SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs7655 | snp | A/G | 0.113685 | 0.209567 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066377 | CTGGGAGGCTAAAGC[A/G]CTCATGTCCTGGCTC | 219333 |
rs9901 | snp | A/T | 0.495213 | 0.048687 | intron-variant | USP12 | GRCh38.p7 | 13:27072462 | GATGCCTAAGAAACA[A/T]CTTCCTTAGGTGGAA | 219333 |
rs472339 | snp | A/T | 0.135143 | 0.222054 | intron-variant | USP12 | GRCh38.p7 | 13:27109383 | actaaactttaatca[A/T]gtctctacgtgtaac | 219333 |
rs479920 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | USP12 | GRCh38.p7 | 13:27106790 | AATGGAGAGATGGAT[A/G]AAAATGAGACTTCTC | 219333 |
rs480523 | snp | A/G | 0.192401 | 0.243274 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136911 | AACATTGGTCAAGAG[A/G]TGTTTTTTGCGTTAA | 219333 |
rs488119 | snp | A/T | 0.339203 | 0.233544 | intron-variant | USP12 | GRCh38.p7 | 13:27104633 | TGTGTATGTGGGGAA[A/T]ATGAACAAATCTTCA | 219333 |
rs488218 | snp | C/T | 0.185155 | 0.241444 | intron-variant | USP12 | GRCh38.p7 | 13:27104654 | CAAATCTTCAACAAA[C/T]GTATCAAATTCAAGA | 219333 |
rs494649 | snp | C/T | 0.212425 | 0.24716 | intron-variant | USP12 | GRCh38.p7 | 13:27090841 | TGTGCTAATAATAAT[C/T]TTGATGTATTAAAAT | 219333 |
rs497224 | snp | A/T | 0.0941369 | 0.195465 | intron-variant | USP12 | GRCh38.p7 | 13:27085190 | gcgagactccatctc[A/T]aaaaaaaaagaaaga | 219333 |
rs497329 | snp | G/T | 0.0372196 | 0.131242 | intron-variant | USP12 | GRCh38.p7 | 13:27111518 | CCCTACTCGAGGTCT[G/T]ATCATTGATTTTTTG | 219333 |
rs505361 | snp | C/T | 0.177824 | 0.239355 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166245 | TTCTCTTTTAGCAGC[C/T]CTATTCCAGAAACTT | 219333 |
rs507243 | snp | C/T | 0.107694 | 0.205546 | intron-variant | USP12 | GRCh38.p7 | 13:27102275 | TTTCTTCCAAAATAA[C/T]AGTAGATCACCCACA | 219333 |
rs507580 | snp | C/T | 0.109461 | 0.206758 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127725 | GTGCTTCTGTGGTGG[C/T]AGTTGAAGGAGAAAG | 219333 |
rs514128 | snp | C/T | 0.166832 | 0.235761 | intron-variant | USP12 | GRCh38.p7 | 13:27119943 | ATTCAAGGTTTTCCT[C/T]AACAGAAATGATCAG | 219333 |
rs515025 | snp | A/G | 0.0839998 | 0.186933 | intron-variant | USP12 | GRCh38.p7 | 13:27071402 | CAGTAAAAAATTTCA[A/G]TAATATAGCTGTATG | 219333 |
rs520344 | snp | C/T | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27102315 | TGTAAAGAGAGGACT[C/T]catttcctacctggg | 219333 |
rs521995 | snp | C/T | 0.0748431 | 0.178382 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133167 | CAAAAATATCTGATC[C/T]ATTAATAACACAGTC | 219333 |
rs522268 | snp | C/T | 0.363985 | 0.222503 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164356 | ACGTAGCTTTGGACA[C/T]GTGGCTCACTACAGA | 219333 |
rs526413 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135450 | gggcatgctggctca[C/T]gcctataatcccagc | 219333 |
rs532341 | snp | G/T | 0.151668 | 0.229849 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27123915 | CTTGAAAAGATGAGG[G/T]CTTGTCCTTTTCACA | 219333 |
rs534542 | snp | C/G | 0.0494327 | 0.149241 | intron-variant | USP12 | GRCh38.p7 | 13:27102939 | ACATGCATGGAGCCA[C/G]TGTTGCTGTACTCTA | 219333 |
rs535947 | snp | C/T | 0.156319 | 0.231784 | intron-variant | USP12 | GRCh38.p7 | 13:27119060 | actataacagaattt[C/T]aacttttctaaggca | 219333 |
rs538344 | snp | C/T | 0 | 0 | synonymous-codon, utr-variant-5-prime, intron-variant | USP12 | GRCh38.p7 | 13:27105735 | AGTAGAATTACCATT[C/T]TCTTTCCGTAATCTT | 219333 |
rs538364 | snp | A/G | 0 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159155 | CTTCTAAAATTGCAA[A/G]ATTAAAAGAAACTAC | 219333 |
rs556647 | snp | A/C/T | 0 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146586 | ACCACTGCAGAGCTC[A/C/T]GATGTTGGCTTATAA | 219333 |
rs563184 | snp | A/T | 0.0475351 | 0.146656 | intron-variant | USP12 | GRCh38.p7 | 13:27093819 | aacatttccactgta[A/T]ggatgtgctgcagtt | 219333 |
rs565596 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | USP12 | GRCh38.p7 | 13:27106383 | TACTCCTCTCCACTC[C/T]AGTAATTGGGGCGAG | 219333 |
rs565707 | snp | A/C | 0.437542 | 0.165312 | intron-variant | USP12 | GRCh38.p7 | 13:27106427 | CGGGCGGGGAAATAA[A/C]CCTACTTTATAAAGT | 219333 |
rs568500 | snp | A/T | 0.17461 | 0.238362 | intron-variant | USP12 | GRCh38.p7 | 13:27106712 | ACCATTTATTTTTTT[A/T]AAAAAAATGAGGAAG | 219333 |
rs570248 | snp | A/T | 0.106987 | 0.205054 | intron-variant | USP12 | GRCh38.p7 | 13:27103878 | TATAAAGCCATAAGT[A/T]TGTAACTGTATTTTA | 219333 |
rs571789 | snp | C/G | 0.0498117 | 0.149749 | intron-variant | USP12 | GRCh38.p7 | 13:27109895 | ccagcctgggcgaca[C/G]agtgagactctgtct | 219333 |
rs766870 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27121137 | TGGGATTATTACTGG[G/T]TCCCTTATGCATTGA | 219333 |
rs832777 | snp | A/T | 0.109461 | 0.206758 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128042 | GTATTTTCAATGAAA[A/T]GTTTCACCACATAAT | 219333 |
rs832778 | snp | A/C | 0.290977 | 0.246619 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130539 | GTTCTCACACACACA[A/C]AAAAAAAATCACAAA | 219333 |
rs832779 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | USP12 | GRCh38.p7 | 13:27087174 | CTGACTTCCTGCCCC[C/T]GCTCCCTGAATGcac | 219333 |
rs832780 | snp | A/C | 0.0372196 | 0.131242 | intron-variant | USP12 | GRCh38.p7 | 13:27085558 | AAGTTTATAGTTCTC[A/C]GTCTTGGAATAATAG | 219333 |
rs865574 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27087098 | cacacacacacacaG[C/G/T]CCCTTCCCCTCTGCT | 219333 |
rs866227 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27087165 | TGCCCCTGCTCCCTG[A/T]ATGcacacacatgca | 219333 |
rs866228 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27086667 | CAAAAGCCACCCTTT[C/T]CCTAGAATGATGGTT | 219333 |
rs953529 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | USP12 | GRCh38.p7 | 13:27112499 | ACTCTGTTGCCCAGG[C/T]TGGTCTCAGATTTCT | 219333 |
rs970449 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167122 | ggcatgtgccaccac[C/G]cccagctaatttttg | 219333 |
rs995424 | snp | C/T | 0.447032 | 0.153878 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145389 | TGTTTCCATGGAACA[C/T]GAATAACAAGCTCCC | 219333 |
rs995425 | snp | A/G | 0 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145544 | CCTAAACTCAAACTA[A/G]CTCCCACATTAACTT | 219333 |
rs1159036 | snp | A/T | 0.387832 | 0.208572 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132979 | GCAACACAGCCATGC[A/T]CCTACTATGAACTGT | 219333 |
rs1170032 | snp | G/T | 0.0836354 | 0.186609 | intron-variant | USP12 | GRCh38.p7 | 13:27078477 | GAATACAACATGGAT[G/T]CAGTTTGTCATTTTA | 219333 |
rs1170035 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137508 | TGCTGTAAATAGATA[A/G]ATGTATACTTAAATG | 219333 |
rs1170036 | snp | G/T | 0.345482 | 0.231048 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137580 | AATAATCATAAGTAA[G/T]ATACCACACTGATTA | 219333 |
rs1170037 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137726 | gcctcccctggaata[C/T]gggcaggacctgtga | 219333 |
rs1170038 | snp | C/T | 0.339203 | 0.233544 | intron-variant | USP12 | GRCh38.p7 | 13:27100631 | CAATCCCGTACAATT[C/T]AAGAACCTTTATCTC | 219333 |
rs1170039 | snp | A/G | 0.029116 | 0.117091 | intron-variant | USP12 | GRCh38.p7 | 13:27107096 | ttgggaggccgaggc[A/G]ggcggatcacttgag | 219333 |
rs1180172 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166110 | TGGGAAAGTTTCTTA[A/T]AACTTCGAGTTAATT | 219333 |
rs1186393 | snp | A/T | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27100541 | ATGGCCTGATTCAGT[A/T]TCTCTCTCCACTTTG | 219333 |
rs1318659 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130448 | atggatgactgcaag[C/T]ctcaaaaaagcaatc | 219333 |
rs1327306 | snp | A/G | 0.291235 | 0.246576 | intron-variant | USP12 | GRCh38.p7 | 13:27096146 | GTTGAAATATTTGTG[A/G]AATAATAAGTCAGGT | 219333 |
rs1327307 | snp | C/G | 0.386313 | 0.209568 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128093 | GAGAATATTTAGAGA[C/G]AACAAAAGAAGATTC | 219333 |
rs1473758 | snp | A/G | 0.121022 | 0.21416 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124886 | AATCAAAGGCAATGA[A/G]AATATTTATGACAAA | 219333 |
rs1547189 | snp | A/G | 0.391024 | 0.206427 | intron-variant | USP12 | GRCh38.p7 | 13:27091268 | TTACATGTAAATTCC[A/G]GCCTGATCTGGCTAG | 219333 |
rs1555976 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27121083 | GGGAGGACAACAGGA[A/G]AGATGAGCATGAAGC | 219333 |
rs1629464 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27093884 | ccttaaaaagacatg[G/T]aagaaccttaaatgc | 219333 |
rs1751773 | snp | C/T | 0.154329 | 0.23097 | intron-variant | USP12 | GRCh38.p7 | 13:27123267 | gtaacaaatcattct[C/T]tccagacctcagttt | 219333 |
rs1762075 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158523 | tcaaacctagatggt[A/G]cagcccactacacac | 219333 |
rs1762079 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | USP12 | GRCh38.p7 | 13:27113703 | GCCCCTAAAACAGGG[C/T]TGGACGCTTGGTACA | 219333 |
rs1960195 | snp | A/G | 0.335101 | 0.23507 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139632 | CAGAAATAAAAATAT[A/G]GTCACTCTTGTATAA | 219333 |
rs1999667 | snp | C/G | 0.0360663 | 0.129354 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164368 | ACACGTGGCTCACTA[C/G]AGATAAATAAAGCAA | 219333 |
rs2104580 | snp | A/G | 0.115788 | 0.21092 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167830 | GGAAAGCTGGGGCAA[A/G]CCTCAGAGCCCATGC | 219333 |
rs2148755 | snp | C/T | 0.0785177 | 0.181917 | intron-variant | USP12 | GRCh38.p7 | 13:27072338 | GTAAGGACTGGTAAA[C/T]TGAAAAAAGTTAGGC | 219333 |
rs2182669 | snp | C/T | 0.0310518 | 0.120672 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173803 | actgggattgtgcca[C/T]tgcaccccagcctgg | 219333 |
rs2478922 | snp | G/T | 0.111224 | 0.207945 | intron-variant | USP12 | GRCh38.p7 | 13:27096520 | GCTTTACCCTGTGCT[G/T]GGCAATATACAACTC | 219333 |
rs2478929 | snp | A/G | 0.0839998 | 0.186933 | intron-variant | USP12 | GRCh38.p7 | 13:27079399 | ACCTGTCAGTGACTG[A/G]TCAAAGACTTGGAAT | 219333 |
rs2484110 | snp | C/T | 0.499587 | 0.0143711 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155332 | GTGATCTGCCCGCCT[C/T]GGCCTCCCAAGGTGC | 219333 |
rs2484111 | snp | C/T | 0.321769 | 0.239477 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158833 | GAAGATCATGGGAAA[C/T]TAAAATGCACACAAG | 219333 |
rs2484112 | snp | C/T | 0.188 | 0.24219 | intron-variant | USP12 | GRCh38.p7 | 13:27069509 | TGGAACTCTCACACA[C/T]AGCTGGCAGGGCACA | 219333 |
rs2484113 | snp | C/T | 0.0839998 | 0.186933 | intron-variant | USP12 | GRCh38.p7 | 13:27070416 | gtgtgtgagtatgGC[C/T]ATTTTATTCTTTTTT | 219333 |
rs2484114 | snp | G/T | 0.29046 | 0.246704 | intron-variant | USP12 | GRCh38.p7 | 13:27074878 | CTCAGAAGTGATTTA[G/T]TTTAACCAACAACCC | 219333 |
rs2484115 | snp | A/T | 0.110167 | 0.207236 | intron-variant | USP12 | GRCh38.p7 | 13:27096990 | GTATTAGAAATCTTT[A/T]AAAAAGTTTTAAAAA | 219333 |
rs2484116 | snp | C/T | 0.170733 | 0.237101 | intron-variant | USP12 | GRCh38.p7 | 13:27112716 | GATGCCATCAACCCT[C/T]TGACATCATGGAACT | 219333 |
rs2497960 | snp | C/T | 0.0865458 | 0.189163 | intron-variant | USP12 | GRCh38.p7 | 13:27115542 | GCAGGTGTTTTAAAA[C/T]GCATATATTGATAAA | 219333 |
rs2497961 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | USP12 | GRCh38.p7 | 13:27097078 | CCATTTATAAGATTG[C/T]CCAGTTTGGTTTTCT | 219333 |
rs2497962 | snp | A/G | 0.139225 | 0.224118 | intron-variant | USP12 | GRCh38.p7 | 13:27096624 | TCTCGTCCCATTTTC[A/G]TGTTTACAAATAAAG | 219333 |
rs2497966 | snp | C/T | 0.089084 | 0.191327 | intron-variant | USP12 | GRCh38.p7 | 13:27079658 | CAATAGTCAGAAACG[C/T]TTTTTAAAGTAAATT | 219333 |
rs2497970 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152351 | tgaaccttgaaaaca[C/T]gcaaagtaaaagcag | 219333 |
rs2497971 | snp | C/T | 0.316243 | 0.241064 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155233 | actacaggcgcgtgc[C/T]accatgcccggctaa | 219333 |
rs2497980 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147616 | TTTGTCTTTGACTTT[C/T]AGCATTTTTATTATC | 219333 |
rs2497981 | snp | C/T | 0.167158 | 0.235875 | intron-variant | USP12 | GRCh38.p7 | 13:27121172 | AAGTCAAGCAAGTTA[C/T]CTTGCTGTTTCTTGT | 219333 |
rs2986635 | snp | C/T | 0.0659589 | 0.169201 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142389 | ATGCATGATCATCTT[C/T]GATACTGGGCATTAC | 219333 |
rs3002289 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | USP12 | GRCh38.p7 | 13:27097398 | ggctcactgcaacct[C/G]tacctcccgggttca | 219333 |
rs3002291 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | USP12 | GRCh38.p7 | 13:27084009 | agctgagattacagg[C/T]gcctgccaccatgcc | 219333 |
rs3187469 | snp | A/G | 0 | 0 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066242 | tgtggggattaatta[A/G]agataatgtctgtaa | 219333 |
rs3858763 | snp | C/T | 0.269267 | 0.249256 | intron-variant | USP12 | GRCh38.p7 | 13:27121237 | GGAGAAACATCTTCC[C/T]AAAATTCATAACCAT | 219333 |
rs4238199 | snp | A/G | 0.463018 | 0.130857 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154600 | CAAAATTCATTAAAG[A/G]CATATCAGGAATTGA | 219333 |
rs4597174 | snp | A/G | 0.0887219 | 0.191022 | intron-variant | USP12 | GRCh38.p7 | 13:27120345 | GGATAAAGAGAAGGC[A/G]TGATGGTGAGTTAAG | 219333 |
rs4769540 | snp | A/C | 0.494057 | 0.0541878 | intron-variant | USP12 | GRCh38.p7 | 13:27094551 | cttgactgggtgatc[A/C]aaaattaatttcacc | 219333 |
rs4769541 | snp | A/G | 0.396909 | 0.202282 | intron-variant | USP12 | GRCh38.p7 | 13:27099194 | GATTGAGGAGCTGGG[A/G]AGGAAGCAGAGAGCA | 219333 |
rs4769542 | snp | A/G | 0.490997 | 0.0664859 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166441 | AAGGAGGCAGACTCA[A/G]TTTGGGGGGACTTGG | 219333 |
rs4771069 | snp | A/T | 0.294064 | 0.246086 | intron-variant | USP12 | GRCh38.p7 | 13:27072893 | CTTTCATATGAAGCA[A/T]ATCTACAAATAAGTC | 219333 |
rs4771070 | snp | C/T | 0.476052 | 0.106772 | intron-variant | USP12 | GRCh38.p7 | 13:27078154 | ACTTGGCCCTCCATA[C/T]TGGGAGTTCCACATC | 219333 |
rs4771071 | snp | G/T | 0.290977 | 0.246619 | intron-variant | USP12 | GRCh38.p7 | 13:27092807 | GGACCTTTAGTTTAT[G/T]GATGACTTTTTAGAT | 219333 |
rs4771073 | snp | A/G | 0.376791 | 0.215463 | intron-variant | USP12 | GRCh38.p7 | 13:27119690 | TACTGTTTTAACACA[A/G]AACTCCAGGGAAGTC | 219333 |
rs4771074 | snp | A/G | 0.44651 | 0.154543 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152959 | aaaaaaaaaaaaaaa[A/G]gaaagaaagaaaAGA | 219333 |
rs5802410 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27103607 | AACTATCAAAAAAAA[A/T]AATAATAATAATAAT | 219333 |
rs5802411 | snp | A/T | 0.368324 | 0.220226 | intron-variant | USP12 | GRCh38.p7 | 13:27114770 | CTCCTCTCCATTTTT[A/T]AAAAAAAAAAAAAAA | 219333 |
rs5802412 | in-del | -/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27114901 | GCTAAGGCAGGATTG[-/C]CTGAGCCCAGGAGGT | 219333 |
rs5802413 | in-del | -/A | 0.498714 | 0.0253268 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130576 | ATCACAAAACATGCC[-/A]AAAAAAAAAAAAAAG | 219333 |
rs6491185 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158115 | gaaatagggtcttta[C/T]agaagtaatcaagtt | 219333 |
rs7318227 | snp | A/T | 0.4444 | 0.15719 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166993 | ATAATCATTCGTGGG[A/T]AAACAGTGTAAAACT | 219333 |
rs7318594 | snp | A/T | 0.0644693 | 0.167566 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150520 | ggcaatactccacaa[A/T]ctgatctacaggctc | 219333 |
rs7318807 | snp | A/T | 0.130351 | 0.219509 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167273 | gtctcaaaaaaaaaa[A/T]aaaataaataaataa | 219333 |
rs7320132 | snp | A/G | 0.494442 | 0.0524218 | intron-variant | USP12 | GRCh38.p7 | 13:27118878 | TTCTAACCACCCCAC[A/G]TGTCCACCTGTCACC | 219333 |
rs7320316 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136951 | GATAGGTGCTTGGGG[A/G]TACATAATACTATTT | 219333 |
rs7320806 | snp | A/C | 0.136847 | 0.222927 | intron-variant | USP12 | GRCh38.p7 | 13:27110792 | TTTGTACTACAATCT[A/C]ATCAAGCTAACGACC | 219333 |
rs7323545 | snp | C/G | 0 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132635 | CTCTGCATTTGCGTA[C/G]GTCTGGCTGTCCTAA | 219333 |
rs7326966 | snp | A/C | 0.41141 | 0.19091 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141676 | ctactctaaaaaata[A/C]atgaatagacagaaa | 219333 |
rs7328829 | snp | A/T | 0.38821 | 0.208322 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137956 | gggcagctgccaact[A/T]ggaaccagaaaaagc | 219333 |
rs7329031 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | USP12 | GRCh38.p7 | 13:27123436 | AAGTCCTGAATGAGT[C/T]AGGAAATAGCATCAT | 219333 |
rs7331742 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141625 | tatcaaaatcaataa[C/T]aataatgagtcacat | 219333 |
rs7331893 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154948 | aaggcaagggcagca[A/T]ccaggtggcaaaggc | 219333 |
rs7331930 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | USP12 | GRCh38.p7 | 13:27103734 | gcaacataatgagac[A/C]ccatctctaccaaaa | 219333 |
rs7333276 | snp | A/G | 0.0799831 | 0.183287 | intron-variant | USP12 | GRCh38.p7 | 13:27170230 | TCTTTAATACTGTCG[A/G]TTTTATGTCCACCTG | 219333 |
rs7333284 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | USP12 | GRCh38.p7 | 13:27070244 | ttatattcaagccta[A/G]gcaaaattaatcata | 219333 |
rs7333910 | snp | A/G | 0.176219 | 0.238865 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170542 | ATAAGCTCATGAGGA[A/G]CTAATGAAACGAATT | 219333 |
rs7334936 | snp | A/G | 0 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167305 | TAACATATCCTCTGG[A/G]AGGTAAAAATTGACC | 219333 |
rs7337059 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167283 | aaaaataaaataaat[A/G]aataaaTAACATATC | 219333 |
rs7337470 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | USP12 | GRCh38.p7 | 13:27103589 | AAGAATTAGTAACTA[C/T]TGAACTATCAAAAAA | 219333 |
rs7337844 | snp | C/T | 0.463666 | 0.129795 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146425 | GCACCTATGTAATAA[C/T]GCACACGGCTAAAGG | 219333 |
rs7338343 | snp | A/G | 0.464203 | 0.128908 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146300 | CCAGCTACTCGGGAG[A/G]CTGAGGCAGGAGAAT | 219333 |
rs7338356 | snp | G/T | 0.0919752 | 0.193722 | intron-variant | USP12 | GRCh38.p7 | 13:27096805 | ACCTATTTAGGACAT[G/T]TTATTTTTAGATCCT | 219333 |
rs7338782 | snp | C/T | 0.030278 | 0.119257 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136088 | TACAATAAAGTAAAC[C/T]GCTTTCCATGTTCTG | 219333 |
rs7981803 | snp | C/T | 0.494896 | 0.0502606 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158362 | ccaaccctgtcgaca[C/T]cctgattctggactt | 219333 |
rs7982139 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131430 | GAAAGTGCTGTAAAA[C/T]GTAAAGCATTATGTA | 219333 |
rs7982273 | snp | C/T | 0.490343 | 0.0688145 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165841 | GAAATTCTTGCTTAA[C/T]TATGTCTGATTCTAT | 219333 |
rs7984452 | snp | A/G | 0.00953873 | 0.0683987 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068387 | AAATATTTAGCCAGA[A/G]ATATCAGTTCCTCCT | 219333 |
rs7984570 | snp | A/G | 0.495016 | 0.0496707 | intron-variant | USP12 | GRCh38.p7 | 13:27075722 | TAAGGCTAAATGCAC[A/G]GGGTGCTCAAGAGTG | 219333 |
rs7984685 | snp | C/T | 0.491732 | 0.0637633 | intron-variant, nc-transcript-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162894 | AAATGTCTGCTGCTA[C/T]GGAAGCAAGAAAATT | 219333 |
rs7985407 | snp | C/G | 0.489665 | 0.0711382 | intron-variant | USP12 | GRCh38.p7 | 13:27083946 | ctcggctcactgcaa[C/G]ctctgcctcccaggt | 219333 |
rs7991877 | snp | C/G | 0.415399 | 0.187465 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173661 | cagcctggccaacgt[C/G]gtgaaatcccgtctc | 219333 |
rs7993065 | snp | A/G | 0.479014 | 0.100263 | intron-variant | USP12 | GRCh38.p7 | 13:27087588 | cactaagcgggctca[A/G]gaacaatgacatccc | 219333 |
rs7993700 | snp | C/G | 0.293807 | 0.246132 | intron-variant | USP12 | GRCh38.p7 | 13:27073530 | AATTTTAAAAGGGGA[C/G]AGTGGGGAGGGGACC | 219333 |
rs7997088 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | USP12 | GRCh38.p7 | 13:27115058 | ACCAACCTTTAATAG[C/T]TGGAGCTGTGGCCCC | 219333 |
rs7997373 | snp | C/T | 0 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138034 | gcaccctaagtgagc[C/T]tgaaagcagatccat | 219333 |
rs7997453 | snp | C/T | 0.447032 | 0.153878 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164508 | CACCTCACACAGTGG[C/T]GCTCTACATTAAATT | 219333 |
rs7998347 | snp | C/T | 0.49089 | 0.0668743 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165506 | AATCATGTTAAAGGG[C/T]AGTAACAGCCAACAT | 219333 |
rs7998437 | snp | A/C | 0.49681 | 0.0398085 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158347 | agccctcagagggaa[A/C]caaccctgtcgacat | 219333 |
rs7998459 | snp | C/T | 0.376791 | 0.215463 | intron-variant | USP12 | GRCh38.p7 | 13:27115748 | CTGGGATGTGCTTTT[C/T]CCCCACATTTCACAC | 219333 |
rs8001868 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130915 | AAATTCCACCACTTT[C/G]CTTCAGCAAGCCGTG | 219333 |
rs8002642 | snp | A/C | 0.0883596 | 0.190715 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171130 | GCTCGGCGCGCGACC[A/C]GAAGGAAATGGAgcc | 219333 |
rs9319340 | snp | C/T | 0.463881 | 0.12944 | intron-variant | USP12 | GRCh38.p7 | 13:27080939 | tctgctggtggaggg[C/T]cttgcctcaaggatg | 219333 |
rs9319341 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27103761 | AAAAAAAAAAAAAAA[A/G]AGAGAGAGAGACAGA | 219333 |
rs9319342 | in-del | -/TAA/TAAA/TAAAA/TAAAAA | 0.464629 | 0.128197 | intron-variant | USP12 | GRCh38.p7 | 13:27110127 | TTTCCTTTTCCAGGT[-/TAA/TAAA/TAAAA/TAAAAA]AAAAAAAAAAAAAAA | 219333 |
rs9507838 | snp | A/G | 0.0887219 | 0.191022 | intron-variant | USP12 | GRCh38.p7 | 13:27081075 | ctggagtgcagtggc[A/G]cgatcttggctcact | 219333 |
rs9507839 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27086274 | atatacatacacata[C/T]atataATTacacaca | 219333 |
rs9507840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27094480 | gcactaaagcctggg[C/T]gacagagcaagaacc | 219333 |
rs9507841 | snp | A/C | 0.396727 | 0.202413 | intron-variant | USP12 | GRCh38.p7 | 13:27097540 | AAAGGGAATGAGTGA[A/C]GCTTTTTATGGGGGT | 219333 |
rs9507842 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | USP12 | GRCh38.p7 | 13:27097550 | AGTGAAGCTTTTTAT[A/G]GGGGTAGGagggcac | 219333 |
rs9507845 | snp | A/G | 0.492823 | 0.0594727 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144911 | CCAAAAAAAGAAAAA[A/G]AAAAAATCAGCCAGG | 219333 |
rs9507846 | snp | C/T | 0.49306 | 0.0584955 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151562 | ctaggcaagaggatc[C/T]cgagggccaggagtt | 219333 |
rs9507847 | snp | A/G | 0.495135 | 0.0490805 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155272 | atttttagtagagac[A/G]gggtttcaccatgtt | 219333 |
rs9507851 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171750 | accccgagccgccgc[C/G]GACCCAACCACCGAG | 219333 |
rs9512533 | snp | C/T | 0.482831 | 0.0910472 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067556 | TTCTCCCAGAACATC[C/T]GTTTAAGCAGCCCAA | 219333 |
rs9512534 | snp | C/T | 0.493613 | 0.0561475 | intron-variant | USP12 | GRCh38.p7 | 13:27069460 | aatttaaaagactga[C/T]aataccaagtatttg | 219333 |
rs9512535 | snp | G/T | 0.496416 | 0.0421803 | intron-variant | USP12 | GRCh38.p7 | 13:27077165 | GACATAAGAAAATAC[G/T]TAAGAAGTCAGGATA | 219333 |
rs9512536 | snp | C/G | 0.391583 | 0.206044 | intron-variant | USP12 | GRCh38.p7 | 13:27077329 | AAAGAAGAATTTTCT[C/G]AGCATAAAATGAGTG | 219333 |
rs9512538 | snp | A/C | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27078579 | gatgggaaaagacat[A/C]ccatgtaaacactaa | 219333 |
rs9512539 | snp | C/G | 0.475525 | 0.107882 | intron-variant | USP12 | GRCh38.p7 | 13:27079268 | GTAAGGATTCAATCT[C/G]AAGCAAAATCCCAGG | 219333 |
rs9512540 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27085180 | tttctttctttcttt[C/T]ttttttttttgagat | 219333 |
rs9512541 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27086268 | atatacatatacata[C/T]acatatatataATTa | 219333 |
rs9512542 | snp | G/T | 0.48546 | 0.0840147 | intron-variant | USP12 | GRCh38.p7 | 13:27086933 | ATTACCAAAAACACT[G/T]TCCTTCCTAGGAAAT | 219333 |
rs9512547 | snp | G/T | 0.376256 | 0.215776 | intron-variant | USP12 | GRCh38.p7 | 13:27102011 | GTATTTCCCATTTTT[G/T]AATGAATGAATGAAT | 219333 |
rs9512548 | snp | C/T | 0.5 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27102018 | CCATTTTTTAATGAA[C/T]GAATGAATGAATGAA | 219333 |
rs9512549 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27106629 | ATCAAGTATATACAG[G/T]ATTAGGTTAAAAAGG | 219333 |
rs9512550 | snp | C/T | 0.394721 | 0.203852 | intron-variant | USP12 | GRCh38.p7 | 13:27108154 | tccaacaatgataga[C/T]tggattaagaaaatg | 219333 |
rs9512551 | snp | G/T | 0.312104 | 0.242163 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131560 | CTTGTTCAAGTACAC[G/T]TGGTTTTGAAAGCCA | 219333 |
rs9512555 | snp | A/G | 0.494568 | 0.0518327 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144883 | CGGGTAATAGGGCCA[A/G]ATCCTGTCTCTACCA | 219333 |
rs9512556 | snp | A/G | 0.443195 | 0.158668 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147801 | tcaaccaacaatgct[A/G]aatctgccaatgctt | 219333 |
rs9512557 | snp | A/G | 0.441158 | 0.161117 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150984 | gcaaaggattgacac[A/G]ggatttggcaaagga | 219333 |
rs9512558 | snp | A/G | 0.081446 | 0.184634 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151882 | atacacaaatggcca[A/G]taagtacctaaagag | 219333 |
rs9512560 | snp | G/T | 0.464203 | 0.128908 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157657 | TTTAATCACTTAACC[G/T]TATTTCTCTCTTGTT | 219333 |
rs9512561 | snp | A/T | 0.465683 | 0.126415 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159550 | GCAGAGGGCCTTGTT[A/T]ACTTGGATGTCAACC | 219333 |
rs9512562 | snp | A/G | 0.499902 | 0.00698814 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159777 | GCTAAAATTACAGAT[A/G]TCACATTCAACTTTA | 219333 |
rs9512563 | snp | A/T | 0.299664 | 0.245017 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161909 | AAAATAAAAAAAAAT[A/T]AAAAAGCCACTCATT | 219333 |
rs9512564 | snp | A/T | 0.494315 | 0.0530107 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163105 | AAAAAAATACAAGCA[A/T]ATTTTGAAAAATCAA | 219333 |
rs9512567 | snp | C/T | 0.404907 | 0.196224 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173183 | GGAAGCCAAGAGCCC[C/T]GATACCCCAGCCAGG | 219333 |
rs9551353 | snp | C/T | 0.172674 | 0.237741 | downstream-variant-500B | USP12 | GRCh38.p7 | 13:27066013 | GTTGTTTTACACACA[C/T]GCAATTCTGTTCTAG | 219333 |
rs9551356 | snp | C/G | 0.483053 | 0.0904792 | intron-variant | USP12 | GRCh38.p7 | 13:27085894 | CTATGCAGCAGGCGT[C/G]GTATCTAGCTCCTGT | 219333 |
rs9553959 | snp | C/T | 0.0887219 | 0.191022 | intron-variant | USP12 | GRCh38.p7 | 13:27084224 | cacacacacaAATTC[C/T]TGTctgggtgtggtg | 219333 |
rs9553960 | snp | G/T | 0.424348 | 0.179172 | intron-variant | USP12 | GRCh38.p7 | 13:27085693 | AACTTCTGTAAAGTT[G/T]TCTTTCCAGAAACTT | 219333 |
rs9553961 | snp | A/T | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27086197 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 219333 |
rs9553964 | snp | A/G | 0.293551 | 0.246177 | intron-variant | USP12 | GRCh38.p7 | 13:27102366 | TGGTCTCCTGCCTCT[A/G]CTCTCATGCTGCCCA | 219333 |
rs9553968 | snp | C/T | 0.492823 | 0.0594727 | intron-variant | USP12 | GRCh38.p7 | 13:27111618 | TAACAAACATCCCAC[C/T]GCAAGTATTTTTTAT | 219333 |
rs9553969 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27112471 | tttttttttttttaa[A/G]agacagggtctcact | 219333 |
rs9553971 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136817 | GGTAAAAATACAATA[G/T]TTAAGTaataaaatg | 219333 |
rs9553973 | snp | C/T | 0.4944 | 0.0526182 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151223 | gtaatcccagctact[C/T]gggagtctgaggcac | 219333 |
rs9553974 | snp | C/T | 0.441295 | 0.160954 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151285 | gccgtgagccaagat[C/T]cagcgacaaagcaag | 219333 |
rs9553975 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155294 | caccatgttggccaa[A/G]atggtcttgatctcc | 219333 |
rs9579069 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27098704 | ATGCCAGGTAAGTAT[C/G/T]TGTGcatgtaccaaa | 219333 |
rs9579070 | snp | C/T | 0.142609 | 0.225759 | intron-variant | USP12 | GRCh38.p7 | 13:27104926 | TACATTAAACAAAAG[C/T]CAGAATTCTACATGT | 219333 |
rs9579071 | snp | A/C | 0.148326 | 0.228391 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27125374 | AGAGATAAGAGAATA[A/C]GTGTCAAAACTATGT | 219333 |
rs9579072 | snp | C/T | 0.312104 | 0.242163 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133455 | AACATGGTGAAACCC[C/T]GTCTCCACTAAAAAA | 219333 |
rs9579073 | snp | C/G | 0 | 0 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27171008 | GCGGCGCGAGGAAAT[C/G]TGCACTTGACTTCCG | 219333 |
rs9581809 | snp | C/T | 0.133093 | 0.220981 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068867 | ATATGCTTCTATACA[C/T]ACTGAACCAGGCAAA | 219333 |
rs9581810 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27076125 | AATCTATTTTTTCTA[C/T]CAATCTATATGATGC | 219333 |
rs9581811 | snp | C/T | 0.106633 | 0.204807 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137067 | TAAGTGACAAAGATA[C/T]TGAACAAAGATAGTG | 219333 |
rs9581813 | snp | A/C | 0.070242 | 0.174573 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142328 | aaagacgaaaaaagg[A/C]gactgagataactga | 219333 |
rs9581814 | snp | A/G | 0.308166 | 0.243139 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144097 | TAGTCCCAGCCTCTC[A/G]GGAGGCTGAGGTGGG | 219333 |
rs9581815 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155504 | TAAATATTACAAATA[C/G]AAATACAAATAAATG | 219333 |
rs9581816 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163778 | TGTCTTAAAAAAAAA[A/G]AAAAAAAGAAAAAAA | 219333 |
rs9581817 | snp | A/G | 0.5 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163786 | AAAAAAAAAAAAAAA[A/G]AAAAAAAAAAAAGAA | 219333 |
rs9581818 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163787 | AAAAAAAAAAAAAAG[A/G]AAAAAAAAAAAGAAA | 219333 |
rs9634343 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124308 | AAAACCAGATTATGG[C/T]TAAAAAATGGTGTCT | 219333 |
rs9652088 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27101973 | CCCTAGGACTGACAA[C/T]CGTGCCTGCCACATA | 219333 |
rs10220079 | snp | G/T | 0 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161607 | GTTAACTACAggcca[G/T]gtgcagtggttcaca | 219333 |
rs10507376 | snp | A/T | 0.114036 | 0.209795 | intron-variant | USP12 | GRCh38.p7 | 13:27069611 | CTTCTAGGTACAGGA[A/T]GAATTATATGAAACC | 219333 |
rs10507377 | snp | A/C | 0.0836354 | 0.186609 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164956 | GAAATTAAATATAAT[A/C]ATATGGCCTCAGTAA | 219333 |
rs10549775 | in-del | -/AAA | | | intron-variant | USP12 | GRCh38.p7 | 13:27116312 | GCAAGACGCTGTCTC[-/AAA]AAAAAAAAAAAAAAA | 219333 |
rs10569845 | in-del | -/AT | 0.309648 | 0.24278 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154072 | CACAGAAATATCCAC[-/AT]CTTTCCACTTTGCCT | 219333 |
rs10578545 | in-del | -/TC | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154331 | CATTTTTGTAACCTC[-/TC]ATGCTACCAAGCCTA | 219333 |
rs11149468 | snp | A/G | 0.274661 | 0.248781 | intron-variant | USP12 | GRCh38.p7 | 13:27074176 | GAGGCCGAGGCGGGC[A/G]GATCACGAGGTCAGG | 219333 |
rs11306580 | in-del | -/A | 0 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152942 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 219333 |
rs11318459 | in-del | -/A | 0.474634 | 0.109726 | intron-variant | USP12 | GRCh38.p7 | 13:27123092 | GTGAGAGTCCATCTC[-/A]AAAAAAAAAAAAAAT | 219333 |
rs11323861 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27088417 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 219333 |
rs11335488 | in-del | -/T | 0.0368353 | 0.130617 | intron-variant | USP12 | GRCh38.p7 | 13:27099689 | TAAAATTCACAATAA[-/T]TTTTTTTCACGTTCA | 219333 |
rs11365356 | in-del | -/A | 0.468047 | 0.122292 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133647 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 219333 |
rs11365650 | in-del | -/A | 0.131723 | 0.220251 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161543 | TAATTTTATACCTTT[-/A]AAAAAAAATGTTACT | 219333 |
rs11366017 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27114770 | AAAAAAAAAAAAAAA[-/A]CAAACTTGAGCAATA | 219333 |
rs11390415 | in-del | -/A | 0.245606 | 0.249961 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156844 | AAAAGAGAGAGAGAG[-/A]AAAAAATGATTTTAT | 219333 |
rs11421764 | in-del | -/T | 0.325091 | 0.238456 | intron-variant | USP12 | GRCh38.p7 | 13:27122245 | GAATCATCAGGGTGG[-/T]TTCCCCCATACTGTT | 219333 |
rs11455614 | in-del | -/TT | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141012 | TCAGTGTGAAGTCAC[-/TT]TTTTTTTTTTTTTTT | 219333 |
rs11458818 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27076030 | CAAGGCTCCGTCTCA[-/A]AAAAAAAAAAAAAAA | 219333 |
rs11839385 | snp | G/T | 0.148661 | 0.22854 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133896 | caaccctttgggagg[G/T]caaggcaataggatc | 219333 |
rs11839835 | snp | C/T | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27075092 | AGAGAATACAGAATT[C/T]CTAAAAGTTCTATAT | 219333 |
rs11840072 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133586 | gtgagccaatatcgc[A/G]ccactgcgctccagc | 219333 |
rs11840852 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135608 | taatcccagctacta[G/T]ggaggctgagacatg | 219333 |
rs11841364 | snp | A/G | 0.0475351 | 0.146656 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117161 | AATGACTAAAAATTC[A/G]TTTATAGGAACTTTC | 219333 |
rs12861201 | snp | A/C | 0 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148708 | atataaataataata[A/C]cagcacaaaagaggt | 219333 |
rs12864575 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126030 | ctctctagattccac[C/T]tctgggggcagggca | 219333 |
rs12865483 | snp | C/T | 0.26326 | 0.249648 | intron-variant | USP12 | GRCh38.p7 | 13:27112163 | taaactgttgtttac[C/T]agtttcttcacctgc | 219333 |
rs12868800 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | USP12 | GRCh38.p7 | 13:27079450 | TCCCTTCTCCAGTAG[C/T]CCAAGGGGGAGTCCT | 219333 |
rs12874243 | snp | C/T | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27119178 | GTCACAGTAATACAT[C/T]TTTTCTGCTCCGTGC | 219333 |
rs12876307 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27107020 | TTTTAAAAAACAAAA[A/C]CAGCAACAACAAAAA | 219333 |
rs17072003 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156134 | CCAGCCTCATCATTA[C/T]AAAGAGACACGACAT | 219333 |
rs17072006 | snp | A/G | 0.0912534 | 0.193131 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156220 | TCAACTCCTGCAAGG[A/G]AAAAAAAAAAAAAAA | 219333 |
rs17072239 | snp | A/G | 0.0869089 | 0.189476 | intron-variant | USP12 | GRCh38.p7 | 13:27112922 | TTTAACCACCATAAT[A/G]TCAATAGCATTACTT | 219333 |
rs17085172 | snp | C/T | 0.040671 | 0.13668 | intron-variant | USP12 | GRCh38.p7 | 13:27074031 | GGATAAAAGACGGGA[C/T]CCAAGGCTGACCCAG | 219333 |
rs17085173 | snp | A/G | 0.040671 | 0.13668 | intron-variant | USP12 | GRCh38.p7 | 13:27074657 | TATTTAATAAGGCCA[A/G]TTATAGGTATGTACG | 219333 |
rs17085180 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | USP12 | GRCh38.p7 | 13:27091391 | CTTCATTTGAAATGT[C/T]CCTTTTATGATCATG | 219333 |
rs17085196 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | USP12 | GRCh38.p7 | 13:27109311 | TGAACAACTGAATAT[C/T]GTGTGTCTTTTAATA | 219333 |
rs17085198 | snp | A/G | 0.030665 | 0.119967 | intron-variant | USP12 | GRCh38.p7 | 13:27110615 | TTCAGAAAAAGAGGC[A/G]CTTAAGCTTAAGAGG | 219333 |
rs17085200 | snp | C/T | 0.0872718 | 0.189788 | intron-variant | USP12 | GRCh38.p7 | 13:27110750 | AATTTACCCAGTATC[C/T]AGTATAAATCTGTCT | 219333 |
rs17085202 | snp | C/T | 0.0872718 | 0.189788 | intron-variant | USP12 | GRCh38.p7 | 13:27111068 | TTCTGTCCAACATGA[C/T]TTGCTCATCTTCTGA | 219333 |
rs17085207 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | USP12 | GRCh38.p7 | 13:27115028 | TTTTATTTCTGAGCA[C/T]AATTCACAATGTTCA | 219333 |
rs17085226 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131188 | GTGGGTACATTACAA[A/G]GAAGAAAGGTAAGAA | 219333 |
rs17085232 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136094 | AAAGTAAACCGCTTT[C/T]CATGTTCTGTTTAAC | 219333 |
rs17085238 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147404 | ATTATCAGCTGAGAC[A/G]TAACAATTCTGGATA | 219333 |
rs17085241 | snp | C/G | 0.0520825 | 0.152737 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153941 | ACTGAGGTATCAAAT[C/G]TAATTATGGCAGTCG | 219333 |
rs17085244 | snp | G/T | 0.0524604 | 0.153226 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157675 | TTTCTCTCTTGTTAT[G/T]TTAATTCACTTCTCA | 219333 |
rs17085247 | snp | C/G | 0.0908922 | 0.192833 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158019 | CTGATTGCGCCATTA[C/G]TTTTACTGGGTGAAC | 219333 |
rs17085251 | snp | A/T | 0.0836354 | 0.186609 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164675 | AAATGGTCAAATGTT[A/T]TATGTAAGTTTTTCA | 219333 |
rs17085261 | snp | A/C | 0.0517044 | 0.152246 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166509 | GACATCATCTCGCTG[A/C]AACTGGCCAACATGG | 219333 |
rs17085263 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166804 | TTTCTGCTAACTATA[C/T]CACTTTACCCTCTAA | 219333 |
rs17085268 | snp | C/T | 0.084364 | 0.187256 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166846 | CATATAACCTGTCAA[C/T]GCCCTAGTACCCTAC | 219333 |
rs17085270 | snp | C/T | 0.114738 | 0.210248 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167007 | GTAAACAGTGTAAAA[C/T]TATATCTAGGGAATA | 219333 |
rs17519439 | snp | A/C | 0.0941369 | 0.195465 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068998 | AATAAAGAGAAAATG[A/C]GTGCCAATGACTGGA | 219333 |
rs17519942 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | USP12 | GRCh38.p7 | 13:27098267 | AAACTATGAACTTCT[A/G]TATGGCAAAGTCAAC | 219333 |
rs17520180 | snp | C/T | 0.141934 | 0.225437 | intron-variant | USP12 | GRCh38.p7 | 13:27105518 | TATCACTGTATAACG[C/T]AATGCAAACATTAAC | 219333 |
rs17520404 | snp | A/C | 0.0543475 | 0.155628 | intron-variant | USP12 | GRCh38.p7 | 13:27111304 | GTCCTAAGACCTAAA[A/C]ATTATCTTTCAAGAG | 219333 |
rs17591685 | snp | A/G | 0.0785177 | 0.181917 | intron-variant | USP12 | GRCh38.p7 | 13:27086775 | TCTTACTTATCCAAC[A/G]GTCTTAGGTACTTTC | 219333 |
rs17591930 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | USP12 | GRCh38.p7 | 13:27098312 | GTGACGAACAAGGAT[A/G]ATTATTTGCATATTA | 219333 |
rs17592082 | snp | C/T | 0.093417 | 0.194889 | intron-variant | USP12 | GRCh38.p7 | 13:27105327 | ATGGGGGAAATGACA[C/T]GCTCTCTATCTAAGG | 219333 |
rs17592221 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | USP12 | GRCh38.p7 | 13:27109326 | TGTGTGTCTTTTAAT[A/G]TATCTTACCTCCTAT | 219333 |
rs17592825 | snp | G/T | 0.307919 | 0.243198 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147232 | CTGCCTTTTTAAAGA[G/T]CTAGCACTGCACAAT | 219333 |
rs17856742 | snp | C/G | | | missense | USP12 | GRCh38.p7 | 13:27095657 | CCTGAAAAATCTCAT[C/G]AACCCACGTTGGGTC | 219333 |
rs28376624 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27077369 | TATTAATAAATGGCA[A/G]TCAGGTAAGATTAGG | 219333 |
rs28412752 | snp | A/T | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27103610 | TATCAAAAAAAAAaa[A/T]aataataataataat | 219333 |
rs28475250 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27086264 | GCACATATACATATA[C/T]ATACACATATATATA | 219333 |
rs34036221 | in-del | -/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27088842 | TGGATGTTGAGCACT[-/G]GTGAGTCCTTCTAGG | 219333 |
rs34049950 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162310 | ACAGATATGCAGCCG[-/A]AAAGTCAGGAATAAA | 219333 |
rs34147620 | in-del | -/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158117 | ATAGGGTCTTTACAG[-/T]AAGTAATCAAGTTAC | 219333 |
rs34160453 | in-del | -/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27170047 | TCCTTTTGAAATTGA[-/C]TAAGATAATAATTGG | 219333 |
rs34237870 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163745 | GTAGGAGACAGCCTG[-/A]AGCAATAGAGCAAGA | 219333 |
rs34292870 | in-del | -/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27099474 | TTACTTCCCAAACCC[-/T]TTCAATTTTTAAAGT | 219333 |
rs34304475 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137354 | TTCAATCCGCTTTAT[-/A]AAAAGACTCAGTTAT | 219333 |
rs34384911 | in-del | -/AA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163768 | AGCAAGACCTGTCTT[-/AA]AAAAAAAAAGAAAAA | 219333 |
rs34396330 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27072115 | ATACTTTTTTTTTTT[A/T]AACTATGGAGGATGA | 219333 |
rs34459313 | in-del | -/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27081724 | TAAATAATAACAATT[-/G]GAAAGTCAAAATAAC | 219333 |
rs34470664 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27119199 | TGCTCCGTGCAAAAG[C/T]TAAGAAATGACAAGA | 219333 |
rs34498931 | in-del | -/A | 0.495559 | 0.0469148 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164090 | ATCCCTACAAAAAGG[-/A]AAAAAAAAAAAATCA | 219333 |
rs34499826 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27108675 | TAAAATGACATTTTA[A/G]GCTGGGTACAATGGC | 219333 |
rs34500454 | snp | A/T | 0.5 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27077908 | CACTGTCATTGTTTT[A/T]AAAAAAAAAGTGGTC | 219333 |
rs34546271 | in-del | -/G | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116999 | ATCGTTACACATGAT[-/G]CGTATTTTCATAATA | 219333 |
rs34583802 | in-del | -/A/TAATAA | | | intron-variant | USP12 | GRCh38.p7 | 13:27103610 | ATCAAAAAAAAAAAT[-/A/TAATAA]TAATAATAATAATAA | 219333 |
rs34653426 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP12 | GRCh38.p7 | 13:27072593 | TGCTTGCCCAAATAC[C/G]CCTTCAGTACAATAG | 219333 |
rs34804303 | in-del | -/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27088455 | GGCGTGCTTGCATGG[-/T]ATGGTCCTTTTTAGC | 219333 |
rs34819649 | in-del | -/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27109476 | GGCCAAGTTTGAAAT[-/G]GGGAATAGTCTCTAG | 219333 |
rs34851889 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27112746 | TTGAAATAACATACA[A/G]CCATATCATATACAG | 219333 |
rs34880978 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146148 | GCTCACTCCTGTAAT[-/A]CCCAGCACTTTGGGA | 219333 |
rs34920378 | in-del | -/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27081827 | TCCATCAGAGCTCTT[-/G]GGGTGATCACATGTA | 219333 |
rs34937145 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27074939 | AAACTAACAGATCTC[-/A]AAAGTTCTAGGAAAT | 219333 |
rs35049812 | in-del | -/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165478 | ATACTTTTTACCACA[-/G]GGGAGGGGAGCAAAT | 219333 |
rs35288040 | in-del | -/CT | 0.493247 | 0.0577133 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154328 | ATCCATTTTTGTAAC[-/CT]CTCATGCTACCAAGC | 219333 |
rs35296226 | in-del | -/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126544 | AGGCATTTAAACGTT[-/C]CCAACCGCAGGCTGG | 219333 |
rs35379046 | in-del | -/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154394 | TTGGTAGCTAATTTT[-/C]CCTGAATGTTCCACT | 219333 |
rs35447833 | in-del | -/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27100890 | ATAATTCCCTACAGC[-/G]GGCTAACTACATATT | 219333 |
rs35532017 | in-del | -/T | 0.482609 | 0.0916147 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165056 | AAAAAGCTGGTGTGC[-/T]TTTTTTTTTTTTTAG | 219333 |
rs35532790 | in-del | -/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27097229 | CAGCACTCTGGGAGG[-/C]CCAAGGCAGGTGGAT | 219333 |
rs35554240 | in-del | -/A | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066976 | CATTAAGAAGAAAAA[-/A]GTAAATGTAAAACTG | 219333 |
rs35561375 | in-del | -/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137776 | AATGACGGAAGAGAT[-/G]GGGATGTCACTTCTG | 219333 |
rs35589231 | in-del | -/A | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124641 | CTTCCCAGAGGTGGG[-/A]AAAAGCACGTGACCT | 219333 |
rs35640193 | in-del | -/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27102792 | TCTGCTTCCCCACGA[-/G]GGGTGTCAGGTACCT | 219333 |
rs35720279 | in-del | -/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161755 | GCATGGTAGTGTGTG[-/C]CCTGTAGTCCCAGAT | 219333 |
rs35733701 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27071339 | CTGGTCATCAATTTT[-/A]AAAATCAAATAATTA | 219333 |
rs35826310 | in-del | -/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152697 | TTGTAATCCCAGCAC[-/T]TTTGGGAGGCCGAGG | 219333 |
rs36082265 | in-del | -/TTA | | | intron-variant | USP12 | GRCh38.p7 | 13:27096138 | ATTAGCTTACCTGAC[-/TTA]TTATTTCACAAATAT | 219333 |
rs36154055 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27107867 | GGAATGGCAATCATT[-/A]AAAAGTCAGGAAACA | 219333 |
rs41300570 | snp | A/T | 0.102696 | 0.201994 | intron-variant | USP12 | GRCh38.p7 | 13:27090002 | ATTTATTTTGTAGAT[A/T]CCAGGAAATCATGTA | 219333 |
rs41491447 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162769 | AGTTCATTAATCATA[A/G]TAATCCAAATGGTTC | 219333 |
rs55686307 | in-del | -/AAATTAAAAA | 0 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161905 | AAAAAAAATAAAAAA[-/AAATTAAAAA]GCCACTCATTAACTG | 219333 |
rs55714288 | snp | A/G | 0.0930568 | 0.194599 | intron-variant | USP12 | GRCh38.p7 | 13:27107542 | CTTATAACTCTGAAA[A/G]TGTATGTCTGTGTGC | 219333 |
rs55737145 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27120450 | CTAAGATCAGGAGTT[A/C]GAGACCAGCCTGGCC | 219333 |
rs55775046 | snp | A/G | 0.0718919 | 0.175435 | intron-variant | USP12 | GRCh38.p7 | 13:27088314 | CCAGCTACTCGGGAG[A/G]CTGAGGCAGGAGAAT | 219333 |
rs55778211 | snp | A/T | 0.0271762 | 0.113356 | intron-variant | USP12 | GRCh38.p7 | 13:27069965 | AAAAAGGCAACTTCT[A/T]GTGGTCCAACCTAAC | 219333 |
rs55780734 | snp | A/G | 0.077417 | 0.180873 | intron-variant | USP12 | GRCh38.p7 | 13:27087312 | GTGCATGCAGGGAGC[A/G]GGGGCAGGAAGGCAG | 219333 |
rs55816785 | in-del | -/TGTGTGTGTGTGTG | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27087270 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGTGTG]CGCGCACGCTCGTGT | 219333 |
rs55832837 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144211 | CTCCCAAAAAAAAAA[-/A]GTGTCAGCCAAGTGT | 219333 |
rs55837621 | in-del | -/A/AA/AAA/T | 0.379354 | 0.213933 | intron-variant | USP12 | GRCh38.p7 | 13:27098366 | ATATACAGAATATTT[-/A/AA/AAA/T]AAAAAAAAACCCTTT | 219333 |
rs55962584 | snp | A/G | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067720 | CAGTTTTAGCAAAAG[A/G]ACTTTAGAAAATGAC | 219333 |
rs55973953 | in-del | -/A | 0.483708 | 0.088773 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143099 | AGAAAAAAAAAAAAA[-/A]GAGTGAAAGAACAAT | 219333 |
rs55974838 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27075961 | CTTGAACCCAGGAGG[A/C/G]GGAGGTTGCAGTGAG | 219333 |
rs56020533 | snp | A/G | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27068957 | TACTGCACCCCCAAG[A/G]AATTCAAAGCATTAT | 219333 |
rs56043082 | snp | A/G | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066212 | ATAGTGCCTTCTTCA[A/G]GAACCT | 219333 |
rs56082282 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | USP12 | GRCh38.p7 | 13:27094377 | GGTGATGGCATGCAC[C/T]GTAGTCCTAGTTACT | 219333 |
rs56139734 | in-del | -/A | 0.188946 | 0.24243 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156220 | TCAACTCCTGCAAGG[-/A]AAAAAAAAAAAAAAA | 219333 |
rs56205760 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27073572 | AGTCAGGCATCTCAG[A/C]TCAGTATATTGTGAG | 219333 |
rs56210732 | snp | C/T | 0.0573587 | 0.15934 | intron-variant | USP12 | GRCh38.p7 | 13:27087695 | TGGCTTGTTCCAGAG[C/T]AGGGGCAAAGAAAGA | 219333 |
rs56246816 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | USP12 | GRCh38.p7 | 13:27089280 | CACACATAGGAAAAC[A/G]TCCCTGTTGCTGGGA | 219333 |
rs56253021 | snp | C/T | 0.0726307 | 0.176182 | intron-variant | USP12 | GRCh38.p7 | 13:27081192 | AGCATGTGATGCTGT[C/T]TGACAGCATTTTATC | 219333 |
rs56256207 | snp | C/G | 0.16911 | 0.236552 | intron-variant | USP12 | GRCh38.p7 | 13:27080162 | CATGCAGGCAGGGAG[C/G]CAGGAGGCATCAACT | 219333 |
rs56261639 | snp | C/T | 0.126564 | 0.217402 | intron-variant | USP12 | GRCh38.p7 | 13:27081997 | GCAGGGTAGATTCAG[C/T]GTAATTCTTAAGAAC | 219333 |
rs56298640 | snp | C/T | 0.125528 | 0.21681 | intron-variant | USP12 | GRCh38.p7 | 13:27088227 | AGATCAAGACCATCC[C/T]AACACAGTGAAACCC | 219333 |
rs56311173 | in-del | -/AA | 0.499598 | 0.0141716 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144500 | GGCAAGACTCTCTTT[-/AA]AAAAAAAAAAAAAAA | 219333 |
rs56365661 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | USP12 | GRCh38.p7 | 13:27100890 | AATAATTCCCTACAG[C/T]GGCTAACTACATATT | 219333 |
rs56673711 | in-del | -/GAA | 0.0926964 | 0.194308 | intron-variant | USP12 | GRCh38.p7 | 13:27102010 | GTATTTCCCATTTTT[-/GAA]TAATGAATGAATGAA | 219333 |
rs56715131 | in-del | -/G | 0.0509478 | 0.151255 | intron-variant | USP12 | GRCh38.p7 | 13:27111914 | ATGGCTATCAAAACT[-/G]AAAAAGATACCTTCC | 219333 |
rs56792204 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | USP12 | GRCh38.p7 | 13:27115999 | CAAGTTAGAAACTAT[C/G]TATCTCCAAGATTTT | 219333 |
rs56820212 | snp | C/G | 0.0520825 | 0.152737 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144120 | GAGGTGGGAGGATCA[C/G]TTCAGCCTGGGAGCT | 219333 |
rs56940748 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | USP12 | GRCh38.p7 | 13:27087963 | TTACAATCTCAAAAT[A/G]CTTCCACATAAAATA | 219333 |
rs56989115 | in-del | -/A | 0.0520825 | 0.152737 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145844 | AAATGGAAGAAAAGC[-/A]AAAAAAATCTTGAGA | 219333 |
rs57105623 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | USP12 | GRCh38.p7 | 13:27121973 | AGATGAGACTCTAAG[A/C]AGACTTTTAAAAAGA | 219333 |
rs57188284 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157495 | ATGAGTTCTGTAAGC[C/T]ACAAATGTGATTTTT | 219333 |
rs57259528 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141376 | ACGTATGATTAAAAA[-/A]CCATGACACCTCTGT | 219333 |
rs57318848 | in-del | -/AATG/G/GAACG | 0.282686 | 0.251287 | intron-variant | USP12 | GRCh38.p7 | 13:27102011 | TATTTCCCATTTTTT[-/AATG/G/GAACG]AATGAATGAATGAAT | 219333 |
rs57387706 | in-del | -/AATG | | | intron-variant | USP12 | GRCh38.p7 | 13:27102040 | ATGAATGAATGAATG[-/AATG]GACAATAGGGATTGA | 219333 |
rs57397733 | in-del | -/A | 0.0584853 | 0.160693 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158156 | ATTAGGGTGGACCCT[-/A]AATCCAGTGTGACTG | 219333 |
rs57508951 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27088439 | AAAAAAAAAAAAAAA[-/A]TGGCGTGCTTGCATG | 219333 |
rs57515458 | snp | C/T | 0.100588 | 0.200439 | intron-variant | USP12 | GRCh38.p7 | 13:27073607 | GCAATTCTAAAAATC[C/T]AGCATGATTTAAGTA | 219333 |
rs57629989 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27106719 | TTTTTTTTAAAAAAA[-/A]TGAGGAAGGATAAAC | 219333 |
rs57634843 | in-del | -/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27103610 | TATCAAAAAAAAAAA[-/T]AATAATAATAATAAT | 219333 |
rs57654990 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27110873 | GAATAGGCAACAGGG[C/G]AATTGAACAACTTCC | 219333 |
rs57840694 | in-del | -/TAAT | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149211 | ATTGATTTACGGAAT[-/TAAT]AAAATAAAAGAGGAA | 219333 |
rs57854009 | in-del | -/A/AA | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27108543 | ATAAAAAAAAAAAAA[-/A/AA]GAAATGTACAATGTG | 219333 |
rs57878571 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27085151 | GTATTATAAATGGAA[C/T]GTTTTCTTTTTTCTT | 219333 |
rs57930303 | in-del | -/A | 0.212425 | 0.24716 | intron-variant | USP12 | GRCh38.p7 | 13:27120622 | AGCAAAACTCCATCT[-/A]AAAAAAAAAAAAAAA | 219333 |
rs58041428 | snp | A/G | 0.0119091 | 0.0762411 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27172820 | TTTTTCCTATTTGAG[A/G]AAGTAGTTCAAGTGA | 219333 |
rs58080631 | snp | A/T | 0.331874 | 0.236213 | intron-variant | USP12 | GRCh38.p7 | 13:27103613 | CAAAAAAAAAAATAA[A/T]AATAATAATAATAAT | 219333 |
rs58131407 | snp | G/T | 0.046775 | 0.145601 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160790 | ATGTTTCTTTTTTTT[G/T]TTTTTCCCCCTTCAA | 219333 |
rs58309351 | in-del | -/GTGTGCCTGCAGTCCCAGCCACTTGC | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141991 | GTGGTACATGATGGC[-/GTGTGCCTGCAGTCCCAGCCACTTGC]AAGGCTGAAGCAGGA | 219333 |
rs58332072 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135050 | AGCACTTTGGGAGGA[C/T]GAGGTGGGCAAATCC | 219333 |
rs58342229 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141330 | GTGAAGTCACTTTTT[A/T]AAACATTTCCTTGCT | 219333 |
rs58373221 | snp | C/T | 0.138886 | 0.22395 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168676 | TTGAAAATGTACTCA[C/T]TGCAATCTAAACATA | 219333 |
rs58500654 | in-del | -/AAAA | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27109926 | CAAAAAAAAAAAAAA[-/AAAA]GTCATCTTTGAGACA | 219333 |
rs58616879 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | USP12 | GRCh38.p7 | 13:27105371 | CCAATGAGTTAACAC[A/G]CATGAAAGCATTATG | 219333 |
rs58703534 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136970 | ATAATACTATTTTGT[C/G]TACTTCAATATACAT | 219333 |
rs58705654 | in-del | -/CTGCAGCTGACAGCAGTCTAG | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117458 | CTGACAGCAGTCTAG[-/CTGCAGCTGACAGCAGTCTAG]ATGGGCCATTGTTAG | 219333 |
rs58765757 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160681 | CATCAGTCTGAAGAA[-/A]TTATCAGCTTTAAAC | 219333 |
rs58819148 | snp | C/G | 0.138886 | 0.22395 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168679 | AAAATGTACTCACTG[C/G]AATCTAAACATAATC | 219333 |
rs58820564 | in-del | -/CACACA/CACACACACACACACA | 0 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148814 | ACACACACACACACA[-/CACACA/CACACACACACACACA]AAAATCAGGTGACAA | 219333 |
rs58958898 | in-del | -/A | 0.466204 | 0.125522 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148127 | CTCAAAAAAAAAAAA[-/A]GACTTTTCTAAAACG | 219333 |
rs59164229 | in-del | -/TATA/TATATA | 0 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148692 | ATATATATATATATA[-/TATA/TATATA]ATATAAATAATAATA | 219333 |
rs59231507 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141926 | TGGTAGCTCATGCCT[A/G]TAATCATGCACTTTG | 219333 |
rs59419270 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | USP12 | GRCh38.p7 | 13:27122370 | TCACCTCCTCCCATG[A/G]TTCTGAGCCCTCCCC | 219333 |
rs59460436 | in-del | -/GCA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129246 | GGAAAGAACAAAGCA[-/GCA]TCTCTGCCAGTCCTG | 219333 |
rs59527642 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128443 | AACAATACAAAAAAC[C/T]TTCAAAAAATTAATA | 219333 |
rs59784746 | in-del | -/TG | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27079215 | CGTGCTCCCTGTGTG[-/TG]GGGCGGGGGGGAGTG | 219333 |
rs59894509 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | USP12 | GRCh38.p7 | 13:27097853 | AGCAGTGGTTGGGAC[C/T]TCAGACTGCTTCAGA | 219333 |
rs59926086 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152569 | GATAAATGCAAAACT[C/T]TAAAAGCCACTAAAT | 219333 |
rs60033236 | in-del | -/A/AAA/G | 0.179105 | 0.239737 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163777 | TGTCTTAAAAAAAAA[-/A/AAA/G]AAAAAAAAGAAAAAA | 219333 |
rs60064156 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27170016 | ATTGTCACTGTAAAA[A/G]ACCTAATTATCGCAT | 219333 |
rs60175468 | in-del | -/TG | 0.5 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27087123 | GTGTGTGTGTGTGTG[-/TG]CGTGTGTGAGAGTGT | 219333 |
rs60193498 | in-del | -/T | 0.999173 | 0.00480552 | intron-variant | USP12 | GRCh38.p7 | 13:27106845 | TTACTTTGTACCCCC[-/T]ATCTTTTCTAAAATA | 219333 |
rs60197468 | in-del | -/TT | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067137 | GGCATGTTTTTTTTT[-/TT]AATGCAAAAATGTAA | 219333 |
rs60200963 | snp | C/G | 0.0349115 | 0.127424 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152419 | CCAAAGTCCAAAGCA[C/G]ATAATTATATAAACA | 219333 |
rs60289123 | snp | A/G | 0.126219 | 0.217206 | intron-variant | USP12 | GRCh38.p7 | 13:27083201 | CATAGCAACATCAAC[A/G]ATAACTGATCATGTA | 219333 |
rs60297541 | in-del | -/AAAG | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141689 | TAAATGAATAGACAG[-/AAAG]GAAGTATTTTTCTTG | 219333 |
rs60302094 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | USP12 | GRCh38.p7 | 13:27090877 | TTGTTCATCGAACAA[C/T]TCAGTAAGTTGTCAT | 219333 |
rs60364289 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150670 | CGAGACTGCAATGAG[C/T]TATAACTGCAGTCAT | 219333 |
rs60395417 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167218 | GGTGAGCCAAGATTG[A/C]AGCATTGCACTCCAG | 219333 |
rs60432004 | in-del | -/AA | 0.366266 | 0.221319 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129164 | TCTTACCACAATAAG[-/AA]AGTGACCTGTAGCTC | 219333 |
rs60533914 | in-del | -/GTGTGT | | | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117616 | ACATAAAACACCAAC[-/GTGTGT]GTGTGTGTGTGTTTA | 219333 |
rs60579167 | in-del | -/CTTA | | | intron-variant | USP12 | GRCh38.p7 | 13:27107527 | AAATATCAACATAAA[-/CTTA]TAACTCTGAAAATGT | 219333 |
rs60672263 | snp | G/T | 0.0244538 | 0.107838 | intron-variant | USP12 | GRCh38.p7 | 13:27120318 | TTTTATGAAATCAGT[G/T]ATTCTTTACTGGGAT | 219333 |
rs60862615 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | USP12 | GRCh38.p7 | 13:27119983 | CTCTCTCTAGCCTAA[C/T]GCTAACTAAAAAGGC | 219333 |
rs61032561 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | USP12 | GRCh38.p7 | 13:27087494 | AGATAAAGAGATCAA[C/T]AGACGTAGAAGAGAA | 219333 |
rs61084865 | in-del | -/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27112468 | CATTTTTTTTTTTTT[-/T]AAGAGACAGGGTCTC | 219333 |
rs61109673 | in-del | -/AA | | | intron-variant | USP12 | GRCh38.p7 | 13:27114785 | AAAAAAAAAAAAAAA[-/AA]CAAACTTGAGCAATA | 219333 |
rs61393785 | snp | G/T | 0.0532157 | 0.154195 | intron-variant | USP12 | GRCh38.p7 | 13:27082787 | AGAGAGGTAGGAGGG[G/T]GAAAACGTCAGGTGG | 219333 |
rs61450995 | in-del | -/AAC | 0.126219 | 0.217206 | intron-variant | USP12 | GRCh38.p7 | 13:27083476 | AGCCAGGGACAGGAA[-/AAC]AACAACTGAAACAGC | 219333 |
rs61499075 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151871 | TTCCACAGAAGATAC[A/G]CAAATGGCCAATAAG | 219333 |
rs61614819 | in-del | -/A | 0.248471 | 0.249995 | intron-variant | USP12 | GRCh38.p7 | 13:27093309 | ACCCGAAAAAAAAAA[-/A]CCCACTTAAAATTCG | 219333 |
rs61661368 | in-del | -/TGTGTGTGTG | | | intron-variant | USP12 | GRCh38.p7 | 13:27087274 | GTGTGTGTGTGTGTG[-/TGTGTGTGTG]CGCGCACGCTCGTGT | 219333 |
rs61690916 | snp | A/C | 0.0520825 | 0.152737 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146226 | AGCCAACATGGTGAA[A/C]CCCTGTGTCTACTAA | 219333 |
rs61944155 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154828 | ATCACAAGGGTCTGG[A/T]AAGTGAAAGAGGGAA | 219333 |
rs61944156 | snp | A/G | 0.5 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156444 | GTGACGAAACGCAAC[A/G]ATGATCATTATGGAT | 219333 |
rs61946482 | snp | G/T | 0.0726307 | 0.176182 | intron-variant | USP12 | GRCh38.p7 | 13:27072566 | TGTGGAGATTAAAGA[G/T]ATACCAACAACTGCT | 219333 |
rs61946485 | snp | C/T | 0.078151 | 0.181571 | intron-variant | USP12 | GRCh38.p7 | 13:27081506 | TCCTCCACTGAAGTT[C/T]GAATCCCTCAAAGTC | 219333 |
rs61946488 | snp | A/T | 0.0777841 | 0.181223 | intron-variant | USP12 | GRCh38.p7 | 13:27085756 | TATGTGGGGAATATG[A/T]GTATATACACACAAA | 219333 |
rs61946490 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | USP12 | GRCh38.p7 | 13:27089616 | TCATCAGGAAAGCCT[C/T]AAAGCCAAATATTTT | 219333 |
rs61946499 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133533 | CCGGTGGGGCTGAGG[C/T]AGGAGAATGGCATGA | 219333 |
rs61946500 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144198 | AGTAAGACTCTGACT[A/C]CCAAAAAAAAAAAGT | 219333 |
rs66799174 | snp | A/T | 0.297521 | 0.245442 | intron-variant | USP12 | GRCh38.p7 | 13:27110128 | TTTCCTTTTCCAGGT[A/T]AAAAAAAAAAAAAAA | 219333 |
rs66849824 | snp | A/G | 0.0952156 | 0.196321 | intron-variant | USP12 | GRCh38.p7 | 13:27075696 | ATTTTTCAAACACAC[A/G]TCTCTTATAATAAGG | 219333 |
rs66994402 | in-del | -/A | 0.486464 | 0.0811471 | intron-variant | USP12 | GRCh38.p7 | 13:27116312 | GCAAGACGCTGTCTC[-/A]AAAAAAAAAAAAAAA | 219333 |
rs67071903 | snp | C/T | 0.0952156 | 0.196321 | intron-variant | USP12 | GRCh38.p7 | 13:27075632 | ACACAGCACTCAATA[C/T]GGCTCCAAAACAGAT | 219333 |
rs67171711 | snp | C/T | 0.100588 | 0.200439 | intron-variant | USP12 | GRCh38.p7 | 13:27069984 | GTCCAACCTAACATA[C/T]ATCCAAGAAAAATGA | 219333 |
rs67186044 | snp | A/G | 0.494315 | 0.0530107 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163115 | AAGCAAATTTTGAAA[A/G]ATCAATGTAATTCAA | 219333 |
rs67271626 | in-del | -/AGC | 0.365024 | 0.221967 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129242 | AAGTGGAAAGAACAA[-/AGC]AGCATCTCTGCCAGT | 219333 |
rs67331574 | snp | C/G | 0.103082 | 0.202275 | intron-variant | USP12 | GRCh38.p7 | 13:27072180 | GCTTTAAGTCTATTT[C/G]TGTATTTATTTAGGC | 219333 |
rs67692913 | snp | A/G | 0.115438 | 0.210697 | intron-variant | USP12 | GRCh38.p7 | 13:27073506 | TAAGGCTGGGGAAAG[A/G]GTTGGGTTAATTTTA | 219333 |
rs67819325 | in-del | -/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163778 | GTCTTAAAAAAAAAA[-/G]AAAAAAAGAAAAAAA | 219333 |
rs68153510 | snp | C/G | 0.126564 | 0.217402 | intron-variant | USP12 | GRCh38.p7 | 13:27086151 | CTCCAGCCTGGGTGA[C/G]AGAGAGAGATCTTTT | 219333 |
rs71083624 | in-del | -/A | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27081031 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 219333 |
rs71083627 | in-del | -/TGTGTG | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27086304 | TAGGAGGTGCTGCAT[-/TGTGTG]TGTGTGTGTGTGTGT | 219333 |
rs71083629 | in-del | -/TT | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27094199 | CCACTTTATGATGAC[-/TT]TTTTTTTTTTTTTTT | 219333 |
rs71083630 | in-del | -/A | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27097985 | AAAAAAAAAAAAAAA[-/A]GTACTATATAAAGTT | 219333 |
rs71083631 | in-del | -/TTCG | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27102017 | TCATTCATTCATTCA[-/TTCG]TTCATTAAAAAATGG | 219333 |
rs71083632 | in-del | -/TT | 0 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144519 | AGTTGACCTACCACC[-/TT]TTTTTTTTTTTTTTT | 219333 |
rs71083634 | in-del | -/AAA | 0 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155097 | GCGAGGTTCCGTCTC[-/AAA]AAAAAAAAAAAAAAA | 219333 |
rs71188772 | in-del | -/G | 0.5 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27098037 | GTTGCCCAGGATGGA[-/G]TGCAACTTCATATAG | 219333 |
rs71425184 | snp | A/T | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27086193 | AAAAAAAAAAAAAAA[A/T]AAAAATATATATATA | 219333 |
rs71425185 | snp | A/T | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27086195 | AAAAAAAAAAAAAAA[A/T]AAATATATATATATA | 219333 |
rs71431293 | multinucleotide-polymorphism | AA/TT | 0 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163106 | AAAAAAATACAAGCA[AA/TT]TTTTTTAAGATCAAT | 219333 |
rs71431294 | multinucleotide-polymorphism | GA/TT | 0 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163111 | ATACAAGCATTTTTT[GA/TT]AAGATCAATGTAATT | 219333 |
rs71847627 | in-del | -/AATT | 0.0418186 | 0.138422 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149208 | AAGATTGATTTACGG[-/AATT]AATAAAATAAAAGAG | 219333 |
rs72053574 | in-del | -/A | | | intron-variant | USP12 | GRCh38.p7 | 13:27108537 | TAAAGCATAAAAAAA[-/A]AAAAAAGAAATGTAC | 219333 |
rs72206222 | in-del | -/TG | | | intron-variant | USP12 | GRCh38.p7 | 13:27087100 | CAGAGGGGAAGGGGC[-/TG]TGTGTGTGTGTGTGT | 219333 |
rs72246154 | in-del | -/TA | 0.454904 | 0.143228 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148377 | GCAACTGTATAAAAC[-/TA]TATATATATATTATA | 219333 |
rs72464119 | in-del | -/ACACAC | | | intron-variant | USP12 | GRCh38.p7 | 13:27086283 | CACATATATATAATT[-/ACACAC]ACACACACACACACA | 219333 |
rs72513593 | in-del | -/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154331 | CATTTTTGTAACCTC[-/T]CATGCTACCAAGCCT | 219333 |
rs73155859 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27066566 | AACATTTCCCTCTTT[C/G]CCTGTTCCCAAGCCT | 219333 |
rs73155860 | snp | A/C | 0.029116 | 0.117091 | intron-variant | USP12 | GRCh38.p7 | 13:27071279 | GCTTCTTTTTTATAC[A/C]CCTTACCTATTCTTG | 219333 |
rs73155861 | snp | A/G | 0.100588 | 0.200439 | intron-variant | USP12 | GRCh38.p7 | 13:27072332 | GGTGGGGTAAGGACT[A/G]GTAAATTGAAAAAAG | 219333 |
rs73155862 | snp | C/T | 0.103082 | 0.202275 | intron-variant | USP12 | GRCh38.p7 | 13:27072884 | CCCTCCACACTTTCA[C/T]ATGAAGCAAATCTAC | 219333 |
rs73155864 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27074420 | GAAAAAAAAAAAATT[C/G]TAATCAGAGAGCTGG | 219333 |
rs73155868 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | USP12 | GRCh38.p7 | 13:27090958 | AGGTACTGTGCATAG[C/T]GTATTTTATAGACAG | 219333 |
rs73155869 | snp | G/T | 0.0547245 | 0.156101 | intron-variant | USP12 | GRCh38.p7 | 13:27094725 | TCTGATTTTAAAAAG[G/T]TGAGGGAGGCATATT | 219333 |
rs73155870 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | USP12 | GRCh38.p7 | 13:27096306 | GGGTAAGCCCAGAAC[A/G]TGGGGCTTTTCAAAG | 219333 |
rs73155871 | snp | A/G | 0.0693013 | 0.172766 | intron-variant | USP12 | GRCh38.p7 | 13:27096801 | AATTACCTATTTAGG[A/G]CATTTTATTTTTAGA | 219333 |
rs73155872 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27097192 | AAAAAGCAGGCCAAG[C/T]GCAGTGGCTCATGCC | 219333 |
rs73155874 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | USP12 | GRCh38.p7 | 13:27097732 | GAAGATTAAAAGTGC[C/T]TAGAATACAACAATA | 219333 |
rs73155875 | snp | A/C | 0.0547245 | 0.156101 | intron-variant | USP12 | GRCh38.p7 | 13:27097887 | GAGAATATTTTCATA[A/C]ACATAATGAGATATT | 219333 |
rs73155876 | snp | A/T | 0.17461 | 0.238362 | intron-variant | USP12 | GRCh38.p7 | 13:27099454 | TGCATATTCTTCATA[A/T]ACAATTACTTCCCAA | 219333 |
rs73155877 | snp | A/C | 0.0547245 | 0.156101 | intron-variant | USP12 | GRCh38.p7 | 13:27100558 | CTCTCTCCACTTTGC[A/C]TCCTGCACCAACCTT | 219333 |
rs73155878 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | USP12 | GRCh38.p7 | 13:27100615 | TGACGTGCATGCACC[C/T]CAATCCCGTACAATT | 219333 |
rs73155879 | snp | C/T | 0.0700422 | 0.173537 | intron-variant | USP12 | GRCh38.p7 | 13:27100662 | TCACTCACCCACCCA[C/T]TTCCGGGTCACAAAT | 219333 |
rs73155881 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | USP12 | GRCh38.p7 | 13:27102464 | TCTCGTGGTTTCCCA[C/T]GGCTTTCCAAATAAA | 219333 |
rs73155882 | snp | C/T | 0.0700422 | 0.173537 | intron-variant | USP12 | GRCh38.p7 | 13:27102980 | CTGTGCAACAGTCCT[C/T]TTATGCTATGATTAG | 219333 |
rs73155885 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | USP12 | GRCh38.p7 | 13:27106389 | TCTCCACTCTAGTAA[C/T]TGGGGCGAGACGGGG | 219333 |
rs73155886 | snp | C/T | 0.17138 | 0.237316 | intron-variant | USP12 | GRCh38.p7 | 13:27108785 | AACATGGTGAAACCC[C/T]GTCTCTAACTGAAAT | 219333 |
rs73155889 | snp | C/G | 0.0543475 | 0.155628 | intron-variant | USP12 | GRCh38.p7 | 13:27109618 | TGATTTACAAACCAA[C/G]TATAAAAAGTCATCT | 219333 |
rs73155891 | snp | A/T | 0.0486741 | 0.148216 | intron-variant | USP12 | GRCh38.p7 | 13:27112289 | CATTTCATAGCTACT[A/T]TTTTTTTTTTTTTCC | 219333 |
rs73155892 | snp | A/G | 0.0869089 | 0.189476 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27118000 | ACCTTGAAAATTCCC[A/G]GGAAAACATACTAGA | 219333 |
rs73155893 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | USP12 | GRCh38.p7 | 13:27119433 | CTGTAGATCATCATC[A/G]TTTAACCCTTCTGGA | 219333 |
rs73159772 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130361 | CAGAGATAGTAAGAC[A/G]GAAACTTCAGTGACC | 219333 |
rs73159774 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137674 | TTAAAGTGTTCCCCC[A/G]ATCTCAGCCTGCTAG | 219333 |
rs73159775 | snp | A/C | 0.0648419 | 0.167978 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142138 | AAAACACACACACAG[A/C]CACACACACACGCAA | 219333 |
rs73159777 | snp | C/T | 0.0640965 | 0.167152 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143200 | CATCAAAAAGAATGA[C/T]TGTAATTGATTATTA | 219333 |
rs73159778 | snp | A/C | 0.0637235 | 0.166737 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144928 | AAAAATCAGCCAGGC[A/C]TGGCGGCATATGCCT | 219333 |
rs73159780 | snp | C/G | 0.0513262 | 0.151752 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147366 | TCTATGAGAATGCTT[C/G]TAATATTTAAGTATA | 219333 |
rs73159781 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149625 | AGAGGCTGCAGATGT[A/G]GGGGGTGGGAGGAGT | 219333 |
rs73159784 | snp | A/C | 0.0322114 | 0.122752 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152126 | ACCACAATTCCACTC[A/C]AAAGTACAGACACAT | 219333 |
rs73159785 | snp | A/G | 0.104859 | 0.203554 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153409 | TATATACATATGCAT[A/G]CAAAAACATATAAAG | 219333 |
rs73159787 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155974 | TTAAAAATATTTCTT[A/T]AAAAAAACCTATAGA | 219333 |
rs73159789 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156240 | AAAAAAAAAAATCAA[A/G]GAATCTGGTTCAGGC | 219333 |
rs73159790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158360 | AACCAACCCTGTCGA[C/T]ATCCTGATTCTGGAC | 219333 |
rs73159791 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160919 | TAAGCCCAGCATCCA[C/T]CAGCTCTTCTTCCTG | 219333 |
rs73159793 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164798 | TAAAGTATGGTGTAG[A/G]TATGTAAATATCCCT | 219333 |
rs73159797 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27172586 | GGCGATAAATTTATA[A/G]TAGGCTTCTAAATAT | 219333 |
rs73159798 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173368 | ATAAATAGCTGTGGT[C/T]ATCCTGTCCTTCCCA | 219333 |
rs73497349 | snp | A/G | 0.222333 | 0.248464 | intron-variant | USP12 | GRCh38.p7 | 13:27079363 | ACCACAAGGTAGCTG[A/G]GGTTTTATATGCTCT | 219333 |
rs73497360 | snp | C/G | 0.0520825 | 0.152737 | intron-variant | USP12 | GRCh38.p7 | 13:27087133 | TGTGTGCGTGTGTGA[C/G]AGTGTGTGTGTGTTT | 219333 |
rs73497361 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | USP12 | GRCh38.p7 | 13:27089476 | GATACCAAACCAGTC[C/T]TACAATAACATGCTA | 219333 |
rs73497364 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | USP12 | GRCh38.p7 | 13:27091460 | TGCATGAGTTACTAC[A/G]TTTATATTTGCGATT | 219333 |
rs73497365 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP12 | GRCh38.p7 | 13:27092163 | AAATCTAACAAAACA[C/T]GCATGGTATTGATAT | 219333 |
rs73497368 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP12 | GRCh38.p7 | 13:27093661 | TACAATCCAGTGATC[C/T]TGCTCCTTGATATTT | 219333 |
rs73497373 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | USP12 | GRCh38.p7 | 13:27100382 | CATTCTGTTCTAAAC[A/G]AACTCCCTCGCCTTA | 219333 |
rs73497375 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | USP12 | GRCh38.p7 | 13:27102217 | ACAGTCCAGTTGAGG[A/G]TCAACTCTAGCTAAC | 219333 |
rs73497395 | snp | A/G | 0.0125001 | 0.0780626 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117803 | CACAGTTTCAAGAAC[A/G]TGATCAACTCAATTC | 219333 |
rs73497397 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | USP12 | GRCh38.p7 | 13:27119407 | GGCCAAGAGGAGTAA[A/G]GTGGAAAGAGCTGTA | 219333 |
rs73499314 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137420 | AAAAATCAATTGTCA[A/G]TATTATAGAAATGGA | 219333 |
rs73499323 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142530 | CACTTAAGTTTTTAC[A/G]AATGTACACACAAAT | 219333 |
rs74041144 | snp | C/T | 0.137527 | 0.223271 | intron-variant | USP12 | GRCh38.p7 | 13:27087282 | GTGTGTGTGTGTGTG[C/T]GCGCGCACGCTCGTG | 219333 |
rs74041145 | snp | G/T | 0.0360663 | 0.129354 | intron-variant | USP12 | GRCh38.p7 | 13:27088829 | GCTGTGAGCACGCTT[G/T]GATGTTGAGCACTGT | 219333 |
rs74041147 | snp | A/T | 0.030665 | 0.119967 | intron-variant | USP12 | GRCh38.p7 | 13:27094635 | CACAACATGAATGAT[A/T]TATTATTATTAGCCA | 219333 |
rs74041148 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | USP12 | GRCh38.p7 | 13:27095343 | CCACAACATGGTTCT[A/G]TGGCCTCCTAAACTG | 219333 |
rs74041149 | snp | G/T | 0.012005 | 0.0765399 | intron-variant | USP12 | GRCh38.p7 | 13:27095563 | CTTTAACATAGTAAT[G/T]CAATTTTTCTCTATA | 219333 |
rs74041173 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | USP12 | GRCh38.p7 | 13:27098780 | AATATCCTAAATGTT[C/T]ATCAACAGGAGAATG | 219333 |
rs74041178 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | USP12 | GRCh38.p7 | 13:27099558 | AGTCACCTCCCTTCA[C/T]TTAACCCACTAAGTC | 219333 |
rs74041179 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | USP12 | GRCh38.p7 | 13:27100339 | TCTTTGTTCCCAACC[C/G]TTTCTAAGTTGCTCA | 219333 |
rs74041186 | snp | G/T | 0.0279636 | 0.114961 | intron-variant | USP12 | GRCh38.p7 | 13:27102373 | CTGCCTCTACTCTCA[G/T]GCTGCCCAGGCCCAC | 219333 |
rs74041187 | snp | A/G | 0.127599 | 0.217986 | intron-variant | USP12 | GRCh38.p7 | 13:27102837 | GTATCATCAGTTCCT[A/G]AACAGTGTCTGGCAC | 219333 |
rs74041190 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | USP12 | GRCh38.p7 | 13:27102988 | CAGTCCTCTTATGCT[A/G]TGATTAGGTAACATG | 219333 |
rs74041192 | snp | G/T | 0.0410537 | 0.137264 | intron-variant | USP12 | GRCh38.p7 | 13:27109570 | ACACAACAATCAAAT[G/T]GCAAATGTAAATGCT | 219333 |
rs74041195 | snp | A/T | 0.5 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27114769 | CCTCCTCTCCATTTT[A/T]AAAAAAAAAAAAAAA | 219333 |
rs74041196 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | USP12 | GRCh38.p7 | 13:27115612 | AAACTACCACAACAA[C/T]TATATAGCACAAGTT | 219333 |
rs74041197 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | USP12 | GRCh38.p7 | 13:27115656 | AGTGACTCAGAACAG[A/G]TAACATTCAGGTAAA | 219333 |
rs74041198 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | USP12 | GRCh38.p7 | 13:27115658 | TGACTCAGAACAGGT[A/T]ACATTCAGGTAAAAC | 219333 |
rs74041199 | snp | A/G | 0.0372196 | 0.131242 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116960 | ACGAAATGGCCTAAC[A/G]ATACATTTCTCACAC | 219333 |
rs74041201 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | USP12 | GRCh38.p7 | 13:27118886 | ACCCCACATGTCCAC[C/T]TGTCACCATATGTAC | 219333 |
rs74041202 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | USP12 | GRCh38.p7 | 13:27119258 | TATAATACAAAAAAA[C/T]AGATACTCTCCTTAG | 219333 |
rs74042503 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156093 | GCTGCCAGCAGCTCC[A/G]TAACAGAAGAGTCAT | 219333 |
rs74042504 | snp | C/T | 0.139225 | 0.224118 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168471 | GCAAAACACAGCCTC[C/T]CTACATGTATTCTGT | 219333 |
rs74042505 | snp | C/T | 0.175254 | 0.238565 | intron-variant, downstream-variant-500B | USP12, USP12-AS1 | GRCh38.p7 | 13:27169301 | TGCTTAAGAGACAGG[C/T]ACACACACTCGCCAG | 219333 |
rs74042506 | snp | A/G | 0.175254 | 0.238565 | intron-variant, downstream-variant-500B | USP12, USP12-AS1 | GRCh38.p7 | 13:27169335 | AGAAGGATACGGGGT[A/G]TGGCAGGGAGGAGCG | 219333 |
rs74042507 | snp | A/C | 0.175254 | 0.238565 | intron-variant, downstream-variant-500B | USP12, USP12-AS1 | GRCh38.p7 | 13:27169366 | TTCCAAGCCTAGCAA[A/C]ACAGCACCTACAAAG | 219333 |
rs74042525 | snp | A/G | 0.0718919 | 0.175435 | intron-variant, downstream-variant-500B | USP12, USP12-AS1 | GRCh38.p7 | 13:27169469 | ACTGCAAATTACTTT[A/G]AGATATTCAGCACTA | 219333 |
rs74262398 | in-del | -/TTT | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165067 | GTGCTTTTTTTTTTT[-/TTT]AGTATAAAATAAGGT | 219333 |
rs74360206 | snp | G/T | 0.494315 | 0.0530107 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163111 | ATACAAGCAAATTTT[G/T]AAAAATCAATGTAAT | 219333 |
rs74388505 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | USP12 | GRCh38.p7 | 13:27081478 | TGCTGTTTCCACCAC[A/C]TCTACAGTGACTTCC | 219333 |
rs74460613 | snp | C/T | 0.5 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27079005 | TGATAAAAAAAAAAA[C/T]TAGAAAATCCCCCCA | 219333 |
rs74484406 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27093320 | ACCCGAAAAAAAAAA[A/C]CCACTTAAAATTCGA | 219333 |
rs74493249 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | USP12 | GRCh38.p7 | 13:27098889 | ATGGCAAAACTTCCA[A/C]AACAGAAAGTGAAAC | 219333 |
rs74514498 | snp | A/T | 0.5 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137409 | TAGTAAACAAAAAAA[A/T]TCAATTGTCAATATT | 219333 |
rs74525816 | snp | A/C | 0.5 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166383 | AGAGCTAGAATAAAT[A/C]TGAGTTTAAAGGCAG | 219333 |
rs74579884 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159099 | TAAACTCACACAATT[G/T]TGCAGTTTTAAAAAT | 219333 |
rs74591228 | snp | C/T | 0.126219 | 0.217206 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160795 | TCTTTTTTTTTTTTT[C/T]CCCCCTTCAACCTTA | 219333 |
rs74669997 | snp | A/G | 0 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152957 | AAAAAAAAAAAAAAA[A/G]AAGAAAGAAAGAAAA | 219333 |
rs74683580 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168855 | AGATTTGCCCAGGTA[C/T]GTTATTTTGACAAAT | 219333 |
rs74727160 | snp | C/T | 0.0908922 | 0.192833 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146089 | TCTTTTATAATCAAT[C/T]AAACAGTAAAATTTC | 219333 |
rs74818270 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129246 | GGAAAGAACAAAGCA[G/T]CATCTCTGCCAGTCC | 219333 |
rs74881590 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156330 | AAGGGGATGCAATCA[C/G]CAAAGTACAGAAAAT | 219333 |
rs74972967 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | USP12 | GRCh38.p7 | 13:27079803 | GAACTTACCAACATC[C/T]TGTCAGCAGAGAAGT | 219333 |
rs75104322 | snp | C/G | 0.0170251 | 0.090679 | intron-variant, downstream-variant-500B | USP12, USP12-AS1 | GRCh38.p7 | 13:27169297 | TCCCTGCTTAAGAGA[C/G]AGGCACACACACTCG | 219333 |
rs75134831 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP12 | GRCh38.p7 | 13:27106223 | AAACGTTACATGAAA[A/C]AGTCACCAGTATGAC | 219333 |
rs75196045 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127289 | TGGCAGAAGCTTGCA[A/G]AAGGCTTAAAATCAG | 219333 |
rs75256486 | snp | C/G | 0.0919752 | 0.193722 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154278 | TACATATACTCTGTT[C/G]AGCAAGGGCATATAG | 219333 |
rs75390341 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | USP12 | GRCh38.p7 | 13:27106901 | CAAAAATAAACAAAA[A/C]CTAAATGTATATGGA | 219333 |
rs75453028 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | USP12 | GRCh38.p7 | 13:27073511 | CTGGGGAAAGAGTTG[A/G]GTTAATTTTAAAAGG | 219333 |
rs75479714 | snp | A/C | 0.5 | 0 | downstream-variant-500B | USP12 | GRCh38.p7 | 13:27065893 | ACCCTCTAAGATTCT[A/C]TGACTCTCAATGTTC | 219333 |
rs75483691 | snp | C/T | 0.5 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144764 | TTTTTTTTTTTCCCC[C/T]AGAAATCGGGAGGAG | 219333 |
rs75489155 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | USP12 | GRCh38.p7 | 13:27121480 | AAGAGATTTGAGTTC[A/T]TAAGTCAAAAATTAC | 219333 |
rs75528984 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP12 | GRCh38.p7 | 13:27109361 | TATTCTTGCCTTAAG[C/T]AAAATCACTAAACTT | 219333 |
rs75534289 | snp | A/T | 0.0520825 | 0.152737 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148358 | CTCTTAATTGATTTA[A/T]AAAGCAACTGTATAA | 219333 |
rs75549424 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | USP12 | GRCh38.p7 | 13:27101758 | ATTTATGCTCTTTTG[A/G]AGAAAAAGAATTGTT | 219333 |
rs75569368 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | USP12 | GRCh38.p7 | 13:27113334 | TGTTGAAAAGGAACC[A/G]TTTTTGAAGAAGCAC | 219333 |
rs75597260 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | USP12 | GRCh38.p7 | 13:27084851 | GTTCTTTTCTCTCAA[G/T]ATTATTCAACTATTT | 219333 |
rs75608716 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145162 | CCTTTCCTTCCAAAT[C/T]GCAGGTCTCCTCAAC | 219333 |
rs75611362 | snp | A/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148388 | AAACTATATATATAT[A/T]TTATAGGCCAGGCAT | 219333 |
rs75678597 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156914 | GTAACAGCATGATCC[A/G]GCGGCAAAAGCACTA | 219333 |
rs75680351 | snp | A/G | 0.5 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27094754 | TTCTCAAAAAAAAAA[A/G]GACCATGTAAATGTT | 219333 |
rs75687686 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27110125 | GGATTTCCTTTTCCA[A/G]GTAAAAAAAAAAAAA | 219333 |
rs75694903 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067961 | CAGAATGAAGTCTTA[A/G]CAAACACAGATTTTA | 219333 |
rs75743282 | snp | A/G | 0.5 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27097180 | TTAAAAAAAAAAAAA[A/G]AGCAGGCCAAGCGCA | 219333 |
rs75752081 | snp | A/T | 0.021333 | 0.101051 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27154450 | ACTGGTAGTGTGCTA[A/T]CAGTACCTGAAGTAA | 219333 |
rs75774951 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | USP12 | GRCh38.p7 | 13:27082280 | TGTACTTTTATCTCA[C/T]GGAGACAGCTTCTTT | 219333 |
rs75817761 | snp | C/T | 0.0966517 | 0.197444 | intron-variant | USP12 | GRCh38.p7 | 13:27092165 | ATCTAACAAAACACG[C/T]ATGGTATTGATATGA | 219333 |
rs75886081 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | USP12 | GRCh38.p7 | 13:27074059 | CAGGCAATGGAGGAA[A/G]AAGACGATTATTAAA | 219333 |
rs75960433 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126756 | ACTACTGTAGAGTTA[C/G]CAAAGTTTAAATTTA | 219333 |
rs75999413 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067048 | ACGGTGTAGATGTGA[A/G]CAAGTATGTGATTAC | 219333 |
rs76027794 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170971 | TTTCCCCCAGCGCGG[A/G]GTCGGGGACTCGGCC | 219333 |
rs76084318 | snp | A/G | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27097179 | TTTAAAAAAAAAAAA[A/G]AAGCAGGCCAAGCGC | 219333 |
rs76087864 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165224 | GTTCCCAGATAAAAG[A/G]AATAAATTATTCTAT | 219333 |
rs76088040 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132693 | TGTGAGGAGCTGGTG[A/G]GCACGTTAACAAGAA | 219333 |
rs76140027 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148298 | TACCTGTAACAGCAA[C/T]TGTTAATTATAAAGG | 219333 |
rs76152169 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166740 | AAGTCTTATCTTTGT[G/T]ATAACTAAGTGCCTA | 219333 |
rs76167913 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27134167 | GTTTAATTAGTCACA[C/T]ATTATGACTGAAATG | 219333 |
rs76204568 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27111990 | TTACTTTTTAAATCA[A/C/T]GGTATCCAATTTGTA | 219333 |
rs76209713 | snp | A/G | 0.104859 | 0.203554 | intron-variant, nc-transcript-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168953 | TGCTGATTCTGAGAA[A/G]TGTTCTGTTTAAGTC | 219333 |
rs76211776 | snp | A/T | 0.494315 | 0.0530107 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163112 | TACAAGCAAATTTTG[A/T]AAAATCAATGTAATT | 219333 |
rs76213633 | snp | C/T | 0.0901694 | 0.192235 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158588 | CACAAACCTGTACAG[C/T]ATATGACTGTACTGG | 219333 |
rs76216625 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151538 | TGTAATCCCAGTGCT[C/T]TCGGAGGACTAGGCA | 219333 |
rs76353533 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130674 | AAGGTATTATTAAAT[A/C]AATCGTATCAACGGT | 219333 |
rs76360122 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27092595 | CATCTTTGACAAAGG[A/C]GCAAAGGCAATTCAA | 219333 |
rs76370636 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27119305 | CAATTCCATGAAGCG[A/G]CCCCCAGAGGTATCA | 219333 |
rs76376334 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170715 | ACAAATACCATCGCC[A/T]TGGCAGGCGGTCCCC | 219333 |
rs76400875 | snp | C/T | 0.0966517 | 0.197444 | intron-variant | USP12 | GRCh38.p7 | 13:27080295 | TCCCTATTGCTGATA[C/T]GATTTTGACATGATA | 219333 |
rs76407407 | snp | A/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27110127 | ATTTCCTTTTCCAGG[A/T]AAAAAAAAAAAAAAA | 219333 |
rs76444779 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | USP12 | GRCh38.p7 | 13:27079271 | AGGATTCAATCTCAA[A/G]CAAAATCCCAGGAAG | 219333 |
rs76535486 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164439 | AGAAGCTAATGGTCC[C/T]TCTGAAAGAGAAGCA | 219333 |
rs76606509 | snp | A/C | 0.5 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27094744 | GGGAGGCATATTCTC[A/C]AAAAAAAAAAGACCA | 219333 |
rs76626173 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | USP12 | GRCh38.p7 | 13:27073196 | GAGAGTGAGACAGGA[A/G]AAAGAGTAAGACCCT | 219333 |
rs76652701 | snp | A/G | 0.245916 | 0.249967 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155441 | TAAACTTGTGGTAAT[A/G]TGTTACAGCCCCATT | 219333 |
rs76764539 | snp | A/C | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27076031 | CAAGGCTCCGTCTCA[A/C]AAAAAAAAAAAAAAA | 219333 |
rs76826004 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | USP12 | GRCh38.p7 | 13:27096224 | GCCAACTGCTTTAGA[A/C]CCACAAAGTTTATCA | 219333 |
rs76881888 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138418 | AGAAGCAATGTCTTG[C/G]GCAGCTGAGAGATGG | 219333 |
rs76902711 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136634 | TTAAATTAGAGAAGA[C/T]AGACTTTTCTGACTT | 219333 |
rs76912112 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153018 | CTTTTTTGATTAATT[G/T]TTTACATTCAACATT | 219333 |
rs77088886 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147920 | ATCACTGGAGCCCAG[G/T]AGTTCAAGACCAACT | 219333 |
rs77152778 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | USP12 | GRCh38.p7 | 13:27081596 | CCTCCCATGAATCAC[A/C]AATATTCTAATGGCA | 219333 |
rs77323897 | snp | C/G | 0.5 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27087455 | GCTACAAGATTATCA[C/G]TGTGTATTCACGGTT | 219333 |
rs77378545 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159644 | TTATCTAAACTCAAA[C/G]TTTCCTACACCTTTA | 219333 |
rs77405427 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | USP12 | GRCh38.p7 | 13:27099467 | TAAACAATTACTTCC[C/T]AAACCCTTTCAATTT | 219333 |
rs77430729 | snp | A/C/T | 0.0111237 | 0.0737856 | intron-variant | USP12 | GRCh38.p7 | 13:27120257 | CAATAATAATAGCTC[A/C/T]ATTCCCACATTTGAG | 219333 |
rs77527164 | snp | A/G | 0.106987 | 0.205054 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124863 | AAACACCATGTGCCC[A/G]GAAACTGAATCAAAG | 219333 |
rs77599757 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27085164 | AATGTTTTCTTTTTT[C/T]TTTCTTTCTTTCTTT | 219333 |
rs77675536 | snp | A/G | 0.0905309 | 0.192535 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158467 | AGAAATTGACTGTTA[A/G]GCAATTTCATCATGG | 219333 |
rs77720269 | snp | A/T | 0.0715223 | 0.175059 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157535 | TACATGCCTTTTTTT[A/T]AAAAAAATATAAGTT | 219333 |
rs77815401 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149794 | GGATGGTTTCAGGAT[C/G]AAACTGTTCTCAGAT | 219333 |
rs77912463 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153383 | TTCAATTTTGTTTTT[C/T]AGATAAAACATATAT | 219333 |
rs77958281 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145930 | TAATGATCCAGATTT[C/T]GTTTTAAAAATCATG | 219333 |
rs77964990 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127341 | ACCCTCAGTAAGATA[C/T]ATGGTACCAATGACA | 219333 |
rs77993388 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | USP12 | GRCh38.p7 | 13:27085096 | TATACAAGTCTTCTG[C/T]CATGTAAGTTTATTC | 219333 |
rs78001967 | snp | C/T | 0.5 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156614 | CCTGAGGTCAGAAGT[C/T]TGAGACCAGCCTGGC | 219333 |
rs78011900 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27170790 | GGCTGAAGTAAACAA[A/G]TGACAGGAAAGCTAA | 219333 |
rs78046507 | snp | C/G | 0.5 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27079978 | GAGAAAGACACTAAG[C/G]TGACTCAGTGAGATA | 219333 |
rs78048308 | snp | A/C | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27109917 | ACTCTGTCTCCAAAA[A/C]AAAAAAAAAGTCATC | 219333 |
rs78065088 | snp | A/C | 0.105214 | 0.203807 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168320 | TCCTACAACCCAAAC[A/C]GGAAGAGACAATAAT | 219333 |
rs78083978 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27110126 | GATTTCCTTTTCCAG[A/G]TAAAAAAAAAAAAAA | 219333 |
rs78127451 | snp | C/G | 0.5 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137631 | CACTGATAAGCTATT[C/G]TGAATGCAGTGCTGT | 219333 |
rs78188610 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | USP12 | GRCh38.p7 | 13:27101348 | TATATTTAATTTTTA[A/G]AACCCTGGTTTTCTT | 219333 |
rs78189857 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131000 | AAGTAAGGAAGGAAT[A/G]GTGTTGTGCAGCTAT | 219333 |
rs78212926 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165426 | TCCATTTTGGTTAGT[A/G]TATGTTGAGCTAACA | 219333 |
rs78230648 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116695 | ATGATGGTCCTATCA[C/G]ATTACGATGGAGCTG | 219333 |
rs78235577 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | USP12 | GRCh38.p7 | 13:27100312 | TTATTTCCTTTCTCA[C/T]CCTTGGGATTTTCTT | 219333 |
rs78269667 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | USP12 | GRCh38.p7 | 13:27091864 | GACATTACCAATTGC[A/G]TTTCTAAAATACAAG | 219333 |
rs78296085 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155502 | TTTAAATATTACAAA[C/T]AGAAATACAAATAAA | 219333 |
rs78305209 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148815 | ACACACACACACACA[A/C]AAATCAGGTGACAAA | 219333 |
rs78351888 | snp | A/G | 0.5 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152958 | AAAAAAAAAAAAAAA[A/G]AGAAAGAAAGAAAAG | 219333 |
rs78361609 | snp | A/G | 0.0788843 | 0.182262 | intron-variant | USP12 | GRCh38.p7 | 13:27107608 | CTGTCCACTGAAAAG[A/G]TGTGGCAGCAACAAG | 219333 |
rs78394407 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | USP12 | GRCh38.p7 | 13:27078992 | AGAGTATGTCCTCTG[A/G]TAAAAAAAAAAACTA | 219333 |
rs78404722 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159754 | TCCTATATAAGTTCC[C/T]TGGGAAAGCTAAAAT | 219333 |
rs78451070 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | USP12 | GRCh38.p7 | 13:27070145 | AAGAACTACTATTAC[C/G/T]GCAGGCAACAAGAAT | 219333 |
rs78463376 | snp | A/G | 0.5 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156221 | CAACTCCTGCAAGGA[A/G]AAAAAAAAAAAAAAT | 219333 |
rs78470365 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27096554 | CATAGAACAGTAAGG[A/C]CTTTAGAGGCAGTAT | 219333 |
rs78587448 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132698 | GGAGCTGGTGGGCAC[A/G]TTAACAAGAAGAGCA | 219333 |
rs78630701 | snp | C/T | 0.0912534 | 0.193131 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128037 | ATTCAGTATTTTCAA[C/T]GAAAAGTTTCACCAC | 219333 |
rs78665658 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | USP12 | GRCh38.p7 | 13:27115372 | TTATAGGTTTTATGC[A/G]TAGTGCACAGAGACA | 219333 |
rs78720660 | snp | C/G | 0.375 | 0.216506 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167664 | AGAAGTACTATTTTA[C/G]TAATAAAATATTAAT | 219333 |
rs78805222 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | USP12 | GRCh38.p7 | 13:27103936 | ACTAAGATAACATCA[C/T]TGTATAAAGAGCCCA | 219333 |
rs78864885 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | USP12 | GRCh38.p7 | 13:27090916 | TGACTATACAAAGTA[C/T]GTATTTATGCAAATA | 219333 |
rs78893599 | snp | A/C | 0.0707826 | 0.174302 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27172786 | ACCCTGTTCTTCATG[A/C]CTGGCAGCTCAGCTT | 219333 |
rs78915785 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27119306 | AATTCCATGAAGCGG[A/C]CCCCAGAGGTATCAT | 219333 |
rs79021018 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | USP12 | GRCh38.p7 | 13:27073974 | CACTCCTTTAAGATG[A/T]GATCACTCTTAATTT | 219333 |
rs79041388 | snp | G/T | 0.0520825 | 0.152737 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151703 | GGGAGGATGACTTGA[G/T]ACCAGGAGTTGCAAG | 219333 |
rs79119259 | snp | A/T | 0.5 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27099689 | TAAAATTCACAATAA[A/T]TTTTTTTCACGTTCA | 219333 |
rs79162710 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164408 | TCTCTTCTTTAGACA[C/T]AACATACTGTTTAGA | 219333 |
rs79179960 | snp | A/G | 0.0952156 | 0.196321 | intron-variant | USP12 | GRCh38.p7 | 13:27073527 | GTTAATTTTAAAAGG[A/G]GAGAGTGGGGAGGGG | 219333 |
rs79227338 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | USP12 | GRCh38.p7 | 13:27081470 | TGTTCTCTTGCTGTT[G/T]CCACCACATCTACAG | 219333 |
rs79330334 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140394 | TATGAAAACACACAG[C/T]CAAAACTTTTAGAAT | 219333 |
rs79367545 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165009 | AAGTCCTGAAGCTAA[C/T]TTGAATGCACACACC | 219333 |
rs79445983 | snp | G/T | 0.5 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27084497 | GAGAGACAGTGAGAT[G/T]AAAAAAAAAAAAAAA | 219333 |
rs79494509 | snp | C/T | 0 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160800 | TTTTTTTTTTTCCCC[C/T]TTCAACCTTAAGTTA | 219333 |
rs79609876 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160899 | CTCAACCCATCTCCC[C/T]GGGTTAAGCCCAGCA | 219333 |
rs79610170 | snp | C/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27111988 | CTTTACTTTTTAAAT[C/G]ATGGTATCCAATTTG | 219333 |
rs79649735 | snp | A/G | 0.0905309 | 0.192535 | intron-variant | USP12 | GRCh38.p7 | 13:27098762 | TAACAGCAGAAGTCT[A/G]AAAATATCCTAAATG | 219333 |
rs79673607 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159520 | AGCCTTCTCTATCAA[C/T]ATCCAGTAACATTTG | 219333 |
rs79719442 | snp | A/T | 0.5 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27070166 | CAACAAGAATGCATC[A/T]CACAAATATATCAAT | 219333 |
rs79825328 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | USP12 | GRCh38.p7 | 13:27078652 | AGATAAGGAGTCTTA[A/C]CAGAAATAAAGAATA | 219333 |
rs79951482 | snp | G/T | 0.0271762 | 0.113356 | intron-variant | USP12 | GRCh38.p7 | 13:27081463 | TAATTCTTGTTCTCT[G/T]GCTGTTTCCACCACA | 219333 |
rs79976375 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168380 | CTAACAGTAAGTAGT[A/G]CCAGCTCCAAAGCAG | 219333 |
rs79993737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141446 | ATACCATTCTCCACT[A/G]AAAGAAATCAAGACA | 219333 |
rs80045229 | snp | G/T | 0.0633504 | 0.166319 | intron-variant | USP12 | GRCh38.p7 | 13:27083644 | ATTTACAGAGTTCAA[G/T]AGGCATGCTATATAA | 219333 |
rs80157015 | snp | G/T | 0.0763149 | 0.179815 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27125189 | ATGTATGTATGTATT[G/T]GGTTTCATATTATTT | 219333 |
rs80162477 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | USP12 | GRCh38.p7 | 13:27092526 | AACAGATATACGGAC[C/G]AACAGGACAGAAGAC | 219333 |
rs80175881 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP12 | GRCh38.p7 | 13:27119570 | AACTAAGATTTTCAT[A/G]GCTAAAACTATTCAG | 219333 |
rs80206688 | snp | A/C | 0.5 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152943 | CGAGACTCCGTCTCA[A/C]AAAAAAAAAAAAAAA | 219333 |
rs80255461 | in-del | -/T | 0.308908 | 0.242961 | intron-variant | USP12 | GRCh38.p7 | 13:27094967 | GCCTGAGCAACACAG[-/T]TAAGACCCCTGTCTC | 219333 |
rs111271145 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | USP12 | GRCh38.p7 | 13:27092986 | TGGATCACTTGAGGT[C/T]GGGAGTTCAAGACCA | 219333 |
rs111308223 | snp | G/T | 0.5 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136039 | CAGACCCCAATTTTC[G/T]GTCACACTGCTGAGA | 219333 |
rs111314855 | snp | C/T | 0.5 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140144 | CAAAATAGTTTTTTT[C/T]CCCTACGTGTTTTGA | 219333 |
rs111363248 | snp | A/C | 0.5 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147778 | AAAAAAAAAATTTTA[A/C]AAAACCGTCAACCAA | 219333 |
rs111422121 | in-del | -/T | 0.0941369 | 0.195465 | intron-variant | USP12 | GRCh38.p7 | 13:27082152 | CAGTCCTAAACACCC[-/T]CTTTTTCCAATAGAA | 219333 |
rs111424385 | snp | A/C | | | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067981 | CACAGATTTTAATTT[A/C]TGAACACCCTTCCAG | 219333 |
rs111451830 | in-del | -/A/AA/AAA | 0.340108 | 0.233197 | intron-variant | USP12 | GRCh38.p7 | 13:27094183 | ATTGCAAGGGGATTT[-/A/AA/AAA]AAAAAAAAAAAAAAA | 219333 |
rs111456971 | in-del | -/C | 0.153665 | 0.230694 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140144 | AAAATAGTTTTTTTT[-/C]CCCTACGTGTTTTGA | 219333 |
rs111590870 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155116 | AGACGGAACCTCGCT[C/G]TGTCACCCAGACTGG | 219333 |
rs111638218 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139572 | AGTGAGCCGAGATCG[C/T]GCCACTGCACTCCAG | 219333 |
rs111644794 | snp | A/T | 0.5 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27102669 | TACCTAATCAGGGAC[A/T]TTTCCCAATGACTGA | 219333 |
rs111646000 | snp | A/G | 0.5 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27076541 | TAACAATTTTAGGTG[A/G]TTATGGTTCTTTTCT | 219333 |
rs111652465 | snp | C/T | 0 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142149 | ACAGACACACACACA[C/T]GCAATGACAGTGAAG | 219333 |
rs111702298 | in-del | -/A | 0.24449 | 0.249939 | intron-variant | USP12 | GRCh38.p7 | 13:27108530 | TAAAACTTAAAGCAT[-/A]AAAAAAAAAAAAAGA | 219333 |
rs111740264 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163777 | CTGTCTTAAAAAAAA[A/G]AAAAAAAAGAAAAAA | 219333 |
rs111761575 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | USP12 | GRCh38.p7 | 13:27121538 | TGAATAAGAGCCCCA[C/T]GAAGAAATGCAGACA | 219333 |
rs111774611 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP12 | GRCh38.p7 | 13:27100105 | CCATCCCTCCGAGGC[C/T]GGGCCAAGTCATGCA | 219333 |
rs111792658 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067945 | TTCTTAAAACCCCCA[A/G]CAGAATGAAGTCTTA | 219333 |
rs111845654 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139553 | CCTGGGAGGCGGAGG[C/T]TGCAGTGAGCCGAGA | 219333 |
rs111877681 | snp | A/C | 0.5 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130556 | AAAAAAATCACAAAA[A/C]ATGCCAAAAAAAAAA | 219333 |
rs111887736 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141976 | AAAAATTAGTTGGGC[A/G]TGGTACATGATGGCG | 219333 |
rs111891834 | snp | A/G | 5.32231e-05 | 0.00515836 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117840 | CCTGTGGTCCCCGAC[A/G]ACCATGTGAAAGGGA | 219333 |
rs111894278 | snp | A/G | 0.5 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27070640 | CTCACCACAACCTCC[A/G]CCTCCCGGGTTCAAG | 219333 |
rs111926273 | snp | A/G | 0.5 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157742 | CCAAGTTACCTTTCA[A/G]ATTCCACCAAGCTTC | 219333 |
rs112073097 | in-del | -/T | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27072104 | CACCAACAAAAATAC[-/T]TTTTTTTTTTTAACT | 219333 |
rs112160958 | snp | C/T | 0.5 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145145 | TCTTCACTGAACCTC[C/T]TCCTTTCCTTCCAAA | 219333 |
rs112208912 | snp | C/G/T | 3.29538e-05 | 0.00405904 | synonymous-codon, utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27069331 | AGACTCAGAGTTCTT[C/G/T]GAGATATCTGATGTC | 219333 |
rs112258814 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27120451 | TAAGATCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 219333 |
rs112277002 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151272 | GGAGGTGGAGGTTGC[C/T]GTGAGCCAAGATTCA | 219333 |
rs112294741 | snp | C/T | 0.5 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139564 | GAGGCTGCAGTGAGC[C/T]GAGATCGCGCCACTG | 219333 |
rs112401950 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124878 | AGAAACTGAATCAAA[C/G]GCAATGAGAATATTT | 219333 |
rs112412247 | snp | A/G | 0.5 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27079290 | AATCCCAGGAAGAGT[A/G]GCTTCAGCTCAGTGT | 219333 |
rs112452559 | snp | C/T | 0.5 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27109814 | CTCGGGAGGCTGAGA[C/T]AGGAGAATCGCTGGA | 219333 |
rs112471193 | in-del | -/AC | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116791 | TGTTCAGATGCACAC[-/AC]TTATTCCTGTGTTAC | 219333 |
rs112544541 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152738 | ACGAGGTCAGGAGAT[A/G]GAGACCATCCTGGTT | 219333 |
rs112548761 | in-del | -/ATAT | 0.5 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27083858 | AACCTTTTTGGGAGA[-/ATAT]ATATATATATATATT | 219333 |
rs112637263 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173346 | GCCCATCTGTGTGCC[C/T]GTCCTGATAAATAGC | 219333 |
rs112666424 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27135069 | GTGGGCAAATCCCTT[A/G]AGCCCAGAAGTTTGA | 219333 |
rs112724860 | snp | C/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153265 | TGAGCCAAGATCGTG[C/G]CACTGCACTCCAGCC | 219333 |
rs112761419 | in-del | -/GGG | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27172536 | AGAAAGATAAGTAAT[-/GGG]GGAAGGAGAGGAGCG | 219333 |
rs112777742 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141909 | CTGAAAGAGGCTGGG[C/T]GTGGTAGCTCATGCC | 219333 |
rs112790410 | snp | C/T | 0.119978 | 0.213528 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173608 | AGCACTTTGGGAGGC[C/T]GAGGCAGGTGGATCA | 219333 |
rs112870706 | in-del | -/C | 0.5 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27115048 | CACAATGTTCACCAA[-/C]CTTTAATAGTTGGAG | 219333 |
rs112896609 | snp | C/T | 0.5 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27159703 | TGAAATGCCTAGCAA[C/T]AGCATCACCAAGTAG | 219333 |
rs112928560 | snp | A/C | 0.5 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163183 | TATCCTCATGACTGT[A/C]CTCTGGACTTACATT | 219333 |
rs112992687 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138679 | ACTTCAAGATGGTGT[C/T]ACTCTTGCCATGTGA | 219333 |
rs113017983 | snp | C/T | 0.5 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160851 | TGCAGGTTTGTGACA[C/T]AGGTAAACGTATCAT | 219333 |
rs113092443 | snp | A/G | 0 | 0 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27134635 | CCTAAAAAAACCTCA[A/G]ATAAACAATTATGAG | 219333 |
rs113156610 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | USP12 | GRCh38.p7 | 13:27082579 | CTTGGCTGTTTGGTG[C/T]AAGAGGCCTAGCTTT | 219333 |
rs113204576 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132772 | ACCAAAGTGCTATGT[A/G]TGAGCTCTTCTCTGC | 219333 |
rs113240422 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP12 | GRCh38.p7 | 13:27123172 | GTAGAGAGACCATGG[C/T]ATACTACAAGTATCA | 219333 |
rs113323128 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116921 | GGTTTATGTAAGAAC[A/G]CTCTGATGTTCGCAT | 219333 |
rs113418259 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | USP12 | GRCh38.p7 | 13:27074206 | GAGATTAAGACCATC[C/G]TGGCTAACATGGTGA | 219333 |
rs113419409 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP12 | GRCh38.p7 | 13:27074970 | CAGATATAGTACTTG[C/T]AGAGTAATAAATAAT | 219333 |
rs113423353 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149861 | AGATCCCTCGCATGC[A/G]CGGTTCATAACAGGG | 219333 |
rs113488847 | in-del | -/A | 0.0524604 | 0.153226 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131969 | CACAGGCCACCTCCT[-/A]ATTTTTATTACGTGT | 219333 |
rs113517330 | snp | A/C | | | intron-variant | USP12 | GRCh38.p7 | 13:27069777 | ACGTGGAGAAACCCC[A/C]TCTCTATTAAAAATA | 219333 |
rs113531643 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP12 | GRCh38.p7 | 13:27074190 | CAGATCACGAGGTCA[A/G]GAGATTAAGACCATC | 219333 |
rs113611659 | snp | C/G | 0.5 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27085879 | TACAAAAAAAATATA[C/G]TATGCAGCAGGCGTG | 219333 |
rs113631432 | snp | C/T | 0.5 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27070914 | TGCTGGGCTTGGACG[C/T]TGCAGAGTAAGAAGT | 219333 |
rs113711633 | in-del | -/AGACAGTGTGGT | 0.0325976 | 0.123435 | intron-variant | USP12 | GRCh38.p7 | 13:27092488 | AAGCTACGGTAATCA[-/AGACAGTGTGGT]AGTGGGGAAAGAACA | 219333 |
rs113719848 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152120 | GATTAAACCACAATT[C/G]CACTCCAAAGTACAG | 219333 |
rs113735276 | snp | C/T | 0.5 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27106229 | TACATGAAAAAGTCA[C/T]CAGTATGACAGTCTA | 219333 |
rs113766508 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167824 | AACAACGCATGGGCT[C/G]TGAGGTTTGCCCCAG | 219333 |
rs113779599 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128399 | ACATACTTGAGTGCA[C/T]GATGAAACTTTACAG | 219333 |
rs113798072 | snp | A/G | 0.5 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27070815 | GCCTCAGCCTCCCCA[A/G]GTGCTGGGATTACAG | 219333 |
rs113812964 | snp | C/T | 0 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27101907 | CCACGGCACATGAAA[C/T]GCTGCTTGTCCATGC | 219333 |
rs113891840 | snp | A/C | 0.5 | 0 | intron-variant | USP12 | GRCh38.p7 | 13:27076105 | TTTGGACTTGGGTAG[A/C]CTGAAATCTATTTTT | 219333 |
rs113907986 | in-del | -/TGTGTGTGTGTGTG | 0.0912534 | 0.193131 | intron-variant | USP12 | GRCh38.p7 | 13:27087252 | TATAGTGGGGAGGGA[-/TGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 219333 |
rs113938757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150607 | AAATTCATATGGAGG[C/T]CGGACCCAGTGGCTC | 219333 |
rs114002009 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | USP12 | GRCh38.p7 | 13:27122251 | ATCAGGGTGGTTCCC[C/T]CATACTGTTCTCGTG | 219333 |
rs114080221 | snp | C/T | 0.030278 | 0.119257 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155370 | ACAGGTGTGAGCCAC[C/T]GCACCCAGCGACCTC | 219333 |
rs114173145 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | USP12 | GRCh38.p7 | 13:27091152 | AGAGGGAACACAGAC[A/T]ACTCAGAGAGAAAAA | 219333 |
rs114212174 | snp | A/C | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138153 | CTGTTATATAACATG[A/C]GTTCACTTCAGCTGC | 219333 |
rs114214259 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132067 | ATTCTCATATAGCAC[A/G]TAAGAAATCCGGGCT | 219333 |
rs114341473 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27134284 | AGCATAAAAGAAAGC[A/G]TTTTGATCAAAAGCA | 219333 |
rs114351156 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27156434 | AAGAGATATAGTGAC[A/G]AAACGCAACGATGAT | 219333 |
rs114351528 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27118517 | AAATTGATGGGAATA[C/T]TGCAAGCCCTACTAC | 219333 |
rs114404217 | snp | A/T | 0.00795532 | 0.062565 | intron-variant, downstream-variant-500B | USP12, USP12-AS1 | GRCh38.p7 | 13:27169327 | GCCAGACAAGAAGGA[A/T]ACGGGGTGTGGCAGG | 219333 |
rs114408009 | snp | G/T | 0.0162398 | 0.0886349 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067472 | AGGGTAAGGCTTTAG[G/T]AACTATCTTAAAAAG | 219333 |
rs114428264 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167338 | CCTTTTGCTTTCTTG[A/G]AGTTTTTATATTTTC | 219333 |
rs114531534 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | USP12 | GRCh38.p7 | 13:27073582 | CTCAGCTCAGTATAT[G/T]GTGAGTAGAGCAATT | 219333 |
rs114534659 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | USP12 | GRCh38.p7 | 13:27097709 | CCTGTACCTCACAAG[A/G]CTGGGAGGAAGATTA | 219333 |
rs114549041 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | USP12 | GRCh38.p7 | 13:27077748 | TGAAACTCATTATGT[A/G]GATTTTGCAGCAGAA | 219333 |
rs114550934 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146694 | TTCCTACCTTGTTTC[A/G]GAAGGCACTTAAGAT | 219333 |
rs114693016 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP12 | GRCh38.p7 | 13:27111652 | CCTACTACTAAGACC[A/G]TTTTGAGCGCACATC | 219333 |
rs114702958 | snp | C/G | 0.0168055 | 0.0901129 | intron-variant | USP12 | GRCh38.p7 | 13:27091837 | TATAGACACCAGCTT[C/G]CTACCACCTGAGACA | 219333 |
rs114774810 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144410 | TGAGGCAGGATGTTC[A/G]CTTGAGCCCAGGAGG | 219333 |
rs114781827 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116725 | GCCCTACACAGGTGC[A/G]TCTTTATCCTTTACA | 219333 |
rs114857077 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142310 | AAAAATGTCCAAGTC[A/G]ATAAAGACGAAAAAA | 219333 |
rs114957933 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | USP12 | GRCh38.p7 | 13:27103824 | ATTTGGAAAAAATAA[C/T]GAACACTGTAAAAAT | 219333 |
rs114976750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128158 | ATGGAAATATAAGAT[C/T]ACTGGATGCCAAAAA | 219333 |
rs115038697 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | USP12 | GRCh38.p7 | 13:27111070 | CTGTCCAACATGACT[C/T]GCTCATCTTCTGAAT | 219333 |
rs115042109 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP12 | GRCh38.p7 | 13:27080558 | GGGGTCAGGCACACA[C/T]GGAATAAAGGGAGAG | 219333 |
rs115044086 | snp | C/G | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27117302 | TCTGATAGCACACAT[C/G]TCTCAGAGCTGAAGT | 219333 |
rs115105349 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144877 | CCAGCCCGGGTAATA[A/G]GGCCAAATCCTGTCT | 219333 |
rs115139110 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147687 | AACTCCAGTTGAGAC[A/G]AAAGGCTGACTTCTA | 219333 |
rs115143137 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | USP12 | GRCh38.p7 | 13:27100064 | TGAGACAGCCTGCAA[C/T]TCAAAAATCTTCTCA | 219333 |
rs115492738 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | USP12 | GRCh38.p7 | 13:27100172 | AGACCACAGCTAAGC[C/T]AACTGAAGCAAATTA | 219333 |
rs115498585 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | USP12 | GRCh38.p7 | 13:27102425 | CAAACAAATCAGAAC[A/G]TATCACCCACCTGCT | 219333 |
rs115502199 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131372 | ATACAGGAAAATACC[C/T]ACTCTGCCTACCTCG | 219333 |
rs115533597 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165839 | GTGAAATTCTTGCTT[A/T]ATTATGTCTGATTCT | 219333 |
rs115539668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27082309 | TTCCTTAAAACCTCA[C/T]GAACCCACCCCTGCT | 219333 |
rs115586328 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | USP12 | GRCh38.p7 | 13:27098301 | AATGAAGACAAGTGA[C/T]GAACAAGGATAATTA | 219333 |
rs115603624 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153568 | ATTAATCGGTACATT[A/C]GAGTTACAGATCCTT | 219333 |
rs115634855 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144787 | GGGAGGAGCTGGACA[C/T]AGTGGTTCCTGCCTG | 219333 |
rs115647589 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP12 | GRCh38.p7 | 13:27090344 | AACCCCTACCAGATG[C/T]ATAAATAAAACACCA | 219333 |
rs115761953 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142793 | AAAAATCTATCGTGA[A/C]ACAAAAAAGAAGTGG | 219333 |
rs115794025 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27150608 | AATTCATATGGAGGT[C/T]GGACCCAGTGGCTCA | 219333 |
rs115808788 | snp | A/T | 0.0596104 | 0.162024 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067745 | AATGACAATTTTTTT[A/T]AAATTTACTGCCTGA | 219333 |
rs115817668 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | USP12 | GRCh38.p7 | 13:27092137 | ACCCCCCAAAATGAA[C/T]ACTTAAATATAAATC | 219333 |
rs115822679 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27118498 | CAACTTCACAATCCA[C/T]TAAAAATTGATGGGA | 219333 |
rs115888599 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155614 | AGAATTTGAAGTTGC[C/T]TTTGTAAAAGCACAG | 219333 |
rs115893650 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP12 | GRCh38.p7 | 13:27113452 | CACCAACCAGTTCTT[A/G]TTTAGGTGACATTTT | 219333 |
rs115897827 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | USP12 | GRCh38.p7 | 13:27080039 | ACCTGAACTCCAGCA[C/T]GTGTTAAAATGGGGG | 219333 |
rs115899528 | snp | C/T | 0.0410537 | 0.137264 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067421 | GTTGGTAGATCAGGC[C/T]GGCTTATATATAATT | 219333 |
rs115899767 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | USP12 | GRCh38.p7 | 13:27101443 | AGTTAAACAATTTCA[C/T]TCATTCATTCACTCA | 219333 |
rs115901735 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP12 | GRCh38.p7 | 13:27123297 | TCCTCAGATGTAAAA[C/G]TTCTGTCTATAGTAC | 219333 |
rs115958023 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151640 | GTAAAAAATTAGCCA[A/G]GCATAGAGGCATGCA | 219333 |
rs115958412 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161624 | TGCAGTGGTTCACAC[A/G]TGTAATTGCAGCATT | 219333 |
rs116041875 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153875 | CAAAATGAGAAAAAC[A/G]AAGTCTCTAGAAGTC | 219333 |
rs116147074 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132571 | CCCTGGTTGGCTGTA[C/T]GGCTTTGTGAATGAA | 219333 |
rs116162228 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158739 | TGGCAGCCCTAGGAA[A/G]CTAATAAAATTATTG | 219333 |
rs116164717 | snp | C/T | 0.103082 | 0.202275 | intron-variant | USP12 | GRCh38.p7 | 13:27110772 | AATCTGTCTTTAAAA[C/T]TGTATTTGTACTACA | 219333 |
rs116202385 | snp | G/T | 0.0532157 | 0.154195 | intron-variant | USP12 | GRCh38.p7 | 13:27107735 | AGAAATGTACAATGT[G/T]CCTTCTCAAAAGAAG | 219333 |
rs116252834 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | USP12 | GRCh38.p7 | 13:27113502 | TCCCCCTACCCACCA[C/T]GCTTCTTACTCCAGC | 219333 |
rs116279394 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | USP12 | GRCh38.p7 | 13:27093538 | AAATGTCAGCAAGGA[C/T]GTGGAGAAACAAGAA | 219333 |
rs116288082 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP12 | GRCh38.p7 | 13:27106819 | TCTGAAAGAATGTTG[C/T]TATAAAACATTTACT | 219333 |
rs116326384 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136223 | AATAAAGACCCTTGG[C/T]GGGGCGCGGTGCTCA | 219333 |
rs116342767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27082372 | CTCTCTCAGCCTTCA[C/T]AGAACTGAAGACAGG | 219333 |
rs116442199 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132256 | AACTAGAAAGAGTAG[A/T]TACTTGAAGGGTAGC | 219333 |
rs116478935 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP12 | GRCh38.p7 | 13:27106082 | GACTGCATTATATTA[C/T]ACATTTTAAAATACA | 219333 |
rs116533058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27080972 | GACTGCTGACTGATC[A/G]GGATGGTGGTTGCTG | 219333 |
rs116655506 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | USP12 | GRCh38.p7 | 13:27120292 | ACGACCCTATCAAAA[C/T]TAACAATAGCTTTTA | 219333 |
rs116672111 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP12 | GRCh38.p7 | 13:27080580 | AAGGGAGAGTAAAGA[A/G]ACTTGAGAGAGGAAA | 219333 |
rs116676144 | snp | A/T | 0.0532157 | 0.154195 | intron-variant | USP12 | GRCh38.p7 | 13:27093635 | TTATCAAACTAAGTA[A/T]ACTCTTACCATACAA | 219333 |
rs116795329 | snp | A/T | 0.0168055 | 0.0901129 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27157004 | AATCTATTTGTTAAT[A/T]TCCTTACCTGTAAAA | 219333 |
rs116811477 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146426 | CACCTATGTAATAAC[A/G]CACACGGCTAAAGGC | 219333 |
rs116902525 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | USP12 | GRCh38.p7 | 13:27115617 | ACCACAACAATTATA[C/T]AGCACAAGTTTGTGA | 219333 |
rs116919580 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27100219 | AATGCAATAATCCTC[C/T]GTCCCTGAAAATAAT | 219333 |
rs116921729 | snp | C/T | 0.0876345 | 0.190099 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116879 | CTCTACCATCTAGCC[C/T]AGGTGTGCAGTAGGC | 219333 |
rs116932986 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160080 | AGAACGAAAATACCA[A/C]CTTAAATACATACCA | 219333 |
rs116940052 | snp | C/T | 0.0205541 | 0.0992701 | synonymous-codon | USP12 | GRCh38.p7 | 13:27095715 | AATATTACCATTAGG[C/T]AAACGACCATTTTGT | 219333 |
rs116950483 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160904 | CCCATCTCCCCGGGT[C/T]AAGCCCAGCATCCAT | 219333 |
rs116969880 | snp | A/C | 0.0872718 | 0.189788 | intron-variant | USP12 | GRCh38.p7 | 13:27110783 | AAAATTGTATTTGTA[A/C]TACAATCTAATCAAG | 219333 |
rs116971831 | snp | A/T | 0.0901694 | 0.192235 | intron-variant | USP12 | GRCh38.p7 | 13:27098278 | TTCTGTATGGCAAAG[A/T]CAACATAAATGAAGA | 219333 |
rs116973484 | snp | G/T | 0.0165278 | 0.0893908 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153814 | CTTCCTTATCATCTC[G/T]TTTCTTAGCCTCTCT | 219333 |
rs117003578 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165458 | ATTAATTAGTAGTGC[A/C]AATGAATACTTTTTA | 219333 |
rs117055630 | snp | G/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144747 | GTTTTGTTTTTTGTT[G/T]TTTTTTTTTTTTCCC | 219333 |
rs117102691 | snp | G/T | 0.0905309 | 0.192535 | intron-variant | USP12 | GRCh38.p7 | 13:27098472 | TAATACATGACAAGG[G/T]ACTGGGAAATAACAA | 219333 |
rs117132252 | snp | C/T | 0.0970103 | 0.197722 | intron-variant | USP12 | GRCh38.p7 | 13:27086511 | GTGATTCTCGATTTA[C/T]ATTTATCCGTATTTT | 219333 |
rs117228016 | snp | G/T | 0.0966517 | 0.197444 | intron-variant | USP12 | GRCh38.p7 | 13:27082488 | GCAATAAGGCTGTTT[G/T]GCTTTCTTATCATTT | 219333 |
rs117254740 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153788 | AATATTTACTGGGTA[C/T]TCTTTCCTGTCTTCC | 219333 |
rs117299687 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP12 | GRCh38.p7 | 13:27122451 | GGGTACATCTTTATT[A/G]GCAGTGTGGAAACGG | 219333 |
rs117337472 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141802 | TCTGAACTCCAAAAT[A/C/G]TTCCAAAATCTGACT | 219333 |
rs117378110 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | USP12 | GRCh38.p7 | 13:27097937 | CTAAACATGAAATTC[A/C]TTTGTTTCATATACA | 219333 |
rs117391359 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP12 | GRCh38.p7 | 13:27106215 | ATCCCCTGAAACGTT[A/G]CATGAAAAAGTCACC | 219333 |
rs117439802 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132309 | CTTATGAAGTAGAGA[C/G]GGGCCAGTAGAAATG | 219333 |
rs117491140 | snp | C/T | 0.0970103 | 0.197722 | intron-variant | USP12 | GRCh38.p7 | 13:27086554 | CAAAGAATATACATT[C/T]TTCATGTATTTTCTA | 219333 |
rs117496904 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | USP12 | GRCh38.p7 | 13:27095339 | ATTTCCACAACATGG[C/T]TCTATGGCCTCCTAA | 219333 |
rs117550069 | snp | A/G | 0.0818113 | 0.184966 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173706 | AATTAGCCAGGCGTA[A/G]CAGTGTACGCCTGTA | 219333 |
rs117596099 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160004 | AAAAACCTGAAAGAG[C/T]GGAATTGCGAACACT | 219333 |
rs117601997 | snp | C/T | 0.0869089 | 0.189476 | intron-variant | USP12 | GRCh38.p7 | 13:27112971 | AGGCACAATGGCTCA[C/T]GCCTGTAATCCCAGC | 219333 |
rs117608473 | snp | A/T | 0.0356815 | 0.128715 | intron-variant | USP12 | GRCh38.p7 | 13:27078256 | AAAATAATACCATTT[A/T]AAAAAATACAGTGTA | 219333 |
rs117628838 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | USP12 | GRCh38.p7 | 13:27096400 | TAATCCAGATAATCT[A/C]AAGTCCCTTCCAAAT | 219333 |
rs117634073 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | USP12 | GRCh38.p7 | 13:27107209 | ACATGCCTGTGATTC[C/T]AACTACTCAGGAGGC | 219333 |
rs117634430 | snp | C/T | 0.0966517 | 0.197444 | intron-variant | USP12 | GRCh38.p7 | 13:27082594 | CAAGAGGCCTAGCTT[C/T]CAGCCTATCTTGGCT | 219333 |
rs117671727 | snp | A/T | 0.193194 | 0.243461 | intron-variant | USP12 | GRCh38.p7 | 13:27083874 | TATATATATATATAT[A/T]TTTTTTTGAGATGAA | 219333 |
rs117695553 | snp | A/G/T | 0.0111196 | 0.0737302 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27131431 | AAAGTGCTGTAAAAC[A/G/T]TAAAGCATTATGTAA | 219333 |
rs117708260 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27165001 | AAGAAAATAAGTCCT[G/T]AAGCTAACTTGAATG | 219333 |
rs117724449 | snp | C/T | 0.0829062 | 0.185956 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168717 | TGGTTCAGGCTATAA[C/T]ACTAACTTATGAAAA | 219333 |
rs117769179 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | USP12 | GRCh38.p7 | 13:27090554 | TGTCATTAAAAAAAA[A/T]ATTTAGCCCAAAATG | 219333 |
rs117777823 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | USP12 | GRCh38.p7 | 13:27100483 | ATACTATGACCCTCA[A/G]CCCTCCTCTCTCTGA | 219333 |
rs117829013 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP12 | GRCh38.p7 | 13:27109684 | GCACTTTGGGAGGCC[A/G]AGGTGGGTGGATTAA | 219333 |
rs117881119 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | USP12 | GRCh38.p7 | 13:27080335 | TTACCATTACTGGAA[C/G]TGGCTACAGGGGAAT | 219333 |
rs117905904 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130847 | AGTCCAAAAAGATTA[C/T]ACAAGTATCACAAGT | 219333 |
rs117919793 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | USP12 | GRCh38.p7 | 13:27097803 | TGGCAATATCACTAC[A/G]TGTTGAATATCCTTT | 219333 |
rs117926682 | snp | A/C | 0.0329836 | 0.124112 | intron-variant | USP12 | GRCh38.p7 | 13:27084119 | GTTATCTTTTTAACT[A/C]CAAAAAAAATATGCA | 219333 |
rs117933472 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27118007 | AAATTCCCGGGAAAA[C/T]ATACTAGATAAATAT | 219333 |
rs117951500 | snp | C/T | 0.0970103 | 0.197722 | intron-variant | USP12 | GRCh38.p7 | 13:27087206 | GAGAATAAGCTGGGT[C/T]AACAAAAGGTGCACC | 219333 |
rs117979676 | snp | C/T | 0.0908922 | 0.192833 | intron-variant | USP12 | GRCh38.p7 | 13:27122057 | TGGTGTGGCCAGGCA[C/T]GGTGGCTCGTGCCTG | 219333 |
rs117982689 | snp | G/T | 0.0327778 | 0.123752 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139332 | TTAAAATAGTCACTC[G/T]TGGCTGGGTGTGGTG | 219333 |
rs118056995 | snp | C/T | 0.0962929 | 0.197165 | intron-variant | USP12 | GRCh38.p7 | 13:27072220 | GGGTCTTGTGTGTTA[C/T]GGGGAGAGGGTCAGA | 219333 |
rs118104983 | snp | A/G | 0.0998734 | 0.199905 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27125683 | AAGCGCAAGGGGTCA[A/G]GGGATTTCCCTTTCC | 219333 |
rs137899946 | in-del | -/TAAA | | | intron-variant | USP12 | GRCh38.p7 | 13:27110124 | GGATTTCCTTTTCCA[-/TAAA]GGTAAAAAAAAAAAA | 219333 |
rs137906765 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124085 | AATCTGGGAGATGGC[C/T]ATCCTGCAATTAAAT | 219333 |
rs137918931 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160912 | CCCGGGTTAAGCCCA[G/T]CATCCATCAGCTCTT | 219333 |
rs137938323 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP12 | GRCh38.p7 | 13:27120377 | TCTGCTCCAGGCCAG[A/G]CACAGTAGCTCACGC | 219333 |
rs137952162 | snp | C/T | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152933 | GGTGACAGAGCGAGA[C/T]TCCGTCTCAAAAAAA | 219333 |
rs138055654 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27080800 | TGCATATAAAGGTTA[C/T]GCTTATACTATACTG | 219333 |
rs138080848 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136729 | TAAAACTTGATATAT[A/G]CATTATATGGTCCAT | 219333 |
rs138087977 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124584 | ATTTTAAGTTAGATC[A/G]GGTCAGTACACAAAG | 219333 |
rs138171080 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140063 | CATTAAAAATTACAC[A/T]ATGCAACATAAAAAG | 219333 |
rs138173008 | snp | A/G | 0.111576 | 0.20818 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167211 | AGGTTGCGGTGAGCC[A/G]AGATTGCAGCATTGC | 219333 |
rs138187961 | snp | A/C | 2.21232e-05 | 0.00332582 | synonymous-codon | USP12 | GRCh38.p7 | 13:27095601 | GTATGATATACTTAC[A/C]GTTTCACAAGTAAGA | 219333 |
rs138191896 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133560 | ATGAACCTGGGAGGG[C/G]GGAGCTTGCAGTGAG | 219333 |
rs138192234 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | USP12 | GRCh38.p7 | 13:27088822 | AATCTTAGCTGTGAG[C/T]ACGCTTGGATGTTGA | 219333 |
rs138206047 | snp | A/G | 0.0228947 | 0.104514 | upstream-variant-2KB | USP12, USP12-AS2 | GRCh38.p7 | 13:27172195 | GAAGGGGTGCGGCGG[A/G]GAGGCGCGGGGGTGG | 219333 |
rs138218008 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP12 | GRCh38.p7 | 13:27093244 | ATGAAAAACAAGTCA[C/T]GGACTGGGAGAAAAT | 219333 |
rs138298175 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146222 | GCCCAGCCAACATGG[G/T]GAAACCCTGTGTCTA | 219333 |
rs138304963 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | USP12 | GRCh38.p7 | 13:27103351 | ATTCAAAAGCCAAAA[A/T]TATATTTCAAAACAT | 219333 |
rs138341940 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173317 | CTACCTGGGCCTTGT[C/T]CGAGTGTCACCATGC | 219333 |
rs138411109 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27115159 | TGAATCTCTCCAGGG[A/C/G]ATAAAGACAAAGCGT | 219333 |
rs138452226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27098481 | ACAAGGGACTGGGAA[A/G]TAACAATTAAAACAA | 219333 |
rs138460622 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155548 | CTAAAATCTGAAAAT[C/T]AAAGTAACTGTACCT | 219333 |
rs138475761 | in-del | -/AAA | | | intron-variant | USP12 | GRCh38.p7 | 13:27086175 | ATCTTTTGTCTCTTT[-/AAA]AAAAAAAAAAAAAAA | 219333 |
rs138506696 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27083221 | CTGATCATGTATCAC[C/T]GTAACAATATAATAA | 219333 |
rs138529474 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27109569 | GACACAACAATCAAA[C/T]TGCAAATGTAAATGC | 219333 |
rs138560467 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | USP12 | GRCh38.p7 | 13:27114624 | GCTGCCATAAGAGCC[A/G]TTATCTGTGACAATA | 219333 |
rs138578684 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124400 | AATACACCTTACCAA[C/G]AAATTAAAAATGATG | 219333 |
rs138605148 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | USP12 | GRCh38.p7 | 13:27080499 | ACCTGGCCATGCATG[C/G]ATCTTCTTCAATACC | 219333 |
rs138628703 | in-del | -/A | 0.0964308 | 0.19777 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27132428 | GCAGTACAGGAAGGC[-/A]AAAAAAAAAGAAAAG | 219333 |
rs138632690 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | USP12 | GRCh38.p7 | 13:27097607 | TGGTGCTATGGTTCT[A/G]CTTCTAACTGCACGC | 219333 |
rs138652562 | snp | A/C/T | 0.00517822 | 0.0506191 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161124 | TCCCAGCTACTACCC[A/C/T]CAAGGTACCACCTTA | 219333 |
rs138656590 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | USP12 | GRCh38.p7 | 13:27084335 | ACATGGTGTAACCCC[A/G]TCTCTACTAAAAATA | 219333 |
rs138723643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27121005 | CCTTTAAATTCTCTT[C/T]TAACAGCTGAATGGA | 219333 |
rs138778386 | snp | A/G | 0.021333 | 0.101051 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27173719 | TAGCAGTGTACGCCT[A/G]TAATCCCAGCTACTC | 219333 |
rs138789455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27102741 | AGTCTTCTTTTTTTC[A/G]TGACAGTGACACATT | 219333 |
rs138857958 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141162 | CTGGGACTACAGGTG[C/T]GCACCATCATGCCTG | 219333 |
rs138910969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27128643 | ATCAAGCTCTTTCTA[C/T]CATATTCTTGATAAT | 219333 |
rs138914322 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27108954 | CACAAAAAAAGATAC[A/G]TATGTGTGTGTGTGT | 219333 |
rs138986124 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137754 | TGAATTGCTTCTAAC[A/C]AGTAGAAAATGACGG | 219333 |
rs139054786 | in-del | -/A | 0.0225045 | 0.103662 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166214 | TGCTGTCAAATACAT[-/A]ACAAAATACCATATT | 219333 |
rs139162792 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | USP12 | GRCh38.p7 | 13:27110306 | ATGTGTCACAATCAT[C/T]GCAAATAAAGGACCT | 219333 |
rs139272535 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153481 | GAAATCTAGTAACAA[C/T]AAACTCCAAAAATGG | 219333 |
rs139276866 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27077349 | TAAAATGAGTGTCAG[C/T]GCACTATTAATAAAT | 219333 |
rs139309002 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP12 | GRCh38.p7 | 13:27089730 | GAGTAGAATATCATT[C/T]ACCTAGTAATACTTA | 219333 |
rs139314803 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146327 | GAATTACTTGAACCC[A/G]TGAGGCAGAGGTTGC | 219333 |
rs139324601 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | USP12 | GRCh38.p7 | 13:27070175 | TGCATCTCACAAATA[C/T]ATCAATGAGTGAATA | 219333 |
rs139355095 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27152285 | TCCACACAATGGAAC[A/C]ATATTTGTCCATTAA | 219333 |
rs139355463 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126871 | CTGTGAAAAATGTAT[A/G]GAAGATGTTCAGAAC | 219333 |
rs139373871 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27072133 | CTATGGAGGATGACA[C/T]ATCAAAACTTTTTCT | 219333 |
rs139379962 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27149681 | AAATTACAGCTCGAT[A/G]GGAGGAATAAGTTCT | 219333 |
rs139391810 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138119 | CCTTGCAGAGGGCAC[A/G]GCTTACCTACAACAG | 219333 |
rs139412716 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27076624 | CCCACTATCTAGCAA[A/C]ATGCCTGACATATGA | 219333 |
rs139413005 | snp | C/G/T | 9.93911e-05 | 0.00704888 | missense, utr-variant-5-prime, intron-variant | USP12 | GRCh38.p7 | 13:27105892 | TTTTCCCGAAATGGA[C/G/T]GACAAAAATAAAGTG | 219333 |
rs139418557 | snp | A/G | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153385 | CAATTTTGTTTTTTA[A/G]ATAAAACATATATAC | 219333 |
rs139497530 | snp | A/G | 0.00110659 | 0.0234962 | intron-variant | USP12 | GRCh38.p7 | 13:27105981 | TTTGTTAAATTTAGG[A/G]CAACACATTTTCAAG | 219333 |
rs139503084 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP12 | GRCh38.p7 | 13:27105260 | TCTAGCTCCTTCCCC[A/G]GAGTGTGGCTCCTGG | 219333 |
rs139530951 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27143326 | AGGGAGTATCACATT[G/T]ATTCCTTATTCTGAA | 219333 |
rs139565703 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146641 | ATACCTAAAATGAAC[C/T]AATTGCTACTCCCCT | 219333 |
rs139569660 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | USP12 | GRCh38.p7 | 13:27099917 | ACTAGCCTACATGGA[C/T]TTAACAACTAATCTT | 219333 |
rs139583119 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27147777 | GAAAAAAAAAATTTT[A/T]AAAAACCGTCAACCA | 219333 |
rs139688735 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158036 | TTTACTGGGTGAACT[C/G]TGTTCCCTAATAAAG | 219333 |
rs139708189 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116724 | TGCCCTACACAGGTG[C/T]GTCTTTATCCTTTAC | 219333 |
rs139734751 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP12 | GRCh38.p7 | 13:27169724 | CTGTGTCTCACTGTC[C/T]TAATCTGATTACAGC | 219333 |
rs139738908 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27091584 | ATGTCATGTCATGCA[C/T]AATATGGGGAGATCC | 219333 |
rs139758867 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27094664 | CATGAATGCATAACC[A/T]GCATCTAGTTAGGAA | 219333 |
rs139786196 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27129095 | GGAATATTCCATACA[C/T]TTCAAATAAAAAAAA | 219333 |
rs139871934 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162852 | TTTTCCTATTTTCCT[G/T]CCCTCAGAGTTTGAA | 219333 |
rs139874485 | in-del | -/G | 0.0142736 | 0.0832652 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140296 | TTAATATTGGAGCTA[-/G]TTGCATAGTACACGT | 219333 |
rs139919267 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27125215 | TATTTATCACTCTAA[A/G]TTGAAATTTTTTAAA | 219333 |
rs139944179 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27071602 | TCCAATATGATGCTT[A/G]AAACAGGCAAGGATA | 219333 |
rs139945821 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27162290 | GGACTCAAAGTCACA[C/T]ACACACAGATATGCA | 219333 |
rs139954776 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27099275 | GTATGCATGTATTAT[C/G/T]TGCATGCTTAAAAAT | 219333 |
rs139957304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27111221 | AATAAGCTGACTTTC[A/G]ATCTTTTTAATAATT | 219333 |
rs139977980 | snp | G/T | 0.0869089 | 0.189476 | intron-variant | USP12 | GRCh38.p7 | 13:27116269 | GTGAGCCGAGATCGC[G/T]CCACTGCACTCCAGC | 219333 |
rs139987505 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27167354 | AGTTTTTATATTTTC[C/T]AGATTTTCTATGAGA | 219333 |
rs140035222 | in-del | -/CA | 0.0509478 | 0.151255 | intron-variant, upstream-variant-2KB | USP12 | GRCh38.p7 | 13:27116786 | AGATATGTTCAGATG[-/CA]CACACTTATTCCTGT | 219333 |
rs140067567 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | USP12 | GRCh38.p7 | 13:27094116 | ATGCTAAATCTTGGG[C/T]GAGATTTTGATGAGG | 219333 |
rs140076288 | snp | C/T | 0.000513956 | 0.0160223 | missense | USP12 | GRCh38.p7 | 13:27095719 | TTACCATTAGGTAAA[C/T]GACCATTTTGTTTTT | 219333 |
rs140109247 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27119975 | GTACACTCCTCTCTC[C/T]AGCCTAACGCTAACT | 219333 |
rs140153708 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP12 | GRCh38.p7 | 13:27090855 | AAATTATTATTAGCA[C/T]ATAGAGTTGTTCATC | 219333 |
rs140166336 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27130350 | TCATAGCTGTCCAGA[G/T]ATAGTAAGACAGAAA | 219333 |
rs140185078 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133883 | GTGCCTGTAATCCCA[A/G]CCCTTTGGGAGGTCA | 219333 |
rs140214676 | in-del | -/GAAC | | | intron-variant | USP12 | GRCh38.p7 | 13:27102014 | TTCCCATTTTTTAAT[-/GAAC]GAATGAATGAATGAA | 219333 |
rs140229488 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | USP12 | GRCh38.p7 | 13:27083257 | AAGTTTGAAATAGTG[A/C]AAGAATTACCAAAAA | 219333 |
rs140243624 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163521 | CATTACTTATACCAA[C/T]AAGAAAAACATCTCA | 219333 |
rs140247885 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27087083 | AGAGGGGGAAGTCAA[A/C]GCAGAGGGGAAGGGG | 219333 |
rs140287812 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138551 | GTGACCACTGGAGAG[C/G]TTAGATAAGCACCTC | 219333 |
rs140326384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142544 | CGAATGTACACACAA[A/G]TATACATTTGTCAAG | 219333 |
rs140336406 | snp | A/C | 0.000798403 | 0.0199641 | downstream-variant-500B | USP12 | GRCh38.p7 | 13:27066123 | TAAATACATTTTAGG[A/C]AAAAAGGAAAAAACA | 219333 |
rs140416562 | snp | G/T | 0.451359 | 0.148171 | intron-variant | USP12 | GRCh38.p7 | 13:27079216 | CGTGCTCCCTGTGTG[G/T]GGCGGGGGGGAGTGG | 219333 |
rs140473511 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27145209 | ATTTCCCAGTGAGTT[G/T]CCTTCTTGAAGAATG | 219333 |
rs140508923 | snp | G/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27103058 | AATTAAAATCAGTTC[G/T]TTCCAGGACCATCAA | 219333 |
rs140549287 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | USP12 | GRCh38.p7 | 13:27107716 | TGATACAAGATCTGC[A/G]ATAAGAAATGTACAA | 219333 |
rs140565928 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | USP12 | GRCh38.p7 | 13:27081685 | AGGAATCTCAATCTA[C/T]GGCAGCTGTAGACTT | 219333 |
rs140723717 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155288 | GGGTTTCACCATGTT[A/G]GCCAAGATGGTCTTG | 219333 |
rs140738758 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27161681 | TTTGAGACCAGCCTG[A/G]GCAACATGGTGAAAC | 219333 |
rs140787450 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27125399 | CTATGTCACAACACA[C/G]GATGTACTATAGCAA | 219333 |
rs140800434 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP12 | GRCh38.p7 | 13:27170144 | ATGCTTTCCTAAAAT[G/T]TAAACTGTGAGAAAG | 219333 |
rs140800496 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124210 | TAAACTAACAACCAG[A/G]AATGTTTTCAAGAAA | 219333 |
rs140837793 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27127812 | ATGATTAATCACTGC[A/G]CAAGTAACTGCAAAT | 219333 |
rs140856906 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27139788 | TGATTCACATATTTA[C/T]TTTAAAAACATTTTC | 219333 |
rs140864331 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27164555 | ATCACAAAAGTCTTC[A/G]AGTTTTGCTGTGAGA | 219333 |
rs140965277 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27108742 | CAGGTGGATCAGTTG[C/T]GGTCAGGAGTTTAAG | 219333 |
rs140967288 | in-del | -/A | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160430 | AGCCTCCTCAAATTG[-/A]AAAAAAAAAATGCAA | 219333 |
rs141053458 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27151879 | AAGATACACAAATGG[A/C]CAATAAGTACCTAAA | 219333 |
rs141099877 | in-del | -/A | | | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124310 | AACCAGATTATGGCT[-/A]AAAAAATGGTGTCTA | 219333 |
rs141102299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27086505 | TTTATAGTGATTCTC[A/G]ATTTACATTTATCCG | 219333 |
rs141126961 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067220 | TCTATCTTTCTTAAA[C/T]ATGTTGATATAGCTA | 219333 |
rs141201587 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12 | GRCh38.p7 | 13:27096166 | AATATTTCAACTTGG[C/T]AAGCTTTAAAGCAGA | 219333 |
rs141212406 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27140309 | TAGTTGCATAGTACA[C/T]GTGTAGTTTGTCTGA | 219333 |
rs141245020 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27166835 | TAATCATTAAACATA[G/T]AACCTGTCAACGCCC | 219333 |
rs141247670 | snp | C/T | 0.0162398 | 0.0886349 | utr-variant-3-prime | USP12 | GRCh38.p7 | 13:27067951 | AAACCCCCAACAGAA[C/T]GAAGTCTTAGCAAAC | 219333 |
rs141251912 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144862 | CCCAGGAGTTCGAGA[C/T]CAGCCCGGGTAATAG | 219333 |
rs141265831 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant, upstream-variant-2KB | USP12, USP12-AS1 | GRCh38.p7 | 13:27124478 | AGCCAAACTATTAGT[G/T]TCCACACAACTTTAA | 219333 |
rs141269588 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27153345 | AAGCTTAGTGTCCAA[A/C]ACTCAAATTCACTTT | 219333 |
rs141330214 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27136086 | ATTACAATAAAGTAA[A/G]CCGCTTTCCATGTTC | 219333 |
rs141372386 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138855 | AACAGAGAAACCCAT[A/G]TTCACCCTGTAACAG | 219333 |
rs141485053 | in-del | -/TTTC | 0.478536 | 0.101348 | intron-variant | USP12 | GRCh38.p7 | 13:27085161 | TGGAATGTTTTCTTT[-/TTTC]TTTCTTTCTTTCTTT | 219333 |
rs141554448 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | USP12 | GRCh38.p7 | 13:27104091 | CAAGCTGGAGAGTGG[C/G]GCAATCAGGGCTCAC | 219333 |
rs141585368 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP12 | GRCh38.p7 | 13:27080677 | ACAGAAATACAGGCA[C/T]ATCTTGGACACGCAG | 219333 |
rs141591841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27155822 | GATGCGGAAAAGGTT[C/T]AACTTAATTTGTAAA | 219333 |
rs141601471 | in-del | -/ATAT | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27148684 | AAAAAATTATATATA[-/ATAT]TATATATAATATAAA | 219333 |
rs141647907 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27080232 | AAGACTTGCATGGGG[A/G]TGTGTGTGCCAACAG | 219333 |
rs141662350 | snp | A/G | 1.68698e-05 | 0.00290424 | intron-variant | USP12 | GRCh38.p7 | 13:27071032 | AAAAGCAACATATGC[A/G]TACAACTTTCAAAAA | 219333 |
rs141702941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27146777 | CTAAATAAAGATAAA[C/T]TGAACTCCTAATCTT | 219333 |
rs141750766 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | USP12 | GRCh38.p7 | 13:27083837 | TTCTTCAGTGTTCTC[A/G]GGATGAACCTTTTTG | 219333 |
rs141763533 | snp | C/T | | | intron-variant | USP12 | GRCh38.p7 | 13:27076238 | CCATATTAAGAAAAA[C/T]GACAATGTATATCCT | 219333 |
rs141784939 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27113473 | GTGACATTTTAGAAC[A/T]TTGTATTTCCACATC | 219333 |
rs141785016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27158426 | TGTTACAGGCATGCA[C/T]CACTTAATGACAGGG | 219333 |
rs141838205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27093939 | TCCAAACAGGCTGCA[C/T]ACTATATGATTTCAA | 219333 |
rs141989119 | in-del | -/AT | 0.0391387 | 0.134304 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27133245 | ACTCACCACACTCAC[-/AT]GACATCTTTCTGTTA | 219333 |
rs141995227 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP12 | GRCh38.p7 | 13:27098118 | CAGAAAGTAAAGTTG[C/T]TACTACCTCAGCCAC | 219333 |
rs142030631 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27142426 | AACTGATTAAATTTT[A/T]AAAATATGCTGTGCA | 219333 |
rs142054250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27095585 | TTCTCTATACAAAAT[C/T]GTATGATATACTTAC | 219333 |
rs142120111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27137827 | AGACTCCATACTGCT[A/G]GCAGACTTGCTCCCT | 219333 |
rs142156788 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP12 | GRCh38.p7 | 13:27094290 | AGGTGGGTTACTTGA[C/G]GGCAGGAGTTCAAGA | 219333 |
rs142157988 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | USP12 | GRCh38.p7 | 13:27096809 | ATTTAGGACATTTTA[G/T]TTTTAGATCCTCAAT | 219333 |
rs142158131 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP12 | GRCh38.p7 | 13:27100623 | ATGCACCTCAATCCC[A/G]TACAATTCAAGAACC | 219333 |
rs142158598 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27141347 | AACATTTCCTTGCTA[G/T]GTCCACTAAAAGGAA | 219333 |
rs142229276 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP12, USP12-AS2 | GRCh38.p7 | 13:27172536 | AGAAAGATAAGTAAT[A/G]GGGGAAGGAGAGGAG | 219333 |
rs142236928 | in-del | -/AAA | | | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27163783 | AAAAAAAAAAAAAAA[-/AAA]AAGAAAAAAAAAAAA | 219333 |
rs142243298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27144148 | GCTGAAGTTGGAGCC[A/G]AGACTGCACCACTGC | 219333 |
rs142282572 | snp | A/C/G | 0.00358923 | 0.042236 | intron-variant | USP12 | GRCh38.p7 | 13:27122264 | CCCCATACTGTTCTC[A/C/G]TGGTAGTGAATACGT | 219333 |
rs142385966 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27168765 | TCACATGTAAGCACA[A/C]CACTAGTGATCTAAA | 219333 |
rs142394652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP12 | GRCh38.p7 | 13:27078132 | TTTGGATGAATTTCT[A/G]TTATTCACTTGGCCC | 219333 |
rs142405785 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27126383 | CAGACCTGCAGCTGA[A/G]GGGCCTGTGAGAAGG | 219333 |
rs142417414 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP12 | GRCh38.p7 | 13:27120416 | CCAACACTTTGAGAC[A/G]ATGAGGCAGGTGGAT | 219333 |
rs142426104 | snp | C/T | 8.25375e-05 | 0.00642355 | synonymous-codon, utr-variant-5-prime, intron-variant | USP12 | GRCh38.p7 | 13:27105867 | AGGTTGACTCTTATA[C/T]GCAAGAACTTTTTCC | 219333 |
rs142502034 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27134528 | AGAGTTACTTTCTAA[A/T]CAGGTCCCCTAAAGT | 219333 |
rs142520776 | snp | A/G | | | intron-variant | USP12 | GRCh38.p7 | 13:27091990 | TGTGCATACACATAC[A/G]ATAACACACTGTACT | 219333 |
rs142585115 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP12 | GRCh38.p7 | 13:27116129 | CATCCTGGCTAACAC[A/G]GTGAAACCCTGTCTC | 219333 |
rs142587104 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27160991 | TAGCGTTCCCCTCCA[C/G]AAAGCGTCATCTTTC | 219333 |
rs142598898 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP12, USP12-AS1 | GRCh38.p7 | 13:27138967 | GTGTCACAGTTTCAA[C/T]GGTAAGGTGTATGAT | 219333 |
rs142648059 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | USP12 | GRCh38.p7 | 13:27077105 | TCAAACATAACCGAG[C/T]GTTGTACAACTTAAA | 219333 |