SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs15186 | snp | A/T | 0 | 0 | synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088278 | CTTCTTTCTCACGGG[A/T]AGACTGTGGTACCAG | 84749 |
rs706493 | snp | A/G | 0.000164954 | 0.00908018 | synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088296 | CCACCCGACCAACAC[A/G]CACTGGTACCACAGT | 84749 |
rs1059257 | snp | A/G | 0.257454 | 0.249889 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109087634 | TACTGCAAAGCTGTA[A/G]CTTTAAGTAATTGCT | 84749 |
rs1059262 | snp | G/T | 0.306431 | 0.243548 | intron-variant, utr-variant-3-prime, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109087930 | TTAAACTAGTAGTTT[G/T]GCCATAATAACTGCT | 84749 |
rs1368556 | snp | C/T | 0.36315 | 0.222928 | intron-variant | USP30 | GRCh38.p7 | 12:109032515 | AGAACCTTAAGAACA[C/T]TGTGTTAGGTGAAAC | 84749 |
rs1433314 | snp | A/C | 0.36315 | 0.222928 | intron-variant | USP30 | GRCh38.p7 | 12:109031449 | GACAGTTTCTTTAAA[A/C]GTTAAACATAGAATT | 84749 |
rs1433315 | snp | A/T | 0.36315 | 0.222928 | intron-variant | USP30 | GRCh38.p7 | 12:109031501 | TTCCACTCCTAGGTA[A/T]ATACAAAAAGAATTA | 84749 |
rs1433316 | snp | A/T | 0.156319 | 0.231784 | intron-variant | USP30 | GRCh38.p7 | 12:109034163 | CCACAATATTGTGAC[A/T]TGTACCTCGTGTTTT | 84749 |
rs1433317 | snp | C/T | 0.494187 | 0.0535994 | intron-variant | USP30 | GRCh38.p7 | 12:109034171 | TTGTGACTTGTACCT[C/T]GTGTTTTTATTTTTA | 84749 |
rs1982093 | snp | G/T | 0 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109071103 | AGAGATAAAGAATGG[G/T]GGGTGCCAGGGGTTG | 84749 |
rs2018290 | snp | A/C | 0.455621 | 0.142197 | intron-variant | USP30 | GRCh38.p7 | 12:109030698 | cttggctcactgcaa[A/C]ctctgcctcccaggt | 84749 |
rs2304266 | snp | C/T | 0.294832 | 0.245947 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052596 | CGCAGGTTCCGCTGT[C/T]TCGGGAACCGTCGTA | 84749 |
rs2304267 | snp | C/T | 0.313767 | 0.241731 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052796 | GGCTGCCGAAGAGGC[C/T]GGGACCAGGGTCCCC | 84749 |
rs3217401 | in-del | -/CGG | | | intron-variant, cds-indel, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052637 | CGGCGGCGGCGGCGG[-/CGG]TAGCGGAGGAGACGG | 84749 |
rs3742028 | snp | A/G | 0.496382 | 0.0423778 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053663 | CCCATTCCGTAGATA[A/G]GAAGTGTGGCCCCAT | 84749 |
rs3742029 | snp | A/G | 0.0584853 | 0.160693 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109086427 | CACGTCCATTGTGAA[A/G]TATTCCTTCCAGGCT | 84749 |
rs4296113 | snp | C/T | 0.358303 | 0.225323 | intron-variant | USP30 | GRCh38.p7 | 12:109036454 | tacaggtgtgaacca[C/T]gcccagctaattttt | 84749 |
rs4309234 | snp | C/T | 0.239037 | 0.24976 | intron-variant | USP30 | GRCh38.p7 | 12:109037899 | gccttctcaggttta[C/T]cctgagcatgtagag | 84749 |
rs4388979 | snp | G/T | 0.483563 | 0.0891524 | intron-variant | USP30 | GRCh38.p7 | 12:109037207 | tctgctgttgtgctc[G/T]ctagtgaatttttca | 84749 |
rs6606733 | snp | A/G | 0.232943 | 0.249417 | intron-variant | USP30 | GRCh38.p7 | 12:109050426 | CAATCCTTTTTAAGC[A/G]TACAAAGAGATCCGG | 84749 |
rs6606735 | snp | C/T | 0.456685 | 0.140646 | intron-variant, upstream-variant-2KB, downstream-variant-500B | USP30, USP30-AS1 | GRCh38.p7 | 12:109051638 | gcagtggcatgatct[C/T]ggctcagtgcaacct | 84749 |
rs6606740 | snp | A/G | 0.381113 | 0.21286 | intron-variant | USP30 | GRCh38.p7 | 12:109075350 | ggcaacacttgttac[A/G]tgctgtctttttttt | 84749 |
rs7135644 | snp | A/G | 0.252421 | 0.249988 | intron-variant | USP30 | GRCh38.p7 | 12:109038183 | ccgacccctccaaag[A/G]ccccagtgtatgttg | 84749 |
rs7137083 | snp | A/G | 0.295088 | 0.245901 | intron-variant | USP30 | GRCh38.p7 | 12:109056091 | TTCCATGTGGAAGTG[A/G]AGTGAGAGGCAGAAA | 84749 |
rs7138838 | snp | C/T | 0.252702 | 0.249985 | intron-variant | USP30 | GRCh38.p7 | 12:109038211 | ttggttcccgccccc[C/T]tccccacctgccagt | 84749 |
rs7296509 | snp | C/T | 0.306927 | 0.243432 | intron-variant | USP30 | GRCh38.p7 | 12:109084607 | CAGCCAAAACCATCA[C/T]GGTGCTGCTGTTGAG | 84749 |
rs7302579 | snp | A/T | 0.306679 | 0.24349 | intron-variant | USP30 | GRCh38.p7 | 12:109060875 | gctctcgaactcctg[A/T]cctcaagtggtgcac | 84749 |
rs7307927 | snp | C/T | 0.286042 | 0.247388 | intron-variant | USP30 | GRCh38.p7 | 12:109058989 | atagcttgcgaaata[C/T]tcagtactgtttgac | 84749 |
rs7316006 | snp | A/T | 0 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109063903 | tttttttttgagaag[A/T]cagtctgttgccagg | 84749 |
rs7316260 | snp | C/T | 0.310386 | 0.242597 | intron-variant | USP30 | GRCh38.p7 | 12:109060865 | tcaccaggctgctct[C/T]gaactcctgacctca | 84749 |
rs7485962 | snp | A/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | USP30, USP30-AS1 | GRCh38.p7 | 12:109054539 | tgtctcaaaaaaaaa[A/T]aaaaataaaaataag | 84749 |
rs7955458 | snp | C/T | 0.251578 | 0.249995 | utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109047643 | CAAGCTCTGCATATT[C/T]GAAGTGTTGCAAACT | 84749 |
rs7957021 | snp | A/G | 0.262159 | 0.249704 | intron-variant | USP30 | GRCh38.p7 | 12:109075764 | ccttttcatataccc[A/G]ctggccatttgtatg | 84749 |
rs7961606 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | USP30 | GRCh38.p7 | 12:109080928 | tgtaagcgcgctctg[C/T]gatgtttacacaatg | 84749 |
rs7961975 | snp | C/T | 0.232943 | 0.249417 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109051106 | atgttgcccaggtgg[C/T]cttggactctgggcc | 84749 |
rs7963952 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | USP30 | GRCh38.p7 | 12:109036810 | gtcagtcttattaag[G/T]ataccttttatgtga | 84749 |
rs7965921 | snp | A/G | 0.361684 | 0.223667 | intron-variant | USP30 | GRCh38.p7 | 12:109078556 | GTGAGCCGAGATCAC[A/G]CCACTGCATGCCAGC | 84749 |
rs7965956 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055395 | atatatatatatata[C/T]atatatttttttttt | 84749 |
rs7967169 | snp | C/G | 0.323671 | 0.238899 | intron-variant | USP30 | GRCh38.p7 | 12:109032690 | TGCTAATACATATGA[C/G]GACTCTTTTAGAAGG | 84749 |
rs7967182 | snp | C/T | 0.141596 | 0.225274 | intron-variant | USP30 | GRCh38.p7 | 12:109073339 | AAGAATATTTTTTCT[C/T]AAGAGGTAGTTTCTA | 84749 |
rs7967285 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109040081 | ATTGTTTTTTTTCTA[C/T]ATGTGAAAACAGTTT | 84749 |
rs7967322 | snp | C/T | 0.271943 | 0.249035 | synonymous-codon | USP30 | GRCh38.p7 | 12:109073451 | AGGGTCACCTCACCC[C/T]ACATCCAATCACTGG | 84749 |
rs7970728 | snp | C/G | 0.0744748 | 0.178019 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046526 | aatttaaatgttaat[C/G]tcatccaaaaaccat | 84749 |
rs7972579 | snp | G/T | 0.0726307 | 0.176182 | intron-variant | USP30 | GRCh38.p7 | 12:109034966 | ggttgctgtttgaat[G/T]ataccactttttcca | 84749 |
rs7973633 | snp | C/T | 0.0836354 | 0.186609 | intron-variant | USP30 | GRCh38.p7 | 12:109027073 | catatacatttgggg[C/T]ggacacaaacattca | 84749 |
rs7978342 | snp | C/T | 0.587129 | 0.156226 | intron-variant | USP30 | GRCh38.p7 | 12:109078285 | AAAAATTAGCTGGGC[C/T]TGGTGGCGGGCGTCT | 84749 |
rs7979475 | snp | C/T | 0.247905 | 0.249991 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046401 | tacgggcgtgagcca[C/T]tgcacccagcccagt | 84749 |
rs9668445 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055379 | ACACACATATATATA[C/T]ATATATATATATATA | 84749 |
rs9668456 | snp | C/T | 0.498774 | 0.02473 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055623 | CAGGCTGGTCTCCCA[C/T]TGACCTCAGGTGATC | 84749 |
rs10525667 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055402 | tatatatatatatat[A/T]ttttttttttttttt | 84749 |
rs10582659 | in-del | -/ACAC | 0.0905309 | 0.192535 | intron-variant | USP30 | GRCh38.p7 | 12:109081605 | TTTGGCTTTTTGAAT[-/ACAC]ACGCACGCATGCGCG | 84749 |
rs10774646 | snp | A/G | 0.491104 | 0.0660973 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022236 | ATGAAAAGAAAAGCT[A/G]GAAAATTATACAACA | 84749 |
rs10774647 | snp | A/G | 0.490997 | 0.0664859 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022306 | GCTATGAGAATGACC[A/G]TTGAATGGACACTTA | 84749 |
rs10774825 | snp | A/G | 0.232359 | 0.249377 | intron-variant | USP30 | GRCh38.p7 | 12:109058369 | AGGTCAGGAGTTCGA[A/G]ACCAGCCTGACCAAC | 84749 |
rs10774928 | snp | C/T | 0.495445 | 0.0475058 | intron-variant | USP30 | GRCh38.p7 | 12:109077137 | TGATTTGCTAATATT[C/T]CCTAAAGGATATTAG | 84749 |
rs10774961 | snp | A/G | 0.499234 | 0.0195537 | intron-variant | USP30 | GRCh38.p7 | 12:109080328 | GGAAAAAAAGCCACA[A/G]ACACACAAATCTCGC | 84749 |
rs10850069 | snp | C/G | 0.359862 | 0.224567 | intron-variant | USP30 | GRCh38.p7 | 12:109028863 | ATGAAGGATCCACCC[C/G]CATGATCCAAACACC | 84749 |
rs10850309 | snp | A/G | 0.252702 | 0.249985 | intron-variant | USP30 | GRCh38.p7 | 12:109045226 | TCGGGTGATCCACCC[A/G]CCTCGGCCTCCCAAA | 84749 |
rs10850337 | snp | G/T | 0.498794 | 0.0245311 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046321 | CGTTTCACCATGTTG[G/T]CCAGGATGGTCTCGA | 84749 |
rs10850362 | snp | A/G | 0.495671 | 0.0463237 | intron-variant | USP30 | GRCh38.p7 | 12:109048784 | AAAGAAAAACCGGAT[A/G]TAAAACAGTTTATTC | 84749 |
rs10850589 | snp | C/T | 0.496937 | 0.0390173 | intron-variant | USP30 | GRCh38.p7 | 12:109061685 | agagtgctgggattg[C/T]ggacatgagccacca | 84749 |
rs10850688 | snp | A/G | 0.166832 | 0.235761 | intron-variant | USP30 | GRCh38.p7 | 12:109068664 | CTTGGAGATTTAGTC[A/G]CCAAGGACATCAGAT | 84749 |
rs10850717 | snp | G/T | 0.25912 | 0.249834 | intron-variant | USP30 | GRCh38.p7 | 12:109070043 | TGCAGGGACTAGGAG[G/T]CTGCGGGCGGCATCA | 84749 |
rs10850840 | snp | G/T | 0.348555 | 0.229754 | intron-variant | USP30 | GRCh38.p7 | 12:109077825 | CTTGTGTGTTTGTGT[G/T]GGGGGGGGAGGGTGT | 84749 |
rs11066507 | snp | C/T | 0.34989 | 0.229177 | intron-variant | USP30 | GRCh38.p7 | 12:109034106 | ACAAAAACAGCTCAA[C/T]GTGTCTGAGTCGTTG | 84749 |
rs11066540 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | USP30 | GRCh38.p7 | 12:109035605 | TTGGCCTAGTGATCC[A/G]CCCACCTCGGCCTCC | 84749 |
rs11066775 | snp | A/C | 0.0923359 | 0.194016 | intron-variant | USP30 | GRCh38.p7 | 12:109040510 | tatcccacacagttt[A/C]tgtgagtcaggaatc | 84749 |
rs11066777 | snp | C/T | 0.216048 | 0.247684 | intron-variant | USP30 | GRCh38.p7 | 12:109040547 | GAGCAGCTGAGTTGG[C/T]TGGCTATTGCTCAGG | 84749 |
rs11066984 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | USP30 | GRCh38.p7 | 12:109044258 | GGTACAGAATTTTAG[C/T]TTTGCAGATGGAGAG | 84749 |
rs11067125 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046854 | GGTGTGCGCCATCAT[A/C/G]CCCAGCTAATTTTTG | 84749 |
rs11067210 | snp | A/G/T | 0.0058479 | 0.0537564 | intron-variant | USP30 | GRCh38.p7 | 12:109048438 | CATCAGTGATTGCCA[A/G/T]GGGTTGAAGGGGGGT | 84749 |
rs11067292 | snp | A/G | 0.498611 | 0.0263212 | intron-variant | USP30 | GRCh38.p7 | 12:109050017 | caagatatgccGggc[A/G]gggcacggtggctca | 84749 |
rs11067385 | snp | A/G | 0.0104769 | 0.0716149 | intron-variant, missense, nc-transcript-variant, utr-variant-5-prime, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052697 | CTGAGCTCCCGGGCC[A/G]AGGCGGCGATGACCG | 84749 |
rs11067924 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP30 | GRCh38.p7 | 12:109063773 | TTTGCATTTCCCTAA[C/T]GATAAGTTATATTGA | 84749 |
rs11068203 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | USP30 | GRCh38.p7 | 12:109070677 | CTGTGTTGTGACCCC[A/G]TTACTCCCGGAAGAG | 84749 |
rs11068498 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | USP30 | GRCh38.p7 | 12:109076793 | CTGGAGTGCAGTGGC[A/G]TGATCTCGGCTCACT | 84749 |
rs11068637 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | USP30 | GRCh38.p7 | 12:109079339 | TTTTCTTTTCTTTTT[C/T]TTTTTTTTTTTCTTT | 84749 |
rs11068749 | snp | A/G | 0.430732 | 0.172731 | intron-variant | USP30 | GRCh38.p7 | 12:109081625 | CGCACGCATGCGCGC[A/G]CACACACACACACAC | 84749 |
rs11068750 | snp | A/G | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109081627 | CACGCATGCGCGCAC[A/G]CACACACACACACAC | 84749 |
rs11351379 | in-del | -/T | 0.236724 | 0.249647 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109047170 | ACAGAGGTGGATGCA[-/T]TTTTTTTTTTTAACC | 84749 |
rs11611432 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055460 | caggctggagtgcag[G/T]ggcgcaatctgggct | 84749 |
rs11611623 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109080621 | tagtgtttcattctg[G/T]ggacatgccatataa | 84749 |
rs11829521 | snp | A/C | 0.0718919 | 0.175435 | intron-variant | USP30 | GRCh38.p7 | 12:109043597 | tgggtaaataccaaa[A/C]tgcaagacctaaaat | 84749 |
rs11830671 | snp | A/C | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | USP30, USP30-AS1 | GRCh38.p7 | 12:109054677 | atttaatcctcacaa[A/C]agccctatgaggtag | 84749 |
rs11832964 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046195 | aacctccgccccccc[C/G]ggtttaagtgattcc | 84749 |
rs11836795 | snp | C/G | 0.00716266 | 0.059414 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109087500 | TGCAAGGGGCAGCTT[C/G]AACTGTACGGTCCGT | 84749 |
rs11837724 | snp | A/T | 0.100231 | 0.200173 | intron-variant | USP30 | GRCh38.p7 | 12:109043615 | caagacctaaaatga[A/T]aaaactcttggaaaa | 84749 |
rs12229459 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109076893 | cccgccaccacgccc[A/G]gctaattttttgtat | 84749 |
rs12306731 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055385 | atatatatacatata[C/T]atatatatatatata | 84749 |
rs12307368 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046122 | tttttttttttttta[A/G]atggagtctcactct | 84749 |
rs12307634 | snp | A/G | 0.00760445 | 0.0611915 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046558 | tcacagaaacatcca[A/G]actaatgtctgacca | 84749 |
rs12308752 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | USP30 | GRCh38.p7 | 12:109080766 | tggtacggtaccttt[C/T]ctgtttttagataca | 84749 |
rs12309096 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109051277 | tttttttttttttga[A/T]gctgaatctctctct | 84749 |
rs12309678 | snp | C/T | 0.25912 | 0.249834 | intron-variant | USP30 | GRCh38.p7 | 12:109064568 | TACAGGCGTAGACCA[C/T]TGCACCTGGCCTCAT | 84749 |
rs12312381 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109023711 | caatctcggctcact[A/G]ctacctccacctccc | 84749 |
rs12314002 | snp | A/C | 0 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109031320 | cctcaatggcattgt[A/C]tttgtcatgctggat | 84749 |
rs12316216 | snp | A/G | 0.252421 | 0.249988 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055850 | gaaaaaaaaCATAGC[A/G]AATAGGTTAATTTTA | 84749 |
rs12317002 | snp | A/G | 0.173643 | 0.238054 | upstream-variant-2KB, utr-variant-5-prime | USP30, SVOP | GRCh38.p7 | 12:109021143 | GCCCTTCTGCTTGGA[A/G]GAGTTCACAGGCTCT | 84749 |
rs12321746 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | USP30 | GRCh38.p7 | 12:109064560 | gctgggattacaggc[A/G]tagaccactgcacct | 84749 |
rs12368871 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055397 | atatatatatatata[C/T]atatttttttttttt | 84749 |
rs12426673 | snp | G/T | 0.495483 | 0.0473088 | intron-variant, upstream-variant-2KB, nc-transcript-variant | USP30, USP30-AS1 | GRCh38.p7 | 12:109052491 | GAAAGGACGTGGTCC[G/T]TCAGCTATTGCTCTC | 84749 |
rs12809163 | snp | C/T | 0.067446 | 0.170804 | intron-variant | USP30 | GRCh38.p7 | 12:109071445 | TTGAGGGTCTTCACT[C/T]GTGACAGTGTCCAGG | 84749 |
rs12812818 | snp | A/T | 0.0240643 | 0.107019 | intron-variant | USP30 | GRCh38.p7 | 12:109027282 | ttctactttcttttt[A/T]atttttattttttag | 84749 |
rs12812997 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109027319 | ggtctcactctgctg[C/T]ccaggttgacgtgca | 84749 |
rs12813923 | snp | A/G | 0.0232847 | 0.105357 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053454 | TGGGTCCCCAATCCT[A/G]TCAGGGCCCCCATTT | 84749 |
rs12815117 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | USP30 | GRCh38.p7 | 12:109039674 | gtagttcagtggcac[A/G]atctcagctcactgc | 84749 |
rs12815131 | snp | C/T | 0 | 0 | intron-variant, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053718 | AGGAGAAGCCAGATC[C/T]TTTCATCCGCAGGCC | 84749 |
rs12817656 | snp | G/T | 0 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109049023 | actcagtgtttaagg[G/T]ttcttgaaggtcccc | 84749 |
rs12818096 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109079350 | ttttctttttttttt[C/T]ctttttttttttttt | 84749 |
rs12818115 | snp | G/T | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109079381 | ttttttttttttttg[G/T]gacaggggtcttagc | 84749 |
rs12823288 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109033830 | TAAATAATGTAAAGG[G/T]GCACAACTTTAAGGA | 84749 |
rs12824214 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109027343 | acgtgcagtgatgca[A/T]tcacggctcactgca | 84749 |
rs12826751 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055195 | AAAAGCATAACCAGC[A/G]TTCAAGTCAAGCCTG | 84749 |
rs12827122 | snp | A/G | 0 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109033781 | ACAGAAGCTGGTAAA[A/G]AGGTGAGGCTTGGTT | 84749 |
rs13377980 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109035488 | cctgcctcagcctcc[C/T]gagtagttgggacta | 84749 |
rs16939885 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | USP30 | GRCh38.p7 | 12:109068318 | GTAGGCGTTGTCTGC[C/T]GCCACTATCCAGAGA | 84749 |
rs16939892 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | USP30 | GRCh38.p7 | 12:109070256 | TGAGAGTCCTCAGGA[A/G]TTTAGGGCGTATTTT | 84749 |
rs16939904 | snp | A/G | 0.130851 | 0.219781 | missense | USP30 | GRCh38.p7 | 12:109082964 | ACATTTACAAGTACC[A/G]CCTCCTTGGACATAA | 84749 |
rs33962311 | snp | C/T | 0.0201774 | 0.0983961 | missense, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088384 | GAGGGGCTTTTCCCA[C/T]GGGAATCCTTATGCC | 84749 |
rs34221615 | in-del | -/T | 0 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109075858 | TTTTTTTTTTTTTTT[-/T]GCTGTTGGTCCATAT | 84749 |
rs34258926 | in-del | -/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109033229 | ATTTGAGAAGGAAGA[-/C]ATTATACTTCAAGGC | 84749 |
rs34308344 | in-del | -/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109058293 | TCAAAGATGGAGGCC[-/G]GGTGCAGTGGCTCAT | 84749 |
rs34327153 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | USP30 | GRCh38.p7 | 12:109079464 | AACCTCCCAGGCTCA[A/G]GTTATCCTCCCACCT | 84749 |
rs34418635 | in-del | -/TT | | | intron-variant | USP30 | GRCh38.p7 | 12:109044989 | GTAAGGTCAAACATC[-/TT]TTTTTTTTTTTTTTT | 84749 |
rs34459674 | in-del | -/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109073991 | ATAACATTTTCATTG[-/C]CCCCTAAAGAAACTC | 84749 |
rs34629352 | in-del | -/T | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046093 | TGGGGGAAGTCAGTC[-/T]TTTTTTTTTTTTTTT | 84749 |
rs34715237 | in-del | -/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109031798 | GGTCTCAAAAGTAGT[-/C]CACTCATAGAAACAG | 84749 |
rs34843806 | in-del | -/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109078737 | CCTAAAAACTTCCTT[-/C]TTAACATTTGTTATA | 84749 |
rs34912977 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | USP30 | GRCh38.p7 | 12:109081319 | TTTCTGGATTTTCTG[C/T]AATATTTCTTTCAGA | 84749 |
rs34994884 | in-del | -/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109076351 | GTGTATGCAAACAGT[-/G]CATGTTGCTTATGAA | 84749 |
rs34999664 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109081045 | ATGTTGATGAATATT[-/T]CTTGTAGTTATGCCC | 84749 |
rs35000756 | in-del | -/A | | | intron-variant | USP30 | GRCh38.p7 | 12:109080811 | GTGTTACAGTTGCTT[-/A]ACAGCATTCAGTACG | 84749 |
rs35058650 | in-del | -/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109033159 | TTTGAAACTTAAGTT[-/G]GGAGTGTCAGAGTCA | 84749 |
rs35062182 | in-del | -/A | | | intron-variant | USP30 | GRCh38.p7 | 12:109031225 | AATGGCATATTACAT[-/A]AAAACAACAACCCAT | 84749 |
rs35081175 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109029489 | TCCCCTGAGTGTGCA[-/T]TTTAGCTTCCCTATC | 84749 |
rs35164265 | in-del | -/A | | | intron-variant | USP30 | GRCh38.p7 | 12:109078423 | GTGAGACTGAGTCTC[-/A]AAAAAAAAAAAAAAA | 84749 |
rs35169304 | in-del | -/T | 0.494609 | 0.0516363 | intron-variant, upstream-variant-2KB, downstream-variant-500B | USP30, USP30-AS1 | GRCh38.p7 | 12:109051572 | ATCGCACCTGACCTC[-/T]TTTTTTTTTTTTTTT | 84749 |
rs35180726 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | USP30 | GRCh38.p7 | 12:109067254 | GAGTACCTGGGACTA[C/T]AGGCACCCACCACCA | 84749 |
rs35248521 | in-del | -/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109061316 | AGTGCTGGGAGCCAG[-/C]AGCCATCCTTGGGCT | 84749 |
rs35396504 | in-del | -/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109029714 | GCATGAGGTTAGAAA[-/G]GGGACCTGGAACAAA | 84749 |
rs35409409 | snp | A/G | 0.031825 | 0.122064 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109050720 | ACCAAAAAACAAAAA[A/G]ATAATGGGCCGGGCG | 84749 |
rs35466141 | in-del | -/A/AA | | | intron-variant | USP30 | GRCh38.p7 | 12:109066266 | AAAAAAAAAAAAAAA[-/A/AA]GCAAGCCTAAGATGT | 84749 |
rs35670961 | in-del | -/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109072493 | AGGAACTTGTATTTT[-/G]GGAAATAGCTTTAAA | 84749 |
rs35728674 | in-del | -/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109072361 | AGAGGTAGCTGTTTT[-/C]CCATTGAAATATAAC | 84749 |
rs35770985 | in-del | -/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109078905 | AAATTCATCACTTTA[-/G]AGGACATTGTTCTAT | 84749 |
rs35793725 | in-del | -/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109025755 | AGCTCACTGCAGCCT[-/G]GGACAGTAATCCTCC | 84749 |
rs35837643 | in-del | -/T | 0.492386 | 0.0612297 | intron-variant | USP30 | GRCh38.p7 | 12:109067281 | ACCACGCCCGGCTAA[-/T]TTTTTTTTTTTATTT | 84749 |
rs35927951 | in-del | -/T | | | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022794 | TAAACAAATCTAATG[-/T]TTGGGAAAACCAATT | 84749 |
rs35976007 | in-del | -/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109057215 | TTTTTTTTTAATGCT[-/C]CCCTTTTGAAAGTGT | 84749 |
rs35992495 | in-del | -/A | | | intron-variant | USP30 | GRCh38.p7 | 12:109038556 | TGAATGCTATTTATT[-/A]AAAATACTTACCTGC | 84749 |
rs36012313 | in-del | -/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109043964 | AAACATAGGTAGCAA[-/C]CCCGTGTCCATCAAC | 84749 |
rs36033006 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109079378 | TTTTTTTTTTTTTTT[A/T]TGTGACAGGGGTCTT | 84749 |
rs36085562 | in-del | -/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109041391 | CATGTAATCCCAGCA[-/C]TTTGGGAGGCTGAGG | 84749 |
rs36097563 | in-del | -/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109038742 | TGCTAGCAACGTATG[-/C]ATATCCAGTTGCTCC | 84749 |
rs55676204 | snp | C/T | 0.116838 | 0.211584 | intron-variant | USP30 | GRCh38.p7 | 12:109075008 | TCACATAGCAGATGT[C/T]CTCCAGGTTCATCCA | 84749 |
rs55741498 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | USP30 | GRCh38.p7 | 12:109071052 | ACACTGTATGATTCC[A/G]CTTGTGTGAGGTTCC | 84749 |
rs55795364 | snp | C/T | 0.125182 | 0.216612 | intron-variant | USP30 | GRCh38.p7 | 12:109049919 | AATGGTGCCAATAGA[C/T]TTGCTGTAGTCAGGT | 84749 |
rs56010602 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | USP30 | GRCh38.p7 | 12:109076172 | GCATTATTTTGATAC[C/T]ATTGTAAGTGGAATT | 84749 |
rs56212180 | snp | C/G | 0.11963 | 0.213316 | intron-variant | USP30 | GRCh38.p7 | 12:109056994 | TATTTCAGCCCCTCT[C/G]CAGACTGGAGTTGGA | 84749 |
rs56225739 | snp | C/T | 0.161596 | 0.233848 | intron-variant | USP30 | GRCh38.p7 | 12:109030677 | GCTGGAGTGCAGTGG[C/T]GCTATCTTGGCTCAC | 84749 |
rs56233132 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109079434 | AATAATGTGATCATA[A/G]CTCACTGCAGCCTCA | 84749 |
rs56405228 | in-del | -/T | 0.495927 | 0.0449436 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046418 | GCACCCAGCCCAGTC[-/T]TTTTTTTTTTTTCTT | 84749 |
rs56408293 | in-del | -/T | 0 | 0 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046120 | TTTTTTTTTTTTTTT[-/T]AGATGGAGTCTCACT | 84749 |
rs57059962 | snp | A/T | 0.172028 | 0.23753 | intron-variant | USP30 | GRCh38.p7 | 12:109041664 | AAAAGAAAAAGAAAA[A/T]GAATATATGTGAAGT | 84749 |
rs57270629 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109025518 | GAAAAATAGATGGTA[A/T]TGGGAAAAACTAAAT | 84749 |
rs57441878 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109079395 | GTGACAGGGGTCTTA[A/G]CTCTGTCACCGAGGC | 84749 |
rs57523881 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109059693 | AATGTTTGTATTTTT[-/T]AGTAGAGACAGTGTT | 84749 |
rs57753389 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | USP30 | GRCh38.p7 | 12:109029209 | TAGCTCTGGACCTGC[A/G]GTCAGTGTAAGAATT | 84749 |
rs57949633 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109075858 | TTTTTTTTTTTTTTT[-/T]GCTGTTGGTCCATAT | 84749 |
rs58002320 | snp | A/G | 0.0729998 | 0.176553 | intron-variant | USP30 | GRCh38.p7 | 12:109064979 | AGGGCTAGCCCCAGG[A/G]TATATACACACTGAT | 84749 |
rs58183883 | snp | C/T | 0.295088 | 0.245901 | intron-variant, upstream-variant-2KB, downstream-variant-500B | USP30, USP30-AS1 | GRCh38.p7 | 12:109051801 | TCTCGAACTCTTGAC[C/T]TCAGGTGATCCACCA | 84749 |
rs58263151 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | USP30 | GRCh38.p7 | 12:109028623 | GCTGAGATTACAGGC[A/G]TGTGCCAACACGCCT | 84749 |
rs58287875 | snp | C/G | 0.0310518 | 0.120672 | intron-variant | USP30 | GRCh38.p7 | 12:109048982 | TAAGGAGGCATGTCT[C/G]ACCTCTCATCTCATT | 84749 |
rs58578726 | in-del | -/TT | | | intron-variant | USP30 | GRCh38.p7 | 12:109026480 | GAATTTTTTTTTTTT[-/TT]GAGACAGGGTCTCTG | 84749 |
rs58730775 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109045581 | GTATGACCTTGGCCA[A/G]GTCAATTCACTTCTC | 84749 |
rs58828179 | snp | C/T | 0 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109023503 | GAGGTTGCAATGAGC[C/T]GAGATCGCGCCACTG | 84749 |
rs59129466 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109050730 | AAAAAAATAATGGGC[C/T]GGGCGCGGTGGCTCA | 84749 |
rs59162254 | snp | A/G | 0.135137 | 0.22205 | intron-variant, missense | USP30 | GRCh38.p7 | 12:109083071 | ACACCAGGTGTGTGC[A/G]CGCGAGGAGCCGATG | 84749 |
rs59198049 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109028461 | ACACCCTTTTTTTTT[-/T]CTGTTTTTTTGTTGT | 84749 |
rs59621777 | in-del | -/T | 0 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109067292 | CTAATTTTTTTTTTT[-/T]ATTTTTAGTGGAGAC | 84749 |
rs59806291 | in-del | -/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109079351 | TTTCTTTTTTTTTTT[-/C]TTTTTTTTTTTTTTT | 84749 |
rs59890684 | snp | G/T | 0.030278 | 0.119257 | intron-variant | USP30 | GRCh38.p7 | 12:109040619 | GTCTCATCTGAAGAC[G/T]TGACTGGGGCTGGAG | 84749 |
rs60060076 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | USP30 | GRCh38.p7 | 12:109049365 | GAAGAGTGAGAGAGA[C/G]GGGGGAACAGCCAGT | 84749 |
rs60197959 | in-del | -/A/AAA | 0 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109048753 | CAAAAAAAAAAAAAA[-/A/AAA]CAAAAAAAGAAAGAA | 84749 |
rs60618572 | in-del | -/T | 0.14933 | 0.228835 | intron-variant | USP30 | GRCh38.p7 | 12:109076411 | CCCAATCTTTATTCC[-/T]TTTTTTTTTTTTTCT | 84749 |
rs61062424 | in-del | -/A | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055401 | TATATATATATATAT[-/A]TTTTTTTTTTTTTTT | 84749 |
rs61083037 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | USP30 | GRCh38.p7 | 12:109056317 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 84749 |
rs61164773 | in-del | -/CA | | | intron-variant | USP30 | GRCh38.p7 | 12:109081624 | ACGCACGCATGCGCG[-/CA]CACACACACACACAC | 84749 |
rs61550352 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP30 | GRCh38.p7 | 12:109078196 | TTTGGAAGGCTGAGA[C/T]GAGTGGATCACGAGG | 84749 |
rs61588766 | in-del | -/AATA | | | intron-variant | USP30 | GRCh38.p7 | 12:109023554 | ATAAATAAATAAATA[-/AATA]GCCCCCTTATCATCC | 84749 |
rs61760225 | snp | C/T | 0.00130064 | 0.0254681 | synonymous-codon | USP30 | GRCh38.p7 | 12:109085808 | GTGGCTGTGGGTCTC[C/T]GATGACACTGTCCGC | 84749 |
rs61935536 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046212 | GTTTAAGTGATTCCC[A/C]TGCCTCAGCCTCCCT | 84749 |
rs61935537 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109048735 | ACAGAGTGAGACTCT[C/G]TCTCAAAAAAAAAAA | 84749 |
rs61935538 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055814 | AACAAACCCAGTGCA[A/T]TAAAAAAAAAAAAAA | 84749 |
rs61935539 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | USP30 | GRCh38.p7 | 12:109063056 | GTTCATCCATGTTAT[A/G]CCATGTATCAGAATT | 84749 |
rs61935540 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109071899 | ATTAGGGATGTCAAG[C/G/T]CTCTTTCAAATGATT | 84749 |
rs61935541 | snp | A/G | 0.260227 | 0.249791 | intron-variant | USP30 | GRCh38.p7 | 12:109072961 | ATAAGAAGCACAGCC[A/G]GAGCTGATCCCTGGG | 84749 |
rs71079513 | in-del | -/A | | | intron-variant | USP30 | GRCh38.p7 | 12:109032100 | GAGTGAGACTCTGTC[-/A]AAAAAAAAAAAAACA | 84749 |
rs71079514 | in-del | -/C | 0 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109035664 | ACCACACCCAGCCAC[-/C]ATTTTGATTTATAAC | 84749 |
rs71079515 | in-del | -/T | 0 | 0 | intron-variant, upstream-variant-2KB, downstream-variant-500B | USP30, USP30-AS1 | GRCh38.p7 | 12:109051587 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTGGT | 84749 |
rs71079516 | in-del | -/CGGCGG | 0 | 0 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052639 | CGGCGGCGGCGGCGG[-/CGGCGG]TAGCGGAGGAGACGG | 84749 |
rs71079520 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109076733 | TGATTGATTTTTTCT[-/T]TTTTTTTTTTTTTTT | 84749 |
rs71079521 | in-del | -/TTT | | | intron-variant | USP30 | GRCh38.p7 | 12:109079352 | TTCTTTTTTTTTTTC[-/TTT]TTTTTTTTTTTTTTT | 84749 |
rs71443827 | in-del | -/T | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109038148 | ATTCATGAGCTGTTA[-/T]TTCTGATGCTCTCCC | 84749 |
rs71443828 | in-del | -/T | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109038151 | ATGAGCTGTTATTTC[-/T]TGATGCTCTCCCTCC | 84749 |
rs71443829 | in-del | -/G | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109039658 | CCCTGTCACCAGGCT[-/G]GTAGTTCAGTGGCAC | 84749 |
rs71443830 | in-del | -/ATATATATACATATATATATATATACATATATATATATATACATATATAT | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055369 | TATATACACACACAC[lengthTooLong]ATATATATACATATA | 84749 |
rs71443831 | in-del | -/ATAT | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055380 | CACACATATATATAC[-/ATAT]ATATATATATATATA | 84749 |
rs71443832 | in-del | -/T | 0.49645 | 0.0419827 | intron-variant | USP30 | GRCh38.p7 | 12:109063107 | ATAATATTCTTTCTA[-/T]TTTTTTTTTTAAGAC | 84749 |
rs71443833 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109075842 | TCATGTTACTTTTTC[-/T]TTTTTTTTTTTTTTT | 84749 |
rs71445284 | in-del | CTT/TC | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109079354 | TTTTCTTTTTTTTTT[CTT/TC]TTTTTTTTTTTTTTT | 84749 |
rs71454762 | snp | A/G | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109056103 | GTGGAGTGAGAGGCA[A/G]AAAAGGAAAATAACT | 84749 |
rs71454763 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | USP30 | GRCh38.p7 | 12:109063933 | GCTGGATTGCAGTGG[C/T]GCCATCTCAGCTCAC | 84749 |
rs71454764 | snp | A/G | 0.031825 | 0.122064 | intron-variant | USP30 | GRCh38.p7 | 12:109072673 | TTCCAGTGCTGCCAA[A/G]TTCTATTGCATATTA | 84749 |
rs73195455 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | USP30 | GRCh38.p7 | 12:109063560 | TTATTTTCTGTAAAC[A/C]CTCAGAAGTAGAATT | 84749 |
rs73195456 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109063878 | TTTTGAATTGGGTTT[C/T]TTTTTTTTTTTTTTT | 84749 |
rs73195457 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | USP30 | GRCh38.p7 | 12:109067420 | CCACACCCAGCCTGC[G/T]GTCTTTAATTTTTAA | 84749 |
rs73195460 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109082335 | GCTACCTGCCTGACT[A/C]CCCTAAGTAACTTGA | 84749 |
rs73413033 | snp | C/T | 0.242775 | 0.249896 | upstream-variant-2KB, utr-variant-5-prime | USP30, SVOP | GRCh38.p7 | 12:109021160 | AGTTCACAGGCTCTC[C/T]GGCTGATGGTGTATC | 84749 |
rs73413034 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | USP30 | GRCh38.p7 | 12:109027592 | CCTATTCTACTTCCT[A/G]TTTCTATGAATTTGC | 84749 |
rs73413037 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | USP30 | GRCh38.p7 | 12:109030372 | TTGTATGAAACAAAT[A/G]TATGTCAAACTCCCA | 84749 |
rs73413039 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109030740 | TCTGCCTAAGTCCCC[C/T]GACTAACTGGGATTA | 84749 |
rs73413041 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | USP30 | GRCh38.p7 | 12:109031063 | TCCTGTAAATCCAAA[A/G]TTATTCCAAAATAAA | 84749 |
rs73413043 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | USP30 | GRCh38.p7 | 12:109033522 | TAGCCTTGGAGCAAT[A/G]CTATGTGCCCTGAGT | 84749 |
rs73413044 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | USP30 | GRCh38.p7 | 12:109033617 | TGATCAAATTTCACA[C/T]GATTTAAAGAAAAAA | 84749 |
rs73413046 | snp | C/T | 0.0622301 | 0.165053 | intron-variant | USP30 | GRCh38.p7 | 12:109034019 | GTGTTCCCAGAGGGC[C/T]GTAACATAAACAAGG | 84749 |
rs73413051 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | USP30 | GRCh38.p7 | 12:109035676 | CACCATTTTGATTTA[C/T]AACAATCTAGTTTGG | 84749 |
rs73413064 | snp | A/G | 0.0618563 | 0.164627 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054194 | ACTCACGTATCGTGT[A/G]AAAGCACAGTGATGT | 84749 |
rs73413072 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | USP30 | GRCh38.p7 | 12:109063049 | CTTCAGGGTTCATCC[A/G]TGTTATACCATGTAT | 84749 |
rs73413074 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | USP30 | GRCh38.p7 | 12:109070643 | AGTGTGAGGGGACAC[C/T]AAAGGAGAAGCAGAG | 84749 |
rs74236973 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109034705 | TTGTTCTATCCATTA[C/T]TGAAAGTAGGATATA | 84749 |
rs74346881 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | USP30 | GRCh38.p7 | 12:109080136 | ACGTGTGGTTCAGGG[A/T]TCAGCCCTGGAATTG | 84749 |
rs74397199 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | USP30 | GRCh38.p7 | 12:109063825 | GGCCATTTTGTCTAT[C/G]TTTTTGGGAGAAATG | 84749 |
rs74456627 | snp | A/T | 0.029116 | 0.117091 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109086347 | TTGTTGACAAGAATT[A/T]ATGAAATTATTAAAG | 84749 |
rs74521706 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109051222 | GGGTCAAGGAAAAAA[A/T]ATGGTTAAAATTAAT | 84749 |
rs74548103 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | USP30 | GRCh38.p7 | 12:109056145 | TCAGAGTGAGAAGTA[A/G]CCTTTGGAATGTGAT | 84749 |
rs74560693 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | USP30 | GRCh38.p7 | 12:109079489 | CCACCTTAGCCCCCT[A/G]AGCAGCTGGGACTAC | 84749 |
rs74690825 | snp | C/T | 0.029116 | 0.117091 | intron-variant | USP30 | GRCh38.p7 | 12:109084088 | AGCAGTAGGGCCACT[C/T]GTGGTGGCTCACACC | 84749 |
rs74701456 | snp | G/T | 0 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109036487 | ATTTTGGATAGAGAT[G/T]GGGTTTCACCATGTT | 84749 |
rs74836577 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109059007 | AGTACTGTTTGACCC[A/G]GTAATTCCATGTCTG | 84749 |
rs74870168 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053519 | CAGAACTGAGTACCC[A/C]CTCCCCCACTGCTGA | 84749 |
rs74891503 | snp | A/C/T | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109037956 | AGATACTCAGAATTA[A/C/T]ATCTGAATTTTTCAA | 84749 |
rs74908026 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | USP30 | GRCh38.p7 | 12:109070501 | GCCAGGGGCCGGGAC[A/T]TTGTGAATGTTGGGG | 84749 |
rs74942489 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP30 | GRCh38.p7 | 12:109072964 | AGAAGCACAGCCAGA[A/G]CTGATCCCTGGGCTG | 84749 |
rs74979708 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | USP30 | GRCh38.p7 | 12:109040239 | TTTAGAGTTTAACTA[C/T]TAAGGAAGTGATTAG | 84749 |
rs74998271 | snp | A/T | 0 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109039619 | AGTGATAAGAATCCA[A/T]TTTTTTTTTTGAGAT | 84749 |
rs75008404 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | USP30 | GRCh38.p7 | 12:109041549 | CTGAGGCAGAGGAAT[C/T]GCTTGAACCTGGTAG | 84749 |
rs75107806 | snp | A/G | 0.200182 | 0.244986 | intron-variant | USP30 | GRCh38.p7 | 12:109070331 | GTGGGTTAGAGTTCA[A/G]AGGGGTGGAGGCAGC | 84749 |
rs75135844 | snp | C/T | 0.126219 | 0.217206 | intron-variant | USP30 | GRCh38.p7 | 12:109057104 | AGTGGTACAGACTGA[C/T]CAATTACATCATACA | 84749 |
rs75223116 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109063359 | GCCCACCTCAGCCTC[C/T]CAAAGTTCTGGGATT | 84749 |
rs75223328 | in-del | -/AATT | | | intron-variant | USP30 | GRCh38.p7 | 12:109061409 | AAAAAAAAAAAAAAA[-/AATT]TTTTTTTTTTTTTAG | 84749 |
rs75231104 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109051249 | TAATTTTACCTCTTG[C/T]TTTTTTTTTTTTTTT | 84749 |
rs75382896 | snp | A/G | 0.00109094 | 0.0233299 | missense | USP30 | GRCh38.p7 | 12:109072342 | AACAAATTACCTGCC[A/G]CACAAGAGGTAGCTG | 84749 |
rs75436767 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109041788 | TTGGAAGGTCGAACT[A/G]TGAGTTTACTATTGT | 84749 |
rs75505358 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | USP30 | GRCh38.p7 | 12:109049658 | CATCTCTACTAAAAA[C/T]GCTAAAATTAGCCAG | 84749 |
rs75539714 | snp | A/C | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109071044 | AAAGACCAACACTGT[A/C]TGATTCCACTTGTGT | 84749 |
rs75653395 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | USP30 | GRCh38.p7 | 12:109048151 | AGTGCAGTGGCACAA[C/T]CATGGCTCACTGCAA | 84749 |
rs75680871 | snp | A/G | 0.118933 | 0.212888 | intron-variant | USP30 | GRCh38.p7 | 12:109061464 | CCCAGGCTGGAGTGC[A/G]GTGGCACAACCTCAG | 84749 |
rs75751817 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | USP30 | GRCh38.p7 | 12:109050528 | CAGGTATGCGACACC[A/T]CCCCCAGCATGAATG | 84749 |
rs75774029 | snp | C/G/T | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109070324 | GCTGAGGGTGGGTTA[C/G/T]AGTTCAGAGGGGTGG | 84749 |
rs75876283 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109073942 | TTATTTTATTTTTTC[A/C]CAGCCATTACTGACT | 84749 |
rs75961872 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109031634 | ATGGATAAACAAAAT[A/G]TGGTCTATCCATGCA | 84749 |
rs76006031 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055843 | AAGAAAAGAAAAAAA[A/C]CATAGCGAATAGGTT | 84749 |
rs76009193 | snp | A/G/T | 0.0215923 | 0.101639 | intron-variant | USP30 | GRCh38.p7 | 12:109067510 | AATAATTGTCTTACC[A/G/T]TTTTTGTTTCCAGCC | 84749 |
rs76055259 | snp | A/T | 0 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109057190 | CTTCATTACTAAAAA[A/T]TTATTTTCTTTTTTT | 84749 |
rs76112868 | snp | A/G | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109060319 | TTTTGGAAAAAAACT[A/G]TACTTCAACTTTTAA | 84749 |
rs76113917 | snp | A/G | 0.193028 | 0.243422 | intron-variant | USP30 | GRCh38.p7 | 12:109025778 | AATCCTCCTGCCTCA[A/G]CCCAGCTCTAGCGAT | 84749 |
rs76155358 | snp | A/C | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109041634 | AGCGAAACTCCATTT[A/C]AAAAAAAAAAAGAAA | 84749 |
rs76231306 | snp | A/C | 0.00517822 | 0.0506191 | utr-variant-5-prime, upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109023091 | AACACTTGTCAGTAT[A/C]CCCATTGTTGCATAG | 84749 |
rs76325933 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109075841 | ATCATGTTACTTTTT[C/T]TTTTTTTTTTTTTTT | 84749 |
rs76359179 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109063117 | TTCTATTTTTTTTTT[A/T]AAGACAAAGTCTCAT | 84749 |
rs76360645 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP30 | GRCh38.p7 | 12:109082209 | AGATGAGTTTTGTTT[C/T]ATGCACAGTGTTTAA | 84749 |
rs76467581 | snp | A/C | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109058574 | CGAAACTCCGTCTCA[A/C]AAAAAAAAAAAAATC | 84749 |
rs76544948 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | USP30 | GRCh38.p7 | 12:109081568 | AGAGGAAAATGAATC[A/G]TTTTTCTTTTGCTCC | 84749 |
rs76626923 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109059921 | ATGCACAAAGATCTC[C/T]AACACCTAATTATAA | 84749 |
rs76644944 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP30 | GRCh38.p7 | 12:109037173 | TCATGTTCATTGATA[C/T]TTTGCTTACCTGTTC | 84749 |
rs76756235 | snp | C/T | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109036308 | GTATTTCTTTCTTTC[C/T]TTTTTTTTTTTTTAG | 84749 |
rs76779951 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109087854 | CATTAAGTAGCAGCC[C/T]AATAATCTGATTTCT | 84749 |
rs76792547 | snp | A/T | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109057211 | TTCTTTTTTTTTTTA[A/T]TGCTCCCTTTTGAAA | 84749 |
rs76866293 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | USP30 | GRCh38.p7 | 12:109079899 | TGTATTTTATGTTTG[A/G]TAATTTTTTATTGTA | 84749 |
rs76940465 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | USP30 | GRCh38.p7 | 12:109038069 | TGCAGGTTTGTTACA[C/T]AGGTAAGTGTGCCAT | 84749 |
rs76988801 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | USP30 | GRCh38.p7 | 12:109066665 | ACTCCACCCTGGGCG[A/G]CAGAGCACGACTCTG | 84749 |
rs77003385 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109047132 | AACCACCTTTTACTC[C/T]TCCAACGGGTTTAGT | 84749 |
rs77072131 | snp | A/C | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109032101 | AGTGAGACTCTGTCA[A/C]AAAAAAAAAAAACAC | 84749 |
rs77101495 | snp | A/T | 0 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109078437 | TCAAAAAAAAAAAAA[A/T]ATAGCTGCACCAGTT | 84749 |
rs77203415 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | USP30 | GRCh38.p7 | 12:109029923 | TCTGAGAAAGTTCCC[C/T]GAGTTCTCCAGCCCT | 84749 |
rs77241135 | snp | A/C/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109047399 | ACAGTTCTGACATGC[A/C/T]GTGTGAGGTGGAATT | 84749 |
rs77269577 | snp | C/T | 0.00953873 | 0.0683987 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109021604 | CTTCAAGATCCTAGA[C/T]AGTTTAATGGTTCCC | 84749 |
rs77292330 | snp | A/C | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109078600 | CGAGACTCCATCTCA[A/C]AAAAAAAAAAAAGAG | 84749 |
rs77295439 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | USP30 | GRCh38.p7 | 12:109071330 | TGAAATCGGAGTGGA[G/T]GTCAAGGCTGTCTCA | 84749 |
rs77359530 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109051221 | TGGGTCAAGGAAAAA[A/T]TATGGTTAAAATTAA | 84749 |
rs77428001 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | USP30 | GRCh38.p7 | 12:109044891 | CATCATTATGTTATC[A/C]CACTTTTTCATGCTT | 84749 |
rs77476513 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | USP30 | GRCh38.p7 | 12:109057739 | TGTGCTTACAGTCTG[C/T]GGAGCAGTACTAGAA | 84749 |
rs77515951 | snp | G/T | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109059848 | TTTGACTGTAGAACT[G/T]TTTTTTTTCTTCATA | 84749 |
rs77517679 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | USP30 | GRCh38.p7 | 12:109034579 | TTAAAAAAGAAAGAA[A/T]GAGAGAAAATGCATT | 84749 |
rs77530307 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP30 | GRCh38.p7 | 12:109075327 | AGTTGCCTTCTCTCC[A/G]CACCCTCGGCAACAC | 84749 |
rs77638880 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109051251 | ATTTTACCTCTTGCT[C/T]TTTTTTTTTTTTTTT | 84749 |
rs77695145 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | USP30 | GRCh38.p7 | 12:109041326 | TCCTGAAAGCTTGCT[A/G]GGGCTTCATGATTTA | 84749 |
rs77767632 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | USP30 | GRCh38.p7 | 12:109038516 | TATCTTTTTTTTGCT[A/G]CAATTGTTATTCATT | 84749 |
rs77881178 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109051275 | TTTTTTTTTTTTTTT[A/G]ATGCTGAATCTCTCT | 84749 |
rs78010052 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053915 | GCACAGACCTGGGGA[A/G]ACAGACAGGCATGAT | 84749 |
rs78021343 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | USP30 | GRCh38.p7 | 12:109069197 | CTCCTCTGCAGTGCT[G/T]TCCCTTTCCTTAAGG | 84749 |
rs78073059 | snp | A/T | 0.116838 | 0.211584 | intron-variant | USP30 | GRCh38.p7 | 12:109084879 | GGGGAGTTAACTTTC[A/T]AGGTAATCAAAACCA | 84749 |
rs78082461 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | USP30 | GRCh38.p7 | 12:109042635 | TTAAAAACAATGTTA[C/T]AGAACATTATACTCA | 84749 |
rs78176681 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109061603 | TGAGTAGAGACAGGG[G/T]TTTGACTTGTTGCCC | 84749 |
rs78202968 | snp | A/G | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109068227 | GAAGTTCTAGAGATG[A/G]AAAAATCTAGCCCCC | 84749 |
rs78219302 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109047170 | ACAGAGGTGGATGCA[A/T]TTTTTTTTTTTAACC | 84749 |
rs78418722 | in-del | -/TTT | | | intron-variant | USP30 | GRCh38.p7 | 12:109076422 | TTCCTTTTTTTTTTT[-/TTT]CTTTGCCTTATTATC | 84749 |
rs78490017 | snp | A/C | 0 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109066250 | GAGACCCTGTCTCAA[A/C]AAAAAAAAAAAAAAA | 84749 |
rs78607011 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109030550 | TAGGTAACGATACTT[G/T]AAATTTCTTAAAAGG | 84749 |
rs78608917 | snp | A/C | 0.20111 | 0.245173 | intron-variant | USP30 | GRCh38.p7 | 12:109047872 | TTAGTATTCACCCAG[A/C]CAGCTAAAGTGGTGG | 84749 |
rs78753245 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | USP30 | GRCh38.p7 | 12:109062824 | TCTCTAGAACTCTTC[A/G]TCATCCCGTACTGAA | 84749 |
rs78785138 | snp | A/G | 0.15665 | 0.231917 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022190 | GCTCCCCAGCACCAT[A/G]AAGTGGAAACCCCTG | 84749 |
rs78849584 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109063354 | GATCTGCCCACCTCA[A/G]CCTCCCAAAGTTCTG | 84749 |
rs78864002 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | USP30 | GRCh38.p7 | 12:109083860 | CACAGTTGCATGGCC[C/T]GACACCTCATCATGT | 84749 |
rs78884214 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055784 | CAAAGCACATGCCAG[C/T]TGAGGGAGACAGACA | 84749 |
rs78885554 | snp | C/T | 0.0231231 | 0.105009 | synonymous-codon | USP30 | GRCh38.p7 | 12:109081384 | ACTAAGTATTCCAGC[C/T]GCCACATGGGTATGT | 84749 |
rs78909524 | snp | A/G | 0.00121833 | 0.0246512 | missense | USP30 | GRCh38.p7 | 12:109085789 | CTCTCTCAACTAGCA[A/G]TCAGTGGCTGTGGGT | 84749 |
rs78982330 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | USP30 | GRCh38.p7 | 12:109072813 | CTGTTTGCCAGGCAT[C/T]GCATTATCTCATTTA | 84749 |
rs79010121 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | USP30 | GRCh38.p7 | 12:109078919 | TAAGGACATTGTTCT[A/G]TTGTCTTCTGGCCTC | 84749 |
rs79015774 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046092 | TTGGGGGAAGTCAGT[C/T]TTTTTTTTTTTTTTT | 84749 |
rs79071652 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109061604 | GAGTAGAGACAGGGT[A/T]TTGACTTGTTGCCCA | 84749 |
rs79080481 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046418 | GCACCCAGCCCAGTC[C/T]TTTTTTTTTTTTCTT | 84749 |
rs79179032 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109065791 | AAGCAGTGGCCATGC[G/T]CCAGAGAAGAAAAGC | 84749 |
rs79237141 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054384 | AAAATTACCTGGGCA[C/T]GTGGTGTGCAGCTGT | 84749 |
rs79303986 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | USP30 | GRCh38.p7 | 12:109031209 | TGACTACACGCATTG[A/G]AAATGGCATATTACA | 84749 |
rs79312401 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | USP30 | GRCh38.p7 | 12:109025979 | TGTGAGCCACTGACC[C/T]TGGCATGAAGCGTTT | 84749 |
rs79518645 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046417 | TGCACCCAGCCCAGT[C/T]TTTTTTTTTTTTTCT | 84749 |
rs79538094 | snp | A/C | 0.0573587 | 0.15934 | intron-variant | USP30 | GRCh38.p7 | 12:109032768 | ATATACTTTAAAAAA[A/C]CCCTATTAAATTGCA | 84749 |
rs79631510 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | USP30 | GRCh38.p7 | 12:109074910 | GGCAGCCAGCATGTA[C/G]TCTGCTTCTGTGAGT | 84749 |
rs79654305 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109050990 | GCAAGACTCCATCTC[A/C]AAAAAAAAAGAATGT | 84749 |
rs79751199 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055816 | CAAACCCAGTGCATT[A/T]AAAAAAAAAAAAAGA | 84749 |
rs79777919 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | USP30 | GRCh38.p7 | 12:109026813 | TGACAAGTTCAAGAT[C/G]AAAGTGCCAGTATAG | 84749 |
rs79820769 | snp | C/T | 0.202035 | 0.245356 | intron-variant | USP30 | GRCh38.p7 | 12:109081672 | ACACACAGACATTAA[C/T]CTCAGATTGAAAGAT | 84749 |
rs79932573 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109057209 | TTTTCTTTTTTTTTT[A/T]AATGCTCCCTTTTGA | 84749 |
rs79998109 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | USP30 | GRCh38.p7 | 12:109070443 | GGTCTGAGCACAGCC[C/T]GAAATGGGAATAAGC | 84749 |
rs80001507 | snp | G/T | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109048094 | TTTTTTTTTTTTTTT[G/T]TTGAGACATGGTCTT | 84749 |
rs80022791 | snp | A/C | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109058572 | AGCGAAACTCCGTCT[A/C]AAAAAAAAAAAAAAA | 84749 |
rs80060613 | snp | A/T | 0 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109032154 | TCTACAAAAAAAAAA[A/T]TTACCTGGGCATGGT | 84749 |
rs80131322 | snp | C/T | 0 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109023850 | GTCAGGAGTTCAAGA[C/T]CAGCCTGGCCAACGT | 84749 |
rs80212555 | snp | A/G | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109059417 | GCCAGGCTAGTCTCA[A/G]ACTCCTGGCCTCAAG | 84749 |
rs80241678 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP30 | GRCh38.p7 | 12:109065390 | TCCATTTGTTTAGGT[A/G]CTGCCTATGTCAGCC | 84749 |
rs80321363 | snp | C/T | 0.123105 | 0.215401 | utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109024877 | ACCTGCCTTGGCCCC[C/T]CAAAGTGCTGGGATT | 84749 |
rs80335204 | snp | A/C | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109078598 | AGCGAGACTCCATCT[A/C]AAAAAAAAAAAAAAG | 84749 |
rs111228397 | in-del | -/TTGT | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109030615 | AAAAAGGTAGGTTGC[-/TTGT]TTGTTTGTTTGTTTT | 84749 |
rs111329986 | in-del | -/A | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109072407 | TTTTAAGATATGATA[-/A]TAATTTGCTTGTTTT | 84749 |
rs111398693 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | USP30 | GRCh38.p7 | 12:109081621 | CACACGCACGCATGC[A/G]CGCACACACACACAC | 84749 |
rs111501176 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | USP30 | GRCh38.p7 | 12:109059016 | TGACCCAGTAATTCC[A/G]TGTCTGGGAGTCCGC | 84749 |
rs111502182 | snp | A/G | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109071386 | GCTGGCGTGAAGGCA[A/G]CCACCTGGCTTTCTC | 84749 |
rs111595918 | in-del | -/G | 0.181022 | 0.240296 | intron-variant | USP30 | GRCh38.p7 | 12:109045449 | AGTGGGGGTGGGGGG[-/G]TGATGGTCCCAGCCT | 84749 |
rs111643555 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | USP30 | GRCh38.p7 | 12:109027768 | CTTTGTAGGTATATG[A/G]CACATTTTGTTAATC | 84749 |
rs111675091 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109048520 | TCCGTATCTTGATTC[A/C]CCTGAGGTCAGGAGT | 84749 |
rs111682301 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | USP30 | GRCh38.p7 | 12:109083346 | TAATTTTTCCGCTAA[A/G]TGATATAATCATTGG | 84749 |
rs111720237 | snp | C/T | 0.128976 | 0.218754 | intron-variant | USP30 | GRCh38.p7 | 12:109044445 | GAGTTTGACACCAGC[C/T]TGGGCAACATAGTGA | 84749 |
rs111724123 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109021803 | TCCATTTCAAACCAA[C/T]TGAACTCAACTCTCG | 84749 |
rs111762860 | in-del | -/G/T/TT/TTT | 0.557685 | 0.146316 | intron-variant | USP30 | GRCh38.p7 | 12:109072281 | AAGGTTTTCAGTCTG[-/G/T/TT/TTT]TTTTTTTTTTTTCTC | 84749 |
rs111763356 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | USP30 | GRCh38.p7 | 12:109038967 | GAATTGTTTTTCTTC[G/T]TATTGAATTGCAAGA | 84749 |
rs111769280 | snp | A/C | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109048754 | CAAAAAAAAAAAAAA[A/C]AAAAAAAGAAAGAAA | 84749 |
rs111830509 | snp | C/T | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109068170 | TCCTCCCCGCCAGAC[C/T]GCTGTTACCAACAGC | 84749 |
rs111880265 | snp | A/C | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109080707 | TTTTGGTCAATGACA[A/C]ACCACATATATGATG | 84749 |
rs111937977 | snp | A/G | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109084453 | GTTTTGCCTCCCAAG[A/G]GACATTGGGCAGTGT | 84749 |
rs111944941 | in-del | -/A/AA | 0.424814 | 0.178718 | intron-variant | USP30 | GRCh38.p7 | 12:109058572 | GCGAAACTCCGTCTC[-/A/AA]CAAAAAAAAAAAAAA | 84749 |
rs111982927 | snp | C/T | 0.281049 | 0.248064 | utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109024870 | GTGATCCACCTGCCT[C/T]GGCCCCCCAAAGTGC | 84749 |
rs112003965 | snp | C/T | 0.118933 | 0.212888 | intron-variant | USP30 | GRCh38.p7 | 12:109062192 | CACCCGCCTCAGCCT[C/T]CCGTAGTGCTGGGAT | 84749 |
rs112004104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109069814 | CCAGGTAGGGAGGCT[C/T]CTCTCAGGAGGTGAG | 84749 |
rs112086493 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046467 | TAATTGGATGAGGCC[C/T]ACCCACTATTTGGAG | 84749 |
rs112089935 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP30 | GRCh38.p7 | 12:109040729 | CATGGACCTCTCCAT[A/G]ATGCTGCCTGGGCAT | 84749 |
rs112171892 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109063152 | TCACCCAGGCTGGAG[C/T]GCAGTGGTGCGATCT | 84749 |
rs112211712 | in-del | -/T | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109039619 | AGTGATAAGAATCCA[-/T]TTTTTTTTTTGAGAT | 84749 |
rs112268167 | snp | A/C | 0.081446 | 0.184634 | intron-variant | USP30 | GRCh38.p7 | 12:109048519 | TTCCGTATCTTGATT[A/C]ACCTGAGGTCAGGAG | 84749 |
rs112357511 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109068026 | AAAAAATCAATCTTC[A/G]GAGCTTTGCTTAAAG | 84749 |
rs112406436 | in-del | -/A | 0.237014 | 0.249662 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | USP30, USP30-AS1 | GRCh38.p7 | 12:109054529 | GCAAGACACTGTCTC[-/A]CAAAAAAAAATAAAA | 84749 |
rs112525806 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053496 | ACCCTCCCAAGGGCT[C/T]CAGGCTTCAGAACTG | 84749 |
rs112536202 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP30 | GRCh38.p7 | 12:109032966 | GACTGACAAGCTGCC[C/T]CTTAGCCTGAAATAC | 84749 |
rs112560175 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | USP30 | GRCh38.p7 | 12:109081157 | TTATTGTACCTCTTA[C/T]GTGTACAAGGTTGTT | 84749 |
rs112623344 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109027468 | ATTTTTCTGTAGAGA[C/T]AGAGTCTTGCTATGT | 84749 |
rs112645060 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | USP30 | GRCh38.p7 | 12:109035433 | CAGTGGCACAATCTC[A/G]GCTTACTGCAACCTC | 84749 |
rs112659795 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | USP30 | GRCh38.p7 | 12:109026536 | ATGATCATGGCTCAC[G/T]GCAGCCTCAACCTCC | 84749 |
rs112696760 | snp | A/G | 0.0618563 | 0.164627 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109051369 | TCTAGCGATTCTCCC[A/G]CCTCAGCCTCCCGAG | 84749 |
rs112713423 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP30 | GRCh38.p7 | 12:109040625 | TCTGAAGACTTGACT[A/G]GGGCTGGAGGATCCA | 84749 |
rs112834282 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP30 | GRCh38.p7 | 12:109041096 | AACTGAGCTGGCCTC[C/T]GATAGTCTCTTCAGT | 84749 |
rs112834387 | snp | A/G | 0.119281 | 0.213102 | intron-variant | USP30 | GRCh38.p7 | 12:109066600 | TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG | 84749 |
rs112899702 | in-del | -/A | 0 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109036957 | TTTGATGTATAGATT[-/A]ATGTTTTCCATAAAA | 84749 |
rs112907632 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109063748 | CCTAATGGTATGGTA[A/G]TTGCTTTAATTTGCA | 84749 |
rs112931822 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046515 | AAAAGTCCACCAATT[C/T]AAATGTTAATCTCAT | 84749 |
rs112997894 | in-del | -/T | 0.0360663 | 0.129354 | intron-variant | USP30 | GRCh38.p7 | 12:109083834 | TTACTCCTTTTGTTC[-/T]TTTTTATGACCACAG | 84749 |
rs112998628 | snp | C/T | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109068162 | GGCCACCCTCCTCCC[C/T]GCCAGACCGCTGTTA | 84749 |
rs113063923 | snp | C/T | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109038827 | TGTGTGGTGGTATTA[C/T]ATAATGGTGTTAATT | 84749 |
rs113103091 | snp | A/G | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109069810 | TGCTCCAGGTAGGGA[A/G]GCTCCTCTCAGGAGG | 84749 |
rs113233599 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | USP30 | GRCh38.p7 | 12:109041622 | CCTGGGTGACAGAGC[A/G]AAACTCCATTTCAAA | 84749 |
rs113234729 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109063126 | TTTTTTTAAGACAAA[A/G]TCTCATTCTGTCACC | 84749 |
rs113399484 | snp | G/T | 0.0356815 | 0.128715 | intron-variant | USP30 | GRCh38.p7 | 12:109077828 | GTGTGTTTGTGTTGG[G/T]GGGGGAGGGTGTGTG | 84749 |
rs113456528 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109069918 | TGAAGAAGCTAGGGT[A/G]TAAGTCTGGAGATGG | 84749 |
rs113473989 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109067369 | TAATCTGCCCACTTC[A/G]GCCTCCCAAAATTCT | 84749 |
rs113484084 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109026929 | ATAAAGAGAAAGCAA[A/G]CTCTCTGGCATATTT | 84749 |
rs113536404 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109047126 | TAGTAAAACCACCTT[C/T]TACTCCTCCAACGGG | 84749 |
rs113546679 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | USP30 | GRCh38.p7 | 12:109071114 | ATGGTGGGTGCCAGG[A/G]GTTGGGGAAGGGGAA | 84749 |
rs113694239 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053057 | AAGGCCCCTAATTCT[A/G]TCAGTGCCCTCAGTC | 84749 |
rs113695426 | snp | A/G | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109083780 | GCCCCCAGTTAGGTC[A/G]GGATTGTCTCACACC | 84749 |
rs113780866 | in-del | -/A | 0 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109072026 | CTCATTTCCCTGTAA[-/A]CAGTATAAATATCGG | 84749 |
rs113804305 | snp | G/T | 0.0607341 | 0.163335 | intron-variant | USP30 | GRCh38.p7 | 12:109040192 | AAAAAAAAATTTAGG[G/T]TGCTACCAAAATACC | 84749 |
rs113907555 | snp | C/G | 0.5 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109080433 | AAACGGTTTTGTTTT[C/G]TTGCAAACTTTACAA | 84749 |
rs113909030 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109082079 | GCTGATGTAGCGCCT[C/T]TCACACCAGTGACCC | 84749 |
rs113927204 | in-del | -/ATG | 0.133777 | 0.221342 | intron-variant | USP30 | GRCh38.p7 | 12:109068496 | GGTCACTTTTTAGAC[-/ATG]GTGGTGGTATCTATA | 84749 |
rs113932805 | snp | A/G/T | 0.00398564 | 0.0444627 | intron-variant | USP30 | GRCh38.p7 | 12:109035642 | GCTGGGATTACAGGC[A/G/T]TGAGCCACCACACCC | 84749 |
rs113983781 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | USP30 | GRCh38.p7 | 12:109032295 | GGAGATAGAATGATA[C/G]TGTCTAAAAAACAAA | 84749 |
rs113984502 | snp | C/T | 0.021333 | 0.101051 | intron-variant | USP30 | GRCh38.p7 | 12:109024791 | CCCTGGGCTAATTTT[C/T]TGTATTTTTAGTATT | 84749 |
rs114000696 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP30 | GRCh38.p7 | 12:109033257 | GGCATACCCATAGAC[C/T]GGGTAGTCTTCAGTA | 84749 |
rs114044915 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP30 | GRCh38.p7 | 12:109064427 | GCACCCATCACCCCC[A/G]GCTAATTTTTGGGTG | 84749 |
rs114118250 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP30 | GRCh38.p7 | 12:109039910 | CACCACACCTGGCCA[A/G]CCATTTTCTTTCTTT | 84749 |
rs114163465 | snp | C/T | 0.00716266 | 0.059414 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109086185 | GAGTGTCTTTTTACT[C/T]ATCTGATACAGGTAA | 84749 |
rs114178663 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | USP30 | GRCh38.p7 | 12:109072901 | CCCAATTTTCCGCAC[A/T]CTGAGGCTTGTAGAG | 84749 |
rs114241024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109078714 | CATTTGATGTTTTTT[C/T]CCTTTTGGCCTAAAA | 84749 |
rs114305256 | snp | A/G | 0.0310518 | 0.120672 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053205 | GGTTCTTCTAGTCCT[A/G]TAAGTGCCCCGGGCC | 84749 |
rs114369177 | snp | A/G | 0.00159775 | 0.0282192 | synonymous-codon, missense, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088488 | ATCTCGGTGCTCCCC[A/G]ATGTGGTCACAGCCA | 84749 |
rs114432649 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | USP30 | GRCh38.p7 | 12:109079718 | CAACAAATTTTTCAT[A/C]GTAATCACTGTTGTT | 84749 |
rs114443624 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109044157 | TATGTGAGATACTTA[C/G]AGTAGTTGAATAAAT | 84749 |
rs114547561 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | USP30 | GRCh38.p7 | 12:109066819 | CAGCCCTGTGGAGAG[A/G]AGTGTAGCACCAAAT | 84749 |
rs114561389 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | USP30 | GRCh38.p7 | 12:109038756 | TGATATCCAGTTGCT[C/T]CAAATCCTCACCAAC | 84749 |
rs114617705 | snp | G/T | 0.108755 | 0.206276 | intron-variant | USP30 | GRCh38.p7 | 12:109024584 | TTTTAAGTATCAACT[G/T]GGTGGGTTTAAGGAA | 84749 |
rs114685744 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | USP30 | GRCh38.p7 | 12:109026046 | AAACCATGTGTATCT[C/T]ACTACCATGATTCTT | 84749 |
rs114748064 | snp | A/G | 0.0232847 | 0.105357 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053376 | GGTCAGGGCCCCTTT[A/G]ACCTGTTAAGGTTGC | 84749 |
rs114843421 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | USP30 | GRCh38.p7 | 12:109081718 | GAAGTCCACAAGTTC[A/G]TGCAGTTACATCCTC | 84749 |
rs114955626 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109050938 | CTTGAACCTGAGAGG[C/T]GAGATCGTGCCATTG | 84749 |
rs115078790 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | USP30 | GRCh38.p7 | 12:109034577 | TATTAAAAAAGAAAG[A/G]AAGAGAGAAAATGCA | 84749 |
rs115256972 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | USP30 | GRCh38.p7 | 12:109026921 | ACATAAGCATAAAGA[C/G]AAAGCAAGCTCTCTG | 84749 |
rs115287827 | snp | C/T | 0.081446 | 0.184634 | intron-variant | USP30 | GRCh38.p7 | 12:109036224 | AACTTTACGGATGCT[C/T]TTTATTTCCCCATGT | 84749 |
rs115332242 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055191 | TAGCAAAAGCATAAC[C/T]AGCGTTCAAGTCAAG | 84749 |
rs115336516 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | USP30 | GRCh38.p7 | 12:109045351 | GCCCATTCTCAGGTG[C/T]TAATGAGATCCCAGC | 84749 |
rs115461362 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | USP30 | GRCh38.p7 | 12:109026454 | TCATAGTCTTGGTGG[A/C]TTACACAACAGAATT | 84749 |
rs115531767 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | USP30 | GRCh38.p7 | 12:109080593 | CATATGTTCTTCTAC[A/G]TTTTGTTTAACATAG | 84749 |
rs115537452 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP30 | GRCh38.p7 | 12:109037436 | AACACAATTTTTACT[A/G]TTTTTCCCCCTGTGC | 84749 |
rs115798645 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | USP30 | GRCh38.p7 | 12:109043613 | TGCAAGACCTAAAAT[G/T]ATAAAACTCTTGGAA | 84749 |
rs115888966 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | USP30 | GRCh38.p7 | 12:109027307 | TTTTAGAGACAGGGT[A/C]TCACTCTGCTGTCCA | 84749 |
rs115991738 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | USP30 | GRCh38.p7 | 12:109025262 | AAATTCTCAGCCTCC[C/T]TAATTATGTTGGCCA | 84749 |
rs116068593 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | USP30 | GRCh38.p7 | 12:109032600 | CAACATCCAGAATAG[A/G]CAAATCCATAGAGAC | 84749 |
rs116123141 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | USP30 | GRCh38.p7 | 12:109079255 | TCTTCAATCTTTCTT[C/G]TGTGTGTTCTTTAAA | 84749 |
rs116161169 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | USP30 | GRCh38.p7 | 12:109024253 | TGCAATGGTTAAATT[A/C]ATTTATTTTAATTTT | 84749 |
rs116162393 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP30 | GRCh38.p7 | 12:109033751 | GGGAGCAGGTAAGTA[C/T]CTCTTGACTTTGCCA | 84749 |
rs116299765 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | USP30 | GRCh38.p7 | 12:109065170 | AGGCTGGCCTACTGT[A/G]TCTTGGGAGTCACTG | 84749 |
rs116377959 | snp | C/T | 0.00795532 | 0.062565 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109021985 | CCCACCTCAACCTCC[C/T]TAGTAGCTGGGATCA | 84749 |
rs116524823 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053727 | CAGATCTTTTCATCC[C/G]CAGGCCCCACCACTC | 84749 |
rs116609778 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | USP30 | GRCh38.p7 | 12:109060029 | GATCTCATCAGACCT[C/T]GGAAGCTAAGCCGGG | 84749 |
rs116693997 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109066693 | CTGTTTCAAAAAAAA[A/G]GAAAAGTACACTACT | 84749 |
rs116839544 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109047247 | CGATGTTTACCCTAC[A/T]CTTCATCCTCTTCTG | 84749 |
rs116871037 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109031616 | GTGTCCATCAATAGA[C/T]GAATGGATAAACAAA | 84749 |
rs117073896 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053094 | GTGCCTCCTAGGCCT[G/T]CCAAGACCCCTCAAT | 84749 |
rs117402507 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | USP30 | GRCh38.p7 | 12:109024609 | AAGGAATACCTAGAG[A/T]ACTGGTAAAGCAGCA | 84749 |
rs117410636 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | USP30 | GRCh38.p7 | 12:109084763 | TTTCCTATTTGGGAT[C/T]AAGACAGATTATCCC | 84749 |
rs117536257 | snp | A/G | 0.155656 | 0.231515 | intron-variant | USP30 | GRCh38.p7 | 12:109028338 | GACTCACAGTCTGCA[A/G]GCTGTACAGGAAGCA | 84749 |
rs117645666 | snp | A/G | 0.0441095 | 0.141807 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109087529 | GTCCTGCACTCACCC[A/G]ATGCAGACCTTGACT | 84749 |
rs117658137 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | USP30 | GRCh38.p7 | 12:109035861 | AGATACACAAAAAAA[G/T]TATATACAAAAAATA | 84749 |
rs117705396 | snp | A/G | 0.0170979 | 0.0908987 | intron-variant | USP30 | GRCh38.p7 | 12:109067649 | ACAACATTTGAACAG[A/G]TTTAGCTTGGAGAAT | 84749 |
rs117925202 | snp | C/G | 0.0505692 | 0.150756 | splice-donor-variant | USP30 | GRCh38.p7 | 12:109047715 | CTCAGAGTGTGTTGG[C/G]TAAGTGTGGCATTTA | 84749 |
rs117993355 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | USP30 | GRCh38.p7 | 12:109045330 | CCATTTCCTATCCTC[C/T]CTTTAGCCCATTCTC | 84749 |
rs118053440 | snp | C/G | 0.200182 | 0.244986 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109051519 | CCCCCCACCCCCACC[C/G]CCCGGCCTCCCAAAG | 84749 |
rs137964396 | snp | A/G | 1.6666e-05 | 0.00288664 | missense, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088240 | ATTTTACGAAAAGTC[A/G]GATTCACCCGTGGAG | 84749 |
rs137991609 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | USP30 | GRCh38.p7 | 12:109037503 | TTATTTTTTATTGAA[A/T]GCTGAGCATTTTATA | 84749 |
rs138008736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109060456 | CAGAAATCTTTATGA[A/G]GCAAGTGTACTTTTC | 84749 |
rs138009323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109070444 | GTCTGAGCACAGCCC[A/G]AAATGGGAATAAGCT | 84749 |
rs138046993 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP30 | GRCh38.p7 | 12:109056874 | CAAAGAAGGTGGGGA[A/G]GTTGGTCATATTTGT | 84749 |
rs138115233 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109047527 | TCTGTGTTTATTCTT[C/T]CTACCTGTGGACAAA | 84749 |
rs138122046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109063393 | GGCGTGAGCCACCAC[A/G]CCAGGCCTAGGCTGA | 84749 |
rs138171698 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109080920 | TAGGTTCTTGTAAGC[A/G]CGCTCTGCGATGTTT | 84749 |
rs138179623 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | USP30 | GRCh38.p7 | 12:109026067 | CATGATTCTTTTAAA[C/T]AATTTTTTAATTAAA | 84749 |
rs138193365 | in-del | -/TTG | 0.472981 | 0.113046 | intron-variant | USP30 | GRCh38.p7 | 12:109056176 | GATTTGACTTAGTTT[-/TTG]TTGTTGTTGTTGTTG | 84749 |
rs138327076 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109056045 | GAACAGCAGTGCAAA[C/T]GCCTTGAGGTCAGAG | 84749 |
rs138385201 | snp | A/G | 0.000791413 | 0.0198766 | missense | USP30 | GRCh38.p7 | 12:109071676 | GAGACCGCCAGCCTC[A/G]GGTCACACATTTGTT | 84749 |
rs138385845 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109074899 | CCCCAGCCCCTGGCA[A/G]CCAGCATGTACTCTG | 84749 |
rs138418425 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP30 | GRCh38.p7 | 12:109071154 | CAGTGTTTAACAGAT[A/G]TGGAGTTTCAGCTGG | 84749 |
rs138446018 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053190 | CCCCAACCTTGGCAC[C/G]GTTCTTCTAGTCCTA | 84749 |
rs138562273 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109032371 | TTATTCATAACAGCC[A/G]AAAATTGGAAACAAG | 84749 |
rs138596489 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109036632 | AAGTCTCTGTTTTTT[-/T]GTTTTGTTTAAGAAT | 84749 |
rs138697639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109074974 | CAGGTGGTGTTTATC[C/T]TTCTATATCTGGCTT | 84749 |
rs138722814 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109032603 | CATCCAGAATAGGCA[A/T]ATCCATAGAGACAGA | 84749 |
rs138755643 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109085288 | ATTTACATATGCATA[G/T]GTATGTGTGTATATA | 84749 |
rs138775923 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109066358 | AATAAGCCCATCAAA[C/G]TTTTATTAGGCCTGA | 84749 |
rs138781756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109044687 | ACAAATTTTATGTTA[C/T]ATGTACTTTGCCACA | 84749 |
rs138788110 | snp | C/G | 0.200182 | 0.244986 | intron-variant, upstream-variant-2KB, downstream-variant-500B | USP30, USP30-AS1 | GRCh38.p7 | 12:109051716 | CTGGAATTACAGGAG[C/G]CTGCCACCACGCCCG | 84749 |
rs138932775 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109029860 | TAGAAGGTAGGGTGA[A/G]AGGGGCAACCTTTGA | 84749 |
rs138938617 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109079245 | TGTTCAATTTTCTTC[A/G]ATCTTTCTTCTGTGT | 84749 |
rs138942249 | in-del | -/T | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109051250 | AATTTTACCTCTTGC[-/T]TTTTTTTTTTTTTTT | 84749 |
rs138947322 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046737 | AGTCTCACTTTGTCG[C/T]CCAGGCTGGAGTGCA | 84749 |
rs139005476 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109021511 | CAAAGATCACTCATT[C/G]TTTCAACAAGCGTTA | 84749 |
rs139010817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109083772 | TGTCTGCTGCCCCCA[A/G]TTAGGTCAGGATTGT | 84749 |
rs139031766 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109081152 | TAGTATTATTGTACC[A/T]CTTATGTGTACAAGG | 84749 |
rs139043869 | snp | A/G | 0.00154875 | 0.0277845 | intron-variant | USP30 | GRCh38.p7 | 12:109085652 | AAACCCCTGACATGT[A/G]TTCGTATCATTCAGC | 84749 |
rs139135839 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109047293 | CACAAACTTGTCTGG[A/G]GAGAAGGGTGAATCA | 84749 |
rs139195292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109030914 | CCACCGTGCCAGGCC[A/G]ATTGTGATTCTTTTA | 84749 |
rs139278674 | snp | A/C | 4.95029e-05 | 0.00497484 | synonymous-codon | USP30 | GRCh38.p7 | 12:109082896 | CTGGTCCAGCCACGG[A/C]ACGCCTCTGAAGCGG | 84749 |
rs139314514 | snp | C/G | 3.29473e-05 | 0.00405864 | missense, utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109067580 | GCAAGCTGCTTGTTG[C/G]ATGTCTTAAGAATGT | 84749 |
rs139322262 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | USP30 | GRCh38.p7 | 12:109039277 | AATTTGCATGTCTTG[C/T]TACATTCTTTTACAA | 84749 |
rs139339671 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109072603 | CTTTCTTTTTACCTT[G/T]TTGAATTGATCCTGG | 84749 |
rs139412637 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109051442 | TTGTATTTTTTAGTA[A/G]AGACGGGGTTTCACC | 84749 |
rs139421450 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053599 | AGCAGGTTTAAAGAG[C/G]TTATTATCCCAGGGC | 84749 |
rs139446347 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109048822 | GCAGGGGTGTGTAAC[G/T]CAATCCTTGCTTGGC | 84749 |
rs139553188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109027169 | TTATATAACCATCAC[A/G]CTATTGACTTCCAGA | 84749 |
rs139616372 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109057587 | ATTAAAGAAGAAAGA[C/G]AGCATGTAGGGGAGA | 84749 |
rs139702104 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109036322 | CTTTTTTTTTTTTTT[A/T]GGGAGTCTCACCCTT | 84749 |
rs139763462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109034588 | AAAGAAAGAGAGAAA[A/G]TGCATTCTGCTGCTG | 84749 |
rs139772885 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109075758 | TGAGTGCCTTTTCAT[A/G]TACCCACTGGCCATT | 84749 |
rs139832160 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109024217 | CACACACTTGGATGG[C/T]ACATAATAAGTGTTA | 84749 |
rs139881344 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP30 | GRCh38.p7 | 12:109064208 | AGTTTTAGAAGTTCT[A/G]AGTTCATATATTCTG | 84749 |
rs139902731 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109063722 | TTTCTGTTTTTATTG[A/T]TAGTAGCCATCCTAA | 84749 |
rs139904680 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | USP30 | GRCh38.p7 | 12:109031578 | GCATTATTCACAATA[C/G]CCAAACAGTGGAAGC | 84749 |
rs139925498 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109061310 | GGGACCCAGTGCTGG[A/G]AGCCAGAGCCATCCT | 84749 |
rs139956606 | snp | C/T | 0.000230601 | 0.0107353 | synonymous-codon | USP30 | GRCh38.p7 | 12:109081965 | GGACCACTGCCTTCA[C/T]CACTTCATCTCATCA | 84749 |
rs139989233 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109034053 | AGAGGTAATTCAGAA[A/G]CTGGTAAACCTGTCC | 84749 |
rs140039464 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109067813 | AGATACAGCTGTTTT[C/T]CACTCAGTGGATGGA | 84749 |
rs140114893 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109045823 | ATAGAACGCGTGTGT[A/T]TGTGTGTGTATGCAC | 84749 |
rs140134127 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109076538 | ATTTGGTGTTTTATA[A/G]TTAAGTATGATATTA | 84749 |
rs140198663 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109047932 | AGGGTGCTCAAGACC[C/T]TTTTAGGAGGTTCAC | 84749 |
rs140215254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109043466 | ACAAGAGTACCAATA[C/T]GATTGAATGGGAAAA | 84749 |
rs140240855 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | USP30 | GRCh38.p7 | 12:109065033 | ATTTTTTTAAGTGAA[A/C]GCAAGTTTATTAAGA | 84749 |
rs140263989 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109025408 | GAGCTCTGACTAATA[C/G/T]AGTGCTTATCATTAT | 84749 |
rs140343259 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054446 | GGATCACCTGAGCCC[A/G]GAAGGTGAAGATTGT | 84749 |
rs140371213 | in-del | -/CGGCGG | 0.498734 | 0.0251279 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052621 | TCGTATCCCTCGGTC[-/CGGCGG]CGGCGGCGGCGGCGG | 84749 |
rs140414657 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109070052 | TAGGAGGCTGCGGGC[A/G]GCATCAGCTTCTATT | 84749 |
rs140534771 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB, downstream-variant-500B | USP30, USP30-AS1 | GRCh38.p7 | 12:109051785 | ATGTTGGCCAAGCTG[A/G]TCTCGAACTCTTGAC | 84749 |
rs140552861 | snp | A/C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109037163 | GGAACTATCTTCATG[A/C/T]TCATTGATACTTTGC | 84749 |
rs140598342 | snp | C/T | 0.00517822 | 0.0506191 | utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109024971 | AAGAGGAGATTGCTG[C/T]GTGAGTCTGAGTGGA | 84749 |
rs140636378 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109025876 | TATTTTTTGTAGAGA[C/T]GGAGTTTTGCTTCAT | 84749 |
rs140637519 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109058889 | TTGCAGCCCTGTCCA[G/T]CTGTTGGACAATACA | 84749 |
rs140726743 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | USP30 | GRCh38.p7 | 12:109039841 | ATCTCGATCTCTTGA[A/C]CTCATGATCTGCCTG | 84749 |
rs140769082 | snp | A/G | 8.2573e-05 | 0.00642493 | missense, synonymous-codon, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088454 | CAATGGGGCTCCCAG[A/G]GGCCAGTTCTCTTTC | 84749 |
rs140782274 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109069607 | ATGGAGTCGTAGCAG[C/T]AGACATGACTTGCAG | 84749 |
rs140820667 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109066069 | CCAGCCTGGGCAACA[C/T]GGTGAAACTCTGTCA | 84749 |
rs140831073 | snp | C/G/T | 0.000344944 | 0.0131291 | intron-variant, synonymous-codon | USP30 | GRCh38.p7 | 12:109083082 | GTGCGCGCGAGGAGC[C/G/T]GATGCAGCAGGAATT | 84749 |
rs140936395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109059112 | AACAAGTTTAGGAAT[A/G]GCTGAATGGTAGCCC | 84749 |
rs140951559 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | USP30 | GRCh38.p7 | 12:109040659 | TCAAGATGGTGCACT[C/G]ACGTGATTGGCAAGT | 84749 |
rs141056343 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109063047 | GTCTTCAGGGTTCAT[C/T]CATGTTATACCATGT | 84749 |
rs141059579 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant | USP30 | GRCh38.p7 | 12:109058032 | GCTGGAAGAGTTCAC[C/T]TCCCAGTACTCCAGG | 84749 |
rs141158940 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109060691 | GATGAGTCTCGTCTT[A/G]TCACTCAGGCTGGAA | 84749 |
rs141202526 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP30 | GRCh38.p7 | 12:109083613 | ATGATTGGTCCAAGG[A/G]CAAACACCACACAGG | 84749 |
rs141238648 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109081047 | TGTTGATGAATATTC[C/T]TGTAGTTATGCCCAT | 84749 |
rs141319730 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046888 | TTTTAGTAGAGACGG[G/T]GTTTCACCATGTTGG | 84749 |
rs141319795 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109079990 | AATTAATTTTCTTCT[G/T]GCCTGCAGTTAACCT | 84749 |
rs141354738 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP30 | GRCh38.p7 | 12:109042556 | TTCATAGCTACATAG[C/T]ACTCTCCTGTGTGGG | 84749 |
rs141359955 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | USP30 | GRCh38.p7 | 12:109078180 | TCTGTAATCCCAGCA[C/G]TTTGGAAGGCTGAGA | 84749 |
rs141401789 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | USP30 | GRCh38.p7 | 12:109078314 | CTGTAATCCCAGCTA[C/T]TCGGGAGGCTGAGGC | 84749 |
rs141490059 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP30 | GRCh38.p7 | 12:109049254 | TCTAGCTTTTGATTT[A/G]AAGTGAGAGATGTGC | 84749 |
rs141513064 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109026614 | AGTAGACCGTAGGTG[C/T]GCACCACCATGCCCA | 84749 |
rs141551427 | snp | C/G | 0.00746264 | 0.060627 | intron-variant | USP30 | GRCh38.p7 | 12:109072265 | GTGAAAGGGATTATA[C/G]TAAGGTTTTCAGTCT | 84749 |
rs141710397 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055584 | TTTGTATTTTTAGTA[A/G]AGACAGGGTTTCACC | 84749 |
rs141721199 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109034538 | TCAAGACCAGCCTGG[A/G]CAACATAGTGAGACC | 84749 |
rs141817954 | snp | A/G | 0.000924809 | 0.0214837 | missense | USP30 | GRCh38.p7 | 12:109085024 | CCATCTTTATTGCCA[A/G]CGCTGTCAGCGCCGA | 84749 |
rs141848154 | snp | A/G | 3.29902e-05 | 0.00406128 | missense, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088297 | CTGTGGTACCAGTGC[A/G]TGTTGGTCGGGTGGT | 84749 |
rs141883832 | snp | A/G | 1.6516e-05 | 0.00287362 | missense | USP30 | GRCh38.p7 | 12:109071621 | TGACAGGATGCTCAC[A/G]AATTATTCCATGTCA | 84749 |
rs141896486 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP30 | GRCh38.p7 | 12:109038430 | TTTGGGTTGAATCCA[C/T]GTCATTGCTATTGTA | 84749 |
rs141935506 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB, nc-transcript-variant | USP30, USP30-AS1 | GRCh38.p7 | 12:109052419 | AACCAAGCAGCCCCA[C/G]GCAACTGAGCCCAGC | 84749 |
rs141942386 | snp | A/G | 0.0193772 | 0.0965046 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022888 | GTGTCTGTCACAATG[A/G]TAGTTTGAACTTATT | 84749 |
rs142119844 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP30 | GRCh38.p7 | 12:109048055 | TGATGTGATCATGGG[C/T]CTGACGTCTAATAGA | 84749 |
rs142149416 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109074246 | TATTGCATTACATGG[A/G]TCTACAACATTTTTA | 84749 |
rs142164192 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054315 | TTCTTGAGCTCAGGA[C/G]TTCGAGACCAGCCTG | 84749 |
rs142196889 | snp | A/C | 0.00199481 | 0.0315187 | utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109025057 | GAGGCCCAGACAGAA[A/C]AGAAACAGAGGAAAG | 84749 |
rs142206796 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | USP30 | GRCh38.p7 | 12:109050133 | ACCCTGTCTCTACTA[A/C]AAATACAAAAATTAA | 84749 |
rs142270967 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP30 | GRCh38.p7 | 12:109032041 | TAGGCAGTCAAAGCT[A/G]CAGTGAGCCATGATT | 84749 |
rs142311198 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP30 | GRCh38.p7 | 12:109077457 | ATCTCTGCTAAGACT[C/T]CTTGACTTGAAGTCT | 84749 |
rs142419114 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109064822 | CCCCATAGTATTTTA[C/G]ACAAAGTTGGGTTAA | 84749 |
rs142477859 | snp | C/G/T | 0.00105954 | 0.0229926 | missense, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088262 | CCCGTGGAGCCAGAA[C/G/T]CTTCTTTCTCACGGG | 84749 |
rs142506422 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109079300 | TTGACTTATCTTCAC[A/G]TTCACTGATTCTTTT | 84749 |
rs142522281 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109032484 | AAATGCAGTACTGAT[A/T]ATGGTGTAATATGGA | 84749 |
rs142562945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109060921 | AAAGTGTTGGGATTA[C/T]AGGCGTGAGCTACCA | 84749 |
rs142597191 | snp | C/G | 1.64928e-05 | 0.00287161 | synonymous-codon | USP30 | GRCh38.p7 | 12:109073457 | ACCTCACCCTACATC[C/G]AATCACTGGAAGTCT | 84749 |
rs142610740 | snp | A/C/T | 6.73757e-05 | 0.00580379 | intron-variant | USP30 | GRCh38.p7 | 12:109082813 | GCCCCTGAAACAACT[A/C/T]GGTTCTCCCGATTTC | 84749 |
rs142616630 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | USP30 | GRCh38.p7 | 12:109028129 | TAACAATGTTGAGCA[C/T]CTTTTCATGTGCTTA | 84749 |
rs142625500 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109063597 | TCAAATGGTAATTCT[A/G]TTTAATTTTTTGAGG | 84749 |
rs142669866 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | USP30 | GRCh38.p7 | 12:109036090 | GCTTGAGACCAAGAG[C/G]TTGAGGCTGAAGTGA | 84749 |
rs142694522 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | USP30 | GRCh38.p7 | 12:109085316 | ATATGTGTGTATGTA[A/T]AAAATATAAAGAAAA | 84749 |
rs142729108 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109053354 | GTTTTGCAAGGGTCT[A/C]TAAATTGGTCAGGGC | 84749 |
rs142768442 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | USP30 | GRCh38.p7 | 12:109026220 | AGCTGGGACTGCAGG[C/T]GCATGCCATCACACC | 84749 |
rs142788785 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP30 | GRCh38.p7 | 12:109058982 | CACAATAATAGCTTG[C/T]GAAATACTCAGTACT | 84749 |
rs142951729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109075916 | TATTTCAAGTATTCA[A/G]TTTTGGATATTAACC | 84749 |
rs142952589 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109045746 | GTTGCAATCAGTATG[C/T]TTCAGGTGAGGAAAC | 84749 |
rs143081358 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | USP30 | GRCh38.p7 | 12:109060632 | ACTGATTTTAAATGC[A/G]AAAATAGAAAAACTG | 84749 |
rs143097197 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109044932 | ATGGGGGAAAAAATG[-/T]TTTCTGATTATAGTT | 84749 |
rs143104227 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | USP30 | GRCh38.p7 | 12:109024100 | GAGCAGGTTGTCTAA[C/T]TTTCCGTGCTTGCAT | 84749 |
rs143154709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109073220 | GGCTCTACCCATTAT[A/G]CAGAAACCGTATATA | 84749 |
rs143172617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046712 | GCTGCTGTTGTTGTT[A/G]TTGAAATGGAGTCTC | 84749 |
rs143218616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109042616 | TGCTTCCAATCCCTT[A/G]TTATTAAAAACAATG | 84749 |
rs143232892 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109056509 | ACTTAGATTTTAAAT[A/C]CTAATGTCTAAACAT | 84749 |
rs143276254 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022711 | AGGCTTTCTCTGAGT[A/G]TCTCAAAAGAAACCA | 84749 |
rs143379058 | snp | A/C/G | 0.00318978 | 0.0398085 | intron-variant | USP30 | GRCh38.p7 | 12:109026221 | GCTGGGACTGCAGGC[A/C/G]CATGCCATCACACCT | 84749 |
rs143391590 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109031894 | GGATTGCTTGAGCTC[A/G]GGAGTTCGAGACCAG | 84749 |
rs143397780 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109056151 | TGAGAAGTAGCCTTT[A/G]GAATGTGATGATTTG | 84749 |
rs143414748 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109087478 | CTCCAGGCTCTGGGC[A/G]TCAGGGTGCAAGGGG | 84749 |
rs143487979 | snp | A/C | 1.64749e-05 | 0.00287005 | synonymous-codon | USP30 | GRCh38.p7 | 12:109082016 | GTGTGACAACTGTAC[A/C]AAGGTATGCATTGAA | 84749 |
rs143566199 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109060568 | CAACTCGCTGCCAGC[A/G]TTCATCTAATTTTAC | 84749 |
rs143588438 | snp | C/T | 8.51216e-05 | 0.00652331 | intron-variant | USP30 | GRCh38.p7 | 12:109073562 | AACACTTGATATTTC[C/T]GGGAGAGGTTTTCCA | 84749 |
rs143646698 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | USP30 | GRCh38.p7 | 12:109070640 | GGCAGTGTGAGGGGA[A/C]ACCAAAGGAGAAGCA | 84749 |
rs143667153 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | USP30, USP30-AS1 | GRCh38.p7 | 12:109054515 | ACTAGAGCAACTAGA[A/G]CAAGACACTGTCTCA | 84749 |
rs143694877 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109049637 | CTGGCCAACACAGTG[A/G]AACCCCATCTCTACT | 84749 |
rs143713502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109080756 | AATACTTTATTGGTA[C/T]GGTACCTTTTCTGTT | 84749 |
rs143757548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109029905 | ACCCTATCTGTTAAG[A/G]CCTCTGAGAAAGTTC | 84749 |
rs143812976 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046296 | TTATTTTGTATTTTA[C/G]TAGAGACAGCGTTTC | 84749 |
rs143820774 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | USP30 | GRCh38.p7 | 12:109084493 | TTTTTGGTTATCACT[A/G]CTGGGGGAGGGGTGC | 84749 |
rs143830379 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP30 | GRCh38.p7 | 12:109071377 | TCATAGACTGCTGGC[A/G]TGAAGGCAGCCACCT | 84749 |
rs143893760 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP30 | GRCh38.p7 | 12:109041561 | AATCGCTTGAACCTG[A/G]TAGGTGGAGGTTGCA | 84749 |
rs143900827 | in-del | -/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109028461 | GGAGGTGCCACACCC[-/T]TTTTTTTTTTCTGTT | 84749 |
rs143919521 | in-del | -/CC | | | intron-variant | USP30 | GRCh38.p7 | 12:109073940 | TTTATTTTATTTTTT[-/CC]CACAGCCATTACTGA | 84749 |
rs143994170 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP30 | GRCh38.p7 | 12:109030082 | TCTTCCTGCAAGTTA[C/T]GCTGTAAGATTAAGG | 84749 |
rs144028464 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP30 | GRCh38.p7 | 12:109068291 | TTCCAAGATGGCCTT[A/G]TCCAGCTTCGTGTAG | 84749 |
rs144115468 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109058398 | ACATGGAGAAACTCC[A/T]TCTCTACTAAAAACA | 84749 |
rs144165163 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109086024 | GTGCAAGCGGCCCCA[A/C]TAGAGCCTTCCAGCC | 84749 |
rs144240550 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109082215 | GTTTTGTTTCATGCA[C/T]AGTGTTTAAAGAATA | 84749 |
rs144243812 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109028663 | TTGTAATTTTAGTAG[A/T]GAGGGGTTTCACCAT | 84749 |
rs144434526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109072809 | CATGCTGTTTGCCAG[A/G]CATTGCATTATCTCA | 84749 |
rs144484410 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109079269 | TCTGTGTGTTCTTTA[A/G]ATTAGATCATTTCTA | 84749 |
rs144488199 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109079590 | AGGTTGGTCCTGAAC[A/T]CCTGGGCTCAAGTGA | 84749 |
rs144500722 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | USP30 | GRCh38.p7 | 12:109032876 | GGTTTTATTTCACAC[C/T]AGAGCAATGCATCAT | 84749 |
rs144594902 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | USP30 | GRCh38.p7 | 12:109027796 | ATCCATTCATCTGTT[G/T]ATGGACACGTGGGTT | 84749 |
rs144599763 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP30 | GRCh38.p7 | 12:109040661 | AAGATGGTGCACTCA[C/T]GTGATTGGCAAGTTG | 84749 |
rs144619219 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109037765 | CCAGTCTTTGCCAAG[A/G]AGTGCCGTGTGTGTT | 84749 |
rs144633654 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109057740 | GTGCTTACAGTCTGC[A/G]GAGCAGTACTAGAAC | 84749 |
rs144634695 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | USP30 | GRCh38.p7 | 12:109041626 | GGTGACAGAGCGAAA[C/T]TCCATTTCAAAAAAA | 84749 |
rs144639687 | snp | C/G | 9.89283e-05 | 0.00703238 | missense, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088307 | AGTGCGTGTTGGTCG[C/G]GTGGTTCATCATTAG | 84749 |
rs144830211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109075743 | GATGATTAGTGATAT[C/T]GAGTGCCTTTTCATA | 84749 |
rs144845334 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP30 | GRCh38.p7 | 12:109066071 | AGCCTGGGCAACATG[A/G]TGAAACTCTGTCACT | 84749 |
rs144872117 | snp | A/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046639 | CACACCCAGGGAAAA[A/T]GATGAATTGCCTAGG | 84749 |
rs144879645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109039907 | AACCACCACACCTGG[C/T]CAGCCATTTTCTTTC | 84749 |
rs145015698 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109049935 | TTGCTGTAGTCAGGT[A/T]GCCACAAACCTTGAA | 84749 |
rs145026925 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP30 | GRCh38.p7 | 12:109083660 | TGCCATGTTGGGCCA[C/T]TTTCTAAAGGTGTCT | 84749 |
rs145060605 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB, downstream-variant-500B | USP30, USP30-AS1 | GRCh38.p7 | 12:109051645 | CATGATCTTGGCTCA[A/G]TGCAACCTCCACCAC | 84749 |
rs145089945 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | USP30 | GRCh38.p7 | 12:109077450 | CCTCTTCATCTCTGC[G/T]AAGACTCCTTGACTT | 84749 |
rs145143813 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109081130 | TCAGTTGTTCCAAGC[A/G]ATTCTTTAGTATTAT | 84749 |
rs145235503 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB, downstream-variant-500B | USP30, USP30-AS1 | GRCh38.p7 | 12:109051615 | GGTTCTGTCACCCAG[A/G]CTGGAATGCAGTGGC | 84749 |
rs145261386 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109062127 | TTTAGTAGAGATGGG[A/G]TTTCACACTGTTGCC | 84749 |
rs145270687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109050944 | CCTGAGAGGCGAGAT[C/T]GTGCCATTGCACTGC | 84749 |
rs145279323 | snp | A/G | 1.64909e-05 | 0.00287144 | missense | USP30 | GRCh38.p7 | 12:109082930 | GAGCACGTGCAGTTC[A/G]ATGAGTTCCTGATGA | 84749 |
rs145359179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109065775 | CAACACAAAGGTCAG[A/G]AAGCAGTGGCCATGC | 84749 |
rs145374160 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109042049 | AATTTTACCACAGAG[A/C]GATAACCCAGAGTGA | 84749 |
rs145382338 | snp | A/C | 0.0100332 | 0.0701137 | synonymous-codon, utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109067525 | TTTTTTGTTTCCAGC[A/C]TTGTCCTGCCAAGAA | 84749 |
rs145439261 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | USP30 | GRCh38.p7 | 12:109073228 | CCATTATACAGAAAC[C/T]GTATATAAAGATAGA | 84749 |
rs145585568 | snp | A/C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022282 | GATCCATGATGGCAA[A/C/G]TGGCAAAAGCTATGA | 84749 |
rs145633102 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109064481 | AGTTGATGGTTCACC[A/G]TGTTGGCCAGGCTGG | 84749 |
rs145633628 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | USP30 | GRCh38.p7 | 12:109025969 | GCATTACAGGTGTGA[G/T]CCACTGACCCTGGCA | 84749 |
rs145654798 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | USP30 | GRCh38.p7 | 12:109055969 | AGGCCTCTTGAGAAG[C/T]GAAGGGAGGTAAAGG | 84749 |
rs145654817 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109023052 | GCTAAGAGGGTGGAC[A/G]CTTATCTAAAGACAT | 84749 |
rs145720570 | snp | A/G/T | 0.00113713 | 0.0238188 | missense | USP30 | GRCh38.p7 | 12:109071667 | AAGATGAGCGAGACC[A/G/T]CCAGCCTCGGGTCAC | 84749 |
rs145751539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109025609 | CATATGAGTATCTCA[C/T]ATAGAAATTTGCCTG | 84749 |
rs145761955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109034964 | TTGGTTGCTGTTTGA[A/G]TGATACCACTTTTTC | 84749 |
rs145858100 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | USP30 | GRCh38.p7 | 12:109085261 | AAATTAAAAATTTTT[A/T]AAGTACATAAAATTT | 84749 |
rs145872618 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109060044 | CGGAAGCTAAGCCGG[A/G]TAGTGGTTGGCTAGC | 84749 |
rs145877731 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | USP30 | GRCh38.p7 | 12:109039911 | ACCACACCTGGCCAG[C/G]CATTTTCTTTCTTTC | 84749 |
rs145943045 | snp | A/C | | | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022148 | AGATGTGAGCCATTG[A/C]GCCCGGCCTCAGGGT | 84749 |
rs145985149 | snp | A/C/G | 0.000874025 | 0.0208868 | missense, synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088293 | AAGACTGTGGTACCA[A/C/G]TGCGTGTTGGTCGGG | 84749 |
rs146012366 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | USP30 | GRCh38.p7 | 12:109061309 | TGGGACCCAGTGCTG[G/T]GAGCCAGAGCCATCC | 84749 |
rs146019668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109033849 | CAACTTTAAGGAGTC[C/T]CTGGGTCACATAGCT | 84749 |
rs146031591 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP30 | GRCh38.p7 | 12:109031374 | AGTTTTTTTCCAGAG[C/T]ACATCATCTTCACTT | 84749 |
rs146031889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109063644 | TCCACAGATGGTGCA[C/T]GATTTTATAATTCCA | 84749 |
rs146052645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109074407 | GAGTAGAATTGCTAG[C/T]TTATATGGTAACTCT | 84749 |
rs146142615 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109047610 | ACACTAAGACCCAGC[A/G]CTGAGGACAAAAGGA | 84749 |
rs146154108 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109078867 | GGTTGACAGTGTTGC[C/T]GTGGTTTTGCTTTGG | 84749 |
rs146189359 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109077618 | CAATCTTTTAGTTGG[A/C]ATGCTTAGTCCATTT | 84749 |
rs146394744 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | USP30 | GRCh38.p7 | 12:109050226 | TTGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 84749 |
rs146457884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109068908 | TCAGCGATCCAGTCA[A/G]TCAGGAGCAGATTTT | 84749 |
rs146498790 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP30 | GRCh38.p7 | 12:109028236 | ATTTTTGCTGTTGAG[C/T]TGCAGGAATATTCTA | 84749 |
rs146570482 | snp | A/G | | | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109087564 | TGTTGAAATGAACAC[A/G]CTTGTTTTACCCAAG | 84749 |
rs146572489 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109031975 | GGTGTCATGGTGTGC[A/T]TCTGTAGTCCCAGCT | 84749 |
rs146581765 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109083310 | ACAGAGAGAAACGCT[A/T]AAAATTGCAGCTTTG | 84749 |
rs146583618 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109028675 | TAGAGAGGGGTTTCA[C/T]CATGTTGACCAGGCT | 84749 |
rs146700962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109043213 | CTCTGTCAAAATCCC[A/G]TTTACTTTTTGAAGA | 84749 |
rs146749886 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109036238 | TCTTTATTTCCCCAT[A/G]TGGGTTTGAATTACT | 84749 |
rs146810437 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109058568 | CAAGAGCGAAACTCC[A/G]TCTCAAAAAAAAAAA | 84749 |
rs147085487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109062726 | TGTGGCAAAATATCC[A/G]TAACATAAAATTTAC | 84749 |
rs147095513 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109060451 | TGACACAGAAATCTT[C/T]ATGAAGCAAGTGTAC | 84749 |
rs147123922 | snp | C/T | 0.000265719 | 0.0115234 | synonymous-codon | USP30 | GRCh38.p7 | 12:109085065 | TCTCCCAGTTGTTCC[C/T]GACTACAGGTGAGCC | 84749 |
rs147157850 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109030161 | CCTGCCCAGCTGTCA[A/G]TCATTGTGTACTGGG | 84749 |
rs147168538 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109027348 | CAGTGATGCAATCAC[A/G]GCTCACTGCAACCTC | 84749 |
rs147172706 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109082086 | TAGCGCCTCTCACAC[C/T]AGTGACCCTGAGCTC | 84749 |
rs147256943 | snp | A/G/T | 0.000904681 | 0.0212493 | intron-variant | USP30 | GRCh38.p7 | 12:109071570 | TCTGATCTTGCTCTT[A/G/T]CCTCTTCCAACCTCT | 84749 |
rs147263113 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | USP30 | GRCh38.p7 | 12:109044892 | ATCATTATGTTATCA[C/G]ACTTTTTCATGCTTT | 84749 |
rs147265701 | snp | A/C | 0.0337553 | 0.125452 | intron-variant | USP30 | GRCh38.p7 | 12:109032961 | ATAGAGACTGACAAG[A/C]TGCCCCTTAGCCTGA | 84749 |
rs147273459 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP30 | GRCh38.p7 | 12:109041584 | AGGTTGCAGTGAGCC[A/G]AGATAGTGCCACTGC | 84749 |
rs147320109 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | USP30 | GRCh38.p7 | 12:109067766 | CTGGGACCAGAGTAC[C/G]AACTTTGTTCCTGCT | 84749 |
rs147362241 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109085574 | ACTTACCATTGTATT[C/T]ATCCCCTATTTAACA | 84749 |
rs147368791 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109056555 | GTAATCCTATGACTA[A/T]ATGTTACTTTAACTT | 84749 |
rs147484028 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP30 | GRCh38.p7 | 12:109067307 | TATTTTTAGTGGAGA[C/T]GGAGTTTCACCATGT | 84749 |
rs147573930 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109024957 | TGTAAGGGTGTTTCA[A/G]GAGGAGATTGCTGTG | 84749 |
rs147603508 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | USP30 | GRCh38.p7 | 12:109049480 | AATAGTAACATTAAG[C/G]ATCACTGATCACAGA | 84749 |
rs147646389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109051042 | TCACATAGAAATGAC[A/G]TATTTTGTTTTTCTT | 84749 |
rs147678746 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP30 | GRCh38.p7 | 12:109039760 | GGACTACAGGTGCCC[A/G]CCACCACACCCAGTG | 84749 |
rs147708667 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP30 | GRCh38.p7 | 12:109062993 | TTAAGCGGACTCATA[C/T]AATATTCACCCTTTT | 84749 |
rs147740274 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP30 | GRCh38.p7 | 12:109035985 | TCAACATAGTGAGAC[A/G]TCATCTCTGCAAAAA | 84749 |
rs147781691 | snp | A/G | 0.0267878 | 0.112589 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109050769 | ATCCCAACACTTTGG[A/G]AGCCCGAGGCGGATG | 84749 |
rs147812265 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109077725 | TTTCTTGTTCCTCTG[G/T]TCCCCCTTCACTGGC | 84749 |
rs147845035 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109048929 | TTCAACATTAAGGCT[A/G]GTCAGCTGTTGTGTC | 84749 |
rs147855167 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109079868 | CATCTGTGAGGTCCT[C/T]GTGTGCTGACTTCTT | 84749 |
rs147887285 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP30 | GRCh38.p7 | 12:109064163 | AGGCATGAGCCACCA[C/T]GCTCAGCATTGTTTG | 84749 |
rs147931793 | snp | C/T | 1.71067e-05 | 0.00292456 | missense | USP30 | GRCh38.p7 | 12:109083059 | CCGGGAGCCCCCACA[C/T]CAGGTGTGTGCGCGC | 84749 |
rs147950796 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | USP30 | GRCh38.p7 | 12:109062518 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 84749 |
rs148060080 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109043755 | AATTTAAAACTTTTG[C/T]GCATCAAAAGACACT | 84749 |
rs148133362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109084551 | GGATGCTGTTCAACA[C/T]CCTCTAATGCACAGG | 84749 |
rs148176974 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB, nc-transcript-variant | USP30, USP30-AS1 | GRCh38.p7 | 12:109052197 | CTCTACTGATATCGT[C/T]AGAGATGGGCCTCAT | 84749 |
rs148186625 | snp | G/T | 0 | 0 | intron-variant | USP30 | GRCh38.p7 | 12:109060651 | ATAGAAAAACTGTTC[G/T]TGGAGTTCTTTCCTT | 84749 |
rs148234435 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109061410 | AAAAAAAAAAAAAAA[A/T]TTTTTTTTTTTTTTT | 84749 |
rs148271525 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109069977 | CAGGGAGGCCAGGGC[A/G]GGGAGGGCGGTGGAG | 84749 |
rs148322479 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109066735 | TTAGGCTGCTGCATA[C/T]AGCTTGATGCTTTGC | 84749 |
rs148329488 | snp | A/T | 0.00636936 | 0.0560724 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022751 | GGTATAGTAGGAGAA[A/T]TTGGAACTATTGAAA | 84749 |
rs148377443 | in-del | -/TG | | | intron-variant | USP30 | GRCh38.p7 | 12:109074706 | GATTTGATGTATGAC[-/TG]TGTGTGTGTGTGTGC | 84749 |
rs148441556 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | USP30 | GRCh38.p7 | 12:109079281 | TTAAATTAGATCATT[C/T]CTATTGACTTATCTT | 84749 |
rs148442535 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | USP30 | GRCh38.p7 | 12:109038554 | CAATGAATGCTATTT[A/C]TTAAAATACTTACCT | 84749 |
rs148490027 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | USP30 | GRCh38.p7 | 12:109028043 | CAATTTCTGCACATT[C/G]TCCTCAACACTTGTT | 84749 |
rs148493313 | snp | C/T | 0.00064538 | 0.017952 | synonymous-codon | USP30 | GRCh38.p7 | 12:109082713 | GGAACACCAGAGGAC[C/T]ACTTTTGTTAAACAG | 84749 |
rs148504183 | snp | A/C/G | 9.88882e-05 | 0.00703103 | missense, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088357 | GGCAGCCTGACCACC[A/C/G]CCACCCTCCTGGAGG | 84749 |
rs148582798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109045659 | CTAGGAGGGGCTGTT[A/G]GGAGGATGAAACAGG | 84749 |
rs148645985 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109050726 | AAACAAAAAAATAAT[C/G]GGCCGGGCGCGGTGG | 84749 |
rs148655015 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109087062 | GTTGCTCTAGGTCCA[C/T]ATTCTGAATTTATTC | 84749 |
rs148697799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054287 | GCTCTTTGGAAGGCT[A/G]AGGCAGGTGGATTTC | 84749 |
rs148720468 | snp | C/T | 0.000368127 | 0.013562 | intron-variant | USP30 | GRCh38.p7 | 12:109071575 | TCTTGCTCTTGCCTC[C/T]TCCAACCTCTCTAAA | 84749 |
rs148824380 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109073347 | TTTTTCTTAAGAGGT[A/C]GTTTCTACCACATGC | 84749 |
rs148878668 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022314 | AATGACCGTTGAATG[C/G]ACACTTACAAGGAAC | 84749 |
rs148965251 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109080527 | CTCACCCTACTTCAT[C/T]GTCTCCTTTTTTGCA | 84749 |
rs148982278 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP30 | GRCh38.p7 | 12:109068262 | ACATACAGGTGCATC[C/T]TCCACAGCCACACTT | 84749 |
rs148996950 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP30 | GRCh38.p7 | 12:109084470 | ACATTGGGCAGTGTC[C/T]GGTAACATTTTTGGT | 84749 |
rs149018445 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP30 | GRCh38.p7 | 12:109029874 | AGAGGGGCAACCTTT[A/G]ATTAACATTAATGGT | 84749 |
rs149034013 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046655 | GATGAATTGCCTAGG[A/T]TCACATAGCCAGCCA | 84749 |
rs149039075 | in-del | -/GGGGGGGG | | | intron-variant | USP30 | GRCh38.p7 | 12:109040685 | AAGTTGGTAATGGCT[-/GGGGGGGG]GTTGGCAGAAGGCCT | 84749 |
rs149085800 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109049505 | CACAGATCACCTTAA[A/T]AGGTGTAATAATAAT | 84749 |
rs149169531 | snp | A/G | 3.2981e-05 | 0.00406071 | missense | USP30 | GRCh38.p7 | 12:109082931 | AGCACGTGCAGTTCA[A/G]TGAGTTCCTGATGAT | 84749 |
rs149172256 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109032018 | AAGGTAGGAGGATCA[C/G]TTGAGCCTAGGCAGT | 84749 |
rs149187477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109064652 | GGCATTTGCTTCCAG[C/T]TCCTTGTCAAGATAA | 84749 |
rs149229739 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109056054 | TGCAAACGCCTTGAG[G/T]TCAGAGCATTGGCTG | 84749 |
rs149268209 | snp | C/G | 1.64942e-05 | 0.00287173 | synonymous-codon | USP30 | GRCh38.p7 | 12:109071677 | AGACCGCCAGCCTCG[C/G]GTCACACATTTGTTT | 84749 |
rs149282813 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP30 | GRCh38.p7 | 12:109032662 | GGTTGTGGAGGGGGA[A/G]ATGGAGATTGACTGC | 84749 |
rs149407992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109079265 | TTCTTCTGTGTGTTC[C/T]TTAAATTAGATCATT | 84749 |
rs149409535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109024383 | CCACCTCAGCCTCCC[A/G]AATAGCTGGGATTAC | 84749 |
rs149453224 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | USP30 | GRCh38.p7 | 12:109037511 | TATTGAATGCTGAGC[A/G]TTTTATATAATATAA | 84749 |
rs149523663 | snp | C/G | 4.15334e-05 | 0.00455686 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109085953 | CCTCCTGCAAGGCTA[C/G]AGCTGATGGCACTGT | 84749 |
rs149568252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109047560 | CAAATACATTATACA[C/T]GTTCATGTGAAAGCA | 84749 |
rs149619535 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109050697 | CTCCAAACTGAGAGG[G/T]ACTTAGTACCAAAAA | 84749 |
rs149671278 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109027726 | ATCTATCAGAACCTC[A/G]TTCTTTTATATGACT | 84749 |
rs149676170 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109048861 | AGATCCTGTTTATAA[C/T]TTGGTATCTTATTGC | 84749 |
rs149733451 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | USP30 | GRCh38.p7 | 12:109057661 | GTACATTTAGGAAGA[A/C]CCAAGCTGTGCTGGA | 84749 |
rs149787066 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP30 | GRCh38.p7 | 12:109034800 | TTGTATTTTGGGCCT[A/G]TATTGTTAAGTGCAT | 84749 |
rs149822716 | in-del | -/TG | 0.253264 | 0.249979 | intron-variant | USP30 | GRCh38.p7 | 12:109048734 | AACAGAGTGAGACTC[-/TG]GTCTCAAAAAAAAAA | 84749 |
rs149823257 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109068025 | TAAAAAATCAATCTT[C/T]GGAGCTTTGCTTAAA | 84749 |
rs149885926 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | USP30 | GRCh38.p7 | 12:109077384 | ACTTTGTTATTGGAT[A/G]CAAGCATATGTATTA | 84749 |
rs149937706 | in-del | -/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109044988 | AGTAAGGTCAAACAT[-/C]TTTTTTTTTTTTTTT | 84749 |
rs149937801 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP30 | GRCh38.p7 | 12:109080100 | ACTTTTTGCCAGGCT[C/T]CCTGGAGTTTCCCCC | 84749 |
rs149946971 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109030997 | ATTTTTAAAATCAGG[A/G]GATGCTGAGCAAAGG | 84749 |
rs149996818 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109061820 | ATACTCAACCCTGCT[C/G]CCCTCCACCTTTCCC | 84749 |
rs150001845 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109083306 | AAGTACAGAGAGAAA[C/T]GCTTAAAATTGCAGC | 84749 |
rs150004182 | snp | C/T | 0.000181463 | 0.00952357 | missense | USP30 | GRCh38.p7 | 12:109082901 | CCAGCCACGGCACGC[C/T]TCTGAAGCGGCATGA | 84749 |
rs150034759 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109042005 | AAATAATATGAAACA[A/G]CATTCAGGAGAAAAT | 84749 |
rs150149532 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109051511 | AATCCGTGCCCCCCA[C/T]CCCCACCCCCCGGCC | 84749 |
rs150201990 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109029556 | GGCACACTGTTTTAC[C/T]AGGGCCCATTGTATG | 84749 |
rs150207491 | in-del | -/G | 0.0611083 | 0.163768 | intron-variant | USP30 | GRCh38.p7 | 12:109067977 | AGGCCCAGAGGTTTA[-/G]GTAAGATTTTTCTGG | 84749 |
rs150220465 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109074949 | TCTAGATTCCATATA[C/G]GTATGAGATCAGGTG | 84749 |
rs150263282 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | USP30 | GRCh38.p7 | 12:109059403 | GTCTTACTATGTTGG[C/G]CAGGCTAGTCTCAAA | 84749 |
rs150316431 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109037166 | ACTATCTTCATGTTC[A/G]TTGATACTTTGCTTA | 84749 |
rs150368293 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP30 | GRCh38.p7 | 12:109041191 | TGTGCTGAAGACTTA[C/T]GGGATTTCTGTTTTA | 84749 |
rs150414633 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP30 | GRCh38.p7 | 12:109078402 | GCACTTCAGTCTGGG[C/T]GACAGAGTGAGACTG | 84749 |
rs150431042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109047486 | GAGGAAAAAATAAAC[A/G]GAAATCTTGTGAGTG | 84749 |
rs150521904 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP30 | GRCh38.p7 | 12:109057326 | ACAGTTATAATTGAG[A/G]TTTATTTTACATTCT | 84749 |
rs150621218 | snp | C/T | 3.29603e-05 | 0.00405944 | missense, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088396 | CCACGGGAATCCTTA[C/T]GCCGGAAGACAAAGT | 84749 |
rs150679747 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB, nc-transcript-variant | USP30, USP30-AS1 | GRCh38.p7 | 12:109052509 | AGCTATTGCTCTCCG[A/G]GGGCAGCTACTTCCG | 84749 |
rs150693719 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109045816 | AGAATCAATAGAACG[C/T]GTGTGTATGTGTGTG | 84749 |
rs150695577 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP30 | GRCh38.p7 | 12:109024133 | CCTCATCAGAAATAC[A/G]GGGATCAATAACCAT | 84749 |
rs150731844 | snp | A/G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109030866 | TGATCCACCTGCCTC[A/G/T]GCCTCCCTAAGTGCT | 84749 |
rs150794169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109060846 | TTTTAGTAGAGACAG[A/G]GTTTCACCAGGCTGC | 84749 |
rs150841677 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP30 | GRCh38.p7 | 12:109038998 | GTTCTTTACATATTC[C/T]GGATACAAGTCTTTG | 84749 |
rs150885378 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP30 | GRCh38.p7 | 12:109027062 | TAGGGCTTCAACATA[C/T]ACATTTGGGGTGGAC | 84749 |
rs150900915 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | USP30 | GRCh38.p7 | 12:109041740 | AAATTATTTTTTTAA[A/G]GAATTTATCATGGCA | 84749 |
rs150911258 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109072487 | CTTGCAAAGGAACTT[A/G]TATTTTGGAAATAGC | 84749 |
rs150941821 | in-del | -/TC | 0.0232847 | 0.105357 | intron-variant | USP30 | GRCh38.p7 | 12:109048993 | GTCTGACCTCTCATC[-/TC]ATTATGGCTGGGAAC | 84749 |
rs150963390 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | USP30 | GRCh38.p7 | 12:109048538 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 84749 |
rs151019398 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109074239 | CAAATAATATTGCAT[C/T]ACATGGATCTACAAC | 84749 |
rs151089144 | snp | A/G | 0.000298686 | 0.0122169 | missense, intron-variant | USP30 | GRCh38.p7 | 12:109057926 | CTGCTTTTTTTTTAG[A/G]GCTTGTGCCTGGCCT | 84749 |
rs151169252 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109064846 | GGGTTAAAGGAGGCA[A/T]TAAAATTTTCCTTTG | 84749 |
rs151175038 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | USP30 | GRCh38.p7 | 12:109077179 | ATGAGGAATATTGTT[C/T]TTACACTTTTCTTCT | 84749 |
rs151228295 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | USP30 | GRCh38.p7 | 12:109025188 | CCCCCTTGGGTTTTT[A/G]GGCCCTTGAATTTGG | 84749 |
rs180675573 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109065199 | TGAACTTCCAGAAAC[C/T]GCACTGAGAGGCAGG | 84749 |
rs180677795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109044173 | AGTAGTTGAATAAAT[A/G]GAGACAAAATGTAGA | 84749 |
rs180690625 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109025205 | GCCCTTGAATTTGGC[C/T]CAGCATCCCAGGGTT | 84749 |
rs180833437 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109035128 | AATGTAAAAAATTAA[A/T]GTAATCACCAATAAT | 84749 |
rs180835502 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109082533 | CACAAATAACTGGGC[A/C]GCTGGGTTCATTTCA | 84749 |
rs180838022 | snp | A/G | 5.12125e-05 | 0.00506 | intron-variant | USP30 | GRCh38.p7 | 12:109073563 | ACACTTGATATTTCC[A/G]GGAGAGGTTTTCCAA | 84749 |
rs180875760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109057073 | TGTTCTCATTAGTAC[A/G]GCAATTGTAGTTTTC | 84749 |
rs180967922 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109060806 | ATTACAGGCATGCCC[C/G]ACCACGCCTGGCTAG | 84749 |
rs180969316 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109038419 | ATTGATGAGCATTTG[A/G]GTTGAATCCATGTCA | 84749 |
rs181014463 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109076794 | TGGAGTGCAGTGGCG[C/T]GATCTCGGCTCACTG | 84749 |
rs181274060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109024499 | GTGAGCTCAAGCAAT[C/T]AACCTGCCTCGGCCT | 84749 |
rs181335788 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055874 | AATTTTATGTTAGAA[A/G]GTGGTTAAGTTCTAT | 84749 |
rs181442677 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109029188 | CTGCAGCTTGGTCCA[A/G]ATGTCTAGCTCTGGA | 84749 |
rs181448309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109072896 | ACTATCCCAATTTTC[C/T]GCACACTGAGGCTTG | 84749 |
rs181461702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109034487 | ATCCCAACGCTTTGG[A/G]AGACTGAGGTGGGAG | 84749 |
rs181469469 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109075595 | AACCTCAAGTGATCC[A/G]CCTGTCTCGGCCTCC | 84749 |
rs181486881 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109037930 | AGTGCTGCACATGTG[A/T]ATGTCCTTCTAGATA | 84749 |
rs181594375 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109068817 | GGAAAAAGAGGTGAA[C/T]ACGTCTGTCCGGTGG | 84749 |
rs181595537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109049648 | AGTGGAACCCCATCT[C/T]TACTAAAAACGCTAA | 84749 |
rs181616096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109060554 | AAAAAAAAAATGTGC[A/G]ACTCGCTGCCAGCGT | 84749 |
rs181704515 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109072070 | AGTTAACCAGTAAGG[A/G]TGAAAATATTCTGGA | 84749 |
rs181717863 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055464 | CTGGAGTGCAGTGGC[A/G]CAATCTGGGCTCACT | 84749 |
rs181724062 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109031902 | TGAGCTCAGGAGTTC[A/C/G]AGACCAGCCCTGACA | 84749 |
rs181850081 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109065388 | TGTCCATTTGTTTAG[G/T]TACTGCCTATGTCAG | 84749 |
rs181861213 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109025620 | CTCATATAGAAATTT[G/T]CCTGTAGATACTAAA | 84749 |
rs181909621 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | USP30 | GRCh38.p7 | 12:109078110 | TAACTTTTTGAGGAA[A/C]CTCCTCCGTACAATT | 84749 |
rs181910615 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109061911 | TGCATCCATAGAAAT[A/T]ATATATTGTAGGTTT | 84749 |
rs181916032 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109039645 | GAGATGGAATCTCAC[C/T]CTGTCACCAGGCTGT | 84749 |
rs182083117 | snp | C/T | 1.75019e-05 | 0.00295815 | intron-variant, synonymous-codon | USP30 | GRCh38.p7 | 12:109083070 | CACACCAGGTGTGTG[C/T]GCGCGAGGAGCCGAT | 84749 |
rs182108784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109044686 | GACAAATTTTATGTT[A/G]TATGTACTTTGCCAC | 84749 |
rs182173906 | snp | A/G | 6.60971e-05 | 0.00574841 | synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088275 | AACCTTCTTTCTCAC[A/G]GGAAGACTGTGGTAC | 84749 |
rs182204837 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109048448 | TGCCAGGGGTTGAAG[G/T]GGGGTGGAGGGGGGT | 84749 |
rs182256674 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109066577 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 84749 |
rs182259144 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109084550 | GGGATGCTGTTCAAC[A/T]TCCTCTAATGCACAG | 84749 |
rs182387941 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109040906 | AACATGGGGGATCAT[G/T]GGGGACATATCTTTG | 84749 |
rs182395653 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022007 | CTGGGATCACAGGCT[C/T]ATCCCAGCATACCCA | 84749 |
rs182449945 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109068255 | CCCAGTGACATACAG[G/T]TGCATCCTCCACAGC | 84749 |
rs182473159 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109028725 | CAGGTGATCCACCCC[C/T]CTCAGCCTCCCAAAG | 84749 |
rs182546603 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109045690 | GCAGTGCATGTAGGT[A/G]CCTAGCATGGGGTCT | 84749 |
rs182569672 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109078930 | TTCTATTGTCTTCTG[A/G]CCTCCATTTTCTCAG | 84749 |
rs182574479 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109063163 | GGAGCGCAGTGGTGC[A/G]ATCTTAGCTCACTGC | 84749 |
rs182678746 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP30 | GRCh38.p7 | 12:109069401 | CACCTCTGGTGTGCC[A/G]TTGGCTAATAGCTAG | 84749 |
rs182697139 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109029525 | GCACCTAAAGGGAAA[A/G]GAATGTACTTATTAG | 84749 |
rs182699761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109083831 | TCCCTTACTCCTTTT[A/G]TTCTTTTTATGACCA | 84749 |
rs182712801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109065611 | CTAACATACAGATGT[A/G]AGATTTGATTGGCTA | 84749 |
rs182718093 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109045217 | TTCCTGACCTCGGGT[A/G]ATCCACCCGCCTCGG | 84749 |
rs182726920 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP30 | GRCh38.p7 | 12:109025888 | AGATGGAGTTTTGCT[C/T]CATTGCCCAGGCCGA | 84749 |
rs182831950 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109026628 | GCGCACCACCATGCC[C/T]ACCTAATTTTTGTAT | 84749 |
rs182841004 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109070486 | AGGAACAGCAAAGAG[G/T]CCAGGGGCCGGGACA | 84749 |
rs182856841 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, downstream-variant-500B | USP30, USP30-AS1 | GRCh38.p7 | 12:109052011 | CCACTTACAAGCTGC[G/T]TCAAAAAACTTACTA | 84749 |
rs182860688 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109030068 | ATACATGTTCACCTT[A/C]TTCCTGCAAGTTACG | 84749 |
rs182964071 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109050358 | TTTTAAGGAAACAAA[A/T]ATTCTCAATTTTAAT | 84749 |
rs182973197 | snp | A/T | 1.65042e-05 | 0.0028726 | missense, intron-variant | USP30 | GRCh38.p7 | 12:109057946 | GTGCCTGGCCTTGTT[A/T]ATTTAGGGAACACCT | 84749 |
rs182983286 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109035435 | GTGGCACAATCTCGG[C/T]TTACTGCAACCTCCG | 84749 |
rs183034184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109058801 | TCAAATGTTCGACTC[A/G]ACCATCATCAAAGAA | 84749 |
rs183153076 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109073960 | GCCATTACTGACTCC[A/G]GGATCAGTCAACTTT | 84749 |
rs183280529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109029629 | CTCCGTGCCTGAGCT[A/G]TCTTATCTGTGTTTT | 84749 |
rs183288690 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP30 | GRCh38.p7 | 12:109074349 | TTTACATACAAGTTT[C/T]TGTGTGGACATATAT | 84749 |
rs183306121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109035789 | TACATCTTTAGGCAT[C/T]GTGTGCCCATCAGCA | 84749 |
rs183371466 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109080254 | ATTCTTGAACTCTGT[C/T]GTCTGACCACTCAAT | 84749 |
rs183386973 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109063761 | TAATTGCTTTAATTT[A/G]CATTTCCCTAATGAT | 84749 |
rs183401414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109078531 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 84749 |
rs183420939 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109040123 | ATTTAAAATATTTAT[A/G]TGCCACAGGTTGATG | 84749 |
rs183563894 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109087509 | CAGCTTGAACTGTAC[A/G]GTCCGTCCTGCACTC | 84749 |
rs183635081 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109062521 | TTTTAGTAGAGACGG[A/G]GTTTCACCGTGTTAG | 84749 |
rs183665403 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | USP30, SVOP | GRCh38.p7 | 12:109021229 | TTGTCCGGGTACCAG[A/T]GAGCACCCTTTGATT | 84749 |
rs183734415 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109066830 | AGAGGAGTGTAGCAC[C/G]AAATATGGGGTTGGA | 84749 |
rs183736591 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109059203 | AACTTTTTTTTGTTT[C/T]TGTTTTTTGAGACAG | 84749 |
rs183742357 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP30 | GRCh38.p7 | 12:109036600 | AGTATTTCTTATAGG[A/G]CAAGTCTGCTAGTGA | 84749 |
rs183752368 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | USP30 | GRCh38.p7 | 12:109027229 | CATTGAGTAATAACT[C/G]CCTGTTCCTCCCTCC | 84749 |
rs183835593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109082190 | TGGACCAAATCTCTT[C/T]CCCAGATGAGTTTTG | 84749 |
rs183849039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109064803 | AGTAGATATTGCCAA[A/G]TTGCCCCATAGTATT | 84749 |
rs183859989 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109043556 | TTGCCCCTTACCTAA[A/C]AACACATACAAAAGT | 84749 |
rs183863002 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109024585 | TTTAAGTATCAACTT[G/T]GTGGGTTTAAGGAAT | 84749 |
rs183924218 | snp | A/T | 1.65625e-05 | 0.00287766 | missense | USP30 | GRCh38.p7 | 12:109084992 | AAACACAGATTTTTA[A/T]GAATGGCGCCTGCTC | 84749 |
rs183926589 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109051070 | CTTTTCTTTGTTTTT[C/T]GGTAGCCATGGGTTC | 84749 |
rs183944550 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046090 | GCTTGGGGGAAGTCA[A/G]TCTTTTTTTTTTTTT | 84749 |
rs183989642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109067319 | AGACGGAGTTTCACC[A/G]TGTTAGCCAGGATGA | 84749 |
rs183992632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109047284 | AGGTCAACCCACAAA[C/T]TTGTCTGGGGAGAAG | 84749 |
rs184003010 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109027572 | GTGAGTGCCACAGTG[C/T]CAGGCCTATTCTACT | 84749 |
rs184074865 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109070265 | TCAGGAATTTAGGGC[A/G]TATTTTGGAGGAGGG | 84749 |
rs184167112 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109085459 | ATTGATACAAACATC[C/T]ACATATACACAATAT | 84749 |
rs184250226 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109047908 | AAAGTGCAGTCTGCA[G/T]GCTCCCTAAGGGTGC | 84749 |
rs184253168 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109074572 | AGGTCCTGTCTAACA[C/T]TGAGGTTCTAGCCAT | 84749 |
rs184389449 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109068050 | CTTAAAGTAGCCCGA[A/C]ACCTCAAGCAGATGT | 84749 |
rs184409130 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP30 | GRCh38.p7 | 12:109028622 | AGCTGAGATTACAGG[C/T]GTGTGCCAACACGCC | 84749 |
rs184446337 | snp | G/T | 0.0190902 | 0.0958158 | intron-variant | USP30 | GRCh38.p7 | 12:109072282 | AAGGTTTTCAGTCTG[G/T]TTTTTTTTTTTCTCC | 84749 |
rs184452336 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055522 | ATTCTGCCTCGGCCT[C/T]CAGAGTAGCTGGGAT | 84749 |
rs184461222 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109032456 | AATGGAATATTATTT[C/G]TCAATAAAAAAGAAA | 84749 |
rs184623501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109071000 | GGTGAAGCTTGAAGA[C/T]GTTATGCCGAGGAAA | 84749 |
rs184633013 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109030930 | ATTGTGATTCTTTTA[A/C]AATGTACACATATAT | 84749 |
rs184758635 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052820 | GGTCCCCAGCTTGGG[C/T]CCGTGACGGCTTTTT | 84749 |
rs184772484 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109074881 | AGCAACATCTCCCCA[C/T]CTCCCCAGCCCCTGG | 84749 |
rs184773921 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | USP30 | GRCh38.p7 | 12:109059616 | CCTCCCGGGTTCAAG[C/T]GATTCTTCTGCTTCA | 84749 |
rs184782180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109037199 | TGTTCAAATCTGCTG[C/T]TGTGCTCGCTAGTGA | 84749 |
rs184921553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109031550 | AAAACGTGAACAACA[A/G]ATGTTCATAGCAGCA | 84749 |
rs184958264 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109060724 | CAGTGGCGGGATCTC[A/G]GCTCACTGCAACCTC | 84749 |
rs184992456 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | USP30 | GRCh38.p7 | 12:109061587 | CTAATTTTTTGTATT[C/T]TGAGTAGAGACAGGG | 84749 |
rs185000566 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | USP30 | GRCh38.p7 | 12:109038985 | TTGAATTGCAAGAGT[G/T]CTTTACATATTCCGG | 84749 |
rs185063295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109076400 | TTCCTTTCCAACCCA[A/G]TCTTTATTCCTTTTT | 84749 |
rs185100424 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP30 | GRCh38.p7 | 12:109080922 | GGTTCTTGTAAGCGC[A/G]CTCTGCGATGTTTAC | 84749 |
rs185108006 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109054285 | CAGCTCTTTGGAAGG[C/T]TGAGGCAGGTGGATT | 84749 |
rs185108616 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109042398 | CCCAGTTACTTATTT[A/T]TCCCTACAATTATAA | 84749 |
rs185170596 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109076877 | GCTGGGACTACAGGC[A/G]CCCGCCACCACGCCC | 84749 |
rs185219474 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109063951 | CATCTCAGCTCACTG[C/T]GACCTCCGCCTCCTG | 84749 |
rs185235850 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109023779 | CTGGGATTACAGGTG[C/T]CCGCCACCATGCCTG | 84749 |
rs185518796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109084358 | ACATGTATGAATGCT[A/G]TTACACGTTGGTATT | 84749 |
rs185522889 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109065714 | TCCAGTCCATTCAGC[C/T]TAGGTTTGAGGGAAG | 84749 |
rs185526838 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP30 | GRCh38.p7 | 12:109045363 | GTGTTAATGAGATCC[C/T]AGCTAAAATCAGGGC | 84749 |
rs185541079 | snp | A/C | | | intron-variant | USP30 | GRCh38.p7 | 12:109026048 | ACCATGTGTATCTTA[A/C]TACCATGATTCTTTT | 84749 |
rs185583924 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022922 | GGCTCCTTCTCACCT[C/T]ATACTGGAGTCAATC | 84749 |
rs185706131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109041682 | ATATATGTGAAGTAT[A/G]AACTTATCAATCATA | 84749 |
rs185854202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109068970 | AGCTAGAGCTTCAGA[A/G]GATGCATTGGGCCAA | 84749 |
rs185871066 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP30 | GRCh38.p7 | 12:109049723 | GGGTGGCTGAGGCAC[A/G]AAAATCGCTTGAACC | 84749 |
rs185877318 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | USP30 | GRCh38.p7 | 12:109029311 | AGAGGGGCTTCTGGC[C/T]GAGTTAGGTCAGAGG | 84749 |
rs186006726 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109025744 | TGGTGTGATCACAGC[C/T]CACTGCAGCCTGGAC | 84749 |
rs186043297 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109050833 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 84749 |
rs186075171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109078357 | TGAACCCAGGAGGCC[A/G]ATGTTGTGGTGAGCC | 84749 |
rs186091223 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109062166 | TCTTGAACTCCTGGG[C/T]TCAGGTGATCCACCC | 84749 |
rs186172219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109069986 | CAGGGCGGGGAGGGC[A/G]GTGGAGGAGAGGGGC | 84749 |
rs186179373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109073019 | CACTTATGTTCTTTC[C/T]ATTAAACCCCATTCT | 84749 |
rs186182915 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | USP30 | GRCh38.p7 | 12:109029526 | CACCTAAAGGGAAAG[A/G]AATGTACTTATTAGG | 84749 |
rs186202475 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109034923 | TCTATTTTGTCTGAT[A/T]TTAGTGTAATTACTT | 84749 |
rs186323806 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109029000 | ATGTATAATTAAAAT[A/G]TTGGCTTGTTGTGGT | 84749 |
rs186344028 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109056540 | CCTGATTTTCAAGAT[A/G]TAATCCTATGACTAT | 84749 |
rs186420657 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109073622 | AGTGGGCTGACATCG[G/T]TCACTGGTGTTAGAG | 84749 |
rs186425035 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109057663 | ACATTTAGGAAGAAC[C/G]AAGCTGTGCTGGATA | 84749 |
rs186428404 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | USP30 | GRCh38.p7 | 12:109035223 | ATTACTGTCTTCTTT[C/T]GTGTTCAATATATAT | 84749 |
rs186432770 | snp | A/G | 3.36519e-05 | 0.00410181 | intron-variant | USP30 | GRCh38.p7 | 12:109082814 | CCCCTGAAACAACTC[A/G]GTTCTCCCGATTTCT | 84749 |
rs186648381 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109044753 | AATAAATATGTTTAT[A/T]CTTCTACATATGTGA | 84749 |
rs186710816 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109078809 | AAATGTTTTTGTCTT[A/G]CCTTCATTTTTGAAG | 84749 |
rs186845872 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109083333 | CAGCTTTGCCTTCTA[A/T]TTTTTCCGCTAAATG | 84749 |
rs186851148 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109079481 | TTATCCTCCCACCTT[A/T]GCCCCCTGAGCAGCT | 84749 |
rs186856968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109063201 | GCCTTCCAGATTCAA[A/G]TGATTCTCCTGCCTC | 84749 |
rs186869448 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109040928 | ATATCTTTGAGGCTA[A/C]CACACTCAGCTTTTC | 84749 |
rs186876917 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109022054 | TAGAGATGGGGTCTT[G/T]CTTTGTTGCCCAGGC | 84749 |
rs187008294 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | USP30 | GRCh38.p7 | 12:109039832 | GCCAGGATGATCTCG[A/G]TCTCTTGACCTCATG | 84749 |
rs187016950 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109068596 | TTAAAATCCTCCTCT[A/G]GTAACTGGAATTATT | 84749 |
rs187067828 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109065567 | AAACGGAGGTACTGA[A/G]CAGAATTATAACATT | 84749 |
rs187146639 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB, nc-transcript-variant | USP30, USP30-AS1 | GRCh38.p7 | 12:109052402 | GCCTAAGCAAATCTG[A/G]AAACCAAGCAGCCCC | 84749 |
rs187148255 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP30 | GRCh38.p7 | 12:109030678 | CTGGAGTGCAGTGGC[A/G]CTATCTTGGCTCACT | 84749 |
rs187236208 | snp | C/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109049286 | ACTCTTCCTATCCCT[C/T]GAACATTTAGAGGCG | 84749 |
rs187389064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109065243 | TTCTCTCACACTCTA[A/G]CAGTACTGGTCTAGT | 84749 |
rs187416402 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109025403 | CCGGAGAGCTCTGAC[C/T]AATACAGTGCTTATC | 84749 |
rs187435460 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109046307 | TTTAGTAGAGACAGC[A/G]TTTCACCATGTTGGC | 84749 |
rs187440149 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | USP30 | GRCh38.p7 | 12:109027492 | GCTATGTAACCCAGG[C/T]TGGTCTCGAACTCCG | 84749 |
rs187440216 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109074011 | TAAAGAAACTCCATA[C/G]TCATTAGCAACCTCT | 84749 |
rs187441606 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109058496 | AGAATCGCTTGAACC[C/T]GGGAGGCGGAGGTTG | 84749 |
rs187545775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109051071 | TTTTCTTTGTTTTTC[A/G]GTAGCCATGGGTTCT | 84749 |
rs187554841 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109029939 | GAGTTCTCCAGCCCT[C/G]CCATAATCCCTCCTC | 84749 |
rs187642498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109052895 | AGGTTCTGCGTCCTT[C/T]AGGGTTGGAGGCCTG | 84749 |
rs187664491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109044525 | GTCTGTAGTCCTAGC[C/T]ACTCGCGAGGCTAGG | 84749 |
rs187792479 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP30 | GRCh38.p7 | 12:109036057 | CCCAGCTAATTGGGA[A/G]GCTGAGGTGGGAGGA | 84749 |
rs187872869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109080255 | TTCTTGAACTCTGTC[A/G]TCTGACCACTCAATC | 84749 |
rs187904157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109071102 | GAGAGATAAAGAATG[A/G]TGGGTGCCAGGGGTT | 84749 |
rs187971155 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109074391 | TTGGGTATATACCTC[A/G]GAGTAGAATTGCTAG | 84749 |
rs187984710 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109078266 | CCGTCTCTACTAAAA[G/T]TACAAAAATTAGCTG | 84749 |
rs188001137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109074731 | TGTGTGCACGTGCAC[C/T]TGTGCTCATATGTGG | 84749 |
rs188014966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109059317 | CTTGTGCCTCAGCCT[C/T]CTGAGTAGCTGGGAT | 84749 |
rs188016504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109036631 | CAAGTCTCTGTTTTT[C/T]TGTTTTGTTTAAGAA | 84749 |
rs188126959 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP30 | GRCh38.p7 | 12:109062570 | CCTGACCTCGTGATC[C/T]GCCCGCCTTGGCCTC | 84749 |
rs188140633 | snp | A/G | | | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109021493 | AATTAGGTATGAGAA[A/G]GCCAAAGATCACTCA | 84749 |
rs188180986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109082433 | ATGACATGCCAGTGT[C/T]AGAGCATCAGTGTTC | 84749 |
rs188185044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109065134 | TTCAAGCCCATTGAC[A/G]GCAAGTCAGAAAGAA | 84749 |
rs188188576 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109043787 | TCAAGAGTAAGAAAG[C/G]AACCCACAGAATAGG | 84749 |
rs188201026 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109024681 | CTGGAGTGCAGTGGC[A/G]CGATCTCAGCTCACT | 84749 |
rs188260190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109058914 | AATACATCCATACAC[C/T]GCTGAGAGGGGTGTA | 84749 |
rs188415207 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | USP30 | GRCh38.p7 | 12:109040683 | GGCAAGTTGGTAATG[G/T]CTGTTGGCAGAAGGC | 84749 |
rs188416495 | snp | A/G | 0.000578211 | 0.0169933 | synonymous-codon | USP30 | GRCh38.p7 | 12:109085038 | AACGCTGTCAGCGCC[A/G]ATGCCCTTCCCTCTC | 84749 |
rs188518733 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109086521 | TTTTCTAATCTTTCA[A/G]TTCTTTCTATGGAGT | 84749 |
rs188526798 | snp | C/T | 0.0008259 | 0.0203044 | intron-variant | USP30 | GRCh38.p7 | 12:109067484 | TGGTTAGTTGTTATG[C/T]TGATGAATTTAATAA | 84749 |
rs188533166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109047378 | AAAAAACAAGAGCTA[C/T]AACAAACAGTTCTGA | 84749 |
rs188537213 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109028203 | CCCTCACTCATTTTT[A/T]AATTGAATTGTTCGG | 84749 |
rs188666750 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109024062 | CTCTTCCCAGCTCCA[A/C]CTCTTCCTGGGTGGG | 84749 |
rs188708542 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109067195 | GTCTGCTCACTGCAA[C/G]CTCCGCCTCCCGGGT | 84749 |
rs188750076 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109035565 | GATGAGGTTTCACCA[C/T]GTTGGCCAGGATGGT | 84749 |
rs188772946 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109042086 | AAGAGGCATATCCTT[A/T]TAGTCATTTTTCTGT | 84749 |
rs188861812 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109023413 | AAAAAAACTTAGCCA[A/G]GTGTGGTGGCACAGA | 84749 |
rs188908647 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109066710 | AAAAGTACACTACTC[A/G]AAAGACCCTTTAGGC | 84749 |
rs188926175 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP30 | GRCh38.p7 | 12:109027018 | GATTACTTCCCAAAG[A/G]CCCCATTTCCAAATA | 84749 |
rs188958733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109072645 | TGAGCTGAATCTGTC[A/G]TGTCCTCAGCATTTC | 84749 |
rs188960975 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055565 | CCACCACACCCAGCT[A/C]ATTTTTGTATTTTTA | 84749 |
rs189071394 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP30 | GRCh38.p7 | 12:109068181 | AGACCGCTGTTACCA[A/G]CAGCAAGTCTGAAGC | 84749 |
rs189087215 | snp | G/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109068688 | ATCAGATAACTTTTT[G/T]AAGGTCCGACTTCTC | 84749 |
rs189091325 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109049479 | CAATAGTAACATTAA[C/G]GATCACTGATCACAG | 84749 |
rs189097851 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109075383 | AGACAGAGTCTCGCT[A/C]TGCTGCACCCAAACT | 84749 |
rs189104041 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP30 | GRCh38.p7 | 12:109029023 | GTTGTGGTCCTTACC[C/T]AATTACAGGGCATCT | 84749 |
rs189188675 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109084584 | AGCCCCCGCAACAAA[A/G]AATGATCCAGCCAAA | 84749 |
rs189196725 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109045998 | AGAGTGTGCCAGAAA[C/G]CTGGAGACCTATGGA | 84749 |
rs189337619 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP30 | GRCh38.p7 | 12:109087551 | ACCTTGACTTTGATG[C/T]TGAAATGAACACACT | 84749 |
rs189440897 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP30, USP30-AS1 | GRCh38.p7 | 12:109055144 | TTGTATAAAAACAAT[A/G]TTTTAAATTGTTGGG | 84749 |
rs189446146 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | USP30 | GRCh38.p7 | 12:109031637 | GATAAACAAAATGTG[G/T]TCTATCCATGCAATG | 84749 |
rs189517650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109030962 | AAATCATCAAGTTGT[A/G]CATCTTAAATATATA | 84749 |
rs189525103 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109076590 | CTTTATCATACTGAC[A/C]AACTTCCCTTCTGTT | 84749 |
rs189537015 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP30 | GRCh38.p7 | 12:109038250 | GTTCTCACCATGCAG[A/C]TCCCAATTGTAAGCA | 84749 |
rs189591164 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109076968 | CGATCTCCTGACCTC[C/G]TGATCCGCCTGCCTC | 84749 |
rs189595592 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109061690 | GCTGGGATTGCGGAC[A/G]TGAGCCACCATGCCT | 84749 |
rs189608690 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | USP30 | GRCh38.p7 | 12:109039199 | CAAAGATTTTTCTCC[A/G]TTTTCCTCAGAAAGT | 84749 |
rs189687778 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109033681 | TAGTCTGCTAGCCAT[C/G]CTGATGGGATGGCAC | 84749 |
rs189703911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109063994 | TTCTCCTGCCTCAGC[C/T]TCCTGAGTAGCTGGG | 84749 |
rs189803889 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109060798 | TAGCTGGGATTACAG[C/G]CATGCCCCACCACGC | 84749 |
rs189850388 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109026573 | CAAGTGATCCTTCCA[A/C/T]CTCAGCCTCCTGAGT | 84749 |
rs189957879 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109042863 | AACCTTAAAGAGTCC[A/C]GAAAAAAGCTGTTAG | 84749 |
rs189987067 | snp | A/G | 0.0001319 | 0.00811989 | synonymous-codon, missense, downstream-variant-500B | ALKBH2, USP30 | GRCh38.p7 | 12:109088425 | GTCTCTGCAGGCACC[A/G]AAGGAGACAGAGGCA | 84749 |
rs190030434 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | USP30 | GRCh38.p7 | 12:109059755 | TGACCTCAACTGATC[G/T]GCCTGCCTCAGCTCA | 84749 |
rs190030925 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109084442 | AACTTGGAGGAGTTT[A/T]GCCTCCCAAGGGACA | 84749 |
rs190039928 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109066540 | AATACAAAAATTAGT[C/T]GGGCATGGTAGCGCA | 84749 |
rs190046148 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP30 | GRCh38.p7 | 12:109045534 | AGAATCACACAGACC[C/T]GCCTGCCATACTGTC | 84749 |
rs190138250 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109081251 | TCTCAATATTAAACT[A/G]TTTCATAGTCACATA | 84749 |
rs190171914 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109040848 | TGGAATTCACATAGC[A/G]TCACTCTCACAATAG | 84749 |
rs190180485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109069035 | TCACAATAACCATGT[A/G]AGGAATTACTGTTGT | 84749 |
rs190186445 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP30, SVOP | GRCh38.p7 | 12:109021582 | ATGAGTAAAATAAAG[C/T]CTCTGCCTTCAAGAT | 84749 |
rs190193464 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109049882 | GTGGTACAGAGACAC[A/G]AAGTGAGCACATGCT | 84749 |
rs190286974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109037856 | GCTTGTGTCAAACAT[C/T]AAGGTCAGCCAGATG | 84749 |
rs190330893 | snp | A/C/T | 4.94811e-05 | 0.00497378 | synonymous-codon, missense | USP30 | GRCh38.p7 | 12:109082909 | GGCACGCCTCTGAAG[A/C/T]GGCATGAGCACGTGC | 84749 |
rs190340073 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109074100 | ATTTGCATATTCTGG[A/T]TGCTTCATATAAATG | 84749 |
rs190345696 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109044576 | CTGGAGTTCAAGGCT[G/T]CAGTGAGCTGTGATA | 84749 |
rs190500535 | snp | C/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109028629 | ATTACAGGCGTGTGC[C/G]AACACGCCTGGCTAA | 84749 |
rs190518004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109044809 | TGTAATTCTGATAAA[C/T]ATCCAAATTGCTCTA | 84749 |
rs190526107 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109025836 | AGGACTACAAGTGTG[A/C]ACCACCACACCTGGC | 84749 |
rs190582128 | snp | A/T | | | intron-variant | USP30 | GRCh38.p7 | 12:109065323 | GGCTCATGGGCCAAA[A/T]CCAGCCCACCACCTG | 84749 |
rs190601439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109025483 | CTACCTTAAAATGTT[A/G]GCTGGCCTATGAAGG | 84749 |
rs190635318 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP30 | GRCh38.p7 | 12:109070055 | GAGGCTGCGGGCGGC[A/T]TCAGCTTCTATTGTG | 84749 |
rs190657743 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP30 | GRCh38.p7 | 12:109029619 | TCCACCCTCCCTCCG[A/T]GCCTGAGCTATCTTA | 84749 |
rs190678246 | snp | A/G | | | intron-variant | USP30 | GRCh38.p7 | 12:109070450 | GCACAGCCCGAAATG[A/G]GAATAAGCTGGATAT | 84749 |
rs190736565 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109047978 | CATAATAATACTAAG[A/C]CCTTCCCATTCCCAT | 84749 |
rs190788900 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP30 | GRCh38.p7 | 12:109057033 | TTGTAATGAAAAATG[C/T]CAAGCGGCATAATTG | 84749 |
rs190813221 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP30 | GRCh38.p7 | 12:109073779 | GAGTCCAGTGGTTGA[C/G]TCTATGCTCATGGTG | 84749 |