SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs147458661 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP7 | GRCh38.p7 | 16:8916890 | ATAAAAGCACTGACA[C/T]GATTAAATGCTCAAG | 7874 |
rs147523234 | snp | C/T | 1.66252e-05 | 0.00288311 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8895721 | ACACCAATGATTTTG[C/T]AGCTTACAATTTCTA | 7874 |
rs147527788 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8914944 | AAACAAACAAATACA[A/T]CCTACTACAAGGTTC | 7874 |
rs147541426 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP7 | GRCh38.p7 | 16:8954253 | GACACGTGCCCCCTG[C/T]GGTGCCACTGGAAGC | 7874 |
rs147593249 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | USP7 | GRCh38.p7 | 16:8953203 | AGGCTCCCCCTCCCC[A/G]CGGTAAGCCAGTCCT | 7874 |
rs147648005 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | USP7 | GRCh38.p7 | 16:8922642 | TTCCAACTGCAGACA[A/G]GTTGACAAAGTGGTC | 7874 |
rs147649202 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8894717 | TGGCAAAAAAGCCTA[A/C/G]GCCGCTACGCTAGGC | 7874 |
rs147674955 | in-del | -/T | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960736 | TTCCAGCCTTCTGGC[-/T]TTTTTAACAGAAGTG | 7874 |
rs147681425 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | USP7 | GRCh38.p7 | 16:8939898 | AGGTCAGGAGATTGA[A/G]ACCATCCTGGCTAAC | 7874 |
rs147717614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8930186 | CCTGAAAACTAGCTA[C/T]GCTCAGAAGTACCCA | 7874 |
rs147736032 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | USP7 | GRCh38.p7 | 16:8911492 | TGTATGGAGAGCTCG[C/T]CCTGCTCCGGTCATG | 7874 |
rs147819901 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP7 | GRCh38.p7 | 16:8941406 | AGAAAACATCTTATT[C/T]TGTAGCCTAATACGT | 7874 |
rs147822927 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8896927 | GGTGATTTCCACCAA[C/T]GCAACTGCAGAGGTC | 7874 |
rs147858837 | snp | C/G | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8900220 | TGAATTACCCAAGTA[C/G]GTACATTCTAAGGAG | 7874 |
rs147891455 | snp | A/C/T | 0.00337831 | 0.040973 | intron-variant | USP7 | GRCh38.p7 | 16:8919173 | GTTGAGGGGATCTTG[A/C/T]AGATACCCCATTGCT | 7874 |
rs147925472 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | USP7 | GRCh38.p7 | 16:8952977 | AAGTAGCTGGGATTA[C/T]AGTCGCGTGTCACCA | 7874 |
rs147964623 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | USP7 | GRCh38.p7 | 16:8913314 | TGAGCCGAGATCGCA[C/G]CACTGCACTCCAGCC | 7874 |
rs147994518 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP7 | GRCh38.p7 | 16:8902873 | AAGAGTGAAACTCTG[C/T]CTCAAAAAAAAAGAA | 7874 |
rs148030528 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | USP7 | GRCh38.p7 | 16:8935508 | GGGCCACCATGCCCA[A/G]GCTATGGCACTATTT | 7874 |
rs148047988 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8906749 | CCGTACTTGATAGAA[A/G]TAACTATTCCTAGTC | 7874 |
rs148064637 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | USP7 | GRCh38.p7 | 16:8928746 | TTTTTCCATCAAGGA[C/G]GTCACAAGAAGGGCA | 7874 |
rs148081930 | in-del | -/T | 0.0759472 | 0.179459 | intron-variant | USP7 | GRCh38.p7 | 16:8924027 | TTTTAAGAACTGGTA[-/T]TTTTTTCCCACATGA | 7874 |
rs148082056 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8919317 | AGTGTGTGAACTGGT[A/G]CAAATGCAACCCCCA | 7874 |
rs148153003 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP7 | GRCh38.p7 | 16:8944839 | GGCTGGACACAGTGG[C/T]TCATGCCTGTGATCC | 7874 |
rs148206617 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP7 | GRCh38.p7 | 16:8926996 | CAGGGCAAAGGCCAA[C/T]AGACCAGCCTGGGCT | 7874 |
rs148244054 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | USP7 | GRCh38.p7 | 16:8916094 | AGTAATCACCGCATG[C/G]TGAGGTCTGCTCAAT | 7874 |
rs148276169 | snp | A/C/G | 0.00756529 | 0.0611122 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8951563 | ATCTGTAAATGCAGA[A/C/G]GGCTTGTGGGCATGA | 7874 |
rs148295997 | snp | C/G | 0.000874176 | 0.0208884 | intron-variant | USP7 | GRCh38.p7 | 16:8895200 | TGCAAGTGATGTGGT[C/G]AAAGTGTCCACATCT | 7874 |
rs148347100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8898753 | GGTCTTGAAATTTGG[A/G]CCTAGCATGGGGTTT | 7874 |
rs148362610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8923941 | CAGTAGCCTGATAAT[A/G]AATGCTAACCTCATT | 7874 |
rs148397533 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8895998 | CGTGCCACCACACTG[A/G]GCTGATTTTTGCATT | 7874 |
rs148449472 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8900300 | TAATAGTTGCCACGT[A/G]CACTTGAGACATTTT | 7874 |
rs148541392 | snp | C/T | 4.94279e-05 | 0.00497107 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8899628 | ATTCATTCTATTTGA[C/T]AACGTAACCACAAAT | 7874 |
rs148552453 | snp | A/G | 0.00874735 | 0.0655527 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937843 | GAGACAACTGGACAA[A/G]AGAATTGCTCAGGAG | 7874 |
rs148604379 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | USP7 | GRCh38.p7 | 16:8920056 | AGCATCTCTGCTCTG[C/G]GTATTTATGTACCGG | 7874 |
rs148620530 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | USP7 | GRCh38.p7 | 16:8942991 | CACTGCGGGCCCTGA[A/G]GTCAGCCGACCACCT | 7874 |
rs148644082 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | USP7 | GRCh38.p7 | 16:8928883 | TCCCCAGGAGACACC[C/T]GGCAATGTCTAGAGA | 7874 |
rs148672829 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8945882 | ATAGCGAGACCCCAC[C/T]TCCAAAAAAAAAGTA | 7874 |
rs148725870 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8928077 | AGATACAGTAAAAGA[C/T]AATTCTGATACTTGC | 7874 |
rs148745573 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8931457 | CTCCCAAAGTGCTGG[C/G]ATCACCCACCCATGC | 7874 |
rs148763840 | snp | C/G/T | 0.0115224 | 0.075102 | intron-variant | USP7 | GRCh38.p7 | 16:8917661 | TGGGATTATAGGCGA[C/G/T]AGCTACCGCACCCAG | 7874 |
rs148849549 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | USP7 | GRCh38.p7 | 16:8932395 | ACATAGTGAGACCTC[A/C]TCTCAATTTATTATT | 7874 |
rs148866380 | snp | A/G | 0.0256215 | 0.110247 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8962113 | ACACTTGGAGCCACC[A/G]CACAGGACAAATACT | 7874 |
rs148903877 | snp | A/T | 0.0103295 | 0.0711199 | downstream-variant-500B, nc-transcript-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8892052 | GTAACTGCGAGTGAG[A/T]GGAAAAGGGAACGCG | 7874 |
rs148917734 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | USP7 | GRCh38.p7 | 16:8941838 | GGGCTGGGCCCAGGG[C/T]TCGGCAGGGAACTGG | 7874 |
rs148921696 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8897310 | CAACCAAATACTGAC[A/C/G]GGAGGTTAACAAAAG | 7874 |
rs148938991 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | USP7 | GRCh38.p7 | 16:8908513 | CTGGAAGCAATGAAA[C/G]CAACAGCGGTTCAGC | 7874 |
rs148987704 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | USP7 | GRCh38.p7 | 16:8926369 | CTGTAATCCCAGCTA[C/G]TTGGGAGGTCGAGGC | 7874 |
rs149059159 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | USP7 | GRCh38.p7 | 16:8955571 | ATTAGCCGGGCATGG[C/T]GGCGCGCCCCTGTAG | 7874 |
rs149060714 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8913516 | AGACGGTAGAACGTC[C/T]AACAGACCGAAGGAA | 7874 |
rs149076974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8939851 | ACGCCTGTAATCACA[A/G]CACTTTGGGAGGCCA | 7874 |
rs149112417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8916046 | CAACTGGAAGAATGA[A/G]GATTTGCTAGTGATT | 7874 |
rs149125025 | snp | A/G | 0.00042823 | 0.0146264 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8923337 | CACAAAACACGGAGG[A/G]CTAAGGACCGACTCA | 7874 |
rs149129944 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | USP7 | GRCh38.p7 | 16:8921634 | TTGCTCCTGCCCCTA[C/G]AGCCCTTCAGTGCCA | 7874 |
rs149164873 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8894955 | TAACCCCAGCAGGAG[C/T]GCAGATTCGGCAACA | 7874 |
rs149180632 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP7 | GRCh38.p7 | 16:8923819 | CACGACATGGGACTT[A/G]GGCTGACTTTACAGA | 7874 |
rs149197080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8947116 | TATATCTCTGTAAGA[C/T]TGGTTTTTTCATATT | 7874 |
rs149232403 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8922452 | AAGATCAGGCCACTG[C/T]ACTCCAGCCTGGCGA | 7874 |
rs149252634 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | USP7 | GRCh38.p7 | 16:8928568 | CTGCAGCTGGAAAAC[A/G]CTGCCCTCAGCTACA | 7874 |
rs149269124 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | USP7 | GRCh38.p7 | 16:8895983 | TTGGGACTACAGGTG[C/T]GTGCCACCACACTGG | 7874 |
rs149281364 | snp | A/G | 0.00110343 | 0.0234627 | synonymous-codon, intron-variant | USP7 | GRCh38.p7 | 16:8904537 | CTGCTGAGGAATATC[A/G]TGGTCGGTGACCGCC | 7874 |
rs149302570 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | USP7 | GRCh38.p7 | 16:8948678 | ACGACTACTGGCTAC[C/G]ATGTGGATGAACCTT | 7874 |
rs149375139 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8933654 | GACAAGATTTTACAA[C/T]GTTGCCCAGGTTGGT | 7874 |
rs149429512 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892742 | CAGGGAGAGTAGAAA[C/T]CTTCCTCCACTTCCA | 7874 |
rs149443314 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962953 | TTACAACTCAGGGCG[C/T]TTTGTGCCGCGGAGG | 7874 |
rs149447581 | snp | C/T | 0.0029949 | 0.0385808 | intron-variant | USP7 | GRCh38.p7 | 16:8899229 | ATTTTGGGGAAAAAT[C/T]GAAACTTGGTCATAA | 7874 |
rs149464042 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950381 | TAAGAAAAATAAAAG[C/T]CCTTTAATTTCATCA | 7874 |
rs149465351 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | USP7 | GRCh38.p7 | 16:8909883 | GTGAGTCGAGATCGC[A/G]CCACTGCACTCTAGC | 7874 |
rs149638695 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8917423 | TCACTCTGTTGGCCA[C/G]GCTGAAGTGCAGTGG | 7874 |
rs149670898 | snp | C/G | 0.00874735 | 0.0655527 | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891640 | AAGCGATGGTGTCTA[C/G]ACGTGGCTTCTCGCC | 7874 |
rs149687118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8958401 | GCTGTGCGACTTCCT[A/G]TAGAGAAGGCAGGAC | 7874 |
rs149707450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8925038 | AACGTCTAGAATGGC[A/G]TGGTGGAATAAGTTT | 7874 |
rs149737412 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961973 | AGAATCCCAGCCACT[C/T]TGTCATTTGCAACCT | 7874 |
rs149741301 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | USP7 | GRCh38.p7 | 16:8918719 | GAGGCTGAGGCCAGA[C/G]AATCACTTGAACCCA | 7874 |
rs149762557 | snp | C/T | 0.0001812 | 0.00951667 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8897070 | CAGGTCCCGGACACA[C/T]CCATGCTTGTCTGGA | 7874 |
rs149829285 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | USP7 | GRCh38.p7 | 16:8932288 | AAGTTATTTCTGGTC[C/T]GACCCGTGGCTCACT | 7874 |
rs149898793 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | USP7 | GRCh38.p7 | 16:8934951 | TAAGACATGGTAAAT[A/C]CCTAGTCCAGAAGTA | 7874 |
rs149920185 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8904023 | TTGAAGCAACCTGAC[C/G]TGCACTTAATCACTT | 7874 |
rs149936865 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | USP7 | GRCh38.p7 | 16:8927582 | GGCTCACACTTGTAG[A/T]CCCAGTACTTTGGGA | 7874 |
rs149952289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8939181 | GTAGATTTGTGTGTC[C/T]ACTACCACCACAGTT | 7874 |
rs149953957 | snp | A/G | 6.64905e-05 | 0.00576548 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8894551 | GGGAGAACCCTTACC[A/G]GGCTGTGGCTCAAAG | 7874 |
rs149965411 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | USP7 | GRCh38.p7 | 16:8908098 | ATCAGCCATAGCTGA[C/G]AGCAGGGCTGGGACT | 7874 |
rs149985766 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8952546 | CTGGGCTCCCCCTTG[C/G]ACCTGTCTTCTCAGG | 7874 |
rs150010605 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8917121 | AGGGACGCTTTTAGA[C/T]GAATCATCCCCCTCG | 7874 |
rs150019824 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | USP7 | GRCh38.p7 | 16:8944018 | AGTTCAAGACCAGCC[G/T]GGGCAAACATAGGGA | 7874 |
rs150040209 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP7 | GRCh38.p7 | 16:8913462 | AACAGAAAGAGTAAG[A/G]ACACTACAGCCCACT | 7874 |
rs150090945 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | USP7 | GRCh38.p7 | 16:8912281 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATG | 7874 |
rs150096079 | snp | A/T | 1.64944e-05 | 0.00287175 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8903371 | TACATGTCATTCCCT[A/T]GGTGGCCACAAAACT | 7874 |
rs150142638 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP7 | GRCh38.p7 | 16:8913906 | GGTGCATGCCACCAC[A/G]CCCAGCTAATTTGTA | 7874 |
rs150209744 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8960078 | GAGTATTCAGAGGGC[A/G]GAGACCCATGCAAGT | 7874 |
rs150214934 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8897241 | CTCATTCCCACCCCA[A/C]CTCCCTCATCTGTGA | 7874 |
rs150245874 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | USP7 | GRCh38.p7 | 16:8949528 | TATTTTCATCCACCC[A/G]GAAGCCTTGCCGCTG | 7874 |
rs150262523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962553 | CAAGCGCACACCTGG[C/T]CGGATGCTGGCTGCA | 7874 |
rs150281325 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | USP7 | GRCh38.p7 | 16:8926061 | AGGGAGGCTGAGGCA[C/G]GAGAATGGCGTGAAC | 7874 |
rs150297856 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | USP7 | GRCh38.p7 | 16:8930668 | TGCACAAAACTTTTT[A/C]TATAAAATCTCTTAT | 7874 |
rs150334425 | snp | A/C | 0.0383715 | 0.133092 | intron-variant | USP7 | GRCh38.p7 | 16:8909765 | ACCCCATCTCTACTA[A/C]AAATACAAAAATTAG | 7874 |
rs150351455 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | USP7 | GRCh38.p7 | 16:8933548 | AGAACCTACTAGAGA[C/T]TAGGGTTACATAGAA | 7874 |
rs150422552 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8921423 | CTCCTTTCGGGTTGG[C/G]GTTAAAGGTAGGATG | 7874 |
rs150473108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8940042 | GGCGAAGGTTGTAGT[A/G]AGCTGAGATCATGCC | 7874 |
rs150494104 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | USP7 | GRCh38.p7 | 16:8946762 | CTCAACCACTCAGCC[A/G]TCTGCCAGCACGCAG | 7874 |
rs150494889 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | USP7 | GRCh38.p7 | 16:8905522 | CTCAGGCATCCGCTC[A/C]TACAATTCACCAGGA | 7874 |
rs150527015 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8922217 | AGTACGGCCAGGTGC[C/G]CTGGCTCACGCCTGT | 7874 |
rs150543187 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8945105 | AAATAAAAATACAGA[A/T]ATTAGCTGGGTGTGG | 7874 |
rs150596869 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8948480 | ATCAGCTGCCACACC[C/T]GGCCCCCAGTTAACT | 7874 |
rs150647814 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP7 | GRCh38.p7 | 16:8929122 | CCCGGAATGTTCCGA[C/T]AGGGCAGGGCCTGTC | 7874 |
rs150664676 | snp | C/T | 0.00676609 | 0.0577691 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957988 | GTTTTATGGCTTCAG[C/T]GTCTCTTTCTCAGAG | 7874 |
rs150666810 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8915139 | CTGTTTGCTTAAGAT[A/C]TGAGCCATTCTCTGT | 7874 |
rs150732455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961010 | AAGGAATCAGCATTA[A/G]TAACTAAAACCTCTG | 7874 |
rs150790252 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP7 | GRCh38.p7 | 16:8903608 | CTGTGGGCAGGGCAC[A/G]GTGGCTCATGCACTT | 7874 |
rs150807372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8927541 | TAGATCTTCAGAGGC[C/T]GTATTTGCTCTAAAA | 7874 |
rs150824614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8931904 | TTTCCCTGGTGCACT[A/G]GACACCAACAGAAAT | 7874 |
rs150837079 | snp | A/G | 0.00021418 | 0.0103462 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8915457 | TACCACCATTTTGCC[A/G]CGGAATAATTTGGGT | 7874 |
rs150875449 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | USP7 | GRCh38.p7 | 16:8934519 | AGCAGTGGGATTAAT[G/T]GCAGTGTGATGACTA | 7874 |
rs150926900 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP7 | GRCh38.p7 | 16:8932674 | TCATCCACATTCATT[C/T]TCCTTAGAACTACAT | 7874 |
rs150930247 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8918338 | AAAATAGAACTAACT[C/T]ATCTATATTAGATTT | 7874 |
rs150963752 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP7 | GRCh38.p7 | 16:8912109 | AATATCTAACACCCA[A/G]CAAGATAAAAACCAC | 7874 |
rs150996703 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962236 | TCAGGTGGCCTCCAT[C/T]TGACTCCCGACAGCC | 7874 |
rs150999771 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | USP7 | GRCh38.p7 | 16:8941008 | AGGACCCTTCTTCTC[A/G]TCCAGCACTCAGGGA | 7874 |
rs151052898 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8922937 | CAGTTACTGACAGAG[A/T]AAGAATTAAGCCTGG | 7874 |
rs151069472 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8945916 | ATTAAAAAAAACAAC[A/G]GCACTGATTGAGAAA | 7874 |
rs151108474 | in-del | -/A | 0.0123036 | 0.0774623 | intron-variant | USP7 | GRCh38.p7 | 16:8959823 | CACCACCCCCGTAAC[-/A]AAAAAACACAGAAGC | 7874 |
rs151123565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8908932 | TCGGCAGGATTATAA[A/G]CTTCCTTTCCTTGGG | 7874 |
rs151139313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8955964 | AGACAGCCAGATGTC[A/G]GATTACCACCCAGAC | 7874 |
rs151142677 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894168 | CCCCTCAGCGGGGTG[A/G]TGGCCAGTGAGGCAT | 7874 |
rs151175250 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | USP7 | GRCh38.p7 | 16:8930613 | GAATTTGAAAACATG[C/T]TATACCACACTATAA | 7874 |
rs151211038 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8920292 | TCTCTATTACATGCA[C/G]GCTAAAGCTTCTTTC | 7874 |
rs151261257 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8943673 | CATATGGGTAGAGTC[A/G]AATGGCTGGCGGGAA | 7874 |
rs151316347 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8905505 | TGCTAGGCAGGCAGC[A/G]CCTCAGGCATCCGCT | 7874 |
rs151320579 | in-del | -/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8916590 | CAACTCCATTTAAAG[-/C]CTCAACTTTCAAATG | 7874 |
rs151323725 | in-del | -/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8922160 | ACCATCCACAGGCCC[-/T]TGGCTGCATCATAAA | 7874 |
rs151331140 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | USP7 | GRCh38.p7 | 16:8928284 | ATGAGGTGCTTCCCA[A/G]ATTGTGTGCCCTAGT | 7874 |
rs180752719 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950376 | TATTTTAAGAAAAAT[A/T]AAAGCCCTTTAATTT | 7874 |
rs180783110 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8958760 | CCACCAGGCTGACTA[C/T]AGCATCAGTGGCGCA | 7874 |
rs180806889 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8928059 | ACTAAAAGTAGAATG[A/T]GTAGATACAGTAAAA | 7874 |
rs180822423 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8942525 | ACTCTGAATCCCTCT[G/T]GTCTTATTAACAATA | 7874 |
rs180988746 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8954479 | CAATGGGACCACAAT[A/T]CAGCTTGTGAGATTT | 7874 |
rs181005267 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8900924 | AATTCGGGGTAAAAA[C/G]AACAAACAAAACCCT | 7874 |
rs181007337 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938408 | TGTGGATTCAACAAA[C/G]CGCACATCAAAAACA | 7874 |
rs181011580 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8911421 | TTAAGAGTGAAAGGG[C/T]GAGCCACATGCTGAG | 7874 |
rs181015337 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP7 | GRCh38.p7 | 16:8924844 | CTTCATCCCAAATTA[C/T]TTTATTTCACATAAC | 7874 |
rs181087280 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8931548 | TATGTAAAGATCCGG[G/T]AAAGTGTTTAGGAAA | 7874 |
rs181090418 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8955172 | AATGTAATTTTACAT[G/T]TGTTGTATTTAATAA | 7874 |
rs181092779 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | USP7 | GRCh38.p7 | 16:8917833 | CTTGCTCTGTCACCC[A/G]GGCTGGAATGCAGTG | 7874 |
rs181095284 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8946129 | CTCCCCCACAAGACT[C/G]TCAACCTAAACCTCA | 7874 |
rs181099243 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938567 | AATACAAAAACTTAG[A/C]TGGGCACGGTGGCAG | 7874 |
rs181100496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8911973 | AACAACTGAAAGGAT[A/G]TGGGGACAGGTTATC | 7874 |
rs181104885 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893293 | TCTGCCAAGGCAGCA[A/G]AGTAAACCTTAATTG | 7874 |
rs181181444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8925138 | ACAGATGTCAATTCC[C/T]ACATTTTAGGTGAGG | 7874 |
rs181183764 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962726 | GCAGTGCTGTTAGAA[A/C]GTGATTTGGAAGAGC | 7874 |
rs181328124 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | USP7 | GRCh38.p7 | 16:8897789 | CTGTAATCCTAGCTA[C/T]TTGGGGGGCTGAGGT | 7874 |
rs181446672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8915015 | GTGTTAGAAGTCCAC[A/G]TGGTGGTTTCCTGTG | 7874 |
rs181531551 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8946667 | TGGCAAAGGCACACC[G/T]CCAATAATCTGGTCA | 7874 |
rs181537122 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964508 | CAACCCCAGGCGGGG[C/T]GCAGCTGCTCACACC | 7874 |
rs181541376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8932066 | CATGCTCACCTCCCC[C/T]TCCAAGAACTCTCCA | 7874 |
rs181550678 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8903093 | AGGAGTCAGGGGCTC[A/T]ATGGTTTTCTTGCAC | 7874 |
rs181551826 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | USP7 | GRCh38.p7 | 16:8917876 | CTCACTGCAATCTCC[A/G]CCTCCCAGGTCCACG | 7874 |
rs181685274 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP7 | GRCh38.p7 | 16:8953238 | CTCCTATGCCACAGC[C/T]GCTTTGCCGAAGCCC | 7874 |
rs181733107 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8915612 | ACTAGAAATATCAAT[A/G]TTCAAAGAAGTTGTA | 7874 |
rs181733324 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8949200 | AAAATCATGATTGTT[A/T]CCGAATTTTATCAAA | 7874 |
rs181733580 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8927507 | TCATGGAGAACAACA[C/T]TCTAAATCTAGATCC | 7874 |
rs181735167 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8941748 | GGTGCGTGCTGTGAA[C/G]TCAGGCCTGCCTCTC | 7874 |
rs181741199 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8914378 | AACTTGATCCATCAA[A/G]CTGGACATACGCACA | 7874 |
rs181750371 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8934455 | AAGAGCGCATAACAT[C/G]TTACAGGATGGGGTG | 7874 |
rs181750734 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8897939 | TGGATGCGTCTTCTG[C/T]TTGGAGCAAGCAGGT | 7874 |
rs181753770 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8896665 | ATCCTTCCTCTGTTT[C/G]GCTTTTCTATGGGAA | 7874 |
rs181759210 | snp | A/T | 1.65701e-05 | 0.00287833 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8921259 | ATCTCTGTAATTTAT[A/T]ATCTTCAGCACTGCT | 7874 |
rs181777610 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937926 | GAAAATACTGACCAC[A/G]TGAGAAGGAACTACC | 7874 |
rs181877523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8943253 | TCCAAACACTGATGA[C/T]TGGTTTTAATGCTGT | 7874 |
rs181925110 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8935126 | GTGATGTAATACCAA[A/G]TTTTATATGCCACCT | 7874 |
rs181928259 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8906303 | AGCATTTAGCAGCCA[A/G]AGAATACATAGATCA | 7874 |
rs182010819 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8959506 | TCATTAAAACCTGAC[A/G]TGCTCACATCAGAGT | 7874 |
rs182128684 | snp | A/G | 0.00279258 | 0.0372817 | intron-variant | USP7 | GRCh38.p7 | 16:8935619 | CCCTGGATGAAAAAC[A/G]TCTATAGGAAATAAA | 7874 |
rs182147532 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8921984 | TAGGACAGTGCTGTT[C/G]CCACAGCACTTCCTG | 7874 |
rs182153734 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8907542 | TTGTCACTCCTGCAT[C/G]TACTATTTTAACAAC | 7874 |
rs182158067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8928395 | ATTAACAAAAACTTA[C/T]TTTGGATAAGCAATT | 7874 |
rs182173466 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8924194 | CTATTCATTTGCATG[C/T]GGCCATCGGTCAATC | 7874 |
rs182193886 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8905550 | GGACCTTCGCAGTCC[A/C]CATTCAACATTCTGT | 7874 |
rs182197327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8921821 | AGTGAAGTGTGGGGT[A/G]GACCACAAAAGGGCC | 7874 |
rs182280280 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8949886 | ATTACATGAAAATGC[C/T]TGGCTTTCCATATTC | 7874 |
rs182313160 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8955993 | ACACTTGCAGCCCCA[A/C]CCTGGGATGGGACCA | 7874 |
rs182331984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8940299 | CCATGCTTTGTCCAA[C/T]GGCAAATGTCAACAC | 7874 |
rs182333193 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8912751 | TAACACAGCAAGACC[C/T]TGTCTCCAAATAATT | 7874 |
rs182417685 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8933403 | AAACAAAAAAATTCA[C/G]GTACCAAGCGATATG | 7874 |
rs182424674 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8919745 | GCAAAGCAATCCTCC[C/T]ACCTCCACGCCCATC | 7874 |
rs182429756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8895328 | CTCAGCCAGAAGATA[C/T]CCAAGTTTCTTCCCC | 7874 |
rs182434986 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8904056 | CTGTCTGGTGGCCTG[A/G]CTTCTGACAACCAAG | 7874 |
rs182452546 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8910243 | ATCCAAGCGGGGGCT[A/G]GCCACCTGGTCGCCC | 7874 |
rs182480905 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8929887 | GAGGGATTCATAGCT[A/T]TCATCAACTGATATA | 7874 |
rs182494344 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8899013 | AAGCAAGAAATGGAC[G/T]GTCAGGTGAAATGGC | 7874 |
rs182571423 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960923 | CTCATGTGCTCACTA[A/C]AAGAAAAGGGACCTC | 7874 |
rs182615124 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8947307 | AATTATTTTTTATAC[A/C]ACATTACCATGTGCT | 7874 |
rs182723636 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8918963 | GTTTGTTGAGAGGAC[C/T]TTGCTCTGATATACC | 7874 |
rs182752631 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | USP7 | GRCh38.p7 | 16:8916625 | AATTAAAAGTAACTT[A/C]GATTGAAAACCTAAA | 7874 |
rs182804283 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8920143 | TGTCTAGTTGCCATA[A/C]TTATACAATTATGTT | 7874 |
rs182846466 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8943997 | GCGGGGGAGGCAGTA[G/T]ACAGGAGTTCAAGAC | 7874 |
rs182871532 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8947747 | AGTCTTTTAGGACTT[C/T]GACAGGATCCTGCCA | 7874 |
rs182885171 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8934036 | GTGCTGAGATTACAG[A/G]CGTGAAACACCACGC | 7874 |
rs182909601 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950965 | AGTAACCATTCAAGC[G/T]AAGATCTGTGCACAG | 7874 |
rs182912605 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP7 | GRCh38.p7 | 16:8930630 | ATACCACACTATAAT[C/T]TGCTTTATTTGCAAT | 7874 |
rs182922493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8935794 | GTTCCAGGGCCTATA[C/T]TCCCACCTGCTCTAC | 7874 |
rs182975519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894374 | CAGGTTACAAAGGAT[A/G]TAAGGACCTGTTAAG | 7874 |
rs183007699 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8932587 | TAACTAGCTCAAATG[C/T]TCCAAATCAAATATA | 7874 |
rs183021971 | snp | C/T | 0.00686215 | 0.058172 | intron-variant | USP7 | GRCh38.p7 | 16:8903412 | GACTATCTGAAAATA[C/T]GTATGAAAGCACAGA | 7874 |
rs183146192 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8947354 | ACAGCACTCCCCCCC[C/T]CAACACACACACACA | 7874 |
rs183210945 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8898707 | AAATATCTGTGAGTG[A/C]GCATAAAAGCAAACC | 7874 |
rs183268880 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960139 | ACCAAAGTTAGCGAA[C/T]AAATAATACACTGCC | 7874 |
rs183277803 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8929312 | ATTGCCCTCGTCTAC[A/G]GTGGAAAGCGCACTC | 7874 |
rs183281099 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8943420 | AAGTTGCAGCACGCA[A/C]GGCCGGAACCGAGCT | 7874 |
rs183291226 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8916073 | GATTAGTGATGGCGC[A/G]GGGAGAGTAATCACC | 7874 |
rs183347084 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8925882 | TTACTAGGCCAGGTG[C/T]GGTGGCTCACTCCTG | 7874 |
rs183423442 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8955460 | AGGCGCAGTGGCTCA[C/G]ACCTGTAATCCCAGC | 7874 |
rs183447342 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8945125 | GCTGGGTGTGGTGGC[A/G]GGCGCCTGTAATCTC | 7874 |
rs183480595 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8922270 | GAGACAGGCAGATCA[A/C]CTGAGGTCAGGAGTT | 7874 |
rs183569399 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8938950 | GGATTTTGACACCCT[A/G]AGAGGGGTCCTGGAA | 7874 |
rs183594323 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8912270 | CACCCTGGCCAACAT[A/G]GTGAAACCCCGTCTC | 7874 |
rs183622728 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8914570 | AAAGCAACAAAAATG[A/T]TCAAACTATGACTAC | 7874 |
rs183689902 | snp | C/T | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8958340 | CAAGTGCATGTGTGC[C/T]GGGAACCGGCAGCAC | 7874 |
rs183696531 | snp | A/C | 0.0053 | 0.0512046 | utr-variant-5-prime, intron-variant | USP7 | GRCh38.p7 | 16:8936701 | TAGAATCTCTAGGAG[A/C]TCTACCTCAGCATTC | 7874 |
rs183701909 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8927871 | TTCCTTGGGCCAAGT[A/G]CAATGGGTCATGCCT | 7874 |
rs183704671 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, nc-transcript-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8892008 | TTGTCTCCCCAGAAC[C/T]AGTTTAACAAACTCA | 7874 |
rs183708334 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8942511 | GGCCCTCCTAAGTAA[A/C]TCTGAATCCCTCTGG | 7874 |
rs183720000 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP7 | GRCh38.p7 | 16:8908590 | TTAGGTGTCCATTTA[A/G]GGCATCTTTGAAATG | 7874 |
rs183749121 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8952905 | GCACTGGCGCAATCT[C/T]GGCTCACTGCAACCT | 7874 |
rs183767239 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937157 | CCAGGCACTTAGGAC[C/T]CTGAGGCAGGAAGAT | 7874 |
rs183773348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8909495 | CTGAAAGATAAAAGG[A/G]TTCTGTCTCCACCGC | 7874 |
rs183774094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8922730 | CTAAATAGAAGGACC[A/G]TCAAGATTTCTCAGT | 7874 |
rs183820464 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8907792 | GCACTCCAGCCTGGG[C/T]GACACAGCAAGACTC | 7874 |
rs183913393 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8952652 | GATCCTGAATTCAAT[A/G]AGGTCTGCAAAATCC | 7874 |
rs183914747 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8922426 | CCGGGAGGTGGAGGT[A/T]GTGGTGAGCCAAGAT | 7874 |
rs184021107 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | USP7 | GRCh38.p7 | 16:8905029 | ACCATAAGTCTGCAT[C/T]GAAACGCGCAAGCCC | 7874 |
rs184142764 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962295 | TTTAAAGACCATTTG[C/G]ACTTTGCTTTGTTTC | 7874 |
rs184278943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8948664 | TGCGAGAAAAGGGAA[C/T]GACTACTGGCTACGA | 7874 |
rs184286265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8934364 | TTAGAGCTCAAAGAA[A/G]GGCTTGTTTGGGTGA | 7874 |
rs184303216 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | USP7 | GRCh38.p7 | 16:8921010 | TAAGATACGAAACTG[A/G]AGAAAACATGTTTTC | 7874 |
rs184305628 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956757 | AACGAATTAAGACTT[C/T]GTATTAAAAAAACAA | 7874 |
rs184315650 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | USP7 | GRCh38.p7 | 16:8913917 | CCACGCCCAGCTAAT[C/T]TGTAGAGATGGAGTC | 7874 |
rs184319280 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8931110 | TCTACAGCCAATTTT[G/T]TTGTGAAGATTACTG | 7874 |
rs184332637 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8896342 | AGGAATTCACATTCA[A/G]CTGATAGTGGCGTTT | 7874 |
rs184336355 | snp | C/T | 0.000593081 | 0.0172101 | intron-variant | USP7 | GRCh38.p7 | 16:8901130 | CAGAAGGTAAGTGCA[C/T]GAAGGACTTACGTAT | 7874 |
rs184358221 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8948548 | AAGTTCAAATCCCTT[C/T]AAAAATACTGACTAA | 7874 |
rs184361147 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8917210 | GATGCAGGGGAATTT[A/G]AAAAACAGTAAGAAT | 7874 |
rs184366588 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP7 | GRCh38.p7 | 16:8920573 | TTAAATACATCCCAA[C/T]TTTTTTGCTAATTTT | 7874 |
rs184369675 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8900343 | AGAAATTGAGAAGAG[C/T]TTTATGAGATGAAAA | 7874 |
rs184426763 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8945686 | AAGCAGGATTTTTCA[C/T]AGCTAAGGACAAGCT | 7874 |
rs184439990 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP7 | GRCh38.p7 | 16:8917774 | TTTCCTACTTATTGG[A/G]GCACCATTTCTTTTT | 7874 |
rs184498609 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8934121 | TTCCTTGGTTCAAAC[A/T]TACCCTACGACAATA | 7874 |
rs184500498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8904680 | CGGCGTGGTGGCTTA[C/T]GCCTGTAATCCCAGC | 7874 |
rs184573734 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8917442 | GAAGTGCAGTGGCGC[C/G]ACCTCAGCTCACTAC | 7874 |
rs184620892 | snp | C/G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8913406 | AGAAGTGAAGTGAAG[C/G/T]GAAGCGAAGAATATG | 7874 |
rs184626375 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8953070 | TTGAACCCCTGACCT[C/T]GTAATCTGTCGCCTT | 7874 |
rs184731990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8926363 | GCACGCCTGTAATCC[C/T]AGCTACTTGGGAGGT | 7874 |
rs184753126 | snp | A/G/T | 0.000925711 | 0.0214945 | intron-variant | USP7 | GRCh38.p7 | 16:8895763 | AGAGAGGAAAAAAAA[A/G/T]TAGGGCAAAATGAAG | 7874 |
rs184812800 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8945408 | AACAAAAAGTTCCTG[A/G]GAAGACTAGTTGTCC | 7874 |
rs184819499 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961686 | TGTTATTGGATATTT[A/G]TCTTGACCGGGTACC | 7874 |
rs184821596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8930731 | CCTAGCATTTTGAGA[A/G]GCCAAGGCGGACAGA | 7874 |
rs184825303 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8911152 | GGGCAGTGTGGACAA[A/C]CCCTTGGTCTCAAAA | 7874 |
rs184910696 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8954568 | TGGAAGACAATTTAG[C/T]TGTAAGTTTATAGGA | 7874 |
rs184917718 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8941369 | CATATCCTGCAGTCT[A/G]CGGTTAACAACTTTT | 7874 |
rs184929956 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938484 | GTAGGAGGCCGAGGC[A/G]GGTGGATCACAAGGT | 7874 |
rs185034576 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8911511 | GCTCCGGTCATGAAG[A/G]AAAAACGCAACTGCA | 7874 |
rs185038975 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8924866 | TCACATAACCCTGCT[A/G]AGTTGCTTACAGCAC | 7874 |
rs185044833 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893087 | GTGGCAAATTGTACA[C/T]GTTCATTCATTAAAT | 7874 |
rs185120081 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957296 | GTCCAAATTAGTTCA[G/T]AACAAGTAATTTCTA | 7874 |
rs185151369 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8927429 | GCAGTGATTTTAGCA[A/G]ACTTCTGCTCTTCAT | 7874 |
rs185173449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8923136 | AAATCAAAAGGCTAT[A/G]TAGAGGCAGCAAATA | 7874 |
rs185199024 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892414 | ACACACTGGCCCAAA[A/G]ACCAGGAAACCGTGC | 7874 |
rs185249950 | snp | C/G/T | 0.011524 | 0.0751229 | intron-variant | USP7 | GRCh38.p7 | 16:8941703 | TGAGGAGTGAGGGGA[C/G/T]GGGCAGAGCCAGGAT | 7874 |
rs185293726 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937474 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAAC | 7874 |
rs185297305 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | USP7 | GRCh38.p7 | 16:8909775 | TACTAAAAATACAAA[A/G]ATTAGTTGGGCATAG | 7874 |
rs185555833 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8900729 | TTTTCTCTACACCCA[A/G]TTCTATCCACCTTTT | 7874 |
rs185579331 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8907655 | GAGACCAGCCTGGCC[A/C]GCATAGTGAAACCCT | 7874 |
rs185579396 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8922022 | GGGACGCTGACACTG[C/G]GTATGGACCATTCAC | 7874 |
rs185645945 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950596 | ATTTCCCACAGGACT[C/G]GGCGCTGACAGAGAC | 7874 |
rs185660539 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8935656 | ACCATCCCATAATAC[A/G]CATATCCCACTCAGA | 7874 |
rs185665863 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938267 | CTATACTATACTGAC[C/T]TGATTAAACTTTTCT | 7874 |
rs185787736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8932636 | GAGAAAGAAAAGAAA[A/G]ATCAGGTACTCTGAA | 7874 |
rs185791202 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8903471 | TCCACACTGAACACA[C/T]TTAAACACTAAAACG | 7874 |
rs185809396 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | USP7 | GRCh38.p7 | 16:8953515 | ACGTGCCCCATGCGG[C/T]GCCACTGGAAGCAGA | 7874 |
rs185823690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8924323 | TTTATAAAGCATCAT[A/G]AAATTGCCACAGCAA | 7874 |
rs185905640 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8947351 | TCCACAGCACTCCCC[A/C]CCCCAACACACACAC | 7874 |
rs185913867 | snp | A/G | 0.00207489 | 0.0321425 | intron-variant | USP7 | GRCh38.p7 | 16:8918989 | ATACCTGAGAAGAAA[A/G]GGTGAGCGGAAGGCT | 7874 |
rs185937337 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8915628 | TTCAAAGAAGTTGTA[A/G]ACTATAAAAATATGA | 7874 |
rs185939297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8949302 | ACATCGTGGCACGTT[C/T]CACTGGGATTGAAAC | 7874 |
rs185943756 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8928788 | GGGTCCTATGGCGTG[A/G]CACCACTGTCTACTA | 7874 |
rs186027804 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8949954 | CCCCTAGAATAGCAA[A/T]GGAAAACCCCCATTC | 7874 |
rs186029712 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8921907 | GTTTGCGATTTAAGT[G/T]GGGCCTTATCAATCA | 7874 |
rs186046969 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8898224 | AAAGACTGGCCCAGG[A/G]CTCCCCCAGCCCCCA | 7874 |
rs186057268 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8934487 | GGGAAATGCGTAAGC[A/T]CTACCCCCCATTTTT | 7874 |
rs186095740 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8902892 | AAAAAAAAAGAAAAA[A/G]AGACTGTGATTCTAA | 7874 |
rs186151824 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP7 | GRCh38.p7 | 16:8935356 | CTGGGATTACAGGCA[C/T]CTGCCATCATGCCCA | 7874 |
rs186173802 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8931874 | GCTGGCCCCACGGTT[G/T]CCTACACAGTCGGCT | 7874 |
rs186174413 | snp | A/T | 0.000217885 | 0.0104353 | intron-variant | USP7 | GRCh38.p7 | 16:8906379 | GAAGCAGAGCTTGTG[A/T]TAACTTTCTGATGAG | 7874 |
rs186177726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8946253 | ATTTGGACATAATAC[C/T]AAAAGCAAGGTTCAA | 7874 |
rs186178115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8917834 | TTGCTCTGTCACCCA[A/G]GCTGGAATGCAGTGG | 7874 |
rs186391071 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8943551 | ATGAGAAACACAAAC[A/C/G]ACTAACCAACAGGCT | 7874 |
rs186396008 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960255 | GCTTCAGGCCTTACA[A/G]GGAGTGTGTGGTTGC | 7874 |
rs186414269 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8892806 | TTTTATTCAACATAC[A/G]ACATTTTCCAGCAAA | 7874 |
rs186474763 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | USP7 | GRCh38.p7 | 16:8942545 | TATTAACAATATTTG[C/G]CTTACGGCTTATTTA | 7874 |
rs186492660 | snp | C/T | 1.64836e-05 | 0.0028708 | intron-variant | USP7 | GRCh38.p7 | 16:8915348 | CTGGATATAGGACTG[C/T]AAATAAGGAAAGTAA | 7874 |
rs186524557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8932140 | CCTGAATAAAATGGT[A/G]CTCCCCACCACCCAA | 7874 |
rs186550104 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | USP7 | GRCh38.p7 | 16:8959871 | GCTGACCCATTAATT[G/T]GCTCCTAATAGCAGC | 7874 |
rs186589282 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8946991 | TTAAGGTAATGGGGC[A/G]GGGTGAATTAACCTT | 7874 |
rs186597711 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964658 | TTAGCCGGGTGTTGT[G/T]CCTCCTGCCTGTAGT | 7874 |
rs186603933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8926272 | AACCTGAGGTCAGGA[A/G]TTTGAGACCAGCCTG | 7874 |
rs186605866 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8940330 | TGTTATCCAAGAACC[A/G]GAACACCGCCAAATG | 7874 |
rs186612912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8912857 | CTAAAAATAAAAAAA[A/G]ATTTAAAAAGTTTGA | 7874 |
rs186675611 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8959099 | TGCTCCAAATTCCAT[G/T]CCAGGCACTTTAGAT | 7874 |
rs186683285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8956085 | GTTTAACAACTTACT[A/G]TGAGAGCTGGAGGTT | 7874 |
rs186696445 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8928162 | TGTCTCCCATCTCTT[C/T]GTCTCATTAGCTATT | 7874 |
rs186705524 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8897867 | TGGTGCCACTGCACT[C/G]CAGCCTGGGTGACAG | 7874 |
rs186727103 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8905649 | TTCAATCTACTGACA[C/G]TACCAACTCTTTACA | 7874 |
rs186809971 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8943283 | TGTTGTGCACTGAGA[C/G]GGGTTTAATATACAG | 7874 |
rs186812771 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8955361 | GTGATCCTCCCACCT[C/T]GGCCTCCCAAAGTGC | 7874 |
rs186821004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8925192 | TTTACAAAGTGACAA[C/T]AGAGGATTTTAATAT | 7874 |
rs186834980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8929802 | CTCACAGAGAAGCTA[C/T]AGACCAAAACTCAGT | 7874 |
rs186844613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8909338 | ACCTGGAGGAACTGG[A/G]GACCATGACAAGGCA | 7874 |
rs186848744 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891841 | AGGCCCTTGCTGTCA[C/T]GCAGTGGTTTTCAGG | 7874 |
rs186862899 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893848 | ATAGATACAGAGAAG[C/T]CAAACTGAACAGCCT | 7874 |
rs186864422 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8916303 | TTCAAGCTTCCTCAC[A/T]TCACCTTCAAATCCC | 7874 |
rs186923080 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8921522 | ACTCATGGTTTCATT[G/T]TTTAATTCCTTAGAA | 7874 |
rs186939004 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | USP7 | GRCh38.p7 | 16:8947372 | ACACACACACACACA[C/G]GGTCTCACTCTTATC | 7874 |
rs186951439 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | USP7 | GRCh38.p7 | 16:8933782 | TTTTTTTGAGATGGA[G/T]TCTTCCTCTATCTCC | 7874 |
rs187022575 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938644 | ATGAACCTGGGAAGC[A/G]GAGTTGCAGTGAGCG | 7874 |
rs187035552 | snp | A/G | | | utr-variant-5-prime, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8963361 | GGCGGCGGCGAGCCG[A/G]GGCGGCGGCGGCGGC | 7874 |
rs187051188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8912076 | GTCACTTATCTGTGC[A/G]TAAGAGCAAAGGTTA | 7874 |
rs187203270 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8917357 | GGATACTGGAAAACA[C/T]AAGAATGCAAAAATA | 7874 |
rs187209376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8952984 | TGGGATTACAGTCGC[A/G]TGTCACCATGCCAGG | 7874 |
rs187215746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8900437 | AAAACAAAAACGTGG[C/T]TCGGGATCTAGGTAC | 7874 |
rs187272482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961249 | TGTAATCTCAGCAGT[C/T]TGGAAGGACGAGGCG | 7874 |
rs187278685 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8930655 | TGCAATGATATTCTG[C/T]ACAAAACTTTTTATA | 7874 |
rs187285303 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8945175 | GTTGTAGTGAGCCGA[C/G]ATCCTGCCACTGCAC | 7874 |
rs187319886 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937385 | CATCTCTACTAAAAA[C/T]ACAAAAATTAGCCAG | 7874 |
rs187325947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8922856 | CTTTCTGAACAACCC[A/G]TACAAATTAGCTATC | 7874 |
rs187328329 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8917884 | AATCTCCGCCTCCCA[A/G]GTCCACGCCATTCTC | 7874 |
rs187432152 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8919782 | TGTACACAATGCCAC[A/G]ACCTGAACACACGAC | 7874 |
rs187435659 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8904116 | ACCAACAGGGCCAGG[G/T]GTTACAAATACTCAG | 7874 |
rs187663800 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP7 | GRCh38.p7 | 16:8898913 | GGATGTATCTAAAGT[C/T]AGTCTGGCTTTGGAT | 7874 |
rs187702601 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8895332 | GCCAGAAGATATCCA[A/C/G]GTTTCTTCCCCCTCC | 7874 |
rs187903485 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957040 | AATTCTGGAAGCATC[C/G]CTGCTCTGGCTCAGG | 7874 |
rs187909505 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8947762 | CGACAGGATCCTGCC[A/T]TCAAAAACTTAGCTA | 7874 |
rs187915484 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8926382 | TACTTGGGAGGTCGA[C/G]GCAGGAGAATCGCTT | 7874 |
rs187928435 | snp | C/T | 0.000765033 | 0.0195431 | intron-variant | USP7 | GRCh38.p7 | 16:8895785 | AAAATGAAGTATATA[C/T]ATTCACATAAAAATA | 7874 |
rs188002468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | USP7 | GRCh38.p7 | 16:8894485 | GGGCTGCCCCTCCCA[A/G]CCCCAGACCACTTGT | 7874 |
rs188005345 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8942523 | TAACTCTGAATCCCT[C/T]TGGTCTTATTAACAA | 7874 |
rs188009478 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8958624 | ATAGAGACAGCAGAG[C/T]TCAAAGCCGACTCCC | 7874 |
rs188015629 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8927976 | ATAGTGACATCCCAT[C/T]ACTACAAACAATTAG | 7874 |
rs188082831 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8912423 | TGACTGCACTCCAGC[C/T]GGGGCGACAGAGTGA | 7874 |
rs188084950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8925928 | GGGAGGCAGAGGCGG[A/G]TGGATCACGAGGTCA | 7874 |
rs188091170 | snp | A/T | 0.00994011 | 0.0697943 | intron-variant | USP7 | GRCh38.p7 | 16:8904788 | TCTACTACTAAAAAA[A/T]AAAATAAAATAAAAA | 7874 |
rs188142728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8944501 | AGGTCAGAGGTAGAA[A/G]GGAGATTTTTATACA | 7874 |
rs188156374 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8916669 | TATTATTCTCAAATT[C/T]CTTTTCTGTGAAGAT | 7874 |
rs188182214 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8941461 | GAGGGGTAAAGGCAC[A/G]TATCTCCAGCCGCAT | 7874 |
rs188195854 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8935998 | CAATTGGCTGGCTTT[C/T]ATATTTTCTGCCACT | 7874 |
rs188209985 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8913548 | GAACCTGCCAACCTA[C/G]AAGTCTACACCGAGT | 7874 |
rs188214337 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8908198 | TCCTTTAACACTGCG[G/T]CTCTTGGGACACAGA | 7874 |
rs188413106 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960976 | AGGCCCAGTCAGAAG[A/C]AATGAGTTTCTTAAG | 7874 |
rs188450052 | snp | C/T | 0.000181574 | 0.00952648 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8930312 | CTCCATGTCCTCCTC[C/T]GCGGTGTTGTGTCCA | 7874 |
rs188460891 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8899965 | ACTGAGCCAGGCGCA[A/G]TGTAGTGGCTTTACA | 7874 |
rs188471503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8951232 | CAAAGTTGCCTATGA[A/G]GATGTACATCATATA | 7874 |
rs188479448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8922395 | TGAGACGCCGAGGCA[A/G]GAGAATCGCTTGAAC | 7874 |
rs188580856 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8934454 | CAAGAGCGCATAACA[G/T]CTTACAGGATGGGGT | 7874 |
rs188598889 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8905354 | GAAAACAACACACAC[C/G]AGCAGCGATCAAGCA | 7874 |
rs188599081 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8921060 | AGAAAGTAAAAATCT[A/G]ACTCTAAAATCAATA | 7874 |
rs188665414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8949161 | ATTGTGGTATGTGAA[C/T]TATCTCTCAATGAAG | 7874 |
rs188711790 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8952696 | CGTAACATTTGCAGG[C/T]TTCAGCGATTAGGAC | 7874 |
rs188724416 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8922468 | ACTCCAGCCTGGCGA[A/C]AGAGTGAGACTCTGT | 7874 |
rs188845037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8909523 | CGCTGTCCACTGAGG[C/T]TTCGACTCAAATACA | 7874 |
rs188849047 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8892183 | CCCAGCCCAGAACAA[A/C]AACAAGACACCTTAA | 7874 |
rs188924626 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8931932 | AATTAAGAATCTCAA[A/C]TGCATACAGGAGATG | 7874 |
rs188932930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8946637 | TGAACTGACACTCTG[A/G]AGAGCATACAGGCAT | 7874 |
rs188946628 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP7 | GRCh38.p7 | 16:8917850 | GCTGGAATGCAGTGG[C/T]GTGATCTTGGCTCAC | 7874 |
rs188952557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8902920 | TAAGAAAAAGAATTC[C/T]AATTCTTCCCCGGTT | 7874 |
rs188952909 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP7 | GRCh38.p7 | 16:8939989 | TGTAATCCAAGCTAC[C/T]TGGGAGGCTGAGGCA | 7874 |
rs188957037 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8920540 | CCTGTACTTAATAGA[C/G]ATGAAAATACTTTTT | 7874 |
rs188979818 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8936742 | TTTAAAGCATCCCAC[A/G]GAAGCCTTGTCTTTA | 7874 |
rs189058865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8914798 | GTGGCACACGCCTGT[A/G]TTCCCAGCCACTGGG | 7874 |
rs189215600 | snp | A/C | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964185 | GCGGAGGTGAACCGG[A/C]ATCCTTCCCATCCTG | 7874 |
rs189220889 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8955577 | CGGGCATGGCGGCGC[A/G]CCCCTGTAGTCCTGG | 7874 |
rs189229572 | snp | C/T | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8945509 | ATAAACCAACAGACA[C/T]CTTGAACATTTCTGT | 7874 |
rs189231608 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8934101 | GTACACCCAGTACTT[A/T]TAACTTCCTTGGTTC | 7874 |
rs189234635 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP7 | GRCh38.p7 | 16:8911266 | TGGGGTGGAAGTTGG[C/T]CCTGACATCTCCCCA | 7874 |
rs189238647 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8924684 | AGTTCTCAGCATCAG[C/G]CACTTCTCAGGGAAG | 7874 |
rs189239024 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8962068 | ACCAGTCACGCTTAA[C/G]TGTTCCCACCAACCG | 7874 |
rs189242435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8904622 | TTTCCCCTCTTAGAA[A/G]CTCCCGATTCTAGGT | 7874 |
rs189249201 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8892853 | AGAGTTGGTGTACAC[C/T]GCTCCCACAGAAACA | 7874 |
rs189313476 | snp | C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938304 | AACTTTGAGATAACT[C/G]TAGATTCACACACAG | 7874 |
rs189344858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8948566 | AAATACTGACTAAAG[C/T]CTATTACAGATGACA | 7874 |
rs189345135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8920812 | GGTTACCACCTCTGC[A/G]AAAAGCAGCCAAAGT | 7874 |
rs189371975 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8941720 | GGCAGAGCCAGGATC[A/G]GCTGTGTTGGGTGGT | 7874 |
rs189473952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8913922 | CCCAGCTAATTTGTA[A/G]AGATGGAGTCTCACT | 7874 |
rs189479956 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8927490 | ATCCCCACAAATTAG[G/T]TTCATGGAGAACAAC | 7874 |
rs189484142 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | USP7 | GRCh38.p7 | 16:8896464 | TCCAAAAGCCATTTG[C/T]CCTCCAAGCGACTAC | 7874 |
rs189535300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8959110 | CCATGCCAGGCACTT[C/T]AGATGTGCCTGGCGA | 7874 |
rs189578137 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8921967 | ACTCTTCAGGACAAG[A/G]GTAGGACAGTGCTGT | 7874 |
rs189585123 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8906855 | GTTAAGACTACTAAG[G/T]ATATCTGCAAACTGA | 7874 |
rs189605315 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8945733 | TGGAACAATAAAAGA[C/T]TGAGTAGGTAAAACA | 7874 |
rs189612550 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | USP7 | GRCh38.p7 | 16:8917829 | GAGTCTTGCTCTGTC[A/G]CCCAGGCTGGAATGC | 7874 |
rs189858157 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937617 | AGGTGGGACGTAAAG[A/G]CTGCAGTGAGCAAGG | 7874 |
rs189859882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962535 | AGGGCTTTCGCACGG[C/T]TGCAAGCGCACACCT | 7874 |
rs189879561 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8910132 | GAGTCAAGGTTATAA[G/T]ATTACAAAACAGACC | 7874 |
rs189890781 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8931234 | CGCTCTGTCCCCCAG[C/G]CTGGAGTGCAGTGGC | 7874 |
rs189961000 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8943816 | AAAATGAGCATTCAC[A/G]CTGGGGGATAAACAC | 7874 |
rs189968712 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960402 | CCAATGAATATACAA[A/G]GACTGTGCAGAGTTC | 7874 |
rs190006151 | snp | C/T | 1.65274e-05 | 0.00287462 | intron-variant | USP7 | GRCh38.p7 | 16:8902041 | TCCAGGAATCCAACG[C/T]TACTGCTCTAAGTGC | 7874 |
rs190047926 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892434 | GGAAACCGTGCCACG[A/G]AGCTGGAAGGCAAGG | 7874 |
rs190062966 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950810 | GCACTGACCAGCGCA[C/T]GACAGTGATCTGAGC | 7874 |
rs190079365 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8935697 | AGTCTCCATTATTGG[G/T]GATTGCTAGGCCTTT | 7874 |
rs190087625 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8922184 | CATAAAATTACCTTA[A/T]ACATTAAAGAAAATG | 7874 |
rs190089808 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8907656 | AGACCAGCCTGGCCA[G/T]CATAGTGAAACCCTG | 7874 |
rs190107689 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8919288 | ATGGTCACCGATTCC[A/C]TTCTGCTTGCTCCAG | 7874 |
rs190113093 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8953205 | GCTCCCCCTCCCCGC[C/G]GTAAGCCAGTCCTGT | 7874 |
rs190113689 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8954764 | GGTGGATCAGGAGAT[C/T]GAGACCATCCATGGT | 7874 |
rs190119802 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8903633 | GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAC | 7874 |
rs190121167 | snp | C/G | 0.00461891 | 0.0478343 | intron-variant | USP7 | GRCh38.p7 | 16:8923195 | CAAATTTGGCTTCCA[C/G]TAATGAAATACTGTC | 7874 |
rs190123906 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8924965 | CTTCAAGTGGTATTC[A/C]CCTAATCCTTTTGAG | 7874 |
rs190125712 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938528 | CCATCCTGGCTAACA[C/T]GGTGAAACGCCGTCT | 7874 |
rs190130839 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8911749 | GCAGAATGCTGCCCA[C/G]AAAGCGAGATCTGGG | 7874 |
rs190301410 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8930813 | GTCTCTACTAGAAAT[C/G]CAAAAATTAGCTGGG | 7874 |
rs190318434 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8900820 | TTTGATTCTACAACA[C/G]GTAAAAAAAAAAAAT | 7874 |
rs190406985 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8949417 | ACAGTCCCTGAACTT[C/T]ACAACCTCAAAGTCT | 7874 |
rs190415890 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8921726 | AGCTCTGTGGCCTTA[C/G]AGCTTGCTGTCCTGC | 7874 |
rs190569613 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8917619 | CCTGACCTCAGGGGA[C/T]CTGCCCACCTTGGCC | 7874 |
rs190666987 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957857 | CAGTTATTTATGAAA[A/G]TCTATCAATGTCTTT | 7874 |
rs190668887 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8934849 | AGCCACCAAGGTGAT[A/T]CCAGCCCAGCTCCCA | 7874 |
rs190684906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8905824 | CCTAACAGTTATCTT[C/T]CCATCTGCGTTGTGG | 7874 |
rs190877961 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8955772 | ATATAATTTATTCCC[C/T]AAAGTCTTATTGATG | 7874 |
rs190921859 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8935435 | AGGCTGGTCTCGAAC[C/T]CCTGACCTCAGGTGA | 7874 |
rs190924186 | snp | A/T | 1.64784e-05 | 0.00287035 | intron-variant | USP7 | GRCh38.p7 | 16:8916559 | TAAAGTTTCCCACCT[A/T]TCAAAGATAAAACAA | 7874 |
rs190997939 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8940197 | GGCTCCCATCCTGCT[A/G]CCTATCTACGCATCC | 7874 |
rs191002984 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP7 | GRCh38.p7 | 16:8912679 | ATGGTCCCAGCACTT[C/T]GGGAGGCCAAGGCGG | 7874 |
rs191006684 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | USP7 | GRCh38.p7 | 16:8926112 | TGAGCTGAGATCGCG[C/G]CACTGCACTCTAGCC | 7874 |
rs191023217 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8894575 | CTCAAAGTCTTTCAA[A/G]TTTACTTCATACTCG | 7874 |
rs191039262 | snp | A/C/T | 0.00517997 | 0.0506535 | intron-variant | USP7 | GRCh38.p7 | 16:8929043 | TCCCAAGACCTCCCC[A/C/T]CTAAAAAAAAAAAGA | 7874 |
rs191047443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8943304 | TAATATACAGCACAA[A/G]TAAAGAGCTTATAAT | 7874 |
rs191049327 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8915791 | TTTAGAAGCATTTTT[A/G]TATTTTTTACCTCTG | 7874 |
rs191062553 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8898272 | GAGTGTTTTTCTGTG[A/G]TGTCTTAGTTTTCAA | 7874 |
rs191091457 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | USP7 | GRCh38.p7 | 16:8897882 | CCAGCCTGGGTGACA[A/G]AGCGAGACCCTGTCT | 7874 |
rs191123819 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8959995 | CCAGGGAAAAAAACA[A/G]TTTGTATGCAGAAGC | 7874 |
rs191153825 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8929839 | GAATGAAGGCCAAAG[C/T]TTGAATCTGATTTCA | 7874 |
rs191173439 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950108 | ATTTAATTTTATTTA[A/C]ATAGCCACATGTACT | 7874 |
rs191180592 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8928368 | CTCTGAAGTCCAGAG[C/T]CTTAGGGAATCATTA | 7874 |
rs191224323 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893183 | ACTAGTGAGCATGCC[A/C]TCTTGCTAAAAGGCT | 7874 |
rs191330404 | snp | C/G | 1.64838e-05 | 0.00287083 | intron-variant | USP7 | GRCh38.p7 | 16:8915355 | TAGGACTGCAAATAA[C/G]GAAAGTAAAAGTGGT | 7874 |
rs191400989 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8942812 | CTCGGCCTCCAAAAG[C/T]GTTGGGGTTACAGAC | 7874 |
rs191439829 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8912225 | GGGAGGCAGAGGTAC[A/G]TGGATCGCCTGAGGT | 7874 |
rs191442457 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962267 | TGAACTCGTCACGTA[A/G]GTAAGAAAACTTTTT | 7874 |
rs191514541 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8932939 | AATAAATTATGGCAC[A/G]TTCCAATGGAATTTT | 7874 |
rs191528022 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8936936 | CAAACACTGGTGATA[C/T]AAATTGTTAACAACC | 7874 |
rs191548041 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8922577 | GGGCCACTCTGTGGC[A/C/G]TGGCAGGGAGACTAG | 7874 |
rs191555177 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8909480 | TGTTTTTAATACAGT[C/G]TGAAAGATAAAAGGA | 7874 |
rs191561150 | snp | A/C | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891861 | TGGTTTTCAGGGCTC[A/C]CCGCTGTGAAGACTC | 7874 |
rs191627851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8952986 | GGATTACAGTCGCGT[A/G]TCACCATGCCAGGCT | 7874 |
rs191638481 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8923024 | AACAAACTATTTTTA[A/G]TTTTTTCACTTACAA | 7874 |
rs191638666 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937403 | AAAAATTAGCCAGAC[C/G]TGGTGGCGCATGCCT | 7874 |
rs191652279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8899966 | CTGAGCCAGGCGCAA[C/T]GTAGTGGCTTTACAT | 7874 |
rs191688539 | snp | A/C/G | 4.94298e-05 | 0.0049712 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893980 | ACCGTCCTCGCCTTG[A/C/G]ACACACCAGCTTGGA | 7874 |
rs191721608 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8938845 | AGATATTATAAGCCA[A/C]GTAGAGATAATTTAA | 7874 |
rs191831538 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8934225 | AAATCAGGATCACAT[A/G]TAAGTGTAAGCAGTC | 7874 |
rs191840406 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8956295 | TCAATGACCCAAAGA[C/G]AATGATCACCACCTT | 7874 |
rs191843665 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8920937 | TTAGCCCACTGGGAA[A/C]TCCCTTTGAATGTCT | 7874 |
rs191846276 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8904903 | CGAGAACCCGGGAGG[C/T]GGAGCTTGCAGTGAG | 7874 |
rs191849704 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8940515 | GTTACCTTGGGACCA[C/G]GCAACCCAGGGCGGG | 7874 |
rs191955616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8932383 | CCAGCCAGGGAAACA[C/T]AGTGAGACCTCATCT | 7874 |
rs191963748 | snp | A/G | 3.31746e-05 | 0.00407262 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8903397 | AAACTGGTCCTCTGC[A/G]ACTATCTGAAAATAT | 7874 |
rs192016215 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8955362 | TGATCCTCCCACCTC[A/G]GCCTCCCAAAGTGCT | 7874 |
rs192030646 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8951937 | GACTATTCAGGCAGT[C/G]GGCTACTTTCTATAT | 7874 |
rs192031952 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8925545 | ACATTAAATTTTCCA[A/C]GGTACTCCTTAAACA | 7874 |
rs192203016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8947686 | ATTTCTATATGGTAA[A/G]TAACAGTAGCTATAA | 7874 |
rs192218404 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8933913 | GCCGTGTGCCACCAC[A/G]CCCAGCTAATTTTTT | 7874 |
rs192224443 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8896091 | TGATCCGCCCGCCTC[A/G]GCCTCCCGAAGTGCT | 7874 |
rs192230524 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8904221 | GCTCAGGAGAGCACG[A/T]GGAGCAGCTTCTCTC | 7874 |
rs192235090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8919848 | TACTGCGCAGTACCA[C/T]TCACCAGCACCTTGC | 7874 |
rs192258249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8947120 | TCTCTGTAAGATTGG[C/T]TTTTTCATATTTTAA | 7874 |
rs192285710 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8918914 | TGAACTAGCAGCCAT[C/G/T]TGAGGAGACAGGGCC | 7874 |
rs192302570 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957989 | TTTTATGGCTTCAGC[A/G]TCTCTTTCTCAGAGC | 7874 |
rs192377097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8936280 | CTCTGGGTGGCTCAC[A/G]TGGCGCCCTACAGCC | 7874 |
rs192427941 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8917747 | AAATCAGCCCCCAGA[A/G]AACTACTTTTATTTC | 7874 |
rs192504024 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP7 | GRCh38.p7 | 16:8945565 | AGCCATTCATAAGAG[A/G]AAAATCACTGAGACT | 7874 |
rs192551442 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961073 | ATTAACTGTCCTAGG[A/G]GTTACCTTTCTAATA | 7874 |
rs192560817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961424 | TTGAACCCGGGAGAC[A/G]GAGGTTGTAGTGACC | 7874 |
rs192569951 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8909613 | CCAGAATATTTCTTC[A/T]TCACACCAAGTTCTC | 7874 |
rs192571072 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8930704 | CCAGACATGGTGGCT[C/T]ATGCCTGTAATCCTA | 7874 |
rs192573730 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8945265 | GGTGCACACCTGTAA[A/T]CCCAGCTACTCGGGA | 7874 |
rs192592277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8917440 | CTGAAGTGCAGTGGC[A/G]CGACCTCAGCTCACT | 7874 |
rs192595197 | snp | C/T | 0.00235387 | 0.0342257 | intron-variant | USP7 | GRCh38.p7 | 16:8900659 | TATAAAATTGTTACA[C/T]TGCAAGTTTGTCTAA | 7874 |
rs192673218 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8930483 | TTATACTTTTGATGT[C/T]GCCTAATCATTAATA | 7874 |
rs192735234 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8948603 | TAAGAACCTGCACAT[C/G]TCTTTGCTAAATCAT | 7874 |
rs192810096 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8952893 | CCAGGCTAGAGTGCA[C/G/T]TGGCGCAATCTCGGC | 7874 |
rs192814493 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8930962 | CGTCAGGGTGAGACT[C/T]AGTCTCAAATTAAAA | 7874 |
rs192837798 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8944513 | GAAAGGAGATTTTTA[A/C/T]ACATACTCTTGGTTG | 7874 |
rs192889440 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892364 | GAAGGCACACACACT[A/G]CAGTGGAAGTTGAGA | 7874 |
rs192890384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8916827 | CTTTCTCAAGCAAAA[C/T]TCTACAACAAAGTGT | 7874 |
rs192961995 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP7 | GRCh38.p7 | 16:8913218 | AAAATTAGCTGGGCA[C/T]GGTGGCGCATGCCTC | 7874 |
rs192962429 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP7 | GRCh38.p7 | 16:8913766 | ATTTTATTTTACTTT[C/T]TTGAGAGAGATACTT | 7874 |
rs192996419 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8941551 | GCCAAAACACATTTC[A/G]GCTTTTTTGTCCACG | 7874 |
rs193023783 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8934109 | AGTACTTTTAACTTC[C/T]TTGGTTCAAACTTAC | 7874 |
rs193082282 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | USP7 | GRCh38.p7 | 16:8904666 | ATAATCTATTAGGCC[A/G]GCGTGGTGGCTTACG | 7874 |
rs193101483 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891738 | CAGCACGAGCCACCG[C/T]GCCTGGCTGCTCTTC | 7874 |
rs193121728 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP7 | GRCh38.p7 | 16:8922405 | AGGCAGGAGAATCGC[C/T]TGAACCCGGGAGGTG | 7874 |
rs193182518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8927326 | AAAGAAAAAGAAAAA[A/G]AAAAAGAAAGAAAGT | 7874 |
rs193198593 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957042 | TTCTGGAAGCATCCC[C/T]GCTCTGGCTCAGGTT | 7874 |
rs193212545 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8948073 | ATGCCCTGCAGACGT[C/G]AGTCAGCTCCAGCAC | 7874 |
rs193214843 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8920559 | AAAATACTTTTTTTT[A/T]AAATACATCCCAACT | 7874 |
rs193253795 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8908262 | GACTGAAAATATAAA[C/G]ACTGAGGAAAGCACT | 7874 |
rs199516721 | snp | A/C | 0.000389887 | 0.0139568 | intron-variant | USP7 | GRCh38.p7 | 16:8903448 | CTTGACAACTGACAA[A/C]AAATGAGTCCACACT | 7874 |
rs199579856 | in-del | -/AAA | | | intron-variant | USP7 | GRCh38.p7 | 16:8901330 | ACAAACAAAAAAACG[-/AAA]AAAAAAAAACAGTAA | 7874 |
rs199609011 | snp | A/C/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8903300 | TCTGAACAAACTCAG[A/C/G]AAGCGAGGAGTTCTT | 7874 |
rs199651618 | snp | C/G | 0.000675514 | 0.0183658 | intron-variant | USP7 | GRCh38.p7 | 16:8915430 | AATCATCTTTTAGAA[C/G]TGGTAGCCACATACC | 7874 |
rs199666597 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8916589 | AACAACTCCATTTAA[A/C]GCTCAACTTTCAAAT | 7874 |
rs199668929 | in-del | -/GGAAATGTCA | | | intron-variant | USP7 | GRCh38.p7 | 16:8895400 | TATCCCAGTTCCTGT[-/GGAAATGTCA]ACAGCTCTAAATTCA | 7874 |
rs199669046 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8923204 | CTTCCAGTAATGAAA[A/T]ACTGTCTTACGTGGA | 7874 |
rs199682323 | snp | C/T | 0.00338882 | 0.0410235 | intron-variant | USP7 | GRCh38.p7 | 16:8905351 | AAGGAAAACAACACA[C/T]ACCAGCAGCGATCAA | 7874 |
rs199710388 | snp | C/T | 0.00199792 | 0.0315431 | intron-variant | USP7 | GRCh38.p7 | 16:8906409 | GCTTGCATTCAGCCC[C/T]GGGTCCCACCACTTA | 7874 |
rs199828332 | snp | A/G | 0.00014846 | 0.0086144 | intron-variant | USP7 | GRCh38.p7 | 16:8895624 | CTCTCTGGTGCCAAC[A/G]GTATCGGGGACAGAT | 7874 |
rs199832315 | snp | A/G | 0.00199792 | 0.0315431 | intron-variant | USP7 | GRCh38.p7 | 16:8905161 | CCACCACAGTAAAGA[A/G]CAGAACAAAAGTGAA | 7874 |
rs199887318 | snp | A/C/G | 8.29365e-05 | 0.00643911 | intron-variant | USP7 | GRCh38.p7 | 16:8894644 | TGCAAATTTAAACTA[A/C/G]AAGAAAAAAAATTAA | 7874 |
rs199897259 | snp | C/G/T | 6.64557e-05 | 0.00576405 | intron-variant | USP7 | GRCh38.p7 | 16:8904608 | CCCTGCAGATGGACT[C/G/T]TCCCCTCTTAGAAGC | 7874 |
rs199904984 | in-del | -/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8897697 | GAGACCCTGTCTCTA[-/C]CAAAAAAAAAAAAAA | 7874 |
rs199930651 | in-del | -/A | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957592 | CAAAACTTAAAATTC[-/A]AAAAAAAAAAAAAAA | 7874 |
rs199972168 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8929045 | CCAAGACCTCCCCCC[A/T]AAAAAAAAAAAGAAA | 7874 |
rs200010980 | snp | A/G | 9.93114e-05 | 0.00704598 | intron-variant | USP7 | GRCh38.p7 | 16:8901239 | CATTACATCATCTAC[A/G]AGGTTAATAAACAAG | 7874 |
rs200020200 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8923208 | CAGTAATGAAATACT[A/G]TCTTACGTGGAATCA | 7874 |
rs200033645 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8916419 | TTTTCTGAATTAGGT[G/T]TGAGGTTTTACTTGG | 7874 |
rs200042321 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8902792 | ACTTGGGAGGCTGAG[A/G]CAGGAGAATTGCTTG | 7874 |
rs200093887 | in-del | -/GAAGT | 0.00716266 | 0.059414 | intron-variant | USP7 | GRCh38.p7 | 16:8913391 | AGACAGGAGAGAAGA[-/GAAGT]GAAGTGAAGTGAAGC | 7874 |
rs200102977 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961504 | TCTCAAAAAAAAAAA[A/G]GGGGGGGGGGGGCAA | 7874 |
rs200123362 | in-del | -/A | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956762 | TTAAGACTTCGTATT[-/A]AAAAAAACAAAAACA | 7874 |
rs200156369 | snp | C/T | 0.00199792 | 0.0315431 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8919111 | GATTCTTTAAGCCGA[C/T]GTAGCCTGTGTGCTT | 7874 |
rs200180798 | snp | A/T | 0.000329734 | 0.0128358 | intron-variant | USP7 | GRCh38.p7 | 16:8896991 | AATTGGGCTCAAGAA[A/T]TACTTGCCTAAGTTT | 7874 |
rs200187793 | snp | A/G | 1.64768e-05 | 0.00287021 | intron-variant | USP7 | GRCh38.p7 | 16:8905341 | ACACCACTGCAAGGA[A/G]AACAACACACACCAG | 7874 |
rs200203429 | in-del | -/GAAGT | | | intron-variant | USP7 | GRCh38.p7 | 16:8913392 | AGACAGGAGAGAAGA[-/GAAGT]GAAGTGAAGCGAAGC | 7874 |
rs200210556 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8903420 | GAAAATATGTATGAA[A/G]GCACAGAAAAGACTT | 7874 |
rs200262999 | snp | C/T | 1.66952e-05 | 0.00288917 | intron-variant | USP7 | GRCh38.p7 | 16:8899234 | GGGGAAAAATTGAAA[C/T]TTGGTCATAAACTTC | 7874 |
rs200265162 | snp | C/T | | | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8919062 | GTGAAAAATAACGTC[C/T]GTAGCAGGCTGTTCA | 7874 |
rs200295055 | in-del | -/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8944245 | TGCAAAAAAAAAAAA[-/G]CACAGCCAAAATACT | 7874 |
rs200358849 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8947357 | GCACTCCCCCCCCCA[A/C]CACACACACACACAG | 7874 |
rs200389222 | snp | C/G | 0.00199792 | 0.0315431 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8923279 | GGTGTGGTCTGTCTG[C/G]ATAAAAGCGTGGCAT | 7874 |
rs200500408 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8920969 | ACTAAAAAGTGAGAC[A/G]TGAATCCAGAAAGCT | 7874 |
rs200639055 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8930973 | GACTCAGTCTCAAAT[A/T]AAAAAAAAAAAAAAA | 7874 |
rs200680132 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957762 | ACCCTGTCTCTTAAA[A/T]TAAAAAAAAAACAAA | 7874 |
rs200697140 | snp | A/G | 1.68173e-05 | 0.00289972 | intron-variant | USP7 | GRCh38.p7 | 16:8915220 | CAGTAGAAATCATCA[A/G]AAGATCATGCCATTA | 7874 |
rs200702953 | snp | A/G | 4.94173e-05 | 0.00497053 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8895070 | GATTCCGAACGTTCC[A/G]AAGACCTCTTTGTGG | 7874 |
rs200774924 | snp | A/C | 0.00299557 | 0.0385851 | intron-variant | USP7 | GRCh38.p7 | 16:8920318 | CTTTCACTGCAGCAC[A/C]AAAGACATTTTTAAC | 7874 |
rs200786560 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8901321 | ACAAACAAAAAAACG[A/G]AAAAAAAAAAACAGT | 7874 |
rs200818013 | snp | A/G | | | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8902135 | GCCAGCTCGGGATCA[A/G]CTGTTTCCAGGAATA | 7874 |
rs200840623 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8952083 | AAAAGTAGACCCCCC[C/G]GTCTATACAAAAAAG | 7874 |
rs200850233 | snp | C/T | 2.02583e-05 | 0.00318257 | intron-variant | USP7 | GRCh38.p7 | 16:8895764 | GAGAGGAAAAAAAAA[C/T]AGGGCAAAATGAAGT | 7874 |
rs200907259 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8932623 | TAAATTTAAAAAAGA[A/G]AAAGAAAAGAAAAAT | 7874 |
rs200922095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8899209 | ACACAGAAAGGAAGG[C/T]TCACATTTTGGGGAA | 7874 |
rs200955473 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8949980 | CATTCACAGGCTCTG[C/T]CTAAACAGCAGTGCT | 7874 |
rs200960692 | in-del | -/GCCTCTTAAG | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8951270 | AATCTTTAAAATCTG[-/GCCTCTTAAG]TCACCTAATTTCCTT | 7874 |
rs200992662 | snp | C/G | 0.000149265 | 0.00863772 | intron-variant | USP7 | GRCh38.p7 | 16:8904597 | TCCTCTTTGACCCCT[C/G]CAGATGGACTTTCCC | 7874 |
rs201033241 | snp | C/G | 0.467266 | 0.123675 | intron-variant, missense | USP7 | GRCh38.p7 | 16:8894529 | ACCCACACCAGCCCC[C/G]GGGGGGGGGAGAACC | 7874 |
rs201039182 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8912775 | AATAATTATAATTAA[C/T]TGATAAATACATAGA | 7874 |
rs201085716 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8944232 | AGAGCAACAGAGGTG[A/C]AAAAAAAAAAAAGCA | 7874 |
rs201116842 | snp | A/G | 0.000247078 | 0.0111121 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8905314 | CCTTGACACCACGTC[A/G]TCATCAAATTTACAC | 7874 |
rs201136939 | in-del | -/TCT | | | intron-variant | USP7 | GRCh38.p7 | 16:8916356 | CTTTATAACTAGACA[-/TCT]GCTGCCTTTTTGTAG | 7874 |
rs201141976 | snp | G/T | 6.59033e-05 | 0.00573997 | intron-variant | USP7 | GRCh38.p7 | 16:8894736 | GCTACGCTAGGCAAG[G/T]CTTGAGCCTATGGCC | 7874 |
rs201149864 | snp | C/T | 8.2991e-05 | 0.00644117 | intron-variant | USP7 | GRCh38.p7 | 16:8903258 | GTATATCCACGGGAC[C/T]GGTACGCACCATGGT | 7874 |
rs201187611 | snp | C/T | | | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8917091 | TAATTCATAGAACAC[C/T]CTTTGTAATGCTAAA | 7874 |
rs201226219 | snp | A/C/T | 0.000195317 | 0.00988043 | intron-variant | USP7 | GRCh38.p7 | 16:8930447 | CATTCATGGCTTTAA[A/C/T]AGAATAAGCAAAATA | 7874 |
rs201268930 | snp | A/G/T | 9.92185e-05 | 0.00704276 | missense, synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8894590 | ATTTACTTCATACTC[A/G/T]TCTTCATTTATGTAC | 7874 |
rs201290001 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937223 | TTTTTTAAAAAAAAA[A/G]GGATTAACACGAAAC | 7874 |
rs201347539 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957764 | CCTGTCTCTTAAATT[A/T]AAAAAAAAACAAAAA | 7874 |
rs201366887 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8923209 | AGTAATGAAATACTG[C/T]CTTACGTGGAATCAG | 7874 |
rs201386037 | snp | A/C/G | 0.000103401 | 0.0071897 | intron-variant | USP7 | GRCh38.p7 | 16:8900944 | AACAAAACCCTCCAC[A/C/G]AACTACTAAGAATAT | 7874 |
rs201390988 | snp | A/G | 0.00199806 | 0.0315443 | intron-variant | USP7 | GRCh38.p7 | 16:8905142 | ATGGTACAAATGTCC[A/G]AGTCCACCACAGTAA | 7874 |
rs201458798 | snp | A/G | 3.33996e-05 | 0.0040864 | intron-variant | USP7 | GRCh38.p7 | 16:8904409 | GCTGCATGGTGACCC[A/G]GAGTCCCAGAAGGGC | 7874 |
rs201479577 | in-del | -/C | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957774 | AAATTAAAAAAAAAA[-/C]AAAAAAAAATTAAAA | 7874 |
rs201497079 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8930349 | AGGGCCACATTCCCA[C/T]TGATCACAGGGTTCT | 7874 |
rs201557390 | in-del | -/AAAG | 0.00196507 | 0.0312838 | intron-variant | USP7 | GRCh38.p7 | 16:8898447 | CTTAAGCTATTAAGA[-/AAAG]AAAGATTCACATCAG | 7874 |
rs201559989 | snp | A/G | 0.000199081 | 0.00997501 | intron-variant | USP7 | GRCh38.p7 | 16:8917164 | TACACAGCCTGAAAC[A/G]ATTAAGAAATAAGAA | 7874 |
rs201563482 | snp | A/G | 2.45095e-05 | 0.00350059 | intron-variant | USP7 | GRCh38.p7 | 16:8906626 | AGTATTAATTTACAC[A/G]AAAAATATCACACTT | 7874 |
rs201611793 | in-del | -/ATC | 0.0111196 | 0.0737302 | intron-variant | USP7 | GRCh38.p7 | 16:8929887 | GAGGGATTCATAGCT[-/ATC]ATCAACTGATATACA | 7874 |
rs201638486 | in-del | -/TTATTTTG | 0.00734085 | 0.0601376 | intron-variant | USP7 | GRCh38.p7 | 16:8919607 | CTCCCAGAGCTTTTT[-/TTATTTTG]TTATTTTGTGATTTT | 7874 |
rs201664180 | snp | A/G | 0.00107065 | 0.0231124 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893968 | GGCCACCCACACACC[A/G]TCCTCGCCTTGAACA | 7874 |
rs201697945 | snp | A/G | 1.86607e-05 | 0.00305451 | intron-variant | USP7 | GRCh38.p7 | 16:8898682 | ATGACTTGTTTATTT[A/G]CCTAAAAACAAATAT | 7874 |
rs201711302 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8923207 | CCAGTAATGAAATAC[A/T]GTCTTACGTGGAATC | 7874 |
rs201722780 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8895737 | AGCTTACAATTTCTA[A/G]CAGCCTGAACAGAGA | 7874 |
rs201756606 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8951270 | AATCTTTAAAATCTG[G/T]CCTCTTAAGTCACCT | 7874 |
rs201796761 | in-del | -/C | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956779 | AAAAACAAAAACAAA[-/C]AAAAAAAAAACACTG | 7874 |
rs201798776 | snp | A/G/T | 0.00379496 | 0.043395 | intron-variant | USP7 | GRCh38.p7 | 16:8894680 | CTCCGTTATTTCTGT[A/G/T]TATCAGCAAAACTCA | 7874 |
rs201850689 | in-del | -/T | 0.00874735 | 0.0655527 | intron-variant | USP7 | GRCh38.p7 | 16:8930634 | CACACTATAATTTGC[-/T]TTATTTGCAATGATA | 7874 |
rs201852256 | snp | C/T | | | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8915482 | TTGGGTATGGTGCCC[C/T]CTACACAGGTGCCTT | 7874 |
rs201855673 | snp | C/T | 0.000131833 | 0.00811782 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8903323 | GAGTTCTTCAATACT[C/T]TGAACACAGTGTATT | 7874 |
rs201870500 | snp | C/G/T | 0.0011197 | 0.0236349 | intron-variant | USP7 | GRCh38.p7 | 16:8894999 | GGCTCCAGGTTTTGA[C/G/T]GTGAGCCACTCGGCC | 7874 |
rs201871189 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8903214 | TCTAGTGACACGGAA[A/G]GAAGGTGGACGTTGG | 7874 |
rs201904430 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8933391 | CAACTCTATTAAAAA[C/T]AAAAAAATTCAGGTA | 7874 |
rs201923272 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | USP7 | GRCh38.p7 | 16:8929197 | CGCCTCAGAGCTGGC[C/G]ATGCCTTCCCAAATG | 7874 |
rs201963376 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8923210 | GTAATGAAATACTGT[C/G]TTACGTGGAATCAGA | 7874 |
rs201963438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8949671 | ATTTCCAGGCCCCTA[C/T]CTGCTCACCTCTGTG | 7874 |
rs201987652 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8905164 | CCACAGTAAAGAACA[A/G]AACAAAAGTGAACAC | 7874 |
rs202009120 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8930584 | AAACTTTCGCTGTTT[C/T]GAAACACTAAATGGA | 7874 |
rs202021946 | snp | A/G | 4.9423e-05 | 0.00497082 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8897034 | CTCCCCAAGCTCCAC[A/G]GCCTTTTTACATTCT | 7874 |
rs202027586 | in-del | -/TTTG | 0.0150606 | 0.0854603 | intron-variant | USP7 | GRCh38.p7 | 16:8908633 | CTGTTTATGGGTCTC[-/TTTG]TTTATTAAAATAATG | 7874 |
rs202081136 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8912449 | AGTGAGACTCCATGT[A/C]AAAAAAAAAAAAAGA | 7874 |
rs202093533 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8925489 | TTTATGTATACAAAA[-/A]TCAATACATATTGTA | 7874 |
rs202136325 | snp | C/G/T | 0.00311515 | 0.039344 | intron-variant | USP7 | GRCh38.p7 | 16:8916987 | AAAAAAAAAAAAAAA[C/G/T]AGGAAGCAGAATGGC | 7874 |
rs202149594 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8929019 | GCTCCGCCCTATATC[G/T]ATGTCTCCTCCCAAG | 7874 |
rs202171283 | in-del | -/AGGTGGCTC | 0.0463947 | 0.145069 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957471 | TAAACGGGCTGGGTG[-/AGGTGGCTC]ACACCTATAATCCCA | 7874 |
rs202185441 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8905154 | TCCAAGTCCACCACA[A/G]TAAAGAACAGAACAA | 7874 |
rs202210588 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8934751 | CAAGGCCAGTGGCTG[G/T]GAAATGGCAAAGGGC | 7874 |
rs202226527 | snp | A/T | 0.00199809 | 0.0315444 | intron-variant | USP7 | GRCh38.p7 | 16:8923433 | AAAAAAAACACATCA[A/T]CAGTCACAGAGCCTG | 7874 |
rs202239204 | in-del | -/A | 0.00491891 | 0.0493483 | intron-variant | USP7 | GRCh38.p7 | 16:8915386 | TAACTAGTAATAGTC[-/A]AAAAAATTCACATTC | 7874 |
rs207475758 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8899537 | AGCTTCTTCAACAAG[A/C]ATTTTAAGAAAGAAA | 7874 |
rs367558286 | snp | A/G | 8.2373e-05 | 0.00641714 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8919112 | ATTCTTTAAGCCGAC[A/G]TAGCCTGTGTGCTTC | 7874 |
rs367567960 | snp | A/G | 0.000132957 | 0.00815234 | intron-variant | USP7 | GRCh38.p7 | 16:8930273 | CGCCCACTGCGAGGC[A/G]GTGAACCACAGGCAC | 7874 |
rs367661939 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8935078 | GACAGATGTACAACA[C/T]TGGCATGCACATACA | 7874 |
rs367672731 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8953392 | GCCTACACCAGCCTC[C/T]GTGGACACTACAGGA | 7874 |
rs367703877 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8956112 | GGTTAGTACATAACA[A/C]AGGACACTGTCCTCC | 7874 |
rs367720100 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8897718 | AAAAAAAAAAAAAAA[A/T]AAAAAAAAATATATA | 7874 |
rs367783870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8951884 | CTTCATCTCTTTTTA[C/T]GCCACCAAATGCCAC | 7874 |
rs367797644 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8954523 | TTAACCGTAACTCAA[A/G]AAGTCAAATCCACAA | 7874 |
rs367885959 | snp | A/C/G | 3.29529e-05 | 0.00405901 | intron-variant | USP7 | GRCh38.p7 | 16:8894735 | CGCTACGCTAGGCAA[A/C/G]GCTTGAGCCTATGGC | 7874 |
rs367918467 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8912140 | CATGCCTGCTGTTCA[A/G]TAAAAAAGTTACCAA | 7874 |
rs367926743 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8934431 | AATAATAAAAACCAA[A/G]ATCAATTCAAGAGCG | 7874 |
rs367978469 | snp | A/C | 1.65034e-05 | 0.00287253 | intron-variant | USP7 | GRCh38.p7 | 16:8899599 | AAGGAGCATTTATTA[A/C]ATACCTGAAAATAAT | 7874 |
rs368035727 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957190 | GACTTCTCATTAGCT[C/G]AGGCATGTGTTAACT | 7874 |
rs368038937 | snp | A/T | 3.3614e-05 | 0.0040995 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8902459 | TTGCATGGGCCACAA[A/T]CGAATTTGATCTTGT | 7874 |
rs368065686 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8927030 | GTTGCAAAAAGAAAG[C/G]TAGGCCGGGCGCAGT | 7874 |
rs368076615 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | USP7 | GRCh38.p7 | 16:8910690 | TAGCAATTAAAAGAA[C/T]TGAAAATAAAGAAGA | 7874 |
rs368085455 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8940673 | TAAGAAGCTCCTGAC[C/T]GCCATCTTCTAGACA | 7874 |
rs368126122 | snp | C/T | 3.29723e-05 | 0.00406018 | intron-variant | USP7 | GRCh38.p7 | 16:8918996 | AGAAGAAAGGGTGAG[C/T]GGAAGGCTGCAGGAG | 7874 |
rs368175574 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8955703 | GAGCACGATTCCATC[A/T]CAAAAAAAAAAAAAA | 7874 |
rs368196563 | snp | C/G | 1.6495e-05 | 0.0028718 | intron-variant | USP7 | GRCh38.p7 | 16:8915384 | GTTTAACTAGTAATA[C/G]TCAAAAAATTCACAT | 7874 |
rs368229841 | in-del | -/GTC | | | utr-variant-3-prime, nc-transcript-variant, cds-indel | USP7 | GRCh38.p7 | 16:8893207 | AAAGGCTTTCTTGTC[-/GTC]TGTTCCACTTTAACG | 7874 |
rs368295047 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8899360 | CACCATGGGAGTAGC[A/G]TATCTGATGAAGATA | 7874 |
rs368304583 | in-del | -/GACATGGTAAA | | | intron-variant | USP7 | GRCh38.p7 | 16:8934939 | TAAAATTTTAATTAA[-/GACATGGTAAA]TCCCTAGTCCAGAAG | 7874 |
rs368313006 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | USP7 | GRCh38.p7 | 16:8955047 | AGATGAATGACAGTG[C/G]TGTGTGGACCAGTCA | 7874 |
rs368316120 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8943794 | CCACAAAAACCCATT[C/T]CCCAAGAAAATGAGC | 7874 |
rs368329036 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892492 | CACGATAGCGCCTGC[C/T]GCCCCGAAGGGCCTC | 7874 |
rs368339567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961284 | GATCACCTGAGGTCG[A/G]GAGTTCGAGACCAGC | 7874 |
rs368358749 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937094 | AAGCAGGAGGAATAA[C/T]TGATGTAAGTGAAAA | 7874 |
rs368373081 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8897834 | AGCCCAGGAGGTCTA[C/T]GCTGTCGTGGGCTGT | 7874 |
rs368420760 | snp | A/T | 3.30087e-05 | 0.00406242 | intron-variant | USP7 | GRCh38.p7 | 16:8899101 | TCAAGACCAAGCAAG[A/T]GTCCACACATGTGAC | 7874 |
rs368436263 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8940420 | CTTCTTGAACACAAC[A/G]AGAGGCAGAAGGTGT | 7874 |
rs368441224 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | USP7 | GRCh38.p7 | 16:8904396 | AGATGGGTGCCCGGC[C/T]GCATGGTGACCCGGA | 7874 |
rs368446013 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8926351 | GGGTGTGGTGGTGCA[C/T]GCCTGTAATCCCAGC | 7874 |
rs368465591 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8943577 | AGGCTCCACCTCCCT[C/T]GTTAACGTGGGATAC | 7874 |
rs368469681 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8920861 | AGTCACATGGAACCA[C/T]TCAGTACTATGCCTG | 7874 |
rs368475376 | in-del | -/TG | | | intron-variant | USP7 | GRCh38.p7 | 16:8908670 | CACCAGCACTGACTG[-/TG]AGAGATTCTCTTACC | 7874 |
rs368574068 | snp | A/G | 4.98442e-05 | 0.00499196 | intron-variant | USP7 | GRCh38.p7 | 16:8894669 | AATTAAAACTCCTCC[A/G]TTATTTCTGTATATC | 7874 |
rs368588641 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950791 | ACATGCATGTCTTCC[C/G]CAGGCACTGACCAGC | 7874 |
rs368596833 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956633 | GCCGGGCATGGTAGC[A/G]TGTGCCTGTAGTCCA | 7874 |
rs368597858 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892332 | ATCACACGGGTCACA[A/G]GGCAGCTCTCAGAGC | 7874 |
rs368613298 | snp | A/G | 0.000231191 | 0.010749 | intron-variant | USP7 | GRCh38.p7 | 16:8896963 | TAACTGCCACCCCTA[A/G]CTGAACGTCCACAAT | 7874 |
rs368631123 | in-del | -/A | 0.00755907 | 0.0610114 | intron-variant | USP7 | GRCh38.p7 | 16:8943358 | TATAGTCTGCTCCGC[-/A]AAAGAAACAGGATTA | 7874 |
rs368671418 | in-del | -/AGGCCCACCTGGGGCATGC | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8952598 | GACTGTGAGTACACT[-/AGGCCCACCTGGGGCATGC]AGGCCCACCTCCTCA | 7874 |
rs368745630 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8896928 | GTGATTTCCACCAAC[A/G]CAACTGCAGAGGTCA | 7874 |
rs368781240 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8946051 | TGACAAAGGTACAAA[A/G]GCAATTCAACGGACA | 7874 |
rs368786431 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8896712 | CAGCTAATGTTATCA[A/G]AAGATACAAGGGGAA | 7874 |
rs368803400 | snp | A/C/T | 8.24404e-05 | 0.00641986 | intron-variant | USP7 | GRCh38.p7 | 16:8910722 | CGCTACAACAGGACA[A/C/T]TAGCACAAAACACTC | 7874 |
rs368811127 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892607 | GACTAGTTAGAGGCT[A/G]AAAAAAAAAAAAAAA | 7874 |
rs368837913 | snp | C/T | 0.000115303 | 0.00759199 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894076 | GAAGTGGTCGAGCCC[C/T]AGCCAAGGCCGAGGA | 7874 |
rs368846636 | snp | G/T | 1.65466e-05 | 0.00287628 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8899167 | GATCTGTGTTGAGCC[G/T]CTGTGCAACTGTCTT | 7874 |
rs368851917 | snp | A/G | 0.000307953 | 0.0124049 | intron-variant | USP7 | GRCh38.p7 | 16:8902046 | GAATCCAACGCTACT[A/G]CTCTAAGTGCAGGCA | 7874 |
rs368894909 | snp | C/T | 4.9423e-05 | 0.00497082 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8897033 | TCTCCCCAAGCTCCA[C/T]GGCCTTTTTACATTC | 7874 |
rs368915498 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8927617 | AAGGCAGGTGGATCA[A/C]CTGAGGTCAGGTGTT | 7874 |
rs368934250 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8933719 | TCTCCCAAAATGCTG[A/G]GATTACAGGCATGTG | 7874 |
rs368946107 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893629 | CTAGCTGCAGGGCTG[A/G]TGCACGGGACCCCAG | 7874 |
rs368964730 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8910085 | AGCACAGGCCAGACT[C/G]ACATTTTTAATTATA | 7874 |
rs368975487 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956884 | GAGGACTCCCAGCGC[A/T]GCCTCAGCCATGCCC | 7874 |
rs369014271 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8928221 | CTAAGAAGTCTTCTG[C/T]GCAAATCAGTCAAGT | 7874 |
rs369161750 | snp | A/G | | | intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8963060 | ACTTTGCAGCCTCGC[A/G]GGCCGGGGCCGGGAG | 7874 |
rs369225461 | snp | C/T | 0.000214743 | 0.0103598 | intron-variant | USP7 | GRCh38.p7 | 16:8898484 | CCGTCACCAAAACCC[C/T]GAGCCTTCTCTTTAT | 7874 |
rs369253853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8928539 | CCCTGAAGAAGAGGA[C/T]TGCGCAATTTGTACT | 7874 |
rs369258514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8910658 | AACACATGAAAAGGC[A/G]CAAGCAAATTTTTAT | 7874 |
rs369303467 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8955486 | CCAGCACTTTGGGAG[A/G]CCGAGTGAGGCAGCT | 7874 |
rs369321319 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | USP7 | GRCh38.p7 | 16:8930431 | AATTCCACGGGTTTT[A/C]CATTCATGGCTTTAA | 7874 |
rs369349080 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8953255 | CTTTGCCGAAGCCCT[C/T]CCCTGCACACGTGTT | 7874 |
rs369363342 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8896895 | AGTCTGGGAATGACG[C/T]GCATGGATCCCAGCT | 7874 |
rs369365620 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8923454 | ACAGAGCCTGTGCAT[A/T]GACCAAAAGCACTAG | 7874 |
rs369394073 | in-del | -/TT | 0.00358779 | 0.0422022 | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891751 | CGCGCCTGGCTGCTC[-/TT]CTCATTTTGAAACAA | 7874 |
rs369427631 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8945236 | TCTTCAAAAAAAAAA[C/T]AGCCAGGTGTGGTGG | 7874 |
rs369433236 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8955879 | ACACATTCAGAGGAA[G/T]GCCACATGGTGTCCC | 7874 |
rs369435839 | snp | C/T | 1.64806e-05 | 0.00287054 | intron-variant | USP7 | GRCh38.p7 | 16:8894899 | CAGTCACTCCCAGCA[C/T]CCCCAGGCCACGTCA | 7874 |
rs369447614 | snp | C/G | 0.000132639 | 0.0081426 | intron-variant | USP7 | GRCh38.p7 | 16:8915534 | CGAGCAACTGAAAAA[C/G]AATGTTTTGGCTTTA | 7874 |
rs369469439 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8963033 | CCGCCCCTCGCCCGC[A/G]GACCCGGCATGACTT | 7874 |
rs369470236 | snp | A/G | 6.58935e-05 | 0.00573955 | intron-variant | USP7 | GRCh38.p7 | 16:8895011 | TGACGTGAGCCACTC[A/G]GCCAACCACAACAGC | 7874 |
rs369475303 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938298 | TGATTAAACTTTGAG[A/G]TAACTGTAGATTCAC | 7874 |
rs369499576 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8941861 | GGAACTGGGTGGACA[C/T]GCCTCCTGGTCTCCT | 7874 |
rs369524653 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8918828 | AAGAAAAAGGTTGGC[A/G]GTGGTAACTCTGAAT | 7874 |
rs369533422 | in-del | -/A | 0.0115144 | 0.0749975 | intron-variant | USP7 | GRCh38.p7 | 16:8900411 | CTCAACAGTTACATT[-/A]AAAAAAAACAAAAAC | 7874 |
rs369544552 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8952968 | CGGCCTCCCAAGTAG[A/C]TGGGATTACAGTCGC | 7874 |
rs369561318 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8923155 | AGGCAGCAAATAACT[A/T]AAGATAAAATTGCAC | 7874 |
rs369565721 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937180 | AGGAAGATCCCTTTA[C/G]CCTGGGCAACACAGT | 7874 |
rs369568767 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | USP7 | GRCh38.p7 | 16:8903255 | GGGGTATATCCACGG[A/G]ACCGGTACGCACCAT | 7874 |
rs369569243 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8908265 | TGAAAATATAAAGAC[G/T]GAGGAAAGCACTGAG | 7874 |
rs369579319 | snp | C/T | 3.29957e-05 | 0.00406162 | intron-variant | USP7 | GRCh38.p7 | 16:8902064 | CTAAGTGCAGGCAGG[C/T]GTCTCGTGGGCACTT | 7874 |
rs369630717 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8927949 | AAGAAGTTCAAGACC[A/T]GCCTGGGTAACATAG | 7874 |
rs369652463 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8952027 | CGACTTTTGGGTGGT[A/G]AGGTAGGAAAATGGA | 7874 |
rs369678554 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8919268 | TTATCACACAGCATC[C/G]TTCAATGGTCACCGA | 7874 |
rs369690182 | snp | C/T | 0.00126984 | 0.0251656 | intron-variant | USP7 | GRCh38.p7 | 16:8916581 | ATAAAACAAACAACT[C/T]CATTTAAAGCTCAAC | 7874 |
rs369715991 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962679 | ACATCTGCGTTCCTT[A/G]CAGGTATTTTCGAAC | 7874 |
rs369738470 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893753 | TGACAGTTGCCTTGC[A/C]CTGTGGTTACCATAA | 7874 |
rs369744312 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8944914 | GGAGTTCGAGATCAG[A/C]CTGGCCAATATGGCG | 7874 |
rs369790846 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8916071 | GTGATTAGTGATGGC[A/G]CGGGGAGAGTAATCA | 7874 |
rs369795537 | in-del | -/GA | | | intron-variant | USP7 | GRCh38.p7 | 16:8903856 | GGGCAACAAGAGTGA[-/GA]AACTCTGTCTCAAAA | 7874 |
rs369818746 | snp | C/T | 0.000148332 | 0.0086107 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893967 | GGGCCACCCACACAC[C/T]GTCCTCGCCTTGAAC | 7874 |
rs369848741 | snp | A/C | 1.65209e-05 | 0.00287405 | intron-variant | USP7 | GRCh38.p7 | 16:8898517 | CCCATAGTTACATTA[A/C]TTTGGACTCATACCT | 7874 |
rs369885372 | snp | A/G | 1.651e-05 | 0.0028731 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8906501 | ATGAACCAGGACTGC[A/G]TGAAGAATATAATTT | 7874 |
rs369889930 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964366 | TTGGGGTCAGCGCCT[A/G]GAAGTTCCTGTTATT | 7874 |
rs369902549 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8941246 | ATTCCAGAACATGAA[C/G]CTAAGTGGAAAAATT | 7874 |
rs369921676 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8959441 | TAATAATGAGGATAT[C/G]AGCAGCCTGAAAGAA | 7874 |
rs369964364 | in-del | -/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8916987 | AAAAAAAAAAAAAAA[-/G]AGGAAGCAGAATGGC | 7874 |
rs369977152 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8931062 | CATGCAAAGTCATTA[A/T]TTTACTATAGGTTTC | 7874 |
rs369994874 | snp | A/G | 3.33095e-05 | 0.00408089 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8923397 | CTGAAAGGTTGCCTC[A/G]GAGCGCCAACTGGTG | 7874 |
rs370001194 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8959886 | TGCTCCTAATAGCAG[C/G]AGTCTAAGTGTCATA | 7874 |
rs370012942 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | USP7 | GRCh38.p7 | 16:8919807 | CACGACCGTCACCAA[G/T]CGGGACCAGTGCTGG | 7874 |
rs370044222 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8905118 | GACAGAAAAGGATAT[C/T]GGAGATTCATGGTAC | 7874 |
rs370064616 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8911701 | TGAGAGGAGCTCAAG[A/G]GAGCGGGAACCTGCT | 7874 |
rs370070575 | snp | A/G | 5.09074e-05 | 0.00504491 | missense, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8930397 | TCATCTGTATCTCCC[A/G]CTTTAAAGAAGAAAA | 7874 |
rs370095864 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | USP7 | GRCh38.p7 | 16:8913394 | ACAGGAGAGAAGAGA[A/C]GTGAAGTGAAGCGAA | 7874 |
rs370122792 | snp | C/T | 0.000282745 | 0.0118867 | intron-variant | USP7 | GRCh38.p7 | 16:8898658 | CACAAGAAAACAGCA[C/T]ATAAATAAATGACTT | 7874 |
rs370128581 | snp | C/T | 8.47321e-05 | 0.00650837 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8902388 | ATATTTACTGTTTTA[C/T]TGCCGTCGGCTTCAT | 7874 |
rs370152060 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8944076 | ACAAAAAAGGATGAA[C/T]TGGGACAATATCCAT | 7874 |
rs370164816 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8934620 | CGCAAAGCAAGCAGA[C/G]GTCTGCGGTTGCAGC | 7874 |
rs370169727 | snp | C/T | 8.45501e-05 | 0.00650138 | intron-variant | USP7 | GRCh38.p7 | 16:8915205 | TGAAACATTAAAACA[C/T]AGTAGAAATCATCAA | 7874 |
rs370171292 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8913335 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCC | 7874 |
rs370188136 | snp | C/G/T | 8.30812e-05 | 0.00644473 | intron-variant | USP7 | GRCh38.p7 | 16:8904607 | CCCCTGCAGATGGAC[C/G/T]TTCCCCTCTTAGAAG | 7874 |
rs370236209 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8930092 | CCTTGCCTAGGCTAG[C/G]GAGACTCTACTTACC | 7874 |
rs370243930 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8942363 | ATATCAAGCAGTGGG[A/G]TCTGTCCCACCCTTA | 7874 |
rs370249717 | in-del | -/TCA | | | intron-variant | USP7 | GRCh38.p7 | 16:8929891 | GATTCATAGCTATCA[-/TCA]ACTGATATACACCCT | 7874 |
rs370276589 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8945908 | AAGTAAAAATTAAAA[A/C]AAACAACAGCACTGA | 7874 |
rs370287698 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8916290 | GCTAGTATTAAAATT[C/T]AAGCTTCCTCACTTC | 7874 |
rs370299829 | snp | A/G | 8.37977e-05 | 0.00647239 | intron-variant | USP7 | GRCh38.p7 | 16:8920311 | AAAGCTTCTTTCACT[A/G]CAGCACAAAAGACAT | 7874 |
rs370308132 | snp | C/T | 0.00021587 | 0.0103869 | intron-variant | USP7 | GRCh38.p7 | 16:8894673 | AAAACTCCTCCGTTA[C/T]TTCTGTATATCAGCA | 7874 |
rs370405165 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8924043 | TTTTTTCCCACATGA[C/G]TAGTATAAATTGTTA | 7874 |
rs370416755 | snp | A/G | 0.000214269 | 0.0103484 | intron-variant | USP7 | GRCh38.p7 | 16:8905159 | GTCCACCACAGTAAA[A/G]AACAGAACAAAAGTG | 7874 |
rs370448414 | in-del | -/GAGA | | | intron-variant | USP7 | GRCh38.p7 | 16:8932621 | GCTAAATTTAAAAAA[-/GAGA]AAGAAAAGAAAAATC | 7874 |
rs370461743 | snp | A/G | 0.000433584 | 0.0147175 | missense, utr-variant-5-prime, intron-variant | USP7 | GRCh38.p7 | 16:8936609 | AGCCTGTGGTTCCCA[A/G]CCATCTCTGCATGGC | 7874 |
rs370496872 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8903744 | TGGTGGCACATGCCT[A/G]TAATCCCAGCTACTA | 7874 |
rs370510573 | snp | A/G | 0.000153543 | 0.00876059 | intron-variant | USP7 | GRCh38.p7 | 16:8902521 | TTAAAATAAAAACAC[A/G]CTCATATTTTAGTCC | 7874 |
rs370551422 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8955488 | AGCACTTTGGGAGGC[C/T]GAGTGAGGCAGCTCA | 7874 |
rs370579061 | snp | G/T | 9.90213e-05 | 0.00703569 | intron-variant | USP7 | GRCh38.p7 | 16:8899096 | TGCAGTCAAGACCAA[G/T]CAAGTGTCCACACAT | 7874 |
rs370599240 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8896278 | GGCCACATTTGGGCA[A/C]AGAGATGTACAGACT | 7874 |
rs370642985 | snp | C/T | 0.000187811 | 0.00968867 | intron-variant | USP7 | GRCh38.p7 | 16:8923453 | CACAGAGCCTGTGCA[C/T]TGACCAAAAGCACTA | 7874 |
rs370653225 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8905275 | ACCCCCATAATTGTG[C/T]TCAATTGCTTCCTCT | 7874 |
rs370654731 | snp | A/C/T | 4.94942e-05 | 0.00497444 | intron-variant | USP7 | GRCh38.p7 | 16:8901082 | AGAAGATATTTTAAA[A/C/T]GTGTAGCTGTAATGT | 7874 |
rs370655055 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8946533 | ATCTGCAAATCGCGT[A/G]TCTTACAAAGACTCA | 7874 |
rs370658575 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8940337 | CAAGAACCAGAACAC[A/C]GCCAAATGCTCTGGT | 7874 |
rs370659133 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957324 | CTAAAGTAGGTGACA[C/T]TTAACATCTAACTCT | 7874 |
rs370762714 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | USP7 | GRCh38.p7 | 16:8921121 | ACAACAAGCAGTAAT[A/G]CACCAATTGTTCAGA | 7874 |
rs370839269 | snp | C/T | 0.000100895 | 0.00710191 | intron-variant | USP7 | GRCh38.p7 | 16:8910876 | AAGCTTCATTTATAA[C/T]GTAGCCAACACAGGT | 7874 |
rs370881738 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950266 | CAGAGCCTTGGTATC[C/T]AGGCTTGCAGAGTAG | 7874 |
rs370922107 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950617 | TGACAGAGACAACAG[C/T]CTCAGTTACCAACCC | 7874 |
rs371049977 | snp | C/T | 5.40896e-05 | 0.00520018 | intron-variant | USP7 | GRCh38.p7 | 16:8902345 | CTAACGCCTTCTGCA[C/T]GGTTCCAAACCAGAT | 7874 |
rs371100332 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8942335 | TGGGAATCCTGGTAC[C/T]AGCCCTTGCCAAATA | 7874 |
rs371189235 | snp | C/T | 3.30753e-05 | 0.00406652 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8894589 | AATTTACTTCATACT[C/T]GTCTTCATTTATGTA | 7874 |
rs371203875 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8940476 | GCCACCATCAAGGCT[A/G]TTGATCAGAGTGGGA | 7874 |
rs371228636 | in-del | -/TCTGGAGAC | | | intron-variant | USP7 | GRCh38.p7 | 16:8908552 | AACATGTCTGGAGAC[-/TCTGGAGAC]AAAGGCAGGGAAGTT | 7874 |
rs371233731 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961287 | CACCTGAGGTCGGGA[A/G]TTCGAGACCAGCCTG | 7874 |
rs371238922 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8930788 | AGGCTGGCCAACATG[A/G]TGAAACCCCGTCTCT | 7874 |
rs371247084 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | USP7 | GRCh38.p7 | 16:8899109 | AAGCAAGTGTCCACA[A/C]ATGTGACCTACCCTT | 7874 |
rs371248981 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8915090 | CCAACACCAGAGCTG[C/G]GTGGAGGTAACAAGC | 7874 |
rs371261156 | snp | C/T | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8915495 | CCTCTACACAGGTGC[C/T]TTTCATCTTATTTTC | 7874 |
rs371291579 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8942731 | TTCTGTATTTTTTTG[A/T]AGAGACTGGGTCTCA | 7874 |
rs371361168 | snp | G/T | 6.672e-05 | 0.00577543 | intron-variant | USP7 | GRCh38.p7 | 16:8904412 | GCATGGTGACCCGGA[G/T]TCCCAGAAGGGCGGG | 7874 |
rs371368523 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8902648 | TAATCCCAGCACTTT[C/G/T]GGAGGCCGAGGCAGG | 7874 |
rs371403081 | snp | A/G | 0.000115469 | 0.00759743 | intron-variant | USP7 | GRCh38.p7 | 16:8895201 | GCAAGTGATGTGGTC[A/G]AAGTGTCCACATCTC | 7874 |
rs371456257 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP7 | GRCh38.p7 | 16:8945592 | GACTGGGGACATACC[A/G]TGCCCATGGAGTGGG | 7874 |
rs371464982 | in-del | -/AG | | | intron-variant | USP7 | GRCh38.p7 | 16:8913340 | CAGCCTGGGCAACAG[-/AG]CGAGACTCCCTCTCA | 7874 |
rs371469384 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8897724 | AAAAAAAAAAAAAAA[A/T]AAATATATATATATA | 7874 |
rs371547637 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8916119 | CTCAATGAGAACCTC[A/G]CTGCACAGGAGGGGT | 7874 |
rs371562311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8943272 | TTTTAATGCTGTGTT[A/G]TGCACTGAGAGGGGT | 7874 |
rs371640483 | snp | A/G | 0.000148447 | 0.00861404 | intron-variant | USP7 | GRCh38.p7 | 16:8901087 | ATATTTTAAATGTGT[A/G]GCTGTAATGTACTGA | 7874 |
rs371645767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8901689 | TTGTACTGGAAGACA[A/G]CCAGCTCGTTCATTT | 7874 |
rs371652598 | snp | A/C | 4.97352e-05 | 0.00498649 | intron-variant | USP7 | GRCh38.p7 | 16:8930279 | CTGCGAGGCGGTGAA[A/C]CACAGGCACTTACCA | 7874 |
rs371660088 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8934442 | CCAAGATCAATTCAA[A/G]AGCGCATAACATCTT | 7874 |
rs371661228 | snp | A/G | 0.000164829 | 0.00907674 | intron-variant | USP7 | GRCh38.p7 | 16:8905369 | CAGCAGCGATCAAGC[A/G]CTGTGACAAGTACCC | 7874 |
rs371665391 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8958543 | ACAGTTCCAGCATGA[A/G]GCAGCAAGGGCCTGC | 7874 |
rs371671884 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8948248 | GAATGAGTGGCACCA[C/T]CTCAGCTCACTGCAG | 7874 |
rs371676359 | snp | A/C/G | 4.96942e-05 | 0.00498448 | intron-variant | USP7 | GRCh38.p7 | 16:8899576 | TCTGGAGTGGGATCT[A/C/G]AAGAGGAAAGGAGCA | 7874 |
rs371677950 | snp | C/G | 0.000625865 | 0.0176788 | intron-variant | USP7 | GRCh38.p7 | 16:8894878 | GGCAAAGGACATGTG[C/G]TCACACAGTCACTCC | 7874 |
rs371708503 | snp | A/G | 0.00139983 | 0.0264189 | intron-variant | USP7 | GRCh38.p7 | 16:8901124 | TCTACTCAGAAGGTA[A/G]GTGCACGAAGGACTT | 7874 |
rs371711096 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893478 | ACCCGAGGAAGGGCC[A/G]ACAATGCACACAATG | 7874 |
rs371728349 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8927146 | GCCAACATAGTGAAA[A/C]CCCGGCTCTACTAAA | 7874 |
rs371733967 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8951183 | TTGCCACTGTTTGAC[A/T]GCTACAGTCACTTTA | 7874 |
rs371755960 | snp | C/T | 4.96619e-05 | 0.00498282 | intron-variant | USP7 | GRCh38.p7 | 16:8921128 | GCAGTAATGCACCAA[C/T]TGTTCAGACTAAATA | 7874 |
rs371792821 | snp | C/T | 3.30666e-05 | 0.00406598 | intron-variant | USP7 | GRCh38.p7 | 16:8896951 | AGAGGTCAGCGTTAA[C/T]TGCCACCCCTAACTG | 7874 |
rs371809949 | snp | A/G | 9.04805e-05 | 0.00672548 | intron-variant | USP7 | GRCh38.p7 | 16:8895751 | AGCAGCCTGAACAGA[A/G]AGGAAAAAAAAATAG | 7874 |
rs371829601 | snp | A/G | 3.29506e-05 | 0.00405884 | intron-variant | USP7 | GRCh38.p7 | 16:8894768 | GCCAAGCCCCCAGGA[A/G]GCCCCAGCTGCACAC | 7874 |
rs371830715 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8940576 | ATCAGAAAGGGAGAG[C/G]TGGGAGCCTGTAAGC | 7874 |
rs371835065 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | USP7 | GRCh38.p7 | 16:8911287 | CATCTCCCCACCCCC[A/G]CCTGTTCCAGGTGGA | 7874 |
rs371835752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8927037 | AAAGAAAGGTAGGCC[A/G]GGCGCAGTGGCTCAC | 7874 |
rs371842054 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8908598 | CCATTTAGGGCATCT[C/T]TGAAATGTTTTCTTT | 7874 |
rs371857808 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8917814 | TTTGTTTTTGAGACG[C/G]AGTCTTGCTCTGTCA | 7874 |
rs371858977 | snp | C/G/T | 1.68977e-05 | 0.00290665 | intron-variant | USP7 | GRCh38.p7 | 16:8898315 | GGTAGAAACAATAAG[C/G/T]AAGTTCCAATAAAAA | 7874 |
rs371884501 | snp | A/T | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8901147 | AAGGACTTACGTATT[A/T]TACAGGATATTGGTG | 7874 |
rs371916629 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8907195 | AAACGATGCCCAAAT[A/C]TGAACATTTATGTGA | 7874 |
rs371925171 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892333 | TCACACGGGTCACAA[A/G]GCAGCTCTCAGAGCA | 7874 |
rs371990829 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8894911 | GCACCCCCAGGCCAC[A/G]TCACGTGGCAGCCGC | 7874 |
rs372000415 | snp | C/T | 1.64914e-05 | 0.00287149 | intron-variant | USP7 | GRCh38.p7 | 16:8915397 | TAGTCAAAAAATTCA[C/T]ATTCTAAAACCTTTA | 7874 |
rs372059690 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8955704 | AGCACGATTCCATCT[A/C]AAAAAAAAAAAAAAA | 7874 |
rs372119271 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892734 | CCTGTTTCCAGGGAG[A/G]GTAGAAATCTTCCTC | 7874 |
rs372120557 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8940598 | CCTGTAAGCTCCCGA[A/G]GCATCCACAGAAACA | 7874 |
rs372124405 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8943701 | GAACACACTTTTCTA[C/G]AGTCAACTGTCCTTC | 7874 |
rs372148483 | snp | A/G | 3.29484e-05 | 0.00405871 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8899721 | GAAATACTCCTTTGC[A/G]GTGGGTAATTCACTG | 7874 |
rs372182735 | snp | A/C/T | 5.47833e-05 | 0.00523347 | intron-variant | USP7 | GRCh38.p7 | 16:8930423 | GAAAAAGAAATTCCA[A/C/T]GGGTTTTACATTCAT | 7874 |
rs372225595 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8928041 | AAAAATAGTGAATAA[C/G]GAACTAAAAGTAGAA | 7874 |
rs372236149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8934915 | AATGAGTTAGTTCCG[C/T]AAGAGGATTAAAATT | 7874 |
rs372264215 | snp | A/G | 1.64836e-05 | 0.0028708 | intron-variant | USP7 | GRCh38.p7 | 16:8915362 | GCAAATAAGGAAAGT[A/G]AAAGTGGTTTAACTA | 7874 |
rs372283736 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8895930 | CAACCTCCGCCTCCC[A/G]GGTTCAAGCAATTCT | 7874 |
rs372291077 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957787 | AACAAAAAAAAATTA[A/C]AAACACAAAAACGAT | 7874 |
rs372295471 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8940113 | CAAAAAAAAAAGGCT[A/G]TTTCCATCCAGGTTT | 7874 |
rs372411168 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8900822 | GATTCTACAACAGGT[-/A]AAAAAAAAAAAATTC | 7874 |
rs372416049 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | USP7 | GRCh38.p7 | 16:8924839 | ACACTCTTCATCCCA[A/T]ATTATTTTATTTCAC | 7874 |
rs372527770 | snp | C/G | 1.65135e-05 | 0.00287341 | intron-variant | USP7 | GRCh38.p7 | 16:8902053 | ACGCTACTGCTCTAA[C/G]TGCAGGCAGGCGTCT | 7874 |
rs372540383 | snp | A/C | 9.89576e-05 | 0.00703342 | intron-variant | USP7 | GRCh38.p7 | 16:8905140 | TCATGGTACAAATGT[A/C]CAAGTCCACCACAGT | 7874 |
rs372567919 | snp | A/G | 1.82994e-05 | 0.00302479 | intron-variant | USP7 | GRCh38.p7 | 16:8930424 | AAAAAGAAATTCCAC[A/G]GGTTTTACATTCATG | 7874 |
rs372569220 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8912475 | AAAGAAAGAAAAAAG[A/C]AAATAAACATTACCA | 7874 |
rs372580025 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8960089 | GGGCAGAGACCCATG[C/G]AAGTCACTCCTTCAG | 7874 |
rs372624562 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8927878 | GGCCAAGTGCAATGG[G/T]TCATGCCTATAATCC | 7874 |
rs372628046 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956910 | TGCCCAGCCCTTCTG[C/G]GCAGCACAACACAGA | 7874 |
rs372636693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8913225 | GCTGGGCATGGTGGC[A/G]CATGCCTCTAATCCC | 7874 |
rs372645978 | snp | A/G | 1.68049e-05 | 0.00289865 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8920443 | TTCTCAGGATCGGTC[A/G]CTTCCTATAAAACAT | 7874 |
rs372663824 | snp | G/T | 3.2956e-05 | 0.00405918 | intron-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894124 | TGGGGATGAAGAAAA[G/T]CAAGTGAGGCCACAG | 7874 |
rs372674528 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8949193 | TATTTTAAAAATCAT[A/G]ATTGTTACCGAATTT | 7874 |
rs372680592 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8938734 | AAAAATTGGGGGGAC[A/G]GGGGAGTCTGTACCA | 7874 |
rs372686526 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8920873 | CCACTCAGTACTATG[A/C]CTGAATCATGAAAGG | 7874 |
rs372710211 | snp | C/G | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8905245 | GCAGTGTCGAACAGA[C/G]AGGTCGTCATCGTGA | 7874 |
rs372724392 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8918034 | TGACCTCATGATCCG[A/C/T]CCGCCTCGGCCTCCC | 7874 |
rs372726209 | snp | A/G | 1.65108e-05 | 0.00287317 | intron-variant | USP7 | GRCh38.p7 | 16:8901062 | GAGCAAGTCACCTAG[A/G]AGAAAGAAGATATTT | 7874 |
rs372751626 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8965305 | AATCCCAGCACTTTG[A/G]GAGGCCAAGGCGGGC | 7874 |
rs372838723 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8958423 | AGGCAGGACACCAAG[A/T]CCTTTTCAGCAAGGC | 7874 |
rs372854684 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8904304 | CTGACCTGCACTTGC[C/G]TACAGAGATGGATGC | 7874 |
rs372907918 | snp | A/C | 0.00049538 | 0.0157304 | intron-variant | USP7 | GRCh38.p7 | 16:8906591 | TTCAAACCTATTAGA[A/C]AACATTTTAAAAGAA | 7874 |
rs372916610 | snp | C/T | 1.66324e-05 | 0.00288374 | intron-variant | USP7 | GRCh38.p7 | 16:8930272 | CCGCCCACTGCGAGG[C/T]GGTGAACCACAGGCA | 7874 |
rs372944160 | snp | A/G/T | 1.64751e-05 | 0.00287007 | intron-variant | USP7 | GRCh38.p7 | 16:8894990 | CCACTCAAAGGCTCC[A/G/T]GGTTTTGACGTGAGC | 7874 |
rs372992267 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8923580 | AAGACTGAGATAACA[C/T]ACAGTTTCTGAATGG | 7874 |
rs373006219 | snp | C/G/T | 7.12733e-05 | 0.00596922 | intron-variant | USP7 | GRCh38.p7 | 16:8923428 | TCTGCAAAAAAAACA[C/G/T]ATCATCAGTCACAGA | 7874 |
rs373087684 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8917900 | GTCCACGCCATTCTC[C/T]TGCCTCAGCCTCCCC | 7874 |
rs373089638 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8910107 | TTAATTATAAATTAG[C/T]TGAGTCAATGAGTCA | 7874 |
rs373148407 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8933588 | TTTCTTCACTGTATA[C/T]GCACACACTCACACT | 7874 |
rs373219567 | snp | C/T | 0.000131867 | 0.00811889 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8917133 | AGACGAATCATCCCC[C/T]TCGGTTGGCATCATG | 7874 |
rs373277930 | in-del | -/C | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961508 | AAAAAAAAAAAGGGG[-/C]GGGGGGGGCAAATAC | 7874 |
rs373323625 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8952903 | GTGCACTGGCGCAAT[C/G]TCGGCTCACTGCAAC | 7874 |
rs373361967 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8909565 | CAGACCCTAAAACAT[C/G]CAGAATAGAGAACAG | 7874 |
rs373405897 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8936131 | ACCAGGTGGTGCCTT[C/G]TCCATGAAGACCCAG | 7874 |
rs373432556 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8897673 | TCAAGACCAGTCTGG[A/G]CAATATAGTGAGACC | 7874 |
rs373443625 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8900420 | TTACATTAAAAAAAA[C/G]AAAAACAAAAACGTG | 7874 |
rs373482138 | in-del | -/A | 0.00141047 | 0.0265188 | intron-variant | USP7 | GRCh38.p7 | 16:8894648 | AATTTAAACTAAAAG[-/A]AAAAAAATTAAAACT | 7874 |
rs373524090 | snp | C/T | 4.95683e-05 | 0.00497812 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8898576 | AGGCTTGAAGAACTG[C/T]AGAAGATCTCTTAAA | 7874 |
rs373532980 | snp | A/G | 3.31598e-05 | 0.00407171 | intron-variant | USP7 | GRCh38.p7 | 16:8901248 | ATCTACAAGGTTAAT[A/G]AACAAGTTTTGTTAA | 7874 |
rs373533776 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8952783 | CTAGTCACAGAGTCT[A/G]GCAGTTCCCAAACTC | 7874 |
rs373547298 | snp | A/C/G | 9.90122e-05 | 0.00703543 | intron-variant | USP7 | GRCh38.p7 | 16:8896977 | AACTGAACGTCCACA[A/C/G]TTGGGCTCAAGAAAT | 7874 |
rs373610737 | snp | A/C | 0.00016497 | 0.00908063 | intron-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894154 | GAGCAGCCCTGGAAC[A/C]CCTCAGCGGGGTGGT | 7874 |
rs373612996 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893683 | CCACTAGGGACAGCC[C/T]AGAGACCTTGAGCCA | 7874 |
rs373648408 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8915583 | TAGTAATATATACAG[C/T]AATTTTATAATTGAC | 7874 |
rs373696932 | snp | A/G/T | 9.89045e-05 | 0.00703161 | intron-variant | USP7 | GRCh38.p7 | 16:8899804 | CAAAGTCCATGGCAG[A/G/T]GGGTAGCTGGTAAAA | 7874 |
rs373719410 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8931863 | CTGCAACTAATGCTG[G/T]CCCCACGGTTGCCTA | 7874 |
rs373742305 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8930214 | CCAAGGATGTACCCA[A/G]GAAGTACCAAGCATG | 7874 |
rs373752319 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8913693 | TTAAAAACGGAGGAG[C/T]ATTGCAAGCTGTAAA | 7874 |
rs373760995 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8914388 | ATCAAGCTGGACATA[A/C]GCACACCCTACAGGC | 7874 |
rs373845335 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8940641 | GCAGCCAAAAAAGAC[A/G]GAGTTACCACACTCC | 7874 |
rs373890669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8949336 | GACATAAAAATGCAA[C/T]GCAATTGATTGTTGG | 7874 |
rs373907861 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8934516 | TTCAGCAGTGGGATT[A/T]ATTGCAGTGTGATGA | 7874 |
rs373919497 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8958973 | CATAGCACCCATCTT[C/T]GATGGCCCCACCTGT | 7874 |
rs373928132 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8948680 | GACTACTGGCTACGA[C/T]GTGGATGAACCTTGA | 7874 |
rs373931498 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8920434 | ATAAATCCTTTCTCA[A/G]GATCGGTCACTTCCT | 7874 |
rs373992565 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8936148 | CCATGAAGACCCAGC[G/T]CGGCCTCTGAGCCAC | 7874 |
rs374020920 | snp | A/G | 0.0327613 | 0.123723 | synonymous-codon, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8963226 | CATCTCCATGTCCTC[A/G]GGCTCGCTCAACTGC | 7874 |
rs374065624 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950440 | TCTGATTTCCAAAGG[A/C]AATACTGATCATTAA | 7874 |
rs374075093 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8920756 | TGCAATGATAAGTGA[A/C]TTAGCATAGTAAGAA | 7874 |
rs374121025 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8954989 | AATAAAAAAACAGTA[A/G]CAGCAATTGCTGTTT | 7874 |
rs374148565 | in-del | -/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8903004 | AAAGAGGGGGTAGGG[-/G]TGCAGGGAGTGGAGT | 7874 |
rs374178138 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8906164 | CATTCAGAAGAAAAT[A/G]TAAGTGTCTCATATG | 7874 |
rs374207468 | snp | C/T | 3.2962e-05 | 0.00405954 | missense, intron-variant | USP7 | GRCh38.p7 | 16:8904542 | GAGGAATATCATGGT[C/T]GGTGACCGCCTGTAA | 7874 |
rs374207629 | snp | C/T | 3.29451e-05 | 0.00405851 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8895052 | TATCCTCAGCAAAAA[C/T]GGGATTCCGAACGTT | 7874 |
rs374224337 | snp | G/T | 6.72529e-05 | 0.00579844 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8902461 | GCATGGGCCACAATC[G/T]AATTTGATCTTGTGG | 7874 |
rs374270681 | in-del | -/GTTT | | | intron-variant | USP7 | GRCh38.p7 | 16:8908636 | TTTATGGGTCTCTTT[-/GTTT]ATTAAAATAATGCTG | 7874 |
rs374270832 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | USP7 | GRCh38.p7 | 16:8920465 | ATAAAACATAAATAA[G/T]AATATCCAGCTTGAA | 7874 |
rs374276830 | snp | A/G | 0.000117309 | 0.00765772 | intron-variant | USP7 | GRCh38.p7 | 16:8904393 | TAGAGATGGGTGCCC[A/G]GCTGCATGGTGACCC | 7874 |
rs374315435 | snp | C/G | 3.29707e-05 | 0.00406008 | intron-variant | USP7 | GRCh38.p7 | 16:8895167 | TGGGGACACGGACAA[C/G]AGACACAGTTCTGTA | 7874 |
rs374321309 | snp | A/G | 1.64882e-05 | 0.00287121 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8903355 | CACTTTTTCTTCATC[A/G]TACATGTCATTCCCT | 7874 |
rs374324826 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP7 | GRCh38.p7 | 16:8953206 | CTCCCCCTCCCCGCG[A/G]TAAGCCAGTCCTGTC | 7874 |
rs374329334 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8946381 | TGGCCAGGAGTTCAA[G/T]ACCAGCCTGGCCAAT | 7874 |
rs374329816 | snp | A/G | 1.64936e-05 | 0.00287168 | intron-variant | USP7 | GRCh38.p7 | 16:8895630 | GGTGCCAACAGTATC[A/G]GGGACAGATACCTCT | 7874 |
rs374372094 | snp | A/G | 0.000182759 | 0.00955752 | intron-variant | USP7 | GRCh38.p7 | 16:8917170 | GCCTGAAACAATTAA[A/G]AAATAAGAATTTTTA | 7874 |
rs374382443 | in-del | -/A | 0.0158469 | 0.0875917 | intron-variant | USP7 | GRCh38.p7 | 16:8913050 | AAACCAGTGAGAAGG[-/A]AAAAACCTTAAAAGC | 7874 |
rs374403655 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8942764 | ATGTTGTCCAGGCTG[A/G]TCTTGAACTCCTGGC | 7874 |
rs374435568 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961537 | ACCTTGAAATTTGTG[A/G]ACCTGGTCATTTTCC | 7874 |
rs374447881 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892329 | TCTATCACACGGGTC[A/T]CAAGGCAGCTCTCAG | 7874 |
rs374474942 | in-del | -/GAAAC | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892630 | AAAAAAAAAAAAAAA[-/GAAAC]AAGAGACCCTGCCCC | 7874 |
rs374478291 | snp | A/C/G | 4.96852e-05 | 0.00498403 | intron-variant | USP7 | GRCh38.p7 | 16:8921123 | AACAAGCAGTAATGC[A/C/G]CCAATTGTTCAGACT | 7874 |
rs374486766 | snp | A/C/G | 0.00011563 | 0.00760288 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8899141 | AGACTTGAAAAACTG[A/C/G]AGCAACATTGGATCT | 7874 |
rs374697578 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8945698 | TCATAGCTAAGGACA[A/C]GCTGATTCTAATATT | 7874 |
rs374703185 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8916126 | AGAACCTCGCTGCAC[A/G]GGAGGGGTCTGGACA | 7874 |
rs374706858 | snp | A/C | 3.29522e-05 | 0.00405894 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893982 | CGTCCTCGCCTTGAA[A/C]ACACCAGCTTGGAAA | 7874 |
rs374711236 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8892228 | CAAACCCACAGCGAA[C/T]GGCTCTCGCACCCCT | 7874 |
rs374719078 | snp | C/G/T | 0.00021804 | 0.0104391 | intron-variant | USP7 | GRCh38.p7 | 16:8903220 | GACACGGAAGGAAGG[C/G/T]GGACGTTGGGAGCCA | 7874 |
rs374784693 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8916020 | TGTGTGTGCTTCTGC[A/G]TCTTTTATCACAACT | 7874 |
rs374841349 | snp | C/T | 6.60557e-05 | 0.0057466 | intron-variant | USP7 | GRCh38.p7 | 16:8916467 | GCTTCAAAATATTCA[C/T]TGTAAGAAATATACA | 7874 |
rs374895416 | snp | A/G | 0.000100834 | 0.00709976 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8902458 | CTTGCATGGGCCACA[A/G]TCGAATTTGATCTTG | 7874 |
rs374977170 | snp | A/G | 3.32055e-05 | 0.00407451 | intron-variant | USP7 | GRCh38.p7 | 16:8915248 | TTAGATACACACAAC[A/G]CTTACTATTTTTCTT | 7874 |
rs375038883 | snp | A/C/T | 0.000155136 | 0.00880614 | intron-variant | USP7 | GRCh38.p7 | 16:8921324 | TAATCTGAGCCTTAG[A/C/T]TGACATTATTTACCA | 7874 |
rs375075563 | snp | A/C | 0.000691973 | 0.0185878 | intron-variant | USP7 | GRCh38.p7 | 16:8894897 | CACAGTCACTCCCAG[A/C]ACCCCCAGGCCACGT | 7874 |
rs375115068 | snp | C/G | 3.30513e-05 | 0.00406504 | intron-variant | USP7 | GRCh38.p7 | 16:8898465 | GAAAGATTCACATCA[C/G]ATACCGTCACCAAAA | 7874 |
rs375139030 | snp | A/G | 0.000188891 | 0.00971646 | intron-variant | USP7 | GRCh38.p7 | 16:8902525 | AATAAAAACACGCTC[A/G]TATTTTAGTCCTCTA | 7874 |
rs375140095 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8907341 | TTTCTGGCTGAGACA[C/G]TTTCTGACCACGGTA | 7874 |
rs375140436 | snp | A/G | 1.64947e-05 | 0.00287177 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8906471 | CACATAATGTCCACC[A/G]TGATTATCTCCACTA | 7874 |
rs375194813 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8927534 | ATCCATCTAGATCTT[C/T]AGAGGCCGTATTTGC | 7874 |
rs375197014 | snp | A/G | 1.64969e-05 | 0.00287196 | intron-variant | USP7 | GRCh38.p7 | 16:8901085 | AGATATTTTAAATGT[A/G]TAGCTGTAATGTACT | 7874 |
rs375320194 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | USP7 | GRCh38.p7 | 16:8894915 | CCCCAGGCCACGTCA[C/T]GTGGCAGCCGCCAAA | 7874 |
rs375330302 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8952433 | TGAAATGGGTCTCAC[C/T]GGGCTAAAACCAAGG | 7874 |
rs375358412 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956935 | CACAGACAAGTCGAC[A/G]CTATCTCTCAGGGTG | 7874 |
rs375387587 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8952003 | ACTGGGAAGCCCAAC[G/T]GCAGTTCACGACTTT | 7874 |
rs375403153 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950646 | CCAGCCCTGTCTGCC[A/G]CGAACATGGCACTGC | 7874 |
rs375455699 | snp | C/T | 8.23798e-05 | 0.00641741 | intron-variant | USP7 | GRCh38.p7 | 16:8919024 | GAGAGGAACACTATC[C/T]ATTTACCTTTCGTAG | 7874 |
rs375459178 | snp | C/T | 0.000216125 | 0.0103931 | intron-variant | USP7 | GRCh38.p7 | 16:8901258 | TTAATAAACAAGTTT[C/T]GTTAAGATCCAAACA | 7874 |
rs375499593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8936024 | CCACTTCACGAAGAT[C/T]TATCAATCCTCCCCC | 7874 |
rs375539685 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8953678 | CCGTGCGGCGCCACC[G/T]GAGGCAGAGGGAAGA | 7874 |
rs375547032 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8941427 | CCTAATACGTTACTT[A/T]TCCAGACAGGAAGGA | 7874 |
rs375578803 | in-del | -/A/AAA | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956776 | TAAAAAAACAAAAAC[-/A/AAA]AAAAAAAAAAAAACA | 7874 |
rs375579449 | snp | C/G | 1.64819e-05 | 0.00287066 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893966 | GGGGCCACCCACACA[C/G]CGTCCTCGCCTTGAA | 7874 |
rs375580884 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8952812 | TCATCCTGCTATTCC[A/C]CCCCTCCCGCCTGTG | 7874 |
rs375585751 | snp | C/T | 0.00131967 | 0.0256534 | intron-variant | USP7 | GRCh38.p7 | 16:8896972 | CCCCTAACTGAACGT[C/T]CACAATTGGGCTCAA | 7874 |
rs375615113 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893295 | TGCCAAGGCAGCAGA[C/G]TAAACCTTAATTGAA | 7874 |
rs375620500 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8934179 | ATGCAAAAATGAGGG[C/T]TCATTTTCTGTACAT | 7874 |
rs375623311 | snp | A/G | 3.29919e-05 | 0.00406138 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8930327 | CGCGGTGTTGTGTCC[A/G]TCACTCAGGGCCACA | 7874 |
rs375640158 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8952815 | TCCTGCTATTCCACC[C/T]CTCCCGCCTGTGACC | 7874 |
rs375664275 | in-del | -/C | | | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962446 | GTGCCTTGGAAAATT[-/C]ACTGCCACATCGGCA | 7874 |
rs375688404 | snp | C/T | 0.0193772 | 0.0965046 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8965041 | AATGGAGCAAACCGA[C/T]ATACATTTCTACACA | 7874 |
rs375688782 | snp | A/C/T | 3.5968e-05 | 0.0042406 | intron-variant | USP7 | GRCh38.p7 | 16:8902339 | AGAGGACTAACGCCT[A/C/T]CTGCACGGTTCCAAA | 7874 |
rs375725766 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8913304 | GAGGTTGCAGTGAGC[C/T]GAGATCGCACCACTG | 7874 |
rs375728638 | in-del | -/GTCAGGGAAAGA | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8951268 | TAATCTTTAAAATCT[-/GTCAGGGAAAGA]GGCCTCTTAAGTCAC | 7874 |
rs375740069 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8940353 | GCCAAATGCTCTGGT[A/G]AGCTCCAGCACAGGA | 7874 |
rs375813653 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8913401 | AGAAGAGAAGTGAAG[C/T]GAAGCGAAGCGAAGA | 7874 |
rs375822619 | snp | A/G | 3.34052e-05 | 0.00408674 | intron-variant | USP7 | GRCh38.p7 | 16:8900636 | GTTTAACTTCCTACA[A/G]TGAAAGATATAAAAT | 7874 |
rs375864487 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8910786 | ATTTATTGTCCCCAT[C/G]GAGCTGTTCTACTGC | 7874 |
rs375866164 | snp | C/T | 0.00393423 | 0.0441773 | intron-variant | USP7 | GRCh38.p7 | 16:8894720 | CAAAAAAGCCTAGGC[C/T]GCTACGCTAGGCAAG | 7874 |
rs375868816 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960240 | AACATGCAACTGGCT[C/G]CTTCAGGCCTTACAG | 7874 |
rs375937937 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8920994 | AAAGCTGCTAAAAAC[A/G]TAAGATACGAAACTG | 7874 |
rs375949143 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8954433 | GTTCTCAAACTCATC[A/G]TATGAGGCGTGACTG | 7874 |
rs375970067 | snp | A/G | 3.29457e-05 | 0.00405854 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8905257 | AGACAGGTCGTCATC[A/G]TGACCCCCATAATTG | 7874 |
rs375995511 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8926973 | TTGTTACAGCAATTT[C/T]ATCCTCCCAGGGCAA | 7874 |
rs376004573 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8947699 | AAATAACAGTAGCTA[C/T]AACCCACCCACCAAA | 7874 |
rs376025418 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | USP7 | GRCh38.p7 | 16:8901072 | CCTAGGAGAAAGAAG[A/G]TATTTTAAATGTGTA | 7874 |
rs376063186 | snp | A/G | | | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8923229 | CGTGGAATCAGATTC[A/G]GCATTGCACTGGAGA | 7874 |
rs376085871 | in-del | -/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8923204 | CTTCCAGTAATGAAA[-/T]ACTGTCTTACGTGGA | 7874 |
rs376102750 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892507 | CGCCCCGAAGGGCCT[C/T]GTGACACATCAGGTC | 7874 |
rs376151871 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956825 | GCCACAGGCACAGGA[C/T]AGTAAGAGCCCAGCC | 7874 |
rs376218763 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8923639 | TCAGAGTGCTAACCA[C/T]ACACTTGCCATCCCT | 7874 |
rs376232889 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8935938 | TAGACCACTTCAGCA[A/C]GCGAATCTAACCCCT | 7874 |
rs376237187 | snp | C/G | 0.000217801 | 0.0104333 | intron-variant, missense | USP7 | GRCh38.p7 | 16:8894534 | CACCAGCCCCCGGGG[C/G]GGGGAGAACCCTTAC | 7874 |
rs376237235 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8940478 | CACCATCAAGGCTGT[C/T]GATCAGAGTGGGAGG | 7874 |
rs376242543 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8926725 | AATTAGCACTTCATG[A/C]ACAAAGACTCCAATC | 7874 |
rs376259552 | snp | C/T | | | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962717 | CGACGCTAGGCAGTG[C/T]TGTTAGAAAGTGATT | 7874 |
rs376266614 | snp | C/T | 1.64876e-05 | 0.00287116 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8895663 | TCGAAACGTCCGGCT[C/T]GTTGCAGGAGATAAA | 7874 |
rs376287612 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8918921 | GCAGCCATCTGAGGA[A/G]ACAGGGCCAGGGGAG | 7874 |
rs376292439 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8901728 | TTTGTGGCCGCCTTA[C/G]TACAGACAGAAAGGC | 7874 |
rs376341039 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8910543 | CTGCTGGATGTGCTT[C/G]TACAGGATAAACCAG | 7874 |
rs376345647 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8953383 | TGAATGAAAGCCTAC[A/C]CCAGCCTCTGTGGAC | 7874 |
rs376408721 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8941532 | GTCCAGTAACTTGTC[C/G]TAAGCCAAAACACAT | 7874 |
rs376512834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8951726 | TCAGGCCTTTTCACA[C/T]TTAAATCTCTCCATA | 7874 |
rs376520206 | snp | A/G | 1.82161e-05 | 0.0030179 | intron-variant | USP7 | GRCh38.p7 | 16:8930422 | AGAAAAAGAAATTCC[A/G]CGGGTTTTACATTCA | 7874 |
rs376528175 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8898296 | TTTTCAATGTCTGGG[G/T]ACAGGTAGAAACAAT | 7874 |
rs376534252 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938554 | CGTCTCTACTGAAAA[C/T]ACAAAAACTTAGCTG | 7874 |
rs376595760 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8901194 | GTAATTCAAGCTCCG[C/T]GTTTTGGGATCATAC | 7874 |
rs376615993 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893571 | AGGTCATTGAAAGTA[C/T]AACTGAAGGAAATAG | 7874 |
rs376630962 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893115 | AATATACAATTCATT[C/T]TTCCTTTTTTTTTCA | 7874 |
rs376635989 | in-del | -/TAATATACAGCACAAGTAAAGAGCTTATAATTACGCCTGTACTGCTTCTACATGTATAGTCTGCTCCGCAAAAGAAACAGGATTATCTGCTCAACTGTGCAGCACAATGCAAGTAGAAGTT | | | intron-variant | USP7 | GRCh38.p7 | 16:8943289 | GCACTGAGAGGGGTT[lengthTooLong]GCAGCACGCACGGCC | 7874 |
rs376640584 | snp | C/G/T | 0.000131789 | 0.00811661 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8923346 | CGGAGGGCTAAGGAC[C/G/T]GACTCACTCAGTCTG | 7874 |
rs376660235 | snp | C/G | 0.000437904 | 0.0147905 | intron-variant | USP7 | GRCh38.p7 | 16:8899246 | AAACTTGGTCATAAA[C/G]TTCATGCTTAATTAC | 7874 |
rs376682611 | snp | G/T | 1.66988e-05 | 0.00288949 | intron-variant | USP7 | GRCh38.p7 | 16:8899235 | GGGAAAAATTGAAAC[G/T]TGGTCATAAACTTCA | 7874 |
rs376716342 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8897103 | TAGTGTTATTTCCTA[A/G]GTAATGAAAAGATAA | 7874 |
rs376718623 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8935497 | ATTACAGGCGTGGGC[A/C]ACCATGCCCAGGCTA | 7874 |
rs376718767 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8918588 | GCTGAGGCAGGTGGA[C/T]AGCTTGGGGTCAGGA | 7874 |
rs376759701 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | USP7 | GRCh38.p7 | 16:8902031 | AGAACAACAATCCAG[A/G]AATCCAACGCTACTG | 7874 |
rs376769160 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8896047 | TCACCATGTTGGTTA[A/G]CCAGGATGGTCTCGA | 7874 |
rs376771943 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8948627 | AAATCATGGTGAAGT[G/T]CCACACGATGGAATA | 7874 |
rs376772033 | snp | A/T | 1.64792e-05 | 0.00287042 | intron-variant | USP7 | GRCh38.p7 | 16:8901129 | TCAGAAGGTAAGTGC[A/T]CGAAGGACTTACGTA | 7874 |
rs376829358 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957864 | TTATGAAAGTCTATC[A/G]ATGTCTTTGTCTGGA | 7874 |
rs376853622 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8931546 | ATTATGTAAAGATCC[A/G]GGAAAGTGTTTAGGA | 7874 |
rs376871892 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8955851 | CTGTGGAGTAGAAAG[G/T]TTTGCTCAGCCTACA | 7874 |
rs376934036 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8924847 | CATCCCAAATTATTT[G/T]ATTTCACATAACCCT | 7874 |
rs376953697 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957365 | ATGGCAAGAAATATG[C/T]TGTTACAACTCTTGT | 7874 |
rs376979165 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP7 | GRCh38.p7 | 16:8929864 | ATTTCATCCCTAACA[A/G]GAGCGGGGAGGGATT | 7874 |
rs376981126 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8945819 | ACTTTAGGAAGCCAA[C/G]GCAAGAAGACTGCTT | 7874 |
rs377008537 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938051 | GGTAAGGCAGGGCAG[A/C]ATATCCTCCCTATGT | 7874 |
rs377045597 | snp | C/G | 3.2956e-05 | 0.00405918 | intron-variant | USP7 | GRCh38.p7 | 16:8899789 | GTTTGCAGTCTGAAT[C/G]AAAGTCCATGGCAGG | 7874 |
rs377071417 | in-del | -/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8918561 | ATGCCTATAATCTGA[-/G]CCCCTTGGGAAGCTG | 7874 |
rs377089266 | snp | C/T | 0.000197668 | 0.00993955 | intron-variant | USP7 | GRCh38.p7 | 16:8895010 | TTGACGTGAGCCACT[C/T]GGCCAACCACAACAG | 7874 |
rs377095645 | snp | C/G | 4.94352e-05 | 0.00497143 | intron-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894128 | GATGAAGAAAAGCAA[C/G]TGAGGCCACAGAGCA | 7874 |
rs377131617 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8928533 | CTTATCCCCTGAAGA[A/T]GAGGATTGCGCAATT | 7874 |
rs377138187 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891853 | TCACGCAGTGGTTTT[C/T]AGGGCTCCCCGCTGT | 7874 |
rs377146964 | snp | A/G | 0.000136984 | 0.00827485 | intron-variant | USP7 | GRCh38.p7 | 16:8920461 | TCCTATAAAACATAA[A/G]TAAGAATATCCAGCT | 7874 |
rs377154921 | snp | C/T | 8.25607e-05 | 0.00642445 | intron-variant | USP7 | GRCh38.p7 | 16:8919179 | GGGATCTTGCAGATA[C/T]CCCATTGCTCCTGCA | 7874 |
rs377156344 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8929020 | CTCCGCCCTATATCT[A/C]TGTCTCCTCCCAAGA | 7874 |
rs377197195 | snp | A/G | 4.94605e-05 | 0.0049727 | intron-variant | USP7 | GRCh38.p7 | 16:8895174 | ACGGACAACAGACAC[A/G]GTTCTGTAAGTGCAA | 7874 |
rs377239396 | snp | A/G | | | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8904453 | CACTTGCATATAGAG[A/G]TGGGCTTCCTGCCGC | 7874 |
rs377280121 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8896675 | TGTTTGGCTTTTCTA[C/T]GGGAACTGCGCCTTT | 7874 |
rs377304790 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8895856 | TTTTTTTTTTTTTTT[A/T]GAGACAGTCTCAATC | 7874 |
rs377317970 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8918163 | TAAATGTGACTAGAA[C/T]TACCCATGCTGAGCT | 7874 |
rs377382415 | snp | C/T | 3.30055e-05 | 0.00406222 | intron-variant | USP7 | GRCh38.p7 | 16:8902207 | TTCCAAAAGAGACGC[C/T]GATTTTAGAAGAGTC | 7874 |
rs377405622 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | USP7 | GRCh38.p7 | 16:8910847 | AAAGAGAGAGAGAGA[A/G]AAGTCAAGTGCTAAA | 7874 |
rs377464694 | snp | C/G/T | 5.00441e-05 | 0.00500199 | intron-variant | USP7 | GRCh38.p7 | 16:8930264 | ACAAGTTTCCGCCCA[C/G/T]TGCGAGGCGGTGAAC | 7874 |
rs377514317 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8911638 | TGCTGAAAGTTTACA[A/G]GCTGCAGCCCGGAGA | 7874 |
rs377515705 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8916902 | ACACGATTAAATGCT[C/T]AAGCCTCCCTAAATT | 7874 |
rs377597905 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8928490 | ACATATCCAACTTCC[C/T]AGAATCCTGTGCATT | 7874 |
rs377600131 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8913697 | AAACGGAGGAGCATT[A/G]CAAGCTGTAAATATG | 7874 |
rs377602457 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893724 | ATCCACTAACCTCTT[C/T]TCCCCCATTGCGCTG | 7874 |
rs377627909 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8942020 | AGAGTGGCAAATTCT[C/G]TGGCAAGCACAGAGT | 7874 |
rs377644766 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8954234 | CCACTGGAGGCAGAG[C/G]GAAGACACGTGCCCC | 7874 |
rs377685035 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | USP7 | GRCh38.p7 | 16:8898488 | CACCAAAACCCCGAG[A/C]CTTCTCTTTATGACC | 7874 |
rs377690212 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8895097 | GTGGAAATGCGCCAC[C/T]GTGACAAGCATCTCA | 7874 |
rs377691070 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | USP7 | GRCh38.p7 | 16:8895171 | GACACGGACAACAGA[C/T]ACAGTTCTGTAAGTG | 7874 |
rs377694607 | snp | A/C/G | 1.64909e-05 | 0.00287144 | intron-variant | USP7 | GRCh38.p7 | 16:8895186 | CACAGTTCTGTAAGT[A/C/G]CAAGTGATGTGGTCA | 7874 |
rs377731403 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8954462 | TGCATTCGGGTCATG[C/G]GCAATGGGACCACAA | 7874 |
rs377745777 | snp | A/G | 7.20643e-05 | 0.00600225 | intron-variant | USP7 | GRCh38.p7 | 16:8902346 | TAACGCCTTCTGCAC[A/G]GTTCCAAACCAGATA | 7874 |
rs386384178 | in-del | -/AA | | | intron-variant | USP7 | GRCh38.p7 | 16:8955725 | AAAAAAAAAAAAAAA[-/AA]ACATTGCACAGGGTC | 7874 |
rs386384179 | in-del | -/GG | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961505 | TCAAAAAAAAAAAAG[-/GG]GGGGGGGGGGGCAAA | 7874 |
rs386384180 | in-del | -/GG | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961515 | AAAAGGGGGGGGGGG[-/GG]GCAAATACCTTGAAA | 7874 |
rs386788731 | multinucleotide-polymorphism | AG/CC | | | intron-variant | USP7 | GRCh38.p7 | 16:8910198 | AACAGACCAGCCAGA[AG/CC]AGCAGCCAGAAACAG | 7874 |
rs386788732 | multinucleotide-polymorphism | CT/GG | | | intron-variant | USP7 | GRCh38.p7 | 16:8933969 | ACCATGTTGGCCAGG[CT/GG]GGTCTCAAACTCATG | 7874 |
rs386788733 | in-del | ACTG/TC | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956791 | CAAAAAAAAAAAAAC[ACTG/TC]AATTTGCTTTACACA | 7874 |
rs386788734 | multinucleotide-polymorphism | CA/TG | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957496 | CACCTATAATCCCAG[CA/TG]CTTTGAGAGGTTCAG | 7874 |
rs386788735 | multinucleotide-polymorphism | GA/TG | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961221 | ACACCGGCCAGGCGC[GA/TG]TGGCTCACACCTGTA | 7874 |
rs386788736 | multinucleotide-polymorphism | CTG/GTA | | | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962683 | CTGCGTTCCTTGCAG[CTG/GTA]TTTTCGAACGTAAGC | 7874 |
rs397790264 | in-del | -/A | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938352 | TCAAAAAAAAAAAAA[-/A]GAAAGAAAGAAAGAA | 7874 |
rs397944005 | in-del | -/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8896915 | GATCCCAGCTGGGTG[-/G]ATTTCCACCAACGCA | 7874 |
rs397944053 | in-del | -/A | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938723 | TCAAAAAAAAAAAAA[-/A]TTGGGGGGACGGGGG | 7874 |
rs397946815 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8904792 | TACTAAAAAAAAAAA[-/A]TAAAATAAAAATAAA | 7874 |
rs397966580 | in-del | -/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8944905 | TGAGGTCAGGAGTTC[-/C]GAGATCAGCCTGGCC | 7874 |
rs398028682 | in-del | -/A | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8901332 | AACGAAAAAAAAAAA[-/A]CAGTAAGCTGAATAG | 7874 |
rs398028683 | in-del | -/A | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8926168 | CAAAAAAAAAAAAAA[-/A]GAAAATTTCACTAAA | 7874 |
rs398028684 | in-del | -/A/AAG/AG | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8959370 | CAAAAAAAAAAAAAA[-/A/AAG/AG]GGATACCTTCTTCCT | 7874 |
rs398078486 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8959369 | TCAAAAAAAAAAAAA[-/A]AGGATACCTTCTTCC | 7874 |
rs527283300 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8924987 | CCTTTTGAGGATAGA[A/C]GTCTACTAAAAGGCA | 7874 |
rs527291222 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8909217 | TGCCTATCTCGACCA[C/T]GGCCAGGCGGTCAGG | 7874 |
rs527304738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8952231 | TTCCAGCCTGGGCAC[A/G]AGGGAGAGCCTGTCT | 7874 |
rs527311736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8924567 | TGTAGGCTTGGGTAA[A/G]GAGTGCCTAAGAACA | 7874 |
rs527363958 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8922667 | GTGGTCCGTACTCCC[A/G]GAATCAACTGGGTTT | 7874 |
rs527382597 | snp | A/C/T | 8.34319e-05 | 0.00645832 | intron-variant | USP7 | GRCh38.p7 | 16:8915539 | AACTGAAAAAGAATG[A/C/T]TTTGGCTTTAAAAAA | 7874 |
rs527419545 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8946748 | CACAGCCACTCACGC[G/T]CAACCACTCAGCCAT | 7874 |
rs527455851 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8943435 | CGGCCGGAACCGAGC[C/T]GCACAGATGCAGTTA | 7874 |
rs527494684 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8943028 | AAGGCAGTGGAGCCT[C/G]AGTGTTCAAAGTGGA | 7874 |
rs527523349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8933242 | CGCACCCAGCTCCCA[A/G]TAGAATGTTAAAAAA | 7874 |
rs527533678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8901743 | GTACAGACAGAAAGG[C/T]CTGAAACGCCTGAGA | 7874 |
rs527625207 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8911922 | GTTCCCACCAGCCAC[C/T]GTGGAAAAACCGCTG | 7874 |
rs527638519 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8930187 | CTGAAAACTAGCTAC[C/G]CTCAGAAGTACCCAA | 7874 |
rs527723961 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8934282 | ACAACTGCTCTGTAA[C/T]TCTGAGGTACAGGTT | 7874 |
rs527734475 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957558 | ACACCAGCCTGAACA[C/T]AGCAAGACCCCATCT | 7874 |
rs527737610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8952992 | CAGTCGCGTGTCACC[A/G]TGCCAGGCTATTTTT | 7874 |
rs527766847 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8897218 | CAGCTGGCCCCCATG[G/T]TCTTGCTCTCATTCC | 7874 |
rs527801292 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8930495 | TGTTGCCTAATCATT[A/C]ATAAATTCCAATTGT | 7874 |
rs527827280 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957140 | ACCAACCCTCAGAAG[G/T]AGACCTGCTTCTCTT | 7874 |
rs527830010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8896836 | CACTGGGTCTGTGTT[A/G]AGCTTCTGTGCAACT | 7874 |
rs527838265 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8917952 | ACGCCGCCATGCCCA[C/G]ATAATTTTTTTGTAT | 7874 |
rs527869158 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8921367 | TTTTAAAGACAGTAA[A/C]CATAGCACACCAAAA | 7874 |
rs527912091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8920931 | GGAAATTTAGCCCAC[C/T]GGGAACTCCCTTTGA | 7874 |
rs527985111 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8948787 | GAAAACACAGCGAAA[C/T]CCCGTCTCTAGAAAA | 7874 |
rs528133100 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8954790 | ATGGTAAAACCCCCC[C/G]TCTACTAAAGATACA | 7874 |
rs528187498 | in-del | -/A | 0.164781 | 0.235027 | intron-variant | USP7 | GRCh38.p7 | 16:8901324 | AACAAAAAAACGAAA[-/A]AAAAAAAACAGTAAG | 7874 |
rs528212211 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8932234 | AGATCAATTTCAGTC[C/T]TGATAGTCTCTTAAT | 7874 |
rs528213918 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8927461 | CTAATACAACTTCTT[C/G]CAAGTCCTAGTCAAT | 7874 |
rs528305508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8922611 | AGGTGCAGTCCAAGT[C/T]AGCAGCTTCCCCTGG | 7874 |
rs528308561 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8955294 | TCTCACCCCAGGCTA[C/G]AGTGCAGTGATGCAA | 7874 |
rs528325538 | in-del | -/GCC | 0.00557542 | 0.0525036 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964032 | GGGAGCGACCCGCCT[-/GCC]GCCGCCGCCGCCGAG | 7874 |
rs528334809 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8914157 | TATAAAGGAAGACAT[C/T]CAAATTGCCAATAAG | 7874 |
rs528343593 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961343 | AACAAAAATACAAAA[A/G]TAGCCAGGCGTGGTT | 7874 |
rs528380566 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964454 | AGAATTTATTTTCTC[A/G]CTGTCAGCCTAATCT | 7874 |
rs528388432 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8918706 | CCCAGCTACTCAGGA[A/G]GCTGAGGCCAGAGAA | 7874 |
rs528394922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8951521 | CTCTGCAGGCTTGGA[A/G]AGAGCCCCTGGATAT | 7874 |
rs528432577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950655 | TCTGCCACGAACATG[A/G]CACTGCTAATTGTCC | 7874 |
rs528445981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8914785 | TTAGCTGGGTGTGGT[A/G]GCACACGCCTGTGTT | 7874 |
rs528460288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8941738 | TGTGTTGGGTGGTGC[A/G]TGCTGTGAAGTCAGG | 7874 |
rs528506388 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8946309 | AAAATGGCAGGCGGC[A/G]GTGGCTTAAGCCGGT | 7874 |
rs528513390 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8940572 | CTGCATCAGAAAGGG[-/A]GAGGTGGGAGCCTGT | 7874 |
rs528531231 | in-del | -/TGCTAA | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8920579 | ACATCCCAACTTTTT[-/TGCTAA]TTTTAGACTGTTTCA | 7874 |
rs528550525 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957098 | TACTAATTACTGTTT[C/T]CAACTTCCAAATAAA | 7874 |
rs528614144 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8928481 | TAGCCCAGCACATAT[C/G]CAACTTCCTAGAATC | 7874 |
rs528670427 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8940367 | TGAGCTCCAGCACAG[C/G]ACCAGCCTCCAGCAC | 7874 |
rs528675644 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960872 | TTAAACCACACACCA[C/G]TGGGTACTCACAGGG | 7874 |
rs528695418 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8916171 | GAAGTCACCACTGTA[C/T]AGTGACTCAGGACCA | 7874 |
rs528700914 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8932928 | AAGGCCTATTAAATA[A/T]ATTATGGCACATTCC | 7874 |
rs528726913 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937406 | AATTAGCCAGACGTG[A/G]TGGCGCATGCCTGTA | 7874 |
rs528757443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8895875 | ACAGTCTCAATCTGT[C/T]GCCCAGGCTGGAGTG | 7874 |
rs528778354 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8917783 | TATTGGAGCACCATT[G/T]CTTTTTTTGTTTTGT | 7874 |
rs528839159 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961275 | AGGCGGGCAGATCAC[C/G]TGAGGTCGGGAGTTC | 7874 |
rs528851854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8943857 | TCGTGCACTGATGCA[C/T]AACTTTAAACATAAG | 7874 |
rs528856578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8916906 | GATTAAATGCTCAAG[C/T]CTCCCTAAATTAAGT | 7874 |
rs528863299 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8915607 | AATTGACTAGAAATA[A/T]CAATGTTCAAAGAAG | 7874 |
rs528889913 | snp | A/C/T | 6.83515e-05 | 0.0058456 | intron-variant | USP7 | GRCh38.p7 | 16:8921313 | GTTTAAAAGAATAAT[A/C/T]TGAGCCTTAGTTGAC | 7874 |
rs528892144 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | USP7 | GRCh38.p7 | 16:8916657 | TGGATAATCAGCTAT[C/T]ATTCTCAAATTCCTT | 7874 |
rs528963071 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8939218 | CTGAACAGTTCCAAC[A/T]CCACAAGGATCCCTC | 7874 |
rs528992524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8912385 | AACCCAGGAGACAAA[A/G]GTTGTAGTGAGCTGA | 7874 |
rs529010690 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8930645 | TTGCTTTATTTGCAA[G/T]GATATTCTGCACAAA | 7874 |
rs529051989 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8907612 | AGTAATCCCAGCACT[A/T]TGGGAGGCTGAGGCC | 7874 |
rs529085196 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8902905 | AAAAGACTGTGATTC[C/T]AAGAAAAAGAATTCT | 7874 |
rs529096424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8934714 | CTGCCCTTTTCCACC[C/T]GACAGGTGCAGAGAA | 7874 |
rs529167689 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8930838 | GCTGGGTGTGGTGGC[A/G]CATGCCCGCAATCCC | 7874 |
rs529167913 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8898049 | TCCCTGAGATCAGGC[C/G]GCGGCAGGAAGAGCT | 7874 |
rs529178246 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8895285 | GCCACACCTGGATCC[A/C]GCCAGAGTGATGGGC | 7874 |
rs529245312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8926750 | CCAATCTGCCTGGAT[A/G]CCACTAACATTAGCA | 7874 |
rs529249614 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964081 | GCCGCGCCCCGGCAC[C/T]GCCTGCGCCGCAGCC | 7874 |
rs529274616 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893733 | CCTCTTCTCCCCCAT[C/T]GCGCTGACAGTTGCC | 7874 |
rs529312260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8958642 | AAAGCCGACTCCCAA[C/T]GTCTGGACACTCAGG | 7874 |
rs529386876 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8944743 | GGGGACCTACTCAGA[C/G]TCTCATGGAACACCT | 7874 |
rs529409351 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8922263 | GCAGGCCGAGACAGG[C/G]AGATCACCTGAGGTC | 7874 |
rs529410202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8917463 | AGCTCACTACAACCT[C/T]CGCCTCCTGGGTTCA | 7874 |
rs529450424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894244 | ACCTGAGCTACACGC[C/T]CACCTGGAGCTAAGG | 7874 |
rs529453812 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8944995 | AGTGGCTCACGCCTG[C/T]AATCCCAGCACTTTG | 7874 |
rs529460341 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8955152 | GTTCTAAGAATAACC[A/G]CTGAAATGTAATTTT | 7874 |
rs529497980 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8936217 | AACAACCTAGTGATC[A/G]AAACTACAGCTGTTA | 7874 |
rs529508069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8913310 | GCAGTGAGCCGAGAT[C/T]GCACCACTGCACTCC | 7874 |
rs529514546 | snp | A/G | | | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8903331 | CAATACTTTGAACAC[A/G]GTGTATTTCACTTTT | 7874 |
rs529515533 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964706 | CTGAGGCTGGAGGTT[C/T]GCTTGGGAGGTTGAC | 7874 |
rs529535926 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8904092 | ACTCCTGAACTGGCT[C/G]TGCCCGCCACCAACA | 7874 |
rs529541152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8913325 | CGCACCACTGCACTC[C/T]AGCCTGGGCAACAGA | 7874 |
rs529565592 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8909300 | TCTGGCTGGAAATCC[A/T]CCTGCCCAGCAGCCA | 7874 |
rs529572216 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8908728 | AGCAATCAGGGAAGA[A/T]ATGGTTAAGGAAATT | 7874 |
rs529579475 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8911226 | GACAAGGAAAACCTC[A/G]ATTTCCTCAGAGGTC | 7874 |
rs529631948 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8943555 | GAAACACAAACGACT[A/C]ACCAACAGGCTCCAC | 7874 |
rs529665018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8955767 | ATGAAATATAATTTA[C/T]TCCCCAAAGTCTTAT | 7874 |
rs529689855 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8965075 | CAGGGGAGAATAGAA[A/T]TTCACCCTAACAAGG | 7874 |
rs529737595 | snp | C/T | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8952122 | TGGCCAGGTGTGGTG[C/T]GCCTGTAGTCCCAGT | 7874 |
rs529749053 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8946424 | CATCTCTAAATAAAG[A/T]AAAAAACTGTTGATC | 7874 |
rs529771782 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8951612 | GCGCATGAGGCTATA[C/T]TTAGGTCTAAAATGC | 7874 |
rs529772853 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8924484 | GCCTGGAAGGCTGTT[C/G/T]CCGGCTTAGAATCAG | 7874 |
rs529773648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8956105 | AGCTGGAGGTTAGTA[C/T]ATAACACAGGACACT | 7874 |
rs529780037 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8945081 | AGATGATGAAACCCC[A/G]TCTGTACTAAATAAA | 7874 |
rs529858297 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8927216 | AGTCCCAGCTGCCTG[C/G]GAGGCTGAGGCAGGA | 7874 |
rs529869039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8942346 | GTACCAGCCCTTGCC[A/G]AATATCAAGCAGTGG | 7874 |
rs529902649 | in-del | -/AAAAT | 0.00398564 | 0.0444627 | intron-variant | USP7 | GRCh38.p7 | 16:8904973 | AGACTCCGTCTCAAA[-/AAAAT]AAAATAAAATAATCT | 7874 |
rs529908008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8946678 | CACCTCCAATAATCT[A/G]GTCACTGGCCTATAC | 7874 |
rs529939499 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8942885 | AGTTATTTGGCCATA[G/T]GCACCCTCATTAGGC | 7874 |
rs529943689 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | USP7 | GRCh38.p7 | 16:8929750 | ACTGATTTCCTACAC[-/A]AAAAAATGTCCATGC | 7874 |
rs529952287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8914947 | CAAACAAATACATCC[C/T]ACTACAAGGTTCTAT | 7874 |
rs529974365 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8905748 | ATGAGCTGTTTTATC[A/C]TATCCCATGGCATTT | 7874 |
rs529997099 | in-del | -/ACCC | | | intron-variant | USP7 | GRCh38.p7 | 16:8930043 | CAGGCAGGAGTAAAT[-/ACCC]ACCTATTAAATTTAA | 7874 |
rs529998301 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937550 | CTGTCTCAAAAAATA[A/G]TAAGTTGGGTGTGGT | 7874 |
rs530026016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8906114 | CCAGCCAGCCTCCCC[A/G]ACTGGGCCCACCGCA | 7874 |
rs530035505 | in-del | -/TGTC | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8918360 | ATTAGATTTAATGTA[-/TGTC]TATTCTTTTTGTTAA | 7874 |
rs530046012 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8903909 | AAGAAAAGGAGACTG[G/T]GTTTCACTGCAATAA | 7874 |
rs530076294 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8940743 | ATCAATCCCCTCTGC[A/G]AGGCCTCTCCTAGGT | 7874 |
rs530085035 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8933914 | CCGTGTGCCACCACG[A/C]CCAGCTAATTTTTTT | 7874 |
rs530093136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8902295 | TTCTAGTTAAGTGGA[C/T]CAAAAGGGAAACAAG | 7874 |
rs530095964 | snp | A/C/G | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8953899 | GAAGACACGTGCCCC[A/C/G]TGCGGCGCCACTGGA | 7874 |
rs530100361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962351 | GCCTTCCAACGACCA[A/G]CTCCCTAAATCCAAC | 7874 |
rs530100631 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8896465 | CCAAAAGCCATTTGT[C/T]CTCCAAGCGACTACA | 7874 |
rs530163568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8895962 | CCACCTCAGCCTCCC[A/G]AGTAGTTGGGACTAC | 7874 |
rs530171549 | snp | A/C | 0.00835141 | 0.0640778 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956771 | TCGTATTAAAAAAAC[A/C]AAAACAAAAAAAAAA | 7874 |
rs530179441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8901677 | TTGTCGATAAAGTTG[C/T]ACTGGAAGACAGCCA | 7874 |
rs530191108 | snp | C/T | 6.61376e-05 | 0.00575017 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8920402 | CAAAGACTTCAAAGG[C/T]AACTTTGTCATCATC | 7874 |
rs530192274 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP7 | GRCh38.p7 | 16:8929306 | CACACCATTGCCCTC[A/G]TCTACGGTGGAAAGC | 7874 |
rs530194401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8925533 | CTTTCACCCTATACA[C/T]TAAATTTTCCAAGGT | 7874 |
rs530261743 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961986 | CTTTGTCATTTGCAA[A/C]CTGGCCAGCCATTTT | 7874 |
rs530274969 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8930110 | GACTCTACTTACCTG[C/G]CAATGGTGTAGGCAA | 7874 |
rs530282381 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8952230 | ATTCCAGCCTGGGCA[C/T]GAGGGAGAGCCTGTC | 7874 |
rs530312840 | in-del | -/CACCTCCCACGTTA | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8943567 | CTAACCAACAGGCTC[-/CACCTCCCACGTTA]CACCTCCCTCGTTAA | 7874 |
rs530319526 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892290 | GGGAAGGGCCAGGTC[C/T]GCGGGGACCCTCACT | 7874 |
rs530337604 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8952763 | AAACCACAGACCCTA[A/C]ACCTCTAGTCACAGA | 7874 |
rs530363889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8925063 | AAGTTTTGCCATGTG[C/T]TTTTAGGATCATGCA | 7874 |
rs530368668 | snp | C/G | 0.00557542 | 0.0525036 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892657 | CCTGCCCCCGCAAAA[C/G]GGAATTAGAAGGAAA | 7874 |
rs530407662 | snp | A/T | 6.66245e-05 | 0.00577129 | intron-variant | USP7 | GRCh38.p7 | 16:8903410 | GCGACTATCTGAAAA[A/T]ATGTATGAAAGCACA | 7874 |
rs530412191 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8947935 | CATTATGCCTGGGGA[C/T]TTCTCTGTCTCCAGG | 7874 |
rs530482385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8958741 | CGCAAGAATCATCAG[A/G]AGGCCACCAGGCTGA | 7874 |
rs530489899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8935634 | GTCTATAGGAAATAA[A/G]GCAATTACCATCCCA | 7874 |
rs530490664 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8898694 | TTTGCCTAAAAACAA[A/G]TATCTGTGAGTGAGC | 7874 |
rs530505721 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8931253 | GAGTGCAGTGGCGCA[A/G]TCTCAGCTCACTGCT | 7874 |
rs530521220 | in-del | -/AAGT | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8962025 | CTATCCAATTACTGG[-/AAGT]AAGTTATTCTATTCA | 7874 |
rs530522935 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8940282 | CCTCTGCAAGTAGCT[A/T]ACCATGCTTTGTCCA | 7874 |
rs530563909 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8903875 | TCTGTCTCAAAAAAA[A/C]AAAAAAAGGAAAAGA | 7874 |
rs530575692 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964692 | AGCTACTTGGGAGGC[C/T]GAGGCTGGAGGTTCG | 7874 |
rs530576128 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8922374 | ACGCCTATAGTCCCA[C/G]CTACTTGAGACGCCG | 7874 |
rs530623213 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894326 | CTCAATCACCCTGCA[C/T]ACATATCCAAGCTTC | 7874 |
rs530627290 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8949277 | TAAAATTAAGGTTAA[C/G]TGGCATTTAACATCG | 7874 |
rs530645089 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961893 | AACCCAGTCCTTGGC[A/G]TGGACTCCGCTCTTC | 7874 |
rs530693260 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8927342 | AAAAAGAAAGAAAGT[G/T]AAAGAAAAACAGAAT | 7874 |
rs530737507 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8922544 | CACTCTGGGGAACAT[A/G]TTACTGAGGGTTCCA | 7874 |
rs530781265 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8931867 | AACTAATGCTGGCCC[C/G]ACGGTTGCCTACACA | 7874 |
rs530809256 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8918670 | AAAAATTAGCTGGCC[A/G]TGGTGGCGGGTGCCT | 7874 |
rs530812652 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8946290 | AAAACACAACAACAA[A/C]AAAAAAATGGCAGGC | 7874 |
rs530828355 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8945354 | ATGCCACTGTACTCC[A/T]GCTTGGGCAACACAG | 7874 |
rs530845104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8918235 | CAAACATGCCTTGAA[A/G]GATGACAAGCCAGCC | 7874 |
rs530879035 | snp | A/C/G | 0.00499608 | 0.0497654 | intron-variant, synonymous-codon | USP7 | GRCh38.p7 | 16:8894530 | CCCACACCAGCCCCC[A/C/G]GGGGGGGGAGAACCC | 7874 |
rs530889273 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8940618 | CCACAGAAACAGGGA[A/C/T]GATGGTGGCAGCCAA | 7874 |
rs530889785 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957362 | TACATGGCAAGAAAT[A/T]TGTTGTTACAACTCT | 7874 |
rs530905983 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8932841 | AAGATGAAAAATTTT[C/T]AAGAAGTAACATGTA | 7874 |
rs530946144 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950504 | TCTCCAGACCCCTTA[A/C]CCCAAGGCAATTAAC | 7874 |
rs531040071 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8914031 | GCATGAGCGACCACA[A/C]CCATCCTCCCCCTTA | 7874 |
rs531092715 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8932787 | GGGAATGGGGCTGGG[A/G]ATGGACAAAGCAGGA | 7874 |
rs531109913 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8904862 | CTGTAGTCCCAGCTA[C/G]TTGGGAGGCTGAGGC | 7874 |
rs531154251 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8955270 | TGATGGACAGTATTG[C/G/T]GGCCAGTGTCTCACC | 7874 |
rs531158707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960171 | AGCAACCTTATTCCC[A/G]GCCAGACCTAATCAT | 7874 |
rs531196126 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960781 | CGGGTCCTAAGTCAC[A/G]TTCCAATCGTAAGGC | 7874 |
rs531197835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8900422 | ACATTAAAAAAAACA[A/G]AAACAAAAACGTGGC | 7874 |
rs531203594 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8920770 | ACTTAGCATAGTAAG[A/T]AGTAACATTCCTAAG | 7874 |
rs531249453 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8930638 | CTATAATTTGCTTTA[A/T]TTGCAATGATATTCT | 7874 |
rs531261876 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8900034 | AGCACCTGCTCTCCT[A/C]TACAGGAGCAGACCC | 7874 |
rs531276418 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8905098 | ATAAGCATAAAATGT[A/G]TTTGGACAGAAAAGG | 7874 |
rs531286139 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8932092 | CTCCAAAACCCCAAC[C/G]CTTAGATTACATCAT | 7874 |
rs531293216 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8949689 | GCTCACCTCTGTGCA[C/T]TCATCACCTTCTGCC | 7874 |
rs531296154 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8943495 | ATCTGTGACACACAA[C/G]AGCCAAAGGATCAAC | 7874 |
rs531302270 | snp | C/G | | | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962244 | CCTCCATTTGACTCC[C/G]GACAGCCTGAACTCG | 7874 |
rs531311025 | snp | C/G/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937233 | AAAAAAGGATTAACA[C/G/T]GAAACAACGTGTATA | 7874 |
rs531315775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8916612 | TTTCAAATGAGCAAA[C/T]TAAAAGTAACTTAGA | 7874 |
rs531334262 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8943045 | GTGTTCAAAGTGGAC[A/C]CACTTTGACGCTTTG | 7874 |
rs531335934 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8947839 | CTAGGTGGGCATGCC[A/T]TGCCCCTCCCTGCAC | 7874 |
rs531368084 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8939164 | ACAATTTTATTTACT[A/G]TGTAGATTTGTGTGT | 7874 |
rs531373348 | snp | A/G | 3.32436e-05 | 0.00407685 | intron-variant | USP7 | GRCh38.p7 | 16:8908308 | GACCAGCATGATGAT[A/G]AAATCTTAACTTTAT | 7874 |
rs531410412 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8910930 | TTAGGATTAGCAGAG[A/G]AGGTAAACAACACTA | 7874 |
rs531492918 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8934626 | GCAAGCAGAGGTCTG[C/T]GGTTGCAGCAGAATC | 7874 |
rs531506337 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8934328 | GCAGTGAAATCAGAC[G/T]GAGACACAAGTGAAT | 7874 |
rs531514908 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8906693 | TTTAATAGGATAAGC[A/G]TGAATTGCCTTGGGA | 7874 |
rs531572825 | in-del | -/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8932951 | CACATTCCAATGGAA[-/T]TTTTTTTTTTTATGG | 7874 |
rs531603086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8896894 | GAGTCTGGGAATGAC[A/G]CGCATGGATCCCAGC | 7874 |
rs531616722 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8897242 | TCATTCCCACCCCAA[A/C]TCCCTCATCTGTGAA | 7874 |
rs531620378 | snp | A/G | 0.000117013 | 0.00764805 | intron-variant | USP7 | GRCh38.p7 | 16:8930259 | TTCTGACAAGTTTCC[A/G]CCCACTGCGAGGCGG | 7874 |
rs531636503 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962494 | TCGAGTCAGGTTTGA[G/T]TCTGATGCAGGCAGC | 7874 |
rs531649013 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8953789 | CGTGCCCCCTGCGGC[G/T]CCACTGGAGGCAGAG | 7874 |
rs531656065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8930627 | GCTATACCACACTAT[A/G]ATTTGCTTTATTTGC | 7874 |
rs531680107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8907110 | GGCCTGCGAAGCAGC[C/T]ACCACTCAGCTCACA | 7874 |
rs531703255 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8926574 | CAGATTGTCCTCCTA[C/T]GAGGAATTACATGAG | 7874 |
rs531746151 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8901873 | AACAGGACGGCCCCA[C/T]GTGGCTGCTACTGTC | 7874 |
rs531755844 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893206 | AAAAGGCTTTCTTGT[C/G]GTCTGTTCCACTTTA | 7874 |
rs531854173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8907875 | AACTGGCATACAAAC[A/G]ACTACTTTAGCATTC | 7874 |
rs531939339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8944597 | CCTTTATTTGAATAA[A/G]ACCACAAAAGGGAAC | 7874 |
rs532003391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8913247 | TCTAATCCCAGCTAC[C/T]TGTGAGCCTAAGGCA | 7874 |
rs532024302 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8944937 | ATATGGCGAAACCTC[A/G]CCTCTACTAAAAATA | 7874 |
rs532094900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8895318 | TCATGGGAGTCTCAG[C/T]CAGAAGATATCCAAG | 7874 |
rs532095792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8928045 | ATAGTGAATAAGGAA[C/T]TAAAAGTAGAATGAG | 7874 |
rs532123053 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893030 | ATCAACATCAGTGAA[A/G]TTCACTTGCAGACTC | 7874 |
rs532142683 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8900000 | CATCCCACTACAAAA[C/G]AAAACCCCCTTAGGT | 7874 |
rs532151493 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950369 | AAAACAGTATTTTAA[C/G]AAAAATAAAAGCCCT | 7874 |
rs532176659 | snp | C/G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8931966 | TTTTTAACAGCCAGG[C/G/T]AGTTGTGTGTGTGGC | 7874 |
rs532183216 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8932302 | CCGACCCGTGGCTCA[A/C]TGCCTATAATCCTAG | 7874 |
rs532234669 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8918737 | TCACTTGAACCCAGG[A/C]GACAGAGGCTGCAGT | 7874 |
rs532241059 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8910592 | CATCCCCCTCTCCCT[A/C]CCCATTCAATTATCC | 7874 |
rs532265645 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8945791 | GTGGTGGCTCATACC[C/G]TATAATCCCAGCACT | 7874 |
rs532281274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8894924 | ACGTCACGTGGCAGC[C/T]GCCAAAACCAACGCC | 7874 |
rs532292995 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8946622 | AAAAGTCAGAATAGC[C/T]GAACTGACACTCTGA | 7874 |
rs532324556 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8919073 | CGTCTGTAGCAGGCT[A/G]TTCATGTAACAAGTC | 7874 |
rs532351333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8911069 | TATGGAGGTAACAGT[C/T]AAGGTTTTACTGTTA | 7874 |
rs532374033 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8923787 | TGTTCAAGGACGGGA[C/T]TTCTGGGGGTAAAGA | 7874 |
rs532394297 | in-del | -/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937984 | ACTCCAATGAGCCCC[-/T]TATTATGTGCCAGGC | 7874 |
rs532426990 | in-del | -/TCCAGAACCTGGAATATATACAGTC | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8940873 | CACTTATATACAGTG[-/TCCAGAACCTGGAATATATACAGTC]TCCAGAACCTGGAGG | 7874 |
rs532441845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8914881 | CTATGGTTGCACCCC[A/G]GCCTGTACAGCACAA | 7874 |
rs532462480 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8946341 | ATCCCAGCACTTTGA[C/G]AGGCTGAGGCAGGAG | 7874 |
rs532513598 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937470 | TCACTTGAACCCAGG[A/T]GGCGGAGGTTGCAGT | 7874 |
rs532529171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8924696 | CAGCCACTTCTCAGG[A/G]AAGAGAATTTGCTTG | 7874 |
rs532553821 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8942265 | AGGTACTGGGACACT[C/T]GGAGTGACTGGGATG | 7874 |
rs532560337 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8929284 | CAACAACCAGCGAGA[A/C]CACACCCACACCATT | 7874 |
rs532614346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961319 | CCAACATGGAGAAAC[C/T]CCGTCTCTAACAAAA | 7874 |
rs532625901 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8933524 | TCTACAGAAACAGCA[C/G]GATACAGAAGAACCT | 7874 |
rs532689844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8925029 | TAAGATAATAACGTC[C/T]AGAATGGCGTGGTGG | 7874 |
rs532729216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8956189 | AAAGAGGGGCCTGGA[C/T]TTTTTAATCTTCTAT | 7874 |
rs532743125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8912795 | AAATACATAGAAAAA[A/G]AAGAAGAGATAAAGA | 7874 |
rs532744799 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8907289 | CAAAGAAACATACCA[A/G]CAGGTTGGAATTGGT | 7874 |
rs532749129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8895956 | ATTCTCCCACCTCAG[C/T]CTCCCGAGTAGTTGG | 7874 |
rs532837749 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8892246 | CTCTCGCACCCCTGC[C/T]CTAACTCCTCTTTCT | 7874 |
rs532849818 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8939676 | CTCAATGTAATGTTC[A/G]TATGTACATATCATG | 7874 |
rs532862708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8935344 | CCTCCTGAGTAGCTG[A/G]GATTACAGGCACCTG | 7874 |
rs532893470 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956742 | CACTCCAGCCTGGGT[A/G]ACGAATTAAGACTTC | 7874 |
rs532903280 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891952 | GGGTTACAGTGAGGC[C/T]GGAGAAGGGGAGTTC | 7874 |
rs532903744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8907695 | AAAAATACAAAAATT[A/G]GCCAGGTACTTGGAA | 7874 |
rs532915148 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8926407 | TCGCTTGAACCTGGG[A/T]GGTGGAGGTTGCACT | 7874 |
rs532922786 | snp | C/T | | | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891628 | GCCTCCATCAGGAAG[C/T]GATGGTGTCTAGACG | 7874 |
rs532931226 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8939859 | AATCACAGCACTTTG[A/G]GAGGCCAAGGAGGGC | 7874 |
rs532942486 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8913237 | GGCGCATGCCTCTAA[C/T]CCCAGCTACTTGTGA | 7874 |
rs532954868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8939264 | GACCACCCACCCCGG[C/T]GTGCGTGCTCCCCCA | 7874 |
rs532991244 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8897730 | AAAAAAAAAAAAATA[A/T]ATATATATATATATA | 7874 |
rs532991484 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8898079 | TGGAGAAGGATCCTC[C/G]TCCTCAGCCAAGTGG | 7874 |
rs532994706 | in-del | -/G | 0.00250391 | 0.0353109 | intron-variant, frameshift-variant | USP7 | GRCh38.p7 | 16:8894530 | CCACACCAGCCCCCG[-/G]GGGGGGGGAGAACCC | 7874 |
rs533027518 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964102 | CGCCGCAGCCCCGCG[A/G]CGGACCCTCGGCGCT | 7874 |
rs533073508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8926788 | ATTTCATTACCGCAT[A/G]CTTCTTTTTACTGTA | 7874 |
rs533098762 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8931204 | TCTTTTTTTTTTTTT[C/T]CTGAGACAGAGTCTC | 7874 |
rs533113298 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8911042 | TCTTTCTTAAGGACA[C/T]TAAAATGACAATATG | 7874 |
rs533116495 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8928843 | GAAGGGGACTTTACC[A/C]ATATTGTCCCCTCAT | 7874 |
rs533120313 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP7 | GRCh38.p7 | 16:8918426 | TCAACTCAGTTTTTA[C/T]ATAAAACTTTGCAAA | 7874 |
rs533141361 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8958442 | TTTCAGCAAGGCAGT[A/G]ACGGACAGAAGTCCT | 7874 |
rs533166310 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8903745 | GGTGGCACATGCCTG[C/T]AATCCCAGCTACTAG | 7874 |
rs533186734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8949385 | CTACTGTTCGAGGCA[C/T]TGAAAATGCCTGGGG | 7874 |
rs533191868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8935577 | TTGGCAAACACAAGT[A/G]ACTATGTGCAATGTC | 7874 |
rs533198860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8922315 | CCAACATGGTGAAAC[C/T]CCGTCCCTATGAAAA | 7874 |
rs533276283 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8945032 | CAAGGCAGATGAAAG[A/T]CCTGAGGTCAGGAGT | 7874 |
rs533311961 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893824 | CATTTTGCTCAAAAA[A/G]GGCAGTCAATAGATA | 7874 |
rs533338744 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP7 | GRCh38.p7 | 16:8936058 | AAGCTGGCAGGGGGC[A/G]GGGGTCGCGAACACA | 7874 |
rs533378876 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8954736 | AATCCCAGCACTTTG[C/G]GGGTCTGAGGTGGGT | 7874 |
rs533433563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8913577 | GTTAAAATGTCTTTC[A/G]CAACTGCAGATGAAA | 7874 |
rs533459164 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8965448 | TACTCAGGAGGCCGA[A/G]GCAGGAGAATCACTT | 7874 |
rs533470800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8913330 | CACTGCACTCCAGCC[C/T]GGGCAACAGAGCGAG | 7874 |
rs533471748 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8933305 | AATCCCAGCACTTGT[C/G]GGGGGCCAAGACGGG | 7874 |
rs533512521 | snp | A/C | 0.046775 | 0.145601 | intron-variant | USP7 | GRCh38.p7 | 16:8904696 | GCCTGTAATCCCAGC[A/C]CTTTGGGAGGCTGAG | 7874 |
rs533545099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8909357 | CATGACAAGGCACAC[C/T]CATATGCCAAGGTTC | 7874 |
rs533565716 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8946483 | AGAAAGAAGCTGTTA[A/T]GTGAATACACACGAG | 7874 |
rs533606270 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8953512 | GACACGTGCCCCATG[A/C]GGTGCCACTGGAAGC | 7874 |
rs533640319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8942362 | AATATCAAGCAGTGG[A/G]GTCTGTCCCACCCTT | 7874 |
rs533645854 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8954833 | GGTGCGGTGAGGGGC[A/G]CCTGTAGTCCCAGCT | 7874 |
rs533651660 | snp | A/G | 0.00026617 | 0.0115332 | intron-variant | USP7 | GRCh38.p7 | 16:8936556 | CCATCACCAGCATAA[A/G]GAGCTCAACCTGAAA | 7874 |
rs533712725 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8933630 | CTATCATTTTTTTTT[C/T]CTCAAAGAGACAAGA | 7874 |
rs533726486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8905806 | AAGTCAACGTAGCAT[A/G]TTCCTAACAGTTATC | 7874 |
rs533758026 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8915011 | CAGGGTGTTAGAAGT[C/G]CACGTGGTGGTTTCC | 7874 |
rs533835503 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8911239 | TCGATTTCCTCAGAG[G/T]TCAACACGGGGTGGG | 7874 |
rs533841312 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961451 | GACCCGAGATCGCGC[C/G]ACTGCACTCCAGCCT | 7874 |
rs533848837 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8952259 | TCTCCAAAAAAATAT[G/T]AATTAAAATTCAGTA | 7874 |
rs533849455 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8905486 | GGCACACAATCTGAC[A/G]GTGTGCTAGGCAGGC | 7874 |
rs533875735 | snp | A/T | 1.65831e-05 | 0.00287945 | intron-variant | USP7 | GRCh38.p7 | 16:8910834 | ATTCAAATACTTTAA[A/T]GAGAGAGAGAGAAAA | 7874 |
rs533882836 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8901312 | AAAAAACAAACAAAC[A/G]AAAAAACGAAAAAAA | 7874 |
rs533885757 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937320 | GAGGCTGAGGCGGGC[A/G]GATCACCTGAGGCCA | 7874 |
rs533901383 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8913517 | GACGGTAGAACGTCT[A/G]ACAGACCGAAGGAAG | 7874 |
rs533920718 | snp | A/C | 0.0119351 | 0.0763224 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956781 | AAAACAAAAACAAAA[A/C]AAAAAAAACACTGAA | 7874 |
rs533941830 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, nc-transcript-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8892066 | GTGGAAAAGGGAACG[C/T]GGCAGATGACGGAAA | 7874 |
rs533943814 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8896583 | GGAACAGAAGTGACT[C/G]AATCTGTCAAATACA | 7874 |
rs533967730 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8900814 | ATCAGATTTGATTCT[A/G]CAACAGGTAAAAAAA | 7874 |
rs533975968 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8960060 | CGTCTACACCGACCA[C/T]CTGAGTATTCAGAGG | 7874 |
rs533977417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8933136 | GTAGAGACAGGGTTT[C/T]ATCATGTTGGTCAGA | 7874 |
rs534048009 | snp | A/T | 0.000258467 | 0.0113652 | intron-variant | USP7 | GRCh38.p7 | 16:8920468 | AAACATAAATAAGAA[A/T]ATCCAGCTTGAATAA | 7874 |
rs534119362 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8911772 | GATCTGGGGATGTGC[A/C]GTTTCTTCCGAAGCT | 7874 |
rs534133326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8925166 | AGGAAATGGAGGTTC[A/G]CCGAGGCTGTTTTAC | 7874 |
rs534173494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8952528 | CCTAGAGCCACCCCA[C/T]TCCTGGGCTCCCCCT | 7874 |
rs534189331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8906837 | ATGATTCTGAAGGTC[A/G]AGGTTAAGACTACTA | 7874 |
rs534226293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8929359 | GCGGGTTTAGACCAC[A/G]CCTCTTTACCTTCCT | 7874 |
rs534238589 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8947386 | AGGGTCTCACTCTTA[C/T]CACCCAGGCCGAAGT | 7874 |
rs534278500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8922050 | CACTACTTTTCCAAA[A/G]TGCTTCAGGCTAAAG | 7874 |
rs534307454 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8898733 | AAACCGCTGGCCTTA[A/C]ACCTGGTCTTGAAAT | 7874 |
rs534438785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894347 | TCCAAGCTTCTCTCC[C/T]TGAAGATCTCACAGG | 7874 |
rs534491315 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8930751 | AGGCGGACAGATCAC[C/G]TGAGGCCAGGAGTTC | 7874 |
rs534498058 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP7 | GRCh38.p7 | 16:8913412 | GAAGTGAAGCGAAGC[A/G]AAGAATATGGGGGCT | 7874 |
rs534498421 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8918298 | GATTTCCTGTACTGC[C/T]TCATAATAATCACAA | 7874 |
rs534534858 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938493 | CGAGGCAGGTGGATC[A/C]CAAGGTCAGGAGATC | 7874 |
rs534590107 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8918913 | ATGAACTAGCAGCCA[C/T]CTGAGGAGACAGGGC | 7874 |
rs534602080 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8935858 | CCGTGAATTCCATTT[C/G]TGATGTCATAACACA | 7874 |
rs534604994 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8913675 | CGAGAATCCATATCC[A/C]AATTAAAAACGGAGG | 7874 |
rs534615759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8909114 | TTCTCAACAAGCCTT[C/T]TATGGGGACACCGGA | 7874 |
rs534626904 | in-del | -/A/C/G/GC/GG/T | 0.00410054 | 0.0451333 | intron-variant, frameshift-variant | USP7 | GRCh38.p7 | 16:8894531 | CACACCAGCCCCCGG[-/A/C/G/GC/GG/T]GGGGGGGAGAACCCT | 7874 |
rs534628070 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956411 | ACACACGGGCATTTC[C/T]GCAACTATGAACAGC | 7874 |
rs534661664 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8933098 | GGTGTGTACCACCAC[A/G]CTTGGCTAATTTTGT | 7874 |
rs534664836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8932034 | CAAGCAATCTGATTC[A/G]GCACCACGGACAGTG | 7874 |
rs534703113 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8958727 | AGCTCTAGCACTCAC[A/G]CAAGAATCATCAGAA | 7874 |
rs534723113 | snp | A/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957683 | GGATCACCTGAGCCC[A/G/T]GAAGTTTAAGGCTGC | 7874 |
rs534763844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8954581 | AGCTGTAAGTTTATA[A/G]GATGTATTCTGGAAG | 7874 |
rs534769317 | snp | C/G/T | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8927622 | AGGTGGATCACCTGA[C/G/T]GTCAGGTGTTCAAGA | 7874 |
rs534773089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8932445 | GAAAACATATACACA[C/T]ACTTCTAAACTAGTC | 7874 |
rs534776158 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8955080 | ATTAATCACCTATAC[A/C]CACTTTCTATGAATC | 7874 |
rs534811143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8959549 | TTGGCCTAATTTCTC[C/T]CTACTGGGTTCTCTG | 7874 |
rs534836402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950049 | ACTGAGCGCTTGAAA[C/T]ATGGCTGTTGTGACA | 7874 |
rs534845735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8904920 | GAGCTTGCAGTGAGC[C/T]GAGATCGCGCCACTG | 7874 |
rs534857377 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8916927 | TAAATTAAGTGCCTA[C/T]AGTATGCTCTACTAA | 7874 |
rs534880579 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8909512 | TCTGTCTCCACCGCT[G/T]TCCACTGAGGCTTCG | 7874 |
rs534967229 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8951692 | GTGCACCTGCACCCT[C/G]AGCCCTCGCAGACAA | 7874 |
rs534977154 | snp | C/T | 0.0832709 | 0.186283 | intron-variant | USP7 | GRCh38.p7 | 16:8953794 | CCCCTGCGGCGCCAC[C/T]GGAGGCAGAGGGAAG | 7874 |
rs534993472 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8904672 | TATTAGGCCGGCGTG[A/G]TGGCTTACGCCTGTA | 7874 |
rs535021358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8923898 | CCTGGAAGCTCAGCA[C/T]TGCTCAGAGGCAAGA | 7874 |
rs535029062 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8925128 | TAGACAAGAGACAGA[A/T]GTCAATTCCCACATT | 7874 |
rs535048430 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8955844 | TAAGGGGCTGTGGAG[G/T]AGAAAGGTTTGCTCA | 7874 |
rs535066246 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8934782 | CACTGGTTGGCCACC[A/G]AGTACATAAGGGGTG | 7874 |
rs535088380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960267 | ACAGGGAGTGTGTGG[C/T]TGCAACCCCAGCAAA | 7874 |
rs535095791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8900092 | ACAGGTGGTGGAGCC[C/T]AGTCTCTGACCGTGA | 7874 |
rs535095848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8894728 | CCTAGGCCGCTACGC[C/T]AGGCAAGGCTTGAGC | 7874 |
rs535113595 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938426 | CACATCAAAAACACT[A/C]AGGGGGCCGGGCACG | 7874 |
rs535139692 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8911616 | AGCCCCGTGATGGGC[C/G]CAGCTCTGCTGAAAG | 7874 |
rs535157186 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8934369 | GCTCAAAGAAGGGCT[A/T]GTTTGGGTGACTTGA | 7874 |
rs535158717 | snp | A/G/T | 6.60943e-05 | 0.00574834 | intron-variant | USP7 | GRCh38.p7 | 16:8899588 | TCTGAAGAGGAAAGG[A/G/T]GCATTTATTAAATAC | 7874 |
rs535171829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8923577 | CCGAAGACTGAGATA[A/G]CATACAGTTTCTGAA | 7874 |
rs535173337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962512 | TGATGCAGGCAGCCA[C/T]GTGCGGCAGGGCTTT | 7874 |
rs535251962 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8925713 | TTCACAATTAGTGCA[A/C]TGCACACTCGATTTC | 7874 |
rs535276186 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957314 | CAAGTAATTTCTAAA[C/G]TAGGTGACATTTAAC | 7874 |
rs535321591 | snp | C/G | 0.00199481 | 0.0315187 | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891663 | TTCTCGCCCTGTCAA[C/G]GCACCCACGTTGCAG | 7874 |
rs535326715 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8953487 | AGTAAGAAACGGGGG[C/T]TGGGGAGAAGACACG | 7874 |
rs535334479 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957495 | ACACCTATAATCCCA[A/G]TGCTTTGAGAGGTTC | 7874 |
rs535339371 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8918840 | GGCGGTGGTAACTCT[C/G]AATCACTGAGGCAGG | 7874 |
rs535347573 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8914336 | CTGATGACTGTGCAA[C/T]TGATAAACCACTTTG | 7874 |
rs535371437 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8939276 | CGGCGTGCGTGCTCC[C/T]CCATTATCCCCGGCA | 7874 |
rs535390102 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8922206 | AAGAAAATGAAAGTA[C/T]GGCCAGGTGCGCTGG | 7874 |
rs535411938 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8892831 | AGCAAAAAGGCAATA[C/T]ACAGGAAGAGTTGGT | 7874 |
rs535470168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8905899 | TCTTCACTGTTCTCT[C/T]GTGCTGTCGGGTCCC | 7874 |
rs535481839 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8948615 | CATCTCTTTGCTAAA[C/T]CATGGTGAAGTTCCA | 7874 |
rs535504777 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956842 | GTAAGAGCCCAGCCC[C/T]CCCGCAGGCAGTGCC | 7874 |
rs535517066 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8902643 | GCCTGTAATCCCAGC[A/T]CTTTCGGAGGCCGAG | 7874 |
rs535545462 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962262 | CAGCCTGAACTCGTC[A/C]CGTAGGTAAGAAAAC | 7874 |
rs535555999 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8901950 | TCATCAGGAAGTCTA[C/G]TGAGCTTTTGTGGAA | 7874 |
rs535574967 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8939561 | ACACAAGCAAGCAAA[C/T]GTTAGCTAGCAACAA | 7874 |
rs535594919 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8956110 | GAGGTTAGTACATAA[C/T]ACAGGACACTGTCCT | 7874 |
rs535611101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8944105 | ATAATACATCAAGTA[C/T]ATAATGGTAGTTCCC | 7874 |
rs535644341 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8934576 | GTTCTAGTGTGAAGT[C/T]AGGGCTTCTCTGCAG | 7874 |
rs535648222 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8903134 | AGGAAATGTTCCTGG[A/G]TCACACTCCTCACTG | 7874 |
rs535683792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8925280 | TCCTGGAAGTTACCA[C/T]AACACACACAAAACA | 7874 |
rs535685886 | snp | G/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937328 | GGCGGGCGGATCACC[G/T]GAGGCCAGAAGTTTG | 7874 |
rs535782974 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8897785 | ACACCTGTAATCCTA[C/G]CTACTTGGGGGGCTG | 7874 |
rs535807459 | snp | A/T | | | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962401 | CTTCACATCCAACCT[A/T]TACAACCAAGACTCT | 7874 |
rs535839968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8917215 | AGGGGAATTTAAAAA[A/G]CAGTAAGAATTTAAT | 7874 |
rs535840230 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8912190 | GGCTCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 7874 |
rs535871560 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8921497 | CCCCAGTGTATTCTG[C/T]AGTGATTTCACTCAT | 7874 |
rs535878507 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8916811 | CCTTAAGCGGTGAAT[C/T]CTTTCTCAAGCAAAA | 7874 |
rs535886385 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8951839 | CACCTGATTCACAAA[A/G]GAAGCAATCTACCAA | 7874 |
rs535914398 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8923508 | GTTCTATACATCCTG[A/C]TTTAACTGCTAAAAC | 7874 |
rs535915843 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8943446 | GAGCTGCACAGATGC[A/G]GTTAGGGCAAGGGAT | 7874 |
rs535916472 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8912862 | AATAAAAAAAAATTT[A/T]AAAAGTTTGAAAATG | 7874 |
rs535955967 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8912499 | ATTACCAAGCATGCA[A/G]AGAAGCTGAAACCAC | 7874 |
rs536023137 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8935430 | TGGCCAGGCTGGTCT[C/G]GAACTCCTGACCTCA | 7874 |
rs536025119 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8910035 | CAAAATGGGTACACA[G/T]GCACCATGAACTATA | 7874 |
rs536058033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8934987 | TGAAAGCACAGGATA[A/G]CCACACACACAAGAA | 7874 |
rs536061814 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8911607 | ACAAATGAGAGCCCC[A/G]TGATGGGCCCAGCTC | 7874 |
rs536063701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8941880 | TCCTGGTCTCCTGGT[A/G]CTCACTAGGAAGTGG | 7874 |
rs536135447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8930994 | AAAAAAAAAAATCCT[C/T]AGGTAGTTCTTACTT | 7874 |
rs536233774 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961422 | GCTTGAACCCGGGAG[A/T]CGGAGGTTGTAGTGA | 7874 |
rs536250687 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8892842 | AATATACAGGAAGAG[C/T]TGGTGTACACTGCTC | 7874 |
rs536260200 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8913575 | GAGTTAAAATGTCTT[A/T]CACAACTGCAGATGA | 7874 |
rs536312964 | snp | C/G | 0.00159617 | 0.0282053 | downstream-variant-500B, nc-transcript-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8892022 | CCAGTTTAACAAACT[C/G]AAACTCCTGACACTG | 7874 |
rs536362780 | in-del | -/ACCT | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8949762 | TCCTTACGCAGAGAC[-/ACCT]ACCTTATCACTTCAT | 7874 |
rs536378173 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8945910 | GTAAAAATTAAAAAA[A/C]ACAACAGCACTGATT | 7874 |
rs536389614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8956301 | ACCCAAAGAGAATGA[C/T]CACCACCTTGAGAAT | 7874 |
rs536407496 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8902876 | GTGAAACTCTGTCTC[-/A]AAAAAAAAAGAAAAA | 7874 |
rs536407597 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8915733 | AACAGTTGAGGTTAA[A/C]CTTTTATACAGCCTT | 7874 |
rs536416783 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | USP7 | GRCh38.p7 | 16:8897159 | AAGGTCTGCTACCAC[-/A]AAGGAAGAGAGGAGA | 7874 |
rs536418992 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8924363 | GCTACACAAGCTTCT[A/G]AACGCTTCCTTTCAC | 7874 |
rs536420882 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937286 | AGGGTGGCTCACGCC[C/T]GTAATCCCAACACTT | 7874 |
rs536423671 | in-del | -/GCA | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8924226 | CCTTTGACAAACCCT[-/GCA]GCATCTTACTGCTTC | 7874 |
rs536483665 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8910055 | CATGAACTATATACA[A/C]TGGCAGGCTTTGTAA | 7874 |
rs536516227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961108 | CTGTAATATGAAAAT[A/G]AAGCTTCATTTTATG | 7874 |
rs536530940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8933099 | GTGTGTACCACCACG[C/T]TTGGCTAATTTTGTA | 7874 |
rs536540325 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8943165 | AAACTATTTGTTTGG[A/G]GCTTTCAGTTTAGCT | 7874 |
rs536570844 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8916200 | CAACGGGACAGCCAA[A/C]AAAGCCAGTCTTTGG | 7874 |
rs536614824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8926242 | CAGCACTTTGGGAGG[C/T]AGAGGCGGGCGGATA | 7874 |
rs536634654 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8897530 | TTTTCCCTCTATACT[G/T]GTAGAGCTAGAAAGG | 7874 |
rs536676749 | in-del | -/GACT | 0.00358779 | 0.0422022 | intron-variant | USP7 | GRCh38.p7 | 16:8959951 | CGACACTGAAACAGA[-/GACT]GACTGCTCACTTGGG | 7874 |
rs536693543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8928607 | TCCTACAGTCAGGAC[C/T]ACCTCCCTCCCACGC | 7874 |
rs536731101 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8928984 | CAAGAATTATCCAAG[C/T]TGCCATGAGAAGCTA | 7874 |
rs536731972 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8921697 | CACATGCTGGGGGAA[A/C]ACCAGCACCGGGGAG | 7874 |
rs536774466 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893467 | GGAGGAGGAGAACCC[C/G]AGGAAGGGCCGACAA | 7874 |
rs536793121 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8951925 | TCAGTGGCCCTGGAC[G/T]ATTCAGGCAGTGGGC | 7874 |
rs536842016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8943538 | GGGCCCCAATGCCAT[A/G]AGAAACACAAACGAC | 7874 |
rs536861963 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8946928 | CCATATTTTCCAAAC[A/G]GCCAATAAATGCAAC | 7874 |
rs536872299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8949073 | TGTGGTGATGAAAAT[A/G]TGCTCGAATTGAATG | 7874 |
rs536942950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8940061 | TGAGATCATGCCACT[A/G]AACTCCAGCATGGGT | 7874 |
rs536971348 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8913064 | GAAAAAACCTTAAAA[A/G]CACATGGGGGGCTGG | 7874 |
rs536973918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8917891 | GCCTCCCAGGTCCAC[A/G]CCATTCTCCTGCCTC | 7874 |
rs536976426 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8911337 | GCAAAATAGTAAAAC[G/T]TAACAATTTTTTAGG | 7874 |
rs537022921 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8930948 | CACTCCAGCCTGGCC[A/G]TCAGGGTGAGACTCA | 7874 |
rs537085063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8908140 | CCTGAGAGGGGAAAT[A/G]GACTCGGCAGAGGTT | 7874 |
rs537101725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8954240 | GAGGCAGAGGGAAGA[C/T]ACGTGCCCCCTGCGG | 7874 |
rs537105045 | in-del | -/G | 0.484054 | 0.087857 | intron-variant, frameshift-variant | USP7 | GRCh38.p7 | 16:8894531 | CCACACCAGCCCCCG[-/G]GGGGGGGAGAACCCT | 7874 |
rs537117366 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893899 | CAGCAGCGAATCCTC[C/T]TGCTGAAGACTTCGG | 7874 |
rs537126745 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8916379 | CTTTTTGTAGCCTAA[C/G]TCTGATCCTAAACAA | 7874 |
rs537131945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8926468 | TGGGCAACAAGAGCA[A/G]AAAACTCTGGTCTCC | 7874 |
rs537142990 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8936114 | AGAGTCCATGTCCTG[A/C]CACCAGGTGGTGCCT | 7874 |
rs537147781 | snp | C/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956662 | CAGCTACTCGGGAGG[C/G]TGAGGCAGGAGTATG | 7874 |
rs537157793 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964977 | ATTGACAGACTGATG[A/C]TTAGGGTCTCAACTT | 7874 |
rs537180875 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8898148 | GTTGGCTGCCGAATG[G/T]TTCCTTAGCTCCACA | 7874 |
rs537191710 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8958551 | AGCATGAGGCAGCAA[C/G]GGCCTGCTTTCAGGG | 7874 |
rs537199740 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8942738 | TTTTTTTGTAGAGAC[C/T]GGGTCTCACTATGTT | 7874 |
rs537215272 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8925470 | AGCTCTTTACAGGGT[C/T]TGATTTTATGTATAC | 7874 |
rs537239850 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, missense | USP7 | GRCh38.p7 | 16:8894442 | ACAGGTCGGCCAGTG[G/T]AGAGAGAGGAGCTGG | 7874 |
rs537284847 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8921100 | AAAAATCAAAAAGTT[A/T]AGGGAACAACAAGCA | 7874 |
rs537292601 | in-del | -/AC | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8959992 | ACACCAGGGAAAAAA[-/AC]AGTTTGTATGCAGAA | 7874 |
rs537308869 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8955389 | TGCTGGGATTACAGG[C/G]ATAAGCCACCATGCC | 7874 |
rs537347148 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8945097 | TCTGTACTAAATAAA[A/C]ATACAGAAATTAGCT | 7874 |
rs537384162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8949485 | GCAATTCCAATACAA[C/T]GGACATACCCAGGAC | 7874 |
rs537418100 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8928521 | TTTCACAACACACTT[A/C]TCCCCTGAAGAAGAG | 7874 |
rs537455113 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8926044 | CTGTAGTCCCAGCTA[C/T]TAGGGAGGCTGAGGC | 7874 |
rs537464409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8942492 | CTGTGTACTCTAAAA[C/T]GGGGGCCCTCCTAAG | 7874 |
rs537495410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8898856 | CAAAACACACAGCAG[C/T]CTGGCAGGACTGACC | 7874 |
rs537540069 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938376 | GAAAGAAATAATACA[C/G]TCAAGTCTTCCACAT | 7874 |
rs537552086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8904283 | GGGGTCCCAGAGGAG[C/T]GGGGACTGACCTGCA | 7874 |
rs537578204 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937840 | CAGGAGACAACTGGA[C/G]AAGAGAATTGCTCAG | 7874 |
rs537585525 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | USP7 | GRCh38.p7 | 16:8945391 | GCTGTCTCAAACAAA[A/C]AAACAAAAAGTTCCT | 7874 |
rs537630176 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962209 | AACTAAAGCATTCCA[A/C]GCCGTTTTCATTCAG | 7874 |
rs537633166 | snp | C/G | 3.31636e-05 | 0.00407194 | intron-variant | USP7 | GRCh38.p7 | 16:8899567 | ATTTGTCTTTCTGGA[C/G]TGGGATCTGAAGAGG | 7874 |
rs537637100 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8959505 | ATCATTAAAACCTGA[C/G/T]GTGCTCACATCAGAG | 7874 |
rs537654560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8933990 | TCAAACTCATGACCT[C/T]AAGTGATCTGCCAGT | 7874 |
rs537659346 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8932003 | AATTTCAGAGCCTTT[C/G]TGCCATCCGAACCAG | 7874 |
rs537712106 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957252 | CCTACGCATGACACT[G/T]AAAACCCTGCTTCCT | 7874 |
rs537725532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8922721 | CTAATTCATCTAAAT[A/G]GAAGGACCATCAAGA | 7874 |
rs537781481 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8896662 | CGTATCCTTCCTCTG[C/T]TTGGCTTTTCTATGG | 7874 |
rs537794732 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8927687 | CTAAAAATACAAAAA[C/T]TAGCCAGGCGTGGTG | 7874 |
rs537941892 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8933659 | GATTTTACAATGTTG[C/T]CCAGGTTGGTCTTGA | 7874 |
rs537945732 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8905870 | ACAGTGATGAACGCT[A/G]CTGTTACACGCACTC | 7874 |
rs537973037 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8916750 | GTTTCCAAGAAAATG[G/T]AATAAATCTGAAAGC | 7874 |
rs538020536 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8901869 | ACAGAACAGGACGGC[A/C]CCACGTGGCTGCTAC | 7874 |
rs538045486 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8906951 | TTTTAATATTCTACA[C/G]ACATCCTGAAATTGA | 7874 |
rs538100813 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8945542 | ACTAGTGATGTACTG[C/T]GAATGCTAGCCATTC | 7874 |
rs538119756 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8902995 | TACAAAAATAAAGAG[C/G]GGGTAGGGGTGCAGG | 7874 |
rs538130166 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8925688 | CACTGCCCTGACACA[C/T]AGTGGTTAGTTCACA | 7874 |
rs538131462 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8963007 | AATGCACGGGGCCGG[A/G]GTCCCGGCGGCCGCC | 7874 |
rs538158362 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8907409 | CAAGTAAAGTGATTT[C/G]ATTACACTCTCCCTT | 7874 |
rs538158440 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8902753 | ATCAGCTGGGCCTGG[C/T]GACGGGTGCCTGTAA | 7874 |
rs538183347 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956686 | GAGTATGGCTTAAAC[A/C]CAGGGGTCAGAGGTT | 7874 |
rs538200705 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8916390 | CTAAGTCTGATCCTA[A/C]ACAAAGATGGGCATT | 7874 |
rs538203763 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8920952 | CTCCCTTTGAATGTC[C/T]GACTAAAAAGTGAGA | 7874 |
rs538291485 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8925633 | GCTGCCCAGCCCCGC[A/C]GAGGCCACCGCGCAT | 7874 |
rs538294755 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8925330 | ACTACTAGCTTGCCC[A/G]CTTTATGAAGCCCAT | 7874 |
rs538322632 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8928042 | AAAATAGTGAATAAG[A/G]AACTAAAAGTAGAAT | 7874 |
rs538441324 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8909606 | CAACAGACCAGAATA[C/G/T]TTCTTCATCACACCA | 7874 |
rs538446521 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8914265 | CAAAATCTTTCAAAG[G/T]CTGGCAACTGACAGC | 7874 |
rs538451414 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8939435 | GACCATTCACTTGCT[C/G]ACATCTGGGTCCTTT | 7874 |
rs538527734 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8908268 | AAATATAAAGACTGA[C/G]GAAAGCACTGAGACT | 7874 |
rs538551483 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8909960 | TGATCTATACCTCAG[G/T]CCCTCAGTCCAACTG | 7874 |
rs538553440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8904685 | TGGTGGCTTACGCCT[A/G]TAATCCCAGCACTTT | 7874 |
rs538569360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8939473 | GAGGAAATTCACAAA[C/T]AAAGCTGCTATGAAA | 7874 |
rs538604634 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8954915 | CAGTGAGCCAAGATC[A/G]TGCCACTGCACTCCA | 7874 |
rs538621888 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8928238 | CAAATCAGTCAAGTC[A/G]CTGATAGTTTGGCTA | 7874 |
rs538630110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8932998 | CAGGCTGGAGTTCAG[C/T]GGCGAGATCTCGGCT | 7874 |
rs538685528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8922412 | AGAATCGCTTGAACC[C/T]GGGAGGTGGAGGTTG | 7874 |
rs538733420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8923680 | GTTCCACATGAGAAC[A/G]ATGTCTACTTTACTA | 7874 |
rs538800614 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8902758 | CTGGGCCTGGTGACG[A/G]GTGCCTGTAATCCCA | 7874 |
rs538853895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8941119 | GCTGCCCAATTCACA[C/T]GGGGCCCATGCCCCA | 7874 |
rs538865275 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8910887 | ATAATGTAGCCAACA[A/C]AGGTGTAAGTTATTT | 7874 |
rs538872574 | snp | C/T | | | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962642 | CCCGGGTCAGAACTC[C/T]GGGCCAGTCCAAAAC | 7874 |
rs538902425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8941994 | TGAAGGAGGAGACAA[C/T]TGGCAAGCACAGAGT | 7874 |
rs538914038 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant | USP7 | GRCh38.p7 | 16:8936677 | CTCACCCACATCAGA[A/G]TGACTGCATAGAATC | 7874 |
rs538920335 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8946781 | GCCAGCACGCAGAAG[C/G]CTCCACCTACAGAGC | 7874 |
rs539017961 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | USP7 | GRCh38.p7 | 16:8900206 | AAGACAGACTGAAAT[G/T]AATTACCCAAGTAGG | 7874 |
rs539042927 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8902656 | GCACTTTCGGAGGCC[G/T]AGGCAGGTGGATCAC | 7874 |
rs539052899 | in-del | -/TC | 0.00716266 | 0.059414 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893527 | ATTAGGTTGTGAGTT[-/TC]TCTGTTTTGCCTTAA | 7874 |
rs539073890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8934461 | GCATAACATCTTACA[A/G]GATGGGGTGGGGGAA | 7874 |
rs539123640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8930666 | TCTGCACAAAACTTT[C/T]TATATAAAATCTCTT | 7874 |
rs539155654 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8895214 | TCAAAGTGTCCACAT[A/C]TCAATTCTCACACTA | 7874 |
rs539166160 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8923722 | CCAAGGACCCCAGGC[A/T]CCAAGTGAGTGGAGA | 7874 |
rs539190401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8927348 | AAAGAAAGTTAAAGA[A/G]AAACAGAATACTTCA | 7874 |
rs539193242 | snp | C/T | 0.000164764 | 0.00907495 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8897013 | CCTAAGTTTCCCTGA[C/T]GCTTTCTCCCCAAGC | 7874 |
rs539202446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8951855 | GAAGCAATCTACCAA[C/T]GTGCGTTATTTTGCT | 7874 |
rs539231384 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8953509 | GAAGACACGTGCCCC[A/C]TGCGGTGCCACTGGA | 7874 |
rs539244022 | snp | C/G | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891719 | CTCCCTTGGGCTTTG[C/G]TCACAGCACGAGCCA | 7874 |
rs539262417 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8912459 | ATGTCAAAAAAAAAA[-/G]AAAGAAAGAAAAAAG | 7874 |
rs539287000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8926196 | AAAAAACAAAAGGTC[A/G]GCCGGGCGCGGTGGT | 7874 |
rs539301013 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8944226 | ATACGCAGAGCAACA[C/G]AGGTGCAAAAAAAAA | 7874 |
rs539338975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8915039 | TCCTGTGAGGAGAGG[A/G]GAGGTGGTGGCTGGG | 7874 |
rs539359526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8946531 | ATATCTGCAAATCGC[A/G]TATCTTACAAAGACT | 7874 |
rs539367946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8917232 | AGTAAGAATTTAATC[C/T]TCATGTTTAAAAAAA | 7874 |
rs539370115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8955525 | CAGGCCTGGCCAACA[C/T]GGGGAAACCGTCTCT | 7874 |
rs539492325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8897500 | CTACAAAGGTGAGGC[C/T]ATTTATGTCTCGAAT | 7874 |
rs539508613 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957829 | ACTTTACAAAATACC[A/G]AAAAGAAATTTTCAG | 7874 |
rs539517175 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8903554 | AAAACCGCATAAAAT[G/T]ACCAAAACCTAAATC | 7874 |
rs539571658 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8940001 | TACTTGGGAGGCTGA[A/G]GCACAAGAATTGCTT | 7874 |
rs539633395 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964862 | CATTTGGTATTAATT[C/T]ACTTCCTTCCTATCA | 7874 |
rs539648974 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8955674 | TCACACCACTGCACT[C/G]CAGCCTGGCAACAGA | 7874 |
rs539655670 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893321 | TTGAATTTAACAATG[G/T]TCTTGATTTAATAAA | 7874 |
rs539670416 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8948980 | GGGAAAAAAAAAAGC[C/T]TACACAGTCTATGAA | 7874 |
rs539673095 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964282 | CGGGGTTCAGGTCCC[A/G]GCCTAGCGCGCCGGG | 7874 |
rs539708081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8959427 | TACAGAGAAAAAATT[A/G]ATAATGAGGATATCA | 7874 |
rs539716023 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894405 | AACTCGTAGGTTATG[A/G/T]AATGCTATTGCTCCT | 7874 |
rs539744892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8958928 | TTCTTCCTAATCCAC[A/G]TCGGATATGGTTACT | 7874 |
rs539759525 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8954137 | ACACGTGCCCCCTGC[G/T]GCGCCACTGGAGGCA | 7874 |
rs539823636 | in-del | -/TG | 0.0162462 | 0.0886519 | intron-variant | USP7 | GRCh38.p7 | 16:8916000 | ACAGCCATTTCATGT[-/TG]TGTGTGTGTGTGCTT | 7874 |
rs539832788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8913020 | AACCTCAGGCAGCCA[A/G]AATCAAACAACTGAA | 7874 |
rs539849645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8917504 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGAATTAC | 7874 |
rs539861406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8941654 | AGCCTTGCTTGGTAC[C/T]AGGAAAGACAAAGAC | 7874 |
rs539871016 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8912637 | GAAGAAAGCAAAAGC[A/C]TACTAAGAAGAGACA | 7874 |
rs539907374 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8900347 | ATTGAGAAGAGCTTT[A/C]TGAGATGAAAATGTT | 7874 |
rs539921675 | in-del | -/T | 0.29046 | 0.246704 | intron-variant | USP7 | GRCh38.p7 | 16:8935202 | GAGCTAAGGCACTAA[-/T]TTTTTTTTTTTTTTT | 7874 |
rs539945077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8908034 | TTATTAGAAATCCTG[C/T]GAATGCAAGAGCTGT | 7874 |
rs539955795 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8905034 | AAGTCTGCATCGAAA[A/C]GCGCAAGCCCAACCC | 7874 |
rs539957049 | snp | C/T | | | intron-variant, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8949561 | ATCCTTACCTCCAAA[C/T]CCCCGAGCTCAAGTC | 7874 |
rs539979567 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8936900 | CCTTGGCTGTGACAA[A/G]TCTGGTTTAAAACAC | 7874 |
rs539991418 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8951001 | AAAAACTGATCTGAT[A/G]CAACGTCCCAAGAAT | 7874 |
rs539997352 | snp | A/G | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8931407 | CGGTCAACTGGTCTC[A/G]AACTCCTGGCCTCAA | 7874 |
rs540003101 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8904220 | AGCTCAGGAGAGCAC[A/G]TGGAGCAGCTTCTCT | 7874 |
rs540031411 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961142 | AAAGAAAGTAGCCTT[A/G]AAAACGTGCATGGAG | 7874 |
rs540035292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8895306 | AGTGATGGGCACTCA[C/T]GGGAGTCTCAGCCAG | 7874 |
rs540035882 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8935717 | GCTAGGCCTTTTAAC[A/G]CAATATGTATATGAA | 7874 |
rs540079321 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956920 | TTCTGGGCAGCACAA[C/T]ACAGACAAGTCGACG | 7874 |
rs540079801 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8932399 | AGTGAGACCTCATCT[-/C]AATTTATTATTATTT | 7874 |
rs540081250 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8930233 | GTACCAAGCATGGAT[C/G]TGAACCTGTTTTCTG | 7874 |
rs540117354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8952039 | GGTGAGGTAGGAAAA[C/T]GGATGAAAGCAGGAG | 7874 |
rs540121868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8927052 | GGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 7874 |
rs540159157 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8898787 | TTAATACTCCTGTTT[A/C]CCAAGAACTAAGTCC | 7874 |
rs540187912 | snp | A/C | 1.67964e-05 | 0.00289792 | intron-variant | USP7 | GRCh38.p7 | 16:8915221 | AGTAGAAATCATCAA[A/C]AGATCATGCCATTAG | 7874 |
rs540236354 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8936468 | TAAATTTTACTGATA[C/G]AATGTCTAGATGTAT | 7874 |
rs540260722 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8909720 | ATCACAAGGTCAGGG[A/G]TTTGAGACCTGCCTG | 7874 |
rs540308845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8919484 | ATTACACTTATCACA[C/T]GCAAGGTCAGCACAA | 7874 |
rs540345275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8911007 | TAGCACCTTTGCTCA[C/T]TGGCCAAAGGTCATT | 7874 |
rs540345340 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8915908 | TGACTGGTTTGTCCA[A/T]GGATATTTAATGAAC | 7874 |
rs540383177 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8922553 | GAACATGTTACTGAG[C/G]GTTCCAAAGGGCCAC | 7874 |
rs540409637 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8955599 | TAGTCCTGGCTACTT[C/G]GGAGGCTGAGGCAGG | 7874 |
rs540454419 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8911422 | TAAGAGTGAAAGGGC[A/G]AGCCACATGCTGAGT | 7874 |
rs540462890 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8901064 | GCAAGTCACCTAGGA[G/T]AAAGAAGATATTTTA | 7874 |
rs540463700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8905949 | AGGAGCTCGGTGCTG[A/G]CCCTGTGGTCTTGGG | 7874 |
rs540484231 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938115 | GCACTGCCACAAGAG[G/T]CCCTAGGCAGGAAGA | 7874 |
rs540522002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8929234 | CTCAACCGCTTTCGG[C/T]ATCTCAGATGTCTAA | 7874 |
rs540575443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8901549 | GACTGGCTGGAAGAG[C/T]GTTGCCACGGGAAGA | 7874 |
rs540606108 | snp | C/G/T | 0.00199529 | 0.0315338 | intron-variant | USP7 | GRCh38.p7 | 16:8933735 | GATTACAGGCATGTG[C/G/T]CACCCTGCCTGGCCT | 7874 |
rs540668061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8916949 | CTCTACTAACTTTTC[C/T]ATTCTCTACTCACTT | 7874 |
rs540719308 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8939848 | CTCACGCCTGTAATC[A/C]CAGCACTTTGGGAGG | 7874 |
rs540727172 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8943113 | TATGAAAACCAAGCC[A/C]CAAAGAAGGCCACAT | 7874 |
rs540744386 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8912774 | AAATAATTATAATTA[A/C]TTGATAAATACATAG | 7874 |
rs540745289 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8945960 | TTATGAAGCTTCCAT[A/T]ATCAAGACAGCACTG | 7874 |
rs540769408 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8942198 | CACTCTAAAATGTTC[A/C]CTCCCAGCAGGTGCT | 7874 |
rs540783981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8925966 | GAGACCATCCTGGCT[A/G]ACACGGTCAAACTCC | 7874 |
rs540852714 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8913079 | GCACATGGGGGGCTG[G/T]GCACGGTGGCTCACA | 7874 |
rs540860113 | snp | A/G | 1.64827e-05 | 0.00287073 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8903299 | CTCTGAACAAACTCA[A/G]CAAGCGAGGAGTTCT | 7874 |
rs540885893 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8896284 | ATTTGGGCACAGAGA[G/T]GTACAGACTGGGCCT | 7874 |
rs540920808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8934129 | TTCAAACTTACCCTA[C/T]GACAATAGCTTTAAA | 7874 |
rs540931976 | snp | C/T | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8904332 | TGCCCTGCTGCATGG[C/T]GACCTGGGAGTCCCA | 7874 |
rs540993363 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8927245 | GAGAATCGCTTGAAC[A/C]CGGGAGGCAGAGGGT | 7874 |
rs541028613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8926764 | TGCCACTAACATTAG[C/T]AGACCACCATTTCAT | 7874 |
rs541058229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8921761 | GCATCGACGAATTCA[C/T]GATGAGGCACAAAAT | 7874 |
rs541088328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8944843 | GGACACAGTGGCTCA[C/T]GCCTGTGATCCCAGC | 7874 |
rs541097495 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8958690 | CTATCTAGTGTTCCA[C/T]TTCCCCACACTCATC | 7874 |
rs541115983 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8910245 | CCAAGCGGGGGCTGG[C/G]CACCTGGTCGCCCAC | 7874 |
rs541143191 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937570 | TTGGGTGTGGTGGTG[C/T]ACACCTGTAATCCCA | 7874 |
rs541181996 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892629 | AAAAAAAAAAAAAAA[-/A]GAAACAAGAGACCCT | 7874 |
rs541205468 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8945274 | CTGTAATCCCAGCTA[C/G]TCGGGAGGCTGAGGC | 7874 |
rs541209392 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8908245 | AAATAAATCAGATGT[C/G]GGACTGAAAATATAA | 7874 |
rs541288253 | snp | A/G | 3.58153e-05 | 0.00423159 | intron-variant | USP7 | GRCh38.p7 | 16:8898667 | ACAGCATATAAATAA[A/G]TGACTTGTTTATTTG | 7874 |
rs541320861 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8903734 | TAGCTGGGTGTGGTG[G/T]CACATGCCTGTAATC | 7874 |
rs541343252 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8935569 | GGACATGTTTGGCAA[A/G]CACAAGTGACTATGT | 7874 |
rs541354874 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964484 | TGGCAAAGTTTGGCT[C/T]CTCAAGAGCAACCCC | 7874 |
rs541365590 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8945597 | GGGACATACCGTGCC[A/C]ATGGAGTGGGAGACA | 7874 |
rs541371917 | in-del | -/A | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8958056 | TCTCAGAGTACACTG[-/A]AAAAAAGTGTTTCCT | 7874 |
rs541401177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8940800 | CCCTGGAATATTAGC[C/T]GGACATGGTGGCGCA | 7874 |
rs541428898 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8933669 | TGTTGCCCAGGTTGG[G/T]CTTGAACTGGACTCA | 7874 |
rs541434748 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894269 | CTAAGGAGGCCCACA[A/C]CCTGACTGCGCCTCA | 7874 |
rs541444639 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8895488 | ACTAATTTCTGTGCA[A/G/T]AAACACTGTAGGTCC | 7874 |
rs541456588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961750 | TATGTTTTAGATGGG[C/T]TGCAAAATACAGCAC | 7874 |
rs541465391 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8965043 | TGGAGCAAACCGATA[C/T]ACATTTCTACACATC | 7874 |
rs541492700 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8922472 | CAGCCTGGCGACAGA[C/G]TGAGACTCTGTAAAT | 7874 |
rs541496449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8952621 | CTGGGGCATGCAGGC[C/T]CACCTCCTCACTAGG | 7874 |
rs541511878 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8892170 | ACTACAGCCAACCCC[A/C]AGCCCAGAACAAAAA | 7874 |
rs541515586 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8954702 | AATTGCAGGCCGGGC[A/T]CGGTGGACTCACACC | 7874 |
rs541540455 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8924980 | CCCTAATCCTTTTGA[C/G]GATAGAAGTCTACTA | 7874 |
rs541568624 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8904378 | ACCTGCACTTGTGTA[C/T]AGAGATGGGTGCCCG | 7874 |
rs541573568 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, missense | USP7 | GRCh38.p7 | 16:8894468 | GCTGGCACTTGACCC[G/T]GGGGCTGCCCCTCCC | 7874 |
rs541576276 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8911085 | AAGGTTTTACTGTTA[C/T]TCGAACAAAGCACAT | 7874 |
rs541609085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8952889 | TCGCCCAGGCTAGAG[C/T]GCACTGGCGCAATCT | 7874 |
rs541652379 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8918143 | CAAAGATTTGATTAA[A/C]AACTTAAATGTGACT | 7874 |
rs541653367 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8948828 | ACTTAGCCAGGCGTG[A/G]TGGCGTGTGCCTGCA | 7874 |
rs541839173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961224 | CCGGCCAGGCGCGAT[A/G]GCTCACACCTGTAAT | 7874 |
rs541845971 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8895835 | AATAAAGTTACCACG[A/G]TATGTTTTTTTTTTT | 7874 |
rs541846008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8901462 | CAGACCCATGGAAAC[C/T]CACTACATTTAGACA | 7874 |
rs541848444 | snp | A/G | 1.64939e-05 | 0.0028717 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8906468 | AACCACATAATGTCC[A/G]CCATGATTATCTCCA | 7874 |
rs541881729 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8896815 | AGACTTGAAAAACTG[C/G]AGCAACACTGGGTCT | 7874 |
rs541883254 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8911888 | ACCTTCAGAGCTCAC[A/G]ACAGGCTGGGAAGTC | 7874 |
rs541931550 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8934099 | ACGTACACCCAGTAC[-/T]TTTAACTTCCTTGGT | 7874 |
rs541960174 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8896188 | AATATCAGAAACAGA[G/T]ACCGGAGGCAAGGCA | 7874 |
rs541995395 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8916064 | TTTGCTAGTGATTAG[C/T]GATGGCGCGGGGAGA | 7874 |
rs542016844 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8897148 | AGAAAGCATAAAAGG[G/T]CTGCTACCACAAAGG | 7874 |
rs542047262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962648 | TCAGAACTCTGGGCC[A/G]GTCCAAAACCTGACA | 7874 |
rs542066331 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950828 | CAGTGATCTGAGCGG[A/G]CACTATTTGTCACTT | 7874 |
rs542135155 | snp | C/T | 1.71979e-05 | 0.00293235 | intron-variant | USP7 | GRCh38.p7 | 16:8921321 | GAATAATCTGAGCCT[C/T]AGTTGACATTATTTA | 7874 |
rs542158851 | snp | A/G | 4.95094e-05 | 0.00497517 | intron-variant | USP7 | GRCh38.p7 | 16:8916480 | CATTGTAAGAAATAT[A/G]CAAGTATTGCTTGAA | 7874 |
rs542203869 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8929869 | ATCCCTAACAGGAGC[A/G]GGGAGGGATTCATAG | 7874 |
rs542218263 | in-del | -/AAA | 0.261143 | 0.249752 | intron-variant | USP7 | GRCh38.p7 | 16:8901322 | CAAACAAAAAAACGA[-/AAA]AAAAAAAACAGTAAG | 7874 |
rs542273557 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8902802 | CTGAGGCAGGAGAAT[C/T]GCTTGAAACCAAAAG | 7874 |
rs542289031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8931324 | CTCCTGAGTAGCTGG[A/G]ATTAGAAGCATGTGC | 7874 |
rs542310303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8907020 | ACCAAATTTCACCAT[C/T]AGTGTTGCAAAATTA | 7874 |
rs542327010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962362 | ACCAACTCCCTAAAT[C/T]CAACACCCTTCTCTT | 7874 |
rs542331676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8930111 | ACTCTACTTACCTGG[C/T]AATGGTGTAGGCAAT | 7874 |
rs542332000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8934518 | CAGCAGTGGGATTAA[C/T]TGCAGTGTGATGACT | 7874 |
rs542345122 | snp | C/G/T | 0.00517822 | 0.0506191 | intron-variant | USP7 | GRCh38.p7 | 16:8939132 | ATTTACATGTACTTA[C/G/T]GTGTATTTAGTTCTC | 7874 |
rs542378212 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8965274 | GGGCCAGGTCGGCGC[C/G]GTGGCTCACACCTGT | 7874 |
rs542389632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8899920 | TGCCTGAGCTCCCTC[C/T]GTAAGCGAGGCAAGT | 7874 |
rs542392582 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8941264 | AAGTGGAAAAATTAA[C/G]TATGCTCAAACATAA | 7874 |
rs542438594 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8948796 | GCGAAACCCCGTCTC[C/T]AGAAAAAAAATACAA | 7874 |
rs542449150 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8904713 | TTTGGGAGGCTGAGG[C/T]GGGCCGATCACGAGG | 7874 |
rs542484443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8926249 | TTGGGAGGCAGAGGC[A/G]GGCGGATAACCTGAG | 7874 |
rs542505858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8948481 | TCAGCTGCCACACCT[A/G]GCCCCCAGTTAACTC | 7874 |
rs542549309 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961653 | GTAGGACAATGTCAT[A/G]GGAAATCCATATGCT | 7874 |
rs542564897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960397 | GTTTTCCAATGAATA[C/T]ACAAGGACTGTGCAG | 7874 |
rs542567466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8918947 | GGGAGGGAGACGCCA[C/T]GTTTGTTGAGAGGAC | 7874 |
rs542570243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8909246 | GGGGCCCTCACTCCA[C/T]GTCTGACTCACAGCT | 7874 |
rs542651626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8918682 | GCCGTGGTGGCGGGT[A/G]CCTGTAATCCCAGCT | 7874 |
rs542656192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8913513 | AGAAGACGGTAGAAC[A/G]TCTAACAGACCGAAG | 7874 |
rs542683789 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893217 | TGTCGTCTGTTCCAC[-/T]TTTAACGAAATTCTA | 7874 |
rs542720925 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8894957 | ACCCCAGCAGGAGCG[A/C]AGATTCGGCAACAGC | 7874 |
rs542727413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8914691 | GGGAGCCCAAGGCAG[A/G]AAGGTTGCTTAAACC | 7874 |
rs542736935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8931872 | ATGCTGGCCCCACGG[C/T]TGCCTACACAGTCGG | 7874 |
rs542835797 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937063 | AAGGCAAAGTACAAT[A/G]CCCTCTCAGCCTAAC | 7874 |
rs542842866 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8910948 | GTAAACAACACTAAC[A/C]GTAACTCTCCCCCTG | 7874 |
rs542847948 | in-del | -/A | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8958218 | AAGTGCATGGGTCTT[-/A]ATGCAAGCCAACAGG | 7874 |
rs542864072 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8907662 | GCCTGGCCAGCATAG[C/T]GAAACCCTGTCTCTA | 7874 |
rs542875702 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | USP7 | GRCh38.p7 | 16:8942050 | TGCAAGAAGCCTGCC[A/G]GCCAGAGATGGAAAA | 7874 |
rs542903377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8933329 | AGACGGGACGATCAC[A/G]TAAGTCAAGGAGTCC | 7874 |
rs542916881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950647 | CAGCCCTGTCTGCCA[C/T]GAACATGGCACTGCT | 7874 |
rs542948394 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937400 | TACAAAAATTAGCCA[A/G]ACGTGGTGGCGCATG | 7874 |
rs543029552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8951478 | GCTCACCCACCTCGC[C/T]CTGAGCCAGCCGGAT | 7874 |
rs543057952 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891711 | CATAGTGTCTCCCTT[C/G]GGCTTTGCTCACAGC | 7874 |
rs543106714 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964810 | ATAGTGATAATAAAA[C/T]AATAATATAAAAATA | 7874 |
rs543108879 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8943808 | TCCCCAAGAAAATGA[A/G]CATTCACGCTGGGGG | 7874 |
rs543138186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8916887 | ATGATAAAAGCACTG[A/G]CACGATTAAATGCTC | 7874 |
rs543195044 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8905124 | AAAGGATATTGGAGA[C/T]TCATGGTACAAATGT | 7874 |
rs543196362 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8920583 | CCCAACTTTTTTGCT[A/C]ATTTTAGACTGTTTC | 7874 |
rs543196622 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8948415 | ATCTCAAACCCCTGG[C/G]CTCAAGCTATCCACC | 7874 |
rs543208962 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893092 | AAATTGTACATGTTC[A/G]TTCATTAAATATACA | 7874 |
rs543233697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8910493 | GAGGAACGGGGAAAG[A/G]ACAAGATGCCTAAAA | 7874 |
rs543242006 | in-del | -/AAAG | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938350 | CAGTCAAAAAAAAAA[-/AAAG]AAAGAAAGAAAGAAA | 7874 |
rs543262754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8917334 | TACAAAATCATGAAC[A/G]TCTTTAGGGATACTG | 7874 |
rs543305290 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8935145 | TATATGCCACCTTTT[C/T]GGAAGTTTTTAAGAC | 7874 |
rs543306392 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8900898 | TAGCTGGTAGACCTA[A/T]CACTGTAACAAATTC | 7874 |
rs543344357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8939822 | AGACTGTTTCTGGCC[A/G]AGCGCAGTGGCTCAC | 7874 |
rs543396583 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8892945 | ACTCAAAACTAGACA[C/T]GCAGCTGGCATTAGC | 7874 |
rs543414710 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8925899 | GTGGCTCACTCCTGT[A/C]ATCACAGCACTTTGG | 7874 |
rs543417742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8935511 | CCACCATGCCCAGGC[C/T]ATGGCACTATTTTTG | 7874 |
rs543447818 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8958348 | TGTGTGCTGGGAACC[A/G]GCAGCACCAAGGAGG | 7874 |
rs543458184 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8930804 | TGAAACCCCGTCTCT[A/T]CTAGAAATGCAAAAA | 7874 |
rs543463867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8948731 | GCAGCCAAAAACAAG[C/T]ATGGACAACACAACG | 7874 |
rs543472712 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP7 | GRCh38.p7 | 16:8930798 | ACATGGTGAAACCCC[A/G]TCTCTACTAGAAATG | 7874 |
rs543484077 | snp | C/T | 0.00597247 | 0.0543191 | utr-variant-5-prime, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8963444 | CGGCCCCGGGGCGGC[C/T]CGCGGCGGGCGGCGG | 7874 |
rs543485384 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8954461 | CTGCATTCGGGTCAT[C/G]GGCAATGGGACCACA | 7874 |
rs543486970 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8914936 | AGCGAAATAAACAAA[A/C]AAATACATCCTACTA | 7874 |
rs543547137 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8948393 | TTTCACCATGTTGCC[C/T]AGGCTGATCTCAAAC | 7874 |
rs543548985 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8949875 | TCTAAGAAGTTATTA[C/T]ATGAAAATGCTTGGC | 7874 |
rs543560523 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8917235 | AAGAATTTAATCTTC[A/G]TGTTTAAAAAAATCA | 7874 |
rs543567847 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893707 | TGAGCCAGGGACCCC[C/T]GATCCACTAACCTCT | 7874 |
rs543591490 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8954682 | TTGCGTAGTTTAATA[A/T]CAGCAATTGCAGGCC | 7874 |
rs543595733 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8949334 | GAGACATAAAAATGC[A/C]ATGCAATTGATTGTT | 7874 |
rs543605234 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8907132 | CAGCTCACAGCCCCT[A/G]CGGCCTTCAGGAATG | 7874 |
rs543634778 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8952445 | CACCGGGCTAAAACC[-/A]AGGTGCCAGCAGGGC | 7874 |
rs543722021 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8907626 | TTTGGGAGGCTGAGG[A/C]CGGCAGATCACTTGA | 7874 |
rs543774082 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8913259 | TACTTGTGAGCCTAA[C/G]GCAGGAGAATCACTT | 7874 |
rs543780174 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956511 | GGCCCACGCCTGTAA[C/T]CCCAACACTTTGGGA | 7874 |
rs543788286 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8900240 | ATTCTAAGGAGTTTC[C/G]ATTTCATAAATCTCA | 7874 |
rs543794372 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964395 | TTGTCGTTACTTACC[C/T]TTGCCCGCTGACGTG | 7874 |
rs543805516 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960631 | TAGTTCGTTAGGAAC[C/G]GAGGCAGACACTGAA | 7874 |
rs543810077 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8944974 | TTAGCTGGGTGGACC[A/G]GGCGCAGTGGCTCAC | 7874 |
rs543822122 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937378 | AAAACCCCATCTCTA[A/C]TAAAAATACAAAAAT | 7874 |
rs543829623 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8906975 | AAATTGACTTAGTTT[G/T]AACTGGCTCTACAAA | 7874 |
rs543861049 | in-del | -/A/C/T | 0.00368715 | 0.042805 | intron-variant, frameshift-variant | USP7 | GRCh38.p7 | 16:8894533 | CACCAGCCCCCGGGG[-/A/C/T]GGGGGAGAACCCTTA | 7874 |
rs543876343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8956083 | CAGTTTAACAACTTA[C/T]TGTGAGAGCTGGAGG | 7874 |
rs543904176 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8958633 | GCAGAGTTCAAAGCC[A/G]ACTCCCAACGTCTGG | 7874 |
rs543927391 | snp | C/G/T | 0.000158357 | 0.00889683 | intron-variant | USP7 | GRCh38.p7 | 16:8895787 | AATGAAGTATATATA[C/G/T]TCACATAAAAATAAA | 7874 |
rs543939758 | in-del | -/T | 0.00716266 | 0.059414 | intron-variant | USP7 | GRCh38.p7 | 16:8929044 | CCAAGACCTCCCCCC[-/T]TAAAAAAAAAAAGAA | 7874 |
rs543948751 | snp | A/C | 3.30415e-05 | 0.00406444 | intron-variant | USP7 | GRCh38.p7 | 16:8898511 | TTATGACCCATAGTT[A/C]CATTAATTTGGACTC | 7874 |
rs543980298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8900835 | GGTAAAAAAAAAAAA[C/T]TCACAAATCTAAATA | 7874 |
rs543989003 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956536 | TTGGGAGGCGGAGGC[A/G]GGCAGACTGCCTGAG | 7874 |
rs543996126 | snp | C/T | 0.0023933 | 0.0345097 | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891825 | GGGCCACTGTGACCG[C/T]AGGCCCTTGCTGTCA | 7874 |
rs543998034 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8922403 | CGAGGCAGGAGAATC[A/G]CTTGAACCCGGGAGG | 7874 |
rs544027642 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8954946 | CCCTGACAACAGAGC[A/G]AGACTCCATCTCAAA | 7874 |
rs544052003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8945221 | AAGAGCGAAATTCCA[C/T]CTTCAAAAAAAAAAT | 7874 |
rs544070739 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8922202 | ATTAAAGAAAATGAA[A/G]GTACGGCCAGGTGCG | 7874 |
rs544112696 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8918077 | TTACAGGCATGAGCC[A/G]CTGCGCCCAGCCATG | 7874 |
rs544113840 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8946363 | AGGCAGGAGGATCAC[C/T]TGTGGCCAGGAGTTC | 7874 |
rs544131431 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, nc-transcript-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8892076 | GAACGCGGCAGATGA[C/T]GGAAACATTACAACA | 7874 |
rs544174940 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8900384 | ACCTAATTTCAAAAC[A/C]CAGAGAAAGCCTCTC | 7874 |
rs544201494 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8904749 | AAATCAAGACCATCT[C/T]GGCTAACATGGTGAA | 7874 |
rs544215858 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8932723 | TATGAGATTCATAAA[A/T]TGTAAACCAAGGACA | 7874 |
rs544241946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8911491 | GTGTATGGAGAGCTC[A/G]TCCTGCTCCGGTCAT | 7874 |
rs544257886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8905076 | GCGCTGCTGTGAATA[C/T]AATGGAATAAGCATA | 7874 |
rs544310704 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8895324 | GAGTCTCAGCCAGAA[G/T]ATATCCAAGTTTCTT | 7874 |
rs544323631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8906075 | AACAAGGTAGGACCA[A/G]GGGGCACGCAGAGGG | 7874 |
rs544330732 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8916008 | TTTCATGTTGTGTGT[C/G]TGTGCTTCTGCGTCT | 7874 |
rs544358369 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8919946 | TACTCCTCGCTCACC[A/G]TGTTAGTTGTCGGTG | 7874 |
rs544378537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8952101 | CTATACAAAAAAGAA[A/G]AAAAATGGCCAGGTG | 7874 |
rs544398757 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8902254 | AGAGCGAAAAACTAC[A/G]GTCAAGTATTGAAGA | 7874 |
rs544414534 | in-del | -/TTGGAAAATAATTATTTTTTATACAACATTACTTGGAAAATAATTA | 0.021333 | 0.101051 | intron-variant | USP7 | GRCh38.p7 | 16:8947250 | CCTCTCAATACACTT[lengthTooLong]TTGGAAAATAATTAT | 7874 |
rs544426093 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP7 | GRCh38.p7 | 16:8924399 | GTACCTATCTCATTA[C/T]AGTCTGCACACAGCT | 7874 |
rs544436714 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8906364 | GAACCAGAACAGGCT[A/G]AAGCAGAGCTTGTGT | 7874 |
rs544454186 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8914849 | GCCTGAGTCCTGGAG[A/T]TCGAGGCTGCACTGA | 7874 |
rs544478120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962318 | TTTGTTTCAGTGAAA[C/T]GGGTCGTGAGAAAAA | 7874 |
rs544498572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8934178 | GATGCAAAAATGAGG[A/G]CTCATTTTCTGTACA | 7874 |
rs544499979 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8925462 | TATAATTCAGCTCTT[C/T]ACAGGGTTTGATTTT | 7874 |
rs544515609 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8948491 | CACCTGGCCCCCAGT[G/T]AACTCAACTTAGTAA | 7874 |
rs544533428 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892598 | AGTAAATGTGACTAG[C/T]TAGAGGCTAAAAAAA | 7874 |
rs544537816 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8928719 | ATTACTCAACCTTCT[C/T]GGATTATACGCTTTT | 7874 |
rs544611057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8930068 | TAAATTTAAACCTAC[A/G]TTACACCTCCTTGCC | 7874 |
rs544687032 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8933792 | ATGGAGTCTTCCTCT[A/G]TCTCCCAGGCTGGAG | 7874 |
rs544713846 | snp | C/G | | | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962710 | GTAAGCCCGACGCTA[C/G]GCAGTGCTGTTAGAA | 7874 |
rs544797617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8913477 | GACACTACAGCCCAC[C/T]TCTCAGAAATGAGGC | 7874 |
rs544877491 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8912587 | GACAGAATTAGTAGA[C/G]AAGAGCATTATCAAC | 7874 |
rs544884713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8930461 | ATAGAATAAGCAAAA[C/T]ATAAACTTATACTTT | 7874 |
rs544894095 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8948009 | CAGGCACTTTGGAGC[A/G]CAGCACTGCCTGGCT | 7874 |
rs544894575 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957447 | ATTTGTTACTCATGC[A/G]AAAAACCATAAACGG | 7874 |
rs544897997 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8927299 | TGCACTCCAGCCTGG[A/C]CAAAAAGAAAAAAAG | 7874 |
rs544930960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8932607 | AATCAAATATACATG[C/T]TAAATTTAAAAAAGA | 7874 |
rs544971740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8923011 | GCTGGTAGATTCTAA[C/T]AAACTATTTTTAGTT | 7874 |
rs545027704 | in-del | -/A | 0.000500988 | 0.0158191 | intron-variant | USP7 | GRCh38.p7 | 16:8923417 | CCAACTGGTGTCTGC[-/A]AAAAAAAACACATCA | 7874 |
rs545067647 | snp | C/T | 4.94311e-05 | 0.00497123 | intron-variant | USP7 | GRCh38.p7 | 16:8894752 | CTTGAGCCTATGGCC[C/T]GCCAAGCCCCCAGGA | 7874 |
rs545103707 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8958587 | CTGAGACAGCCAAAC[A/G]GGCCTGGCAACAGGA | 7874 |
rs545137417 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8951272 | TCTTTAAAATCTGGC[A/C]TCTTAAGTCACCTAA | 7874 |
rs545165438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8945128 | GGGTGTGGTGGCGGG[C/T]GCCTGTAATCTCAGC | 7874 |
rs545177221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8941370 | ATATCCTGCAGTCTG[C/T]GGTTAACAACTTTTT | 7874 |
rs545187053 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8965184 | TTCATCTCCCTTCCC[C/T]CCGAAAGAATGTTTT | 7874 |
rs545189255 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8940494 | GATCAGAGTGGGAGG[A/G]CAGGGGTTACCTTGG | 7874 |
rs545189420 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960457 | GAATGTGAGGCCGGA[C/G]AGCAAACTCACACTG | 7874 |
rs545209396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8935896 | TACCCCACCAGAGAA[C/T]ACCTCCCAATCGCTA | 7874 |
rs545224178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8941570 | TTTTTGTCCACGCAC[A/G]ATAGCAACATCAGAG | 7874 |
rs545243979 | snp | A/G | 3.33272e-05 | 0.00408197 | intron-variant, missense | USP7 | GRCh38.p7 | 16:8894520 | TAGTCTGAAACCCAC[A/G]CCAGCCCCCGGGGGG | 7874 |
rs545251662 | in-del | -/AAAA | 0.00716266 | 0.059414 | intron-variant | USP7 | GRCh38.p7 | 16:8901296 | CAATGCTTAAAAAAC[-/AAAA]AAACAAACAAACAAA | 7874 |
rs545252624 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8936962 | CAACCCGAGAAAGTC[A/G]CTGGGGGGCACACAG | 7874 |
rs545296358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8959794 | AGTAACTGCACAAGT[C/T]TGGAAGAAACCCACC | 7874 |
rs545326075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8918892 | ACTGGGGAATGAAAA[C/T]GCAGCATGAACTAGC | 7874 |
rs545333427 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8959149 | TCACAACAACCTTGA[C/T]GGGCATGAATGACCT | 7874 |
rs545365805 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8925324 | AATGAGACTACTAGC[A/T]TGCCCGCTTTATGAA | 7874 |
rs545371666 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8922617 | AGTCCAAGTCAGCAG[A/C]TTCCCCTGGTTCCAA | 7874 |
rs545387165 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8919957 | CACCATGTTAGTTGT[C/T]GGTGATGCTCACCTC | 7874 |
rs545404670 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8955182 | TACATTTGTTGTATT[C/T]AATAAACTTGGGTTT | 7874 |
rs545409568 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8948654 | AATATTATTCTGCGA[C/G]AAAAGGGAACGACTA | 7874 |
rs545465425 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8918603 | TAGCTTGGGGTCAGG[A/G]GTTCGAGACCAGCCT | 7874 |
rs545533265 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8925677 | CCCGAGTGTGGCACT[G/T]CCCTGACACACAGTG | 7874 |
rs545565635 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8920677 | CAGAGGTACCCAGGG[G/T]CTCAGTGCCACAGCA | 7874 |
rs545576773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8909791 | ATTAGTTGGGCATAG[C/T]GGCGGGCGCCTGTAG | 7874 |
rs545585949 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8952953 | GCGATTCTCCTGCCT[C/T]GGCCTCCCAAGTAGC | 7874 |
rs545586535 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8932058 | GACAGTGCCATGCTC[A/G]CCTCCCCCTCCAAGA | 7874 |
rs545628339 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8913996 | TCCCGACTCAGCCTC[C/G]CAAAGTGCTGAAATT | 7874 |
rs545632157 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8940489 | CTGTTGATCAGAGTG[G/T]GAGGGCAGGGGTTAC | 7874 |
rs545647555 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8939144 | TTACGTGTATTTAGT[G/T]CTCTACAATTTTATT | 7874 |
rs545733759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8943776 | ACTCATTTTGAAATG[C/T]TACCACAAAAACCCA | 7874 |
rs545810010 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8896719 | TGTTATCAGAAGATA[A/C]AAGGGGAAGGAGGAA | 7874 |
rs545810430 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956707 | GTCAGAGGTTGCAGT[A/G]AGCCGAGATCGTCCC | 7874 |
rs545811891 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8892225 | AGACAAACCCACAGC[A/G]AACGGCTCTCGCACC | 7874 |
rs545898856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8934529 | TTAATTGCAGTGTGA[C/T]GACTAAAGAAAGCCT | 7874 |
rs545907874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8963091 | GCCAGGCCGAGGCCC[A/G]GCGGCCGCCCGGGGC | 7874 |
rs545909827 | snp | C/G | 0.5 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8953852 | GGCAGAGGGAAGACA[C/G]GTGCCCCCTGCGGCG | 7874 |
rs545959009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8948339 | AAGCACACGCCATCA[C/T]GGCTGACTAATTTTT | 7874 |
rs545977674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8958605 | CCTGGCAACAGGATG[C/T]GGGATAGAGACAGCA | 7874 |
rs545978996 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8911923 | TTCCCACCAGCCACC[A/G]TGGAAAAACCGCTGA | 7874 |
rs545982066 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893663 | GGCAGCCGAGCCACT[C/T]GTGCCCACTAGGGAC | 7874 |
rs546000803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8897233 | TTCTTGCTCTCATTC[C/T]CACCCCAACTCCCTC | 7874 |
rs546001103 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8901534 | TCTGAGACCTGGACT[A/G]ACTGGCTGGAAGAGC | 7874 |
rs546072910 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8953709 | CACGTGCCCCGTGCG[C/G]CGCCACCGGAGGCAG | 7874 |
rs546139708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8959387 | GATACCTTCTTCCTA[C/T]ATTTACTAGTATCGA | 7874 |
rs546162697 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8917411 | TGACACGAAGTCTCA[A/C]TCTGTTGGCCAGGCT | 7874 |
rs546164461 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8965135 | CATCTCCCTATACCC[A/G]CTTTCCCTGCATTTT | 7874 |
rs546212823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8907577 | AAAACTACTTGTGGC[C/T]GGGTGTGGTGGTTCA | 7874 |
rs546262308 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8899336 | AAACTATATTATTCC[A/T]TAATGAATCACCATG | 7874 |
rs546277208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8930777 | AGTTCGAGACCAGGC[C/T]GGCCAACATGGTGAA | 7874 |
rs546317865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8958906 | GCTTAGGCAGAGGCC[A/G]GATGGCTTCTTCCTA | 7874 |
rs546335582 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8929271 | ACCTCCAAAAGCCCA[A/G]CAACCAGCGAGACCA | 7874 |
rs546354224 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8930530 | CAATAAAGATTCATT[C/G]TAATCCAAAAAATAT | 7874 |
rs546361497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8913742 | GCACTTCCCCTCCTC[A/G]CTCTTTTTATTTTAT | 7874 |
rs546392954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8921818 | TGCAGTGAAGTGTGG[A/G]GTGGACCACAAAAGG | 7874 |
rs546431596 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8926257 | CAGAGGCGGGCGGAT[A/C]ACCTGAGGTCAGGAG | 7874 |
rs546471178 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950670 | GCACTGCTAATTGTC[C/G]AAGATTCAGAAGCTG | 7874 |
rs546481583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8954352 | GAAATCTGACTCTGC[C/T]GCAACATCCAAACGT | 7874 |
rs546505501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8922147 | GAGGACAACTTTAAC[C/T]ATCCACAGGCCCTGG | 7874 |
rs546601834 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8904367 | GGTGGGGGCTGACCT[A/G]CACTTGTGTATAGAG | 7874 |
rs546633709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8909950 | AGCAACTTTCTGATC[C/T]ATACCTCAGTCCCTC | 7874 |
rs546642414 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8931908 | CCTGGTGCACTGGAC[A/G]CCAACAGAAATTAAG | 7874 |
rs546752149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8927484 | TAGTCAATCCCCACA[A/G]ATTAGTTTCATGGAG | 7874 |
rs546803638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950052 | GAGCGCTTGAAACAT[A/G]GCTGTTGTGACAGAG | 7874 |
rs546818746 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937186 | ATCCCTTTAGCCTGG[G/T]CAACACAGTGAGACT | 7874 |
rs546888726 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8924578 | GTAAAGAGTGCCTAA[C/G]AACATCCTCCCATCC | 7874 |
rs546922575 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8900477 | TTGGTTCTACAACTT[A/T]AAAAAATCCTGAAAT | 7874 |
rs546925416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8923909 | AGCACTGCTCAGAGG[C/T]AAGACAAGGGCTACA | 7874 |
rs546930260 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8904921 | AGCTTGCAGTGAGCC[G/T]AGATCGCGCCACTGC | 7874 |
rs546945510 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8912387 | CCCAGGAGACAAAGG[G/T]TGTAGTGAGCTGAGA | 7874 |
rs546951008 | snp | A/G | 7.20695e-05 | 0.00600246 | utr-variant-5-prime, intron-variant | USP7 | GRCh38.p7 | 16:8936646 | GTGGCCTCTGCTGGG[A/G]GATGGGGGAGGTTCT | 7874 |
rs546961198 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8942049 | GTGCAAGAAGCCTGC[C/T]GGCCAGAGATGGAAA | 7874 |
rs546997393 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8920787 | GTAACATTCCTAAGA[C/T]TGTTCCACTGGTTAC | 7874 |
rs547008262 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | USP7 | GRCh38.p7 | 16:8921072 | CTGACTCTAAAATCA[-/T]ATAAAGGACTTGAAA | 7874 |
rs547013027 | in-del | -/TAAG | 0.00358779 | 0.0422022 | intron-variant | USP7 | GRCh38.p7 | 16:8948502 | AGTTAACTCAACTTA[-/TAAG]GTAAGTGAAGCATAT | 7874 |
rs547032874 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8906758 | ATAGAAATAACTATT[C/T]CTAGTCAACATAAAT | 7874 |
rs547067907 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8934259 | AGTGTGGAAAATAAT[C/T]GAACTCTACAACTGC | 7874 |
rs547112657 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8911247 | CTCAGAGGTCAACAC[A/C/G]GGGTGGGGTGGAAGT | 7874 |
rs547117607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8932479 | AGACCATCATGTCTT[A/G]ACAGAAATACTGTGG | 7874 |
rs547125373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8955867 | TTTGCTCAGCCTACA[C/T]ATTCAGAGGAATGCC | 7874 |
rs547162621 | snp | C/T | 1.67764e-05 | 0.00289619 | intron-variant | USP7 | GRCh38.p7 | 16:8903224 | CGGAAGGAAGGTGGA[C/T]GTTGGGAGCCACGGT | 7874 |
rs547197820 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8895483 | TGAGGACTAATTTCT[C/G]TGCAAAAACACTGTA | 7874 |
rs547225750 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957784 | AAAAACAAAAAAAAA[G/T]TAAAAACACAAAAAC | 7874 |
rs547271437 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891886 | AGACTCCGAATGCTG[C/T]CAACAGATGGCATCC | 7874 |
rs547323980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8930887 | GGAATGAAAATCACT[C/T]GAACTCAGGAGGCGG | 7874 |
rs547337639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8895878 | GTCTCAATCTGTCGC[C/T]CAGGCTGGAGTGCAA | 7874 |
rs547337775 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891686 | CGTTGCAGGGGACTC[C/T]GCCAGGTCCCATAGT | 7874 |
rs547345395 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8943937 | ATTAAATTTATTGTA[C/T]TGCTTATTCTACAAT | 7874 |
rs547365445 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8909245 | AGGGGCCCTCACTCC[A/T]TGTCTGACTCACAGC | 7874 |
rs547392969 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP7 | GRCh38.p7 | 16:8953502 | TTGGGGAGAAGACAC[A/G]TGCCCCATGCGGTGC | 7874 |
rs547412693 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8913525 | AACGTCTAACAGACC[A/G]AAGGAAGGAACCTGC | 7874 |
rs547473434 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8915599 | AATTTTATAATTGAC[C/T]AGAAATATCAATGTT | 7874 |
rs547487166 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8907214 | ACATTTATGTGAAAT[A/C]TCACAATTTAAAAAA | 7874 |
rs547488691 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8944745 | GGACCTACTCAGACT[C/G]TCATGGAACACCTGC | 7874 |
rs547508047 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8939249 | CAGTGGCCCTGTTAC[G/T]ACCACCCACCCCGGC | 7874 |
rs547650556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962755 | GCGCTTCCGAGCCAC[A/G]GCGCGCCCTCCGGGG | 7874 |
rs547662973 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964767 | TGCACTCCAGCCTGG[A/G]CAACAGAATGAGACC | 7874 |
rs547675457 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893780 | ATAAAATAACTCTCA[C/T]TGGCATCCAAGCTTT | 7874 |
rs547688166 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8958404 | GTGCGACTTCCTGTA[C/G]AGAAGGCAGGACACC | 7874 |
rs547716891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8907998 | CTCTGAAATAACATT[C/T]ATAATCGGTCAAAAT | 7874 |
rs547735176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8936036 | GATTTATCAATCCTC[C/T]CCCAAAAAGCTGGCA | 7874 |
rs547735750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8898050 | CCCTGAGATCAGGCC[A/G]CGGCAGGAAGAGCTG | 7874 |
rs547774347 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8951626 | ACTTAGGTCTAAAAT[G/T]CTGTAATATCTAACT | 7874 |
rs547777895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8917464 | GCTCACTACAACCTC[C/T]GCCTCCTGGGTTCAG | 7874 |
rs547779315 | in-del | -/AACTC | | | intron-variant | USP7 | GRCh38.p7 | 16:8946597 | TCAACAGCTGGACAA[-/AACTC]AACTAAAAAGTCAGA | 7874 |
rs547802859 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8897357 | AGCCTGTCATTTACA[A/G]AACACCTTCTCAGGA | 7874 |
rs547875982 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950500 | TTCCTCTCCAGACCC[C/G]TTACCCCAAGGCAAT | 7874 |
rs547883576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8952124 | GCCAGGTGTGGTGTG[C/T]CTGTAGTCCCAGTCA | 7874 |
rs547895630 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8908520 | CAATGAAAGCAACAG[C/T]GGTTCAGCAAGATTG | 7874 |
rs547927120 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8908794 | AAACACTGTGCAAAT[G/T]ATGGAGAACCACAGA | 7874 |
rs548057131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8942354 | CCTTGCCAAATATCA[A/G]GCAGTGGGGTCTGTC | 7874 |
rs548062836 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8951538 | GAGCCCCTGGATATC[A/C]TATTTGCTCATCTGT | 7874 |
rs548115484 | in-del | -/A | 0.471511 | 0.115901 | intron-variant | USP7 | GRCh38.p7 | 16:8944233 | AGCAACAGAGGTGCA[-/A]AAAAAAAAAAAGCAC | 7874 |
rs548147141 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8940991 | CTCTCTCCTCCCACT[C/T]CAGGACCCTTCTTCT | 7874 |
rs548171268 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8919196 | CCATTGCTCCTGCAG[C/T]GTGTGTGAAGCAATC | 7874 |
rs548201975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8905756 | TTTTATCCTATCCCA[C/T]GGCATTTTATGGAAG | 7874 |
rs548205006 | snp | C/T | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8901192 | CAGTAATTCAAGCTC[C/T]GCGTTTTGGGATCAT | 7874 |
rs548238312 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937554 | CTCAAAAAATAATAA[A/G]TTGGGTGTGGTGGTG | 7874 |
rs548282057 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8919759 | CCACCTCCACGCCCA[A/T]CTCCCTCTGTACACA | 7874 |
rs548288186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8914963 | ACTACAAGGTTCTAT[C/T]TAAACAGACACCTAA | 7874 |
rs548299413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8896474 | ATTTGTCCTCCAAGC[A/G]ACTACAGGGCAAAGT | 7874 |
rs548309636 | in-del | -/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8952838 | TGTGACCACACTCGC[-/T]TTTTTTTTTTTTAAG | 7874 |
rs548384073 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8925113 | TTAAGTTCTGCAAGG[C/T]AGACAAGAGACAGAT | 7874 |
rs548426764 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938288 | AAACTTTTCTTGATT[A/G]AACTTTGAGATAACT | 7874 |
rs548477943 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8955086 | CACCTATACCCACTT[C/T]CTATGAATCTGCAGT | 7874 |
rs548556563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8898198 | CTCAGGAGGTCCTGC[C/T]AGGAGGCAGGAAAGA | 7874 |
rs548556752 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8901935 | CAGTCTTATTTGACT[G/T]CATCAGGAAGTCTAG | 7874 |
rs548615617 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8933959 | ACAGGGTTTCACCAT[G/T]TTGGCCAGGCTGGTC | 7874 |
rs548615873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8929110 | GTGGGAACTAGACCC[A/G]GAATGTTCCGATAGG | 7874 |
rs548630480 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8933900 | AGCTAGGATTACAGC[C/T]GTGTGCCACCACGCC | 7874 |
rs548716257 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8924379 | AACGCTTCCTTTCAC[C/T]TTCTGTACCTATCTC | 7874 |
rs548729947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8908592 | AGGTGTCCATTTAGG[A/G]CATCTTTGAAATGTT | 7874 |
rs548730623 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8917918 | CCTCAGCCTCCCCAG[C/T]AGCTGGGACTACAGG | 7874 |
rs548760375 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892658 | CTGCCCCCGCAAAAC[A/G]GAATTAGAAGGAAAA | 7874 |
rs548766630 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8922381 | TAGTCCCAGCTACTT[G/T]AGACGCCGAGGCAGG | 7874 |
rs548766836 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8925536 | TCACCCTATACATTA[A/C]ATTTTCCAAGGTACT | 7874 |
rs548841488 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8918279 | CCCCACAACCAGGAG[G/T]GCCGATTTCCTGTAC | 7874 |
rs548875300 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8948906 | GAGCTTAAGGCTGCA[A/G]TGAGCTATGATCAAA | 7874 |
rs548902673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8947951 | TTCTCTGTCTCCAGG[A/G]TCTTTAGGCTCCATT | 7874 |
rs548951683 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8892239 | CGAACGGCTCTCGCA[C/T]CCCTGCTCTAACTCC | 7874 |
rs549015144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8935650 | GCAATTACCATCCCA[C/T]AATACGCATATCCCA | 7874 |
rs549036568 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8895264 | CCTATTTTTGCTAAA[-/C]AAAACGCCACACCTG | 7874 |
rs549051156 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8926888 | TCACTACCTTCCAAT[C/G]TGGCCCCTGGAGACT | 7874 |
rs549078239 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8958742 | GCAAGAATCATCAGA[A/C]GGCCACCAGGCTGAC | 7874 |
rs549088605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8931265 | GCAATCTCAGCTCAC[C/T]GCTACCTCTGCCTTT | 7874 |
rs549110026 | in-del | -/AT | | | intron-variant | USP7 | GRCh38.p7 | 16:8932836 | ATTTAAAGATGAAAA[-/AT]TTTTAAGAAGTAACA | 7874 |
rs549220654 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8955194 | ATTTAATAAACTTGG[C/G]TTTCTCTTTCCGTAT | 7874 |
rs549310597 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8936228 | GATCAAAACTACAGC[A/T]GTTATTACGGCAGAT | 7874 |
rs549311273 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8909489 | TACAGTCTGAAAGAT[A/T]AAAGGATTCTGTCTC | 7874 |
rs549339217 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8904884 | GGCTGAGGCAGGAGA[A/G]TGGCGAGAACCCGGG | 7874 |
rs549345669 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8940986 | GAATTCTCTCTCCTC[A/C]CACTCCAGGACCCTT | 7874 |
rs549397031 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8913649 | GCCGACCCGCACTAA[A/T]TGATTCCTAACGAGA | 7874 |
rs549402470 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8928439 | ATATGACAACCCTGA[C/G]ACATACGACAGTAAA | 7874 |
rs549408250 | in-del | -/C | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937206 | ACAGTGAGACTCTGT[-/C]TTTTTTTAAAAAAAA | 7874 |
rs549410425 | in-del | -/TCTGGAGAC | 0.00676609 | 0.0577691 | intron-variant | USP7 | GRCh38.p7 | 16:8908543 | CAAGATTGGAACATG[-/TCTGGAGAC]TCTGGAGACAAAGGC | 7874 |
rs549421411 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8953555 | CGTGCCCCATGCGGC[A/G]CCACCGGAAGCAGAG | 7874 |
rs549427322 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960789 | AAGTCACATTCCAAT[A/C]GTAAGGCTAGTACCA | 7874 |
rs549463464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8911556 | GCGCTGTCACGCTCC[A/G]GACACATGCGGTACA | 7874 |
rs549496329 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8943054 | GTGGACCCACTTTGA[C/T]GCTTTGCTCTATATG | 7874 |
rs549509388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960238 | GAAACATGCAACTGG[C/T]TGCTTCAGGCCTTAC | 7874 |
rs549512137 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938402 | CACATCTGTGGATTC[A/C]ACAAACCGCACATCA | 7874 |
rs549513049 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8904667 | TAATCTATTAGGCCG[A/G]CGTGGTGGCTTACGC | 7874 |
rs549635684 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8913497 | AGAAATGAGGCGAGC[A/G]AGAAGACGGTAGAAC | 7874 |
rs549640253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8923555 | ATTGCTTCCAATTTA[C/T]TAAAACCCGAAGACT | 7874 |
rs549660287 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8895350 | TTCTTCCCCCTCCCC[A/C]AAAAAACTGAATTTT | 7874 |
rs549668688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8955399 | ACAGGCATAAGCCAC[C/T]ATGCCCAGGCTCACA | 7874 |
rs549679022 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8928111 | AAATTCTATGTTAAC[A/C]GGATTTTTAAATAAG | 7874 |
rs549685797 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957276 | GCTTCCTCCAACTTT[C/T]TTAAGTCCAAATTAG | 7874 |
rs549693159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8913342 | GCCTGGGCAACAGAG[C/T]GAGACTCCCTCTCAA | 7874 |
rs549732339 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8947859 | CCTCCCTGCACAGCT[A/C]CCACTTTTGAGACCC | 7874 |
rs549755542 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8913363 | TCCCTCTCAAAAAGA[A/G]GAGAGAAGAGGGAAG | 7874 |
rs549763293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8953451 | TAAAGTCTGAGGTAC[A/G]ATCCAAGGGGAAACC | 7874 |
rs549796695 | snp | A/C | 0.133777 | 0.221342 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957773 | TAAATTAAAAAAAAA[A/C]CAAAAAAAAATTAAA | 7874 |
rs549832581 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8911986 | ATGTGGGGACAGGTT[A/T]TCCCTCAAGTAAAAC | 7874 |
rs549836030 | snp | A/G | 0.000550032 | 0.0165745 | intron-variant | USP7 | GRCh38.p7 | 16:8930266 | AAGTTTCCGCCCACT[A/G]CGAGGCGGTGAACCA | 7874 |
rs549893806 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8943509 | AGAGCCAAAGGATCA[A/G]CACCGAGAATGCAGG | 7874 |
rs550017619 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8948596 | ACAATCCTAAGAACC[A/T]GCACATCTCTTTGCT | 7874 |
rs550048984 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8906729 | TATGAAGTACATAAC[A/G]TAATCCGTACTTGAT | 7874 |
rs550070666 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962708 | ACGTAAGCCCGACGC[C/T]AGGCAGTGCTGTTAG | 7874 |
rs550079695 | in-del | -/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8933759 | CTGGCCTATACAAAC[-/T]TTTTTTTTTTTTTTG | 7874 |
rs550123771 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893220 | TCGTCTGTTCCACTT[C/T]AACGAAATTCTATTT | 7874 |
rs550147316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8912493 | ATAAACATTACCAAG[C/T]ATGCAAAGAAGCTGA | 7874 |
rs550154511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8926086 | GTGAACCCGGGAGGC[A/G]AAGCTTGCAGTGAGC | 7874 |
rs550196888 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960153 | ATAAATAATACACTG[A/C]CAAGCAACCTTATTC | 7874 |
rs550256665 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8951468 | GGAGCAGGGGGCTCA[A/C]CCACCTCGCCCTGAG | 7874 |
rs550272433 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8955693 | CCTGGCAACAGAGCA[C/T]GATTCCATCTCAAAA | 7874 |
rs550275255 | snp | A/G | 1.65685e-05 | 0.00287819 | intron-variant | USP7 | GRCh38.p7 | 16:8917159 | TCATGTACACAGCCT[A/G]AAACAATTAAGAAAT | 7874 |
rs550277608 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8921825 | AAGTGTGGGGTGGAC[A/C]ACAAAAGGGCCTCTA | 7874 |
rs550334986 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8944628 | AACCTAGCACAGAAA[G/T]AAAACTATTTTTTTC | 7874 |
rs550346711 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8900008 | TACAAAACAAAACCC[A/C]CTTAGGTAACAGCAC | 7874 |
rs550399465 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892426 | AAAGACCAGGAAACC[A/G]TGCCACGGAGCTGGA | 7874 |
rs550404922 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8926546 | GAAATTAGCTTTCAC[A/G]GATACGGCCAGCCAG | 7874 |
rs550430290 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8934481 | GGGTGGGGGAAATGC[A/G]TAAGCTCTACCCCCC | 7874 |
rs550462141 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8907912 | ACTCTAGCACATTCT[A/C]AAAGTTGACGCCAAC | 7874 |
rs550493232 | in-del | -/ACT | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8948138 | GGCCTGTAAAATCCC[-/ACT]AATAAATCCCTGCAT | 7874 |
rs550512878 | snp | A/C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8911577 | ATGCGGTACAGGACA[A/C/G]GGATCCCTGAAGGGA | 7874 |
rs550522259 | snp | C/T | 0.000884092 | 0.0210063 | intron-variant | USP7 | GRCh38.p7 | 16:8900634 | CGGTTTAACTTCCTA[C/T]AGTGAAAGATATAAA | 7874 |
rs550586060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8910593 | ATCCCCCTCTCCCTC[C/T]CCATTCAATTATCCT | 7874 |
rs550591106 | snp | A/C | 0.000199107 | 0.00997567 | intron-variant | USP7 | GRCh38.p7 | 16:8894652 | TAAACTAAAAGAAAA[A/C]AAATTAAAACTCCTC | 7874 |
rs550645357 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8896663 | GTATCCTTCCTCTGT[A/T]TGGCTTTTCTATGGG | 7874 |
rs550662437 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964787 | AGAATGAGACCCTGT[C/T]TCAACTAATAGTGAT | 7874 |
rs550682682 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8918613 | TCAGGAGTTCGAGAC[C/G]AGCCTGGACAACATG | 7874 |
rs550711896 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8933264 | GTTAAAAAAATTTAG[C/G]CAAGCACAGTGGCTC | 7874 |
rs550729609 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8923488 | TAATCGACATGGAGT[A/C]AACTGTTCTATACAT | 7874 |
rs550749403 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8944990 | GGCGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 7874 |
rs550762078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8914269 | ATCTTTCAAAGTCTG[A/G]CAACTGACAGCTCCA | 7874 |
rs550765408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8924730 | TTTCTGACTGAGTTT[A/G]GTCTTAAGAAAACAT | 7874 |
rs550804234 | in-del | -/A | 0.00636936 | 0.0560724 | intron-variant | USP7 | GRCh38.p7 | 16:8895754 | GCCTGAACAGAGAGG[-/A]AAAAAAAAATAGGGC | 7874 |
rs550848758 | in-del | -/TGC | | | utr-variant-3-prime, nc-transcript-variant, cds-indel | USP7 | GRCh38.p7 | 16:8893900 | AGCAGCGAATCCTCT[-/TGC]TGAAGACTTCGGCTA | 7874 |
rs550851684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8942274 | GACACTCGGAGTGAC[C/T]GGGATGCCCAGTGGA | 7874 |
rs550873117 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891962 | GAGGCCGGAGAAGGG[A/G]AGTTCATTTTTCTTT | 7874 |
rs550909141 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8900005 | CACTACAAAACAAAA[C/T]CCCCTTAGGTAACAG | 7874 |
rs550939923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8941821 | CTCCGTCTCTGACAG[A/G]TGGGCTGGGCCCAGG | 7874 |
rs550966863 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8905697 | CTGAGCACACCAAAC[G/T]AGAGTTCAAATTTTA | 7874 |
rs550968979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8933044 | CTCCGGGGTGCCAGC[A/G]ATTCTCCTGCCTCCA | 7874 |
rs551003445 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8911100 | TTCGAACAAAGCACA[A/C/T]ACTGTAAAGCTATGA | 7874 |
rs551006544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8912798 | TACATAGAAAAAAAA[A/G]AAGAGATAAAGATTT | 7874 |
rs551006877 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8907294 | AAACATACCAACAGG[A/T]TGGAATTGGTCTGAA | 7874 |
rs551048989 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8902969 | TTATCCTTCAGGATC[A/G]AATGCCCATTTACAA | 7874 |
rs551094626 | in-del | -/GGACACTACA | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8953395 | TACACCAGCCTCTGT[-/GGACACTACA]GGACACCAAGGACAC | 7874 |
rs551132306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8896403 | AGGGTCTCACTGTTT[A/G]ATAATTGTTTTATTA | 7874 |
rs551176728 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8918874 | CAAAGTAGGTGTCCC[A/G]GCACTGGGGAATGAA | 7874 |
rs551183184 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8926430 | GTTGCACTGAGCTGA[C/G]ATCATGGCATTGCAC | 7874 |
rs551188544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961981 | AGCCACTTTGTCATT[C/T]GCAACCTGGCCAGCC | 7874 |
rs551195546 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8952434 | GAAATGGGTCTCACC[A/G]GGCTAAAACCAAGGT | 7874 |
rs551293495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8926795 | TACCGCATGCTTCTT[C/T]TTACTGTAAATGACA | 7874 |
rs551308092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8952756 | ATTCTGCAAACCACA[A/G]ACCCTAAACCTCTAG | 7874 |
rs551308599 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8931210 | TTTTTTTTTTCTGAG[A/T]CAGAGTCTCGCTCTG | 7874 |
rs551344206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8945061 | GTTCAAGACCAGCCT[A/G]ACCAAGATGATGAAA | 7874 |
rs551357270 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962934 | GCTGCCTGAGCGCTC[G/T]AATTTACAACTCAGG | 7874 |
rs551392440 | in-del | -/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8920994 | AAAGCTGCTAAAAAC[-/G]TAAGATACGAAACTG | 7874 |
rs551394207 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8935845 | CCAGCTTTCCTCCCC[A/G]TGAATTCCATTTGTG | 7874 |
rs551409135 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8899275 | ACTTAAAATGTGCCA[C/T]GAGCAGCCTGAATTT | 7874 |
rs551418171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8940893 | AACCTGGAATATATA[C/T]AGTCTCCAGAACCTG | 7874 |
rs551430295 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957119 | TCCAAATAAAAAGTT[A/T]AAATTACCAACCCTC | 7874 |
rs551499177 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8935352 | GTAGCTGGGATTACA[A/G]GCACCTGCCATCATG | 7874 |
rs551526193 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964139 | CCCCGGGCCCTGGGG[G/T]CCGAGGCGGGCCGCC | 7874 |
rs551571126 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8913586 | TCTTTCACAACTGCA[C/G]ATGAAATAAAATCTT | 7874 |
rs551580972 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893838 | AGGGCAGTCAATAGA[A/T]ACAGAGAAGCCAAAC | 7874 |
rs551594401 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8898139 | AAGGGAAGGGTTGGC[C/T]GCCGAATGGTTCCTT | 7874 |
rs551627650 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8945323 | TGGGAGGTGGAGGTT[A/G]CAGTGAGCCAAGACC | 7874 |
rs551638708 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8958490 | TAAAGTGTGGGGTCA[C/G]GCAGGCTGGAAGCAG | 7874 |
rs551677498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8959478 | GAGCTGGAGCCTGGG[A/G]AATCGCTTTGAATCA | 7874 |
rs551700295 | snp | C/G | 0.000114136 | 0.00755346 | intron-variant | USP7 | GRCh38.p7 | 16:8936573 | AGCTCAACCTGAAAA[C/G]CTGACTCACCTTCCA | 7874 |
rs551708772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8954514 | ATTACCCTGTTAACC[A/G]TAACTCAAAAAGTCA | 7874 |
rs551720106 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892356 | TCAGAGCAGAAGGCA[C/G]ACACACTGCAGTGGA | 7874 |
rs551747450 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8946750 | CAGCCACTCACGCTC[A/C]ACCACTCAGCCATCT | 7874 |
rs551788384 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8928246 | TCAAGTCGCTGATAG[C/T]TTGGCTACAGACCAA | 7874 |
rs551821368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8943031 | GCAGTGGAGCCTGAG[C/T]GTTCAAAGTGGACCC | 7874 |
rs551857166 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8913689 | CAAATTAAAAACGGA[G/T]GAGCATTGCAAGCTG | 7874 |
rs551858285 | snp | C/T | 2.00717e-05 | 0.00316787 | intron-variant | USP7 | GRCh38.p7 | 16:8915576 | TTGTACTTAGTAATA[C/T]ATACAGTAATTTTAT | 7874 |
rs551890617 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8908847 | GAAAACTCTGGTTAC[A/C]ATTACCCAAGATTAG | 7874 |
rs551909933 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8965470 | GAATCACTTGAACCC[A/G]GGAGGTGGAGGGTGC | 7874 |
rs551915760 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8952249 | GGAGAGCCTGTCTCC[A/C]AAAAAATATTAATTA | 7874 |
rs551928456 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8914696 | CCCAAGGCAGGAAGG[C/G/T]TGCTTAAACCCAGGA | 7874 |
rs551964329 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8904632 | TAGAAGCTCCCGATT[A/C]TAGGTCATCATTAAT | 7874 |
rs552053414 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8899387 | GATAACTTTGGAAAG[C/G]GTTTTCACTTTTAAT | 7874 |
rs552066782 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938349 | ACAGTCAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 7874 |
rs552073457 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893316 | CTTAATTGAATTTAA[C/T]AATGTTCTTGATTTA | 7874 |
rs552123410 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP7 | GRCh38.p7 | 16:8920163 | ACAATTATGTTCCAA[A/G]GGTCTAACATATAGA | 7874 |
rs552123826 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8904798 | AAAAAAAAAATAAAA[A/T]AAAAATAAAATAAAA | 7874 |
rs552135251 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893224 | CTGTTCCACTTTAAC[A/G]AAATTCTATTTATAA | 7874 |
rs552143568 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8952654 | TCCTGAATTCAATAA[C/G]GTCTGCAAAATCCCT | 7874 |
rs552149472 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957143 | AACCCTCAGAAGTAG[A/T]CCTGCTTCTCTTCAA | 7874 |
rs552188185 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962398 | CGTCTTCACATCCAA[A/C]CTTTACAACCAAGAC | 7874 |
rs552208128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8901787 | GTCCCTGACAGACAA[C/T]GTTTGCAACCCTGCT | 7874 |
rs552268018 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957566 | CTGAACATAGCAAGA[A/C]CCCATCTCTACAAAA | 7874 |
rs552283496 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8896384 | TCTTATTAGGTAATA[A/G]ATTAGGGTCTCACTG | 7874 |
rs552330904 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8896612 | CAAAATCAGGAGTCA[A/C]CCCTTCCAGTTTCAG | 7874 |
rs552358160 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8906158 | CACGAGCATTCAGAA[A/G]AAAATATAAGTGTCT | 7874 |
rs552361205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8948070 | TGCATGCCCTGCAGA[C/T]GTCAGTCAGCTCCAG | 7874 |
rs552407729 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8934303 | GGTACAGGTTATGGT[A/T]TCATGAGATGCAGTG | 7874 |
rs552447120 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8911536 | ACTGCACAACACTGA[A/G]AACAGCGCTGTCACG | 7874 |
rs552459384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8929589 | ATGGACATGCTTTTT[A/G]ACAGAACATGGTTTC | 7874 |
rs552485565 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938697 | GCTTGGGTAACACAG[C/G]AAGACTCCGTCTCAA | 7874 |
rs552508816 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8916726 | TAGATTTACTGCTGG[G/T]GAAGTGGTGTTTCCA | 7874 |
rs552572086 | snp | C/T | 1.99011e-05 | 0.00315439 | intron-variant | USP7 | GRCh38.p7 | 16:8902506 | AATATTAAGAGTAGA[C/T]TAAAATAAAAACACG | 7874 |
rs552593523 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950614 | CGCTGACAGAGACAA[A/C]AGTCTCAGTTACCAA | 7874 |
rs552623241 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8925168 | GAAATGGAGGTTCGC[A/C]GAGGCTGTTTTACAA | 7874 |
rs552645046 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8913153 | CTGAGGTCAGGAACT[A/C]GAGACCAGCCTGCCC | 7874 |
rs552649431 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8954616 | CTACAGAGATGAAGA[C/G]TTGCCAAAAACTTTA | 7874 |
rs552672189 | in-del | -/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8919619 | TTTTTTATTTTGTGA[-/T]TTTGGTGGTTGTTTG | 7874 |
rs552703161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8926027 | GGTGCAGAGGCTGGC[A/G]CCTGTAGTCCCAGCT | 7874 |
rs552749321 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8921379 | TAAACATAGCACACC[A/G]AAATTCCCATTTATG | 7874 |
rs552788354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8917939 | GGACTACAGGTGCAC[A/G]CCGCCATGCCCAGAT | 7874 |
rs552818059 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8931645 | AGTTCGGATTCAAAA[C/T]ATTTTAAGTTACCAC | 7874 |
rs552909529 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8943979 | AAAGCAAAACTATAA[C/G]GTGCGGGGGAGGCAG | 7874 |
rs552962454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8936229 | ATCAAAACTACAGCT[A/G]TTATTACGGCAGATA | 7874 |
rs552973706 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8954278 | GGAAGCAGAGGCTTT[C/G]AACAGGTGCCCCTGG | 7874 |
rs553060373 | snp | A/G | 1.64844e-05 | 0.00287087 | intron-variant | USP7 | GRCh38.p7 | 16:8899803 | TCAAAGTCCATGGCA[A/G]GGGGTAGCTGGTAAA | 7874 |
rs553063578 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8917639 | CCACCTTGGCCTCCC[A/G]AAGTGCTGGGATTAT | 7874 |
rs553094784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8927665 | ACATGGTGAAACCTC[A/G]TCTCTACTAAAAATA | 7874 |
rs553124912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8940619 | CACAGAAACAGGGAC[A/G]ATGGTGGCAGCCAAA | 7874 |
rs553182651 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8904037 | CGTGCACTTAATCAC[C/T]TCTCTGTCTGGTGGC | 7874 |
rs553201802 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8900103 | AGCCCAGTCTCTGAC[C/T]GTGAGTCAGGAAATC | 7874 |
rs553216480 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8904348 | GACCTGGGAGTCCCA[C/G]AGGGGTGGGGGCTGA | 7874 |
rs553221270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8941661 | CTTGGTACCAGGAAA[A/G]ACAAAGACCAGGCCG | 7874 |
rs553239460 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8935891 | ACTGCTACCCCACCA[A/G]AGAACACCTCCCAAT | 7874 |
rs553287932 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8965127 | CTTCTCTCCATCTCC[C/G]TATACCCGCTTTCCC | 7874 |
rs553294828 | snp | A/G | | | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962462 | ACTGCCACATCGGCA[A/G]AAAACCGAGTTACCT | 7874 |
rs553309946 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8923661 | GCCATCCCTGTCAGA[A/C]TGAGTTCCACATGAG | 7874 |
rs553325974 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | USP7 | GRCh38.p7 | 16:8955480 | GTAATCCCAGCACTT[G/T]GGGAGGCCGAGTGAG | 7874 |
rs553420859 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8918873 | ACAAAGTAGGTGTCC[A/C]AGCACTGGGGAATGA | 7874 |
rs553532539 | in-del | -/AC | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8910398 | AGAAACACAACCTAA[-/AC]ACAGTCCAACTTACT | 7874 |
rs553563702 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956845 | AGAGCCCAGCCCCCC[C/T]GCAGGCAGTGCCCCA | 7874 |
rs553620441 | in-del | -/TT | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8900382 | CACCTAATTTCAAAA[-/TT]CCCAGAGAAAGCCTC | 7874 |
rs553624216 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | USP7 | GRCh38.p7 | 16:8959159 | CTTGACGGGCATGAA[C/T]GACCTCCTTTAAGGG | 7874 |
rs553661083 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | USP7 | GRCh38.p7 | 16:8948048 | CCACCCACCACCTCT[A/C]GAAGACTGCATGCCC | 7874 |
rs553669402 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8948201 | AACCCTCAACTGACC[C/T]TGATTCCTCCCTCCC | 7874 |
rs553684151 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8902004 | GGGAAGAAGGCTTAA[C/G]CCTGTGTGTTTAGAA | 7874 |
rs553701392 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8914394 | CTGGACATACGCACA[A/C]CCTACAGGCCAGTAA | 7874 |
rs553707923 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8920602 | TTAGACTGTTTCAAT[G/T]TTCTTTTAACAGTGG | 7874 |
rs553728127 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892452 | CTGGAAGGCAAGGCC[A/G]ATGGGACGGTGCAAG | 7874 |
rs553742844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8944187 | TTTCCGGGAATATGC[A/G]TTACTCTTAAAACAA | 7874 |
rs553774130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8906324 | ACATAGATCAGTTAG[A/G]GGTCCCTGACAAGGT | 7874 |
rs553777969 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8943684 | AGTCGAATGGCTGGC[A/G]GGAACACACTTTTCT | 7874 |
rs553802541 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8917445 | GTGCAGTGGCGCGAC[A/C]TCAGCTCACTACAAC | 7874 |
rs553846278 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8901468 | CATGGAAACCCACTA[C/T]ATTTAGACAGTCAAG | 7874 |
rs553850663 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8907039 | GTTGCAAAATTAACA[C/G]AGGCAGGAAGGCAAG | 7874 |
rs553871548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8939133 | TTTACATGTACTTAC[A/G]TGTATTTAGTTCTCT | 7874 |
rs553878758 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962521 | CAGCCATGTGCGGCA[A/C/G]GGCTTTCGCACGGTT | 7874 |
rs553911840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8896685 | TTCTATGGGAACTGC[A/G]CCTTTTTACTACAGC | 7874 |
rs553912288 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964271 | CACCCGGCAGCCGGG[A/G]TTCAGGTCCCAGCCT | 7874 |
rs553955041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8925722 | AGTGCACTGCACACT[C/T]GATTTCAGCCTCACA | 7874 |
rs553972547 | in-del | -/T | 0.00993419 | 0.0697739 | intron-variant | USP7 | GRCh38.p7 | 16:8896829 | GAGCAACACTGGGTC[-/T]TGTGTTGAGCTTCTG | 7874 |
rs553993437 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8892833 | CAAAAAGGCAATATA[C/T]AGGAAGAGTTGGTGT | 7874 |
rs553993733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8963039 | CTCGCCCGCGGACCC[A/G]GCATGACTTTGCAGC | 7874 |
rs554033681 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8958015 | AGAGCCACTTGCCAG[C/T]CAGCCATCTCCTGCA | 7874 |
rs554049102 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893570 | AAGGTCATTGAAAGT[A/G]TAACTGAAGGAAATA | 7874 |
rs554051121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8898255 | TCATGTGCTGTTGTT[C/T]AGAGTGTTTTTCTGT | 7874 |
rs554056492 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8935431 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG | 7874 |
rs554070226 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8921034 | TGTTTTCAAAGACAC[G/T]TGTCCAATTTAGAAA | 7874 |
rs554132759 | in-del | -/TG | | | intron-variant | USP7 | GRCh38.p7 | 16:8902897 | AAAAGAAAAAAAGAC[-/TG]TGATTCTAAGAAAAA | 7874 |
rs554136712 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8930796 | CAACATGGTGAAACC[A/C]CGTCTCTACTAGAAA | 7874 |
rs554171577 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950826 | GACAGTGATCTGAGC[A/G]GGCACTATTTGTCAC | 7874 |
rs554211107 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8935013 | AAGAAATCTGTACTA[C/G]ACTTCTAGAAATAGC | 7874 |
rs554215712 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | USP7 | GRCh38.p7 | 16:8952076 | TAAATAAAAAAGTAG[-/A]CCCCCCCGTCTATAC | 7874 |
rs554217710 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8912203 | ACGCCTGTAATCCCA[C/G]CACTTTGGGAGGCAG | 7874 |
rs554221509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8907468 | ATTCCATACAAAGCT[A/G]GTGCTCAAACTAATC | 7874 |
rs554264614 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8946004 | GGACAGGGGAGAATG[A/G]AAGAGTCCAGAAACA | 7874 |
rs554281394 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8912483 | AAAAAAGAAAATAAA[C/T]ATTACCAAGCATGCA | 7874 |
rs554350677 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8947405 | CCAGGCCGAAGTACA[G/T]TGGTGCCATCTCGGC | 7874 |
rs554383267 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8927815 | TACTCTAGCCTGGGC[A/G]ACACAACAAGAACCT | 7874 |
rs554389664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8930739 | TTTGAGAGGCCAAGG[C/T]GGACAGATCACCTGA | 7874 |
rs554417438 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8903069 | AAAATCCTGTGGGTT[A/C]CCCTGTGCAGGAGTC | 7874 |
rs554461751 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8962044 | AAGTTATTCTATTCA[C/G]AGGTGAACACCAGTC | 7874 |
rs554467279 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8926589 | CGAGGAATTACATGA[C/G]ACTCAGTGATGGAGA | 7874 |
rs554517847 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8909693 | AGCACTTTGGGAGGC[C/T]GAGGCAGGCGGATCA | 7874 |
rs554543494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961112 | AATATGAAAATAAAG[C/T]TTCATTTTATGAGAA | 7874 |
rs554550799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8926251 | GGGAGGCAGAGGCGG[A/G]CGGATAACCTGAGGT | 7874 |
rs554553128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8931020 | TACTTTACAATAGCT[A/G]ATCAGCGTAAAGAAC | 7874 |
rs554574954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8945591 | AGACTGGGGACATAC[C/T]GTGCCCATGGAGTGG | 7874 |
rs554590674 | snp | A/G | 0.000281455 | 0.0118595 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8895711 | TTCTTGATGAACACC[A/G]ATGATTTTGTAGCTT | 7874 |
rs554649056 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891739 | AGCACGAGCCACCGC[A/G]CCTGGCTGCTCTTCT | 7874 |
rs554703818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8905431 | GTGAACTTCTAGGTA[C/T]GCCCCTAGTTGAAAA | 7874 |
rs554718513 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962833 | GGAATTCCCCAGCCA[A/C]ACCAGATCCAACCGG | 7874 |
rs554724332 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937294 | TCACGCCTGTAATCC[C/G]AACACTTTGGGAGGC | 7874 |
rs554746127 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8915734 | ACAGTTGAGGTTAAC[C/G]TTTTATACAGCCTTT | 7874 |
rs554764410 | in-del | -/ATAAC | | | intron-variant | USP7 | GRCh38.p7 | 16:8907990 | AAAGTCCCCTCTGAA[-/ATAAC]ATTTATAATCGGTCA | 7874 |
rs554805483 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8925791 | CAAGCACAAAGTTTA[C/G]ATGACACTTCGGGTG | 7874 |
rs554813817 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8933672 | TGCCCAGGTTGGTCT[G/T]GAACTGGACTCAAGC | 7874 |
rs554821661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8911648 | TTACAGGCTGCAGCC[C/T]GGAGAAGGCAAACCC | 7874 |
rs554831104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8911398 | CCCTAAAATTAAGAA[C/T]GGTAACATTAAGAGT | 7874 |
rs554889617 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8949759 | GCTTTCCTTACGCAG[A/T]GACACCTTATCACTT | 7874 |
rs554905683 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | USP7 | GRCh38.p7 | 16:8956318 | ACCACCTTGAGAATG[C/G]GCCACAGCGCTCGCT | 7874 |
rs554928196 | snp | A/C | 0.046775 | 0.145601 | intron-variant | USP7 | GRCh38.p7 | 16:8904697 | CCTGTAATCCCAGCA[A/C]TTTGGGAGGCTGAGG | 7874 |
rs554945193 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8905939 | TCCCCTTGGCAGGAG[C/T]TCGGTGCTGGCCCTG | 7874 |
rs554953059 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8933112 | CGCTTGGCTAATTTT[C/G]TATTTTTAGTAGAGA | 7874 |
rs554966052 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937936 | ACCACGTGAGAAGGA[A/G]CTACCATCTGCTTAA | 7874 |
rs554992619 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8897649 | AGAAGGATGCTTGAG[C/T]CCAGGAGCTCAAGAC | 7874 |
rs555016455 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8958572 | GCTTTCAGGGGATGT[A/C]TGAGACAGCCAAACG | 7874 |
rs555037436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8919948 | CTCCTCGCTCACCAT[A/G]TTAGTTGTCGGTGAT | 7874 |
rs555037810 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8917356 | GGGATACTGGAAAAC[A/C]TAAGAATGCAAAAAT | 7874 |
rs555068652 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, nc-transcript-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8892044 | CTGACACTGTAACTG[C/T]GAGTGAGTGGAAAAG | 7874 |
rs555071387 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8943628 | AACGGTGAAAAGCAA[C/T]GGAGATGCCCACCAG | 7874 |
rs555109961 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | USP7 | GRCh38.p7 | 16:8929132 | TCCGATAGGGCAGGG[A/C]CTGTCACTGCTACAC | 7874 |
rs555114085 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8952508 | TTTCCCTGCCGCTTC[C/T]GGGTCCTAGAGCCAC | 7874 |
rs555121650 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8945611 | CCATGGAGTGGGAGA[A/C]AGCACAGTAAAGATG | 7874 |
rs555147523 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8917597 | TTGGCCAGACTGGAC[C/T]GAAACTCCTGACCTC | 7874 |
rs555194723 | snp | A/G | 0.000115406 | 0.00759537 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893952 | TTCTAGGCTGTTAAG[A/G]GGCCACCCACACACC | 7874 |
rs555196909 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8926503 | AAATTCAAGATAGGA[C/G]GGCCAAAAAAAAGGA | 7874 |
rs555209521 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938442 | AGGGGGCCGGGCACG[A/G]TGGCTTACACCTGTA | 7874 |
rs555216884 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8935513 | ACCATGCCCAGGCTA[A/T]GGCACTATTTTTGAC | 7874 |
rs555248077 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937398 | AATACAAAAATTAGC[C/T]AGACGTGGTGGCGCA | 7874 |
rs555286781 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8954804 | CTCTACTAAAGATAC[-/A]AAAAAAATTAGCCGG | 7874 |
rs555317416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8935827 | GGCACTTAATGCCTA[C/T]ACCCAGCTTTCCTCC | 7874 |
rs555330122 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893477 | AACCCGAGGAAGGGC[A/C]GACAATGCACACAAT | 7874 |
rs555354763 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8926243 | AGCACTTTGGGAGGC[A/C]GAGGCGGGCGGATAA | 7874 |
rs555386197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8945098 | CTGTACTAAATAAAA[A/G]TACAGAAATTAGCTG | 7874 |
rs555392840 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8932012 | GCCTTTCTGCCATCC[A/G]AACCAGCAAGCAATC | 7874 |
rs555441917 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961001 | CTTAAGTTTAAGGAA[G/T]CAGCATTAGTAACTA | 7874 |
rs555479459 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8931513 | ACCCTCAAGGTGTCA[A/G]TGGACAATTCCTGTA | 7874 |
rs555516864 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8948742 | CAAGCATGGACAACA[C/T]AACGATAAAAGCAGC | 7874 |
rs555526185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8944836 | GGCGGCTGGACACAG[C/T]GGCTCATGCCTGTGA | 7874 |
rs555541984 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8932885 | GAATATATTTATGTA[C/T]TAACTGAATAGGAAA | 7874 |
rs555578237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8954698 | CAGCAATTGCAGGCC[A/G]GGCACGGTGGACTCA | 7874 |
rs555626820 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8949091 | CTCGAATTGAATGCT[C/G]ATAGTCACACAATTG | 7874 |
rs555636099 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8940111 | TCCAAAAAAAAAAGG[C/G]TGTTTCCATCCAGGT | 7874 |
rs555636490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8916716 | AATTCAAAGATAGAT[C/T]TACTGCTGGGGAAGT | 7874 |
rs555660848 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8951488 | CTCGCCCTGAGCCAG[-/C]CGGATTCATGTGATG | 7874 |
rs555750896 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8904295 | GAGTGGGGACTGACC[A/T]GCACTTGCGTACAGA | 7874 |
rs555783907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8927118 | AGGTCAGGAGTGCGA[A/G]ACCAGCAGCCTGGCC | 7874 |
rs555797682 | in-del | -/AAT | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8898309 | GGGACAGGTAGAAAC[-/AAT]AAGCAAGTTCCAATA | 7874 |
rs555812426 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8959052 | GCAAAAGCCCTACCA[C/T]CAAGGCAACACCATG | 7874 |
rs555838834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8903665 | TGAGGTCAGGAGTTC[C/T]GAGACCAGCCTGACC | 7874 |
rs555908361 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8910124 | GAGTCAATGAGTCAA[C/G]GTTATAAGATTACAA | 7874 |
rs555942108 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8922456 | TCAGGCCACTGCACT[C/T]CAGCCTGGCGACAGA | 7874 |
rs555974708 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | USP7 | GRCh38.p7 | 16:8894446 | GTCGGCCAGTGGAGA[C/G]AGAGGAGCTGGCACT | 7874 |
rs555981361 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956546 | GAGGCGGGCAGACTG[C/T]CTGAGCTCAGGAGGT | 7874 |
rs556042366 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8912310 | TGCAAAAATTAGCTG[A/G]GTGTGGTGGTGGGCA | 7874 |
rs556044900 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8899570 | TGTCTTTCTGGAGTG[C/G]GATCTGAAGAGGAAA | 7874 |
rs556060572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8952871 | GGAGTCTCATTCTTG[C/T]TGTCGCCCAGGCTAG | 7874 |
rs556074121 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8912421 | CATGACTGCACTCCA[A/G]CCGGGGCGACAGAGT | 7874 |
rs556087872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8918442 | ATAAAACTTTGCAAA[C/T]GTTGCTGTTAATGGA | 7874 |
rs556133660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8896092 | GATCCGCCCGCCTCG[A/G]CCTCCCGAAGTGCTG | 7874 |
rs556147258 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8905879 | AACGCTGCTGTTACA[C/T]GCACTCTTCACTGTT | 7874 |
rs556163294 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8911271 | TGGAAGTTGGTCCTG[A/C]CATCTCCCCACCCCC | 7874 |
rs556174753 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8953078 | CTGACCTCGTAATCT[C/G]TCGCCTTGGCCTCCC | 7874 |
rs556233155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8905517 | AGCGCCTCAGGCATC[C/T]GCTCATACAATTCAC | 7874 |
rs556274007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8952855 | TTTTTTTTTTTAAGA[C/T]GGAGTCTCATTCTTG | 7874 |
rs556282729 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8943408 | CAATGCAAGTAGAAG[G/T]TGCAGCACGCACGGC | 7874 |
rs556291416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8902757 | GCTGGGCCTGGTGAC[A/G]GGTGCCTGTAATCCC | 7874 |
rs556312725 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8939285 | TGCTCCCCCATTATC[C/T]CCGGCAACCCTCATA | 7874 |
rs556341252 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8929785 | ACATATGAGTATGCT[G/T]TCTCACAGAGAAGCT | 7874 |
rs556374158 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8913576 | AGTTAAAATGTCTTT[A/C]ACAACTGCAGATGAA | 7874 |
rs556407785 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8924935 | CTTGTCCAAAATAAT[A/T]ATTTATTTGAGCCTC | 7874 |
rs556446813 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8901891 | GGCTGCTACTGTCTC[A/C/T]GGGCCTCACAGGAAA | 7874 |
rs556449228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962630 | AAACCAACAGCGCCC[A/G]GGTCAGAACTCTGGG | 7874 |
rs556450148 | snp | C/T | 1.64784e-05 | 0.00287035 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8897082 | ACACCCATGCTTGTC[C/T]GGATATAGTGTTATT | 7874 |
rs556451810 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8925197 | AAAGTGACAATAGAG[G/T]ATTTTAATATCCAAG | 7874 |
rs556519078 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8948173 | CTTTCCCACAGTTCC[C/G]CTCCCCTGATGGAAC | 7874 |
rs556570778 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8954942 | TCCACCCTGACAACA[C/G]AGCGAGACTCCATCT | 7874 |
rs556583470 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8947827 | ATGCTGCCTCAGCTA[A/G]GTGGGCATGCCATGC | 7874 |
rs556596836 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8912115 | TAACACCCAGCAAGA[G/T]AAAAACCACCATGCC | 7874 |
rs556598018 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8916396 | CTGATCCTAAACAAA[C/G]ATGGGCATTTTCTGA | 7874 |
rs556601711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8920998 | CTGCTAAAAACGTAA[A/G]ATACGAAACTGGAGA | 7874 |
rs556612499 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950092 | TTATTAATCTTATTC[A/C]ATTTAATTTTATTTA | 7874 |
rs556622554 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8930465 | AATAAGCAAAATATA[A/C]ACTTATACTTTTGAT | 7874 |
rs556628474 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8909087 | GGACTCTGTGGGACA[G/T]GACACCCCAACTTCT | 7874 |
rs556629874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8943645 | GAGATGCCCACCAGT[A/G]CTGAAGGTCTAGCAT | 7874 |
rs556649212 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8918403 | TAAAAGTAAGTTGCA[C/T]TGACTTTTCAACTCA | 7874 |
rs556668920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8939124 | TTCTCCACATTTACA[C/T]GTACTTACGTGTATT | 7874 |
rs556669603 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8939951 | AAAAATACAAAAATT[A/G]GCCAAGCATGGTGGC | 7874 |
rs556681919 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950188 | TGTATTTAATTTAAT[C/T]AACCACATGTGGCTA | 7874 |
rs556703733 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8931088 | GTTTCCTAGTAATTA[A/C]AACAATTCTACAGCC | 7874 |
rs556712767 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8910002 | CAGAAGAGTACATTT[C/G]GAGCTGACAGCTGAC | 7874 |
rs556756580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8906985 | AGTTTTAACTGGCTC[C/T]ACAAATTTTGATTTA | 7874 |
rs556781287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8939492 | GCTGCTATGAAAATA[C/T]TGGACTGGTCCTGGT | 7874 |
rs556788107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8945535 | TCTGTGCACTAGTGA[C/T]GTACTGTGAATGCTA | 7874 |
rs556795179 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8963025 | CCCGGCGGCCGCCCC[G/T]CGCCCGCGGACCCGG | 7874 |
rs556825327 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8904985 | AAAAAAATAAAATAA[A/T]ATAATCTATTAACAT | 7874 |
rs556881007 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8913505 | GGCGAGCAAGAAGAC[A/G]GTAGAACGTCTAACA | 7874 |
rs556901616 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960219 | TCTATCTGCCTTCCA[A/T]CTAGAAACATGCAAC | 7874 |
rs556931133 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8932588 | AACTAGCTCAAATGC[G/T]CCAAATCAAATATAC | 7874 |
rs557035647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8895244 | ACTCTAACCCGGAGG[A/G]TAAAGCCTATTTTTG | 7874 |
rs557064911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8941152 | CCCATGAGGACCCCC[C/T]GCCCCACCACCAAAT | 7874 |
rs557094077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8928243 | CAGTCAAGTCGCTGA[C/T]AGTTTGGCTACAGAC | 7874 |
rs557103878 | in-del | -/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8919386 | GGCACTCCTGTCACT[-/G]ATCAAGCCCAGCACC | 7874 |
rs557175602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8941558 | CACATTTCGGCTTTT[C/T]TGTCCACGCACGATA | 7874 |
rs557209222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8899892 | AGGTTCCCCTTTGAG[A/G]GGGCCAGGCATCTGC | 7874 |
rs557237480 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8915084 | TGCTGGCCAACACCA[C/G]AGCTGGGTGGAGGTA | 7874 |
rs557242209 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8941995 | GAAGGAGGAGACAAC[C/T]GGCAAGCACAGAGTG | 7874 |
rs557348360 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8910891 | TGTAGCCAACACAGG[G/T]GTAAGTTATTTAAAT | 7874 |
rs557351197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8955562 | ATACAAAAAATTAGC[C/T]GGGCATGGCGGCGCG | 7874 |
rs557385235 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8949832 | TTACCAGCAAGTATG[-/C]CCCTAAGCTGAGCTT | 7874 |
rs557417078 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8958074 | AAAAGTGTTTCCTGA[A/G]TGAGCATCTCCCACA | 7874 |
rs557444294 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892707 | TTGTTACAAATGCCA[A/G]GGTTTCCCAGGCCTG | 7874 |
rs557452170 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8951273 | CTTTAAAATCTGGCC[G/T]CTTAAGTCACCTAAT | 7874 |
rs557510279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8955961 | GAGAGACAGCCAGAT[A/G]TCAGATTACCACCCA | 7874 |
rs557544995 | in-del | -/A | 0.000500988 | 0.0158191 | intron-variant | USP7 | GRCh38.p7 | 16:8923418 | CCAACTGGTGTCTGC[-/A]AAAAAAACACATCAT | 7874 |
rs557571750 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8897508 | GTGAGGCTATTTATG[A/T]CTCGAATTTTCCCTC | 7874 |
rs557602096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8939775 | AATAACTCCAAAACA[C/T]TGTCATGATTTATCA | 7874 |
rs557602364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8944770 | ACCTGCAATTCAAGG[A/G]CTGTCAGATCTTTTG | 7874 |
rs557625996 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891721 | CCCTTGGGCTTTGCT[C/T]ACAGCACGAGCCACC | 7874 |
rs557698779 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8892990 | AAACGGGGCTGGGAC[C/T]GAAATAAAACTACAC | 7874 |
rs557700682 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8948366 | TTTTGGCATTTTTTT[G/T]TAGAGACGAGTTTTC | 7874 |
rs557701280 | snp | A/T | 8.23839e-05 | 0.00641757 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8897016 | AAGTTTCCCTGATGC[A/T]TTCTCCCCAAGCTCC | 7874 |
rs557714467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8940030 | TTGAACCAGGGAGGC[A/G]AAGGTTGTAGTGAGC | 7874 |
rs557748681 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957387 | AACTCTTGTTCTCCA[A/G]GATAAAACTTCTTTG | 7874 |
rs557766460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8917526 | TGGAATTACAGGCAC[A/G]CACCACCACGCCAGG | 7874 |
rs557832417 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962567 | GCCGGATGCTGGCTG[C/G]ACCACACACTGCCAA | 7874 |
rs557846337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8935117 | CATGTAAGAGTGATG[C/T]AATACCAAGTTTTAT | 7874 |
rs557855327 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937864 | TGCTCAGGAGACCTG[C/T]AGCCAGTCTGGGGAG | 7874 |
rs557857240 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957751 | AACAGAGCAAGACCC[C/T]GTCTCTTAAATTAAA | 7874 |
rs557877034 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8913031 | GCCAGAATCAAACAA[A/C]TGAAAACCAGTGAGA | 7874 |
rs557892301 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8954381 | GTGTTCAGTGGGCTC[C/G]CTCATCTCTCTAAAC | 7874 |
rs557894017 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8939750 | CTATTCACATTACGT[A/G]GGTAAGTTTAATAAC | 7874 |
rs557941278 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8912069 | CTTACAAGTCACTTA[C/T]CTGTGCATAAGAGCA | 7874 |
rs558025378 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893359 | CCACAATGTCTGTCC[A/G]GACTGTATTCAGTGC | 7874 |
rs558034235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8898790 | ATACTCCTGTTTCCC[A/G]AGAACTAAGTCCCAC | 7874 |
rs558054338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8954670 | TTCATTTGAGGTTTG[C/T]GTAGTTTAATAACAG | 7874 |
rs558056121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8931456 | CCTCCCAAAGTGCTG[A/G]GATCACCCACCCATG | 7874 |
rs558067772 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8917274 | AACACAATGGCTAAG[A/G]TTGTTGTTAGGGCTT | 7874 |
rs558087495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8931427 | CCTGGCCTCAAGTGA[C/T]CCACCTGCCTTGGCC | 7874 |
rs558092934 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956846 | GAGCCCAGCCCCCCC[A/G]CAGGCAGTGCCCCAT | 7874 |
rs558112287 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964953 | TCTCCTGTCCTGTCT[C/T]ATTCAGTCATTGACA | 7874 |
rs558158811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8946495 | TTAAGTGAATACACA[C/T]GAGCTACAGACCAGC | 7874 |
rs558212929 | snp | G/T | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964306 | CGCCGGGGCGAGCGC[G/T]GGAGGTTGCCCGGGG | 7874 |
rs558222404 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8928339 | GGACACAGGACACTC[-/A]AAAAAAGGGGGAGCT | 7874 |
rs558259484 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8898141 | GGGAAGGGTTGGCTG[C/T]CGAATGGTTCCTTAG | 7874 |
rs558261831 | in-del | -/C | 0.00440968 | 0.0467482 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956781 | AAACAAAAACAAAAA[-/C]AAAAAAAACACTGAA | 7874 |
rs558338811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8933209 | CCTCTCAAAGTGCTG[A/G]GATCACTCATGAGCC | 7874 |
rs558356619 | snp | A/C | 1.67719e-05 | 0.0028958 | intron-variant | USP7 | GRCh38.p7 | 16:8898339 | ATAAAAATTAAAATT[A/C]ATAGTATTAAAAAAA | 7874 |
rs558380054 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961146 | AAAGTAGCCTTGAAA[A/C]CGTGCATGGAGACTG | 7874 |
rs558400644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8926659 | ATGTATTATTTTTTT[A/G]CAACTTCCAAGTATG | 7874 |
rs558433335 | snp | A/C | 0.0023933 | 0.0345097 | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891809 | TGTGAGGGCGTGGGA[A/C]GGGCCACTGTGACCG | 7874 |
rs558433402 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8896009 | ACTGGGCTGATTTTT[G/T]CATTTTTAGTAGAGA | 7874 |
rs558448982 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956502 | AGGCGCAGTGGCCCA[C/T]GCCTGTAATCCCAAC | 7874 |
rs558497473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8905035 | AGTCTGCATCGAAAC[A/G]CGCAAGCCCAACCCT | 7874 |
rs558518771 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8936917 | CTGGTTTAAAACACT[G/T]TATCAAACACTGGTG | 7874 |
rs558568467 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, nc-transcript-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8892067 | TGGAAAAGGGAACGC[C/G]GCAGATGACGGAAAC | 7874 |
rs558626572 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8911431 | AAGGGCGAGCCACAT[G/T]CTGAGTGACAAGCTC | 7874 |
rs558660231 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8946035 | GATCCCATTTGATTT[C/T]TGACAAAGGTACAAA | 7874 |
rs558676439 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | USP7 | GRCh38.p7 | 16:8901332 | AACGAAAAAAAAAAA[A/C]CAGTAAGCTGAATAG | 7874 |
rs558676887 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8947090 | TAAAGCATTCCTCCT[G/T]TTTTTTTCAGTATAT | 7874 |
rs558680310 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8956048 | CCAAACTCACACAGC[A/G]CACTTTCCAAACCAG | 7874 |
rs558699481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8906345 | CTGACAAGGTTCCGA[A/G]TAGGAACCAGAACAG | 7874 |
rs558767214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8928769 | GAAGGGCATTTCCAC[C/T]TTCGGGTCCTATGGC | 7874 |
rs558781065 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8929965 | CGTATCTTGCTGCAA[A/T]CAAACAAGAAGGAGA | 7874 |
rs558829665 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960471 | AGAGCAAACTCACAC[G/T]GACCTATTGATAGAG | 7874 |
rs558833118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8922009 | TTCCTGCTTGCTCGG[A/G]ACGCTGACACTGGGT | 7874 |
rs558849863 | in-del | -/TGT | | | intron-variant | USP7 | GRCh38.p7 | 16:8915998 | TGAACAGCCATTTCA[-/TGT]TGTGTGTGTGTGCTT | 7874 |
rs558939796 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8924342 | TTGCCACAGCAAAGT[A/C]AACATGCTACACAAG | 7874 |
rs558971614 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8902240 | ATGGCTTAGGTGACA[C/G]AGCGAAAAACTACAG | 7874 |
rs558975663 | in-del | -/G | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961504 | CTCAAAAAAAAAAAA[-/G]GGGGGGGGGGGGCAA | 7874 |
rs559018747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8947396 | TCTTATCACCCAGGC[C/T]GAAGTACAGTGGTGC | 7874 |
rs559049350 | snp | C/G | 0.0700422 | 0.173537 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956794 | AAAAAAAAAAACACT[C/G]AATTTGCTTTACACA | 7874 |
rs559054457 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8912779 | ATTATAATTAATTGA[A/T]AAATACATAGAAAAA | 7874 |
rs559105835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8917385 | ATAAATTTTGAAAAT[C/T]ACCACCCACGTGACA | 7874 |
rs559117121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8930893 | AAAATCACTTGAACT[C/T]AGGAGGCGGAGGCTG | 7874 |
rs559193421 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8926786 | CCATTTCATTACCGC[A/G]TGCTTCTTTTTACTG | 7874 |
rs559228683 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8931177 | TAAACGTTTTCATCA[A/T]GAACACATGCATCTT | 7874 |
rs559276188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962294 | TTTTAAAGACCATTT[A/G]GACTTTGCTTTGTTT | 7874 |
rs559277308 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8935570 | GACATGTTTGGCAAA[C/T]ACAAGTGACTATGTG | 7874 |
rs559303703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8927266 | GGCAGAGGGTGAGGT[A/G]AACCGAGATTGCGCC | 7874 |
rs559336961 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8938983 | AATCCACCATTAATA[C/T]CAAGGGACAGGGAGA | 7874 |
rs559374688 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893255 | TCCTTTCACCTGCTC[A/G]TATGAACTGTTGAGA | 7874 |
rs559379719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8898674 | ATAAATAAATGACTT[A/G]TTTATTTGCCTAAAA | 7874 |
rs559423654 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8943975 | TTTTAAAGCAAAACT[A/G]TAAGGTGCGGGGGAG | 7874 |
rs559516601 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8940839 | ATCCAAGCTACTTGG[C/G]AGGCTGAGGCAGGAG | 7874 |
rs559516898 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8945622 | GAGACAGCACAGTAA[A/T]GATGTTCTCCCCAAA | 7874 |
rs559539518 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8958393 | AGACTGCAGCTGTGC[A/G]ACTTCCTGTAGAGAA | 7874 |
rs559542101 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8898066 | CGGCAGGAAGAGCTG[C/G]AGAAGGATCCTCCTC | 7874 |
rs559551822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8945299 | TGAGGCACAAGAATC[A/G]TTTGTACCTGGGAGG | 7874 |
rs559597167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8955098 | CTTTCTATGAATCTG[C/T]AGTTTCTGCAATTCT | 7874 |
rs559628082 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8941355 | GTGGACATACCCTAC[A/G]TATCCTGCAGTCTGC | 7874 |
rs559635484 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8922501 | ATTTTATTCCCTGGG[C/G]GATCTGACAGAACAG | 7874 |
rs559644196 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961234 | GCGATGGCTCACACC[A/T]GTAATCTCAGCAGTT | 7874 |
rs559672177 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8958696 | AGTGTTCCACTTCCC[C/T]ACACTCATCGCAGGG | 7874 |
rs559703724 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8929225 | ATGCACTCACTCAAC[C/T]GCTTTCGGCATCTCA | 7874 |
rs559751294 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8916108 | GCTGAGGTCTGCTCA[A/G]TGAGAACCTCGCTGC | 7874 |
rs559765639 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8936511 | ACTTCAGAAGTTTGG[C/T]TGAGACATGTCAGTA | 7874 |
rs559796133 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8952629 | TGCAGGCCCACCTCC[A/T]CACTAGGGATCCTGA | 7874 |
rs559813298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894274 | GAGGCCCACACCCTG[A/G]CTGCGCCTCAGAGCC | 7874 |
rs559833566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8959124 | TTAGATGTGCCTGGC[A/G]ATTCCAGTCTCACAA | 7874 |
rs559860410 | in-del | -/AAGACATGGTA | 0.0119091 | 0.0762411 | intron-variant | USP7 | GRCh38.p7 | 16:8934937 | ATTAAAATTTTAATT[-/AAGACATGGTA]AATCCCTAGTCCAGA | 7874 |
rs559864702 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891864 | TTTTCAGGGCTCCCC[A/G]CTGTGAAGACTCCGA | 7874 |
rs559869747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8947691 | TATATGGTAAATAAC[A/G]GTAGCTATAACCCAC | 7874 |
rs559880510 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8924560 | TGAGACTTGTAGGCT[G/T]GGGTAAAGAGTGCCT | 7874 |
rs559895201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8956135 | TGTCCTCCCAATATC[A/G]GGATGTCAGGAAACC | 7874 |
rs559898424 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8949998 | AAACAGCAGTGCTGT[C/T]CCACCAACCATAGAA | 7874 |
rs559913017 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8932865 | ACATGTATATTTAAA[C/T]TTAAGAATATATTTA | 7874 |
rs559951608 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8920985 | TGAATCCAGAAAGCT[A/G]CTAAAAACGTAAGAT | 7874 |
rs559993228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8904609 | CCTGCAGATGGACTT[C/T]CCCCTCTTAGAAGCT | 7874 |
rs560001079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8936050 | CCCCCAAAAAGCTGG[C/T]AGGGGGCGGGGGTCG | 7874 |
rs560045412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8943006 | GGTCAGCCGACCACC[C/T]GGCTTTAAGGCAGTG | 7874 |
rs560095777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961790 | ACACAAAATTCCCTC[A/G]GTAAAGTACTTCTTT | 7874 |
rs560157132 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8931923 | ACCAACAGAAATTAA[C/G]AATCTCAACTGCATA | 7874 |
rs560183861 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8906133 | GGGCCCACCGCATGG[C/G]TAATTATCCCACGAG | 7874 |
rs560193845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8907184 | TTCTGATTCCTAAAC[A/G]ATGCCCAAATCTGAA | 7874 |
rs560200578 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8892176 | GCCAACCCCCAGCCC[A/T]GAACAAAAACAAGAC | 7874 |
rs560222196 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8895869 | TTTGAGACAGTCTCA[A/T]TCTGTCGCCCAGGCT | 7874 |
rs560242393 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8924983 | TAATCCTTTTGAGGA[C/T]AGAAGTCTACTAAAA | 7874 |
rs560277695 | snp | A/G | 0.000115543 | 0.00759988 | missense, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8930313 | TCCATGTCCTCCTCC[A/G]CGGTGTTGTGTCCAT | 7874 |
rs560281298 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893003 | ACCGAAATAAAACTA[C/T]ACACAATGAATATCA | 7874 |
rs560345254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8897215 | CCCCAGCTGGCCCCC[A/G]TGTTCTTGCTCTCAT | 7874 |
rs560345318 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892688 | AGTACATCTCAGTGA[A/G]ACCTTGTTACAAATG | 7874 |
rs560366459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8902825 | ACCAAAAGGCGGAGG[C/T]TGCAGTGAGCCAAGA | 7874 |
rs560368724 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957111 | TTCCAACTTCCAAAT[A/G]AAAAGTTAAAATTAC | 7874 |
rs560376080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8916966 | TTCTCTACTCACTTG[C/T]CCTAAAAAAAAAAAA | 7874 |
rs560423906 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8926011 | TACAAAAAATTAGCC[A/G]GGTGCAGAGGCTGGC | 7874 |
rs560473483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8911518 | TCATGAAGGAAAAAC[A/G]CAACTGCACAACACT | 7874 |
rs560473635 | snp | C/G | 1.64909e-05 | 0.00287144 | intron-variant | USP7 | GRCh38.p7 | 16:8916493 | ATACAAGTATTGCTT[C/G]AAACTTACCACTCGA | 7874 |
rs560482926 | in-del | -/AC | 0.00795532 | 0.062565 | intron-variant | USP7 | GRCh38.p7 | 16:8947356 | GCACTCCCCCCCCCA[-/AC]ACACACACACACACA | 7874 |
rs560494885 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8944728 | TTAATCCCCTTTAGA[A/G]GGGACCTACTCAGAC | 7874 |
rs560507169 | in-del | -/AA | 0.30074 | 0.244797 | intron-variant | USP7 | GRCh38.p7 | 16:8901323 | AAACAAAAAAACGAA[-/AA]AAAAAAAACAGTAAG | 7874 |
rs560507838 | snp | C/T | 1.67055e-05 | 0.00289006 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8902403 | TTGCCGTCGGCTTCA[C/T]TATCTAACATTGCTG | 7874 |
rs560541606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8930493 | GATGTTGCCTAATCA[C/T]TAATAAATTCCAATT | 7874 |
rs560545311 | snp | C/T | 6.6011e-05 | 0.00574466 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8906492 | ATCTCCACTATGAAC[C/T]AGGACTGCATGAAGA | 7874 |
rs560564753 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961693 | GGATATTTGTCTTGA[C/T]CGGGTACCATTTGAA | 7874 |
rs560585045 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8921768 | CGAATTCACGATGAG[A/G]CACAAAATTACAACC | 7874 |
rs560590064 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8922651 | CAGACAGGTTGACAA[A/G]GTGGTCCGTACTCCC | 7874 |
rs560643582 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | USP7 | GRCh38.p7 | 16:8953600 | CCATGCGGCGCCACC[A/G]GAAGCAGAGGGAAGA | 7874 |
rs560644629 | snp | A/C | 1.66704e-05 | 0.00288703 | intron-variant | USP7 | GRCh38.p7 | 16:8899231 | TTTGGGGAAAAATTG[A/C]AACTTGGTCATAAAC | 7874 |
rs560679797 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8898902 | AGATGCACTGAGGAT[A/G]TATCTAAAGTCAGTC | 7874 |
rs560727689 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8909249 | GCCCTCACTCCATGT[C/G/T]TGACTCACAGCTCTA | 7874 |
rs560751205 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8940739 | TGAGATCAATCCCCT[A/C]TGCGAGGCCTCTCCT | 7874 |
rs560807254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8918696 | TGCCTGTAATCCCAG[C/T]TACTCAGGAGGCTGA | 7874 |
rs560825587 | snp | C/T | 0.00835141 | 0.0640778 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937228 | TAAAAAAAAAAGGAT[C/T]AACACGAAACAACGT | 7874 |
rs560864905 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8936020 | TCTGCCACTTCACGA[A/G]GATTTATCAATCCTC | 7874 |
rs560967056 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8936359 | GCATGGTCCTCTCTT[C/G]ACCTCTCATCTCCTC | 7874 |
rs560968075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8914127 | AAAATTGTTAAAGTA[C/T]TTAAACAAGCATTTT | 7874 |
rs560969975 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8918952 | GGAGACGCCATGTTT[C/G]TTGAGAGGACTTTGC | 7874 |
rs561006438 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8948857 | CAGTTCCAGCTACTC[C/G]GGAGGCTGATGGGAG | 7874 |
rs561066906 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8929977 | CAAACAAACAAGAAG[A/G]AGAGTAAGACATGCT | 7874 |
rs561084227 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8920293 | CTCTATTACATGCAC[A/G]CTAAAGCTTCTTTCA | 7874 |
rs561084559 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8930974 | CTCAGTCTCAAATTA[-/A]AAAAAAAAAAAAAAA | 7874 |
rs561143229 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8932803 | ATGGACAAAGCAGGA[C/T]AGTGCCTTATCTGCG | 7874 |
rs561146684 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950653 | TGTCTGCCACGAACA[C/T]GGCACTGCTAATTGT | 7874 |
rs561196815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8923724 | AAGGACCCCAGGCAC[C/T]AAGTGAGTGGAGAGA | 7874 |
rs561211066 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8955572 | TTAGCCGGGCATGGC[A/G]GCGCGCCCCTGTAGT | 7874 |
rs561219592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8928846 | GGGGACTTTACCCAT[A/G]TTGTCCCCTCATAAG | 7874 |
rs561221459 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8898446 | TCTTAAGCTATTAAG[-/A]AAAGAAAGATTCACA | 7874 |
rs561222179 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8946306 | AAAAAAATGGCAGGC[A/G]GCGGTGGCTTAAGCC | 7874 |
rs561222349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8910525 | CCCACAAGACCCTCC[A/G]GACTGCTGGATGTGC | 7874 |
rs561256302 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8933369 | ATGGGCAATATAGTG[A/G]GATTCCCAACTCTAT | 7874 |
rs561261022 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8913825 | GCACAATCATGGCTC[A/G]CTGCAGACTTAAACT | 7874 |
rs561299523 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893451 | AAGCCCCCAGGCAGC[C/T]GGAGGAGGAGAACCC | 7874 |
rs561307632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8951489 | TCGCCCTGAGCCAGC[C/T]GGATTCATGTGATGA | 7874 |
rs561329931 | snp | A/G | 3.29457e-05 | 0.00405854 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8905278 | CCCATAATTGTGCTC[A/G]ATTGCTTCCTCTTTA | 7874 |
rs561363601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8916636 | ACTTAGATTGAAAAC[C/T]TAAACTGGATAATCA | 7874 |
rs561383714 | snp | A/G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8941914 | GCAAGTCCCTTGGTG[A/G/T]TCATTGCAATAGAGG | 7874 |
rs561423364 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8900448 | GTGGCTCGGGATCTA[C/G]GTACAAATGTTTCTT | 7874 |
rs561530563 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8912589 | CAGAATTAGTAGACA[A/G]GAGCATTATCAACTA | 7874 |
rs561545766 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8953274 | TGCACACGTGTTCAG[C/G]GCTCCTTCACTTTCT | 7874 |
rs561566547 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8947926 | GCCACATGCCATTAT[G/T]CCTGGGGATTTCTCT | 7874 |
rs561574496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8939194 | TCCACTACCACCACA[A/G]TTAAGATCCTGAACA | 7874 |
rs561576032 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8892962 | CAGCTGGCATTAGCT[C/T]CAAAATAAAAGGAAA | 7874 |
rs561618179 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8948445 | CGGCCTCGGCCTCCC[A/C]AAGTGCTGGGATTAC | 7874 |
rs561705495 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8953275 | GCACACGTGTTCAGG[C/G]CTCCTTCACTTTCTG | 7874 |
rs561714787 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8953828 | CGTGCCCCCTGCGGC[G/T]CCACTGGAGGCAGAG | 7874 |
rs561740086 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8912720 | TGGGCACAGGACCTC[C/G]GAGACTAGCCTGGCC | 7874 |
rs561827686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8954466 | TTCGGGTCATGGGCA[A/G]TGGGACCACAATACA | 7874 |
rs561832985 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8902898 | AAAGAAAAAAAGACT[C/G]TGATTCTAAGAAAAA | 7874 |
rs561896819 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8958636 | GAGTTCAAAGCCGAC[G/T]CCCAACGTCTGGACA | 7874 |
rs561897644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8949807 | CAAGCCCCCAGGGCC[C/T]GAAGCAGTGATTACC | 7874 |
rs561942257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8903243 | GGGAGCCACGGTGGG[A/G]TATATCCACGGGACC | 7874 |
rs561958968 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8948926 | CTATGATCAAACCAC[A/G/T]GCACTCCAGCCTGGG | 7874 |
rs562003619 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8963962 | GAGAGCAAGCGGGCG[A/G]GCGCCGAGCCGGAGG | 7874 |
rs562033737 | snp | A/G | 3.30442e-05 | 0.0040646 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8898540 | TCATACCTGCTGATA[A/G]TAAAGTTTCTTAGGT | 7874 |
rs562049877 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894241 | AGGACCTGAGCTACA[C/G/T]GCCCACCTGGAGCTA | 7874 |
rs562084701 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893720 | CCCGATCCACTAACC[C/T]CTTCTCCCCCATTGC | 7874 |
rs562099048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8926354 | TGTGGTGGTGCACGC[C/T]TGTAATCCCAGCTAC | 7874 |
rs562115266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8958392 | AAGACTGCAGCTGTG[C/T]GACTTCCTGTAGAGA | 7874 |
rs562211640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8921851 | CTCTAGATCCAGGTT[C/T]AAAAACCATACATAC | 7874 |
rs562260994 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8944977 | GCTGGGTGGACCGGG[C/T]GCAGTGGCTCACGCC | 7874 |
rs562289964 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8917812 | GTTTTGTTTTTGAGA[C/T]GGAGTCTTGCTCTGT | 7874 |
rs562295488 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8952575 | GGTCCCCTCACTCTG[C/G]CACTGATGACTGTGA | 7874 |
rs562318300 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8908101 | AGCCATAGCTGAGAG[C/G]AGGGCTGGGACTGGG | 7874 |
rs562395939 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8918093 | CTGCGCCCAGCCATG[C/G]AGCACCATTTCTTAA | 7874 |
rs562396076 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8913305 | AGGTTGCAGTGAGCC[A/G]AGATCGCACCACTGC | 7874 |
rs562399169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8908608 | CATCTTTGAAATGTT[C/T]TCTTTAGGTCTGTTT | 7874 |
rs562405934 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950447 | TCCAAAGGAAATACT[A/G]ATCATTAAGAGTAAA | 7874 |
rs562407054 | snp | C/T | | | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8910781 | GTCGTATTTATTGTC[C/T]CCATCGAGCTGTTCT | 7874 |
rs562433985 | in-del | -/AC | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950604 | CAGGACTGGGCGCTG[-/AC]AGAGACAACAGTCTC | 7874 |
rs562481338 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8933279 | CCAAGCACAGTGGCT[A/C]ATGCCTATATAATCC | 7874 |
rs562504022 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8900406 | AAGCCTCTCAACAGT[C/T]ACATTAAAAAAAACA | 7874 |
rs562504901 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8918257 | AGCCAGCCAGCTCCC[-/T]TGCCCACCCCACAAC | 7874 |
rs562519417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8924442 | GGAGTCCCAGGGCCA[C/T]ACCAAGGGCCAAGCT | 7874 |
rs562621084 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8901637 | CATTTTATAGCAAGG[C/G]TCAGCAAATTCCGAT | 7874 |
rs562642346 | snp | C/T | 0.000804991 | 0.0200461 | intron-variant | USP7 | GRCh38.p7 | 16:8916000 | AACAGCCATTTCATG[C/T]TGTGTGTGTGTGCTT | 7874 |
rs562643211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8928835 | CTCAAAAGGAAGGGG[A/G]CTTTACCCATATTGT | 7874 |
rs562652557 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8942301 | TGGAGAGTCTGTCGG[A/G]CCTGAGACAGCCCCA | 7874 |
rs562670555 | snp | A/G/T | 1.64844e-05 | 0.00287087 | intron-variant | USP7 | GRCh38.p7 | 16:8915416 | CTAAAACCTTTAAAA[A/G/T]TCATCTTTTAGAACT | 7874 |
rs562685681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8919719 | GAAGCCACAGAGAAC[A/G]GTGCCAGAAAGCAAA | 7874 |
rs562767190 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8930889 | AATGAAAATCACTTG[A/G]ACTCAGGAGGCGGAG | 7874 |
rs562794563 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8920809 | ACTGGTTACCACCTC[G/T]GCAAAAAGCAGCCAA | 7874 |
rs562796782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8920015 | CGGAGAGGACTTCCT[C/T]CCTGCCCTCATCAAA | 7874 |
rs562830536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961983 | CCACTTTGTCATTTG[C/T]AACCTGGCCAGCCAT | 7874 |
rs562926421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8942863 | ACTTTGTGATTTTAT[A/G]CCCTCCAGTTATTTG | 7874 |
rs562947718 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8907818 | GACTCTGTCTCAAAA[A/T]CATAATAAAACAAAG | 7874 |
rs562987292 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938535 | GGCTAACACGGTGAA[A/G]CGCCGTCTCTACTGA | 7874 |
rs563020401 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957475 | CGGGCTGGGTGAGGT[A/G]GCTCACACCTATAAT | 7874 |
rs563020718 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8909233 | GGCCAGGCGGTCAGG[A/G]GCCCTCACTCCATGT | 7874 |
rs563020820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8903822 | AGGTGAGCAGAGATC[A/G]CGCCACTGCACTCAA | 7874 |
rs563049068 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8913383 | GAAGAGGGAAGACAG[C/G]AGAGAAGAGAAGTGA | 7874 |
rs563073938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8930086 | ACACCTCCTTGCCTA[A/G]GCTAGGGAGACTCTA | 7874 |
rs563102178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962324 | TCAGTGAAATGGGTC[A/G]TGAGAAAAAGTGCCT | 7874 |
rs563150728 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8952981 | AGCTGGGATTACAGT[C/T]GCGTGTCACCATGCC | 7874 |
rs563193146 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8922526 | GAACAGCCAGAGTCA[A/G]TTCACTCTGGGGAAC | 7874 |
rs563206498 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892641 | AAAAGAAACAAGAGA[A/C]CCTGCCCCCGCAAAA | 7874 |
rs563236171 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8925529 | GGAACTTTCACCCTA[G/T]ACATTAAATTTTCCA | 7874 |
rs563270879 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8940235 | AGGTCACCTGTCTAG[C/G]CATCCTACAGCCAGG | 7874 |
rs563316050 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8931805 | CCTAGGTTCACACAT[C/G]CCATTTAAATCAATT | 7874 |
rs563342796 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8965200 | CCGAAAGAATGTTTT[C/G]CTCACTGTTGTATCA | 7874 |
rs563346021 | in-del | -/A | 0.0103295 | 0.0711199 | intron-variant | USP7 | GRCh38.p7 | 16:8917241 | TTAATCTTCATGTTT[-/A]AAAAAATCATTTCTA | 7874 |
rs563360623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8918205 | ATATCACGACAACCT[A/G]TCTGGGTGGCTGTGC | 7874 |
rs563372370 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893153 | CTTTTTTACAAAGTC[A/G]ACAGCTTACTAACCA | 7874 |
rs563382387 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8940677 | AAGCTCCTGACCGCC[A/T]TCTTCTAGACATTTC | 7874 |
rs563388152 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964619 | TTTGGGTTTTGTTTT[C/T]ATATTTTTGAAATGT | 7874 |
rs563406783 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8920708 | TGGACAGGAGAAATC[G/T]GTGCCCCTCTAAGCA | 7874 |
rs563440178 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8959156 | AACCTTGACGGGCAT[A/G]AATGACCTCCTTTAA | 7874 |
rs563534892 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8898691 | TTATTTGCCTAAAAA[A/C]AAATATCTGTGAGTG | 7874 |
rs563552782 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8954752 | GGGTCTGAGGTGGGT[A/G]GATCAGGAGATCGAG | 7874 |
rs563558615 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8959801 | GCACAAGTTTGGAAG[A/G]AACCCACCACCACCC | 7874 |
rs563620445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8914005 | AGCCTCCCAAAGTGC[C/T]GAAATTACAGGCATG | 7874 |
rs563650314 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937019 | TCTGTACATCTAGAA[C/T]TACTCCAAAATTAAA | 7874 |
rs563651469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8945341 | GTGAGCCAAGACCAT[A/G]CCACTGTACTCCAGC | 7874 |
rs563740981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8949939 | TCTAACGGTTGCTAT[C/T]CCCTAGAATAGCAAA | 7874 |
rs563792511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8932774 | GAGGAGGCAAGAAGG[A/G]AATGGGGCTGGGGAT | 7874 |
rs563837093 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8904811 | AATAAAAATAAAATA[A/C]AATACAAAAAATTAG | 7874 |
rs563908335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8914619 | TCATGAATGTGCTGG[A/G]CAAAAGGAATCAGAC | 7874 |
rs563936429 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938707 | CACAGCAAGACTCCG[C/T]CTCAAAAAAAAAAAA | 7874 |
rs563942179 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8920227 | GCAGGTGTGACTCTG[C/T]GTGCCACAGGGCAAG | 7874 |
rs563974686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8952682 | CCTTTGCCATGTAAC[A/G]TAACATTTGCAGGTT | 7874 |
rs564035609 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892544 | CCAGTCACCTTATTT[C/G]TACACAGTTCTCTCC | 7874 |
rs564044821 | in-del | -/AAAC | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8901300 | GCTTAAAAAACAAAA[-/AAAC]AAACAAACAAAAAAA | 7874 |
rs564047609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8939146 | ACGTGTATTTAGTTC[C/T]CTACAATTTTATTTA | 7874 |
rs564052656 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8916092 | AGAGTAATCACCGCA[G/T]GCTGAGGTCTGCTCA | 7874 |
rs564055836 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8935836 | TGCCTATACCCAGCT[C/T]TCCTCCCCGTGAATT | 7874 |
rs564071476 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8952954 | CGATTCTCCTGCCTC[A/G]GCCTCCCAAGTAGCT | 7874 |
rs564110984 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957674 | GAGGTGGGAGGATCA[A/C]CTGAGCCCGGAAGTT | 7874 |
rs564113551 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956881 | CACGAGGACTCCCAG[C/T]GCAGCCTCAGCCATG | 7874 |
rs564199106 | snp | C/T | 1.66391e-05 | 0.00288431 | intron-variant | USP7 | GRCh38.p7 | 16:8916591 | CAACTCCATTTAAAG[C/T]TCAACTTTCAAATGA | 7874 |
rs564215651 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8914646 | AGACACAGGCTGGAC[A/T]TGGCAGCTCATGTCT | 7874 |
rs564226520 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8934327 | TGCAGTGAAATCAGA[C/T]TGAGACACAAGTGAA | 7874 |
rs564230419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8947763 | GACAGGATCCTGCCA[C/T]CAAAAACTTAGCTAT | 7874 |
rs564235166 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8928720 | TTACTCAACCTTCTC[A/G]GATTATACGCTTTTT | 7874 |
rs564236337 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8920715 | GAGAAATCTGTGCCC[A/C]TCTAAGCAGGGGAGG | 7874 |
rs564237334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8906642 | AAAAATATCACACTT[C/T]ACAGTAAGTAAGGCC | 7874 |
rs564274483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8911942 | AAAAACCGCTGAACA[C/T]CTGGGAGACTCAGCT | 7874 |
rs564413217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8897899 | GCGAGACCCTGTCTC[A/G]AAAAAGAACCACCTA | 7874 |
rs564429248 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8910950 | AAACAACACTAACAG[C/T]AACTCTCCCCCTGTA | 7874 |
rs564463812 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8930779 | TTCGAGACCAGGCTG[C/G]CCAACATGGTGAAAC | 7874 |
rs564517802 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8902857 | CGCGCCACTGGGCAA[C/G]AAGAGTGAAACTCTG | 7874 |
rs564565828 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8952248 | GGAGAGCCTGTCTCC[-/A]AAAAAAATATTAATT | 7874 |
rs564612771 | in-del | -/GA | 0.00795532 | 0.062565 | intron-variant | USP7 | GRCh38.p7 | 16:8903854 | CTGGGCAACAAGAGT[-/GA]GAAACTCTGTCTCAA | 7874 |
rs564624824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960489 | CCTATTGATAGAGAC[A/G]AAACAAACGAAACAG | 7874 |
rs564650250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8949318 | CACTGGGATTGAAAC[C/T]GAGACATAAAAATGC | 7874 |
rs564662896 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP7 | GRCh38.p7 | 16:8948824 | CAAAACTTAGCCAGG[C/T]GTGGTGGCGTGTGCC | 7874 |
rs564679847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8899997 | TCTCATCCCACTACA[A/G]AACAAAACCCCCTTA | 7874 |
rs564687269 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8921820 | CAGTGAAGTGTGGGG[G/T]GGACCACAAAAGGGC | 7874 |
rs564714308 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8949948 | TGCTATCCCCTAGAA[C/T]AGCAAAGGAAAACCC | 7874 |
rs564728093 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8953398 | ACCAGCCTCTGTGGA[C/T]ACTACAGGACACCAA | 7874 |
rs564737677 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8904771 | CATGGTGAAACCCCA[A/T]CTCTACTACTAAAAA | 7874 |
rs564767713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8895316 | ACTCATGGGAGTCTC[A/G]GCCAGAAGATATCCA | 7874 |
rs564795382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8944589 | AACAGGTTCCTTTAT[C/T]TGAATAAAACCACAA | 7874 |
rs564799487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8922155 | CTTTAACCATCCACA[A/G]GCCCTGGCTGCATCA | 7874 |
rs564817228 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8934271 | AATCGAACTCTACAA[C/T]TGCTCTGTAATTCTG | 7874 |
rs564887888 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8951550 | ATCCTATTTGCTCAT[C/T]TGTAAATGCAGAGGG | 7874 |
rs564927709 | snp | C/G | 3.39818e-05 | 0.00412186 | missense, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8923410 | TCGGAGCGCCAACTG[C/G]TGTCTGCAAAAAAAA | 7874 |
rs564960730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8910580 | TCCATCTCCCAACAT[C/T]CCCCTCTCCCTCCCC | 7874 |
rs564962614 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957333 | GTGACATTTAACATC[A/T]AACTCTGTCATGGTA | 7874 |
rs564975186 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8955336 | TGTGGCCTCGACCTC[C/T]AAGGTTCAAGTGATC | 7874 |
rs564982560 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8955647 | GGAGGAGGAGGTTGC[A/G]GTGAGCCGAGATCAC | 7874 |
rs564983555 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8900368 | TGAAAATGTTCACCA[A/C]ACCTAATTTCAAAAC | 7874 |
rs564992759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8914848 | CGCCTGAGTCCTGGA[A/G]TTCGAGGCTGCACTG | 7874 |
rs564999264 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8932701 | ACATCAAATCTTTAA[A/G]AAGTTTTATGAGATT | 7874 |
rs565073330 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8911043 | CTTTCTTAAGGACAT[A/T]AAAATGACAATATGG | 7874 |
rs565085145 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8940528 | CAGGCAACCCAGGGC[A/G]GGAGGTGGGGCAGTT | 7874 |
rs565098561 | in-del | -/TTA | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8932403 | AGACCTCATCTCAAT[-/TTA]TTATTATTTTTAAAG | 7874 |
rs565110404 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964639 | TTTTGAAATGTATTT[C/T]TAATTAGCCGGGTGT | 7874 |
rs565115857 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8928980 | CAACCAAGAATTATC[C/T]AAGTTGCCATGAGAA | 7874 |
rs565138951 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8944920 | CGAGATCAGCCTGGC[C/T]AATATGGCGAAACCT | 7874 |
rs565146673 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8905961 | CTGGCCCTGTGGTCT[A/T]GGGGGTAGATTCCAA | 7874 |
rs565171303 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891627 | GGCCTCCATCAGGAA[A/G]CGATGGTGTCTAGAC | 7874 |
rs565197749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8946330 | TTAAGCCGGTAATCC[C/T]AGCACTTTGAGAGGC | 7874 |
rs565204493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8952092 | CCCCCCCGTCTATAC[A/G]AAAAAGAAAAAAAAT | 7874 |
rs565227133 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8946244 | AGGGCAAATATTTGG[A/G]CATAATACCAAAAGC | 7874 |
rs565227265 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8923076 | CTTGGATATTATACA[C/T]ATACCAGTGGGTTTT | 7874 |
rs565232248 | in-del | -/GT | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8934289 | CTCTGTAATTCTGAG[-/GT]ACAGGTTATGGTTTC | 7874 |
rs565243147 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937467 | GAATCACTTGAACCC[A/G]GGAGGCGGAGGTTGC | 7874 |
rs565280495 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8929262 | TAAAGTAAAACCTCC[A/G]AAAGCCCAACAACCA | 7874 |
rs565287883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8895925 | CACTGCAACCTCCGC[C/T]TCCCGGGTTCAAGCA | 7874 |
rs565311925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8946606 | GGACAAAACTCAACT[A/G]AAAAGTCAGAATAGC | 7874 |
rs565312158 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8941791 | ACCACCGGCCAGCCA[A/C]TGACCCTTCCAAGCC | 7874 |
rs565349357 | snp | A/C/G | 0.000100485 | 0.00708762 | intron-variant | USP7 | GRCh38.p7 | 16:8900982 | ATGGAAAAATAAACC[A/C/G]TCCAAACCTCATAGA | 7874 |
rs565350384 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938141 | GAAGAATGGAAAAGT[A/C]CTGAGCAAACAGGCA | 7874 |
rs565404571 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893439 | AAGTTTATTAAAAAG[C/T]CCCCAGGCAGCTGGA | 7874 |
rs565405490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8930661 | GATATTCTGCACAAA[A/G]CTTTTTATATAAAAT | 7874 |
rs565443070 | snp | A/G | 1.73405e-05 | 0.00294448 | intron-variant | USP7 | GRCh38.p7 | 16:8930402 | TGTATCTCCCGCTTT[A/G]AAGAAGAAAAAGAAA | 7874 |
rs565487549 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961301 | AGTTCGAGACCAGCC[C/T]GACCAACATGGAGAA | 7874 |
rs565518342 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8926149 | ACAGAGCGAGACTCC[A/G]TCTCAAAAAAAAAAA | 7874 |
rs565534377 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8939250 | AGTGGCCCTGTTACG[A/C]CCACCCACCCCGGCG | 7874 |
rs565567296 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893562 | ATGCACAAAAGGTCA[C/T]TGAAAGTATAACTGA | 7874 |
rs565580344 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8916765 | TAATAAATCTGAAAG[A/C/T]AGTACAGGTTCTTGT | 7874 |
rs565635503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8902922 | AGAAAAAGAATTCTA[A/G]TTCTTCCCCGGTTGA | 7874 |
rs565673681 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8907278 | AAGTGAGGATCCAAA[A/G]AAACATACCAACAGG | 7874 |
rs565695054 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8944749 | CTACTCAGACTCTCA[G/T]GGAACACCTGCAATT | 7874 |
rs565701709 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8938920 | GTTTTGTATGAGGAA[C/G]ACTTGAGCATCTGTG | 7874 |
rs565712565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8958406 | GCGACTTCCTGTAGA[A/G]AAGGCAGGACACCAA | 7874 |
rs565775299 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962818 | CGCCCGGGGAGGTCA[C/G]GAATTCCCCAGCCAC | 7874 |
rs565780855 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | USP7 | GRCh38.p7 | 16:8948968 | TGTCTCCCAAAGGGG[A/G]AAAAAAAAAGCTTAC | 7874 |
rs565802796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8902649 | AATCCCAGCACTTTC[A/G]GAGGCCGAGGCAGGT | 7874 |
rs565814099 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957561 | CCAGCCTGAACATAG[C/G]AAGACCCCATCTCTA | 7874 |
rs565818427 | snp | C/T | 0.111224 | 0.207945 | intron-variant | USP7 | GRCh38.p7 | 16:8954028 | CCCATGCGGCGCCAC[C/T]GGAGGCAGAGGGAAG | 7874 |
rs565841749 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8953506 | GGAGAAGACACGTGC[C/T]CCATGCGGTGCCACT | 7874 |
rs565858658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8945031 | CCAAGGCAGATGAAA[A/G]ACCTGAGGTCAGGAG | 7874 |
rs565919965 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8917224 | TAAAAAACAGTAAGA[A/C]TTTAATCTTCATGTT | 7874 |
rs565921117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8917501 | CTCCTGCCTCAGCCT[C/T]CCGAGTAGCTGGAAT | 7874 |
rs565972268 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893814 | AAAACATCTTCATTT[G/T]GCTCAAAAAGGGCAG | 7874 |
rs565993351 | in-del | -/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8947346 | TTTTTCCACAGCACT[-/C]CCCCCCCCCAACACA | 7874 |
rs566009255 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8918901 | TGAAAACGCAGCATG[A/C]ACTAGCAGCCATCTG | 7874 |
rs566029157 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8965445 | AGCTACTCAGGAGGC[C/T]GAGGCAGGAGAATCA | 7874 |
rs566107028 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8952970 | GCCTCCCAAGTAGCT[A/G]GGATTACAGTCGCGT | 7874 |
rs566133523 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8935712 | TGATTGCTAGGCCTT[G/T]TAACGCAATATGTAT | 7874 |
rs566146451 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8903044 | GGAAAAGGGGTGAAA[A/G]CATGTCTGCAAAATC | 7874 |
rs566176027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8940384 | CCAGCCTCCAGCACA[A/G]TGCTCAGGAGAACTC | 7874 |
rs566177526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8951673 | CTGGGTATGCTGAGA[C/T]GCTGTGCACCTGCAC | 7874 |
rs566181478 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8926927 | AGGGGCAGGGACAAT[C/T]ACCTACAGCACGAAG | 7874 |
rs566205489 | in-del | -/AA | | | intron-variant | USP7 | GRCh38.p7 | 16:8900823 | GATTCTACAACAGGT[-/AA]AAAAAAAAAATTCAC | 7874 |
rs566210281 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8946694 | GTCACTGGCCTATAC[C/T]CCAGCCCCACACACC | 7874 |
rs566226271 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8913013 | TGGGGGTAACCTCAG[A/G]CAGCCAGAATCAAAC | 7874 |
rs566234437 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8943463 | TTAGGGCAAGGGATG[A/C]CCCTACCTGGATGGA | 7874 |
rs566249505 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP7 | GRCh38.p7 | 16:8899891 | CAGGTTCCCCTTTGA[A/G]GGGGCCAGGCATCTG | 7874 |
rs566280100 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8904219 | AAGCTCAGGAGAGCA[C/T]GTGGAGCAGCTTCTC | 7874 |
rs566287371 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8903531 | CTTCTTCAGAAGACC[A/C]ATGAAGAAAAACCGC | 7874 |
rs566291796 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8935432 | GCCAGGCTGGTCTCG[A/C]ACTCCTGACCTCAGG | 7874 |
rs566420149 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892315 | CTCACTCCCTGCTTT[C/G]TATCACACGGGTCAC | 7874 |
rs566428910 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961425 | TGAACCCGGGAGACG[C/G]AGGTTGTAGTGACCC | 7874 |
rs566444904 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8919201 | GCTCCTGCAGTGTGT[C/G]TGAAGCAATCTGACT | 7874 |
rs566458499 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8955974 | ATGTCAGATTACCAC[C/T]CAGACACTTGCAGCC | 7874 |
rs566483667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8896572 | GTTGGCTAGATGGAA[C/T]AGAAGTGACTCAATC | 7874 |
rs566491178 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8927809 | CCACTGTACTCTAGC[C/G]TGGGCGACACAACAA | 7874 |
rs566509425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894284 | CCCTGACTGCGCCTC[A/G]GAGCCACTGCCCTCA | 7874 |
rs566529604 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8902717 | ACATGGTGAACTCTC[A/G/T]TCTCTACTAAAAATA | 7874 |
rs566539267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8962046 | GTTATTCTATTCAGA[A/G]GTGAACACCAGTCAC | 7874 |
rs566573567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8905483 | ACAGGCACACAATCT[A/G]ACGGTGTGCTAGGCA | 7874 |
rs566595539 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8896082 | CTGACCTCGTGATCC[A/G]CCCGCCTCGGCCTCC | 7874 |
rs566603058 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8900211 | AGACTGAAATGAATT[A/G]CCCAAGTAGGTACAT | 7874 |
rs566617647 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937567 | AAGTTGGGTGTGGTG[A/G]TGCACACCTGTAATC | 7874 |
rs566761134 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8901722 | ATAGTCTTTGTGGCC[A/G]CCTTAGTACAGACAG | 7874 |
rs566765132 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956453 | AACAGTGTCTCCACC[C/T]GTCAAGGGGCATGCT | 7874 |
rs566791485 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8933620 | TGTGTATGCGCTATC[A/T]TTTTTTTTTCCTCAA | 7874 |
rs566791835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8905795 | GGGCCAGACTGAAGT[C/T]AACGTAGCATGTTCC | 7874 |
rs566856358 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8965246 | CACAGCAAGTGCTCA[A/G]TAAAAATTGGTTGGG | 7874 |
rs566869772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8911706 | GGAGCTCAAGGGAGC[A/G]GGAACCTGCTGGGCA | 7874 |
rs566871631 | snp | C/T | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8916711 | GTCATAATTCAAAGA[C/T]AGATTTACTGCTGGG | 7874 |
rs566904028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8929120 | GACCCGGAATGTTCC[A/G]ATAGGGCAGGGCCTG | 7874 |
rs566904096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8933967 | TCACCATGTTGGCCA[A/G]GCTGGTCTCAAACTC | 7874 |
rs566913276 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | USP7 | GRCh38.p7 | 16:8925620 | ACTTGGTTCACCTGC[G/T]GCCCAGCCCCGCAGA | 7874 |
rs566929385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8904078 | ACAACCAAGTCTTTA[C/T]TCCTGAACTGGCTCT | 7874 |
rs566934526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8920882 | ACTATGCCTGAATCA[C/T]GAAAGGACCTCAAAC | 7874 |
rs566937616 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964689 | GACAGCTACTTGGGA[G/T]GCTGAGGCTGGAGGT | 7874 |
rs566938657 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8952835 | CGCCTGTGACCACAC[A/T]CGCTTTTTTTTTTTT | 7874 |
rs566941756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8898200 | CAGGAGGTCCTGCCA[A/G]GAGGCAGGAAAGACT | 7874 |
rs566951994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8906127 | CCGACTGGGCCCACC[A/G]CATGGGTAATTATCC | 7874 |
rs566998583 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8952988 | ATTACAGTCGCGTGT[C/T]ACCATGCCAGGCTAT | 7874 |
rs567014338 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964982 | CAGACTGATGATTAG[C/G]GTCTCAACTTTTCCA | 7874 |
rs567106072 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8917924 | CCTCCCCAGTAGCTG[C/G]GACTACAGGTGCACG | 7874 |
rs567113543 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8947376 | ACACACACACAGGGT[C/G]TCACTCTTATCACCC | 7874 |
rs567117869 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960346 | TTTCCTAACTGCTCA[C/G]GGCATTTCAAAAAAT | 7874 |
rs567190213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8943548 | GCCATGAGAAACACA[A/G]ACGACTAACCAACAG | 7874 |
rs567223980 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8922385 | CCCAGCTACTTGAGA[C/T]GCCGAGGCAGGAGAA | 7874 |
rs567244316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894336 | CTGCACACATATCCA[A/G]GCTTCTCTCCTTGAA | 7874 |
rs567249614 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8926521 | CCAAAAAAAAGGAGA[A/C]GTGGACTTGGAAATT | 7874 |
rs567267358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8918291 | GAGTGCCGATTTCCT[A/G]TACTGCTTCATAATA | 7874 |
rs567267949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8931301 | TCAAACTATTCTCCT[A/G]CCTCAGCCTCCTGAG | 7874 |
rs567337391 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8916635 | AACTTAGATTGAAAA[C/T]CTAAACTGGATAATC | 7874 |
rs567346238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8943425 | GCAGCACGCACGGCC[A/G]GAACCGAGCTGCACA | 7874 |
rs567360999 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8954570 | GAAGACAATTTAGCT[G/T]TAAGTTTATAGGATG | 7874 |
rs567374134 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8918619 | GTTCGAGACCAGCCT[A/G]GACAACATGGTGAAA | 7874 |
rs567398102 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8921400 | CCCATTTATGATTTC[A/T]TTGCTCTCTCCTTTC | 7874 |
rs567422159 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8945101 | TACTAAATAAAAATA[A/C]AGAAATTAGCTGGGT | 7874 |
rs567456766 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8954784 | CCATCCATGGTAAAA[A/C]CCCCCCTCTACTAAA | 7874 |
rs567469324 | snp | A/G | | | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894094 | CCAAGGCCGAGGATG[A/G]GACATATTACCTGGT | 7874 |
rs567474009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8949537 | CCACCCAGAAGCCTT[A/G]CCGCTGCCATCCTTA | 7874 |
rs567490269 | snp | A/G | 1.64811e-05 | 0.00287059 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8897090 | GCTTGTCTGGATATA[A/G]TGTTATTTCCTAAGT | 7874 |
rs567596163 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8941007 | CAGGACCCTTCTTCT[C/T]GTCCAGCACTCAGGG | 7874 |
rs567611304 | in-del | -/G | 0.00597247 | 0.0543191 | intron-variant | USP7 | GRCh38.p7 | 16:8901941 | TATTTGACTTCATCA[-/G]GAAGTCTAGTGAGCT | 7874 |
rs567627555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8928443 | GACAACCCTGAGACA[C/T]ACGACAGTAAATAAA | 7874 |
rs567687326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8904668 | AATCTATTAGGCCGG[C/T]GTGGTGGCTTACGCC | 7874 |
rs567737464 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8905504 | GTGCTAGGCAGGCAG[A/C]GCCTCAGGCATCCGC | 7874 |
rs567742321 | snp | A/G | 1.65556e-05 | 0.00287707 | intron-variant | USP7 | GRCh38.p7 | 16:8899579 | GGAGTGGGATCTGAA[A/G]AGGAAAGGAGCATTT | 7874 |
rs567743956 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8904890 | GGCAGGAGAGTGGCG[A/T]GAACCCGGGAGGTGG | 7874 |
rs567763679 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8944127 | GTAGTTCCCTCTGAG[A/G]AACAGAAACTCTCCT | 7874 |
rs567779098 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8909911 | AGCCTGGGGAACAGA[C/G]CGAGTCTCCGTCTCA | 7874 |
rs567837755 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8934079 | TCTTAAAAGTAATTT[C/G]CTAGACGTACACCCA | 7874 |
rs567870715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8923564 | AATTTATTAAAACCC[A/G]AAGACTGAGATAACA | 7874 |
rs567917088 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8943516 | AAGGATCAACACCGA[C/G]AATGCAGGGCCCCAA | 7874 |
rs567918404 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8923842 | TTTACAGAGCACGGA[A/T]CACACAGGCAGGACT | 7874 |
rs567933909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8955773 | TATAATTTATTCCCC[A/G]AAGTCTTATTGATGA | 7874 |
rs567934463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8918830 | GAAAAAGGTTGGCGG[C/T]GGTAACTCTGAATCA | 7874 |
rs567952867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8895430 | TCTAAATTCAAGTGA[C/T]CCACAGTTTCTGTCT | 7874 |
rs568056619 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8906742 | ACGTAATCCGTACTT[G/T]ATAGAAATAACTATT | 7874 |
rs568065703 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8911565 | CGCTCCGGACACATG[A/C/T]GGTACAGGACAGGGA | 7874 |
rs568088134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8943100 | TGTAAATTAGCTATA[C/T]GAAAACCAAGCCCCA | 7874 |
rs568091461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8911995 | CAGGTTATCCCTCAA[A/G]TAAAACCTGTTCTCC | 7874 |
rs568155610 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8901910 | CCTCACAGGAAACTC[C/G]CAGCCAAGTCAGTCT | 7874 |
rs568177838 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8906257 | TTTACTATTTACCTT[A/C]AAATCTCAGCAATTA | 7874 |
rs568236615 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8926102 | AAGCTTGCAGTGAGC[G/T]GAGATCGCGCCACTG | 7874 |
rs568252967 | snp | A/C | 0.00795532 | 0.062565 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957774 | AAATTAAAAAAAAAA[A/C]AAAAAAAAATTAAAA | 7874 |
rs568260635 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962509 | TTCTGATGCAGGCAG[A/C]CATGTGCGGCAGGGC | 7874 |
rs568267590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8902635 | TGGCTCTCGCCTGTA[A/G]TCCCAGCACTTTCGG | 7874 |
rs568289646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962719 | ACGCTAGGCAGTGCT[A/G]TTAGAAAGTGATTTG | 7874 |
rs568407967 | snp | A/G | 1.68704e-05 | 0.00290429 | intron-variant | USP7 | GRCh38.p7 | 16:8903439 | CAGAAAAGACTTGAC[A/G]ACTGACAAAAAATGA | 7874 |
rs568450181 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8921429 | TCGGGTTGGGGTTAA[A/G]GGTAGGATGGAGGCA | 7874 |
rs568478540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950811 | CACTGACCAGCGCAC[A/G]ACAGTGATCTGAGCG | 7874 |
rs568500837 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8912497 | ACATTACCAAGCATG[A/C]AAAGAAGCTGAAACC | 7874 |
rs568518496 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8955373 | CCTCGGCCTCCCAAA[A/G]TGCTGGGATTACAGG | 7874 |
rs568521019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8944090 | ACTGGGACAATATCC[A/G]TAATACATCAAGTAT | 7874 |
rs568574007 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8930577 | TACATACAAACTTTC[A/G]CTGTTTCGAAACACT | 7874 |
rs568581031 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8912859 | AAAAATAAAAAAAAA[A/T]TTAAAAAGTTTGAAA | 7874 |
rs568603280 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8944705 | AGACACAGACCACCA[C/T]TCAGGTTTTAATCCC | 7874 |
rs568643558 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8947125 | GTAAGATTGGTTTTT[C/T]CATATTTTAATTAAA | 7874 |
rs568653919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8949146 | ACTTTAAATGGGTGA[A/G]TTGTGGTATGTGAAT | 7874 |
rs568657527 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8907429 | CACTCTCCCTTAAAC[C/G]TGAAGGCTGAATGAC | 7874 |
rs568679557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8939521 | GTTTCTATTTATTTC[C/T]ACTTTTGAGTTCTGA | 7874 |
rs568692680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8907945 | AGAGACAACAAAATA[C/T]TGGAAAATCCTATTT | 7874 |
rs568791167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8935413 | ATGGGGTTTCACCAC[A/G]TTGGCCAGGCTGGTC | 7874 |
rs568802738 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8905402 | CACTAGAAGGCAGCG[C/T]TGTTCTAAAATGTGT | 7874 |
rs568834966 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | USP7 | GRCh38.p7 | 16:8945903 | AAAAAAAGTAAAAAT[A/T]AAAAAAAACAACAGC | 7874 |
rs568836216 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950212 | GTGGCTAGTGGCTGC[C/G]ACAGTGGACAGCGAA | 7874 |
rs568849565 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8918407 | AGTAAGTTGCATTGA[C/G]TTTTCAACTCAGTTT | 7874 |
rs568883924 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8933664 | TACAATGTTGCCCAG[C/G]TTGGTCTTGAACTGG | 7874 |
rs568916980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8905728 | TCCTTTAGTTATCAA[A/G]CTAAATGAGCTGTTT | 7874 |
rs568919210 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8935655 | TACCATCCCATAATA[C/T]GCATATCCCACTCAG | 7874 |
rs569014428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8918770 | GCCAAGGTCACACCA[C/T]TGCACTCCAGCCTGG | 7874 |
rs569023625 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8897728 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 7874 |
rs569024706 | snp | C/G/T | 0.00287383 | 0.0377976 | utr-variant-5-prime, intron-variant | USP7 | GRCh38.p7 | 16:8936722 | CTCAGCATTCTTTTT[C/G/T]ATTTTTTAAAGCATC | 7874 |
rs569094014 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8919907 | AAACACTCAAATACA[A/C]CTAACGGCCTTGTCA | 7874 |
rs569161627 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8916188 | GTGACTCAGGACCAA[C/T]GGGACAGCCAACAAA | 7874 |
rs569163943 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8910594 | TCCCCCTCTCCCTCC[C/G]CATTCAATTATCCTA | 7874 |
rs569171261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961090 | TTACCTTTCTAATAC[A/G]AACTGTAATATGAAA | 7874 |
rs569182269 | in-del | -/T | 0.00120337 | 0.0244997 | intron-variant | USP7 | GRCh38.p7 | 16:8904788 | CTACTACTAAAAAAA[-/T]AAAATAAAATAAAAA | 7874 |
rs569188556 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937282 | AGGCAGGGTGGCTCA[A/C]GCCTGTAATCCCAAC | 7874 |
rs569195756 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8945506 | CCTATAAACCAACAG[A/C]CACCTTGAACATTTC | 7874 |
rs569215152 | in-del | -/A | 0.0142044 | 0.0830689 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937214 | CTCTGTCTTTTTTTA[-/A]AAAAAAAAAGGATTA | 7874 |
rs569249978 | snp | C/T | 1.6777e-05 | 0.00289624 | intron-variant | USP7 | GRCh38.p7 | 16:8920309 | CTAAAGCTTCTTTCA[C/T]TGCAGCACAAAAGAC | 7874 |
rs569299125 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937498 | AGTGAACTGAGATCA[C/T]GCCATTGCACTCCAG | 7874 |
rs569308458 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8924783 | GTAGTATTGAAATAT[C/G]AAAAGCATGTGTGAC | 7874 |
rs569316608 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8933922 | ACCACGCCCAGCTAA[-/T]TTTTTTTTATTTTTA | 7874 |
rs569320407 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8946927 | TCCATATTTTCCAAA[C/T]GGCCAATAAATGCAA | 7874 |
rs569326314 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8892265 | ACTCCTCTTTCTGGG[A/G]GAGGAAGGAGGGAAG | 7874 |
rs569330352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8925039 | ACGTCTAGAATGGCG[C/T]GGTGGAATAAGTTTT | 7874 |
rs569359426 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961376 | ACATGGCTGTAATCC[C/T]AGCTACTTGGGAGGC | 7874 |
rs569415694 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8926206 | AGGTCGGCCGGGCGC[A/G]GTGGTTCGCGCCTGT | 7874 |
rs569437358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8952762 | CAAACCACAGACCCT[A/G]AACCTCTAGTCACAG | 7874 |
rs569476656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8946574 | ATATAAACAACAGTT[C/T]ACAAAACTCAACAGC | 7874 |
rs569479668 | snp | A/C | 0.0130921 | 0.0798413 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956769 | CTTCGTATTAAAAAA[A/C]CAAAAACAAAAAAAA | 7874 |
rs569483288 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8911541 | ACAACACTGAAAACA[C/G]CGCTGTCACGCTCCG | 7874 |
rs569620941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8930683 | ATATAAAATCTCTTA[C/T]GTAGGCCAGACATGG | 7874 |
rs569637852 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8941306 | CCTTTCTAAGCTGCT[A/G]CCATTAGCTAGGATT | 7874 |
rs569653268 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8930930 | GCCAAGATCATGCCA[C/G]TGCACTCCAGCCTGG | 7874 |
rs569654439 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8922360 | GGGTGTGGTGGCACA[C/T]GCCTATAGTCCCAGC | 7874 |
rs569659604 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8934876 | CCCAGGGGCAGGAGA[C/T]CCCGTTTTTAAAAGC | 7874 |
rs569664897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8940505 | GAGGGCAGGGGTTAC[C/T]TTGGGACCAGGCAAC | 7874 |
rs569681730 | snp | A/G | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964170 | CGGTGACTTAGCCCT[A/G]CGGAGGTGAACCGGA | 7874 |
rs569709249 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8939287 | CTCCCCCATTATCCC[C/T]GGCAACCCTCATATG | 7874 |
rs569730579 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893421 | TGGCTGACGAGGTGA[A/G]ACAAGTTTATTAAAA | 7874 |
rs569756176 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8955576 | CCGGGCATGGCGGCG[C/T]GCCCCTGTAGTCCTG | 7874 |
rs569759702 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8958531 | GAGGCTACCACCACA[G/T]TTCCAGCATGAGGCA | 7874 |
rs569798054 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8949039 | AGTGGTGACTGCTAA[C/T]GGGTACAGGATTTCC | 7874 |
rs569808162 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894319 | CCTGAGTCTCAATCA[C/T]CCTGCACACATATCC | 7874 |
rs569827713 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8949480 | ACATGGCAATTCCAA[C/T]ACAATGGACATACCC | 7874 |
rs569828345 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8940897 | TGGAATATATACAGT[C/G]TCCAGAACCTGGAGG | 7874 |
rs569831559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8954519 | CCTGTTAACCGTAAC[C/T]CAAAAAGTCAAATCC | 7874 |
rs569840378 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8935769 | AAACACCAAGTAGGC[A/T]CCCTGGCTAGTTCCA | 7874 |
rs569888025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8913057 | TGAGAAGGAAAAAAC[C/T]TTAAAAGCACATGGG | 7874 |
rs569891785 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8955242 | ATTAATCTGTTTGCA[-/T]TTCATTTCTACATGA | 7874 |
rs569908846 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8944793 | ATCTTTTGAAAAACT[A/T]GCGTCAAAGGTATTT | 7874 |
rs569919908 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8916339 | AAGTAATTCTTACCA[C/G]CCTTTATAACTAGAC | 7874 |
rs569940711 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8936094 | ACCCTGGTGTGTTGA[A/G]ACTAAGAGTCCATGT | 7874 |
rs569967898 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8913376 | GAGGAGAGAAGAGGG[A/T]AGACAGGAGAGAAGA | 7874 |
rs570008066 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8954999 | CAGTAACAGCAATTG[C/T]TGTTTCACACAACAT | 7874 |
rs570044755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8959482 | TGGAGCCTGGGGAAT[C/T]GCTTTGAATCATTAA | 7874 |
rs570066889 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | USP7 | GRCh38.p7 | 16:8943798 | AAAAACCCATTCCCC[A/G]AGAAAATGAGCATTC | 7874 |
rs570083003 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964959 | GTCCTGTCTCATTCA[A/G]TCATTGACAGACTGA | 7874 |
rs570110655 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8899429 | CAGGTTCTTTTCTGA[C/T]GGCGATTATTCTAGC | 7874 |
rs570139321 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8931960 | ATGTGCTTTTTAACA[G/T]CCAGGTAGTTGTGTG | 7874 |
rs570153025 | snp | A/G | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8909405 | CATTTAAGAGGACAG[A/G]GCTATCTCAGGAAAG | 7874 |
rs570162473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8913642 | CATCTCAGCCGACCC[A/G]CACTAAATGATTCCT | 7874 |
rs570192664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8908918 | ACACAACTGATGAGT[C/T]GGCAGGATTATAAGC | 7874 |
rs570235729 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937702 | AGGCTACAAAAAAAA[C/T]AGAAAGGGAAAAATG | 7874 |
rs570252383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8898808 | AACTAAGTCCCACTC[A/G]CTGTCACACTTGAAT | 7874 |
rs570260515 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8955482 | AATCCCAGCACTTTG[C/G]GAGGCCGAGTGAGGC | 7874 |
rs570286105 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8910008 | AGTACATTTGGAGCT[A/G]ACAGCTGACTACAAA | 7874 |
rs570323375 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960154 | TAAATAATACACTGC[A/C]AAGCAACCTTATTCC | 7874 |
rs570325903 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8911606 | GACAAATGAGAGCCC[A/C]GTGATGGGCCCAGCT | 7874 |
rs570362104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8900022 | CCCTTAGGTAACAGC[A/G]CCTGCTCTCCTCTAC | 7874 |
rs570405161 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956784 | ACAAAAACAAAAAAA[A/C]AAAAACACTGAATTT | 7874 |
rs570405442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962476 | AGAAAACCGAGTTAC[C/T]TTTCGAGTCAGGTTT | 7874 |
rs570405949 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8911501 | AGCTCGTCCTGCTCC[A/G/T]GTCATGAAGGAAAAA | 7874 |
rs570441787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8915587 | AATATATACAGTAAT[C/T]TTATAATTGACTAGA | 7874 |
rs570443329 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962196 | TTGCTAAAAGCAAAA[C/G]TAAAGCATTCCACGC | 7874 |
rs570516395 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957150 | AGAAGTAGACCTGCT[A/T]CTCTTCAAAAATTTC | 7874 |
rs570547527 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892397 | GGAAGTCACTCCAAG[C/G]TACACACTGGCCCAA | 7874 |
rs570550779 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | USP7 | GRCh38.p7 | 16:8905853 | GGATGCAGCCACATT[A/C]AACAGTGATGAACGC | 7874 |
rs570552810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8911546 | ACTGAAAACAGCGCT[A/G]TCACGCTCCGGACAC | 7874 |
rs570556294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8901337 | AAAAAAAAAAACAGT[A/G]AGCTGAATAGCTCAA | 7874 |
rs570589218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8911261 | CGGGGTGGGGTGGAA[A/G]TTGGTCCTGACATCT | 7874 |
rs570614430 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8933982 | GGCTGGTCTCAAACT[A/C]ATGACCTCAAGTGAT | 7874 |
rs570668454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8955654 | GAGGTTGCAGTGAGC[C/T]GAGATCACACCACTG | 7874 |
rs570716896 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956938 | AGACAAGTCGACGCT[A/C]TCTCTCAGGGTGCCT | 7874 |
rs570722698 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8925173 | GGAGGTTCGCCGAGG[C/T]TGTTTTACAAAGTGA | 7874 |
rs570727945 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8929646 | GCATACTGCAATTAC[G/T]GGCTGCTCCCTACTC | 7874 |
rs570794506 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8896889 | CCACTGAGTCTGGGA[A/G]TGACGCGCATGGATC | 7874 |
rs570797612 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8953038 | GACGGGGTTTCACCA[C/T]GTTGGTCAGGCTGGT | 7874 |
rs570801046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8907362 | GACCACGGTAAAGAC[C/T]GTGAATGGGTGACCA | 7874 |
rs570863576 | snp | A/T | 0.000363714 | 0.0134805 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8894599 | ATACTCGTCTTCATT[A/T]ATGTACTGGTGTCGG | 7874 |
rs570874914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8916727 | AGATTTACTGCTGGG[A/G]AAGTGGTGTTTCCAA | 7874 |
rs570916898 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8959405 | TTACTAGTATCGATC[A/T]TTTCATTACAGAGAA | 7874 |
rs570970314 | snp | A/G | 1.71217e-05 | 0.00292584 | intron-variant | USP7 | GRCh38.p7 | 16:8917006 | AAGCAGAATGGCAAA[A/G]GCAGATGTCTAATAC | 7874 |
rs570993771 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8949420 | GTCCCTGAACTTTAC[A/C]ACCTCAAAGTCTAGT | 7874 |
rs571001866 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8920949 | GAACTCCCTTTGAAT[G/T]TCTGACTAAAAAGTG | 7874 |
rs571038449 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8912106 | AGGAATATCTAACAC[A/C]CAGCAAGATAAAAAC | 7874 |
rs571106699 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8943613 | TTCCTCTGCTGGATT[A/T]ACGGTGAAAAGCAAT | 7874 |
rs571126196 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8954883 | GAGAATGGTGTGAAC[C/T]CGGGAGGCAGAGGTT | 7874 |
rs571207025 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8918352 | TCATCTATATTAGAT[G/T]TAATGTATGTCTATT | 7874 |
rs571232209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8954643 | TTTACTAACTAAATA[C/T]GAAGGTATGTATTCA | 7874 |
rs571241768 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8927495 | CACAAATTAGTTTCA[C/T]GGAGAACAACATTCT | 7874 |
rs571248184 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8939281 | TGCGTGCTCCCCCAT[G/T]ATCCCCGGCAACCCT | 7874 |
rs571275520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8912013 | AAACCTGTTCTCCCA[C/T]CTAGCAAGGCTTAAA | 7874 |
rs571289735 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961562 | TTTTCCCAAAGATAC[A/G]GGTCTGTAACACACA | 7874 |
rs571296141 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8922656 | AGGTTGACAAAGTGG[G/T]CCGTACTCCCAGAAT | 7874 |
rs571385476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8938870 | ATTTAAACTATATAG[A/G]AAGATGTGTGAAGAT | 7874 |
rs571402732 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8941169 | CCCCACCACCAAATT[A/G]CTTCCCAGCCCTCAC | 7874 |
rs571412425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8928219 | TACTAAGAAGTCTTC[C/T]GTGCAAATCAGTCAA | 7874 |
rs571426302 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8941091 | CCACACTGCCCATGT[A/T]TGCCAAGGAGCTGCT | 7874 |
rs571428239 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8945868 | CCAGCCTGGGCAACA[C/T]AGCGAGACCCCACTT | 7874 |
rs571468317 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950695 | AAGCTGTATGTGCCT[C/G]GCTGCCCTGCATCCT | 7874 |
rs571488038 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8923914 | TGCTCAGAGGCAAGA[A/C]AAGGGCTACAACAGT | 7874 |
rs571491552 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8919217 | TGAAGCAATCTGACT[C/T]AAGGTCAGCCTTAAG | 7874 |
rs571545677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8914199 | GTAAGAACAACCTCA[C/T]TGATCTTCAAGGAAA | 7874 |
rs571552295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8904967 | AGAGCAAGACTCCGT[C/T]TCAAAAAAATAAAAT | 7874 |
rs571557301 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8896501 | AAGTAGTGAGAATCA[C/T]GCCCATCTCTCTGAA | 7874 |
rs571561072 | snp | A/T | | | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962331 | AATGGGTCGTGAGAA[A/T]AAGTGCCTTCCAACG | 7874 |
rs571611786 | snp | A/T | 0.00795532 | 0.062565 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937215 | CTCTGTCTTTTTTTA[A/T]AAAAAAAAGGATTAA | 7874 |
rs571686974 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8900137 | GCTTTCGTGTGCCAT[C/T]GAGCCACTTTCAGAC | 7874 |
rs571716010 | in-del | -/TG | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8921592 | GACCTCTGCTTCTAC[-/TG]CCGATATAGGGGTCA | 7874 |
rs571717844 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8932985 | TTCGCTCGTTGCCCA[C/G]GCTGGAGTTCAGTGG | 7874 |
rs571722481 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8951780 | ATGGTTTGCTTTAGG[A/C]ATGATTCATTCAGCT | 7874 |
rs571737431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8929226 | TGCACTCACTCAACC[A/G]CTTTCGGCATCTCAG | 7874 |
rs571790874 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892473 | ACGGTGCAAGGACCA[C/T]GCCCACGATAGCGCC | 7874 |
rs571812792 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8925296 | AACACACACAAAACA[C/T]AGGCCTCAACAAAAT | 7874 |
rs571832668 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8946505 | ACACACGAGCTACAG[A/G]CCAGCAGAAAATATC | 7874 |
rs571864338 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8919819 | CAAGCGGGACCAGTG[A/C]TGGGGGAGACACCTA | 7874 |
rs571865242 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8948071 | GCATGCCCTGCAGAC[A/G]TCAGTCAGCTCCAGC | 7874 |
rs571870878 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | USP7 | GRCh38.p7 | 16:8927080 | AGCACTCTGGGAGGC[C/T]GGGGTGGGCGAGGCG | 7874 |
rs571883925 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8948231 | CACCAGCCCAGGCTG[C/G]AGAATGAGTGGCACC | 7874 |
rs571894823 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8952288 | TAACCACTACTTTAT[G/T]ACCAATAGCACTTAC | 7874 |
rs571957363 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891914 | TCCACACCCCACAGA[A/G]GGAGAGGACACAATA | 7874 |
rs572027044 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960281 | GTTGCAACCCCAGCA[A/C]ACTGCATCAGGCCCC | 7874 |
rs572040457 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957350 | ACTCTGTCATGGTAC[A/G]TGGCAAGAAATATGT | 7874 |
rs572042602 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8935640 | AGGAAATAAAGCAAT[C/T]ACCATCCCATAATAC | 7874 |
rs572051575 | snp | A/C/G | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8892952 | ACTAGACACGCAGCT[A/C/G]GCATTAGCTCCAAAA | 7874 |
rs572071627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8896191 | ATCAGAAACAGAGAC[C/T]GGAGGCAAGGCACGG | 7874 |
rs572074613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8920626 | ACAGTGGTCTCACAA[C/T]AAATACAGCAAATGC | 7874 |
rs572090440 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962268 | GAACTCGTCACGTAG[A/G]TAAGAAAACTTTTTA | 7874 |
rs572105848 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8952931 | AACCTCCGCTTCCTG[G/T]GTTCAAGCGATTCTC | 7874 |
rs572107757 | in-del | -/G | 0.0107246 | 0.0724382 | intron-variant | USP7 | GRCh38.p7 | 16:8926500 | AAAAAATTCAAGATA[-/G]GAGGGCCAAAAAAAA | 7874 |
rs572139657 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937503 | ACTGAGATCACGCCA[C/T]TGCACTCCAGCCTGG | 7874 |
rs572149227 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892460 | CAAGGCCGATGGGAC[A/G]GTGCAAGGACCACGC | 7874 |
rs572152960 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8944212 | AAACAAAAGCAAAAA[G/T]ACGCAGAGCAACAGA | 7874 |
rs572165287 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8963087 | GGAGGCCAGGCCGAG[C/G]CCCGGCGGCCGCCCG | 7874 |
rs572210658 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8896697 | TGCGCCTTTTTACTA[C/T]AGCTAATGTTATCAG | 7874 |
rs572227245 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8914587 | CAAACTATGACTACT[A/C]CCAGCGTGGATGTAT | 7874 |
rs572284667 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8892844 | TATACAGGAAGAGTT[C/G]GTGTACACTGCTCCC | 7874 |
rs572291168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8916845 | TACAACAAAGTGTCT[A/G]TTTCCAAAGAGATAA | 7874 |
rs572309584 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8939703 | CATGTACATTGCTCG[A/T]GCACTTTTTCTCATG | 7874 |
rs572327441 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964275 | CGGCAGCCGGGGTTC[A/C]GGTCCCAGCCTAGCG | 7874 |
rs572327499 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8958101 | CACAAATAAATTTAA[C/T]AAAAAAGGAAACTGA | 7874 |
rs572357776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8934527 | GATTAATTGCAGTGT[A/G]ATGACTAAAGAAAGC | 7874 |
rs572423961 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8932897 | TACTAACTGAATAGG[-/A]AAAAAAAAACCAATG | 7874 |
rs572451034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8939140 | GTACTTACGTGTATT[C/T]AGTTCTCTACAATTT | 7874 |
rs572456136 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8912609 | ATTATCAACTATACT[A/T]AAGTCCAAAGGAGAA | 7874 |
rs572486283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8907046 | AATTAACAGAGGCAG[A/G]AAGGCAAGTTAGACG | 7874 |
rs572528408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8902839 | GTTGCAGTGAGCCAA[A/G]ATCGCGCCACTGGGC | 7874 |
rs572528812 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8910244 | TCCAAGCGGGGGCTG[A/G]CCACCTGGTCGCCCA | 7874 |
rs572549936 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8946003 | CGGACAGGGGAGAAT[G/T]GAAGAGTCCAGAAAC | 7874 |
rs572553030 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP7 | GRCh38.p7 | 16:8897790 | TGTAATCCTAGCTAC[C/T]TGGGGGGCTGAGGTG | 7874 |
rs572554272 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8912866 | AAAAAAAATTTAAAA[A/T]GTTTGAAAATGAAAC | 7874 |
rs572618386 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8922115 | ACTCATCAGATCACA[A/T]CATAATGTGAACAGA | 7874 |
rs572647587 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8954324 | GGAGATTGAGCCTTA[C/G]ATACCTTTTTAAGAA | 7874 |
rs572667488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8931035 | AATCAGCGTAAAGAA[C/T]CTTTATCTAATCATG | 7874 |
rs572669332 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8926253 | GAGGCAGAGGCGGGC[A/G]GATAACCTGAGGTCA | 7874 |
rs572706472 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8930767 | TGAGGCCAGGAGTTC[A/G]AGACCAGGCTGGCCA | 7874 |
rs572708247 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8936384 | CTCCTCTCCCCACAA[A/T]GAACTCATTTAAATA | 7874 |
rs572722094 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8928445 | CAACCCTGAGACATA[C/T]GACAGTAAATAAAGC | 7874 |
rs572734851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8909716 | GCGGATCACAAGGTC[A/G]GGGGTTTGAGACCTG | 7874 |
rs572754031 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8941652 | GTAGCCTTGCTTGGT[A/T]CCAGGAAAGACAAAG | 7874 |
rs572758260 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8922088 | TCGGACTAAAACAAA[C/G]CTAGCCCAAATACTC | 7874 |
rs572782888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8926621 | CTTTGCCCAAGAAAA[C/T]AGTTAACAGTACACT | 7874 |
rs572789283 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8920070 | GGGTATTTATGTACC[A/G]GTCTTAGCTCCTCTA | 7874 |
rs572794796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8941268 | GGAAAAATTAACTAT[A/G]CTCAAACATAACCCT | 7874 |
rs572834335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961130 | CATTTTATGAGAAAA[A/G]AAAGTAGCCTTGAAA | 7874 |
rs572840700 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8895296 | ATCCAGCCAGAGTGA[A/T]GGGCACTCATGGGAG | 7874 |
rs572877263 | in-del | -/T | 0.00676609 | 0.0577691 | intron-variant | USP7 | GRCh38.p7 | 16:8941128 | TTCACATGGGGCCCA[-/T]GCCCCATGCCCATGA | 7874 |
rs572913429 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8936870 | ACTTTGGTTAACAAC[A/C]TACCAATGCCAGTTC | 7874 |
rs572941350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8910240 | TTCATCCAAGCGGGG[A/G]CTGGCCACCTGGTCG | 7874 |
rs572973094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960454 | CAAGAATGTGAGGCC[A/G]GAGAGCAAACTCACA | 7874 |
rs572975474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8910993 | GGTAAATGTGCTGTT[A/G]GCACCTTTGCTCATT | 7874 |
rs573059239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8923747 | TGGAGAGACCTTGGA[A/G]AGAAGGAACGACATG | 7874 |
rs573067960 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8928306 | TGCCCTAGTCTGAAA[A/T]GGACACTCAACACTC | 7874 |
rs573076567 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8958468 | GTCCTGTGGGCAGCA[C/G]CTTTCATAAAGTGTG | 7874 |
rs573086123 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8955597 | TGTAGTCCTGGCTAC[G/T]TGGGAGGCTGAGGCA | 7874 |
rs573091771 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8955997 | TTGCAGCCCCACCCT[C/G]GGATGGGACCATGTT | 7874 |
rs573104975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8932660 | CTCTGAAATGTCTTT[C/T]ATCCACATTCATTTT | 7874 |
rs573112990 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960406 | TGAATATACAAGGAC[A/T]GTGCAGAGTTCACTC | 7874 |
rs573124697 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8952524 | GGGTCCTAGAGCCAC[C/G]CCATTCCTGGGCTCC | 7874 |
rs573179511 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8928668 | GGTCTTTCAACGGCA[A/T]CCACAGTTCCAAACC | 7874 |
rs573187167 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8919456 | ATGCCTCATGGTAGA[C/G]TTTGGTTACATAATT | 7874 |
rs573189936 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8925485 | TGATTTTATGTATAC[-/A]AAAATCAATACATAT | 7874 |
rs573207420 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891751 | CGCGCCTGGCTGCTC[G/T]TCTCATTTTGAAACA | 7874 |
rs573218649 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8933732 | TGGGATTACAGGCAT[G/T]TGCCACCCTGCCTGG | 7874 |
rs573222099 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8924265 | GACTCCTGCGAAGGC[A/T]CAGTCCTCCCACACC | 7874 |
rs573266174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8919952 | TCGCTCACCATGTTA[A/G]TTGTCGGTGATGCTC | 7874 |
rs573281513 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8951981 | GGAACCACACCACAA[C/G]GTTCAGACTGGGAAG | 7874 |
rs573344554 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938063 | CAGAATATCCTCCCT[A/G]TGTCACCAGACCAGG | 7874 |
rs573355981 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8947023 | ATTAAGTTACCACTT[C/G]TTTTGCTTTGCTGTA | 7874 |
rs573376749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8917614 | AAACTCCTGACCTCA[A/G]GGGATCTGCCCACCT | 7874 |
rs573420553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8906334 | GTTAGGGGTCCCTGA[C/T]AAGGTTCCGAGTAGG | 7874 |
rs573444762 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8901530 | TAGTTCTGAGACCTG[C/G]ACTGACTGGCTGGAA | 7874 |
rs573487992 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8913072 | CTTAAAAGCACATGG[G/T]GGGCTGGGCACGGTG | 7874 |
rs573516054 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8919663 | ATTCTCAGAATTAAC[C/T]GTGTCTCGTACCTTC | 7874 |
rs573530610 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8905942 | CCTTGGCAGGAGCTC[A/G]GTGCTGGCCCTGTGG | 7874 |
rs573537934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961837 | ATCACACATAACAGG[C/T]GCTCTTAGTTGCTGC | 7874 |
rs573549095 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8940054 | AGTGAGCTGAGATCA[C/T]GCCACTGAACTCCAG | 7874 |
rs573587604 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | USP7 | GRCh38.p7 | 16:8926244 | GCACTTTGGGAGGCA[C/G]AGGCGGGCGGATAAC | 7874 |
rs573650319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8954246 | GAGGGAAGACACGTG[C/T]CCCCTGCGGTGCCAC | 7874 |
rs573657048 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8931545 | AATTATGTAAAGATC[C/G/T]GGGAAAGTGTTTAGG | 7874 |
rs573659101 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8913985 | TCAAGCAATCCTCCC[A/G]ACTCAGCCTCCCAAA | 7874 |
rs573684725 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8917402 | CCACCCACGTGACAC[A/G/T]AAGTCTCACTCTGTT | 7874 |
rs573687132 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8953543 | AGAGGGAAGACACGT[C/G]CCCCATGCGGCGCCA | 7874 |
rs573742880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8931150 | AAATGGTATACATTA[A/G]AACAAATATTTTAAA | 7874 |
rs573763134 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8949123 | GAATACTAAAAACCA[C/G]TGAACCCACTTTAAA | 7874 |
rs573771847 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8919549 | CACACACACAAGAAG[A/G]AACAGAAGTGTGTAT | 7874 |
rs573813404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8903710 | CTGTCTCTACTAAAA[A/G]TACAAAATTAGCTGG | 7874 |
rs573818434 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8917479 | CGCCTCCTGGGTTCA[C/G]GCAATTCTCCTGCCT | 7874 |
rs573865323 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950326 | AAAAAAGATGGGACC[C/G]AGTGCTCTCTGATAA | 7874 |
rs573867625 | snp | A/C | 0.225005 | 0.248747 | intron-variant | USP7 | GRCh38.p7 | 16:8954016 | GAAGACACGTGCCCC[A/C]TGCGGCGCCACTGGA | 7874 |
rs573943004 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964465 | TCTCACTGTCAGCCT[A/G]ATCTGGCAAAGTTTG | 7874 |
rs573999976 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8910235 | TTCCCTTCATCCAAG[C/T]GGGGGCTGGCCACCT | 7874 |
rs574045418 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8954699 | AGCAATTGCAGGCCG[C/G]GCACGGTGGACTCAC | 7874 |
rs574072078 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8927194 | AGGCGTGGTGGCAAG[A/C/T]GCCTGTAGTCCCAGC | 7874 |
rs574078819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8959520 | CGTGCTCACATCAGA[A/G]TGAGATGCTAGGTTT | 7874 |
rs574086465 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8959055 | AAAGCCCTACCACCA[A/C]GGCAACACCATGTGC | 7874 |
rs574160532 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, missense | USP7 | GRCh38.p7 | 16:8894454 | GTGGAGAGAGAGGAG[C/G]TGGCACTTGACCCTG | 7874 |
rs574193894 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956712 | AGGTTGCAGTGAGCC[A/G]AGATCGTCCCACTGC | 7874 |
rs574226138 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8898970 | AGAGTAATGTGGTCA[A/G]GATGTGAGTGGTGAC | 7874 |
rs574273858 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8939913 | AACCATCCTGGCTAA[C/T]ACGGTGAAACCCCGA | 7874 |
rs574282596 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8918101 | AGCCATGGAGCACCA[C/T]TTCTTAACTTACCAT | 7874 |
rs574301072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8894726 | AGCCTAGGCCGCTAC[A/G]CTAGGCAAGGCTTGA | 7874 |
rs574307913 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8952586 | TCTGGCACTGATGAC[G/T]GTGAGTACACTAGGC | 7874 |
rs574310374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8928839 | AAAGGAAGGGGACTT[C/T]ACCCATATTGTCCCC | 7874 |
rs574382390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8947631 | GGGATTACAGGTGTG[C/T]GCTTATTTTTCAATC | 7874 |
rs574398043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8918486 | TAAATACCTTCACAA[A/G]GTGATTTCTAACACA | 7874 |
rs574402629 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962250 | TTTGACTCCCGACAG[C/G]CTGAACTCGTCACGT | 7874 |
rs574420650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8952881 | TCTTGTTGTCGCCCA[A/G]GCTAGAGTGCACTGG | 7874 |
rs574454495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8896121 | TGGGATTATAGGTGT[A/G]AGCCACCATGCCCAG | 7874 |
rs574492077 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8895831 | AAGAAATAAAGTTAC[C/G]ACGATATGTTTTTTT | 7874 |
rs574496598 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8948184 | TTCCGCTCCCCTGAT[G/T]GAACCCTCAACTGAC | 7874 |
rs574504591 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892433 | AGGAAACCGTGCCAC[A/G]GAGCTGGAAGGCAAG | 7874 |
rs574505271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8900888 | GGCCCTGAGTTAGCT[A/G]GTAGACCTAACACTG | 7874 |
rs574510268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961749 | TTATGTTTTAGATGG[A/G]CTGCAAAATACAGCA | 7874 |
rs574512159 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8945503 | CAACCTATAAACCAA[A/C]AGACACCTTGAACAT | 7874 |
rs574545333 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8925269 | TAAAATTCCACTCCT[A/G/T]GAAGTTACCATAACA | 7874 |
rs574591543 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, nc-transcript-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8892078 | ACGCGGCAGATGACG[A/G]AAACATTACAACACG | 7874 |
rs574615985 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8901433 | GAGGCTATTACCGCT[C/G]AGTTTCCAAACATCA | 7874 |
rs574639246 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8949766 | TTACGCAGAGACACC[G/T]TATCACTTCATCTCT | 7874 |
rs574639472 | in-del | -/GGCC | 0.00636936 | 0.0560724 | intron-variant | USP7 | GRCh38.p7 | 16:8941122 | GCCCAATTCACATGG[-/GGCC]CATGCCCCATGCCCA | 7874 |
rs574685149 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8920045 | AGTAACAACGGAGCA[C/T]CTCTGCTCTGGGTAT | 7874 |
rs574703778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8896666 | TCCTTCCTCTGTTTG[A/G]CTTTTCTATGGGAAC | 7874 |
rs574753852 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8916421 | TTCTGAATTAGGTCT[C/G]AGGTTTTACTTGGTA | 7874 |
rs574759227 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8911887 | AACCTTCAGAGCTCA[C/G]GACAGGCTGGGAAGT | 7874 |
rs574772659 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8897692 | TATAGTGAGACCCTG[G/T]CTCTACAAAAAAAAA | 7874 |
rs574797966 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8906989 | TTAACTGGCTCTACA[A/C]ATTTTGATTTACTTG | 7874 |
rs574802972 | in-del | -/A/AA | 0.494815 | 0.0506538 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938710 | GCAAGACTCCGTCTC[-/A/AA]AAAAAAAAAAAAATT | 7874 |
rs574867544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8916777 | AAGCAGTACAGGTTC[C/T]TGTGTTGAAAAGTAA | 7874 |
rs574880037 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8912168 | CAAGCATGTGAACCA[C/G]TGCAGTGGCTCAGTG | 7874 |
rs574909470 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8922514 | GGGGATCTGACAGAA[A/C]AGCCAGAGTCAGTTC | 7874 |
rs574950719 | snp | C/G | 1.65425e-05 | 0.00287593 | intron-variant | USP7 | GRCh38.p7 | 16:8904574 | ACTTCACCTGCAGGA[C/G]AAAGGCATCCTCTTT | 7874 |
rs574968915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8934222 | CTAAAATCAGGATCA[C/T]ATGTAAGTGTAAGCA | 7874 |
rs574999138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962636 | ACAGCGCCCGGGTCA[A/G]AACTCTGGGCCAGTC | 7874 |
rs575065598 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8963029 | GCGGCCGCCCCTCGC[A/C]CGCGGACCCGGCATG | 7874 |
rs575099568 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8925401 | TGCAGGACCTAAAAA[C/G]CTGAAAGAAACAAGG | 7874 |
rs575115465 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8913507 | CGAGCAAGAAGACGG[C/T]AGAACGTCTAACAGA | 7874 |
rs575136106 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP7 | GRCh38.p7 | 16:8945211 | CCTGGGCAACAAGAG[C/T]GAAATTCCATCTTCA | 7874 |
rs575176517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8900254 | CGATTTCATAAATCT[C/T]AGGGGAAGGAAGCAA | 7874 |
rs575192061 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8899895 | TTCCCCTTTGAGGGG[A/G]CCAGGCATCTGCCTG | 7874 |
rs575206405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8953281 | GTGTTCAGGGCTCCT[C/T]CACTTTCTGAGGCAG | 7874 |
rs575206949 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961023 | TAGTAACTAAAACCT[C/G]TGCCATCCAATTTGA | 7874 |
rs575231879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8930720 | ATGCCTGTAATCCTA[A/G]CATTTTGAGAGGCCA | 7874 |
rs575271490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8923058 | AAAAATATACTTTTC[C/T]AGCTTGGATATTATA | 7874 |
rs575277868 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8940727 | GAGGCTGTGGAGTGA[C/G]ATCAATCCCCTCTGC | 7874 |
rs575306407 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8932174 | TCTCAAAACATTCAA[A/C]ATACCAAGAAACAGG | 7874 |
rs575307757 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8919346 | CACATTCGCACAGCC[C/T]TCGAAGCACCTGCCT | 7874 |
rs575339461 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8913885 | CCTCAAGTAGCTGGG[A/C]CTACAGGTGCATGCC | 7874 |
rs575344468 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8923999 | CCTGGACACCCTAGG[G/T]GGAATAATTTTTTTT | 7874 |
rs575344806 | snp | A/C/T | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8918923 | AGCCATCTGAGGAGA[A/C/T]AGGGCCAGGGGAGGG | 7874 |
rs575366265 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964917 | GGGCCTCCCTATTCC[A/G]GGAGACATTTGGTGA | 7874 |
rs575387932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8941263 | TAAGTGGAAAAATTA[A/G]CTATGCTCAAACATA | 7874 |
rs575435232 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8943872 | CAACTTTAAACATAA[C/G]TTTAATTTTTCACAG | 7874 |
rs575473006 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8927840 | GAACCTATCTCAAAA[C/T]AAAATAAAATAAAAC | 7874 |
rs575487891 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8959820 | CCACCACCACCCCCG[G/T]AACAAAAAACACAGA | 7874 |
rs575557209 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8936291 | TCACATGGCGCCCTA[C/G]AGCCCATCTCACCCC | 7874 |
rs575558396 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8925636 | GCCCAGCCCCGCAGA[A/G]GCCACCGCGCATCCG | 7874 |
rs575613920 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8895262 | AAGCCTATTTTTGCT[A/T]AAAAAACGCCACACC | 7874 |
rs575619047 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8914655 | CTGGACATGGCAGCT[C/G]ATGTCTAATTCCAGT | 7874 |
rs575628420 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8928248 | AAGTCGCTGATAGTT[G/T]GGCTACAGACCAAAC | 7874 |
rs575643543 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891736 | CACAGCACGAGCCAC[C/T]GCGCCTGGCTGCTCT | 7874 |
rs575666728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8925369 | AACTGCACAGAAGCA[A/G]CCAAATGGAAAATCA | 7874 |
rs575669273 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960954 | CTGGATAATGAAATT[C/G]AAACAGAGGCCCAGT | 7874 |
rs575695770 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8921682 | TAGGATGCCCTCCAG[C/G]ACATGCTGGGGGAAA | 7874 |
rs575711199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962695 | CAGGTATTTTCGAAC[A/G]TAAGCCCGACGCTAG | 7874 |
rs575722911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8955563 | TACAAAAAATTAGCC[A/G]GGCATGGCGGCGCGC | 7874 |
rs575734968 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8921101 | AAAATCAAAAAGTTA[A/C]GGGAACAACAAGCAG | 7874 |
rs575753672 | snp | A/C/G | 0.00239401 | 0.0345304 | intron-variant | USP7 | GRCh38.p7 | 16:8941704 | GAGGAGTGAGGGGAC[A/C/G]GGCAGAGCCAGGATC | 7874 |
rs575777339 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8915094 | CACCAGAGCTGGGTG[C/G]AGGTAACAAGCCTGT | 7874 |
rs575798959 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8933804 | TCTATCTCCCAGGCT[A/G]GAGTGCAGTGGTGTG | 7874 |
rs575800403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8946545 | CGTATCTTACAAAGA[C/T]TCAAATCTCAAATAT | 7874 |
rs575837960 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8951334 | CTGAGCCTCTGGTAG[A/C]CCTGACCCAGTTTTC | 7874 |
rs575843043 | in-del | -/AAAA | 0.412857 | 0.189678 | intron-variant | USP7 | GRCh38.p7 | 16:8901321 | ACAAACAAAAAAACG[-/AAAA]AAAAAAAACAGTAAG | 7874 |
rs575908745 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8939778 | AACTCCAAAACATTG[A/C/T]CATGATTTATCAACC | 7874 |
rs575930078 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8898151 | GGCTGCCGAATGGTT[C/T]CTTAGCTCCACATGT | 7874 |
rs575959733 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8914273 | TTCAAAGTCTGGCAA[C/G]TGACAGCTCCAGTGT | 7874 |
rs575970645 | snp | C/T | 9.88484e-05 | 0.00702954 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8897028 | TGCTTTCTCCCCAAG[C/T]TCCACGGCCTTTTTA | 7874 |
rs575974528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8930451 | CATGGCTTTAATAGA[A/G]TAAGCAAAATATAAA | 7874 |
rs576053843 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8916856 | GTCTATTTCCAAAGA[C/G]ATAAAACAAAATACA | 7874 |
rs576076407 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8948368 | TTGGCATTTTTTTGT[A/G]GAGACGAGTTTTCAC | 7874 |
rs576122299 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8944266 | CCAAAATACTGGCTG[A/T]GGCTTGACACCCCCT | 7874 |
rs576125801 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957445 | CTATTTGTTACTCAT[A/G]CAAAAAACCATAAAC | 7874 |
rs576127791 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892579 | AAACCTTTCATTTCT[C/T]AAGAGTAAATGTGAC | 7874 |
rs576136671 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8917303 | TTTTAACGATCCCCA[A/C]ATTGGTGAGAAAGTT | 7874 |
rs576153317 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8954513 | GATTACCCTGTTAAC[C/G]GTAACTCAAAAAGTC | 7874 |
rs576158874 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8948727 | AAAAGCAGCCAAAAA[C/G]AAGCATGGACAACAC | 7874 |
rs576188159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8943805 | CATTCCCCAAGAAAA[C/T]GAGCATTCACGCTGG | 7874 |
rs576188415 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8935463 | TGATCTGCGCACCTC[A/G]GCCTCCCAAAGTGCT | 7874 |
rs576226378 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964502 | CAAGAGCAACCCCAG[G/T]CGGGGCGCAGCTGCT | 7874 |
rs576241987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8959020 | TAGTTCTAACATAGT[A/G]TCACATTTTCTTGGC | 7874 |
rs576294303 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8908767 | ATTTGCTGCTGTGTT[-/A]ATACAGTCATTAAAC | 7874 |
rs576325515 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8947893 | GTGTGCAATTCGGAA[A/G]GTGGGAGTAAAGCAG | 7874 |
rs576338830 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8929891 | GATTCATAGCTATCA[C/T]CAACTGATATACACC | 7874 |
rs576359821 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP7 | GRCh38.p7 | 16:8954680 | GTTTGCGTAGTTTAA[C/T]AACAGCAATTGCAGG | 7874 |
rs576363477 | snp | G/T | 0.00597247 | 0.0543191 | utr-variant-5-prime, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8963442 | GGCGGCCCCGGGGCG[G/T]CCCGCGGCGGGCGGC | 7874 |
rs576396734 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8914067 | AATATTTCTTTAAAG[G/T]AATGACTATAAATCA | 7874 |
rs576484751 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8931102 | AAAACAATTCTACAG[C/G]CAATTTTGTTGTGAA | 7874 |
rs576498798 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964307 | GCCGGGGCGAGCGCT[A/G]GAGGTTGCCCGGGGA | 7874 |
rs576507935 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8929346 | AGGTAACAAAGCAGC[A/G]GGTTTAGACCACGCC | 7874 |
rs576522557 | snp | A/G | 6.69994e-05 | 0.00578751 | intron-variant | USP7 | GRCh38.p7 | 16:8903225 | GGAAGGAAGGTGGAC[A/G]TTGGGAGCCACGGTG | 7874 |
rs576526804 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8925631 | CTGCTGCCCAGCCCC[A/G]CAGAGGCCACCGCGC | 7874 |
rs576538417 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | USP7 | GRCh38.p7 | 16:8894434 | CTGGTTCCACAGGTC[C/G]GCCAGTGGAGAGAGA | 7874 |
rs576577170 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8927090 | GAGGCCGGGGTGGGC[G/T]AGGCGAATCATGAGG | 7874 |
rs576582772 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894215 | CCAAGGGGTAAGTTC[A/G]CAGGGAAGCCAGGAC | 7874 |
rs576592448 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950066 | TGGCTGTTGTGACAG[A/C]GGAATTGGTATTATT | 7874 |
rs576594925 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP7 | GRCh38.p7 | 16:8926686 | TATGCTAGGTATTAG[C/G]AAGGACACCCACATT | 7874 |
rs576639937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8903621 | ACGGTGGCTCATGCA[C/T]TTTGGGAGGCCGAGG | 7874 |
rs576642747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961641 | ACCTGGAAAGCGGTA[A/G]GACAATGTCATGGGA | 7874 |
rs576644574 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8956063 | ACACTTTCCAAACCA[C/G]ATGCCAGTTTAACAA | 7874 |
rs576645868 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8906077 | CAAGGTAGGACCAGG[C/G]GGCACGCAGAGGGAC | 7874 |
rs576657158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8949717 | GCCCTCATTATTTGC[C/T]CATATGACCTATCTG | 7874 |
rs576670393 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8917665 | ATTATAGGCGAGAGC[C/T]ACCGCACCCAGCCTC | 7874 |
rs576714503 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP7 | GRCh38.p7 | 16:8932719 | GTTTTATGAGATTCA[C/T]AAATTGTAAACCAAG | 7874 |
rs576734121 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937356 | TTGAGACCAGCCTGG[C/G]CATGGCAAAACCCCA | 7874 |
rs576757319 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956531 | ACACTTTGGGAGGCG[A/G]AGGCGGGCAGACTGC | 7874 |
rs576802606 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8944783 | GGGCTGTCAGATCTT[C/T]TGAAAAACTAGCGTC | 7874 |
rs576818348 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8922442 | GTGGTGAGCCAAGAT[A/C]AGGCCACTGCACTCC | 7874 |
rs576862036 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8900825 | TTCTACAACAGGTAA[A/G]AAAAAAAAATTCACA | 7874 |
rs576870357 | in-del | -/A | 0.342358 | 0.232314 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938339 | AGAAATAACACAGTC[-/A]AAAAAAAAAAAAAGA | 7874 |
rs576879972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8905963 | GGCCCTGTGGTCTTG[A/G]GGGTAGATTCCAAGA | 7874 |
rs576882874 | in-del | -/TATC | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8929015 | AGAAGCTCCGCCCTA[-/TATC]TATGTCTCCTCCCAA | 7874 |
rs576924488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8896075 | CGAACTCCTGACCTC[A/G]TGATCCGCCCGCCTC | 7874 |
rs576928826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8905037 | TCTGCATCGAAACGC[A/G]CAAGCCCAACCCTGC | 7874 |
rs576954289 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8929167 | GGCTAGAATTGATCC[C/T]AAACGCACACCTAGC | 7874 |
rs576967873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8911484 | ATCCAGAGTGTATGG[A/G]GAGCTCGTCCTGCTC | 7874 |
rs577030490 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8919987 | CTTCCCCCAGTCCCC[C/G]CTTCCTCACACTCGG | 7874 |
rs577064310 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP7 | GRCh38.p7 | 16:8919619 | TTTTTTATTTTGTGA[C/T]TTTGGTGGTTGTTTG | 7874 |
rs577088706 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8910532 | GACCCTCCGGACTGC[C/T]GGATGTGCTTCTACA | 7874 |
rs577102036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8924389 | TTCACTTTCTGTACC[C/T]ATCTCATTATAGTCT | 7874 |
rs577112415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8902751 | AAATCAGCTGGGCCT[A/G]GTGACGGGTGCCTGT | 7874 |
rs577136492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8928784 | TTTCGGGTCCTATGG[C/T]GTGGCACCACTGTCT | 7874 |
rs577171027 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8947095 | CATTCCTCCTGTTTT[C/T]TTCAGTATATCTCTG | 7874 |
rs577209952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8924907 | GAAGGAAGAGCAGCT[A/G]AAAGAGGCGCATCTT | 7874 |
rs577215061 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8946392 | TCAAGACCAGCCTGG[A/C]CAATATGGTGAAACC | 7874 |
rs577222685 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8911856 | AACCAGCAAGAGGAT[G/T]AGGATTGGGGGGAAC | 7874 |
rs577271254 | snp | A/T | 3.40304e-05 | 0.00412481 | intron-variant | USP7 | GRCh38.p7 | 16:8908458 | TCTGCTTCCTAAACA[A/T]TGAAAAACAAATGCA | 7874 |
rs577310840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8916368 | ACATCTGCTGCCTTT[C/T]TGTAGCCTAAGTCTG | 7874 |
rs577329828 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8934176 | TGGATGCAAAAATGA[C/G]GGCTCATTTTCTGTA | 7874 |
rs577356250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8913184 | AACATGGTGAAACCT[C/T]GTCTCTACTGAAAAT | 7874 |
rs577381312 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8903188 | CCTACCCCCAAAGGC[A/G]ATCAGTATTTTCTAG | 7874 |
rs577388517 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938157 | CTGAGCAAACAGGCA[C/G]GACACTCCGAGAAGG | 7874 |
rs577388621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8943341 | TGTACTGCTTCTACA[C/T]GTATAGTCTGCTCCG | 7874 |
rs577413114 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8947480 | CAGCCTCCTGATTAG[C/G]TGGACTACAGACATG | 7874 |
rs577418846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962578 | GCTGCACCACACACT[A/G]CCAAGTACAAACTCC | 7874 |
rs577427642 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8909164 | TCTATCACTGCTCCA[C/T]CTTGGCCAGCTCTTT | 7874 |
rs577449881 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8896731 | ATACAAGGGGAAGGA[A/G]GAAAAACGTGGCTTA | 7874 |
rs577488966 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8930025 | GCAGTGGCTGGAGAC[C/G]TGCAGGCAGGAGTAA | 7874 |
rs577494754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8902244 | CTTAGGTGACAGAGC[A/G]AAAAACTACAGTCAA | 7874 |
rs577531132 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956505 | CGCAGTGGCCCACGC[A/C]TGTAATCCCAACACT | 7874 |
rs577541185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8949667 | TTCAATTTCCAGGCC[C/T]CTATCTGCTCACCTC | 7874 |
rs577560490 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8922334 | CCCTATGAAAAATAC[-/A]AAAATTAGCTGGGTG | 7874 |
rs577640980 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8927270 | GAGGGTGAGGTGAAC[C/T]GAGATTGCGCCACTG | 7874 |
rs577652810 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8914851 | CTGAGTCCTGGAGTT[C/T]GAGGCTGCACTGAGC | 7874 |
rs577683824 | snp | A/C | 0 | 0 | intron-variant | USP7 | GRCh38.p7 | 16:8923671 | TCAGACTGAGTTCCA[A/C]ATGAGAACAATGTCT | 7874 |
rs577686928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8944874 | ACTTGGGAGGCTGAA[A/G]TGAGGGGCAGATCGA | 7874 |
rs577706505 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8917942 | CTACAGGTGCACGCC[A/G]CCATGCCCAGATAAT | 7874 |
rs577711706 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937973 | CATGAATCAGTAACT[C/T]CAATGAGCCCCTATT | 7874 |
rs577716032 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8935892 | CTGCTACCCCACCAG[A/T]GAACACCTCCCAATC | 7874 |
rs577716891 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8922980 | CAGCTAATCCAGGCC[A/G]GCCCTGATTCCATGG | 7874 |
rs577788782 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP7 | GRCh38.p7 | 16:8946125 | GCCCCTCCCCCACAA[A/G]ACTCTCAACCTAAAC | 7874 |
rs577791881 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893013 | AACTACACACAATGA[A/G]TATCAACATCAGTGA | 7874 |
rs577798624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8940205 | TCCTGCTGCCTATCT[A/G]CGCATCCTATAGCCA | 7874 |
rs577802237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8939838 | AGCGCAGTGGCTCAC[A/G]CCTGTAATCACAGCA | 7874 |
rs577837434 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8917222 | TTTAAAAAACAGTAA[A/G]AATTTAATCTTCATG | 7874 |
rs577845887 | snp | A/C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8931392 | GTGGTTTCACCATGT[A/C/T]GGTCAACTGGTCTCG | 7874 |
rs577857042 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8904681 | GGCGTGGTGGCTTAC[A/G]CCTGTAATCCCAGCA | 7874 |
rs577883808 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8936245 | TTATTACGGCAGATA[C/G/T]GCATGGGCCAACACC | 7874 |
rs577884963 | snp | C/T | 0.000133721 | 0.00817574 | intron-variant | USP7 | GRCh38.p7 | 16:8904408 | GGCTGCATGGTGACC[C/T]GGAGTCCCAGAAGGG | 7874 |
rs577903940 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8941675 | AGACAAAGACCAGGC[A/C]GTGTTGGTGTGGTGA | 7874 |
rs577930830 | in-del | -/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961997 | CAACCTGGCCAGCCA[-/T]TTTTTTCAGTGACTA | 7874 |
rs577959497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8940627 | CAGGGACGATGGTGG[C/T]AGCCAAAAAAGACGG | 7874 |
rs577989464 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8899831 | AAAAATGGCATCATC[A/T]TTTACACAACAGTGA | 7874 |
rs577991059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8932079 | CCCTCCAAGAACTCT[C/T]CAAAACCCCAACGCT | 7874 |
rs578010135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8918566 | TATAATCTGAGCCCC[C/T]TGGGAAGCTGAGGCA | 7874 |
rs578026726 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950460 | CTGATCATTAAGAGT[A/C]AATGCAGATGTGTGG | 7874 |
rs578030576 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8965167 | CTCCCATTTATGTAC[C/T]GTTCATCTCCCTTCC | 7874 |
rs578043162 | snp | A/T | 1.6476e-05 | 0.00287014 | intron-variant | USP7 | GRCh38.p7 | 16:8894738 | TACGCTAGGCAAGGC[A/T]TGAGCCTATGGCCCG | 7874 |
rs578047366 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8955513 | AGCTCATGAGGTCAG[C/G]CCTGGCCAACATGGG | 7874 |
rs578088087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | USP7 | GRCh38.p7 | 16:8894506 | GACCACTTGTTTCTT[A/G]GTCTGAAACCCACAC | 7874 |
rs578095081 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8909949 | AAGCAACTTTCTGAT[C/G]TATACCTCAGTCCCT | 7874 |
rs578095927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8913984 | TTCAAGCAATCCTCC[C/T]GACTCAGCCTCCCAA | 7874 |
rs578109065 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP7 | GRCh38.p7 | 16:8918887 | CCAGCACTGGGGAAT[G/T]AAAACGCAGCATGAA | 7874 |
rs578195916 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant | USP7 | GRCh38.p7 | 16:8896797 | GCTTGAGGGTTACCC[-/CT]GAGACTTGAAAAACT | 7874 |
rs578237920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP7 | GRCh38.p7 | 16:8910255 | GCTGGCCACCTGGTC[A/G]CCCACCATGCTCACT | 7874 |
rs745313308 | snp | A/C | 4.97772e-05 | 0.0049886 | intron-variant | USP7 | GRCh38.p7 | 16:8894687 | ATTTCTGTATATCAG[A/C]AAAACTCACATCTCT | 7874 |
rs745314105 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8939915 | CCATCCTGGCTAACA[A/C]GGTGAAACCCCGACT | 7874 |
rs745320804 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8930154 | AACCCAAACAGGATT[G/T]TCCTCAGTTACAGCC | 7874 |
rs745354893 | snp | A/G | 1.77087e-05 | 0.00297557 | intron-variant | USP7 | GRCh38.p7 | 16:8923427 | GTCTGCAAAAAAAAC[A/G]CATCATCAGTCACAG | 7874 |
rs745417051 | snp | C/G | | | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962517 | CAGGCAGCCATGTGC[C/G]GCAGGGCTTTCGCAC | 7874 |
rs745423187 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8939390 | TTCTCCTGTACTCTA[A/G]GATATCATGGCAGGG | 7874 |
rs745466906 | in-del | -/GA | | | intron-variant | USP7 | GRCh38.p7 | 16:8946436 | AAGAAAAAAACTGTT[-/GA]TCAACTTTGCTCCAG | 7874 |
rs745496675 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8948644 | CACACGATGGAATAT[C/T]ATTCTGCGAGAAAAG | 7874 |
rs745498431 | snp | C/T | 1.65594e-05 | 0.0028774 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8894628 | GGCCCATCATTACAA[C/T]TGCAAATTTAAACTA | 7874 |
rs745523000 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8947766 | AGGATCCTGCCATCA[A/G]AAACTTAGCTATTCC | 7874 |
rs745579723 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8908596 | GTCCATTTAGGGCAT[A/C]TTTGAAATGTTTTCT | 7874 |
rs745616058 | snp | G/T | 3.29777e-05 | 0.00406051 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893948 | AAAGTTCTAGGCTGT[G/T]AAGGGGCCACCCACA | 7874 |
rs745619920 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8935028 | GACTTCTAGAAATAG[C/G]CTAAACGATAAGGCT | 7874 |
rs745631851 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8905675 | TTACAGAATTAAAAA[A/G]GCCATACTGAGCACA | 7874 |
rs745639108 | snp | C/T | 6.59533e-05 | 0.00574215 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8917138 | AATCATCCCCCTCGG[C/T]TGGCATCATGTACAC | 7874 |
rs745660033 | snp | A/C | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8905227 | TAACATGTAAGCATT[A/C]GTGCAGTGTCGAACA | 7874 |
rs745694795 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8911135 | GAAGACAGCTTGGAA[C/T]TGGGCAGTGTGGACA | 7874 |
rs745759042 | snp | A/C | 1.67315e-05 | 0.00289231 | intron-variant | USP7 | GRCh38.p7 | 16:8930257 | TTTTCTGACAAGTTT[A/C]CGCCCACTGCGAGGC | 7874 |
rs745779620 | snp | A/T | 1.65042e-05 | 0.0028726 | intron-variant | USP7 | GRCh38.p7 | 16:8895614 | CTCATGAATTCTCTC[A/T]GGTGCCAACAGTATC | 7874 |
rs745792287 | in-del | -/TCCTCCATG | 1.65304e-05 | 0.00287488 | cds-indel, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8930295 | CACAGGCACTTACCA[-/TCCTCCATG]TCCTCCTCCGCGGTG | 7874 |
rs745792773 | snp | C/T | 3.29685e-05 | 0.00405995 | intron-variant | USP7 | GRCh38.p7 | 16:8899808 | GTCCATGGCAGGGGG[C/T]AGCTGGTAAAAATGG | 7874 |
rs745801562 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8920978 | TGAGACGTGAATCCA[G/T]AAAGCTGCTAAAAAC | 7874 |
rs745820933 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8896502 | AGTAGTGAGAATCAT[A/G]CCCATCTCTCTGAAA | 7874 |
rs745855649 | snp | C/G | 3.29484e-05 | 0.00405871 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8899702 | CGCGGTGGTAGAGAT[C/G]TCGGAAATACTCCTT | 7874 |
rs745866621 | snp | A/G | | | intron-variant, missense | USP7 | GRCh38.p7 | 16:8894472 | GCACTTGACCCTGGG[A/G]CTGCCCCTCCCAGCC | 7874 |
rs745870659 | in-del | -/ACACAACG/GTACAACG | 0.101108 | 0.205668 | intron-variant | USP7 | GRCh38.p7 | 16:8923202 | GCTTCCAGTAATGAA[-/ACACAACG/GTACAACG]ATACTGTCTTACGTG | 7874 |
rs745879408 | snp | A/G | 6.58946e-05 | 0.0057396 | intron-variant | USP7 | GRCh38.p7 | 16:8895004 | CAGGTTTTGACGTGA[A/G]CCACTCGGCCAACCA | 7874 |
rs745882587 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8940461 | TCCAAGAAGCTGGGC[A/G]CCACCATCAAGGCTG | 7874 |
rs745937604 | snp | A/G | 1.64846e-05 | 0.0028709 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8915315 | TCTTCTATCAGACCG[A/G]TAGTCTACTTCTTTA | 7874 |
rs745946165 | snp | A/C | 1.64838e-05 | 0.00287083 | intron-variant | USP7 | GRCh38.p7 | 16:8915421 | ACCTTTAAAAATCAT[A/C]TTTTAGAACTGGTAG | 7874 |
rs745960682 | snp | A/G | 1.65433e-05 | 0.002876 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8899162 | CATTGGATCTGTGTT[A/G]AGCCTCTGTGCAACT | 7874 |
rs745995712 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950350 | CTGATAAACACTCAA[A/G]ATTAAAACAGTATTT | 7874 |
rs746015617 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8928699 | AAGGAAAGGTGCTAC[A/G]GAAGATTACTCAACC | 7874 |
rs746017831 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8919489 | ACTTATCACACGCAA[A/G]GTCAGCACAACGTGG | 7874 |
rs746030691 | snp | C/T | 1.70664e-05 | 0.00292112 | intron-variant | USP7 | GRCh38.p7 | 16:8921312 | TGTTTAAAAGAATAA[C/T]CTGAGCCTTAGTTGA | 7874 |
rs746083739 | snp | A/C | | | intron-variant, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8949603 | TTAAGGCCCACCACA[A/C]CACCACCTCTTCACC | 7874 |
rs746104999 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8928031 | TCATCTCATGAAAAA[C/T]AGTGAATAAGGAACT | 7874 |
rs746116587 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8904247 | CTCTCTGGGCAGCTG[C/T]CCTGCTGTGCAGTGA | 7874 |
rs746119095 | snp | C/T | 3.60399e-05 | 0.00424484 | intron-variant | USP7 | GRCh38.p7 | 16:8902334 | AGTGCAGAGGACTAA[C/T]GCCTTCTGCACGGTT | 7874 |
rs746153904 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8946958 | CTGGAAAAAATCCAC[G/T]GAAAGTGCATGACGA | 7874 |
rs746155820 | snp | G/T | 1.65051e-05 | 0.00287267 | intron-variant | USP7 | GRCh38.p7 | 16:8899070 | GATGTTTCAATGAAC[G/T]GTGGAAAGCATGCAG | 7874 |
rs746161415 | snp | C/T | 4.94662e-05 | 0.00497299 | intron-variant | USP7 | GRCh38.p7 | 16:8901095 | AATGTGTAGCTGTAA[C/T]GTACTGAGCAAAATC | 7874 |
rs746172374 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8924804 | CATGTGTGACGGTAA[A/G]CACTTCTACCTTCTT | 7874 |
rs746189006 | in-del | -/AAA | 2.8939e-05 | 0.00380377 | intron-variant | USP7 | GRCh38.p7 | 16:8902530 | AACACGCTCATATTT[-/AAA]TAGTCCTCTATATTA | 7874 |
rs746239493 | snp | A/G | 1.65564e-05 | 0.00287714 | intron-variant | USP7 | GRCh38.p7 | 16:8904581 | CTGCAGGACAAAGGC[A/G]TCCTCTTTGACCCCT | 7874 |
rs746243990 | in-del | -/CCA | 4.95119e-05 | 0.00497529 | intron-variant | USP7 | GRCh38.p7 | 16:8899104 | AGACCAAGCAAGTGT[-/CCA]CACATGTGACCTACC | 7874 |
rs746253388 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956632 | AGCCGGGCATGGTAG[C/T]GTGTGCCTGTAGTCC | 7874 |
rs746318091 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8900869 | CATTCTCAAGATCAT[C/G]TGAGGCCCTGAGTTA | 7874 |
rs746399740 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8932940 | ATAAATTATGGCACA[G/T]TCCAATGGAATTTTT | 7874 |
rs746412580 | snp | A/C/G | 0.00013179 | 0.0081166 | missense, synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8904489 | CCGCTTCTGAGCCTC[A/C/G]ATCCTTTTCTCTTCT | 7874 |
rs746434929 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8918903 | AAAACGCAGCATGAA[A/C]TAGCAGCCATCTGAG | 7874 |
rs746438324 | snp | C/T | 3.29614e-05 | 0.00405951 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8895147 | CCTGGTCCAAAGGGA[C/T]TTCCTGGGGACACGG | 7874 |
rs746454653 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8954834 | GTGCGGTGAGGGGCG[A/C]CTGTAGTCCCAGCTA | 7874 |
rs746462829 | snp | A/G | 3.39737e-05 | 0.00412137 | intron-variant | USP7 | GRCh38.p7 | 16:8900491 | TAAAAAAATCCTGAA[A/G]TTAGTACAAAGTGAT | 7874 |
rs746470804 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8930409 | CCCGCTTTAAAGAAG[-/A]AAAAGAAATTCCACG | 7874 |
rs746483502 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8921890 | AGCCAAAGAAAGTTA[A/C]GGTTTGCGATTTAAG | 7874 |
rs746508567 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8897995 | GCTTGGGGAGTAAGC[A/G]CAGAGTCATGGACTG | 7874 |
rs746519002 | snp | A/T | 5.20576e-05 | 0.00510158 | intron-variant | USP7 | GRCh38.p7 | 16:8916999 | AAAGAGGAAGCAGAA[A/T]GGCAAAGGCAGATGT | 7874 |
rs746553213 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8953440 | CTGCCACTAAGTAAA[C/G]TCTGAGGTACGATCC | 7874 |
rs746596833 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8896634 | CAGTTTCAGTTCATC[A/G]TTCAAATGGAATCGT | 7874 |
rs746614660 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8907885 | CAAACAACTACTTTA[C/G]CATTCTTGAAAACTC | 7874 |
rs746650858 | in-del | -/AGA | 1.67687e-05 | 0.00289552 | intron-variant | USP7 | GRCh38.p7 | 16:8903425 | TATGTATGAAAGCAC[-/AGA]AAAGACTTGACAACT | 7874 |
rs746672928 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8906952 | TTTAATATTCTACAG[A/G]CATCCTGAAATTGAC | 7874 |
rs746704153 | in-del | -/CA | 1.66018e-05 | 0.00288108 | intron-variant | USP7 | GRCh38.p7 | 16:8899211 | ACAGAAAGGAAGGTT[-/CA]CATTTTGGGGAAAAA | 7874 |
rs746706683 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8918133 | ACTTGTGAAACAAAG[A/G]TTTGATTAAAAACTT | 7874 |
rs746724940 | snp | C/G | 3.31235e-05 | 0.00406948 | intron-variant | USP7 | GRCh38.p7 | 16:8910839 | AATACTTTAAAGAGA[C/G]AGAGAGAAAAGTCAA | 7874 |
rs746759407 | snp | A/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8902131 | AGCAGCCAGCTCGGG[A/T]TCAACTGTTTCCAGG | 7874 |
rs746763855 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8959620 | GCAACAGAAGCCAAT[A/G]TAAGGAAAATCAACA | 7874 |
rs746767585 | snp | A/G | 3.29592e-05 | 0.00405938 | intron-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894132 | AAGAAAAGCAAGTGA[A/G]GCCACAGAGCAGCCC | 7874 |
rs746768110 | snp | C/T | | | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962606 | TCCCCGAAAAACAGG[C/T]GGATTCGGAAACCAA | 7874 |
rs746777348 | snp | C/T | 3.30453e-05 | 0.00406467 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8903385 | TTGGTGGCCACAAAA[C/T]TGGTCCTCTGCGACT | 7874 |
rs746779922 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937098 | AGGAGGAATAATTGA[C/T]GTAAGTGAAAAATTT | 7874 |
rs746821104 | in-del | -/C | 1.80549e-05 | 0.00300452 | intron-variant | USP7 | GRCh38.p7 | 16:8930419 | GAAGAAAAAGAAATT[-/C]CCACGGGTTTTACAT | 7874 |
rs746837727 | snp | C/T | 1.64789e-05 | 0.0028704 | intron-variant | USP7 | GRCh38.p7 | 16:8905353 | GGAAAACAACACACA[C/T]CAGCAGCGATCAAGC | 7874 |
rs746859244 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8913705 | GAGCATTGCAAGCTG[A/T]AAATATGTGGGTCAA | 7874 |
rs746869990 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8945820 | CTTTAGGAAGCCAAG[A/G]CAAGAAGACTGCTTG | 7874 |
rs746887257 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894028 | AATGGCCTTTTCAAG[A/G]TAAGTGTAGCGACTC | 7874 |
rs746902333 | in-del | -/CA | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950853 | TCACTTGTTTCTGCG[-/CA]CACAGTCACTCCTGA | 7874 |
rs746915946 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8945243 | AAAAAAAATAGCCAG[A/G]TGTGGTGGTGCACAC | 7874 |
rs746928422 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8922392 | ACTTGAGACGCCGAG[A/G]CAGGAGAATCGCTTG | 7874 |
rs746945723 | snp | C/G | 1.65192e-05 | 0.00287391 | intron-variant | USP7 | GRCh38.p7 | 16:8896960 | CGTTAACTGCCACCC[C/G]TAACTGAACGTCCAC | 7874 |
rs746988137 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8945459 | TTGTTTTATTTGTTC[-/A]TGGGTTAGTGGGGGC | 7874 |
rs746989311 | snp | A/G | 7.08253e-05 | 0.00595043 | intron-variant | USP7 | GRCh38.p7 | 16:8895744 | AATTTCTAGCAGCCT[A/G]AACAGAGAGGAAAAA | 7874 |
rs747014527 | snp | C/G | 1.6495e-05 | 0.0028718 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8900584 | AGGGCTTTATCAAGA[C/G]ACACGTCATAGTCCT | 7874 |
rs747036799 | snp | C/T | 5.14655e-05 | 0.00507248 | intron-variant | USP7 | GRCh38.p7 | 16:8900957 | ACAAACTACTAAGAA[C/T]ATACTAATTATGGAA | 7874 |
rs747047232 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8934182 | CAAAAATGAGGGCTC[A/G]TTTTCTGTACATAAA | 7874 |
rs747062078 | snp | C/T | 6.42199e-05 | 0.0056662 | utr-variant-5-prime, intron-variant | USP7 | GRCh38.p7 | 16:8936619 | TCCCAGCCATCTCTG[C/T]ATGGCTCTGCAGTGG | 7874 |
rs747065348 | snp | C/T | 1.64746e-05 | 0.00287002 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8904516 | TTCTTGTAATCGCTC[C/T]ACCAACTGCTGAGGA | 7874 |
rs747070958 | snp | A/G | 1.65318e-05 | 0.002875 | intron-variant | USP7 | GRCh38.p7 | 16:8895592 | TTTAAATATGCAGCA[A/G]ATGGGGCTCATGAAT | 7874 |
rs747092052 | snp | A/C | 3.3036e-05 | 0.0040641 | intron-variant | USP7 | GRCh38.p7 | 16:8916457 | TTCTGACCATGCTTC[A/C]AAATATTCATTGTAA | 7874 |
rs747105981 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8942714 | CACCACACTCAGCTA[A/G]TTTCTGTATTTTTTT | 7874 |
rs747150020 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8910664 | TGAAAAGGCACAAGC[A/T]AATTTTTATTTAGCA | 7874 |
rs747177803 | snp | C/G | 1.64825e-05 | 0.00287071 | intron-variant | USP7 | GRCh38.p7 | 16:8895156 | AAGGGATTTCCTGGG[C/G]ACACGGACAACAGAC | 7874 |
rs747177984 | snp | A/C | 1.67522e-05 | 0.0028941 | missense, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8923401 | AAGGTTGCCTCGGAG[A/C]GCCAACTGGTGTCTG | 7874 |
rs747180128 | snp | C/T | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8915452 | CCACATACCACCATT[C/T]TGCCGCGGAATAATT | 7874 |
rs747191768 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8951840 | ACCTGATTCACAAAG[C/G]AAGCAATCTACCAAC | 7874 |
rs747214944 | in-del | -/TT | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957377 | ATGTTGTTACAACTC[-/TT]GTTCTCCAGGATAAA | 7874 |
rs747248809 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8941841 | CTGGGCCCAGGGTTC[A/G]GCAGGGAACTGGGTG | 7874 |
rs747261595 | snp | C/G | 4.97137e-05 | 0.00498542 | intron-variant | USP7 | GRCh38.p7 | 16:8899574 | TTTCTGGAGTGGGAT[C/G]TGAAGAGGAAAGGAG | 7874 |
rs747295641 | snp | A/G | 0.000115316 | 0.00759243 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893994 | GAACACACCAGCTTG[A/G]AAATCAGTTATGGAT | 7874 |
rs747307611 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8939455 | CTGGGTCCTTTCCAG[A/G]TAGAGGAAATTCACA | 7874 |
rs747309292 | snp | A/G | 1.65222e-05 | 0.00287417 | intron-variant | USP7 | GRCh38.p7 | 16:8898500 | GAGCCTTCTCTTTAT[A/G]ACCCATAGTTACATT | 7874 |
rs747314351 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8917281 | TGGCTAAGGTTGTTG[C/T]TAGGGCTTTTAACGA | 7874 |
rs747317545 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8919003 | AGGGTGAGCGGAAGG[C/T]TGCAGGAGAGGAACA | 7874 |
rs747320881 | snp | A/G | 5.3638e-05 | 0.00517843 | intron-variant | USP7 | GRCh38.p7 | 16:8908501 | CTCTACTTACTCCTG[A/G]AAGCAATGAAAGCAA | 7874 |
rs747330865 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8892224 | AAGACAAACCCACAG[C/T]GAACGGCTCTCGCAC | 7874 |
rs747350145 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950182 | TATTTATGTATTTAA[C/T]TTAATCAACCACATG | 7874 |
rs747357236 | snp | C/G | 1.64792e-05 | 0.00287042 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8901200 | CAAGCTCCGCGTTTT[C/G]GGATCATACATCTTC | 7874 |
rs747378750 | in-del | -/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8915175 | GACTATTTAAAAAAA[-/C]ATCACTTGTGTAAAT | 7874 |
rs747395726 | snp | A/C | 1.84018e-05 | 0.00303324 | intron-variant | USP7 | GRCh38.p7 | 16:8920497 | AAGAACACACATTTT[A/C]TTCCCAAGAGACAAA | 7874 |
rs747399453 | snp | A/G | 1.65332e-05 | 0.00287512 | intron-variant | USP7 | GRCh38.p7 | 16:8898440 | TTTTCATCTTAAGCT[A/G]TTAAGAAAAGAAAGA | 7874 |
rs747448114 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8925457 | TTTTATATAATTCAG[C/T]TCTTTACAGGGTTTG | 7874 |
rs747458090 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8902216 | AGACGCTGATTTTAG[A/T]AGAGTCTAATGGCTT | 7874 |
rs747467447 | snp | A/C | 1.9845e-05 | 0.00314994 | utr-variant-5-prime, intron-variant | USP7 | GRCh38.p7 | 16:8936710 | TAGGAGCTCTACCTC[A/C]GCATTCTTTTTTATT | 7874 |
rs747474872 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8916118 | GCTCAATGAGAACCT[C/T]GCTGCACAGGAGGGG | 7874 |
rs747517951 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957477 | GGCTGGGTGAGGTGG[C/G]TCACACCTATAATCC | 7874 |
rs747533929 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8934733 | AGGTGCAGAGAAAGT[C/G]GTCAAGGCCAGTGGC | 7874 |
rs747535891 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8924889 | TACAGCACAGGAACT[G/T]TGGAAGGAAGAGCAG | 7874 |
rs747583280 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8901865 | GAAGACAGAACAGGA[C/T]GGCCCCACGTGGCTG | 7874 |
rs747591167 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8945992 | TGGCAAAGGAACGGA[C/G]AGGGGAGAATGGAAG | 7874 |
rs747595064 | snp | G/T | 1.65138e-05 | 0.00287343 | intron-variant | USP7 | GRCh38.p7 | 16:8896966 | CTGCCACCCCTAACT[G/T]AACGTCCACAATTGG | 7874 |
rs747595600 | snp | A/G | 9.89234e-05 | 0.0070322 | intron-variant | USP7 | GRCh38.p7 | 16:8901102 | AGCTGTAATGTACTG[A/G]GCAAAATCTACTCAG | 7874 |
rs747604903 | snp | A/C | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8919046 | CTTTCGTAGCTGATT[A/C]GTGAAAAATAACGTC | 7874 |
rs747616810 | in-del | -/A | 3.39951e-05 | 0.00412267 | intron-variant | USP7 | GRCh38.p7 | 16:8903445 | GACTTGACAACTGAC[-/A]AAAAAATGAGTCCAC | 7874 |
rs747642811 | in-del | -/AA | 3.32027e-05 | 0.00407434 | intron-variant | USP7 | GRCh38.p7 | 16:8910846 | TAAAGAGAGAGAGAG[-/AA]AAGTCAAGTGCTAAA | 7874 |
rs747673292 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8913788 | GAGATACTTGCTCTG[G/T]TGCCCAGGCTGCAGT | 7874 |
rs747678622 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8955556 | ACTAAAATACAAAAA[A/C]TTAGCCGGGCATGGC | 7874 |
rs747684595 | snp | C/T | 1.65496e-05 | 0.00287655 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8900619 | TCTCTCTGTTAAATT[C/T]GGTTTAACTTCCTAC | 7874 |
rs747705679 | snp | C/T | 1.66632e-05 | 0.0028864 | intron-variant | USP7 | GRCh38.p7 | 16:8917184 | AGAAATAAGAATTTT[C/T]ACTCTGAGAAGATGC | 7874 |
rs747762833 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8922545 | ACTCTGGGGAACATG[G/T]TACTGAGGGTTCCAA | 7874 |
rs747781046 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8899028 | TGTCAGGTGAAATGG[C/T]GAGCTAATTATTAAA | 7874 |
rs747795179 | snp | C/G | 1.65108e-05 | 0.00287317 | missense, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8930360 | CCCATTGATCACAGG[C/G]TTCTGAGTAATTCTT | 7874 |
rs747826123 | snp | C/T | | | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962801 | GGTGCGGGCGAGCCC[C/T]GCGCCCGGGGAGGTC | 7874 |
rs747843773 | snp | A/G | 1.6896e-05 | 0.0029065 | intron-variant | USP7 | GRCh38.p7 | 16:8900499 | TCCTGAAATTAGTAC[A/G]AAGTGATACAATCCT | 7874 |
rs747875713 | snp | C/T | | | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962278 | CGTAGGTAAGAAAAC[C/T]TTTTAAAGACCATTT | 7874 |
rs747922264 | snp | A/T | 3.3106e-05 | 0.0040684 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8899174 | GTTGAGCCTCTGTGC[A/T]ACTGTCTTTGCAACC | 7874 |
rs747946767 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892459 | GCAAGGCCGATGGGA[C/T]GGTGCAAGGACCACG | 7874 |
rs747965861 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961067 | TTACAGATTAACTGT[A/C]CTAGGGGTTACCTTT | 7874 |
rs747970385 | snp | A/G | 2.36337e-05 | 0.00343748 | intron-variant | USP7 | GRCh38.p7 | 16:8906624 | TCAGTATTAATTTAC[A/G]CAAAAAATATCACAC | 7874 |
rs748018881 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938265 | CACTATACTATACTG[A/C]CTTGATTAAACTTTT | 7874 |
rs748047715 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8925925 | TTTGGGAGGCAGAGG[C/T]GGGTGGATCACGAGG | 7874 |
rs748064888 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8914648 | ACACAGGCTGGACAT[A/G]GCAGCTCATGTCTAA | 7874 |
rs748099582 | snp | C/G | 3.60497e-05 | 0.00424541 | intron-variant, missense | USP7 | GRCh38.p7 | 16:8894499 | AGCCCCAGACCACTT[C/G]TTTCTTAGTCTGAAA | 7874 |
rs748128385 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8903544 | CCAATGAAGAAAAAC[C/T]GCATAAAATGACCAA | 7874 |
rs748187837 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8925630 | CCTGCTGCCCAGCCC[C/T]GCAGAGGCCACCGCG | 7874 |
rs748193010 | snp | C/T | 3.39726e-05 | 0.0041213 | intron-variant | USP7 | GRCh38.p7 | 16:8920451 | ATCGGTCACTTCCTA[C/T]AAAACATAAATAAGA | 7874 |
rs748209612 | snp | A/C | 0.000131846 | 0.00811822 | intron-variant | USP7 | GRCh38.p7 | 16:8901118 | GCAAAATCTACTCAG[A/C]AGGTAAGTGCACGAA | 7874 |
rs748213561 | snp | C/T | | | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891728 | GCTTTGCTCACAGCA[C/T]GAGCCACCGCGCCTG | 7874 |
rs748213775 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8934803 | ATAAGGGGTGGGTCC[C/T]GGCCACCAACAGCCC | 7874 |
rs748238953 | in-del | -/TT | | | intron-variant | USP7 | GRCh38.p7 | 16:8927170 | ACTAAAAATACAAAA[-/TT]AATTAGCCAGGCGTG | 7874 |
rs748239932 | in-del | -/C/T | 0.000250264 | 0.0111837 | intron-variant, frameshift-variant | USP7 | GRCh38.p7 | 16:8894536 | CAGCCCCCGGGGGGG[-/C/T]GGAGAACCCTTACCG | 7874 |
rs748273634 | snp | C/T | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8905201 | CTCAGTTTTGATTCC[C/T]TGATGTAGACTAACA | 7874 |
rs748305290 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8901909 | GCCTCACAGGAAACT[A/C]GCAGCCAAGTCAGTC | 7874 |
rs748360632 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8943729 | TTCCCAAAGGCAATA[C/T]GTATTAAAATCAAAA | 7874 |
rs748391686 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8922498 | TAAATTTTATTCCCT[A/G]GGGGATCTGACAGAA | 7874 |
rs748425961 | snp | A/G | 1.65124e-05 | 0.00287331 | intron-variant | USP7 | GRCh38.p7 | 16:8895602 | CAGCAGATGGGGCTC[A/G]TGAATTCTCTCTGGT | 7874 |
rs748433398 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8911448 | TGAGTGACAAGCTCT[A/C]AATCCAACACGGAAT | 7874 |
rs748456091 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8900908 | ACCTAACACTGTAAC[A/G]AATTCGGGGTAAAAA | 7874 |
rs748458211 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8920785 | AAGTAACATTCCTAA[G/T]ATTGTTCCACTGGTT | 7874 |
rs748469200 | snp | C/T | 1.6638e-05 | 0.00288422 | intron-variant | USP7 | GRCh38.p7 | 16:8910852 | GAGAGAGAGAAAAGT[C/T]AAGTGCTAAAGCTTC | 7874 |
rs748490594 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8908055 | CAAGAGCTGTGAAGC[A/C]GAAACAGCCCCATCC | 7874 |
rs748494190 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8900021 | CCCCTTAGGTAACAG[A/C]ACCTGCTCTCCTCTA | 7874 |
rs748520100 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8959357 | CCAAAACACTAATTC[-/A]AAAAAAAAAAAAAGG | 7874 |
rs748535939 | snp | A/C | 1.67503e-05 | 0.00289393 | intron-variant | USP7 | GRCh38.p7 | 16:8915231 | ATCAAAAGATCATGC[A/C]ATTAGATACACACAA | 7874 |
rs748564819 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8940027 | TGCTTGAACCAGGGA[A/G]GCGAAGGTTGTAGTG | 7874 |
rs748601932 | snp | C/G | 3.31631e-05 | 0.00407191 | intron-variant | USP7 | GRCh38.p7 | 16:8921114 | TAAGGGAACAACAAG[C/G]AGTAATGCACCAATT | 7874 |
rs748622408 | snp | C/G | 1.64762e-05 | 0.00287016 | intron-variant | USP7 | GRCh38.p7 | 16:8894740 | CGCTAGGCAAGGCTT[C/G]AGCCTATGGCCCGCC | 7874 |
rs748689294 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8926491 | TGGTCTCCAAAAAAA[C/T]TCAAGATAGGAGGGC | 7874 |
rs748704352 | snp | A/G/T | 3.33735e-05 | 0.00408483 | intron-variant | USP7 | GRCh38.p7 | 16:8898352 | TTCATAGTATTAAAA[A/G/T]AACTTACCTCTTCCC | 7874 |
rs748729390 | snp | A/C/T | 8.23915e-05 | 0.00641796 | intron-variant | USP7 | GRCh38.p7 | 16:8902071 | CAGGCAGGCGTCTCG[A/C/T]GGGCACTTACGATCT | 7874 |
rs748731017 | snp | A/G | 1.66838e-05 | 0.00288818 | intron-variant | USP7 | GRCh38.p7 | 16:8908297 | CTAACCCCCTAGACC[A/G]GCATGATGATGAAAT | 7874 |
rs748754803 | in-del | -/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8953002 | CACCATGCCAGGCTA[-/T]TTTTTTGTATTTTTA | 7874 |
rs748756838 | snp | C/T | 1.65244e-05 | 0.00287436 | intron-variant | USP7 | GRCh38.p7 | 16:8898512 | TATGACCCATAGTTA[C/T]ATTAATTTGGACTCA | 7874 |
rs748763196 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8916004 | GCCATTTCATGTTGT[A/G]TGTGTGTGCTTCTGC | 7874 |
rs748797684 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8904926 | GCAGTGAGCCGAGAT[A/C]GCGCCACTGCACTCC | 7874 |
rs748802227 | in-del | -/CT | 3.33356e-05 | 0.00408248 | intron-variant | USP7 | GRCh38.p7 | 16:8917186 | AAATAAGAATTTTTA[-/CT]CTGAGAAGATGCAGG | 7874 |
rs748815463 | snp | C/T | 1.65181e-05 | 0.00287381 | intron-variant | USP7 | GRCh38.p7 | 16:8919184 | CTTGCAGATACCCCA[C/T]TGCTCCTGCAGTGTG | 7874 |
rs748840212 | snp | A/G | 1.65143e-05 | 0.00287348 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8906508 | AGGACTGCATGAAGA[A/G]TATAATTTGCAGGGT | 7874 |
rs748841887 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892591 | TCTTAAGAGTAAATG[C/T]GACTAGTTAGAGGCT | 7874 |
rs748848436 | in-del | -/T | 0.000356279 | 0.0133421 | intron-variant | USP7 | GRCh38.p7 | 16:8906632 | AATTTACACAAAAAA[-/T]ATCACACTTTACAGT | 7874 |
rs748853352 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8924660 | GACTCCAAAGTTCAC[C/T]AACAACTGAGTTCTC | 7874 |
rs748881505 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8946876 | ACTGTATAATAAAAT[A/G]TATCAACATTTAGCA | 7874 |
rs748893272 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8959357 | CAAAACACTAATTCA[-/A]AAAAAAAAAAAAAGG | 7874 |
rs748897154 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8919079 | TAGCAGGCTGTTCAT[A/G]TAACAAGTCGCTCCC | 7874 |
rs748943439 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8955705 | GCACGATTCCATCTC[-/A]AAAAAAAAAAAAAAA | 7874 |
rs748969083 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956542 | GGCGGAGGCGGGCAG[A/G]CTGCCTGAGCTCAGG | 7874 |
rs749014851 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8899688 | GAAAATGACATCAAC[A/G]CGGTGGTAGAGATCT | 7874 |
rs749018741 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8953076 | CCCTGACCTCGTAAT[A/C]TGTCGCCTTGGCCTC | 7874 |
rs749029458 | snp | A/C | 0.000201244 | 0.010029 | intron-variant | USP7 | GRCh38.p7 | 16:8930246 | ATCTGAACCTGTTTT[A/C]TGACAAGTTTCCGCC | 7874 |
rs749036509 | snp | C/T | 1.69945e-05 | 0.00291496 | intron-variant | USP7 | GRCh38.p7 | 16:8900968 | AGAATATACTAATTA[C/T]GGAAAAATAAACCAT | 7874 |
rs749042554 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8942982 | CTTTTCAGGCACTGC[A/G]GGCCCTGAGGTCAGC | 7874 |
rs749087044 | in-del | -/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8936052 | CCCAAAAAGCTGGCA[-/G]GGGGCGGGGGTCGCG | 7874 |
rs749094262 | snp | A/T | 1.65064e-05 | 0.00287279 | intron-variant | USP7 | GRCh38.p7 | 16:8916478 | TTCATTGTAAGAAAT[A/T]TACAAGTATTGCTTG | 7874 |
rs749102250 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8920038 | TCATCAAAGTAACAA[A/C]GGAGCATCTCTGCTC | 7874 |
rs749138865 | snp | A/G | 3.29457e-05 | 0.00405854 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8923283 | TGGTCTGTCTGGATA[A/G]AAGCGTGGCATCACC | 7874 |
rs749201358 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8905578 | TGTGGGCACTGCTAC[A/C]ATTCGCCCAATGGCA | 7874 |
rs749212015 | in-del | -/A | 1.6585e-05 | 0.00287962 | splice-donor-variant | USP7 | GRCh38.p7 | 16:8915251 | ATACACACAACACTT[-/A]ACTATTTTTCTTTCC | 7874 |
rs749221448 | snp | A/C | 1.92291e-05 | 0.00310067 | intron-variant | USP7 | GRCh38.p7 | 16:8902498 | CTGAAAAAAATATTA[A/C]GAGTAGATTAAAATA | 7874 |
rs749245139 | snp | C/G | 1.65408e-05 | 0.00287578 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8894605 | GTCTTCATTTATGTA[C/G]TGGTGTCGGCCCATC | 7874 |
rs749249047 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8939227 | TCCAACACCACAAGG[A/T]TCCCTCCAGTGGCCC | 7874 |
rs749254297 | in-del | -/TTAAAAAG | | | intron-variant | USP7 | GRCh38.p7 | 16:8912860 | AAAATAAAAAAAAAT[-/TTAAAAAG]TTTGAAAATGAAACA | 7874 |
rs749310485 | snp | C/T | 1.87187e-05 | 0.00305925 | intron-variant | USP7 | GRCh38.p7 | 16:8898683 | TGACTTGTTTATTTG[C/T]CTAAAAACAAATATC | 7874 |
rs749318628 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8949531 | TTTCATCCACCCAGA[A/G]GCCTTGCCGCTGCCA | 7874 |
rs749370564 | snp | C/G | 1.66776e-05 | 0.00288765 | intron-variant | USP7 | GRCh38.p7 | 16:8910858 | GAGAAAAGTCAAGTG[C/G]TAAAGCTTCATTTAT | 7874 |
rs749385823 | snp | C/T | 1.65814e-05 | 0.00287931 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8921261 | CTCTGTAATTTATTA[C/T]CTTCAGCACTGCTTG | 7874 |
rs749400495 | snp | A/G | 0.00011689 | 0.00764403 | intron-variant | USP7 | GRCh38.p7 | 16:8903237 | GACGTTGGGAGCCAC[A/G]GTGGGGTATATCCAC | 7874 |
rs749401094 | snp | A/G | 1.64776e-05 | 0.00287028 | intron-variant | USP7 | GRCh38.p7 | 16:8902074 | GCAGGCGTCTCGTGG[A/G]CACTTACGATCTTTA | 7874 |
rs749402935 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8959483 | GGAGCCTGGGGAATC[C/G]CTTTGAATCATTAAA | 7874 |
rs749508631 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8913637 | AAACTCATCTCAGCC[A/G]ACCCGCACTAAATGA | 7874 |
rs749516000 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8951093 | ATGTTTATTTCTACT[A/T]TCTTCGATCAGTGAC | 7874 |
rs749520277 | snp | C/T | 1.6476e-05 | 0.00287014 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893986 | CTCGCCTTGAACACA[C/T]CAGCTTGGAAATCAG | 7874 |
rs749532670 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8903685 | CCAGCCTGACCAACA[C/T]GGAGAAACCCTGTCT | 7874 |
rs749543080 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8902843 | CAGTGAGCCAAGATC[C/G]CGCCACTGGGCAACA | 7874 |
rs749555917 | snp | C/T | 1.67984e-05 | 0.00289809 | intron-variant | USP7 | GRCh38.p7 | 16:8900644 | TCCTACAGTGAAAGA[C/T]ATAAAATTGTTACAC | 7874 |
rs749558329 | snp | A/G | 1.68584e-05 | 0.00290326 | intron-variant | USP7 | GRCh38.p7 | 16:8901278 | AGATCCAAACACTCA[A/G]CACAATGCTTAAAAA | 7874 |
rs749565834 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8932801 | GGATGGACAAAGCAG[A/G]ATAGTGCCTTATCTG | 7874 |
rs749568892 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8900744 | TTCTATCCACCTTTT[-/A]AAGTTAAAATGTTAA | 7874 |
rs749570604 | in-del | -/CTG | 0.0110893 | 0.0736319 | cds-indel, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8963256 | CTGCTCGCCCGCTTT[-/CTG]CTGCTGCTGCTGCTG | 7874 |
rs749584922 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8900097 | TGGTGGAGCCCAGTC[C/T]CTGACCGTGAGTCAG | 7874 |
rs749591822 | snp | A/G | 3.29777e-05 | 0.00406051 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8904456 | TTGCATATAGAGATG[A/G]GCTTCCTGCCGCTCC | 7874 |
rs749661550 | snp | C/T | | | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8899156 | CAGCAACATTGGATC[C/T]GTGTTGAGCCTCTGT | 7874 |
rs749681743 | snp | G/T | 1.67835e-05 | 0.0028968 | intron-variant | USP7 | GRCh38.p7 | 16:8904388 | GTGTATAGAGATGGG[G/T]GCCCGGCTGCATGGT | 7874 |
rs749699589 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8932144 | AATAAAATGGTACTC[C/T]CCACCACCCAAGCAT | 7874 |
rs749784172 | in-del | -/GTC | | | intron-variant | USP7 | GRCh38.p7 | 16:8926748 | TCCAATCTGCCTGGA[-/GTC]TGCCACTAACATTAG | 7874 |
rs749791558 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8940783 | GCTGGCTTCAGGTAG[A/G]GCCCTGGAATATTAG | 7874 |
rs749797705 | in-del | -/G | 1.85266e-05 | 0.00304351 | intron-variant | USP7 | GRCh38.p7 | 16:8898682 | ATGACTTGTTTATTT[-/G]CCTAAAAACAAATAT | 7874 |
rs749841392 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8908196 | ATTCCTTTAACACTG[C/T]GGCTCTTGGGACACA | 7874 |
rs749864016 | snp | A/G | 1.65233e-05 | 0.00287426 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8899143 | ACTTGAAAAACTGCA[A/G]CAACATTGGATCTGT | 7874 |
rs749871353 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8918081 | AGGCATGAGCCACTG[C/T]GCCCAGCCATGGAGC | 7874 |
rs749876464 | in-del | -/ATA | | | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964801 | TCTCAACTAATAGTG[-/ATA]ATAAAATAATAATAT | 7874 |
rs749891129 | snp | C/T | 1.65059e-05 | 0.00287275 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8921158 | ACACTGTTACTTACA[C/T]TCCAGGCCATAAAAT | 7874 |
rs749893609 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8949110 | GTCACACAATTGTGA[A/C]TACTAAAAACCACTG | 7874 |
rs749894577 | snp | A/G | 3.30175e-05 | 0.00406296 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8910825 | CCACAAATGATTCAA[A/G]TACTTTAAAGAGAGA | 7874 |
rs749899601 | snp | A/G | 1.75317e-05 | 0.00296067 | intron-variant | USP7 | GRCh38.p7 | 16:8898655 | CTACACAAGAAAACA[A/G]CATATAAATAAATGA | 7874 |
rs749959927 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892769 | TCCACGTAACTCACT[C/G]AATTATAATTTTTAT | 7874 |
rs749981537 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8958905 | TGCTTAGGCAGAGGC[C/T]GGATGGCTTCTTCCT | 7874 |
rs749984635 | snp | C/T | 3.5512e-05 | 0.00421364 | intron-variant | USP7 | GRCh38.p7 | 16:8920487 | CAGCTTGAATAAGAA[C/T]ACACATTTTATTCCC | 7874 |
rs749994453 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8903067 | GCAAAATCCTGTGGG[C/T]TCCCCTGTGCAGGAG | 7874 |
rs750093857 | snp | C/G | 0.00769827 | 0.0615619 | missense, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8963274 | CTGCTGCTGCTGCTG[C/G]TGGTGGTTCATGTCG | 7874 |
rs750095581 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8925308 | ACACAGGCCTCAACA[A/C]AATGAGACTACTAGC | 7874 |
rs750112183 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8905263 | GTCGTCATCGTGACC[C/T]CCATAATTGTGCTCA | 7874 |
rs750130160 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8902537 | CTCATATTTTAGTCC[C/T]CTATATTACACACAC | 7874 |
rs750140318 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8912449 | GTGAGACTCCATGTC[-/A]AAAAAAAAAAAAAGA | 7874 |
rs750145582 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8901169 | ATATTGGTGTGTAGA[C/T]ATGCCCACAGTAATT | 7874 |
rs750170706 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950255 | ATGTTATCACTCAGA[A/G]CCTTGGTATCTAGGC | 7874 |
rs750184960 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8952449 | GGGCTAAAACCAAGG[C/T]GCCAGCAGGGCCACA | 7874 |
rs750206628 | snp | A/C | 1.73429e-05 | 0.00294468 | intron-variant | USP7 | GRCh38.p7 | 16:8930403 | GTATCTCCCGCTTTA[A/C]AGAAGAAAAAGAAAT | 7874 |
rs750214759 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8898898 | TGGGAGATGCACTGA[C/G]GATGTATCTAAAGTC | 7874 |
rs750218349 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8933028 | TCACTGCAACCTCTG[C/T]CTCCGGGGTGCCAGC | 7874 |
rs750221883 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8922287 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 7874 |
rs750227103 | snp | C/T | 4.9516e-05 | 0.00497549 | missense, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8930314 | CCATGTCCTCCTCCG[C/T]GGTGTTGTGTCCATC | 7874 |
rs750242895 | in-del | -/A | 1.672e-05 | 0.00289132 | intron-variant | USP7 | GRCh38.p7 | 16:8898347 | AAAATTCATAGTATT[-/A]AAAAAAACTTACCTC | 7874 |
rs750266512 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8912107 | GAATATCTAACACCC[-/A]AGCAAGATAAAAACC | 7874 |
rs750294959 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8908724 | GCCCAGCAATCAGGG[A/T]AGAAATGGTTAAGGA | 7874 |
rs750311423 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8931941 | TCTCAACTGCATACA[A/G]GAGATGTGCTTTTTA | 7874 |
rs750356506 | in-del | -/TCAT | | | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964952 | ATCTCCTGTCCTGTC[-/TCAT]TCAGTCATTGACAGA | 7874 |
rs750384591 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8907799 | AGCCTGGGCGACACA[C/G]CAAGACTCTGTCTCA | 7874 |
rs750387597 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8940507 | GGGCAGGGGTTACCT[C/T]GGGACCAGGCAACCC | 7874 |
rs750390005 | snp | A/G | 3.29495e-05 | 0.00405877 | intron-variant | USP7 | GRCh38.p7 | 16:8894778 | CAGGAGGCCCCAGCT[A/G]CACACCTTCTCAAAC | 7874 |
rs750397843 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8918806 | AGAGCAAGACTCCAT[C/T]TCAATAAAGAAAAAG | 7874 |
rs750404372 | snp | C/T | 0.000105338 | 0.00725658 | intron-variant | USP7 | GRCh38.p7 | 16:8902523 | AAAATAAAAACACGC[C/T]CATATTTTAGTCCTC | 7874 |
rs750439046 | snp | C/T | 1.64882e-05 | 0.00287121 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8903291 | GAGAGAGGCTCTGAA[C/T]AAACTCAGCAAGCGA | 7874 |
rs750444238 | in-del | -/TCTT | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957992 | TATGGCTTCAGCGTC[-/TCTT]TCTCAGAGCCACTTG | 7874 |
rs750449021 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8951744 | AAATCTCTCCATACA[C/G]TCAGATACATACAGC | 7874 |
rs750452519 | snp | A/G | 5.05898e-05 | 0.00502915 | intron-variant | USP7 | GRCh38.p7 | 16:8915206 | GAAACATTAAAACAC[A/G]GTAGAAATCATCAAA | 7874 |
rs750455005 | snp | C/T | 1.65932e-05 | 0.00288034 | intron-variant | USP7 | GRCh38.p7 | 16:8899561 | AAAGAAATTTGTCTT[C/T]CTGGAGTGGGATCTG | 7874 |
rs750461366 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8945618 | GTGGGAGACAGCACA[A/G]TAAAGATGTTCTCCC | 7874 |
rs750484242 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8929345 | CAGGTAACAAAGCAG[C/T]GGGTTTAGACCACGC | 7874 |
rs750513359 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8894902 | TCACTCCCAGCACCC[C/T]CAGGCCACGTCACGT | 7874 |
rs750517814 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8906078 | AAGGTAGGACCAGGG[G/T]GCACGCAGAGGGACA | 7874 |
rs750518112 | snp | C/T | 4.94246e-05 | 0.0049709 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8923349 | AGGGCTAAGGACCGA[C/T]TCACTCAGTCTGCTG | 7874 |
rs750525128 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8897988 | ACTAGCAGCTTGGGG[-/A]GTAAGCGCAGAGTCA | 7874 |
rs750527203 | in-del | -/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8949123 | AATACTAAAAACCAC[-/T]TGAACCCACTTTAAA | 7874 |
rs750535910 | snp | A/G | | | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962203 | AAGCAAAACTAAAGC[A/G]TTCCACGCCGTTTTC | 7874 |
rs750583654 | in-del | -/AAC/AC | 0.000288386 | 0.0120049 | intron-variant | USP7 | GRCh38.p7 | 16:8916982 | CTAAAAAAAAAAAAA[-/AAC/AC]AAAAGAGGAAGCAGA | 7874 |
rs750626744 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938236 | TAACCTGGATTCCTG[C/T]AGGACTGCTACTACA | 7874 |
rs750643787 | snp | A/G | 1.65674e-05 | 0.00287809 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8894563 | ACCGGGCTGTGGCTC[A/G]AAGTCTTTCAAATTT | 7874 |
rs750660777 | in-del | -/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8929035 | TGTCTCCTCCCAAGA[-/C]CCTCCCCCCTAAAAA | 7874 |
rs750686047 | snp | C/T | 2.14751e-05 | 0.00327675 | intron-variant | USP7 | GRCh38.p7 | 16:8906613 | TTAAAAGAAATTCAG[C/T]ATTAATTTACACAAA | 7874 |
rs750697886 | snp | A/T | 0.000123037 | 0.0078424 | intron-variant | USP7 | GRCh38.p7 | 16:8915562 | TTAAAAAAACTTTTT[A/T]GTACTTAGTAATATA | 7874 |
rs750714056 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8904665 | AATAATCTATTAGGC[C/T]GGCGTGGTGGCTTAC | 7874 |
rs750769477 | snp | G/T | 1.6486e-05 | 0.00287102 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8895650 | CAGATACCTCTATTC[G/T]AAACGTCCGGCTCGT | 7874 |
rs750769550 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8934592 | AGGGCTTCTCTGCAG[C/T]TGGCCTTGAAAACGC | 7874 |
rs750795213 | snp | C/T | 1.8085e-05 | 0.00300702 | utr-variant-5-prime, intron-variant | USP7 | GRCh38.p7 | 16:8936691 | AGTGACTGCATAGAA[C/T]CTCTAGGAGCTCTAC | 7874 |
rs750796767 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8911895 | GAGCTCACGACAGGC[C/T]GGGAAGTCTGTGTTC | 7874 |
rs750805202 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8909921 | ACAGACCGAGTCTCC[A/G]TCTCAGAAAAAAAAG | 7874 |
rs750857096 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8943578 | GGCTCCACCTCCCTC[A/G]TTAACGTGGGATACC | 7874 |
rs750926675 | in-del | -/T | 1.65176e-05 | 0.00287376 | splice-acceptor-variant | USP7 | GRCh38.p7 | 16:8910828 | AAATGATTCAAATAC[-/T]TTTAAAGAGAGAGAG | 7874 |
rs750930936 | snp | G/T | 1.64942e-05 | 0.00287173 | intron-variant | USP7 | GRCh38.p7 | 16:8895196 | TAAGTGCAAGTGATG[G/T]GGTCAAAGTGTCCAC | 7874 |
rs750953463 | snp | A/C | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8899642 | ATAACGTAACCACAA[A/C]TCCAGGATCATTAGG | 7874 |
rs750962138 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8930492 | TGATGTTGCCTAATC[A/G]TTAATAAATTCCAAT | 7874 |
rs751022644 | snp | C/G | 1.64822e-05 | 0.00287068 | intron-variant | USP7 | GRCh38.p7 | 16:8894901 | GTCACTCCCAGCACC[C/G]CCAGGCCACGTCACG | 7874 |
rs751026073 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8924327 | TAAAGCATCATGAAA[C/T]TGCCACAGCAAAGTC | 7874 |
rs751026731 | snp | A/G | 3.29679e-05 | 0.00405991 | intron-variant | USP7 | GRCh38.p7 | 16:8915365 | AATAAGGAAAGTAAA[A/G]GTGGTTTAACTAGTA | 7874 |
rs751027543 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8908975 | TGCATAAGAACCCAT[A/G]TATCACAGGGCACGC | 7874 |
rs751075551 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8919756 | CTCCCACCTCCACGC[A/C]CATCTCCCTCTGTAC | 7874 |
rs751093341 | in-del | -/AT | | | intron-variant | USP7 | GRCh38.p7 | 16:8924039 | GGTATTTTTTCCCAC[-/AT]GAGTAGTATAAATTG | 7874 |
rs751107614 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8940640 | GGCAGCCAAAAAAGA[C/T]GGAGTTACCACACTC | 7874 |
rs751108261 | snp | A/G | 1.7612e-05 | 0.00296744 | intron-variant | USP7 | GRCh38.p7 | 16:8921339 | TTGACATTATTTACC[A/G]GATGTTATACATTTT | 7874 |
rs751135164 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893763 | CTTGCACTGTGGTTA[C/T]CATAAAATAACTCTC | 7874 |
rs751143265 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8952702 | ATTTGCAGGTTTCAG[C/T]GATTAGGACATGGAC | 7874 |
rs751183254 | snp | C/T | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8894819 | GGATGTCCAGCAGGC[C/T]CTGGATTCGCTTCAT | 7874 |
rs751183334 | snp | C/T | 1.65053e-05 | 0.0028727 | intron-variant | USP7 | GRCh38.p7 | 16:8899111 | GCAAGTGTCCACACA[C/T]GTGACCTACCCTTGA | 7874 |
rs751195827 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8949293 | TGGCATTTAACATCG[C/T]GGCACGTTCCACTGG | 7874 |
rs751217208 | snp | C/T | 1.64871e-05 | 0.00287111 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8921181 | CATAAAATTGGAAAA[C/T]CCCCAATCATTTTCT | 7874 |
rs751231306 | snp | C/T | 4.95037e-05 | 0.00497488 | intron-variant | USP7 | GRCh38.p7 | 16:8902204 | TATTTCCAAAAGAGA[C/T]GCTGATTTTAGAAGA | 7874 |
rs751273206 | snp | C/T | 1.79361e-05 | 0.00299462 | intron-variant | USP7 | GRCh38.p7 | 16:8898668 | CAGCATATAAATAAA[C/T]GACTTGTTTATTTGC | 7874 |
rs751285052 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8927405 | GAAATTTCTCCAAAT[A/G]GTGCTGTTGCAGTGA | 7874 |
rs751315087 | snp | C/T | 0.000125149 | 0.0079094 | intron-variant | USP7 | GRCh38.p7 | 16:8936565 | GCATAAGGAGCTCAA[C/T]CTGAAAACCTGACTC | 7874 |
rs751340963 | snp | C/G | 3.29766e-05 | 0.00406045 | intron-variant | USP7 | GRCh38.p7 | 16:8919157 | GAAAGATCAGTTCAA[C/G]GTTGAGGGGATCTTG | 7874 |
rs751354759 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956973 | CCAGACACCCCTCTG[C/T]CCATCCCATGCTGGG | 7874 |
rs751360755 | snp | G/T | 0.000132087 | 0.00812565 | intron-variant | USP7 | GRCh38.p7 | 16:8901061 | GGAGCAAGTCACCTA[G/T]GAGAAAGAAGATATT | 7874 |
rs751370808 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8914289 | TGACAGCTCCAGTGT[A/G]GGTGTGGAGCAACTG | 7874 |
rs751413670 | in-del | -/CAA | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957735 | GCACTACAGCCAGAG[-/CAA]CAGAGCAAGACCCTG | 7874 |
rs751433015 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8923098 | GTGGGTTTTAAAGAG[A/C]AACACGTATTTAATC | 7874 |
rs751448471 | snp | C/G | | | utr-variant-5-prime, intron-variant | USP7 | GRCh38.p7 | 16:8956331 | TGGGCCACAGCGCTC[C/G]CTCCCAGGTTTCAAA | 7874 |
rs751520234 | snp | C/T | 3.45155e-05 | 0.0041541 | intron-variant | USP7 | GRCh38.p7 | 16:8900675 | TGCAAGTTTGTCTAA[C/T]GTTTAATATGGCCAG | 7874 |
rs751550271 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8954621 | GAGATGAAGACTTGC[C/G]AAAAACTTTACTAAC | 7874 |
rs751552064 | snp | C/T | 3.29582e-05 | 0.00405931 | intron-variant | USP7 | GRCh38.p7 | 16:8899798 | CTGAATCAAAGTCCA[C/T]GGCAGGGGGTAGCTG | 7874 |
rs751606844 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8921650 | AGCCCTTCAGTGCCA[C/T]GCCTCTCGAGCTCTC | 7874 |
rs751616912 | snp | A/G | 1.66335e-05 | 0.00288383 | intron-variant | USP7 | GRCh38.p7 | 16:8904420 | ACCCGGAGTCCCAGA[A/G]GGGCGGGGGCTGACC | 7874 |
rs751673975 | snp | A/C | 1.65116e-05 | 0.00287324 | intron-variant | USP7 | GRCh38.p7 | 16:8916593 | ACTCCATTTAAAGCT[A/C]AACTTTCAAATGAGC | 7874 |
rs751686417 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8965286 | CGCGGTGGCTCACAC[C/T]TGTAATCCCAGCACT | 7874 |
rs751692484 | snp | C/T | 0.000185856 | 0.00963813 | intron-variant | USP7 | GRCh38.p7 | 16:8929581 | GAGGATTGATGGACA[C/T]GCTTTTTGACAGAAC | 7874 |
rs751693433 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8907757 | AGTTCAAGGCTGCAG[A/T]GAGCCATGATCATGC | 7874 |
rs751705510 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8952972 | CTCCCAAGTAGCTGG[A/G]ATTACAGTCGCGTGT | 7874 |
rs751732496 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8929669 | CCCTACTCACAAGTG[G/T]GACTGTGCAAATATT | 7874 |
rs751756032 | snp | A/C/G | 4.97528e-05 | 0.00498742 | intron-variant | USP7 | GRCh38.p7 | 16:8903259 | TATATCCACGGGACC[A/C/G]GTACGCACCATGGTC | 7874 |
rs751760913 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8907440 | AAACCTGAAGGCTGA[A/G]TGACCAACCTATATT | 7874 |
rs751779867 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8910379 | AAAATACATTTAAAA[A/C]TAAAGAAACACAACC | 7874 |
rs751785158 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8899675 | TTGTTTTATCACAGA[A/G]AATGACATCAACGCG | 7874 |
rs751786218 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8896318 | AAAGTTGCATAAACC[A/T]TTCCCACAAGGAATT | 7874 |
rs751807715 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8939770 | AGTTTAATAACTCCA[A/T]AACATTGTCATGATT | 7874 |
rs751850015 | snp | C/G | 1.67629e-05 | 0.00289503 | intron-variant | USP7 | GRCh38.p7 | 16:8903218 | GTGACACGGAAGGAA[C/G]GTGGACGTTGGGAGC | 7874 |
rs751871193 | snp | C/T | 1.64814e-05 | 0.00287061 | intron-variant | USP7 | GRCh38.p7 | 16:8910740 | GCACAAAACACTCAA[C/T]TTACCTGTAAGCCAT | 7874 |
rs751887662 | snp | A/G | 6.59772e-05 | 0.00574319 | intron-variant | USP7 | GRCh38.p7 | 16:8902065 | TAAGTGCAGGCAGGC[A/G]TCTCGTGGGCACTTA | 7874 |
rs751912433 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961326 | GGAGAAACCCCGTCT[C/G]TAACAAAAATACAAA | 7874 |
rs751982165 | in-del | -/AG | 0.42 | 0.183303 | intron-variant | USP7 | GRCh38.p7 | 16:8910834 | ATTCAAATACTTTAA[-/AG]AGAGAGAGAGAAAAG | 7874 |
rs751983501 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8941139 | CCCATGCCCCATGCC[C/T]ATGAGGACCCCCCGC | 7874 |
rs751996046 | snp | A/G | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894098 | GGCCGAGGATGAGAC[A/G]TATTACCTGGTGGGG | 7874 |
rs752021202 | snp | A/T | 0.000131878 | 0.00811922 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8895656 | CCTCTATTCGAAACG[A/T]CCGGCTCGTTGCAGG | 7874 |
rs752029401 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8922108 | CCCAAATACTCATCA[A/G]ATCACATCATAATGT | 7874 |
rs752049957 | snp | A/C | 1.64789e-05 | 0.0028704 | intron-variant | USP7 | GRCh38.p7 | 16:8905177 | CAGAACAAAAGTGAA[A/C]ACTACTCACTCAGTT | 7874 |
rs752072635 | in-del | -/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8942095 | GAGCAAACCGCAACA[-/G]GAACAGGAACAGGGC | 7874 |
rs752081528 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8911975 | CAACTGAAAGGATGT[A/G]GGGACAGGTTATCCC | 7874 |
rs752086665 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8954793 | GTAAAACCCCCCCTC[C/T]ACTAAAGATACAAAA | 7874 |
rs752100552 | snp | C/T | 1.64803e-05 | 0.00287052 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893971 | CACCCACACACCGTC[C/T]TCGCCTTGAACACAC | 7874 |
rs752149478 | snp | G/T | 3.29538e-05 | 0.00405904 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8917109 | TTGTAATGCTAAAGG[G/T]ACGCTTTTAGACGAA | 7874 |
rs752156575 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8922019 | CTCGGGACGCTGACA[A/C]TGGGTATGGACCATT | 7874 |
rs752174551 | snp | C/G | 3.31779e-05 | 0.00407282 | intron-variant | USP7 | GRCh38.p7 | 16:8904426 | AGTCCCAGAAGGGCG[C/G]GGGCTGACCTGCACT | 7874 |
rs752181569 | snp | A/C | 1.64841e-05 | 0.00287085 | missense, intron-variant | USP7 | GRCh38.p7 | 16:8904548 | TATCATGGTCGGTGA[A/C]CGCCTGTAAAACTTC | 7874 |
rs752219394 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8942386 | CACCCTTATCACATG[C/G]TAGGGGTCTCCTGAC | 7874 |
rs752244531 | snp | A/G | 3.5603e-05 | 0.00421903 | splice-donor-variant, intron-variant | USP7 | GRCh38.p7 | 16:8936581 | CTGAAAACCTGACTC[A/G]CCTTCCAGCCCAAGC | 7874 |
rs752285038 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8895064 | AAACGGGATTCCGAA[C/T]GTTCCGAAGACCTCT | 7874 |
rs752289044 | in-del | -/GG | 0.00150844 | 0.0274216 | intron-variant | USP7 | GRCh38.p7 | 16:8916989 | AAAAAAAAAAAAAGA[-/GG]AAGCAGAATGGCAAA | 7874 |
rs752301571 | snp | C/G | 1.66685e-05 | 0.00288686 | intron-variant | USP7 | GRCh38.p7 | 16:8899230 | TTTTGGGGAAAAATT[C/G]AAACTTGGTCATAAA | 7874 |
rs752309675 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950835 | CTGAGCGGGCACTAT[C/T]TGTCACTTGTTTCTG | 7874 |
rs752317217 | in-del | -/C/T | 0.000561996 | 0.0167548 | intron-variant, frameshift-variant | USP7 | GRCh38.p7 | 16:8894532 | ACACCAGCCCCCGGG[-/C/T]GGGGGGAGAACCCTT | 7874 |
rs752392170 | snp | C/T | 4.94743e-05 | 0.0049734 | intron-variant | USP7 | GRCh38.p7 | 16:8915379 | AAGTGGTTTAACTAG[C/T]AATAGTCAAAAAATT | 7874 |
rs752406278 | snp | G/T | 1.64757e-05 | 0.00287012 | intron-variant | USP7 | GRCh38.p7 | 16:8894985 | AGCGGCCACTCAAAG[G/T]CTCCAGGTTTTGACG | 7874 |
rs752417268 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8919799 | CCTGAACACACGACC[A/G]TCACCAAGCGGGACC | 7874 |
rs752426274 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8916481 | ATTGTAAGAAATATA[C/T]AAGTATTGCTTGAAA | 7874 |
rs752435427 | snp | A/G | 1.65723e-05 | 0.00287852 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8908420 | GTAACACTGGTGGCA[A/G]TGTTAGGAATTTCAC | 7874 |
rs752462798 | snp | A/T | 1.6641e-05 | 0.00288448 | intron-variant | USP7 | GRCh38.p7 | 16:8920345 | TAACAGCACCTGATT[A/T]AAGAAAAACTTACGC | 7874 |
rs752495266 | snp | A/C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8948374 | TTTTTTTGTAGAGAC[A/C/G]AGTTTTCACCATGTT | 7874 |
rs752533717 | in-del | -/AAGT | | | intron-variant | USP7 | GRCh38.p7 | 16:8918391 | TAAAATTTTCAATAA[-/AAGT]AAGTTGCATTGACTT | 7874 |
rs752572345 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8925165 | GAGGAAATGGAGGTT[C/T]GCCGAGGCTGTTTTA | 7874 |
rs752622683 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8915768 | ATAAATTAGTAATCT[A/G]TAGTGCCTTTAGAAG | 7874 |
rs752636299 | snp | A/G | | | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8895712 | TCTTGATGAACACCA[A/G]TGATTTTGTAGCTTA | 7874 |
rs752660336 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8934468 | ATCTTACAGGATGGG[G/T]TGGGGGAAATGCGTA | 7874 |
rs752665247 | snp | A/G | 0.000379016 | 0.013761 | intron-variant | USP7 | GRCh38.p7 | 16:8918993 | CTGAGAAGAAAGGGT[A/G]AGCGGAAGGCTGCAG | 7874 |
rs752688663 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8947726 | CAAAAGCTCTTTAAG[A/G]GGTGAAGTCTTTTAG | 7874 |
rs752727742 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8945619 | TGGGAGACAGCACAG[G/T]AAAGATGTTCTCCCC | 7874 |
rs752733480 | in-del | -/C | 3.30437e-05 | 0.00406457 | intron-variant | USP7 | GRCh38.p7 | 16:8898480 | ATACCGTCACCAAAA[-/C]CCCCGAGCCTTCTCT | 7874 |
rs752759791 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8932813 | CAGGATAGTGCCTTA[C/T]CTGCGACATTTAAAG | 7874 |
rs752857703 | snp | A/G | 1.64792e-05 | 0.00287042 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8917122 | GGGACGCTTTTAGAC[A/G]AATCATCCCCCTCGG | 7874 |
rs752882692 | snp | A/C | 1.6549e-05 | 0.0028765 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8900540 | CATACTTCTGAAATA[A/C]TATGATGTCACCATC | 7874 |
rs752886943 | in-del | -/TTTACTGTTATTAACTGTT | 1.73546e-05 | 0.00294568 | intron-variant | USP7 | GRCh38.p7 | 16:8902372 | GATACGCTATTAACA[-/TTTACTGTTATTAACTGTT]ATATTTACTGTTTTA | 7874 |
rs752898341 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8897309 | CCAACCAAATACTGA[C/G]GGGAGGTTAACAAAA | 7874 |
rs752903044 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8922209 | AAAATGAAAGTACGG[C/G]CAGGTGCGCTGGCTC | 7874 |
rs752912851 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8898725 | ATAAAAGCAAACCGC[C/T]GGCCTTACACCTGGT | 7874 |
rs752927087 | in-del | -/TTTT | | | intron-variant | USP7 | GRCh38.p7 | 16:8903479 | AACACATTTAAACAC[-/TTTT]TAAAACGCTGAAAAC | 7874 |
rs752943752 | in-del | -/A | 0.375 | 0.216506 | intron-variant | USP7 | GRCh38.p7 | 16:8910846 | TAAAGAGAGAGAGAG[-/A]AAAGTCAAGTGCTAA | 7874 |
rs753015445 | snp | C/T | 1.65334e-05 | 0.00287514 | missense, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8930293 | ACCACAGGCACTTAC[C/T]ATCCTCCATGTCCTC | 7874 |
rs753022511 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8941368 | ACATATCCTGCAGTC[C/T]GCGGTTAACAACTTT | 7874 |
rs753040991 | in-del | -/TT | | | intron-variant | USP7 | GRCh38.p7 | 16:8896138 | GCCACCATGCCCAGC[-/TT]TTTTTTTTTTTTTTT | 7874 |
rs753042553 | snp | A/T | 0.000743771 | 0.01927 | intron-variant | USP7 | GRCh38.p7 | 16:8923165 | TAACTTAAGATAAAA[A/T]TGCACTAGGCTGATC | 7874 |
rs753064549 | snp | C/T | 1.65121e-05 | 0.00287329 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8899130 | ACCTACCCTTGAGAC[C/T]TGAAAAACTGCAGCA | 7874 |
rs753071325 | snp | C/T | 0.000101167 | 0.00711148 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8902392 | TTACTGTTTTATTGC[C/T]GTCGGCTTCATTATC | 7874 |
rs753123835 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8924798 | CAAAAGCATGTGTGA[C/G]GGTAAGCACTTCTAC | 7874 |
rs753139245 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8959224 | GTGCATTAGGTCCCA[C/T]AGCAATTAGATGGCA | 7874 |
rs753140433 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8903935 | AATAACTTAACTCAC[C/G]TATAAATTGGACCTA | 7874 |
rs753160107 | snp | A/G | 0.000247086 | 0.0111123 | intron-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894110 | GACATATTACCTGGT[A/G]GGGATGAAGAAAAGC | 7874 |
rs753170061 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8914097 | AGTTAAGGAAAAAGA[A/C]AAGAAGCCAATACTA | 7874 |
rs753196819 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8926507 | CAAGATAGGAGGGCC[-/A]AAAAAAAAGGAGAAG | 7874 |
rs753248157 | snp | C/T | 1.90532e-05 | 0.00308646 | intron-variant, missense | USP7 | GRCh38.p7 | 16:8894525 | TGAAACCCACACCAG[C/T]CCCCGGGGGGGGGAG | 7874 |
rs753249872 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8947563 | ATGTTGCCCAGGCTC[C/G]TCTCGAACTTCCGGC | 7874 |
rs753312745 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8925245 | GCACAGTGACCTGAC[A/T]CTGGTTTTTAAAATT | 7874 |
rs753320462 | snp | G/T | 1.65272e-05 | 0.0028746 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8906426 | GGTCCCACCACTTAC[G/T]TTGCCATCCCCTTTG | 7874 |
rs753341809 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957288 | TTTCTTAAGTCCAAA[C/T]TAGTTCAGAACAAGT | 7874 |
rs753346185 | snp | A/G | 3.29538e-05 | 0.00405904 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8901142 | GCACGAAGGACTTAC[A/G]TATTTTACAGGATAT | 7874 |
rs753348588 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8958118 | AAAAAGGAAACTGAG[A/G]TGGTCACCTTCAGAG | 7874 |
rs753389617 | snp | A/G | 0.00012119 | 0.00778334 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962562 | ACCTGGCCGGATGCT[A/G]GCTGCACCACACACT | 7874 |
rs753389669 | snp | C/T | 0.000115751 | 0.00760672 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8920379 | TCCATGGGGAGCATC[C/T]GCCTGTACAAAGACT | 7874 |
rs753406036 | snp | A/T | 8.37135e-05 | 0.00646914 | utr-variant-5-prime, intron-variant | USP7 | GRCh38.p7 | 16:8936672 | GTTCTCTCACCCACA[A/T]CAGAGTGACTGCATA | 7874 |
rs753507187 | snp | C/T | 1.65181e-05 | 0.00287381 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8903270 | GACCGGTACGCACCA[C/T]GGTCTGAGAGAGGCT | 7874 |
rs753532187 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8934038 | GCTGAGATTACAGGC[A/G]TGAAACACCACGCCT | 7874 |
rs753569794 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8911114 | ATACTGTAAAGCTAT[G/T]ATTATGAAGACAGCT | 7874 |
rs753575115 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8907521 | AATCAGATAAGGTAG[G/T]GCACATTGTCACTCC | 7874 |
rs753643150 | snp | A/C/T | 6.59004e-05 | 0.0057399 | intron-variant | USP7 | GRCh38.p7 | 16:8894770 | CAAGCCCCCAGGAGG[A/C/T]CCCAGCTGCACACCT | 7874 |
rs753664796 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8940402 | CTCAGGAGAACTCTT[C/T]GGCTTCTTGAACACA | 7874 |
rs753750730 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8939821 | AAGACTGTTTCTGGC[C/G]GAGCGCAGTGGCTCA | 7874 |
rs753792513 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8916690 | CTGTGAAGATTATTT[A/T]TGGGAGTCATAATTC | 7874 |
rs753793575 | snp | C/T | 4.2123e-05 | 0.00458909 | intron-variant | USP7 | GRCh38.p7 | 16:8906610 | ATTTTAAAAGAAATT[C/T]AGTATTAATTTACAC | 7874 |
rs753806744 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8926002 | TACCAAAACTACAAA[A/G]AATTAGCCGGGTGCA | 7874 |
rs753823616 | snp | A/G | 6.60884e-05 | 0.00574803 | intron-variant | USP7 | GRCh38.p7 | 16:8898471 | TTCACATCAGATACC[A/G]TCACCAAAACCCCGA | 7874 |
rs753862402 | snp | G/T | | | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891930 | GGAGAGGACACAATA[G/T]TCCCAGGGGTTACAG | 7874 |
rs753866155 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938135 | AGGCAGGAAGAATGG[A/C]AAAGTCCTGAGCAAA | 7874 |
rs753869740 | snp | A/G | 1.75237e-05 | 0.00295999 | intron-variant | USP7 | GRCh38.p7 | 16:8920480 | GAATATCCAGCTTGA[A/G]TAAGAACACACATTT | 7874 |
rs753872123 | snp | C/T | 8.82418e-05 | 0.00664177 | intron-variant, synonymous-codon | USP7 | GRCh38.p7 | 16:8894527 | AAACCCACACCAGCC[C/T]CCGGGGGGGGGAGAA | 7874 |
rs753877470 | in-del | -/AA | | | intron-variant | USP7 | GRCh38.p7 | 16:8902497 | CCTGAAAAAAATATT[-/AA]GAGTAGATTAAAATA | 7874 |
rs753887425 | snp | A/G | 1.64765e-05 | 0.00287019 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8919121 | GCCGACGTAGCCTGT[A/G]TGCTTCTTTGAATCC | 7874 |
rs753902498 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960822 | TTTCAGGATTGGGAA[A/G]GCTGAAATAGATGGC | 7874 |
rs753950856 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8904178 | GTCCCGGTTTGTGTA[A/T]CAGGAACTACTCTGG | 7874 |
rs753964068 | snp | C/T | 0.000164919 | 0.00907921 | intron-variant | USP7 | GRCh38.p7 | 16:8915382 | TGGTTTAACTAGTAA[C/T]AGTCAAAAAATTCAC | 7874 |
rs753971593 | snp | C/T | 1.65078e-05 | 0.00287291 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8906434 | CACTTACTTTGCCAT[C/T]CCCTTTGGGGTTTAG | 7874 |
rs753985008 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8936925 | AAACACTGTATCAAA[A/C]ACTGGTGATATAAAT | 7874 |
rs754032861 | snp | A/G | 1.64757e-05 | 0.00287012 | intron-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894116 | TTACCTGGTGGGGAT[A/G]AAGAAAAGCAAGTGA | 7874 |
rs754057602 | in-del | -/G | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957351 | TCTGTCATGGTACAT[-/G]GGCAAGAAATATGTT | 7874 |
rs754058894 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8914192 | TGAAAAGGTAAGAAC[A/G]ACCTCACTGATCTTC | 7874 |
rs754064130 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950543 | GAGAACACTGAAGAC[-/TT]TGATCACTTGGGCTG | 7874 |
rs754073529 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8945750 | GAGTAGGTAAAACAA[C/T]TTTGAATAACACAGA | 7874 |
rs754131338 | snp | A/G | 4.94409e-05 | 0.00497172 | intron-variant | USP7 | GRCh38.p7 | 16:8918997 | GAAGAAAGGGTGAGC[A/G]GAAGGCTGCAGGAGA | 7874 |
rs754144696 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8922788 | TGTTTAAATGTTCCT[C/G]AAGTCAGAGGGCCAT | 7874 |
rs754149915 | snp | A/C/T | 3.40178e-05 | 0.00412407 | intron-variant | USP7 | GRCh38.p7 | 16:8900662 | AAAATTGTTACACTG[A/C/T]AAGTTTGTCTAACGT | 7874 |
rs754175139 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8924983 | AATCCTTTTGAGGAT[-/A]AGAAGTCTACTAAAA | 7874 |
rs754178330 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8895082 | TCCGAAGACCTCTTT[A/G]TGGAAATGCGCCACT | 7874 |
rs754191654 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8926609 | AGTGATGGAGATCTT[C/T]GCCCAAGAAAATAGT | 7874 |
rs754211240 | in-del | -/AAAAA | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892609 | CTAGTTAGAGGCTAA[-/AAAAA]AAAAAAAAAAAAAAA | 7874 |
rs754215738 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8919922 | CCTAACGGCCTTGTC[A/G]CCCCTCTTTACTCCT | 7874 |
rs754228166 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8910321 | CCCTAGAGAACACAC[C/T]ACTCATTCTAAAGTC | 7874 |
rs754229086 | snp | A/G | 1.64895e-05 | 0.00287132 | intron-variant | USP7 | GRCh38.p7 | 16:8915388 | AACTAGTAATAGTCA[A/G]AAAATTCACATTCTA | 7874 |
rs754248329 | snp | A/G | 9.88728e-05 | 0.00703041 | intron-variant | USP7 | GRCh38.p7 | 16:8894753 | TTGAGCCTATGGCCC[A/G]CCAAGCCCCCAGGAG | 7874 |
rs754262044 | snp | C/T | 1.64738e-05 | 0.00286995 | missense, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8923339 | CAAAACACGGAGGGC[C/T]AAGGACCGACTCACT | 7874 |
rs754265136 | in-del | -/CTCAAACTCCTGAC | | | intron-variant | USP7 | GRCh38.p7 | 16:8933157 | GTTGGTCAGACTGGT[-/CTCAAACTCCTGAC]CTCAAGTGATCCACC | 7874 |
rs754283544 | in-del | -/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8904175 | CAGTCCCGGTTTGTG[-/T]TATCAGGAACTACTC | 7874 |
rs754295639 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8951145 | CAAACCAAGTAAGGA[G/T]TTCTGTATTTAAAAC | 7874 |
rs754307510 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8928567 | ACTGCAGCTGGAAAA[C/T]GCTGCCCTCAGCTAC | 7874 |
rs754310656 | in-del | -/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8955215 | TTTCCGTATGGCTCG[-/T]TTTTTTTACATATTA | 7874 |
rs754387673 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8962023 | GACTATCCAATTACT[A/G]GAAGTAAGTTATTCT | 7874 |
rs754411012 | in-del | -/TG | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956793 | AAAAAAAAAAAACAC[-/TG]AATTTGCTTTACACA | 7874 |
rs754419900 | snp | A/C/T | 1.6621e-05 | 0.00288274 | intron-variant | USP7 | GRCh38.p7 | 16:8904424 | GGAGTCCCAGAAGGG[A/C/T]GGGGGCTGACCTGCA | 7874 |
rs754443161 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8905866 | TTAAACAGTGATGAA[C/T]GCTGCTGTTACACGC | 7874 |
rs754447710 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8901834 | ACGTGATTAGCACAG[A/C]ACAGCAGCTGAGACT | 7874 |
rs754506621 | snp | A/G | 1.64958e-05 | 0.00287187 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8900589 | TTTATCAAGAGACAC[A/G]TCATAGTCCTGAATT | 7874 |
rs754511141 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8941371 | TATCCTGCAGTCTGC[A/G]GTTAACAACTTTTTA | 7874 |
rs754514003 | snp | C/G | 3.2969e-05 | 0.00405998 | intron-variant | USP7 | GRCh38.p7 | 16:8894905 | CTCCCAGCACCCCCA[C/G]GCCACGTCACGTGGC | 7874 |
rs754555695 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8909054 | AGTGTCAGCAAGGCC[C/T]TTCCCCAGCTGACTG | 7874 |
rs754592472 | in-del | -/AGAGA | 1.65704e-05 | 0.00287836 | intron-variant | USP7 | GRCh38.p7 | 16:8910842 | ACTTTAAAGAGAGAG[-/AGAGA]AAAGTCAAGTGCTAA | 7874 |
rs754594841 | snp | G/T | 1.68032e-05 | 0.0028985 | intron-variant | USP7 | GRCh38.p7 | 16:8915223 | TAGAAATCATCAAAA[G/T]ATCATGCCATTAGAT | 7874 |
rs754599493 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8940656 | GGAGTTACCACACTC[A/C]CTAAGAAGCTCCTGA | 7874 |
rs754646361 | snp | G/T | 1.64879e-05 | 0.00287118 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8921200 | CAATCATTTTCTTTA[G/T]GGAAGAACAAATGAC | 7874 |
rs754682286 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8912919 | AACTAGACACTGCAG[G/T]CAATTAGTGAAGATC | 7874 |
rs754687512 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8949294 | GGCATTTAACATCGT[C/G]GCACGTTCCACTGGG | 7874 |
rs754707182 | snp | C/T | 1.65056e-05 | 0.00287272 | intron-variant | USP7 | GRCh38.p7 | 16:8899117 | GTCCACACATGTGAC[C/T]TACCCTTGAGACTTG | 7874 |
rs754746569 | snp | A/G | 2.18124e-05 | 0.00330238 | intron-variant | USP7 | GRCh38.p7 | 16:8906614 | TAAAAGAAATTCAGT[A/G]TTAATTTACACAAAA | 7874 |
rs754760540 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8915578 | GTACTTAGTAATATA[G/T]ACAGTAATTTTATAA | 7874 |
rs754797194 | snp | C/G | 8.94494e-05 | 0.00668706 | intron-variant, missense | USP7 | GRCh38.p7 | 16:8894531 | CCACACCAGCCCCCG[C/G]GGGGGGGAGAACCCT | 7874 |
rs754808713 | snp | A/G | 1.68505e-05 | 0.00290258 | intron-variant | USP7 | GRCh38.p7 | 16:8898324 | AATAAGCAAGTTCCA[A/G]TAAAAATTAAAATTC | 7874 |
rs754832529 | snp | G/T | 1.65007e-05 | 0.00287229 | intron-variant | USP7 | GRCh38.p7 | 16:8919170 | AAGGTTGAGGGGATC[G/T]TGCAGATACCCCATT | 7874 |
rs754850845 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8919034 | CTATCCATTTACCTT[C/T]CGTAGCTGATTCGTG | 7874 |
rs754870389 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8914294 | GCTCCAGTGTGGGTG[G/T]GGAGCAACTGCAACT | 7874 |
rs754886163 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8900141 | TCGTGTGCCATCGAG[C/G]CACTTTCAGACACTG | 7874 |
rs754887002 | snp | A/C | 0.000236044 | 0.0108612 | intron-variant | USP7 | GRCh38.p7 | 16:8936572 | GAGCTCAACCTGAAA[A/C]CCTGACTCACCTTCC | 7874 |
rs754900602 | snp | C/T | 1.81332e-05 | 0.00301102 | intron-variant | USP7 | GRCh38.p7 | 16:8930421 | AAGAAAAAGAAATTC[C/T]ACGGGTTTTACATTC | 7874 |
rs754913346 | snp | A/G | | | utr-variant-5-prime, intron-variant | USP7 | GRCh38.p7 | 16:8956339 | AGCGCTCGCTCCCAG[A/G]TTTCAAACATTCATG | 7874 |
rs754915162 | snp | C/T | 0.000346332 | 0.0131547 | intron-variant | USP7 | GRCh38.p7 | 16:8900941 | ACAAACAAAACCCTC[C/T]ACAAACTACTAAGAA | 7874 |
rs754995247 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8908335 | TTATATCCCACTATA[A/G]ATTACCTATCATTGA | 7874 |
rs755017755 | snp | A/G | 0.000115707 | 0.00760528 | intron-variant | USP7 | GRCh38.p7 | 16:8895596 | AATATGCAGCAGATG[A/G]GGCTCATGAATTCTC | 7874 |
rs755052186 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8954660 | AAGGTATGTATTCAT[C/T]TGAGGTTTGCGTAGT | 7874 |
rs755083611 | snp | A/G | 1.64773e-05 | 0.00287026 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8917112 | TAATGCTAAAGGGAC[A/G]CTTTTAGACGAATCA | 7874 |
rs755089770 | snp | G/T | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8905194 | CTACTCACTCAGTTT[G/T]GATTCCCTGATGTAG | 7874 |
rs755135696 | in-del | -/TTA | 1.65323e-05 | 0.00287505 | splice-acceptor-variant | USP7 | GRCh38.p7 | 16:8898438 | ATTTTCATCTTAAGC[-/TTA]TATTAAGAAAAGAAA | 7874 |
rs755142195 | snp | C/G | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8899679 | TTTATCACAGAAAAT[C/G]ACATCAACGCGGTGG | 7874 |
rs755146685 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8930743 | AGAGGCCAAGGCGGA[C/G]AGATCACCTGAGGCC | 7874 |
rs755173525 | snp | C/T | 1.65206e-05 | 0.00287403 | intron-variant | USP7 | GRCh38.p7 | 16:8916604 | AGCTCAACTTTCAAA[C/T]GAGCAAATTAAAAGT | 7874 |
rs755221500 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8920820 | CCTCTGCAAAAAGCA[A/G]CCAAAGTGAACTGAA | 7874 |
rs755249669 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8940145 | TCCTGTATTTTTGTG[A/G]CTCCAAATGATGCTC | 7874 |
rs755258092 | snp | A/G | 1.68792e-05 | 0.00290505 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8923406 | TGCCTCGGAGCGCCA[A/G]CTGGTGTCTGCAAAA | 7874 |
rs755267621 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8896340 | CAAGGAATTCACATT[C/G]AGCTGATAGTGGCGT | 7874 |
rs755269881 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961395 | TACTTGGGAGGCTGA[A/G]GCAGGAAAATCGCTT | 7874 |
rs755271173 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8892911 | AAATAAGAGTGATTT[C/G]CTGATTCTATTTTAC | 7874 |
rs755295700 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8898671 | CATATAAATAAATGA[C/T]TTGTTTATTTGCCTA | 7874 |
rs755314328 | snp | C/T | 1.64909e-05 | 0.00287144 | intron-variant | USP7 | GRCh38.p7 | 16:8902069 | TGCAGGCAGGCGTCT[C/T]GTGGGCACTTACGAT | 7874 |
rs755324899 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8927553 | GGCCGTATTTGCTCT[A/G]AAACTTCCTTGGTGG | 7874 |
rs755330821 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894100 | CCGAGGATGAGACAT[A/G]TTACCTGGTGGGGAT | 7874 |
rs755336658 | snp | C/T | 3.32231e-05 | 0.00407559 | intron-variant | USP7 | GRCh38.p7 | 16:8921107 | AAAAAGTTAAGGGAA[C/T]AACAAGCAGTAATGC | 7874 |
rs755338641 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8941214 | ACTGGATACCTGAAA[C/T]CTCTTGGAAGGAGCC | 7874 |
rs755395704 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8903189 | CTACCCCCAAAGGCA[A/G]TCAGTATTTTCTAGT | 7874 |
rs755413035 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8926409 | GCTTGAACCTGGGAG[A/G]TGGAGGTTGCACTGA | 7874 |
rs755466249 | in-del | -/TA | | | intron-variant | USP7 | GRCh38.p7 | 16:8933603 | TGCACACACTCACAC[-/TA]TGTGTATGCGCTATC | 7874 |
rs755471601 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8958444 | TCAGCAAGGCAGTGA[C/T]GGACAGAAGTCCTGT | 7874 |
rs755471877 | snp | A/C | 1.65446e-05 | 0.00287612 | intron-variant | USP7 | GRCh38.p7 | 16:8901238 | ACATTACATCATCTA[A/C]AAGGTTAATAAACAA | 7874 |
rs755483009 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8935624 | GATGAAAAACGTCTA[C/T]AGGAAATAAAGCAAT | 7874 |
rs755489752 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8899203 | CCTAAGACACAGAAA[G/T]GAAGGTTCACATTTT | 7874 |
rs755535518 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8901569 | CCACGGGAAGATTGC[A/G]CATGGTCTTGTGTCT | 7874 |
rs755550443 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8924639 | ATGTCATCCAACAAC[C/G]CTTCAGACTCCAAAG | 7874 |
rs755557736 | snp | A/G | 1.64792e-05 | 0.00287042 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893974 | CCACACACCGTCCTC[A/G]CCTTGAACACACCAG | 7874 |
rs755588601 | snp | C/T | 1.64857e-05 | 0.00287099 | synonymous-codon, intron-variant | USP7 | GRCh38.p7 | 16:8904549 | ATCATGGTCGGTGAC[C/T]GCCTGTAAAACTTCA | 7874 |
rs755640262 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8923644 | GTGCTAACCATACAC[C/T]TGCCATCCCTGTCAG | 7874 |
rs755661396 | snp | C/T | 8.60356e-05 | 0.00655823 | intron-variant | USP7 | GRCh38.p7 | 16:8900951 | CCCTCCACAAACTAC[C/T]AAGAATATACTAATT | 7874 |
rs755680758 | snp | C/T | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8897072 | GGTCCCGGACACACC[C/T]ATGCTTGTCTGGATA | 7874 |
rs755685857 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8935784 | TCCCTGGCTAGTTCC[A/T]GGGCCTATATTCCCA | 7874 |
rs755699330 | in-del | -/TGGGGGTTTGTAGTTGCATCATTTAAAC | 0.0011422 | 0.0238704 | intron-variant | USP7 | GRCh38.p7 | 16:8923208 | AGTAATGAAATACTG[-/TGGGGGTTTGTAGTTGCATCATTTAAAC]TCTTACGTGGAATCA | 7874 |
rs755706330 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8926322 | GTCTCTACTAAAAAT[A/T]AAAAAAATTAGCTGG | 7874 |
rs755706610 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938050 | GGGTAAGGCAGGGCA[A/G]AATATCCTCCCTATG | 7874 |
rs755721554 | snp | C/G | 3.55885e-05 | 0.00421817 | splice-donor-variant, intron-variant | USP7 | GRCh38.p7 | 16:8936582 | TGAAAACCTGACTCA[C/G]CTTCCAGCCCAAGCC | 7874 |
rs755730163 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8932743 | AACCAAGGACAGTGA[C/G]TGGCCCTAGAAAGTG | 7874 |
rs755749063 | snp | A/G | 3.31367e-05 | 0.00407029 | intron-variant | USP7 | GRCh38.p7 | 16:8904429 | CCCAGAAGGGCGGGG[A/G]CTGACCTGCACTTGC | 7874 |
rs755833008 | in-del | -/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8932837 | TTTAAAGATGAAAAA[-/T]TTTTAAGAAGTAACA | 7874 |
rs755848678 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892474 | CGGTGCAAGGACCAC[A/G]CCCACGATAGCGCCT | 7874 |
rs755854323 | in-del | -/T | 8.67882e-05 | 0.00658685 | intron-variant | USP7 | GRCh38.p7 | 16:8916999 | AAAGAGGAAGCAGAA[-/T]GGCAAAGGCAGATGT | 7874 |
rs755890043 | snp | A/C | | | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962311 | ACTTTGCTTTGTTTC[A/C]GTGAAATGGGTCGTG | 7874 |
rs755951506 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8945926 | ACAACAGCACTGATT[A/G]AGAAATCACATTACC | 7874 |
rs755963807 | snp | C/T | 3.38186e-05 | 0.00411195 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8902465 | GGGCCACAATCGAAT[C/T]TGATCTTGTGGAAAT | 7874 |
rs755989081 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8915810 | TTTTTACCTCTGTGG[A/G]AAAGCATGTAAAATT | 7874 |
rs755998936 | snp | C/G | 1.66051e-05 | 0.00288137 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8908426 | CTGGTGGCAATGTTA[C/G]GAATTTCACACCTTT | 7874 |
rs756000119 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8939204 | CCACAGTTAAGATCC[C/T]GAACAGTTCCAACAC | 7874 |
rs756009144 | snp | A/G | 1.6623e-05 | 0.00288292 | intron-variant | USP7 | GRCh38.p7 | 16:8920349 | AGCACCTGATTAAAG[A/G]AAAACTTACGCAACT | 7874 |
rs756039376 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8927217 | GTCCCAGCTGCCTGG[C/G]AGGCTGAGGCAGGAG | 7874 |
rs756139984 | snp | C/T | 8.02665e-05 | 0.00633457 | utr-variant-5-prime, intron-variant | USP7 | GRCh38.p7 | 16:8936666 | GGGGAGGTTCTCTCA[C/T]CCACATCAGAGTGAC | 7874 |
rs756155090 | snp | G/T | 1.64746e-05 | 0.00287002 | intron-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894113 | ATATTACCTGGTGGG[G/T]ATGAAGAAAAGCAAG | 7874 |
rs756166131 | in-del | -/TACC | 1.65217e-05 | 0.00287412 | intron-variant | USP7 | GRCh38.p7 | 16:8898527 | ATTAATTTGGACTCA[-/TACC]TACCTGCTGATAGTA | 7874 |
rs756184205 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8913521 | GTAGAACGTCTAACA[A/G]ACCGAAGGAAGGAAC | 7874 |
rs756184765 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8946842 | ATGTCTGGGCATATA[A/C]ACTCAACTTTTTAAT | 7874 |
rs756187298 | in-del | -/C | 1.64803e-05 | 0.00287052 | intron-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894137 | AAGCAAGTGAGGCCA[-/C]AGAGCAGCCCTGGAA | 7874 |
rs756196308 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8962027 | ATCCAATTACTGGAA[A/G]TAAGTTATTCTATTC | 7874 |
rs756274054 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8922254 | AGCACTTTGGCAGGC[C/T]GAGACAGGCAGATCA | 7874 |
rs756274505 | in-del | -/T | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8949657 | AATCTTGTTCTTCAA[-/T]TTCCAGGCCCCTATC | 7874 |
rs756307163 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8955234 | TTTTACATATTAATC[C/T]GTTTGCATTTCATTT | 7874 |
rs756320326 | in-del | -/TAAAA | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892606 | TGACTAGTTAGAGGC[-/TAAAA]AAAAAAAAAAAAAAA | 7874 |
rs756337262 | snp | A/G | 3.30207e-05 | 0.00406316 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8900550 | AAATACTATGATGTC[A/G]CCATCCATTAGTTCA | 7874 |
rs756374484 | snp | C/T | 1.65252e-05 | 0.00287443 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8895699 | TAATAGTTCATCTTC[C/T]TGATGAACACCAATG | 7874 |
rs756397128 | in-del | -/A | 1.79887e-05 | 0.002999 | intron-variant | USP7 | GRCh38.p7 | 16:8902485 | TTGTGGAAATCCCTG[-/A]AAAAAAATATTAAGA | 7874 |
rs756482546 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8928522 | TTCACAACACACTTA[G/T]CCCCTGAAGAAGAGG | 7874 |
rs756503862 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8919811 | ACCGTCACCAAGCGG[G/T]ACCAGTGCTGGGGGA | 7874 |
rs756504079 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8909295 | TTCCTTCTGGCTGGA[A/T]ATCCACCTGCCCAGC | 7874 |
rs756523988 | snp | A/G | | | intron-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894194 | GGCATGCATCCCTGT[A/G]GCTCCCCAAGGGGTA | 7874 |
rs756542003 | snp | C/T | 0.00970851 | 0.0689927 | intron-variant | USP7 | GRCh38.p7 | 16:8923175 | TAAAATTGCACTAGG[C/T]TGATCAAATTTGGCT | 7874 |
rs756542211 | snp | A/C | 1.6713e-05 | 0.00289072 | intron-variant | USP7 | GRCh38.p7 | 16:8915235 | AAAGATCATGCCATT[A/C]GATACACACAACACT | 7874 |
rs756550597 | snp | A/G | 1.65488e-05 | 0.00287647 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8921250 | CTTTTCATCATCTCT[A/G]TAATTTATTATCTTC | 7874 |
rs756551818 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8902518 | AGATTAAAATAAAAA[C/G]ACGCTCATATTTTAG | 7874 |
rs756558792 | in-del | -/AC | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956789 | AACAAAAAAAAAAAA[-/AC]ACTGAATTTGCTTTA | 7874 |
rs756594540 | snp | G/T | 1.84391e-05 | 0.00303632 | intron-variant | USP7 | GRCh38.p7 | 16:8898679 | TAAATGACTTGTTTA[G/T]TTGCCTAAAAACAAA | 7874 |
rs756598413 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8949449 | GTGGAGAAGAAAAGC[A/G]AAGTAACACAACACA | 7874 |
rs756615535 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893128 | TTTTTCCTTTTTTTT[C/T]CATTTTTAACTTTTT | 7874 |
rs756636137 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8954865 | CTCAGGAGGCTGAGG[C/T]GGGAGAATGGTGTGA | 7874 |
rs756639146 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8927751 | TGAGGCAGAAGAATC[A/G]CAAAAACCCAGGAGG | 7874 |
rs756640977 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960613 | CTGACAGTTTCCAGC[G/T]GCTAGTTCGTTAGGA | 7874 |
rs756662094 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8903964 | TAGCTAGACAGCCAA[C/T]GGTGAGATGACCTCC | 7874 |
rs756698302 | snp | A/C | 1.71202e-05 | 0.00292572 | intron-variant | USP7 | GRCh38.p7 | 16:8908463 | TTCCTAAACATTGAA[A/C]AACAAATGCAAATGT | 7874 |
rs756704784 | snp | A/C | 9.91129e-05 | 0.00703894 | intron-variant | USP7 | GRCh38.p7 | 16:8898477 | TCAGATACCGTCACC[A/C]AAACCCCGAGCCTTC | 7874 |
rs756725151 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8958180 | CAATGCCCATCCCAC[C/T]GGCACAGTAGCAGGT | 7874 |
rs756727367 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8959318 | ATACCATGAATTTTT[A/G]CTTAATGACCTCTTT | 7874 |
rs756740088 | in-del | -/TCAG | 1.78857e-05 | 0.00299041 | intron-variant | USP7 | GRCh38.p7 | 16:8923432 | AAAAAAAACACATCA[-/TCAG]TCAGTCACAGAGCCT | 7874 |
rs756770513 | in-del | -/C | | | intron-variant, frameshift-variant | USP7 | GRCh38.p7 | 16:8894525 | GAAACCCACACCAGC[-/C]CCCCGGGGGGGGGAG | 7874 |
rs756796166 | snp | C/T | | | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891989 | CTTTCTTTAAAATTT[C/T]AGCTTGTCTCCCCAG | 7874 |
rs756799606 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8947702 | TAACAGTAGCTATAA[A/C]CCACCCACCAAAAGC | 7874 |
rs756806626 | snp | A/T | 1.75342e-05 | 0.00296087 | intron-variant | USP7 | GRCh38.p7 | 16:8920481 | AATATCCAGCTTGAA[A/T]AAGAACACACATTTT | 7874 |
rs756826814 | snp | C/T | 1.65449e-05 | 0.00287614 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8894612 | TTTATGTACTGGTGT[C/T]GGCCCATCATTACAA | 7874 |
rs756849721 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8919754 | TCCTCCCACCTCCAC[A/G]CCCATCTCCCTCTGT | 7874 |
rs756870249 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8896184 | TGAAATATCAGAAAC[-/A]AGAGACCGGAGGCAA | 7874 |
rs756889676 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957345 | ATCTAACTCTGTCAT[C/G]GTACATGGCAAGAAA | 7874 |
rs756897316 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8924671 | TCACTAACAACTGAG[C/T]TCTCAGCATCAGCCA | 7874 |
rs756898166 | snp | A/G | 1.65343e-05 | 0.00287521 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8920388 | AGCATCCGCCTGTAC[A/G]AAGACTTCAAAGGTA | 7874 |
rs756940270 | in-del | -/TAGT | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950202 | TCAACCACATGTGGC[-/TAGT]GGCTGCCACAGTGGA | 7874 |
rs756980520 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8898489 | ACCAAAACCCCGAGC[C/T]TTCTCTTTATGACCC | 7874 |
rs757038154 | snp | C/G | 0.000428527 | 0.0146315 | intron-variant | USP7 | GRCh38.p7 | 16:8899805 | AAAGTCCATGGCAGG[C/G]GGTAGCTGGTAAAAA | 7874 |
rs757047883 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8896428 | TTATTAAAACTAAAG[A/G]AAGTTTGGGAACCAA | 7874 |
rs757087341 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8907606 | CACGCCAGTAATCCC[A/C]GCACTTTGGGAGGCT | 7874 |
rs757088246 | snp | C/T | 1.64933e-05 | 0.00287165 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8903284 | ATGGTCTGAGAGAGG[C/T]TCTGAACAAACTCAG | 7874 |
rs757112853 | snp | A/C | 1.67629e-05 | 0.00289503 | intron-variant | USP7 | GRCh38.p7 | 16:8930250 | GAACCTGTTTTCTGA[A/C]AAGTTTCCGCCCACT | 7874 |
rs757176466 | snp | A/G | 1.64781e-05 | 0.00287033 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8910787 | TTTATTGTCCCCATC[A/G]AGCTGTTCTACTGCC | 7874 |
rs757187459 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8910937 | TAGCAGAGAAGGTAA[A/G]CAACACTAACAGTAA | 7874 |
rs757221160 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938333 | AGTCTTAAGAAATAA[C/T]ACAGTCAAAAAAAAA | 7874 |
rs757228897 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8939881 | AAGGAGGGCAGATCA[C/T]GAGGTCAGGAGATTG | 7874 |
rs757242368 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8892218 | TGTTCAAAGACAAAC[A/C]CACAGCGAACGGCTC | 7874 |
rs757242380 | snp | G/T | | | intron-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894261 | ACCTGGAGCTAAGGA[G/T]GCCCACACCCTGACT | 7874 |
rs757271539 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8928594 | CTACAAGTTCTTCTC[C/G]TACAGTCAGGACCAC | 7874 |
rs757295570 | snp | A/T | 1.65149e-05 | 0.00287353 | intron-variant | USP7 | GRCh38.p7 | 16:8902225 | TTTTAGAAGAGTCTA[A/T]TGGCTTAGGTGACAG | 7874 |
rs757311930 | snp | C/T | 3.29707e-05 | 0.00406008 | intron-variant | USP7 | GRCh38.p7 | 16:8905371 | GCAGCGATCAAGCAC[C/T]GTGACAAGTACCCAA | 7874 |
rs757320256 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8939268 | ACCCACCCCGGCGTG[C/T]GTGCTCCCCCATTAT | 7874 |
rs757323028 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8904188 | GTGTATCAGGAACTA[C/T]TCTGGGACTGTGACC | 7874 |
rs757335070 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8943671 | AGCATATGGGTAGAG[C/T]CGAATGGCTGGCGGG | 7874 |
rs757349492 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8927961 | ACCAGCCTGGGTAAC[A/G]TAGTGACATCCCATC | 7874 |
rs757358996 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938144 | GAATGGAAAAGTCCT[A/G]AGCAAACAGGCACGA | 7874 |
rs757370621 | snp | A/C/G | 0.000106533 | 0.00729775 | intron-variant | USP7 | GRCh38.p7 | 16:8906612 | TTTAAAAGAAATTCA[A/C/G]TATTAATTTACACAA | 7874 |
rs757406176 | snp | C/T | 1.65277e-05 | 0.00287464 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8899149 | AAAACTGCAGCAACA[C/T]TGGATCTGTGTTGAG | 7874 |
rs757430638 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960883 | ACCAGTGGGTACTCA[C/T]AGGGCACTATTATTT | 7874 |
rs757438716 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8936992 | GGCGCTCTGTCATAA[C/T]TTTGCAACTTTTCTG | 7874 |
rs757472416 | snp | A/G | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8897026 | GATGCTTTCTCCCCA[A/G]GCTCCACGGCCTTTT | 7874 |
rs757506773 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8934049 | AGGCGTGAAACACCA[C/T]GCCTGGCCTATAAAT | 7874 |
rs757525783 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8911131 | TTATGAAGACAGCTT[C/G]GAATTGGGCAGTGTG | 7874 |
rs757541461 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8914204 | AACAACCTCACTGAT[C/T]TTCAAGGAAATACAA | 7874 |
rs757555842 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8902625 | CCAGGTGCTGTGGCT[C/G]TCGCCTGTAATCCCA | 7874 |
rs757558884 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8945810 | AATCCCAGCACTTTA[G/T]GAAGCCAAGGCAAGA | 7874 |
rs757568278 | in-del | -/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8926651 | GGATCCTATGTATTA[-/T]TTTTTTTGCAACTTC | 7874 |
rs757672263 | snp | A/G | 1.64803e-05 | 0.00287052 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8904467 | GATGGGCTTCCTGCC[A/G]CTCCTTCCGCTTCTG | 7874 |
rs757686631 | snp | A/C | 1.6492e-05 | 0.00287154 | intron-variant | USP7 | GRCh38.p7 | 16:8895189 | AGTTCTGTAAGTGCA[A/C]GTGATGTGGTCAAAG | 7874 |
rs757705172 | snp | C/T | 0.000115303 | 0.00759199 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8895091 | CTCTTTGTGGAAATG[C/T]GCCACTGTGACAAGC | 7874 |
rs757720350 | in-del | -/AAGAG | 1.90547e-05 | 0.00308658 | intron-variant | USP7 | GRCh38.p7 | 16:8902497 | CCTGAAAAAAATATT[-/AAGAG]TAGATTAAAATAAAA | 7874 |
rs757761556 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8941550 | AGCCAAAACACATTT[C/T]GGCTTTTTTGTCCAC | 7874 |
rs757763150 | in-del | -/A | 5.73356e-05 | 0.00535393 | intron-variant | USP7 | GRCh38.p7 | 16:8898692 | TATTTGCCTAAAAAC[-/A]AATATCTGTGAGTGA | 7874 |
rs757781723 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8919937 | ACCCCTCTTTACTCC[C/T]CGCTCACCATGTTAG | 7874 |
rs757786416 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938224 | ATATTCCCAAAATAA[C/T]CTGGATTCCTGTAGG | 7874 |
rs757793107 | snp | C/T | 1.66029e-05 | 0.00288117 | intron-variant | USP7 | GRCh38.p7 | 16:8899553 | ATTTTAAGAAAGAAA[C/T]TTGTCTTTCTGGAGT | 7874 |
rs757808427 | snp | A/C | 0.0219753 | 0.102493 | intron-variant | USP7 | GRCh38.p7 | 16:8923180 | TTGCACTAGGCTGAT[A/C]AAATTTGGCTTCCAG | 7874 |
rs757817893 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8951476 | GGGCTCACCCACCTC[A/G]CCCTGAGCCAGCCGG | 7874 |
rs757836334 | snp | C/T | 3.29478e-05 | 0.00405867 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8894799 | CTTCTCAAACTCCTT[C/T]TCCTGGATGTCCAGC | 7874 |
rs757853177 | snp | A/C | | | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962152 | TGAGCTCCCCTGGAG[A/C]TTCATTCATTGAGGC | 7874 |
rs757854077 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8896508 | GAGAATCATGCCCAT[C/T]TCTCTGAAATAAACA | 7874 |
rs757865975 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8907804 | GGGCGACACAGCAAG[A/T]CTCTGTCTCAAAAAC | 7874 |
rs757907405 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950284 | GCTTGCAGAGTAGAA[A/G]ACACAACAGACATTT | 7874 |
rs757937059 | snp | A/G | 1.64762e-05 | 0.00287016 | intron-variant | USP7 | GRCh38.p7 | 16:8894733 | GCCGCTACGCTAGGC[A/G]AGGCTTGAGCCTATG | 7874 |
rs757948670 | snp | C/T | 3.29669e-05 | 0.00405984 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8903297 | GGCTCTGAACAAACT[C/T]AGCAAGCGAGGAGTT | 7874 |
rs757960520 | snp | A/G | 1.6865e-05 | 0.00290383 | intron-variant | USP7 | GRCh38.p7 | 16:8915210 | CATTAAAACACAGTA[A/G]AAATCATCAAAAGAT | 7874 |
rs757978692 | in-del | -/AACTC | | | intron-variant | USP7 | GRCh38.p7 | 16:8918334 | TCTCAAAATAGAACT[-/AACTC]ATCTATATTAGATTT | 7874 |
rs757999202 | snp | A/G | 1.65184e-05 | 0.00287384 | intron-variant | USP7 | GRCh38.p7 | 16:8898486 | GTCACCAAAACCCCG[A/G]GCCTTCTCTTTATGA | 7874 |
rs758002791 | snp | C/T | 1.79383e-05 | 0.0029948 | intron-variant | USP7 | GRCh38.p7 | 16:8920491 | TTGAATAAGAACACA[C/T]ATTTTATTCCCAAGA | 7874 |
rs758010381 | snp | C/T | 1.65644e-05 | 0.00287783 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8920424 | GTCATCATCTATAAA[C/T]CCTTTCTCAGGATCG | 7874 |
rs758062689 | in-del | -/A | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950285 | CTTGCAGAGTAGAAG[-/A]CACAACAGACATTTT | 7874 |
rs758068175 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8926390 | AGGTCGAGGCAGGAG[A/T]ATCGCTTGAACCTGG | 7874 |
rs758084904 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8958347 | ATGTGTGCTGGGAAC[C/T]GGCAGCACCAAGGAG | 7874 |
rs758094459 | snp | C/G | 0.000315706 | 0.01256 | utr-variant-5-prime, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8963321 | CGCCTGCGGCCGGGG[C/G]CCGGGGCTGCGAGCC | 7874 |
rs758168602 | snp | A/G | 3.2956e-05 | 0.00405918 | intron-variant | USP7 | GRCh38.p7 | 16:8919005 | GGTGAGCGGAAGGCT[A/G]CAGGAGAGGAACACT | 7874 |
rs758205794 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8922973 | CAATGGTCAGCTAAT[A/C]CAGGCCGGCCCTGAT | 7874 |
rs758213013 | snp | G/T | 1.65233e-05 | 0.00287426 | intron-variant | USP7 | GRCh38.p7 | 16:8896952 | GAGGTCAGCGTTAAC[G/T]GCCACCCCTAACTGA | 7874 |
rs758216906 | snp | A/G | 1.64879e-05 | 0.00287118 | intron-variant | USP7 | GRCh38.p7 | 16:8899809 | TCCATGGCAGGGGGT[A/G]GCTGGTAAAAATGGC | 7874 |
rs758220773 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8954792 | GGTAAAACCCCCCCT[C/G]TACTAAAGATACAAA | 7874 |
rs758229570 | snp | A/G | 1.64944e-05 | 0.00287175 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8900565 | ACCATCCATTAGTTC[A/G]TCAAGGGCTTTATCA | 7874 |
rs758239294 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8931944 | CAACTGCATACAGGA[A/G]ATGTGCTTTTTAACA | 7874 |
rs758246356 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8898899 | GGGAGATGCACTGAG[G/T]ATGTATCTAAAGTCA | 7874 |
rs758258486 | snp | G/T | 1.65045e-05 | 0.00287263 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8917147 | CCTCGGTTGGCATCA[G/T]GTACACAGCCTGAAA | 7874 |
rs758258556 | snp | A/G | 5.20332e-05 | 0.00510038 | intron-variant | USP7 | GRCh38.p7 | 16:8930404 | TATCTCCCGCTTTAA[A/G]GAAGAAAAAGAAATT | 7874 |
rs758274961 | snp | A/G/T | 8.25204e-05 | 0.00642294 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8930315 | CATGTCCTCCTCCGC[A/G/T]GTGTTGTGTCCATCA | 7874 |
rs758373534 | snp | A/G | 1.66854e-05 | 0.00288833 | intron-variant | USP7 | GRCh38.p7 | 16:8903413 | ACTATCTGAAAATAT[A/G]TATGAAAGCACAGAA | 7874 |
rs758386659 | in-del | -/AG | | | intron-variant | USP7 | GRCh38.p7 | 16:8934617 | AAACGCAAAGCAAGC[-/AG]AGGTCTGCGGTTGCA | 7874 |
rs758408144 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8920635 | TCACAACAAATACAG[C/T]AAATGCTTGGCACCT | 7874 |
rs758414236 | in-del | -/TCC | 1.65192e-05 | 0.00287391 | cds-indel, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8930304 | TTACCATCCTCCATG[-/TCC]TCCTCCGCGGTGTTG | 7874 |
rs758419501 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8951776 | CAGCATGGTTTGCTT[C/T]AGGAATGATTCATTC | 7874 |
rs758420268 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8931136 | TACTGAACATATGCA[A/C]ATGGTATACATTAAA | 7874 |
rs758448369 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8926945 | CTACAGCACGAAGTT[C/G]CCACTGTGCACTTTG | 7874 |
rs758496087 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8919958 | ACCATGTTAGTTGTC[A/G]GTGATGCTCACCTCT | 7874 |
rs758498206 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8929347 | GGTAACAAAGCAGCG[C/G]GTTTAGACCACGCCT | 7874 |
rs758501837 | snp | A/G | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8899662 | GGATCATTAGGGATT[A/G]TTTTATCACAGAAAA | 7874 |
rs758505608 | snp | C/T | | | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962231 | TTCATTCAGGTGGCC[C/T]CCATTTGACTCCCGA | 7874 |
rs758515943 | snp | A/G | | | intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962983 | GCCCGGCGGACGCGA[A/G]GTCGGGACAATGCAC | 7874 |
rs758523367 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8896039 | ACGGGGTTTCACCAT[A/G]TTGGTTAGCCAGGAT | 7874 |
rs758550046 | snp | A/G | 1.64819e-05 | 0.00287066 | intron-variant | USP7 | GRCh38.p7 | 16:8895153 | CCAAAGGGATTTCCT[A/G]GGGACACGGACAACA | 7874 |
rs758589839 | snp | A/G | 1.64868e-05 | 0.00287109 | missense, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8923369 | TCAGTCTGCTGAAGC[A/G]CTCCACAGTGAACTG | 7874 |
rs758591289 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8928700 | AGGAAAGGTGCTACG[A/G]AAGATTACTCAACCT | 7874 |
rs758597027 | snp | A/G | 1.65397e-05 | 0.00287569 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8894584 | TTTCAAATTTACTTC[A/G]TACTCGTCTTCATTT | 7874 |
rs758633494 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8925327 | GAGACTACTAGCTTG[C/T]CCGCTTTATGAAGCC | 7874 |
rs758661660 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8907269 | ATAAAAACAAAGTGA[A/G]GATCCAAAGAAACAT | 7874 |
rs758678536 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8900823 | GATTCTACAACAGGT[-/A]AAAAAAAAAAATTCA | 7874 |
rs758682269 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957279 | TCCTCCAACTTTCTT[A/C]AGTCCAAATTAGTTC | 7874 |
rs758731615 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8911911 | GGGAAGTCTGTGTTC[C/T]CACCAGCCACCGTGG | 7874 |
rs758748076 | snp | A/G | 1.64789e-05 | 0.0028704 | intron-variant | USP7 | GRCh38.p7 | 16:8905172 | AAGAACAGAACAAAA[A/G]TGAACACTACTCACT | 7874 |
rs758764377 | snp | A/G | 0.0425331 | 0.13949 | intron-variant | USP7 | GRCh38.p7 | 16:8916590 | ACAACTCCATTTAAA[A/G]CTCAACTTTCAAATG | 7874 |
rs758777326 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957460 | GCAAAAAACCATAAA[C/T]GGGCTGGGTGAGGTG | 7874 |
rs758781731 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8935491 | GCTGGGATTACAGGC[A/G]TGGGCCACCATGCCC | 7874 |
rs758810531 | in-del | -/G | 1.66955e-05 | 0.0028892 | intron-variant | USP7 | GRCh38.p7 | 16:8903240 | GTTGGGAGCCACGGT[-/G]GGGTATATCCACGGG | 7874 |
rs758828660 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8939884 | GAGGGCAGATCACGA[A/G]GTCAGGAGATTGAAA | 7874 |
rs758845701 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8901757 | GCCTGAAACGCCTGA[A/G]ATATTGCCTATGTGG | 7874 |
rs758865895 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8934627 | CAAGCAGAGGTCTGC[A/G]GTTGCAGCAGAATCT | 7874 |
rs758874521 | snp | A/T | 3.31115e-05 | 0.00406874 | intron-variant | USP7 | GRCh38.p7 | 16:8904582 | TGCAGGACAAAGGCA[A/T]CCTCTTTGACCCCTG | 7874 |
rs758915094 | in-del | -/AAAAAAA | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892607 | GACTAGTTAGAGGCT[-/AAAAAAA]AAAAAAAAAAAAAAA | 7874 |
rs758917003 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8926286 | AGTTTGAGACCAGCC[G/T]GCCCAACATGGTGAA | 7874 |
rs758920675 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8910128 | CAATGAGTCAAGGTT[A/G]TAAGATTACAAAACA | 7874 |
rs758973927 | in-del | -/CA | | | intron-variant | USP7 | GRCh38.p7 | 16:8941937 | AATAGAGGGCAAACG[-/CA]CACAGTGACAGCCAC | 7874 |
rs758993686 | snp | A/C | 0.000371609 | 0.0136259 | intron-variant, utr-variant-5-prime | USP7 | GRCh38.p7 | 16:8929541 | AACTGCCCCGTTACT[A/C]CCCTGGGAAGGACAC | 7874 |
rs758999125 | snp | C/T | 4.99563e-05 | 0.00499756 | intron-variant | USP7 | GRCh38.p7 | 16:8899228 | CATTTTGGGGAAAAA[C/T]TGAAACTTGGTCATA | 7874 |
rs759010809 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8952888 | GTCGCCCAGGCTAGA[A/G]TGCACTGGCGCAATC | 7874 |
rs759031766 | snp | C/G | | | intron-variant, missense | USP7 | GRCh38.p7 | 16:8894435 | TGGTTCCACAGGTCG[C/G]CCAGTGGAGAGAGAG | 7874 |
rs759038458 | in-del | -/AG | 0.42 | 0.183303 | intron-variant | USP7 | GRCh38.p7 | 16:8910833 | ATTCAAATACTTTAA[-/AG]AGAGAGAGAGAGAAA | 7874 |
rs759063150 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8920231 | GTGTGACTCTGTGTG[C/T]CACAGGGCAAGCGCA | 7874 |
rs759086930 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961352 | ACAAAAGTAGCCAGG[C/T]GTGGTTGCACATGGC | 7874 |
rs759095315 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8938831 | ATTTACACTGTATTA[C/G]ATATTATAAGCCACG | 7874 |
rs759100414 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8923313 | CATAATCTTCCATGG[C/T]AGATTTCGCACAAAA | 7874 |
rs759118293 | in-del | -/ATTAAGAGTAG | 0.00108653 | 0.0232827 | intron-variant | USP7 | GRCh38.p7 | 16:8902494 | ATCCCTGAAAAAAAT[-/ATTAAGAGTAG]ATTAAAATAAAAACA | 7874 |
rs759118863 | snp | A/G | 3.5312e-05 | 0.00420175 | intron-variant | USP7 | GRCh38.p7 | 16:8921340 | TGACATTATTTACCA[A/G]ATGTTATACATTTTT | 7874 |
rs759156719 | snp | C/G | 1.711e-05 | 0.00292484 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8902382 | TTAACAATATTTACT[C/G]TTTTATTGCCGTCGG | 7874 |
rs759156854 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8929081 | AGTAGGGAAATGTTG[C/G]AACAGATTGCTCTGT | 7874 |
rs759181223 | snp | C/G | 0.000300298 | 0.0122498 | intron-variant, synonymous-codon | USP7 | GRCh38.p7 | 16:8894536 | CCAGCCCCCGGGGGG[C/G]GGAGAACCCTTACCG | 7874 |
rs759212008 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957799 | TTAAAAACACAAAAA[C/T]GATAACAAAAATAGA | 7874 |
rs759214490 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8905021 | TACTTGGTACCATAA[G/T]TCTGCATCGAAACGC | 7874 |
rs759232846 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8902023 | GTGTGTTTAGAACAA[C/G]AATCCAGGAATCCAA | 7874 |
rs759247325 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8928353 | CAAAAAAAGGGGGAG[A/C]TCTGAAGTCCAGAGT | 7874 |
rs759250430 | in-del | -/GATGGGGCTCAT | 1.65231e-05 | 0.00287424 | intron-variant | USP7 | GRCh38.p7 | 16:8895592 | TTTAAATATGCAGCA[-/GATGGGGCTCAT]GAATTCTCTCTGGTG | 7874 |
rs759258864 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893890 | AATTAACACCAGCAG[C/T]GAATCCTCTTGCTGA | 7874 |
rs759285520 | in-del | -/A | 0.000118838 | 0.00770747 | intron-variant | USP7 | GRCh38.p7 | 16:8915548 | GAATGTTTTGGCTTT[-/A]AAAAAAACTTTTTTG | 7874 |
rs759299374 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960349 | CCTAACTGCTCAGGG[C/G]ATTTCAAAAAATAAC | 7874 |
rs759302498 | snp | A/G | 1.6661e-05 | 0.00288621 | intron-variant | USP7 | GRCh38.p7 | 16:8920341 | TTTTTAACAGCACCT[A/G]ATTAAAGAAAAACTT | 7874 |
rs759303965 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8911718 | AGCGGGAACCTGCTG[A/G]GCAGAGTAGCCTAAA | 7874 |
rs759312352 | snp | A/T | 7.21683e-05 | 0.00600657 | utr-variant-5-prime, intron-variant | USP7 | GRCh38.p7 | 16:8936648 | GGCCTCTGCTGGGGG[A/T]TGGGGGAGGTTCTCT | 7874 |
rs759338872 | snp | C/T | 1.64982e-05 | 0.00287208 | intron-variant | USP7 | GRCh38.p7 | 16:8916485 | TAAGAAATATACAAG[C/T]ATTGCTTGAAACTTA | 7874 |
rs759348816 | snp | C/G | 0.000202984 | 0.0100723 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962487 | TTACCTTTCGAGTCA[C/G]GTTTGATTCTGATGC | 7874 |
rs759446509 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8901407 | TTCAGATGTGGCTTA[G/T]TCACGAAGCTGAGGC | 7874 |
rs759461883 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8933514 | TCAAAAGATGTCTAC[A/C]GAAACAGCAGGATAC | 7874 |
rs759468411 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8943355 | ATGTATAGTCTGCTC[C/T]GCAAAAGAAACAGGA | 7874 |
rs759508713 | snp | A/G | 3.31532e-05 | 0.0040713 | missense, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8930380 | GAGTAATTCTTGGTG[A/G]GTCATCTGTATCTCC | 7874 |
rs759520213 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8910961 | ACAGTAACTCTCCCC[C/T]TGTAGCCAAGACTGT | 7874 |
rs759535435 | snp | C/G | 8.24463e-05 | 0.00642 | intron-variant | USP7 | GRCh38.p7 | 16:8895180 | AACAGACACAGTTCT[C/G]TAAGTGCAAGTGATG | 7874 |
rs759598815 | snp | C/T | 5.01819e-05 | 0.00500884 | intron-variant | USP7 | GRCh38.p7 | 16:8904400 | GGGTGCCCGGCTGCA[C/T]GGTGACCCGGAGTCC | 7874 |
rs759611555 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8919386 | GGCACTCCTGTCACT[C/G]ATCAAGCCCAGCACC | 7874 |
rs759618317 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8951552 | CCTATTTGCTCATCT[A/G]TAAATGCAGAGGGCT | 7874 |
rs759678122 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8907444 | CTGAAGGCTGAATGA[C/T]CAACCTATATTCCAT | 7874 |
rs759710157 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8931573 | AGGAAAGGATAAAAT[G/T]GTTTTACCACTCTAA | 7874 |
rs759726151 | snp | A/C | 1.65638e-05 | 0.00287778 | intron-variant | USP7 | GRCh38.p7 | 16:8930283 | GAGGCGGTGAACCAC[A/C]GGCACTTACCATCCT | 7874 |
rs759732382 | snp | A/G | 1.64912e-05 | 0.00287147 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8908376 | TTGGTCCGTCTGAGG[A/G]TCATACATAAATCTC | 7874 |
rs759752579 | snp | A/T | 1.67518e-05 | 0.00289407 | intron-variant | USP7 | GRCh38.p7 | 16:8910871 | TGCTAAAGCTTCATT[A/T]ATAATGTAGCCAACA | 7874 |
rs759805104 | snp | A/G | 4.94246e-05 | 0.0049709 | intron-variant | USP7 | GRCh38.p7 | 16:8894875 | AATGGCAAAGGACAT[A/G]TGCTCACACAGTCAC | 7874 |
rs759815784 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8912232 | AGAGGTACGTGGATC[A/G]CCTGAGGTCAGGAGT | 7874 |
rs759868690 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8903758 | TGTAATCCCAGCTAC[G/T]AGGAAGGCTGAGGCA | 7874 |
rs759868748 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8915035 | GGTTTCCTGTGAGGA[A/G]AGGGGAGGTGGTGGC | 7874 |
rs759875521 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937651 | GCACCACTGCCATTC[C/T]AGCCTGGGCAACAAA | 7874 |
rs759900645 | snp | C/T | 1.64765e-05 | 0.00287019 | intron-variant | USP7 | GRCh38.p7 | 16:8894760 | TATGGCCCGCCAAGC[C/T]CCCAGGAGGCCCCAG | 7874 |
rs759903106 | in-del | -/TGG | 0.000198886 | 0.00997013 | cds-indel, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8963274 | TGCTGCTGCTGCTGC[-/TGG]TGGTGGTTCATGTCG | 7874 |
rs759933694 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8945513 | ACCAACAGACACCTT[C/G]AACATTTCTGTGCAC | 7874 |
rs759938727 | snp | A/G | 1.65026e-05 | 0.00287246 | intron-variant | USP7 | GRCh38.p7 | 16:8902205 | ATTTCCAAAAGAGAC[A/G]CTGATTTTAGAAGAG | 7874 |
rs759965148 | snp | C/T | 1.65034e-05 | 0.00287253 | intron-variant | USP7 | GRCh38.p7 | 16:8896978 | ACTGAACGTCCACAA[C/T]TGGGCTCAAGAAATA | 7874 |
rs759969636 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8946362 | GAGGCAGGAGGATCA[C/T]TTGTGGCCAGGAGTT | 7874 |
rs759972735 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8922653 | GACAGGTTGACAAAG[C/T]GGTCCGTACTCCCAG | 7874 |
rs759988536 | snp | A/G | 1.67217e-05 | 0.00289147 | intron-variant | USP7 | GRCh38.p7 | 16:8906392 | TGTTAACTTTCTGAT[A/G]AGCTTGCATTCAGCC | 7874 |
rs760007496 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8915962 | CAAAAAAGAAAACAC[-/A]CCTTGCCCAGCCAAT | 7874 |
rs760071279 | snp | C/T | 1.6869e-05 | 0.00290417 | intron-variant | USP7 | GRCh38.p7 | 16:8900651 | GTGAAAGATATAAAA[C/T]TGTTACACTGCAAGT | 7874 |
rs760071509 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8943050 | CAAAGTGGACCCACT[C/T]TGACGCTTTGCTCTA | 7874 |
rs760084400 | snp | A/C | 1.64827e-05 | 0.00287073 | intron-variant | USP7 | GRCh38.p7 | 16:8918988 | TATACCTGAGAAGAA[A/C]GGGTGAGCGGAAGGC | 7874 |
rs760090222 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8924366 | ACACAAGCTTCTAAA[C/T]GCTTCCTTTCACTTT | 7874 |
rs760109853 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8934471 | TTACAGGATGGGGTG[C/G]GGGAAATGCGTAAGC | 7874 |
rs760213980 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8952458 | CCAAGGTGCCAGCAG[A/G]GCCACATTCCTTCTG | 7874 |
rs760219093 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8911805 | CAGTGAGAACTGATC[A/G]GTGAACTCGAGGAAA | 7874 |
rs760224918 | snp | C/T | 1.64906e-05 | 0.00287142 | intron-variant | USP7 | GRCh38.p7 | 16:8905137 | GATTCATGGTACAAA[C/T]GTCCAAGTCCACCAC | 7874 |
rs760277545 | snp | A/G | 1.65919e-05 | 0.00288022 | intron-variant | USP7 | GRCh38.p7 | 16:8915536 | AGCAACTGAAAAAGA[A/G]TGTTTTGGCTTTAAA | 7874 |
rs760295224 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8899723 | AATACTCCTTTGCGG[C/T]GGGTAATTCACTGTT | 7874 |
rs760296831 | in-del | -/AAAA | 2.31747e-05 | 0.00340394 | intron-variant | USP7 | GRCh38.p7 | 16:8895755 | GCCTGAACAGAGAGG[-/AAAA]AAAAATAGGGCAAAA | 7874 |
rs760306013 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957906 | TACTTCCAAAAGGAT[A/C]AAAAAAACACCATTA | 7874 |
rs760351606 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8909208 | ATCAGGCTTTGCCTA[C/T]CTCGACCACGGCCAG | 7874 |
rs760352754 | snp | A/T | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8910757 | TACCTGTAAGCCATG[A/T]TCCCCAGCGTCGTAT | 7874 |
rs760361068 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892439 | CCGTGCCACGGAGCT[A/G]GAAGGCAAGGCCGAT | 7874 |
rs760392428 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8939541 | TTGAGTTCTGAAAGA[A/G]GTAAACACAAGCAAG | 7874 |
rs760398818 | in-del | -/CT | 5.20847e-05 | 0.0051029 | intron-variant | USP7 | GRCh38.p7 | 16:8915556 | TTGGCTTTAAAAAAA[-/CT]TTTTTGTACTTAGTA | 7874 |
rs760418018 | snp | A/G | 1.73051e-05 | 0.00294147 | intron-variant | USP7 | GRCh38.p7 | 16:8901285 | AACACTCAGCACAAT[A/G]CTTAAAAAACAAAAA | 7874 |
rs760442003 | snp | A/T | 1.65138e-05 | 0.00287343 | intron-variant | USP7 | GRCh38.p7 | 16:8899591 | GAAGAGGAAAGGAGC[A/T]TTTATTAAATACCTG | 7874 |
rs760449017 | snp | C/G | 0.000156859 | 0.00885464 | intron-variant | USP7 | GRCh38.p7 | 16:8920475 | AATAAGAATATCCAG[C/G]TTGAATAAGAACACA | 7874 |
rs760482616 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8919622 | TTTATTTTGTGATTT[G/T]GGTGGTTGTTTGGGA | 7874 |
rs760490498 | snp | C/T | 1.65619e-05 | 0.00287762 | intron-variant | USP7 | GRCh38.p7 | 16:8921125 | CAAGCAGTAATGCAC[C/T]AATTGTTCAGACTAA | 7874 |
rs760520122 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961875 | GGGCCAAGTGAAACA[C/G]ATAACCCAGTCCTTG | 7874 |
rs760574968 | snp | C/T | 1.65244e-05 | 0.00287436 | intron-variant | USP7 | GRCh38.p7 | 16:8898467 | AAGATTCACATCAGA[C/T]ACCGTCACCAAAACC | 7874 |
rs760592224 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8925182 | CCGAGGCTGTTTTAC[A/C]AAGTGACAATAGAGG | 7874 |
rs760616178 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956717 | GCAGTGAGCCGAGAT[C/T]GTCCCACTGCACTCC | 7874 |
rs760625920 | snp | C/G | 0.000206292 | 0.010154 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962513 | GATGCAGGCAGCCAT[C/G]TGCGGCAGGGCTTTC | 7874 |
rs760642091 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8958066 | ACACTGAAAAAAGTG[C/T]TTCCTGAATGAGCAT | 7874 |
rs760642910 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8919113 | TTCTTTAAGCCGACG[C/T]AGCCTGTGTGCTTCT | 7874 |
rs760655101 | in-del | -/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8911582 | GTACAGGACAGGGAT[-/C]CCTGAAGGGACAAAT | 7874 |
rs760661247 | snp | C/G | 1.65293e-05 | 0.00287479 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8901016 | TAAGGCTAGTATCTT[C/G]AATAAATCCTGCTCT | 7874 |
rs760698171 | snp | A/C/G/T | 0.000132036 | 0.00812416 | intron-variant | USP7 | GRCh38.p7 | 16:8902208 | TCCAAAAGAGACGCT[A/C/G/T]ATTTTAGAAGAGTCT | 7874 |
rs760711890 | snp | A/G | 3.29576e-05 | 0.00405928 | intron-variant | USP7 | GRCh38.p7 | 16:8901131 | AGAAGGTAAGTGCAC[A/G]AAGGACTTACGTATT | 7874 |
rs760748769 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8898208 | CCTGCCAGGAGGCAG[A/G]AAAGACTGGCCCAGG | 7874 |
rs760771572 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8914105 | AAAAAGAAAAGAAGC[C/G]AATACTAAAATTGTT | 7874 |
rs760797849 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8923899 | CTGGAAGCTCAGCAC[C/T]GCTCAGAGGCAAGAC | 7874 |
rs760803003 | snp | A/C | 0.000138956 | 0.0083342 | intron-variant | USP7 | GRCh38.p7 | 16:8936547 | TATCTCCATCCATCA[A/C]CAGCATAAGGAGCTC | 7874 |
rs760819636 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8898844 | CTGCAATAGTGACAA[A/G]ACACACAGCAGCCTG | 7874 |
rs760869749 | snp | A/G | 3.2963e-05 | 0.00405961 | intron-variant | USP7 | GRCh38.p7 | 16:8918995 | GAGAAGAAAGGGTGA[A/G]CGGAAGGCTGCAGGA | 7874 |
rs760874041 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8899944 | GGCAAGTATGCATGG[A/G]GATGCACTGAGCCAG | 7874 |
rs760888398 | snp | C/T | 1.69963e-05 | 0.00291511 | splice-acceptor-variant | USP7 | GRCh38.p7 | 16:8930398 | CATCTGTATCTCCCG[C/T]TTTAAAGAAGAAAAA | 7874 |
rs760889556 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8933243 | GCACCCAGCTCCCAA[C/T]AGAATGTTAAAAAAA | 7874 |
rs760893075 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8909623 | TCTTCATCACACCAA[C/G]TTCTCATTAAAAAGC | 7874 |
rs760894362 | in-del | -/T | 1.67506e-05 | 0.00289396 | intron-variant | USP7 | GRCh38.p7 | 16:8906379 | GAAGCAGAGCTTGTG[-/T]TAACTTTCTGATGAG | 7874 |
rs761005610 | snp | A/C | 0.000117027 | 0.0076485 | intron-variant | USP7 | GRCh38.p7 | 16:8904407 | CGGCTGCATGGTGAC[A/C]CGGAGTCCCAGAAGG | 7874 |
rs761007449 | snp | G/T | 3.29468e-05 | 0.00405861 | missense, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8923336 | GCACAAAACACGGAG[G/T]GCTAAGGACCGACTC | 7874 |
rs761026371 | snp | A/G | 1.64732e-05 | 0.0028699 | intron-variant | USP7 | GRCh38.p7 | 16:8895015 | GTGAGCCACTCGGCC[A/G]ACCACAACAGCATAC | 7874 |
rs761056216 | snp | A/G | 1.66918e-05 | 0.00288888 | intron-variant, missense | USP7 | GRCh38.p7 | 16:8894540 | CCCCCGGGGGGGGGA[A/G]AACCCTTACCGGGCT | 7874 |
rs761059024 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8929119 | AGACCCGGAATGTTC[C/T]GATAGGGCAGGGCCT | 7874 |
rs761076838 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8938916 | CACTGTTTTGTATGA[C/G]GAAGACTTGAGCATC | 7874 |
rs761081264 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8905891 | ACACGCACTCTTCAC[C/T]GTTCTCTCGTGCTGT | 7874 |
rs761081792 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937992 | TGAGCCCCTATTATG[A/T]GCCAGGCCTTGTACA | 7874 |
rs761104262 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8915191 | ATCACTTGTGTAAAT[A/G]AAACATTAAAACACA | 7874 |
rs761105770 | snp | C/G/T | 3.30492e-05 | 0.00406494 | intron-variant | USP7 | GRCh38.p7 | 16:8908327 | TCTTAACTTTATATC[C/G/T]CACTATAGATTACCT | 7874 |
rs761106835 | snp | A/C | 4.11091e-05 | 0.00453353 | intron-variant | USP7 | GRCh38.p7 | 16:8902511 | TAAGAGTAGATTAAA[A/C]TAAAAACACGCTCAT | 7874 |
rs761125187 | snp | C/T | 3.35993e-05 | 0.0040986 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8902395 | CTGTTTTATTGCCGT[C/T]GGCTTCATTATCTAA | 7874 |
rs761125465 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961663 | GTCATGGGAAATCCA[C/T]ATGCTCGTGTTATTG | 7874 |
rs761166778 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8946996 | GTAATGGGGCGGGGT[A/G]AATTAACCTTCATTA | 7874 |
rs761195918 | snp | A/G | 0.000234298 | 0.010821 | intron-variant | USP7 | GRCh38.p7 | 16:8920322 | CACTGCAGCACAAAA[A/G]ACATTTTTAACAGCA | 7874 |
rs761215552 | snp | A/G | 1.65116e-05 | 0.00287324 | intron-variant | USP7 | GRCh38.p7 | 16:8897115 | CTAAGTAATGAAAAG[A/G]TAAAATAAGTGCTTT | 7874 |
rs761215752 | snp | C/G/T | 0.000175273 | 0.00936011 | intron-variant, missense | USP7 | GRCh38.p7 | 16:8894526 | GAAACCCACACCAGC[C/G/T]CCCGGGGGGGGGAGA | 7874 |
rs761251731 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8935412 | GATGGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 7874 |
rs761254104 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8946665 | CATGGCAAAGGCACA[A/C]CTCCAATAATCTGGT | 7874 |
rs761254339 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8926552 | AGCTTTCACAGATAC[A/G]GCCAGCCAGATTGTC | 7874 |
rs761257708 | snp | C/T | 1.64819e-05 | 0.00287066 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893960 | TGTTAAGGGGCCACC[C/T]ACACACCGTCCTCGC | 7874 |
rs761296590 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8912805 | AAAAAAAAGAAGAGA[G/T]AAAGATTTTCATTTA | 7874 |
rs761300629 | snp | C/T | 0.000176227 | 0.00938522 | intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8963194 | CCCGCCGCGGCCGGC[C/T]CTCGGGCCTCACCTT | 7874 |
rs761303914 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961551 | GGACCTGGTCATTTT[C/T]CCAAAGATACAGGTC | 7874 |
rs761309921 | snp | A/T | 1.65269e-05 | 0.00287457 | intron-variant | USP7 | GRCh38.p7 | 16:8902038 | CAATCCAGGAATCCA[A/T]CGCTACTGCTCTAAG | 7874 |
rs761326339 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8905256 | CAGACAGGTCGTCAT[C/T]GTGACCCCCATAATT | 7874 |
rs761331464 | snp | C/T | 1.6916e-05 | 0.00290822 | intron-variant | USP7 | GRCh38.p7 | 16:8917014 | TGGCAAAGGCAGATG[C/T]CTAATACATACCCAA | 7874 |
rs761386549 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8921979 | AAGGGTAGGACAGTG[C/T]TGTTCCCACAGCACT | 7874 |
rs761428604 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8945314 | GTTTGTACCTGGGAG[C/G]TGGAGGTTGCAGTGA | 7874 |
rs761541410 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8911864 | AGAGGATGAGGATTG[A/G]GGGGAACAACCTTCA | 7874 |
rs761548193 | snp | A/T | 1.65048e-05 | 0.00287265 | intron-variant | USP7 | GRCh38.p7 | 16:8899088 | GGAAAGCATGCAGTC[A/T]AGACCAAGCAAGTGT | 7874 |
rs761548832 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8919500 | GCAAGGTCAGCACAA[A/C]GTGGAAAAAGCTGAA | 7874 |
rs761550770 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8908635 | GTTTATGGGTCTCTT[A/T]GTTTATTAAAATAAT | 7874 |
rs761601357 | snp | G/T | 4.94719e-05 | 0.00497328 | intron-variant | USP7 | GRCh38.p7 | 16:8895633 | GCCAACAGTATCGGG[G/T]ACAGATACCTCTATT | 7874 |
rs761640834 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8918744 | AACCCAGGAGACAGA[A/G]GCTGCAGTGAGCCAA | 7874 |
rs761654448 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8952150 | AGTCACTAGGGAGGC[C/T]GAGGTGGGAGGACTC | 7874 |
rs761687495 | in-del | -/CACTA | | | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964835 | AAAATAAAACAAGCC[-/CACTA]CCCTTCACATTTGGT | 7874 |
rs761690681 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8940473 | GGCGCCACCATCAAG[A/G]CTGTTGATCAGAGTG | 7874 |
rs761692904 | in-del | -/TC | 3.30699e-05 | 0.00406618 | intron-variant | USP7 | GRCh38.p7 | 16:8897130 | ATAAAATAAGTGCTT[-/TC]AAGAAAGCATAAAAG | 7874 |
rs761695762 | snp | A/G | 1.64844e-05 | 0.00287087 | intron-variant | USP7 | GRCh38.p7 | 16:8915351 | GATATAGGACTGCAA[A/G]TAAGGAAAGTAAAAG | 7874 |
rs761714224 | snp | A/T | 3.43932e-05 | 0.00414674 | intron-variant | USP7 | GRCh38.p7 | 16:8921322 | AATAATCTGAGCCTT[A/T]GTTGACATTATTTAC | 7874 |
rs761714457 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8959831 | CCCGTAACAAAAAAC[A/G]CAGAAGCCTAGATCA | 7874 |
rs761738032 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8948172 | CCTTTCCCACAGTTC[C/G]GCTCCCCTGATGGAA | 7874 |
rs761741958 | snp | A/T | 3.30573e-05 | 0.00406541 | intron-variant | USP7 | GRCh38.p7 | 16:8898453 | CTATTAAGAAAAGAA[A/T]GATTCACATCAGATA | 7874 |
rs761777331 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893398 | TGCAAAGGGGCTGCA[A/G]ACAGTAGTGGCTGAC | 7874 |
rs761788371 | snp | A/G | 6.59044e-05 | 0.00574002 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8902170 | CCAAGGGTTTTCATT[A/G]TCACTGAGCTCAATC | 7874 |
rs761792825 | in-del | -/T | 3.30096e-05 | 0.00406247 | intron-variant | USP7 | GRCh38.p7 | 16:8901073 | CTAGGAGAAAGAAGA[-/T]ATTTTAAATGTGTAG | 7874 |
rs761803936 | snp | A/C | 1.65263e-05 | 0.00287452 | intron-variant | USP7 | GRCh38.p7 | 16:8921144 | TGTTCAGACTAAATA[A/C]ACTGTTACTTACACT | 7874 |
rs761823844 | in-del | -/T | 3.31854e-05 | 0.00407328 | intron-variant | USP7 | GRCh38.p7 | 16:8908313 | CATGATGATGAAATC[-/T]TTAACTTTATATCCC | 7874 |
rs761824923 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8938947 | TGTGGATTTTGACAC[C/T]CTGAGAGGGGTCCTG | 7874 |
rs761862171 | snp | A/T | 5.13097e-05 | 0.0050648 | splice-acceptor-variant | USP7 | GRCh38.p7 | 16:8898641 | GGCCATCCCTATAAC[A/T]ACACAAGAAAACAGC | 7874 |
rs761903176 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8917659 | GCTGGGATTATAGGC[A/G]AGAGCTACCGCACCC | 7874 |
rs761937470 | snp | C/G | 1.67038e-05 | 0.00288992 | intron-variant | USP7 | GRCh38.p7 | 16:8920335 | AAGACATTTTTAACA[C/G]CACCTGATTAAAGAA | 7874 |
rs761982662 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8947202 | ATTACAACAGACAAT[A/G]AAGAAATTTACAAAA | 7874 |
rs761984134 | snp | A/G | 6.59283e-05 | 0.00574106 | intron-variant | USP7 | GRCh38.p7 | 16:8919147 | AATCCCACCTGAAAG[A/G]TCAGTTCAAGGTTGA | 7874 |
rs761985028 | snp | C/G | 1.65957e-05 | 0.00288055 | intron-variant | USP7 | GRCh38.p7 | 16:8897149 | GAAAGCATAAAAGGT[C/G]TGCTACCACAAAGGA | 7874 |
rs762005830 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8956165 | CTTAGTTACTGGCAT[A/G]TAATCAAAAAAGAGG | 7874 |
rs762026726 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8924929 | GCGCATCTTGTCCAA[A/G]ATAATTATTTATTTG | 7874 |
rs762074591 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893417 | GTAGTGGCTGACGAG[G/T]TGAGACAAGTTTATT | 7874 |
rs762086319 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8934335 | AATCAGACTGAGACA[A/C]AAGTGAATTCAGATT | 7874 |
rs762116730 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8924292 | CACCCACACCAATCT[A/G]TTATTGACCAATACT | 7874 |
rs762143956 | snp | C/G | 1.65184e-05 | 0.00287384 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8901027 | TCTTGAATAAATCCT[C/G]CTCTGTCACACATAA | 7874 |
rs762206887 | snp | A/G | 1.64803e-05 | 0.00287052 | intron-variant | USP7 | GRCh38.p7 | 16:8916565 | TTCCCACCTTTCAAA[A/G]ATAAAACAAACAACT | 7874 |
rs762232440 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8906019 | GCCCTCTACACTCCC[A/G]AGAGTGGTGGTGAAG | 7874 |
rs762239787 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964960 | TCCTGTCTCATTCAG[G/T]CATTGACAGACTGAT | 7874 |
rs762259530 | snp | A/G | 1.64754e-05 | 0.00287009 | intron-variant | USP7 | GRCh38.p7 | 16:8899766 | GTCATCCCTGGTGGA[A/G]GGAGAAAGTTTGCAG | 7874 |
rs762298878 | snp | A/G | 9.16128e-05 | 0.00676742 | intron-variant | USP7 | GRCh38.p7 | 16:8923444 | ATCATCAGTCACAGA[A/G]CCTGTGCATTGACCA | 7874 |
rs762300866 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8952726 | CATGGACACCTTTCC[C/G]GGGATGGGAGCATCA | 7874 |
rs762330474 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8958503 | CAGGCAGGCTGGAAG[C/T]AGGACCAAGAGGGAG | 7874 |
rs762335665 | snp | A/G | 3.29886e-05 | 0.00406118 | intron-variant | USP7 | GRCh38.p7 | 16:8910711 | ATAAAGAAGAACGCT[A/G]CAACAGGACACTAGC | 7874 |
rs762349192 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893584 | TATAACTGAAGGAAA[C/T]AGGTCAGACGAGCCT | 7874 |
rs762350954 | in-del | -/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8948771 | GCCAAAAACAAGCAT[-/G]GAAAACACAGCGAAA | 7874 |
rs762360435 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8930507 | ATTAATAAATTCCAA[C/T]TGTACCACAATAAAG | 7874 |
rs762364884 | snp | A/T | 4.97847e-05 | 0.00498897 | intron-variant | USP7 | GRCh38.p7 | 16:8894653 | AAACTAAAAGAAAAA[A/T]AATTAAAACTCCTCC | 7874 |
rs762422542 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8927239 | AGGCAGGAGAATCGC[C/T]TGAACCCGGGAGGCA | 7874 |
rs762436913 | snp | G/T | 0.000181475 | 0.00952389 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8921163 | GTTACTTACACTCCA[G/T]GCCATAAAATTGGAA | 7874 |
rs762450851 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8960135 | GGCCACCAAAGTTAG[C/T]GAATAAATAATACAC | 7874 |
rs762458977 | snp | C/T | 1.64844e-05 | 0.00287087 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8902187 | CACTGAGCTCAATCA[C/T]CTATTTCCAAAAGAG | 7874 |
rs762465941 | snp | A/G | 1.64917e-05 | 0.00287151 | intron-variant | USP7 | GRCh38.p7 | 16:8905381 | AGCACTGTGACAAGT[A/G]CCCAACACTAGAAGG | 7874 |
rs762468109 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8909488 | ATACAGTCTGAAAGA[C/T]AAAAGGATTCTGTCT | 7874 |
rs762482824 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8928286 | GAGGTGCTTCCCAGA[C/T]TGTGTGCCCTAGTCT | 7874 |
rs762501283 | snp | A/C | 1.72746e-05 | 0.00293888 | intron-variant | USP7 | GRCh38.p7 | 16:8921327 | TCTGAGCCTTAGTTG[A/C]CATTATTTACCAGAT | 7874 |
rs762513974 | snp | C/G | 1.78058e-05 | 0.00298372 | intron-variant | USP7 | GRCh38.p7 | 16:8902358 | CACGGTTCCAAACCA[C/G]ATACGCTATTAACAA | 7874 |
rs762591755 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8933322 | GGGGCCAAGACGGGA[C/T]GATCACATAAGTCAA | 7874 |
rs762597278 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8913926 | GCTAATTTGTAGAGA[C/T]GGAGTCTCACTATGT | 7874 |
rs762632614 | snp | A/G | | | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8910824 | TCCACAAATGATTCA[A/G]ATACTTTAAAGAGAG | 7874 |
rs762642145 | in-del | -/TA | | | intron-variant | USP7 | GRCh38.p7 | 16:8929018 | GCTCCGCCCTATATC[-/TA]TATGTCTCCTCCCAA | 7874 |
rs762658376 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8926089 | AACCCGGGAGGCGAA[A/G]CTTGCAGTGAGCTGA | 7874 |
rs762664042 | snp | A/C/G | 7.95219e-05 | 0.0063052 | intron-variant, missense, stop-gained | USP7 | GRCh38.p7 | 16:8894511 | CTTGTTTCTTAGTCT[A/C/G]AAACCCACACCAGCC | 7874 |
rs762679680 | snp | A/G | 0.000131778 | 0.00811614 | intron-variant | USP7 | GRCh38.p7 | 16:8895022 | ACTCGGCCAACCACA[A/G]CAGCATACCTGGTGT | 7874 |
rs762705416 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8900059 | AGACCCAGACGCAGT[C/G]TCTTGCCCACAGACC | 7874 |
rs762715688 | snp | A/G | 0.000133896 | 0.00818107 | intron-variant | USP7 | GRCh38.p7 | 16:8936555 | TCCATCACCAGCATA[A/G]GGAGCTCAACCTGAA | 7874 |
rs762752076 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894087 | GCCCTAGCCAAGGCC[A/G]AGGATGAGACATATT | 7874 |
rs762766564 | in-del | -/T | 3.30327e-05 | 0.0040639 | intron-variant | USP7 | GRCh38.p7 | 16:8902222 | GATTTTAGAAGAGTC[-/T]TAATGGCTTAGGTGA | 7874 |
rs762801682 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8909928 | GAGTCTCCGTCTCAG[A/G]AAAAAAAGCAACTTT | 7874 |
rs762829947 | in-del | -/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8929306 | ACACCATTGCCCTCG[-/T]TCTACGGTGGAAAGC | 7874 |
rs762840813 | snp | A/G | 1.64781e-05 | 0.00287033 | synonymous-codon, intron-variant | USP7 | GRCh38.p7 | 16:8904534 | CAACTGCTGAGGAAT[A/G]TCATGGTCGGTGACC | 7874 |
rs762842241 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950643 | AACCCAGCCCTGTCT[A/G]CCACGAACATGGCAC | 7874 |
rs762857182 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8915481 | TTTGGGTATGGTGCC[C/T]TCTACACAGGTGCCT | 7874 |
rs762870462 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8940170 | ATGCTCTCACAAACA[G/T]CTCTGTCCTGTGGCT | 7874 |
rs762884868 | snp | A/G | 1.6477e-05 | 0.00287024 | intron-variant | USP7 | GRCh38.p7 | 16:8894748 | AAGGCTTGAGCCTAT[A/G]GCCCGCCAAGCCCCC | 7874 |
rs762918678 | in-del | -/AG | 1.64879e-05 | 0.00287118 | intron-variant | USP7 | GRCh38.p7 | 16:8905153 | GTCCAAGTCCACCAC[-/AG]TAAAGAACAGAACAA | 7874 |
rs762920286 | snp | A/G | 1.65688e-05 | 0.00287821 | intron-variant | USP7 | GRCh38.p7 | 16:8899191 | CTGTCTTTGCAACCT[A/G]AGACACAGAAAGGAA | 7874 |
rs762934865 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8949753 | ATGCTGGCTTTCCTT[A/C]CGCAGAGACACCTTA | 7874 |
rs763018700 | snp | C/T | 1.66098e-05 | 0.00288177 | intron-variant | USP7 | GRCh38.p7 | 16:8903257 | GGTATATCCACGGGA[C/T]CGGTACGCACCATGG | 7874 |
rs763025381 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8895425 | ACAGCTCTAAATTCA[A/G]GTGATCCACAGTTTC | 7874 |
rs763089489 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8930772 | CCAGGAGTTCGAGAC[C/T]AGGCTGGCCAACATG | 7874 |
rs763097638 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8916321 | ACCTTCAAATCCCTA[C/T]TCAAGTAATTCTTAC | 7874 |
rs763099581 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8907372 | AAGACTGTGAATGGG[C/T]GACCAAAGCCTCAGC | 7874 |
rs763120614 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8939748 | TACTATTCACATTAC[A/G]TGGGTAAGTTTAATA | 7874 |
rs763125058 | snp | C/T | 1.66134e-05 | 0.00288208 | intron-variant | USP7 | GRCh38.p7 | 16:8894667 | AAAATTAAAACTCCT[C/T]CGTTATTTCTGTATA | 7874 |
rs763125309 | snp | C/T | 1.64993e-05 | 0.00287218 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8908388 | AGGGTCATACATAAA[C/T]CTCATCAGTTGTAGA | 7874 |
rs763147871 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8949340 | TAAAAATGCAATGCA[A/G]TTGATTGTTGGGTAC | 7874 |
rs763159551 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8917743 | AACAAAATCAGCCCC[C/G]AGAGAACTACTTTTA | 7874 |
rs763191260 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8906108 | ATGCGACCAGCCAGC[A/C]TCCCCGACTGGGCCC | 7874 |
rs763193864 | snp | A/G | 1.6777e-05 | 0.00289624 | intron-variant | USP7 | GRCh38.p7 | 16:8917203 | CTGAGAAGATGCAGG[A/G]GAATTTAAAAAACAG | 7874 |
rs763233051 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8948338 | CAAGCACACGCCATC[A/G]TGGCTGACTAATTTT | 7874 |
rs763246042 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8925690 | CTGCCCTGACACACA[A/G]TGGTTAGTTCACAAT | 7874 |
rs763254962 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8913302 | TGGAGGTTGCAGTGA[G/T]CCGAGATCGCACCAC | 7874 |
rs763307116 | snp | C/T | 3.30557e-05 | 0.00406531 | intron-variant | USP7 | GRCh38.p7 | 16:8898460 | GAAAAGAAAGATTCA[C/T]ATCAGATACCGTCAC | 7874 |
rs763321777 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957711 | TGCAGTGAGCTATGA[C/T]CGCCCACTGCACTAC | 7874 |
rs763326788 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8932293 | ATTTCTGGTCCGACC[C/G]GTGGCTCACTGCCTA | 7874 |
rs763346677 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8922066 | TGCTTCAGGCTAAAG[C/T]TGTCCATCGGACTAA | 7874 |
rs763347129 | snp | A/G | 4.94181e-05 | 0.00497057 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8905269 | ATCGTGACCCCCATA[A/G]TTGTGCTCAATTGCT | 7874 |
rs763373713 | in-del | -/GT | | | intron-variant | USP7 | GRCh38.p7 | 16:8947989 | GGAAGCTTGGACATG[-/GT]GTGACAGGCACTTTG | 7874 |
rs763404307 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8955060 | TGGTGTGTGGACCAG[A/T]CACTATTAATCACCT | 7874 |
rs763404579 | snp | A/C | 1.68386e-05 | 0.00290155 | intron-variant | USP7 | GRCh38.p7 | 16:8900508 | TAGTACAAAGTGATA[A/C]AATCCTTCACAAAGT | 7874 |
rs763435735 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8965137 | TCTCCCTATACCCGC[G/T]TTCCCTGCATTTTTC | 7874 |
rs763440545 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8944778 | TTCAAGGGCTGTCAG[A/C]TCTTTTGAAAAACTA | 7874 |
rs763489843 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8898249 | CCCCCATCATGTGCT[A/G]TTGTTTAGAGTGTTT | 7874 |
rs763503448 | snp | C/T | 3.29853e-05 | 0.00406098 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8903367 | ATCGTACATGTCATT[C/T]CCTTGGTGGCCACAA | 7874 |
rs763628128 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8902289 | GTCCAATTCTAGTTA[A/G]GTGGACCAAAAGGGA | 7874 |
rs763633806 | snp | G/T | 1.64914e-05 | 0.00287149 | intron-variant | USP7 | GRCh38.p7 | 16:8905139 | TTCATGGTACAAATG[G/T]CCAAGTCCACCACAG | 7874 |
rs763659511 | in-del | -/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8933505 | TTACAAAATTCAAAA[-/G]ATGTCTACAGAAACA | 7874 |
rs763660833 | snp | C/T | 1.76855e-05 | 0.00297362 | utr-variant-5-prime, intron-variant | USP7 | GRCh38.p7 | 16:8936667 | GGGAGGTTCTCTCAC[C/T]CACATCAGAGTGACT | 7874 |
rs763704468 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8942433 | CTGCAGCACTGTGAG[G/T]GTCTGACCACCTGCA | 7874 |
rs763716146 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8901591 | CTTGTGTCTTTGCCA[A/G]AAGTGACCACTCACA | 7874 |
rs763719614 | snp | A/G | 6.59424e-05 | 0.00574168 | missense, intron-variant | USP7 | GRCh38.p7 | 16:8904550 | TCATGGTCGGTGACC[A/G]CCTGTAAAACTTCAC | 7874 |
rs763721668 | snp | G/T | 1.6483e-05 | 0.00287076 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8916507 | TGAAACTTACCACTC[G/T]ACAAAGCTCCTGAAC | 7874 |
rs763723410 | in-del | -/CC | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938106 | CTGGCAAAGGCACTG[-/CC]ACAAGAGGCCCTAGG | 7874 |
rs763730572 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8911853 | AAGAACCAGCAAGAG[A/G]ATGAGGATTGGGGGG | 7874 |
rs763738080 | snp | C/T | 1.66529e-05 | 0.00288551 | intron-variant | USP7 | GRCh38.p7 | 16:8915537 | GCAACTGAAAAAGAA[C/T]GTTTTGGCTTTAAAA | 7874 |
rs763769764 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8919694 | CCACCCCCACCCCAA[A/G]TAGTAAAAGGAAGCC | 7874 |
rs763784425 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8921299 | CAAGACCATGACCTG[C/T]TTAAAAGAATAATCT | 7874 |
rs763820833 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8911102 | CGAACAAAGCACATA[A/C]TGTAAAGCTATGATT | 7874 |
rs763868487 | snp | C/T | 3.30491e-05 | 0.00406491 | intron-variant | USP7 | GRCh38.p7 | 16:8898470 | ATTCACATCAGATAC[C/T]GTCACCAAAACCCCG | 7874 |
rs763921431 | snp | C/T | | | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891925 | CAGAGGGAGAGGACA[C/T]AATAGTCCCAGGGGT | 7874 |
rs763936930 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8948925 | GCTATGATCAAACCA[C/T]GGCACTCCAGCCTGG | 7874 |
rs763956207 | snp | C/T | 1.65614e-05 | 0.00287757 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8920364 | AAAAACTTACGCAAC[C/T]CCATGGGGAGCATCC | 7874 |
rs763956429 | snp | A/G | 1.64781e-05 | 0.00287033 | intron-variant | USP7 | GRCh38.p7 | 16:8901134 | AGGTAAGTGCACGAA[A/G]GACTTACGTATTTTA | 7874 |
rs763964508 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8958091 | GAGCATCTCCCACAA[A/G]TAAATTTAACAAAAA | 7874 |
rs763996053 | snp | A/G | 3.29538e-05 | 0.00405904 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8910766 | GCCATGTTCCCCAGC[A/G]TCGTATTTATTGTCC | 7874 |
rs764004472 | snp | A/G | 1.67708e-05 | 0.00289571 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8898627 | AAGAGGATTACCTGG[A/G]CCATCCCTATAACTA | 7874 |
rs764024617 | snp | A/G | 1.6528e-05 | 0.00287467 | intron-variant | USP7 | GRCh38.p7 | 16:8902033 | AACAACAATCCAGGA[A/G]TCCAACGCTACTGCT | 7874 |
rs764029067 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8958706 | TTCCCCACACTCATC[A/G]CAGGGAGCTCTAGCA | 7874 |
rs764050052 | snp | C/T | 1.6604e-05 | 0.00288127 | intron-variant | USP7 | GRCh38.p7 | 16:8894677 | CTCCTCCGTTATTTC[C/T]GTATATCAGCAAAAC | 7874 |
rs764050487 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8934770 | ATGGCAAAGGGCCAC[C/T]GGTTGGCCACCGAGT | 7874 |
rs764059923 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8948414 | GATCTCAAACCCCTG[A/G]GCTCAAGCTATCCAC | 7874 |
rs764062309 | snp | C/T | | | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8898433 | TCTGTGATTTTCATC[C/T]TAAGCTATTAAGAAA | 7874 |
rs764072063 | in-del | -/TA | 4.54514e-05 | 0.00476693 | intron-variant | USP7 | GRCh38.p7 | 16:8895778 | TAGGGCAAAATGAAG[-/TA]TATATATATTCACAT | 7874 |
rs764083618 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8925235 | AAGACACTATGCACA[C/G]TGACCTGACTCTGGT | 7874 |
rs764125496 | snp | C/T | 1.74151e-05 | 0.0029508 | intron-variant | USP7 | GRCh38.p7 | 16:8920476 | ATAAGAATATCCAGC[C/T]TGAATAAGAACACAC | 7874 |
rs764139280 | snp | C/T | 3.30262e-05 | 0.0040635 | intron-variant | USP7 | GRCh38.p7 | 16:8897116 | TAAGTAATGAAAAGA[C/T]AAAATAAGTGCTTTC | 7874 |
rs764157081 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8956014 | GATGGGACCATGTTC[C/T]GCAATACAAGTCACA | 7874 |
rs764167225 | snp | G/T | 1.69815e-05 | 0.00291384 | intron-variant | USP7 | GRCh38.p7 | 16:8900661 | TAAAATTGTTACACT[G/T]CAAGTTTGTCTAACG | 7874 |
rs764230617 | in-del | -/AAAA | 2.46685e-05 | 0.00351193 | intron-variant | USP7 | GRCh38.p7 | 16:8906626 | AGTATTAATTTACAC[-/AAAA]AATATCACACTTTAC | 7874 |
rs764274530 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8924201 | TTTGCATGTGGCCAT[C/T]GGTCAATCACCTTTG | 7874 |
rs764296646 | snp | A/C | 0.00013861 | 0.0083238 | intron-variant | USP7 | GRCh38.p7 | 16:8936548 | ATCTCCATCCATCAC[A/C]AGCATAAGGAGCTCA | 7874 |
rs764339209 | snp | A/G | 4.94173e-05 | 0.00497053 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8895073 | TCCGAACGTTCCGAA[A/G]ACCTCTTTGTGGAAA | 7874 |
rs764364415 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8922768 | CATTTCATAATATAC[A/G]TGAATGTTTAAATGT | 7874 |
rs764397590 | snp | A/T | 1.65031e-05 | 0.00287251 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8900554 | ACTATGATGTCACCA[A/T]CCATTAGTTCATCAA | 7874 |
rs764439096 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8903659 | ATCACCTGAGGTCAG[A/G]AGTTCCGAGACCAGC | 7874 |
rs764450626 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8932311 | GGCTCACTGCCTATA[A/G]TCCTAGCACTCTGGG | 7874 |
rs764528178 | snp | A/T | 1.65119e-05 | 0.00287327 | intron-variant | USP7 | GRCh38.p7 | 16:8899593 | AGAGGAAAGGAGCAT[A/T]TATTAAATACCTGAA | 7874 |
rs764533568 | snp | C/G/T | 4.99532e-05 | 0.00499745 | intron-variant, missense | USP7 | GRCh38.p7 | 16:8894544 | CGGGGGGGGGAGAAC[C/G/T]CTTACCGGGCTGTGG | 7874 |
rs764550404 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8951127 | ACAGGCAAGGCTTAA[A/T]GTCAAACCAAGTAAG | 7874 |
rs764570050 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8903967 | CTAGACAGCCAACGG[C/T]GAGATGACCTCCTCC | 7874 |
rs764618068 | snp | A/T | 2.09225e-05 | 0.00323432 | intron-variant | USP7 | GRCh38.p7 | 16:8902512 | AAGAGTAGATTAAAA[A/T]AAAAACACGCTCATA | 7874 |
rs764625633 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938035 | TCGTCACTGGCCCCA[G/T]GGTAAGGCAGGGCAG | 7874 |
rs764633889 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8947159 | ACACTGCAGCTGACT[A/G]AATGCACAAGCAGGT | 7874 |
rs764640621 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8928729 | CTTCTCGGATTATAC[A/G]CTTTTTCCATCAAGG | 7874 |
rs764642506 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961861 | TTGCTGCTTTGCTGG[A/G]GCCAAGTGAAACAGA | 7874 |
rs764670129 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8936279 | TCTCTGGGTGGCTCA[C/T]ATGGCGCCCTACAGC | 7874 |
rs764723797 | snp | A/G | 1.64849e-05 | 0.00287092 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8915318 | TCTATCAGACCGATA[A/G]TCTACTTCTTTACAC | 7874 |
rs764725226 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8958782 | AGTGGCGCATGGCAC[A/C]AAATCCACTTGACTT | 7874 |
rs764768299 | snp | C/T | 4.96085e-05 | 0.00498014 | intron-variant | USP7 | GRCh38.p7 | 16:8902039 | AATCCAGGAATCCAA[C/T]GCTACTGCTCTAAGT | 7874 |
rs764781517 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892767 | CTTCCACGTAACTCA[C/G]TGAATTATAATTTTT | 7874 |
rs764793771 | snp | C/G | 1.76602e-05 | 0.0029715 | intron-variant | USP7 | GRCh38.p7 | 16:8920484 | ATCCAGCTTGAATAA[C/G]AACACACATTTTATT | 7874 |
rs764817274 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8926352 | GGTGTGGTGGTGCAC[A/G]CCTGTAATCCCAGCT | 7874 |
rs764858801 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8901161 | TTTACAGGATATTGG[C/T]GTGTAGATATGCCCA | 7874 |
rs764869358 | snp | A/G | | | downstream-variant-500B, nc-transcript-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8892004 | CAGCTTGTCTCCCCA[A/G]AACCAGTTTAACAAA | 7874 |
rs764875163 | snp | C/G | 1.6483e-05 | 0.00287076 | intron-variant | USP7 | GRCh38.p7 | 16:8905162 | CACCACAGTAAAGAA[C/G]AGAACAAAAGTGAAC | 7874 |
rs764893136 | snp | A/C | 1.64833e-05 | 0.00287078 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893962 | TTAAGGGGCCACCCA[A/C]ACACCGTCCTCGCCT | 7874 |
rs764905318 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8935419 | TTTCACCACGTTGGC[A/C]AGGCTGGTCTCGAAC | 7874 |
rs764946216 | snp | C/T | 1.65211e-05 | 0.00287407 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8917037 | ATACCCAAATGACTT[C/T]GTTAACTTTTTTGTT | 7874 |
rs765014003 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8898896 | CATGGGAGATGCACT[C/G]AGGATGTATCTAAAG | 7874 |
rs765030698 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8944434 | TCTCTTAAATGTCTG[C/T]TTTTCCCTAAAAATT | 7874 |
rs765049910 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8908673 | CAGCACTGACTGTGA[G/T]AGATTCTCTTACCTT | 7874 |
rs765067130 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8940976 | TAGCAGGACAGAATT[A/C]TCTCTCCTCCCACTC | 7874 |
rs765073240 | in-del | -/AA | 1.65611e-05 | 0.00287755 | intron-variant | USP7 | GRCh38.p7 | 16:8897142 | CTTTCAAGAAAGCAT[-/AA]AAGGTCTGCTACCAC | 7874 |
rs765099326 | in-del | -/CAAA | 1.66829e-05 | 0.00288811 | intron-variant | USP7 | GRCh38.p7 | 16:8901268 | AGTTTTGTTAAGATC[-/CAAA]CACTCAGCACAATGC | 7874 |
rs765111712 | snp | A/G | 3.43974e-05 | 0.00414699 | intron-variant | USP7 | GRCh38.p7 | 16:8898642 | GCCATCCCTATAACT[A/G]CACAAGAAAACAGCA | 7874 |
rs765133044 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8952239 | TGGGCACGAGGGAGA[A/G]CCTGTCTCCAAAAAA | 7874 |
rs765136760 | in-del | -/TGGAGAGACCT | | | intron-variant | USP7 | GRCh38.p7 | 16:8923732 | CAGGCACCAAGTGAG[-/TGGAGAGACCT]TGGAGAGAAGGAACG | 7874 |
rs765137683 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8918792 | CCAGCCTGGGCGACA[C/G]AGCAAGACTCCATCT | 7874 |
rs765138075 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8949076 | GGTGATGAAAATGTG[C/G]TCGAATTGAATGCTG | 7874 |
rs765139784 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8907625 | CTTTGGGAGGCTGAG[A/G]CCGGCAGATCACTTG | 7874 |
rs765140671 | snp | C/G | 1.64789e-05 | 0.0028704 | intron-variant | USP7 | GRCh38.p7 | 16:8894892 | GCTCACACAGTCACT[C/G]CCAGCACCCCCAGGC | 7874 |
rs765159174 | snp | A/C | 1.65048e-05 | 0.00287265 | intron-variant | USP7 | GRCh38.p7 | 16:8899091 | AAGCATGCAGTCAAG[A/C]CCAAGCAAGTGTCCA | 7874 |
rs765162773 | snp | A/G | 1.64768e-05 | 0.00287021 | intron-variant | USP7 | GRCh38.p7 | 16:8894886 | ACATGTGCTCACACA[A/G]TCACTCCCAGCACCC | 7874 |
rs765175569 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8933025 | GGCTCACTGCAACCT[C/G]TGCCTCCGGGGTGCC | 7874 |
rs765203410 | snp | A/G | | | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962165 | AGCTTCATTCATTGA[A/G]GCAACCCAAGATCCC | 7874 |
rs765229568 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8918042 | TGATCCGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 7874 |
rs765270151 | snp | C/T | 1.65241e-05 | 0.00287433 | intron-variant | USP7 | GRCh38.p7 | 16:8921146 | TTCAGACTAAATACA[C/T]TGTTACTTACACTCC | 7874 |
rs765278399 | in-del | -/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8939915 | CCATCCTGGCTAACA[-/C]GGTGAAACCCCGACT | 7874 |
rs765289168 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8939002 | GGGACAGGGAGAGAT[C/G]CCATACCCTTTTCCT | 7874 |
rs765299616 | snp | C/T | 6.6411e-05 | 0.00576204 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8894554 | AGAACCCTTACCGGG[C/T]TGTGGCTCAAAGTCT | 7874 |
rs765308110 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8947231 | AAATGTAAAGCAATG[C/T]CATTCCTCTCAATAC | 7874 |
rs765312006 | snp | C/T | 3.37741e-05 | 0.00410925 | intron-variant | USP7 | GRCh38.p7 | 16:8898311 | GACAGGTAGAAACAA[C/T]AAGCAAGTTCCAATA | 7874 |
rs765337096 | snp | A/C | 1.6609e-05 | 0.0028817 | intron-variant | USP7 | GRCh38.p7 | 16:8894659 | AAAGAAAAAAAATTA[A/C]AACTCCTCCGTTATT | 7874 |
rs765352266 | snp | G/T | 1.65012e-05 | 0.00287234 | intron-variant | USP7 | GRCh38.p7 | 16:8908337 | ATATCCCACTATAGA[G/T]TACCTATCATTGATC | 7874 |
rs765391538 | snp | C/G | 6.89489e-05 | 0.00587109 | utr-variant-5-prime, intron-variant | USP7 | GRCh38.p7 | 16:8936640 | TCTGCAGTGGCCTCT[C/G]CTGGGGGATGGGGGA | 7874 |
rs765399923 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956922 | CTGGGCAGCACAACA[C/T]AGACAAGTCGACGCT | 7874 |
rs765410131 | in-del | -/ACA | 1.6495e-05 | 0.0028718 | intron-variant | USP7 | GRCh38.p7 | 16:8910711 | ATAAAGAAGAACGCT[-/ACA]ACAGGACACTAGCAC | 7874 |
rs765437211 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8916189 | TGACTCAGGACCAAC[A/G]GGACAGCCAACAAAG | 7874 |
rs765439237 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8905449 | CCCTAGTTGAAAAAA[C/T]ATCCATGTGTGTTCT | 7874 |
rs765440096 | snp | A/T | 1.66871e-05 | 0.00288847 | intron-variant | USP7 | GRCh38.p7 | 16:8920337 | GACATTTTTAACAGC[A/T]CCTGATTAAAGAAAA | 7874 |
rs765451177 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8947243 | ATGCCATTCCTCTCA[A/G]TACACTTTTGGAAAA | 7874 |
rs765458565 | snp | A/T | 1.64849e-05 | 0.00287092 | intron-variant | USP7 | GRCh38.p7 | 16:8919152 | CACCTGAAAGATCAG[A/T]TCAAGGTTGAGGGGA | 7874 |
rs765500463 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8902592 | TATATAGTCAATGTT[-/A]AAGACTGTGATCGTA | 7874 |
rs765516848 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8946530 | AATATCTGCAAATCG[C/T]GTATCTTACAAAGAC | 7874 |
rs765536244 | snp | A/G | | | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8915459 | CCACCATTTTGCCGC[A/G]GAATAATTTGGGTAT | 7874 |
rs765562437 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8896826 | ACTGGAGCAACACTG[C/G]GTCTGTGTTGAGCTT | 7874 |
rs765565739 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8924348 | CAGCAAAGTCAACAT[G/T]CTACACAAGCTTCTA | 7874 |
rs765588791 | snp | C/G/T | 0.000131801 | 0.00811693 | intron-variant | USP7 | GRCh38.p7 | 16:8899776 | GTGGAGGGAGAAAGT[C/G/T]TGCAGTCTGAATCAA | 7874 |
rs765608418 | snp | A/C | 1.66468e-05 | 0.00288498 | intron-variant | USP7 | GRCh38.p7 | 16:8903252 | GGTGGGGTATATCCA[A/C]GGGACCGGTACGCAC | 7874 |
rs765653626 | in-del | -/TAAAAA | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892606 | TGACTAGTTAGAGGC[-/TAAAAA]AAAAAAAAAAAAAAA | 7874 |
rs765676424 | snp | A/T | 3.2975e-05 | 0.00406035 | intron-variant | USP7 | GRCh38.p7 | 16:8895638 | CAGTATCGGGGACAG[A/T]TACCTCTATTCGAAA | 7874 |
rs765688158 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8930464 | GAATAAGCAAAATAT[A/G]AACTTATACTTTTGA | 7874 |
rs765690867 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8943554 | AGAAACACAAACGAC[C/T]AACCAACAGGCTCCA | 7874 |
rs765726067 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8920585 | CAACTTTTTTGCTAA[A/T]TTTAGACTGTTTCAA | 7874 |
rs765745616 | in-del | -/CCCATG | | | intron-variant | USP7 | GRCh38.p7 | 16:8941131 | ACATGGGGCCCATGC[-/CCCATG]CCCATGAGGACCCCC | 7874 |
rs765762500 | snp | C/G | | | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8895667 | AACGTCCGGCTCGTT[C/G]CAGGAGATAAACATT | 7874 |
rs765780543 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8952784 | TAGTCACAGAGTCTG[A/G]CAGTTCCCAAACTCA | 7874 |
rs765786478 | snp | C/T | 3.29506e-05 | 0.00405884 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8899631 | CATTCTATTTGATAA[C/T]GTAACCACAAATCCA | 7874 |
rs765815952 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8939716 | CGTGCACTTTTTCTC[A/G]TGAAGGAAAACACAT | 7874 |
rs765853664 | snp | C/T | 3.29663e-05 | 0.00405981 | intron-variant | USP7 | GRCh38.p7 | 16:8894900 | AGTCACTCCCAGCAC[C/T]CCCAGGCCACGTCAC | 7874 |
rs765881357 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8942710 | ACACCACCACACTCA[A/G]CTAGTTTCTGTATTT | 7874 |
rs765920458 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8918893 | CTGGGGAATGAAAAC[A/G]CAGCATGAACTAGCA | 7874 |
rs765929914 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8924262 | AACGACTCCTGCGAA[A/G]GCACAGTCCTCCCAC | 7874 |
rs765934502 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8892845 | ATACAGGAAGAGTTG[C/G]TGTACACTGCTCCCA | 7874 |
rs765957329 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893698 | CAGAGACCTTGAGCC[A/T]GGGACCCCCGATCCA | 7874 |
rs765958236 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8949218 | GAATTTTATCAAAAA[A/G]CACAGATGCAAATCT | 7874 |
rs765969817 | in-del | -/TT | | | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891789 | TTCAGCTCGCTGCTC[-/TT]GTGTGTGAGGGCGTG | 7874 |
rs765975143 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8958999 | CCTGTGGTGTGTGCC[C/G]CACTTTAGTTCTAAC | 7874 |
rs765988791 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8928295 | CCCAGATTGTGTGCC[C/G]TAGTCTGAAATGGAC | 7874 |
rs766002322 | snp | A/G | 1.64966e-05 | 0.00287194 | intron-variant | USP7 | GRCh38.p7 | 16:8902202 | TCTATTTCCAAAAGA[A/G]ACGCTGATTTTAGAA | 7874 |
rs766023368 | snp | C/T | 1.64893e-05 | 0.0028713 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8921173 | CTCCAGGCCATAAAA[C/T]TGGAAAATCCCCAAT | 7874 |
rs766047948 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8903711 | TGTCTCTACTAAAAA[C/T]ACAAAATTAGCTGGG | 7874 |
rs766054404 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8903079 | GGGTTCCCCTGTGCA[G/T]GAGTCAGGGGCTCAA | 7874 |
rs766083555 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8927330 | AAAAAGAAAAAAAAA[A/G]AGAAAGAAAGTTAAA | 7874 |
rs766091523 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8952559 | TGCACCTGTCTTCTC[A/G]GGTCCCCTCACTCTG | 7874 |
rs766178754 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8936416 | ATGACTTAAAATAGA[A/G]GCTACAGAGGTAAAC | 7874 |
rs766193921 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8900090 | TGACAGGTGGTGGAG[C/T]CCAGTCTCTGACCGT | 7874 |
rs766194708 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8909989 | TGGACTGACCTAGCA[C/G]AAGAGTACATTTGGA | 7874 |
rs766214062 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8933486 | ATATAATTTCATATT[C/T]CCTTTACAAAATTCA | 7874 |
rs766233523 | snp | A/G | 1.64841e-05 | 0.00287085 | intron-variant | USP7 | GRCh38.p7 | 16:8915364 | AAATAAGGAAAGTAA[A/G]AGTGGTTTAACTAGT | 7874 |
rs766256394 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8954654 | AATACGAAGGTATGT[A/T]TTCATTTGAGGTTTG | 7874 |
rs766257822 | in-del | -/ATATGTTCTTGATAAAAAGATA | | | intron-variant | USP7 | GRCh38.p7 | 16:8917685 | CACCCAGCCTCACCC[-/ATATGTTCTTGATAAAAAGATA]ATACAGAAAAAGTAA | 7874 |
rs766263622 | snp | C/T | 1.64732e-05 | 0.0028699 | splice-donor-variant | USP7 | GRCh38.p7 | 16:8895030 | AACCACAACAGCATA[C/T]CTGGTGTATCCTCAG | 7874 |
rs766321599 | snp | C/T | 1.70746e-05 | 0.00292182 | intron-variant | USP7 | GRCh38.p7 | 16:8900667 | TGTTACACTGCAAGT[C/T]TGTCTAACGTTTAAT | 7874 |
rs766321600 | snp | C/T | 1.64784e-05 | 0.00287035 | missense, intron-variant | USP7 | GRCh38.p7 | 16:8904536 | ACTGCTGAGGAATAT[C/T]ATGGTCGGTGACCGC | 7874 |
rs766397638 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8908963 | CTCTTTGATGTTTGC[A/G]TAAGAACCCATATAT | 7874 |
rs766407371 | snp | C/T | 1.66788e-05 | 0.00288775 | intron-variant | USP7 | GRCh38.p7 | 16:8904413 | CATGGTGACCCGGAG[C/T]CCCAGAAGGGCGGGG | 7874 |
rs766435653 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8929162 | CAAGTGGCTAGAATT[C/G]ATCCCAAACGCACAC | 7874 |
rs766464272 | snp | C/T | 1.66161e-05 | 0.00288232 | intron-variant | USP7 | GRCh38.p7 | 16:8894668 | AAATTAAAACTCCTC[C/T]GTTATTTCTGTATAT | 7874 |
rs766468212 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8939762 | CGTGGGTAAGTTTAA[C/T]AACTCCAAAACATTG | 7874 |
rs766526952 | snp | C/T | 0.000371609 | 0.0136259 | intron-variant | USP7 | GRCh38.p7 | 16:8929571 | CAACCCTCATGAGGA[C/T]TGATGGACATGCTTT | 7874 |
rs766578714 | snp | G/T | 3.05507e-05 | 0.00390825 | intron-variant | USP7 | GRCh38.p7 | 16:8902531 | AACACGCTCATATTT[G/T]AGTCCTCTATATTAC | 7874 |
rs766578819 | snp | C/G | 1.64844e-05 | 0.00287087 | intron-variant | USP7 | GRCh38.p7 | 16:8910737 | CTAGCACAAAACACT[C/G]AATTTACCTGTAAGC | 7874 |
rs766586267 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8907403 | TGGTAGCAAGTAAAG[G/T]GATTTGATTACACTC | 7874 |
rs766595112 | snp | A/C | 1.65647e-05 | 0.00287786 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8908418 | ATGTAACACTGGTGG[A/C]AATGTTAGGAATTTC | 7874 |
rs766598816 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8896238 | AAGCATAAGATTAAA[A/G]GGCTCTGCTGGACAA | 7874 |
rs766676233 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8906126 | CCCGACTGGGCCCAC[C/T]GCATGGGTAATTATC | 7874 |
rs766695028 | in-del | -/AGAG | | | intron-variant | USP7 | GRCh38.p7 | 16:8932619 | TGCTAAATTTAAAAA[-/AGAG]AGAGAAAGAAAAGAA | 7874 |
rs766726571 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8955079 | TATTAATCACCTATA[A/C]CCACTTTCTATGAAT | 7874 |
rs766728373 | snp | A/G | 1.67936e-05 | 0.00289767 | intron-variant | USP7 | GRCh38.p7 | 16:8900510 | GTACAAAGTGATACA[A/G]TCCTTCACAAAGTAC | 7874 |
rs766758828 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8913352 | CAGAGCGAGACTCCC[C/T]CTCAAAAAGAGGAGA | 7874 |
rs766760174 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8948355 | GGCTGACTAATTTTT[C/G]GCATTTTTTTGTAGA | 7874 |
rs766828801 | snp | C/T | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894097 | AGGCCGAGGATGAGA[C/T]ATATTACCTGGTGGG | 7874 |
rs766843328 | snp | A/G | 1.64863e-05 | 0.00287104 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8895655 | ACCTCTATTCGAAAC[A/G]TCCGGCTCGTTGCAG | 7874 |
rs766848566 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8911964 | GACTCAGCTAACAAC[G/T]GAAAGGATGTGGGGA | 7874 |
rs766876530 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8910964 | GTAACTCTCCCCCTG[C/T]AGCCAAGACTGTAGG | 7874 |
rs766885309 | in-del | -/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8908890 | AATGCCCAAACAGAA[-/C]AAGCAGCAATGAACA | 7874 |
rs766896018 | snp | G/T | 1.68094e-05 | 0.00289904 | intron-variant | USP7 | GRCh38.p7 | 16:8917207 | GAAGATGCAGGGGAA[G/T]TTAAAAAACAGTAAG | 7874 |
rs766903386 | snp | A/T | 3.29772e-05 | 0.00406048 | intron-variant | USP7 | GRCh38.p7 | 16:8895181 | ACAGACACAGTTCTG[A/T]AAGTGCAAGTGATGT | 7874 |
rs766927347 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8954620 | AGAGATGAAGACTTG[A/C]CAAAAACTTTACTAA | 7874 |
rs766933364 | snp | C/T | 1.64789e-05 | 0.0028704 | intron-variant | USP7 | GRCh38.p7 | 16:8899796 | GTCTGAATCAAAGTC[C/T]ATGGCAGGGGGTAGC | 7874 |
rs766936467 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8921520 | TCACTCATGGTTTCA[C/T]TTTTTAATTCCTTAG | 7874 |
rs766972226 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8931543 | ATAATTATGTAAAGA[C/T]CCGGGAAAGTGTTTA | 7874 |
rs766980920 | snp | C/T | 1.64991e-05 | 0.00287215 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8915523 | TTCCACATTATCGAG[C/T]AACTGAAAAAGAATG | 7874 |
rs766986124 | snp | A/G | 3.29511e-05 | 0.00405887 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8917085 | ATGCTGTAATTCATA[A/G]AACACTCTTTGTAAT | 7874 |
rs766988453 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8900200 | TACATGAAGACAGAC[C/T]GAAATGAATTACCCA | 7874 |
rs767081100 | in-del | -/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8924161 | ATTTAAAATTCAATC[-/T]TTCACTGATGACAGT | 7874 |
rs767082582 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8910238 | CCTTCATCCAAGCGG[A/G]GGCTGGCCACCTGGT | 7874 |
rs767095320 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8949993 | TGTCTAAACAGCAGT[A/G]CTGTCCCACCAACCA | 7874 |
rs767095600 | snp | C/T | 1.65067e-05 | 0.00287282 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8899123 | ACATGTGACCTACCC[C/T]TGAGACTTGAAAAAC | 7874 |
rs767106969 | snp | A/G | 1.65976e-05 | 0.00288072 | intron-variant | USP7 | GRCh38.p7 | 16:8904425 | GAGTCCCAGAAGGGC[A/G]GGGGCTGACCTGCAC | 7874 |
rs767139024 | snp | A/C | | | intron-variant, missense | USP7 | GRCh38.p7 | 16:8894488 | CTGCCCCTCCCAGCC[A/C]CAGACCACTTGTTTC | 7874 |
rs767149020 | snp | C/T | 3.29468e-05 | 0.00405861 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8923331 | ATTTCGCACAAAACA[C/T]GGAGGGCTAAGGACC | 7874 |
rs767163734 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8920243 | GTGCCACAGGGCAAG[C/T]GCAGAGAGGAGGCTT | 7874 |
rs767165493 | snp | A/G | 1.78118e-05 | 0.00298422 | intron-variant | USP7 | GRCh38.p7 | 16:8921343 | CATTATTTACCAGAT[A/G]TTATACATTTTTAAA | 7874 |
rs767198934 | snp | C/G | 0.000131944 | 0.00812123 | intron-variant | USP7 | GRCh38.p7 | 16:8915378 | AAAGTGGTTTAACTA[C/G]TAATAGTCAAAAAAT | 7874 |
rs767223481 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961431 | CGGGAGACGGAGGTT[A/G]TAGTGACCCGAGATC | 7874 |
rs767291036 | snp | A/T | 4.99671e-05 | 0.00499811 | intron-variant | USP7 | GRCh38.p7 | 16:8920342 | TTTTAACAGCACCTG[A/T]TTAAAGAAAAACTTA | 7874 |
rs767305810 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8924487 | TGGAAGGCTGTTCCC[G/T]GCTTAGAATCAGGTG | 7874 |
rs767344359 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8925152 | CCACATTTTAGGTGA[A/G]GAAATGGAGGTTCGC | 7874 |
rs767346860 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8901456 | AAACATCAGACCCAT[C/G]GAAACCCACTACATT | 7874 |
rs767382398 | in-del | -/TAACAG | | | intron-variant | USP7 | GRCh38.p7 | 16:8910944 | GAAGGTAAACAACAC[-/TAACAG]TAACTCTCCCCCTGT | 7874 |
rs767383534 | snp | A/G | 1.64827e-05 | 0.00287073 | missense, intron-variant | USP7 | GRCh38.p7 | 16:8904544 | GGAATATCATGGTCG[A/G]TGACCGCCTGTAAAA | 7874 |
rs767390277 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8934396 | TTGAGAGAGACTGCA[C/T]TGTCTCCAAAAGTTA | 7874 |
rs767396671 | snp | C/T | 1.65285e-05 | 0.00287471 | intron-variant | USP7 | GRCh38.p7 | 16:8898463 | AAGAAAGATTCACAT[C/T]AGATACCGTCACCAA | 7874 |
rs767399360 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8939353 | CTATATAAATGGACA[C/T]AGTGTGGAATGAGTT | 7874 |
rs767428232 | snp | A/C/T | 8.3153e-05 | 0.00644751 | intron-variant | USP7 | GRCh38.p7 | 16:8904610 | CTGCAGATGGACTTT[A/C/T]CCCTCTTAGAAGCTC | 7874 |
rs767454460 | snp | A/G | 7.47468e-05 | 0.00611292 | utr-variant-5-prime, intron-variant | USP7 | GRCh38.p7 | 16:8936654 | TGCTGGGGGATGGGG[A/G]AGGTTCTCTCACCCA | 7874 |
rs767476344 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8918267 | GCTCCCTGCCCACCC[C/T]ACAACCAGGAGTGCC | 7874 |
rs767478172 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8933565 | AGGGTTACATAGAAG[C/T]AATGTAGTTTCTTCA | 7874 |
rs767486254 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8943399 | TGTGCAGCACAATGC[A/T]AGTAGAAGTTGCAGC | 7874 |
rs767486654 | snp | A/C/G | 8.41622e-05 | 0.00648651 | intron-variant | USP7 | GRCh38.p7 | 16:8898328 | AGCAAGTTCCAATAA[A/C/G]AATTAAAATTCATAG | 7874 |
rs767492711 | in-del | -/GAAAAAGCTGAAACTCATCTTTTCTGTA | | | intron-variant | USP7 | GRCh38.p7 | 16:8919504 | GGTCAGCACAACGTG[-/GAAAAAGCTGAAACTCATCTTTTCTGTA]GACACACACACAAGA | 7874 |
rs767501240 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957074 | GTGTATTTCCCCATA[C/G]AAGAAACGTACTAAT | 7874 |
rs767503046 | snp | A/G | 9.90181e-05 | 0.00703557 | intron-variant | USP7 | GRCh38.p7 | 16:8901069 | TCACCTAGGAGAAAG[A/G]AGATATTTTAAATGT | 7874 |
rs767549703 | in-del | -/TATC | | | intron-variant | USP7 | GRCh38.p7 | 16:8931039 | AGCGTAAAGAACCTT[-/TATC]TAATCATGCAAAGTC | 7874 |
rs767559815 | snp | A/C/G | 2.6348e-05 | 0.00362951 | intron-variant | USP7 | GRCh38.p7 | 16:8895786 | AAATGAAGTATATAT[A/C/G]TTCACATAAAAATAA | 7874 |
rs767573729 | snp | A/C/T | 6.63266e-05 | 0.00575843 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8903396 | AAAACTGGTCCTCTG[A/C/T]GACTATCTGAAAATA | 7874 |
rs767584240 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8955185 | ATTTGTTGTATTTAA[C/T]AAACTTGGGTTTCTC | 7874 |
rs767600368 | snp | C/T | 1.65438e-05 | 0.00287605 | intron-variant | USP7 | GRCh38.p7 | 16:8930288 | GGTGAACCACAGGCA[C/T]TTACCATCCTCCATG | 7874 |
rs767635734 | in-del | -/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8944232 | AGAGCAACAGAGGTG[-/C]AAAAAAAAAAAAGCA | 7874 |
rs767647532 | snp | A/C | 1.66247e-05 | 0.00288307 | intron-variant | USP7 | GRCh38.p7 | 16:8900526 | TCCTTCACAAAGTAC[A/C]TACTTCTGAAATACT | 7874 |
rs767652270 | snp | C/T | 8.23839e-05 | 0.00641757 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8917115 | TGCTAAAGGGACGCT[C/T]TTAGACGAATCATCC | 7874 |
rs767661610 | snp | A/T | 3.35706e-05 | 0.00409685 | intron-variant | USP7 | GRCh38.p7 | 16:8910873 | CTAAAGCTTCATTTA[A/T]AATGTAGCCAACACA | 7874 |
rs767672030 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8954703 | ATTGCAGGCCGGGCA[C/T]GGTGGACTCACACCT | 7874 |
rs767676386 | in-del | -/TGTTTT | 1.74008e-05 | 0.0029496 | intron-variant | USP7 | GRCh38.p7 | 16:8902371 | AGATACGCTATTAAC[-/TGTTTT]AATATTTACTGTTTT | 7874 |
rs767753158 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8897178 | GAAGAGAGGAGAAAG[C/T]TGCATCATTGTTCTC | 7874 |
rs767754018 | snp | A/G | 1.65501e-05 | 0.00287659 | intron-variant | USP7 | GRCh38.p7 | 16:8903264 | CCACGGGACCGGTAC[A/G]CACCATGGTCTGAGA | 7874 |
rs767759915 | in-del | -/TGTCT | 1.64864e-05 | 0.00287105 | intron-variant | USP7 | GRCh38.p7 | 16:8923207 | CCAGTAATGAAATAC[-/TGTCT]TACGTGGAATCAGAT | 7874 |
rs767759945 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8965426 | GGCGCATGCCTGTAA[A/T]CCCAGCTACTCAGGA | 7874 |
rs767781987 | snp | C/G | 0.000129196 | 0.00803625 | intron-variant, missense | USP7 | GRCh38.p7 | 16:8894522 | GTCTGAAACCCACAC[C/G]AGCCCCCGGGGGGGG | 7874 |
rs767784377 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937830 | ACACAGAAGCCAGGA[C/G]ACAACTGGACAAGAG | 7874 |
rs767799342 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8931612 | TAAATGCTTGGGCTG[A/C]AAAACACATATAACT | 7874 |
rs767803740 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961563 | TTTCCCAAAGATACA[A/G]GTCTGTAACACACAT | 7874 |
rs767841637 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8907481 | CTGGTGCTCAAACTA[A/G]TCAGGATAAAAATAC | 7874 |
rs767887299 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8903777 | AAGGCTGAGGCAGGA[G/T]AATCACTTGAATCCA | 7874 |
rs767969936 | in-del | -/AATC | | | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8965001 | TCAACTTTTCCAGTT[-/AATC]AAGGCAGTGTGGGTC | 7874 |
rs768021471 | snp | C/T | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894101 | CGAGGATGAGACATA[C/T]TACCTGGTGGGGATG | 7874 |
rs768025385 | snp | C/G/T | 1.83478e-05 | 0.00302879 | utr-variant-5-prime, intron-variant | USP7 | GRCh38.p7 | 16:8936697 | TGCATAGAATCTCTA[C/G/T]GAGCTCTACCTCAGC | 7874 |
rs768031178 | snp | A/C | 1.90751e-05 | 0.00308823 | intron-variant | USP7 | GRCh38.p7 | 16:8906593 | CAAACCTATTAGAAA[A/C]CATTTTAAAAGAAAT | 7874 |
rs768033800 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8914019 | CTGAAATTACAGGCA[A/T]GAGCGACCACACCCA | 7874 |
rs768057432 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8943431 | CGCACGGCCGGAACC[A/G]AGCTGCACAGATGCA | 7874 |
rs768067464 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8913494 | CTCAGAAATGAGGCG[A/G]GCAAGAAGACGGTAG | 7874 |
rs768076282 | in-del | -/GCGGCCTGGGCCTCGCCT | 0.000212157 | 0.0102972 | utr-variant-5-prime, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8963292 | TGGTTCATGTCGGCC[-/GCGGCCTGGGCCTCGCCT]GCGGCCTGGGCCTCG | 7874 |
rs768101406 | snp | A/C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8898126 | CAGTGGGACCCAGAA[A/C/G]GGAAGGGTTGGCTGC | 7874 |
rs768120894 | snp | A/G | 1.66913e-05 | 0.00288883 | intron-variant | USP7 | GRCh38.p7 | 16:8906398 | CTTTCTGATGAGCTT[A/G]CATTCAGCCCTGGGT | 7874 |
rs768121451 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8945514 | CCAACAGACACCTTG[A/T]ACATTTCTGTGCACT | 7874 |
rs768178650 | in-del | -/TT | 1.66131e-05 | 0.00288206 | intron-variant | USP7 | GRCh38.p7 | 16:8899215 | AAAGGAAGGTTCACA[-/TT]TTGGGGAAAAATTGA | 7874 |
rs768196031 | snp | A/G | 1.73225e-05 | 0.00294295 | intron-variant | USP7 | GRCh38.p7 | 16:8917000 | AAGAGGAAGCAGAAT[A/G]GCAAAGGCAGATGTC | 7874 |
rs768246876 | in-del | -/AA | 1.67866e-05 | 0.00289707 | intron-variant | USP7 | GRCh38.p7 | 16:8903427 | TGTATGAAAGCACAG[-/AA]AAGACTTGACAACTG | 7874 |
rs768254284 | snp | C/G | 1.64958e-05 | 0.00287187 | missense, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8930341 | CATCACTCAGGGCCA[C/G]ATTCCCATTGATCAC | 7874 |
rs768266041 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8954844 | GGGCGCCTGTAGTCC[C/T]AGCTACTCAGGAGGC | 7874 |
rs768285317 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893272 | ATGAACTGTTGAGAT[C/T]GTAAGTCTGCCAAGG | 7874 |
rs768316380 | snp | C/T | 0.000115533 | 0.00759957 | intron-variant | USP7 | GRCh38.p7 | 16:8899072 | TGTTTCAATGAACTG[C/T]GGAAAGCATGCAGTC | 7874 |
rs768343533 | snp | A/G | 1.69648e-05 | 0.00291241 | intron-variant | USP7 | GRCh38.p7 | 16:8900495 | AAAATCCTGAAATTA[A/G]TACAAAGTGATACAA | 7874 |
rs768357840 | snp | A/G | 3.29609e-05 | 0.00405948 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8903305 | ACAAACTCAGCAAGC[A/G]AGGAGTTCTTCAATA | 7874 |
rs768359877 | snp | A/G | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8899739 | GGGTAATTCACTGTT[A/G]TCATTTTCAGGGTCA | 7874 |
rs768365905 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8939964 | TTAGCCAAGCATGGT[A/G]GCACATGCCTGTAAT | 7874 |
rs768404148 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8902136 | CCAGCTCGGGATCAA[C/T]TGTTTCCAGGAATAT | 7874 |
rs768409314 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8911649 | TACAGGCTGCAGCCC[A/G]GAGAAGGCAAACCCA | 7874 |
rs768421982 | snp | A/C | | | missense, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8930305 | TACCATCCTCCATGT[A/C]CTCCTCCGCGGTGTT | 7874 |
rs768430547 | snp | C/T | 1.65168e-05 | 0.00287369 | intron-variant | USP7 | GRCh38.p7 | 16:8896961 | GTTAACTGCCACCCC[C/T]AACTGAACGTCCACA | 7874 |
rs768445664 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8926681 | CCAAGTATGCTAGGT[A/T]TTAGCAAGGACACCC | 7874 |
rs768474566 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964717 | GGTTCGCTTGGGAGG[C/T]TGACTGAGGCTGCAG | 7874 |
rs768477107 | snp | A/G | 1.80143e-05 | 0.00300114 | intron-variant | USP7 | GRCh38.p7 | 16:8902335 | GTGCAGAGGACTAAC[A/G]CCTTCTGCACGGTTC | 7874 |
rs768501133 | in-del | -/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8896139 | CCACCATGCCCAGCT[-/T]TTTTTTTTTTTTTTT | 7874 |
rs768506460 | in-del | -/TGACTT | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8936853 | AACTCTGAAAGAATC[-/TGACTT]TGGTTAACAACATAC | 7874 |
rs768523700 | snp | C/G | 1.6483e-05 | 0.00287076 | intron-variant | USP7 | GRCh38.p7 | 16:8905360 | AACACACACCAGCAG[C/G]GATCAAGCACTGTGA | 7874 |
rs768595730 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894034 | CTTTTCAAGGTAAGT[A/G]TAGCGACTCCTCTTT | 7874 |
rs768764601 | snp | C/G | | | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8901043 | CTCTGTCACACATAA[C/G]TGGGAGCAAGTCACC | 7874 |
rs768774774 | snp | A/T | 6.38957e-05 | 0.00565188 | utr-variant-5-prime, intron-variant | USP7 | GRCh38.p7 | 16:8936621 | CCAGCCATCTCTGCA[A/T]GGCTCTGCAGTGGCC | 7874 |
rs768827892 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8955946 | TGAATGGGGTGGCAA[C/G]AGAGACAGCCAGATG | 7874 |
rs768840851 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8936990 | CAGGCGCTCTGTCAT[A/C]ATTTTGCAACTTTTC | 7874 |
rs768851134 | snp | A/G | 1.65272e-05 | 0.0028746 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8901017 | AAGGCTAGTATCTTG[A/G]ATAAATCCTGCTCTG | 7874 |
rs768864444 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8934242 | AAGTGTAAGCAGTCT[A/G]AAGTGTGGAAAATAA | 7874 |
rs768865469 | snp | A/T | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8904521 | GTAATCGCTCCACCA[A/T]CTGCTGAGGAATATC | 7874 |
rs768871695 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8942816 | GCCTCCAAAAGTGTT[A/G]GGGTTACAGACATGA | 7874 |
rs768875596 | snp | C/T | 4.94523e-05 | 0.00497229 | intron-variant | USP7 | GRCh38.p7 | 16:8895160 | GATTTCCTGGGGACA[C/T]GGACAACAGACACAG | 7874 |
rs768881468 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8894884 | GGACATGTGCTCACA[C/T]AGTCACTCCCAGCAC | 7874 |
rs768917575 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957397 | CTCCAGGATAAAACT[C/T]CTTTGCCTTGGAAAT | 7874 |
rs768925488 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8905902 | TCACTGTTCTCTCGT[C/G]CTGTCGGGTCCCTCC | 7874 |
rs768952361 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8933246 | CCCAGCTCCCAATAG[A/G]ATGTTAAAAAAATTT | 7874 |
rs768959512 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8951872 | TGCGTTATTTTGCTT[A/C]ATCTCTTTTTATGCC | 7874 |
rs768998403 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8906980 | GACTTAGTTTTAACT[A/G]GCTCTACAAATTTTG | 7874 |
rs769013107 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8916156 | ACTGGAGTAACAACA[G/T]AAGTCACCACTGTAC | 7874 |
rs769020407 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8948661 | TTCTGCGAGAAAAGG[G/T]AACGACTACTGGCTA | 7874 |
rs769074623 | snp | C/T | 1.67158e-05 | 0.00289096 | intron-variant | USP7 | GRCh38.p7 | 16:8920330 | CACAAAAGACATTTT[C/T]AACAGCACCTGATTA | 7874 |
rs769076526 | in-del | -/AC | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950342 | AGTGCTCTCTGATAA[-/AC]ACTCAAGATTAAAAC | 7874 |
rs769080231 | snp | C/T | 0.000264345 | 0.0114936 | intron-variant | USP7 | GRCh38.p7 | 16:8898506 | TCTCTTTATGACCCA[C/T]AGTTACATTAATTTG | 7874 |
rs769090955 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957479 | CTGGGTGAGGTGGCT[C/G]ACACCTATAATCCCA | 7874 |
rs769106480 | snp | C/T | 1.66835e-05 | 0.00288816 | intron-variant | USP7 | GRCh38.p7 | 16:8910697 | TAAAAGAATTGAAAA[C/T]AAAGAAGAACGCTAC | 7874 |
rs769110078 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8948068 | ACTGCATGCCCTGCA[A/G]ACGTCAGTCAGCTCC | 7874 |
rs769112464 | snp | A/G | 1.65457e-05 | 0.00287621 | intron-variant | USP7 | GRCh38.p7 | 16:8898448 | TTAAGCTATTAAGAA[A/G]AGAAAGATTCACATC | 7874 |
rs769117620 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8903605 | AGGCTGTGGGCAGGG[C/T]ACGGTGGCTCATGCA | 7874 |
rs769153331 | snp | G/T | 6.36868e-05 | 0.00564264 | utr-variant-5-prime, intron-variant | USP7 | GRCh38.p7 | 16:8936718 | CTACCTCAGCATTCT[G/T]TTTTATTTTTTAAAG | 7874 |
rs769164213 | in-del | -/AAGTC | 9.96852e-05 | 0.00705922 | intron-variant | USP7 | GRCh38.p7 | 16:8910848 | AAGAGAGAGAGAGAA[-/AAGTC]AAGTGCTAAAGCTTC | 7874 |
rs769192378 | snp | G/T | 6.69031e-05 | 0.00578334 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8920440 | CCTTTCTCAGGATCG[G/T]TCACTTCCTATAAAA | 7874 |
rs769207546 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8913824 | GGCACAATCATGGCT[C/T]GCTGCAGACTTAAAC | 7874 |
rs769280580 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8914878 | GAGCTATGGTTGCAC[C/T]CCAGCCTGTACAGCA | 7874 |
rs769287084 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8955564 | ACAAAAAATTAGCCG[C/G]GCATGGCGGCGCGCC | 7874 |
rs769315876 | snp | C/T | 1.66726e-05 | 0.00288722 | intron-variant | USP7 | GRCh38.p7 | 16:8917186 | AAATAAGAATTTTTA[C/T]TCTGAGAAGATGCAG | 7874 |
rs769338393 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8899040 | TGGCGAGCTAATTAT[C/T]AAAATTAGTTCCAAG | 7874 |
rs769348748 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8924899 | GAACTTTGGAAGGAA[A/G]AGCAGCTGAAAGAGG | 7874 |
rs769382825 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8919055 | CTGATTCGTGAAAAA[C/T]AACGTCTGTAGCAGG | 7874 |
rs769402609 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8922550 | GGGGAACATGTTACT[A/G]AGGGTTCCAAAGGGC | 7874 |
rs769411234 | in-del | -/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8910211 | ACCAGCAGCCAGAAA[-/C]CAGCCCATTTCCCTT | 7874 |
rs769414495 | snp | C/T | 1.80354e-05 | 0.00300289 | intron-variant, synonymous-codon | USP7 | GRCh38.p7 | 16:8894500 | GCCCCAGACCACTTG[C/T]TTCTTAGTCTGAAAC | 7874 |
rs769419856 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8920001 | CCCTTCCTCACACTC[A/G]GAGAGGACTTCCTCC | 7874 |
rs769442923 | snp | C/T | 1.65151e-05 | 0.00287355 | intron-variant | USP7 | GRCh38.p7 | 16:8896969 | CCACCCCTAACTGAA[C/T]GTCCACAATTGGGCT | 7874 |
rs769446474 | snp | C/T | 1.64732e-05 | 0.0028699 | intron-variant | USP7 | GRCh38.p7 | 16:8895018 | AGCCACTCGGCCAAC[C/T]ACAACAGCATACCTG | 7874 |
rs769490424 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8932071 | TCACCTCCCCCTCCA[A/G]GAACTCTCCAAAACC | 7874 |
rs769548577 | snp | C/T | 1.65688e-05 | 0.00287821 | intron-variant | USP7 | GRCh38.p7 | 16:8899575 | TTCTGGAGTGGGATC[C/T]GAAGAGGAAAGGAGC | 7874 |
rs769574241 | snp | C/G | 1.65187e-05 | 0.00287386 | missense, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8930363 | ATTGATCACAGGGTT[C/G]TGAGTAATTCTTGGT | 7874 |
rs769609900 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8919539 | TTTCTGTAGACACAC[A/G]CACAAGAAGAAACAG | 7874 |
rs769634736 | snp | A/T | 1.65542e-05 | 0.00287695 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8899177 | GAGCCTCTGTGCAAC[A/T]GTCTTTGCAACCTAA | 7874 |
rs769648852 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961147 | AAGTAGCCTTGAAAA[C/T]GTGCATGGAGACTGA | 7874 |
rs769700501 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8926551 | TAGCTTTCACAGATA[C/G]GGCCAGCCAGATTGT | 7874 |
rs769729147 | in-del | -/G | 1.6621e-05 | 0.00288274 | intron-variant | USP7 | GRCh38.p7 | 16:8904424 | GAGTCCCAGAAGGGC[-/G]GGGGGCTGACCTGCA | 7874 |
rs769729723 | snp | C/T | 1.65209e-05 | 0.00287405 | intron-variant | USP7 | GRCh38.p7 | 16:8898515 | GACCCATAGTTACAT[C/T]AATTTGGACTCATAC | 7874 |
rs769742440 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8959900 | GCAGTCTAAGTGTCA[C/T]AGAAAAGTCTAACAT | 7874 |
rs769751516 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8928222 | TAAGAAGTCTTCTGT[A/G]CAAATCAGTCAAGTC | 7874 |
rs769755718 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8904743 | GTCAGGAAATCAAGA[A/C]CATCTTGGCTAACAT | 7874 |
rs769761004 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8923265 | TCCTACGCTTTTTTG[A/G]TGTGGTCTGTCTGGA | 7874 |
rs769776155 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8904828 | ATACAAAAAATTAGC[C/G]AGGCGTGGTGGCAGA | 7874 |
rs769796432 | snp | A/G | 1.65056e-05 | 0.00287272 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8906494 | CTCCACTATGAACCA[A/G]GACTGCATGAAGAAT | 7874 |
rs769900956 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8948265 | TCAGCTCACTGCAGC[A/C]TCAACTTCCTGGGCT | 7874 |
rs769909734 | snp | A/G | 1.69772e-05 | 0.00291347 | intron-variant | USP7 | GRCh38.p7 | 16:8920452 | TCGGTCACTTCCTAT[A/G]AAACATAAATAAGAA | 7874 |
rs769922580 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937241 | ATTAACACGAAACAA[C/T]GTGTATAAGACAAGC | 7874 |
rs769964073 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8919286 | CAATGGTCACCGATT[C/G]CCTTCTGCTTGCTCC | 7874 |
rs769974523 | snp | A/G | 3.30584e-05 | 0.00406548 | intron-variant | USP7 | GRCh38.p7 | 16:8898455 | ATTAAGAAAAGAAAG[A/G]TTCACATCAGATACC | 7874 |
rs770001568 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8901968 | AGCTTTTGTGGAATT[C/G]ATCAACACATCTTTC | 7874 |
rs770022127 | in-del | -/ATCT | | | intron-variant | USP7 | GRCh38.p7 | 16:8949229 | AAAGCACAGATGCAA[-/ATCT]ATCTAATCCTTTACA | 7874 |
rs770031572 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8934914 | AAATGAGTTAGTTCC[A/G]CAAGAGGATTAAAAT | 7874 |
rs770036561 | snp | A/G | 6.81118e-05 | 0.00583534 | intron-variant | USP7 | GRCh38.p7 | 16:8903451 | GACAACTGACAAAAA[A/G]TGAGTCCACACTGAA | 7874 |
rs770070914 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957532 | GAGGATTGCTTGAGA[C/T]CAGGAATTCCACACC | 7874 |
rs770071063 | snp | C/G | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8905209 | TGATTCCCTGATGTA[C/G]ACTAACATGTAAGCA | 7874 |
rs770071588 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8943740 | AATATGTATTAAAAT[A/C]AAAATGTTGAATGTC | 7874 |
rs770076868 | snp | A/G | 1.64808e-05 | 0.00287057 | intron-variant | USP7 | GRCh38.p7 | 16:8901120 | AAAATCTACTCAGAA[A/G]GTAAGTGCACGAAGG | 7874 |
rs770099597 | in-del | -/A | 6.0443e-05 | 0.00549708 | frameshift-variant, utr-variant-5-prime, intron-variant | USP7 | GRCh38.p7 | 16:8936592 | CTCACCTTCCAGCCC[-/A]AAGCCTGTGGTTCCC | 7874 |
rs770137523 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8965102 | AAGGCCAGAAGATTG[C/T]GGTACCTGTCTTCTC | 7874 |
rs770151220 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8931399 | CACCATGTCGGTCAA[C/G]TGGTCTCGAACTCCT | 7874 |
rs770155611 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8940028 | GCTTGAACCAGGGAG[C/G]CGAAGGTTGTAGTGA | 7874 |
rs770161637 | snp | A/G | 3.29538e-05 | 0.00405904 | intron-variant | USP7 | GRCh38.p7 | 16:8894746 | GCAAGGCTTGAGCCT[A/G]TGGCCCGCCAAGCCC | 7874 |
rs770172836 | snp | A/G | 6.75174e-05 | 0.00580983 | intron-variant | USP7 | GRCh38.p7 | 16:8900502 | TGAAATTAGTACAAA[A/G]TGATACAATCCTTCA | 7874 |
rs770197339 | snp | A/G | 4.94238e-05 | 0.00497086 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8894853 | TTCTCGAAAATGCTC[A/G]CCCTAGAATGGCAAA | 7874 |
rs770230956 | snp | A/G | 1.66499e-05 | 0.00288525 | intron-variant | USP7 | GRCh38.p7 | 16:8910855 | AGAGAGAAAAGTCAA[A/G]TGCTAAAGCTTCATT | 7874 |
rs770264553 | snp | C/T | 1.64811e-05 | 0.00287059 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8903335 | ACTTTGAACACAGTG[C/T]ATTTCACTTTTTCTT | 7874 |
rs770314625 | snp | C/G | 1.65704e-05 | 0.00287836 | intron-variant | USP7 | GRCh38.p7 | 16:8921116 | AGGGAACAACAAGCA[C/G]TAATGCACCAATTGT | 7874 |
rs770315423 | in-del | -/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8895416 | GAAATGTCAACAGCT[-/C]TAAATTCAAGTGATC | 7874 |
rs770318982 | snp | A/G | 1.64901e-05 | 0.00287137 | intron-variant | USP7 | GRCh38.p7 | 16:8910721 | ACGCTACAACAGGAC[A/G]CTAGCACAAAACACT | 7874 |
rs770392977 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8904964 | GCAAGAGCAAGACTC[C/T]GTCTCAAAAAAATAA | 7874 |
rs770417325 | snp | A/C/T | 3.55027e-05 | 0.00421311 | intron-variant | USP7 | GRCh38.p7 | 16:8902362 | GTTCCAAACCAGATA[A/C/T]GCTATTAACAATATT | 7874 |
rs770418473 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8907246 | GTCTGCCACTGGCTC[A/C]AACAAAAATAAAAAC | 7874 |
rs770435953 | snp | A/G | 1.65427e-05 | 0.00287595 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8906530 | TTGCAGGGTCCTTAG[A/G]ATCTGTTTTTTGCAA | 7874 |
rs770437948 | snp | A/C/T | 4.94395e-05 | 0.00497169 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8897088 | ATGCTTGTCTGGATA[A/C/T]AGTGTTATTTCCTAA | 7874 |
rs770443951 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8946898 | CATTTAGCAGACCTG[C/T]AAAACTTGATGAATC | 7874 |
rs770448781 | snp | A/G | 1.93913e-05 | 0.00311372 | intron-variant | USP7 | GRCh38.p7 | 16:8902500 | GAAAAAAATATTAAG[A/G]GTAGATTAAAATAAA | 7874 |
rs770536551 | snp | C/G/T | 4.9999e-05 | 0.00499974 | intron-variant | USP7 | GRCh38.p7 | 16:8908301 | CCCCCTAGACCAGCA[C/G/T]GATGATGAAATCTTA | 7874 |
rs770546756 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8946420 | ACCGCATCTCTAAAT[-/A]AAGAAAAAAACTGTT | 7874 |
rs770562003 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8914971 | GTTCTATTTAAACAG[A/T]CACCTAAAACATGCA | 7874 |
rs770565789 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938606 | AGTCCCAGCTACTCC[A/G]GAGGCTGAGGCAGGA | 7874 |
rs770595131 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893831 | TCAAAAAGGGCAGTC[-/A]AATAGATACAGAGAA | 7874 |
rs770650286 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8920955 | CCTTTGAATGTCTGA[C/T]TAAAAAGTGAGACGT | 7874 |
rs770653423 | snp | G/T | 1.65201e-05 | 0.00287398 | intron-variant | USP7 | GRCh38.p7 | 16:8919185 | TTGCAGATACCCCAT[G/T]GCTCCTGCAGTGTGT | 7874 |
rs770661050 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8946206 | CTGTAAGAAAACACA[A/G]GAAAACATCTGTCAT | 7874 |
rs770675054 | snp | C/T | 1.65059e-05 | 0.00287275 | intron-variant | USP7 | GRCh38.p7 | 16:8916479 | TCATTGTAAGAAATA[C/T]ACAAGTATTGCTTGA | 7874 |
rs770706913 | snp | C/T | 4.95258e-05 | 0.00497599 | intron-variant | USP7 | GRCh38.p7 | 16:8895603 | AGCAGATGGGGCTCA[C/T]GAATTCTCTCTGGTG | 7874 |
rs770709377 | in-del | -/AACAA | 6.59299e-05 | 0.00574113 | intron-variant | USP7 | GRCh38.p7 | 16:8905165 | CACAGTAAAGAACAG[-/AACAA]AAGTGAACACTACTC | 7874 |
rs770721553 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8943120 | ACCAAGCCCCAAAGA[A/G]GGCCACATATAATAT | 7874 |
rs770725411 | snp | A/G | 3.29478e-05 | 0.00405867 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8899697 | ATCAACGCGGTGGTA[A/G]AGATCTCGGAAATAC | 7874 |
rs770725481 | snp | A/C | 1.64876e-05 | 0.00287116 | intron-variant | USP7 | GRCh38.p7 | 16:8895173 | CACGGACAACAGACA[A/C]AGTTCTGTAAGTGCA | 7874 |
rs770727777 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8953081 | ACCTCGTAATCTGTC[A/G]CCTTGGCCTCCCGAA | 7874 |
rs770735072 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8919088 | GTTCATGTAACAAGT[C/T]GCTCCCTGATTCTTT | 7874 |
rs770756666 | snp | A/G | 1.7653e-05 | 0.00297089 | intron-variant | USP7 | GRCh38.p7 | 16:8923425 | GTGTCTGCAAAAAAA[A/G]CACATCATCAGTCAC | 7874 |
rs770781522 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8910833 | GATTCAAATACTTTA[A/G]AGAGAGAGAGAGAAA | 7874 |
rs770813213 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8952222 | GCCACTGAATTCCAG[C/G]CTGGGCACGAGGGAG | 7874 |
rs770819293 | in-del | -/A | 1.67198e-05 | 0.0028913 | intron-variant | USP7 | GRCh38.p7 | 16:8920333 | AAAGACATTTTTAAC[-/A]AGCACCTGATTAAAG | 7874 |
rs770854528 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8908269 | AATATAAAGACTGAG[A/G]AAAGCACTGAGACTA | 7874 |
rs770860921 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8919303 | CTTCTGCTTGCTCCA[C/G]TGTGTGAACTGGTGC | 7874 |
rs770891854 | snp | G/T | 1.64784e-05 | 0.00287035 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8915490 | GGTGCCCTCTACACA[G/T]GTGCCTTTCATCTTA | 7874 |
rs770901431 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950771 | ACCCAAGGGTCACCT[A/G]GCTTACATGCATGTC | 7874 |
rs770902494 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8923289 | GTCTGGATAAAAGCG[C/T]GGCATCACCATAATC | 7874 |
rs770910286 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8895204 | AGTGATGTGGTCAAA[A/G]TGTCCACATCTCAAT | 7874 |
rs770947527 | snp | A/G | | | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962432 | ATACCTCAAACTACA[A/G]TGCCTTGGAAAATTA | 7874 |
rs770958985 | snp | A/G | 1.66048e-05 | 0.00288134 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8921267 | AATTTATTATCTTCA[A/G]CACTGCTTGTGCATG | 7874 |
rs770960061 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8929858 | AATCTGATTTCATCC[C/T]TAACAGGAGCGGGGA | 7874 |
rs771034365 | snp | A/T | 1.66799e-05 | 0.00288785 | intron-variant | USP7 | GRCh38.p7 | 16:8910859 | AGAAAAGTCAAGTGC[A/T]AAAGCTTCATTTATA | 7874 |
rs771064279 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8908273 | TAAAGACTGAGGAAA[A/G]CACTGAGACTAACCC | 7874 |
rs771079293 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8951239 | GCCTATGAAGATGTA[C/T]ATCATATATATATTT | 7874 |
rs771088307 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893207 | AAAGGCTTTCTTGTC[G/T]TCTGTTCCACTTTAA | 7874 |
rs771103070 | in-del | -/CTG | 0.0110893 | 0.0736319 | cds-indel, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8963255 | CTGCTCGCCCGCTTT[-/CTG]CTGCTGCTGCTGCTG | 7874 |
rs771109724 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8926586 | CTACGAGGAATTACA[C/T]GAGACTCAGTGATGG | 7874 |
rs771116444 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8925745 | GCCTCACACTCAAGG[C/T]ACATTTCTTAGAACA | 7874 |
rs771127611 | snp | A/G | 1.64746e-05 | 0.00287002 | intron-variant | USP7 | GRCh38.p7 | 16:8894870 | CCTAGAATGGCAAAG[A/G]ACATGTGCTCACACA | 7874 |
rs771143610 | snp | A/T | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8902084 | CGTGGGCACTTACGA[A/T]CTTTATCAAACTTGG | 7874 |
rs771144050 | snp | A/T | 5.65478e-05 | 0.00531702 | intron-variant | USP7 | GRCh38.p7 | 16:8898686 | CTTGTTTATTTGCCT[A/T]AAAACAAATATCTGT | 7874 |
rs771152131 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8949544 | GAAGCCTTGCCGCTG[C/T]CATCCTTACCTCCAA | 7874 |
rs771165336 | snp | G/T | 6.78351e-05 | 0.00582348 | intron-variant | USP7 | GRCh38.p7 | 16:8900970 | AATATACTAATTATG[G/T]AAAAATAAACCATCC | 7874 |
rs771166806 | in-del | -/AC | | | intron-variant | USP7 | GRCh38.p7 | 16:8935869 | ATTTGTGATGTCATA[-/AC]ACAGAACTGCTACCC | 7874 |
rs771170934 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8953268 | CTCCCCTGCACACGT[A/G]TTCAGGGCTCCTTCA | 7874 |
rs771199813 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8935961 | TAACCCCTGAGATAA[C/T]AGATCAGAATAAGCA | 7874 |
rs771224242 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8913940 | ATGGAGTCTCACTAT[A/G]TTGCCCAGGCTGGCC | 7874 |
rs771226504 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8923775 | ATGGCTCATATCTGT[G/T]CAAGGACGGGACTTC | 7874 |
rs771237858 | snp | A/G | 1.65181e-05 | 0.00287381 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8898554 | AGTAAAGTTTCTTAG[A/G]TTGTCTAGGCTTGAA | 7874 |
rs771238235 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8959526 | CACATCAGAGTGAGA[G/T]GCTAGGTTTGGCCTA | 7874 |
rs771240253 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8948832 | AGCCAGGCGTGGTGG[C/T]GTGTGCCTGCAGTTC | 7874 |
rs771260597 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8900104 | GCCCAGTCTCTGACC[A/G]TGAGTCAGGAAATCT | 7874 |
rs771261119 | in-del | -/TTTT | | | intron-variant | USP7 | GRCh38.p7 | 16:8919603 | CTAAACTCCCAGAGC[-/TTTT]TTTATTTTGTGATTT | 7874 |
rs771297015 | in-del | -/AAAATT | 1.65938e-05 | 0.00288039 | intron-variant | USP7 | GRCh38.p7 | 16:8894652 | TAAACTAAAAGAAAA[-/AAAATT]AAAACTCCTCCGTTA | 7874 |
rs771312092 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8922593 | TGGCAGGGAGACTAG[C/G]ACAGGTGCAGTCCAA | 7874 |
rs771315377 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8955591 | CGCCCCTGTAGTCCT[A/G]GCTACTTGGGAGGCT | 7874 |
rs771316844 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8932165 | ACCCAAGCATCTCAA[A/G]ACATTCAAAATACCA | 7874 |
rs771329841 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8958680 | TTTCCTGCCACTATC[C/T]AGTGTTCCACTTCCC | 7874 |
rs771341350 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8909485 | TTAATACAGTCTGAA[A/T]GATAAAAGGATTCTG | 7874 |
rs771357137 | snp | C/T | 1.67829e-05 | 0.00289675 | intron-variant | USP7 | GRCh38.p7 | 16:8904392 | ATAGAGATGGGTGCC[C/T]GGCTGCATGGTGACC | 7874 |
rs771367968 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8916713 | CATAATTCAAAGATA[A/G]ATTTACTGCTGGGGA | 7874 |
rs771384506 | snp | A/G/T | 3.37196e-05 | 0.00410595 | intron-variant | USP7 | GRCh38.p7 | 16:8900650 | AGTGAAAGATATAAA[A/G/T]TTGTTACACTGCAAG | 7874 |
rs771410773 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8940801 | CCTGGAATATTAGCC[A/G]GACATGGTGGCGCAC | 7874 |
rs771447115 | snp | A/G | 3.31214e-05 | 0.00406935 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8915255 | CACACAACACTTACT[A/G]TTTTTCTTTCCTTTG | 7874 |
rs771453890 | in-del | -/ACTCCG | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938161 | GCAAACAGGCACGAC[-/ACTCCG]AGAAGGCTGAAGTTC | 7874 |
rs771458687 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8899268 | CTTAATTACTTAAAA[C/T]GTGCCATGAGCAGCC | 7874 |
rs771468894 | snp | G/T | 5.56323e-05 | 0.00527381 | intron-variant | USP7 | GRCh38.p7 | 16:8930426 | AAAGAAATTCCACGG[G/T]TTTTACATTCATGGC | 7874 |
rs771474145 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8952246 | GAGGGAGAGCCTGTC[G/T]CCAAAAAAATATTAA | 7874 |
rs771520596 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8896558 | TCTACAGCCCAAATG[A/T]TGGCTAGATGGAACA | 7874 |
rs771556702 | snp | C/T | 1.6531e-05 | 0.00287493 | missense, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8930371 | CAGGGTTCTGAGTAA[C/T]TCTTGGTGGGTCATC | 7874 |
rs771576964 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8899718 | TCGGAAATACTCCTT[C/T]GCGGTGGGTAATTCA | 7874 |
rs771580473 | snp | C/T | 1.65614e-05 | 0.00287757 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8894629 | GCCCATCATTACAAT[C/T]GCAAATTTAAACTAA | 7874 |
rs771601034 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8939432 | TTTGACCATTCACTT[A/G]CTGACATCTGGGTCC | 7874 |
rs771608324 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8895336 | GAAGATATCCAAGTT[A/T]CTTCCCCCTCCCCCA | 7874 |
rs771610275 | snp | A/G | 1.64743e-05 | 0.00287 | intron-variant | USP7 | GRCh38.p7 | 16:8895000 | GCTCCAGGTTTTGAC[A/G]TGAGCCACTCGGCCA | 7874 |
rs771713030 | snp | G/T | 0.000202737 | 0.0100661 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962495 | CGAGTCAGGTTTGAT[G/T]CTGATGCAGGCAGCC | 7874 |
rs771732431 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8929086 | GGAAATGTTGGAACA[C/G]ATTGCTCTGTGGGAA | 7874 |
rs771763587 | snp | C/G | 1.67329e-05 | 0.00289243 | intron-variant | USP7 | GRCh38.p7 | 16:8903230 | GAAGGTGGACGTTGG[C/G]AGCCACGGTGGGGTA | 7874 |
rs771770410 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8945197 | CCACTGCACTCCAGC[C/T]TGGGCAACAAGAGCG | 7874 |
rs771779959 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8947807 | CTGCCTGATGGGTTT[C/G]TGCCATGCTGCCTCA | 7874 |
rs771781901 | snp | A/T | 3.55442e-05 | 0.00421555 | intron-variant | USP7 | GRCh38.p7 | 16:8908496 | TTAGCCTCTACTTAC[A/T]CCTGGAAGCAATGAA | 7874 |
rs771783810 | snp | A/C/T | 0.000100462 | 0.00708675 | intron-variant | USP7 | GRCh38.p7 | 16:8902508 | TATTAAGAGTAGATT[A/C/T]AAATAAAAACACGCT | 7874 |
rs771812448 | in-del | -/AT | 9.90238e-05 | 0.00703577 | intron-variant | USP7 | GRCh38.p7 | 16:8899110 | AGCAAGTGTCCACAC[-/AT]GTGACCTACCCTTGA | 7874 |
rs771825799 | snp | A/G | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8905228 | AACATGTAAGCATTA[A/G]TGCAGTGTCGAACAG | 7874 |
rs771835747 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8940530 | GGCAACCCAGGGCGG[A/G]AGGTGGGGCAGTTAC | 7874 |
rs771837381 | snp | A/T | 1.64751e-05 | 0.00287007 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893991 | CTTGAACACACCAGC[A/T]TGGAAATCAGTTATG | 7874 |
rs771857838 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8935063 | TCTTTTATTGTTCAA[C/G]ACAGATGTACAACAT | 7874 |
rs771871815 | snp | C/G | 1.6593e-05 | 0.00288031 | intron-variant | USP7 | GRCh38.p7 | 16:8908313 | GCATGATGATGAAAT[C/G]TTAACTTTATATCCC | 7874 |
rs771872079 | snp | A/T | 1.64874e-05 | 0.00287113 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893950 | AGTTCTAGGCTGTTA[A/T]GGGGCCACCCACACA | 7874 |
rs771877206 | snp | A/C | 1.64779e-05 | 0.00287031 | intron-variant | USP7 | GRCh38.p7 | 16:8905345 | CACTGCAAGGAAAAC[A/C]ACACACACCAGCAGC | 7874 |
rs771949960 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8943817 | AAATGAGCATTCACG[A/C]TGGGGGATAAACACA | 7874 |
rs771965900 | snp | C/T | 6.76098e-05 | 0.00581381 | intron-variant | USP7 | GRCh38.p7 | 16:8901279 | GATCCAAACACTCAG[C/T]ACAATGCTTAAAAAA | 7874 |
rs771980803 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8910480 | ACACCAGTAAGGTGA[A/G]GAACGGGGAAAGGAC | 7874 |
rs772018844 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8912359 | CAGGAGGCTGAAAGG[A/T]GAATTGCTTGAACCC | 7874 |
rs772073760 | snp | A/G | 1.64977e-05 | 0.00287203 | intron-variant | USP7 | GRCh38.p7 | 16:8916486 | AAGAAATATACAAGT[A/G]TTGCTTGAAACTTAC | 7874 |
rs772106816 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8921866 | CAAAAACCATACATA[C/T]AGCACTTAAGCCAAA | 7874 |
rs772113416 | snp | C/T | 1.68786e-05 | 0.002905 | intron-variant | USP7 | GRCh38.p7 | 16:8900652 | TGAAAGATATAAAAT[C/T]GTTACACTGCAAGTT | 7874 |
rs772130641 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8899837 | GGCATCATCTTTTAC[A/T]CAACAGTGACACCAA | 7874 |
rs772193545 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8923529 | CTGCTAAAACCTAAC[-/A]GTTTGAAAAAATTGC | 7874 |
rs772218765 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8909605 | TCAACAGACCAGAAT[A/G]TTTCTTCATCACACC | 7874 |
rs772226067 | snp | A/C | | | intron-variant, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8949615 | ACAACACCACCTCTT[A/C]ACCATGCCTTCCTTC | 7874 |
rs772256210 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8919490 | CTTATCACACGCAAG[A/G]TCAGCACAACGTGGA | 7874 |
rs772259782 | snp | C/G/T | 3.345e-05 | 0.00408951 | intron-variant | USP7 | GRCh38.p7 | 16:8904404 | GCCCGGCTGCATGGT[C/G/T]ACCCGGAGTCCCAGA | 7874 |
rs772263748 | in-del | -/CAG | | | intron-variant | USP7 | GRCh38.p7 | 16:8953384 | AATGAAAGCCTACAC[-/CAG]CAGCCTCTGTGGACA | 7874 |
rs772300332 | snp | C/T | 1.65452e-05 | 0.00287616 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8899165 | TGGATCTGTGTTGAG[C/T]CTCTGTGCAACTGTC | 7874 |
rs772315765 | in-del | -/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8936536 | CAGTATTGGTTATCT[-/C]CCATCCATCACCAGC | 7874 |
rs772357083 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8915115 | ACAAGCCTGTGTTCA[A/C]CCAGTGAGCTGTTTG | 7874 |
rs772362472 | snp | A/T | 1.64814e-05 | 0.00287061 | intron-variant | USP7 | GRCh38.p7 | 16:8923212 | AATGAAATACTGTCT[A/T]ACGTGGAATCAGATT | 7874 |
rs772372409 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8940884 | AGTGTCCAGAACCTG[A/G]AATATATACAGTCTC | 7874 |
rs772380599 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961045 | CCAATTTGAGATTCT[A/G]CTAAATTTACAGATT | 7874 |
rs772392719 | in-del | -/CTGGAGA | | | intron-variant | USP7 | GRCh38.p7 | 16:8908544 | AAGATTGGAACATGT[-/CTGGAGA]CTCTGGAGACAAAGG | 7874 |
rs772398924 | snp | G/T | 1.6534e-05 | 0.00287519 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8898417 | TCGCCTGTTCTCAAA[G/T]TCTGTGATTTTCATC | 7874 |
rs772428972 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8916089 | GGGAGAGTAATCACC[A/G]CATGCTGAGGTCTGC | 7874 |
rs772448433 | snp | A/G | 1.64751e-05 | 0.00287007 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8919109 | CTGATTCTTTAAGCC[A/G]ACGTAGCCTGTGTGC | 7874 |
rs772475725 | snp | A/G | | | intron-variant, missense | USP7 | GRCh38.p7 | 16:8894538 | AGCCCCCGGGGGGGG[A/G]AGAACCCTTACCGGG | 7874 |
rs772476369 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8916899 | CTGACACGATTAAAT[C/G]CTCAAGCCTCCCTAA | 7874 |
rs772486366 | snp | C/G | 6.59533e-05 | 0.00574215 | intron-variant | USP7 | GRCh38.p7 | 16:8901096 | ATGTGTAGCTGTAAT[C/G]TACTGAGCAAAATCT | 7874 |
rs772528808 | snp | A/C | 1.67818e-05 | 0.00289665 | intron-variant | USP7 | GRCh38.p7 | 16:8920312 | AAGCTTCTTTCACTG[A/C]AGCACAAAAGACATT | 7874 |
rs772621112 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8955938 | AAGTACTGTGAATGG[C/G]GTGGCAAGAGAGACA | 7874 |
rs772666129 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8960051 | ATTCAATAGCGTCTA[C/G]ACCGACCATCTGAGT | 7874 |
rs772674228 | snp | C/G | 1.64789e-05 | 0.0028704 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8902176 | GTTTTCATTATCACT[C/G]AGCTCAATCATCTAT | 7874 |
rs772751675 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8927140 | AGCCTGGCCAACATA[C/G]TGAAACCCCGGCTCT | 7874 |
rs772787604 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8912969 | CGCAGCACAAAACCC[A/G]GAGAAAGGAGACTAG | 7874 |
rs772878454 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8913844 | CAGACTTAAACTCCA[A/G]GGCTCAAGCTATCCT | 7874 |
rs772897318 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8922576 | AGGGCCACTCTGTGG[C/T]GTGGCAGGGAGACTA | 7874 |
rs772898240 | snp | C/G | 1.91988e-05 | 0.00309823 | intron-variant, missense | USP7 | GRCh38.p7 | 16:8894509 | CACTTGTTTCTTAGT[C/G]TGAAACCCACACCAG | 7874 |
rs772902146 | snp | C/T | 1.64887e-05 | 0.00287125 | intron-variant | USP7 | GRCh38.p7 | 16:8905376 | GATCAAGCACTGTGA[C/T]AAGTACCCAACACTA | 7874 |
rs772911042 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8946152 | AAACCTCACACCTTA[C/T]ACAAAAGGTAGCTCA | 7874 |
rs772979828 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8909845 | GTAGAAGAATCACTT[C/G]AACCCAGGAGGCAGA | 7874 |
rs772983377 | snp | A/C | 1.67621e-05 | 0.00289495 | intron-variant | USP7 | GRCh38.p7 | 16:8917200 | ACTCTGAGAAGATGC[A/C]GGGGAATTTAAAAAA | 7874 |
rs772984697 | snp | A/G | 4.95291e-05 | 0.00497615 | intron-variant | USP7 | GRCh38.p7 | 16:8896970 | CACCCCTAACTGAAC[A/G]TCCACAATTGGGCTC | 7874 |
rs772992029 | in-del | -/GGC | 1.65014e-05 | 0.00287235 | intron-variant | USP7 | GRCh38.p7 | 16:8902062 | CTCTAAGTGCAGGCA[-/GGC]GTCTCGTGGGCACTT | 7874 |
rs772994786 | snp | A/C | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894082 | GTCGAGCCCTAGCCA[A/C]GGCCGAGGATGAGAC | 7874 |
rs773001089 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8945378 | AACACAGCAAGATGC[C/T]GTCTCAAACAAACAA | 7874 |
rs773044868 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8920010 | ACACTCGGAGAGGAC[A/T]TCCTCCCTGCCCTCA | 7874 |
rs773053812 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950535 | CCCAACTTGAGAACA[C/G]TGAAGACTTTGATCA | 7874 |
rs773076602 | snp | A/G | 1.6477e-05 | 0.00287024 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8915475 | GAATAATTTGGGTAT[A/G]GTGCCCTCTACACAG | 7874 |
rs773089159 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8904808 | TAAAATAAAAATAAA[A/G]TAAAATACAAAAAAT | 7874 |
rs773110130 | snp | A/T | 1.64732e-05 | 0.0028699 | intron-variant | USP7 | GRCh38.p7 | 16:8895021 | CACTCGGCCAACCAC[A/T]ACAGCATACCTGGTG | 7874 |
rs773131309 | snp | A/T | 1.6557e-05 | 0.00287719 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8899179 | GCCTCTGTGCAACTG[A/T]CTTTGCAACCTAAGA | 7874 |
rs773143396 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961185 | CTAAAAATTCAACAC[C/T]CTCTAGTCTTTTAAA | 7874 |
rs773145835 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8949750 | CCCATGCTGGCTTTC[C/T]TTACGCAGAGACACC | 7874 |
rs773149870 | snp | C/T | 1.79422e-05 | 0.00299513 | intron-variant | USP7 | GRCh38.p7 | 16:8902348 | ACGCCTTCTGCACGG[C/T]TCCAAACCAGATACG | 7874 |
rs773153852 | in-del | -/C | 1.66197e-05 | 0.00288263 | intron-variant | USP7 | GRCh38.p7 | 16:8904610 | CTGCAGATGGACTTT[-/C]CCCTCTTAGAAGCTC | 7874 |
rs773164542 | snp | G/T | 0.000164821 | 0.00907652 | intron-variant | USP7 | GRCh38.p7 | 16:8915356 | AGGACTGCAAATAAG[G/T]AAAGTAAAAGTGGTT | 7874 |
rs773181495 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8895276 | TAAAAAAACGCCACA[C/T]CTGGATCCAGCCAGA | 7874 |
rs773205019 | snp | C/T | 1.65652e-05 | 0.0028779 | intron-variant | USP7 | GRCh38.p7 | 16:8921120 | AACAACAAGCAGTAA[C/T]GCACCAATTGTTCAG | 7874 |
rs773205718 | snp | A/G | 1.6607e-05 | 0.00288153 | intron-variant | USP7 | GRCh38.p7 | 16:8894660 | AAGAAAAAAAATTAA[A/G]ACTCCTCCGTTATTT | 7874 |
rs773226588 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8948297 | AAGCAATCCTCCCAC[C/T]TCAGCCTCCAGAGTA | 7874 |
rs773238381 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8925645 | CGCAGAGGCCACCGC[A/G]CATCCGTCTCTGTGC | 7874 |
rs773254406 | snp | C/T | | | intron-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894401 | TAAGAACTCGTAGGT[C/T]ATGGAATGCTATTGC | 7874 |
rs773298982 | snp | A/C | 0.000102335 | 0.00715241 | intron-variant | USP7 | GRCh38.p7 | 16:8920456 | TCACTTCCTATAAAA[A/C]ATAAATAAGAATATC | 7874 |
rs773300608 | snp | A/C | 1.65304e-05 | 0.00287488 | intron-variant | USP7 | GRCh38.p7 | 16:8898458 | AAGAAAAGAAAGATT[A/C]ACATCAGATACCGTC | 7874 |
rs773305177 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892320 | TCCCTGCTTTCTATC[A/C]CACGGGTCACAAGGC | 7874 |
rs773315502 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8948809 | TCTAGAAAAAAAATA[C/T]AAAACTTAGCCAGGC | 7874 |
rs773334614 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8955991 | AGACACTTGCAGCCC[C/T]ACCCTGGGATGGGAC | 7874 |
rs773340888 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893581 | AAGTATAACTGAAGG[A/G]AATAGGTCAGACGAG | 7874 |
rs773341541 | snp | C/T | 0.000249221 | 0.0111601 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962437 | TCAAACTACAGTGCC[C/T]TGGAAAATTACTGCC | 7874 |
rs773390270 | snp | G/T | 1.64931e-05 | 0.00287163 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8917049 | CTTTGTTAACTTTTT[G/T]GTTCCTACAGGTTTA | 7874 |
rs773396524 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8955057 | CAGTGGTGTGTGGAC[C/G]AGTCACTATTAATCA | 7874 |
rs773402577 | snp | A/G | 3.36672e-05 | 0.00410274 | intron-variant | USP7 | GRCh38.p7 | 16:8900507 | TTAGTACAAAGTGAT[A/G]CAATCCTTCACAAAG | 7874 |
rs773410281 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8919324 | GAACTGGTGCAAATG[A/C]AACCCCCACATTCGC | 7874 |
rs773412355 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8917629 | GGGGATCTGCCCACC[A/T]TGGCCTCCCAAAGTG | 7874 |
rs773446120 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8897552 | CTAGAAAGGGTGAGA[C/G]ATCTAGCATCTAAAT | 7874 |
rs773460943 | snp | C/G | 5.00388e-05 | 0.00500169 | intron-variant | USP7 | GRCh38.p7 | 16:8920339 | CATTTTTAACAGCAC[C/G]TGATTAAAGAAAAAC | 7874 |
rs773465981 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8898247 | AGCCCCCATCATGTG[C/G]TGTTGTTTAGAGTGT | 7874 |
rs773503115 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8925018 | AGAAACTTGTTTAAG[A/G]TAATAACGTCTAGAA | 7874 |
rs773544233 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8902006 | GAAGAAGGCTTAACC[A/C]TGTGTGTTTAGAACA | 7874 |
rs773557136 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8932091 | TCTCCAAAACCCCAA[C/T]GCTTAGATTACATCA | 7874 |
rs773559199 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8922023 | GGACGCTGACACTGG[C/G]TATGGACCATTCACT | 7874 |
rs773561402 | snp | C/G | 3.34532e-05 | 0.00408968 | intron-variant | USP7 | GRCh38.p7 | 16:8901274 | GTTAAGATCCAAACA[C/G]TCAGCACAATGCTTA | 7874 |
rs773578036 | snp | A/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957615 | AAAAAAAATTAGCCA[A/T]ATGTGGTCACCCTGA | 7874 |
rs773584026 | snp | G/T | 6.59207e-05 | 0.00574073 | intron-variant | USP7 | GRCh38.p7 | 16:8901121 | AAATCTACTCAGAAG[G/T]TAAGTGCACGAAGGA | 7874 |
rs773588340 | in-del | -/TTT | 2.0508e-05 | 0.00320212 | utr-variant-5-prime, intron-variant, cds-indel | USP7 | GRCh38.p7 | 16:8936717 | TCTACCTCAGCATTC[-/TTT]TTTATTTTTTAAAGC | 7874 |
rs773593987 | in-del | -/ATC | | | intron-variant | USP7 | GRCh38.p7 | 16:8908813 | GAGAACCACAGAAAA[-/ATC]ATTAAATGGAAAATC | 7874 |
rs773653401 | snp | G/T | 1.65176e-05 | 0.00287376 | missense, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8930365 | TGATCACAGGGTTCT[G/T]AGTAATTCTTGGTGG | 7874 |
rs773674539 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8923310 | CACCATAATCTTCCA[C/T]GGCAGATTTCGCACA | 7874 |
rs773682528 | snp | G/T | 1.97027e-05 | 0.00313862 | intron-variant | USP7 | GRCh38.p7 | 16:8902502 | AAAAAATATTAAGAG[G/T]AGATTAAAATAAAAA | 7874 |
rs773730186 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8896893 | TGAGTCTGGGAATGA[C/T]GCGCATGGATCCCAG | 7874 |
rs773769650 | snp | C/T | 1.66601e-05 | 0.00288614 | intron-variant | USP7 | GRCh38.p7 | 16:8910856 | GAGAGAAAAGTCAAG[C/T]GCTAAAGCTTCATTT | 7874 |
rs773791739 | snp | C/T | 3.29527e-05 | 0.00405898 | intron-variant | USP7 | GRCh38.p7 | 16:8894747 | CAAGGCTTGAGCCTA[C/T]GGCCCGCCAAGCCCC | 7874 |
rs773798345 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950798 | TGTCTTCCCCAGGCA[C/G]TGACCAGCGCACGAC | 7874 |
rs773800153 | snp | A/C | 1.66092e-05 | 0.00288172 | intron-variant | USP7 | GRCh38.p7 | 16:8899213 | AGAAAGGAAGGTTCA[A/C]ATTTTGGGGAAAAAT | 7874 |
rs773804012 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8940069 | TGCCACTGAACTCCA[C/G]CATGGGTGACACAGC | 7874 |
rs773804616 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8908167 | GGTTGACCTCTGAAA[C/G]TTGACATAAAATCAT | 7874 |
rs773830453 | snp | A/G | 6.65037e-05 | 0.00576606 | intron-variant | USP7 | GRCh38.p7 | 16:8903253 | GTGGGGTATATCCAC[A/G]GGACCGGTACGCACC | 7874 |
rs773831692 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8927723 | TGCCTGTAATCCCAG[C/G]TACTCGGGAGGCTGA | 7874 |
rs773901125 | snp | C/G | 8.75791e-05 | 0.00661679 | intron-variant, missense | USP7 | GRCh38.p7 | 16:8894517 | TCTTAGTCTGAAACC[C/G]ACACCAGCCCCCGGG | 7874 |
rs773922289 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8926280 | GTCAGGAGTTTGAGA[A/C]CAGCCTGCCCAACAT | 7874 |
rs773930268 | snp | C/T | | | intron-variant, missense | USP7 | GRCh38.p7 | 16:8894433 | CCTGGTTCCACAGGT[C/T]GGCCAGTGGAGAGAG | 7874 |
rs773940975 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8905012 | ACATGAAATTACTTG[C/G]TACCATAAGTCTGCA | 7874 |
rs773990700 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8929075 | AAAAACAGTAGGGAA[A/T]TGTTGGAACAGATTG | 7874 |
rs773994792 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8938825 | CATAGCATTTACACT[A/G]TATTAGATATTATAA | 7874 |
rs774051943 | in-del | -/AT | | | intron-variant | USP7 | GRCh38.p7 | 16:8906900 | CAAATTCAGAAAGAC[-/AT]GTAAAAATATTTCCC | 7874 |
rs774067370 | in-del | -/CA | 1.64885e-05 | 0.00287123 | intron-variant | USP7 | GRCh38.p7 | 16:8915395 | AATAGTCAAAAAATT[-/CA]CATTCTAAAACCTTT | 7874 |
rs774085634 | in-del | -/C | 0.48 | 0.0979796 | intron-variant, frameshift-variant | USP7 | GRCh38.p7 | 16:8894525 | TGAAACCCACACCAG[-/C]CCCCGGGGGGGGGAG | 7874 |
rs774148484 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8907488 | CAAACTAATCAGGAT[-/A]AAAAATACTGTATTC | 7874 |
rs774160483 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8934352 | AGTGAATTCAGATTA[A/G]AGCTCAAAGAAGGGC | 7874 |
rs774160827 | snp | A/G/T | 3.30591e-05 | 0.00406554 | intron-variant | USP7 | GRCh38.p7 | 16:8899586 | GATCTGAAGAGGAAA[A/G/T]GAGCATTTATTAAAT | 7874 |
rs774169498 | snp | C/T | 8.25144e-05 | 0.00642265 | intron-variant | USP7 | GRCh38.p7 | 16:8895612 | GGCTCATGAATTCTC[C/T]CTGGTGCCAACAGTA | 7874 |
rs774190045 | in-del | -/TCA | 1.64731e-05 | 0.00286989 | cds-indel, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8905252 | CGAACAGACAGGTCG[-/TCA]TCGTGACCCCCATAA | 7874 |
rs774194105 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8943351 | CTACATGTATAGTCT[A/G]CTCCGCAAAAGAAAC | 7874 |
rs774200982 | snp | C/T | 1.67189e-05 | 0.00289122 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8906565 | TCATCAAGTGGTAAC[C/T]GCTCTGGGAATTCAA | 7874 |
rs774207376 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8911613 | GAGAGCCCCGTGATG[G/T]GCCCAGCTCTGCTGA | 7874 |
rs774275921 | snp | A/C/T | 3.29462e-05 | 0.00405857 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8895039 | AGCATACCTGGTGTA[A/C/T]CCTCAGCAAAAACGG | 7874 |
rs774304142 | snp | C/T | 0.000165076 | 0.00908355 | intron-variant | USP7 | GRCh38.p7 | 16:8908333 | CTTTATATCCCACTA[C/T]AGATTACCTATCATT | 7874 |
rs774387320 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8920968 | GACTAAAAAGTGAGA[C/T]GTGAATCCAGAAAGC | 7874 |
rs774409517 | snp | C/T | 1.76802e-05 | 0.00297318 | intron-variant | USP7 | GRCh38.p7 | 16:8923426 | TGTCTGCAAAAAAAA[C/T]ACATCATCAGTCACA | 7874 |
rs774410432 | snp | G/T | 0.00040197 | 0.0141712 | intron-variant | USP7 | GRCh38.p7 | 16:8910870 | GTGCTAAAGCTTCAT[G/T]TATAATGTAGCCAAC | 7874 |
rs774433299 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8951529 | GCTTGGAGAGAGCCC[A/C]TGGATATCCTATTTG | 7874 |
rs774447911 | snp | A/G | 3.29886e-05 | 0.00406118 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8915288 | ACTTAGCTGGATATC[A/G]TAATAATCTTCTCTT | 7874 |
rs774479245 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8920110 | AGTGTACATTCTTTA[C/G]GAACAGAAAACCACA | 7874 |
rs774515826 | snp | C/T | 1.67363e-05 | 0.00289272 | intron-variant | USP7 | GRCh38.p7 | 16:8906384 | AGAGCTTGTGTTAAC[C/T]TTCTGATGAGCTTGC | 7874 |
rs774542875 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8940812 | AGCCGGACATGGTGG[C/T]GCACACCTGTAATCC | 7874 |
rs774549629 | in-del | -/TGCTGCTGG | 6.56146e-05 | 0.00572739 | cds-indel, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8963268 | TTCTGCTGCTGCTGC[-/TGCTGCTGG]TGCTGCTGGTGGTTC | 7874 |
rs774564738 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8923806 | TGGGGGTAAAGACCA[C/T]GACATGGGACTTGGG | 7874 |
rs774583597 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8900242 | TCTAAGGAGTTTCGA[C/T]TTCATAAATCTCAGG | 7874 |
rs774602658 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8926587 | TACGAGGAATTACAT[C/G]AGACTCAGTGATGGA | 7874 |
rs774603600 | snp | C/T | 5.7474e-05 | 0.00536038 | intron-variant | USP7 | GRCh38.p7 | 16:8930434 | TCCACGGGTTTTACA[C/T]TCATGGCTTTAATAG | 7874 |
rs774609995 | snp | C/T | 6.58979e-05 | 0.00573974 | intron-variant | USP7 | GRCh38.p7 | 16:8894874 | GAATGGCAAAGGACA[C/T]GTGCTCACACAGTCA | 7874 |
rs774628428 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8940207 | CTGCTGCCTATCTAC[A/G]CATCCTATAGCCAGG | 7874 |
rs774632411 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8949545 | AAGCCTTGCCGCTGC[C/T]ATCCTTACCTCCAAA | 7874 |
rs774646200 | in-del | -/CA | 3.29511e-05 | 0.00405887 | intron-variant | USP7 | GRCh38.p7 | 16:8894880 | CAAAGGACATGTGCT[-/CA]CACAGTCACTCCCAG | 7874 |
rs774680665 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8917776 | TCCTACTTATTGGAG[C/T]ACCATTTCTTTTTTT | 7874 |
rs774688722 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892378 | TGCAGTGGAAGTTGA[A/G]AAAGGAAGTCACTCC | 7874 |
rs774699869 | snp | A/C | 3.76768e-05 | 0.00434016 | intron-variant | USP7 | GRCh38.p7 | 16:8898687 | TTGTTTATTTGCCTA[A/C]AAACAAATATCTGTG | 7874 |
rs774704270 | in-del | -/CGCCGAGGCAGGAGAATCG | | | intron-variant | USP7 | GRCh38.p7 | 16:8922385 | CCCAGCTACTTGAGA[-/CGCCGAGGCAGGAGAATCG]CTTGAACCCGGGAGG | 7874 |
rs774716205 | snp | C/T | 1.65206e-05 | 0.00287403 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8898573 | TCTAGGCTTGAAGAA[C/T]TGTAGAAGATCTCTT | 7874 |
rs774733250 | in-del | -/AGCTTTTTT | | | intron-variant | USP7 | GRCh38.p7 | 16:8955821 | AGGTCAATGGCTTAC[-/AGCTTTTTT]AAGGGGCTGTGGAGT | 7874 |
rs774767793 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8955621 | TGAGGCAGGGGAATC[A/G]CTTGAACCTGGGAGG | 7874 |
rs774794168 | snp | A/C/T | 3.29474e-05 | 0.00405867 | synonymous-codon, missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8919100 | AGTCGCTCCCTGATT[A/C/T]TTTAAGCCGACGTAG | 7874 |
rs774851878 | snp | C/T | 3.35632e-05 | 0.0040964 | intron-variant | USP7 | GRCh38.p7 | 16:8900511 | TACAAAGTGATACAA[C/T]CCTTCACAAAGTACA | 7874 |
rs774854341 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8922613 | GTGCAGTCCAAGTCA[A/G]CAGCTTCCCCTGGTT | 7874 |
rs774873948 | snp | A/G | 1.64852e-05 | 0.00287094 | intron-variant | USP7 | GRCh38.p7 | 16:8918985 | TGATATACCTGAGAA[A/G]AAAGGGTGAGCGGAA | 7874 |
rs774899607 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8948639 | AGTTCCACACGATGG[-/A]ATATTATTCTGCGAG | 7874 |
rs774911135 | snp | C/T | 3.2994e-05 | 0.00406152 | intron-variant | USP7 | GRCh38.p7 | 16:8916487 | AGAAATATACAAGTA[C/T]TGCTTGAAACTTACC | 7874 |
rs774938283 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8955132 | ATTTCTTCCCACGTA[C/T]GCTTGTTCTAAGAAT | 7874 |
rs774954910 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8909143 | GACTCTAAGCTCTTG[C/T]CCTGCTCTATCACTG | 7874 |
rs774955542 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8899311 | CCCTAGAAATTTATT[A/G]AACAGGAATAAACTA | 7874 |
rs774966807 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8909508 | GGATTCTGTCTCCAC[C/T]GCTGTCCACTGAGGC | 7874 |
rs774992818 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8896595 | ACTCAATCTGTCAAA[A/T]ACAAAATCAGGAGTC | 7874 |
rs775006924 | snp | A/T | 3.56271e-05 | 0.00422046 | intron-variant | USP7 | GRCh38.p7 | 16:8923429 | CTGCAAAAAAAACAC[A/T]TCATCAGTCACAGAG | 7874 |
rs775026435 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8929115 | AACTAGACCCGGAAT[C/G]TTCCGATAGGGCAGG | 7874 |
rs775035412 | snp | C/T | 1.65463e-05 | 0.00287626 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8930375 | GTTCTGAGTAATTCT[C/T]GGTGGGTCATCTGTA | 7874 |
rs775046325 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8943421 | AGTTGCAGCACGCAC[A/G]GCCGGAACCGAGCTG | 7874 |
rs775053055 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957884 | CTTTGTCTGGAAAAC[A/G]GGCTTTTACTTCCAA | 7874 |
rs775076251 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8895755 | GCCTGAACAGAGAGG[-/A]AAAAAAAATAGGGCA | 7874 |
rs775079273 | in-del | -/AAC | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956778 | AAAAAACAAAAACAA[-/AAC]AAAAAAAAAAACACT | 7874 |
rs775080697 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8895457 | GTCTGGATTGGGTTG[A/G]TAACCCAAACTGAGG | 7874 |
rs775111888 | snp | A/G | 1.64904e-05 | 0.00287139 | intron-variant | USP7 | GRCh38.p7 | 16:8895184 | GACACAGTTCTGTAA[A/G]TGCAAGTGATGTGGT | 7874 |
rs775149474 | snp | C/T | | | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891863 | GTTTTCAGGGCTCCC[C/T]GCTGTGAAGACTCCG | 7874 |
rs775157682 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8930276 | CCACTGCGAGGCGGT[A/G]AACCACAGGCACTTA | 7874 |
rs775166475 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8905734 | AGTTATCAAACTAAA[C/T]GAGCTGTTTTATCCT | 7874 |
rs775166718 | snp | A/G | 3.29468e-05 | 0.00405861 | missense, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8923332 | TTTCGCACAAAACAC[A/G]GAGGGCTAAGGACCG | 7874 |
rs775192097 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957805 | ACACAAAAACGATAA[C/T]AAAAATAGACTTTAC | 7874 |
rs775196339 | in-del | -/TT | | | intron-variant | USP7 | GRCh38.p7 | 16:8895841 | GTTACCACGATATGT[-/TT]TTTTTTTTTTTTTTG | 7874 |
rs775210942 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964653 | TTTAATTAGCCGGGT[A/G]TTGTGCCTCCTGCCT | 7874 |
rs775228223 | snp | C/T | 1.65715e-05 | 0.00287845 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8894635 | CATTACAATTGCAAA[C/T]TTAAACTAAAAGAAA | 7874 |
rs775237317 | snp | C/G/T | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8902174 | GGGTTTTCATTATCA[C/G/T]TGAGCTCAATCATCT | 7874 |
rs775240528 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8939433 | TTGACCATTCACTTG[A/C]TGACATCTGGGTCCT | 7874 |
rs775260666 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8925803 | TTAGATGACACTTCG[A/G]GTGTATTAAAATTTC | 7874 |
rs775260801 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8936093 | AACCCTGGTGTGTTG[A/C]AACTAAGAGTCCATG | 7874 |
rs775293780 | in-del | -/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8929080 | CAGTAGGGAAATGTT[-/G]GAACAGATTGCTCTG | 7874 |
rs775300723 | snp | C/T | 1.73387e-05 | 0.00294432 | intron-variant | USP7 | GRCh38.p7 | 16:8920472 | ATAAATAAGAATATC[C/T]AGCTTGAATAAGAAC | 7874 |
rs775306537 | snp | C/T | 1.71867e-05 | 0.00293139 | intron-variant | USP7 | GRCh38.p7 | 16:8901284 | AAACACTCAGCACAA[C/T]GCTTAAAAAACAAAA | 7874 |
rs775306808 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8958704 | ACTTCCCCACACTCA[C/T]CGCAGGGAGCTCTAG | 7874 |
rs775307564 | in-del | -/GGTTC | 1.65894e-05 | 0.00288 | intron-variant | USP7 | GRCh38.p7 | 16:8899207 | AGACACAGAAAGGAA[-/GGTTC]ACATTTTGGGGAAAA | 7874 |
rs775317216 | snp | A/C/G | 4.94844e-05 | 0.00497395 | intron-variant | USP7 | GRCh38.p7 | 16:8895629 | TGGTGCCAACAGTAT[A/C/G]GGGGACAGATACCTC | 7874 |
rs775343031 | snp | A/C/G | 3.29735e-05 | 0.00406028 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893951 | GTTCTAGGCTGTTAA[A/C/G]GGGCCACCCACACAC | 7874 |
rs775346968 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8935132 | TAATACCAAGTTTTA[C/T]ATGCCACCTTTTCGG | 7874 |
rs775357490 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8902849 | GCCAAGATCGCGCCA[C/G]TGGGCAACAAGAGTG | 7874 |
rs775368603 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8953446 | CTAAGTAAAGTCTGA[C/G]GTACGATCCAAGGGG | 7874 |
rs775380424 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8940575 | CATCAGAAAGGGAGA[A/G]GTGGGAGCCTGTAAG | 7874 |
rs775425753 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8922765 | GGACATTTCATAATA[C/T]ACATGAATGTTTAAA | 7874 |
rs775434475 | in-del | -/AAG | | | intron-variant | USP7 | GRCh38.p7 | 16:8919543 | TGTAGACACACACAC[-/AAG]AAGAAACAGAAGTGT | 7874 |
rs775435677 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8899893 | GGTTCCCCTTTGAGG[G/T]GGCCAGGCATCTGCC | 7874 |
rs775465927 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8905229 | ACATGTAAGCATTAG[C/T]GCAGTGTCGAACAGA | 7874 |
rs775496192 | snp | C/T | 1.69375e-05 | 0.00291006 | intron-variant | USP7 | GRCh38.p7 | 16:8900657 | GATATAAAATTGTTA[C/T]ACTGCAAGTTTGTCT | 7874 |
rs775500105 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8955979 | AGATTACCACCCAGA[C/G]ACTTGCAGCCCCACC | 7874 |
rs775549727 | snp | A/C/G | 0.00195122 | 0.0311737 | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962532 | GGCAGGGCTTTCGCA[A/C/G]GGTTGCAAGCGCACA | 7874 |
rs775578779 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950468 | TAAGAGTAAATGCAG[A/G]TGTGTGGTGCTAATT | 7874 |
rs775582509 | in-del | -/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8920994 | AAGCTGCTAAAAACG[-/T]TAAGATACGAAACTG | 7874 |
rs775584853 | snp | A/G | 3.30278e-05 | 0.0040636 | intron-variant | USP7 | GRCh38.p7 | 16:8930449 | TTCATGGCTTTAATA[A/G]AATAAGCAAAATATA | 7874 |
rs775600919 | snp | A/C/T | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8904511 | TTCTCTTCTTGTAAT[A/C/T]GCTCCACCAACTGCT | 7874 |
rs775622202 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8911787 | AGTTTCTTCCGAAGC[C/T]GTCAGTGAGAACTGA | 7874 |
rs775623154 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8942818 | CTCCAAAAGTGTTGG[C/G]GTTACAGACATGAGC | 7874 |
rs775678361 | in-del | -/AAAG | | | intron-variant | USP7 | GRCh38.p7 | 16:8926513 | TAGGAGGGCCAAAAA[-/AAAG]GAGAAGTGGACTTGG | 7874 |
rs775681581 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8933162 | TCAGACTGGTCTCAA[A/G]CTCCTGACCTCAAGT | 7874 |
rs775707938 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8916106 | ATGCTGAGGTCTGCT[A/C]AATGAGAACCTCGCT | 7874 |
rs775739260 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8919493 | ATCACACGCAAGGTC[A/G]GCACAACGTGGAAAA | 7874 |
rs775754567 | snp | A/G | 5.09411e-05 | 0.00504658 | intron-variant, synonymous-codon | USP7 | GRCh38.p7 | 16:8894539 | GCCCCCGGGGGGGGG[A/G]GAACCCTTACCGGGC | 7874 |
rs775796152 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8932221 | TTTAAGACATTAAAG[A/T]TCAATTTCAGTCTTG | 7874 |
rs775823476 | in-del | -/TG | | | downstream-variant-500B, intron-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8891817 | CGTGGGAAGGGCCAC[-/TG]TGACCGCAGGCCCTT | 7874 |
rs775840362 | snp | C/G | 0.000201076 | 0.0100248 | intron-variant | USP7 | GRCh38.p7 | 16:8920317 | TCTTTCACTGCAGCA[C/G]AAAAGACATTTTTAA | 7874 |
rs775863478 | snp | C/T | 6.59044e-05 | 0.00574002 | intron-variant | USP7 | GRCh38.p7 | 16:8894880 | CAAAGGACATGTGCT[C/T]ACACAGTCACTCCCA | 7874 |
rs775886164 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8940894 | ACCTGGAATATATAC[A/C]GTCTCCAGAACCTGG | 7874 |
rs775890721 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8946994 | AGGTAATGGGGCGGG[C/G]TGAATTAACCTTCAT | 7874 |
rs775928437 | snp | A/T | 6.20405e-05 | 0.00556924 | missense, utr-variant-5-prime, intron-variant | USP7 | GRCh38.p7 | 16:8936612 | CTGTGGTTCCCAGCC[A/T]TCTCTGCATGGCTCT | 7874 |
rs775936720 | snp | C/T | 1.66352e-05 | 0.00288398 | intron-variant | USP7 | GRCh38.p7 | 16:8917174 | GAAACAATTAAGAAA[C/T]AAGAATTTTTACTCT | 7874 |
rs775955485 | snp | A/T | 1.65288e-05 | 0.00287474 | intron-variant | USP7 | GRCh38.p7 | 16:8908325 | AATCTTAACTTTATA[A/T]CCCACTATAGATTAC | 7874 |
rs775957710 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961617 | TAATTCTCACTAGTG[C/T]CCAAAAACACCTGGA | 7874 |
rs775974753 | snp | C/G | 9.90671e-05 | 0.00703731 | intron-variant | USP7 | GRCh38.p7 | 16:8897114 | CCTAAGTAATGAAAA[C/G]ATAAAATAAGTGCTT | 7874 |
rs775979833 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8945306 | CAAGAATCGTTTGTA[C/G]CTGGGAGGTGGAGGT | 7874 |
rs775992795 | snp | C/T | 1.67203e-05 | 0.00289134 | intron-variant | USP7 | GRCh38.p7 | 16:8900984 | GGAAAAATAAACCAT[C/T]CAAACCTCATAGAGG | 7874 |
rs776001434 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8915119 | GCCTGTGTTCACCCA[A/G]TGAGCTGTTTGCTTA | 7874 |
rs776067441 | in-del | -/A | 1.69596e-05 | 0.00291196 | intron-variant | USP7 | GRCh38.p7 | 16:8900970 | ATATACTAATTATGG[-/A]AAAAATAAACCATCC | 7874 |
rs776078669 | snp | A/G | | | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8905251 | TCGAACAGACAGGTC[A/G]TCATCGTGACCCCCA | 7874 |
rs776087668 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8923888 | CAGCCATTCCCCTGG[A/C]AGCTCAGCACTGCTC | 7874 |
rs776115153 | snp | A/C/G/T | 0.000142142 | 0.00842942 | intron-variant | USP7 | GRCh38.p7 | 16:8906604 | GAAAACATTTTAAAA[A/C/G/T]AAATTCAGTATTAAT | 7874 |
rs776148648 | in-del | -/TGACAAC | 1.68173e-05 | 0.00289972 | intron-variant | USP7 | GRCh38.p7 | 16:8903435 | AGCACAGAAAAGACT[-/TGACAAC]TGACAAAAAATGAGT | 7874 |
rs776150203 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8960069 | CGACCATCTGAGTAT[G/T]CAGAGGGCAGAGACC | 7874 |
rs776205097 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8896817 | ACTTGAAAAACTGGA[C/G]CAACACTGGGTCTGT | 7874 |
rs776232482 | in-del | -/TTT | | | intron-variant | USP7 | GRCh38.p7 | 16:8895840 | AGTTACCACGATATG[-/TTT]TTTTTTTTTTTTTTG | 7874 |
rs776242814 | snp | C/T | 4.94588e-05 | 0.00497262 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893955 | TAGGCTGTTAAGGGG[C/T]CACCCACACACCGTC | 7874 |
rs776271430 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8944360 | GAACAAAGGAATTGC[C/G]TGGGCTATTTGTGGC | 7874 |
rs776288683 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8921599 | GCTTCTACTGCCGAT[A/G]TAGGGGTCACCTCTC | 7874 |
rs776292161 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8931393 | TGGTTTCACCATGTC[A/G]GTCAACTGGTCTCGA | 7874 |
rs776295236 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8911704 | GAGGAGCTCAAGGGA[A/G]CGGGAACCTGCTGGG | 7874 |
rs776311843 | in-del | -/ACTG | | | intron-variant | USP7 | GRCh38.p7 | 16:8945572 | CATAAGAGGAAAATC[-/ACTG]AGACTGGGGACATAC | 7874 |
rs776318940 | snp | A/G | | | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962771 | GCGCGCCCTCCGGGG[A/G]AGCGCACCGGAGCAG | 7874 |
rs776332059 | snp | A/C/G | 7.30119e-05 | 0.00604163 | intron-variant | USP7 | GRCh38.p7 | 16:8895753 | CAGCCTGAACAGAGA[A/C/G]GAAAAAAAAATAGGG | 7874 |
rs776413469 | snp | C/T | 3.33456e-05 | 0.0040831 | intron-variant | USP7 | GRCh38.p7 | 16:8930265 | CAAGTTTCCGCCCAC[C/T]GCGAGGCGGTGAACC | 7874 |
rs776415718 | in-del | -/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8923705 | TACTAAAGCTGAATT[-/C]CCCAAGGACCCCAGG | 7874 |
rs776421304 | snp | C/G | 1.64914e-05 | 0.00287149 | intron-variant | USP7 | GRCh38.p7 | 16:8895632 | TGCCAACAGTATCGG[C/G]GACAGATACCTCTAT | 7874 |
rs776423056 | snp | C/T | 1.69545e-05 | 0.00291152 | intron-variant | USP7 | GRCh38.p7 | 16:8900496 | AAATCCTGAAATTAG[C/T]ACAAAGTGATACAAT | 7874 |
rs776441351 | snp | C/T | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8899740 | GGTAATTCACTGTTA[C/T]CATTTTCAGGGTCAT | 7874 |
rs776444978 | snp | A/T | 1.65323e-05 | 0.00287505 | intron-variant | USP7 | GRCh38.p7 | 16:8902034 | ACAACAATCCAGGAA[A/T]CCAACGCTACTGCTC | 7874 |
rs776453439 | snp | C/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894069 | CTTTGTTGAAGTGGT[C/G]GAGCCCTAGCCAAGG | 7874 |
rs776465700 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8936225 | AGTGATCAAAACTAC[A/G]GCTGTTATTACGGCA | 7874 |
rs776475635 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8913784 | GAGAGAGATACTTGC[G/T]CTGTTGCCCAGGCTG | 7874 |
rs776485342 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8928046 | TAGTGAATAAGGAAC[C/T]AAAAGTAGAATGAGT | 7874 |
rs776494481 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8926834 | AACTTCTACAAACTG[G/T]TGTCACCACAAATCC | 7874 |
rs776499886 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8923681 | TTCCACATGAGAACA[A/C]TGTCTACTTTACTAA | 7874 |
rs776507510 | in-del | -/GGGCAC | | | intron-variant | USP7 | GRCh38.p7 | 16:8908983 | AACCCATATATCACA[-/GGGCAC]GCCCTTAGGGCTTAT | 7874 |
rs776528267 | snp | A/C | 1.65471e-05 | 0.00287633 | intron-variant | USP7 | GRCh38.p7 | 16:8897135 | ATAAGTGCTTTCAAG[A/C]AAGCATAAAAGGTCT | 7874 |
rs776559358 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8959809 | TTGGAAGAAACCCAC[C/G]ACCACCCCCGTAACA | 7874 |
rs776571187 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937039 | CCAAAATTAAAAGCT[A/G]ATTTTAAAAAGGCAA | 7874 |
rs776580230 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8900445 | AACGTGGCTCGGGAT[A/C]TAGGTACAAATGTTT | 7874 |
rs776587692 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8917561 | TTTATGAATTTTCAG[A/G]AGAGACAGGGTTTTG | 7874 |
rs776590932 | snp | A/T | 1.65479e-05 | 0.0028764 | intron-variant | USP7 | GRCh38.p7 | 16:8921132 | TAATGCACCAATTGT[A/T]CAGACTAAATACACT | 7874 |
rs776594063 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8959781 | CTTCAGCAGAAAAGT[-/A]AACTGCACAAGTTTG | 7874 |
rs776602318 | snp | C/T | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8902151 | CTGTTTCCAGGAATA[C/T]TGTCCAAGGGTTTTC | 7874 |
rs776606631 | in-del | -/T | 2.93794e-05 | 0.0038326 | intron-variant | USP7 | GRCh38.p7 | 16:8895793 | GTATATATATTCACA[-/T]AAAAATAAAATGGTT | 7874 |
rs776607841 | snp | A/G | 1.64838e-05 | 0.00287083 | intron-variant | USP7 | GRCh38.p7 | 16:8905361 | ACACACACCAGCAGC[A/G]ATCAAGCACTGTGAC | 7874 |
rs776634188 | snp | A/C | 1.67133e-05 | 0.00289074 | intron-variant | USP7 | GRCh38.p7 | 16:8920332 | CAAAAGACATTTTTA[A/C]CAGCACCTGATTAAA | 7874 |
rs776661524 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8934331 | GTGAAATCAGACTGA[C/G]ACACAAGTGAATTCA | 7874 |
rs776670403 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892508 | GCCCCGAAGGGCCTC[A/G]TGACACATCAGGTCA | 7874 |
rs776690065 | snp | C/T | 1.65192e-05 | 0.00287391 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8901026 | ATCTTGAATAAATCC[C/T]GCTCTGTCACACATA | 7874 |
rs776698120 | in-del | -/A | 1.64836e-05 | 0.0028708 | intron-variant | USP7 | GRCh38.p7 | 16:8916568 | CCACCTTTCAAAGAT[-/A]AAACAAACAACTCCA | 7874 |
rs776721993 | snp | C/G | 6.59131e-05 | 0.0057404 | utr-variant-5-prime, intron-variant | USP7 | GRCh38.p7 | 16:8936626 | CATCTCTGCATGGCT[C/G]TGCAGTGGCCTCTGC | 7874 |
rs776725416 | snp | C/T | 1.6483e-05 | 0.00287076 | intron-variant | USP7 | GRCh38.p7 | 16:8901114 | CTGAGCAAAATCTAC[C/T]CAGAAGGTAAGTGCA | 7874 |
rs776749401 | snp | A/G | 1.64846e-05 | 0.0028709 | intron-variant | USP7 | GRCh38.p7 | 16:8895161 | ATTTCCTGGGGACAC[A/G]GACAACAGACACAGT | 7874 |
rs776757710 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8902918 | TCTAAGAAAAAGAAT[G/T]CTAATTCTTCCCCGG | 7874 |
rs776795510 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8901075 | AGGAGAAAGAAGATA[C/T]TTTAAATGTGTAGCT | 7874 |
rs776804543 | snp | C/T | 1.79011e-05 | 0.00299169 | intron-variant | USP7 | GRCh38.p7 | 16:8923431 | GCAAAAAAAACACAT[C/T]ATCAGTCACAGAGCC | 7874 |
rs776822507 | snp | A/G | 1.66966e-05 | 0.00288929 | intron-variant | USP7 | GRCh38.p7 | 16:8903238 | ACGTTGGGAGCCACG[A/G]TGGGGTATATCCACG | 7874 |
rs776850157 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8924919 | GCTGAAAGAGGCGCA[A/T]CTTGTCCAAAATAAT | 7874 |
rs776872436 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8907066 | CAAGTTAGACGGGTG[A/G]GGGCTGGTCTCAAGC | 7874 |
rs776880202 | snp | C/G | 1.82052e-05 | 0.00301699 | intron-variant | USP7 | GRCh38.p7 | 16:8936550 | CTCCATCCATCACCA[C/G]CATAAGGAGCTCAAC | 7874 |
rs776884371 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8948865 | GCTACTCGGGAGGCT[A/G]ATGGGAGAGGATGGC | 7874 |
rs776924776 | in-del | -/CCC | | | intron-variant | USP7 | GRCh38.p7 | 16:8925660 | GCATCCGTCTCTGTG[-/CCC]CCGAGTGTGGCACTG | 7874 |
rs776940122 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8924232 | ACAAACCCTGCAGCA[A/T]CTTACTGCTTCCCAA | 7874 |
rs776949671 | snp | A/G | 0.000156864 | 0.0088548 | intron-variant | USP7 | GRCh38.p7 | 16:8930409 | CCCGCTTTAAAGAAG[A/G]AAAAGAAATTCCACG | 7874 |
rs776966638 | snp | C/G | 3.31983e-05 | 0.00407407 | intron-variant | USP7 | GRCh38.p7 | 16:8904598 | CCTCTTTGACCCCTG[C/G]AGATGGACTTTCCCC | 7874 |
rs776987761 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8946963 | AAAAATCCACTGAAA[C/G]TGCATGACGAACTTA | 7874 |
rs777039573 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8939585 | GCAACAATGCAGACA[C/T]AGATAAGGAGAAATC | 7874 |
rs777052576 | snp | C/G | 1.64749e-05 | 0.00287005 | missense, splice-acceptor-variant | USP7 | GRCh38.p7 | 16:8904525 | TCGCTCCACCAACTG[C/G]TGAGGAATATCATGG | 7874 |
rs777057526 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8895585 | TGTGATATTTAAATA[C/T]GCAGCAGATGGGGCT | 7874 |
rs777093513 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964792 | GAGACCCTGTCTCAA[C/G]TAATAGTGATAATAA | 7874 |
rs777129138 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8938933 | AAGACTTGAGCATCT[A/G]TGGATTTTGACACCC | 7874 |
rs777157241 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8906003 | GCCAAATGAGTATGG[C/T]GCCCTCTACACTCCC | 7874 |
rs777160592 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8914932 | CAACAGCGAAATAAA[C/T]AAACAAATACATCCT | 7874 |
rs777179326 | snp | A/C | | | intron-variant, nc-transcript-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8962622 | GGATTCGGAAACCAA[A/C]AGCGCCCGGGTCAGA | 7874 |
rs777180151 | in-del | -/AC | | | intron-variant | USP7 | GRCh38.p7 | 16:8915958 | GCTGCAAAAAAGAAA[-/AC]ACACCTTGCCCAGCC | 7874 |
rs777202195 | snp | A/T | 3.30589e-05 | 0.00406551 | intron-variant | USP7 | GRCh38.p7 | 16:8898452 | GCTATTAAGAAAAGA[A/T]AGATTCACATCAGAT | 7874 |
rs777209136 | in-del | -/T | 1.66471e-05 | 0.00288501 | intron-variant | USP7 | GRCh38.p7 | 16:8917179 | ATTAAGAAATAAGAA[-/T]TTTTTACTCTGAGAA | 7874 |
rs777209621 | in-del | -/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8930636 | CACTATAATTTGCTT[-/T]ATTTGCAATGATATT | 7874 |
rs777247017 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8916631 | AAGTAACTTAGATTG[A/C]AAACCTAAACTGGAT | 7874 |
rs777261899 | snp | C/T | 0.000165134 | 0.00908513 | intron-variant | USP7 | GRCh38.p7 | 16:8908330 | TAACTTTATATCCCA[C/T]TATAGATTACCTATC | 7874 |
rs777266614 | snp | C/T | 0.000148249 | 0.00860829 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8919058 | ATTCGTGAAAAATAA[C/T]GTCTGTAGCAGGCTG | 7874 |
rs777278476 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8924648 | AACAACCCTTCAGAC[A/T]CCAAAGTTCACTAAC | 7874 |
rs777282725 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8952748 | GGAGCATCATTCTGC[-/A]AACCACAGACCCTAA | 7874 |
rs777293299 | snp | A/G | 3.29913e-05 | 0.00406135 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8904450 | CTGCACTTGCATATA[A/G]AGATGGGCTTCCTGC | 7874 |
rs777308903 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957227 | AAAAATGGCATAACT[G/T]ACTTTCTTGCCTACG | 7874 |
rs777328662 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8916167 | AACAGAAGTCACCAC[C/T]GTACAGTGACTCAGG | 7874 |
rs777333589 | in-del | -/A | 1.67518e-05 | 0.00289407 | intron-variant | USP7 | GRCh38.p7 | 16:8910871 | GCTAAAGCTTCATTT[-/A]ATAATGTAGCCAACA | 7874 |
rs777360458 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8923653 | ATACACTTGCCATCC[C/T]TGTCAGACTGAGTTC | 7874 |
rs777361076 | snp | A/T | 1.69324e-05 | 0.00290962 | missense, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8923408 | CCTCGGAGCGCCAAC[A/T]GGTGTCTGCAAAAAA | 7874 |
rs777390528 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8946861 | CAACTTTTTAATATA[A/T]CTGTATAATAAAATG | 7874 |
rs777412615 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8929792 | AGTATGCTTTCTCAC[A/C]GAGAAGCTATAGACC | 7874 |
rs777463630 | snp | C/T | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8897074 | TCCCGGACACACCCA[C/T]GCTTGTCTGGATATA | 7874 |
rs777517375 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8952091 | ACCCCCCCGTCTATA[C/T]AAAAAAGAAAAAAAA | 7874 |
rs777543299 | snp | C/T | 9.72337e-05 | 0.0069719 | missense, utr-variant-5-prime, intron-variant | USP7 | GRCh38.p7 | 16:8936586 | AACCTGACTCACCTT[C/T]CAGCCCAAGCCTGTG | 7874 |
rs777564543 | snp | A/C | 1.68145e-05 | 0.00289948 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8908442 | GAATTTCACACCTTT[A/C]TCTGCTTCCTAAACA | 7874 |
rs777622858 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8910316 | CACAACCCTAGAGAA[C/G]ACACTACTCATTCTA | 7874 |
rs777639333 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8899069 | AGATGTTTCAATGAA[A/C]TGTGGAAAGCATGCA | 7874 |
rs777663313 | in-del | -/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8900821 | TGATTCTACAACAGG[-/T]TAAAAAAAAAAAATT | 7874 |
rs777664714 | in-del | -/GGTTCATGTCCCTTA | | | intron-variant | USP7 | GRCh38.p7 | 16:8941960 | GACAGCCACAGGGCT[-/GGTTCATGTCCCTTA]GTCATGAAGGAGGAG | 7874 |
rs777685027 | snp | A/C | 3.29462e-05 | 0.00405857 | splice-acceptor-variant | USP7 | GRCh38.p7 | 16:8902483 | ATCTTGTGGAAATCC[A/C]TGAAAAAAATATTAA | 7874 |
rs777700743 | in-del | -/C | 0.48 | 0.0979796 | intron-variant, frameshift-variant | USP7 | GRCh38.p7 | 16:8894524 | TGAAACCCACACCAG[-/C]CCCCCGGGGGGGGGA | 7874 |
rs777757065 | in-del | -/TTGT | 5.42476e-05 | 0.00520777 | intron-variant | USP7 | GRCh38.p7 | 16:8898672 | ATATAAATAAATGAC[-/TTGT]TTATTTGCCTAAAAA | 7874 |
rs777782547 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8939217 | CCTGAACAGTTCCAA[C/T]ACCACAAGGATCCCT | 7874 |
rs777783816 | snp | A/T | 1.6531e-05 | 0.00287493 | intron-variant | USP7 | GRCh38.p7 | 16:8906632 | AATTTACACAAAAAA[A/T]ATCACACTTTACAGT | 7874 |
rs777787871 | snp | C/T | 1.67556e-05 | 0.0028944 | intron-variant | USP7 | GRCh38.p7 | 16:8898341 | AAAAATTAAAATTCA[C/T]AGTATTAAAAAAACT | 7874 |
rs777815701 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8936894 | CCAGTTCCTTGGCTG[C/T]GACAAATCTGGTTTA | 7874 |
rs777829028 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8915874 | AAGAGATTAATGAGG[C/T]TGAGCCTGTCAACAG | 7874 |
rs777830586 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8902829 | AAAGGCGGAGGTTGC[A/G]GTGAGCCAAGATCGC | 7874 |
rs777867267 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8905218 | GATGTAGACTAACAT[A/G]TAAGCATTAGTGCAG | 7874 |
rs777872147 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938413 | ATTCAACAAACCGCA[C/T]ATCAAAAACACTCAG | 7874 |
rs777890601 | snp | A/C/G/T | 0.000301218 | 0.0122693 | intron-variant, synonymous-codon | USP7 | GRCh38.p7 | 16:8894533 | ACACCAGCCCCCGGG[A/C/G/T]GGGGGAGAACCCTTA | 7874 |
rs777893454 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8962062 | GTGAACACCAGTCAC[A/G]CTTAAGTGTTCCCAC | 7874 |
rs777895260 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8926563 | ATACGGCCAGCCAGA[C/T]TGTCCTCCTACGAGG | 7874 |
rs777900043 | snp | G/T | 3.29495e-05 | 0.00405877 | intron-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894115 | ATTACCTGGTGGGGA[G/T]GAAGAAAAGCAAGTG | 7874 |
rs777901881 | snp | A/C | 3.30535e-05 | 0.00406518 | intron-variant | USP7 | GRCh38.p7 | 16:8896950 | CAGAGGTCAGCGTTA[A/C]CTGCCACCCCTAACT | 7874 |
rs777978830 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8959461 | GCCTGAAAGAATCAG[A/G]AGAGCTGGAGCCTGG | 7874 |
rs777990074 | snp | C/G | 1.65474e-05 | 0.00287636 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8895709 | TCTTCTTGATGAACA[C/G]CAATGATTTTGTAGC | 7874 |
rs778044933 | snp | A/G | 1.64784e-05 | 0.00287035 | intron-variant | USP7 | GRCh38.p7 | 16:8902073 | GGCAGGCGTCTCGTG[A/G]GCACTTACGATCTTT | 7874 |
rs778048830 | snp | A/G | 6.59076e-05 | 0.00574016 | intron-variant | USP7 | GRCh38.p7 | 16:8905340 | TACACCACTGCAAGG[A/G]AAACAACACACACCA | 7874 |
rs778073082 | snp | A/G | 1.6486e-05 | 0.00287102 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8917136 | CGAATCATCCCCCTC[A/G]GTTGGCATCATGTAC | 7874 |
rs778082711 | snp | C/T | 1.64746e-05 | 0.00287002 | intron-variant | USP7 | GRCh38.p7 | 16:8894865 | CTCGCCCTAGAATGG[C/T]AAAGGACATGTGCTC | 7874 |
rs778090894 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8919238 | CAGCCTTAAGGAAAC[C/T]GAGGCCAGGAACACT | 7874 |
rs778144336 | in-del | -/TTT | | | utr-variant-3-prime, nc-transcript-variant, cds-indel | USP7 | GRCh38.p7 | 16:8893120 | ACAATTCATTTTTCC[-/TTT]TTTTTTCATTTTTAA | 7874 |
rs778148581 | snp | G/T | 1.70656e-05 | 0.00292104 | intron-variant | USP7 | GRCh38.p7 | 16:8903453 | CAACTGACAAAAAAT[G/T]AGTCCACACTGAACA | 7874 |
rs778177018 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8949502 | GACATACCCAGGACA[C/G]CCTGTGCTTCTATTT | 7874 |
rs778183055 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8927835 | AACAAGAACCTATCT[A/C]AAAATAAAATAAAAT | 7874 |
rs778183883 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8922255 | GCACTTTGGCAGGCC[A/G]AGACAGGCAGATCAC | 7874 |
rs778197980 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8941501 | GCCCACCCTCTTCTC[A/G]CAGGTCAACCGACAT | 7874 |
rs778217447 | snp | A/C | 1.66757e-05 | 0.00288749 | intron-variant | USP7 | GRCh38.p7 | 16:8915240 | TCATGCCATTAGATA[A/C]ACACAACACTTACTA | 7874 |
rs778269375 | in-del | -/TA | 0.00201641 | 0.0316882 | intron-variant | USP7 | GRCh38.p7 | 16:8903244 | GGAGCCACGGTGGGG[-/TA]TATCCACGGGACCGG | 7874 |
rs778281068 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8939387 | CCTTTCTCCTGTACT[C/G]TAGGATATCATGGCA | 7874 |
rs778282393 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8909387 | CTTTGGTGTACATCA[C/G]CTCATTTAAGAGGAC | 7874 |
rs778289673 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950098 | ATCTTATTCAATTTA[A/G]TTTTATTTAAATAGC | 7874 |
rs778315637 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893152 | ACTTTTTTACAAAGT[C/T]GACAGCTTACTAACC | 7874 |
rs778316489 | snp | A/C/T | 3.30514e-05 | 0.00406507 | intron-variant | USP7 | GRCh38.p7 | 16:8923179 | ATTGCACTAGGCTGA[A/C/T]CAAATTTGGCTTCCA | 7874 |
rs778348736 | snp | C/T | 1.65526e-05 | 0.00287681 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8894622 | GGTGTCGGCCCATCA[C/T]TACAATTGCAAATTT | 7874 |
rs778367249 | snp | C/G/T | 3.31781e-05 | 0.00407286 | missense, synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8898372 | TACCTCTTCCCTAAA[C/G/T]TGGCTGTTTAACCAT | 7874 |
rs778373705 | in-del | -/A | 0.000133439 | 0.00816711 | intron-variant, frameshift-variant | USP7 | GRCh38.p7 | 16:8894539 | GCCCCCGGGGGGGGG[-/A]GAACCCTTACCGGGC | 7874 |
rs778374898 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8918836 | GGTTGGCGGTGGTAA[C/G]TCTGAATCACTGAGG | 7874 |
rs778380029 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8918461 | GCTGTTAATGGATTA[G/T]ATGTTTTTCTAAATA | 7874 |
rs778405653 | in-del | -/TATG | | | intron-variant | USP7 | GRCh38.p7 | 16:8948911 | AAGGCTGCAATGAGC[-/TATG]TATGATCAAACCACG | 7874 |
rs778434797 | in-del | -/CGAT | | | intron-variant | USP7 | GRCh38.p7 | 16:8917293 | TGTTAGGGCTTTTAA[-/CGAT]CGATCCCCAAATTGG | 7874 |
rs778438208 | in-del | -/G | 5.65296e-05 | 0.00531617 | intron-variant | USP7 | GRCh38.p7 | 16:8923454 | CAGAGCCTGTGCATT[-/G]GACCAAAAGCACTAG | 7874 |
rs778455675 | snp | A/C/G | 3.30209e-05 | 0.00406319 | intron-variant | USP7 | GRCh38.p7 | 16:8902218 | ACGCTGATTTTAGAA[A/C/G]AGTCTAATGGCTTAG | 7874 |
rs778455957 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960682 | CTGACCAGGACCCCA[C/T]TCACAGCCTGGTCCA | 7874 |
rs778481945 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8948538 | ACTGCAAAAAAAGTT[A/C]AAATCCCTTTAAAAA | 7874 |
rs778491661 | snp | C/G | 8.87351e-05 | 0.00666031 | utr-variant-5-prime, intron-variant | USP7 | GRCh38.p7 | 16:8936681 | CCCACATCAGAGTGA[C/G]TGCATAGAATCTCTA | 7874 |
rs778515060 | snp | A/C | 1.72829e-05 | 0.00293959 | intron-variant | USP7 | GRCh38.p7 | 16:8908474 | TGAAAAACAAATGCA[A/C]ATGTAGTTAGCCTCT | 7874 |
rs778526450 | in-del | -/ATAGT | | | intron-variant | USP7 | GRCh38.p7 | 16:8944515 | AGGAGATTTTTATAC[-/ATAGT]ATACTCTTGGTTGTG | 7874 |
rs778536548 | snp | A/C/G | 0.000109602 | 0.00740204 | intron-variant | USP7 | GRCh38.p7 | 16:8916989 | AAAAAAAAAAAAAGA[A/C/G]GAAGCAGAATGGCAA | 7874 |
rs778545011 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8954755 | TCTGAGGTGGGTGGA[C/T]CAGGAGATCGAGACC | 7874 |
rs778562986 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950154 | ATATGGCCATGGAGA[C/T]CAAAAAACCAAATAT | 7874 |
rs778564825 | snp | C/T | 3.29837e-05 | 0.00406088 | intron-variant | USP7 | GRCh38.p7 | 16:8901090 | TTTTAAATGTGTAGC[C/T]GTAATGTACTGAGCA | 7874 |
rs778568744 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957363 | ACATGGCAAGAAATA[C/T]GTTGTTACAACTCTT | 7874 |
rs778581601 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8931402 | CATGTCGGTCAACTG[A/G]TCTCGAACTCCTGGC | 7874 |
rs778610049 | snp | A/G | 1.6486e-05 | 0.00287102 | intron-variant | USP7 | GRCh38.p7 | 16:8899806 | AAGTCCATGGCAGGG[A/G]GTAGCTGGTAAAAAT | 7874 |
rs778620228 | in-del | -/A/C/T | 0.000803769 | 0.0200329 | intron-variant, frameshift-variant | USP7 | GRCh38.p7 | 16:8894534 | ACCAGCCCCCGGGGG[-/A/C/T]GGGGAGAACCCTTAC | 7874 |
rs778665891 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8924799 | AAAAGCATGTGTGAC[A/G]GTAAGCACTTCTACC | 7874 |
rs778680603 | snp | A/C | 1.6534e-05 | 0.00287519 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8920398 | TGTACAAAGACTTCA[A/C]AGGTAACTTTGTCAT | 7874 |
rs778689457 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8908502 | TCTACTTACTCCTGG[A/G]AGCAATGAAAGCAAC | 7874 |
rs778702214 | snp | A/G | 4.94629e-05 | 0.00497283 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8903290 | TGAGAGAGGCTCTGA[A/G]CAAACTCAGCAAGCG | 7874 |
rs778772761 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8901650 | GGGTCAGCAAATTCC[A/G]ATCCACCTGTTTTGT | 7874 |
rs778779222 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8910995 | TAAATGTGCTGTTAG[C/T]ACCTTTGCTCATTGG | 7874 |
rs778803654 | snp | A/G | 5.01995e-05 | 0.00500972 | intron-variant | USP7 | GRCh38.p7 | 16:8930252 | ACCTGTTTTCTGACA[A/G]GTTTCCGCCCACTGC | 7874 |
rs778820611 | snp | C/T | 0.00156372 | 0.027918 | intron-variant | USP7 | GRCh38.p7 | 16:8923193 | ATCAAATTTGGCTTC[C/T]AGTAATGAAATACTG | 7874 |
rs778829620 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8953185 | TCTGTGAGGCCTCAC[C/G]TGAGGCTCCCCCTCC | 7874 |
rs778846826 | in-del | -/C | 3.31381e-05 | 0.00407037 | intron-variant | USP7 | GRCh38.p7 | 16:8921122 | CAACAAGCAGTAATG[-/C]ACCAATTGTTCAGAC | 7874 |
rs778847562 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8923078 | TGGATATTATACATA[C/T]ACCAGTGGGTTTTAA | 7874 |
rs778860852 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8921839 | CCACAAAAGGGCCTC[C/T]AGATCCAGGTTCAAA | 7874 |
rs778876441 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8896459 | ATGGCTCCAAAAGCC[A/G]TTTGTCCTCCAAGCG | 7874 |
rs778892813 | snp | G/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8899701 | ACGCGGTGGTAGAGA[G/T]CTCGGAAATACTCCT | 7874 |
rs778910587 | snp | G/T | 1.66222e-05 | 0.00288285 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8902426 | CATTGCTGGTCGTTT[G/T]GTTCCATTACTCCTT | 7874 |
rs778913414 | snp | A/C/T | 5.02309e-05 | 0.00501132 | intron-variant | USP7 | GRCh38.p7 | 16:8903226 | GAAGGAAGGTGGACG[A/C/T]TGGGAGCCACGGTGG | 7874 |
rs778915219 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP7, LOC105371074 | GRCh38.p7 | 16:8964572 | AGAATCACTTGAGGC[A/C]AAGAGTAAGAGACCA | 7874 |
rs778935990 | snp | A/G | 1.65957e-05 | 0.00288055 | intron-variant | USP7 | GRCh38.p7 | 16:8894686 | TATTTCTGTATATCA[A/G]CAAAACTCACATCTC | 7874 |
rs778951129 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8928663 | TGCTGGGTCTTTCAA[C/T]GGCAACCACAGTTCC | 7874 |
rs778997569 | snp | A/G | 1.64933e-05 | 0.00287165 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8910814 | TGCCACATAATCCAC[A/G]AATGATTCAAATACT | 7874 |
rs779006733 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8902125 | TCCACTAGCAGCCAG[C/T]TCGGGATCAACTGTT | 7874 |
rs779012705 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8959594 | TTGTAACTTTGCAAA[G/T]AATTATCTTAGCAAC | 7874 |
rs779040229 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8943726 | TCCTTCCCAAAGGCA[A/G]TATGTATTAAAATCA | 7874 |
rs779041197 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8927991 | CACTACAAACAATTA[C/G]CCACACATGGCGGTA | 7874 |
rs779042477 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8929985 | CAAGAAGGAGAGTAA[A/G]ACATGCTTGTTGTTC | 7874 |
rs779075201 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8926962 | ACTGTGCACTTTGTT[-/A]ACAGCAATTTTATCC | 7874 |
rs779111358 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8960900 | GGGCACTATTATTTG[G/T]CCACAGCCTCATGTG | 7874 |
rs779171215 | snp | C/T | 1.65427e-05 | 0.00287595 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8899161 | ACATTGGATCTGTGT[C/T]GAGCCTCTGTGCAAC | 7874 |
rs779175726 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8904190 | GTATCAGGAACTACT[A/C]TGGGACTGTGACCAA | 7874 |
rs779177713 | snp | A/C | 1.70417e-05 | 0.002919 | intron-variant | USP7 | GRCh38.p7 | 16:8921310 | CCTGTTTAAAAGAAT[A/C]ATCTGAGCCTTAGTT | 7874 |
rs779180174 | snp | C/T | 1.6517e-05 | 0.00287372 | intron-variant | USP7 | GRCh38.p7 | 16:8902226 | TTTAGAAGAGTCTAA[C/T]GGCTTAGGTGACAGA | 7874 |
rs779194801 | in-del | -/ACC | | | intron-variant | USP7 | GRCh38.p7 | 16:8959048 | GGCTGCAAAAGCCCT[-/ACC]ACCAAGGCAACACCA | 7874 |
rs779221710 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8932915 | AAAAAAACCAATGAA[A/G]GCCTATTAAATAAAT | 7874 |
rs779231502 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956601 | GAAACGCCATCTCTA[C/T]TAAAATATAAAAATT | 7874 |
rs779234594 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8902690 | GTCGGGAGTTCAAGA[C/G]CAGCCTGGCCAACAT | 7874 |
rs779242227 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8910336 | TACTCATTCTAAAGT[A/C]GTGATCCTCAGAAAA | 7874 |
rs779282422 | in-del | -/A | 1.65067e-05 | 0.00287282 | intron-variant | USP7 | GRCh38.p7 | 16:8899084 | CTGTGGAAAGCATGC[-/A]GTCAAGACCAAGCAA | 7874 |
rs779295073 | snp | A/T | 1.68485e-05 | 0.00290241 | intron-variant | USP7 | GRCh38.p7 | 16:8900976 | CTAATTATGGAAAAA[A/T]AAACCATCCAAACCT | 7874 |
rs779324002 | in-del | -/T | 2.77327e-05 | 0.00372365 | intron-variant | USP7 | GRCh38.p7 | 16:8902528 | AAAAACACGCTCATA[-/T]TTTAGTCCTCTATAT | 7874 |
rs779341524 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8911138 | GACAGCTTGGAATTG[A/G]GCAGTGTGGACAACC | 7874 |
rs779387106 | snp | A/G | 1.64768e-05 | 0.00287021 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8904483 | CTCCTTCCGCTTCTG[A/G]GCCTCGATCCTTTTC | 7874 |
rs779390981 | in-del | -/AAAAAA | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892608 | ACTAGTTAGAGGCTA[-/AAAAAA]AAAAAAAAAAAAAAA | 7874 |
rs779428609 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8931250 | CTGGAGTGCAGTGGC[A/G]CAATCTCAGCTCACT | 7874 |
rs779435090 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8907856 | AAATAAAATAACTAC[G/T]TGTAACTGGCATACA | 7874 |
rs779469319 | snp | A/C | 1.71381e-05 | 0.00292724 | intron-variant | USP7 | GRCh38.p7 | 16:8915554 | TTTTGGCTTTAAAAA[A/C]ACTTTTTTGTACTTA | 7874 |
rs779471790 | in-del | -/TG | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8958114 | AACAAAAAAGGAAAC[-/TG]AGATGGTCACCTTCA | 7874 |
rs779474136 | snp | A/C | 1.67125e-05 | 0.00289067 | intron-variant | USP7 | GRCh38.p7 | 16:8930260 | TCTGACAAGTTTCCG[A/C]CCACTGCGAGGCGGT | 7874 |
rs779497079 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8942551 | CAATATTTGGCTTAC[A/G]GCTTATTTATTTTTG | 7874 |
rs779526720 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8918113 | CCATTTCTTAACTTA[A/C]CATTACTTGTGAAAC | 7874 |
rs779593208 | in-del | -/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8896138 | GCCACCATGCCCAGC[-/T]TTTTTTTTTTTTTTT | 7874 |
rs779597376 | snp | A/C | 3.32132e-05 | 0.00407499 | intron-variant | USP7 | GRCh38.p7 | 16:8899558 | AAGAAAGAAATTTGT[A/C]TTTCTGGAGTGGGAT | 7874 |
rs779599421 | snp | C/G | 1.64749e-05 | 0.00287005 | intron-variant | USP7 | GRCh38.p7 | 16:8895002 | TCCAGGTTTTGACGT[C/G]AGCCACTCGGCCAAC | 7874 |
rs779654075 | in-del | -/AG | 5.29367e-05 | 0.00514447 | intron-variant | USP7 | GRCh38.p7 | 16:8930413 | CTTTAAAGAAGAAAA[-/AG]AAATTCCACGGGTTT | 7874 |
rs779661556 | in-del | -/TAT | | | intron-variant | USP7 | GRCh38.p7 | 16:8904992 | TAAAATAAAATAATC[-/TAT]TAACATGAAATTACT | 7874 |
rs779712034 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8948637 | GAAGTTCCACACGAT[C/G]GAATATTATTCTGCG | 7874 |
rs779716006 | snp | C/T | 1.65203e-05 | 0.002874 | intron-variant | USP7 | GRCh38.p7 | 16:8898499 | CGAGCCTTCTCTTTA[C/T]GACCCATAGTTACAT | 7874 |
rs779724746 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8950295 | AGAAGACACAACAGA[A/C]ATTTTCTGCTCTAAA | 7874 |
rs779735947 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8932898 | TACTAACTGAATAGG[-/A]AAAAAAAACCAATGA | 7874 |
rs779756366 | snp | A/G | 1.65255e-05 | 0.00287445 | intron-variant | USP7 | GRCh38.p7 | 16:8896953 | AGGTCAGCGTTAACT[A/G]CCACCCCTAACTGAA | 7874 |
rs779768839 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8955340 | GCCTCGACCTCCAAG[C/G]TTCAAGTGATCCTCC | 7874 |
rs779770564 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8912766 | TTGTCTCCAAATAAT[G/T]ATAATTAATTGATAA | 7874 |
rs779814646 | in-del | -/ACA | | | intron-variant | USP7 | GRCh38.p7 | 16:8931681 | AATAAGGTGTAAATT[-/ACA]ACAACATTCCAATCA | 7874 |
rs779846395 | snp | A/C | 1.64939e-05 | 0.0028717 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8900580 | ATCAAGGGCTTTATC[A/C]AGAGACACGTCATAG | 7874 |
rs779865840 | snp | C/T | 1.7849e-05 | 0.00298734 | intron-variant | USP7 | GRCh38.p7 | 16:8908499 | GCCTCTACTTACTCC[C/T]GGAAGCAATGAAAGC | 7874 |
rs779896241 | snp | A/C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8926408 | CGCTTGAACCTGGGA[A/C/G]GTGGAGGTTGCACTG | 7874 |
rs779899716 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8941572 | TTTGTCCACGCACGA[C/T]AGCAACATCAGAGTG | 7874 |
rs779936871 | snp | A/G | 1.73549e-05 | 0.0029457 | intron-variant | USP7 | GRCh38.p7 | 16:8930405 | ATCTCCCGCTTTAAA[A/G]AAGAAAAAGAAATTC | 7874 |
rs780011118 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8913700 | CGGAGGAGCATTGCA[A/G]GCTGTAAATATGTGG | 7874 |
rs780031919 | snp | C/T | 8.43604e-05 | 0.00649408 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8895735 | GTAGCTTACAATTTC[C/T]AGCAGCCTGAACAGA | 7874 |
rs780032891 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8897976 | GGAGCTGTCTACACT[A/G]GCAGCTTGGGGAGTA | 7874 |
rs780040314 | snp | A/C | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8899667 | ATTAGGGATTGTTTT[A/C]TCACAGAAAATGACA | 7874 |
rs780048050 | snp | A/C | 1.70307e-05 | 0.00291806 | intron-variant | USP7 | GRCh38.p7 | 16:8900483 | CTACAACTTAAAAAA[A/C]TCCTGAAATTAGTAC | 7874 |
rs780072846 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8954824 | AAATTAGCCGGTGCG[G/T]TGAGGGGCGCCTGTA | 7874 |
rs780075216 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8907352 | GACAGTTTCTGACCA[C/T]GGTAAAGACTGTGAA | 7874 |
rs780122464 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8910503 | GAAAGGACAAGATGC[C/T]TAAAACCCCACAAGA | 7874 |
rs780144462 | snp | A/C/T | 3.33808e-05 | 0.00408528 | intron-variant | USP7 | GRCh38.p7 | 16:8903414 | CTATCTGAAAATATG[A/C/T]ATGAAAGCACAGAAA | 7874 |
rs780192822 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8921876 | ACATACAGCACTTAA[G/T]CCAAAGAAAGTTAAG | 7874 |
rs780193845 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8928763 | TCACAAGAAGGGCAT[A/T]TCCACTTTCGGGTCC | 7874 |
rs780208880 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8955575 | GCCGGGCATGGCGGC[A/G]CGCCCCTGTAGTCCT | 7874 |
rs780209838 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8919960 | CATGTTAGTTGTCGG[C/T]GATGCTCACCTCTTC | 7874 |
rs780224987 | snp | C/G | 4.94458e-05 | 0.00497197 | intron-variant | USP7 | GRCh38.p7 | 16:8895154 | CAAAGGGATTTCCTG[C/G]GGACACGGACAACAG | 7874 |
rs780237390 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8951828 | TTGTTACTGAACACC[C/T]GATTCACAAAGGAAG | 7874 |
rs780242344 | snp | C/T | 1.65217e-05 | 0.00287412 | intron-variant | USP7 | GRCh38.p7 | 16:8916451 | AATAACTTCTGACCA[C/T]GCTTCAAAATATTCA | 7874 |
rs780248709 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8942681 | AGCTCTTGAGCAGCT[C/G]GGACTACAGGCGCAC | 7874 |
rs780262153 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8898515 | ACCCATAGTTACATT[-/A]AATTTGGACTCATAC | 7874 |
rs780286239 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8929661 | TGGCTGCTCCCTACT[C/G]ACAAGTGTGACTGTG | 7874 |
rs780310729 | snp | A/G | 9.94695e-05 | 0.00705159 | intron-variant | USP7 | GRCh38.p7 | 16:8899569 | TTGTCTTTCTGGAGT[A/G]GGATCTGAAGAGGAA | 7874 |
rs780351775 | in-del | -/T | 0.000544465 | 0.0164905 | intron-variant, frameshift-variant | USP7 | GRCh38.p7 | 16:8894528 | ACCCACACCAGCCCC[-/T]CGGGGGGGGGAGAAC | 7874 |
rs780372835 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8958417 | TAGAGAAGGCAGGAC[A/G]CCAAGTCCTTTTCAG | 7874 |
rs780394025 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8901811 | CCCTGCTCTTTAGGA[A/T]CTGACCAACGTGATT | 7874 |
rs780400836 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8892165 | CTAAGACTACAGCCA[A/C]CCCCCAGCCCAGAAC | 7874 |
rs780441128 | snp | A/C | 1.65666e-05 | 0.00287802 | intron-variant | USP7 | GRCh38.p7 | 16:8904586 | GGACAAAGGCATCCT[A/C]TTTGACCCCTGCAGA | 7874 |
rs780445193 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8943643 | TGGAGATGCCCACCA[C/G]TACTGAAGGTCTAGC | 7874 |
rs780450304 | snp | G/T | 1.65337e-05 | 0.00287517 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8898420 | CCTGTTCTCAAAGTC[G/T]GTGATTTTCATCTTA | 7874 |
rs780456579 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8957461 | CAAAAAACCATAAAC[A/G]GGCTGGGTGAGGTGG | 7874 |
rs780483368 | snp | C/T | 1.65485e-05 | 0.00287645 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8923255 | GGAGAAAGAATCCTA[C/T]GCTTTTTTGGTGTGG | 7874 |
rs780490651 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8902704 | ACCAGCCTGGCCAAC[A/G]TGGTGAACTCTCGTC | 7874 |
rs780499226 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8894916 | CCCAGGCCACGTCAC[C/G]TGGCAGCCGCCAAAA | 7874 |
rs780521213 | snp | C/T | 0.000263609 | 0.0114776 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8901198 | TTCAAGCTCCGCGTT[C/T]TGGGATCATACATCT | 7874 |
rs780522065 | snp | C/G | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956484 | AAGAACTGAATTTGG[C/G]CCAGGCGCAGTGGCC | 7874 |
rs780538173 | snp | C/G | 1.64898e-05 | 0.00287135 | intron-variant | USP7 | GRCh38.p7 | 16:8901101 | TAGCTGTAATGTACT[C/G]AGCAAAATCTACTCA | 7874 |
rs780548930 | in-del | -/AGAG | 0.000149019 | 0.0086306 | intron-variant | USP7 | GRCh38.p7 | 16:8910834 | ATTCAAATACTTTAA[-/AGAG]AGAGAGAGAAAAGTC | 7874 |
rs780557502 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8922446 | TGAGCCAAGATCAGG[C/T]CACTGCACTCCAGCC | 7874 |
rs780588278 | snp | C/G | 6.60131e-05 | 0.00574476 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8930354 | CACATTCCCATTGAT[C/G]ACAGGGTTCTGAGTA | 7874 |
rs780606881 | in-del | -/AA/AAA | | | intron-variant | USP7 | GRCh38.p7 | 16:8955705 | CACGATTCCATCTCA[-/AA/AAA]AAAAAAAAAAAAAAA | 7874 |
rs780607227 | snp | A/C | 1.64784e-05 | 0.00287035 | intron-variant | USP7 | GRCh38.p7 | 16:8905175 | AACAGAACAAAAGTG[A/C]ACACTACTCACTCAG | 7874 |
rs780663126 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8932653 | TCAGGTACTCTGAAA[C/T]GTCTTTCATCCACAT | 7874 |
rs780725184 | snp | C/T | 1.67716e-05 | 0.00289578 | intron-variant | USP7 | GRCh38.p7 | 16:8915228 | ATCATCAAAAGATCA[C/T]GCCATTAGATACACA | 7874 |
rs780730967 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8934173 | GCATGGATGCAAAAA[C/T]GAGGGCTCATTTTCT | 7874 |
rs780755061 | snp | A/C | 3.29544e-05 | 0.00405908 | intron-variant | USP7 | GRCh38.p7 | 16:8894980 | GCAACAGCGGCCACT[A/C]AAAGGCTCCAGGTTT | 7874 |
rs780760921 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8932061 | AGTGCCATGCTCACC[A/T]CCCCCTCCAAGAACT | 7874 |
rs780789987 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8951694 | CACCTGCACCCTGAG[-/A]CCCTCGCAGACAAGA | 7874 |
rs780798763 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP7, LOC105371074 | GRCh38.p7 | 16:8961054 | GATTCTGCTAAATTT[A/G]CAGATTAACTGTCCT | 7874 |
rs780840983 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8940664 | CACACTCCCTAAGAA[A/G]CTCCTGACCGCCATC | 7874 |
rs780900283 | snp | C/T | 1.64969e-05 | 0.00287196 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8900593 | TCAAGAGACACGTCA[C/T]AGTCCTGAATTCTCT | 7874 |
rs780907194 | snp | A/C/G/T | 0.000119261 | 0.00772134 | intron-variant, missense | USP7 | GRCh38.p7 | 16:8894532 | CACACCAGCCCCCGG[A/C/G/T]GGGGGGAGAACCCTT | 7874 |
rs780911831 | snp | C/T | 1.64806e-05 | 0.00287054 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8903319 | CGAGGAGTTCTTCAA[C/T]ACTTTGAACACAGTG | 7874 |
rs780918666 | snp | A/G | 2.25884e-05 | 0.00336061 | intron-variant | USP7 | GRCh38.p7 | 16:8906618 | AGAAATTCAGTATTA[A/G]TTTACACAAAAAATA | 7874 |
rs780953557 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8912955 | AGAGCAACAGAAACC[A/G]CAGCACAAAACCCAG | 7874 |
rs780964757 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8908022 | TCAAAATTAAATTTA[C/T]TAGAAATCCTGTGAA | 7874 |
rs781077969 | snp | A/T | 1.65004e-05 | 0.00287227 | missense, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8906487 | TGATTATCTCCACTA[A/T]GAACCAGGACTGCAT | 7874 |
rs781103191 | snp | C/G | 1.64773e-05 | 0.00287026 | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893979 | CACCGTCCTCGCCTT[C/G]AACACACCAGCTTGG | 7874 |
rs781116127 | snp | C/G | 1.65031e-05 | 0.00287251 | intron-variant, utr-variant-3-prime | USP7 | GRCh38.p7 | 16:8894156 | GCAGCCCTGGAACCC[C/G]TCAGCGGGGTGGTGG | 7874 |
rs781139433 | snp | A/G | 3.31011e-05 | 0.0040681 | intron-variant | USP7 | GRCh38.p7 | 16:8904579 | ACCTGCAGGACAAAG[A/G]CATCCTCTTTGACCC | 7874 |
rs781188940 | snp | C/T | 4.24007e-05 | 0.00460419 | utr-variant-5-prime, intron-variant | USP7 | GRCh38.p7 | 16:8936721 | CCTCAGCATTCTTTT[C/T]TATTTTTTAAAGCAT | 7874 |
rs781194088 | snp | A/G | 3.29891e-05 | 0.00406122 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8895677 | TCGTTGCAGGAGATA[A/G]ACATTCTAATAGTTC | 7874 |
rs781201356 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892367 | GGCACACACACTGCA[A/G]TGGAAGTTGAGAAAG | 7874 |
rs781219672 | snp | C/G | 4.94222e-05 | 0.00497078 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8897064 | TTCTAACAGGTCCCG[C/G]ACACACCCATGCTTG | 7874 |
rs781227260 | snp | C/G/T | 0.000124799 | 0.00789845 | intron-variant | USP7 | GRCh38.p7 | 16:8923430 | TGCAAAAAAAACACA[C/G/T]CATCAGTCACAGAGC | 7874 |
rs781235560 | in-del | -/C | 0.000233758 | 0.0108085 | intron-variant, frameshift-variant | USP7 | GRCh38.p7 | 16:8894535 | CCAGCCCCCGGGGGG[-/C]GGGAGAACCCTTACC | 7874 |
rs781247345 | snp | G/T | 3.29468e-05 | 0.00405861 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8919036 | ATCCATTTACCTTTC[G/T]TAGCTGATTCGTGAA | 7874 |
rs781250168 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8912177 | GAACCAGTGCAGTGG[C/T]TCAGTGGCTCACGCC | 7874 |
rs781264408 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8901903 | CTCCGGGCCTCACAG[A/G]AAACTCGCAGCCAAG | 7874 |
rs781305301 | snp | A/G | | | utr-variant-5-prime, intron-variant | USP7 | GRCh38.p7 | 16:8956357 | TCAAACATTCATGAA[A/G]TTAAAGCTCCTGGCA | 7874 |
rs781307481 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8945971 | CCATAATCAAGACAG[A/C]ACTGCTGGCAAAGGA | 7874 |
rs781376756 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8905200 | ACTCAGTTTTGATTC[C/T]CTGATGTAGACTAAC | 7874 |
rs781378052 | snp | C/T | 0.000181415 | 0.00952232 | synonymous-codon, intron-variant | USP7 | GRCh38.p7 | 16:8904555 | GTCGGTGACCGCCTG[C/T]AAAACTTCACCTGCA | 7874 |
rs781385492 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8893495 | AATGCACACAATGAA[-/G]GGGAAGAGCGCTATT | 7874 |
rs781414004 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8943711 | TTCTAGAGTCAACTG[C/T]CCTTCCCAAAGGCAA | 7874 |
rs781416334 | snp | C/T | 4.95495e-05 | 0.00497718 | intron-variant | USP7 | GRCh38.p7 | 16:8895601 | GCAGCAGATGGGGCT[C/T]ATGAATTCTCTCTGG | 7874 |
rs781422551 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8899685 | ACAGAAAATGACATC[A/G]ACGCGGTGGTAGAGA | 7874 |
rs781426456 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8921762 | CATCGACGAATTCAC[A/G]ATGAGGCACAAAATT | 7874 |
rs781451960 | in-del | -/TCAA | | | intron-variant | USP7 | GRCh38.p7 | 16:8920185 | ACATATAGAAACTGC[-/TCAA]TCAATCTGTTAAACG | 7874 |
rs781494085 | snp | A/C/T | 8.25572e-05 | 0.00642437 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8921232 | AATACGACGACTGAA[A/C/T]GACTTTTCATCATCT | 7874 |
rs781530149 | snp | A/G | 1.65288e-05 | 0.00287474 | intron-variant | USP7 | GRCh38.p7 | 16:8916606 | CTCAACTTTCAAATG[A/G]GCAAATTAAAAGTAA | 7874 |
rs781530613 | snp | A/G | 0.000185822 | 0.00963724 | intron-variant | USP7 | GRCh38.p7 | 16:8929590 | TGGACATGCTTTTTG[A/G]CAGAACATGGTTTCA | 7874 |
rs781531752 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | USP7, LOC101929989 | GRCh38.p7 | 16:8892285 | AAGGAGGGAAGGGCC[A/G]GGTCCGCGGGGACCC | 7874 |
rs781594829 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8935652 | AATTACCATCCCATA[A/G]TACGCATATCCCACT | 7874 |
rs781624087 | snp | A/C | 1.65075e-05 | 0.00287289 | intron-variant | USP7 | GRCh38.p7 | 16:8916476 | TATTCATTGTAAGAA[A/C]TATACAAGTATTGCT | 7874 |
rs781647989 | snp | A/G | 1.65853e-05 | 0.00287964 | intron-variant | USP7 | GRCh38.p7 | 16:8921108 | AAAAGTTAAGGGAAC[A/G]ACAAGCAGTAATGCA | 7874 |
rs781649234 | snp | G/T | 1.81612e-05 | 0.00301335 | intron-variant | USP7 | GRCh38.p7 | 16:8898672 | ATATAAATAAATGAC[G/T]TGTTTATTTGCCTAA | 7874 |
rs781651186 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8903199 | AGGCAATCAGTATTT[C/T]CTAGTGACACGGAAG | 7874 |
rs781748798 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8926447 | TCATGGCATTGCACT[C/T]CAGCCTGGGCAACAA | 7874 |
rs781766616 | snp | C/T | 3.29462e-05 | 0.00405857 | synonymous-codon, nc-transcript-variant | USP7 | GRCh38.p7 | 16:8905308 | AGTACACCTTGACAC[C/T]ACGTCGTCATCAAAT | 7874 |
rs781777567 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8925594 | TGGTGAGACTCAGAA[C/T]TGAAGTTTGCACTTG | 7874 |
rs796070785 | in-del | -/AG | | | intron-variant | USP7 | GRCh38.p7 | 16:8913338 | TCCAGCCTGGGCAAC[-/AG]AGCGAGACTCCCTCT | 7874 |
rs796078108 | in-del | -/AA | | | intron-variant | USP7 | GRCh38.p7 | 16:8903868 | GTGAAACTCTGTCTC[-/AA]AAAAAAAAAAAAAGG | 7874 |
rs796119885 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8949299 | TTAACATCGTGGCAC[A/G]TTCCACTGGGATTGA | 7874 |
rs796151972 | in-del | -/GG | | | intron-variant, frameshift-variant | USP7 | GRCh38.p7 | 16:8894530 | CCCACACCAGCCCCC[-/GG]GGGGGGGAGAACCCT | 7874 |
rs796210141 | in-del | -/CC | | | intron-variant, frameshift-variant | USP7 | GRCh38.p7 | 16:8894525 | TGAAACCCACACCAG[-/CC]CCCGGGGGGGGGAGA | 7874 |
rs796233337 | in-del | -/AAA | | | intron-variant | USP7 | GRCh38.p7 | 16:8901321 | ACAAACAAAAAAACG[-/AAA]AAAAAAAAACAGTAA | 7874 |
rs796308576 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8916650 | CCTAAACTGGATAAT[C/G]AGCTATTATTCTCAA | 7874 |
rs796319585 | snp | A/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8944331 | CCTGGAGTCAGGAGG[A/C]GGCCAGAGTCCTGGA | 7874 |
rs796330607 | in-del | -/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8895856 | TTTTTTTTTTTTTTT[-/T]GAGACAGTCTCAATC | 7874 |
rs796360379 | in-del | -/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8895959 | CTCCCACCTCAGCCT[-/C]CCGAGTAGTTGGGAC | 7874 |
rs796376076 | in-del | -/A | | | intron-variant | USP7 | GRCh38.p7 | 16:8944244 | GTGCAAAAAAAAAAA[-/A]GCACAGCCAAAATAC | 7874 |
rs796405383 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8926645 | GTACACTGGATCCTA[C/T]GTATTATTTTTTTGC | 7874 |
rs796436296 | snp | A/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8928675 | CAACGGCAACCACAG[A/T]TCCAAACCAAGGAAA | 7874 |
rs796478379 | snp | C/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8925521 | GTGCTTTTGGAACTT[C/T]CACCCTATACATTAA | 7874 |
rs796577239 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8937604 | ACTTGGGAGGCTGAG[A/G]TGGGACGTAAAGGCT | 7874 |
rs796612388 | multinucleotide-polymorphism | AAC/CAA | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956770 | TCGTATTAAAAAAAC[AAC/CAA]AACAAAAAAAAAAAA | 7874 |
rs796660862 | in-del | CTTTAAAAT/GAAGCAAGGAGA | | | intron-variant, upstream-variant-2KB | USP7 | GRCh38.p7 | 16:8951258 | TATATATATTTAATC[CTTTAAAAT/GAAGCAAGGAGA]TGGCCTCTTAAGTCA | 7874 |
rs796682869 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8913351 | ACAGAGCGAGACTCC[C/G]TCTCAAAAAGAGGAG | 7874 |
rs796722594 | snp | C/T | | | downstream-variant-500B, nc-transcript-variant | USP7, LOC101929989 | GRCh38.p7 | 16:8892092 | GGAAACATTACAACA[C/T]GTTCTTTGGAAAAAG | 7874 |
rs796726972 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8956635 | CGGGCATGGTAGCGT[A/G]TGCCTGTAGTCCAGC | 7874 |
rs796735855 | snp | C/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8951959 | TTTCTATATTCAAAG[C/G]ATGTGGGGAACCACA | 7874 |
rs796764405 | in-del | AA/C | | | intron-variant | USP7 | GRCh38.p7 | 16:8955719 | AAAAAAAAAAAAAAA[AA/C]AAAAACATTGCACAG | 7874 |
rs796798403 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8936905 | GCTGTGACAAATCTG[A/G]TTTAAAACACTGTAT | 7874 |
rs796801010 | in-del | -/AAAGTT | | | intron-variant | USP7 | GRCh38.p7 | 16:8927337 | AAAAAAAAAAGAAAG[-/AAAGTT]AAAGAAAAACAGAAT | 7874 |
rs796926343 | multinucleotide-polymorphism | CTG/GTA | | | upstream-variant-2KB, intron-variant | USP7 | GRCh38.p7 | 16:8938304 | ACTTTGAGATAACTG[CTG/GTA]ATTCACACACAGTCT | 7874 |
rs796956782 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8918608 | TGGGGTCAGGAGTTC[A/G]AGACCAGCCTGGACA | 7874 |
rs796963919 | snp | G/T | | | intron-variant | USP7 | GRCh38.p7 | 16:8896375 | CTCGCTTACTCTTAT[G/T]AGGTAATAGATTAGG | 7874 |
rs796981687 | in-del | -/AG | | | intron-variant | USP7 | GRCh38.p7 | 16:8916986 | AAAAAAAAAAAAAAA[-/AG]AGGAAGCAGAATGGC | 7874 |
rs796991836 | snp | A/G | | | intron-variant | USP7 | GRCh38.p7 | 16:8919018 | CTGCAGGAGAGGAAC[A/G]CTATCCATTTACCTT | 7874 |
rs797004731 | in-del | -/TT | | | intron-variant | USP7 | GRCh38.p7 | 16:8935202 | GAGCTAAGGCACTAA[-/TT]TTTTTTTTTTTTTTT | 7874 |