SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs11801 | snp | A/G | 0.450483 | 0.149354 | intron-variant | USP7 | GRCh38.p7 | 16:8896382 | GTGAGACCCTAATCT[A/G]TTACCTAATAAGAGT | 7874 |
rs30761 | snp | A/T | 0.0256215 | 0.110247 | intron-variant | USP7 | GRCh38.p7 | 16:8921395 | AAATTCCCATTTATG[A/T]TTTCATTGCTCTCTC | 7874 |
rs30762 | snp | A/T | 0.0980852 | 0.198549 | intron-variant | USP7 | GRCh38.p7 | 16:8922359 | TGGGTGTGGTGGCAC[A/T]CGCCTATAGTCCCAG | 7874 |
rs30763 | snp | C/T | 0.421051 | 0.182323 | intron-variant | USP7 | GRCh38.p7 | 16:8922767 | ACATTTCATAATATA[C/T]ATGAATGTTTAAATG | 7874 |
rs30764 | snp | A/G | 0.409212 | 0.192748 | intron-variant | USP7 | GRCh38.p7 | 16:8954495 | TAACAGGGTAATCCT[A/G]AAATCTCACAAGCTG | 7874 |
rs39863 | snp | A/T | 0.0926964 | 0.194308 | intron-variant | USP7 | GRCh38.p7 | 16:8921902 | TTAAGGTTTGCGATT[A/T]AAGTGGGGCCTTATC | 7874 |
rs39864 | snp | G/T | 0.137867 | 0.223442 | intron-variant | USP7 | GRCh38.p7 | 16:8952115 | AAAAAAATGGCCAGG[G/T]GTGGTGTGCCTGTAG | 7874 |
rs42554 | snp | C/G | 0.0295553 | 0.11824 | intron-variant | USP7 | GRCh38.p7 | 16:8921071 | ATCTGACTCTAAAAT[C/G]AATAAAGGACTTGAA | 7874 |
rs166231 | snp | C/T | 0.449599 | 0.150533 | intron-variant | USP7 | GRCh38.p7 | 16:8939733 | GAAGGAAAACACATA[C/T]ACTATTCACATTACG | 7874 |
rs166232 | snp | C/T | 0.445987 | 0.155207 | intron-variant | USP7 | GRCh38.p7 | 16:8941527 | GACATGTCCAGTAAC[C/T]TGTCCTAAGCCAAAA | 7874 |
rs173863 | snp | A/G | 0.0998734 | 0.199905 | intron-variant | USP7 | GRCh38.p7 | 16:8948652 | ggaatattattctgc[A/G]agaaaagggaacgac | 7874 |
rs173864 | snp | G/T | 0.0232847 | 0.105357 | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891662 | TGCAACGTGGGTGCC[G/T]TGACAGGGCGAGAAG | 7874 |
rs183725 | snp | A/G | 0.341685 | 0.232581 | intron-variant | USP7 | GRCh38.p7 | 16:8954178 | TCTGCCTCCAGTGGC[A/G]CCGCAGGGGGCACGT | 7874 |
rs187614 | snp | C/T | 0.432357 | 0.171014 | intron-variant | USP7 | GRCh38.p7 | 16:8939020 | atacccttttcctag[C/T]ttccccttacagcac | 7874 |
rs254943 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | USP7 | GRCh38.p7 | 16:8940566 | TGGCCCCTGCATCAG[A/G]AAGGGAGAGGTGGGA | 7874 |
rs254944 | snp | C/T | 0.030278 | 0.119257 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950009 | CTGTCCCACCAACCA[C/T]AGAAGCCAGGAGCTG | 7874 |
rs876884 | snp | C/T | 0.357451 | 0.225731 | intron-variant | USP7 | GRCh38.p7 | 16:8902931 | ATTCTAATTCTTCCC[C/T]GGTTGATTTGGACAA | 7874 |
rs899253 | snp | A/C | 0.436265 | 0.166749 | intron-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894278 | CCCACACCCTGACTG[A/C]GCCTCAGAGCCACTG | 7874 |
rs899254 | snp | A/G | 0.459687 | 0.136129 | intron-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894331 | TCACCCTGCACACAT[A/G]TCCAAGCTTCTCTCC | 7874 |
rs960733 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8952471 | cccctagaacctcca[A/G]aaggagtgtggccct | 7874 |
rs960734 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | USP7 | GRCh38.p7 | 16:8952465 | GAACCTCCAGAAGGA[A/G]TGTGGCCCTGCTGGC | 7874 |
rs1050394 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893721 | CGCAATGGGGGAGAA[A/G]AGGTTAGTGGATCGG | 7874 |
rs1058329 | snp | C/G | 0.194902 | 0.243853 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962683 | CTGCGTTCCTTGCAG[C/G]TATTTTCGAACGTAA | 7874 |
rs1347580 | snp | C/T | 0.4231 | 0.180378 | intron-variant | USP7 | GRCh38.p7 | 16:8905691 | GCCATACTGAGCACA[C/T]CAAACGAGAGTTCAA | 7874 |
rs1382390 | snp | C/G | 0.0127356 | 0.0788577 | synonymous-codon, utr-variant-5-prime, intron-variant | USP7 | GRCh38.p7 | 16:8936587 | CCACAGGCTTGGGCT[C/G]GAAGGTGAGTCAGGT | 7874 |
rs1471435 | snp | C/T | 0.44755 | 0.153212 | intron-variant | USP7 | GRCh38.p7 | 16:8941267 | TGGAAAAATTAACTA[C/T]GCTCAAACATAACCC | 7874 |
rs1529916 | snp | C/T | 0.396364 | 0.202676 | intron-variant | USP7 | GRCh38.p7 | 16:8897333 | ACAGGCTTCTTGCAT[C/T]AAGGCCACTTTTGTT | 7874 |
rs1542540 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | USP7 | GRCh38.p7 | 16:8932322 | tataatcctagcact[C/T]tgggaggcaaagatg | 7874 |
rs1542541 | snp | A/G | 0.386884 | 0.209196 | intron-variant | USP7 | GRCh38.p7 | 16:8932543 | TCAAGACACAGGATG[A/G]AGAGAAGGAAAAATG | 7874 |
rs1600194 | snp | A/C | 0.0603597 | 0.1629 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964602 | AAACAAAACCCAAAA[A/C]CTTTGTAGAGAGGGT | 7874 |
rs1622768 | snp | C/G | 0.404559 | 0.196498 | intron-variant | USP7 | GRCh38.p7 | 16:8936339 | TTGAACTCCCTCTGG[C/G]TTCTGCATGGTCCTC | 7874 |
rs1657066 | snp | A/C | 0.408871 | 0.193029 | intron-variant | USP7 | GRCh38.p7 | 16:8906228 | TTACTCACAAAGAGA[A/C]GCACAAATGCTAATT | 7874 |
rs1657076 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | USP7 | GRCh38.p7 | 16:8896648 | AACAGAGGAAGGATA[C/T]GATTCCATTTGAACG | 7874 |
rs1657077 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | USP7 | GRCh38.p7 | 16:8896363 | CCTAATAAGAGTAAG[C/T]GAGGAAAACGCCACT | 7874 |
rs1657084 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | USP7 | GRCh38.p7 | 16:8925295 | TAACACACACAAAAC[A/G]CAGGCCTCAACAAAA | 7874 |
rs1657086 | snp | C/G | 0.403334 | 0.197456 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937059 | TAAAAAGGCAAAGTA[C/G]AATGCCCTCTCAGCC | 7874 |
rs1657087 | snp | A/C/G | 0.375 | 0.216506 | intron-variant | USP7 | GRCh38.p7 | 16:8953704 | GAAGACACGTGCCCC[A/C/G]TGCGGCGCCACCGGA | 7874 |
rs1657088 | snp | C/T | 0.367091 | 0.220884 | intron-variant | USP7 | GRCh38.p7 | 16:8953716 | CCCGTGCGGCGCCAC[C/T]GGAGGCAGAGGGAAG | 7874 |
rs1657091 | snp | C/T | 0.415563 | 0.18732 | intron-variant | USP7 | GRCh38.p7 | 16:8901557 | GGAAGAGCGTTGCCA[C/T]GGGAAGATTGCGCAT | 7874 |
rs1677468 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | USP7 | GRCh38.p7 | 16:8935752 | CCTACTTGGTGTTTC[A/G]AAAACATATTTTCTG | 7874 |
rs1677470 | snp | C/T | 0.00760928 | 0.0612106 | intron-variant | USP7 | GRCh38.p7 | 16:8920493 | GAATAAGAACACACA[C/T]TTTATTCCCAAGAGA | 7874 |
rs1677472 | snp | C/T | 0.0260105 | 0.111035 | intron-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894381 | CAAAGGATGTAAGGA[C/T]CTGTTAAGAACTCGT | 7874 |
rs1677473 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | USP7 | GRCh38.p7 | 16:8895546 | TGGTATAAAAACACA[A/G]ATCAAGCTACTTGTA | 7874 |
rs1677480 | snp | G/T | 0.435263 | 0.167862 | intron-variant | USP7 | GRCh38.p7 | 16:8933584 | GTAGTTTCTTCACTG[G/T]ATATGCACACACTCA | 7874 |
rs1677490 | snp | C/G | 0.426354 | 0.177198 | intron-variant | USP7 | GRCh38.p7 | 16:8934684 | GATTGGCCACACCAA[C/G]TCAGATGTGTTAATT | 7874 |
rs1677491 | snp | G/T | 0.441705 | 0.160466 | intron-variant | USP7 | GRCh38.p7 | 16:8909393 | TGTACATCAGCTCAT[G/T]TAAGAGGACAGAGCT | 7874 |
rs1816548 | snp | G/T | 0.00479614 | 0.0487346 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893915 | TGCACGTGCCCTCTA[G/T]CCGAAGTCTTCAGCA | 7874 |
rs1865807 | snp | G/T | 0.0558544 | 0.157504 | intron-variant | USP7 | GRCh38.p7 | 16:8948554 | AAATCCCTTTAAAAA[G/T]ACTGACTAAAGCCTA | 7874 |
rs1871210 | snp | A/G | 0.0995161 | 0.199636 | intron-variant | USP7 | GRCh38.p7 | 16:8948744 | aGCATGGACAACACA[A/G]CGATAAAAGCAGCCA | 7874 |
rs1972295 | snp | G/T | 0.0562307 | 0.157967 | intron-variant | USP7 | GRCh38.p7 | 16:8927707 | caggcgtggtggcat[G/T]tgcctgtaatcccag | 7874 |
rs2086154 | snp | A/C | 0.392696 | 0.205275 | intron-variant | USP7 | GRCh38.p7 | 16:8948774 | AAAAACAAGCATGGA[A/C]AACACAGCGAAACCC | 7874 |
rs2126999 | snp | C/T | 0.0477023 | 0.146886 | intron-variant | USP7 | GRCh38.p7 | 16:8919607 | ACTCCCAGAGCTTTT[C/T]TTATTTTGTGATTTT | 7874 |
rs2164506 | snp | A/G | 0.0928121 | 0.194402 | intron-variant | USP7 | GRCh38.p7 | 16:8919178 | GGGGATCTTGCAGAT[A/G]CCCCATTGCTCCTGC | 7874 |
rs2164507 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | USP7 | GRCh38.p7 | 16:8919839 | GGAGACACCTACTGC[A/G]CAGTACCATTCACCA | 7874 |
rs2217910 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | USP7 | GRCh38.p7 | 16:8909348 | ACTGGGGACCATGAC[A/G]AGGCACACCCATATG | 7874 |
rs2248797 | snp | C/T | 0.445724 | 0.155538 | intron-variant | USP7 | GRCh38.p7 | 16:8946462 | CTCCAGAAAGACTTA[C/T]GCTCCAGAAAGAAGC | 7874 |
rs2248802 | snp | A/G | 0.101301 | 0.200969 | intron-variant | USP7 | GRCh38.p7 | 16:8946690 | TCTGGTCACTGGCCT[A/G]TACCCCAGCCCCACA | 7874 |
rs2257181 | snp | G/T | 0.407845 | 0.193868 | intron-variant | USP7 | GRCh38.p7 | 16:8896823 | CTCAACACAGACCCA[G/T]TGTTGCTCCAGTTTT | 7874 |
rs2289109 | snp | A/C | 0.489893 | 0.0703642 | intron-variant | USP7 | GRCh38.p7 | 16:8898971 | TGTCACCACTCACAT[A/C]TTGACCACATTACTC | 7874 |
rs2289110 | snp | A/G | 0.0577344 | 0.159793 | intron-variant, missense | USP7 | GRCh38.p7 | 16:8894418 | GACCTGTGGAACCAG[A/G]AGCAATAGCATTCCA | 7874 |
rs2289111 | snp | A/G | 0.000115448 | 0.00759675 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8915520 | ATTTTCCACATTATC[A/G]AGCAACTGAAAAAGA | 7874 |
rs2304464 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | USP7 | GRCh38.p7 | 16:8898695 | TGCTCACTCACAGAT[A/G]TTTGTTTTTAGGCAA | 7874 |
rs2304465 | snp | C/T | 0.479029 | 0.100229 | intron-variant | USP7 | GRCh38.p7 | 16:8898485 | CATAAAGAGAAGGCT[C/T]GGGGTTTTGGTGACG | 7874 |
rs2304466 | snp | A/G | 0.5 | 0.00040385 | intron-variant | USP7 | GRCh38.p7 | 16:8902070 | GCAGGCAGGCGTCTC[A/G]TGGGCACTTACGATC | 7874 |
rs2304467 | snp | C/G | 0.438666 | 0.164028 | intron-variant | USP7 | GRCh38.p7 | 16:8894920 | TTGGTTTTGGCGGCT[C/G]CCACGTGACGTGGCC | 7874 |
rs2304473 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | USP7 | GRCh38.p7 | 16:8919251 | ACCGAGGCCAGGAAC[A/G]CTTATCACACAGCAT | 7874 |
rs2437711 | snp | C/T | 0.442655 | 0.159323 | intron-variant | USP7 | GRCh38.p7 | 16:8912328 | gtggtggtgggcacc[C/T]gtaatcccagctact | 7874 |
rs2437713 | snp | G/T | 0.132066 | 0.220435 | intron-variant | USP7 | GRCh38.p7 | 16:8926952 | ACGAAGTTCCCACTG[G/T]GCACTTTGTTACAGC | 7874 |
rs2437714 | snp | C/T | 0.0346268 | 0.126943 | intron-variant | USP7 | GRCh38.p7 | 16:8934124 | CTTGGTTCAAACTTA[C/T]CCTACGACAATAGCT | 7874 |
rs2437715 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | USP7 | GRCh38.p7 | 16:8934955 | ACATGGTAAATCCCT[A/G]GTCCAGAAGTAAATG | 7874 |
rs2437716 | snp | C/T | 0.143959 | 0.226396 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937247 | acgaaacaacgtgta[C/T]aagacaagcaatctg | 7874 |
rs2437717 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | USP7 | GRCh38.p7 | 16:8942676 | CCTCAAGCTCTTGAG[C/T]AGCTGGGACTACAGG | 7874 |
rs2437718 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | USP7 | GRCh38.p7 | 16:8942840 | GACATGAGCCACCAC[A/G]TCCAGCCACTTTGTG | 7874 |
rs2437719 | snp | C/G | 0.0352966 | 0.128072 | intron-variant | USP7 | GRCh38.p7 | 16:8944407 | CACCTTGGCAACTAA[C/G]TAGCAGCTTCCTCTC | 7874 |
rs2437724 | snp | A/C | 0.0236746 | 0.106192 | intron-variant | USP7 | GRCh38.p7 | 16:8899011 | CTAAGCAAGAAATGG[A/C]CTGTCAGGTGAAATG | 7874 |
rs2437725 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | USP7 | GRCh38.p7 | 16:8899012 | TAAGCAAGAAATGGA[A/C]TGTCAGGTGAAATGG | 7874 |
rs2437726 | snp | A/T | 0.455621 | 0.142197 | intron-variant | USP7 | GRCh38.p7 | 16:8900035 | GCACCTGCTCTCCTC[A/T]ACAGGAGCAGACCCA | 7874 |
rs2437727 | snp | C/G | 0.432082 | 0.197628 | intron-variant | USP7 | GRCh38.p7 | 16:8904714 | TTGGGAGGCTGAGGC[C/G]GGCCGATCACGAGGT | 7874 |
rs2447911 | snp | A/C | 0.442249 | 0.159814 | intron-variant | USP7 | GRCh38.p7 | 16:8924808 | CTCAAAGAAGGTAGA[A/C]GTGCTTACCGTCACA | 7874 |
rs2447912 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | USP7 | GRCh38.p7 | 16:8920577 | GTCTAAAATTAGCAA[A/C]AAAGTTGGGATGTAT | 7874 |
rs2447913 | snp | G/T | 0.119281 | 0.213102 | intron-variant | USP7 | GRCh38.p7 | 16:8916234 | ATTGGTATATATACA[G/T]GAGTTATTAATCCAG | 7874 |
rs2447914 | snp | C/T | 0.443464 | 0.15834 | intron-variant | USP7 | GRCh38.p7 | 16:8911783 | ttctcactgaCAGCT[C/T]CGGAAGAAACTGCAC | 7874 |
rs2447915 | snp | A/G | 0.45645 | 0.140991 | intron-variant | USP7 | GRCh38.p7 | 16:8911210 | GAGGTTTTCCTTGTC[A/G]TTCTGCCACATCAGC | 7874 |
rs2447916 | snp | G/T | 0.00745915 | 0.060613 | intron-variant | USP7 | GRCh38.p7 | 16:8910707 | GTGTCCTGTTGTAGC[G/T]TTCTTCTTTATTTTC | 7874 |
rs2447917 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | USP7 | GRCh38.p7 | 16:8906799 | TATATTTGGAATTCC[C/T]CCACCCTAAATTATT | 7874 |
rs2447918 | snp | A/G | 0.470724 | 0.117425 | intron-variant | USP7 | GRCh38.p7 | 16:8902520 | GACTAAAATATGAGC[A/G]TGTTTTTATTTTAAT | 7874 |
rs2447919 | snp | A/G | 0.386694 | 0.20932 | intron-variant | USP7 | GRCh38.p7 | 16:8900706 | AGAGAAAATACTTAA[A/G]TACATGGAAGACTAT | 7874 |
rs2447931 | snp | C/G | 0.372995 | 0.217652 | intron-variant | USP7 | GRCh38.p7 | 16:8942424 | TCAGACCCTCACAGT[C/G]CTGCAGAACAGCAAA | 7874 |
rs2447933 | snp | A/G | 0.442655 | 0.159323 | intron-variant | USP7 | GRCh38.p7 | 16:8934773 | TGTACTCGGTGGCCA[A/G]CCAGTGGCCCTTTGC | 7874 |
rs3214650 | in-del | -/C | 0.0407518 | 0.136803 | intron-variant, frameshift-variant | USP7 | GRCh38.p7 | 16:8894530 | GGGTTCTCCCCCCCC[-/C]GGGGGCTGGTGTGGG | 7874 |
rs3826203 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | USP7 | GRCh38.p7 | 16:8911174 | GTCTCAAAAGCAGAG[A/G]TGCACAAATGTGAAT | 7874 |
rs3841558 | in-del | -/TTTCTGAATTAGGTCT | | | intron-variant | USP7 | GRCh38.p7 | 16:8916405 | AACAAAGATGGGCAT[-/TTTCTGAATTAGGTCT]GAGGTTTTACTTGGT | 7874 |
rs4076904 | snp | A/C | 0.347032 | 0.230401 | intron-variant | USP7 | GRCh38.p7 | 16:8958616 | GATGTGGGATAGAGA[A/C]AGCAGAGTTCAAAGC | 7874 |
rs4539593 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | USP7 | GRCh38.p7 | 16:8931395 | GTTTCACCATGTCGG[C/T]CAACTGGTCTCGAAC | 7874 |
rs4985011 | snp | A/T | 0.45889 | 0.13735 | intron-variant | USP7 | GRCh38.p7 | 16:8902981 | ATCGAATGCCCATTT[A/T]CAAAAATAAAGAGGG | 7874 |
rs4985012 | snp | A/G | 0.494692 | 0.0512434 | intron-variant | USP7 | GRCh38.p7 | 16:8906146 | GGGTAATTATCCCAC[A/G]AGCATTCAGAAGAAA | 7874 |
rs4985013 | snp | A/G | 0.45574 | 0.142025 | intron-variant | USP7 | GRCh38.p7 | 16:8914618 | ctcatgaatgtgctg[A/G]gcaaaaggaatcaga | 7874 |
rs4985014 | snp | C/G | 0.0376037 | 0.131863 | intron-variant | USP7 | GRCh38.p7 | 16:8941448 | ACAGGAAGGACCTGA[C/G]GGGTAAAGGCACGTA | 7874 |
rs4985061 | snp | C/G | 0.487809 | 0.0771174 | intron-variant | USP7 | GRCh38.p7 | 16:8900335 | AATTTTTAAGAAATT[C/G]AGAAGAGCTTTATGA | 7874 |
rs4985062 | snp | C/T | 0.463018 | 0.130857 | intron-variant | USP7 | GRCh38.p7 | 16:8902779 | TGTAATCCCAGCTAC[C/T]TGGGAGGCTGAGGCA | 7874 |
rs4985063 | snp | A/G | 0.48955 | 0.071525 | intron-variant | USP7 | GRCh38.p7 | 16:8902894 | AAAAAAAGAAAAAAA[A/G]ACTGTGATTCTAAGA | 7874 |
rs4985065 | snp | A/C | 0.486855 | 0.0799975 | intron-variant | USP7 | GRCh38.p7 | 16:8908815 | GAACCACAGAAAAAT[A/C]ATTAAATGGAAAATC | 7874 |
rs4985073 | snp | G/T | 0.499539 | 0.0151687 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8965256 | GCTCAATAAAAATTG[G/T]TTGGGCCAGGTCGGC | 7874 |
rs6498252 | snp | A/G | 0.0382264 | 0.132861 | intron-variant | USP7 | GRCh38.p7 | 16:8919555 | CACAAGAAGAAACAG[A/G]AGTGTGTATTCACCA | 7874 |
rs6498271 | snp | C/G | 0.347032 | 0.230401 | intron-variant | USP7 | GRCh38.p7 | 16:8954472 | TCATGGGCAATGGGA[C/G]CACAATACAGCTTGT | 7874 |
rs7184566 | snp | A/T | 0.0256215 | 0.110247 | intron-variant | USP7 | GRCh38.p7 | 16:8930949 | ACTCCAGCCTGGCCG[A/T]CAGGGTGAGACTCAG | 7874 |
rs7189170 | snp | A/G | 0.488302 | 0.0755777 | intron-variant | USP7 | GRCh38.p7 | 16:8920528 | TTACATTAGTGCCCT[A/G]TACTTAATAGAGATG | 7874 |
rs7190551 | snp | A/G | 0.339429 | 0.233457 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938158 | TGAGCAAACAGGCAC[A/G]ACACTCCGAGAAGGC | 7874 |
rs7192015 | snp | C/T | 0.360632 | 0.224189 | intron-variant | USP7 | GRCh38.p7 | 16:8949358 | GATTGTTGGGTACTA[C/T]GTAGGGAAAAACTAC | 7874 |
rs7192587 | snp | C/T | 0.362732 | 0.22314 | intron-variant, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8949631 | ACCATGCCTTCCTTC[C/T]CTCAGAGTGCAATCT | 7874 |
rs7192659 | snp | C/T | 0.3744 | 0.216852 | intron-variant | USP7 | GRCh38.p7 | 16:8930900 | CTTGAACTCAGGAGG[C/T]GGAGGCTGCAGTGAG | 7874 |
rs7192755 | snp | G/T | 0.394354 | 0.204112 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8949685 | ATCTGCTCACCTCTG[G/T]GCATTCATCACCTTC | 7874 |
rs7195624 | snp | G/T | 0.46703 | 0.124089 | intron-variant | USP7 | GRCh38.p7 | 16:8916356 | CTTTATAACTAGACA[G/T]CTGCTGCCTTTTTGT | 7874 |
rs7199803 | snp | A/T | 0.48435 | 0.0870631 | intron-variant | USP7 | GRCh38.p7 | 16:8920948 | GGAACTCCCTTTGAA[A/T]GTCTGACTAAAAAGT | 7874 |
rs7200429 | snp | A/G/T | 0.0236746 | 0.106192 | intron-variant | USP7 | GRCh38.p7 | 16:8936150 | ATGAAGACCCAGCTC[A/G/T]GCCTCTGAGCCACAG | 7874 |
rs7202585 | snp | C/T | 0.0803491 | 0.183626 | intron-variant | USP7 | GRCh38.p7 | 16:8928910 | gagacatgtcatgac[C/T]gcaagtggagggCAG | 7874 |
rs7205293 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | USP7 | GRCh38.p7 | 16:8925559 | AAGGTACTCCTTAAA[C/T]ATTAAAAAGACCCAA | 7874 |
rs7342770 | snp | A/C | 0.310386 | 0.242597 | intron-variant | USP7 | GRCh38.p7 | 16:8940969 | TCAGGAATAGCAGGA[A/C]AGAATTCTCTCTCCT | 7874 |
rs8043595 | snp | C/G | 0.353371 | 0.227628 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937136 | CCTTACCAcacatca[C/G]taatcccaggcactt | 7874 |
rs8045445 | snp | A/G | 0.357877 | 0.225527 | intron-variant | USP7 | GRCh38.p7 | 16:8933494 | TCATATTCCCTTTAC[A/G]AAATTCAAAAGATGT | 7874 |
rs8048374 | snp | A/G | 0.0387552 | 0.1337 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937630 | aggctgcagtgagca[A/G]gggctgcaccactgc | 7874 |
rs8049394 | snp | A/G | 0.404384 | 0.196635 | intron-variant | USP7 | GRCh38.p7 | 16:8944047 | GAGACCCCCGTCTCT[A/G]AAATTAAAAACAAAC | 7874 |
rs8050609 | snp | A/T | 0.0603597 | 0.1629 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964180 | GCCCTGCGGAGGTGA[A/T]CCGGAATCCTTCCCA | 7874 |
rs8053087 | snp | A/T | 0.367091 | 0.220884 | intron-variant | USP7 | GRCh38.p7 | 16:8943978 | TAAAGCAAAACTATA[A/T]GGTGCGGGGGAGGCA | 7874 |
rs8054659 | snp | C/T | 0.379354 | 0.213933 | intron-variant | USP7 | GRCh38.p7 | 16:8955237 | TACATATTAATCTGT[C/T]TGCATTTCATTTCTA | 7874 |
rs8057254 | snp | A/T | 0.347473 | 0.230215 | intron-variant | USP7 | GRCh38.p7 | 16:8959132 | GCCTGGCGATTCCAG[A/T]CTCACAACAACCTTG | 7874 |
rs8059146 | snp | A/G | 0.372391 | 0.217992 | intron-variant | USP7 | GRCh38.p7 | 16:8939107 | accaacccaatgaag[A/G]tttctccacatttac | 7874 |
rs8060619 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | USP7 | GRCh38.p7 | 16:8939955 | ATACAAAAATTAGCC[A/G]AGCATGGTGGCACAT | 7874 |
rs8061621 | snp | C/T | 0.35574 | 0.226537 | intron-variant | USP7 | GRCh38.p7 | 16:8935151 | CCACCTTTTCGGAAG[C/T]TTTTAAGACATGGGG | 7874 |
rs8062134 | snp | C/G | 0.0700422 | 0.173537 | intron-variant | USP7 | GRCh38.p7 | 16:8955214 | TCTTTCCGTATGGCT[C/G]GTTTTTTTACATATT | 7874 |
rs8062960 | snp | C/G | 0.0707826 | 0.174302 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964090 | cggcaccgcctgcgc[C/G]gcagccccgcggcgg | 7874 |
rs9788866 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8903211 | TTTTCTAGTGACACG[A/G]AAGGAAGGTGGACGT | 7874 |
rs9922395 | snp | C/T | 0.420255 | 0.183066 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957496 | CACCTATAATCCCAG[C/T]GCTTTGAGAGGTTCA | 7874 |
rs9924441 | snp | C/T | 0.369754 | 0.219451 | intron-variant | USP7 | GRCh38.p7 | 16:8953341 | CCCAGCAGCCAGACC[C/T]GTTCCTGCCAGTCAG | 7874 |
rs9924609 | snp | C/T | 0.253264 | 0.249979 | intron-variant | USP7 | GRCh38.p7 | 16:8953554 | ACGTGCCCCATGCGG[C/T]GCCACCGGAAGCAGA | 7874 |
rs9926137 | snp | C/G | 0.34437 | 0.231505 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8951605 | GACCTGAGCGCATGA[C/G]GCTATACTTAGGTCT | 7874 |
rs9927018 | snp | A/G | 0.486133 | 0.082104 | intron-variant | USP7 | GRCh38.p7 | 16:8917926 | TCCCCAGTAGCTGGG[A/G]CTACAGGTGCACGCC | 7874 |
rs9928695 | snp | A/G | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8953587 | GAAGACACGTGCCCC[A/G]TGCGGCGCCACCGGA | 7874 |
rs9930206 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | USP7 | GRCh38.p7 | 16:8955320 | tgcaatcttggctca[A/C]tgtggcctcgacctc | 7874 |
rs9931153 | snp | C/T | 0.419296 | 0.183954 | intron-variant | USP7 | GRCh38.p7 | 16:8953521 | CCCATGCGGTGCCAC[C/T]GGAAGCAGAGGGAAG | 7874 |
rs9932027 | snp | C/G | 0.35809 | 0.225425 | intron-variant | USP7 | GRCh38.p7 | 16:8946543 | CGCGTATCTTACAAA[C/G]ACTCAAatctcaaat | 7874 |
rs9933060 | snp | C/T | 0.344592 | 0.231414 | intron-variant | USP7 | GRCh38.p7 | 16:8926199 | AAACAAAAGGTCggc[C/T]gggcgcggtggttcg | 7874 |
rs9934558 | snp | A/C | 0.379942 | 0.213577 | intron-variant | USP7 | GRCh38.p7 | 16:8955720 | AAAAAAAAAAAAAAA[A/C]AAAAAACATTGCACA | 7874 |
rs9936763 | snp | C/G | 0.34437 | 0.231505 | intron-variant | USP7 | GRCh38.p7 | 16:8953305 | GAGGCAGTCCCATCC[C/G]GGGTAGAGTTGAGAC | 7874 |
rs9937632 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | USP7 | GRCh38.p7 | 16:8918171 | ACTAGAATTACCCAT[A/G]CTGAGCTGTCCCTGG | 7874 |
rs9939495 | snp | A/T | 0.332568 | 0.235971 | intron-variant | USP7 | GRCh38.p7 | 16:8956152 | GATGTCAGGAAACCT[A/T]AGTTACTGGCATGTA | 7874 |
rs9940652 | snp | C/T | 0.478271 | 0.101943 | intron-variant | USP7 | GRCh38.p7 | 16:8921401 | CCATTTATGATTTCA[C/T]TGCTCTCTCCTTTCG | 7874 |
rs10163394 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP7 | GRCh38.p7 | 16:8914974 | ctatttaaacagaca[C/T]ctaaaacatgcaaag | 7874 |
rs10500365 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | USP7 | GRCh38.p7 | 16:8909117 | TCAACAAGCCTTCTA[C/T]GGGGACACCGGACTC | 7874 |
rs10500366 | snp | C/T | 0.448836 | 0.15154 | intron-variant | USP7 | GRCh38.p7 | 16:8955253 | TGCATTTCATTTCTA[C/T]ATGATGGACAGTATT | 7874 |
rs11075007 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | USP7 | GRCh38.p7 | 16:8896862 | CAACTGTCTTTGCAA[C/T]GGAGGCACACCCCAC | 7874 |
rs11075008 | snp | A/C | 0.18 | 0.24 | intron-variant | USP7 | GRCh38.p7 | 16:8897699 | AGACCCTGTCTCTAC[A/C]AAAAAAAAAAAAAAA | 7874 |
rs11075029 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | USP7 | GRCh38.p7 | 16:8921864 | TTCAAAAACCATACA[C/T]ACAGCACTTAAGCCA | 7874 |
rs11075031 | snp | A/C | 0.0471551 | 0.14613 | intron-variant | USP7 | GRCh38.p7 | 16:8922675 | TACTCCCAGAATCAA[A/C]TGGGTTTTTGATAAA | 7874 |
rs11075045 | snp | A/G | 0.402982 | 0.197728 | intron-variant | USP7 | GRCh38.p7 | 16:8940859 | TGAGGCAGGAGAATC[A/G]CTTATATACAGTGTC | 7874 |
rs11075053 | snp | G/T | 0.404907 | 0.196224 | intron-variant | USP7 | GRCh38.p7 | 16:8945477 | GGTTAGTGGGGGCTT[G/T]GGGAACAGTTCAACC | 7874 |
rs11551181 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893867 | ACTGAACAGCCTCAA[A/T]AAAATAAAATTAACA | 7874 |
rs11551182 | snp | A/G | 0.0444801 | 0.142343 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8905281 | TACTAAAGAGGAAGC[A/G]ATTGAGCACAATTAT | 7874 |
rs11551183 | snp | C/G | 0.0416632 | 0.138188 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8894835 | GCATTTTCGAGAAGT[C/G]ATGAAGCGAATCCAG | 7874 |
rs11642973 | snp | C/T | 0.106987 | 0.205054 | intron-variant | USP7 | GRCh38.p7 | 16:8929298 | ACCACACCCACACCA[C/T]TGCCCTCGTCTACGG | 7874 |
rs11644175 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8895269 | TTTTTGCTAAAAAAA[C/T]GCCACACCTGGATCC | 7874 |
rs11647769 | snp | A/C | 0.00835141 | 0.0640778 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956772 | cgtattaaaaaaaca[A/C]aaacaaaaaaaaaaa | 7874 |
rs11648031 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | USP7 | GRCh38.p7 | 16:8910409 | CTAAACACAGTCCAA[C/T]TTACTAAGAAATCCC | 7874 |
rs11649308 | snp | A/C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8897726 | aaaaaaaaaaaaaaa[A/C/T]atatatatatatata | 7874 |
rs11860575 | snp | C/G | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8953930 | GGCAGAGGGAAGACA[C/G]GTGCCCCCTGCGGCG | 7874 |
rs11862121 | snp | A/G | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8953548 | GAAGACACGTGCCCC[A/G]TGCGGCGCCACCGGA | 7874 |
rs11862147 | snp | A/G | 0.385168 | 0.210309 | intron-variant | USP7 | GRCh38.p7 | 16:8953642 | TGCGGCGCCACCGGA[A/G]GCAGAGGGAAGACAC | 7874 |
rs11862808 | snp | A/G | 0.00486615 | 0.0490856 | intron-variant | USP7 | GRCh38.p7 | 16:8903583 | TCAGGTATTTATTTA[A/G]AAAAGGAGGCTGTGg | 7874 |
rs11863279 | snp | A/G | 0.35445 | 0.227135 | intron-variant | USP7 | GRCh38.p7 | 16:8931666 | AAGTTACCACTGGTA[A/G]ATAAGGTGTAAATTA | 7874 |
rs11865187 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | USP7 | GRCh38.p7 | 16:8960074 | ATCTGAGTATTCAGA[A/G]GGCAGAGACCCATGC | 7874 |
rs11865642 | snp | A/C | 0.341909 | 0.232492 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956780 | AAAAACAAAAACAAA[A/C]AAAAAAAAACACTGA | 7874 |
rs12443510 | snp | A/T | 0.0414363 | 0.137845 | intron-variant | USP7 | GRCh38.p7 | 16:8939129 | cacatttacatgtac[A/T]tacgtgtatttagtt | 7874 |
rs12446090 | snp | C/T | 0.463126 | 0.13068 | intron-variant | USP7 | GRCh38.p7 | 16:8942595 | CTCTGTTGGGCAGGC[C/T]GGAGTGCAGTGGTGC | 7874 |
rs12446999 | snp | A/C | 0.44333 | 0.158505 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956474 | GGGGCATGCTAAGAA[A/C]TGAATTTGGGCCAGG | 7874 |
rs12447175 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8959518 | GACGTGCTCACATCA[G/T]AGTGAGATGCTAGGT | 7874 |
rs12447293 | snp | A/G | 0.0228947 | 0.104514 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962685 | GCGTTCCTTGCAGGT[A/G]TTTTCGAACGTAAGC | 7874 |
rs12448024 | snp | A/G | 0.444799 | 0.156695 | intron-variant | USP7 | GRCh38.p7 | 16:8930707 | GACATGGTGGCTCAT[A/G]CCTGTAATCCTAGCA | 7874 |
rs12449090 | snp | C/T | 0.480539 | 0.0967035 | intron-variant | USP7 | GRCh38.p7 | 16:8944260 | GCACAGCCAAAATAC[C/T]GGCTGAGGCTTGACA | 7874 |
rs12596001 | snp | G/T | 0.0722614 | 0.17581 | intron-variant | USP7 | GRCh38.p7 | 16:8909831 | cttgggaggctgagg[G/T]agaagaatcacttga | 7874 |
rs12600147 | snp | A/C | 0.443464 | 0.15834 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957775 | AATTAAAAAAAAAAC[A/C]AAAAAAAATTAAAAA | 7874 |
rs12708738 | snp | A/G | 0.490673 | 0.0676508 | intron-variant | USP7 | GRCh38.p7 | 16:8918829 | AGAAAAAGGTTGGCG[A/G]TGGTAACTCTGAATC | 7874 |
rs12917667 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8954094 | GAAGACACGTGCCCC[A/C]TGCGGCGCCACTGGA | 7874 |
rs12923175 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8955331 | ctcactgtggcctcg[A/C]cctccaaggttcaag | 7874 |
rs12923186 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8955357 | tcaagtgatcctccc[A/C]cctcggcctcccaaa | 7874 |
rs12924995 | snp | A/C | 0.480618 | 0.0965156 | intron-variant | USP7 | GRCh38.p7 | 16:8934788 | TTGGCCACCGAGTAC[A/C]TAAGGGGTGGGTCCC | 7874 |
rs12925019 | snp | C/T | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8954022 | ACGTGCCCCATGCGG[C/T]GCCACTGGAGGCAGA | 7874 |
rs12927752 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8955313 | gcagtgatgcaatct[G/T]ggctcactgtggcct | 7874 |
rs12927764 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8955342 | ctcgacctccaaggt[C/T]caagtgatcctccca | 7874 |
rs12927896 | snp | C/T | 0.0637235 | 0.166737 | intron-variant | USP7 | GRCh38.p7 | 16:8945111 | aaatacagaaattag[C/T]tgggtgtggtggcgg | 7874 |
rs12928761 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8954133 | GAAGACACGTGCCCC[A/C]TGCGGCGCCACTGGA | 7874 |
rs12929087 | snp | A/C | 0.466721 | 0.124627 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956782 | AAACAAAAACAAAAA[A/C]AAAAAAACACTGAAT | 7874 |
rs12929193 | snp | C/T | 0.44306 | 0.158832 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950305 | ACAGACATTTTCTGC[C/T]CTAAAAAAAAAGATG | 7874 |
rs12933724 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8894758 | CCTATGGCCCGCCAA[C/G]CCCCCAGGAGGCCCC | 7874 |
rs13330845 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8965166 | TCTCCCATTTATGTA[A/C]TGTTCATCTCCCTTC | 7874 |
rs13338372 | snp | A/G | 0.361894 | 0.223562 | intron-variant | USP7 | GRCh38.p7 | 16:8944922 | AGATCAGCCTGGCCA[A/G]TATGGCGAAACCTCG | 7874 |
rs13380483 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | USP7 | GRCh38.p7 | 16:8912517 | aagctgaaaccacca[C/T]ccatgatgaagacaa | 7874 |
rs16964658 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | USP7 | GRCh38.p7 | 16:8908521 | AATGAAAGCAACAGC[A/G]GTTCAGCAAGATTGG | 7874 |
rs16964664 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | USP7 | GRCh38.p7 | 16:8910332 | ACACTACTCATTCTA[A/T]AGTCGTGATCCTCAG | 7874 |
rs16964672 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | USP7 | GRCh38.p7 | 16:8911550 | AAAACAGCGCTGTCA[C/T]GCTCCGGACACATGC | 7874 |
rs16964691 | snp | C/G | 0.100769 | 0.200574 | intron-variant | USP7 | GRCh38.p7 | 16:8930425 | AAAAGAAATTCCACG[C/G]GTTTTACATTCATGG | 7874 |
rs17680450 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | USP7 | GRCh38.p7 | 16:8935939 | AGACCACTTCAGCAC[A/G]CGAATCTAACCCCTG | 7874 |
rs17747945 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | USP7 | GRCh38.p7 | 16:8934338 | CAGACTGAGACACAA[C/G]TGAATTCAGATTAGA | 7874 |
rs17747956 | snp | C/G | 0.0558544 | 0.157504 | intron-variant | USP7 | GRCh38.p7 | 16:8934571 | AAATGGTTCTAGTGT[C/G]AAGTTAGGGCTTCTC | 7874 |
rs17747980 | snp | A/C | 0.0562307 | 0.157967 | intron-variant | USP7 | GRCh38.p7 | 16:8939657 | TGTTTCACCTCCAGG[A/C]ATTCTCAATGTAATG | 7874 |
rs28362503 | in-del | -/C | | | intron-variant, frameshift-variant | USP7 | GRCh38.p7 | 16:8894538 | CCCGGTAAGGGTTCT[-/C]CCCCCCCCGGGGGCT | 7874 |
rs28481506 | snp | C/T | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8953677 | CCCGTGCGGCGCCAC[C/T]GGAGGCAGAGGGAAG | 7874 |
rs28482987 | snp | A/G | 0.437118 | 0.165792 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8965345 | GAGGTCGGGAGTTTG[A/G]GACCAGCCTGACCAA | 7874 |
rs28494891 | snp | A/G | 0.0310518 | 0.120672 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964093 | CACCGCCTGCGCCGC[A/G]GCCCCGCGGCGGACC | 7874 |
rs28507488 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8954032 | TGCGGCGCCACTGGA[A/G]GCAGAGGGAAGACAC | 7874 |
rs28523354 | snp | G/T | 0.404035 | 0.196909 | intron-variant | USP7 | GRCh38.p7 | 16:8946444 | AACTGTTGATCAACT[G/T]TGCTCCAGAAAGACT | 7874 |
rs28528233 | snp | A/C | 0.0314385 | 0.121371 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956789 | AACAAAAAAAAAAAA[A/C]CACTGAATTTGCTTT | 7874 |
rs28651477 | snp | A/G | 0.404384 | 0.196635 | intron-variant | USP7 | GRCh38.p7 | 16:8945025 | GGGAGACCAAGGCAG[A/G]TGAAAGACCTGAGGT | 7874 |
rs28673690 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8953626 | GAAGACACGTGCCCC[A/G]TGCGGCGCCACCGGA | 7874 |
rs28727382 | snp | C/G | 0.417034 | 0.18601 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956656 | GTAGTCCAGCTACTC[C/G]GGAGGCTGAGGCAGG | 7874 |
rs28740876 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8926321 | CGTCTCTACTAAAAA[A/T]AAAAAAAATTAGCTG | 7874 |
rs34147132 | in-del | -/A | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8958279 | TGGCCCCTGGGTGGG[-/A]ATTCTGAACCACTTT | 7874 |
rs34178482 | in-del | -/C | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8952077 | AAATAAAAAAGTAGA[-/C]CCCCCCGTCTATACA | 7874 |
rs34208767 | snp | C/G | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8953743 | GAAGACACGTGCCCC[C/G]TGCGGCGCCACTGGA | 7874 |
rs34236675 | in-del | -/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8901867 | GACAGAACAGGACGG[-/C]CCCCACGTGGCTGCT | 7874 |
rs34246823 | in-del | -/A | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8936764 | TGTCTTTAGGACCAG[-/A]AAACATTCAAGCAAC | 7874 |
rs34320939 | in-del | -/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8939749 | CTATTCACATTACGT[-/G]GGGTAAGTTTAATAA | 7874 |
rs34356795 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8902813 | GAATTGCTTGAAACC[-/A]AAAGGCGGAGGTTGC | 7874 |
rs34357840 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8916969 | CTACTCACTTGTCCT[-/A]AAAAAAAAAAAAAAA | 7874 |
rs34365795 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8910599 | TCTCCCTCCCCATTC[-/A]AATTATCCTACAAAC | 7874 |
rs34431715 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8900229 | AAGTAGGTACATTCT[-/A]AAGGAGTTTCGATTT | 7874 |
rs34434646 | in-del | -/A | 0.339429 | 0.233457 | intron-variant | USP7 | GRCh38.p7 | 16:8959356 | CAAAAAAAAAAAAAA[-/A]GGATACCTTCTTCCT | 7874 |
rs34474354 | in-del | -/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8906386 | GCTTGTGTTAACTTT[-/C]CTGATGAGCTTGCAT | 7874 |
rs34541874 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8933385 | ATTCCCAACTCTATT[-/A]AAAAACAAAAAAATT | 7874 |
rs34565009 | in-del | -/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8906314 | CCAGAGAATACATAG[-/C]ATCAGTTAGGGGTCC | 7874 |
rs34586799 | in-del | -/TT | | | intron-variant | USP7 | GRCh38.p7 | 16:8895855 | TTTTTTTTTTTTTTT[-/TT]GAGACAGTCTCAATC | 7874 |
rs34676056 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8948667 | AAGAAAAGGGAACGA[A/C]TACTGGCTACGATGT | 7874 |
rs34694496 | in-del | -/C | 0.0103295 | 0.0711199 | intron-variant | USP7 | GRCh38.p7 | 16:8910579 | TCCATCTCCCAACAT[-/C]CCCCCTCTCCCTCCC | 7874 |
rs34740188 | in-del | -/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8909583 | AATAGAGAACAGTAA[-/T]TTCTCGTCAACAGAC | 7874 |
rs34742987 | in-del | -/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8932669 | TCTTTCATCCACATT[-/C]CATTTTCCTTAGAAC | 7874 |
rs34812034 | in-del | -/TA | | | intron-variant | USP7 | GRCh38.p7 | 16:8929019 | GCTCCGCCCTATATC[-/TA]TGTCTCCTCCCAAGA | 7874 |
rs34816462 | in-del | -/C | 0.352721 | 0.227922 | intron-variant | USP7 | GRCh38.p7 | 16:8944904 | TGAGGTCAGGAGTTC[-/C]GAGATCAGCCTGGCC | 7874 |
rs34890846 | in-del | -/TTG | 0.372189 | 0.218105 | intron-variant | USP7 | GRCh38.p7 | 16:8947636 | ACAGGTGTGCGCTTA[-/TTG]TTTTTCAATCAATAA | 7874 |
rs34929337 | in-del | -/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8939797 | GATTTATCAACCACT[-/C]CCCTAAAGAAGACTG | 7874 |
rs34948058 | in-del | -/C | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957038 | GAATTCTGGAAGCAT[-/C]CCCTGCTCTGGCTCA | 7874 |
rs34972304 | in-del | -/AAAAATATATA/ATATATATA | | | intron-variant | USP7 | GRCh38.p7 | 16:8897727 | AAAAAAAAAAAAAAA[-/AAAAATATATA/ATATATATA]TATATATATATATAT | 7874 |
rs35018235 | snp | C/T | 0.000527131 | 0.0162261 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8910769 | TGGGGACAATAAATA[C/T]GACGCTGGGGAACAT | 7874 |
rs35021984 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8939685 | ATGTTCATATGTACA[C/T]ATCATGTACATTGCT | 7874 |
rs35031541 | in-del | -/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8958708 | CCCACACTCATCGCA[-/G]GGGAGCTCTAGCACT | 7874 |
rs35060100 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8926154 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAG | 7874 |
rs35081784 | in-del | -/AGAG | 0.443464 | 0.15834 | intron-variant | USP7 | GRCh38.p7 | 16:8932620 | TGCTAAATTTAAAAA[-/AGAG]AAAGAAAAGAAAAAT | 7874 |
rs35118185 | in-del | -/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8910293 | AGATGCCCAGAAACC[-/T]TGGGGGACACAACCC | 7874 |
rs35300417 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8954125 | GGCAGAGGGAAGACA[C/G]GTGCCCCCTGCGGCG | 7874 |
rs35354402 | in-del | -/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8901863 | TGAAGACAGAACAGG[-/G]ACGGCCCCACGTGGC | 7874 |
rs35380091 | in-del | -/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8935201 | GAGCTAAGGCACTAA[-/T]TTTTTTTTTTTTTTT | 7874 |
rs35427324 | in-del | -/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8943333 | TTACGCCTGTACTGC[-/T]TTCTACATGTATAGT | 7874 |
rs35628437 | in-del | -/A | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8940099 | CAAGACTCTGTCTCC[-/A]AAAAAAAAAGGCTGT | 7874 |
rs35654262 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8955489 | CACTTTGGGAGGCCG[-/A]AGTGAGGCAGCTCAT | 7874 |
rs35663109 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8892991 | ACGGGGCTGGGACCG[-/A]AAATAAAACTACACA | 7874 |
rs35685543 | in-del | -/A | 0.431621 | 0.171796 | intron-variant | USP7 | GRCh38.p7 | 16:8930973 | ACTCAGTCTCAAATT[-/A]AAAAAAAAAAAAAAA | 7874 |
rs35733519 | in-del | -/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8939314 | ATGTTCTGCATCTCT[-/G]GGGATCTTGTCACTT | 7874 |
rs35830769 | snp | A/G | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8898123 | TCACAGTGGGACCCA[A/G]AAGGGAAGGGTTGGC | 7874 |
rs35836333 | in-del | -/A | 0.302435 | 0.244439 | intron-variant | USP7 | GRCh38.p7 | 16:8929045 | CAAGACCTCCCCCCT[-/A]AAAAAAAAAAAGAAA | 7874 |
rs35853014 | in-del | -/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8941146 | CCATGCCCATGAGGA[-/C]CCCCCCGCCCCACCA | 7874 |
rs36002655 | in-del | -/A | 0.487589 | 0.0777925 | intron-variant | USP7 | GRCh38.p7 | 16:8944233 | GAGCAACAGAGGTGC[-/A]AAAAAAAAAAAGCAC | 7874 |
rs36003585 | in-del | -/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8932198 | AACAGGTATTACCAC[-/T]TCAGACGTTTAAGAC | 7874 |
rs36026136 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8916869 | GAGATAAAACAAAAT[A/C]CAATGATAAAAGCAC | 7874 |
rs36064651 | in-del | -/A | 0.479744 | 0.0985793 | intron-variant | USP7 | GRCh38.p7 | 16:8903868 | GTGAAACTCTGTCTC[-/A]AAAAAAAAAAAAAAG | 7874 |
rs36234555 | in-del | -/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8953629 | ACACGTGCCCCGTGC[-/G]GGCGCCACTGGAGGC | 7874 |
rs45513897 | snp | A/G | 0.08804 | 0.190444 | intron-variant | USP7 | GRCh38.p7 | 16:8915429 | AAATCATCTTTTAGA[A/G]CTGGTAGCCACATAC | 7874 |
rs55635828 | in-del | -/CAAAA | | | intron-variant | USP7 | GRCh38.p7 | 16:8897698 | AGACCCTGTCTCTAC[-/CAAAA]AAAAAAAAAAAAAAA | 7874 |
rs55678416 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | USP7 | GRCh38.p7 | 16:8923492 | CGACATGGAGTAAAC[C/T]GTTCTATACATCCTG | 7874 |
rs55680140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8958772 | CTACAGCATCAGTGG[C/T]GCATGGCACCAAATC | 7874 |
rs55688889 | in-del | -/AACGA/AACGATGTGGGGGTTTGTAGTTGCA/AACGATGTGGGGGTTTGTAGTTGCATCA/AACGATGTGGGGGTTTGTAGTTGCATCATTTAAAC | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8923206 | CCAGTAATGAAATAC[lengthTooLong]TGTCTTACGTGGAAT | 7874 |
rs55705409 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8954061 | ACGTGCCCCCTGCGG[C/T]GCCACTGGAGGCAGA | 7874 |
rs55727522 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893776 | TACCATAAAATAACT[C/T]TCATTGGCATCCAAG | 7874 |
rs55762241 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8954071 | TGCGGCGCCACTGGA[A/G]GCAGAGGGAAGACAC | 7874 |
rs55790221 | in-del | -/A | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938340 | TCAAAAAAAAAAAAA[-/A]GAAAGAAAGAAAGAA | 7874 |
rs55904070 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8953919 | GCGCCACTGGAGGCA[A/G]AGGGAAGACACGTGC | 7874 |
rs55937310 | in-del | -/AAAAA | 0 | 0 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892625 | AAAAAAAAAAAAAAA[-/AAAAA]GAAACAAGAGACCCT | 7874 |
rs55950454 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | USP7 | GRCh38.p7 | 16:8954765 | GTGGATCAGGAGATC[A/G]AGACCATCCATGGTA | 7874 |
rs56001050 | snp | C/G | 0.0086137 | 0.0650588 | intron-variant | USP7 | GRCh38.p7 | 16:8904590 | AAAGGCATCCTCTTT[C/G]ACCCCTGCAGATGGA | 7874 |
rs56011329 | in-del | -/T | 0 | 0 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937213 | GACTCTGTCTTTTTT[-/T]AAAAAAAAAAGGATT | 7874 |
rs56064469 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8944244 | TGCAAAAAAAAAAAA[-/A]GCACAGCCAAAATAC | 7874 |
rs56072147 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | USP7 | GRCh38.p7 | 16:8938888 | GATGTGTGAAGATTA[C/T]ATGCAAATACTACAC | 7874 |
rs56357547 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8892154 | CTTTCAGTTACCTAA[A/G]ACTACAGCCAACCCC | 7874 |
rs56410892 | snp | C/T | 0.367708 | 0.220556 | intron-variant | USP7 | GRCh38.p7 | 16:8941924 | TGGTGATCATTGCAA[C/T]AGAGGGCAAACGCAC | 7874 |
rs56828436 | snp | A/C | 0.0626037 | 0.165477 | intron-variant | USP7 | GRCh38.p7 | 16:8918740 | CTTGAACCCAGGAGA[A/C]AGAGGCTGCAGTGAG | 7874 |
rs56857425 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8930925 | AGTGAGCCAAGATCA[C/T]GCCACTGCACTCCAG | 7874 |
rs56874411 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | USP7 | GRCh38.p7 | 16:8909671 | AGTGGCTCATGCCTG[C/T]AATCCCAGCACTTTG | 7874 |
rs56907972 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | USP7 | GRCh38.p7 | 16:8900344 | GAAATTGAGAAGAGC[G/T]TTATGAGATGAAAAT | 7874 |
rs57051069 | snp | G/T | 0.0298908 | 0.118541 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893265 | TGCTCGTATGAACTG[G/T]TGAGATCGTAAGTCT | 7874 |
rs57130785 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957679 | GGGAGGATCACCTGA[A/G]CCCGGAAGTTTAAGG | 7874 |
rs57269467 | in-del | -/A | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8959370 | TCAAAAAAAAAAAAA[-/A]GGATACCTTCTTCCT | 7874 |
rs57461843 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8951142 | AGTCAAACCAAGTAA[C/G]GATTTCTGTATTTAA | 7874 |
rs57510291 | in-del | -/C | 0.0135883 | 0.0813171 | intron-variant | USP7 | GRCh38.p7 | 16:8916589 | ACAACTCCATTTAAA[-/C]GCTCAACTTTCAAAT | 7874 |
rs57594800 | in-del | -/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8897725 | AAAAAAAAAAAAAAA[-/T]AATATATATATATAT | 7874 |
rs57658828 | in-del | -/AA/AAA/AG | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8916986 | AAAAAAAAAAAAAAA[-/AA/AAA/AG]GAGGAAGCAGAATGG | 7874 |
rs57799800 | in-del | -/AT | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8929020 | CTCCGCCCTATATCT[-/AT]GTCTCCTCCCAAGAC | 7874 |
rs57805344 | in-del | -/A/AA | 0 | 0 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938711 | TCAAAAAAAAAAAAA[-/A/AA]TTGGGGGGACGGGGG | 7874 |
rs58029349 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8955726 | AAAAAAAAAAAAAAA[-/A]CATTGCACAGGGTCA | 7874 |
rs58502098 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937399 | ATACAAAAATTAGCC[A/T]GACGTGGTGGCGCAT | 7874 |
rs58598594 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8955581 | CATGGCGGCGCGCCC[C/T]TGTAGTCCTGGCTAC | 7874 |
rs58796383 | in-del | -/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8910831 | ATGATTCAAATACTT[-/T]AAAGAGAGAGAGAGA | 7874 |
rs59074916 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964601 | CACCCTCTCTACAAA[A/G]GTTTTGGGTTTTGTT | 7874 |
rs59161811 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8940763 | CTCTCCTAGGTGAAG[C/T]TCAAGCTGGCTTCAG | 7874 |
rs59246045 | in-del | -/GTT | | | intron-variant | USP7 | GRCh38.p7 | 16:8947638 | AGGTGTGCGCTTATT[-/GTT]TTTCAATCAATAAAC | 7874 |
rs59369679 | in-del | -/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8897724 | AAAAAAAAAAAAAAA[-/T]AAATATATATATATA | 7874 |
rs59410912 | in-del | -/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8897723 | AAAAAAAAAAAAAAA[-/T]AAAATATATATATAT | 7874 |
rs59532847 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8941071 | AGTGGTAGGTGCTGG[C/T]CAGGCCACACTGCCC | 7874 |
rs59591814 | snp | A/G | 0.153332 | 0.230554 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961222 | CACCGGCCAGGCGCG[A/G]TGGCTCACACCTGTA | 7874 |
rs59823804 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | USP7 | GRCh38.p7 | 16:8953359 | TCCTGCCAGTCAGCA[A/G]ATGTTTGATGAATGA | 7874 |
rs60023992 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8908808 | TTATGGAGAACCACA[A/G]AAAAATCATTAAATG | 7874 |
rs60094465 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8901321 | ACAAACAAAAAAACG[-/A]AAAAAAAAAAACAGT | 7874 |
rs60248986 | in-del | -/A | 0.431473 | 0.171952 | intron-variant | USP7 | GRCh38.p7 | 16:8904781 | TACTAAAAAAAAAAA[-/A]TAAAATAAAAATAAA | 7874 |
rs60302592 | snp | A/C | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8955719 | CAAAAAAAAAAAAAA[A/C]AAAAAAACATTGCAC | 7874 |
rs60467243 | in-del | -/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8896159 | TTTTTTTTTTTTTTT[-/T]AAAGAGGATCTGAAA | 7874 |
rs60556906 | snp | G/T | 0.0524604 | 0.153226 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961221 | ACACCGGCCAGGCGC[G/T]ATGGCTCACACCTGT | 7874 |
rs60623981 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8912462 | GTCAAAAAAAAAAAA[-/A]GAAAGAAAAAAGAAA | 7874 |
rs60657349 | in-del | -/AGGC | | | intron-variant | USP7 | GRCh38.p7 | 16:8914403 | GCACACCCTACAGGC[-/AGGC]CAGTAATCCTCTTCC | 7874 |
rs60750886 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8953813 | GGCAGAGGGAAGACA[C/G]GTGCCCCCTGCGGCG | 7874 |
rs60931912 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8897722 | AAAAAAAAAAAAAAA[A/T]AAAAATATATATATA | 7874 |
rs61280114 | in-del | -/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8897726 | AAAAAAAAAAAAAAA[-/T]ATATATATATATATA | 7874 |
rs61426394 | snp | C/G | 0.153997 | 0.230832 | intron-variant | USP7 | GRCh38.p7 | 16:8959662 | TTTGACTTTTGTCTC[C/G]TTACAGTGCTATTTG | 7874 |
rs61490845 | in-del | -/G | 0.0209421 | 0.100162 | intron-variant | USP7 | GRCh38.p7 | 16:8896914 | GGATCCCAGCTGGGT[-/G]GATTTCCACCAACGC | 7874 |
rs61731196 | snp | C/T | 0.0128748 | 0.0791936 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8895654 | TACCTCTATTCGAAA[C/T]GTCCGGCTCGTTGCA | 7874 |
rs61736975 | snp | G/T | 0.104938 | 0.20361 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8900548 | TGAAATACTATGATG[G/T]CACCATCCATTAGTT | 7874 |
rs62031299 | snp | A/G | 0.43555 | 0.167544 | intron-variant | USP7 | GRCh38.p7 | 16:8914180 | CCAATAAGCATTTGA[A/G]AAGGTAAGAACAACC | 7874 |
rs62031300 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8920562 | ATACTTTTTTTTTAA[A/T]TACATCCCAACTTTT | 7874 |
rs62031301 | snp | C/T | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8929268 | AAAACCTCCAAAAGC[C/T]CAACAACCAGCGAGA | 7874 |
rs62031302 | snp | A/C/T | 6.77312e-05 | 0.00581902 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8930396 | GTCATCTGTATCTCC[A/C/T]GCTTTAAAGAAGAAA | 7874 |
rs62031303 | snp | A/T | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8932612 | AATATACATGCTAAA[A/T]TTAAAAAAGAGAAAG | 7874 |
rs62031304 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | USP7 | GRCh38.p7 | 16:8940742 | GATCAATCCCCTCTG[C/T]GAGGCCTCTCCTAGG | 7874 |
rs62031305 | snp | G/T | 0.0271762 | 0.113356 | intron-variant | USP7 | GRCh38.p7 | 16:8942360 | CAAATATCAAGCAGT[G/T]GGGTCTGTCCCACCC | 7874 |
rs62031306 | snp | C/T | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8943838 | GATAAACACAAACAG[C/T]GCTTCGTGCACTGAT | 7874 |
rs62031322 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8959372 | AAAAAAAAAAAAAAG[A/G]ATACCTTCTTCCTAT | 7874 |
rs71155414 | in-del | -/G/GG/GGG | 0.592429 | 0.113053 | intron-variant, frameshift-variant, cds-indel | USP7 | GRCh38.p7 | 16:8894529 | GCCCCCGGGGGGGGG[-/G/GG/GGG]AGAACCCTTACCGGG | 7874 |
rs71155415 | in-del | -/A | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8897722 | AAAAAAAAAAAAAAA[-/A]TATATATATATATAT | 7874 |
rs71155416 | in-del | -/ATAT | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8897746 | TATATATATATATAT[-/ATAT]AAATGAGTTGGGCGT | 7874 |
rs71155420 | in-del | -/TAGAG | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8942082 | GCAGTCCAGGTAGAG[-/TAGAG]CAAACCGCAACAGGA | 7874 |
rs71155421 | in-del | -/TCAGGGAAACAGGCCCACATGGAAAATATTCAAAATATGCCACAAAAACAATAAATACCACACAGCCAGCTACAAGTTAATGAAGCAAGGAGACTG | 0 | 0 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8951269 | AATCTTTAAAATCTG[lengthTooLong]GCCTCTTAAGTCACC | 7874 |
rs71155423 | in-del | -/AA | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8955726 | AAAAAAAAAAAAAAA[-/AA]CATTGCACAGGGTCA | 7874 |
rs71155425 | in-del | -/GG | 0 | 0 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961516 | AAAGGGGGGGGGGGG[-/GG]CAAATACCTTGAAAT | 7874 |
rs71377192 | snp | A/G | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8896180 | GGATCTGAAATATCA[A/G]AAACAGAGACCGGAG | 7874 |
rs71377193 | snp | A/T | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8897721 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 7874 |
rs71378350 | multinucleotide-polymorphism | AC/CA | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8899011 | CTAAGCAAGAAATGG[AC/CA]TGTCAGGTGAAATGG | 7874 |
rs71386463 | snp | A/T | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8897723 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 7874 |
rs71386465 | snp | C/T | 0.408163 | 0.193609 | intron-variant | USP7 | GRCh38.p7 | 16:8953755 | CCCCTGCGGCGCCAC[C/T]GGAGGCAGAGGGAAG | 7874 |
rs71398459 | in-del | -/C | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8945129 | GTGTGGTGGCGGGCG[-/C]CCTGTAATCTCAGCT | 7874 |
rs71398460 | in-del | -/C | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8947607 | CCGCTTCAGCCTCCC[-/C]AAAATGCTGGGATTA | 7874 |
rs72768277 | snp | A/T | 0.0158469 | 0.0875917 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8892975 | CTCCAAAATAAAAGG[A/T]AACGGGGCTGGGACC | 7874 |
rs72768283 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | USP7 | GRCh38.p7 | 16:8911904 | ACAGGCTGGGAAGTC[C/T]GTGTTCCCACCAGCC | 7874 |
rs72768291 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | USP7 | GRCh38.p7 | 16:8939380 | AGTTGTTCCTTTCTC[C/T]TGTACTCTAGGATAT | 7874 |
rs72769903 | snp | A/G | 0.0197687 | 0.0974348 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8958186 | CCATCCCACCGGCAC[A/G]GTAGCAGGTGGGGCA | 7874 |
rs72769904 | snp | C/T | 0.0689305 | 0.172377 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962374 | AATCCAACACCCTTC[C/T]CTTTACAGCGTCTTC | 7874 |
rs73498861 | snp | A/C | 0.214541 | 0.247473 | intron-variant | USP7 | GRCh38.p7 | 16:8901299 | TGCTTAAAAAACAAA[A/C]AAACAAACAAACAAA | 7874 |
rs74010308 | snp | A/T | 0.0618563 | 0.164627 | intron-variant | USP7 | GRCh38.p7 | 16:8906217 | CCCAACATTGATTAC[A/T]CACAAAGAGAAGCAC | 7874 |
rs74010309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8907134 | GCTCACAGCCCCTGC[A/G]GCCTTCAGGAATGGT | 7874 |
rs74010317 | snp | C/T | 0.0293428 | 0.117518 | intron-variant | USP7 | GRCh38.p7 | 16:8921124 | ACAAGCAGTAATGCA[C/T]CAATTGTTCAGACTA | 7874 |
rs74010319 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | USP7 | GRCh38.p7 | 16:8926886 | TCTCACTACCTTCCA[A/G]TCTGGCCCCTGGAGA | 7874 |
rs74010322 | snp | A/C | 0.021333 | 0.101051 | intron-variant | USP7 | GRCh38.p7 | 16:8932354 | GAGAACTGCTTGAGC[A/C]CAGGAGTTTGAGACC | 7874 |
rs74010326 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | USP7 | GRCh38.p7 | 16:8934491 | AATGCGTAAGCTCTA[C/T]CCCCCATTTTTCAGC | 7874 |
rs74010330 | snp | A/G | 0.0569829 | 0.158885 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938243 | GATTCCTGTAGGACT[A/G]CTACTACACTATACT | 7874 |
rs74010333 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | USP7 | GRCh38.p7 | 16:8939413 | TGGCAGGGATGGACT[G/T]CCATTTGACCATTCA | 7874 |
rs74010335 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | USP7 | GRCh38.p7 | 16:8941074 | GGTAGGTGCTGGCCA[A/G]GCCACACTGCCCATG | 7874 |
rs74010342 | snp | C/G | 0.0524604 | 0.153226 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950493 | CTAATTCTTCCTCTC[C/G]AGACCCCTTACCCCA | 7874 |
rs74010344 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | USP7 | GRCh38.p7 | 16:8954542 | TCAAATCCACAATCT[A/G]TTTTTTGCAATGGAA | 7874 |
rs74010345 | snp | C/T | 0.0696718 | 0.173152 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956854 | CCCCCCCGCAGGCAG[C/T]GCCCCATTATCCACG | 7874 |
rs74010347 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | USP7 | GRCh38.p7 | 16:8958705 | CTTCCCCACACTCAT[C/T]GCAGGGAGCTCTAGC | 7874 |
rs74010349 | snp | A/G | 0.153332 | 0.230554 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960390 | CACTGCTGTTTTCCA[A/G]TGAATATACAAGGAC | 7874 |
rs74010351 | snp | A/G | 0.170408 | 0.236992 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962582 | CACCACACACTGCCA[A/G]GTACAAACTCCCCGA | 7874 |
rs74345065 | snp | G/T | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8895855 | TTTTTTTTTTTTTTT[G/T]TGAGACAGTCTCAAT | 7874 |
rs74483636 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | USP7 | GRCh38.p7 | 16:8900468 | AAATGTTTCTTGGTT[C/T]TACAACTTAAAAAAA | 7874 |
rs74488633 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | USP7 | GRCh38.p7 | 16:8895431 | CTAAATTCAAGTGAT[A/C]CACAGTTTCTGTCTG | 7874 |
rs74615182 | snp | A/G | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8947789 | GCTATTCCAGATGTG[A/G]GACTGCCTGATGGGT | 7874 |
rs74663583 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960663 | AGGTGCCAAGTCTCT[A/C]GCTCTGACCAGGACC | 7874 |
rs74680435 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | USP7 | GRCh38.p7 | 16:8933665 | ACAATGTTGCCCAGG[C/T]TGGTCTTGAACTGGA | 7874 |
rs74697944 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | USP7 | GRCh38.p7 | 16:8952836 | GCCTGTGACCACACT[C/T]GCTTTTTTTTTTTTA | 7874 |
rs74704148 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8947248 | ATTCCTCTCAATACA[A/C]TTTTGGAAAATAATT | 7874 |
rs74709536 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892710 | TTACAAATGCCAAGG[C/T]TTCCCAGGCCTGTTT | 7874 |
rs74728863 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8945720 | TCTAATATTTATATG[G/T]AACAATAAAAGATTG | 7874 |
rs74804559 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | USP7 | GRCh38.p7 | 16:8956175 | GGCATGTAATCAAAA[A/C]AGAGGGGCCTGGATT | 7874 |
rs74884198 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8945541 | CACTAGTGATGTACT[A/G]TGAATGCTAGCCATT | 7874 |
rs74916209 | snp | A/T | 0.0460142 | 0.144533 | intron-variant | USP7 | GRCh38.p7 | 16:8935942 | CCACTTCAGCACGCG[A/T]ATCTAACCCCTGAGA | 7874 |
rs75091998 | snp | C/T | 0.00392093 | 0.0441032 | intron-variant | USP7 | GRCh38.p7 | 16:8910878 | GCTTCATTTATAATG[C/T]AGCCAACACAGGTGT | 7874 |
rs75094587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8896739 | GGAAGGAGGAAAAAC[A/G]TGGCTTAATTGTGAA | 7874 |
rs75095558 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | USP7 | GRCh38.p7 | 16:8946560 | CTCAAATCTCAAATA[C/T]ATAAACAACAGTTCA | 7874 |
rs75122251 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP7 | GRCh38.p7 | 16:8960100 | CATGCAAGTCACTCC[C/T]TCAGCCCCTAGACTT | 7874 |
rs75153326 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | USP7 | GRCh38.p7 | 16:8896189 | ATATCAGAAACAGAG[A/G]CCGGAGGCAAGGCAC | 7874 |
rs75172776 | snp | A/G | 0.081446 | 0.184634 | intron-variant | USP7 | GRCh38.p7 | 16:8907957 | ATATTGGAAAATCCT[A/G]TTTAAACGAATACAC | 7874 |
rs75219349 | snp | C/T | 0.0785177 | 0.181917 | intron-variant | USP7 | GRCh38.p7 | 16:8913653 | ACCCGCACTAAATGA[C/T]TCCTAACGAGAATCC | 7874 |
rs75238810 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893664 | GCAGCCGAGCCACTC[C/G]TGCCCACTAGGGACA | 7874 |
rs75445219 | snp | C/T | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8952838 | CTGTGACCACACTCG[C/T]TTTTTTTTTTTTAAG | 7874 |
rs75464564 | snp | C/T | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8896142 | CCATGCCCAGCTTTT[C/T]TTTTTTTTTTTTTTT | 7874 |
rs75508194 | snp | A/G | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8909936 | GTCTCAGAAAAAAAA[A/G]CAACTTTCTGATCTA | 7874 |
rs75556177 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | USP7 | GRCh38.p7 | 16:8936064 | GCAGGGGGCGGGGGT[C/T]GCGAACACAATACAA | 7874 |
rs75578838 | snp | A/C/G | 0.571429 | 0.170747 | intron-variant | USP7 | GRCh38.p7 | 16:8953782 | GAAGACACGTGCCCC[A/C/G]TGCGGCGCCACTGGA | 7874 |
rs75593824 | snp | C/T | 0.0460142 | 0.144533 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950819 | AGCGCACGACAGTGA[C/T]CTGAGCGGGCACTAT | 7874 |
rs75782533 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP7 | GRCh38.p7 | 16:8919670 | GAATTAACTGTGTCT[C/T]GTACCTTCCCACCCC | 7874 |
rs75811744 | snp | G/T | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8941325 | TTAGCTAGGATTTCA[G/T]GCATCCCCTAAAGGG | 7874 |
rs75830058 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8947060 | AGAGAATAGTCAATC[A/G]TTCAAAAAGGCTACT | 7874 |
rs75917951 | snp | C/G | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8947786 | TTAGCTATTCCAGAT[C/G]TGGGACTGCCTGATG | 7874 |
rs75959309 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | USP7 | GRCh38.p7 | 16:8929683 | GTGACTGTGCAAATA[C/T]TGAGGTCACTAATTT | 7874 |
rs75971563 | snp | A/G | 0.00277872 | 0.0371704 | intron-variant | USP7 | GRCh38.p7 | 16:8900522 | ACAATCCTTCACAAA[A/G]TACATACTTCTGAAA | 7874 |
rs76010282 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8928844 | AAGGGGACTTTACCC[A/G]TATTGTCCCCTCATA | 7874 |
rs76020431 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957544 | AGACCAGGAATTCCA[C/T]ACCAGCCTGAACATA | 7874 |
rs76147374 | snp | G/T | 0.0279689 | 0.115005 | intron-variant | USP7 | GRCh38.p7 | 16:8916854 | GTGTCTATTTCCAAA[G/T]AGATAAAACAAAATA | 7874 |
rs76161145 | snp | C/T | 0.0463947 | 0.145069 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957090 | AAGAAACGTACTAAT[C/T]ACTGTTTCCAACTTC | 7874 |
rs76175628 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | USP7 | GRCh38.p7 | 16:8901618 | CACAGCAATAAAAGT[C/T]TGTCATTTTATAGCA | 7874 |
rs76217886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8928643 | GCCATCAGAAAGATA[C/T]TACATGCTGGGTCTT | 7874 |
rs76268321 | snp | A/C | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8930644 | TTTGCTTTATTTGCA[A/C]TGATATTCTGCACAA | 7874 |
rs76311746 | snp | A/G/T | 0.000742065 | 0.019249 | intron-variant | USP7 | GRCh38.p7 | 16:8916990 | AAAAAAAAAAAAGAG[A/G/T]AAGCAGAATGGCAAA | 7874 |
rs76368597 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | USP7 | GRCh38.p7 | 16:8921016 | ACGAAACTGGAGAAA[A/G]CATGTTTTCAAAGAC | 7874 |
rs76384592 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | USP7 | GRCh38.p7 | 16:8958781 | CAGTGGCGCATGGCA[C/G]CAAATCCACTTGACT | 7874 |
rs76395097 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | USP7 | GRCh38.p7 | 16:8938917 | ACTGTTTTGTATGAG[G/T]AAGACTTGAGCATCT | 7874 |
rs76426500 | snp | A/C | 0.046775 | 0.145601 | intron-variant | USP7 | GRCh38.p7 | 16:8906872 | TATCTGCAAACTGAG[A/C]AACATGAAAAATCAA | 7874 |
rs76435791 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8918009 | GTTAGCCAGGATGGT[C/G]TCGATCTGCTGACCT | 7874 |
rs76501830 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892622 | AAAAAAAAAAAAAAA[A/G]AAAAAAAGAAACAAG | 7874 |
rs76531043 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8918191 | GCTGTCCCTGGGATA[A/T]ATCACGACAACCTGT | 7874 |
rs76569125 | snp | C/T | 0.0194246 | 0.0969811 | intron-variant | USP7 | GRCh38.p7 | 16:8958586 | TCTGAGACAGCCAAA[C/T]GGGCCTGGCAACAGG | 7874 |
rs76682701 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | USP7 | GRCh38.p7 | 16:8954704 | TTGCAGGCCGGGCAC[A/G]GTGGACTCACACCTG | 7874 |
rs76769473 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | USP7 | GRCh38.p7 | 16:8904259 | CTGCCCTGCTGTGCA[A/G]TGACCCAAGGGGTCC | 7874 |
rs76802066 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | USP7 | GRCh38.p7 | 16:8905696 | ACTGAGCACACCAAA[A/C]GAGAGTTCAAATTTT | 7874 |
rs76835623 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP7 | GRCh38.p7 | 16:8952097 | CCGTCTATACAAAAA[A/G]GAAAAAAAATGGCCA | 7874 |
rs76857105 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8943485 | CTGGATGGAGATCTG[A/C/T]GACACACAAGAGCCA | 7874 |
rs76951557 | snp | A/C | 0.0463947 | 0.145069 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8949882 | AGTTATTACATGAAA[A/C]TGCTTGGCTTTCCAT | 7874 |
rs76991861 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | USP7 | GRCh38.p7 | 16:8909958 | TCTGATCTATACCTC[A/G]GTCCCTCAGTCCAAC | 7874 |
rs77022371 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | USP7 | GRCh38.p7 | 16:8936219 | CAACCTAGTGATCAA[A/G]ACTACAGCTGTTATT | 7874 |
rs77026442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8948496 | GGCCCCCAGTTAACT[C/T]AACTTAGTAAGTGAA | 7874 |
rs77059570 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8955910 | TTGGAAACACACCTC[C/T]CAACTTTTTCTGAAG | 7874 |
rs77119485 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | USP7 | GRCh38.p7 | 16:8912864 | TTCATTTTCAAACTT[A/G]TTAAATTTTTTTTTA | 7874 |
rs77188284 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | USP7 | GRCh38.p7 | 16:8932242 | TTCAGTCTTGATAGT[C/T]TCTTAATACACTTAA | 7874 |
rs77217719 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | USP7 | GRCh38.p7 | 16:8900904 | GTAGACCTAACACTG[C/T]AACAAATTCGGGGTA | 7874 |
rs77315566 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP7 | GRCh38.p7 | 16:8955030 | TCTGCTCAGCTACCA[C/T]GAGATGAATGACAGT | 7874 |
rs77387014 | snp | A/G | 0.0123036 | 0.0774623 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957861 | TATTTATGAAAGTCT[A/G]TCAATGTCTTTGTCT | 7874 |
rs77597904 | snp | A/C | 0.5 | 0 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938341 | GAAATAACACAGTCA[A/C]AAAAAAAAAAAGAAA | 7874 |
rs77657542 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | USP7 | GRCh38.p7 | 16:8929199 | CCTCAGAGCTGGCCA[C/T]GCCTTCCCAAATGCA | 7874 |
rs77797543 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | USP7 | GRCh38.p7 | 16:8914350 | ATTGATAAACCACTT[C/T]GGGAATCTCGCTAAC | 7874 |
rs77809369 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | USP7 | GRCh38.p7 | 16:8958591 | GACAGCCAAACGGGC[C/T]TGGCAACAGGATGTG | 7874 |
rs77863729 | snp | A/C | 0.0463947 | 0.145069 | intron-variant | USP7 | GRCh38.p7 | 16:8949328 | GAAACTGAGACATAA[A/C]AATGCAATGCAATTG | 7874 |
rs77864036 | snp | A/T | | | stop-gained, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8898382 | CTAAATTGGCTGTTT[A/T]ACCATATACATTTAA | 7874 |
rs77888871 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | USP7 | GRCh38.p7 | 16:8905429 | GTGTGAACTTCTAGG[C/T]ATGCCCCTAGTTGAA | 7874 |
rs77912250 | snp | C/G | 0.00259889 | 0.035954 | intron-variant | USP7 | GRCh38.p7 | 16:8903441 | GAAAAGACTTGACAA[C/G]TGACAAAAAATGAGT | 7874 |
rs77998839 | snp | C/G/T | 3.29496e-05 | 0.00405881 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8894848 | ATCACTTCTCGAAAA[C/G/T]GCTCGCCCTAGAATG | 7874 |
rs78001601 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | USP7 | GRCh38.p7 | 16:8940224 | ATCCTATAGCCAGGT[A/C]ACCTGTCTAGGCATC | 7874 |
rs78090277 | snp | C/T | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8952839 | TGTGACCACACTCGC[C/T]TTTTTTTTTTTAAGA | 7874 |
rs78131890 | snp | A/C | 0.5 | 0 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956790 | ACAAAAAAAAAAAAA[A/C]ACTGAATTTGCTTTA | 7874 |
rs78136109 | snp | A/G | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8959370 | TCAAAAAAAAAAAAA[A/G]GGATACCTTCTTCCT | 7874 |
rs78153282 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8918193 | TGTCCCTGGGATATA[A/T]CACGACAACCTGTCT | 7874 |
rs78181501 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | USP7 | GRCh38.p7 | 16:8935563 | GACTGGGGACATGTT[C/T]GGCAAACACAAGTGA | 7874 |
rs78330977 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8955016 | GTTTCACACAACATT[C/G]TGCTCAGCTACCACG | 7874 |
rs78384191 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | USP7 | GRCh38.p7 | 16:8904983 | TCAAAAAAATAAAAT[A/T]AAATAATCTATTAAC | 7874 |
rs78398661 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | USP7 | GRCh38.p7 | 16:8928003 | TTAGCCACACATGGC[A/G]GTACTTCCTTGGTCA | 7874 |
rs78412750 | snp | A/C | 0.5 | 0 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956770 | TTCGTATTAAAAAAA[A/C]AAAAACAAAAAAAAA | 7874 |
rs78480835 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | USP7 | GRCh38.p7 | 16:8952492 | GTTCTAGGGGGAAAT[G/T]TTTCCCTGCCGCTTC | 7874 |
rs78530845 | snp | A/G | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8912462 | GTCAAAAAAAAAAAA[A/G]GAAAGAAAAAAGAAA | 7874 |
rs78631947 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8943433 | CACGGCCGGAACCGA[A/G]CTGCACAGATGCAGT | 7874 |
rs78655336 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | USP7 | GRCh38.p7 | 16:8931112 | TACAGCCAATTTTGT[C/T]GTGAAGATTACTGAA | 7874 |
rs78665874 | snp | A/T | 0.0463947 | 0.145069 | intron-variant | USP7 | GRCh38.p7 | 16:8946413 | TGGTGAAACCGCATC[A/T]CTAAATAAAGAAAAA | 7874 |
rs78846691 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8927851 | AAAATAAAATAAAAT[A/G]AAACTTCCTTGGGCC | 7874 |
rs78861615 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | USP7 | GRCh38.p7 | 16:8916072 | TGATTAGTGATGGCG[C/T]GGGGAGAGTAATCAC | 7874 |
rs78870959 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | USP7 | GRCh38.p7 | 16:8928190 | ATTTAGCATCTTACA[A/C]AAGAAATGTCCCTTA | 7874 |
rs78893115 | snp | C/T | 0.0681886 | 0.171594 | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891877 | CCGCTGTGAAGACTC[C/T]GAATGCTGTCAACAG | 7874 |
rs78932417 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | USP7 | GRCh38.p7 | 16:8943615 | CCTCTGCTGGATTAA[C/T]GGTGAAAAGCAATGG | 7874 |
rs79003022 | snp | A/T | 0.0230942 | 0.104948 | intron-variant | USP7 | GRCh38.p7 | 16:8895185 | ACACAGTTCTGTAAG[A/T]GCAAGTGATGTGGTC | 7874 |
rs79028709 | snp | G/T | 0.0263992 | 0.111815 | intron-variant | USP7 | GRCh38.p7 | 16:8915641 | TAGACTATAAAAATA[G/T]GACCTCTGGCATGCA | 7874 |
rs79069946 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | USP7 | GRCh38.p7 | 16:8901621 | AGCAATAAAAGTCTG[C/T]CATTTTATAGCAAGG | 7874 |
rs79077420 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938352 | GTCAAAAAAAAAAAA[A/G]GAAAGAAAGAAAGAA | 7874 |
rs79190405 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP7 | GRCh38.p7 | 16:8945814 | CCAGCACTTTAGGAA[A/G]CCAAGGCAAGAAGAC | 7874 |
rs79203539 | snp | C/T | 0.0700422 | 0.173537 | intron-variant | USP7 | GRCh38.p7 | 16:8955435 | GTTTTAAAATAGCAA[C/T]TGCATGGCCAGGCGC | 7874 |
rs79235555 | snp | G/T | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8933772 | ACTTTTTTTTTTTTT[G/T]TGAGATGGAGTCTTC | 7874 |
rs79274429 | snp | C/G | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8953774 | GGCAGAGGGAAGACA[C/G]GTGCCCCCTGCGGCG | 7874 |
rs79294513 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | USP7 | GRCh38.p7 | 16:8925853 | CTTCATACTAGCAGA[A/G]TAATTGAAAACTTTT | 7874 |
rs79327950 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8945887 | GAGACCCCACTTCCA[A/G]AAAAAAAGTAAAAAT | 7874 |
rs79341389 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | USP7 | GRCh38.p7 | 16:8946160 | CACCTTATACAAAAG[A/G]TAGCTCACAATGAAA | 7874 |
rs79430602 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | USP7 | GRCh38.p7 | 16:8912067 | GACTTACAAGTCACT[C/T]ATCTGTGCATAAGAG | 7874 |
rs79464581 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | USP7 | GRCh38.p7 | 16:8941449 | CAGGAAGGACCTGAG[A/G]GGTAAAGGCACGTAT | 7874 |
rs79490679 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8956203 | ATTTTTTAATCTTCT[A/G]TGGCAGGCAGGAAAA | 7874 |
rs79493421 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8908008 | ACATTTATAATCGGT[C/G]AAAATTAAATTTATT | 7874 |
rs79518720 | snp | G/T | | | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8898379 | TCCCTAAATTGGCTG[G/T]TTAACCATATACATT | 7874 |
rs79557410 | snp | A/T | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8932615 | ATACATGCTAAATTT[A/T]AAAAAGAGAAAGAAA | 7874 |
rs79570814 | snp | A/G | 0.039522 | 0.134904 | intron-variant | USP7 | GRCh38.p7 | 16:8918390 | TTAAAATTTTCAATA[A/G]AAGTAAGTTGCATTG | 7874 |
rs79622552 | snp | A/C | 0.0547245 | 0.156101 | intron-variant | USP7 | GRCh38.p7 | 16:8912460 | ATGTCAAAAAAAAAA[A/C]AAGAAAGAAAAAAGA | 7874 |
rs79666243 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | USP7 | GRCh38.p7 | 16:8910967 | ACTCTCCCCCTGTAG[C/T]CAAGACTGTAGGTAA | 7874 |
rs79682514 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | USP7 | GRCh38.p7 | 16:8934679 | ATCCAAATTAACACA[C/T]CTGACTTGGTGTGGC | 7874 |
rs79753148 | snp | A/C | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8912450 | GTGAGACTCCATGTC[A/C]AAAAAAAAAAAAGAA | 7874 |
rs79753385 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | USP7 | GRCh38.p7 | 16:8942240 | ACAGGAAGCCATCCA[C/T]GTCCTTGGGAGGTAC | 7874 |
rs79792761 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | USP7 | GRCh38.p7 | 16:8900043 | TCTCCTCTACAGGAG[A/C]AGACCCAGACGCAGT | 7874 |
rs79832036 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8925604 | CAGAATTGAAGTTTG[C/T]ACTTGGTTCACCTGC | 7874 |
rs79848265 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8949565 | TTACCTCCAAATCCC[C/G]GAGCTCAAGTCCTAA | 7874 |
rs79862794 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8912664 | GACACAGGGCTGGGC[A/G]TGGTCCCAGCACTTC | 7874 |
rs79882961 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP7 | GRCh38.p7 | 16:8907588 | TGGCCGGGTGTGGTG[A/G]TTCACGCCAGTAATC | 7874 |
rs79920553 | in-del | -/AAAA | | | intron-variant | USP7 | GRCh38.p7 | 16:8901329 | AAAAACGAAAAAAAA[-/AAAA]CAGTAAGCTGAATAG | 7874 |
rs79926513 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP7 | GRCh38.p7 | 16:8897292 | CTGGCCCTAATCTAG[A/G]ACCAACCAAATACTG | 7874 |
rs79980775 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8932621 | GCTAAATTTAAAAAA[A/G]AGAAAGAAAAGAAAA | 7874 |
rs79983710 | snp | A/C | 0.5 | 0 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938710 | AGCAAGACTCCGTCT[A/C]AAAAAAAAAAAAATT | 7874 |
rs80043052 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | USP7 | GRCh38.p7 | 16:8940127 | TGTTTCCATCCAGGT[C/T]TTTCCTGTATTTTTG | 7874 |
rs80072736 | snp | C/T | 0.00279162 | 0.0372561 | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891634 | ATCAGGAAGCGATGG[C/T]GTCTAGACGTGGCTT | 7874 |
rs80159161 | snp | A/G | 0.0295035 | 0.117819 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956594 | ACATGGTGAAACGCC[A/G]TCTCTACTAAAATAT | 7874 |
rs80249909 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | USP7 | GRCh38.p7 | 16:8959711 | TATAATCACAACAGC[A/G]CAAGTTTATCTGGCT | 7874 |
rs80267105 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | USP7 | GRCh38.p7 | 16:8929311 | CATTGCCCTCGTCTA[C/G]GGTGGAAAGCGCACT | 7874 |
rs80320919 | snp | C/G | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8933328 | AAGACGGGACGATCA[C/G]ATAAGTCAAGGAGTC | 7874 |
rs111356144 | snp | A/G/T | 0.0700422 | 0.173537 | intron-variant | USP7 | GRCh38.p7 | 16:8954243 | GCAGAGGGAAGACAC[A/G/T]TGCCCCCTGCGGTGC | 7874 |
rs111358261 | snp | C/T | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8948403 | TTGCCCAGGCTGATC[C/T]CAAACCCCTGGGCTC | 7874 |
rs111380428 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964140 | CCCGGGCCCTGGGGG[A/C]CGAGGCGGGCCGCCC | 7874 |
rs111398653 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8925011 | AAAGGCAAGAAACTT[A/G]TTTAAGATAATAACG | 7874 |
rs111436450 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | USP7 | GRCh38.p7 | 16:8952959 | CTCCTGCCTCGGCCT[A/C]CCAAGTAGCTGGGAT | 7874 |
rs111440926 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | USP7 | GRCh38.p7 | 16:8942752 | CTGGGTCTCACTATG[C/T]TGTCCAGGCTGGTCT | 7874 |
rs111450753 | snp | A/G | 0.0032017 | 0.0398823 | intron-variant | USP7 | GRCh38.p7 | 16:8903245 | GAGCCACGGTGGGGT[A/G]TATCCACGGGACCGG | 7874 |
rs111457059 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | USP7 | GRCh38.p7 | 16:8919226 | CTGACTCAAGGTCAG[C/T]CTTAAGGAAACCGAG | 7874 |
rs111471248 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8953707 | GACACGTGCCCCGTG[C/T]GGCGCCACCGGAGGC | 7874 |
rs111487169 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8953763 | GCGCCACTGGAGGCA[A/G]AGGGAAGACACGTGC | 7874 |
rs111518278 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | USP7 | GRCh38.p7 | 16:8926295 | CCAGCCTGCCCAACA[C/T]GGTGAAACCCCGTCT | 7874 |
rs111529376 | snp | G/T | 0.00303224 | 0.0388192 | intron-variant | USP7 | GRCh38.p7 | 16:8899081 | GAACTGTGGAAAGCA[G/T]GCAGTCAAGACCAAG | 7874 |
rs111530057 | snp | A/G | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8905799 | CAGACTGAAGTCAAC[A/G]TAGCATGTTCCTAAC | 7874 |
rs111537953 | snp | A/G | 0.00149837 | 0.0273302 | intron-variant | USP7 | GRCh38.p7 | 16:8919014 | AAGGCTGCAGGAGAG[A/G]AACACTATCCATTTA | 7874 |
rs111561877 | snp | A/G | 0.00159848 | 0.0282256 | intron-variant | USP7 | GRCh38.p7 | 16:8916569 | CACCTTTCAAAGATA[A/G]AACAAACAACTCCAT | 7874 |
rs111584803 | snp | C/T | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8901984 | ATCAACACATCTTTC[C/T]GCAAGGGAAGAAGGC | 7874 |
rs111608726 | in-del | -/G | 0 | 0 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961505 | CTCAAAAAAAAAAAA[-/G]GGGGGGGGGGGCAAA | 7874 |
rs111693286 | in-del | -/A | 0.5 | 0 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957591 | CAAAACTTAAAATTC[-/A]AAAAAAAAAAAAAAA | 7874 |
rs111714395 | snp | A/G | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8953876 | TGCGGCGCCACTGGA[A/G]GCAGAGGGAAGACAC | 7874 |
rs111731536 | in-del | -/A | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8927320 | GAAAAAAAGAAAAAG[-/A]AAAAAAAAAAAGAAA | 7874 |
rs111792557 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | USP7 | GRCh38.p7 | 16:8894721 | AAAAAAGCCTAGGCC[A/G]CTACGCTAGGCAAGG | 7874 |
rs111792818 | snp | A/T | 0.162253 | 0.234095 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8965384 | AACCCCGTCTCTACT[A/T]AAAGTACAAAATTAG | 7874 |
rs111813044 | snp | C/T | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8959745 | TGTGTTCAAGAGAAC[C/T]CACATTCTACTCCCA | 7874 |
rs111878156 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | USP7 | GRCh38.p7 | 16:8903125 | TTCTCAGGCAGGAAA[C/T]GTTCCTGGGTCACAC | 7874 |
rs111887065 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8953604 | GCGGCGCCACCGGAA[A/G]CAGAGGGAAGACACG | 7874 |
rs111924957 | snp | A/G | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8953603 | TGCGGCGCCACCGGA[A/G]GCAGAGGGAAGACAC | 7874 |
rs111984267 | in-del | -/C | 0.0543475 | 0.155628 | intron-variant | USP7 | GRCh38.p7 | 16:8910212 | ACCAGCAGCCAGAAA[-/C]AGCCCATTTCCCTTC | 7874 |
rs111991783 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | USP7 | GRCh38.p7 | 16:8905514 | GGCAGCGCCTCAGGC[A/G]TCCGCTCATACAATT | 7874 |
rs112011807 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | USP7 | GRCh38.p7 | 16:8949367 | GTACTATGTAGGGAA[A/C]AACTACTGTTCGAGG | 7874 |
rs112027715 | snp | A/G | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8913249 | TAATCCCAGCTACTT[A/G]TGAGCCTAAGGCAGG | 7874 |
rs112060619 | snp | A/C | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8934136 | TTACCCTACGACAAT[A/C]GCTTTAAAACATGGT | 7874 |
rs112094088 | snp | C/T | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8953632 | ACGTGCCCCGTGCGG[C/T]GCCACCGGAAGCAGA | 7874 |
rs112094515 | snp | A/C/G | 0.000444719 | 0.0149051 | intron-variant | USP7 | GRCh38.p7 | 16:8894776 | CCCAGGAGGCCCCAG[A/C/G]TGCACACCTTCTCAA | 7874 |
rs112122697 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | USP7 | GRCh38.p7 | 16:8919953 | CGCTCACCATGTTAG[C/T]TGTCGGTGATGCTCA | 7874 |
rs112142733 | in-del | -/T | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8915599 | AATTTTATAATTGAC[-/T]AGAAATATCAATGTT | 7874 |
rs112181883 | snp | A/G | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8953798 | TGCGGCGCCACTGGA[A/G]GCAGAGGGAAGACAC | 7874 |
rs112183132 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893973 | CCCACACACCGTCCT[C/T]GCCTTGAACACACCA | 7874 |
rs112192844 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | USP7 | GRCh38.p7 | 16:8900373 | ATGTTCACCACACCT[A/C]ATTTCAAAACCCAGA | 7874 |
rs112208591 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | USP7 | GRCh38.p7 | 16:8924862 | TATTTCACATAACCC[A/T]GCTGAGTTGCTTACA | 7874 |
rs112214295 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8923841 | CTTTACAGAGCACGG[A/G]ACACACAGGCAGGAC | 7874 |
rs112232576 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | USP7 | GRCh38.p7 | 16:8922511 | CTGGGGGATCTGACA[C/G]AACAGCCAGAGTCAG | 7874 |
rs112251519 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | USP7 | GRCh38.p7 | 16:8953132 | AGCCACTATGCCTGG[C/T]CTCACCACCTCTTTT | 7874 |
rs112317998 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | USP7 | GRCh38.p7 | 16:8906094 | GCACGCAGAGGGACA[A/T]GCGACCAGCCAGCCT | 7874 |
rs112322468 | snp | A/G | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8908197 | TTCCTTTAACACTGC[A/G]GCTCTTGGGACACAG | 7874 |
rs112378910 | snp | A/C/G | 0.00795532 | 0.062565 | intron-variant | USP7 | GRCh38.p7 | 16:8905030 | CCATAAGTCTGCATC[A/C/G]AAACGCGCAAGCCCA | 7874 |
rs112380399 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | USP7 | GRCh38.p7 | 16:8911880 | GGGGAACAACCTTCA[C/G]AGCTCACGACAGGCT | 7874 |
rs112387204 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8934146 | ACAATAGCTTTAAAA[C/T]ATGGTTTTAATGCAT | 7874 |
rs112412316 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | USP7 | GRCh38.p7 | 16:8933131 | TTTTAGTAGAGACAG[C/G]GTTTCATCATGTTGG | 7874 |
rs112415721 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | USP7 | GRCh38.p7 | 16:8925747 | CTCACACTCAAGGCA[C/T]ATTTCTTAGAACAGA | 7874 |
rs112457721 | snp | C/G | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8897170 | CCACAAAGGAAGAGA[C/G]GAGAAAGTTGCATCA | 7874 |
rs112459633 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | USP7 | GRCh38.p7 | 16:8899352 | TAATGAATCACCATG[C/G]GAGTAGCATATCTGA | 7874 |
rs112471677 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | USP7 | GRCh38.p7 | 16:8910678 | CAAATTTTTATTTAG[C/T]AATTAAAAGAATTGA | 7874 |
rs112493057 | snp | C/G | 0.0463947 | 0.145069 | intron-variant | USP7 | GRCh38.p7 | 16:8953513 | ACACGTGCCCCATGC[C/G]GTGCCACTGGAAGCA | 7874 |
rs112498852 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | USP7 | GRCh38.p7 | 16:8926131 | TGCACTCTAGCCTGG[C/G]CGACAGAGCGAGACT | 7874 |
rs112500982 | snp | A/T | 0.00227254 | 0.0336319 | intron-variant | USP7 | GRCh38.p7 | 16:8915370 | GGAAAGTAAAAGTGG[A/T]TTAACTAGTAATAGT | 7874 |
rs112547349 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | USP7 | GRCh38.p7 | 16:8932344 | GCAAAGATGGGAGAA[C/G]TGCTTGAGCCCAGGA | 7874 |
rs112554965 | snp | C/T | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8953593 | ACGTGCCCCATGCGG[C/T]GCCACCGGAAGCAGA | 7874 |
rs112584677 | snp | A/G | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8894767 | CGCCAAGCCCCCAGG[A/G]GGCCCCAGCTGCACA | 7874 |
rs112592775 | snp | G/T | 0.00159617 | 0.0282053 | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891789 | TTCAGCTCGCTGCTC[G/T]TGTGTGTGAGGGCGT | 7874 |
rs112644069 | snp | A/G | 0.5 | 0 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8902102 | TTATCAAACTTGGGT[A/G]AGGTCGCTCCACTAG | 7874 |
rs112651183 | snp | A/G | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8932332 | GCACTCTGGGAGGCA[A/G]AGATGGGAGAACTGC | 7874 |
rs112668046 | snp | C/T | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8903144 | CCTGGGTCACACTCC[C/T]CACTGTTAGGCAGTG | 7874 |
rs112677679 | in-del | -/A | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8948977 | TGTCTCCCAAAGGGG[-/A]AAAAAAAAAGCTTAC | 7874 |
rs112696348 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP7 | GRCh38.p7 | 16:8947490 | ATTAGCTGGACTACA[A/G]ACATGCACCACCACA | 7874 |
rs112755106 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | USP7 | GRCh38.p7 | 16:8928402 | AAAACTTATTTTGGA[G/T]AAGCAATTTATGCTG | 7874 |
rs112772703 | in-del | -/A | 0.0659589 | 0.169201 | intron-variant | USP7 | GRCh38.p7 | 16:8895261 | AAGCCTATTTTTGCT[-/A]AAAAAAACGCCACAC | 7874 |
rs112777575 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | USP7 | GRCh38.p7 | 16:8896724 | TCAGAAGATACAAGG[A/G]GAAGGAGGAAAAACG | 7874 |
rs112778544 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP7 | GRCh38.p7 | 16:8905002 | TAATCTATTAACATG[A/G]AATTACTTGGTACCA | 7874 |
rs112816608 | in-del | -/A | 0 | 0 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957764 | CCTGTCTCTTAAATT[-/A]AAAAAAAAACAAAAA | 7874 |
rs112874101 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | USP7 | GRCh38.p7 | 16:8902608 | AAGACTGTGATCGTA[A/G]GCCAGGTGCTGTGGC | 7874 |
rs112935927 | in-del | -/T | 0.00953873 | 0.0683987 | intron-variant | USP7 | GRCh38.p7 | 16:8920550 | TAGAGATGAAAATAC[-/T]TTTTTTTTTAAATAC | 7874 |
rs112990130 | snp | G/T | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8959730 | GTTTATCTGGCTGGG[G/T]GTGTTCAAGAGAACT | 7874 |
rs113023041 | snp | A/C/G | 0.0663714 | 0.169821 | intron-variant | USP7 | GRCh38.p7 | 16:8947353 | CACAGCACTCCCCCC[A/C/G]CCAACACACACACAC | 7874 |
rs113025474 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8923756 | CTTGGAGAGAAGGAA[C/T]GACATGGCTCATATC | 7874 |
rs113056477 | snp | C/T | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8929038 | TCTCCTCCCAAGACC[C/T]CCCCCCTAAAAAAAA | 7874 |
rs113075321 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | USP7 | GRCh38.p7 | 16:8942771 | CCAGGCTGGTCTTGA[A/G]CTCCTGGCCTCAAGC | 7874 |
rs113078572 | snp | A/G | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8894898 | ACAGTCACTCCCAGC[A/G]CCCCCAGGCCACGTC | 7874 |
rs113120899 | snp | A/G | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8919273 | ACACAGCATCCTTCA[A/G]TGGTCACCGATTCCC | 7874 |
rs113122381 | snp | C/T | 0.5 | 0 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8908412 | TTGTAGATGTAACAC[C/T]GGTGGCAATGTTAGG | 7874 |
rs113125486 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | USP7 | GRCh38.p7 | 16:8917535 | AGGCACGCACCACCA[C/T]GCCAGGCTAATTTAT | 7874 |
rs113148479 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | USP7 | GRCh38.p7 | 16:8926003 | ACCAAAACTACAAAA[A/C]ATTAGCCGGGTGCAG | 7874 |
rs113177770 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | USP7 | GRCh38.p7 | 16:8905499 | ACGGTGTGCTAGGCA[A/G]GCAGCGCCTCAGGCA | 7874 |
rs113213518 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | USP7 | GRCh38.p7 | 16:8906343 | CCCTGACAAGGTTCC[A/G]AGTAGGAACCAGAAC | 7874 |
rs113218139 | snp | C/T | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8920693 | CTCAGTGCCACAGCA[C/T]GGACAGGAGAAATCT | 7874 |
rs113252937 | in-del | -/A | 0.0972767 | 0.197928 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937214 | ACTCTGTCTTTTTTT[-/A]AAAAAAAAAGGATTA | 7874 |
rs113343775 | in-del | -/A | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8912450 | TCAAAAAAAAAAAAA[-/A]GAAAGAAAAAAGAAA | 7874 |
rs113345778 | snp | C/T | 0.0103295 | 0.0711199 | downstream-variant-500B, nc-transcript-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8892073 | AGGGAACGCGGCAGA[C/T]GACGGAAACATTACA | 7874 |
rs113373249 | snp | A/G | 0.5 | 0 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8902182 | ATTATCACTGAGCTC[A/G]ATCATCTATTTCCAA | 7874 |
rs113410530 | snp | A/G | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8923452 | TCACAGAGCCTGTGC[A/G]TTGACCAAAAGCACT | 7874 |
rs113436337 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8932610 | CAAATATACATGCTA[A/C]ATTTAAAAAAGAGAA | 7874 |
rs113456437 | snp | C/T | 0.375 | 0.216506 | intron-variant | USP7 | GRCh38.p7 | 16:8953911 | CCCATGCGGCGCCAC[C/T]GGAGGCAGAGGGAAG | 7874 |
rs113472188 | snp | C/G | 0.0422008 | 0.138995 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961507 | CAAAAAAAAAAAAGG[C/G]GGGGGGGGGCAAATA | 7874 |
rs113516556 | snp | A/G | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8953993 | TGCGGCGCCACTGGA[A/G]GCAGAGGGAAGACAC | 7874 |
rs113528786 | snp | C/T | 1.76877e-05 | 0.00297381 | intron-variant | USP7 | GRCh38.p7 | 16:8908491 | TGTAGTTAGCCTCTA[C/T]TTACTCCTGGAAGCA | 7874 |
rs113545079 | snp | A/G | 0.00210368 | 0.0323638 | missense, utr-variant-5-prime, intron-variant | USP7 | GRCh38.p7 | 16:8936595 | CACCTTCCAGCCCAA[A/G]CCTGTGGTTCCCAGC | 7874 |
rs113548050 | snp | C/T | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8953950 | CCCCTGCGGCGCCAC[C/T]GGAGGCAGAGGGAAG | 7874 |
rs113556549 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | USP7 | GRCh38.p7 | 16:8919192 | TACCCCATTGCTCCT[A/G]CAGTGTGTGTGAAGC | 7874 |
rs113637481 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | USP7 | GRCh38.p7 | 16:8930472 | AAAATATAAACTTAT[A/C]CTTTTGATGTTGCCT | 7874 |
rs113645462 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | USP7 | GRCh38.p7 | 16:8918532 | AATTAGGTCATGGCT[C/G]GGCATGGTGGATCAT | 7874 |
rs113646803 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | USP7 | GRCh38.p7 | 16:8919239 | AGCCTTAAGGAAACC[A/G]AGGCCAGGAACACTT | 7874 |
rs113676052 | snp | G/T | 0.0013763 | 0.0261965 | intron-variant | USP7 | GRCh38.p7 | 16:8899208 | GACACAGAAAGGAAG[G/T]TTCACATTTTGGGGA | 7874 |
rs113678581 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | USP7 | GRCh38.p7 | 16:8917366 | AAAACATAAGAATGC[A/G]AAAATAAATTTTGAA | 7874 |
rs113679434 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP7 | GRCh38.p7 | 16:8941918 | GTCCCTTGGTGATCA[C/T]TGCAATAGAGGGCAA | 7874 |
rs113794586 | snp | A/C/G | 0.0115224 | 0.075102 | intron-variant | USP7 | GRCh38.p7 | 16:8952856 | TTTTTTTTTTAAGAC[A/C/G]GAGTCTCATTCTTGT | 7874 |
rs113810711 | in-del | -/A | 0 | 0 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938340 | AGAAATAACACAGTC[-/A]AAAAAAAAAAAAGAA | 7874 |
rs113813738 | in-del | -/A | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8914757 | CCCCATCTCTTAACC[-/A]AAAAAAAAAAAATTA | 7874 |
rs113828262 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | USP7 | GRCh38.p7 | 16:8907430 | ACTCTCCCTTAAACC[C/T]GAAGGCTGAATGACC | 7874 |
rs113860336 | snp | C/T | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8953638 | CCCGTGCGGCGCCAC[C/T]GGAAGCAGAGGGAAG | 7874 |
rs113915986 | in-del | -/C | 0 | 0 | intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8963058 | GACTTTGCAGCCTCG[-/C]CAGGCCGGGGCCGGG | 7874 |
rs113947582 | snp | A/G | 0.0696718 | 0.173152 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957497 | ACCTATAATCCCAGT[A/G]CTTTGAGAGGTTCAG | 7874 |
rs113966488 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | USP7 | GRCh38.p7 | 16:8912392 | GAGACAAAGGTTGTA[C/G]TGAGCTGAGACTGCA | 7874 |
rs113975818 | snp | G/T | 0.0554779 | 0.157039 | intron-variant | USP7 | GRCh38.p7 | 16:8925914 | AATCACAGCACTTTG[G/T]GAGGCAGAGGCGGGT | 7874 |
rs113978907 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8916070 | AGTGATTAGTGATGG[C/T]GCGGGGAGAGTAATC | 7874 |
rs114019746 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | USP7 | GRCh38.p7 | 16:8907420 | ATTTGATTACACTCT[C/T]CCTTAAACCTGAAGG | 7874 |
rs114118349 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8897994 | AGCTTGGGGAGTAAG[C/T]GCAGAGTCATGGACT | 7874 |
rs114141717 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | USP7 | GRCh38.p7 | 16:8947337 | TGGTTTATTGTTTTT[C/G]CACAGCACTCCCCCC | 7874 |
rs114159725 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | USP7 | GRCh38.p7 | 16:8922517 | GATCTGACAGAACAG[A/C]CAGAGTCAGTTCACT | 7874 |
rs114199899 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | USP7 | GRCh38.p7 | 16:8954818 | ACAAAAAAATTAGCC[A/G]GTGCGGTGAGGGGCG | 7874 |
rs114286936 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | USP7 | GRCh38.p7 | 16:8899929 | TCCCTCTGTAAGCGA[A/G]GCAAGTATGCATGGG | 7874 |
rs114347515 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | USP7 | GRCh38.p7 | 16:8945646 | CCCCAAATTAATCCA[C/T]ACATTTAAACACAGT | 7874 |
rs114484601 | snp | A/G | 0.00716266 | 0.059414 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964620 | TTGGGTTTTGTTTTT[A/G]TATTTTTGAAATGTA | 7874 |
rs114525882 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | USP7 | GRCh38.p7 | 16:8907094 | AGCACAGCATGCACC[C/T]GGCCTGCGAAGCAGC | 7874 |
rs114529350 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP7 | GRCh38.p7 | 16:8938869 | AATTTAAACTATATA[A/G]GAAGATGTGTGAAGA | 7874 |
rs114539916 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | USP7 | GRCh38.p7 | 16:8940733 | GTGGAGTGAGATCAA[A/T]CCCCTCTGCGAGGCC | 7874 |
rs114731909 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8903161 | ACTGTTAGGCAGTGG[C/G]TGGACACAGCACCTA | 7874 |
rs114733683 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | USP7 | GRCh38.p7 | 16:8933613 | CACACTATGTGTATG[C/T]GCTATCATTTTTTTT | 7874 |
rs114762380 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | USP7 | GRCh38.p7 | 16:8902546 | TAGTCCTCTATATTA[C/T]ACACACATATGTATA | 7874 |
rs114787305 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | USP7 | GRCh38.p7 | 16:8945845 | TGCTTGAGGCCAGGA[A/G]TCAGAAACCAGCCTG | 7874 |
rs114819809 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | USP7 | GRCh38.p7 | 16:8953437 | CTACTGCCACTAAGT[A/C]AAGTCTGAGGTACGA | 7874 |
rs114863685 | snp | A/T | 0.000955708 | 0.021839 | intron-variant | USP7 | GRCh38.p7 | 16:8901107 | TAATGTACTGAGCAA[A/T]ATCTACTCAGAAGGT | 7874 |
rs114956279 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | USP7 | GRCh38.p7 | 16:8927511 | GGAGAACAACATTCT[A/C]AATCTAGATCCATCT | 7874 |
rs115019180 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8928446 | AACCCTGAGACATAC[A/G]ACAGTAAATAAAGCT | 7874 |
rs115047762 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP7 | GRCh38.p7 | 16:8917563 | TATGAATTTTCAGGA[A/G]AGACAGGGTTTTGCC | 7874 |
rs115131954 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | USP7 | GRCh38.p7 | 16:8912854 | CTTCTAAAAATAAAA[A/G]AAAATTTAAAAAGTT | 7874 |
rs115196512 | snp | C/T | 0.00874735 | 0.0655527 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8936800 | TTTAGATAAGGCAGT[C/T]CAGGAACAGAAGAGG | 7874 |
rs115208920 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | USP7 | GRCh38.p7 | 16:8933553 | CTACTAGAGATTAGG[G/T]TTACATAGAAGCAAT | 7874 |
rs115252995 | snp | C/T | 0.0217236 | 0.101931 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8949722 | CATTATTTGCTCATA[C/T]GACCTATCTGAACCC | 7874 |
rs115256200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8959323 | ATGAATTTTTACTTA[A/G]TGACCTCTTTCTCCT | 7874 |
rs115445511 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938306 | CTTTGAGATAACTGT[A/G]GATTCACACACAGTC | 7874 |
rs115456196 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | USP7 | GRCh38.p7 | 16:8935069 | ATTGTTCAAGACAGA[C/T]GTACAACATTGGCAT | 7874 |
rs115484176 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | USP7 | GRCh38.p7 | 16:8909913 | CCTGGGGAACAGACC[A/G]AGTCTCCGTCTCAGA | 7874 |
rs115493166 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | USP7 | GRCh38.p7 | 16:8919404 | CAAGCCCAGCACCAA[C/G]AGACACTTAACGGAG | 7874 |
rs115585847 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | USP7 | GRCh38.p7 | 16:8923792 | AAGGACGGGACTTCT[A/G]GGGGTAAAGACCACG | 7874 |
rs115622995 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | USP7 | GRCh38.p7 | 16:8927530 | CTAGATCCATCTAGA[G/T]CTTCAGAGGCCGTAT | 7874 |
rs115805100 | snp | C/T | 0.0422008 | 0.138995 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961035 | CCTCTGCCATCCAAT[C/T]TGAGATTCTGCTAAA | 7874 |
rs115935836 | snp | A/G | 0.0142736 | 0.0832652 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938639 | ATGGCATGAACCTGG[A/G]AAGCAGAGTTGCAGT | 7874 |
rs116253007 | snp | A/T | 0.0422008 | 0.138995 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961190 | AATTCAACACCCTCT[A/T]GTCTTTTAAAAGCAA | 7874 |
rs116286079 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8956021 | CCATGTTCCGCAATA[C/G]AAGTCACACTACCAA | 7874 |
rs116375961 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8953202 | GAGGCTCCCCCTCCC[C/T]GCGGTAAGCCAGTCC | 7874 |
rs116394727 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | USP7 | GRCh38.p7 | 16:8912819 | ATAAAGATTTTCATT[A/T]AAAAAAAATCCAAGT | 7874 |
rs116542245 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | USP7 | GRCh38.p7 | 16:8905882 | GCTGCTGTTACACGC[A/C]CTCTTCACTGTTCTC | 7874 |
rs116601124 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | USP7 | GRCh38.p7 | 16:8946913 | TAAAACTTGATGAAT[C/T]CATATTTTCCAAACG | 7874 |
rs116634140 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8902273 | AAGTATTGAAGAAAA[C/T]GTCCAATTCTAGTTA | 7874 |
rs116762731 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | USP7 | GRCh38.p7 | 16:8946561 | TCAAATCTCAAATAT[A/T]TAAACAACAGTTCAC | 7874 |
rs116768762 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | USP7 | GRCh38.p7 | 16:8900117 | CCGTGAGTCAGGAAA[G/T]CTGGGCTTTCGTGTG | 7874 |
rs116834314 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | USP7 | GRCh38.p7 | 16:8928307 | GCCCTAGTCTGAAAT[A/G]GACACTCAACACTCA | 7874 |
rs116918051 | snp | C/T | 0.0260105 | 0.111035 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964225 | ACACCCCGAAAGACC[C/T]AGGAGCGGCAATGAG | 7874 |
rs116926411 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8905014 | ATGAAATTACTTGGT[A/C]CCATAAGTCTGCATC | 7874 |
rs116953593 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8907578 | AAACTACTTGTGGCC[A/G]GGTGTGGTGGTTCAC | 7874 |
rs117137129 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | USP7 | GRCh38.p7 | 16:8922207 | AGAAAATGAAAGTAC[A/G]GCCAGGTGCGCTGGC | 7874 |
rs117169990 | snp | A/C | 0.0460142 | 0.144533 | intron-variant | USP7 | GRCh38.p7 | 16:8932799 | GGGGATGGACAAAGC[A/C]GGATAGTGCCTTATC | 7874 |
rs117176121 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | USP7 | GRCh38.p7 | 16:8952995 | TCGCGTGTCACCATG[C/T]CAGGCTATTTTTTGT | 7874 |
rs117184416 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | USP7 | GRCh38.p7 | 16:8948587 | ACAGATGACACAATC[C/G]TAAGAACCTGCACAT | 7874 |
rs117253745 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | USP7 | GRCh38.p7 | 16:8953190 | GAGGCCTCACCTGAG[A/G]CTCCCCCTCCCCGCG | 7874 |
rs117436339 | snp | A/G | 0.00716266 | 0.059414 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8958241 | CCAACAGGGAGAGGC[A/G]ACTAGAAAGGCTTAG | 7874 |
rs117439328 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | USP7 | GRCh38.p7 | 16:8933265 | TTAAAAAAATTTAGC[C/T]AAGCACAGTGGCTCA | 7874 |
rs117439738 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | USP7 | GRCh38.p7 | 16:8945426 | AGACTAGTTGTCCAG[A/C]GAGTAGCAAAGGAAA | 7874 |
rs117441525 | snp | C/T | 0.00716266 | 0.059414 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8892908 | GAAAAATAAGAGTGA[C/T]TTGCTGATTCTATTT | 7874 |
rs117470077 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP7 | GRCh38.p7 | 16:8952794 | GTCTGGCAGTTCCCA[A/G]ACTCATCCTGCTATT | 7874 |
rs117630458 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | USP7 | GRCh38.p7 | 16:8913969 | CCTCAAACTCCTGGG[C/T]TCAAGCAATCCTCCC | 7874 |
rs117654423 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8901826 | TCTGACCAACGTGAT[C/T]AGCACAGCACAGCAG | 7874 |
rs117697595 | snp | C/T | 0.0460142 | 0.144533 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938372 | GAAAGAAAGAAATAA[C/T]ACAGTCAAGTCTTCC | 7874 |
rs117757700 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP7 | GRCh38.p7 | 16:8954737 | ATCCCAGCACTTTGG[A/G]GGTCTGAGGTGGGTG | 7874 |
rs117822796 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | USP7 | GRCh38.p7 | 16:8946419 | AACCGCATCTCTAAA[C/T]AAAGAAAAAAACTGT | 7874 |
rs117905082 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | USP7 | GRCh38.p7 | 16:8905605 | GGCAATTTTTATAAT[A/C]TACTGAAATAGCCCA | 7874 |
rs118105617 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | USP7 | GRCh38.p7 | 16:8943550 | CATGAGAAACACAAA[C/T]GACTAACCAACAGGC | 7874 |
rs118109545 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | USP7 | GRCh38.p7 | 16:8920803 | TGTTCCACTGGTTAC[C/T]ACCTCTGCAAAAAGC | 7874 |
rs118119613 | snp | A/G | 0.0021284 | 0.0325526 | intron-variant | USP7 | GRCh38.p7 | 16:8930268 | GTTTCCGCCCACTGC[A/G]AGGCGGTGAACCACA | 7874 |
rs118147217 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | USP7 | GRCh38.p7 | 16:8947594 | CTCAAGTGATCCACC[A/C]GCTTCAGCCTCCCAA | 7874 |
rs118177314 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | USP7 | GRCh38.p7 | 16:8932184 | TTCAAAATACCAAGA[A/C]ACAGGTATTACCACT | 7874 |
rs137881743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950319 | CTCTAAAAAAAAAGA[C/T]GGGACCCAGTGCTCT | 7874 |
rs137886097 | snp | A/G | 4.94173e-05 | 0.00497053 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894070 | TTTGTTGAAGTGGTC[A/G]AGCCCTAGCCAAGGC | 7874 |
rs137890734 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | USP7 | GRCh38.p7 | 16:8909874 | GAGGTTGCAGTGAGT[C/G]GAGATCGCGCCACTG | 7874 |
rs138005920 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8912426 | CTGCACTCCAGCCGG[C/G]GCGACAGAGTGAGAC | 7874 |
rs138031088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8926633 | AAATAGTTAACAGTA[C/T]ACTGGATCCTATGTA | 7874 |
rs138049921 | in-del | -/CAT | 0.0126979 | 0.078662 | intron-variant | USP7 | GRCh38.p7 | 16:8932468 | AACTAGTCCCTAGAC[-/CAT]CATGTCTTGACAGAA | 7874 |
rs138060270 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8933644 | TCCTCAAAGAGACAA[A/G]ATTTTACAATGTTGC | 7874 |
rs138106837 | snp | A/G | 0.00438332 | 0.0466095 | downstream-variant-500B, nc-transcript-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8892077 | AACGCGGCAGATGAC[A/G]GAAACATTACAACAC | 7874 |
rs138108712 | in-del | -/CA | | | intron-variant | USP7 | GRCh38.p7 | 16:8941121 | GCCCAATTCACATGG[-/CA]GGCCCATGCCCCATG | 7874 |
rs138135688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8956183 | ATCAAAAAAGAGGGG[C/T]CTGGATTTTTTAATC | 7874 |
rs138145767 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP7 | GRCh38.p7 | 16:8913770 | TATTTTACTTTCTTG[A/G]GAGAGATACTTGCTC | 7874 |
rs138174560 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8944231 | AGAGCAACAGAGGTG[-/A]CAAAAAAAAAAAAGC | 7874 |
rs138182723 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | USP7 | GRCh38.p7 | 16:8913975 | ACTCCTGGGTTCAAG[C/G]AATCCTCCCGACTCA | 7874 |
rs138207509 | in-del | -/TTTTCTGAATTAGGTC | 0.436408 | 0.16659 | intron-variant | USP7 | GRCh38.p7 | 16:8916404 | AAACAAAGATGGGCA[-/TTTTCTGAATTAGGTC]TGAGGTTTTACTTGG | 7874 |
rs138265327 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | USP7 | GRCh38.p7 | 16:8905542 | ATTCACCAGGACCTT[C/T]GCAGTCCCCATTCAA | 7874 |
rs138273658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962378 | CAACACCCTTCTCTT[C/T]ACAGCGTCTTCACAT | 7874 |
rs138273822 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | USP7 | GRCh38.p7 | 16:8933969 | ACCATGTTGGCCAGG[C/G]TGGTCTCAAACTCAT | 7874 |
rs138331860 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8940135 | TCCAGGTTTTTCCTG[C/T]ATTTTTGTGACTCCA | 7874 |
rs138338712 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960347 | TTCCTAACTGCTCAG[A/G]GCATTTCAAAAAATA | 7874 |
rs138352786 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | USP7 | GRCh38.p7 | 16:8894934 | GCAGCCGCCAAAACC[A/G]ACGCCTAACCCCAGC | 7874 |
rs138374668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8928555 | TGCGCAATTTGTACT[A/G]CAGCTGGAAAACGCT | 7874 |
rs138402630 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8921976 | GACAAGGGTAGGACA[C/G]TGCTGTTCCCACAGC | 7874 |
rs138406884 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | USP7 | GRCh38.p7 | 16:8936286 | GTGGCTCACATGGCG[C/T]CCTACAGCCCATCTC | 7874 |
rs138414736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8953472 | AGGGGAAACCAAGAC[A/G]GTAAGAAACGGGGGT | 7874 |
rs138453954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8898014 | AGTCATGGACTGCTC[C/T]GTTCACAGGCCTGCT | 7874 |
rs138487464 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP7 | GRCh38.p7 | 16:8923783 | TATCTGTTCAAGGAC[A/G]GGACTTCTGGGGGTA | 7874 |
rs138490551 | snp | A/C/G | 0.00226452 | 0.0335761 | intron-variant | USP7 | GRCh38.p7 | 16:8895755 | GCCTGAACAGAGAGG[A/C/G]AAAAAAAATAGGGCA | 7874 |
rs138650792 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8931169 | AAATATTTTAAACGT[G/T]TTCATCATGAACACA | 7874 |
rs138700330 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | USP7 | GRCh38.p7 | 16:8909651 | AGCAACTTTCTGGAT[A/G]AGCAAGTGGCTCATG | 7874 |
rs138702600 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8940098 | CAAGACTCTGTCTCC[-/A]AAAAAAAAAAGGCTG | 7874 |
rs138732932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8947207 | AACAGACAATAAAGA[A/G]ATTTACAAAAATGTA | 7874 |
rs138766744 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP7 | GRCh38.p7 | 16:8933467 | CCTGTGTTGAAATAG[A/G]AATATATAATTTCAT | 7874 |
rs138768698 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | USP7 | GRCh38.p7 | 16:8910311 | GGGGACACAACCCTA[C/G]AGAACACACTACTCA | 7874 |
rs138883007 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | USP7 | GRCh38.p7 | 16:8926311 | GGTGAAACCCCGTCT[C/T]TACTAAAAATAAAAA | 7874 |
rs138918649 | snp | C/T | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892719 | CCAAGGTTTCCCAGG[C/T]CTGTTTCCAGGGAGA | 7874 |
rs138945109 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962660 | GCCAGTCCAAAACCT[A/G]ACAACATCTGCGTTC | 7874 |
rs138948322 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8942146 | CAGGGCCAAAGCTAT[A/G]GAGGGCCTTGAAGGC | 7874 |
rs138991949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8921658 | AGTGCCATGCCTCTC[A/G]AGCTCTCCTAGGATG | 7874 |
rs139012432 | snp | A/T | 0.0475351 | 0.146656 | intron-variant | USP7 | GRCh38.p7 | 16:8939939 | CCCGACTCTACTAAA[A/T]ATACAAAAATTAGCC | 7874 |
rs139013909 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | USP7 | GRCh38.p7 | 16:8914342 | ACTGTGCAATTGATA[A/C]ACCACTTTGGGAATC | 7874 |
rs139025820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8944587 | CAAACAGGTTCCTTT[A/G]TTTGAATAAAACCAC | 7874 |
rs139050276 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8958730 | TCTAGCACTCACGCA[A/G]GAATCATCAGAAGGC | 7874 |
rs139058982 | snp | C/G | 0.00874735 | 0.0655527 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938682 | CACCACTGCACTCCA[C/G]CTTGGGTAACACAGC | 7874 |
rs139079836 | snp | A/G | 0.0287284 | 0.116357 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937316 | TTGGGAGGCTGAGGC[A/G]GGCGGATCACCTGAG | 7874 |
rs139102753 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8899220 | AAGGTTCACATTTTG[C/G]GGAAAAATTGAAACT | 7874 |
rs139136181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8927575 | CCTTGGTGGCTCACA[C/T]TTGTAGTCCCAGTAC | 7874 |
rs139138924 | in-del | -/ACAACAATGTGGGGGTTTGTAGTTGCATCATTTAA/ACAACGACGTGGGGGTTTGTAGTTGCATCATTTAA/ACAACGATGTGGGCGTTTGTAGTTGCATCATTTAA/ACAACGATGTGGGGGTTTGTAGTTACATCATTTAA/ACAACGATGTGGGGGTTTGTAGTTGCATCATTTAA/AGAACGATGTGGGGGTTTGTAGTTGCATCATTTAA | 0.0116017 | 0.0752941 | intron-variant | USP7 | GRCh38.p7 | 16:8923204 | TTCCAGTAATGAAAT[lengthTooLong]ACTGTCTTACGTGGA | 7874 |
rs139195208 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961179 | GAATTTCTAAAAATT[C/G]AACACCCTCTAGTCT | 7874 |
rs139207411 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8917980 | TATTTTTACTAGAGA[C/T]GGGGTTTCACCATGT | 7874 |
rs139207898 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP7 | GRCh38.p7 | 16:8903821 | GAGGTGAGCAGAGAT[C/T]GCGCCACTGCACTCA | 7874 |
rs139232336 | snp | A/G | 0.00330665 | 0.0405264 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8917070 | TACAGGTTTATCACT[A/G]TGCTGTAATTCATAG | 7874 |
rs139240720 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8911176 | CTCAAAAGCAGAGAT[A/G]CACAAATGTGAATGG | 7874 |
rs139344576 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | USP7 | GRCh38.p7 | 16:8913396 | AGGAGAGAAGAGAAG[A/T]GAAGTGAAGCGAAGC | 7874 |
rs139348494 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | USP7 | GRCh38.p7 | 16:8952304 | ACCAATAGCACTTAC[C/T]GGCTATGGTGAAGCC | 7874 |
rs139476709 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | USP7 | GRCh38.p7 | 16:8952540 | CCATTCCTGGGCTCC[C/G]CCTTGCACCTGTCTT | 7874 |
rs139520157 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | USP7 | GRCh38.p7 | 16:8922280 | GATCACCTGAGGTCA[A/G]GAGTTCGAGACCAGC | 7874 |
rs139555576 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | USP7 | GRCh38.p7 | 16:8948506 | TAACTCAACTTAGTA[A/C]GTGAAGCATATTCCT | 7874 |
rs139628004 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | USP7 | GRCh38.p7 | 16:8943537 | AGGGCCCCAATGCCA[C/T]GAGAAACACAAACGA | 7874 |
rs139676471 | snp | G/T | 0.00954511 | 0.0684907 | intron-variant | USP7 | GRCh38.p7 | 16:8929183 | AAACGCACACCTAGC[G/T]CCTCAGAGCTGGCCA | 7874 |
rs139676650 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8892879 | AAACAACCCAAAAAA[C/T]ACCGGAAAAGGATGA | 7874 |
rs139699734 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8917248 | TCATGTTTAAAAAAA[C/T]CATTTCTAATAACAC | 7874 |
rs139730767 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | USP7 | GRCh38.p7 | 16:8919947 | ACTCCTCGCTCACCA[C/T]GTTAGTTGTCGGTGA | 7874 |
rs139767926 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | USP7 | GRCh38.p7 | 16:8945700 | ATAGCTAAGGACAAG[C/G]TGATTCTAATATTTA | 7874 |
rs139769784 | snp | A/G/T | 0.000133631 | 0.00817306 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8920439 | TCCTTTCTCAGGATC[A/G/T]GTCACTTCCTATAAA | 7874 |
rs139793864 | snp | C/T | 0.00676609 | 0.0577691 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8965316 | TTTGGGAGGCCAAGG[C/T]GGGCGGATCACTTGA | 7874 |
rs139826487 | snp | C/T | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961927 | CCCCCATTACTGCCA[C/T]TGATAAATACCACTG | 7874 |
rs139865632 | snp | A/G | 0.040671 | 0.13668 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938466 | ACCTGTAATCCCAGC[A/G]CTGTAGGAGGCCGAG | 7874 |
rs139870777 | snp | C/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893520 | GCTATTTATTAGGTT[C/G]TGAGTTTCTCTGTTT | 7874 |
rs139916831 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8931913 | TGCACTGGACACCAA[C/G]AGAAATTAAGAATCT | 7874 |
rs139928102 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8915175 | GACTATTTAAAAAAA[C/T]ATCACTTGTGTAAAT | 7874 |
rs139939924 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | USP7 | GRCh38.p7 | 16:8929070 | AAGAAAAAAACAGTA[G/T]GGAAATGTTGGAACA | 7874 |
rs140041819 | snp | A/G | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8930366 | GATCACAGGGTTCTG[A/G]GTAATTCTTGGTGGG | 7874 |
rs140050804 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | USP7 | GRCh38.p7 | 16:8954442 | CTCATCATATGAGGC[A/G]TGACTGCATTCGGGT | 7874 |
rs140058679 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | USP7 | GRCh38.p7 | 16:8930631 | TACCACACTATAATT[G/T]GCTTTATTTGCAATG | 7874 |
rs140079504 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8948782 | GCATGGAAAACACAG[C/G/T]GAAACCCCGTCTCTA | 7874 |
rs140083650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8908083 | TCCTTGTGGACTTAA[A/G]TCAGCCATAGCTGAG | 7874 |
rs140135708 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894239 | CCAGGACCTGAGCTA[C/G]ACGCCCACCTGGAGC | 7874 |
rs140152394 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8940365 | GGTGAGCTCCAGCAC[A/G]GGACCAGCCTCCAGC | 7874 |
rs140154776 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8895976 | CGAGTAGTTGGGACT[A/G]CAGGTGCGTGCCACC | 7874 |
rs140196242 | snp | A/G | 0.00755907 | 0.0610114 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957800 | TAAAAACACAAAAAC[A/G]ATAACAAAAATAGAC | 7874 |
rs140228725 | in-del | -/A | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8951338 | CCTCTGGTAGCCCTG[-/A]GACCCAGTTTTCCTT | 7874 |
rs140316737 | snp | A/G/T | 0.000553606 | 0.0166295 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8902396 | TGTTTTATTGCCGTC[A/G/T]GCTTCATTATCTAAC | 7874 |
rs140318472 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8933472 | GTTGAAATAGAAATA[C/T]ATAATTTCATATTCC | 7874 |
rs140327428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8916155 | CACTGGAGTAACAAC[A/G]GAAGTCACCACTGTA | 7874 |
rs140337763 | snp | C/T | 1.6486e-05 | 0.00287102 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8897096 | CTGGATATAGTGTTA[C/T]TTCCTAAGTAATGAA | 7874 |
rs140404860 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | USP7 | GRCh38.p7 | 16:8935366 | AGGCACCTGCCATCA[C/T]GCCCAGCTAATTTGT | 7874 |
rs140478337 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | USP7 | GRCh38.p7 | 16:8922692 | GGGTTTTTGATAAAG[C/G]GTGAATTAATTTTCT | 7874 |
rs140481416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8925806 | GATGACACTTCGGGT[A/G]TATTAAAATTTCACC | 7874 |
rs140495897 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8943747 | ATTAAAATCAAAATG[A/T]TGAATGTCCTTTCAC | 7874 |
rs140531415 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | USP7 | GRCh38.p7 | 16:8928293 | TTCCCAGATTGTGTG[A/C]CCTAGTCTGAAATGG | 7874 |
rs140547336 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | USP7 | GRCh38.p7 | 16:8923720 | TCCCAAGGACCCCAG[C/G]CACCAAGTGAGTGGA | 7874 |
rs140589701 | in-del | -/AA/AAG/AG/G | 5.2603e-05 | 0.00512823 | intron-variant | USP7 | GRCh38.p7 | 16:8916985 | TACTCACTTGTCCTA[-/AA/AAG/AG/G]AAAAAAAAAAAAAAA | 7874 |
rs140617953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8896758 | CTTAATTGTGAAACA[C/T]GCATAACCCTCTGCA | 7874 |
rs140621825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8925026 | GTTTAAGATAATAAC[A/G]TCTAGAATGGCGTGG | 7874 |
rs140642785 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP7 | GRCh38.p7 | 16:8944759 | TCTCATGGAACACCT[A/G]CAATTCAAGGGCTGT | 7874 |
rs140671941 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | USP7 | GRCh38.p7 | 16:8912280 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 7874 |
rs140715885 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP7 | GRCh38.p7 | 16:8946567 | CTCAAATATATAAAC[A/G]ACAGTTCACAAAACT | 7874 |
rs140733225 | snp | C/T | 1.6476e-05 | 0.00287014 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8897022 | CCCTGATGCTTTCTC[C/T]CCAAGCTCCACGGCC | 7874 |
rs140744809 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP7 | GRCh38.p7 | 16:8918519 | TTTAAGTCTGCAAAA[C/T]TAGGTCATGGCTGGG | 7874 |
rs140760758 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | USP7 | GRCh38.p7 | 16:8913068 | AAACCTTAAAAGCAC[A/G]TGGGGGGCTGGGCAC | 7874 |
rs140761979 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8935146 | ATATGCCACCTTTTC[A/G]GAAGTTTTTAAGACA | 7874 |
rs140776174 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891637 | AGGAAGCGATGGTGT[C/G]TAGACGTGGCTTCTC | 7874 |
rs140810358 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | USP7 | GRCh38.p7 | 16:8913775 | TACTTTCTTGAGAGA[G/T]ATACTTGCTCTGTTG | 7874 |
rs140846417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8935673 | ATATCCCACTCAGAA[A/G]TAGAAGACAGTCTCC | 7874 |
rs140891749 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8932189 | AATACCAAGAAACAG[A/G]TATTACCACTCAGAC | 7874 |
rs140992704 | snp | C/G | 0.00150691 | 0.0274077 | intron-variant | USP7 | GRCh38.p7 | 16:8923445 | TCATCAGTCACAGAG[C/G]CTGTGCATTGACCAA | 7874 |
rs141022022 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | USP7 | GRCh38.p7 | 16:8949377 | GGGAAAAACTACTGT[A/T]CGAGGCATTGAAAAT | 7874 |
rs141030462 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | USP7 | GRCh38.p7 | 16:8911530 | AACGCAACTGCACAA[A/C]ACTGAAAACAGCGCT | 7874 |
rs141032462 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8934233 | ATCACATGTAAGTGT[A/G]AGCAGTCTAAAGTGT | 7874 |
rs141105453 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | USP7 | GRCh38.p7 | 16:8959192 | GGAGAAACTGAGGAA[C/T]CAAGAGCTTAAGCAA | 7874 |
rs141186736 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8946120 | CTACAGCCCCTCCCC[C/T]ACAAGACTCTCAACC | 7874 |
rs141192867 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | USP7 | GRCh38.p7 | 16:8905081 | GCTGTGAATACAATG[A/G]AATAAGCATAAAATG | 7874 |
rs141193525 | snp | C/T | 0.000198036 | 0.00994881 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8895687 | AGATAAACATTCTAA[C/T]AGTTCATCTTCTTGA | 7874 |
rs141198030 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP7 | GRCh38.p7 | 16:8923957 | AATGCTAACCTCATT[A/G]GTTCACGATTTTTGC | 7874 |
rs141217326 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8949845 | ATGCCCTAAGCTGAG[C/T]TTGGGGAAGCTCCTT | 7874 |
rs141233011 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8951909 | TGCCACCTGCAGTGT[A/C]TCAGTGGCCCTGGAC | 7874 |
rs141247794 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP7 | GRCh38.p7 | 16:8944488 | GGGACTGGGGATGAG[A/G]TCAGAGGTAGAAAGG | 7874 |
rs141253787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8901352 | AAGCTGAATAGCTCA[A/G]TGACAAGTGAAATGA | 7874 |
rs141341045 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | USP7 | GRCh38.p7 | 16:8927095 | CGGGGTGGGCGAGGC[A/G]AATCATGAGGTCAGG | 7874 |
rs141351426 | in-del | -/ACAACGATGTGGGGGTTTGTAGTTGCATCATTTAA | | | intron-variant | USP7 | GRCh38.p7 | 16:8923205 | TCCAGTAATGAAATA[lengthTooLong]CTGTCTTACGTGGAA | 7874 |
rs141361914 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | USP7 | GRCh38.p7 | 16:8941610 | GTTAGTCTGCCAATT[C/T]GCTTAGTATCTTCCT | 7874 |
rs141380736 | in-del | -/AT | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8925191 | TTTTACAAAGTGACA[-/AT]AGAGGATTTTAATAT | 7874 |
rs141390998 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | USP7 | GRCh38.p7 | 16:8931698 | AACAACATTCCAATC[A/C]CTTTTCATTAATTTT | 7874 |
rs141461904 | snp | A/C/G | 3.31583e-05 | 0.00407164 | intron-variant | USP7 | GRCh38.p7 | 16:8910843 | CTTTAAAGAGAGAGA[A/C/G]AGAAAAGTCAAGTGC | 7874 |
rs141526086 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960869 | TTTTTAAACCACACA[C/T]CAGTGGGTACTCACA | 7874 |
rs141538132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8898762 | ATTTGGACCTAGCAT[A/G]GGGTTTAACTTAATA | 7874 |
rs141622349 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8940403 | TCAGGAGAACTCTTC[G/T]GCTTCTTGAACACAA | 7874 |
rs141678236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8944845 | ACACAGTGGCTCATG[C/T]CTGTGATCCCAGCAC | 7874 |
rs141777914 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8948199 | GGAACCCTCAACTGA[C/T]CTTGATTCCTCCCTC | 7874 |
rs141778646 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | USP7 | GRCh38.p7 | 16:8953087 | TAATCTGTCGCCTTG[G/T]CCTCCCGAAATGCTG | 7874 |
rs141782199 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | USP7 | GRCh38.p7 | 16:8907061 | GAAGGCAAGTTAGAC[G/T]GGTGGGGGCTGGTCT | 7874 |
rs141788616 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8912082 | TATCTGTGCATAAGA[C/G]CAAAGGTTAGGAATA | 7874 |
rs141818560 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | USP7 | GRCh38.p7 | 16:8912692 | TTCGGGAGGCCAAGG[A/C]GGGCAGACTGATTGG | 7874 |
rs141851963 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | USP7 | GRCh38.p7 | 16:8912363 | AGGCTGAAAGGAGAA[C/T]TGCTTGAACCCAGGA | 7874 |
rs141856598 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | USP7 | GRCh38.p7 | 16:8919354 | CACAGCCCTCGAAGC[A/G]CCTGCCTGCTGACAG | 7874 |
rs141952247 | snp | A/G | 0.0103295 | 0.0711199 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937899 | CATCTATGTGGGAGC[A/G]AGAGGGGGAGAGAAA | 7874 |
rs142036589 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894161 | CCTGGAACCCCTCAG[C/T]GGGGTGGTGGCCAGT | 7874 |
rs142062834 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | USP7 | GRCh38.p7 | 16:8928425 | TTATGCTGCTTCTGA[A/T]ATGACAACCCTGAGA | 7874 |
rs142069320 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8920105 | AGCTGAGTGTACATT[C/G]TTTAGGAACAGAAAA | 7874 |
rs142135685 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | USP7 | GRCh38.p7 | 16:8955906 | TCCCTTGGAAACACA[C/T]CTCTCAACTTTTTCT | 7874 |
rs142143501 | snp | A/C | 6.58957e-05 | 0.00573964 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8894818 | TGGATGTCCAGCAGG[A/C]TCTGGATTCGCTTCA | 7874 |
rs142171017 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8942191 | TTAACTTCACTCTAA[A/G]ATGTTCCCTCCCAGC | 7874 |
rs142175890 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | USP7 | GRCh38.p7 | 16:8922720 | TCTAATTCATCTAAA[C/T]AGAAGGACCATCAAG | 7874 |
rs142200910 | snp | A/G | 0.000156308 | 0.0088391 | intron-variant | USP7 | GRCh38.p7 | 16:8921332 | GCCTTAGTTGACATT[A/G]TTTACCAGATGTTAT | 7874 |
rs142205911 | snp | C/T | 0.00795532 | 0.062565 | utr-variant-3-prime, nc-transcript-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8892248 | CTCGCACCCCTGCTC[C/T]AACTCCTCTTTCTGG | 7874 |
rs142244626 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8921744 | CTTGCTGTCCTGCCC[A/C]GGCATCGACGAATTC | 7874 |
rs142330340 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | USP7 | GRCh38.p7 | 16:8925642 | CCCCGCAGAGGCCAC[C/T]GCGCATCCGTCTCTG | 7874 |
rs142422494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8939916 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGACTC | 7874 |
rs142431583 | snp | C/T | 0.0119091 | 0.0762411 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964213 | CTGGGGAGCCGGACA[C/T]CCCGAAAGACCCAGG | 7874 |
rs142444518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8928174 | CTTTGTCTCATTAGC[C/T]ATTTAGCATCTTACA | 7874 |
rs142482171 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | USP7 | GRCh38.p7 | 16:8934511 | CATTTTTCAGCAGTG[A/G]GATTAATTGCAGTGT | 7874 |
rs142506935 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | USP7 | GRCh38.p7 | 16:8909111 | AACTTCTCAACAAGC[C/T]TTCTATGGGGACACC | 7874 |
rs142523677 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8896469 | AAGCCATTTGTCCTC[C/T]AAGCGACTACAGGGC | 7874 |
rs142571297 | snp | C/G/T | 0.0158469 | 0.0875917 | intron-variant | USP7 | GRCh38.p7 | 16:8905614 | TATAATCTACTGAAA[C/G/T]AGCCCATTTTCCACT | 7874 |
rs142575073 | snp | C/T | 0.000883399 | 0.0209981 | intron-variant | USP7 | GRCh38.p7 | 16:8930267 | AGTTTCCGCCCACTG[C/T]GAGGCGGTGAACCAC | 7874 |
rs142653424 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | USP7 | GRCh38.p7 | 16:8930921 | CTGCAGTGAGCCAAG[A/T]TCATGCCACTGCACT | 7874 |
rs142678397 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | USP7 | GRCh38.p7 | 16:8906358 | GAGTAGGAACCAGAA[C/G]AGGCTGAAGCAGAGC | 7874 |
rs142706172 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8945319 | TACCTGGGAGGTGGA[A/G]GTTGCAGTGAGCCAA | 7874 |
rs142712886 | snp | G/T | 0.000629765 | 0.0177337 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8903394 | ACAAAACTGGTCCTC[G/T]GCGACTATCTGAAAA | 7874 |
rs142838174 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | USP7 | GRCh38.p7 | 16:8929089 | AATGTTGGAACAGAT[C/T]GCTCTGTGGGAACTA | 7874 |
rs142869172 | snp | C/T | 0.000131981 | 0.00812237 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8900559 | GATGTCACCATCCAT[C/T]AGTTCATCAAGGGCT | 7874 |
rs142900210 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8915016 | TGTTAGAAGTCCACG[G/T]GGTGGTTTCCTGTGA | 7874 |
rs142915916 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | USP7 | GRCh38.p7 | 16:8895822 | TTTTCTAGAAAGAAA[G/T]AAAGTTACCACGATA | 7874 |
rs142952736 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960301 | CATCAGGCCCCACCT[C/G]TTCCCTCTCCGCACT | 7874 |
rs142960410 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8948990 | AAAGCTTACACAGTC[C/T]ATGAAATGTCTAGAA | 7874 |
rs142965851 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | USP7 | GRCh38.p7 | 16:8908803 | GCAAATTATGGAGAA[A/C]CACAGAAAAATCATT | 7874 |
rs142985705 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP7 | GRCh38.p7 | 16:8922017 | TGCTCGGGACGCTGA[C/T]ACTGGGTATGGACCA | 7874 |
rs143018958 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957031 | TCATCACTGAATTCT[A/G]GAAGCATCCCTGCTC | 7874 |
rs143024328 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | USP7 | GRCh38.p7 | 16:8914920 | TATCTCAAAAAACAA[C/G]AGCGAAATAAACAAA | 7874 |
rs143048965 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8941930 | TCATTGCAATAGAGG[A/G]CAAACGCACACAGTG | 7874 |
rs143056301 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8898280 | TTCTGTGGTGTCTTA[C/G]TTTTCAATGTCTGGG | 7874 |
rs143060841 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8947167 | GCTGACTGAATGCAC[A/T]AGCAGGTATGAAGTC | 7874 |
rs143088519 | snp | A/G | 8.23608e-05 | 0.00641667 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8895061 | CAAAAACGGGATTCC[A/G]AACGTTCCGAAGACC | 7874 |
rs143105472 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | USP7 | GRCh38.p7 | 16:8913544 | GAAGGAACCTGCCAA[A/C]CTAGAAGTCTACACC | 7874 |
rs143167626 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950807 | CAGGCACTGACCAGC[A/G]CACGACAGTGATCTG | 7874 |
rs143171655 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | USP7 | GRCh38.p7 | 16:8910043 | GTACACAGGCACCAT[G/T]AACTATATACACTGG | 7874 |
rs143172337 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8935165 | GTTTTTAAGACATGG[A/G/T]GACTGATTTGGCCAA | 7874 |
rs143180450 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8932628 | TTAAAAAAGAGAAAG[A/G]AAAGAAAAATCAGGT | 7874 |
rs143225074 | in-del | -/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937207 | CAGTGAGACTCTGTC[-/T]TTTTTTAAAAAAAAA | 7874 |
rs143313151 | snp | C/G | 9.89642e-05 | 0.00703365 | intron-variant | USP7 | GRCh38.p7 | 16:8895190 | GTTCTGTAAGTGCAA[C/G]TGATGTGGTCAAAGT | 7874 |
rs143315917 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938605 | TAGTCCCAGCTACTC[C/T]GGAGGCTGAGGCAGG | 7874 |
rs143342816 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | USP7 | GRCh38.p7 | 16:8923820 | ACGACATGGGACTTG[C/G]GCTGACTTTACAGAG | 7874 |
rs143380484 | snp | A/T | 0.0349115 | 0.127424 | intron-variant | USP7 | GRCh38.p7 | 16:8926710 | CCACATTCACTGCAA[A/T]ATTAGCACTTCATGC | 7874 |
rs143401802 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | USP7 | GRCh38.p7 | 16:8907627 | TTGGGAGGCTGAGGC[C/T]GGCAGATCACTTGAG | 7874 |
rs143424623 | in-del | -/CAGG | 0.0603597 | 0.1629 | intron-variant | USP7 | GRCh38.p7 | 16:8914398 | CATACGCACACCCTA[-/CAGG]CAGGCCAGTAATCCT | 7874 |
rs143438346 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8924916 | GCAGCTGAAAGAGGC[A/G]CATCTTGTCCAAAAT | 7874 |
rs143487274 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP7 | GRCh38.p7 | 16:8912090 | CATAAGAGCAAAGGT[C/T]AGGAATATCTAACAC | 7874 |
rs143553578 | snp | A/C | | | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962170 | CATTCATTGAGGCAA[A/C]CCAAGATCCCTTGCT | 7874 |
rs143589416 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP7 | GRCh38.p7 | 16:8928590 | TCAGCTACAAGTTCT[C/T]CTCCTACAGTCAGGA | 7874 |
rs143600902 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | USP7 | GRCh38.p7 | 16:8946226 | ACATCTGTCATGATG[C/G]GTAGGGCAAATATTT | 7874 |
rs143625911 | snp | G/T | 0.0460142 | 0.144533 | intron-variant | USP7 | GRCh38.p7 | 16:8935403 | TTTTGTAGAGATGGG[G/T]TTTCACCACGTTGGC | 7874 |
rs143655773 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | USP7 | GRCh38.p7 | 16:8941893 | GTGCTCACTAGGAAG[A/T]GGGAGGCAAGTCCCT | 7874 |
rs143746915 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP7 | GRCh38.p7 | 16:8948825 | AAAACTTAGCCAGGC[A/G]TGGTGGCGTGTGCCT | 7874 |
rs143765126 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8944824 | TGAAAAGTTCCTGGC[A/G]GCTGGACACAGTGGC | 7874 |
rs143770006 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8902845 | GTGAGCCAAGATCGC[A/G]CCACTGGGCAACAAG | 7874 |
rs143793947 | snp | C/T | 0.000341565 | 0.0130639 | utr-variant-5-prime, intron-variant | USP7 | GRCh38.p7 | 16:8936638 | GCTCTGCAGTGGCCT[C/T]TGCTGGGGGATGGGG | 7874 |
rs143818812 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP7 | GRCh38.p7 | 16:8917675 | AGAGCTACCGCACCC[A/G]GCCTCACCCATATGT | 7874 |
rs143858240 | snp | C/T | 0.000406587 | 0.0142523 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962500 | CAGGTTTGATTCTGA[C/T]GCAGGCAGCCATGTG | 7874 |
rs143858324 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | USP7 | GRCh38.p7 | 16:8933970 | CCATGTTGGCCAGGC[G/T]GGTCTCAAACTCATG | 7874 |
rs143955328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8918155 | TAAAAACTTAAATGT[A/G]ACTAGAATTACCCAT | 7874 |
rs143960693 | snp | A/G | 4.94197e-05 | 0.00497066 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8905311 | ACACCTTGACACCAC[A/G]TCGTCATCAAATTTA | 7874 |
rs143971123 | snp | C/G/T | 0.00795532 | 0.062565 | intron-variant | USP7 | GRCh38.p7 | 16:8919988 | TTCCCCCAGTCCCCC[C/G/T]TTCCTCACACTCGGA | 7874 |
rs143989939 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | USP7 | GRCh38.p7 | 16:8958916 | AGGCCGGATGGCTTC[C/T]TCCTAATCCACATCG | 7874 |
rs143996076 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8915944 | TCAATCCAGCTAGTG[A/C]TGCAAAAAAGAAAAC | 7874 |
rs144007527 | in-del | -/TT | 0.463881 | 0.12944 | intron-variant | USP7 | GRCh38.p7 | 16:8895840 | AGTTACCACGATATG[-/TT]TTTTTTTTTTTTTTT | 7874 |
rs144026244 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP7 | GRCh38.p7 | 16:8945740 | ATAAAAGATTGAGTA[A/G]GTAAAACAATTTTGA | 7874 |
rs144036205 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8904653 | CATCATTAATAAAAT[A/G]ATCTATTAGGCCGGC | 7874 |
rs144065481 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961355 | AAAGTAGCCAGGCGT[C/G]GTTGCACATGGCTGT | 7874 |
rs144078272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960396 | TGTTTTCCAATGAAT[A/G]TACAAGGACTGTGCA | 7874 |
rs144102588 | snp | G/T | 0.00139979 | 0.0264184 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8897006 | ATACTTGCCTAAGTT[G/T]CCCTGATGCTTTCTC | 7874 |
rs144116379 | snp | C/T | 0.000181185 | 0.00951628 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8923262 | GAATCCTACGCTTTT[C/T]TGGTGTGGTCTGTCT | 7874 |
rs144237905 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8917247 | TTCATGTTTAAAAAA[A/T]TCATTTCTAATAACA | 7874 |
rs144266553 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | USP7 | GRCh38.p7 | 16:8948685 | CTGGCTACGATGTGG[A/C]TGAACCTTGAGGATA | 7874 |
rs144266730 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | USP7 | GRCh38.p7 | 16:8931396 | TTTCACCATGTCGGT[C/G]AACTGGTCTCGAACT | 7874 |
rs144278404 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | USP7 | GRCh38.p7 | 16:8904725 | AGGCGGGCCGATCAC[A/G]AGGTCAGGAAATCAA | 7874 |
rs144343448 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP7 | GRCh38.p7 | 16:8927901 | TATAATCCCAACACA[C/T]TGGGAGGCCAAGGCA | 7874 |
rs144358776 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | USP7 | GRCh38.p7 | 16:8896812 | CTGAGACTTGAAAAA[C/G]TGGAGCAACACTGGG | 7874 |
rs144406562 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960604 | GTTCAGACCCTGACA[C/G]TTTCCAGCTGCTAGT | 7874 |
rs144410708 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8917451 | TGGCGCGACCTCAGC[A/T]CACTACAACCTCCGC | 7874 |
rs144430815 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893182 | CACTAGTGAGCATGC[C/T]CTCTTGCTAAAAGGC | 7874 |
rs144447086 | snp | A/C/T | 0.00260283 | 0.0359837 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8906447 | ATCCCCTTTGGGGTT[A/C/T]AGATAAACCACATAA | 7874 |
rs144492177 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8943032 | CAGTGGAGCCTGAGT[A/G]TTCAAAGTGGACCCA | 7874 |
rs144514369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8895984 | TGGGACTACAGGTGC[A/G]TGCCACCACACTGGG | 7874 |
rs144547509 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | USP7 | GRCh38.p7 | 16:8925342 | CCCGCTTTATGAAGC[A/C]CATGTATACAGAACT | 7874 |
rs144566601 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8941269 | GAAAAATTAACTATG[C/G]TCAAACATAACCCTG | 7874 |
rs144752536 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | USP7 | GRCh38.p7 | 16:8933667 | AATGTTGCCCAGGTT[G/T]GTCTTGAACTGGACT | 7874 |
rs144774845 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8911861 | GCAAGAGGATGAGGA[C/T]TGGGGGGAACAACCT | 7874 |
rs144851444 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | USP7 | GRCh38.p7 | 16:8933307 | TCCCAGCACTTGTGG[G/T]GGGCCAAGACGGGAC | 7874 |
rs144853998 | snp | A/G | 0.0399052 | 0.1355 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937435 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 7874 |
rs144861055 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892750 | GTAGAAATCTTCCTC[C/T]ACTTCCACGTAACTC | 7874 |
rs144910803 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8913098 | CGGTGGCTCACACCT[A/G]TAATCCCAAAATCTT | 7874 |
rs144915766 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | USP7 | GRCh38.p7 | 16:8959211 | GAGCTTAAGCAATGT[A/G]CATTAGGTCCCACAG | 7874 |
rs144927305 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8913463 | ACAGAAAGAGTAAGG[A/G]CACTACAGCCCACTT | 7874 |
rs145047119 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP7 | GRCh38.p7 | 16:8916014 | GTTGTGTGTGTGTGC[C/T]TCTGCGTCTTTTATC | 7874 |
rs145116305 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP7 | GRCh38.p7 | 16:8939837 | GAGCGCAGTGGCTCA[C/T]GCCTGTAATCACAGC | 7874 |
rs145148835 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | USP7 | GRCh38.p7 | 16:8944543 | GTGCTAATGTAAGTC[C/T]TTTAAAAATAGTCAA | 7874 |
rs145151865 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP7 | GRCh38.p7 | 16:8901411 | GATGTGGCTTATTCA[C/T]GAAGCTGAGGCTATT | 7874 |
rs145178564 | in-del | -/A | 0.00795532 | 0.062565 | intron-variant | USP7 | GRCh38.p7 | 16:8895905 | CAACAGCATGGTCTC[-/A]AGCTCACTGCAACCT | 7874 |
rs145182248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8941986 | CTTAGTCATGAAGGA[A/G]GAGACAACTGGCAAG | 7874 |
rs145183843 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | USP7 | GRCh38.p7 | 16:8944345 | GAGGCCAGAGTCCTG[C/G]AACAAAGGAATTGCC | 7874 |
rs145185787 | snp | A/G | 0.00108665 | 0.0232839 | intron-variant | USP7 | GRCh38.p7 | 16:8898678 | ATAAATGACTTGTTT[A/G]TTTGCCTAAAAACAA | 7874 |
rs145242233 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | USP7 | GRCh38.p7 | 16:8943657 | AGTACTGAAGGTCTA[C/G]CATATGGGTAGAGTC | 7874 |
rs145265695 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8921561 | AAATTTTCTTTCATT[G/T]TATCTATACAATTTT | 7874 |
rs145287047 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | USP7 | GRCh38.p7 | 16:8922580 | CCACTCTGTGGCGTG[G/T]CAGGGAGACTAGGAC | 7874 |
rs145302662 | in-del | -/AACGATGTGGGGGTTTGTAGTTGCATCATTTAAAC | | | intron-variant | USP7 | GRCh38.p7 | 16:8923172 | GATAAAATTGCACTA[lengthTooLong]GGCTGATCAAATTTG | 7874 |
rs145320568 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8920834 | AGCCAAAGTGAACTG[A/C]ATGATTACTGGAGTC | 7874 |
rs145324064 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8947114 | AGTATATCTCTGTAA[C/G]ATTGGTTTTTTCATA | 7874 |
rs145523052 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8956114 | TTAGTACATAACACA[G/T]GACACTGTCCTCCCA | 7874 |
rs145533706 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8913643 | ATCTCAGCCGACCCG[A/C]ACTAAATGATTCCTA | 7874 |
rs145567651 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP7 | GRCh38.p7 | 16:8954644 | TTACTAACTAAATAC[A/G]AAGGTATGTATTCAT | 7874 |
rs145585318 | snp | C/T | 0.000232802 | 0.0107864 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8902441 | TGTTCCATTACTCCT[C/T]GCTTGCATGGGCCAC | 7874 |
rs145596858 | snp | A/G | 0.00835141 | 0.0640778 | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891824 | AGGGCCACTGTGACC[A/G]CAGGCCCTTGCTGTC | 7874 |
rs145638450 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8962047 | TTATTCTATTCAGAG[A/G]TGAACACCAGTCACG | 7874 |
rs145646004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8897517 | TTTATGTCTCGAATT[C/T]TCCCTCTATACTTGT | 7874 |
rs145647422 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | USP7 | GRCh38.p7 | 16:8932023 | ATCCGAACCAGCAAG[C/T]AATCTGATTCAGCAC | 7874 |
rs145648364 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | USP7 | GRCh38.p7 | 16:8918732 | GAGAATCACTTGAAC[C/T]CAGGAGACAGAGGCT | 7874 |
rs145700538 | snp | A/G | 3.39876e-05 | 0.00412221 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8898636 | ACCTGGGCCATCCCT[A/G]TAACTACACAAGAAA | 7874 |
rs145706461 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | USP7 | GRCh38.p7 | 16:8908201 | TTTAACACTGCGGCT[C/G]TTGGGACACAGAGGT | 7874 |
rs145714242 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | USP7 | GRCh38.p7 | 16:8929793 | GTATGCTTTCTCACA[C/G]AGAAGCTATAGACCA | 7874 |
rs145714548 | snp | A/G | 0.00557542 | 0.0525036 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957973 | TATCAAAGCAATACC[A/G]TTTTATGGCTTCAGC | 7874 |
rs145741784 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | USP7 | GRCh38.p7 | 16:8900763 | TTAAAATGTTAACAG[C/G]AAAAGCTAAATGAAT | 7874 |
rs145769115 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8941810 | CCCTTCCAAGCCTCC[A/G]TCTCTGACAGATGGG | 7874 |
rs145775303 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | USP7 | GRCh38.p7 | 16:8897307 | GACCAACCAAATACT[C/G]ACGGGAGGTTAACAA | 7874 |
rs145846238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8929305 | CCACACCATTGCCCT[C/T]GTCTACGGTGGAAAG | 7874 |
rs145904392 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8928543 | GAAGAAGAGGATTGC[A/G]CAATTTGTACTGCAG | 7874 |
rs145917773 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8921783 | GCACAAAATTACAAC[C/T]ACAAGAGAACTACTG | 7874 |
rs145949182 | in-del | -/AC | | | intron-variant | USP7 | GRCh38.p7 | 16:8947357 | GCACTCCCCCCCCCA[-/AC]ACACACACACACAGG | 7874 |
rs145956568 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938258 | GCTACTACACTATAC[C/T]ATACTGACTTGATTA | 7874 |
rs145960641 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893273 | TGAACTGTTGAGATC[A/G]TAAGTCTGCCAAGGC | 7874 |
rs145973140 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP7 | GRCh38.p7 | 16:8939875 | GAGGCCAAGGAGGGC[A/G]GATCACGAGGTCAGG | 7874 |
rs145975438 | snp | C/T | 0.0134861 | 0.0810011 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964612 | CAAAGGTTTTGGGTT[C/T]TGTTTTTATATTTTT | 7874 |
rs145993314 | snp | A/G | 0.00256688 | 0.0357331 | intron-variant | USP7 | GRCh38.p7 | 16:8894869 | CCCTAGAATGGCAAA[A/G]GACATGTGCTCACAC | 7874 |
rs146082132 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | USP7 | GRCh38.p7 | 16:8907687 | TCTCTACTAAAAATA[A/C]AAAAATTAGCCAGGT | 7874 |
rs146083656 | snp | C/G | 3.295e-05 | 0.00405881 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8919115 | CTTTAAGCCGACGTA[C/G]CCTGTGTGCTTCTTT | 7874 |
rs146121535 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | USP7 | GRCh38.p7 | 16:8940293 | AGCTAACCATGCTTT[A/G]TCCAATGGCAAATGT | 7874 |
rs146124017 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP7 | GRCh38.p7 | 16:8895974 | CCCGAGTAGTTGGGA[C/T]TACAGGTGCGTGCCA | 7874 |
rs146202746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8942463 | ACCTCACCCCAGCCT[A/G]TCAAAGTAGATCCCT | 7874 |
rs146222398 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8940438 | AGGCAGAAGGTGTAC[C/T]AGGAATGTCCAAGAA | 7874 |
rs146242113 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | USP7 | GRCh38.p7 | 16:8951935 | TGGACTATTCAGGCA[G/T]TGGGCTACTTTCTAT | 7874 |
rs146244978 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP7 | GRCh38.p7 | 16:8910545 | GCTGGATGTGCTTCT[A/G]CAGGATAAACCAGCT | 7874 |
rs146339105 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP7 | GRCh38.p7 | 16:8952539 | CCCATTCCTGGGCTC[C/T]CCCTTGCACCTGTCT | 7874 |
rs146365980 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8919795 | ACGACCTGAACACAC[A/G]ACCGTCACCAAGCGG | 7874 |
rs146417442 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961896 | CCAGTCCTTGGCGTG[A/G]ACTCCGCTCTTCTGT | 7874 |
rs146438179 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | USP7 | GRCh38.p7 | 16:8959033 | GTGTCACATTTTCTT[C/G]GCTGCAAAAGCCCTA | 7874 |
rs146459497 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8935042 | GCCTAAACGATAAGG[C/T]TGCCTTCTTTTATTG | 7874 |
rs146480699 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8923274 | TTTTTGGTGTGGTCT[A/G]TCTGGATAAAAGCGT | 7874 |
rs146496592 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8941651 | TGTAGCCTTGCTTGG[C/T]ACCAGGAAAGACAAA | 7874 |
rs146496797 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8916227 | TTGGTTTCTGGATTA[A/G]TAACTCCTGTATATA | 7874 |
rs146507622 | snp | C/T | 0.000131835 | 0.00811788 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8903304 | AACAAACTCAGCAAG[C/T]GAGGAGTTCTTCAAT | 7874 |
rs146543831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8928064 | AAGTAGAATGAGTAG[A/G]TACAGTAAAAGATAA | 7874 |
rs146544605 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | USP7 | GRCh38.p7 | 16:8900886 | GAGGCCCTGAGTTAG[C/G]TGGTAGACCTAACAC | 7874 |
rs146591816 | in-del | -/AG | 0.0138799 | 0.0821421 | intron-variant | USP7 | GRCh38.p7 | 16:8912473 | AAAAAGAAAGAAAAA[-/AG]AAAATAAACATTACC | 7874 |
rs146621571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8939932 | GTGAAACCCCGACTC[C/T]ACTAAAAATACAAAA | 7874 |
rs146622308 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | USP7 | GRCh38.p7 | 16:8925946 | GATCACGAGGTCAGG[A/T]GATCGAGACCATCCT | 7874 |
rs146663534 | snp | A/G | 0.00914312 | 0.0669923 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938627 | TGAGGCAGGAGAATG[A/G]CATGAACCTGGGAAG | 7874 |
rs146663602 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8913568 | CTACACCGAGTTAAA[A/C]TGTCTTTCACAACTG | 7874 |
rs146728439 | snp | C/T | 1.65132e-05 | 0.00287339 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8901044 | TCTGTCACACATAAC[C/T]GGGAGCAAGTCACCT | 7874 |
rs146741185 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | USP7 | GRCh38.p7 | 16:8935315 | CCTGGGTTCAAGTGA[G/T]TCTCCCACCTCAGCC | 7874 |
rs146784688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8923682 | TCCACATGAGAACAA[C/T]GTCTACTTTACTAAA | 7874 |
rs146784793 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | USP7 | GRCh38.p7 | 16:8948833 | GCCAGGCGTGGTGGC[A/G]TGTGCCTGCAGTTCC | 7874 |
rs146792298 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8909212 | GGCTTTGCCTATCTC[C/G]ACCACGGCCAGGCGG | 7874 |
rs146811907 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8932627 | TTTAAAAAAGAGAAA[A/G]AAAAGAAAAATCAGG | 7874 |
rs146864218 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | USP7 | GRCh38.p7 | 16:8946319 | GCGGCGGTGGCTTAA[C/G]CCGGTAATCCCAGCA | 7874 |
rs146881670 | in-del | -/CAAA | 0.00398564 | 0.0444627 | intron-variant | USP7 | GRCh38.p7 | 16:8935592 | GACTATGTGCAATGT[-/CAAA]CAGACAAGCCCTGGA | 7874 |
rs146929431 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | USP7 | GRCh38.p7 | 16:8947294 | TTACTTGGAAAATAA[G/T]TATTTTTTATACAAC | 7874 |
rs146945749 | snp | A/C | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8905242 | AGTGCAGTGTCGAAC[A/C]GACAGGTCGTCATCG | 7874 |
rs146949144 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | USP7 | GRCh38.p7 | 16:8926435 | ACTGAGCTGAGATCA[C/T]GGCATTGCACTCCAG | 7874 |
rs146962536 | snp | C/G | 4.95765e-05 | 0.00497853 | missense, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8930367 | ATCACAGGGTTCTGA[C/G]TAATTCTTGGTGGGT | 7874 |
rs146965968 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8949885 | TATTACATGAAAATG[C/T]TTGGCTTTCCATATT | 7874 |
rs147036040 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960312 | ACCTCTTCCCTCTCC[G/T]CACTTCACCCTTCAT | 7874 |
rs147057022 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892293 | AAGGGCCAGGTCCGC[A/G]GGGACCCTCACTCCC | 7874 |
rs147071274 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962272 | TCGTCACGTAGGTAA[A/G]AAAACTTTTTAAAGA | 7874 |
rs147091385 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | USP7 | GRCh38.p7 | 16:8928347 | GACACTCAAAAAAAG[C/G]GGGAGCTCTGAAGTC | 7874 |
rs147140392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8899349 | CCTTAATGAATCACC[A/G]TGGGAGTAGCATATC | 7874 |
rs147141621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8926849 | GTGTCACCACAAATC[C/T]TCAACCAGATTCCTT | 7874 |
rs147176623 | snp | C/G/T | 0.0044713 | 0.0470714 | intron-variant | USP7 | GRCh38.p7 | 16:8903236 | GGACGTTGGGAGCCA[C/G/T]GGTGGGGTATATCCA | 7874 |
rs147210739 | snp | A/G/T | 0.00478085 | 0.0486577 | intron-variant | USP7 | GRCh38.p7 | 16:8924988 | CTTTTGAGGATAGAA[A/G/T]TCTACTAAAAGGCAA | 7874 |
rs147215511 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937213 | GACTCTGTCTTTTTT[A/T]AAAAAAAAAAGGATT | 7874 |
rs147246477 | snp | C/G | 0.0031878 | 0.0397962 | utr-variant-5-prime, intron-variant | USP7 | GRCh38.p7 | 16:8936662 | GATGGGGGAGGTTCT[C/G]TCACCCACATCAGAG | 7874 |
rs147283264 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | USP7 | GRCh38.p7 | 16:8914296 | TCCAGTGTGGGTGTG[C/G]AGCAACTGCAACTCT | 7874 |
rs147329800 | snp | C/G/T | 9.91365e-05 | 0.00703985 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8906427 | GTCCCACCACTTACT[C/G/T]TGCCATCCCCTTTGG | 7874 |
rs147333649 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8932115 | TACATCATAAACCTC[A/T]CCAATAATTCCTGAA | 7874 |
rs147387024 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8924528 | ATCCCTGACCACCAG[C/G]CTCCTAAGGCACAAA | 7874 |
rs147436937 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8943397 | ACTGTGCAGCACAAT[A/G]CAAGTAGAAGTTGCA | 7874 |