SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs11221 | snp | A/G | 0.0486741 | 0.148216 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:211865 | TTTAAAATAAATTGT[A/G]ATCAATAATAGTACC | 9097 |
rs16428 | in-del | -/AGAG | 0.460142 | 0.135426 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:211910 | AATCCACAGTACATC[-/AGAG]AGAGACACAATAATA | 9097 |
rs471274 | snp | G/T | 0.456717 | 0.140599 | intron-variant | USP14 | GRCh38.p7 | 18:203081 | TGAGGAGACAAAATG[G/T]AAAGAAATCCCATTA | 9097 |
rs477066 | snp | C/T | 0.462253 | 0.132093 | intron-variant | USP14 | GRCh38.p7 | 18:159281 | AATCCAATGCAACGT[C/T]TGATGAAACGAAAAC | 9097 |
rs477718 | snp | A/C | 0.22263 | 0.248497 | intron-variant | USP14 | GRCh38.p7 | 18:186210 | ctcatgcctgtgatc[A/C]cagtgctttgggagg | 9097 |
rs478326 | snp | A/G | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:181055 | TACGTGTGCTGTAAC[A/G]TGAATGAACCATGAA | 9097 |
rs479140 | snp | A/C/G | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:180991 | TACGTGTGCTGTAAC[A/C/G]TGAATGAACCATGAA | 9097 |
rs479167 | snp | A/T | 0.277778 | 0.248452 | intron-variant | USP14 | GRCh38.p7 | 18:180979 | aacatgaatgaacca[A/T]gaaatactattcagc | 9097 |
rs485211 | snp | C/T | 0.222928 | 0.24853 | intron-variant | USP14 | GRCh38.p7 | 18:166277 | TATTGTGTTACCTTA[C/T]GCAGTTGAAGCAAAT | 9097 |
rs489560 | snp | A/G | 0.462034 | 0.132445 | intron-variant | USP14 | GRCh38.p7 | 18:165098 | GGATAACAGGTCACC[A/G]CCACCATGCGTGACA | 9097 |
rs489577 | snp | A/T | 0.465052 | 0.127485 | intron-variant | USP14 | GRCh38.p7 | 18:177101 | TTAGGTGCTTTTTTT[A/T]AAAATATCCTTAAGT | 9097 |
rs490425 | snp | A/C | 0.462363 | 0.131916 | intron-variant | USP14 | GRCh38.p7 | 18:165022 | GGCGCCATCTCGGCT[A/C]ACTGCAACCACCGCC | 9097 |
rs493422 | snp | C/T | 0.269809 | 0.249214 | intron-variant | USP14 | GRCh38.p7 | 18:202494 | AGCCCAAGAAACTCC[C/T]GTTCTTTACGTTTTA | 9097 |
rs495284 | snp | C/T | 0.0865458 | 0.189163 | intron-variant | USP14 | GRCh38.p7 | 18:177063 | GGAAGACATGACAAG[C/T]TCTGGACTTGAAAAA | 9097 |
rs499571 | snp | A/T | 0.0711525 | 0.174681 | intron-variant | USP14 | GRCh38.p7 | 18:189598 | agtgattctcctacc[A/T]cagcctcctgagtag | 9097 |
rs499634 | snp | A/C | 0 | 0 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212564 | agctgagatcacacc[A/C]ctgcactccagcctg | 9097 |
rs503086 | snp | A/C | 0 | 0 | synonymous-codon | USP14 | GRCh38.p7 | 18:197672 | ACAGAAATTGGAAGC[A/C]ATAGAGGATGATTCT | 9097 |
rs505610 | snp | C/T | 0.19334 | 0.243495 | intron-variant | USP14 | GRCh38.p7 | 18:173718 | GTGAGCCACCGCACC[C/T]GGTCTATTATCTGTT | 9097 |
rs507184 | snp | A/G | 0.222333 | 0.248464 | intron-variant | USP14 | GRCh38.p7 | 18:186998 | TAGTTTGACCTTTCA[A/G]ATATTGGCAGTTGTT | 9097 |
rs511573 | snp | C/T | 0.260227 | 0.249791 | intron-variant | USP14 | GRCh38.p7 | 18:175140 | agttaatttttataa[C/T]tgactttgtatcctg | 9097 |
rs511859 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | USP14 | GRCh38.p7 | 18:193365 | TTGGACATTTTAATA[C/T]TGTTAAATCTTTGGG | 9097 |
rs513271 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:171604 | gttttgagagacata[A/T]acgagatgaatgttg | 9097 |
rs513402 | snp | C/T | 0.474634 | 0.109726 | intron-variant | USP14 | GRCh38.p7 | 18:184704 | GCCTGGGAGGTCGAG[C/T]CTGCAGTGAGCCATC | 9097 |
rs516905 | snp | A/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:164428 | CGTTAATGGGTAGGA[A/T]GCAATAAAGGCCAAA | 9097 |
rs523239 | snp | A/G | 0.462253 | 0.132093 | intron-variant | USP14 | GRCh38.p7 | 18:162039 | GTATCTCATATAACC[A/G]GAATCATCCATGTTG | 9097 |
rs541733 | snp | A/G | 0.261332 | 0.249743 | intron-variant | USP14 | GRCh38.p7 | 18:172410 | gttgttgaaatgaca[A/G]taaaggatttaaaat | 9097 |
rs544730 | snp | G/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:164415 | TTCATTTTTTTTTTT[G/T]GGCCTTTATGGCTTC | 9097 |
rs545447 | snp | C/T | 0.496999 | 0.0386216 | intron-variant | USP14 | GRCh38.p7 | 18:208222 | atttacaaaaacaaa[C/T]acaatatgaaataga | 9097 |
rs545684 | snp | A/G | 0.269538 | 0.249235 | intron-variant | USP14 | GRCh38.p7 | 18:159382 | GATTGGCGTTTGACA[A/G]GGGCTTGTATTGTTT | 9097 |
rs551835 | snp | A/G | 0.236434 | 0.249632 | intron-variant | USP14 | GRCh38.p7 | 18:160887 | AGCCTTTCAGGAATT[A/G]CACATTGCCTACAAC | 9097 |
rs553212 | snp | C/T | 0.266546 | 0.249452 | intron-variant | USP14 | GRCh38.p7 | 18:195405 | TGGGTTCAGTCTGTA[C/T]AATGATGATAGGTGA | 9097 |
rs557249 | snp | A/C | 0.4582 | 0.138394 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:156739 | atatgcactgggaaa[A/C]caaaaactttgtgtg | 9097 |
rs562117 | snp | G/T | 0.221737 | 0.248397 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157065 | tttgtttgtttgttt[G/T]gagacagggtctcac | 9097 |
rs562748 | snp | A/G | 0.261608 | 0.24973 | intron-variant | USP14 | GRCh38.p7 | 18:167536 | catacgtgagagtga[A/G]accctgtctcaaaaa | 9097 |
rs563155 | snp | C/T | 0.296364 | 0.245663 | synonymous-codon | USP14 | GRCh38.p7 | 18:166819 | CATCAAAATAAAAAA[C/T]GTAAGTATTATCTTA | 9097 |
rs565653 | snp | A/G | 0.22263 | 0.248497 | intron-variant | USP14 | GRCh38.p7 | 18:171973 | tggccaggcatggtg[A/G]ctcactcctataatc | 9097 |
rs566693 | snp | A/C | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:188939 | cggctttggcctccc[A/C]aagtgctgggattac | 9097 |
rs566748 | snp | A/T | 0.219947 | 0.248187 | intron-variant | USP14 | GRCh38.p7 | 18:199557 | caacaaaaagcagaa[A/T]tttttttttaaaaca | 9097 |
rs567685 | snp | A/C | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:189044 | TTTATATTTTCCTAC[A/C]AAATTGTCCTGTCTT | 9097 |
rs569449 | snp | G/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:189200 | tagttttcaaagaat[G/T]ggctattagatttgt | 9097 |
rs572981 | snp | A/G | 0.19459 | 0.243782 | intron-variant | USP14 | GRCh38.p7 | 18:206874 | GGGCAATGTTGCCCA[A/G]ACTGGAGGGCAGTGG | 9097 |
rs574176 | snp | A/G | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:180923 | TGTGCTGTAACGTGA[A/G]TGAACCATGAAATAC | 9097 |
rs575268 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | USP14 | GRCh38.p7 | 18:185110 | TCTCAATATACACAG[C/T]GTTAACAGTTACTAG | 9097 |
rs575847 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:206534 | taaaaattaaaaaaa[A/C]ctttcttctgcaaaa | 9097 |
rs579219 | snp | C/T | 0.455263 | 0.142713 | intron-variant | USP14 | GRCh38.p7 | 18:193162 | TTGATTTGTATAATA[C/T]ATATCTTTGGGGTTG | 9097 |
rs584429 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:188955 | aagtgctgggattac[A/C]ggcgtgagccaccgt | 9097 |
rs585578 | snp | C/T | 0.41833 | 0.184838 | intron-variant | USP14 | GRCh38.p7 | 18:204232 | TGTGAAAATAATGGA[C/T]CTCCCAAACTGGAAT | 9097 |
rs585614 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:204209 | ACTGGAATAAACTTA[C/T]GGTTTTTTTTTTTTA | 9097 |
rs585699 | snp | G/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:189229 | gttcattcaattttt[G/T]gagttgtctgattca | 9097 |
rs586720 | snp | A/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:189497 | tttttctttgttttt[A/T]ttttgagaaggagtc | 9097 |
rs598119 | snp | G/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:185354 | agtagagacgggttt[G/T]gctatattgtcaagg | 9097 |
rs605049 | snp | C/T | 0.284995 | 0.247539 | intron-variant | USP14 | GRCh38.p7 | 18:209430 | TTAGGAGGAACTCAC[C/T]GCTTCAACTCATTTT | 9097 |
rs617421 | snp | C/T | 0.27008 | 0.249192 | intron-variant | USP14 | GRCh38.p7 | 18:208998 | TATAGTGGCTTACGC[C/T]GGGGCGAGTGGATCA | 9097 |
rs634810 | snp | G/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:185330 | tgcctgactaatttt[G/T]gtatttttagtagag | 9097 |
rs640525 | snp | A/C | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:197911 | TCAAAAAACATTACC[A/C]AAAATCAACAATGAA | 9097 |
rs647843 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:189123 | taacaaataagaaat[A/T]aaaataccaaaaaaa | 9097 |
rs652079 | snp | A/G | 0.223819 | 0.248625 | intron-variant | USP14 | GRCh38.p7 | 18:196098 | gaggccgaggctggc[A/G]gatcacaaggtcagg | 9097 |
rs655781 | snp | A/G | 0.430136 | 0.173352 | intron-variant | USP14 | GRCh38.p7 | 18:196829 | TTTCCTACATTTACC[A/G]TACTTACTGGAACAT | 9097 |
rs668734 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:196170 | tgcctggctaatttt[G/T]gcattttttttagta | 9097 |
rs670078 | snp | A/C | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:195876 | TTTGTTTGGGAAGAC[A/C]AAGGCTGGCCAGAAG | 9097 |
rs681760 | snp | G/T | 0.267091 | 0.249415 | intron-variant | USP14 | GRCh38.p7 | 18:195644 | AATTCTTAGTAGTTT[G/T]GGTTCTTAGCTGTCC | 9097 |
rs683635 | snp | A/C | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:195212 | TTTTATACACTACTC[A/C]AAAAAACAGATGATT | 9097 |
rs684076 | snp | G/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:195129 | atctatatttcttcT[G/T]GACCTTTTTCTTTCA | 9097 |
rs684100 | snp | A/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:195112 | gaagaaatatagatt[A/T]aaagagactaataag | 9097 |
rs684978 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:194938 | actgtctcaaaaaac[A/C]aacttttttttagaa | 9097 |
rs688023 | snp | C/T | 0.239614 | 0.249784 | downstream-variant-500B | USP14 | GRCh38.p7 | 18:213827 | TCTTGTGACATTCAA[C/T]TGAGATATATGTGAA | 9097 |
rs692846 | snp | C/T | 0.192401 | 0.243274 | intron-variant | USP14 | GRCh38.p7 | 18:182139 | TTTCCTTTCATACGA[C/T]GGTATAAAAACAAAA | 9097 |
rs948263 | snp | C/T | 0.466515 | 0.124985 | intron-variant | USP14 | GRCh38.p7 | 18:165503 | CAGTTTCATTTAATT[C/T]GCATACTTCTATAAT | 9097 |
rs1061599 | snp | A/C | 0.349233 | 0.229462 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212756 | GTTCCAGGACCCTTG[A/C]CTGATGCTAGGGAAA | 9097 |
rs1274275 | snp | C/T | 0.454061 | 0.144427 | intron-variant | USP14 | GRCh38.p7 | 18:188526 | ttttttttttttttt[C/T]ctttGTGAGGGTTTG | 9097 |
rs1274276 | snp | A/G | 0.219648 | 0.248151 | intron-variant | USP14 | GRCh38.p7 | 18:188570 | GCTAGCTCTATGTCT[A/G]TCTTTTCCTGGAACT | 9097 |
rs1299113 | snp | A/G | 0.499673 | 0.0127754 | intron-variant | USP14 | GRCh38.p7 | 18:196465 | GAAGGCGGAGGTTGC[A/G]GTGAGCCGAGATCGC | 9097 |
rs1614227 | snp | C/T | 0.000173052 | 0.00930033 | intron-variant | USP14 | GRCh38.p7 | 18:180227 | TTTTTTTTTTTTTTT[C/T]CCAACTAGATGGAGT | 9097 |
rs1620545 | snp | G/T | 0.00475057 | 0.0485048 | intron-variant | USP14 | GRCh38.p7 | 18:179403 | ATTTAAACTACTCTT[G/T]GACCCTGTTTTCTCA | 9097 |
rs1784371 | snp | A/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:177498 | AATGATCTTATAAAA[A/T]GTCTATGTAGAAATA | 9097 |
rs1784372 | snp | A/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:177582 | CTAATTTCCTAATTT[A/T]AATCATCATCTGGAT | 9097 |
rs1784375 | snp | A/G | 0.261332 | 0.249743 | intron-variant | USP14 | GRCh38.p7 | 18:162214 | AACATGGGTGTACAA[A/G]TATCTGTTTGAGTCC | 9097 |
rs1784376 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:162855 | caggctggagtgcag[G/T]ggcgtgatcttggct | 9097 |
rs1784380 | snp | C/T | 0.429837 | 0.173662 | intron-variant | USP14 | GRCh38.p7 | 18:168389 | gaaatctgaaagtca[C/T]gaatattgaaaaggg | 9097 |
rs1784381 | snp | C/T | 0 | 0 | missense | USP14 | GRCh38.p7 | 18:196657 | AGAGATTTGTTTGAT[C/T]CCATGGATAAAACTT | 9097 |
rs1784384 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:189501 | tctttgttttttttt[G/T]gagaaggagtctcac | 9097 |
rs1784830 | snp | G/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:188457 | TTTAAAAGGATTTTT[G/T]GGGGTCATTTGTTAG | 9097 |
rs1785048 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:162866 | gcaggggcgtgatct[G/T]ggctcactgcaacct | 9097 |
rs1785049 | snp | A/C | 0.462144 | 0.132269 | intron-variant | USP14 | GRCh38.p7 | 18:166542 | TTCTTTATATTGGTC[A/C]GGCTGGTTTCGAACT | 9097 |
rs1785050 | snp | A/G | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:180927 | TACGTGTGCTGTAAC[A/G]TGAGTGAACCATGAA | 9097 |
rs1785051 | snp | A/T | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:180915 | AACGTGAGTGAACCA[A/T]GAAATACTATTCAGC | 9097 |
rs1785052 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:177632 | AAAAAAAAAAAAAAC[A/G]GGGGGGGAAAAATGA | 9097 |
rs1785053 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:177628 | AAAAAAAAAACGGGG[A/G]GGGAAAAATGATAGC | 9097 |
rs1785054 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:177578 | AGATGATGATTTAAA[A/T]TAGGAAATTTAGTTC | 9097 |
rs2027675 | snp | A/G | 0.344147 | 0.231595 | intron-variant | USP14 | GRCh38.p7 | 18:161922 | TACGTATACAGTTCT[A/G]TAGCATTAAATATAT | 9097 |
rs2155529 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:204792 | ATACAAAGTATAGTT[C/T]TGAAGGAAAAATGAA | 9097 |
rs2276062 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | USP14 | GRCh38.p7 | 18:193108 | GTGAAAAATAATCTT[C/T]GGATTTTTTTGGATT | 9097 |
rs2509312 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:196490 | gatcgcgccactgca[A/C]tccagcctgggcaac | 9097 |
rs2509447 | snp | C/T | 0.461923 | 0.132621 | intron-variant | USP14 | GRCh38.p7 | 18:170346 | ttgaacacttagagg[C/T]cactgtagggttatt | 9097 |
rs2846335 | snp | A/G | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:196902 | GCTGTCTCTTGCCTG[A/G]AGCCGCACAGTAGTC | 9097 |
rs2846610 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:188507 | CTGTCTCCCTCTGGG[C/T]TTTTTTTTTTTTTTT | 9097 |
rs3016613 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:196511 | cctgggcaacggacc[A/C]agactccatctcaaa | 9097 |
rs3016709 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:196568 | GCGACTGTAAATTAA[A/T]TTTAATTAATACAAA | 9097 |
rs3132798 | snp | A/T | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:180851 | GCTGAATAGTATTTC[A/T]TGGTTCATTCACGTT | 9097 |
rs3211364 | snp | C/T | 0 | 0 | downstream-variant-500B | USP14 | GRCh38.p7 | 18:213785 | TTCTGCTACTACTAC[C/T]TAGTGCTTTGCTGTG | 9097 |
rs3765617 | snp | A/G | 0.208169 | 0.246476 | intron-variant | USP14 | GRCh38.p7 | 18:202577 | TTTGTTATATAAAAT[A/G]CAATATAAAATTCTC | 9097 |
rs3835313 | in-del | -/A | | | intron-variant | USP14 | GRCh38.p7 | 18:202627 | GGGCATAGCTAAAAA[-/A]GAGCAAACAGTATTT | 9097 |
rs3859369 | snp | G/T | 0.0543475 | 0.155628 | intron-variant | USP14 | GRCh38.p7 | 18:180069 | AAGTAAACTTTTTTT[G/T]GGGGGAAATAAAACT | 9097 |
rs3859374 | snp | A/G | 0.203267 | 0.245593 | intron-variant | USP14 | GRCh38.p7 | 18:184707 | TGGGAGGTCGAGTCT[A/G]CAGTGAGCCATCAGT | 9097 |
rs3889860 | snp | A/G | 0.246769 | 0.249979 | intron-variant | USP14 | GRCh38.p7 | 18:184476 | GGAGGTATGGGTCcc[A/G]agtgtgatggctcac | 9097 |
rs4570948 | snp | C/T | 0.387263 | 0.208947 | intron-variant | USP14 | GRCh38.p7 | 18:158915 | CAGGGGAGCGCCGTC[C/T]CCCTGAGCCACCGAT | 9097 |
rs4570949 | snp | C/T | 0.387263 | 0.208947 | intron-variant | USP14 | GRCh38.p7 | 18:158917 | GGGGAGCGCCGTCCC[C/T]CTGAGCCACCGATGG | 9097 |
rs4797049 | snp | A/G | 0.200182 | 0.244986 | intron-variant | USP14 | GRCh38.p7 | 18:167583 | tggtcatggctcgct[A/G]cagctttaaactccc | 9097 |
rs4797050 | snp | A/G | 0.461481 | 0.133325 | intron-variant | USP14 | GRCh38.p7 | 18:176233 | ctttctttctacttC[A/G]Gttttaaatttttta | 9097 |
rs6505930 | snp | C/T | 0.466618 | 0.124806 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157275 | attgactcttccttt[C/T]atgaaagttttccct | 9097 |
rs7227809 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP14 | GRCh38.p7 | 18:171103 | tttaaagaaagaagc[A/G]atctctgtaacataa | 9097 |
rs7228542 | snp | C/T | 0.261332 | 0.249743 | intron-variant | USP14 | GRCh38.p7 | 18:176376 | gaggctgaccttgag[C/T]acctaggctcaagca | 9097 |
rs7230340 | snp | C/G | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:194368 | GCATCATATATGCGG[C/G]TAATAGTATTGATGC | 9097 |
rs7231900 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | USP14 | GRCh38.p7 | 18:178007 | ATAATTTTATTAGtg[C/T]ttgtttgtttgtttg | 9097 |
rs7238132 | snp | C/T | 0.461923 | 0.132621 | intron-variant | USP14 | GRCh38.p7 | 18:169217 | ccaacatggtgaaac[C/T]ccgtctctattaaaa | 9097 |
rs7238463 | snp | A/C | 0.461923 | 0.132621 | intron-variant | USP14 | GRCh38.p7 | 18:169441 | TATGAAAGACCGTTA[A/C]ATTTTGTTAAGTGTT | 9097 |
rs7241427 | snp | A/G | 0.461923 | 0.132621 | intron-variant | USP14 | GRCh38.p7 | 18:168994 | aggcaggagaatggc[A/G]tgagcctgggaggca | 9097 |
rs7241651 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | USP14 | GRCh38.p7 | 18:177503 | TCTTATAAAATGTCT[A/G]TGTAGAAATAAAAGG | 9097 |
rs8087611 | snp | A/G | 0.330947 | 0.236533 | intron-variant | USP14 | GRCh38.p7 | 18:181909 | gtatggtgggaggga[A/G]ggaggtatttgccta | 9097 |
rs8092642 | snp | A/G | 0.253544 | 0.249975 | intron-variant | USP14 | GRCh38.p7 | 18:168655 | ggccaggctggtctc[A/G]aactcctgacctcaa | 9097 |
rs9303891 | snp | A/C | 0.273856 | 0.248859 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213151 | TGCTTGTAACTTTGC[A/C]AAGTCTTTTTTATTC | 9097 |
rs9675521 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:208576 | aattttgatacatgg[G/T]atttttattttcatt | 9097 |
rs9945351 | snp | A/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:171025 | aaaaaaaaaaaaaaa[A/T]atatatatatatata | 9097 |
rs9945792 | snp | A/G | 0.256619 | 0.249912 | intron-variant | USP14 | GRCh38.p7 | 18:208856 | gttcaagcaattctc[A/G]tgcctcagcgtcccg | 9097 |
rs9947557 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | USP14 | GRCh38.p7 | 18:173301 | tttttttagtagaga[C/T]ggggtttcaccatgt | 9097 |
rs9947791 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | USP14 | GRCh38.p7 | 18:173526 | aagagattctcctgc[C/G]tcagcctcctgagta | 9097 |
rs9951575 | snp | A/G | 0.284995 | 0.247539 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213592 | GGCCATCATCTCAAC[A/G]TTAGAGTTGTGCTAG | 9097 |
rs9951626 | snp | A/G | 0.0146672 | 0.084371 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213606 | CATTAGAGTTGTGCT[A/G]GATTACTGCTTGACT | 9097 |
rs9956319 | snp | A/G | 0.150333 | 0.229274 | intron-variant | USP14 | GRCh38.p7 | 18:199462 | gatacacacagtccc[A/G]tctgaggtcaaacaa | 9097 |
rs9960992 | snp | A/T | 0.0209421 | 0.100162 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157932 | atatatatatataaa[A/T]atatataaatatata | 9097 |
rs9962773 | snp | A/T | 0.256061 | 0.249927 | intron-variant | USP14 | GRCh38.p7 | 18:194055 | ttcccccagaagggt[A/T]tgagggttctgattt | 9097 |
rs9964035 | snp | G/T | 0.460925 | 0.134204 | intron-variant | USP14 | GRCh38.p7 | 18:186741 | TGGGTGACAGAGGGA[G/T]ACTGTGTCTCAAAAA | 9097 |
rs9965109 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | USP14 | GRCh38.p7 | 18:207370 | attgacggggattac[A/G]cggaatctgtggatc | 9097 |
rs9967051 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | USP14 | GRCh38.p7 | 18:182253 | GTAACTTAAAAAATA[C/T]GTAACTTAATTCTGA | 9097 |
rs10502287 | snp | C/G | 0.188946 | 0.24243 | intron-variant | USP14 | GRCh38.p7 | 18:159885 | GAAGGAACTCAAGTA[C/G]ATTTCTAAGGTCCCT | 9097 |
rs10676245 | in-del | -/GTA | 0.453087 | 0.145793 | intron-variant | USP14 | GRCh38.p7 | 18:195381 | TTGTGCTAAGATGCT[-/GTA]GTATTTGGTGGGTTC | 9097 |
rs11336218 | in-del | -/A | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:169382 | AAAAAAAAAAAAAAA[-/A]GAGTGGACATCTTGT | 9097 |
rs11438659 | in-del | -/T | 0.485664 | 0.0834419 | intron-variant | USP14 | GRCh38.p7 | 18:177633 | TTTTTTTTTTTTTTT[-/T]AAATCTCCACTTCTG | 9097 |
rs11447546 | in-del | -/C | 0.482406 | 0.0921269 | intron-variant | USP14 | GRCh38.p7 | 18:166012 | GCATTTAAAAAAAAA[-/C]ATTCTTGATTTTTAT | 9097 |
rs11558320 | snp | C/T | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:211839 | CCAGCCTATTGCAGG[C/T]TTTTCCTGACTTTAA | 9097 |
rs11663945 | snp | C/G | 0.196771 | 0.244268 | intron-variant | USP14 | GRCh38.p7 | 18:173269 | cctgccaccacaccc[C/G]gctattttttttgta | 9097 |
rs11665473 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157301 | tccctgtgacatgca[G/T]tgctgttcagcattt | 9097 |
rs11665479 | snp | C/G | 0 | 0 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157360 | tttctttcaaaatta[C/G]agtcaatcctgtcaa | 9097 |
rs11873070 | snp | C/G | 0.0524604 | 0.153226 | intron-variant | USP14 | GRCh38.p7 | 18:168076 | gattacaggcgccca[C/G]caccacgcccagcta | 9097 |
rs11873592 | snp | C/T | 0.0138799 | 0.0821421 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:156771 | aaagttatgtttcta[C/T]tatactgtagtctat | 9097 |
rs11875583 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | USP14 | GRCh38.p7 | 18:180486 | aatgctttttatagt[A/G]tttacaagtttgtgc | 9097 |
rs11876726 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | USP14 | GRCh38.p7 | 18:168110 | tttgtatttttagta[A/G]agatggggtttctcc | 9097 |
rs12051937 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:171027 | aaaaaaaaaaaaaaa[A/T]atatatatatatata | 9097 |
rs12052036 | snp | A/G | 0.144969 | 0.226867 | intron-variant | USP14 | GRCh38.p7 | 18:170950 | gtgcagcaaaccacc[A/G]tgacacaatgtttac | 9097 |
rs12454373 | snp | A/G | 0.0948562 | 0.196037 | intron-variant | USP14 | GRCh38.p7 | 18:196185 | aaaaattagccaggc[A/G]tggtggcatgctcct | 9097 |
rs12456191 | snp | A/G | 0.332106 | 0.236133 | intron-variant | USP14 | GRCh38.p7 | 18:178298 | CTAGGATTACAGCAT[A/G]AGCCACCATGCCTGG | 9097 |
rs12456452 | snp | C/T | 0.335101 | 0.23507 | intron-variant | USP14 | GRCh38.p7 | 18:168318 | tttgggcagattcca[C/T]tgggttttctgtgta | 9097 |
rs12953591 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:205137 | cacctaggcctccca[A/G]agtgctggggattat | 9097 |
rs12957104 | snp | A/G | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:205306 | TATACTTATCTCCTC[A/G]AAGTACTTCACGTAA | 9097 |
rs12960380 | snp | C/G | 0.0554779 | 0.157039 | intron-variant | USP14 | GRCh38.p7 | 18:191751 | actagatcagtaatt[C/G]TGAttgctccacaat | 9097 |
rs12960837 | snp | C/G | 0.251296 | 0.249997 | intron-variant | USP14 | GRCh38.p7 | 18:164285 | ATGTGGAACAATACA[C/G]ATAGGTTTGTTTTCT | 9097 |
rs12965796 | snp | G/T | 0.0707826 | 0.174302 | intron-variant | USP14 | GRCh38.p7 | 18:197292 | attggaacagcacac[G/T]tcccttcccctgatc | 9097 |
rs12967978 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:205261 | CTTAATATTTTCCTT[C/T]CCCCTGTAATCTGTA | 9097 |
rs12967981 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:205264 | AATATTTTCCTTCCC[C/T]CTGTAATCTGTAGCT | 9097 |
rs16944691 | snp | A/T | 0.196771 | 0.244268 | intron-variant | USP14 | GRCh38.p7 | 18:161240 | GCCTCTTTATGTATG[A/T]TTTAGGATGACTTAT | 9097 |
rs16945343 | snp | A/G | 0.197703 | 0.244469 | intron-variant | USP14 | GRCh38.p7 | 18:165453 | TTCATAGCCTAATCT[A/G]TGCTGAACACTGTAC | 9097 |
rs16948415 | snp | C/T | 0.213333 | 0.247296 | intron-variant | USP14 | GRCh38.p7 | 18:183621 | TTTTACTGATTCATA[C/T]GTCTACTTTGTTTCA | 9097 |
rs16951450 | snp | C/T | 0.210605 | 0.246877 | intron-variant | USP14 | GRCh38.p7 | 18:200576 | CCATACTAAAGAATA[C/T]GGACTCACATAAAAT | 9097 |
rs16952924 | snp | A/G | 0.211212 | 0.246973 | intron-variant | USP14 | GRCh38.p7 | 18:209527 | TTCATTTGTGCTGGC[A/G]TGGTAAGTGGACATG | 9097 |
rs16953056 | snp | A/G | 0.14665 | 0.227637 | intron-variant | USP14 | GRCh38.p7 | 18:210306 | CGTAATGTGAACTTT[A/G]GAGTTATTCTTGTTA | 9097 |
rs16953157 | snp | C/T | 0.00276638 | 0.0370883 | synonymous-codon | USP14 | GRCh38.p7 | 18:210453 | CCAGGGAAGGTCTAG[C/T]TCTTCAGGTCATTAT | 9097 |
rs17447476 | snp | C/G | 0.331179 | 0.236453 | intron-variant | USP14 | GRCh38.p7 | 18:182766 | CCAGCCTGGATGAGA[C/G]GTTAGGGAAGTGTGA | 9097 |
rs28412432 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | USP14 | GRCh38.p7 | 18:160754 | TCTTTAGCTTGTACT[A/G]TTGTAATATGCTTCT | 9097 |
rs28458892 | snp | A/G | 0.257454 | 0.249889 | intron-variant | USP14 | GRCh38.p7 | 18:189637 | ACAGGCGCGTGTCAC[A/G]ACGCCCAGCTAGTTT | 9097 |
rs28463286 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | USP14 | GRCh38.p7 | 18:185127 | TTAACAGTTACTAGG[C/T]TGCTGATTTTCTTTC | 9097 |
rs28555521 | snp | A/T | 0.337158 | 0.234315 | intron-variant | USP14 | GRCh38.p7 | 18:179766 | CAAATAAAAAAAAAA[A/T]TTTTTTTTTTTTTTT | 9097 |
rs28665633 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | USP14 | GRCh38.p7 | 18:160589 | ATTGCTTTGTTTTAA[A/T]CTTCAACGTAATCCT | 9097 |
rs28699057 | snp | G/T | 0.0368353 | 0.130617 | intron-variant | USP14 | GRCh38.p7 | 18:201021 | TTAGCCTGGATGGTC[G/T]CAATCTCCTGACCTT | 9097 |
rs33932265 | in-del | -/C | | | intron-variant | USP14 | GRCh38.p7 | 18:196927 | TAGTCTTAACTGATA[-/C]TCTGGCTTCTGCCTT | 9097 |
rs33952990 | in-del | -/C | | | intron-variant | USP14 | GRCh38.p7 | 18:166013 | CATTTAAAAAAAAAA[-/C]TTCTTGATTTTTATT | 9097 |
rs34029486 | in-del | -/G | | | intron-variant | USP14 | GRCh38.p7 | 18:186873 | AATTTGTGCTCATGT[-/G]CTTTGTTTTTATGCT | 9097 |
rs34094861 | in-del | -/TT | 0.237014 | 0.249662 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212170 | ATCCATTTAAAAATA[-/TT]TGTTATCTTCTTTGC | 9097 |
rs34124868 | in-del | -/G | | | intron-variant | USP14 | GRCh38.p7 | 18:208073 | TTTACTTTCAGGAGT[-/G]TTTATTTGTTTATTT | 9097 |
rs34207469 | in-del | -/TT | | | intron-variant | USP14 | GRCh38.p7 | 18:167954 | TTTTTTTTTTTTTTT[-/TT]GAGACAGAGTCTCAC | 9097 |
rs34265974 | in-del | -/T | 0.457154 | 0.139954 | intron-variant | USP14 | GRCh38.p7 | 18:174269 | TCACGTTTTTCTTTC[-/T]TTTTTTTTTTTTTTT | 9097 |
rs34411694 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | USP14 | GRCh38.p7 | 18:164130 | AACACTTTACAGTTA[C/T]CTGTATTGTGTGAAT | 9097 |
rs34496489 | snp | A/C | 0.279461 | 0.248258 | intron-variant | USP14 | GRCh38.p7 | 18:196993 | TCCTTTTTAAAATGA[A/C]GATAGGATTATGTTG | 9097 |
rs34628720 | in-del | -/G | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212768 | TGACTGATGCTAGGG[-/G]AAAGGATAAAGCATA | 9097 |
rs34807173 | in-del | -/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:185880 | TTTTTTTTTTTTTTT[-/T]AAGTAGAGACAAGAG | 9097 |
rs34845517 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:173059 | TTTTTTCTGTTTTCT[G/T]GTAAAGCTTGATAAG | 9097 |
rs34908804 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:185153 | TTTCATTTTTTTTTT[-/T]CTTATTTTTTATTTA | 9097 |
rs34983041 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:173100 | TACATTTAGATATAT[G/T]GTCTGTCTTTTTTTT | 9097 |
rs35100281 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:206344 | TTTATTTGCTATCTG[-/T]ATATCCTCTTTTGTA | 9097 |
rs35111217 | in-del | -/AT | 0.0034367 | 0.0413103 | intron-variant | USP14 | GRCh38.p7 | 18:196595 | TCGCGTGTATTAAAT[-/AT]GTGACTGTTTTACTA | 9097 |
rs35112033 | in-del | -/G | | | intron-variant | USP14 | GRCh38.p7 | 18:167708 | TTGTAGAGATGGGGG[-/G]TGTCACTATGTTGCC | 9097 |
rs35138898 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:208566 | TATCCTATGAATTTT[-/T]GATACATGGTATTTT | 9097 |
rs35140700 | in-del | -/TA | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213126 | AATGATTCATGTATA[-/TA]TTTGTATGATGCTTG | 9097 |
rs35327178 | in-del | -/A | | | intron-variant | USP14 | GRCh38.p7 | 18:204206 | AAATAAAAAAAAAAA[-/A]CCATAAGTTTATTCC | 9097 |
rs35399373 | in-del | -/C | 0.432944 | 0.170387 | intron-variant | USP14 | GRCh38.p7 | 18:196926 | GTAGTCTTAACTGAT[-/C]ATCTGGCTTCTGCCT | 9097 |
rs35489764 | in-del | -/T | 0.00252531 | 0.035444 | intron-variant | USP14 | GRCh38.p7 | 18:197742 | TTCGTTATACCTTGA[-/T]TTTTTTTTTTATTTT | 9097 |
rs35515450 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:162172 | GTTGCTCCCACTTTT[-/T]CGGCTGTTGTGAATA | 9097 |
rs35524629 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | USP14 | GRCh38.p7 | 18:198749 | TTTCTTATATGTCAA[A/G]GTGACTGTTAATAAT | 9097 |
rs35649176 | in-del | -/G | | | intron-variant | USP14 | GRCh38.p7 | 18:208908 | GTGCCACCATGCCTG[-/G]CTAATTTTTGTATTT | 9097 |
rs35705265 | snp | G/T | 0.444444 | 0.157135 | intron-variant | USP14 | GRCh38.p7 | 18:208602 | TCATTCTGTTCCTTG[G/T]ATTTTTAAAAATTTA | 9097 |
rs35802243 | in-del | -/G | | | intron-variant, frameshift-variant | USP14 | GRCh38.p7 | 18:178934 | TTTTTAAAAACAGGG[-/G]AATGACTCTACTAAT | 9097 |
rs35820003 | in-del | -/T | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212172 | CCATTTAAAAATATT[-/T]GTTATCTTCTTTGCC | 9097 |
rs35848582 | in-del | -/T | 0.291235 | 0.246576 | intron-variant | USP14 | GRCh38.p7 | 18:209122 | TTTTGATGTTTTGCC[-/T]TTTTTTTTTTGTCTT | 9097 |
rs35878431 | in-del | -/A | | | intron-variant | USP14 | GRCh38.p7 | 18:211010 | TGGGTCGCACTTGGA[-/A]GGACTGTTGGTGTGG | 9097 |
rs35897792 | snp | C/G | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:189520 | AAGGAGTCTCACTCT[C/G]CCTCCAGACTGGAGT | 9097 |
rs35941772 | in-del | -/A | | | intron-variant | USP14 | GRCh38.p7 | 18:200683 | TGGGGATATGTATAT[-/A]CTCTCGAAGGATCTC | 9097 |
rs35983571 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:189115 | GTATGGTTTTTTTTT[G/T]GTATTTTTATTTCTT | 9097 |
rs36038195 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:197761 | TTTTTTTATTTTTTT[-/T]CCCCTCAAAGGCTTA | 9097 |
rs36067290 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:189501 | CTTTGTTTTTTTTTT[-/T]GAGAAGGAGTCTCAC | 9097 |
rs36083125 | in-del | -/C | | | intron-variant | USP14 | GRCh38.p7 | 18:160263 | AGCCAAGATCGCGCC[-/C]ATTGCACTTCAGTCT | 9097 |
rs55916581 | snp | C/T | 0.373196 | 0.217538 | intron-variant | USP14 | GRCh38.p7 | 18:210698 | TAAGAAAGTTAGTTT[C/T]AAAAATGATAGTAAT | 9097 |
rs56225110 | snp | C/T | 0.331179 | 0.236453 | intron-variant | USP14 | GRCh38.p7 | 18:179642 | ACCCCGGCTGGAGTG[C/T]AGTGGTATGATCATA | 9097 |
rs56806027 | snp | A/T | 0.434398 | 0.168811 | intron-variant | USP14 | GRCh38.p7 | 18:204815 | CTTTGTATAGTATTA[A/T]TTGGATCAATCTGTA | 9097 |
rs57035428 | in-del | -/AAAA/AAAAA | | | intron-variant | USP14 | GRCh38.p7 | 18:204816 | TTGTATAGTATTATT[-/AAAA/AAAAA]TGGATCAATCTGTAT | 9097 |
rs57185071 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:198788 | AAATAAAAAAAGAAT[A/T]TTTTAATTTTATAAA | 9097 |
rs57735739 | snp | A/G | 0.195526 | 0.243993 | intron-variant | USP14 | GRCh38.p7 | 18:163736 | TACATATGCAGGTTT[A/G]TTATATAGGTAAACT | 9097 |
rs57888885 | in-del | -/TATATA | | | intron-variant | USP14 | GRCh38.p7 | 18:171056 | ATATATATATATATA[-/TATATA]AACTGAAGCTAGCAG | 9097 |
rs58838924 | in-del | -/AGA/TAGA | 0.249603 | 0.25 | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:213975 | ACAAGATAGATAGAT[-/AGA/TAGA]TAGATAGATAGATAG | 9097 |
rs59382008 | in-del | -/CAT | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213354 | ATTCCTTATCATCAT[-/CAT]TATAAAAAGCTTGAT | 9097 |
rs59541329 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:169493 | GTGTGATTTTTTTTT[-/T]CTTTTTTTCTGTTGG | 9097 |
rs59632306 | in-del | -/T | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:213970 | AATGGACAAGATAGA[-/T]TAGATTAGATAGATA | 9097 |
rs59833745 | in-del | -/A/AGAC/AGAT/AGATAGATAGAC | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214000 | GATAGATAGATAGAT[-/A/AGAC/AGAT/AGATAGATAGAC]GATGATTGATTGATG | 9097 |
rs60388591 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | USP14 | GRCh38.p7 | 18:209054 | AATGTGATTTAGGTA[C/T]AGACTATTTACATTT | 9097 |
rs60980138 | snp | A/G | 0.216349 | 0.247725 | intron-variant | USP14 | GRCh38.p7 | 18:168564 | CTCAACCTCCTGAGT[A/G]GTTGGGATTACAAAC | 9097 |
rs61110804 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP14 | GRCh38.p7 | 18:205402 | TGCATTATTGCCACA[A/G]GGCCACTTTTCTTCT | 9097 |
rs61560798 | snp | C/G/T | 0.625 | 0.125 | intron-variant | USP14 | GRCh38.p7 | 18:180863 | TTCATGGTTCATTCA[C/G/T]GTTACAGCACACGTA | 9097 |
rs61607000 | snp | A/G | 0.350327 | 0.228986 | intron-variant | USP14 | GRCh38.p7 | 18:204780 | TTTTTTTCCTGCTTC[A/G]TTTTTCCTTCAGAAC | 9097 |
rs61620947 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:164415 | TCATTTTTTTTTTTT[-/T]GGCCTTTATTGCATC | 9097 |
rs61644553 | snp | A/G | 0.256061 | 0.249927 | intron-variant | USP14 | GRCh38.p7 | 18:205096 | GCTGAGGCTAGTCTC[A/G]AACTCCTGAGCTCAG | 9097 |
rs61734347 | snp | A/G | 0.000462818 | 0.0152051 | missense | USP14 | GRCh38.p7 | 18:210398 | TAGATATTGGCTCCA[A/G]TAATTGTGGATACTA | 9097 |
rs62073488 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | USP14 | GRCh38.p7 | 18:169436 | AAAATTATGAAAGAC[C/T]GTTACATTTTGTTAA | 9097 |
rs62073489 | snp | A/G | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:170165 | GAAAAATAGCCGGGC[A/G]TAGTGGCACATGCCT | 9097 |
rs62073490 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | USP14 | GRCh38.p7 | 18:174203 | TTTCCTTTATTTAAA[C/T]GTTCAATGTTGGGAC | 9097 |
rs62073491 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | USP14 | GRCh38.p7 | 18:191652 | GAAACGTAAAATAAA[C/T]GGAATCCTACAGGTC | 9097 |
rs62073492 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:204206 | AAATAAAAAAAAAAA[A/C]CCATAAGTTTATTCC | 9097 |
rs62073493 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:204208 | ATAAAAAAAAAAAAC[A/C]ATAAGTTTATTCCAG | 9097 |
rs66730713 | in-del | -/CT | 0.0244538 | 0.107838 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212595 | GGTGACAGAGAGACT[-/CT]GTCTCAAAAAAAAAA | 9097 |
rs67330879 | in-del | -/GAT | 0.5 | 0 | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214021 | GATTGATTGATGATT[-/GAT]GATAGTAAATTATTT | 9097 |
rs68144137 | in-del | -/T/TTT | 0.256284 | 0.250656 | intron-variant | USP14 | GRCh38.p7 | 18:163818 | TACCCGATAGGTAGT[-/T/TTT]TTTTTTTTTTTTTTA | 9097 |
rs71174213 | in-del | -/AAATATATATATA | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:171024 | TAAAAAAAAAAAAAA[-/AAATATATATATA]TATATATATATATAT | 9097 |
rs71352926 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | USP14 | GRCh38.p7 | 18:175483 | CATTTTGTTAAATGC[C/T]TTTTCTATATCATTT | 9097 |
rs71352927 | snp | G/T | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:189145 | TATTTGTTATATTTG[G/T]GTTTTCCTCCCTTGA | 9097 |
rs71361486 | in-del | -/A/AACAA/AATAAA | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:204813 | ACTTTGTATAGTATT[-/A/AACAA/AATAAA]ATAAAAATGGATCAA | 9097 |
rs71689559 | in-del | -/TCTC | 0.333722 | 0.235565 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:211905 | ACATTTATTATTGTG[-/TCTC]TCTCTGATGTACTGT | 9097 |
rs71935241 | in-del | -/TG | 0.245061 | 0.249951 | intron-variant | USP14 | GRCh38.p7 | 18:180084 | TGGGGGAAATAAAAC[-/TG]TTTCTTTAGCGTGAA | 9097 |
rs72532176 | in-del | -/GTA | | | intron-variant | USP14 | GRCh38.p7 | 18:195383 | GTGCTAAGATGCWGT[-/GTA]AKTTGGTGGGTTCAG | 9097 |
rs72856233 | snp | A/G | 0.333722 | 0.235565 | intron-variant | USP14 | GRCh38.p7 | 18:174088 | CTTGTCATTTTCTCC[A/G]TAAGAGTCTGCTGGG | 9097 |
rs72856234 | snp | A/G | 0.332337 | 0.236052 | intron-variant | USP14 | GRCh38.p7 | 18:174996 | GGCCAGGCTGTTCTC[A/G]AACTGGTCTCAAGCA | 9097 |
rs72856237 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | USP14 | GRCh38.p7 | 18:185252 | GCAGCCTCTGCCTCC[C/T]GGCTTGAGCAATTCT | 9097 |
rs72856238 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | USP14 | GRCh38.p7 | 18:186471 | TTAAAAAAAGAGATG[G/T]GCCAGGAGCAGTGGC | 9097 |
rs72856240 | snp | G/T | 0.349452 | 0.229367 | intron-variant | USP14 | GRCh38.p7 | 18:192228 | TGTTATTTTATTTTC[G/T]TTGTAATTAATGAAT | 9097 |
rs72856250 | snp | C/T | 0.350546 | 0.22889 | intron-variant | USP14 | GRCh38.p7 | 18:205757 | CAGCACTCCAACCTG[C/T]ATAACAAAGCAAGAC | 9097 |
rs72856253 | snp | C/T | 0.33533 | 0.234987 | intron-variant | USP14 | GRCh38.p7 | 18:208512 | CCTTTATTCTGCTTG[C/T]CTTGTGATATAAATT | 9097 |
rs73362400 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | USP14 | GRCh38.p7 | 18:166237 | TTTAGTATTTGATGC[C/T]GTAAATACAGGTTAC | 9097 |
rs73364303 | snp | A/G | 0.253264 | 0.249979 | intron-variant | USP14 | GRCh38.p7 | 18:168247 | CAGTTGATTTTTCTA[A/G]GTTTATTTTCATTCT | 9097 |
rs73364326 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | USP14 | GRCh38.p7 | 18:176523 | TTTTAAGCCTTTTTT[A/T]AAATCTCTTTTGCTC | 9097 |
rs73364329 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | USP14 | GRCh38.p7 | 18:177027 | TAAATTTATATAACT[A/C]TAATTGCATCTTTAT | 9097 |
rs73364334 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | USP14 | GRCh38.p7 | 18:182976 | AGAGAAACCATTGGA[A/G]GATTTTAAGCAGAGT | 9097 |
rs73364336 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | USP14 | GRCh38.p7 | 18:185521 | CATATTATGAGAGGC[A/C]TGCAAGAACTGAGAC | 9097 |
rs74257617 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP14 | GRCh38.p7 | 18:164834 | TTAAAAAGAGAAGAA[A/G]CCTAATTTTTGTCTT | 9097 |
rs74361874 | snp | G/T | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:179249 | CTAGGGGTTTTTTTT[G/T]GTATTGTACACCTTA | 9097 |
rs74479856 | snp | G/T | 0.0145014 | 0.083907 | synonymous-codon | USP14 | GRCh38.p7 | 18:211194 | AGAAGATATCTTACG[G/T]CTTTCTGGTGGTGGA | 9097 |
rs74705064 | snp | A/G | 0.212425 | 0.24716 | intron-variant | USP14 | GRCh38.p7 | 18:158795 | CCTGCACGGGCGGGC[A/G]CCCGGCATGGACTGG | 9097 |
rs74816514 | snp | C/T | 0.000271186 | 0.0116413 | intron-variant | USP14 | GRCh38.p7 | 18:197729 | GTGATTATAGACTTT[C/T]GTTATACCTTGATTT | 9097 |
rs74850634 | snp | A/G | 0.210301 | 0.246828 | intron-variant | USP14 | GRCh38.p7 | 18:202197 | TTAAATGTAGAGTAT[A/G]TGCCAAATATTTTAC | 9097 |
rs75515343 | snp | C/T | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:174270 | CACGTTTTTCTTTCT[C/T]TTTTTTTTTTTTTTT | 9097 |
rs75525833 | snp | C/G | 0.146985 | 0.227789 | intron-variant | USP14 | GRCh38.p7 | 18:206700 | AGGTCAGGGGTTCGA[C/G]ACCAGCCTGGCAAAC | 9097 |
rs75659953 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | USP14 | GRCh38.p7 | 18:199945 | CTAACAAAATCAACT[A/G]TATAGTCAGAAATCA | 9097 |
rs75750888 | snp | C/T | 0.000394011 | 0.0140303 | missense | USP14 | GRCh38.p7 | 18:204576 | TAGGATGTTAAATTT[C/T]CTCTTATGTTGGATA | 9097 |
rs75764515 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | USP14 | GRCh38.p7 | 18:180584 | AGTCACTCCTTTAAC[A/C]CCTTCACCCACCTCT | 9097 |
rs75765161 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157950 | ATATAAATATATAAA[A/T]ATATATAAATATATA | 9097 |
rs75894241 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157559 | GAGATTGCAGCAATT[C/T]AGTCACATCTGTGGG | 9097 |
rs75964793 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214219 | CTCTGCTTGAAAGCA[C/T]GAATAAGTGAGAACA | 9097 |
rs76288486 | snp | C/T | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:180212 | TTAATGATTTAATCC[C/T]TTTTTTTTTTTTTTT | 9097 |
rs76347333 | snp | A/C | 0.34944 | 0.229372 | intron-variant | USP14 | GRCh38.p7 | 18:166012 | TGCATTTAAAAAAAA[A/C]ATTCTTGATTTTTAT | 9097 |
rs76487886 | snp | A/T | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:204195 | AGTTGTATTTCAAAT[A/T]AAAAAAAAAAACCAT | 9097 |
rs76518738 | snp | C/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:195046 | AAAGTTTTTTTTTTT[C/T]CCTTCTTCAGGATTC | 9097 |
rs76588552 | snp | A/T | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:197469 | TTCTAGAATGCTTTA[A/T]TTTTTGGAAGATCGT | 9097 |
rs76709408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:188291 | TACATGTTAAAATTA[C/T]CAAATGTTGTTTGTT | 9097 |
rs76777390 | snp | C/T | 0.202343 | 0.245416 | intron-variant | USP14 | GRCh38.p7 | 18:199067 | TATGTTGAAATGAAT[C/T]TTGGGAGACTAAAAG | 9097 |
rs76782740 | snp | C/T | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:188508 | CTGTCTCCCTCTGGC[C/T]TTTTTTTTTTTTTTT | 9097 |
rs76818616 | in-del | -/AA | | | frameshift-variant | USP14 | GRCh38.p7 | 18:202913 | CCAAACAGTCTCCAA[-/AA]CGTTGCAAAGAAATG | 9097 |
rs76836289 | snp | A/C | 0.5 | 0 | intron-variant, missense | USP14 | GRCh38.p7 | 18:178948 | GGAATGACTCTACTA[A/C]TGATGGGGTCAGCAG | 9097 |
rs76860101 | snp | C/T | 0.147321 | 0.227941 | intron-variant | USP14 | GRCh38.p7 | 18:188826 | GGGATTACAGGCACC[C/T]GCCACTATGCCCAGC | 9097 |
rs76927248 | snp | G/T | 0.142609 | 0.225759 | intron-variant | USP14 | GRCh38.p7 | 18:164964 | TATTATTATTTTTTT[G/T]GGGATTGAGTCTCCC | 9097 |
rs77098792 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:204816 | TTTGTATAGTATTAT[A/T]TGGATCAATCTGTAT | 9097 |
rs77153925 | in-del | -/T | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:213975 | ACAAGATAGATAGAT[-/T]AGATAGATAGATAGA | 9097 |
rs77205434 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | USP14 | GRCh38.p7 | 18:161221 | GCATGAGCCACCATT[C/T]CCGGCCTCTTTATGT | 9097 |
rs77306113 | snp | C/G | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:160281 | TGCACTTCAGTCTGG[C/G]TGAAAAAAGCGAAAC | 9097 |
rs77363148 | snp | A/G | 0.202651 | 0.245475 | intron-variant | USP14 | GRCh38.p7 | 18:188843 | CCACTATGCCCAGCT[A/G]ATTTTTTGTATTTTT | 9097 |
rs77381524 | snp | C/T | 0.202343 | 0.245416 | intron-variant | USP14 | GRCh38.p7 | 18:168724 | ACAGGCGTGAGCCAC[C/T]GTGCCAGGCCTTGTC | 9097 |
rs77382114 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | USP14 | GRCh38.p7 | 18:187327 | TGTTTGTATTATGCC[A/G]TTTTAACCATCTGGT | 9097 |
rs77511266 | snp | A/G | 0.0230013 | 0.104745 | intron-variant | USP14 | GRCh38.p7 | 18:178879 | TTCTTTTGGTTTGAC[A/G]TAAACATTACCAACT | 9097 |
rs77935765 | snp | C/T | 0.207253 | 0.246318 | intron-variant | USP14 | GRCh38.p7 | 18:192543 | GCACTCCAACCTGGG[C/T]GACAAGAGCAAAACT | 9097 |
rs77944907 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:167953 | TTTTTTTTTTTTTTT[C/T]TGAGACAGAGTCTCA | 9097 |
rs78209482 | snp | C/T | 0.14665 | 0.227637 | intron-variant | USP14 | GRCh38.p7 | 18:209241 | TGTAGGTGATTTCAT[C/T]ATCTGTATAAAAAAG | 9097 |
rs78491468 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | USP14 | GRCh38.p7 | 18:181870 | CTTTTAGCTCTTCTA[C/T]TCAGGCCTGTGGTTA | 9097 |
rs78624044 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | USP14 | GRCh38.p7 | 18:185503 | TCAGTTCAGTGAGAT[G/T]CTCATATTATGAGAG | 9097 |
rs78690444 | snp | A/C | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:186752 | GGGAGACTGTGTCTC[A/C]AAAAAAAAAGAGAAA | 9097 |
rs78819268 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:203538 | GTCCTCAGCTTCAGG[G/T]ATACTGATTCAGTAG | 9097 |
rs78839044 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | USP14 | GRCh38.p7 | 18:203318 | TAGGGGAGCTAATAT[G/T]AGACAAGTGATTCTT | 9097 |
rs78955421 | snp | G/T | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:204918 | CCTTTTTTTTTTTTT[G/T]TGACAAGGTCTTCCT | 9097 |
rs79002808 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | USP14 | GRCh38.p7 | 18:179536 | ATTTTTTTTTTAACA[C/G]CTAGCATTTATTTAG | 9097 |
rs79017281 | snp | G/T | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:204917 | TCCTTTTTTTTTTTT[G/T]GTGACAAGGTCTTCC | 9097 |
rs79166095 | snp | C/T | 0.144296 | 0.226554 | intron-variant | USP14 | GRCh38.p7 | 18:172204 | GATTGTGCCACTGCA[C/T]TCCAATCTGAGTGAC | 9097 |
rs79416573 | snp | A/C | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:186751 | AGGGAGACTGTGTCT[A/C]AAAAAAAAAAGAGAA | 9097 |
rs79739376 | snp | A/C | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:196523 | ACCAAGACTCCATCT[A/C]AAAAAAAAAAAAAAT | 9097 |
rs79751736 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | USP14 | GRCh38.p7 | 18:167426 | GAGTATTAAAATCCC[C/T]GAATATGATGTACTT | 9097 |
rs79829832 | in-del | -/T | 0.367309 | 0.220768 | intron-variant | USP14 | GRCh38.p7 | 18:180212 | TTAATGATTTAATCC[-/T]TTTTTTTTTTTTTTT | 9097 |
rs80278531 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:197753 | TTGATTTTTTTTTTT[A/T]TTTTTTTTCCCCTCA | 9097 |
rs111248914 | snp | A/C | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:175901 | TAGGAAGACTTTAAG[A/C]ATTTAGTGTCTTTAA | 9097 |
rs111250834 | snp | C/T | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:164700 | CTCAAGTGATCTGCC[C/T]ACCTTGGCCTCCCAG | 9097 |
rs111302645 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:181025 | CCTCATTCCTATTTT[A/C]TGGCTGAATAGTATT | 9097 |
rs111311471 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP14 | GRCh38.p7 | 18:202667 | GGAATCCACAACAAC[A/G]TAAATTATTTGATGC | 9097 |
rs111402610 | in-del | -/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:203378 | CTATTGTCTTTTTTA[-/T]TTTTTAACTGTACAC | 9097 |
rs111543418 | snp | A/G | | | missense | USP14 | GRCh38.p7 | 18:196732 | GCTTTCCCACAGTTT[A/G]CCGAGAAAGGTGAAC | 9097 |
rs111667866 | snp | A/G | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:190649 | TCATAGGGACTAGAA[A/G]AGTCAAAATGTCCTC | 9097 |
rs111695061 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP14 | GRCh38.p7 | 18:175051 | GTGCTGGGATTACAA[A/G]CGTGAGCCACTGCAC | 9097 |
rs111700513 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:171036 | AAAAAATATATATAT[A/C]TATATATATATATAT | 9097 |
rs111712007 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP14 | GRCh38.p7 | 18:186809 | GTTTTTTCTTTAAAC[A/G]TATGTGTAGCAGTGT | 9097 |
rs111713539 | snp | C/T | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:163166 | TGCATGCATGCTCCT[C/T]TTGATTAGGTAAGTG | 9097 |
rs111721288 | snp | A/G | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:180956 | TAACACCTCATTCCT[A/G]TTTTATGGCTGAATA | 9097 |
rs111728247 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | USP14 | GRCh38.p7 | 18:173138 | CTTTGAGACGGAGTC[G/T]CACCCTGTTGCCCAG | 9097 |
rs111778916 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | USP14 | GRCh38.p7 | 18:174525 | CCTGCCTTGGCCTCC[C/T]CAAGTGCTGGGATTA | 9097 |
rs111846918 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | USP14 | GRCh38.p7 | 18:169718 | CACCTTGCATCGAGC[A/G]AGTTTATAGGCACCA | 9097 |
rs111881258 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:174974 | AGAGATGGGGTTTTG[C/T]CATGTTGGCCAGGCT | 9097 |
rs111884175 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | USP14 | GRCh38.p7 | 18:168011 | GGCGCGATCTCGGCT[C/T]GCTGCAACCTCTGCC | 9097 |
rs111894809 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:204814 | ACTTTGTATAGTATT[A/T]TTTGGATCAATCTGT | 9097 |
rs111903285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:197512 | GCTTAATATTTTTAA[A/G]GAAGGAAACCACTTT | 9097 |
rs111939515 | snp | C/T | 0 | 0 | upstream-variant-2KB, downstream-variant-500B | USP14, LOC105371951 | GRCh38.p7 | 18:158291 | TGCCGCAGGGCTGGG[C/T]CGCGCCAGGACCACG | 9097 |
rs112097871 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157528 | AGCGACTCCTTGCCC[A/G]TTAAAGCTTTGTCTT | 9097 |
rs112178323 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP14 | GRCh38.p7 | 18:186492 | GAGCAGTGGCTCATG[C/G]TTGTAATCCCAGCAC | 9097 |
rs112206684 | snp | A/G | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:164179 | GTATTAAAAGTATTA[A/G]TTTTATTTTGTTTAG | 9097 |
rs112220713 | snp | A/G | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:181020 | TAACACCTCATTCCT[A/G]TTTTATGGCTGAATA | 9097 |
rs112317506 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | USP14 | GRCh38.p7 | 18:160479 | TGTGATCTGTGATCA[C/T]GCCACTGCACTCCAG | 9097 |
rs112362155 | snp | C/T | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:180795 | GTATTTCATGGTTCA[C/T]TCACGTTACAGCACA | 9097 |
rs112401149 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:158916 | AGGGGAGCGCCGTCC[C/T]CCTGAGCCACCGATG | 9097 |
rs112449441 | snp | G/T | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:180355 | GTAAGACTGCAGTCT[G/T]TTTTGGGTAAGGGAT | 9097 |
rs112482020 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | USP14 | GRCh38.p7 | 18:191140 | TTAGTACTTAATTTT[A/G]ATTTCAAAAATGCCT | 9097 |
rs112546151 | snp | A/G | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:163724 | TAGGTTCTGAGATAC[A/G]TATGCAGGTTTGTTA | 9097 |
rs112640574 | in-del | -/T | 0.499913 | 0.00658888 | intron-variant | USP14 | GRCh38.p7 | 18:174610 | TGGTACTTTTCTTTC[-/T]TTTTTTTTTTTTTTT | 9097 |
rs112707229 | snp | A/G | 0.0295035 | 0.117819 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:156976 | GAGGCTGAGGTGAGA[A/G]GATAGCTTGAGCTGG | 9097 |
rs112736425 | snp | A/G | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:199041 | TTGGTAGCCAAATGA[A/G]CATTCTTAAGTATGT | 9097 |
rs112760914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:159373 | TCATTTCTTGATTGG[C/T]GTTTGACAGGGGCTT | 9097 |
rs112775395 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:200820 | TTATTTACTTATTTT[C/G]AGACGGAGTCTCTCT | 9097 |
rs112840039 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, downstream-variant-500B | USP14, LOC105371951 | GRCh38.p7 | 18:158276 | AGTTCCCACTTCATC[C/T]GCCGCAGGGCTGGGC | 9097 |
rs112941471 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | USP14 | GRCh38.p7 | 18:173321 | TTTCACCATGTTAGC[C/T]AGGATGGTCTCTATC | 9097 |
rs112954076 | snp | A/G | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:181084 | TAACACCTCATTCCT[A/G]TTTTATGGCTGAATA | 9097 |
rs112989409 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP14 | GRCh38.p7 | 18:174649 | AGGTCTTGCTTTGTC[A/G]GCTGGAGTGCAGTGG | 9097 |
rs113002946 | in-del | -/TAAAA | 0.262159 | 0.249704 | intron-variant | USP14 | GRCh38.p7 | 18:166711 | TGTTTTGAAGTACAT[-/TAAAA]TAAATTGATTATTAG | 9097 |
rs113020722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:202328 | TTTCCACTGTTACAC[A/G]GGCTGTAAGAAGCAG | 9097 |
rs113023311 | snp | A/G | 0.345037 | 0.231231 | intron-variant | USP14 | GRCh38.p7 | 18:166392 | GGCTGGAGTGCAGTG[A/G]TGAGATCTCGGCTCA | 9097 |
rs113128272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:174633 | TTTTTTTTTAAAGAC[A/G]AGGTCTTGCTTTGTC | 9097 |
rs113148782 | snp | C/G | 0.5 | 0 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:211949 | TTTAACTTTGGAATG[C/G]CTTTGTAATAATCAG | 9097 |
rs113258475 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:196336 | AGCCTGGCCAGCATG[G/T]TGAAACCCCATCTCT | 9097 |
rs113367384 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP14 | GRCh38.p7 | 18:180799 | TTCATGGTTCACTCA[C/T]GTTACAGCACACGTA | 9097 |
rs113443950 | snp | A/G | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:180828 | TAACACCTCATTCCT[A/G]TTTTATGGCTGAATA | 9097 |
rs113476752 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP14 | GRCh38.p7 | 18:159311 | TTCTGTATCCGAAAC[C/G]TGGTGTGAGCTTTCA | 9097 |
rs113588904 | in-del | -/TGA | 0.0166325 | 0.0896639 | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214017 | TGATTGATTGATGAT[-/TGA]TGATAGTAAATTATT | 9097 |
rs113666360 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP14 | GRCh38.p7 | 18:172526 | GCTATTAAACAGCAC[C/T]GCAAGCTACAGAGAA | 9097 |
rs113718574 | snp | C/T | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:180714 | ACTTCTTTCATTTGG[C/T]ATGTTCCCATGGTTC | 9097 |
rs113753392 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP14 | GRCh38.p7 | 18:174632 | TTTTTTTTTTAAAGA[C/T]GAGGTCTTGCTTTGT | 9097 |
rs113753917 | snp | A/G | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:210333 | GTTACTTAGCTTGAG[A/G]AGGCACATGTCTATT | 9097 |
rs113760297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:194151 | AGTGTTATCTCATTG[C/T]TGTCAACCATTGATT | 9097 |
rs113800937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:180764 | TAACACCTCATTCCT[A/G]TTTTATGGCTGAATA | 9097 |
rs113886010 | in-del | -/A | 0.5 | 0 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213519 | GGAGAGGAGTAGGCC[-/A]AAAAAAAAAAAGTCT | 9097 |
rs113915721 | snp | A/G | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:180892 | TAACACCTCATTCCT[A/G]TTTTATGGCTGAATA | 9097 |
rs113920726 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP14 | GRCh38.p7 | 18:181975 | CATTTGTTGAAGGCT[A/G]TTGTTTCCCCACTGA | 9097 |
rs113991831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:191917 | AATGATAATTTCTGA[A/G]CTTTTGTAATAAGAC | 9097 |
rs113995585 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | USP14 | GRCh38.p7 | 18:169252 | AAAAATTAGCCGAGT[A/G]TCATGGTGCACGCCA | 9097 |
rs114034581 | snp | C/T | 0.040671 | 0.13668 | intron-variant | USP14 | GRCh38.p7 | 18:161371 | CTTTATGCTGTGGAA[C/T]GTTTTCCTTCTTTTC | 9097 |
rs114124773 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | USP14 | GRCh38.p7 | 18:162092 | CCTTTTTAAGGTTGA[A/G]TAATATTCCGTTGTA | 9097 |
rs114191677 | snp | C/T | 0.0123036 | 0.0774623 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157358 | AATTTCTTTCAAAAT[C/T]AGAGTCAATCCTGTC | 9097 |
rs114268776 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:206257 | TTTCAGCCATTGGAT[A/T]GGTTTATAGTGATAC | 9097 |
rs114319796 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | USP14 | GRCh38.p7 | 18:191951 | GTGTGAGTAATGACT[A/G]TGGTTTGAATAGTCA | 9097 |
rs114384348 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:178559 | CCACTACCACAATCA[C/G]GATTTAGAAGTTTCA | 9097 |
rs114442885 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | USP14 | GRCh38.p7 | 18:176947 | GAAATTTCTTAGCTA[C/T]TATCCTGGGTATAAA | 9097 |
rs114575888 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP14 | GRCh38.p7 | 18:184283 | AGTGCACTTACTAAC[A/G]TAATTGATACAAGAT | 9097 |
rs114826110 | snp | C/T | 0.0360663 | 0.129354 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157765 | ATAGTAATCATAGAT[C/T]ACTGGAACAGATATA | 9097 |
rs115280969 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | USP14 | GRCh38.p7 | 18:178128 | CAGGCTCCAGTGATC[C/T]TCCCATTTTAGCCCC | 9097 |
rs115281583 | snp | A/T | 0.0322114 | 0.122752 | intron-variant | USP14 | GRCh38.p7 | 18:191927 | TCTGAGCTTTTGTAA[A/T]AAGACATTGTGTGAG | 9097 |
rs115299702 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | USP14 | GRCh38.p7 | 18:189106 | ATTGGACCTGTATGG[G/T]TTTTTTTTTGTATTT | 9097 |
rs115445128 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | USP14 | GRCh38.p7 | 18:159850 | AATATTTAATCAGAT[A/C]TTTTCCTCATCCCCC | 9097 |
rs115488861 | snp | C/T | 0.0138799 | 0.0821421 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:158011 | TATATATATATAGAA[C/T]GCAATAAAATGAGGT | 9097 |
rs115546629 | snp | A/C | 0.0333238 | 0.124705 | intron-variant | USP14 | GRCh38.p7 | 18:183956 | GCTGATGGAGATAGC[A/C]TTGGCTCACTTCCAA | 9097 |
rs115627554 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | USP14 | GRCh38.p7 | 18:207573 | AGTCCCAGCTGTTCA[A/G]AAGGCTAAGGTGGGA | 9097 |
rs115676441 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | USP14 | GRCh38.p7 | 18:186854 | AACCAATTCAAACAG[C/T]CTTAAATTTGTGCTC | 9097 |
rs115694628 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | USP14 | GRCh38.p7 | 18:167329 | TTCTTATGCTCTCCA[A/G]CTTTCTCCTCTTTGA | 9097 |
rs115784782 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP14 | GRCh38.p7 | 18:210808 | GGCTTAAATAGGAGG[C/T]AGCTGGGTTCTCCTG | 9097 |
rs115792860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:172514 | TGTGGATAAAATGCT[A/G]TTAAACAGCACCGCA | 9097 |
rs115853102 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | USP14 | GRCh38.p7 | 18:169956 | TTCCCTCCTCCCTCT[C/T]CTCGAGCCTCCCTAT | 9097 |
rs115907518 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | USP14 | GRCh38.p7 | 18:190653 | AGGGACTAGAAAAGT[C/T]AAAATGTCCTCTCTT | 9097 |
rs115911406 | snp | C/T | 0.0244435 | 0.107816 | intron-variant | USP14 | GRCh38.p7 | 18:204518 | TACTTTAAATAAATA[C/T]CTTTATAAATGTGTT | 9097 |
rs116019523 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | USP14 | GRCh38.p7 | 18:176083 | CGTTTTCCTCTCTAG[C/T]ATTGGCAAATTATGA | 9097 |
rs116066120 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:181612 | TTTTCTTCTATACTA[C/T]AAGCTGTCATTTTAC | 9097 |
rs116082797 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP14 | GRCh38.p7 | 18:159506 | ATATGTGTGGTGTCT[C/T]CAATTGGCTGTAGGT | 9097 |
rs116157283 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP14 | GRCh38.p7 | 18:198509 | CAGGTGTGAGCCACC[A/G]CGCCCAGCCCAGAGG | 9097 |
rs116387496 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | USP14 | GRCh38.p7 | 18:206315 | GCTGATGAAGTTGAG[C/T]ATGTCTTCATGTGTT | 9097 |
rs116443871 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | USP14 | GRCh38.p7 | 18:190651 | ATAGGGACTAGAAAA[A/G]TCAAAATGTCCTCTC | 9097 |
rs116502592 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:175993 | TTAAGGAATTGGTTC[A/G]TTTAAGTTGCTGAAT | 9097 |
rs116503853 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:165961 | GAGGGGAAAGGCCTA[A/G]CTGTAGTTAGTAAAA | 9097 |
rs116616328 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | USP14 | GRCh38.p7 | 18:206200 | AGACTGATTCACTTT[C/T]TCTGCATTCTCACCA | 9097 |
rs116757817 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | USP14 | GRCh38.p7 | 18:183463 | TCATTATTTCTTTAG[A/G]TACTGCTTCTCCTCC | 9097 |
rs116939866 | snp | C/T | 0.00874735 | 0.0655527 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213466 | TAACTAATAAGGCTA[C/T]TTTAGAATTCAGCCT | 9097 |
rs117004609 | snp | G/T | 0.0244538 | 0.107838 | intron-variant | USP14 | GRCh38.p7 | 18:170848 | AACAGCACACACGGG[G/T]GCCTGTCAGGCAGTG | 9097 |
rs117052953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:161909 | TTTTAATGATTTTTA[C/T]GTATACAGTTCTATA | 9097 |
rs117349903 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:160791 | TTTTAGTGATTACAG[A/T]ATGCCTTCTTCAAGC | 9097 |
rs117405005 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | USP14 | GRCh38.p7 | 18:178216 | GTAGAGATGGGATTT[C/T]GCCATGTTGCCCAGG | 9097 |
rs117533958 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | USP14 | GRCh38.p7 | 18:178747 | GAAAGAAACTTGTAC[A/C]ATTTAAGGTCACTCC | 9097 |
rs117584140 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP14 | GRCh38.p7 | 18:159290 | TCATCAAACGTTGCA[C/T]TGGATTTCTGTATCC | 9097 |
rs117638889 | snp | C/T | 0.0146672 | 0.084371 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:156619 | ATCTTATTTAGTCCT[C/T]ATAACAATCCTGAGA | 9097 |
rs117642806 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP14 | GRCh38.p7 | 18:204320 | TCTGTGGTTAGTTTT[A/G]TGGGTTAGAGTATTT | 9097 |
rs117692694 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | USP14 | GRCh38.p7 | 18:171227 | TACAACAGATTTTCA[A/G]TGTGGATGAAGCAGC | 9097 |
rs118018519 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | USP14 | GRCh38.p7 | 18:191386 | GATTTCTTTCATACT[A/G]CTTAACATAAGCATA | 9097 |
rs118177450 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | USP14 | GRCh38.p7 | 18:175846 | ATTCTCTAGTGAAGC[C/G]TAGTTCACTAGACTT | 9097 |
rs118184408 | snp | A/C | 0.0267878 | 0.112589 | intron-variant | USP14 | GRCh38.p7 | 18:186226 | CAGTGCTTTGGGAGG[A/C]TGAATCTATAGCTTG | 9097 |
rs137907259 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP14 | GRCh38.p7 | 18:165034 | GCTAACTGCAACCAC[C/T]GCCTCCCGGGCTCAA | 9097 |
rs138069283 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | USP14 | GRCh38.p7 | 18:194498 | TTACTAACTTTTAGT[C/T]GCATTTGGTTTCTCA | 9097 |
rs138104273 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:179552 | CTAGCATTTATTTAG[C/T]GCCATTCATTCATTT | 9097 |
rs138126708 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:211844 | CTATTGCAGGCTTTT[C/T]CTGACTTTAAAATAA | 9097 |
rs138148987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:208314 | GTATTTATTACCCTT[C/T]TGATGTCTGTAGAGT | 9097 |
rs138275331 | snp | C/G | 0.0118686 | 0.0761147 | synonymous-codon | USP14 | GRCh38.p7 | 18:204602 | GGATATGTATGAACT[C/G]TGTACACCAGAACTT | 9097 |
rs138293685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:178331 | TGAATTTTATTAGTT[A/G]TAAGTTTGTTATGGA | 9097 |
rs138425645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:165549 | ACCATTTATTGAGTA[C/T]TTATTTTATGTCAGG | 9097 |
rs138427514 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:191780 | ATCTTGCCGATATTG[C/G]GTGATACTAGTTTTT | 9097 |
rs138458391 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:169673 | TGCTTCACAGATAAT[C/T]GTGATTTTTATAAGT | 9097 |
rs138481413 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | USP14 | GRCh38.p7 | 18:161130 | ACGAGGTTTCACCGT[A/C]TTGGCCAGGCTGGTC | 9097 |
rs138492288 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:172628 | TTCAGGAACCAGTGC[C/G/T]GTGATCAGTCAGTAG | 9097 |
rs138620900 | in-del | -/A | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213530 | GCCAAAAAAAAAAAA[-/A]GTCTTGATTCCTGAA | 9097 |
rs138622253 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP14 | GRCh38.p7 | 18:159956 | TCAGCAAAAAGCTCT[A/G]TATTAAAATGAAGAG | 9097 |
rs138654675 | snp | G/T | 0.00019015 | 0.00974879 | intron-variant | USP14 | GRCh38.p7 | 18:197740 | CTTTCGTTATACCTT[G/T]ATTTTTTTTTTTATT | 9097 |
rs138744404 | snp | A/T | 0.0221141 | 0.102801 | intron-variant | USP14 | GRCh38.p7 | 18:185013 | TGTTATAAAAAAATC[A/T]TCCTAAAATTCTATA | 9097 |
rs138796746 | snp | A/G | 0.0016636 | 0.028793 | synonymous-codon | USP14 | GRCh38.p7 | 18:163396 | GGCTCAGCTGTTTGC[A/G]TTGACTGGAGTCCAG | 9097 |
rs138816156 | snp | A/G | 3.33061e-05 | 0.00408068 | missense | USP14 | GRCh38.p7 | 18:211274 | TAATGGAAGAGGAAA[A/G]TGAACAGTAATCTTC | 9097 |
rs138830841 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:175139 | AAGTTAATTTTTATA[A/G]TTGACTTTGTATCCT | 9097 |
rs138890184 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:169393 | AAAAAGAGTGGACAT[C/G]TTGTCTTATTCTAGT | 9097 |
rs139001387 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | USP14 | GRCh38.p7 | 18:205114 | CTCCTGAGCTCAGGC[A/G]ATCTGCCCACCTAGG | 9097 |
rs139044741 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:173533 | TCTCCTGCCTCAGCC[G/T]CCTGAGTAGCTGGGA | 9097 |
rs139115406 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP14 | GRCh38.p7 | 18:186147 | TGAAAATGCATCATA[C/T]ATTTAATTCATACAG | 9097 |
rs139153645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:170367 | AAGTGTTCAAGAGAA[A/G]GGAAGAGTTTCATGT | 9097 |
rs139244031 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | USP14 | GRCh38.p7 | 18:196124 | TCAGGAGTTCGAGAC[C/T]AGCCTGGCCAACATG | 9097 |
rs139399909 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | USP14 | GRCh38.p7 | 18:196392 | AGCCGGGAATGGTGG[C/T]GTGTGCCTGTAATCC | 9097 |
rs139411544 | snp | A/G/T | 6.61408e-05 | 0.00575031 | missense | USP14 | GRCh38.p7 | 18:204630 | CTTCAAGAGAAAATG[A/G/T]TGTCTTTTCGATCCA | 9097 |
rs139435118 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:181823 | TAGGTTACAAAGACT[G/T]ACTTCTTTGTTGTTT | 9097 |
rs139471110 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | USP14 | GRCh38.p7 | 18:209474 | ATTTAAATCATACCT[A/C]TTTAATGTAGGTAAG | 9097 |
rs139518441 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | USP14 | GRCh38.p7 | 18:167290 | CGTCTCCAAAAAAAG[A/T]GTCTTGAAATAAGAT | 9097 |
rs139573097 | snp | A/T | 0.021333 | 0.101051 | intron-variant | USP14 | GRCh38.p7 | 18:205462 | TACCAACCCGTTCAT[A/T]TCTATAATTTTTGTC | 9097 |
rs139597169 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | USP14 | GRCh38.p7 | 18:201049 | CTTGTGATCCGCCCA[C/T]CTCGGCCTCCCAAAG | 9097 |
rs139646538 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:205357 | TTGATGCAGTCAAAA[C/T]ACAGTACATTTCCAT | 9097 |
rs139646626 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP14 | GRCh38.p7 | 18:163145 | GAAATTTTATTCAGC[A/G]CCTACTGCATGCATG | 9097 |
rs139745469 | snp | C/G/T | 0.00636936 | 0.0560724 | intron-variant | USP14 | GRCh38.p7 | 18:167553 | CACTCTCACGTATGC[C/G/T]GGAGCACAGTGGCAT | 9097 |
rs139753931 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | USP14 | GRCh38.p7 | 18:205862 | ATAATTCTCTGGCGA[C/T]TCATCCAGGGTGTTG | 9097 |
rs139817036 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP14 | GRCh38.p7 | 18:208988 | TGATCTCAAGTGATC[C/T]ACTCGCCCCGGCGTA | 9097 |
rs139886055 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:176413 | CCACCTTAGCCTTCC[A/G]ACTACCTTGGACTAC | 9097 |
rs139959080 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:162891 | CAACCTTCGCCTCCC[A/G]GGTTCAAGCGATTCT | 9097 |
rs139964295 | snp | A/C/G | 0.00163323 | 0.0285301 | missense | USP14 | GRCh38.p7 | 18:198077 | GCATCGGCAGCGACA[A/C/G]CTTCTAAAAAGAAAA | 9097 |
rs140029527 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP14 | GRCh38.p7 | 18:200077 | GTTCCTGCTTCACAC[C/T]GTGAAGAAGCACCTA | 9097 |
rs140103581 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP14 | GRCh38.p7 | 18:196849 | TACTGGAACATAGTT[C/T]GAAATATAAACATCA | 9097 |
rs140238083 | snp | A/T | 0.188316 | 0.242271 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157922 | CAATTTATATATATA[A/T]ATATATAAATATATA | 9097 |
rs140316667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:194179 | ATTTTTGATATTATA[A/G]ACAGGTTTCTTTTGT | 9097 |
rs140349579 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:197340 | TGCTTTTTTTCGCTT[C/T]ATAACCCTTATCTCT | 9097 |
rs140376024 | snp | A/C/T | 0.00755907 | 0.0610114 | intron-variant | USP14 | GRCh38.p7 | 18:164614 | GTCTACCACCATGCC[A/C/T]GGCTAATTTTTGTAT | 9097 |
rs140588176 | snp | A/C/T | 0.0131032 | 0.0799785 | intron-variant | USP14 | GRCh38.p7 | 18:170915 | ATGCTGGGCTTAATA[A/C/T]CTAGGTGATGGGTCT | 9097 |
rs140593132 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:159428 | AGGGTACTGGCCAGG[C/G]ATCACTTTTACTTAG | 9097 |
rs140639358 | snp | C/T | 0.000397184 | 0.0140867 | intron-variant | USP14 | GRCh38.p7 | 18:209937 | TTTTATTTCCAAAAT[C/T]ATGATTTAAAATTAA | 9097 |
rs140652336 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:173417 | TGCCCGGCCTATATT[A/G]TCTGTTTTTTTGAGA | 9097 |
rs140672218 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP14 | GRCh38.p7 | 18:172469 | AGCAGGATTTGAGAG[A/G]TTTGACTCCAGTTTC | 9097 |
rs140711496 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | USP14 | GRCh38.p7 | 18:207361 | TCAAAAAAGATTGAC[A/G]GGGATTACACGGAAT | 9097 |
rs140773458 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:204023 | TGGGAGGGGCCTATC[C/T]ATCATTTTAGCCTTT | 9097 |
rs140878922 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP14 | GRCh38.p7 | 18:173719 | TGAGCCACCGCACCC[A/G]GTCTATTATCTGTTT | 9097 |
rs140946465 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:210595 | TGGGTCTCAGAACCA[C/G]TTTACATTCTTGAAG | 9097 |
rs141000686 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:187816 | TATGAAAATTTTAAT[C/G]TAGTTTTTATTTACC | 9097 |
rs141056357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:206915 | CTCAGAGATTTATAC[A/G]TATGTTTTTTTCTGA | 9097 |
rs141060078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:192010 | GTTGTACTGTTGTAA[A/G]TTAAGTGAGGATCAT | 9097 |
rs141072027 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:197965 | ATTTTTAAAAAAATA[C/T]GTATTACTAAACTGG | 9097 |
rs141269921 | snp | A/G | 0.0002864 | 0.0119632 | intron-variant, missense | USP14 | GRCh38.p7 | 18:179002 | GCCAAAACTGTCTTC[A/G]TAGAAGACATGACAG | 9097 |
rs141291386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:193556 | TTTTAGAACATTATC[A/G]TTCCAAAAAGCAACT | 9097 |
rs141359358 | snp | C/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:176695 | TGTTAATATTTATGT[C/T]AGTTTTAGAAAATCT | 9097 |
rs141473480 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:174126 | TTGGAATTGCATTGA[A/G]TCTGTATGTCAGTCT | 9097 |
rs141563168 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | USP14 | GRCh38.p7 | 18:185253 | CAGCCTCTGCCTCCC[A/G]GCTTGAGCAATTCTT | 9097 |
rs141570639 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:166615 | TGGGATTACAGGCGT[C/G]AGCCACTGTGCCTGG | 9097 |
rs141608523 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:191296 | AGTCACATCAGTTTC[C/T]GAAAGATGCAAACAA | 9097 |
rs141709246 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP14 | GRCh38.p7 | 18:184816 | GTATAATGATGGAGG[A/G]TAGAAGGAAAGTGTG | 9097 |
rs141844059 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | USP14 | GRCh38.p7 | 18:189606 | TCCTACCACAGCCTC[C/T]TGAGTAGCTGGGACT | 9097 |
rs141890538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:205430 | TCTGCCCTACCCCTT[C/T]CTTAATTCCTGACAA | 9097 |
rs141917925 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:165059 | GCTCAAGTGACTGTC[C/G]TGCCTCAGTCTCCCG | 9097 |
rs141922666 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | USP14 | GRCh38.p7 | 18:200188 | TCCTTAGAGATAGTT[A/G]TTTTCATGGGCCCTA | 9097 |
rs141924448 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | USP14 | GRCh38.p7 | 18:162082 | GAGTTTCTTTCCTTT[C/T]TAAGGTTGAATAATA | 9097 |
rs141983940 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP14 | GRCh38.p7 | 18:205155 | TGCTGGGGATTATAG[A/G]CATGAGGCACCACAC | 9097 |
rs142009010 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:199372 | CATGTTTGCGAGTAA[A/G]CCAAAGTCATTATTC | 9097 |
rs142053454 | snp | A/G/T | 3.30089e-05 | 0.00406246 | missense | USP14 | GRCh38.p7 | 18:166800 | AGGATGATGATTGGG[A/G/T]AAACATCAAAATAAA | 9097 |
rs142080520 | snp | C/T | 0.00755907 | 0.0610114 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212992 | GGGATAAAATAAGCA[C/T]TGCAGGGAAACTTAT | 9097 |
rs142095417 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:169525 | AGTGTGGTTAATCTC[A/T]TTGATTTTTAACTTA | 9097 |
rs142147003 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:164343 | TGTACATGCATTTGT[A/G]TGTTGAAATTCAAAG | 9097 |
rs142220571 | snp | A/G | 0.000150965 | 0.00868675 | intron-variant | USP14 | GRCh38.p7 | 18:203223 | CTTTGTATAAGAAAT[A/G]TAATTCTTTGAAGGT | 9097 |
rs142255535 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-5-prime, downstream-variant-500B | USP14, LOC105371951 | GRCh38.p7 | 18:158494 | CCCAGTCTCCTCGCT[A/G]CAGTCGCTCCGGAGC | 9097 |
rs142318115 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:178462 | CCTTAAGCTTTATTC[A/C]GGTACAATTTATATA | 9097 |
rs142322160 | in-del | -/GG | | | intron-variant | USP14 | GRCh38.p7 | 18:206154 | TTTTCTAGAGTGGCT[-/GG]GTACCATTTTACATT | 9097 |
rs142349587 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | USP14 | GRCh38.p7 | 18:183471 | TCTTTAGGTACTGCT[G/T]CTCCTCCACCTGGTT | 9097 |
rs142423837 | snp | G/T | 0.0551013 | 0.156571 | intron-variant | USP14 | GRCh38.p7 | 18:181068 | CATGTTACAGCACAC[G/T]TAACACCTCATTCCT | 9097 |
rs142523870 | snp | C/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:176108 | TTATGATTTGTCTGT[C/T]TCCTCTATCATCAAG | 9097 |
rs142601914 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:197450 | CTGTTGAATGAATAA[C/G]CTATTCTAGAATGCT | 9097 |
rs142746853 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | USP14 | GRCh38.p7 | 18:195989 | ATTTTTTTTTTTCTT[A/C]TTGAGAGTCCAACAA | 9097 |
rs142818114 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | USP14 | GRCh38.p7 | 18:208777 | TTGAGACTGAGTCTT[C/G]CTCTGTCGCCCAGGC | 9097 |
rs142895352 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:183410 | GTGAGCACTTTTAGT[C/G]TGAGGACTCTTGTCG | 9097 |
rs143014424 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:195497 | GCTGTACATGAAGGA[G/T]GGCAAGGTATGATCA | 9097 |
rs143084306 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | USP14 | GRCh38.p7 | 18:206271 | TAGGTTTATAGTGAT[A/C]CTGTGTTTTCCTTTG | 9097 |
rs143109234 | snp | C/T | 0.000923178 | 0.0214648 | synonymous-codon | USP14 | GRCh38.p7 | 18:211227 | CTGGCATATCGCTTA[C/T]GTTCTACTCTATGGG | 9097 |
rs143184143 | in-del | -/T | 0.240478 | 0.249819 | intron-variant | USP14 | GRCh38.p7 | 18:172714 | TAGATGATTGTCAGC[-/T]TTTTTTTTTAAGCAA | 9097 |
rs143225059 | snp | C/T | 1.65173e-05 | 0.00287374 | missense | USP14 | GRCh38.p7 | 18:163371 | CAGATGAACCTCCAA[C/T]GGTATTCAAGGCTCA | 9097 |
rs143264510 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | USP14 | GRCh38.p7 | 18:176445 | GGTGTGTGCCACCAC[A/G]CATGGCTTGGTTTTA | 9097 |
rs143423200 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:193930 | CAAATGCTTTCATTT[C/G]TCTTTGGTATGCATC | 9097 |
rs143499599 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:171426 | ATGATGCTAAATCTA[C/T]TCTGCCTGTGCTCTG | 9097 |
rs143517597 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:160597 | GTTTTAATCTTCAAC[G/T]TAATCCTGTGATACT | 9097 |
rs143570401 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:184491 | GAGTGTGATGGCTCA[C/T]GCCTGTAATCCCAGT | 9097 |
rs143592409 | snp | A/T | 0.00358779 | 0.0422022 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212262 | AATGCAGTGATGTTA[A/T]CAGTCAGATTCTTTC | 9097 |
rs143658251 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | USP14 | GRCh38.p7 | 18:173401 | CAGGCTTGAGCCACC[A/G]TGCCCGGCCTATATT | 9097 |
rs143697685 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:196945 | TGGCTTCTGCCTTTG[C/T]CCCTTTGCAGTTTCT | 9097 |
rs143756666 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP14 | GRCh38.p7 | 18:198806 | TTAATTTTATAAAAG[A/G]GTGTGTATCAACTAT | 9097 |
rs143841401 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:209759 | AGGGTGTCTGTTACT[G/T]TACTGTAACAAGATT | 9097 |
rs143915535 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | USP14 | GRCh38.p7 | 18:186504 | ATGCTTGTAATCCCA[C/G]CACTTTGGGAGGCTG | 9097 |
rs144022744 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:191863 | TTAATCATAGTGTAT[A/G]TGCAGTCTCCCTCTC | 9097 |
rs144043673 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213507 | GTCTTTGAGAAGGGA[A/G]AGGAGTAGGCCAAAA | 9097 |
rs144117386 | in-del | -/ATC | 0.346811 | 0.230494 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213346 | TGTAATTAATTCCTT[-/ATC]ATCATCATTATAAAA | 9097 |
rs144167071 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212300 | CAGTTGTGTTTGTAT[G/T]TCCTTTCTTAATTCC | 9097 |
rs144180696 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | USP14 | GRCh38.p7 | 18:167320 | TAGTATATGTTCTTA[C/T]GCTCTCCAACTTTCT | 9097 |
rs144221246 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:169823 | TCATTACTCTCATGT[C/G]AAGTATGTTGATCTT | 9097 |
rs144230140 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:196564 | TTTGTTTGTATTAAT[G/T]AAAATTAATTTACAG | 9097 |
rs144290451 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:163513 | CTTTTTGAAAAATAA[C/T]GCCAGAAAATTATTT | 9097 |
rs144293279 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:208445 | ATTGGCTTTGTTTCA[C/T]GGATTTTTCTCTATT | 9097 |
rs144326546 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:166070 | TTGCTTTATAGATGC[A/G]TTATAGACATTAACT | 9097 |
rs144436115 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | USP14 | GRCh38.p7 | 18:173741 | TATCTGTTTTGAGTA[A/C]ATTCTTGTGTTTGCT | 9097 |
rs144514979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:173467 | CCCAGGCTGGAGTGC[A/G]ATGGCGTGATCTCAG | 9097 |
rs144625598 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:175742 | TAGGAAGCATCCCCT[C/G]TTTTCTGAGTTTGTA | 9097 |
rs144652496 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:188336 | ATTTTTCTCACTGGA[C/T]CTATTTGTGATACAT | 9097 |
rs144737796 | in-del | -/GATA | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:213978 | AGATAGATAGATTAG[-/GATA]ATAGATAGATAGATA | 9097 |
rs144742342 | snp | A/C | 0.0732091 | 0.177615 | intron-variant | USP14 | GRCh38.p7 | 18:173313 | AGACGGGGTTTCACC[A/C]TGTTAGCCAGGATGG | 9097 |
rs144756995 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | USP14 | GRCh38.p7 | 18:189434 | CAAATGTTGACAAAA[A/G]CCACTAGAAAGTCTC | 9097 |
rs144901470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:184928 | GGCTTGCTTAATGCC[A/G]CCCAACAGTGGAATC | 9097 |
rs144919318 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP14 | GRCh38.p7 | 18:192058 | TAGAAATCATTTAAT[A/G]GAAGCTTCTCAGTTT | 9097 |
rs144958426 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP14 | GRCh38.p7 | 18:173712 | ACAGGTGTGAGCCAC[C/T]GCACCCGGTCTATTA | 9097 |
rs145073320 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP14 | GRCh38.p7 | 18:205989 | TGGGTTGTTTCTAGT[A/G]TTTGTCTGTGATGAA | 9097 |
rs145131497 | in-del | -/AAAA | | | intron-variant | USP14 | GRCh38.p7 | 18:171023 | TTAAAAAAAAAAAAA[-/AAAA]TATATATATATATAT | 9097 |
rs145134015 | snp | A/G | 6.65956e-05 | 0.00577004 | synonymous-codon | USP14 | GRCh38.p7 | 18:209979 | TCCTCAGAGTGACAA[A/G]AAGAGTAGTCCCCAG | 9097 |
rs145171141 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | USP14 | GRCh38.p7 | 18:204866 | CATCCTCCATATATC[A/G]GTGCAGATCTTTAAA | 9097 |
rs145202182 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | USP14 | GRCh38.p7 | 18:170455 | AAGCCAAGACAGTCC[A/G]AAAGCTAGGCATTTT | 9097 |
rs145294436 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:189630 | TGGGACTACAGGCGC[A/C/G]TGTCACAACGCCCAG | 9097 |
rs145300023 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:209011 | CCGGCGTAAGCCACT[A/G]TACCCGGCCTAAATT | 9097 |
rs145382820 | snp | A/T | 0.190833 | 0.242898 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157966 | ATATATAAATATATA[A/T]AAATATATAAATATA | 9097 |
rs145417644 | in-del | -/AGTT | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214107 | GCTGGAGCCATAGAC[-/AGTT]AGTTAGTTAGTTATG | 9097 |
rs145455804 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:171304 | GAGAAGTCAGTGCCT[G/T]GGTTCAAAGGCCAGA | 9097 |
rs145490606 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | USP14 | GRCh38.p7 | 18:159436 | GGCCAGGGATCACTT[C/T]TACTTAGGGAATGGA | 9097 |
rs145528026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:209520 | ATTTCAGTTCATTTG[C/T]GCTGGCGTGGTAAGT | 9097 |
rs145556263 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:167754 | CTCCAGGGCTCAAGC[A/G]ATCCTCCTGCCTTGG | 9097 |
rs145665533 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:182950 | AAGTGTGGACTTCGT[A/G]TTGTGGGCGAAGAGA | 9097 |
rs145884268 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:165502 | AATTATAGAAGTATG[C/T]GAATTAAATGAAACT | 9097 |
rs145899952 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | USP14 | GRCh38.p7 | 18:169572 | GATGTGCAGTTCTCA[A/G]ATTTCTTGGTTTTGT | 9097 |
rs145900782 | snp | C/T | 0.00281237 | 0.0373935 | intron-variant | USP14 | GRCh38.p7 | 18:210044 | ATGGTAAGTAACATT[C/T]TCATTTTAATTGAGT | 9097 |
rs145934509 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP14 | GRCh38.p7 | 18:176180 | AAAAACATTTGGCCT[A/G]TTCATTTATTACTTC | 9097 |
rs145952708 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | USP14 | GRCh38.p7 | 18:180181 | TATATATGCCATGTC[A/C]TTTTGTAAAAATGGT | 9097 |
rs146178715 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:185540 | AAGAACTGAGACACT[C/T]GGAGAGAACAGAAAA | 9097 |
rs146296760 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:205171 | CATGAGGCACCACAC[C/G]TGGCCTTTAGGTGTA | 9097 |
rs146297254 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | USP14 | GRCh38.p7 | 18:162947 | GGATTACAGGCGTGC[A/G]CCACCACACCTGGCT | 9097 |
rs146316352 | snp | C/T | 0.00304029 | 0.0388703 | intron-variant | USP14 | GRCh38.p7 | 18:166862 | ATAATGCAGTAACCT[C/T]ATTATGATACCAAAA | 9097 |
rs146318211 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:183524 | AGATCTGTTTTTTAG[C/T]CTTCTAACTTTCCTC | 9097 |
rs146441567 | snp | C/T | 0.00478085 | 0.0486577 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213569 | ATATGCTGTGCCACT[C/T]ACACCGAGGCCATCA | 9097 |
rs146483426 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | USP14 | GRCh38.p7 | 18:159799 | AAATGCCAGCGCTGA[C/T]CAGAGTTTCTTTTTT | 9097 |
rs146562658 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP14 | GRCh38.p7 | 18:163604 | TTAAAACTGTCTTAT[A/G]CCTGTTAGAGTAAGG | 9097 |
rs146603574 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | USP14 | GRCh38.p7 | 18:174005 | AGTCTTCCAGTTGTT[C/T]TTCTTTTTTAAAGTT | 9097 |
rs146683649 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | USP14 | GRCh38.p7 | 18:176579 | TCTTATAGATTTGCT[G/T]TTTTGAGTGCTTAGT | 9097 |
rs146725150 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | USP14 | GRCh38.p7 | 18:194109 | GTATTGTATGTCTTT[C/T]TGACTATAGCCATCC | 9097 |
rs146804768 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | USP14 | GRCh38.p7 | 18:196983 | GCCCGCAATGTCCTT[A/T]TTAAAATGACGATAG | 9097 |
rs146823420 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | USP14 | GRCh38.p7 | 18:158950 | GGGGGGAGTGGAGAT[A/G]GGGAAGCCTCTCAAA | 9097 |
rs146845747 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:209852 | TAATTTGGAAGGTAG[A/C]CTGTATTTTGTCTCT | 9097 |
rs146919041 | in-del | -/TGATTGA | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214006 | TAGATAGATGATGAT[-/TGATTGA]TGATTGATGATTGAT | 9097 |
rs146922887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:160329 | AAAAAAGAAAATTAC[A/G]TATCTAGATTATTAA | 9097 |
rs146923144 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | USP14 | GRCh38.p7 | 18:203822 | TCACCGTGGTCTCAA[C/T]CTCCTGACCTCTTGA | 9097 |
rs146959256 | snp | C/T | 0.00224256 | 0.0334103 | missense | USP14 | GRCh38.p7 | 18:198132 | TTGAGTTTGAAACTA[C/T]GTATCCTTATGAGCC | 9097 |
rs147189013 | snp | C/T | 0.039522 | 0.134904 | intron-variant | USP14 | GRCh38.p7 | 18:173402 | AGGCTTGAGCCACCA[C/T]GCCCGGCCTATATTG | 9097 |
rs147205256 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | USP14 | GRCh38.p7 | 18:174932 | AGGAATGTGCCACCA[C/T]GCCGGACTAATTTTT | 9097 |
rs147209085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:209459 | AAGAGTCCTTGTCTA[A/G]TTTAAATCATACCTC | 9097 |
rs147471746 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:211488 | GGATTGTGCTGCCCT[A/G]TATAAAGGTGGCAGA | 9097 |
rs147562236 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:206006 | TTGTCTGTGATGAAT[A/G]AACCTGCTGTAAACA | 9097 |
rs147587530 | snp | A/G | 8.29758e-05 | 0.00644058 | missense | USP14 | GRCh38.p7 | 18:210001 | AGTCCCCAGAAAGAA[A/G]TTAAGTATGAACCCT | 9097 |
rs147598127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:203908 | GTTAAATCACTGGTG[C/T]CCAAAGAGTACTTAA | 9097 |
rs147647694 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP14 | GRCh38.p7 | 18:170627 | TTAAGTGGTGTGGAT[A/G]GAAGATCAAACTAGC | 9097 |
rs147735044 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP14 | GRCh38.p7 | 18:183423 | GTCTGAGGACTCTTG[C/T]CGCAAACTCTAGGAC | 9097 |
rs147750695 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:187435 | TAGTCATGTTCAATA[C/T]GCCTTTCTCCCTCTA | 9097 |
rs147838874 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | USP14 | GRCh38.p7 | 18:203758 | GGGACTACAGGCGCC[C/T]GCCACCGTGCCCGGC | 9097 |
rs147855606 | snp | C/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:205839 | TAATATAACCTTTCT[C/T]ACTCAGCATAATTCT | 9097 |
rs147982314 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:190340 | TATATGAGTGAAACT[A/G]CTGGGTCATAAAAGG | 9097 |
rs148032911 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:184588 | GCAAAACCCCACCTC[C/T]ACAAAACAGACAAAC | 9097 |
rs148229204 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP14 | GRCh38.p7 | 18:195931 | TTGTTTACAGCTAGT[A/G]ATTGCTTTGTAAGGT | 9097 |
rs148317164 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:208706 | TCTAGTTTGATGCCA[G/T]TGTGGTGACAGAACA | 9097 |
rs148368302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:174562 | TAAGCCACTGCACCC[A/G]GCTTATTTCATGGTT | 9097 |
rs148474324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:176068 | GTAGTGCTGCTTTTT[C/T]GTTTTCCTCTCTAGT | 9097 |
rs148494862 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | USP14 | GRCh38.p7 | 18:167807 | CAGGTGTGAGTCACT[C/G]TGCCCAGCCCTTGCA | 9097 |
rs148509892 | snp | A/G | 0.0191346 | 0.0959228 | intron-variant | USP14 | GRCh38.p7 | 18:192802 | TTGAGTGTTAGAATG[A/G]ATTGAATTCTATTGT | 9097 |
rs148685128 | snp | A/G | 0.0174175 | 0.0916809 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212911 | CTGATGATAACTATT[A/G]AAAATAGAAAATAAC | 9097 |
rs148720233 | snp | A/G | 0.0123036 | 0.0774623 | upstream-variant-2KB, nc-transcript-variant | USP14, LOC105371951 | GRCh38.p7 | 18:158143 | TTTATTTTGAGGCAG[A/G]GTCTCGCTCTGTCGC | 9097 |
rs148752127 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | USP14 | GRCh38.p7 | 18:169895 | ACCTGTAAGATGGCA[A/G]ACTTAATCGACAAAT | 9097 |
rs148827619 | snp | G/T | 0.0322114 | 0.122752 | intron-variant | USP14 | GRCh38.p7 | 18:160221 | AGGCAGGAGAATCGC[G/T]TGAACCTGTGAAGCG | 9097 |
rs148846817 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | USP14 | GRCh38.p7 | 18:209703 | TGCTGTATTCACTGG[G/T]ACGCTTTCACTTTAA | 9097 |
rs148862487 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:171376 | GTTGAAACCAATGCT[C/T]GTTTACCATTCCAAA | 9097 |
rs148950324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:184126 | AAGTATTTTTTGTTT[C/T]TCCTTTTTTTAAAAA | 9097 |
rs149021502 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:206018 | AATAAACCTGCTGTA[A/G]ACATTCGTGTACAGG | 9097 |
rs149038606 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | USP14 | GRCh38.p7 | 18:194853 | CGAGAATCGCTTGAA[C/T]CTGGGAGGCAGAGGT | 9097 |
rs149087925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:163687 | TTTAAAACTCTTTTT[A/G]CTTTTGTTTATTTTT | 9097 |
rs149092072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:189223 | AGATTTGTTCATTCA[A/G]TTTTTTGAGTTGTCT | 9097 |
rs149286691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:175168 | CTGTGACTTTATTTC[A/G]TATATTAATTTCTTA | 9097 |
rs149412129 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | USP14 | GRCh38.p7 | 18:198515 | TGAGCCACCGCGCCC[A/C]GCCCAGAGGTTTTTA | 9097 |
rs149483154 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | USP14 | GRCh38.p7 | 18:186421 | TGATGATGCCACTGC[A/G]CTCCAGCCTGGGCAA | 9097 |
rs149551254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:208392 | TGTGTTTGTCCCCCT[C/T]GCTTGAGGATTATTA | 9097 |
rs149604092 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP14 | GRCh38.p7 | 18:204806 | AGAACTATACTTTGT[A/G]TAGTATTATTTGGAT | 9097 |
rs149620609 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:165599 | AATTCTCAGCTGTAT[C/G]TTATCCATATCTTAT | 9097 |
rs149659367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:209480 | ATCATACCTCTTTAA[C/T]GTAGGTAAGTCTTTG | 9097 |
rs149709610 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | USP14 | GRCh38.p7 | 18:205580 | GGAGTTCGAGACTGT[C/G]CTGGGCAACGTAGTG | 9097 |
rs149725854 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | USP14 | GRCh38.p7 | 18:167720 | GGGGTGTCACTATGT[C/T]GCCCAGGCTGGTCTT | 9097 |
rs149779470 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | USP14 | GRCh38.p7 | 18:162938 | GAGTAGCTGGGATTA[C/T]AGGCGTGCGCCACCA | 9097 |
rs149784611 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:187011 | AGATATTGGCAGTTG[-/T]TTATCCCAAAAGGTA | 9097 |
rs149818369 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | USP14 | GRCh38.p7 | 18:176811 | TTGTGGTATGGTATG[A/C]AGTAGAGAGCTGATA | 9097 |
rs149868837 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:173555 | TAGCTGGGATTAAAG[A/G]CATGCACCACCACAC | 9097 |
rs149939928 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | USP14 | GRCh38.p7 | 18:201968 | TGCTGAATAAACTTG[C/G]TTAAATGTTAAAAAG | 9097 |
rs150097778 | in-del | -/TTTATTTTAT | 0.214843 | 0.247516 | intron-variant | USP14 | GRCh38.p7 | 18:200781 | TGATAATTAGGATTG[-/TTTATTTTAT]TTTATTTTATTTATT | 9097 |
rs150098659 | snp | A/G | 0.000481754 | 0.0155127 | intron-variant | USP14 | GRCh38.p7 | 18:197730 | TGATTATAGACTTTC[A/G]TTATACCTTGATTTT | 9097 |
rs150167598 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:159927 | CTCCATATTGAGAAT[C/G]TGTATTTTGAGGGTC | 9097 |
rs150187010 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:210616 | ATTCTTGAAGCCCCA[A/G]AGAGCTTTGGTTTAT | 9097 |
rs150203014 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP14 | GRCh38.p7 | 18:173268 | GCCTGCCACCACACC[C/T]GGCTATTTTTTTTGT | 9097 |
rs150379203 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | USP14 | GRCh38.p7 | 18:194384 | TAATAGTATTGATGC[A/G]ATGAAAAATACTGTT | 9097 |
rs150429639 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | USP14 | GRCh38.p7 | 18:188958 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGTGCT | 9097 |
rs150469328 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:204091 | GCGTTGTATGAGAAG[G/T]TTAAATGTAGTTGAA | 9097 |
rs150540490 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP14 | GRCh38.p7 | 18:191649 | TCTGAAACGTAAAAT[A/G]AACGGAATCCTACAG | 9097 |
rs150628158 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | USP14 | GRCh38.p7 | 18:205456 | GACAACTACCAACCC[G/T]TTCATTTCTATAATT | 9097 |
rs150680846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:199804 | AAGGTTATGTATTGA[C/T]TGGTTGATGAAAATG | 9097 |
rs150697196 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP14 | GRCh38.p7 | 18:162443 | AAATGATTTAGATAT[A/G]TCTTTGGATTTTTTC | 9097 |
rs150701945 | snp | A/C | 0.000148609 | 0.00861873 | missense | USP14 | GRCh38.p7 | 18:198075 | CTGCATCGGCAGCGA[A/C]ACCTTCTAAAAAGAA | 9097 |
rs150716057 | snp | A/G | 0.0138799 | 0.0821421 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213091 | AGAATAGAATGGGCA[A/G]GATGAGACCATGAAA | 9097 |
rs150839462 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | USP14 | GRCh38.p7 | 18:170160 | AAATAGAAAAATAGC[C/T]GGGCGTAGTGGCACA | 9097 |
rs150946501 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:171575 | TTATTGACAATGCAT[A/C/G]TAGTCACTTAAGAGT | 9097 |
rs151071080 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | USP14 | GRCh38.p7 | 18:193180 | ATCTTTGGGGTTGAC[C/T]CTGGGGATAGCCAGC | 9097 |
rs151160978 | in-del | -/AGAT | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:213972 | TTTCTGTAATGGACA[-/AGAT]AGATAGATTAGATAG | 9097 |
rs151227286 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:164422 | TTTTTTTTTGGCCTT[C/T]ATTGCATCCTACCCA | 9097 |
rs151228980 | snp | A/G | 0.00014844 | 0.00861383 | synonymous-codon | USP14 | GRCh38.p7 | 18:210474 | AGGTCATTATGTATC[A/G]TGGGTGAAAAGGAAA | 9097 |
rs151245031 | snp | C/T | 0.210605 | 0.246877 | intron-variant | USP14 | GRCh38.p7 | 18:188708 | TTTGAGACAGAGTCT[C/T]GCTGTGTTGCCCAGG | 9097 |
rs180839084 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:207939 | TGGATCTTAAATCCT[G/T]GACTTTGCTGAATTT | 9097 |
rs180850309 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:189694 | CATCATGTTGGCCAG[A/G]ATGGTCTCGATCTCT | 9097 |
rs180869346 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:171908 | TCAAAACTTGAGTTG[A/T]GGATACAACTGCACA | 9097 |
rs180879168 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:181550 | AAAAATTCAATTGTG[G/T]TTTTACATATATACA | 9097 |
rs180920667 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:165287 | TAGCTTTAAAAAATA[C/G]TTCCTTCAAGGGTTA | 9097 |
rs180989296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:199471 | AGTCCCATCTGAGGT[C/T]AAACAAGTACTTGGC | 9097 |
rs181086784 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP14 | GRCh38.p7 | 18:168221 | GTGAGCCACCGCACC[C/T]GGCCAAAATACAGTT | 9097 |
rs181153436 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:185545 | CTGAGACACTCGGAG[A/T]GAACAGAAAAGCCCC | 9097 |
rs181207838 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:194904 | TCAGTGTACTCCAGC[C/T]TGGGCAACAGACTGA | 9097 |
rs181214792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:203269 | ATTGCTTTCATTATT[C/T]CTTTAGGAATAGTTA | 9097 |
rs181231604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:176353 | AGATGGGGTCTTGCT[A/G]TGTTGCTGAGGCTGA | 9097 |
rs181239728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:159413 | GCTTGCTGACAGTCC[A/G]GGGTACTGGCCAGGG | 9097 |
rs181392637 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:190887 | AATGGATGGTTTTAC[A/C]TGAATTAGGAATTAC | 9097 |
rs181411714 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:173018 | GTTGTAAGAAATCTT[A/C]GCCTGTGCCAAGTTT | 9097 |
rs181459529 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:164566 | TCAAGCGATTCTTAT[C/G]CCTCAGCCTCCTGAG | 9097 |
rs181573697 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:209239 | GCTGTAGGTGATTTC[A/G]TTATCTGTATAAAAA | 9097 |
rs181602802 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:180047 | AATATGATGGCCAGC[A/G]TGATCCAAGTAAACT | 9097 |
rs181612315 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:175419 | TCAGGTTCAGGAACT[C/G]TTTCTAGTTTGCTGA | 9097 |
rs181627027 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:159139 | GCGACCCTTCTTGGG[G/T]TTGCCAAGCGGCGTT | 9097 |
rs181814833 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:179515 | GAAACTGGTCAACAC[A/G]TGTCAATTTTTTTTT | 9097 |
rs181967145 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP14 | GRCh38.p7 | 18:172387 | CTCCTAGTGAAGAAG[C/T]TGTGAATGTTGTTGA | 9097 |
rs182003691 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:203910 | TAAATCACTGGTGCC[C/G]AAAGAGTACTTAAAT | 9097 |
rs182023971 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:168838 | AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA | 9097 |
rs182041948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:208286 | ATCAAATTTGTATGT[A/G]GAATTGTTTCTAGTA | 9097 |
rs182124906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:205840 | AATATAACCTTTCTC[A/G]CTCAGCATAATTCTC | 9097 |
rs182129748 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:171217 | AGCTACACTATACAA[C/T]AGATTTTCAGTGTGG | 9097 |
rs182132424 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:188721 | CTCGCTGTGTTGCCC[A/G]GGCTGGAGTGCAGTG | 9097 |
rs182222059 | snp | A/G | 0.0193772 | 0.0965046 | upstream-variant-2KB, downstream-variant-500B | USP14, LOC105371951 | GRCh38.p7 | 18:158212 | AGCCTCGACCTCCTG[A/G]GCTCAAGCGATTCTC | 9097 |
rs182315488 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:189916 | GCACTCTAAAAATCC[C/T]CTCACAGATCTTAAT | 9097 |
rs182315910 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:193639 | CTATGTGTTATTTCT[C/T]TCTAGATTTGCCTAC | 9097 |
rs182346253 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:209599 | GAGGTAGTTGTTTTT[C/T]CCCCCCACCTCTGTG | 9097 |
rs182370631 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:166621 | TACAGGCGTGAGCCA[C/G]TGTGCCTGGCCAAAA | 9097 |
rs182376790 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP14 | GRCh38.p7 | 18:173263 | CAGGTGCCTGCCACC[A/G]CACCCGGCTATTTTT | 9097 |
rs182378004 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:191184 | TAAAATGTCTTAACA[A/G]GGAAATGTAATGATT | 9097 |
rs182586062 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | USP14 | GRCh38.p7 | 18:188067 | GTTAAATAGTAGATG[A/G]TTGTGGAATTCTCTC | 9097 |
rs182592565 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:174466 | AGACGGGGTGTCACC[A/G]TGTTGGTCAGGCTGG | 9097 |
rs182596665 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | USP14 | GRCh38.p7 | 18:170118 | TCAGCCTGGCCAATA[C/T]GGTGAAACCCCATCT | 9097 |
rs182599052 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214124 | TTAGTTAGTTAGTTA[C/T]GAGTGAGCACAGCTG | 9097 |
rs182627268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:183287 | TCAGTCTTGATTTTT[A/G]TTCTTTTCTGTTAGT | 9097 |
rs182920641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:201548 | GGAGAGTTTTGAGCC[A/G]GTGTGGATATGAACA | 9097 |
rs182934868 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:196481 | GTGAGCCGAGATCGC[A/G]CCACTGCACTCCAGC | 9097 |
rs182954222 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:177484 | CTTTACTGCTTTGCA[A/G]TGATCTTATAAAATG | 9097 |
rs182970485 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP14 | GRCh38.p7 | 18:161207 | TGCTGGGATTACAGG[C/T]ATGAGCCACCATTCC | 9097 |
rs183157586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:200676 | GTGTGCTTTGGGGAT[A/G]TGTATATCTCTCGAA | 9097 |
rs183168602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:165926 | TAAAAGGGAGTAATA[C/T]AGAATCGACTTTATC | 9097 |
rs183173459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:165840 | ACCGTTCCATTTTAA[A/G]GCAGATAAAAGAGAT | 9097 |
rs183250904 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:200879 | CAATCTCGGCTCACT[A/G]CAACCTCTGACTCCC | 9097 |
rs183493837 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:182552 | ATATATTATCAGTGA[A/C]CAAGACACAGTATCT | 9097 |
rs183523612 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | USP14 | GRCh38.p7 | 18:189887 | ATACCCAAAATAAAG[G/T]CAGAACCCTTCTAGC | 9097 |
rs183533142 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:208077 | ACTTTCAGGAGTTTT[A/G]TTTGTTTATTTTATT | 9097 |
rs183631698 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | USP14 | GRCh38.p7 | 18:162452 | AGATATGTCTTTGGA[C/T]TTTTTCTTAATTGAG | 9097 |
rs183688794 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | USP14 | GRCh38.p7 | 18:169911 | ACTTAATCGACAAAT[A/G]TGTCTTCTGACAGCC | 9097 |
rs183753203 | snp | C/T | 0.00795532 | 0.062565 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212685 | GTAGAAAATACCAAG[C/T]ATATGAGGTATTTCA | 9097 |
rs183758244 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:173304 | TTTTAGTAGAGACGG[G/T]GTTTCACCATGTTAG | 9097 |
rs183766525 | snp | C/T | 0.000104185 | 0.00721675 | missense | USP14 | GRCh38.p7 | 18:204583 | TTAAATTTCCTCTTA[C/T]GTTGGATATGTATGA | 9097 |
rs183850089 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:210291 | TTCTGATAATACTTT[C/T]GTAATGTGAACTTTA | 9097 |
rs183946089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:207198 | CCTGATGCTCATACC[A/G]GACTGACTTGATTAC | 9097 |
rs183970898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:171663 | GCAGCCCATGGATCA[A/G]TAATTTCTACTTTTA | 9097 |
rs183974410 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:191890 | TCTCACTTCAGTGTT[G/T]GATATTAACTGAATG | 9097 |
rs183979004 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:189352 | ATTGTTTACTTACCC[C/T]TGTGTAGTAATGAAA | 9097 |
rs184066575 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:195597 | ATGCTGCTGAGAGGG[G/T]TAAGTGGAAAGAAGG | 9097 |
rs184072195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:160484 | TCTGTGATCACGCCA[C/T]TGCACTCCAGCCTGG | 9097 |
rs184131717 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:197778 | CCCTCAAAGGCTTAA[A/T]ATAAGTTCCATCTTA | 9097 |
rs184168739 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:210939 | GCTCTAGTGGTGTCA[C/T]TGAAGTAGTTGTAAC | 9097 |
rs184175460 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:192482 | GGCAGGAGAAATTGC[G/T]TGAACCCAGGAGGTA | 9097 |
rs184192770 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | USP14 | GRCh38.p7 | 18:173370 | CCCGCCTTGGCCTCC[C/T]AAAGTGCTGGGATTA | 9097 |
rs184199838 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:176696 | GTTAATATTTATGTC[A/C]GTTTTAGAAAATCTT | 9097 |
rs184205562 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:156876 | TTGAGACCAGGAGTT[A/C]AACACCAGCCAGGGC | 9097 |
rs184254563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:179361 | CTGGCAGATAGTACT[A/G]TATAAGTATTTACTA | 9097 |
rs184401021 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157455 | AACAGTGTTCACAGC[A/G]TCTTCACCAGGAGTA | 9097 |
rs184480970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:193333 | ATTGCATAAGAGAAT[A/G]TAACCCCCACCTAAT | 9097 |
rs184534679 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:174068 | TTGCACATTTTTAGA[G/T]TCTGCTTGTCATTTT | 9097 |
rs184657129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:179612 | TTTTTCCTTGAGATG[A/G]GGTCTTGCTCTGTCA | 9097 |
rs184667382 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:163794 | TTCATCACCCAGGTA[C/G]TAAGCATAGTACCCG | 9097 |
rs184749923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:177993 | AGACATTCACAGAAA[C/T]AATTTTATTAGTGTT | 9097 |
rs184799224 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:161654 | ATGAATACTCAACAT[A/G]TTAATTGAACTGATG | 9097 |
rs184862776 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | USP14 | GRCh38.p7 | 18:197065 | CTAAATCCTCTAGCC[C/G]CTGGCTTTCTCTCTG | 9097 |
rs184891972 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP14 | GRCh38.p7 | 18:184453 | TCTTTGGCAGGTTCT[A/G]TAGAGTGGGAGGTAT | 9097 |
rs184906222 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:167466 | TTTAGGTCTCTGTTT[G/T]TCTCTTAGCAGAGTT | 9097 |
rs184907660 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:201877 | ATGTATTTATTTCCT[C/T]TATAACTTTTAAGAT | 9097 |
rs184975352 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:181786 | GCTTTTGGTTTCATA[C/T]GTAAAAGCCATTGTC | 9097 |
rs184979420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:165408 | GTTTACCCCCGAAGG[C/T]ACAGTATGAACCTTT | 9097 |
rs184993102 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:206828 | ATCGCTTGAACTGGG[A/G]AGGCAGAGGTTGTAG | 9097 |
rs185057299 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:202810 | TTAAAAGGCTTACTG[G/T]TGTGATTCTATATTG | 9097 |
rs185103252 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:185105 | CCAGCTCTCAATATA[C/T]ACAGCGTTAACAGTT | 9097 |
rs185195469 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:168566 | CAACCTCCTGAGTAG[C/T]TGGGATTACAAACGC | 9097 |
rs185210101 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:185590 | AGCTGTCTAGGGGAT[A/G]TGTTCATTGAGTGGA | 9097 |
rs185238498 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:188925 | CTCAGGTGATCCCCC[G/T]GCTTTGGCCTCCCAA | 9097 |
rs185357604 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:171569 | TACTGCTTATTGACA[A/G]TGCATCTAGTCACTT | 9097 |
rs185420335 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:206492 | CCTAGTCTGTAGCTT[A/G]TGTTTTCATCCTCTT | 9097 |
rs185522383 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214142 | GTGAGCACAGCTGGG[C/T]GCCAGTACAATTTTA | 9097 |
rs185636986 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:193896 | ACTCCTGACAGTCGT[G/T]TACAAGTCTTGGTGT | 9097 |
rs185669605 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP14 | GRCh38.p7 | 18:158882 | CCCCTCTCCCGGCTG[A/G]GTCGGAGCCCTGCGT | 9097 |
rs185741257 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:209301 | TGTGGAATCCTTTGA[C/T]TTCTTGCCATCACAG | 9097 |
rs185743745 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP14 | GRCh38.p7 | 18:173164 | CCCAGGCTGGAGTGC[A/G]GTGGCACGATCTCGG | 9097 |
rs185751041 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP14 | GRCh38.p7 | 18:190919 | TTTTATTGCTCTAAT[A/G]TGGGAATTTTTTTTT | 9097 |
rs185762502 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:172237 | AGTGAGACCCTGTAT[C/T]TAAAAAACGAAAAAG | 9097 |
rs185811948 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP14 | GRCh38.p7 | 18:200250 | ATTACTTAATCTAAG[C/G]TACTGTTTTCTTACG | 9097 |
rs185965324 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:165898 | AAGCATATTGGGTAC[C/T]CGATACCTTCTATAA | 9097 |
rs185975686 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:182156 | CGTATGAAAGGAAAA[G/T]AGTAAAGAATTAATT | 9097 |
rs185990595 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP14 | GRCh38.p7 | 18:176200 | TTTATTACTTCGTTT[A/G]TTTTTTCTCTTTGCT | 9097 |
rs185992329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:194562 | CATTTTAGAATAAGG[C/T]GCCAGACATCCTGAA | 9097 |
rs186042559 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:200714 | CCCATTTGAACTGAT[A/G]CCTTTTAATAGTTTT | 9097 |
rs186069991 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:194995 | AATACAGTCTTTATT[C/G]AGATTTTGCCAACTG | 9097 |
rs186071920 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:159509 | TGTGTGGTGTCTCCA[A/G]TTGGCTGTAGGTGTG | 9097 |
rs186209493 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | USP14 | GRCh38.p7 | 18:176386 | TTGAGCACCTAGGCT[C/G]AAGCAGTACTCCCAC | 9097 |
rs186213235 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | USP14 | GRCh38.p7 | 18:169315 | GCAGTGAGCTGAGAT[C/G]ACACCACTGCACTCC | 9097 |
rs186280218 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:204102 | GAAGGTTAAATGTAG[A/T]TGAAGTATCTAGTGT | 9097 |
rs186324880 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:180517 | AACCATCACCACCAT[C/T]GATTTTAGGACATTT | 9097 |
rs186498286 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:199012 | TTTATTACTCATTGT[G/T]GTTTCTAGAATTGTT | 9097 |
rs186502317 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | USP14 | GRCh38.p7 | 18:164626 | GCCCGGCTAATTTTT[G/T]TATTTTTAGTAGAGA | 9097 |
rs186617945 | snp | A/G | 0.000148582 | 0.00861795 | missense | USP14 | GRCh38.p7 | 18:204646 | TGTCTTTTCGATCCA[A/G]ATTCAAGGATCTAGA | 9097 |
rs186634805 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:169919 | GACAAATGTGTCTTC[G/T]GACAGCCTCACCGAC | 9097 |
rs186725449 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:183403 | GTACTCAGTGAGCAC[G/T]TTTAGTCTGAGGACT | 9097 |
rs186732868 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:209642 | TTTGGTAACACTGGG[A/G]AATTGGGTTTTTCCT | 9097 |
rs186734640 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:166903 | ATGACTTTTTTTCAT[G/T]TGTATATCCAGTTGT | 9097 |
rs186741205 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:201579 | TGGTGACTTTTAAGA[G/T]AAATTCATTTAAAAA | 9097 |
rs186831471 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:187309 | GGTCTGATTTTCGAT[A/G]TGTGTTTGTATTATG | 9097 |
rs186873536 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:189940 | TCTTAATCACTAACA[C/T]CGTTTATGTTTCCCA | 9097 |
rs186959967 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP14 | GRCh38.p7 | 18:188257 | ATTTGTTTACTGGAG[A/G]TTTTTTAAAAATAAG | 9097 |
rs186973927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:170365 | CTAAGTGTTCAAGAG[A/G]AAGGAAGAGTTTCAT | 9097 |
rs186974871 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP14 | GRCh38.p7 | 18:205474 | CATTTCTATAATTTT[C/T]GTCATTTCAAGAAAG | 9097 |
rs187023555 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP14 | GRCh38.p7 | 18:173468 | CCAGGCTGGAGTGCA[A/G]TGGCGTGATCTCAGC | 9097 |
rs187036523 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:156916 | AAATCCCGTCTTTAC[A/G]AAACATACAAAAAAA | 9097 |
rs187081582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:172858 | TGACTTGCTTTATTG[C/T]GATATTTGCTTTCTC | 9097 |
rs187082914 | snp | A/G | 0.00015299 | 0.00874479 | intron-variant | USP14 | GRCh38.p7 | 18:211127 | CTTCTTGTCCCTGTT[A/G]TTTAGATGAATGGAT | 9097 |
rs187087298 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | USP14 | GRCh38.p7 | 18:192744 | CTGAGAAACTTGCAG[C/T]TGAGGGTGTCATAAG | 9097 |
rs187096435 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:208541 | TTTCCCTTTCAGCAG[A/T]GATTTCACTATATCC | 9097 |
rs187246639 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:161360 | ACACCATGCTGCTTT[A/T]TGCTGTGGAATGTTT | 9097 |
rs187255461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:177704 | TGTTCATGCCTTCCA[A/G]TTAAGATACTGAGTA | 9097 |
rs187310161 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:196906 | TCTCTTGCCTGGAGC[C/T]GCACAGTAGTCTTAA | 9097 |
rs187496577 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | USP14 | GRCh38.p7 | 18:173265 | GGTGCCTGCCACCAC[A/G]CCCGGCTATTTTTTT | 9097 |
rs187727329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:197210 | GATAAGTGCAAGACC[A/G]GCTCCCTCACCTCCT | 9097 |
rs187744346 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:191586 | CAGTTAATCCTTATC[C/G]TCTCCACCCCCTTCC | 9097 |
rs187764255 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:161852 | TTATGAGGCTGATTG[A/G]AATTTTTTATTGTGG | 9097 |
rs187785374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:176803 | AATTGTTGTTGTGGT[A/G]TGGTATGAAGTAGAG | 9097 |
rs187802823 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:160573 | TTAGGGTTTTGTACA[A/T]ATTGCTTTGTTTTAA | 9097 |
rs187909990 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP14 | GRCh38.p7 | 18:206055 | TGTAAACGTAAGTTC[C/T]ATTTCTCTGGAATGA | 9097 |
rs187989236 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:182846 | CTGCAACATACTCAG[G/T]GCAACTGCCTGGAGA | 9097 |
rs188030197 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:178150 | TTTAGCCCCCAAGTA[G/T]CTGGGACTACAGGCA | 9097 |
rs188057286 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:168579 | AGTTGGGATTACAAA[C/T]GCCTACCACCATGCC | 9097 |
rs188067591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:185627 | TGTGGGATTGCTTAC[A/G]CTACTTAAATTATTT | 9097 |
rs188132089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:203840 | CCTGACCTCTTGATC[C/T]GCCCGCTTTGGCCTC | 9097 |
rs188286014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:207015 | AGGTGTGGGTTCAGA[C/T]TCATTGTTTTGCATG | 9097 |
rs188286148 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP14 | GRCh38.p7 | 18:201043 | CCTGACCTTGTGATC[C/T]GCCCACCTCGGCCTC | 9097 |
rs188297031 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:166166 | GATCTATCATTTGTC[A/G]TTAGTCAAGTGTTTT | 9097 |
rs188306024 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:171904 | GAGTTCAAAACTTGA[G/T]TTGAGGATACAACTG | 9097 |
rs188377009 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:207334 | TATTTTAGGATCAGC[G/T]TGTCCATTTCTTCAA | 9097 |
rs188385511 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP14 | GRCh38.p7 | 18:189503 | TTTGTTTTTTTTTTG[A/G]GAAGGAGTCTCACTC | 9097 |
rs188563895 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:191986 | AAAAGGAATTTGCAT[A/G]GCCAGTTTGTTGTAC | 9097 |
rs188796430 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | USP14 | GRCh38.p7 | 18:188747 | CAGTGGCATGATCTC[A/G]GCTCACTGCAACCTC | 9097 |
rs188819456 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:190133 | TCGTTTATATTCATG[C/G]TATATAGTATAGTAT | 9097 |
rs188833686 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:173305 | TTTAGTAGAGACGGG[A/G]TTTCACCATGTTAGC | 9097 |
rs188992969 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:198771 | GTTAATAATAACTTT[C/T]AAAATAAAAAAAGAA | 9097 |
rs189067955 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:195943 | AGTGATTGCTTTGTA[A/G]GGTCTTCTGGTGAGT | 9097 |
rs189076051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:171358 | TGTAGCTAATGACTT[C/T]AAGTTGAAACCAATG | 9097 |
rs189092697 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213698 | CTTCAGGATTAAAAA[C/T]GATGATGACCTCATC | 9097 |
rs189110792 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:174345 | ATCTCAGCTCACTGC[A/G]GACTCCGCCTCCTGG | 9097 |
rs189225788 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:159047 | GGGCGCTGGGCCAGG[C/T]TGGAGGTGCAGGGAG | 9097 |
rs189233178 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:202014 | TCCTTTTGTAATATG[A/C]TTAGTAATTTTAAAA | 9097 |
rs189243284 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:184995 | CCTAGAGTGAAAACT[A/G]TATGTTATAAAAAAA | 9097 |
rs189310678 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:175351 | TGCCTTTTTCCTGAC[C/T]TTAGGGGAAAAGCCT | 9097 |
rs189360954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:193569 | TCATTCCAAAAAGCA[A/G]CTTCATAACATCTAG | 9097 |
rs189383743 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:199070 | GTTGAAATGAATCTT[A/G]GGAGACTAAAAGGTT | 9097 |
rs189385576 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157924 | ATTTATATATATATA[C/T]ATATAAATATATATA | 9097 |
rs189476389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:162481 | AGCACCTCTTGTTCA[A/G]AAATGACACTTTTCA | 9097 |
rs189544026 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:179440 | ATATTTAAATTTTTA[A/G]AATCCTTCATGTGGA | 9097 |
rs189562044 | snp | C/T | 3.29989e-05 | 0.00406182 | synonymous-codon | USP14 | GRCh38.p7 | 18:198112 | AATCGATCAGTTCTT[C/T]GGTGTTGAGTTTGAA | 9097 |
rs189677037 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:185340 | ATTTTTGTATTTTTA[G/T]TAGAGACGGGTTTTG | 9097 |
rs189695121 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:181347 | AATTGCCAATATTGT[C/G]TGTCTTTGATTAAGC | 9097 |
rs189905210 | snp | A/T | 0.00160297 | 0.0282651 | intron-variant | USP14 | GRCh38.p7 | 18:203073 | TTTTGATGTAATGGG[A/T]TTTCTTTACATTTTG | 9097 |
rs189936720 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:171627 | GAATGTTGTTTTCCT[G/T]TCTGCTACAACAACT | 9097 |
rs189943506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:168012 | GCGCGATCTCGGCTC[A/G]CTGCAACCTCTGCCT | 9097 |
rs190062299 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP14 | GRCh38.p7 | 18:209355 | TCTTCATTACCATTA[C/T]AGTTTTAAAGAACTT | 9097 |
rs190064655 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:173215 | CTGGTTCACGCCATT[A/C]TCCTGCCTCAGCCTC | 9097 |
rs190068726 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:191112 | AAGTGATGTTCAGGG[C/T]ATGTCTGCTATATTA | 9097 |
rs190156566 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP14 | GRCh38.p7 | 18:167580 | GCATGGTCATGGCTC[A/G]CTGCAGCTTTAAACT | 9097 |
rs190157339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:164536 | TTGGCTCACTGCAAC[C/T]TCCGCCTCCTGGGTT | 9097 |
rs190184119 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:188928 | AGGTGATCCCCCGGC[C/T]TTGGCCTCCCAAAGT | 9097 |
rs190236018 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:193944 | TCTCTTTGGTATGCA[G/T]CTAGGAGTGGAGTTA | 9097 |
rs190313444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:194892 | GCTGAGATTGTGTCA[A/G]TGTACTCCAGCCTGG | 9097 |
rs190315583 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | USP14 | GRCh38.p7 | 18:176238 | TTTCTACTTCGGTTT[A/T]AAATTTTTTAAAATT | 9097 |
rs190444428 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP14 | GRCh38.p7 | 18:189904 | AGAACCCTTCTAGCA[C/G]TCTAAAAATCCCCTC | 9097 |
rs190451243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:200808 | TATTTTATTTATTTA[C/T]TTACTTATTTTGAGA | 9097 |
rs190478689 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214220 | TCTGCTTGAAAGCAC[A/G]AATAAGTGAGAACAG | 9097 |
rs190627547 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:173002 | TAGTGATTTGTACTA[C/T]GTTGTAAGAAATCTT | 9097 |
rs190699314 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:204290 | TTCTTTTCTCAGGTA[A/C]ATTTTGGTACTTCCT | 9097 |
rs190703335 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:177227 | TATTGCTAGTGTATT[A/C]TTTAAATAGTTGGCT | 9097 |
rs190710567 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:208208 | GGCTATTCAAATGAT[A/C]TATTTCATATTGTGT | 9097 |
rs190719674 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP14 | GRCh38.p7 | 18:161206 | GTGCTGGGATTACAG[A/G]CATGAGCCACCATTC | 9097 |
rs190720322 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:172304 | CCACAATCTCATGAT[A/G]CAACTTGAACAGATG | 9097 |
rs190758224 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:176467 | TTGGTTTTAATTTTT[A/T]CTTTTTCTAGCTTAA | 9097 |
rs190779680 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP14 | GRCh38.p7 | 18:196292 | CAGGCTGAAGTGAGC[A/G]GATCATGAGGTCAGG | 9097 |
rs190960094 | snp | C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:181825 | GGTTACAAAGACTTA[C/G]TTCTTTGTTGTTTTT | 9097 |
rs190964972 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:165756 | AGTGATCTTAGGGGG[C/T]ATTTATAGTTATCAT | 9097 |
rs191018584 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:195146 | ACCTTTTTCTTTCAA[A/G]CTAATGAAATACTTT | 9097 |
rs191020277 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:200265 | CTACTGTTTTCTTAC[A/G/T]TGAAAATGAGAGTAA | 9097 |
rs191020521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:159513 | TGGTGTCTCCAATTG[A/G]CTGTAGGTGTGTGAT | 9097 |
rs191023837 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:164895 | AGTTAAGAATCCATC[C/G]CTGCCAGCATCATTG | 9097 |
rs191313362 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:187323 | TATGTGTTTGTATTA[G/T]GCCATTTTAACCATC | 9097 |
rs191394705 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:170887 | GGAGAGCATCAGGAT[A/T]AATAGCTAATGCATG | 9097 |
rs191396180 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:205752 | TGCCACAGCACTCCA[A/G]CCTGTATAACAAAGC | 9097 |
rs191481935 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:169931 | TTCTGACAGCCTCAC[C/T]GACCCGCAGTTCCCT | 9097 |
rs191534583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:193209 | GCGACGGGTTTTATC[A/G]TAATCCATGTATCAT | 9097 |
rs191541285 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:182430 | GCAGAAGAGAAGGGA[A/G]AGAAGGAGTGTGCAA | 9097 |
rs191550953 | snp | C/G | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212402 | ACTGGAGGTTGAGTT[C/G]GAGACCAGCCTGGCC | 9097 |
rs191562275 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:174022 | TCTTTTTTAAAGTTG[C/T]GTTGGCTATTCTGGG | 9097 |
rs191566847 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | USP14 | GRCh38.p7 | 18:204760 | GCTCAGCAATTACTC[A/T]GTCTTTTTTTTCCTG | 9097 |
rs191572282 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP14 | GRCh38.p7 | 18:208699 | TGTTGATTCTAGTTT[A/G]ATGCCATTGTGGTGA | 9097 |
rs191786914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:171655 | ACTATTCTGCAGCCC[A/G]TGGATCAGTAATTTC | 9097 |
rs191791660 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:197059 | GCAGTCCTAAATCCT[C/T]TAGCCCCTGGCTTTC | 9097 |
rs191816989 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP14 | GRCh38.p7 | 18:169466 | AGTGTTTTTTCTGTT[C/T]GTTAAAATGATGGTG | 9097 |
rs191817115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:190886 | TAATGGATGGTTTTA[C/T]ATGAATTAGGAATTA | 9097 |
rs191819923 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:165922 | TCTATAAAAGGGAGT[A/T]ATATAGAATCGACTT | 9097 |
rs191823113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:177932 | AGAATTTAATGCTCT[A/G]AAAATATTTGTATTT | 9097 |
rs192044812 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP14 | GRCh38.p7 | 18:173324 | CACCATGTTAGCCAG[A/G]ATGGTCTCTATCTCC | 9097 |
rs192078862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:191641 | TTGCACATTCTGAAA[C/T]GTAAAATAAACGGAA | 9097 |
rs192096409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:186524 | TTGGGAGGCTGAGGC[A/G]GGCAGATCACCGAAG | 9097 |
rs192132502 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:192160 | AGGTGTATGATTTTT[A/G]ATTGAATGTTTTTGA | 9097 |
rs192364491 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:178524 | TTGATGACTTTGGGC[A/G]ATTCTATATTGTCAT | 9097 |
rs192410900 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | USP14 | GRCh38.p7 | 18:210118 | CATATTTACTTATTC[G/T]GATGTGCTTTTCAAA | 9097 |
rs192414023 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | USP14 | GRCh38.p7 | 18:198661 | TTTATTTCTTGAAGG[A/T]TATTTATTATTTTTT | 9097 |
rs192454196 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | USP14 | GRCh38.p7 | 18:173267 | TGCCTGCCACCACAC[C/T]CGGCTATTTTTTTTG | 9097 |
rs192533949 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | USP14 | GRCh38.p7 | 18:166515 | TTTTTGTATTTTTAG[A/T]AGAGATGGAGTTTCT | 9097 |
rs192596972 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | USP14 | GRCh38.p7 | 18:184058 | TTGGAAAGAGTTCTG[G/T]GTAAGCAGGGGAGAT | 9097 |
rs192606357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:167266 | CAGCCTGGCAACAGA[A/G]CGAGACTCCGTCTCC | 9097 |
rs192607765 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP14 | GRCh38.p7 | 18:201630 | CCAGGAGCCAAATCA[C/T]GTAAGGCATGGTGTG | 9097 |
rs192623376 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP14 | GRCh38.p7 | 18:201482 | GGAAGGGTTGTTAAA[A/G]GGCATAAGAAGAAGA | 9097 |
rs192656408 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:200898 | CCTCTGACTCCCAGG[C/T]TCAAGAGATTCTCCT | 9097 |
rs192683440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:162049 | TAACCAGAATCATCC[A/G]TGTTGCAGCATGTAT | 9097 |
rs192723185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:197498 | GTATGTCTTATTTGG[C/T]TTAATATTTTTAAAG | 9097 |
rs192761729 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | USP14 | GRCh38.p7 | 18:188967 | TACAGGCGTGAGCCA[C/T]CGTGCTTGGCCTTTG | 9097 |
rs192768053 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:161453 | TGAGATTCAAAATTG[A/G]TAGTGATAACTCAGA | 9097 |
rs192854706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:183097 | TGCCTGGTGAATCTT[A/G]CTGTGTCTTTTATAT | 9097 |
rs192862814 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157256 | AATGAAATCTGCCAC[A/G]TCGATTGACTCTTCC | 9097 |
rs192918555 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:210864 | ATTATCATACATTAT[G/T]TAGCCTCTGGAAAAT | 9097 |
rs192926628 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:185095 | CTGGCAAGCCCCAGC[C/T]CTCAATATACACAGC | 9097 |
rs193001656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:207190 | ATGTCTGTCCTGATG[C/T]TCATACCAGACTGAC | 9097 |
rs193033316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:206309 | CTAGTGGCTGATGAA[A/G]TTGAGCATGTCTTCA | 9097 |
rs193050015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:171377 | TTGAAACCAATGCTC[A/G]TTTACCATTCCAAAA | 9097 |
rs193164759 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:202478 | GATTGGCTTTTATGC[A/G]TAAAACGTAAAGAAC | 9097 |
rs193166008 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:167718 | TGGGGGTGTCACTAT[A/G]TTGCCCAGGCTGGTC | 9097 |
rs199535772 | in-del | -/TT | | | intron-variant | USP14 | GRCh38.p7 | 18:180212 | TTAATGATTTAATCC[-/TT]TTTTTTTTTTTTTTC | 9097 |
rs199544050 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:184737 | TGTGCCACTGCACTC[C/T]AGGCTGGGTAATAGA | 9097 |
rs199593256 | in-del | -/C | 0.0908922 | 0.192833 | intron-variant | USP14 | GRCh38.p7 | 18:199770 | TAAGGTGTCCTTAAA[-/C]CAGAAACACACATAA | 9097 |
rs199629513 | snp | C/T | | | missense | USP14 | GRCh38.p7 | 18:198069 | CCTCATCTGCATCGG[C/T]AGCGACACCTTCTAA | 9097 |
rs199643514 | snp | C/T | 1.69769e-05 | 0.00291345 | intron-variant | USP14 | GRCh38.p7 | 18:211128 | TTCTTGTCCCTGTTA[C/T]TTAGATGAATGGATT | 9097 |
rs199693862 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:172569 | AGGAAGTCAGTCAGC[A/G]TGGCAGGTTTCATTG | 9097 |
rs199707354 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:184215 | TTTTTTGTACAGCAA[C/G]CTCTGATGCCAAACA | 9097 |
rs199730789 | snp | C/T | 0.000169107 | 0.00919375 | intron-variant | USP14 | GRCh38.p7 | 18:197728 | TGTGATTATAGACTT[C/T]CGTTATACCTTGATT | 9097 |
rs199771859 | snp | A/G | 0.000873816 | 0.0208841 | intron-variant | USP14 | GRCh38.p7 | 18:196777 | CAACAGGTAATTAGG[A/G]CAAGGTATTTTTCAT | 9097 |
rs199800690 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:192703 | TGCAAGACCAGAAGA[A/G]AAGAAAAGGAAAGGT | 9097 |
rs199876476 | in-del | -/GTTTTGCATGT | 0.00438332 | 0.0466095 | intron-variant | USP14 | GRCh38.p7 | 18:204882 | GTGCAGATCTTTAAA[-/GTTTTGCATGT]GTTTTATTTTCCTTT | 9097 |
rs199896795 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:203039 | TTTTTACCACCAAAT[A/G]ATTAAAACTTGTATG | 9097 |
rs199948389 | in-del | -/AAT | 0.00438332 | 0.0466095 | intron-variant | USP14 | GRCh38.p7 | 18:168353 | AACGTGTTATCTGCA[-/AAT]AATGACAATTTTACT | 9097 |
rs199949125 | snp | C/G/T | 0.0013962 | 0.0263892 | missense | USP14 | GRCh38.p7 | 18:198072 | CATCTGCATCGGCAG[C/G/T]GACACCTTCTAAAAA | 9097 |
rs200053399 | snp | A/G/T | 9.93499e-05 | 0.00704742 | intron-variant | USP14 | GRCh38.p7 | 18:202979 | TCGAAGCCAAATTCC[A/G/T]CTTCACTGAAATATT | 9097 |
rs200067358 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:189429 | CTGTTCAAATGTTGA[G/T]AAAAGCCACTAGAAA | 9097 |
rs200069635 | in-del | -/AAAT | | | intron-variant | USP14 | GRCh38.p7 | 18:170314 | GTCTCAAAAATAAAC[-/AAAT]AAATAAATAAATAAA | 9097 |
rs200086346 | in-del | -/AC | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212558 | GAGCTGAGATCACAC[-/AC]CACTGCACTCCAGCC | 9097 |
rs200087025 | in-del | -/AA | 0.030665 | 0.119967 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213150 | TGCTTGTAACTTTGC[-/AA]AAAGTCTTTTTTATT | 9097 |
rs200108555 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP14 | GRCh38.p7 | 18:185177 | TTATTTATTTATTTT[C/T]GAGACAGAGTCTCAC | 9097 |
rs200121257 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:169657 | ACACCTCATTTTATT[G/T]TGCTTCACAGATAAT | 9097 |
rs200198737 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:178889 | TTGACATAAACATTA[A/C]CAACTTTTAAGGATT | 9097 |
rs200235330 | in-del | -/TC | | | intron-variant | USP14 | GRCh38.p7 | 18:188525 | TTTTTTTTTTTTTTT[-/TC]CTTTGTGAGGGTTTG | 9097 |
rs200247406 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157930 | ATATATATATATATA[A/T]ATATATATAAATATA | 9097 |
rs200258698 | in-del | -/AAT | | | intron-variant | USP14 | GRCh38.p7 | 18:192260 | TGTTGTTTCACAATA[-/AAT]CTTTCAGAAAATGTT | 9097 |
rs200350859 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP14 | GRCh38.p7 | 18:191191 | TCTTAACAGGGAAAT[A/G]TAATGATTTTCAGGT | 9097 |
rs200390939 | in-del | -/TAGA | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:213976 | ACAAGATAGATAGAT[-/TAGA]TAGATAGATAGATAG | 9097 |
rs200401864 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:156810 | AAGGCTGGGTGCAGT[A/G]GCTTATGCCTGTAAT | 9097 |
rs200432904 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:182228 | GCCCTTTCTTCCGGT[A/G]AGTATAAGTGTAACT | 9097 |
rs200450700 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP14 | GRCh38.p7 | 18:176958 | GCTATTATCCTGGGT[A/G]TAAATTTGCTGCATG | 9097 |
rs200503546 | in-del | -/GT | 0.0659589 | 0.169201 | intron-variant | USP14 | GRCh38.p7 | 18:201384 | TTGATAAACACTGAA[-/GT]GTGGGACATGGATTA | 9097 |
rs200559280 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:210382 | GATTTACATCTTTCT[G/T]TAGATATTGGCTCCA | 9097 |
rs200586446 | in-del | -/T | 0.0134861 | 0.0810011 | intron-variant | USP14 | GRCh38.p7 | 18:209772 | TGTACTGTAACAAGA[-/T]TTTTATATTGTTGAA | 9097 |
rs200599951 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:205500 | GAAAGTTGGCCAGGC[A/C]TGGTGGCTCACGCTA | 9097 |
rs200624478 | snp | C/G | 0.000136916 | 0.0082728 | missense | USP14 | GRCh38.p7 | 18:163340 | AAGGAGAAATTTGAA[C/G]GTGTAGAATTGAATA | 9097 |
rs200736025 | in-del | -/CT | 0.00438332 | 0.0466095 | intron-variant | USP14 | GRCh38.p7 | 18:204757 | AGTGCTCAGCAATTA[-/CT]CTGTCTTTTTTTTCC | 9097 |
rs200757845 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | USP14 | GRCh38.p7 | 18:173256 | GGGACTACAGGTGCC[C/T]GCCACCACACCCGGC | 9097 |
rs200800220 | snp | A/G | 3.30224e-05 | 0.00406326 | missense | USP14 | GRCh38.p7 | 18:197645 | TTGGATACAAATGAT[A/G]CGAGTATTGCAACAG | 9097 |
rs200851217 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:207245 | GGCTTGAAATTGTGA[A/G]GTATCAGCCTTCACT | 9097 |
rs200879840 | in-del | -/TAAT | 0.0228947 | 0.104514 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213333 | GAATTTTAAAAATTG[-/TAAT]TAATTAATTCCTTAT | 9097 |
rs200890126 | snp | C/T | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213355 | ATTCCTTATCATCAT[C/T]ATAAAAAGCTTGATT | 9097 |
rs200939759 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:164765 | AGCCCCCTTTTTTCT[A/G]AACAGTAATTGTTAC | 9097 |
rs200942846 | in-del | -/TTTATTTTATTTTATTTTTA | 0.00438332 | 0.0466095 | intron-variant | USP14 | GRCh38.p7 | 18:208087 | GTTTTATTTGTTTAT[-/TTTATTTTATTTTATTTTTA]TTTATTTTTTTTCTA | 9097 |
rs200975159 | in-del | -/ATATATAA | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157933 | TATATATATATAAAT[-/ATATATAA]ATATATAAATATATA | 9097 |
rs200989362 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:190925 | GCTCTAATATGGGAA[-/T]TTTTTTTTTGGATAT | 9097 |
rs201009137 | in-del | -/A | | | intron-variant | USP14 | GRCh38.p7 | 18:199547 | TAGAACTGTTGTTTT[-/A]AAAAAAAAATTTCTG | 9097 |
rs201025233 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:156658 | CATTTTACATGCACA[A/G]CTTGAACACATTGCT | 9097 |
rs201066808 | snp | G/T | 0.00199794 | 0.0315432 | intron-variant | USP14 | GRCh38.p7 | 18:211104 | AATCCTGCATAACAT[G/T]AATTCATCTTCTTGT | 9097 |
rs201080569 | snp | C/G/T | 0.000399281 | 0.0141238 | missense | USP14 | GRCh38.p7 | 18:163395 | AGGCTCAGCTGTTTG[C/G/T]GTTGACTGGAGTCCA | 9097 |
rs201094792 | in-del | -/GAG | 0.0364509 | 0.129988 | cds-indel | USP14 | GRCh38.p7 | 18:212505 | GCTACTTGGGAGGCT[-/GAG]GTGGGAGAATTGCTT | 9097 |
rs201096026 | in-del | -/A | 0.210301 | 0.246828 | intron-variant | USP14 | GRCh38.p7 | 18:168860 | GTGGATCACGAAGTC[-/A]GGAGATCGAGACCAT | 9097 |
rs201162022 | snp | A/T | 1.65222e-05 | 0.00287417 | intron-variant | USP14 | GRCh38.p7 | 18:198152 | CCTTATGAGCCAAGA[A/T]ATAGACTATACTCAT | 9097 |
rs201164829 | snp | A/T | 0.00199806 | 0.0315443 | missense | USP14 | GRCh38.p7 | 18:204670 | ATCTAGAAGATAAAA[A/T]AGTGAATCAGCAGCC | 9097 |
rs201167227 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:203670 | GCTGGAGTGCAGTGG[C/T]GCTATCTTGGCTCAC | 9097 |
rs201237605 | snp | C/T | 0.00113983 | 0.0238456 | synonymous-codon | USP14 | GRCh38.p7 | 18:180254 | GAGTTACCATGTGGA[C/T]TGACAAACCTTGGTA | 9097 |
rs201332664 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:173123 | TTTTTTTTTTTTTTT[C/T]TTTGAGACGGAGTCT | 9097 |
rs201342983 | in-del | -/A | | | intron-variant | USP14 | GRCh38.p7 | 18:205781 | CAAGACTCTGTTTCT[-/A]AAAAAAAAATTATAC | 9097 |
rs201376847 | in-del | -/G | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:156737 | TCACACAAAGTTTTT[-/G]GTTTTCCCAGTGCAT | 9097 |
rs201404886 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:162353 | CACATCTTTGCTAAC[A/G]CTTGTTATTTTCTGT | 9097 |
rs201406393 | snp | C/G/T | 1.65097e-05 | 0.00287308 | intron-variant | USP14 | GRCh38.p7 | 18:166770 | GGTTAAATGTCTTTT[C/G/T]TTTGTCTTTGAAACA | 9097 |
rs201481755 | snp | C/T | 0.000256855 | 0.0113297 | intron-variant | USP14 | GRCh38.p7 | 18:204524 | AAATAAATATCTTTA[C/T]AAATGTGTTTACACA | 9097 |
rs201500120 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:182259 | TAAAAAATATGTAAC[C/T]TAATTCTGACTAAAT | 9097 |
rs201506930 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:195385 | TGCTAAGATGCTGTA[G/T]TTGGTGGGTTCAGTC | 9097 |
rs201621352 | in-del | -/AT | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157995 | TATAAAAATATATAA[-/AT]ATATATATATAGAAC | 9097 |
rs201647105 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:197752 | TTGATTTTTTTTTTT[-/T]ATTTTTTTTCCCCTC | 9097 |
rs201651146 | in-del | -/CA | 0.0737376 | 0.17729 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212557 | GCAGTGAGCTGAGAT[-/CA]CACACCACTGCACTC | 9097 |
rs201652385 | snp | A/G | 6.61759e-05 | 0.00575183 | intron-variant | USP14 | GRCh38.p7 | 18:203068 | TGGTATTTTGATGTA[A/G]TGGGATTTCTTTACA | 9097 |
rs201773333 | snp | A/T | 0.000544829 | 0.016496 | intron-variant | USP14 | GRCh38.p7 | 18:204731 | TACTCTTAATATCTT[A/T]ATCTCCCATCAGTGC | 9097 |
rs201785469 | snp | A/G | 0.000144368 | 0.00849489 | intron-variant | USP14 | GRCh38.p7 | 18:179045 | CATCTGCTGTAAGAC[A/G]CACCAGATTTTATGT | 9097 |
rs201860813 | snp | A/G | | | missense | USP14 | GRCh38.p7 | 18:199291 | TCAATCAGGAAGTCA[A/G]GTATCTTTTTACAGG | 9097 |
rs201863478 | in-del | -/TA | 0.220246 | 0.248223 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213122 | TTATAATGATTCATG[-/TA]TATATTTGTATGATG | 9097 |
rs201867535 | in-del | -/GTTA | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:214123 | TTAGTTAGTTAGTTA[-/GTTA]TGAGTGAGCACAGCT | 9097 |
rs201975297 | snp | C/T | 3.30589e-05 | 0.00406551 | missense | USP14 | GRCh38.p7 | 18:163367 | AATACAGATGAACCT[C/T]CAATGGTATTCAAGG | 9097 |
rs201983733 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP14 | GRCh38.p7 | 18:170317 | TCAAAAATAAACAAA[C/T]AAATAAATAAATAAA | 9097 |
rs202058126 | snp | C/G | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:211908 | TTTATTATTGTGTCT[C/G]TCTCTGATGTACTGT | 9097 |
rs202151884 | in-del | -/T | | | intron-variant | USP14 | GRCh38.p7 | 18:173240 | GCCTCCCGAGTAGCT[-/T]GGGACTACAGGTGCC | 9097 |
rs202190126 | in-del | -/GACAAA | 0.031825 | 0.122064 | intron-variant | USP14 | GRCh38.p7 | 18:186043 | TTTCAACTTGTTCTT[-/GACAAA]AAAATTTTAAATAAC | 9097 |
rs202201124 | in-del | -/TGTT | | | intron-variant | USP14 | GRCh38.p7 | 18:178004 | GTTTGTTTGTTTGTT[-/TGTT]ATATTTTTTGAGACG | 9097 |
rs202224437 | in-del | -/A | 0.0142736 | 0.0832652 | intron-variant | USP14 | GRCh38.p7 | 18:208110 | ATTTTATTTTTATTT[-/A]TTTTTTTTCTATTGC | 9097 |
rs367551785 | snp | A/T | 0.000298018 | 0.0122033 | missense | USP14 | GRCh38.p7 | 18:211262 | GCAGAGTTGAAATAA[A/T]GGAAGAGGAAAGTGA | 9097 |
rs367638267 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:184353 | CTGATAAAACAAGAA[G/T]GAAAGAACAGAAAAA | 9097 |
rs367641754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:159484 | CTTATTCAAAATGGC[A/G]CCTAAAATATGTGTG | 9097 |
rs367681523 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:159415 | TTGCTGACAGTCCAG[G/T]GTACTGGCCAGGGAT | 9097 |
rs367731566 | in-del | -/TA | | | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:213297 | AGAGCAAAGTATATA[-/TA]AGCCTTGTATGGACT | 9097 |
rs367749117 | in-del | -/TATATA | | | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157912 | CACAAACCTTCAATT[-/TATATA]TATATATATATAAAT | 9097 |
rs367784404 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:162946 | GGGATTACAGGCGTG[C/T]GCCACCACACCTGGC | 9097 |
rs367897326 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:180774 | TTCCTATTTTATGGC[C/T]GAATAGTATTTCATG | 9097 |
rs367934425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:170028 | CCCTACAGGCTGAGC[A/G]CGGTGGCTCACACCT | 9097 |
rs367938622 | snp | A/C/G | | | intron-variant | USP14 | GRCh38.p7 | 18:208485 | TAGTTGTATTGATTT[A/C/G]TGCTCTTATTTCCTT | 9097 |
rs367952971 | in-del | -/GC | | | intron-variant | USP14 | GRCh38.p7 | 18:179585 | ATGGTTTTTTTTTTT[-/GC]TTTTTTTTTTTTTTT | 9097 |
rs368034676 | snp | A/G | 1.65192e-05 | 0.00287391 | intron-variant | USP14 | GRCh38.p7 | 18:192791 | TTTCTTCCCATTTGA[A/G]TGTTAGAATGAATTG | 9097 |
rs368047770 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP14 | GRCh38.p7 | 18:173569 | GGCATGCACCACCAC[A/G]CCCAGCTAATTGTTT | 9097 |
rs368062061 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:174931 | CAGGAATGTGCCACC[A/G]CGCCGGACTAATTTT | 9097 |
rs368077279 | snp | C/T | 0.00168699 | 0.0289939 | intron-variant | USP14 | GRCh38.p7 | 18:163305 | TTGTGATTTTGTTTG[C/T]AGTTACTGTAAAATG | 9097 |
rs368168636 | in-del | -/G | | | intron-variant | USP14 | GRCh38.p7 | 18:189491 | GTTTGTTTTTTCTTT[-/G]TTTTTTTTTTGAGAA | 9097 |
rs368225233 | snp | A/T | 0.000104681 | 0.00723392 | intron-variant | USP14 | GRCh38.p7 | 18:202840 | GCAGAAATAAAATTT[A/T]TAAAACTAATGTTTG | 9097 |
rs368237068 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:170603 | CCTTATTGCTGATAT[A/G]GAGTAAGTTTAAGTG | 9097 |
rs368355459 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:197264 | AAAGCCTTAGGCTTT[C/T]CCTGATGACCTTATT | 9097 |
rs368435996 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:176821 | GTATGAAGTAGAGAG[C/T]TGATAGTATGTTTTT | 9097 |
rs368446406 | snp | A/G | 5.11775e-05 | 0.00505827 | intron-variant, missense | USP14 | GRCh38.p7 | 18:179018 | TAGAAGACATGACAG[A/G]AGAACAGTTAGCATC | 9097 |
rs368468063 | snp | A/G | 3.30251e-05 | 0.00406343 | intron-variant | USP14 | GRCh38.p7 | 18:166763 | CAGTGGTGGTTAAAT[A/G]TCTTTTGTTTGTCTT | 9097 |
rs368503047 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:166738 | ATTATTAGATTGTGT[C/T]CAGCTTGTACAGTGG | 9097 |
rs368517080 | in-del | -/T | 0.226779 | 0.248919 | intron-variant | USP14 | GRCh38.p7 | 18:185143 | GCTGATTTTCTTTCA[-/T]TTTTTTTTTTCTTAT | 9097 |
rs368569062 | snp | A/G | | | downstream-variant-500B | USP14, THOC1 | GRCh38.p7 | 18:213974 | GGACAAGATAGATAG[A/G]TTAGATAGATAGATA | 9097 |
rs368601925 | snp | C/T | 0.000616636 | 0.0175482 | intron-variant | USP14 | GRCh38.p7 | 18:203205 | GGTTAGTAATGAACT[C/T]TACTTTGTATAAGAA | 9097 |
rs368615666 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:166863 | TAATGCAGTAACCTC[A/G]TTATGATACCAAAAT | 9097 |
rs368663005 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:193439 | CTCTCTAACAGCTTT[A/T]TTGATATAGTGTACA | 9097 |
rs368682455 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP14 | GRCh38.p7 | 18:179733 | GCGAAAATTGTAGGC[A/G]TGCACCATCATGCCC | 9097 |
rs368695998 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:164435 | TTTATTGCATCCTAC[A/C]CATTAACGAAGAGCT | 9097 |
rs368707018 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:193613 | TCCCATTTCTAGCCC[C/T]ACCCATTTATCTATG | 9097 |
rs368708925 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:163809 | CTAAGCATAGTACCC[A/G]ATAGGTAGTTTTTTT | 9097 |
rs368715697 | snp | C/T | 0.000307953 | 0.0124049 | intron-variant | USP14 | GRCh38.p7 | 18:197595 | CCAGGATTACTTACT[C/T]TGTCTTTTTTTACAT | 9097 |
rs368794249 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:187127 | AACTACTGTTTACTC[A/G]TGAGTTTATTGGTGA | 9097 |
rs368830212 | in-del | -/T | 0.000479885 | 0.0154826 | intron-variant | USP14 | GRCh38.p7 | 18:166828 | AAAAATGTAAGTATT[-/T]ATCTTATGAACGTTT | 9097 |
rs368895827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP14 | GRCh38.p7 | 18:198574 | AGGAATTTGGAAAAA[C/T]ATACCTATTGGAGTG | 9097 |