SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs147247156 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP40 | GRCh38.p7 | 2:233479855 | GGGACAGTGCTGTCC[A/G]GAAAGCAGCCCAGAC | 55230 |
rs147298663 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233549411 | TTAATTGATCTAATG[A/G]CCAGTCACACTACAC | 55230 |
rs147315077 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233554328 | TCATACAAGTTGACT[C/T]GTACTAACTACAAAG | 55230 |
rs147337728 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476683 | CCTTCTGATCACAGA[G/T]CACCCAGGATAAGCT | 55230 |
rs147418697 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233532550 | CTTCCACACTGTGGA[A/G]TGTACTTTTGTTTTC | 55230 |
rs147508130 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | USP40 | GRCh38.p7 | 2:233508774 | GAAAAAAAATGCTTT[A/C]TTTTTTACCTTTATG | 55230 |
rs147524544 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233513227 | AGCTTCCAATATCTA[C/G]AGTCTCTTGAGTGAC | 55230 |
rs147580474 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | USP40 | GRCh38.p7 | 2:233502789 | AGCTGAAGAACTGGC[A/G]TAGGGATCATGCTAC | 55230 |
rs147589565 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP40 | GRCh38.p7 | 2:233545810 | ACACTACCTGGCTAC[A/G]ATTAGAATATTTGGG | 55230 |
rs147620283 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP40 | GRCh38.p7 | 2:233485061 | TATTCCTAGTTTGCT[C/G]TAAGTTCTTTTTTAA | 55230 |
rs147624581 | snp | A/C/G | 0.00557542 | 0.0525036 | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233566162 | TCACTGGGGAGGGAG[A/C/G]GGGGAAGGGGAGCGG | 55230 |
rs147682196 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233481863 | GGTTGTTTTCCACAC[C/G]CATGTTATTTCCGTA | 55230 |
rs147686397 | snp | C/T | 0.000150978 | 0.00868712 | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233561236 | AAAGTTCATATGGAA[C/T]CAAAAAAGAGCCCGC | 55230 |
rs147726503 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP40 | GRCh38.p7 | 2:233545444 | CAATTGGGTGCTGTC[A/G]TGGAGCCTTCTTTGC | 55230 |
rs147755952 | in-del | -/AACA | 0.0486741 | 0.148216 | intron-variant | USP40 | GRCh38.p7 | 2:233510241 | GGCCCATGAAACTTT[-/AACA]AAAAATCTCAATTTA | 55230 |
rs147788403 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233541711 | ATGAAAGAAGACCTC[A/G]CATCTTTAAAACAGC | 55230 |
rs147794100 | in-del | -/T | 0.0592355 | 0.161582 | intron-variant | USP40 | GRCh38.p7 | 2:233511979 | TCAATTTCCATACTC[-/T]TAAGATATTGTCTTC | 55230 |
rs147830805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233524973 | AAGTGAGATAATTAA[C/T]ATAAAACACCTATTA | 55230 |
rs147893876 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233520101 | GTATACTATCAGCCC[A/G]AGTGCACTATTTAAA | 55230 |
rs147937625 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | USP40 | GRCh38.p7 | 2:233505877 | CAAAAAAAGAAAACT[A/C]TAGGCCAATATCCCT | 55230 |
rs147953945 | in-del | -/TAAA | 0.0396786 | 0.135148 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485648 | GAAAATCAAACATCT[-/TAAA]TAAGCAAAACTCAAC | 55230 |
rs147999667 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | USP40 | GRCh38.p7 | 2:233531877 | AAAATCTTACTAGGC[C/T]TCATGCCTGTAATCC | 55230 |
rs148019660 | in-del | -/T | 0.305186 | 0.243833 | intron-variant | USP40 | GRCh38.p7 | 2:233494273 | AACAACAAAATTCCA[-/T]TTTTTTTTTTCACCT | 55230 |
rs148056001 | in-del | -/T | 0.0652144 | 0.168387 | intron-variant | USP40 | GRCh38.p7 | 2:233516183 | ATATGTCTACCTGTA[-/T]TGCCAATATACACTG | 55230 |
rs148095295 | snp | A/G | 0.00310614 | 0.0392864 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233521057 | GCATAAATTTTTAAC[A/G]TGGAGCCAGTCAATC | 55230 |
rs148099692 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | USP40 | GRCh38.p7 | 2:233553467 | AGTAAAGCACAGAGA[C/G]AGACCTCACATCAGT | 55230 |
rs148116537 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP40 | GRCh38.p7 | 2:233507869 | AGAAATGCTAAGTGC[A/G]TGAGGTAATGAGTAT | 55230 |
rs148132025 | in-del | -/A | 0.0275645 | 0.114116 | intron-variant | USP40 | GRCh38.p7 | 2:233488143 | TACTTAGAAGCAGTG[-/A]AAAAAATGCTACACT | 55230 |
rs148158811 | snp | C/T | 0.0111196 | 0.0737302 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233566794 | AAGTGATTTATGGAT[C/T]GTGGACTATGCTTCC | 55230 |
rs148210542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233492013 | GTCTTAAGGAAATTA[C/T]AGGCTGACACTACCG | 55230 |
rs148265580 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233498906 | ACAAAAATACTGACA[G/T]GAAACAGAATGCACT | 55230 |
rs148276043 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233542527 | CCAGCCTGGGCAACA[C/T]AGAGAGACCAGCACA | 55230 |
rs148308434 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233481960 | ACAGCGCAGGGTCTG[C/T]GGGGTTCGTGCTGGG | 55230 |
rs148369854 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233525900 | AATTTTTACTCAAAA[C/G]AGCAAGACTAATTTG | 55230 |
rs148415910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233523848 | ACCCCCACTCCCCAA[C/T]TCAGTATAGATTCTC | 55230 |
rs148528765 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | USP40 | GRCh38.p7 | 2:233494030 | TAGCTAGTTCTTCCC[A/G]CCTCATTTTTTGTTA | 55230 |
rs148571324 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | USP40 | GRCh38.p7 | 2:233480384 | GGGGGAGGATGAGGA[C/T]GCCTGGGGGCCTCTG | 55230 |
rs148571610 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP40 | GRCh38.p7 | 2:233558523 | ACGAGACCACCTATT[A/G]GATCACTCCATTTCT | 55230 |
rs148579502 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | USP40 | GRCh38.p7 | 2:233502037 | GTACATCGAATGTTG[A/G]TGATAGAGCAAGTAA | 55230 |
rs148589760 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233545092 | AGCAAGAAGCCTACA[C/G]TCCACAATACTAAAA | 55230 |
rs148622085 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233483775 | AAAACCCGAAAAAAC[C/G/T]TGAAATCTGAGACAG | 55230 |
rs148739924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233534393 | CCTCCCCATCCACTA[C/T]GCCCCTATCCTCTCA | 55230 |
rs148845945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233497542 | GAAGAATGAAAGATA[A/G]GGAGGATATTTTACT | 55230 |
rs148854398 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | USP40 | GRCh38.p7 | 2:233509781 | GGGAGGCAGAGGTTG[C/T]AGTGAGCTGAGATCA | 55230 |
rs148866333 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233560358 | TTTCTCCTGGCTCCA[A/C]GTGAGTTCCTGCCTT | 55230 |
rs148909338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233515758 | TAATACAAAAACCTT[C/T]CCTTATGATAAAGTA | 55230 |
rs148910750 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | USP40 | GRCh38.p7 | 2:233547395 | TCCAAATACAACTGA[C/T]AGAATGTCAGAAATA | 55230 |
rs148968964 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | USP40 | GRCh38.p7 | 2:233491439 | GCAGGGACATGTTGT[C/T]GGCAGACTCCCAAGA | 55230 |
rs149036534 | in-del | -/AAAG | 0.0652144 | 0.168387 | intron-variant | USP40 | GRCh38.p7 | 2:233533087 | AAGAATCAGGAAAAT[-/AAAG]GAGAAGATATAAAAA | 55230 |
rs149056098 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | USP40 | GRCh38.p7 | 2:233536908 | TTTTTCTTTTGGAGA[C/G]AGGGTCTCATCCTGT | 55230 |
rs149065816 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233550754 | GGCTTACAAAGTAGG[C/T]TGATTTTGTAATTAA | 55230 |
rs149073906 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233519785 | TAATTACCTGACATT[G/T]AGTAGTTTTTGCCCA | 55230 |
rs149233597 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | USP40 | GRCh38.p7 | 2:233488108 | ATTTCTAGCACACAC[A/T]CTGTTTCAAGTTGCT | 55230 |
rs149298598 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | USP40 | GRCh38.p7 | 2:233538721 | AGGGATATTAGCAGA[A/G]ATAAAGACAAGCATT | 55230 |
rs149321887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233503655 | CACTGTCAGCCAAGA[A/G]TATCATATCCAGCAA | 55230 |
rs149384339 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | USP40 | GRCh38.p7 | 2:233553107 | TAGAGACAGCACATC[C/G]AGGCCACAGGAAATG | 55230 |
rs149392665 | snp | A/C | 0.00223327 | 0.0333414 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523348 | CTGTGAGGACAGTGC[A/C]CACTTCTGCATTAGC | 55230 |
rs149439044 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | USP40 | GRCh38.p7 | 2:233480114 | CCATGGTCACGAGGT[C/T]ACGCTCACCTGCCCT | 55230 |
rs149507350 | in-del | -/GGAA | 0.0298908 | 0.118541 | intron-variant | USP40 | GRCh38.p7 | 2:233506817 | TTCGGAGGCTGAGAT[-/GGAA]GGATCACTTGAGCCC | 55230 |
rs149535795 | snp | C/T | 0.00222582 | 0.0332859 | intron-variant | USP40 | GRCh38.p7 | 2:233542256 | ACAAATACATACACA[C/T]ACATACTATACCTCT | 55230 |
rs149596782 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | USP40 | GRCh38.p7 | 2:233512108 | AAAGCCAGATAATCC[A/G]AATCAATCCATAAAT | 55230 |
rs149605168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233563961 | TTTCTACTTCGAGTT[A/G]TCCTTTAACTTCAAC | 55230 |
rs149704174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233554919 | TCTAATGTAAACTCC[A/G]TTTCTTTATTTTCTT | 55230 |
rs149710238 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233493771 | GACTAAATATCCCTT[A/G]CTTAAAGGTATCTTA | 55230 |
rs149716926 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP40 | GRCh38.p7 | 2:233556239 | GTGATAATTGACTAT[A/G]TAAGATTTGTAGGGC | 55230 |
rs149754156 | snp | C/T | 0.000351132 | 0.0132455 | intron-variant | USP40 | GRCh38.p7 | 2:233481166 | GAGTCAGAGAGGGCT[C/T]TGTCAGCTGCACATC | 55230 |
rs149755973 | snp | C/T | 7.33837e-05 | 0.00605694 | intron-variant | USP40 | GRCh38.p7 | 2:233559806 | TAAAGAGCTGATCCT[C/T]GTACCTCATTACTGG | 55230 |
rs149766507 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP40 | GRCh38.p7 | 2:233528967 | TTTCCCCCAAGATCA[A/G]CATTGCATTCAATAG | 55230 |
rs149772094 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233545041 | CCTCAAATTACTCCC[A/G]TAAATCAAGTTCTTA | 55230 |
rs149868256 | in-del | -/G | 0.00953873 | 0.0683987 | intron-variant | USP40 | GRCh38.p7 | 2:233541437 | CCATGTGAGGACACA[-/G]GGAAGAAGACGGCCA | 55230 |
rs149913131 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233514337 | GACTGTGTGGTCAGG[A/G]ATGAAAGGAGAAGGA | 55230 |
rs149925867 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233565880 | CAGTTAGTGTACAGG[C/G]TTTGGCCCACAATAA | 55230 |
rs149976191 | snp | C/T | 0.00101982 | 0.0225582 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233489445 | GAGGTGGGCTGGGGA[C/T]GGGACACCGAACTCC | 55230 |
rs149984727 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | USP40 | GRCh38.p7 | 2:233504997 | ACAAGACAGAGATCA[C/T]ATCAAGTATTTTTTC | 55230 |
rs150036288 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | USP40 | GRCh38.p7 | 2:233509297 | TCTGTTTTCCAATAC[G/T]AAAGGTCTCAGTTCT | 55230 |
rs150092585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233546876 | GAAGGTATAACAACA[C/T]GATAAGGATTGGCTC | 55230 |
rs150143006 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475444 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 55230 |
rs150151167 | in-del | -/TCGAGTT | 0.0130921 | 0.0798413 | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233566412 | CTCGAGGCTAGACTC[-/TCGAGTT]GTGTTTTTTTAGTTT | 55230 |
rs150230333 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP40 | GRCh38.p7 | 2:233485294 | AGAATTTTCCATGTA[C/T]GGTCAGAAGTGAAAC | 55230 |
rs150231735 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | USP40 | GRCh38.p7 | 2:233516604 | GAGGCAGGAGAATGG[C/T]GTGAACCCGGGAAGC | 55230 |
rs150239174 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | USP40 | GRCh38.p7 | 2:233536606 | CAGTGAGCTGAGATT[A/G]TGCCACTTCACTTCA | 55230 |
rs150268550 | in-del | -/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233508585 | GTCTGAGTGTTGCTC[-/T]TTTTTGGGGCTAGCA | 55230 |
rs150283007 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233521615 | GTAGAGTATCTTGTT[A/C]TAACATTTTCCCACA | 55230 |
rs150299419 | snp | A/G | 0.0980852 | 0.198549 | intron-variant | USP40 | GRCh38.p7 | 2:233506733 | GACACTGCCTCTACC[A/G]AAAATACAAAAAAAA | 55230 |
rs150354636 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP40 | GRCh38.p7 | 2:233511658 | GGTACTAGTTATAAT[C/T]CTGGTTATGGAAGGG | 55230 |
rs150417088 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | USP40 | GRCh38.p7 | 2:233556236 | TCAGTGATAATTGAC[C/T]ATATAAGATTTGTAG | 55230 |
rs150447839 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233496016 | TTCAGCAAACAAATA[A/T]GTGTAATGTTTTTCT | 55230 |
rs150469641 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233563793 | ACAAGCAGTGCACAT[C/T]GTGCACTAAGATGTC | 55230 |
rs150496301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233482119 | CAGTGCCCCGCCTCT[A/G]CTAGGAACATGTCGT | 55230 |
rs150548224 | snp | C/T | 0.00155048 | 0.0277999 | intron-variant, synonymous-codon | USP40 | GRCh38.p7 | 2:233487947 | GTCCGAACACACTGA[C/T]AACAGCTGCGGGTGG | 55230 |
rs150560176 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233538398 | AACACAGGCAAAGTC[A/G]TTTTCTTGAAAAGTT | 55230 |
rs150621483 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233507993 | AATAGTTTCAGATTT[G/T]GGAGCATTTTGGATT | 55230 |
rs150646999 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | USP40 | GRCh38.p7 | 2:233536568 | AGGCTGGAGGACTGC[-/T]TGAGCCTGGGAGGCA | 55230 |
rs150672609 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233513717 | TTATGCTTATTAAAT[C/T]GGCCAGCATGTGCTA | 55230 |
rs150733643 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | USP40 | GRCh38.p7 | 2:233558826 | GTTAATCGGATTAAC[G/T]CCAAATACCAGCCCT | 55230 |
rs150767740 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | USP40 | GRCh38.p7 | 2:233499203 | TGTGTTATTCCCCTC[C/T]CTGTGTCCATGTGTT | 55230 |
rs150789319 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233565161 | CATTATTGTCATCAC[C/T]CAGGATATATTTAAG | 55230 |
rs150820002 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | USP40 | GRCh38.p7 | 2:233504649 | ATAAAGGGATTCAAT[A/G]AGAGGATATAACAAT | 55230 |
rs150830142 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | USP40 | GRCh38.p7 | 2:233548654 | TAACTATTAGACAAC[A/G]GTATTATATCAATGT | 55230 |
rs150881606 | snp | G/T | 0.0217236 | 0.101931 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477228 | GTTGCAGAGCTAAGT[G/T]ACTACATGCACTGGC | 55230 |
rs150886343 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | USP40 | GRCh38.p7 | 2:233554784 | AAGATACAATAAAAT[A/C]TGTTTTATGAGGAAA | 55230 |
rs150937363 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233481117 | ATCAACAAGAGTTTC[C/T]GGTCCCTCTCAGTTT | 55230 |
rs150999888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233523991 | GATCTAGCATCTGAC[A/G]CACAACCTGGTATAA | 55230 |
rs151052079 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP40 | GRCh38.p7 | 2:233528455 | GAATGAGGCTTATCA[C/T]GCAACTCACGTACTT | 55230 |
rs151086865 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | USP40 | GRCh38.p7 | 2:233502489 | TGTCATGTCAAAGGG[C/T]CAAAAAGTGCTCAAA | 55230 |
rs151116271 | in-del | -/ACT | 0.0283406 | 0.115616 | intron-variant | USP40 | GRCh38.p7 | 2:233510977 | ATCAGCTTGTCATGC[-/ACT]ACTATTTGCTACGGT | 55230 |
rs151142665 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | USP40 | GRCh38.p7 | 2:233506310 | CATGCAGAATAATGA[C/G]ACTAGATTCCCTAAC | 55230 |
rs151152774 | snp | A/G | 0.0208675 | 0.0999914 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551400 | AAAGGGCTTGAGATT[A/G]ATCCGGAGAGGGAAT | 55230 |
rs151209527 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233484222 | GTACGAATTTATGCT[A/C]TTAATTTTATTTAAT | 55230 |
rs151247309 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233535151 | AGAGGCGAGATCCCA[A/C]GAAGGAGCCCCAATT | 55230 |
rs151264366 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | USP40 | GRCh38.p7 | 2:233489298 | GACTGATTCCTCCTC[C/T]ATCCCTCACACCAGC | 55230 |
rs151298905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233541101 | TTAAACAAGAATTTT[A/G]GAAGAGATACGTAAG | 55230 |
rs151306455 | in-del | -/TC | | | intron-variant | USP40 | GRCh38.p7 | 2:233491635 | GTGTGTGTGTGTGTG[-/TC]TGTCTGTCTGTGTGC | 55230 |
rs180783996 | snp | A/T | 0.0162398 | 0.0886349 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233568557 | ATATAAGATTATATT[A/T]ATATAATCTTATATC | 55230 |
rs180796613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233528936 | CCATCTCTTTAAGTA[A/G]GAATCCATCATAGGC | 55230 |
rs180802547 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233510913 | TTCAGTTCCTCATAG[A/C]CCTGCTTTTCCTTTC | 55230 |
rs180805624 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233548671 | TATTATATCAATGTT[A/G]GAAGTTCCTTATTTT | 55230 |
rs180840213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233493264 | AAATGGCACAGTGTT[A/G]TTATTATGTGATGTC | 55230 |
rs180855488 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476082 | ACACGTGTGCAGAAG[C/T]GACGTGGCTTCTGTC | 55230 |
rs180861782 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233515978 | GGCACCTTTGTTGAA[A/G]GTCAATGACTACGCA | 55230 |
rs180877892 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233484168 | GTCTCAACAACAACA[A/G]CAAAAGAAAATCTTA | 55230 |
rs180885467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233479413 | ACTAAAAATACAAAA[A/G]TTAGCTGGGCATAGT | 55230 |
rs180911304 | snp | A/T | 0.00349169 | 0.0416372 | intron-variant | USP40 | GRCh38.p7 | 2:233498637 | AGTCAAAATTGGGAT[A/T]AAAAAAATTCAAAGT | 55230 |
rs180920717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233532779 | AGACCCTGTCTCTAA[A/G]AAAATGAAAAAATTA | 55230 |
rs181016959 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233565101 | CGTTGTACTTTAAAT[G/T]ACAGGAATTAAAAAA | 55230 |
rs181053062 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233553649 | CAGTAGTTGCCTCTC[A/C]TTTCTCCTCTTATCA | 55230 |
rs181059253 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233525889 | GTCAGCCTAGGAATT[G/T]TTACTCAAAAGAGCA | 55230 |
rs181067782 | snp | A/G | 1.68105e-05 | 0.00289914 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556870 | CTGCCTCTCGCTAAC[A/G]TTCTTACATTCTTTA | 55230 |
rs181073115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233538744 | CAAGCATTTCTGGTG[C/T]GGTGGCTCATGCCTA | 55230 |
rs181075075 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233546387 | GATAAACCTGAAGAT[A/G]AAATTGCAAACAGAT | 55230 |
rs181099008 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233501978 | TGGAGTTGTGGTCTT[C/T]TGGAGCCCAGTGACA | 55230 |
rs181099235 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233519472 | AAAAACAAACATATG[A/G]CAAAATGTTAATATT | 55230 |
rs181141489 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233511141 | CTGCACTGTAATAAG[C/G]TGATTAGCTGGGTAT | 55230 |
rs181151402 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP40 | GRCh38.p7 | 2:233549493 | CGTTACTTTTATGTA[C/T]TTTGGCTAAGATCAT | 55230 |
rs181159709 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233529186 | TTCTCTACTCTTGTT[A/G]GGCTTCGATCCCTAC | 55230 |
rs181164964 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476734 | GACGTGCAGCGGCTG[C/T]CCTTGCTTAGCAGAG | 55230 |
rs181283003 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | USP40 | GRCh38.p7 | 2:233484728 | GCTCAAGTGATCCAC[C/G]CATCTCAGCCTCCCA | 55230 |
rs181479665 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543347 | AAACAAATAAAAACA[G/T]CTTAAACACACCATG | 55230 |
rs181488881 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP40 | GRCh38.p7 | 2:233533254 | AAATGTAATGATGAT[C/T]TTACATTATTACAGG | 55230 |
rs181490656 | snp | C/T | 0 | 0 | intron-variant | USP40 | GRCh38.p7 | 2:233498986 | GCTCCAGGTGGTATA[C/T]ATCTTAGCGTTCTTT | 55230 |
rs181497031 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233516736 | GGTGGCAGGTGCCTG[G/T]AACCCAGATATTCGG | 55230 |
rs181497276 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562811 | TAGAGCTTCTAAAGA[A/T]AAAGGTAGAATCAGA | 55230 |
rs181513536 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233480162 | CCTCTCTTCCCCAGA[C/T]GCCCCCAGTGGCAGA | 55230 |
rs181620315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233492556 | AGCATTAGTTAACAT[A/G]AACTACTGTAACCCA | 55230 |
rs181631505 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233475587 | AGCTTTCTCAATCCC[C/T]AAATTAAAAAAACAG | 55230 |
rs181688279 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | USP40 | GRCh38.p7 | 2:233506824 | GCTGAGATGGAAGGA[G/T]CACTTGAGCCCTGGG | 55230 |
rs181692459 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233539191 | GAGATTTAAAAATTC[C/T]TCAGTAATTAATAGA | 55230 |
rs181714558 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233557594 | CCAAACCAAGGGGCA[C/T]ACCAAGACTGAGAAG | 55230 |
rs181734030 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233521212 | ACTAATTAGAGGTGA[C/T]CAAGTTCTACTGAGT | 55230 |
rs181739126 | snp | A/G | 0.000612618 | 0.017491 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485727 | CCTCATTGCTATGCC[A/G]GTAAGCCCCAATTTC | 55230 |
rs181742613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233548424 | GTTATCTAAATCAAT[A/G]CTCATTTTATTTTTC | 55230 |
rs181753983 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP40 | GRCh38.p7 | 2:233510699 | GTGAGCCACCGCGCC[C/T]GGCCAACATACACTA | 55230 |
rs181805247 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233524861 | TGGTCCCAACTCCAC[C/T]GATATGTCCATAACA | 55230 |
rs181815448 | snp | C/T | 0.00174658 | 0.0294998 | intron-variant | USP40 | GRCh38.p7 | 2:233489319 | TCACACCAGCCAGTG[C/T]GTCAGCAGCAGAGAG | 55230 |
rs181831424 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233515716 | TAGGCTTTTCTTCCA[C/T]GGTTTGTGCTTTTTG | 55230 |
rs181839798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233532570 | CTTTTGTTTTCCATA[C/T]ATCTCTGCTTTTGGT | 55230 |
rs181840255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233490187 | TTTTTTTTTTGAGAC[A/G]GAGTCTCACTCTGTC | 55230 |
rs181881808 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233502205 | CACTTTTGAAAAGTT[C/T]TGTGGTTTCTTTCCT | 55230 |
rs181927336 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233527942 | TTCCATGTCATCTAT[C/T]ATCCTTATTTCCACT | 55230 |
rs181935809 | snp | G/T | 0.0399052 | 0.1355 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233567812 | TAACCTTATATAAGA[G/T]TATAGTTATATAACC | 55230 |
rs181965001 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233525642 | GTTACTGTGCCAACT[C/G/T]ACATATGAAGATGAC | 55230 |
rs181968664 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233563751 | ATACCTCCCTGTCAG[A/T]CACCATCAGGATTCA | 55230 |
rs182003105 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233498228 | GGGCCAAAACTTCAG[A/C]GTGTATCTATAAAAT | 55230 |
rs182135497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233513516 | GTGATGAATTGTGCC[C/T]TGAAGAGCTGGCAGT | 55230 |
rs182261273 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233546270 | CAAAAGAGATGTCCA[A/G]GAAACCACAACCCAA | 55230 |
rs182269406 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233507339 | ATGTGTCCAAAGGGT[A/G]TGAAATCAGTGTGTC | 55230 |
rs182299908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233490688 | CTCCTTCTCTGTGAA[C/T]GTTAATGCATAAGAA | 55230 |
rs182469214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233539335 | AGTGAACACAGAACA[C/T]TGAGCAGGATAGACA | 55230 |
rs182477232 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233507586 | CACAGAAAGGCTGAT[C/T]GGTAATATGACCTCA | 55230 |
rs182488083 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | USP40 | GRCh38.p7 | 2:233479368 | AAGAGATTGAGACCA[G/T]CCTGGCCAACATGGT | 55230 |
rs182508718 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233503069 | CTGAAGAGAAATTCA[A/C]AACAATGATCTTAAG | 55230 |
rs182511239 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477336 | ATGCCCAGGAAACCC[A/T]CGTTTGTGGCATCAG | 55230 |
rs182522711 | snp | C/T | 0.000132494 | 0.00813815 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523265 | TTCCTTGGGGATGGC[C/T]GTCCAACCCTCCCCA | 55230 |
rs182531405 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233559569 | AAAATCAGCTCTTGT[A/C]CTTCTCCCCGTTTTT | 55230 |
rs182538598 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233539914 | ATGGCCAGGCAGATC[A/G]CTTGAGTCCAGGAGT | 55230 |
rs182538805 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486525 | GCAGAAAGAACAACA[C/T]TCAGCAAGGCAGGAG | 55230 |
rs182549528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233503661 | CAGCCAAGAATATCA[C/T]ATCCAGCAAAGCTAT | 55230 |
rs182741103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233522153 | TCTACAAATCTCAAG[A/G]TTGGGCAGGGGTAAT | 55230 |
rs182741449 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | USP40 | GRCh38.p7 | 2:233555718 | TCAGGTCACTGCAAC[C/T]TCCACCTCCCGGGTT | 55230 |
rs182744414 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233565660 | TGGGAGTCGATTCTG[C/T]TGTTTCTTAGAACAC | 55230 |
rs182746755 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233558794 | TACAGTGTTTTTTTT[G/T]TTTGTTTGTTTTTGT | 55230 |
rs182750256 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233517962 | TGTTCTCACTGATAC[A/G]TGGGAGCTAAGCTAT | 55230 |
rs182753260 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | USP40 | GRCh38.p7 | 2:233556064 | GAACTTGCAGTGAGC[C/T]GAGATCGTGCCACTG | 55230 |
rs182754699 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233497027 | TGTGGGGCATAAGCT[C/G]TAAGTCTGACAGAAG | 55230 |
rs182759862 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | USP40 | GRCh38.p7 | 2:233517257 | AGCCACTATGGAAAA[C/T]AGTGTGGAGATTCCT | 55230 |
rs182762428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233535667 | TGTTAGAATGCAATG[C/T]AAAGCTCTTCAGAGA | 55230 |
rs182766091 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233482398 | TCAATTTCTTTCCAC[A/T]TCATTCTATTACCTG | 55230 |
rs182777433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486136 | GCAAACTCTTATTCC[A/G]CATTTCAATTTCCTT | 55230 |
rs182892201 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476968 | CACTGTGAGAAGCCG[A/G]TCAGGGCGAACGAGA | 55230 |
rs182952078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233500473 | TAGTAATTAAAACAA[C/T]TTCTTGAGGGAAAAA | 55230 |
rs183005718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233534857 | TTTTAAGCCTCAAAC[A/G]TCAGTGCAGTCTAGT | 55230 |
rs183026127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233499797 | CTATAAATTTTTTTT[C/T]CCTACAACCCTGGAG | 55230 |
rs183038477 | snp | G/T | 5.40132e-05 | 0.00519651 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233512566 | GTTATCAAAAAGATT[G/T]ACCTGGACAAAGAAG | 55230 |
rs183056340 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233496017 | TCAGCAAACAAATAT[A/G]TGTAATGTTTTTCTT | 55230 |
rs183058167 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | USP40 | GRCh38.p7 | 2:233529904 | CTCCCAGGTTCAAGC[A/C]ATTCTCGTGCCTCAG | 55230 |
rs183087720 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233508946 | AGTGGGCTCCTCAAT[A/C]TCTTTGATGATTCCA | 55230 |
rs183090760 | snp | C/T | 1.71843e-05 | 0.00293119 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533700 | AAATCAGACTCAGCC[C/T]GGAGAGAACTATTCT | 55230 |
rs183094144 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233491503 | ACTTTTCCACATTCT[C/G]TCCTTCCTCAAAGAG | 55230 |
rs183126490 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | USP40 | GRCh38.p7 | 2:233516884 | AAAAAAAAAGAATAT[C/T]GTGTTGTCTGATTTG | 55230 |
rs183154649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233560454 | CTTTAAGTATTTAAA[A/G]GAGAATAAGCATTTA | 55230 |
rs183332284 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP40 | GRCh38.p7 | 2:233507931 | ACATATATGTACCAG[A/G]ATATTAAAATGTACC | 55230 |
rs183338207 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233546797 | TTTAAGGCGGAGTGA[C/G]AAGGCCACTTTCTTA | 55230 |
rs183353886 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233550438 | TATTTATTTGGTTAC[A/G]TCAATAATAGCCTCA | 55230 |
rs183355889 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233530745 | GGAATCTTCTTTTTG[C/T]AAATTGCTTATTTAT | 55230 |
rs183549796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233488439 | GAACACCCAAACTTT[C/T]GGAAAAGGGGAAAAA | 55230 |
rs183588493 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233523792 | TGAAGTGCTCCTGGC[C/T]GCCTTCTAGAGATAG | 55230 |
rs183588918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233526631 | ACACAAAAAAGCTAA[C/T]ATTTTCTATCTCCCT | 55230 |
rs183596687 | snp | C/T | 0.00351264 | 0.041761 | intron-variant | USP40 | GRCh38.p7 | 2:233491021 | GGCGTGTATTGCCTG[C/T]GGGTACTTACCACTG | 55230 |
rs183600222 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233549969 | TTAGATTAAGAGATA[C/T]TTTAAAGATGTTTAT | 55230 |
rs183680275 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP40 | GRCh38.p7 | 2:233526817 | ACTTCAAAATGGGGC[C/T]AATGTGTCTTCATGA | 55230 |
rs183714089 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | USP40 | GRCh38.p7 | 2:233499358 | TCCTTTCTATGGCTG[A/C]ACAGTATTCCATGGT | 55230 |
rs183737895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233547751 | AAGACATTAAAGGGA[C/T]TTTAGAAAATGAAAA | 55230 |
rs183752976 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233566747 | CCCGCCCCAACTGGG[A/C]GCCGCCATGTTGGCG | 55230 |
rs183759649 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP40 | GRCh38.p7 | 2:233484333 | TGCCTTCCAAGAACA[C/T]GACGTGGCTCTAACA | 55230 |
rs183765813 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233527017 | AAATACTGTTCTATA[C/T]TACAGGGTATAAAGT | 55230 |
rs183767282 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233492027 | ACAGGCTGACACTAC[C/T]GGAAAGATAATTTTA | 55230 |
rs183770639 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233509467 | TCATTTTTTTCTTTT[A/G]ATCAATTTCTGCACA | 55230 |
rs183814658 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP40 | GRCh38.p7 | 2:233489014 | AGGAAATGACCCAAA[C/T]CTGCTCTTTAAGTTC | 55230 |
rs183814659 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233524254 | CCTGCCTCAGCCTCC[C/T]AAGTCACTGGGATTA | 55230 |
rs183821817 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233506175 | AAGCACCAGAATAAA[C/G]AGCCCAGAAATAAAT | 55230 |
rs183823551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233504545 | GTAAAAGGTCATTAT[A/G]ATTGATAATGGTCAT | 55230 |
rs183825562 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233540429 | TTTAGGGGATGAACT[C/T]TGACATTTTTTAGGA | 55230 |
rs183866739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233547055 | AAGCCAGAATGGGAG[C/T]TCCATTCACTGCAGT | 55230 |
rs183914469 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233481454 | AAAATCCTCTTGCTC[A/G]ATGAAAACAAACTCG | 55230 |
rs183975936 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233542634 | AGTAGGCCGTGATTG[C/T]GCCACTGCACTCCAG | 55230 |
rs183983803 | snp | A/G | 0.00662273 | 0.0571621 | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233561255 | AAAAGAGCCCGCATC[A/G]CCAAGTCAATCCTAA | 55230 |
rs184450697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233556703 | TCTGGATTATAGGCT[C/T]ATGATTTAGGTGTAG | 55230 |
rs184459468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233483319 | ACACGGCATAACCCC[A/G]TCTCTACCAAAAATA | 55230 |
rs184499969 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233519117 | GGCTTGGAATACAGA[G/T]GGGTACAGGGATATT | 55230 |
rs184557535 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233531047 | ATTTAAGTGATTTGT[A/T]TAACAAAGAAAAATG | 55230 |
rs184575302 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP40 | GRCh38.p7 | 2:233497517 | CAGTTTGGAGGCTGA[A/G]AGGAAACATGAAGAA | 55230 |
rs184618092 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | USP40 | GRCh38.p7 | 2:233538511 | TAAGTTCATATTCTA[C/T]AGTCACTAAACGGAT | 55230 |
rs184622326 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233501352 | AACCAGATCACATAG[C/G]CCCTTGTGCAGACAT | 55230 |
rs184656148 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233532374 | CCTTTGTAACTTCAC[G/T]TCAGCCTCTGGTTGG | 55230 |
rs184665627 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | USP40 | GRCh38.p7 | 2:233515574 | AAGGGTTTTTTTTTT[C/T]CTTTAATATTCTGAA | 55230 |
rs184669325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233552835 | AATCAATGCTCATTT[C/T]ATTTGCTGGAAAAAT | 55230 |
rs184669854 | snp | A/G | 0.031825 | 0.122064 | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475149 | GGAAAAAGGGCCACA[A/G]ACGTTCCTTATTTTA | 55230 |
rs184684295 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233497840 | AAACAGCAAAGAGCA[A/T]TCCAGGGCAAGGCCC | 55230 |
rs184698180 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233479287 | TGTGGAAACAGAGCC[A/G]GGCGCGGTGGCTCAC | 55230 |
rs184703439 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233550779 | AATTAATTTGTTTTC[A/C]AAACCTTTTCTTTCC | 55230 |
rs184720176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233514764 | TTTTAATGGACTTTA[C/T]TGAGTTATAATTTTC | 55230 |
rs184723452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233477957 | CACTCAAGAGACTGG[C/T]TTTCGCTGTGACCCC | 55230 |
rs184725651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233492901 | CCCATCGTGATGTGT[A/G]CGGCTGAGTGCTGAG | 55230 |
rs184734977 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233510707 | CCGCGCCCGGCCAAC[A/G]TACACTATTTCTTCT | 55230 |
rs184739623 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | USP40 | GRCh38.p7 | 2:233537799 | CAATTCTGAACTTCA[A/G]GAAATGCTAAAGGAA | 55230 |
rs184784894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233505531 | ATACAAAGGATCATA[A/G]GAGACTATTATGAAC | 55230 |
rs184829336 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233548129 | GAGAAAAATTGATTA[A/C]TCAATAAATAGAAAT | 55230 |
rs184864825 | snp | C/G | 0.0023933 | 0.0345097 | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475339 | AGATAATTTTTTGTA[C/G]TTTTAGGAGAGACAG | 55230 |
rs184897506 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | USP40 | GRCh38.p7 | 2:233528110 | CAGCCTCCTGAGTAG[C/G]TGGGATTACATGTGT | 55230 |
rs184900157 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | USP40 | GRCh38.p7 | 2:233556409 | ACATAAGCACACATA[C/T]ATAAATGAACTTTCT | 55230 |
rs184941441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233527368 | CTAGCTGGAGATGGT[A/G]CTCGATGTCTGAATT | 55230 |
rs184946919 | snp | C/T | 0.0379877 | 0.132479 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233567349 | CCTTATATAAGATTA[C/T]AGCTATATAACCTTA | 55230 |
rs184978405 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP40 | GRCh38.p7 | 2:233553346 | GAAGATAAAATGGGA[A/G]AAAAACCCACAAAAC | 55230 |
rs184982413 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233492323 | AATCACTCTACCGTG[A/T]TCACATAATGATGAA | 55230 |
rs184985339 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233532682 | CTCATGACCCTCTAC[C/T]GATGACACCAGCATT | 55230 |
rs185177860 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233534626 | AACAAACAGAAGAGT[A/G]TAGGGCATAACCCAA | 55230 |
rs185201629 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233568738 | ACACCCCTTCCTGCA[C/T]GTCACTATAAGATGC | 55230 |
rs185276476 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | USP40 | GRCh38.p7 | 2:233479473 | GAGACTGAGGCAGGA[C/G]AATCGCTTGAACCCG | 55230 |
rs185292257 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233563161 | TGTTGCAGTTTTCCT[A/G]CCACATGTAAGGCTA | 55230 |
rs185378894 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233500560 | AGAGCAAAAGAGAGC[A/T]AAAATAAGGAAGTCA | 55230 |
rs185384237 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543652 | TGCCATGTGAGGACA[A/C]AGCAAGAAAGAGTCA | 55230 |
rs185418765 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233503337 | GGGGAGAATAAATGA[A/C]AAAAGACACAGCGTA | 55230 |
rs185420125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233510917 | GTTCCTCATAGCCCT[A/G]CTTTTCCTTTCTAAC | 55230 |
rs185423186 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233549369 | AGATGAATTCAAGTA[A/T]TTGGCTTTAAATTTA | 55230 |
rs185433476 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | USP40 | GRCh38.p7 | 2:233529058 | ACATGCCAGTTCGCT[A/C]CAACTACTTACCTAT | 55230 |
rs185435976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486239 | GGAACTTCCTCAGTG[C/T]GGGAGAAAAGGAAAG | 55230 |
rs185489150 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233518524 | GTGAGCGGAGATCGT[A/G]TCACTGCACTCCAGC | 55230 |
rs185498712 | snp | A/G | 0.000233969 | 0.0108134 | intron-variant | USP40 | GRCh38.p7 | 2:233557052 | TTTAGATGTAATTCC[A/G]GGCTTCAGATTTTTT | 55230 |
rs185510372 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233539002 | CTCCTACGCTTCAGT[C/G]TGAGTGACAGAGCAA | 55230 |
rs185513250 | snp | A/G | 0.00597247 | 0.0543191 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233568498 | TAAGATTATAGTTAT[A/G]TAATCTTATAAATAT | 55230 |
rs185519207 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233483699 | AAACTCAATGGAGCA[A/T]TTCAGATTTCAAATT | 55230 |
rs185536232 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233484730 | TCAAGTGATCCACCC[A/T]TCTCAGCCTCCCAAA | 55230 |
rs185540375 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233519898 | TGATGTTAATTGGAA[C/G]AGAAAGGACACCTAC | 55230 |
rs185544524 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233502029 | GTCATCAGGTACATC[A/G]AATGTTGGTGATAGA | 55230 |
rs185610940 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | USP40 | GRCh38.p7 | 2:233515885 | TAAAGCTTGAGGTTC[A/C]TTTCTGCACATACAA | 55230 |
rs185613403 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233541707 | ATAAATGAAAGAAGA[C/T]CTCACATCTTTAAAA | 55230 |
rs185629075 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP40 | GRCh38.p7 | 2:233479390 | CAACATGGTGAAACC[C/T]CGTCTCTACTAAAAA | 55230 |
rs185638267 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233565115 | TTACAGGAATTAAAA[A/G]AGAAATATATTGCTT | 55230 |
rs185658189 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233526374 | CTAGGTTCAGATTCC[C/T]ACATCTGCCTGTATC | 55230 |
rs185666220 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233507643 | AAAAAAGAGTTGACA[A/T]CGTAGAAGCAGAGAG | 55230 |
rs185670655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233546579 | GACTGAAGAGAGACA[C/T]GGCAATATTGAAAAA | 55230 |
rs185682807 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233548639 | GGTGGAATCTGAACA[A/T]AACTATTAGACAACA | 55230 |
rs185738105 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233560779 | TTCCAGAGTACCAAA[C/T]TGAAAGAATACTAGC | 55230 |
rs185742730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233554303 | CTTCAAGTATATCCT[C/T]GAGACTTTTTCATAC | 55230 |
rs185753459 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233533337 | TTTCATTTGGCATAA[C/T]ATAGTTCTTGTTAGC | 55230 |
rs185770823 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233498397 | TTTATCAAAAAACTA[C/T]AGTAAGAAAAAAGTA | 55230 |
rs185782820 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP40 | GRCh38.p7 | 2:233524014 | TGGTATAACGGAGGC[A/G]CTCAAGAAATGTCTC | 55230 |
rs185837756 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233522437 | GTACTACGAAAGAAA[C/T]GGTCCACAAGTGCTC | 55230 |
rs185841893 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233558889 | TGTATTATACCCCAT[G/T]TTGCTTGAAAGTCCA | 55230 |
rs185963089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233539421 | GAGTATGTTCTCAAA[A/G]TACAATGAAATTAAT | 55230 |
rs185983524 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233499122 | AAGCCCAGAATGTAT[C/T]AGCAATTTTTCCTGA | 55230 |
rs185985560 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | USP40 | GRCh38.p7 | 2:233516749 | TGTAACCCAGATATT[C/T]GGGAGGCTGAGGCAA | 55230 |
rs185998924 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP40 | GRCh38.p7 | 2:233481050 | AGGAGAGGAAAGAAC[A/G]CAGGGGGCGGAGAAG | 55230 |
rs186231861 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476206 | GCGCCTGACTCCAGC[A/G]GTGTCCTTTCTGCCC | 55230 |
rs186232365 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233558049 | TGAAGAGCAGCAGAT[A/G]AAGTGGATGAAAGCT | 55230 |
rs186275827 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233554725 | AACTATAATTTAGCT[A/T]AAAATCTATCAGAAA | 55230 |
rs186294574 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233475761 | GCAAAGCTTTTCAGC[A/G]ATTTCATTAATATTT | 55230 |
rs186338897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233498862 | TAGATTTATTTTTTT[C/T]ATTCATTTTACATTC | 55230 |
rs186340173 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233532908 | CACTCCAGCCTGGAC[A/G]AGAGAGTGAGGCTGC | 55230 |
rs186356494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233549658 | CCCTTTTTTTATTGA[C/T]ATATATCTAGTTGAA | 55230 |
rs186374306 | snp | C/T | 0.000127024 | 0.00796844 | intron-variant | USP40 | GRCh38.p7 | 2:233511666 | TTATAATTCTGGTTA[C/T]GGAAGGGTTGATTTT | 55230 |
rs186398289 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476751 | CTTGCTTAGCAGAGC[A/G]ACTCACCCTCGGAGG | 55230 |
rs186461398 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233525668 | ATGACACAGAGAGCA[A/G]GCAAATGAATACTCT | 55230 |
rs186476642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233490450 | GTGCTGGGATTATAG[A/G]CATGAGCCACCACAC | 55230 |
rs186484468 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233507493 | GGTACTATTCAGCCA[C/T]AAAAAAGAATAAAAT | 55230 |
rs186491140 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP40 | GRCh38.p7 | 2:233553815 | AGCTCTCACATGGCA[A/G]AAGATATCAGTTGCT | 55230 |
rs186514758 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233516032 | CCACTGTAAATATTT[G/T]AGGCTTCACGGGCCA | 55230 |
rs186522390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233490859 | GGGATAAAGTGAATG[C/T]TTTACAAATGTTCCA | 55230 |
rs186527762 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | USP40 | GRCh38.p7 | 2:233550500 | TAATTCAAACAACAA[A/C]AAAAAAAACCCCAAA | 55230 |
rs186540292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233530976 | AGATCAAATATTTAT[A/G]TTTTACACATTTTAC | 55230 |
rs186596454 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233494983 | ATATATATATATACA[A/C]ACACATAAAAAATAA | 55230 |
rs186606579 | snp | A/G | 0.000443066 | 0.0148774 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233529483 | CATTCAGTAAATGAC[A/G]TGGAACCCCATATCT | 55230 |
rs186883118 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233525314 | TGGATACATTAAAAC[A/G]TGGATATTTTATTTC | 55230 |
rs186919331 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233547754 | ACATTAAAGGGACTT[C/T]AGAAAATGAAAATGT | 55230 |
rs186922630 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233527139 | TTATTTTCTAAAAAA[A/G]AGACAACTTTATACT | 55230 |
rs186925275 | snp | A/G | 0.000157549 | 0.00887409 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233489405 | AAAGCCTGCCTGGGC[A/G]CTTCCTCTCCACCGT | 55230 |
rs186935219 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233567004 | TATAAGATTATAGCT[A/G]TATGATCTTATATAA | 55230 |
rs187103034 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233506925 | AAAAAAAAATCTAAC[A/G]AAGAGTTAATATCCG | 55230 |
rs187119742 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP40 | GRCh38.p7 | 2:233500460 | AATAAAACAAAAATA[A/G]TAATTAAAACAATTT | 55230 |
rs187129282 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233482591 | ACTGGAGTTTTTTTT[G/T]TTTGTTTTTTTTTTT | 55230 |
rs187147270 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233539265 | ACACAATCAATTTGA[A/C]CTAGTTGTCACTTGT | 55230 |
rs187163626 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | USP40 | GRCh38.p7 | 2:233502476 | TATTTTCTTTGAGTG[C/T]CATGTCAAAGGGTCA | 55230 |
rs187188983 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233478146 | ATCTGGCCATGGTGA[A/G/T]TGAAGCTGCCTTGTA | 55230 |
rs187190778 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | USP40 | GRCh38.p7 | 2:233540080 | CAGTGAGCTGAGGTC[A/G]TGCCGCTGCACTCCA | 55230 |
rs187198401 | snp | C/T | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486947 | GCTGCTGGAGAGAAA[C/T]AGGAGGGACTAGAGG | 55230 |
rs187204240 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233503977 | CTATTAGTGGCTAAG[A/G]ACACAATAAAGATGT | 55230 |
rs187217700 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233517060 | TCTTAATTTTGATGT[C/T]GATTTTGTTGTTGTT | 55230 |
rs187231023 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP40 | GRCh38.p7 | 2:233546287 | AAACCACAACCCAAA[A/G]GAAATTCAAGGAAGA | 55230 |
rs187335304 | snp | A/G | 0.000769083 | 0.0195946 | intron-variant | USP40 | GRCh38.p7 | 2:233559963 | CTAAATGAATTCTTT[A/G]AGTGTTGACTAAGGC | 55230 |
rs187375353 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233521336 | CTACATAATTTGTTG[A/C]CACATTTTTCACAGA | 55230 |
rs187378374 | snp | C/T | 0.000165256 | 0.00908849 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485874 | TCTGCCTCAGGGAGC[C/T]GGCAGTCCCACCCTG | 55230 |
rs187398669 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP40 | GRCh38.p7 | 2:233518028 | TTGGGGACTTGGGGG[A/G]AAGGGTGGGAGGGGG | 55230 |
rs187404563 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233534476 | TACTTTATATAGAAA[A/T]TTACTTGGGAGTTAA | 55230 |
rs187405269 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP40 | GRCh38.p7 | 2:233556094 | GCACTCCAGCCTGGG[C/T]GACAAAGCAAGACTC | 55230 |
rs187409053 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233537030 | CTGGGATTACATGTG[C/T]GCACCACCGCATCCA | 55230 |
rs187411350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233483418 | ATCGCTTGAGCCCGT[A/G]AGGCAGAGGTTACAG | 55230 |
rs187417230 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233500514 | TAAATCTTGGACAAG[C/T]GAGCAAATACAATTT | 55230 |
rs187432961 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP40 | GRCh38.p7 | 2:233564259 | TAAATGTGGTGGCAG[C/T]AGGGAAGAGGAACAT | 55230 |
rs187455658 | snp | C/T | 0.000764994 | 0.0195426 | intron-variant | USP40 | GRCh38.p7 | 2:233561125 | AAAATTTTCTGAATA[C/T]GCTAAAACACCCCAG | 55230 |
rs187517365 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233497131 | TAAAAAGATGGGTTG[A/G]ATTTGGAAAGCTAGA | 55230 |
rs187694284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233550045 | AGGGCTCTAAAACTA[C/T]ATGATATAAGCTCTC | 55230 |
rs187729049 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233530111 | GGCCTCAGATTTTCA[C/T]CTTGATTACAAATAC | 55230 |
rs187733524 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233496419 | TTTATAAAAACAAAA[C/T]GTTAAAAACACGGTA | 55230 |
rs187737371 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233513055 | TAATTTAAAATACTA[G/T]AATCTTTGAGAATTA | 55230 |
rs187744367 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477083 | TGCGGTTCACGCACA[C/T]GTTGTGCATTTTCTG | 55230 |
rs187758838 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233509142 | GCTGCTACCAGGTTG[G/T]TCACTCTTTCCAACC | 55230 |
rs187760529 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477346 | AACCCACGTTTGTGG[C/T]ATCAGCCGGAGAGTT | 55230 |
rs187763474 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233514288 | GAAGGAAAAGTACAG[C/G]GTGTTAGGAGAGTAC | 55230 |
rs187769303 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233491578 | TCCTGTTTCCTCATC[A/G]TAACACTCATCCCAA | 55230 |
rs187773469 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233526938 | GAAAAATGACTTGGA[A/G]ACTACAGCACTGTTT | 55230 |
rs187907474 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | USP40 | GRCh38.p7 | 2:233535527 | AGCCCTACTGTAAGA[A/G]GAAGGACCATGACCC | 55230 |
rs187928348 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233509588 | GCTCATGCCTGTAAT[A/C]CCAGCACTTTGGGAG | 55230 |
rs187935345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233547288 | CACAAAATTTAGGCA[C/T]AGATCATCTCCCTGG | 55230 |
rs187994025 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233514912 | TCAATTTGCAGCCAA[C/T]CCCTCTTCCTCCCTC | 55230 |
rs188017441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233488573 | CTCTGTTCAGCCGGG[A/G]TTAAGATTCTCATGC | 55230 |
rs188021208 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233524034 | AGAAATGTCTCCTTG[C/G]CGTACAACTAGCACT | 55230 |
rs188024918 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233505574 | ATAAATTTAAAAACA[A/T]AGAAGAAATGGATAA | 55230 |
rs188097458 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233553612 | TGAAAATAACACCAG[A/G]GAGGTGTTCCACTAA | 55230 |
rs188174756 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233551217 | GCTAAACACCCTAAT[C/G]CATGAGACAGTCTCC | 55230 |
rs188200684 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP40 | GRCh38.p7 | 2:233517446 | CTGGAGAGCAGTGGC[A/G]CGATCTCGGCTCACT | 55230 |
rs188207951 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233492114 | ACCACACATGTGATG[G/T]GATCCTATAAGATTA | 55230 |
rs188225648 | snp | C/T | 0.00795532 | 0.062565 | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233565694 | ACTACTGTTTCTATG[C/T]ACAGTAGTTGGGTTT | 55230 |
rs188264559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233497593 | AGATACCTGGCAAGG[C/T]TGGAACGAGAAGCCA | 55230 |
rs188274214 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233526774 | ACCACAGGCAAGACA[C/T]TGAGTCTCTTTAAAT | 55230 |
rs188443660 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233531218 | ACTGCTCTTTTTCAA[C/T]GATCTGTCTACCTTT | 55230 |
rs188466700 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP40 | GRCh38.p7 | 2:233501413 | TGGGAAACCACAGGA[A/G]GGTTGTGAGTATAGG | 55230 |
rs188469667 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233519189 | GGTTATAGAACTCTA[C/T]ACATTTACTGATGAT | 55230 |
rs188483870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233484703 | GTCCAGGCTGGTCTC[A/G]AACTCCTGGGCTCAA | 55230 |
rs188487360 | snp | A/G | 0.000455695 | 0.0150877 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233491240 | AGGAGAGAAACTTGC[A/G]CAGGCTCGTTCCCAG | 55230 |
rs188542974 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233508151 | AATATTTATTATGCA[A/T]CTCTAAAAGATATTT | 55230 |
rs188552836 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233547019 | ACAAGCATTTGAGAG[A/C]AATGCTTGTACAGCT | 55230 |
rs188696302 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543127 | GAACATGTCAAAATT[A/C]CCCGGTAAGTTATTT | 55230 |
rs188713683 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233561703 | CAATGGCAACCAAAG[A/C]CAAAATTGACAAATG | 55230 |
rs188717971 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP40 | GRCh38.p7 | 2:233504683 | AAATATATATGCAAA[C/T]ACCACCAGAACACCC | 55230 |
rs188718238 | snp | C/T | 0.0037712 | 0.0432594 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233540736 | TCAAAAGTTTCTGGC[C/T]CAGCTGATCAACAGG | 55230 |
rs188718745 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233506804 | CGATCCCAGCTACTT[C/T]GGAGGCTGAGATGGA | 55230 |
rs188732866 | snp | A/G | 0.000151308 | 0.0086966 | intron-variant | USP40 | GRCh38.p7 | 2:233524567 | CAGTTCATCCCCTAG[A/G]AAGAGATCACCAGTG | 55230 |
rs188748890 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP40 | GRCh38.p7 | 2:233539127 | CATGAAGCAAAAACT[A/G]TCAAAACTTTTTTTT | 55230 |
rs188763695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233557572 | TGTGCTTAAGAAAAA[C/T]TTATAACCAAACCAA | 55230 |
rs188784524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233520637 | ACAAAACCAAAACAT[A/G]TGTATACTTGGCTTA | 55230 |
rs188792469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233502050 | TGGTGATAGAGCAAG[C/T]AACATGAAGAGTAAA | 55230 |
rs188817274 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233481845 | CCTTTCCCAGGACTC[C/G]CAGGTTGTTTTCCAC | 55230 |
rs188942179 | snp | C/T | 0.00835141 | 0.0640778 | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475437 | CCAAAGTGCTGGGAT[C/T]ACAGGCGTGAGCCAC | 55230 |
rs189003460 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233523898 | GGCACTATGCACAGA[A/C]CCCCTACTCCAGCAC | 55230 |
rs189011410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233487725 | TTATTTAATAAATAA[C/T]TATTGACTATGACAT | 55230 |
rs189018915 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233532692 | TCTACCGATGACACC[A/G]GCATTTTGGGAGGCT | 55230 |
rs189034357 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP40 | GRCh38.p7 | 2:233498491 | AATGGGTACCTTGTA[C/T]GAAAATATGACATAA | 55230 |
rs189104322 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | USP40 | GRCh38.p7 | 2:233499588 | GGAGTTGCCACACTG[C/T]CTTCCACAATGGTTG | 55230 |
rs189252815 | snp | A/C | 0.0166325 | 0.0896639 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233566726 | CCAAAACGCGAAGCG[A/C]ACGAACCCGCCCCAA | 55230 |
rs189287835 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP40 | GRCh38.p7 | 2:233515942 | TTGAAAAAATGCTAT[C/G]TCTCTGCATGAAAAT | 55230 |
rs189294129 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233542189 | AATTAAACCGCATAC[A/C]TTCTTACATATATAC | 55230 |
rs189311932 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP40 | GRCh38.p7 | 2:233479391 | AACATGGTGAAACCT[C/T]GTCTCTACTAAAAAT | 55230 |
rs189370673 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233532521 | TCTGGGCCCTTGAGC[A/T]GCTGCTCAGGCTGCT | 55230 |
rs189376873 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233515668 | CAAATGCTTTTTGAA[C/G]AGTAGAAGTTTAAAA | 55230 |
rs189382635 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233552945 | GACAATGTTCAGTAA[A/C]CCACTGAGTGAACTG | 55230 |
rs189398784 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233498171 | AGTAAGAAATTCTGC[C/T]ACCATTACCTTACAG | 55230 |
rs189414644 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP40 | GRCh38.p7 | 2:233479292 | AAACAGAGCCAGGCG[C/T]GGTGGCTCACGCCTG | 55230 |
rs189485806 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233538632 | TAAACAAGATCCAAC[G/T]TCATACTGAGACACA | 55230 |
rs189531668 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475193 | TTTGAGACGGAGTCT[C/T]GCTCTGTCACCCAGG | 55230 |
rs189594900 | snp | A/T | 0.0162398 | 0.0886349 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233568556 | GATATAAGATTATAT[A/T]TATATAATCTTATAT | 55230 |
rs189613401 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233528432 | AGGGTCTGACCAATG[G/T]GGAGCTGGAATGAGG | 55230 |
rs189619604 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233510719 | AACATACACTATTTC[A/T]TCTACTATGATCTCC | 55230 |
rs189624638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233548644 | AATCTGAACATAACT[A/G]TTAGACAACAGTATT | 55230 |
rs189630434 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233493254 | GCACGTACAGAAATG[A/G]CACAGTGTTATTATT | 55230 |
rs189645204 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233475991 | TGGGAGTGGGAGGCA[C/G]CTGCTAGTCAGAGTT | 55230 |
rs189657037 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233525850 | ATGAAGAGCACTTTT[C/G]TCAGAAAGCAAGTTG | 55230 |
rs189670172 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP40 | GRCh38.p7 | 2:233546338 | ACATGCTGCCTCACC[A/G]GAGTGTGAAACTGCC | 55230 |
rs189678207 | snp | C/T | 0 | 0 | intron-variant | USP40 | GRCh38.p7 | 2:233490516 | TTCATATACTGAGGG[C/T]GCACAAAAGCCAAAC | 55230 |
rs189686006 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233507551 | CCTGGAAGACATCAT[A/G]TTAAGTGAACGAAGC | 55230 |
rs189726396 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP40 | GRCh38.p7 | 2:233553886 | TACAGAAAGAAAATC[A/G]GAAGTATTCTGTTAA | 55230 |
rs189785293 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233489049 | TTTCAGGAGGAGGAT[C/G]AGCTGAATCCAACAT | 55230 |
rs189825057 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233527706 | ACAATTTTTCTTCTA[C/T]GTGCCACAATTAGTC | 55230 |
rs189834870 | snp | G/T | 0.0588605 | 0.161139 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233567762 | TAACCTTATATAAGA[G/T]TATAGTTATATAACC | 55230 |
rs189863445 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP40 | GRCh38.p7 | 2:233492527 | AACTAGAATTCTATC[A/G]CCAAGGCATTTTTAG | 55230 |
rs189904041 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233522760 | GTCTTATGGGTCTCC[G/T]GAAACAAAATATCCA | 55230 |
rs189920766 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233539566 | AGAAAATATTTCAAA[C/G]TGAATGAAAATGAAA | 55230 |
rs189923217 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486443 | GGGTTGGAATTGGGA[A/C]GAGAGACACAGGGCG | 55230 |
rs189931128 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233503479 | TTTGGGCACTTTATA[A/G]TAAGACTCTCAAAAG | 55230 |
rs189939847 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233549420 | CTAATGGCCAGTCAC[A/G]CTACACCAATCAAAT | 55230 |
rs190010625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233533026 | TAAAGGATAAATAAT[A/G]GAAATAAAAGATATA | 55230 |
rs190064231 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233545688 | AATTACACGAGATTG[A/G]TCCTGAAAACTACTC | 55230 |
rs190081888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233485171 | TTACATAATCTATTC[C/T]TCACGCTGCCCTCCT | 55230 |
rs190090797 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | USP40 | GRCh38.p7 | 2:233548335 | AATCCTATTGTGAAA[A/G]CTACAGACACGGGAT | 55230 |
rs190108990 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | USP40 | GRCh38.p7 | 2:233510673 | CCTCCCAAAGGGTTG[A/G]GATTACAGATGTGAG | 55230 |
rs190270823 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | USP40 | GRCh38.p7 | 2:233498952 | TAAAATTGAAAGGAA[G/T]CAGTGGAAGACCTGC | 55230 |
rs190285805 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233479530 | ATCGTGCCACTGCAC[C/T]CCAGCCTGGCGACAA | 55230 |
rs190291659 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233507221 | ATTTATGCACTGTCG[C/G]TGAGACTGTAAATTA | 55230 |
rs190317701 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233495212 | AAAAAATCTAGGTAC[A/G]GAATAGGTTGCCTAG | 55230 |
rs190323051 | snp | C/T | 0.000132582 | 0.00814085 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233525504 | TGGTAAATGTGAAGT[C/T]CTGCTGGTACAAGCT | 55230 |
rs190327297 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP40 | GRCh38.p7 | 2:233563312 | AAGTTGGCAACCCCA[C/T]GCGAGTCTCCAGAAT | 55230 |
rs190331600 | snp | A/G | 0.00517822 | 0.0506191 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476789 | GTGTGGCTCCTCCTC[A/G]TGGAAAGAGCTCGCA | 55230 |
rs190354582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233565202 | ACATTTCTCTGCAGA[A/G]GGAATTACCAATTTA | 55230 |
rs190369843 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP40 | GRCh38.p7 | 2:233526627 | AAAAACACAAAAAAG[C/T]TAACATTTTCTATCT | 55230 |
rs190385655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233546724 | CGATCAGAATCTAAT[A/G]AAAGGCTTCATCTTA | 55230 |
rs190388820 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233484162 | GATACTGTCTCAACA[A/C]CAACAACAAAAGAAA | 55230 |
rs190548346 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233556461 | TCCCATATTTAATTA[A/C]AAATGTTTGTCAAAT | 55230 |
rs190552980 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233554664 | TAGATCTCCTGATTA[A/G]ATGTTGTGAAGTTCA | 55230 |
rs190559390 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233533421 | ATTCAAACAGCATTC[A/C]ATGTTTATCTTCTAA | 55230 |
rs190559607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233489690 | CATATTCCTCTGCAC[C/T]GAAATCACCTTGAGA | 55230 |
rs190562474 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233518887 | TGTCCAGGATAAACA[A/C]AATGTGATACTATCC | 55230 |
rs190587002 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233481383 | CTAAAAAACTACCTA[C/T]ATTGACAAAAGAACA | 55230 |
rs190587590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233499601 | TGTCTTCCACAATGG[C/T]TGACCTAATTTACAT | 55230 |
rs190593105 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233516789 | TTGAACCCAGGAGAC[A/T]GAGGTTGTAGTGAGC | 55230 |
rs190594871 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP40 | GRCh38.p7 | 2:233499357 | TTCCTTTCTATGGCT[A/G]CACAGTATTCCATGG | 55230 |
rs190601189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233564770 | CATTAATCAAGCAGA[C/T]TAATATTCCTGTAAT | 55230 |
rs190761969 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233534842 | GTTGAGAATTAACTC[C/G/T]TTTAAGCCTCAAACA | 55230 |
rs190825805 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233500770 | TAATACATGCAAAGT[A/G]ATCCCATTTATAATT | 55230 |
rs190827874 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233538124 | TATATATAGTGTAAT[C/T]GCTAGATGAAATTAA | 55230 |
rs190849065 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233517085 | GTTGTTGTTGCTGGT[A/C]GGTAAAAAGGCAATG | 55230 |
rs190850993 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | USP40 | GRCh38.p7 | 2:233482301 | CTCGGGAGGTGGAGG[G/T]TCCAGTGAGTCAAGA | 55230 |
rs190860647 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233511065 | GGAACCATGGGCAAC[C/G]TGATTTGAGTCCAGA | 55230 |
rs190989672 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233550346 | CAGTTTTGTTACATC[A/G]AAGTATGTTAAAAAT | 55230 |
rs191022852 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | USP40 | GRCh38.p7 | 2:233555697 | CTGGAGCACAGTGGC[G/T]CAATCTCAGGTCACT | 55230 |
rs191026192 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233530206 | AATTTCACTCCCAAG[A/G]CACACACACACACAC | 55230 |
rs191032201 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP40 | GRCh38.p7 | 2:233496620 | GAAACATATCTGATT[A/G]ATAGCATTTGGGGAA | 55230 |
rs191033737 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233513096 | TGTCTTTGTAAATTA[C/T]ATATAAAGAGTCGTT | 55230 |
rs191046408 | snp | A/G | 0.00636936 | 0.0560724 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477303 | TTTGGGATTGGAGGC[A/G]CCAGGCAGCCAGTCC | 55230 |
rs191081573 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476311 | AGGACATGCGACACC[A/G]TCTTCGGGATGCTGC | 55230 |
rs191097076 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP40 | GRCh38.p7 | 2:233559145 | AGCTCATCAATATGT[A/G]CAACAAGCACCTTTA | 55230 |
rs191129053 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233529184 | ATTTCTCTACTCTTG[C/T]TAGGCTTCGATCCCT | 55230 |
rs191241222 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233547415 | TGTCAGAAATACAGA[C/T]GAACACTTTGAAAAG | 55230 |
rs191251401 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233566735 | GAAGCGAACGAACCC[G/T]CCCCAACTGGGCGCC | 55230 |
rs191270172 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233526974 | CTAGACTAGCAGATA[C/T]TTTCCTTCACTTAAG | 55230 |
rs191272594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233492026 | TACAGGCTGACACTA[C/T]CGGAAAGATAATTTT | 55230 |
rs191281377 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | USP40 | GRCh38.p7 | 2:233509429 | ATGTTAATATTGGTA[C/G]GATAAAGAATAATGA | 55230 |
rs191286236 | snp | C/T | 0.00956233 | 0.0684816 | intron-variant | USP40 | GRCh38.p7 | 2:233561148 | CACCCCAGTAAATCA[C/T]AGATGTAATACCTTT | 55230 |
rs191287865 | snp | C/T | 0.00229669 | 0.0338093 | intron-variant | USP40 | GRCh38.p7 | 2:233542252 | ACATACAAATACATA[C/T]ACACACATACTATAC | 55230 |
rs191318377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233488886 | CACTCCAGCCTGGGC[A/G]ACAGAGCCAGACCCT | 55230 |
rs191322598 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP40 | GRCh38.p7 | 2:233524240 | GTTCAAGCGATTCGC[C/T]TGCCTCAGCCTCCCA | 55230 |
rs191328650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233506051 | TCAAAGCAATTGTGA[A/G]CAAAAAGAACAGAGC | 55230 |
rs191334366 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233493963 | CTGATACAAACTAAA[A/G]GAAATAAACCCATTG | 55230 |
rs191340085 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233490911 | AAATAAAAATGAACA[A/T]AAGCCGCAAGTCACT | 55230 |
rs191357880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233516642 | GCAGTGGGCCAAGAT[C/T]GCACCACTGCACTCT | 55230 |
rs191397667 | snp | A/G | 0.000221656 | 0.0105251 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233529493 | ATGACATGGAACCCC[A/G]TATCTTGGATTAGCT | 55230 |
rs191556597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233507822 | GTATATTAAAAAATA[A/G]TTAGAAAAGCTCTTG | 55230 |
rs191567223 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233567344 | TATAACCTTATATAA[C/G]ATTATAGCTATATAA | 55230 |
rs191617253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233547022 | AGCATTTGAGAGCAA[C/T]GCTTGTACAGCTTTC | 55230 |
rs191627360 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233511945 | AAAGGATTACATGCA[C/T]TAAGATTAGGTTTGA | 55230 |
rs191636082 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233508683 | GCCTTCATTTATTAG[G/T]TGGAATATGTTTATA | 55230 |
rs191828171 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233549806 | CAACTGTTTTTGTTT[A/G]GAGGCAGTTTAGTGG | 55230 |
rs191870042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233517722 | AGCACAGTTTGCAAT[C/T]GCAAAATCATGGAAC | 55230 |
rs191887022 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | USP40 | GRCh38.p7 | 2:233500462 | TAAAACAAAAATAGT[A/T]ATTAAAACAATTTCT | 55230 |
rs191900383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233483128 | ATGATTTCCTTTGAC[A/G]AACAAAAGTTCTCAC | 55230 |
rs191950650 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233526779 | AGGCAAGACATTGAG[C/T]CTCTTTAAATCACAC | 55230 |
rs192072102 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233521596 | TTTATAATTGCAGCC[A/G]GCAGTAGAGTATCTT | 55230 |
rs192084691 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233558656 | AGTTTCTTTTTGGGG[C/T]GGTAAAAATTTTCTA | 55230 |
rs192108386 | snp | C/T | 0.000291269 | 0.0120644 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485992 | GCTGTACCAGAAAAC[C/T]GTCAAGCGCCAGATC | 55230 |
rs192114579 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233560036 | TCATTCAGGAGAAAG[C/T]TTATAAATATCCTAT | 55230 |
rs192119007 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233515188 | GATTGCTTCCAGTTT[G/T]GGGTTAGGAACATTT | 55230 |
rs192133322 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233523694 | TTTTTAGGAGAAATC[C/T]ATGATAGACTGGAGA | 55230 |
rs192135260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233497738 | TTTATGTCCTAAAGA[C/T]GCTTTGAGGTCCACT | 55230 |
rs192152945 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | USP40 | GRCh38.p7 | 2:233478548 | TTGCAGATAATGTTT[A/G]CAGCCATACCCTCTG | 55230 |
rs192153010 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | USP40 | GRCh38.p7 | 2:233540134 | AACTCAAAAAAAAAA[A/C]AAAAACAAAAAACAA | 55230 |
rs192184297 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233518514 | GGAGGTTGCAGTGAG[C/T]GGAGATCGTGTCACT | 55230 |
rs192201144 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP40 | GRCh38.p7 | 2:233537120 | AACTCCTGGGCTCAA[A/G]CAATCCTCTTGCCTA | 55230 |
rs192217994 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233500522 | GGACAAGCGAGCAAA[C/T]ACAATTTGATTTCTA | 55230 |
rs192281487 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233501183 | AAACAATCAAACAAT[G/T]GAGCAATCAACTTAA | 55230 |
rs192285296 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | USP40 | GRCh38.p7 | 2:233538510 | ATAAGTTCATATTCT[A/C]CAGTCACTAAACGGA | 55230 |
rs192369470 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233550762 | AAGTAGGTTGATTTT[A/G]TAATTAATTTGTTTT | 55230 |
rs192383732 | snp | C/T | 0.00200612 | 0.0316075 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477452 | TCGGGGCCGGGCAGG[C/T]GTCTCTGCACTGGAG | 55230 |
rs192386165 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233514699 | GAGTGGAAGAAGGGA[G/T]ACAAGTTTCATGGGA | 55230 |
rs192434170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233553219 | TAGCAATTAACTAGC[A/G]TTGGTAATGCTTTTG | 55230 |
rs192434549 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233539328 | CCTCTTTAGTGAACA[A/C]AGAACATTGAGCAGG | 55230 |
rs192459170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233503058 | TTATGAAATGCCTGA[A/G]GAGAAATTCAAAACA | 55230 |
rs192611706 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233527170 | CTTTCTTCCCCTCAA[A/G]TAAAATGTACCAGGC | 55230 |
rs192664802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233556619 | CCCAAATCTATTTTC[C/T]AAATATTAGGGTACT | 55230 |
rs192676893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233518956 | ACAAGCTATTGATAC[A/G]TACTAAATCATGGAC | 55230 |
rs192725056 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233531030 | AAAGGAACTATAATT[C/T]CATTTAAGTGATTTG | 55230 |
rs192753040 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233497277 | ACCAGGAGGTCACAC[C/T]GGACTGGAAGGGCAG | 55230 |
rs192761868 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP40 | GRCh38.p7 | 2:233556024 | GGGAGGCTAAGGCAG[A/G]AGAATGGCGTGAACC | 55230 |
rs192764845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233492320 | GTAAATCACTCTACC[A/G]TGTTCACATAATGAT | 55230 |
rs192851733 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233548000 | GGAAATTGACAATGT[A/G]GTATTTGCCCAGGAA | 55230 |
rs192896854 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233504271 | CAGAAAACGATTAAC[A/G]AAATGGCAGGAGTAA | 55230 |
rs192928667 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233483613 | GTTGACTATGGTGTG[A/C/G]GCAGAGGTAAGTACA | 55230 |
rs192963897 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233535554 | ACCCAGGGCTAAGCT[A/G]TTCCCTGGAACTAAA | 55230 |
rs192970075 | snp | C/T | 0.00478085 | 0.0486577 | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475287 | CCTGCCTCAGCCTCC[C/T]GAGTGGCTGGGACTA | 55230 |
rs192972036 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233509839 | GAGTTGAGACTCTCT[A/T]AAAAAAAAAAAAAAA | 55230 |
rs193040910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233560704 | AGGAACATGATTAGA[C/T]ATGCACTTTAAATAT | 55230 |
rs193108534 | snp | A/G | 1.71652e-05 | 0.00292955 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551412 | ATTAATCCGGAGAGG[A/G]AATGTATAACAGCTA | 55230 |
rs193130879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233524008 | ACAACCTGGTATAAC[A/G]GAGGCGCTCAAGAAA | 55230 |
rs193134844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233487743 | TTGACTATGACATGG[A/G]CACAATTACTATTCT | 55230 |
rs193176157 | snp | C/T | 4.40189e-05 | 0.00469122 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233491247 | AAACTTGCGCAGGCT[C/T]GTTCCCAGAAGCACC | 55230 |
rs193281554 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233541173 | AAGTATAAACAAGTT[A/C]TAAAAGGGGGTGAGA | 55230 |
rs193282786 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233504892 | ACAGTCCATCAACAA[A/C]TGCAGGATACACATT | 55230 |
rs199540416 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556912 | GTTAACAATGGTTCC[A/G]TGGTACAGACGATAG | 55230 |
rs199547362 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233492086 | CACCTGCTACATAAT[G/T]ATTTGGTCAAAGACC | 55230 |
rs199550497 | snp | A/G/T | 0.00874735 | 0.0655527 | intron-variant | USP40 | GRCh38.p7 | 2:233553064 | GGGTTGATGCCATAG[A/G/T]AGCTGAGAAGGAAGG | 55230 |
rs199592795 | snp | C/T | 1.72389e-05 | 0.00293584 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477387 | AGAGCCGTGCAGCGG[C/T]GCGGTTATCTGAAGC | 55230 |
rs199622950 | snp | C/T | 0.000707307 | 0.0187924 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233510071 | ACAGATATTGTTTCT[C/T]CTACTACGATTTCCA | 55230 |
rs199634773 | snp | C/T | 0.000811238 | 0.0201236 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523254 | TTCCTCATGTCTTCC[C/T]TGGGGATGGCCGTCC | 55230 |
rs199657112 | snp | C/T | 0.00299544 | 0.0385843 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523453 | TTAAAAGTAGAGGTT[C/T]GCAGTCAATACCAGT | 55230 |
rs199673480 | in-del | -/TTATT | 0.00557542 | 0.0525036 | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475157 | GGCCACAAACGTTCC[-/TTATT]TTATTTATGTATTTT | 55230 |
rs199707769 | in-del | -/C | 0.0490535 | 0.14873 | intron-variant | USP40 | GRCh38.p7 | 2:233512800 | AAAACAAACCAAAAA[-/C]CCCCCAACAACCAAA | 55230 |
rs199782012 | in-del | -/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233529814 | TTTCTTTTTCTTTTT[-/C]TTTTTTTTTTTGAGA | 55230 |
rs199833993 | snp | A/C | 7.53338e-05 | 0.00613688 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485758 | TCTGAGACAGCCCCA[A/C]AACTTTACCCAGCTA | 55230 |
rs199834849 | snp | A/T | 0.000415327 | 0.0144046 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233496813 | CCAGAACATATCAGA[A/T]GTTCTTTCAGTGTTG | 55230 |
rs199839652 | snp | C/T | 6.70893e-05 | 0.00579139 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527450 | AAAGTTTTTCTTTTA[C/T]CAAAGGTCAAATCCC | 55230 |
rs199989761 | in-del | -/TAGCTGGGC | | | intron-variant | USP40 | GRCh38.p7 | 2:233506763 | AAAAAAAAAAAAAAA[-/TAGCTGGGC]ATAGTAGCATATACC | 55230 |
rs199991772 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233555345 | ATTTGGCAAATTTAA[G/T]TTATATTTATAGTTC | 55230 |
rs200057020 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233484937 | AGGGGCGGTTAGGGG[C/T]ATCCTTACTTTGGGT | 55230 |
rs200068889 | snp | C/G | 0.000417554 | 0.0144431 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233524544 | GCAATTTCAGTTTCA[C/G]ACAGTGTCAGTTCAT | 55230 |
rs200139615 | in-del | -/A | 0.0532157 | 0.154195 | intron-variant | USP40 | GRCh38.p7 | 2:233561105 | CTTAATTCCTTCTTT[-/A]AAAAAAAATTTTCTG | 55230 |
rs200143759 | in-del | -/CC | | | intron-variant | USP40 | GRCh38.p7 | 2:233507893 | TGAGTATGCTAAATA[-/CC]CTGATTTAATCATTA | 55230 |
rs200144577 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233556298 | TTCCAATTTCTAATT[C/T]CCAATTAGATTAAAT | 55230 |
rs200152165 | snp | C/T | 0.00018285 | 0.0095599 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233496774 | AGAGGAGGAAGTTGT[C/T]CTTCAATTAAAAGCA | 55230 |
rs200178733 | in-del | -/G | | | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475148 | GGAAAAAGGGCCACA[-/G]AACGTTCCTTATTTT | 55230 |
rs200328029 | in-del | -/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233527981 | CACATTCTCCCATGA[-/T]TTTTTTTTTTTTTTT | 55230 |
rs200363827 | snp | A/C/T | 0.00121565 | 0.0246244 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233554523 | TTAGATCTAAGAAGT[A/C/T]TTCCTGAAATAGACA | 55230 |
rs200394290 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233488722 | AGTTCGCGACCAGAC[C/T]GGGCAACATAGGGAG | 55230 |
rs200397517 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233553061 | GCAGGGTTGATGCCA[A/T]AGAAGCTGAGAAGGA | 55230 |
rs200423585 | snp | A/G | 0.000423888 | 0.0145521 | intron-variant | USP40 | GRCh38.p7 | 2:233549097 | AACGAATTTCTATAC[A/G]TACTTGAAACTGCCA | 55230 |
rs200438807 | in-del | -/G | 0.0486741 | 0.148216 | intron-variant | USP40 | GRCh38.p7 | 2:233518208 | ATGTGCTCAAAATAT[-/G]GTTTTTTTTTTTAAA | 55230 |
rs200514706 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233497219 | TAGTAAATATGGCTT[G/T]TTTTGGTAAAGCGCT | 55230 |
rs200624947 | snp | C/G/T | 1.66073e-05 | 0.00288156 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233554490 | CTTCCAAACCGGATA[C/G/T]ATTTTTGACTGCTAC | 55230 |
rs200695152 | in-del | -/G | 0.31503 | 0.241394 | intron-variant | USP40 | GRCh38.p7 | 2:233506754 | CAAAAAAAAAAAAAA[-/G]AAAAAAAATAGCTGG | 55230 |
rs200698587 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233553839 | AGTTGCTTCAGTCCT[G/T]ACTTTCTTTTGTCTT | 55230 |
rs200707107 | snp | C/T | 3.63636e-05 | 0.00426386 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233521099 | AGTGACCCATTTCTC[C/T]TCCTTGGTCAACAAG | 55230 |
rs200754546 | in-del | -/GC | 0.00795532 | 0.062565 | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475435 | CCCAAAGTGCTGGGA[-/GC]TTACAGGCGTGAGCC | 55230 |
rs200793850 | snp | A/G | 0.000134878 | 0.00821101 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477445 | CCGGGGCTCGGGGCC[A/G]GGCAGGCGTCTCTGC | 55230 |
rs200831312 | snp | C/T | 0.000637395 | 0.0178407 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485967 | GTGTCCTCAGCAGCA[C/T]GTCCTGGGGGCTGTA | 55230 |
rs200958963 | snp | C/T | 1.81414e-05 | 0.00301171 | intron-variant | USP40 | GRCh38.p7 | 2:233499871 | TGTCATCATGGTAAG[C/T]AACTTACCTTGTAGG | 55230 |
rs200980543 | in-del | -/T | 0.0490535 | 0.14873 | intron-variant | USP40 | GRCh38.p7 | 2:233540435 | GGATGAACTCTGACA[-/T]TTTTTAGGAGTCACT | 55230 |
rs200982571 | in-del | -/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233482598 | TTTTTTTTTTTGTTT[-/G]TTTTTTTTTTGACAC | 55230 |
rs200985105 | snp | C/T | 0.000109529 | 0.00739949 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533724 | CTATTCTTCAAGAGA[C/T]GAACTGTACTTTCAT | 55230 |
rs201011920 | snp | C/T | 6.27609e-05 | 0.00560147 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233489453 | CTGGGGACGGGACAC[C/T]GAACTCCAGGAAAGG | 55230 |
rs201030790 | snp | A/G | 0.000170567 | 0.00923333 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556864 | ATTTACCTGCCTCTC[A/G]CTAACGTTCTTACAT | 55230 |
rs201073202 | snp | A/T | 0.000167986 | 0.00916323 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556904 | ACAATCTGGTTAACA[A/T]TGGTTCCATGGTACA | 55230 |
rs201097038 | snp | C/T | 0.0039921 | 0.0444985 | intron-variant | USP40 | GRCh38.p7 | 2:233527592 | CCCTTTAAAGAGGCA[C/T]AAAAATACATAAATA | 55230 |
rs201104478 | snp | A/G | 0.000268281 | 0.0115788 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233493466 | CTGCCCCAAGACGAA[A/G]TACAGTTGGTCTGGT | 55230 |
rs201108397 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233533792 | GAACTACACAGAAAC[A/C]AAAAAAAAAATGCTA | 55230 |
rs201123578 | snp | C/T | 0.000282052 | 0.0118721 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233554484 | GAGCATCTTCCAAAC[C/T]GGATACATTTTTGAC | 55230 |
rs201148037 | in-del | -/CAT | 0.0213246 | 0.101033 | intron-variant | USP40 | GRCh38.p7 | 2:233524600 | ACCATTCATCATGAC[-/CAT]CAGAAACAACTGAGC | 55230 |
rs201158912 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562560 | CCCCCAACCCACAAC[A/T]GTCCCCAGAGTGTGA | 55230 |
rs201166361 | snp | A/G/T | 0.000182455 | 0.00954977 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233525479 | CATATTTATCTTACC[A/G/T]CCAAGTGACTGGTAA | 55230 |
rs201200560 | in-del | -/AGAG | 0.00318978 | 0.0398085 | intron-variant | USP40 | GRCh38.p7 | 2:233501221 | TTAGGAAGGGGAAAT[-/AGAG]AGCATAAAAGCCTTA | 55230 |
rs201293941 | in-del | -/C | | | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475151 | AAAAAGGGCCACAAA[-/C]GTTCCTTATTTTATT | 55230 |
rs201340272 | in-del | -/GT | | | intron-variant | USP40 | GRCh38.p7 | 2:233479660 | TGTGTGTGTGTGTGT[-/GT]CTGACCTTTAAACAG | 55230 |
rs201347288 | snp | C/G | 0.00037657 | 0.0137165 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527532 | GATACTGAGGGCCCA[C/G]GTGAAGATGCAATTC | 55230 |
rs201372687 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233539142 | GTCAAAACTTTTTTT[A/T]AAAAAAATGAGACAA | 55230 |
rs201378346 | in-del | -/AAT | 0.0204309 | 0.098985 | intron-variant | USP40 | GRCh38.p7 | 2:233496715 | CTGTAATCAGATAAC[-/AAT]AATTATTACTTAAGA | 55230 |
rs201387069 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233555126 | TGAACCTGGGAGGCG[A/G]AGGTCGCAGTGAGCC | 55230 |
rs201398922 | snp | A/G | 1.66746e-05 | 0.00288739 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233524529 | ATGTCTTCCCCATCA[A/G]CAATTTCAGTTTCAC | 55230 |
rs201403979 | in-del | -/T | 0.0659589 | 0.169201 | intron-variant | USP40 | GRCh38.p7 | 2:233509837 | AGAGTTGAGACTCTC[-/T]TAAAAAAAAAAAAAA | 55230 |
rs201413521 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233553840 | GTTGCTTCAGTCCTG[A/T]CTTTCTTTTGTCTTA | 55230 |
rs201446243 | snp | C/G | 0.000280134 | 0.0118317 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233489436 | CCAGGCTCTGAGGTG[C/G]GCTGGGGACGGGACA | 55230 |
rs201451781 | snp | C/T | 0.00299553 | 0.0385849 | intron-variant | USP40 | GRCh38.p7 | 2:233561072 | TAATTAATAAAATTA[C/T]TGCTTTGTGAACAAG | 55230 |
rs201458545 | in-del | -/CAG | 0.2776 | 0.248472 | intron-variant | USP40 | GRCh38.p7 | 2:233518243 | AAACCAAACCAGTAA[-/CAG]CAGATTCTAAAAAAA | 55230 |
rs201460247 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233554443 | GTCACAATCAAAAAC[C/T]TCCTCTTCTACATAC | 55230 |
rs201480644 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233539264 | AACACAATCAATTTG[A/G]CCTAGTTGTCACTTG | 55230 |
rs201507602 | snp | A/G | 5.4781e-05 | 0.00523331 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485791 | TATCGGAAGCCACTC[A/G]AACTTTTCGGGAAAG | 55230 |
rs201542458 | snp | C/G/T | 0.000493205 | 0.015696 | intron-variant | USP40 | GRCh38.p7 | 2:233498504 | TACGAAAATATGACA[C/G/T]AAATGTAATCATACG | 55230 |
rs201639376 | snp | A/G | 0.000722028 | 0.0189866 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485822 | TATTTGGCAATTTCA[A/G]TCTTCTCCACGGGAA | 55230 |
rs201644858 | in-del | -/T | 0.0588605 | 0.161139 | intron-variant | USP40 | GRCh38.p7 | 2:233558880 | TTAGGGAATGTATTA[-/T]TACCCCATTTTGCTT | 55230 |
rs201645171 | in-del | -/TG | | | intron-variant | USP40 | GRCh38.p7 | 2:233494856 | AACCAAAAAAAAAAC[-/TG]TGCAATTTCAGTTCT | 55230 |
rs201649817 | snp | C/T | 0.000134871 | 0.0082108 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477438 | GAAGTTTCCGGGGCT[C/T]GGGGCCGGGCAGGCG | 55230 |
rs201656029 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233539211 | TAATTAATAGAAAAG[C/G]CAAAAAAAAAAATAA | 55230 |
rs201698413 | in-del | -/A | 0.0322114 | 0.122752 | intron-variant | USP40 | GRCh38.p7 | 2:233516329 | CTTGTCAATTTCTTT[-/A]AAAAATGTTAAGATT | 55230 |
rs201747711 | snp | A/G | 0.000227071 | 0.0106529 | intron-variant | USP40 | GRCh38.p7 | 2:233559942 | GAATGAGAAACAAAC[A/G]CATTTCTAAATGAAT | 55230 |
rs201754347 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233553063 | AGGGTTGATGCCATA[G/T]AAGCTGAGAAGGAAG | 55230 |
rs201791599 | snp | A/G | 0.000897414 | 0.0211637 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485977 | CAGCACGTCCTGGGG[A/G]CTGTACCAGAAAACC | 55230 |
rs201936203 | snp | C/G | 0.000240248 | 0.0109575 | intron-variant | USP40 | GRCh38.p7 | 2:233554365 | CCCTGGGAAAAAGCA[C/G]TTATCTGTCTTTACC | 55230 |
rs201945738 | in-del | -/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233517387 | ATGCATGGTTTTTTG[-/T]TTTTTTTTTTTTTTT | 55230 |
rs201966113 | snp | A/C/G/T | 0.000126906 | 0.00796496 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485850 | GAAGACGATAGAAAT[A/C/G/T]GGCAACTCTCTGCCT | 55230 |
rs201970236 | snp | C/T | 0.00120542 | 0.0245205 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233491237 | TAGAGGAGAGAAACT[C/T]GCGCAGGCTCGTTCC | 55230 |
rs201971737 | snp | C/T | 3.52765e-05 | 0.00419964 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233521096 | ACTAGTGACCCATTT[C/T]TCTTCCTTGGTCAAC | 55230 |
rs201975946 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233560354 | TCACTTTCTCCTGGC[G/T]CCAAGTGAGTTCCTG | 55230 |
rs202019246 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233515765 | AAAACCTTTCCTTAT[G/T]ATAAAGTAACAAAGA | 55230 |
rs202030309 | snp | A/G | 0.00299544 | 0.0385843 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233525516 | AGTCCTGCTGGTACA[A/G]GCTTTGCAACACTAA | 55230 |
rs202051483 | snp | C/T | 0.000264945 | 0.0115066 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523347 | GCTGTGAGGACAGTG[C/T]CCACTTCTGCATTAG | 55230 |
rs202051951 | snp | C/G | 0.00137218 | 0.0261573 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233554511 | TGACTGCTACTGTTA[C/G]ATCTAAGAAGTCTTC | 55230 |
rs202066075 | snp | A/C | 1.65787e-05 | 0.00287907 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533590 | GCTGGACTTTAGAAT[A/C]ATTTATATCAAACCA | 55230 |
rs202182823 | snp | A/G | 3.20868e-05 | 0.00400529 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233549146 | ATCTTTAATATATAC[A/G]TGGTAATGGCCTCCG | 55230 |
rs202226925 | in-del | -/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233517379 | CTTGCACATGCATGG[-/T]TTTTTTGTTTTTTTT | 55230 |
rs202235068 | snp | C/G | 9.94118e-05 | 0.00704954 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233540712 | TGTTCCAAGATATTC[C/G]TATCTTTTTCAAAAG | 55230 |
rs367551732 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233481551 | AGAAGCTTCCACTGC[A/G]AGTGGCCAAACAGGG | 55230 |
rs367609064 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233485464 | GAAGATTCAATAAAA[C/T]GTCTCTATAAAATCA | 55230 |
rs367630032 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233494608 | TGGTGGCTCACAGCT[A/G]TAATCCCAGTACTTT | 55230 |
rs367636109 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233515852 | GTATGATCCATTTAA[C/T]TTTTGCATCAGGCGA | 55230 |
rs367639854 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233533939 | TCTAGGTATCATAAA[A/G]CATTTAATAAAACCA | 55230 |
rs367655651 | snp | A/G | 0.000169986 | 0.00921759 | intron-variant | USP40 | GRCh38.p7 | 2:233496729 | ACAATTATTACTTAA[A/G]AGTTGTCTATTCAGA | 55230 |
rs367662150 | snp | A/G | 0.000135293 | 0.00822363 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477410 | TCTGAAGCTCCCCAC[A/G]TGGATGGAGAGAGAA | 55230 |
rs367688735 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP40 | GRCh38.p7 | 2:233488742 | AACATAGGGAGACCT[C/T]GTCAAAACAAAAAAT | 55230 |
rs367703631 | in-del | -/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233483963 | CACATTTCCTCACGT[-/T]GTGTGATTCTGTTTC | 55230 |
rs367735273 | snp | C/T | 0.000327946 | 0.012801 | intron-variant | USP40 | GRCh38.p7 | 2:233523119 | TTCTGCTGGGTGGTA[C/T]TGTAATTAAAATGAC | 55230 |
rs367756872 | snp | A/G | 0.000106197 | 0.00728608 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485896 | CCCACCCTGGGCCGC[A/G]TTCCACACCAGGTCC | 55230 |
rs367817261 | in-del | -/AGGA | | | intron-variant | USP40 | GRCh38.p7 | 2:233506820 | GGAGGCTGAGATGGA[-/AGGA]TCACTTGAGCCCTGG | 55230 |
rs367819232 | snp | A/G | 0.000967618 | 0.0219744 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233481280 | ACTGAAATCATCATC[A/G]TCGTCAATCAGGAGA | 55230 |
rs367827197 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233558001 | AGTGAGACCTCATCT[A/C]AAAAAAAAAAAAAAA | 55230 |
rs367828654 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233518498 | CTTGAGCCTGGGAGA[C/T]GGAGGTTGCAGTGAG | 55230 |
rs367849310 | in-del | -/A | 0.234401 | 0.249513 | intron-variant | USP40 | GRCh38.p7 | 2:233494825 | AGTCAGATCCTTTCT[-/A]AAAAAAAAAAAAAAA | 55230 |
rs367857072 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233557585 | AATTTATAACCAAAC[C/T]AAGGGGCACACCAAG | 55230 |
rs367860946 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476724 | CCTGCGGGCTGACGT[A/G]CAGCGGCTGCCCTTG | 55230 |
rs367906855 | snp | A/T | 0.000464551 | 0.0152335 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485512 | CTCAAAGTGGTAAAT[A/T]TGCTGTTAAACAACT | 55230 |
rs367924687 | snp | C/G | 0.000157988 | 0.00888644 | intron-variant | USP40 | GRCh38.p7 | 2:233489330 | AGTGCGTCAGCAGCA[C/G]AGAGGGACAGTGTTG | 55230 |
rs367936964 | snp | C/T | 1.68613e-05 | 0.00290351 | intron-variant | USP40 | GRCh38.p7 | 2:233524575 | CCCCTAGAAAGAGAT[C/T]ACCAGTGAGACCATT | 55230 |
rs367953988 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233503641 | AGGAAAGAAAAAAAC[A/C]CTGTCAGCCAAGAAT | 55230 |
rs367965995 | snp | C/T | 1.66217e-05 | 0.0028828 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556894 | TTCTTTACAAACAAT[C/T]TGGTTAACAATGGTT | 55230 |
rs368016092 | snp | C/T | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486550 | CAGGAGGAACAGGGA[C/T]GTGCAGAGGTCAGCA | 55230 |
rs368028760 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233507864 | CACCAAGAAATGCTA[A/G]GTGCATGAGGTAATG | 55230 |
rs368040314 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233542985 | CTGGTCTTCATCCCG[C/T]ATGGTCTCATTCACT | 55230 |
rs368056472 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233561060 | GAGCATATTTGATAA[C/T]TAATAAAATTATTGC | 55230 |
rs368061598 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233501622 | CAGATCCTAGATGCA[C/T]TTTGATGGTAGAACC | 55230 |
rs368082358 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233516914 | GTGAATGTTGTATAT[C/T]GCTTTATTTATTCAG | 55230 |
rs368090935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233532617 | CTTTGCTTTGCTGGG[C/T]GTTTTGTCTAATTCT | 55230 |
rs368100283 | snp | C/T | 1.68692e-05 | 0.00290419 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233493476 | ACGAAGTACAGTTGG[C/T]CTGGTCCTGATGACT | 55230 |
rs368111016 | snp | A/G | 0.00017313 | 0.00930243 | intron-variant | USP40 | GRCh38.p7 | 2:233529393 | AGATCTTTATTCTCC[A/G]GAATACTAGTCAAAC | 55230 |
rs368113464 | snp | A/G | 9.17452e-05 | 0.00677231 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551479 | TTAAATCTTAGTAAT[A/G]AAACAGTAAGAAAAG | 55230 |
rs368115807 | snp | A/C | 0.000134382 | 0.00819589 | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233561209 | CCAAGCTCTTCTGGG[A/C]CAAGAGAAAATAAAG | 55230 |
rs368135434 | snp | C/T | 4.99388e-05 | 0.00499669 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523201 | AATCCTGAATTAAAA[C/T]TGAGCTTCCATTTCT | 55230 |
rs368208559 | snp | A/G | 3.82526e-05 | 0.0043732 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477368 | CGGAGAGTTCATCGG[A/G]AGTAGAGCCGTGCAG | 55230 |
rs368260388 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233510015 | AACATACAAACACAC[A/C]CAGCCTCTGAAAACA | 55230 |
rs368320704 | snp | C/G | 0.000116089 | 0.00761781 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556910 | TGGTTAACAATGGTT[C/G]CATGGTACAGACGAT | 55230 |
rs368325958 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233505685 | TTTCAGTAATAAAGT[C/T]TTTCATCAAAGAAAA | 55230 |
rs368356819 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233540147 | AAAAAAAACAAAAAA[A/C]AAACCAAAAAAAAAC | 55230 |
rs368363244 | snp | C/T | 0.000157987 | 0.00888644 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233489374 | ACCTACCTGAGTGGC[C/T]GCCGGTCAGTTCGTA | 55230 |
rs368386083 | snp | C/T | 0.000121073 | 0.00777957 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233481224 | CTTCTCCCCAGGGCC[C/T]GTTGTTTCTGCTTTT | 55230 |
rs368450895 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233520618 | AAAAACAGAAGTCCA[C/T]AACACAAAACCAAAA | 55230 |
rs368454102 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233527649 | TTTATCTCAAACCAA[A/C]GATATCTGGCTTACA | 55230 |
rs368466746 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233497007 | TACAGCATTATTTGT[G/T]AAATTGTGGGGCATA | 55230 |
rs368468531 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233500350 | ATGACTGTCTGAATT[C/T]CCCCGTTTTCCCTAA | 55230 |
rs368500325 | snp | C/G | 0.000169986 | 0.00921759 | intron-variant | USP40 | GRCh38.p7 | 2:233499955 | GTTAGTTTTCTGTTT[C/G]TGAGTTACAGTTCTA | 55230 |
rs368516524 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233546702 | CTTACCAGACATGGA[C/T]AAGCTTCGATCAGAA | 55230 |
rs368536892 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476083 | CACGTGTGCAGAAGC[C/G]ACGTGGCTTCTGTCT | 55230 |
rs368566732 | snp | C/T | 1.87324e-05 | 0.00306037 | stop-gained, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233493525 | ACCCTGAAGCTGGTA[C/T]CACCAGATGGGCACC | 55230 |
rs368576182 | in-del | -/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233536883 | TGTATTAGGTTTTTT[-/T]GTTTCCTTTTTTTTC | 55230 |
rs368576563 | snp | A/G | 0.000340657 | 0.0130466 | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233561250 | ACCAAAAAAGAGCCC[A/G]CATCGCCAAGTCAAT | 55230 |
rs368597027 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233494918 | CAAGCAAAATGGCAT[-/A]TATATATATATATAT | 55230 |
rs368598378 | snp | C/T | 4.92356e-05 | 0.00496139 | intron-variant | USP40 | GRCh38.p7 | 2:233481318 | TTTCAAAAGAAGTAA[C/T]GAGCAGTGTTTTCTG | 55230 |
rs368611872 | snp | A/C | 0.000167986 | 0.00916323 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233540692 | ATGCTGTTTTCTGTA[A/C]TTCTTGTTCCAAGAT | 55230 |
rs368616040 | snp | A/G | 3.95171e-05 | 0.00444488 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233510079 | TGTTTCTTCTACTAC[A/G]ATTTCCATTTCTGTC | 55230 |
rs368634805 | in-del | -/AT | 0.00676609 | 0.0577691 | intron-variant | USP40 | GRCh38.p7 | 2:233552698 | AAAAACTGGATGGAA[-/AT]ATACATGTGAAACAG | 55230 |
rs368645546 | in-del | -/AGC | | | intron-variant | USP40 | GRCh38.p7 | 2:233489855 | AAGGGACACAACAGC[-/AGC]CTTCTTCCGTGCCCG | 55230 |
rs368675542 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233538171 | ACAAAAGAGCTAAAA[A/T]TGGGACACTAAAAAT | 55230 |
rs368680590 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233530091 | AGGCATAAGCCACCA[C/T]GCCTGGCCTCAGATT | 55230 |
rs368690626 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233501997 | AGCCCAGTGACAAAA[C/G]TGTTTCAAAGAATAG | 55230 |
rs368747102 | snp | C/T | 0.000185466 | 0.009628 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233529457 | CAGTTCAATGTTAGC[C/T]GCATCCATTTCATTC | 55230 |
rs368759192 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233479533 | GTGCCACTGCACTCC[A/C]GCCTGGCGACAAGGT | 55230 |
rs368773962 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233535927 | AAGTATTTGAGATGA[C/T]GGATATGTTCATTAG | 55230 |
rs368853281 | snp | A/C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233510220 | TTTCAAAAATGTAAA[A/C/G]CCAAGGGCCCATGAA | 55230 |
rs368921262 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233536885 | TATTAGGTTTTTTTG[C/T]TTCCTTTTTTTTCTT | 55230 |
rs368933458 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233563097 | CATGGCTTCCCACTG[C/T]CTATGGCATCAGGTC | 55230 |
rs368991380 | snp | A/G | 0.000165986 | 0.00910854 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233554453 | AAAACTTCCTCTTCT[A/G]CATACATGTTCCAGA | 55230 |
rs369019472 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233521339 | CATAATTTGTTGCCA[C/T]ATTTTTCACAGAGAA | 55230 |
rs369023446 | snp | A/G | 0.000509338 | 0.0159502 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233491183 | TGAGACTTCAGCTCC[A/G]CCAGCGTGGCATCTT | 55230 |
rs369037712 | snp | A/G/T | 0.000171991 | 0.00927189 | intron-variant | USP40 | GRCh38.p7 | 2:233527386 | CGATGTCTGAATTAA[A/G/T]AGGAAGTAAGGCGAT | 55230 |
rs369044580 | snp | C/T | 0.000155842 | 0.00882591 | intron-variant | USP40 | GRCh38.p7 | 2:233559802 | TCCTTAAAGAGCTGA[C/T]CCTCGTACCTCATTA | 55230 |
rs369071345 | in-del | -/TTTTTT | 0 | 0 | intron-variant | USP40 | GRCh38.p7 | 2:233529825 | TTTCTTTTTTTTTTT[-/TTTTTT]GAGACGGAGTCTCAC | 55230 |
rs369078521 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233550669 | TAAGAATGATTTGTG[A/G/T]TAAGAAATAATTACT | 55230 |
rs369090558 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233547737 | TAAAACTTTTTAATA[A/C]GACATTAAAGGGACT | 55230 |
rs369102303 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233489560 | TTTAGAAAAAAAAAA[C/T]GAAGCACTACACAGT | 55230 |
rs369160957 | snp | C/T | 9.15457e-05 | 0.00676495 | intron-variant | USP40 | GRCh38.p7 | 2:233519712 | CTAAGTTGTAAAAAA[C/T]GGGAGGAGATGAAAA | 55230 |
rs369208011 | in-del | -/GGC | | | intron-variant | USP40 | GRCh38.p7 | 2:233534123 | AAGCAATCTAAACAA[-/GGC]ACAAAACAAAGGCAA | 55230 |
rs369214790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233503349 | TGACAAAAGACACAG[C/T]GTATCTATTTAATTA | 55230 |
rs369243255 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486028 | AAACAAACAAAACCA[C/T]GTGGTAACTTGAGGC | 55230 |
rs369248997 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233520450 | GAAAAAAAACCCATA[-/A]TGAATTGAGACTACA | 55230 |
rs369260453 | snp | C/T | 1.71764e-05 | 0.00293051 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523462 | GAGGTTCGCAGTCAA[C/T]ACCAGTTTGAATGTG | 55230 |
rs369334781 | snp | A/G | 3.31713e-05 | 0.00407242 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533509 | GCAACTGGGATTTCC[A/G]ATAAAACAACATGTA | 55230 |
rs369350230 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233534743 | ACTTGAAAGCTTTGA[A/G]TAATGAACTTTCTTT | 55230 |
rs369355138 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233494955 | ATATATATATATATA[A/T]TTATATATATATATA | 55230 |
rs369384932 | snp | A/C | 0.000161987 | 0.00899817 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477443 | TTCCGGGGCTCGGGG[A/C]CGGGCAGGCGTCTCT | 55230 |
rs369454731 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233494945 | ATATATATATATATA[A/T]ATATATATATTTATA | 55230 |
rs369483752 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233512048 | AGTCTAGTTTCCTAC[G/T]TAATAAAAATGACTT | 55230 |
rs369492031 | snp | A/C | 0.00119928 | 0.0244582 | intron-variant | USP40 | GRCh38.p7 | 2:233531634 | AGAAAAATACAAAGC[A/C]TTTTTCATTAACAGC | 55230 |
rs369500461 | snp | C/T | 5.30983e-05 | 0.00515231 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233559896 | AGCTGAGCAAACAAG[C/T]GCTGTAACTGTAAAG | 55230 |
rs369507657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233517041 | TATGCTATTATAAAT[A/G]TTTTCTTAATTTTGA | 55230 |
rs369513307 | snp | A/T | 5.05335e-05 | 0.00502635 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485576 | GTAATACGGTGCCCC[A/T]TGCAAATAATCTTGT | 55230 |
rs369566596 | snp | C/T | 0.000182844 | 0.00955974 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233496775 | GAGGAGGAAGTTGTC[C/T]TTCAATTAAAAGCAA | 55230 |
rs369596273 | snp | G/T | 0.000167986 | 0.00916323 | intron-variant | USP40 | GRCh38.p7 | 2:233521158 | TAATACCTTTCCTTA[G/T]GCATCACTTCCAAAA | 55230 |
rs369671305 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475078 | TTATTTCTAAAGCAG[C/T]ACTGCTGCAGTATTT | 55230 |
rs369689141 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233509169 | AACCTGTATCAGGGG[A/T]CAGAGCTGGAAAAAA | 55230 |
rs369693191 | snp | C/T | 1.65614e-05 | 0.00287757 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523312 | TGTTGATGAAGATGA[C/T]ACCTGCTGGGATTGC | 55230 |
rs369705346 | snp | C/G | 3.37598e-05 | 0.00410838 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477455 | GGGCCGGGCAGGCGT[C/G]TCTGCACTGGAGAGG | 55230 |
rs369709327 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233502869 | CCTAGAATCCATCTA[C/T]AGGAAAAAGCTCCTC | 55230 |
rs369726897 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233527863 | CTAATTCTGAGATTA[G/T]ATTATAGTTATGAAC | 55230 |
rs369733556 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | USP40 | GRCh38.p7 | 2:233555530 | AATGGCCTTACATAT[A/G]TTGTTTTGAAAATAC | 55230 |
rs369747973 | snp | C/G | 0.000167986 | 0.00916323 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233511731 | GAACTTGGTGCTTTT[C/G]CAAGACACAGTCCCA | 55230 |
rs369754257 | snp | C/T | 0.000116507 | 0.00763151 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485945 | CTCTCACCAGGGATG[C/T]GCACCTGTGTCCTCA | 55230 |
rs369765906 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233544018 | ATCAGGTGACAGCAC[A/G]GACTCCATAAGTTGA | 55230 |
rs369795373 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233558372 | GATTAAAAAAAAAAA[-/A]CAAAAAACATGTGGC | 55230 |
rs369870752 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233483184 | TCTTTCATGGTTTGC[A/G]CTTTCTGTTTAAGAA | 55230 |
rs369879863 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233492152 | GTATTTTCACTGTAC[A/C]TTTTTCTGTTTAGAT | 55230 |
rs369886009 | snp | A/T | 0.000169986 | 0.00921758 | intron-variant | USP40 | GRCh38.p7 | 2:233542378 | CCTAGGAAGGAAAAC[A/T]GTATGAGTTTCTATC | 55230 |
rs369906283 | in-del | -/AGAG | | | intron-variant | USP40 | GRCh38.p7 | 2:233479224 | CTAAGGCTTTGACAG[-/AGAG]GATGCTTGGAGAAGT | 55230 |
rs369926451 | snp | A/G | 4.97006e-05 | 0.00498476 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485968 | TGTCCTCAGCAGCAC[A/G]TCCTGGGGGCTGTAC | 55230 |
rs369947434 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233506409 | CTACTAAAGGAAAAC[A/G]TAGGGGGAACACTAT | 55230 |
rs369955085 | snp | G/T | 0.000502588 | 0.0158443 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527491 | TGTTTGAGAGACTAC[G/T]GGGTGCAGAGCCCCA | 55230 |
rs369966937 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233558759 | AGAGTGAATTCTGTG[G/T]CATGTAAATTACATC | 55230 |
rs369969860 | snp | C/T | 0.000116041 | 0.00761624 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533592 | TGGACTTTAGAATCA[C/T]TTATATCAAACCAGT | 55230 |
rs370006783 | snp | C/G | 3.31477e-05 | 0.00407096 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233525497 | AAGTGACTGGTAAAT[C/G]TGAAGTCCTGCTGGT | 55230 |
rs370076373 | snp | A/G | 1.66297e-05 | 0.0028835 | stop-gained, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533668 | GCATCTTGAAAATTT[A/G]CTGGTCATTCCTTTG | 55230 |
rs370077496 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233494935 | ATATATATATATATA[C/T]ATATATATATATATA | 55230 |
rs370078049 | snp | A/G | 0.000299906 | 0.0122418 | intron-variant | USP40 | GRCh38.p7 | 2:233498520 | AAATGTAATCATACG[A/G]AAGTACAATGTATAG | 55230 |
rs370139124 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233483938 | TTTTTAATGTTGCCT[C/G]AAGTATCTGTCACAT | 55230 |
rs370149552 | snp | A/C | 6.27714e-05 | 0.00560194 | intron-variant | USP40 | GRCh38.p7 | 2:233556837 | TAACTTATTACTAAA[A/C]TACTCTGGCATATTT | 55230 |
rs370156608 | in-del | -/AT | | | intron-variant | USP40 | GRCh38.p7 | 2:233494992 | ATACACACACATAAA[-/AT]AAATAAATAAATAAA | 55230 |
rs370186522 | snp | A/G | 9.28548e-05 | 0.00681313 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233489446 | AGGTGGGCTGGGGAC[A/G]GGACACCGAACTCCA | 55230 |
rs370269251 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP40 | GRCh38.p7 | 2:233548427 | ATCTAAATCAATGCT[C/T]ATTTTATTTTTCAGA | 55230 |
rs370277969 | snp | C/T | 0.00186891 | 0.0305117 | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233561168 | GTAATACCTTTGCAT[C/T]GGGTTTATCCTTATC | 55230 |
rs370313577 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233484642 | GTGTGCTACCACACC[C/T]GGCTAATTTTTGTAT | 55230 |
rs370325565 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233507167 | TATTAAAAAAACAAG[A/G]GAAAACATGTATTTA | 55230 |
rs370337489 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233541888 | CAATTTGGTTTAAAA[C/T]GACAATAATAGCCAA | 55230 |
rs370344819 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233488149 | AAGCAGTGAAAAAAA[-/A]TGCTACACTATGAAG | 55230 |
rs370370179 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233509895 | ATTTTCAAGCTCCCA[A/C]AATAATTCCTCTAGT | 55230 |
rs370494116 | snp | C/T | | | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475255 | GCAACCTCTGCTTCC[C/T]GGGTTCAGACGATTC | 55230 |
rs370505341 | snp | C/T | | | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233488240 | GGAGAATTTCTTACC[C/T]CAAGTTTTCGCCTTT | 55230 |
rs370513057 | snp | A/C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233480404 | GGGGGCCTCTGGTGA[A/C/G]GCCTGCATGGAGCTG | 55230 |
rs370520616 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233499385 | TGGTATATATGTACC[A/G]TATTTTCTTTATCCA | 55230 |
rs370552737 | snp | C/G | 0.000329945 | 0.0128399 | intron-variant | USP40 | GRCh38.p7 | 2:233481183 | GTCAGCTGCACATCT[C/G]TGCAGACCCCAGCAA | 55230 |
rs370563213 | in-del | -/GAG | | | intron-variant | USP40 | GRCh38.p7 | 2:233514345 | GGTCAGGGATGAAAG[-/GAG]AAGGAACATCTCATA | 55230 |
rs370576744 | snp | A/C | 0.000325947 | 0.0127619 | intron-variant | USP40 | GRCh38.p7 | 2:233540611 | CATGTTGTTGCGATC[A/C]TAATGAAATTTCTTG | 55230 |
rs370592119 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233537473 | AAAAATACTTAGCAA[C/T]AGAATGTAAATAAAC | 55230 |
rs370603247 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233552212 | TCTAGTGGGTAAAAA[A/G]AAAAGTTGAATGAAA | 55230 |
rs370630141 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233516036 | TGTAAATATTTTAGG[C/T]TTCACGGGCCACATG | 55230 |
rs370679620 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233507482 | ATACACAACAGGGTA[A/C]TATTCAGCCATAAAA | 55230 |
rs370701511 | snp | A/G | 7.307e-05 | 0.00604398 | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233561230 | GAAAATAAAGTTCAT[A/G]TGGAACCAAAAAAGA | 55230 |
rs370709451 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476713 | TGGACCCTTGGCCTG[C/T]GGGCTGACGTGCAGC | 55230 |
rs370749840 | snp | G/T | 1.69063e-05 | 0.00290738 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233493479 | AAGTACAGTTGGTCT[G/T]GTCCTGATGACTCTC | 55230 |
rs370825157 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233497088 | AAATGAGAAACTGAT[A/T]TACAGAAGATGAAAT | 55230 |
rs370919210 | snp | A/G | 0.000106069 | 0.0072817 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233521087 | CTCATTCATACTAGT[A/G]ACCCATTTCTCTTCC | 55230 |
rs370937462 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233529596 | AAGACTAGGAAGGAC[A/T]GTCCTAGGAGCTAGG | 55230 |
rs370958725 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233480080 | GCAGCCTCTAACCAC[A/G]CTCGAACCCCCACTT | 55230 |
rs371081391 | snp | C/G | 0.000327946 | 0.012801 | intron-variant | USP40 | GRCh38.p7 | 2:233499965 | TGTTTCTGAGTTACA[C/G]TTCTAGGACAAACAC | 55230 |
rs371089198 | snp | C/T | 0.000169986 | 0.00921758 | intron-variant | USP40 | GRCh38.p7 | 2:233554550 | GACATGAATATAATA[C/T]TGAAAAACAATTTCA | 55230 |
rs371103224 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233560306 | CCAGGCACAATACTG[C/T]ATCTCGCTCTGGAGT | 55230 |
rs371106634 | snp | A/C | 8.30599e-05 | 0.00644384 | intron-variant | USP40 | GRCh38.p7 | 2:233529415 | TAGTCAAACTCTAAA[A/C]GCAATTTAAAATTAC | 55230 |
rs371128453 | in-del | -/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233489017 | AAATGACCCAAACCT[-/G]CTCTTTAAGTTCAAA | 55230 |
rs371263209 | snp | C/T | 5.17719e-05 | 0.00508756 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551377 | AAAATAGTTCAAACC[C/T]GTTCACAAAAGGGCT | 55230 |
rs371298437 | snp | C/G | 3.32579e-05 | 0.00407773 | intron-variant | USP40 | GRCh38.p7 | 2:233557030 | ATTTCCTACAAAACA[C/G]GTAACTTTTAGATGT | 55230 |
rs371299463 | in-del | -/ATAA | | | intron-variant | USP40 | GRCh38.p7 | 2:233536273 | AAATGTACACTTTAA[-/ATAA]GAGCTAAGTGGAAAG | 55230 |
rs371322461 | snp | C/T | 2.49791e-05 | 0.00353397 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485883 | GGGAGCCGGCAGTCC[C/T]ACCCTGGGCCGCGTT | 55230 |
rs371332163 | snp | A/G | | | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233493458 | TCCAAACTCTGCCCC[A/G]AGACGAAGTACAGTT | 55230 |
rs371333820 | snp | C/T | 1.66145e-05 | 0.00288218 | intron-variant | USP40 | GRCh38.p7 | 2:233540654 | CCCAAAACGATGCCA[C/T]GTATTACCTTCCGCA | 55230 |
rs371336622 | snp | A/G | 0.000167986 | 0.00916322 | intron-variant | USP40 | GRCh38.p7 | 2:233521137 | TAAAAAGAAAAGATC[A/G]GAAATTAATACCTTT | 55230 |
rs371348548 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233532238 | ATGGGTGTTGCCTGC[A/T]GCCAATCAGACTGAT | 55230 |
rs371363724 | snp | C/T | 1.66452e-05 | 0.00288484 | intron-variant | USP40 | GRCh38.p7 | 2:233540646 | TAGGACTTCCCAAAA[C/T]GATGCCATGTATTAC | 55230 |
rs371377702 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP40 | GRCh38.p7 | 2:233519427 | GAGGAGAACACAGGG[A/G]ACTTTAACTTCATTT | 55230 |
rs371380200 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | USP40 | GRCh38.p7 | 2:233506073 | GAACAGAGCTGGAGG[A/C]ACCATACTGCCTTAC | 55230 |
rs371394780 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233534099 | AACAAACACTTTTGA[A/C]ATATTTAAAAGCAAT | 55230 |
rs371456071 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233494987 | ATATATATACACACA[A/C]ATAAAAAATAAATAA | 55230 |
rs371475549 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233517091 | GTTGCTGGTAGGTAA[A/C]AAGGCAATGAATTTC | 55230 |
rs371510633 | in-del | -/T/TT | 0.239037 | 0.24976 | intron-variant | USP40 | GRCh38.p7 | 2:233518209 | TGTGCTCAAAATATG[-/T/TT]TTTTTTTTTTTAAAA | 55230 |
rs371553738 | snp | A/G | 0.000100487 | 0.00708757 | intron-variant | USP40 | GRCh38.p7 | 2:233491279 | TCCAAAGGACAGAGC[A/G]GGATGTTTACAAGGA | 55230 |
rs371567492 | snp | C/T | 0.000224723 | 0.0105977 | intron-variant | USP40 | GRCh38.p7 | 2:233485486 | ATAAAATCATGTGAC[C/T]CTCGTGTCTTCTCAA | 55230 |
rs371578318 | snp | C/T | 1.65701e-05 | 0.00287833 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233540694 | GCTGTTTTCTGTACT[C/T]CTTGTTCCAAGATAT | 55230 |
rs371580596 | snp | C/T | 3.50883e-05 | 0.00418843 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233510127 | CCCCATTGCAAAAAA[C/T]AGGAACAACTAATAA | 55230 |
rs371587688 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | USP40 | GRCh38.p7 | 2:233478007 | CGGCAGGTGCTCTGC[A/G]GCCGGGTGCTTTGGC | 55230 |
rs371599021 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233515434 | GGGTGCACAGTAGGG[C/T]GTCATTTGGTTTTAA | 55230 |
rs371631269 | snp | A/C | 0.000405091 | 0.0142261 | intron-variant | USP40 | GRCh38.p7 | 2:233524578 | CTAGAAAGAGATCAC[A/C]AGTGAGACCATTCAT | 55230 |
rs371642670 | snp | G/T | 1.6615e-05 | 0.00288223 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556897 | TTTACAAACAATCTG[G/T]TTAACAATGGTTCCA | 55230 |
rs371690551 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233557586 | ATTTATAACCAAACC[A/G]AGGGGCACACCAAGA | 55230 |
rs371697187 | snp | C/T | 7.92613e-05 | 0.00629479 | intron-variant | USP40 | GRCh38.p7 | 2:233489338 | AGCAGCAGAGAGGGA[C/T]AGTGTTGCGTCCAGC | 55230 |
rs371704970 | snp | A/G/T | 1.74595e-05 | 0.00295456 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485520 | GGTAAATTTGCTGTT[A/G/T]AACAACTTACCTTAA | 55230 |
rs371728345 | snp | C/T | 0.00013263 | 0.00814233 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233540764 | AGGAATTAGATTATT[C/T]TCCTCCTTATGAGAG | 55230 |
rs371785817 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476857 | AGACGTGGAGCATGC[A/G]GGGCCGGAACGAGTG | 55230 |
rs371787454 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476600 | AGCCCTGCCTGCCCC[A/G]CTTCCACACAGGAAG | 55230 |
rs371803568 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233511133 | TATGATTTCTGCACT[A/G]TAATAAGCTGATTAG | 55230 |
rs371823130 | snp | C/T | 0.000182266 | 0.00954461 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523226 | ATTTCTGAGCCCTTG[C/T]TCCCTGAACGTCTTC | 55230 |
rs371831691 | snp | C/G | 1.68727e-05 | 0.00290449 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477421 | CCACGTGGATGGAGA[C/G]AGAAGTTTCCGGGGC | 55230 |
rs371835340 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233510392 | TACTTCTTTTTCTTT[C/T]TTTTTTTTTTTTTTT | 55230 |
rs371840882 | snp | A/C | 7.43688e-05 | 0.00609745 | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233529549 | AACTTGTGTTGGCTA[A/C]ATGAAATCTGGTTGC | 55230 |
rs371846425 | snp | C/T | 4.98865e-05 | 0.00499407 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233496770 | TACCAGAGGAGGAAG[C/T]TGTCCTTCAATTAAA | 55230 |
rs371854716 | in-del | -/TT | | | intron-variant | USP40 | GRCh38.p7 | 2:233493385 | TCAATTTACTTCTCT[-/TT]ATGATGCACTGGCTG | 55230 |
rs371882975 | snp | A/C | 3.53163e-05 | 0.00420201 | stop-gained, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485934 | GGGCATAGGTCCTCT[A/C]ACCAGGGATGCGCAC | 55230 |
rs371919641 | snp | C/T | 2.69219e-05 | 0.00366882 | stop-gained, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485900 | CCCTGGGCCGCGTTC[C/T]ACACCAGGTCCAGGG | 55230 |
rs371923245 | snp | C/T | 1.95391e-05 | 0.00312556 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551448 | CTTGTAGCGTTCGCA[C/T]TTCACAAAATCAAAA | 55230 |
rs371953017 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233526114 | ACCAAAATAATATCA[C/T]CATAAAAGTCATTCC | 55230 |
rs371971779 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233494013 | TTTCAGTTTTACTTA[C/T]TTAGCTAGTTCTTCC | 55230 |
rs372075127 | snp | C/T | 4.97187e-05 | 0.00498567 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556922 | GTTCCATGGTACAGA[C/T]GATAGATGAGGTCAT | 55230 |
rs372120445 | snp | A/G | 0.000167986 | 0.00916322 | intron-variant | USP40 | GRCh38.p7 | 2:233511682 | GGAAGGGTTGATTTT[A/G]TTTTGAAACAGGTGA | 55230 |
rs372128530 | snp | C/T | 0.000400347 | 0.0141426 | intron-variant | USP40 | GRCh38.p7 | 2:233525443 | AAAAATGTAGATATA[C/T]AGAGTGAGTTGCTAT | 55230 |
rs372166118 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233531162 | AGAGCTACCTTACCA[C/T]GGATTAAAACACAAA | 55230 |
rs372185660 | in-del | -/TTT | | | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475383 | AGCCAGGCTGGTTTT[-/TTT]ACACTCCTGACCTCA | 55230 |
rs372202248 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233490697 | TGTGAACGTTAATGC[A/G]TAAGAAACAACACAA | 55230 |
rs372317045 | snp | A/T | 0.000169986 | 0.00921759 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233529461 | TCAATGTTAGCTGCA[A/T]CCATTTCATTCAGTA | 55230 |
rs372356341 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233489078 | ATTTCTGAGTGAGAA[A/C]CAGCCACTCCTACTT | 55230 |
rs372376905 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233494937 | ATATATATATATATA[C/T]ATATATATATATATA | 55230 |
rs372429090 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP40 | GRCh38.p7 | 2:233526797 | CTTTAAATCACACTG[C/T]CTCAACTTCAAAATG | 55230 |
rs372439391 | snp | A/G | 8.80553e-05 | 0.00663475 | intron-variant | USP40 | GRCh38.p7 | 2:233519604 | CCGAAAAGAAAATGT[A/G]AATGATTACCTAGTT | 55230 |
rs372446647 | snp | A/C/G | 3.33474e-05 | 0.00408323 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233493430 | CTGTTCTCACCTTGG[A/C/G]TGGAAGTGGCTCTCC | 55230 |
rs372448712 | snp | C/T | 0.000103557 | 0.00719499 | intron-variant | USP40 | GRCh38.p7 | 2:233542390 | AACAGTATGAGTTTC[C/T]ATCACTAACCCCTTA | 55230 |
rs372470147 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233509315 | AGGTCTCAGTTCTCA[A/G]TAACAGCAATATAAT | 55230 |
rs372538075 | snp | G/T | | | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233567257 | TGATCTTATATAAGA[G/T]TATAGCTATATGATC | 55230 |
rs372617738 | snp | C/T | 2.21732e-05 | 0.00332958 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533771 | TATCTGAGAATGGAG[C/T]TGTAAGAACTACACA | 55230 |
rs372624319 | snp | A/G | 3.36831e-05 | 0.00410371 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233498588 | TCATAGCACCAATCC[A/G]TTTTTCGTAAATGCC | 55230 |
rs372648019 | snp | C/G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233532062 | AGGAAATTGGCTGAC[C/G/T]CCAACGAATCAGACA | 55230 |
rs372680595 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP40 | GRCh38.p7 | 2:233538644 | AACTTCATACTGAGA[C/T]ACACATGTATAAGAA | 55230 |
rs372751073 | in-del | AA/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233516332 | GTCAATTTCTTTAAA[AA/G]ATGTTAAGATTCTGT | 55230 |
rs372770552 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233509765 | AGAATCACTTGAACC[C/T]GGGAGGCAGAGGTTG | 55230 |
rs372778386 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233528660 | TCTGTTAAGTTTTAA[A/T]CTTTTTGGTATCTTG | 55230 |
rs372797472 | snp | A/G/T | 1.97482e-05 | 0.00314225 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233493536 | GGTACCACCAGATGG[A/G/T]CACCTTCAGGAAACC | 55230 |
rs372802035 | snp | C/T | | | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233488265 | GCCTTTCTGAAGGGG[C/T]TCTAAGCAGATCTCA | 55230 |
rs372824643 | snp | A/C/G | 0.000224871 | 0.0106016 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477385 | GTAGAGCCGTGCAGC[A/C/G]GCGCGGTTATCTGAA | 55230 |
rs372849264 | snp | C/G | 9.31576e-05 | 0.00682423 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233549107 | TATACGTACTTGAAA[C/G]TGCCAGTTTCCCAAA | 55230 |
rs372916577 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233508779 | AAAATGCTTTATTTT[C/T]TACCTTTATGATTGC | 55230 |
rs372939161 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233498889 | ATTCCGTCATCTATA[C/G]CACAAAAATACTGAC | 55230 |
rs372943765 | snp | C/T | 1.6784e-05 | 0.00289685 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527497 | AGAGACTACTGGGTG[C/T]AGAGCCCCATTGAAG | 55230 |
rs372947779 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233558689 | ATTGATTGTAGTGAT[A/G]GTTGAACAACTCTGT | 55230 |
rs372952253 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233558825 | TGTTAATCGGATTAA[C/T]GCCAAATACCAGCCC | 55230 |
rs372976877 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233522665 | ACAGGATTCATGGGG[G/T]TAATTCGCCACGTAA | 55230 |
rs372981440 | snp | A/C | 1.88848e-05 | 0.00307279 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485756 | TCTCTGAGACAGCCC[A/C]ACAACTTTACCCAGC | 55230 |
rs372993331 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233551861 | ACCTGGCAGGTCTAC[A/G]GTTCTTTTTAATCAG | 55230 |
rs373065897 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233494959 | ATATATATATATTTA[A/T]ATATATATATATATA | 55230 |
rs373111998 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476059 | ACGTCTATGGCAGAC[A/G]CTCTCAGACACGTGT | 55230 |
rs373118902 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233507060 | ATGGCCAACAGGTAC[A/G]CACACAAAAAATGCT | 55230 |
rs373138331 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233568583 | ATATCTTTGTCTTTC[A/G]TCTGTGAATCAAACT | 55230 |
rs373145165 | snp | G/T | 0.00636936 | 0.0560724 | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475186 | TATTTTTTTTGAGAC[G/T]GAGTCTCGCTCTGTC | 55230 |
rs373146800 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233494947 | ATATATATATATATA[A/T]ATATATATTTATATA | 55230 |
rs373147313 | snp | A/T | 1.65831e-05 | 0.00287945 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233554456 | ACTTCCTCTTCTACA[A/T]ACATGTTCCAGAGAG | 55230 |
rs373156583 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233509530 | ATAGAAAGAAAAAAA[C/T]TGTAATCTTATTTAA | 55230 |
rs373185551 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | USP40 | GRCh38.p7 | 2:233517859 | GCCATAAAAAGGAAT[G/T]AATTAATGGCATTTG | 55230 |
rs373209416 | snp | C/T | 0.000298085 | 0.0122047 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233511793 | CAAAGTATAGCTGTC[C/T]GGCACTTAAAAAAAT | 55230 |
rs373226220 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527435 | TGCCGGAGATCTCCT[A/G]AAGTTTTTCTTTTAT | 55230 |
rs373260871 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233505020 | ATTTTTTCTAACCAC[A/G]ATAAAACTAGAAATC | 55230 |
rs373276730 | snp | A/G | 1.83008e-05 | 0.00302491 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485631 | ATTTGTTGGTTCTAT[A/G]GGAAAATCAAACATC | 55230 |
rs373280200 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233540585 | TTTAAATATCCTTCT[A/G]CAAAGGAATTCATGT | 55230 |
rs373282433 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233475564 | TTTTTTCTTTAACAA[A/G]ATCGTACAGCTTTCT | 55230 |
rs373327166 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP40 | GRCh38.p7 | 2:233555497 | TATATACGTGAAAAG[C/T]TAATGTCTTTAATTT | 55230 |
rs373340316 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233492208 | GATTCGCCTTCAGTA[C/T]TCAATACAGTAAGCT | 55230 |
rs373402622 | snp | C/G | 1.65784e-05 | 0.00287905 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533609 | TATATCAAACCAGTG[C/G]GGACAGGAGATGCTA | 55230 |
rs373457318 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | USP40 | GRCh38.p7 | 2:233492651 | ACTTCAAAGAATAAG[A/G]AGATAAGAATTTGAC | 55230 |
rs373474102 | snp | A/G | 3.39081e-05 | 0.00411739 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477470 | CTCTGCACTGGAGAG[A/G]ATGTAGCTGCTCTGC | 55230 |
rs373545594 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233491656 | TGTCTGTGTGCAGGC[A/G]TTTAATCTGCCTCCT | 55230 |
rs373555933 | snp | A/G | 6.63207e-05 | 0.00575812 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533518 | ATTTCCGATAAAACA[A/G]CATGTAGGCACTTTC | 55230 |
rs373556308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233545215 | AATAAGTATGTTTAA[A/G]GTGCTTGAAGAAATT | 55230 |
rs373560963 | snp | G/T | 0.000105266 | 0.00725411 | intron-variant | USP40 | GRCh38.p7 | 2:233521146 | AAGATCAGAAATTAA[G/T]ACCTTTCCTTAGGCA | 55230 |
rs373580250 | snp | C/T | 0.021333 | 0.101051 | intron-variant | USP40 | GRCh38.p7 | 2:233479375 | TGAGACCATCCTGGC[C/T]AACATGGTGAAACCT | 55230 |
rs373599460 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233555659 | TTTTTTTTTTTGAGA[C/T]GGAGCCTTGCTCTGC | 55230 |
rs373605894 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233538101 | ATTTGTAATTTATCA[C/T]GTTAATTTATATATA | 55230 |
rs373655001 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233537704 | GATTAACTTATAATT[C/T]TGTATCTATCAAAAA | 55230 |
rs373719433 | snp | A/T | 3.22232e-05 | 0.0040138 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233559923 | AAAGGGATGATTCGA[A/T]CCTGAATGAGAAACA | 55230 |
rs373726818 | in-del | -/GT | 0.4862 | 0.0819127 | intron-variant | USP40 | GRCh38.p7 | 2:233517782 | GATAAAGAAACTGTG[-/GT]GTGTGTGTGTGTGTG | 55230 |
rs373752618 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233533464 | AAACAAATAGGAACA[C/T]TTTTCTTTCCATACC | 55230 |
rs373777737 | snp | C/T | | | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523485 | TGAATGTGGACTCCA[C/T]CAACCTGCAATCATA | 55230 |
rs373777790 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233478049 | TGTGTGGCCCACCCA[C/T]GCTGCACAGTCCCCG | 55230 |
rs373781675 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233494592 | GATTTTTGGCTGGGC[G/T]TGGTGGCTCACAGCT | 55230 |
rs373786382 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233542099 | ACCAGAAAATCCCCA[A/C]AAACATCATTAAAAT | 55230 |
rs373814294 | snp | A/C/G | 0.00013742 | 0.00828811 | intron-variant | USP40 | GRCh38.p7 | 2:233527388 | ATGTCTGAATTAAGA[A/C/G]GAAGTAAGGCGATAT | 55230 |
rs373837089 | snp | A/G | 8.31774e-05 | 0.00644839 | intron-variant | USP40 | GRCh38.p7 | 2:233489320 | CACACCAGCCAGTGC[A/G]TCAGCAGCAGAGAGG | 55230 |
rs373843017 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233493601 | CAAAGATTAAGTGAA[A/G]CTCTACTTTTACTTC | 55230 |
rs373868010 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233548602 | GGGAAAAATTGCCAT[A/G]AAGGATGTGAACTGG | 55230 |
rs373869048 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562846 | CAAATGACATCATTT[C/T]ATTTTAAAAAATTGT | 55230 |
rs373901889 | snp | A/C | 0.000169986 | 0.00921759 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551470 | AAATCAAAATTAAAT[A/C]TTAGTAATGAAACAG | 55230 |
rs373950047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233480554 | GCCTGTGGCTTGGCC[C/T]GACTGCAAGCAGCAC | 55230 |
rs373970733 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233521269 | TGCAGGGTAATGTTA[A/G]GCAGTAGTCTATAGA | 55230 |
rs373992248 | snp | C/T | 0.000181989 | 0.00953737 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477353 | GTTTGTGGCATCAGC[C/T]GGAGAGTTCATCGGG | 55230 |
rs373996763 | snp | A/C | 4.57038e-05 | 0.00478015 | intron-variant | USP40 | GRCh38.p7 | 2:233527590 | TGCCCTTTAAAGAGG[A/C]ACAAAAATACATAAA | 55230 |
rs374005547 | snp | G/T | 1.68681e-05 | 0.00290409 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233493475 | GACGAAGTACAGTTG[G/T]TCTGGTCCTGATGAC | 55230 |
rs374034379 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233564472 | CAGAGATGGGGTATG[A/G]GAGAAATATATAGAG | 55230 |
rs374056462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233488188 | GCTTCAAAAGGCAAA[C/T]GAGGTTAAGATACGT | 55230 |
rs374074241 | snp | A/T | 5.17335e-05 | 0.00508567 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523463 | AGGTTCGCAGTCAAT[A/T]CCAGTTTGAATGTGG | 55230 |
rs374106216 | snp | C/T | 0.000291634 | 0.012072 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485895 | TCCCACCCTGGGCCG[C/T]GTTCCACACCAGGTC | 55230 |
rs374139381 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233515255 | AGTAAATACCTAGAC[A/G]TAGAATTGGTAAGTG | 55230 |
rs374145374 | snp | C/T | 0.000145497 | 0.00852803 | intron-variant | USP40 | GRCh38.p7 | 2:233489350 | GGACAGTGTTGCGTC[C/T]AGCAAGGAACCTACC | 55230 |
rs374157100 | snp | A/T | 0.000306315 | 0.0123719 | intron-variant | USP40 | GRCh38.p7 | 2:233524598 | AGACCATTCATCATG[A/T]CCATCAGAAACAACT | 55230 |
rs374202390 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233501552 | GAAATTCATTTCAGA[A/T]GAAAAAGATGACAGG | 55230 |
rs374208509 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543317 | TTACTAAAAATGCTA[A/G]ATAAAGTAAAACCAA | 55230 |
rs374226773 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233530762 | AATTGCTTATTTATA[C/T]CATTTCCCCAATTTA | 55230 |
rs374310033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233553819 | CTCACATGGCAAAAG[A/G]TATCAGTTGCTTCAG | 55230 |
rs374322158 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233537296 | TGAGCATCTGCAGAT[A/G]TGGGTGTCATCTGGG | 55230 |
rs374326845 | snp | C/T | 6.49583e-05 | 0.00569868 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233529450 | TGGTTTGCAGTTCAA[C/T]GTTAGCTGCATCCAT | 55230 |
rs374363326 | in-del | -/ATATA | | | intron-variant | USP40 | GRCh38.p7 | 2:233533336 | ATTTCATTTGGCATA[-/ATATA]GTTCTTGTTAGCTTT | 55230 |
rs374377490 | snp | C/G/T | 0.000389535 | 0.0139514 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477377 | CATCGGGAGTAGAGC[C/G/T]GTGCAGCGGCGCGGT | 55230 |
rs374388511 | snp | C/T | 0.000167986 | 0.00916322 | splice-donor-variant | USP40 | GRCh38.p7 | 2:233556854 | ACTCTGGCATATTTA[C/T]CTGCCTCTCGCTAAC | 55230 |
rs374465920 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233494989 | ATATATACACACACA[A/T]AAAAAATAAATAAAT | 55230 |
rs374491288 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233556803 | ATACATTTAATTACA[C/T]GGATTATAATTTACA | 55230 |
rs374496721 | snp | C/T | 0.0588605 | 0.161139 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233567768 | TATATAAGATTATAG[C/T]TATATAACCTTATAT | 55230 |
rs374508674 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233544020 | CAGGTGACAGCACAG[A/G]CTCCATAAGTTGAGG | 55230 |
rs374546325 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233524382 | TGATCTGCCTGCCTC[A/G]CCCTCCCAAAGTGCT | 55230 |
rs374569235 | snp | C/T | 5.20061e-05 | 0.00509906 | intron-variant | USP40 | GRCh38.p7 | 2:233488336 | CAAGATAATATTGAG[C/T]GACATAACATTTAAT | 55230 |
rs374578540 | snp | C/G | 0.000138545 | 0.00832186 | intron-variant | USP40 | GRCh38.p7 | 2:233554552 | CATGAATATAATATT[C/G]AAAAACAATTTCAGA | 55230 |
rs374587907 | in-del | AA/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233488911 | GACCCTGTCTATTAA[AA/G]AAAAGAAAGAAAAGG | 55230 |
rs374623371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233479920 | GGGCCGTGCTGCTTG[C/T]GGAGCTCACACAGTC | 55230 |
rs374625248 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233554261 | AGAAAATGATGTAAA[C/T]ATCTTTTCAATCCTT | 55230 |
rs374687398 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233537615 | AATAAAAAATGACAG[C/T]TGGCTTCTCATCCAA | 55230 |
rs374697846 | snp | A/G | 0.000102513 | 0.00715864 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551389 | ACCTGTTCACAAAAG[A/G]GCTTGAGATTAATCC | 55230 |
rs374741823 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233519040 | GTTTTATGATTCCAA[C/T]TACATTAAACATTAA | 55230 |
rs374744940 | snp | A/C | 1.67503e-05 | 0.00289393 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523189 | TATCATCATGAGAAT[A/C]CTGAATTAAAATTGA | 55230 |
rs374758816 | snp | A/G | 0.000101107 | 0.00710938 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233510106 | TGTCCCAGGTTGAAC[A/G]TCACTCCCCATTGCA | 55230 |
rs374779930 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233527861 | TTCTAATTCTGAGAT[G/T]ATATTATAGTTATGA | 55230 |
rs374878010 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233563549 | TAAGTGCTGGGACTC[A/G]GCAAAAATGAACTAC | 55230 |
rs374907901 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233548916 | ACTATTCTGGTAATT[C/T]TTCTGTATGTGTGAA | 55230 |
rs374987705 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233493860 | ACCAGCGTTTCCAGG[A/C/T]GCTGTCCAAGCACTG | 55230 |
rs375019524 | snp | A/T | 3.35014e-05 | 0.00409262 | intron-variant | USP40 | GRCh38.p7 | 2:233540613 | TGTTGTTGCGATCAT[A/T]ATGAAATTTCTTGGG | 55230 |
rs375020351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233508568 | TTCTGAATTTCTATG[C/T]TGTCTGAGTGTTGCT | 55230 |
rs375068746 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233479661 | TGTGTGTGTGTGTGT[C/G]TGACCTTTAAACAGG | 55230 |
rs375072962 | snp | C/T | 8.30496e-05 | 0.00644344 | intron-variant | USP40 | GRCh38.p7 | 2:233481191 | CACATCTGTGCAGAC[C/T]CCAGCAATTACCTTT | 55230 |
rs375078937 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233482003 | CGCTGGCTGCATTCT[C/G]AGGTGTGGAGGTGGG | 55230 |
rs375114020 | in-del | -/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233509872 | AAAAAAATCCAGTTG[-/G]TTCACCAATTTTCAA | 55230 |
rs375200887 | snp | A/G | 0.000391452 | 0.0139847 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485935 | GGCATAGGTCCTCTC[A/G]CCAGGGATGCGCACC | 55230 |
rs375216964 | snp | A/G | 0.000169985 | 0.00921758 | intron-variant | USP40 | GRCh38.p7 | 2:233551540 | AAAAGAAAAATTTAC[A/G]AAGCTTTTTAAAAAC | 55230 |
rs375217340 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233490916 | AAAATGAACAAAAGC[C/T]GCAAGTCACTGAGGA | 55230 |
rs375223627 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233492348 | GATGAAATCATCTGA[C/T]GATGCATTTCTCAAA | 55230 |
rs375226593 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233517907 | TTGGAAACTATTATT[A/G]TAAGTGAAGTAACTC | 55230 |
rs375227387 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233511956 | TGCACTAAGATTAGG[C/T]TTGATTTTCAATTTC | 55230 |
rs375241300 | snp | C/T | 8.42779e-05 | 0.00649091 | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233561249 | AACCAAAAAAGAGCC[C/T]GCATCGCCAAGTCAA | 55230 |
rs375362377 | snp | C/T | 3.93252e-05 | 0.00443408 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485726 | ACCTCATTGCTATGC[C/T]GGTAAGCCCCAATTT | 55230 |
rs375363387 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233551068 | TCAGTGGTTCTCAAA[A/C]AGGGTCAATCTTGCC | 55230 |
rs375372505 | snp | C/T | 8.48428e-05 | 0.00651262 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233542279 | ATACCTCTAATAAGA[C/T]TGCTTTTAGAATCAT | 55230 |
rs375376271 | snp | A/G | 0.000125589 | 0.00792329 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233511794 | AAAGTATAGCTGTCC[A/G]GCACTTAAAAAAATT | 55230 |
rs375447050 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233550187 | ATTAAACTTTTTAAG[C/T]GGGCAGCATTTTAAA | 55230 |
rs375486252 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233554620 | GAATAATCAGATATA[C/T]GTTTTCTAAAACATT | 55230 |
rs375487129 | snp | A/T | | | splice-acceptor-variant | USP40 | GRCh38.p7 | 2:233542365 | TTACTTTTTTCCTCC[A/T]AGGAAGGAAAACAGT | 55230 |
rs375517784 | in-del | -/GTGTGTGTGTGTGT | | | intron-variant | USP40 | GRCh38.p7 | 2:233491622 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTGTGT]CTGTCTGTCTGTGTG | 55230 |
rs375523316 | snp | A/G | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233487415 | TTAACTATTTTAAGA[A/G]GTTTAAAATGTCCAC | 55230 |
rs375538171 | in-del | -/CT | 0.00318978 | 0.0398085 | intron-variant | USP40 | GRCh38.p7 | 2:233522395 | ATGTCTGCAAAACCC[-/CT]GTCCAAAAGAGTAAT | 55230 |
rs375552346 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233555489 | GTTTATAATATATAC[A/G]TGAAAAGTTAATGTC | 55230 |
rs375600870 | snp | C/G | 0.000321948 | 0.0126835 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477453 | CGGGGCCGGGCAGGC[C/G]TCTCTGCACTGGAGA | 55230 |
rs375687877 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233503640 | TAGGAAAGAAAAAAA[A/C]ACTGTCAGCCAAGAA | 55230 |
rs375700049 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233529899 | TCTGCCTCCCAGGTT[A/C]AAGCAATTCTCGTGC | 55230 |
rs375703858 | snp | C/T | 0.000117168 | 0.00765311 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233493462 | AACTCTGCCCCAAGA[C/T]GAAGTACAGTTGGTC | 55230 |
rs375704351 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476530 | GGCTACTCAGGAAAC[C/T]GGTCAGGCTGCCCAG | 55230 |
rs375708922 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233490146 | GAATAAGGCTGTCTG[C/G]TTTTTCTTTTCTCCT | 55230 |
rs375716263 | snp | C/T | 5.04503e-05 | 0.00502221 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527507 | GGGTGCAGAGCCCCA[C/T]TGAAGAAATGATACT | 55230 |
rs375722734 | snp | C/T | 0.000169986 | 0.00921758 | intron-variant, splice-donor-variant | USP40 | GRCh38.p7 | 2:233561159 | ATCATAGATGTAATA[C/T]CTTTGCATCGGGTTT | 55230 |
rs375726929 | in-del | -/G | 0.0107246 | 0.0724382 | intron-variant | USP40 | GRCh38.p7 | 2:233552225 | AAAAAAGTTGAATGA[-/G]AAAAAAAAAAACAAA | 55230 |
rs375764043 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233521558 | ATATATATTGTATAC[C/T]GCATTTCTACATAGA | 55230 |
rs375791080 | snp | C/T | 2.26027e-05 | 0.00336167 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485864 | TCGGCAACTCTCTGC[C/T]TCAGGGAGCCGGCAG | 55230 |
rs375792587 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233544715 | AATATATCACAATGA[A/C]AAAATCCGGCAAAAA | 55230 |
rs375802006 | snp | C/T | 0.000351938 | 0.0132607 | intron-variant | USP40 | GRCh38.p7 | 2:233549274 | ATAGTTTTCATAAAA[C/T]GCTGATAATAATCAA | 55230 |
rs375815235 | snp | C/T | 0.000149301 | 0.00863876 | splice-acceptor-variant | USP40 | GRCh38.p7 | 2:233521115 | TCCTTGGTCAACAAG[C/T]TGTAGGTAAAAAGAA | 55230 |
rs375836928 | snp | C/T | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233487036 | GGGCCTGAGGAGGCA[C/T]ACAGCTGCTCTTCAA | 55230 |
rs375857468 | snp | A/G | 4.97822e-05 | 0.00498885 | intron-variant | USP40 | GRCh38.p7 | 2:233559778 | CTTTCCTCTATTGCT[A/G]GTAACTCTTCCTTAA | 55230 |
rs375858803 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233494951 | ATATATATATATATA[A/T]ATATTTATATATATA | 55230 |
rs375877100 | snp | A/T | 2.22373e-05 | 0.00333439 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533772 | ATCTGAGAATGGAGC[A/T]GTAAGAACTACACAG | 55230 |
rs375898893 | snp | C/T | 5.24893e-05 | 0.00512268 | intron-variant | USP40 | GRCh38.p7 | 2:233510170 | GTAAATGCAATTTAA[C/T]CTGAATTTAAAAATC | 55230 |
rs375910922 | snp | G/T | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486744 | AAAGAGAGTTCACGG[G/T]AAGATGTGGGCCCAT | 55230 |
rs375955795 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233510270 | ATTTATATGAAAATA[C/T]GACTATGATTAATGT | 55230 |
rs375967403 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233484307 | ACTGATACCTTTACT[A/G]TTGTGAGGTTTGCCT | 55230 |
rs375987122 | snp | C/T | 9.70732e-05 | 0.00696615 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233562796 | TGGGCCAAGAGAAAA[C/T]AGAGCTTCTAAAGAA | 55230 |
rs376032732 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233555131 | CTGGGAGGCGGAGGT[C/T]GCAGTGAGCCGAGAT | 55230 |
rs376077546 | in-del | -/ATAA | | | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485651 | AATCAAACATCTTAA[-/ATAA]GCAAAACTCAACCTC | 55230 |
rs376135494 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233560407 | TGGGGCAGACTGAGC[A/C]ATGTTGCTCAGAGTC | 55230 |
rs376150492 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233544396 | CTGAAGTTTCATTAC[A/G]GAGGCATGACCGATT | 55230 |
rs376212595 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233564150 | ACCCATTAAATTGCT[C/G]CTAGGAAGGTAACAG | 55230 |
rs376262253 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233557705 | GAGGGTGGTGAGTGC[C/T]GCTGAGAGCTCCTTC | 55230 |
rs376266674 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233494963 | ATATATATTTATATA[A/T]ATATATATATATATA | 55230 |
rs376289973 | snp | A/G | 8.08506e-05 | 0.00635757 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551507 | AAGGAGGCAGCTTAC[A/G]TAATTTGGCCGACTG | 55230 |
rs376313691 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233515092 | TGGAACTAGCAGTGC[C/T]TTGCTCTTCAGTGAC | 55230 |
rs376341226 | snp | C/T | 8.41531e-05 | 0.0064861 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485551 | CACCAATAGTATCTC[C/T]GTCTTTCAAGTAATA | 55230 |
rs376347714 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233559545 | AAGACTCTTAGGGTA[G/T]AAATTGTAAAAATCA | 55230 |
rs376401229 | snp | C/T | 0.000120111 | 0.00774861 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477389 | AGCCGTGCAGCGGCG[C/T]GGTTATCTGAAGCTC | 55230 |
rs376423021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233521666 | AAGAGGTGCCTTCTT[C/T]CTAATTCACACAGAA | 55230 |
rs376485446 | snp | C/T | 0.000169986 | 0.00921759 | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233529551 | CTTGTGTTGGCTAAA[C/T]GAAATCTGGTTGCTG | 55230 |
rs376498120 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233492710 | TGAAAAGATTAAAAA[C/G]AAATATAAGTAATAT | 55230 |
rs376529466 | snp | C/T | 0.000887532 | 0.021047 | intron-variant | USP40 | GRCh38.p7 | 2:233498518 | ATAAATGTAATCATA[C/T]GAAAGTACAATGTAT | 55230 |
rs376533938 | snp | C/T | 0.00456943 | 0.0475798 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477472 | CTGCACTGGAGAGGA[C/T]GTAGCTGCTCTGCTC | 55230 |
rs376618236 | in-del | -/CCA | | | intron-variant | USP40 | GRCh38.p7 | 2:233536452 | AAGAACAAAACACCA[-/CCA]GTCTGGCCAACATGG | 55230 |
rs376630586 | snp | A/G | 0.000253976 | 0.011266 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233489454 | CTGTTTTAGAAAAA[A/G] | 55230 |
rs376644531 | snp | C/G | 5.0078e-05 | 0.00500365 | intron-variant | USP40 | GRCh38.p7 | 2:233525589 | TAATGAAGGAAAAGA[C/G]AATGTTGAAAAGTGA | 55230 |
rs376650501 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233526119 | AATAATATCACCATA[A/C]AAGTCATTCCTATCT | 55230 |
rs376654718 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | USP40 | GRCh38.p7 | 2:233547094 | GAAATGGAAGGCAAA[-/G]GATTTGGACAGGTAA | 55230 |
rs376670354 | snp | C/T | 6.63658e-05 | 0.00576008 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233525478 | TCATATTTATCTTAC[C/T]GCCAAGTGACTGGTA | 55230 |
rs376677069 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233563548 | CTAAGTGCTGGGACT[C/T]GGCAAAAATGAACTA | 55230 |
rs376775598 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233494939 | ATATATATATATATA[C/T]ATATATATATATATA | 55230 |
rs376815690 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562430 | GGGACATGGATGAAA[C/T]TGGAAATCATCATTC | 55230 |
rs376822255 | snp | A/T | 0.000273322 | 0.011687 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233521071 | CGTGGAGCCAGTCAA[A/T]CTCATTCATACTAGT | 55230 |
rs376833819 | snp | C/T | 1.7107e-05 | 0.00292459 | intron-variant | USP40 | GRCh38.p7 | 2:233554369 | GGGAAAAAGCAGTTA[C/T]CTGTCTTTACCTTTG | 55230 |
rs376853811 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233523938 | AGTTCTTCACACGAC[A/G]AGGGCCTAAAAGGAC | 55230 |
rs376941461 | snp | A/G | 0.000165986 | 0.00910855 | intron-variant | USP40 | GRCh38.p7 | 2:233527399 | AAGAGGAAGTAAGGC[A/G]ATATTACCTGAAATA | 55230 |
rs376953955 | snp | A/G | 7.79008e-05 | 0.00624054 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233559839 | CACCCAAAGCTGTCA[A/G]TGAGGTCTGCTGTGG | 55230 |
rs376972355 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233507732 | GTCAACAGGTACAAA[A/G]TTACAATCTAATAGA | 55230 |
rs376984238 | snp | A/G | 8.78619e-05 | 0.00662746 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233519663 | TTTAATTCGAATATC[A/G]AACACCATCTAAAAC | 55230 |
rs376990550 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233563980 | TTTAACTTCAACTAT[A/G]TTAAAACCTGGAAAA | 55230 |
rs377058590 | snp | C/T | 3.68657e-05 | 0.00429319 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233488304 | TCCTAGTTTATATTC[C/T]CTGATAATAAGTGAA | 55230 |
rs377069665 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233528891 | GTGAGGCCCCAAAAG[A/C]GAATGCTGAGATCAT | 55230 |
rs377114171 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233555942 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAAAA | 55230 |
rs377155341 | snp | A/G | 1.65674e-05 | 0.00287809 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523412 | ACACTTTTCTCCATC[A/G]CTGCTTGTGTCTAGA | 55230 |
rs377190658 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233558236 | TACCACTGCAGGTCC[A/G]GTCCTAGAGGGTTTT | 55230 |
rs377196330 | in-del | -/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233531639 | AATACAAAGCCTTTT[-/T]CATTAACAGCATAGT | 55230 |
rs377252042 | snp | A/T | 0.000171985 | 0.00927163 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233549203 | TGAGAAGAGGTCATA[A/T]ATATATTCTAAGTCA | 55230 |
rs377293718 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233537409 | AATTGAAGAAATAAT[A/G]GCCAAAATTTTTCCA | 55230 |
rs377384049 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233484053 | CGCCACAGCTGTGAT[A/C]AGTCAACACTTGGTG | 55230 |
rs377389858 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233551879 | TCTTTTTAATCAGTG[A/G]AGAACTGGAGCTCTT | 55230 |
rs377392332 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233522152 | GTCTACAAATCTCAA[A/G]GTTGGGCAGGGGTAA | 55230 |
rs377440642 | snp | A/T | 0.000167986 | 0.00916323 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527439 | GGAGATCTCCTAAAG[A/T]TTTTCTTTTATCAAA | 55230 |
rs377485271 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233566725 | GCCAAAACGCGAAGC[C/G]AACGAACCCGCCCCA | 55230 |
rs377486799 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233522888 | TTCACTTGATAACTT[C/T]TGCATTACAGCCAAC | 55230 |
rs377522114 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233566685 | CCAGCCGCACTTACT[A/G]CCTAAAGCCCAGACC | 55230 |
rs377522297 | in-del | -/TGGAACCAA | | | intron-variant | USP40 | GRCh38.p7 | 2:233517732 | GCAATTGCAAAATCA[-/TGGAACCAA]CCCAAATGCCCATCA | 55230 |
rs377528949 | snp | A/G | 0.000165986 | 0.00910855 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486000 | AGAAAACCGTCAAGC[A/G]CCAGATCCAAACAAA | 55230 |
rs377532878 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP40 | GRCh38.p7 | 2:233503885 | GAATACCCCAGTGTC[A/G]CAATGGTGCTATATA | 55230 |
rs377598747 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233540152 | AACAAAAAACAAACC[-/A]AAAAAAAAACTTGAT | 55230 |
rs377604509 | snp | A/G | 6.1393e-05 | 0.0055401 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485842 | CTCCACGGGAAGACG[A/G]TAGAAATCGGCAACT | 55230 |
rs377615770 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233515988 | TTGAAAGTCAATGAC[C/T]ACGCACCTATTTCTA | 55230 |
rs377650534 | snp | C/T | 0.000122306 | 0.00781908 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523468 | CGCAGTCAATACCAG[C/T]TTGAATGTGGACTCC | 55230 |
rs377653761 | snp | A/T | 5.14064e-05 | 0.00506957 | intron-variant | USP40 | GRCh38.p7 | 2:233554538 | CTTCCTGAAATAGAC[A/T]TGAATATAATATTGA | 55230 |
rs377701272 | snp | A/G | 1.97315e-05 | 0.00314091 | intron-variant | USP40 | GRCh38.p7 | 2:233521130 | CTGTAGGTAAAAAGA[A/G]AAGATCAGAAATTAA | 55230 |
rs377725292 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233499165 | CCCACTCCCACCCCC[C/G/T]CATACACCAACAGGC | 55230 |
rs377727549 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233517855 | CTCAGCCATAAAAAG[G/T]AATGAATTAATGGCA | 55230 |
rs377744344 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233494992 | TATACACACACATAA[A/T]AAATAAATAAATAAA | 55230 |
rs386656353 | multinucleotide-polymorphism | AAC/GAA | | | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475149 | GGAAAAAGGGCCACA[AAC/GAA]GTTCCTTATTTTATT | 55230 |
rs386656354 | multinucleotide-polymorphism | CA/TG | | | intron-variant | USP40 | GRCh38.p7 | 2:233478790 | GGTACATGAAAACAG[CA/TG]AGGTTACCAAGAAAG | 55230 |
rs386656355 | multinucleotide-polymorphism | CA/TG | | | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485922 | GGTCCAGGGCAGGGG[CA/TG]TAGGTCCTCTCACCA | 55230 |
rs386656356 | multinucleotide-polymorphism | AC/CT | | | intron-variant | USP40 | GRCh38.p7 | 2:233538510 | ATAAGTTCATATTCT[AC/CT]AGTCACTAAACGGAT | 55230 |
rs397717843 | in-del | -/T | 0 | 0 | intron-variant | USP40 | GRCh38.p7 | 2:233549652 | GCATCCCCTTTTTTT[-/T]ATTGATATATATCTA | 55230 |
rs397798564 | in-del | -/T | | | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233529601 | AGGAAGGACTGTCCT[-/T]AGGAGCTAGGAAAGC | 55230 |
rs397953463 | in-del | -/TCT | | | cds-indel, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233521097 | TAGTGACCCATTTCT[-/TCT]CTTCCTTGGTCAACA | 55230 |
rs397971707 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233478994 | AACTCCAAAAAAAAA[-/A]TGAAAAACAATATAG | 55230 |
rs397988270 | in-del | -/T | 0 | 0 | intron-variant | USP40 | GRCh38.p7 | 2:233556298 | TTCCAATTTCTAATT[-/T]CCAATTAGATTAAAT | 55230 |
rs398081153 | in-del | -/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233556297 | TTTCCAATTTCTAAT[-/T]TCCAATTAGATTAAA | 55230 |
rs527240049 | snp | G/T | | | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233489372 | GAACCTACCTGAGTG[G/T]CTGCCGGTCAGTTCG | 55230 |
rs527253869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233564318 | TCTGTCCTCCTAATA[C/T]GGAGACACTGTGGAG | 55230 |
rs527269974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233519813 | CCACTGGAAATTTTT[C/T]CATCCCTGAAATCCT | 55230 |
rs527285148 | snp | A/C/T | 3.45496e-05 | 0.00415618 | intron-variant | USP40 | GRCh38.p7 | 2:233520965 | CTGAAAATCTATCAG[A/C/T]CAACCTTTAATTATA | 55230 |
rs527293503 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233512394 | TTAGAAAACAGAAGT[C/G]TTTGTTTCTGGTTAA | 55230 |
rs527365672 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475454 | CAGGCGTGAGCCACC[A/G]CGCCCGGCCAAAAGT | 55230 |
rs527366660 | snp | C/T | 3.36939e-05 | 0.00410436 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556869 | CCTGCCTCTCGCTAA[C/T]GTTCTTACATTCTTT | 55230 |
rs527384016 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233565109 | TTTAAATTACAGGAA[C/T]TAAAAAAGAAATATA | 55230 |
rs527395931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233557408 | CAGAGCACATGTGAA[C/T]AGTCCGAATTATCAA | 55230 |
rs527497176 | snp | C/T | 8.37037e-05 | 0.00646876 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527469 | AGGTCAAATCCCACA[C/T]GCTTTCTGTTTGAGA | 55230 |
rs527513686 | snp | A/C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233549875 | ATTTTCTATAATTAA[A/C/T]ATGCTCCATAATCAT | 55230 |
rs527517776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233489214 | TGCTGGAGTTTATGA[C/T]GAAAAGTGTCACCCA | 55230 |
rs527580735 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233478787 | ACTGGTACATGAAAA[C/T]AGCAAGGTTACCAAG | 55230 |
rs527600087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233479183 | GGGAACTATTGGATG[C/T]CTCCAAATAACAGCC | 55230 |
rs527644604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233549032 | AATGGTAAACAAAAT[C/T]TCCTCAACAAAATAA | 55230 |
rs527670015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233502583 | CTGACCCACACATGT[C/T]TGCACCCAGCCCAAT | 55230 |
rs527671454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233511174 | CTTCTGGCAAAGGTC[A/G]AACCTGATGGTGTTT | 55230 |
rs527692774 | snp | G/T | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486577 | AGCACAGGCCATGGA[G/T]GAAAAGCTATAGATA | 55230 |
rs527735411 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233494757 | CCCAGCCCAGGAGAT[C/T]GAGCTTGCAGTGAGC | 55230 |
rs527756587 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233549599 | TCTTCGTACAATACC[G/T]ATTTACGCTGCTTTA | 55230 |
rs527811101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233488814 | AGGAGGCTGAGGTGG[A/G]AGGATCACTTGAGCC | 55230 |
rs527869917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233526666 | CTTGATCAGAAAGTA[A/G]TGTGGAGCAGGAGGG | 55230 |
rs527882269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233518308 | TCAGTGTCTCATGCC[C/T]GTAATCCCAGCACTT | 55230 |
rs527974426 | snp | C/T | 0.000299805 | 0.0122398 | missense, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233562744 | AAAATACCTTTGCAT[C/T]GGGTTTATCCTTATC | 55230 |
rs527979540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233563191 | AACAAACATCCTTTC[A/G]TGGGAAGGATCCTCT | 55230 |
rs528044161 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233515620 | AAATATGTGTTTCAT[A/T]AATATTTTCTCCCAG | 55230 |
rs528060803 | snp | A/C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233556009 | TAGTCCCAGCTACTC[A/C/G]GGAGGCTAAGGCAGG | 55230 |
rs528085969 | in-del | -/TC | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233510736 | CTACTATGATCTCCA[-/TC]TCTGTCTCGATCACT | 55230 |
rs528116187 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233526174 | GTATTTTCTTAAAAA[G/T]AAACTTCTTATTTAC | 55230 |
rs528214008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486339 | GGCAGCTGGCAGGAG[A/G]AGAGCGGGCTCGAGG | 55230 |
rs528237763 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233492285 | CTAGGTGTGTAGGAG[C/G]CTCTACCATCTAGGT | 55230 |
rs528261132 | snp | A/C | 3.59441e-05 | 0.00423919 | intron-variant | USP40 | GRCh38.p7 | 2:233523142 | AAAATGACTTTTAGA[A/C]ATCCTTTTTCTCTTG | 55230 |
rs528262986 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233514601 | CTAAGTGCAATGGAA[A/T]GCACTAAAGGGCTTT | 55230 |
rs528273505 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233496946 | TTAAATGAATAATAA[A/G]GCAGATATGGAAGAC | 55230 |
rs528362564 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233559000 | CCATTAAAGGCAATA[A/T]AACAGTATTCCTATC | 55230 |
rs528366848 | snp | A/G | | | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485738 | TGCCGGTAAGCCCCA[A/G]TTTCTCTGAGACAGC | 55230 |
rs528418288 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233504645 | TGATATAAAGGGATT[C/T]AATGAGAGGATATAA | 55230 |
rs528422969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233552803 | CAGGATACAAAATCA[A/G]TATTGTGTATTATCT | 55230 |
rs528433948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233559658 | GTCTAAAAATATATA[C/T]TTCTGGCTTGTAATT | 55230 |
rs528571318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233480096 | CTCGAACCCCCACTT[C/T]TGCCATGGTCACGAG | 55230 |
rs528593802 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233480357 | AGACCCAGAGTCCGT[C/G]AGTCGGGGAGTGGGG | 55230 |
rs528594037 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP40 | GRCh38.p7 | 2:233521884 | ATTATGACAATGACC[A/G]TAATATATTAACTAA | 55230 |
rs528660709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233551266 | AACTGAAAATGTCAA[C/T]GGTGCCAAGGTTTAG | 55230 |
rs528723249 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233490098 | TCAACTTAATATGAG[A/G]AAAAAAAAGTATTTT | 55230 |
rs528822047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233537174 | AGGTGTGAGCCACCA[C/T]GTCCAGGCTATGTTA | 55230 |
rs528825620 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233558864 | AAATTTAACATACTT[A/G]TTTAGGGAATGTATT | 55230 |
rs528825867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233551762 | TATCTTTAATGTTGA[C/T]ATCCTGAAATACTAT | 55230 |
rs528833057 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233545282 | GGGAAGAGGCAAACC[A/G]GCAATGTAGAGATGA | 55230 |
rs528867764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233515108 | TTGCTCTTCAGTGAC[A/G]AACAGTATCCATTGC | 55230 |
rs528896317 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | USP40 | GRCh38.p7 | 2:233506978 | AAACAATTCAACAGC[-/A]AAAAAAAAGTACCTG | 55230 |
rs528922169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233507074 | CGCACACAAAAAATG[C/T]TCAACATCACAAATC | 55230 |
rs528947264 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233498879 | TTCATTTTACATTCC[A/G]TCATCTATACCACAA | 55230 |
rs529014013 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233491598 | ACTCATCCCAACCTG[G/T]TCCTCGTGTGTGTGT | 55230 |
rs529021580 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233546152 | ACTGAAGCCACATGA[A/T]GGAATGCCTGCCTGC | 55230 |
rs529042282 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233521192 | TGCATGTGTCACTTA[A/C]TGTGACTAATTAGAG | 55230 |
rs529062424 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233479972 | TCAGGGAGTCTCCTC[C/G]CTCGGCTCCCTGATT | 55230 |
rs529065040 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233521711 | GCCGAAGTCCTCTTT[A/G]GGAATGTACATTAGA | 55230 |
rs529133887 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233522635 | TGACAAAGAGATGCA[A/G]CTTTAAATGTGACCA | 55230 |
rs529150977 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233514498 | CATGGGAAGTGAGTT[G/T]TGAGTACGCAGAAAA | 55230 |
rs529155588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233558379 | ACTAGATTAAAAAAA[A/G]AAAACAAAAAACATG | 55230 |
rs529166811 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233565963 | GAAAACCTGTTGCCA[C/G]AACTAATCCACTGCT | 55230 |
rs529192171 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233566547 | GCCCGAAACCACTGC[C/T]CCGACTCCAGGAGAG | 55230 |
rs529286505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233537122 | CTCCTGGGCTCAAGC[A/G]ATCCTCTTGCCTAGA | 55230 |
rs529296707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233489999 | GGGATCACTTTAAGC[C/T]CCTACTGATATACTT | 55230 |
rs529388849 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233485185 | CTTCACGCTGCCCTC[C/T]TCACATTCCTTGGAT | 55230 |
rs529412204 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233479596 | GAAAACAGTATTTTA[C/G]TGTCTATGTATTAGA | 55230 |
rs529443354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233512214 | TAAATCTAATGGTAA[A/G]AGGTGATACAGAGAT | 55230 |
rs529465921 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | USP40 | GRCh38.p7 | 2:233488835 | CACTTGAGCCCAGGA[G/T]GTTGAGGCTGTAGTT | 55230 |
rs529476545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233556740 | GAAAAAAAAACTCAA[C/T]AAATTACTTTTAGTA | 55230 |
rs529478957 | in-del | -/GTCTATG | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233563096 | TCATGGCTTCCCACT[-/GTCTATG]GCATCAGGTCCCAAA | 55230 |
rs529485862 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233504156 | AAGACATGACAGAAA[A/T]TACACAAATAAGAAA | 55230 |
rs529496880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233505082 | CATGGAAATTAAACA[C/T]GCTTCCAAAGAACCA | 55230 |
rs529556767 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233497526 | GGCTGAGAGGAAACA[C/T]GAAGAATGAAAGATA | 55230 |
rs529587514 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233520485 | TATAAAAAGGTATTT[C/T]CTGAGATGGTGTTTA | 55230 |
rs529591159 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233550509 | CAACAAAAAAAAAAA[A/C]CCCAAAAAGCTCAGC | 55230 |
rs529592976 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233557328 | AGAAAGCAGAGAGGG[A/G]TATACCAGGCACAGA | 55230 |
rs529630736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543855 | CACTGAACTTCCATT[C/T]TGATGCCCATACAGG | 55230 |
rs529641467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233541374 | ATTATCATAAGAAGA[C/T]GAAGTTTGGACAAAG | 55230 |
rs529669167 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, synonymous-codon | USP40 | GRCh38.p7 | 2:233487845 | TAAATCAGTAAGTAC[A/G]GATATGTCAGGTGAT | 55230 |
rs529684566 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233534267 | TGTCTGTTCTAAAAG[A/C]TGGCAGACAAGCTCA | 55230 |
rs529706702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233533069 | ATAAAGGAGAAGATA[C/T]AAAAGAATCAGGAAA | 55230 |
rs529765631 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233525802 | CCTACACAAAGGGCA[C/T]AACAACCATCTAAAC | 55230 |
rs529777008 | snp | A/G | 3.45644e-05 | 0.00415704 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533704 | CAGACTCAGCCTGGA[A/G]AGAACTATTCTTCAA | 55230 |
rs529817426 | in-del | -/GG | 0.00835141 | 0.0640778 | intron-variant | USP40 | GRCh38.p7 | 2:233553064 | GGTTGATGCCATAGA[-/GG]AGCTGAGAAGGAAGG | 55230 |
rs529817751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233477624 | CGTGCATTTGCAATT[A/G]CACAGACAGATCTCA | 55230 |
rs529879762 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233554236 | TCATTATTGTAAAAA[A/T]TTAAAATACAGAAAA | 55230 |
rs529898749 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233501674 | GAATGTGAAGTAAGA[A/C]AGAGAAGAATCAAGG | 55230 |
rs529952103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233493677 | CATTTTTCCTTTTAG[A/G]TTTATTAACTGTCAT | 55230 |
rs529966641 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233487072 | CAAAAGGCACTGTGC[A/C]TATCAAAACCTGACA | 55230 |
rs529987092 | snp | A/G/T | 4.97825e-05 | 0.00498891 | synonymous-codon, missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233540667 | CATGTATTACCTTCC[A/G/T]CAGTGGTCCATGCTG | 55230 |
rs530005897 | snp | A/C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476872 | GGGGCCGGAACGAGT[A/C/G]GGGGAAATGAAGTCC | 55230 |
rs530036438 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233477993 | CCCATGGCACCGTGC[C/G]GCAGGTGCTCTGCGG | 55230 |
rs530067676 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233567640 | TATAAGATTATAGCT[A/G]TATAACCTTATATAA | 55230 |
rs530114797 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477175 | GGCAGCTGGGTGGGC[A/G]ACATCCAGAGCTGCA | 55230 |
rs530180790 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233516671 | CTAGCCTGGGTGACA[C/G]AGCGAGACTCCATCT | 55230 |
rs530186941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233546861 | GAAGGTAGTTTGAGG[A/G]AAGGTATAACAACAC | 55230 |
rs530198982 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233509149 | CCAGGTTGGTCACTC[C/T]TTCCAACCTGTATCA | 55230 |
rs530201244 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233568609 | AAACTAATGGCATGT[C/T]AAAGTATTGTCTGGA | 55230 |
rs530310134 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233541465 | CCATCTGCAAGCCAA[A/G]GAGAGAGGCCTCAGA | 55230 |
rs530320667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233480470 | TGAGCTGAGCAGTGC[A/G]AACTGAGCCTCACGC | 55230 |
rs530331945 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233539363 | ACAACACTCTGAACC[A/G]TAAAACAAGTCCTAA | 55230 |
rs530385978 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233539680 | AAAATTTATAGCTTT[A/T]AAAGTATTAGAAGGT | 55230 |
rs530408857 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486262 | AAGGAAAGAGGTGGC[A/G]GCCTGAGCAGGTACG | 55230 |
rs530445433 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233531846 | AACTTTTGAGCGGAC[A/T]TTGAGAAGTGATCGA | 55230 |
rs530468513 | snp | A/C | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233565642 | ATCCCCCTACCTTAC[A/C]CTTGGGAGTCGATTC | 55230 |
rs530482903 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233547561 | TAACAGGAAGCTATG[A/C]TTTAAGCATTTTACA | 55230 |
rs530499999 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233529300 | TAAAAATTCAGCAGC[C/T]AAACAGACACTTGCA | 55230 |
rs530551059 | snp | C/G | 0.000735786 | 0.0191664 | intron-variant | USP40 | GRCh38.p7 | 2:233540630 | TGAAATTTCTTGGGA[C/G]TAGGACTTCCCAAAA | 55230 |
rs530556774 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233492903 | CATCGTGATGTGTGC[A/G]GCTGAGTGCTGAGTA | 55230 |
rs530624395 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233481634 | ACACGGATCTCTCAT[C/T]GCCGCGCCAGAAGCA | 55230 |
rs530642117 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476607 | CCTGCCCCGCTTCCA[C/T]ACAGGAAGAGAGGCT | 55230 |
rs530671061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233499786 | TTCTCCACACCCTAT[A/G]AATTTTTTTTTCCTA | 55230 |
rs530700297 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233553657 | GCCTCTCATTTCTCC[G/T]CTTATCAAAGTATCT | 55230 |
rs530705059 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | USP40 | GRCh38.p7 | 2:233520436 | TTCAACTTGTTATAG[-/A]AAAAAAACCCATAAT | 55230 |
rs530714550 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233515816 | CAGAAATTTTGTAGT[C/T]TTAGGTTTTAACTTT | 55230 |
rs530741138 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233516613 | GAATGGCGTGAACCC[A/G]GGAAGCAAAGGTTGC | 55230 |
rs530747760 | in-del | -/A | | | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475159 | CCACAAACGTTCCTT[-/A]TTTTATTTATGTATT | 55230 |
rs530819920 | snp | C/T | 1.65638e-05 | 0.00287778 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523242 | TCCCTGAACGTCTTC[C/T]TCATGTCTTCCTTGG | 55230 |
rs530820858 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | USP40 | GRCh38.p7 | 2:233538114 | CATGTTAATTTATAT[A/T]TAGTGTAATCGCTAG | 55230 |
rs530849075 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP40 | GRCh38.p7 | 2:233480424 | GCATGGAGCTGATGC[C/T]ACGGGCAGGTCCTGG | 55230 |
rs530965165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233545455 | TGTCATGGAGCCTTC[C/T]TTGCCCCACTTCCTC | 55230 |
rs530982382 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233538081 | CATAAAGTGGTATAC[C/T]ATTAATTTGTAATTT | 55230 |
rs531044136 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476856 | CAGACGTGGAGCATG[C/T]GGGGCCGGAACGAGT | 55230 |
rs531084911 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233475963 | TGCGAGTCTCCTGAG[C/T]GGGGTTAGTGTTTGG | 55230 |
rs531152984 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233538262 | AAACAAATAGCAAGA[C/T]GAGAGATTCAAACAC | 55230 |
rs531171519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233478663 | TGTGATGGTGACAGA[C/T]TGGCGACAGCCTGGA | 55230 |
rs531183490 | in-del | -/TACA | 0.00835141 | 0.0640778 | intron-variant | USP40 | GRCh38.p7 | 2:233553063 | GGGTTGATGCCATAG[-/TACA]AAGCTGAGAAGGAAG | 55230 |
rs531221066 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233534823 | CGTTTTTCTTTGTTT[C/G]ATAGTTGAGAATTAA | 55230 |
rs531227856 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233491571 | GTTAGCTTCCTGTTT[C/T]CTCATCATAACACTC | 55230 |
rs531279495 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233519658 | ATGGCTTTAATTCGA[A/G]TATCAAACACCATCT | 55230 |
rs531284037 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233479070 | TTGTGCAAACAGCAC[C/G]TGTGAGGCTTAAGAT | 55230 |
rs531311923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233564218 | TTTCTAAGCTTAGAA[A/G]CAACAGAAGAACCAC | 55230 |
rs531347209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233518989 | ACCTCAAAAATGATA[C/T]GCTATGTGAAAGAAG | 55230 |
rs531399275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233511564 | TAAACATCTAGAACT[A/G]TAAGGATATATTCCT | 55230 |
rs531425815 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233563409 | CTGTATCCGAGCCTA[C/G]GTAGGAACTCTTACT | 55230 |
rs531428443 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233542780 | TGAATTCCAGCTCCT[C/G]GTTGAGCAATCCTGG | 55230 |
rs531439679 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233556266 | GGGCAAACAGGATTA[A/C]ATTTACATGAGCAAA | 55230 |
rs531558756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233533965 | AACCACAGTGCTCTG[C/T]TAAATAGTCTGATAG | 55230 |
rs531564363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233555051 | AAAAAAAATTAGCTG[A/G]GTGTGGTGGTGCATG | 55230 |
rs531566858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233495637 | AGCACACTTCAGTGT[A/G]TGCAAGTGTGTGTGT | 55230 |
rs531593519 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233518210 | TGTGCTCAAAATATG[G/T]TTTTTTTTTTAAAAG | 55230 |
rs531616600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233482848 | CATGTGTGTGGGAGT[C/T]CCCACGGTCTCACTA | 55230 |
rs531657791 | snp | G/T | 3.31241e-05 | 0.00406952 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523262 | GTCTTCCTTGGGGAT[G/T]GCCGTCCAACCCTCC | 55230 |
rs531739475 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233516995 | CTTGCACATATTTTG[C/T]TCATTTATGTCTAAG | 55230 |
rs531778863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233501936 | AGCAAACTGAGAAGG[A/G]TAGGCCAGTGGGATA | 55230 |
rs531788231 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233533027 | AAAGGATAAATAATA[G/T]AAATAAAAGATATAA | 55230 |
rs531798279 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233525731 | AGGCATCACTTGTTA[A/C]ATTAGTCAAAGCCAA | 55230 |
rs531809061 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233525019 | ATTAGATGTTACTGC[C/T]GCTACTGTTAATTCT | 55230 |
rs531841396 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233568751 | CACGTCACTATAAGA[C/T]GCACTATCCATCTAA | 55230 |
rs531860002 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP40 | GRCh38.p7 | 2:233494586 | TTAAAAGATTTTTGG[C/T]TGGGCTTGGTGGCTC | 55230 |
rs531888426 | snp | A/C | 8.36785e-05 | 0.00646779 | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233561248 | GAACCAAAAAAGAGC[A/C]CGCATCGCCAAGTCA | 55230 |
rs532019624 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233477581 | ACGAAGACCCCAAAA[A/T]ACACTCCAATTTTAT | 55230 |
rs532062758 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233513316 | TCTTTGTGTACTTTC[C/T]TCTCTGTTGGTCAAT | 55230 |
rs532072796 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233513735 | CCAGCATGTGCTATG[G/T]TTGAGGATACAGATT | 55230 |
rs532079676 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233527353 | AATGAAATGGAGAGT[C/T]TAGCTGGAGATGGTG | 55230 |
rs532119148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233478431 | CATGAGTGAATGGCT[A/G]AGCATATTTTTATAT | 55230 |
rs532141261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233533845 | TAGATGTGATTAAAA[A/G]ATGTTTTCTTCCTTT | 55230 |
rs532147067 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233478337 | TCTGCGTCCTCAACA[C/T]ACGAGTCTTTCCCAC | 55230 |
rs532201901 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233518475 | GGGAGGCTGAGGCAG[A/G]AAAATTGCTTGAGCC | 55230 |
rs532223761 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233501236 | AGAGAGCATAAAAGC[C/T]TTATTTCAGAAACAG | 55230 |
rs532230453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233548815 | TGATAACGTTAATAA[C/T]GTGTGTCTGTGTATG | 55230 |
rs532233400 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233478080 | ACAGAAAGCCTCCGC[A/G]GCCCACCCGCCATCC | 55230 |
rs532239491 | in-del | -/TA | | | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233565941 | ACAGGTTTTCTTTTT[-/TA]AAAAAATTAGTGATG | 55230 |
rs532293750 | snp | A/C | 6.73061e-05 | 0.00580073 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233488281 | TCTAAGCAGATCTCA[A/C]TTCTCCGTCCTAGTT | 55230 |
rs532345375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233560863 | CTTTAAATAGACTTC[C/T]GGGGGAAGCTAATGT | 55230 |
rs532353974 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233541818 | TCAGGTCACATAGAC[A/T]TTAAAAGGATAATAT | 55230 |
rs532367969 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP40 | GRCh38.p7 | 2:233541427 | CAGAAGAAACACCAT[A/G]TGAGGACACAGGAAG | 55230 |
rs532418751 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233508570 | CTGAATTTCTATGTT[A/G]TCTGAGTGTTGCTCT | 55230 |
rs532455634 | snp | A/G | 7.69971e-05 | 0.00620424 | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233561238 | AGTTCATATGGAACC[A/G]AAAAAGAGCCCGCAT | 55230 |
rs532470389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233500877 | GCAAAGGTCTGGAGG[A/G]ACACATACTCTGCTG | 55230 |
rs532533575 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233482510 | CCTTGGTTGTATCGA[C/T]GGGCATCTGTGTACT | 55230 |
rs532567332 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233484038 | TCCATGCTGCACTGT[C/T]GCCACAGCTGTGATC | 55230 |
rs532675682 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233568649 | CATTCCATAGCTTCC[G/T]CTCCTCCTATCAGAT | 55230 |
rs532688538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233554971 | ATACTAAAGAAGTTA[C/T]AAGAAAAAAAAATTA | 55230 |
rs532736968 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233565930 | AGGCACGTTCACATC[A/C]CTAATTTTTTTAAAA | 55230 |
rs532738852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233557478 | ACAACTAAAACAAGA[C/T]TAACACAGTGTTACT | 55230 |
rs532789701 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486944 | GAGGCTGCTGGAGAG[A/C]AACAGGAGGGACTAG | 55230 |
rs532816565 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233514379 | AAGACCAAATAAACA[A/G]CTGAAGTTAAAAGCA | 55230 |
rs532849566 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233481592 | GGGCTACCAGGCAAC[A/G]TGAAGACAGAGATCA | 55230 |
rs532870373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233524614 | CCATCAGAAACAACT[A/G]AGCTAAAGAAAGAGC | 55230 |
rs532914445 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233552224 | AAAAAAAGTTGAATG[-/A]AAAAAAAAAAAACAA | 55230 |
rs532937626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233513476 | AGTCAATGGTTACTG[C/T]TTGTGGTGCACATGT | 55230 |
rs532955633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233537023 | CAAATAGCTGGGATT[A/G]CATGTGCGCACCACC | 55230 |
rs533001883 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233505502 | AATCAGACATTACAA[C/T]TGATACCACAGACAT | 55230 |
rs533065613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233565124 | TTAAAAAAGAAATAT[A/G]TTGCTTTATTTTTTT | 55230 |
rs533086732 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233475531 | AGCTAAGGGCTACAA[C/T]TTTAAAAAATGGTTT | 55230 |
rs533118449 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233546275 | GAGATGTCCAGGAAA[C/T]CACAACCCAAAAGAA | 55230 |
rs533139916 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233504057 | AGACTATTTTTATAT[G/T]ACCAAAGGTGAGTTG | 55230 |
rs533166017 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233498215 | TCAAAACATTCAGGG[A/G]CCAAAACTTCAGAGT | 55230 |
rs533175575 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543780 | TTTACAAATTACCCA[G/T]CCTAAGTGTTGTGAT | 55230 |
rs533196439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233479293 | AACAGAGCCAGGCGC[A/G]GTGGCTCACGCCTGT | 55230 |
rs533198284 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP40 | GRCh38.p7 | 2:233484474 | AGTCTTTTGAATCTC[C/T]TTTTTTTTTTTTTCT | 55230 |
rs533217195 | snp | C/G | 1.66139e-05 | 0.00288213 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233496787 | GTCCTTCAATTAAAA[C/G]CAAAGTATCTCCAGA | 55230 |
rs533217306 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233537308 | ATGTGGGTGTCATCT[-/G]GGGGATTCTAGAACC | 55230 |
rs533244189 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233525181 | AACTATGTTGTTCAA[C/T]AATATGTGTCAATAT | 55230 |
rs533261795 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233479518 | AAGTGGGTTGAGATC[A/G]TGCCACTGCACTCCA | 55230 |
rs533282406 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233535705 | CATAATCTAGACTCT[C/T]CACAACACATCATCC | 55230 |
rs533343158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233495982 | CGAATACATTAAAAA[A/G]GATATGCACATATTT | 55230 |
rs533409998 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233488854 | GAGGCTGTAGTTGAG[A/C]CATGATCACGCCACT | 55230 |
rs533464443 | snp | C/G | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486779 | TCAGGGGAGTGCAGA[C/G]TGCAAGAGCAGAGGC | 55230 |
rs533503589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233556695 | TGGAGAAATCTGGAT[C/T]ATAGGCTCATGATTT | 55230 |
rs533536992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233563314 | GTTGGCAACCCCATG[C/T]GAGTCTCCAGAATTT | 55230 |
rs533618841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233483683 | CTAATCCAGAAATCC[A/G]AAACTCAATGGAGCA | 55230 |
rs533703057 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233546975 | AATTGGGAAGGTGCC[C/T]GGCAAGCTGGTATCT | 55230 |
rs533731232 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | USP40 | GRCh38.p7 | 2:233549654 | CATCCCCTTTTTTTA[C/T]TGATATATATCTAGT | 55230 |
rs533748545 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233514976 | AGATTTTATTTGTCT[A/G]AAGTGTCCTATGTAT | 55230 |
rs533766213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233511624 | TTTTAGAGAAAAACA[A/G]TATTACTGGAGTAGC | 55230 |
rs533779656 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233502794 | AAGAACTGGCATAGG[G/T]ATCATGCTACTGAGC | 55230 |
rs533856679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233549928 | CCACACTAGCAATTA[A/G]AAACAAAATAAAATA | 55230 |
rs533922408 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233550633 | AGCTAGCTAATAAAT[C/G]TTCTATTCTGAATAA | 55230 |
rs533926650 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233512060 | TACTTAATAAAAATG[A/G]CTTGTTCAAAGAGCT | 55230 |
rs534021059 | snp | A/C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233515940 | TGTTGAAAAAATGCT[A/C/G]TCTCTCTGCATGAAA | 55230 |
rs534074183 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233534097 | AGAACAAACACTTTT[C/G]AAATATTTAAAAGCA | 55230 |
rs534093565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562963 | TTACTTTCTTGTAAC[A/G]TTTTTAACCAGTGAC | 55230 |
rs534096037 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233542618 | AGGAGGTCAAGGCTG[C/T]AGTAGGCCGTGATTG | 55230 |
rs534097250 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233558287 | AAAAAACAAAAAAAA[A/T]TTTCACAGCATTAAG | 55230 |
rs534103723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233555944 | ATGGTGAAACCCCGT[C/T]TCTACTAAAAAAATA | 55230 |
rs534111852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233519109 | TTGCCAGGGGCTTGG[A/G]ATACAGATGGGTACA | 55230 |
rs534126921 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233510978 | TCAGCTTGTCATGCA[C/T]TACTATTTGCTACGG | 55230 |
rs534151144 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233554595 | CATCATCAACTCACA[A/T]ATATATTGGGAATAA | 55230 |
rs534155038 | snp | C/G | 0.36021 | 0.224397 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233561328 | AACTATACTACAAGG[C/G]TACAGTAACCAAAAC | 55230 |
rs534210768 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233555207 | CAAAAAAAAGAATTA[C/G]GTTAAGCTAGGATAA | 55230 |
rs534223024 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233548534 | GGTTCCAGATTACAG[A/G]AGAGTTAGCTAACTA | 55230 |
rs534256993 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233482460 | CACACACCTATGGGC[A/G]AGTTATTCTAGGGAA | 55230 |
rs534281001 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233483127 | TATGATTTCCTTTGA[C/T]GAACAAAAGTTCTCA | 55230 |
rs534320317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233477885 | CCTGTGTGACATGAT[A/G]CAGAGGCTGCCTCTG | 55230 |
rs534333262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233526203 | ACAAGTGATTAGTTT[A/G]CTGTGAATTAAGTTT | 55230 |
rs534338750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233539051 | AGGCAAGCATTTCAC[A/G]CCAGGAGGCAATAAC | 55230 |
rs534343894 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233530865 | GTTTTCCATTAGCTT[C/G]TCATTTGCCTTTTAA | 55230 |
rs534383210 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233480202 | GTCCCTGGCACACGG[G/T]CAGCCAAGATACTGA | 55230 |
rs534415513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233501283 | GCTGAAGCACAGTGA[A/G]TAAGAGGGGGAAATG | 55230 |
rs534426746 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233518933 | AGACTAGTCAGCAAT[A/G]CAAAGGAACAAGCTA | 55230 |
rs534442436 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476252 | GCTTCCCATCAGTGA[C/T]GGGGCTGACGAGAAA | 55230 |
rs534469276 | snp | C/T | 0.000129086 | 0.00803284 | intron-variant | USP40 | GRCh38.p7 | 2:233493325 | ATTTTCAAGATCTTA[C/T]GTTTTAAAAATAAAT | 55230 |
rs534511715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233505723 | ACCTAATGGCTTCAC[C/T]GCTGAATTCTACCAA | 55230 |
rs534582955 | snp | A/C/G | 2.25289e-05 | 0.00335618 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233491210 | TCTTCTGAGATCTCT[A/C/G]TGTCTCCCAAGTAGA | 55230 |
rs534648931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233545583 | AGATCTACATTCACA[C/T]TTTGCAGTTAGTGGC | 55230 |
rs534650463 | snp | A/G | 5.72131e-05 | 0.00534821 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485751 | CAATTTCTCTGAGAC[A/G]GCCCCACAACTTTAC | 55230 |
rs534655321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233520558 | AAGAACACCTGGCTT[C/T]ACAGAAAAACAGAGT | 55230 |
rs534715652 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233512967 | TTTTGTTGAAACATT[G/T]AAAACCCTCTTCGTT | 55230 |
rs534758433 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233563819 | ATGTCAAATCATATG[C/T]TTGGCCAGCAATCCC | 55230 |
rs534817302 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233557636 | AGGAAGAGCAGCTGG[C/G]GGGAGGGCCAGGAGA | 55230 |
rs534824497 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233506382 | TTAAATGTAAAACCC[A/C]AAACAATGAAACTAC | 55230 |
rs534870379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233488921 | ATTAAGAAAAGAAAG[A/G]AAAGGAAAGAAAGGA | 55230 |
rs534885834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233490287 | TCCTGCCTCAGCCTC[C/T]GAGTAGCTGGGATTA | 55230 |
rs534890996 | snp | A/G | 7.08291e-05 | 0.00595059 | intron-variant | USP40 | GRCh38.p7 | 2:233498519 | TAAATGTAATCATAC[A/G]AAAGTACAATGTATA | 55230 |
rs534943180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233484204 | TTGGCCCTTTGCTCT[A/G]GTGTACGAATTTATG | 55230 |
rs534987068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233536217 | GAATTTAAAGGAAAA[A/G]ATGAATAGAATGGGT | 55230 |
rs535005489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233558252 | GTCCTAGAGGGTTTT[C/T]TGCAAGATCTTATTT | 55230 |
rs535021451 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233530338 | ATAAATGATTACATA[C/G]TAGTCCATTCTATAA | 55230 |
rs535048850 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233528322 | AACCTCCCGAGACCA[A/C]ATTATCCAGGCTAAA | 55230 |
rs535050015 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233479704 | GCAGCCAGCGCTGCA[G/T]CCCCTCTCCCATATC | 55230 |
rs535051221 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233551086 | GGTCAATCTTGCCCA[C/T]GCTGTCCTCGCAGGA | 55230 |
rs535062904 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233516160 | CCATAGTTTGCTGAC[C/T]TCCTCTCTATATGTC | 55230 |
rs535069260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233545058 | AAATCAAGTTCTTAA[A/G]AAGCAAACAAACAAG | 55230 |
rs535093619 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562482 | ACGAGTGAGAATATG[C/T]GGTGTTTGGTTTTTT | 55230 |
rs535120751 | snp | A/G | 0.000798403 | 0.0199641 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233565432 | CTGATTTCTGATTCC[A/G]CTTAAATTGGTGAAT | 55230 |
rs535157418 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233484900 | TTCATTGCCCGTGTT[C/G]TTTAGTACAGTGTTA | 55230 |
rs535175076 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233495585 | TTAATAAACCTATTA[A/C]AATTCTTCAGTAACA | 55230 |
rs535177425 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233537555 | GATAAAAAGAAAATC[A/T]TAAAAGTAGACCAAG | 55230 |
rs535178069 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233535332 | CAAATTAGAAAGAGA[C/T]AGCAAACTTTTTCTT | 55230 |
rs535195729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543917 | CCAAAGGAGGGAGTC[A/G]AGGGACTGGTCTTTC | 55230 |
rs535202954 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233497072 | AGTTAGATGAGATGA[C/G]AAATGAGAAACTGAT | 55230 |
rs535214533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233479839 | AGTCAGCAAAGGCCA[C/T]GGGACAGTGCTGTCC | 55230 |
rs535272800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233483767 | AATATTCCAAAACCC[A/G]AAAAAACCTGAAATC | 55230 |
rs535341411 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233503951 | AAAATAGCCAAAAAC[-/A]ACAACAGTTACTATT | 55230 |
rs535351020 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233550803 | TCTTTCCCTATGTCT[G/T]AAGGATTACAGATTC | 55230 |
rs535362491 | snp | A/G/T | 3.50504e-05 | 0.00418619 | intron-variant | USP40 | GRCh38.p7 | 2:233551370 | TAAAAATAAAATAGT[A/G/T]CAAACCTGTTCACAA | 55230 |
rs535491058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233490244 | TCTCAGCTCATTGCA[A/G]CCTCCCTGTCCTGGG | 55230 |
rs535544317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233553189 | TTATATTAATGTTAA[C/T]GAATTACTAGTATTT | 55230 |
rs535553456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485686 | AGTTCTCACTAACTT[C/T]TCTATCACTGTGAAA | 55230 |
rs535574123 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233538430 | AATAAACTTGATAAA[A/C]CCCAGCAATGAAAAA | 55230 |
rs535605250 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233549589 | GAGAAACCCATCTTC[A/G]TACAATACCTATTTA | 55230 |
rs535630170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233495171 | GATAGCTTCACAGCA[C/T]ACACTAGGAGATAAA | 55230 |
rs535719275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233497341 | GAGCCACACAAGATT[C/T]CTGAGGAGATTTTCC | 55230 |
rs535720891 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, synonymous-codon | USP40 | GRCh38.p7 | 2:233487803 | CAAGTACTTATATTC[C/T]AGTAGTGGGAGACAG | 55230 |
rs535723562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233534437 | GTCTGGCCTTGAGTC[C/T]CTTTCTTTTCTCTCA | 55230 |
rs535726378 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233488890 | CCAGCCTGGGCGACA[C/G]AGCCAGACCCTGTCT | 55230 |
rs535746211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233544352 | ACCAACCCAGAAATG[C/T]CCCAAACCTAATTTT | 55230 |
rs535749928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543213 | AAAACCAGAAATACA[A/G]ATAGTCCTAAACAAT | 55230 |
rs535790654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233483646 | TTTTATGGGGCCTGA[C/T]GCTGACTCAAGTCAA | 55230 |
rs535793825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233535872 | TAATAACATACTGTA[C/T]ATTTCAAAATTGCTG | 55230 |
rs535799537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233524052 | TACAACTAGCACTGA[C/T]TGTCCCTAACATTTA | 55230 |
rs535808626 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233519863 | AAACTTAGGACTTCA[C/T]AGTTAAGTTTTTACC | 55230 |
rs535810222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233535229 | TGGACAGCTCAAAGA[A/G]CCCAGCAGAGAGTAT | 55230 |
rs535856345 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233519330 | CATTCAGTATAGTAC[A/G]ACATGAATACATGGA | 55230 |
rs535861678 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233525288 | AGAAGAATTTCACAC[A/G]TTATATAAACTGGAT | 55230 |
rs535881476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233481639 | GATCTCTCATCGCCG[C/T]GCCAGAAGCACAGCT | 55230 |
rs535896209 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233563878 | CTCTCAGTACTACTC[C/T]TGCCTAATGGTACGC | 55230 |
rs535902207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233481673 | TACTTTATAGACACC[A/G]TCAGTCTGTTCTCGC | 55230 |
rs535946030 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233494340 | AAATATGGGTAAACT[C/T]GAACATTTGTAAGTT | 55230 |
rs536012256 | in-del | -/AAAACATACCTA | | | intron-variant | USP40 | GRCh38.p7 | 2:233526911 | GTTGCTATCATCATT[-/AAAACATACCTA]GAAAAATGACTTGGA | 55230 |
rs536034668 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233546776 | TATTTGATAAGATAA[C/G]GGGAGTTTAAGGCGG | 55230 |
rs536085116 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233488531 | GTCTGGCTCTGGGAA[C/G]ATGGCCAAACTGCCA | 55230 |
rs536089189 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233490977 | CAGAGGAGGGACCAG[G/T]GAGGCCACGAGGAGC | 55230 |
rs536089455 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233492504 | AATCTATATCCAATT[C/G]TATATGTAACTAGAA | 55230 |
rs536106251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486029 | AACAAACAAAACCAC[A/G]TGGTAACTTGAGGCA | 55230 |
rs536146929 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | USP40 | GRCh38.p7 | 2:233539197 | TAAAAATTCCTCAGT[-/A]ATTAATAGAAAAGGC | 55230 |
rs536199937 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233499223 | GTCCATGTGTTCTCA[C/T]TGTTTGGCTCCCACT | 55230 |
rs536322029 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP40 | GRCh38.p7 | 2:233499167 | CACTCCCACCCCCCC[A/C]TACACCAACAGGCCC | 55230 |
rs536359939 | snp | C/T | 9.81306e-05 | 0.00700398 | intron-variant | USP40 | GRCh38.p7 | 2:233561022 | CCCATAGGGTATAGG[C/T]CAAGTCACTTTCTGG | 55230 |
rs536364996 | in-del | -/A | 0.0107246 | 0.0724382 | intron-variant | USP40 | GRCh38.p7 | 2:233555035 | CTCTACTAAAAATAC[-/A]AAAAAAAATTAGCTG | 55230 |
rs536493387 | in-del | -/C | 0.0123036 | 0.0774623 | intron-variant | USP40 | GRCh38.p7 | 2:233527900 | CTAGAGACCTGCTTA[-/C]ATCATTATGTTAAGT | 55230 |
rs536507909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486590 | GAGGAAAAGCTATAG[A/G]TAAGAACTGGAAGGC | 55230 |
rs536557941 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP40 | GRCh38.p7 | 2:233558653 | TGGAGTTTCTTTTTG[C/G]GGTGGTAAAAATTTT | 55230 |
rs536605296 | in-del | -/A | 0.138207 | 0.223612 | intron-variant | USP40 | GRCh38.p7 | 2:233540124 | AGTGGACCTCAACTC[-/A]AAAAAAAAAAAAAAA | 55230 |
rs536614983 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233490435 | CCTCAGACTCCTAAA[A/C/G]TGCTGGGATTATAGG | 55230 |
rs536670712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233523581 | TCTTAGAGAACAACC[C/T]TCATTTTTTCCAAGT | 55230 |
rs536675571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233559242 | TGAGAGAAAGCCCAC[A/G]TACAACAAGATTCAT | 55230 |
rs536701187 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233566912 | GGGAGCGGGAGCGGG[C/G]AAGGTGAGCTCGCTT | 55230 |
rs536744959 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233553736 | CTACTGATATATGAA[C/T]GTGATGAATAAATTT | 55230 |
rs536745235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233546580 | ACTGAAGAGAGACAC[A/G]GCAATATTGAAAAAG | 55230 |
rs536794991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233530709 | TGATTACAGGTTAAA[C/T]TGAAAATTTTTTGAA | 55230 |
rs536827807 | snp | C/T | 3.38816e-05 | 0.00411578 | stop-gained, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233498603 | ATTTTTCGTAAATGC[C/T]AGGCATCTCCTATAA | 55230 |
rs536851925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233522177 | GGGTAATGGAAAGCA[A/G]GATACAACTACTTAT | 55230 |
rs536880411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233480128 | TCACGCTCACCTGCC[C/T]TGCCACCTCCACCTG | 55230 |
rs536887354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233499073 | CGTGTGCCATGGTGG[C/T]TTGCTGCACCTATCA | 55230 |
rs536899263 | snp | C/T | 0.000128614 | 0.00801813 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485779 | TACCCAGCTAGATAT[C/T]GGAAGCCACTCGAAC | 55230 |
rs536920056 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233502784 | ATTACAGCTGAAGAA[C/G]TGGCATAGGGATCAT | 55230 |
rs536924756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233538590 | AGATAAATGAACAAA[C/T]TCCTTAAAAACCATA | 55230 |
rs537040098 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233514021 | ACATAAATCTCTTGT[C/T]GACGGAAACAATTTA | 55230 |
rs537050740 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233505789 | CAGAAAATTGAAAAG[C/T]TGTGAATATTTCCAA | 55230 |
rs537069495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233480747 | GTAGCAGCCCTGAAG[C/T]CACAGCAGCGTCCCC | 55230 |
rs537097173 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233532283 | TCGTTTGCAAATAAG[A/T]GTAACGTTGTAACTT | 55230 |
rs537132333 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476657 | CAGCTGCAGTCCTCG[A/G]GATCCAAGGACCTTC | 55230 |
rs537132348 | snp | A/G | 0.000654236 | 0.0180746 | intron-variant | USP40 | GRCh38.p7 | 2:233481177 | GGCTCTGTCAGCTGC[A/G]CATCTGTGCAGACCC | 55230 |
rs537135967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233488570 | TCCCTCTGTTCAGCC[A/G]GGGTTAAGATTCTCA | 55230 |
rs537153845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233552280 | GTAGATTTTCAAACA[A/G]GCTCTAAAAATGCAT | 55230 |
rs537214446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233487275 | CACTGGAGAATATGA[A/G]AACAAGATAATCATC | 55230 |
rs537215148 | in-del | -/GGAGCG | 0.00119737 | 0.0244387 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233566891 | AAGAGTTTGGGAACT[-/GGAGCG]GGAGCGGGAGCGGGA | 55230 |
rs537305927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233491904 | TCACTTATTTTTGCC[C/T]TAACTGTCTTTACTG | 55230 |
rs537327419 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233498988 | TCCAGGTGGTATACA[A/T]CTTAGCGTTCTTTTT | 55230 |
rs537339723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233479724 | TCTCCCATATCCCAG[A/G]TCTCTGAGGGCACCA | 55230 |
rs537369705 | snp | A/G | 0.000219386 | 0.0104712 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485993 | CTGTACCAGAAAACC[A/G]TCAAGCGCCAGATCC | 55230 |
rs537378400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233521352 | CACATTTTTCACAGA[A/G]AACTTCTGTAAGTAA | 55230 |
rs537415781 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476120 | GGTTTGGACTGTTGG[A/G]AGGAGTATGAGGGAC | 55230 |
rs537442772 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233518508 | GGAGACGGAGGTTGC[A/T]GTGAGCGGAGATCGT | 55230 |
rs537444487 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233510940 | TTTCTAACTCAACCT[A/C]ACTTGTCATGTTTTC | 55230 |
rs537450086 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233502247 | AATGTAAAGTTAAAA[A/G]GGCCAGTAAAAAACT | 55230 |
rs537451371 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233522100 | ACTATAATGTCACAT[A/C]GATTACTATGTAGCC | 55230 |
rs537472487 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233566179 | GGGAAGGGGAGCGGA[A/G]GGCGGGGAAGACTGC | 55230 |
rs537473254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562897 | TTTAAGTAAAATCAA[A/G]TAGATTCAGAAATAT | 55230 |
rs537605054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233528512 | AGAGCACAACCACAC[A/G]AAAGACCTTAGTGCG | 55230 |
rs537611422 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233475964 | GCGAGTCTCCTGAGC[A/G]GGGTTAGTGTTTGGG | 55230 |
rs537624664 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233501759 | AAAAAGAGAAAAATA[C/T]GAGCGGGTTATGTTT | 55230 |
rs537652874 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233484096 | TGTCCTTTTTCTTCT[C/T]GCAGTGAGCCAAGAT | 55230 |
rs537666094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233529310 | GCAGCCAAACAGACA[C/T]TTGCATTAACAAGTT | 55230 |
rs537680578 | snp | A/C/G | 6.74347e-05 | 0.00580633 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477432 | GAGAGAGAAGTTTCC[A/C/G]GGGCTCGGGGCCGGG | 55230 |
rs537689493 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233507374 | AGATATCTGCACTCC[C/T]ATGTTTAATGGAGCA | 55230 |
rs537870065 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233555436 | TTAACTCATGGTGAA[C/G]ATTTCAAGTACCAAA | 55230 |
rs537933128 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233555917 | CAGGAGATCGAGACC[A/C]TCCTGGCTAACATGG | 55230 |
rs537952203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233549258 | GAACAAAAATATTGA[C/T]ATAGTTTTCATAAAA | 55230 |
rs537996211 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233540187 | CCCAAGCAACACTGA[A/T]GAAAAAAGGTGAGAA | 55230 |
rs538142457 | snp | G/T | 0.00021411 | 0.0103445 | intron-variant | USP40 | GRCh38.p7 | 2:233560999 | TTCTCGGAAGGCAAA[G/T]TCCATTACCCATAGG | 55230 |
rs538146498 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233555910 | ATGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 55230 |
rs538153250 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233561702 | GCAATGGCAACCAAA[A/G]ACAAAATTGACAAAT | 55230 |
rs538161717 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233547392 | CGTTCCAAATACAAC[G/T]GATAGAATGTCAGAA | 55230 |
rs538185426 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | USP40 | GRCh38.p7 | 2:233526505 | TTCAAATCAACTAAG[G/T]TTAAAAGGGAAATTG | 55230 |
rs538206471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233547860 | TATCTGTGAGATTAC[C/T]GACAAGGTGATTCTA | 55230 |
rs538249688 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233525897 | AGGAATTTTTACTCA[A/G]AAGAGCAAGACTAAT | 55230 |
rs538288910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233487321 | TAGGAAATACCTAGA[C/T]GATGAAATAGTCAAT | 55230 |
rs538292604 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233477732 | GCAGCACGGCATGGT[G/T]CAGGCTCTGGGGCTT | 55230 |
rs538310962 | in-del | -/A | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233530250 | CACACACAAACACAC[-/A]CAATTTTAAAAACTG | 55230 |
rs538315213 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233540930 | TTATAAAAAGTTTTT[A/T]AAAAACTGGTTAAGC | 55230 |
rs538321508 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233511258 | ACTATTAGTGCAGAG[A/T]GTAATTAAGTCTAAA | 55230 |
rs538381608 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233532762 | ACCTGGGCAATACAG[C/T]GAGACCCTGTCTCTA | 55230 |
rs538381824 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543842 | CCGATCTTGCTGACA[C/T]TGAACTTCCATTTTG | 55230 |
rs538413360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233532230 | GCCTCTGAATGGGTG[C/T]TGCCTGCAGCCAATC | 55230 |
rs538431644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233516125 | CTTTGCCCACTGGCT[A/G]AAAAAAAACAGGTTG | 55230 |
rs538491819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233487265 | GTCATCAAAGCACTG[A/G]AGAATATGAGAACAA | 55230 |
rs538493625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233481382 | TCTAAAAAACTACCT[A/G]TATTGACAAAAGAAC | 55230 |
rs538504800 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233509187 | GAGCTGGAAAAAAAA[A/T]TTTTTAAGAAAAAAT | 55230 |
rs538507403 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233536102 | TTCATAATCAACAGA[C/T]GGAATGGTCAATTCA | 55230 |
rs538508851 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233481468 | CGATGAAAACAAACT[C/T]GGGGGTGGCAAGAAG | 55230 |
rs538599395 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233506908 | GAGAAAGACTGTCTT[-/A]AAAAAAAAAATCTAA | 55230 |
rs538715435 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233475705 | ACCCACACGCGTCTT[C/T]GGACTTGCAGACATT | 55230 |
rs538733391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233503078 | AATTCAAAACAATGA[C/T]CTTAAGGAAACTCAT | 55230 |
rs538733909 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233561379 | ACAGAGATATAGATC[A/G]ATGCAACAGAACAGA | 55230 |
rs538826651 | in-del | -/AGAA | 0.00795532 | 0.062565 | intron-variant | USP40 | GRCh38.p7 | 2:233488958 | GAAAAGAAAGAAACG[-/AGAA]AGAAAGAAACAAAAA | 55230 |
rs538847195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233532639 | TCTAATTCTTTGTTC[A/G]AAATGCCAAGAACCT | 55230 |
rs538923189 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233480588 | CTTCCTCCAGTGGCA[C/G]TAAGTGCAGAGCCAG | 55230 |
rs538958695 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233525374 | CTACTTAGTTAAGAA[A/C]GTAGTAGGTGGGGAA | 55230 |
rs538971428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233553171 | TATCTATAATAATCA[C/T]TTTTATATTAATGTT | 55230 |
rs539030582 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233500022 | GTCTGACTATATTTA[A/C]TGATTCTTGAATAGG | 55230 |
rs539110151 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233539492 | ACCCCCTAAATATTT[G/T]GAAATTGACCAACAC | 55230 |
rs539123113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233547315 | CTGGTAAACATGTTC[C/T]TGGTAGAACACAGTT | 55230 |
rs539145017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233544200 | CTCAGGAACTTATAC[C/T]ACACTTTATTACAAA | 55230 |
rs539160639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233484278 | ATTTCACTGAATTTA[C/T]AGACTTGGGAAGAAC | 55230 |
rs539230965 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233517717 | ATAGCAGCACAGTTT[C/G]CAATTGCAAAATCAT | 55230 |
rs539241929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233515457 | GGTTTTAATTTGATT[A/G]CTAATGATTCTGAGC | 55230 |
rs539344130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233556405 | ATAAACATAAGCACA[C/T]ATATATAAATGAACT | 55230 |
rs539371361 | snp | A/G | 0 | 0 | intron-variant | USP40 | GRCh38.p7 | 2:233515983 | CTTTGTTGAAAGTCA[A/G]TGACTACGCACCTAT | 55230 |
rs539400143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233496293 | AAGGGCAGTGAAATG[A/G]GCCCTCTCATATGCT | 55230 |
rs539418802 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233504605 | GTTATATAATCACTA[C/T]ATATCATTATTATGT | 55230 |
rs539467870 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233547227 | TAAAATCAACATACT[A/G]AAGAAAGTTACATTT | 55230 |
rs539468562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233535093 | ATTTCAAGAAAAGGC[A/G]AGAGTCTTACTGGGA | 55230 |
rs539536366 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP40 | GRCh38.p7 | 2:233490186 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCACTCTGT | 55230 |
rs539687390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233502726 | CTGTCACAAACACCC[A/G]TAACCTAGGAAATTG | 55230 |
rs539698867 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | USP40 | GRCh38.p7 | 2:233494941 | ATATATATATATATA[C/T]ATATATATATATATT | 55230 |
rs539711476 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233512514 | GGAGGCCACTATTTA[A/T]CAAGAAAGACAGACG | 55230 |
rs539711558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233503735 | AGCTAAAGGAATTTA[C/T]CACCACTAGACCAAT | 55230 |
rs539730600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233541860 | AAATTGCAAAACAGC[A/G]TTTAGTAAAGCTCAA | 55230 |
rs539839615 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | USP40 | GRCh38.p7 | 2:233494401 | TCTGTAGAATAATTT[C/G]CCTGTACCTGTCATA | 55230 |
rs539845193 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233527078 | GTTTTACACAACATG[A/C]TCATCTTTATCTTTT | 55230 |
rs539848148 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233495286 | GTGTGGATATATATG[C/T]TATGTATATACACAT | 55230 |
rs539850180 | snp | C/G | 3.56208e-05 | 0.00422009 | intron-variant | USP40 | GRCh38.p7 | 2:233488226 | ACTTCAGATGCACAG[C/G]AGAATTTCTTACCCC | 55230 |
rs539912293 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233478286 | GTGTCTGTGCCAATT[C/T]CACACCCACACACAG | 55230 |
rs539935128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233517667 | GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCCC | 55230 |
rs539958117 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233518685 | AGTCACTTTGGATAA[C/T]AGTGCGAGAGTTTCT | 55230 |
rs539971456 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | USP40 | GRCh38.p7 | 2:233492192 | CCTGCCACTGTGTTA[C/T]GATTCGCCTTCAGTA | 55230 |
rs540065225 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233556313 | TCCAATTAGATTAAA[C/T]GGGCAATATGTGTCA | 55230 |
rs540066024 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233494037 | TTCTTCCCACCTCAT[C/T]TTTTGTTAGTGAAGA | 55230 |
rs540089433 | snp | A/C | 0.0912534 | 0.193131 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562349 | GACTGGATTAAGAAA[A/C]TGTGGCACATATACA | 55230 |
rs540092345 | snp | A/G | 0.000235211 | 0.0108421 | intron-variant, synonymous-codon | USP40 | GRCh38.p7 | 2:233488016 | ATGCACCTGGTGATT[A/G]CTGAAAAATTAATTC | 55230 |
rs540190312 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233502384 | TGGATTTAAAAAAAA[A/T]TTTTGGAATATCTGC | 55230 |
rs540204678 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233542109 | CCCCACAAACATCAT[G/T]AAAATATAGATACAG | 55230 |
rs540258891 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233503774 | AAAATACTTAAGGGA[G/T]CACTACAACTGGAAA | 55230 |
rs540312966 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233481901 | TCCACAGGGAGGACG[A/C]CTCAGGGGCGCACCC | 55230 |
rs540313674 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233542646 | TTGCGCCACTGCACT[C/G]CAGCATGGATGACAC | 55230 |
rs540375047 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233479763 | GGGCTGCAGAGCTGC[A/G]AATGGGGGTGAGGCC | 55230 |
rs540384033 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233518004 | GGCACAAGAATGATA[A/T]AGTGGACTTTGGGGA | 55230 |
rs540399015 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233547483 | TACTGCTGGCACCAC[A/G]AGATGCCGTATTACA | 55230 |
rs540415381 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233514003 | GGCTAGCATACAATT[C/T]TCACATAAATCTCTT | 55230 |
rs540431543 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233531662 | AGCATAGTTATGTAA[C/T]TGTTTTAGATCTGGA | 55230 |
rs540442291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233501738 | AAATGGAGTTGCCAT[C/T]AACTGAAAAAGAGAA | 55230 |
rs540464437 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | USP40 | GRCh38.p7 | 2:233517390 | ATGGTTTTTTGTTTT[-/G]TTTTTTTTTTTTGAG | 55230 |
rs540489723 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233511560 | TATTTAAACATCTAG[A/T]ACTATAAGGATATAT | 55230 |
rs540547971 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233507861 | CACCACCAAGAAATG[C/T]TAAGTGCATGAGGTA | 55230 |
rs540573552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233541031 | GTAGCTCAAGGTTTC[A/G]TAAATTCCCAACATT | 55230 |
rs540609188 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233481566 | GAGTGGCCAAACAGG[A/G]GGACTTTAAAGGGCT | 55230 |
rs540619042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233487554 | TTGAAAGATAACTTT[C/T]TCATATAACAAGCAG | 55230 |
rs540655034 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233479481 | GGCAGGAGAATCGCT[C/T]GAACCCGGGAGGCGG | 55230 |
rs540670785 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477199 | AGCTGCACCAGCCCC[C/T]GTGGCTGCCACGTGT | 55230 |
rs540745107 | snp | C/G | 0.000800373 | 0.0199886 | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233561206 | AAACCAAGCTCTTCT[C/G]GGCCAAGAGAAAATA | 55230 |
rs540773373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233517320 | CAGCAATCCCACTAC[C/T]GGGTATCTACCCAGA | 55230 |
rs540788505 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233558223 | AGAGACCTTCTCCTA[C/T]CACTGCAGGTCCAGT | 55230 |
rs540836741 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233492790 | AACATAGCTAAAGAG[G/T]TGGGCCTATTAAAAA | 55230 |
rs540897992 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486883 | AGTGCGGCCAGAGGA[A/C]AGAAAGGGCATCGGC | 55230 |
rs541012660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233484978 | TGAAAATGGAAGCTT[C/T]TGAAGCTGGCACAGT | 55230 |
rs541013460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233528863 | CAAATAAAGAAGCAG[C/T]TCAGAGTCAAAGGTG | 55230 |
rs541020249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233511970 | GTTTGATTTTCAATT[C/T]CCATACTCTTAAGAT | 55230 |
rs541068335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233479907 | GGCCCTGGCCCAGGG[A/G]CCGTGCTGCTTGCGG | 55230 |
rs541072703 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233503899 | CGCAATGGTGCTATA[C/T]AAATTTATCAATCCT | 55230 |
rs541099398 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233556593 | CCACAGTCTTCTATT[A/T]GTAAATATCCCCCAA | 55230 |
rs541122169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233550319 | ATAAGTGCTCAATTT[C/T]TTCAATTATTTCAGT | 55230 |
rs541159870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233514223 | TGTCTAATGGGGGAG[A/G]TGGATATTAAAAACA | 55230 |
rs541216488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233497386 | GCAATATGCATGACA[C/T]TGAAGCAGGGAACGC | 55230 |
rs541223874 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233527249 | TCTCTAAAAGACTTA[A/G]GAGAGAAGATTTGGG | 55230 |
rs541237217 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233489848 | GTACAACAAGGGACA[A/C]AACAGCAGCCTTCTT | 55230 |
rs541246116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233518876 | CAATTCATGTTTGTC[C/T]AGGATAAACAAAATG | 55230 |
rs541258800 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233552898 | CATAATGAAGTGACC[A/G]CATAAATATGTCTCT | 55230 |
rs541289976 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233488903 | CAGAGCCAGACCCTG[C/T]CTATTAAGAAAAGAA | 55230 |
rs541313376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233478393 | CACTGTCTCGGAGTA[A/G]CTTGAATTTACACCT | 55230 |
rs541351303 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233524166 | ATGGAGTCTTGCCCT[A/G]TCACCCAGGCTGGAG | 55230 |
rs541381119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233563902 | GGTACGCTCCATGAC[C/T]CGCCCTACACTTCAC | 55230 |
rs541399747 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233524631 | GCTAAAGAAAGAGCT[A/G]AGACAAATATTTGTT | 55230 |
rs541441655 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233527675 | TTACAATAAAGTTCT[C/T]CATCCCACCAAAGTA | 55230 |
rs541444299 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233483882 | TATGATTTTCCTACA[C/T]AGATAACTAATTTTC | 55230 |
rs541471691 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233479163 | AATGGAGCTCCCAGG[C/G]CCTGGGGAACTATTG | 55230 |
rs541585199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233564905 | TGTGAGCTTTCCAGA[C/T]TTCAGAAATGCGTAT | 55230 |
rs541601477 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233566155 | AGTCAGTTCACTGGG[A/G]AGGGAGGGGGGAAGG | 55230 |
rs541632124 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233527892 | ACAAAATGCTAGAGA[A/C]CTGCTTACATCATTA | 55230 |
rs541649487 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233550174 | ATTTGCTTAAAATAT[A/T]AAACTTTTTAAGTGG | 55230 |
rs541670441 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233563311 | GAAGTTGGCAACCCC[A/C]TGCGAGTCTCCAGAA | 55230 |
rs541672583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233479026 | AAGTGGTTACATCAC[A/G]GTGTTCAGAAGACAC | 55230 |
rs541750522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543551 | GTGGGGTCTTCAGGA[A/G]ATAATTAGGTCACAA | 55230 |
rs541762297 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233508645 | ATTTATTAGGAGTTG[-/A]AAAAAATGTAAAATT | 55230 |
rs541763637 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233481903 | CACAGGGAGGACGCC[C/T]CAGGGGCGCACCCAG | 55230 |
rs541776161 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233536811 | AAACAACAGTATAAT[A/C]GTGAAAAATAATAAA | 55230 |
rs541786355 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233535133 | AGAATCTGAGAATAC[A/C]AGAGAGGCGAGATCC | 55230 |
rs541858968 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233502444 | CCAAAAATCTAAATA[C/T]GAAATGCTCCAATGA | 55230 |
rs541873626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233556033 | AGGCAGGAGAATGGC[A/G]TGAACCCGGGAGGTG | 55230 |
rs541925753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233528680 | TTGGTATCTTGGTTT[C/T]TGTTGTTTCTTTGCT | 55230 |
rs541925794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233519706 | TAATGACTAAGTTGT[A/G]AAAAATGGGAGGAGA | 55230 |
rs541934882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233549584 | AGCAAGAGAAACCCA[C/T]CTTCGTACAATACCT | 55230 |
rs541982120 | snp | C/T | 0.00117988 | 0.02426 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533666 | AAGCATCTTGAAAAT[C/T]TGCTGGTCATTCCTT | 55230 |
rs541987017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233520910 | TGAGACAACTGTTCT[A/G]AAAGATTAAGGTATT | 55230 |
rs542046169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233495776 | TGGCCCAGCTTTTCA[C/T]AACACCTGGAATTTT | 55230 |
rs542056270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233496461 | ATGAGGATATAGATC[A/G]ATTAAATTAGTAAAA | 55230 |
rs542166558 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233510729 | ATTTCTTCTACTATG[A/C]TCTCCATCTCTGTCT | 55230 |
rs542182905 | snp | C/T | 0.000115547 | 0.0076 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562721 | AAAGTATAATAATAA[C/T]AATAATAAAAATACC | 55230 |
rs542215112 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233507117 | TAAATCAAAACCACA[A/G]TGAAGTACCATCTCA | 55230 |
rs542227759 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233552064 | AGCTGCTTTTTAAGA[C/G]TATCAGCTGTGCCCA | 55230 |
rs542272801 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233519441 | GGACTTTAACTTCAT[C/T]TATAATGTTTCAAAC | 55230 |
rs542324451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233553971 | TTGGATTTGCCAGAG[C/T]GAGGAAGAACATATG | 55230 |
rs542364651 | in-del | -/T | 0.264935 | 0.269274 | intron-variant | USP40 | GRCh38.p7 | 2:233549645 | TTAAAATGCATCCCC[-/T]TTTTTTTATTGATAT | 55230 |
rs542403998 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233528117 | CTGAGTAGCTGGGAT[C/T]ACATGTGTGTGCCAC | 55230 |
rs542473500 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233504096 | TTAAAATAGTCTATT[A/G]TAAGTACAAGACTCT | 55230 |
rs542494038 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233523066 | TGTCTAGAAATAAAG[A/C]AACATTCAACTCTTG | 55230 |
rs542515437 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233480798 | GAACCTTGGAGAGAG[C/T]GGGAGAAGGACAGGG | 55230 |
rs542517424 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233566578 | CGCCGCGTCCTCAGG[C/T]AGGCCTGGGCAGCCT | 55230 |
rs542526906 | snp | C/T | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486276 | CGGCCTGAGCAGGTA[C/T]GATGTGGCAGAGAGG | 55230 |
rs542547627 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475456 | GGCGTGAGCCACCGC[A/G]CCCGGCCAAAAGTTC | 55230 |
rs542549835 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | USP40 | GRCh38.p7 | 2:233518220 | ATATGTTTTTTTTTT[A/T]AAAAGTCAAAACCAA | 55230 |
rs542597829 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233515167 | TCGCCTGCTCATGGG[C/T]TTTAGGATTGCTTCC | 55230 |
rs542625008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233490616 | AGTCCAACAGTAGGC[A/G]GATGCTGCTTCAACA | 55230 |
rs542627936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233507651 | GTTGACATCGTAGAA[A/G]CAGAGAGTAAAACAG | 55230 |
rs542792250 | in-del | -/TTATA | 0.0103295 | 0.0711199 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233567038 | TATAGCTATATGATC[-/TTATA]TAAGATTATAGCTAT | 55230 |
rs542793420 | snp | A/C/G | 9.12624e-05 | 0.00675454 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485800 | CCACTCGAACTTTTC[A/C/G]GGAAAGTATTTGGCA | 55230 |
rs542834358 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233492082 | TAATCACCTGCTACA[C/T]AATGATTTGGTCAAA | 55230 |
rs542852497 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233480354 | GAGAGACCCAGAGTC[C/T]GTGAGTCGGGGAGTG | 55230 |
rs542932313 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233566950 | CGCTGGTGAGTTCGC[A/G]GGTCCACTCGGCCAG | 55230 |
rs542946269 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233497532 | GAGGAAACATGAAGA[A/C]TGAAAGATAAGGAGG | 55230 |
rs542964250 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476715 | GACCCTTGGCCTGCG[A/G]GCTGACGTGCAGCGG | 55230 |
rs543002174 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233514356 | AAAGGAGAAGGAACA[G/T]CTCATATAAGACCAA | 55230 |
rs543051047 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476362 | GGGAAAGTCAACCGT[C/T]TATGTCCCAAATCAA | 55230 |
rs543068689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233558840 | CGCCAAATACCAGCC[C/T]TACACCAGAAATTTA | 55230 |
rs543102247 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233525249 | TAGCCTTAATTTCAG[-/A]AAAAAATAAAATGTT | 55230 |
rs543112209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233538638 | AGATCCAACTTCATA[C/T]TGAGACACACATGTA | 55230 |
rs543130097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233559496 | GGTAGGTAATCTCCA[C/T]GTAATCGGTGTTGTA | 55230 |
rs543132072 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233552733 | AAATTCAATCTTCCC[A/G]TGAAAGCTACAGGCA | 55230 |
rs543179188 | snp | A/G | 0 | 0 | intron-variant | USP40 | GRCh38.p7 | 2:233537936 | TTAAAAGTCACTAAA[A/G]TGTTTAAGCAGAAGT | 55230 |
rs543195923 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233521447 | CAGGAGCCTACCCCA[C/T]TGGATCTAGATTTCA | 55230 |
rs543221556 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | USP40 | GRCh38.p7 | 2:233514133 | ACTGTGTATTGGCTA[A/C]GTGCCAGGCACTGTG | 55230 |
rs543244015 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233565711 | CAGTAGTTGGGTTTT[A/G]GAGGCAGCAAGATCT | 55230 |
rs543255026 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233559191 | TGTGTAGTGTTCGTA[C/T]ACAGTAGAATGCCTT | 55230 |
rs543279879 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233557395 | ACCTCACTGAGATCA[C/G]AGCACATGTGAATAG | 55230 |
rs543341207 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233551235 | TGAGACAGTCTCCCA[A/C]AACAAAGAATAGTTT | 55230 |
rs543357129 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233551615 | AACAACCTATGACAC[A/C]GTTCTAAGAGAAATA | 55230 |
rs543367701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233522656 | AATGTGACCACAGGA[C/T]TCATGGGGGTAATTC | 55230 |
rs543368394 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476037 | AGTGCTTCACGGAAA[C/G]GCACAGACGTCTATG | 55230 |
rs543401582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233504962 | TACATTAGACCACAA[A/G]ACAAGTCTTAATACA | 55230 |
rs543430914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233515091 | GTGGAACTAGCAGTG[C/T]CTTGCTCTTCAGTGA | 55230 |
rs543447183 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233566461 | ATTCCTGAATTCCCA[A/G]CTCCTACGGCCGGCC | 55230 |
rs543452214 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233497466 | TGGACCTGGAGCCAA[C/G]CATGGGAATGGTCAG | 55230 |
rs543469274 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476262 | AGTGACGGGGCTGAC[A/G]AGAAACCGTGAGGCC | 55230 |
rs543474961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233497879 | CTCCCTAAATCAACC[C/T]TCTGCTGGCATTCAG | 55230 |
rs543480333 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233551045 | AATTCAAAATGACTC[G/T]AAATAAATCAGTGGT | 55230 |
rs543503370 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233532420 | AATCAGACTGATGGC[A/G]GGCTCCCAATTCATT | 55230 |
rs543515078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233489904 | TGTCTGCTCTGCCGA[C/T]GAATCAGCTTTTGAT | 55230 |
rs543564667 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233530044 | GCCTCAAGTGATCTG[C/T]CCGCCTCAGCCTCCC | 55230 |
rs543568428 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233507031 | TTAGTAAACATTTCT[C/G]AAAAGACATACAAAT | 55230 |
rs543621810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233512190 | AATTAGGCTCATCCA[C/T]GACTAAATTAAATCT | 55230 |
rs543622995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233484528 | GTTGCCTGGGCTGCA[A/G]TGCAGTGGCACGATC | 55230 |
rs543629076 | in-del | -/TAAA | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233500443 | ATATTAACAAAAGTT[-/TAAA]TAAAACAAAAATAGT | 55230 |
rs543634580 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233525663 | TGAAGATGACACAGA[A/G]AGCAAGCAAATGAAT | 55230 |
rs543731290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233504080 | GTGAGTTGGATACAG[C/T]TTAAAATAGTCTATT | 55230 |
rs543758382 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233480243 | AAGGGGATTAGGGTG[A/G]GCGGGGCCAGATCAG | 55230 |
rs543868028 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP40 | GRCh38.p7 | 2:233494283 | TTCCATTTTTTTTTT[C/T]CACCTAGCAGACTGT | 55230 |
rs543889523 | snp | A/T | 0.000731481 | 0.0191103 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551442 | AGTTTCCTTGTAGCG[A/T]TCGCATTTCACAAAA | 55230 |
rs543908619 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233533043 | AAATAAAAGATATAA[A/G]TAAGCAGAAAATAAA | 55230 |
rs543972271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233542023 | TTATACTTTTTATCT[C/T]TTGTATATATTTTCT | 55230 |
rs544070762 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233564018 | CCCTATTAGAAATGT[A/T]CTTATTAGTGCTGGC | 55230 |
rs544083285 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233564771 | ATTAATCAAGCAGAT[G/T]AATATTCCTGTAATG | 55230 |
rs544084664 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475292 | CTCAGCCTCCCGAGT[A/G]GCTGGGACTACAGGC | 55230 |
rs544147281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233557251 | GTACATGTAACTCAA[C/T]TCCTTTGACACCCAG | 55230 |
rs544198335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233500293 | CTATAAAAGGCGAGA[C/T]TGATAGCATTTGGGG | 55230 |
rs544211505 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233479362 | AAGGTCAAGAGATTG[A/T]GACCATCCTGGCCAA | 55230 |
rs544220134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233548171 | TCAAGTGGAAAAAAA[C/T]CCTTCTTACACCTCT | 55230 |
rs544241481 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP40 | GRCh38.p7 | 2:233480911 | AGCCAGGCAGAGGGT[A/G]AGGCTGCGGGTGAGG | 55230 |
rs544244746 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233540133 | CAACTCAAAAAAAAA[A/C]AAAAAACAAAAAACA | 55230 |
rs544253571 | snp | A/C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476862 | TGGAGCATGCGGGGC[A/C/T]GGAACGAGTGGGGGA | 55230 |
rs544254014 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233481447 | ATTAAAAAAAATCCT[C/T]TTGCTCGATGAAAAC | 55230 |
rs544255878 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233533966 | CCACAGTGCTCTGTT[-/A]AAATAGTCTGATAGT | 55230 |
rs544288123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233541194 | GGGGGTGAGATGTAG[C/T]GGTGACAGACTGAAT | 55230 |
rs544317791 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477098 | CGTTGTGCATTTTCT[G/T]GTTAAAAGAAAAAAA | 55230 |
rs544318844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486796 | GCAAGAGCAGAGGCT[A/G]CACAGCCCCATGTCC | 55230 |
rs544432846 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543789 | TACCCAGCCTAAGTG[C/T]TGTGATAGAGCAGCC | 55230 |
rs544458748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233560757 | ATTAACTCATTACTC[A/G]ATTTATTTCCAGAGT | 55230 |
rs544470808 | snp | C/T | 6.82384e-05 | 0.00584077 | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233561162 | ATAGATGTAATACCT[C/T]TGCATCGGGTTTATC | 55230 |
rs544482017 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233491580 | CTGTTTCCTCATCAT[A/T]ACACTCATCCCAACC | 55230 |
rs544490360 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476413 | CTATTATTTCTCACA[A/C]ATGCCAATTAAATCC | 55230 |
rs544509016 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233508275 | TTAAATTATTACTTA[A/G]GTTCCTTTGGCTTGA | 55230 |
rs544510676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233546140 | GGCAGTGCAGAGACT[A/G]AAGCCACATGAAGGA | 55230 |
rs544527509 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233515175 | TCATGGGCTTTAGGA[C/T]TGCTTCCAGTTTGGG | 55230 |
rs544581212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233531703 | CCTTTGATTCACATG[C/T]AAATTAGTAACTGCT | 55230 |
rs544596001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233508654 | GGAGTTGAAAAAATG[C/T]AAAATTCTAAAATGC | 55230 |
rs544717391 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233565160 | ACATTATTGTCATCA[A/C]CCAGGATATATTTAA | 55230 |
rs544722718 | in-del | -/TTT | 0.0107246 | 0.0724382 | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475379 | TGTCAGCCAGGCTGG[-/TTT]TTTTACACTCCTGAC | 55230 |
rs544743876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233501364 | TAGGCCCTTGTGCAG[A/G]CATTCAAGACTTCAC | 55230 |
rs544744180 | in-del | -/TG | 0.00318978 | 0.0398085 | intron-variant | USP40 | GRCh38.p7 | 2:233555365 | ATTTATAGTTCTGTA[-/TG]TGTGTGCAACAGCTT | 55230 |
rs544755233 | snp | A/T | 0.000270068 | 0.0116173 | intron-variant | USP40 | GRCh38.p7 | 2:233524444 | CATTACGATGACTTT[A/T]AAAACATCCAAAATT | 55230 |
rs544764777 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233496984 | ATAAGCTAAGACTAT[A/G]AAATCAGTACAGCAT | 55230 |
rs544767209 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233510402 | TCTTTCTTTTTTTTT[A/T]TTTTTTTTTTTTTTT | 55230 |
rs544808390 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233507608 | ATGACCTCACTCATA[G/T]GTGGAATCTTAAAAA | 55230 |
rs544853664 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233500029 | TATATTTAATGATTC[C/T]TGAATAGGCAAGGAT | 55230 |
rs544856108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233492148 | TACTGTATTTTCACT[A/G]TACCTTTTTCTGTTT | 55230 |
rs544873763 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233541350 | AGGCCCTAAGTAAAT[C/T]TGATTGGCATTATCA | 55230 |
rs544895691 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233524223 | CAACCTCCACTTTCC[A/G]GGTTCAAGCGATTCG | 55230 |
rs545056610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233492894 | ACTTCTGCCCATCGT[A/G]ATGTGTGCGGCTGAG | 55230 |
rs545083947 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP40 | GRCh38.p7 | 2:233547521 | GTGGAGCAAGTATTC[A/G]TCAACAACAGCATTA | 55230 |
rs545113703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233480830 | GCCCGCAGCAGGGCT[A/G]AGGTGGCAGCAAGAC | 55230 |
rs545114706 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233492039 | TACCGGAAAGATAAT[A/T]TTAGGAAATTCTAAA | 55230 |
rs545149832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233523793 | GAAGTGCTCCTGGCC[A/G]CCTTCTAGAGATAGA | 55230 |
rs545215374 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476773 | CCTCGGAGGCCACCC[C/T]GTGTGGCTCCTCCTC | 55230 |
rs545263932 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233506128 | GTAACCAAAACAGCA[A/G]GGTACTGGCAAAAAG | 55230 |
rs545267675 | snp | G/T | 0.0588605 | 0.161139 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233567283 | TGATCTTATATAAGA[G/T]TATAGCTATATGATC | 55230 |
rs545289083 | snp | A/C | | | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233568666 | TCCTCCTATCAGATC[A/C]CCATGAAATCTCACC | 55230 |
rs545341837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233560706 | GAACATGATTAGATA[C/T]GCACTTTAAATATCA | 55230 |
rs545442599 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233483825 | GAATCATAGATACTC[A/T]ACTTGTATAAAATTA | 55230 |
rs545462033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233488713 | GAGGCTAGGAGTTCG[C/T]GACCAGACTGGGCAA | 55230 |
rs545506711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233479057 | CAGTGGTCTACTGTT[A/G]TGCAAACAGCACGTG | 55230 |
rs545528581 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233512702 | CAAAATAAAAGGAAG[C/G]TGGTTACAGCATCAA | 55230 |
rs545532463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233531654 | TCATTAACAGCATAG[C/T]TATGTAACTGTTTTA | 55230 |
rs545535270 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233515254 | CAGTAAATACCTAGA[C/T]GTAGAATTGGTAAGT | 55230 |
rs545628986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233527908 | CTGCTTACATCATTA[C/T]GTTAAGTAGCAGATT | 55230 |
rs545677466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233552590 | GTAGGTATCTTTCCA[A/G]CACTGTTCCAAACTC | 55230 |
rs545708730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233555979 | AAATTAGCCAGGCAT[A/G]GTGGCGGGCACCTGT | 55230 |
rs545723697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233545899 | CAGTGTCCACCAGAT[A/G]TATCTACTGCAGGTG | 55230 |
rs545744874 | in-del | -/ATTTTGG | | | intron-variant | USP40 | GRCh38.p7 | 2:233507999 | TTCAGATTTTGGAGC[-/ATTTTGG]ATTTTGGATTTTGGG | 55230 |
rs545747371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233495509 | CGATTTGCCTGCATT[A/G]GCCTCCTAAAGTACT | 55230 |
rs545781473 | snp | C/T | | | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233529574 | GGTTGCTGGAAGAGG[C/T]AGCATGAAGACTAGG | 55230 |
rs545789166 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543488 | GTAGTTAGGTTCCCC[A/C]AAAATTCATACGTTG | 55230 |
rs545796570 | in-del | -/TTTTTTTTTTT | 0.0670745 | 0.170406 | intron-variant | USP40 | GRCh38.p7 | 2:233490161 | CTTTTTCTTTTCTCC[-/TTTTTTTTTTT]TTTTTTTTTTGAGAC | 55230 |
rs545804995 | in-del | -/AATA | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233487716 | GGTGTATCTTTATTT[-/AATA]AATAATTATTGACTA | 55230 |
rs545826781 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233488984 | AACAAAAAGCCTCAA[C/G]GCTGCTTTTTGCAAA | 55230 |
rs545848455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562500 | TATTCTCACTCGTAG[A/G]TGGGAATTGAACAAT | 55230 |
rs545864268 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233479840 | GTCAGCAAAGGCCAC[A/G]GGACAGTGCTGTCCG | 55230 |
rs545874667 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233564900 | GAGGGTGTGAGCTTT[C/T]CAGATTTCAGAAATG | 55230 |
rs545900822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233518076 | ACAAATAGGGTGTAG[C/T]GTATACTGCTCGTGT | 55230 |
rs545904967 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233477976 | CGCTGTGACCCCCCC[A/G]GCCCATGGCACCGTG | 55230 |
rs545906294 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233540895 | CAAACACGTAAGTTG[A/T]TTCCATCATAATTAT | 55230 |
rs545961335 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233541112 | TTTTGGAAGAGATAC[G/T]TAAGTACAAAAACAA | 55230 |
rs545979477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233494505 | CATAGAAAGCCACAT[A/G]TGCAAGAATATTCTT | 55230 |
rs546007924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233548834 | TGTCTGTGTATGCAC[A/G]TGCACAAATGTGGCA | 55230 |
rs546009676 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233502451 | TCTAAATATGAAATG[C/T]TCCAATGAATATTTT | 55230 |
rs546061984 | snp | C/T | 6.73661e-05 | 0.00580332 | intron-variant | USP40 | GRCh38.p7 | 2:233493395 | TCTCTTTATGATGCA[C/T]TGGCTGCTGAAATCC | 55230 |
rs546075899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233532991 | AGGAAAATAAAGGAG[A/G]AGATATGAAAAGATA | 55230 |
rs546129533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233542774 | TGGCTTTGAATTCCA[A/G]CTCCTGGTTGAGCAA | 55230 |
rs546184676 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, missense | USP40 | GRCh38.p7 | 2:233487888 | AAAGTAGAATAAGGG[A/G]GCAGAGCGACGGGAG | 55230 |
rs546225191 | snp | C/T | | | intron-variant, synonymous-codon | USP40 | GRCh38.p7 | 2:233487935 | GGATGGCAGACTGTC[C/T]GAACACACTGACAAC | 55230 |
rs546248149 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233533098 | AAATAAAGGAGAAGA[A/T]ATAAAAATAAGACCA | 55230 |
rs546289224 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233482133 | TGCTAGGAACATGTC[A/G]TGTCAAGTATTATAA | 55230 |
rs546295652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233555578 | TAGCTAAGTCAAGCA[C/T]GTAGTAATTCAAAGA | 55230 |
rs546399145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486958 | GAAACAGGAGGGACT[A/G]GAGGCCTCCTTGAGA | 55230 |
rs546436152 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233500617 | AAATGGCAAAAAAAA[A/C]CCCACCAAAATACAC | 55230 |
rs546462291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233487717 | GTGTATCTTTATTTA[A/G]TAAATAATTATTGAC | 55230 |
rs546498084 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233516654 | GATCGCACCACTGCA[A/C]TCTAGCCTGGGTGAC | 55230 |
rs546522700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233525687 | AATGAATACTCTCAC[C/T]CCCACCCAACACCGA | 55230 |
rs546523128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233493723 | TTACAATCAAAAATT[C/T]AAAATCATAAAAATC | 55230 |
rs546523392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233487108 | TACAACCATTGTGAC[A/G]AAGGGTCAAAATCAT | 55230 |
rs546533903 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233482598 | TTTTTTTTTTTTGTT[G/T]TTTTTTTTTTGACAC | 55230 |
rs546573581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233481686 | CCGTCAGTCTGTTCT[C/T]GCCTCTGTATTTCTA | 55230 |
rs546588491 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233539114 | CTTCCAGAAGATACA[C/T]GAAGCAAAAACTGTC | 55230 |
rs546607394 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233500779 | CAAAGTGATCCCATT[G/T]ATAATTTAAAAGAAA | 55230 |
rs546625394 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233506785 | GCATAGTAGCATATA[C/T]CTGCGATCCCAGCTA | 55230 |
rs546681094 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233531855 | GCGGACTTTGAGAAG[C/T]GATCGAAAAATCTTA | 55230 |
rs546721041 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233526729 | AGGGAGAAGAGGGAC[A/T]GAGTCCCAGCTCCAT | 55230 |
rs546751584 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233480313 | CAGGGCAGAAGCAGT[C/G]AGAATAGGACAAAAG | 55230 |
rs546810109 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233508830 | CTGCACATTTTTGTA[C/T]AGGATCATTATGAAC | 55230 |
rs546833882 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233547661 | ATAATTTCTTGGGAA[C/T]TAGACACCGGTTAGC | 55230 |
rs546850093 | in-del | -/A | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233475592 | CTCAATCCCCAAATT[-/A]AAAAAAACAGAAAAC | 55230 |
rs546854189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233547691 | CACTTTCCCTCAGAA[C/T]ATCTGCAAATTCTTT | 55230 |
rs546885860 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486279 | CCTGAGCAGGTACGA[C/T]GTGGCAGAGAGGGAC | 55230 |
rs546913134 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233509716 | TGTGGTAGTAGGTAA[C/G]TGTAATCCCAGCTAC | 55230 |
rs546923756 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233541375 | TTATCATAAGAAGAC[A/G]AAGTTTGGACAAAGT | 55230 |
rs546956985 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233567666 | TATAAGATTATAGCT[A/G]TATAACCTTATATAA | 55230 |
rs546972068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233564330 | ATATGGAGACACTGT[A/G]GAGAGCTGAGCTACA | 55230 |
rs546991050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233508120 | AGCAAATGCCAGATA[C/T]ATAATTTCATCTGTA | 55230 |
rs547000545 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233479245 | TGCTTGGAGAAGTCT[G/T]ATGAAGTCAGTGGCA | 55230 |
rs547017842 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | USP40 | GRCh38.p7 | 2:233560062 | CCTATTATAAGGGAA[A/C]AACTAATTATGATTC | 55230 |
rs547036448 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233516674 | GCCTGGGTGACAGAG[C/T]GAGACTCCATCTCAA | 55230 |
rs547066856 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP40 | GRCh38.p7 | 2:233519355 | CATGGACTAGATACA[C/T]ACCCACATCAGATAT | 55230 |
rs547073145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233553754 | GATGAATAAATTTGA[A/G]AAATGTCAGAATTCT | 55230 |
rs547135530 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP40 | GRCh38.p7 | 2:233550639 | CTAATAAATGTTCTA[C/T]TCTGAATAAACATAT | 55230 |
rs547248315 | snp | A/G | 5.02155e-05 | 0.00501051 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527470 | GGTCAAATCCCACAC[A/G]CTTTCTGTTTGAGAG | 55230 |
rs547252293 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233549953 | AAAATAAAAAGCTAA[C/T]TTAGATTAAGAGATA | 55230 |
rs547362229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233515428 | TCCACTGGGTGCACA[A/G]TAGGGTGTCATTTGG | 55230 |
rs547362256 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233523934 | GTGCAGTTCTTCACA[C/T]GACGAGGGCCTAAAA | 55230 |
rs547423924 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233542310 | CAGTGGATGATCAAT[C/T]TCTTCTTCACTCTGG | 55230 |
rs547426537 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233557412 | GCACATGTGAATAGT[A/C]CGAATTATCAACAAT | 55230 |
rs547491418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233551311 | AACCAACTGAAAATC[A/G]GGTCAATAATAGATT | 55230 |
rs547648133 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233517451 | GAGCAGTGGCGCGAT[C/T]TCGGCTCACTACAAG | 55230 |
rs547704126 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233549045 | ATTTCCTCAACAAAA[A/T]AATAGGAATAGAAAA | 55230 |
rs547720851 | snp | C/T | 0.000399281 | 0.0141238 | missense, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233562755 | GCATCGGGTTTATCC[C/T]TATCTTCAAACAAAC | 55230 |
rs547731041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233555749 | CAAGCGATTCTCCTG[C/T]CTCAGCATCCTGAAA | 55230 |
rs547765010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233478667 | ATGGTGACAGATTGG[C/T]GACAGCCTGGAAGTG | 55230 |
rs547805315 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233502617 | AAGTGTGGCAGTATC[C/G]CCCTCCCCAGAGAGA | 55230 |
rs547891943 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP40 | GRCh38.p7 | 2:233515724 | TCTTCCATGGTTTGT[A/G]CTTTTTGAGTCCTAT | 55230 |
rs547925165 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233510310 | AGCAATAATTATGCC[A/T]ACCCAGAAGTATAAA | 55230 |
rs547951589 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233561333 | TACTACAAGGGTACA[A/G]TAACCAAAACAGCAT | 55230 |
rs547955049 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233478057 | CCACCCACGCTGCAC[A/T]GTCCCCGACAGAAAG | 55230 |
rs547960492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233511594 | TAAAATAAAATGTAT[A/G]ATTTAAGAAAAAACT | 55230 |
rs547996245 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233480064 | CCCTTCACACCCTCC[A/G]GCAGCCTCTAACCAC | 55230 |
rs548015417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233555236 | AAGAAGGTCTTCCTA[C/T]GAAAATCCAAGAGAA | 55230 |
rs548026792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233503607 | AACCTTGCAGGCCAG[A/G]AGAAAATGGGGGTAA | 55230 |
rs548050009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233478137 | ACGGCCAGAATCTGG[C/T]CATGGTGAATGAAGC | 55230 |
rs548082392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233488388 | CAATTTTAAGCTTTT[C/T]TCTTAAGCAAAGAAT | 55230 |
rs548089719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233556136 | AAAAAAAAAAGAAAA[C/T]GGTAATTTTGTCCTG | 55230 |
rs548090264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233483068 | TCTGCTGTGTTACTG[C/T]GTATGTCGCTCCCCT | 55230 |
rs548114332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233533997 | GACATCCAGGGAGGA[A/G]GTCGCTATGCCACAA | 55230 |
rs548217165 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233555688 | GCCACCAGGCTGGAG[C/G]ACAGTGGCGCAATCT | 55230 |
rs548229595 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233548979 | CTGTATTAACTTTCA[C/G]TGCCTATCAAAGTTT | 55230 |
rs548266417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233556301 | CAATTTCTAATTTCC[A/G]ATTAGATTAAATGGG | 55230 |
rs548300178 | snp | A/C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233509607 | GCACTTTGGGAGGCC[A/C/G]AGGCGGGTGGATCAC | 55230 |
rs548312440 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233512229 | GAGGTGATACAGAGA[C/T]GAGAACTGAAGATTT | 55230 |
rs548324186 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233484589 | TCATCCCTAGCGATC[C/T]TCCTACCTCAGCCTC | 55230 |
rs548327992 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233549692 | GTCCTCTATTTCAAC[C/T]AGGTTGTCATGTGCC | 55230 |
rs548382957 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233542183 | CCTAGCAATTAAACC[A/G]CATACATTCTTACAT | 55230 |
rs548455444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233534685 | AACAGAGGGTAAAAC[A/G]GCCTTGCAGCTAGTT | 55230 |
rs548496229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233526858 | CCAAATCACATGATT[C/T]ATATGAAAGCAGTGT | 55230 |
rs548513246 | snp | A/G/T | 0.000195298 | 0.00988017 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485946 | TCTCACCAGGGATGC[A/G/T]CACCTGTGTCCTCAG | 55230 |
rs548579452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233517530 | GCTGGAACTACAGGC[A/G]CACACCACCACGCCT | 55230 |
rs548603162 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233548494 | GTCTCTTTATGATAA[A/T]GGAGTAACTGTATAG | 55230 |
rs548606290 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233545534 | AAGTCCCCCCAGGAA[G/T]CTGGTGGCATGGATC | 55230 |
rs548617277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233541640 | ATAATTAAAGTACTC[A/G]ACCCAGGTCCCTAGC | 55230 |
rs548734878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233521811 | CCAAATAAAACAAAG[C/T]ATGAAGCACAAGATG | 55230 |
rs548750024 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233568764 | GATGCACTATCCATC[A/T]AAGGTGCACTTTGAG | 55230 |
rs548788997 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233509348 | TTTACTTTATCACAT[A/G]CACACATATATACAA | 55230 |
rs548800029 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233538491 | CAGAAATGAAAAAGG[A/C]ATCATAAGTTCATAT | 55230 |
rs548825401 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233555905 | AGATCATGAGGTCAG[A/G]AGATCGAGACCATCC | 55230 |
rs548840895 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485712 | TGAAAAATTGCATAA[A/C]CTCATTGCTATGCCG | 55230 |
rs548846024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233477606 | TTTTATAGGCCACAA[A/G]GACGTGCATTTGCAA | 55230 |
rs548867966 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233525813 | GGCACAACAACCATC[C/T]AAACAATTCTGCTTA | 55230 |
rs548890122 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233565299 | GATTTTGCATAATTA[A/T]TTACATGTAAAGAAG | 55230 |
rs548923249 | in-del | -/AAGAAG | 0.00398564 | 0.0444627 | intron-variant | USP40 | GRCh38.p7 | 2:233502951 | TGAAGATATCAACAT[-/AAGAAG]ACAAGAAATATGAAG | 55230 |
rs548935977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233528179 | AGATGGGGTTTCACC[A/G]TGTTGACCAGGCTGG | 55230 |
rs548956338 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233539253 | AAGAAACAAAGAACA[C/T]AATCAATTTGACCTA | 55230 |
rs548960472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233490052 | CAATATTCATCCATT[C/T]TTTGACCTAAAAACA | 55230 |
rs548988406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233505714 | AAGCTGAGGACCTAA[C/T]GGCTTCACTGCTGAA | 55230 |
rs549021343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233490959 | AAAGCACAGCATGCC[C/T]GTCAGAGGAGGGACC | 55230 |
rs549108258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233484163 | ATACTGTCTCAACAA[C/T]AACAACAAAAGAAAA | 55230 |
rs549122264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233496067 | AATCAGCTAACTGTG[A/G]CTCTCTCTGCAGAGA | 55230 |
rs549182725 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233475652 | ACGCACAGGCCGGCC[C/T]GGCCGCACGCGCCTG | 55230 |
rs549185382 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233497032 | GGCATAAGCTGTAAG[A/T]CTGACAGAAGAACTG | 55230 |
rs549206998 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233566042 | TCTGCTTGTCACACC[C/T]TTCAGTACTATATAC | 55230 |
rs549219408 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233558454 | TGAAGTATCGACACA[A/T]ACTACAACATGAATG | 55230 |
rs549239788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233514505 | AGTGAGTTGTGAGTA[C/T]GCAGAAAAGCAGATC | 55230 |
rs549299679 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233544025 | ACAGCACAGACTCCA[-/T]TAAGTTGAGGACTCA | 55230 |
rs549304885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233506319 | TAATGAGACTAGATT[C/T]CCTAACTCTCACTAA | 55230 |
rs549345979 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233552766 | GGGTTTAAGGTTTTA[C/T]TATAGTTTTATCTAT | 55230 |
rs549405678 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233558295 | AAAAAAATTTTCACA[C/G]CATTAAGAAGAAACC | 55230 |
rs549408585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543870 | TTGATGCCCATACAG[A/G]GCAGAGTTGGGGAGA | 55230 |
rs549420782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233535910 | ACTTCACCACAAAAA[A/G]TAAGTATTTGAGATG | 55230 |
rs549425026 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233563279 | ATAACAGATGGCAGT[A/G]GTCTTATCTGGAAAA | 55230 |
rs549549249 | snp | G/T | 3.67478e-05 | 0.00428632 | intron-variant | USP40 | GRCh38.p7 | 2:233551339 | ATTCAATCTTGAGAG[G/T]GGAAAAGAAAGAATT | 55230 |
rs549628635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233565127 | AAAAAGAAATATATT[A/G]CTTTATTTTTTTACT | 55230 |
rs549683542 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233553513 | CAATATGTGGCAGAG[C/G]GATTTTCAGAAATGC | 55230 |
rs549752393 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475172 | TTATTTTATTTATGT[A/T]TTTTTTTTGAGACGG | 55230 |
rs549759856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233505529 | ACATACAAAGGATCA[C/T]AAGAGACTATTATGA | 55230 |
rs549799520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233551757 | GGTTTTATCTTTAAT[A/G]TTGATATCCTGAAAT | 55230 |
rs549851598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233535736 | ACAATATGAGATTAT[A/G]TGGAGCAGGGGGGCA | 55230 |
rs549860294 | in-del | -/TTC | 0.0023933 | 0.0345097 | intron-variant | USP40 | GRCh38.p7 | 2:233541546 | TGTCAGAAAATACAT[-/TTC]TATCATCTAAGCCAT | 55230 |
rs549871290 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233490551 | ACAACCACTAGTCAT[A/C]TATAGGCCCCACATT | 55230 |
rs549897457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233488864 | TTGAGCCATGATCAC[A/G]CCACTGCACTCCAGC | 55230 |
rs549912956 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233511482 | CTCAGCATCAAAGAT[A/T]CCTTTTAACCACAAA | 55230 |
rs549923444 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233502729 | TCACAAACACCCGTA[A/C]CCTAGGAAATTGAGG | 55230 |
rs549938975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233498404 | AAAAACTATAGTAAG[A/G]AAAAAGTAAAATAGA | 55230 |
rs549980237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233479302 | AGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGT | 55230 |
rs550003087 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233475568 | TTCTTTAACAAAATC[A/G]TACAGCTTTCTCAAT | 55230 |
rs550005804 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233509871 | AAAAAAAATCCAGTT[-/G]GTTCACCAATTTTCA | 55230 |
rs550150450 | snp | C/T | 0.000228232 | 0.0106801 | intron-variant | USP40 | GRCh38.p7 | 2:233489346 | AGAGGGACAGTGTTG[C/T]GTCCAGCAAGGAACC | 55230 |
rs550174845 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543828 | AATGGACTAAGACAC[A/C]GATCTTGCTGACACT | 55230 |
rs550192513 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233532014 | AACACAAGGACCAGA[C/G]GCTACTTCCTTTGAC | 55230 |
rs550202054 | snp | C/T | 0 | 0 | intron-variant | USP40 | GRCh38.p7 | 2:233483621 | TGGTGTGAGCAGAGG[C/T]AAGTACAGGTTTTAT | 55230 |
rs550264377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233525147 | ATCAAGTCACATAAA[C/T]ATGATTCAGATGGTT | 55230 |
rs550268634 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233489823 | CACCAGGGCAGAGCC[C/T]GCTCTAACAGTACAA | 55230 |
rs550297355 | in-del | -/ACCTGT | 0.00517822 | 0.0506191 | intron-variant | USP40 | GRCh38.p7 | 2:233518153 | ATGTAACCAAACACC[-/ACCTGT]ACCCCAATAACCTAT | 55230 |
rs550299846 | snp | C/G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233493998 | ATACATACCCTGTAA[C/G/T]TTCAGTTTTACTTAT | 55230 |
rs550316234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233487018 | CAGAAAAGCCCATGG[A/G]AGGGGCCTGAGGAGG | 55230 |
rs550377037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233563349 | ATCACCCAACATCTA[A/G]GTGATGTGCCACCCA | 55230 |
rs550382784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233499793 | CACCCTATAAATTTT[C/T]TTTTCCTACAACCCT | 55230 |
rs550393350 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233556349 | AAGAACTGAAGGTTA[C/T]ACTAATTAACATAGG | 55230 |
rs550410098 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233529377 | GCTTAAGGCCTAAAT[C/G]AGATCTTTATTCTCC | 55230 |
rs550477771 | in-del | -/TTATAT | 0.00159617 | 0.0282053 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233568550 | TATAAAGATATAAGA[-/TTATAT]TTATATAATCTTATA | 55230 |
rs550538816 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | USP40 | GRCh38.p7 | 2:233480427 | TGGAGCTGATGCCAC[G/T]GGCAGGTCCTGGGAC | 55230 |
rs550544564 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476143 | TGAGGGACAAAGCAG[A/G]CCGCTGGCTCAGCAT | 55230 |
rs550550097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486564 | ACGTGCAGAGGTCAG[C/T]ACAGGCCATGGAGGA | 55230 |
rs550602176 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476499 | ACATTTTCTTTTTCT[C/T]AGGTGTTTTCATTGA | 55230 |
rs550603137 | snp | A/G | 0.000299967 | 0.0122431 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233481225 | TTCTCCCCAGGGCCC[A/G]TTGTTTCTGCTTTTC | 55230 |
rs550614614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233547588 | TACATCCTAACATTA[C/T]GGTTTGTGACTTACT | 55230 |
rs550624996 | in-del | -/GTGTA | 0.00279162 | 0.0372561 | intron-variant | USP40 | GRCh38.p7 | 2:233513306 | TACTTTTGTTTCTTT[-/GTGTA]CTTTCTTCTCTGTTG | 55230 |
rs550654367 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562659 | AGCATGGCACATGTA[C/T]ACATATGTAACTAAC | 55230 |
rs550760900 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233567346 | TAACCTTATATAAGA[G/T]TATAGCTATATAACC | 55230 |
rs550778892 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233517043 | TGCTATTATAAATGT[C/T]TTCTTAATTTTGATG | 55230 |
rs550802984 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233547103 | GGCAAAGGATTTGGA[C/G]AGGTAAAACAAAACT | 55230 |
rs550833094 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233480116 | ATGGTCACGAGGTCA[C/T]GCTCACCTGCCCTGC | 55230 |
rs550833670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233553659 | CTCTCATTTCTCCTC[C/T]TATCAAAGTATCTCT | 55230 |
rs550834505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233515856 | GATCCATTTAATTTT[C/T]GCATCAGGCGAAGTA | 55230 |
rs550868646 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233540044 | GCAGGAGAATCACTG[C/G]AGCCTGGGAGGTGGA | 55230 |
rs550889071 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233492458 | TTATTTACTTTTCAC[A/G]TAGAAACATACTGAT | 55230 |
rs550937812 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | USP40 | GRCh38.p7 | 2:233539143 | TCAAAACTTTTTTTT[A/T]AAAAAATGAGACAAA | 55230 |
rs550990133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233539058 | CATTTCACGCCAGGA[A/G]GCAATAACAATCCTA | 55230 |
rs550995832 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233522151 | AGTCTACAAATCTCA[A/G]GGTTGGGCAGGGGTA | 55230 |
rs550998392 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233490317 | ACAGGTGCCTGCCAC[C/T]GTGCCAGGTGAATTT | 55230 |
rs551030380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233515334 | CCATTTTACCTTCCC[A/G]TCAGCAATATATGGG | 55230 |
rs551058275 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233559177 | TCATTGCTGACAAGT[A/G]TGTAGTGTTCGTATA | 55230 |
rs551059624 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233539591 | ATGAAAGCTTGTTGA[A/C]TATAACTGACTATAT | 55230 |
rs551081877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233499644 | TGTAAAACATTCCTA[C/T]TTTGTACCTTTGCTG | 55230 |
rs551121118 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233515256 | GTAAATACCTAGACG[G/T]AGAATTGGTAAGTGG | 55230 |
rs551144760 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233504947 | ATCCATGATAGAGCA[C/T]ACATTAGACCACAAA | 55230 |
rs551152588 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233490899 | GTTTCCCTAAAAAAA[C/T]AAAAATGAACAAAAG | 55230 |
rs551267827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233558536 | TTGGATCACTCCATT[C/T]CTATGAAATGTCCAG | 55230 |
rs551283558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233538946 | AGCTAGGAGGATCAC[A/G]TGGGCCCAGGAGGTC | 55230 |
rs551285220 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233492345 | AATGATGAAATCATC[G/T]GACGATGCATTTCTC | 55230 |
rs551297721 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233531163 | GAGCTACCTTACCAC[A/G]GATTAAAACACAAAT | 55230 |
rs551333915 | snp | C/T | 0.00110558 | 0.0234855 | intron-variant | USP40 | GRCh38.p7 | 2:233560967 | AGTAGCAGTATTGTA[C/T]TTGGAAAACTGATTC | 55230 |
rs551338414 | snp | A/G/T | 0.000110093 | 0.00741859 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485503 | TCGTGTCTTCTCAAA[A/G/T]TGGTAAATTTGCTGT | 55230 |
rs551345858 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233491789 | ATAAGGAAATCTTGA[A/C]AATAAGAAGGCCTTT | 55230 |
rs551390993 | snp | A/C/G | 0.00517822 | 0.0506191 | intron-variant | USP40 | GRCh38.p7 | 2:233529045 | ATCCTCTCTCACTAC[A/C/G]TGCCAGTTCGCTACA | 55230 |
rs551406931 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233553555 | TATAATAAATCCCTG[A/C]CATATCAGAAAGGAG | 55230 |
rs551418736 | in-del | -/GAGGC | 0.0032064 | 0.0399114 | intron-variant | USP40 | GRCh38.p7 | 2:233555120 | ATTGCTTGAACCTGG[-/GAGGC]GGAGGTCGCAGTGAG | 55230 |
rs551461944 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233479705 | CAGCCAGCGCTGCAG[C/T]CCCTCTCCCATATCC | 55230 |
rs551563711 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233490127 | TTCCCATTTGTTCTC[A/T]TGAGAATAAGGCTGT | 55230 |
rs551631601 | snp | A/G | 0.000208167 | 0.0102 | intron-variant | USP40 | GRCh38.p7 | 2:233523163 | TTTTCTCTTGTTAGC[A/G]AGTTACCTGTTATCA | 55230 |
rs551727453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233530374 | ATAATTAACCTAACC[A/G]ATCTTTTTCTGTTAG | 55230 |
rs551733529 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233481363 | TACATTTAAAAGAGG[C/T]ATGTCTAAAAAACTA | 55230 |
rs551797595 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233529143 | GGCCAGGATACAATT[C/T]ATTCAGCCCAACTAT | 55230 |
rs551798505 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233478082 | AGAAAGCCTCCGCGG[C/T]CCACCCGCCATCCCA | 55230 |
rs551837957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233521920 | TTAGCACTTACTGTG[C/T]GTACTTTGTAAGCAC | 55230 |
rs551852627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233526798 | TTTAAATCACACTGC[C/T]TCAACTTCAAAATGG | 55230 |
rs551905142 | in-del | -/C | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476496 | TTACATTTTCTTTTT[-/C]CTCAGGTGTTTTCAT | 55230 |
rs551944782 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233497618 | AAGCCAGTTCCAAGG[A/G]TAATGAGTTGGCTTC | 55230 |
rs551962509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233518486 | GCAGAAAAATTGCTT[A/G]AGCCTGGGAGACGGA | 55230 |
rs552007621 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233504426 | AAGACAAACATAGAC[C/T]GAAAGTGAAGGGATG | 55230 |
rs552020912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233482289 | GAGTCACTTGAACTC[A/G]GGAGGTGGAGGTTCC | 55230 |
rs552101199 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233537329 | TTCTAGAACCAATCC[C/G]CCATAGATATGGAAG | 55230 |
rs552115324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233538227 | AGGAAAAAGAAAATA[A/G]AGAATAGAGGAGAAA | 55230 |
rs552131386 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233477743 | TGGTTCAGGCTCTGG[A/G]GCTTTCTCAATCTGC | 55230 |
rs552132647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233560939 | AGTAAAGAGTGTTAC[A/G]TGTTTATAAAGCAGT | 55230 |
rs552164336 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233478367 | CTTTAGTGTTGCCAA[C/T]AGGCATGTGGCACTG | 55230 |
rs552177181 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233557933 | CAGCAGGATGCCTTG[-/A]ACCCAGGGCTGCAGT | 55230 |
rs552186284 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233480608 | TGCAGAGCCAGACAA[C/T]GGCAGGCGGCGCCAG | 55230 |
rs552196214 | snp | A/G | 0.000472701 | 0.0153664 | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233561241 | TCATATGGAACCAAA[A/G]AAGAGCCCGCATCGC | 55230 |
rs552266756 | snp | A/T | 9.92704e-05 | 0.00704452 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562848 | AATGACATCATTTCA[A/T]TTTAAAAAATTGTTT | 55230 |
rs552470628 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233482602 | TTTTTTTTGTTTTTT[G/T]TTTTTTGACACACGG | 55230 |
rs552502263 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233533911 | GACCTGGCCAGCTAC[A/G]GGGGAAAATCCATCT | 55230 |
rs552553681 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233500925 | TTATCTGATTGCAAC[A/C]GTGACTTCTAGAGAA | 55230 |
rs552555234 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP40 | GRCh38.p7 | 2:233509096 | AGAAAATGGTATTTG[A/G]CAGCCATAATCTGGG | 55230 |
rs552648263 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233541901 | AATGACAATAATAGC[C/T]AAAAAAGTCATAACC | 55230 |
rs552711862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233523997 | GCATCTGACGCACAA[C/T]CTGGTATAACGGAGG | 55230 |
rs552752824 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486611 | ACTGGAAGGCAGCAA[C/G]GGGAAATGAAGACTG | 55230 |
rs552844962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233523729 | CATTTATGAGTTATC[A/G]TGGGTGGTGATGAAG | 55230 |
rs552929550 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | USP40 | GRCh38.p7 | 2:233540087 | CTGAGGTCGTGCCGC[C/T]GCACTCCAGCCTGGG | 55230 |
rs553010369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233508610 | CTAGCAATCTTTGAG[A/G]ATCCTTGCCTAGGTT | 55230 |
rs553022949 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233532638 | GTCTAATTCTTTGTT[C/T]GAAATGCCAAGAACC | 55230 |
rs553076677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233559255 | ACATACAACAAGATT[C/T]ATAAAGAAAATGGAG | 55230 |
rs553111286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233499185 | CACCAACAGGCCCCA[A/G]TGTGTGTTATTCCCC | 55230 |
rs553119356 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233478300 | TCCACACCCACACAC[-/AG]GGGATGAGAGCCCCA | 55230 |
rs553134828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233480799 | AACCTTGGAGAGAGC[A/G]GGAGAAGGACAGGGA | 55230 |
rs553135289 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP40 | GRCh38.p7 | 2:233495988 | CATTAAAAAGGATAT[A/G]CACATATTTGCCTTC | 55230 |
rs553262677 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233514141 | TTGGCTACGTGCCAG[A/G]CACTGTGCTAGAAAC | 55230 |
rs553286042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233498730 | TTTCCAGATAATAAA[A/G]CTATGGGCCTCCATG | 55230 |
rs553289090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233480148 | ACCTCCACCTGGGAC[C/T]TCTCTTCCCCAGACG | 55230 |
rs553349292 | in-del | -/A | 0.0197687 | 0.0974348 | intron-variant | USP40 | GRCh38.p7 | 2:233549293 | GATAATAATCAAAAG[-/A]AAAAATAATTTCAAC | 55230 |
rs553391492 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233492449 | AAGAACCTTTTATTT[A/G]CTTTTCACGTAGAAA | 55230 |
rs553440852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233495371 | ATTGTTTGAAATTAA[A/G]TGTTGTAACAGTAAC | 55230 |
rs553455866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233539208 | CAGTAATTAATAGAA[A/G]AGGCAAAAAAAAAAA | 55230 |
rs553460993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233546678 | AAAAAATGAACACCA[C/T]AATAAACACTTACCA | 55230 |
rs553476711 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233488934 | AGAAAAGGAAAGAAA[G/T]GAAAGAAAGAAAAGA | 55230 |
rs553575553 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233522271 | TGCATGCTGAGAAGA[C/T]GGATACTGTTTTGGG | 55230 |
rs553600466 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233535343 | GAGATAGCAAACTTT[G/T]TCTTAAAGAGCCAGA | 55230 |
rs553638525 | in-del | -/T | 0.00319169 | 0.0398203 | intron-variant | USP40 | GRCh38.p7 | 2:233531635 | GAAAAATACAAAGCC[-/T]TTTTCATTAACAGCA | 55230 |
rs553686710 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233514854 | TCTGGTAACCACCAG[C/T]AAACTGAGGTATAGT | 55230 |
rs553691383 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562984 | AACCAGTGACTCTAA[G/T]AAAATAGTGTCATGC | 55230 |
rs553708679 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233556329 | GGGCAATATGTGTCA[A/T]TACAAAGAACTGAAG | 55230 |
rs553743598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233496264 | TAGAAAGTAGTGCTA[C/T]GCGATGCTTACGAAA | 55230 |
rs553750491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233555973 | TACAAAAAATTAGCC[A/G]GGCATGGTGGCGGGC | 55230 |
rs553844001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233542653 | ACTGCACTCCAGCAT[A/G]GATGACACAGAGCAA | 55230 |
rs553856487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543362 | TCTTAAACACACCAT[A/G]AGCTTGCAAGAACAT | 55230 |
rs553910604 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233478185 | GATATCCTGGTAGGC[A/C]CGCGTCCATGTTTTT | 55230 |
rs553913240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233533339 | TCATTTGGCATAATA[C/T]AGTTCTTGTTAGCTT | 55230 |
rs553927283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562380 | CCATGGAATACTATG[C/T]AGCCATAAAAAATGA | 55230 |
rs553931951 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543996 | AATTGTATTCAATTC[A/T]GACACTATCAGGTGA | 55230 |
rs553973230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233510693 | ACAGATGTGAGCCAC[C/T]GCGCCCGGCCAACAT | 55230 |
rs553983098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233518596 | AAAAAAGATAATCAC[A/G]ATTAATCACAGATTG | 55230 |
rs553991737 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233548033 | GAAAAAAATGAACAA[C/T]GGAATAGAATAGAGA | 55230 |
rs554007976 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233481635 | CACGGATCTCTCATC[A/G]CCGCGCCAGAAGCAC | 55230 |
rs554027635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233501320 | GGTTTGAAAATATAA[C/T]AAAAATGATACCAGA | 55230 |
rs554064888 | snp | G/T | | | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551512 | GGCAGCTTACGTAAT[G/T]TGGCCGACTGTTAAA | 55230 |
rs554099500 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562431 | GGACATGGATGAAAT[G/T]GGAAATCATCATTCT | 55230 |
rs554119484 | snp | C/G | | | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233512476 | ATCAGTTTCCAAAAG[C/G]TAATTTTTAAATATT | 55230 |
rs554187207 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233522423 | TAATAGTGGTAAGTG[C/T]ACTACGAAAGAAACG | 55230 |
rs554198545 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233481816 | TGCATTCCCGTGACT[G/T]GGCAAGCCTCCTCCC | 55230 |
rs554201292 | snp | C/T | 0.000238834 | 0.0109252 | intron-variant, synonymous-codon | USP40 | GRCh38.p7 | 2:233487956 | CACTGACAACAGCTG[C/T]GGGTGGGCCTCTTGC | 55230 |
rs554248513 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233519039 | TGTTTTATGATTCCA[A/G]TTACATTAAACATTA | 55230 |
rs554250109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233527039 | GTATAAAGTTAGTTG[C/T]GTTTATTTGTTCAGC | 55230 |
rs554290343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233495179 | CACAGCATACACTAG[A/G]AGATAAAATATTAAT | 55230 |
rs554326385 | in-del | -/CTGGGCAGCCTCTCGCCTCGCCCTCCTCAGA | 0.0244538 | 0.107838 | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233566583 | CGTCCTCAGGCAGGC[lengthTooLong]CTGGGCCACCAACAC | 55230 |
rs554351535 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233477810 | TCCGTACTTTTTAAA[C/T]GGAAGAATAACATCC | 55230 |
rs554424201 | snp | C/T | 1.71699e-05 | 0.00292996 | intron-variant | USP40 | GRCh38.p7 | 2:233493384 | GTCAATTTACTTCTC[C/T]TTATGATGCACTGGC | 55230 |
rs554495088 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233549022 | ATATATAATAAATGG[C/T]AAACAAAATTTCCTC | 55230 |
rs554534117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562941 | TTTATACCTTACTCT[A/G]TACACTTTACTTTCT | 55230 |
rs554536529 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233487599 | ACTCATATCATAATA[C/G]GTAGAGCAAATCTTA | 55230 |
rs554541062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562276 | CACACGTATGTTTAT[C/T]GTGGCATTATTCACA | 55230 |
rs554561442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233517877 | TTAATGGCATTTGCC[A/G]TGACCTAGATGAGAT | 55230 |
rs554642594 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233492801 | AGAGTTGGGCCTATT[-/A]AAAATATACTCGCTC | 55230 |
rs554655509 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233555925 | CGAGACCATCCTGGC[C/T]AACATGGTGAAACCC | 55230 |
rs554718099 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233517201 | TGGATATGGTGATTA[C/G]GGAACACTTCAACAC | 55230 |
rs554731030 | in-del | -/TGAG | | | intron-variant | USP40 | GRCh38.p7 | 2:233511311 | AACCTAAAATGCTAC[-/TGAG]TGTTAGACTTACTAT | 55230 |
rs554787583 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233547198 | TTGTTTAATATTTTA[C/T]ATATTTTGGTATATA | 55230 |
rs554802461 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233481899 | TGTCCACAGGGAGGA[C/T]GCCTCAGGGGCGCAC | 55230 |
rs554833603 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233526159 | CTACAATACCATAAG[C/G]TATTTTCTTAAAAAG | 55230 |
rs554835265 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233508387 | CCCTGCAATTTATCT[C/T]TTGTAGAAGAGTTTT | 55230 |
rs554886560 | in-del | -/ATTTC | 0.0023933 | 0.0345097 | intron-variant | USP40 | GRCh38.p7 | 2:233531027 | ATTAAAGGAACTATA[-/ATTTC]ATTTAAGTGATTTGT | 55230 |
rs554907459 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486812 | CACAGCCCCATGTCC[C/G]CATGGGGGAGGGGGC | 55230 |
rs554919819 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233518522 | CAGTGAGCGGAGATC[A/G]TGTCACTGCACTCCA | 55230 |
rs554949853 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233540748 | GGCCCAGCTGATCAA[C/T]AGGAATTAGATTATT | 55230 |
rs554985809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233547976 | GATCAAGACTTATTA[C/T]AAAGCTATGGAAATT | 55230 |
rs555058106 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233484370 | TTCTTTAACACTGCT[A/C]AGTATGTTTTTGTAT | 55230 |
rs555079806 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233551148 | GGTTGTCACAACTGA[A/G]AGAGGGGGAGTGAGG | 55230 |
rs555107920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233525448 | TGTAGATATATAGAG[C/T]GAGTTGCTATGTTTT | 55230 |
rs555118005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233533314 | TTATAAAATGACAAA[C/T]TGTTAGATTTCATTT | 55230 |
rs555186304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233550902 | AACTAAATCCAAATT[A/G]GTGGTACCAATTAAT | 55230 |
rs555204381 | snp | C/T | 1.73165e-05 | 0.00294244 | splice-donor-variant, intron-variant | USP40 | GRCh38.p7 | 2:233551375 | ATAAAATAGTTCAAA[C/T]CTGTTCACAAAAGGG | 55230 |
rs555267645 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233545090 | AAAGCAAGAAGCCTA[C/G]AGTCCACAATACTAA | 55230 |
rs555319922 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233483824 | TGAATCATAGATACT[C/G/T]AACTTGTATAAAATT | 55230 |
rs555335460 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233544424 | ATTAAATAAATCACT[C/T]GTCACTGGTGACTGA | 55230 |
rs555346919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233492779 | ATAAAAAGAAAAACA[C/T]AGCTAAAGAGTTGGG | 55230 |
rs555361296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233490273 | GGTTCAAGTGATTCT[C/T]CTGCCTCAGCCTCCG | 55230 |
rs555364731 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233484911 | TGTTGTTTAGTACAG[C/T]GTTAAACAGAAGGGG | 55230 |
rs555373120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233537586 | AAAAAGAAACATTAC[A/G]TTCAAGAGAATGAAA | 55230 |
rs555381910 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233500354 | CTGTCTGAATTTCCC[C/T]GTTTTCCCTAAATAT | 55230 |
rs555411364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233556521 | ATTTTTATTACCTCC[C/T]TAATTAACTTTCTTT | 55230 |
rs555454482 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233531601 | ACCAGAACCATTTCC[A/C]TATCTTTTTTTCCTC | 55230 |
rs555466007 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233555124 | CTTGAACCTGGGAGG[C/T]GGAGGTCGCAGTGAG | 55230 |
rs555501129 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233520369 | GTGTAAATATTAACA[C/T]ACTTTAAGAAATTAT | 55230 |
rs555510413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233521514 | GACACTGCACAAAAG[A/G]GCCACATCTAAGGAG | 55230 |
rs555521814 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233557079 | TTTTAAAACATTAAA[A/C]AAACAAACATTAGTC | 55230 |
rs555529408 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233495494 | ATTCCTGAGCTCAAG[C/T]GATTTGCCTGCATTG | 55230 |
rs555559993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233511916 | AAGAAGAAAAATGAG[C/T]TGCACTTCAGACAAA | 55230 |
rs555637392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233527236 | GTGGAGAAAAGCCTC[C/T]CTAAAAGACTTAGGA | 55230 |
rs555647423 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233527778 | CCATGAATTCCAAGA[G/T]AAAACTGTTTTAACA | 55230 |
rs555706761 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233483361 | CCGGGCATAATGGCA[C/T]GTGCCTGTGGTCCCA | 55230 |
rs555728211 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233489794 | TTGGAATTAACTTCC[A/G]TGGGAGTAGAATTCA | 55230 |
rs555744617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233497812 | GCCTCTTGCTATTGA[C/T]TTACTGACTGCTAAA | 55230 |
rs555797722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233478891 | CGGTCACGCTGGCCC[A/G]TCTAGGAGAGGCTGT | 55230 |
rs555847399 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233489007 | TTTGCAAAGGAAATG[A/T]CCCAAACCTGCTCTT | 55230 |
rs555872525 | snp | A/G | 7.90108e-05 | 0.00628483 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233512600 | CCCATTTCTATCAAT[A/G]GGTCTCAAACAGCTG | 55230 |
rs555927932 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233563808 | TGTGCACTAAGATGT[C/G]AAATCATATGCTTGG | 55230 |
rs555987031 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233504143 | GTAACCACAAAGAAA[A/G]ACATGACAGAAAATA | 55230 |
rs556021682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233535268 | AGGTTCAATATCTGA[A/G]CAGGGCTGCCTGATG | 55230 |
rs556069707 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233524569 | GTTCATCCCCTAGAA[A/G]GAGATCACCAGTGAG | 55230 |
rs556103753 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233512715 | AGCTGGTTACAGCAT[C/T]AAACACAGAAAACAA | 55230 |
rs556108334 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233527317 | AAGCAGCTTTGAAAA[A/G]TAAAGTTGTATCCTA | 55230 |
rs556130917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233478326 | GCCCCAGTGACTCTG[C/T]GTCCTCAACACACGA | 55230 |
rs556146834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233489676 | CCCTGAGCGGTCTTC[A/G]TATTCCTCTGCACTG | 55230 |
rs556155402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233497312 | TAACCACAGGACATG[A/G]AATAGAAATAAAGGA | 55230 |
rs556264929 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233563145 | TCAGGAAATACAGTA[G/T]TGTTGCAGTTTTCCT | 55230 |
rs556309457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233527106 | TTTCACTCTCTTTGA[A/G]AGGCAATTTGCTTTC | 55230 |
rs556316804 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233485295 | GAATTTTCCATGTAT[G/T]GTCAGAAGTGAAACT | 55230 |
rs556372716 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233518691 | TTTGGATAATAGTGC[A/G]AGAGTTTCTTATAAA | 55230 |
rs556441266 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233494061 | GTGAAGAATTTTAAC[A/G]GGTTTATTAAGAGAT | 55230 |
rs556452452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233534418 | CTCTCACTCTTTAAC[C/T]TCTGTCTGGCCTTGA | 55230 |
rs556569137 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233523612 | AAAATAAAATTTTCA[A/C]AAATGTCTGTTAAGC | 55230 |
rs556601481 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233478291 | TGTGCCAATTCCACA[C/G]CCACACACAGGGGAT | 55230 |
rs556619674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233519201 | CTACACATTTACTGA[C/T]GATTACTGAATTAAA | 55230 |
rs556649324 | in-del | -/AC | 0.00398564 | 0.0444627 | intron-variant | USP40 | GRCh38.p7 | 2:233547323 | CATGTTCCTGGTAGA[-/AC]ACAGTTTGACTTTTT | 55230 |
rs556661093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233478865 | AGGTCTCTGAAAGGA[C/T]ATGCAGGTGACGGTC | 55230 |
rs556684724 | in-del | -/ATAA | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233533006 | AAGATATGAAAAGAT[-/ATAA]ATAAAGGATAAATAA | 55230 |
rs556703931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233511088 | AGTCCAGATTACCCT[A/G]CTACAGGGTATTCAC | 55230 |
rs556716875 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233544437 | CTCGTCACTGGTGAC[C/T]GAACTCAATTTCCTG | 55230 |
rs556740059 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | USP40 | GRCh38.p7 | 2:233494943 | ATATATATATATATA[C/T]ATATATATATATTTA | 55230 |
rs556754481 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233549164 | GTAATGGCCTCCGTA[A/G]CAGCCACCTTTGTGT | 55230 |
rs556755323 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233567830 | TAGTTATATAACCTT[A/C]TATAAGATTATAGTT | 55230 |
rs556784198 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | USP40 | GRCh38.p7 | 2:233516333 | TCAATTTCTTTAAAA[A/G]ATGTTAAGATTCTGT | 55230 |
rs556853925 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | USP40 | GRCh38.p7 | 2:233531427 | TTTGTTGGATCTTTG[A/T]TCAATTCCTAAGCTA | 55230 |
rs556867398 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233551755 | CCGGTTTTATCTTTA[A/C]TGTTGATATCCTGAA | 55230 |
rs556927952 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233566922 | GCGGGCAAGGTGAGC[G/T]CGCTTACAAGTCCGC | 55230 |
rs556930629 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | USP40 | GRCh38.p7 | 2:233482599 | TTTTTTTTTTTGTTT[G/T]TTTTTTTTTGACACA | 55230 |
rs556991406 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233480756 | CTGAAGCCACAGCAG[C/T]GTCCCCTGGAGTGGC | 55230 |
rs557009156 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233564166 | CTAGGAAGGTAACAG[C/T]GGTAAATATTTACTA | 55230 |
rs557010889 | snp | C/T | 0.000106992 | 0.00731331 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486020 | ATCCAAACAAACAAA[C/T]AAAACCACGTGGTAA | 55230 |
rs557019774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233506620 | ACAAAGGGAGCTGGG[C/T]GGGGTTGCTCACGCC | 55230 |
rs557068522 | snp | C/T | | | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233566996 | TTCACATTTATAAGA[C/T]TATAGCTATATGATC | 55230 |
rs557080356 | snp | C/G/T | 6.50108e-05 | 0.00570104 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233491239 | GAGGAGAGAAACTTG[C/G/T]GCAGGCTCGTTCCCA | 55230 |
rs557080943 | snp | A/G | 3.5003e-05 | 0.00418333 | intron-variant | USP40 | GRCh38.p7 | 2:233498634 | AGGAGTCAAAATTGG[A/G]ATAAAAAAAATTCAA | 55230 |
rs557140330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233479749 | GCACCAGGACCTGAG[A/G]GCTGCAGAGCTGCGA | 55230 |
rs557161951 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233538607 | CCTTAAAAACCATAA[G/T]TTTCCAAAATAAACA | 55230 |
rs557201552 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233475864 | TAAGAAGGGCTGGGC[A/G]CCCAGCTCGTCACGA | 55230 |
rs557214419 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | USP40 | GRCh38.p7 | 2:233490278 | AAGTGATTCTCCTGC[C/G]TCAGCCTCCGAGTAG | 55230 |
rs557300761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233520826 | GAAATATGCTAAGGG[C/T]TAACATAGGTAAACA | 55230 |
rs557326388 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233488122 | CTCTGTTTCAAGTTG[C/T]TAGGCTACTTAGAAG | 55230 |
rs557364745 | in-del | -/GCGGC | 0.00279162 | 0.0372561 | intron-variant | USP40 | GRCh38.p7 | 2:233477716 | CCCTGCTTTGCACTG[-/GCGGC]GCAGCACGGCATGGT | 55230 |
rs557379598 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP40 | GRCh38.p7 | 2:233557977 | GCCATTGCACTCCAG[A/G]CTGGTGACAGTGAGA | 55230 |
rs557394067 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233558626 | GGGATGGAAAGTTAC[A/T]GCTAACGGGTATGGA | 55230 |
rs557457761 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233566392 | TTTTTCTTTTCCTCA[A/G]AAGAAAACTAAAAAA | 55230 |
rs557517934 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP40 | GRCh38.p7 | 2:233502554 | CCTCCCCAGAGAGAG[C/T]GCTGCACAGCTGCCT | 55230 |
rs557573545 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233545170 | CTACAAAGTCTTCAG[A/C]TGCTGCAATTATCAG | 55230 |
rs557585604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233545630 | AGGGATCATCTTCCA[A/G]GCACACTAAGAGAGA | 55230 |
rs557597051 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233499058 | TGTTACACAGGTAAA[C/T]GTGTGCCATGGTGGT | 55230 |
rs557625634 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233521360 | TCACAGAGAACTTCT[C/G]TAAGTAAACAGTTGC | 55230 |
rs557639786 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476230 | TCTGCCCTCACACTT[C/T]AGTGCTGCTTCCCAT | 55230 |
rs557643834 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233514063 | CCCCAACTTAAAAAG[A/T]GCTTTTAAAATACTG | 55230 |
rs557694047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233512997 | TATTAATATTATACA[C/T]GTATTGGGAAAGGAA | 55230 |
rs557707636 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233532217 | CAACTTCACTCCAGC[A/C]TCTGAATGGGTGTTG | 55230 |
rs557708939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233552214 | TAGTGGGTAAAAAAA[A/G]AAGTTGAATGAAAAA | 55230 |
rs557762162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233530914 | ATCACTTTGCCCTAG[C/T]TTTTTCTTTCTTTGC | 55230 |
rs557793060 | snp | A/C | 0.000152737 | 0.00873756 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233491218 | GATCTCTATGTCTCC[A/C]AAGTAGAGGAGAGAA | 55230 |
rs557793642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233480223 | AAGATACTGAGGGGC[A/G]GAAGAAGGGGATTAG | 55230 |
rs557823391 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233522307 | TCTGTCTTCACTTTT[C/G]TATTTCCCCAGTCCC | 55230 |
rs557855049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233480605 | AAGTGCAGAGCCAGA[C/T]AACGGCAGGCGGCGC | 55230 |
rs557868072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233505745 | TTCTACCAAACATTT[A/G]AAGAATATCAATTCT | 55230 |
rs557870983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233557196 | CACCTATTTTTATTT[A/G]TACTAAAAAATGAAA | 55230 |
rs557886955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233497846 | CAAAGAGCATTCCAG[A/G]GCAAGGCCCCAGCAT | 55230 |
rs557900732 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233557913 | AGCTACCTGGGAGGC[A/C]GAGGCAGCAGGATGC | 55230 |
rs557906966 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233475722 | GACTTGCAGACATTC[C/T]GCGAGGCTTCTGGCC | 55230 |
rs557915659 | snp | A/G | 3.4222e-05 | 0.0041364 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551405 | GCTTGAGATTAATCC[A/G]GAGAGGGAATGTATA | 55230 |
rs557922886 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233528896 | GCCCCAAAAGAGAAT[A/G]CTGAGATCATAAAGT | 55230 |
rs557946366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233490288 | CCTGCCTCAGCCTCC[A/G]AGTAGCTGGGATTAC | 55230 |
rs557984664 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233557087 | CATTAAAAAAACAAA[C/T]ATTAGTCAATAAAAA | 55230 |
rs558069356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233479042 | GTGTTCAGAAGACAC[C/T]AGTGGTCTACTGTTG | 55230 |
rs558104070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233527900 | CTAGAGACCTGCTTA[C/T]ATCATTATGTTAAGT | 55230 |
rs558110386 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475240 | CGATCTTGGCGCACT[A/G]CAACCTCTGCTTCCT | 55230 |
rs558113269 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233485037 | GCATCAGGTTAAGGC[A/G]TTTCCTTCTATTCCT | 55230 |
rs558174407 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233564769 | CCATTAATCAAGCAG[A/C]TTAATATTCCTGTAA | 55230 |
rs558186938 | snp | C/T | 0.000114162 | 0.00755433 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233565483 | CAAAGCTTTAGTCTT[C/T]AATTTCTTCCCTTTT | 55230 |
rs558198316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233557908 | ATCTCAGCTACCTGG[A/G]AGGCCGAGGCAGCAG | 55230 |
rs558216091 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233510518 | AGCGATTCTCCTACC[G/T]CAGCCTCCCATGTAG | 55230 |
rs558332834 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | USP40 | GRCh38.p7 | 2:233555382 | TGTGTGCAACAGCTT[A/T]ATTTTAAGAGATTTT | 55230 |
rs558394969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233479380 | CCATCCTGGCCAACA[C/T]GGTGAAACCTCGTCT | 55230 |
rs558427678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233528405 | GACTCGAAGCCAGTG[C/T]GAAACACAGGTAGGG | 55230 |
rs558440112 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233520591 | AATGTAAAACAATTT[A/C]AGATAAATTTAAAAA | 55230 |
rs558495305 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233495903 | GTGTATGTGCTGATA[C/T]GAGGAGCTCCGCAAG | 55230 |
rs558523719 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | USP40 | GRCh38.p7 | 2:233479334 | CTTTGGGAGGCCAAG[A/G]CGGGCTGATCACAAG | 55230 |
rs558561940 | in-del | -/TTATG | 0.00557542 | 0.0525036 | intron-variant | USP40 | GRCh38.p7 | 2:233527905 | GACCTGCTTACATCA[-/TTATG]TTAAGTAGCAGATTT | 55230 |
rs558564669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233525379 | TAGTTAAGAAAGTAG[C/T]AGGTGGGGAAGGACT | 55230 |
rs558577976 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233561135 | GAATACGCTAAAACA[A/C]CCCAGTAAATCATAG | 55230 |
rs558660323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233553824 | ATGGCAAAAGATATC[A/G]GTTGCTTCAGTCCTG | 55230 |
rs558698341 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233536415 | GAAATTGTCCAAATT[G/T]AAGTAGGAAAAGAAA | 55230 |
rs558715849 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233566837 | CTGGAGCGCCGGCCC[C/T]TCGCACGGGGCCTTA | 55230 |
rs558720798 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477071 | TGCCTCCATACCTGC[A/G]GTTCACGCACACGTT | 55230 |
rs558727974 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233559418 | AAAATTTACTTACAA[C/T]GTAATTGATCCATTA | 55230 |
rs558759778 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233515059 | TGACTTTGAGATGCA[C/T]TCATGTGTTGTATGT | 55230 |
rs558812322 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233532658 | TGCCAAGAACCTGGA[A/C]AACTTGCACTCATGA | 55230 |
rs558915677 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233552782 | TATAGTTTTATCTAT[A/C]ATCTCCAGGATACAA | 55230 |
rs558921862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233515426 | ACTCCACTGGGTGCA[C/T]AGTAGGGTGTCATTT | 55230 |
rs558976955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233503548 | AAGCATTAAGTCACA[C/T]ATAAGGAAATCCCCA | 55230 |
rs558988050 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233534566 | TGGAAAGAAAGTAAT[A/G/T]TGTGGTAATGTCAAC | 55230 |
rs558990113 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233546919 | GTAACAGTAAGGGCC[A/G]AAACACAGTAGATGA | 55230 |
rs559044513 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | USP40 | GRCh38.p7 | 2:233540126 | TGGACCTCAACTCAA[A/G]AAAAAAAAAAAAACA | 55230 |
rs559078842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233559655 | AGTGTCTAAAAATAT[A/G]TATTTCTGGCTTGTA | 55230 |
rs559106864 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP40 | GRCh38.p7 | 2:233532236 | GAATGGGTGTTGCCT[A/G]CAGCCAATCAGACTG | 55230 |
rs559158399 | snp | C/T | 0.000108077 | 0.00735029 | intron-variant | USP40 | GRCh38.p7 | 2:233523138 | AATTAAAATGACTTT[C/T]AGAAATCCTTTTTCT | 55230 |
rs559266605 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233498949 | CAATAAAATTGAAAG[C/G]AATCAGTGGAAGACC | 55230 |
rs559269420 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233528274 | GTGAGCCACTGCGAC[C/T]GGCCCCATGAAATAT | 55230 |
rs559277647 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233490619 | CCAACAGTAGGCGGA[G/T]GCTGCTTCAACACTG | 55230 |
rs559280406 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233507566 | GTTAAGTGAACGAAG[A/C]CAGGCACAGAAAGGC | 55230 |
rs559330750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233508247 | ACTAATGTTCACATT[C/T]CTCTACTTTCTCTTA | 55230 |
rs559394108 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233496888 | GAAAGGAGCAGATCA[C/T]TGATCTTTTTAAAAC | 55230 |
rs559497687 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233500546 | ATTTCTATTACACTA[A/G]AGCAAAAGAGAGCAA | 55230 |
rs559564376 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233559971 | ATTCTTTAAGTGTTG[A/T]CTAAGGCTTTTGAAA | 55230 |
rs559566314 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233493111 | TCAATATTCTGGTAC[A/G]TGGTGATAAATGGGG | 55230 |
rs559616769 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233531040 | TAATTTCATTTAAGT[A/G]ATTTGTATAACAAAG | 55230 |
rs559621031 | snp | C/T | 0.000301176 | 0.0122677 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485832 | TTTCAATCTTCTCCA[C/T]GGGAAGACGATAGAA | 55230 |
rs559662999 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233498038 | AAATATCATGCTATT[A/T]GGACCAACAAGATGA | 55230 |
rs559670628 | snp | A/G | 0.00142052 | 0.0266129 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233488250 | TTACCCCAAGTTTTC[A/G]CCTTTCTGAAGGGGC | 55230 |
rs559705179 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233558084 | GACTTCTATCTTGCC[C/T]TTTAAAATACAAGAC | 55230 |
rs559713330 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233566960 | TTCGCGGGTCCACTC[C/G]GCCAGCGGACCACTC | 55230 |
rs559729975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233488652 | AGGCACAGTGGCTCA[C/T]GCCAGTAACCCAGCA | 55230 |
rs559766841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233545267 | TTAAAAATGACAGGA[A/G]GGAAGAGGCAAACCG | 55230 |
rs559822166 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233480060 | GTCCCCCTTCACACC[A/C]TCCAGCAGCCTCTAA | 55230 |
rs559829233 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233518439 | GGGCGTGGTGGCACA[C/T]GCCTGTAATCCCAGC | 55230 |
rs559845590 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233483416 | GGATCGCTTGAGCCC[A/G]TGAGGCAGAGGTTAC | 55230 |
rs559892129 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233557399 | CACTGAGATCAGAGC[A/T]CATGTGAATAGTCCG | 55230 |
rs560035223 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233537031 | TGGGATTACATGTGC[A/G]CACCACCGCATCCAG | 55230 |
rs560053353 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233501792 | GGGAGAATAAGAAGA[A/G]CTTTACTGTGAATAT | 55230 |
rs560059094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233544753 | TCCCTAAATGGCTAT[A/G]CCTTCAATATAACCA | 55230 |
rs560083297 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233554927 | AAACTCCATTTCTTT[A/T]TTTTCTTTTGCTAGG | 55230 |
rs560091138 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233539697 | AGTATTAGAAGGTTT[-/A]AAAAAAAAAACTGAG | 55230 |
rs560126445 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233520548 | AGTTCCTTTTAAGAA[C/T]ACCTGGCTTTACAGA | 55230 |
rs560175072 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233504244 | AAGGAAGAAAAAGAT[A/C]TACAAAACAACCAGA | 55230 |
rs560206323 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233527260 | CTTAGGAGAGAAGAT[G/T]TGGGTCAACCCTCTA | 55230 |
rs560297677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233547506 | GTATTACAAGTAAAT[A/G]TGGAGCAAGTATTCG | 55230 |
rs560361647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233540483 | ACTTCTTGTTTCTAT[A/G]ATAAATAACTCAGTA | 55230 |
rs560373273 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233502422 | TTACCAGCTAAGTAA[A/C]CTCAATCCAAAAATC | 55230 |
rs560434682 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233494408 | AATAATTTGCCTGTA[A/C]CTGTCATATTTTAAA | 55230 |
rs560457433 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233514268 | GCTACAGTGATAAAT[A/G]CTATGAAGGAAAAGT | 55230 |
rs560467503 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233479810 | CTATCCTGGGGCTCC[C/T]GGGGCCCTTAGGGAG | 55230 |
rs560550840 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233560840 | TCGGTATTGTTGCAA[A/T]AAAAGTGCTTTAAAT | 55230 |
rs560554013 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233541696 | AGGATGAATGAATAA[A/G]TGAAAGAAGACCTCA | 55230 |
rs560567444 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233517350 | AAGAAAAGAAGTCAT[C/T]ATACAAAAAAGATAC | 55230 |
rs560580723 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233545024 | GGCACTTTTAACTCA[A/G]TCCTCAAATTACTCC | 55230 |
rs560623791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233492813 | ATTAAAAATATACTC[A/G]CTCCATTTCTTTATA | 55230 |
rs560647603 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233481584 | ACTTTAAAGGGCTAC[C/T]AGGCAACATGAAGAC | 55230 |
rs560714719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233539451 | TTAGAAATCAATTTA[C/T]TGACATAACAAAAAG | 55230 |
rs560738030 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, missense | USP40 | GRCh38.p7 | 2:233487822 | AGTGGGAGACAGATA[C/G]TAACAAATAAATCAG | 55230 |
rs560756804 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233481070 | GGGCGGAGAAGGACC[C/T]GCCACACTGGTGTGC | 55230 |
rs560771836 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233541371 | GGCATTATCATAAGA[A/C]GACGAAGTTTGGACA | 55230 |
rs560779852 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233533067 | AAATAAAGGAGAAGA[C/T]ATAAAAGAATCAGGA | 55230 |
rs560829181 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233500543 | TTGATTTCTATTACA[C/G]TAGAGCAAAAGAGAG | 55230 |
rs560848771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233548250 | AGTGGTTATTGAGCA[C/T]TGTTTCAAAGAGCAA | 55230 |
rs560879404 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233534203 | TCTGTTGGGATAAGG[C/T]AGTAATTATCAACCT | 55230 |
rs560890435 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233492969 | AGAAGTCAGTGAGAT[G/T]ATATCAAATGCCCTA | 55230 |
rs560906841 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233480940 | GGAGGAAGGAGGGGG[A/C]CCGGGGGGCCATGGA | 55230 |
rs560928176 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233565907 | ATAAGTAACAGCTGT[G/T]TTTAAAAAGGCACGT | 55230 |
rs560966619 | snp | C/G | | | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475181 | TTATGTATTTTTTTT[C/G]AGACGGAGTCTCGCT | 55230 |
rs560972038 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476863 | GGAGCATGCGGGGCC[A/G]GAACGAGTGGGGGAA | 55230 |
rs561014271 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233531651 | TTTTCATTAACAGCA[C/T]AGTTATGTAACTGTT | 55230 |
rs561066477 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233503693 | CTTCAGAAATAAAGG[C/T]GAGATATAAATCTCA | 55230 |
rs561071155 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233554174 | AATAAAGTTTTCCCC[A/G]GAGAAAAGGAAGTTG | 55230 |
rs561081161 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477174 | TGGCAGCTGGGTGGG[C/T]GACATCCAGAGCTGC | 55230 |
rs561136342 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233554864 | AGGTATACAGTACTG[A/T]TTTAGACTAGACTAT | 55230 |
rs561216889 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233509683 | CCATCTCTACTAAAA[A/G]TACAAAAATTAGCTG | 55230 |
rs561372072 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233546802 | GGCGGAGTGAGAAGG[C/G]CACTTTCTTAAGGAT | 55230 |
rs561420723 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233513545 | GTCAAGTGTGTACTT[C/T]ATTCAGTTACAGTTA | 55230 |
rs561449258 | in-del | -/T | 0.00184843 | 0.0303446 | intron-variant | USP40 | GRCh38.p7 | 2:233561113 | CTTCTTTAAAAAAAA[-/T]TTTTCTGAATACGCT | 55230 |
rs561470998 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486240 | GAACTTCCTCAGTGC[A/G]GGAGAAAAGGAAAGA | 55230 |
rs561528587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233550234 | AAAGACAAGGTGTAC[A/G]CAAAGATGCCAAGTG | 55230 |
rs561529272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233479478 | TGAGGCAGGAGAATC[A/G]CTTGAACCCGGGAGG | 55230 |
rs561562535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233536592 | GGAGGCAGAGATTGC[A/G]GTGAGCTGAGATTGT | 55230 |
rs561573681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233538985 | AGTGGGCTGTGACTG[C/T]GCTCCTACGCTTCAG | 55230 |
rs561610750 | snp | C/G/T | 0.000127275 | 0.00797649 | synonymous-codon, missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485887 | GCCGGCAGTCCCACC[C/G/T]TGGGCCGCGTTCCAC | 55230 |
rs561703178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233528779 | ACATAATCAGGCAGT[C/T]TGGTCCACAAGGAGA | 55230 |
rs561718296 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233566304 | TCGAGTGTGGCGGAG[A/G]GTCACTTGGAGATGA | 55230 |
rs561719634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233542930 | ATTTTACATAATTTG[A/G]TATGTTGAGTTTTCA | 55230 |
rs561764219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233520917 | ACTGTTCTGAAAGAT[C/T]AAGGTATTGTTTTCT | 55230 |
rs561783264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233534809 | TTTCTATATAGCCAC[A/G]TTTTTCTTTGTTTGA | 55230 |
rs561817154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233549588 | AGAGAAACCCATCTT[C/T]GTACAATACCTATTT | 55230 |
rs561819140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233488798 | GAGGTCCCAGCTACA[C/T]AGGAGGCTGAGGTGG | 55230 |
rs561824586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233513311 | TTGTTTCTTTGTGTA[C/T]TTTCTTCTCTGTTGG | 55230 |
rs561881692 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233489072 | TCCAACATTTCTGAG[G/T]GAGAAACAGCCACTC | 55230 |
rs561967121 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543582 | AAGATGAGCCCTCAT[C/G]AATGGGAGTAGTGCC | 55230 |
rs561979193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233535572 | CCCTGGAACTAAAGC[C/T]AAAATTGTAACAGAC | 55230 |
rs561986350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233528058 | ATCTTGGCTCACTAC[A/G]ACCTCTACCTCCTAG | 55230 |
rs561987206 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233516596 | GAGAGGCTGAGGCAG[A/G]AGAATGGCGTGAACC | 55230 |
rs562039392 | snp | A/T | 0.0399052 | 0.1355 | intron-variant | USP40 | GRCh38.p7 | 2:233518221 | TATGTTTTTTTTTTT[A/T]AAAGTCAAAACCAAA | 55230 |
rs562048941 | in-del | -/GGA | 0.00537557 | 0.0515644 | intron-variant | USP40 | GRCh38.p7 | 2:233519714 | AAGTTGTAAAAAATG[-/GGA]GGAGATGAAAATGAG | 55230 |
rs562053204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233518746 | CCAGCAATTCCAATC[C/T]GGTACATGTACCCAA | 55230 |
rs562100666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233483472 | CTCCAACCTGGGTGA[C/T]GGAGTGAGACCCCAT | 55230 |
rs562129863 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233549830 | TTAGTGGAAGAGGTT[C/G]TTTCTTGTTTTATTA | 55230 |
rs562136896 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233475700 | GCACAACCCACACGC[A/G]TCTTTGGACTTGCAG | 55230 |
rs562164360 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233483847 | ATAAAATTAATTTTA[C/G]GGTTATGAAAATTAA | 55230 |
rs562190400 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233503302 | TAAATGAACAAGTTT[G/T]CTCATTGTAGAAGTG | 55230 |
rs562224251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233477610 | ATAGGCCACAAGGAC[A/G]TGCATTTGCAATTGC | 55230 |
rs562269053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233482725 | CCACCCAAGAAGCTG[A/G]GTTTTGCCATGTTGC | 55230 |
rs562275563 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233479068 | TGTTGTGCAAACAGC[A/C]CGTGTGAGGCTTAAG | 55230 |
rs562276236 | snp | A/C/G | 0.000113314 | 0.00752625 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562725 | TATAATAATAATAAT[A/C/G]ATAAAAATACCTTTG | 55230 |
rs562290283 | snp | C/G | 0 | 0 | intron-variant | USP40 | GRCh38.p7 | 2:233478045 | GATGTGTGTGGCCCA[C/G]CCACGCTGCACAGTC | 55230 |
rs562398421 | in-del | -/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233540972 | AAACTTGGATTTTTG[-/C]CATTTTCCATGTGCC | 55230 |
rs562400443 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233518985 | ACTAACCTCAAAAAT[G/T]ATATGCTATGTGAAA | 55230 |
rs562447456 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233534658 | GACAACATTGTTAAC[A/G]TTGTGTATGAGAACA | 55230 |
rs562449278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233479872 | AAAGCAGCCCAGACC[C/T]CGGAGAGCAGAGAGG | 55230 |
rs562510328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233527372 | CTGGAGATGGTGCTC[A/G]ATGTCTGAATTAAGA | 55230 |
rs562514201 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233494511 | AAGCCACATATGCAA[G/T]AATATTCTTACAAAT | 55230 |
rs562525365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233527933 | CAGATTTACTTCCAT[A/G]TCATCTATCATCCTT | 55230 |
rs562528695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233548881 | AGAATCTAGGTAAAG[A/G]GTATACAGGAGGTGT | 55230 |
rs562542589 | snp | C/G | 0.000322997 | 0.0127041 | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233561244 | TATGGAACCAAAAAA[C/G]AGCCCGCATCGCCAA | 55230 |
rs562554202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562576 | GTTGTGGGTTGGGGG[A/G]AGGGGGGAGGGATAG | 55230 |
rs562587576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233542182 | ACCTAGCAATTAAAC[C/T]GCATACATTCTTACA | 55230 |
rs562616023 | in-del | -/TGAA | | | intron-variant | USP40 | GRCh38.p7 | 2:233478421 | CTCTTTTATCATGAG[-/TGAA]TGAATGGCTGAGCAT | 55230 |
rs562620652 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233519531 | TTCTCCCTAAACTGT[C/T]TTTTGTATTCTCCTA | 55230 |
rs562621895 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233488327 | TAAGTGAAACAAGAT[A/T]ATATTGAGTGACATA | 55230 |
rs562721269 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233532478 | TGGGAAACTTCTAGG[G/T]GATATTTGGACCGGA | 55230 |
rs562738522 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233481860 | GCAGGTTGTTTTCCA[C/T]ACGCATGTTATTTCC | 55230 |
rs562768699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233542777 | CTTTGAATTCCAGCT[C/T]CTGGTTGAGCAATCC | 55230 |
rs562879098 | snp | A/G | 0.000131411 | 0.00810483 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233491189 | TTCAGCTCCGCCAGC[A/G]TGGCATCTTCTGAGA | 55230 |
rs562904039 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233509965 | AGTTTAGGACCTCCA[A/G]ATCTTAACACAGGAT | 55230 |
rs562939719 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233558299 | AAATTTTCACAGCAT[G/T]AAGAAGAAACCAGCA | 55230 |
rs563012944 | snp | A/C/G | 5.13539e-05 | 0.00506703 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477390 | GCCGTGCAGCGGCGC[A/C/G]GTTATCTGAAGCTCC | 55230 |
rs563029326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233481623 | TCCACATCAGCACAC[A/G]GATCTCTCATCGCCG | 55230 |
rs563076676 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233484144 | GCCTGGGCAACAGAG[C/T]GAGATACTGTCTCAA | 55230 |
rs563082570 | in-del | -/CT | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233498809 | GTCTCATCAAGCTCA[-/CT]GACATGATCTCACCT | 55230 |
rs563176505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233529860 | TCGCCCAGGCTGGAG[C/T]GCAGTGGCGCAATCT | 55230 |
rs563268740 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476269 | GGGCTGACGAGAAAC[C/T]GTGAGGCCCAGGTGA | 55230 |
rs563378731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233498876 | TCATTCATTTTACAT[C/T]CCGTCATCTATACCA | 55230 |
rs563436037 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | USP40 | GRCh38.p7 | 2:233479560 | AGGTGGGACTCCGTC[A/G]CAAAAAAAAAAAAAA | 55230 |
rs563443479 | in-del | -/TG | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233509377 | AAACATTCATACCAC[-/TG]TGTGTGTATATAAAT | 55230 |
rs563478237 | in-del | -/AA | 0.249772 | 0.25 | intron-variant | USP40 | GRCh38.p7 | 2:233533792 | GAACTACACAGAAAC[-/AA]AAAAAAAAATGCTAA | 55230 |
rs563592409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233545228 | AAGGTGCTTGAAGAA[A/G]TTTATGACAACGGGA | 55230 |
rs563610134 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476045 | ACGGAAACGCACAGA[C/T]GTCTATGGCAGACGC | 55230 |
rs563634379 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233504084 | GTTGGATACAGCTTA[A/C]AATAGTCTATTATAA | 55230 |
rs563648307 | snp | A/T | 0.000166481 | 0.0091221 | intron-variant | USP40 | GRCh38.p7 | 2:233496838 | GTGTTGCATCCTGGG[A/T]AGACAAAAATGCTTT | 55230 |
rs563685502 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233551134 | CTGAAGACAGTTTTG[G/T]TTGTCACAACTGAGA | 55230 |
rs563689360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233565116 | TACAGGAATTAAAAA[A/G]GAAATATATTGCTTT | 55230 |
rs563855057 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233484585 | TAGCTCATCCCTAGC[A/G]ATCCTCCTACCTCAG | 55230 |
rs563884248 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233564824 | TGAGATAACTAAAAA[C/T]TGTAAATAGCCTCAC | 55230 |
rs563884496 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233556734 | TTAGAAGAAAAAAAA[A/C]CTCAATAAATTACTT | 55230 |
rs563899633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233493632 | CATAGAAAGAAACAC[C/T]TTGATGACCTAAGAT | 55230 |
rs563915871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233544585 | AACATCAACTCAGGT[C/T]TGGTGGAAAGGGGCC | 55230 |
rs563919527 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233479910 | CCTGGCCCAGGGGCC[A/G]TGCTGCTTGCGGAGC | 55230 |
rs563929732 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476008 | TGCTAGTCAGAGTTG[A/G]GTCCTTAGGGCGCAG | 55230 |
rs563945885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233557315 | ATGGCCATGCCACAG[A/G]AAGCAGAGAGGGATA | 55230 |
rs564103368 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475512 | GTAGCCGGCAACCAA[A/C]AGCAGCTAAGGGCTA | 55230 |
rs564132855 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233553270 | AAATACATTAAAGAA[A/C]AATTCCATAGTGAGA | 55230 |
rs564165491 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233528091 | TCAAGCGATTCTTCT[C/G]CCTCAGCCTCCTGAG | 55230 |
rs564181494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233506153 | AAAAAGTCTGACACA[C/T]AGGCCAAAGCACCAG | 55230 |
rs564290511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233484423 | GATCTTGGACCCTTT[C/T]GAACTCCTCTATCAG | 55230 |
rs564370434 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233511395 | GCAACCTAATCTCAC[A/G]GATGTAAAAATGTGA | 55230 |
rs564373768 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233542134 | ATACAGAGAATGTCC[C/T]TAAGGAAAGACTATG | 55230 |
rs564434067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233479488 | GAATCGCTTGAACCC[A/G]GGAGGCGGAGGTTGA | 55230 |
rs564439709 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233511466 | TTGAAAGTGGTGGCC[A/G]CTCAGCATCAAAGAT | 55230 |
rs564439712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233519452 | TCATTTATAATGTTT[C/T]AAACAAAAACAAACA | 55230 |
rs564456989 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233489687 | CTTCATATTCCTCTG[C/T]ACTGAAATCACCTTG | 55230 |
rs564469417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233503921 | ATCAATCCTCTTCCA[C/T]GAAGGTTTAAAGTCA | 55230 |
rs564512140 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233550340 | TTATTTCAGTTTTGT[A/T]ACATCAAAGTATGTT | 55230 |
rs564604529 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233540606 | GAATTCATGTTGTTG[A/C]GATCATAATGAAATT | 55230 |
rs564612281 | snp | A/G | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486742 | AGAAAGAGAGTTCAC[A/G]GGAAGATGTGGGCCC | 55230 |
rs564647295 | in-del | -/AGT | | | intron-variant | USP40 | GRCh38.p7 | 2:233524680 | AAGGAAAATTTAAAA[-/AGT]AGTAATTATTTTTAT | 55230 |
rs564694469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233478430 | TCATGAGTGAATGGC[C/T]GAGCATATTTTTATA | 55230 |
rs564744111 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233529055 | ACTACATGCCAGTTC[A/G]CTACAACTACTTACC | 55230 |
rs564879642 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486977 | GCCTCCTTGAGAGCA[A/G]GAGTGCCCTGGAAGT | 55230 |
rs564880173 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233497113 | TGAAATTTTAATTAA[C/T]CCTAAAAAGATGGGT | 55230 |
rs564881344 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233565305 | GCATAATTAATTACA[G/T]GTAAAGAAGATGGTA | 55230 |
rs564956914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233548108 | AACTGGCATAGTACA[C/T]TGGTAGAGAAAAATT | 55230 |
rs564959560 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233515792 | AAGATTTCCTCATAT[A/G]TTTTCTCCCAGAAAT | 55230 |
rs565005915 | snp | C/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476536 | TCAGGAAACCGGTCA[C/G]GCTGCCCAGGACACC | 55230 |
rs565067217 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233480845 | GAGGTGGCAGCAAGA[A/C/T]GGGGTGGTTCTGGAG | 55230 |
rs565203854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233560732 | TATCACCACAATAAC[A/G]AACAAAATAATTAAC | 55230 |
rs565249391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233523824 | AAATTCACTCTCTAC[C/T]TCCAAACCACCCCCA | 55230 |
rs565260491 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233538790 | GGGAGGCCAAGGTGG[C/G]AGGATCTCTTGAGCC | 55230 |
rs565339115 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233552595 | TATCTTTCCAACACT[C/G]TTCCAAACTCTGAAG | 55230 |
rs565372320 | snp | A/C | 0.00857473 | 0.0649141 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485660 | TCTTAAATAAGCAAA[A/C]CTCAACCTCAAGTTC | 55230 |
rs565411215 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476443 | CTTTAAGTTGAATAG[A/C]AATCTGGGTTGGATT | 55230 |
rs565426352 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233498807 | AGGTCTCATCAAGCT[C/G]ACTGACATGATCTCA | 55230 |
rs565449876 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233498364 | TCAGAAATGTTCCCA[A/C]TGCACTGTGACTTCC | 55230 |
rs565559202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233490734 | GAATATCTAGTTTAG[C/T]ATCCTAACATAAAAG | 55230 |
rs565574467 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233514517 | GTACGCAGAAAAGCA[C/G]ATCACAAGGTTACAG | 55230 |
rs565619651 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233551242 | GTCTCCCACAACAAA[A/G]AATAGTTTAACTGAA | 55230 |
rs565668358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233551910 | AACCTGGGACCTAGG[A/G]ACCTGTTTTAAAGGA | 55230 |
rs565670857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233538496 | ATGAAAAAGGAATCA[C/T]AAGTTCATATTCTAC | 55230 |
rs565692266 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233566056 | CCTTCAGTACTATAT[A/G]CCAGATTATGACATT | 55230 |
rs565731954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233530807 | GAAATATATGTAAGC[A/G]CACTCTACAGATAGG | 55230 |
rs565752963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233558514 | AAGACTGTTACGAGA[C/T]CACCTATTGGATCAC | 55230 |
rs565774555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233520549 | GTTCCTTTTAAGAAC[A/G]CCTGGCTTTACAGAA | 55230 |
rs565798941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233521228 | CAAGTTCTACTGAGT[C/T]GTCTCTATGATAAGT | 55230 |
rs565819802 | snp | A/G | 4.73855e-05 | 0.00486729 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485964 | CCTGTGTCCTCAGCA[A/G]CACGTCCTGGGGGCT | 55230 |
rs565821267 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233557635 | GAGGAAGAGCAGCTG[G/T]GGGGAGGGCCAGGAG | 55230 |
rs565893534 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233505716 | GCTGAGGACCTAATG[G/T]CTTCACTGCTGAATT | 55230 |
rs565899190 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233488914 | CCTGTCTATTAAGAA[A/G]AGAAAGAAAAGGAAA | 55230 |
rs565918594 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233494601 | CTGGGCTTGGTGGCT[C/T]ACAGCTGTAATCCCA | 55230 |
rs565954324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233479698 | CCCGAAGCAGCCAGC[A/G]CTGCAGCCCCTCTCC | 55230 |
rs565955205 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233497828 | TTACTGACTGCTAAA[C/G]AGCAAAGAGCATTCC | 55230 |
rs565989187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233529063 | CCAGTTCGCTACAAC[C/T]ACTTACCTATGAGGG | 55230 |
rs566041706 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233528193 | CATGTTGACCAGGCT[A/G]GTCTTGAACTCCTGA | 55230 |
rs566095654 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475228 | AGTGCAGTGGCACGA[C/T]CTTGGCGCACTGCAA | 55230 |
rs566182061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233517661 | CAAAGTGCTGGGATT[A/G]CAGGCGTGAGCCACT | 55230 |
rs566203827 | in-del | -/AGG | 0.00318978 | 0.0398085 | intron-variant | USP40 | GRCh38.p7 | 2:233514343 | GTGGTCAGGGATGAA[-/AGG]AGAAGGAACATCTCA | 55230 |
rs566205386 | snp | C/T | 0.000113863 | 0.00754443 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233565431 | CCTGATTTCTGATTC[C/T]GCTTAAATTGGTGAA | 55230 |
rs566266699 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543251 | AAAAATAAATAATCA[A/G]TAAGTGATGGAAAAA | 55230 |
rs566279110 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543893 | TGGGGAGAGAAAGCC[C/T]AGGCCTACCCAAAGG | 55230 |
rs566296716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486623 | CAAGGGGAAATGAAG[A/G]CTGGTTCTTAGGATG | 55230 |
rs566297125 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233495547 | CAGGCATCAGGCACC[A/G]TGCCTAGCCTACCTT | 55230 |
rs566320955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233525335 | ATTTTATTTCTTTTG[A/G]AAAACTTACAGTGTG | 55230 |
rs566328326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233536026 | TTATCAATTTGTAAT[C/T]AAAAAATAAAAATTT | 55230 |
rs566406806 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233487125 | AGGGTCAAAATCATA[A/C]AGAGCTCACACAAAT | 55230 |
rs566407672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233529869 | CTGGAGTGCAGTGGC[A/G]CAATCTTAGCTCACT | 55230 |
rs566418212 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233482234 | AAGTTTTAAAAATTG[C/T]GGGGAGGCTGAGGCT | 55230 |
rs566484680 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233561337 | ACAAGGGTACAGTAA[A/C]CAAAACAGCATGGTA | 55230 |
rs566530228 | snp | C/T | | | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233498594 | CACCAATCCATTTTT[C/T]GTAAATGCCAGGCAT | 55230 |
rs566579160 | in-del | -/CCACAACTAAT | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233565960 | AAAGAAAACCTGTTG[-/CCACAACTAAT]CCACTGCTGGGACGG | 55230 |
rs566609359 | snp | C/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233475675 | CGCGCCTGCTGGACG[C/G]CACTTCAGGGCACAA | 55230 |
rs566664708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233547710 | TGCAAATTCTTTTTT[C/T]GAGAAATATTATAAA | 55230 |
rs566672523 | snp | C/T | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233540693 | TGCTGTTTTCTGTAC[C/T]TCTTGTTCCAAGATA | 55230 |
rs566693986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233481770 | TCCTGCAAGCCTTAA[C/T]TGCAGGGTTTCACAA | 55230 |
rs566704287 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233560254 | TATTTCTCTAAAATA[A/C]CTCTGATACACACAA | 55230 |
rs566801128 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233566789 | CCAGAAAGTGATTTA[C/T]GGATCGTGGACTATG | 55230 |
rs566851588 | snp | C/T | 0.000164834 | 0.00907687 | intron-variant | USP40 | GRCh38.p7 | 2:233499936 | AAGAAAAACAATGTC[C/T]AATGTTAGTTTTCTG | 55230 |
rs566859361 | snp | A/G/T | 0.00113925 | 0.023841 | synonymous-codon, stop-gained, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233519656 | TTATGGCTTTAATTC[A/G/T]AATATCAAACACCAT | 55230 |
rs566864360 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233567687 | CCTTATATAAGATTA[C/T]AGCTATATAACCTTA | 55230 |
rs566909721 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP40 | GRCh38.p7 | 2:233532053 | CGCACACATAGGAAA[C/T]TGGCTGACCCCAACG | 55230 |
rs566931013 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | USP40 | GRCh38.p7 | 2:233548642 | GGAATCTGAACATAA[C/T]TATTAGACAACAGTA | 55230 |
rs566948904 | in-del | -/AACT | 0.00318978 | 0.0398085 | intron-variant | USP40 | GRCh38.p7 | 2:233536002 | CTTATAAATATATAC[-/AACT]AAAATTTATCAATTT | 55230 |
rs566957093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233500690 | AGTTCAAAGAAAAAA[A/G]CAGATTCATATATAT | 55230 |
rs566983977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233525149 | CAAGTCACATAAATA[C/T]GATTCAGATGGTTTG | 55230 |
rs566984781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233554304 | TTCAAGTATATCCTC[A/G]AGACTTTTTCATACA | 55230 |
rs567103588 | snp | C/T | 2.97677e-05 | 0.00385784 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233481261 | CAGTGTCATCTCTGA[C/T]TGTACTGAAATCATC | 55230 |
rs567121413 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233523940 | TTCTTCACACGACGA[C/G]GGCCTAAAAGGACAC | 55230 |
rs567138226 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233498007 | TCTTCTTCTAAGGCT[A/G]CGCATTTGAACTGGG | 55230 |
rs567178033 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP40 | GRCh38.p7 | 2:233507394 | TTAATGGAGCATTAT[C/T]TACAATCGCCAAGAT | 55230 |
rs567184213 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476926 | CGCTTCTGCTCAGCA[C/T]CAGCGCGGTGGCGCA | 55230 |
rs567194421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233559382 | TCAAACACAAAGCAC[A/G]TAACAAACAAAGAAT | 55230 |
rs567201837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233492461 | TTTACTTTTCACGTA[A/G]AAACATACTGATTAA | 55230 |
rs567241511 | snp | C/G | 4.98749e-05 | 0.00499349 | intron-variant | USP40 | GRCh38.p7 | 2:233540651 | CTTCCCAAAACGATG[C/G]CATGTATTACCTTCC | 55230 |
rs567283302 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476503 | TTTCTTTTTCTCAGG[C/T]GTTTTCATTGAGGCT | 55230 |
rs567356294 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233547154 | TCAACATGAGTGTTT[A/G]GCAAGATTATTGGTT | 55230 |
rs567396097 | snp | A/G | 1.89626e-05 | 0.00307911 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477370 | GAGAGTTCATCGGGA[A/G]TAGAGCCGTGCAGCG | 55230 |
rs567400315 | snp | C/T | | | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233567315 | TATATAAGAGTATAG[C/T]TATATTATAGCTATA | 55230 |
rs567403628 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233494280 | AAATTCCATTTTTTT[C/T]TTTCACCTAGCAGAC | 55230 |
rs567418708 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233534395 | TCCCCATCCACTACG[C/T]CCCTATCCTCTCACT | 55230 |
rs567423304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233540055 | ACTGGAGCCTGGGAG[A/G]TGGAGGTTGCAGTGA | 55230 |
rs567463350 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233553703 | GGAAAATAACTATGA[A/C]TTATACTACAGGAAT | 55230 |
rs567580448 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233538984 | CAGTGGGCTGTGACT[C/G]TGCTCCTACGCTTCA | 55230 |
rs567586174 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233515422 | ATTTACTCCACTGGG[G/T]GCACAGTAGGGTGTC | 55230 |
rs567604925 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233480121 | CACGAGGTCACGCTC[A/C]CCTGCCCTGCCACCT | 55230 |
rs567668071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233480469 | GTGAGCTGAGCAGTG[C/T]GAACTGAGCCTCACG | 55230 |
rs567794652 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233553025 | GTGGGAACGTCACCA[C/T]TGCAGATAATAACGA | 55230 |
rs567815682 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233496181 | AGTCTTGGAGTTTGG[G/T]GCCATTTGTTTCTCT | 55230 |
rs567911636 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233505323 | CCCAAAAGAAGCAGA[A/C]GGGAATAATAAAGCT | 55230 |
rs567993279 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233566275 | GGCCTAGGTGACTTC[C/T]CCAAGGTTTCACATC | 55230 |
rs568005417 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233563625 | AATCTCCCAGTACTC[C/T]CAGCTACATTGTAAT | 55230 |
rs568063934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233556322 | ATTAAATGGGCAATA[C/T]GTGTCATTACAAAGA | 55230 |
rs568074302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233511613 | TAAGAAAAAACTTTT[A/G]GAGAAAAACAATATT | 55230 |
rs568226925 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233490606 | TGCTCATTTCAGTCC[A/C]ACAGTAGGCGGATGC | 55230 |
rs568273136 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486702 | CATCAAAAGAGGTCA[C/T]GCAATGAGAAATGAA | 55230 |
rs568274912 | snp | C/T | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233487101 | CACAGCTTACAACCA[C/T]TGTGACAAAGGGTCA | 55230 |
rs568277565 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233510969 | TCCCTCCTATCAGCT[G/T]GTCATGCACTACTAT | 55230 |
rs568291713 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233478703 | GGTGGGCATAAGTCA[A/C]CTAAGCTGTGGTCTA | 55230 |
rs568323028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233518515 | GAGGTTGCAGTGAGC[A/G]GAGATCGTGTCACTG | 55230 |
rs568332744 | snp | G/T | 1.70825e-05 | 0.00292249 | intron-variant | USP40 | GRCh38.p7 | 2:233554535 | AGTCTTCCTGAAATA[G/T]ACATGAATATAATAT | 55230 |
rs568429210 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233484702 | TGTCCAGGCTGGTCT[C/T]GAACTCCTGGGCTCA | 55230 |
rs568434997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233533316 | ATAAAATGACAAATT[A/G]TTAGATTTCATTTGG | 55230 |
rs568442916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | USP40 | GRCh38.p7 | 2:233487936 | GATGGCAGACTGTCC[A/G]AACACACTGACAACA | 55230 |
rs568471301 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233478100 | ACCCGCCATCCCACT[A/G]CTGAGCAGCCTTTCC | 55230 |
rs568527446 | in-del | -/A | 0.259808 | 0.249808 | intron-variant | USP40 | GRCh38.p7 | 2:233533793 | AACTACACAGAAACA[-/A]AAAAAAAAATGCTAA | 55230 |
rs568543116 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233514469 | TTGTGCACTGAGAAA[C/T]GCAGAAAAGTCAGCA | 55230 |
rs568548068 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233494746 | GTGCCTGTAGTCCCA[C/G]CCCAGGAGATCGAGC | 55230 |
rs568612216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233488395 | AAGCTTTTTTCTTAA[A/G]CAAAGAATTGTTTTC | 55230 |
rs568657710 | snp | C/T | 0.00388314 | 0.0438918 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233561268 | TCGCCAAGTCAATCC[C/T]AAGCCAAAAGAACAA | 55230 |
rs568684979 | in-del | -/CT | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233500269 | TTCATAGACATTAAA[-/CT]CTGAATCCTATAAAA | 55230 |
rs568774711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233502025 | TAGAGTCATCAGGTA[C/T]ATCGAATGTTGGTGA | 55230 |
rs568803815 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233481638 | GGATCTCTCATCGCC[A/G]CGCCAGAAGCACAGC | 55230 |
rs568862424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233483050 | TATGCTGGAGAATAA[C/T]CCTCTGCTGTGTTAC | 55230 |
rs568878110 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233511562 | TTTAAACATCTAGAA[C/T]TATAAGGATATATTC | 55230 |
rs568891593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233510936 | TTCCTTTCTAACTCA[A/G]CCTCACTTGTCATGT | 55230 |
rs568893306 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562864 | TTTAAAAAATTGTTT[C/T]AGAAAGCCAAGACCA | 55230 |
rs568926807 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233480691 | CTGTGGCAGCGGAGT[C/T]CTGGCGGCCAGGGGT | 55230 |
rs569010032 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233555912 | GAGGTCAGGAGATCG[A/T]GACCATCCTGGCTAA | 55230 |
rs569013908 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233525989 | GCTGCTTGAAAGGAA[A/T]GTCTCCCATTGCAAA | 55230 |
rs569069628 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233567784 | TATATAACCTTATAT[A/G]AGATTAGTTATATAA | 55230 |
rs569076895 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233517741 | AAATCATGGAACCAA[A/C/T]CCAAATGCCCATCAA | 55230 |
rs569118972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233533178 | TCTGAGCATATGGCA[A/G]TCGCACTCAAGTTTG | 55230 |
rs569154912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233554373 | AAAAGCAGTTATCTG[C/T]CTTTACCTTTGCTGC | 55230 |
rs569197530 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP40 | GRCh38.p7 | 2:233555004 | TGGCCAGCCTGGCCA[A/G]TATGGTGAAACCCTA | 55230 |
rs569246775 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233493204 | TGATATAATAATAAA[A/C]AACAAGATATATAGT | 55230 |
rs569260891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233487283 | AATATGAGAACAAGA[C/T]AATCATCTTTCATTT | 55230 |
rs569277623 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233510968 | TTCCCTCCTATCAGC[C/T]TGTCATGCACTACTA | 55230 |
rs569305448 | snp | A/C | 1.76173e-05 | 0.00296788 | intron-variant | USP40 | GRCh38.p7 | 2:233551367 | ATTTAAAAATAAAAT[A/C]GTTCAAACCTGTTCA | 55230 |
rs569307292 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP40 | GRCh38.p7 | 2:233500972 | GGTAACCAAGGGGGA[C/T]TGTTAATCCCCTAGA | 55230 |
rs569308473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233548452 | TTCAGAAAAAATTCA[A/G]TAATTGTCAGCTATA | 55230 |
rs569309796 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233550870 | AGATGCATAAATTCA[C/T]CATTACATGTAAAAT | 55230 |
rs569321940 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233551760 | TTTATCTTTAATGTT[C/G]ATATCCTGAAATACT | 55230 |
rs569341250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233493811 | ATAAATGAGAAGCAT[A/G]AACAAGAACAATGCA | 55230 |
rs569345029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233540866 | TTATACCTAATTAAA[C/T]ATGCCTAGAACAGCA | 55230 |
rs569362867 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233542113 | ACAAACATCATTAAA[A/G]TATAGATACAGAGAA | 55230 |
rs569380305 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233502713 | AACCATGTCACCTCT[A/G]TCACAAACACCCGTA | 55230 |
rs569393825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233516042 | TATTTTAGGCTTCAC[A/G]GGCCACATGTGATCT | 55230 |
rs569401977 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233505702 | TTCATCAAAGAAAAG[C/G]TGAGGACCTAATGGC | 55230 |
rs569457383 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233568742 | CCCTTCCTGCACGTC[A/T]CTATAAGATGCACTA | 55230 |
rs569534757 | snp | A/T | 0.000248495 | 0.0111439 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556982 | AAAGCGCTGAAGAGG[A/T]TTCGATTCAGTTCCT | 55230 |
rs569572075 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233553870 | ATATTTTGCTTGACT[A/G]TACAGAAAGAAAATC | 55230 |
rs569625888 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233545463 | AGCCTTCTTTGCCCC[A/C]CTTCCTCAAATGTGC | 55230 |
rs569636719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233497716 | TATATTCTTCTGACA[C/T]CCAAATTTTATGTCC | 55230 |
rs569712121 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233490211 | CTCTGTCACCCAGCC[C/T]GAAGTGCAGTGGCGC | 55230 |
rs569761001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233527707 | CAATTTTTCTTCTAT[A/G]TGCCACAATTAGTCA | 55230 |
rs569790195 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233564395 | AGGTGAAGGCAAAGT[A/G]ATGTTCACACTGAGC | 55230 |
rs569827165 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475185 | GTATTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 55230 |
rs569845598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233513555 | TACTTTATTCAGTTA[C/T]AGTTAATATACCATA | 55230 |
rs569861752 | snp | A/G | 2.7712e-05 | 0.00372226 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233512558 | TTTTGAAAGTTATCA[A/G]AAAGATTTACCTGGA | 55230 |
rs569914722 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233495462 | GGGTTTCACCATGTT[G/T]CCAAGGCTGGTCTTG | 55230 |
rs569920717 | snp | C/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233489402 | GTAAAAGCCTGCCTG[C/G]GCGCTTCCTCTCCAC | 55230 |
rs569946930 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233503526 | AATTCTGAAAGCTAC[A/T]AGATAAAAGCATTAA | 55230 |
rs569959925 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233504677 | AATTGTAAATATATA[G/T]GCAAACACCACCAGA | 55230 |
rs570037427 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233484145 | CCTGGGCAACAGAGC[A/G]AGATACTGTCTCAAC | 55230 |
rs570038533 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233483624 | TGTGAGCAGAGGTAA[C/G]TACAGGTTTTATGGG | 55230 |
rs570153299 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233520130 | AAATTTCTGTTTAAA[C/T]GACTTTATTTTAGAT | 55230 |
rs570187513 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | USP40 | GRCh38.p7 | 2:233494961 | ATATATATATTTATA[A/T]ATATATATATATATA | 55230 |
rs570242254 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233549670 | TGATATATATCTAGT[G/T]GAAATTGTCCTCTAT | 55230 |
rs570264293 | in-del | -/ATC | 0.0203154 | 0.0987167 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562725 | ATAATAATAATAATA[-/ATC]ATAAAAATACCTTTG | 55230 |
rs570286304 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233526867 | ATGATTTATATGAAA[G/T]CAGTGTAAGTAAAAT | 55230 |
rs570299503 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543179 | CATGCCATCTTGCAG[A/T]AGTATTTTAAATGGA | 55230 |
rs570441960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233550653 | ATTCTGAATAAACAT[A/G]TAAGAATGATTTGTG | 55230 |
rs570451849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233564349 | AGCTGAGCTACAAAG[C/T]CATGTAGTGCTGGGG | 55230 |
rs570465713 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233497639 | AGTTGGCTTCTGGCT[G/T]AATTCTTTGATGCCA | 55230 |
rs570505013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233542381 | AGGAAGGAAAACAGT[A/G]TGAGTTTCTATCACT | 55230 |
rs570518527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543103 | ACCCCATTTTATGAA[A/G]GTATTGGGGAACATG | 55230 |
rs570559205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233505230 | GCAATAGATGCCTAG[A/G]TCAAAAATGAAGAAA | 55230 |
rs570580353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233534992 | CATAAAGTGAAGATA[C/T]AATACTTCAAAGAAG | 55230 |
rs570590994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233544082 | AACACCAACTACATA[C/T]GGAGTCCCTAGGGTA | 55230 |
rs570648253 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233547112 | TTTGGACAGGTAAAA[A/C]AAAACTGTCTTTTTC | 55230 |
rs570694781 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233556331 | GCAATATGTGTCATT[A/C]CAAAGAACTGAAGGT | 55230 |
rs570696744 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233517647 | CCGCCTCGGCCTCCC[A/C]AAGTGCTGGGATTAC | 55230 |
rs570782035 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233512429 | TTCTGCAATATAAAG[A/G]TAAGATACCTGGAAG | 55230 |
rs570823387 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233527069 | CAGTTCTCAGTTTTA[A/C]ACAACATGCTCATCT | 55230 |
rs570875214 | in-del | -/A | 0.0311206 | 0.120797 | intron-variant | USP40 | GRCh38.p7 | 2:233533793 | ACTACACAGAAACAA[-/A]AAAAAAAAATGCTAA | 55230 |
rs570902759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233478187 | TATCCTGGTAGGCAC[A/G]CGTCCATGTTTTTGA | 55230 |
rs570912164 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233485144 | ATCTCTTGAGTCTGG[C/T]AGGATTATTTCTTAC | 55230 |
rs570914541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233539631 | TAACTATAATCAACA[A/G]TATAATTTGTTGAAT | 55230 |
rs570927124 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233490415 | GACCTCAAGTGATCC[A/G]CCTGCCTCAGACTCC | 55230 |
rs570936569 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233491940 | CATGCCACTAATGCA[C/T]AGCAAGAAATTACAG | 55230 |
rs570942606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233483209 | TAAGAAATCCTTCTT[A/G]CCAGGCATGGTGGCT | 55230 |
rs570942886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233488852 | TTGAGGCTGTAGTTG[A/G]GCCATGATCACGCCA | 55230 |
rs570976190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233531994 | CTAACTTTCCATTCC[C/T]AAGTAACACAAGGAC | 55230 |
rs571009841 | snp | C/G | 9.77374e-05 | 0.00698993 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562809 | AATAGAGCTTCTAAA[C/G]AAAAAGGTAGAATCA | 55230 |
rs571091141 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233481129 | TTCCGGTCCCTCTCA[C/G]TTTCCAAGCAGGAAT | 55230 |
rs571123793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233502628 | TATCCCCCTCCCCAG[A/G]GAGACCAACACACAG | 55230 |
rs571211786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233547050 | TTCCCAAGCCAGAAT[A/G]GGAGTTCCATTCACT | 55230 |
rs571245200 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233523757 | AAGCCAGATTGGCCA[A/G]GGTCAGTTCACAGAG | 55230 |
rs571267094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233480109 | TTCTGCCATGGTCAC[A/G]AGGTCACGCTCACCT | 55230 |
rs571269126 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233563944 | GTCCCTTTGAGGCTA[C/T]GTTTCTACTTCGAGT | 55230 |
rs571289157 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233523565 | CATGGTAAAAGATTA[C/T]TCTTAGAGAACAACC | 55230 |
rs571329361 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233566636 | ACCAACACTGTCCCT[A/G]CGCTTCCCACGTCCC | 55230 |
rs571346225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233480665 | AGTCCTGAGCAGAGG[C/T]AGAAGATGGCCTGTG | 55230 |
rs571347223 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233526298 | CAAAACACACAGACT[A/G]GAGTGTACCTCACAC | 55230 |
rs571353454 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233513983 | CTTGTATTACAGTAA[C/T]ATGAGGCTAGCATAC | 55230 |
rs571361231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233514651 | TCTAATTCACACGTA[C/T]TGACGATGATCAAAT | 55230 |
rs571363821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233552925 | CTCTTGTGGTAGCTG[C/T]TTAAGACAATGTTCA | 55230 |
rs571422879 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233515261 | TACCTAGACGTAGAA[A/T]TGGTAAGTGGATGTT | 55230 |
rs571429347 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233545676 | TAACCCAGAGAAAAT[A/T]ACACGAGATTGGTCC | 55230 |
rs571453639 | snp | C/T | 1.7321e-05 | 0.00294282 | intron-variant | USP40 | GRCh38.p7 | 2:233498533 | CGAAAGTACAATGTA[C/T]AGAAATCATCTTACT | 55230 |
rs571477716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233484245 | TATTTAATCTAATCT[A/G]TATGGATTTTCATTG | 55230 |
rs571478924 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233546411 | AACAGATATTTTATG[C/G]ATCAAAAAACTGAGG | 55230 |
rs571513214 | snp | A/G | 2.1704e-05 | 0.00329416 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233491220 | TCTCTATGTCTCCCA[A/G]GTAGAGGAGAGAAAC | 55230 |
rs571531926 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233530454 | TAAACATCTTTGAGC[A/G]TCAACATTCATATAC | 55230 |
rs571575837 | in-del | -/ATGGAACCA | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233517731 | TGCAATTGCAAAATC[-/ATGGAACCA]ACCCAAATGCCCATC | 55230 |
rs571590888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233484718 | GAACTCCTGGGCTCA[A/G]GTGATCCACCCATCT | 55230 |
rs571630919 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233565598 | AGTGACATATAAATG[C/T]TTTTATTTTTAAAAT | 55230 |
rs571653258 | snp | C/T | 5.14725e-05 | 0.00507283 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485528 | TGCTGTTAAACAACT[C/T]ACCTTAACACCAATA | 55230 |
rs571654907 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP40 | GRCh38.p7 | 2:233479707 | GCCAGCGCTGCAGCC[C/T]CTCTCCCATATCCCA | 55230 |
rs571762903 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233501587 | ACAGGGTGGTAGTAA[C/T]GAACAGAATGAGATG | 55230 |
rs571770926 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233535328 | CTACCAAATTAGAAA[A/G]AGATAGCAAACTTTT | 55230 |
rs571772794 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233540183 | AACCCCCAAGCAACA[C/G]TGATGAAAAAAGGTG | 55230 |
rs571803004 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233516353 | TAAGATTCTGTGTAA[C/G]AATATATTAAATCTA | 55230 |
rs571809076 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233565807 | CTTATGTGTAAAATA[C/G]GATACCATCTGTCTC | 55230 |
rs571827845 | in-del | -/T | 0.000673674 | 0.0183408 | frameshift-variant, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551418 | CGGAGAGGGAATGTA[-/T]TAACAGCTAGTTTCC | 55230 |
rs571840835 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233518731 | AAATTTGCAAATGAC[C/G]CAGCAATTCCAATCC | 55230 |
rs571852785 | snp | A/C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233475947 | CGCAGTCTACACCCA[A/C/G]TGCGAGTCTCCTGAG | 55230 |
rs571859360 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233544936 | GCTCTAAAACCATCA[A/G]TTTGATGTTGTTAAG | 55230 |
rs571865089 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233550932 | TGGTGAGTTTTCTAA[A/T]TGCAGGGTAAACTTC | 55230 |
rs571873851 | snp | A/G/T | 0.00199529 | 0.0315338 | intron-variant | USP40 | GRCh38.p7 | 2:233537345 | CCATAGATATGGAAG[A/G/T]ATATAGTTAGACTCC | 55230 |
rs571899432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233529187 | TCTCTACTCTTGTTA[A/G]GCTTCGATCCCTACT | 55230 |
rs571922828 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233544426 | TAAATAAATCACTCG[A/T]CACTGGTGACTGAAC | 55230 |
rs571936066 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233537708 | AACTTATAATTCTGT[A/T]TCTATCAAAAATATC | 55230 |
rs571936900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233538243 | AGAATAGAGGAGAAA[C/T]AGAAAACAAATAGCA | 55230 |
rs571946615 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233529670 | ATCTCAGTTTTCCCA[G/T]CTGAAAAATGAAAAA | 55230 |
rs571974400 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP40 | GRCh38.p7 | 2:233479480 | AGGCAGGAGAATCGC[C/T]TGAACCCGGGAGGCG | 55230 |
rs571996979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233528801 | ACAAGGAGATCACGG[C/T]AACATCCATTTTCCT | 55230 |
rs572036983 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233484934 | AGAAGGGGCGGTTAG[C/G]GGAATCCTTACTTTG | 55230 |
rs572063854 | in-del | -/T | 0.000106536 | 0.00729771 | frameshift-variant, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485590 | TTGCAAATAATCTTG[-/T]TTTTTTTTTCTTTTT | 55230 |
rs572078946 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233483891 | CCTACATAGATAACT[A/C]ATTTTCCAGCACCAT | 55230 |
rs572083731 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233519378 | TCAGATATACTCATT[G/T]TATCTGGGGAAGGAG | 55230 |
rs572136980 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233521561 | TATATTGTATACTGC[A/C]TTTCTACATAGAGTT | 55230 |
rs572169393 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233512804 | CAAACCAAAAACCCC[A/C]CAACAACCAAAGAAA | 55230 |
rs572308333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233484375 | TAACACTGCTAAGTA[C/T]GTTTTTGTATATTCT | 55230 |
rs572360792 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233489827 | AGGGCAGAGCCCGCT[C/G]TAACAGTACAACAAG | 55230 |
rs572367373 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP40 | GRCh38.p7 | 2:233527798 | CTGTTTTAACATAGG[C/T]TGCAATGTTAACTCC | 55230 |
rs572367418 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233518783 | TGAAAACATATCTCC[A/T]CACCAAGACTTATGT | 55230 |
rs572461079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233504849 | AAACTTCACCATAGA[C/T]CAAACGGAGCTAACA | 55230 |
rs572478098 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233556527 | ATTACCTCCCTAATT[A/G]ACTTTCTTTACAATA | 55230 |
rs572482668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233516479 | TAGGCGGGCGGATCA[C/T]GAGGTCAGCAGATCA | 55230 |
rs572564263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233509525 | TATTGATAGAAAGAA[A/G]AAAATTGTAATCTTA | 55230 |
rs572589897 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233534456 | TCTTTTCTCTCAGCC[A/T]AATTTACTTTATATA | 55230 |
rs572594436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233496676 | CTGAATTTCCCCATT[C/T]TCCCTAAATGAGGCT | 55230 |
rs572807238 | snp | C/T | | | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233491211 | CTTCTGAGATCTCTA[C/T]GTCTCCCAAGTAGAG | 55230 |
rs572829233 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | USP40 | GRCh38.p7 | 2:233554042 | AGCCATCTACTTTCA[G/T]AGTAGTAAAGAAAGC | 55230 |
rs572869979 | snp | A/T | 0.000616903 | 0.017552 | intron-variant | USP40 | GRCh38.p7 | 2:233561113 | CCTTCTTTAAAAAAA[A/T]TTTTCTGAATACGCT | 55230 |
rs572872411 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233534937 | GATAAACTCTAGGCA[A/G]AAAAGGAAAACAACT | 55230 |
rs572874638 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP40 | GRCh38.p7 | 2:233492816 | AAAAATATACTCGCT[C/T]CATTTCTTTATAATG | 55230 |
rs572878202 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562459 | TCTCAGTAAACTATC[C/G]CAAGAACAAAAAACC | 55230 |
rs572918286 | snp | A/C/T | 1.71176e-05 | 0.00292549 | synonymous-codon, missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477485 | GATGTAGCTGCTCTG[A/C/T]TCATGGAGGGCTTCT | 55230 |
rs572936667 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233491381 | CACTCAAGAGCCTCT[C/G]CATCCAAGTCTTATG | 55230 |
rs572994841 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233499924 | TTAAACACTGTAAAG[A/C]AAAACAATGTCCAAT | 55230 |
rs572995567 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233532222 | TCACTCCAGCCTCTG[A/C]ATGGGTGTTGCCTGC | 55230 |
rs572999089 | snp | C/T | 9.57002e-05 | 0.00691671 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485840 | TTCTCCACGGGAAGA[C/T]GATAGAAATCGGCAA | 55230 |
rs573011310 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486155 | TTCAATTTCCTTTAA[A/T]CTTGGAATGAAGAGC | 55230 |
rs573029681 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476518 | TGTTTTCATTGAGGC[C/T]ACTCAGGAAACCGGT | 55230 |
rs573031821 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233502876 | TCCATCTATAGGAAA[A/C]AGCTCCTCCCTACAA | 55230 |
rs573037033 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476750 | CCTTGCTTAGCAGAG[C/T]GACTCACCCTCGGAG | 55230 |
rs573056937 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233524109 | TCTAATTGCCCTCAC[A/G]TAGGCTGAATAAAAT | 55230 |
rs573060629 | in-del | -/TGTCG | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233482129 | CCTCTGCTAGGAACA[-/TGTCG]TGTCAAGTATTATAA | 55230 |
rs573087694 | in-del | -/AG | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233564494 | TATATAGAGAGAAAC[-/AG]GGGCAAGAAATCAAG | 55230 |
rs573133973 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477053 | GGAGCAACGGCATGC[C/T]GCTGCCTCCATACCT | 55230 |
rs573142335 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233553123 | AGGCCACAGGAAATG[G/T]TATTAATATACATAC | 55230 |
rs573226339 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233545886 | AAAGAGACAAGCACA[A/G]TGTCCACCAGATATA | 55230 |
rs573234133 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233498868 | TATTTTTTTCATTCA[C/T]TTTACATTCCGTCAT | 55230 |
rs573287695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233546692 | ATAATAAACACTTAC[C/T]AGACATGGACAAGCT | 55230 |
rs573340286 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476225 | TCCTTTCTGCCCTCA[C/G]ACTTCAGTGCTGCTT | 55230 |
rs573405372 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP40 | GRCh38.p7 | 2:233539226 | GCAAAAAAAAAAATA[A/G]GAAGAATAGAGAAGA | 55230 |
rs573420464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233506805 | GATCCCAGCTACTTC[A/G]GAGGCTGAGATGGAA | 55230 |
rs573455869 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | USP40 | GRCh38.p7 | 2:233559684 | TAATTTTTTAATGTG[-/A]GAAGGAAACATTCAA | 55230 |
rs573483353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233498737 | ATAATAAAGCTATGG[A/G]CCTCCATGTTAATGA | 55230 |
rs573495907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233552588 | GTGTAGGTATCTTTC[C/T]AACACTGTTCCAAAC | 55230 |
rs573516472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233514884 | TTTGCATCATCCCCC[C/T]TAAAACTCCCTGTCA | 55230 |
rs573517042 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233564214 | AGTCTTTCTAAGCTT[A/G]GAAGCAACAGAAGAA | 55230 |
rs573523486 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233566927 | CAAGGTGAGCTCGCT[C/T]ACAAGTCCGCTGGTG | 55230 |
rs573558710 | snp | A/G | | | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475288 | CTGCCTCAGCCTCCC[A/G]AGTGGCTGGGACTAC | 55230 |
rs573571433 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233531465 | AACTGTCATTTACAT[A/G]TTCCAATTACGTACA | 55230 |
rs573604024 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233515675 | TTTTTGAAGAGTAGA[A/C]GTTTAAAATTTTAAT | 55230 |
rs573608000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233507644 | AAAAAGAGTTGACAT[C/T]GTAGAAGCAGAGAGT | 55230 |
rs573635891 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233503018 | ACAGTAAGTCTCCAG[C/T]AACAAACCCCGAAGA | 55230 |
rs573641423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233516338 | TTCTTTAAAAAATGT[C/T]AAGATTCTGTGTAAG | 55230 |
rs573659973 | snp | G/T | 0.0130921 | 0.0798413 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233567838 | TAACCTTATATAAGA[G/T]TATAGTTATATAACC | 55230 |
rs573694647 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233508413 | GTTTTCTGATCTACA[G/T]TTGGCTAATTGCAGA | 55230 |
rs573723263 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233560470 | GAGAATAAGCATTTA[G/T]AAATTGTAATGGCAA | 55230 |
rs573767645 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233537038 | ACATGTGCGCACCAC[C/T]GCATCCAGCTAATTT | 55230 |
rs573791820 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233531245 | CTTTTTGCATTACCA[C/G]TACACTGTCTTCATT | 55230 |
rs573796148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233499530 | GTATATACCCAGTAA[C/T]GGGATTGCTGGATCA | 55230 |
rs573846886 | snp | G/T | 0.00279162 | 0.0372561 | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475404 | CCTGACCTCAAATGA[G/T]CCACCCGCCTTGGCC | 55230 |
rs573848813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233479836 | GGGAGTCAGCAAAGG[C/T]CACGGGACAGTGCTG | 55230 |
rs573853046 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233492891 | GTGACTTCTGCCCAT[C/T]GTGATGTGTGCGGCT | 55230 |
rs573891096 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | USP40 | GRCh38.p7 | 2:233536877 | TTATATTGTATTAGG[-/T]TTTTTTGTTTCCTTT | 55230 |
rs573916773 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233528383 | TCTTCTCTGAATCCA[C/T]TTGGCTGACTCGAAG | 55230 |
rs573960577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233480266 | CAGATCAGGCTCCTA[C/T]AGTCATTTGGGCAGG | 55230 |
rs573974574 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233499072 | ACGTGTGCCATGGTG[C/G]TTTGCTGCACCTATC | 55230 |
rs574040548 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233558632 | GAAAGTTACTGCTAA[C/T]GGGTATGGAGTTTCT | 55230 |
rs574084392 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233545733 | CTACTAAAGAACTCC[A/C]TGTATGCAGGGCACA | 55230 |
rs574122734 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233494389 | TGCTGAGAAGTTTCT[C/G]TAGAATAATTTGCCT | 55230 |
rs574147069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233564867 | TCTGAAGCCAAACAA[A/G]CTCAGGTGAGATCAG | 55230 |
rs574205882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233514131 | TTACTGTGTATTGGC[C/T]ACGTGCCAGGCACTG | 55230 |
rs574363262 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233542070 | TTCTACCATGAATAT[A/G]TATTTCATTCATAAC | 55230 |
rs574428264 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233557998 | GACAGTGAGACCTCA[C/T]CTCAAAAAAAAAAAA | 55230 |
rs574493121 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233536997 | TTAAGCAATCCTCCA[A/C]CCCAGCTTCCCAAAT | 55230 |
rs574512881 | snp | A/G | 0.000266365 | 0.0115374 | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233561169 | TAATACCTTTGCATC[A/G]GGTTTATCCTTATCT | 55230 |
rs574565809 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233479697 | CCCCGAAGCAGCCAG[C/T]GCTGCAGCCCCTCTC | 55230 |
rs574584129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233509707 | TTAGCTGGGTGTGGT[A/G]GTAGGTAACTGTAAT | 55230 |
rs574626413 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233510651 | TCAGGTGATCCACCC[A/G]CCTCAGCCTCCCAAA | 55230 |
rs574631582 | snp | A/C/G | 6.74313e-05 | 0.00580618 | missense, stop-gained, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477439 | AAGTTTCCGGGGCTC[A/C/G]GGGCCGGGCAGGCGT | 55230 |
rs574645994 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233553956 | GGAGGTAAGGCTATA[C/T]TGGATTTGCCAGAGT | 55230 |
rs574655727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562286 | TTTATTGTGGCATTA[C/T]TCACAATAGCAAAGA | 55230 |
rs574660481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233544722 | CACAATGACAAAATC[C/T]GGCAAAAAGTTGGAA | 55230 |
rs574711710 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233481515 | TTAATTTCCAGCCAT[C/G]TGACCTTTCCCTTCA | 55230 |
rs574730567 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233532344 | AACCAATCAGATGTT[C/T]GCACATGATAGTGAC | 55230 |
rs574739025 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233487469 | TCCAGGAAACTATTT[A/C]TGGTTGTACAACTTG | 55230 |
rs574765850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233541002 | CATCTTCCATTTGAA[A/G]AGCAATATCAAAAGT | 55230 |
rs574777980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233532840 | TAGCTACTAAGGGAA[A/G]AGAATCACTTGAGCC | 55230 |
rs574820169 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233507710 | AAGGGGAGGATGGGA[A/G]AGGGTGGTCAACAGG | 55230 |
rs574833944 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233481397 | ATATTGACAAAAGAA[A/C]AGATTCAAATTTACA | 55230 |
rs574923668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233510534 | CAGCCTCCCATGTAG[C/T]TGGGATTCCAGGTGC | 55230 |
rs575112756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233500410 | TGTGATGTCATGGCA[C/T]AATGCAAAAATGAGA | 55230 |
rs575149534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233508668 | GTAAAATTCTAAAAT[A/G]CCTTCATTTATTAGT | 55230 |
rs575174567 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233492784 | AAGAAAAACATAGCT[A/G]AAGAGTTGGGCCTAT | 55230 |
rs575177616 | snp | C/T | 3.37268e-05 | 0.00410637 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477427 | GGATGGAGAGAGAAG[C/T]TTCCGGGGCTCGGGG | 55230 |
rs575185312 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233509578 | GAGTGGAATGGCTCA[C/T]GCCTGTAATCCCAGC | 55230 |
rs575212982 | in-del | -/TTGAAAGGAACACCCTAAC | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233531965 | CTTCCTAGAACTAAA[-/TTGAAAGGAACACCCTAAC]TTTCCATTCCTAAGT | 55230 |
rs575268337 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP40 | GRCh38.p7 | 2:233554734 | TTAGCTTAAAATCTA[C/T]CAGAAAAATATAAGA | 55230 |
rs575268660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233561444 | CTGATCTTTGACAAA[C/T]CTGAGAAAAACAAGC | 55230 |
rs575302499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233494178 | TTCAAGAAATGTGCA[C/T]TAGAATATTTTTCTG | 55230 |
rs575327136 | in-del | -/T | 0.0260105 | 0.111035 | intron-variant | USP40 | GRCh38.p7 | 2:233482596 | AGTTTTTTTTTTTTG[-/T]TTTTTTTTTTTTGAC | 55230 |
rs575332172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233480852 | CAGCAAGACGGGGTG[C/G]TTCTGGAGACCTGAG | 55230 |
rs575344669 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233481435 | GGTGAATAACTGATT[A/T]AAAAAAATCCTCTTG | 55230 |
rs575346990 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233503619 | CAGAAGAAAATGGGG[G/T]TAATATAGGAAAGAA | 55230 |
rs575361820 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233479350 | CGGGCTGATCACAAG[A/G]TCAAGAGATTGAGAC | 55230 |
rs575394571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233559457 | CAAAGACTAAAAAAC[C/T]GATCAACAGTTTCCT | 55230 |
rs575395045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233516564 | CTGGTGGCGGGCACC[C/T]GTAGTCCCAGCTACT | 55230 |
rs575591842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233560754 | ATAATTAACTCATTA[C/T]TCAATTTATTTCCAG | 55230 |
rs575593548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233547378 | TGTATCTCTCAATAC[A/G]TTCCAAATACAACTG | 55230 |
rs575628304 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233492661 | ATAAGGAGATAAGAA[C/T]TTGACTCATTTATAT | 55230 |
rs575688956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486703 | ATCAAAAGAGGTCAC[A/G]CAATGAGAAATGAAA | 55230 |
rs575716552 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233540132 | TCAACTCAAAAAAAA[A/C]AAAAAAACAAAAAAC | 55230 |
rs575716628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233531674 | TAACTGTTTTAGATC[C/T]GGAAAGTTAATTTCC | 55230 |
rs575775287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233515532 | TGTAAAGTGTCTGTT[C/T]AAGATTCTAAACCTG | 55230 |
rs575777056 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP40 | GRCh38.p7 | 2:233532256 | CAATCAGACTGATTG[C/T]CAGCTATGTCTTCGT | 55230 |
rs575865476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233504450 | AGGGATGGAAAAAGA[C/T]AGTCCATGCAAATAG | 55230 |
rs575875795 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233522790 | AGAAACAATTTAGCC[A/G]TAATGTTAATACCTT | 55230 |
rs575885559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233546789 | AAGGGGAGTTTAAGG[C/T]GGAGTGAGAAGGCCA | 55230 |
rs575947291 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233544307 | TCCGTGGAGTCGCGG[G/T]GGCCACCCTCCCAGC | 55230 |
rs575956747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233483853 | TTAATTTTAGGGTTA[C/T]GAAAATTAATGAATA | 55230 |
rs575960323 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233536753 | CTGCAGTTTCCAAAT[C/G]CACAGATTCAACCAA | 55230 |
rs576011118 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233516120 | CCATTCTTTGCCCAC[C/T]GGCTGAAAAAAAACA | 55230 |
rs576012381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233527180 | CTCAAATAAAATGTA[C/T]CAGGCCTGATTGTCT | 55230 |
rs576033073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233484338 | TCCAAGAACATGACG[C/T]GGCTCTAACAGAAGC | 55230 |
rs576062508 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233536180 | TACTATAATAGCAAA[C/T]AGCTATTATAAATAT | 55230 |
rs576105282 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP40 | GRCh38.p7 | 2:233535537 | TAAGAGGAAGGACCA[C/T]GACCCAGGGCTAAGC | 55230 |
rs576149159 | in-del | -/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233495406 | TTATCTCTCTTCTTG[-/T]TTTTTTTTTTTACTT | 55230 |
rs576174652 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233556032 | AAGGCAGGAGAATGG[A/C]GTGAACCCGGGAGGT | 55230 |
rs576206673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233550128 | GTACATATGGTGGCC[A/G]CTTGATGGGTGTCAG | 55230 |
rs576247048 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP40 | GRCh38.p7 | 2:233483572 | AATGAGTGGTTTTCA[C/T]ATTTAAGTCTTCAAC | 55230 |
rs576320816 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543525 | AACCGCCAATGCAAT[A/G]GTATTAAGAGGTGGG | 55230 |
rs576334210 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233503844 | TATAAAACTCACAAG[C/T]ATAGGTAAATTCATA | 55230 |
rs576352178 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233508526 | GGTCCAGTTGTTTGG[-/T]TTTTTGCAATAAGGG | 55230 |
rs576397400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233496430 | AAAATGTTAAAAACA[C/T]GGTAAGTTTCCAACA | 55230 |
rs576407648 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233497315 | CCACAGGACATGGAA[C/T]AGAAATAAAGGAGCC | 55230 |
rs576436094 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233511125 | AATATCCTTATGATT[G/T]CTGCACTGTAATAAG | 55230 |
rs576462926 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233488655 | CACAGTGGCTCACGC[C/T]AGTAACCCAGCACTT | 55230 |
rs576476551 | snp | C/T | 0.000465076 | 0.0152421 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233511792 | TCAAAGTATAGCTGT[C/T]CGGCACTTAAAAAAA | 55230 |
rs576520384 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233551978 | TTTCTGAGGAGAAGA[C/T]TCATAGCTTTCATGA | 55230 |
rs576546296 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233488089 | TGCCCAGACATACAA[A/C]CATATTTCTAGCACA | 55230 |
rs576568176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233542425 | GTAACAAAATAGGAA[C/T]GTTGGCCAGGCACAG | 55230 |
rs576579139 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP40 | GRCh38.p7 | 2:233541931 | CCAATTCCAATATAC[A/G]TATATAAACATAAAG | 55230 |
rs576590729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562989 | GTGACTCTAAGAAAA[C/T]AGTGTCATGCTAAGG | 55230 |
rs576593620 | snp | C/T | 8.76924e-05 | 0.00662106 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233519655 | TTTATGGCTTTAATT[C/T]GAATATCAAACACCA | 55230 |
rs576659560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233488495 | TTTAGATACTTGAGT[C/T]ATTTCTTACTAAACA | 55230 |
rs576730667 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233540854 | AGACCAACAGGATTA[C/T]ACCTAATTAAATATG | 55230 |
rs576786717 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233554961 | GCCTTAAGATATACT[A/G]AAGAAGTTATAAGAA | 55230 |
rs576903817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233542671 | TGACACAGAGCAAGA[C/T]GTTGTCAAAAAAAAA | 55230 |
rs576974088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562460 | CTCAGTAAACTATCG[C/T]AAGAACAAAAAACCA | 55230 |
rs576991833 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233555977 | AAAAATTAGCCAGGC[A/G]TGGTGGCGGGCACCT | 55230 |
rs577010157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233502442 | ATCCAAAAATCTAAA[C/T]ATGAAATGCTCCAAT | 55230 |
rs577051808 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233515122 | CGAACAGTATCCATT[A/G]CTTAAATACACCATC | 55230 |
rs577055617 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233479281 | TTTAAATGTGGAAAC[A/G]GAGCCAGGCGCGGTG | 55230 |
rs577095826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233510696 | GATGTGAGCCACCGC[A/G]CCCGGCCAACATACA | 55230 |
rs577103319 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233549448 | AATTCTGCCTCTTAG[A/T]TGACCATGAACACAA | 55230 |
rs577133067 | snp | A/G | 1.69278e-05 | 0.00290923 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477466 | GCGTCTCTGCACTGG[A/G]GAGGATGTAGCTGCT | 55230 |
rs577155531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233511062 | TTGGGAACCATGGGC[A/G]ACCTGATTTGAGTCC | 55230 |
rs577162597 | snp | C/T | 0.000399281 | 0.0141238 | splice-donor-variant | USP40 | GRCh38.p7 | 2:233533478 | ATTTTTCTTTCCATA[C/T]CTTCAGGGGGTCTCT | 55230 |
rs577172751 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233526337 | TGAATAAGATCCTTT[A/C]CATTTAAAATATCCC | 55230 |
rs577201695 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233479830 | CCCTTAGGGAGTCAG[C/T]AAAGGCCACGGGACA | 55230 |
rs577201902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233530935 | CTTTCTTTGCTTTTA[C/T]GCTTAGAAAGGTTTT | 55230 |
rs577281541 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP40 | GRCh38.p7 | 2:233482592 | CTGGAGTTTTTTTTT[G/T]TTGTTTTTTTTTTTT | 55230 |
rs577331513 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233516545 | CACTAAAAATTAGCC[A/G]GGCCTGGTGGCGGGC | 55230 |
rs577365835 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233566859 | GGGGCCTTATGGGAA[A/C]TGTAACTCTTCTGCT | 55230 |
rs577372567 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP40 | GRCh38.p7 | 2:233519038 | ATGTTTTATGATTCC[A/G]ATTACATTAAACATT | 55230 |
rs577404037 | snp | A/C | 3.40512e-05 | 0.00412607 | intron-variant | USP40 | GRCh38.p7 | 2:233493387 | AATTTACTTCTCTTT[A/C]TGATGCACTGGCTGC | 55230 |
rs577423462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233537906 | ATACGAAACACTATT[C/T]TTTCCTTAATTTCTT | 55230 |
rs577495354 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233532978 | CTTATTGAGAAACAG[G/T]AAAATAAAGGAGAAG | 55230 |
rs577539192 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476036 | CAGTGCTTCACGGAA[A/G]CGCACAGACGTCTAT | 55230 |
rs577619542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233481950 | CAGGAAAGACACAGC[A/G]CAGGGTCTGCGGGGT | 55230 |
rs577650588 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476261 | CAGTGACGGGGCTGA[C/T]GAGAAACCGTGAGGC | 55230 |
rs577712579 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476656 | GCAGCTGCAGTCCTC[A/G]GGATCCAAGGACCTT | 55230 |
rs577715018 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233559001 | CATTAAAGGCAATAT[A/G]ACAGTATTCCTATCG | 55230 |
rs577747385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233544694 | ATGACCAAATATATA[C/T]TTCTTAATATATCAC | 55230 |
rs577760468 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233545203 | AGAAAATAATAAAAT[A/T]AGTATGTTTAAGGTG | 55230 |
rs577840658 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | USP40 | GRCh38.p7 | 2:233529789 | AACACCCAGATTTTC[A/T]TCTTTTTTTTTTCTT | 55230 |
rs577864684 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233530806 | TGAAATATATGTAAG[C/T]GCACTCTACAGATAG | 55230 |
rs577928457 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233557130 | CAAGCAATCTGAAGA[G/T]CAGATATAAGAATGA | 55230 |
rs577960401 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233530675 | ATGTTCATCTCATTG[C/G]CATTCTTCTTCTTCT | 55230 |
rs577989438 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233551034 | TATACTTTGGAAATT[C/G]AAAATGACTCTAAAT | 55230 |
rs578007605 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233479911 | CTGGCCCAGGGGCCG[C/T]GCTGCTTGCGGAGCT | 55230 |
rs578015471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233497443 | TAGGTGAGAGGCATA[C/T]GAAGGCTTGGACCTG | 55230 |
rs578048377 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233497851 | AGCATTCCAGGGCAA[C/G]GCCCCAGCATACCTC | 55230 |
rs578064264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP40 | GRCh38.p7 | 2:233489893 | TCCTCCACCAGTGTC[C/T]GCTCTGCCGATGAAT | 55230 |
rs578088063 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233557941 | TGCCTTGAACCCAGG[C/G]CTGCAGTGAGCTATG | 55230 |
rs578118141 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP40 | GRCh38.p7 | 2:233527902 | AGAGACCTGCTTACA[A/T]CATTATGTTAAGTAG | 55230 |
rs578180308 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233496036 | AATGTTTTTCTTAGA[A/C]GGATACAGGAGGAAA | 55230 |
rs745364341 | snp | C/G | 4.41258e-05 | 0.00469691 | intron-variant | USP40 | GRCh38.p7 | 2:233511844 | TATTAATTCCTAGCT[C/G]TCTAAGAAAAATAAA | 55230 |
rs745378608 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233555529 | TAATGGCCTTACATA[C/T]GTTGTTTTGAAAATA | 55230 |
rs745422760 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233558411 | GGCATATCCATCTAA[C/T]AGAATCTCATTTGGC | 55230 |
rs745491467 | snp | A/T | 1.96887e-05 | 0.00313751 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477361 | CATCAGCCGGAGAGT[A/T]CATCGGGAGTAGAGC | 55230 |
rs745534260 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233496893 | GAGCAGATCATTGAT[C/T]TTTTTAAAACCCCAT | 55230 |
rs745534584 | snp | G/T | 1.65806e-05 | 0.00287924 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233525545 | AAGAACCATGTCTCC[G/T]TCCCAAAATTCTAAC | 55230 |
rs745563205 | snp | C/T | 2.67627e-05 | 0.00365795 | stop-gained, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485899 | ACCCTGGGCCGCGTT[C/T]CACACCAGGTCCAGG | 55230 |
rs745600777 | in-del | -/T | 1.66916e-05 | 0.00288886 | frameshift-variant, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233524539 | CATCAGCAATTTCAG[-/T]TTCACACAGTGTCAG | 55230 |
rs745628897 | in-del | -/TAGTATATTATTTTTCC | 1.73972e-05 | 0.00294929 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233512650 | GAATATTATTTTTCT[-/TAGTATATTATTTTTCC]TAGAGAGCTAGGAAT | 55230 |
rs745635791 | snp | A/G | 9.70921e-05 | 0.00696682 | intron-variant | USP40 | GRCh38.p7 | 2:233561058 | AAGAGCATATTTGAT[A/G]ATTAATAAAATTATT | 55230 |
rs745668750 | snp | C/T | 3.46452e-05 | 0.0041619 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485599 | AATCTTGTTTTTTTT[C/T]CTTTTTCCTCTTGGT | 55230 |
rs745669996 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233480918 | CAGAGGGTGAGGCTG[C/T]GGGTGAGGAGGAAGG | 55230 |
rs745685040 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233560637 | GACTCCTAAGAAGTA[C/T]AAATTTGAGCCTGAA | 55230 |
rs745686227 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233513690 | CCTATATTTAAAATA[C/T]GTTGGGTGATTTTAT | 55230 |
rs745710955 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233498255 | AAATTCCTTCATGAG[C/T]TCAAATGTCATTTGT | 55230 |
rs745756926 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233540902 | GTAAGTTGATTCCAT[A/C]ATAATTATTTTATTA | 55230 |
rs745788739 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233511347 | TCTGTACCAGTGCCA[C/G]CTATAACTGCAGAAC | 55230 |
rs745812538 | snp | A/G | 1.86872e-05 | 0.00305667 | intron-variant | USP40 | GRCh38.p7 | 2:233556847 | CTAAAATACTCTGGC[A/G]TATTTACCTGCCTCT | 55230 |
rs745835102 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233479921 | GGCCGTGCTGCTTGC[A/G]GAGCTCACACAGTCC | 55230 |
rs745840049 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233481687 | CGTCAGTCTGTTCTC[A/G]CCTCTGTATTTCTAT | 55230 |
rs745840750 | snp | C/T | 1.65787e-05 | 0.00287907 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533596 | CTTTAGAATCATTTA[C/T]ATCAAACCAGTGGGG | 55230 |
rs745850338 | snp | A/G | 5.11731e-05 | 0.00505806 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233491192 | AGCTCCGCCAGCGTG[A/G]CATCTTCTGAGATCT | 55230 |
rs745864417 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233491350 | TTTTGATATTGTAAA[C/T]AGGTTATTAAAATTC | 55230 |
rs745939575 | snp | A/G | 0.000183766 | 0.0095838 | intron-variant | USP40 | GRCh38.p7 | 2:233488217 | GTGTGTGTCACTTCA[A/G]ATGCACAGGAGAATT | 55230 |
rs745942054 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233522799 | TTAGCCATAATGTTA[A/G]TACCTTCTTCAGGAA | 55230 |
rs745969011 | in-del | -/A | 1.86215e-05 | 0.00305129 | intron-variant | USP40 | GRCh38.p7 | 2:233549270 | TGATATAGTTTTCAT[-/A]AAATGCTGATAATAA | 55230 |
rs745969983 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233478945 | GATTTCTCAGTGAAC[C/T]TCTTTGGTGGCTTTT | 55230 |
rs746066110 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233552225 | AAAAAAAGTTGAATG[-/A]AAAAAAAAAAACAAA | 55230 |
rs746077953 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233521883 | AATTATGACAATGAC[C/T]GTAATATATTAACTA | 55230 |
rs746100909 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233549873 | ACATTTTCTATAATT[-/A]ATATGCTCCATAATC | 55230 |
rs746120850 | snp | A/T | 6.65048e-05 | 0.00576611 | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233561205 | CAAACCAAGCTCTTC[A/T]GGGCCAAGAGAAAAT | 55230 |
rs746124555 | snp | C/T | 8.3231e-05 | 0.00645047 | intron-variant | USP40 | GRCh38.p7 | 2:233523513 | ATACCAAGACAACCA[C/T]TAGTACAGCTGATAT | 55230 |
rs746141398 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233477525 | AGACACAGACACTGT[C/G]ATTGACTCATGGATG | 55230 |
rs746161012 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233496630 | TGATTGATAGCATTT[A/G]GGGAAAGTTCTCCCT | 55230 |
rs746184133 | snp | C/G | 1.65658e-05 | 0.00287795 | intron-variant | USP40 | GRCh38.p7 | 2:233559798 | CTCTTCCTTAAAGAG[C/G]TGATCCTCGTACCTC | 55230 |
rs746200004 | in-del | -/G | 5.09671e-05 | 0.00504787 | intron-variant | USP40 | GRCh38.p7 | 2:233481161 | AGAGAGAGTCAGAGA[-/G]GGCTCTGTCAGCTGC | 55230 |
rs746237105 | snp | A/C | 1.66765e-05 | 0.00288756 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233493440 | CTTGGCTGGAAGTGG[A/C]TCTCCAAACTCTGCC | 55230 |
rs746237317 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233565904 | ACAATAAGTAACAGC[C/T]GTTTTTAAAAAGGCA | 55230 |
rs746253089 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233484112 | GCAGTGAGCCAAGAT[C/T]GTACCACTGCACTCC | 55230 |
rs746264973 | in-del | -/C | 1.75296e-05 | 0.00296049 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477380 | GGGAGTAGAGCCGTG[-/C]CAGCGGCGCGGTTAT | 55230 |
rs746298271 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233500170 | TTCAAAGTTTCATCC[A/G]CCAACTCCCAGGTTT | 55230 |
rs746301709 | snp | A/G | 1.65666e-05 | 0.00287802 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556968 | CTAAAGAAGTTTCCA[A/G]AGCGCTGAAGAGGAT | 55230 |
rs746313230 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562932 | AGTGTATAGAGTAAG[G/T]TATAAATATTGCCAC | 55230 |
rs746324261 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233544051 | ACTCAGTCCCGTAAG[A/G]CTGTTCCCTACTTCA | 55230 |
rs746329858 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233544132 | GATTACAAATTCTAG[A/G]GTTCCCATCACCCCA | 55230 |
rs746340562 | snp | G/T | 3.38209e-05 | 0.00411209 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233521040 | TCTTCAGATTCTAAC[G/T]GGCATAAATTTTTAA | 55230 |
rs746350226 | in-del | -/TT | | | intron-variant | USP40 | GRCh38.p7 | 2:233514017 | TCTCACATAAATCTC[-/TT]GTCGACGGAAACAAT | 55230 |
rs746427554 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233544994 | AGAGACAAACACAAA[C/T]CTTTCTTGGAAGAAG | 55230 |
rs746430602 | snp | C/T | 2.71036e-05 | 0.00368118 | intron-variant | USP40 | GRCh38.p7 | 2:233527609 | AAAATACATAAATAC[C/T]GTGTTTTTATAACAG | 55230 |
rs746503565 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233516565 | TGGTGGCGGGCACCT[A/G]TAGTCCCAGCTACTC | 55230 |
rs746508800 | in-del | -/GGA | 5.23473e-05 | 0.00511575 | cds-indel, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477490 | AGCTGCTCTGCTCAT[-/GGA]GGGCTTCTTGGCTGC | 55230 |
rs746515937 | snp | A/C | 1.6574e-05 | 0.00287867 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233525514 | GAAGTCCTGCTGGTA[A/C]AAGCTTTGCAACACT | 55230 |
rs746517790 | snp | C/T | 4.82544e-05 | 0.00491171 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233510063 | CATCTCTCACAGATA[C/T]TGTTTCTTCTACTAC | 55230 |
rs746535958 | snp | A/C | | | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233566875 | TGTAACTCTTCTGCT[A/C]CAAGAGTTTGGGAAC | 55230 |
rs746588130 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233497278 | CCAGGAGGTCACACC[A/G]GACTGGAAGGGCAGG | 55230 |
rs746602320 | snp | A/G | 8.64715e-05 | 0.00657482 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233542276 | ACTATACCTCTAATA[A/G]GATTGCTTTTAGAAT | 55230 |
rs746609761 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233529277 | CAGAGTTAAAGTTAC[C/T]CTCACTATAAAAATT | 55230 |
rs746611217 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233500355 | TGTCTGAATTTCCCC[A/G]TTTTCCCTAAATATA | 55230 |
rs746629187 | in-del | -/AAAAAAAAAA | | | intron-variant | USP40 | GRCh38.p7 | 2:233509845 | GAGACTCTCTAAAAA[-/AAAAAAAAAA]AAAAAAAAAATCCAG | 55230 |
rs746660682 | snp | G/T | 1.65734e-05 | 0.00287862 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233540751 | CCAGCTGATCAACAG[G/T]AATTAGATTATTCTC | 55230 |
rs746711122 | snp | A/G | 3.8981e-05 | 0.00441463 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233493534 | CTGGTACCACCAGAT[A/G]GGCACCTTCAGGAAA | 55230 |
rs746716991 | snp | A/G | | | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233565461 | ATTCTCTAGGAGCAG[A/G]TGGCTCCAAAGCTTT | 55230 |
rs746723190 | snp | A/T | 1.82314e-05 | 0.00301916 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485798 | AGCCACTCGAACTTT[A/T]CGGGAAAGTATTTGG | 55230 |
rs746793496 | snp | A/G | 6.86955e-05 | 0.00586029 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233481283 | GAAATCATCATCGTC[A/G]TCAATCAGGAGATTC | 55230 |
rs746794360 | in-del | -/AA | 7.55772e-05 | 0.00614678 | intron-variant | USP40 | GRCh38.p7 | 2:233549069 | TAGAAAAGAAATTGC[-/AA]AGATATTTCTAAACG | 55230 |
rs746794965 | snp | C/T | 1.65784e-05 | 0.00287905 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533589 | GGCTGGACTTTAGAA[C/T]CATTTATATCAAACC | 55230 |
rs746796389 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233524627 | CTGAGCTAAAGAAAG[A/G]GCTGAGACAAATATT | 55230 |
rs746809729 | in-del | -/AG | 1.66768e-05 | 0.00288758 | intron-variant | USP40 | GRCh38.p7 | 2:233525586 | TATTAATGAAGGAAA[-/AG]AGAATGTTGAAAAGT | 55230 |
rs746835324 | snp | C/T | 0.000143767 | 0.00847719 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233491182 | CTGAGACTTCAGCTC[C/T]GCCAGCGTGGCATCT | 55230 |
rs746845213 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233557816 | AGAGGAACAAATGGA[C/G]AGTTCAGAAGCAGAG | 55230 |
rs746882858 | snp | C/T | 1.69772e-05 | 0.00291347 | intron-variant | USP40 | GRCh38.p7 | 2:233533471 | TAGGAACATTTTTCT[C/T]TCCATACCTTCAGGG | 55230 |
rs746883228 | snp | C/T | 6.25215e-05 | 0.00559078 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233489450 | GGGCTGGGGACGGGA[C/T]ACCGAACTCCAGGAA | 55230 |
rs746894831 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233551171 | GAGTGAGGCTGCTAC[C/T]GTCATCCAGTAGGTA | 55230 |
rs746980293 | snp | A/G | 1.73495e-05 | 0.00294524 | intron-variant | USP40 | GRCh38.p7 | 2:233554347 | CTAACTACAAAGTGG[A/G]GACCCTGGGAAAAAG | 55230 |
rs747028487 | snp | C/T | 3.08513e-05 | 0.00392743 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233549134 | CAAATGATCAACATC[C/T]TTAATATATACATGG | 55230 |
rs747030105 | in-del | -/GT | | | intron-variant | USP40 | GRCh38.p7 | 2:233517784 | TAAAGAAACTGTGGT[-/GT]GTGTGTGTGTGTGTG | 55230 |
rs747036288 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233538905 | GTGGCCAGGTGTGCC[C/T]GTGGTCGCAACTACT | 55230 |
rs747053337 | snp | A/T | 0.00012809 | 0.00800179 | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233561182 | TCGGGTTTATCCTTA[A/T]CTTCAAACAAACCAA | 55230 |
rs747065068 | snp | A/G | 5.06163e-05 | 0.00503046 | stop-gained, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233498595 | ACCAATCCATTTTTC[A/G]TAAATGCCAGGCATC | 55230 |
rs747089179 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233534768 | TTCTTTTCATTTTTT[C/G]TTCTTTGGGTTTTTA | 55230 |
rs747100552 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477386 | TAGAGCCGTGCAGCG[G/T]CGCGGTTATCTGAAG | 55230 |
rs747167911 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233547575 | GCTTTAAGCATTTTA[C/T]ATCCTAACATTACGG | 55230 |
rs747244610 | snp | C/T | | | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233567690 | TATATAAGATTATAG[C/T]TATATAACCTTATAT | 55230 |
rs747259576 | snp | C/T | 5.34669e-05 | 0.00517016 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533714 | CTGGAGAGAACTATT[C/T]TTCAAGAGACGAACT | 55230 |
rs747270218 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233509839 | GAGTTGAGACTCTCT[-/A]AAAAAAAAAAAAAAA | 55230 |
rs747295847 | snp | C/T | 3.3123e-05 | 0.00406945 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523309 | CACTGTTGATGAAGA[C/T]GACACCTGCTGGGAT | 55230 |
rs747298655 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233548433 | ATCAATGCTCATTTT[A/G]TTTTTCAGAAAAAAT | 55230 |
rs747302350 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543876 | CCCATACAGGGCAGA[C/G]TTGGGGAGAGAAAGC | 55230 |
rs747311438 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233492916 | GCGGCTGAGTGCTGA[C/G]TAAGACAACATGCTT | 55230 |
rs747313933 | snp | C/T | 5.34478e-05 | 0.00516924 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485513 | TCAAAGTGGTAAATT[C/T]GCTGTTAAACAACTT | 55230 |
rs747370691 | snp | A/G | 2.32826e-05 | 0.00341186 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233519629 | CTAGTTCCTTCATTA[A/G]TTTTAATTCCTTTAT | 55230 |
rs747399199 | in-del | -/T | 7.29102e-05 | 0.00603737 | intron-variant | USP40 | GRCh38.p7 | 2:233488351 | TGACATAACATTTAA[-/T]TTTCTTGAATTTTTT | 55230 |
rs747401248 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233494112 | CACTTAATTTCCAAC[A/T]ATAGAAGATGAGAAT | 55230 |
rs747442295 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477318 | GCCAGGCAGCCAGTC[C/T]CCATGCCCAGGAAAC | 55230 |
rs747450600 | in-del | -/TCG | 3.32e-05 | 0.00407417 | cds-indel, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233481278 | GTACTGAAATCATCA[-/TCG]TCGTCAATCAGGAGA | 55230 |
rs747458998 | snp | C/T | 1.68278e-05 | 0.00290062 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527508 | GGTGCAGAGCCCCAT[C/T]GAAGAAATGATACTG | 55230 |
rs747480660 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233519394 | TATCTGGGGAAGGAG[A/T]GAAAGAATAGGTCTG | 55230 |
rs747486620 | snp | C/T | 1.70301e-05 | 0.00291801 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477395 | GCAGCGGCGCGGTTA[C/T]CTGAAGCTCCCCACG | 55230 |
rs747558188 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233478174 | GTAATTTTGGGGATA[C/T]CCTGGTAGGCACGCG | 55230 |
rs747571307 | snp | A/T | 8.13901e-05 | 0.00637875 | intron-variant | USP40 | GRCh38.p7 | 2:233549263 | AAAATATTGATATAG[A/T]TTTCATAAAATGCTG | 55230 |
rs747575462 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233507078 | CACAAAAAATGCTCA[A/G]CATCACAAATCATAA | 55230 |
rs747580555 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233542872 | CTAGCACAATACACA[C/T]AGTGGGTTCCAATAT | 55230 |
rs747590243 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233529102 | CATGGCAGGCTCTCT[C/T]TGGACCCAAGGAAAT | 55230 |
rs747592624 | in-del | -/TCTT | 3.45922e-05 | 0.00415871 | intron-variant | USP40 | GRCh38.p7 | 2:233493382 | CAGTCAATTTACTTC[-/TCTT]TATGATGCACTGGCT | 55230 |
rs747656330 | snp | A/G | 1.65712e-05 | 0.00287843 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233540739 | AAAGTTTCTGGCCCA[A/G]CTGATCAACAGGAAT | 55230 |
rs747660443 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233482067 | CTTCAATGACTGAGA[G/T]ATTAACCAGGCTCTG | 55230 |
rs747679532 | snp | C/G/T | 5.30615e-05 | 0.00515057 | intron-variant | USP40 | GRCh38.p7 | 2:233524464 | CATCCAAAATTATCA[C/G/T]GAATATTTCTTCAGT | 55230 |
rs747680077 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233563906 | CGCTCCATGACCCGC[A/C]CTACACTTCACCATC | 55230 |
rs747718743 | snp | C/G | 1.98261e-05 | 0.00314844 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485667 | TAAGCAAAACTCAAC[C/G]TCAAGTTCTCACTAA | 55230 |
rs747727874 | in-del | -/C | 1.69427e-05 | 0.00291051 | frameshift-variant, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485538 | CAACTTACCTTAACA[-/C]CAATAGTATCTCCGT | 55230 |
rs747745744 | snp | C/T | 1.66081e-05 | 0.00288163 | intron-variant | USP40 | GRCh38.p7 | 2:233540658 | AAACGATGCCATGTA[C/T]TACCTTCCGCAGTGG | 55230 |
rs747781989 | snp | C/T | 1.88269e-05 | 0.00306808 | intron-variant | USP40 | GRCh38.p7 | 2:233477527 | ACACAGACACTGTCA[C/T]TGACTCATGGATGCA | 55230 |
rs747808751 | snp | A/G | 9.61862e-05 | 0.00693425 | intron-variant | USP40 | GRCh38.p7 | 2:233493326 | TTTTCAAGATCTTAC[A/G]TTTTAAAAATAAATA | 55230 |
rs747835734 | snp | C/G | 3.31296e-05 | 0.00406985 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556950 | CATGACCGGAGGTCC[C/G]AACTAAAGAAGTTTC | 55230 |
rs747849960 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233481375 | AGGCATGTCTAAAAA[A/T]CTACCTATATTGACA | 55230 |
rs747862076 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233479119 | ACCATGAATTTTTAA[A/T]ATGTGCTATCTCAAA | 55230 |
rs747869663 | snp | C/T | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233487430 | GGTTTAAAATGTCCA[C/T]ACCATTTGATCCTGG | 55230 |
rs747943635 | snp | A/C | 3.38765e-05 | 0.00411547 | intron-variant | USP40 | GRCh38.p7 | 2:233489328 | CCAGTGCGTCAGCAG[A/C]AGAGAGGGACAGTGT | 55230 |
rs747944872 | snp | A/C | 3.24249e-05 | 0.00402634 | splice-acceptor-variant, intron-variant | USP40 | GRCh38.p7 | 2:233551520 | ACGTAATTTGGCCGA[A/C]TGTTAAAAGAAAAAT | 55230 |
rs747947403 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233537123 | TCCTGGGCTCAAGCA[A/G]TCCTCTTGCCTAGAC | 55230 |
rs747952403 | snp | C/G | 1.84561e-05 | 0.00303772 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551439 | GCTAGTTTCCTTGTA[C/G]CGTTCGCATTTCACA | 55230 |
rs747979914 | snp | C/T | 4.4826e-05 | 0.00473402 | intron-variant | USP40 | GRCh38.p7 | 2:233510160 | AGACAGATGTGTAAA[C/T]GCAATTTAATCTGAA | 55230 |
rs747988834 | snp | C/T | 7.3295e-05 | 0.00605327 | intron-variant | USP40 | GRCh38.p7 | 2:233510012 | GCAAACATACAAACA[C/T]ACACAGCCTCTGAAA | 55230 |
rs747994326 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233478346 | TCAACACACGAGTCT[C/T]TCCCACTTTAGTGTT | 55230 |
rs747996622 | snp | A/G | 0.000114371 | 0.00756123 | missense, upstream-variant-2KB, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233565503 | TCTTCCCTTTTCCAT[A/G]CTGATTATTAGACAC | 55230 |
rs748008749 | in-del | -/A | 0.000106843 | 0.00730823 | intron-variant | USP40 | GRCh38.p7 | 2:233549236 | AATTCACTCTAAAAG[-/A]AAAAAAGAACAAAAA | 55230 |
rs748013231 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233565039 | AAATCTTAAAACTCA[A/G]ACAGTGTAACAATAA | 55230 |
rs748054826 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233531913 | AGGCAGGAGAATAGG[A/G]TCTGGAGACAGGGAA | 55230 |
rs748106209 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233500608 | TAAAAGAAAAATGGC[-/A]AAAAAAAACCCCACC | 55230 |
rs748108338 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233533142 | TTCAAAGGCAACATA[C/T]GGCTGAATGACAGAG | 55230 |
rs748126686 | in-del | -/AG | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233475601 | CCAAATTAAAAAAAC[-/AG]AAAACAGGAAGAAAG | 55230 |
rs748158624 | snp | C/T | 1.658e-05 | 0.00287919 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233559924 | AAGGGATGATTCGAA[C/T]CTGAATGAGAAACAA | 55230 |
rs748159675 | snp | A/C/G | 0.00012616 | 0.00794138 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233499915 | GCATTAACTTTAAAC[A/C/G]CTGTAAAGAAAAACA | 55230 |
rs748231128 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233547283 | GAAAACACAAAATTT[A/C]GGCATAGATCATCTC | 55230 |
rs748232601 | snp | A/G | 3.39132e-05 | 0.0041177 | intron-variant | USP40 | GRCh38.p7 | 2:233496710 | TCATCTCTGTAATCA[A/G]ATAACAATTATTACT | 55230 |
rs748235013 | snp | A/G | 1.65619e-05 | 0.00287762 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523298 | TGGACATCCAGCACT[A/G]TTGATGAAGATGACA | 55230 |
rs748240499 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233558001 | GTGAGACCTCATCTC[-/A]AAAAAAAAAAAAAAA | 55230 |
rs748260896 | snp | A/C/T | 3.31539e-05 | 0.00407137 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533572 | TATCCTTTTCCCTGA[A/C/T]TGGCTGGACTTTAGA | 55230 |
rs748274566 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233537622 | AATGACAGTTGGCTT[C/G]TCATCCAACATACTG | 55230 |
rs748284652 | snp | C/T | 1.8758e-05 | 0.00306246 | intron-variant | USP40 | GRCh38.p7 | 2:233485489 | AAATCATGTGACCCT[C/T]GTGTCTTCTCAAAGT | 55230 |
rs748341601 | in-del | -/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233519529 | GTTCTCCCTAAACTG[-/T]TTTTTTGTATTCTCC | 55230 |
rs748341999 | snp | A/G | | | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233481277 | TGTACTGAAATCATC[A/G]TCGTCGTCAATCAGG | 55230 |
rs748381445 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233546423 | ATGCATCAAAAAACT[A/G]AGGATAAATATTGCC | 55230 |
rs748383006 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233512028 | TGCTAAATGGAAGCT[A/G]TGAAAGTCTAGTTTC | 55230 |
rs748403837 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233505228 | CAGCAATAGATGCCT[A/T]GATCAAAAATGAAGA | 55230 |
rs748430224 | snp | A/G | 4.77316e-05 | 0.00488503 | intron-variant | USP40 | GRCh38.p7 | 2:233481175 | AGGGCTCTGTCAGCT[A/G]CACATCTGTGCAGAC | 55230 |
rs748433427 | snp | A/C/T | 0.000157525 | 0.00887361 | intron-variant | USP40 | GRCh38.p7 | 2:233533439 | GTTTATCTTCTAAAG[A/C/T]CATTAACTGAAACAA | 55230 |
rs748441123 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233497110 | AGATGAAATTTTAAT[C/T]AATCCTAAAAAGATG | 55230 |
rs748497421 | snp | A/T | 1.71085e-05 | 0.00292471 | intron-variant | USP40 | GRCh38.p7 | 2:233527394 | GAATTAAGAGGAAGT[A/T]AGGCGATATTACCTG | 55230 |
rs748554469 | snp | A/G/T | 9.65939e-05 | 0.00694901 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477366 | GCCGGAGAGTTCATC[A/G/T]GGAGTAGAGCCGTGC | 55230 |
rs748567637 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233526449 | TTCAGAAATATTAGA[C/T]AACTTTAGAAATCCT | 55230 |
rs748585654 | snp | C/T | 3.3206e-05 | 0.00407455 | splice-acceptor-variant | USP40 | GRCh38.p7 | 2:233525563 | CCAAAATTCTAACAG[C/T]TGAAGAATATTAATG | 55230 |
rs748597775 | snp | G/T | 0.000246853 | 0.011107 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233549108 | ATACGTACTTGAAAC[G/T]GCCAGTTTCCCAAAT | 55230 |
rs748659200 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233520054 | CTATGTCAGGAATGA[C/T]GAATGTGGGGCCAGT | 55230 |
rs748687678 | snp | C/T | 3.60412e-05 | 0.00424492 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233542361 | TGGTTTACTTTTTTC[C/T]TCCTAGGAAGGAAAA | 55230 |
rs748717168 | snp | C/T | 1.66114e-05 | 0.00288192 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233496804 | AAAGTATCTCCAGAA[C/T]ATATCAGAAGTTCTT | 55230 |
rs748721671 | snp | C/T | 0.000104849 | 0.00723973 | intron-variant | USP40 | GRCh38.p7 | 2:233561016 | CCATTACCCATAGGG[C/T]ATAGGCCAAGTCACT | 55230 |
rs748739785 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233491557 | GCTGCATTCTGTATG[G/T]TAGCTTCCTGTTTCC | 55230 |
rs748776669 | snp | C/T | 1.65674e-05 | 0.00287809 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556937 | CGATAGATGAGGTCA[C/T]GACCGGAGGTCCCAA | 55230 |
rs748807382 | snp | G/T | 1.70432e-05 | 0.00291913 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485532 | GTTAAACAACTTACC[G/T]TAACACCAATAGTAT | 55230 |
rs748825580 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233481099 | GCTTTGTGTGCACTC[C/T]GAATCAACAAGAGTT | 55230 |
rs748831872 | in-del | -/TTTTCTTAGTATATTAA | 3.44869e-05 | 0.00415238 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233512644 | TAAAAGGAATATTAT[-/TTTTCTTAGTATATTAA]TTTTCTTAGAGAGCT | 55230 |
rs748832303 | snp | A/T | 2.61366e-05 | 0.00361492 | intron-variant | USP40 | GRCh38.p7 | 2:233491286 | GACAGAGCGGGATGT[A/T]TACAAGGAACTTGAA | 55230 |
rs748859605 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233503681 | AGCAAAGCTATCCTT[C/G]AGAAATAAAGGCGAG | 55230 |
rs748886817 | in-del | -/A | 1.72791e-05 | 0.00293926 | intron-variant | USP40 | GRCh38.p7 | 2:233498536 | AAGTACAATGTATAG[-/A]AATCATCTTACTTCT | 55230 |
rs748920091 | snp | A/C | 8.81562e-05 | 0.00663855 | intron-variant | USP40 | GRCh38.p7 | 2:233519592 | CTAAACTAAGAACCG[A/C]AAAGAAAATGTAAAT | 55230 |
rs748978080 | snp | C/G | 1.67722e-05 | 0.00289583 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527494 | TTGAGAGACTACTGG[C/G]TGCAGAGCCCCATTG | 55230 |
rs749020795 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233499637 | CCAACACTGTAAAAC[A/T]TTCCTACTTTGTACC | 55230 |
rs749020972 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233526610 | TAACTAATTTCTGGG[-/A]AAAAAACACAAAAAA | 55230 |
rs749034570 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233541126 | CGTAAGTACAAAAAC[A/G]AAGATGATTAATGTC | 55230 |
rs749058672 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233548650 | AACATAACTATTAGA[C/T]AACAGTATTATATCA | 55230 |
rs749071927 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233515049 | CTTGGCATAATGACT[C/T]TGAGATGCATTCATG | 55230 |
rs749077467 | snp | A/C | 1.77941e-05 | 0.00298274 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233499888 | ACTTACCTTGTAGGC[A/C]AGATTTCTTCAGCAT | 55230 |
rs749106363 | snp | A/T | 6.89869e-05 | 0.00587271 | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233561218 | TCTGGGCCAAGAGAA[A/T]ATAAAGTTCATATGG | 55230 |
rs749120514 | snp | C/T | 2.53862e-05 | 0.00356265 | intron-variant | USP40 | GRCh38.p7 | 2:233523539 | GATATTTGCCAACAC[C/T]GTCAACATAACATGG | 55230 |
rs749134598 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233527745 | TTTTCAGTCAATAGC[A/T]AAAATTCAGTTCTGT | 55230 |
rs749135851 | snp | C/G | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486304 | AGGGACAGGGTGAGA[C/G]AGGCCTGGCTTGATA | 55230 |
rs749179280 | snp | C/T | | | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233512333 | TAACTAGATCAAACC[C/T]GTGAGTAAAATGAGA | 55230 |
rs749266361 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233495579 | TATCTCTTAATAAAC[A/C]TATTAAAATTCTTCA | 55230 |
rs749276098 | snp | A/G | 1.68966e-05 | 0.00290655 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523454 | TAAAAGTAGAGGTTC[A/G]CAGTCAATACCAGTT | 55230 |
rs749295979 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233547676 | CTAGACACCGGTTAG[C/T]ACTTTCCCTCAGAAC | 55230 |
rs749304889 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233563783 | GCTAAGCTATACAAG[C/T]AGTGCACATTGTGCA | 55230 |
rs749354263 | in-del | -/TC | 1.67349e-05 | 0.0028926 | frameshift-variant, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527474 | AAATCCCACACGCTT[-/TC]TGTTTGAGAGACTAC | 55230 |
rs749362345 | snp | A/C | 0.000157356 | 0.00886868 | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233529557 | TTGGCTAAATGAAAT[A/C]TGGTTGCTGGAAGAG | 55230 |
rs749381974 | in-del | -/TG | | | intron-variant | USP40 | GRCh38.p7 | 2:233512891 | AGTACCTGGTCAAAC[-/TG]TGCAAAACAATATTA | 55230 |
rs749416361 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233497035 | ATAAGCTGTAAGTCT[C/G]ACAGAAGAACTGAGG | 55230 |
rs749416722 | snp | C/T | 8.06354e-05 | 0.00634911 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551506 | AAAGGAGGCAGCTTA[C/T]GTAATTTGGCCGACT | 55230 |
rs749436409 | in-del | -/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233482363 | AGTGAGACTCTGTCT[-/C]AAAAAAAAAAAAAAA | 55230 |
rs749452008 | snp | A/G | 1.66142e-05 | 0.00288216 | intron-variant | USP40 | GRCh38.p7 | 2:233527618 | AAATACTGTGTTTTT[A/G]TAACAGACACTGTGT | 55230 |
rs749493741 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233515813 | TCCCAGAAATTTTGT[A/T]GTTTTAGGTTTTAAC | 55230 |
rs749556913 | snp | A/T | 3.51624e-05 | 0.00419284 | intron-variant | USP40 | GRCh38.p7 | 2:233488229 | TCAGATGCACAGGAG[A/T]ATTTCTTACCCCAAG | 55230 |
rs749559540 | snp | A/C | 0.000106872 | 0.00730921 | stop-gained, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551432 | TATAACAGCTAGTTT[A/C]CTTGTAGCGTTCGCA | 55230 |
rs749560692 | snp | C/T | 3.78939e-05 | 0.00435264 | intron-variant | USP40 | GRCh38.p7 | 2:233499961 | TTTCTGTTTCTGAGT[C/T]ACAGTTCTAGGACAA | 55230 |
rs749588680 | snp | A/G | 7.70386e-05 | 0.00620592 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233542296 | GCTTTTAGAATCATC[A/G]GTGGATGATCAATCT | 55230 |
rs749596753 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233518925 | GGAATACTAGACTAG[C/T]CAGCAATGCAAAGGA | 55230 |
rs749646234 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233551614 | AAACAACCTATGACA[C/G]AGTTCTAAGAGAAAT | 55230 |
rs749646671 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476294 | AGGTGACAAGCAGGC[C/T]CAGGACATGCGACAC | 55230 |
rs749662961 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476788 | TGTGTGGCTCCTCCT[C/T]GTGGAAAGAGCTCGC | 55230 |
rs749664787 | snp | A/G | 0.000148282 | 0.00860923 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485851 | AAGACGATAGAAATC[A/G]GCAACTCTCTGCCTC | 55230 |
rs749670171 | in-del | -/TTAAAC | | | intron-variant | USP40 | GRCh38.p7 | 2:233504826 | ATCAACAAAGAAACA[-/TTAAAC]TTAAACTTCACCATA | 55230 |
rs749671635 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233500038 | TGATTCTTGAATAGG[A/C]AAGGATAGACATAGT | 55230 |
rs749725729 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233491859 | TCATCAAAAACAATA[C/T]AAAAGCTGGCAACTA | 55230 |
rs749738614 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233546311 | AGGAAGAGAGAAATC[A/C]CTACTCTCAAAACAT | 55230 |
rs749740759 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233531296 | TTTTTACTGATACAG[A/C]AAATTCTCCCTCAGT | 55230 |
rs749742152 | snp | A/G | 4.97244e-05 | 0.00498596 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233540758 | ATCAACAGGAATTAG[A/G]TTATTCTCCTCCTTA | 55230 |
rs749754400 | snp | A/G | 2.29087e-05 | 0.00338435 | intron-variant | USP40 | GRCh38.p7 | 2:233493568 | TGAAGAATGGAGCAT[A/G]TTTAACTGCTGTGAT | 55230 |
rs749836706 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233483347 | ATACAAAAAATTAGC[C/T]GGGCATAATGGCACG | 55230 |
rs749849479 | snp | C/T | 1.79322e-05 | 0.00299429 | intron-variant | USP40 | GRCh38.p7 | 2:233523146 | TGACTTTTAGAAATC[C/T]TTTTTCTCTTGTTAG | 55230 |
rs749880978 | in-del | -/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233517667 | GCTGGGATTACAGGC[-/G]TGAGCCACTGTGCCC | 55230 |
rs749915745 | in-del | -/A | 1.67402e-05 | 0.00289306 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556875 | CTCGCTAACGTTCTT[-/A]ACATTCTTTACAAAC | 55230 |
rs749918187 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476664 | AGTCCTCGGGATCCA[A/C]GGACCTTCTGATCAC | 55230 |
rs749922721 | in-del | -/C | 3.33084e-05 | 0.00408082 | intron-variant | USP40 | GRCh38.p7 | 2:233540815 | TCTGATGAGAAATAA[-/C]TTGCATACTTAACAA | 55230 |
rs749926974 | snp | A/C | 0.000467563 | 0.0152828 | intron-variant | USP40 | GRCh38.p7 | 2:233488021 | CCTGGTGATTACTGA[A/C]AAATTAATTCTCCCT | 55230 |
rs749939937 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233534400 | ATCCACTACGCCCCT[A/G]TCCTCTCACTCTTTA | 55230 |
rs749943547 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233519510 | TTTGGGTGGTAGGTA[C/T]GTGAGTTCTCCCTAA | 55230 |
rs749993077 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233520897 | AGCTGAAGTCTATTG[A/C]GACAACTGTTCTGAA | 55230 |
rs749996244 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233546938 | CACAGTAGATGAGGA[C/T]AACAAGTGTTTAACT | 55230 |
rs750014094 | snp | A/G | 1.67066e-05 | 0.00289016 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233549213 | TCATATATATATTCT[A/G]AGTCATCCAATTCAC | 55230 |
rs750014824 | snp | A/C | 3.52491e-05 | 0.00419801 | intron-variant | USP40 | GRCh38.p7 | 2:233498641 | AAAATTGGGATAAAA[A/C]AAATTCAAAGTTAGG | 55230 |
rs750017762 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233477828 | AAGAATAACATCCGG[-/A]GTGCACACACACCGC | 55230 |
rs750051353 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233532907 | GCACTCCAGCCTGGA[C/T]GAGAGAGTGAGGCTG | 55230 |
rs750075053 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233484667 | TTGTATTTTTTTGTA[A/G]AGACCAGGTTTCACT | 55230 |
rs750081555 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233498832 | ATCTCACCTGGAAAG[C/T]TGCTTCAGTTATCTT | 55230 |
rs750100743 | snp | A/G | 0.000156384 | 0.00884125 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233549104 | TTCTATACGTACTTG[A/G]AACTGCCAGTTTCCC | 55230 |
rs750102545 | snp | C/T | 7.07889e-05 | 0.0059489 | intron-variant | USP40 | GRCh38.p7 | 2:233561152 | CCAGTAAATCATAGA[C/T]GTAATACCTTTGCAT | 55230 |
rs750105535 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233531576 | GTGAATTCTGATACA[A/C]AATATTTTTACCAGA | 55230 |
rs750144689 | snp | C/T | 3.48481e-05 | 0.00417406 | intron-variant | USP40 | GRCh38.p7 | 2:233498529 | CATACGAAAGTACAA[C/T]GTATAGAAATCATCT | 55230 |
rs750184063 | snp | C/T | 1.66098e-05 | 0.00288177 | intron-variant | USP40 | GRCh38.p7 | 2:233557023 | TTGCCTCATTTCCTA[C/T]AAAACAGGTAACTTT | 55230 |
rs750202931 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233527651 | TATCTCAAACCAAAG[A/G]TATCTGGCTTACAAT | 55230 |
rs750202936 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543361 | ATCTTAAACACACCA[C/T]GAGCTTGCAAGAACA | 55230 |
rs750218908 | snp | G/T | 1.67186e-05 | 0.0028912 | intron-variant | USP40 | GRCh38.p7 | 2:233540631 | GAAATTTCTTGGGAC[G/T]AGGACTTCCCAAAAC | 55230 |
rs750254251 | snp | C/G | 0.000185255 | 0.00962254 | intron-variant | USP40 | GRCh38.p7 | 2:233493402 | ATGATGCACTGGCTG[C/G]TGAAATCCCATTCTG | 55230 |
rs750320082 | snp | A/C | 3.31367e-05 | 0.00407029 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556931 | TACAGACGATAGATG[A/C]GGTCATGACCGGAGG | 55230 |
rs750324288 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233554201 | GTTGGGTGAACTGTT[C/G]GGTTGAAAGCCTTAA | 55230 |
rs750327312 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233542583 | GCCAGGAGGTTGAGG[C/G]GGGAGGACTGCTTGA | 55230 |
rs750331185 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233555433 | TTGTTAACTCATGGT[A/G]AAGATTTCAAGTACC | 55230 |
rs750342299 | snp | C/T | 2.4271e-05 | 0.00348352 | intron-variant | USP40 | GRCh38.p7 | 2:233491273 | GCACCTTCCAAAGGA[C/T]AGAGCGGGATGTTTA | 55230 |
rs750364079 | snp | A/T | | | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233542293 | ATTGCTTTTAGAATC[A/T]TCAGTGGATGATCAA | 55230 |
rs750376024 | snp | A/G | 1.78844e-05 | 0.0029903 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233512654 | TATTATTTTTCTTAG[A/G]GAGCTAGGAATTAAT | 55230 |
rs750393291 | snp | C/T | | | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475458 | CGTGAGCCACCGCGC[C/T]CGGCCAAAAGTTCCT | 55230 |
rs750415864 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233534283 | GGCAGACAAGCTCAG[-/A]AAAATCAAAGCATAG | 55230 |
rs750422457 | snp | A/G | 3.5241e-05 | 0.00419753 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527549 | TGAAGATGCAATTCA[A/G]AAGTATTGTTTGCAG | 55230 |
rs750432116 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233506399 | AACAATGAAACTACT[A/G]AAGGAAAACATAGGG | 55230 |
rs750501824 | snp | C/T | 0.00011424 | 0.00755691 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233565397 | GTCTGAAGAAGGGAA[C/T]TGAGGTAACAGGTTC | 55230 |
rs750504779 | snp | G/T | 0.000100194 | 0.0070772 | intron-variant | USP40 | GRCh38.p7 | 2:233525437 | CCGGACAAAAATGTA[G/T]ATATATAGAGTGAGT | 55230 |
rs750511479 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233488476 | ATCCTTGCTGCGGTG[A/C]TTATTTAGATACTTG | 55230 |
rs750511875 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233538134 | GTAATCGCTAGATGA[A/C]ATTAAATAGATTAAA | 55230 |
rs750514841 | in-del | -/G | 0.00127925 | 0.0252584 | intron-variant | USP40 | GRCh38.p7 | 2:233510034 | CCTCTGAAAACAAAA[-/G]GTAAAATTACTTACA | 55230 |
rs750517366 | snp | C/T | 1.86086e-05 | 0.00305024 | intron-variant | USP40 | GRCh38.p7 | 2:233499952 | AATGTTAGTTTTCTG[C/T]TTCTGAGTTACAGTT | 55230 |
rs750592498 | snp | A/C | 1.66715e-05 | 0.00288712 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233524522 | CACAAAGATGTCTTC[A/C]CCATCAGCAATTTCA | 55230 |
rs750612105 | snp | A/C | 5.61256e-05 | 0.00529714 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233561270 | GCCAAGTCAATCCTA[A/C]GCCAAAAGAACAAAG | 55230 |
rs750642698 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233522576 | ATATTGCAGTTACAG[C/T]GTATGACACATTGAC | 55230 |
rs750648607 | snp | A/G | 1.8412e-05 | 0.00303408 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485816 | GGAAAGTATTTGGCA[A/G]TTTCAATCTTCTCCA | 55230 |
rs750667498 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233518096 | ACTGCTCGTGTGATA[A/G]GTGCACCAAAATCTC | 55230 |
rs750692180 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233501474 | TCACTCAACTTTTTA[C/T]AAGAACAGACCCTGG | 55230 |
rs750696300 | snp | C/G | 1.65696e-05 | 0.00287828 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233540701 | TCTGTACTTCTTGTT[C/G]CAAGATATTCCTATC | 55230 |
rs750697930 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233525745 | AAATTAGTCAAAGCC[A/G]AAGACGGCTAATCTC | 55230 |
rs750710786 | in-del | -/CAAA | 3.5223e-05 | 0.00419646 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486008 | GTCAAGCGCCAGATC[-/CAAA]CAAACAAACAAAACC | 55230 |
rs750725675 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233550862 | GACTTTCTAGATGCA[C/T]AAATTCATCATTACA | 55230 |
rs750755612 | snp | C/T | 0.000201674 | 0.0100397 | intron-variant | USP40 | GRCh38.p7 | 2:233559947 | AGAAACAAACACATT[C/T]CTAAATGAATTCTTT | 55230 |
rs750780699 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233480374 | GTCGGGGAGTGGGGG[A/T]GGATGAGGACGCCTG | 55230 |
rs750792832 | snp | C/G/T | 3.31566e-05 | 0.00407154 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533526 | TAAAACAACATGTAG[C/G/T]CACTTTCTTTACCCT | 55230 |
rs750834185 | snp | C/T | 5.86355e-05 | 0.00541427 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233529509 | TATCTTGGATTAGCT[C/T]GAGCTGTGAACAAAA | 55230 |
rs750836992 | snp | C/T | 2.90069e-05 | 0.00380823 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233481235 | GGCCCGTTGTTTCTG[C/T]TTTTCTTTTCCAGTG | 55230 |
rs750852801 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233479438 | CATAGTGGTGCACGC[C/T]TGTAGTACCAGCTAC | 55230 |
rs750860688 | snp | C/T | 8.05056e-05 | 0.006344 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233489404 | AAAAGCCTGCCTGGG[C/T]GCTTCCTCTCCACCG | 55230 |
rs750898092 | snp | A/G | 1.6601e-05 | 0.00288101 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233554421 | AAGTTCCACAGTGGT[A/G]CAAGTTGTCACAATC | 55230 |
rs750898632 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477191 | ACATCCAGAGCTGCA[C/T]CAGCCCCCGTGGCTG | 55230 |
rs750908833 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233503052 | GTATATTTATGAAAT[A/G]CCTGAAGAGAAATTC | 55230 |
rs750983172 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233525648 | GTGCCAACTCACATA[C/T]GAAGATGACACAGAG | 55230 |
rs750986140 | snp | C/T | 3.39046e-05 | 0.00411718 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233510112 | AGGTTGAACGTCACT[C/T]CCCATTGCAAAAAAC | 55230 |
rs750993295 | snp | A/T | 2.42251e-05 | 0.00348022 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551493 | TGAAACAGTAAGAAA[A/T]GGAGGCAGCTTACGT | 55230 |
rs750996065 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233558767 | TTCTGTGGCATGTAA[A/G]TTACATCTCAATACA | 55230 |
rs751016165 | snp | A/G | 3.34007e-05 | 0.00408647 | intron-variant | USP40 | GRCh38.p7 | 2:233549093 | TCTAAACGAATTTCT[A/G]TACGTACTTGAAACT | 55230 |
rs751022191 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233484034 | TGCCTCCATGCTGCA[C/G]TGTCGCCACAGCTGT | 55230 |
rs751081140 | snp | A/G | 5.27802e-05 | 0.00513686 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485894 | GTCCCACCCTGGGCC[A/G]CGTTCCACACCAGGT | 55230 |
rs751092028 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233485125 | TATTTTATGCTTTTT[C/G]TGCATCTCTTGAGTC | 55230 |
rs751097070 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233531781 | ACAATATTCTCATCT[A/C]TAATAATAGATATGT | 55230 |
rs751102661 | snp | C/T | 0.000111601 | 0.00746914 | intron-variant | USP40 | GRCh38.p7 | 2:233560957 | TTTATAAAGCAGTAG[C/T]AGTATTGTACTTGGA | 55230 |
rs751120975 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233558613 | GGCTGAGTTGAGGGG[G/T]ATGGAAAGTTACTGC | 55230 |
rs751152296 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233518690 | CTTTGGATAATAGTG[C/T]GAGAGTTTCTTATAA | 55230 |
rs751172140 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233545874 | GATAATGGTAGTAAA[A/G]AGACAAGCACAGTGT | 55230 |
rs751235271 | in-del | -/ATTA | 5.78687e-05 | 0.00537875 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233559823 | ACCTCATTACTGGTC[-/ATTA]CACCCAAAGCTGTCA | 55230 |
rs751243080 | snp | A/G | 2.67098e-05 | 0.00365434 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233559897 | GCTGAGCAAACAAGC[A/G]CTGTAACTGTAAAGG | 55230 |
rs751257095 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233510922 | TCATAGCCCTGCTTT[C/T]CCTTTCTAACTCAAC | 55230 |
rs751269806 | snp | A/G | 3.3129e-05 | 0.00406982 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523236 | CCTTGCTCCCTGAAC[A/G]TCTTCCTCATGTCTT | 55230 |
rs751274839 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233536311 | CAACTAAAAAGTATA[A/G]TATCTGAAACGTATA | 55230 |
rs751310922 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233504704 | CAGAACACCCAAATA[C/T]ATAAAGCTAATATTA | 55230 |
rs751327556 | snp | C/T | | | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233491181 | CCTGAGACTTCAGCT[C/T]CGCCAGCGTGGCATC | 55230 |
rs751330498 | snp | C/T | 1.65693e-05 | 0.00287826 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233540707 | CTTCTTGTTCCAAGA[C/T]ATTCCTATCTTTTTC | 55230 |
rs751348785 | snp | G/T | 2.28626e-05 | 0.00338095 | intron-variant | USP40 | GRCh38.p7 | 2:233556826 | AATTTACAACATAAC[G/T]TATTACTAAAATACT | 55230 |
rs751401472 | snp | A/T | 3.10496e-05 | 0.00394003 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233512630 | GTTGTCAGCTATATA[A/T]AAAAGGAATATTATT | 55230 |
rs751454796 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233547406 | CTGATAGAATGTCAG[-/A]AATACAGACGAACAC | 55230 |
rs751505656 | snp | A/T | 2.79826e-05 | 0.00374039 | intron-variant | USP40 | GRCh38.p7 | 2:233511807 | CCGGCACTTAAAAAA[A/T]TTTTGATAATATGAT | 55230 |
rs751519604 | snp | A/G/T | 3.99243e-05 | 0.00446776 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477355 | TTGTGGCATCAGCCG[A/G/T]AGAGTTCATCGGGAG | 55230 |
rs751526572 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233521522 | ACAAAAGGGCCACAT[C/T]TAAGGAGTGTCACAC | 55230 |
rs751526585 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233484949 | GGGAATCCTTACTTT[G/T]GGTCCCACTTTAATG | 55230 |
rs751561332 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233552509 | GTATATTTAAAAACT[G/T]CATTTGTTTAGCAAA | 55230 |
rs751561552 | snp | C/T | 4.52478e-05 | 0.00475625 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485962 | CACCTGTGTCCTCAG[C/T]AGCACGTCCTGGGGG | 55230 |
rs751567564 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233503272 | AGAAAGCCTACAGGA[C/T]CAACAAGACACCATT | 55230 |
rs751568956 | snp | A/T | 3.43283e-05 | 0.00414282 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233549162 | TGGTAATGGCCTCCG[A/T]AGCAGCCACCTTTGT | 55230 |
rs751589732 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233515990 | GAAAGTCAATGACTA[C/T]GCACCTATTTCTAGA | 55230 |
rs751600280 | snp | C/T | 1.72743e-05 | 0.00293885 | intron-variant | USP40 | GRCh38.p7 | 2:233527376 | AGATGGTGCTCGATG[C/T]CTGAATTAAGAGGAA | 55230 |
rs751617183 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233566772 | TTGGCGAGGGCGGGT[C/G]TCCAGAAAGTGATTT | 55230 |
rs751647793 | snp | A/C | 1.65721e-05 | 0.0028785 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233540680 | CCGCAGTGGTCCATG[A/C]TGTTTTCTGTACTTC | 55230 |
rs751667534 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233549507 | ACTTTGGCTAAGATC[A/G]TGTAAGCCAATAAAA | 55230 |
rs751668660 | snp | A/C | 1.98971e-05 | 0.00315407 | intron-variant | USP40 | GRCh38.p7 | 2:233523501 | CAACCTGCAATCATA[A/C]CAAGACAACCATTAG | 55230 |
rs751699917 | snp | G/T | 1.71631e-05 | 0.00292938 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485593 | GCAAATAATCTTGTT[G/T]TTTTTTCTTTTTCCT | 55230 |
rs751708276 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233528129 | GATTACATGTGTGTG[A/C]CACCATGCCTGGCTA | 55230 |
rs751708827 | snp | C/T | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486895 | GGACAGAAAGGGCAT[C/T]GGCACAGATGCTGAA | 55230 |
rs751755468 | in-del | -/TTAAG | | | intron-variant | USP40 | GRCh38.p7 | 2:233526057 | CCATGGCTTTGCTCT[-/TTAAG]TTTCTAGATCTGAGA | 55230 |
rs751760799 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233482904 | TGCAGCTCCCTGCAA[C/T]TGGCAAGCTGATTCT | 55230 |
rs751773089 | snp | G/T | 1.69017e-05 | 0.00290699 | intron-variant | USP40 | GRCh38.p7 | 2:233493392 | ACTTCTCTTTATGAT[G/T]CACTGGCTGCTGAAA | 55230 |
rs751785601 | snp | A/C | 2.36309e-05 | 0.00343728 | intron-variant | USP40 | GRCh38.p7 | 2:233491267 | CCAGAAGCACCTTCC[A/C]AAGGACAGAGCGGGA | 55230 |
rs751801953 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233507526 | TGTTATTTGTGACAA[C/T]ATGGATGAACCTGGA | 55230 |
rs751808844 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233490961 | AGCACAGCATGCCTG[A/T]CAGAGGAGGGACCAG | 55230 |
rs751821802 | snp | G/T | 1.66738e-05 | 0.00288732 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533677 | AAATTTGCTGGTCAT[G/T]CCTTTGGAAATCAGA | 55230 |
rs751824374 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233514918 | TGCAGCCAATCCCTC[C/T]TCCTCCCTCCCAATC | 55230 |
rs751825828 | snp | C/T | 6.62855e-05 | 0.00575659 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556925 | CCATGGTACAGACGA[C/T]AGATGAGGTCATGAC | 55230 |
rs751833866 | in-del | -/ATC | 1.70304e-05 | 0.00291803 | cds-indel, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523175 | AGCGAGTTACCTGTT[-/ATC]ATCATGAGAATCCTG | 55230 |
rs751861260 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233493389 | TTTACTTCTCTTTAT[C/G]ATGCACTGGCTGCTG | 55230 |
rs751887136 | in-del | -/C | 0.00011629 | 0.00762441 | intron-variant | USP40 | GRCh38.p7 | 2:233510148 | CAACTAATAACAAGA[-/C]AGATGTGTAAATGCA | 55230 |
rs751944683 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233523913 | CCCCCTACTCCAGCA[C/T]GTATGGTGCAGTTCT | 55230 |
rs752019079 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233522574 | AAATATTGCAGTTAC[A/T]GTGTATGACACATTG | 55230 |
rs752052066 | snp | G/T | 1.66902e-05 | 0.00288874 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233524502 | TTTACCTCCACCCCA[G/T]TCCACACAAAGATGT | 55230 |
rs752089185 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233510271 | TTTATATGAAAATAC[A/G]ACTATGATTAATGTT | 55230 |
rs752144080 | snp | C/T | 1.65499e-05 | 0.00287657 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233559862 | TGCTGTGGATGCAGC[C/T]TCCTGGTCTAAGAGC | 55230 |
rs752169199 | snp | C/T | 1.98371e-05 | 0.00314931 | intron-variant | USP40 | GRCh38.p7 | 2:233499838 | TCAAAAAAATTTTTA[C/T]TAGGCTTTTAAGTAA | 55230 |
rs752218440 | snp | A/G | 1.78321e-05 | 0.00298593 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233493509 | CCCAGTGTCCTGAGG[A/G]ACCCTGAAGCTGGTA | 55230 |
rs752220545 | snp | C/T | 8.28397e-05 | 0.00643529 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523228 | TTCTGAGCCCTTGCT[C/T]CCTGAACGTCTTCCT | 55230 |
rs752235389 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233544834 | TTGCCTTGACCTTGA[C/T]ACTGGATGAAGGGGG | 55230 |
rs752269024 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233496090 | TGCAGAGAAAAGGTG[C/T]AGGAGTGATTTCTGC | 55230 |
rs752272267 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233483253 | CCAGCTCTTTGGGAG[C/G]CTGAGGCAGGTGAAC | 55230 |
rs752310606 | snp | C/T | 1.80624e-05 | 0.00300514 | intron-variant | USP40 | GRCh38.p7 | 2:233523131 | GTACTGTAATTAAAA[C/T]GACTTTTAGAAATCC | 55230 |
rs752367808 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233523750 | GGTGATGAAGCCAGA[C/T]TGGCCAAGGTCAGTT | 55230 |
rs752405139 | in-del | -/CTGT | | | intron-variant | USP40 | GRCh38.p7 | 2:233488900 | CGACAGAGCCAGACC[-/CTGT]CTATTAAGAAAAGAA | 55230 |
rs752407635 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233550958 | ACTTCTAATTTTGTT[C/T]TTAAATTTTCATTCC | 55230 |
rs752428095 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477302 | ATTTGGGATTGGAGG[C/T]GCCAGGCAGCCAGTC | 55230 |
rs752428382 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233518437 | CTGGGCGTGGTGGCA[C/T]ACGCCTGTAATCCCA | 55230 |
rs752446962 | snp | C/T | 0.000110485 | 0.00743171 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233529484 | ATTCAGTAAATGACA[C/T]GGAACCCCATATCTT | 55230 |
rs752462410 | snp | C/G | 0.000459797 | 0.0151554 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233489376 | CTACCTGAGTGGCTG[C/G]CGGTCAGTTCGTAAA | 55230 |
rs752464397 | snp | A/G | 1.92424e-05 | 0.00310175 | intron-variant | USP40 | GRCh38.p7 | 2:233477537 | TGTCATTGACTCATG[A/G]ATGCAGTGGGTGTCA | 55230 |
rs752511121 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233502552 | TGCCTCCCCAGAGAG[A/C]GCGCTGCACAGCTGC | 55230 |
rs752515125 | in-del | -/AA | 7.73007e-05 | 0.00621646 | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233561238 | AGTTCATATGGAACC[-/AA]AAAAGAGCCCGCATC | 55230 |
rs752519579 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233475863 | TTAAGAAGGGCTGGG[C/T]GCCCAGCTCGTCACG | 55230 |
rs752548153 | snp | A/G | 3.37166e-05 | 0.00410575 | intron-variant | USP40 | GRCh38.p7 | 2:233525612 | AAAAGTGACATATAC[A/G]TATCACCTTTCCAGG | 55230 |
rs752589460 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233531633 | CAGAAAAATACAAAG[C/G]CTTTTTCATTAACAG | 55230 |
rs752603552 | in-del | -/CTTTT | | | frameshift-variant, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233481235 | GGCCCGTTGTTTCTG[-/CTTTT]CTTTTCCAGTGTCAT | 55230 |
rs752607716 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476439 | AATCCTTTAAGTTGA[A/G]TAGAAATCTGGGTTG | 55230 |
rs752612994 | snp | A/G | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233487660 | AAAATATTTTCCTAC[A/G]GCGAAAAAAGAACAA | 55230 |
rs752633193 | snp | C/T | 1.65811e-05 | 0.00287929 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233525485 | TATCTTACCGCCAAG[C/T]GACTGGTAAATGTGA | 55230 |
rs752640045 | snp | C/T | 7.1286e-05 | 0.00596975 | intron-variant | USP40 | GRCh38.p7 | 2:233549084 | AAAGATATTTCTAAA[C/T]GAATTTCTATACGTA | 55230 |
rs752657318 | in-del | -/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233554166 | TGAGGTACAATAAAG[-/T]TTTCCCCGGAGAAAA | 55230 |
rs752659438 | snp | C/G | 0.000102606 | 0.00716188 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485889 | CGGCAGTCCCACCCT[C/G]GGCCGCGTTCCACAC | 55230 |
rs752699213 | snp | A/G | 3.32856e-05 | 0.00407942 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233496761 | GTAAAATCTTACCAG[A/G]GGAGGAAGTTGTCCT | 55230 |
rs752712044 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233528530 | AGACCTTAGTGCGGG[C/T]TGATGACAGCCCCTC | 55230 |
rs752725174 | snp | A/G | 0.000852878 | 0.0206328 | intron-variant | USP40 | GRCh38.p7 | 2:233559965 | AAATGAATTCTTTAA[A/G]TGTTGACTAAGGCTT | 55230 |
rs752765607 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233514531 | AGATCACAAGGTTAC[A/G]GTTAAGCAGGGGTCA | 55230 |
rs752781966 | in-del | -/G | | | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233512285 | AATTCACAAAAAAAT[-/G]GAAAAATTTTGAAAA | 55230 |
rs752789421 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233563315 | TTGGCAACCCCATGC[A/G]AGTCTCCAGAATTTC | 55230 |
rs752818948 | snp | A/G | 3.32392e-05 | 0.00407658 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533664 | GGAAGCATCTTGAAA[A/G]TTTGCTGGTCATTCC | 55230 |
rs752832733 | snp | C/T | 3.3162e-05 | 0.00407184 | intron-variant | USP40 | GRCh38.p7 | 2:233491143 | CACATTACCACTAAG[C/T]TATGGTGCAGGAAGA | 55230 |
rs752845828 | snp | A/G | 2.21693e-05 | 0.00332929 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233491248 | AACTTGCGCAGGCTC[A/G]TTCCCAGAAGCACCT | 55230 |
rs752848511 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233499307 | GGATAATGACTTCCA[C/G]CTCCATCCATGACCC | 55230 |
rs752871657 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233542850 | GAATACGAAACAAGT[A/T]AACCTTCTAGCACAA | 55230 |
rs752896968 | snp | A/T | 3.46404e-05 | 0.00416161 | intron-variant | USP40 | GRCh38.p7 | 2:233554553 | ATGAATATAATATTG[A/T]AAAACAATTTCAGAG | 55230 |
rs752935622 | snp | A/G | 8.36342e-05 | 0.00646607 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233512609 | ATCAATAGGTCTCAA[A/G]CAGCTGTTGTCAGCT | 55230 |
rs753020859 | in-del | -/C | 1.65616e-05 | 0.00287759 | frameshift-variant, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523290 | TCCCCACCTGGACAT[-/C]CAGCACTGTTGATGA | 55230 |
rs753025327 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233560451 | AGACTTTAAGTATTT[A/G]AAGGAGAATAAGCAT | 55230 |
rs753056737 | snp | G/T | 1.73724e-05 | 0.00294719 | intron-variant | USP40 | GRCh38.p7 | 2:233549243 | CTCTAAAAGAAAAAA[G/T]AACAAAAATATTGAT | 55230 |
rs753092666 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233548346 | GAAAGCTACAGACAC[A/G]GGATTTATTGTTTTT | 55230 |
rs753099337 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233522369 | TACAGTTCTTATAAA[C/G]AAGGTAGGGAATGTC | 55230 |
rs753117882 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233554758 | TATAAGAAAAGTTTA[C/T]GAATTTACCAAAGAT | 55230 |
rs753118678 | snp | A/G | | | intron-variant, missense | USP40 | GRCh38.p7 | 2:233487948 | TCCGAACACACTGAC[A/G]ACAGCTGCGGGTGGG | 55230 |
rs753130562 | snp | A/T | 1.99563e-05 | 0.00315876 | intron-variant | USP40 | GRCh38.p7 | 2:233499832 | AAAAAGTCAAAAAAA[A/T]TTTTATTAGGCTTTT | 55230 |
rs753171170 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233556725 | AGGTGTAGTTAGAAG[-/A]AAAAAAAAACTCAAT | 55230 |
rs753182502 | snp | A/T | 2.13186e-05 | 0.00326479 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533769 | AATATCTGAGAATGG[A/T]GCTGTAAGAACTACA | 55230 |
rs753216679 | snp | C/T | 1.85431e-05 | 0.00304486 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523483 | TTTGAATGTGGACTC[C/T]ACCAACCTGCAATCA | 55230 |
rs753218732 | snp | C/T | 1.6819e-05 | 0.00289987 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233498576 | GGCTCTCCAGCTTCA[C/T]AGCACCAATCCATTT | 55230 |
rs753266713 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233528573 | TTATTTTTTTATTTT[A/T]ATTTTTTTAAAATAA | 55230 |
rs753294564 | snp | A/T | 1.70423e-05 | 0.00291905 | intron-variant | USP40 | GRCh38.p7 | 2:233520984 | CCTTTAATTATATTC[A/T]ACTCACTGTGTTAAC | 55230 |
rs753308409 | snp | C/T | 1.65647e-05 | 0.00287786 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523398 | TCTATCACCTGACAA[C/T]ACTTTTCTCCATCAC | 55230 |
rs753309623 | in-del | -/T | 3.00368e-05 | 0.00387524 | frameshift-variant, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233512616 | GGTCTCAAACAGCTG[-/T]TGTCAGCTATATATA | 55230 |
rs753360146 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233510988 | ATGCACTACTATTTG[C/G]TACGGTTCAGGGGAA | 55230 |
rs753369353 | in-del | -/AT | 3.3123e-05 | 0.00406945 | frameshift-variant, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523373 | ATTAGCTGGAAAGAC[-/AT]GTGGAGATTCTATCA | 55230 |
rs753385172 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233522258 | CAGTGATTAACACTG[C/T]ATGCTGAGAAGACGG | 55230 |
rs753393037 | snp | A/G | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486664 | GAATGATTTTTAGAT[A/G]TACTTCTATTAAGTG | 55230 |
rs753409963 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233507677 | AACAGCAGTTACTAG[A/T]GACTGAGGGGGAGAT | 55230 |
rs753420527 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233492426 | GTGTACAGATGTATT[A/G]CCAAAAAAAGAACCT | 55230 |
rs753448053 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233521210 | TGACTAATTAGAGGT[A/G]ACCAAGTTCTACTGA | 55230 |
rs753494783 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233557309 | ACACACATGGCCATG[A/C]CACAGAAAGCAGAGA | 55230 |
rs753507631 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233513971 | TGAGTTCAATATCTT[C/G]TATTACAGTAATATG | 55230 |
rs753518746 | snp | C/T | 3.44382e-05 | 0.00414945 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233488287 | CAGATCTCAATTCTC[C/T]GTCCTAGTTTATATT | 55230 |
rs753520707 | in-del | -/TAA | | | intron-variant | USP40 | GRCh38.p7 | 2:233481314 | ACATTTCAAAAGAAG[-/TAA]TAATGAGCAGTGTTT | 55230 |
rs753537458 | snp | C/G | 1.72394e-05 | 0.00293589 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551378 | AAATAGTTCAAACCT[C/G]TTCACAAAAGGGCTT | 55230 |
rs753562879 | snp | C/T | 0.000116747 | 0.00763938 | intron-variant | USP40 | GRCh38.p7 | 2:233542231 | CATACACACAATACA[C/T]ACCATACATACAAAT | 55230 |
rs753562911 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233530548 | TTCAAGGCTTTTAAA[C/T]ACACATACTCAAACT | 55230 |
rs753622689 | snp | A/C | 2.53309e-05 | 0.00355876 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485886 | AGCCGGCAGTCCCAC[A/C]CTGGGCCGCGTTCCA | 55230 |
rs753663117 | snp | A/G | 1.67172e-05 | 0.00289108 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233524548 | TTTCAGTTTCACACA[A/G]TGTCAGTTCATCCCC | 55230 |
rs753670648 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233483076 | GTTACTGCGTATGTC[A/G]CTCCCCTGTTTGTGA | 55230 |
rs753693410 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233483803 | CAGTTCTGGTCCCAA[C/G]CATCTTGAATCATAG | 55230 |
rs753733517 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233539255 | GAAACAAAGAACACA[A/C]TCAATTTGACCTAGT | 55230 |
rs753762934 | snp | C/T | 2.52325e-05 | 0.00355184 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233559847 | GCTGTCAGTGAGGTC[C/T]GCTGTGGATGCAGCT | 55230 |
rs753780819 | snp | C/T | 1.66921e-05 | 0.00288891 | intron-variant | USP40 | GRCh38.p7 | 2:233493413 | GCTGCTGAAATCCCA[C/T]TCTGTTCTCACCTTG | 55230 |
rs753781280 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556859 | GGCATATTTACCTGC[C/T]TCTCGCTAACGTTCT | 55230 |
rs753786759 | snp | C/T | 1.77055e-05 | 0.00297531 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233493504 | ACTCTCCCAGTGTCC[C/T]GAGGGACCCTGAAGC | 55230 |
rs753820031 | in-del | -/A | 1.65553e-05 | 0.00287705 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485730 | CATTGCTATGCCGGT[-/A]AGCCCCAATTTCTCT | 55230 |
rs753849251 | snp | C/T | 4.99646e-05 | 0.00499798 | intron-variant | USP40 | GRCh38.p7 | 2:233557039 | AAAACAGGTAACTTT[C/T]AGATGTAATTCCGGG | 55230 |
rs753929486 | snp | A/T | 2.30332e-05 | 0.00339354 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233511786 | CTTCCTTCAAAGTAT[A/T]GCTGTCCGGCACTTA | 55230 |
rs753931401 | snp | C/T | 0.000205712 | 0.0101397 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233489418 | GCGCTTCCTCTCCAC[C/T]GTCCAGGCTCTGAGG | 55230 |
rs753943057 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233479630 | GTATAGAATTTTACG[C/T]GTGTGTGTGTGTGTG | 55230 |
rs753957797 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233538758 | GTGGTGGCTCATGCC[C/T]ATAATCCCAGCACTT | 55230 |
rs754003874 | in-del | -/GTGT | | | intron-variant | USP40 | GRCh38.p7 | 2:233491606 | CAACCTGTTCCTCGT[-/GTGT]GTGTGTGTGTGTGTG | 55230 |
rs754042049 | snp | C/T | 0.000114019 | 0.00754959 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233565462 | TTCTCTAGGAGCAGG[C/T]GGCTCCAAAGCTTTA | 55230 |
rs754102061 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233504657 | ATTCAATGAGAGGAT[A/G]TAACAATTGTAAATA | 55230 |
rs754106568 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233549894 | CTCCATAATCATGAG[C/T]GATCAAACAGATGTA | 55230 |
rs754166762 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233500158 | AGCAGGACTTAGTTC[A/C]AAGTTTCATCCACCA | 55230 |
rs754183882 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233533174 | CAAGTCTGAGCATAT[A/G]GCAATCGCACTCAAG | 55230 |
rs754183933 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233548176 | TGGAAAAAAATCCTT[C/T]TTACACCTCTCATAG | 55230 |
rs754243970 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233560294 | TGTAGAAATTTTCCA[A/G]GCACAATACTGTATC | 55230 |
rs754347012 | snp | A/G | 1.65891e-05 | 0.00287998 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533639 | ATTGTTTAAACCTGG[A/G]GATTCTGGAGGAAGC | 55230 |
rs754350322 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233497794 | GCCCAGGCCCCAAGA[A/G]GGGCCTCTTGCTATT | 55230 |
rs754352365 | snp | A/C | 6.86919e-05 | 0.00586014 | intron-variant | USP40 | GRCh38.p7 | 2:233554542 | CTGAAATAGACATGA[A/C]TATAATATTGAAAAA | 55230 |
rs754395368 | in-del | -/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233524687 | TTTAAAAAGTAGTAA[-/T]TTATTTTTATTCTAT | 55230 |
rs754405883 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233507770 | AGCTCTAGTGTTCTA[C/T]TGTACAGTAGGGTGA | 55230 |
rs754412674 | snp | C/T | 0.00010605 | 0.00728106 | intron-variant | USP40 | GRCh38.p7 | 2:233491078 | CAGAACAGACTGTAA[C/T]TGAGGGAAAAGGAGA | 55230 |
rs754418560 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233513371 | GTAAAATGTCATGGT[A/G]GGTTTAGCACTACAA | 55230 |
rs754434921 | snp | C/T | 1.65781e-05 | 0.00287902 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533534 | CATGTAGGCACTTTC[C/T]TTACCCTGAAATTGC | 55230 |
rs754437887 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233563190 | TAACAAACATCCTTT[C/T]GTGGGAAGGATCCTC | 55230 |
rs754455200 | in-del | -/TAAGT | 1.75164e-05 | 0.00295937 | intron-variant | USP40 | GRCh38.p7 | 2:233533806 | CAAAAAAAAAAATGC[-/TAAGT]TAATTATTTAAACAA | 55230 |
rs754492955 | snp | G/T | 1.66735e-05 | 0.00288729 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233493426 | CATTCTGTTCTCACC[G/T]TGGCTGGAAGTGGCT | 55230 |
rs754496030 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233492479 | ACATACTGATTAAAC[A/G]TGCTTTTACAATCTA | 55230 |
rs754500108 | snp | C/T | 1.66687e-05 | 0.00288688 | intron-variant | USP40 | GRCh38.p7 | 2:233557043 | CAGGTAACTTTTAGA[C/T]GTAATTCCGGGCTTC | 55230 |
rs754550562 | snp | C/T | 1.70139e-05 | 0.00291662 | intron-variant | USP40 | GRCh38.p7 | 2:233520986 | TTTAATTATATTCTA[C/T]TCACTGTGTTAACAG | 55230 |
rs754558810 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477310 | TTGGAGGCGCCAGGC[A/G]GCCAGTCCCCATGCC | 55230 |
rs754565757 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233532944 | TAAAAATAAATAAAT[A/G]AATAAATAAACAAAA | 55230 |
rs754584208 | snp | C/T | 3.31329e-05 | 0.00407005 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556941 | AGATGAGGTCATGAC[C/T]GGAGGTCCCAACTAA | 55230 |
rs754611142 | snp | C/T | 0.000112292 | 0.00749223 | intron-variant | USP40 | GRCh38.p7 | 2:233477522 | CAGAGACACAGACAC[C/T]GTCATTGACTCATGG | 55230 |
rs754618929 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233536354 | GTCTTAACAGAAGAG[G/T]GGCTCAGTGGAAGAA | 55230 |
rs754626077 | in-del | -/TCGTACCTCATTACTGG | 5.72525e-05 | 0.00535004 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233559824 | CCTCATTACTGGTCC[-/TCGTACCTCATTACTGG]ACCCAAAGCTGTCAG | 55230 |
rs754640028 | snp | C/T | 1.90911e-05 | 0.00308953 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527568 | TATTGTTTGCAGAAT[C/T]ACATTCTGCCCTTTA | 55230 |
rs754672206 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233506674 | CCGAGATGGGCAGAT[C/T]ACTTGAGTTCAGTAG | 55230 |
rs754716154 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233546564 | GGGAGCACTTCCTAA[G/T]ACTGAAGAGAGACAC | 55230 |
rs754721445 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233477975 | TCGCTGTGACCCCCC[C/T]GGCCCATGGCACCGT | 55230 |
rs754723098 | in-del | -/AG | | | intron-variant | USP40 | GRCh38.p7 | 2:233481146 | TTCCAAGCAGGAATA[-/AG]AGAGAGTCAGAGAGG | 55230 |
rs754734439 | snp | A/C | 1.65828e-05 | 0.00287943 | intron-variant | USP40 | GRCh38.p7 | 2:233499962 | TTCTGTTTCTGAGTT[A/C]CAGTTCTAGGACAAA | 55230 |
rs754750733 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233515501 | CTTACTGGTCATTCA[C/T]AGGTACGTCTTCTTT | 55230 |
rs754780034 | in-del | -/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233478163 | GAAGCTGCCTTGTAA[-/T]TTTGGGGATATCCTG | 55230 |
rs754787699 | snp | C/T | 3.35048e-05 | 0.00409283 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233524555 | TTCACACAGTGTCAG[C/T]TCATCCCCTAGAAAG | 55230 |
rs754799860 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233516363 | TGTAAGAATATATTA[A/C]ATCTACACATCAAAT | 55230 |
rs754805621 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233518172 | GTACCCCAATAACCT[A/G]TGGAAAAAATAACAA | 55230 |
rs754816736 | snp | A/G | 9.43049e-05 | 0.00686612 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485833 | TTCAATCTTCTCCAC[A/G]GGAAGACGATAGAAA | 55230 |
rs754822184 | in-del | -/TC | 3.06866e-05 | 0.00391693 | frameshift-variant, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233549131 | CCCAAATGATCAACA[-/TC]TCTTTAATATATACA | 55230 |
rs754851177 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233493925 | ATCACACAGATGCAA[C/G]AGCCCATTGATCTAA | 55230 |
rs754856990 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233484962 | TTGGGTCCCACTTTA[A/T]TGAAAATGGAAGCTT | 55230 |
rs754871539 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233529073 | ACAACTACTTACCTA[C/T]GAGGGGTGATTTTCA | 55230 |
rs754885851 | snp | C/T | 1.65693e-05 | 0.00287826 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233540715 | TCCAAGATATTCCTA[C/T]CTTTTTCAAAAGTTT | 55230 |
rs754886757 | snp | C/T | 1.78169e-05 | 0.00298465 | intron-variant | USP40 | GRCh38.p7 | 2:233542246 | TACCATACATACAAA[C/T]ACATACACACACATA | 55230 |
rs754906656 | snp | A/G | 3.54277e-05 | 0.00420863 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233493505 | CTCTCCCAGTGTCCT[A/G]AGGGACCCTGAAGCT | 55230 |
rs754964863 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233558835 | ATTAACGCCAAATAC[C/G]AGCCCTACACCAGAA | 55230 |
rs754994716 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233480686 | ATGGCCTGTGGCAGC[A/G]GAGTCCTGGCGGCCA | 55230 |
rs755003510 | snp | A/C | 3.05694e-05 | 0.00390944 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233481266 | TCATCTCTGATTGTA[A/C]TGAAATCATCATCGT | 55230 |
rs755041857 | snp | C/T | 8.72867e-05 | 0.00660573 | intron-variant | USP40 | GRCh38.p7 | 2:233491113 | AGAATATATTAATAT[C/T]TCACTGGAAGAAGCC | 55230 |
rs755054772 | snp | A/G | 3.31647e-05 | 0.00407201 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233554459 | TCCTCTTCTACATAC[A/G]TGTTCCAGAGAGCAT | 55230 |
rs755067653 | snp | C/T | 3.31543e-05 | 0.00407137 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533536 | TGTAGGCACTTTCTT[C/T]ACCCTGAAATTGCTG | 55230 |
rs755121200 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233528437 | CTGACCAATGTGGAG[C/G]TGGAATGAGGCTTAT | 55230 |
rs755149115 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233511481 | ACTCAGCATCAAAGA[C/T]TCCTTTTAACCACAA | 55230 |
rs755155473 | snp | C/G/T | 0.000158168 | 0.00889179 | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233529560 | GCTAAATGAAATCTG[C/G/T]TTGCTGGAAGAGGTA | 55230 |
rs755215889 | snp | A/C/G | 0.00014126 | 0.00840314 | missense, synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233510129 | CCATTGCAAAAAACA[A/C/G]GAACAACTAATAACA | 55230 |
rs755248560 | in-del | -/CTGA | | | intron-variant | USP40 | GRCh38.p7 | 2:233553836 | TCAGTTGCTTCAGTC[-/CTGA]CTGACTTTCTTTTGT | 55230 |
rs755264556 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233491022 | GCGTGTATTGCCTGC[A/G]GGTACTTACCACTGA | 55230 |
rs755297616 | snp | A/C | 3.11716e-05 | 0.00394776 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233549105 | TCTATACGTACTTGA[A/C]ACTGCCAGTTTCCCA | 55230 |
rs755360547 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233534612 | AGTATTATTTTATCA[A/G]CAAACAGAAGAGTGT | 55230 |
rs755362193 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233507534 | GTGACAACATGGATG[A/T]ACCTGGAAGACATCA | 55230 |
rs755402222 | in-del | -/A | 0.000225851 | 0.0106242 | frameshift-variant, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233491255 | CAGGCTCGTTCCCAG[-/A]AAGCACCTTCCAAAG | 55230 |
rs755417256 | in-del | -/AAA | 2.66535e-05 | 0.00365049 | intron-variant | USP40 | GRCh38.p7 | 2:233511801 | AGCTGTCCGGCACTT[-/AAA]AAAATTTTGATAATA | 55230 |
rs755434084 | snp | A/C | 1.66125e-05 | 0.00288201 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233496789 | CCTTCAATTAAAAGC[A/C]AAGTATCTCCAGAAC | 55230 |
rs755468867 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233547212 | ATATATTTTGGTATA[C/T]AAAATCAACATACTA | 55230 |
rs755480062 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233548235 | AAATGTAATTCAATC[A/G]GTGGTTATTGAGCAC | 55230 |
rs755519580 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233533216 | AAGAAGGTTTTATGC[C/T]ATCCAAGGAAATCCA | 55230 |
rs755521870 | snp | A/G | 1.84272e-05 | 0.00303534 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485501 | CCTCGTGTCTTCTCA[A/G]AGTGGTAAATTTGCT | 55230 |
rs755528136 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233497892 | CCTTCTGCTGGCATT[C/G]AGTGCCCCTTCTTAA | 55230 |
rs755545386 | in-del | -/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233530632 | AGAGTCACAGAAATA[-/G]TATCTGATTTGGTGG | 55230 |
rs755555046 | snp | A/G | 3.31901e-05 | 0.00407356 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533649 | CCTGGGGATTCTGGA[A/G]GAAGCATCTTGAAAA | 55230 |
rs755588227 | snp | A/T | 5.48531e-05 | 0.00523675 | intron-variant | USP40 | GRCh38.p7 | 2:233556850 | AAATACTCTGGCATA[A/T]TTACCTGCCTCTCGC | 55230 |
rs755613648 | snp | C/T | 3.37012e-05 | 0.00410481 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477436 | GAGAAGTTTCCGGGG[C/T]TCGGGGCCGGGCAGG | 55230 |
rs755618265 | snp | C/G | 0.000167182 | 0.00914129 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233512655 | ATTATTTTTCTTAGA[C/G]AGCTAGGAATTAATA | 55230 |
rs755701591 | snp | A/G | 3.4379e-05 | 0.00414588 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477388 | GAGCCGTGCAGCGGC[A/G]CGGTTATCTGAAGCT | 55230 |
rs755706103 | snp | C/T | 1.67548e-05 | 0.00289432 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527490 | CTGTTTGAGAGACTA[C/T]TGGGTGCAGAGCCCC | 55230 |
rs755721204 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233518821 | TTCATAGTGGCATTA[C/T]TCATAAAAGCACAAA | 55230 |
rs755723334 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233505021 | TTTTTTCTAACCACG[A/G]TAAAACTAGAAATCA | 55230 |
rs755738794 | snp | A/G | 0.000108278 | 0.00735712 | intron-variant | USP40 | GRCh38.p7 | 2:233488055 | TGTTTTTATGGGAGA[A/G]TAAGTCCCAAGTTTT | 55230 |
rs755774596 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233479120 | CCATGAATTTTTAAA[A/T]TGTGCTATCTCAAAC | 55230 |
rs755779269 | snp | C/T | 4.61542e-05 | 0.00480364 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233549225 | TCTAAGTCATCCAAT[C/T]CACTCTAAAAGAAAA | 55230 |
rs755828415 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476726 | TGCGGGCTGACGTGC[A/G]GCGGCTGCCCTTGCT | 55230 |
rs755851816 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233522428 | GTGGTAAGTGTACTA[C/T]GAAAGAAACGGTCCA | 55230 |
rs755861330 | snp | A/G | 2.10042e-05 | 0.00324063 | intron-variant | USP40 | GRCh38.p7 | 2:233523516 | CCAAGACAACCATTA[A/G]TACAGCTGATATTTG | 55230 |
rs755891297 | snp | A/G | 1.65696e-05 | 0.00287828 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233540705 | TACTTCTTGTTCCAA[A/G]ATATTCCTATCTTTT | 55230 |
rs755905369 | snp | A/G | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233487680 | AAAAAGAACAAGATG[A/G]TTTGATTGTAGACAA | 55230 |
rs755980721 | snp | A/T | 1.66128e-05 | 0.00288204 | intron-variant | USP40 | GRCh38.p7 | 2:233557025 | GCCTCATTTCCTACA[A/T]AACAGGTAACTTTTA | 55230 |
rs755997224 | snp | A/G | 1.65688e-05 | 0.00287821 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556932 | ACAGACGATAGATGA[A/G]GTCATGACCGGAGGT | 55230 |
rs756008896 | in-del | -/ATA | 0.0331383 | 0.124383 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562711 | CCTAAAACTTAAAGT[-/ATA]ATAATAATAATAATA | 55230 |
rs756009701 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233480947 | GGAGGGGGACCGGGG[G/T]GCCATGGATCTGCGG | 55230 |
rs756025990 | snp | A/G | 1.72305e-05 | 0.00293513 | intron-variant | USP40 | GRCh38.p7 | 2:233520967 | GAAAATCTATCAGCC[A/G]ACCTTTAATTATATT | 55230 |
rs756045236 | snp | C/G | 1.74842e-05 | 0.00295665 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485606 | TTTTTTTTTCTTTTT[C/G]CTCTTGGTTATTTGT | 55230 |
rs756046963 | snp | C/T | 0.000116929 | 0.00764531 | intron-variant | USP40 | GRCh38.p7 | 2:233493409 | ACTGGCTGCTGAAAT[C/T]CCATTCTGTTCTCAC | 55230 |
rs756090889 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233527674 | CTTACAATAAAGTTC[C/T]CCATCCCACCAAAGT | 55230 |
rs756095990 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233479043 | TGTTCAGAAGACACC[A/G]GTGGTCTACTGTTGT | 55230 |
rs756103290 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233491358 | TTGTAAATAGGTTAT[C/T]AAAATTCCACTCAAG | 55230 |
rs756105235 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233506494 | AGGCAACAAAAGAAC[A/G]TAGACAAATGGGATT | 55230 |
rs756140845 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233495894 | AAGGTAGGTGTGTAT[A/G]TGCTGATATGAGGAG | 55230 |
rs756163949 | snp | C/G | 3.40096e-05 | 0.00412354 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233510114 | GTTGAACGTCACTCC[C/G]CATTGCAAAAAACAG | 55230 |
rs756167320 | snp | A/G | 5.39389e-05 | 0.00519293 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233489378 | ACCTGAGTGGCTGCC[A/G]GTCAGTTCGTAAAAG | 55230 |
rs756200333 | snp | A/C | 0.000113954 | 0.00754744 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233565414 | GAGGTAACAGGTTCC[A/C]CCCTGATTTCTGATT | 55230 |
rs756227680 | snp | A/G | 1.65707e-05 | 0.00287838 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551494 | GAAACAGTAAGAAAA[A/G]GAGGCAGCTTACGTA | 55230 |
rs756253816 | snp | A/C | 1.88198e-05 | 0.0030675 | intron-variant | USP40 | GRCh38.p7 | 2:233499958 | AGTTTTCTGTTTCTG[A/C]GTTACAGTTCTAGGA | 55230 |
rs756254656 | in-del | -/AGCTGC/AGCTGCCTT/AGCTGCCTTCCCCTGCTTTGCA/AGCTGCCTTCCCCTGCTTTGCACTGGCAGCA/AGCTGCCTTCCCCTGCTTTGCACTGGCAGCACGGCATGGTT | 0.000212912 | 0.0103161 | intron-variant | USP40 | GRCh38.p7 | 2:233477540 | ATTGACTCATGGATG[lengthTooLong]CAGTGGGTGTCAGGG | 55230 |
rs756277901 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233550941 | TTCTAAATGCAGGGT[A/G]AACTTCTAATTTTGT | 55230 |
rs756287246 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233524370 | CCTGACCTCAGGTGA[A/T]CTGCCTGCCTCGCCC | 55230 |
rs756299327 | snp | C/T | 3.44329e-05 | 0.00414913 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551415 | AATCCGGAGAGGGAA[C/T]GTATAACAGCTAGTT | 55230 |
rs756313417 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233501506 | AAGTGCAAGGCTATA[A/G]GGAAGGAGATCAGTT | 55230 |
rs756342903 | in-del | -/AA | | | intron-variant | USP40 | GRCh38.p7 | 2:233512729 | TCAAACACAGAAAAC[-/AA]AAGAGAGATGCTCTA | 55230 |
rs756343092 | snp | A/G | 8.85779e-05 | 0.0066544 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233561271 | CCAAGTCAATCCTAA[A/G]CCAAAAGAACAAAGC | 55230 |
rs756392271 | snp | A/G | 2.72327e-05 | 0.00368994 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233559902 | GCAAACAAGCGCTGT[A/G]ACTGTAAAGGGATGA | 55230 |
rs756395317 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233537075 | TTTTTGTACAGATGG[A/G]GTCTTGCTATGTTGC | 55230 |
rs756431897 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233546206 | GGGAAGAGATCCTGA[G/T]GCTGCTAGAAAGAAG | 55230 |
rs756448211 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233554865 | GGTATACAGTACTGT[C/T]TTAGACTAGACTATA | 55230 |
rs756448654 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233538493 | GAAATGAAAAAGGAA[C/T]CATAAGTTCATATTC | 55230 |
rs756486836 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233546965 | AACTTCCTCTAATTG[A/G]GAAGGTGCCCGGCAA | 55230 |
rs756501058 | snp | A/G | | | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556970 | AAAGAAGTTTCCAAA[A/G]CGCTGAAGAGGATTC | 55230 |
rs756517379 | in-del | -/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233528882 | GAGTCAAAGGTGAGG[-/C]CCCAAAAGAGAATGC | 55230 |
rs756546601 | in-del | -/AGTC | | | intron-variant | USP40 | GRCh38.p7 | 2:233481152 | GCAGGAATAAGAGAG[-/AGTC]AGAGAGGGCTCTGTC | 55230 |
rs756557377 | snp | A/T | 3.59124e-05 | 0.00423733 | intron-variant | USP40 | GRCh38.p7 | 2:233523144 | AATGACTTTTAGAAA[A/T]CCTTTTTCTCTTGTT | 55230 |
rs756582280 | snp | G/T | 5.77734e-05 | 0.00537432 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233481239 | CGTTGTTTCTGCTTT[G/T]CTTTTCCAGTGTCAT | 55230 |
rs756590701 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233511280 | AAGTCTAAAATTAAT[A/C]AACTGTGTTTCATTC | 55230 |
rs756598303 | in-del | -/AAAGACATGTGGAGATTCT | 1.65616e-05 | 0.00287759 | frameshift-variant, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523367 | TTCTGCATTAGCTGG[-/AAAGACATGTGGAGATTCT]ATCACCTGACAACAC | 55230 |
rs756607277 | snp | A/G | 2.01351e-05 | 0.00317288 | intron-variant | USP40 | GRCh38.p7 | 2:233477552 | GATGCAGTGGGTGTC[A/G]GGGTGAGGGGTTCAC | 55230 |
rs756610620 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233479495 | TTGAACCCGGGAGGC[A/G]GAGGTTGAAGTGGGT | 55230 |
rs756738408 | snp | C/T | | | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233566884 | TCTGCTCCAAGAGTT[C/T]GGGAACTGGAGCGGG | 55230 |
rs756742327 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476031 | GGGCGCAGTGCTTCA[C/T]GGAAACGCACAGACG | 55230 |
rs756759743 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233514225 | TCTAATGGGGGAGGT[A/G]GATATTAAAAACACA | 55230 |
rs756822883 | in-del | -/TATT | 0.000132886 | 0.00815017 | intron-variant | USP40 | GRCh38.p7 | 2:233540655 | CAAAACGATGCCATG[-/TATT]TATTACCTTCCGCAG | 55230 |
rs756855563 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233518708 | GAGTTTCTTATAAAG[C/T]TAAACATAAATTTGC | 55230 |
rs756877809 | in-del | -/T | 0.000273806 | 0.0116974 | intron-variant | USP40 | GRCh38.p7 | 2:233524482 | ATATTTCTTCAGTAA[-/T]TTTTTTTACCTCCAC | 55230 |
rs756930431 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233546015 | AAAAAAAAATAACAA[A/C]TGGGATGCTTGATAG | 55230 |
rs756998972 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233490555 | CCACTAGTCATATAT[A/G]GGCCCCACATTTTCT | 55230 |
rs757009672 | snp | C/T | 1.67128e-05 | 0.00289069 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533682 | TGCTGGTCATTCCTT[C/T]GGAAATCAGACTCAG | 55230 |
rs757033689 | in-del | -/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233549401 | ATTTTTAAATTAATT[-/G]GATCTAATGGCCAGT | 55230 |
rs757081395 | snp | C/T | 4.50958e-05 | 0.00474825 | intron-variant | USP40 | GRCh38.p7 | 2:233556829 | TTACAACATAACTTA[C/T]TACTAAAATACTCTG | 55230 |
rs757085224 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233495714 | GCCTGTCGGGGAGAG[A/G]ACACTGGGTGGCTGG | 55230 |
rs757096053 | snp | C/G | 0.000436639 | 0.0147692 | intron-variant | USP40 | GRCh38.p7 | 2:233491270 | GAAGCACCTTCCAAA[C/G]GACAGAGCGGGATGT | 55230 |
rs757109334 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476573 | CTGGGCTATGCCAGG[A/C]CTGTCTGCCACAGCC | 55230 |
rs757152404 | snp | C/G | 6.69467e-05 | 0.00578523 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527471 | GTCAAATCCCACACG[C/G]TTTCTGTTTGAGAGA | 55230 |
rs757155866 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233539565 | TAGAAAATATTTCAA[A/T]CTGAATGAAAATGAA | 55230 |
rs757181909 | snp | G/T | 0.000108648 | 0.00736969 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233512651 | GAATATTATTTTTCT[G/T]AGAGAGCTAGGAATT | 55230 |
rs757182833 | in-del | -/AAAGAAAGAAACGAG | | | intron-variant | USP40 | GRCh38.p7 | 2:233488945 | GAAAGGAAAGAAAGA[-/AAAGAAAGAAACGAG]AAAGAAAGAAACAAA | 55230 |
rs757222528 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233554143 | AAGGAGGGATACTTA[C/G]GAAACACTGAGGTAC | 55230 |
rs757242075 | snp | C/T | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486985 | GAGAGCAGGAGTGCC[C/T]TGGAAGTTGGTCAAG | 55230 |
rs757264675 | snp | G/T | 1.94831e-05 | 0.00312109 | intron-variant | USP40 | GRCh38.p7 | 2:233499846 | ATTTTTATTAGGCTT[G/T]TAAGTAATATGTCAT | 55230 |
rs757271913 | snp | G/T | 6.32992e-05 | 0.00562544 | intron-variant | USP40 | GRCh38.p7 | 2:233511819 | AAAATTTTGATAATA[G/T]GATGAAGGTTATTAA | 55230 |
rs757317450 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233501293 | AGTGAGTAAGAGGGG[C/G]AAATGGTTGGAGGTT | 55230 |
rs757350104 | snp | A/C | 3.98589e-05 | 0.00446406 | intron-variant | USP40 | GRCh38.p7 | 2:233523502 | AACCTGCAATCATAC[A/C]AAGACAACCATTAGT | 55230 |
rs757360045 | snp | C/G | 1.90311e-05 | 0.00308467 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485753 | ATTTCTCTGAGACAG[C/G]CCCACAACTTTACCC | 55230 |
rs757367572 | snp | C/G | 8.74088e-05 | 0.00661035 | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233561260 | AGCCCGCATCGCCAA[C/G]TCAATCCTAAGCCAA | 55230 |
rs757381889 | in-del | -/CTT | | | intron-variant | USP40 | GRCh38.p7 | 2:233563297 | GCATGGGGTTGCCAA[-/CTT]CTTTTTCCAGATAAG | 55230 |
rs757386363 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233482947 | TTCCTGGCCATTCTC[C/T]TCTCCTCTGTGAACT | 55230 |
rs757397104 | in-del | -/T | 3.74848e-05 | 0.00432909 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485762 | AGACAGCCCCACAAC[-/T]TTACCCAGCTAGATA | 55230 |
rs757406761 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233564389 | AGGGCCAGGTGAAGG[C/T]AAAGTAATGTTCACA | 55230 |
rs757407919 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233514975 | TAGATTTTATTTGTC[C/T]AAAGTGTCCTATGTA | 55230 |
rs757429415 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233500360 | GAATTTCCCCGTTTT[C/T]CCTAAATATAAAAAC | 55230 |
rs757456036 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233534887 | TCCCATTAATGACAA[A/T]GAAATTTTCTTAGAC | 55230 |
rs757461256 | snp | C/T | 6.446e-05 | 0.00567678 | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233561190 | ATCCTTATCTTCAAA[C/T]AAACCAAGCTCTTCT | 55230 |
rs757471157 | snp | C/T | 1.67489e-05 | 0.00289381 | intron-variant | USP40 | GRCh38.p7 | 2:233540623 | ATCATAATGAAATTT[C/T]TTGGGACTAGGACTT | 55230 |
rs757488047 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233550073 | CTCTTCTGGCTTTGA[C/T]GTCTAAACTCAAGTC | 55230 |
rs757517517 | snp | C/G | 1.65734e-05 | 0.00287862 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523423 | CATCACTGCTTGTGT[C/G]TAGATGAAGAACATT | 55230 |
rs757520105 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233557143 | GATCAGATATAAGAA[G/T]GACTCAGCAAAACAA | 55230 |
rs757528644 | snp | C/T | 1.71619e-05 | 0.00292928 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485594 | CAAATAATCTTGTTT[C/T]TTTTTCTTTTTCCTC | 55230 |
rs757534268 | snp | C/G | 5.52471e-05 | 0.00525552 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233529491 | AAATGACATGGAACC[C/G]CATATCTTGGATTAG | 55230 |
rs757590503 | snp | A/G | 1.68579e-05 | 0.00290321 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233521010 | TTAACAGTTGCTGAT[A/G]TTTTAACTTGCTTCT | 55230 |
rs757596918 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233522202 | ACTTATCTACAAAAT[-/A]ATCATTATTAGGTTT | 55230 |
rs757625855 | snp | A/T | 2.29893e-05 | 0.0033903 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551481 | AAATCTTAGTAATGA[A/T]ACAGTAAGAAAAGGA | 55230 |
rs757649981 | in-del | -/GTTAC | | | intron-variant | USP40 | GRCh38.p7 | 2:233513469 | GAAATGAAGTCAATG[-/GTTAC]TGCTTGTGGTGCACA | 55230 |
rs757651711 | in-del | -/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233496692 | TCCCTAAATGAGGCT[-/G]TATCATCTCTGTAAT | 55230 |
rs757682624 | snp | C/G | 0.00021546 | 0.0103771 | intron-variant | USP40 | GRCh38.p7 | 2:233477543 | TGACTCATGGATGCA[C/G]TGGGTGTCAGGGTGA | 55230 |
rs757700264 | snp | A/G | 2.35037e-05 | 0.00342802 | intron-variant | USP40 | GRCh38.p7 | 2:233527594 | CTTTAAAGAGGCACA[A/G]AAATACATAAATACT | 55230 |
rs757706772 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233499650 | ACATTCCTACTTTGT[A/G]CCTTTGCTGGATCCT | 55230 |
rs757712212 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233522575 | AATATTGCAGTTACA[A/G]TGTATGACACATTGA | 55230 |
rs757757238 | snp | A/C | | | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233488293 | TCAATTCTCCGTCCT[A/C]GTTTATATTCCCTGA | 55230 |
rs757758917 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233523990 | TGATCTAGCATCTGA[C/T]GCACAACCTGGTATA | 55230 |
rs757770385 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233537982 | AATTTACATTACATG[A/T]AATGGTAAAATATAA | 55230 |
rs757770526 | snp | A/T | 3.33912e-05 | 0.00408589 | intron-variant | USP40 | GRCh38.p7 | 2:233488326 | ATAAGTGAAACAAGA[A/T]AATATTGAGTGACAT | 55230 |
rs757792290 | snp | C/T | 5.13106e-05 | 0.00506484 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551404 | GGCTTGAGATTAATC[C/T]GGAGAGGGAATGTAT | 55230 |
rs757802229 | snp | C/T | 5.54893e-05 | 0.00526703 | intron-variant | USP40 | GRCh38.p7 | 2:233499948 | GTCCAATGTTAGTTT[C/T]CTGTTTCTGAGTTAC | 55230 |
rs757815390 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233478186 | ATATCCTGGTAGGCA[C/T]GCGTCCATGTTTTTG | 55230 |
rs757830099 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233500069 | TAAGAAGATAATACA[C/T]GAGTCAGCTTTCCTT | 55230 |
rs757870960 | snp | A/G | 1.6577e-05 | 0.00287893 | intron-variant | USP40 | GRCh38.p7 | 2:233488206 | GGTTAAGATACGTGT[A/G]TGTCACTTCAGATGC | 55230 |
rs757880152 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233483287 | CTGAACTCTCCTGTT[C/T]AAGACCAGCCTGGGC | 55230 |
rs757880320 | snp | A/G | 1.66385e-05 | 0.00288426 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233496763 | AAAATCTTACCAGAG[A/G]AGGAAGTTGTCCTTC | 55230 |
rs757893753 | in-del | -/ACAG | 1.65778e-05 | 0.002879 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556916 | CAATGGTTCCATGGT[-/ACAG]ACAGACGATAGATGA | 55230 |
rs757922639 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233531605 | GAACCATTTCCATAT[C/T]TTTTTTTCCTCCCAG | 55230 |
rs757965838 | snp | A/G | 2.43638e-05 | 0.00349017 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233559868 | GGATGCAGCTTCCTG[A/G]TCTAAGAGCAGAAGC | 55230 |
rs757973561 | snp | C/T | 1.67713e-05 | 0.00289575 | intron-variant | USP40 | GRCh38.p7 | 2:233557057 | ATGTAATTCCGGGCT[C/T]CAGATTTTTTAAAAC | 55230 |
rs758003506 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233530778 | CATTTCCCCAATTTA[A/C]TACTGAGCACAATGA | 55230 |
rs758020229 | snp | C/G | 4.97146e-05 | 0.00498546 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233540740 | AAGTTTCTGGCCCAG[C/G]TGATCAACAGGAATT | 55230 |
rs758027271 | in-del | -/GCAATAAC | 0.000162489 | 0.00901212 | intron-variant | USP40 | GRCh38.p7 | 2:233540816 | CTGATGAGAAATAAT[-/GCAATAAC]TGCATACTTAACAAA | 55230 |
rs758035650 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233507957 | GTACCCCATAAATAC[A/G]TGTCAATTTAATTTT | 55230 |
rs758074365 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233494076 | AGGTTTATTAAGAGA[C/T]AAAAGGTGCTATTGT | 55230 |
rs758102224 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233566526 | GGTTTCGGGCCACGG[G/T]GACCTCTGCCTTTTT | 55230 |
rs758148468 | snp | A/G | 0.000132747 | 0.00814591 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233554485 | AGCATCTTCCAAACC[A/G]GATACATTTTTGACT | 55230 |
rs758154247 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233551050 | AAAATGACTCTAAAT[A/G]AATCAGTGGTTCTCA | 55230 |
rs758161255 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233544906 | TTTGTGTCCCAAATT[C/T]ATACTAGCTGTATTG | 55230 |
rs758194653 | snp | A/T | 2.67212e-05 | 0.00365512 | intron-variant | USP40 | GRCh38.p7 | 2:233511801 | AGCTGTCCGGCACTT[A/T]AAAAAATTTTGATAA | 55230 |
rs758202530 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233516513 | CCATCCTGGCTAACA[C/T]GGTGAAACCCTGTCT | 55230 |
rs758237424 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233483968 | TTTCCTCACGTGTGT[C/G]ATTCTGTTTCTGGGC | 55230 |
rs758262124 | in-del | -/TT | | | intron-variant | USP40 | GRCh38.p7 | 2:233517385 | CATGCATGGTTTTTT[-/TT]GTTTTTTTTTTTTTT | 55230 |
rs758282264 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233501599 | TAATGAACAGAATGA[G/T]ATGTGGTCAGATCCT | 55230 |
rs758298358 | snp | G/T | 2.59024e-05 | 0.00359868 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485891 | GCAGTCCCACCCTGG[G/T]CCGCGTTCCACACCA | 55230 |
rs758337047 | snp | G/T | 3.47078e-05 | 0.00416565 | intron-variant | USP40 | GRCh38.p7 | 2:233527362 | GAGAGTCTAGCTGGA[G/T]ATGGTGCTCGATGTC | 55230 |
rs758343169 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233531715 | ATGCAAATTAGTAAC[G/T]GCTTTATTCTTATTC | 55230 |
rs758378985 | snp | A/G | 1.65649e-05 | 0.00287788 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523399 | CTATCACCTGACAAC[A/G]CTTTTCTCCATCACT | 55230 |
rs758417915 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233518470 | TACTTGGGAGGCTGA[A/G]GCAGAAAAATTGCTT | 55230 |
rs758428556 | in-del | -/C | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233566693 | ACTTACTGCCTAAAG[-/C]CCAGACCCCCGCCCT | 55230 |
rs758459191 | in-del | -/AA | | | intron-variant | USP40 | GRCh38.p7 | 2:233481355 | TTTTAGCCTACATTT[-/AA]AAGAGGCATGTCTAA | 55230 |
rs758469424 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233514564 | TTATTCAGGTTCTTG[C/T]AGGCTAGGTTAAGGA | 55230 |
rs758478050 | in-del | -/AA | | | intron-variant | USP40 | GRCh38.p7 | 2:233555961 | CTACTAAAAAAATAC[-/AA]AAAATTAGCCAGGCA | 55230 |
rs758479109 | snp | A/G | | | stop-gained, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527523 | TGAAGAAATGATACT[A/G]AGGGCCCAGGTGAAG | 55230 |
rs758559475 | snp | A/G | 1.80781e-05 | 0.00300645 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485508 | TCTTCTCAAAGTGGT[A/G]AATTTGCTGTTAAAC | 55230 |
rs758603237 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233513646 | GTAGTAATGAAATTC[A/G]TGCATGTCAGAGCAG | 55230 |
rs758624202 | in-del | -/A | 0.000420477 | 0.0144935 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486017 | CAGATCCAAACAAAC[-/A]AACAAAACCACGTGG | 55230 |
rs758630356 | snp | C/T | 1.76018e-05 | 0.00296658 | intron-variant | USP40 | GRCh38.p7 | 2:233554564 | ATTGAAAAACAATTT[C/T]AGAGGTTTACAAACA | 55230 |
rs758678247 | snp | A/G | 3.46759e-05 | 0.00416374 | stop-gained, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233491169 | GAAGAAGTCTGACCT[A/G]AGACTTCAGCTCCGC | 55230 |
rs758791800 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233522392 | GGAATGTCTGCAAAA[C/T]CCCTGTCCAAAAGAG | 55230 |
rs758805087 | in-del | -/ATG | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562727 | TGCAAAGGTATTTTT[-/ATG]ATTATTATTATTATT | 55230 |
rs758811927 | in-del | -/T | 5.9625e-05 | 0.00545976 | frameshift-variant, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233481261 | CAGTGTCATCTCTGA[-/T]TGTACTGAAATCATC | 55230 |
rs758823390 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233478744 | AGGACACCACGCTCC[C/T]ACCATGAGACGGGGC | 55230 |
rs758824698 | snp | A/G | 3.8227e-05 | 0.00437173 | intron-variant | USP40 | GRCh38.p7 | 2:233488192 | CAAAAGGCAAACGAG[A/G]TTAAGATACGTGTGT | 55230 |
rs758847448 | in-del | -/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233523918 | TACTCCAGCACGTAT[-/G]GTGCAGTTCTTCACA | 55230 |
rs758904520 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233478387 | ATGTGGCACTGTCTC[A/G]GAGTAGCTTGAATTT | 55230 |
rs758909102 | snp | G/T | 1.9911e-05 | 0.00315517 | intron-variant | USP40 | GRCh38.p7 | 2:233499833 | AAAAGTCAAAAAAAT[G/T]TTTATTAGGCTTTTA | 55230 |
rs758932992 | snp | A/G | 6.5848e-05 | 0.00573756 | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233561171 | ATACCTTTGCATCGG[A/G]TTTATCCTTATCTTC | 55230 |
rs758939077 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233534705 | TGCAGCTAGTTTGTT[C/T]AAGGTACAAAAAAGT | 55230 |
rs758954849 | snp | C/T | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486071 | GCTTCTCCTCCAGCT[C/T]TTCTGGTTTTTATAA | 55230 |
rs758956424 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233500331 | TCCCTTCTCTCTTCT[A/C]TTTATGACTGTCTGA | 55230 |
rs758964383 | snp | A/G | 3.78924e-05 | 0.00435256 | splice-donor-variant | USP40 | GRCh38.p7 | 2:233481201 | CAGACCCCAGCAATT[A/G]CCTTTTCCTTCTCCC | 55230 |
rs758969961 | snp | A/G | 1.85486e-05 | 0.00304531 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523484 | TTGAATGTGGACTCC[A/G]CCAACCTGCAATCAT | 55230 |
rs758999791 | snp | A/G | 5.04392e-05 | 0.00502166 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233498580 | CTCCAGCTTCATAGC[A/G]CCAATCCATTTTTCG | 55230 |
rs759023027 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233488896 | TGGGCGACAGAGCCA[C/G]ACCCTGTCTATTAAG | 55230 |
rs759026881 | snp | A/G | 1.65971e-05 | 0.00288067 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533501 | GGGTCTCTGCAACTG[A/G]GATTTCCGATAAAAC | 55230 |
rs759044695 | in-del | -/TTT | | | intron-variant | USP40 | GRCh38.p7 | 2:233547570 | GCTATGCTTTAAGCA[-/TTT]TACATCCTAACATTA | 55230 |
rs759124627 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233536536 | CATGCCAGTAATCTC[A/T]GCTACTCGGGAGGCT | 55230 |
rs759179189 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233488752 | GACCTCGTCAAAACA[A/G]AAAATTAGCCTGGTG | 55230 |
rs759195475 | snp | A/T | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486674 | TAGATGTACTTCTAT[A/T]AAGTGTTTTTACCAT | 55230 |
rs759195624 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233497354 | TTTCTGAGGAGATTT[C/T]CCAGATCAATCTGGC | 55230 |
rs759217258 | snp | C/T | 0.000129291 | 0.0080392 | intron-variant | USP40 | GRCh38.p7 | 2:233489362 | GTCCAGCAAGGAACC[C/T]ACCTGAGTGGCTGCC | 55230 |
rs759230053 | snp | G/T | 2.14007e-05 | 0.00327107 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551465 | TCACAAAATCAAAAT[G/T]AAATCTTAGTAATGA | 55230 |
rs759235878 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233500810 | TCACAGAAGCAAAGC[A/G]CACTCTTCATTTCTA | 55230 |
rs759243262 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233537628 | AGTTGGCTTCTCATC[C/T]AACATACTGGAAGCC | 55230 |
rs759247921 | snp | C/T | 5.02332e-05 | 0.00501139 | intron-variant | USP40 | GRCh38.p7 | 2:233496872 | GTCACTTATGACTTC[C/T]GAAAGGAGCAGATCA | 55230 |
rs759254283 | in-del | -/ACT | | | intron-variant | USP40 | GRCh38.p7 | 2:233488720 | GGAGTTCGCGACCAG[-/ACT]GGGCAACATAGGGAG | 55230 |
rs759305013 | snp | A/G | 6.91874e-05 | 0.00588123 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233488288 | AGATCTCAATTCTCC[A/G]TCCTAGTTTATATTC | 55230 |
rs759309313 | in-del | -/AG | | | intron-variant | USP40 | GRCh38.p7 | 2:233564484 | ATGGGAGAAATATAT[-/AG]AGAGAAACAGGGGCA | 55230 |
rs759413224 | snp | C/T | 3.31208e-05 | 0.00406931 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523327 | CACCTGCTGGGATTG[C/T]TAAGGCTGTGAGGAC | 55230 |
rs759437931 | in-del | -/A | 8.8574e-05 | 0.00665426 | intron-variant | USP40 | GRCh38.p7 | 2:233498637 | AGTCAAAATTGGGAT[-/A]AAAAAAATTCAAAGT | 55230 |
rs759459735 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233510812 | GTTTTTTCTGAGTCA[C/T]TTGGTTATGATTTTA | 55230 |
rs759461050 | snp | G/T | 1.67036e-05 | 0.0028899 | intron-variant | USP40 | GRCh38.p7 | 2:233496740 | TTAAGAGTTGTCTAT[G/T]CAGAAGTAAAATCTT | 55230 |
rs759495911 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233509140 | CTGCTGCTACCAGGT[G/T]GGTCACTCTTTCCAA | 55230 |
rs759505046 | snp | C/G | 1.65811e-05 | 0.00287929 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523220 | GCTTCCATTTCTGAG[C/G]CCTTGCTCCCTGAAC | 55230 |
rs759546330 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233558155 | GGATAGAAAACTTGT[A/G]GAAGTTTTCAAGCTC | 55230 |
rs759558539 | snp | C/T | 2.44807e-05 | 0.00349854 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233559858 | GGTCTGCTGTGGATG[C/T]AGCTTCCTGGTCTAA | 55230 |
rs759565481 | snp | C/G/T | 3.84194e-05 | 0.00438272 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233481296 | TCGTCAATCAGGAGA[C/G/T]TCTACATTTCAAAAG | 55230 |
rs759599377 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233545441 | TGCCAATTGGGTGCT[A/G]TCATGGAGCCTTCTT | 55230 |
rs759612368 | snp | A/G | 1.72127e-05 | 0.00293361 | intron-variant | USP40 | GRCh38.p7 | 2:233554544 | GAAATAGACATGAAT[A/G]TAATATTGAAAAACA | 55230 |
rs759644026 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233481669 | TGTTTACTTTATAGA[A/C]ACCGTCAGTCTGTTC | 55230 |
rs759652946 | snp | A/C | | | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233512575 | AAGATTTACCTGGAC[A/C]AAGAAGCTTCCCATT | 55230 |
rs759693587 | snp | A/C | 1.69364e-05 | 0.00290997 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477407 | TTATCTGAAGCTCCC[A/C]ACGTGGATGGAGAGA | 55230 |
rs759700850 | snp | A/G | 6.69916e-05 | 0.00578717 | intron-variant | USP40 | GRCh38.p7 | 2:233525601 | AGAGAATGTTGAAAA[A/G]TGACATATACATATC | 55230 |
rs759727707 | in-del | -/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233483551 | TATGTCTTCTAAAGA[-/T]TTGAAAATGAGTGGT | 55230 |
rs759738562 | snp | G/T | 1.67806e-05 | 0.00289656 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527445 | CTCCTAAAGTTTTTC[G/T]TTTATCAAAGGTCAA | 55230 |
rs759746204 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233554096 | ACAGAAATAAAAATA[C/T]ATACAACTTTTTTCA | 55230 |
rs759750662 | in-del | -/A | 1.6585e-05 | 0.00287962 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533631 | GAGATGCTATTGTTT[-/A]AACCTGGGGATTCTG | 55230 |
rs759752703 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233520502 | TGAGATGGTGTTTAA[C/T]GAAACTAGTCTTCAA | 55230 |
rs759792467 | snp | A/G | 1.79551e-05 | 0.0029962 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477373 | AGTTCATCGGGAGTA[A/G]AGCCGTGCAGCGGCG | 55230 |
rs759810751 | in-del | -/CTCCCTGAACGTCTTC | 1.6571e-05 | 0.0028784 | frameshift-variant, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523225 | ATTTCTGAGCCCTTG[-/CTCCCTGAACGTCTTC]CTCCCTGAACGTCTT | 55230 |
rs759839395 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233498260 | CCTTCATGAGCTCAA[A/G]TGTCATTTGTTCTGT | 55230 |
rs759873169 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233505951 | GAATTTAACAAGCAC[A/G]TTAAAAAGACCATTC | 55230 |
rs759874639 | snp | A/G | 2.08989e-05 | 0.00323249 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533767 | GAAATATCTGAGAAT[A/G]GAGCTGTAAGAACTA | 55230 |
rs759902878 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233528315 | TAGCATGAACCTCCC[A/G]AGACCACATTATCCA | 55230 |
rs759950096 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233563286 | ATGGCAGTGGTCTTA[C/T]CTGGAAAAAGAAGTT | 55230 |
rs759955461 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233515891 | TTGAGGTTCATTTCT[A/G]CACATACAAATATCT | 55230 |
rs759971353 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233549335 | ATAAGAAACTTCACT[C/G]TTTGTTATTTAAGAG | 55230 |
rs759973889 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233538727 | ATTAGCAGAGATAAA[C/G]ACAAGCATTTCTGGT | 55230 |
rs759987475 | snp | A/G | 5.68209e-05 | 0.00532984 | intron-variant | USP40 | GRCh38.p7 | 2:233493365 | GACTCTCAGAGCACA[A/G]GCAGTCAATTTACTT | 55230 |
rs759989342 | snp | C/T | 0.00026888 | 0.0115917 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485567 | GTCTTTCAAGTAATA[C/T]GGTGCCCCTTGCAAA | 55230 |
rs760072451 | snp | C/T | 3.59441e-05 | 0.00423919 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527555 | TGCAATTCAAAAGTA[C/T]TGTTTGCAGAATCAC | 55230 |
rs760098063 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233482279 | TGAGGCAGAAGAGTC[A/G]CTTGAACTCGGGAGG | 55230 |
rs760103167 | snp | G/T | 3.29832e-05 | 0.00406085 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233488274 | AAGGGGCTCTAAGCA[G/T]ATCTCAATTCTCCGT | 55230 |
rs760155060 | snp | C/T | 7.60529e-05 | 0.00616609 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551444 | TTTCCTTGTAGCGTT[C/T]GCATTTCACAAAATC | 55230 |
rs760186524 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233514484 | CGCAGAAAAGTCAGC[A/T]TGGGAAGTGAGTTGT | 55230 |
rs760197186 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233514388 | TAAACAGCTGAAGTT[A/G]AAAGCAAAGGGAAGA | 55230 |
rs760212328 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233477848 | ACACACACCGCTGCA[C/T]GACTCGTCACAATCA | 55230 |
rs760297539 | in-del | -/CTCT | | | intron-variant | USP40 | GRCh38.p7 | 2:233492617 | GCTCATTCAACATTA[-/CTCT]CTCTATATAATCCTA | 55230 |
rs760317092 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233541753 | ACTTTAAAAGTCATC[A/T]ACTTGAGATATTATC | 55230 |
rs760318458 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233564011 | GTGTTATCCCTATTA[A/G]AAATGTACTTATTAG | 55230 |
rs760338441 | snp | A/T | 2.63828e-05 | 0.0036319 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233559836 | GTCCACCCAAAGCTG[A/T]CAGTGAGGTCTGCTG | 55230 |
rs760346226 | snp | A/G | 5.43178e-05 | 0.00521114 | intron-variant | USP40 | GRCh38.p7 | 2:233499920 | AACTTTAAACACTGT[A/G]AAGAAAAACAATGTC | 55230 |
rs760373531 | snp | C/T | | | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233549136 | AATGATCAACATCTT[C/T]AATATATACATGGTA | 55230 |
rs760409175 | snp | A/G | 1.85792e-05 | 0.00304783 | intron-variant | USP40 | GRCh38.p7 | 2:233498658 | AATTCAAAGTTAGGT[A/G]AGACGTTGCGTGTAA | 55230 |
rs760481459 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233527766 | TCAGTTCTGTCACCA[A/T]GAATTCCAAGAGAAA | 55230 |
rs760497237 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233509039 | TTCCTGACCTAGATA[C/T]ATAACCAGCCATTAT | 55230 |
rs760534596 | in-del | -/AT | | | intron-variant | USP40 | GRCh38.p7 | 2:233492389 | GTTGTTAAGTGACAC[-/AT]GAGTGCATTTCCCAT | 55230 |
rs760536043 | snp | C/T | 3.45286e-05 | 0.00415489 | stop-gained, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233493495 | GTCCTGATGACTCTC[C/T]CAGTGTCCTGAGGGA | 55230 |
rs760596187 | snp | C/G/T | 6.68979e-05 | 0.00578317 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523447 | GAACATTTAAAAGTA[C/G/T]AGGTTCGCAGTCAAT | 55230 |
rs760657667 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233478373 | TGTTGCCAATAGGCA[G/T]GTGGCACTGTCTCGG | 55230 |
rs760667398 | in-del | -/GT | | | intron-variant | USP40 | GRCh38.p7 | 2:233491608 | ACCTGTTCCTCGTGT[-/GT]GTGTGTGTGTGTGTG | 55230 |
rs760684799 | snp | C/T | 1.70901e-05 | 0.00292314 | splice-donor-variant | USP40 | GRCh38.p7 | 2:233529430 | AGCAATTTAAAATTA[C/T]CTTTTGGTTTGCAGT | 55230 |
rs760693781 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233553804 | TTTTCCCTCTTAGCT[A/C]TCACATGGCAAAAGA | 55230 |
rs760786805 | in-del | -/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233532292 | ATAAGTGTAACGTTG[-/T]TAACTTCAACCTAGC | 55230 |
rs760801139 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477001 | CATCTGAACACGGAG[G/T]AAAGTGGCTGGCCTG | 55230 |
rs760860911 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233540189 | CAAGCAACACTGATG[A/G]AAAAAGGTGAGAAAA | 55230 |
rs760959752 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233505848 | GATTCCAAGACCAGA[A/T]GTAGATTCAACAACA | 55230 |
rs760988857 | snp | C/T | 1.72196e-05 | 0.00293419 | intron-variant | USP40 | GRCh38.p7 | 2:233559968 | TGAATTCTTTAAGTG[C/T]TGACTAAGGCTTTTG | 55230 |
rs761001537 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233551830 | CTTTCACCTTCATCC[C/T]TGGTGTCTCCACTTT | 55230 |
rs761021322 | snp | A/C | 3.34818e-05 | 0.00409143 | intron-variant | USP40 | GRCh38.p7 | 2:233496730 | CAATTATTACTTAAG[A/C]GTTGTCTATTCAGAA | 55230 |
rs761024253 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233519102 | TTAGTGGTTGCCAGG[A/G]GCTTGGAATACAGAT | 55230 |
rs761026769 | snp | A/G | 0.00145397 | 0.0269234 | intron-variant | USP40 | GRCh38.p7 | 2:233490994 | AGGCCACGAGGAGCC[A/G]TCTGCACCATGGGCG | 55230 |
rs761029533 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476353 | CTGCTGTCTGGGAAA[A/G]TCAACCGTCTATGTC | 55230 |
rs761042199 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233563084 | ATCAGAAATCTTTCA[C/T]GGCTTCCCACTGTCT | 55230 |
rs761057220 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233490932 | GCAAGTCACTGAGGA[C/T]AGATTGAAACAAAAG | 55230 |
rs761109081 | in-del | -/A | 1.65685e-05 | 0.00287819 | frameshift-variant, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551490 | TAATGAAACAGTAAG[-/A]AAAGGAGGCAGCTTA | 55230 |
rs761115436 | snp | C/T | 2.82211e-05 | 0.00375629 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233512555 | ACCTTTTGAAAGTTA[C/T]CAAAAAGATTTACCT | 55230 |
rs761140400 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233505754 | ACATTTAAAGAATAT[C/T]AATTCTCCTCAAACT | 55230 |
rs761172147 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233516468 | TTTGGAAGGCCTAGG[C/T]GGGCGGATCACGAGG | 55230 |
rs761172607 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233482994 | GCCCACTTCTCTATT[A/G]GGTTATTTTTTGATA | 55230 |
rs761183988 | snp | A/C | 3.99832e-05 | 0.00447102 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233549195 | ATAATAACTGAGAAG[A/C]GGTCATATATATATT | 55230 |
rs761199494 | snp | C/T | 1.95865e-05 | 0.00312936 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233511748 | AAGACACAGTCCCAA[C/T]GAACTTCCCATCTTC | 55230 |
rs761218815 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233542202 | ACATTCTTACATATA[A/T]ACACACATGCACACA | 55230 |
rs761225468 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233484122 | AAGATCGTACCACTG[C/T]ACTCCAGCCTGGGCA | 55230 |
rs761280561 | snp | A/C | 1.65982e-05 | 0.00288077 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233554423 | GTTCCACAGTGGTAC[A/C]AGTTGTCACAATCAA | 55230 |
rs761315180 | in-del | -/AG | 1.85266e-05 | 0.00304351 | intron-variant | USP40 | GRCh38.p7 | 2:233477516 | TGGCTGCAGAGACAC[-/AG]ACACTGTCATTGACT | 55230 |
rs761322605 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476738 | TGCAGCGGCTGCCCT[C/T]GCTTAGCAGAGCGAC | 55230 |
rs761323425 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233527326 | TGAAAAATAAAGTTG[C/T]ATCCTAAACAGAATG | 55230 |
rs761416421 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233547713 | AAATTCTTTTTTTGA[A/G]AAATATTATAAAACT | 55230 |
rs761419219 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233546885 | ACAACACGATAAGGA[C/T]TGGCTCAAATTAAAC | 55230 |
rs761428956 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233546121 | AGAGCTTCAAAAATG[C/G]ACAGGCAGTGCAGAG | 55230 |
rs761436582 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233532708 | GCATTTTGGGAGGCT[A/G]AGGTGTGAGCATCAT | 55230 |
rs761441801 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233512984 | AAACCCTCTTCGTTA[C/T]TAATATTATACATGT | 55230 |
rs761479838 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233517058 | TTTCTTAATTTTGAT[A/G]TCGATTTTGTTGTTG | 55230 |
rs761488921 | snp | A/G | 0.000172058 | 0.00927358 | intron-variant | USP40 | GRCh38.p7 | 2:233529395 | ATCTTTATTCTCCGG[A/G]ATACTAGTCAAACTC | 55230 |
rs761502004 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233560864 | TTTAAATAGACTTCT[C/G]GGGGAAGCTAATGTG | 55230 |
rs761579899 | snp | A/G | 6.72914e-05 | 0.0058001 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485552 | ACCAATAGTATCTCC[A/G]TCTTTCAAGTAATAC | 55230 |
rs761660691 | in-del | -/ATA | 0.0331383 | 0.124383 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562710 | CCTAAAACTTAAAGT[-/ATA]ATAATAATAATAATA | 55230 |
rs761673293 | snp | A/C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233522022 | CTGAGCAGAGAAAGA[A/C/T]GAAATACCTTGCCCA | 55230 |
rs761675077 | snp | A/C | 1.72829e-05 | 0.00293959 | intron-variant | USP40 | GRCh38.p7 | 2:233520963 | AACTGAAAATCTATC[A/C]GCCAACCTTTAATTA | 55230 |
rs761693987 | snp | C/T | 0.000286622 | 0.0119678 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477431 | GGAGAGAGAAGTTTC[C/T]GGGGCTCGGGGCCGG | 55230 |
rs761706272 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233499866 | TAATATGTCATCATG[C/G]TAAGTAACTTACCTT | 55230 |
rs761731598 | snp | G/T | 1.75173e-05 | 0.00295945 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527545 | CAGGTGAAGATGCAA[G/T]TCAAAAGTATTGTTT | 55230 |
rs761735788 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233484454 | ATCTAATCATTTATC[C/T]GTGTAGTCTTTTGAA | 55230 |
rs761748632 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233530609 | GAAATGTCACCTGTT[A/G]AAACCCAAGAGTCAC | 55230 |
rs761748833 | in-del | -/TTAG | | | intron-variant | USP40 | GRCh38.p7 | 2:233492545 | AAGGCATTTTTAGCA[-/TTAG]TTAACATGAACTACT | 55230 |
rs761775648 | snp | C/T | 0.00011821 | 0.00768708 | intron-variant, synonymous-codon | USP40 | GRCh38.p7 | 2:233488007 | GGGGTCAATATGCAC[C/T]TGGTGATTACTGAAA | 55230 |
rs761785282 | in-del | -/T | 1.78979e-05 | 0.00299143 | frameshift-variant, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233499908 | TTCTTCAGCATTAAC[-/T]TTAAACACTGTAAAG | 55230 |
rs761796318 | snp | A/G | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486455 | GGAAGAGAGACACAG[A/G]GCGGGTGAGACACAA | 55230 |
rs761797035 | in-del | -/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233496481 | ATTAGTAAAACATTA[-/C]CCTTGGATATGATGA | 55230 |
rs761799994 | in-del | -/AGACT | | | intron-variant | USP40 | GRCh38.p7 | 2:233497965 | GACCACAGCTCCCTC[-/AGACT]CCCCACAGAGCTTTA | 55230 |
rs761825692 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476338 | CTGCTTTCCGCTAAG[C/G]TGCTGTCTGGGAAAG | 55230 |
rs761851606 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233517961 | ATGTTCTCACTGATA[C/T]GTGGGAGCTAAGCTA | 55230 |
rs761861913 | snp | C/T | 4.975e-05 | 0.00498724 | intron-variant, splice-acceptor-variant | USP40 | GRCh38.p7 | 2:233540770 | TAGATTATTCTCCTC[C/T]TTATGAGAGAAACAC | 55230 |
rs761917506 | snp | A/C/T | 8.33779e-05 | 0.00645626 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233524509 | CCACCCCATTCCACA[A/C/T]AAAGATGTCTTCCCC | 55230 |
rs761920623 | in-del | -/AG | | | intron-variant | USP40 | GRCh38.p7 | 2:233537372 | CTCCCAGAAAAAGAA[-/AG]AGAGATGAGGCAGAA | 55230 |
rs761945954 | snp | G/T | 1.83125e-05 | 0.00302587 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485810 | TTTTCGGGAAAGTAT[G/T]TGGCAATTTCAATCT | 55230 |
rs761956910 | snp | A/G | 1.65688e-05 | 0.00287821 | stop-gained, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556986 | CGCTGAAGAGGATTC[A/G]ATTCAGTTCCTGCAC | 55230 |
rs761982184 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233508817 | CCATTATAGGTAACT[A/G]CACATTTTTGTATAG | 55230 |
rs762004506 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233550629 | CAATAGCTAGCTAAT[A/G]AATGTTCTATTCTGA | 55230 |
rs762023763 | snp | A/G | 3.43036e-05 | 0.00414133 | splice-donor-variant | USP40 | GRCh38.p7 | 2:233559809 | AGAGCTGATCCTCGT[A/G]CCTCATTACTGGTCC | 55230 |
rs762029590 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233545281 | AGGGAAGAGGCAAAC[C/T]GGCAATGTAGAGATG | 55230 |
rs762070958 | snp | C/T | 5.50343e-05 | 0.00524539 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233489377 | TACCTGAGTGGCTGC[C/T]GGTCAGTTCGTAAAA | 55230 |
rs762094176 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233495838 | CTTTAAAGATCATTG[C/T]ACAAAATATAATAGA | 55230 |
rs762135438 | snp | G/T | | | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233566203 | AGACTGCCACTAAAA[G/T]TATCAAGCCTAAAGG | 55230 |
rs762140926 | snp | A/T | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486139 | AACTCTTATTCCGCA[A/T]TTCAATTTCCTTTAA | 55230 |
rs762150089 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233483737 | TAGGGAGGCTCGACC[A/G]TTAAGTATAATGCAA | 55230 |
rs762156868 | snp | C/T | 1.65655e-05 | 0.00287793 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233510105 | CTGTCCCAGGTTGAA[C/T]GTCACTCCCCATTGC | 55230 |
rs762157616 | snp | A/G | 0.000208023 | 0.0101965 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233521084 | AATCTCATTCATACT[A/G]GTGACCCATTTCTCT | 55230 |
rs762178637 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233490857 | AAGGGATAAAGTGAA[C/T]GCTTTACAAATGTTC | 55230 |
rs762213017 | snp | A/G | 1.66579e-05 | 0.00288595 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233554401 | TGCTTTAACCAGCCT[A/G]TCACAAGTTCCACAG | 55230 |
rs762223651 | snp | A/G | 2.21056e-05 | 0.0033245 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233511716 | TATTTTACCTGAGAC[A/G]AACTTGGTGCTTTTC | 55230 |
rs762272748 | snp | G/T | | | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233525506 | GTAAATGTGAAGTCC[G/T]GCTGGTACAAGCTTT | 55230 |
rs762300656 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233541340 | ATTTTAGAGTAGGCC[C/T]TAAGTAAATCTGATT | 55230 |
rs762328090 | snp | C/T | 3.33884e-05 | 0.00408572 | intron-variant | USP40 | GRCh38.p7 | 2:233525433 | TGAGCCGGACAAAAA[C/T]GTAGATATATAGAGT | 55230 |
rs762357022 | in-del | -/CTT | 3.5407e-05 | 0.0042074 | cds-indel, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477496 | TCTGCTCATGGAGGG[-/CTT]CTTGGCTGCAGAGAC | 55230 |
rs762360176 | in-del | -/TC | 8.55864e-05 | 0.00654109 | intron-variant | USP40 | GRCh38.p7 | 2:233554369 | GGGAAAAAGCAGTTA[-/TC]TGTCTTTACCTTTGC | 55230 |
rs762421064 | snp | C/T | 0.000131397 | 0.00810441 | intron-variant | USP40 | GRCh38.p7 | 2:233565333 | GTACATATTGCTAGT[C/T]AAATGTACGTAACAT | 55230 |
rs762433150 | snp | C/T | 1.658e-05 | 0.00287919 | stop-gained, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533603 | ATCATTTATATCAAA[C/T]CAGTGGGGACAGGAG | 55230 |
rs762444740 | in-del | -/GAGC | | | intron-variant | USP40 | GRCh38.p7 | 2:233517669 | TGGGATTACAGGCGT[-/GAGC]CACTGTGCCCGGCCT | 55230 |
rs762448199 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233503767 | TTACAAGAAAATACT[C/T]AAGGGAGCACTACAA | 55230 |
rs762462132 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233539867 | ATATCTAAGGCAAAA[G/T]CTGGTTTCTTGAAAA | 55230 |
rs762495714 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233521222 | GGTGACCAAGTTCTA[C/T]TGAGTCGTCTCTATG | 55230 |
rs762514104 | snp | A/T | 1.65652e-05 | 0.0028779 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523233 | AGCCCTTGCTCCCTG[A/T]ACGTCTTCCTCATGT | 55230 |
rs762532496 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233523779 | TTCACAGAGTGGCTG[A/T]AGTGCTCCTGGCCGC | 55230 |
rs762544486 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233559503 | AATCTCCATGTAATC[A/G]GTGTTGTATCTCAAC | 55230 |
rs762549455 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233558506 | AGTGAAAGAAGACTG[C/T]TACGAGACCACCTAT | 55230 |
rs762571891 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233545680 | CCAGAGAAAATTACA[C/T]GAGATTGGTCCTGAA | 55230 |
rs762595908 | snp | A/G | 0.000439883 | 0.0148239 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485780 | ACCCAGCTAGATATC[A/G]GAAGCCACTCGAACT | 55230 |
rs762624146 | snp | C/T | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486527 | AGAAAGAACAACACT[C/T]AGCAAGGCAGGAGGA | 55230 |
rs762656296 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233525395 | AGGTGGGGAAGGACT[A/G]ACAAAGAGTAGAAAA | 55230 |
rs762678269 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233553315 | GTGAAAAGGAAATAT[-/A]AATGAATGGCTGCTA | 55230 |
rs762702991 | snp | C/T | 3.37439e-05 | 0.00410741 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233554522 | GTTAGATCTAAGAAG[C/T]CTTCCTGAAATAGAC | 55230 |
rs762703756 | snp | C/T | 0.000145264 | 0.00852121 | intron-variant | USP40 | GRCh38.p7 | 2:233489512 | CAGACATTTCTCCAA[C/T]GGTTTTAAAAAGCAC | 55230 |
rs762782339 | snp | A/G | | | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475460 | TGAGCCACCGCGCCC[A/G]GCCAAAAGTTCCTCT | 55230 |
rs762819668 | snp | A/T | 1.71399e-05 | 0.0029274 | intron-variant, missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233498616 | GCCAGGCATCTCCTA[A/T]AAAGGAGTCAAAATT | 55230 |
rs762824172 | snp | A/G | 3.6535e-05 | 0.00427389 | intron-variant | USP40 | GRCh38.p7 | 2:233551345 | TCTTGAGAGGGGAAA[A/G]GAAAGAATTTAAAAA | 55230 |
rs762824317 | snp | C/T | 1.67494e-05 | 0.00289386 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527463 | TATCAAAGGTCAAAT[C/T]CCACACGCTTTCTGT | 55230 |
rs762869338 | in-del | -/GTGT | | | intron-variant | USP40 | GRCh38.p7 | 2:233517782 | GATAAAGAAACTGTG[-/GTGT]GTGTGTGTGTGTGTG | 55230 |
rs762885129 | in-del | -/GAGCTGCCTTCCCCTGCTTTGCACTG/GAGCTGCCTTCCCCTGCTTTGCACTGGCA/GAGCTGCCTTCCCCTGCTTTGCACTGGCAGCACG | 0.000424693 | 0.0145671 | intron-variant | USP40 | GRCh38.p7 | 2:233477539 | CATTGACTCATGGAT[lengthTooLong]GCAGTGGGTGTCAGG | 55230 |
rs762888394 | snp | C/G/T | 7.98284e-05 | 0.00631736 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485949 | CACCAGGGATGCGCA[C/G/T]CTGTGTCCTCAGCAG | 55230 |
rs762895546 | snp | C/T | 6.84556e-05 | 0.00585005 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233549160 | CATGGTAATGGCCTC[C/T]GTAGCAGCCACCTTT | 55230 |
rs762907307 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233529743 | GAAGAATTCCATTTT[C/T]TCAACTCTTTTAAGT | 55230 |
rs762919070 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233497387 | CAATATGCATGACAT[C/T]GAAGCAGGGAACGCC | 55230 |
rs762984992 | snp | A/G | 3.53938e-05 | 0.00420662 | intron-variant | USP40 | GRCh38.p7 | 2:233549085 | AAGATATTTCTAAAC[A/G]AATTTCTATACGTAC | 55230 |
rs762994056 | snp | A/G | 1.65671e-05 | 0.00287807 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556980 | CCAAAGCGCTGAAGA[A/G]GATTCGATTCAGTTC | 55230 |
rs763006910 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233484881 | TTGGCAGTGAGGGAG[A/G]GAATTCATTGCCCGT | 55230 |
rs763028517 | snp | C/T | 2.22057e-05 | 0.00333202 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233491250 | CTTGCGCAGGCTCGT[C/T]CCCAGAAGCACCTTC | 55230 |
rs763076026 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233479797 | CACAGGTCCTTTGCT[A/G]TCCTGGGGCTCCCGG | 55230 |
rs763111148 | in-del | -/T | 4.54081e-05 | 0.00476466 | frameshift-variant, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233510069 | CACAGATATTGTTTC[-/T]TTCTACTACGATTTC | 55230 |
rs763118179 | snp | C/T | 1.65921e-05 | 0.00288024 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233512613 | ATAGGTCTCAAACAG[C/T]TGTTGTCAGCTATAT | 55230 |
rs763241638 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233507332 | ACTGGGTATGTGTCC[A/G]AAGGGTATGAAATCA | 55230 |
rs763264664 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233536018 | ACTAAAATTTATCAA[C/T]TTGTAATTAAAAAAT | 55230 |
rs763286399 | snp | A/G | 1.71894e-05 | 0.00293162 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527535 | ACTGAGGGCCCAGGT[A/G]AAGATGCAATTCAAA | 55230 |
rs763306683 | snp | C/T | 0.000133864 | 0.00818011 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233524494 | TAATTTTTTTTACCT[C/T]CACCCCATTCCACAC | 55230 |
rs763315819 | in-del | -/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233490330 | ACCGTGCCAGGTGAA[-/T]TTTTTTTTTTTTTGT | 55230 |
rs763324501 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233502028 | AGTCATCAGGTACAT[C/T]GAATGTTGGTGATAG | 55230 |
rs763326892 | snp | A/C | 6.57981e-05 | 0.00573539 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562833 | AGAATCAGAGATGCA[A/C]ATGACATCATTTCAT | 55230 |
rs763360200 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233549476 | CAAGTACCTGAAAAA[C/T]ACGTTACTTTTATGT | 55230 |
rs763365780 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233524599 | GACCATTCATCATGA[C/T]CATCAGAAACAACTG | 55230 |
rs763398592 | snp | G/T | 1.65729e-05 | 0.00287857 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233540672 | ATTACCTTCCGCAGT[G/T]GTCCATGCTGTTTTC | 55230 |
rs763399414 | snp | C/G/T | 5.48826e-05 | 0.0052382 | intron-variant | USP40 | GRCh38.p7 | 2:233499935 | AAAGAAAAACAATGT[C/G/T]CAATGTTAGTTTTCT | 55230 |
rs763405308 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233516687 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 55230 |
rs763409088 | snp | C/T | 1.67925e-05 | 0.00289758 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233493469 | CCCCAAGACGAAGTA[C/T]AGTTGGTCTGGTCCT | 55230 |
rs763451863 | snp | A/T | 1.7117e-05 | 0.00292544 | intron-variant | USP40 | GRCh38.p7 | 2:233561114 | CTTCTTTAAAAAAAA[A/T]TTTCTGAATACGCTA | 55230 |
rs763452173 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233559542 | ATAAAGACTCTTAGG[A/G]TAGAAATTGTAAAAA | 55230 |
rs763463846 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233538027 | GAAAAATGGGAATGG[A/G]AAAATGAAATTATAC | 55230 |
rs763466277 | snp | G/T | | | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233568536 | AATCTTATATCTTTA[G/T]AAATGTGACCACTCA | 55230 |
rs763489426 | snp | C/T | 1.93601e-05 | 0.00311122 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485739 | GCCGGTAAGCCCCAA[C/T]TTCTCTGAGACAGCC | 55230 |
rs763519072 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233509387 | ACCACTGTGTGTGTA[C/T]ATAAATACTAGAAAA | 55230 |
rs763521339 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233542021 | ACTTATACTTTTTAT[C/T]TTTTGTATATATTTT | 55230 |
rs763544624 | snp | A/T | 1.77344e-05 | 0.00297773 | intron-variant | USP40 | GRCh38.p7 | 2:233498517 | CATAAATGTAATCAT[A/T]CGAAAGTACAATGTA | 55230 |
rs763547138 | snp | C/T | | | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233566136 | CCGAAGCTGTTGGGC[C/T]GGAAGTCAGTTCACT | 55230 |
rs763578075 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233546635 | GGAAGAAAAGAGCCA[C/T]GAACTGCAATGGGAA | 55230 |
rs763598399 | snp | C/T | 3.42612e-05 | 0.00413877 | intron-variant | USP40 | GRCh38.p7 | 2:233549089 | TATTTCTAAACGAAT[C/T]TCTATACGTACTTGA | 55230 |
rs763636511 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233545726 | GCAGTACCTACTAAA[C/G]AACTCCATGTATGCA | 55230 |
rs763638738 | snp | C/T | 3.31312e-05 | 0.00406995 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523235 | CCCTTGCTCCCTGAA[C/T]GTCTTCCTCATGTCT | 55230 |
rs763682660 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233509478 | TTTTAATCAATTTCT[A/G]CACATTCAACATTTC | 55230 |
rs763688551 | snp | A/G | 1.72943e-05 | 0.00294055 | intron-variant | USP40 | GRCh38.p7 | 2:233559974 | CTTTAAGTGTTGACT[A/G]AGGCTTTTGAAAACA | 55230 |
rs763696607 | snp | A/G | 1.65608e-05 | 0.00287752 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523339 | TTGCTAAGGCTGTGA[A/G]GACAGTGCCCACTTC | 55230 |
rs763705927 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233510853 | AGGGTTTCAAATATT[A/G]CAATTCTCAAGACTC | 55230 |
rs763720954 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233547965 | GTCCTACCAGAGATC[-/A]AGACTTATTACAAAG | 55230 |
rs763757555 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233525690 | GAATACTCTCACCCC[C/T]ACCCAACACCGAAAA | 55230 |
rs763769002 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233496193 | TGGGGCCATTTGTTT[C/T]TCTTTTGGGTTCACT | 55230 |
rs763770982 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233510898 | AAATCTGATCTCTTA[C/T]TCAGTTCCTCATAGC | 55230 |
rs763807244 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233552431 | ATAGAATAGAATATA[A/G]ATTTAGAAGTATCAA | 55230 |
rs763821442 | in-del | -/AAAGGAAAG | | | intron-variant | USP40 | GRCh38.p7 | 2:233488922 | TTAAGAAAAGAAAGA[-/AAAGGAAAG]AAAGGAAAGAAAGAA | 55230 |
rs763849474 | snp | C/T | 1.87429e-05 | 0.00306123 | intron-variant | USP40 | GRCh38.p7 | 2:233485482 | CTCTATAAAATCATG[C/T]GACCCTCGTGTCTTC | 55230 |
rs763854294 | snp | A/G | 8.81484e-05 | 0.00663826 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477378 | ATCGGGAGTAGAGCC[A/G]TGCAGCGGCGCGGTT | 55230 |
rs763872258 | in-del | -/A | | | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233565781 | GACCCTGGATATGTT[-/A]AATCTGTTTTCTTAT | 55230 |
rs763898415 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233513687 | CTGCCTATATTTAAA[A/C]TATGTTGGGTGATTT | 55230 |
rs763906235 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233519171 | AAACTGGATTGTGGT[A/G]ATGGTTATAGAACTC | 55230 |
rs763920678 | snp | C/G | | | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477423 | ACGTGGATGGAGAGA[C/G]AAGTTTCCGGGGCTC | 55230 |
rs763921071 | snp | C/T | 3.66818e-05 | 0.00428247 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233512626 | AGCTGTTGTCAGCTA[C/T]ATATAAAAGGAATAT | 55230 |
rs763929760 | snp | A/G | 0.000137637 | 0.00829454 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233549161 | ATGGTAATGGCCTCC[A/G]TAGCAGCCACCTTTG | 55230 |
rs763932253 | snp | C/G | 0.00011873 | 0.00770394 | intron-variant, missense | USP40 | GRCh38.p7 | 2:233487989 | ACACTTCAGGGCCAT[C/G]ATGGGGTCAATATGC | 55230 |
rs763935935 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233484905 | TGCCCGTGTTGTTTA[A/G]TACAGTGTTAAACAG | 55230 |
rs764010577 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233504687 | ATATATGCAAACACC[A/G]CCAGAACACCCAAAT | 55230 |
rs764025570 | snp | A/G | 7.47566e-05 | 0.00611332 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523487 | AATGTGGACTCCACC[A/G]ACCTGCAATCATACC | 55230 |
rs764036137 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233514621 | TAAAGGGCTTTGTGC[A/G]GAGGAGTGACAGGAT | 55230 |
rs764038258 | snp | A/G | 1.92158e-05 | 0.0030996 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485747 | GCCCCAATTTCTCTG[A/G]GACAGCCCCACAACT | 55230 |
rs764089848 | snp | A/G | 1.65715e-05 | 0.00287845 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233540677 | CTTCCGCAGTGGTCC[A/G]TGCTGTTTTCTGTAC | 55230 |
rs764096838 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233532511 | AGATTCTGTATCTGG[A/G]CCCTTGAGCTGCTGC | 55230 |
rs764113317 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233529747 | AATTCCATTTTTTCA[A/G]CTCTTTTAAGTATAC | 55230 |
rs764113518 | snp | A/T | | | synonymous-codon, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485821 | GTATTTGGCAATTTC[A/T]ATCTTCTCCACGGGA | 55230 |
rs764117468 | snp | C/T | 0.000156054 | 0.0088319 | intron-variant | USP40 | GRCh38.p7 | 2:233527371 | GCTGGAGATGGTGCT[C/T]GATGTCTGAATTAAG | 55230 |
rs764142594 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233500340 | TCTTCTCTTTATGAC[A/T]GTCTGAATTTCCCCG | 55230 |
rs764152852 | snp | A/G | | | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233493436 | TCACCTTGGCTGGAA[A/G]TGGCTCTCCAAACTC | 55230 |
rs764160485 | in-del | -/AC | | | intron-variant | USP40 | GRCh38.p7 | 2:233492415 | TCCCATGTGTTGTGT[-/AC]AGATGTATTACCAAA | 55230 |
rs764245001 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233482853 | GTGTGGGAGTTCCCA[C/T]GGTCTCACTAGCAAG | 55230 |
rs764250503 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233502430 | TAAGTAACCTCAATC[C/T]AAAAATCTAAATATG | 55230 |
rs764265928 | snp | A/G | 3.3145e-05 | 0.0040708 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556923 | TTCCATGGTACAGAC[A/G]ATAGATGAGGTCATG | 55230 |
rs764272023 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233544425 | TTAAATAAATCACTC[A/G]TCACTGGTGACTGAA | 55230 |
rs764283341 | snp | C/T | 1.71897e-05 | 0.00293164 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485592 | TGCAAATAATCTTGT[C/T]TTTTTTTCTTTTTCC | 55230 |
rs764304426 | snp | C/T | 2.25233e-05 | 0.00335576 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551478 | ATTAAATCTTAGTAA[C/T]GAAACAGTAAGAAAA | 55230 |
rs764314481 | snp | C/T | 3.70913e-05 | 0.00430631 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233510085 | TTCTACTACGATTTC[C/T]ATTTCTGTCCCAGGT | 55230 |
rs764323776 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233549478 | AGTACCTGAAAAATA[C/T]GTTACTTTTATGTAC | 55230 |
rs764367856 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233523857 | CCCCAACTCAGTATA[C/G]ATTCTCACTCTTCTA | 55230 |
rs764371265 | snp | A/G | 2.26652e-05 | 0.00336632 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233491256 | CAGGCTCGTTCCCAG[A/G]AGCACCTTCCAAAGG | 55230 |
rs764398070 | snp | A/G | 0.000197239 | 0.00992877 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562836 | ATCAGAGATGCAAAT[A/G]ACATCATTTCATTTT | 55230 |
rs764405213 | snp | A/G | 0.000550863 | 0.016587 | intron-variant | USP40 | GRCh38.p7 | 2:233519715 | AGTTGTAAAAAATGG[A/G]AGGAGATGAAAATGA | 55230 |
rs764407369 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233563401 | TTCCTACCTAGGCTC[A/G]GATACAGACTTCTCA | 55230 |
rs764424159 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233546660 | GGGAATGGGCAAGGC[-/A]AAAAAAAATGAACAC | 55230 |
rs764478376 | in-del | -/AAAG | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477273 | GCCGTCCCTGTGCTC[-/AAAG]GAAGCAGAGGATTTG | 55230 |
rs764524189 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233483024 | AACAGATTTGCAGAA[G/T]ATCTGCTGTCTATGC | 55230 |
rs764548952 | snp | A/G | 1.70755e-05 | 0.00292189 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551397 | ACAAAAGGGCTTGAG[A/G]TTAATCCGGAGAGGG | 55230 |
rs764576905 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233484299 | TGGGAAGAACTGATA[A/C]CTTTACTATTGTGAG | 55230 |
rs764600237 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233501229 | GGGAAATAGAGAGCA[G/T]AAAAGCCTTATTTCA | 55230 |
rs764601534 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233478757 | CCCACCATGAGACGG[A/G]GCAGCTGAGTACACA | 55230 |
rs764621887 | in-del | -/G | 3.46179e-05 | 0.00416026 | intron-variant | USP40 | GRCh38.p7 | 2:233554354 | CAAAGTGGGGACCCT[-/G]GGAAAAAGCAGTTAT | 55230 |
rs764639174 | snp | C/T | 1.84684e-05 | 0.00303873 | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233561254 | AAAAAGAGCCCGCAT[C/T]GCCAAGTCAATCCTA | 55230 |
rs764661619 | snp | C/G | 1.67016e-05 | 0.00288973 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233524500 | TTTTTACCTCCACCC[C/G]ATTCCACACAAAGAT | 55230 |
rs764677334 | in-del | -/AAA | 0.000309981 | 0.0124457 | intron-variant | USP40 | GRCh38.p7 | 2:233533792 | GAACTACACAGAAAC[-/AAA]AAAAAAAATGCTAAG | 55230 |
rs764712761 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233509298 | CTGTTTTCCAATACT[A/C]AAGGTCTCAGTTCTC | 55230 |
rs764754718 | snp | A/G | 1.78315e-05 | 0.00298587 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233493508 | TCCCAGTGTCCTGAG[A/G]GACCCTGAAGCTGGT | 55230 |
rs764764905 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233514438 | GCACTAAGAAGTCTT[A/G]GGGGTTAAAGAGAGC | 55230 |
rs764770303 | snp | C/T | 1.65875e-05 | 0.00287984 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533508 | TGCAACTGGGATTTC[C/T]GATAAAACAACATGT | 55230 |
rs764774772 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233507781 | TCTATTGTACAGTAG[A/G]GTGATGATAGTTAAC | 55230 |
rs764777547 | snp | A/G | | | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556868 | ACCTGCCTCTCGCTA[A/G]CGTTCTTACATTCTT | 55230 |
rs764781716 | in-del | -/AA | 1.65697e-05 | 0.0028783 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233540723 | ATTCCTATCTTTTTC[-/AA]AAGTTTCTGGCCCAG | 55230 |
rs764846535 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233537656 | GCCAGAACACAATGG[A/G]CCTCTTTAAAACACT | 55230 |
rs764863953 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233484516 | GACAGGATCTCTGTT[A/G]CCTGGGCTGCAGTGC | 55230 |
rs764879748 | in-del | -/TATAGCTATATGATCTTATATAAGAG | | | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233567231 | GATCTTATATAAGAT[-/TATAGCTATATGATCTTATATAAGAG]TATAGCTATATGATC | 55230 |
rs764897906 | snp | C/T | 1.65649e-05 | 0.00287788 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233481205 | CCCCAGCAATTACCT[C/T]TTCCTTCTCCCCAGG | 55230 |
rs764901952 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233544805 | CTTACAATAAAGGAC[A/C]ATGAGGAACTGGCTT | 55230 |
rs764956344 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233478595 | GCAGAAATCTGTCCT[A/T]CAGATATATCCACAT | 55230 |
rs764966752 | in-del | -/TGAGCTGCCTTCCCC/TGAGCTGCCTTCCCCTGCTT | 0.000403542 | 0.0141994 | intron-variant | USP40 | GRCh38.p7 | 2:233477538 | TCATTGACTCATGGA[lengthTooLong]TGCAGTGGGTGTCAG | 55230 |
rs764969261 | in-del | -/TGT | | | intron-variant | USP40 | GRCh38.p7 | 2:233491631 | GTGTGTGTGTGTGTG[-/TGT]GTCTGTCTGTCTGTG | 55230 |
rs764984074 | snp | A/G | 6.19023e-05 | 0.00556303 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233489368 | CAAGGAACCTACCTG[A/G]GTGGCTGCCGGTCAG | 55230 |
rs765013281 | snp | A/C | | | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233566565 | GACTCCAGGAGAGCG[A/C]CGCGTCCTCAGGCAG | 55230 |
rs765026211 | snp | A/G | 1.67837e-05 | 0.00289682 | intron-variant | USP40 | GRCh38.p7 | 2:233525604 | GAATGTTGAAAAGTG[A/G]CATATACATATCACC | 55230 |
rs765056429 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233530648 | TATCTGATTTGGTGG[A/G]GCATCTCACTAATGT | 55230 |
rs765085393 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233518370 | TCAGGAGTTTGAGAC[C/T]AGCCTGGCCAACATG | 55230 |
rs765093065 | snp | A/G | 1.66916e-05 | 0.00288886 | intron-variant | USP40 | GRCh38.p7 | 2:233496743 | AGAGTTGTCTATTCA[A/G]AAGTAAAATCTTACC | 55230 |
rs765145167 | snp | C/G | 0.000149248 | 0.00863723 | intron-variant | USP40 | GRCh38.p7 | 2:233549072 | AAAAGAAATTGCAAA[C/G]ATATTTCTAAACGAA | 55230 |
rs765181308 | snp | C/T | | | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527415 | ATATTACCTGAAATA[C/T]TGACTGCCGGAGATC | 55230 |
rs765204976 | snp | A/C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233564289 | GACAGCCTGACTCAT[A/C/G]CTATCTGGTTTGCCA | 55230 |
rs765211068 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233542360 | CTGGTTTACTTTTTT[C/T]CTCCTAGGAAGGAAA | 55230 |
rs765235133 | snp | A/T | 3.43177e-05 | 0.00414218 | intron-variant | USP40 | GRCh38.p7 | 2:233559964 | TAAATGAATTCTTTA[A/T]GTGTTGACTAAGGCT | 55230 |
rs765237555 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233545449 | GGGTGCTGTCATGGA[A/G]CCTTCTTTGCCCCAC | 55230 |
rs765268591 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233506963 | TTATATAAGGAACTT[A/G]AACAATTCAACAGCA | 55230 |
rs765292480 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233483941 | TTAATGTTGCCTCAA[G/T]TATCTGTCACATTTC | 55230 |
rs765294082 | in-del | -/TTTCTG | 3.68704e-05 | 0.00429347 | intron-variant | USP40 | GRCh38.p7 | 2:233499946 | ATGTCCAATGTTAGT[-/TTTCTG]TTTCTGAGTTACAGT | 55230 |
rs765308294 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543130 | CATGTCAAAATTCCC[C/T]GGTAAGTTATTTTCA | 55230 |
rs765321196 | snp | C/T | 2.43852e-05 | 0.0034917 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233559861 | CTGCTGTGGATGCAG[C/T]TTCCTGGTCTAAGAG | 55230 |
rs765323603 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233478327 | CCCCAGTGACTCTGC[A/G]TCCTCAACACACGAG | 55230 |
rs765354237 | snp | A/G | 3.35773e-05 | 0.00409726 | intron-variant | USP40 | GRCh38.p7 | 2:233491121 | TTAATATCTCACTGG[A/G]AGAAGCCACATTACC | 55230 |
rs765354842 | in-del | -/CGCGTT | 2.61236e-05 | 0.00361402 | cds-indel, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485892 | AGTCCCACCCTGGGC[-/CGCGTT]CGCGTTCCACACCAG | 55230 |
rs765363341 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233528394 | TCCACTTGGCTGACT[C/T]GAAGCCAGTGCGAAA | 55230 |
rs765380776 | snp | C/T | | | intron-variant, splice-acceptor-variant | USP40 | GRCh38.p7 | 2:233491072 | CCATATCAGAACAGA[C/T]TGTAATTGAGGGAAA | 55230 |
rs765403697 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233492001 | AGTTCCTCTTGTGTC[C/T]TAAGGAAATTACAGG | 55230 |
rs765570818 | snp | A/G | 1.78522e-05 | 0.0029876 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477375 | TTCATCGGGAGTAGA[A/G]CCGTGCAGCGGCGCG | 55230 |
rs765611454 | snp | A/G | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486296 | TGGCAGAGAGGGACA[A/G]GGTGAGAGAGGCCTG | 55230 |
rs765640065 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233532506 | GGAGAAGATTCTGTA[G/T]CTGGGCCCTTGAGCT | 55230 |
rs765651884 | snp | C/T | 7.56401e-05 | 0.00614934 | intron-variant | USP40 | GRCh38.p7 | 2:233498662 | CAAAGTTAGGTGAGA[C/T]GTTGCGTGTAACTTC | 55230 |
rs765655293 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233536576 | GGACTGCTTGAGCCT[G/T]GGAGGCAGAGATTGC | 55230 |
rs765657329 | snp | C/G | 1.65545e-05 | 0.00287697 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485732 | TTGCTATGCCGGTAA[C/G]CCCCAATTTCTCTGA | 55230 |
rs765693647 | in-del | -/AT | 1.65822e-05 | 0.00287938 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233554459 | TCCTCTTCTACATAC[-/AT]GTTCCAGAGAGCATC | 55230 |
rs765696711 | in-del | -/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233522573 | GAAATATTGCAGTTA[-/C]AGTGTATGACACATT | 55230 |
rs765726962 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233482835 | CACTGCGCCTGGCCA[C/T]GTGTGTGGGAGTTCC | 55230 |
rs765737578 | snp | C/T | 5.50433e-05 | 0.00524582 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523480 | CAGTTTGAATGTGGA[C/T]TCCACCAACCTGCAA | 55230 |
rs765747545 | snp | A/G/T | 3.36209e-05 | 0.00409995 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485568 | TCTTTCAAGTAATAC[A/G/T]GTGCCCCTTGCAAAT | 55230 |
rs765747947 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233500907 | GATGTGGATAAGATG[A/T]TGTTATCTGATTGCA | 55230 |
rs765768770 | snp | A/G | 4.22181e-05 | 0.00459427 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533768 | AAATATCTGAGAATG[A/G]AGCTGTAAGAACTAC | 55230 |
rs765792157 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233502739 | CCGTAACCTAGGAAA[C/T]TGAGGCAACTGCACA | 55230 |
rs765807676 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233548339 | CTATTGTGAAAGCTA[C/T]AGACACGGGATTTAT | 55230 |
rs765812133 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233522165 | AAGGTTGGGCAGGGG[G/T]AATGGAAAGCAGGAT | 55230 |
rs765823651 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233514504 | AAGTGAGTTGTGAGT[A/T]CGCAGAAAAGCAGAT | 55230 |
rs765827623 | snp | A/G | 0.000115937 | 0.00761283 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523389 | TGTGGAGATTCTATC[A/G]CCTGACAACACTTTT | 55230 |
rs765832196 | in-del | -/GTGTGC/GTGTGTGG | | | intron-variant | USP40 | GRCh38.p7 | 2:233479646 | TGTGTGTGTGTGTGT[-/GTGTGC/GTGTGTGG]GTGTGTGTGTGTGTC | 55230 |
rs765837006 | in-del | -/AC | | | intron-variant | USP40 | GRCh38.p7 | 2:233480265 | CCAGATCAGGCTCCT[-/AC]AGTCATTTGGGCAGG | 55230 |
rs765854861 | snp | C/T | 1.72196e-05 | 0.00293419 | intron-variant | USP40 | GRCh38.p7 | 2:233520969 | AAATCTATCAGCCAA[C/T]CTTTAATTATATTCT | 55230 |
rs765883438 | snp | C/T | 1.7149e-05 | 0.00292817 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477487 | TGTAGCTGCTCTGCT[C/T]ATGGAGGGCTTCTTG | 55230 |
rs765896913 | snp | A/G | 1.91613e-05 | 0.0030952 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551445 | TTCCTTGTAGCGTTC[A/G]CATTTCACAAAATCA | 55230 |
rs765905164 | snp | C/T | 1.8276e-05 | 0.00302286 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527560 | TTCAAAAGTATTGTT[C/T]GCAGAATCACATTCT | 55230 |
rs765954825 | snp | A/G/T | 0.000115139 | 0.00758658 | intron-variant | USP40 | GRCh38.p7 | 2:233488189 | CTTCAAAAGGCAAAC[A/G/T]AGGTTAAGATACGTG | 55230 |
rs765990199 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233500044 | TTGAATAGGCAAGGA[G/T]AGACATAGTTAAGAA | 55230 |
rs765996333 | in-del | -/TG | | | intron-variant | USP40 | GRCh38.p7 | 2:233478032 | TTTGGCCCAGCCTGA[-/TG]TGTGTGGCCCACCCA | 55230 |
rs766039543 | in-del | -/T | 1.65666e-05 | 0.00287802 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556974 | AAGTTTCCAAAGCGC[-/T]GAAGAGGATTCGATT | 55230 |
rs766051115 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233506551 | GCAAAAGAAACAACA[C/G]AGTAAAGAGACAACC | 55230 |
rs766138737 | snp | A/G | 1.81017e-05 | 0.00300841 | intron-variant | USP40 | GRCh38.p7 | 2:233499922 | CTTTAAACACTGTAA[A/G]GAAAAACAATGTCCA | 55230 |
rs766139988 | snp | G/T | 1.66654e-05 | 0.00288659 | intron-variant | USP40 | GRCh38.p7 | 2:233540817 | CTGATGAGAAATAAT[G/T]GCATACTTAACAAAT | 55230 |
rs766162256 | snp | A/C/T | 3.34657e-05 | 0.00409047 | intron-variant | USP40 | GRCh38.p7 | 2:233496732 | ATTATTACTTAAGAG[A/C/T]TGTCTATTCAGAAGT | 55230 |
rs766162881 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233546391 | AACCTGAAGATGAAA[C/T]TGCAAACAGATATTT | 55230 |
rs766225013 | snp | A/C | 7.33353e-05 | 0.00605494 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233521110 | TCTCTTCCTTGGTCA[A/C]CAAGCTGTAGGTAAA | 55230 |
rs766232693 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233530522 | ATTACTGGTTTAAAC[A/G]GTATGACAGTTTCAA | 55230 |
rs766240160 | snp | C/T | 1.86201e-05 | 0.00305118 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485825 | TTGGCAATTTCAATC[C/T]TCTCCACGGGAAGAC | 55230 |
rs766251472 | snp | C/G | 4.11159e-05 | 0.0045339 | intron-variant | USP40 | GRCh38.p7 | 2:233481192 | ACATCTGTGCAGACC[C/G]CAGCAATTACCTTTT | 55230 |
rs766259829 | snp | A/C/T | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543398 | AAAACTCTTCTGAGG[A/C/T]CAAAAAAGTGAAATG | 55230 |
rs766294252 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233478380 | AATAGGCATGTGGCA[C/G]TGTCTCGGAGTAGCT | 55230 |
rs766303299 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233475571 | TTTAACAAAATCGTA[C/T]AGCTTTCTCAATCCC | 55230 |
rs766317311 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233554098 | AGAAATAAAAATATA[C/T]ACAACTTTTTTCACA | 55230 |
rs766323989 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233495892 | ATAAGGTAGGTGTGT[A/T]TGTGCTGATATGAGG | 55230 |
rs766340074 | in-del | -/T | 0.000106536 | 0.00729771 | frameshift-variant, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485591 | TTGCAAATAATCTTG[-/T]TTTTTTTTCTTTTTC | 55230 |
rs766357588 | in-del | -/TGTG | | | intron-variant | USP40 | GRCh38.p7 | 2:233517676 | ACAGGCGTGAGCCAC[-/TGTG]CCCGGCCTGCACATG | 55230 |
rs766398496 | snp | A/G | 2.02616e-05 | 0.00318283 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233511765 | AACTTCCCATCTTCA[A/G]TTCTGCTTCCTTCAA | 55230 |
rs766410925 | snp | A/C | 1.66949e-05 | 0.00288915 | intron-variant | USP40 | GRCh38.p7 | 2:233525591 | ATGAAGGAAAAGAGA[A/C]TGTTGAAAAGTGACA | 55230 |
rs766484610 | snp | C/T | 0.000341344 | 0.0130597 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233510117 | GAACGTCACTCCCCA[C/T]TGCAAAAAACAGGAA | 55230 |
rs766488184 | in-del | -/CTTCA | | | intron-variant | USP40 | GRCh38.p7 | 2:233491887 | CTAAATTTAGACTGT[-/CTTCA]CTTATTTTTGCCTTA | 55230 |
rs766495091 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233491008 | CGTCTGCACCATGGG[C/T]GTGTATTGCCTGCGG | 55230 |
rs766495666 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233519103 | TAGTGGTTGCCAGGG[G/T]CTTGGAATACAGATG | 55230 |
rs766505634 | snp | A/G | 0.00011607 | 0.00761718 | intron-variant | USP40 | GRCh38.p7 | 2:233542410 | CTAACCCCTTAAAAA[A/G]TAACAAAATAGGAAT | 55230 |
rs766531676 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233502524 | TTTGGATTTTGCAAT[C/G]TGGCAGTGGCCCTGC | 55230 |
rs766544361 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233551914 | TGGGACCTAGGAACC[C/T]GTTTTAAAGGATCTG | 55230 |
rs766595405 | snp | C/T | 3.31219e-05 | 0.00406938 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523354 | GGACAGTGCCCACTT[C/T]TGCATTAGCTGGAAA | 55230 |
rs766610339 | snp | A/G | 1.66568e-05 | 0.00288585 | intron-variant | USP40 | GRCh38.p7 | 2:233525451 | AGATATATAGAGTGA[A/G]TTGCTATGTTTTCAT | 55230 |
rs766617483 | in-del | -/C | 6.89727e-05 | 0.0058721 | frameshift-variant, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233510120 | CGTCACTCCCCATTG[-/C]AAAAAACAGGAACAA | 55230 |
rs766621632 | snp | C/G | | | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233489401 | CGTAAAAGCCTGCCT[C/G]GGCGCTTCCTCTCCA | 55230 |
rs766624301 | snp | C/T | 1.68134e-05 | 0.00289938 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485554 | CAATAGTATCTCCGT[C/T]TTTCAAGTAATACGG | 55230 |
rs766635326 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233525700 | ACCCCCACCCAACAC[C/T]GAAAACTTGAAAAGA | 55230 |
rs766667002 | in-del | -/TTAA | | | intron-variant | USP40 | GRCh38.p7 | 2:233538103 | TTGTAATTTATCATG[-/TTAA]TTTATATATAGTGTA | 55230 |
rs766696819 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476388 | ATCAATCAACTCAGT[G/T]ACACAGGTACTATTA | 55230 |
rs766720606 | in-del | -/CT | | | intron-variant | USP40 | GRCh38.p7 | 2:233507894 | AGTATGCTAAATACC[-/CT]CTGATTTAATCATTA | 55230 |
rs766722715 | in-del | -/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233536296 | TAAGTGGAAAGACTA[-/C]AACTAAAAAGTATAA | 55230 |
rs766779883 | in-del | -/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233507310 | ATGTGATTCACCAAT[-/C]CCCATTACTGGGTAT | 55230 |
rs766790486 | in-del | -/TTACT | | | intron-variant | USP40 | GRCh38.p7 | 2:233530478 | CATATACAGCTCTGA[-/TTACT]TTAAGACAAACTTGT | 55230 |
rs766791293 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233548122 | ATTGGTAGAGAAAAA[A/T]TGATTACTCAATAAA | 55230 |
rs766879852 | snp | C/T | 1.6582e-05 | 0.00287936 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533625 | GGACAGGAGATGCTA[C/T]TGTTTAAACCTGGGG | 55230 |
rs766969418 | snp | C/T | 1.65787e-05 | 0.00287907 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533529 | AACAACATGTAGGCA[C/T]TTTCTTTACCCTGAA | 55230 |
rs766982376 | snp | A/G/T | 3.34886e-05 | 0.00409187 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527483 | ACGCTTTCTGTTTGA[A/G/T]AGACTACTGGGTGCA | 55230 |
rs766985507 | in-del | -/GCA | | | intron-variant | USP40 | GRCh38.p7 | 2:233489853 | ACAAGGGACACAACA[-/GCA]GCCTTCTTCCGTGCC | 55230 |
rs767005470 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233534363 | AAAAATTTCTTTCTC[C/T]ATTGCCTGTCTCTAC | 55230 |
rs767053699 | snp | G/T | 1.65954e-05 | 0.00288053 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233554426 | CCACAGTGGTACAAG[G/T]TGTCACAATCAAAAA | 55230 |
rs767088839 | snp | A/C | 4.09777e-05 | 0.00452628 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233549199 | TAACTGAGAAGAGGT[A/C]ATATATATATTCTAA | 55230 |
rs767094071 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233497626 | TCCAAGGGTAATGAG[C/T]TGGCTTCTGGCTGAA | 55230 |
rs767137053 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233519393 | GTATCTGGGGAAGGA[A/G]AGAAAGAATAGGTCT | 55230 |
rs767139279 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233536422 | TCCAAATTGAAGTAG[A/G]AAAAGAAAAAAATTA | 55230 |
rs767187802 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233485145 | TCTCTTGAGTCTGGC[A/G]GGATTATTTCTTACA | 55230 |
rs767224127 | snp | A/G | 4.97055e-05 | 0.00498501 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556930 | GTACAGACGATAGAT[A/G]AGGTCATGACCGGAG | 55230 |
rs767226627 | snp | G/T | 0.000109391 | 0.00739484 | intron-variant | USP40 | GRCh38.p7 | 2:233560981 | ACTTGGAAAACTGAT[G/T]CTTTCTCGGAAGGCA | 55230 |
rs767284954 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233555399 | TTTTAAGAGATTTTG[A/G]GGAATGAAAATAGGG | 55230 |
rs767368334 | snp | A/G | 1.68021e-05 | 0.0028984 | intron-variant | USP40 | GRCh38.p7 | 2:233493398 | CTTTATGATGCACTG[A/G]CTGCTGAAATCCCAT | 55230 |
rs767369985 | snp | G/T | 1.7079e-05 | 0.00292219 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477483 | AGGATGTAGCTGCTC[G/T]GCTCATGGAGGGCTT | 55230 |
rs767434721 | snp | C/T | 1.8553e-05 | 0.00304568 | intron-variant | USP40 | GRCh38.p7 | 2:233499949 | TCCAATGTTAGTTTT[C/T]TGTTTCTGAGTTACA | 55230 |
rs767461272 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233501470 | AGGATCACTCAACTT[C/T]TTATAAGAACAGACC | 55230 |
rs767504876 | snp | A/T | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233487239 | GTTTGCAAAAATGCC[A/T]GAACTTATTAGTCAT | 55230 |
rs767510011 | in-del | -/CAC | 1.99507e-05 | 0.00315832 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485677 | TCAACCTCAAGTTCT[-/CAC]TAACTTCTCTATCAC | 55230 |
rs767524911 | snp | C/T | 1.66941e-05 | 0.00288908 | intron-variant | USP40 | GRCh38.p7 | 2:233525435 | AGCCGGACAAAAATG[C/T]AGATATATAGAGTGA | 55230 |
rs767544185 | snp | A/G | 5.59409e-05 | 0.00528842 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233512653 | ATATTATTTTTCTTA[A/G]AGAGCTAGGAATTAA | 55230 |
rs767547207 | snp | A/G | 1.83825e-05 | 0.00303165 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485813 | TCGGGAAAGTATTTG[A/G]CAATTTCAATCTTCT | 55230 |
rs767609000 | snp | C/G | 1.65886e-05 | 0.00287993 | intron-variant | USP40 | GRCh38.p7 | 2:233540777 | TTCTCCTCCTTATGA[C/G]AGAAACACAGTCACT | 55230 |
rs767646491 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233530968 | TTACCTTAAGATCAA[A/C]TATTTATATTTTACA | 55230 |
rs767651081 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233475656 | ACAGGCCGGCCCGGC[C/T]GCACGCGCCTGCTGG | 55230 |
rs767698957 | snp | C/G | 3.31389e-05 | 0.00407042 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233540698 | TTTTCTGTACTTCTT[C/G]TTCCAAGATATTCCT | 55230 |
rs767727117 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233525632 | ACCTTTCCAGGTTAC[C/T]GTGCCAACTCACATA | 55230 |
rs767730792 | snp | C/T | 0.000383068 | 0.0138343 | intron-variant | USP40 | GRCh38.p7 | 2:233489525 | AACGGTTTTAAAAAG[C/T]ACTCTTCAAAACATA | 55230 |
rs767766680 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233538001 | GGTAAAATATAAGAA[G/T]GCAATAGTAGGAAAA | 55230 |
rs767781759 | snp | A/C | 1.89701e-05 | 0.00307972 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485754 | TTTCTCTGAGACAGC[A/C]CCACAACTTTACCCA | 55230 |
rs767801111 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233558742 | GAACTGTACCACTTA[A/G]AAGAGTGAATTCTGT | 55230 |
rs767808797 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233480368 | CCGTGAGTCGGGGAG[C/T]GGGGGAGGATGAGGA | 55230 |
rs767818451 | snp | A/G | | | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233566428 | AGACAACGAGCTCGA[A/G]GCTAGACTCTCGAGT | 55230 |
rs767833794 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233511029 | GGGGGAAGTGGTTGG[C/G]AAAGTAATGAAGTGA | 55230 |
rs767839630 | snp | C/T | 1.65751e-05 | 0.00287876 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556997 | ATTCGATTCAGTTCC[C/T]GCACATCATGTTGCC | 55230 |
rs767853288 | snp | G/T | 5.08634e-05 | 0.00504273 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233493481 | GTACAGTTGGTCTGG[G/T]CCTGATGACTCTCCC | 55230 |
rs767860022 | in-del | -/C | 1.65619e-05 | 0.00287762 | frameshift-variant, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523276 | TGGCCGTCCAACCCT[-/C]CCCACCTGGACATCC | 55230 |
rs767892902 | in-del | -/GT | | | intron-variant | USP40 | GRCh38.p7 | 2:233479630 | TATAGAATTTTACGT[-/GT]GTGTGTGTGTGTGTG | 55230 |
rs767926453 | snp | C/T | 0.000155756 | 0.00882348 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233559920 | TGTAAAGGGATGATT[C/T]GAACCTGAATGAGAA | 55230 |
rs767951261 | snp | A/G | 2.94217e-05 | 0.00383536 | stop-gained, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233481228 | TCCCCAGGGCCCGTT[A/G]TTTCTGCTTTTCTTT | 55230 |
rs767959484 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233510512 | AGTTCAAGCGATTCT[C/T]CTACCTCAGCCTCCC | 55230 |
rs768000702 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233489240 | ACCCAAGTCACAAGC[A/G]TGGCATGACCAGGAA | 55230 |
rs768001361 | snp | A/T | 1.70333e-05 | 0.00291828 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523456 | AAAGTAGAGGTTCGC[A/T]GTCAATACCAGTTTG | 55230 |
rs768013847 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233526780 | GGCAAGACATTGAGT[C/T]TCTTTAAATCACACT | 55230 |
rs768028943 | snp | A/G | 3.3216e-05 | 0.00407515 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233554415 | TGTCACAAGTTCCAC[A/G]GTGGTACAAGTTGTC | 55230 |
rs768041567 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233524215 | GCTCACAGCAACCTC[A/C]ACTTTCCGGGTTCAA | 55230 |
rs768102752 | snp | C/G | 2.33702e-05 | 0.00341827 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551485 | CTTAGTAATGAAACA[C/G]TAAGAAAAGGAGGCA | 55230 |
rs768110608 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233539923 | CAGATCACTTGAGTC[C/T]AGGAGTTTGAGACCA | 55230 |
rs768121758 | snp | A/G | 3.10718e-05 | 0.00394144 | intron-variant | USP40 | GRCh38.p7 | 2:233491302 | TACAAGGAACTTGAA[A/G]CTTATTTTGTGTTTC | 55230 |
rs768157511 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233479419 | AATACAAAAATTAGC[C/T]GGGCATAGTGGTGCA | 55230 |
rs768171693 | snp | A/G | | | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233512334 | AACTAGATCAAACCC[A/G]TGAGTAAAATGAGAA | 55230 |
rs768194454 | snp | A/G | 0.000125731 | 0.00792777 | intron-variant | USP40 | GRCh38.p7 | 2:233565342 | GCTAGTTAAATGTAC[A/G]TAACATAGCATACCT | 55230 |
rs768222693 | in-del | -/CT | 5.30818e-05 | 0.00515151 | frameshift-variant, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477494 | CTCTGCTCATGGAGG[-/CT]GCTTCTTGGCTGCAG | 55230 |
rs768229976 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233527896 | AATGCTAGAGACCTG[C/T]TTACATCATTATGTT | 55230 |
rs768237487 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233481139 | TCTCAGTTTCCAAGC[A/G]GGAATAAGAGAGAGT | 55230 |
rs768263893 | snp | A/T | | | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485647 | GGAAAATCAAACATC[A/T]TAAATAAGCAAAACT | 55230 |
rs768271264 | snp | C/T | 1.79509e-05 | 0.00299585 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551434 | TAACAGCTAGTTTCC[C/T]TGTAGCGTTCGCATT | 55230 |
rs768343810 | snp | C/T | 1.68883e-05 | 0.00290584 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485542 | TTACCTTAACACCAA[C/T]AGTATCTCCGTCTTT | 55230 |
rs768371558 | snp | C/T | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486314 | TGAGAGAGGCCTGGC[C/T]TGATAGCCCGGCAGC | 55230 |
rs768406586 | snp | C/T | 3.31428e-05 | 0.00407066 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233488248 | TCTTACCCCAAGTTT[C/T]CGCCTTTCTGAAGGG | 55230 |
rs768413867 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476674 | ATCCAAGGACCTTCT[G/T]ATCACAGAGCACCCA | 55230 |
rs768421610 | snp | A/G | 1.69009e-05 | 0.00290692 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556867 | TACCTGCCTCTCGCT[A/G]ACGTTCTTACATTCT | 55230 |
rs768424991 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233481888 | TCCGTAAATGCTGTC[C/T]ACAGGGAGGACGCCT | 55230 |
rs768455282 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233563792 | TACAAGCAGTGCACA[C/T]TGTGCACTAAGATGT | 55230 |
rs768498250 | in-del | -/AATT | 8.86328e-05 | 0.00665647 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233512663 | TCTTAGAGAGCTAGG[-/AATT]AATAACCTTCATCCT | 55230 |
rs768503394 | snp | A/T | 1.73108e-05 | 0.00294195 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527540 | GGGCCCAGGTGAAGA[A/T]GCAATTCAAAAGTAT | 55230 |
rs768522254 | snp | G/T | 3.63465e-05 | 0.00426285 | intron-variant | USP40 | GRCh38.p7 | 2:233551350 | AGAGGGGAAAAGAAA[G/T]AATTTAAAAATAAAA | 55230 |
rs768548010 | in-del | -/GATATTACCT | 3.41486e-05 | 0.00413197 | intron-variant | USP40 | GRCh38.p7 | 2:233527399 | AAGAGGAAGTAAGGC[-/GATATTACCT]GAAATATTGACTGCC | 55230 |
rs768580914 | snp | A/T | 5.2268e-05 | 0.00511188 | intron-variant | USP40 | GRCh38.p7 | 2:233498629 | TATAAAGGAGTCAAA[A/T]TTGGGATAAAAAAAA | 55230 |
rs768601117 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233499712 | AGTTTTCTTTCAGCA[G/T]GCCAACAAGAACCAG | 55230 |
rs768610120 | snp | C/T | 0.000139402 | 0.00834755 | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233561220 | TGGGCCAAGAGAAAA[C/T]AAAGTTCATATGGAA | 55230 |
rs768740366 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233534651 | ACCCAAAGACAACAT[C/T]GTTAACATTGTGTAT | 55230 |
rs768778604 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233530357 | TCCATTCTATAAGGA[A/G]CATAATTAACCTAAC | 55230 |
rs768779949 | snp | C/G | 1.6955e-05 | 0.00291157 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477469 | TCTCTGCACTGGAGA[C/G]GATGTAGCTGCTCTG | 55230 |
rs768815451 | snp | C/T | 1.76689e-05 | 0.00297223 | intron-variant | USP40 | GRCh38.p7 | 2:233523156 | AAATCCTTTTTCTCT[C/T]GTTAGCGAGTTACCT | 55230 |
rs768846502 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233479231 | TTTGACAGAGAGGAT[A/G]CTTGGAGAAGTCTGA | 55230 |
rs768851397 | snp | C/T | 5.01945e-05 | 0.00500946 | intron-variant | USP40 | GRCh38.p7 | 2:233481165 | AGAGTCAGAGAGGGC[C/T]CTGTCAGCTGCACAT | 55230 |
rs768874065 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233548403 | GATACAAAATTAATA[C/T]TGTGTGTTATCTAAA | 55230 |
rs768892076 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233557717 | TGCTGCTGAGAGCTC[A/C]TTCTGCTGAGAACAG | 55230 |
rs768903110 | snp | A/T | 1.69925e-05 | 0.00291478 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233521058 | CATAAATTTTTAACG[A/T]GGAGCCAGTCAATCT | 55230 |
rs768925393 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233519694 | AGAGAAATAAAATAA[A/T]GACTAAGTTGTAAAA | 55230 |
rs768936534 | snp | A/C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233537431 | ATTTTTCCAAAATTT[A/C/T]AAAAAAGACTTTGGA | 55230 |
rs768937677 | snp | A/G | 1.70606e-05 | 0.00292062 | intron-variant | USP40 | GRCh38.p7 | 2:233524606 | CATCATGACCATCAG[A/G]AACAACTGAGCTAAA | 55230 |
rs768944935 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233495639 | CACACTTCAGTGTGT[C/G]CAAGTGTGTGTGTAT | 55230 |
rs768966144 | snp | C/T | 2.14549e-05 | 0.0032752 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485853 | GACGATAGAAATCGG[C/T]AACTCTCTGCCTCAG | 55230 |
rs769012837 | snp | A/C | 1.6582e-05 | 0.00287936 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233525549 | ACCATGTCTCCTTCC[A/C]AAAATTCTAACAGCT | 55230 |
rs769021636 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233510452 | TTGTTGCCCAGGCTG[A/G]AGTGCAGTGGAGCGA | 55230 |
rs769027477 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233484309 | TGATACCTTTACTAT[G/T]GTGAGGTTTGCCTTC | 55230 |
rs769044659 | in-del | -/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233552224 | AAAAAAAAGTTGAAT[-/G]AAAAAAAAAAAACAA | 55230 |
rs769052135 | snp | C/T | 2.3261e-05 | 0.00341027 | intron-variant | USP40 | GRCh38.p7 | 2:233493571 | AGAATGGAGCATGTT[C/T]AACTGCTGTGATTAC | 55230 |
rs769061272 | snp | A/T | 0.000868295 | 0.0208181 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233542344 | TCTTTCAGATTCACA[A/T]CTGGTTTACTTTTTT | 55230 |
rs769067592 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233539383 | ACAAGTCCTAAGAAA[G/T]TCAAAAGAACTGAAC | 55230 |
rs769091371 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233551628 | ACAGTTCTAAGAGAA[A/G]TATTACATAAACTCA | 55230 |
rs769141781 | snp | A/G | 3.3157e-05 | 0.00407154 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533597 | TTTAGAATCATTTAT[A/G]TCAAACCAGTGGGGA | 55230 |
rs769147975 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233479360 | ACAAGGTCAAGAGAT[C/T]GAGACCATCCTGGCC | 55230 |
rs769149260 | snp | A/G | 6.47207e-05 | 0.00568825 | stop-gained, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233559921 | GTAAAGGGATGATTC[A/G]AACCTGAATGAGAAA | 55230 |
rs769151223 | snp | G/T | 3.31549e-05 | 0.0040714 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233540762 | ACAGGAATTAGATTA[G/T]TCTCCTCCTTATGAG | 55230 |
rs769151357 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476310 | CAGGACATGCGACAC[C/T]GTCTTCGGGATGCTG | 55230 |
rs769167266 | in-del | -/CCT | 1.87503e-05 | 0.00306183 | intron-variant | USP40 | GRCh38.p7 | 2:233485486 | ATAAAATCATGTGAC[-/CCT]CGTGTCTTCTCAAAG | 55230 |
rs769218876 | snp | A/G | 3.64924e-05 | 0.0042714 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485803 | CTCGAACTTTTCGGG[A/G]AAGTATTTGGCAATT | 55230 |
rs769233647 | snp | C/T | 8.38567e-05 | 0.00647467 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233554513 | ACTGCTACTGTTAGA[C/T]CTAAGAAGTCTTCCT | 55230 |
rs769247924 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233518944 | CAATGCAAAGGAACA[A/T]GCTATTGATACGTAC | 55230 |
rs769254726 | snp | A/G | | | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233568640 | CAATCCTTTCATTCC[A/G]TAGCTTCCTCTCCTC | 55230 |
rs769303358 | in-del | -/TAATCT | 6.75562e-05 | 0.0058115 | cds-indel, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485583 | GGTGCCCCTTGCAAA[-/TAATCT]TGTTTTTTTTTCTTT | 55230 |
rs769304285 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233525076 | GTAAATGCTTTCAAA[C/T]TCTCAAAGTATTTCT | 55230 |
rs769311160 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233477583 | GAAGACCCCAAAATA[C/T]ACTCCAATTTTATAG | 55230 |
rs769408920 | in-del | -/G | 4.85802e-05 | 0.00492826 | intron-variant | USP40 | GRCh38.p7 | 2:233493579 | GCATGTTTAACTGCT[-/G]TGATTACAAAGATTA | 55230 |
rs769412018 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233505019 | TATTTTTTCTAACCA[C/T]GATAAAACTAGAAAT | 55230 |
rs769412877 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476271 | GCTGACGAGAAACCG[C/T]GAGGCCCAGGTGACA | 55230 |
rs769471811 | snp | C/T | 1.95173e-05 | 0.00312383 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477364 | CAGCCGGAGAGTTCA[C/T]CGGGAGTAGAGCCGT | 55230 |
rs769480814 | snp | C/T | 1.69109e-05 | 0.00290778 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233554380 | GTTATCTGTCTTTAC[C/T]TTTGCTGCTTTAACC | 55230 |
rs769485922 | snp | C/T | 3.46147e-05 | 0.00416006 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233489472 | CTCCAGGAAAGGAGG[C/T]AAGGTCATGGCCTAG | 55230 |
rs769488695 | snp | C/T | 2.62864e-05 | 0.00362526 | intron-variant | USP40 | GRCh38.p7 | 2:233511699 | TTTGAAACAGGTGAC[C/T]TTATTTTACCTGAGA | 55230 |
rs769498805 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233551953 | CAAAAATTATACATG[A/C]ATATGTATTTTTCTG | 55230 |
rs769519889 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233498362 | TGTCAGAAATGTTCC[C/T]ACTGCACTGTGACTT | 55230 |
rs769537210 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233554580 | AGAGGTTTACAAACA[C/T]ATCATCAACTCACAT | 55230 |
rs769537309 | snp | C/G | 1.69686e-05 | 0.00291273 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233498606 | TTTCGTAAATGCCAG[C/G]CATCTCCTATAAAGG | 55230 |
rs769569975 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233501903 | CAGAATGCTCAAAGA[C/T]AGAGAAGAGGAGGAG | 55230 |
rs769643718 | snp | C/T | 0.000289776 | 0.0120334 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233549147 | TCTTTAATATATACA[C/T]GGTAATGGCCTCCGT | 55230 |
rs769660171 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233560642 | CTAAGAAGTACAAAT[C/T]TGAGCCTGAACATGG | 55230 |
rs769661919 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233546568 | GCACTTCCTAAGACT[A/G]AAGAGAGACACGGCA | 55230 |
rs769680626 | in-del | -/TTGC | | | intron-variant | USP40 | GRCh38.p7 | 2:233530749 | TCTTCTTTTTGTAAA[-/TTGC]TTATTTATATCATTT | 55230 |
rs769730299 | snp | G/T | 1.65605e-05 | 0.0028775 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523331 | TGCTGGGATTGCTAA[G/T]GCTGTGAGGACAGTG | 55230 |
rs769730512 | snp | C/T | 9.63809e-05 | 0.00694126 | intron-variant | USP40 | GRCh38.p7 | 2:233561064 | ATATTTGATAATTAA[C/T]AAAATTATTGCTTTG | 55230 |
rs769740371 | in-del | -/AATAT | 6.30577e-05 | 0.0056147 | intron-variant | USP40 | GRCh38.p7 | 2:233549250 | AGAAAAAAGAACAAA[-/AATAT]TGATATAGTTTTCAT | 55230 |
rs769755762 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233480037 | GCAGCCAGTGATCAT[A/G]TCAACGCGTCCCCCT | 55230 |
rs769809527 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233508550 | ATAAGGGCATGGGTA[C/T]TGTTCTGAATTTCTA | 55230 |
rs769867493 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233544102 | TCCCTAGGGTACTCA[A/C]ACTTCTGCCTGGCTG | 55230 |
rs769871726 | snp | A/G | 1.73688e-05 | 0.00294688 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485522 | TAAATTTGCTGTTAA[A/G]CAACTTACCTTAACA | 55230 |
rs769883236 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233508897 | AATTTTTATTATTTT[C/T]CTCAGTCAAGTTCAA | 55230 |
rs769896435 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233480426 | ATGGAGCTGATGCCA[C/T]GGGCAGGTCCTGGGA | 55230 |
rs769935997 | snp | C/T | 0.00012288 | 0.00783741 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233512528 | ATCAAGAAAGACAGA[C/T]GAGTATAAGCCACCT | 55230 |
rs769959287 | snp | G/T | 2.75054e-05 | 0.00370836 | intron-variant | USP40 | GRCh38.p7 | 2:233527611 | AATACATAAATACTG[G/T]GTTTTTATAACAGAC | 55230 |
rs769970033 | snp | A/T | 1.70942e-05 | 0.00292349 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527531 | TGATACTGAGGGCCC[A/T]GGTGAAGATGCAATT | 55230 |
rs769982581 | snp | A/G | 3.65544e-05 | 0.00427503 | intron-variant | USP40 | GRCh38.p7 | 2:233488218 | TGTGTGTCACTTCAG[A/G]TGCACAGGAGAATTT | 55230 |
rs770013526 | snp | A/G | 0.000107718 | 0.00733808 | splice-donor-variant | USP40 | GRCh38.p7 | 2:233499877 | CATGGTAAGTAACTT[A/G]CCTTGTAGGCCAGAT | 55230 |
rs770028535 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233523667 | TCTTTTGAAACTTTC[C/T]TATCTTTTATTTTTT | 55230 |
rs770028817 | in-del | -/GCCAGGTGTG | | | intron-variant | USP40 | GRCh38.p7 | 2:233538882 | AAAAAAGAACACATA[-/GCCAGGTGTG]GCCAGGTGTGGCCAG | 55230 |
rs770043932 | snp | A/G | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233487147 | CACACAAATTCCAAG[A/G]GAGCTTTTCCTTTAG | 55230 |
rs770056056 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233478338 | CTGCGTCCTCAACAC[A/T]CGAGTCTTTCCCACT | 55230 |
rs770132312 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233521911 | CTAAAACATTTAGCA[A/C]TTACTGTGTGTACTT | 55230 |
rs770152304 | snp | A/G | 1.65734e-05 | 0.00287862 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233540752 | CAGCTGATCAACAGG[A/G]ATTAGATTATTCTCC | 55230 |
rs770184251 | snp | A/G | | | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233529642 | TAGCTGTGTGAATAC[A/G]AATTTTCTCAGGATC | 55230 |
rs770196656 | snp | C/T | 1.65663e-05 | 0.002878 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556971 | AAGAAGTTTCCAAAG[C/T]GCTGAAGAGGATTCG | 55230 |
rs770213449 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233517172 | TCACATTCAGTAGAA[A/T]GGCCATGTTGGTGTG | 55230 |
rs770236373 | snp | C/T | 1.68179e-05 | 0.00289977 | intron-variant | USP40 | GRCh38.p7 | 2:233524486 | TTCTTCAGTAATTTT[C/T]TTTACCTCCACCCCA | 55230 |
rs770271540 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233545008 | ATCTTTCTTGGAAGA[A/G]GGCACTTTTAACTCA | 55230 |
rs770298102 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233483547 | TTTCTTATGTCTTCT[A/G]AAGATTGAAAATGAG | 55230 |
rs770300560 | snp | A/C | 3.57545e-05 | 0.004228 | intron-variant | USP40 | GRCh38.p7 | 2:233493372 | AGAGCACAGGCAGTC[A/C]ATTTACTTCTCTTTA | 55230 |
rs770317075 | snp | A/G | 7.49372e-05 | 0.0061207 | intron-variant | USP40 | GRCh38.p7 | 2:233489347 | GAGGGACAGTGTTGC[A/G]TCCAGCAAGGAACCT | 55230 |
rs770359671 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233554353 | ACAAAGTGGGGACCC[C/T]GGGAAAAAGCAGTTA | 55230 |
rs770370938 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233531286 | TATAAATATGTTTTT[A/G]CTGATACAGCAAATT | 55230 |
rs770388676 | snp | G/T | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233487735 | AATAATTATTGACTA[G/T]GACATGGGCACAATT | 55230 |
rs770429176 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233551189 | CATCCAGTAGGTAGA[A/G]GGCAGGGATGCTGCT | 55230 |
rs770473025 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233501077 | GTTTAGAAAATGATG[A/G]TAAAAACACAGTATA | 55230 |
rs770500629 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233489701 | GCACTGAAATCACCT[A/T]GAGAAAGAAGTGAGT | 55230 |
rs770513665 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233500771 | AATACATGCAAAGTG[A/T]TCCCATTTATAATTT | 55230 |
rs770536852 | snp | A/C | 3.15184e-05 | 0.00396966 | intron-variant | USP40 | GRCh38.p7 | 2:233511670 | AATTCTGGTTATGGA[A/C]GGGTTGATTTTGTTT | 55230 |
rs770543755 | snp | A/G | | | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233549163 | GGTAATGGCCTCCGT[A/G]GCAGCCACCTTTGTG | 55230 |
rs770592226 | in-del | -/CC | | | intron-variant | USP40 | GRCh38.p7 | 2:233563360 | CTAGGTGATGTGCCA[-/CC]CCCAATGGGGCATAC | 55230 |
rs770609404 | snp | C/T | 1.77212e-05 | 0.00297663 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485515 | AAAGTGGTAAATTTG[C/T]TGTTAAACAACTTAC | 55230 |
rs770626817 | snp | C/T | 8.94294e-05 | 0.00668631 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233510070 | CACAGATATTGTTTC[C/T]TCTACTACGATTTCC | 55230 |
rs770626877 | snp | C/T | 1.65754e-05 | 0.00287879 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233525535 | TTGCAACACTAAGAA[C/T]CATGTCTCCTTCCCA | 55230 |
rs770669789 | in-del | -/CTTAGTATATTATTTTC | 3.46873e-05 | 0.00416443 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233512648 | AGGAATATTATTTTT[-/CTTAGTATATTATTTTC]CTTAGAGAGCTAGGA | 55230 |
rs770681153 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233510724 | ACACTATTTCTTCTA[C/T]TATGATCTCCATCTC | 55230 |
rs770714763 | snp | C/T | 1.69329e-05 | 0.00290967 | intron-variant | USP40 | GRCh38.p7 | 2:233524589 | TCACCAGTGAGACCA[C/T]TCATCATGACCATCA | 55230 |
rs770724802 | in-del | -/T | 1.75139e-05 | 0.00295916 | intron-variant | USP40 | GRCh38.p7 | 2:233498635 | GAGTCAAAATTGGGA[-/T]TAAAAAAAATTCAAA | 55230 |
rs770783986 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233505458 | ACTAAGAAAAAAAGA[G/T]TGAAGACTCAAATAA | 55230 |
rs770794265 | snp | C/T | 5.17478e-05 | 0.00508638 | intron-variant | USP40 | GRCh38.p7 | 2:233559949 | AAACAAACACATTTC[C/T]AAATGAATTCTTTAA | 55230 |
rs770794626 | snp | A/C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233557914 | GCTACCTGGGAGGCC[A/C/G]AGGCAGCAGGATGCC | 55230 |
rs770813847 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233524792 | GATAATCCAAAGGTC[A/C]AGTGTACTTGAGGCA | 55230 |
rs770834936 | snp | A/T | 3.49938e-05 | 0.00418278 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233481286 | ATCATCATCGTCGTC[A/T]ATCAGGAGATTCTAC | 55230 |
rs770839735 | snp | A/G | 1.66109e-05 | 0.00288187 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233554491 | TTCCAAACCGGATAC[A/G]TTTTTGACTGCTACT | 55230 |
rs770840049 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233538928 | CAACTACTCAGGAGG[C/T]TGAGCTAGGAGGATC | 55230 |
rs770852270 | snp | A/G | 3.32851e-05 | 0.00407939 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533488 | CCATACCTTCAGGGG[A/G]TCTCTGCAACTGGGA | 55230 |
rs770875119 | snp | G/T | 0.000184077 | 0.00959191 | intron-variant | USP40 | GRCh38.p7 | 2:233549278 | TTTTCATAAAATGCT[G/T]ATAATAATCAAAAGA | 55230 |
rs770924874 | snp | A/C | 9.36695e-05 | 0.00684295 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233489451 | GGCTGGGGACGGGAC[A/C]CCGAACTCCAGGAAA | 55230 |
rs770932815 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233509088 | CTGTTTGTAGAAAAT[A/G]GTATTTGGCAGCCAT | 55230 |
rs770934579 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233521807 | AATCCCAAATAAAAC[A/G]AAGTATGAAGCACAA | 55230 |
rs770994312 | snp | C/G | 3.36067e-05 | 0.00409905 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527430 | TTGACTGCCGGAGAT[C/G]TCCTAAAGTTTTTCT | 55230 |
rs770997645 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233483734 | GATTAGGGAGGCTCG[A/G]CCGTTAAGTATAATG | 55230 |
rs771018828 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233512916 | AATATTAATAATCAA[C/T]GGAAAAATTACAATC | 55230 |
rs771050382 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233505842 | TATCCTGATTCCAAG[A/C]CCAGATGTAGATTCA | 55230 |
rs771056015 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233477730 | TGGCAGCACGGCATG[G/T]TTCAGGCTCTGGGGC | 55230 |
rs771062536 | in-del | -/A | 1.66971e-05 | 0.00288934 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533483 | TCTTTCCATACCTTC[-/A]GGGGGTCTCTGCAAC | 55230 |
rs771073245 | snp | C/T | 1.66838e-05 | 0.00288818 | intron-variant | USP40 | GRCh38.p7 | 2:233496850 | GGGAAGACAAAAATG[C/T]TTTTTTGTCACTTAT | 55230 |
rs771086885 | snp | C/T | 0.000118438 | 0.00769449 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477409 | ATCTGAAGCTCCCCA[C/T]GTGGATGGAGAGAGA | 55230 |
rs771090541 | snp | A/G | 6.21794e-05 | 0.00557547 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233549137 | ATGATCAACATCTTT[A/G]ATATATACATGGTAA | 55230 |
rs771110733 | snp | A/G | 1.68789e-05 | 0.00290503 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233498597 | CAATCCATTTTTCGT[A/G]AATGCCAGGCATCTC | 55230 |
rs771112404 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233560413 | AGACTGAGCAATGTT[A/G]CTCAGAGTCTGGTCT | 55230 |
rs771113235 | snp | C/G | 1.74142e-05 | 0.00295073 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486001 | GAAAACCGTCAAGCG[C/G]CAGATCCAAACAAAC | 55230 |
rs771171907 | snp | A/G | 1.8394e-05 | 0.0030326 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533727 | TTCTTCAAGAGACGA[A/G]CTGTACTTTCATCTG | 55230 |
rs771174324 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233499621 | CTAATTTACATTCCC[A/T]CCAACACTGTAAAAC | 55230 |
rs771203306 | snp | A/C | 0.000583899 | 0.0170766 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485938 | ATAGGTCCTCTCACC[A/C]GGGATGCGCACCTGT | 55230 |
rs771223335 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233520260 | CCCACATTGTGAAAA[C/G]AAGAAACAGAGTGAG | 55230 |
rs771224578 | snp | A/G | 0.000400761 | 0.0141499 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556878 | CGCTAACGTTCTTAC[A/G]TTCTTTACAAACAAT | 55230 |
rs771258785 | snp | C/T | 5.41506e-05 | 0.00520311 | intron-variant | USP40 | GRCh38.p7 | 2:233493348 | AAATAAATATATCAA[C/T]TGACTCTCAGAGCAC | 55230 |
rs771259821 | snp | C/T | 1.65647e-05 | 0.00287786 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556953 | GACCGGAGGTCCCAA[C/T]TAAAGAAGTTTCCAA | 55230 |
rs771266589 | snp | A/T | | | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485697 | ACTTCTCTATCACTG[A/T]GAAAAATTGCATAAC | 55230 |
rs771272623 | snp | C/T | 9.81884e-05 | 0.00700604 | intron-variant | USP40 | GRCh38.p7 | 2:233561030 | GTATAGGCCAAGTCA[C/T]TTTCTGGAAATAAAG | 55230 |
rs771284445 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543916 | CCCAAAGGAGGGAGT[C/T]GAGGGACTGGTCTTT | 55230 |
rs771288498 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233482406 | TTTCCACTTCATTCT[A/G]TTACCTGTAATGCTT | 55230 |
rs771337794 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233506499 | CAAAAGAACATAGAC[-/A]AAATGGGATTATAGC | 55230 |
rs771342898 | snp | C/T | 0.000175223 | 0.00935847 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233519636 | CTTCATTAATTTTAA[C/T]TCCTTTATGGCTTTA | 55230 |
rs771349240 | snp | A/G | 1.68284e-05 | 0.00290067 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527509 | GTGCAGAGCCCCATT[A/G]AAGAAATGATACTGA | 55230 |
rs771364524 | snp | C/G | 1.88695e-05 | 0.00307155 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533737 | GACGAACTGTACTTT[C/G]ATCTGAACTGAGTAG | 55230 |
rs771381044 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233528169 | TTTTTGGTAGAGATG[C/G]GGTTTCACCATGTTG | 55230 |
rs771424537 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233491920 | TAACTGTCTTTACTG[A/C]TGAGCATGCCACTAA | 55230 |
rs771426460 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233507101 | AATCATAAAGGAAAT[A/G]TAAATCAAAACCACA | 55230 |
rs771434199 | snp | C/G | | | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233568620 | TGAAAGGATTGTCCA[C/G]ACAATACTTTGACAT | 55230 |
rs771436127 | snp | C/G/T | 7.27352e-05 | 0.00603012 | intron-variant | USP40 | GRCh38.p7 | 2:233529392 | CAGATCTTTATTCTC[C/G/T]GGAATACTAGTCAAA | 55230 |
rs771514305 | snp | A/T | 0.000326531 | 0.0127734 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562730 | TAATAATAATAATAA[A/T]AATACCTTTGCATCG | 55230 |
rs771559959 | snp | C/T | 1.82257e-05 | 0.0030187 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485794 | CGGAAGCCACTCGAA[C/T]TTTTCGGGAAAGTAT | 55230 |
rs771584772 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233558598 | TCAGTGGTTGCCAGC[A/G]GCTGAGTTGAGGGGG | 55230 |
rs771595874 | snp | A/T | 1.70095e-05 | 0.00291625 | stop-gained, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477397 | AGCGGCGCGGTTATC[A/T]GAAGCTCCCCACGTG | 55230 |
rs771631562 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233482144 | TGTCGTGTCAAGTAT[C/T]ATAATCTCTATTCTA | 55230 |
rs771635886 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233530027 | CTGGTTTTGAACTCC[G/T]GGCCTCAAGTGATCT | 55230 |
rs771647527 | in-del | -/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233497102 | TTACAGAAGATGAAA[-/T]TTTTAATTAATCCTA | 55230 |
rs771721359 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233478366 | ACTTTAGTGTTGCCA[A/G]TAGGCATGTGGCACT | 55230 |
rs771735332 | snp | A/G | 1.6671e-05 | 0.00288708 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233493432 | GTTCTCACCTTGGCT[A/G]GAAGTGGCTCTCCAA | 55230 |
rs771744567 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233481376 | GGCATGTCTAAAAAA[C/T]TACCTATATTGACAA | 55230 |
rs771781337 | snp | C/T | 1.95379e-05 | 0.00312547 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485723 | ATAACCTCATTGCTA[C/T]GCCGGTAAGCCCCAA | 55230 |
rs771807649 | in-del | -/TA | | | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233568562 | ACAAAGATATAAGAT[-/TA]TATATAAATATAATC | 55230 |
rs771836916 | snp | C/T | 1.65974e-05 | 0.0028807 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233540666 | CCATGTATTACCTTC[C/T]GCAGTGGTCCATGCT | 55230 |
rs771874683 | in-del | -/AA | 1.7836e-05 | 0.00298625 | intron-variant | USP40 | GRCh38.p7 | 2:233498648 | GGATAAAAAAAATTC[-/AA]AGTTAGGTGAGACGT | 55230 |
rs771892359 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233529158 | CATTCAGCCCAACTA[C/T]GTGCTCACTGATTTC | 55230 |
rs771904873 | snp | G/T | 1.7051e-05 | 0.0029198 | intron-variant | USP40 | GRCh38.p7 | 2:233551563 | TTAAAAACAGGGTTA[G/T]ATAAAAGGATACATA | 55230 |
rs771919703 | snp | A/G | 3.28769e-05 | 0.0040543 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233488270 | TCTGAAGGGGCTCTA[A/G]GCAGATCTCAATTCT | 55230 |
rs771934280 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233479358 | TCACAAGGTCAAGAG[A/T]TTGAGACCATCCTGG | 55230 |
rs771940817 | snp | C/T | 3.51729e-05 | 0.00419347 | intron-variant | USP40 | GRCh38.p7 | 2:233529411 | ATACTAGTCAAACTC[C/T]AAAAGCAATTTAAAA | 55230 |
rs771961065 | in-del | -/TAT/TATATT/TATATTATTTTTCTT | 0.000950269 | 0.0217811 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233512653 | TATTATTTTTCTTAG[-/TAT/TATATT/TATATTATTTTTCTT]AGAGCTAGGAATTAA | 55230 |
rs771994772 | snp | C/G | 0.000118603 | 0.00769983 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233565569 | TTGTGAAACTAAATA[C/G]TACCCTTAAAAAAAG | 55230 |
rs772009018 | snp | G/T | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233487540 | CATGTTAGACATGGT[G/T]GAAAGATAACTTTCT | 55230 |
rs772044707 | snp | C/T | 1.85713e-05 | 0.00304718 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551440 | CTAGTTTCCTTGTAG[C/T]GTTCGCATTTCACAA | 55230 |
rs772052340 | in-del | -/GT | | | intron-variant | USP40 | GRCh38.p7 | 2:233478680 | GGCGACAGCCTGGAA[-/GT]GTGTGAGGTGGGCAT | 55230 |
rs772060547 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533519 | TTTCCGATAAAACAA[C/T]ATGTAGGCACTTTCT | 55230 |
rs772061145 | snp | A/T | 5.51374e-05 | 0.0052503 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233510052 | AAAATTACTTACATC[A/T]CTCACAGATATTGTT | 55230 |
rs772106101 | in-del | -/TGTT | | | intron-variant | USP40 | GRCh38.p7 | 2:233536775 | TCAACCAACCATGAA[-/TGTT]TCAAAAACATTAAAA | 55230 |
rs772153180 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233532282 | TTCGTTTGCAAATAA[C/G]TGTAACGTTGTAACT | 55230 |
rs772154176 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233519065 | CATTAAGAAAATAAA[A/G]TCTATAGAGACAGAA | 55230 |
rs772155294 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476343 | TTCCGCTAAGCTGCT[A/G]TCTGGGAAAGTCAAC | 55230 |
rs772156916 | snp | C/T | 3.15492e-05 | 0.0039716 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233559815 | GATCCTCGTACCTCA[C/T]TACTGGTCCACCCAA | 55230 |
rs772163697 | snp | A/G | 2.3368e-05 | 0.00341811 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485872 | TCTCTGCCTCAGGGA[A/G]CCGGCAGTCCCACCC | 55230 |
rs772187367 | snp | G/T | 1.69252e-05 | 0.00290901 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523179 | AGTTACCTGTTATCA[G/T]CATGAGAATCCTGAA | 55230 |
rs772216657 | snp | A/G | 3.64067e-05 | 0.00426638 | intron-variant | USP40 | GRCh38.p7 | 2:233559931 | GATTCGAACCTGAAT[A/G]AGAAACAAACACATT | 55230 |
rs772241874 | snp | A/G | | | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485629 | TTATTTGTTGGTTCT[A/G]TGGGAAAATCAAACA | 55230 |
rs772242831 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233532110 | TTGCAACTCTGTAAC[C/T]ATTTCAGCCTCTGAA | 55230 |
rs772253493 | snp | C/T | 1.65608e-05 | 0.00287752 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523299 | GGACATCCAGCACTG[C/T]TGATGAAGATGACAC | 55230 |
rs772285794 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233565005 | TAGAATAACAAACAC[A/T]TAAGCCAGAGTTATC | 55230 |
rs772308828 | in-del | -/GC | 0.000175362 | 0.00936216 | intron-variant | USP40 | GRCh38.p7 | 2:233549275 | TAGTTTTCATAAAAT[-/GC]TGATAATAATCAAAA | 55230 |
rs772340117 | in-del | -/GAGA | | | intron-variant | USP40 | GRCh38.p7 | 2:233551146 | TTGGTTGTCACAACT[-/GAGA]GAGGGGGAGTGAGGC | 55230 |
rs772371199 | snp | A/T | 2.02657e-05 | 0.00318315 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233511727 | AGACGAACTTGGTGC[A/T]TTTCCAAGACACAGT | 55230 |
rs772435419 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233554820 | ACCACAATAAGACAC[A/G]TATCTGAATTCAGAA | 55230 |
rs772438015 | in-del | -/TGTT | | | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475106 | TTTCTAAATATAAAC[-/TGTT]TATTTAGCATCTGAA | 55230 |
rs772440717 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233484531 | GCCTGGGCTGCAGTG[C/T]AGTGGCACGATCTTG | 55230 |
rs772441326 | snp | C/G | 2.92976e-05 | 0.00382726 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233512547 | TATAAGCCACCTTTT[C/G]AAAGTTATCAAAAAG | 55230 |
rs772516172 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233541346 | GAGTAGGCCCTAAGT[A/C]AATCTGATTGGCATT | 55230 |
rs772527294 | in-del | -/AA | 1.68688e-05 | 0.00290416 | frameshift-variant, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477424 | CGTGGATGGAGAGAG[-/AA]GTTTCCGGGGCTCGG | 55230 |
rs772528723 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233491701 | TTTCAAGAGGAGGCA[C/G]GCCATCTATCTTGTC | 55230 |
rs772529987 | snp | A/T | 3.31625e-05 | 0.00407188 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233510060 | TTACATCTCTCACAG[A/T]TATTGTTTCTTCTAC | 55230 |
rs772555778 | snp | A/G | 3.05385e-05 | 0.00390747 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233549112 | GTACTTGAAACTGCC[A/G]GTTTCCCAAATGATC | 55230 |
rs772561873 | snp | A/G | 3.32563e-05 | 0.00407763 | intron-variant | USP40 | GRCh38.p7 | 2:233525569 | TTCTAACAGCTGAAG[A/G]ATATTAATGAAGGAA | 55230 |
rs772562227 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233520087 | GCATAAATAAAAATG[C/T]ATACTATCAGCCCGA | 55230 |
rs772573300 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233542722 | ATGGTGGTAAAAACA[A/T]CACAATAATCTGCAT | 55230 |
rs772590576 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233505439 | TTGGCAAACCTTTAG[C/T]TAGACTAAGAAAAAA | 55230 |
rs772603358 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233500556 | CACTAGAGCAAAAGA[C/G]AGCAAAAATAAGGAA | 55230 |
rs772696848 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233548839 | GTGTATGCACATGCA[A/C]AAATGTGGCAAAATG | 55230 |
rs772716668 | snp | A/T | 3.29061e-05 | 0.0040561 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233488273 | GAAGGGGCTCTAAGC[A/T]GATCTCAATTCTCCG | 55230 |
rs772802652 | snp | A/T | 1.80419e-05 | 0.00300344 | splice-acceptor-variant | USP40 | GRCh38.p7 | 2:233499917 | ATTAACTTTAAACAC[A/T]GTAAAGAAAAACAAT | 55230 |
rs772822139 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233531922 | AATAGGGTCTGGAGA[A/C]AGGGAACCTAAGGCT | 55230 |
rs772836171 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233552277 | ATGGTAGATTTTCAA[A/G]CAAGCTCTAAAAATG | 55230 |
rs772856348 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233547997 | TATGGAAATTGACAA[C/T]GTGGTATTTGCCCAG | 55230 |
rs772858224 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233563939 | CCTCAGTCCCTTTGA[A/G]GCTACGTTTCTACTT | 55230 |
rs772868028 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233482175 | ATACACTCATATGAT[A/G]AGCCAATATTATAAT | 55230 |
rs772893987 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233477596 | TACACTCCAATTTTA[C/T]AGGCCACAAGGACGT | 55230 |
rs772949033 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233514279 | AAATGCTATGAAGGA[A/G]AAGTACAGGGTGTTA | 55230 |
rs772968309 | snp | A/T | 1.73842e-05 | 0.00294819 | intron-variant | USP40 | GRCh38.p7 | 2:233524472 | ATTATCACGAATATT[A/T]CTTCAGTAATTTTTT | 55230 |
rs772971112 | in-del | -/TTG | 1.69522e-05 | 0.00291132 | cds-indel, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485588 | CCCTTGCAAATAATC[-/TTG]TTTTTTTTTCTTTTT | 55230 |
rs772973959 | in-del | -/TAAC | | | intron-variant | USP40 | GRCh38.p7 | 2:233526596 | TTCAGAAAATTCATT[-/TAAC]TAATTTCTGGGAAAA | 55230 |
rs773031044 | in-del | -/TTTTTTGT | | | intron-variant | USP40 | GRCh38.p7 | 2:233517380 | CTTGCACATGCATGG[-/TTTTTTGT]TTTTTTTTTTTTTTT | 55230 |
rs773033254 | snp | C/T | 4.2e-05 | 0.00458239 | intron-variant | USP40 | GRCh38.p7 | 2:233481190 | GCACATCTGTGCAGA[C/T]CCCAGCAATTACCTT | 55230 |
rs773038823 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233556450 | AATAAACTAAATCCC[A/G]TATTTAATTACAAAT | 55230 |
rs773048612 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233522037 | CGAAATACCTTGCCC[A/G]AGGTCCCACTACAGC | 55230 |
rs773058261 | snp | A/C | 1.77445e-05 | 0.00297858 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523473 | TCAATACCAGTTTGA[A/C]TGTGGACTCCACCAA | 55230 |
rs773073474 | snp | A/C | 3.43183e-05 | 0.00414222 | intron-variant | USP40 | GRCh38.p7 | 2:233533463 | GAAACAAATAGGAAC[A/C]TTTTTCTTTCCATAC | 55230 |
rs773080805 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233498088 | CCTGTGATAAAATTA[C/T]TCCTAAGGCTACCCT | 55230 |
rs773082151 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233477811 | CCGTACTTTTTAAAC[A/G]GAAGAATAACATCCG | 55230 |
rs773086370 | snp | C/T | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233487632 | AGTTCATGATATTTA[C/T]AAAAGGACTTGTAAA | 55230 |
rs773123181 | snp | A/G | 1.71173e-05 | 0.00292547 | stop-gained, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477484 | GGATGTAGCTGCTCT[A/G]CTCATGGAGGGCTTC | 55230 |
rs773136606 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476345 | CCGCTAAGCTGCTGT[C/T]TGGGAAAGTCAACCG | 55230 |
rs773224690 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233537175 | GGTGTGAGCCACCAC[A/G]TCCAGGCTATGTTAG | 55230 |
rs773233717 | in-del | -/AAAT | 4.82486e-05 | 0.00491141 | intron-variant | USP40 | GRCh38.p7 | 2:233519683 | CCATCTAAAACAGAG[-/AAAT]AAAATAATGACTAAG | 55230 |
rs773338269 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233520141 | TAAATGACTTTATTT[C/T]AGATTCTTTCCCTTT | 55230 |
rs773386029 | snp | G/T | 2.15654e-05 | 0.00328363 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233491236 | GTAGAGGAGAGAAAC[G/T]TGCGCAGGCTCGTTC | 55230 |
rs773395764 | snp | C/T | | | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485662 | TTAAATAAGCAAAAC[C/T]CAACCTCAAGTTCTC | 55230 |
rs773401013 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476903 | TGAAAGCAGACCCCA[C/T]TTCTGCCCGCTTCTG | 55230 |
rs773445920 | snp | C/G | 1.66026e-05 | 0.00288115 | intron-variant | USP40 | GRCh38.p7 | 2:233540789 | TGAGAGAAACACAGT[C/G]ACTCAAGAAAATCTG | 55230 |
rs773461230 | snp | A/G | 1.66485e-05 | 0.00288513 | intron-variant | USP40 | GRCh38.p7 | 2:233496837 | AGTGTTGCATCCTGG[A/G]AAGACAAAAATGCTT | 55230 |
rs773461378 | snp | C/G | 2.35585e-05 | 0.00343201 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485873 | CTCTGCCTCAGGGAG[C/G]CGGCAGTCCCACCCT | 55230 |
rs773476476 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233512853 | CAGGCAGTCTTTGTT[C/T]TGTGCAGTAGTGCAA | 55230 |
rs773533814 | snp | A/C | 3.08752e-05 | 0.00392895 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233559817 | TCCTCGTACCTCATT[A/C]CTGGTCCACCCAAAG | 55230 |
rs773574775 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233488885 | GCACTCCAGCCTGGG[C/T]GACAGAGCCAGACCC | 55230 |
rs773587597 | snp | C/T | 2.84483e-05 | 0.00377138 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233512553 | CCACCTTTTGAAAGT[C/T]ATCAAAAAGATTTAC | 55230 |
rs773633114 | snp | C/T | 1.71152e-05 | 0.00292529 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233493490 | GTCTGGTCCTGATGA[C/T]TCTCCCAGTGTCCTG | 55230 |
rs773646376 | snp | A/C | 1.76229e-05 | 0.00296835 | intron-variant | USP40 | GRCh38.p7 | 2:233489527 | CGGTTTTAAAAAGCA[A/C]TCTTCAAAACATACT | 55230 |
rs773669584 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233505634 | TAAATGATGAAGAAA[C/T]AGAAAATCTGAACAG | 55230 |
rs773675758 | snp | C/T | 3.94493e-05 | 0.00444107 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233511739 | TGCTTTTCCAAGACA[C/T]AGTCCCAATGAACTT | 55230 |
rs773677560 | snp | C/T | 1.68972e-05 | 0.0029066 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527413 | CGATATTACCTGAAA[C/T]ATTGACTGCCGGAGA | 55230 |
rs773762780 | snp | A/G | 1.65455e-05 | 0.00287619 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477367 | CCGGAGAGTTCATCG[A/G]GAGTAGAGCCGTGCA | 55230 |
rs773763813 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233528081 | CCTCCTAGGTTCAAG[C/T]GATTCTTCTGCCTCA | 55230 |
rs773772440 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233547711 | GCAAATTCTTTTTTT[A/G]AGAAATATTATAAAA | 55230 |
rs773779458 | in-del | -/CAGA | | | intron-variant | USP40 | GRCh38.p7 | 2:233560150 | TACCTTGATATGGTT[-/CAGA]CAAACATTAAAACTC | 55230 |
rs773874055 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233541370 | TGGCATTATCATAAG[A/C]AGACGAAGTTTGGAC | 55230 |
rs773910265 | snp | C/T | 3.41974e-05 | 0.00413492 | intron-variant | USP40 | GRCh38.p7 | 2:233561115 | TTCTTTAAAAAAAAT[C/T]TTCTGAATACGCTAA | 55230 |
rs773910734 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233514066 | CAACTTAAAAAGTGC[C/T]TTTAAAATACTGTCT | 55230 |
rs773921869 | snp | A/C/G | 3.31616e-05 | 0.00407184 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533616 | AACCAGTGGGGACAG[A/C/G]AGATGCTATTGTTTA | 55230 |
rs773962887 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233505629 | AAGATTAAATGATGA[A/C]GAAATAGAAAATCTG | 55230 |
rs773982551 | in-del | -/TGTGTC | | | intron-variant | USP40 | GRCh38.p7 | 2:233491631 | GTGTGTGTGTGTGTG[-/TGTGTC]TGTCTGTCTGTGTGC | 55230 |
rs774094350 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233480259 | GCGGGGCCAGATCAG[C/G]CTCCTACAGTCATTT | 55230 |
rs774104915 | snp | A/G | 7.33178e-05 | 0.00605422 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533725 | TATTCTTCAAGAGAC[A/G]AACTGTACTTTCATC | 55230 |
rs774118170 | snp | A/T | 1.80166e-05 | 0.00300133 | intron-variant | USP40 | GRCh38.p7 | 2:233551355 | GGAAAAGAAAGAATT[A/T]AAAAATAAAATAGTT | 55230 |
rs774132195 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233549523 | TGTAAGCCAATAAAA[C/T]AATGAAATATGTTAC | 55230 |
rs774132267 | snp | C/T | 1.78188e-05 | 0.00298481 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233499903 | CAGATTTCTTCAGCA[C/T]TAACTTTAAACACTG | 55230 |
rs774159563 | snp | C/T | 6.6357e-05 | 0.0057597 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233488249 | CTTACCCCAAGTTTT[C/T]GCCTTTCTGAAGGGG | 55230 |
rs774168797 | snp | G/T | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486328 | CTTGATAGCCCGGCA[G/T]CTGGCAGGAGGAGAG | 55230 |
rs774211792 | snp | C/T | 3.65544e-05 | 0.00427503 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551437 | CAGCTAGTTTCCTTG[C/T]AGCGTTCGCATTTCA | 55230 |
rs774213620 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233506133 | CAAAACAGCAGGGTA[C/G]TGGCAAAAAGTCTGA | 55230 |
rs774219313 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233520749 | ATGAACTAACTAAAT[A/G]AGTAACTCCCACATT | 55230 |
rs774221617 | snp | C/T | 1.80094e-05 | 0.00300073 | intron-variant | USP40 | GRCh38.p7 | 2:233524453 | GACTTTTAAAACATC[C/T]AAAATTATCACGAAT | 55230 |
rs774225087 | snp | A/T | 1.83209e-05 | 0.00302657 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485808 | ACTTTTCGGGAAAGT[A/T]TTTGGCAATTTCAAT | 55230 |
rs774242033 | in-del | -/A | 8.8574e-05 | 0.00665426 | intron-variant | USP40 | GRCh38.p7 | 2:233498636 | AGTCAAAATTGGGAT[-/A]AAAAAAAATTCAAAG | 55230 |
rs774247365 | snp | C/G | 0.00011842 | 0.0076939 | intron-variant, missense | USP40 | GRCh38.p7 | 2:233487997 | GGGCCATCATGGGGT[C/G]AATATGCACCTGGTG | 55230 |
rs774266134 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233477723 | TTTGCACTGGCAGCA[C/T]GGCATGGTTCAGGCT | 55230 |
rs774269415 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233483732 | TGGATTAGGGAGGCT[C/T]GACCGTTAAGTATAA | 55230 |
rs774285328 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233535351 | AAACTTTTTCTTAAA[A/G]AGCCAGATGGTAAAT | 55230 |
rs774289250 | in-del | -/C | 1.74732e-05 | 0.00295572 | frameshift-variant, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485606 | TTTTTTTTTCTTTTT[-/C]CTCTTGGTTATTTGT | 55230 |
rs774289300 | snp | C/T | 1.73712e-05 | 0.00294708 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527542 | GCCCAGGTGAAGATG[C/T]AATTCAAAAGTATTG | 55230 |
rs774295697 | in-del | -/G | 1.65776e-05 | 0.00287898 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533608 | TTATATCAAACCAGT[-/G]GGGACAGGAGATGCT | 55230 |
rs774340329 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233521969 | TCAAGTCTATGAAGT[C/T]GGCACTAGTTATTAT | 55230 |
rs774398127 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233557732 | CTTCTGCTGAGAACA[C/G]AGAAGTGTCTTCTGG | 55230 |
rs774404487 | snp | A/G | 0.000357974 | 0.0133738 | intron-variant | USP40 | GRCh38.p7 | 2:233559807 | AAAGAGCTGATCCTC[A/G]TACCTCATTACTGGT | 55230 |
rs774409506 | snp | C/T | 1.74272e-05 | 0.00295183 | intron-variant | USP40 | GRCh38.p7 | 2:233498630 | ATAAAGGAGTCAAAA[C/T]TGGGATAAAAAAAAT | 55230 |
rs774444039 | in-del | -/CATA | 0.000165851 | 0.00910484 | intron-variant | USP40 | GRCh38.p7 | 2:233549267 | TATTGATATAGTTTT[-/CATA]AAATGCTGATAATAA | 55230 |
rs774447764 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233518566 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 55230 |
rs774481305 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233479317 | CGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCCAA | 55230 |
rs774503629 | snp | A/G | 2.65256e-05 | 0.00364171 | intron-variant | USP40 | GRCh38.p7 | 2:233493587 | AACTGCTGTGATTAC[A/G]AAGATTAAGTGAAAC | 55230 |
rs774512746 | snp | C/T | 8.28425e-05 | 0.0064354 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556985 | GCGCTGAAGAGGATT[C/T]GATTCAGTTCCTGCA | 55230 |
rs774518487 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233544454 | AACTCAATTTCCTGT[C/G]TCTCTCCCCTCCCCA | 55230 |
rs774535401 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476073 | GCTCTCAGACACGTG[-/T]TGCAGAAGCGACGTG | 55230 |
rs774564711 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233503747 | TTATCACCACTAGAC[C/T]AATCTTACAAGAAAA | 55230 |
rs774568667 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233539792 | TTAAAATAAGAACAG[A/C]TATCAGTGAAATAGA | 55230 |
rs774589206 | snp | A/C | 1.65853e-05 | 0.00287964 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233525552 | ATGTCTCCTTCCCAA[A/C]ATTCTAACAGCTGAA | 55230 |
rs774609153 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233560826 | GTGGGGTGGAGAGGT[C/T]GGTATTGTTGCAAAA | 55230 |
rs774660360 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233530897 | TCTGTTTTAAGGGTT[A/G]TATCACTTTGCCCTA | 55230 |
rs774667692 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233516863 | CTCCGTCTCGAATTG[-/A]AAAAAAAAAAAAAAG | 55230 |
rs774675380 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233495755 | AGTAGGGACACTTGC[C/T]TTTCCTGGCCCAGCT | 55230 |
rs774757012 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233513109 | TACATATAAAGAGTC[A/G]TTTAAGCAGGGCTTG | 55230 |
rs774757577 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233556115 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 55230 |
rs774767593 | snp | C/G | 1.73381e-05 | 0.00294427 | intron-variant | USP40 | GRCh38.p7 | 2:233520952 | AAAATTCTGTTAACT[C/G]AAAATCTATCAGCCA | 55230 |
rs774788211 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233538594 | AAATGAACAAATTCC[C/T]TAAAAACCATAATTT | 55230 |
rs774788970 | snp | C/T | 1.65649e-05 | 0.00287788 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233510096 | TTTCCATTTCTGTCC[C/T]AGGTTGAACGTCACT | 55230 |
rs774794479 | snp | C/G | 7.97607e-05 | 0.00631459 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233542347 | TTCAGATTCACATCT[C/G]GTTTACTTTTTTCCT | 55230 |
rs774819854 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233541322 | AAAACGAGGCTGTTT[C/T]CCATTTTAGAGTAGG | 55230 |
rs774839014 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233489051 | TCAGGAGGAGGATCA[C/G]CTGAATCCAACATTT | 55230 |
rs774843275 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233553563 | ATCCCTGCCATATCA[A/G]AAAGGAGCTGGAATG | 55230 |
rs774876934 | snp | A/G | 1.67033e-05 | 0.00288987 | intron-variant | USP40 | GRCh38.p7 | 2:233525429 | CAGGTGAGCCGGACA[A/G]AAATGTAGATATATA | 55230 |
rs774903663 | snp | C/T | 2.19773e-05 | 0.00331484 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485860 | GAAATCGGCAACTCT[C/T]TGCCTCAGGGAGCCG | 55230 |
rs774911202 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233525224 | AGCTTTTCAAGAAAT[G/T]TTAGTAGAGGTAGCC | 55230 |
rs775035968 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233526625 | GAAAAAACACAAAAA[A/G]GCTAACATTTTCTAT | 55230 |
rs775041029 | snp | C/T | 1.68527e-05 | 0.00290277 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233554383 | ATCTGTCTTTACCTT[C/T]GCTGCTTTAACCAGC | 55230 |
rs775065159 | snp | A/T | 3.3157e-05 | 0.00407154 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533598 | TTAGAATCATTTATA[A/T]CAAACCAGTGGGGAC | 55230 |
rs775114831 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233558409 | GTGGCATATCCATCT[A/G]ATAGAATCTCATTTG | 55230 |
rs775166319 | snp | A/T | 2.22497e-05 | 0.00333532 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233491213 | TCTGAGATCTCTATG[A/T]CTCCCAAGTAGAGGA | 55230 |
rs775168374 | snp | A/G | 1.67047e-05 | 0.00288999 | intron-variant | USP40 | GRCh38.p7 | 2:233481311 | TTCTACATTTCAAAA[A/G]AAGTAATGAGCAGTG | 55230 |
rs775171420 | snp | A/C | 1.68337e-05 | 0.00290114 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233554519 | ACTGTTAGATCTAAG[A/C]AGTCTTCCTGAAATA | 55230 |
rs775232371 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233564803 | AGTTATCTCATGTGG[A/G]TGAATGTTCATACAT | 55230 |
rs775241474 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233488956 | AAGAAAAGAAAGAAA[C/T]GAGAAAGAAAGAAAC | 55230 |
rs775260268 | snp | A/G | 5.37418e-05 | 0.00518344 | intron-variant | USP40 | GRCh38.p7 | 2:233489502 | GAAAAAGAAACAGAC[A/G]TTTCTCCAACGGTTT | 55230 |
rs775272281 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233525184 | TATGTTGTTCAACAA[C/T]ATGTGTCAATATAAA | 55230 |
rs775285625 | snp | A/G | 1.7013e-05 | 0.00291654 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233498608 | TCGTAAATGCCAGGC[A/G]TCTCCTATAAAGGAG | 55230 |
rs775286359 | snp | A/T | 0.000119282 | 0.00772183 | intron-variant, missense | USP40 | GRCh38.p7 | 2:233487966 | AGCTGCGGGTGGGCC[A/T]CTTGCTGACACTTCA | 55230 |
rs775366640 | snp | C/G | 1.72136e-05 | 0.00293369 | intron-variant | USP40 | GRCh38.p7 | 2:233493383 | AGTCAATTTACTTCT[C/G]TTTATGATGCACTGG | 55230 |
rs775371421 | snp | A/G | 1.67716e-05 | 0.00289578 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523450 | CATTTAAAAGTAGAG[A/G]TTCGCAGTCAATACC | 55230 |
rs775417795 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233547658 | ATTATAATTTCTTGG[A/G]AACTAGACACCGGTT | 55230 |
rs775420108 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233532452 | ACATGAGGTGAGCAT[G/T]AAGTGGCCAATGGGA | 55230 |
rs775423383 | snp | C/G | 9.29083e-05 | 0.00681509 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485768 | CCCCACAACTTTACC[C/G]AGCTAGATATCGGAA | 55230 |
rs775436341 | snp | C/T | 3.26536e-05 | 0.00404051 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233549150 | TTAATATATACATGG[C/T]AATGGCCTCCGTAGC | 55230 |
rs775461444 | snp | C/T | 3.31208e-05 | 0.00406931 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523333 | CTGGGATTGCTAAGG[C/T]TGTGAGGACAGTGCC | 55230 |
rs775471035 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233533831 | ATTTAAACAAAAATT[A/T]GATGTGATTAAAAAA | 55230 |
rs775474829 | snp | C/G | 1.65326e-05 | 0.00287507 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477464 | AGGCGTCTCTGCACT[C/G]GAGAGGATGTAGCTG | 55230 |
rs775535031 | in-del | -/GT | | | intron-variant | USP40 | GRCh38.p7 | 2:233479628 | CGTATAGAATTTTAC[-/GT]GTGTGTGTGTGTGTG | 55230 |
rs775543012 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233544221 | TTATTACAAAGGATA[C/T]AAATGAATAGCCAGA | 55230 |
rs775547795 | in-del | -/A | 3.97314e-05 | 0.00445692 | intron-variant | USP40 | GRCh38.p7 | 2:233499836 | GTCAAAAAAATTTTT[-/A]ATTAGGCTTTTAAGT | 55230 |
rs775551240 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233482839 | GCGCCTGGCCATGTG[C/T]GTGGGAGTTCCCACG | 55230 |
rs775577602 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233546576 | TAAGACTGAAGAGAG[A/G]CACGGCAATATTGAA | 55230 |
rs775583200 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233513869 | GAGGGGTGGGGGAAG[A/G]TTGAGTGTTCTGTAT | 55230 |
rs775591415 | in-del | -/GTT | | | cds-indel, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477084 | GCGGTTCACGCACAC[-/GTT]GTGCATTTTCTGGTT | 55230 |
rs775611634 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233507299 | CATAGAACTATCATG[C/T]GATTCACCAATCCCA | 55230 |
rs775639836 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233495546 | ACAGGCATCAGGCAC[C/T]GTGCCTAGCCTACCT | 55230 |
rs775719776 | snp | C/G | 4.97253e-05 | 0.004986 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233540757 | GATCAACAGGAATTA[C/G]ATTATTCTCCTCCTT | 55230 |
rs775757004 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233537766 | TTTCAGACAAAATCT[C/G]AAAGCATTTTTCACC | 55230 |
rs775817470 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233502254 | AGTTAAAAAGGCCAG[A/T]AAAAAACTGGGAAAA | 55230 |
rs775858364 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233544540 | TGGCAACCAGCCTCC[-/A]ATCCTGAGGCATCTA | 55230 |
rs775887004 | in-del | -/A | 0.00158103 | 0.0280716 | intron-variant | USP40 | GRCh38.p7 | 2:233533791 | GAACTACACAGAAAC[-/A]AAAAAAAAAAATGCT | 55230 |
rs775888475 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233476292 | CCAGGTGACAAGCAG[G/T]CTCAGGACATGCGAC | 55230 |
rs775914882 | snp | C/T | 3.35008e-05 | 0.00409259 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527462 | TTATCAAAGGTCAAA[C/T]CCCACACGCTTTCTG | 55230 |
rs775918570 | snp | A/G | 3.6673e-05 | 0.00428196 | intron-variant | USP40 | GRCh38.p7 | 2:233551341 | TCAATCTTGAGAGGG[A/G]AAAAGAAAGAATTTA | 55230 |
rs775934980 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233513571 | AGTTAATATACCATA[C/T]ACCATGGTTGCTGAA | 55230 |
rs775940064 | snp | C/T | 1.67837e-05 | 0.00289682 | intron-variant | USP40 | GRCh38.p7 | 2:233524489 | TTCAGTAATTTTTTT[C/T]ACCTCCACCCCATTC | 55230 |
rs775953964 | snp | C/G | 5.84562e-05 | 0.00540598 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485735 | CTATGCCGGTAAGCC[C/G]CAATTTCTCTGAGAC | 55230 |
rs775957185 | in-del | -/AC | 1.74072e-05 | 0.00295013 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485522 | TAAATTTGCTGTTAA[-/AC]AACTTACCTTAACAC | 55230 |
rs775988173 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233500941 | GTGACTTCTAGAGAA[A/C]GGACTAGAATAGAGT | 55230 |
rs775997182 | snp | C/G | | | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233561199 | TTCAAACAAACCAAG[C/G]TCTTCTGGGCCAAGA | 55230 |
rs776013817 | snp | C/T | 1.65718e-05 | 0.00287848 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233540671 | TATTACCTTCCGCAG[C/T]GGTCCATGCTGTTTT | 55230 |
rs776017248 | in-del | -/TC | 3.37479e-05 | 0.00410765 | frameshift-variant, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477454 | GGGGCCGGGCAGGCG[-/TC]TCTGCACTGGAGAGG | 55230 |
rs776128557 | snp | C/T | 5.0841e-05 | 0.00504162 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233521050 | CTAACTGGCATAAAT[C/T]TTTAACGTGGAGCCA | 55230 |
rs776128874 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233546096 | CTGAGGAAGACCTTG[C/T]TAAGGTGTTAGAGCT | 55230 |
rs776148950 | snp | A/C | 3.9419e-05 | 0.00443936 | intron-variant | USP40 | GRCh38.p7 | 2:233481196 | CTGTGCAGACCCCAG[A/C]AATTACCTTTTCCTT | 55230 |
rs776194181 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233478382 | TAGGCATGTGGCACT[C/G]TCTCGGAGTAGCTTG | 55230 |
rs776194634 | snp | A/G | 9.79384e-05 | 0.00699711 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562819 | CTAAAGAAAAAGGTA[A/G]AATCAGAGATGCAAA | 55230 |
rs776254942 | snp | C/T | | | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475272 | GGTTCAGACGATTCT[C/T]CTGCCTCAGCCTCCC | 55230 |
rs776262564 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233501890 | AAGAACTGGGCAGCA[A/G]AATGCTCAAAGATAG | 55230 |
rs776276057 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233550243 | GTGTACACAAAGATG[C/T]CAAGTGACTTTTTTC | 55230 |
rs776360952 | in-del | -/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233509454 | AATGATAGGTTTTCA[-/T]TTTTTTTCTTTTAAT | 55230 |
rs776375028 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233548421 | TGTGTTATCTAAATC[A/C]ATGCTCATTTTATTT | 55230 |
rs776404472 | snp | C/T | 1.66076e-05 | 0.00288158 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523209 | ATTAAAATTGAGCTT[C/T]CATTTCTGAGCCCTT | 55230 |
rs776418664 | snp | C/T | 3.57993e-05 | 0.00423065 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233481288 | CATCATCGTCGTCAA[C/T]CAGGAGATTCTACAT | 55230 |
rs776421685 | snp | C/T | 3.34085e-05 | 0.00408695 | intron-variant | USP40 | GRCh38.p7 | 2:233496859 | AAAATGCTTTTTTGT[C/T]ACTTATGACTTCTGA | 55230 |
rs776436640 | snp | A/G | 3.31214e-05 | 0.00406935 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523317 | ATGAAGATGACACCT[A/G]CTGGGATTGCTAAGG | 55230 |
rs776473724 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233509134 | GGTACTCTGCTGCTA[C/T]CAGGTTGGTCACTCT | 55230 |
rs776496442 | snp | C/T | 1.82397e-05 | 0.00301985 | intron-variant | USP40 | GRCh38.p7 | 2:233499929 | CACTGTAAAGAAAAA[C/T]AATGTCCAATGTTAG | 55230 |
rs776530773 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233531410 | AAAGTACACCTAGAT[G/T]TTTTGTTGGATCTTT | 55230 |
rs776553739 | snp | A/G | 5.63968e-05 | 0.00530992 | intron-variant | USP40 | GRCh38.p7 | 2:233559954 | AACACATTTCTAAAT[A/G]AATTCTTTAAGTGTT | 55230 |
rs776566522 | in-del | -/CCCGCT | | | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233566911 | AGCGAGCTCACCTTG[-/CCCGCT]CCCGCTCCCGCTCCC | 55230 |
rs776570267 | in-del | -/TC | | | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233565784 | CCCTGGATATGTTAA[-/TC]TGTTTTCTTATGTGT | 55230 |
rs776572363 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233497171 | AGAAGGAATTTCTCA[C/T]GAAAAAAAGGACAAG | 55230 |
rs776589708 | snp | C/T | 1.67835e-05 | 0.0028968 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527442 | GATCTCCTAAAGTTT[C/T]TCTTTTATCAAAGGT | 55230 |
rs776597195 | in-del | -/ATATTACCTGAA | 3.4084e-05 | 0.00412806 | intron-variant | USP40 | GRCh38.p7 | 2:233527400 | AGAGGAAGTAAGGCG[-/ATATTACCTGAA]ATATTGACTGCCGGA | 55230 |
rs776609741 | snp | A/G | 8.30365e-05 | 0.00644293 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533496 | TCAGGGGGTCTCTGC[A/G]ACTGGGATTTCCGAT | 55230 |
rs776659759 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233524839 | GGAGTTAGGCTTAAG[C/T]ATGGAATGGTCCCAA | 55230 |
rs776660309 | in-del | -/TTTTTT | | | intron-variant | USP40 | GRCh38.p7 | 2:233529814 | TTCTTTTTCTTTTTC[-/TTTTTT]TTTTTTTTTTTGAGA | 55230 |
rs776667321 | snp | C/T | 3.18446e-05 | 0.00399015 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233549143 | AACATCTTTAATATA[C/T]ACATGGTAATGGCCT | 55230 |
rs776699725 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233491923 | CTGTCTTTACTGCTG[A/G]GCATGCCACTAATGC | 55230 |
rs776747061 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233520459 | CCCATAATGAATTGA[A/G]ACTACATAAATATAA | 55230 |
rs776754433 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233555149 | AGTGAGCCGAGATTG[C/T]GCCACTGCACTCCAG | 55230 |
rs776793900 | snp | A/G | 5.8971e-05 | 0.00542973 | stop-gained, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233529510 | ATCTTGGATTAGCTC[A/G]AGCTGTGAACAAAAT | 55230 |
rs776802954 | snp | A/G | 1.69755e-05 | 0.00291332 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477401 | GCGCGGTTATCTGAA[A/G]CTCCCCACGTGGATG | 55230 |
rs776809500 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543034 | TTCTACTCATCTTTG[C/G]AGGCCAGGCTCAGAT | 55230 |
rs776820329 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233506686 | GATCACTTGAGTTCA[C/G]TAGTTCAAGACCAGC | 55230 |
rs776841536 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233564145 | ATCCAACCCATTAAA[C/T]TGCTCCTAGGAAGGT | 55230 |
rs776870467 | snp | A/G | 1.6566e-05 | 0.00287797 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556967 | ACTAAAGAAGTTTCC[A/G]AAGCGCTGAAGAGGA | 55230 |
rs776873227 | snp | A/G | 0.000116968 | 0.00764658 | intron-variant | USP40 | GRCh38.p7 | 2:233525593 | GAAGGAAAAGAGAAT[A/G]TTGAAAAGTGACATA | 55230 |
rs776879990 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233508565 | TTGTTCTGAATTTCT[A/G]TGTTGTCTGAGTGTT | 55230 |
rs776951115 | snp | A/G/T | 0.000114672 | 0.0075712 | intron-variant | USP40 | GRCh38.p7 | 2:233549054 | ACAAAATAATAGGAA[A/G/T]AGAAAAGAAATTGCA | 55230 |
rs776951431 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233482511 | CTTGGTTGTATCGAC[A/G]GGCATCTGTGTACTA | 55230 |
rs776969759 | in-del | -/AT | | | intron-variant | USP40 | GRCh38.p7 | 2:233485479 | CGTCTCTATAAAATC[-/AT]GTGACCCTCGTGTCT | 55230 |
rs776981404 | snp | A/G | 7.31288e-05 | 0.00604641 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485939 | TAGGTCCTCTCACCA[A/G]GGATGCGCACCTGTG | 55230 |
rs777009270 | in-del | -/A | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233544281 | GGCCCAGAGTTCAGG[-/A]AAACTCTGTTTCCGT | 55230 |
rs777012764 | snp | C/G | 2.27441e-05 | 0.00337217 | intron-variant | USP40 | GRCh38.p7 | 2:233493354 | ATATATCAATTGACT[C/G]TCAGAGCACAGGCAG | 55230 |
rs777023442 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233544046 | TGAGGACTCAGTCCC[A/G]TAAGACTGTTCCCTA | 55230 |
rs777034094 | snp | A/G | 9.75277e-05 | 0.00698243 | intron-variant | USP40 | GRCh38.p7 | 2:233561046 | TTTCTGGAAATAAAG[A/G]GCATATTTGATAATT | 55230 |
rs777074134 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233481625 | CACATCAGCACACGG[A/T]TCTCTCATCGCCGCG | 55230 |
rs777089093 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233515270 | GTAGAATTGGTAAGT[A/G]GATGTTTAAATTTAT | 55230 |
rs777140469 | snp | C/T | 1.92788e-05 | 0.00310468 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533746 | TACTTTCATCTGAAC[C/T]GAGTAGAAATATCTG | 55230 |
rs777140566 | in-del | -/A | 1.72829e-05 | 0.00293959 | intron-variant | USP40 | GRCh38.p7 | 2:233554356 | AGTGGGGACCCTGGG[-/A]AAAAAGCAGTTATCT | 55230 |
rs777157381 | snp | G/T | 1.66701e-05 | 0.002887 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556882 | AACGTTCTTACATTC[G/T]TTACAAACAATCTGG | 55230 |
rs777215314 | snp | C/T | 0.000104644 | 0.00723262 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485893 | AGTCCCACCCTGGGC[C/T]GCGTTCCACACCAGG | 55230 |
rs777236291 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233494093 | AAAGGTGCTATTGTT[A/G]CAGCACTTAATTTCC | 55230 |
rs777254154 | snp | A/G | | | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233565404 | GAAGGGAATTGAGGT[A/G]ACAGGTTCCACCCTG | 55230 |
rs777359604 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233530939 | CTTTGCTTTTATGCT[G/T]AGAAAGGTTTTCTTT | 55230 |
rs777366797 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233538895 | ATAGCCAGGTGTGGC[C/T]AGGTGTGCCTGTGGT | 55230 |
rs777385198 | snp | A/T | 3.16671e-05 | 0.00397901 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233491174 | AGTCTGACCTGAGAC[A/T]TCAGCTCCGCCAGCG | 55230 |
rs777393815 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233483999 | TTTCCACCCTGTCCA[C/T]GAGCCTGTTTGTCTA | 55230 |
rs777399846 | snp | C/T | 1.89878e-05 | 0.00308116 | stop-gained, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233493528 | CTGAAGCTGGTACCA[C/T]CAGATGGGCACCTTC | 55230 |
rs777407462 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233516556 | AGCCGGGCCTGGTGG[C/T]GGGCACCTGTAGTCC | 55230 |
rs777449240 | snp | C/G | 1.68766e-05 | 0.00290483 | intron-variant | USP40 | GRCh38.p7 | 2:233524577 | CCTAGAAAGAGATCA[C/G]CAGTGAGACCATTCA | 55230 |
rs777453557 | snp | C/T | 9.2554e-05 | 0.00680209 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233542268 | ACACACATACTATAC[C/T]TCTAATAAGATTGCT | 55230 |
rs777477484 | snp | C/T | 1.82217e-05 | 0.00301837 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485795 | GGAAGCCACTCGAAC[C/T]TTTCGGGAAAGTATT | 55230 |
rs777496755 | snp | C/T | 0.000135713 | 0.00823638 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233481282 | TGAAATCATCATCGT[C/T]GTCAATCAGGAGATT | 55230 |
rs777543377 | snp | A/T | 1.65726e-05 | 0.00287855 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233540746 | CTGGCCCAGCTGATC[A/T]ACAGGAATTAGATTA | 55230 |
rs777547626 | snp | C/G | 1.65965e-05 | 0.00288062 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233554486 | GCATCTTCCAAACCG[C/G]ATACATTTTTGACTG | 55230 |
rs777585784 | snp | C/G | | | intron-variant, missense | USP40 | GRCh38.p7 | 2:233487776 | GTATTAAGGATATAG[C/G]AATGAATAAACCAAG | 55230 |
rs777600683 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233529211 | CCCTACTTAGCAATG[A/G]CTGTTTTATATGTCA | 55230 |
rs777603049 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233489810 | TGGGAGTAGAATTCA[A/C]CAGGGCAGAGCCCGC | 55230 |
rs777613690 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233536920 | AGACAGGGTCTCATC[C/G]TGTTGCCCAGTCTGC | 55230 |
rs777699422 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233475896 | ACTTACAGCTCTGGC[A/G]TCATCAGAAGCCTCT | 55230 |
rs777753991 | snp | A/C | 2.68741e-05 | 0.00366556 | intron-variant | USP40 | GRCh38.p7 | 2:233511802 | GCTGTCCGGCACTTA[A/C]AAAAATTTTGATAAT | 55230 |
rs777757256 | snp | C/T | 1.65864e-05 | 0.00287974 | intron-variant | USP40 | GRCh38.p7 | 2:233511664 | AGTTATAATTCTGGT[C/T]ATGGAAGGGTTGATT | 55230 |
rs777771652 | snp | A/G | 2.01221e-05 | 0.00317186 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477354 | TTTGTGGCATCAGCC[A/G]GAGAGTTCATCGGGA | 55230 |
rs777773110 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233534720 | TAAGGTACAAAAAAG[C/T]ATCAACAACTTGAAA | 55230 |
rs777836452 | snp | A/G | 1.65616e-05 | 0.00287759 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523304 | TCCAGCACTGTTGAT[A/G]AAGATGACACCTGCT | 55230 |
rs777840988 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533656 | ATTCTGGAGGAAGCA[C/T]CTTGAAAATTTGCTG | 55230 |
rs777847326 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233540678 | TTCCGCAGTGGTCCA[C/T]GCTGTTTTCTGTACT | 55230 |
rs777852856 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543024 | CCTAAGGAAATTCTA[C/T]TCATCTTTGCAGGCC | 55230 |
rs777880208 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233499598 | CACTGTCTTCCACAA[C/T]GGTTGACCTAATTTA | 55230 |
rs777902422 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233515552 | TTCTAAACCTGGGTT[A/C]GGTTACAAGGGTTTT | 55230 |
rs777903053 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233505038 | AAAACTAGAAATCAA[A/G]AAGAAAAACTTTGAA | 55230 |
rs777923863 | snp | A/G | 0.000329797 | 0.012837 | intron-variant | USP40 | GRCh38.p7 | 2:233561021 | ACCCATAGGGTATAG[A/G]CCAAGTCACTTTCTG | 55230 |
rs777940470 | snp | C/T | 1.6566e-05 | 0.00287797 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523407 | TGACAACACTTTTCT[C/T]CATCACTGCTTGTGT | 55230 |
rs778045805 | snp | C/T | 1.92099e-05 | 0.00309913 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527570 | TTGTTTGCAGAATCA[C/T]ATTCTGCCCTTTAAA | 55230 |
rs778046167 | snp | A/C | 3.40866e-05 | 0.00412822 | stop-lost, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477394 | TGCAGCGGCGCGGTT[A/C]TCTGAAGCTCCCCAC | 55230 |
rs778047394 | snp | A/T | 8.77539e-05 | 0.00662339 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233519627 | ACCTAGTTCCTTCAT[A/T]AATTTTAATTCCTTT | 55230 |
rs778096084 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233498075 | AGATTCCAACTCTCC[G/T]GTGATAAAATTATTC | 55230 |
rs778146975 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233522565 | AATATATGGAAATAT[C/T]GCAGTTACAGTGTAT | 55230 |
rs778158878 | snp | A/C/T | 6.74256e-05 | 0.00580594 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477444 | TCCGGGGCTCGGGGC[A/C/T]GGGCAGGCGTCTCTG | 55230 |
rs778160581 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233554962 | CCTTAAGATATACTA[A/C]AGAAGTTATAAGAAA | 55230 |
rs778161330 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233563647 | CATTGTAATGGAGTA[A/C]AATGGAACCCAATGT | 55230 |
rs778207797 | snp | C/T | 0.000193792 | 0.00984167 | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233561178 | TGCATCGGGTTTATC[C/T]TTATCTTCAAACAAA | 55230 |
rs778221761 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233555439 | ACTCATGGTGAAGAT[A/T]TCAAGTACCAAAAGT | 55230 |
rs778240329 | snp | C/T | 3.65337e-05 | 0.00427382 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485790 | ATATCGGAAGCCACT[C/T]GAACTTTTCGGGAAA | 55230 |
rs778246610 | in-del | -/AG | | | intron-variant | USP40 | GRCh38.p7 | 2:233481563 | TGCGAGTGGCCAAAC[-/AG]GGGGACTTTAAAGGG | 55230 |
rs778269165 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233492874 | AACAGAACTCACTGA[C/T]AGTGACTTCTGCCCA | 55230 |
rs778312591 | snp | A/C | | | intron-variant, missense | USP40 | GRCh38.p7 | 2:233487906 | AGAGCGACGGGAGCA[A/C]TGATGAATCCGTTGG | 55230 |
rs778333284 | snp | A/G | 3.81541e-05 | 0.00436756 | intron-variant | USP40 | GRCh38.p7 | 2:233488195 | AAGGCAAACGAGGTT[A/G]AGATACGTGTGTGTC | 55230 |
rs778333393 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543779 | GTTTACAAATTACCC[A/T]GCCTAAGTGTTGTGA | 55230 |
rs778360071 | snp | A/G | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233486856 | GTGAGGCCAAGGCCT[A/G]GAGCCCAGCACAGTG | 55230 |
rs778396353 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233496092 | CAGAGAAAAGGTGTA[A/G]GAGTGATTTCTGCTT | 55230 |
rs778412235 | snp | A/G | 3.02229e-05 | 0.00388723 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233549121 | ACTGCCAGTTTCCCA[A/G]ATGATCAACATCTTT | 55230 |
rs778421171 | snp | A/T | 0.000119185 | 0.00771869 | intron-variant | USP40 | GRCh38.p7 | 2:233499836 | AGTCAAAAAAATTTT[A/T]ATTAGGCTTTTAAGT | 55230 |
rs778421270 | snp | A/G | 1.72484e-05 | 0.00293665 | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233485996 | TACCAGAAAACCGTC[A/G]AGCGCCAGATCCAAA | 55230 |
rs778457928 | in-del | -/T | 1.65611e-05 | 0.00287755 | frameshift-variant, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523368 | CTGCATTAGCTGGAA[-/T]AGACATGTGGAGATT | 55230 |
rs778503151 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543524 | TAACCGCCAATGCAA[C/T]AGTATTAAGAGGTGG | 55230 |
rs778525679 | snp | A/C/G | 6.74315e-05 | 0.00580621 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233521008 | TGTTAACAGTTGCTG[A/C/G]TATTTTAACTTGCTT | 55230 |
rs778569134 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233549820 | TAGAGGCAGTTTAGT[C/G]GAAGAGGTTCTTTCT | 55230 |
rs778572335 | snp | C/T | 1.67108e-05 | 0.00289052 | intron-variant | USP40 | GRCh38.p7 | 2:233557051 | TTTTAGATGTAATTC[C/T]GGGCTTCAGATTTTT | 55230 |
rs778581035 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233529767 | TTTAAGTATACTTTT[A/T]AAAAAGAACACCCAG | 55230 |
rs778662254 | snp | A/G | 4.96989e-05 | 0.00498467 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556942 | GATGAGGTCATGACC[A/G]GAGGTCCCAACTAAA | 55230 |
rs778693643 | snp | C/T | 0.000114279 | 0.00755821 | missense, upstream-variant-2KB, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233565497 | TTAATTTCTTCCCTT[C/T]TCCATACTGATTATT | 55230 |
rs778695280 | in-del | -/T | 0.000273806 | 0.0116974 | intron-variant | USP40 | GRCh38.p7 | 2:233524481 | ATATTTCTTCAGTAA[-/T]TTTTTTTTACCTCCA | 55230 |
rs778730679 | snp | C/T | | | | | GRCh38.p7 | 2:233564980 | TCCAAAAGGTAGATA[C/T]AATTGGTTGGATAAC | 55230 |
rs778731616 | snp | C/T | | | | | GRCh38.p7 | 2:233542596 | GGCGGGAGGACTGCT[C/T]GAGCCCAGGAGGTCA | 55230 |
rs778750177 | in-del | -/TTAGTATATTATTTTTT | 5.25693e-05 | 0.00512659 | | | GRCh38.p7 | 2:233512649 | GGAATATTATTTTTC[-/TTAGTATATTATTTTTT]TTAGAGAGCTAGGAA | 55230 |
rs778765498 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233511292 | AATAAACTGTGTTTC[A/G]TTCAACCTAAAATGC | 55230 |
rs778801069 | snp | A/C | 0.000147319 | 0.00858124 | intron-variant | USP40 | GRCh38.p7 | 2:233510006 | CTCACAGCAAACATA[A/C]AAACACACACAGCCT | 55230 |
rs778837486 | in-del | -/T | | | downstream-variant-500B | USP40 | GRCh38.p7 | 2:233475365 | GACAGGGTTTCACCA[-/T]GTCAGCCAGGCTGGT | 55230 |
rs778880495 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233515136 | TGCTTAAATACACCA[C/T]CATTTGTTCATCCAT | 55230 |
rs778888748 | snp | C/G | 1.6764e-05 | 0.00289512 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233524557 | CACACAGTGTCAGTT[C/G]ATCCCCTAGAAAGAG | 55230 |
rs779039826 | in-del | -/AA | | | intron-variant | USP40 | GRCh38.p7 | 2:233555951 | AACCCCGTCTCTACT[-/AA]AAAAATACAAAAAAT | 55230 |
rs779050164 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233546407 | TGCAAACAGATATTT[C/T]ATGCATCAAAAAACT | 55230 |
rs779067233 | snp | C/T | 1.65616e-05 | 0.00287759 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523283 | CCAACCCTCCCCACC[C/T]GGACATCCAGCACTG | 55230 |
rs779072545 | snp | A/C | 1.65767e-05 | 0.00287891 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533561 | TTGCTGTTCAATATC[A/C]TTTTCCCTGATTGGC | 55230 |
rs779074043 | snp | A/G | 3.16481e-05 | 0.00397782 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551518 | TTACGTAATTTGGCC[A/G]ACTGTTAAAAGAAAA | 55230 |
rs779102794 | snp | C/T | 0.000136374 | 0.00825641 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477365 | AGCCGGAGAGTTCAT[C/T]GGGAGTAGAGCCGTG | 55230 |
rs779106664 | snp | C/T | 3.28866e-05 | 0.0040549 | stop-gained, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233489422 | TTCCTCTCCACCGTC[C/T]AGGCTCTGAGGTGGG | 55230 |
rs779114119 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233511607 | ATGATTTAAGAAAAA[A/G]CTTTTAGAGAAAAAC | 55230 |
rs779155216 | snp | A/T | 5.25463e-05 | 0.00512546 | intron-variant | USP40 | GRCh38.p7 | 2:233523160 | CCTTTTTCTCTTGTT[A/T]GCGAGTTACCTGTTA | 55230 |
rs779173983 | snp | C/T | 0.000132696 | 0.00814436 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233554475 | TGTTCCAGAGAGCAT[C/T]TTCCAAACCGGATAC | 55230 |
rs779182814 | snp | A/G | 2.86357e-05 | 0.00378378 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485920 | CAGGTCCAGGGCAGG[A/G]GCATAGGTCCTCTCA | 55230 |
rs779190891 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233519870 | GGACTTCATAGTTAA[A/G]TTTTTACCAAATTGA | 55230 |
rs779236693 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233510543 | ATGTAGCTGGGATTC[C/T]AGGTGCATGCCACTA | 55230 |
rs779247675 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233522438 | TACTACGAAAGAAAC[A/G]GTCCACAAGTGCTCT | 55230 |
rs779255994 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233500002 | TGGACCCTAGGCCTA[C/T]TTAAGTCTGACTATA | 55230 |
rs779292270 | snp | A/G | 1.70206e-05 | 0.00291719 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485987 | TGGGGGCTGTACCAG[A/G]AAACCGTCAAGCGCC | 55230 |
rs779317511 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233521376 | TAAGTAAACAGTTGC[G/T]GGCTTCTGCCTGCAC | 55230 |
rs779375131 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233530066 | CAGCCTCCCAAAGTG[C/T]TGAGATTAAAGGCAT | 55230 |
rs779388252 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477338 | GCCCAGGAAACCCAC[A/G]TTTGTGGCATCAGCC | 55230 |
rs779447484 | snp | C/T | 0.000120037 | 0.00774622 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556863 | TATTTACCTGCCTCT[C/T]GCTAACGTTCTTACA | 55230 |
rs779459741 | snp | C/T | 8.8743e-05 | 0.0066606 | intron-variant | USP40 | GRCh38.p7 | 2:233519535 | CCCTAAACTGTTTTT[C/T]GTATTCTCCTATATT | 55230 |
rs779462772 | snp | C/T | 1.69726e-05 | 0.00291308 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233498551 | AAATCATCTTACTTC[C/T]TCACATAAAGGCTCT | 55230 |
rs779524159 | in-del | -/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233506919 | GTCTTAAAAAAAAAA[-/T]CTAACAAAGAGTTAA | 55230 |
rs779546630 | snp | A/G | 1.66128e-05 | 0.00288204 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233496801 | AGCAAAGTATCTCCA[A/G]AACATATCAGAAGTT | 55230 |
rs779594607 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233552899 | ATAATGAAGTGACCG[C/T]ATAAATATGTCTCTT | 55230 |
rs779595417 | in-del | -/T | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233563061 | TTTCTGATGTTACTG[-/T]TTTTAGTTTTATGCA | 55230 |
rs779597346 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543626 | CCTGAAGGAGTTTTG[A/T]GTGTCCTTTCTGCCA | 55230 |
rs779610850 | in-del | -/ATAC | 1.7871e-05 | 0.00298918 | intron-variant | USP40 | GRCh38.p7 | 2:233542245 | ATACCATACATACAA[-/ATAC]ATACACACACATACT | 55230 |
rs779620878 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233532743 | GGCCAGGAGTTCAAG[A/G]CCAACCTGGGCAATA | 55230 |
rs779698171 | in-del | -/CTCC | | | intron-variant | USP40 | GRCh38.p7 | 2:233514890 | TCATCCCCCCTAAAA[-/CTCC]CTGTCAATTTGCAGC | 55230 |
rs779699893 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477210 | CCCCCGTGGCTGCCA[C/T]GTGTTGCAGAGCTAA | 55230 |
rs779715291 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233499636 | ACCAACACTGTAAAA[C/T]ATTCCTACTTTGTAC | 55230 |
rs779735225 | snp | A/G | 3.03624e-05 | 0.00389619 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233512530 | CAAGAAAGACAGACG[A/G]GTATAAGCCACCTTT | 55230 |
rs779740504 | snp | A/G | 5.80501e-05 | 0.00538718 | intron-variant | USP40 | GRCh38.p7 | 2:233549239 | TTCACTCTAAAAGAA[A/G]AAAGAACAAAAATAT | 55230 |
rs779752943 | snp | G/T | 1.78439e-05 | 0.00298691 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233499882 | TAAGTAACTTACCTT[G/T]TAGGCCAGATTTCTT | 55230 |
rs779773440 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233511921 | GAAAAATGAGTTGCA[C/T]TTCAGACAAAAGGAT | 55230 |
rs779821437 | snp | A/G | 1.71493e-05 | 0.0029282 | intron-variant | USP40 | GRCh38.p7 | 2:233527391 | TCTGAATTAAGAGGA[A/G]GTAAGGCGATATTAC | 55230 |
rs779842987 | snp | C/T | 4.26694e-05 | 0.00461875 | intron-variant | USP40 | GRCh38.p7 | 2:233523519 | AGACAACCATTAGTA[C/T]AGCTGATATTTGCCA | 55230 |
rs779848110 | in-del | -/TA | 3.32862e-05 | 0.00407946 | intron-variant | USP40 | GRCh38.p7 | 2:233525456 | TATAGAGTGAGTTGC[-/TA]TGTTTTCATATTTAT | 55230 |
rs779883337 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233481923 | GGCGCACCCAGGAAG[A/G]GAAGTGCGTGTCAGG | 55230 |
rs779894063 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233514991 | AAAGTGTCCTATGTA[C/T]GGAACCACACAATGT | 55230 |
rs779909920 | snp | C/T | 1.75332e-05 | 0.0029608 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533710 | CAGCCTGGAGAGAAC[C/T]ATTCTTCAAGAGACG | 55230 |
rs779911983 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233483406 | TAACGTGGGAGGATC[A/G]CTTGAGCCCGTGAGG | 55230 |
rs779982840 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233481081 | GACCCGCCACACTGG[C/T]GTGCTTTGTGTGCAC | 55230 |
rs780021571 | snp | A/G | 1.66352e-05 | 0.00288398 | intron-variant | USP40 | GRCh38.p7 | 2:233540647 | AGGACTTCCCAAAAC[A/G]ATGCCATGTATTACC | 55230 |
rs780039879 | snp | A/G | 1.6696e-05 | 0.00288924 | intron-variant | USP40 | GRCh38.p7 | 2:233493412 | GGCTGCTGAAATCCC[A/G]TTCTGTTCTCACCTT | 55230 |
rs780043627 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233548587 | TTGACACTAGAGTGG[C/G]GGAAAAATTGCCATG | 55230 |
rs780080934 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233492418 | CATGTGTTGTGTACA[G/T]ATGTATTACCAAAAA | 55230 |
rs780102003 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233557604 | GGGCACACCAAGACT[A/G]AGAAGTGGAGAAGAG | 55230 |
rs780110320 | snp | C/T | 3.31351e-05 | 0.00407019 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233556934 | AGACGATAGATGAGG[C/T]CATGACCGGAGGTCC | 55230 |
rs780129150 | snp | C/T | 1.6703e-05 | 0.00288985 | intron-variant | USP40 | GRCh38.p7 | 2:233481154 | AGGAATAAGAGAGAG[C/T]CAGAGAGGGCTCTGT | 55230 |
rs780132016 | snp | C/T | 5.47111e-05 | 0.00522997 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485630 | TATTTGTTGGTTCTA[C/T]GGGAAAATCAAACAT | 55230 |
rs780155018 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233545040 | TCCTCAAATTACTCC[C/T]GTAAATCAAGTTCTT | 55230 |
rs780182433 | snp | C/T | 0.000268492 | 0.0115834 | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562712 | CTAAAACTTAAAGTA[C/T]AATAATAATAATAAT | 55230 |
rs780191595 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233488599 | CATGCCAGTCACTTT[A/G]GGGTGGTAATCAGAA | 55230 |
rs780218768 | snp | C/T | 0.000452123 | 0.0150285 | intron-variant | USP40 | GRCh38.p7 | 2:233488346 | TTGAGTGACATAACA[C/T]TTAATTTTCTTGAAT | 55230 |
rs780227744 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233524400 | CTCCCAAAGTGCTGG[C/G]ATTACAGGCATGAGC | 55230 |
rs780234075 | snp | A/G | | | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523340 | TGCTAAGGCTGTGAG[A/G]ACAGTGCCCACTTCT | 55230 |
rs780241649 | snp | A/G | 1.88742e-05 | 0.00307192 | intron-variant | USP40 | GRCh38.p7 | 2:233499959 | GTTTTCTGTTTCTGA[A/G]TTACAGTTCTAGGAC | 55230 |
rs780291323 | snp | G/T | 2.83274e-05 | 0.00376336 | intron-variant | USP40 | GRCh38.p7 | 2:233527613 | TACATAAATACTGTG[G/T]TTTTATAACAGACAC | 55230 |
rs780312509 | snp | A/C | 4.17807e-05 | 0.0045704 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233493548 | TGGGCACCTTCAGGA[A/C]ACCCTGAAGAATGGA | 55230 |
rs780339996 | in-del | -/ATA | 3.78967e-05 | 0.00435281 | intron-variant | USP40 | GRCh38.p7 | 2:233488308 | AGTTTATATTCCCTG[-/ATA]ATAAGTGAAACAAGA | 55230 |
rs780377509 | snp | C/T | 1.73264e-05 | 0.00294328 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233551419 | CGGAGAGGGAATGTA[C/T]AACAGCTAGTTTCCT | 55230 |
rs780398367 | snp | C/T | 1.79506e-05 | 0.00299583 | intron-variant | USP40 | GRCh38.p7 | 2:233523145 | ATGACTTTTAGAAAT[C/T]CTTTTTCTCTTGTTA | 55230 |
rs780399144 | snp | A/T | 0.000236707 | 0.0108765 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233559915 | GTAACTGTAAAGGGA[A/T]GATTCGAACCTGAAT | 55230 |
rs780400989 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233531988 | AACACCCTAACTTTC[C/T]ATTCCTAAGTAACAC | 55230 |
rs780403061 | snp | C/T | 3.32342e-05 | 0.00407627 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233496782 | AAGTTGTCCTTCAAT[C/T]AAAAGCAAAGTATCT | 55230 |
rs780426626 | snp | C/T | 2.91686e-05 | 0.00381883 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233481252 | TTTCTTTTCCAGTGT[C/T]ATCTCTGATTGTACT | 55230 |
rs780435464 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233497754 | GCTTTGAGGTCCACT[G/T]CTTACTCCAGGCAGT | 55230 |
rs780481333 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233490843 | AAACAATGTAAATAA[A/G]GGGATAAAGTGAATG | 55230 |
rs780487315 | snp | C/T | 7.72111e-05 | 0.00621286 | intron-variant | USP40 | GRCh38.p7 | 2:233559803 | CCTTAAAGAGCTGAT[C/T]CTCGTACCTCATTAC | 55230 |
rs780529470 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233518873 | TATCAATTCATGTTT[A/G]TCCAGGATAAACAAA | 55230 |
rs780657356 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233511410 | AGATGTAAAAATGTG[A/C]GAAAAAGAAGGTGTA | 55230 |
rs780673290 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233551220 | AAACACCCTAATGCA[C/T]GAGACAGTCTCCCAC | 55230 |
rs780690360 | snp | A/G | 3.15224e-05 | 0.00396991 | stop-gained, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233549103 | TTTCTATACGTACTT[A/G]AAACTGCCAGTTTCC | 55230 |
rs780718902 | snp | C/G | | | upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233566903 | AACTGGAGCGGGAGC[C/G]GGAGCGGGCAAGGTG | 55230 |
rs780732343 | snp | G/T | 5.96273e-05 | 0.00545986 | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477357 | GTGGCATCAGCCGGA[G/T]AGTTCATCGGGAGTA | 55230 |
rs780747169 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233519334 | CAGTATAGTACAACA[G/T]GAATACATGGACTAG | 55230 |
rs780779778 | snp | C/T | 3.8575e-05 | 0.00439159 | intron-variant | USP40 | GRCh38.p7 | 2:233511835 | GATGAAGGTTATTAA[C/T]TCCTAGCTCTCTAAG | 55230 |
rs780798911 | snp | C/T | 1.72436e-05 | 0.00293624 | missense, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233485598 | TAATCTTGTTTTTTT[C/T]TCTTTTTCCTCTTGG | 55230 |
rs780801216 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233552706 | GGATGGAAATACATG[C/T]GAAACAGTATAAAAT | 55230 |
rs780801611 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233524730 | TTGTAATTTTTCTTT[-/A]AAAACGTTGTGACAA | 55230 |
rs780856046 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233512055 | TTTCCTACTTAATAA[A/C]AATGACTTGTTCAAA | 55230 |
rs780859756 | in-del | -/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233532020 | GGACCAGAGGCTACT[-/T]TCCTTTGACCTTTTC | 55230 |
rs780862730 | snp | C/T | 1.65762e-05 | 0.00287886 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233525540 | ACACTAAGAACCATG[C/T]CTCCTTCCCAAAATT | 55230 |
rs780869657 | snp | G/T | 3.02714e-05 | 0.00389034 | intron-variant | USP40 | GRCh38.p7 | 2:233511680 | ATGGAAGGGTTGATT[G/T]TGTTTTGAAACAGGT | 55230 |
rs780901880 | snp | C/T | 1.66746e-05 | 0.00288739 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523445 | AAGAACATTTAAAAG[C/T]AGAGGTTCGCAGTCA | 55230 |
rs780905333 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233480862 | GGGTGGTTCTGGAGA[C/T]CTGAGGGTGTGGGAA | 55230 |
rs780906249 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233526145 | TATCTAGTCATTCTC[C/T]ACAATACCATAAGGT | 55230 |
rs780952457 | snp | G/T | 8.16693e-05 | 0.00638968 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233542285 | CTAATAAGATTGCTT[G/T]TAGAATCATCAGTGG | 55230 |
rs780957995 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233516612 | AGAATGGCGTGAACC[C/T]GGGAAGCAAAGGTTG | 55230 |
rs780991833 | snp | C/T | 3.36202e-05 | 0.00409988 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233533688 | TCATTCCTTTGGAAA[C/T]CAGACTCAGCCTGGA | 55230 |
rs781028615 | snp | A/C/G | 1.75733e-05 | 0.00296418 | synonymous-codon, missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527548 | GTGAAGATGCAATTC[A/C/G]AAAGTATTGTTTGCA | 55230 |
rs781047531 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233507561 | ATCATGTTAAGTGAA[C/T]GAAGCCAGGCACAGA | 55230 |
rs781056247 | snp | C/G | 3.34052e-05 | 0.00408674 | missense, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233554507 | TTTTTGACTGCTACT[C/G]TTAGATCTAAGAAGT | 55230 |
rs781079424 | snp | A/G | 1.76107e-05 | 0.00296733 | intron-variant, downstream-variant-500B | USP40 | GRCh38.p7 | 2:233485517 | AGTGGTAAATTTGCT[A/G]TTAAACAACTTACCT | 55230 |
rs781098535 | in-del | -/T | 4.11362e-05 | 0.00453502 | frameshift-variant, intron-variant, utr-variant-5-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233549202 | TGAGAAGAGGTCATA[-/T]TATATATTCTAAGTC | 55230 |
rs781172699 | snp | A/G | 7.28023e-05 | 0.0060329 | intron-variant | USP40 | GRCh38.p7 | 2:233491271 | AAGCACCTTCCAAAG[A/G]ACAGAGCGGGATGTT | 55230 |
rs781259344 | snp | C/T | 6.76087e-05 | 0.00581376 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233498600 | TCCATTTTTCGTAAA[C/T]GCCAGGCATCTCCTA | 55230 |
rs781270713 | in-del | -/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233503144 | AATCAGAAAAATTCA[-/T]TCATAATCTGAATCA | 55230 |
rs781274251 | snp | C/T | 0.000111014 | 0.00744949 | intron-variant | USP40 | GRCh38.p7 | 2:233488215 | ACGTGTGTGTCACTT[C/T]AGATGCACAGGAGAA | 55230 |
rs781288139 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233556218 | AAAGGATCAGTGATG[A/G]ATTCAGTGATAATTG | 55230 |
rs781317727 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233531911 | TGAGGCAGGAGAATA[C/G]GGTCTGGAGACAGGG | 55230 |
rs781334247 | snp | A/T | 0.000187301 | 0.00967551 | intron-variant | USP40 | GRCh38.p7 | 2:233549279 | TTTCATAAAATGCTG[A/T]TAATAATCAAAAGAA | 55230 |
rs781360510 | snp | G/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233537028 | AGCTGGGATTACATG[G/T]GCGCACCACCGCATC | 55230 |
rs781360970 | snp | C/T | 1.89034e-05 | 0.0030743 | intron-variant | USP40 | GRCh38.p7 | 2:233499856 | GGCTTTTAAGTAATA[C/T]GTCATCATGGTAAGT | 55230 |
rs781365772 | snp | A/G | 2.05869e-05 | 0.00320828 | intron-variant | USP40 | GRCh38.p7 | 2:233523512 | CATACCAAGACAACC[A/G]TTAGTACAGCTGATA | 55230 |
rs781424264 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233500379 | AAATATAAAAACTCA[A/C]AAGAATTGTGCAAGC | 55230 |
rs781443847 | snp | C/T | 0.000135213 | 0.0082212 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233521036 | CTTCTCTTCAGATTC[C/T]AACTGGCATAAATTT | 55230 |
rs781479130 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233478188 | ATCCTGGTAGGCACG[C/T]GTCCATGTTTTTGAG | 55230 |
rs781479922 | snp | C/T | 3.33444e-05 | 0.00408303 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233493437 | CACCTTGGCTGGAAG[C/T]GGCTCTCCAAACTCT | 55230 |
rs781508574 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233494588 | AAAAGATTTTTGGCT[A/G]GGCTTGGTGGCTCAC | 55230 |
rs781511778 | snp | C/T | 6.61967e-05 | 0.00575273 | intron-variant, utr-variant-5-prime | USP40 | GRCh38.p7 | 2:233561203 | AACAAACCAAGCTCT[C/T]CTGGGCCAAGAGAAA | 55230 |
rs781531638 | snp | C/T | 1.65726e-05 | 0.00287855 | intron-variant | USP40 | GRCh38.p7 | 2:233527602 | AGGCACAAAAATACA[C/T]AAATACTGTGTTTTT | 55230 |
rs781533677 | in-del | -/AAG | 2.59585e-05 | 0.00360258 | cds-indel, downstream-variant-500B, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233512576 | AGATTTACCTGGACA[-/AAG]AAGCTTCCCATTTCT | 55230 |
rs781545893 | snp | A/G | 1.65627e-05 | 0.00287769 | missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233523386 | ACATGTGGAGATTCT[A/G]TCACCTGACAACACT | 55230 |
rs781553009 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233544978 | ATCTCAGGCTTGTGT[C/T]AGAGACAAACACAAA | 55230 |
rs781565298 | snp | A/C | 1.80117e-05 | 0.00300092 | intron-variant | USP40 | GRCh38.p7 | 2:233523139 | ATTAAAATGACTTTT[A/C]GAAATCCTTTTTCTC | 55230 |
rs781600741 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233496434 | TGTTAAAAACACGGT[A/G]AGTTTCCAACAATGA | 55230 |
rs781678855 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233557308 | CACACACATGGCCAT[A/G]CCACAGAAAGCAGAG | 55230 |
rs781723082 | snp | A/G/T | 6.00659e-05 | 0.00547996 | intron-variant | USP40 | GRCh38.p7 | 2:233477549 | ATGGATGCAGTGGGT[A/G/T]TCAGGGTGAGGGGTT | 55230 |
rs781744225 | in-del | -/CT | 2.46703e-05 | 0.00351206 | intron-variant | USP40 | GRCh38.p7 | 2:233493352 | AAATATATCAATTGA[-/CT]CTCAGAGCACAGGCA | 55230 |
rs781757845 | snp | C/G/T | 3.38594e-05 | 0.00411446 | synonymous-codon, missense, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233527521 | ATTGAAGAAATGATA[C/G/T]TGAGGGCCCAGGTGA | 55230 |
rs781763617 | snp | C/G | 1.68567e-05 | 0.00290312 | synonymous-codon, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477446 | CGGGGCTCGGGGCCG[C/G]GCAGGCGTCTCTGCA | 55230 |
rs781776477 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233488523 | ACATGTAGGTCTGGC[C/T]CTGGGAAGATGGCCA | 55230 |
rs796086334 | in-del | -/TCA | | | intron-variant | USP40 | GRCh38.p7 | 2:233510337 | TAAATTGCTTCATCA[-/TCA]ATGTTTTTTACTCCT | 55230 |
rs796087525 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233555660 | TTTTTTTTTTGAGAC[A/G]GAGCCTTGCTCTGCC | 55230 |
rs796097046 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233555327 | TAGTAATAAGCACTT[A/G]CAATTTGGCAAATTT | 55230 |
rs796194663 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562174 | ATTCCTCAGGGATCT[A/G]GAACTAGAAATACCA | 55230 |
rs796228753 | in-del | -/TATATATATATT | | | intron-variant | USP40 | GRCh38.p7 | 2:233494945 | ATATATATATATATA[-/TATATATATATT]TATATATATATATAT | 55230 |
rs796243717 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233491616 | CTCGTGTGTGTGTGT[C/G]TGTGTGTGTGTGTGT | 55230 |
rs796257785 | snp | C/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233552727 | AGTATAAAATTCAAT[C/G]TTCCCGTGAAAGCTA | 55230 |
rs796262064 | in-del | -/GTGTGTGTGTGTGT | | | intron-variant | USP40 | GRCh38.p7 | 2:233491604 | CCCAACCTGTTCCTC[-/GTGTGTGTGTGTGT]GTGTGTGTGTGTGTG | 55230 |
rs796281223 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233543541 | GTATTAAGAGGTGGG[C/G]TCTTCAGGAGATAAT | 55230 |
rs796293474 | snp | A/G | | | intron-variant, utr-variant-3-prime | USP40 | GRCh38.p7 | 2:233487129 | TCAAAATCATAAAGA[A/G]CTCACACAAATTCCA | 55230 |
rs796319675 | in-del | -/GAAAG | | | intron-variant | USP40 | GRCh38.p7 | 2:233478826 | GGTCAAAAGAGAAAG[-/GAAAG]CTTCTCTGCCCCTAT | 55230 |
rs796345264 | snp | A/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233494950 | TATATATATATATAT[A/T]TATATTTATATATAT | 55230 |
rs796417426 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP40 | GRCh38.p7 | 2:233562484 | AAAACCAAACACCAC[A/T]TATTCTCACTCGTAG | 55230 |
rs796500556 | in-del | -/GTGT | | | intron-variant | USP40 | GRCh38.p7 | 2:233491632 | TGTGTGTGTGTGTGT[-/GTGT]CTGTCTGTCTGTGTG | 55230 |
rs796564697 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233505660 | AACAGGCCAACAAGT[A/G]AGAAAATGCTTTCAG | 55230 |
rs796578430 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233539212 | ATTAATAGAAAAGGC[-/A]AAAAAAAAAAATAAG | 55230 |
rs796591520 | snp | C/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233508497 | AATTAGACCTAGAGG[C/T]TTATTCAGATTCAGG | 55230 |
rs796621719 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233558382 | AGATTAAAAAAAAAA[A/G]ACAAAAAACATGTGG | 55230 |
rs796640640 | snp | C/G | | | missense, intron-variant, upstream-variant-2KB, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233565584 | CTACCCTTAAAAAAA[C/G]TGACATATAAATGCT | 55230 |
rs796789295 | in-del | -/T | | | intron-variant | USP40 | GRCh38.p7 | 2:233565132 | AAATATATTGCTTTA[-/T]TTTTTTTACTAAACA | 55230 |
rs796859244 | snp | A/C | | | intron-variant | USP40 | GRCh38.p7 | 2:233564579 | TTCTTACAATAACCC[A/C]CCTTTTAAATTTAGC | 55230 |
rs796869027 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | USP40 | GRCh38.p7 | 2:233477261 | GGCCTCAGAGGAGCC[A/G]TCCCTGTGCTCAAAG | 55230 |
rs796934042 | in-del | -/T | | | upstream-variant-2KB, intron-variant | USP40 | GRCh38.p7 | 2:233565729 | GCAGCAAGATCTAGA[-/T]TTTTTTTCATCCCTA | 55230 |
rs796947308 | in-del | -/A | | | intron-variant | USP40 | GRCh38.p7 | 2:233533792 | GAACTACACAGAAAC[-/A]AAAAAAAAAATGCTA | 55230 |
rs796989245 | snp | A/G | | | intron-variant | USP40 | GRCh38.p7 | 2:233516857 | GCAAGACTCCGTCTC[A/G]AATTGAAAAAAAAAA | 55230 |