| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs770917288 | snp | C/T | | | upstream-variant-2KB | USP29 | GRCh38.p7 | 19:57119061 | GGACGCAGTTGCTAC[C/T]GCGCGGACCCGGCCC | 57663 |
| rs770983436 | snp | C/T | 1.65737e-05 | 0.00287864 | synonymous-codon | USP29 | GRCh38.p7 | 19:57129239 | TCTGAAGGAAGATAA[C/T]CCTGTACCAAACAAG | 57663 |
| rs771254506 | snp | C/T | 6.59131e-05 | 0.0057404 | missense | USP29 | GRCh38.p7 | 19:57130363 | GGAAATGTGAAGTCC[C/T]GGAAGTCTCTCAGGA | 57663 |
| rs771393093 | snp | A/G | 1.64909e-05 | 0.00287144 | missense | USP29 | GRCh38.p7 | 19:57129916 | AAATGCATGTTGGTA[A/G]TGCTGCCACCAAAGT | 57663 |
| rs771450216 | snp | C/T | 1.65201e-05 | 0.00287398 | synonymous-codon | USP29 | GRCh38.p7 | 19:57130931 | TCAGCAGGCACCACC[C/T]CCAGGTGTTAGGAAG | 57663 |
| rs771480773 | snp | G/T | 1.65463e-05 | 0.00287626 | missense | USP29 | GRCh38.p7 | 19:57129349 | GAGATTTGAAACTCG[G/T]GCCTTCATTCAATAC | 57663 |
| rs771514111 | in-del | -/ACTTCATCCTTGCAAAGAGAATCCTGT | 0.00145616 | 0.0269436 | cds-indel | USP29 | GRCh38.p7 | 19:57131462 | GACTCACTCGGCCTC[-/ACTTCATCCTTGCAAAGAGAATCCTGT]ACTTCATCCTTGCAA | 57663 |
| rs771581962 | snp | A/G | | | intron-variant | USP29 | GRCh38.p7 | 19:57123552 | AGAAAAGCAGTAAGC[A/G]GTGAAGCCGGGCTTG | 57663 |
| rs771763319 | snp | A/T | 3.54943e-05 | 0.00421259 | missense | USP29 | GRCh38.p7 | 19:57128682 | AAAGAAAGGATGATA[A/T]CTCTAAAGGTATGTG | 57663 |
| rs771767310 | snp | A/G | 3.29544e-05 | 0.00405908 | missense | USP29 | GRCh38.p7 | 19:57130008 | GCTTGTGGTCATGCT[A/G]TTCTCAAGGTAGAAC | 57663 |
| rs771770765 | in-del | -/ACG | 6.69288e-05 | 0.00578446 | cds-indel | USP29 | GRCh38.p7 | 19:57131413 | TCCCTCAGGGGGAAT[-/ACG]AAGGTGACTCTTTGT | 57663 |
| rs771772505 | snp | A/G | | | synonymous-codon | USP29 | GRCh38.p7 | 19:57129875 | GAATACTGGGAAAGA[A/G]TGTGGGGATGAAAAT | 57663 |
| rs771877746 | snp | A/G | 1.65296e-05 | 0.00287481 | missense | USP29 | GRCh38.p7 | 19:57129829 | GTTTAGACCAGCTGA[A/G]AGAAGACATGGAAAA | 57663 |
| rs771973122 | snp | C/G | 1.64985e-05 | 0.0028721 | missense | USP29 | GRCh38.p7 | 19:57130552 | ACCTGGAAAATGGCT[C/G]TGCACTAGAGTCAGA | 57663 |
| rs772113885 | snp | A/G | 4.94442e-05 | 0.00497188 | synonymous-codon | USP29 | GRCh38.p7 | 19:57130259 | GAAGAATAACGAGCA[A/G]GTTTATATTCCCAAA | 57663 |
| rs772141651 | snp | A/C | 1.65427e-05 | 0.00287595 | missense | USP29 | GRCh38.p7 | 19:57128842 | TTCAGCTGAGCAACA[A/C]CATTAGAAGTGTGGT | 57663 |
| rs772347168 | snp | A/G | | | intron-variant | USP29 | GRCh38.p7 | 19:57122151 | ATTGAAATAAAGTAA[A/G]ATAAGTCACTATCTA | 57663 |
| rs772376870 | snp | C/T | | | upstream-variant-2KB | USP29 | GRCh38.p7 | 19:57118639 | ATACTAAGTCACACA[C/T]CCACTGTGACAGCTC | 57663 |
| rs772414112 | snp | C/G | 3.30584e-05 | 0.00406548 | missense | USP29 | GRCh38.p7 | 19:57130956 | AGGAAGCTGGATGCC[C/G]AGGAACATACAGAAG | 57663 |
| rs772455276 | snp | A/G | 1.64912e-05 | 0.00287147 | synonymous-codon | USP29 | GRCh38.p7 | 19:57131189 | GAGCTCCCCAAATTC[A/G]GGCCATTACATCAGC | 57663 |
| rs772472464 | snp | A/C | 1.65321e-05 | 0.00287502 | missense | USP29 | GRCh38.p7 | 19:57129131 | TTTGTTTATGTCAAA[A/C]TCACCAACACATGTG | 57663 |
| rs772528512 | snp | A/T | | | intron-variant | USP29 | GRCh38.p7 | 19:57126081 | AAGAACGTTGAATAT[A/T]GGCCCCCACTGTCTT | 57663 |
| rs772719127 | in-del | -/A | | | downstream-variant-500B | USP29 | GRCh38.p7 | 19:57132152 | GGCGGACAGTGAGAG[-/A]AAAAAAGCATGGTCA | 57663 |
| rs772819268 | snp | A/G | | | upstream-variant-2KB | USP29 | GRCh38.p7 | 19:57119066 | CAGTTGCTACCGCGC[A/G]GACCCGGCCCCCGAC | 57663 |
| rs772836482 | snp | A/C | 1.64795e-05 | 0.00287045 | missense | USP29 | GRCh38.p7 | 19:57129525 | CATTCACAGCAACTG[A/C]AGCAGGGGTTCCCCA | 57663 |
| rs772991405 | in-del | -/A | | | frameshift-variant | USP29 | GRCh38.p7 | 19:57130527 | CAAGCCAAGAGCAGC[-/A]ATCAGAGAGACCTGG | 57663 |
| rs772992785 | snp | C/G | 0.000459015 | 0.0151426 | missense | USP29 | GRCh38.p7 | 19:57128685 | GAAAGGATGATATCT[C/G]TAAAGGTATGTGGAT | 57663 |
| rs773000243 | snp | C/T | 8.25008e-05 | 0.00642212 | synonymous-codon | USP29 | GRCh38.p7 | 19:57130557 | GAAAATGGCTCTGCA[C/T]TAGAGTCAGAATTGG | 57663 |
| rs773048511 | snp | A/G | | | upstream-variant-2KB | USP29 | GRCh38.p7 | 19:57120000 | ACTCTTCTGTTCCCA[A/G]GAGAATCAGGGGAGT | 57663 |
| rs773051974 | snp | A/G/T | 4.9473e-05 | 0.00497337 | missense | USP29 | GRCh38.p7 | 19:57129912 | CCACAAATGCATGTT[A/G/T]GTAGTGCTGCCACCA | 57663 |
| rs773067666 | snp | C/G | 1.65353e-05 | 0.00287531 | missense | USP29 | GRCh38.p7 | 19:57129368 | TTCATTCAATACCAA[C/G]TGTAATGGAAATCCT | 57663 |
| rs773347785 | snp | A/G | 1.64817e-05 | 0.00287064 | missense | USP29 | GRCh38.p7 | 19:57130260 | AAGAATAACGAGCAA[A/G]TTTATATTCCCAAAT | 57663 |
| rs773586897 | snp | A/G | 1.65187e-05 | 0.00287386 | missense | USP29 | GRCh38.p7 | 19:57130918 | TAGATGAATTTCTTC[A/G]GCAGGCACCACCTCC | 57663 |
| rs773621743 | snp | A/T | | | utr-variant-5-prime | USP29 | GRCh38.p7 | 19:57122438 | CATTTCTGAAAAAAG[A/T]ATTATCATCCACTCA | 57663 |
| rs773643563 | in-del | -/TT | 0.000328774 | 0.0128171 | frameshift-variant | USP29 | GRCh38.p7 | 19:57131426 | ATACGAAGGTGACTC[-/TT]TGTACAGACCTGCTT | 57663 |
| rs773770291 | in-del | -/TGGGAAAGAATGTGGGGATGAAAATTCATCTCCACAAA | 1.65002e-05 | 0.00287225 | frameshift-variant | USP29 | GRCh38.p7 | 19:57129866 | TGCCACTTTGAATAC[lengthTooLong]TGCATGTTGGTAGTG | 57663 |
| rs773860261 | in-del | -/T | 1.64781e-05 | 0.00287033 | frameshift-variant | USP29 | GRCh38.p7 | 19:57129584 | GTTTTACAATCGCTA[-/T]TTTGCAATTCCATCT | 57663 |
| rs773896187 | snp | A/C | | | intron-variant | USP29 | GRCh38.p7 | 19:57122128 | TAAATAAAAGTTTTT[A/C]ATTACCAATTGAAAT | 57663 |
| rs773998617 | snp | A/T | 1.65348e-05 | 0.00287526 | missense | USP29 | GRCh38.p7 | 19:57129813 | GAGTTTTTAGGTCAG[A/T]GTTTAGACCAGCTGA | 57663 |
| rs774002085 | snp | A/G | | | downstream-variant-500B | USP29 | GRCh38.p7 | 19:57132247 | TGCTTGAGCAGACCA[A/G]TTCAAAACCAGCCTG | 57663 |
| rs774038827 | in-del | -/GT | | | intron-variant | USP29 | GRCh38.p7 | 19:57122505 | GGTTTGCTTGTTTGG[-/GT]GATGGGATGTGTGTG | 57663 |
| rs774202742 | snp | A/G | 1.65477e-05 | 0.00287638 | missense | USP29 | GRCh38.p7 | 19:57130786 | CATTCGTAGAGTTCA[A/G]TTTTGACAGTGTCAC | 57663 |
| rs774246145 | snp | C/T | 1.65674e-05 | 0.00287809 | synonymous-codon | USP29 | GRCh38.p7 | 19:57129260 | ACCAAACAAGAAATA[C/T]AAGACAGATTCCTTG | 57663 |
| rs774382713 | snp | A/G | 0.000161159 | 0.00897516 | utr-variant-5-prime | USP29 | GRCh38.p7 | 19:57128675 | GTTACATAAAGAAAG[A/G]ATGATATCTCTAAAG | 57663 |
| rs774413378 | snp | A/T | 1.67055e-05 | 0.00289006 | missense | USP29 | GRCh38.p7 | 19:57131398 | CACAGGCAGGGGTGA[A/T]CCCTCAGGGGGAATA | 57663 |
| rs774452366 | snp | A/G | 1.64985e-05 | 0.0028721 | missense | USP29 | GRCh38.p7 | 19:57130156 | GTAAGCAGAAGAGTT[A/G]TGTTGCAAGGCATAC | 57663 |
| rs774501517 | snp | A/C | 3.3129e-05 | 0.00406982 | missense | USP29 | GRCh38.p7 | 19:57131074 | AAAACATTTTAGATG[A/C]AGAGAACACAAGAGG | 57663 |
| rs774820363 | snp | A/C | 1.65625e-05 | 0.00287766 | synonymous-codon | USP29 | GRCh38.p7 | 19:57129713 | CTGTAGTACAAAGAT[A/C]AAGAGAGAATTACTT | 57663 |
| rs774839345 | snp | A/G | 6.61004e-05 | 0.00574855 | synonymous-codon | USP29 | GRCh38.p7 | 19:57129095 | CAGCATTTGTAACAA[A/G]CCAAGTTATCAGAAG | 57663 |
| rs774849229 | snp | C/G | | | intron-variant | USP29 | GRCh38.p7 | 19:57125220 | GTTATAATTGGATTG[C/G]ACTGTGGTCTGAGAG | 57663 |
| rs774875326 | snp | G/T | 1.65176e-05 | 0.00287376 | stop-gained | USP29 | GRCh38.p7 | 19:57130671 | GTGATGTATGAAGAT[G/T]GAGGGAAGCTGATCA | 57663 |
| rs774888164 | snp | G/T | | | intron-variant | USP29 | GRCh38.p7 | 19:57127192 | TCTCCTGCATGAGGT[G/T]TCTCTCAACCCCTGT | 57663 |
| rs774892562 | snp | A/T | 1.65266e-05 | 0.00287455 | missense | USP29 | GRCh38.p7 | 19:57128977 | ATATGTTCCTGGACA[A/T]AATCCACCAAAACAA | 57663 |
| rs774913047 | snp | A/G | | | intron-variant | USP29 | GRCh38.p7 | 19:57123592 | AAGTTGGAATGTACA[A/G]TGTGTGATCTCGATG | 57663 |
| rs775014611 | snp | G/T | | | intron-variant | USP29 | GRCh38.p7 | 19:57124011 | TAAACCTCAGTTTCA[G/T]GACTCTGACCTTTTT | 57663 |
| rs775079188 | snp | C/T | 1.64779e-05 | 0.00287031 | stop-gained | USP29 | GRCh38.p7 | 19:57129576 | ATGAATGCAGTTTTA[C/T]AATCGCTATTTGCAA | 57663 |
| rs775144027 | snp | C/T | | | utr-variant-5-prime | USP29 | GRCh38.p7 | 19:57122352 | CTAATCCAGGCACTT[C/T]GGAAGGCTGAGGCTG | 57663 |
| rs775172023 | in-del | -/G | | | intron-variant | USP29 | GRCh38.p7 | 19:57124940 | CTTTCCTCCCATGAT[-/G]GAGCCTTAATTTTCT | 57663 |
| rs775376642 | snp | G/T | | | utr-variant-5-prime | USP29 | GRCh38.p7 | 19:57122331 | CTCCTCCAGGCGCTA[G/T]GGAGTCTAATCCAGG | 57663 |
| rs775387191 | snp | A/C | 1.64808e-05 | 0.00287057 | missense | USP29 | GRCh38.p7 | 19:57130276 | TTTATATTCCCAAAT[A/C]TTTAAGTTTATCTTC | 57663 |
| rs775605302 | snp | A/C/T | | | upstream-variant-2KB | USP29 | GRCh38.p7 | 19:57118742 | ATCTTCATGAATATT[A/C/T]CACCCCTTGGTTAAA | 57663 |
| rs775720073 | snp | C/G/T | 3.30815e-05 | 0.00406692 | synonymous-codon, missense | USP29 | GRCh38.p7 | 19:57128867 | TGTGGTCCTTAGACA[C/G/T]TGTAAAAAAAGACAA | 57663 |
| rs775900256 | snp | A/G | 1.65389e-05 | 0.00287562 | missense | USP29 | GRCh38.p7 | 19:57129361 | TCGGGCCTTCATTCA[A/G]TACCAACTGTAATGG | 57663 |
| rs776033869 | snp | A/G | 1.648e-05 | 0.0028705 | missense | USP29 | GRCh38.p7 | 19:57130054 | CCATCAACCTGCACC[A/G]AGAAACAAAACCACT | 57663 |
| rs776080625 | snp | C/G | 1.65021e-05 | 0.00287241 | missense | USP29 | GRCh38.p7 | 19:57130566 | TCTGCACTAGAGTCA[C/G]AATTGGTCCACTTTA | 57663 |
| rs776131979 | snp | A/G | 1.64972e-05 | 0.00287199 | synonymous-codon | USP29 | GRCh38.p7 | 19:57130484 | CAAGAATGCCGACCT[A/G]CAAAGATTCCAGAGA | 57663 |
| rs776312463 | snp | C/T | | | synonymous-codon | USP29 | GRCh38.p7 | 19:57130362 | GGGAAATGTGAAGTC[C/T]TGGAAGTCTCTCAGG | 57663 |
| rs776367083 | snp | C/T | | | intron-variant | USP29 | GRCh38.p7 | 19:57125014 | ATATGATGTCGACAA[C/T]TAATTTTGAGCTGTT | 57663 |
| rs776457224 | snp | A/C | | | synonymous-codon | USP29 | GRCh38.p7 | 19:57131162 | ACTCATCAGTGTTGT[A/C]AGCCATATCGGGAGC | 57663 |
| rs776502191 | snp | G/T | | | upstream-variant-2KB | USP29 | GRCh38.p7 | 19:57118804 | GGGCGTGATGCTCTG[G/T]GGTATGCCTGCACTT | 57663 |
| rs776535799 | snp | C/T | 0.000181412 | 0.00952224 | synonymous-codon | USP29 | GRCh38.p7 | 19:57131204 | AGGCCATTACATCAG[C/T]GATGTGTATGACTTT | 57663 |
| rs776546402 | snp | C/T | 1.65315e-05 | 0.00287498 | stop-gained | USP29 | GRCh38.p7 | 19:57129675 | ATTATGACCTTGACC[C/T]AGCTGCTTGCTTTGA | 57663 |
| rs776571282 | snp | G/T | | | intron-variant | USP29 | GRCh38.p7 | 19:57126139 | CACTATTAATCTGAT[G/T]GGCTTCCCTTTGTGG | 57663 |
| rs776599454 | snp | G/T | 1.64795e-05 | 0.00287045 | missense | USP29 | GRCh38.p7 | 19:57129545 | GGGGTTCCCCAATTT[G/T]GGAAACACCTGTTAC | 57663 |
| rs776811092 | in-del | -/C | 4.94784e-05 | 0.00497361 | frameshift-variant | USP29 | GRCh38.p7 | 19:57130203 | AGGGTCCTTATCATT[-/C]ATCTGAAACGCTATA | 57663 |
| rs777043013 | snp | A/G | | | downstream-variant-500B | USP29 | GRCh38.p7 | 19:57132357 | TTGGGAGGCCAAGGC[A/G]GGCGGATCACCTGAG | 57663 |
| rs777048841 | snp | A/G | 3.2956e-05 | 0.00405918 | missense | USP29 | GRCh38.p7 | 19:57130368 | TGTGAAGTCCTGGAA[A/G]TCTCTCAGGAGATGA | 57663 |
| rs777050782 | snp | A/T | 1.65367e-05 | 0.00287543 | missense | USP29 | GRCh38.p7 | 19:57129142 | CAAAATCACCAACAC[A/T]TGTGAAAAAGGGGAT | 57663 |
| rs777253166 | in-del | -/C | 7.30607e-05 | 0.00604359 | utr-variant-3-prime | USP29 | GRCh38.p7 | 19:57131463 | ACTCACTCGGCCTCA[-/C]TTCATCCTTGCAAAG | 57663 |
| rs777344243 | snp | C/G | 1.65682e-05 | 0.00287817 | synonymous-codon | USP29 | GRCh38.p7 | 19:57131030 | CCTGAATCACCTTGG[C/G]GCACTGGGTTCTGAC | 57663 |
| rs777481203 | snp | C/T | 1.65045e-05 | 0.00287263 | synonymous-codon | USP29 | GRCh38.p7 | 19:57131129 | CGTGAAGATGGGGGA[C/T]CCTCTCCAGGCCTAC | 57663 |
| rs777491144 | snp | C/T | | | intron-variant | USP29 | GRCh38.p7 | 19:57123395 | TATTCTTAGAATTAG[C/T]AATAGGAATATGATG | 57663 |
| rs777494963 | snp | C/T | 1.6516e-05 | 0.00287362 | missense | USP29 | GRCh38.p7 | 19:57130645 | TGGACCAGGGAGACA[C/T]TTCTCTTCCTGTGAT | 57663 |
| rs777563764 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon | USP29 | GRCh38.p7 | 19:57130013 | TGGTCATGCTGTTCT[C/T]AAGGTAGAACCTAAT | 57663 |
| rs777604447 | snp | C/T | | | intron-variant | USP29 | GRCh38.p7 | 19:57126394 | CACTTTCAGGTATAC[C/T]AATCAATCGTAGGTT | 57663 |
| rs777643176 | snp | C/G | | | upstream-variant-2KB | USP29 | GRCh38.p7 | 19:57118932 | GACACCAGTCAGGGT[C/G]GAGGCCTCACCAGCA | 57663 |
| rs777667069 | snp | A/G | 1.64789e-05 | 0.0028704 | missense | USP29 | GRCh38.p7 | 19:57130344 | AGCAGTAGTGCACCT[A/G]TTGGGAAATGTGAAG | 57663 |
| rs777849980 | snp | C/T | | | intron-variant | USP29 | GRCh38.p7 | 19:57121146 | GAAAATGCACTGCAA[C/T]AGAAAAATAAAAGTA | 57663 |
| rs777884660 | snp | A/G | 3.30431e-05 | 0.00406454 | synonymous-codon | USP29 | GRCh38.p7 | 19:57128933 | CTTGTTTATTGACAA[A/G]TTATCCTACAGAGAT | 57663 |
| rs777954108 | snp | G/T | 1.80305e-05 | 0.00300249 | utr-variant-3-prime | USP29 | GRCh38.p7 | 19:57131454 | GCTTGACAGACTCAC[G/T]CGGCCTCACTTCATC | 57663 |
| rs778007374 | snp | A/G | 1.66549e-05 | 0.00288568 | missense | USP29 | GRCh38.p7 | 19:57131388 | CTACCTAGCACACAG[A/G]CAGGGGTGATCCCTC | 57663 |
| rs778009612 | snp | G/T | 1.64993e-05 | 0.00287218 | missense | USP29 | GRCh38.p7 | 19:57129867 | GCCACTTTGAATACT[G/T]GGAAAGAATGTGGGG | 57663 |
| rs778338811 | snp | C/T | 3.31016e-05 | 0.00406813 | missense | USP29 | GRCh38.p7 | 19:57129345 | GATAGAGATTTGAAA[C/T]TCGGGCCTTCATTCA | 57663 |
| rs778466117 | snp | C/T | 1.64876e-05 | 0.00287116 | missense | USP29 | GRCh38.p7 | 19:57130426 | CATCAATGAAGCTGA[C/T]CTCAGAATCCAGTGA | 57663 |
| rs778519114 | snp | C/T | 1.65531e-05 | 0.00287686 | synonymous-codon | USP29 | GRCh38.p7 | 19:57131003 | TACAGAATTAAGACT[C/T]CAAAAGGCTGACCTG | 57663 |
| rs778521345 | snp | C/G | 1.64925e-05 | 0.00287158 | missense | USP29 | GRCh38.p7 | 19:57129905 | TTCATCTCCACAAAT[C/G]CATGTTGGTAGTGCT | 57663 |
| rs778553568 | in-del | -/T | 0.000198636 | 0.00996386 | frameshift-variant | USP29 | GRCh38.p7 | 19:57131335 | ACATGCACAATGGGA[-/T]TTTTGAGGAGCTGTT | 57663 |
| rs778568907 | snp | C/T | 1.65594e-05 | 0.0028774 | missense | USP29 | GRCh38.p7 | 19:57129313 | AGAACCCATCAAGTT[C/T]AGAGGATTTAGAAAA | 57663 |
| rs778574223 | snp | C/G | 1.65247e-05 | 0.00287438 | missense | USP29 | GRCh38.p7 | 19:57130892 | CCAGCAGTGTATTGA[C/G]GAGAGCATCATAGAT | 57663 |
| rs778585733 | snp | C/G | 7.4438e-05 | 0.00610028 | utr-variant-3-prime | USP29 | GRCh38.p7 | 19:57131478 | CTTCATCCTTGCAAA[C/G]AGAATCCTGTACTTC | 57663 |
| rs778704814 | snp | C/T | 3.30611e-05 | 0.00406565 | synonymous-codon | USP29 | GRCh38.p7 | 19:57128912 | AACTTTGAAAAACAA[C/T]GTGTTCTTGTTTATT | 57663 |
| rs778706139 | snp | C/T | 1.65501e-05 | 0.00287659 | missense | USP29 | GRCh38.p7 | 19:57128824 | GAAAATTTATAAGAA[C/T]TTTTCAGCTGAGCAA | 57663 |
| rs778794837 | snp | A/G | | | intron-variant | USP29 | GRCh38.p7 | 19:57121759 | TAAAACAAAAAGCAC[A/G]GTTACTACAAAGAAA | 57663 |
| rs778850666 | snp | A/G | | | intron-variant | USP29 | GRCh38.p7 | 19:57123525 | GGAGGGTTGAGTTTC[A/G]GCCTTAGTGTTAGAA | 57663 |
| rs779038356 | snp | A/G | 1.64795e-05 | 0.00287045 | missense | USP29 | GRCh38.p7 | 19:57129984 | TTGCAGCTCTCCCTT[A/G]TTTGTAAAGCTTGTG | 57663 |
| rs779088749 | snp | C/T | 1.64846e-05 | 0.0028709 | missense | USP29 | GRCh38.p7 | 19:57130413 | AGCCCATTGACACCA[C/T]CAATGAAGCTGACCT | 57663 |
| rs779147687 | snp | C/G | 1.65425e-05 | 0.00287593 | missense | USP29 | GRCh38.p7 | 19:57130749 | CAACATCCAGAACTT[C/G]AGAAGTATGAGAAAA | 57663 |
| rs779192938 | snp | G/T | 1.65658e-05 | 0.00287795 | missense | USP29 | GRCh38.p7 | 19:57129203 | CACACTATCATCTGA[G/T]GTACAGACAAATGAG | 57663 |
| rs779237293 | snp | A/C | 8.25866e-05 | 0.00642546 | missense | USP29 | GRCh38.p7 | 19:57129667 | AGGCTCTTATTATGA[A/C]CTTGACCCAGCTGCT | 57663 |
| rs779367461 | in-del | -/A | 4.97137e-05 | 0.00498542 | frameshift-variant | USP29 | GRCh38.p7 | 19:57129737 | TTACTTGGGAATGTT[-/A]AAAAAAGTCATTTCA | 57663 |
| rs779473486 | snp | C/T | 1.64792e-05 | 0.00287042 | synonymous-codon | USP29 | GRCh38.p7 | 19:57130334 | TCTTCCCTTGAGCAG[C/T]AGTGCACCTGTTGGG | 57663 |
| rs779494965 | in-del | -/CT | 1.64781e-05 | 0.00287033 | frameshift-variant | USP29 | GRCh38.p7 | 19:57129506 | CCAGGTGCCTCTTGA[-/CT]CTCATTCACAGCAAC | 57663 |
| rs779522609 | snp | G/T | 1.66219e-05 | 0.00288283 | synonymous-codon | USP29 | GRCh38.p7 | 19:57131372 | AGCAGAGAACTCTCG[G/T]CTACCTAGCACACAG | 57663 |
| rs779571653 | snp | C/T | 1.65455e-05 | 0.00287619 | synonymous-codon | USP29 | GRCh38.p7 | 19:57130769 | GTATGAGAAAACCAA[C/T]ACATTCGTAGAGTTC | 57663 |
| rs779597227 | snp | A/C | | | intron-variant | USP29 | GRCh38.p7 | 19:57124664 | TAGGTGCCTGCCACC[A/C]TGCCCGGCTAATTTT | 57663 |
| rs779608956 | snp | C/T | 1.65225e-05 | 0.00287419 | synonymous-codon | USP29 | GRCh38.p7 | 19:57129062 | TATGCTGAAGGAAAT[C/T]GACAAAACTTCATTT | 57663 |
| rs779747746 | snp | A/G | 1.65644e-05 | 0.00287783 | synonymous-codon | USP29 | GRCh38.p7 | 19:57129194 | GGGGCAAAACACACT[A/G]TCATCTGATGTACAG | 57663 |
| rs779837668 | snp | C/G | 1.64833e-05 | 0.00287078 | missense | USP29 | GRCh38.p7 | 19:57129962 | TGTTGCTAATTTTGA[C/G]TTTGAATTGCAGCTC | 57663 |
| rs779992025 | in-del | -/G | 3.29807e-05 | 0.0040607 | frameshift-variant | USP29 | GRCh38.p7 | 19:57131171 | GTTGTCAGCCATATC[-/G]GGGAGCTCCCCAAAT | 57663 |
| rs780064840 | snp | C/T | | | intron-variant | USP29 | GRCh38.p7 | 19:57120327 | AACAAAGTGAGACTA[C/T]GTCTCAAAAAAATTT | 57663 |
| rs780122728 | snp | A/T | | | upstream-variant-2KB | USP29 | GRCh38.p7 | 19:57119706 | GGGATGACAGGCGTG[A/T]GCCACCGCGCCCGGC | 57663 |
| rs780137813 | snp | A/G | 3.30246e-05 | 0.0040634 | synonymous-codon | USP29 | GRCh38.p7 | 19:57130616 | AAAGGAGCTTCCAGT[A/G]GCTGACTCACTGATG | 57663 |
| rs780370092 | snp | C/T | 3.29973e-05 | 0.00406172 | synonymous-codon | USP29 | GRCh38.p7 | 19:57130529 | AAGCCAAGAGCAGCA[C/T]CAGAGAGACCTGGAA | 57663 |
| rs780401096 | snp | C/T | 1.64999e-05 | 0.00287222 | missense | USP29 | GRCh38.p7 | 19:57131281 | TCTCAGAGACCAAAA[C/T]GCAGGAGGCGAGGCT | 57663 |
| rs780527601 | snp | C/G | | | intron-variant | USP29 | GRCh38.p7 | 19:57127741 | GGACCTGCTGAGTGA[C/G]ATCACTTGGCCCCCT | 57663 |
| rs780595584 | snp | C/T | 1.64904e-05 | 0.00287139 | synonymous-codon | USP29 | GRCh38.p7 | 19:57131168 | CAGTGTTGTCAGCCA[C/T]ATCGGGAGCTCCCCA | 57663 |
| rs780693213 | snp | C/T | 1.6525e-05 | 0.00287441 | missense | USP29 | GRCh38.p7 | 19:57129052 | AAAGCAGGAATATGC[C/T]GAAGGAAATTGACAA | 57663 |
| rs780702815 | snp | A/G | 3.30442e-05 | 0.0040646 | missense | USP29 | GRCh38.p7 | 19:57128949 | TTATCCTACAGAGAT[A/G]CTAAACAGTTGAATA | 57663 |
| rs780756096 | snp | A/T | 0.00016497 | 0.00908063 | stop-gained | USP29 | GRCh38.p7 | 19:57130127 | AGAAGAGCTTGAATA[A/T]AACTGTCAGATGTGT | 57663 |
| rs780851981 | snp | A/G | 3.30868e-05 | 0.00406723 | missense | USP29 | GRCh38.p7 | 19:57130758 | GAACTTCAGAAGTAT[A/G]AGAAAACCAATACAT | 57663 |
| rs780916266 | snp | C/T | 1.65351e-05 | 0.00287528 | missense | USP29 | GRCh38.p7 | 19:57129795 | ATGCAGAATGATGCT[C/T]ATGAGTTTTTAGGTC | 57663 |
| rs781036255 | snp | C/T | | | downstream-variant-500B | USP29 | GRCh38.p7 | 19:57132029 | AGTGCCCAAAACCAT[C/T]CTGAGATCGGGCCGG | 57663 |
| rs781111960 | in-del | -/A | 1.65403e-05 | 0.00287574 | frameshift-variant | USP29 | GRCh38.p7 | 19:57129147 | TCACCAACACATGTG[-/A]AAAAGGGGATATTAG | 57663 |
| rs781241321 | snp | A/G | 4.95528e-05 | 0.00497734 | missense | USP29 | GRCh38.p7 | 19:57130661 | TTCTCTTCCTGTGAT[A/G]TATGAAGATGGAGGG | 57663 |
| rs781268343 | snp | A/T | | | intron-variant | USP29 | GRCh38.p7 | 19:57125512 | TGATCCCTTTACCAT[A/T]ATGTAATGCCCTCTT | 57663 |
| rs781368378 | snp | A/G/T | 3.29958e-05 | 0.00406165 | missense, stop-gained | USP29 | GRCh38.p7 | 19:57130521 | GGAGATGCAAGCCAA[A/G/T]AGCAGCATCAGAGAG | 57663 |
| rs781370761 | snp | A/G | 3.30885e-05 | 0.00406733 | synonymous-codon | USP29 | GRCh38.p7 | 19:57129350 | AGATTTGAAACTCGG[A/G]CCTTCATTCAATACC | 57663 |
| rs781420517 | snp | G/T | 1.65512e-05 | 0.00287669 | missense | USP29 | GRCh38.p7 | 19:57128815 | TCAAATCTGGAAAAT[G/T]TATAAGAATTTTTCA | 57663 |
| rs781425923 | snp | C/T | 1.64895e-05 | 0.00287132 | missense | USP29 | GRCh38.p7 | 19:57130434 | AAGCTGACCTCAGAA[C/T]CCAGTGATTCCCTGG | 57663 |
| rs781530617 | snp | A/G | 1.84198e-05 | 0.00303472 | utr-variant-3-prime | USP29 | GRCh38.p7 | 19:57131467 | ACTCGGCCTCACTTC[A/G]TCCTTGCAAAGAGAA | 57663 |
| rs781773811 | snp | C/T | 1.64784e-05 | 0.00287035 | missense | USP29 | GRCh38.p7 | 19:57129475 | ACAGCCAGGGTGACC[C/T]AAGATGCAACAAAGC | 57663 |
| rs796165921 | snp | C/T | | | intron-variant | USP29 | GRCh38.p7 | 19:57127698 | TTTCAAGCCAGTGGT[C/T]CTTAGCTTGCTGGGC | 57663 |
| rs796322403 | snp | A/G | | | intron-variant | USP29 | GRCh38.p7 | 19:57122557 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGAGTGT | 57663 |
| rs796421807 | in-del | -/TT | | | intron-variant | USP29 | GRCh38.p7 | 19:57124476 | TGTGGGGTTTTTTTT[-/TT]GGTTTTCTTTTTTGT | 57663 |
| rs796456210 | snp | A/C | | | intron-variant | USP29 | GRCh38.p7 | 19:57120696 | GGAGGCTGAGGCAGG[A/C]GAATCACTTGAACCC | 57663 |
| rs796540485 | multinucleotide-polymorphism | CA/TG | | | intron-variant | USP29 | GRCh38.p7 | 19:57125933 | TTTAGTGCTTCCTCC[CA/TG]GAGCTCTTGTAAGGT | 57663 |
| rs796590283 | snp | A/G | | | intron-variant | USP29 | GRCh38.p7 | 19:57120789 | GAGAGACTCCGTCTC[A/G]AAAAAAAAAAAAAAA | 57663 |