T]GTCTTCTGAGTGTTG | 9097 |
rs370358288 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:185480 | GTCTGTTAACACTAG[C/T]GTCTCATTCAGTTCA | 9097 |
rs370373107 | snp | A/G | 1.68221e-05 | 0.00290014 | missense | USP14 | GRCh38.p7 | 18:199279 | TTAGCTGTTTTATCA[A/G]TCAGGAAGTCAAGTA | 9097 |
rs370457822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:158869 | ACCCAGGCACCGTCC[C/T]CTCTCCCGGCTGGGT | 9097 |
rs370481000 | snp | A/G | 6.7457e-05 | 0.00580723 | intron-variant | USP14 | GRCh38.p7 | 18:210358 | TCTATTCATTGTCTA[A/G]TATTAATGGATTTAC | 9097 |
rs370518955 | snp | C/T | 1.64751e-05 | 0.00287007 | synonymous-codon | USP14 | GRCh38.p7 | 18:196696 | ATTCCACCTATTATT[C/T]TACTGCAGTTTTTGC | 9097 |
rs370545182 | snp | A/G | 1.65263e-05 | 0.00287452 | intron-variant | USP14 | GRCh38.p7 | 18:198160 | GCCAAGATATAGACT[A/G]TACTCATACCTTATT | 9097 |
rs370579645 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:209790 | TTATATTGTTGAAGT[A/G]TAGGACTGCTGGGTT | 9097 |
rs370692336 | snp | C/T | | | intron-variant, synonymous-codon | USP14 | GRCh38.p7 | 18:178989 | AGAAGAACCCTCAGC[C/T]AAAACTGTCTTCGTA | 9097 |
rs370733178 | snp | C/T | 4.9802e-05 | 0.00498984 | intron-variant | USP14 | GRCh38.p7 | 18:202993 | CGCTTCACTGAAATA[C/T]TTCCAGTTAATTAAT | 9097 |
rs370827011 | snp | A/G | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212853 | TTATCATAACATCTC[A/G]TATCTTTGTGTATGT | 9097 |
rs370840175 | in-del | -/A | | | intron-variant | USP14 | GRCh38.p7 | 18:196523 | CCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAT | 9097 |
rs370848583 | in-del | -/TTCT | | | intron-variant | USP14 | GRCh38.p7 | 18:210782 | TACATTTTTATGTCT[-/TTCT]GTTGTCTGGCTTAAA | 9097 |
rs370881616 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:179289 | TTCAGACTTCCAAGT[A/G]AATTTACTTAGGCTT | 9097 |
rs370894444 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:158936 | AGCCACCGATGGGTG[C/G]GGGGAGTGGAGATGG | 9097 |
rs370896806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:173675 | TGATCCGCCCACCTC[A/G]GCCTCCCAAAGTGCT | 9097 |
rs370992860 | snp | C/T | 4.95282e-05 | 0.00497611 | missense | USP14 | GRCh38.p7 | 18:211192 | CCAGAAGATATCTTA[C/T]GGCTTTCTGGTGGTG | 9097 |
rs371023410 | in-del | -/ACTATTACTATTT | | | intron-variant | USP14 | GRCh38.p7 | 18:179373 | ACTATATAAGTATTT[-/ACTATTACTATTT]TATGAGAAAACAGGG | 9097 |
rs371076284 | in-del | -/AC | | | intron-variant | USP14 | GRCh38.p7 | 18:209908 | TGAAATTGAACACTT[-/AC]AGAGAATTCAAATTT | 9097 |
rs371155458 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:211002 | TGTGGTCACTGGGTC[A/G]CACTTGGAGGACTGT | 9097 |
rs371171342 | snp | A/G | 1.65072e-05 | 0.00287286 | intron-variant | USP14 | GRCh38.p7 | 18:192813 | AATGAATTGAATTCT[A/G]TTGTTTAACTCGGCT | 9097 |
rs371177082 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:179616 | TCCTTGAGATGGGGT[C/T]TTGCTCTGTCACCCC | 9097 |
rs371226123 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:164635 | ATTTTTGTATTTTTA[A/G]TAGAGATGGGGTTTC | 9097 |
rs371229827 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:180614 | TAGCCCTAGCCAACC[A/G]TTCATCTACTTTCTG | 9097 |
rs371312622 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:197325 | TTACTGTTTCCATCC[C/T]GCTTTTTTTCGCTTC | 9097 |
rs371358855 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:170027 | ACCCTACAGGCTGAG[C/T]GCGGTGGCTCACACC | 9097 |
rs371367121 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | USP14 | GRCh38.p7 | 18:192954 | GACATTCTATTTTTC[A/G]CTCACAATCCTTTGC | 9097 |
rs371370107 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:194529 | TTTTTCCGTTATGCA[C/T]GTAATTTTTTTCTGA | 9097 |
rs371434515 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | USP14 | GRCh38.p7 | 18:159792 | TTCCTCAAAATGCCA[G/T]CGCTGACCAGAGTTT | 9097 |
rs371507130 | in-del | -/TATTTTATTT | | | intron-variant | USP14 | GRCh38.p7 | 18:200793 | TTGTTTATTTTATTT[-/TATTTTATTT]ATTTATTTACTTATT | 9097 |
rs371513227 | in-del | -/AT | 0.00260672 | 0.0360078 | intron-variant | USP14 | GRCh38.p7 | 18:204539 | TAAATGTGTTTACAC[-/AT]GTTTTTTGTTTGTTT | 9097 |
rs371665866 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:156490 | AAAATAAAGCTATCC[A/G]TAGCCTGCTATTCTA | 9097 |
rs371705703 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:172153 | TGAGGCAGTAGGATC[A/G]CTTAAGCCTAGGAGT | 9097 |
rs371870838 | snp | G/T | 5.73006e-05 | 0.00535229 | intron-variant | USP14 | GRCh38.p7 | 18:199344 | TCAGTCCATCCTTGT[G/T]GTTTGTGAATTCCAT | 9097 |
rs371886849 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:176109 | ATGATTTGTCTGTTT[-/T]CCTCTATCATCAAGC | 9097 |
rs371951378 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:188457 | TTAAAAGGATTTTTT[-/T]GGGGTCATTTGTTAG | 9097 |
rs371969303 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:160650 | TGAGCAAAAAGTTTT[A/C]AGTAACTTGCTCATG | 9097 |
rs372033166 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:195380 | CTTTGTGCTAAGATG[C/T]TGTATTTGGTGGGTT | 9097 |
rs372047009 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:180859 | GTATTTCATGGTTCA[C/T]TCACGTTACAGCACA | 9097 |
rs372108424 | in-del | -/AT | 0.00755907 | 0.0610114 | intron-variant | USP14 | GRCh38.p7 | 18:159491 | AAAATGGCACCTAAA[-/AT]ATGTGTGGTGTCTCC | 9097 |
rs372129870 | snp | A/G | 4.98318e-05 | 0.00499133 | intron-variant | USP14 | GRCh38.p7 | 18:197607 | ACTTTGTCTTTTTTT[A/G]CATTACAGGATGCTA | 9097 |
rs372258751 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:196005 | TTGAGAGTCCAACAA[C/T]TGTCAAAGAGTAGAT | 9097 |
rs372272692 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:164498 | TTGCCCTGTTGCCCA[G/T]GCTGGAGTGCAGTGG | 9097 |
rs372364293 | snp | A/T | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:213972 | ATGGACAAGATAGAT[A/T]GATTAGATAGATAGA | 9097 |
rs372491800 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:186535 | AGGCGGGCAGATCAC[C/T]GAAGGTCAGGAGTTC | 9097 |
rs372517405 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | USP14 | GRCh38.p7 | 18:170840 | GGGAGGAGAACAGCA[C/T]ACACGGGGGCCTGTC | 9097 |
rs372576211 | snp | A/T | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214007 | TAGATAGATGATGAT[A/T]GATTGATGATTGATA | 9097 |
rs372608565 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP14 | GRCh38.p7 | 18:173362 | GTGATCAGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 9097 |
rs372680136 | in-del | -/ACTT | | | intron-variant | USP14 | GRCh38.p7 | 18:208727 | TGACAGAACACACTT[-/ACTT]GATTTAAATTCTATT | 9097 |
rs372701346 | snp | C/T | 0.000153988 | 0.00877328 | missense | USP14 | GRCh38.p7 | 18:210389 | ATCTTTCTTTAGATA[C/T]TGGCTCCAATAATTG | 9097 |
rs372740570 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP14 | GRCh38.p7 | 18:168948 | CGTGCATGGTGGCAG[A/G]TGCCTGTAGTCCCAG | 9097 |
rs372757246 | in-del | -/A | 0.193028 | 0.243422 | intron-variant | USP14 | GRCh38.p7 | 18:168907 | AACTCCGTCTCTACT[-/A]AAAAAAAAAATACAA | 9097 |
rs372814489 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:166046 | ACATATTGAAAGGAA[A/G]GTATATACTTGCTTT | 9097 |
rs372860330 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:187923 | ATGAGGAAATAAGGC[A/G]TATTTTCTATTAGTA | 9097 |
rs372953435 | snp | C/T | 3.31159e-05 | 0.00406901 | intron-variant | USP14 | GRCh38.p7 | 18:166839 | GTATTATCTTATGAA[C/T]GTTTATTATAATGCA | 9097 |
rs373119413 | snp | C/T | 0.000214711 | 0.010359 | intron-variant | USP14 | GRCh38.p7 | 18:204734 | TCTTAATATCTTAAT[C/T]TCCCATCAGTGCTCA | 9097 |
rs373139406 | snp | A/G | 1.6623e-05 | 0.00288292 | missense | USP14 | GRCh38.p7 | 18:209986 | AGTGACAAAAAGAGT[A/G]GTCCCCAGAAAGAAG | 9097 |
rs373148270 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | USP14 | GRCh38.p7 | 18:203632 | TTTTTTTTTTTGAGA[A/C/T]GGAGTCTCGCTCTGT | 9097 |
rs373172404 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:173187 | GATCTCGGCTCACTG[C/T]AAGCTCCACCTCCTG | 9097 |
rs373310210 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:161624 | CCCAATGCTTTGTAC[C/T]GGGCTTGTCATTAAA | 9097 |
rs373319911 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:177672 | ACTTCTGGTCCTACC[A/T]TTTACTTTGTCTCAT | 9097 |
rs373357395 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:177459 | ATTCTGTAGTGATGG[C/G]TTAGTACTGCTTTAC | 9097 |
rs373370179 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:204812 | ATACTTTGTATAGTA[A/T]TATTTGGATCAATCT | 9097 |
rs373421008 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:198333 | ACCTCCACCTCCTGG[A/G]TTCAAACAGTTCTGC | 9097 |
rs373445010 | in-del | -/T | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:156785 | CTATACTGTAGTCTA[-/T]TTTAGTGTCAAGGCT | 9097 |
rs373489023 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:160069 | GCTCTTTGGGAGGCT[C/T]GAGGCGGGCGGATCA | 9097 |
rs373502995 | in-del | -/TATATAT | | | intron-variant | USP14 | GRCh38.p7 | 18:171027 | AAAAAAAAAAAAAAA[-/TATATAT]ATATATATATATATA | 9097 |
rs373511626 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:186677 | TGGGTCGCTTGAACC[A/C]GGGAGCAGAGGCTGC | 9097 |
rs373536207 | snp | C/T | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:211886 | TAATAGTACCTTTGA[C/T]TATACATTTATTATT | 9097 |
rs373649012 | snp | C/T | 0.000628037 | 0.0177094 | intron-variant | USP14 | GRCh38.p7 | 18:198165 | GATATAGACTATACT[C/T]ATACCTTATTAGAAT | 9097 |
rs373715268 | snp | A/G | 0.000287189 | 0.0119796 | intron-variant | USP14 | GRCh38.p7 | 18:210515 | GGTATTCTTTTTTCA[A/G]CTGTTCAATATTATT | 9097 |
rs373726844 | snp | A/C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:165312 | GGGTTAGATAAAATG[A/C/G]TAAAGATCTATAGTT | 9097 |
rs373972419 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:162828 | TTTGAGATGGAGTCT[C/T]GCACTGTCGCCCAGG | 9097 |
rs374016989 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:161296 | CTTCCAGTTTCATCT[A/G]CTGCTGCTTTCCCTT | 9097 |
rs374020562 | in-del | -/AT | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213123 | ATGATTCATGTATAT[-/AT]TTGTATGATGCTTGT | 9097 |
rs374063384 | in-del | -/GTA | | | intron-variant | USP14 | GRCh38.p7 | 18:195382 | TGTGCTAAGATGCTG[-/GTA]TATTTGGTGGGTTCA | 9097 |
rs374095270 | snp | A/T | | | intron-variant, missense | USP14 | GRCh38.p7 | 18:179011 | GTCTTCGTAGAAGAC[A/T]TGACAGAAGAACAGT | 9097 |
rs374129074 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | USP14 | GRCh38.p7 | 18:208713 | TGATGCCATTGTGGT[A/G]ACAGAACACACTTAC | 9097 |
rs374136811 | snp | A/G | 0.00443036 | 0.0468567 | intron-variant | USP14 | GRCh38.p7 | 18:158749 | CGCGCGCAGCACACC[A/G]GACCGGCGCTAGGCC | 9097 |
rs374155673 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:179631 | CTTGCTCTGTCACCC[C/T]GGCTGGAGTGCAGTG | 9097 |
rs374205732 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:207218 | GACTTGATTACTGTA[C/G]TTTTCTAATAAGGCT | 9097 |
rs374208209 | snp | C/T | 8.80382e-05 | 0.00663411 | intron-variant | USP14 | GRCh38.p7 | 18:211109 | TGCATAACATTAATT[C/T]ATCTTCTTGTCCCTG | 9097 |
rs374225342 | in-del | -/TTC | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213680 | CAGTAGCCCTTCTTC[-/TTC]AGGATTAAAAACGAT | 9097 |
rs374232333 | snp | G/T | 5.03918e-05 | 0.0050193 | intron-variant | USP14 | GRCh38.p7 | 18:197586 | CATTCACTGCCAGGA[G/T]TACTTACTTTGTCTT | 9097 |
rs374288739 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:159094 | CAGTGGTCGCCGTGG[A/G]AGGGAGCGGGGAAGA | 9097 |
rs374300842 | snp | A/G | 1.65072e-05 | 0.00287286 | missense | USP14 | GRCh38.p7 | 18:198131 | GTTGAGTTTGAAACT[A/G]CGTATCCTTATGAGC | 9097 |
rs374334237 | snp | A/G | 0.000127711 | 0.00798995 | intron-variant | USP14 | GRCh38.p7 | 18:199366 | GAATTCCATGTTTGC[A/G]AGTAAGCCAAAGTCA | 9097 |
rs374335394 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:210290 | TTCTGATAATACTTT[-/T]CGTAATGTGAACTTT | 9097 |
rs374361299 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:208303 | AATTGTTTCTAGTAT[G/T]TATTACCCTTTTGAT | 9097 |
rs374369626 | snp | A/C/T | 0.000115453 | 0.00759705 | synonymous-codon | USP14 | GRCh38.p7 | 18:211221 | TGGAGACTGGCATAT[A/C/T]GCTTACGTTCTACTC | 9097 |
rs374401278 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:207916 | AGAAATAAAATTAAC[G/T]TTGTATATGGATCTT | 9097 |
rs374425982 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:165104 | CAGGTCACCACCACC[A/G]TGCGTGACAAATGTT | 9097 |
rs374497001 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:207248 | TTGAAATTGTGAAGT[A/G]TCAGCCTTCACTTTT | 9097 |
rs374502685 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:187147 | TTTATTGGTGACTTA[C/T]ATTTCTAAGGTAAAA | 9097 |
rs374586575 | in-del | -/AGG | | | cds-indel | USP14 | GRCh38.p7 | 18:212506 | CTACTTGGGAGGCTG[-/AGG]TGGGAGAATTGCTTG | 9097 |
rs374612116 | in-del | -/TT | | | intron-variant | USP14 | GRCh38.p7 | 18:166768 | GTGGTTAAATGTCTT[-/TT]GTTTGTCTTTGAAAC | 9097 |
rs374617554 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:168205 | TGCTAGGATTACAGG[C/T]GTGAGCCACCGCACC | 9097 |
rs374675826 | snp | A/G | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212349 | CGGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT | 9097 |
rs374742892 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:164863 | TTTACTTCCTTTGGA[A/G]TGATCTCAGTGACCA | 9097 |
rs374747643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:180635 | CTACTTTCTGTCATA[A/G]ATTTGCTCATTCTGG | 9097 |
rs374905598 | snp | A/G/T | 0.000362823 | 0.0134644 | intron-variant | USP14 | GRCh38.p7 | 18:192825 | TCTATTGTTTAACTC[A/G/T]GCTTTAATGTTCCTA | 9097 |
rs374967434 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:190735 | TTTCTATATCATTAC[C/T]TTTTATTTATTGACT | 9097 |
rs374976489 | snp | C/T | 9.9397e-05 | 0.00704902 | intron-variant | USP14 | GRCh38.p7 | 18:197613 | TCTTTTTTTACATTA[C/T]AGGATGCTAATGAAT | 9097 |
rs374980775 | snp | C/T | 9.88452e-05 | 0.00702942 | synonymous-codon | USP14 | GRCh38.p7 | 18:196734 | TTTCCCACAGTTTGC[C/T]GAGAAAGGTGAACAA | 9097 |
rs375058482 | in-del | -/T/TGAT | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214013 | ATGATGATTGATTGA[-/T/TGAT]TGATTGATAGTAAAT | 9097 |
rs375058905 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:202373 | TGGTTAAGATATGTG[C/T]AGCAGCTAAAGGCTT | 9097 |
rs375166011 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:171433 | TAAATCTACTCTGCC[A/T]GTGCTCTGTATATGG | 9097 |
rs375192464 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:164284 | AATGTGGAACAATAC[A/C]GATAGGTTTGTTTTC | 9097 |
rs375219486 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:208480 | GTTTTTAGTTGTATT[G/T]ATTTCTGCTCTTATT | 9097 |
rs375312486 | in-del | -/GT | | | intron-variant | USP14 | GRCh38.p7 | 18:208380 | ATATTAGTAATTTGT[-/GT]TTGTCCCCCTTGCTT | 9097 |
rs375338291 | in-del | -/A | | | intron-variant | USP14 | GRCh38.p7 | 18:176159 | TGATTGTGTCCCCCC[-/A]AAAAAAAAAACATTT | 9097 |
rs375347298 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:180838 | TTCCTATTTTATGGC[C/T]GAATAGTATTTCATG | 9097 |
rs375503360 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:162403 | CCATTCTAATGGCTG[G/T]GAAGTGGGATTTCTA | 9097 |
rs375507532 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:159276 | GCTTCGTTTTCGTTT[C/T]ATCAAACGTTGCATT | 9097 |
rs375565080 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:160074 | TTGGGAGGCTCGAGG[C/T]GGGCGGATCACTTGA | 9097 |
rs375579543 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:184752 | CAGGCTGGGTAATAG[A/C]GTGAGGCCCTGTCTC | 9097 |
rs375607826 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:166553 | GGTCCGGCTGGTTTC[A/G]AACTCCTGACCGCAG | 9097 |
rs375626122 | snp | C/T | 0.000188451 | 0.00970516 | intron-variant | USP14 | GRCh38.p7 | 18:210077 | TTGTATGTGGGTCTT[C/T]TTAAGGTAAAATTTA | 9097 |
rs375665995 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:185917 | ATGTTGCTCAGGCTG[G/T]TTTCAAACTCCTGGC | 9097 |
rs375669299 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:193199 | GGGATAGCCAGCGAC[A/G]GGTTTTATCATAATC | 9097 |
rs375687529 | in-del | -/TAGT | 0.00597247 | 0.0543191 | intron-variant | USP14 | GRCh38.p7 | 18:188360 | GATACATTATGTTAA[-/TAGT]TAGCCTAATAGTAGA | 9097 |
rs375696289 | snp | C/T | 6.80203e-05 | 0.00583142 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:211303 | TCATTTTAGTATTTA[C/T]GCTTAGATGTGAAAA | 9097 |
rs375774554 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:172263 | AAAAGAATAGAAAAA[C/T]GGAGCTTGAAATTGT | 9097 |
rs375780307 | snp | A/G | 3.75305e-05 | 0.00433172 | intron-variant | USP14 | GRCh38.p7 | 18:179061 | CACCAGATTTTATGT[A/G]TTTGATCACTACTTT | 9097 |
rs375783363 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:201192 | CATTGCAACATCTAG[A/C]TATTTGAAGAAGGGC | 9097 |
rs375817682 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:204813 | TACTTTGTATAGTAT[A/T]ATTTGGATCAATCTG | 9097 |
rs375833718 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:179585 | ATGGTTTTTTTTTTT[G/T]CTTTTTTTTTTTTTT | 9097 |
rs375936917 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | USP14 | GRCh38.p7 | 18:166752 | TTCAGCTTGTACAGT[A/G]GTGGTTAAATGTCTT | 9097 |
rs375941123 | snp | A/G | 1.68627e-05 | 0.00290363 | intron-variant | USP14 | GRCh38.p7 | 18:210357 | GTCTATTCATTGTCT[A/G]ATATTAATGGATTTA | 9097 |
rs375962364 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:161100 | GCCTAGCTCATTTTT[A/G]TATTTTTAGTAGAAA | 9097 |
rs376044972 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:172972 | ATTTTATCTAAGTCA[A/G]TTGATCACATTTTTT | 9097 |
rs376080751 | in-del | -/TG | | | intron-variant | USP14 | GRCh38.p7 | 18:201385 | ATAAACACTGAAGTG[-/TG]GGACATGGATTATGT | 9097 |
rs376098488 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:209122 | TTTTGATGTTTTGCC[C/T]TTTTTTTTTTGTCTT | 9097 |
rs376160033 | in-del | -/AT | 0.0126979 | 0.078662 | intron-variant | USP14 | GRCh38.p7 | 18:190322 | ATGCATATGCACAAA[-/AT]ATATATGAGTGAAAC | 9097 |
rs376171317 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:192337 | GGGAGGCCGATGTGG[G/T]TGGATCACCTGAGGT | 9097 |
rs376235145 | snp | A/G | 1.65165e-05 | 0.00287367 | missense | USP14 | GRCh38.p7 | 18:197673 | CAGAAATTGGAAGCA[A/G]TAGAGGATGATTCTG | 9097 |
rs376319542 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:195381 | TTTGTGCTAAGATGC[A/T]GTATTTGGTGGGTTC | 9097 |
rs376338969 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP14 | GRCh38.p7 | 18:191913 | ACTGAATGATAATTT[C/T]TGAGCTTTTGTAATA | 9097 |
rs376341840 | snp | A/T | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:211490 | ATTGTGCTGCCCTAT[A/T]TAAAGGTGGCAGAAA | 9097 |
rs376360682 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:165042 | CAACCACCGCCTCCC[A/G]GGCTCAAGTGACTGT | 9097 |
rs376368916 | in-del | -/A | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214003 | AGATAGATAGATGAT[-/A]GATTGATTGATGATT | 9097 |
rs376408423 | in-del | -/GTTA | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214120 | ACAGTTAGTTAGTTA[-/GTTA]TGAGTGAGCACAGCT | 9097 |
rs376419661 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:169293 | TTGACTTTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 9097 |
rs376467867 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:187246 | TGTATTATTATTAAA[C/T]ATTTTTGAGACCTGT | 9097 |
rs376490355 | snp | C/G/T | 9.98725e-05 | 0.00706593 | intron-variant | USP14 | GRCh38.p7 | 18:180380 | AGGGATGTTCACATT[C/G/T]GGATGAGTAGTATTG | 9097 |
rs376508639 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:169791 | TTTTGGTGATTCTTG[C/G]AATATTTGAAACATT | 9097 |
rs376567022 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:209648 | AACACTGGGGAATTG[G/T]GTTTTTCCTTTTCTG | 9097 |
rs376844459 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP14 | GRCh38.p7 | 18:194230 | TTTTACTCTAACTTT[C/T]TTTCCTAAAGTAGAC | 9097 |
rs376876055 | snp | A/G/T | 0.0134861 | 0.0810011 | intron-variant | USP14 | GRCh38.p7 | 18:173391 | GCTGGGATTACAGGC[A/G/T]TGAGCCACCATGCCC | 9097 |
rs376876311 | snp | A/G/T | 6.59395e-05 | 0.00574161 | synonymous-codon | USP14 | GRCh38.p7 | 18:192884 | GGAAATGGCTTCAGC[A/G/T]CAGTATATTACTGCA | 9097 |
rs376953585 | snp | A/T | 4.95356e-05 | 0.00497648 | intron-variant | USP14 | GRCh38.p7 | 18:198139 | TGAAACTACGTATCC[A/T]TATGAGCCAAGATAT | 9097 |
rs376978163 | snp | C/T | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:211996 | ACAAGCTCTGGTTGC[C/T]TATTTTTAGAAAATG | 9097 |
rs377084272 | snp | A/T | 4.95421e-05 | 0.00497681 | synonymous-codon | USP14 | GRCh38.p7 | 18:204641 | AATGGTGTCTTTTCG[A/T]TCCAAATTCAAGGAT | 9097 |
rs377096951 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:168720 | AATTACAGGCGTGAG[A/C]CACTGTGCCAGGCCT | 9097 |
rs377182250 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:190274 | CATTTTTGGGCACAT[C/G]CATTTGTTTCTGTTG | 9097 |
rs377184479 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:165348 | TAGAGATAAAGACAG[A/G]CTACCCCCACTGGGC | 9097 |
rs377194713 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP14 | GRCh38.p7 | 18:209076 | TTTACATTTAGTGCA[A/G]TCATCGACATGTTAG | 9097 |
rs377200179 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:202714 | AGTATCTAAAAGTCT[C/T]CCCATATTGTCATCA | 9097 |
rs377205009 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:185283 | TCTGTCTCAGCCTCC[C/T]AAGTAGCTGGAATTA | 9097 |
rs377226294 | snp | A/G | 8.67265e-05 | 0.00658451 | intron-variant | USP14 | GRCh38.p7 | 18:199171 | ACAAATTGAATACCC[A/G]TTGGCATATTCCTTA | 9097 |
rs377289947 | multinucleotide-polymorphism | CCC/TCT | | | intron-variant | USP14 | GRCh38.p7 | 18:158915 | CAGGGGAGCGCCGTC[CCC/TCT]CTGAGCCACCGATGG | 9097 |
rs377293190 | snp | A/G | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:213973 | TGGACAAGATAGATA[A/G]ATTAGATAGATAGAT | 9097 |
rs377410575 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:165198 | TGATATGCCTGCCTC[A/G]GGCCTCCCAAAGTGC | 9097 |
rs377540276 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:161069 | AGTAGCTGGAATTAC[A/G]GGCGCCTGCCACCAT | 9097 |
rs377542849 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:185330 | TGCCTGACTAATTTT[-/T]GTATTTTTAGTAGAG | 9097 |
rs377614300 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:162206 | CTGCTGTAAACATGG[A/G]TGTACAAATATCTGT | 9097 |
rs377722249 | snp | A/G | 1.70104e-05 | 0.00291632 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:211304 | CATTTTAGTATTTAT[A/G]CTTAGATGTGAAAAT | 9097 |
rs377749564 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | USP14 | GRCh38.p7 | 18:192810 | TAGAATGAATTGAAT[C/T]CTATTGTTTAACTCG | 9097 |
rs386800088 | multinucleotide-polymorphism | AGT/GGC | | | intron-variant | USP14 | GRCh38.p7 | 18:174649 | AGGTCTTGCTTTGTC[AGT/GGC]TGGAGTGCAGTGGCA | 9097 |
rs386800089 | in-del | CCTG/GAGGTCAAGA | | | intron-variant | USP14 | GRCh38.p7 | 18:189725 | TGACCTCGTGATCCA[CCTG/GAGGTCAAGA]CCTCGGCCTCCCAAG | 9097 |
rs386800090 | in-del | CA/T | | | intron-variant | USP14 | GRCh38.p7 | 18:199940 | CGTGACTAACAAAAT[CA/T]ACTGTATAGTCAGAA | 9097 |
rs397828035 | in-del | -/GTA | | | intron-variant | USP14 | GRCh38.p7 | 18:195384 | TGCTAAGATGCTGTA[-/GTA]TTTGGTGGGTTCAGT | 9097 |
rs397858256 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:177648 | TTTTTTTTTTTTTTT[-/T]AAATCTCCACTTCTG | 9097 |
rs397858894 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:174284 | CTTTTTTTTTTTTTT[-/T]TGAGACAGTCTTGCT | 9097 |
rs397972792 | in-del | -/TAGATAGAT | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:213971 | ATGGACAAGATAGAT[-/TAGATAGAT]AGATTAGATAGATAG | 9097 |
rs398031810 | in-del | -/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:174285 | TTTTTTTTTTTTTTT[-/T]GAGACAGTCTTGCTC | 9097 |
rs527256980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:164682 | TGGTCTTGAACTCCT[A/G]ACCTCAAGTGATCTG | 9097 |
rs527291233 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:205864 | AATTCTCTGGCGACT[C/T]ATCCAGGGTGTTGTG | 9097 |
rs527344448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:206385 | TCTTGTCTTTTCCCT[A/G]TTTTCTAATTGTACT | 9097 |
rs527345762 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, downstream-variant-500B | USP14, LOC105371951 | GRCh38.p7 | 18:158541 | GTGTTGCTGCGTCAT[C/T]GCCAGTGGCCGGTTT | 9097 |
rs527359992 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:198378 | TAGCTGGGATTACAG[G/T]TGCATGCCACCATAC | 9097 |
rs527560399 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213153 | CTTGTAACTTTGCAA[A/C]GTCTTTTTTATTCAT | 9097 |
rs527582413 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:163990 | TTACTAGGGAACTAG[C/G]AGGTAATGATCTCCA | 9097 |
rs527638247 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:185418 | CCTCAGCCTCCCAAA[G/T]TGCTGGGATTACAGG | 9097 |
rs527661698 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:177269 | TGTCTTTGGAAAAAG[A/C]TTCTTGGCCTGGTGG | 9097 |
rs527665220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:171612 | AGACATAAACGAGAT[A/G]AATGTTGTTTTCCTG | 9097 |
rs527698501 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | USP14 | GRCh38.p7 | 18:173353 | CCTGACCTCGTGATC[A/C]GCCCGCCTTGGCCTC | 9097 |
rs527785836 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:179544 | TTTAACACCTAGCAT[G/T]TATTTAGTGCCATTC | 9097 |
rs527866274 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:192557 | GCGACAAGAGCAAAA[C/T]TCTGTCTCAGAAAAT | 9097 |
rs528006607 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:204165 | TTGAACTATATCACT[A/G]TTACTTCTATGTAAA | 9097 |
rs528082243 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:188017 | TTTACTTCATGTTTC[C/T]TTCGTGCTTCACTGG | 9097 |
rs528154662 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:204005 | TACATCTCCATAGAG[A/T]CCTGGGAGGGGCCTA | 9097 |
rs528206436 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:161015 | TCACTGCGACCTCCA[C/T]CTCCTGGTTTCAAGC | 9097 |
rs528261230 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:195946 | GATTGCTTTGTAAGG[A/T]CTTCTGGTGAGTTAA | 9097 |
rs528385871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:189221 | TTAGATTTGTTCATT[C/T]AATTTTTTGAGTTGT | 9097 |
rs528487613 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:190355 | GCTGGGTCATAAAAG[G/T]ATTTATATATTCAGT | 9097 |
rs528536865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:182925 | CAGAAATCTTGAAGT[C/T]GTTTTTAAGAAGTGT | 9097 |
rs528591192 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:183697 | TCTTAATTTTTGGAT[A/C]TAAATCCTGCTTTTA | 9097 |
rs528660380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:162564 | ATGTGCTTTATTCTC[C/T]CAGGAATTTTTCTTC | 9097 |
rs528687109 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:203907 | AGTTAAATCACTGGT[G/T]CCCAAAGAGTACTTA | 9097 |
rs528769078 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:202127 | TTTTCTTAAAGCAGA[C/G]CACATAAGTAGTGCT | 9097 |
rs528799989 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:159368 | GGGTGTCATTTCTTG[A/G]TTGGCGTTTGACAGG | 9097 |
rs528813803 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:172431 | GATTTAAAATATTAC[A/G]TAGGCTTACTTGATA | 9097 |
rs528887391 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:193309 | AGGATAGAAATAACT[G/T]GTTTCTTCATTGCAT | 9097 |
rs528887710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:201044 | CTGACCTTGTGATCC[A/G]CCCACCTCGGCCTCC | 9097 |
rs528935295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:185697 | ATTTAAAAAAATTTT[A/G]AATTATTTTTTATTT | 9097 |
rs528968267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:193951 | GGTATGCATCTAGGA[A/G]TGGAGTTAATTACTG | 9097 |
rs529019624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:186700 | GAGGCTGCAGTGAGC[C/T]GAGATTGCACCACTG | 9097 |
rs529083775 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:206771 | CTGGGTATGGTGGTG[C/T]GGACCTATAATCCCA | 9097 |
rs529085119 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:172099 | TAAAATTAGTTGGGC[A/T]TGGTGGTGTATACCT | 9097 |
rs529085197 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP14 | GRCh38.p7 | 18:165376 | GGCAGTAAAACACAC[A/G]TTGGAGGAAAATCTT | 9097 |
rs529154231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:207883 | CATTGTCTAGAGTGG[C/T]TAGTAAAGCTAGCAT | 9097 |
rs529263338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:173295 | TTGTATTTTTTTTAG[C/T]AGAGACGGGGTTTCA | 9097 |
rs529293555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:209125 | TGATGTTTTGCCTTT[C/T]TTTTTTTGTCTTCTT | 9097 |
rs529377993 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:195111 | TCTTATTAGTCTCTT[C/T]TAATCTATATTTCTT | 9097 |
rs529379667 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:161799 | AAACAATATATATCC[G/T]TGGGTTTTAAAAATA | 9097 |
rs529409250 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:200072 | TGGGTGTTCCTGCTT[C/T]ACACTGTGAAGAAGC | 9097 |
rs529487475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:178690 | TTACAGAGTTGTGCA[A/G]CCTTCACCACAGTCT | 9097 |
rs529627040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:169970 | TTCTCGAGCCTCCCT[A/G]TTCCCTGAGACAAGA | 9097 |
rs529670614 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:207703 | AAAGTATTAAGTCTT[A/G]CAATCCATAAACTTC | 9097 |
rs529716925 | in-del | -/T | 0.00755907 | 0.0610114 | intron-variant | USP14 | GRCh38.p7 | 18:172389 | CTAGTGAAGAAGCTG[-/T]TGAATGTTGTTGAAA | 9097 |
rs529768778 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157838 | TGTGACACAGAGACA[A/C]GAAGTGAGCACATGC | 9097 |
rs529778110 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | USP14 | GRCh38.p7 | 18:213808 | TTGCTGTGTATAGGG[G/T]GTGTTCACATATATC | 9097 |
rs529848317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:182838 | GCAGGAGACTGCAAC[A/G]TACTCAGTGCAACTG | 9097 |
rs529899395 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:174477 | CACCATGTTGGTCAG[C/G]CTGGTCTCAAACTCC | 9097 |
rs529960302 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:169568 | CTGGGATGTGCAGTT[C/G]TCAAATTTCTTGGTT | 9097 |
rs529961832 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:183607 | AGTTCTGTCTTACAT[G/T]TTACTGATTCATACG | 9097 |
rs530062016 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:198911 | GAAACAATTTATGTA[C/T]CTTTGGGCTTCTAAG | 9097 |
rs530087271 | in-del | -/TGTT | 0.00571424 | 0.0531457 | intron-variant | USP14 | GRCh38.p7 | 18:178005 | AAATAATTTTATTAG[-/TGTT]TGTTTGTTTGTTTGT | 9097 |
rs530171245 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | USP14 | GRCh38.p7 | 18:186045 | CAACTTGTTCTTGAC[-/A]AAAAAAATTTTAAAT | 9097 |
rs530171598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:176627 | GCCCCTAGTTTATTG[C/T]TTTCAAATGTTTTAT | 9097 |
rs530194062 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:189091 | AAGAGTTATTCTACT[A/G]TTGGACCTGTATGGT | 9097 |
rs530220063 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:156616 | ATAATCTTATTTAGT[C/T]CTTATAACAATCCTG | 9097 |
rs530239295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:171553 | ATTCCTTTCAAAATA[C/T]TACTGCTTATTGACA | 9097 |
rs530239827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:198281 | TCGCTCTTGTCGCCC[A/G]GGCTGGATTGCAATG | 9097 |
rs530264675 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:180169 | ATTTTAGTGATTTAT[A/G]TATGCCATGTCATTT | 9097 |
rs530267678 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, downstream-variant-500B | USP14, LOC105371951 | GRCh38.p7 | 18:158491 | CCGCCCAGTCTCCTC[C/G]CTGCAGTCGCTCCGG | 9097 |
rs530311325 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:183511 | TATTAAAATTTCTAG[A/T]TCTGTTTTTTAGTCT | 9097 |
rs530362695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:184440 | TTAGCAGAACTTGTC[C/T]TTGGCAGGTTCTATA | 9097 |
rs530424424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:188578 | TATGTCTATCTTTTC[C/T]TGGAACTTTTATTTT | 9097 |
rs530437433 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:209913 | TTGAACACTTACAGA[G/T]AATTCAAATTTTATT | 9097 |
rs530442807 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:175886 | TTGGAGTTTTCTTTG[C/T]AGGAAGACTTTAAGA | 9097 |
rs530455275 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP14 | GRCh38.p7 | 18:190938 | GAATTTTTTTTTGGA[C/T]ATTAAATTACATATG | 9097 |
rs530456738 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:159514 | GGTGTCTCCAATTGG[C/T]TGTAGGTGTGTGATT | 9097 |
rs530575821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:161117 | ATTTTTAGTAGAAAC[A/G]AGGTTTCACCGTATT | 9097 |
rs530576981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:180450 | TTAATTTATTATACA[A/G]TTCAGCATTTTAAAG | 9097 |
rs530626569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:201962 | CTTTGCTGCTGAATA[A/G]ACTTGGTTAAATGTT | 9097 |
rs530643070 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:173404 | GCTTGAGCCACCATG[A/C]CCGGCCTATATTGTC | 9097 |
rs530749995 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP14 | GRCh38.p7 | 18:195923 | CTCAGAAGTTGTTTA[C/T]AGCTAGTGATTGCTT | 9097 |
rs530803600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:194884 | TACAGTGAGCTGAGA[C/T]TGTGTCAGTGTACTC | 9097 |
rs530872573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:187739 | GAGTACTAATTTCAA[A/G]TATCAGATTTCCATG | 9097 |
rs530889952 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP14 | GRCh38.p7 | 18:194400 | ATGAAAAATACTGTT[C/G]TTTACATTTTTGCTT | 9097 |
rs530934293 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:196455 | CTTGAACCCAGAAGG[C/T]GGAGGTTGCGGTGAG | 9097 |
rs530940610 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:190096 | TGATGTTTAGTGTAT[C/T]CATGTTCTGTGTATT | 9097 |
rs531093945 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:210832 | TCTCCTGTTAGTGTT[C/T]GCATTCAGTCTGTTG | 9097 |
rs531107994 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:173632 | GTCTCCATGTTGGTC[A/T]GGCTGGTCTTGAACT | 9097 |
rs531118264 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:162463 | TGGATTTTTTCTTAA[C/T]TGAGCACCTCTTGTT | 9097 |
rs531181374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:162031 | CACTTTAGGTATCTC[A/G]TATAACCAGAATCAT | 9097 |
rs531251365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:159726 | CTCTTGAAATATTCT[A/G]ATACTTAAACACACC | 9097 |
rs531281064 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:192622 | TTGACAAAGGGAAAG[A/G]GCTTAAAGTAGGCTC | 9097 |
rs531404076 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:187755 | TATCAGATTTCCATG[A/G]TTCCAAGATATACTT | 9097 |
rs531408960 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:200093 | GTGAAGAAGCACCTA[G/T]TGCTTTGTGCTGTAC | 9097 |
rs531428163 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214199 | CAAACCATCATTTGT[G/T]GATCCTCTGCTTGAA | 9097 |
rs531471568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:193195 | TCTGGGGATAGCCAG[C/T]GACGGGTTTTATCAT | 9097 |
rs531570290 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:168843 | TTTGGGAGGCCGAGG[C/T]GGGTGGATCACGAAG | 9097 |
rs531576590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:171499 | AGTATGGAGTACTGA[A/G]TATTTTAAGGCCACC | 9097 |
rs531579918 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:173038 | GTGCCAAGTTTACAA[G/T]ATTTTTTTTTTCTGT | 9097 |
rs531622834 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:206004 | GTTTGTCTGTGATGA[A/G]TAAACCTGCTGTAAA | 9097 |
rs531631499 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | USP14 | GRCh38.p7 | 18:173144 | GACGGAGTCTCACCC[A/T]GTTGCCCAGGCTGGA | 9097 |
rs531641963 | in-del | -/AGA | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157324 | CAGCATTTTACCCAC[-/AGA]AGAACTTTCAAATTT | 9097 |
rs531686216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:206609 | GTCATATCTAAGAAA[A/G]CATTGCCGGGCTCGG | 9097 |
rs531718186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:167304 | GAGTCTTGAAATAAG[A/G]TAGTATATGTTCTTA | 9097 |
rs531736610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:201276 | AACCATGACCAATAA[A/G]GAGAAGTCTTGAAGG | 9097 |
rs531751198 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:204090 | AGCGTTGTATGAGAA[A/G]GTTAAATGTAGTTGA | 9097 |
rs531775906 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:166720 | GTACATTAAAATAAA[A/T]TGATTATTAGATTGT | 9097 |
rs531904351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:178555 | GTAACCACTACCACA[A/G]TCACGATTTAGAAGT | 9097 |
rs531928868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:185668 | AGCTTTTTGAGGGCA[C/T]GTCTTCATTTAAAAT | 9097 |
rs531990396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:174403 | CCTGAGTAACTGGGA[C/T]TATAGGCACTTGCCA | 9097 |
rs532062991 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212030 | ACATTTAATAATAAT[A/T]AAAAAAAAGGGATTA | 9097 |
rs532065887 | in-del | -/TT | 0.00318978 | 0.0398085 | intron-variant | USP14 | GRCh38.p7 | 18:197892 | TATTATTTATTAAAC[-/TT]AATTCATTGTTGATT | 9097 |
rs532121885 | snp | C/T | 0.000412694 | 0.0143589 | intron-variant | USP14 | GRCh38.p7 | 18:204714 | TCTTACTGCTGACTT[C/T]ATACTCTTAATATCT | 9097 |
rs532123901 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212974 | ATCTGTGAACACTAG[A/G]AGGGGATAAAATAAG | 9097 |
rs532164776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:189304 | TAGGCTTGTTTTATT[A/G]TCTATTTTCTAACTT | 9097 |
rs532237732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:169932 | TCTGACAGCCTCACC[A/G]ACCCGCAGTTCCCTC | 9097 |
rs532291554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:182594 | ACCTACAGTCTAATA[A/G]AGAAAGACTATCAAG | 9097 |
rs532523682 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:199871 | TTCCCCTAGGAGCAG[C/T]GGTTCAGTATTCATT | 9097 |
rs532532508 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:173040 | GCCAAGTTTACAAGA[-/T]TTTTTTTTTCTGTTT | 9097 |
rs532535951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:191783 | TTGCCGATATTGGGT[A/G]ATACTAGTTTTTTTT | 9097 |
rs532545972 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:183904 | TCTGAATAGGTAGTT[C/T]GCTGGGGTAGCTTTC | 9097 |
rs532579616 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:205302 | CTTTTATACTTATCT[C/G]CTCAAAGTACTTCAC | 9097 |
rs532583622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:191113 | AGTGATGTTCAGGGT[A/G]TGTCTGCTATATTAG | 9097 |
rs532591768 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:168397 | AATATTCGTGACTTT[A/C]AGATTTCTTAAACTT | 9097 |
rs532610272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:175360 | CCTGACCTTAGGGGA[A/G]AAGCCTCCAGTCATG | 9097 |
rs532674462 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP14 | GRCh38.p7 | 18:176161 | GATTGTGTCCCCCCA[A/G]AAAAAAAACATTTGG | 9097 |
rs532707061 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:163769 | TGTCACAGGGTTTCA[A/G]TGTACGGATTTCATC | 9097 |
rs532753073 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:197156 | ACCTTTCAAGTGCCC[G/T]CTTCCTGCAGGGCCT | 9097 |
rs532779581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:194659 | ATCTGGGCTGGGTGC[A/G]GTGGCTCATGCTTGT | 9097 |
rs532828170 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:165755 | AAGTGATCTTAGGGG[A/G/T]CATTTATAGTTATCA | 9097 |
rs532865284 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:193624 | GCCCTACCCATTTAT[C/T]TATGTGTTATTTCTC | 9097 |
rs532876283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:198241 | GAAAAATTCTTCAGA[A/G]GTTTTTTTTCTTTGA | 9097 |
rs532878991 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:184328 | TATGTCTTTGGAAAA[A/G]TGGCACTAACTGATA | 9097 |
rs532951293 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:191246 | CAGGCATTATTGTGA[A/C]TTATTGTGTATTGAA | 9097 |
rs532961136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:208603 | CATTCTGTTCCTTGT[A/G]TTTTTAAAAATTTAT | 9097 |
rs532985026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:200510 | GCTTTTGGCAGAGCC[A/G]GAACTAGAACTTGCT | 9097 |
rs533010534 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:187619 | ATGGATTTTTTTCAC[A/G]TGTTTTATTTCCAAC | 9097 |
rs533077309 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:179610 | TTTTTTTCCTTGAGA[G/T]GGGGTCTTGCTCTGT | 9097 |
rs533120629 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:159890 | AACTCAAGTAGATTT[C/G]TAAGGTCCCTTCCTT | 9097 |
rs533124760 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:166619 | ATTACAGGCGTGAGC[C/T]ACTGTGCCTGGCCAA | 9097 |
rs533220145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:201072 | TCCCAAAGTGCTGGG[A/G]TTATAGGAATGAGCC | 9097 |
rs533246116 | in-del | -/A | | | intron-variant | USP14 | GRCh38.p7 | 18:166328 | GTACCACTTGTGTTT[-/A]AAAAAAATTTTTGTT | 9097 |
rs533283869 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:194102 | GTACTTAGTATTGTA[G/T]GTCTTTTTGACTATA | 9097 |
rs533284745 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:188743 | AGTGCAGTGGCATGA[A/T]CTCGGCTCACTGCAA | 9097 |
rs533292432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:196369 | TAAAAAAAAAAATAC[A/G]AAAAATTAGCCGGGA | 9097 |
rs533354267 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:169210 | AGCCTGGCCAACATG[A/G]TGAAACCCCGTCTCT | 9097 |
rs533439247 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:196038 | ACTTAAAAATGTTTA[A/C]GCAGCTGGGTGTGGT | 9097 |
rs533461174 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:168065 | GCCTGAGCTGGGATT[A/T]CAGGCGCCCACCACC | 9097 |
rs533510928 | in-del | -/CC | | | intron-variant | USP14 | GRCh38.p7 | 18:200920 | ATTCTCCTGCCTTAG[-/CC]CCTCCTGAGTAGCTG | 9097 |
rs533546214 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:190752 | TTTATTTATTGACTT[C/G]ACAGAGATAAGGAAA | 9097 |
rs533553795 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:195035 | TGTCCATTAAAAAAG[-/T]TTTTTTTTTTTCCTT | 9097 |
rs533617592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:167529 | GGTTTTTTTTTTGAG[A/G]CAGGGTCTCACTCTC | 9097 |
rs533752113 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:179143 | GAAGACTTAATCATT[A/C]ATACCAAGATAGATA | 9097 |
rs533777333 | snp | C/G | 8.24124e-05 | 0.00641868 | missense | USP14 | GRCh38.p7 | 18:163404 | TGTTTGCGTTGACTG[C/G]AGTCCAGCCTGCCAG | 9097 |
rs533794054 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:178059 | GGGTCTCCCTCTGTC[A/G]CGCAGGCTGGAATGC | 9097 |
rs533822090 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:204824 | GTATTATTTGGATCA[A/G]TCTGTATTACAATTA | 9097 |
rs533924627 | snp | C/T | 6.59707e-05 | 0.00574291 | synonymous-codon | USP14 | GRCh38.p7 | 18:211218 | TGGTGGAGACTGGCA[C/T]ATCGCTTACGTTCTA | 9097 |
rs533962879 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:206112 | GCATGGTAGTTGCAT[G/T]TTTAGTTTTTCAGGA | 9097 |
rs534287138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:206859 | TGAGCTGAGATCACG[C/T]CACTGCCCTCCAGTC | 9097 |
rs534351067 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:199610 | CCCCCCAAGCACAGG[G/T]CTGAGTGCTGTCTAG | 9097 |
rs534502371 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP14 | GRCh38.p7 | 18:187901 | GATTATGATTTATGA[C/T]ATATTTATGAGGAAA | 9097 |
rs534524637 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:171209 | ATGAAGGTAGCTACA[C/G]TATACAACAGATTTT | 9097 |
rs534625985 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:173322 | TTCACCATGTTAGCC[A/G]GGATGGTCTCTATCT | 9097 |
rs534642019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:168233 | ACCCGGCCAAAATAC[A/G]GTTGATTTTTCTAAG | 9097 |
rs534692555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:202541 | AGAGTGAATATTCTG[A/G]TAATAAACAGGAATG | 9097 |
rs534730907 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:181118 | TTTCATTTTATGGAT[A/G]TATCACATTTTATTT | 9097 |
rs534807715 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:169149 | TAATCCCAGCACTTT[G/T]GGAGGCCAAGGATGG | 9097 |
rs535056743 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:193062 | TACTTATTTTATCGT[A/C]CAGATTATAAATCAA | 9097 |
rs535116814 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:205658 | TGGTGGCATACACCG[A/G]TAGTTCTAGCTACTT | 9097 |
rs535132847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:174569 | CTGCACCCGGCTTAT[C/T]TCATGGTTTTTAATG | 9097 |
rs535187839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:171779 | TCTGGAAAGGATTCA[C/T]CTGAATTCTTGATAC | 9097 |
rs535231400 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:196194 | CCAGGCATGGTGGCA[G/T]GCTCCTGTAATCCCA | 9097 |
rs535298613 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:196478 | GCGGTGAGCCGAGAT[C/T]GCGCCACTGCACTCC | 9097 |
rs535320189 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:163811 | AAGCATAGTACCCGA[C/T]AGGTAGTTTTTTTTT | 9097 |
rs535359007 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:180827 | GTAACACCTCATTCC[C/T]ATTTTATGGCTGAAT | 9097 |
rs535365487 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:170762 | TAACACAGGAACAGA[A/G]AACCGAACACCGCAT | 9097 |
rs535379975 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:161145 | ATTGGCCAGGCTGGT[C/T]TCAAACCCCTGACCT | 9097 |
rs535410004 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:184614 | CAAACAAACAAAAAA[A/C]CAAAAATTAGCCAGG | 9097 |
rs535457489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:193643 | GTGTTATTTCTCTCT[A/G]GATTTGCCTACTCTG | 9097 |
rs535486598 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:176860 | ATACAGTTTTTCTCA[A/G]TATTTTTCATTGTAT | 9097 |
rs535487361 | snp | C/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:201447 | GCTCTCATCTATAGT[C/T]TGGGATAAGGTTGGC | 9097 |
rs535535588 | in-del | -/T | 0.0858192 | 0.188533 | intron-variant | USP14 | GRCh38.p7 | 18:179587 | GGTTTTTTTTTTTGC[-/T]TTTTTTTTTTTTTTC | 9097 |
rs535579466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:187289 | TAACTGGGTTTATTT[A/G]TTGAGGTCTGATTTT | 9097 |
rs535595842 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:169263 | GAGTGTCATGGTGCA[C/T]GCCAAGAGAATTGCT | 9097 |
rs535605929 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:173643 | GGTCAGGCTGGTCTT[C/G]AACTCCTGACCTCAG | 9097 |
rs535626748 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:158782 | CGCGTAGGCCTGGCC[A/T]GCACGGGCGGGCACC | 9097 |
rs535630005 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:165648 | AATGAGTGTCAAAGA[C/G]GTTTAAGTAACATAG | 9097 |
rs535715897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:192020 | TGTAAATTAAGTGAG[A/G]ATCATAAAGCTGAAA | 9097 |
rs535770632 | in-del | -/GT | | | intron-variant | USP14 | GRCh38.p7 | 18:180085 | GGGGGAAATAAAACT[-/GT]TTCTTTAGCGTGAAG | 9097 |
rs535777887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:192689 | CATATTTCTGGTCAT[A/G]CAAGACCAGAAGAGA | 9097 |
rs535814026 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:208766 | TATTTATTTATTTGA[A/G]ACTGAGTCTTGCTCT | 9097 |
rs535830313 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:173520 | AGGTTCAAGAGATTC[G/T]CCTGCCTCAGCCTCC | 9097 |
rs535847532 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:196582 | AATTAATTTACAGTC[A/G]CGTGTATTAAATATG | 9097 |
rs535991935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:190559 | TTTCACTATGGGTAA[A/G]GATTGTGGCCTACAT | 9097 |
rs536038812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:168368 | AATAATGACAATTTT[A/G]CTTCTCCCTTTTCAA | 9097 |
rs536038851 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:173740 | TTATCTGTTTTGAGT[A/T]AATTCTTGTGTTTGC | 9097 |
rs536093004 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:195397 | GTATTTGGTGGGTTC[A/G]GTCTGTATAATGATG | 9097 |
rs536124217 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:208343 | GTGTTTAGTGAGTGA[C/G]ATCCATCCCGTTTCA | 9097 |
rs536136877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:211130 | CTTGTCCCTGTTATT[C/T]AGATGAATGGATTAA | 9097 |
rs536171417 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | USP14 | GRCh38.p7 | 18:160145 | CTGTCTCTACTAAAA[A/C]TACAAAAAATCAGTC | 9097 |
rs536260304 | snp | A/C/G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:206816 | TGAGGCAGGAGAATC[A/C/G/T]CTTGAACTGGGGAGG | 9097 |
rs536273374 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157107 | AAAAAATGCTAAGGA[C/T]CATCTGAGCTATCAG | 9097 |
rs536283168 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:195359 | GAACATTTTATTGAG[C/T]CCCTGCTTTGTGCTA | 9097 |
rs536290052 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:173195 | CTCACTGCAAGCTCC[A/G]CCTCCTGGTTCACGC | 9097 |
rs536314401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:195198 | TATACTAGATCTTAA[A/G]TCATCTGTTTTTTTG | 9097 |
rs536328982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:205549 | GAATCTGAGGCAGGA[A/G]GATCACTTTAGGCCA | 9097 |
rs536391628 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:175600 | TATATATTGCTAGAT[G/T]CTATTTGCTTATCTT | 9097 |
rs536434146 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:183419 | TTTAGTCTGAGGACT[C/G]TTGTCGCAAACTCTA | 9097 |
rs536592425 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212191 | ATCTTCTTTGCCTGC[C/T]TGTATTTTAAAAAGA | 9097 |
rs536645717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:170289 | AGCCTGGCCAACAGA[A/G]CGAGACTCTGTCTCA | 9097 |
rs536706719 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:171095 | TCACGAGGTTTAAAG[A/G]AAGAAGCAATCTCTG | 9097 |
rs536768615 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:167547 | GGGTCTCACTCTCAC[A/G]TATGCCGGAGCACAG | 9097 |
rs536793874 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:206034 | ACATTCGTGTACAGG[C/T]TTTAATGTAAACGTA | 9097 |
rs536860903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:194160 | TCATTGTTGTCAACC[A/G]TTGATTTTTGATATT | 9097 |
rs536861512 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:161834 | TTTCAAAAGTTAGCT[A/G]TTTTATGAGGCTGAT | 9097 |
rs536898105 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP14 | GRCh38.p7 | 18:174886 | GTTCAAGCAGTTCTC[A/G]TGCCTCAGCCTCCCG | 9097 |
rs536921071 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:186969 | GAGTTAGTGGGTTAA[G/T]AAATTAGAGTGGATA | 9097 |
rs536923692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:184000 | CTGTTTTCTTCTTGG[A/G]TGCCTTTTAGCCTCT | 9097 |
rs536934837 | snp | A/T | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:211728 | CTTATCTAACAAACA[A/T]TTTTCCAGGAAGGTG | 9097 |
rs537099518 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:161728 | ATTTCAGGAGTTGGA[A/C]AGCAATTAACAGTTG | 9097 |
rs537109157 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:167056 | CACTAGTACCAAATG[C/G]TTTTGATTACTAAAG | 9097 |
rs537130141 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:208866 | TTCTCATGCCTCAGC[A/G]TCCCGAGTAGCTGGG | 9097 |
rs537152532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:160880 | TTATGACAGCCTTTC[A/G]GGAATTACACATTGC | 9097 |
rs537183887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:173551 | TGAGTAGCTGGGATT[A/G]AAGGCATGCACCACC | 9097 |
rs537205141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:209404 | AAGTTATTTTTCTCA[C/T]GTTGCATGCTAAAAT | 9097 |
rs537317375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:178160 | AAGTAGCTGGGACTA[C/T]AGGCATGCACCCCTA | 9097 |
rs537379339 | snp | A/T | 1.79661e-05 | 0.00299712 | intron-variant | USP14 | GRCh38.p7 | 18:178920 | TTCATGAAATTACTT[A/T]TTTTAAAAACAGGGA | 9097 |
rs537460521 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:184177 | TTTTCGCTTTTTGGT[G/T]TTTATTTTTAGTATT | 9097 |
rs537465181 | snp | C/T | 3.30825e-05 | 0.00406696 | missense | USP14 | GRCh38.p7 | 18:198066 | ACTCCTCATCTGCAT[C/T]GGCAGCGACACCTTC | 9097 |
rs537493092 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:191806 | TTTTTTTTAAATTTT[G/T]ATTTTAGTCACTCTA | 9097 |
rs537517119 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP14 | GRCh38.p7 | 18:184564 | TTTGAGACTAGCCTC[A/G]GCAACGTGGCAAAAC | 9097 |
rs537517827 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:167237 | CAGTGAGCCGAGATC[C/G]TGCCACTGCACTCCA | 9097 |
rs537582069 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:176312 | AAACCCAGGCAAATG[A/G]TGGTGACTTTTTTGG | 9097 |
rs537642089 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157359 | ATTTCTTTCAAAATT[A/G]GAGTCAATCCTGTCA | 9097 |
rs537661867 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:202312 | AGAGGGATAAATACC[A/G]TTTCCACTGTTACAC | 9097 |
rs537680814 | snp | A/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157968 | ATATAAATATATAAA[A/T]ATATATAAATATATA | 9097 |
rs537723708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:195503 | CATGAAGGAGGGCAA[A/G]GTATGATCACTAGGA | 9097 |
rs537749099 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:178008 | TAATTTTATTAGTGT[G/T]TGTTTGTTTGTTTGT | 9097 |
rs537767738 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, downstream-variant-500B | USP14, LOC105371951 | GRCh38.p7 | 18:158627 | CCGCCGCAGCTGCTC[C/T]TGGTCCCCGTCCCTT | 9097 |
rs537795531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:191536 | GTATAGAACATTTCT[A/G]TCATCTCAGAAAATT | 9097 |
rs537936750 | snp | A/G | 4.96635e-05 | 0.0049829 | intron-variant | USP14 | GRCh38.p7 | 18:192937 | CTTTTTGATAGGAGT[A/G]AGACATTCTATTTTT | 9097 |
rs537998145 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:204970 | GTCTCAACCTCCCAG[A/G]CGCAAATGATCCTCC | 9097 |
rs538027536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:164135 | TTTACAGTTATCTGT[A/G]TTGTGTGAATTTTTT | 9097 |
rs538050387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:171249 | TGAAGCAGCCTGATA[C/T]TGGAAAAAGATGCTG | 9097 |
rs538155342 | in-del | -/T | 0.00755907 | 0.0610114 | intron-variant | USP14 | GRCh38.p7 | 18:189995 | AATCTCATAGATCAA[-/T]TTTTACCAGTTTTGA | 9097 |
rs538188235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:198552 | AAAAAATACAATAAT[A/G]GAAATTAGGAATTTG | 9097 |
rs538206350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:210292 | TCTGATAATACTTTC[A/G]TAATGTGAACTTTAG | 9097 |
rs538234297 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:159439 | CAGGGATCACTTTTA[C/G]TTAGGGAATGGACCT | 9097 |
rs538331012 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:203972 | AATCTGACTGTTTTT[G/T]TTGAGTTGTAGTTCT | 9097 |
rs538380867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:193562 | AACATTATCATTCCA[A/G]AAAGCAACTTCATAA | 9097 |
rs538405345 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:196506 | TCCAGCCTGGGCAAC[A/G]GACCAAGACTCCATC | 9097 |
rs538414092 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:185818 | CCTGACTTGGCTTCC[C/T]GAGCAGCTGGGACCT | 9097 |
rs538416155 | in-del | -/GTG | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:176798 | TAATTAATTGTTGTT[-/GTG]GTATGGTATGAAGTA | 9097 |
rs538443148 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:180696 | GTGGCCTTTTTGCGG[C/G]TAACTTCTTTCATTT | 9097 |
rs538462830 | in-del | -/AGTT | 0.223835 | 0.248627 | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214111 | GAGCCATAGACAGTT[-/AGTT]AGTTAGTTATGAGTG | 9097 |
rs538511735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:173511 | CCGTCTCCCAGGTTC[A/G]AGAGATTCTCCTGCC | 9097 |
rs538551806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:165553 | TTTATTGAGTACTTA[C/T]TTTATGTCAGGCTTT | 9097 |
rs538574924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:168309 | CAGTTGTGTTTTGGG[C/T]AGATTCCATTGGGTT | 9097 |
rs538620303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:162165 | CACTTGAGTTGCTCC[C/T]ACTTTTTCGGCTGTT | 9097 |
rs538679543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:162674 | ACACATGGGGGCTGC[A/G]AAACTTATCATTTTG | 9097 |
rs538695067 | in-del | -/TC | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212074 | TCAAGTCTTTTGTCT[-/TC]TGAGTGTTGGAGCTT | 9097 |
rs538753426 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:173724 | CACCGCACCCGGTCT[A/G]TTATCTGTTTTGAGT | 9097 |
rs538776565 | snp | C/T | 0.000118478 | 0.00769579 | intron-variant | USP14 | GRCh38.p7 | 18:163502 | ATTATTGTATACTTT[C/T]TGAAAAATAACGCCA | 9097 |
rs538800250 | in-del | -/AAAG | 0.00119737 | 0.0244387 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213400 | AAAAAGCATTATTCC[-/AAAG]AAAGAATTTTTTCAA | 9097 |
rs538822868 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:173343 | GTCTCTATCTCCTGA[C/T]CTCGTGATCAGCCCG | 9097 |
rs538871394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:189628 | GCTGGGACTACAGGC[A/G]CGTGTCACAACGCCC | 9097 |
rs538925051 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:176685 | TTACATCAATTGTTA[A/C]TATTTATGTCAGTTT | 9097 |
rs538987055 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:166954 | ATACTTACCTTTTCC[C/T]ATTGACTTGTGTTGG | 9097 |
rs539131431 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212574 | ACACCACTGCACTCC[A/T]GCCTGGGTGACAGAG | 9097 |
rs539154999 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | USP14 | GRCh38.p7 | 18:202622 | ATTTGGGGCATAGCT[-/A]AAAAAGAGCAAACAG | 9097 |
rs539164555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:166457 | CTTGTCTCAGCCTCC[C/T]GAGTAGCTGGAATTA | 9097 |
rs539236797 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:159765 | CACACACATAAAACA[A/G]AACCCCTCTGTTTCC | 9097 |
rs539275823 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157735 | GGTGGTTAGTGGCAC[A/C]CCAAAACAACTAAAA | 9097 |
rs539292128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:190403 | ACCAGTTTCAAAAAC[A/G]GAGGTACCAATTCAT | 9097 |
rs539320040 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:193488 | TTTAAAGTGTATAAT[G/T]CATTGTTTTTTAGTT | 9097 |
rs539409941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:178089 | CAAGTGGTGTGATCA[C/T]AGCTCACCACAGCCT | 9097 |
rs539426537 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:191790 | ATTGGGTGATACTAG[-/T]TTTTTTTTAAATTTT | 9097 |
rs539475779 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:172694 | AAGATCATTAACTGA[A/T]GGCTTAGATGATTGT | 9097 |
rs539519930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:188030 | TCTTTCGTGCTTCAC[C/T]GGCTAGAACTTTTAA | 9097 |
rs539563000 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:194821 | CTGTAATCCCAGCTA[C/T]TCGGGAGGCTGAGGC | 9097 |
rs539579145 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:179983 | CTGCAAAAAAGGCAA[G/T]ACTAGTATGATTATT | 9097 |
rs539677429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:160816 | TCAAGCCTGATTTCT[C/T]TGCTGCTGCAAGTGA | 9097 |
rs539772458 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:185948 | CTCAATCAATCCTCC[C/G]AGCTCAGTCTGCCAA | 9097 |
rs539794220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:202121 | TGTTTGTTTTCTTAA[A/G]GCAGAGCACATAAGT | 9097 |
rs539868896 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:166914 | TCATGTGTATATCCA[G/T]TTGTTCCAGCACTAT | 9097 |
rs539915835 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:174388 | CTCCTTCCTCAGCCT[C/G]CTGAGTAACTGGGAT | 9097 |
rs539923356 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:169418 | TCTAGTTCACTACAA[C/T]TTAAAATTATGAAAG | 9097 |
rs539995378 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:192314 | CATGCCTGTAATCCC[A/G]GCACTTTGGGAGGCC | 9097 |
rs540014739 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:203764 | ACAGGCGCCCGCCAC[C/T]GTGCCCGGCTAATTT | 9097 |
rs540062973 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:208837 | TGCAACCTCTGCCTC[C/T]TGGGTTCAAGCAATT | 9097 |
rs540359444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:169412 | TCTTATTCTAGTTCA[C/T]TACAACTTAAAATTA | 9097 |
rs540460626 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212893 | GCTCGGCAGAGCACA[A/C]CACTGATGATAACTA | 9097 |
rs540575906 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:183164 | TTATCCTTGGATGAT[A/C]ATATTGCTTGGAGCA | 9097 |
rs540584068 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:205646 | ATCAGTTGGATGTGG[C/T]GGCATACACCGGTAG | 9097 |
rs540620812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:208934 | TATTTTTATTAGACA[C/T]AGGGTTTCATCATGT | 9097 |
rs540627279 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, downstream-variant-500B | USP14, LOC105371951 | GRCh38.p7 | 18:158316 | ACCACGTGGCCAGTG[C/T]GCGCAGGGCGATGGG | 9097 |
rs540644182 | snp | C/G/T | 0.000396868 | 0.0140812 | intron-variant | USP14 | GRCh38.p7 | 18:198174 | TATACTCATACCTTA[C/G/T]TAGAATTGGCATAAA | 9097 |
rs540667324 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:160989 | CTGGAGTGCAATGGC[A/G]CGATGTTGGCTCACT | 9097 |
rs540775584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:184292 | ACTAACGTAATTGAT[A/G]CAAGATGTCATGGAT | 9097 |
rs540832158 | in-del | -/A | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:207515 | AAACCCTGTCTCCAC[-/A]AAAAAATACAGAAAT | 9097 |
rs541001257 | snp | G/T | 0.000808832 | 0.0200938 | intron-variant | USP14 | GRCh38.p7 | 18:197731 | GATTATAGACTTTCG[G/T]TATACCTTGATTTTT | 9097 |
rs541106305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:194525 | CTCATTTTTCCGTTA[C/T]GCATGTAATTTTTTT | 9097 |
rs541143000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:162398 | AATAGCCATTCTAAT[A/G]GCTGTGAAGTGGGAT | 9097 |
rs541165808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:195666 | TAGCTGTCCAGTAGA[A/G]TCAGCTGTTTAAGGA | 9097 |
rs541167648 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:187547 | ATATTTAGCTTCCCC[A/C]TCCAGGAATATAGGC | 9097 |
rs541216865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:172880 | TGCTTTCTCATGCTC[C/T]GGAACCCAAACTGTA | 9097 |
rs541272717 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:209744 | TTGGTCATCACATTC[A/T]GGGTGTCTGTTACTG | 9097 |
rs541280272 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:166612 | TGCTGGGATTACAGG[A/C]GTGAGCCACTGTGCC | 9097 |
rs541330022 | snp | A/G | 0.000132293 | 0.00813196 | synonymous-codon | USP14 | GRCh38.p7 | 18:180253 | GGAGTTACCATGTGG[A/G]TTGACAAACCTTGGT | 9097 |
rs541350926 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:167236 | GCAGTGAGCCGAGAT[C/G]GTGCCACTGCACTCC | 9097 |
rs541409044 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:173563 | ATTAAAGGCATGCAC[C/T]ACCACACCCAGCTAA | 9097 |
rs541411199 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:186857 | CAATTCAAACAGTCT[C/T]AAATTTGTGCTCATG | 9097 |
rs541413450 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:164539 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 9097 |
rs541414758 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:170712 | ATTCTGTGAAGGCTG[A/G]GAGAGGTGAGGAAGC | 9097 |
rs541476153 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:164643 | ATTTTTAGTAGAGAT[G/T]GGGTTTCACCATGTT | 9097 |
rs541499098 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:183374 | AGACTGTGGGTTTTA[C/T]TTATCTTATAAAAGT | 9097 |
rs541537033 | snp | A/G | 0.000133267 | 0.00816184 | intron-variant | USP14 | GRCh38.p7 | 18:210501 | GAAACAAGGTAAAGG[A/G]TATTCTTTTTTCAAC | 9097 |
rs541537989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:165142 | TTGGTAGAGACAGTG[C/T]TTCACCATGTTGGCG | 9097 |
rs541584779 | snp | C/T | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212284 | GATTCTTTCCTTGGC[C/T]CAGTTGTGTTTGTAT | 9097 |
rs541644858 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:188407 | ACATTCGTATTCTTT[A/C]AATATATAGCGCTGA | 9097 |
rs541727318 | in-del | -/CAAA | 0.00119737 | 0.0244387 | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:213938 | TTCTTTTAAAGTTGG[-/CAAA]CAAACATTTTCTGTA | 9097 |
rs541779931 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:190537 | CATATGTTATAAATG[A/T]ACTTTATTTCACTAT | 9097 |
rs541921922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:186448 | GCAATGCAATGAGAC[C/T]CTGCCTCTTAAAAAA | 9097 |
rs542070503 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:184229 | ACCTCTGATGCCAAA[C/G]AAAAGAAGTAGTTTT | 9097 |
rs542094163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:199973 | TCAAACAAACTTCAA[C/T]TAGCTCTTCATTTCA | 9097 |
rs542094171 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:192492 | ATTGCTTGAACCCAG[C/G]AGGTAGAGGTTGCAG | 9097 |
rs542104117 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:165329 | AAAGATCTATAGTTA[A/T]CTTTAGAGATAAAGA | 9097 |
rs542154883 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:193030 | AGTGTACATTATACT[A/T]AAGTTAAACAACTTG | 9097 |
rs542213274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:185458 | CTGTGCCTGGCTGAA[A/G]ATATTTGTCTGTTAA | 9097 |
rs542262042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:189075 | TAAATTATTTCAGCT[C/T]AAGAGTTATTCTACT | 9097 |
rs542275952 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:177208 | ATTGTGTTTTCCAAC[G/T]GGTTATTGCTAGTGT | 9097 |
rs542323127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:181296 | GATTTTCCAAAGTGA[C/T]GGTACCATTTTACAT | 9097 |
rs542393325 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:175761 | TCTGAGTTTGTATTA[A/G]TATTTTTTCTTCCTT | 9097 |
rs542400968 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:181370 | GATTAAGCCATCTAG[C/T]GCTATGAAGTGTGGT | 9097 |
rs542413029 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:209581 | GCAGGAATTCTTGTT[G/T]TAGAGGTAGTTGTTT | 9097 |
rs542430429 | snp | G/T | 3.45042e-05 | 0.00415342 | intron-variant | USP14 | GRCh38.p7 | 18:202847 | TAAAATTTTTAAAAC[G/T]AATGTTTGGTCTTCT | 9097 |
rs542431596 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:198632 | TATGTTTTGATTAAT[A/G]TAATTATTTTAAATT | 9097 |
rs542491931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:203754 | AGCTGGGACTACAGG[C/T]GCCCGCCACCGTGCC | 9097 |
rs542492530 | in-del | -/TC | 0.00279162 | 0.0372561 | intron-variant | USP14 | GRCh38.p7 | 18:162601 | AAACTATCTAACCTT[-/TC]TCTCTCTCTCTCTTC | 9097 |
rs542557027 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:196311 | CATGAGGTCAGGAGT[C/T]GGAGACCAGAGCCTG | 9097 |
rs542655037 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:156768 | ATAAAAGTTATGTTT[C/T]TACTATACTGTAGTC | 9097 |
rs542674621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:189639 | AGGCGCGTGTCACAA[C/T]GCCCAGCTAGTTTTT | 9097 |
rs542771920 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:173646 | CAGGCTGGTCTTGAA[A/C]TCCTGACCTCAGGTG | 9097 |
rs542813584 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:170890 | GAGCATCAGGATAAA[C/T]AGCTAATGCATGCTG | 9097 |
rs542819879 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:196228 | ACTCGGGAGGCCCTT[C/T]TGTGTTCAAGCAGTT | 9097 |
rs542824105 | snp | A/C | 0.000842968 | 0.0205128 | stop-gained | USP14 | GRCh38.p7 | 18:210411 | CAATAATTGTGGATA[A/C]TATGACTTACAAGCA | 9097 |
rs542942875 | snp | C/G | 0.00636936 | 0.0560724 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:211722 | CTTTGCCTTATCTAA[C/G]AAACATTTTTCCAGG | 9097 |
rs542960980 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212701 | ATATGAGGTATTTCA[A/C]TATGATAGGCTTCTT | 9097 |
rs542965335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:163077 | CACCACGCCCAGCCT[A/G]CTGAAGTCTCAGTTT | 9097 |
rs542983372 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:163624 | TTAGAGTAAGGGAGA[A/C]ATATTGTAGCTGTTT | 9097 |
rs543071234 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157485 | AGTTTCCATCTCAAG[A/G]AACCACTTTCTTTGC | 9097 |
rs543124762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:197563 | TATTTTGGAAGAACT[C/T]TGTAGATCATTCACT | 9097 |
rs543376479 | in-del | -/TGTTGTTGAAT | 0.00755907 | 0.0610114 | intron-variant | USP14 | GRCh38.p7 | 18:172385 | ACTCCTAGTGAAGAA[-/TGTTGTTGAAT]GCTGTGAATGTTGTT | 9097 |
rs543461133 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:208507 | TATTTCCTTTATTCT[C/G]CTTGCCTTGTGATAT | 9097 |
rs543477248 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:199742 | ATGTTAATTAATCAA[C/T]ACAATATGTGAAATA | 9097 |
rs543483427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:173357 | ACCTCGTGATCAGCC[C/T]GCCTTGGCCTCCCAA | 9097 |
rs543544927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:193939 | TCATTTCTCTTTGGT[A/G]TGCATCTAGGAGTGG | 9097 |
rs543584949 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:201520 | AGTCACGCTCTGTCT[A/T]ATGATACCGAGGGGA | 9097 |
rs543604409 | in-del | -/T | 0.434976 | 0.168179 | intron-variant | USP14 | GRCh38.p7 | 18:185861 | ACTATGCCCAGCTGA[-/T]TTTTTTTTTTTTTTT | 9097 |
rs543659346 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:194499 | TACTAACTTTTAGTC[A/G]CATTTGGTTTCTCAT | 9097 |
rs543663159 | in-del | -/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157536 | CTTGCCCATTAAAGC[-/T]TTGTCTTGAGATTGC | 9097 |
rs543689561 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:176836 | CTGATAGTATGTTTT[G/T]TCTAAAGTATACAGT | 9097 |
rs543716057 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:172045 | TGGGAGTTTGAGACC[A/T]GCCTGGGCAACACAG | 9097 |
rs543723360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:187403 | TTGATCCATATTTTA[C/T]ATATCTTTGAACTTC | 9097 |
rs543774922 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:172820 | AACATGATGTTTGTA[G/T]GCACTGGGGGAAAAT | 9097 |
rs543841347 | in-del | -/CTT | 0.0103295 | 0.0711199 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213679 | ACTCACTCAGTAGCC[-/CTT]CTTCTTCAGGATTAA | 9097 |
rs543882093 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:190980 | TTACAAAAAAAAGGT[A/T]GATAATTCATTAGTA | 9097 |
rs543933102 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:161120 | TTTAGTAGAAACGAG[G/T]TTTCACCGTATTGGC | 9097 |
rs543966015 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212987 | AGGAGGGGATAAAAT[A/G]AGCATTGCAGGGAAA | 9097 |
rs544011014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:163770 | GTCACAGGGTTTCAA[C/T]GTACGGATTTCATCA | 9097 |
rs544016883 | in-del | -/C | 0.00636936 | 0.0560724 | intron-variant | USP14 | GRCh38.p7 | 18:161573 | TCTAGCCTCCTCCCA[-/C]CCCCCCCATTAGGCT | 9097 |
rs544036493 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:196957 | TTGCCCCTTTGCAGT[G/T]TCTCTACACAGCCCG | 9097 |
rs544106958 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213041 | CCTAAACTTTGACTT[C/G]GCAATCAATACTTTC | 9097 |
rs544127690 | in-del | -/TGA | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214010 | TAGATGATGATTGAT[-/TGA]TGATGATTGATAGTA | 9097 |
rs544238180 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | USP14 | GRCh38.p7 | 18:191799 | ATACTAGTTTTTTTT[A/T]AATTTTGATTTTAGT | 9097 |
rs544330229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:170410 | ACAGAAAGCTAGAAA[C/T]GATTAAGCTTAGTAA | 9097 |
rs544413942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:197493 | AGATCGTATGTCTTA[C/T]TTGGCTTAATATTTT | 9097 |
rs544483544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:198260 | TTTTTTCTTTGAGAC[A/G]GAGTTTCGCTCTTGT | 9097 |
rs544592520 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:167804 | TAACAGGTGTGAGTC[A/G]CTGTGCCCAGCCCTT | 9097 |
rs544663264 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:176069 | TAGTGCTGCTTTTTC[A/G]TTTTCCTCTCTAGTA | 9097 |
rs544698789 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:195773 | ACCCGCTATCCTGAT[C/G]TTGGCAGAGTAGCAG | 9097 |
rs544748265 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | USP14 | GRCh38.p7 | 18:213777 | GTACTGTCTTCTGCT[A/G]CTACTACTTAGTGCT | 9097 |
rs544871508 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:167278 | AGAGCGAGACTCCGT[C/G]TCCAAAAAAAGAGTC | 9097 |
rs544885264 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | USP14, LOC105371951 | GRCh38.p7 | 18:158380 | ATGGGGCCCCGCGCC[C/T]GTCCCTCACTTGCTC | 9097 |
rs544900008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:209522 | TTCAGTTCATTTGTG[C/T]TGGCGTGGTAAGTGG | 9097 |
rs544925230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:158898 | GTCGGAGCCCTGCGT[A/G]GCAGGGGAGCGCCGT | 9097 |
rs544946479 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:194750 | AGCCTGGCCAACATG[A/G]CGAAACCCCGTCTCT | 9097 |
rs544953300 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:182870 | CTGGAGAAGGATGGA[G/T]GTAGAAACGGTGATA | 9097 |
rs545173605 | snp | A/G | 1.65127e-05 | 0.00287334 | missense | USP14 | GRCh38.p7 | 18:180338 | AAAGATGCCCTTAAA[A/G]GGTAAGACTGCAGTC | 9097 |
rs545224931 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:195711 | TCCAGGAGTTGAGTA[G/T]ATGAGAACCAACTAT | 9097 |
rs545284841 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:201900 | TTTAAGATATTTTAT[A/C]TTTTGTTCTGATAAT | 9097 |
rs545286246 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:183437 | GTCGCAAACTCTAGG[A/C]CATTTCTTGGTCATT | 9097 |
rs545292000 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:161049 | TCTCCTGCCTCAGTC[G/T]CGCGAGTAGCTGGAA | 9097 |
rs545300293 | in-del | -/A | | | intron-variant | USP14 | GRCh38.p7 | 18:198777 | AATAACTTTTAAAAT[-/A]AAAAAAGAATTTTTT | 9097 |
rs545341640 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:161605 | TAAGTTTATGGAGAG[G/T]CTTCCCAATGCTTTG | 9097 |
rs545346509 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:173575 | CACCACCACACCCAG[C/G]TAATTGTTTGTATTT | 9097 |
rs545381265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:169219 | AACATGGTGAAACCC[C/T]GTCTCTATTAAAAAT | 9097 |
rs545389284 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:165250 | CCACACCCGGCCTCT[A/G]TTATTTTTAATAATA | 9097 |
rs545410251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:168570 | CTCCTGAGTAGTTGG[A/G]ATTACAAACGCCTAC | 9097 |
rs545442770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:163052 | AAGTACTGGGATTAC[A/G]GGCGTGAGCCACCAC | 9097 |
rs545450273 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:203778 | CCGTGCCCGGCTAAT[A/T]TTTTTGTATTTTTAG | 9097 |
rs545465281 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:209421 | TTGCATGCTAAAATG[A/T]GTTGAAGCAGTGAGT | 9097 |
rs545500686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:159608 | TGATACGAATCAAGA[A/G]TATTGTTTGATCTCA | 9097 |
rs545513200 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:204498 | GCATTACTTCAGATA[C/T]GTGATACTTTAAATA | 9097 |
rs545787357 | in-del | -/TTT | 0.00284473 | 0.0376068 | intron-variant | USP14 | GRCh38.p7 | 18:180212 | TTAATGATTTAATCC[-/TTT]TTTTTTTTTTTTTCC | 9097 |
rs545848113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:206485 | ATTTTCTCCTAGTCT[A/G]TAGCTTATGTTTTCA | 9097 |
rs546049003 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:176419 | TAGCCTTCCGACTAC[C/G]TTGGACTACAGGTGT | 9097 |
rs546105555 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:200889 | TCACTGCAACCTCTG[A/C]CTCCCAGGTTCAAGA | 9097 |
rs546166746 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:193748 | CAGGATTCATCCACA[C/T]TATGGCATGTATCAG | 9097 |
rs546226392 | in-del | -/T | 0.311723 | 0.243173 | intron-variant | USP14 | GRCh38.p7 | 18:197742 | TCGTTATACCTTGAT[-/T]TTTTTTTTTTATTTT | 9097 |
rs546298282 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:210968 | ACCTGGTGGAACCCC[G/T]GCAGTGCCCTTAAGC | 9097 |
rs546340501 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:200054 | ATCTCACTTTTTAAT[C/G]ACTGGGTGTTCCTGC | 9097 |
rs546349357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:195955 | GTAAGGTCTTCTGGT[A/G]AGTTAAGATTTAAAA | 9097 |
rs546351203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:188016 | GTTTACTTCATGTTT[C/T]TTTCGTGCTTCACTG | 9097 |
rs546359677 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:163648 | GCTGTTTGACAACAC[C/T]ATATGGTATTATAAA | 9097 |
rs546374260 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:162047 | TATAACCAGAATCAT[C/T]CATGTTGCAGCATGT | 9097 |
rs546412633 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:188709 | TTGAGACAGAGTCTC[A/G]CTGTGTTGCCCAGGC | 9097 |
rs546462536 | in-del | -/C | | | intron-variant | USP14 | GRCh38.p7 | 18:190389 | AGTATGTTTTGCCAA[-/C]CAGTTTCAAAAACGG | 9097 |
rs546486384 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:189491 | TTTGTTTTTTCTTTG[-/T]TTTTTTTTTTGAGAA | 9097 |
rs546501068 | in-del | -/A | | | intron-variant | USP14 | GRCh38.p7 | 18:186751 | GGGAGACTGTGTCTC[-/A]AAAAAAAAAAGAGAA | 9097 |
rs546512894 | in-del | -/AGTTAGTT | 0.00137709 | 0.026204 | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214107 | GCTGGAGCCATAGAC[-/AGTTAGTT]AGTTAGTTATGAGTG | 9097 |
rs546626032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:168238 | GCCAAAATACAGTTG[A/G]TTTTTCTAAGTTTAT | 9097 |
rs546688990 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:168749 | CTTGTCCTACTTTTT[A/C]ATAGGACTTCTAATA | 9097 |
rs546749841 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:162623 | TCTCTCTTCTTTTCC[A/T]ATGCTGTGTGCTGAT | 9097 |
rs546759451 | snp | C/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:174580 | TTATTTCATGGTTTT[C/T]AATGTTGTCGTAAGT | 9097 |
rs546773402 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:196972 | TTCTCTACACAGCCC[A/G]CAATGTCCTTTTTAA | 9097 |
rs546920081 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:181606 | CAAATCTTTTCTTCT[A/G]TACTATAAGCTGTCA | 9097 |
rs546977109 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:190357 | TGGGTCATAAAAGGA[G/T]TTATATATTCAGTTT | 9097 |
rs547097664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:183853 | TGCTCATATCATGCA[A/G]CCATATTCTCTTCCT | 9097 |
rs547115446 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:175262 | TTTGTGCATTTTGTT[G/T]CTCTTTTTTTCTTTA | 9097 |
rs547208115 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:163153 | ATTCAGCACCTACTG[C/T]ATGCATGCTCCTCTT | 9097 |
rs547256591 | in-del | -/T | 0.00597247 | 0.0543191 | intron-variant | USP14 | GRCh38.p7 | 18:161854 | TGAGGCTGATTGAAA[-/T]TTTTTTATTGTGGTA | 9097 |
rs547346803 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:159864 | TCTTTTCCTCATCCC[A/C]CAAATGAAGGAACTC | 9097 |
rs547437412 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:185796 | ACCTCTTGGGCTCAA[A/G]GATCCTCCTGACTTG | 9097 |
rs547452642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:178030 | TTTGTTTGTTTGTTA[C/T]ATTTTTTGAGACGGG | 9097 |
rs547509254 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:202025 | TATGATTAGTAATTT[A/T]AAAAAATCAGACTTT | 9097 |
rs547531871 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:173354 | CTGACCTCGTGATCA[A/G]CCCGCCTTGGCCTCC | 9097 |
rs547544159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:206782 | GGTGCGGACCTATAA[C/T]CCCAGCTACTTGGGA | 9097 |
rs547633084 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:204012 | CCATAGAGTCCTGGG[A/T]GGGGCCTATCTATCA | 9097 |
rs547646545 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:199572 | TTTCTGCTTTTTGTT[C/G]GTTATTTCACTGTTT | 9097 |
rs547678688 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:173147 | GGAGTCTCACCCTGT[C/T]GCCCAGGCTGGAGTG | 9097 |
rs547699188 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157211 | GCTAAAGTTTGGGGT[A/G]GCTGTGGCAATTTCT | 9097 |
rs547728211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:160766 | ACTATTGTAATATGC[C/T]TCTAGTTTATTTTAG | 9097 |
rs547768002 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:173433 | TCTGTTTTTTTGAGA[C/T]GGAGTTCCGTTCTTG | 9097 |
rs547964673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:205855 | ACTCAGCATAATTCT[C/T]TGGCGACTCATCCAG | 9097 |
rs548063351 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:207147 | ATGAGTGTATTTCTA[A/G]ACTATTAATTTTATT | 9097 |
rs548105201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:169981 | CCCTATTCCCTGAGA[C/T]AAGACAGTATTGAAA | 9097 |
rs548108414 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:211019 | ACTTGGAGGACTGTT[A/G]GTGTGGCCAGTGGAG | 9097 |
rs548158550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:163847 | TAGATCCTCTTCCTC[C/T]TCCCACTCTCCACCC | 9097 |
rs548199793 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212228 | AAGTTGTAAAAGTAA[C/T]GGATTTCTTTGGATG | 9097 |
rs548217832 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157127 | TGAGCTATCAGTGAA[A/T]CATCATCTTTTTGCT | 9097 |
rs548280524 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:161016 | CACTGCGACCTCCAC[A/C]TCCTGGTTTCAAGCG | 9097 |
rs548327681 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:198318 | TCTTGACTCACTGCA[A/G]CCTCCACCTCCTGGG | 9097 |
rs548588854 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:168934 | ACAAAACAATTAGCC[A/G]TGCATGGTGGCAGGT | 9097 |
rs548589364 | snp | C/T | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214121 | CAGTTAGTTAGTTAG[C/T]TATGAGTGAGCACAG | 9097 |
rs548632917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:203776 | CACCGTGCCCGGCTA[A/G]TTTTTTTGTATTTTT | 9097 |
rs548643417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:185026 | TCATCCTAAAATTCT[A/G]TAAATTACTCCTCAA | 9097 |
rs548814958 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:184354 | TGATAAAACAAGAAT[C/G]AAAGAACAGAAAAAC | 9097 |
rs548965113 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:180480 | GTGTTTAATGCTTTT[G/T]ATAGTATTTACAAGT | 9097 |
rs549000890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:173314 | GACGGGGTTTCACCA[C/T]GTTAGCCAGGATGGT | 9097 |
rs549004539 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:194143 | AGGTATGAAGTGTTA[C/T]CTCATTGTTGTCAAC | 9097 |
rs549045527 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:179720 | AGGCTCCTGAGTAGC[A/G]AAAATTGTAGGCGTG | 9097 |
rs549122571 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:189512 | TTTTTGAGAAGGAGT[C/G]TCACTCTGCCTCCAG | 9097 |
rs549127520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:168145 | TGGTCAGGCTGGTCT[C/T]GAACTCCCGACCTCA | 9097 |
rs549259886 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:164020 | AGCTCCATCCATGTT[G/T]CTGTAAAGGACATGA | 9097 |
rs549294620 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:191729 | AGATCCATTCATATT[A/G]TTACTGACTAGATCA | 9097 |
rs549301140 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:188597 | AACTTTTATTTTCTT[C/T]CATGTTTTTATAGGA | 9097 |
rs549348396 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:196456 | TTGAACCCAGAAGGC[G/T]GAGGTTGCGGTGAGC | 9097 |
rs549412337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:197044 | TAGTGATTTTCTACC[A/G]CAGTCCTAAATCCTC | 9097 |
rs549433581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:190210 | TGAATATTTGGTTTA[C/T]GTTCAGTTTTTGGTG | 9097 |
rs549477551 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:176013 | AGTTGCTGAATTGAT[G/T]GTCATATTCTACTGT | 9097 |
rs549503728 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:176806 | TGTTGTTGTGGTATG[C/G]TATGAAGTAGAGAGC | 9097 |
rs549616081 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:158725 | CTCCGGTGAGCCCTG[G/T]CCTGGCCTCGCGCGC | 9097 |
rs549623541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:203507 | TGCACTACCCAGAAA[C/T]AGTGCCCTAGACCAC | 9097 |
rs549648133 | in-del | -/A | | | intron-variant | USP14 | GRCh38.p7 | 18:169077 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAGTGA | 9097 |
rs549649540 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:185685 | TCTTCATTTAAAATT[A/T]AAAAAAATTTTAAAT | 9097 |
rs549688704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:196137 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCTGTC | 9097 |
rs549766121 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:192645 | GTAGGCTCCATCTAA[A/G]TTCCCTTTTCAGCAT | 9097 |
rs549769322 | snp | G/T | | | missense | USP14 | GRCh38.p7 | 18:209973 | TTTTTCTCCTCAGAG[G/T]GACAAAAAGAGTAGT | 9097 |
rs549780874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:165356 | AAGACAGGCTACCCC[C/T]ACTGGGCAGTAAAAC | 9097 |
rs549851813 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:201333 | ACATTGGAATAGGTC[C/G]TCTGTGCAGAGGCCT | 9097 |
rs549853346 | snp | C/T | 0.00716266 | 0.059414 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:211706 | TCTGTAGCCACCCAT[C/T]CTTTGCCTTATCTAA | 9097 |
rs549890630 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:190143 | TCATGCTATATAGTA[C/T]AGTATTCCGTTGTGT | 9097 |
rs549895189 | snp | C/G | 4.95176e-05 | 0.00497558 | intron-variant | USP14 | GRCh38.p7 | 18:166774 | AAATGTCTTTTGTTT[C/G]TCTTTGAAACAGGAT | 9097 |
rs549921293 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:161279 | ATTTGATCCTTAGCC[A/G]GCTTCCAGTTTCATC | 9097 |
rs549924841 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:189444 | CAAAAGCCACTAGAA[A/G]GTCTCTTATCTTTTC | 9097 |
rs549981193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:160698 | TTCAGGTAGGTTCCT[C/T]TCCTTTACTTCTAGT | 9097 |
rs550087165 | in-del | -/A | | | intron-variant | USP14 | GRCh38.p7 | 18:177424 | AGTCCCTGTCTCTAA[-/A]AAAAAAAAAAAAAAA | 9097 |
rs550088136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:173080 | GCTTGATAAGTTTTA[A/G]CTGTTACATTTAGAT | 9097 |
rs550115220 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:208310 | TCTAGTATTTATTAC[C/T]CTTTTGATGTCTGTA | 9097 |
rs550135826 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:159983 | AGAGAACATTTTAAG[G/T]ACTATTTCATAAGAT | 9097 |
rs550186014 | in-del | -/ATT | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:199007 | ACACATTTATTACTC[-/ATT]GTTGTTTCTAGAATT | 9097 |
rs550190834 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212032 | ATTTAATAATAATAA[A/T]AAAAAAGGGATTAAT | 9097 |
rs550316486 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:162829 | TTGAGATGGAGTCTC[A/G]CACTGTCGCCCAGGC | 9097 |
rs550321297 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:180697 | TGGCCTTTTTGCGGC[C/T]AACTTCTTTCATTTG | 9097 |
rs550323535 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:188710 | TGAGACAGAGTCTCG[C/T]TGTGTTGCCCAGGCT | 9097 |
rs550339371 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | USP14 | GRCh38.p7 | 18:176160 | TGATTGTGTCCCCCC[A/C]AAAAAAAAACATTTG | 9097 |
rs550342909 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:162900 | CCTCCCGGGTTCAAG[C/T]GATTCTCCTGTCTCA | 9097 |
rs550362325 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:185297 | CCAAGTAGCTGGAAT[C/T]ACAGGTGTGTGCCAC | 9097 |
rs550384696 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:181620 | TATACTATAAGCTGT[A/C]ATTTTACTTTCTTTT | 9097 |
rs550427032 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:180461 | TACAATTCAGCATTT[C/T]AAAGTGTTTAATGCT | 9097 |
rs550476697 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:166225 | ACTTATGTGTTTTTT[A/C]GTATTTGATGCTGTA | 9097 |
rs550511820 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:174461 | AGTAGAGACGGGGTG[G/T]CACCATGTTGGTCAG | 9097 |
rs550623568 | snp | A/C | 6.22452e-05 | 0.00557842 | intron-variant | USP14 | GRCh38.p7 | 18:163286 | TATTTTTTAATTAAA[A/C]AAATTGTGATTTTGT | 9097 |
rs550629370 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:159590 | TTCAGCATTTACAAA[A/G]CATGATACGAATCAA | 9097 |
rs550651348 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:168887 | CCATCCTGGCTAACA[C/T]GGTGAAACTCCGTCT | 9097 |
rs550720210 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:184411 | GAGATGAGGAAGACC[A/T]TCCTCACAAATACTT | 9097 |
rs550910174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:190463 | TCTGTTCCACATCCA[C/T]CCCCAAGAGTTTAAG | 9097 |
rs550996698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:175405 | ATAGATGTTCATCAT[C/T]AGGTTCAGGAACTCT | 9097 |
rs550999081 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:194658 | AATCTGGGCTGGGTG[C/T]GGTGGCTCATGCTTG | 9097 |
rs551131207 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:208678 | GTAATTTTCCTGTTA[C/T]GTTTCTGTTGATTCT | 9097 |
rs551172914 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157717 | TTAGCTGTTTTACAC[G/T]GGGGTGGTTAGTGGC | 9097 |
rs551318697 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:201092 | AGGAATGAGCCACCG[C/T]GCCCAGCCAGGATTA | 9097 |
rs551336746 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:183910 | TAGGTAGTTTGCTGG[A/G]GTAGCTTTCTGGCTA | 9097 |
rs551416331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:187639 | TTATTTCCAACTGTT[C/T]TGAATTTTTGTATTT | 9097 |
rs551441861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:173190 | CTCGGCTCACTGCAA[A/G]CTCCACCTCCTGGTT | 9097 |
rs551511452 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:188105 | TGATTTTAATAGGAC[G/T]GTTGTATTTTAGGGT | 9097 |
rs551581387 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:188744 | GTGCAGTGGCATGAT[A/C]TCGGCTCACTGCAAC | 9097 |
rs551586017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:193503 | TCATTGTTTTTTAGT[C/T]TATCCACAGAGTTGT | 9097 |
rs551724768 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:173302 | TTTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 9097 |
rs551737217 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, downstream-variant-500B | USP14, LOC105371951 | GRCh38.p7 | 18:158560 | AGTGGCCGGTTTGAA[A/T]GAGACTCGTCGCACC | 9097 |
rs551885325 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:167515 | GTTTTGCATGAGTGG[-/T]TTTTTTTTTTGAGAC | 9097 |
rs551890966 | in-del | -/AAG | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213151 | GCTTGTAACTTTGCA[-/AAG]AAGTCTTTTTTATTC | 9097 |
rs552023147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:164059 | TAAAAGCATCATTTA[A/G]ATTTTATTTTAAAAT | 9097 |
rs552085818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:164702 | CAAGTGATCTGCCCA[C/T]CTTGGCCTCCCAGAG | 9097 |
rs552095302 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:202128 | TTTCTTAAAGCAGAG[A/C]ACATAAGTAGTGCTA | 9097 |
rs552109545 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:209828 | TTAACTGTGGTTATA[A/T]CATTTTAGTAATTTG | 9097 |
rs552174680 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:205950 | ACCACAATCTGCTTC[A/T]CCATTCACCTATTGA | 9097 |
rs552197610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:205455 | TGACAACTACCAACC[C/T]GTTCATTTCTATAAT | 9097 |
rs552250839 | in-del | -/TATTTTATTT | 0.00120144 | 0.0244801 | intron-variant | USP14 | GRCh38.p7 | 18:188670 | TCAGCTTTTTTGGGG[-/TATTTTATTT]TATTTTATTTTATTT | 9097 |
rs552314836 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:184495 | GTGATGGCTCACGCC[G/T]GTAATCCCAGTACTT | 9097 |
rs552351598 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | USP14 | GRCh38.p7 | 18:200653 | TTGCTTGCTGACTTA[A/C]TAATTTGGTGTGCTT | 9097 |
rs552372188 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:185100 | AAGCCCCAGCTCTCA[A/G]TATACACAGCGTTAA | 9097 |
rs552413172 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:191365 | ATTTAACACAATACT[C/G]TCTGTGATTTCTTTC | 9097 |
rs552435498 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:176697 | TTAATATTTATGTCA[C/G]TTTTAGAAAATCTTC | 9097 |
rs552445781 | snp | A/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213375 | AAAGCTTGATTTTTT[A/T]ATTTGATCTAAAAAA | 9097 |
rs552451867 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:192594 | TAAAATAAAATGTTC[A/G]TTTTATATGAGTTTG | 9097 |
rs552746169 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:159923 | ACCTCTCCATATTGA[C/G]AATCTGTATTTTGAG | 9097 |
rs552842736 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157839 | GTGACACAGAGACAC[A/G]AAGTGAGCACATGCT | 9097 |
rs552849639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:179251 | AGGGGTTTTTTTTTG[C/T]ATTGTACACCTTACT | 9097 |
rs552859424 | in-del | -/TGTT/TGTTTGTT | 0.274646 | 0.24944 | intron-variant | USP14 | GRCh38.p7 | 18:178008 | AATTTTATTAGTGTT[-/TGTT/TGTTTGTT]TGTTTGTTTGTTTGT | 9097 |
rs552879394 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:171624 | GATGAATGTTGTTTT[C/T]CTGTCTGCTACAACA | 9097 |
rs552882550 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:170217 | GCTGAGGCAGGAGAA[C/T]TGCTTGAGCCTGGGA | 9097 |
rs552913278 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:173257 | GGACTACAGGTGCCT[A/G]CCACCACACCCGGCT | 9097 |
rs553021970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:161520 | TGAAGCATTCCACTT[C/T]GTTGCTGTAGCCTTT | 9097 |
rs553040932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:203573 | GGAGATGGGTGTGAG[A/G]TAGGGAGTGATAACT | 9097 |
rs553054124 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:173565 | TAAAGGCATGCACCA[A/C]CACACCCAGCTAATT | 9097 |
rs553096840 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:162942 | AGCTGGGATTACAGG[C/T]GTGCGCCACCACACC | 9097 |
rs553153435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:179881 | GCTGGGATTACAGGT[A/G]TGAGCCACTGTGCCC | 9097 |
rs553192331 | snp | A/G/T | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:211985 | AGAAAATGTTGACAA[A/G/T]CTCTGGTTGCTTATT | 9097 |
rs553234884 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:167597 | TGCAGCTTTAAACTC[C/G]CAGCCTCAAGCAGTC | 9097 |
rs553351796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:174023 | CTTTTTTAAAGTTGC[A/G]TTGGCTATTCTGGGA | 9097 |
rs553433754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:171782 | GGAAAGGATTCACCT[A/G]AATTCTTGATACCAT | 9097 |
rs553463957 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:195051 | TTTTTTTTTTTCCTT[C/T]TTCAGGATTCAGTTT | 9097 |
rs553493252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:172568 | AAGGAAGTCAGTCAG[C/T]GTGGCAGGTTTCATT | 9097 |
rs553495191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:165699 | TGATTTATACATCAA[A/G]CAGATCTGTGTTCAC | 9097 |
rs553499986 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:167176 | CTGAGGCGGGAGGCA[C/G]AGGCAGGAGGCAGGA | 9097 |
rs553502683 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:196196 | AGGCATGGTGGCATG[A/C]TCCTGTAATCCCAGC | 9097 |
rs553508573 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP14 | GRCh38.p7 | 18:176905 | ATAATTTTTTAAGGG[A/C]ATTGTTTTAGTCTCT | 9097 |
rs553543016 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:178414 | CAATATTGTAAACAT[G/T]ATTAGGTGTTTTTAT | 9097 |
rs553591038 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | USP14 | GRCh38.p7 | 18:190403 | ACCAGTTTCAAAAAC[-/G]GAGGTACCAATTCAT | 9097 |
rs553635530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:188924 | CCTCAGGTGATCCCC[C/T]GGCTTTGGCCTCCCA | 9097 |
rs553703000 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:180942 | CGTTACAGCACACGT[A/G]ACACCTCATTCCTAT | 9097 |
rs553703058 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP14 | GRCh38.p7 | 18:189602 | ATTCTCCTACCACAG[C/T]CTCCTGAGTAGCTGG | 9097 |
rs553722932 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:194297 | GATCATTTATATCTA[A/C]TTCATTTGACAGCTC | 9097 |
rs553724725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:193664 | GCCTACTCTGGACTT[C/T]TACTCTAAATGGAAT | 9097 |
rs553785969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:194340 | ATAACTTAGAATTTC[A/G]GCAGCTTCTGCAGCA | 9097 |
rs553838156 | in-del | -/TT | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:180002 | AGTATGATTATTCTC[-/TT]ATTATATTTAAGAAG | 9097 |
rs553951478 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:166356 | GTTTTTTTTTGAGAT[G/T]GAGCCTTGTTCTGTT | 9097 |
rs554044582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:192021 | GTAAATTAAGTGAGG[A/G]TCATAAAGCTGAAAG | 9097 |
rs554067802 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:194551 | TTTTTCTGAACCATT[G/T]TAGAATAAGGCGCCA | 9097 |
rs554110908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:201457 | ATAGTTTGGGATAAG[A/G]TTGGCAAGGGGAAGG | 9097 |
rs554116774 | snp | G/T | 5.01433e-05 | 0.00500691 | intron-variant | USP14 | GRCh38.p7 | 18:196590 | TACAGTCGCGTGTAT[G/T]AAATATGTGACTGTT | 9097 |
rs554126514 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:160205 | GCTACTGGGGAGGCT[G/T]AGGCAGGAGAATCGC | 9097 |
rs554178174 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:189649 | CACAACGCCCAGCTA[C/G]TTTTTGTATTTTTAT | 9097 |
rs554251191 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157116 | TAAGGATCATCTGAG[C/T]TATCAGTGAATCATC | 9097 |
rs554347328 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:168976 | CAGCTACTCAGGAGG[C/T]TGAGGCAGGAGAATG | 9097 |
rs554397787 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | USP14 | GRCh38.p7 | 18:168052 | AGCAATTCTCTTGCC[-/T]TGAGCTGGGATTACA | 9097 |
rs554404425 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:181840 | CTTCTTTGTTGTTTT[G/T]CAAGAGTTAATATAC | 9097 |
rs554471848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:162311 | ACTTTTATTCCCCCC[A/G]GCAGTGTACAAGTGT | 9097 |
rs554797989 | snp | A/G | 6.60327e-05 | 0.00574561 | missense | USP14 | GRCh38.p7 | 18:211193 | CAGAAGATATCTTAC[A/G]GCTTTCTGGTGGTGG | 9097 |
rs554943291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:175492 | AAATGCCTTTTCTAT[A/G]TCATTTCTTCCTCTC | 9097 |
rs554949972 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:158875 | GCACCGTCCCCTCTC[C/T]CGGCTGGGTCGGAGC | 9097 |
rs554995102 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:205571 | TTTAGGCCAGGAGTT[A/C]GAGACTGTCCTGGGC | 9097 |
rs555035600 | in-del | -/AT | 0.0023933 | 0.0345097 | intron-variant | USP14 | GRCh38.p7 | 18:186272 | ACCAGCCTGGGCAAC[-/AT]ATAGTGAGACCCGCA | 9097 |
rs555067192 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | USP14 | GRCh38.p7 | 18:164971 | ATTTTTTTTGGGATT[C/G]AGTCTCCCTCTGTCA | 9097 |
rs555068794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:163158 | GCACCTACTGCATGC[A/G]TGCTCCTCTTGATTA | 9097 |
rs555070288 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:167167 | GGTGGGAGGCTGAGG[C/T]GGGAGGCAGAGGCAG | 9097 |
rs555107009 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:208902 | AGGCGAGTGCCACCA[C/T]GCCTGGCTAATTTTT | 9097 |
rs555174074 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | USP14 | GRCh38.p7 | 18:196159 | AACCCTGTCTCTACT[-/A]AAAAAAATGCAAAAA | 9097 |
rs555206787 | in-del | -/AAG | | | intron-variant | USP14 | GRCh38.p7 | 18:201488 | GTTGTTAAAGGGCAT[-/AAG]AAGAAGAGTGAGTGA | 9097 |
rs555345172 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:170313 | TGTCTCAAAAATAAA[C/T]AAATAAATAAATAAA | 9097 |
rs555345209 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:163634 | GGAGAAATATTGTAG[C/G]TGTTTGACAACACTA | 9097 |
rs555421881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:173554 | GTAGCTGGGATTAAA[A/G]GCATGCACCACCACA | 9097 |
rs555429489 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:180097 | ACTGTTTCTTTAGCG[C/T]GAAGGCAGAATATAA | 9097 |
rs555481673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:168375 | ACAATTTTACTTCTC[C/T]CTTTTCAATATTCGT | 9097 |
rs555486889 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:161377 | GCTGTGGAATGTTTT[C/G]CTTCTTTTCTGGGAA | 9097 |
rs555618297 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:178183 | CACCCCTATGCCCAG[C/T]TAATATTGGTATTTT | 9097 |
rs555675004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:166564 | TTTCGAACTCCTGAC[C/T]GCAGGTGATTTGCCT | 9097 |
rs555679708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:172850 | TTTTTGTGTGACTTG[C/T]TTTATTGCGATATTT | 9097 |
rs555815853 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | USP14 | GRCh38.p7 | 18:176322 | AAATGGTGGTGACTT[G/T]TTTGGTTTGTTTTAG | 9097 |
rs555843085 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:192001 | GGCCAGTTTGTTGTA[C/G]TGTTGTAAATTAAGT | 9097 |
rs555900275 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:184569 | GACTAGCCTCGGCAA[C/T]GTGGCAAAACCCCAC | 9097 |
rs555961418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:194505 | CTTTTAGTCGCATTT[A/G]GTTTCTCATTTTTCC | 9097 |
rs555975981 | in-del | -/G | | | intron-variant | USP14 | GRCh38.p7 | 18:173201 | CAAGCTCCACCTCCT[-/G]GGTTCACGCCATTCT | 9097 |
rs556075267 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:184206 | TTTTTTCTTTTTTTT[C/G]TACAGCAACCTCTGA | 9097 |
rs556124472 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:173547 | CTCCTGAGTAGCTGG[A/G]ATTAAAGGCATGCAC | 9097 |
rs556156403 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:209250 | TTTCATTATCTGTAT[A/G]AAAAAGATGTGATTA | 9097 |
rs556164630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:200671 | ATTTGGTGTGCTTTG[A/G]GGATATGTATATCTC | 9097 |
rs556246454 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:191389 | TTCTTTCATACTACT[C/T]AACATAAGCATAGAG | 9097 |
rs556281943 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | USP14 | GRCh38.p7 | 18:204919 | CTTTTTTTTTTTTTG[G/T]GACAAGGTCTTCCTT | 9097 |
rs556306387 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:195607 | GAGGGGTAAGTGGAA[A/G]GAAGGTTTTCTGAAG | 9097 |
rs556318679 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:201680 | GCAAATGAAGTCTCA[A/G]TGTTAACTGGAGAGT | 9097 |
rs556372419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:193565 | ATTATCATTCCAAAA[A/G]GCAACTTCATAACAT | 9097 |
rs556381255 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:181706 | GATGGTACGTTTGTA[A/G]TGCAAATGTTTTTTA | 9097 |
rs556391309 | snp | A/C/T | 0.00010131 | 0.00711651 | intron-variant | USP14 | GRCh38.p7 | 18:198030 | TAAAGTTGGAATTTT[A/C/T]ATTTTAATTTTTGCA | 9097 |
rs556440075 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:207040 | TGCATGTGAATATCT[C/G]GTTGTCTCAGCACCA | 9097 |
rs556532883 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP14 | GRCh38.p7 | 18:162890 | GCAACCTTCGCCTCC[C/T]GGGTTCAAGCGATTC | 9097 |
rs556547690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:192975 | AATCCTTTGCAGTTT[A/G]CAGAATGTCTTTTGT | 9097 |
rs556712501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:196298 | GAAGTGAGCGGATCA[C/T]GAGGTCAGGAGTTGG | 9097 |
rs556719514 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:165108 | TCACCACCACCATGC[G/T]TGACAAATGTTTGTA | 9097 |
rs556773759 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP14 | GRCh38.p7 | 18:188968 | ACAGGCGTGAGCCAC[C/T]GTGCTTGGCCTTTGG | 9097 |
rs556843130 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157515 | CTTATCCATAAGAAG[C/T]GACTCCTTGCCCATT | 9097 |
rs556857767 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:211001 | GTGTGGTCACTGGGT[C/G/T]GCACTTGGAGGACTG | 9097 |
rs557012364 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:196538 | CAAAAAAAAAAAAAA[A/T]TAAGTAAGTTTTTGT | 9097 |
rs557200258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:164175 | GGATGTATTAAAAGT[A/G]TTAGTTTTATTTTGT | 9097 |
rs557255230 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:161627 | AATGCTTTGTACCGG[G/T]CTTGTCATTAAATGA | 9097 |
rs557272402 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:162175 | GCTCCCACTTTTTCG[C/G]CTGTTGTGAATAATG | 9097 |
rs557315735 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:168679 | ACCTCAAGTGATCTG[C/T]CTGCCTTGATCTCCC | 9097 |
rs557325085 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:169852 | TTTGATGTTACTTTT[G/T]TAATTGTTTTGGGGT | 9097 |
rs557364249 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212668 | GTGATTTTAAAGTGA[C/T]AGTAGAAAATACCAA | 9097 |
rs557457456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:160258 | GTAGTGAGCCAAGAT[C/T]GCGCCATTGCACTTC | 9097 |
rs557483835 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:192167 | TGATTTTTGATTGAA[A/T]GTTTTTGATCTAATG | 9097 |
rs557492909 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:172785 | ACATAATGCTGTTGC[A/G]TACTTCACAGACTGA | 9097 |
rs557493572 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | USP14 | GRCh38.p7 | 18:204996 | CCTCCCACCTCACCC[G/T]CCCAAGTAGCTGGGA | 9097 |
rs557518464 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:190080 | TAATGGGTCTGGCTC[A/T]TGATGTTTAGTGTAT | 9097 |
rs557553731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:166471 | CCGAGTAGCTGGAAT[C/T]ACAGGTGTGCACCAC | 9097 |
rs557682060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:187355 | GGTGTGTAGTAATGC[A/G]TACTTCTTACTTTCA | 9097 |
rs557697291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:171944 | TGTAAATAGGAAGAA[A/G]CTAGAATTAGAAGTG | 9097 |
rs557745338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:179369 | TAGTACTATATAAGT[A/G]TTTACTATTACTATT | 9097 |
rs557772254 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | USP14 | GRCh38.p7 | 18:203373 | CTATTGTCTTTTTTA[-/T]TTTTTAACTGTACAC | 9097 |
rs557808397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:179990 | AAAGGCAAGACTAGT[A/G]TGATTATTCTCTTAT | 9097 |
rs557869888 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:173346 | TCTATCTCCTGACCT[A/C]GTGATCAGCCCGCCT | 9097 |
rs557882604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:166952 | AAATACTTACCTTTT[C/T]CCATTGACTTGTGTT | 9097 |
rs557882658 | in-del | -/AATC | | | intron-variant | USP14 | GRCh38.p7 | 18:193072 | ATCGTCCAGATTATA[-/AATC]AATGATGTCTGTCGT | 9097 |
rs557986233 | in-del | -/AGTT | 0.00874735 | 0.0655527 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213426 | TCAAGTAGAAATGGG[-/AGTT]AGTTAGTTATACCAG | 9097 |
rs558058697 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:197720 | AATATATTTGTGATT[A/G]TAGACTTTCGTTATA | 9097 |
rs558060286 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:168206 | GCTAGGATTACAGGC[A/G]TGAGCCACCGCACCC | 9097 |
rs558086272 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:195440 | TCACATCTTGGGTAT[C/T]AATAAAACATACAAG | 9097 |
rs558101221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:190779 | GAAAGATTCTCAGTA[C/T]TTTTGACTGTAAAAC | 9097 |
rs558159224 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:194468 | ATTTACAGAAAAGTT[C/G]TAAGAATTCACCAGT | 9097 |
rs558162609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:191515 | GTAATCCATTTGCCT[A/G]TCAAAGTATAGAACA | 9097 |
rs558230039 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:184151 | TAAAAAAATAAAAGT[C/G]AAAGTTACTTTTTTC | 9097 |
rs558236755 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:198012 | TCTACATTAATATTT[A/G/T]TATAAAGTTGGAATT | 9097 |
rs558300470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:200895 | CAACCTCTGACTCCC[A/G]GGTTCAAGAGATTCT | 9097 |
rs558338671 | snp | G/T | 0.000165728 | 0.00910144 | intron-variant | USP14 | GRCh38.p7 | 18:163464 | TAAAGGTAAAATGTA[G/T]TCCAAATTTTCATCA | 9097 |
rs558420658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:201510 | AGAGTGAGTGAGTCA[C/T]GCTCTGTCTTATGAT | 9097 |
rs558455318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:204461 | CACAGATTTTATTTT[C/T]AACTGTATCTGAATT | 9097 |
rs558548415 | in-del | -/C | | | intron-variant | USP14 | GRCh38.p7 | 18:183228 | TTGGTAGTTATTTGT[-/C]CACTATTTTTGTGTG | 9097 |
rs558719961 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:173861 | TGCCTTTGTTGAAAA[C/T]CAGTTGACCATAAAC | 9097 |
rs558767419 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212403 | CTGGAGGTTGAGTTC[A/G]AGACCAGCCTGGCCA | 9097 |
rs558768838 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213704 | GATTAAAAACGATGA[G/T]GACCTCATCTTAGAG | 9097 |
rs558790857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:199717 | CGTTGCACTGTTGGC[C/T]CTGAGTTCAATGTTA | 9097 |
rs558822142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:197453 | TTGAATGAATAAGCT[A/G]TTCTAGAATGCTTTA | 9097 |
rs558832753 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:196380 | ATACAAAAAATTAGC[C/T]GGGAATGGTGGCGTG | 9097 |
rs558845730 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:177455 | AAAAATTCTGTAGTG[A/G]TGGCTTAGTACTGCT | 9097 |
rs558909259 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:176253 | TAAATTTTTTAAAAT[A/T]TTGAAAATTTTTATA | 9097 |
rs558939531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:198795 | AAAAGAATTTTTTAA[C/T]TTTATAAAAGGGTGT | 9097 |
rs559001070 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:192103 | TGACCTACAACCTTA[A/C]GTGACCTATTTAATG | 9097 |
rs559069809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:175704 | TTTTGCTATCAGTGT[A/G]ATGTTAGTCTTATAC | 9097 |
rs559278512 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:160933 | ATTTTATTTTATTTT[A/T]TTTTATTTTTTGAGA | 9097 |
rs559282761 | snp | A/G | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:201800 | GGTCTAGATGATAGT[A/G]GATTGGTGGTAATAA | 9097 |
rs559343169 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:208542 | TTCCCTTTCAGCAGT[C/G]ATTTCACTATATCCT | 9097 |
rs559344199 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:168547 | TCATGTGATTCTCCT[G/T]CCTCAACCTCCTGAG | 9097 |
rs559349196 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:164493 | GAGTCTTGCCCTGTT[G/T]CCCATGCTGGAGTGC | 9097 |
rs559374588 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:194074 | GGGTTCTGATTTCTC[G/T]GTCTCCTTACCAGTA | 9097 |
rs559406278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:162418 | TGAAGTGGGATTTCT[A/G]TATATTTTTAAATGA | 9097 |
rs559409061 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:201053 | TGATCCGCCCACCTC[A/G]GCCTCCCAAAGTGCT | 9097 |
rs559457165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:172981 | AAGTCAGTTGATCAC[A/G]TTTTTTAGTGATTTG | 9097 |
rs559493888 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:208050 | TGGTGGAACAGTCTG[A/C]TTAGAGATTTTACTT | 9097 |
rs559499269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:187601 | TATTTGACTTTCAGT[A/G]AGATGGATTTTTTTC | 9097 |
rs559548069 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:165982 | GTTAGTAAAAATATT[A/T]CTCTGGACTAATCAT | 9097 |
rs559618703 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:208937 | TTTTATTAGACACAG[G/T]GTTTCATCATGTTGG | 9097 |
rs559666833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:179574 | CATTCATTTTCATGG[C/T]TTTTTTTTTTGCTTT | 9097 |
rs559678791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:170801 | TTGTAAGTGGGAGCC[A/G]AGCAATGAGAATACA | 9097 |
rs559713211 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:161022 | GACCTCCACCTCCTG[A/G]TTTCAAGCGATTCTC | 9097 |
rs559735684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:171371 | TTTAAGTTGAAACCA[A/G]TGCTCGTTTACCATT | 9097 |
rs559737534 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:164676 | CCAGTTTGGTCTTGA[A/T]CTCCTGACCTCAAGT | 9097 |
rs559802801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:203765 | CAGGCGCCCGCCACC[A/G]TGCCCGGCTAATTTT | 9097 |
rs559863952 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:166034 | GATTTTTATTCAACA[C/T]ATTGAAAGGAAAGTA | 9097 |
rs559947069 | snp | A/G | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213719 | TGACCTCATCTTAGA[A/G]CCCTAAAGGGAAATG | 9097 |
rs559956738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:188418 | CTTTCAATATATAGC[A/G]CTGAATTTAATTTGC | 9097 |
rs559994985 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | USP14 | GRCh38.p7 | 18:173383 | CCCAAAGTGCTGGGA[C/T]TACAGGCTTGAGCCA | 9097 |
rs560012300 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:169985 | ATTCCCTGAGACAAG[A/T]CAGTATTGAAATTAG | 9097 |
rs560012926 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:206352 | CTATCTGTATATCCT[C/G]TTTTGTAAAATGCTT | 9097 |
rs560020602 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:159036 | GGTGTGTCCTGGGGC[G/T]CTGGGCCAGGCTGGA | 9097 |
rs560075320 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:193982 | GGTCATATGATTACT[A/G]TATTTAACCTTTTGA | 9097 |
rs560122652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:184267 | TAAATTTTCTCAAGA[A/G]AGTGCACTTACTAAC | 9097 |
rs560181783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:176082 | TCGTTTTCCTCTCTA[A/G]TATTGGCAAATTATG | 9097 |
rs560184392 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, downstream-variant-500B | USP14, LOC105371951 | GRCh38.p7 | 18:158534 | GTTTTGCGTGTTGCT[A/G]CGTCATCGCCAGTGG | 9097 |
rs560185316 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:213920 | TGAGGTTTTAGACTT[A/C]ATTTCTTTTAAAGTT | 9097 |
rs560189274 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | USP14 | GRCh38.p7 | 18:186752 | GGGAGACTGTGTCTC[-/A]AAAAAAAAAGAGAAA | 9097 |
rs560212275 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:198374 | CAAGTAGCTGGGATT[A/G]CAGGTGCATGCCACC | 9097 |
rs560224883 | in-del | -/TTG | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:197178 | GCAGGGCCTTTGCTC[-/TTG]TTCTTTGGCTGTCAG | 9097 |
rs560263424 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:183670 | CTTCTGTTCTTTTTT[A/T]TAACTCCTTATTCTT | 9097 |
rs560328639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:175143 | TAATTTTTATAATTG[A/G]CTTTGTATCCTGTGA | 9097 |
rs560425100 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:185061 | CAGTATCACATGGCC[C/G]TATCTGTTGTATTGG | 9097 |
rs560783506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:200004 | TAGACAAAAGCATTA[C/T]TGACATGGTTGCATA | 9097 |
rs560859557 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:196312 | ATGAGGTCAGGAGTT[C/G]GAGACCAGAGCCTGG | 9097 |
rs560961063 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:173662 | TCCTGACCTCAGGTG[A/T]TCCGCCCACCTCGGC | 9097 |
rs561036754 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:188668 | ACTCAGCTTTTTTGG[G/T]GTATTTTATTTTATT | 9097 |
rs561165341 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:188868 | ATTTTTAGTAGAGAC[A/G]TGGTTTCACCATGTT | 9097 |
rs561181297 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:196291 | ACAGGCTGAAGTGAG[C/T]GGATCATGAGGTCAG | 9097 |
rs561283668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:174272 | CGTTTTTCTTTCTTT[C/T]TTTTTTTTTTTTTGA | 9097 |
rs561309602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:190296 | TTTCTGTTGGGTATA[C/T]ATGAGTATGTATGCA | 9097 |
rs561314335 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:197829 | TACTTTAGATGCTCA[A/G]TCTGTAGTCAGAATT | 9097 |
rs561315326 | snp | C/T | 0.000265587 | 0.0115205 | intron-variant | USP14 | GRCh38.p7 | 18:197608 | CTTTGTCTTTTTTTA[C/T]ATTACAGGATGCTAA | 9097 |
rs561343477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:162500 | TGACACTTTTCAATT[C/T]TCCCAGATTTCTTAT | 9097 |
rs561379154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:190982 | ACAAAAAAAAGGTTG[A/G]TAATTCATTAGTATA | 9097 |
rs561423535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:168714 | TGCTGGAATTACAGG[C/T]GTGAGCCACTGTGCC | 9097 |
rs561485880 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP14 | GRCh38.p7 | 18:169349 | CTGGGCAACAGAGCA[A/G]GACTCTACCTCAAAA | 9097 |
rs561517689 | in-del | -/TG | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:209854 | ATTTGGAAGGTAGAC[-/TG]TATTTTGTCTCTGTG | 9097 |
rs561587226 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:211836 | TGTCCAGCCTATTGC[A/T]GGCTTTTCCTGACTT | 9097 |
rs561608694 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP14 | GRCh38.p7 | 18:163101 | TCAGTTTCTTTAACT[A/G]TGAAATGAGAAGTTA | 9097 |
rs561702397 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:173274 | CACCACACCCGGCTA[C/T]TTTTTTTGTATTTTT | 9097 |
rs561715027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:193304 | CTTAAAGGATAGAAA[C/T]AACTGGTTTCTTCAT | 9097 |
rs561744974 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:160335 | GAAAATTACATATCT[A/G]GATTATTAAATGGTT | 9097 |
rs561820979 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | USP14 | GRCh38.p7 | 18:177100 | TTTAGGTGCTTTTTT[A/T]AAAAATATCCTTAAG | 9097 |
rs561821160 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:171537 | CTTCCTGCTCAGAAA[G/T]ATTCCTTTCAAAATA | 9097 |
rs561858432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:207837 | TTTATTCTTTTTGAT[A/G]CTTTTGTAAATGGCA | 9097 |
rs561869157 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:201969 | GCTGAATAAACTTGG[G/T]TAAATGTTAAAAAGC | 9097 |
rs561879877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:172047 | GGAGTTTGAGACCAG[C/T]CTGGGCAACACAGTG | 9097 |
rs561937476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:165362 | GGCTACCCCCACTGG[A/G]CAGTAAAACACACGT | 9097 |
rs562000000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:209099 | CATGTTAGGGTTTAA[C/T]TCTGCTTTTTTGATG | 9097 |
rs562036588 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:161127 | GAAACGAGGTTTCAC[A/C]GTATTGGCCAGGCTG | 9097 |
rs562100301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:175060 | TTACAAGCGTGAGCC[A/G]CTGCACCCAGCTGTG | 9097 |
rs562114104 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:186536 | GGCGGGCAGATCACC[A/G]AAGGTCAGGAGTTCA | 9097 |
rs562162148 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:169959 | CCTCCTCCCTCTTCT[C/G]GAGCCTCCCTATTCC | 9097 |
rs562177673 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:178579 | TAGAAGTTTCATCAC[A/G]AAAAAGTTTCTTTGT | 9097 |
rs562252626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:161671 | TAATTGAACTGATGA[C/T]AGAGTTGGGATTTGG | 9097 |
rs562267503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:205343 | ACCTAGTGTTGACCT[C/T]GATGCAGTCAAAATA | 9097 |
rs562272183 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:162678 | ATGGGGGCTGCGAAA[C/T]TTATCATTTTGGGAA | 9097 |
rs562372439 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:182826 | AACAGTCTGGAGGCA[G/T]GAGACTGCAACATAC | 9097 |
rs562375983 | in-del | -/CAAGCAGT | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:210916 | TGTGGGTGGAAAAGG[-/CAAGCAGT]GCTCTAGTGGTGTCA | 9097 |
rs562397123 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:165355 | AAAGACAGGCTACCC[C/G/T]CACTGGGCAGTAAAA | 9097 |
rs562397473 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | USP14 | GRCh38.p7 | 18:179471 | AAATACATACATTTT[A/T]TCCTGAATTTAAATG | 9097 |
rs562455350 | snp | A/T | 0 | 0 | downstream-variant-500B | USP14 | GRCh38.p7 | 18:213783 | TCTTCTGCTACTACT[A/T]CTTAGTGCTTTGCTG | 9097 |
rs562526832 | in-del | -/TGT | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214076 | GCTCCTTAGCTTTGC[-/TGT]TGTTGTTATAGTGTA | 9097 |
rs562582258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:163775 | AGGGTTTCAATGTAC[A/G]GATTTCATCACCCAG | 9097 |
rs562634016 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:183553 | TCCGTGTTTTAAATT[G/T]TTATAATTTTTATGT | 9097 |
rs562667523 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:190060 | TTGTCTGGCTGATGA[C/G]TGGGTAATGGGTCTG | 9097 |
rs562703635 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:192272 | AATACTTTCAGAAAA[C/T]GTTTGTTTTAGCTGG | 9097 |
rs562722246 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:171533 | GAGACTTCCTGCTCA[A/G]AAAGATTCCTTTCAA | 9097 |
rs562726617 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP14 | GRCh38.p7 | 18:196333 | CAGAGCCTGGCCAGC[A/G]TGGTGAAACCCCATC | 9097 |
rs562771924 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP14 | GRCh38.p7 | 18:184954 | GAATCCCATCATACT[C/T]CTGGAGTTAGATTCT | 9097 |
rs562781673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:198268 | TTGAGACGGAGTTTC[A/G]CTCTTGTCGCCCAGG | 9097 |
rs562867174 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:184438 | ACTTAGCAGAACTTG[G/T]CTTTGGCAGGTTCTA | 9097 |
rs562919966 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:174853 | TGATCATGGCTCACT[C/G]TAGTTTCTGCCTCCC | 9097 |
rs562962642 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, downstream-variant-500B | USP14, LOC105371951 | GRCh38.p7 | 18:158381 | TGGGGCCCCGCGCCC[A/G]TCCCTCACTTGCTCC | 9097 |
rs562971458 | in-del | -/T | 0.271432 | 0.24908 | intron-variant | USP14 | GRCh38.p7 | 18:162802 | TGAAGTCTCAGTTTC[-/T]TTTTTTTTTTTTTGA | 9097 |
rs563100579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:187666 | ATTTTGTAATGTTAG[A/G]TGAATTTTCCCTTGA | 9097 |
rs563182777 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:201955 | TCCACTGCTTTGCTG[C/G]TGAATAAACTTGGTT | 9097 |
rs563200040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:191839 | GGGTGTGTAGTATGT[A/G]CACATAGTTTAATCA | 9097 |
rs563244626 | in-del | -/A | 0.00755907 | 0.0610114 | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:213989 | ATTAGATAGATAGAT[-/A]GATAGATAGATGATG | 9097 |
rs563247425 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:202669 | AATCCACAACAACGT[A/T]AATTATTTGATGCCT | 9097 |
rs563257049 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:210101 | AAATTTACATCTTAC[C/T]CCATATTTACTTATT | 9097 |
rs563263340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:195904 | AAGAAAGAGAGAGGG[A/G]GGGCTCAGAAGTTGT | 9097 |
rs563360215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:180395 | TGGATGAGTAGTATT[A/G]TTTTGTTTTGCTTTC | 9097 |
rs563452930 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:199838 | TGATCAAAGGCTGGC[A/G]GGAATCTAATCCTGT | 9097 |
rs563498033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:161072 | AGCTGGAATTACAGG[C/T]GCCTGCCACCATGCC | 9097 |
rs563511282 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:211649 | GTTTACTGCACACCT[A/G]TTACCTATTATTTGC | 9097 |
rs563535149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:163055 | TACTGGGATTACAGG[C/T]GTGAGCCACCACGCC | 9097 |
rs563572283 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:196410 | GTGCCTGTAATCCCA[A/G]CTACTCTGGAGGCTG | 9097 |
rs563581220 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:160155 | TAAAAATACAAAAAA[C/T]CAGTCGAGAGTGGTG | 9097 |
rs563649645 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:203811 | GAGATGGGGTTTCAC[C/T]GTGGTCTCAATCTCC | 9097 |
rs563726838 | snp | A/G | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213441 | GAGTTAGTTATACCA[A/G]TGTTGTTTTTAACTA | 9097 |
rs563745226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:168079 | TACAGGCGCCCACCA[C/T]CACGCCCAGCTAACT | 9097 |
rs563758737 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:165610 | GTATGTTATCCATAT[C/G]TTATATATGAGGAAA | 9097 |
rs563796935 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:193517 | TTTATCCACAGAGTT[A/G]TGCAAATATTACTAA | 9097 |
rs563824445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:181187 | CCTTTTTGGCTGTTA[C/T]GAGTAATGCTGCAGT | 9097 |
rs563827517 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:159721 | AATGGCTCTTGAAAT[A/G]TTCTAATACTTAAAC | 9097 |
rs563885050 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:191202 | AAATGTAATGATTTT[C/T]AGGTTTTTAAAAATG | 9097 |
rs563886245 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:173624 | TCAGACTGGTCTCCA[G/T]GTTGGTCAGGCTGGT | 9097 |
rs563927083 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:183929 | GCTTTCTGGCTAGCA[A/C]CCTTGGGAGTGGCTG | 9097 |
rs564070177 | in-del | -/A | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:156924 | CTTTACAAAACATAC[-/A]AAAAAAAATTAGCCG | 9097 |
rs564092295 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP14 | GRCh38.p7 | 18:178461 | TCCTTAAGCTTTATT[C/G]AGGTACAATTTATAT | 9097 |
rs564134155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:165827 | CCTTTAGGAAGTTAC[C/T]GTTCCATTTTAAAGC | 9097 |
rs564150675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:199446 | GCATTTTGAGTTGCC[C/T]GATACACACAGTCCC | 9097 |
rs564227099 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:184803 | AAGAGAGTGGGATGT[A/T]TAATGATGGAGGGTA | 9097 |
rs564256234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:208685 | TCCTGTTATGTTTCT[A/G]TTGATTCTAGTTTGA | 9097 |
rs564302114 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:176151 | CAGTTTCATTGATTG[C/T]GTCCCCCCAAAAAAA | 9097 |
rs564308936 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:176432 | ACCTTGGACTACAGG[G/T]GTGTGCCACCACACA | 9097 |
rs564400806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:166682 | AAAATCTGCATATAG[A/G]ATAAATTTTATTCTG | 9097 |
rs564427612 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:177581 | ACTAATTTCCTAATT[G/T]TAATCATCATCTGGA | 9097 |
rs564511558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:182558 | TATCAGTGAACAAGA[C/T]ACAGTATCTGTCTTC | 9097 |
rs564533726 | in-del | -/TTC | 0.00914312 | 0.0669923 | intron-variant | USP14 | GRCh38.p7 | 18:209198 | TGTTTTTAAATGTGT[-/TTC]TTTGTATAGTTTTTT | 9097 |
rs564655854 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:211918 | TGTCTCTCTCTGATG[C/T]ACTGTGGATTGTACA | 9097 |
rs564733099 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:193773 | TATCAGTACTTCATT[C/G]TTTTTTATTGCTAAA | 9097 |
rs564784407 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:189232 | CATTCAATTTTTTGA[G/T]TTGTCTGATTCATCC | 9097 |
rs564826262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:174987 | TGCCATGTTGGCCAG[A/G]CTGTTCTCGAACTGG | 9097 |
rs564845637 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:181610 | TCTTTTCTTCTATAC[A/T]ATAAGCTGTCATTTT | 9097 |
rs564929558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:174390 | CCTTCCTCAGCCTCC[C/T]GAGTAACTGGGATTA | 9097 |
rs565074850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:196343 | CCAGCATGGTGAAAC[C/T]CCATCTCTACTAAAA | 9097 |
rs565085358 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:175276 | TTCTCTTTTTTTCTT[C/T]ATTGCAATGCTTAAG | 9097 |
rs565100538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:198217 | CTGATTGATTGGTGG[C/T]GGGTAGAAGAAAAAT | 9097 |
rs565136641 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:171360 | TAGCTAATGACTTTA[A/C]GTTGAAACCAATGCT | 9097 |
rs565185436 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:184166 | GAAAGTTACTTTTTT[C/T]GCTTTTTGGTTTTTA | 9097 |
rs565243612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:205656 | TGTGGTGGCATACAC[C/T]GGTAGTTCTAGCTAC | 9097 |
rs565248472 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:173333 | AGCCAGGATGGTCTC[A/G/T]ATCTCCTGACCTCGT | 9097 |
rs565369129 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:184293 | CTAACGTAATTGATA[C/G]AAGATGTCATGGATG | 9097 |
rs565464164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:206734 | GTGAAACCCTGTCTC[C/T]ACTAAAAATACAAAA | 9097 |
rs565587614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:178071 | GTCGCGCAGGCTGGA[A/G]TGCAAGTGGTGTGAT | 9097 |
rs565604068 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB, downstream-variant-500B | USP14, LOC105371951 | GRCh38.p7 | 18:158322 | TGGCCAGTGCGCGCA[A/G]GGCGATGGGCGGCAG | 9097 |
rs565664978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:185858 | ACCACTATGCCCAGC[C/T]GATTTTTTTTTTTTT | 9097 |
rs565716739 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:199597 | CTGTTTAAGATGACC[A/C]CCCAAGCACAGGGCT | 9097 |
rs565776297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:178831 | TTTTTTTGGCAAATA[A/G]AATTATGTTATATGT | 9097 |
rs565791349 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:176250 | TTTTAAATTTTTTAA[A/C]ATTTTGAAAATTTTT | 9097 |
rs565922949 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:192707 | AGACCAGAAGAGAAG[A/T]AAAGGAAAGGTGGGA | 9097 |
rs565924266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:200450 | GTCGTTCTGCCATTG[C/T]ACTGTCTTGCAGTTG | 9097 |
rs565969239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:166884 | ATACCAAAATACATT[C/T]CAGATGACTTTTTTT | 9097 |
rs566031004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:167508 | ACATAGAGGTTTTGC[A/G]TGAGTGGTTTTTTTT | 9097 |
rs566037228 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:192211 | AGTTATTTCAGAGAT[G/T]GTGTTATTTTATTTT | 9097 |
rs566090256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:163952 | AGAGAACATGCAGTT[C/T]GCTTTTCTGTTCCTG | 9097 |
rs566107096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:195302 | TTTCAGCCTTCCCTC[C/T]AAAAATATTTTTTAA | 9097 |
rs566126625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:197440 | CAGCAGATGTCTGTT[A/G]AATGAATAAGCTATT | 9097 |
rs566184565 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:202091 | AGTAGGTTATTTTAA[A/T]TCTAATTTCTTTTTT | 9097 |
rs566189827 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:197938 | TTGAAGGATTTTACT[G/T]TAAGGGACTACATTT | 9097 |
rs566237716 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:173160 | GTTGCCCAGGCTGGA[C/G]TGCAGTGGCACGATC | 9097 |
rs566262829 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:201463 | TGGGATAAGGTTGGC[A/C]AGGGGAAGGGTTGTT | 9097 |
rs566331845 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:208811 | AGTGCATAGGTACGA[C/T]CCCGGCTCAGTGCAA | 9097 |
rs566339497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:205417 | GGGCCACTTTTCTTC[C/T]GCCCTACCCCTTCCT | 9097 |
rs566428868 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157117 | AAGGATCATCTGAGC[C/T]ATCAGTGAATCATCA | 9097 |
rs566740936 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:167935 | TTGATTTTTCTCTCT[-/T]TTTTTTTTTTTTTTT | 9097 |
rs566844486 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:171194 | TAGCTAAGATTGTTG[A/C]TGAAGGTAGCTACAC | 9097 |
rs566870518 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:206815 | CTGAGGCAGGAGAAT[C/T]GCTTGAACTGGGGAG | 9097 |
rs566908249 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:169220 | ACATGGTGAAACCCC[A/G]TCTCTATTAAAAATA | 9097 |
rs566912771 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | USP14 | GRCh38.p7 | 18:206095 | AATGCAGTTGTTAGA[C/T]TGCATGGTAGTTGCA | 9097 |
rs566934934 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:158854 | GGCGGCGCGGAGATG[A/C]CCCAGGCACCGTCCC | 9097 |
rs567040008 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:184118 | ACCAAAAGAAGTATT[G/T]TTTGTTTTTCCTTTT | 9097 |
rs567100655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:175569 | TATATTCTTGGGATA[A/G]ACCCCACTTGGACAT | 9097 |
rs567187173 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP14 | GRCh38.p7 | 18:194521 | GTTTCTCATTTTTCC[A/G]TTATGCATGTAATTT | 9097 |
rs567217016 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:205318 | CTCAAAGTACTTCAC[A/G]TAAAACCTTACCTAG | 9097 |
rs567229330 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:204248 | TCCATTATTTTCACA[A/G]CAGCTTGTCCAATAT | 9097 |
rs567229726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:161424 | TAGTCTCTGACTAAC[A/G]CCTAATCTTTTCTTG | 9097 |
rs567295323 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:185036 | ATTCTATAAATTACT[C/T]CTCAAAAGACAGTAT | 9097 |
rs567302248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:173420 | CCGGCCTATATTGTC[C/T]GTTTTTTTGAGACGG | 9097 |
rs567304252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:167579 | GGCATGGTCATGGCT[C/T]GCTGCAGCTTTAAAC | 9097 |
rs567329784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:187017 | TTGGCAGTTGTTATC[C/T]CAAAAGGTAGAAAAA | 9097 |
rs567389111 | snp | C/T | 1.68394e-05 | 0.00290162 | intron-variant | USP14 | GRCh38.p7 | 18:210054 | ACATTCTCATTTTAA[C/T]TGAGTTATTGTATGT | 9097 |
rs567646044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:189576 | CAGCCTCCGCCTCCT[A/G]GGTTCAAGTGATTCT | 9097 |
rs567660848 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:182896 | TGATAGATGGGAGAT[A/T]AGCAGGGGCCAGCCA | 9097 |
rs567702457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:181845 | TTGTTGTTTTTCAAG[A/G]GTTAATATACTTTTA | 9097 |
rs567722581 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157603 | TCTAGTTCTCTTGCT[A/G]TTGCCACCACACCTG | 9097 |
rs567750309 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP14 | GRCh38.p7 | 18:173488 | GTGATCTCAGCTCAC[C/T]GCAACCTCCGTCTCC | 9097 |
rs567760330 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:173920 | CTTCCATTGATTTTT[A/G]TATGTACCTTTGTAC | 9097 |
rs567805698 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:162044 | TCATATAACCAGAAT[C/G]ATCCATGTTGCAGCA | 9097 |
rs567822425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:203841 | CTGACCTCTTGATCC[A/G]CCCGCTTTGGCCTCC | 9097 |
rs567844628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:203522 | TAGTGCCCTAGACCA[C/T]GTCCTCAGCTTCAGG | 9097 |
rs567906541 | snp | C/T | 1.64836e-05 | 0.0028708 | synonymous-codon | USP14 | GRCh38.p7 | 18:163408 | TGCGTTGACTGGAGT[C/T]CAGCCTGCCAGACAG | 9097 |
rs567949229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:192687 | TCCATATTTCTGGTC[A/G]TGCAAGACCAGAAGA | 9097 |
rs567977635 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:173284 | GCTATTTTTTTTGTA[-/T]TTTTTTTTAGTAGAG | 9097 |
rs567979616 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:188848 | ATGCCCAGCTAATTT[C/T]TTGTATTTTTAGTAG | 9097 |
rs567980790 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:211633 | GATTCAGCAGTCAGA[C/T]GTTTACTGCACACCT | 9097 |
rs567987343 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:173498 | CTCACCGCAACCTCC[A/G]TCTCCCAGGTTCAAG | 9097 |
rs568010449 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:185164 | TTTTTCTTATTTTTT[A/T]TTTATTTATTTTCGA | 9097 |
rs568071265 | snp | A/G | 3.30077e-05 | 0.00406236 | synonymous-codon | USP14 | GRCh38.p7 | 18:166801 | GGATGATGATTGGGG[A/G]AACATCAAAATAAAA | 9097 |
rs568118126 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:164956 | TCTATTATTATTATT[A/T]TTTTTTTTGGGATTG | 9097 |
rs568157132 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:185692 | TTAAAATTTAAAAAA[A/T]TTTTAAATTATTTTT | 9097 |
rs568176810 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:201400 | GTGGGACATGGATTA[A/T]GTTGATAAACAAGAT | 9097 |
rs568282798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:171725 | GTTTCCCTATAAAGT[C/T]ATTTCTCCATGAATC | 9097 |
rs568323125 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:198614 | GATAATGGGATTATT[C/G]ATTATGTTTTGATTA | 9097 |
rs568332036 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:160131 | AACATGTTGAAACCC[C/T]GTCTCTACTAAAAAT | 9097 |
rs568339241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:159349 | ATGAATACACATATC[C/T]CCGGGGTGTCATTTC | 9097 |
rs568388848 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:199534 | TTTAGCAGGAATGTT[A/T]GAACTGTTGTTTTAA | 9097 |
rs568447805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:160732 | GTTTTGGTTTAATCC[C/T]GTAGCATCTTTAGCT | 9097 |
rs568614257 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:167214 | TTGAACCTGGGAGGC[A/G]GAGATTGCAGTGAGC | 9097 |
rs568634428 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:197281 | CTGATGACCTTATTG[C/G]AACAGCACACTTCCC | 9097 |
rs568654781 | in-del | -/TTA | 0.0023933 | 0.0345097 | intron-variant | USP14 | GRCh38.p7 | 18:190173 | TCCTGTACTACCAAG[-/TTA]TTATCCATTCTTCTG | 9097 |
rs568739510 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:173734 | GGTCTATTATCTGTT[C/T]TGAGTAAATTCTTGT | 9097 |
rs568789587 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:162837 | GAGTCTCGCACTGTC[A/G]CCCAGGCTGGAGTGC | 9097 |
rs568856222 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:178001 | ACAGAAATAATTTTA[C/T]TAGTGTTTGTTTGTT | 9097 |
rs568969250 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157106 | TAAAAAATGCTAAGG[A/C]TCATCTGAGCTATCA | 9097 |
rs569088063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:200283 | AAAATGAGAGTAACT[A/G]TAGGGTTGTTTGTGG | 9097 |
rs569125904 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:168933 | TACAAAACAATTAGC[C/T]GTGCATGGTGGCAGG | 9097 |
rs569179733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:197104 | ACTACCACTCTGTCC[C/T]TTGCTTGCCTCTCTC | 9097 |
rs569216837 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:194283 | TAGTGAGAAAGTGTG[A/G]TCATTTATATCTACT | 9097 |
rs569303143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:176196 | TTCATTTATTACTTC[A/G]TTTATTTTTTCTCTT | 9097 |
rs569304840 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:170233 | TGCTTGAGCCTGGGA[A/G]ATGGAGGTTGCAGTG | 9097 |
rs569328841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:164258 | GTTGGAAAATTTTAT[C/T]TCAGTTTAAAAATGT | 9097 |
rs569366852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:171083 | GCAGAAGTTGGTTCA[C/T]GAGGTTTAAAGAAAG | 9097 |
rs569375810 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:172518 | GATAAAATGCTATTA[A/C]ACAGCACCGCAAGCT | 9097 |
rs569397467 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:191228 | AAATGAACACACATA[A/G]TTCAGGCATTATTGT | 9097 |
rs569418524 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:190551 | GTACTTTATTTCACT[A/G]TGGGTAAGGATTGTG | 9097 |
rs569638708 | snp | C/T | 4.74327e-05 | 0.00486971 | intron-variant | USP14 | GRCh38.p7 | 18:178896 | AAACATTACCAACTT[C/T]TAAGGATTTTCATGA | 9097 |
rs569642145 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:166963 | TTTTCCCATTGACTT[G/T]TGTTGGGCTCTTTCT | 9097 |
rs569652219 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:176107 | ATTATGATTTGTCTG[C/T]TTCCTCTATCATCAA | 9097 |
rs569699174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:179632 | TTGCTCTGTCACCCC[A/G]GCTGGAGTGCAGTGG | 9097 |
rs569702412 | in-del | -/AAT | 0.00119737 | 0.0244387 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212913 | ATGATAACTATTAAA[-/AAT]AATAGAAAATAACAG | 9097 |
rs569763732 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213590 | GAGGCCATCATCTCA[A/G]CATTAGAGTTGTGCT | 9097 |
rs569776165 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:204971 | TCTCAACCTCCCAGG[C/T]GCAAATGATCCTCCC | 9097 |
rs569818186 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:180715 | CTTCTTTCATTTGGC[A/G]TGTTCCCATGGTTCA | 9097 |
rs569887447 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:191091 | TATATAGCTAATTAC[A/G]TACCCAAGTGATGTT | 9097 |
rs569938223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:186926 | ACATCTTGATGCATA[A/G]GATTCTTTGGATCAA | 9097 |
rs569949171 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:176248 | GGTTTTAAATTTTTT[A/T]AAATTTTGAAAATTT | 9097 |
rs570009302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:196119 | CAAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 9097 |
rs570041526 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:199925 | GTAGAACATAATTAC[C/T]GTGACTAACAAAATC | 9097 |
rs570055248 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:161560 | ACATAGTTAATTACT[C/T]TAGCCTCCTCCCACC | 9097 |
rs570185181 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:167545 | CAGGGTCTCACTCTC[A/T]CGTATGCCGGAGCAC | 9097 |
rs570218711 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:184547 | TCACTTGAGCTTAGG[A/T]ATTTGAGACTAGCCT | 9097 |
rs570230640 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:161927 | ATACAGTTCTATAGC[A/T]TTAAATATATTCACA | 9097 |
rs570294783 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:188869 | TTTTTAGTAGAGACG[G/T]GGTTTCACCATGTTG | 9097 |
rs570382454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:185401 | CACAAGTCATCTGCC[C/T]GCCTCAGCCTCCCAA | 9097 |
rs570387952 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:164828 | TTTTGTTTAAAAAGA[A/G]AAGAAACCTAATTTT | 9097 |
rs570390949 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:191964 | CTATGGTTTGAATAG[G/T]CATTTGAAAAGGAAT | 9097 |
rs570449776 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, downstream-variant-500B | USP14, LOC105371951 | GRCh38.p7 | 18:158593 | AGCCGCCGCCACCAC[C/T]GCGCCTCCGCCTCGG | 9097 |
rs570470371 | in-del | -/T | 0.315704 | 0.241212 | intron-variant | USP14 | GRCh38.p7 | 18:163818 | GTACCCGATAGGTAG[-/T]TTTTTTTTTTTTTTA | 9097 |
rs570500217 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:159722 | ATGGCTCTTGAAATA[C/T]TCTAATACTTAAACA | 9097 |
rs570533343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:192614 | ATATGAGTTTGACAA[A/G]GGGAAAGAGCTTAAA | 9097 |
rs570627557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:200621 | TGCTAATAAGCCCAT[A/G]GATAAAACATACGGT | 9097 |
rs570650099 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213428 | CAAGTAGAAATGGGA[A/G]TTAGTTATACCAGTG | 9097 |
rs570679237 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:176276 | TTTTTATATAATCAT[A/C]TTTTGTTGAATGAAG | 9097 |
rs570712269 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214184 | TCGTGGCAGGCAGAA[C/T]AAACCATCATTTGTT | 9097 |
rs570738307 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:176737 | ATGAGTTTTTTGATT[C/G]ACTTGCATTCTTTTA | 9097 |
rs570773239 | snp | C/T | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:211819 | GGGCACAATCAAGTA[C/T]TTGTCCAGCCTATTG | 9097 |
rs570840450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:166073 | CTTTATAGATGCGTT[A/G]TAGACATTAACTCTT | 9097 |
rs570877710 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:177657 | TTTTTTTAAATCTCC[A/G]CTTCTGGTCCTACCT | 9097 |
rs570932469 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:194731 | AGGCCAGGGGTTTGA[G/T]ACCAGCCTGGCCAAC | 9097 |
rs571074082 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:179977 | ATAAACCTGCAAAAA[A/G]GGCAAGACTAGTATG | 9097 |
rs571127475 | in-del | -/TATTT | 0.00677013 | 0.0577861 | intron-variant | USP14 | GRCh38.p7 | 18:188675 | TTTTTTGGGGTATTT[-/TATTT]TATTTTATTTTATTT | 9097 |
rs571364950 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:162654 | GTGAATGATTCTTCA[A/G]TTAAACACATGGGGG | 9097 |
rs571470245 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:184708 | GGGAGGTCGAGTCTG[C/T]AGTGAGCCATCAGTG | 9097 |
rs571581090 | in-del | -/AA | | | intron-variant | USP14 | GRCh38.p7 | 18:173007 | TTTGTACTATGTTGT[-/AA]AAGAAATCTTCGCCT | 9097 |
rs571640307 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:174613 | TACTTTTCTTTCTTT[C/T]TTTTTTTTTTTTTAA | 9097 |
rs571694706 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:183856 | TCATATCATGCAACC[A/G]TATTCTCTTCCTTAT | 9097 |
rs571727968 | snp | A/G | 6.60262e-05 | 0.00574532 | synonymous-codon | USP14 | GRCh38.p7 | 18:204659 | CAAATTCAAGGATCT[A/G]GAAGATAAAAAAGTG | 9097 |
rs571733465 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP14 | GRCh38.p7 | 18:165242 | GTGAGCCACCACACC[C/T]GGCCTCTATTATTTT | 9097 |
rs571791294 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:196493 | CGCGCCACTGCACTC[C/T]AGCCTGGGCAACGGA | 9097 |
rs571791614 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:197148 | TTCCTTAAACCTTTC[A/C]AGTGCCCTCTTCCTG | 9097 |
rs571799435 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:194178 | GATTTTTGATATTAT[A/G]AACAGGTTTCTTTTG | 9097 |
rs571822109 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:204155 | CTATAAGCTATTGAA[C/G]TATATCACTATTACT | 9097 |
rs571847565 | in-del | -/ACTT | | | intron-variant | USP14 | GRCh38.p7 | 18:181820 | TTCTAGGTTACAAAG[-/ACTT]ACTTCTTTGTTGTTT | 9097 |
rs571895400 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:189898 | AAAGGCAGAACCCTT[A/C/G]TAGCACTCTAAAAAT | 9097 |
rs571972441 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP14 | GRCh38.p7 | 18:176909 | TTTTTTAAGGGCATT[A/G]TTTTAGTCTCTATTC | 9097 |
rs571975417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:190359 | GGTCATAAAAGGATT[C/T]ATATATTCAGTTTTA | 9097 |
rs572083942 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:186488 | CCAGGAGCAGTGGCT[A/C]ATGCTTGTAATCCCA | 9097 |
rs572135198 | in-del | -/CT | 0.0023933 | 0.0345097 | intron-variant | USP14 | GRCh38.p7 | 18:191363 | CAATTTAACACAATA[-/CT]CTCTGTGATTTCTTT | 9097 |
rs572211735 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:205159 | GGGGATTATAGGCAT[A/G]AGGCACCACACCTGG | 9097 |
rs572249710 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:192040 | TAAAGCTGAAAGTGA[A/G]TTTAGAAATCATTTA | 9097 |
rs572255698 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:159599 | TACAAAGCATGATAC[A/G]AATCAAGAGTATTGT | 9097 |
rs572294024 | snp | C/T | 1.64746e-05 | 0.00287002 | synonymous-codon | USP14 | GRCh38.p7 | 18:196713 | ACTGCAGTTTTTGCA[C/T]ATGGCTTTCCCACAG | 9097 |
rs572343414 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:160210 | TGGGGAGGCTGAGGC[A/T]GGAGAATCGCTTGAA | 9097 |
rs572386384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:178353 | TGTTATGGAGAGAGA[C/T]AATGCCACTAAATGT | 9097 |
rs572410929 | in-del | -/TTTTAATA | 0.0023933 | 0.0345097 | intron-variant | USP14 | GRCh38.p7 | 18:176908 | TTTTTTAAGGGCATT[-/TTTTAATA]GTTTTAGTCTCTATT | 9097 |
rs572411669 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:183264 | GCTTACTGATGAGAG[G/T]TCTGATATCAGTCTT | 9097 |
rs572415258 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:201389 | TAAACACTGAAGTGG[A/G]ACATGGATTATGTTG | 9097 |
rs572424554 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:193669 | CTCTGGACTTTTACT[C/G]TAAATGGAATTAAAT | 9097 |
rs572448787 | snp | A/T | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212245 | GATTTCTTTGGATGC[A/T]GAATGCAGTGATGTT | 9097 |
rs572458649 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | USP14 | GRCh38.p7 | 18:193375 | TAATACTGTTAAATC[-/T]TTGGGTTAGGTCAAT | 9097 |
rs572503684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:179319 | TAACTTACATATATT[C/T]AGCTAATATCTGTAA | 9097 |
rs572591929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:208432 | ATATCTTCAAAGAAT[C/T]GGCTTTGTTTCATGG | 9097 |
rs572754816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:196328 | GAGACCAGAGCCTGG[C/T]CAGCATGGTGAAACC | 9097 |
rs572835273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:182495 | TTTCTCTGAAGCGAA[C/T]AGTTGTCAGGTATTT | 9097 |
rs572874231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:183425 | CTGAGGACTCTTGTC[A/G]CAAACTCTAGGACAT | 9097 |
rs572966011 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:162376 | TTTTCTGTTAAATTT[A/T]AAAAAGAATAGCCAT | 9097 |
rs573012587 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:168000 | TAGAGTGCAATGGCG[C/T]GATCTCGGCTCGCTG | 9097 |
rs573142355 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157525 | AGAAGCGACTCCTTG[C/T]CCATTAAAGCTTTGT | 9097 |
rs573167467 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212781 | GGGAAAGGATAAAGC[A/G]TAGAATACCAGCCAG | 9097 |
rs573194783 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | USP14, LOC105371951 | GRCh38.p7 | 18:158289 | TCTGCCGCAGGGCTG[C/G]GCCGCGCCAGGACCA | 9097 |
rs573248756 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:164398 | CTGGTTCTGGAAAAC[C/T]GTTCATTTTTTTTTT | 9097 |
rs573342825 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:174933 | GGAATGTGCCACCAC[A/G]CCGGACTAATTTTTG | 9097 |
rs573377550 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:175494 | ATGCCTTTTCTATAT[A/C]ATTTCTTCCTCTCAT | 9097 |
rs573391158 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:191705 | TGTTTCACTCAGTAT[C/T]TAGCTTGGAGATCCA | 9097 |
rs573463552 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:190492 | AGCCAAGTTATTTAG[C/T]CAGTGGATTTAGAAA | 9097 |
rs573511394 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:160466 | AGTTAGAGGGTGCTG[G/T]GATCTGTGATCACGC | 9097 |
rs573526019 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:169916 | ATCGACAAATGTGTC[A/T]TCTGACAGCCTCACC | 9097 |
rs573535823 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:173170 | CTGGAGTGCAGTGGC[A/G]CGATCTCGGCTCACT | 9097 |
rs573542243 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:162290 | TCATATGGTAATTCT[A/G]TGTTTACTTTTATTC | 9097 |
rs573560991 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:206905 | AGTCCATGCCCTCAG[-/A]GATTTATACGTATGT | 9097 |
rs573588675 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:208903 | GGCGAGTGCCACCAT[A/G]CCTGGCTAATTTTTG | 9097 |
rs573590519 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:163669 | GTATTATAAAAACAT[C/T]GTTTTAAAACTCTTT | 9097 |
rs573619994 | in-del | -/CAG | | | intron-variant | USP14 | GRCh38.p7 | 18:208535 | TATAAATTTCCCTTT[-/CAG]CAGTGATTTCACTAT | 9097 |
rs573622927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:160900 | TTACACATTGCCTAC[A/G]ACATAAAGCCTTTAC | 9097 |
rs573639337 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:180571 | CGTACTCACTGGCAG[A/T]CACTCCTTTAACCCC | 9097 |
rs573650320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:167209 | ATCACTTGAACCTGG[A/G]AGGCGGAGATTGCAG | 9097 |
rs573680005 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:179240 | AAGGCACAGCTAGGG[G/T]TTTTTTTTTGTATTG | 9097 |
rs573681964 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:173363 | TGATCAGCCCGCCTT[A/G]GCCTCCCAAAGTGCT | 9097 |
rs573686424 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:198542 | TTTATACCTAAAAAA[A/C]TACAATAATGGAAAT | 9097 |
rs573715980 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP14 | GRCh38.p7 | 18:170214 | GAGGCTGAGGCAGGA[A/G]AATTGCTTGAGCCTG | 9097 |
rs573716505 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:191242 | AATTCAGGCATTATT[G/T]TGAATTATTGTGTAT | 9097 |
rs573747089 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:167994 | CCAGGCTAGAGTGCA[A/T]TGGCGCGATCTCGGC | 9097 |
rs573748524 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:196193 | GCCAGGCATGGTGGC[A/G]TGCTCCTGTAATCCC | 9097 |
rs573805980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:168388 | TCCCTTTTCAATATT[C/T]GTGACTTTCAGATTT | 9097 |
rs573828177 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:186827 | TGTGTAGCAGTGTAT[G/T]TGTTTTTTTATAACC | 9097 |
rs573882727 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:208531 | GTGATATAAATTTCC[C/T]TTTCAGCAGTGATTT | 9097 |
rs573938158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:180812 | CACGTTACAGCACAC[A/G]TAACACCTCATTCCT | 9097 |
rs573992002 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:173255 | TGGGACTACAGGTGC[A/C]TGCCACCACACCCGG | 9097 |
rs573994046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:166607 | CAAAGTGCTGGGATT[A/G]CAGGCGTGAGCCACT | 9097 |
rs574077704 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:176022 | ATTGATTGTCATATT[C/G]TACTGTTATTACCCT | 9097 |
rs574150632 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:187436 | AGTCATGTTCAATAC[A/G]CCTTTCTCCCTCTAA | 9097 |
rs574203189 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:171343 | CTTGTTAGAGGCTAA[G/T]GTAGCTAATGACTTT | 9097 |
rs574424143 | in-del | -/AAA | 0.00119737 | 0.0244387 | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:213929 | GACTTCATTTCTTTT[-/AAA]AAAGTTGGCAAACAA | 9097 |
rs574486820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:192996 | TGTCTTTTGTAAAAC[A/G]TCACCTCATTAAGCC | 9097 |
rs574544796 | snp | A/C | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:158017 | TATATAGAACGCAAT[A/C]AAATGAGGTGTGGGT | 9097 |
rs574569358 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:190920 | TTTATTGCTCTAATA[G/T]GGGAATTTTTTTTTG | 9097 |
rs574610841 | in-del | -/TCTT | | | intron-variant | USP14 | GRCh38.p7 | 18:176779 | TTTTTTACATTTAAA[-/TCTT]TAATTAATTGTTGTT | 9097 |
rs574634092 | in-del | -/ATTT | 0.00478085 | 0.0486577 | intron-variant | USP14 | GRCh38.p7 | 18:179542 | TTTTTAACACCTAGC[-/ATTT]ATTTAGTGCCATTCA | 9097 |
rs574683311 | snp | C/T | 3.30098e-05 | 0.00406249 | synonymous-codon | USP14 | GRCh38.p7 | 18:198124 | CTTCGGTGTTGAGTT[C/T]GAAACTACGTATCCT | 9097 |
rs574691439 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:205915 | TTTCATTGCTGATCA[A/G]TATTCCCTGGTGTGA | 9097 |
rs574764368 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:199025 | GTTGTTTCTAGAATT[G/T]TTGGTAGCCAAATGA | 9097 |
rs574801647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:185441 | ATTACAGGTGTGAGC[C/T]ACTGTGCCTGGCTGA | 9097 |
rs574841208 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:186301 | CATCTCTGCAATAAA[A/C]AAGAAATAGCTGAGT | 9097 |
rs574842462 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:189717 | CGATCTCTTGACCTC[A/G]TGATCCACCTGCCTC | 9097 |
rs574890594 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:193281 | TGTGTGTGAGGAGAA[A/G]TAGTAATCTTAAAGG | 9097 |
rs574893017 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:196299 | AAGTGAGCGGATCAT[A/G]AGGTCAGGAGTTGGA | 9097 |
rs574901496 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:186441 | AGCCTGGGCAATGCA[A/G]TGAGACCCTGCCTCT | 9097 |
rs574906603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:165117 | CCATGCGTGACAAAT[A/G]TTTGTATTTTTGGTA | 9097 |
rs575009366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:165634 | GAGGAAATTTTATAA[A/G]TGAGTGTCAAAGAGG | 9097 |
rs575047903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:207099 | CAGATGGTCTTGGAA[C/T]CTTTGTAGAGATTAA | 9097 |
rs575106925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:209572 | ATACAAATTGCAGGA[A/G]TTCTTGTTTTAGAGG | 9097 |
rs575189668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:203735 | CAGCCTCAACCTCCC[A/G]AGTAGCTGGGACTAC | 9097 |
rs575260579 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:188989 | TGGCCTTTGGGGTAT[G/T]TTAAATGTACTTATT | 9097 |
rs575363210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:167797 | CTGGGATTAACAGGT[A/G]TGAGTCACTGTGCCC | 9097 |
rs575380644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:168343 | TGTGTACATAAACGT[A/G]TTATCTGCAAATAAT | 9097 |
rs575426453 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:161652 | AAATGAATACTCAAC[A/G]TATTAATTGAACTGA | 9097 |
rs575431291 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:181293 | AATGATTTTCCAAAG[G/T]GACGGTACCATTTTA | 9097 |
rs575442081 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:162200 | ATAATGCTGCTGTAA[A/G]CATGGGTGTACAAAT | 9097 |
rs575564749 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:163073 | GAGCCACCACGCCCA[A/G]CCTGCTGAAGTCTCA | 9097 |
rs575679802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:169864 | TTTGTAATTGTTTTG[A/G]GGTGTCATGAATCAC | 9097 |
rs575715849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:160288 | CAGTCTGGGTGAAAA[A/G]AGCGAAACTGGGTCT | 9097 |
rs575778938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:205065 | ATTTTTGGTAGAGAC[A/G]GGGTTTTGCCATGTT | 9097 |
rs575844083 | snp | C/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:205495 | TTCAAGAAAGTTGGC[C/T]AGGCATGGTGGCTCA | 9097 |
rs575863825 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:167753 | ACTCCAGGGCTCAAG[C/T]GATCCTCCTGCCTTG | 9097 |
rs575915279 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:165836 | AGTTACCGTTCCATT[A/T]TAAAGCAGATAAAAG | 9097 |
rs575957019 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:174147 | ATGTCAGTCTGGGAC[A/G]TCTCAATATTGAGTC | 9097 |
rs575958724 | snp | A/G | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:172802 | ACTTCACAGACTGAT[A/G]TAAACATGATGTTTG | 9097 |
rs576012313 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:179376 | ATATAAGTATTTACT[A/G]TTACTATTTTATGAG | 9097 |
rs576014198 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:169292 | CTTGACTTTGGGAGG[C/T]GGAGGTTGCAGTGAG | 9097 |
rs576065137 | snp | C/G/T | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:209378 | AAGAACTTTGTGCTG[C/G/T]ATTCCTAGATAAGTT | 9097 |
rs576116838 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:191590 | TAATCCTTATCCTCT[C/G]CACCCCCTTCCAGCA | 9097 |
rs576180979 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:208486 | AGTTGTATTGATTTC[G/T]GCTCTTATTTCCTTT | 9097 |
rs576201511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:160873 | GTGGCCTTTATGACA[A/G]CCTTTCAGGAATTAC | 9097 |
rs576214568 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP14 | GRCh38.p7 | 18:173252 | AGCTGGGACTACAGG[C/T]GCCTGCCACCACACC | 9097 |
rs576216266 | in-del | -/T | 0.00835141 | 0.0640778 | intron-variant | USP14 | GRCh38.p7 | 18:185645 | ACTTAAATTATTTTC[-/T]TTTTTTTAGCTTTTT | 9097 |
rs576239400 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:200978 | GGCTGATTTTTGGTA[G/T]TTTTGATAGAGACAG | 9097 |
rs576241580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:208865 | ATTCTCATGCCTCAG[C/T]GTCCCGAGTAGCTGG | 9097 |
rs576261889 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:195637 | GAAGGTAAATTCTTA[C/G]TAGTTTTGGTTCTTA | 9097 |
rs576284092 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:185349 | TTTTTAGTAGAGACG[A/G]GTTTTGCTATATTGT | 9097 |
rs576299183 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:201934 | TGAGTAATTTGGCTT[C/T]GTTTCTCCACTGCTT | 9097 |
rs576323984 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:183161 | CTCTTATCCTTGGAT[A/G]ATAATATTGCTTGGA | 9097 |
rs576324924 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:164974 | TTTTTTGGGATTGAG[G/T]CTCCCTCTGTCACTC | 9097 |
rs576330960 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:195046 | AAGTTTTTTTTTTTT[-/C]CCTTCTTCAGGATTC | 9097 |
rs576336067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:188175 | TCTTTTTTCTTTTTT[C/T]CTCCTTGTCTTCTTC | 9097 |
rs576410531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:183523 | TAGATCTGTTTTTTA[A/G]TCTTCTAACTTTCCT | 9097 |
rs576442077 | in-del | -/CAT | 0.00119737 | 0.0244387 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213579 | CACTCACACCGAGGC[-/CAT]CATCATCTCAACATT | 9097 |
rs576507034 | in-del | -/AGTT | 0.00594009 | 0.0541734 | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214114 | CATAGACAGTTAGTT[-/AGTT]AGTTAGTTATGAGTG | 9097 |
rs576581713 | snp | A/G | 1.6679e-05 | 0.00288777 | intron-variant | USP14 | GRCh38.p7 | 18:163479 | GTCCAAATTTTCATC[A/G]CATTACTATTATTGT | 9097 |
rs576695171 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:187396 | GGATAGTTTGATCCA[A/T]ATTTTACATATCTTT | 9097 |
rs576709066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:201519 | GAGTCACGCTCTGTC[C/T]TATGATACCGAGGGG | 9097 |
rs576748458 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:191525 | TGCCTATCAAAGTAT[A/G]GAACATTTCTATCAT | 9097 |
rs576797334 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:203461 | ATATTATATTTTTCA[A/T]AAGATTCATATACAA | 9097 |
rs577014216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:197483 | ATTTTTTGGAAGATC[A/G]TATGTCTTATTTGGC | 9097 |
rs577035780 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | USP14 | GRCh38.p7 | 18:213757 | GGGAACAAGAAAAGT[C/T]GGTGGTACTGTCTTC | 9097 |
rs577049852 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:207998 | GAAGAGATTATGTAG[A/T]ATTGGTGTTAATTTT | 9097 |
rs577106236 | in-del | -/AT | 0.0023933 | 0.0345097 | intron-variant | USP14 | GRCh38.p7 | 18:162439 | TTTTAAATGATTTAG[-/AT]ATGTCTTTGGATTTT | 9097 |
rs577144688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:206206 | ATTCACTTTCTCTGC[A/G]TTCTCACCAGCATTT | 9097 |
rs577247908 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:169059 | TCTAGCCTGGGCAAC[A/C]GAGCGAGACTCCATC | 9097 |
rs577282582 | snp | C/T | 4.94515e-05 | 0.00497225 | missense | USP14 | GRCh38.p7 | 18:192883 | GGGAAATGGCTTCAG[C/T]GCAGTATATTACTGC | 9097 |
rs577350103 | in-del | -/TTAA | 0.00279162 | 0.0372561 | intron-variant | USP14 | GRCh38.p7 | 18:176782 | TTTACATTTAAATCT[-/TTAA]TTAATTGTTGTTGTG | 9097 |
rs577384604 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:164654 | AGATGGGGTTTCACC[A/G]TGTTGGCCAGTTTGG | 9097 |
rs577395565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:164557 | CTCCTGGGTTCAAGC[A/G]ATTCTTATGCCTCAG | 9097 |
rs577555763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:202649 | ACAGTATTTACACTC[A/G]GAGGAATCCACAACA | 9097 |
rs577596964 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | USP14, LOC105371951 | GRCh38.p7 | 18:158352 | GTGCGCAGGCGCGCA[C/T]CTGCTGCGGTGGATG | 9097 |
rs577618289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:203621 | TGGTTTCTTTCTTTT[C/T]TTTTTTGAGACGGAG | 9097 |
rs577618914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:195761 | TTGGGAGAGGTGACC[C/T]GCTATCCTGATCTTG | 9097 |
rs577627984 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:172167 | CGCTTAAGCCTAGGA[A/G]TTTGAGGTTACAGTG | 9097 |
rs577643087 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:162428 | TTTCTATATATTTTT[A/T]AATGATTTAGATATG | 9097 |
rs577677452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:196223 | CAGCTACTCGGGAGG[C/T]CCTTCTGTGTTCAAG | 9097 |
rs577686855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:161597 | TTAGGCTGTAAGTTT[A/G]TGGAGAGTCTTCCCA | 9097 |
rs577740848 | in-del | -/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213369 | TTATAAAAAGCTTGA[-/T]TTTTTTATTTGATCT | 9097 |
rs577826750 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:188513 | TCCCTCTGGCTTTTT[A/T]TTTTTTTTTTTTCCT | 9097 |
rs577847898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:167716 | GATGGGGGTGTCACT[A/G]TGTTGCCCAGGCTGG | 9097 |
rs577937562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:167275 | AACAGAGCGAGACTC[C/T]GTCTCCAAAAAAAGA | 9097 |
rs577988808 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:161028 | CACCTCCTGGTTTCA[A/G]GCGATTCTCCTGCCT | 9097 |
rs578162252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:204467 | TTTTATTTTCAACTG[C/T]ATCTGAATTATGAAA | 9097 |
rs578162410 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212566 | CTGAGATCACACCAC[C/T]GCACTCCAGCCTGGG | 9097 |
rs578203810 | snp | C/T | 8.25185e-05 | 0.0064228 | synonymous-codon | USP14 | GRCh38.p7 | 18:180331 | TGAACTCAAAGATGC[C/T]CTTAAAAGGTAAGAC | 9097 |
rs578234431 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP14 | GRCh38.p7 | 18:180986 | AGTATTTCATGGTTC[A/G]TTCATGTTACAGCAC | 9097 |
rs745355176 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:185060 | ACAGTATCACATGGC[C/T]GTATCTGTTGTATTG | 9097 |
rs745356186 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:170290 | GCCTGGCCAACAGAG[C/T]GAGACTCTGTCTCAA | 9097 |
rs745363361 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:161234 | TTCCCGGCCTCTTTA[C/T]GTATGATTTAGGATG | 9097 |
rs745376382 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:188835 | GGCACCCGCCACTAT[A/G]CCCAGCTAATTTTTT | 9097 |
rs745392885 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:163904 | CCTGTCTATGTGTCT[A/G]TGTGTTCTCATTATT | 9097 |
rs745402739 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:173340 | ATGGTCTCTATCTCC[C/T]GACCTCGTGATCAGC | 9097 |
rs745412753 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:196907 | CTCTTGCCTGGAGCC[A/G]CACAGTAGTCTTAAC | 9097 |
rs745419399 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:184039 | GAGAGTGCTCTTTTA[C/T]GTTTTGGAAAGAGTT | 9097 |
rs745467673 | snp | A/T | 1.66754e-05 | 0.00288746 | missense | USP14 | GRCh38.p7 | 18:209975 | TTTCTCCTCAGAGTG[A/T]CAAAAAGAGTAGTCC | 9097 |
rs745561693 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:195995 | TTTTTTCTTATTGAG[A/C]GTCCAACAATTGTCA | 9097 |
rs745589233 | snp | C/T | 1.65056e-05 | 0.00287272 | intron-variant | USP14 | GRCh38.p7 | 18:204701 | AAATACAGTAGGTTC[C/T]TACTGCTGACTTTAT | 9097 |
rs745608045 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:191754 | AGATCAGTAATTCTG[A/G]TTGCTCCACAATCTT | 9097 |
rs745698707 | snp | C/T | 3.37018e-05 | 0.00410485 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:211291 | GAACAGTAATCTTCA[C/T]TTTAGTATTTATGCT | 9097 |
rs745726337 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:205794 | TCTAAAAAAAAATTA[C/T]ACAAACGAAATAAAA | 9097 |
rs745734301 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:190841 | TTCTAAGTTTTTCTT[C/T]ATAAACTTCAGTGTT | 9097 |
rs745785283 | snp | A/G | 1.67492e-05 | 0.00289384 | synonymous-codon | USP14 | GRCh38.p7 | 18:163348 | ATTTGAAGGTGTAGA[A/G]TTGAATACAGATGAA | 9097 |
rs745796771 | in-del | -/G | | | intron-variant | USP14 | GRCh38.p7 | 18:174480 | CATGTTGGTCAGGCT[-/G]GTCTCAAACTCCTGA | 9097 |
rs745840454 | snp | C/G | 0.00015178 | 0.00871015 | intron-variant | USP14 | GRCh38.p7 | 18:158747 | CTCGCGCGCAGCACA[C/G]CGGACCGGCGCTAGG | 9097 |
rs745887432 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:202467 | TCATTGGTGCTGATT[A/G]GCTTTTATGCATAAA | 9097 |
rs745936843 | in-del | -/A | | | intron-variant | USP14 | GRCh38.p7 | 18:204992 | TGATCCTCCCACCTC[-/A]CCCTCCCAAGTAGCT | 9097 |
rs745973885 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:191808 | TTTTTTAAATTTTGA[C/T]TTTAGTCACTCTAAT | 9097 |
rs745982608 | snp | C/G | 1.70194e-05 | 0.00291709 | intron-variant, missense | USP14 | GRCh38.p7 | 18:179017 | GTAGAAGACATGACA[C/G]AAGAACAGTTAGCAT | 9097 |
rs746015959 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:201266 | TGTCTCCTCTAACCA[C/T]GACCAATAAAGAGAA | 9097 |
rs746038140 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:168340 | TTCTGTGTACATAAA[C/T]GTGTTATCTGCAAAT | 9097 |
rs746038298 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:178061 | GTCTCCCTCTGTCGC[A/G]CAGGCTGGAATGCAA | 9097 |
rs746091140 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:167456 | TCCTTATTTATTTAG[A/G]TCTCTGTTTTTCTCT | 9097 |
rs746095194 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:182650 | TTTGATGGGAAATGT[A/G]GGCTGCTATGAGAAC | 9097 |
rs746190496 | snp | C/G | | | missense | USP14 | GRCh38.p7 | 18:180320 | CGTTCTGTGCCTGAA[C/G]TCAAAGATGCCCTTA | 9097 |
rs746213004 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:162788 | ATCAATCTACTTCTC[G/T]GAAGTCTCAGTTTCT | 9097 |
rs746263779 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:174197 | TAAACCTTTCCTTTA[C/T]TTAAATGTTCAATGT | 9097 |
rs746272153 | snp | G/T | | | missense | USP14 | GRCh38.p7 | 18:210016 | GTTAAGTATGAACCC[G/T]TTTCTTTTGCTGATG | 9097 |
rs746272562 | in-del | -/T | 1.83152e-05 | 0.0030261 | intron-variant | USP14 | GRCh38.p7 | 18:178917 | TTTTCATGAAATTAC[-/T]TTTTTTTAAAAACAG | 9097 |
rs746302739 | snp | A/T | 1.66477e-05 | 0.00288506 | intron-variant | USP14 | GRCh38.p7 | 18:166865 | ATGCAGTAACCTCAT[A/T]ATGATACCAAAATAC | 9097 |
rs746309577 | snp | C/T | 1.65666e-05 | 0.00287802 | intron-variant | USP14 | GRCh38.p7 | 18:203047 | ACCAAATAATTAAAA[C/T]TTGTATGGTATTTTG | 9097 |
rs746397323 | in-del | -/A | 4.97888e-05 | 0.00498918 | intron-variant | USP14 | GRCh38.p7 | 18:197704 | TTAAAGAGGTAATTG[-/A]AATATATTTGTGATT | 9097 |
rs746405458 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:189552 | CAGTGGCACAATCTC[A/G]GCTCACTGCAGCCTC | 9097 |
rs746415969 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:173497 | GCTCACCGCAACCTC[C/T]GTCTCCCAGGTTCAA | 9097 |
rs746426411 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:201536 | ATGATACCGAGGGGA[A/G]AGTTTTGAGCCAGTG | 9097 |
rs746439795 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:205971 | CACCTATTGAAGAAC[A/G]CCTGGGTTGTTTCTA | 9097 |
rs746490993 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:205169 | GGCATGAGGCACCAC[A/C]CCTGGCCTTTAGGTG | 9097 |
rs746494933 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:173181 | TGGCACGATCTCGGC[C/T]CACTGCAAGCTCCAC | 9097 |
rs746527769 | snp | C/T | 0.000108419 | 0.0073619 | intron-variant | USP14 | GRCh38.p7 | 18:158727 | CCGGTGAGCCCTGTC[C/T]TGGCCTCGCGCGCAG | 9097 |
rs746546479 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:204531 | TATCTTTATAAATGT[G/T]TTTACACATGTTTTT | 9097 |
rs746577676 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:172271 | AGAAAAATGGAGCTT[A/G]AAATTGTGACTGAAT | 9097 |
rs746602009 | snp | G/T | 2.62836e-05 | 0.00362507 | intron-variant | USP14 | GRCh38.p7 | 18:204542 | ATGTGTTTACACATG[G/T]TTTTTGTTTGTTTGT | 9097 |
rs746619283 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:190995 | TGATAATTCATTAGT[A/G]TATCTTTGCCATAAA | 9097 |
rs746704357 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:185233 | GGTGCGATCTCAGCT[A/C]ACTGCAGCCTCTGCC | 9097 |
rs746722931 | snp | A/G | 2.82458e-05 | 0.00375794 | splice-acceptor-variant | USP14 | GRCh38.p7 | 18:163307 | GTGATTTTGTTTGCA[A/G]TTACTGTAAAATGGG | 9097 |
rs746859546 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:193066 | TATTTTATCGTCCAG[A/C]TTATAAATCAATGAT | 9097 |
rs746881876 | snp | A/T | 3.31862e-05 | 0.00407333 | intron-variant | USP14 | GRCh38.p7 | 18:197700 | TCTGTTAAAGAGGTA[A/T]TTGAAATATATTTGT | 9097 |
rs747006243 | snp | C/T | 3.37878e-05 | 0.00411008 | intron-variant | USP14 | GRCh38.p7 | 18:197577 | TTTGTAGATCATTCA[C/T]TGCCAGGATTACTTA | 9097 |
rs747012478 | snp | A/G | 1.67849e-05 | 0.00289692 | missense | USP14 | GRCh38.p7 | 18:211136 | CCTGTTATTTAGATG[A/G]ATGGATTAAGTTTGA | 9097 |
rs747071890 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:190413 | AAAACGGAGGTACCA[A/G]TTCATATTTTCATTA | 9097 |
rs747138059 | snp | A/C | 2.17621e-05 | 0.00329857 | intron-variant | USP14 | GRCh38.p7 | 18:199367 | AATTCCATGTTTGCG[A/C]GTAAGCCAAAGTCAT | 9097 |
rs747154426 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:204229 | TTTATTCCAGTTTGG[C/G]AGGTCCATTATTTTC | 9097 |
rs747187663 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:156767 | TATAAAAGTTATGTT[G/T]CTACTATACTGTAGT | 9097 |
rs747217352 | snp | C/T | 1.68442e-05 | 0.00290204 | intron-variant, synonymous-codon | USP14 | GRCh38.p7 | 18:179001 | AGCCAAAACTGTCTT[C/T]GTAGAAGACATGACA | 9097 |
rs747217961 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | USP14, LOC105371951 | GRCh38.p7 | 18:158170 | TCGCCCAGGCTGGAG[C/T]GCGGTGGCACGATCA | 9097 |
rs747235511 | in-del | -/A | | | intron-variant | USP14 | GRCh38.p7 | 18:169360 | GCAAGACTCTACCTC[-/A]AAAAAAAAAAAAAAA | 9097 |
rs747268614 | snp | A/C | 1.65979e-05 | 0.00288074 | intron-variant | USP14 | GRCh38.p7 | 18:166853 | ACGTTTATTATAATG[A/C]AGTAACCTCATTATG | 9097 |
rs747336682 | in-del | -/A | | | intron-variant | USP14 | GRCh38.p7 | 18:169363 | AAGACTCTACCTCAA[-/A]AAAAAAAAAAAAAAA | 9097 |
rs747384235 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:164241 | TAATTTTCTGTAATG[A/G]GGTTGGAAAATTTTA | 9097 |
rs747397089 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:200359 | AAACCAGGACACTTT[G/T]GTGGAGAGTGAATGA | 9097 |
rs747405347 | snp | A/G | 5.0145e-05 | 0.00500699 | intron-variant | USP14 | GRCh38.p7 | 18:196591 | ACAGTCGCGTGTATT[A/G]AATATGTGACTGTTT | 9097 |
rs747410834 | snp | A/G | 9.20988e-05 | 0.00678535 | intron-variant | USP14 | GRCh38.p7 | 18:199191 | CATATTCCTTATCTT[A/G]GTTTACAAAGCATGA | 9097 |
rs747440474 | snp | C/T | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213480 | ATTTTAGAATTCAGC[C/T]TTGCCTGTAAGGTCT | 9097 |
rs747472995 | in-del | -/AAG | 4.97872e-05 | 0.0049891 | cds-indel | USP14 | GRCh38.p7 | 18:210004 | CCCCAGAAAGAAGTT[-/AAG]TATGAACCCTTTTCT | 9097 |
rs747552107 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:176077 | CTTTTTCGTTTTCCT[C/T]TCTAGTATTGGCAAA | 9097 |
rs747557874 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:166826 | TAAAAAATGTAAGTA[-/T]TTATCTTATGAACGT | 9097 |
rs747593300 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:209669 | TCCTTTTCTGCCCTA[A/G]AGCACTGTTTAACTG | 9097 |
rs747610964 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:161249 | TGTATGATTTAGGAT[A/G]ACTTATCTTCCATAA | 9097 |
rs747637458 | snp | A/T | 1.69172e-05 | 0.00290832 | intron-variant | USP14 | GRCh38.p7 | 18:197569 | GGAAGAACTTTGTAG[A/T]TCATTCACTGCCAGG | 9097 |
rs747648298 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:207442 | TCAGCACTTTGGGAG[A/G]CCAAGGTGGGCAGAT | 9097 |
rs747670549 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:209886 | CACTGTAGACAGTAA[A/G]TATTTATGAAATTGA | 9097 |
rs747748142 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:159996 | AGTACTATTTCATAA[A/G]ATTTAGTAGAAAATT | 9097 |
rs747809831 | in-del | -/A | | | intron-variant | USP14 | GRCh38.p7 | 18:182733 | GAGTAACTGGTATTT[-/A]AACAGTTAGGTGTTA | 9097 |
rs747826208 | snp | A/C | 0.000100528 | 0.00708899 | intron-variant | USP14 | GRCh38.p7 | 18:158721 | TCTACTCCGGTGAGC[A/C]CTGTCCTGGCCTCGC | 9097 |
rs748030233 | snp | A/G | 1.64944e-05 | 0.00287175 | missense | USP14 | GRCh38.p7 | 18:210427 | TATGACTTACAAGCA[A/G]TACTAACACACCAGG | 9097 |
rs748053649 | snp | C/G | 1.65285e-05 | 0.00287471 | missense | USP14 | GRCh38.p7 | 18:196639 | CTTTGTCTTTAAGCC[C/G]TTAGAGATTTGTTTG | 9097 |
rs748118033 | in-del | -/TTG | | | intron-variant | USP14 | GRCh38.p7 | 18:174284 | TTTTTTTTTTTTTTT[-/TTG]AGACAGTCTTGCTCT | 9097 |
rs748118568 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:194256 | TAGACTTACTTGTTG[A/C]AATGAAGTTTTTAGT | 9097 |
rs748172003 | snp | A/T | 3.32425e-05 | 0.00407678 | missense | USP14 | GRCh38.p7 | 18:210022 | TATGAACCCTTTTCT[A/T]TTGCTGATGGTAAGT | 9097 |
rs748217974 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:176115 | TTGTCTGTTTCCTCT[A/G]TCATCAAGCCAGAGT | 9097 |
rs748228969 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:164353 | TTTGTATGTTGAAAT[G/T]CAAAGCACTTCAGCA | 9097 |
rs748257782 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:172513 | CTGTGGATAAAATGC[C/T]ATTAAACAGCACCGC | 9097 |
rs748309092 | in-del | -/T | 1.99436e-05 | 0.00315775 | intron-variant | USP14 | GRCh38.p7 | 18:198031 | AAGTTGGAATTTTTA[-/T]TTTTAATTTTTGCAG | 9097 |
rs748315721 | snp | C/T | 2.02895e-05 | 0.00318502 | intron-variant | USP14 | GRCh38.p7 | 18:199359 | TGTTTGTGAATTCCA[C/T]GTTTGCGAGTAAGCC | 9097 |
rs748351082 | in-del | -/TGTA | 1.68916e-05 | 0.00290612 | intron-variant | USP14 | GRCh38.p7 | 18:210063 | TTTTAATTGAGTTAT[-/TGTA]TGTGGGTCTTTTTAA | 9097 |
rs748395632 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:190197 | ATTCTTCTGTTGATG[A/G]ATATTTGGTTTATGT | 9097 |
rs748432151 | snp | C/T | 2.23516e-05 | 0.00334295 | intron-variant | USP14 | GRCh38.p7 | 18:199168 | ATAACAAATTGAATA[C/T]CCGTTGGCATATTCC | 9097 |
rs748487893 | snp | A/C | 1.65056e-05 | 0.00287272 | missense | USP14 | GRCh38.p7 | 18:204669 | GATCTAGAAGATAAA[A/C]AAGTGAATCAGCAGC | 9097 |
rs748567095 | in-del | -/ACA | | | intron-variant | USP14 | GRCh38.p7 | 18:206843 | AGGCAGAGGTTGTAG[-/ACA]TGAGCTGAGATCACG | 9097 |
rs748579348 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:185271 | TTGAGCAATTCTTCT[A/G]TCTCAGCCTCCCAAG | 9097 |
rs748639162 | snp | A/G | 1.65102e-05 | 0.00287312 | intron-variant | USP14 | GRCh38.p7 | 18:192806 | GTGTTAGAATGAATT[A/G]AATTCTATTGTTTAA | 9097 |
rs748670092 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:165791 | TATGTTTAGCAGTCA[C/T]AGACCTTAAATTGAG | 9097 |
rs748746064 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:195806 | CAATTACATTATGCC[C/T]GTTTGTCCCTAAACA | 9097 |
rs748753797 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:182948 | AGAAGTGTGGACTTC[A/G]TGTTGTGGGCGAAGA | 9097 |
rs748814068 | snp | C/T | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212751 | TCTTTGTTCCAGGAC[C/T]CTTGACTGATGCTAG | 9097 |
rs748834034 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:185846 | CCTCAGGCATGCACC[A/G]CTATGCCCAGCTGAT | 9097 |
rs748876583 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:194431 | CTTGATTTTTTAACT[A/T]TTTGTTTTGAAATAC | 9097 |
rs748883650 | snp | C/T | 1.65143e-05 | 0.00287348 | intron-variant | USP14 | GRCh38.p7 | 18:196797 | GTATTTTTCATTCTG[C/T]AAATGTAAAACTTAG | 9097 |
rs748889814 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:162700 | TTTTGGGAAATATTT[C/T]AATATGATCATATTG | 9097 |
rs748931275 | in-del | -/TAA | 0.00321005 | 0.0399339 | intron-variant | USP14 | GRCh38.p7 | 18:210356 | TGTCTATTCATTGTC[-/TAA]TATTAATGGATTTAC | 9097 |
rs748945175 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:161409 | TCTTCTGTCCTCTCC[C/T]AGTCTCTGACTAACA | 9097 |
rs748947108 | in-del | -/CTTTG | | | intron-variant | USP14 | GRCh38.p7 | 18:176209 | TCGTTTATTTTTTCT[-/CTTTG]CTTTCTTTCTTTCTA | 9097 |
rs749008423 | snp | A/T | 3.33356e-05 | 0.00408248 | intron-variant | USP14 | GRCh38.p7 | 18:196610 | ATGTGACTGTTTTAC[A/T]AAGGCAATGTTTGCT | 9097 |
rs749047785 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:172108 | TTGGGCATGGTGGTG[G/T]ATACCTGTAGTCCTA | 9097 |
rs749060033 | snp | C/T | 1.65696e-05 | 0.00287828 | synonymous-codon | USP14 | GRCh38.p7 | 18:163360 | AGAATTGAATACAGA[C/T]GAACCTCCAATGGTA | 9097 |
rs749105018 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:156964 | CCAGTTACTCAGGAG[A/G]CTGAGGTGAGAGGAT | 9097 |
rs749138544 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:203003 | AAATATTTCCAGTTA[A/G]TTAATTTTATCCAGT | 9097 |
rs749286111 | in-del | -/ACTA | | | intron-variant | USP14 | GRCh38.p7 | 18:194485 | AAGAATTCACCAGTT[-/ACTA]ACTTTTAGTCGCATT | 9097 |
rs749360347 | in-del | -/T | 5.02778e-05 | 0.00501362 | intron-variant | USP14 | GRCh38.p7 | 18:210506 | AGGTAAAGGGTATTC[-/T]TTTTTTCAACTGTTC | 9097 |
rs749364762 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:174671 | GTGCAGTGGCACAAT[A/C]ATAGCTCGCTGCAGC | 9097 |
rs749374096 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:165956 | CCTATGAGGGGAAAG[G/T]CCTAGCTGTAGTTAG | 9097 |
rs749381492 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:167289 | CCGTCTCCAAAAAAA[C/G]AGTCTTGAAATAAGA | 9097 |
rs749404729 | snp | A/G | 3.29913e-05 | 0.00406135 | synonymous-codon | USP14 | GRCh38.p7 | 18:198097 | TAAAAAGAAAAGTTT[A/G]ATCGATCAGTTCTTC | 9097 |
rs749433690 | in-del | -/TTGC | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214005 | ATAGATAGATGATGA[-/TTGC]TTGATTGATGATTGA | 9097 |
rs749464624 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:173372 | CGCCTTGGCCTCCCA[A/G]AGTGCTGGGATTACA | 9097 |
rs749506768 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:177722 | AAGATACTGAGTAAG[A/G]GAGTAAGATGTTATT | 9097 |
rs749559029 | in-del | -/ATCCAGCCTCA | | | intron-variant | USP14 | GRCh38.p7 | 18:203945 | ATCCCTTGATTTAGG[-/ATCCAGCCTCA]GAATCTGACTGTTTT | 9097 |
rs749645472 | snp | A/G | 1.6552e-05 | 0.00287676 | intron-variant | USP14 | GRCh38.p7 | 18:203065 | GTATGGTATTTTGAT[A/G]TAATGGGATTTCTTT | 9097 |
rs749671382 | in-del | -/TG | | | intron-variant | USP14 | GRCh38.p7 | 18:180083 | TGGGGGAAATAAAAC[-/TG]TGTTTCTTTAGCGTG | 9097 |
rs749757792 | snp | A/G | 9.89544e-05 | 0.00703331 | missense | USP14 | GRCh38.p7 | 18:180306 | CAGTTCAGTGTATTC[A/G]TTCTGTGCCTGAACT | 9097 |
rs749763559 | in-del | -/TATTT | | | intron-variant | USP14 | GRCh38.p7 | 18:160917 | CATAAAGCCTTTACG[-/TATTT]TATTTTATTTTTTTT | 9097 |
rs749878203 | snp | C/T | 1.76936e-05 | 0.00297431 | intron-variant, synonymous-codon | USP14 | GRCh38.p7 | 18:179037 | ACAGTTAGCATCTGC[C/T]GTAAGACACACCAGA | 9097 |
rs749938094 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:198324 | CTCACTGCAACCTCC[A/T]CCTCCTGGGTTCAAA | 9097 |
rs749978967 | snp | A/G | 1.69083e-05 | 0.00290755 | missense | USP14 | GRCh38.p7 | 18:199287 | TTTATCAATCAGGAA[A/G]TCAAGTATCTTTTTA | 9097 |
rs749984680 | snp | C/T | 3.30186e-05 | 0.00406303 | missense | USP14 | GRCh38.p7 | 18:163446 | TGGTGAAAGGAGGAA[C/T]GCTAAAGGTAAAATG | 9097 |
rs750055473 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:176956 | TAGCTATTATCCTGG[A/G]TATAAATTTGCTGCA | 9097 |
rs750152031 | snp | A/T | 1.65026e-05 | 0.00287246 | missense | USP14 | GRCh38.p7 | 18:166788 | TGTCTTTGAAACAGG[A/T]TGATGATTGGGGAAA | 9097 |
rs750157273 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:202693 | GATGCCTTGTAAGAA[C/T]TGAACAGTATCTAAA | 9097 |
rs750192011 | snp | A/C | 1.6512e-05 | 0.00287328 | intron-variant | USP14 | GRCh38.p7 | 18:192910 | CTGCAGGTTTGTATA[A/C]TAAATATACTACTTT | 9097 |
rs750273379 | in-del | -/TAGT | | | intron-variant | USP14 | GRCh38.p7 | 18:161548 | TTTGTAATACTTACA[-/TAGT]TAATTACTCTAGCCT | 9097 |
rs750277596 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:187305 | TTGAGGTCTGATTTT[C/T]GATATGTGTTTGTAT | 9097 |
rs750498507 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:184520 | GTACTTTGGGAGGCC[A/G]AGGCAGGTATCTCAC | 9097 |
rs750594461 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:183541 | TTCTAACTTTCCTCC[A/G]TGTTTTAAATTTTTA | 9097 |
rs750645814 | snp | A/T | 1.67478e-05 | 0.00289372 | intron-variant | USP14 | GRCh38.p7 | 18:180388 | TCACATTTGGATGAG[A/T]AGTATTGTTTTGTTT | 9097 |
rs750652268 | snp | A/G | 1.64923e-05 | 0.00287156 | missense | USP14 | GRCh38.p7 | 18:180290 | TGTTACATGAATGCC[A/G]CAGTTCAGTGTATTC | 9097 |
rs750662148 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:195424 | GATGATAGGTGACAT[C/T]TCACATCTTGGGTAT | 9097 |
rs750713987 | snp | C/G | 3.31274e-05 | 0.00406972 | missense | USP14 | GRCh38.p7 | 18:204623 | ACCAGAACTTCAAGA[C/G]AAAATGGTGTCTTTT | 9097 |
rs750755027 | in-del | -/G | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214228 | AAAGCACGAATAAGT[-/G]AGAACAGAGCAGTCA | 9097 |
rs750795127 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:175688 | ATTCTTTTTTATCTG[G/T]TTTTGCTATCAGTGT | 9097 |
rs750801023 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:206034 | ACATTCGTGTACAGG[-/T]TTTAATGTAAACGTA | 9097 |
rs750820867 | snp | A/G | 1.65102e-05 | 0.00287312 | missense | USP14 | GRCh38.p7 | 18:197649 | ATACAAATGATGCGA[A/G]TATTGCAACAGAAAT | 9097 |
rs750865293 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:190142 | TTCATGCTATATAGT[A/G]TAGTATTCCGTTGTG | 9097 |
rs750929486 | snp | A/G | 5.95575e-05 | 0.00545667 | intron-variant | USP14 | GRCh38.p7 | 18:163288 | TTTTTTAATTAAAAA[A/G]ATTGTGATTTTGTTT | 9097 |
rs750981744 | snp | C/T | 8.98513e-05 | 0.00670206 | utr-variant-5-prime | USP14 | GRCh38.p7 | 18:158695 | CCTCCCGCCGCGCCC[C/T]GCCATGCCGCTCTAC | 9097 |
rs751038354 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:193680 | TACTCTAAATGGAAT[G/T]AAATAATATGTAGTC | 9097 |
rs751165755 | snp | A/G | 1.64917e-05 | 0.00287151 | synonymous-codon | USP14 | GRCh38.p7 | 18:163435 | ACAGAAAGTTATGGT[A/G]AAAGGAGGAACGCTA | 9097 |
rs751236247 | in-del | -/A | 1.6517e-05 | 0.00287372 | intron-variant | USP14 | GRCh38.p7 | 18:166758 | TGTACAGTGGTGGTT[-/A]AAATGTCTTTTGTTT | 9097 |
rs751291820 | in-del | -/T | 1.6512e-05 | 0.00287328 | intron-variant | USP14 | GRCh38.p7 | 18:192910 | TGCAGGTTTGTATAC[-/T]TAAATATACTACTTT | 9097 |
rs751307483 | snp | A/C | 1.65222e-05 | 0.00287417 | intron-variant | USP14 | GRCh38.p7 | 18:198155 | TATGAGCCAAGATAT[A/C]GACTATACTCATACC | 9097 |
rs751357611 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:210643 | TTATGAGGTTTGCCT[C/T]TCTTAATACTTACTG | 9097 |
rs751372886 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:162107 | ATAATATTCCGTTGT[A/G]TGTATATACCACATT | 9097 |
rs751413511 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:205390 | CCACAAAGATCTTGC[A/C]TTATTGCCACAGGGC | 9097 |
rs751597651 | snp | C/T | 0.000203666 | 0.0100892 | utr-variant-5-prime, downstream-variant-500B | USP14, LOC105371951 | GRCh38.p7 | 18:158666 | TCGTCAGGCCCAGCT[C/T]TCCTGCGCCGCCGCC | 9097 |
rs751603213 | in-del | -/C | | | intron-variant | USP14 | GRCh38.p7 | 18:186841 | TGTGTTTTTTTATAA[-/C]CAATTCAAACAGTCT | 9097 |
rs751608843 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157790 | GATATAATAGTATTT[A/T]AAAAGTTCAAAATAT | 9097 |
rs751636273 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:187415 | TTACATATCTTTGAA[C/T]TTCATAGTCATGTTC | 9097 |
rs751730074 | in-del | -/TATT | | | intron-variant | USP14 | GRCh38.p7 | 18:162288 | ATCATATGGTAATTC[-/TATT]TATGTTTACTTTTAT | 9097 |
rs751760709 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:171514 | ATATTTTAAGGCCAC[C/G]ATTGAGACTTCCTGC | 9097 |
rs751793598 | snp | C/G | 1.66454e-05 | 0.00288486 | intron-variant | USP14 | GRCh38.p7 | 18:203203 | AAGGTTAGTAATGAA[C/G]TTTACTTTGTATAAG | 9097 |
rs752033751 | in-del | -/TTGT | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214079 | CCTTAGCTTTGCTGT[-/TTGT]TGTTATAGTGTAGCT | 9097 |
rs752049021 | snp | A/G | 1.6534e-05 | 0.00287519 | missense | USP14 | GRCh38.p7 | 18:197622 | ACATTACAGGATGCT[A/G]ATGAATGTTGGATAC | 9097 |
rs752100111 | snp | A/G | 0.000108761 | 0.0073735 | intron-variant | USP14 | GRCh38.p7 | 18:211088 | GTGGAACTCTGAGAC[A/G]AATCCTGCATAACAT | 9097 |
rs752108484 | snp | A/G | 3.29538e-05 | 0.00405904 | missense | USP14 | GRCh38.p7 | 18:196754 | AAGGTGAACAAGGAC[A/G]GTATCTTCAACAGGT | 9097 |
rs752134871 | in-del | -/AGATTAGATAGATAGAT | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:213967 | TGTAATGGACAAGAT[-/AGATTAGATAGATAGAT]AGATAGATTAGATAG | 9097 |
rs752202394 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:173844 | TTTCCATTCTTCCTC[A/C]GTGCCTTTGTTGAAA | 9097 |
rs752274287 | snp | C/T | 1.72326e-05 | 0.0029353 | intron-variant | USP14 | GRCh38.p7 | 18:211119 | TAATTCATCTTCTTG[C/T]CCCTGTTATTTAGAT | 9097 |
rs752321778 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:202040 | TAAAAAATCAGACTT[C/T]AAAATTATACAAGTG | 9097 |
rs752322220 | in-del | -/AA | 3.33678e-05 | 0.00408446 | intron-variant | USP14 | GRCh38.p7 | 18:196609 | ATGTGACTGTTTTAC[-/AA]TAAGGCAATGTTTGC | 9097 |
rs752380018 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:187863 | TTACCCTGAAAACAC[A/G]TTTTAGTTATGATGA | 9097 |
rs752421927 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:183647 | TTTCACTGCTTACTT[A/T]TCATGACCTTCTGTT | 9097 |
rs752438772 | snp | A/C/G | 4.95678e-05 | 0.00497814 | missense | USP14 | GRCh38.p7 | 18:197679 | TTGGAAGCAATAGAG[A/C/G]ATGATTCTGTTAAAG | 9097 |
rs752441858 | snp | C/T | 1.65075e-05 | 0.00287289 | missense | USP14 | GRCh38.p7 | 18:211246 | CTACTCTATGGGCCT[C/T]GCAGAGTTGAAATAA | 9097 |
rs752523355 | snp | A/G | 1.65395e-05 | 0.00287567 | intron-variant | USP14 | GRCh38.p7 | 18:202972 | AGTCCTTTCGAAGCC[A/G]AATTCCGCTTCACTG | 9097 |
rs752525633 | snp | C/T | | | synonymous-codon | USP14 | GRCh38.p7 | 18:196719 | GTTTTTGCACATGGC[C/T]TTCCCACAGTTTGCC | 9097 |
rs752590484 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:180613 | CTAGCCCTAGCCAAC[C/G]GTTCATCTACTTTCT | 9097 |
rs752623450 | snp | C/T | 1.67674e-05 | 0.00289541 | intron-variant | USP14 | GRCh38.p7 | 18:180225 | CCTTTTTTTTTTTTT[C/T]TTCCAACTAGATGGA | 9097 |
rs752678365 | snp | A/C | 1.7107e-05 | 0.00292459 | intron-variant | USP14 | GRCh38.p7 | 18:178929 | TTACTTTTTTTAAAA[A/C]CAGGGAATGACTCTA | 9097 |
rs752682677 | snp | A/G | 1.6498e-05 | 0.00287206 | intron-variant | USP14 | GRCh38.p7 | 18:203083 | ATGGGATTTCTTTAC[A/G]TTTTGTCTCCTCAGT | 9097 |
rs752694169 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:162306 | TGTTTACTTTTATTC[C/G]CCCCAGCAGTGTACA | 9097 |
rs752703642 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:211120 | AATTCATCTTCTTGT[C/G]CCTGTTATTTAGATG | 9097 |
rs752722339 | snp | A/G | 1.64743e-05 | 0.00287 | missense | USP14 | GRCh38.p7 | 18:196714 | CTGCAGTTTTTGCAC[A/G]TGGCTTTCCCACAGT | 9097 |
rs752801702 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:166024 | AAAAATTCTTGATTT[G/T]TATTCAACATATTGA | 9097 |
rs752811522 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:207403 | TTAAAAAGTATTACT[A/G]TCTTAATAGTATTAA | 9097 |
rs752835633 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:203343 | ATTCTTAACTCAGAA[C/T]GTATATTAGAATTAT | 9097 |
rs752923045 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:159598 | TTACAAAGCATGATA[A/C]GAATCAAGAGTATTG | 9097 |
rs752936075 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:205670 | CCGGTAGTTCTAGCT[A/G]CTTGGGAGGCTGAGA | 9097 |
rs752974470 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:172844 | GGAAAATTTTTGTGT[A/G]ACTTGCTTTATTGCG | 9097 |
rs753045889 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:200873 | GTGGCACAATCTCGG[C/T]TCACTGCAACCTCTG | 9097 |
rs753081887 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:168215 | ACAGGCGTGAGCCAC[C/T]GCACCCGGCCAAAAT | 9097 |
rs753117656 | snp | A/C/G | 3.30089e-05 | 0.00406246 | intron-variant | USP14 | GRCh38.p7 | 18:166781 | TTTTGTTTGTCTTTG[A/C/G]AACAGGATGATGATT | 9097 |
rs753133147 | snp | A/G | 1.68869e-05 | 0.00290571 | intron-variant | USP14 | GRCh38.p7 | 18:210335 | TACTTAGCTTGAGAA[A/G]GCACATGTCTATTCA | 9097 |
rs753151678 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:179674 | CTCACTGTAACCTCA[A/G]CTTCCTGGGTTCAAG | 9097 |
rs753170890 | in-del | -/ATC | | | cds-indel | USP14 | GRCh38.p7 | 18:212176 | TTAAAAATATTTGTT[-/ATC]TTCTTTGCCTGCCTG | 9097 |
rs753203069 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:181934 | TGCCTATTATTTTGC[A/G]TGTGTATATCCAGTT | 9097 |
rs753208395 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:167125 | GTGGTGGTGCACGCC[C/T]GTAATCCTAGCTACT | 9097 |
rs753210334 | snp | C/T | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212449 | TCTCTACTAAAGATA[C/T]AAAAATTAGCTGGAT | 9097 |
rs753231790 | snp | A/G | 1.6566e-05 | 0.00287797 | intron-variant | USP14 | GRCh38.p7 | 18:192942 | TGATAGGAGTAAGAC[A/G]TTCTATTTTTCGCTC | 9097 |
rs753261960 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:173788 | GGTTATTTTTTTCAC[A/G]TGAGTATTTAGTGAG | 9097 |
rs753289375 | snp | A/G | 1.73483e-05 | 0.00294514 | intron-variant | USP14 | GRCh38.p7 | 18:209951 | TCATGATTTAAAATT[A/G]AACATTTTTTTCTCC | 9097 |
rs753314667 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:163923 | GTTCTCATTATTTAG[C/T]TCCCACTTACAAAAG | 9097 |
rs753328199 | snp | C/T | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212881 | TGTTGTTTTAATGCT[C/T]GGCAGAGCACAACAC | 9097 |
rs753329371 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:183748 | ATTTTTATTTAAAGG[-/T]TTTTTTTTTTTTTCC | 9097 |
rs753330679 | in-del | -/CTCC | 4.95503e-05 | 0.00497722 | intron-variant | USP14 | GRCh38.p7 | 18:204733 | TCTTAATATCTTAAT[-/CTCC]CTCCCATCAGTGCTC | 9097 |
rs753370525 | snp | A/G | 3.57226e-05 | 0.00422611 | intron-variant | USP14 | GRCh38.p7 | 18:211099 | AGACGAATCCTGCAT[A/G]ACATTAATTCATCTT | 9097 |
rs753397491 | snp | G/T | 1.64741e-05 | 0.00286998 | intron-variant | USP14 | GRCh38.p7 | 18:178918 | TTTTCATGAAATTAC[G/T]TTTTTTAAAAACAGG | 9097 |
rs753433764 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:190081 | AATGGGTCTGGCTCA[C/T]GATGTTTAGTGTATC | 9097 |
rs753573336 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:171913 | ACTTGAGTTGAGGAT[A/G]CAACTGCACATGTGG | 9097 |
rs753738544 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:184966 | ACTCCTGGAGTTAGA[G/T]TCTCAATTTAGAACC | 9097 |
rs753756245 | snp | C/T | 1.7704e-05 | 0.00297518 | synonymous-codon | USP14 | GRCh38.p7 | 18:199314 | TTTACAGGACTTAAA[C/T]TGGTAAGGACAATCT | 9097 |
rs753759576 | snp | C/T | 1.65312e-05 | 0.00287495 | intron-variant | USP14 | GRCh38.p7 | 18:202960 | TGTAAGTTATGCAGT[C/T]CTTTCGAAGCCAAAT | 9097 |
rs753822770 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:206300 | TGCACCTTCCTAGTG[A/G]CTGATGAAGTTGAGC | 9097 |
rs753853446 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:196838 | TTTACCGTACTTACT[A/G]GAACATAGTTCGAAA | 9097 |
rs754087613 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:192932 | TACTACTTTTTGATA[A/G]GAGTAAGACATTCTA | 9097 |
rs754132269 | in-del | -/TTT | | | intron-variant | USP14 | GRCh38.p7 | 18:173285 | GCTATTTTTTTTGTA[-/TTT]TTTTTAGTAGAGACG | 9097 |
rs754154529 | snp | A/G | 4.67213e-05 | 0.00483306 | intron-variant | USP14 | GRCh38.p7 | 18:163295 | ATTAAAAAAATTGTG[A/G]TTTTGTTTGCAGTTA | 9097 |
rs754166870 | snp | C/T | 1.65449e-05 | 0.00287614 | intron-variant | USP14 | GRCh38.p7 | 18:192930 | TATACTACTTTTTGA[C/T]AGGAGTAAGACATTC | 9097 |
rs754167084 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:160803 | CAGTATGCCTTCTTC[A/G]AGCCTGATTTCTCTG | 9097 |
rs754180233 | snp | A/G | 1.64833e-05 | 0.00287078 | synonymous-codon | USP14 | GRCh38.p7 | 18:163411 | GTTGACTGGAGTCCA[A/G]CCTGCCAGACAGAAA | 9097 |
rs754205086 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:156586 | GCAATGCACTGTGCT[A/G]AGAATCTTCTATACA | 9097 |
rs754246606 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:203857 | CCCGCTTTGGCCTCC[C/G]AAAGAGTTCCTTTCT | 9097 |
rs754396795 | in-del | -/C | | | intron-variant | USP14 | GRCh38.p7 | 18:205424 | TTTTCTTCTGCCCTA[-/C]CCCTTCCTTAATTCC | 9097 |
rs754498535 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:187613 | AGTAAGATGGATTTT[C/T]TTCACGTGTTTTATT | 9097 |
rs754548561 | in-del | -/TT | 6.60469e-05 | 0.00574622 | intron-variant | USP14 | GRCh38.p7 | 18:166766 | TGGTGGTTAAATGTC[-/TT]TTGTTTGTCTTTGAA | 9097 |
rs754593250 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:186501 | CTCATGCTTGTAATC[C/G]CAGCACTTTGGGAGG | 9097 |
rs754593609 | snp | A/G | 1.65211e-05 | 0.00287407 | intron-variant | USP14 | GRCh38.p7 | 18:196804 | TCATTCTGTAAATGT[A/G]AAACTTAGGTTTCCT | 9097 |
rs754619839 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:200596 | TCACATAAAATGTCA[C/G]CTTCCACTCTGCTAA | 9097 |
rs754632841 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:189830 | AGTATACAAATTATA[A/C]GTGTACAACTCAATG | 9097 |
rs754676603 | in-del | -/CATTCTATT | 6.62416e-05 | 0.00575469 | intron-variant | USP14 | GRCh38.p7 | 18:192940 | TTGATAGGAGTAAGA[-/CATTCTATT]CATTCTATTTTTCGC | 9097 |
rs754681408 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:195487 | GAAGAGTTTTGCTGT[A/G]CATGAAGGAGGGCAA | 9097 |
rs754760500 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:182666 | GGCTGCTATGAGAAC[A/G]TCTAAGGGAGTTCAT | 9097 |
rs754813807 | in-del | -/ATTA | | | intron-variant | USP14 | GRCh38.p7 | 18:189261 | CCTACTTTTGTTTGT[-/ATTA]ATTTTTTCTTATTTC | 9097 |
rs754814013 | snp | A/G | 6.88919e-05 | 0.00586866 | intron-variant | USP14 | GRCh38.p7 | 18:199151 | ATTATATTCAAGAGT[A/G]TATAACAAATTGAAT | 9097 |
rs755017859 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:190514 | ATTTAGAAACACATA[C/T]ATGAAAGCATATGTT | 9097 |
rs755037526 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:191594 | CCTTATCCTCTCCAC[C/T]CCCTTCCAGCAACTA | 9097 |
rs755078187 | in-del | -/TTGC | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214009 | ATAGATGATGATTGA[-/TTGC]TTGATGATTGATAGT | 9097 |
rs755153450 | in-del | -/ACAC | | | intron-variant | USP14 | GRCh38.p7 | 18:165370 | CCACTGGGCAGTAAA[-/ACAC]ACGTTGGAGGAAAAT | 9097 |
rs755234624 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:182380 | ATTTTTGTTTTTTCC[C/T]CTCAGTCTATTGTGA | 9097 |
rs755263440 | in-del | -/TG/TGTA | | | intron-variant | USP14 | GRCh38.p7 | 18:178028 | GTTTGTTTGTTTGTT[-/TG/TGTA]ATATTTTTTGAGACG | 9097 |
rs755277317 | in-del | -/CTTTT | 1.66059e-05 | 0.00288144 | frameshift-variant | USP14 | GRCh38.p7 | 18:210015 | AGTTAAGTATGAACC[-/CTTTT]CTTTTGCTGATGGTA | 9097 |
rs755287121 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:198682 | ATTATTTTTTCCTAA[G/T]AACATCTTTAGCAGA | 9097 |
rs755455699 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:165561 | GTACTTATTTTATGT[C/T]AGGCTTTTATTATAT | 9097 |
rs755468328 | snp | A/G | 1.79277e-05 | 0.00299392 | intron-variant | USP14 | GRCh38.p7 | 18:209940 | TATTTCCAAAATCAT[A/G]ATTTAAAATTAAACA | 9097 |
rs755545639 | in-del | -/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:197599 | ATTACTTACTTTGTC[-/T]TTTTTTTACATTACA | 9097 |
rs755713984 | snp | A/G | 1.67671e-05 | 0.00289539 | intron-variant | USP14 | GRCh38.p7 | 18:196593 | AGTCGCGTGTATTAA[A/G]TATGTGACTGTTTTA | 9097 |
rs755736359 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:189194 | GTATTTTAGTTTTCA[A/C]AGAATTGGCTATTAG | 9097 |
rs755740902 | in-del | -/TTTG | 0.000102142 | 0.00714568 | intron-variant | USP14 | GRCh38.p7 | 18:204545 | TGTTTACACATGTTT[-/TTTG]TTTGTTTGTATATAG | 9097 |
rs755786636 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:171606 | TTTGAGAGACATAAA[C/T]GAGATGAATGTTGTT | 9097 |
rs755951896 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:183731 | TTCTGAGGCTCTGAA[A/G]TATTTTTATTTAAAG | 9097 |
rs755954512 | snp | G/T | 1.70409e-05 | 0.00291893 | stop-gained | USP14 | GRCh38.p7 | 18:199295 | TCAGGAAGTCAAGTA[G/T]CTTTTTACAGGACTT | 9097 |
rs756067354 | snp | A/C/G | 1.65127e-05 | 0.00287334 | synonymous-codon | USP14 | GRCh38.p7 | 18:163447 | GGTGAAAGGAGGAAC[A/C/G]CTAAAGGTAAAATGT | 9097 |
rs756081649 | snp | C/T | 1.65373e-05 | 0.00287548 | intron-variant | USP14 | GRCh38.p7 | 18:198172 | ACTATACTCATACCT[C/T]ATTAGAATTGGCATA | 9097 |
rs756113709 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:195558 | AAATCCAAGAGAACA[C/G]ACTAGTCCATGACTG | 9097 |
rs756181569 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:179719 | CAGGCTCCTGAGTAG[C/T]GAAAATTGTAGGCGT | 9097 |
rs756216255 | snp | A/G | 1.6492e-05 | 0.00287154 | synonymous-codon | USP14 | GRCh38.p7 | 18:180298 | GAATGCCACAGTTCA[A/G]TGTATTCGTTCTGTG | 9097 |
rs756287358 | in-del | -/AGAT | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:213964 | TTTCTGTAATGGACA[-/AGAT]AGATAGATTAGATAG | 9097 |
rs756312690 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:159647 | TCTTGATGGTCTAGA[A/G]TCTTGAATCGAATTC | 9097 |
rs756321183 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:207446 | CACTTTGGGAGGCCA[A/C]GGTGGGCAGATTGCT | 9097 |
rs756386745 | in-del | -/TTTAT | | | intron-variant | USP14 | GRCh38.p7 | 18:200780 | TGATAATTAGGATTG[-/TTTAT]TTTATTTTATTTTAT | 9097 |
rs756443935 | snp | C/T | 8.96419e-05 | 0.00669424 | synonymous-codon | USP14 | GRCh38.p7 | 18:158713 | CATGCCGCTCTACTC[C/T]GGTGAGCCCTGTCCT | 9097 |
rs756449204 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:202161 | TCTTTCTGTGACATT[A/G]GAAATAGTAGTGAAT | 9097 |
rs756489561 | in-del | -/TT | | | intron-variant | USP14 | GRCh38.p7 | 18:160645 | AGCATGAGCAAAAAG[-/TT]TTTTAAGTAACTTGC | 9097 |
rs756490319 | in-del | -/TC | | | intron-variant | USP14 | GRCh38.p7 | 18:162602 | AAACTATCTAACCTT[-/TC]TCTCTCTCTCTTCTT | 9097 |
rs756500857 | snp | A/C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:168216 | CAGGCGTGAGCCACC[A/C/G]CACCCGGCCAAAATA | 9097 |
rs756553879 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:181937 | CTATTATTTTGCATG[C/T]GTATATCCAGTTCTT | 9097 |
rs756613574 | in-del | -/AAAAATATATAT | | | intron-variant | USP14 | GRCh38.p7 | 18:171021 | CTTAAAAAAAAAAAA[-/AAAAATATATAT]AAAAATATATATATA | 9097 |
rs756624822 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:167151 | CTACTCGGGAGGCTG[A/G]GGTGGGAGGCTGAGG | 9097 |
rs756624943 | snp | C/T | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212558 | GCAGTGAGCTGAGAT[C/T]ACACCACTGCACTCC | 9097 |
rs756633864 | in-del | -/AGTT | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214106 | GCTGGAGCCATAGAC[-/AGTT]AGTTAGTTAGTTAGT | 9097 |
rs756674985 | snp | C/T | 5.61656e-05 | 0.00529902 | intron-variant | USP14 | GRCh38.p7 | 18:163290 | TTTTAATTAAAAAAA[C/T]TGTGATTTTGTTTGC | 9097 |
rs756796146 | snp | A/G | 1.73884e-05 | 0.00294854 | missense | USP14 | GRCh38.p7 | 18:163337 | GGAAAGGAGAAATTT[A/G]AAGGTGTAGAATTGA | 9097 |
rs756798014 | snp | C/T | 1.65258e-05 | 0.00287448 | intron-variant | USP14 | GRCh38.p7 | 18:198159 | AGCCAAGATATAGAC[C/T]ATACTCATACCTTAT | 9097 |
rs756827725 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:164064 | GCATCATTTAAATTT[G/T]ATTTTAAAATGTGTT | 9097 |
rs756907915 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:175389 | TGGCTGGTGGTAGTT[G/T]ATAGATGTTCATCAT | 9097 |
rs756992769 | snp | A/G | 1.65828e-05 | 0.00287943 | missense | USP14 | GRCh38.p7 | 18:211159 | AAGTTTGATGATGAC[A/G]AAGTCAGCATCGTAA | 9097 |
rs757027356 | snp | A/G | 1.64953e-05 | 0.00287182 | synonymous-codon | USP14 | GRCh38.p7 | 18:163438 | GAAAGTTATGGTGAA[A/G]GGAGGAACGCTAAAG | 9097 |
rs757043354 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:199844 | AAGGCTGGCGGGAAT[C/T]TAATCCTGTATTTCC | 9097 |
rs757171789 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:186209 | GCTCATGCCTGTGAT[A/C]CCAGTGCTTTGGGAG | 9097 |
rs757210559 | snp | A/G | 3.30349e-05 | 0.00406403 | synonymous-codon | USP14 | GRCh38.p7 | 18:198073 | ATCTGCATCGGCAGC[A/G]ACACCTTCTAAAAAG | 9097 |
rs757259168 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:177656 | TTTTTTTTAAATCTC[C/T]ACTTCTGGTCCTACC | 9097 |
rs757290842 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:168287 | TAAGCAATTCACTTA[C/G]TAATTCCAGTTGTGT | 9097 |
rs757318075 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:188068 | TTAAATAGTAGATGG[-/T]TGTGGAATTCTCTCT | 9097 |
rs757347922 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:181249 | TTTCATATAGTAACT[C/T]TATGTTTAATGTTTT | 9097 |
rs757355988 | snp | C/G | 3.31395e-05 | 0.00407046 | intron-variant | USP14 | GRCh38.p7 | 18:202985 | CCAAATTCCGCTTCA[C/G]TGAAATATTTCCAGT | 9097 |
rs757380343 | snp | A/G | 1.64936e-05 | 0.00287168 | missense | USP14 | GRCh38.p7 | 18:180281 | GGTAACACTTGTTAC[A/G]TGAATGCCACAGTTC | 9097 |
rs757436631 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:194131 | TAGCCATCCAAGAGG[A/T]ATGAAGTGTTATCTC | 9097 |
rs757599669 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:156609 | TCTATACATAATCTT[A/T]TTTAGTCCTTATAAC | 9097 |
rs757614604 | snp | A/G | 1.64792e-05 | 0.00287042 | missense | USP14 | GRCh38.p7 | 18:196757 | GTGAACAAGGACAGT[A/G]TCTTCAACAGGTAAT | 9097 |
rs757668904 | in-del | -/AG | | | intron-variant | USP14 | GRCh38.p7 | 18:159801 | ATGCCAGCGCTGACC[-/AG]AGTTTCTTTTTTAAA | 9097 |
rs757711564 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:204054 | TGAGCTTAAATTCTT[A/G]GTATATTTTCCAGTA | 9097 |
rs757724066 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:169256 | ATTAGCCGAGTGTCA[C/T]GGTGCACGCCAAGAG | 9097 |
rs757743005 | snp | C/T | 0.000105048 | 0.00724657 | utr-variant-5-prime | USP14 | GRCh38.p7 | 18:158672 | GGCCCAGCTCTCCTG[C/T]GCCGCCGCCTCCCGC | 9097 |
rs757757173 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:188772 | AACCTCCGCCTCCTG[A/G]GTTCGAGCGATTCTC | 9097 |
rs757769079 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:163774 | CAGGGTTTCAATGTA[C/T]GGATTTCATCACCCA | 9097 |
rs757805750 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:186297 | CCCGCATCTCTGCAA[C/T]AAAAAAGAAATAGCT | 9097 |
rs757838180 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:202259 | AACAATAACACTATA[A/C]CATTGATTACCACTA | 9097 |
rs757861261 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:198354 | ACAGTTCTGCCTCAG[C/T]CTCCCAAGTAGCTGG | 9097 |
rs757981348 | snp | A/G | 4.95291e-05 | 0.00497615 | missense | USP14 | GRCh38.p7 | 18:211247 | TACTCTATGGGCCTC[A/G]CAGAGTTGAAATAAT | 9097 |
rs757997899 | snp | C/G | 0.000100771 | 0.00709756 | intron-variant | USP14 | GRCh38.p7 | 18:158722 | CTACTCCGGTGAGCC[C/G]TGTCCTGGCCTCGCG | 9097 |
rs758025012 | snp | C/T | 3.45955e-05 | 0.00415891 | intron-variant | USP14 | GRCh38.p7 | 18:163302 | AAATTGTGATTTTGT[C/T]TGCAGTTACTGTAAA | 9097 |
rs758067980 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:196955 | CTTTGCCCCTTTGCA[C/G]TTTCTCTACACAGCC | 9097 |
rs758083695 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:209411 | TTTTCTCATGTTGCA[C/T]GCTAAAATGAGTTGA | 9097 |
rs758088629 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:165399 | AAAATCTTTGTTTAC[C/T]CCCGAAGGTACAGTA | 9097 |
rs758099371 | snp | A/G | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213279 | GACCAGGTGAGCTAG[A/G]TTTAGAGCAAAGTAT | 9097 |
rs758112641 | in-del | -/GAA | 0.0464853 | 0.145196 | cds-indel | USP14 | GRCh38.p7 | 18:199221 | AAATGTACAGAATCT[-/GAA]GAAGAAGAAGTCACC | 9097 |
rs758137848 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:192953 | AGACATTCTATTTTT[C/T]GCTCACAATCCTTTG | 9097 |
rs758154648 | snp | C/T | 1.67052e-05 | 0.00289004 | intron-variant, missense | USP14 | GRCh38.p7 | 18:178969 | GGGTCAGCAGATGCT[C/T]TTCCAGAAGAACCCT | 9097 |
rs758160314 | in-del | -/A | | | intron-variant | USP14 | GRCh38.p7 | 18:163282 | TGTTATTTTTTAATT[-/A]AAAAAAATTGTGATT | 9097 |
rs758219441 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:207778 | TTTTATAGTTTTCAG[C/T]GTACAAGCCTTGGAC | 9097 |
rs758333725 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:187364 | TAATGCATACTTCTT[A/T]CTTTCAGTGTATTAC | 9097 |
rs758386531 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:173019 | TTGTAAGAAATCTTC[A/G]CCTGTGCCAAGTTTA | 9097 |
rs758410341 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:156683 | ATTGCTAGTTTAGTT[C/G]CAGACCACTGCAATA | 9097 |
rs758418829 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157779 | TCACTGGAACAGATA[C/T]AATAGTATTTAAAAA | 9097 |
rs758458217 | in-del | -/AC | | | intron-variant | USP14 | GRCh38.p7 | 18:179464 | ATGTGGAAAATACAT[-/AC]ATTTTATCCTGAATT | 9097 |
rs758505078 | snp | A/C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:204192 | TAAAGTTGTATTTCA[A/C/T]ATAAAAAAAAAAAAC | 9097 |
rs758508361 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:159756 | CAGTAGATTCACACA[C/T]ATAAAACAAAACCCC | 9097 |
rs758534846 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:169496 | GTGATTTTTTTTTCT[C/T]TTTTTCTGTTGGTAG | 9097 |
rs758563474 | snp | A/G | 1.6563e-05 | 0.00287771 | intron-variant | USP14 | GRCh38.p7 | 18:166840 | TATTATCTTATGAAC[A/G]TTTATTATAATGCAG | 9097 |
rs758573068 | snp | C/T | 4.96619e-05 | 0.00498282 | intron-variant | USP14 | GRCh38.p7 | 18:202978 | TTCGAAGCCAAATTC[C/T]GCTTCACTGAAATAT | 9097 |
rs758595138 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:168366 | CAAATAATGACAATT[A/T]TACTTCTCCCTTTTC | 9097 |
rs758621248 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:164131 | ACACTTTACAGTTAT[C/G]TGTATTGTGTGAATT | 9097 |
rs758628021 | snp | C/T | 2.11723e-05 | 0.00325357 | intron-variant | USP14 | GRCh38.p7 | 18:199365 | TGAATTCCATGTTTG[C/T]GAGTAAGCCAAAGTC | 9097 |
rs758760898 | snp | C/T | 1.71675e-05 | 0.00292976 | intron-variant | USP14 | GRCh38.p7 | 18:209956 | ATTTAAAATTAAACA[C/T]TTTTTTCTCCTCAGA | 9097 |
rs758840278 | snp | G/T | 0.000166016 | 0.00910937 | intron-variant | USP14 | GRCh38.p7 | 18:192948 | GAGTAAGACATTCTA[G/T]TTTTCGCTCACAATC | 9097 |
rs758849710 | snp | A/G | 1.65048e-05 | 0.00287265 | synonymous-codon | USP14 | GRCh38.p7 | 18:204671 | TCTAGAAGATAAAAA[A/G]GTGAATCAGCAGCCA | 9097 |
rs758863024 | in-del | -/TG | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213237 | TTTAGATTTTCTGAC[-/TG]TAGCTACTAAATGTT | 9097 |
rs758890733 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:191338 | AAAAACAAAATCCTT[C/T]AATTGAGTACAATTT | 9097 |
rs758930588 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157599 | TAATTCTAGTTCTCT[C/T]GCTATTGCCACCACA | 9097 |
rs758940536 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:190203 | CTGTTGATGAATATT[C/T]GGTTTATGTTCAGTT | 9097 |
rs758971275 | in-del | -/AA | | | intron-variant | USP14 | GRCh38.p7 | 18:169362 | CAAGACTCTACCTCA[-/AA]AAAAAAAAAAAAAAA | 9097 |
rs758985407 | in-del | -/T | 1.64773e-05 | 0.00287026 | intron-variant | USP14 | GRCh38.p7 | 18:209956 | ATTTAAAATTAAACA[-/T]TTTTTTCTCCTCAGA | 9097 |
rs759004066 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:203432 | ATCTGGGTAGGTCTT[C/T]GGTGGGGCCTAGGAT | 9097 |
rs759008229 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:188881 | ACGTGGTTTCACCAT[A/G]TTGGCCAGGATGGTC | 9097 |
rs759044464 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:182299 | TGTCTTGATACATAA[A/G]TTGTCAGTTCTTTAT | 9097 |
rs759059391 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:201935 | GAGTAATTTGGCTTC[A/G]TTTCTCCACTGCTTT | 9097 |
rs759059929 | snp | A/G | 2.04627e-05 | 0.00319858 | intron-variant | USP14 | GRCh38.p7 | 18:180191 | ATGTCATTTTGTAAA[A/G]ATGGTTTAATGATTT | 9097 |
rs759085766 | in-del | -/AT | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213127 | ATGATTCATGTATAT[-/AT]TTGTATGATGCTTGT | 9097 |
rs759174879 | snp | C/T | 1.65551e-05 | 0.00287702 | intron-variant | USP14 | GRCh38.p7 | 18:180356 | TAAGACTGCAGTCTT[C/T]TTTGGGTAAGGGATG | 9097 |
rs759195662 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:163514 | TTTTTGAAAAATAAC[A/G]CCAGAAAATTATTTA | 9097 |
rs759203745 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:203214 | TGAACTTTACTTTGT[A/G]TAAGAAATGTAATTC | 9097 |
rs759243363 | in-del | -/TTTAT | | | intron-variant | USP14 | GRCh38.p7 | 18:200786 | ATTAGGATTGTTTAT[-/TTTAT]TTTATTTTATTTATT | 9097 |
rs759249599 | in-del | -/TTG | 0.000340703 | 0.0130474 | intron-variant | USP14 | GRCh38.p7 | 18:199340 | AATCTCAGTCCATCC[-/TTG]TTGTTTGTGAATTCC | 9097 |
rs759279738 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:156908 | ACATGGCGAAATCCC[A/G]TCTTTACAAAACATA | 9097 |
rs759354206 | snp | C/G | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212278 | CAGTCAGATTCTTTC[C/G]TTGGCTCAGTTGTGT | 9097 |
rs759405889 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:183800 | CTGTTCTTTTTGGAT[A/G]TAAGGGTTGTTCTTC | 9097 |
rs759433234 | snp | A/C/T | 4.94999e-05 | 0.00497473 | intron-variant | USP14 | GRCh38.p7 | 18:203082 | AATGGGATTTCTTTA[A/C/T]ATTTTGTCTCCTCAG | 9097 |
rs759449793 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:189902 | GCAGAACCCTTCTAG[C/T]ACTCTAAAAATCCCC | 9097 |
rs759478554 | snp | C/T | 0.000248026 | 0.0111334 | intron-variant | USP14 | GRCh38.p7 | 18:202965 | GTTATGCAGTCCTTT[C/T]GAAGCCAAATTCCGC | 9097 |
rs759484005 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:207073 | TTTTAAGAAGACTGT[C/T]CTTTGCCCATCAGAT | 9097 |
rs759506408 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:210062 | ATTTTAATTGAGTTA[C/T]TGTATGTGGGTCTTT | 9097 |
rs759730508 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:172703 | AACTGAAGGCTTAGA[C/T]GATTGTCAGCTTTTT | 9097 |
rs759753648 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:187098 | TAAATATTTTTTGAC[C/T]ACTGGTAAGATTGAA | 9097 |
rs759757238 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:194666 | CTGGGTGCGGTGGCT[C/T]ATGCTTGTAATCCCA | 9097 |
rs759785636 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:185777 | ACAGATCACTGCAGC[C/G]TTGACCTCTTGGGCT | 9097 |
rs759794263 | snp | C/T | 1.64833e-05 | 0.00287078 | stop-gained | USP14 | GRCh38.p7 | 18:163421 | GTCCAGCCTGCCAGA[C/T]AGAAAGTTATGGTGA | 9097 |
rs759814933 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:199587 | GGTTATTTCACTGTT[G/T]AAGATGACCCCCCAA | 9097 |
rs759879945 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:187792 | AATATTGAAATAGTC[C/T]TTATATTCTATGAAA | 9097 |
rs759892412 | snp | A/C | 3.295e-05 | 0.00405881 | synonymous-codon | USP14 | GRCh38.p7 | 18:196698 | TCCACCTATTATTCT[A/C]CTGCAGTTTTTGCAC | 9097 |
rs759931754 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:192559 | GACAAGAGCAAAACT[C/G]TGTCTCAGAAAATAA | 9097 |
rs759959680 | snp | A/C | 1.67377e-05 | 0.00289284 | missense | USP14 | GRCh38.p7 | 18:199232 | ATCTGAAGAAGAAGA[A/C]GTCACCAAAGGAAAG | 9097 |
rs759994025 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:161589 | CCCCCCCATTAGGCT[A/G]TAAGTTTATGGAGAG | 9097 |
rs760006407 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:193573 | TCCAAAAAGCAACTT[C/T]ATAACATCTAGCAGT | 9097 |
rs760055141 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:208966 | GGCCAGGCTGGTCTC[A/G]AGCTCCTGATCTCAA | 9097 |
rs760065122 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:160355 | ATTAAATGGTTAAGG[A/G]TAAGTGCAGTTAAAA | 9097 |
rs760072237 | in-del | -/A | | | intron-variant | USP14 | GRCh38.p7 | 18:193156 | TCAGGTTTGATTTGT[-/A]TAATACATATCTTTG | 9097 |
rs760114147 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:175145 | ATTTTTATAATTGAC[C/T]TTGTATCCTGTGACT | 9097 |
rs760164765 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:190016 | CCAGTTTTGAACTCT[A/G]TGAACAGAAATGTAC | 9097 |
rs760198552 | snp | A/G | 3.30278e-05 | 0.0040636 | missense | USP14 | GRCh38.p7 | 18:202913 | ACCAAACAGTCTCCA[A/G]CGTTGCAAAGAAATG | 9097 |
rs760299516 | snp | A/G | 3.30792e-05 | 0.00406675 | intron-variant | USP14 | GRCh38.p7 | 18:203072 | ATTTTGATGTAATGG[A/G]ATTTCTTTACATTTT | 9097 |
rs760449397 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:166243 | ATTTGATGCTGTAAA[C/T]ACAGGTTACTGCCTT | 9097 |
rs760498535 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:178516 | TGTACAGTTTGATGA[C/T]TTTGGGCGATTCTAT | 9097 |
rs760556861 | snp | A/G | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214178 | CAAGACTCGTGGCAG[A/G]CAGAACAAACCATCA | 9097 |
rs760643555 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:184359 | AAACAAGAATGAAAG[A/G]ACAGAAAAACATTCC | 9097 |
rs760681329 | snp | G/T | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212819 | CTGATTTTGAGTTAT[G/T]TATAATAAAGTTTGG | 9097 |
rs760764076 | snp | A/G | 1.65255e-05 | 0.00287445 | intron-variant | USP14 | GRCh38.p7 | 18:166740 | TATTAGATTGTGTTC[A/G]GCTTGTACAGTGGTG | 9097 |
rs760847606 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:160659 | AGTTTTAAGTAACTT[C/G]CTCATGGCAATAGCA | 9097 |
rs760877343 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:173564 | TTAAAGGCATGCACC[A/G]CCACACCCAGCTAAT | 9097 |
rs760942800 | snp | A/G | 1.65291e-05 | 0.00287476 | intron-variant | USP14 | GRCh38.p7 | 18:192921 | TATACTAAATATACT[A/G]CTTTTTGATAGGAGT | 9097 |
rs760987386 | in-del | -/T/TT | 0.17086 | 0.24598 | intron-variant | USP14 | GRCh38.p7 | 18:180211 | TTAATGATTTAATCC[-/T/TT]TTTTTTTTTTTTTTT | 9097 |
rs760988543 | snp | A/T | 3.30431e-05 | 0.00406454 | intron-variant | USP14 | GRCh38.p7 | 18:204742 | TCTTAATCTCCCATC[A/T]GTGCTCAGCAATTAC | 9097 |
rs761144470 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:194824 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCACG | 9097 |
rs761193613 | in-del | -/C | | | intron-variant | USP14 | GRCh38.p7 | 18:177966 | TGTAAACAATCACTA[-/C]AGTTACACAATAGAC | 9097 |
rs761268220 | in-del | -/G | | | intron-variant | USP14 | GRCh38.p7 | 18:184863 | TGGATTAGCTTAAGA[-/G]GCAGTAAGGATCAAG | 9097 |
rs761300500 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:176780 | TTTTACATTTAAATC[-/T]TTTAATTAATTGTTG | 9097 |
rs761326823 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:178841 | AAATAGAATTATGTT[A/G]TATGTGTTCTTTTGT | 9097 |
rs761347782 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:191224 | TTAAAAATGAACACA[A/C]ATAATTCAGGCATTA | 9097 |
rs761451467 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:192064 | TCATTTAATAGAAGC[G/T]TCTCAGTTTACAGAT | 9097 |
rs761515952 | snp | C/T | 1.66554e-05 | 0.00288573 | intron-variant | USP14 | GRCh38.p7 | 18:202867 | TTTGGTCTTCTGTTA[C/T]GTTCTTTCTTAGCGA | 9097 |
rs761536377 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:206339 | ATGTGTTTATTTGCT[A/G]TCTGTATATCCTCTT | 9097 |
rs761570946 | snp | A/G | 1.67307e-05 | 0.00289224 | missense | USP14 | GRCh38.p7 | 18:199266 | AATCAACTTCAGCTT[A/G]GCTGTTTTATCAATC | 9097 |
rs761572728 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:199852 | CGGGAATCTAATCCT[G/T]TATTTCCCCTAGGAG | 9097 |
rs761630323 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:187258 | AAATATTTTTGAGAC[C/T]TGTTCCTAGATTTTC | 9097 |
rs761742652 | in-del | -/AG | | | intron-variant | USP14 | GRCh38.p7 | 18:210143 | TTCAAACAAAATGTC[-/AG]GTTTCTTGAACAATT | 9097 |
rs761767613 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:166445 | TCAAGCAATTATCTT[A/G]TCTCAGCCTCCCGAG | 9097 |
rs761777095 | snp | A/T | 6.56879e-05 | 0.00573059 | intron-variant | USP14 | GRCh38.p7 | 18:163283 | TGTTATTTTTTAATT[A/T]AAAAAATTGTGATTT | 9097 |
rs761782488 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:198259 | TTTTTTTCTTTGAGA[C/T]GGAGTTTCGCTCTTG | 9097 |
rs761795940 | in-del | -/C | | | intron-variant | USP14 | GRCh38.p7 | 18:188526 | TTTTTTTTTTTTTTT[-/C]CTTTGTGAGGGTTTG | 9097 |
rs761796010 | in-del | -/CAT | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212846 | TGGGGATTATCATAA[-/CAT]CATCTCATATCTTTG | 9097 |
rs761855721 | snp | G/T | 1.64985e-05 | 0.0028721 | missense | USP14 | GRCh38.p7 | 18:198114 | TCGATCAGTTCTTCG[G/T]TGTTGAGTTTGAAAC | 9097 |
rs761858604 | snp | A/G | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212140 | AAGATGGTTATTAAC[A/G]CTGTGCTGTTAAGCA | 9097 |
rs761937317 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:195052 | TTTTTTTTTTCCTTC[C/T]TCAGGATTCAGTTTA | 9097 |
rs762045934 | snp | A/C | 1.66751e-05 | 0.00288744 | missense | USP14 | GRCh38.p7 | 18:204609 | TATGAACTGTGTACA[A/C]CAGAACTTCAAGAGA | 9097 |
rs762066490 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:210585 | TTTCAAACTTTGGGT[A/C]TCAGAACCACTTTAC | 9097 |
rs762160698 | snp | C/T | 1.79774e-05 | 0.00299806 | intron-variant | USP14 | GRCh38.p7 | 18:211094 | CTCTGAGACGAATCC[C/T]GCATAACATTAATTC | 9097 |
rs762221512 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157413 | AGTTCCATAGTTTAT[C/G]ATATTCTAAATCCTT | 9097 |
rs762229330 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:205450 | ATTCCTGACAACTAC[C/G]AACCCGTTCATTTCT | 9097 |
rs762266167 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:167911 | TCATGGCTAGAATGT[A/G]AAAATACAATTGATT | 9097 |
rs762269209 | snp | C/T | 2.92094e-05 | 0.0038215 | intron-variant | USP14 | GRCh38.p7 | 18:197998 | TGTGTGGAAGAAAAT[C/T]TACATTAATATTTAT | 9097 |
rs762276604 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:170766 | ACAGGAACAGAAAAC[C/T]GAACACCGCATGTTG | 9097 |
rs762330154 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:184481 | TATGGGTCCCGAGTG[C/T]GATGGCTCACGCCTG | 9097 |
rs762441039 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:166552 | TGGTCCGGCTGGTTT[C/T]GAACTCCTGACCGCA | 9097 |
rs762471553 | snp | G/T | 1.64798e-05 | 0.00287047 | synonymous-codon | USP14 | GRCh38.p7 | 18:192851 | TCCTAGGTATGCAGG[G/T]GCCTTGAGAGCTTCA | 9097 |
rs762475897 | snp | A/G | 1.65211e-05 | 0.00287407 | intron-variant | USP14 | GRCh38.p7 | 18:198151 | TCCTTATGAGCCAAG[A/G]TATAGACTATACTCA | 9097 |
rs762589952 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:173635 | TCCATGTTGGTCAGG[A/C]TGGTCTTGAACTCCT | 9097 |
rs762598099 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:205124 | CAGGCGATCTGCCCA[C/G]CTAGGCCTCCCAGAG | 9097 |
rs762619081 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:181310 | ACGGTACCATTTTAC[A/G]TTCTCACCAGCAATG | 9097 |
rs762722721 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:188719 | GTCTCGCTGTGTTGC[C/G]CAGGCTGGAGTGCAG | 9097 |
rs762742728 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:189780 | CCACCATGCCTGGCG[C/T]GTTTATTTTTGATTA | 9097 |
rs762779633 | snp | C/T | 1.64982e-05 | 0.00287208 | missense | USP14 | GRCh38.p7 | 18:203110 | CAGTCCAAGATCAGC[C/T]GGCTGCCTGCTTACT | 9097 |
rs762809687 | snp | C/T | 1.66114e-05 | 0.00288192 | intron-variant | USP14 | GRCh38.p7 | 18:180373 | TTGGGTAAGGGATGT[C/T]CACATTTGGATGAGT | 9097 |
rs762828141 | in-del | -/GTATT | 1.67407e-05 | 0.00289311 | intron-variant | USP14 | GRCh38.p7 | 18:180390 | ACATTTGGATGAGTA[-/GTATT]GTTTTGTTTTGCTTT | 9097 |
rs762846082 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:167301 | AAAGAGTCTTGAAAT[A/G]AGATAGTATATGTTC | 9097 |
rs762856389 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:201891 | TTTATAACTTTTAAG[A/G]TATTTTATCTTTTGT | 9097 |
rs762858132 | snp | A/T | 1.69043e-05 | 0.00290721 | missense | USP14 | GRCh38.p7 | 18:204595 | TTATGTTGGATATGT[A/T]TGAACTGTGTACACC | 9097 |
rs762876363 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:185541 | AGAACTGAGACACTC[A/G]GAGAGAACAGAAAAG | 9097 |
rs762883633 | in-del | -/TACCATGATAGATTCTT | 1.70243e-05 | 0.00291751 | frameshift-variant | USP14 | GRCh38.p7 | 18:199212 | AAAGCATGAAATGTA[-/TACCATGATAGATTCTT]CAGAATCTGAAGAAG | 9097 |
rs762961936 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:209209 | TGTTTCTTTGTATAG[-/T]TTTTTTCAGTGATTG | 9097 |
rs763033194 | in-del | -/TGTT | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213645 | GGTTAGGCCTAAGAG[-/TGTT]TGTTTACCGAATAAT | 9097 |
rs763153433 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:184525 | TTGGGAGGCCGAGGC[A/G]GGTATCTCACTTGAG | 9097 |
rs763196556 | in-del | -/TG | | | intron-variant | USP14 | GRCh38.p7 | 18:186744 | GTGACAGAGGGAGAC[-/TG]TGTCTCAAAAAAAAA | 9097 |
rs763290145 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:160278 | CATTGCACTTCAGTC[G/T]GGGTGAAAAAAGCGA | 9097 |
rs763291839 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:198526 | GCCCAGCCCAGAGGT[A/T]TTTATACCTAAAAAA | 9097 |
rs763370563 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:192436 | GGGCATGATGGTGGA[C/T]GCCTGTAATCCCAGC | 9097 |
rs763411345 | snp | A/C | 1.80984e-05 | 0.00300813 | intron-variant | USP14 | GRCh38.p7 | 18:211084 | TGCAGTGGAACTCTG[A/C]GACGAATCCTGCATA | 9097 |
rs763466662 | snp | C/T | 6.75847e-05 | 0.00581273 | intron-variant | USP14 | GRCh38.p7 | 18:210337 | CTTAGCTTGAGAAGG[C/T]ACATGTCTATTCATT | 9097 |
rs763473127 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:172626 | CCTTCAGGAACCAGT[C/G]CCGTGATCAGTCAGT | 9097 |
rs763572998 | in-del | -/AC | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157396 | GCTGCTGTTTTATCA[-/AC]AGTTCCATAGTTTAT | 9097 |
rs763621717 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:175202 | TATTGTTAGGTATAC[A/G]TGTCATCTGCAAATA | 9097 |
rs763726140 | in-del | -/T | 8.25675e-05 | 0.00642471 | intron-variant | USP14 | GRCh38.p7 | 18:204727 | TTTATACTCTTAATA[-/T]CTTAATCTCCCATCA | 9097 |
rs763757165 | snp | A/G | 0.000314089 | 0.0125278 | missense | USP14 | GRCh38.p7 | 18:211255 | GGGCCTCGCAGAGTT[A/G]AAATAATGGAAGAGG | 9097 |
rs763804226 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157289 | TCATGAAAGTTTTCC[C/T]TGTGACATGCAGTGC | 9097 |
rs763840357 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:161847 | CTATTTTATGAGGCT[G/T]ATTGAAATTTTTTAT | 9097 |
rs763864058 | snp | C/T | 1.65496e-05 | 0.00287655 | synonymous-codon | USP14 | GRCh38.p7 | 18:203178 | GGAATCTGTGAATGC[C/T]AAAGTTCTTAAGGTT | 9097 |
rs763877524 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:203766 | AGGCGCCCGCCACCG[C/T]GCCCGGCTAATTTTT | 9097 |
rs763986439 | in-del | -/TCTG | | | intron-variant | USP14 | GRCh38.p7 | 18:204758 | GTGCTCAGCAATTAC[-/TCTG]TCTTTTTTTTCCTGC | 9097 |
rs763991170 | snp | A/G | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212848 | GGGGATTATCATAAC[A/G]TCTCATATCTTTGTG | 9097 |
rs764048870 | snp | A/T | 0.000116468 | 0.00763022 | intron-variant | USP14 | GRCh38.p7 | 18:180379 | AAGGGATGTTCACAT[A/T]TGGATGAGTAGTATT | 9097 |
rs764063202 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:176390 | GCACCTAGGCTCAAG[C/T]AGTACTCCCACCTTA | 9097 |
rs764087260 | in-del | -/TA | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157912 | CACAAACCTTCAATT[-/TA]TATATATATATATAT | 9097 |
rs764177201 | snp | C/G | 1.80494e-05 | 0.00300406 | utr-variant-5-prime, downstream-variant-500B | USP14, LOC105371951 | GRCh38.p7 | 18:158653 | CCCTTTGCCGCCCTC[C/G]TCAGGCCCAGCTCTC | 9097 |
rs764178040 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:194059 | CCCAGAAGGGTATGA[A/G]GGTTCTGATTTCTCT | 9097 |
rs764239134 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:209357 | TTCATTACCATTATA[A/G]TTTTAAAGAACTTTG | 9097 |
rs764255467 | snp | A/T | 7.26032e-05 | 0.00602464 | intron-variant | USP14 | GRCh38.p7 | 18:163274 | ATCTTGTCTTGTTAT[A/T]TTTTAATTAAAAAAA | 9097 |
rs764280565 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:161968 | ACTGTCACCTTCATT[C/T]ACATCCTCTTGCAAA | 9097 |
rs764301715 | snp | C/T | 1.65356e-05 | 0.00287533 | synonymous-codon | USP14 | GRCh38.p7 | 18:197621 | TACATTACAGGATGC[C/T]AATGAATGTTGGATA | 9097 |
rs764340864 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:202181 | TAGTAGTGAATGTTT[A/G]TTAAATGTAGAGTAT | 9097 |
rs764369912 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:169248 | ATACAAAAATTAGCC[A/G]AGTGTCATGGTGCAC | 9097 |
rs764376343 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:210355 | ATGTCTATTCATTGT[C/T]TAATATTAATGGATT | 9097 |
rs764414638 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:189987 | CTGACTTCTAATCTC[A/G]TAGATCAATTTTACC | 9097 |
rs764421810 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:167570 | GAGCACAGTGGCATG[A/G]TCATGGCTCGCTGCA | 9097 |
rs764438550 | in-del | -/G | | | intron-variant | USP14 | GRCh38.p7 | 18:195972 | GTTAAGATTTAAAAA[-/G]GATTTTTTTTTTTCT | 9097 |
rs764492193 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:183378 | TGTGGGTTTTATTTA[C/T]CTTATAAAAGTACTC | 9097 |
rs764530928 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon | USP14 | GRCh38.p7 | 18:196740 | ACAGTTTGCCGAGAA[A/G]GGTGAACAAGGACAG | 9097 |
rs764577935 | in-del | -/GAT | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:213998 | ATAGATAGATAGATA[-/GAT]GATGATTGATTGATG | 9097 |
rs764595490 | snp | A/G | 2.51196e-05 | 0.00354389 | intron-variant | USP14 | GRCh38.p7 | 18:178891 | GACATAAACATTACC[A/G]ACTTTTAAGGATTTT | 9097 |
rs764600687 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:166538 | GAGTTTCTTTATATT[G/T]GTCCGGCTGGTTTCG | 9097 |
rs764608623 | snp | A/G | 1.75372e-05 | 0.00296113 | intron-variant | USP14 | GRCh38.p7 | 18:211110 | GCATAACATTAATTC[A/G]TCTTCTTGTCCCTGT | 9097 |
rs764609140 | snp | C/T | 0.000108992 | 0.00738133 | intron-variant | USP14 | GRCh38.p7 | 18:211087 | AGTGGAACTCTGAGA[C/T]GAATCCTGCATAACA | 9097 |
rs764623469 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:194839 | GGGAGGCTGAGGCAC[A/G]AGAATCGCTTGAACC | 9097 |
rs764656091 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:179049 | TGCTGTAAGACACAC[C/T]AGATTTTATGTGTTT | 9097 |
rs764737133 | in-del | -/T | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:156733 | ATGAGTCACACAAAG[-/T]TTTTGTTTTCCCAGT | 9097 |
rs764764379 | snp | A/G | 1.93358e-05 | 0.00310927 | intron-variant | USP14 | GRCh38.p7 | 18:180207 | ATGGTTTAATGATTT[A/G]ATCCTTTTTTTTTTT | 9097 |
rs764917497 | snp | A/G | 1.65029e-05 | 0.00287248 | synonymous-codon | USP14 | GRCh38.p7 | 18:211242 | CGTTCTACTCTATGG[A/G]CCTCGCAGAGTTGAA | 9097 |
rs764929624 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:176614 | ATGGTATAGTTTTGC[C/T]CCTAGTTTATTGTTT | 9097 |
rs764943358 | in-del | -/G | | | intron-variant | USP14 | GRCh38.p7 | 18:198968 | AGCTTATAGTTTAGA[-/G]TTTATTGCAGTTTAT | 9097 |
rs764950466 | snp | A/G | 3.30737e-05 | 0.00406642 | intron-variant | USP14 | GRCh38.p7 | 18:202966 | TTATGCAGTCCTTTC[A/G]AAGCCAAATTCCGCT | 9097 |
rs764998147 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:176659 | GACATTTTTAAGATT[G/T]GTGTAGCTAGTTACA | 9097 |
rs765020777 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:191287 | AATTCGTTGAGTCAC[A/G]TCAGTTTCCGAAAGA | 9097 |
rs765153579 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:187260 | ATATTTTTGAGACCT[A/G]TTCCTAGATTTTCTA | 9097 |
rs765156848 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:198267 | TTTGAGACGGAGTTT[C/T]GCTCTTGTCGCCCAG | 9097 |
rs765165484 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:200038 | TAACAAATATTGGGA[A/C]ATCTCACTTTTTAAT | 9097 |
rs765238946 | snp | A/T | 1.76052e-05 | 0.00296686 | intron-variant | USP14 | GRCh38.p7 | 18:178924 | TGAAATTACTTTTTT[A/T]AAAAACAGGGAATGA | 9097 |
rs765261302 | in-del | -/TTTT | | | intron-variant | USP14 | GRCh38.p7 | 18:180212 | TTAATGATTTAATCC[-/TTTT]TTTTTTTTTTTTCCA | 9097 |
rs765297412 | snp | C/G | 4.97418e-05 | 0.00498682 | intron-variant | USP14 | GRCh38.p7 | 18:192941 | TTGATAGGAGTAAGA[C/G]ATTCTATTTTTCGCT | 9097 |
rs765408493 | in-del | -/AAAAATATATAT | | | intron-variant | USP14 | GRCh38.p7 | 18:171022 | CTTAAAAAAAAAAAA[-/AAAAATATATAT]ATATATATATATATA | 9097 |
rs765427514 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:174906 | TCAGCCTCCCGAGTA[A/G]CTGGGACTACAGGAA | 9097 |
rs765444021 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:210623 | AAGCCCCAAAGAGCT[A/T]TGGTTTATGAGGTTT | 9097 |
rs765474368 | in-del | -/TC | | | intron-variant | USP14 | GRCh38.p7 | 18:167928 | AATACAATTGATTTT[-/TC]TCTCTCTTTTTTTTT | 9097 |
rs765539882 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:190137 | TTATATTCATGCTAT[A/G]TAGTATAGTATTCCG | 9097 |
rs765556676 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:163239 | AACTGCCTAATTGGT[A/G]ATCTTCTAAGGGTCT | 9097 |
rs765590488 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:159323 | AACGTGGTGTGAGCT[G/T]TCAGAAGTAGATGAA | 9097 |
rs765644500 | snp | A/G | 3.53344e-05 | 0.00420309 | intron-variant | USP14 | GRCh38.p7 | 18:209945 | CCAAAATCATGATTT[A/G]AAATTAAACATTTTT | 9097 |
rs765672786 | snp | A/G | 1.64904e-05 | 0.00287139 | missense | USP14 | GRCh38.p7 | 18:163433 | AGACAGAAAGTTATG[A/G]TGAAAGGAGGAACGC | 9097 |
rs765722609 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:170844 | GGAGAACAGCACACA[C/T]GGGGGCCTGTCAGGC | 9097 |
rs765737827 | snp | C/G | 0.000150427 | 0.00867128 | synonymous-codon | USP14 | GRCh38.p7 | 18:199238 | AGAAGAAGAAGTCAC[C/G]AAAGGAAAGGAAAAT | 9097 |
rs765750972 | snp | C/T | 2.33724e-05 | 0.00341843 | intron-variant | USP14 | GRCh38.p7 | 18:178897 | AACATTACCAACTTT[C/T]AAGGATTTTCATGAA | 9097 |
rs765774070 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:184496 | TGATGGCTCACGCCT[A/G]TAATCCCAGTACTTT | 9097 |
rs765869416 | snp | A/G | 3.30273e-05 | 0.00406356 | synonymous-codon | USP14 | GRCh38.p7 | 18:202915 | CAAACAGTCTCCAAC[A/G]TTGCAAAGAAATGCC | 9097 |
rs765914478 | in-del | -/TG | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:211766 | AAGTGTTGCTCTCAT[-/TG]TGTGACTCAGTGCTG | 9097 |
rs765925853 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:193426 | TTTTTTTTACTCTCT[C/G]TCTAACAGCTTTATT | 9097 |
rs766045668 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:166561 | TGGTTTCGAACTCCT[A/G]ACCGCAGGTGATTTG | 9097 |
rs766174717 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:179113 | GTCTTTCAGAAAGTA[A/G]CATCTGAATGTCTTG | 9097 |
rs766193900 | in-del | -/C | 1.64841e-05 | 0.00287085 | intron-variant | USP14 | GRCh38.p7 | 18:192837 | CTCGGCTTTAATGTT[-/C]CTAGGTATGCAGGTG | 9097 |
rs766266096 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:187521 | GTTTGGGATAAATTG[A/G]CATTTTTGCAATATT | 9097 |
rs766287342 | in-del | -/AAATATATATAT | | | intron-variant | USP14 | GRCh38.p7 | 18:171024 | TAAAAAAAAAAAAAA[-/AAATATATATAT]ATATATATATATATA | 9097 |
rs766313488 | snp | C/T | 1.64757e-05 | 0.00287012 | missense | USP14 | GRCh38.p7 | 18:196694 | GTATTCCACCTATTA[C/T]TCTACTGCAGTTTTT | 9097 |
rs766315968 | snp | A/C | 1.74169e-05 | 0.00295096 | synonymous-codon | USP14 | GRCh38.p7 | 18:199307 | GTATCTTTTTACAGG[A/C]CTTAAATTGGTAAGG | 9097 |
rs766344901 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:205348 | GTGTTGACCTTGATG[C/G]AGTCAAAATACAGTA | 9097 |
rs766369983 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:201905 | GATATTTTATCTTTT[A/G]TTCTGATAATTCTTG | 9097 |
rs766514319 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:185726 | TTTTTGAGACAGGCC[C/T]TCGCTCTGTTGCCCA | 9097 |
rs766621306 | snp | G/T | 1.6516e-05 | 0.00287362 | missense | USP14 | GRCh38.p7 | 18:204640 | AAATGGTGTCTTTTC[G/T]ATCCAAATTCAAGGA | 9097 |
rs766668848 | snp | A/G | 4.90256e-05 | 0.0049508 | intron-variant | USP14 | GRCh38.p7 | 18:163294 | AATTAAAAAAATTGT[A/G]ATTTTGTTTGCAGTT | 9097 |
rs766733597 | snp | A/T | 1.65345e-05 | 0.00287524 | intron-variant | USP14 | GRCh38.p7 | 18:192925 | CTAAATATACTACTT[A/T]TTGATAGGAGTAAGA | 9097 |
rs766837535 | snp | A/G | 0.000302097 | 0.0122865 | intron-variant | USP14 | GRCh38.p7 | 18:198023 | ATTTATATAAAGTTG[A/G]AATTTTTATTTTAAT | 9097 |
rs766873547 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:192536 | TGCCATTGCACTCCA[A/G]CCTGGGCGACAAGAG | 9097 |
rs766924352 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:172627 | CTTCAGGAACCAGTG[A/C]CGTGATCAGTCAGTA | 9097 |
rs766966331 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:205486 | TTTTGTCATTTCAAG[A/G]AAGTTGGCCAGGCAT | 9097 |
rs767062944 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:171148 | ACAGTAAGTGCTGAT[A/G]GAGAAGCTGCAGTAA | 9097 |
rs767107056 | in-del | CTAGAGTGCAATGGCGCGATCTCGGCTC/GCGGG | | | intron-variant | USP14 | GRCh38.p7 | 18:167984 | CTCTTATTGCCCAGG[lengthTooLong]GCTGCAACCTCTGCC | 9097 |
rs767129486 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:201987 | AATGTTAAAAAGCTA[C/T]TCCACAGTGATTCCT | 9097 |
rs767165508 | snp | A/G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:177590 | CTAATTTTAATCATC[A/G/T]TCTGGATATTTTTAG | 9097 |
rs767243828 | in-del | -/GTGCAAATCAGGGCATGTAGTCGTTCTGCCATTGCACTGTC | 1.66758e-05 | 0.0028875 | intron-variant | USP14 | GRCh38.p7 | 18:203205 | GTTAGTAATGAACTT[lengthTooLong]TACTTTGTATAAGAA | 9097 |
rs767283593 | snp | A/G | 1.6713e-05 | 0.00289072 | intron-variant | USP14 | GRCh38.p7 | 18:180386 | GTTCACATTTGGATG[A/G]GTAGTATTGTTTTGT | 9097 |
rs767300860 | snp | A/T | 1.65045e-05 | 0.00287263 | splice-acceptor-variant | USP14 | GRCh38.p7 | 18:166785 | GTTTGTCTTTGAAAC[A/T]GGATGATGATTGGGG | 9097 |
rs767321960 | snp | A/G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:195542 | GAGGAGAAATGGTTC[A/G/T]AAATCCAAGAGAACA | 9097 |
rs767342857 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:177159 | ACATTTTTCTTGTTA[G/T]GCTTATTCTTAGATA | 9097 |
rs767350222 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:163563 | AAGTGCTTTTTTTAT[A/G]TGATGAGAGTATGTC | 9097 |
rs767397095 | snp | C/T | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212528 | AGAATTGCTTGAACC[C/T]GGAAGGCAGAAGTTG | 9097 |
rs767399745 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:173790 | TTATTTTTTTCACAT[C/G]AGTATTTAGTGAGCA | 9097 |
rs767421602 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:179586 | GGTTTTTTTTTTTGC[-/T]TTTTTTTTTTTTTTT | 9097 |
rs767446865 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:165960 | TGAGGGGAAAGGCCT[A/G]GCTGTAGTTAGTAAA | 9097 |
rs767484871 | snp | A/G | 4.95626e-05 | 0.00497784 | intron-variant | USP14 | GRCh38.p7 | 18:204739 | ATATCTTAATCTCCC[A/G]TCAGTGCTCAGCAAT | 9097 |
rs767498029 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:159568 | GTTACAGTTCCTTTA[C/T]TGAAGATTCAGCATT | 9097 |
rs767521310 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:210778 | GATTTACATTTTTAT[A/G]TCTTTCTGTTGTCTG | 9097 |
rs767559663 | in-del | -/CCAAAGC | | | intron-variant | USP14 | GRCh38.p7 | 18:197247 | CTCATGGCTCCAAGG[-/CCAAAGC]CTTAGGCTTTCCCTG | 9097 |
rs767583291 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:160553 | CACCTGTGCCTCTTA[C/T]AGAGTTAGGGTTTTG | 9097 |
rs767622773 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:172740 | AGCAATAAATTATTT[C/T]AAAATTAAGGTATGT | 9097 |
rs767636421 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:173300 | TTTTTTTTAGTAGAG[A/G]CGGGGTTTCACCATG | 9097 |
rs767773936 | in-del | -/TAAG | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214222 | GCTTGAAAGCACGAA[-/TAAG]TAAGTGAGAACAGAG | 9097 |
rs767805095 | snp | C/T | 1.65111e-05 | 0.0028732 | stop-gained | USP14 | GRCh38.p7 | 18:197646 | TGGATACAAATGATG[C/T]GAGTATTGCAACAGA | 9097 |
rs767824090 | snp | C/G | 1.66427e-05 | 0.00288462 | missense | USP14 | GRCh38.p7 | 18:204612 | GAACTGTGTACACCA[C/G]AACTTCAAGAGAAAA | 9097 |
rs767834796 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:187125 | TGAACTACTGTTTAC[C/T]CGTGAGTTTATTGGT | 9097 |
rs767849121 | in-del | -/ATG | | | intron-variant | USP14 | GRCh38.p7 | 18:187872 | AAACACATTTTAGTT[-/ATG]ATGATATTTATGATT | 9097 |
rs767855350 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:189749 | GCCTCCCAAGTGCTG[A/G]GATTACAGGCAAGAG | 9097 |
rs767858168 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:193904 | CAGTCGTGTACAAGT[C/T]TTGGTGTGGACAAAT | 9097 |
rs767895900 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:186072 | AAATAACAGAAAAGT[C/T]TACATATTTGATATT | 9097 |
rs767982260 | snp | A/G | 1.78828e-05 | 0.00299017 | intron-variant | USP14 | GRCh38.p7 | 18:211097 | TGAGACGAATCCTGC[A/G]TAACATTAATTCATC | 9097 |
rs768007853 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:173196 | TCACTGCAAGCTCCA[C/G]CTCCTGGTTCACGCC | 9097 |
rs768034681 | snp | C/T | 1.86572e-05 | 0.00305422 | utr-variant-5-prime | USP14 | GRCh38.p7 | 18:158682 | TCCTGCGCCGCCGCC[C/T]CCCGCCGCGCCCCGC | 9097 |
rs768036719 | snp | A/G | 2.90154e-05 | 0.00380878 | intron-variant | USP14 | GRCh38.p7 | 18:198002 | TGGAAGAAAATCTAC[A/G]TTAATATTTATATAA | 9097 |
rs768105781 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:159153 | GGTTGCCAAGCGGCG[G/T]TCGCCGCCCTTCGTC | 9097 |
rs768138290 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:205365 | GTCAAAATACAGTAC[A/T]TTTCCATCACCACAA | 9097 |
rs768139860 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:192671 | AGCATTCCTTTTTTT[C/G]TCCATATTTCTGGTC | 9097 |
rs768142911 | snp | A/G | 1.66349e-05 | 0.00288395 | intron-variant | USP14 | GRCh38.p7 | 18:196617 | TGTTTTACTAAGGCA[A/G]TGTTTGCTTTGTCTT | 9097 |
rs768160862 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:172299 | AATTGCCACAATCTC[A/G]TGATACAACTTGAAC | 9097 |
rs768173975 | snp | C/T | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212363 | TGTAATCCCAGCACT[C/T]TGGGAGGCTGAGGCA | 9097 |
rs768188788 | in-del | -/TGT | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214077 | GCTCCTTAGCTTTGC[-/TGT]TGTTATAGTGTAGCT | 9097 |
rs768195855 | snp | G/T | 3.29582e-05 | 0.00405931 | missense | USP14 | GRCh38.p7 | 18:192861 | GCAGGTGCCTTGAGA[G/T]CTTCAGGGGAAATGG | 9097 |
rs768334602 | snp | A/T | 1.66026e-05 | 0.00288115 | intron-variant | USP14 | GRCh38.p7 | 18:163469 | GTAAAATGTAGTCCA[A/T]ATTTTCATCACATTA | 9097 |
rs768365802 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:166772 | TTAAATGTCTTTTGT[G/T]TGTCTTTGAAACAGG | 9097 |
rs768471673 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:193077 | CCAGATTATAAATCA[A/G]TGATGTCTGTCGTTT | 9097 |
rs768499881 | snp | C/T | 1.65111e-05 | 0.0028732 | intron-variant | USP14 | GRCh38.p7 | 18:204718 | ACTGCTGACTTTATA[C/T]TCTTAATATCTTAAT | 9097 |
rs768572734 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:178578 | TTAGAAGTTTCATCA[C/T]GAAAAAGTTTCTTTG | 9097 |
rs768809397 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:176080 | TTTCGTTTTCCTCTC[A/T]AGTATTGGCAAATTA | 9097 |
rs768813282 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:169398 | GAGTGGACATCTTGT[C/T]TTATTCTAGTTCACT | 9097 |
rs768868525 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:174478 | ACCATGTTGGTCAGG[C/T]TGGTCTCAAACTCCT | 9097 |
rs768876098 | in-del | -/AGGTTAACAG | | | intron-variant | USP14 | GRCh38.p7 | 18:202402 | TTTCCCACATCTGTT[-/AGGTTAACAG]AGGTTTCTGTGTTAT | 9097 |
rs768899664 | snp | A/G | 1.6495e-05 | 0.0028718 | missense | USP14 | GRCh38.p7 | 18:198101 | AAGAAAAGTTTAATC[A/G]ATCAGTTCTTCGGTG | 9097 |
rs768971826 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:202758 | TGGTATAAACCCATT[G/T]ATGTACTGTATATTG | 9097 |
rs769049229 | snp | A/G | 3.15981e-05 | 0.00397467 | intron-variant | USP14 | GRCh38.p7 | 18:204527 | TAAATATCTTTATAA[A/G]TGTGTTTACACATGT | 9097 |
rs769067838 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:184389 | CACGAGAGGTGTTTT[A/G]CAGCTGGAGATGAGG | 9097 |
rs769194685 | snp | C/T | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213579 | CCACTCACACCGAGG[C/T]CATCATCTCAACATT | 9097 |
rs769258728 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:206783 | GTGCGGACCTATAAT[C/T]CCAGCTACTTGGGAG | 9097 |
rs769268110 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:179354 | TATGTTCCTGGCAGA[C/T]AGTACTATATAAGTA | 9097 |
rs769279664 | snp | A/G | 1.65811e-05 | 0.00287929 | intron-variant | USP14 | GRCh38.p7 | 18:180361 | CTGCAGTCTTTTTTG[A/G]GTAAGGGATGTTCAC | 9097 |
rs769282071 | snp | A/G | 1.65064e-05 | 0.00287279 | intron-variant | USP14 | GRCh38.p7 | 18:204703 | ATACAGTAGGTTCTT[A/G]CTGCTGACTTTATAC | 9097 |
rs769293670 | snp | C/T | 4.94866e-05 | 0.00497402 | missense | USP14 | GRCh38.p7 | 18:180314 | TGTATTCGTTCTGTG[C/T]CTGAACTCAAAGATG | 9097 |
rs769303509 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:160196 | GTAATCCCAGCTACT[A/G]GGGAGGCTGAGGCAG | 9097 |
rs769405044 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:161350 | ATCTTAGAACACACC[A/G]TGCTGCTTTATGCTG | 9097 |
rs769461052 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:193198 | GGGGATAGCCAGCGA[C/T]GGGTTTTATCATAAT | 9097 |
rs769505016 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:207506 | CAACATGGCAAAACC[C/G]TGTCTCCACAAAAAA | 9097 |
rs769706587 | snp | C/T | 1.69421e-05 | 0.00291046 | intron-variant | USP14 | GRCh38.p7 | 18:210517 | TATTCTTTTTTCAAC[C/T]GTTCAATATTATTTT | 9097 |
rs769706876 | snp | C/G | 1.99455e-05 | 0.00315791 | intron-variant | USP14 | GRCh38.p7 | 18:158748 | TCGCGCGCAGCACAC[C/G]GGACCGGCGCTAGGC | 9097 |
rs769741087 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:189600 | TGATTCTCCTACCAC[A/C]GCCTCCTGAGTAGCT | 9097 |
rs769769686 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:167685 | TAATTAATTAATTTT[A/C]ATTATTTTTTGTAGA | 9097 |
rs769780873 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:177703 | GTGTTCATGCCTTCC[A/G]ATTAAGATACTGAGT | 9097 |
rs769784640 | snp | C/T | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213646 | GGTTAGGCCTAAGAG[C/T]GTTTACCGAATAATC | 9097 |
rs769859580 | snp | A/G | 1.66991e-05 | 0.00288951 | synonymous-codon | USP14 | GRCh38.p7 | 18:163351 | TGAAGGTGTAGAATT[A/G]AATACAGATGAACCT | 9097 |
rs769885274 | in-del | -/A | 4.96208e-05 | 0.00498076 | intron-variant | USP14 | GRCh38.p7 | 18:198177 | CTCATACCTTATTAG[-/A]AATTGGCATAAATAG | 9097 |
rs769902319 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:194276 | AAGTTTTTAGTGAGA[A/G]AGTGTGATCATTTAT | 9097 |
rs769938154 | in-del | -/A | 6.74218e-05 | 0.00580572 | intron-variant | USP14 | GRCh38.p7 | 18:210346 | AGAAGGCACATGTCT[-/A]TTCATTGTCTAATAT | 9097 |
rs769955385 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:165899 | AGCATATTGGGTACC[C/T]GATACCTTCTATAAA | 9097 |
rs769984105 | in-del | -/TT | | | intron-variant | USP14 | GRCh38.p7 | 18:174270 | CACGTTTTTCTTTCT[-/TT]TTTTTTTTTTTTTTG | 9097 |
rs770001146 | snp | G/T | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212269 | TGATGTTATCAGTCA[G/T]ATTCTTTCCTTGGCT | 9097 |
rs770008421 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:164602 | GGGATTACAGGTGTC[C/T]ACCACCATGCCCGGC | 9097 |
rs770086365 | in-del | -/ATC | | | intron-variant | USP14 | GRCh38.p7 | 18:193206 | CCAGCGACGGGTTTT[-/ATC]ATAATCCATGTATCA | 9097 |
rs770149327 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:186837 | TGTATGTGTTTTTTT[A/G]TAACCAATTCAAACA | 9097 |
rs770194692 | in-del | -/TGAT | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214002 | TAGATAGATAGATGA[-/TGAT]TGATTGATTGATGAT | 9097 |
rs770243555 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:197437 | GCTCAGCAGATGTCT[C/G]TTGAATGAATAAGCT | 9097 |
rs770269361 | snp | A/G | 1.72089e-05 | 0.00293328 | intron-variant | USP14 | GRCh38.p7 | 18:202848 | AAAATTTTTAAAACT[A/G]ATGTTTGGTCTTCTG | 9097 |
rs770338034 | snp | G/T | 1.66504e-05 | 0.0028853 | intron-variant | USP14 | GRCh38.p7 | 18:166867 | GCAGTAACCTCATTA[G/T]GATACCAAAATACAT | 9097 |
rs770454953 | snp | G/T | 3.31296e-05 | 0.00406985 | intron-variant | USP14 | GRCh38.p7 | 18:203050 | AAATAATTAAAACTT[G/T]TATGGTATTTTGATG | 9097 |
rs770525635 | snp | G/T | 2.17059e-05 | 0.00329431 | intron-variant | USP14 | GRCh38.p7 | 18:204555 | TGTTTTTTGTTTGTT[G/T]GTATATAGGATGTTA | 9097 |
rs770527569 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:209877 | GTCTCTGTGCACTGT[A/T]GACAGTAAATATTTA | 9097 |
rs770547489 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:162727 | ATTGTTGGAGTAGGA[G/T]TCAGAAGACTTGGGA | 9097 |
rs770561273 | in-del | -/TC | | | intron-variant | USP14 | GRCh38.p7 | 18:193083 | TATAAATCAATGATG[-/TC]TGTCGTTTGTGAAAA | 9097 |
rs770573718 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:183109 | CTTACTGTGTCTTTT[A/G]TATATATCCCAAAAT | 9097 |
rs770585056 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:208212 | ATTCAAATGATCTAT[C/T]TCATATTGTGTTTGT | 9097 |
rs770610018 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:210381 | GGATTTACATCTTTC[C/T]TTAGATATTGGCTCC | 9097 |
rs770652577 | in-del | -/TGA | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214011 | TAGATGATGATTGAT[-/TGA]TGATTGATAGTAAAT | 9097 |
rs770696551 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:194494 | CCAGTTACTAACTTT[C/T]AGTCGCATTTGGTTT | 9097 |
rs770741970 | snp | A/G | | | missense | USP14 | GRCh38.p7 | 18:204629 | ACTTCAAGAGAAAAT[A/G]GTGTCTTTTCGATCC | 9097 |
rs770749470 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:193450 | CTTTATTGATATAGT[A/G]TACATATCATAAAAT | 9097 |
rs770909909 | snp | C/T | 1.66181e-05 | 0.00288249 | intron-variant | USP14 | GRCh38.p7 | 18:166859 | ATTATAATGCAGTAA[C/T]CTCATTATGATACCA | 9097 |
rs770939713 | snp | C/G | 0.00193798 | 0.0310682 | intron-variant | USP14 | GRCh38.p7 | 18:158734 | GCCCTGTCCTGGCCT[C/G]GCGCGCAGCACACCG | 9097 |
rs770962247 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:169984 | TATTCCCTGAGACAA[C/G]ACAGTATTGAAATTA | 9097 |
rs770967279 | snp | A/C | 1.75164e-05 | 0.00295937 | intron-variant | USP14 | GRCh38.p7 | 18:202834 | TATATTGCAGAAATA[A/C]AATTTTTAAAACTAA | 9097 |
rs770994651 | snp | A/G | 1.66026e-05 | 0.00288115 | intron-variant | USP14 | GRCh38.p7 | 18:197706 | AAAGAGGTAATTGAA[A/G]TATATTTGTGATTAT | 9097 |
rs771088547 | snp | A/G | 6.60742e-05 | 0.00574741 | intron-variant | USP14 | GRCh38.p7 | 18:166750 | TGTTCAGCTTGTACA[A/G]TGGTGGTTAAATGTC | 9097 |
rs771124954 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:197779 | CCTCAAAGGCTTAAA[A/G]TAAGTTCCATCTTAT | 9097 |
rs771244482 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:161457 | ATTCAAAATTGATAG[A/T]GATAACTCAGAAGTT | 9097 |
rs771300007 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:160291 | TCTGGGTGAAAAAAG[C/T]GAAACTGGGTCTCAA | 9097 |
rs771305270 | snp | C/T | 1.68408e-05 | 0.00290175 | intron-variant | USP14 | GRCh38.p7 | 18:210055 | CATTCTCATTTTAAT[C/T]GAGTTATTGTATGTG | 9097 |
rs771342011 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:173434 | CTGTTTTTTTGAGAC[A/G]GAGTTCCGTTCTTGT | 9097 |
rs771342391 | snp | A/G | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:213889 | CAGGCAATTTTTGTA[A/G]GGCTAGAAGGAAAAG | 9097 |
rs771347794 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:208900 | ACAGGCGAGTGCCAC[C/T]ATGCCTGGCTAATTT | 9097 |
rs771468582 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:188398 | ATTCCTGATACATTC[A/G]TATTCTTTCAATATA | 9097 |
rs771503221 | snp | C/G | 1.67683e-05 | 0.00289549 | missense | USP14 | GRCh38.p7 | 18:199227 | ACAGAATCTGAAGAA[C/G]AAGAAGTCACCAAAG | 9097 |
rs771529647 | in-del | -/TTATC | 1.65611e-05 | 0.00287755 | intron-variant | USP14 | GRCh38.p7 | 18:166827 | TAAAAAATGTAAGTA[-/TTATC]TTATGAACGTTTATT | 9097 |
rs771610285 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:201090 | ATAGGAATGAGCCAC[C/T]GTGCCCAGCCAGGAT | 9097 |
rs771615143 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:184065 | GAGTTCTGTGTAAGC[A/G]GGGGAGATTTCATCC | 9097 |
rs771663372 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:172224 | ATCTGAGTGACAGAG[C/T]GAGACCCTGTATCTA | 9097 |
rs771664882 | snp | C/T | 3.38381e-05 | 0.00411314 | intron-variant | USP14 | GRCh38.p7 | 18:197570 | GAAGAACTTTGTAGA[C/T]CATTCACTGCCAGGA | 9097 |
rs771665486 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157069 | GACCCTGTCTCAAAA[C/G]AAACAAACAAAACTT | 9097 |
rs771674496 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:196024 | CAAAGAGTAGATACA[C/T]TTAAAAATGTTTAAG | 9097 |
rs771777117 | snp | A/T | 1.65162e-05 | 0.00287365 | missense | USP14 | GRCh38.p7 | 18:202905 | AAGAAATCACCAAAC[A/T]GTCTCCAACGTTGCA | 9097 |
rs771803601 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:183342 | TTTTTTCTTTCCCCC[A/G]GTTTTCCAAGAATGT | 9097 |
rs771853977 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:191815 | AATTTTGATTTTAGT[A/C]ACTCTAATGGGTGTG | 9097 |
rs771893364 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:205859 | AGCATAATTCTCTGG[C/T]GACTCATCCAGGGTG | 9097 |
rs771938055 | snp | A/G | 1.64833e-05 | 0.00287078 | synonymous-codon | USP14 | GRCh38.p7 | 18:196668 | TGATTCCATGGATAA[A/G]ACTTCTTCCAGTATT | 9097 |
rs771988642 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:190865 | CAGTGTTAATGTTAT[G/T]TGGCTTAATGGATGG | 9097 |
rs772001081 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:210797 | TTCTGTTGTCTGGCT[C/T]AAATAGGAGGCAGCT | 9097 |
rs772121571 | snp | C/T | 2.20276e-05 | 0.00331863 | intron-variant | USP14 | GRCh38.p7 | 18:199170 | AACAAATTGAATACC[C/T]GTTGGCATATTCCTT | 9097 |
rs772127850 | snp | A/G | 4.94825e-05 | 0.00497381 | synonymous-codon | USP14 | GRCh38.p7 | 18:163381 | TCCAATGGTATTCAA[A/G]GCTCAGCTGTTTGCG | 9097 |
rs772163773 | snp | A/G | 1.64906e-05 | 0.00287142 | missense | USP14 | GRCh38.p7 | 18:210442 | GTACTAACACACCAG[A/G]GAAGGTCTAGTTCTT | 9097 |
rs772229388 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:192148 | AATGCTGAATGTAGG[C/T]GTATGATTTTTGATT | 9097 |
rs772289272 | snp | A/G | 3.34907e-05 | 0.00409197 | intron-variant | USP14 | GRCh38.p7 | 18:163490 | CATCACATTACTATT[A/G]TTGTATACTTTTTGA | 9097 |
rs772414124 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:201335 | ATTGGAATAGGTCCT[C/G]TGTGCAGAGGCCTAG | 9097 |
rs772440015 | in-del | -/A | | | intron-variant | USP14 | GRCh38.p7 | 18:169361 | GCAAGACTCTACCTC[-/A]AAAAAAAAAAAAAAA | 9097 |
rs772460156 | snp | C/G | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:211734 | TAACAAACATTTTTC[C/G]AGGAAGGTGGAAAAG | 9097 |
rs772467403 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:199702 | CTTCAGTTGGGCCTG[C/T]GTTGCACTGTTGGCT | 9097 |
rs772506851 | snp | C/T | 1.66308e-05 | 0.00288359 | synonymous-codon | USP14 | GRCh38.p7 | 18:210024 | TGAACCCTTTTCTTT[C/T]GCTGATGGTAAGTAA | 9097 |
rs772512726 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:194798 | TAGCCGGGTGTGTTG[A/G]TGCATGTCTGTAATC | 9097 |
rs772538491 | in-del | -/C | 4.12099e-05 | 0.00453908 | intron-variant | USP14 | GRCh38.p7 | 18:179085 | CTACTTTTTGAAGGA[-/C]CATTATTAAGGTGTC | 9097 |
rs772677054 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:207829 | CTAAATAGTTTATTC[-/T]TTTTGATGCTTTTGT | 9097 |
rs772735287 | in-del | -/TTG | | | intron-variant | USP14 | GRCh38.p7 | 18:183764 | TTTTTTTTTTTTTCC[-/TTG]TTGTTTGGCCTTTTA | 9097 |
rs772758705 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:173316 | CGGGGTTTCACCATG[-/T]TAGCCAGGATGGTCT | 9097 |
rs772787316 | snp | C/T | 3.30295e-05 | 0.0040637 | missense | USP14 | GRCh38.p7 | 18:202910 | ATCACCAAACAGTCT[C/T]CAACGTTGCAAAGAA | 9097 |
rs772812026 | in-del | -/TGA | | | cds-indel | USP14 | GRCh38.p7 | 18:212897 | GGCAGAGCACAACAC[-/TGA]TGATAACTATTAAAA | 9097 |
rs772874074 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:179050 | GCTGTAAGACACACC[A/C]GATTTTATGTGTTTG | 9097 |
rs772877511 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:202798 | TAGTGCTAGTTTTTA[A/G]AAGGCTTACTGGTGT | 9097 |
rs772910121 | snp | C/T | 9.92589e-05 | 0.00704412 | intron-variant | USP14 | GRCh38.p7 | 18:203069 | GGTATTTTGATGTAA[C/T]GGGATTTCTTTACAT | 9097 |
rs772916690 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:160219 | TGAGGCAGGAGAATC[G/T]CTTGAACCTGTGAAG | 9097 |
rs772951851 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:193221 | ATCATAATCCATGTA[C/T]CATTATAAAAGAGGG | 9097 |
rs772996713 | snp | A/C | 4.97475e-05 | 0.00498711 | intron-variant | USP14 | GRCh38.p7 | 18:178892 | ACATAAACATTACCA[A/C]CTTTTAAGGATTTTC | 9097 |
rs772997170 | snp | C/G | 3.38903e-05 | 0.00411631 | intron-variant | USP14 | GRCh38.p7 | 18:197571 | AAGAACTTTGTAGAT[C/G]ATTCACTGCCAGGAT | 9097 |
rs773003116 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:208784 | TGAGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG | 9097 |
rs773014517 | snp | A/C/G | 0.000148309 | 0.00861012 | missense | USP14 | GRCh38.p7 | 18:196679 | ATAAAACTTCTTCCA[A/C/G]TATTCCACCTATTAT | 9097 |
rs773044651 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:175933 | AAATGTAGGACTATT[A/T]AGATATTATGTTTTC | 9097 |
rs773046567 | in-del | -/TGTG | | | intron-variant | USP14 | GRCh38.p7 | 18:179541 | TTTTTAACACCTAGC[-/TGTG]ATTTATTTAGTGCCA | 9097 |
rs773085124 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:167795 | TGCTGGGATTAACAG[A/G]TGTGAGTCACTGTGC | 9097 |
rs773133024 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:191758 | CAGTAATTCTGATTG[C/T]TCCACAATCTTGCCG | 9097 |
rs773184132 | in-del | -/AGAT/AGATAGATAGAC | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:213984 | ATAGATTAGATAGAT[-/AGAT/AGATAGATAGAC]AGATAGATAGATAGA | 9097 |
rs773222923 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:167108 | AAAAAAATTAGCTGG[C/G]TGTGGTGGTGCACGC | 9097 |
rs773237621 | in-del | -/TTTA | 1.82891e-05 | 0.00302394 | intron-variant | USP14 | GRCh38.p7 | 18:199193 | TATTCCTTATCTTAG[-/TTTA]CAAAGCATGAAATGT | 9097 |
rs773335424 | snp | A/C | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212273 | GTTATCAGTCAGATT[A/C]TTTCCTTGGCTCAGT | 9097 |
rs773356989 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:203616 | TAGGTGGTTTCTTTC[-/T]TTTTTTTTTTTGAGA | 9097 |
rs773427527 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:172758 | AATTAAGGTATGTGC[A/G]TTCCTTTTTAGACAT | 9097 |
rs773551473 | snp | C/T | 1.65255e-05 | 0.00287445 | intron-variant | USP14 | GRCh38.p7 | 18:204741 | ATCTTAATCTCCCAT[C/T]AGTGCTCAGCAATTA | 9097 |
rs773555852 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:186844 | GTTTTTTTATAACCA[A/G]TTCAAACAGTCTTAA | 9097 |
rs773634444 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:198463 | CTGGTATTGAACTCC[C/T]GACTTTAGTTGATCT | 9097 |
rs773637527 | in-del | -/TTG | | | intron-variant | USP14 | GRCh38.p7 | 18:176790 | TAAATCTTTAATTAA[-/TTG]TTGTTGTGGTATGGT | 9097 |
rs773654673 | snp | A/G | 1.64936e-05 | 0.00287168 | missense | USP14 | GRCh38.p7 | 18:211222 | GGAGACTGGCATATC[A/G]CTTACGTTCTACTCT | 9097 |
rs773749891 | snp | C/T | 1.66275e-05 | 0.00288331 | intron-variant | USP14 | GRCh38.p7 | 18:196618 | GTTTTACTAAGGCAA[C/T]GTTTGCTTTGTCTTT | 9097 |
rs773787994 | in-del | -/AAA | | | intron-variant | USP14 | GRCh38.p7 | 18:169361 | GCAAGACTCTACCTC[-/AAA]AAAAAAAAAAAAAAA | 9097 |
rs773809163 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:183622 | TTTACTGATTCATAC[A/G]TCTACTTTGTTTCAC | 9097 |
rs774021914 | snp | A/G | 1.66849e-05 | 0.00288828 | synonymous-codon | USP14 | GRCh38.p7 | 18:204608 | GTATGAACTGTGTAC[A/G]CCAGAACTTCAAGAG | 9097 |
rs774104315 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:190669 | AAAATGTCCTCTCTT[G/T]GTAGGTGTCAAAGTA | 9097 |
rs774108982 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:183262 | ATGCTTACTGATGAG[A/G]GGTCTGATATCAGTC | 9097 |
rs774128357 | in-del | -/TAT | 0.000152095 | 0.0087192 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:211296 | TAATCTTCATTTTAG[-/TAT]TATTTATGCTTAGAT | 9097 |
rs774143424 | snp | A/G | 1.66963e-05 | 0.00288927 | synonymous-codon | USP14 | GRCh38.p7 | 18:199244 | AGAAGTCACCAAAGG[A/G]AAGGAAAATCAACTT | 9097 |
rs774164703 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:174919 | TAGCTGGGACTACAG[A/G]AATGTGCCACCACGC | 9097 |
rs774186118 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:210637 | TTTGGTTTATGAGGT[G/T]TGCCTCTCTTAATAC | 9097 |
rs774192136 | in-del | -/GAAGAA | 1.68643e-05 | 0.00290376 | cds-indel | USP14 | GRCh38.p7 | 18:199221 | AAATGTACAGAATCT[-/GAAGAA]GAAGAAGTCACCAAA | 9097 |
rs774225294 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:189889 | ACCCAAAATAAAGGC[A/C]GAACCCTTCTAGCAC | 9097 |
rs774275744 | snp | A/G | 8.49567e-05 | 0.00651699 | intron-variant | USP14 | GRCh38.p7 | 18:203240 | AATTCTTTGAAGGTA[A/G]TTGCTAACTCACAAT | 9097 |
rs774286504 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157022 | GTGAGCCGTAATTGC[A/G]TCACTGCACTCCAGC | 9097 |
rs774389840 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:185770 | CACGATCACAGATCA[C/T]TGCAGCCTTGACCTC | 9097 |
rs774408496 | snp | A/G | 0.000280822 | 0.0118462 | missense | USP14 | GRCh38.p7 | 18:163370 | ACAGATGAACCTCCA[A/G]TGGTATTCAAGGCTC | 9097 |
rs774420933 | snp | C/T | 1.98754e-05 | 0.00315235 | intron-variant | USP14 | GRCh38.p7 | 18:197746 | TTATACCTTGATTTT[C/T]TTTTTTATTTTTTTT | 9097 |
rs774441789 | snp | G/T | 1.67407e-05 | 0.00289311 | intron-variant | USP14 | GRCh38.p7 | 18:163275 | TCTTGTCTTGTTATT[G/T]TTTAATTAAAAAAAT | 9097 |
rs774462350 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:187053 | ATGCTACATTCTGTA[C/T]ATATTCATCAATGTA | 9097 |
rs774499646 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:170049 | GCTCACACCTGTAAT[C/G]CTAGCACTTTGGGAG | 9097 |
rs774503287 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:166136 | CTCTGCTGGTTCCAA[A/G]CATCCAAAAAATAGG | 9097 |
rs774577050 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:193505 | ATTGTTTTTTAGTTT[A/G]TCCACAGAGTTGTGC | 9097 |
rs774652379 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:173473 | CTGGAGTGCAATGGC[A/G]TGATCTCAGCTCACC | 9097 |
rs774661451 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:199560 | TTTAAAAAAAAATTT[C/G]TGCTTTTTGTTGGTT | 9097 |
rs774674160 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:201522 | TCACGCTCTGTCTTA[A/T]GATACCGAGGGGAGA | 9097 |
rs774679565 | in-del | -/AA | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:213858 | ATCCCTGAAGTGATT[-/AA]AAGTCTTGAGAGGTC | 9097 |
rs774716437 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:197819 | TGTATTTAAATACTT[C/T]AGATGCTCAATCTGT | 9097 |
rs774718805 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:161546 | CCTTTGTAATACTTA[C/G]ATAGTTAATTACTCT | 9097 |
rs774770689 | snp | A/C | 1.79913e-05 | 0.00299922 | intron-variant | USP14 | GRCh38.p7 | 18:209938 | TTTATTTCCAAAATC[A/C]TGATTTAAAATTAAA | 9097 |
rs774774395 | in-del | -/C | | | intron-variant | USP14 | GRCh38.p7 | 18:198703 | CTTTAGCAGAGTCTA[-/C]CTCATTTTCATTCAC | 9097 |
rs774825018 | snp | A/G | 3.29864e-05 | 0.00406105 | missense | USP14 | GRCh38.p7 | 18:211219 | GGTGGAGACTGGCAT[A/G]TCGCTTACGTTCTAC | 9097 |
rs774854795 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:205036 | TGCGCCACCATGCCC[A/G]GCTATTTTTTTGTAT | 9097 |
rs774871774 | snp | A/G | 0.000400153 | 0.0141392 | intron-variant | USP14 | GRCh38.p7 | 18:179047 | TCTGCTGTAAGACAC[A/G]CCAGATTTTATGTGT | 9097 |
rs774923399 | in-del | -/AGAA | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:213996 | GATAGATAGATAGAT[-/AGAA]AGATGATGATTGATT | 9097 |
rs774939840 | snp | A/G | 1.64817e-05 | 0.00287064 | missense | USP14 | GRCh38.p7 | 18:192844 | TTAATGTTCCTAGGT[A/G]TGCAGGTGCCTTGAG | 9097 |
rs774943013 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:161348 | ACATCTTAGAACACA[C/T]CATGCTGCTTTATGC | 9097 |
rs774994938 | snp | G/T | 1.65078e-05 | 0.00287291 | intron-variant | USP14 | GRCh38.p7 | 18:204708 | GTAGGTTCTTACTGC[G/T]GACTTTATACTCTTA | 9097 |
rs775110052 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:203659 | CTGTCACCCAGGCTG[G/T]AGTGCAGTGGCGCTA | 9097 |
rs775119976 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:201726 | TTGGCAGGGACTCTC[C/T]AGGATGGTATTTTCT | 9097 |
rs775227727 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:176179 | AAAAAACATTTGGCC[-/T]GTTCATTTATTACTT | 9097 |
rs775331169 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:164773 | TTTTTCTAAACAGTA[A/G]TTGTTACCTAACTCC | 9097 |
rs775363226 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:191892 | TCACTTCAGTGTTTG[A/T]TATTAACTGAATGAT | 9097 |
rs775365484 | in-del | -/CT | 0.000120214 | 0.00775194 | intron-variant | USP14 | GRCh38.p7 | 18:211122 | TTCATCTTCTTGTCC[-/CT]GTTATTTAGATGAAT | 9097 |
rs775404180 | snp | A/G | 1.70075e-05 | 0.00291607 | missense | USP14 | GRCh38.p7 | 18:204591 | CCTCTTATGTTGGAT[A/G]TGTATGAACTGTGTA | 9097 |
rs775407910 | snp | A/T | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:213975 | GACAAGATAGATAGA[A/T]TAGATAGATAGATAG | 9097 |
rs775416322 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:190917 | CATTTTATTGCTCTA[A/G]TATGGGAATTTTTTT | 9097 |
rs775473299 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:204905 | TGTGTTTTATTTTCC[-/T]TTTTTTTTTTTTGTG | 9097 |
rs775590577 | snp | A/G | 1.65902e-05 | 0.00288008 | intron-variant | USP14 | GRCh38.p7 | 18:197609 | TTTGTCTTTTTTTAC[A/G]TTACAGGATGCTAAT | 9097 |
rs775591277 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:201430 | TGATTTGTTATCTGG[A/G]GGCTCTCATCTATAG | 9097 |
rs775645982 | snp | C/T | 5.52929e-05 | 0.0052577 | intron-variant | USP14 | GRCh38.p7 | 18:210542 | TATTTTAACAGTTCA[C/T]TTATTATAAATTTTA | 9097 |
rs775683429 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:183349 | TTTCCCCCAGTTTTC[C/G]AAGAATGTGAGACTG | 9097 |
rs775687957 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:192218 | TCAGAGATTGTGTTA[G/T]TTTATTTTCTTTGTA | 9097 |
rs775789741 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:204285 | GATGTTTCTTTTCTC[A/G]GGTAAATTTTGGTAC | 9097 |
rs775804626 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:196046 | ATGTTTAAGCAGCTG[C/G]GTGTGGTGGCTCACA | 9097 |
rs775812353 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:188581 | GTCTATCTTTTCCTG[A/G]AACTTTTATTTTCTT | 9097 |
rs775816253 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:196605 | TAAATATGTGACTGT[G/T]TTACTAAGGCAATGT | 9097 |
rs775945149 | in-del | -/C | 3.86511e-05 | 0.00439591 | intron-variant | USP14 | GRCh38.p7 | 18:180210 | GTTTAATGATTTAAT[-/C]CTTTTTTTTTTTTTT | 9097 |
rs775949347 | snp | G/T | 2.98788e-05 | 0.00386504 | intron-variant | USP14 | GRCh38.p7 | 18:178865 | CTTTTGTTCCTGGCT[G/T]CTTTTGGTTTGACAT | 9097 |
rs775951116 | snp | A/G | 2.08509e-05 | 0.00322878 | intron-variant | USP14 | GRCh38.p7 | 18:179087 | ACTTTTTGAAGGACC[A/G]TTATTAAGGTGTCTT | 9097 |
rs775984763 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:210284 | TATTGGATTCTGATA[A/T]TACTTTCGTAATGTG | 9097 |
rs775995479 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:173599 | TGTATTTTTTTTAGT[A/G]TGTTGTTGGTCAGAC | 9097 |
rs776000756 | snp | A/T | 1.6666e-05 | 0.00288664 | intron-variant | USP14 | GRCh38.p7 | 18:202866 | GTTTGGTCTTCTGTT[A/T]TGTTCTTTCTTAGCG | 9097 |
rs776074529 | snp | A/T | 2.07799e-05 | 0.00322328 | intron-variant | USP14 | GRCh38.p7 | 18:204558 | TTTTTGTTTGTTTGT[A/T]TATAGGATGTTAAAT | 9097 |
rs776081635 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:206733 | GGTGAAACCCTGTCT[C/G]TACTAAAAATACAAA | 9097 |
rs776111042 | snp | C/T | 1.75459e-05 | 0.00296186 | intron-variant, missense | USP14 | GRCh38.p7 | 18:179033 | AAGAACAGTTAGCAT[C/T]TGCTGTAAGACACAC | 9097 |
rs776128176 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:161818 | GTTTTAAAAATATAT[A/G]TTTCAAAAGTTAGCT | 9097 |
rs776194587 | in-del | -/AGAG/AGATAGATAGAA | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:213988 | ATTAGATAGATAGAT[-/AGAG/AGATAGATAGAA]AGATAGATAGATGAT | 9097 |
rs776205396 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:174450 | TTTGTATTTTTAGTA[C/G]AGACGGGGTGTCACC | 9097 |
rs776295923 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:191183 | CTAAAATGTCTTAAC[A/G]GGGAAATGTAATGAT | 9097 |
rs776312246 | snp | C/G | 1.65526e-05 | 0.00287681 | intron-variant | USP14 | GRCh38.p7 | 18:180353 | AGGTAAGACTGCAGT[C/G]TTTTTTGGGTAAGGG | 9097 |
rs776380279 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:202496 | AAACGTAAAGAACAG[A/G]AGTTTCTTGGGCTCT | 9097 |
rs776507717 | in-del | -/GTTTC | | | intron-variant | USP14 | GRCh38.p7 | 18:209196 | TATGTTTTTAAATGT[-/GTTTC]TTTGTATAGTTTTTT | 9097 |
rs776563606 | snp | A/G/T | 1.65993e-05 | 0.00288086 | intron-variant | USP14 | GRCh38.p7 | 18:180369 | TTTTTTGGGTAAGGG[A/G/T]TGTTCACATTTGGAT | 9097 |
rs776578338 | snp | G/T | 1.66377e-05 | 0.00288419 | intron-variant | USP14 | GRCh38.p7 | 18:197603 | ACTTACTTTGTCTTT[G/T]TTTACATTACAGGAT | 9097 |
rs776624526 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:210519 | TTCTTTTTTCAACTG[A/T]TCAATATTATTTTAA | 9097 |
rs776626533 | in-del | -/A | | | intron-variant | USP14 | GRCh38.p7 | 18:177423 | TGAGTCCCTGTCTCT[-/A]AAAAAAAAAAAAAAA | 9097 |
rs776686515 | snp | A/G | 0.000125149 | 0.0079094 | intron-variant | USP14 | GRCh38.p7 | 18:158737 | CTGTCCTGGCCTCGC[A/G]CGCAGCACACCGGAC | 9097 |
rs776732794 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:189716 | TCGATCTCTTGACCT[C/G]GTGATCCACCTGCCT | 9097 |
rs776768515 | snp | A/C | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212128 | GTACAATTTCTGAAG[A/C]TGGTTATTAACACTG | 9097 |
rs776814532 | snp | A/T | 0.000150682 | 0.00867861 | missense | USP14 | GRCh38.p7 | 18:199231 | AATCTGAAGAAGAAG[A/T]AGTCACCAAAGGAAA | 9097 |
rs776833468 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:163075 | GCCACCACGCCCAGC[C/T]TGCTGAAGTCTCAGT | 9097 |
rs776871104 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:174271 | ACGTTTTTCTTTCTT[-/T]TTTTTTTTTTTTTTG | 9097 |
rs776954768 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:174737 | ACCCTCCTGAGTAGT[G/T]GGGACTATAGGCATG | 9097 |
rs776957672 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:185264 | TCCCGGCTTGAGCAA[G/T]TCTTCTGTCTCAGCC | 9097 |
rs776965296 | snp | C/T | 1.68746e-05 | 0.00290466 | intron-variant | USP14 | GRCh38.p7 | 18:210059 | CTCATTTTAATTGAG[C/T]TATTGTATGTGGGTC | 9097 |
rs777041276 | in-del | -/A | | | intron-variant | USP14 | GRCh38.p7 | 18:191485 | TTGATCAGTTTTGAC[-/A]AATGCAAATTCTCTG | 9097 |
rs777061466 | snp | A/G | 1.6516e-05 | 0.00287362 | intron-variant | USP14 | GRCh38.p7 | 18:198143 | ACTACGTATCCTTAT[A/G]AGCCAAGATATAGAC | 9097 |
rs777084143 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:197133 | TCCAGCTGCACAGGC[G/T]TCCTTAAACCTTTCA | 9097 |
rs777240336 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:209755 | ATTCAGGGTGTCTGT[C/T]ACTGTACTGTAACAA | 9097 |
rs777267975 | snp | A/G | 0.000300315 | 0.0122502 | intron-variant | USP14 | GRCh38.p7 | 18:158724 | ACTCCGGTGAGCCCT[A/G]TCCTGGCCTCGCGCG | 9097 |
rs777297190 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:162588 | TTTCTTCTTCTCTTA[A/G]ACTATCTAACCTTTC | 9097 |
rs777348857 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:164334 | ATGTAATTTTGTACA[C/T]GCATTTGTATGTTGA | 9097 |
rs777358887 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:189205 | TTCAAAGAATTGGCT[A/G]TTAGATTTGTTCATT | 9097 |
rs777388434 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:194412 | GTTCTTTACATTTTT[G/T]CTTCTTGATTTTTTA | 9097 |
rs777452207 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:169937 | CAGCCTCACCGACCC[A/G]CAGTTCCCTCCTCCC | 9097 |
rs777479881 | snp | G/T | 1.65277e-05 | 0.00287464 | missense | USP14 | GRCh38.p7 | 18:197681 | GGAAGCAATAGAGGA[G/T]GATTCTGTTAAAGAG | 9097 |
rs777548834 | in-del | -/C | | | intron-variant | USP14 | GRCh38.p7 | 18:199444 | ACGCATTTTGAGTTG[-/C]CCGATACACACAGTC | 9097 |
rs777593170 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:194330 | GTATCTTAGAATAAC[G/T]TAGAATTTCAGCAGC | 9097 |
rs777611026 | snp | A/C | 1.67307e-05 | 0.00289224 | intron-variant, synonymous-codon | USP14 | GRCh38.p7 | 18:178986 | TCCAGAAGAACCCTC[A/C]GCCAAAACTGTCTTC | 9097 |
rs777659595 | snp | A/G | 1.64895e-05 | 0.00287132 | synonymous-codon | USP14 | GRCh38.p7 | 18:210447 | AACACACCAGGGAAG[A/G]TCTAGTTCTTCAGGT | 9097 |
rs777734381 | snp | A/C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:179732 | AGCGAAAATTGTAGG[A/C/T]GTGCACCATCATGCC | 9097 |
rs777790491 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:183906 | TGAATAGGTAGTTTG[C/G]TGGGGTAGCTTTCTG | 9097 |
rs777900147 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:192918 | TTGTATACTAAATAT[A/G]CTACTTTTTGATAGG | 9097 |
rs777932201 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:165933 | GAGTAATATAGAATC[A/G]ACTTTATCCTATGAG | 9097 |
rs777946954 | snp | C/T | 8.28933e-05 | 0.00643737 | intron-variant | USP14 | GRCh38.p7 | 18:166851 | GAACGTTTATTATAA[C/T]GCAGTAACCTCATTA | 9097 |
rs777951371 | in-del | -/AAAG | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212202 | CTGCCTGTATTTTAA[-/AAAG]AAATACAAAGTTGTA | 9097 |
rs778023283 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:207569 | CTGTAGTCCCAGCTG[G/T]TCAGAAGGCTAAGGT | 9097 |
rs778054390 | snp | C/T | 0.000593697 | 0.0172191 | intron-variant | USP14 | GRCh38.p7 | 18:192824 | TTCTATTGTTTAACT[C/T]GGCTTTAATGTTCCT | 9097 |
rs778154388 | snp | A/G | | | missense | USP14 | GRCh38.p7 | 18:199251 | ACCAAAGGAAAGGAA[A/G]ATCAACTTCAGCTTA | 9097 |
rs778155845 | in-del | -/TATATAT | | | intron-variant | USP14 | GRCh38.p7 | 18:171026 | AAAAAAAAAAAAAAA[-/TATATAT]TATATATATATATAT | 9097 |
rs778170189 | snp | A/G | 1.66983e-05 | 0.00288944 | missense | USP14 | GRCh38.p7 | 18:209972 | TTTTTTCTCCTCAGA[A/G]TGACAAAAAGAGTAG | 9097 |
rs778289784 | in-del | -/CATG | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214012 | GATGATGATTGATTG[-/CATG]ATGATTGATAGTAAA | 9097 |
rs778365818 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:185556 | GGAGAGAACAGAAAA[G/T]CCCCATATCTCATCT | 9097 |
rs778440611 | snp | C/T | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:211693 | TTCAAACCACCATTC[C/T]GTAGCCACCCATCCT | 9097 |
rs778442111 | in-del | -/TC | | | intron-variant | USP14 | GRCh38.p7 | 18:162603 | ACTATCTAACCTTTC[-/TC]TCTCTCTCTCTTCTT | 9097 |
rs778449140 | snp | A/G | 3.39225e-05 | 0.00411826 | intron-variant | USP14 | GRCh38.p7 | 18:197567 | TTGGAAGAACTTTGT[A/G]GATCATTCACTGCCA | 9097 |
rs778466588 | snp | C/G | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212763 | GACCCTTGACTGATG[C/G]TAGGGAAAGGATAAA | 9097 |
rs778467116 | in-del | -/TT | | | intron-variant | USP14 | GRCh38.p7 | 18:180095 | AACTGTTTCTTTAGC[-/TT]GTGAAGGCAGAATAT | 9097 |
rs778467706 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:196882 | CTTCTCTAGTTCATG[C/T]CACGGCTGTCTCTTG | 9097 |
rs778496282 | snp | A/G | 4.95201e-05 | 0.0049757 | missense | USP14 | GRCh38.p7 | 18:210413 | ATAATTGTGGATACT[A/G]TGACTTACAAGCAGT | 9097 |
rs778509949 | snp | C/G | 1.65438e-05 | 0.00287605 | intron-variant | USP14 | GRCh38.p7 | 18:166831 | AAATGTAAGTATTAT[C/G]TTATGAACGTTTATT | 9097 |
rs778519874 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:164093 | TTGTATTACCAGATA[C/T]CTCTGTGGGTCAGGA | 9097 |
rs778547839 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:183984 | CAAGATTTCCTCTTT[A/G]CTGTTTTCTTCTTGG | 9097 |
rs778576909 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:162751 | CTTGGGAGTTTATTA[A/G]CCAATTTTATGACAT | 9097 |
rs778641613 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:190042 | TGTACAAATTGGGCC[C/T]ATTTGTCTGGCTGAT | 9097 |
rs778710356 | snp | A/T | 1.66192e-05 | 0.00288259 | | | GRCh38.p7 | 18:210021 | GTATGAACCCTTTTC[A/T]TTTGCTGATGGTAAG | 9097 |
rs778734356 | snp | C/G | 1.98576e-05 | 0.00315094 | | | GRCh38.p7 | 18:199356 | TGTTGTTTGTGAATT[C/G]CATGTTTGCGAGTAA | 9097 |
rs778770983 | snp | C/T | | | missense | USP14 | GRCh38.p7 | 18:204658 | CCAAATTCAAGGATC[C/T]AGAAGATAAAAAAGT | 9097 |
rs778829219 | snp | C/T | 1.66618e-05 | 0.00288628 | intron-variant | USP14 | GRCh38.p7 | 18:163475 | TGTAGTCCAAATTTT[C/T]ATCACATTACTATTA | 9097 |
rs778878812 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:172991 | ATCACATTTTTTAGT[C/G]ATTTGTACTATGTTG | 9097 |
rs778934007 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:172152 | CTGAGGCAGTAGGAT[C/T]GCTTAAGCCTAGGAG | 9097 |
rs778941121 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:205801 | AAAAATTATACAAAC[G/T]AAATAAAAACTCTTC | 9097 |
rs779022253 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:199872 | TCCCCTAGGAGCAGT[G/T]GTTCAGTATTCATTG | 9097 |
rs779049090 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:182478 | TTTAAAGGTTTTCTA[C/G]ATTTCTCTGAAGCGA | 9097 |
rs779073547 | snp | C/T | 2.2935e-05 | 0.00338629 | intron-variant | USP14 | GRCh38.p7 | 18:199152 | TTATATTCAAGAGTA[C/T]ATAACAAATTGAATA | 9097 |
rs779083484 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:165940 | ATAGAATCGACTTTA[-/T]CCTATGAGGGGAAAG | 9097 |
rs779109787 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:201146 | CCTAAACACAGTTGT[A/G]TGAAAAATAAATGCA | 9097 |
rs779133638 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:177709 | ATGCCTTCCAATTAA[C/G]ATACTGAGTAAGAGA | 9097 |
rs779136597 | in-del | -/TTT | | | intron-variant | USP14 | GRCh38.p7 | 18:174269 | TCACGTTTTTCTTTC[-/TTT]TTTTTTTTTTTTTTG | 9097 |
rs779138968 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:167436 | ATCCCTGAATATGAT[A/G]TACTTCCTTATTTAT | 9097 |
rs779154691 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:204538 | ATAAATGTGTTTACA[C/T]ATGTTTTTTGTTTGT | 9097 |
rs779170072 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:179948 | TTGCATATTTTGCCT[A/G]TTCTCTTCTCTTGAT | 9097 |
rs779259886 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:194132 | AGCCATCCAAGAGGT[A/G]TGAAGTGTTATCTCA | 9097 |
rs779271169 | in-del | -/AAGT | | | intron-variant | USP14 | GRCh38.p7 | 18:163865 | CCACTCTCCACCCTC[-/AAGT]AAGTTCCAGTGTCTT | 9097 |
rs779353821 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:174171 | TTGAGTCTTCTAACT[C/T]ACAAACATGGTAAAC | 9097 |
rs779385787 | snp | C/T | 1.64966e-05 | 0.00287194 | synonymous-codon | USP14 | GRCh38.p7 | 18:180316 | TATTCGTTCTGTGCC[C/T]GAACTCAAAGATGCC | 9097 |
rs779467119 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:156614 | ACATAATCTTATTTA[G/T]TCCTTATAACAATCC | 9097 |
rs779482021 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:166559 | GCTGGTTTCGAACTC[C/T]TGACCGCAGGTGATT | 9097 |
rs779504578 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:185178 | TATTTATTTATTTTC[A/G]AGACAGAGTCTCACT | 9097 |
rs779536185 | snp | A/G | 1.65132e-05 | 0.00287339 | intron-variant | USP14 | GRCh38.p7 | 18:192803 | TGAGTGTTAGAATGA[A/G]TTGAATTCTATTGTT | 9097 |
rs779541409 | snp | A/G | 3.34907e-05 | 0.00409197 | intron-variant | USP14 | GRCh38.p7 | 18:210367 | TGTCTAATATTAATG[A/G]ATTTACATCTTTCTT | 9097 |
rs779562533 | in-del | -/ATTTTATT | 1.65965e-05 | 0.00288062 | intron-variant | USP14 | GRCh38.p7 | 18:166855 | TTTATTATAATGCAG[-/ATTTTATT]TAACCTCATTATGAT | 9097 |
rs779577524 | snp | G/T | 1.66363e-05 | 0.00288407 | missense | USP14 | GRCh38.p7 | 18:209982 | TCAGAGTGACAAAAA[G/T]AGTAGTCCCCAGAAA | 9097 |
rs779609831 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:197600 | ATTACTTACTTTGTC[-/T]TTTTTTACATTACAG | 9097 |
rs779617168 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:198441 | GGGTTTCACCCTCTT[C/G]GTCAGGCTGGTATTG | 9097 |
rs779624108 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:202389 | AGCAGCTAAAGGCTT[C/T]CCCACATCTGTTAGG | 9097 |
rs779650528 | snp | A/G | 1.66971e-05 | 0.00288934 | intron-variant | USP14 | GRCh38.p7 | 18:196603 | ATTAAATATGTGACT[A/G]TTTTACTAAGGCAAT | 9097 |
rs779732476 | in-del | -/AA | | | intron-variant | USP14 | GRCh38.p7 | 18:163283 | TGTTATTTTTTAATT[-/AA]AAAAATTGTGATTTT | 9097 |
rs779799869 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:193036 | CATTATACTTAAGTT[A/G]AACAACTTGGTACTT | 9097 |
rs779835963 | snp | A/T | 1.6569e-05 | 0.00287824 | intron-variant | USP14 | GRCh38.p7 | 18:163463 | CTAAAGGTAAAATGT[A/T]GTCCAAATTTTCATC | 9097 |
rs779860286 | snp | A/G | 1.6656e-05 | 0.00288578 | missense | USP14 | GRCh38.p7 | 18:163353 | AAGGTGTAGAATTGA[A/G]TACAGATGAACCTCC | 9097 |
rs779862573 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:174449 | TTTTGTATTTTTAGT[A/G]GAGACGGGGTGTCAC | 9097 |
rs779913207 | snp | A/G | 1.64993e-05 | 0.00287218 | missense | USP14 | GRCh38.p7 | 18:198090 | CACCTTCTAAAAAGA[A/G]AAGTTTAATCGATCA | 9097 |
rs779996648 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:160983 | CCCAGTCTGGAGTGC[A/C]ATGGCGCGATGTTGG | 9097 |
rs780058344 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:205939 | GGTGTGAATTTACCA[C/T]AATCTGCTTCACCAT | 9097 |
rs780078029 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:173049 | ACAAGATTTTTTTTT[G/T]CTGTTTTCTTGTAAA | 9097 |
rs780123886 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:159811 | TGACCAGAGTTTCTT[C/T]TTTAAAATTTGAGCT | 9097 |
rs780129343 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:181940 | TTATTTTGCATGTGT[A/G]TATCCAGTTCTTCCA | 9097 |
rs780219201 | snp | A/G | 1.65192e-05 | 0.00287391 | intron-variant | USP14 | GRCh38.p7 | 18:192793 | TCTTCCCATTTGAGT[A/G]TTAGAATGAATTGAA | 9097 |
rs780244627 | in-del | -/TAGAT/TAGATAGAT | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:213966 | CTGTAATGGACAAGA[-/TAGAT/TAGATAGAT]TAGATAGATTAGATA | 9097 |
rs780323672 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:168372 | ATGACAATTTTACTT[C/T]TCCCTTTTCAATATT | 9097 |
rs780340576 | snp | A/G | 1.64917e-05 | 0.00287151 | missense | USP14 | GRCh38.p7 | 18:180300 | ATGCCACAGTTCAGT[A/G]TATTCGTTCTGTGCC | 9097 |
rs780392592 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:183638 | TCTACTTTGTTTCAC[C/T]GCTTACTTATCATGA | 9097 |
rs780466531 | snp | A/G | 1.83098e-05 | 0.00302565 | intron-variant | USP14 | GRCh38.p7 | 18:158718 | CGCTCTACTCCGGTG[A/G]GCCCTGTCCTGGCCT | 9097 |
rs780487629 | in-del | -/A | | | intron-variant | USP14 | GRCh38.p7 | 18:162888 | TGCAACCTTCGCCTC[-/A]CCGGGTTCAAGCGAT | 9097 |
rs780496732 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:164238 | TAGTAATTTTCTGTA[A/G]TGAGGTTGGAAAATT | 9097 |
rs780512857 | in-del | -/TAAAA | | | intron-variant | USP14 | GRCh38.p7 | 18:166710 | TGTTTTGAAGTACAT[-/TAAAA]TAAAATAAATTGATT | 9097 |
rs780516201 | snp | C/G | 1.65564e-05 | 0.00287714 | intron-variant | USP14 | GRCh38.p7 | 18:203062 | CTTGTATGGTATTTT[C/G]ATGTAATGGGATTTC | 9097 |
rs780569315 | in-del | -/T/TT/TTT | 0.55309 | 0.111861 | intron-variant | USP14 | GRCh38.p7 | 18:197741 | TTCGTTATACCTTGA[-/T/TT/TTT]TTTTTTTTTTTATTT | 9097 |
rs780643638 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:173210 | ACCTCCTGGTTCACG[C/T]CATTCTCCTGCCTCA | 9097 |
rs780673780 | snp | A/G | 9.68164e-05 | 0.00695692 | intron-variant | USP14 | GRCh38.p7 | 18:204523 | TAAATAAATATCTTT[A/G]TAAATGTGTTTACAC | 9097 |
rs780693975 | in-del | -/AAGTT | 1.65976e-05 | 0.00288072 | frameshift-variant | USP14 | GRCh38.p7 | 18:209999 | GTAGTCCCCAGAAAG[-/AAGTT]AAGTATGAACCCTTT | 9097 |
rs780758880 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:187802 | TAGTCCTTATATTCT[A/G]TGAAAATTTTAATGT | 9097 |
rs780762446 | in-del | -/TTTG | 1.65121e-05 | 0.00287329 | intron-variant | USP14 | GRCh38.p7 | 18:166767 | GGTGGTTAAATGTCT[-/TTTG]TTTGTCTTTGAAACA | 9097 |
rs780771886 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:190260 | TGAATATTCTAGTAC[A/C]TTTTTGGGCACATGC | 9097 |
rs780790196 | snp | A/G | 1.65067e-05 | 0.00287282 | missense | USP14 | GRCh38.p7 | 18:163445 | ATGGTGAAAGGAGGA[A/G]CGCTAAAGGTAAAAT | 9097 |
rs780795591 | snp | A/T | 1.65026e-05 | 0.00287246 | missense | USP14 | GRCh38.p7 | 18:204682 | AAAAAGTGAATCAGC[A/T]GCCAAATACAGTAGG | 9097 |
rs780811360 | snp | A/C | 3.3442e-05 | 0.004089 | missense | USP14 | GRCh38.p7 | 18:211279 | GAAGAGGAAAGTGAA[A/C]AGTAATCTTCATTTT | 9097 |
rs780829325 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:182749 | AACAGTTAGGTGTTA[C/T]CCCAGCCTGGATGAG | 9097 |
rs780885342 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:194010 | TGAGGAACTGCCAGA[A/G]TTTTCCAAAGGAGTC | 9097 |
rs780920742 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:207206 | TCATACCAGACTGAC[-/T]TGATTACTGTAGTTT | 9097 |
rs781032059 | in-del | -/G | | | intron-variant | USP14 | GRCh38.p7 | 18:174455 | ATTTTTAGTAGAGAC[-/G]GGGTGTCACCATGTT | 9097 |
rs781055095 | snp | A/G | 1.65176e-05 | 0.00287376 | missense | USP14 | GRCh38.p7 | 18:211183 | ATCGTAACACCAGAA[A/G]ATATCTTACGGCTTT | 9097 |
rs781066381 | snp | A/C | 1.68829e-05 | 0.00290537 | intron-variant, synonymous-codon | USP14 | GRCh38.p7 | 18:179004 | CAAAACTGTCTTCGT[A/C]GAAGACATGACAGAA | 9097 |
rs781082254 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:164403 | CTGGAAAACTGTTCA[-/T]TTTTTTTTTTTTGGC | 9097 |
rs781247488 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:193139 | AAATTATAATTTTGG[C/T]TTCAGGTTTGATTTG | 9097 |
rs781267554 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:160264 | AGCCAAGATCGCGCC[A/G]TTGCACTTCAGTCTG | 9097 |
rs781310982 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:156934 | ACATACAAAAAAAAT[C/T]AGCCGTGTGTGGTCC | 9097 |
rs781349773 | in-del | -/A | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213518 | GGAGAGGAGTAGGCC[-/A]AAAAAAAAAAAAGTC | 9097 |
rs781351149 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:205622 | CTACAAAATATGAAA[A/G]TAAAAAAAATCAGTT | 9097 |
rs781399378 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:176099 | ATTGGCAAATTATGA[G/T]TTGTCTGTTTCCTCT | 9097 |
rs781436554 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:190582 | GCCTACATAACTTTT[A/G]GTTTTTGGAAATTTG | 9097 |
rs781454964 | snp | C/T | 1.64925e-05 | 0.00287158 | synonymous-codon | USP14 | GRCh38.p7 | 18:180289 | TTGTTACATGAATGC[C/T]ACAGTTCAGTGTATT | 9097 |
rs781465097 | in-del | -/GAG | | | cds-indel | USP14 | GRCh38.p7 | 18:212553 | AAGTTGCAGTGAGCT[-/GAG]ATCACACCACTGCAC | 9097 |
rs781465193 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157920 | TTCAATTTATATATA[C/T]ATATATATAAATATA | 9097 |
rs781470355 | in-del | -/AGTT | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214110 | GAGCCATAGACAGTT[-/AGTT]AGTTAGTTAGTTATG | 9097 |
rs781504682 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:198723 | TTTTCATTCACCTTA[C/T]AAAGAATTAATTTCT | 9097 |
rs781520371 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:171787 | GGATTCACCTGAATT[A/C]TTGATACCATTAGGA | 9097 |
rs781571604 | in-del | -/TTAA | 1.68086e-05 | 0.00289896 | intron-variant | USP14 | GRCh38.p7 | 18:210050 | AGTAACATTCTCATT[-/TTAA]TTGAGTTATTGTATG | 9097 |
rs781626354 | in-del | -/ATT | | | intron-variant | USP14 | GRCh38.p7 | 18:161199 | TTCCAAAGTGCTGGG[-/ATT]ACAGGCATGAGCCAC | 9097 |
rs781714662 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:166959 | TACCTTTTCCCATTG[A/T]CTTGTGTTGGGCTCT | 9097 |
rs781752343 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:203939 | ATTGTAATCCCTTGA[-/T]TTAGGATCCAGCCTC | 9097 |
rs781772651 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:182408 | TGAAATGTTGTGATA[C/G]AACTGAGCAGAAGAG | 9097 |
rs781781535 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:177332 | GAGGCTGAGATGGGG[A/G]GATCACTTGAGGCCA | 9097 |
rs796071111 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:186224 | CCCAGTGCTTTGGGA[A/G]GCTGAATCTATAGCT | 9097 |
rs796229737 | in-del | -/TCTT | | | intron-variant | USP14 | GRCh38.p7 | 18:210779 | ATTTACATTTTTATG[-/TCTT]TCTGTTGTCTGGCTT | 9097 |
rs796256476 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:184424 | CCATCCTCACAAATA[C/T]TTAGCAGAACTTGTC | 9097 |
rs796274870 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:191511 | CTCTGTAATCCATTT[A/G]CCTATCAAAGTATAG | 9097 |
rs796313751 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:191255 | TTGTGAATTATTGTG[C/T]ATTGAAAAATTAAGA | 9097 |
rs796435610 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:156522 | CATACCCTGCAAAAT[C/G]CCTTTGAAGTTTTAC | 9097 |
rs796445306 | in-del | -/AT | | | intron-variant | USP14 | GRCh38.p7 | 18:196593 | AGTCGCGTGTATTAA[-/AT]ATGTGACTGTTTTAC | 9097 |
rs796480147 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:163046 | CTCCCAAAGTACTGG[A/G]ATTACAGGCGTGAGC | 9097 |
rs796522884 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:178618 | GCCTTGGCCTCAAAC[A/G]GCCACCCCAGTGCTT | 9097 |
rs796647154 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:191468 | TATCTTAAGTGTTTG[C/G]TTTGATCAGTTTTGA | 9097 |
rs796683212 | in-del | ATAAAAA/TT | | | intron-variant | USP14 | GRCh38.p7 | 18:204815 | TTTGTATAGTATTAT[ATAAAAA/TT]GGATCAATCTGTATT | 9097 |
rs796701058 | snp | C/T | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212689 | AAAATACCAAGCATA[C/T]GAGGTATTTCAATAT | 9097 |
rs796745137 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:179521 | GTCAACACGTGTCAA[-/T]TTTTTTTTTTAACAC | 9097 |
rs796747554 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:205333 | GTAAAACCTTACCTA[G/T]TGTTGACCTTGATGC | 9097 |
rs796757475 | in-del | -/TT | | | intron-variant | USP14 | GRCh38.p7 | 18:197742 | TTCGTTATACCTTGA[-/TT]TTTTTTTTTATTTTT | 9097 |
rs796783974 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:170646 | ATCAAACTAGCCACA[-/T]ACATTTTCTTAAGTC | 9097 |
rs796786437 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:204904 | TGTGTTTTATTTTCC[-/T]TTTTTTTTTTTTTGT | 9097 |
rs796818063 | multinucleotide-polymorphism | AT/GC | | | intron-variant | USP14 | GRCh38.p7 | 18:173401 | AGGCTTGAGCCACCA[AT/GC]CCCGGCCTATATTGT | 9097 |
rs796889037 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:188746 | GCAGTGGCATGATCT[C/T]GGCTCACTGCAACCT | 9097 |
rs796921795 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:208227 | TTCATATTGTGTTTG[C/T]TTTTGTAAATTGTTT | 9097 |
rs796968105 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:179573 | CATTCATTTTCATGG[-/T]TTTTTTTTTTTGCTT | 9097 |
rs797000789 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:169009 | ATGAGCCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 9097 |
rs797013308 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:164959 | ATTATTATTATTATT[A/T]TTTTTGGGATTGAGT | 9097 |