| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs190827574 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109057867 | TCTGGGTCCCACATG[G/T]GAGAGAAATTGATCA | 84749 |
| rs190837454 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP30 | GRCh38.p7 | 12:109035418 | TGCCAGGCTGGAGTG[C/T]AGTGGCACAATCTCG | 84749 |
| rs190904968 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109051033 | CAATAATTTTCACAT[A/G]GAAATGACATATTTT | 84749 |
| rs191033174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109073209 | TTTTAAAATGTGGCT[C/T]TACCCATTATACAGA | 84749 |
| rs191047961 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109034981 | GATACCACTTTTTCC[A/G]TCCATTTACTTTTAA | 84749 |
| rs191087554 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109078924 | ACATTGTTCTATTGT[C/T]TTCTGGCCTCCATTT | 84749 |
| rs191264682 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109079632 | CAGCCTCCCAAAGTG[C/T]TGGGATTACAGGTGT | 84749 |
| rs191268913 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109063395 | CGTGAGCCACCACGC[A/C]AGGCCTAGGCTGAAT | 84749 |
| rs191273036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109041505 | CCAGGCATGGTGGTG[C/T]GTGCCTGTTGTCCCA | 84749 |
| rs191283358 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022416 | GGAACAAGAAAACCA[A/G]TCTGAGAACTGAAAA | 84749 |
| rs191291168 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109078272 | CTACTAAAATTACAA[A/C]AATTAGCTGGGCCTG | 84749 |
| rs191346476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109062672 | TATAGTTTGTCTTCT[A/G]TGAATTGCTAGTTTA | 84749 |
| rs191372939 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | USP30 | GRCh38.p7 | 12:109029400 | GCTTGGAATGTTTCT[G/T]TGTCTCTGTCTTGCT | 84749 |
| rs191424833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109067803 | ATCAGAGGGGAGATA[C/T]AGCTGTTTTTCACTC | 84749 |
| rs191426781 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109087335 | GGGGGTGAGCTGGCA[C/G]ACACACCAAACAGTG | 84749 |
| rs191440246 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109047565 | ACATTATACATGTTC[A/G]TGTGAAAGCATCTTG | 84749 |
| rs191443928 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109065576 | TACTGAACAGAATTA[C/T]AACATTTTCCATACA | 84749 |
| rs191584193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109062430 | AGCTCCACCTCCTGG[A/G]TTCAAGCTAGTCTCC | 84749 |
| rs191686240 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109083542 | GGTCTCATTTAAGCC[A/G]GGTAGCTATTATCGC | 84749 |
| rs191688291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109058591 | AAAAAAAAAAAATCA[A/G]AGATGGAACCATTTA | 84749 |
| rs191760833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109064517 | AACTCCTGACCTGAA[A/G]TGATTAACCACCTCG | 84749 |
| rs191776641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109043463 | TTGACAAGAGTACCA[A/G]TACGATTGAATGGGA | 84749 |
| rs191782871 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109070892 | AGCAACCCAAGTGTT[C/T]ATCGGCTGATAAATA | 84749 |
| rs191884814 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109039897 | TACAGGCGTGAACCA[C/T]CACACCTGGCCAGCC | 84749 |
| rs191895354 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109085199 | TAAGGTGAAGTTTCA[C/T]GATTACACATTCCTA | 84749 |
| rs191906714 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109067201 | TCACTGCAAGCTCCG[C/T]CTCCCGGGTTCATGC | 84749 |
| rs191913556 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046928 | TCTCGAACTCCTGAC[C/T]TCAGGTGATCCACCC | 84749 |
| rs191924741 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109027506 | GCTGGTCTCGAACTC[C/T]GGCTTCAAGCAATCC | 84749 |
| rs192077519 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109078381 | GTGAGCCGAGATCAC[A/G]CCACTGCACTTCAGT | 84749 |
| rs192149982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109071414 | CTCTCCTGCTCTCTG[C/T]TCCTGGACCTCTTGC | 84749 |
| rs192166108 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | USP30 | GRCh38.p7 | 12:109030988 | ATATACAGTATTTTT[A/T]AAATCAGGGGATGCT | 84749 |
| rs192280818 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109051149 | CTCACCTGGCCTCCC[A/G]AAGTGCTGGGATTAT | 84749 |
| rs192289156 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109030026 | TCATTATTGAAATAC[A/G]TGTTGAACTATATTT | 84749 |
| rs192440885 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109036814 | GTCTTATTAAGTATA[C/T]CTTTTATGTGAGGGT | 84749 |
| rs192491246 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109028357 | GTACAGGAAGCATGG[A/C/T]GCTGGCATCTGCTTC | 84749 |
| rs192494353 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109059030 | CATGTCTGGGAGTCC[C/G]CCTTATGAAAATGGT | 84749 |
| rs192537481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053409 | GGTCCTGTTAAAGCC[C/T]TCCGTTCTTGTTAGG | 84749 |
| rs192584701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109074805 | TATTAACTGTAGTCA[C/T]CATGCTGTACGTTAA | 84749 |
| rs192588414 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | USP30 | GRCh38.p7 | 12:109059335 | GAGTAGCTGGGATGA[C/G]AGGTCTGTGCCACCA | 84749 |
| rs192627640 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB, nc-transcript-variant | USP30, USP30-AS1 | GRCh38.p7 | 12:109052495 | GGACGTGGTCCGTCA[A/G]CTATTGCTCTCCGGG | 84749 |
| rs192741079 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP30 | GRCh38.p7 | 12:109081611 | TTTTTGAATACACAC[A/G]CACGCATGCGCGCAC | 84749 |
| rs192798969 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109074446 | ACCTTTTAAGGAACT[C/G]CCAGACTGTTTTCCA | 84749 |
| rs192807115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109036553 | TCCACCCTGCTTGGC[C/T]TCCCAAAGTGCTGGG | 84749 |
| rs192981875 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109063781 | TCCCTAATGATAAGT[C/T]ATATTGAGCATCTTT | 84749 |
| rs192990285 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109023703 | CAATGGCGCAATCTC[A/G/T]GCTCACTGCTACCTC | 84749 |
| rs193058854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046056 | CTGCAAGCAGAATTC[C/T]CTCTTATTCTTCCCT | 84749 |
| rs193123175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109084714 | GGAAGCTCAAAGATC[C/T]CAGGCTAGCCGTAAA | 84749 |
| rs193193028 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109080683 | ACAGTCATGTGCTAT[A/T]TAATGATGTTTTGGT | 84749 |
| rs193197512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109042236 | ATGTCAATTTTGATG[C/T]TGTGTTTCCATTATG | 84749 |
| rs193231210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109066795 | AATACAAGCAAAGGC[C/T]TTGGGAAACAGCCCT | 84749 |
| rs193235435 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109027082 | TTGGGGTGGACACAA[A/G]CATTCAGTCCTTAAC | 84749 |
| rs199642467 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | USP30 | GRCh38.p7 | 12:109079351 | TTTCTTTTTTTTTTT[C/T]TTTTTTTTTTTTTTT | 84749 |
| rs199671452 | snp | A/G | 5.00973e-05 | 0.00500461 | missense | USP30 | GRCh38.p7 | 12:109085881 | CTGTTCTACGAGCGC[A/G]TCCTTTCCAGGATGC | 84749 |
| rs199763379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109066553 | GTCGGGCATGGTAGC[A/G]CATGCCTTGTAATCC | 84749 |
| rs199950869 | snp | C/T | 9.90917e-05 | 0.00703818 | intron-variant | USP30 | GRCh38.p7 | 12:109072296 | GTTTTTTTTTTTTCT[C/T]CCCTACAGCAGCAGT | 84749 |
| rs200040409 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109085968 | GAGCTGATGGCACTG[C/T]CTGCACTGTCCAGGA | 84749 |
| rs200043270 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109024625 | ACTGGTAAAGCAGCA[-/T]TTTTTTTTTCCCGAG | 84749 |
| rs200167889 | snp | A/G | 0.000198259 | 0.0099544 | synonymous-codon, intron-variant | USP30 | GRCh38.p7 | 12:109056769 | TTGGGGTCCCATTAC[A/G]GAAAGAAAGAAGCGT | 84749 |
| rs200296692 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109041325 | TTCCTGAAAGCTTGC[C/T]GGGGCTTCATGATTT | 84749 |
| rs200338946 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109075842 | TCATGTTACTTTTTC[C/T]TTTTTTTTTTTTTTT | 84749 |
| rs200368521 | in-del | -/T | 0.0123036 | 0.0774623 | intron-variant | USP30 | GRCh38.p7 | 12:109077965 | GCCTTTGTGCTATTA[-/T]TACATACATTATAAA | 84749 |
| rs200384603 | in-del | -/TTTC | | | intron-variant | USP30 | GRCh38.p7 | 12:109036296 | ATGTTCCTTTTAGTA[-/TTTC]TTTCTTTCTTTTTTT | 84749 |
| rs200396077 | in-del | -/G | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046504 | CTATTTTACTCAAAA[-/G]TCCACCAATTTAAAT | 84749 |
| rs200411618 | in-del | -/A | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055400 | TATATATATATATAT[-/A]TTTTTTTTTTTTTTT | 84749 |
| rs200428194 | snp | A/T | 1.67192e-05 | 0.00289125 | intron-variant | USP30 | GRCh38.p7 | 12:109082768 | CACTACACACCCTGT[A/T]GGCTTTGTTTTGAGG | 84749 |
| rs200429871 | snp | A/C | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | USP30, USP30-AS1 | GRCh38.p7 | 12:109054529 | AGCAAGACACTGTCT[A/C]AAAAAAAAATAAAAA | 84749 |
| rs200435024 | snp | A/G | 1.6473e-05 | 0.00286988 | missense | USP30 | GRCh38.p7 | 12:109085750 | TTGTCACTTACCGAC[A/G]GTCCCCACCTTCTGC | 84749 |
| rs200472021 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon | USP30 | GRCh38.p7 | 12:109085709 | GGCAGTTGTCGTCCA[C/T]CATGGAGACATGCAC | 84749 |
| rs200522064 | in-del | -/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109038206 | GTATGTTGGTTCCCG[-/C]CCCCCTCCCCACCTG | 84749 |
| rs200619378 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109058571 | GAGCGAAACTCCGTC[C/T]CAAAAAAAAAAAAAA | 84749 |
| rs200633278 | snp | C/T | 9.91309e-05 | 0.00703958 | missense | USP30 | GRCh38.p7 | 12:109085025 | CATCTTTATTGCCAA[C/T]GCTGTCAGCGCCGAT | 84749 |
| rs200652176 | snp | C/T | 0.00018185 | 0.00953372 | missense | USP30 | GRCh38.p7 | 12:109072341 | AAACAAATTACCTGC[C/T]GCACAAGAGGTAGCT | 84749 |
| rs200654716 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109076425 | CTTTTTTTTTTTTTT[A/G]TTTGCCTTATTATCC | 84749 |
| rs200689726 | snp | A/C | 1.6495e-05 | 0.0028718 | missense, intron-variant | USP30 | GRCh38.p7 | 12:109056743 | GCTCTTGCAGCAGGA[A/C]TATATGTTATTTGGG | 84749 |
| rs200769239 | snp | A/G | 0.000167065 | 0.00913808 | intron-variant | USP30 | GRCh38.p7 | 12:109056650 | TTTTGTGTTTGTGTG[A/G]GGGAAGACAGTAAAC | 84749 |
| rs200783368 | snp | C/T | 3.43672e-05 | 0.00414517 | intron-variant | USP30 | GRCh38.p7 | 12:109084912 | TTTTGTTTACAGAGC[C/T]ACTGCTAATTTTCAT | 84749 |
| rs200785531 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109056202 | GTTGTTGTTGTTGTT[G/T]TTTTTTATGAGACTG | 84749 |
| rs200794833 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109037619 | TTTTGTGGCTTTTCT[A/C]AACTAATTCCATAAA | 84749 |
| rs200893038 | in-del | -/TTTCT | | | intron-variant | USP30 | GRCh38.p7 | 12:109036304 | TTTAGTATTTCTTTC[-/TTTCT]TTTTTTTTTTTTTAG | 84749 |
| rs200972983 | in-del | -/TATATATTTTTT | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055395 | ATATATATATATATA[-/TATATATTTTTT]TTTTTTTTTTTTTTG | 84749 |
| rs200975633 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109036307 | AGTATTTCTTTCTTT[C/T]TTTTTTTTTTTTTTA | 84749 |
| rs201090244 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109058715 | CAAAAACATTAAAGT[-/A]AAAAAAAAATGTCCG | 84749 |
| rs201279666 | snp | C/T | 0.00016536 | 0.00909136 | missense | USP30 | GRCh38.p7 | 12:109085049 | CGCCGATGCCCTTCC[C/T]TCTCCCAGTTGTTCC | 84749 |
| rs201327948 | snp | C/T | 0.00199802 | 0.0315439 | intron-variant | USP30 | GRCh38.p7 | 12:109085089 | GTGAGCCACCCTTTA[C/T]AAGCCCCATCTTAGA | 84749 |
| rs201356936 | in-del | -/A | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055829 | TAAAAAAAAAAAAAA[-/A]GAAAAGAAAAAAAAC | 84749 |
| rs201467206 | snp | A/G | 5.06052e-05 | 0.00502991 | intron-variant | USP30 | GRCh38.p7 | 12:109085108 | CCCCATCTTAGAGCT[A/G]CCACTGCTCTTAGCT | 84749 |
| rs201519201 | snp | A/C/T | 0.00188832 | 0.0306695 | intron-variant, synonymous-codon, stop-gained | USP30 | GRCh38.p7 | 12:109083074 | CCAGGTGTGTGCGCG[A/C/T]GAGGAGCCGATGCAG | 84749 |
| rs201561858 | snp | C/T | 0.00460675 | 0.0477719 | intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088516 | CCATCTTTATACCTG[C/T]AATGAGAAAACAAAC | 84749 |
| rs201563320 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109061409 | AAAAAAAAAAAAAAA[A/T]ATTTTTTTTTTTTTT | 84749 |
| rs201623307 | snp | C/T | 0.000510645 | 0.0159707 | missense | USP30 | GRCh38.p7 | 12:109081383 | CACTAAGTATTCCAG[C/T]CGCCACATGGGTATG | 84749 |
| rs201650122 | snp | A/C | 0.000399281 | 0.0141238 | synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088260 | CACCCGTGGAGCCAG[A/C]ACCTTCTTTCTCACG | 84749 |
| rs201661228 | in-del | -/A | | | intron-variant | USP30 | GRCh38.p7 | 12:109040176 | CTACATATGGCAAAC[-/A]AAAAAAAAATTTAGG | 84749 |
| rs201680743 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109031941 | GACCTCATCGCTACA[-/T]TTTTTTTTTAATTAG | 84749 |
| rs201681439 | in-del | -/TATTT | | | intron-variant | USP30 | GRCh38.p7 | 12:109035373 | TATTTTATTTTATTT[-/TATTT]ATTTATTTTGAGATG | 84749 |
| rs201783676 | snp | C/T | 1.6757e-05 | 0.00289452 | intron-variant | USP30 | GRCh38.p7 | 12:109071572 | TGATCTTGCTCTTGC[C/T]TCTTCCAACCTCTCT | 84749 |
| rs201792052 | in-del | -/A | | | intron-variant | USP30 | GRCh38.p7 | 12:109078612 | CAAAAAAAAAAAAAA[-/A]GAGTTGCCTTCTCTT | 84749 |
| rs201840576 | snp | C/T | 0.000239464 | 0.0109396 | intron-variant | USP30 | GRCh38.p7 | 12:109084927 | CACTGCTAATTTTCA[C/T]TGACTCGGGCCTTTT | 84749 |
| rs201897738 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109080669 | TAGAACTTCCAACTA[C/T]AGTCATGTGCTATAT | 84749 |
| rs201938002 | in-del | -/ATATA | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055396 | TATATATATATATAT[-/ATATA]TTTTTTTTTTTTTTT | 84749 |
| rs201984497 | snp | C/T | 0.000391696 | 0.0139891 | intron-variant, missense | USP30 | GRCh38.p7 | 12:109083072 | CACCAGGTGTGTGCG[C/T]GCGAGGAGCCGATGC | 84749 |
| rs202039421 | in-del | -/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109041281 | TAACAACAAATAGGA[-/G]GAAACATGCACAATT | 84749 |
| rs202136105 | snp | A/G | 3.29609e-05 | 0.00405948 | missense, synonymous-codon, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088400 | GGGAATCCTTATGCC[A/G]GAAGACAAAGTCTCT | 84749 |
| rs202144827 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109023990 | TCCTTCAAAGGAAAA[A/G]GGGAGTTTGCAGCCT | 84749 |
| rs202236276 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | USP30, USP30-AS1 | GRCh38.p7 | 12:109054528 | GAGCAAGACACTGTC[C/T]CAAAAAAAAATAAAA | 84749 |
| rs207473359 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109056930 | TCAGGTTTTCAAACA[C/G]TACTTTTACCGTTAG | 84749 |
| rs367566462 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | USP30 | GRCh38.p7 | 12:109081990 | TCATCAGAATCAGTG[C/T]GGGATGTTGTGTGTG | 84749 |
| rs367618286 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | USP30, SVOP | GRCh38.p7 | 12:109021147 | TTCTGCTTGGAAGAG[C/T]TCACAGGCTCTCTGG | 84749 |
| rs367651909 | in-del | -/ACAC | | | intron-variant | USP30 | GRCh38.p7 | 12:109081607 | TGGCTTTTTGAATAC[-/ACAC]GCACGCATGCGCGCA | 84749 |
| rs367719967 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109047053 | TATTTCATTGACTAG[C/G]GTGACCACGTATTTG | 84749 |
| rs367725702 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109058199 | GAGTTAATACCTTAT[G/T]GTAGGAAAAGATCAT | 84749 |
| rs367754490 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109024406 | GGGATTACAGGTGTG[C/T]GCCACCATGCCAGGC | 84749 |
| rs367982832 | snp | C/G | 6.59109e-05 | 0.0057403 | intron-variant | USP30 | GRCh38.p7 | 12:109081401 | CCACATGGGTATGTA[C/G]TGATTTATGGTTTAT | 84749 |
| rs368041743 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109057419 | CAGAAGAGAGAAGTA[G/T]ATTAGATTTCATTGA | 84749 |
| rs368134668 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109041889 | AAAAAATAGTTTGAA[C/T]TACAAAGATTGTGAC | 84749 |
| rs368139119 | snp | G/T | 1.64825e-05 | 0.00287071 | missense, intron-variant | USP30 | GRCh38.p7 | 12:109058056 | CTCCAGGGATCAGAA[G/T]GAGCCCCCCTCACAC | 84749 |
| rs368189874 | snp | C/T | 4.95708e-05 | 0.00497825 | missense | USP30 | GRCh38.p7 | 12:109085034 | TGCCAACGCTGTCAG[C/T]GCCGATGCCCTTCCC | 84749 |
| rs368198239 | snp | A/G | 5.01593e-05 | 0.00500771 | intron-variant | USP30 | GRCh38.p7 | 12:109071580 | CTCTTGCCTCTTCCA[A/G]CCTCTCTAAAGAATG | 84749 |
| rs368241694 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109057624 | AAGAGAAAAAGACAG[A/G]AGATGGTTACTAAGT | 84749 |
| rs368283086 | snp | C/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109087993 | CTGCTGTGTATTATA[C/G]CAATAAAATAATCAT | 84749 |
| rs368292115 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109033119 | CCCATGGACTTAAAT[C/T]CAAAAAATGGATTTG | 84749 |
| rs368340022 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109082097 | ACACCAGTGACCCTG[A/T]GCTCTTCTGACTGTA | 84749 |
| rs368580113 | snp | C/G | 6.90572e-05 | 0.0058757 | intron-variant | USP30 | GRCh38.p7 | 12:109057888 | AAATTGATCAAATGT[C/G]ATATACTGTTCTCTT | 84749 |
| rs368590715 | snp | A/G | 5.22025e-05 | 0.00510867 | intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088518 | ATCTTTATACCTGCA[A/G]TGAGAAAACAAACAC | 84749 |
| rs368761274 | snp | G/T | 1.72036e-05 | 0.00293283 | intron-variant | USP30 | GRCh38.p7 | 12:109082652 | GCAGAGAAATGTTCC[G/T]TTTATTTCAGATTGA | 84749 |
| rs368819796 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109042831 | TGTTTTCAGATGATA[C/T]GATTTCATATGCAGA | 84749 |
| rs368834907 | snp | A/C/G | 6.59482e-05 | 0.00574198 | intron-variant | USP30 | GRCh38.p7 | 12:109067643 | GTGAGTACAACATTT[A/C/G]AACAGGTTTAGCTTG | 84749 |
| rs368906505 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109059586 | TAGCACGATCTCAGC[C/T]CACTGCAACCTCCGC | 84749 |
| rs369017321 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053256 | AGTACCGCCCCCTAT[C/T]CCTGTTAGCCCGCCC | 84749 |
| rs369021692 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022450 | TCTCACATCGAATCC[A/G]TAAAAGGACTTGAAA | 84749 |
| rs369032252 | snp | A/G/T | 5.04664e-05 | 0.00502301 | intron-variant | USP30 | GRCh38.p7 | 12:109082789 | TGTTTTGAGGACTCC[A/G/T]TGTATCCTGCCCCTG | 84749 |
| rs369047786 | snp | A/G | 0.00109479 | 0.0233708 | intron-variant, missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052692 | CAATGCTGAGCTCCC[A/G]GGCCGAGGCGGCGAT | 84749 |
| rs369116078 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109067142 | TTTTTGAGATGGAGC[A/G]TCACTCTGTCACCCA | 84749 |
| rs369173755 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109084560 | TCAACATCCTCTAAT[C/G]CACAGGACAGCCCCC | 84749 |
| rs369179779 | snp | G/T | 3.31664e-05 | 0.00407211 | missense | USP30 | GRCh38.p7 | 12:109082728 | CACTTTTGTTAAACA[G/T]TTAAAACTAGGGAAG | 84749 |
| rs369263537 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109079328 | TTTTTCTCTTTTTTT[C/T]TTTTCTTTTTCTTTT | 84749 |
| rs369310652 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109045500 | GAGGCAGAATTGTCC[A/C]GCTTAAGACACAGGC | 84749 |
| rs369320593 | snp | C/T | 6.64319e-05 | 0.00576295 | intron-variant | USP30 | GRCh38.p7 | 12:109072365 | GGTAGCTGTTTTCCA[C/T]TGAAATATAACACAT | 84749 |
| rs369480328 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109074947 | TTTCTAGATTCCATA[C/T]AGGTATGAGATCAGG | 84749 |
| rs369487038 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109036121 | GTCAGGGTTTCACCA[C/T]TGCACTTAAGCTTGG | 84749 |
| rs369508238 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109068018 | CATTTTTTAAAAAAT[C/T]AATCTTCGGAGCTTT | 84749 |
| rs369533795 | in-del | -/GTTT | | | intron-variant | USP30 | GRCh38.p7 | 12:109030629 | CTTGTTTGTTTGTTT[-/GTTT]TTTGAGACGGAGTCT | 84749 |
| rs369599730 | snp | A/G | | | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109021294 | TCATTAATGTTATCC[A/G]TATAACACTCTTGAA | 84749 |
| rs369664126 | snp | A/G | 5.75291e-05 | 0.00536295 | intron-variant | USP30 | GRCh38.p7 | 12:109071753 | CTGTGCAGCTTGTGC[A/G]TATTTAATAAGTATA | 84749 |
| rs369816709 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109062989 | CTCATTAAGCGGACT[A/C]ATATAATATTCACCC | 84749 |
| rs369833455 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon | USP30 | GRCh38.p7 | 12:109085805 | TCAGTGGCTGTGGGT[C/T]TCCGATGACACTGTC | 84749 |
| rs369885613 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109030071 | CATGTTCACCTTCTT[C/T]CTGCAAGTTACGCTG | 84749 |
| rs369893565 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109025389 | TTGGTTTTGTCTATC[C/T]GGAGAGCTCTGACTA | 84749 |
| rs369936245 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109069497 | ATCTCTACTTCCACT[C/G]TACAGCTGCAGTTTT | 84749 |
| rs370010699 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109056854 | CCTGTTATCTGAAAA[C/T]AGTACAAAGAAGGTG | 84749 |
| rs370016965 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109032014 | GACTAAGGTAGGAGG[A/C]TCACTTGAGCCTAGG | 84749 |
| rs370070834 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109077821 | TACTCTTGTGTGTTT[G/T]TGTTGGGGGGGGAGG | 84749 |
| rs370220358 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | USP30 | GRCh38.p7 | 12:109072367 | TAGCTGTTTTCCATT[A/G]AAATATAACACATAA | 84749 |
| rs370250597 | in-del | -/A | | | intron-variant | USP30 | GRCh38.p7 | 12:109044713 | CCACAATAAAAAAAA[-/A]TGGAAAAATCCTCTC | 84749 |
| rs370325927 | snp | C/T | 1.66988e-05 | 0.00288949 | missense, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088477 | TCTCTTTCATCATCT[C/T]GGTGCTCCCCGATGT | 84749 |
| rs370330131 | snp | G/T | 1.67806e-05 | 0.00289656 | intron-variant | USP30 | GRCh38.p7 | 12:109056817 | GAACACTGCATCATG[G/T]TCTGTAGACTTGACC | 84749 |
| rs370401335 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109040697 | GGCTGTTGGCAGAAG[A/G]CCTCAGTTCCTTGCC | 84749 |
| rs370409873 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109070360 | GCTTTGGATAATTGG[C/T]TGGGGAGTATGCCCT | 84749 |
| rs370437661 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109026329 | GATCCACCCGCCTTG[A/G]CCTCCCAAAGTGCTG | 84749 |
| rs370455010 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109084220 | GCAACAGAGCAAGAT[C/T]CTGTCTAAAACACAC | 84749 |
| rs370481664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109023231 | GCTCTCTAGGGCTCT[A/G]TGAATATTCATTATG | 84749 |
| rs370488419 | snp | C/T | 9.89903e-05 | 0.00703458 | intron-variant | USP30 | GRCh38.p7 | 12:109081882 | ATCTGCTAACAGTTT[C/T]AGTATAGCTGTCCTT | 84749 |
| rs370505505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109064214 | AGAAGTTCTGAGTTC[A/G]TATATTCTGGGTATT | 84749 |
| rs370511348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109028517 | AGTTTCCCTCTTGTC[A/G]CCCAGACTGGAGTGC | 84749 |
| rs370512901 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109037727 | CCTTAAATGCCTGGA[A/G]CTGCCTGGAACCAGT | 84749 |
| rs370613491 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088305 | CCAGTGCGTGTTGGT[C/T]GGGTGGTTCATCATT | 84749 |
| rs370658959 | snp | A/G | 3.52175e-05 | 0.00419613 | missense | USP30 | GRCh38.p7 | 12:109085911 | CAGCACCAGAGCCAG[A/G]AGTGCAAGTCTGAAG | 84749 |
| rs370667057 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109038204 | GTGTATGTTGGTTCC[C/T]GCCCCCCTCCCCACC | 84749 |
| rs370667369 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109070521 | GAATGTTGGGGGCTT[C/T]GTAGGCCAGATAAGA | 84749 |
| rs370671896 | snp | A/G | 4.94262e-05 | 0.00497098 | missense | USP30 | GRCh38.p7 | 12:109081340 | TTCTTTCAGAGTCCT[A/G]TTCGATTTGATACCT | 84749 |
| rs370678568 | snp | A/C | 0.000332428 | 0.0128881 | intron-variant, missense, utr-variant-5-prime, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052752 | TCCTGCGGACCGGGG[A/C]GGCCGTCAGGTGAGA | 84749 |
| rs370788043 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109081699 | AGATACCTAAAACAG[A/C/T]GTGGAAGTCCACAAG | 84749 |
| rs370825027 | snp | C/T | 1.70942e-05 | 0.00292349 | intron-variant | USP30 | GRCh38.p7 | 12:109084931 | GCTAATTTTCATTGA[C/T]TCGGGCCTTTTTCTC | 84749 |
| rs370849464 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109050937 | GCTTGAACCTGAGAG[G/T]CGAGATCGTGCCATT | 84749 |
| rs370944335 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109065468 | CACAAAGTGTGAAGG[C/T]GGCTGTCTGGGGACA | 84749 |
| rs371013818 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109078293 | GCTGGGCCTGGTGGC[A/G]GGCGTCTGTAATCCC | 84749 |
| rs371122307 | snp | C/T | 0.000197984 | 0.0099475 | missense | USP30 | GRCh38.p7 | 12:109082898 | GGTCCAGCCACGGCA[C/T]GCCTCTGAAGCGGCA | 84749 |
| rs371201948 | snp | A/G | 4.1806e-05 | 0.00457179 | downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088166 | CTCCCTCTTAGAGTC[A/G]AGAGGGAAAGAGAAA | 84749 |
| rs371252443 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109047300 | TTGTCTGGGGAGAAG[C/G]GTGAATCAGTGCTAA | 84749 |
| rs371265549 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109024239 | TAAGTGTTAGCTGTT[A/G]CAATGGTTAAATTAA | 84749 |
| rs371336695 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109023716 | TCGGCTCACTGCTAC[C/T]TCCACCTCCCGGATT | 84749 |
| rs371434630 | snp | C/T | | | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109087299 | CATCTGAGGTAAGGC[C/T]AAGACCGCACTTCCT | 84749 |
| rs371443722 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | USP30 | GRCh38.p7 | 12:109028472 | TTTTTCTGTTTTTTT[G/T]TTGTTGTTGTTGTTT | 84749 |
| rs371447272 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | USP30 | GRCh38.p7 | 12:109082025 | CTGTACAAAGGTATG[A/C]ATTGAACCCCAAATG | 84749 |
| rs371452678 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109061649 | TCCTAAGCTCAAGCA[A/G]TCTGCCTGCCTTGGC | 84749 |
| rs371471606 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109051382 | CCGCCTCAGCCTCCC[C/G]AGTAGCTGGGATTAC | 84749 |
| rs371479492 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109080051 | TACATTGGGCAGCAA[A/G]ATCTCTGCTCAGTTT | 84749 |
| rs371577912 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109031164 | AGATAAACATGTTCA[A/G]TGTCTATTTAAAATT | 84749 |
| rs371623412 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109069836 | GGAGGTGAGGTTTCA[A/G]CGGAGACCGGAAGTA | 84749 |
| rs371753407 | snp | A/C | 0.000955645 | 0.0218382 | intron-variant | USP30 | GRCh38.p7 | 12:109081910 | CTTTGAATTGTAGTA[A/C]TTTTCTTCTTCTCAT | 84749 |
| rs371828004 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109034436 | CTTGAGAAGAAAGTG[C/T]ATTCTGTAGGCCAGG | 84749 |
| rs371844460 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109056256 | GGAGTGCAATGGCAC[A/G]ATCTCAGCTCTGTGC | 84749 |
| rs371920523 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant | USP30 | GRCh38.p7 | 12:109057972 | CACCTGCTTCATGAA[C/T]TCCCTGCTACAAGGC | 84749 |
| rs372032444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109047829 | CCTCTGCCTCTACAA[A/G]AAATACAAAAAATTA | 84749 |
| rs372059149 | snp | A/G | | | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109021322 | GAAACCCAGGCTGCT[A/G]TAACAAATACAGGCA | 84749 |
| rs372059438 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109082570 | AGCAGTCAAGTGCCA[A/G]TTGTGTGCCGCTATA | 84749 |
| rs372071106 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109029005 | TAATTAAAATGTTGG[C/T]TTGTTGTGGTCCTTA | 84749 |
| rs372072399 | snp | C/G | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | USP30, USP30-AS1 | GRCh38.p7 | 12:109052299 | CTGACCCGACTTTCG[C/G]CTGTTGGCCTCCCTT | 84749 |
| rs372156919 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109040844 | GCTTTGGAATTCACA[G/T]AGCATCACTCTCACA | 84749 |
| rs372168079 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109081618 | ATACACACGCACGCA[C/T]GCGCGCACACACACA | 84749 |
| rs372272675 | snp | A/G | 4.95119e-05 | 0.00497529 | intron-variant | USP30 | GRCh38.p7 | 12:109067496 | ATGCTGATGAATTTA[A/G]TAATTGTCTTACCTT | 84749 |
| rs372325099 | snp | G/T | 1.65594e-05 | 0.0028774 | missense | USP30 | GRCh38.p7 | 12:109082688 | AGGGAACGTTGAACG[G/T]GGAAAAGGTGGAACA | 84749 |
| rs372337885 | snp | A/T | 1.70571e-05 | 0.00292032 | intron-variant | USP30 | GRCh38.p7 | 12:109057906 | ATACTGTTCTCTTCT[A/T]CCCCCTGCTTTTTTT | 84749 |
| rs372390606 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109059167 | ACTGGCTTGGTAAAG[A/G]TTTTAAGAAATAACC | 84749 |
| rs372390768 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109039203 | GATTTTTCTCCGTTT[-/T]CCTCAGAAAGTTTTA | 84749 |
| rs372507116 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109083558 | GGTAGCTATTATCGC[C/G]GGTCTTACTGATAAG | 84749 |
| rs372549231 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109079333 | CTCTTTTTTTCTTTT[C/T]TTTTTCTTTTTTTTT | 84749 |
| rs372589060 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109069371 | CCCTGCTTCCTGTTC[A/C]TCTGTACAGGGCTGC | 84749 |
| rs372667971 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109031291 | ACAGTTTCATTCAAA[C/T]TCTACACATGTGTCC | 84749 |
| rs372673295 | snp | C/G/T | 0.000621501 | 0.017619 | intron-variant | USP30 | GRCh38.p7 | 12:109082822 | ACAACTCGGTTCTCC[C/G/T]GATTTCTCTTCCACC | 84749 |
| rs372678815 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109040388 | TTTTGAGGTAGTTGG[A/T]ATAAAGTCCACATTT | 84749 |
| rs372685212 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109066641 | AGTGAGCTGAGATCA[C/T]GCCATTGCACTCCAC | 84749 |
| rs372704137 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109049972 | AAAATGCAGTATCTT[C/T]GAAGCACAATAAAGT | 84749 |
| rs372711001 | snp | C/T | | | intron-variant, missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052713 | AGGCGGCGATGACCG[C/T]GGCCGACAGGGCCAT | 84749 |
| rs372795932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109082192 | GACCAAATCTCTTTC[C/T]CAGATGAGTTTTGTT | 84749 |
| rs372825500 | snp | C/T | | | downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088155 | GGAAATGCCAGCTCC[C/T]TCTTAGAGTCGAGAG | 84749 |
| rs372851045 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109033422 | GTAACATTAGTCTTC[A/G]AGTCACAGCAGGTTG | 84749 |
| rs372872485 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109071971 | TTATTTTTTCCTGTT[C/T]AATACAGGGGAACAG | 84749 |
| rs372881251 | snp | G/T | | | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022660 | TGGACTTAAAACCCC[G/T]GCAGTCTATCTCCAC | 84749 |
| rs373005101 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109063874 | CATTTTTGAATTGGG[-/T]TTTCTTTTTTTTTTT | 84749 |
| rs373028321 | snp | C/T | 0.000131872 | 0.00811902 | intron-variant | USP30 | GRCh38.p7 | 12:109085655 | CCCCTGACATGTGTT[C/T]GTATCATTCAGCTCC | 84749 |
| rs373104004 | snp | G/T | 3.33539e-05 | 0.00408361 | intron-variant | USP30 | GRCh38.p7 | 12:109071591 | TCCAACCTCTCTAAA[G/T]AATGCTTTGCCCTAT | 84749 |
| rs373144685 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109039257 | TCTATAATTCATTTC[A/T]AGTTAATTTGCATGT | 84749 |
| rs373152566 | in-del | -/GC/GCGC | | | intron-variant | USP30 | GRCh38.p7 | 12:109081618 | TACACACGCACGCAT[-/GC/GCGC]GCGCGCACACACACA | 84749 |
| rs373199260 | snp | A/G | 7.31676e-05 | 0.00604801 | intron-variant, missense | USP30 | GRCh38.p7 | 12:109083083 | TGCGCGCGAGGAGCC[A/G]ATGCAGCAGGAATTT | 84749 |
| rs373220366 | snp | A/G | 0.000117126 | 0.00765176 | missense, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088232 | TAAGCAAAATTTTAC[A/G]AAAAGTCAGATTCAC | 84749 |
| rs373293104 | snp | C/T | 0.000153988 | 0.00877328 | missense | USP30 | GRCh38.p7 | 12:109085872 | GCCTACCTGCTGTTC[C/T]ACGAGCGCGTCCTTT | 84749 |
| rs373346653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109043052 | TAACCAAGGAAGTGA[A/G]AGACTTTTACAATGA | 84749 |
| rs373364978 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109044783 | ATACTTTGTCACTGA[A/G]TATGCAGATTTGTAA | 84749 |
| rs373483615 | snp | A/G | 6.66378e-05 | 0.00577187 | intron-variant | USP30 | GRCh38.p7 | 12:109082752 | AGGGAAGGTGAGCCC[A/G]CACTACACACCCTGT | 84749 |
| rs373604786 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109026796 | CTAACAGTTCTAGAG[A/G]CTGACAAGTTCAAGA | 84749 |
| rs373635241 | snp | C/T | | | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109087410 | TCTGCTGGGCCCAGG[C/T]TGCACCCTGAGGACT | 84749 |
| rs373641992 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109068308 | CCAGCTTCGTGTAGG[C/T]GTTGTCTGCCGCCAC | 84749 |
| rs373676669 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109024666 | GCTCTGTCTCCCAGG[C/T]TGGAGTGCAGTGGCG | 84749 |
| rs373686187 | snp | A/C/G | 0.000131777 | 0.00811619 | missense | USP30 | GRCh38.p7 | 12:109081972 | TGCCTTCACCACTTC[A/C/G]TCTCATCAGAATCAG | 84749 |
| rs373699872 | in-del | -/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109076425 | CTTTTTTTTTTTTTT[-/C]TTTGCCTTATTATCC | 84749 |
| rs373738386 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109030925 | GGCCGATTGTGATTC[C/T]TTTACAATGTACACA | 84749 |
| rs373757433 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109063528 | TGAACATTAGTGTCC[A/C]AATTCCCTGCTTTCA | 84749 |
| rs373780818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109084332 | GCCTTAATTATGTTG[C/T]CTACCCATAAACATG | 84749 |
| rs373815156 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109056501 | CCCAGCTGACTTAGA[C/T]TTTAAATCCTAATGT | 84749 |
| rs373893551 | snp | A/G | 3.29951e-05 | 0.00406159 | intron-variant | USP30 | GRCh38.p7 | 12:109081883 | TCTGCTAACAGTTTC[A/G]GTATAGCTGTCCTTT | 84749 |
| rs373915334 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109028755 | GTGCTGGGATCACAG[A/G]CATGAGCCACCACAC | 84749 |
| rs373921085 | in-del | -/A | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | USP30, USP30-AS1 | GRCh38.p7 | 12:109054537 | CTGTCTCAAAAAAAA[-/A]ATAAAAATAAAAATA | 84749 |
| rs373924577 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | USP30 | GRCh38.p7 | 12:109067275 | CCCACCACCACGCCC[A/G]GCTAATTTTTTTTTT | 84749 |
| rs373949085 | in-del | -/GATA | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109045855 | CGTATAGATCATATA[-/GATA]CAGACATAGACACAT | 84749 |
| rs374069347 | in-del | -/TGT | 0.00159672 | 0.0282102 | intron-variant | USP30 | GRCh38.p7 | 12:109082792 | TTGAGGACTCCGTGT[-/TGT]ATCCTGCCCCTGAAA | 84749 |
| rs374130319 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109032293 | TGGGAGATAGAATGA[C/T]ACTGTCTAAAAAACA | 84749 |
| rs374266014 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109065918 | TTTGTGCTGCAGTGG[C/T]AGAGTTGAGTAGTTG | 84749 |
| rs374303861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109042774 | GGCAAGAAAAAGACA[C/T]AAAAGGCATCCAAAT | 84749 |
| rs374317590 | snp | A/G/T | 0.000955663 | 0.0218423 | missense, synonymous-codon, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088332 | CATTAGTAAGCTCCC[A/G/T]TGGGCCAGCGGCAGC | 84749 |
| rs374348235 | snp | A/C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109057308 | TCATTGTTAAATCTG[A/C/G]GGACAGTTATAATTG | 84749 |
| rs374480935 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109050962 | GCCATTGCACTGCAG[C/G]CTGGGCGGCAGAGCA | 84749 |
| rs374521130 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109035370 | TTTTATTTTATTTTA[-/T]TTTATTTATTTTGAG | 84749 |
| rs374588454 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109064359 | AATCTCTGCCTCCAG[A/G]GTTCAAGTGATCCTC | 84749 |
| rs374617622 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109056483 | CAGGGATGAGCCACC[A/G]TGCCCAGCTGACTTA | 84749 |
| rs374830297 | in-del | -/G | 0.283561 | 0.247737 | intron-variant | USP30 | GRCh38.p7 | 12:109077825 | TTGTGTGTTTGTGTT[-/G]GGGGGGGGAGGGTGT | 84749 |
| rs374887435 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109077569 | TGACTTTGTGGACAG[C/T]ATATAATGGGTCTTG | 84749 |
| rs375013273 | in-del | -/TC | | | intron-variant | USP30 | GRCh38.p7 | 12:109044987 | AAGTAAGGTCAAACA[-/TC]TTTTTTTTTTTTTTT | 84749 |
| rs375077503 | snp | G/T | 8.23621e-05 | 0.00641672 | synonymous-codon | USP30 | GRCh38.p7 | 12:109085742 | TGGACACTTTGTCAC[G/T]TACCGACGGTCCCCA | 84749 |
| rs375132475 | snp | C/G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109024643 | TTTTTTTCCCGAGAC[C/G/T]GAGTCTCGCTCTGTC | 84749 |
| rs375138710 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109042487 | CTCCTATTTTCTCTT[A/G]ACAAAACATCTGAGC | 84749 |
| rs375142732 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022145 | TATAGATGTGAGCCA[C/T]TGCGCCCGGCCTCAG | 84749 |
| rs375145793 | snp | A/G/T | 4.95163e-05 | 0.00497555 | missense | USP30 | GRCh38.p7 | 12:109082894 | AGCTGGTCCAGCCAC[A/G/T]GCACGCCTCTGAAGC | 84749 |
| rs375191817 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109067281 | ACCACGCCCGGCTAA[A/T]TTTTTTTTTTTATTT | 84749 |
| rs375206887 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109076772 | AGTCTTGCTCTGTCG[A/C]CCAGGCTGGAGTGCA | 84749 |
| rs375227341 | snp | G/T | | | utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109024848 | ATGGTCTCGATCTCC[G/T]GATCTCGTGATCCAC | 84749 |
| rs375274391 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109025212 | AATTTGGCCCAGCAT[C/T]CCAGGGTTTCTAGCT | 84749 |
| rs375285148 | snp | C/T | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | USP30, USP30-AS1 | GRCh38.p7 | 12:109052293 | AGAGGCCTGACCCGA[C/T]TTTCGGCTGTTGGCC | 84749 |
| rs375289510 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109049534 | ATGAAAAACTTTGGG[A/T]CCAGGCACGGTGGCT | 84749 |
| rs375290579 | snp | G/T | | | intron-variant, stop-gained | USP30 | GRCh38.p7 | 12:109083152 | GGGTCCCTTATGACA[G/T]GAGCACAAGGCTTGT | 84749 |
| rs375296825 | snp | C/T | 1.66913e-05 | 0.00288883 | intron-variant | USP30 | GRCh38.p7 | 12:109082758 | GGTGAGCCCACACTA[C/T]ACACCCTGTTGGCTT | 84749 |
| rs375300005 | in-del | -/ATCT | | | intron-variant | USP30 | GRCh38.p7 | 12:109039149 | TTTGTGCTTTTTGTG[-/ATCT]ATCTATGAAATCTTT | 84749 |
| rs375338036 | snp | A/G | 1.65663e-05 | 0.002878 | intron-variant | USP30 | GRCh38.p7 | 12:109067676 | GAATCCTTTCCCCTA[A/G]TGACTTGGGGCCTGA | 84749 |
| rs375445256 | in-del | -/A | 0 | 0 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | USP30, USP30-AS1 | GRCh38.p7 | 12:109054538 | TGTCTCAAAAAAAAA[-/A]TAAAAATAAAAATAA | 84749 |
| rs375521369 | snp | A/G | 1.65627e-05 | 0.00287769 | missense | USP30 | GRCh38.p7 | 12:109082687 | AAGGGAACGTTGAAC[A/G]GGGAAAAGGTGGAAC | 84749 |
| rs375692939 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046335 | GGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT | 84749 |
| rs375738354 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109043700 | GACACCAAAGACACA[C/G]GCAACAACAACAAAA | 84749 |
| rs375745235 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109039432 | CTAGTCATTTGACCT[-/T]AGATAAAGTTCCTAC | 84749 |
| rs375784806 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109066499 | ACCAGCGTGGCCAAC[A/C]TGGGGGAACCCCCAT | 84749 |
| rs375796760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109023382 | ACATGGCAAAACCTC[A/G]TCTCCACTTGAAAAT | 84749 |
| rs375813428 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109059501 | ACGCCTGGCCCCAAC[C/T]TCATTTTTATTTTTA | 84749 |
| rs375879392 | snp | C/T | 8.93503e-05 | 0.00668335 | intron-variant | USP30 | GRCh38.p7 | 12:109071734 | TTAATATTTCCAACA[C/T]GTTCTGTGCAGCTTG | 84749 |
| rs375883928 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP30 | GRCh38.p7 | 12:109024561 | CCGTGCCCGGCCACA[A/G]TGATTAATTTTAAGT | 84749 |
| rs375914739 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109030485 | CAAAGTTTCTTTCAT[A/T]TATACAAGATGAATA | 84749 |
| rs375964832 | snp | C/T | 1.68801e-05 | 0.00290512 | intron-variant | USP30 | GRCh38.p7 | 12:109056831 | GGTCTGTAGACTTGA[C/T]CCAGATCCCTGTTAT | 84749 |
| rs375965054 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046856 | TGTGCGCCATCATGC[C/T]CAGCTAATTTTTGTA | 84749 |
| rs375973071 | snp | C/G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109023253 | TTCATTATGCTCACT[C/G/T]TAAACAGCCCTCTTA | 84749 |
| rs375979876 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109023749 | AGCAATTCTCTGCCT[C/T]GGCCTCCCAAGTACC | 84749 |
| rs375992472 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | USP30, SVOP | GRCh38.p7 | 12:109021234 | CGGGTACCAGTGAGC[A/G]CCCTTTGATTGACGA | 84749 |
| rs376000521 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109078403 | CACTTCAGTCTGGGC[A/G]ACAGAGTGAGACTGA | 84749 |
| rs376101221 | in-del | -/A | 0 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109058587 | AAAAAAAAAAAAAAA[-/A]TCAAAGATGGAACCA | 84749 |
| rs376122044 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109026216 | GAGTAGCTGGGACTG[C/T]AGGCGCATGCCATCA | 84749 |
| rs376204560 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109056618 | AATGTTATTCTGTCT[A/G]TATCTGTATATTTGC | 84749 |
| rs376325707 | snp | A/G | 0.000544352 | 0.0164888 | synonymous-codon | USP30 | GRCh38.p7 | 12:109082899 | GTCCAGCCACGGCAC[A/G]CCTCTGAAGCGGCAT | 84749 |
| rs376341015 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109068266 | ACAGGTGCATCCTCC[A/C]CAGCCACACTTCCAA | 84749 |
| rs376529752 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | USP30 | GRCh38.p7 | 12:109035003 | TACTTTTAACCTATT[C/T]GTGTCTATGAATCTG | 84749 |
| rs376550265 | snp | A/C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109035867 | ACAAAAAAATTATAT[A/C/G]CAAAAAATACATGGG | 84749 |
| rs376574080 | snp | A/T | 0.000248861 | 0.0111521 | missense, intron-variant | USP30 | GRCh38.p7 | 12:109058086 | CCAGTATTTATCCTT[A/T]ACACTCTTGCACCTT | 84749 |
| rs376621432 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109025174 | ACTTACATGTGTGGC[C/T]CCCTTGGGTTTTTGG | 84749 |
| rs376626837 | snp | A/C/T | 1.70327e-05 | 0.00291823 | intron-variant | USP30 | GRCh38.p7 | 12:109057907 | TACTGTTCTCTTCTT[A/C/T]CCCCTGCTTTTTTTT | 84749 |
| rs376631307 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109045033 | CCCAGGCTAGAGTGC[A/G]GTGGCGCAATCTCTG | 84749 |
| rs376660125 | snp | C/T | 1.64914e-05 | 0.00287149 | intron-variant | USP30 | GRCh38.p7 | 12:109082066 | CTGGCCTGTGTGTGC[C/T]GATGTAGCGCCTCTC | 84749 |
| rs376691745 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109038170 | TGCTCTCCCTCCCCC[A/G]ACCCCTCCAAAGGCC | 84749 |
| rs376697558 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109067100 | AAGGTTAATCCTACA[A/G]TCCTTAATTTTTTTT | 84749 |
| rs376716278 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109038224 | CCCTCCCCACCTGCC[A/C]GTTTCCATGTGTTCT | 84749 |
| rs376718724 | snp | A/G | | | intron-variant, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053766 | ATGTCATTTTGCAGA[A/G]GAATGGAGTTTCCAA | 84749 |
| rs376724299 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109030812 | GTAGAGAGAGGGTTT[C/T]ACCATCTTGGCCAGG | 84749 |
| rs376775701 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109024634 | CAGCATTTTTTTTTT[-/T]CCCGAGACCGAGTCT | 84749 |
| rs376930169 | in-del | -/G | | | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109021426 | ATTCGACCTGTCATT[-/G]TCATCGTGGAGCTAA | 84749 |
| rs376958672 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109084445 | TTGGAGGAGTTTTGC[A/C]TCCCAAGGGACATTG | 84749 |
| rs376997991 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109086183 | CGGAGTGTCTTTTTA[C/T]TCATCTGATACAGGT | 84749 |
| rs377001562 | snp | C/T | 0.000378878 | 0.0137585 | missense | USP30 | GRCh38.p7 | 12:109081337 | TATTTCTTTCAGAGT[C/T]CTGTTCGATTTGATA | 84749 |
| rs377043552 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109084175 | TGAGGCTGCAGTGAG[C/T]TGTGATCACACCACT | 84749 |
| rs377086341 | in-del | -/TCTT | 0.0111196 | 0.0737302 | intron-variant, utr-variant-3-prime, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109087735 | ATGGTTATAAGCAGA[-/TCTT]TCTTTCTTTGGTCAG | 84749 |
| rs377087654 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109025991 | ACCCTGGCATGAAGC[A/G]TTTTTTAAGTTGTAA | 84749 |
| rs377110873 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | USP30 | GRCh38.p7 | 12:109047722 | TGTGTTGGGTAAGTG[G/T]GGCATTTAAAGAGAG | 84749 |
| rs377141587 | snp | A/G | 1.65512e-05 | 0.00287669 | missense | USP30 | GRCh38.p7 | 12:109082693 | ACGTTGAACGGGGAA[A/G]AGGTGGAACACCAGA | 84749 |
| rs377150426 | snp | C/G/T | 8.33779e-05 | 0.00645626 | synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088239 | AATTTTACGAAAAGT[C/G/T]AGATTCACCCGTGGA | 84749 |
| rs377249699 | in-del | -/TTGTTTT | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109047444 | ACATTTATTATTGTT[-/TTGTTTT]GGCCCCCAAAACAAC | 84749 |
| rs377423693 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109079320 | CTGATTCTTTTTTCT[C/T]TTTTTTTCTTTTCTT | 84749 |
| rs377428084 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109040411 | CCACATTTTGAGGAA[C/T]ATTGCTCCTGCTATA | 84749 |
| rs377462816 | snp | A/T | 0.000240732 | 0.0109685 | intron-variant | USP30 | GRCh38.p7 | 12:109084902 | CAAAACCAGGTTTTG[A/T]TTACAGAGCCACTGC | 84749 |
| rs377463507 | snp | C/T | 1.66801e-05 | 0.00288787 | intron-variant | USP30 | GRCh38.p7 | 12:109082840 | TTTCTCTTCCACCCG[C/T]AGCTCCCTCAGTGTC | 84749 |
| rs377486660 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109060863 | TTTCACCAGGCTGCT[C/T]TCGAACTCCTGACCT | 84749 |
| rs377517085 | snp | C/G | 1.65318e-05 | 0.002875 | missense | USP30 | GRCh38.p7 | 12:109072339 | CCAAACAAATTACCT[C/G]CCGCACAAGAGGTAG | 84749 |
| rs377599084 | in-del | -/AC | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055015 | GGATAATAATGTATT[-/AC]ACACACACACACACA | 84749 |
| rs377655105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109078506 | TAAGAGGCTGAGGCA[A/G]GAGAATTGCTTGAAC | 84749 |
| rs377657690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109050921 | CTGAGGCAGGATAAT[C/T]GCTTGAACCTGAGAG | 84749 |
| rs377661586 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109026912 | TTCCTTGGCACATAA[A/G]CATAAAGAGAAAGCA | 84749 |
| rs377761475 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109080024 | TGGGCTCAAACTCAA[C/T]TCTGTCTCCCCTACA | 84749 |
| rs386377707 | in-del | -/A | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | USP30, USP30-AS1 | GRCh38.p7 | 12:109054532 | AGACACTGTCTCAAA[-/A]AAAAAATAAAAATAA | 84749 |
| rs386377708 | in-del | -/A | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | USP30, USP30-AS1 | GRCh38.p7 | 12:109054536 | ACTGTCTCAAAAAAA[-/A]AATAAAAATAAAAAT | 84749 |
| rs386377709 | in-del | -/A | | | intron-variant | USP30 | GRCh38.p7 | 12:109058573 | CGAAACTCCGTCTCA[-/A]AAAAAAAAAAAAAAT | 84749 |
| rs397812148 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109042211 | TGAGCTTTTTTTTTT[-/T]CCAAAAGGAATGTCA | 84749 |
| rs397973697 | in-del | -/AATA | | | intron-variant | USP30 | GRCh38.p7 | 12:109023578 | ATAAATAAATAAATA[-/AATA]GCCCCCTTATCATCC | 84749 |
| rs398021007 | in-del | -/A | 0 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109032113 | TCAAAAAAAAAAAAA[-/A]CACGGGCAACATGGT | 84749 |
| rs398021008 | in-del | -/T | 0 | 0 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109047181 | TGCATTTTTTTTTTT[-/T]AACCGAGGAAACCCT | 84749 |
| rs398021009 | in-del | -/A | 0 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109061410 | AAAAAAAAAAAAAAA[-/A]TTTTTTTTTTTTTTT | 84749 |
| rs398021011 | in-del | -/T | 0 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109076424 | CCTTTTTTTTTTTTT[-/T]CTTTGCCTTATTATC | 84749 |
| rs398021012 | in-del | -/T | 0 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109076749 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTTGC | 84749 |
| rs398098495 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109063117 | TTCTATTTTTTTTTT[-/T]AAGACAAAGTCTCAT | 84749 |
| rs527290523 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109056626 | TCTGTCTATATCTGT[A/T]TATTTGCCTTTTGTG | 84749 |
| rs527317897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109049773 | GTGAGCCAAGATTGC[A/G]CCACTGCACTCCAGC | 84749 |
| rs527449838 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109027143 | TAGTGGCTTAGAGTA[G/T]ATTCATAATGTTATA | 84749 |
| rs527466293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109070078 | CTATTGTGTTTGCAG[C/T]GGGGAGCCACTAGAG | 84749 |
| rs527477721 | snp | A/G | 0 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109078407 | TCAGTCTGGGCGACA[A/G]AGTGAGACTGAGTCT | 84749 |
| rs527570920 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109064950 | AACCCTGCTCCCTTT[G/T]TCCTGGGAGGGAAAG | 84749 |
| rs527632545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109041506 | CAGGCATGGTGGTGC[A/G]TGCCTGTTGTCCCAC | 84749 |
| rs527745214 | snp | A/G | 0.000102171 | 0.00714669 | intron-variant | USP30 | GRCh38.p7 | 12:109084934 | AATTTTCATTGACTC[A/G]GGCCTTTTTCTCTTG | 84749 |
| rs527758828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109034478 | ATGCCTGTAATCCCA[A/G]CGCTTTGGGAGACTG | 84749 |
| rs527834123 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109085570 | ATGGACTTACCATTG[A/T]ATTCATCCCCTATTT | 84749 |
| rs527878646 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054013 | AAGTGATAGTAGAAC[C/T]TGCATCTGTGGGGTT | 84749 |
| rs527922062 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | USP30, USP30-AS1 | GRCh38.p7 | 12:109054786 | GCCAGGATTGAACCA[G/T]AATAAGGTAATCCCA | 84749 |
| rs528010647 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109048192 | CTGGGCTCAAGCAAT[C/T]CTCCCACCTCAGCCT | 84749 |
| rs528043063 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109048836 | CGCAATCCTTGCTTG[A/G]CATGACCTTAGATCC | 84749 |
| rs528043437 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109025435 | TTATGTTGCTCTCTT[A/C]ACCCCCCAGCCCCCA | 84749 |
| rs528057282 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109032153 | CTCTACAAAAAAAAA[A/T]ATTACCTGGGCATGG | 84749 |
| rs528092568 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109025923 | AAACTCCTGGGCTCA[A/T]GGGATCCTCCCACCT | 84749 |
| rs528105920 | in-del | -/A | | | intron-variant | USP30 | GRCh38.p7 | 12:109061395 | TCTAACTTTGGTTTA[-/A]AAAAAAAAAAAAAAA | 84749 |
| rs528107876 | in-del | -/A | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109050989 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAGAATG | 84749 |
| rs528164606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109026402 | TTATTGTGGTAAATA[C/T]ATATGTCTTAGCCAG | 84749 |
| rs528167611 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109068408 | AGACTTTTGGAAAGG[C/G]AGCTGGGGAGGCTTT | 84749 |
| rs528186122 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | USP30 | GRCh38.p7 | 12:109040199 | AATTTAGGGTGCTAC[A/C]AAAATACCTGAAGTT | 84749 |
| rs528205994 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109069188 | AAGCTCCCCCTCCTC[A/T]GCAGTGCTGTCCCTT | 84749 |
| rs528207777 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109061711 | CACCATGCCTGGCCT[A/G]TAAATAATTTTTTAA | 84749 |
| rs528421154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109074837 | TCTCCAGAACTTATT[C/T]GTCTTATAACTGAAG | 84749 |
| rs528439817 | in-del | -/TTGTTG | 0.25214 | 0.249991 | intron-variant | USP30 | GRCh38.p7 | 12:109056176 | GATTTGACTTAGTTT[-/TTGTTG]TTGTTGTTGTTGTTG | 84749 |
| rs528444421 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109034480 | GCCTGTAATCCCAAC[A/G]CTTTGGGAGACTGAG | 84749 |
| rs528509497 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, nc-transcript-variant | USP30, USP30-AS1 | GRCh38.p7 | 12:109052543 | CCCCTGGGAGCTGTC[A/C]TGCGGTCTACGTTCC | 84749 |
| rs528617437 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046392 | TGCTGGGATTACGGG[C/G]GTGAGCCATTGCACC | 84749 |
| rs528666473 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109081814 | ATCCAGTTGTGACTA[C/T]AAAACTTTATTGCCT | 84749 |
| rs528681962 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109024049 | AGTCCTGGGGACTCT[C/T]TTCCCAGCTCCACCT | 84749 |
| rs528735616 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109066602 | AGGCAGGAGAATCGC[A/T]TGAACCCAGGAGGCG | 84749 |
| rs528772390 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109066986 | CATTTAAATGCTGCA[A/G]CCTCATGAAAAATTA | 84749 |
| rs528773199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109024547 | GCAGGCTTGAGCCAC[C/T]GTGCCCGGCCACAAT | 84749 |
| rs528856729 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109069393 | CAGGGCTGCACCTCT[A/G]GTGTGCCGTTGGCTA | 84749 |
| rs528859331 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109026473 | CACAACAGAATTTTT[C/T]TTTTTTTTGAGACAG | 84749 |
| rs528946810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109062519 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT | 84749 |
| rs528999929 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054954 | CTTCACCAAGTTAAT[A/G]TTTACTGAACTGAAA | 84749 |
| rs529067064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109083492 | TGCCTTCTGTACTGA[A/G]TTATGTATCTGATTC | 84749 |
| rs529102265 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109076193 | AAGTGGAATTTAAAA[A/C]AATTTATTTTCAAAT | 84749 |
| rs529108080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109084253 | AAAAAATGTCATCAG[A/G]AAACTACTTGGTACA | 84749 |
| rs529114887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109041189 | AATGTGCTGAAGACT[C/T]ATGGGATTTCTGTTT | 84749 |
| rs529180019 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109040070 | ATTAGAAAAATATTG[-/T]TTTTTTTCTACATGT | 84749 |
| rs529188322 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109025990 | GACCCTGGCATGAAG[A/C]GTTTTTTAAGTTGTA | 84749 |
| rs529239994 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109061537 | TTTCCATTTCCCAGG[G/T]AGCTGGGACTACAGG | 84749 |
| rs529415265 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109070895 | AACCCAAGTGTTCAT[C/T]GGCTGATAAATAGGT | 84749 |
| rs529469133 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109074655 | GAGATCTAATCGACA[A/G]TAAAAATTGTATATA | 84749 |
| rs529571623 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053102 | TAGGCCTGCCAAGAC[C/T]CCTCAATCCTTCTAG | 84749 |
| rs529593912 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109038479 | TTTAAGCTTTTTTTC[C/G]CTTTTAAGCTTTTTG | 84749 |
| rs529653590 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046055 | TCTGCAAGCAGAATT[C/T]CCTCTTATTCTTCCC | 84749 |
| rs529793616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109073906 | GAGAATTGTACAACT[A/G]TCACCCCAATCCATT | 84749 |
| rs529799602 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109023425 | CCAGGTGTGGTGGCA[C/T]AGACCTGTAGTCCCA | 84749 |
| rs529857143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109082579 | GTGCCAATTGTGTGC[C/T]GCTATAACACCACTG | 84749 |
| rs529862699 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109083488 | GAAATGCCTTCTGTA[C/T]TGAATTATGTATCTG | 84749 |
| rs529884396 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, downstream-variant-500B | USP30, USP30-AS1 | GRCh38.p7 | 12:109051731 | CCTGCCACCACGCCC[A/G]GCTAATTTTTGTATT | 84749 |
| rs529946072 | snp | C/T | 3.295e-05 | 0.00405881 | synonymous-codon | USP30 | GRCh38.p7 | 12:109085670 | CGTATCATTCAGCTC[C/T]TCCACATACCTCTTC | 84749 |
| rs529968855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109045526 | CAGGCCTTAGAATCA[C/T]ACAGACCCGCCTGCC | 84749 |
| rs530017578 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109066701 | AAAAAAAAGAAAAGT[A/G]CACTACTCAAAAGAC | 84749 |
| rs530020088 | snp | A/C | 0.000295623 | 0.0121542 | intron-variant | USP30 | GRCh38.p7 | 12:109072294 | CTGTTTTTTTTTTTT[A/C]TCCCCTACAGCAGCA | 84749 |
| rs530041405 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022830 | GTGGTACTCAAGCTC[C/T]AATGTATTATTTATC | 84749 |
| rs530181821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109072934 | TAAAGGCATTCCCAG[A/G]TCAGGTAGTGAATAA | 84749 |
| rs530186431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109043756 | ATTTAAAACTTTTGC[A/G]CATCAAAAGACACTA | 84749 |
| rs530228664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109066490 | GAGTTCGAGACCAGC[A/G]TGGCCAACATGGGGG | 84749 |
| rs530247179 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109086411 | TCGATTGCTTTTGTA[G/T]CACGTCCATTGTGAA | 84749 |
| rs530274732 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109034380 | GAGGCTTATTTTATG[G/T]CCTAATATATGGTCT | 84749 |
| rs530358137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109036249 | CCATGTGGGTTTGAA[C/T]TACTGTTAGTGCCCT | 84749 |
| rs530373823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109079522 | GTGTGTGCCACCACA[C/T]CCAGCTAATTTTTTT | 84749 |
| rs530385116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109031044 | TGTTCTGTCTTTACA[A/G]CTCTCCTGTAAATCC | 84749 |
| rs530393756 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | USP30 | GRCh38.p7 | 12:109028712 | AAACTCCTGACCTCA[G/T]GTGATCCACCCCCCT | 84749 |
| rs530400837 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109045167 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 84749 |
| rs530456750 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | USP30 | GRCh38.p7 | 12:109061170 | ACATTAGGATTAAAG[A/T]CAGGAGTATTCTTGG | 84749 |
| rs530480583 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053101 | CTAGGCCTGCCAAGA[A/C]CCCTCAATCCTTCTA | 84749 |
| rs530499572 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109085338 | TAAAGAAAATTTAAA[A/G]TTTCTTGGGATACCA | 84749 |
| rs530503538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109025390 | TGGTTTTGTCTATCC[A/G]GAGAGCTCTGACTAA | 84749 |
| rs530573381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109031600 | AGTGGAAGCAACCCA[C/T]GTGTCCATCAATAGA | 84749 |
| rs530593303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109074733 | TGTGCACGTGCACCT[A/G]TGCTCATATGTGGTG | 84749 |
| rs530651149 | snp | A/C | 0.00676609 | 0.0577691 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109086016 | TGTTGCGTGTGCAAG[A/C]GGCCCCACTAGAGCC | 84749 |
| rs530669878 | snp | A/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109087983 | ACTTTTGTATCTGCT[A/G]TGTATTATAGCAATA | 84749 |
| rs530734823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109039315 | CCTTCTATATTTTTA[C/T]GTGTCTTATCCTATA | 84749 |
| rs530842705 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046845 | AGGATTACAGGTGTG[C/T]GCCATCATGCCCAGC | 84749 |
| rs530873367 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109082193 | ACCAAATCTCTTTCC[C/T]AGATGAGTTTTGTTT | 84749 |
| rs530874473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109059300 | CTCAGGTTCAAGTGA[C/T]TCTTGTGCCTCAGCC | 84749 |
| rs530900485 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109023898 | TCGGCCTCCCAAAGT[G/T]CTGGGATTACAGGTG | 84749 |
| rs530973740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109037283 | TTTTAATAATCTCTA[C/T]CTCTTTATTAATATT | 84749 |
| rs531023198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109080334 | AAAGCCACAAACACA[C/T]AAATCTCGCCCACAG | 84749 |
| rs531039900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109059964 | AGAATGTAGATATCA[A/G]ACAGAATCATTAAGC | 84749 |
| rs531063806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109072440 | AAAGATTTTTTTCTG[A/G]TGACATACAGGCCAG | 84749 |
| rs531147270 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109076022 | TTGCTGTGTCATTGC[A/G]GTTCTGAGTGACATT | 84749 |
| rs531197055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109058470 | CCAGCTACTCAGGAG[A/G]CTGAGGCAGAAGAAT | 84749 |
| rs531218683 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022956 | AGTTGTCCCACCCAC[A/T]CTTATTTCTAAAGGA | 84749 |
| rs531331859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109087810 | GCAAAGCCTTTTAAC[C/T]TGACTTCTTCATTTT | 84749 |
| rs531370682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109044134 | ACAAATTACTGTATG[A/G]TTCCACTTATGTGAG | 84749 |
| rs531490967 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109057857 | GCGCAGGAACTCTGG[G/T]TCCCACATGGGAGAG | 84749 |
| rs531506110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109057721 | AAAGGGGACCTGTCC[C/T]TCTGTGCTTACAGTC | 84749 |
| rs531567450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109042641 | ACAATGTTACAGAAC[A/G]TTATACTCAATGGTG | 84749 |
| rs531691363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109034512 | TGGGAGGATCGCTTG[A/G]GCTCATGAGTTCAAG | 84749 |
| rs531879818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109079396 | TGACAGGGGTCTTAG[C/T]TCTGTCACCGAGGCT | 84749 |
| rs531931474 | snp | A/T | 0 | 0 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055730 | AACCTACTATGTGCT[A/T]AGTATGATCTAGACA | 84749 |
| rs531936561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109044836 | TCTACCTATACCTCT[C/T]ACAGAGATACCCAAG | 84749 |
| rs531969040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109048979 | GTATAAGGAGGCATG[C/T]CTGACCTCTCATCTC | 84749 |
| rs532022903 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109037474 | TTACTTTTTTTGTTT[C/T]TTCACATGTGTCATT | 84749 |
| rs532058875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109038328 | TGTCTCTGTCAAGGA[C/T]ATAATCTCATTCATT | 84749 |
| rs532087627 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB, downstream-variant-500B | USP30, USP30-AS1 | GRCh38.p7 | 12:109051693 | TCCTGCCTCAGCCTC[C/T]TGAGTAGCTGGAATT | 84749 |
| rs532127515 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109057133 | CATTTGTGTTCTCTC[A/G]GACTAGCTTGCTAGT | 84749 |
| rs532153727 | snp | C/T | 0.000412008 | 0.0143469 | intron-variant | USP30 | GRCh38.p7 | 12:109081308 | AGCCTAAATCGTTTC[C/T]GGATTTTCTGCAATA | 84749 |
| rs532155001 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088081 | TCATCTTTCTGAATT[C/G]TGCATTGTTACATAA | 84749 |
| rs532240817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109058504 | TTGAACCCGGGAGGC[A/G]GAGGTTGCGGTGAGC | 84749 |
| rs532331232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109057752 | TGCGGAGCAGTACTA[A/G]AACCAAGCCTTGGCA | 84749 |
| rs532375717 | in-del | -/CT | 0.000898145 | 0.0211723 | intron-variant | USP30 | GRCh38.p7 | 12:109057911 | GTTCTCTTCTTCCCC[-/CT]GCTTTTTTTTTAGGG | 84749 |
| rs532447166 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109028635 | GGCGTGTGCCAACAC[A/G]CCTGGCTAATTTTTG | 84749 |
| rs532453917 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109021987 | CACCTCAACCTCCCT[A/G]GTAGCTGGGATCACA | 84749 |
| rs532476614 | in-del | -/ATA | 0.00478085 | 0.0486577 | intron-variant | USP30 | GRCh38.p7 | 12:109074163 | CTTCTTTCATTTAGC[-/ATA]ATATTTCCACGTTTC | 84749 |
| rs532522010 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109058526 | GCGGTGAGCTGAGAT[C/T]GCACCATTGCAGTCC | 84749 |
| rs532659868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109072211 | TTAGTGGTGTAATCA[A/G]CGTAGAAACTTGTAA | 84749 |
| rs532714657 | snp | G/T | | | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022710 | TAGGCTTTCTCTGAG[G/T]GTCTCAAAAGAAACC | 84749 |
| rs532798546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109042731 | CTTCTATTTAACGTA[A/G]TACTGGAAGTTCTAG | 84749 |
| rs532967051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109084764 | TTCCTATTTGGGATT[A/G]AGACAGATTATCCCT | 84749 |
| rs533026067 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109034310 | ATTGATTTCTAATTT[C/T]ATTCCATTGCAGTTA | 84749 |
| rs533028660 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109069426 | AGCTAGGCTGCCACA[A/C]CTCCCCTGGATTGTG | 84749 |
| rs533030814 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109077854 | GTGTGTGAGAGATTA[C/T]GTTATGCAGTTTTAC | 84749 |
| rs533065525 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109070051 | CTAGGAGGCTGCGGG[C/T]GGCATCAGCTTCTAT | 84749 |
| rs533079197 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109049089 | GGCTTAGGATTTTTA[G/T]TTTACATTCTGCTCA | 84749 |
| rs533167027 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | USP30, USP30-AS1 | GRCh38.p7 | 12:109054540 | GTCTCAAAAAAAAAT[A/T]AAAATAAAAATAAGA | 84749 |
| rs533202923 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109040713 | CCTCAGTTCCTTGCC[A/G]CATGGACCTCTCCAT | 84749 |
| rs533323142 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109025841 | TACAAGTGTGCACCA[A/C]CACACCTGGCTAATT | 84749 |
| rs533379105 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109036723 | TTGTTGACAGCTTTG[-/T]TTTTTTTTAATACTT | 84749 |
| rs533553503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109049301 | CGAACATTTAGAGGC[A/G]TGGACTGAAATTCAA | 84749 |
| rs533643338 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109061641 | TCTCGAACTCCTAAG[A/C]TCAAGCAATCTGCCT | 84749 |
| rs533651993 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109064901 | ACAGAAGGGCTGCCC[A/G]AGGGGTATGGGAGAA | 84749 |
| rs533682853 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053799 | TCGCCACTTGTCCCT[C/G]GGTATTTTTTCCTTA | 84749 |
| rs533715958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109059881 | ATCTGCTGACATTCC[A/G]TGGGTATTATACAGA | 84749 |
| rs533797496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109042165 | TTATTGTATTAGCTG[A/G]CCTTCTTTTTTCACT | 84749 |
| rs533827715 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109079910 | TTTGGTAATTTTTTA[-/T]TGTATGCTTAACATC | 84749 |
| rs533830380 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109029109 | AGAAGCTTCTGATTG[A/C]CACAGTACATCTTTT | 84749 |
| rs533887915 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109034686 | TTGTTGATCTTCTGT[C/T]TAGTTGTTCTATCCA | 84749 |
| rs533982586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109068827 | GTGAACACGTCTGTC[C/T]GGTGGCCTTTTTCTC | 84749 |
| rs533989559 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109077463 | GCTAAGACTCCTTGA[A/C]TTGAAGTCTATTTGA | 84749 |
| rs534068288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109069637 | GGAGTTTCCTGCTCT[C/T]TTAGAGCTGGTATTC | 84749 |
| rs534093794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109048542 | GTCAGGAGTTCGAGA[C/T]CAGCCTGGCCAACAT | 84749 |
| rs534164049 | snp | A/C | 0.00159617 | 0.0282053 | utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109047619 | CCCAGCGCTGAGGAC[A/C]AAAGGAAGCAAGCTC | 84749 |
| rs534234935 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109031910 | GGAGTTCGAGACCAG[A/C]CCTGACAACATAGCA | 84749 |
| rs534235335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109040825 | CAATGTATTTTATGA[C/T]CTGGCTTTGGAATTC | 84749 |
| rs534285568 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055717 | AAATATTATTGAGAA[A/C]CTACTATGTGCTAAG | 84749 |
| rs534352642 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | USP30, SVOP | GRCh38.p7 | 12:109021236 | GGTACCAGTGAGCAC[C/T]CTTTGATTGACGATG | 84749 |
| rs534353164 | in-del | -/TG | 0.00119737 | 0.0244387 | downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088087 | TTCTGAATTCTGCAT[-/TG]TTACATAACAAGCCC | 84749 |
| rs534394829 | snp | C/G/T | 2.74616e-05 | 0.00370541 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052766 | GCGGCCGTCAGGTGA[C/G/T]ATTTTGGGGGGCGGG | 84749 |
| rs534469871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109030671 | CGCCAGGCTGGAGTG[C/T]AGTGGCGCTATCTTG | 84749 |
| rs534533565 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109073376 | GCTAGAAAGGAAGAT[G/T]AATGTTGAGCTTGGT | 84749 |
| rs534586971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109067804 | TCAGAGGGGAGATAC[A/G]GCTGTTTTTCACTCA | 84749 |
| rs534683327 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109042614 | ATTGCTTCCAATCCC[C/T]TATTATTAAAAACAA | 84749 |
| rs534763525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109039471 | CATCTGTAAAATGGC[A/G]CTAATTATATCTTAC | 84749 |
| rs534838261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109082240 | AGAATAAACTGTCAC[A/G]CTGAGATGAGAAATG | 84749 |
| rs534842129 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109037266 | AATTTCTACTTCATT[C/T]CTTTTAATAATCTCT | 84749 |
| rs534859727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109031161 | ACTAGATAAACATGT[C/T]CAATGTCTATTTAAA | 84749 |
| rs534964605 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | USP30 | GRCh38.p7 | 12:109067293 | TAATTTTTTTTTTTT[A/T]TTTTTAGTGGAGACG | 84749 |
| rs534979700 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109058924 | TACACCGCTGAGAGG[C/G]GTGTAACTTAGTGCC | 84749 |
| rs535006692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109045231 | TGATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT | 84749 |
| rs535016344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, downstream-variant-500B | USP30, USP30-AS1 | GRCh38.p7 | 12:109051898 | TCACTTTAATGTGGC[C/T]ACTGGAAAATGTAAA | 84749 |
| rs535025963 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109068997 | CCAAAGGCTTGCTTT[G/T]TGCAAATTACCTGAT | 84749 |
| rs535053679 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109045681 | TGAAACAGGGCAGTG[A/C]ATGTAGGTACCTAGC | 84749 |
| rs535384997 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109044650 | TCTAAAAATAAAAAT[A/T]AAAAAAAGAATGATT | 84749 |
| rs535421478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053494 | TCACCCTCCCAAGGG[C/T]TCCAGGCTTCAGAAC | 84749 |
| rs535540025 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109047672 | CTAGGGTCCATCCTC[C/T]GGGCCAGCCCTCTCC | 84749 |
| rs535543744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109070193 | GGAGGCCGCTGCAGT[C/T]ATCTGGCCGAGATGG | 84749 |
| rs535544668 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109082320 | TTCCTTTTAACCTGT[A/G]CTACCTGCCTGACTC | 84749 |
| rs535550170 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109072619 | TTGAATTGATCCTGG[A/G]AAGAACATAATGAGC | 84749 |
| rs535560444 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109033049 | CTAAATCCTATTCTT[A/T]TCAAGACAGTATTCT | 84749 |
| rs535606710 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109031704 | ATAGAAGCTACAATA[C/T]GGATGAGGCTTGAAA | 84749 |
| rs535629908 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109059458 | GCCTCAGCCTCCCAA[A/C]GTGCTGGAATTACAG | 84749 |
| rs535644286 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109066507 | GGCCAACATGGGGGA[A/T]CCCCCATCTCTACTA | 84749 |
| rs535696855 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109067951 | GAAAGAGGCAGGTGA[C/G]TTTACCTTGGAGGCC | 84749 |
| rs535704270 | in-del | -/CACA | | | intron-variant | USP30 | GRCh38.p7 | 12:109081626 | GCACGCATGCGCGCA[-/CACA]CACACACACACACAC | 84749 |
| rs535713905 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109060276 | GGCCATTTTGGTATT[C/G]TGCAGTCATTGGTAA | 84749 |
| rs535748784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052615 | GGAACCGTCGTATCC[C/T]TCGGTCCGGCGGCGG | 84749 |
| rs535790295 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109060925 | TGTTGGGATTACAGG[A/C]GTGAGCTACCATGCT | 84749 |
| rs535831394 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046460 | CTTCAATTAATTGGA[A/T]GAGGCCCACCCACTA | 84749 |
| rs535877611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109039602 | AACTATTCTTATTAC[C/T]AAGTGATAAGAATCC | 84749 |
| rs535918009 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109066152 | AGCTGCTCAGGAGGC[A/C]AAGATGGGAGGATTG | 84749 |
| rs535978654 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109031237 | ACATAAAACAACAAC[C/G]CATTTACAAATGCTA | 84749 |
| rs535981221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109058954 | CACTTTTCTGGAAAG[C/T]AGTTTGGAACTACAC | 84749 |
| rs536017972 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109030617 | AAAGGTAGGTTGCTT[A/G]TTTGTTTGTTTGTTT | 84749 |
| rs536084036 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109045815 | CAGAATCAATAGAAC[A/G]CGTGTGTATGTGTGT | 84749 |
| rs536165806 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109049677 | AAAATTAGCCAGGCA[C/T]GGTGGCGCGTGCCTG | 84749 |
| rs536270567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109081454 | TTCAATCTGAAAGGG[C/T]TTTGAGGCATTTTAT | 84749 |
| rs536300274 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109073235 | ACAGAAACCGTATAT[A/G]AAGATAGATCTGTGT | 84749 |
| rs536349174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109050825 | GCCTGACCAACATGG[C/T]GAAACCCCGTCTCTA | 84749 |
| rs536435426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109051216 | CATATTGGGTCAAGG[A/G]AAAAATATGGTTAAA | 84749 |
| rs536436993 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109024795 | GGGCTAATTTTTTGT[A/G]TTTTTAGTATTGACA | 84749 |
| rs536539439 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088141 | TCCCTGTTGGTAAGG[C/G]AAATGCCAGCTCCCT | 84749 |
| rs536625756 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109064894 | GGAGCTAACAGAAGG[A/G]CTGCCCGAGGGGTAT | 84749 |
| rs536693979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109024625 | ACTGGTAAAGCAGCA[C/T]TTTTTTTTTCCCGAG | 84749 |
| rs536707050 | snp | C/T | 0.000214311 | 0.0103494 | missense, intron-variant | USP30 | GRCh38.p7 | 12:109058061 | GGGATCAGAAGGAGC[C/T]CCCCTCACACCAGTA | 84749 |
| rs536719463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109059671 | GCTGCATGCCACCAC[A/G]CCCGGCTAATGTTTG | 84749 |
| rs536730180 | in-del | -/GTT | | | intron-variant | USP30 | GRCh38.p7 | 12:109056202 | GTTGTTGTTGTTGTT[-/GTT]TTTTATGAGACTGAG | 84749 |
| rs536793359 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109035517 | TACAGGCATGTGCCA[C/T]CATGCCCAGCTAATT | 84749 |
| rs536888128 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109028273 | CATTTTTGTATTGCT[C/G]TAAAGGAATACCTGA | 84749 |
| rs536953504 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109023761 | CCTCGGCCTCCCAAG[C/T]ACCTGGGATTACAGG | 84749 |
| rs536992823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109071545 | AGGGTGTCTGCCCGA[A/G]GTGGGTAGTTCTGAT | 84749 |
| rs537045435 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109043760 | AAAACTTTTGCGCAT[C/G]AAAAGACACTATCAA | 84749 |
| rs537128109 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109049141 | CCTTCAGGAAATTTT[C/T]CTTTGAATTCACAAC | 84749 |
| rs537216159 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109082449 | AGAGCATCAGTGTTC[A/G]CTCTTCACATTCTCT | 84749 |
| rs537236012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109045652 | GAACCCACTAGGAGG[A/G]GCTGTTGGGAGGATG | 84749 |
| rs537268699 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109080904 | AGTAGGCTGCACCAT[C/G/T]TAGGTTCTTGTAAGC | 84749 |
| rs537285266 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109038621 | TTCCCTTTCTCTTGG[A/C]TAAATAAATACCTAG | 84749 |
| rs537303014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109081577 | TGAATCGTTTTTCTT[C/T]TGCTCCAGAAATTTT | 84749 |
| rs537371401 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109030517 | ATTCTGGAGATCTAA[A/C]GTACAGCATGGTGAC | 84749 |
| rs537393985 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109025138 | TCAGAACTGCAGGCT[C/T]TTTAGTCTTTAGAAA | 84749 |
| rs537423225 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109050841 | GAAACCCCGTCTCTA[C/T]TAAAAATACAAAAAA | 84749 |
| rs537438790 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109043109 | TTAAAGAAGACATAA[A/T]GGAAACACATCCCAA | 84749 |
| rs537596629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109079644 | GTGTTGGGATTACAG[A/G]TGTGAGCCACCATAC | 84749 |
| rs537599270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109029021 | TTGTTGTGGTCCTTA[C/T]CCAATTACAGGGCAT | 84749 |
| rs537627809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109056046 | AACAGCAGTGCAAAC[A/G]CCTTGAGGTCAGAGC | 84749 |
| rs537713946 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109056887 | GAGGTTGGTCATATT[A/T]GTTCTCTGTATCTTT | 84749 |
| rs537714071 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109049366 | AAGAGTGAGAGAGAG[C/G]GGGGAACAGCCAGTC | 84749 |
| rs537732898 | snp | A/G | | | utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109024835 | CATGTTAGCCAGGAT[A/G]GTCTCGATCTCCTGA | 84749 |
| rs537795944 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109026428 | GCCAGGTCAGTTGCC[A/T]TAACAAAATATCATA | 84749 |
| rs537810579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109026713 | ATTCAAGCCATCCAC[C/T]CACCTCGGCCTCCCA | 84749 |
| rs537873629 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109073783 | CCAGTGGTTGAGTCT[A/G]TGCTCATGGTGGACA | 84749 |
| rs537883668 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP30 | GRCh38.p7 | 12:109075334 | TTCTCTCCACACCCT[C/T]GGCAACACTTGTTAC | 84749 |
| rs537907220 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109086626 | TTGTTGCTTTTATCT[G/T]TTGTATATTGGACTG | 84749 |
| rs537952454 | snp | A/T | | | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109087079 | TTCTGAATTTATTCA[A/T]TTCCAATAGCCTAAT | 84749 |
| rs537995617 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109063392 | AGGCGTGAGCCACCA[C/T]GCCAGGCCTAGGCTG | 84749 |
| rs538090542 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109041550 | TGAGGCAGAGGAATC[A/G]CTTGAACCTGGTAGG | 84749 |
| rs538150867 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109042292 | GAATAAATATTGCAT[G/T]GAGATGGTACAAAAT | 84749 |
| rs538200165 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109036518 | GGCCTGGCAGGTCTC[A/C]AACTCCAGACCTGAG | 84749 |
| rs538254388 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109069776 | GCAGAGGAGGAGGAG[C/G]CAAGCTACAGGGGGA | 84749 |
| rs538291378 | in-del | -/AAGAG | 0.00298263 | 0.0385022 | downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088173 | TAGAGTCGAGAGGGA[-/AAGAG]AAGAGAAAAGAGAAA | 84749 |
| rs538298789 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109029139 | TTAAGCCAGTTTATA[G/T]AGATCATGGAGAGTT | 84749 |
| rs538308102 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109071780 | TATAGGGGAGGCAAG[C/T]GTAATCTTTGTACAA | 84749 |
| rs538391957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109072578 | GGCTTATTTGTACTT[C/T]AAACAAGGGCTTTCT | 84749 |
| rs538407652 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109048291 | GGTTTCACCATGTTG[-/C]CCAGACTCGTCTCAG | 84749 |
| rs538432226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109048417 | GGTTTTAAATATTTC[C/T]GTTTCCATCAGTGAT | 84749 |
| rs538452243 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109050005 | AGTGCAATAAAACAA[A/G]ATATGCCGGGCGGGG | 84749 |
| rs538587093 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054244 | ACCTTTCACCAGCTG[A/G]GCATGGTGGCTCACA | 84749 |
| rs538589090 | snp | G/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109087040 | AGCTGGCATCTAGTA[G/T]TGTCATGTTGCTCTA | 84749 |
| rs538706190 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109029771 | TGCTCCTACTCTGTC[A/C]GACAGGGCATATGGC | 84749 |
| rs538757846 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, missense | USP30 | GRCh38.p7 | 12:109083147 | CTTCTGGGTCCCTTA[A/T]GACAGGAGCACAAGG | 84749 |
| rs538833844 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | USP30 | GRCh38.p7 | 12:109067368 | GTAATCTGCCCACTT[C/T]GGCCTCCCAAAATTC | 84749 |
| rs538859815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109050775 | ACACTTTGGGAGCCC[A/G]AGGCGGATGGATCAC | 84749 |
| rs538919968 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109086006 | AAAACTGTACTGTTG[C/T]GTGTGCAAGCGGCCC | 84749 |
| rs538920386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109078213 | AGTGGATCACGAGGT[C/T]AGGAGTTCAAGACCA | 84749 |
| rs539009943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109063405 | CACGCCAGGCCTAGG[C/T]TGAATAATATTCTGT | 84749 |
| rs539057296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055047 | AAACACGTATGTATG[C/T]ATGTGTAACATATAT | 84749 |
| rs539059812 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109085417 | GTACATCACACATAC[A/T]TATAGTGTACATAAA | 84749 |
| rs539105406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109064164 | GGCATGAGCCACCAC[A/G]CTCAGCATTGTTTGG | 84749 |
| rs539145979 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109049901 | TGAGCACATGCTGTT[C/G]AAAATGGTGCCAATA | 84749 |
| rs539179919 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109033869 | GTCACATAGCTCATC[A/C]CTCCATGAAAATACA | 84749 |
| rs539232524 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109068699 | TTTTTAAGGTCCGAC[G/T]TCTCCATCAAGGACT | 84749 |
| rs539256135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109077623 | TTTTAGTTGGAATGC[C/T]TAGTCCATTTACATT | 84749 |
| rs539262136 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109026878 | AGATGGCCACCTTCT[C/G]TCTGTGCTTACATGC | 84749 |
| rs539268495 | in-del | -/TATAA | 0.00318978 | 0.0398085 | intron-variant | USP30 | GRCh38.p7 | 12:109066334 | TGGTCTAGAAGTAAT[-/TATAA]TATAAATAAGCCCAT | 84749 |
| rs539361758 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109062559 | GGTCTCAATCTCCTG[A/C]CCTCGTGATCCGCCC | 84749 |
| rs539511163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109083594 | GGAGGCTCCACGGGG[C/T]TGAATGATTGGTCCA | 84749 |
| rs539524275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109066935 | AACAAATTTATATTG[A/G]TGATGATAGTTTGAA | 84749 |
| rs539531552 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109062984 | TGTACCTCATTAAGC[A/G]GACTCATATAATATT | 84749 |
| rs539557299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109041612 | TGCACTCCAGCCTGG[A/G]TGACAGAGCGAAACT | 84749 |
| rs539593578 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109076435 | TTTTTCTTTGCCTTA[C/T]TATCCTGGCTAAGAC | 84749 |
| rs539602358 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109026063 | CTACCATGATTCTTT[A/T]AAATAATTTTTTAAT | 84749 |
| rs539688199 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | USP30 | GRCh38.p7 | 12:109061931 | ATTGTAGGTTTTTTT[G/T]TTTTCTGTTTTGTTT | 84749 |
| rs539750719 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046959 | GCCTGGGCCTCCCAA[A/C]GTGGTGGGATTACAG | 84749 |
| rs539762659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109039668 | CAGGCTGTAGTTCAG[C/T]GGCACGATCTCAGCT | 84749 |
| rs539806898 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109084237 | TGTCTAAAACACACA[A/C]AAAAAATGTCATCAG | 84749 |
| rs539807149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109063186 | CTCACTGCCACTTCC[A/G]CCTTCCAGATTCAAG | 84749 |
| rs539853628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109031847 | GATTACTCGGGCTTG[C/T]AATCCTAGCACTTTG | 84749 |
| rs539945543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109077817 | GCTTTACTCTTGTGT[A/G]TTTGTGTTGGGGGGG | 84749 |
| rs539959582 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109025631 | ATTTGCCTGTAGATA[A/C]TAAAAGAAGCAGCTA | 84749 |
| rs539966151 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109026981 | TCATGTCAGCCCCAC[A/C]TGCATGACCTTCTGT | 84749 |
| rs539979537 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109069951 | ATAAAGCTGCCACCT[A/G]TGGAGAATGGCAGGG | 84749 |
| rs539981242 | in-del | -/CT | | | intron-variant | USP30 | GRCh38.p7 | 12:109029479 | CTACAGGCATATCCC[-/CT]GAGTGTGCATTTAGC | 84749 |
| rs540028867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054327 | GGAGTTCGAGACCAG[C/T]CTGGGCAATGTAGTG | 84749 |
| rs540215316 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109025714 | TCTTGCTCTGTCACC[C/T]AGGCTGGAGTGCAGT | 84749 |
| rs540224365 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109076985 | GATCCGCCTGCCTCA[G/T]CCTCTCAAAGTGCTG | 84749 |
| rs540245131 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109060715 | GCTGGAATGCAGTGG[C/T]GGGATCTCGGCTCAC | 84749 |
| rs540247005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109068186 | GCTGTTACCAACAGC[A/G]AGTCTGAAGCAGAGG | 84749 |
| rs540254650 | in-del | -/A | 0.0126979 | 0.078662 | intron-variant | USP30 | GRCh38.p7 | 12:109072406 | CTTTTAAGATATGAT[-/A]ATAATTTGCTTGTTT | 84749 |
| rs540348990 | in-del | -/AGCTACTCGCG | 0.0138799 | 0.0821421 | intron-variant | USP30 | GRCh38.p7 | 12:109044522 | CGTGTCTGTAGTCCT[-/AGCTACTCGCG]AGGCTAGGGTGGAAG | 84749 |
| rs540439390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109082074 | TGTGTGCTGATGTAG[C/T]GCCTCTCACACCAGT | 84749 |
| rs540489053 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | USP30 | GRCh38.p7 | 12:109057074 | GTTCTCATTAGTACG[A/G]CAATTGTAGTTTTCA | 84749 |
| rs540525813 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | USP30 | GRCh38.p7 | 12:109082301 | TCCCATTTGTTTTAC[A/G]CCCTTCCTTTTAACC | 84749 |
| rs540727955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109039111 | TTTGATTAGATCCAA[C/T]GTATCAGTTTTTTCT | 84749 |
| rs540930578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109050868 | AAAAATTAGCCGGGC[A/G]TGGTGGTGTGCACCT | 84749 |
| rs541070839 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109080216 | TCTTCCTGGCATTTC[A/C]CCTGGTCTCTCCACC | 84749 |
| rs541096591 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046013 | GCTGGAGACCTATGG[A/G]AAAAGCCAGTGTTGC | 84749 |
| rs541098056 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109026467 | GCTTACACAACAGAA[-/T]TTTTTTTTTTTTTTG | 84749 |
| rs541170472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109023556 | CGAAACTCTGTCTCA[A/G]TAAATAAATAAATAA | 84749 |
| rs541180930 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022745 | ATTGCGGGTATAGTA[A/G]GAGAAATTGGAACTA | 84749 |
| rs541190521 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109039902 | GCGTGAACCACCACA[C/T]CTGGCCAGCCATTTT | 84749 |
| rs541243479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109066475 | CGATCATGAGGTTAG[A/G]AGTTCGAGACCAGCG | 84749 |
| rs541252058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109050563 | TACTCAGTCTGGAGT[C/T]GGAGAAAGCGATTGA | 84749 |
| rs541340199 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109030760 | AACTGGGATTACAGA[C/T]ACCTGCCACCACGCC | 84749 |
| rs541375581 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109059719 | GTGTTCGCCATGTTA[A/G]CCAGACATGTCTCGA | 84749 |
| rs541526205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109047186 | TTTTTTTTTTTAACC[A/G]AGGAAACCCTTCTTA | 84749 |
| rs541569182 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109040317 | ACTGCTATGTTCTGA[A/T]CCACTTGACTGTGTT | 84749 |
| rs541601073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109058339 | ACTTTAGGAGGCCAA[A/G]GCAGGTGGATCACGA | 84749 |
| rs541856624 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109038883 | TTGACCATCTTTTCA[C/T]GTGCCTACTGATCAT | 84749 |
| rs541860823 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109072947 | AGGTCAGGTAGTGAA[A/T]AAGAAGCACAGCCAG | 84749 |
| rs541880120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109039797 | TGCATTTTTGGTAGA[A/G]ATGTGGTTTCACCAT | 84749 |
| rs541943823 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109082590 | GTGCCGCTATAACAC[C/G]ACTGTGGTCTGCAGC | 84749 |
| rs541981019 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109074724 | GTGTGTGTGTGTGCA[C/G/T]GTGCACCTGTGCTCA | 84749 |
| rs541982725 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, missense | USP30 | GRCh38.p7 | 12:109083158 | CTTATGACAGGAGCA[C/G]AAGGCTTGTACAATG | 84749 |
| rs541996333 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, downstream-variant-500B | USP30, USP30-AS1 | GRCh38.p7 | 12:109051580 | CTGACCTCTTTTTTT[G/T]TTTTTTTGAGATGGA | 84749 |
| rs542029105 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | ALKBH2, USP30 | GRCh38.p7 | 12:109087688 | ATCTACCATCAAAGA[A/T]AGATAGAGAAAAGGG | 84749 |
| rs542041825 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109031824 | AACAGAAGGTAGAGA[C/T]GAGGTGTGATTACTC | 84749 |
| rs542042501 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109044693 | TTTATGTTATATGTA[A/C]TTTGCCACAATAAAA | 84749 |
| rs542062461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109059893 | TCCATGGGTATTATA[C/T]AGAGTGCAATGTATG | 84749 |
| rs542101521 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB, nc-transcript-variant | USP30, USP30-AS1 | GRCh38.p7 | 12:109052492 | AAAGGACGTGGTCCG[A/T]CAGCTATTGCTCTCC | 84749 |
| rs542101526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109060573 | CGCTGCCAGCGTTCA[C/T]CTAATTTTACGTAAA | 84749 |
| rs542159521 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109059064 | AACGTAGATTGTGAC[-/T]TTAACTAGCCTGAAA | 84749 |
| rs542185451 | snp | A/G | 0.000479042 | 0.015469 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052789 | GGGGCGGGGCTGCCG[A/G]AGAGGCCGGGACCAG | 84749 |
| rs542232385 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109065235 | GTATTTTTTTCTCTC[A/G]CACTCTAGCAGTACT | 84749 |
| rs542243816 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109030004 | GCAAATAGTTTATTT[A/C]CAGTAATCATTATTG | 84749 |
| rs542298313 | snp | A/G | 3.29924e-05 | 0.00406142 | missense | USP30 | GRCh38.p7 | 12:109073486 | CTCAACATCCTTTTC[A/G]TGGAAGACTCACTAG | 84749 |
| rs542412380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109035822 | AATTTATAATTATTG[C/T]TTTATGTGGTTGTCT | 84749 |
| rs542414008 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109027937 | TTGCTGAGTCATATG[G/T]TAACTATGTTTAAGT | 84749 |
| rs542448692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109028546 | GCAATGGTGTGGTCT[C/T]AGCTCACTGCAACCT | 84749 |
| rs542481972 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109045272 | GCGTGAGCCACTGCG[C/T]CCGCCCAAACATCTT | 84749 |
| rs542508561 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109025531 | TATTGGGAAAAACTA[A/T]ATCCTCCTCAAGTTT | 84749 |
| rs542550543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109071340 | GTGGAGGTCAAGGCT[A/G]TCTCAGTGAAACAGA | 84749 |
| rs542569838 | snp | C/G | 0 | 0 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022388 | TGACAAAGGGTGGGG[C/G]AAGTTGGAAGAGGGA | 84749 |
| rs542632504 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109049547 | GGACCAGGCACGGTG[A/G]CTCACGCCTGTAATC | 84749 |
| rs542641383 | in-del | -/TTGTTG | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109056175 | GATTTGACTTAGTTT[-/TTGTTG]TTGTTGTTGTTGTTG | 84749 |
| rs542689867 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109044214 | CTAGGAACTGAGGAG[C/T]GTGTAGAATGAGGAG | 84749 |
| rs542728303 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109042625 | TCCCTTATTATTAAA[A/C]ACAATGTTACAGAAC | 84749 |
| rs542806627 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109086139 | GTGTGTAGGTGGTTC[A/T]GTTGTGTTAAGAAAG | 84749 |
| rs542871437 | snp | A/G | 1.64768e-05 | 0.00287021 | missense | USP30 | GRCh38.p7 | 12:109081385 | CTAAGTATTCCAGCC[A/G]CCACATGGGTATGTA | 84749 |
| rs542938501 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109072009 | AGGAATGCTAAGTGA[C/G]CCCTCATTTCCCTGT | 84749 |
| rs543025900 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109078239 | GACCAGCATGGCCAA[C/T]ATGGTGAAACCCCGT | 84749 |
| rs543118434 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109043512 | AATAGTTCTGGGAAA[A/C]CTGGATATCTATGTG | 84749 |
| rs543209646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109029467 | ATCTCTCTGACACTA[C/T]AGGCATATCCCCTGA | 84749 |
| rs543246773 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022465 | ATAAAAGGACTTGAA[A/T]ATCCAAAATTGAATG | 84749 |
| rs543295979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055600 | AGACAGGGTTTCACC[A/G]TGTTGGCCAGGCTGG | 84749 |
| rs543333812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109023390 | AAACCTCGTCTCCAC[C/T]TGAAAATAAAAAAAC | 84749 |
| rs543347864 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109040607 | GCTATGGCTGTGGTC[C/T]CATCTGAAGACTTGA | 84749 |
| rs543383403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109056359 | CACCACGGCCAGCTA[A/G]TTTTTGTGTTTTTAG | 84749 |
| rs543398789 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109058486 | CTGAGGCAGAAGAAT[C/T]GCTTGAACCCGGGAG | 84749 |
| rs543582071 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109036307 | GTATTTCTTTCTTTC[-/T]TTTTTTTTTTTTTTA | 84749 |
| rs543661884 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109072154 | CCAGATAGGCTAATT[A/G]AGGCTACCTTTAGAA | 84749 |
| rs543699247 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109074222 | TTTGTTCCTTTTATT[A/C]CCAAATAATATTGCA | 84749 |
| rs543702005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109072778 | TGTAGTAATAGGAAC[A/G]AATATTTTTTGAGCC | 84749 |
| rs543709348 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109043122 | AATGGAAACACATCC[C/G]AAGTCCATGGATTGG | 84749 |
| rs543744060 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109066360 | TAAGCCCATCAAACT[A/T]TTATTAGGCCTGATT | 84749 |
| rs543867141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109044514 | CAAAGGCTCGTGTCT[A/G]TAGTCCTAGCTACTC | 84749 |
| rs543937429 | snp | A/T | | | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109087683 | CTGAAATCTACCATC[A/T]AAGAAAGATAGAGAA | 84749 |
| rs543979718 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109064426 | TGCACCCATCACCCC[A/C]GGCTAATTTTTGGGT | 84749 |
| rs544012837 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109056467 | CAAAGTGCTGGGATT[A/G]CAGGGATGAGCCACC | 84749 |
| rs544100232 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109084759 | CACTTTTCCTATTTG[G/T]GATTAAGACAGATTA | 84749 |
| rs544126757 | snp | C/T | | | utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109027476 | GTAGAGACAGAGTCT[C/T]GCTATGTAACCCAGG | 84749 |
| rs544148865 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109041721 | ATGATGCCTATTCCA[C/T]GGCAAATTATTTTTT | 84749 |
| rs544170272 | in-del | -/C | | | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109021725 | GGCACATAGAAGGTA[-/C]CCCCATAAATATTTG | 84749 |
| rs544185724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109034212 | TAATTTCCCTTGTTA[A/G]TGTTTCTCTTACCTA | 84749 |
| rs544191498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109034836 | ATTACAATTGTTTTA[C/T]CTTCTTAATGAATTG | 84749 |
| rs544215815 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP30 | GRCh38.p7 | 12:109070038 | GATTGTGCAGGGACT[A/G]GGAGGCTGCGGGCGG | 84749 |
| rs544342382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109048013 | TCACCAGTGTATCTC[A/G]GAGTTTTCCAGAGGC | 84749 |
| rs544397072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109032009 | TGGGAGACTAAGGTA[A/G]GAGGATCACTTGAGC | 84749 |
| rs544473970 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109064086 | ACCATGTTGGCCAGG[A/G]TGGTCTCGATCTCTT | 84749 |
| rs544510840 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109048060 | TGATCATGGGTCTGA[C/T]GTCTAATAGAATGCC | 84749 |
| rs544528614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109026299 | CAGGCTGGTCTCGAA[C/T]TCCTGGGCTCAAGTG | 84749 |
| rs544582315 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP30 | GRCh38.p7 | 12:109034118 | CAACGTGTCTGAGTC[A/G]TTGTTTTCAAAGGAA | 84749 |
| rs544586936 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052823 | CCCCAGCTTGGGCCC[C/G]TGACGGCTTTTTCAT | 84749 |
| rs544607056 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109068943 | GATTGTCAACCCATT[G/T]TCTTTGTCTAAAGCT | 84749 |
| rs544626921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109071251 | GCCACAGAATCATTC[A/G]TGTTAAGATGATAAA | 84749 |
| rs544687337 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109050283 | TGGGCCACAGAGCGA[G/T]CCTCCATCTCAAAAA | 84749 |
| rs544749820 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109058955 | ACTTTTCTGGAAAGC[A/G]GTTTGGAACTACACA | 84749 |
| rs544826437 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109057513 | GAACAGAATCATTGT[C/T]CTGGGGAAGTAACAA | 84749 |
| rs544848283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109068278 | TCCACAGCCACACTT[C/T]CAAGATGGCCTTGTC | 84749 |
| rs544881569 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109085558 | GCATTTGGTGGTATG[G/T]ACTTACCATTGTATT | 84749 |
| rs544901470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109034944 | GTAATTACTTCAGCT[C/T]GCTTTTGGTTGCTGT | 84749 |
| rs544934495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109061558 | GGACTACAGGCACAT[A/G]CCACCAGGCCTGGCT | 84749 |
| rs544936938 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109070515 | CATTGTGAATGTTGG[C/G]GGCTTTGTAGGCCAG | 84749 |
| rs544989032 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109027753 | GACTGAATAATATTT[A/C]TTTGTAGGTATATGG | 84749 |
| rs545059535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055524 | TCTGCCTCGGCCTCC[A/G]GAGTAGCTGGGATTA | 84749 |
| rs545066128 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109021397 | TAATAGGCACTGGGG[G/T]TATGACAGAACAAAT | 84749 |
| rs545101588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109041774 | CTTGAAGAGCTACTT[C/T]GGAAGGTCGAACTGT | 84749 |
| rs545178467 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109034321 | ATTTCATTCCATTGC[A/C]GTTAGAGAACATATT | 84749 |
| rs545227325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109026344 | GCCTCCCAAAGTGCT[A/G]GGATACAGTTGTGAG | 84749 |
| rs545233213 | in-del | -/G | 0.00674803 | 0.057693 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052646 | GGCGGCGGTAGCGGA[-/G]GGAGACGGTTTCAGG | 84749 |
| rs545359844 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109034506 | CTGAGGTGGGAGGAT[C/T]GCTTGAGCTCATGAG | 84749 |
| rs545426767 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109062818 | CATCCCTCTCTAGAA[C/G]TCTTCATCATCCCGT | 84749 |
| rs545473389 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109079873 | GTGAGGTCCTCGTGT[A/G]CTGACTTCTTTGTAT | 84749 |
| rs545491036 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP30 | GRCh38.p7 | 12:109029784 | TCAGACAGGGCATAT[A/G]GCAGTCCATAACAGA | 84749 |
| rs545577645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109083981 | GGCCCTGGTTTTAAA[C/T]CAAAGACCTCTGCAC | 84749 |
| rs545596219 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109032936 | AGTGAATACTTTAAG[A/G]GAGACTGGAATAGAG | 84749 |
| rs545642826 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | USP30 | GRCh38.p7 | 12:109062357 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 84749 |
| rs545661706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109061214 | TGGGTTAAAAACACC[A/G]CTCCAAAGATTTTGT | 84749 |
| rs545678864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109069845 | GTTTCAGCGGAGACC[A/G]GAAGTATAAAAGAGA | 84749 |
| rs545730745 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | USP30, USP30-AS1 | GRCh38.p7 | 12:109054544 | CAAAAAAAAATAAAA[A/T]TAAAAATAAGAAAAA | 84749 |
| rs545811440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109074458 | ACTGCCAGACTGTTT[C/T]CCAAAGTGGCTATGC | 84749 |
| rs545833452 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109031403 | TTCCAATTCAGCTGT[A/T]TGAGGTATAGCACTT | 84749 |
| rs545843927 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109041024 | CCAGGAAATGGGGTG[A/T]CTGGTTCCAGTTCTG | 84749 |
| rs545900918 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109066942 | TTATATTGATGATGA[C/T]AGTTTGAAGATACAG | 84749 |
| rs545911221 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109075804 | TGCAAAGTGTCTGTT[C/T]AGCTCCTTTGCCCAT | 84749 |
| rs545954364 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | USP30 | GRCh38.p7 | 12:109076873 | AGTAGCTGGGACTAC[A/G]GGCGCCCGCCACCAC | 84749 |
| rs545971592 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109084314 | AAAAGACATGTAAAT[A/G]TGGCCTTAATTATGT | 84749 |
| rs546072837 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109038249 | TGTTCTCACCATGCA[A/G]CTCCCAATTGTAAGC | 84749 |
| rs546172236 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109024479 | CCCAGGCTGGCCTCA[A/C]ACTCGTGAGCTCAAG | 84749 |
| rs546211959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109082474 | TTCTCTTCCCTCCAC[C/T]GTTTCTGTTATTTAA | 84749 |
| rs546242140 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109075987 | CATATGTTGCCTTTT[C/G]ATTTTGTTGATTGTT | 84749 |
| rs546261827 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109025082 | GGAAAGGTGAGTTGA[A/T]CTCTTTCTCCAGGAG | 84749 |
| rs546283190 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109068442 | GCACCCCTTATTTTT[A/C]AAGGTGTTCTCTTGT | 84749 |
| rs546384912 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109025284 | TGTTGGCCAATTCCC[C/T]TGATAAATCCCTTCA | 84749 |
| rs546414810 | snp | A/G | | | intron-variant, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053767 | TGTCATTTTGCAGAG[A/G]AATGGAGTTTCCAAA | 84749 |
| rs546439569 | snp | A/T | | | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109085988 | ACTGTCCAGGAAAAA[A/T]GTAAAACTGTACTGT | 84749 |
| rs546494082 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109030858 | TGACCTCATGATCCA[C/T]CTGCCTCGGCCTCCC | 84749 |
| rs546508725 | snp | C/T | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | USP30, USP30-AS1 | GRCh38.p7 | 12:109051773 | TGGGGTTTCACCATG[C/T]TGGCCAAGCTGGTCT | 84749 |
| rs546523541 | snp | A/G | | | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022735 | GAAACCATCCATTGC[A/G]GGTATAGTAGGAGAA | 84749 |
| rs546663757 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109023750 | GCAATTCTCTGCCTC[A/G]GCCTCCCAAGTACCT | 84749 |
| rs546702752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054184 | ACTTTTGTGAACTCA[C/T]GTATCGTGTAAAAGC | 84749 |
| rs546711672 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109061735 | TTTTTAATTATACAA[A/G]TAATGCATGAATCAG | 84749 |
| rs546731129 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052898 | TTCTGCGTCCTTTAG[A/G]GTTGGAGGCCTGGGC | 84749 |
| rs546747897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109062459 | CCTGCCTCAGCCCCC[C/T]GAGTAGCTGGGATTA | 84749 |
| rs546796434 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109066624 | CAGGAGGCGGAGGTT[A/G]CAGTGAGCTGAGATC | 84749 |
| rs546803046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109039898 | ACAGGCGTGAACCAC[C/T]ACACCTGGCCAGCCA | 84749 |
| rs546818389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046887 | TTTTTAGTAGAGACG[A/G]GGTTTCACCATGTTG | 84749 |
| rs546876478 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109067176 | TGGAGTGCAGTGGCA[C/T]GATGTCTGCTCACTG | 84749 |
| rs546876536 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | USP30 | GRCh38.p7 | 12:109066947 | TTGATGATGATAGTT[G/T]GAAGATACAGGAATC | 84749 |
| rs546882242 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109059387 | TTTTAGTTGAGACAG[A/G]GTCTTACTATGTTGG | 84749 |
| rs546884044 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109073817 | TAGATTCTAGGGCTG[G/T]TTTTTTCCCCTTTAC | 84749 |
| rs546904584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109024549 | AGGCTTGAGCCACCG[C/T]GCCCGGCCACAATGA | 84749 |
| rs546915107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109060181 | TTTAAAGAGCAGCGT[A/G]CAAAATATAATTTGA | 84749 |
| rs546927969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109032245 | GGAGGCAGAGGTTGC[A/G]GTGAGCCAAGATCAT | 84749 |
| rs546976351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109045444 | GGTGCAGATCACAGT[A/G]GGGGTGGGGGGTGAT | 84749 |
| rs546976413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109037478 | TTTTTTTGTTTCTTC[A/G]CATGTGTCATTATTT | 84749 |
| rs546987462 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052588 | ACTGCGGCCGCAGGT[A/T]CCGCTGTCTCGGGAA | 84749 |
| rs547024068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046395 | TGGGATTACGGGCGT[A/G]AGCCATTGCACCCAG | 84749 |
| rs547062972 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109038352 | ATTCATTTTTATGGT[G/T]GCATAGTATTCCATG | 84749 |
| rs547074420 | in-del | -/TTG | 0.00518131 | 0.0506341 | intron-variant | USP30 | GRCh38.p7 | 12:109056178 | TTGACTTAGTTTTTG[-/TTG]TTGTTGTTGTTGTTG | 84749 |
| rs547114952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109080599 | TTCTTCTACATTTTG[C/T]TTAACATAGTGTTTC | 84749 |
| rs547158219 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109037221 | CGCTAGTGAATTTTT[C/T]ATTTCAGTTATTCTA | 84749 |
| rs547162837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109039530 | AATATAAGGAGATGA[C/T]ACAGAAGCCAGCATT | 84749 |
| rs547288755 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109050776 | CACTTTGGGAGCCCG[A/T]GGCGGATGGATCACG | 84749 |
| rs547336187 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109044880 | CCATATACCATCATC[A/T]TTATGTTATCACACT | 84749 |
| rs547354730 | in-del | -/CTTTTTTTTTTTTT | | | intron-variant | USP30 | GRCh38.p7 | 12:109079351 | TTTCTTTTTTTTTTT[-/CTTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 84749 |
| rs547370286 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088107 | CATAACAAGCCCTAC[A/G]CTTTAAACCTTTCTG | 84749 |
| rs547479442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109030322 | TATTGTGTGGATTAA[A/G]CAAGATGATGGATAT | 84749 |
| rs547582448 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109058559 | CCTGAGCAACAAGAG[A/C]GAAACTCCGTCTCAA | 84749 |
| rs547736932 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109079496 | AGCCCCCTGAGCAGC[G/T]GGGACTACAGGTGTG | 84749 |
| rs547753770 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109078733 | TTTGGCCTAAAAACT[G/T]CCTTTTAACATTTGT | 84749 |
| rs547767035 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109030438 | AGTTTTTGAAAGAAA[G/T]GGGATATAGGGAGAT | 84749 |
| rs547813812 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109071525 | ATTCTACCCACATTC[A/T]CTGTAGGGTGTCTGC | 84749 |
| rs547842123 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109065240 | TTTTTCTCTCACACT[C/T]TAGCAGTACTGGTCT | 84749 |
| rs547850970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109024106 | GTTGTCTAACTTTCC[A/G]TGCTTGCATTTCCTC | 84749 |
| rs547888118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109073260 | CTGTGTAAATTCTCC[C/T]ATGAAGGAATGGGAT | 84749 |
| rs547899462 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109064850 | TAAAGGAGGCATTAA[A/C]ATTTTCCTTTGGGGG | 84749 |
| rs547929794 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109062520 | TTTTTAGTAGAGACG[A/G]GGTTTCACCGTGTTA | 84749 |
| rs547939450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109065563 | ACAAAAACGGAGGTA[C/T]TGAACAGAATTATAA | 84749 |
| rs547985607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109042755 | GTTCTAGCCACAGCA[A/G]TTAGGCAAGAAAAAG | 84749 |
| rs548104083 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP30 | GRCh38.p7 | 12:109044990 | TAAGGTCAAACATCT[C/T]TTTTTTTTTTTTTTT | 84749 |
| rs548108975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109036216 | ATGTAGCCAACTTTA[C/T]GGATGCTCTTTATTT | 84749 |
| rs548183392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109081509 | CAGATACATGGTTGG[C/T]TGAACCCTCTCTTAA | 84749 |
| rs548211836 | in-del | -/TGGTCC | | | intron-variant | USP30 | GRCh38.p7 | 12:109029011 | AATGTTGGCTTGTTG[-/TGGTCC]TGGTCCTTACCCAAT | 84749 |
| rs548265384 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109074083 | TACCTCTGTCTCTAT[G/T]GATTTGCATATTCTG | 84749 |
| rs548298575 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109067238 | CCTGCCTCAGCCTCC[C/T]GAGTACCTGGGACTA | 84749 |
| rs548384831 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109079535 | CACCCAGCTAATTTT[G/T]TTTTATTTTTTGTAG | 84749 |
| rs548397407 | in-del | -/TGT | 0.000336346 | 0.0129638 | intron-variant | USP30 | GRCh38.p7 | 12:109082789 | GTTTTGAGGACTCCG[-/TGT]TGTATCCTGCCCCTG | 84749 |
| rs548422043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, downstream-variant-500B | USP30, USP30-AS1 | GRCh38.p7 | 12:109051761 | TTTTAGTAGAGATGG[A/G]GTTTCACCATGTTGG | 84749 |
| rs548455068 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109026469 | CTTACACAACAGAAT[A/T]TTTTTTTTTTTTGAG | 84749 |
| rs548467227 | in-del | -/TGGCCATTT | 0.00478085 | 0.0486577 | intron-variant | USP30 | GRCh38.p7 | 12:109060260 | CTGAAATGTTAGCAG[-/TGGCCATTT]TGGTATTGTGCAGTC | 84749 |
| rs548470119 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP30 | GRCh38.p7 | 12:109080268 | TCGTCTGACCACTCA[A/G]TCCTGTAGGATGCTG | 84749 |
| rs548660519 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109058624 | TTTTAAATTGTCAAG[C/T]TAATAACAGCTTTTT | 84749 |
| rs548720066 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109049911 | CTGTTGAAAATGGTG[C/T]CAATAGACTTGCTGT | 84749 |
| rs548729125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109059224 | TTTGAGACAGAGTCT[C/T]ACCTTTTTTTCCCAG | 84749 |
| rs548731002 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109051342 | GCTCACTGCAGCCTC[C/T]GCCTCCCAGGTTCTA | 84749 |
| rs548761280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109042991 | AAGAAGTGACAAAAA[C/T]TATTTCATTTACAAT | 84749 |
| rs548770604 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109063309 | TTTTACCACATTGGC[A/C]AGGCTAATCTTGAAC | 84749 |
| rs548784843 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109036269 | GTTAGTGCCCTTTCA[C/T]TTTAGCCCAAAATGT | 84749 |
| rs548857692 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109063880 | TTGAATTGGGTTTCT[A/T]TTTTTTTTTTTTTTT | 84749 |
| rs548871566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109070164 | GGCAAGAATGCAAGC[C/T]GAGAGGAAAGGTGGG | 84749 |
| rs548906972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109029608 | CCAAGAGACTTTCCA[C/T]CCTCCCTCCGTGCCT | 84749 |
| rs548948502 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109033656 | GAATAAAACATTGAT[C/G]GAAAGTCCCTAGTCT | 84749 |
| rs548958317 | in-del | -/ATAG | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109045852 | ACACGTATAGATCAT[-/ATAG]ATACAGACATAGACA | 84749 |
| rs549029493 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109081488 | GCTCAGGCACTATGT[A/G]TAATTCAGATACATG | 84749 |
| rs549117478 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109077414 | ATGATGAGTTAACTC[A/G]TCTTGTCATGATAAA | 84749 |
| rs549146061 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109035553 | ATTTTTAGTAGAGAT[C/G]AGGTTTCACCATGTT | 84749 |
| rs549187770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109078114 | TTTTTGAGGAACCTC[C/T]TCCGTACAATTTTCC | 84749 |
| rs549309679 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109042202 | AAACTTCTGATGAGC[-/T]TTTTTTTTTCCAAAA | 84749 |
| rs549343923 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109041872 | ATTGAAGCACAACCA[C/G]AAAAAAATAGTTTGA | 84749 |
| rs549365635 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109048300 | ATGTTGCCCAGACTC[A/G]TCTCAGACTCCTGGG | 84749 |
| rs549368406 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109077515 | TAATGTTTATTTGGT[A/C]ATTTCTTTCTGTCAT | 84749 |
| rs549439325 | snp | C/T | 1.66142e-05 | 0.00288216 | synonymous-codon | USP30 | GRCh38.p7 | 12:109084975 | TCAGCCAGGGGCCCC[C/T]AAAACACAGATTTTT | 84749 |
| rs549457547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109041533 | CCACCTATTCCAGAG[A/G]CTGAGGCAGAGGAAT | 84749 |
| rs549458581 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109040641 | GGGCTGGAGGATCCA[A/C]TTTCAAGATGGTGCA | 84749 |
| rs549474957 | in-del | -/AC | 0.00795532 | 0.062565 | intron-variant | USP30 | GRCh38.p7 | 12:109084230 | AAGATCCTGTCTAAA[-/AC]ACACACAAAAAATGT | 84749 |
| rs549555614 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109072038 | GTAACAGTATAAATA[G/T]CGGAGGAGTTGACAA | 84749 |
| rs549557378 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109086960 | GATTTGATGACCACC[A/G]AAGTTCAGCCCTTTT | 84749 |
| rs549570715 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109047631 | GACAAAAGGAAGCAA[C/G]CTCTGCATATTTGAA | 84749 |
| rs549577973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109036457 | AGGTGTGAACCACGC[C/T]CAGCTAATTTTTGTA | 84749 |
| rs549615184 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054914 | TGATTATTATAAAAC[A/C]GGGTCAATATTACCA | 84749 |
| rs549731950 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109056888 | AGGTTGGTCATATTT[G/T]TTCTCTGTATCTTTA | 84749 |
| rs549792524 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109028051 | GCACATTCTCCTCAA[C/T]ACTTGTTGATAATAG | 84749 |
| rs549850882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109037423 | CTGGACTTCCTCAAA[C/T]ACAATTTTTACTGTT | 84749 |
| rs549967431 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109064821 | GCCCCATAGTATTTT[A/G]GACAAAGTTGGGTTA | 84749 |
| rs550042494 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109064094 | GGCCAGGATGGTCTC[G/T]ATCTCTTGACCTTGT | 84749 |
| rs550117748 | snp | C/T | 0.000399281 | 0.0141238 | missense | USP30 | GRCh38.p7 | 12:109085672 | TATCATTCAGCTCCT[C/T]CACATACCTCTTCCG | 84749 |
| rs550205804 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109078588 | TGGGCGACAAAGCGA[A/G]ACTCCATCTCAAAAA | 84749 |
| rs550230442 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109036762 | TCCTTCTACTACCTT[C/T]GGACCACCAAGGTTT | 84749 |
| rs550268732 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109068460 | GGTGTTCTCTTGTTT[C/T]TGCTTTATTCTGAAG | 84749 |
| rs550297383 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109070746 | AGTTGATCCTTCAAG[A/T]GTAGTCCCATGCCAT | 84749 |
| rs550339253 | in-del | -/TTTTTTTTTTTCTTTTTTT | | | intron-variant | USP30 | GRCh38.p7 | 12:109079340 | TTTCTTTTCTTTTTC[-/TTTTTTTTTTTCTTTTTTT]TTTTTTTTTTTTTTT | 84749 |
| rs550342638 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109023201 | CCTTTTCCCTCAATC[C/T]TGGTGTCAGGTGGGG | 84749 |
| rs550372748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109076267 | CCTTATATCTTGAGA[C/T]TTTTGTAAACATTCA | 84749 |
| rs550407050 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109085490 | ACATATACTCATAGA[A/C]TGTACATCTTGCCAT | 84749 |
| rs550455607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109042721 | GCTTTCACAACTTCT[A/G]TTTAACGTAGTACTG | 84749 |
| rs550485966 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109082482 | CCTCCACTGTTTCTG[C/T]TATTTAATGACTAAG | 84749 |
| rs550496385 | in-del | -/T | 0.00182449 | 0.0301483 | intron-variant | USP30 | GRCh38.p7 | 12:109057914 | TCTTCTTCCCCCTGC[-/T]TTTTTTTTTAGGGCT | 84749 |
| rs550528086 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109064977 | AAAGGGCTAGCCCCA[A/C/G]GGTATATACACACTG | 84749 |
| rs550542920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053745 | GGCCCCACCACTCTC[C/T]TCGTGATGTCATTTT | 84749 |
| rs550607592 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP30 | GRCh38.p7 | 12:109063100 | AGGCTGAATAATATT[C/T]TTTCTATTTTTTTTT | 84749 |
| rs550632993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109069400 | GCACCTCTGGTGTGC[C/T]GTTGGCTAATAGCTA | 84749 |
| rs550641319 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP30 | GRCh38.p7 | 12:109044375 | AGACATGGTGGCTCA[C/T]GCCTGCGATCTGAGC | 84749 |
| rs550643022 | snp | A/T | 0.000399281 | 0.0141238 | missense | USP30 | GRCh38.p7 | 12:109082958 | TGATGGACATTTACA[A/T]GTACCACCTCCTTGG | 84749 |
| rs550654697 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054983 | AATCAAAACAATATT[C/T]ACATGATCCAAATAC | 84749 |
| rs550741741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109048422 | TAAATATTTCTGTTT[C/T]CATCAGTGATTGCCA | 84749 |
| rs550755498 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109025315 | TGTATTATATGAGAG[A/T]TACCTTATATTTATA | 84749 |
| rs550783904 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109060301 | TGGTAATTTTAAAAT[C/T]ATTTTTGGAAAAAAA | 84749 |
| rs550784333 | in-del | -/TGTG | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109074705 | GATTTGATGTATGAC[-/TGTG]TGTGTGTGTGTGTGT | 84749 |
| rs550818746 | snp | A/G | 0.000996938 | 0.0223041 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052641 | GGCGGCGGCGGCGGT[A/G]GCGGAGGAGACGGTT | 84749 |
| rs550821737 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109033384 | GGAGCTGGCAAATTC[G/T]GACTGGTGAGTGACA | 84749 |
| rs550884895 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109061905 | TTTCTATGCATCCAT[A/T]GAAATTATATATTGT | 84749 |
| rs550902771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109026496 | TGAGACAGGGTCTCT[A/G]TCACTCAGGCTGGAA | 84749 |
| rs550914246 | snp | A/T | 0.000399281 | 0.0141238 | synonymous-codon, utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109067543 | GTCCTGCCAAGAAGT[A/T]ACTGATGATGAGGTC | 84749 |
| rs550934249 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046941 | ACCTCAGGTGATCCA[A/C]CCGCCTGGGCCTCCC | 84749 |
| rs550982108 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022048 | TTATTGTAGAGATGG[A/G]GTCTTGCTTTGTTGC | 84749 |
| rs551019082 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109040731 | TGGACCTCTCCATAA[G/T]GCTGCCTGGGCATCT | 84749 |
| rs551099373 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109031740 | ATGCTTAGTGAGATA[A/C]GCCAGTAACAACAAA | 84749 |
| rs551140974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109049172 | TTGACTAAATGTTTG[A/G]TGCAAGAAGTCTTGC | 84749 |
| rs551163965 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109069549 | TTATATAGGCAACAA[C/G]TATTTATTGAATGCC | 84749 |
| rs551213004 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109076785 | CGCCCAGGCTGGAGT[G/T]CAGTGGCGTGATCTC | 84749 |
| rs551280755 | in-del | -/A | | | intron-variant | USP30 | GRCh38.p7 | 12:109044924 | TTAATCTGATGGGGG[-/A]AAAAATGTTTTCTGA | 84749 |
| rs551335086 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109077989 | TTATAAACCTCACAA[C/T]ACTGTGTCATAGTTT | 84749 |
| rs551346717 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109048061 | GATCATGGGTCTGAC[A/G]TCTAATAGAATGCCT | 84749 |
| rs551386061 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109059945 | ATTATAATGGCAAAA[A/G]GAAAGAATGTAGATA | 84749 |
| rs551415677 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109082283 | TGCTGCAGTTGCCTC[C/G]AATCCCATTTGTTTT | 84749 |
| rs551426307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109041451 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCATC | 84749 |
| rs551428673 | in-del | -/A | | | intron-variant | USP30 | GRCh38.p7 | 12:109066248 | TGAGACCCTGTCTCA[-/A]AAAAAAAAAAAAAAA | 84749 |
| rs551452796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109044552 | TAGGGTGGAAGGATC[A/G]TCTGAGCTCTGGAGT | 84749 |
| rs551503339 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109049756 | AGGAGGTGGAGGTTG[A/C]AGTGAGCCAAGATTG | 84749 |
| rs551522430 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109048995 | CTGACCTCTCATCTC[A/G]TTATGGCTGGGAACT | 84749 |
| rs551550919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109042120 | AGGACACCCACACAT[A/G]GGTATCTTCATACGA | 84749 |
| rs551556601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109077860 | GAGAGATTACGTTAT[A/G]CAGTTTTACCTTATC | 84749 |
| rs551562966 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109084373 | ATTACACGTTGGTAT[C/T]CCTTAGAAGCTGACA | 84749 |
| rs551587541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109033565 | TGGCCTCTTGACTCT[A/G]TTTCAGTTGGGTATG | 84749 |
| rs551588731 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109041240 | CAGGCAAATGCAATT[A/C]TTGCTGGGGAAAACA | 84749 |
| rs551612996 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109069269 | CCACCTCCATCCTTT[A/C]TCGGATCTGCTTCAA | 84749 |
| rs551644271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109062563 | TCAATCTCCTGACCT[C/T]GTGATCCGCCCGCCT | 84749 |
| rs551705208 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109061647 | ACTCCTAAGCTCAAG[C/T]AATCTGCCTGCCTTG | 84749 |
| rs551706249 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109047566 | CATTATACATGTTCA[C/T]GTGAAAGCATCTTGT | 84749 |
| rs551815456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109032554 | CATAGAAGGCCACAT[A/G]TTGTACATATTGTGT | 84749 |
| rs551911729 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109051273 | TTTTTTTTTTTTTTT[-/TT]GATGCTGAATCTCTC | 84749 |
| rs552168595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109074128 | ATGGAATCATGTAAT[A/G]TGTGGCTTTTTGTGT | 84749 |
| rs552191717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109039872 | CCTTGGCCTCCCAAA[A/G]TGCTGGGATTACAGG | 84749 |
| rs552208209 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109057199 | TAAAAAATTATTTTC[-/T]TTTTTTTTTTAATGC | 84749 |
| rs552211546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109074748 | GTGCTCATATGTGGT[A/G]AGAACACTCTCTTAG | 84749 |
| rs552324915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109080421 | CTCCGTTCATTCAAA[C/T]GGTTTTGTTTTGTTG | 84749 |
| rs552337571 | snp | A/G | 0 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109068378 | AACTGTGGGGCCGAC[A/G]TGAGGGGCATCGAGA | 84749 |
| rs552341583 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109043495 | AAGGACAGTCTTCAT[C/G]AAATAGTTCTGGGAA | 84749 |
| rs552359918 | snp | C/T | 3.29745e-05 | 0.00406031 | intron-variant | USP30 | GRCh38.p7 | 12:109081302 | GAACTAAGCCTAAAT[C/T]GTTTCTGGATTTTCT | 84749 |
| rs552405846 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054445 | AGGATCACCTGAGCC[C/T]GGAAGGTGAAGATTG | 84749 |
| rs552413843 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109039408 | AAGACAGGAGATAGG[A/G]CTTGTGTTCTAGTCA | 84749 |
| rs552525240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109030086 | CCTGCAAGTTACGCT[A/G]TAAGATTAAGGCAGG | 84749 |
| rs552752395 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, nc-transcript-variant | USP30, USP30-AS1 | GRCh38.p7 | 12:109052522 | CGGGGGCAGCTACTT[C/T]CGGTCCCCCTGGGAG | 84749 |
| rs552803896 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109049881 | TGTGGTACAGAGACA[C/T]GAAGTGAGCACATGC | 84749 |
| rs552821437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109047129 | TAAAACCACCTTTTA[C/T]TCCTCCAACGGGTTT | 84749 |
| rs552834097 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109023009 | GCACTACATTTGGTA[C/T]CACATGATTCCTGGC | 84749 |
| rs552843882 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109082256 | CTGAGATGAGAAATG[A/C]CCTCTCCAGTTTGCT | 84749 |
| rs552920071 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109023899 | CGGCCTCCCAAAGTG[C/T]TGGGATTACAGGTGT | 84749 |
| rs552938945 | snp | C/G | 5.52135e-05 | 0.00525392 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052773 | TCAGGTGAGATTTTG[C/G]GGGGCGGGGCTGCCG | 84749 |
| rs552970975 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109060564 | TGTGCAACTCGCTGC[A/C]AGCGTTCATCTAATT | 84749 |
| rs553009958 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109060903 | CACCTGCCTTGGCCT[C/T]CCAAAGTGTTGGGAT | 84749 |
| rs553085728 | snp | C/G | 9.93229e-05 | 0.00704639 | missense | USP30 | GRCh38.p7 | 12:109073450 | CAGGGTCACCTCACC[C/G]TACATCCAATCACTG | 84749 |
| rs553154130 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109058947 | TTAGTGCCACTTTTC[G/T]GGAAAGCAGTTTGGA | 84749 |
| rs553189594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109031194 | TTTAATTTATTAATG[C/T]GACTACACGCATTGG | 84749 |
| rs553224647 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109048016 | CCAGTGTATCTCGGA[A/G]TTTTCCAGAGGCCGT | 84749 |
| rs553256737 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP30 | GRCh38.p7 | 12:109058367 | CGAGGTCAGGAGTTC[A/G]AAACCAGCCTGACCA | 84749 |
| rs553335750 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109063360 | CCCACCTCAGCCTCC[C/T]AAAGTTCTGGGATTA | 84749 |
| rs553398927 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109066654 | CACGCCATTGCACTC[C/T]ACCCTGGGCGACAGA | 84749 |
| rs553398944 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109030893 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGTGCC | 84749 |
| rs553418745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, downstream-variant-500B | USP30, USP30-AS1 | GRCh38.p7 | 12:109051908 | GTGGCTACTGGAAAA[C/T]GTAAAATTACCTATG | 84749 |
| rs553431867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109065182 | TGTATCTTGGGAGTC[A/G]CTGAACTTCCAGAAA | 84749 |
| rs553464849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109038837 | TATTATATAATGGTG[C/T]TAATTTTTGTATCCC | 84749 |
| rs553536789 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109025320 | TATATGAGAGATACC[G/T]TATATTTATATCTAT | 84749 |
| rs553596458 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109023094 | ACTTGTCAGTATCCC[C/T]ATTGTTGCATAGCTG | 84749 |
| rs553609759 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109035679 | CATTTTGATTTATAA[C/G]AATCTAGTTTGGATT | 84749 |
| rs553611600 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109044331 | TGTCTTTCAATACCA[A/C]TGAACTGCACACTTA | 84749 |
| rs553662047 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109045233 | ATCCACCCGCCTCGG[C/T]CTCCCAAAGTGCTGG | 84749 |
| rs553680104 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109079875 | GAGGTCCTCGTGTGC[C/T]GACTTCTTTGTATTT | 84749 |
| rs553713046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109029169 | TCTCACAGAAAGATA[C/T]TGGCTGCAGCTTGGT | 84749 |
| rs553830418 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109028534 | CCAGACTGGAGTGCA[A/T]TGGTGTGGTCTCAGC | 84749 |
| rs554023720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109077720 | CATATTTTCTTGTTC[C/T]TCTGTTCCCCCTTCA | 84749 |
| rs554038991 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP30 | GRCh38.p7 | 12:109083245 | AAGAGGTTAAAATTA[C/T]GTAGCAGTGAGATGT | 84749 |
| rs554127064 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109023308 | CTATAATCCCAGCAC[C/T]CTGGGAGGCCGAGGC | 84749 |
| rs554172688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109063427 | ATATTCTGTTGCATG[C/T]ATATGCAGCATTTTG | 84749 |
| rs554209713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109064179 | GCTCAGCATTGTTTG[A/G]TTTTTTGTTGTTGAG | 84749 |
| rs554213738 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109030075 | TTCACCTTCTTCCTG[C/T]AAGTTACGCTGTAAG | 84749 |
| rs554239376 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109058971 | GTTTGGAACTACACA[A/G]TAATAGCTTGCGAAA | 84749 |
| rs554262662 | in-del | -/A | | | intron-variant | USP30 | GRCh38.p7 | 12:109058714 | CAAAAACATTAAAGT[-/A]AAAAAAAAAATGTCC | 84749 |
| rs554363345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109066664 | CACTCCACCCTGGGC[A/G]ACAGAGCACGACTCT | 84749 |
| rs554419581 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109027388 | GGCAATCCTCCCACC[C/T]CAGCCACTGGAGTGG | 84749 |
| rs554449000 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109069847 | TTCAGCGGAGACCGG[A/T]AGTATAAAAGAGAGT | 84749 |
| rs554487408 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109070280 | GTATTTTGGAGGAGG[A/G]TCCTTTTTTCAGGAC | 84749 |
| rs554488575 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109029865 | GGTAGGGTGAGAGGG[G/T]CAACCTTTGATTAAC | 84749 |
| rs554524038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109072710 | TCATCCTTAGGAGGA[A/G]ATTGTTGTTTTCTTA | 84749 |
| rs554556525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109066295 | GTTTATTTTCTGGAC[C/T]TTTACAGAAAAAGTG | 84749 |
| rs554581368 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109051000 | ATCTCAAAAAAAAAA[-/G]AATGTAAATTATCTC | 84749 |
| rs554685886 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109050220 | AATCACTTGAACCCG[C/G]GAGGCGGAGCTTGCA | 84749 |
| rs554692124 | snp | C/T | | | utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109024854 | TCGATCTCCTGATCT[C/T]GTGATCCACCTGCCT | 84749 |
| rs554719750 | in-del | -/CA | 0.00159617 | 0.0282053 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109086915 | AGTCTCTCTGAACCT[-/CA]GTTTCCTCATTTGTG | 84749 |
| rs554730100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109036708 | CCAGATATAGTATTA[C/T]TGTTGACAGCTTTGT | 84749 |
| rs554848034 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109080032 | AACTCAACTCTGTCT[C/G]CCCTACATTGGGCAG | 84749 |
| rs554852070 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088150 | GTAAGGGAAATGCCA[A/G]CTCCCTCTTAGAGTC | 84749 |
| rs554904878 | snp | C/G/T | 0.00319074 | 0.0398324 | intron-variant | USP30 | GRCh38.p7 | 12:109084724 | AGATCCCAGGCTAGC[C/G/T]GTAAAGCTGGAGCTA | 84749 |
| rs554908730 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109086352 | GACAAGAATTAATGA[A/C]ATTATTAAAGGCAAC | 84749 |
| rs554972051 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109077827 | TGTGTGTTTGTGTTG[G/T]GGGGGGAGGGTGTGT | 84749 |
| rs554992678 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109085324 | GTATGTATAAAATAT[A/T]AAGAAAATTTAAAAT | 84749 |
| rs554999941 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054284 | CCAGCTCTTTGGAAG[C/G]CTGAGGCAGGTGGAT | 84749 |
| rs555022208 | snp | C/T | 1.66994e-05 | 0.00288953 | synonymous-codon, intron-variant | USP30 | GRCh38.p7 | 12:109058098 | CTTAACACTCTTGCA[C/T]CTTCTGAAAGGTATC | 84749 |
| rs555062214 | snp | A/G | | | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109021860 | TTTTATTTTTTCAAT[A/G]TTTATTTATTTATTT | 84749 |
| rs555089015 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109044499 | AAAATCAGCCAGGCA[A/C]AAAGGCTCGTGTCTG | 84749 |
| rs555110322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109062574 | ACCTCGTGATCCGCC[C/T]GCCTTGGCCTCCCAA | 84749 |
| rs555147365 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055374 | TACACACACACATAT[A/T]TATACATATATATAT | 84749 |
| rs555154192 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109071075 | GAGGTTCCCAGAGTA[A/G]TCAGATTCCTAGAGA | 84749 |
| rs555155969 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109078318 | AATCCCAGCTACTCG[G/T]GAGGCTGAGGCAGGA | 84749 |
| rs555183418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109028277 | TTTGTATTGCTGTAA[A/G]GGAATACCTGACACT | 84749 |
| rs555240285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109064329 | GAGTGCAGTGATGCA[A/G]TCTCAGCTCACTGCA | 84749 |
| rs555244691 | snp | C/T | | | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109087305 | AGGTAAGGCTAAGAC[C/T]GCACTTCCTCTGCTG | 84749 |
| rs555332935 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109057130 | ATACATTTGTGTTCT[C/G]TCAGACTAGCTTGCT | 84749 |
| rs555361073 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109042211 | ATGAGCTTTTTTTTT[C/T]CCAAAAGGAATGTCA | 84749 |
| rs555367796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109048561 | CCTGGCCAACATGGC[A/G]AAACCCCATCTCTAC | 84749 |
| rs555437813 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109062169 | TGAACTCCTGGGCTC[A/G]GGTGATCCACCCGCC | 84749 |
| rs555447895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109076591 | TTTATCATACTGACA[A/G]ACTTCCCTTCTGTTC | 84749 |
| rs555473310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054335 | AGACCAGCCTGGGCA[A/G]TGTAGTGAGACCCTG | 84749 |
| rs555486630 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109068887 | GCCTTGCCCACATCT[A/T]TATTATCAGCGATCC | 84749 |
| rs555600371 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109031923 | AGCCCTGACAACATA[A/G]CAAGACCTCATCGCT | 84749 |
| rs555600376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109040846 | TTTGGAATTCACATA[A/G]CATCACTCTCACAAT | 84749 |
| rs555644755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109070315 | GCTGAATTGGCTGAG[A/G]GTGGGTTAGAGTTCA | 84749 |
| rs555664680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109049360 | CCTGAGAAGAGTGAG[A/G]GAGAGGGGGGAACAG | 84749 |
| rs555694961 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109078380 | GGTGAGCCGAGATCA[C/T]GCCACTGCACTTCAG | 84749 |
| rs555823979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109079716 | TGCAACAAATTTTTC[A/G]TCGTAATCACTGTTG | 84749 |
| rs555954364 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109033862 | TCCCTGGGTCACATA[A/G]CTCATCCCTCCATGA | 84749 |
| rs555957980 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109067066 | AAGCTACAAAGAATG[A/G]TGAAAAATACCTAAT | 84749 |
| rs555962982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109049370 | GTGAGAGAGAGGGGG[A/G]AACAGCCAGTCAGTG | 84749 |
| rs555999663 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109049952 | CCACAAACCTTGAAC[C/T]TGTAAAAATGCAGTA | 84749 |
| rs556011396 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109075458 | TGGGTTCAAGCAATT[A/C]TCCCACCACAGTCTC | 84749 |
| rs556069207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109025729 | CAGGCTGGAGTGCAG[C/T]GGTGTGATCACAGCT | 84749 |
| rs556078847 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109043151 | GGAAGAATTAATATC[A/G]TTAAAATGTCAATAC | 84749 |
| rs556079319 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109085975 | TGGCACTGTCTGCAC[C/T]GTCCAGGAAAAAAGT | 84749 |
| rs556081779 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109083785 | CAGTTAGGTCAGGAT[G/T]GTCTCACACCCCATA | 84749 |
| rs556101858 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109035612 | AGTGATCCGCCCACC[A/T]CGGCCTCCCAAAGTG | 84749 |
| rs556110076 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109069872 | GAGAGTGAAGTGTGT[A/G]GACACCTGGGTACAG | 84749 |
| rs556135796 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109042351 | TGTCCTCAGTCATAC[A/G]GTTCTTTTCCCAAAG | 84749 |
| rs556200841 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109085476 | CATATACACAATATA[A/C]ATATACTCATAGAAT | 84749 |
| rs556238387 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055495 | GTAACCTCCGCCTCT[C/T]GGACTCAAGCCATTC | 84749 |
| rs556258071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109069799 | CAGGGGGAGACTGCT[C/T]CAGGTAGGGAGGCTC | 84749 |
| rs556259009 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109028469 | TTTTTTTTCTGTTTT[G/T]TTGTTGTTGTTGTTG | 84749 |
| rs556275173 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109048745 | ACTCTGTCTCAAAAA[A/T]AAAAAAAACAAAAAA | 84749 |
| rs556408227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109026328 | TGATCCACCCGCCTT[A/G]GCCTCCCAAAGTGCT | 84749 |
| rs556444439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109026745 | AGTGTTGAGATTACA[A/G]GTGTGAGCCACTACA | 84749 |
| rs556607870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109070228 | GCTCAGACTGGGGTC[A/G]AAGCAGGGTAGCTGA | 84749 |
| rs556730939 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109044808 | TTGTAATTCTGATAA[A/G]CATCCAAATTGCTCT | 84749 |
| rs556766651 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109062987 | ACCTCATTAAGCGGA[C/T]TCATATAATATTCAC | 84749 |
| rs556782954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109033833 | ATAATGTAAAGGTGC[A/G]CAACTTTAAGGAGTC | 84749 |
| rs556820584 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109040945 | ACACTCAGCTTTTCT[C/T]CCATATTGCCCTACA | 84749 |
| rs556842602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109084573 | ATGCACAGGACAGCC[C/T]CCGCAACAAAGAATG | 84749 |
| rs556842638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109076831 | CCACCTCCCAGGTTC[A/G]CGCCATTCTCCTGCC | 84749 |
| rs556844781 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109027330 | GCTGTCCAGGTTGAC[A/G]TGCAGTGATGCAATC | 84749 |
| rs556895145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109081645 | CACACACACACACAC[A/G]CACACACACACACAC | 84749 |
| rs556970811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109040373 | AAGCAGCTCAAGAGA[C/T]TTTGAGGTAGTTGGT | 84749 |
| rs556974159 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109060949 | CCATGCTTGGCCTTT[C/T]TAATTTTTTTAAAAA | 84749 |
| rs556980563 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP30 | GRCh38.p7 | 12:109082359 | AACTTGAGTTTTCCC[C/T]TCTGACTCAAGAGGA | 84749 |
| rs557104741 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046192 | TGGAACCTCCGCCCC[C/G]CCGGGTTTAAGTGAT | 84749 |
| rs557116870 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109074491 | TTTTTCATTCCCACC[A/G]GCAGTGTATGAGGGG | 84749 |
| rs557154425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, downstream-variant-500B | USP30, USP30-AS1 | GRCh38.p7 | 12:109052034 | ACTTACTATTTCTTC[A/G]AATTTCCTGGGTTCC | 84749 |
| rs557170521 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109024077 | CCTCTTCCTGGGTGG[G/T]TAACCTCGAGCAGGT | 84749 |
| rs557459136 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109031272 | TGTCCATCATTTTTA[G/T]GGAACAGTTTCATTC | 84749 |
| rs557494156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109068784 | AGTCACTGAGCCCAC[A/G]TCGTGCTGTAGTCTG | 84749 |
| rs557668123 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | USP30 | GRCh38.p7 | 12:109061936 | AGGTTTTTTTGTTTT[C/T]TGTTTTGTTTTTGTT | 84749 |
| rs557810319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109041073 | GGTCCTCTGTTTCCT[C/T]ATCAGTCAACTGAGC | 84749 |
| rs557810505 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109076446 | CTTATTATCCTGGCT[A/C]AGACTTATGGTACAA | 84749 |
| rs557849104 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109050533 | ATGCGACACCACCCC[A/C]AGCATGAATGCAATT | 84749 |
| rs557935348 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109025680 | GAAGTGGAACTGCCA[C/G]TTTTTTTTTTTGACA | 84749 |
| rs557942063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046547 | CAAAAACCATCTCAC[A/G]GAAACATCCAGACTA | 84749 |
| rs557991172 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046990 | GGGTTGAGCCACTGC[A/G]CCCGGCCAGCTGGAA | 84749 |
| rs558343306 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB, downstream-variant-500B | USP30, USP30-AS1 | GRCh38.p7 | 12:109051770 | AGATGGGGTTTCACC[-/A]TGTTGGCCAAGCTGG | 84749 |
| rs558359306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109060484 | TTCTGTGGAAGAGGT[A/G]ACTTGGGAATAATTT | 84749 |
| rs558388070 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | USP30, SVOP | GRCh38.p7 | 12:109021175 | TGGCTGATGGTGTAT[C/T]ACTGGGATGCCTATA | 84749 |
| rs558431244 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109024169 | CTTCATAGGGTGGTG[A/G]TCAGAATCAAAGATA | 84749 |
| rs558443470 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109082476 | CTCTTCCCTCCACTG[C/T]TTCTGTTATTTAATG | 84749 |
| rs558443786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109038728 | ATTATTTTACATTCC[C/T]GCTAGCAACGTATGA | 84749 |
| rs558468581 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109031433 | TTTAAAATTTGCCAC[G/T]GACAGTTTCTTTAAA | 84749 |
| rs558510996 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109050111 | GCAGCCTGGCCAATA[C/T]GGTGAAACCCTGTCT | 84749 |
| rs558512230 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109081604 | TTTTGGCTTTTTGAA[A/T]ACACACGCACGCATG | 84749 |
| rs558526460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109059674 | GCATGCCACCACGCC[C/T]GGCTAATGTTTGTAT | 84749 |
| rs558535241 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109030614 | CAAAAAGGTAGGTTG[C/T]TTGTTTGTTTGTTTG | 84749 |
| rs558674255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109080913 | CACCATCTAGGTTCT[C/T]GTAAGCGCGCTCTGC | 84749 |
| rs558696094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109029919 | GGCCTCTGAGAAAGT[C/T]CCCCGAGTTCTCCAG | 84749 |
| rs558978802 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109083392 | TGAATTTCTTTTTTC[A/G]GTCATGTCATTTCCT | 84749 |
| rs558981495 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109028579 | ACCTACCAGGTTCAG[A/G]CAATTATCCTGCCTC | 84749 |
| rs559016875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109051384 | GCCTCAGCCTCCCGA[A/G]TAGCTGGGATTACAG | 84749 |
| rs559017880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109039198 | GCAAAGATTTTTCTC[C/T]GTTTTCCTCAGAAAG | 84749 |
| rs559046566 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109050687 | AAAGTGGGTACTCCA[A/G]ACTGAGAGGTACTTA | 84749 |
| rs559052434 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP30 | GRCh38.p7 | 12:109038892 | TTTTCATGTGCCTAC[C/T]GATCATTCTCATATA | 84749 |
| rs559054450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109039766 | CAGGTGCCCGCCACC[A/G]CACCCAGTGAATTTT | 84749 |
| rs559054707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, nc-transcript-variant | USP30, USP30-AS1 | GRCh38.p7 | 12:109052477 | TAAGGGAAAAGAAAG[A/G]AAGGACGTGGTCCGT | 84749 |
| rs559091825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046049 | AGGCAGTCTGCAAGC[A/G]GAATTCCCTCTTATT | 84749 |
| rs559136644 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | USP30 | GRCh38.p7 | 12:109069660 | TGGTATTCCAGTGGG[A/G]GATGAGGATAGCAGG | 84749 |
| rs559202957 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109058281 | ATTTTTTAAAAATCA[A/C]AGATGGAGGCCGGGT | 84749 |
| rs559348518 | in-del | -/C | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | USP30, USP30-AS1 | GRCh38.p7 | 12:109052556 | CCTGCGGTCTACGTT[-/C]CCCCCGAGGTGCTGG | 84749 |
| rs559389118 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109081610 | CTTTTTGAATACACA[C/T]GCACGCATGCGCGCA | 84749 |
| rs559523220 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109071155 | AGTGTTTAACAGATA[C/G/T]GGAGTTTCAGCTGGG | 84749 |
| rs559546339 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109029954 | CCCATAATCCCTCCT[C/G]TCCCATCTGTACAAC | 84749 |
| rs559554714 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109040776 | CTGGCTTTTCCCAGA[G/T]CAAGTGTTTCAAGAA | 84749 |
| rs559557934 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109086397 | AGTGCCTTTCACTTT[C/T]GATTGCTTTTGTAGC | 84749 |
| rs559560376 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109066481 | TGAGGTTAGGAGTTC[A/G]AGACCAGCGTGGCCA | 84749 |
| rs559593024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, downstream-variant-500B | USP30, USP30-AS1 | GRCh38.p7 | 12:109051724 | ACAGGAGCCTGCCAC[C/T]ACGCCCGGCTAATTT | 84749 |
| rs559630762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109045483 | CCTGAGGGCTCAGGT[C/T]GGAGGCAGAATTGTC | 84749 |
| rs559642526 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109087587 | TACCCAAGTCTGGTG[A/G]AACAAATGCCCAATC | 84749 |
| rs559674515 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP30 | GRCh38.p7 | 12:109071306 | CAATTAACAAAAAAC[A/G]TAATCTTTTGAAATC | 84749 |
| rs559696251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109050931 | ATAATCGCTTGAACC[C/T]GAGAGGCGAGATCGT | 84749 |
| rs559701823 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109028541 | GGAGTGCAATGGTGT[G/T]GTCTCAGCTCACTGC | 84749 |
| rs559716566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109029553 | TAGGGCACACTGTTT[C/T]ACTAGGGCCCATTGT | 84749 |
| rs559758352 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109064531 | AGTGATTAACCACCT[C/T]GGCCTCCCAGAGTGC | 84749 |
| rs559784760 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109025892 | GGAGTTTTGCTTCAT[C/T]GCCCAGGCCGATCTC | 84749 |
| rs559870359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109065565 | AAAAACGGAGGTACT[A/G]AACAGAATTATAACA | 84749 |
| rs559878797 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109021401 | AGGCACTGGGGGTAT[A/G]ACAGAACAAATTCGA | 84749 |
| rs559935742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109056612 | TGACAAAATGTTATT[C/T]TGTCTATATCTGTAT | 84749 |
| rs560032028 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109070552 | ATGGTAGGTTTTACT[C/G]TAGTAGTGGAAGCCA | 84749 |
| rs560049497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109078109 | TTAACTTTTTGAGGA[A/G]CCTCCTCCGTACAAT | 84749 |
| rs560108737 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109027125 | AGTTTGAAGTGTACA[A/G]TTTAGTGGCTTAGAG | 84749 |
| rs560247651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109042587 | TATATAATAATTTTG[C/T]TGGATATTTAAATTG | 84749 |
| rs560283955 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109085559 | CATTTGGTGGTATGG[A/C]CTTACCATTGTATTC | 84749 |
| rs560320240 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP30 | GRCh38.p7 | 12:109058212 | ATTGTAGGAAAAGAT[C/T]ATACAGATCATTATG | 84749 |
| rs560505459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055560 | ACCTGCCACCACACC[C/T]AGCTAATTTTTGTAT | 84749 |
| rs560542360 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109048818 | AAGTGCAGGGGTGTG[A/T]AACGCAATCCTTGCT | 84749 |
| rs560561864 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109058408 | ACTCCATCTCTACTA[A/C]AAACACAAAAAATAT | 84749 |
| rs560623824 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109069067 | CCCATTTTACAGATG[G/T]AAAAACACTGAGGCT | 84749 |
| rs560703289 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109056318 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 84749 |
| rs560710939 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109062361 | TTTTTTTGAGACGGA[C/G]TCTCGCTCTGTCGCC | 84749 |
| rs560728338 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109028556 | GGTCTCAGCTCACTG[A/C]AACCTCCACCTACCA | 84749 |
| rs560750228 | snp | C/G/T | 4.94616e-05 | 0.0049728 | missense, synonymous-codon, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088424 | AGTCTCTGCAGGCAC[C/G/T]GAAGGAGACAGAGGC | 84749 |
| rs560880766 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109070657 | CCAAAGGAGAAGCAG[A/T]GGGCCTGTGTTGTGA | 84749 |
| rs561067513 | snp | C/T | 0 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109044695 | TATGTTATATGTACT[C/T]TGCCACAATAAAAAA | 84749 |
| rs561086351 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109028034 | CAAGGATTCCAATTT[C/G]TGCACATTCTCCTCA | 84749 |
| rs561186545 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109071344 | AGGTCAAGGCTGTCT[C/T]AGTGAAACAGAATGG | 84749 |
| rs561301046 | snp | A/C/T | 0.000181756 | 0.00953146 | intron-variant | USP30 | GRCh38.p7 | 12:109085642 | TTAAAATTGTAAACC[A/C/T]CTGACATGTGTTCGT | 84749 |
| rs561387090 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109086155 | GTTGTGTTAAGAAAG[C/G]ATTCATTATGTCCGG | 84749 |
| rs561447665 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109077586 | TATAATGGGTCTTGC[C/T]TTTTTAACTAGCTTG | 84749 |
| rs561452149 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | USP30 | GRCh38.p7 | 12:109041890 | AAAAATAGTTTGAAT[G/T]ACAAAGATTGTGACA | 84749 |
| rs561483058 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109077039 | GCCCAGCCAGTGATT[C/G]ATTTTTCTAATGTTA | 84749 |
| rs561507336 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109048370 | GGATTATAGGTGTGA[A/G]CCATCGCGCCTGGCC | 84749 |
| rs561564887 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109056398 | GGGTTTCCACATGTT[G/T]CCCAGGCTGATCTCA | 84749 |
| rs561578252 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109069271 | ACCTCCATCCTTTCT[C/T]GGATCTGCTTCAAGC | 84749 |
| rs561625346 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP30 | GRCh38.p7 | 12:109034225 | TAATGTTTCTCTTAC[C/T]TATTGGCTATTCAGG | 84749 |
| rs561659461 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109049575 | ATCCCAGCACTTTGG[A/G]AGGCCAGGGCAAGCA | 84749 |
| rs561667639 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109084250 | CACAAAAAATGTCAT[A/C]AGGAAACTACTTGGT | 84749 |
| rs561713664 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109031919 | GACCAGCCCTGACAA[C/T]ATAGCAAGACCTCAT | 84749 |
| rs561716572 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109060723 | GCAGTGGCGGGATCT[C/T]GGCTCACTGCAACCT | 84749 |
| rs561725142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109026985 | GTCAGCCCCACCTGC[A/G]TGACCTTCTGTAACC | 84749 |
| rs561755503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109061514 | CCCAGGCCCAAAACA[A/G]TCCTCCATTTCCATT | 84749 |
| rs561840014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053705 | TAGCAGAGTTGGGAG[A/G]AGAAGCCAGATCTTT | 84749 |
| rs561845549 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP30 | GRCh38.p7 | 12:109067271 | GGCACCCACCACCAC[A/G]CCCGGCTAATTTTTT | 84749 |
| rs561930943 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109064703 | TTATACATATCCCTT[G/T]ATGCACCTAAGCATG | 84749 |
| rs561961214 | in-del | -/GGG | | | intron-variant | USP30 | GRCh38.p7 | 12:109036066 | TTGGGAGGCTGAGGT[-/GGG]AGGATTGCTTGAGAC | 84749 |
| rs561963646 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109031504 | CACTCCTAGGTATAT[A/T]CAAAAAGAATTAAAA | 84749 |
| rs561973266 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109041179 | TTTGCAAAGCAATGT[C/G]CTGAAGACTTATGGG | 84749 |
| rs561982357 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109041328 | CTGAAAGCTTGCTGG[A/G]GCTTCATGATTTAAG | 84749 |
| rs562004999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109033194 | AAATATAGAGGTGAA[C/T]CTCTAAACTTAAAAC | 84749 |
| rs562123232 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052918 | GAGGCCTGGGCCCGT[A/T]GGTGGGAGGACTGAC | 84749 |
| rs562192164 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109074634 | GCTTTTTCCCCCAGT[G/T]TTATTGAGATCTAAT | 84749 |
| rs562204021 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109025260 | GGAAATTCTCAGCCT[C/T]CCTAATTATGTTGGC | 84749 |
| rs562271129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109073879 | GAAAATTTCCAACAT[C/T]ATACAAAAAGAGAGA | 84749 |
| rs562325777 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046119 | TTTTTTTTTTTTTTT[-/TT]AGATGGAGTCTCACT | 84749 |
| rs562358538 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109027790 | TTGTTAATCCATTCA[C/T]CTGTTGATGGACACG | 84749 |
| rs562372432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109077221 | TTTGTCAGGCTTTGT[C/T]ATAAGGATTATACTA | 84749 |
| rs562382615 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109028802 | TTTAAACAATCAGAT[A/G]TCTTGTGAACTTACT | 84749 |
| rs562418428 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055825 | TGCATTAAAAAAAAA[A/G]AAAAGAAAAGAAAAA | 84749 |
| rs562460015 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP30 | GRCh38.p7 | 12:109077833 | TTTGTGTTGGGGGGG[A/G]AGGGTGTGTGTGAGA | 84749 |
| rs562517857 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053790 | TTTCCAAAGTCGCCA[C/G]TTGTCCCTGGGTATT | 84749 |
| rs562522298 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109061381 | TGCTTTCCAATGTCT[C/T]TAACTTTGGTTTAAA | 84749 |
| rs562641606 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109048045 | GTACAATGAGTGATG[G/T]GATCATGGGTCTGAC | 84749 |
| rs562726215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109026525 | AATGCAGTGACATGA[C/T]CATGGCTCACTGCAG | 84749 |
| rs562867582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109041264 | GAAAACAACCCATAA[A/G]TTAACAACAAATAGG | 84749 |
| rs562874415 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109062194 | CCCGCCTCAGCCTCC[C/T]GTAGTGCTGGGATTA | 84749 |
| rs562996819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109031592 | AGCCAAACAGTGGAA[A/G]CAACCCATGTGTCCA | 84749 |
| rs563048374 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109069466 | GGGGCTAGAGCCTTG[A/C]CTTATTTATCTTTGA | 84749 |
| rs563081731 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP30 | GRCh38.p7 | 12:109025386 | TTGTTGGTTTTGTCT[A/G]TCCGGAGAGCTCTGA | 84749 |
| rs563302608 | snp | A/T | 1.79939e-05 | 0.00299943 | intron-variant | USP30 | GRCh38.p7 | 12:109082641 | TAGGCATTGCTGCAG[A/T]GAAATGTTCCTTTTA | 84749 |
| rs563388815 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, missense | USP30 | GRCh38.p7 | 12:109083162 | TGACAGGAGCACAAG[C/G]CTTGTACAATGGTGC | 84749 |
| rs563389223 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109043428 | AATACAAACTCTCTG[A/G]TATATGGTCAAAATG | 84749 |
| rs563535786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109087788 | TGTAAATGTGAACAA[C/T]AGCTGTGCAAAGCCT | 84749 |
| rs563598101 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046197 | CCTCCGCCCCCCCGG[A/G]TTTAAGTGATTCCCC | 84749 |
| rs563610023 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046793 | CCTCCACCTCCCAGG[C/T]TCAAGCAATCCTCCC | 84749 |
| rs563616976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109066886 | CAACCTGAAAGTTGT[A/G]AGTTAAAATCATTTT | 84749 |
| rs563627393 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109039300 | TTTTACAATAGTGTA[A/C]CTTCTATATTTTTAT | 84749 |
| rs563653702 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109023781 | GGGATTACAGGTGCC[C/T]GCCACCATGCCTGGC | 84749 |
| rs563679509 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109070872 | CGCAATAGCCAAGGG[G/T]TAGAAGCAACCCAAG | 84749 |
| rs563739944 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109024392 | CCTCCCGAATAGCTG[C/G]GATTACAGGTGTGCG | 84749 |
| rs563740887 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109040608 | CTATGGCTGTGGTCT[C/T]ATCTGAAGACTTGAC | 84749 |
| rs563757941 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109059238 | TCACCTTTTTTTCCC[A/G]GCCTGGAGTGCAGTG | 84749 |
| rs563761761 | snp | A/C/T | 8.24129e-05 | 0.00641876 | missense, synonymous-codon, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088412 | GCCGGAAGACAAAGT[A/C/T]TCTGCAGGCACCGAA | 84749 |
| rs563784202 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109038210 | GTTGGTTCCCGCCCC[C/G]CTCCCCACCTGCCAG | 84749 |
| rs563927143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109029614 | GACTTTCCACCCTCC[C/T]TCCGTGCCTGAGCTA | 84749 |
| rs563948229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109032116 | AAAAAAAAAAAAACA[C/T]GGGCAACATGGTGAA | 84749 |
| rs563952379 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | USP30 | GRCh38.p7 | 12:109075847 | TTACTTTTTCTTTTT[C/T]TTTTTTTTTTTGCTG | 84749 |
| rs564096240 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109074490 | ATTTTTCATTCCCAC[C/T]GGCAGTGTATGAGGG | 84749 |
| rs564178093 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109067447 | TTAATTAACTTTGAT[A/G]TGTTATACTGTGCAA | 84749 |
| rs564186856 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109068407 | GAGACTTTTGGAAAG[A/G]GAGCTGGGGAGGCTT | 84749 |
| rs564254749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109026396 | TAATTTTTATTGTGG[C/T]AAATACATATGTCTT | 84749 |
| rs564276229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046855 | GTGTGCGCCATCATG[C/T]CCAGCTAATTTTTGT | 84749 |
| rs564308153 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053629 | CTGAAAGTCCTCGAT[A/G]CTTATCCTGTCCAGT | 84749 |
| rs564362289 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109047322 | CAGTGCTAAGAATGT[A/G]CTGCCAACATAATTG | 84749 |
| rs564366617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109073070 | ATTCAGAACTTGCTT[A/G]TTCTGTTTATTTCAG | 84749 |
| rs564369765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109039874 | TTGGCCTCCCAAAGT[A/G]CTGGGATTACAGGCG | 84749 |
| rs564400837 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109060686 | TTTGAGATGAGTCTC[A/G]TCTTGTCACTCAGGC | 84749 |
| rs564452304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109073659 | TGGCCTCTGCACACT[A/G]GTGGACTGACTACCC | 84749 |
| rs564483588 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109025173 | GACTTACATGTGTGG[A/C]CCCCTTGGGTTTTTG | 84749 |
| rs564540807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, downstream-variant-500B | USP30, USP30-AS1 | GRCh38.p7 | 12:109051664 | AACCTCCACCACCAC[A/G]GTTCAAGCAATTCTC | 84749 |
| rs564547946 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109060042 | CTCGGAAGCTAAGCC[A/G]GGTAGTGGTTGGCTA | 84749 |
| rs564619938 | in-del | -/TGTC | | | intron-variant | USP30 | GRCh38.p7 | 12:109034107 | AAAAACAGCTCAACG[-/TGTC]TGTCTGAGTCGTTGT | 84749 |
| rs564637047 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109045360 | CAGGTGTTAATGAGA[G/T]CCCAGCTAAAATCAG | 84749 |
| rs564664226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109045986 | TCCAAAATCTATAGA[A/G]TGTGCCAGAAAGCTG | 84749 |
| rs564690258 | snp | A/G | 1.64844e-05 | 0.00287087 | intron-variant | USP30 | GRCh38.p7 | 12:109081303 | AACTAAGCCTAAATC[A/G]TTTCTGGATTTTCTG | 84749 |
| rs564715126 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022659 | CTGGACTTAAAACCC[C/T]GGCAGTCTATCTCCA | 84749 |
| rs564722498 | snp | A/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109087953 | TAACTGCTGATTTAT[A/G]TATTTGCTAAAGGTA | 84749 |
| rs564724954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109030143 | CTACAAAAATCCTGT[C/T]GCCCTGCCCAGCTGT | 84749 |
| rs564857150 | snp | G/T | 0.00953873 | 0.0683987 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109085998 | AAAAAAGTAAAACTG[G/T]ACTGTTGCGTGTGCA | 84749 |
| rs564893317 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109051404 | TGGGATTACAGGCAC[A/G]CGCCACCACACCTGG | 84749 |
| rs564933503 | snp | A/G | | | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022497 | GTGCCAGGCACCCGG[A/G]TATGTACTTCACCAT | 84749 |
| rs564983329 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109060341 | AACTTTTAACAATAA[A/G]CATATATTGCTCTCA | 84749 |
| rs565013995 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109047681 | ATCCTCTGGGCCAGC[C/T]CTCTCCTCTAGTGAC | 84749 |
| rs565023108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109072187 | CTGAGCTTTGTTAAA[A/G]GTTGATTTTTAGTGG | 84749 |
| rs565025781 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109085239 | GTCCAAAATGGAAAT[A/G]ACTTTTAAATTAAAA | 84749 |
| rs565155007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109066404 | AAAAGTAAACCACTC[A/G]GGTGGGTGCAGTGGC | 84749 |
| rs565165564 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109087528 | CGTCCTGCACTCACC[C/T]GATGCAGACCTTGAC | 84749 |
| rs565184300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109036997 | TTTGGCATCTTTTTT[C/T]CTTCAGGTATTTTTT | 84749 |
| rs565275833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109029468 | TCTCTCTGACACTAC[A/G]GGCATATCCCCTGAG | 84749 |
| rs565297564 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109031624 | CAATAGATGAATGGA[A/T]AAACAAAATGTGGTC | 84749 |
| rs565339166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109057487 | GTCTTTCCCAGTGAT[C/T]GTTAAGATAAGAACA | 84749 |
| rs565353893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109029838 | GGCTATGGGTAGGGC[C/T]GGTTCCTAGAAGGTA | 84749 |
| rs565391701 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109071436 | ACCTCTTGCTTGAGG[A/G]TCTTCACTCGTGACA | 84749 |
| rs565423536 | in-del | -/AG | 0.00716266 | 0.059414 | intron-variant | USP30 | GRCh38.p7 | 12:109073888 | CAACATCATACAAAA[-/AG]AGAGAATTGTACAAC | 84749 |
| rs565432299 | snp | A/G/T | 0.00517822 | 0.0506191 | intron-variant | USP30 | GRCh38.p7 | 12:109030330 | GGATTAAACAAGATG[A/G/T]TGGATATTCATGTGC | 84749 |
| rs565440888 | snp | A/G | 4.94295e-05 | 0.00497115 | missense | USP30 | GRCh38.p7 | 12:109085704 | CTGATGGCAGTTGTC[A/G]TCCACCATGGAGACA | 84749 |
| rs565576837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109042727 | ACAACTTCTATTTAA[C/T]GTAGTACTGGAAGTT | 84749 |
| rs565742920 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109051161 | CCCAAAGTGCTGGGA[C/T]TATAGGCATAAGCCA | 84749 |
| rs565837480 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109050780 | TTGGGAGCCCGAGGC[A/G]GATGGATCACGAGGT | 84749 |
| rs565893189 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109071533 | CACATTCACTGTAGG[A/G]TGTCTGCCCGAGGTG | 84749 |
| rs565931318 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109068977 | GCTTCAGAGGATGCA[C/T]TGGGCCAAAGGCTTG | 84749 |
| rs565988220 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088130 | CCTTTCTGTGTTCCC[A/T]GTTGGTAAGGGAAAT | 84749 |
| rs566053091 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109085479 | ATACACAATATACAT[A/G]TACTCATAGAATGTA | 84749 |
| rs566065679 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109066541 | ATACAAAAATTAGTC[A/G]GGCATGGTAGCGCAT | 84749 |
| rs566125943 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109064864 | AAATTTTCCTTTGGG[G/T]GGTAGTTGGTGGGGG | 84749 |
| rs566177193 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109030657 | GAGTCTCACTCTGTC[A/G]CCAGGCTGGAGTGCA | 84749 |
| rs566246395 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109034645 | GTTAGAAACAGTTTA[G/T]AGTGTTGTTCACGTC | 84749 |
| rs566267363 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109079512 | GGGACTACAGGTGTG[G/T]GCCACCACACCCAGC | 84749 |
| rs566283090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109035457 | CAACCTCCGCCTCCC[A/G]GGTTCAAGCGATTCT | 84749 |
| rs566290446 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109069592 | GGACTGTCGAGGGCA[A/G]TGGAGTCGTAGCAGC | 84749 |
| rs566299664 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109078772 | TACTGCTGACAGATA[C/T]ACTTAGATTTCATGT | 84749 |
| rs566323554 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054239 | AGAATACCTTTCACC[A/G]GCTGGGCATGGTGGC | 84749 |
| rs566337561 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109024497 | TCGTGAGCTCAAGCA[A/G]TCAACCTGCCTCGGC | 84749 |
| rs566375859 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109062564 | CAATCTCCTGACCTC[A/G]TGATCCGCCCGCCTT | 84749 |
| rs566381858 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109071026 | GGAAAATAAGCCAGT[C/G]ACAAAGACCAACACT | 84749 |
| rs566396001 | snp | A/C | 0.00199481 | 0.0315187 | upstream-variant-2KB, utr-variant-5-prime | USP30, SVOP | GRCh38.p7 | 12:109021093 | AGAGGAGGCGGAGGG[A/C]AGAGCGAGCTGCGCG | 84749 |
| rs566425638 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109049769 | TGCAGTGAGCCAAGA[C/T]TGCGCCACTGCACTC | 84749 |
| rs566498183 | in-del | -/CCTAAC | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109061257 | GTCCACATGAGTTAT[-/CCTAAC]CCTGACCTCAGCACT | 84749 |
| rs566499725 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109040777 | TGGCTTTTCCCAGAG[A/C]AAGTGTTTCAAGAAA | 84749 |
| rs566506416 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109060423 | TGAGGTATTTTCCCA[C/T]GTGAGCTCTGCTTGA | 84749 |
| rs566554760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109042134 | TAGGTATCTTCATAC[A/G]AGATTGTGACCACAT | 84749 |
| rs566766463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046993 | TTGAGCCACTGCGCC[C/T]GGCCAGCTGGAAGTT | 84749 |
| rs566845801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109026171 | ACCTCCACTTCCCAG[A/G]CTCAAATCATCCTCC | 84749 |
| rs566986602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109026603 | TAGCTTCCTGTAGTA[A/G]ACCGTAGGTGCGCAC | 84749 |
| rs566988383 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109085967 | AGAGCTGATGGCACT[A/G]TCTGCACTGTCCAGG | 84749 |
| rs567096701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053970 | TGTGACCAAGTTGGG[C/T]TCTTAGTTTCTTCTG | 84749 |
| rs567122232 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | USP30 | GRCh38.p7 | 12:109065469 | ACAAAGTGTGAAGGC[A/G]GCTGTCTGGGGACAC | 84749 |
| rs567233552 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109023213 | ATCCTGGTGTCAGGT[A/G]GGGCTCTCTAGGGCT | 84749 |
| rs567240097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109043915 | GAGATATTTGTATAT[A/G]CCCATGTTCATAACA | 84749 |
| rs567276793 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP30 | GRCh38.p7 | 12:109036394 | CAACCTCCACCTCCC[A/G]GGTTCAAGAGATTCT | 84749 |
| rs567339060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109034492 | AACGCTTTGGGAGAC[C/T]GAGGTGGGAGGATCG | 84749 |
| rs567339410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109026668 | GGAAGGAGTCTCACT[A/G]TGTTGCCCAGGCTGG | 84749 |
| rs567413910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109063369 | GCCTCCCAAAGTTCT[A/G]GGATTACAGGCGTGA | 84749 |
| rs567446616 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109049659 | ATCTCTACTAAAAAC[G/T]CTAAAATTAGCCAGG | 84749 |
| rs567469366 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046187 | TCACTGGAACCTCCG[-/C]CCCCCCCGGGTTTAA | 84749 |
| rs567536410 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | USP30 | GRCh38.p7 | 12:109045280 | CACTGCGCCCGCCCA[A/G]ACATCTTTCCAAAGG | 84749 |
| rs567550033 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109077567 | TGTGACTTTGTGGAC[A/T]GCATATAATGGGTCT | 84749 |
| rs567588208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109069683 | ATAGCAGGCAGGGGT[C/T]GGTGCAGACAGTAAG | 84749 |
| rs567649180 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109033701 | TGGGATGGCACTTCC[A/T]TCTAGAGTCACTCCC | 84749 |
| rs567695972 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109078148 | ATAGCTGCACCAGCC[A/T]GGTGCTGTGGCTCAC | 84749 |
| rs567770826 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109070165 | GCAAGAATGCAAGCC[C/G]AGAGGAAAGGTGGGA | 84749 |
| rs567826610 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109045070 | GCAACCTCCGCCTCC[C/T]GGGTTCTAAGCGATT | 84749 |
| rs567831237 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054917 | TTATTATAAAACAGG[G/T]TCAATATTACCACCA | 84749 |
| rs567857013 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109048392 | CGCCTGGCCTGCTTC[A/G]GTATTGTTGGGTTTT | 84749 |
| rs568011522 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109068523 | TCTATACTTTCTTAA[A/T]ATGTATCTCAGTTAA | 84749 |
| rs568111386 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109061777 | AAAGATTAAAGCATT[A/G]CAGAGAAGGCCAAAG | 84749 |
| rs568147665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054190 | GTGAACTCACGTATC[A/G]TGTAAAAGCACAGTG | 84749 |
| rs568218164 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109025496 | TTAGCTGGCCTATGA[A/C]GGATAAGAAAAATAG | 84749 |
| rs568272167 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109066638 | TGCAGTGAGCTGAGA[G/T]CACGCCATTGCACTC | 84749 |
| rs568280076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109031669 | AATATCATTCAGCCA[C/T]ACAAATGAATGACGT | 84749 |
| rs568287766 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109067821 | CTGTTTTTCACTCAG[C/T]GGATGGAAGGTTAGC | 84749 |
| rs568311142 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109029070 | GCTCAGCTATGAATC[A/G]TGTCAAGTTTCCTAC | 84749 |
| rs568366406 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109026729 | CACCTCGGCCTCCCA[A/G]AGTGTTGAGATTACA | 84749 |
| rs568397283 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109060240 | AAAGACTGGACTGAA[A/C]AATGCTGAAATGTTA | 84749 |
| rs568456206 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109058279 | GTATTTTTTAAAAAT[C/G]AAAGATGGAGGCCGG | 84749 |
| rs568468764 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109062173 | CTCCTGGGCTCAGGT[C/G]ATCCACCCGCCTCAG | 84749 |
| rs568558633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109039565 | ACTGATCTAGTTCCC[A/G]AGAAAAAATGTGGGG | 84749 |
| rs568688491 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109026238 | ATGCCATCACACCTT[C/G]CTAATTTTTGTATTT | 84749 |
| rs568720413 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, downstream-variant-500B | USP30, USP30-AS1 | GRCh38.p7 | 12:109051957 | GTTGGAGAGTGCCAT[G/T]CTGGAGACAGACAGA | 84749 |
| rs568785511 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109062530 | AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 84749 |
| rs568874825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046944 | TCAGGTGATCCACCC[A/G]CCTGGGCCTCCCAAA | 84749 |
| rs568911958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055038 | CACACACACAAACAC[A/G]TATGTATGCATGTGT | 84749 |
| rs568982992 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109068698 | TTTTTTAAGGTCCGA[C/G]TTCTCCATCAAGGAC | 84749 |
| rs569046503 | in-del | -/A | 0.0905309 | 0.192535 | intron-variant | USP30 | GRCh38.p7 | 12:109048739 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAC | 84749 |
| rs569070934 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109061918 | ATAGAAATTATATAT[G/T]GTAGGTTTTTTTGTT | 84749 |
| rs569098891 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109057536 | AGTAACAACAGAACA[A/G]TTGTTTTCTTCTGTT | 84749 |
| rs569145278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052676 | GCCTCCGGTGCGGCT[A/G]CAATGCTGAGCTCCC | 84749 |
| rs569170993 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109039993 | AGATGACTTGGGGTG[A/T]TATATGATATAAATA | 84749 |
| rs569184001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053108 | TGCCAAGACCCCTCA[A/G]TCCTTCTAGTATACC | 84749 |
| rs569250906 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109031794 | TATGAGGTCTCAAAA[G/T]TAGTCACTCATAGAA | 84749 |
| rs569305904 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109060399 | ACATTCAGCTAAATC[A/G]TGCTTCACTGAGGTA | 84749 |
| rs569320875 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109072940 | CATTCCCAGGTCAGG[C/T]AGTGAATAAGAAGCA | 84749 |
| rs569325816 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109024117 | TTCCGTGCTTGCATT[G/T]CCTCATCAGAAATAC | 84749 |
| rs569325980 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109031007 | TCAGGGGATGCTGAG[A/C]AAAGGGTATACCAGA | 84749 |
| rs569363473 | snp | C/T | | | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109087049 | CTAGTATTGTCATGT[C/T]GCTCTAGGTCCATAT | 84749 |
| rs569639334 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109041712 | ATAAATTAGATGATG[C/T]CTATTCCATGGCAAA | 84749 |
| rs569662110 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109073271 | CTCCTATGAAGGAAT[A/G]GGATGTCTTTTGGAT | 84749 |
| rs569698854 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109074084 | ACCTCTGTCTCTATG[C/G]ATTTGCATATTCTGG | 84749 |
| rs569795991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109045071 | CAACCTCCGCCTCCC[A/G]GGTTCTAAGCGATTC | 84749 |
| rs569834890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109037772 | TTGCCAAGGAGTGCC[A/G]TGTGTGTTGGGGTAC | 84749 |
| rs569841724 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB, downstream-variant-500B | USP30, USP30-AS1 | GRCh38.p7 | 12:109051771 | GATGGGGTTTCACCA[C/T]GTTGGCCAAGCTGGT | 84749 |
| rs570016821 | snp | A/T | 0.000399281 | 0.0141238 | stop-gained, intron-variant | USP30 | GRCh38.p7 | 12:109058105 | CTCTTGCACCTTCTG[A/T]AAGGTATCTAGATGG | 84749 |
| rs570114339 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | USP30 | GRCh38.p7 | 12:109058631 | TTGTCAAGTTAATAA[A/C]AGCTTTTTAAGGAAG | 84749 |
| rs570137645 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109063042 | TTAATGTCTTCAGGG[G/T]TCATCCATGTTATAC | 84749 |
| rs570151449 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109051366 | GGTTCTAGCGATTCT[C/T]CCGCCTCAGCCTCCC | 84749 |
| rs570232109 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109066378 | ATTAGGCCTGATTCT[A/C]CCTGTGATTGAAAAG | 84749 |
| rs570276557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109028973 | AAATGTCCTTGAGAT[C/T]TGAAAATATTGATGT | 84749 |
| rs570314544 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022152 | GTGAGCCATTGCGCC[C/T]GGCCTCAGGGTATTT | 84749 |
| rs570450088 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109069294 | CTTCAAGCCTGGGCC[C/T]AGATGCCTGGTGTGT | 84749 |
| rs570456562 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109060500 | ACTTGGGAATAATTT[A/C]TTTTACTATCCTGTT | 84749 |
| rs570469803 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109060871 | GGCTGCTCTCGAACT[C/T]CTGACCTCAAGTGGT | 84749 |
| rs570631804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109038738 | ATTCCTGCTAGCAAC[A/G]TATGATATCCAGTTG | 84749 |
| rs570632723 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109030640 | GTTTGTTTTTTGAGA[C/G]GGAGTCTCACTCTGT | 84749 |
| rs570650676 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109031133 | GCCATCTTAATATAG[G/T]ATATTTTATAGAACT | 84749 |
| rs570668131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109039425 | TTGTGTTCTAGTCAT[C/T]TGACCTTAGATAAAG | 84749 |
| rs570703194 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109072550 | CCCAGCCCAGCTGAC[G/T]TTTCTTGAAACTGGC | 84749 |
| rs570712749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109059333 | CTGAGTAGCTGGGAT[A/G]ACAGGTCTGTGCCAC | 84749 |
| rs570740401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109066006 | CCTGTAATCCCAGCA[C/T]GTTGGGAGGCCAAGG | 84749 |
| rs570763201 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109074135 | CATGTAATGTGTGGC[G/T]TTTTGTGTCTGGCTT | 84749 |
| rs570779234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109051450 | TTTAGTAGAGACGGG[A/G]TTTCACCATATTGGC | 84749 |
| rs570798488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, downstream-variant-500B | USP30, USP30-AS1 | GRCh38.p7 | 12:109051895 | TTTTCACTTTAATGT[A/G]GCTACTGGAAAATGT | 84749 |
| rs570873914 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109023199 | CCCCTTTTCCCTCAA[C/T]CCTGGTGTCAGGTGG | 84749 |
| rs570903551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, nc-transcript-variant | USP30, USP30-AS1 | GRCh38.p7 | 12:109052527 | GCAGCTACTTCCGGT[C/T]CCCCTGGGAGCTGTC | 84749 |
| rs570910681 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | USP30 | GRCh38.p7 | 12:109041844 | GAAGTGGGGTTTTAG[G/T]ATCCCTCTGTCAATT | 84749 |
| rs570936775 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109045661 | AGGAGGGGCTGTTGG[A/G]AGGATGAAACAGGGC | 84749 |
| rs570994056 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109062620 | GGCTTGAGCCACCGC[A/G]CCCAGCCTTTTTTTT | 84749 |
| rs571120442 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109023930 | GATCACCACCGCGAC[A/T]GGCCAATCAGTATTT | 84749 |
| rs571139273 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109066960 | TTTGAAGATACAGGA[A/G]TCGGTTACTTCATTT | 84749 |
| rs571149889 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109049974 | AATGCAGTATCTTCG[A/C]AGCACAATAAAGTGA | 84749 |
| rs571186021 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109050774 | AACACTTTGGGAGCC[A/C/T]GAGGCGGATGGATCA | 84749 |
| rs571199523 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109086990 | TCACGAAAAGGAGAA[A/G]GCAGCTTTTGACTTT | 84749 |
| rs571232166 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109036484 | TGTATTTTGGATAGA[C/G]ATGGGGTTTCACCAT | 84749 |
| rs571291937 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | USP30 | GRCh38.p7 | 12:109029719 | GAGGTTAGAAAGGGA[A/C]CTGGAACAAAGTGGC | 84749 |
| rs571296985 | in-del | -/TATGA | 0.00795532 | 0.062565 | intron-variant | USP30 | GRCh38.p7 | 12:109071270 | TAAGATGATAAATGT[-/TATGA]TATGTGTATTTTACC | 84749 |
| rs571318923 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109029047 | GGCATCTTTACAACT[C/T]CTGCTCAGCTCAGCT | 84749 |
| rs571329808 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109049047 | GGTCCCCTTGGCCAA[C/G]AGGGGGCCCATTCAG | 84749 |
| rs571411449 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109078208 | AGACGAGTGGATCAC[A/G]AGGTCAGGAGTTCAA | 84749 |
| rs571441531 | in-del | -/T | 0.276534 | 0.248588 | intron-variant | USP30 | GRCh38.p7 | 12:109048079 | TAATAGAATGCCTAC[-/T]TTTTTTTTTTTTTTT | 84749 |
| rs571575382 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109028060 | CCTCAACACTTGTTG[A/T]TAATAGCCATCCCAG | 84749 |
| rs571609039 | in-del | -/T | 0.00716266 | 0.059414 | intron-variant | USP30 | GRCh38.p7 | 12:109057050 | AGCGGCATAATTGTC[-/T]TAAGAAGTGTTCTCA | 84749 |
| rs571642791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109027347 | GCAGTGATGCAATCA[C/T]GGCTCACTGCAACCT | 84749 |
| rs571655903 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109078682 | CTTGTTCTCAGTCTT[A/T]CTTGTAGATCAAAAT | 84749 |
| rs571698708 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109070857 | TAATAGCAGCATGTT[C/T]GCAATAGCCAAGGGG | 84749 |
| rs571726191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109084575 | GCACAGGACAGCCCC[C/T]GCAACAAAGAATGAT | 84749 |
| rs571761513 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109080921 | AGGTTCTTGTAAGCG[C/T]GCTCTGCGATGTTTA | 84749 |
| rs571831571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109066122 | CTGAGCACAAGGACA[C/T]GTGCCTGTAGTCCCA | 84749 |
| rs571833166 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109049051 | CCCTTGGCCAAGAGG[A/G]GGCCCATTCAGTCAG | 84749 |
| rs571875623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109043484 | TTGAATGGGAAAAGG[A/G]CAGTCTTCATCAAAT | 84749 |
| rs571880788 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109071393 | TGAAGGCAGCCACCT[A/G]GCTTTCTCTCCTGCT | 84749 |
| rs571881992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109042065 | GATAACCCAGAGTGA[C/T]CACTTAAGAGGCATA | 84749 |
| rs571944624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109071925 | TGATTCATTGCTGCA[A/G]TTTGTGTTGGCTTTG | 84749 |
| rs571962903 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022355 | AGGAAACATTTTTTT[C/T]TTTTTTTCTTTAATT | 84749 |
| rs572016808 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109067487 | TTAGTTGTTATGCTG[A/G]TGAATTTAATAATTG | 84749 |
| rs572202517 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109042350 | CTGTCCTCAGTCATA[C/T]GGTTCTTTTCCCAAA | 84749 |
| rs572298023 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109028536 | AGACTGGAGTGCAAT[G/T]GTGTGGTCTCAGCTC | 84749 |
| rs572334894 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109021405 | ACTGGGGGTATGACA[C/G]AACAAATTCGACCTG | 84749 |
| rs572419048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109067274 | ACCCACCACCACGCC[C/T]GGCTAATTTTTTTTT | 84749 |
| rs572431098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109050033 | GGGCACGGTGGCTCA[C/T]ACCTGTAATCCCAGA | 84749 |
| rs572449472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109049536 | GAAAAACTTTGGGAC[C/T]AGGCACGGTGGCTCA | 84749 |
| rs572584150 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109026084 | ATTTTTTAATTAAAA[A/T]AAATTTTTTGAAACA | 84749 |
| rs572660876 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109062082 | TGGGACTACAGGTGC[A/G]TGCTGCCACACCTGG | 84749 |
| rs572797143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109063442 | TATATGCAGCATTTT[A/G]TTTGTCCCTCTGTCA | 84749 |
| rs572844223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109041081 | GTTTCCTCATCAGTC[A/G]ACTGAGCTGGCCTCT | 84749 |
| rs572863239 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109047014 | GCTGGAAGTTTTGAT[C/T]CAGACCTCAAACCAA | 84749 |
| rs572865698 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109084628 | TGCTGTTGAGAAACC[C/T]TGGTTTAGGTCAAAA | 84749 |
| rs572895896 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109067468 | TACTGTGCAAGTTTT[C/G]TGGTTAGTTGTTATG | 84749 |
| rs572910345 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109072024 | CCCTCATTTCCCTGT[-/A]AACAGTATAAATATC | 84749 |
| rs572910537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053649 | TCCTGTCCAGTGCCC[C/T]CATTCCGTAGATAGG | 84749 |
| rs572999963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109047359 | TGGTCAGCGGATCAA[C/T]GGGAAAAAACAAGAG | 84749 |
| rs573006554 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109051431 | TGGCTGATTTTTGTA[-/T]TTTTTTAGTAGAGAC | 84749 |
| rs573019620 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109061366 | TCATTTCTCTGCTTC[C/T]GCTTTCCAATGTCTC | 84749 |
| rs573038271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054318 | TTGAGCTCAGGAGTT[C/T]GAGACCAGCCTGGGC | 84749 |
| rs573041481 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109048694 | GTAGTGAGCCAAGAT[C/T]GCCCTACTGCACTCC | 84749 |
| rs573046144 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109079686 | CTTTTTTCATCTCCA[A/G]TCTCTGTTTGCCTAT | 84749 |
| rs573056526 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046620 | GACAATTAAACTTAA[C/G]CATCACACCCAGGGA | 84749 |
| rs573070375 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109039005 | ACATATTCCGGATAC[A/G]AGTCTTTGTTAGATA | 84749 |
| rs573145681 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109039693 | TCAGCTCACTGCAAC[C/T]TCCACCTCCCAGGTT | 84749 |
| rs573183804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109040174 | GTCTACATATGGCAA[A/G]CAAAAAAAAAATTTA | 84749 |
| rs573189225 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109075379 | TTTCAGACAGAGTCT[C/T]GCTCTGCTGCACCCA | 84749 |
| rs573199345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109025696 | TTTTTTTTTTTGACA[A/G]GGTCTTGCTCTGTCA | 84749 |
| rs573351764 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109028587 | GGTTCAGGCAATTAT[A/C]CTGCCTCAGCCTTCT | 84749 |
| rs573370324 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109078340 | GAGGCAGGAGAATGG[A/C]TTGAACCCAGGAGGC | 84749 |
| rs573432696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109082488 | CTGTTTCTGTTATTT[A/G]ATGACTAAGAGGGAT | 84749 |
| rs573463845 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055433 | TTTGAGGCAGAGTCT[C/T]GCTCAGTCACCCAGG | 84749 |
| rs573469836 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109074528 | TTTCTTCACAGCCTC[A/C]CCCACATTTTGATGT | 84749 |
| rs573659050 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109074968 | TGAGATCAGGTGGTG[G/T]TTATCTTTCTATATC | 84749 |
| rs573680562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109034815 | GTATTGTTAAGTGCA[C/T]GTATGATTACAATTG | 84749 |
| rs573682653 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109027005 | CTTCTGTAACCCTGA[G/T]TACTTCCCAAAGGCC | 84749 |
| rs573712472 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109078781 | CAGATACACTTAGAT[G/T]TCATGTATATGAAAA | 84749 |
| rs573724578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109062180 | GCTCAGGTGATCCAC[C/T]CGCCTCAGCCTCCCG | 84749 |
| rs573799507 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP30 | GRCh38.p7 | 12:109024637 | GCATTTTTTTTTTCC[C/T]GAGACCGAGTCTCGC | 84749 |
| rs573820117 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109062600 | CCCAAAGTGCTGGGA[C/T]TACAGGCTTGAGCCA | 84749 |
| rs573820263 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054336 | GACCAGCCTGGGCAA[C/T]GTAGTGAGACCCTGT | 84749 |
| rs573829446 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109048672 | TTGAACCTGGGAGGT[A/G]GAGGTTGTAGTGAGC | 84749 |
| rs573854738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109041685 | TATGTGAAGTATGAA[C/T]TTATCAATCATATAA | 84749 |
| rs573983367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109032666 | GTGGAGGGGGAAATG[A/G]AGATTGACTGCTAAT | 84749 |
| rs573999327 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109043684 | GTGATTTCTTGGATA[C/T]GACACCAAAGACACA | 84749 |
| rs574020154 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109026228 | CTGCAGGCGCATGCC[A/T]TCACACCTTGCTAAT | 84749 |
| rs574051477 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109059600 | CTCACTGCAACCTCC[A/G]CCTCCCGGGTTCAAG | 84749 |
| rs574067611 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109039678 | TTCAGTGGCACGATC[G/T]CAGCTCACTGCAACC | 84749 |
| rs574216977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109075742 | TGATGATTAGTGATA[C/T]TGAGTGCCTTTTCAT | 84749 |
| rs574354376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109083795 | AGGATTGTCTCACAC[C/T]CCATACTTTCCTATT | 84749 |
| rs574367710 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109028016 | ATTCCCACCAGCAAT[A/G]CACAAGGATTCCAAT | 84749 |
| rs574427147 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109039773 | CCGCCACCACACCCA[C/G]TGAATTTTTGCATTT | 84749 |
| rs574446986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052783 | TTTTGGGGGGCGGGG[C/T]TGCCGAAGAGGCCGG | 84749 |
| rs574472096 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109081093 | AATCCCAAAATTATT[C/G]CTGGGTCAGATATTT | 84749 |
| rs574562914 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | USP30 | GRCh38.p7 | 12:109081624 | ACGCACGCATGCGCG[C/T]ACACACACACACACA | 84749 |
| rs574571291 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109074295 | GGCATTTGGATTGTT[A/C]ACACTTTTTGGCCAT | 84749 |
| rs574652337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109058949 | AGTGCCACTTTTCTG[A/G]AAAGCAGTTTGGAAC | 84749 |
| rs574700109 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109078577 | GCATGCCAGCCTGGG[C/T]GACAAAGCGAGACTC | 84749 |
| rs574747353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109045729 | ACAAGTTTTGGCAGG[C/T]GGTTGCAATCAGTAT | 84749 |
| rs574850813 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109038169 | ATGCTCTCCCTCCCC[C/T]GACCCCTCCAAAGGC | 84749 |
| rs574867674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109024367 | GGCTCAAGCCATCCT[C/T]CCACCTCAGCCTCCC | 84749 |
| rs574887743 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109029984 | CACTCTACATTCTTA[A/T]ACAAGCAAATAGTTT | 84749 |
| rs574889764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109038857 | TTTTGTATCCCTGAT[A/G]ACTAGTGATGTTGAC | 84749 |
| rs574980406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109051528 | CCCACCCCCCGGCCT[C/T]CCAAAGTGCTGGGAT | 84749 |
| rs575010348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109045259 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCGCCC | 84749 |
| rs575046741 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109087457 | ACAGAATATTCTGTG[A/C]AGGCTCTCCAGGCTC | 84749 |
| rs575057952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109055995 | AAAGGAGTGAGCCAA[A/G]CAGTGATCTGGGGGA | 84749 |
| rs575150149 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109056131 | ACTTCAGTTTTTCCT[A/C]AGAGTGAGAAGTAGC | 84749 |
| rs575197917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109040472 | CCCCAAAACTTAGCA[C/T]CTTTAAAAAAATTAA | 84749 |
| rs575201649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109083234 | AGATTTCTTAGAAGA[A/G]GTTAAAATTATGTAG | 84749 |
| rs575260178 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109084348 | CTACCCATAAACATG[A/T]ATGAATGCTATTACA | 84749 |
| rs575284657 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109041009 | GAACCAGATTCTCTA[A/C]CAGGAAATGGGGTGT | 84749 |
| rs575337464 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109083956 | GGGGACAGACTCTGG[G/T]TCAGTCCTTGGCCCT | 84749 |
| rs575338858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109060638 | TTTAAATGCGAAAAT[A/G]GAAAAACTGTTCTTG | 84749 |
| rs575386379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, nc-transcript-variant | USP30, USP30-AS1 | GRCh38.p7 | 12:109052143 | ATACCTGGCACCCAA[A/G]TAAACAATAAGTTTG | 84749 |
| rs575538912 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052817 | CAGGGTCCCCAGCTT[C/G]GGCCCGTGACGGCTT | 84749 |
| rs575554509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109033651 | TGGGGGAATAAAACA[C/T]TGATGGAAAGTCCCT | 84749 |
| rs575568721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109039660 | CCTGTCACCAGGCTG[C/T]AGTTCAGTGGCACGA | 84749 |
| rs575583355 | snp | A/G | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | USP30, USP30-AS1 | GRCh38.p7 | 12:109052412 | ATCTGAAAACCAAGC[A/G]GCCCCAGGCAACTGA | 84749 |
| rs575596682 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB, nc-transcript-variant | USP30, USP30-AS1 | GRCh38.p7 | 12:109052466 | GGGCCTGTTGCTAAG[A/G]GAAAAGAAAGAAAGG | 84749 |
| rs575624515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053595 | CTGGAGCAGGTTTAA[A/G]GAGCTTATTATCCCA | 84749 |
| rs575655797 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109067410 | GCATGAGCCACCACA[A/C]CCAGCCTGCGGTCTT | 84749 |
| rs575674188 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109050270 | CTGCACTCCAGCCTG[A/G]GCCACAGAGCGAGCC | 84749 |
| rs575718788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109024407 | GGATTACAGGTGTGC[A/G]CCACCATGCCAGGCT | 84749 |
| rs575937617 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109066326 | CCAATCCTTGGTCTA[G/T]AAGTAATTATAATAT | 84749 |
| rs576100716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109059617 | CTCCCGGGTTCAAGC[A/G]ATTCTTCTGCTTCAG | 84749 |
| rs576202577 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109067233 | ATTCTCCTGCCTCAG[C/T]CTCCCGAGTACCTGG | 84749 |
| rs576249128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109072104 | AAGAAATATGTTTCT[A/G]TTGCATTTGATGAAA | 84749 |
| rs576284399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109080040 | TCTGTCTCCCCTACA[C/T]TGGGCAGCAAAATCT | 84749 |
| rs576287710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109065263 | ACTGGTCTAGTGTAA[C/T]ATGCTGGGAAGGAGG | 84749 |
| rs576372996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109080832 | ATTCAGTACGGTAAC[A/G]TGTTATACAGGTTGG | 84749 |
| rs576409611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109072776 | TGTGTAGTAATAGGA[A/G]CAAATATTTTTTGAG | 84749 |
| rs576432030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109043564 | TACCTAACAACACAT[A/G]CAAAAGTTAATTCAA | 84749 |
| rs576447581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109044508 | CAGGCACAAAGGCTC[A/G]TGTCTGTAGTCCTAG | 84749 |
| rs576468639 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109035905 | CAATGACTTATGTCT[A/G]TAATCCTAGCACTTT | 84749 |
| rs576521169 | snp | A/G | 8.26098e-05 | 0.00642636 | synonymous-codon | USP30 | GRCh38.p7 | 12:109085026 | ATCTTTATTGCCAAC[A/G]CTGTCAGCGCCGATG | 84749 |
| rs576544053 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109050834 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 84749 |
| rs576555848 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109086180 | GTCCGGAGTGTCTTT[C/T]TACTCATCTGATACA | 84749 |
| rs576588474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109064389 | CCTGCCACAGCTTCC[C/T]AAGTATTTAGGACAA | 84749 |
| rs576634508 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109023494 | CAGGAAGCAGAGGTT[A/G]CAATGAGCTGAGATC | 84749 |
| rs576703549 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109059052 | GAAAATGGTTAGAAA[C/T]GTAGATTGTGACTTA | 84749 |
| rs576722626 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109059679 | CCACCACGCCCGGCT[A/G]ATGTTTGTATTTTTA | 84749 |
| rs576722879 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109066687 | ACGACTCTGTTTCAA[A/G]AAAAAAGAAAAGTAC | 84749 |
| rs576735484 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109056426 | TCAAACTCTGGGGTT[C/G]AAAGGATCCTCCTGC | 84749 |
| rs576857338 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109064309 | TTGTTCTGTTGCCCA[-/G]ACTGGAGTGCAGTGA | 84749 |
| rs576888500 | snp | A/G | 0.000141478 | 0.00840945 | intron-variant, missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052708 | GGCCGAGGCGGCGAT[A/G]ACCGCGGCCGACAGG | 84749 |
| rs577060731 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP30 | GRCh38.p7 | 12:109083545 | CTCATTTAAGCCGGG[C/T]AGCTATTATCGCCGG | 84749 |
| rs577061523 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109024192 | CAAAGATAAAATGGA[G/T]GTGAAGGACCACACA | 84749 |
| rs577088317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109059029 | CCATGTCTGGGAGTC[C/T]GCCTTATGAAAATGG | 84749 |
| rs577141492 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109066464 | GTTGAGGTGGGCGAT[A/C]ATGAGGTTAGGAGTT | 84749 |
| rs577143436 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109073351 | TCTTAAGAGGTAGTT[G/T]CTACCACATGCTAGA | 84749 |
| rs577212632 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109037156 | TCTCAATGGAACTAT[A/C]TTCATGTTCATTGAT | 84749 |
| rs577232573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109066732 | CCTTTAGGCTGCTGC[A/G]TATAGCTTGATGCTT | 84749 |
| rs577242429 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109080174 | TTTAGGTATAAACTT[A/T]GGGGCTCATCCCCTC | 84749 |
| rs577360681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109057511 | AAGAACAGAATCATT[A/G]TCCTGGGGAAGTAAC | 84749 |
| rs577376329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109041753 | AAAGAATTTATCATG[A/G]CATTCCTTGAAGAGC | 84749 |
| rs577396540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109058289 | AAAATCAAAGATGGA[A/G]GCCGGGTGCAGTGGC | 84749 |
| rs577452748 | snp | G/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109087897 | AAAGTAAGTAGCTTC[G/T]TTTGGGAAAAACCTA | 84749 |
| rs577461613 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109042423 | TTATAAATGCCTAAT[A/C]TTTTATTCTCTCACA | 84749 |
| rs577474755 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109056015 | GATCTGGGGGAAGAG[C/T]ATTCTGAGCAGAGGG | 84749 |
| rs577534914 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109025207 | CCTTGAATTTGGCCC[A/G]GCATCCCAGGGTTTC | 84749 |
| rs577535374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109027742 | TTCTTTTATATGACT[A/G]AATAATATTTCTTTG | 84749 |
| rs577629769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109050898 | TGTAATCCCAGCTAC[C/T]CAGGAGGCTGAGGCA | 84749 |
| rs577660180 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052822 | TCCCCAGCTTGGGCC[C/G]GTGACGGCTTTTTCA | 84749 |
| rs577731581 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109048747 | TCTGTCTCAAAAAAA[A/C]AAAAAACAAAAAAAG | 84749 |
| rs577812574 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109021395 | TGTAATAGGCACTGG[A/G]GGTATGACAGAACAA | 84749 |
| rs577851233 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109034927 | TTTTGTCTGATATTA[C/G]TGTAATTACTTCAGC | 84749 |
| rs577902453 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109042841 | TGATATGATTTCATA[C/T]GCAGAAAACCTTAAA | 84749 |
| rs577983594 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109070502 | CCAGGGGCCGGGACA[C/T]TGTGAATGTTGGGGG | 84749 |
| rs578062494 | in-del | -/TTTAT | | | intron-variant | USP30 | GRCh38.p7 | 12:109035346 | ATTTCAATTTGTTTA[-/TTTAT]TTTATTTTATTTTAT | 84749 |
| rs578189782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109062272 | GTGATTTACATGGCC[A/G]AATATAATACATTAG | 84749 |
| rs578200775 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP30 | GRCh38.p7 | 12:109076837 | CCCAGGTTCACGCCA[C/T]TCTCCTGCCTCAGCC | 84749 |
| rs745350092 | snp | A/G | 1.64863e-05 | 0.00287104 | synonymous-codon, missense, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088416 | GAAGACAAAGTCTCT[A/G]CAGGCACCGAAGGAG | 84749 |
| rs745382367 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109044531 | AGTCCTAGCTACTCG[C/G]GAGGCTAGGGTGGAA | 84749 |
| rs745397830 | snp | C/T | 1.72207e-05 | 0.00293429 | intron-variant | USP30 | GRCh38.p7 | 12:109057892 | TGATCAAATGTGATA[C/T]ACTGTTCTCTTCTTC | 84749 |
| rs745406073 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109058708 | CTGGTTTCAAAAACA[C/T]TAAAGTAAAAAAAAA | 84749 |
| rs745408997 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109042867 | TTAAAGAGTCCAGAA[A/T]AAAGCTGTTAGAACT | 84749 |
| rs745453077 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109065781 | AAAGGTCAGGAAGCA[A/G]TGGCCATGCGCCAGA | 84749 |
| rs745479131 | snp | A/C | 1.69983e-05 | 0.00291528 | synonymous-codon | USP30 | GRCh38.p7 | 12:109083052 | GGATGGGCCGGGAGC[A/C]CCCACACCAGGTGTG | 84749 |
| rs745618557 | snp | C/G | 3.29457e-05 | 0.00405854 | missense | USP30 | GRCh38.p7 | 12:109085741 | CTGGACACTTTGTCA[C/G]TTACCGACGGTCCCC | 84749 |
| rs745643455 | in-del | -/T | 1.64741e-05 | 0.00286998 | frameshift-variant, intron-variant | USP30 | GRCh38.p7 | 12:109057999 | AGGCCTGTCTGCCTG[-/T]CCTGCTTTCATCAGG | 84749 |
| rs745682497 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109030976 | TACATCTTAAATATA[C/T]ACAGTATTTTTAAAA | 84749 |
| rs745704932 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109066671 | CCCTGGGCGACAGAG[C/T]ACGACTCTGTTTCAA | 84749 |
| rs745771980 | snp | C/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109087988 | TGTATCTGCTGTGTA[C/T]TATAGCAATAAAATA | 84749 |
| rs745797759 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109037679 | TGAAAACTCAGATAG[A/C]TTAGTGGTCAGCTAA | 84749 |
| rs745821878 | in-del | -/TTGTT | | | intron-variant | USP30 | GRCh38.p7 | 12:109056197 | TTGTTGTTGTTGTTG[-/TTGTT]GTTTTTTATGAGACT | 84749 |
| rs745902805 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109074248 | TTGCATTACATGGAT[A/C]TACAACATTTTTATC | 84749 |
| rs745911042 | snp | C/T | 4.96907e-05 | 0.00498426 | synonymous-codon | USP30 | GRCh38.p7 | 12:109082686 | CAAGGGAACGTTGAA[C/T]GGGGAAAAGGTGGAA | 84749 |
| rs745912345 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109025868 | AATTTTTGTATTTTT[C/T]GTAGAGATGGAGTTT | 84749 |
| rs745958748 | snp | A/G | 3.02101e-05 | 0.0038864 | intron-variant, missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052724 | ACCGCGGCCGACAGG[A/G]CCATCCAGCGCTTCC | 84749 |
| rs745964573 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109024724 | TCCCAGGTTCATGCC[A/G]TTCTCCTGCCTCAGC | 84749 |
| rs745994161 | snp | A/C | 2.29508e-05 | 0.00338746 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109085969 | AGCTGATGGCACTGT[A/C]TGCACTGTCCAGGAA | 84749 |
| rs746020241 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109062902 | TTGGTAACCACTGCC[C/G]TACTTTCTCTCTCTT | 84749 |
| rs746046747 | snp | G/T | 1.65091e-05 | 0.00287303 | intron-variant | USP30 | GRCh38.p7 | 12:109067489 | AGTTGTTATGCTGAT[G/T]AATTTAATAATTGTC | 84749 |
| rs746062009 | snp | A/G | 1.6806e-05 | 0.00289875 | intron-variant | USP30 | GRCh38.p7 | 12:109082805 | TGTATCCTGCCCCTG[A/G]AACAACTCGGTTCTC | 84749 |
| rs746200277 | in-del | -/TT | | | intron-variant | USP30 | GRCh38.p7 | 12:109075842 | TCATGTTACTTTTTC[-/TT]TTTTTTTTTTTTTTT | 84749 |
| rs746234543 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109064422 | GGTGTGCACCCATCA[C/G]CCCCGGCTAATTTTT | 84749 |
| rs746248311 | snp | C/T | 1.83421e-05 | 0.00302832 | intron-variant, missense | USP30 | GRCh38.p7 | 12:109083087 | CGCGAGGAGCCGATG[C/T]AGCAGGAATTTTCAG | 84749 |
| rs746254280 | snp | C/T | | | utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109047665 | TTGCAAACTAGGGTC[C/T]ATCCTCTGGGCCAGC | 84749 |
| rs746322385 | snp | C/T | 0.000100032 | 0.00707148 | synonymous-codon | USP30 | GRCh38.p7 | 12:109085880 | GCTGTTCTACGAGCG[C/T]GTCCTTTCCAGGATG | 84749 |
| rs746369212 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109034088 | CTAAGGAAAAGCTCT[C/G]AAACAAAAACAGCTC | 84749 |
| rs746398666 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109032780 | AAACCCCTATTAAAT[G/T]GCACACTTTAAAGGC | 84749 |
| rs746415469 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109048832 | GTAACGCAATCCTTG[C/T]TTGGCATGACCTTAG | 84749 |
| rs746424606 | snp | C/G | 1.77391e-05 | 0.00297813 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052652 | CGGTAGCGGAGGAGA[C/G]GGTTTCAGGCCTCCG | 84749 |
| rs746495911 | snp | A/G | 0.000135311 | 0.0082242 | intron-variant, synonymous-codon | USP30 | GRCh38.p7 | 12:109083112 | TTTCAGCACAGAGAA[A/G]AGCAGTTTGGCATCA | 84749 |
| rs746528855 | snp | C/T | | | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109021837 | GGTGGAGGCCAAGCC[C/T]GGGTATTTTTTATTT | 84749 |
| rs746551776 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109071229 | CAACAACATGAATGT[A/G]CTTAATGCCACAGAA | 84749 |
| rs746553406 | snp | C/T | 3.45572e-05 | 0.00415661 | intron-variant | USP30 | GRCh38.p7 | 12:109058143 | AAGGGAATTATGTAC[C/T]TTTTCAAAGAAGTCC | 84749 |
| rs746589142 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109077858 | GTGAGAGATTACGTT[A/G]TGCAGTTTTACCTTA | 84749 |
| rs746591157 | snp | A/G | 3.30808e-05 | 0.00406686 | missense | USP30 | GRCh38.p7 | 12:109085000 | ATTTTTATGAATGGC[A/G]CCTGCTCCCCATCTT | 84749 |
| rs746606649 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109039091 | GAAAAGAAAAATTTT[A/T]AAATTTTGATTAGAT | 84749 |
| rs746622123 | snp | C/T | 1.6516e-05 | 0.00287362 | intron-variant | USP30 | GRCh38.p7 | 12:109072300 | TTTTTTTTTCTCCCC[C/T]ACAGCAGCAGTCAGA | 84749 |
| rs746723445 | in-del | -/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109063878 | TTTTGAATTGGGTTT[-/C]TTTTTTTTTTTTTTT | 84749 |
| rs746770753 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | USP30 | GRCh38.p7 | 12:109081985 | TCATCTCATCAGAAT[C/T]AGTGCGGGATGTTGT | 84749 |
| rs746810281 | snp | C/T | 1.65894e-05 | 0.00288 | synonymous-codon | USP30 | GRCh38.p7 | 12:109085871 | CGCCTACCTGCTGTT[C/T]TACGAGCGCGTCCTT | 84749 |
| rs746810388 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109028402 | GGAAGCTTAGAGTCA[C/T]GATGGAAGGTGAAGG | 84749 |
| rs746826909 | snp | A/C | 1.64876e-05 | 0.00287116 | intron-variant | USP30 | GRCh38.p7 | 12:109081441 | GTTTCAGAAACATTT[A/C]AATCTGAAAGGGCTT | 84749 |
| rs746831320 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109044176 | AGTTGAATAAATAGA[C/G]ACAAAATGTAGAATA | 84749 |
| rs746852377 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109066552 | AGTCGGGCATGGTAG[C/G]GCATGCCTTGTAATC | 84749 |
| rs746964786 | snp | C/T | 3.29484e-05 | 0.00405871 | missense, intron-variant | USP30 | GRCh38.p7 | 12:109058000 | GGCCTGTCTGCCTGT[C/T]CTGCTTTCATCAGGT | 84749 |
| rs746998882 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109065914 | TGCTTTTGTGCTGCA[A/G]TGGCAGAGTTGAGTA | 84749 |
| rs747041993 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109062844 | CCCGTACTGAAACTG[C/T]ACCCATGAAACAGTA | 84749 |
| rs747046778 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109075409 | AAACTAGAGTGCAGT[A/G]GTGCCATCTTGGCTC | 84749 |
| rs747079580 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109035881 | TACAAAAAATACATG[G/T]GCCAGGCACAATGAC | 84749 |
| rs747113413 | snp | C/T | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | USP30, USP30-AS1 | GRCh38.p7 | 12:109052264 | CTCTGGCCACAATAA[C/T]AACTAATTATAGCAG | 84749 |
| rs747167750 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109073918 | ACTGTCACCCCAATC[C/T]ATTTTATTTTATTTT | 84749 |
| rs747244416 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109024667 | CTCTGTCTCCCAGGC[G/T]GGAGTGCAGTGGCGC | 84749 |
| rs747270949 | in-del | -/TT | 3.32375e-05 | 0.00407647 | intron-variant | USP30 | GRCh38.p7 | 12:109085621 | TTTGCCTATAAAGTC[-/TT]TTTGTTAAAATTGTA | 84749 |
| rs747296705 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109072479 | GTGATGTGCTTGCAA[A/G]GGAACTTGTATTTTG | 84749 |
| rs747342949 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109025600 | AAAACTAGCCATATG[A/G]GTATCTCATATAGAA | 84749 |
| rs747352499 | snp | A/T | 2.06768e-05 | 0.00321527 | downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088169 | CCTCTTAGAGTCGAG[A/T]GGGAAAGAGAAAAGA | 84749 |
| rs747361816 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109060386 | TTGGATTTAAAAAAC[A/G]TTCAGCTAAATCGTG | 84749 |
| rs747366063 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109058945 | ACTTAGTGCCACTTT[C/T]CTGGAAAGCAGTTTG | 84749 |
| rs747378346 | snp | C/G | 5.60099e-05 | 0.00529167 | intron-variant, missense, utr-variant-5-prime, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052748 | CGCTTCCTGCGGACC[C/G]GGGCGGCCGTCAGGT | 84749 |
| rs747392655 | snp | A/G | 9.53971e-05 | 0.00690575 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052659 | GGAGGAGACGGTTTC[A/G]GGCCTCCGGTGCGGC | 84749 |
| rs747473672 | snp | C/T | 1.6557e-05 | 0.00287719 | missense, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088265 | GTGGAGCCAGAACCT[C/T]CTTTCTCACGGGAAG | 84749 |
| rs747485224 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109029888 | TGATTAACATTAATG[G/T]TACCCTATCTGTTAA | 84749 |
| rs747489498 | in-del | -/CACACACA | | | intron-variant | USP30 | GRCh38.p7 | 12:109081624 | ACGCACGCATGCGCG[-/CACACACA]CACACACACACACAC | 84749 |
| rs747494434 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109031852 | CTCGGGCTTGTAATC[C/G]TAGCACTTTGGGAGG | 84749 |
| rs747502403 | in-del | -/GCTG | | | intron-variant | USP30 | GRCh38.p7 | 12:109075859 | TTTTTTTTTTTTTTT[-/GCTG]TTGGTCCATATGAGT | 84749 |
| rs747510118 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109031351 | CCACTTTTTTACTCA[C/T]TTAACTCAGTTTTTT | 84749 |
| rs747584464 | snp | C/T | 3.31625e-05 | 0.00407188 | intron-variant | USP30 | GRCh38.p7 | 12:109085633 | GTCTTTTTGTTAAAA[C/T]TGTAAACCCCTGACA | 84749 |
| rs747595765 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109062800 | TTGTGCAGCAGTCAC[A/G]GCCATCCCTCTCTAG | 84749 |
| rs747647737 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109083391 | GTGAATTTCTTTTTT[C/T]GGTCATGTCATTTCC | 84749 |
| rs747669700 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109032634 | GAGTAGATCAGTGGT[G/T]GCTTAGGAATGGGGT | 84749 |
| rs747684889 | snp | A/T | 1.74178e-05 | 0.00295103 | intron-variant | USP30 | GRCh38.p7 | 12:109073415 | GCTAAAAGTGACATA[A/T]CAAAAAACTTTTTGC | 84749 |
| rs747684929 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109062659 | AGTGTATTGGTCTTA[C/T]AGTTTGTCTTCTGTG | 84749 |
| rs747712472 | snp | G/T | 1.70679e-05 | 0.00292124 | intron-variant | USP30 | GRCh38.p7 | 12:109073564 | CACTTGATATTTCCG[G/T]GAGAGGTTTTCCAAA | 84749 |
| rs747733724 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055224 | TGAAGTTAGGAAATC[C/T]TTAATTTTATAAATA | 84749 |
| rs747734752 | in-del | -/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109065229 | CTTCTGTATTTTTTT[-/C]CTCTCACACTCTAGC | 84749 |
| rs747803669 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055678 | CTGGGATTACAGGCA[C/T]GAGCCATCACACCTG | 84749 |
| rs747880124 | snp | C/T | 1.65157e-05 | 0.0028736 | intron-variant | USP30 | GRCh38.p7 | 12:109067482 | TCTGGTTAGTTGTTA[C/T]GCTGATGAATTTAAT | 84749 |
| rs747957066 | snp | C/T | 1.65858e-05 | 0.00287969 | missense | USP30 | GRCh38.p7 | 12:109082679 | TTGAAGCCAAGGGAA[C/T]GTTGAACGGGGAAAA | 84749 |
| rs748015329 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109078963 | AGTGTCATTTATATC[A/G]TTCTTGTCTATGTAA | 84749 |
| rs748021617 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109028113 | GCATTTCCCTAATAA[C/T]TAACAATGTTGAGCA | 84749 |
| rs748162299 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109044215 | TAGGAACTGAGGAGC[A/G]TGTAGAATGAGGAGT | 84749 |
| rs748199666 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109049410 | GAACATACACAATAC[C/T]GATTAAGTTGGCTGG | 84749 |
| rs748204443 | in-del | -/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109083461 | AAGATCACTGAGCCT[-/C]TTCTGGGGGTTGAAA | 84749 |
| rs748225616 | snp | C/G | 1.64914e-05 | 0.00287149 | missense | USP30 | GRCh38.p7 | 12:109071673 | AGCGAGACCGCCAGC[C/G]TCGGGTCACACATTT | 84749 |
| rs748242163 | snp | A/G | 1.65765e-05 | 0.00287888 | intron-variant | USP30 | GRCh38.p7 | 12:109071607 | AATGCTTTGCCCTAT[A/G]ACAGGATGCTCACGA | 84749 |
| rs748339032 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | USP30 | GRCh38.p7 | 12:109085752 | GTCACTTACCGACGG[C/T]CCCCACCTTCTGCCA | 84749 |
| rs748345932 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109071404 | ACCTGGCTTTCTCTC[C/T]TGCTCTCTGCTCCTG | 84749 |
| rs748384220 | snp | C/T | | | missense | USP30 | GRCh38.p7 | 12:109085016 | CCTGCTCCCCATCTT[C/T]ATTGCCAACGCTGTC | 84749 |
| rs748390544 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109035787 | ATTACATCTTTAGGC[A/T]TTGTGTGCCCATCAG | 84749 |
| rs748443958 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109050863 | TACAAAAAAATTAGC[A/C]GGGCGTGGTGGTGTG | 84749 |
| rs748484336 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109024624 | AACTGGTAAAGCAGC[A/G]TTTTTTTTTTCCCGA | 84749 |
| rs748516349 | snp | C/T | 1.65334e-05 | 0.00287514 | synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088272 | CAGAACCTTCTTTCT[C/T]ACGGGAAGACTGTGG | 84749 |
| rs748535122 | snp | C/T | 4.97979e-05 | 0.00498964 | intron-variant | USP30 | GRCh38.p7 | 12:109056673 | CAGTAAACTTGTTTT[C/T]TTTTTTAGATATAAA | 84749 |
| rs748624647 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109058887 | ATTTGCAGCCCTGTC[C/T]AGCTGTTGGACAATA | 84749 |
| rs748687122 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109060007 | CCATACTACCCTGAA[C/T]TTACCTGATCTCATC | 84749 |
| rs748757218 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109031202 | ATTAATGTGACTACA[C/T]GCATTGGAAATGGCA | 84749 |
| rs748798078 | snp | G/T | 1.72946e-05 | 0.00294058 | intron-variant | USP30 | GRCh38.p7 | 12:109073573 | TTTCCGGGAGAGGTT[G/T]TCCAAAAGTTAGGAT | 84749 |
| rs748812232 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109045900 | TAGACATAGCTATAC[A/T]TGTAGACATAGATAT | 84749 |
| rs748813898 | snp | A/G | 3.30442e-05 | 0.0040646 | missense, intron-variant | USP30 | GRCh38.p7 | 12:109056692 | TTTAGATATAAAGTC[A/G]TGAAGAACTGGGGAG | 84749 |
| rs748886887 | snp | A/G | 1.64827e-05 | 0.00287073 | missense, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088336 | AGTAAGCTCCCGTGG[A/G]CCAGCGGCAGCCTGA | 84749 |
| rs748904721 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109081824 | GACTATAAAACTTTA[G/T]TGCCTGCATACATCA | 84749 |
| rs749009377 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109067005 | CATGAAAAATTACAT[A/T]CATTCAGTAAACATA | 84749 |
| rs749035027 | snp | A/G/T | 0.000348882 | 0.0132034 | synonymous-codon, missense, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088250 | AAGTCAGATTCACCC[A/G/T]TGGAGCCAGAACCTT | 84749 |
| rs749074724 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109071259 | ATCATTCATGTTAAG[A/G]TGATAAATGTTATGA | 84749 |
| rs749106668 | snp | A/G | 1.6483e-05 | 0.00287076 | intron-variant | USP30 | GRCh38.p7 | 12:109067639 | ACAGGTGAGTACAAC[A/G]TTTGAACAGGTTTAG | 84749 |
| rs749116434 | in-del | -/AT | | | intron-variant | USP30 | GRCh38.p7 | 12:109044743 | CAAATGCTGTAATAA[-/AT]ATGTTTATTCTTCTA | 84749 |
| rs749122506 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109075735 | ATTTCCCTGATGATT[A/G]GTGATATTGAGTGCC | 84749 |
| rs749170259 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109040843 | GGCTTTGGAATTCAC[A/G]TAGCATCACTCTCAC | 84749 |
| rs749173778 | in-del | -/ATTTT | | | intron-variant | USP30 | GRCh38.p7 | 12:109073919 | CTGTCACCCCAATCC[-/ATTTT]ATTTTATTTTATTTT | 84749 |
| rs749212022 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109025919 | TCTCAAACTCCTGGG[C/T]TCAAGGGATCCTCCC | 84749 |
| rs749290772 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109039814 | TGTGGTTTCACCATG[C/T]TGGCCAGGATGATCT | 84749 |
| rs749334037 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109026986 | TCAGCCCCACCTGCA[G/T]GACCTTCTGTAACCC | 84749 |
| rs749340167 | snp | C/T | 1.65081e-05 | 0.00287293 | intron-variant | USP30 | GRCh38.p7 | 12:109072290 | CAGTCTGTTTTTTTT[C/T]TTTCTCCCCTACAGC | 84749 |
| rs749343833 | snp | A/C/G | 3.32382e-05 | 0.00407654 | missense | USP30 | GRCh38.p7 | 12:109085875 | TACCTGCTGTTCTAC[A/C/G]AGCGCGTCCTTTCCA | 84749 |
| rs749361404 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109062983 | ATGTACCTCATTAAG[C/T]GGACTCATATAATAT | 84749 |
| rs749364866 | snp | C/T | 1.8177e-05 | 0.00301466 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052643 | CGGCGGCGGCGGTAG[C/T]GGAGGAGACGGTTTC | 84749 |
| rs749418379 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109077605 | TTAACTAGCTTGACA[A/G]TCTTTTAGTTGGAAT | 84749 |
| rs749468513 | snp | A/G | 3.29462e-05 | 0.00405857 | missense | USP30 | GRCh38.p7 | 12:109081996 | GAATCAGTGCGGGAT[A/G]TTGTGTGTGACAACT | 84749 |
| rs749490112 | snp | A/G | 2.11111e-05 | 0.00324886 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109085959 | GCAAGGCTAGAGCTG[A/G]TGGCACTGTCTGCAC | 84749 |
| rs749573660 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109063958 | GCTCACTGCGACCTC[C/T]GCCTCCTGAGTTCTA | 84749 |
| rs749573994 | snp | A/C | | | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022012 | ATCACAGGCTCATCC[A/C]AGCATACCCAGCTAA | 84749 |
| rs749628277 | snp | A/G | 1.65239e-05 | 0.00287431 | missense | USP30 | GRCh38.p7 | 12:109071619 | TATGACAGGATGCTC[A/G]CGAATTATTCCATGT | 84749 |
| rs749631083 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109035456 | GCAACCTCCGCCTCC[C/T]GGGTTCAAGCGATTC | 84749 |
| rs749635745 | snp | C/T | 1.69295e-05 | 0.00290937 | missense | USP30 | GRCh38.p7 | 12:109083044 | GAGCTGCAGGATGGG[C/T]CGGGAGCCCCCACAC | 84749 |
| rs749728593 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109072171 | GGCTACCTTTAGAAA[C/T]CTGAGCTTTGTTAAA | 84749 |
| rs749730538 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109057546 | GAACAATTGTTTTCT[C/T]CTGTTCTGAGAAACA | 84749 |
| rs749733014 | snp | C/T | 1.64808e-05 | 0.00287057 | missense, synonymous-codon, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088406 | CCTTATGCCGGAAGA[C/T]AAAGTCTCTGCAGGC | 84749 |
| rs749760649 | snp | G/T | 3.29924e-05 | 0.00406142 | missense | USP30 | GRCh38.p7 | 12:109071678 | GACCGCCAGCCTCGG[G/T]TCACACATTTGTTTG | 84749 |
| rs749839720 | snp | A/C/G | 3.48705e-05 | 0.00417541 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052797 | GCTGCCGAAGAGGCC[A/C/G]GGACCAGGGTCCCCA | 84749 |
| rs749894703 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109025098 | CTCTTTCTCCAGGAG[A/C]TGTTTCTTCTCCTGC | 84749 |
| rs749898388 | snp | C/G | 1.90015e-05 | 0.00308227 | intron-variant | USP30 | GRCh38.p7 | 12:109082634 | CCTATTTTAGGCATT[C/G]CTGCAGAGAAATGTT | 84749 |
| rs749904458 | snp | G/T | 1.87855e-05 | 0.0030647 | stop-gained | USP30 | GRCh38.p7 | 12:109085926 | GAGTGCAAGTCTGAA[G/T]AATGACTGTGCCCTC | 84749 |
| rs749955281 | snp | C/T | 9.90671e-05 | 0.00703731 | synonymous-codon | USP30 | GRCh38.p7 | 12:109085862 | GTCCTCCAGCGCCTA[C/T]CTGCTGTTCTACGAG | 84749 |
| rs749960868 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109073313 | AGGAAAGCTATTTCA[A/G]TGTACTTTTCAAGAA | 84749 |
| rs749963128 | snp | A/G | | | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109086007 | AAACTGTACTGTTGC[A/G]TGTGCAAGCGGCCCC | 84749 |
| rs749989908 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046226 | CCTGCCTCAGCCTCC[C/G]TAGTACCTGGGACTA | 84749 |
| rs750019401 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109024554 | TGAGCCACCGTGCCC[A/G]GCCACAATGATTAAT | 84749 |
| rs750065979 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109061636 | GCTGGTCTCGAACTC[C/G]TAAGCTCAAGCAATC | 84749 |
| rs750080971 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109045801 | GTTCTCCAGAGAAAC[A/G]GAATCAATAGAACGC | 84749 |
| rs750116731 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109059899 | GGTATTATACAGAGT[A/G]CAATGTATGCACAAA | 84749 |
| rs750125227 | snp | A/C | 1.70513e-05 | 0.00291982 | intron-variant | USP30 | GRCh38.p7 | 12:109058128 | CTAGATGGGAATTTC[A/C]AGGGAATTATGTACC | 84749 |
| rs750138791 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109032060 | TGAGCCATGATTGTG[A/C]CACTGCCCTCCAAAC | 84749 |
| rs750142406 | snp | A/G | 6.64838e-05 | 0.0057652 | synonymous-codon | USP30 | GRCh38.p7 | 12:109082740 | ACAGTTAAAACTAGG[A/G]AAGGTGAGCCCACAC | 84749 |
| rs750184160 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109058257 | AGAGCCCAATAGATA[A/C]AAACAAGTATTTTTT | 84749 |
| rs750245843 | snp | A/G | 0.000142339 | 0.00843499 | intron-variant, synonymous-codon | USP30 | GRCh38.p7 | 12:109083073 | ACCAGGTGTGTGCGC[A/G]CGAGGAGCCGATGCA | 84749 |
| rs750328703 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109030978 | CATCTTAAATATATA[C/T]AGTATTTTTAAAATC | 84749 |
| rs750377909 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109067936 | CACCTGGGTTCTTTA[C/G]AAAGAGGCAGGTGAC | 84749 |
| rs750379422 | in-del | -/A | 1.67652e-05 | 0.00289522 | frameshift-variant, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088230 | AGTAAGCAAAATTTT[-/A]CGAAAAGTCAGATTC | 84749 |
| rs750407649 | snp | C/T | | | intron-variant, synonymous-codon | USP30 | GRCh38.p7 | 12:109083169 | AGCACAAGGCTTGTA[C/T]AATGGTGCTTAAACT | 84749 |
| rs750451196 | snp | A/C | 3.08019e-05 | 0.00392429 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052808 | GGCCGGGACCAGGGT[A/C]CCCAGCTTGGGCCCG | 84749 |
| rs750483957 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109070533 | CTTTGTAGGCCAGAT[A/G]AGAATGGTAGGTTTT | 84749 |
| rs750540227 | snp | A/G | 4.99838e-05 | 0.00499894 | intron-variant | USP30 | GRCh38.p7 | 12:109073537 | GTGAACACCAGGTAA[A/G]TACAATACCAACACT | 84749 |
| rs750544906 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109077483 | AGTCTATTTGAATGA[C/T]TCATTTTTAATCTAG | 84749 |
| rs750625217 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109026869 | CCAGCTTGCAGATGG[C/T]CACCTTCTCTCTGTG | 84749 |
| rs750625356 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109041857 | AGGATCCCTCTGTCA[A/G]TTGAAGCACAACCAG | 84749 |
| rs750712233 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109079340 | TTTCTTTTCTTTTTC[-/T]TTTTTTTTTTCTTTT | 84749 |
| rs750795617 | in-del | -/C | 1.65108e-05 | 0.00287317 | frameshift-variant, intron-variant | USP30 | GRCh38.p7 | 12:109072305 | TTTTCTCCCCTACAG[-/C]AGCAGTCAGAAATAA | 84749 |
| rs750801879 | in-del | -/AAAG | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | USP30, USP30-AS1 | GRCh38.p7 | 12:109054559 | ATAAAAATAAGAAAA[-/AAAG]AAAGAATAGCTTTCA | 84749 |
| rs750822871 | snp | A/C | 1.64738e-05 | 0.00286995 | missense, utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109067545 | CCTGCCAAGAAGTTA[A/C]TGATGATGAGGTCTT | 84749 |
| rs750840635 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109067333 | CATGTTAGCCAGGAT[C/G]ATCTGGATCTCCTGA | 84749 |
| rs750855825 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109027858 | CTGCTATAAACATTG[A/G]TCTACAGTGTATCCC | 84749 |
| rs750934552 | snp | A/T | 1.6671e-05 | 0.00288708 | intron-variant | USP30 | GRCh38.p7 | 12:109072384 | AATATAACACATAAG[A/T]TGTGGACTTTTAAGA | 84749 |
| rs750981556 | snp | A/G | | | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022817 | AACCAATTATACAGT[A/G]GTACTCAAGCTCCAA | 84749 |
| rs751009413 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109065011 | CAGAAGCCTGGACTT[C/T]ATTATTATTTTTTTA | 84749 |
| rs751015493 | snp | A/G | 3.32646e-05 | 0.00407814 | missense | USP30 | GRCh38.p7 | 12:109085066 | CTCCCAGTTGTTCCC[A/G]ACTACAGGTGAGCCA | 84749 |
| rs751025816 | snp | A/G | 1.64738e-05 | 0.00286995 | missense, utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109067562 | GATGATGAGGTCTTA[A/G]ATGCAAGCTGCTTGT | 84749 |
| rs751034547 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109036521 | CTGGCAGGTCTCAAA[C/T]TCCAGACCTGAGGTG | 84749 |
| rs751039409 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109035308 | GTTATTTTCTTAGTA[G/T]TTGCCCTGGAGATTA | 84749 |
| rs751109935 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109085613 | CTTTTGTTTTTGCCT[A/G]TAAAGTCTTTTTGTT | 84749 |
| rs751123319 | snp | A/G | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | USP30, USP30-AS1 | GRCh38.p7 | 12:109051772 | ATGGGGTTTCACCAT[A/G]TTGGCCAAGCTGGTC | 84749 |
| rs751207945 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109073107 | TTATCTCGCTTTATG[C/G]AATGTTCACTTGTGG | 84749 |
| rs751218633 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109058666 | GAAATCCACTGCCAC[A/G]TAAACAGTTTCATCG | 84749 |
| rs751234677 | snp | C/T | | | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109087178 | GGAATTTTGATGACA[C/T]AGTAGTACCTATGTT | 84749 |
| rs751274535 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109045591 | GGCCAAGTCAATTCA[A/C]TTCTCCGGGCTTTAG | 84749 |
| rs751298148 | snp | C/T | 5.3968e-05 | 0.00519433 | intron-variant, synonymous-codon, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052682 | GGTGCGGCTGCAATG[C/T]TGAGCTCCCGGGCCG | 84749 |
| rs751327276 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109059575 | CTGGAGTGCAGTAGC[A/G]CGATCTCAGCTCACT | 84749 |
| rs751331290 | snp | A/G | 0.000128725 | 0.00802159 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052638 | GGCGGCGGCGGCGGC[A/G]GTAGCGGAGGAGACG | 84749 |
| rs751375519 | snp | C/T | 1.65416e-05 | 0.00287586 | missense | USP30 | GRCh38.p7 | 12:109072345 | AAATTACCTGCCGCA[C/T]AAGAGGTAGCTGTTT | 84749 |
| rs751391380 | snp | C/T | 3.99568e-05 | 0.00446954 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109085942 | AATGACTGTGCCCTC[C/T]TGCAAGGCTAGAGCT | 84749 |
| rs751485055 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109057650 | TAAGTGTTTTTGTAC[A/G]TTTAGGAAGAACCAA | 84749 |
| rs751496988 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109071958 | ATAAAGAATGTGTTA[-/T]TTTTTTCCTGTTTAA | 84749 |
| rs751507270 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109080415 | GTAGCTCTCCGTTCA[C/T]TCAAACGGTTTTGTT | 84749 |
| rs751559851 | snp | C/T | 3.48159e-05 | 0.00417214 | intron-variant | USP30 | GRCh38.p7 | 12:109082648 | TGCTGCAGAGAAATG[C/T]TCCTTTTATTTCAGA | 84749 |
| rs751579792 | snp | A/G | | | utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109024862 | CTGATCTCGTGATCC[A/G]CCTGCCTTGGCCCCC | 84749 |
| rs751649936 | snp | A/G | 1.64844e-05 | 0.00287087 | missense, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088318 | GTCGGGTGGTTCATC[A/G]TTAGTAAGCTCCCGT | 84749 |
| rs751655389 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109067160 | ACTCTGTCACCCAGG[C/G]TGGAGTGCAGTGGCA | 84749 |
| rs751680975 | snp | C/G | 1.65548e-05 | 0.002877 | intron-variant | USP30 | GRCh38.p7 | 12:109067673 | GGAGAATCCTTTCCC[C/G]TAGTGACTTGGGGCC | 84749 |
| rs751722909 | snp | C/G | 1.65575e-05 | 0.00287724 | missense, intron-variant | USP30 | GRCh38.p7 | 12:109056781 | TACAGAAAGAAAGAA[C/G]CGTAGAAAAGGTAAG | 84749 |
| rs751762514 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109039532 | TATAAGGAGATGATA[C/T]AGAAGCCAGCATTTA | 84749 |
| rs751819380 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053122 | AATCCTTCTAGTATA[A/C]CCCCAGTCCTTCTGG | 84749 |
| rs751821758 | snp | A/G | 1.65053e-05 | 0.0028727 | synonymous-codon | USP30 | GRCh38.p7 | 12:109082974 | GTACCACCTCCTTGG[A/G]CATAAACCTAGTCAA | 84749 |
| rs751853216 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon | USP30 | GRCh38.p7 | 12:109085691 | ATACCTCTTCCGGCT[A/G]ATGGCAGTTGTCGTC | 84749 |
| rs751853440 | in-del | -/GCACTGTCT | 4.28568e-05 | 0.00462889 | cds-indel | USP30 | GRCh38.p7 | 12:109085962 | AGGCTAGAGCTGATG[-/GCACTGTCT]GCACTGTCCAGGAAA | 84749 |
| rs751899558 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109026690 | CCAGGCTGGTCTCAA[A/C]CTCCTGCATTCAAGC | 84749 |
| rs751954827 | snp | A/T | 1.68556e-05 | 0.00290302 | intron-variant | USP30 | GRCh38.p7 | 12:109085107 | GCCCCATCTTAGAGC[A/T]ACCACTGCTCTTAGC | 84749 |
| rs751970007 | snp | A/T | 1.68159e-05 | 0.0028996 | intron-variant | USP30 | GRCh38.p7 | 12:109073550 | AAATACAATACCAAC[A/T]CTTGATATTTCCGGG | 84749 |
| rs751982732 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109027620 | TGCCTACTCTAGTTA[C/T]CTGATAAGAGTGGAA | 84749 |
| rs752159382 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109033805 | CTTGGTTAAGAGGTT[A/G]AGCCCTTGTTAAATA | 84749 |
| rs752164179 | snp | A/G | 0.000185856 | 0.00963813 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054025 | AACCTGCATCTGTGG[A/G]GTTGTTTTAAAAATG | 84749 |
| rs752201299 | in-del | -/TTTGTG | 1.67293e-05 | 0.00289212 | intron-variant | USP30 | GRCh38.p7 | 12:109056636 | TCTGTATATTTGCCT[-/TTTGTG]TTTGTGTGAGGGAAG | 84749 |
| rs752207996 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109049828 | TGCAAAAAAGAAAAG[A/G]AAAAAAAAAGTTTGA | 84749 |
| rs752225012 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054073 | GGCCTGGCAGAGAGT[A/G]TGTACCCTTAAATAT | 84749 |
| rs752268227 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109064923 | ATGGGAGAAAGATGT[C/G]GTTCATTTCCCAACC | 84749 |
| rs752289385 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109085287 | AATTTACATATGCAT[A/T]TGTATGTGTGTATAT | 84749 |
| rs752292174 | in-del | -/A | | | intron-variant | USP30 | GRCh38.p7 | 12:109074502 | CACCGGCAGTGTATG[-/A]GGGGTTCCAATTTCT | 84749 |
| rs752348838 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon | USP30 | GRCh38.p7 | 12:109085703 | GCTGATGGCAGTTGT[C/T]GTCCACCATGGAGAC | 84749 |
| rs752395880 | in-del | -/A | 1.66485e-05 | 0.00288513 | intron-variant | USP30 | GRCh38.p7 | 12:109081320 | TTCTGGATTTTCTGC[-/A]ATATTTCTTTCAGAG | 84749 |
| rs752559763 | snp | A/G | | | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022540 | CTTTGCAACAATCCT[A/G]TGAGCAGGTGTGATT | 84749 |
| rs752667007 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109043757 | TTTAAAACTTTTGCG[C/T]ATCAAAAGACACTAT | 84749 |
| rs752720022 | snp | C/T | 4.97286e-05 | 0.00498616 | synonymous-codon | USP30 | GRCh38.p7 | 12:109082863 | TCAGTGTCTCTGCAT[C/T]CACCTACAGCGGCTG | 84749 |
| rs752774363 | snp | A/G | 5.37707e-05 | 0.00518483 | intron-variant, synonymous-codon | USP30 | GRCh38.p7 | 12:109083076 | AGGTGTGTGCGCGCG[A/G]GGAGCCGATGCAGCA | 84749 |
| rs752774593 | snp | C/T | 1.66613e-05 | 0.00288623 | missense | USP30 | GRCh38.p7 | 12:109083021 | ACAAGAACCCAGGGC[C/T]TACACTGGAGCTGCA | 84749 |
| rs752790580 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109061391 | TGTCTCTAACTTTGG[C/T]TTAAAAAAAAAAAAA | 84749 |
| rs752801173 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109080327 | AGGAAAAAAAGCCAC[A/G]AACACACAAATCTCG | 84749 |
| rs752804123 | in-del | -/TC | | | intron-variant | USP30 | GRCh38.p7 | 12:109063594 | GGATCAAATGGTAAT[-/TC]TGTTTAATTTTTTGA | 84749 |
| rs752824291 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109045285 | CGCCCGCCCAAACAT[A/C]TTTCCAAAGGGATAA | 84749 |
| rs752839302 | snp | C/T | 1.68202e-05 | 0.00289996 | missense, synonymous-codon, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088487 | CATCTCGGTGCTCCC[C/T]GATGTGGTCACAGCC | 84749 |
| rs752857158 | snp | C/T | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | USP30, USP30-AS1 | GRCh38.p7 | 12:109052024 | GCGTCAAAAAACTTA[C/T]TATTTCTTCAAATTT | 84749 |
| rs752894102 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109033895 | ATACAAGATGTCTAA[C/T]CAGTACAATAACTAG | 84749 |
| rs752962678 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109066510 | CAACATGGGGGAACC[C/T]CCATCTCTACTAAAA | 84749 |
| rs752996506 | snp | C/T | 1.64806e-05 | 0.00287054 | intron-variant | USP30 | GRCh38.p7 | 12:109081921 | AGTAATTTTCTTCTT[C/T]TCATGCTGTAGGGTC | 84749 |
| rs753067108 | snp | A/G | 3.29533e-05 | 0.00405901 | missense | USP30 | GRCh38.p7 | 12:109085822 | CCGATGACACTGTCC[A/G]CAAGGCCAGCCTGCA | 84749 |
| rs753115418 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053020 | ATTGTTCCCAGGACA[A/C]CCGGGGCACTCCAGT | 84749 |
| rs753115591 | snp | C/G | 3.29527e-05 | 0.00405898 | missense | USP30 | GRCh38.p7 | 12:109081382 | TCACTAAGTATTCCA[C/G]CCGCCACATGGGTAT | 84749 |
| rs753143746 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109075080 | AATATTCCATTATAT[A/G]TGTATACCACATTTT | 84749 |
| rs753190348 | snp | A/G | 3.30644e-05 | 0.00406585 | missense, intron-variant | USP30 | GRCh38.p7 | 12:109057937 | TTAGGGCTTGTGCCT[A/G]GCCTTGTTAATTTAG | 84749 |
| rs753253713 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109048560 | GCCTGGCCAACATGG[C/T]GAAACCCCATCTCTA | 84749 |
| rs753299624 | snp | A/T | | | missense | USP30 | GRCh38.p7 | 12:109073484 | GTCTCAACATCCTTT[A/T]CATGGAAGACTCACT | 84749 |
| rs753304919 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109061744 | ATACAAGTAATGCAT[G/T]AATCAGTTCTCTTTG | 84749 |
| rs753307854 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109047200 | CGAGGAAACCCTTCT[G/T]ATGTTCATTCAACAT | 84749 |
| rs753309417 | in-del | -/TG | | | intron-variant | USP30 | GRCh38.p7 | 12:109074707 | TTTGATGTATGACTG[-/TG]TGTGTGTGTGTGTGC | 84749 |
| rs753339207 | in-del | -/CAC | 1.64732e-05 | 0.0028699 | cds-indel | USP30 | GRCh38.p7 | 12:109081963 | CTGGACCACTGCCTT[-/CAC]CACTTCATCTCATCA | 84749 |
| rs753341509 | snp | A/G | 1.64779e-05 | 0.00287031 | missense | USP30 | GRCh38.p7 | 12:109085831 | CTGTCCGCAAGGCCA[A/G]CCTGCAGGAGGTCCT | 84749 |
| rs753361557 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | USP30 | GRCh38.p7 | 12:109085717 | TCGTCCACCATGGAG[A/G]CATGCACTCTGGACA | 84749 |
| rs753474257 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109048312 | CTCGTCTCAGACTCC[C/T]GGGTTCAAGGGGTCC | 84749 |
| rs753475948 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109032504 | TGTAATATGGAAGAA[C/T]CTTAAGAACATTGTG | 84749 |
| rs753527526 | snp | C/T | 3.29468e-05 | 0.00405861 | synonymous-codon | USP30 | GRCh38.p7 | 12:109081953 | CCCATTGACCCTGGA[C/T]CACTGCCTTCACCAC | 84749 |
| rs753589445 | snp | A/G | 1.65425e-05 | 0.00287593 | missense | USP30 | GRCh38.p7 | 12:109082874 | GCATCCACCTACAGC[A/G]GCTGAGCTGGTCCAG | 84749 |
| rs753620524 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109084490 | ACATTTTTGGTTATC[A/T]CTACTGGGGGAGGGG | 84749 |
| rs753634176 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109033218 | TTAAAACATGTTATT[C/T]GAGAAGGAAGAATTA | 84749 |
| rs753663319 | snp | A/C | 1.64898e-05 | 0.00287135 | missense | USP30 | GRCh38.p7 | 12:109082938 | GCAGTTCAATGAGTT[A/C]CTGATGATGGACATT | 84749 |
| rs753683125 | snp | A/C | 1.67298e-05 | 0.00289217 | intron-variant | USP30 | GRCh38.p7 | 12:109071581 | TCTTGCCTCTTCCAA[A/C]CTCTCTAAAGAATGC | 84749 |
| rs753711580 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109069156 | TTTAAGACAGTCTAG[C/T]GCTACAGTGCACATT | 84749 |
| rs753820007 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109043651 | TAGGGCAAAACCTTT[A/G]TGACATTGGATTTGG | 84749 |
| rs753851353 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109078410 | GTCTGGGCGACAGAG[A/T]GAGACTGAGTCTCAA | 84749 |
| rs753871566 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109070778 | GGATCCAGCAACCCC[A/G]CTGCTGGGTACAAAC | 84749 |
| rs753877805 | snp | C/T | 0.000131865 | 0.00811882 | synonymous-codon | USP30 | GRCh38.p7 | 12:109071648 | GTCATTACCTCGTCA[C/T]TGGAAGATGAGCGAG | 84749 |
| rs753946613 | snp | A/G | 1.66078e-05 | 0.00288161 | intron-variant | USP30 | GRCh38.p7 | 12:109072364 | AGGTAGCTGTTTTCC[A/G]TTGAAATATAACACA | 84749 |
| rs753957236 | snp | C/T | 1.691e-05 | 0.0029077 | intron-variant | USP30 | GRCh38.p7 | 12:109084944 | GACTCGGGCCTTTTT[C/T]TCTTGCAGTTCTGAA | 84749 |
| rs753958960 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109042318 | AAAATTCACTAAGAA[C/T]AAAAAGATGTTCCTT | 84749 |
| rs754055986 | snp | C/T | 1.65553e-05 | 0.00287705 | synonymous-codon | USP30 | GRCh38.p7 | 12:109073523 | GGTCTGCAAACACTG[C/T]GAACACCAGGTAAAT | 84749 |
| rs754057438 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109080266 | TGTCGTCTGACCACT[C/T]AATCCTGTAGGATGC | 84749 |
| rs754084973 | snp | C/T | 1.65649e-05 | 0.00287788 | missense, intron-variant | USP30 | GRCh38.p7 | 12:109058082 | CACACCAGTATTTAT[C/T]CTTAACACTCTTGCA | 84749 |
| rs754106501 | snp | C/T | 0.000117085 | 0.0076504 | intron-variant, missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052701 | GCTCCCGGGCCGAGG[C/T]GGCGATGACCGCGGC | 84749 |
| rs754192486 | snp | C/G | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | USP30, USP30-AS1 | GRCh38.p7 | 12:109051812 | TGACCTCAGGTGATC[C/G]ACCAGCCTCGTTCTC | 84749 |
| rs754213446 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109041980 | AATTATAAAAAAATT[A/G]TAGAAACTCAAATAA | 84749 |
| rs754224659 | snp | G/T | 1.96926e-05 | 0.00313782 | intron-variant | USP30 | GRCh38.p7 | 12:109082629 | GCTGTCCTATTTTAG[G/T]CATTGCTGCAGAGAA | 84749 |
| rs754293527 | snp | A/G | | | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109087324 | CTTCCTCTGCTGGGG[A/G]TGAGCTGGCAGACAC | 84749 |
| rs754374279 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109045546 | ACCCGCCTGCCATAC[C/T]GTCTGGTCACAAACC | 84749 |
| rs754377417 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109036935 | CTCTTGGAGTTCATT[A/G]AGCTTCTTTGATGTA | 84749 |
| rs754382464 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109085660 | GACATGTGTTCGTAT[C/T]ATTCAGCTCCTCCAC | 84749 |
| rs754546738 | snp | A/C | | | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109021386 | GCCAGGCACTGTAAT[A/C]GGCACTGGGGGTATG | 84749 |
| rs754564771 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109033525 | CCTTGGAGCAATGCT[A/G]TGTGCCCTGAGTACT | 84749 |
| rs754572292 | snp | C/G | 1.64735e-05 | 0.00286993 | missense, utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109067572 | TCTTAGATGCAAGCT[C/G]CTTGTTGGATGTCTT | 84749 |
| rs754641363 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109069324 | TGAGGGCTCCTTGAG[C/T]CTCCCAGGAAGTGCT | 84749 |
| rs754642565 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109083318 | AAACGCTTAAAATTG[C/T]AGCTTTGCCTTCTAA | 84749 |
| rs754688647 | snp | C/T | 1.6522e-05 | 0.00287414 | missense | USP30 | GRCh38.p7 | 12:109085022 | CCCCATCTTTATTGC[C/T]AACGCTGTCAGCGCC | 84749 |
| rs754691473 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109048376 | TAGGTGTGAGCCATC[A/G]CGCCTGGCCTGCTTC | 84749 |
| rs754748366 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109067107 | TCCTACAGTCCTTAA[-/T]TTTTTTTTTTTTTTT | 84749 |
| rs754816326 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109042347 | TTTCTGTCCTCAGTC[A/G]TACGGTTCTTTTCCC | 84749 |
| rs754857725 | snp | C/T | 6.08587e-05 | 0.00551595 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109085945 | GACTGTGCCCTCCTG[C/T]AAGGCTAGAGCTGAT | 84749 |
| rs754892664 | snp | C/T | 1.67008e-05 | 0.00288965 | intron-variant | USP30 | GRCh38.p7 | 12:109082760 | TGAGCCCACACTACA[C/T]ACCCTGTTGGCTTTG | 84749 |
| rs754970122 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109061038 | GATCCTCCCATCTTG[A/G]TCTCCCAAAGTGCTG | 84749 |
| rs754981222 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109028056 | TTCTCCTCAACACTT[A/G]TTGATAATAGCCATC | 84749 |
| rs755000159 | snp | C/T | 1.66247e-05 | 0.00288307 | missense, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088249 | AAAGTCAGATTCACC[C/T]GTGGAGCCAGAACCT | 84749 |
| rs755030621 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109048717 | TGCACTCCAGCCTGG[A/G]CAACAGAGTGAGACT | 84749 |
| rs755034884 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109057072 | GTGTTCTCATTAGTA[C/T]GGCAATTGTAGTTTT | 84749 |
| rs755053445 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109043656 | CAAAACCTTTGTGAC[A/G]TTGGATTTGGCAGTG | 84749 |
| rs755086747 | snp | A/G | 4.94385e-05 | 0.0049716 | missense, synonymous-codon, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088385 | AGGGGCTTTTCCCAC[A/G]GGAATCCTTATGCCG | 84749 |
| rs755092887 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109077630 | TGGAATGCTTAGTCC[A/G]TTTACATTTAATGTA | 84749 |
| rs755094945 | in-del | -/AAAAAAG | | | intron-variant | USP30 | GRCh38.p7 | 12:109041640 | ACTCCATTTCAAAAA[-/AAAAAAG]AAAAAAGAAAAAGAA | 84749 |
| rs755109701 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109066192 | AGGAGGTCAAGGCTG[C/T]AGTGAGCCAAGATCA | 84749 |
| rs755227796 | snp | C/T | 1.65348e-05 | 0.00287526 | synonymous-codon | USP30 | GRCh38.p7 | 12:109082995 | ACCTAGTCAACACAA[C/T]CCTAAACTGAACAAG | 84749 |
| rs755230207 | snp | C/T | | | synonymous-codon | USP30 | GRCh38.p7 | 12:109085863 | TCCTCCAGCGCCTAC[C/T]TGCTGTTCTACGAGC | 84749 |
| rs755233873 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109031297 | TCATTCAAACTCTAC[A/T]CATGTGTCCTCAATG | 84749 |
| rs755237483 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109065398 | TTTAGGTACTGCCTA[C/T]GTCAGCCTCAAATAA | 84749 |
| rs755269140 | snp | A/G | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | USP30, USP30-AS1 | GRCh38.p7 | 12:109051850 | GCTGGGATTACAGGC[A/G]TGAGCCACGGCGTCT | 84749 |
| rs755365705 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109035474 | GTTCAAGCGATTCTC[C/T]TGCCTCAGCCTCCTG | 84749 |
| rs755366090 | snp | C/T | 1.67534e-05 | 0.0028942 | intron-variant | USP30 | GRCh38.p7 | 12:109056633 | ATATCTGTATATTTG[C/T]CTTTTGTGTTTGTGT | 84749 |
| rs755463064 | snp | C/T | 3.29674e-05 | 0.00405988 | synonymous-codon, missense, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088329 | CATCATTAGTAAGCT[C/T]CCGTGGGCCAGCGGC | 84749 |
| rs755482392 | snp | C/T | 1.65718e-05 | 0.00287848 | missense, intron-variant | USP30 | GRCh38.p7 | 12:109056782 | ACAGAAAGAAAGAAG[C/T]GTAGAAAAGGTAAGA | 84749 |
| rs755565586 | snp | C/T | | | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109087406 | CTCTTCTGCTGGGCC[C/T]AGGCTGCACCCTGAG | 84749 |
| rs755569330 | snp | A/G | 1.64757e-05 | 0.00287012 | missense | USP30 | GRCh38.p7 | 12:109081344 | TTCAGAGTCCTGTTC[A/G]ATTTGATACCTTTGA | 84749 |
| rs755603377 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109059952 | TGGCAAAAGGAAAGA[A/C]TGTAGATATCAAACA | 84749 |
| rs755657320 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046237 | CTCCCTAGTACCTGG[A/G]ACTACAGGCACATGC | 84749 |
| rs755662856 | in-del | -/GCGC | | | intron-variant | USP30 | GRCh38.p7 | 12:109081619 | TACACACGCACGCAT[-/GCGC]GCACACACACACACA | 84749 |
| rs755666037 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109031004 | AAATCAGGGGATGCT[A/G]AGCAAAGGGTATACC | 84749 |
| rs755669805 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109048371 | GATTATAGGTGTGAG[A/C]CATCGCGCCTGGCCT | 84749 |
| rs755673189 | snp | G/T | 1.65756e-05 | 0.00287881 | intron-variant | USP30 | GRCh38.p7 | 12:109085634 | TCTTTTTGTTAAAAT[G/T]GTAAACCCCTGACAT | 84749 |
| rs755677589 | in-del | -/A | 1.65192e-05 | 0.00287391 | frameshift-variant, intron-variant | USP30 | GRCh38.p7 | 12:109056769 | TTGGGGTCCCATTAC[-/A]GAAAGAAAGAAGCGT | 84749 |
| rs755701706 | in-del | -/TTC | 3.29674e-05 | 0.00405988 | intron-variant | USP30 | GRCh38.p7 | 12:109081913 | TGAATTGTAGTAATT[-/TTC]TTCTTCTCATGCTGT | 84749 |
| rs755717308 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109025129 | CCTTGGACATCAGAA[C/T]TGCAGGCTCTTTAGT | 84749 |
| rs755810229 | snp | A/G | 3.41413e-05 | 0.00413153 | intron-variant | USP30 | GRCh38.p7 | 12:109073565 | ACTTGATATTTCCGG[A/G]AGAGGTTTTCCAAAA | 84749 |
| rs755914088 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109083203 | GAGAACAGCAGGATT[C/G]GGGGTGGAAGAGGGA | 84749 |
| rs755956610 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054826 | CCAAGTTTGGTGCAT[A/G]TTCTGTTGACTCTGT | 84749 |
| rs755961009 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109068224 | AATGAAGTTCTAGAG[A/G]TGAAAAAATCTAGCC | 84749 |
| rs756083727 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053245 | CGCGTTTTGTTAGTA[C/T]CGCCCCCTATTCCTG | 84749 |
| rs756127652 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109069061 | GTTGTCCCCATTTTA[C/T]AGATGGAAAAACACT | 84749 |
| rs756130387 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109073736 | CTGCACCAAGGACAA[A/C]AGACCCACTGTGGAT | 84749 |
| rs756150308 | snp | A/G | 1.65581e-05 | 0.00287728 | synonymous-codon | USP30 | GRCh38.p7 | 12:109082869 | TCTCTGCATCCACCT[A/G]CAGCGGCTGAGCTGG | 84749 |
| rs756150369 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109067590 | TGTTGGATGTCTTAA[A/G]AATGTACAGATGGCA | 84749 |
| rs756191999 | snp | C/G | 1.79213e-05 | 0.00299338 | intron-variant, missense | USP30 | GRCh38.p7 | 12:109083078 | GTGTGTGCGCGCGAG[C/G]AGCCGATGCAGCAGG | 84749 |
| rs756213346 | snp | C/T | | | downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088047 | TGTTCTTTTGTAATA[C/T]ACTGATCTGTTACAA | 84749 |
| rs756268152 | snp | C/T | 0.000151069 | 0.00868974 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052640 | CGGCGGCGGCGGCGG[C/T]AGCGGAGGAGACGGT | 84749 |
| rs756358064 | snp | G/T | 1.66385e-05 | 0.00288426 | intron-variant | USP30 | GRCh38.p7 | 12:109072284 | GGTTTTCAGTCTGTT[G/T]TTTTTTTTTCTCCCC | 84749 |
| rs756366798 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109063785 | TAATGATAAGTTATA[C/T]TGAGCATCTTTTCAT | 84749 |
| rs756373445 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109077557 | GTATTTAAAGTGTGA[C/T]TTTGTGGACAGCATA | 84749 |
| rs756375438 | in-del | -/G | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055000 | CATGATCCAAATACT[-/G]GGATAATAATGTATT | 84749 |
| rs756389266 | snp | A/G | 3.32066e-05 | 0.00407458 | missense | USP30 | GRCh38.p7 | 12:109085873 | CCTACCTGCTGTTCT[A/G]CGAGCGCGTCCTTTC | 84749 |
| rs756418321 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109042113 | CTGTTCAAGGACACC[C/T]ACACATAGGTATCTT | 84749 |
| rs756469489 | snp | G/T | 3.30158e-05 | 0.00406286 | synonymous-codon, intron-variant | USP30 | GRCh38.p7 | 12:109057945 | TGTGCCTGGCCTTGT[G/T]AATTTAGGGAACACC | 84749 |
| rs756488757 | snp | C/G | 1.67691e-05 | 0.00289556 | intron-variant | USP30 | GRCh38.p7 | 12:109056813 | ATGAGAACACTGCAT[C/G]ATGGTCTGTAGACTT | 84749 |
| rs756557532 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon | USP30 | GRCh38.p7 | 12:109081941 | GCTGTAGGGTCACCC[A/G]TTGACCCTGGACCAC | 84749 |
| rs756588277 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109035324 | TTGCCCTGGAGATTA[C/T]CATTACCATTTCAAT | 84749 |
| rs756635162 | snp | A/G | 1.66974e-05 | 0.00288936 | synonymous-codon | USP30 | GRCh38.p7 | 12:109083025 | GAACCCAGGGCCTAC[A/G]CTGGAGCTGCAGGAT | 84749 |
| rs756652119 | snp | C/T | 1.64808e-05 | 0.00287057 | missense, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088399 | CGGGAATCCTTATGC[C/T]GGAAGACAAAGTCTC | 84749 |
| rs756698423 | in-del | -/TA | | | intron-variant | USP30 | GRCh38.p7 | 12:109035280 | TGTCTTTTCTTTCAC[-/TA]TATATTTTTGAGTTA | 84749 |
| rs756746064 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109072040 | AACAGTATAAATATC[A/G]GAGGAGTTGACAAAA | 84749 |
| rs756782651 | in-del | -/TGTT | 1.75789e-05 | 0.00296465 | utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088200 | AAAAACTGTTAAAAA[-/TGTT]TGTTTTTATTTTTTA | 84749 |
| rs756791203 | snp | A/G | 4.96709e-05 | 0.00498327 | intron-variant | USP30 | GRCh38.p7 | 12:109085637 | TTTTGTTAAAATTGT[A/G]AACCCCTGACATGTG | 84749 |
| rs756803025 | snp | A/G | 1.64969e-05 | 0.00287196 | missense, intron-variant | USP30 | GRCh38.p7 | 12:109057952 | GGCCTTGTTAATTTA[A/G]GGAACACCTGCTTCA | 84749 |
| rs756808794 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109044217 | GGAACTGAGGAGCGT[A/G]TAGAATGAGGAGTTA | 84749 |
| rs756809351 | snp | A/G | 1.6477e-05 | 0.00287024 | synonymous-codon | USP30 | GRCh38.p7 | 12:109081390 | TATTCCAGCCGCCAC[A/G]TGGGTATGTACTGAT | 84749 |
| rs756820181 | snp | C/T | | | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022853 | TATTTATCTAGTAAA[C/T]ATTAATGAGCAACAA | 84749 |
| rs756832558 | snp | A/C | 1.64795e-05 | 0.00287045 | missense | USP30 | GRCh38.p7 | 12:109085836 | CGCAAGGCCAGCCTG[A/C]AGGAGGTCCTGTCCT | 84749 |
| rs756850537 | in-del | -/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109075859 | TTTTTTTTTTTTTTT[-/G]CTGTTGGTCCATATG | 84749 |
| rs756861673 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109036523 | GGCAGGTCTCAAACT[C/G]CAGACCTGAGGTGAT | 84749 |
| rs756862288 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109058680 | CATAAACAGTTTCAT[C/T]GTAAGAAGTATTCTG | 84749 |
| rs756882950 | in-del | -/AATA | | | intron-variant | USP30 | GRCh38.p7 | 12:109044166 | TACTTAGAGTAGTTG[-/AATA]AATAGAGACAAAATG | 84749 |
| rs756885756 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109059605 | TGCAACCTCCGCCTC[C/G]CGGGTTCAAGCGATT | 84749 |
| rs756923408 | snp | A/G | 1.66477e-05 | 0.00288506 | synonymous-codon | USP30 | GRCh38.p7 | 12:109084969 | TCTGAATCAGCCAGG[A/G]GCCCCCAAAACACAG | 84749 |
| rs756934064 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon | USP30 | GRCh38.p7 | 12:109081959 | GACCCTGGACCACTG[C/T]CTTCACCACTTCATC | 84749 |
| rs756972206 | snp | A/G | 3.29696e-05 | 0.00406001 | missense | USP30 | GRCh38.p7 | 12:109071661 | CATTGGAAGATGAGC[A/G]AGACCGCCAGCCTCG | 84749 |
| rs757009452 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054916 | ATTATTATAAAACAG[G/T]GTCAATATTACCACC | 84749 |
| rs757047302 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109045598 | TCAATTCACTTCTCC[A/G]GGCTTTAGCTTCCTC | 84749 |
| rs757083674 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109029563 | TGTTTTACTAGGGCC[C/T]ATTGTATGAGTGTGA | 84749 |
| rs757103071 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109067703 | CTGACCTTAAAATTG[C/T]CTGGCCCCAGTGTAC | 84749 |
| rs757173474 | snp | C/T | 3.29457e-05 | 0.00405854 | missense | USP30 | GRCh38.p7 | 12:109085725 | CATGGAGACATGCAC[C/T]CTGGACACTTTGTCA | 84749 |
| rs757224501 | in-del | -/GTC | 1.64779e-05 | 0.00287031 | intron-variant | USP30 | GRCh38.p7 | 12:109082040 | CATTGAACCCCAAAT[-/GTC]ATCGCCAGCTGGCCT | 84749 |
| rs757294030 | snp | C/T | 3.71588e-05 | 0.00431022 | intron-variant, missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052704 | CCCGGGCCGAGGCGG[C/T]GATGACCGCGGCCGA | 84749 |
| rs757303996 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053151 | GGGTCCCCCAATCAT[A/G]TCAGTTTCTGGACTG | 84749 |
| rs757385205 | snp | A/G | 1.80863e-05 | 0.00300713 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052644 | GGCGGCGGCGGTAGC[A/G]GAGGAGACGGTTTCA | 84749 |
| rs757427307 | snp | C/T | 2.26755e-05 | 0.00336708 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109085963 | GGCTAGAGCTGATGG[C/T]ACTGTCTGCACTGTC | 84749 |
| rs757428980 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109037205 | AATCTGCTGTTGTGC[G/T]CGCTAGTGAATTTTT | 84749 |
| rs757489187 | snp | C/G | 1.6601e-05 | 0.00288101 | missense, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088253 | TCAGATTCACCCGTG[C/G]AGCCAGAACCTTCTT | 84749 |
| rs757539260 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109039559 | TTTAGAACTGATCTA[G/T]TTCCCGAGAAAAAAT | 84749 |
| rs757648403 | snp | C/G | 1.66618e-05 | 0.00288628 | missense | USP30 | GRCh38.p7 | 12:109084967 | GTTCTGAATCAGCCA[C/G]GGGCCCCCAAAACAC | 84749 |
| rs757714356 | snp | C/T | 1.65081e-05 | 0.00287293 | intron-variant | USP30 | GRCh38.p7 | 12:109072292 | GTCTGTTTTTTTTTT[C/T]TCTCCCCTACAGCAG | 84749 |
| rs757730643 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109048551 | TCGAGACCAGCCTGG[C/G]CAACATGGCGAAACC | 84749 |
| rs757839801 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109084610 | CCAAAACCATCATGG[A/T]GCTGCTGTTGAGAAA | 84749 |
| rs757876413 | snp | A/G | 1.71085e-05 | 0.00292471 | intron-variant | USP30 | GRCh38.p7 | 12:109058132 | ATGGGAATTTCAAGG[A/G]AATTATGTACCTTTT | 84749 |
| rs757892111 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109033896 | TACAAGATGTCTAAT[C/T]AGTACAATAACTAGG | 84749 |
| rs757929698 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109083470 | GAGCCTCTTCTGGGG[A/G]TTGAAATGCCTTCTG | 84749 |
| rs757962281 | snp | C/T | 1.64762e-05 | 0.00287016 | stop-gained, intron-variant | USP30 | GRCh38.p7 | 12:109057982 | ATGAACTCCCTGCTA[C/T]AAGGCCTGTCTGCCT | 84749 |
| rs757982948 | snp | C/T | | | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022662 | GACTTAAAACCCCGG[C/T]AGTCTATCTCCACAA | 84749 |
| rs757986438 | snp | A/C | 1.88571e-05 | 0.00307053 | intron-variant | USP30 | GRCh38.p7 | 12:109082635 | CTATTTTAGGCATTG[A/C]TGCAGAGAAATGTTC | 84749 |
| rs757997606 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109024638 | CATTTTTTTTTTCCC[A/G]AGACCGAGTCTCGCT | 84749 |
| rs758007619 | snp | C/T | 7.07656e-05 | 0.00594792 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109085972 | TGATGGCACTGTCTG[C/T]ACTGTCCAGGAAAAA | 84749 |
| rs758025544 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109068204 | TCTGAAGCAGAGGCC[A/G]AGAGAATGAAGTTCT | 84749 |
| rs758027294 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109071909 | TCAAGGCTCTTTCAA[A/G]TGATTCATTGCTGCA | 84749 |
| rs758040855 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109034994 | CCATCCATTTACTTT[G/T]AACCTATTTGTGTCT | 84749 |
| rs758051346 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109038659 | ATGGTTGGATCATTA[C/T]GGTAAGTTTATGTTT | 84749 |
| rs758107424 | snp | C/T | | | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109021753 | TTGTTGAATAAATGG[C/T]TCTCAGTTCAGGCTG | 84749 |
| rs758115333 | in-del | -/ACTAGAGGACTTTG | | | intron-variant | USP30 | GRCh38.p7 | 12:109070087 | TTGCAGCGGGGAGCC[-/ACTAGAGGACTTTG]AACTGGGGACTGGTT | 84749 |
| rs758212493 | in-del | -/C | 1.66382e-05 | 0.00288424 | frameshift-variant, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088247 | GAAAAGTCAGATTCA[-/C]CCGTGGAGCCAGAAC | 84749 |
| rs758244872 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109042603 | TGGATATTTAAATTG[C/T]TTCCAATCCCTTATT | 84749 |
| rs758295013 | snp | C/T | 1.88656e-05 | 0.00307123 | stop-lost | USP30 | GRCh38.p7 | 12:109085929 | TGCAAGTCTGAAGAA[C/T]GACTGTGCCCTCCTG | 84749 |
| rs758351063 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109029410 | TTTCTGTGTCTCTGT[C/G]TTGCTTATCTGGGAG | 84749 |
| rs758408043 | snp | G/T | | | missense | USP30 | GRCh38.p7 | 12:109084987 | CCCCAAAACACAGAT[G/T]TTTATGAATGGCGCC | 84749 |
| rs758474046 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109043975 | AGCAACCCGTGTCCA[C/T]CAACAAAAGAGTGGA | 84749 |
| rs758474789 | snp | C/G | 3.11105e-05 | 0.00394389 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052809 | GCCGGGACCAGGGTC[C/G]CCAGCTTGGGCCCGT | 84749 |
| rs758510507 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109065517 | GTGATCAGTGCTCCC[A/C]GTGTGGGGAAAAGTG | 84749 |
| rs758522884 | snp | A/G/T | 3.31188e-05 | 0.00406921 | missense, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088264 | CGTGGAGCCAGAACC[A/G/T]TCTTTCTCACGGGAA | 84749 |
| rs758577722 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109030774 | ACACCTGCCACCACG[C/T]CTGGCCAATTTTTGT | 84749 |
| rs758580089 | snp | C/T | 0.000313575 | 0.0125176 | synonymous-codon | USP30 | GRCh38.p7 | 12:109082893 | GAGCTGGTCCAGCCA[C/T]GGCACGCCTCTGAAG | 84749 |
| rs758600260 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109033957 | GTAGCTTGCTCAAAG[A/G]ACAAACTCCAAAAGT | 84749 |
| rs758622189 | snp | A/G | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | USP30, USP30-AS1 | GRCh38.p7 | 12:109052161 | AACAATAAGTTTGTT[A/G]GCTATTAAAGACGTT | 84749 |
| rs758650416 | snp | A/G | 1.64876e-05 | 0.00287116 | missense, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088310 | GCGTGTTGGTCGGGT[A/G]GTTCATCATTAGTAA | 84749 |
| rs758658163 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109039222 | CAGAAAGTTTTACAG[C/T]TTTAACTTTCAATTG | 84749 |
| rs758680895 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109073620 | AGAGTGGGCTGACAT[C/T]GGTCACTGGTGTTAG | 84749 |
| rs758704912 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109079835 | TTTTCCTTTACATCC[-/T]TGAGCATATTTATGA | 84749 |
| rs758749468 | in-del | -/CGCACACA | | | intron-variant | USP30 | GRCh38.p7 | 12:109081622 | ACACGCACGCATGCG[-/CGCACACA]CACACACACACACAC | 84749 |
| rs758836049 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109060278 | CCATTTTGGTATTGT[A/G]CAGTCATTGGTAATT | 84749 |
| rs758873759 | snp | G/T | 1.65831e-05 | 0.00287945 | missense | USP30 | GRCh38.p7 | 12:109084984 | GGCCCCCAAAACACA[G/T]ATTTTTATGAATGGC | 84749 |
| rs758882777 | snp | C/G | 8.71498e-05 | 0.00660055 | intron-variant, missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052732 | CGACAGGGCCATCCA[C/G]CGCTTCCTGCGGACC | 84749 |
| rs758919311 | snp | A/G | 1.66996e-05 | 0.00288956 | intron-variant | USP30 | GRCh38.p7 | 12:109073542 | CACCAGGTAAATACA[A/G]TACCAACACTTGATA | 84749 |
| rs758943698 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109063380 | TTCTGGGATTACAGG[C/T]GTGAGCCACCACGCC | 84749 |
| rs758953557 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109075271 | TTTTTGAGGAACCTT[C/G]ATACTGTTTTCCATT | 84749 |
| rs758993636 | snp | C/T | 1.66338e-05 | 0.00288386 | synonymous-codon | USP30 | GRCh38.p7 | 12:109085068 | CCCAGTTGTTCCCGA[C/T]TACAGGTGAGCCACC | 84749 |
| rs759007631 | snp | C/T | 3.33907e-05 | 0.00408586 | intron-variant | USP30 | GRCh38.p7 | 12:109072387 | ATAACACATAAGATG[C/T]GGACTTTTAAGATAT | 84749 |
| rs759083537 | snp | A/G | 1.64909e-05 | 0.00287144 | missense | USP30 | GRCh38.p7 | 12:109082919 | TGAAGCGGCATGAGC[A/G]CGTGCAGTTCAATGA | 84749 |
| rs759093393 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109078140 | TTTCCATAATAGCTG[C/T]ACCAGCCAGGTGCTG | 84749 |
| rs759130498 | snp | C/T | 1.65027e-05 | 0.00287247 | synonymous-codon | USP30 | GRCh38.p7 | 12:109085856 | GGTCCTGTCCTCCAG[C/T]GCCTACCTGCTGTTC | 84749 |
| rs759166181 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109049763 | GGAGGTTGCAGTGAG[A/C]CAAGATTGCGCCACT | 84749 |
| rs759178419 | snp | A/G | 1.65083e-05 | 0.00287296 | synonymous-codon | USP30 | GRCh38.p7 | 12:109071623 | ACAGGATGCTCACGA[A/G]TTATTCCATGTCATT | 84749 |
| rs759185457 | snp | A/G | 3.29647e-05 | 0.00405971 | synonymous-codon, missense, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088350 | GGCCAGCGGCAGCCT[A/G]ACCACCGCCACCCTC | 84749 |
| rs759198006 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109085163 | TGAATTAAGGAAAAT[A/G]TAGATGTTTATTTTT | 84749 |
| rs759277113 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109028508 | TTGAGATGTAGTTTC[C/T]CTCTTGTCGCCCAGA | 84749 |
| rs759277582 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109051139 | AAGCCATCCTCTCAC[C/G]TGGCCTCCCAAAGTG | 84749 |
| rs759281032 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109024577 | TGATTAATTTTAAGT[A/G]TCAACTTGGTGGGTT | 84749 |
| rs759311237 | snp | G/T | | | splice-acceptor-variant, intron-variant | USP30 | GRCh38.p7 | 12:109056681 | TTGTTTTCTTTTTTA[G/T]ATATAAAGTCATGAA | 84749 |
| rs759355521 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109034693 | TCTTCTGTCTAGTTG[C/T]TCTATCCATTATTGA | 84749 |
| rs759427249 | snp | A/G | 1.64939e-05 | 0.0028717 | missense, intron-variant | USP30 | GRCh38.p7 | 12:109056734 | ATTGCTGCTGCTCTT[A/G]CAGCAGGAATATATG | 84749 |
| rs759429392 | in-del | -/TTC | | | intron-variant | USP30 | GRCh38.p7 | 12:109036305 | TTAGTATTTCTTTCT[-/TTC]TTTTTTTTTTTTTTA | 84749 |
| rs759444479 | in-del | -/A | | | frameshift-variant | USP30 | GRCh38.p7 | 12:109085837 | GCAAGGCCAGCCTGC[-/A]GGAGGTCCTGTCCTC | 84749 |
| rs759495111 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109058253 | ACCAAGAGCCCAATA[G/T]ATACAAACAAGTATT | 84749 |
| rs759517107 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109036167 | CCTGTCTCAAAAAAT[A/C]TGTATATATTTATAC | 84749 |
| rs759521411 | snp | G/T | | | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022474 | CTTGAAAATCCAAAA[G/T]TGAATGTGTGCCAGG | 84749 |
| rs759566540 | in-del | -/T | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053973 | GACCAAGTTGGGCTC[-/T]TAGTTTCTTCTGCTA | 84749 |
| rs759587836 | snp | A/T | | | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109086534 | CAATTCTTTCTATGG[A/T]GTAAAGGCTCATCTG | 84749 |
| rs759608557 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109030606 | CACACACACAAAAAG[A/G]TAGGTTGCTTGTTTG | 84749 |
| rs759662917 | snp | C/G/T | 3.29779e-05 | 0.00406055 | missense, intron-variant | USP30 | GRCh38.p7 | 12:109058064 | ATCAGAAGGAGCCCC[C/G/T]CTCACACCAGTATTT | 84749 |
| rs759698574 | in-del | -/C | | | utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109027533 | ATCCTCCTGCCTCAG[-/C]CTCCCAAAGTGCTGG | 84749 |
| rs759717282 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109063245 | GCTGGGATGACAGGC[A/G]TGCACCACCACACCT | 84749 |
| rs759726160 | snp | C/G | 3.29533e-05 | 0.00405901 | intron-variant | USP30 | GRCh38.p7 | 12:109082034 | GGTATGCATTGAACC[C/G]CAAATGTCATCGCCA | 84749 |
| rs759727832 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109081254 | CAATATTAAACTGTT[G/T]CATAGTCACATATCT | 84749 |
| rs759762435 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109080290 | AGGATGCTGCTTTTC[A/G]CCACCCAGCACCACA | 84749 |
| rs759899100 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054185 | CTTTTGTGAACTCAC[A/G]TATCGTGTAAAAGCA | 84749 |
| rs759987051 | snp | C/T | 1.64751e-05 | 0.00287007 | synonymous-codon | USP30 | GRCh38.p7 | 12:109085814 | GTGGGTCTCCGATGA[C/T]ACTGTCCGCAAGGCC | 84749 |
| rs760008373 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon | USP30 | GRCh38.p7 | 12:109085697 | CTTCCGGCTGATGGC[A/G]GTTGTCGTCCACCAT | 84749 |
| rs760023763 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109068463 | GTTCTCTTGTTTTTG[C/T]TTTATTCTGAAGCCA | 84749 |
| rs760061896 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109038828 | GTGTGGTGGTATTAT[A/T]TAATGGTGTTAATTT | 84749 |
| rs760130939 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109047379 | AAAAACAAGAGCTAC[A/T]ACAAACAGTTCTGAC | 84749 |
| rs760239998 | snp | G/T | 3.75848e-05 | 0.00433486 | intron-variant | USP30 | GRCh38.p7 | 12:109071749 | CGTTCTGTGCAGCTT[G/T]TGCATATTTAATAAG | 84749 |
| rs760265083 | snp | A/G | 3.29522e-05 | 0.00405894 | missense | USP30 | GRCh38.p7 | 12:109085825 | ATGACACTGTCCGCA[A/G]GGCCAGCCTGCAGGA | 84749 |
| rs760265499 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109063248 | GGGATGACAGGCGTG[C/T]ACCACCACACCTGGC | 84749 |
| rs760292940 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109040070 | ATTAGAAAAATATTG[G/T]TTTTTTTCTACATGT | 84749 |
| rs760327509 | snp | C/T | 3.29712e-05 | 0.00406011 | missense | USP30 | GRCh38.p7 | 12:109071643 | TCCATGTCATTACCT[C/T]GTCATTGGAAGATGA | 84749 |
| rs760383938 | in-del | -/CT | 0.000362204 | 0.0134525 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109085965 | CTAGAGCTGATGGCA[-/CT]GTCTGCACTGTCCAG | 84749 |
| rs760391784 | snp | C/G | 1.64942e-05 | 0.00287173 | missense, intron-variant | USP30 | GRCh38.p7 | 12:109056741 | CTGCTCTTGCAGCAG[C/G]AATATATGTTATTTG | 84749 |
| rs760428592 | snp | A/G | 3.29815e-05 | 0.00406075 | missense, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088303 | TACCAGTGCGTGTTG[A/G]TCGGGTGGTTCATCA | 84749 |
| rs760446431 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109085256 | CTTTTAAATTAAAAA[-/T]TTTTAAAGTACATAA | 84749 |
| rs760452236 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109026119 | CTGGCTCTGTTGCCC[A/C]GGCTGGAGTGCAATG | 84749 |
| rs760531004 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109028574 | CCTCCACCTACCAGG[-/T]TCAGGCAATTATCCT | 84749 |
| rs760579495 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109033090 | AAAATGGCACTTAAT[G/T]TTTTAAAAAGAAGCC | 84749 |
| rs760617168 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109073686 | CCCCACTTTGGTCAG[-/T]TGTCAGCATGTCATT | 84749 |
| rs760644289 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109070631 | TGCTCTGGTGGCAGT[A/G]TGAGGGGACACCAAA | 84749 |
| rs760661832 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109049606 | TATCTCCTGAGGTCA[C/G]GAGTTCGAAACCAGC | 84749 |
| rs760664820 | snp | A/G | 9.91408e-05 | 0.00703993 | synonymous-codon | USP30 | GRCh38.p7 | 12:109085035 | GCCAACGCTGTCAGC[A/G]CCGATGCCCTTCCCT | 84749 |
| rs760684880 | snp | C/T | 3.29625e-05 | 0.00405958 | synonymous-codon, missense, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088356 | CGGCAGCCTGACCAC[C/T]GCCACCCTCCTGGAG | 84749 |
| rs760742072 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109047005 | GCCCGGCCAGCTGGA[A/G]GTTTTGATCCAGACC | 84749 |
| rs760768893 | in-del | -/T | 0.0107192 | 0.0724204 | intron-variant | USP30 | GRCh38.p7 | 12:109072282 | AAGGTTTTCAGTCTG[-/T]TTTTTTTTTTTCTCC | 84749 |
| rs760810199 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109071495 | TGAGCTGGGCCTTGA[A/G]AAGGTAGAAAGCAAA | 84749 |
| rs760825546 | snp | A/C | 3.30814e-05 | 0.00406689 | synonymous-codon | USP30 | GRCh38.p7 | 12:109072346 | AATTACCTGCCGCAC[A/C]AGAGGTAGCTGTTTT | 84749 |
| rs760832834 | snp | A/C | | | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022281 | TGATCCATGATGGCA[A/C]CTGGCAAAAGCTATG | 84749 |
| rs760848440 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109023536 | CTCCAGCCTGGGTGA[C/T]AGAGCGAAACTCTGT | 84749 |
| rs760866911 | snp | A/G | | | synonymous-codon, intron-variant | USP30 | GRCh38.p7 | 12:109058074 | GCCCCCCTCACACCA[A/G]TATTTATCCTTAACA | 84749 |
| rs760915912 | snp | C/T | 1.6486e-05 | 0.00287102 | intron-variant | USP30 | GRCh38.p7 | 12:109082056 | TCATCGCCAGCTGGC[C/T]TGTGTGTGCTGATGT | 84749 |
| rs760981398 | snp | A/C | 1.69882e-05 | 0.00291441 | intron-variant | USP30 | GRCh38.p7 | 12:109084937 | TTTCATTGACTCGGG[A/C]CTTTTTCTCTTGCAG | 84749 |
| rs761036791 | snp | A/C | 1.65162e-05 | 0.00287365 | missense, intron-variant | USP30 | GRCh38.p7 | 12:109058073 | AGCCCCCCTCACACC[A/C]GTATTTATCCTTAAC | 84749 |
| rs761041036 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109069837 | GAGGTGAGGTTTCAG[C/T]GGAGACCGGAAGTAT | 84749 |
| rs761052062 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109028773 | TGAGCCACCACACCC[A/G]ACTACCACACACTTT | 84749 |
| rs761081189 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109080217 | CTTCCTGGCATTTCC[C/T]CTGGTCTCTCCACCA | 84749 |
| rs761088154 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109080953 | ACAATGATGACATCA[C/T]CTAAGGATGCATTTC | 84749 |
| rs761095129 | snp | A/G | 1.69315e-05 | 0.00290955 | missense | USP30 | GRCh38.p7 | 12:109085893 | CGCGTCCTTTCCAGG[A/G]TGCAGCACCAGAGCC | 84749 |
| rs761124569 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109044931 | GATGGGGGAAAAAAT[C/G]TTTTCTGATTATAGT | 84749 |
| rs761218952 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109030772 | AGACACCTGCCACCA[C/T]GCCTGGCCAATTTTT | 84749 |
| rs761219730 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109030311 | ACCTGCAGGTCTATT[A/G]TGTGGATTAAACAAG | 84749 |
| rs761237005 | snp | C/T | 1.65244e-05 | 0.00287436 | synonymous-codon | USP30 | GRCh38.p7 | 12:109072334 | AACTCCCAAACAAAT[C/T]ACCTGCCGCACAAGA | 84749 |
| rs761254814 | snp | A/G | | | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109087201 | CCTATGTTTTAAGCT[A/G]TATTTTTAATTTAGA | 84749 |
| rs761312384 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109066064 | CAAGACCAGCCTGGG[A/C]AACATGGTGAAACTC | 84749 |
| rs761394592 | snp | C/G | 7.01951e-05 | 0.0059239 | missense | USP30 | GRCh38.p7 | 12:109085910 | GCAGCACCAGAGCCA[C/G]GAGTGCAAGTCTGAA | 84749 |
| rs761397419 | snp | C/T | 1.95463e-05 | 0.00312615 | intron-variant | USP30 | GRCh38.p7 | 12:109082630 | CTGTCCTATTTTAGG[C/T]ATTGCTGCAGAGAAA | 84749 |
| rs761397903 | snp | C/T | 1.7505e-05 | 0.00295841 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052663 | GAGACGGTTTCAGGC[C/T]TCCGGTGCGGCTGCA | 84749 |
| rs761457590 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109032781 | AACCCCTATTAAATT[A/G]CACACTTTAAAGGCA | 84749 |
| rs761459652 | snp | G/T | 1.74461e-05 | 0.00295343 | utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088203 | AAACTGTTAAAAATG[G/T]TTTTATTTTTTAGTA | 84749 |
| rs761460531 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109073261 | TGTGTAAATTCTCCT[A/G]TGAAGGAATGGGATG | 84749 |
| rs761520983 | snp | C/T | | | utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109024892 | CCAAAGTGCTGGGAT[C/T]ACAGGCGTGAACCAC | 84749 |
| rs761527492 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109025957 | CCAAAGGTGCTGGCA[C/T]TACAGGTGTGAGCCA | 84749 |
| rs761572473 | snp | C/T | 1.64914e-05 | 0.00287149 | synonymous-codon | USP30 | GRCh38.p7 | 12:109082950 | GTTCCTGATGATGGA[C/T]ATTTACAAGTACCAC | 84749 |
| rs761592234 | snp | C/T | | | missense, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088327 | TTCATCATTAGTAAG[C/T]TCCCGTGGGCCAGCG | 84749 |
| rs761609564 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109038681 | TTTATGTTTCTCTTT[A/G]TATGAATCTGCCAAA | 84749 |
| rs761692871 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109059595 | CTCAGCTCACTGCAA[C/G]CTCCGCCTCCCGGGT | 84749 |
| rs761717706 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046822 | CCACCTCAGCCTCCC[A/G]AGTAGCTAGGATTAC | 84749 |
| rs761743754 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109047861 | CTAGACTAATTTTAG[G/T]ATTCACCCAGCCAGC | 84749 |
| rs761750113 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109084056 | TTGAGAGCATGCTGG[C/T]TGTGGTTAAAGATGC | 84749 |
| rs761764202 | snp | A/G | 1.67919e-05 | 0.00289753 | intron-variant | USP30 | GRCh38.p7 | 12:109072257 | TGAGGGTGGTGAAAG[A/G]GATTATAGTAAGGTT | 84749 |
| rs761764211 | snp | A/G | 1.64969e-05 | 0.00287196 | synonymous-codon, intron-variant | USP30 | GRCh38.p7 | 12:109057951 | TGGCCTTGTTAATTT[A/G]GGGAACACCTGCTTC | 84749 |
| rs761791119 | in-del | -/TTG | | | intron-variant | USP30 | GRCh38.p7 | 12:109056179 | TTGACTTAGTTTTTG[-/TTG]TTGTTGTTGTTGTTG | 84749 |
| rs761923280 | snp | A/C | 1.65787e-05 | 0.00287907 | missense | USP30 | GRCh38.p7 | 12:109073525 | TCTGCAAACACTGTG[A/C]ACACCAGGTAAATAC | 84749 |
| rs761929708 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109068828 | TGAACACGTCTGTCC[A/G]GTGGCCTTTTTCTCT | 84749 |
| rs761955302 | in-del | -/GCAC | 1.6473e-05 | 0.00286988 | frameshift-variant | USP30 | GRCh38.p7 | 12:109085720 | CCACCATGGAGACAT[-/GCAC]GCACTCTGGACACTT | 84749 |
| rs761961429 | snp | C/T | 1.64808e-05 | 0.00287057 | intron-variant | USP30 | GRCh38.p7 | 12:109085657 | CCTGACATGTGTTCG[C/T]ATCATTCAGCTCCTC | 84749 |
| rs761981428 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109034322 | TTTCATTCCATTGCA[A/G]TTAGAGAACATATTT | 84749 |
| rs762039081 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109076732 | GTGATTGATTTTTTC[-/T]TTTTTTTTTTTTTTT | 84749 |
| rs762051136 | snp | G/T | 1.65787e-05 | 0.00287907 | missense | USP30 | GRCh38.p7 | 12:109085060 | TTCCCTCTCCCAGTT[G/T]TTCCCGACTACAGGT | 84749 |
| rs762068937 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053096 | GCCTCCTAGGCCTGC[C/T]AAGACCCCTCAATCC | 84749 |
| rs762144294 | snp | C/T | 1.64789e-05 | 0.0028704 | intron-variant | USP30 | GRCh38.p7 | 12:109067521 | TACCTTTTTTGTTTC[C/T]AGCCTTGTCCTGCCA | 84749 |
| rs762224642 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109028606 | CCTCAGCCTTCTGAG[C/T]AGCTGAGATTACAGG | 84749 |
| rs762271213 | snp | G/T | 1.65026e-05 | 0.00287246 | intron-variant | USP30 | GRCh38.p7 | 12:109067654 | ATTTGAACAGGTTTA[G/T]CTTGGAGAATCCTTT | 84749 |
| rs762360693 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109043469 | AGAGTACCAATACGA[C/T]TGAATGGGAAAAGGA | 84749 |
| rs762361819 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109080173 | GTTTAGGTATAAACT[C/T]TGGGGCTCATCCCCT | 84749 |
| rs762499302 | snp | A/G | 1.65081e-05 | 0.00287293 | synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088284 | TCTCACGGGAAGACT[A/G]TGGTACCAGTGCGTG | 84749 |
| rs762521648 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109065881 | CCTGAAATGTTATTT[A/T]CTTTTTACATCTATG | 84749 |
| rs762546878 | snp | A/G | 0.000115313 | 0.0075923 | missense, utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109067551 | AAGAAGTTACTGATG[A/G]TGAGGTCTTAGATGC | 84749 |
| rs762563369 | snp | C/T | | | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109086902 | ACTATGGGGCTGCAG[C/T]CTCTCTGAACCTCAG | 84749 |
| rs762622050 | snp | A/G | 8.36659e-05 | 0.0064673 | intron-variant | USP30 | GRCh38.p7 | 12:109082835 | CCCGATTTCTCTTCC[A/G]CCCGCAGCTCCCTCA | 84749 |
| rs762624099 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109059309 | AAGTGATTCTTGTGC[C/T]TCAGCCTCCTGAGTA | 84749 |
| rs762632652 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109072897 | CTATCCCAATTTTCC[A/G]CACACTGAGGCTTGT | 84749 |
| rs762654088 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109085488 | ATACATATACTCATA[C/G]AATGTACATCTTGCC | 84749 |
| rs762655701 | in-del | -/ACCTCATTCTTTTATATG | | | intron-variant | USP30 | GRCh38.p7 | 12:109027721 | GTAGCATCTATCAGA[-/ACCTCATTCTTTTATATG]ACTGAATAATATTTC | 84749 |
| rs762681706 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109037989 | CCCCTGAATATCTGA[A/T]TCCTCAGATTTTCTT | 84749 |
| rs762756225 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109024365 | CAGGCTCAAGCCATC[A/C]TCCCACCTCAGCCTC | 84749 |
| rs762805974 | snp | C/T | 0.000136558 | 0.00826199 | intron-variant | USP30 | GRCh38.p7 | 12:109084933 | TAATTTTCATTGACT[C/T]GGGCCTTTTTCTCTT | 84749 |
| rs762816250 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109077851 | GGTGTGTGTGAGAGA[-/T]TACGTTATGCAGTTT | 84749 |
| rs762888536 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109060972 | TTTAAAAAAATAGAG[A/G]TGGGGTCTTGCTATG | 84749 |
| rs762896548 | snp | C/T | 7.16358e-05 | 0.00598438 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052671 | TTCAGGCCTCCGGTG[C/T]GGCTGCAATGCTGAG | 84749 |
| rs762905623 | in-del | -/A | | | intron-variant | USP30 | GRCh38.p7 | 12:109071841 | GGTGGGAATGAGGCC[-/A]GGGGAGGGTCTTAAA | 84749 |
| rs762914614 | snp | C/T | | | utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109024840 | TAGCCAGGATGGTCT[C/T]GATCTCCTGATCTCG | 84749 |
| rs762923893 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109045344 | CTCTTTAGCCCATTC[C/T]CAGGTGTTAATGAGA | 84749 |
| rs762925112 | in-del | -/TTTA | | | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109086777 | GGTTACTTTCATCTG[-/TTTA]TTTATTGCCCATGCA | 84749 |
| rs763033659 | snp | C/T | | | missense | USP30 | GRCh38.p7 | 12:109081338 | ATTTCTTTCAGAGTC[C/T]TGTTCGATTTGATAC | 84749 |
| rs763048810 | snp | A/T | 1.66374e-05 | 0.00288417 | intron-variant | USP30 | GRCh38.p7 | 12:109057918 | TCTTCCCCCTGCTTT[A/T]TTTTTAGGGCTTGTG | 84749 |
| rs763070142 | snp | A/G | 6.6107e-05 | 0.00574884 | missense, intron-variant | USP30 | GRCh38.p7 | 12:109056773 | GGTCCCATTACAGAA[A/G]GAAAGAAGCGTAGAA | 84749 |
| rs763092848 | in-del | -/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109083940 | AAAAGAGATGAGGTA[-/G]GGGGACAGACTCTGG | 84749 |
| rs763101057 | snp | C/G | 1.64814e-05 | 0.00287061 | missense, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088365 | GACCACCGCCACCCT[C/G]CTGGAGGGGCTTTTC | 84749 |
| rs763107450 | snp | A/G/T | 3.29882e-05 | 0.00406118 | intron-variant | USP30 | GRCh38.p7 | 12:109081889 | AACAGTTTCAGTATA[A/G/T]CTGTCCTTTGAATTG | 84749 |
| rs763111128 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109068782 | GCAGTCACTGAGCCC[A/C]CATCGTGCTGTAGTC | 84749 |
| rs763140130 | in-del | -/CACA | | | intron-variant | USP30 | GRCh38.p7 | 12:109081628 | ACGCATGCGCGCACA[-/CACA]CACACACACACACAC | 84749 |
| rs763179103 | snp | G/T | 0.000115406 | 0.00759537 | missense | USP30 | GRCh38.p7 | 12:109085800 | AGCAATCAGTGGCTG[G/T]GGGTCTCCGATGACA | 84749 |
| rs763195204 | snp | C/T | 1.64776e-05 | 0.00287028 | intron-variant | USP30 | GRCh38.p7 | 12:109081324 | GGATTTTCTGCAATA[C/T]TTCTTTCAGAGTCCT | 84749 |
| rs763267961 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109032869 | CCAGATGGGTTTTAT[G/T]TCACACCAGAGCAAT | 84749 |
| rs763271779 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054322 | GCTCAGGAGTTCGAG[A/G]CCAGCCTGGGCAATG | 84749 |
| rs763273391 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109070227 | GGCTCAGACTGGGGT[C/T]GAAGCAGGGTAGCTG | 84749 |
| rs763299555 | in-del | -/GCCT | 1.65027e-05 | 0.00287247 | frameshift-variant | USP30 | GRCh38.p7 | 12:109085856 | GTCCTGTCCTCCAGC[-/GCCT]GCCTACCTGCTGTTC | 84749 |
| rs763299821 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109041348 | CATGATTTAAGAAAA[C/T]GAATATGGCCAGGTG | 84749 |
| rs763303470 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109068676 | GTCACCAAGGACATC[A/C]GATAACTTTTTTAAG | 84749 |
| rs763311544 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109031825 | ACAGAAGGTAGAGAC[A/G]AGGTGTGATTACTCG | 84749 |
| rs763315802 | snp | A/C | 1.65239e-05 | 0.00287431 | intron-variant | USP30 | GRCh38.p7 | 12:109067666 | TTAGCTTGGAGAATC[A/C]TTTCCCCTAGTGACT | 84749 |
| rs763359194 | in-del | -/TTTCT | 1.64727e-05 | 0.00286986 | frameshift-variant | USP30 | GRCh38.p7 | 12:109072348 | TACCTGCCGCACAAG[-/TTTCT]AGGTAGCTGTTTTCC | 84749 |
| rs763485437 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon | USP30 | GRCh38.p7 | 12:109085682 | CTCCTCCACATACCT[C/T]TTCCGGCTGATGGCA | 84749 |
| rs763569820 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109040428 | TTGCTCCTGCTATAG[A/T]AGTTCTCTACTGCTG | 84749 |
| rs763659754 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109035198 | GTCTTTTTTGCTCCT[C/T]AGCTCCTCCATTACT | 84749 |
| rs763671633 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109036455 | ACAGGTGTGAACCAC[A/G]CCCAGCTAATTTTTG | 84749 |
| rs763695829 | snp | A/G | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | USP30, USP30-AS1 | GRCh38.p7 | 12:109051753 | TTTTGTATTTTTAGT[A/G]GAGATGGGGTTTCAC | 84749 |
| rs763697205 | snp | C/T | | | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109087116 | AGTATATATTGAGCA[C/T]TTTCTTCCCTTTTCA | 84749 |
| rs763705550 | snp | C/T | 1.71237e-05 | 0.00292602 | missense | USP30 | GRCh38.p7 | 12:109085899 | CTTTCCAGGATGCAG[C/T]ACCAGAGCCAGGAGT | 84749 |
| rs763711765 | snp | C/T | 1.64746e-05 | 0.00287002 | synonymous-codon | USP30 | GRCh38.p7 | 12:109081942 | CTGTAGGGTCACCCA[C/T]TGACCCTGGACCACT | 84749 |
| rs763748614 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109065917 | TTTTGTGCTGCAGTG[A/G]CAGAGTTGAGTAGTT | 84749 |
| rs763795502 | snp | C/G | 3.29527e-05 | 0.00405898 | missense | USP30 | GRCh38.p7 | 12:109085826 | TGACACTGTCCGCAA[C/G]GCCAGCCTGCAGGAG | 84749 |
| rs763881633 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109059435 | TCCTGGCCTCAAGTG[A/G]TATGCCTGCCTCAGC | 84749 |
| rs763900031 | snp | C/T | 1.65545e-05 | 0.00287697 | stop-gained | USP30 | GRCh38.p7 | 12:109082870 | CTCTGCATCCACCTA[C/T]AGCGGCTGAGCTGGT | 84749 |
| rs763962300 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109061085 | CCACTGCACCCAGCC[A/T]TGTTCATGGGAGTTA | 84749 |
| rs764006106 | in-del | -/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109028770 | GCATGAGCCACCACA[-/C]CCGACTACCACACAC | 84749 |
| rs764042226 | snp | C/T | 1.69255e-05 | 0.00290903 | intron-variant | USP30 | GRCh38.p7 | 12:109084942 | TTGACTCGGGCCTTT[C/T]TCTCTTGCAGTTCTG | 84749 |
| rs764115252 | snp | A/C | 1.64841e-05 | 0.00287085 | stop-gained | USP30 | GRCh38.p7 | 12:109071646 | ATGTCATTACCTCGT[A/C]ATTGGAAGATGAGCG | 84749 |
| rs764122377 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046597 | GCCACTTTGGCCTAG[C/T]CAAAGTTGACAATTA | 84749 |
| rs764227588 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109063598 | CAAATGGTAATTCTG[A/T]TTAATTTTTTGAGGA | 84749 |
| rs764260156 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109031882 | GCCAAGGCAGGAGGA[C/T]TGCTTGAGCTCAGGA | 84749 |
| rs764302950 | snp | C/G | 1.64727e-05 | 0.00286986 | missense | USP30 | GRCh38.p7 | 12:109072350 | ACCTGCCGCACAAGA[C/G]GTAGCTGTTTTCCAT | 84749 |
| rs764315539 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109066673 | CTGGGCGACAGAGCA[C/T]GACTCTGTTTCAAAA | 84749 |
| rs764329270 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109068796 | CACATCGTGCTGTAG[G/T]CTGCAGGAAAAAGAG | 84749 |
| rs764346587 | in-del | -/AA | | | intron-variant | USP30 | GRCh38.p7 | 12:109061394 | CTCTAACTTTGGTTT[-/AA]AAAAAAAAAAAAAAA | 84749 |
| rs764359520 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109040490 | TTAAAAAAATTAACA[A/G]TTGTTATCCCACACA | 84749 |
| rs764363175 | snp | A/C | 1.65146e-05 | 0.0028735 | missense | USP30 | GRCh38.p7 | 12:109073503 | GGAAGACTCACTAGT[A/C]ATATGGTCTGCAAAC | 84749 |
| rs764380232 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109047760 | TGGGAGGCCAAGGTG[A/G]GTGGATCACTTGAGC | 84749 |
| rs764391497 | snp | A/C/G | 4.96285e-05 | 0.00498118 | missense | USP30 | GRCh38.p7 | 12:109085051 | CCGATGCCCTTCCCT[A/C/G]TCCCAGTTGTTCCCG | 84749 |
| rs764435639 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055930 | TCAAGGGGACAAGGA[C/T]AGGTCCCACTGATAT | 84749 |
| rs764490681 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054382 | TAAAAATTACCTGGG[C/T]ATGTGGTGTGCAGCT | 84749 |
| rs764530993 | in-del | -/AG | | | intron-variant | USP30 | GRCh38.p7 | 12:109060442 | AGCTCTGCTTGACAC[-/AG]AAATCTTTATGAAGC | 84749 |
| rs764611080 | in-del | -/T | 1.6806e-05 | 0.00289875 | frameshift-variant, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088226 | TTTTAGTAAGCAAAA[-/T]TTTACGAAAAGTCAG | 84749 |
| rs764618361 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109027335 | CCAGGTTGACGTGCA[A/G]TGATGCAATCACGGC | 84749 |
| rs764662962 | snp | A/G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109077390 | TTATTGGATACAAGC[A/G/T]TATGTATTATGATGA | 84749 |
| rs764672926 | snp | G/T | 1.65312e-05 | 0.00287495 | missense, intron-variant | USP30 | GRCh38.p7 | 12:109058075 | CCCCCCTCACACCAG[G/T]ATTTATCCTTAACAC | 84749 |
| rs764733800 | snp | C/T | 1.73141e-05 | 0.00294223 | splice-acceptor-variant, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088514 | AGCCATCTTTATACC[C/T]GCAATGAGAAAACAA | 84749 |
| rs764751481 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109084580 | GGACAGCCCCCGCAA[A/C]AAAGAATGATCCAGC | 84749 |
| rs764760313 | in-del | -/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109031799 | GGTCTCAAAAGTAGT[-/C]ACTCATAGAAACAGA | 84749 |
| rs764816663 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109049813 | AGAGTGAGGCATTAT[G/T]GCAAAAAAGAAAAGA | 84749 |
| rs764856358 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109063381 | TCTGGGATTACAGGC[A/G]TGAGCCACCACGCCA | 84749 |
| rs764858696 | snp | A/G | 6.64717e-05 | 0.00576467 | synonymous-codon | USP30 | GRCh38.p7 | 12:109082737 | TAAACAGTTAAAACT[A/G]GGGAAGGTGAGCCCA | 84749 |
| rs764875261 | snp | A/G | 3.86757e-05 | 0.00439731 | intron-variant | USP30 | GRCh38.p7 | 12:109082631 | TGTCCTATTTTAGGC[A/G]TTGCTGCAGAGAAAT | 84749 |
| rs764892017 | snp | C/T | 3.49822e-05 | 0.00418209 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052666 | ACGGTTTCAGGCCTC[C/T]GGTGCGGCTGCAATG | 84749 |
| rs765006901 | snp | C/T | | | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022494 | TGTGTGCCAGGCACC[C/T]GGATATGTACTTCAC | 84749 |
| rs765022234 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109071758 | CAGCTTGTGCATATT[C/T]AATAAGTATAGGGGA | 84749 |
| rs765089502 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109085164 | GAATTAAGGAAAATA[C/T]AGATGTTTATTTTTC | 84749 |
| rs765103324 | snp | C/T | 3.35076e-05 | 0.004093 | intron-variant | USP30 | GRCh38.p7 | 12:109072263 | TGGTGAAAGGGATTA[C/T]AGTAAGGTTTTCAGT | 84749 |
| rs765111163 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046093 | TGGGGGAAGTCAGTC[-/TT]TTTTTTTTTTTTTTT | 84749 |
| rs765168208 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109024148 | GGGGATCAATAACCA[C/T]AACTACTTCATAGGG | 84749 |
| rs765191370 | snp | C/T | 3.31807e-05 | 0.00407299 | synonymous-codon | USP30 | GRCh38.p7 | 12:109073529 | CAAACACTGTGAACA[C/T]CAGGTAAATACAATA | 84749 |
| rs765226169 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109029341 | GCACTCTCTCTGACA[A/G]ACTAAAAGTTTTTAA | 84749 |
| rs765247896 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109080321 | TCAACCAGGAAAAAA[A/T]GCCACAAACACACAA | 84749 |
| rs765292681 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109058264 | AATAGATACAAACAA[C/G]TATTTTTTAAAAATC | 84749 |
| rs765393610 | snp | G/T | 6.03227e-05 | 0.00549161 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052805 | AGAGGCCGGGACCAG[G/T]GTCCCCAGCTTGGGC | 84749 |
| rs765452005 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052904 | GTCCTTTAGGGTTGG[A/G]GGCCTGGGCCCGTAG | 84749 |
| rs765453378 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109059237 | CTCACCTTTTTTTCC[C/T]AGCCTGGAGTGCAGT | 84749 |
| rs765475985 | snp | A/G | 4.94654e-05 | 0.00497295 | missense, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088306 | CAGTGCGTGTTGGTC[A/G]GGTGGTTCATCATTA | 84749 |
| rs765477620 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109066386 | TGATTCTACCTGTGA[C/T]TGAAAAGTAAACCAC | 84749 |
| rs765510876 | snp | G/T | 1.6483e-05 | 0.00287076 | intron-variant | USP30 | GRCh38.p7 | 12:109081310 | CCTAAATCGTTTCTG[G/T]ATTTTCTGCAATATT | 84749 |
| rs765545048 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109072855 | AACTCTACAAAGTTG[A/G]TGATACTGGAGTTAA | 84749 |
| rs765636960 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109077331 | TGTTTGCTAAAATTT[A/G]TCTTTTCTTTAGCTC | 84749 |
| rs765654524 | in-del | -/AG | | | intron-variant | USP30 | GRCh38.p7 | 12:109037911 | TTACCCTGAGCATGT[-/AG]AGAGTGCTGCACATG | 84749 |
| rs765685392 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109038884 | TGACCATCTTTTCAT[A/G]TGCCTACTGATCATT | 84749 |
| rs765744875 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109077115 | TGTTTTTATATATTA[C/T]TGAATTTGATTTGCT | 84749 |
| rs765837950 | in-del | -/TT | 0.00175488 | 0.0295696 | intron-variant | USP30 | GRCh38.p7 | 12:109072282 | AAGGTTTTCAGTCTG[-/TT]TTTTTTTTTTCTCCC | 84749 |
| rs765877174 | snp | A/G | 3.33578e-05 | 0.00408384 | intron-variant | USP30 | GRCh38.p7 | 12:109082757 | AGGTGAGCCCACACT[A/G]CACACCCTGTTGGCT | 84749 |
| rs765948598 | snp | C/T | 8.35722e-05 | 0.00646368 | intron-variant | USP30 | GRCh38.p7 | 12:109082838 | GATTTCTCTTCCACC[C/T]GCAGCTCCCTCAGTG | 84749 |
| rs765975371 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109063290 | ATTTTTAGTAGAGAC[A/G]GGGTTTTACCACATT | 84749 |
| rs766072201 | snp | G/T | 3.29473e-05 | 0.00405864 | missense, utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109067556 | GTTACTGATGATGAG[G/T]TCTTAGATGCAAGCT | 84749 |
| rs766156673 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109049612 | CTGAGGTCAGGAGTT[C/T]GAAACCAGCCTGGCC | 84749 |
| rs766156788 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109033182 | CAGAGTCAAATAAAA[C/T]ATAGAGGTGAACCTC | 84749 |
| rs766181925 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109031149 | ATATTTTATAGAACT[A/C]GATAAACATGTTCAA | 84749 |
| rs766208516 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109048286 | GACAGGGTTTCACCA[C/T]GTTGCCCAGACTCGT | 84749 |
| rs766237465 | snp | A/G | 1.73963e-05 | 0.00294921 | intron-variant, missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052679 | TCCGGTGCGGCTGCA[A/G]TGCTGAGCTCCCGGG | 84749 |
| rs766260374 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109084384 | GTATTCCTTAGAAGC[C/T]GACAGAATTAAAGCA | 84749 |
| rs766278965 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109083207 | ACAGCAGGATTGGGG[A/G]TGGAAGAGGGAAGAT | 84749 |
| rs766314802 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109034516 | AGGATCGCTTGAGCT[C/T]ATGAGTTCAAGACCA | 84749 |
| rs766332332 | snp | C/T | 2.78664e-05 | 0.00373262 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052778 | TGAGATTTTGGGGGG[C/T]GGGGCTGCCGAAGAG | 84749 |
| rs766365931 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109042167 | ATTGTATTAGCTGAC[C/T]TTCTTTTTTCACTTT | 84749 |
| rs766413059 | snp | A/G | 1.65351e-05 | 0.00287528 | synonymous-codon, intron-variant | USP30 | GRCh38.p7 | 12:109056775 | TCCCATTACAGAAAG[A/G]AAGAAGCGTAGAAAA | 84749 |
| rs766421493 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109056181 | GACTTAGTTTTTGTT[G/T]TTGTTGTTGTTGTTG | 84749 |
| rs766477757 | snp | G/T | 3.52715e-05 | 0.00419935 | intron-variant | USP30 | GRCh38.p7 | 12:109058160 | TTTCAAAGAAGTCCA[G/T]ATGACAGAGACTCTT | 84749 |
| rs766480110 | snp | A/G | 1.89446e-05 | 0.00307765 | synonymous-codon | USP30 | GRCh38.p7 | 12:109085930 | GCAAGTCTGAAGAAT[A/G]ACTGTGCCCTCCTGC | 84749 |
| rs766553981 | snp | A/G | 1.65181e-05 | 0.00287381 | missense, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088456 | ATGGGGCTCCCAGGG[A/G]CCAGTTCTCTTTCAT | 84749 |
| rs766607836 | in-del | -/ATG | 3.37325e-05 | 0.00410672 | intron-variant | USP30 | GRCh38.p7 | 12:109072401 | GTGGACTTTTAAGAT[-/ATG]ATAATAATTTGCTTG | 84749 |
| rs766619015 | snp | C/T | 1.64879e-05 | 0.00287118 | missense | USP30 | GRCh38.p7 | 12:109071666 | GAAGATGAGCGAGAC[C/T]GCCAGCCTCGGGTCA | 84749 |
| rs766714160 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109080229 | TCCCCTGGTCTCTCC[A/G]CCAGCCCTGATTCTT | 84749 |
| rs766715671 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109030327 | TGTGGATTAAACAAG[A/C]TGATGGATATTCATG | 84749 |
| rs766733453 | snp | A/T | 1.66277e-05 | 0.00288333 | intron-variant | USP30 | GRCh38.p7 | 12:109057920 | TTCCCCCTGCTTTTT[A/T]TTTAGGGCTTGTGCC | 84749 |
| rs766737671 | in-del | -/TT | | | intron-variant | USP30 | GRCh38.p7 | 12:109056200 | TTGTTGTTGTTGTTG[-/TT]GTTTTTTATGAGACT | 84749 |
| rs766775914 | in-del | -/C | 1.9812e-05 | 0.00314732 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109085941 | GAATGACTGTGCCCT[-/C]CTGCAAGGCTAGAGC | 84749 |
| rs766792013 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109072521 | AAATAGATTCTCTTG[A/G]TGTTCCCTTGCACCC | 84749 |
| rs766793094 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109026957 | TTTTCTTATAAGGGC[A/G]CTATCTCATCATGTC | 84749 |
| rs766807132 | snp | A/G | 1.67632e-05 | 0.00289505 | intron-variant | USP30 | GRCh38.p7 | 12:109085090 | TGAGCCACCCTTTAC[A/G]AGCCCCATCTTAGAG | 84749 |
| rs766818745 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109069944 | GATGGTTATAAAGCT[G/T]CCACCTGTGGAGAAT | 84749 |
| rs766920869 | snp | A/G | 1.64732e-05 | 0.0028699 | missense | USP30 | GRCh38.p7 | 12:109085687 | CCACATACCTCTTCC[A/G]GCTGATGGCAGTTGT | 84749 |
| rs766933568 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109067306 | TTATTTTTAGTGGAG[A/G]CGGAGTTTCACCATG | 84749 |
| rs767058032 | snp | G/T | | | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109087292 | AAAAGGTCATCTGAG[G/T]TAAGGCTAAGACCGC | 84749 |
| rs767058503 | snp | C/G | 1.64765e-05 | 0.00287019 | missense | USP30 | GRCh38.p7 | 12:109085701 | CGGCTGATGGCAGTT[C/G]TCGTCCACCATGGAG | 84749 |
| rs767060403 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109077853 | TGTGTGTGAGAGATT[A/G]CGTTATGCAGTTTTA | 84749 |
| rs767080885 | snp | C/T | | | utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109025046 | CAAATCAGCTAGAGG[C/T]CCAGACAGAACAGAA | 84749 |
| rs767089295 | snp | A/G | 1.64953e-05 | 0.00287182 | missense | USP30 | GRCh38.p7 | 12:109071631 | CTCACGAATTATTCC[A/G]TGTCATTACCTCGTC | 84749 |
| rs767094298 | snp | C/T | 3.29826e-05 | 0.00406082 | synonymous-codon | USP30 | GRCh38.p7 | 12:109082920 | GAAGCGGCATGAGCA[C/T]GTGCAGTTCAATGAG | 84749 |
| rs767122892 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109038731 | ATTTTACATTCCTGC[C/T]AGCAACGTATGATAT | 84749 |
| rs767178066 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109036826 | ATACCTTTTATGTGA[A/G]GGTTGCTTCTCTCTG | 84749 |
| rs767189678 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109059686 | GCCCGGCTAATGTTT[A/G]TATTTTTAGTAGAGA | 84749 |
| rs767190070 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109074871 | TGCATCTTTGAGCAA[C/T]ATCTCCCCACCTCCC | 84749 |
| rs767320009 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109032996 | CTGAAAATAAAAAGC[A/G]TGTGCTATGTACAAG | 84749 |
| rs767353367 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109058229 | TACAGATCATTATGA[A/G]TAAACAACACCAAGA | 84749 |
| rs767354931 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109028089 | AGTGGGTGTGGAGTG[G/T]TCTGATTTGCATTTC | 84749 |
| rs767430755 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054496 | ACTGCACTCCAGCCT[A/G]GGCACTAGAGCAACT | 84749 |
| rs767441525 | in-del | -/AAGCT | | | intron-variant | USP30 | GRCh38.p7 | 12:109060032 | CTCATCAGACCTCGG[-/AAGCT]AAGCCGGGTAGTGGT | 84749 |
| rs767452907 | snp | A/G | 5.00964e-05 | 0.00500457 | stop-gained, synonymous-codon, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088478 | CTCTTTCATCATCTC[A/G]GTGCTCCCCGATGTG | 84749 |
| rs767537858 | snp | A/G | 1.66183e-05 | 0.00288251 | missense | USP30 | GRCh38.p7 | 12:109082850 | ACCCGCAGCTCCCTC[A/G]GTGTCTCTGCATCCA | 84749 |
| rs767552474 | in-del | -/TGCG | | | intron-variant | USP30 | GRCh38.p7 | 12:109081618 | ATACACACGCACGCA[-/TGCG]CGCACACACACACAC | 84749 |
| rs767625958 | snp | A/C | 1.6708e-05 | 0.00289028 | intron-variant | USP30 | GRCh38.p7 | 12:109082762 | AGCCCACACTACACA[A/C]CCTGTTGGCTTTGTT | 84749 |
| rs767665632 | in-del | -/TG | | | intron-variant | USP30 | GRCh38.p7 | 12:109048733 | AACAGAGTGAGACTC[-/TG]TGTCTCAAAAAAAAA | 84749 |
| rs767700973 | snp | C/T | 3.34829e-05 | 0.00409149 | intron-variant | USP30 | GRCh38.p7 | 12:109072280 | GTAAGGTTTTCAGTC[C/T]GTTTTTTTTTTTTCT | 84749 |
| rs767720874 | snp | A/G | 1.64757e-05 | 0.00287012 | missense | USP30 | GRCh38.p7 | 12:109081373 | GATAGCCTTTCACTA[A/G]GTATTCCAGCCGCCA | 84749 |
| rs767856521 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109043516 | GTTCTGGGAAAACTG[C/G]ATATCTATGTGCAAA | 84749 |
| rs767881802 | in-del | -/CACA | | | intron-variant | USP30 | GRCh38.p7 | 12:109081624 | ACGCACGCATGCGCG[-/CACA]CACACACACACACAC | 84749 |
| rs767886259 | snp | C/T | 3.29511e-05 | 0.00405887 | synonymous-codon | USP30 | GRCh38.p7 | 12:109085820 | CTCCGATGACACTGT[C/T]CGCAAGGCCAGCCTG | 84749 |
| rs767955791 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109024380 | CTCCCACCTCAGCCT[C/T]CCGAATAGCTGGGAT | 84749 |
| rs768043813 | snp | C/T | 1.64803e-05 | 0.00287052 | missense, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088390 | CTTTTCCCACGGGAA[C/T]CCTTATGCCGGAAGA | 84749 |
| rs768059846 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109077441 | TAAATTGTCCCTCTT[C/T]ATCTCTGCTAAGACT | 84749 |
| rs768070273 | snp | C/T | 1.64841e-05 | 0.00287085 | intron-variant | USP30 | GRCh38.p7 | 12:109081911 | TTTGAATTGTAGTAA[C/T]TTTCTTCTTCTCATG | 84749 |
| rs768121053 | snp | G/T | 1.65913e-05 | 0.00288017 | synonymous-codon, intron-variant | USP30 | GRCh38.p7 | 12:109057927 | TGCTTTTTTTTTAGG[G/T]CTTGTGCCTGGCCTT | 84749 |
| rs768124371 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109031260 | AAATGCTACTTTTGT[C/G]CATCATTTTTATGGA | 84749 |
| rs768278207 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109067044 | ATAGAGTACTAAGCA[C/T]TGGGTAAAGCTACAA | 84749 |
| rs768319786 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109062373 | GGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG | 84749 |
| rs768356251 | snp | G/T | 9.10871e-05 | 0.00674798 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052660 | GAGGAGACGGTTTCA[G/T]GCCTCCGGTGCGGCT | 84749 |
| rs768359915 | snp | C/G | 1.78979e-05 | 0.00299143 | intron-variant | USP30 | GRCh38.p7 | 12:109073401 | CTTGGTGCCAAAGGG[C/G]TAAAAGTGACATATC | 84749 |
| rs768373857 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109074494 | TTCATTCCCACCGGC[A/G]GTGTATGAGGGGTTC | 84749 |
| rs768430553 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109085588 | TCATCCCCTATTTAA[C/T]ATTAGCATTCTTTTG | 84749 |
| rs768446119 | snp | A/G | 1.65102e-05 | 0.00287312 | intron-variant | USP30 | GRCh38.p7 | 12:109072301 | TTTTTTTTCTCCCCT[A/G]CAGCAGCAGTCAGAA | 84749 |
| rs768482112 | in-del | -/TCCTTCATTTTTAAAGAAT | | | intron-variant | USP30 | GRCh38.p7 | 12:109036667 | GAATGTCTTAATTCC[-/TCCTTCATTTTTAAAGAAT]AGTTTTGCCAGATAT | 84749 |
| rs768544968 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109025947 | CCCACCTTGGCCAAA[G/T]GTGCTGGCATTACAG | 84749 |
| rs768606292 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109063959 | CTCACTGCGACCTCC[A/G]CCTCCTGAGTTCTAA | 84749 |
| rs768632689 | snp | A/T | 8.63342e-05 | 0.0065696 | splice-donor-variant, synonymous-codon | USP30 | GRCh38.p7 | 12:109083064 | AGCCCCCACACCAGG[A/T]GTGTGCGCGCGAGGA | 84749 |
| rs768650700 | snp | A/G | 1.6489e-05 | 0.00287128 | missense, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088429 | CTGCAGGCACCGAAG[A/G]AGACAGAGGCAATGG | 84749 |
| rs768673198 | snp | A/T | 1.64751e-05 | 0.00287007 | missense, intron-variant | USP30 | GRCh38.p7 | 12:109058027 | AGGTGGCTGGAAGAG[A/T]TCACCTCCCAGTACT | 84749 |
| rs768688743 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046591 | TATCTGGCCACTTTG[A/G]CCTAGCCAAAGTTGA | 84749 |
| rs768708065 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109040864 | TCACTCTCACAATAG[A/T]TTTTTCAATGTGAGA | 84749 |
| rs768755196 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054840 | TATTCTGTTGACTCT[A/G]TCTTGGAAAACAAAT | 84749 |
| rs768771556 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109047785 | TTGAGCCCAGGAGTT[C/T]GAGACCAGTCTGGGC | 84749 |
| rs768794684 | snp | A/C | 1.66615e-05 | 0.00288626 | intron-variant | USP30 | GRCh38.p7 | 12:109071596 | CCTCTCTAAAGAATG[A/C]TTTGCCCTATGACAG | 84749 |
| rs768800746 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109083949 | TGAGGTAGGGGACAG[A/G]CTCTGGTTCAGTCCT | 84749 |
| rs768959053 | snp | A/G | 2.05573e-05 | 0.00320597 | downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088171 | TCTTAGAGTCGAGAG[A/G]GAAAGAGAAAAGAGA | 84749 |
| rs768987249 | in-del | -/AT | 3.30011e-05 | 0.00406195 | intron-variant | USP30 | GRCh38.p7 | 12:109085648 | TTGTAAACCCCTGAC[-/AT]GTGTTCGTATCATTC | 84749 |
| rs769009100 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052854 | GCCCTAGTTGGGGTC[A/T]CCAGGGCCCGCGCGG | 84749 |
| rs769029359 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109082319 | CTTCCTTTTAACCTG[-/T]GCTACCTGCCTGACT | 84749 |
| rs769088061 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109084896 | GGTAATCAAAACCAG[C/G]TTTTGTTTACAGAGC | 84749 |
| rs769109644 | snp | C/T | | | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022063 | GGTCTTGCTTTGTTG[C/T]CCAGGCTGATCTAGA | 84749 |
| rs769114251 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109043126 | GAAACACATCCCAAG[C/T]CCATGGATTGGAAGA | 84749 |
| rs769148870 | snp | A/T | 1.67936e-05 | 0.00289767 | intron-variant | USP30 | GRCh38.p7 | 12:109082819 | GAAACAACTCGGTTC[A/T]CCCGATTTCTCTTCC | 84749 |
| rs769153327 | snp | G/T | 1.65488e-05 | 0.00287647 | missense, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088268 | GAGCCAGAACCTTCT[G/T]TCTCACGGGAAGACT | 84749 |
| rs769165386 | snp | C/T | 1.65499e-05 | 0.00287657 | missense | USP30 | GRCh38.p7 | 12:109082697 | TGAACGGGGAAAAGG[C/T]GGAACACCAGAGGAC | 84749 |
| rs769165668 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109057668 | TAGGAAGAACCAAGC[G/T]GTGCTGGATACCATG | 84749 |
| rs769205596 | snp | C/G | 2.77143e-05 | 0.00372241 | intron-variant, synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052750 | CTTCCTGCGGACCGG[C/G]GCGGCCGTCAGGTGA | 84749 |
| rs769206404 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109023121 | GCTGGGAAAGGGAGC[C/T]GGACAACCTGGTACC | 84749 |
| rs769223864 | snp | C/T | 1.65649e-05 | 0.00287788 | synonymous-codon | USP30 | GRCh38.p7 | 12:109073448 | TCCAGGGTCACCTCA[C/T]CCTACATCCAATCAC | 84749 |
| rs769261759 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055806 | AGACAGACAACAAAC[C/T]CAGTGCATTAAAAAA | 84749 |
| rs769275853 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109044530 | TAGTCCTAGCTACTC[A/G]CGAGGCTAGGGTGGA | 84749 |
| rs769361238 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109079922 | TTATTGTATGCTTAA[C/T]ATCATAATAGAGACA | 84749 |
| rs769419189 | snp | G/T | 1.65891e-05 | 0.00287998 | intron-variant | USP30 | GRCh38.p7 | 12:109056675 | GTAAACTTGTTTTCT[G/T]TTTTAGATATAAAGT | 84749 |
| rs769464967 | snp | A/G | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | USP30, USP30-AS1 | GRCh38.p7 | 12:109052433 | AGGCAACTGAGCCCA[A/G]CGTAGCAACCGACGC | 84749 |
| rs769465041 | snp | G/T | | | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109086637 | ATCTTTTGTATATTG[G/T]ACTGAGATGTAATTA | 84749 |
| rs769507185 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109065787 | CAGGAAGCAGTGGCC[A/C]TGCGCCAGAGAAGAA | 84749 |
| rs769515944 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109066811 | TTGGGAAACAGCCCT[G/T]TGGAGAGGAGTGTAG | 84749 |
| rs769560279 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109029870 | GGTGAGAGGGGCAAC[C/T]TTTGATTAACATTAA | 84749 |
| rs769652200 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109068537 | AAATGTATCTCAGTT[A/C]ATCCAATTGTATGTT | 84749 |
| rs769665424 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109024771 | ACTACAGGCGCCCAC[A/C]ACCACCCTGGGCTAA | 84749 |
| rs769673138 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109039750 | CAAATAGCTGGGACT[A/C]CAGGTGCCCGCCACC | 84749 |
| rs769680056 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109044559 | GAAGGATCATCTGAG[C/T]TCTGGAGTTCAAGGC | 84749 |
| rs769755370 | snp | A/G | 1.65184e-05 | 0.00287384 | intron-variant | USP30 | GRCh38.p7 | 12:109067483 | CTGGTTAGTTGTTAT[A/G]CTGATGAATTTAATA | 84749 |
| rs769758143 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109075681 | GGTAATAGCCATCCT[A/G]ACAGGTGTGCGGTGA | 84749 |
| rs769770015 | snp | C/T | 9.91522e-05 | 0.00704033 | missense | USP30 | GRCh38.p7 | 12:109072336 | CTCCCAAACAAATTA[C/T]CTGCCGCACAAGAGG | 84749 |
| rs769809734 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109050425 | TCAATCCTTTTTAAG[C/T]GTACAAAGAGATCCG | 84749 |
| rs769812759 | snp | C/T | | | downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088106 | ACATAACAAGCCCTA[C/T]GCTTTAAACCTTTCT | 84749 |
| rs769888794 | snp | A/G | | | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022471 | GGACTTGAAAATCCA[A/G]AATTGAATGTGTGCC | 84749 |
| rs769897444 | snp | A/T | 2.83354e-05 | 0.0037639 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052792 | GCGGGGCTGCCGAAG[A/T]GGCCGGGACCAGGGT | 84749 |
| rs769961519 | in-del | -/GCAC | | | intron-variant | USP30 | GRCh38.p7 | 12:109081623 | CACGCACGCATGCGC[-/GCAC]ACACACACACACACA | 84749 |
| rs769964227 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109074250 | GCATTACATGGATCT[A/G]CAACATTTTTATCCA | 84749 |
| rs769983536 | in-del | -/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109049035 | AGGTTTCTTGAAGGT[-/C]CCCTTGGCCAAGAGG | 84749 |
| rs770141071 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109083559 | GTAGCTATTATCGCC[A/G]GTCTTACTGATAAGA | 84749 |
| rs770142512 | snp | G/T | 4.94181e-05 | 0.00497057 | synonymous-codon | USP30 | GRCh38.p7 | 12:109085775 | TTCTGCCAGGAACCC[G/T]CTCTCAACTAGCAAT | 84749 |
| rs770150614 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046466 | TTAATTGGATGAGGC[A/C]CACCCACTATTTGGA | 84749 |
| rs770152519 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109062919 | ACTTTCTCTCTCTTT[A/G]AATTTGACTCAGACC | 84749 |
| rs770168746 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109032794 | TTGCACACTTTAAAG[A/G]CAGCTGCCTCCAGCC | 84749 |
| rs770187817 | snp | A/C | 1.675e-05 | 0.00289391 | intron-variant | USP30 | GRCh38.p7 | 12:109082828 | CGGTTCTCCCGATTT[A/C]TCTTCCACCCGCAGC | 84749 |
| rs770222569 | snp | C/T | 9.94233e-05 | 0.00704995 | intron-variant | USP30 | GRCh38.p7 | 12:109071609 | TGCTTTGCCCTATGA[C/T]AGGATGCTCACGAAT | 84749 |
| rs770288696 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109068300 | GGCCTTGTCCAGCTT[C/T]GTGTAGGCGTTGTCT | 84749 |
| rs770312535 | snp | A/G | 1.65081e-05 | 0.00287293 | intron-variant | USP30 | GRCh38.p7 | 12:109067659 | AACAGGTTTAGCTTG[A/G]AGAATCCTTTCCCCT | 84749 |
| rs770329605 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109041259 | CTGGGGAAAACAACC[C/G]ATAAATTAACAACAA | 84749 |
| rs770388527 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055645 | CAGGTGATCCGCCCA[C/T]CTCGGCCTCCCAAAG | 84749 |
| rs770395139 | snp | C/T | 1.6498e-05 | 0.00287206 | missense, intron-variant | USP30 | GRCh38.p7 | 12:109056711 | AGAACTGGGGAGTTA[C/T]AGGTGGAATTGCTGC | 84749 |
| rs770460813 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109057358 | CCTCCTTTTTTTGTG[C/T]CTTTGAGAACTTTGA | 84749 |
| rs770477426 | in-del | -/GACATG | 3.29457e-05 | 0.00405854 | cds-indel | USP30 | GRCh38.p7 | 12:109085730 | GACATGCACTCTGGA[-/GACATG]CACTTTGTCACTTAC | 84749 |
| rs770528768 | snp | C/T | 1.65012e-05 | 0.00287234 | stop-gained, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088290 | GGGAAGACTGTGGTA[C/T]CAGTGCGTGTTGGTC | 84749 |
| rs770601644 | snp | A/C | 4.94776e-05 | 0.00497357 | missense | USP30 | GRCh38.p7 | 12:109082912 | ACGCCTCTGAAGCGG[A/C]ATGAGCACGTGCAGT | 84749 |
| rs770618385 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109042647 | TTACAGAACATTATA[C/T]TCAATGGTGAGAGAC | 84749 |
| rs770646816 | snp | G/T | 1.72982e-05 | 0.00294088 | intron-variant | USP30 | GRCh38.p7 | 12:109057878 | CATGGGAGAGAAATT[G/T]ATCAAATGTGATATA | 84749 |
| rs770655413 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109028433 | GGAGCAAGACAGAGA[C/G]AGGGGAGGTGCCACA | 84749 |
| rs770666270 | snp | C/T | 1.65252e-05 | 0.00287443 | missense | USP30 | GRCh38.p7 | 12:109085037 | CAACGCTGTCAGCGC[C/T]GATGCCCTTCCCTCT | 84749 |
| rs770678819 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109079847 | TCCTTGAGCATATTT[A/G]TGATACATCTGTGAG | 84749 |
| rs770686420 | in-del | -/ATATA | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055395 | TATATATATATATAT[-/ATATA]ATATATTTTTTTTTT | 84749 |
| rs770704525 | in-del | -/ACAT | | | intron-variant | USP30 | GRCh38.p7 | 12:109085434 | ATAGTGTACATAAAC[-/ACAT]ACACTCATTGATACA | 84749 |
| rs770708835 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109027251 | CCTCCCTCCTCCCAG[C/T]CTCTGGTAACCTCTA | 84749 |
| rs770725122 | snp | C/T | 4.94466e-05 | 0.00497201 | synonymous-codon, missense, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088341 | GCTCCCGTGGGCCAG[C/T]GGCAGCCTGACCACC | 84749 |
| rs770806244 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109064543 | CCTCGGCCTCCCAGA[A/G]TGCTGGGATTACAGG | 84749 |
| rs770811444 | snp | A/G | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | USP30, USP30-AS1 | GRCh38.p7 | 12:109052278 | ATAACTAATTATAGC[A/G]GAGGCCTGACCCGAC | 84749 |
| rs770813615 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109036035 | CATGGTGGCCCATGG[A/C]TGTAGTCCCAGCTAA | 84749 |
| rs770838155 | in-del | -/T | 0.00182449 | 0.0301483 | intron-variant | USP30 | GRCh38.p7 | 12:109057915 | TCTTCTTCCCCCTGC[-/T]TTTTTTTTAGGGCTT | 84749 |
| rs770850030 | snp | A/G | 1.64947e-05 | 0.00287177 | intron-variant | USP30 | GRCh38.p7 | 12:109081287 | CATCTTTAAAACTTT[A/G]AACTAAGCCTAAATC | 84749 |
| rs770868437 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109051058 | TATTTTGTTTTTCTT[A/T]TCTTTGTTTTTCGGT | 84749 |
| rs770972942 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109037538 | ATAATATGGCAACTC[C/T]GGAAATCAGATTCTC | 84749 |
| rs771059909 | snp | A/G | | | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109086415 | TTGCTTTTGTAGCAC[A/G]TCCATTGTGAAATAT | 84749 |
| rs771064289 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109072564 | CTTTTCTTGAAACTG[A/G]CTTATTTGTACTTCA | 84749 |
| rs771128629 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109024682 | TGGAGTGCAGTGGCG[C/T]GATCTCAGCTCACTG | 84749 |
| rs771251473 | snp | C/T | 1.69349e-05 | 0.00290984 | missense | USP30 | GRCh38.p7 | 12:109083045 | AGCTGCAGGATGGGC[C/T]GGGAGCCCCCACACC | 84749 |
| rs771270733 | snp | A/G | 1.658e-05 | 0.00287919 | synonymous-codon | USP30 | GRCh38.p7 | 12:109082680 | TGAAGCCAAGGGAAC[A/G]TTGAACGGGGAAAAG | 84749 |
| rs771289025 | snp | A/G | 3.29462e-05 | 0.00405857 | missense | USP30 | GRCh38.p7 | 12:109082005 | CGGGATGTTGTGTGT[A/G]ACAACTGTACAAAGG | 84749 |
| rs771290346 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109032668 | GGAGGGGGAAATGGA[G/T]ATTGACTGCTAATAC | 84749 |
| rs771297494 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109074081 | TCTACCTCTGTCTCT[A/G]TGGATTTGCATATTC | 84749 |
| rs771310309 | in-del | -/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109059657 | TATCTGGGATTACAG[-/C]TGCATGCCACCACGC | 84749 |
| rs771313187 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046329 | CATGTTGGCCAGGAT[A/G]GTCTCGATCTCCTGA | 84749 |
| rs771319239 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109081075 | CATGGTTATTTCCTT[A/T]AAAATCCCAAAATTA | 84749 |
| rs771361539 | snp | C/T | 1.65348e-05 | 0.00287526 | synonymous-codon | USP30 | GRCh38.p7 | 12:109071692 | GGTCACACATTTGTT[C/T]GATGTGCATTCCCTG | 84749 |
| rs771362379 | snp | C/T | 1.65233e-05 | 0.00287426 | synonymous-codon | USP30 | GRCh38.p7 | 12:109071620 | ATGACAGGATGCTCA[C/T]GAATTATTCCATGTC | 84749 |
| rs771386393 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109082448 | CAGAGCATCAGTGTT[C/T]GCTCTTCACATTCTC | 84749 |
| rs771458699 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109060461 | ATCTTTATGAAGCAA[C/G]TGTACTTTTCTGTGG | 84749 |
| rs771516419 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109062841 | CATCCCGTACTGAAA[C/T]TGTACCCATGAAACA | 84749 |
| rs771525400 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109068413 | TTTGGAAAGGGAGCT[A/G]GGGAGGCTTTCTAGC | 84749 |
| rs771697813 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054111 | TGATTAGGGGATTTT[A/G]AAGCACTGGTAAAGC | 84749 |
| rs771730230 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109035884 | AAAAAATACATGGGC[C/T]AGGCACAATGACTTA | 84749 |
| rs771756995 | in-del | -/TTGTT | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109047439 | TTGAGACATTTATTA[-/TTGTT]TTGTTTTGGCCCCCA | 84749 |
| rs771766920 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055256 | TCAGCTCTTTTATAC[A/C]ATTGTATGTGTGCCC | 84749 |
| rs771808325 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109041141 | ATTAGAAAGAAAACA[A/G]TTGTTTCCTTAAGAT | 84749 |
| rs771837000 | snp | A/G | 1.84211e-05 | 0.00303483 | intron-variant, missense | USP30 | GRCh38.p7 | 12:109083089 | CGAGGAGCCGATGCA[A/G]CAGGAATTTTCAGCA | 84749 |
| rs771842370 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109028464 | CCTTTTTTTTTTCTG[-/T]TTTTTTTGTTGTTGT | 84749 |
| rs771853893 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109063179 | ATCTTAGCTCACTGC[A/C]ACTTCCGCCTTCCAG | 84749 |
| rs771855503 | snp | C/T | 1.706e-05 | 0.00292057 | missense | USP30 | GRCh38.p7 | 12:109083057 | GGCCGGGAGCCCCCA[C/T]ACCAGGTGTGTGCGC | 84749 |
| rs771863488 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109040055 | CTTATTTTCACATAT[A/G]TTAGAAAAATATTGT | 84749 |
| rs771906756 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109076196 | TGGAATTTAAAAAAA[C/T]TTATTTTCAAATTGT | 84749 |
| rs771931523 | snp | C/G | 3.43525e-05 | 0.00414428 | intron-variant | USP30 | GRCh38.p7 | 12:109057896 | CAAATGTGATATACT[C/G]TTCTCTTCTTCCCCC | 84749 |
| rs771932729 | in-del | -/CTTGCA | 1.69006e-05 | 0.00290689 | intron-variant | USP30 | GRCh38.p7 | 12:109084945 | CTCGGGCCTTTTTCT[-/CTTGCA]CTTGCAGTTCTGAAT | 84749 |
| rs772007979 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109049475 | ATTACAATAGTAACA[A/T]TAAGGATCACTGATC | 84749 |
| rs772021336 | snp | C/T | 1.64931e-05 | 0.00287163 | missense, intron-variant | USP30 | GRCh38.p7 | 12:109056735 | TTGCTGCTGCTCTTG[C/T]AGCAGGAATATATGT | 84749 |
| rs772069434 | snp | A/C | 1.64814e-05 | 0.00287061 | intron-variant | USP30 | GRCh38.p7 | 12:109081421 | TTATGGTTTATTTGG[A/C]GTCTGTTTCAGAAAC | 84749 |
| rs772106516 | snp | C/G | 1.64817e-05 | 0.00287064 | missense, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088352 | CCAGCGGCAGCCTGA[C/G]CACCGCCACCCTCCT | 84749 |
| rs772169843 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109034359 | ATTTCAATTCTTTTA[A/C]ATTTTGAGGCTTATT | 84749 |
| rs772200863 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109028216 | TTTAATTGAATTGTT[C/T]GGGGATTTTTGCTGT | 84749 |
| rs772232376 | in-del | -/TATGACA | 1.66032e-05 | 0.0028812 | intron-variant | USP30 | GRCh38.p7 | 12:109071603 | AAGAATGCTTTGCCC[-/TATGACA]TATGACAGGATGCTC | 84749 |
| rs772352184 | snp | C/T | 1.64863e-05 | 0.00287104 | intron-variant | USP30 | GRCh38.p7 | 12:109067640 | CAGGTGAGTACAACA[C/T]TTGAACAGGTTTAGC | 84749 |
| rs772367199 | snp | A/G | 1.64808e-05 | 0.00287057 | missense, intron-variant | USP30 | GRCh38.p7 | 12:109057967 | GGGAACACCTGCTTC[A/G]TGAACTCCCTGCTAC | 84749 |
| rs772442591 | snp | A/G | 1.64811e-05 | 0.00287059 | intron-variant | USP30 | GRCh38.p7 | 12:109082046 | ACCCCAAATGTCATC[A/G]CCAGCTGGCCTGTGT | 84749 |
| rs772469471 | snp | A/G | | | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109086169 | GCATTCATTATGTCC[A/G]GAGTGTCTTTTTACT | 84749 |
| rs772475501 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109058942 | GTAACTTAGTGCCAC[C/T]TTTCTGGAAAGCAGT | 84749 |
| rs772489006 | snp | A/G | 0.000103557 | 0.00719499 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052653 | GGTAGCGGAGGAGAC[A/G]GTTTCAGGCCTCCGG | 84749 |
| rs772529029 | snp | C/G/T | 1.69301e-05 | 0.00290942 | intron-variant | USP30 | GRCh38.p7 | 12:109072402 | TGGACTTTTAAGATA[C/G/T]GATAATAATTTGCTT | 84749 |
| rs772572510 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109044745 | AATGCTGTAATAAAT[A/G]TGTTTATTCTTCTAC | 84749 |
| rs772665984 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109080182 | TAAACTTTGGGGCTC[A/T]TCCCCTCTGTGTCTC | 84749 |
| rs772700774 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109029679 | TGCTTACTGTTAGAA[A/G]AGAAGTGATTTCCTT | 84749 |
| rs772717099 | snp | G/T | 2.75228e-05 | 0.00370953 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052769 | GCCGTCAGGTGAGAT[G/T]TTGGGGGGCGGGGCT | 84749 |
| rs772729977 | snp | A/C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109077076 | CCTTTCTGGGATAAA[A/C/T]CCCACTTGATCATGA | 84749 |
| rs772761909 | snp | A/G | 1.66888e-05 | 0.00288862 | missense, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088237 | AAAATTTTACGAAAA[A/G]TCAGATTCACCCGTG | 84749 |
| rs772775278 | snp | C/T | 6.60327e-05 | 0.00574561 | missense, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088283 | TTCTCACGGGAAGAC[C/T]GTGGTACCAGTGCGT | 84749 |
| rs772780348 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054162 | GTCCTTTATAATCTT[C/T]CCAGGCACTTTTGTG | 84749 |
| rs772798071 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109040057 | TATTTTCACATATAT[C/T]AGAAAAATATTGTTT | 84749 |
| rs772943440 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109047920 | GCAGGCTCCCTAAGG[A/G]TGCTCAAGACCCTTT | 84749 |
| rs772945304 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109064382 | TGATCCTCCTGCCAC[A/G]GCTTCCCAAGTATTT | 84749 |
| rs772995162 | snp | A/G | 7.82197e-05 | 0.0062533 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052667 | CGGTTTCAGGCCTCC[A/G]GTGCGGCTGCAATGC | 84749 |
| rs772998474 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109063224 | CCTGCCTCAGCCTTC[C/T]GAGTAGCTGGGATGA | 84749 |
| rs773069263 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109077832 | GTTTGTGTTGGGGGG[G/T]GAGGGTGTGTGTGAG | 84749 |
| rs773104683 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109049543 | TTTGGGACCAGGCAC[A/G]GTGGCTCACGCCTGT | 84749 |
| rs773108011 | snp | A/T | | | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022242 | AGAAAAGCTGGAAAA[A/T]TATACAACAGAAAAC | 84749 |
| rs773141350 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109062925 | TCTCTCTTTGAATTT[G/T]ACTCAGACCTCATTA | 84749 |
| rs773144773 | in-del | -/TAGAAACTTGTAAGGTT | | | intron-variant | USP30 | GRCh38.p7 | 12:109072214 | GTGGTGTAATCAACG[-/TAGAAACTTGTAAGGTT]TAGGGGTGGGGTGAG | 84749 |
| rs773197378 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109027198 | GATCTTGATCATCCC[A/G]AAGAGAAACTCTACC | 84749 |
| rs773215502 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109084121 | CAATCCCAGCACTTT[A/G]GGAGATTGAGGTGGG | 84749 |
| rs773303115 | in-del | -/TT/TTT | | | intron-variant | USP30 | GRCh38.p7 | 12:109062328 | CTCTACCTCCTTCAC[-/TT/TTT]TTTTTTTTTTTTTTT | 84749 |
| rs773305476 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109071446 | TGAGGGTCTTCACTC[A/G]TGACAGTGTCCAGGA | 84749 |
| rs773361416 | snp | G/T | 3.29614e-05 | 0.00405951 | intron-variant | USP30 | GRCh38.p7 | 12:109081318 | GTTTCTGGATTTTCT[G/T]CAATATTTCTTTCAG | 84749 |
| rs773400469 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109024565 | GCCCGGCCACAATGA[A/T]TAATTTTAAGTATCA | 84749 |
| rs773455265 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon | USP30 | GRCh38.p7 | 12:109085679 | CAGCTCCTCCACATA[C/T]CTCTTCCGGCTGATG | 84749 |
| rs773456346 | snp | C/T | 1.70168e-05 | 0.00291687 | intron-variant | USP30 | GRCh38.p7 | 12:109057916 | CTTCTTCCCCCTGCT[C/T]TTTTTTTAGGGCTTG | 84749 |
| rs773464619 | snp | A/G | 3.2956e-05 | 0.00405918 | missense, intron-variant | USP30 | GRCh38.p7 | 12:109058045 | ACCTCCCAGTACTCC[A/G]GGGATCAGAAGGAGC | 84749 |
| rs773484410 | snp | C/T | 1.67343e-05 | 0.00289255 | intron-variant | USP30 | GRCh38.p7 | 12:109082833 | CTCCCGATTTCTCTT[C/T]CACCCGCAGCTCCCT | 84749 |
| rs773495177 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046970 | CCAAAGTGGTGGGAT[C/T]ACAGGGGTTGAGCCA | 84749 |
| rs773510096 | snp | A/T | 1.65097e-05 | 0.00287308 | intron-variant | USP30 | GRCh38.p7 | 12:109067663 | GGTTTAGCTTGGAGA[A/T]TCCTTTCCCCTAGTG | 84749 |
| rs773515537 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109023426 | CAGGTGTGGTGGCAC[A/C]GACCTGTAGTCCCAG | 84749 |
| rs773519160 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109058961 | CTGGAAAGCAGTTTG[C/G]AACTACACAATAATA | 84749 |
| rs773545327 | in-del | -/TT | | | intron-variant | USP30 | GRCh38.p7 | 12:109056197 | TTGTTGTTGTTGTTG[-/TT]GTTGTTTTTTATGAG | 84749 |
| rs773551086 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109072471 | CTTGAAGTGTGATGT[C/G]CTTGCAAAGGAACTT | 84749 |
| rs773604522 | in-del | -/TG | | | intron-variant | USP30 | GRCh38.p7 | 12:109077812 | TTTTAGCTTTACTCT[-/TG]TGTGTTTGTGTTGGG | 84749 |
| rs773607081 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109029726 | GAAAGGGACCTGGAA[C/T]AAAGTGGCAGTGTTT | 84749 |
| rs773632815 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109043530 | GGATATCTATGTGCA[A/G]AAGAATGAAGTTGCC | 84749 |
| rs773664772 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109026651 | TTTTGTATTTTTTCT[A/G]GGGAAGGAGTCTCAC | 84749 |
| rs773739110 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109030251 | CAGATTATTTTCCCT[C/G]TTTGAGTCTCAGTTG | 84749 |
| rs773763399 | snp | A/G | 1.65529e-05 | 0.00287683 | missense | USP30 | GRCh38.p7 | 12:109071612 | TTTGCCCTATGACAG[A/G]ATGCTCACGAATTAT | 84749 |
| rs773795397 | in-del | -/TT | 1.6473e-05 | 0.00286988 | frameshift-variant | USP30 | GRCh38.p7 | 12:109085734 | ATGCACTCTGGACAC[-/TT]TGTCACTTACCGACG | 84749 |
| rs773805067 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109062616 | TACAGGCTTGAGCCA[C/T]CGCGCCCAGCCTTTT | 84749 |
| rs773843423 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109066013 | TCCCAGCACGTTGGG[A/C]GGCCAAGGTGGGCAG | 84749 |
| rs773885684 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109059525 | ATTTTTATTTTATTT[C/T]ATTTTTGAGACAGAG | 84749 |
| rs773904047 | snp | A/G | 8.34578e-05 | 0.00645925 | intron-variant | USP30 | GRCh38.p7 | 12:109082839 | ATTTCTCTTCCACCC[A/G]CAGCTCCCTCAGTGT | 84749 |
| rs773908570 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109031309 | TACACATGTGTCCTC[A/C]ATGGCATTGTCTTTG | 84749 |
| rs773921791 | snp | G/T | 1.64912e-05 | 0.00287147 | missense | USP30 | GRCh38.p7 | 12:109082914 | GCCTCTGAAGCGGCA[G/T]GAGCACGTGCAGTTC | 84749 |
| rs773960762 | snp | C/T | 1.65184e-05 | 0.00287384 | intron-variant | USP30 | GRCh38.p7 | 12:109085643 | TAAAATTGTAAACCC[C/T]TGACATGTGTTCGTA | 84749 |
| rs773988604 | snp | A/G | 1.64825e-05 | 0.00287071 | missense, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088342 | CTCCCGTGGGCCAGC[A/G]GCAGCCTGACCACCG | 84749 |
| rs774006489 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109067202 | CACTGCAAGCTCCGC[C/G]TCCCGGGTTCATGCC | 84749 |
| rs774007470 | in-del | -/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109084420 | AATGCTTAGATCAGT[-/G]GTTCTCAACTTGGAG | 84749 |
| rs774065152 | snp | A/C | 1.64944e-05 | 0.00287175 | missense | USP30 | GRCh38.p7 | 12:109073477 | ACTGGAAGTCTCAAC[A/C]TCCTTTTCATGGAAG | 84749 |
| rs774095865 | in-del | -/AATA | | | intron-variant | USP30 | GRCh38.p7 | 12:109023558 | AACTCTGTCTCAATA[-/AATA]AATAAATAAATAAAT | 84749 |
| rs774119148 | snp | C/T | | | intron-variant, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053698 | GACCTCATAGCAGAG[C/T]TGGGAGGAGAAGCCA | 84749 |
| rs774129865 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109025950 | ACCTTGGCCAAAGGT[G/T]CTGGCATTACAGGTG | 84749 |
| rs774147033 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109074650 | TTATTGAGATCTAAT[A/C]GACAATAAAAATTGT | 84749 |
| rs774192141 | in-del | -/TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT | | | intron-variant | USP30 | GRCh38.p7 | 12:109079358 | TTTTTTTCTTTTTTT[lengthTooLong]TTTTTTTTTTTTTTT | 84749 |
| rs774239235 | snp | G/T | 1.64958e-05 | 0.00287187 | stop-gained, intron-variant | USP30 | GRCh38.p7 | 12:109056716 | TGGGGAGTTATAGGT[G/T]GAATTGCTGCTGCTC | 84749 |
| rs774328555 | snp | C/T | 1.66549e-05 | 0.00288568 | missense | USP30 | GRCh38.p7 | 12:109085878 | CTGCTGTTCTACGAG[C/T]GCGTCCTTTCCAGGA | 84749 |
| rs774328936 | snp | C/G | 1.64893e-05 | 0.0028713 | intron-variant | USP30 | GRCh38.p7 | 12:109081294 | AAAACTTTGAACTAA[C/G]CCTAAATCGTTTCTG | 84749 |
| rs774329273 | snp | C/T | 1.73531e-05 | 0.00294555 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052787 | GGGGGGCGGGGCTGC[C/T]GAAGAGGCCGGGACC | 84749 |
| rs774365430 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109047801 | GAGACCAGTCTGGGC[A/G]ACATGGTGAAACCCT | 84749 |
| rs774503821 | snp | A/T | 0.000199415 | 0.00998337 | intron-variant | USP30 | GRCh38.p7 | 12:109057922 | CCCCCTGCTTTTTTT[A/T]TAGGGCTTGTGCCTG | 84749 |
| rs774518144 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109032928 | AAAACAAAAGTGAAT[A/C]CTTTAAGGGAGACTG | 84749 |
| rs774583287 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109071403 | CACCTGGCTTTCTCT[C/T]CTGCTCTCTGCTCCT | 84749 |
| rs774590814 | in-del | -/AATA | | | intron-variant | USP30 | GRCh38.p7 | 12:109023555 | GCGAAACTCTGTCTC[-/AATA]AATAAATAAATAAAT | 84749 |
| rs774591766 | snp | C/T | 1.64866e-05 | 0.00287106 | intron-variant | USP30 | GRCh38.p7 | 12:109081902 | TAGCTGTCCTTTGAA[C/T]TGTAGTAATTTTCTT | 84749 |
| rs774600494 | snp | C/T | 3.32005e-05 | 0.00407421 | missense, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088471 | GCCAGTTCTCTTTCA[C/T]CATCTCGGTGCTCCC | 84749 |
| rs774664424 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109084036 | GGGGTGCAGGTTTAC[C/T]AATGTTGAGAGCATG | 84749 |
| rs774717591 | snp | A/G | 1.65408e-05 | 0.00287578 | missense | USP30 | GRCh38.p7 | 12:109071694 | TCACACATTTGTTTG[A/G]TGTGCATTCCCTGGA | 84749 |
| rs774847973 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109023925 | GGTGTGATCACCACC[A/G]CGACTGGCCAATCAG | 84749 |
| rs774904327 | snp | A/G | | | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022153 | TGAGCCATTGCGCCC[A/G]GCCTCAGGGTATTTT | 84749 |
| rs775072013 | snp | A/G | 1.64923e-05 | 0.00287156 | missense | USP30 | GRCh38.p7 | 12:109071633 | CACGAATTATTCCAT[A/G]TCATTACCTCGTCAT | 84749 |
| rs775082372 | snp | A/G | 1.70816e-05 | 0.00292242 | synonymous-codon | USP30 | GRCh38.p7 | 12:109083058 | GCCGGGAGCCCCCAC[A/G]CCAGGTGTGTGCGCG | 84749 |
| rs775091967 | snp | A/T | 1.64825e-05 | 0.00287071 | intron-variant | USP30 | GRCh38.p7 | 12:109081429 | TATTTGGAGTCTGTT[A/T]CAGAAACATTTCAAT | 84749 |
| rs775098669 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109065851 | TTTTCCCTTGGCATA[A/G]TGCATTTAGAAGGTC | 84749 |
| rs775153676 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109079991 | ATTAATTTTCTTCTG[A/G]CCTGCAGTTAACCTG | 84749 |
| rs775161916 | snp | A/G | 4.94711e-05 | 0.00497324 | missense | USP30 | GRCh38.p7 | 12:109082921 | AAGCGGCATGAGCAC[A/G]TGCAGTTCAATGAGT | 84749 |
| rs775209475 | snp | A/G | 1.64936e-05 | 0.00287168 | missense, intron-variant | USP30 | GRCh38.p7 | 12:109056740 | GCTGCTCTTGCAGCA[A/G]GAATATATGTTATTT | 84749 |
| rs775212404 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109036236 | GCTCTTTATTTCCCC[A/G]TGTGGGTTTGAATTA | 84749 |
| rs775276257 | in-del | -/GC | | | intron-variant | USP30 | GRCh38.p7 | 12:109081622 | CACGCACGCATGCGC[-/GC]GCACACACACACACA | 84749 |
| rs775276325 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109074435 | TCTTTTGTTTAACCT[C/T]TTAAGGAACTGCCAG | 84749 |
| rs775314504 | snp | A/C | | | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109086797 | TTATTGCCCATGCAG[A/C]GCTCTTAAGGTTTAC | 84749 |
| rs775335167 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109036746 | TAATACTTTGAATAT[A/G]TCCTTCTACTACCTT | 84749 |
| rs775339585 | snp | C/T | 1.64819e-05 | 0.00287066 | synonymous-codon, stop-gained, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088353 | CAGCGGCAGCCTGAC[C/T]ACCGCCACCCTCCTG | 84749 |
| rs775340201 | snp | A/G | 1.83474e-05 | 0.00302876 | intron-variant | USP30 | GRCh38.p7 | 12:109071740 | TTTCCAACACGTTCT[A/G]TGCAGCTTGTGCATA | 84749 |
| rs775372683 | snp | C/G | 1.64977e-05 | 0.00287203 | intron-variant | USP30 | GRCh38.p7 | 12:109067502 | ATGAATTTAATAATT[C/G]TCTTACCTTTTTTGT | 84749 |
| rs775388148 | snp | C/T | 3.29674e-05 | 0.00405988 | intron-variant | USP30 | GRCh38.p7 | 12:109081306 | TAAGCCTAAATCGTT[C/T]CTGGATTTTCTGCAA | 84749 |
| rs775438762 | snp | C/T | | | downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088108 | ATAACAAGCCCTACG[C/T]TTTAAACCTTTCTGT | 84749 |
| rs775455415 | in-del | -/A | 0.000102616 | 0.00716221 | downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088173 | TTAGAGTCGAGAGGG[-/A]AAGAGAAAAGAGAAA | 84749 |
| rs775473758 | snp | G/T | 3.43643e-05 | 0.00414499 | intron-variant | USP30 | GRCh38.p7 | 12:109057897 | AAATGTGATATACTG[G/T]TCTCTTCTTCCCCCT | 84749 |
| rs775537340 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109072863 | AAAGTTGATGATACT[G/T]GAGTTAATGGGATAA | 84749 |
| rs775625117 | snp | C/T | | | missense | USP30 | GRCh38.p7 | 12:109082664 | TCCTTTTATTTCAGA[C/T]TGAAGCCAAGGGAAC | 84749 |
| rs775659234 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046488 | CTATTTGGAGGGCAA[C/G]CTATTTTACTCAAAA | 84749 |
| rs775670436 | snp | C/G | 1.651e-05 | 0.0028731 | missense, intron-variant | USP30 | GRCh38.p7 | 12:109058071 | GGAGCCCCCCTCACA[C/G]CAGTATTTATCCTTA | 84749 |
| rs775741393 | snp | A/G | 1.70069e-05 | 0.00291602 | intron-variant | USP30 | GRCh38.p7 | 12:109084935 | ATTTTCATTGACTCG[A/G]GCCTTTTTCTCTTGC | 84749 |
| rs775777345 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109083738 | TCACTTGAAGGGCTC[A/G]CAGCCTGAACTCACC | 84749 |
| rs775790531 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109070201 | CTGCAGTTATCTGGC[C/T]GAGATGGTGTGGCTC | 84749 |
| rs775803273 | in-del | -/TCGTCA | 1.6486e-05 | 0.00287102 | cds-indel | USP30 | GRCh38.p7 | 12:109071642 | TTCCATGTCATTACC[-/TCGTCA]TTGGAAGATGAGCGA | 84749 |
| rs775820613 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109031687 | AAATGAATGACGTTC[A/C]AATAGAAGCTACAAT | 84749 |
| rs775821199 | snp | A/G | 1.68718e-05 | 0.00290441 | missense | USP30 | GRCh38.p7 | 12:109085890 | GAGCGCGTCCTTTCC[A/G]GGATGCAGCACCAGA | 84749 |
| rs775826768 | snp | A/G | | | utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109047706 | AGTGACTTACTCAGA[A/G]TGTGTTGGGTAAGTG | 84749 |
| rs775840191 | in-del | -/TTTT | | | intron-variant | USP30 | GRCh38.p7 | 12:109036308 | GTATTTCTTTCTTTC[-/TTTT]TTTTTTTTTTAGGGA | 84749 |
| rs775843447 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109068754 | GAAGTATTTCCAACA[C/T]CTTCAGCCCACAGCA | 84749 |
| rs775876815 | snp | C/T | 9.66978e-05 | 0.00695266 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052658 | CGGAGGAGACGGTTT[C/T]AGGCCTCCGGTGCGG | 84749 |
| rs775901924 | in-del | -/A | | | intron-variant | USP30 | GRCh38.p7 | 12:109066667 | TCCACCCTGGGCGAC[-/A]GAGCACGACTCTGTT | 84749 |
| rs775942841 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109042722 | CTTTCACAACTTCTA[C/T]TTAACGTAGTACTGG | 84749 |
| rs776042430 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055679 | TGGGATTACAGGCAT[A/G]AGCCATCACACCTGG | 84749 |
| rs776059668 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109032802 | TTTAAAGGCAGCTGC[C/T]TCCAGCCCACCACAT | 84749 |
| rs776070618 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109039153 | TGCTTTTTGTGATCT[A/G]TCTATGAAATCTTTG | 84749 |
| rs776112137 | snp | A/C | 6.59239e-05 | 0.00574087 | intron-variant | USP30 | GRCh38.p7 | 12:109082048 | CCCAAATGTCATCGC[A/C]AGCTGGCCTGTGTGT | 84749 |
| rs776152619 | snp | A/G | 1.6513e-05 | 0.00287336 | synonymous-codon | USP30 | GRCh38.p7 | 12:109072316 | ACAGCAGCAGTCAGA[A/G]ATAACTCCCAAACAA | 84749 |
| rs776243810 | snp | A/T | 1.6476e-05 | 0.00287014 | missense, intron-variant | USP30 | GRCh38.p7 | 12:109058040 | AGTTCACCTCCCAGT[A/T]CTCCAGGGATCAGAA | 84749 |
| rs776276525 | snp | A/G | 1.65021e-05 | 0.00287241 | missense, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088444 | GAGACAGAGGCAATG[A/G]GGCTCCCAGGGGCCA | 84749 |
| rs776313842 | snp | A/G | 1.98257e-05 | 0.00314841 | intron-variant | USP30 | GRCh38.p7 | 12:109071760 | GCTTGTGCATATTTA[A/G]TAAGTATAGGGGAGG | 84749 |
| rs776314602 | snp | A/G | 1.73096e-05 | 0.00294185 | missense | USP30 | GRCh38.p7 | 12:109085905 | AGGATGCAGCACCAG[A/G]GCCAGGAGTGCAAGT | 84749 |
| rs776340489 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109085445 | AAACACATACACTCA[C/T]TGATACAAACATCCA | 84749 |
| rs776357162 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109066294 | TGTTTATTTTCTGGA[C/G]TTTTACAGAAAAAGT | 84749 |
| rs776404631 | snp | A/G | 5.54677e-05 | 0.005266 | intron-variant, missense, utr-variant-5-prime, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052751 | TTCCTGCGGACCGGG[A/G]CGGCCGTCAGGTGAG | 84749 |
| rs776425386 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053216 | TCCTATAAGTGCCCC[A/G]GGCCTGCGAGCCCCG | 84749 |
| rs776489435 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109065677 | CTGTTGTAAAGAGGT[A/G]ATAATCACAAGGATC | 84749 |
| rs776496453 | snp | C/T | 0.000614925 | 0.0175238 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052662 | GGAGACGGTTTCAGG[C/T]CTCCGGTGCGGCTGC | 84749 |
| rs776515777 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109036104 | GGTTGAGGCTGAAGT[A/G]AGTCAGGGTTTCACC | 84749 |
| rs776538166 | in-del | -/A | | | intron-variant | USP30 | GRCh38.p7 | 12:109041970 | TTATTTTTTAATTAT[-/A]AAAAAAATTGTAGAA | 84749 |
| rs776538225 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109025680 | AAGTGGAACTGCCAC[-/T]TTTTTTTTTTTGACA | 84749 |
| rs776552800 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109047185 | TTTTTTTTTTTTAAC[C/T]GAGGAAACCCTTCTT | 84749 |
| rs776634874 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109024035 | GTTAAAGCAGGCTCA[C/G]TCCTGGGGACTCTCT | 84749 |
| rs776657741 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109085137 | CTTCTAAAATTAGCT[C/T]TTCACAGAAATGAAT | 84749 |
| rs776702446 | snp | C/T | 3.55777e-05 | 0.00421753 | intron-variant | USP30 | GRCh38.p7 | 12:109071732 | CATTAATATTTCCAA[C/T]ACGTTCTGTGCAGCT | 84749 |
| rs776709468 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109024683 | GGAGTGCAGTGGCGC[A/G]ATCTCAGCTCACTGC | 84749 |
| rs776744804 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109037552 | CTGGAAATCAGATTC[C/T]CCTCCCTCCTCAGGG | 84749 |
| rs776809144 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109059005 | TCAGTACTGTTTGAC[C/G]CAGTAATTCCATGTC | 84749 |
| rs776860484 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109072644 | ATGAGCTGAATCTGT[C/T]GTGTCCTCAGCATTT | 84749 |
| rs776862697 | in-del | -/A | | | intron-variant | USP30 | GRCh38.p7 | 12:109076205 | AAAAAATTTATTTTC[-/A]AATTGTTTGCCACTA | 84749 |
| rs776873115 | in-del | -/A | | | intron-variant | USP30 | GRCh38.p7 | 12:109067801 | GATCAGAGGGGAGAT[-/A]ACAGCTGTTTTTCAC | 84749 |
| rs776920053 | in-del | -/GTC | 0.000214131 | 0.010345 | cds-indel | USP30 | GRCh38.p7 | 12:109085701 | CGGCTGATGGCAGTT[-/GTC]GTCCACCATGGAGAC | 84749 |
| rs776925711 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046348 | TCGATCTCCTGACCT[C/T]GTGATCTGCCCACCT | 84749 |
| rs776952861 | snp | A/G | 1.64819e-05 | 0.00287066 | intron-variant | USP30 | GRCh38.p7 | 12:109085656 | CCCTGACATGTGTTC[A/G]TATCATTCAGCTCCT | 84749 |
| rs776967033 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109060559 | AAAAATGTGCAACTC[A/G]CTGCCAGCGTTCATC | 84749 |
| rs777010859 | snp | A/G | 5.74124e-05 | 0.00535751 | downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088184 | AGGGAAAGAGAAAAG[A/G]GAAAAACTGTTAAAA | 84749 |
| rs777087023 | snp | A/G | 3.41472e-05 | 0.00413188 | intron-variant | USP30 | GRCh38.p7 | 12:109073566 | CTTGATATTTCCGGG[A/G]GAGGTTTTCCAAAAG | 84749 |
| rs777153673 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109076290 | AACATTCATTTATTA[C/T]TTCTAGAAGCTGTAG | 84749 |
| rs777192957 | in-del | -/AATATACAGATAT | 1.66335e-05 | 0.00288383 | intron-variant | USP30 | GRCh38.p7 | 12:109056794 | AGCGTAGAAAAGGTA[-/AATATACAGATAT]AGAATGAGAACACTG | 84749 |
| rs777193221 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109033968 | AAAGGACAAACTCCA[A/C]AAGTCTCCTAGTAAA | 84749 |
| rs777253536 | snp | G/T | 1.64808e-05 | 0.00287057 | intron-variant | USP30 | GRCh38.p7 | 12:109067516 | TGTCTTACCTTTTTT[G/T]TTTCCAGCCTTGTCC | 84749 |
| rs777264265 | snp | A/G | | | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109021772 | CAGTTCAGGCTGCAT[A/G]TAAGAATTGCCTGGC | 84749 |
| rs777286079 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109071226 | GTACAACAACATGAA[C/T]GTACTTAATGCCACA | 84749 |
| rs777307269 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109075843 | CATGTTACTTTTTCT[-/T]TTTTTTTTTTTTTTT | 84749 |
| rs777319665 | in-del | -/GGTC | 1.64784e-05 | 0.00287035 | splice-acceptor-variant | USP30 | GRCh38.p7 | 12:109081932 | CTTCTCATGCTGTAG[-/GGTC]GGTCACCCATTGACC | 84749 |
| rs777333858 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109084645 | GGTTTAGGTCAAAAG[C/T]CAGTAAATTAGCTAC | 84749 |
| rs777353054 | snp | C/T | 1.65488e-05 | 0.00287647 | utr-variant-5-prime, synonymous-codon, intron-variant | USP30 | GRCh38.p7 | 12:109056685 | TTTCTTTTTTAGATA[C/T]AAAGTCATGAAGAAC | 84749 |
| rs777387521 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109079454 | CTGCAGCCTCAACCT[C/T]CCAGGCTCAAGTTAT | 84749 |
| rs777391421 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109049296 | TCCCTCGAACATTTA[C/G]AGGCGTGGACTGAAA | 84749 |
| rs777446724 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109057167 | TGGTAAAAATTTCAA[C/G]TTAGTGCCTTCATTA | 84749 |
| rs777641185 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109044070 | TATGCCACACCATAA[A/G]TGAACCTTGAGGACA | 84749 |
| rs777661868 | snp | C/T | 1.64825e-05 | 0.00287071 | intron-variant | USP30 | GRCh38.p7 | 12:109067635 | AAGAACAGGTGAGTA[C/T]AACATTTGAACAGGT | 84749 |
| rs777741059 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109080341 | CAAACACACAAATCT[C/T]GCCCACAGAGTTCTG | 84749 |
| rs777778730 | snp | G/T | 1.65075e-05 | 0.00287289 | intron-variant | USP30 | GRCh38.p7 | 12:109072286 | TTTTCAGTCTGTTTT[G/T]TTTTTTTCTCCCCTA | 84749 |
| rs777887239 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109037251 | ACTTTTCAACTTCAG[A/G]ATTTCTACTTCATTC | 84749 |
| rs777894010 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109050914 | CAGGAGGCTGAGGCA[A/G]GATAATCGCTTGAAC | 84749 |
| rs777966158 | snp | A/T | | | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109086189 | GTCTTTTTACTCATC[A/T]GATACAGGTAATTAA | 84749 |
| rs778109255 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109062731 | CAAAATATCCATAAC[A/G]TAAAATTTACCATTT | 84749 |
| rs778114585 | snp | A/G | 9.88321e-05 | 0.00702896 | missense | USP30 | GRCh38.p7 | 12:109081991 | CATCAGAATCAGTGC[A/G]GGATGTTGTGTGTGA | 84749 |
| rs778148608 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109060376 | AAGGAGAAAATTGGA[C/T]TTAAAAAACATTCAG | 84749 |
| rs778197910 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109025563 | TGGAAATCAACAGAA[C/G]ATGTCCAAAATTGAG | 84749 |
| rs778204248 | snp | C/T | 1.66192e-05 | 0.00288259 | synonymous-codon | USP30 | GRCh38.p7 | 12:109085874 | CTACCTGCTGTTCTA[C/T]GAGCGCGTCCTTTCC | 84749 |
| rs778213821 | snp | A/G | 1.68647e-05 | 0.0029038 | missense | USP30 | GRCh38.p7 | 12:109083038 | ACACTGGAGCTGCAG[A/G]ATGGGCCGGGAGCCC | 84749 |
| rs778218408 | snp | A/G | 1.64822e-05 | 0.00287068 | synonymous-codon, missense, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088335 | TAGTAAGCTCCCGTG[A/G]GCCAGCGGCAGCCTG | 84749 |
| rs778230960 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109075318 | GTATGCAAGAGTTGC[C/T]TTCTCTCCACACCCT | 84749 |
| rs778282405 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109073641 | CTGGTGTTAGAGACT[A/G]CCTGGCCTCTGCACA | 84749 |
| rs778310382 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046245 | TACCTGGGACTACAG[C/G]CACATGCCACCACAC | 84749 |
| rs778324432 | snp | C/T | 1.81079e-05 | 0.00300892 | intron-variant, missense | USP30 | GRCh38.p7 | 12:109083081 | TGTGCGCGCGAGGAG[C/T]CGATGCAGCAGGAAT | 84749 |
| rs778349528 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109058934 | AGAGGGGTGTAACTT[A/C]GTGCCACTTTTCTGG | 84749 |
| rs778350739 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109082117 | TTCTGACTGTATCCA[C/G]TGGGTCTTTTCAGCC | 84749 |
| rs778506378 | in-del | -/G | | | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109021393 | ACTGTAATAGGCACT[-/G]GGGGTATGACAGAAC | 84749 |
| rs778519439 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109068282 | CAGCCACACTTCCAA[A/G]ATGGCCTTGTCCAGC | 84749 |
| rs778544142 | snp | A/G | 1.64904e-05 | 0.00287139 | synonymous-codon, intron-variant | USP30 | GRCh38.p7 | 12:109057954 | CCTTGTTAATTTAGG[A/G]AACACCTGCTTCATG | 84749 |
| rs778556756 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109033790 | GGTAAAGAGGTGAGG[C/G]TTGGTTAAGAGGTTA | 84749 |
| rs778600568 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109069383 | TTCATCTGTACAGGG[C/G]TGCACCTCTGGTGTG | 84749 |
| rs778645281 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109065185 | ATCTTGGGAGTCACT[A/G]AACTTCCAGAAACTG | 84749 |
| rs778692196 | snp | C/T | 1.64939e-05 | 0.0028717 | synonymous-codon | USP30 | GRCh38.p7 | 12:109085850 | GCAGGAGGTCCTGTC[C/T]TCCAGCGCCTACCTG | 84749 |
| rs778722109 | snp | A/C | | | | | GRCh38.p7 | 12:109021601 | TGCCTTCAAGATCCT[A/C]GATAGTTTAATGGTT | 84749 |
| rs778785108 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109040896 | GTGAATTCAGAACAT[C/G]GGGGATCATTGGGGA | 84749 |
| rs778789772 | snp | A/G | 1.64779e-05 | 0.00287031 | intron-variant | USP30 | GRCh38.p7 | 12:109081396 | AGCCGCCACATGGGT[A/G]TGTACTGATTTATGG | 84749 |
| rs778799807 | in-del | -/TGT | 8.24504e-05 | 0.00642016 | intron-variant | USP30 | GRCh38.p7 | 12:109082069 | GCCTGTGTGTGCTGA[-/TGT]AGCGCCTCTCACACC | 84749 |
| rs778802099 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109077706 | TTCTGTTTGTCTTAC[A/G]TATTTTCTTGTTCCT | 84749 |
| rs778802590 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109065464 | GAAGCACAAAGTGTG[A/C]AGGCGGCTGTCTGGG | 84749 |
| rs778889054 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046821 | CCCACCTCAGCCTCC[C/T]GAGTAGCTAGGATTA | 84749 |
| rs778893350 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109079406 | CTTAGCTCTGTCACC[A/G]AGGCTGGATTGCAAT | 84749 |
| rs778943611 | snp | A/G | 3.43749e-05 | 0.00414563 | intron-variant | USP30 | GRCh38.p7 | 12:109084910 | GGTTTTGTTTACAGA[A/G]CCACTGCTAATTTTC | 84749 |
| rs778970053 | snp | C/T | 3.36802e-05 | 0.00410353 | intron-variant | USP30 | GRCh38.p7 | 12:109082799 | ACTCCGTGTATCCTG[C/T]CCCTGAAACAACTCG | 84749 |
| rs778976494 | snp | A/C | 3.29457e-05 | 0.00405854 | missense | USP30 | GRCh38.p7 | 12:109085726 | ATGGAGACATGCACT[A/C]TGGACACTTTGTCAC | 84749 |
| rs779012621 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109029335 | TCAGAGGCACTCTCT[C/T]TGACAGACTAAAAGT | 84749 |
| rs779023968 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109042463 | GCATTTTGCCCATTT[C/T]TCTGCACCCTCCTAT | 84749 |
| rs779034839 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109078947 | CTCCATTTTCTCAGT[C/T]AGTGTCATTTATATC | 84749 |
| rs779097390 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109028086 | CCCAGTGGGTGTGGA[A/G]TGGTCTGATTTGCAT | 84749 |
| rs779209230 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109043136 | CCAAGTCCATGGATT[A/G]GAAGAATTAATATCG | 84749 |
| rs779264708 | snp | A/G | 0.000116043 | 0.0076163 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052647 | GGCGGCGGTAGCGGA[A/G]GAGACGGTTTCAGGC | 84749 |
| rs779280314 | in-del | -/A | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055815 | CAAACCCAGTGCATT[-/A]AAAAAAAAAAAAAAG | 84749 |
| rs779288538 | snp | C/G | 6.68975e-05 | 0.0057831 | intron-variant | USP30 | GRCh38.p7 | 12:109072270 | AGGGATTATAGTAAG[C/G]TTTTCAGTCTGTTTT | 84749 |
| rs779299397 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109056040 | AGAGGGAACAGCAGT[A/G]CAAACGCCTTGAGGT | 84749 |
| rs779332885 | snp | C/T | 1.65748e-05 | 0.00287874 | synonymous-codon | USP30 | GRCh38.p7 | 12:109082681 | GAAGCCAAGGGAACG[C/T]TGAACGGGGAAAAGG | 84749 |
| rs779354955 | snp | C/T | 0.000463407 | 0.0152148 | intron-variant | USP30 | GRCh38.p7 | 12:109072293 | TCTGTTTTTTTTTTT[C/T]CTCCCCTACAGCAGC | 84749 |
| rs779362326 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109058856 | TTTTTGCCTGTCAGC[A/G]AAGATTAAAAAACAA | 84749 |
| rs779395572 | snp | A/G | 1.71622e-05 | 0.0029293 | intron-variant | USP30 | GRCh38.p7 | 12:109058137 | AATTTCAAGGGAATT[A/G]TGTACCTTTTCAAAG | 84749 |
| rs779444244 | snp | A/G | 1.69375e-05 | 0.00291006 | synonymous-codon | USP30 | GRCh38.p7 | 12:109083046 | GCTGCAGGATGGGCC[A/G]GGAGCCCCCACACCA | 84749 |
| rs779452744 | snp | A/G | 0.000149732 | 0.00865121 | intron-variant | USP30 | GRCh38.p7 | 12:109072372 | GTTTTCCATTGAAAT[A/G]TAACACATAAGATGT | 84749 |
| rs779601007 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109059967 | ATGTAGATATCAAAC[A/G]GAATCATTAAGCAAT | 84749 |
| rs779618510 | in-del | -/TTGTTT | | | intron-variant | USP30 | GRCh38.p7 | 12:109056200 | TTGTTGTTGTTGTTG[-/TTGTTT]TTTATGAGACTGAGT | 84749 |
| rs779647885 | in-del | -/C | 1.65302e-05 | 0.00287486 | frameshift-variant | USP30 | GRCh38.p7 | 12:109085007 | TGAATGGCGCCTGCT[-/C]CCCATCTTTATTGCC | 84749 |
| rs779656402 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053344 | AAAGGCCCTTGTTTT[G/T]CAAGGGTCTCTAAAT | 84749 |
| rs779754508 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109032311 | TGTCTAAAAAACAAA[A/G]TAAATGCTCTATGCA | 84749 |
| rs779780380 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109031121 | ACATACTTTTGAGCC[A/G]TCTTAATATAGTATA | 84749 |
| rs779822660 | snp | C/T | 4.95274e-05 | 0.00497607 | intron-variant | USP30 | GRCh38.p7 | 12:109072298 | TTTTTTTTTTTCTCC[C/T]CTACAGCAGCAGTCA | 84749 |
| rs779829679 | snp | C/T | 1.65373e-05 | 0.00287548 | synonymous-codon | USP30 | GRCh38.p7 | 12:109085866 | TCCAGCGCCTACCTG[C/T]TGTTCTACGAGCGCG | 84749 |
| rs779891373 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109039759 | GGGACTACAGGTGCC[C/T]GCCACCACACCCAGT | 84749 |
| rs779918926 | snp | A/G | 3.81964e-05 | 0.00436998 | intron-variant, synonymous-codon | USP30 | GRCh38.p7 | 12:109083106 | AGGAATTTTCAGCAC[A/G]GAGAAAAGCAGTTTG | 84749 |
| rs779939553 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109069075 | ACAGATGGAAAAACA[C/T]TGAGGCTCAGAGAAG | 84749 |
| rs779948971 | snp | C/T | 0.000312961 | 0.0125053 | synonymous-codon, intron-variant | USP30 | GRCh38.p7 | 12:109057996 | ACAAGGCCTGTCTGC[C/T]TGTCCTGCTTTCATC | 84749 |
| rs779958313 | in-del | -/C | 1.6571e-05 | 0.0028784 | frameshift-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088469 | GGGCCAGTTCTCTTT[-/C]ATCATCTCGGTGCTC | 84749 |
| rs780041215 | snp | A/G | 1.64855e-05 | 0.00287097 | missense, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088315 | TTGGTCGGGTGGTTC[A/G]TCATTAGTAAGCTCC | 84749 |
| rs780076167 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054836 | TGCATATTCTGTTGA[C/T]TCTGTCTTGGAAAAC | 84749 |
| rs780105745 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109026964 | ATAAGGGCACTATCT[C/T]ATCATGTCAGCCCCA | 84749 |
| rs780108568 | snp | A/C | 1.6473e-05 | 0.00286988 | stop-gained | USP30 | GRCh38.p7 | 12:109081979 | ACCACTTCATCTCAT[A/C]AGAATCAGTGCGGGA | 84749 |
| rs780117191 | snp | A/C/G | 3.33251e-05 | 0.00408187 | intron-variant | USP30 | GRCh38.p7 | 12:109071595 | ACCTCTCTAAAGAAT[A/C/G]CTTTGCCCTATGACA | 84749 |
| rs780131121 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109062953 | TTAAGTCATGAGTTT[A/C]CTCATATTTATAAGA | 84749 |
| rs780150316 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109073777 | TTGAGTCCAGTGGTT[A/G]AGTCTATGCTCATGG | 84749 |
| rs780186258 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109075708 | GTGATAGCTCTTTAT[G/T]GTTTTATTTGCATTT | 84749 |
| rs780231534 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109040779 | GCTTTTCCCAGAGCA[A/C]GTGTTTCAAGAAAAA | 84749 |
| rs780237976 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109058334 | CCAGTACTTTAGGAG[A/G]CCAAGGCAGGTGGAT | 84749 |
| rs780238013 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109025610 | ATATGAGTATCTCAT[A/T]TAGAAATTTGCCTGT | 84749 |
| rs780243120 | snp | A/G | | | synonymous-codon | USP30 | GRCh38.p7 | 12:109067612 | CAGATGGCAGATCTC[A/G]TCATTTGAAGAACAG | 84749 |
| rs780268603 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109028019 | CCCACCAGCAATGCA[C/G]AAGGATTCCAATTTC | 84749 |
| rs780421386 | in-del | -/A | | | intron-variant | USP30 | GRCh38.p7 | 12:109035336 | TACCATTACCATTTC[-/A]AATTTGTTTATTTAT | 84749 |
| rs780430827 | snp | C/G | 1.71734e-05 | 0.00293026 | intron-variant, missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052733 | GACAGGGCCATCCAG[C/G]GCTTCCTGCGGACCG | 84749 |
| rs780435739 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109084813 | AGGGCAGATTATTTT[A/G]TGAATCTATATAATA | 84749 |
| rs780515923 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109071343 | GAGGTCAAGGCTGTC[G/T]CAGTGAAACAGAATG | 84749 |
| rs780518472 | snp | C/T | 0.000201059 | 0.0100244 | intron-variant | USP30 | GRCh38.p7 | 12:109072394 | ATAAGATGTGGACTT[C/T]TAAGATATGATAATA | 84749 |
| rs780525694 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109065201 | AACTTCCAGAAACTG[C/T]ACTGAGAGGCAGGCT | 84749 |
| rs780574246 | in-del | -/AG | | | intron-variant | USP30 | GRCh38.p7 | 12:109071985 | TTAATACAGGGGAAC[-/AG]GGGCCATAGGAATGC | 84749 |
| rs780601311 | snp | C/T | 3.18578e-05 | 0.00399097 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052811 | CGGGACCAGGGTCCC[C/T]AGCTTGGGCCCGTGA | 84749 |
| rs780624324 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109058681 | ATAAACAGTTTCATC[A/G]TAAGAAGTATTCTGG | 84749 |
| rs780714512 | snp | C/T | 1.67421e-05 | 0.00289323 | intron-variant | USP30 | GRCh38.p7 | 12:109073545 | CAGGTAAATACAATA[C/T]CAACACTTGATATTT | 84749 |
| rs780722140 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109044172 | GAGTAGTTGAATAAA[C/T]AGAGACAAAATGTAG | 84749 |
| rs780738235 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109024509 | GCAATCAACCTGCCT[C/T]GGCCTCCCAAAGTGC | 84749 |
| rs780748622 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109072114 | TTTCTATTGCATTTG[A/G]TGAAAGAATATTCAT | 84749 |
| rs780761713 | in-del | -/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109034506 | CTGAGGTGGGAGGAT[-/C]GCTTGAGCTCATGAG | 84749 |
| rs780778573 | snp | C/T | 1.74964e-05 | 0.00295769 | intron-variant | USP30 | GRCh38.p7 | 12:109073413 | GGGCTAAAAGTGACA[C/T]ATCAAAAAACTTTTT | 84749 |
| rs780800915 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109066656 | CGCCATTGCACTCCA[C/T]CCTGGGCGACAGAGC | 84749 |
| rs780847885 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109030939 | CTTTTACAATGTACA[C/G]ATATATCAAATCATC | 84749 |
| rs780870861 | in-del | -/TGAAAG | 0.00204252 | 0.0318918 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053995 | CTTCTGCTATAAAAA[-/TGAAAG]TGATAGTAGAACCTG | 84749 |
| rs780950848 | snp | A/T | 3.39974e-05 | 0.00412281 | intron-variant | USP30 | GRCh38.p7 | 12:109085119 | AGCTACCACTGCTCT[A/T]AGCTTCTAAAATTAG | 84749 |
| rs780966277 | snp | G/T | 1.64738e-05 | 0.00286995 | missense, utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109067574 | TTAGATGCAAGCTGC[G/T]TGTTGGATGTCTTAA | 84749 |
| rs781003813 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055067 | GTAACATATATGCAG[A/G]TACACATTACATAGC | 84749 |
| rs781072186 | snp | C/T | 1.66313e-05 | 0.00288364 | synonymous-codon | USP30 | GRCh38.p7 | 12:109082671 | ATTTCAGATTGAAGC[C/T]AAGGGAACGTTGAAC | 84749 |
| rs781073710 | snp | C/T | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | USP30, USP30-AS1 | GRCh38.p7 | 12:109052290 | AGCAGAGGCCTGACC[C/T]GACTTTCGGCTGTTG | 84749 |
| rs781093838 | snp | A/G | | | utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109025068 | AGAACAGAAACAGAG[A/G]AAAGGTGAGTTGATC | 84749 |
| rs781093882 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109029618 | TTCCACCCTCCCTCC[A/G]TGCCTGAGCTATCTT | 84749 |
| rs781137693 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109080554 | TGCAATGAATAATCT[A/G]ACATGAACATCTTTC | 84749 |
| rs781152880 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109067816 | TACAGCTGTTTTTCA[C/T]TCAGTGGATGGAAGG | 84749 |
| rs781178610 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109039564 | AACTGATCTAGTTCC[C/T]GAGAAAAAATGTGGG | 84749 |
| rs781192500 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109068374 | CCAAAACTGTGGGGC[C/T]GACGTGAGGGGCATC | 84749 |
| rs781203154 | snp | C/T | 3.30732e-05 | 0.00406638 | missense | USP30 | GRCh38.p7 | 12:109082996 | CCTAGTCAACACAAC[C/T]CTAAACTGAACAAGA | 84749 |
| rs781203229 | snp | G/T | 1.66297e-05 | 0.0028835 | intron-variant | USP30 | GRCh38.p7 | 12:109071600 | TCTAAAGAATGCTTT[G/T]CCCTATGACAGGATG | 84749 |
| rs781225421 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109080877 | TAGCTAGACAGTATA[A/G]CCTAGGTGTGTAGTA | 84749 |
| rs781253840 | snp | A/T | 0.000165382 | 0.00909196 | intron-variant | USP30 | GRCh38.p7 | 12:109067474 | GCAAGTTTTCTGGTT[A/T]GTTGTTATGCTGATG | 84749 |
| rs781296533 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109025791 | CAGCCCAGCTCTAGC[A/G]ATTCTCCCACCTCAG | 84749 |
| rs781314551 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109083590 | ACATGGAGGCTCCAC[A/G]GGGTTGAATGATTGG | 84749 |
| rs781373755 | in-del | -/AT | | | intron-variant | USP30 | GRCh38.p7 | 12:109041879 | CACAACCAGAAAAAA[-/AT]AGTTTGAATTACAAA | 84749 |
| rs781378855 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109074163 | CTTCTTTCATTTAGC[A/G]TAATATTTCCACGTT | 84749 |
| rs781400190 | snp | A/G | 1.64914e-05 | 0.00287149 | synonymous-codon | USP30 | GRCh38.p7 | 12:109071671 | TGAGCGAGACCGCCA[A/G]CCTCGGGTCACACAT | 84749 |
| rs781404146 | snp | A/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109087700 | AGAAAGATAGAGAAA[A/T]GGGGCTGAGCCTTGG | 84749 |
| rs781445957 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109064325 | ACTGGAGTGCAGTGA[C/T]GCAATCTCAGCTCAC | 84749 |
| rs781476026 | snp | C/T | 1.65373e-05 | 0.00287548 | missense, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088271 | CCAGAACCTTCTTTC[C/T]CACGGGAAGACTGTG | 84749 |
| rs781580249 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109026837 | AGTATAGTTAGGTTC[C/T]GGTGAGGGCTCTCTT | 84749 |
| rs781613339 | snp | C/T | 3.29663e-05 | 0.00405981 | missense, synonymous-codon, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088331 | TCATTAGTAAGCTCC[C/T]GTGGGCCAGCGGCAG | 84749 |
| rs781623621 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109083534 | TCAGCTGAGGTCTCA[G/T]TTAAGCCGGGTAGCT | 84749 |
| rs781640914 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109063694 | CCAGTTTCTCCTCAC[C/T]AACAGATATTATTTT | 84749 |
| rs781720297 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109032136 | AACATGGTGAAACCC[A/G]TCTCTACAAAAAAAA | 84749 |
| rs781732222 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109062846 | CGTACTGAAACTGTA[C/T]CCATGAAACAGTAAC | 84749 |
| rs781764916 | snp | A/G/T | 0.000116116 | 0.00761885 | missense, intron-variant | USP30 | GRCh38.p7 | 12:109056783 | CAGAAAGAAAGAAGC[A/G/T]TAGAAAAGGTAAGAA | 84749 |
| rs796065931 | in-del | -/TG | | | intron-variant | USP30 | GRCh38.p7 | 12:109081618 | ATACACACGCACGCA[-/TG]CGCGCACACACACAC | 84749 |
| rs796245683 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109028451 | GGAGGTGCCACACCC[-/T]TTTTTTTTTTCTGTT | 84749 |
| rs796284081 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109059981 | CAGAATCATTAAGCA[A/G]TCACCTGTGGCCATA | 84749 |
| rs796529752 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109028452 | GGAGGTGCCACACCC[-/T]TTTTTTTTTCTGTTT | 84749 |
| rs796586745 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109076732 | AGTGATTGATTTTTT[C/T]TTTTTTTTTTTTTTT | 84749 |
| rs796617389 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109070421 | GGATAGGAGGTAGCC[A/G]TGCGAAGGTCTGAGC | 84749 |
| rs796850851 | in-del | -/A | | | intron-variant | USP30 | GRCh38.p7 | 12:109044705 | GTACTTTGCCACAAT[-/A]AAAAAAAATGGAAAA | 84749 |
| rs796964527 | in-del | -/T | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046430 | GTCTTTTTTTTTTTT[-/T]CTTCCTCTTCAGGCC | 84749 |