| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs118015634 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | USP10 | GRCh38.p7 | 16:84704407 | ATAAATCTGTTTGCA[A/G]TGGAATTTGCTGGCC | 9100 |
| rs118129199 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | USP10 | GRCh38.p7 | 16:84772980 | TATTTCAGGGATGAA[G/T]GGTGCAGTTTGCCTT | 9100 |
| rs118180450 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84713719 | GAATCAACTGTTAGG[A/T]TCCAGAATTAGAGAG | 9100 |
| rs137886326 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84706977 | TATAAACTCTATAAA[C/T]TGCATAGTTTAGAAA | 9100 |
| rs137916222 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84750283 | CGTGGTGGCTCATGG[C/T]TGTAATCCTAGCTAC | 9100 |
| rs137918266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84704971 | TGCATGTGGAGTGCG[A/G]GCCCAGCACCTGCTA | 9100 |
| rs137948872 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP10 | GRCh38.p7 | 16:84777331 | AAGTTAGTAAAACCC[C/T]CAGGCCCTGCAGATT | 9100 |
| rs137951408 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84773439 | CTGGCACAGCAACCC[C/T]ACCTCATACCTCCTT | 9100 |
| rs138056463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84726343 | ATCTTTTCTCCTTCT[C/T]GCCTTCCTTGGGCTG | 9100 |
| rs138131774 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84738701 | CAACTCCTGAAGGTG[C/G/T]TGGCTTCTTTTGAAT | 9100 |
| rs138173001 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84707665 | CCTAATTTTGCCAGG[A/G]AATGAAGCAGATATT | 9100 |
| rs138175864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84735302 | CTGATGTAACCATAC[A/G]TTTTAGTTGCTACAG | 9100 |
| rs138213874 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780185 | GTTTCTATAGCCCAC[C/T]GTTTTCAGTATCACC | 9100 |
| rs138216257 | snp | C/G | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717511 | CCTTTTTATGTCATT[C/G]GTGCTCAATAAGTGT | 9100 |
| rs138250527 | in-del | -/AT | 0.312593 | 0.242037 | intron-variant | USP10 | GRCh38.p7 | 16:84706914 | TGGAGAAGGAGAAAC[-/AT]ATTTATTACGAGATA | 9100 |
| rs138251432 | in-del | -/AAAC | 0.313251 | 0.241866 | intron-variant | USP10 | GRCh38.p7 | 16:84727460 | GTGTTAGCTTTAAAA[-/AAAC]AAACAAACAAACAAA | 9100 |
| rs138261457 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84741704 | CACGACTGGAATCTT[G/T]CCACCAGTTTGCACA | 9100 |
| rs138295986 | snp | C/T | 0.280785 | 0.248097 | intron-variant | USP10 | GRCh38.p7 | 16:84770599 | AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 9100 |
| rs138341791 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | USP10 | GRCh38.p7 | 16:84762662 | CACCACTGCACTCCA[C/G]CCTGGGTGACGGAAT | 9100 |
| rs138509207 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719841 | TAATTTAAATCTTTG[C/G]AGGGCATGTTTCGAC | 9100 |
| rs138515338 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84746574 | AAAAAATATAGTACA[G/T]ATATGGTATAAAGGA | 9100 |
| rs138523217 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84704395 | CGCACAAAACAGATA[A/C]ATCTGTTTGCAATGG | 9100 |
| rs138528370 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84701562 | ATGAACAAGTAAAAG[C/G]CTCATTATGAATTAA | 9100 |
| rs138529272 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84728495 | CAAGCATGTGCCACC[A/G]CGCCCGGCTAATTTT | 9100 |
| rs138563915 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84726218 | CTGCAGCGCCCCCTA[C/G]TGCCGTGCTGTACTG | 9100 |
| rs138612909 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | USP10 | GRCh38.p7 | 16:84750781 | GAGTGGCCAACTGCC[C/T]GATAAGTTAAAATTC | 9100 |
| rs138616826 | snp | G/T | 0.039522 | 0.134904 | intron-variant | USP10 | GRCh38.p7 | 16:84705234 | TGCCTTGTTTTTTTT[G/T]TTTGTTTTTTTTTTT | 9100 |
| rs138619106 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP10 | GRCh38.p7 | 16:84777464 | ACATGCTGCTGTCAT[A/G]GGTGCTTCCTGCCCT | 9100 |
| rs138627146 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84712254 | CTGTGTACAGAGGCC[C/G]TTGTGGTCCTGTCCT | 9100 |
| rs138650995 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84724458 | AACAGGGAAGTAGAC[A/G]CTCAATTGCAGTACT | 9100 |
| rs138703786 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84763966 | GATTGGTTGCCGTGG[C/T]TCCTAATGTAGACCA | 9100 |
| rs138805320 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | USP10 | GRCh38.p7 | 16:84714874 | ATATCAAAAACAAGT[G/T]CTACATATGAAATGT | 9100 |
| rs138812574 | in-del | -/CTGGCTTTTG | | | intron-variant | USP10 | GRCh38.p7 | 16:84738092 | GTTCTAACAGCTCTC[-/CTGGCTTTTG]TGCCTTGTGAAGTGG | 9100 |
| rs138825737 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84767161 | AGCGAGCTCTTCACC[A/G]CATCTGTTCTGGAAA | 9100 |
| rs138871987 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84731637 | AAAATCCTTTTTTCT[C/T]GAAACTTTCAAAATG | 9100 |
| rs138884146 | snp | A/C/T | 0.0319486 | 0.123029 | intron-variant | USP10 | GRCh38.p7 | 16:84736003 | GGCGTGTCACTTGGA[A/C/T]CTGTGGGTGTGTGAG | 9100 |
| rs138889473 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP10 | GRCh38.p7 | 16:84729619 | TGCTCTTAAACCCTT[A/G]GCACTGACTTCTTAG | 9100 |
| rs138964462 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84747583 | TTTTTTTTTTTTTGA[A/G]ATGCAGTCTCACTCT | 9100 |
| rs138980880 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84764529 | TCACTGCTAGGGAGT[A/G]AGAGAAAAGCCAGCT | 9100 |
| rs139101598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84768955 | CTCAGTTGGGCGAGA[C/T]GGATAGCATTCTGCC | 9100 |
| rs139106421 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718687 | CTTGAACCCAGGAGT[C/T]GGAGGTTGCAGTGAA | 9100 |
| rs139269676 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | USP10 | GRCh38.p7 | 16:84774545 | GCGCGATCTCGGCTC[A/G]CTGCAACCTCTGCCT | 9100 |
| rs139272512 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84724907 | TGAAGTTGAAAGCAC[A/G]CAATGATTGTTCAGT | 9100 |
| rs139292986 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP10 | GRCh38.p7 | 16:84744347 | TTTAAAATTGGCAAA[A/G]TATTACTTGCTTTTT | 9100 |
| rs139306309 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | USP10 | GRCh38.p7 | 16:84773019 | TATTAACAGCTGTGT[A/T]GACTAGCCCAGTTAA | 9100 |
| rs139338093 | snp | C/T | 0.0509274 | 0.151229 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745160 | ATTGTGCCTGACAGT[C/T]CTTTCCCCGGAGCAC | 9100 |
| rs139352643 | snp | C/G | 0.0138799 | 0.0821421 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698976 | ATGGATCTTCCTGTT[C/G]ATCTCCTCTGCTCAG | 9100 |
| rs139374842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84771113 | TCAAAGACTTTGTAA[A/G]TACAGAGAATGATAA | 9100 |
| rs139384830 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84736371 | AGCGCCTCCTGCCAG[C/T]GGAGGGCTGCTTTGT | 9100 |
| rs139404758 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | USP10 | GRCh38.p7 | 16:84774083 | GGTGAAACCCCAACT[C/T]TTCTAAAAACACAAA | 9100 |
| rs139406394 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | USP10 | GRCh38.p7 | 16:84743226 | GGTCGTGACTTCATG[C/G]ATAAACTTGCTGTTA | 9100 |
| rs139417614 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | USP10 | GRCh38.p7 | 16:84764905 | TTTCATAAGATAGGT[C/G]ATAAACAATAACCAC | 9100 |
| rs139431560 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84716431 | TCATCTTCATTCAGC[A/C]AATCTTTATTAGATT | 9100 |
| rs139498907 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84742485 | TATTTCCCTCCCTCG[A/C]CCCCTGCCTTGTAGT | 9100 |
| rs139511455 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84740021 | ATCATAAGCATTTCA[A/T]TGTAGCTGATTTACA | 9100 |
| rs139523392 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP10 | GRCh38.p7 | 16:84742758 | CCATAAGAAGAGGAA[C/T]TGTGCTGGCTAGGAA | 9100 |
| rs139583462 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84771729 | CAAAATTAGCCAGAT[C/G]TGGTGGTGGGAGCCT | 9100 |
| rs139640365 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699504 | CCAAAGGCGTGGCCC[A/C]GGCGCCCAGGCAGGA | 9100 |
| rs139666497 | in-del | -/GGGT | | | intron-variant | USP10 | GRCh38.p7 | 16:84757395 | AGGAGGGAATGAGAG[-/GGGT]GGGGGTGTGTGTGTG | 9100 |
| rs139672971 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84713189 | CAATGCCACCATTCA[C/T]CCACTAGTTATTTAT | 9100 |
| rs139725328 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | USP10 | GRCh38.p7 | 16:84760787 | CCAGGGAGCCCTTAT[A/G]AAAGGCCCTGGGGCT | 9100 |
| rs139728356 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84711039 | TACTCACTTATTTTA[A/G]CGCCGAGTGGAATGG | 9100 |
| rs139729204 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84759808 | ACTCGTATAGCTGAT[A/T]TTCTACTTAGCCATC | 9100 |
| rs139735315 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84710367 | TGATTCTTTAGGCTC[C/T]CCTCCATAGCTGGGA | 9100 |
| rs139757602 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | USP10 | GRCh38.p7 | 16:84757123 | TCTAGCACAGTGTCC[C/G]TCACATGACAGGTGC | 9100 |
| rs139847098 | snp | C/G | 0.00993419 | 0.0697739 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698584 | TTTTTCTTTTCTTTT[C/G]TTTCTTTCTTTCTTT | 9100 |
| rs139905467 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | USP10 | GRCh38.p7 | 16:84756462 | GCCGGGCGTGGTGGT[A/G]CACGTCTGTAATCCC | 9100 |
| rs139910263 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | USP10 | GRCh38.p7 | 16:84753172 | TTTTCATAGCAACAG[A/T]GTCTCACTGTGTGGC | 9100 |
| rs139942611 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84713476 | ACCCGCTATCCTGAC[A/G/T]TGTGTGTCTGGTTCA | 9100 |
| rs139972895 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84752966 | TTTATTTTTTAAAAA[C/T]GTATTTTTTTTTTCT | 9100 |
| rs139973789 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84778745 | TGAGTTGAAATAGCA[C/T]TGGTTTGTGTGATGA | 9100 |
| rs140011763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84739833 | TTTTGTTTATAGTGC[A/G]CTTTCCTCTGCTCTC | 9100 |
| rs140062590 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | USP10 | GRCh38.p7 | 16:84749668 | TCACATTTCTGGACT[A/G]TTTCCCCTATTGTTA | 9100 |
| rs140147479 | snp | C/G | 0.000414838 | 0.0143961 | missense, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84733486 | CAATTCTTTGTGACT[C/G]CTCGATCTTCAGTTG | 9100 |
| rs140179274 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84763320 | AATGATCAAGCCTAT[A/G]AAAAAGCTGAAAGAA | 9100 |
| rs140186829 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84761644 | AGTTTTTACTGAGGG[C/T]TGGTCCCATAGGTAC | 9100 |
| rs140190295 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84761293 | AACCCCTCTTGGATC[A/G]TGCACAGAGATAATG | 9100 |
| rs140220967 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779158 | CTTCCCGCCTCTCTT[C/T]AGTGGCTCTTTAGAG | 9100 |
| rs140249945 | snp | C/T | 0.00905795 | 0.0666853 | utr-variant-5-prime, intron-variant | USP10 | GRCh38.p7 | 16:84704827 | CCCGTCTTGAAACAT[C/T]ATGCCCTGGTTGCCC | 9100 |
| rs140279221 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84777274 | ATGGTGACATGCAGT[A/C]CCCCTTGACATTTTA | 9100 |
| rs140334521 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84768443 | GGAATGAGGGGAAAT[C/G]GGTTTGAGTTATGCC | 9100 |
| rs140340599 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718260 | GTTGCTTGTGAGTTC[A/G]TTTATTTTATTGAGA | 9100 |
| rs140352777 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84716944 | AGTCCAGAGCCATAG[A/C/G]GACAGTCACTGTGAT | 9100 |
| rs140385370 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779993 | GGGGCATGAGTTTGC[A/C]TGCAGAATTAAAATC | 9100 |
| rs140389211 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP10 | GRCh38.p7 | 16:84763895 | GGTTGCCGTGGATCC[A/G]GTGACATTGTGCCTG | 9100 |
| rs140392167 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84714381 | AGTGAGTGGCACAAT[C/T]GTAGCTCACTCCCTG | 9100 |
| rs140413181 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84740760 | TTCTTTGTAAACTAA[G/T]GGGCAGCTGGCATCT | 9100 |
| rs140499045 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | USP10 | GRCh38.p7 | 16:84770439 | TATATGAAATATTTG[C/G]TATATAGAAAATGTC | 9100 |
| rs140506350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719484 | ACTGAAGCCAGAATT[A/G]TTGCAGGTGTGGCCT | 9100 |
| rs140537063 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | USP10 | GRCh38.p7 | 16:84743463 | CTACAAAAAGATTTC[C/T]AGGGGTCCTTTCAAG | 9100 |
| rs140568383 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84727215 | TTATCTTGCTCTGTT[A/T]TGGGCAAAACTAATT | 9100 |
| rs140603290 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741443 | CTGTGTGCTTTGCAC[A/G/T]TGGTGAGCATGCTGC | 9100 |
| rs140634055 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84726424 | TTAGCAGGAACACTG[C/G]TTTTCCCACTTCGTC | 9100 |
| rs140689262 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84705520 | ATAGGCGTGAGCCAC[C/T]ACACCCAGCCACTCC | 9100 |
| rs140692768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84708617 | ATTTTTCTCCATCTT[C/T]TTCAAAATCATGTTT | 9100 |
| rs140742988 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84709045 | AACATTCATTCATTC[A/G]TTTGTTCATTCATTC | 9100 |
| rs140753320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84729728 | GCTCATGCATTTAAG[A/G]ATTAAAATGTGATTC | 9100 |
| rs140774368 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84734280 | AAAAAAAAAATCTTG[C/G]TAACTCTTGGTGTTG | 9100 |
| rs140813803 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP10 | GRCh38.p7 | 16:84776124 | TGTGTCCTAGGAGAT[A/G]GGAGGTGGGATCCCT | 9100 |
| rs140827646 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84726173 | TATTTATTCAAATTT[C/T]CAGAGAGATGAAACT | 9100 |
| rs140829930 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84757721 | AATTTAAAAGTAAAG[C/G]AGACAGTGTGGATTG | 9100 |
| rs140881526 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84738220 | CAGAACAGAATACTG[C/G]GAAGTGTGAAGAGAA | 9100 |
| rs140888500 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84766359 | GCAGCTGGGTGGTCA[G/T]TTGTCACCTGGGAAA | 9100 |
| rs140896633 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84754975 | GCAAAACCCTGTCTC[C/T]AGACTTTGTCCCAGA | 9100 |
| rs140918905 | in-del | -/TTG | 0.0399052 | 0.1355 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718791 | TTTCTTCTTTTAGTT[-/TTG]TTGTTGTTGTTGTTT | 9100 |
| rs140996352 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | USP10 | GRCh38.p7 | 16:84743641 | TGTCCTTCCCTTAAC[C/T]TCAAAATGTGTAACT | 9100 |
| rs141065570 | snp | A/G/T | 0.00597247 | 0.0543191 | intron-variant | USP10 | GRCh38.p7 | 16:84706120 | CTCCTGGCCTCAAGG[A/G/T]ATCCCTTCTGCTTCA | 9100 |
| rs141098957 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84747092 | GGACCATCATACGTG[C/T]GGCTCATTGTTGACC | 9100 |
| rs141127216 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717325 | AGATTAGGAATCCTC[C/T]CTTTTAGAAATTTTG | 9100 |
| rs141178939 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84711525 | TTTGCTGTTGTTGCT[C/T]ATGGATTCGTCAGGT | 9100 |
| rs141190084 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | USP10 | GRCh38.p7 | 16:84769785 | GATGTGTCTGTTTTT[C/G]TCTTTTGCTTCTGCT | 9100 |
| rs141190122 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84738850 | ACTCAGCTGAGGAAG[A/C]CAATCAAGCAGCAGC | 9100 |
| rs141228656 | snp | A/G/T | 0.000219166 | 0.0104663 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745096 | GCCCCCGTCAGTTAC[A/G/T]CCCAGGACTTGTAAC | 9100 |
| rs141243064 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84755478 | ACACGCTGCCCCTGC[A/G]TGCTTCTCACTTCTC | 9100 |
| rs141246504 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84737548 | AGTGCCACAACCCAT[C/T]TGGCATTCCTGCAGG | 9100 |
| rs141272538 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84707415 | GCTATTTTTAAGACA[C/T]GAAAACAGCACAGAC | 9100 |
| rs141289206 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | USP10 | GRCh38.p7 | 16:84766817 | AAGCAAAGATAGGGA[A/G]TTCTTACAACGTAGG | 9100 |
| rs141366025 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | USP10 | GRCh38.p7 | 16:84734895 | CCATTCATTGGGAAC[C/T]CGGCCCTTAGCTGTC | 9100 |
| rs141400820 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | USP10 | GRCh38.p7 | 16:84732584 | CCCGAGCAGCCGGGA[C/G]TACAGGTACACGCCA | 9100 |
| rs141443988 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84762093 | TGATAAGTAACAGAA[A/T]CAAACACTCGTGATG | 9100 |
| rs141461728 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | USP10 | GRCh38.p7 | 16:84762580 | CCTGGAGTCCCAGCT[A/G]CTCGGGAGGCTGAGG | 9100 |
| rs141496650 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84711088 | ATGAGAAACCTGACA[-/T]TTTGCCACTTTGAAG | 9100 |
| rs141499076 | in-del | -/AG | 0.0240643 | 0.107019 | intron-variant | USP10 | GRCh38.p7 | 16:84735812 | TGGAGGGGTATAAAA[-/AG]AGTTTATCAAAATCA | 9100 |
| rs141570529 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | USP10 | GRCh38.p7 | 16:84715999 | TCCTGAGCTTCTTGC[C/T]CTTTGGGTCGTCCCT | 9100 |
| rs141582794 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | USP10 | GRCh38.p7 | 16:84722825 | CCTCCCAAAGTGCTG[A/G]GATTACAGGTGTGAG | 9100 |
| rs141603150 | in-del | -/TTG | 0.356597 | 0.226135 | intron-variant | USP10 | GRCh38.p7 | 16:84744046 | TATATATAGGATTCT[-/TTG]TTGTTGTTGTTGTTG | 9100 |
| rs141630688 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | USP10 | GRCh38.p7 | 16:84701569 | AGTAAAAGGCTCATT[A/G]TGAATTAATGTGTAA | 9100 |
| rs141647472 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698687 | CGCAACCTCCGTCTC[C/T]GGGGTTCAAGTGATC | 9100 |
| rs141666725 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP10 | GRCh38.p7 | 16:84703555 | TTAGTGTTAATTCTT[A/G]AAAGAGATACATTTT | 9100 |
| rs141685369 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84775446 | AACAGAAGACCTTGC[C/T]CAAAGCGAACATTTC | 9100 |
| rs141699404 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84773768 | TTTTATTCTATCCAT[C/T]GGGAAACCTGGAATG | 9100 |
| rs141713323 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP10 | GRCh38.p7 | 16:84724616 | TAGTGAGGGAACAAA[A/G]CTTCTCTTCCTCCTT | 9100 |
| rs141718815 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84777412 | GTGAGGTGAAGATCT[A/C]GGACAGAAGTCTCAA | 9100 |
| rs141721671 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | USP10 | GRCh38.p7 | 16:84729050 | TGATCTGCTCGCCTC[A/G]GCTTCTGGAAGTGAC | 9100 |
| rs141767111 | in-del | -/GGGG | | | intron-variant | USP10 | GRCh38.p7 | 16:84757399 | GGGAATGAGAGGGGT[-/GGGG]GTGTGTGTGTGTGTG | 9100 |
| rs141785013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84700679 | CCTTGGGCTGCTGTT[A/G]CAAAGAAAACTCGAA | 9100 |
| rs141820521 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP10 | GRCh38.p7 | 16:84775880 | CTTCTTTCTCTTTTA[C/T]AGCGTCATCTTTTAT | 9100 |
| rs141825808 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84710067 | TTGAGGTAAGGAGTT[C/T]GAGACCAGTCTGGCC | 9100 |
| rs141849337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84774841 | TTTTCACAACTGTTT[C/T]TGTTTTTAAGTCAGC | 9100 |
| rs141861546 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84773207 | CCAGGTTAAAGGCAT[C/G]TTGCTAAAAGCACAG | 9100 |
| rs141884337 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84735954 | CTTTCATGGGGCGGC[A/G]TGTGGTTGGGCCTGT | 9100 |
| rs141998648 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | USP10 | GRCh38.p7 | 16:84739708 | TTTTTACAAAGAAGT[C/G]AGACAGTTCCCATTC | 9100 |
| rs142016461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84701303 | AAATTAGCTGTAGTT[C/T]AGTTTGCATCAGAAT | 9100 |
| rs142032383 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84768126 | GTGTTTATTCCCTTG[G/T]TTAATCTTAAGGGAA | 9100 |
| rs142033216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84712890 | AGGACACTTAGCAAT[A/G]CAGAGAGAATGCCTT | 9100 |
| rs142039994 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84761581 | CAGACTGTGACCACA[C/T]GTGAAATGCTGCCAA | 9100 |
| rs142041596 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84711365 | CATGGGATCAGCACA[C/T]TCCCCCACAGCTCAG | 9100 |
| rs142045338 | snp | A/C/G | 0.00517822 | 0.0506191 | intron-variant | USP10 | GRCh38.p7 | 16:84710746 | TTGTGATCCTCGAGT[A/C/G]CCCTCTTCTAATACC | 9100 |
| rs142083128 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP10 | GRCh38.p7 | 16:84713868 | TCCCAAGAGAAGGGC[A/G]CCCAAAGCAGAAAGA | 9100 |
| rs142107568 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84736273 | ATAAAATATTGTTTT[C/G]TCTACTTGGGGCCAT | 9100 |
| rs142137456 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84761863 | GGAGAGCCACCCAGG[C/T]CTGCTATGAAAAGTC | 9100 |
| rs142145028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84713920 | GAAGTGCATTTGGGA[C/T]GTGGAGAGTTGTCGG | 9100 |
| rs142177682 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84740460 | TTGTTTCCCATTTGA[A/T]TAAACATTTCTTTGT | 9100 |
| rs142196139 | in-del | -/TA | 0.0372196 | 0.131242 | intron-variant | USP10 | GRCh38.p7 | 16:84706845 | GCGCCGGGCCAAGAC[-/TA]TATATATATTTATTC | 9100 |
| rs142204134 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | USP10 | GRCh38.p7 | 16:84712013 | GCATGAGCCACCGCG[C/T]CCGGTGGCTTTTGCT | 9100 |
| rs142223692 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84703431 | TCTTTTTTAGCTTGT[A/G]ATAGCAGATCCTCCA | 9100 |
| rs142246104 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | USP10 | GRCh38.p7 | 16:84748022 | AGCCAGGCGTGGTGG[C/T]GGGCGCCTGTAGTCC | 9100 |
| rs142341511 | in-del | -/G | 0.00595518 | 0.0542414 | intron-variant | USP10 | GRCh38.p7 | 16:84775273 | TAAAACACTGATGAA[-/G]GGGTTTACAGCTGGG | 9100 |
| rs142372999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84746243 | AGTAGAAACAATTCA[C/T]AATAAAAATAGAAAG | 9100 |
| rs142373988 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84726728 | ATATGAGGGGAAGTG[C/G]TGGAGGGGAATAAAT | 9100 |
| rs142383322 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84756984 | AACCTCTTGAGTCAG[A/G]TGGACCCAGGTTCAC | 9100 |
| rs142444741 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84724428 | AGCACTTTAATAGTA[G/T]AAATAGAATATACAA | 9100 |
| rs142457230 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | USP10 | GRCh38.p7 | 16:84721019 | CTGCCTCAGCCTCTC[A/G]AGTAGCCGGGAGTAC | 9100 |
| rs142461369 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84750337 | AGCTTGAACCGGGGA[A/G]GTGGAGGTTCAGTGA | 9100 |
| rs142487638 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | USP10 | GRCh38.p7 | 16:84733908 | GGTATACTATATTCA[A/G]TTTGTCGTTTATTTT | 9100 |
| rs142510993 | snp | C/T | 0.00935741 | 0.067758 | intron-variant | USP10 | GRCh38.p7 | 16:84772704 | ATGCATACATAAGGT[C/T]GGGAGTGTTCGTGGT | 9100 |
| rs142526964 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | USP10 | GRCh38.p7 | 16:84747808 | CTGACCTCAAGTGAT[C/G]TGCTCGCTTCAGCCT | 9100 |
| rs142569038 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84722628 | GTGCAGTGGTGTGAT[A/C]TTGGCTCACTGAAAC | 9100 |
| rs142628702 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | USP10 | GRCh38.p7 | 16:84765995 | TGGAGCCTAATTTCC[C/T]TTCTGAGGCCTTGCG | 9100 |
| rs142670323 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717286 | TTACATCAGTTTCTC[A/G]GGAGGTCTGCTGCCA | 9100 |
| rs142679367 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84771141 | TAAAGGGATTGTTAT[C/T]TGTAAAGATGCATCT | 9100 |
| rs142741281 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | USP10 | GRCh38.p7 | 16:84724888 | AACCACCCACACCAC[A/C]TTCTGAAGTTGAAAG | 9100 |
| rs142741955 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP10 | GRCh38.p7 | 16:84768536 | TGAAACGTGATCCCA[A/G]GGGCCTCTTTTAGCT | 9100 |
| rs142856501 | snp | A/G | 0.000202242 | 0.0100538 | intron-variant | USP10 | GRCh38.p7 | 16:84764305 | TATTTGCCTTTTCTA[A/G]GGTTTTGCCATGTTG | 9100 |
| rs142860211 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | USP10 | GRCh38.p7 | 16:84715697 | TGGCTTACACCATAA[A/T]CTAGAGATTTAGTGG | 9100 |
| rs142872361 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | USP10 | GRCh38.p7 | 16:84705842 | CTCCTGCCTCAGTCT[C/G]TCAAGTAGCTGGGAT | 9100 |
| rs142889671 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84772490 | TGGATGTGGTGTTAG[C/G]TGTTGCAAGTAAGAC | 9100 |
| rs142898831 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84729648 | AGCCCGTTCCTTTAT[A/T]TCAGTTATAAAATCG | 9100 |
| rs142906245 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | USP10 | GRCh38.p7 | 16:84730591 | GTTTGCCGCTGACTC[A/G]TGCTGAAGCCACTTG | 9100 |
| rs142922340 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84762830 | ACTCTTGGGATTTCA[A/G]CTATGCAAGGGAAAC | 9100 |
| rs143022271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84777939 | GCTGGTGTCTGCTGC[C/T]GGCCAGGCAGACCTG | 9100 |
| rs143024724 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84777024 | CGCCCTTTTGGCCAG[C/G]CTGGAAGCCTATTCT | 9100 |
| rs143101855 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84707339 | ATGTTACTATTCACT[A/G]AAGTTTGTGTGGGGT | 9100 |
| rs143214100 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84712634 | GCAGATTTGCCGTCT[A/G]TAGAAATAGTAATGA | 9100 |
| rs143234385 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84758314 | TGCAAGATATCTTTC[-/T]TATCTAGTGTCTGAG | 9100 |
| rs143237317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84762161 | GATTTTGCTGATGTA[C/T]GTGTAACACAGCTAA | 9100 |
| rs143277554 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719234 | TGAGTAATTATCTCA[A/G]ATTATTTTATAATTT | 9100 |
| rs143306753 | snp | C/T | 0.000965476 | 0.0219501 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744868 | GGATGGAAGTTCTAA[C/T]GTGGAGGCGGAAGTT | 9100 |
| rs143320998 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84742128 | TATATATGTATGGGG[A/T]ACATGAGATATTTTC | 9100 |
| rs143351359 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | USP10 | GRCh38.p7 | 16:84741982 | TATTCTGCTCCCTCC[C/G]ACTACCTCCAGCTGC | 9100 |
| rs143371658 | in-del | -/CTT | 0.0706532 | 0.174169 | intron-variant | USP10 | GRCh38.p7 | 16:84732432 | AATTCTTCTCAATGA[-/CTT]CTTCTTCTTCTTTTT | 9100 |
| rs143399690 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84772112 | GCTGGGGTACAGTGG[C/T]GCGAACTTAGCTCAC | 9100 |
| rs143410390 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84749385 | ACTTGCATTAGTATC[C/T]AACTGTTTCTACTGA | 9100 |
| rs143465900 | snp | C/G | 0.152001 | 0.229992 | intron-variant | USP10 | GRCh38.p7 | 16:84721143 | GTGATCCACCTGCCT[C/G]GGCCTCCCAAAGTGC | 9100 |
| rs143509206 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | USP10 | GRCh38.p7 | 16:84742493 | TCCCTCGCCCCCTGC[A/C]TTGTAGTCCAGTCCT | 9100 |
| rs143518412 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP10 | GRCh38.p7 | 16:84769299 | AAGAGCAAAGTAGGA[C/T]ATAGGGACCCTTAGC | 9100 |
| rs143529051 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718996 | AGGGTTTCACTATGT[A/T]GGTCAAGCTGGTCTC | 9100 |
| rs143535161 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | USP10 | GRCh38.p7 | 16:84772223 | CGCCTGGCTAATTTT[A/G]TATTTTTAGTAGAGA | 9100 |
| rs143540832 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | USP10 | GRCh38.p7 | 16:84778610 | GTGTAGGAGTGTCTG[G/T]GTGAGGCGTGGGACA | 9100 |
| rs143549321 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | USP10 | GRCh38.p7 | 16:84758588 | GCCTTAACAGTATGC[A/G]TTTTCTTTGGCTGTG | 9100 |
| rs143669617 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84743508 | GTTCTCCGCAGTAGA[A/G]CACCGTTCTTTGGGT | 9100 |
| rs143713938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84759183 | AGATCCTTATATGGA[C/T]ATCACAGGACACTTA | 9100 |
| rs143726886 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84709825 | GCAGAGGAACTGTCT[C/G]AAAGCCTGCAGCCTG | 9100 |
| rs143737588 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | USP10 | GRCh38.p7 | 16:84708063 | AGCTTGGGTGACAGA[A/G]CGAGACTCTTACGTC | 9100 |
| rs143764444 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84708474 | AAAAAGGAGGTCTGA[A/T]TCACATTCAGATTCT | 9100 |
| rs143767049 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84767985 | GGTGATGACTCTTAA[A/C]GAGCATGCTGCCTTC | 9100 |
| rs143793581 | in-del | -/TT | | | intron-variant | USP10 | GRCh38.p7 | 16:84768847 | TGATGCTTGTTACTC[-/TT]TGATTTGATCTGGAA | 9100 |
| rs143796266 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84759652 | AATGGAATTGGAGCA[C/T]TGATGATCTGTGTTC | 9100 |
| rs143804801 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | USP10 | GRCh38.p7 | 16:84701126 | AAATCATAACCCTTC[A/G]TGAGCAATTGGGTTT | 9100 |
| rs143833026 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84774872 | AGCTTTTTTCTTTTC[C/T]ATTTTGTAGAGCACC | 9100 |
| rs143839139 | snp | C/T | 0.108048 | 0.20579 | intron-variant | USP10 | GRCh38.p7 | 16:84725568 | ACCATGCCCGGCTAA[C/T]TTTTTTTTGTGTTTT | 9100 |
| rs143878734 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP10 | GRCh38.p7 | 16:84733623 | AGTATGGAGACTAAT[A/G]TGAGAAATGCCTCAA | 9100 |
| rs143879054 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84706172 | ACAGGTGTGAGCCAC[A/C]GCGCCTAGCCTCCCT | 9100 |
| rs143882420 | snp | G/T | 0.0185938 | 0.0946107 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698027 | CCAGAGAGACAACCA[G/T]AAATCACTAGTGAGT | 9100 |
| rs143931445 | in-del | -/A | 0.0573809 | 0.159367 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779320 | TTTTAGAAAATACAC[-/A]AAAAACCCATATTTC | 9100 |
| rs143933624 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84773610 | GACGGGCTTGGCTGC[C/T]GTGCCGGGTTTAGTG | 9100 |
| rs143942147 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84731064 | GGCTTGCTGCAACCT[A/C]CACCTCCCGGGTTCA | 9100 |
| rs144103048 | in-del | -/GTTTTTT | | | intron-variant | USP10 | GRCh38.p7 | 16:84749904 | TTGTTCCATTGGCTG[-/GTTTTTT]TTTTTCAAGTGTGAA | 9100 |
| rs144114901 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP10 | GRCh38.p7 | 16:84775609 | AGGTTGGGTGAGCGC[A/G]CCCCCAGCCGGTGAT | 9100 |
| rs144141914 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699252 | AAGGGGCCAAAACCC[A/C]AGGGTGGACCCACTG | 9100 |
| rs144168149 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84739850 | TTTCCTCTGCTCTCC[A/G]ACCATGGACCTGGTC | 9100 |
| rs144169755 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | USP10 | GRCh38.p7 | 16:84743262 | AATCGTCATCAGTGT[A/T]CTTTTCCAGGAACTT | 9100 |
| rs144170379 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84774337 | CGAACAGCATGCCTC[C/T]GACGGACTCTTGTGT | 9100 |
| rs144175086 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84726376 | ATGGAGGAATGTGTC[C/T]TTATTGCTGAGGGCA | 9100 |
| rs144269869 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84756705 | AGCCTTGTTGGAATC[A/T]TGCTGGAGTTTTCAT | 9100 |
| rs144287398 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84737196 | AGACTTCAGAACATG[A/T]CCTTCCTATAGCCAC | 9100 |
| rs144303173 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | USP10 | GRCh38.p7 | 16:84708318 | AGCCGAGTGTGGTGG[C/T]GGGCACCTTTAATCC | 9100 |
| rs144313011 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | USP10 | GRCh38.p7 | 16:84715743 | ATTCCAGAGGTAGAT[C/G]AGGCTTCAAAGTTGG | 9100 |
| rs144350522 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84765594 | ATTCCTGTTGTGGCA[A/G]ATGGCAGGGTCTTTA | 9100 |
| rs144358897 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP10 | GRCh38.p7 | 16:84763750 | ATCCAGTGGCATTGC[A/G]CCTGTTGTGATTGGT | 9100 |
| rs144433688 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | USP10 | GRCh38.p7 | 16:84763474 | ATACATTTTCCCTGA[A/G]TGATTCAAAGTTAAG | 9100 |
| rs144452008 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP10 | GRCh38.p7 | 16:84720837 | TCTGCCCACCTCGAC[A/G]TCGCAAAGTGCTGGG | 9100 |
| rs144493110 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84711051 | TTAGCGCCGAGTGGA[A/T]TGGTGGAACAGTTGT | 9100 |
| rs144553467 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84757225 | AAGGCCCAGTTCGGT[A/G]TTCCATATTAAGAGA | 9100 |
| rs144555988 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84724653 | TTGTCTGCTTCTGCC[A/G]TTTGTAACACTTAGT | 9100 |
| rs144559679 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84708851 | TATGAAGGACTTTAT[A/G]TCTTTTGTGATTGTT | 9100 |
| rs144571558 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | USP10 | GRCh38.p7 | 16:84728461 | TCCCCTGCCTCAGCC[A/T]CCCGGGTAGCTGGGA | 9100 |
| rs144578809 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84752310 | ACCAACCATGATGAA[C/T]TGAAAAGAAGGCTTC | 9100 |
| rs144588002 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84705521 | TAGGCGTGAGCCACC[A/G]CACCCAGCCACTCCT | 9100 |
| rs144616022 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84726181 | CAAATTTCCAGAGAG[A/C]TGAAACTTTCAGAAT | 9100 |
| rs144616344 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84757903 | AATTAACATTTGTCA[A/G]TTGTAAAGAACGTGC | 9100 |
| rs144639584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751149 | TGTTACAGTTGCCTA[C/T]GGTATTCAGTACACA | 9100 |
| rs144746688 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | USP10 | GRCh38.p7 | 16:84730353 | CGCTGTCTGTACCTA[A/G]AGTTCTTCCTCATTT | 9100 |
| rs144764318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84776431 | CTTCTTTTCTCCCCC[C/T]GATCACAATTCCTCC | 9100 |
| rs144776702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84774715 | GACCTCGTGATCGCC[C/T]GTCTCAGCCTCCCAA | 9100 |
| rs144782490 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | USP10 | GRCh38.p7 | 16:84760625 | GGGTAGAATGGAGTG[C/T]ACTGGGCCTGGAATG | 9100 |
| rs144784971 | snp | C/G/T | 0.0123122 | 0.0775715 | intron-variant | USP10 | GRCh38.p7 | 16:84725431 | TGAGACGGAGTTTTG[C/G/T]TCTTGTTACCCGGGC | 9100 |
| rs144988150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84761751 | GCAAACGGTTTAGGC[A/G]GAATCCCGTATCAGT | 9100 |
| rs144991307 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84757398 | AGGGAATGAGAGGGG[G/T]GGGGGTGTGTGTGTG | 9100 |
| rs144996145 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | USP10 | GRCh38.p7 | 16:84740201 | GAAGTAACGGCATGC[A/G]AAGTTGTATGGATTA | 9100 |
| rs145001799 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | USP10 | GRCh38.p7 | 16:84769859 | CGGTGTGGGGGCAGG[G/T]GTTGAGGCGCAGGTA | 9100 |
| rs145003350 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84769254 | TGGGATGGATCTATC[C/G]TTGGCTTATCTTGTG | 9100 |
| rs145069774 | snp | A/G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84766959 | CCGCCTTTCTTCCCC[A/G/T]GTGCCACCTTTGCTA | 9100 |
| rs145194307 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84737640 | GCAGTGTCATCTGGG[A/C]GTTTGCTGGTGGTCG | 9100 |
| rs145195241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84754676 | TCGATTTAAGGGAAT[A/G]GCTGATGTAGAAACT | 9100 |
| rs145197529 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP10 | GRCh38.p7 | 16:84745790 | TGTGTTAATAGCAAC[A/G]TCTGAAGGATGCCTA | 9100 |
| rs145199444 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84706883 | TGAAGTAGGCTTTCT[G/T]GGTAGATCTGATCAT | 9100 |
| rs145200911 | snp | G/T | 0.0271762 | 0.113356 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699899 | GGATGTCCGCGGCCC[G/T]GCAGGCGCACGCCCA | 9100 |
| rs145228085 | in-del | -/TTCTT | 0.0418186 | 0.138422 | intron-variant | USP10 | GRCh38.p7 | 16:84776417 | TTCCTTTTGACTCTC[-/TTCTT]TTCTCCCCCCGATCA | 9100 |
| rs145229232 | snp | G/T | 0.0256215 | 0.110247 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718896 | CTCCTGGGTTCAAGC[G/T]ATTCTCCTGCCTTAG | 9100 |
| rs145270162 | snp | A/C | 0.000399281 | 0.0141238 | missense, intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84704831 | TCTTGAAACATCATG[A/C]CCTGGTTGCCCTCTC | 9100 |
| rs145332714 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84726426 | AGCAGGAACACTGGT[C/T]TTCCCACTTCGTCTA | 9100 |
| rs145354255 | in-del | -/GGGATGGGGGCCCAGGGGTGAGGGCCTAGCGGTGGGGGCCCAG | | | intron-variant | USP10 | GRCh38.p7 | 16:84776280 | GTGGGTGAGGGCCCA[lengthTooLong]GGGTGAGGGCCCAGT | 9100 |
| rs145378923 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84777328 | GACAAGTTAGTAAAA[A/C]CCCCAGGCCCTGCAG | 9100 |
| rs145384749 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84776810 | CTCCTGAATCCTCAT[A/C]CCCTAACCCATTATT | 9100 |
| rs145423977 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84711110 | ACTTTGAAGAGCTGT[C/G]ATGTCGTGTCTTCAG | 9100 |
| rs145428703 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84724924 | AATGATTGTTCAGTA[C/G]ATATCAGCTAGCACC | 9100 |
| rs145440863 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84775453 | GACCTTGCTCAAAGC[A/G]AACATTTCTGTCTTT | 9100 |
| rs145459135 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84713565 | CAGGGGTTTTTGTTT[A/G/T]CTTTGTTCACTGCTG | 9100 |
| rs145489748 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84752979 | AACGTATTTTTTTTT[C/T]CTTAAGAAACAGGGT | 9100 |
| rs145496256 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | USP10 | GRCh38.p7 | 16:84709315 | ACAGTGGGGACAGCA[C/T]GTGTGGTGGACCTTT | 9100 |
| rs145566078 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84743156 | ATTCATTTCCCCTTG[A/G]TATTCTTTTCAAAGT | 9100 |
| rs145604428 | in-del | -/A | | | intron-variant | USP10 | GRCh38.p7 | 16:84754987 | TCTAGACTTTGTCCC[-/A]AGAAAAAAAAAAAAA | 9100 |
| rs145614272 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | USP10 | GRCh38.p7 | 16:84766378 | TCACCTGGGAAACAC[A/C]CAGCCCTGACCACTG | 9100 |
| rs145615429 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717366 | ATGAAATATGTTGAT[G/T]AAATGCCTTTAACAT | 9100 |
| rs145710915 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | USP10 | GRCh38.p7 | 16:84721761 | GGAGTGCAGTGGCGC[C/G]ATCACAGCTCACTGC | 9100 |
| rs145732487 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | USP10 | GRCh38.p7 | 16:84772263 | ACCATGTTGGCCAGG[C/T]TGGTCTCAAACTCTT | 9100 |
| rs145816258 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84725463 | GGAGTGCAAATGGCA[C/T]GATTTCCGCTCACTG | 9100 |
| rs145835528 | in-del | -/GCTG/TTGG | | | intron-variant | USP10 | GRCh38.p7 | 16:84769582 | TGGTTCAGTTGTGCA[-/GCTG/TTGG]TTGTGGGTGACTGTC | 9100 |
| rs145895287 | in-del | -/TGTCACTTGGACCTGTGGGTGTGTGAGTGGCGAGGGCG | | | intron-variant | USP10 | GRCh38.p7 | 16:84736030 | GAGTGGCGAGGGCGT[lengthTooLong]GTCACTTGGACCTGT | 9100 |
| rs145901583 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | USP10 | GRCh38.p7 | 16:84734810 | AGCTGAAATTGAGGC[A/G]CTGAATTTTGTATAT | 9100 |
| rs145960971 | snp | C/T | 0.0607341 | 0.163335 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779794 | AATGAAGATCTCTCC[C/T]TCAGTCTGCTCTGTT | 9100 |
| rs145971296 | in-del | -/A | | | intron-variant | USP10 | GRCh38.p7 | 16:84747554 | TTTTAAAGCCAGGTG[-/A]TTTTTTTTTTTTTTT | 9100 |
| rs145986583 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84761905 | TTGGCTGTGCCAGTT[C/T]TTGCCCTTTTCTGCA | 9100 |
| rs145998836 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | USP10 | GRCh38.p7 | 16:84721043 | GGAGTACAGGTGCCC[A/G]CCACCATGCCTGACT | 9100 |
| rs146003415 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84747851 | GGATTCCAGGTGTGG[A/G]CCACCGCACTCAGGC | 9100 |
| rs146099766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84735985 | GGGTGTGTGAGTGGC[A/G]AGGGCGTGTCACTTG | 9100 |
| rs146117209 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84743037 | GAGCCTTCCGCCCCA[A/C/G]GCACACCCGTTTCAA | 9100 |
| rs146119748 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84764460 | CTCTCCCTGCTGGCG[C/T]ATGTCTGCAGGGGAC | 9100 |
| rs146122282 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | USP10 | GRCh38.p7 | 16:84733210 | TCAAAATAAGCTTTA[G/T]CAGTTTCATAGTGTT | 9100 |
| rs146126424 | snp | A/C/G | 0.000768084 | 0.0195848 | intron-variant | USP10 | GRCh38.p7 | 16:84763110 | TATGGTCCACTTGCC[A/C/G]CAGAGTTGTGCAAGA | 9100 |
| rs146144492 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84761283 | GGTGCTCAGGAACCC[C/G]TCTTGGATCGTGCAC | 9100 |
| rs146214039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84759197 | ACATCACAGGACACT[C/T]ACCCTAGTAACTATT | 9100 |
| rs146243455 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84709827 | AGAGGAACTGTCTCA[A/G]AGCCTGCAGCCTGTT | 9100 |
| rs146243607 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | USP10 | GRCh38.p7 | 16:84774031 | GAGGCAGGCAGATCA[C/T]CTGAGGTCAGGAGTT | 9100 |
| rs146262108 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | USP10 | GRCh38.p7 | 16:84772138 | CTCACTGCAACGTCT[A/G]CCTCCTGGGTTCAAG | 9100 |
| rs146343104 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84712997 | CCAGTGATCTATCTT[C/T]GCAGGCCTGCTTACA | 9100 |
| rs146363424 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84739431 | TGCCTGCCACCACGC[C/G]CAGCTGATTTTTTGT | 9100 |
| rs146366801 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | USP10 | GRCh38.p7 | 16:84736307 | TTGAAAAACCAAAAT[G/T]AAGAAATGTGGGATG | 9100 |
| rs146416884 | in-del | -/ACTC | 0.0107246 | 0.0724382 | intron-variant | USP10 | GRCh38.p7 | 16:84727155 | AGAAACGATGAACTT[-/ACTC]GTGCTTTTTAGTCTC | 9100 |
| rs146418472 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84757511 | GATCTGCCAGTACAA[G/T]GTAGTTTAGAAAAGA | 9100 |
| rs146442833 | snp | A/G | 0.0111196 | 0.0737302 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779362 | TGATTCCTGAGATAA[A/G]AAAGTGGATTTGATC | 9100 |
| rs146488064 | snp | A/T | 0.0836354 | 0.186609 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718830 | AGGAGTCTTTCTCTG[A/T]CACCCAGGCTGGAGT | 9100 |
| rs146495239 | in-del | -/G | 0.106633 | 0.204807 | intron-variant | USP10 | GRCh38.p7 | 16:84704222 | GTACTTCCTGTTAAT[-/G]GTTCCTGGTATTCAG | 9100 |
| rs146510256 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717312 | TGCCACCCAAAAAAG[A/G]TTAGGAATCCTCCCT | 9100 |
| rs146540165 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84769377 | GATCAGTAGAAGTTA[G/T]GCCTAATCTTCTACC | 9100 |
| rs146543718 | snp | C/T | 0.206642 | 0.246211 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84719022 | GTCTCGAACTCCTGA[C/T]CTCAAATGATCCACC | 9100 |
| rs146559017 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84766771 | CTCTGTGTTGAAATT[A/G]GTTGTTGATGTTTCT | 9100 |
| rs146609779 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84730744 | GACCAGCTCTAAAAA[C/G]TTTAGGCTGTATATG | 9100 |
| rs146642608 | in-del | -/AG/GC | | | intron-variant | USP10 | GRCh38.p7 | 16:84733900 | CGTAAATGGTATACT[-/AG/GC]ATATTCAGTTTGTCG | 9100 |
| rs146677005 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | USP10 | GRCh38.p7 | 16:84777245 | TTAACTGGGCTGCTG[C/G]TTATGAAACTAGAAT | 9100 |
| rs146764509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84721342 | ATTAACAAATAGAGC[A/G]TACTGAGGAATTATT | 9100 |
| rs146799989 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84772865 | TCTCATGAAAATGGC[A/C]TGTTGAAAATAGAGG | 9100 |
| rs146850629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84708478 | AGGAGGTCTGATTCA[C/T]ATTCAGATTCTTGTC | 9100 |
| rs146869439 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | USP10 | GRCh38.p7 | 16:84733650 | TCAACCCACCAACTA[G/T]ATTTGACTGACATTT | 9100 |
| rs146869757 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | USP10 | GRCh38.p7 | 16:84706542 | TTTATATATATTTTT[A/T]TATATATATATTTTT | 9100 |
| rs146913960 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP10 | GRCh38.p7 | 16:84720437 | GTGGAGTTTGAGTAC[A/G]TGGTCCGAGAAGCTC | 9100 |
| rs146972440 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | USP10 | GRCh38.p7 | 16:84709683 | GTATAAGGTGTTTCA[A/T]AAAAGGAGGAGAGTG | 9100 |
| rs146989984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84735023 | TATTTTTTTATTTCT[A/G]TTTTTTCTTTTCTTT | 9100 |
| rs147019822 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84732277 | GGAAGCTACTAGACT[A/G]TTTAGTTCCATTAGA | 9100 |
| rs147073149 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84722225 | TTTTGTTTGGTTACC[G/T]TCACCTGACCCAACT | 9100 |
| rs147085878 | in-del | -/AGAA | 0.0383715 | 0.133092 | intron-variant | USP10 | GRCh38.p7 | 16:84731544 | AAAGGTGTATGTGAC[-/AGAA]AGTGTTCTTTCTCTT | 9100 |
| rs147092094 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84746413 | CATCAGAGAGTACTA[C/T]ACAAATACAGGTGGT | 9100 |
| rs147142879 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84716804 | TATATACACCTTACA[A/G]TTACATGGGGAGTGA | 9100 |
| rs147243228 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84777800 | TTTAGTGCTGAAATT[C/T]CCTACCAGCCAAGTC | 9100 |
| rs147245473 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP10 | GRCh38.p7 | 16:84729680 | AAGGACCGGTTTTAA[A/G]TATTGCTGAAGTGTA | 9100 |
| rs147246334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84776032 | GAACCTGTTTGTATC[A/G]TAACATAACACTGCC | 9100 |
| rs147248660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84726464 | GCCCAGGGTTTCTCA[A/G]CTCAGGCCCCCTGAG | 9100 |
| rs147351819 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84742483 | TATATTTCCCTCCCT[C/G/T]GCCCCCTGCCTTGTA | 9100 |
| rs147354865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84771165 | TGCATCTTAGTGACA[A/G]AAAACCTGGCTTTAT | 9100 |
| rs147355310 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84739943 | TCATCTTCGCTAGTG[C/T]ACAAACAAAAGTGTC | 9100 |
| rs147371853 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP10 | GRCh38.p7 | 16:84768820 | ATTGTAAATATAATA[C/T]AGTCATTGTTCTGAT | 9100 |
| rs147409889 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84707658 | AGGTTTACCTAATTT[A/T]GCCAGGGAATGAAGC | 9100 |
| rs147444850 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84708168 | TGTAAAAAGAGGTCT[C/G]GCTGGGCGTGGTGGC | 9100 |
| rs147454561 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84756460 | TAGCCGGGCGTGGTG[G/T]TGCACGTCTGTAATC | 9100 |
| rs147458191 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | USP10 | GRCh38.p7 | 16:84752738 | GTTTTTTTCACTGCG[A/T]GGAAGAAGAGGAGCT | 9100 |
| rs147460724 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84705688 | ATTTGTGTATGTTGA[A/G]TACAGACATAATCAT | 9100 |
| rs147474129 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | USP10 | GRCh38.p7 | 16:84778083 | GGATTTTTTTTTTAA[A/G]TAAATAACTGTGTGT | 9100 |
| rs147578870 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84763592 | ATGACACGGTAATAC[C/T]GACTTTGCAGAGCAT | 9100 |
| rs147595872 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | USP10 | GRCh38.p7 | 16:84713864 | AGGGTCCCAAGAGAA[C/G]GGCGCCCAAAGCAGA | 9100 |
| rs147612042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84711704 | ACTAGAGTTTTAGGC[A/G]TGAGGAAGGGCTAGC | 9100 |
| rs147667172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84703481 | TCTTGGATTCCCCCT[C/G]TAGCATATGGCTGAA | 9100 |
| rs147686690 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84725036 | AAACTTTATTGAGAT[A/G]TAATTCACATGCTGT | 9100 |
| rs147714910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84753067 | GATCTCTCAGGCGCA[A/G]GTGGTCTTCCTGCCC | 9100 |
| rs147715804 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | USP10 | GRCh38.p7 | 16:84722505 | GCCATGCCGTTTTCT[A/G]TCTGCACCAGCAGTG | 9100 |
| rs147731345 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84748650 | TCCACAAAGGAAAAC[A/C]TCCCATCTTAGGGAG | 9100 |
| rs147820777 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84765717 | CTGTTGTGAACTGAT[G/T]GGAAGCAGGTGAGGT | 9100 |
| rs147820791 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | USP10 | GRCh38.p7 | 16:84734820 | GAGGCACTGAATTTT[G/T]TATATGTGTGAGGTG | 9100 |
| rs147836854 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | USP10 | GRCh38.p7 | 16:84763806 | CTGTTGCGATTGGTT[A/G]CCGTGGATCCAGTGA | 9100 |
| rs147887677 | in-del | -/TGT | 0.0283406 | 0.115616 | intron-variant | USP10 | GRCh38.p7 | 16:84766051 | GTGACACTCTTAGTC[-/TGT]TGTTGTCCCAAATGC | 9100 |
| rs147898030 | in-del | -/AAAAAAAC | 0.0156022 | 0.0869348 | intron-variant | USP10 | GRCh38.p7 | 16:84727456 | TTCAGTGTTAGCTTT[-/AAAAAAAC]AAACAAACAAACAAA | 9100 |
| rs147910446 | snp | A/T | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84703549 | GCTGGATTAGTGTTA[A/T]TTCTTAAAAGAGATA | 9100 |
| rs147925965 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84746274 | CTGCATAATTCACAG[A/G]TTGTTTTTAAAAAGT | 9100 |
| rs147926276 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84776446 | CGATCACAATTCCTC[C/G]TCAACTTGCTGGGCC | 9100 |
| rs147927039 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | USP10 | GRCh38.p7 | 16:84700617 | TTGATTGATGATGCG[A/G]GGGTTGCCGATTTTC | 9100 |
| rs147942885 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84774760 | AGGCGTGAGCCACCG[C/T]GCCTGGCCTGTAATT | 9100 |
| rs147995577 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84771289 | TTAAAACATCTAATT[A/G]GCCTGGAATCCCAGC | 9100 |
| rs148044417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84758963 | ACCTTGCTTATAAAC[A/G]GGATTATTCCTGACC | 9100 |
| rs148082646 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84710036 | GCACTTTGGGAGACC[A/G]AAGTAGACGGATCAC | 9100 |
| rs148099491 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84735891 | GAGTTGTTTTCCCCA[A/G]TCTTCAGGAATCTGA | 9100 |
| rs148153933 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84768065 | AGTATATTTTTGGCT[A/T]TTCTCTGTGGTCTTT | 9100 |
| rs148158720 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84701178 | GTCAATCTGACTACA[A/C]CTCTTTTGAAACATG | 9100 |
| rs148187112 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | USP10 | GRCh38.p7 | 16:84749592 | AAAAAAAAAAAATTA[C/T]ACACACACAAAATGC | 9100 |
| rs148241230 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84755053 | GTTCTTGATGGCTGT[C/G]CAATGCTTTCCTTTT | 9100 |
| rs148257588 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779842 | CTTCTCTAATGCTGC[A/G]TCCCTAATTGTACAC | 9100 |
| rs148311442 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84712719 | CTGCATTTAGAATGC[A/G]TGAGTGACCCCTAAG | 9100 |
| rs148362474 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84715877 | GGCTAGTTTCCCCCA[C/T]GATGGCGGAATGGCC | 9100 |
| rs148366702 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84742110 | GTAGGTACATAATAG[A/G/T]TGTATATATGTATGG | 9100 |
| rs148368570 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | USP10 | GRCh38.p7 | 16:84722756 | GTAGAGATGGAGTTT[C/T]ACCATGTTGGCCAGT | 9100 |
| rs148380376 | in-del | -/A/CTGCCAGGCCCGGGTGA | | | intron-variant | USP10 | GRCh38.p7 | 16:84735221 | GTGTGTGTGTGTGTG[-/A/CTGCCAGGCCCGGGTGA]TGTGTGTGTGTGTGT | 9100 |
| rs148419293 | snp | A/G | 0.0930568 | 0.194599 | intron-variant | USP10 | GRCh38.p7 | 16:84720925 | TTGGGAAGGAGTCTC[A/G]CTCTTTTGCCCAGGC | 9100 |
| rs148463489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84765861 | ATTCACAAAGTCCTT[C/T]GGAAAGGTTTTTCTT | 9100 |
| rs148471122 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84724769 | TCTCGTAGTCTCGCA[C/T]AGTTGAGTGTGGATT | 9100 |
| rs148487760 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | USP10 | GRCh38.p7 | 16:84752035 | ATGTCTTAAAATTTG[A/C]AAAAAGGCTATTAAG | 9100 |
| rs148489454 | in-del | -/C | 0.00557542 | 0.0525036 | intron-variant | USP10 | GRCh38.p7 | 16:84761514 | GCCTAAAGGAAACTT[-/C]CAGACTCCTCTCCCA | 9100 |
| rs148523335 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84705830 | ATTCAAGCGATTCTC[C/G]TGCCTCAGTCTCTCA | 9100 |
| rs148540192 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84730553 | GAACCGTTTCTGAGC[A/G]TTCCAGCTCATGACT | 9100 |
| rs148589496 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84733782 | CCAGAAGTAACTACT[C/G]TGCTGAAATTGGGAA | 9100 |
| rs148680656 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84703170 | ACTCAGCATTTTAGC[A/G]AAGACAAATAAATGA | 9100 |
| rs148687496 | in-del | -/TCTT | 0.093417 | 0.194889 | intron-variant | USP10 | GRCh38.p7 | 16:84705593 | CTCCGTCCCTTTCCC[-/TCTT]TCTTTCTTCCTGATC | 9100 |
| rs148695375 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | USP10 | GRCh38.p7 | 16:84775843 | CATCATCTTCCCTTT[C/G]CTTTCTGCCTTCCCT | 9100 |
| rs148741686 | in-del | -/TTT | | | intron-variant | USP10 | GRCh38.p7 | 16:84714936 | TATTATTATTATTAT[-/TTT]TTTTTTTTTTTGAGA | 9100 |
| rs148747194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84756979 | GGCTCAACCTCTTGA[A/G]TCAGGTGGACCCAGG | 9100 |
| rs148749664 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84708429 | TCACTCCAGCCTGGA[C/T]GAAAGAGTGAAACTC | 9100 |
| rs148802368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84711282 | ACACATGTGTTCCCC[A/G]GAACCTTAAGAGCTG | 9100 |
| rs148854126 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84709570 | TAGACTCACGGGGTC[A/G]CAGTGGCCATAAGGA | 9100 |
| rs148921831 | snp | C/T | 0.000418715 | 0.0144631 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764119 | GCCCCAAAAACCACT[C/T]GGTCAATGAAGAAGA | 9100 |
| rs148954467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84721956 | CACCTTGGCCTCCCA[A/G]AGTGCTGGAATTACA | 9100 |
| rs149010158 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84754189 | TGTGGAGAATCTTGA[A/G]TGCCTTCTGTCGGTC | 9100 |
| rs149058863 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | USP10 | GRCh38.p7 | 16:84707282 | ATGAAATGTGCATTT[A/G]GAAACTTTAATGTTA | 9100 |
| rs149060913 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779759 | TGCTTCTGTGTACAC[A/G]TAATGAAAAATGGGC | 9100 |
| rs149061202 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84731254 | AGAGTGCTGGGATTA[C/T]AGGTGTGAGCCACCG | 9100 |
| rs149147092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719172 | AAAAGCACTAAAAGA[A/G]TTCCCATTTTAAAGA | 9100 |
| rs149164354 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP10 | GRCh38.p7 | 16:84745881 | GTAACTTTATGTTAA[A/G]TGAAAGATCCATGTC | 9100 |
| rs149205838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84704266 | CGTGGTTGCTGAGGA[C/T]ACTTATTACTGGTAC | 9100 |
| rs149215350 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84749179 | TTTTGTTGTTTTATT[C/T]TCCTACTTAGGGATT | 9100 |
| rs149238187 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | USP10 | GRCh38.p7 | 16:84720644 | TGGAGTGCAGTGGTG[C/T]GATCTTGCCTTACTG | 9100 |
| rs149320165 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | USP10 | GRCh38.p7 | 16:84750895 | GAATTGTTAGTCAAA[A/T]CCTGTTTATATGATT | 9100 |
| rs149322051 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | USP10 | GRCh38.p7 | 16:84705313 | CTTGTCTCACTGCAA[C/G]TTCTGCCTCCCGGGT | 9100 |
| rs149336581 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84777553 | GTGTCCCTGGCTCTC[C/T]GAAGTACGGGCCCCA | 9100 |
| rs149372403 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | USP10 | GRCh38.p7 | 16:84730151 | CGTCCACTCAGTGCT[A/G]CTGTCCCAAAGGTGA | 9100 |
| rs149390088 | snp | A/G | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84760074 | CCATTCTCAACATTC[A/G]GCCAGGTGGGAGGTG | 9100 |
| rs149442468 | in-del | -/GTGTGTGTGTGTGTGTGTGTGTGT | | | intron-variant | USP10 | GRCh38.p7 | 16:84735197 | TGCCAGGCCCGGGTG[-/GTGTGTGTGTGTGTGTGTGTGTGT]GTGTGTGTGTGTGTG | 9100 |
| rs149464286 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698009 | GTGAGCCACCGCACC[A/G]AGCCAGAGAGACAAC | 9100 |
| rs149477834 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84773577 | CCAGGCCTGCACACA[A/G]GAGCTGTGCTTTCTG | 9100 |
| rs149482320 | in-del | -/GGCGAGGGCGTGTCACTTGGACCTGTGGGTGTGTGAGT | | | intron-variant | USP10 | GRCh38.p7 | 16:84735982 | GTGGGTGTGTGAGTG[lengthTooLong]GCGAGGGCGTGTCAC | 9100 |
| rs149531196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84775549 | GCTTGTGGCACCTGT[A/G]GGTGACAGTGCTGTG | 9100 |
| rs149589565 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84732857 | AAAATCACATTCTGA[A/G]TTCCGTGAAATCAGG | 9100 |
| rs149608035 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84741918 | CCTGTAGTATCTGGA[A/G]TGTTGTAAGCCCTCA | 9100 |
| rs149705636 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | USP10 | GRCh38.p7 | 16:84716994 | AGTAGAGCTTCGGGA[C/T]TACATGAGATAGAGC | 9100 |
| rs149708293 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP10 | GRCh38.p7 | 16:84743063 | TTCAATCTGGGGAGC[C/T]TTGACGGCCCCAGAA | 9100 |
| rs149762757 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | USP10 | GRCh38.p7 | 16:84721637 | GGTTCAAGCCATCCT[C/T]CTGCCTCAGCCCTCC | 9100 |
| rs149830196 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84753471 | ATTGAGCTGGCCGTC[A/G]TGCCGGGAGTGGTCT | 9100 |
| rs149852062 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84713564 | GCAGGGGTTTTTGTT[G/T]GCTTTGTTCACTGCT | 9100 |
| rs149860427 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84778792 | CTGCTTTGGAGAGGG[G/T]TTTTACACATAGGAT | 9100 |
| rs149862235 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP10 | GRCh38.p7 | 16:84763412 | ATACACACACTGTGT[A/G]TATATATATATGTCT | 9100 |
| rs149913717 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84761726 | GTTCAGCAGAAAGCA[C/T]ATTGCTTGCGCAAAC | 9100 |
| rs149920446 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84769157 | TCCTGCAAAGCGATA[G/T]TTGAATAATGGGCAG | 9100 |
| rs149973363 | snp | A/C | 0.00221651 | 0.0332166 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745563 | CGGTGGCCTATGTGG[A/C]AACTAAGTATTCCCC | 9100 |
| rs149975143 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699884 | TCCAGGCGGGGCAGG[A/G]GATGTCCGCGGCCCG | 9100 |
| rs149989842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84774620 | AGACTACAGCCGCGT[A/G]CCACCACGCCCGGGT | 9100 |
| rs150007084 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | USP10 | GRCh38.p7 | 16:84708307 | ATACAAAAATTAGCC[A/G]AGTGTGGTGGCGGGC | 9100 |
| rs150039658 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84776764 | AACCTGCCTCGCCCC[A/G]GGACCTGGGCCTGGG | 9100 |
| rs150055595 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84727667 | ACTCATACGGATACA[C/G]ATACAGACACACAGA | 9100 |
| rs150073218 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84736699 | GAGTCAATAAGCCCC[C/T]GATGACATAGTGTTG | 9100 |
| rs150077055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84701540 | TAACTAGCTTATTAG[A/G]ATTGGTATGAACAAG | 9100 |
| rs150086680 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | USP10 | GRCh38.p7 | 16:84747407 | GGTGATAGCAAGCAA[C/T]GTATATATATTTTTA | 9100 |
| rs150090285 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84775235 | TTGCAGGTGAGTAAA[G/T]TTGTACGACATTACT | 9100 |
| rs150106720 | in-del | -/CCG | | | intron-variant | USP10 | GRCh38.p7 | 16:84778460 | GGCTATTGAGGTTTT[-/CCG]TTTTTTCACTGTTAT | 9100 |
| rs150143754 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84777458 | CAGGGGACATGCTGC[C/T]GTCATGGGTGCTTCC | 9100 |
| rs150145160 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84729544 | ATATGGGGAATACTC[A/G]TTGTATGGGAGATGG | 9100 |
| rs150161106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84712206 | TATACTTTGATTCTG[C/T]AGATGCCCTGTCCTT | 9100 |
| rs150177753 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | USP10 | GRCh38.p7 | 16:84738490 | GAGACACACATGGCC[A/G]CTGTGTCCACTGCCC | 9100 |
| rs150233675 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | USP10 | GRCh38.p7 | 16:84743841 | AGAGATATTTAAAAG[C/T]TCACAATTCTAACTT | 9100 |
| rs150284160 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84724034 | TCTTGAACTTCTACT[A/T]GGGCTATCCCAGATA | 9100 |
| rs150302570 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | USP10 | GRCh38.p7 | 16:84731139 | TGCATGCCACCATGC[C/G]CGGCTAATTTTTTGT | 9100 |
| rs150352264 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84755949 | TGTTGTATTCCTCCT[C/T]TAGTTGGATAGCACT | 9100 |
| rs150386092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84763951 | CGTTGCTCCTGTTGC[A/G]ATTGGTTGCCGTGGC | 9100 |
| rs150387520 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84714581 | AACTTAATCTTCAGC[A/T]TTGTTTTTTAAGGAC | 9100 |
| rs150446160 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84703807 | GATGGCCTGAGCAGC[C/T]GCGCCGTACCAGGAC | 9100 |
| rs150528668 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84742628 | TCCTAATGTATTGAT[C/T]GGGTTGTTGAAGCCA | 9100 |
| rs150550646 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84705051 | CCGTTGGGCTTGTGT[C/G]TACAGCCTTATCGGT | 9100 |
| rs150557914 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84771707 | AACCCCTTCTTTACT[A/G]AAAATACAAAATTAG | 9100 |
| rs150616871 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84759767 | TTCACTAGCTGTTAC[A/C/G]GCATTGGTTACCTAA | 9100 |
| rs150670341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84713463 | TAATACCCTACATAC[C/T]CGCTATCCTGACGTG | 9100 |
| rs150700912 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | USP10 | GRCh38.p7 | 16:84739742 | TTTCTGTCTGCCAAA[C/G]AAGGAATGTGACTTC | 9100 |
| rs150753219 | snp | C/T | 0.0452528 | 0.143452 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718584 | AACATGGTAAAACCC[C/T]GTCCCTACTGAAAAT | 9100 |
| rs150770906 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP10 | GRCh38.p7 | 16:84726324 | GTGCAAGTGAACATT[A/G]GACATCTTTTCTCCT | 9100 |
| rs150822395 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | USP10 | GRCh38.p7 | 16:84724906 | CTGAAGTTGAAAGCA[C/T]ACAATGATTGTTCAG | 9100 |
| rs150829174 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP10 | GRCh38.p7 | 16:84732600 | TACAGGTACACGCCA[C/T]CACGCCTGGCTAATT | 9100 |
| rs150855971 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84747751 | TTTGTATTTTTAGTA[A/G]AAATGGGGTTTCACC | 9100 |
| rs150896555 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84764660 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 9100 |
| rs150913710 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84716063 | CCAAGCAGGGCTCCC[A/G]TCTGGCCTGGGGGTG | 9100 |
| rs150929644 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84708914 | AGAGCTGAAGAGAGA[A/T]TTCCTGTGCTTTAGA | 9100 |
| rs150931540 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP10 | GRCh38.p7 | 16:84734185 | CTCTTTAGTTTCACT[A/G]GAGACTGCTCGTTTG | 9100 |
| rs151001048 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84766196 | CTGCGCTGACGCCCT[C/G]AGAAGCTGGTTTCCC | 9100 |
| rs151017844 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699335 | ACCAACGACCCCCAA[C/G]GCTGGTTTGCCCGTG | 9100 |
| rs151054739 | snp | A/T | 0.00915221 | 0.067025 | intron-variant | USP10 | GRCh38.p7 | 16:84743632 | TAAGGCATGTGTCCT[A/T]CCCTTAACTTCAAAA | 9100 |
| rs151065682 | in-del | -/AA | 0.0138799 | 0.0821421 | intron-variant | USP10 | GRCh38.p7 | 16:84773184 | TTTGAAAGCAATTTT[-/AA]AGAGCCCCAGGTTAA | 9100 |
| rs151084551 | snp | A/G | 0.0012578 | 0.0250463 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84772570 | AAGAGTGACTCTGGA[A/G]AAACTCCCTCCTGTC | 9100 |
| rs151088652 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84705890 | ACGCCCAGCTAATTT[G/T]TTTGTATTTTTAGTA | 9100 |
| rs151101492 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84778618 | GTGTCTGTGTGAGGC[A/G]TGGGACATTTTAAAT | 9100 |
| rs151122134 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84774911 | AGGGGCCTCCCACAG[A/G]AGCATCACAGCCTCG | 9100 |
| rs151145150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84711449 | GAAGCCTGGTTGTCA[A/G]CATCTCTGAGGATGT | 9100 |
| rs151155196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84761618 | AAGGTCATTACAGAC[C/T]CCGTGTCCAGAGTTT | 9100 |
| rs151196747 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84714077 | TCAGTTGAGAGACAG[A/C]TCTGTGGTGGCCACA | 9100 |
| rs151212700 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | USP10 | GRCh38.p7 | 16:84740503 | TTGCTGTAAACTGTA[A/G]TGTATTTAATTGCTG | 9100 |
| rs151262860 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84769875 | GTTGAGGCGCAGGTA[A/G]TTGTTAGCCTGTTGT | 9100 |
| rs151266780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719413 | TCCAACTGTAAGTCA[A/G]AATCACACAGGAAGT | 9100 |
| rs151301843 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | USP10 | GRCh38.p7 | 16:84757068 | GGTAACTATCTCTGA[C/T]AGTAGGGTTATGATA | 9100 |
| rs180680851 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84735051 | TTTTCTTTTTTTCGA[C/G]ACAGGGTCTCACTCT | 9100 |
| rs180690308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84721909 | CACCGTGTTGCCTAG[A/G]CTGATCTTGAACTCC | 9100 |
| rs180703355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84746377 | CTAAGATGGATATGT[A/G]TTCCGAGATGTGCGT | 9100 |
| rs180711357 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84757149 | GGTGCTATCTCTGCT[G/T]GGTGTCATCACATGC | 9100 |
| rs180717897 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84771831 | GCAGATCGTACCACT[A/G]TACTCCAGCCTGGGC | 9100 |
| rs180736410 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698304 | AGTTTACAGGCATTA[A/T]GGCCTTCACTCCTCA | 9100 |
| rs180833857 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84764745 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG | 9100 |
| rs180849309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84778477 | GTTTTTTCACTGTTA[C/T]AAATGACATCATAAT | 9100 |
| rs180856362 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751858 | AATATGACCCCTAAG[G/T]CCTAATTTTAGGAAA | 9100 |
| rs180866881 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699355 | GTTTGCCCGTGCACA[A/C]GCACGCACGTGTGCA | 9100 |
| rs180986276 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84754485 | CACGTCCCAAGGGCC[C/G]GTACGTATGTTCTGC | 9100 |
| rs180998615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84768428 | AAGAACACAAAATTA[A/G]GAATGAGGGGAAATG | 9100 |
| rs181007321 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84711882 | GTGCCACCATGGCTG[C/G]CTAATTTTTGTATTT | 9100 |
| rs181027137 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84707182 | TTGCCAGACTGGTTT[C/T]CTGGAAGAGACTGAT | 9100 |
| rs181070041 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84742716 | CCATGCGGTGCAAGG[A/C]ACATGGCGTCCATTG | 9100 |
| rs181077539 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84731968 | AAGATCATTTCTGAA[C/G]CATTTTGAGGCTCTG | 9100 |
| rs181209668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84724543 | TTTGTCTACTTTGTT[C/T]GCTTCTCAGGACCTC | 9100 |
| rs181241347 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84712464 | CACTCAGGTGTTTGT[A/C]TGTTGGATCGGTTAA | 9100 |
| rs181241585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84732181 | CCATTTATTCACATT[C/T]ACAATAATAATGAGT | 9100 |
| rs181244305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84760364 | TATTGATATTTGCCC[C/T]CTGTCTCCAGCGCTA | 9100 |
| rs181257473 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84749080 | AGTTTCAGGAGTCTC[G/T]TGAGATAGTAGAGCA | 9100 |
| rs181265280 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84774479 | TTTGTTTTGTTTTTT[G/T]TTTGTTTGTTTGTTT | 9100 |
| rs181269801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84743109 | GATGTATGGAACCAA[A/G]ATGAACAGCCAGCCC | 9100 |
| rs181346517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84768951 | TCAACTCAGTTGGGC[A/G]AGACGGATAGCATTC | 9100 |
| rs181440976 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84742523 | TCTCTACTGCATGTA[A/C]TGCAGTGAGCAGCCT | 9100 |
| rs181442251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84712810 | TGACTGACCCGCACG[C/T]CACATATAAGTTATT | 9100 |
| rs181444605 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84753420 | CCTTCCACCTCTATT[A/T]GCTCTTTATTTTCTA | 9100 |
| rs181454174 | snp | C/T | 0.0123036 | 0.0774623 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699954 | GCGGGCCGGCCTCCC[C/T]GCGCCCCGCGGCGCG | 9100 |
| rs181454421 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84731719 | TTGAGTTTTTTAATT[C/T]AGTGATTTAAAATTA | 9100 |
| rs181455560 | snp | C/G | 0.0456336 | 0.143994 | intron-variant | USP10 | GRCh38.p7 | 16:84738101 | AGCTCTCTGCCTTGT[C/G]AAGTGGATGGGTGAA | 9100 |
| rs181475747 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84768002 | AGCATGCTGCCTTCA[A/C]GCATCTGTTTAACAA | 9100 |
| rs181478621 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780421 | AGAAGGGGTTTTAAC[A/G]TGGTCTGAGCCTTTC | 9100 |
| rs181487748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84754598 | TTTTAATACTGTGCA[A/G]GAAAAACTGAAACTG | 9100 |
| rs181501535 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84761127 | ACATGGTGTTAGGGA[C/T]GCAGAAATGGAATGA | 9100 |
| rs181503368 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | USP10 | GRCh38.p7 | 16:84738824 | TTGGTGTGCTGAGAT[C/G]TCATTGGAGAACTCA | 9100 |
| rs181509565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718332 | AATCATGGCTCACTG[C/T]AGCCTCAAAGTTATT | 9100 |
| rs181609634 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84725329 | GCTTTAACTTAGTAT[A/C]ATGTTTTCAAAGTCA | 9100 |
| rs181622401 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84749370 | TTATAATAGAGTTTG[A/G]CTTGCATTAGTATCT | 9100 |
| rs181637134 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84746882 | CATTTAGCTTAAAAC[A/C]CACACTACAGCTATA | 9100 |
| rs181651322 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84772251 | AGACGGGATTTCACC[A/G]TGTTGGCCAGGCTGG | 9100 |
| rs181695088 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84706791 | GGGATCTGCCCACCT[C/T]GGCCTCCCAGAGTGC | 9100 |
| rs181725482 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84728310 | AAATATATTGAATAA[A/G]TTGAATAAATAATTG | 9100 |
| rs181729927 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84703591 | GAATCTCAAGTAATG[A/G]GCAGCTGAAGTAAAT | 9100 |
| rs181787718 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | USP10 | GRCh38.p7 | 16:84774662 | TTTTTAATAGAGACG[G/T]GGTTTCACTGTATTA | 9100 |
| rs181824040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84777353 | CTGCAGATTCTACTG[A/G]TGGTCGCTTTGAAGC | 9100 |
| rs181877813 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84716022 | TCGTCCCTCAACCAG[A/G]GCACTGTGGCGAGGA | 9100 |
| rs181894634 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84751421 | ATTTTGCACTTCCTC[C/T]TCAAACTCTGAAGTA | 9100 |
| rs181962640 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741065 | CCCTTACTGGCCTCC[A/T]GGAAACTGATGCCAA | 9100 |
| rs181967980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751686 | TTCTTCCAAATTGAT[A/G]GTAATGAGGAAAAGA | 9100 |
| rs181972120 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84728541 | GACGGGGTTTAGCCA[C/G]GATGGTCTCAATCTC | 9100 |
| rs181991840 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84764556 | AGCTAATTGGCCATA[C/T]GCGGTGGTTCATGCC | 9100 |
| rs181995291 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84778241 | CGTGGTTAGCAGTCC[C/T]AGGGTCCCTCCTGCC | 9100 |
| rs182033297 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84721181 | ACAGGTGTGAGCCAC[A/C]ATGCCCGGCAATGAT | 9100 |
| rs182039902 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84704430 | TGCTGGCCTTGGGCC[A/G]TTGGATTACTGTCAT | 9100 |
| rs182092186 | snp | A/G | 0.000124892 | 0.00790129 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764093 | CTTTTCAGAACTTAC[A/G]ATTTCCAACGGCCCC | 9100 |
| rs182120578 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84711361 | ACAGCATGGGATCAG[C/T]ACACTCCCCCACAGC | 9100 |
| rs182125350 | snp | A/C | 0.00318978 | 0.0398085 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698856 | CCGCCTCGGCCTCCC[A/C]ATGTGTGGGATTCCG | 9100 |
| rs182136127 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698527 | ATTTGGTTATGTTTT[C/G]TAGCTCTTCTATTTT | 9100 |
| rs182168784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84722310 | TATTCCTTTGTGGAT[A/G]TCCCACAGTTTGCTT | 9100 |
| rs182195514 | snp | C/T | 0.0005137 | 0.0160183 | intron-variant | USP10 | GRCh38.p7 | 16:84740395 | TCTCTCCTTATTTCC[C/T]TGAAGGGAATTTGGC | 9100 |
| rs182254406 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84747982 | ACGGTGAAACCCCGT[C/G]TCTACTAAAAAAAAC | 9100 |
| rs182274601 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84736821 | TGAGAGGGAGTCTCG[C/T]TCTCTCGCCCAGGCT | 9100 |
| rs182279230 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84773500 | GGCTGGCTTCTAGCC[G/T]GCTCCCTGTCTACCC | 9100 |
| rs182285739 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84758318 | AAGATATCTTTCTAT[C/G]TAGTGTCTGAGGCGC | 9100 |
| rs182286528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84709181 | GAAGACAGCTTGCTA[A/G]TCAGATAATCACAGT | 9100 |
| rs182315409 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84734501 | CTTTTTCTTACTGAT[C/T]TTAGGATTAATCTTT | 9100 |
| rs182375429 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84741294 | AGAGCAGATCTAACA[A/G]TAGCTTAGGACAAGT | 9100 |
| rs182393504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84716601 | AGGAGGTGATGCCTG[C/T]GTTGAGCTTTGAAGG | 9100 |
| rs182395568 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84749763 | ACTAAAAGAATCACG[G/T]ATAAGGGATTTTGAA | 9100 |
| rs182403471 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84725786 | GGGAAGAATTTTAGA[A/C]GTTGTCTGGTCCAAC | 9100 |
| rs182406396 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84739217 | GCACCCACCACCATG[C/G]CCGGCTAATTTTTTG | 9100 |
| rs182410246 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84774899 | CACCTGTTTTTAAGG[A/G]GCCTCCCACAGGAGC | 9100 |
| rs182422872 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84761550 | GCCACAAGGCTACGC[A/G]TAACTACTCCAGCAC | 9100 |
| rs182457199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84756614 | CAAAGGTTTCTATGT[C/T]AGAAAGATAGCAGGC | 9100 |
| rs182469876 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84707841 | CCCAGCACTTTGGGA[A/G]GCTGAGGCAGGCGAA | 9100 |
| rs182477247 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84713128 | CGGTTGGTTTGCCAC[A/G]GTTAGTTTATCTTTC | 9100 |
| rs182486183 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84700838 | ATCCCGTGGTGGAAA[C/G]AAAGAGCTCTTTTTG | 9100 |
| rs182555897 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84758652 | GAGTAGAGCATGTGA[A/C]ATGATTTGAATGTTC | 9100 |
| rs182614140 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84704624 | GGTAGCCCTTGGGGT[A/G]TGTGTATAGTATTTG | 9100 |
| rs182657433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84729316 | TTTTTCAAAATGTGC[A/G]TTGCAATTCTAAGAA | 9100 |
| rs182683664 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84708496 | TCAGATTCTTGTCCA[C/T]CCATTGCCTTTGCAC | 9100 |
| rs182696362 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84762477 | AGGCAGGTCACCTGA[A/G]GTCAGGAGTTTGAGA | 9100 |
| rs182696393 | snp | A/G | 0.000216983 | 0.0104137 | intron-variant | USP10 | GRCh38.p7 | 16:84775273 | TAAAACACTGATGAA[A/G]GGGTTTACAGCTGGG | 9100 |
| rs182700876 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84755098 | CCTCGTCATAAAGCG[G/T]GTTTTTGAGTCTGTT | 9100 |
| rs182712405 | snp | C/T | 0.000532871 | 0.0163142 | intron-variant | USP10 | GRCh38.p7 | 16:84733425 | CAGTGACTCTCTTAT[C/T]TTTTTTCAGTATATT | 9100 |
| rs182732417 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84701827 | TGGCGGAACGTAAAT[A/G]TTAGCAACACTTTGG | 9100 |
| rs182742097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84732793 | GAATATGAACTGGTA[A/G]GCACTTGCCAGACTC | 9100 |
| rs182844751 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | USP10 | GRCh38.p7 | 16:84754664 | TGGAAGCTGGTATCG[A/G]TTTAAGGGAATGGCT | 9100 |
| rs182854841 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84769393 | GCCTAATCTTCTACC[A/G]TATTTGCAGACTTGC | 9100 |
| rs182860514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84743734 | AACTTAACCTGATTT[C/T]AGAGGTGTAAACTAT | 9100 |
| rs182863339 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84727252 | ATCAGTGGCATTTCC[C/G]TCTTCACTAGGTTGT | 9100 |
| rs182864825 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84713937 | TGGAGAGTTGTCGGG[G/T]CTGCAGCACTGGGGG | 9100 |
| rs182950746 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719951 | TTATTTTCAACAGAT[A/G]GTAATTTTGCAGCTT | 9100 |
| rs182976227 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84729986 | ATTATGTCTGTGCAA[A/C]ATGGGTGTATTTGAA | 9100 |
| rs182976523 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741426 | TGGGACTTCCTCTGT[C/G]ACTGTGTGCTTTGCA | 9100 |
| rs182983187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84716662 | AGAGGGAGCTGCCTG[C/T]ACGAAGGCTGATCAG | 9100 |
| rs183000028 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84744327 | AGATTCCACTGGGGG[A/G]TATTTTTAAAATTGG | 9100 |
| rs183039808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84704941 | TGGGCTCACATGAGA[A/G]TTGTTAGGAGAATGT | 9100 |
| rs183062607 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84701260 | ACTTTTTAAAAAATT[A/C]GATCTTACGACAAGC | 9100 |
| rs183092176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84749850 | TTGGACCTTCTTGGT[A/G]GCAAGGCCATCTCCT | 9100 |
| rs183241254 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84766469 | CAGCAGCGAGGGAAG[G/T]CTGTGCCCTTTGCTC | 9100 |
| rs183252647 | snp | A/C | | | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719602 | AGGTGAGTACCACCG[A/C]GGATTGGTTACCTGC | 9100 |
| rs183262385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741760 | GCAGCCTTTCTGGGT[A/G]TCTTGTGTTTCCATG | 9100 |
| rs183264363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84752123 | TTTTCATGTGAGTTA[C/T]TACAAAAGTGAACTA | 9100 |
| rs183272912 | snp | A/G/T | 0.000593637 | 0.0172186 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779094 | GTAAACCCTGTGTGC[A/G/T]CTGTGTGTGCGCCCA | 9100 |
| rs183318960 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84713541 | GCCCCAATGTAAGCT[C/T]CGTGAGGGCAGGGGT | 9100 |
| rs183344062 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84739281 | TTGTTTTGTTTTGTT[C/T]TGGTTTTTGAGACAA | 9100 |
| rs183358077 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84730531 | AATAGGAGAAAAAAA[A/C]CTCAGTGAACCGTTT | 9100 |
| rs183387458 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | USP10 | GRCh38.p7 | 16:84739448 | AGCTGATTTTTTGTA[G/T]TTTTAGTAGAGATGG | 9100 |
| rs183410345 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84762749 | ACAGAAAGTATAAAT[A/G]ATAAAAATCCCCATT | 9100 |
| rs183450274 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84710824 | TCCCTGTGAGCAGGT[A/C]CCCAGGCCGTCTGAG | 9100 |
| rs183451759 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698645 | CTGTCACCCAGGCTG[G/T]AGTGCAGTGGCACGA | 9100 |
| rs183543410 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84760031 | GTAAATTCAGTCTTG[A/T]TGGGAAGATAGTGTC | 9100 |
| rs183560502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84774402 | AGGGAGTTCCCGCCT[C/T]GTAGCAGCTGGTAGA | 9100 |
| rs183564233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84748889 | AGTCCACGTAATTAT[C/T]TTTGTGTGGACATAT | 9100 |
| rs183570503 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84737500 | GAATGAAAGGTGCTG[C/T]GTGCCTGTGGAATAA | 9100 |
| rs183576608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84778741 | TGTTTGAGTTGAAAT[A/G]GCATTGGTTTGTGTG | 9100 |
| rs183583752 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751942 | TAAAAGTTTACGATG[C/G]TGGTATTGCCTTTGA | 9100 |
| rs183605150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84724348 | GGAATCTCCATGAAA[A/G]CACTTAATATACAGC | 9100 |
| rs183608694 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84738030 | GTGAGTGTTCACACC[A/C]CGTGGTTGAATGTTG | 9100 |
| rs183621566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84712278 | CTGTCCTGAGAGTAG[C/T]GGAAGGAAGACATGG | 9100 |
| rs183665182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84776000 | TGTGTCTTCCCTCCT[C/T]TGGTGTGGCCTTTGG | 9100 |
| rs183671894 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84750016 | GGATGTATCTAAACA[C/G/T]AAAAGCCCTGTCTTG | 9100 |
| rs183736503 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84727581 | CCTTTACCCAGATCC[A/G]CCTGTTGTTAAGATT | 9100 |
| rs183737843 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84709189 | CTTGCTAATCAGATA[A/T]TCACAGTTACGTACA | 9100 |
| rs183739475 | snp | C/T | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698008 | TGTGAGCCACCGCAC[C/T]GAGCCAGAGAGACAA | 9100 |
| rs183745523 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84714903 | GTTTGAAAAATATTT[A/T]AAAAGTTCTGATTAT | 9100 |
| rs183794964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84765869 | AGTCCTTCGGAAAGG[C/T]TTTTCTTTATTTACC | 9100 |
| rs183801750 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | USP10 | GRCh38.p7 | 16:84748479 | AGGCTAATTTTTGTA[A/T]TTTTAGTAGAGACCG | 9100 |
| rs183887474 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84773164 | AGGTCACGGGCTCGG[C/T]ACTTTTTGAAAGCAA | 9100 |
| rs183912345 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP10 | GRCh38.p7 | 16:84769954 | TGAAGGCTTCCAGAA[A/G]GAAGGCGGGCCAGGT | 9100 |
| rs183946513 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84722840 | GGATTACAGGTGTGA[A/G]CCACTGCGTCCGGCT | 9100 |
| rs183978393 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84705789 | CAGTGGTGCGATCTG[C/G]GTTCACTGCAGCCTC | 9100 |
| rs183990471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84747444 | TTTTATTCCTTATAC[A/G]AAATACATTATCTCA | 9100 |
| rs184024163 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84752804 | TGATGGTTATCGAAA[C/T]GAGTCAGGATGGAAG | 9100 |
| rs184031796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84731215 | CGATCTTCTGACCTC[A/G]TGATCCGCCCACCTC | 9100 |
| rs184040051 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84742239 | CTAAAGCTTGAGATA[C/G]CACTCCTTCACCCTG | 9100 |
| rs184126366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84757904 | ATTAACATTTGTCAA[C/T]TGTAAAGAACGTGCT | 9100 |
| rs184126718 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84777060 | TGGAAATGAGGTCAC[C/T]GGACTGGTTAGAATT | 9100 |
| rs184130841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84736122 | GGCGTGTCACTTCTA[C/T]AGCACAGTTTGGCCT | 9100 |
| rs184150441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84716791 | AAGATTCTACCTTTA[C/T]ATACACCTTACAATT | 9100 |
| rs184177272 | snp | A/G/T | 0.000517408 | 0.0160762 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745419 | AAAGCATAGACTTGG[A/G/T]CCCAACCAAACCCGA | 9100 |
| rs184187163 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84755557 | TTATCAATCTGTTGA[A/T]CCCAGGAGGTCGAGG | 9100 |
| rs184188762 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84734136 | TCCGGGACACAGACC[A/T]GGGAATGGAATTACT | 9100 |
| rs184228568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84766946 | CAGGAAGACTTCCCC[A/G]CCTTTCTTCCCCGGT | 9100 |
| rs184253984 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84708754 | ACTTGTAATAGAATG[C/T]AAAATCGGGGCTTCC | 9100 |
| rs184255408 | snp | A/G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84720565 | GATGCAGAATAAAAA[A/G/T]ATGATGCCCAATTTT | 9100 |
| rs184299285 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699511 | CGTGGCCCAGGCGCC[C/G]AGGCAGGACTTGGGG | 9100 |
| rs184301317 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717340 | CCTTTTAGAAATTTT[A/G]TGCAGATTAAATGAA | 9100 |
| rs184344995 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84741906 | TCTGTCACTGCGCCT[G/T]TAGTATCTGGAATGT | 9100 |
| rs184430456 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | USP10 | GRCh38.p7 | 16:84731004 | TTTTTTTTTTGACAC[A/G]GAATCTCTCTCTGTC | 9100 |
| rs184435207 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP10 | GRCh38.p7 | 16:84706397 | AATTGAGAGAAAAGT[A/G]CAAAGAGTTCCTATA | 9100 |
| rs184437542 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | USP10 | GRCh38.p7 | 16:84770839 | TTCGGAGGCTGAGGC[A/G]GGCGGATCACAAAGT | 9100 |
| rs184453640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84752466 | TCCTTGGTGGCCCGC[C/T]TTCCTCATTTTTATT | 9100 |
| rs184454439 | snp | A/G | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84756251 | CCGGTGCCTAGGCAG[A/G]GCTCAGCAGGGGTTT | 9100 |
| rs184517212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84745752 | AGACTGTGGTGTTAC[C/T]CATAACAATGGCAGA | 9100 |
| rs184567208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84763530 | CAGGTGCTAAAGCAT[C/T]TCCTGCGTAACCACA | 9100 |
| rs184582133 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84750500 | GTATGGCAGACACGT[G/T]GGGAGTGCCTTTGCT | 9100 |
| rs184584648 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84702976 | CCAGCCTGGGCGACA[A/G]AGCAAGACTCCCGTC | 9100 |
| rs184597186 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84776888 | CACAGTCTCCATTCA[C/T]TGCAACCTCTGCCTC | 9100 |
| rs184665812 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717974 | ATTTGTGATGGAAAG[A/G]GTATATAATTTATGG | 9100 |
| rs184672663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84706732 | TTTTTAGTAGAGACG[A/G]GGTTTCACGGTGTTA | 9100 |
| rs184727932 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84711711 | TTTTAGGCGTGAGGA[A/T]GGGCTAGCTTTTTTT | 9100 |
| rs184728320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84723833 | CTCCACAATCAAGAC[A/G]CCAGTTCTGTCATTC | 9100 |
| rs184777427 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699263 | ACCCAAGGGTGGACC[C/G]ACTGGCTGGAAAACA | 9100 |
| rs184781615 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84727930 | CATATAATGTCCTTT[A/C]TAGAATTTTCCCTTC | 9100 |
| rs184783087 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84767292 | CTGAGGCTAAATGAG[A/T]GATGGGCCGAACACA | 9100 |
| rs184791743 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP10 | GRCh38.p7 | 16:84703240 | GTCACTGAGGGGACC[A/G]GTTAAATTATTTGGG | 9100 |
| rs184796051 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751287 | CTAATGCCACATTTC[A/T]CAGAACATATCCCCA | 9100 |
| rs184798237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84770498 | CCTCAGTTGGCTGGG[C/T]GAGGTGGCTCACACC | 9100 |
| rs184889868 | snp | C/T | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84715488 | AAGGAATAGGATCTC[C/T]GCCTCCCAAAGTGCT | 9100 |
| rs184920676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84763936 | CCGTGGATCCAGTGA[C/T]GTTGCTCCTGTTGCG | 9100 |
| rs184924742 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84739841 | ATAGTGCGCTTTCCT[C/G]TGCTCTCCGACCATG | 9100 |
| rs184943699 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84742661 | CGTGCAGGCCGTCCT[A/G]CACTTCGTCTGCCTG | 9100 |
| rs185057652 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84707304 | TTAATGTTACTAATT[A/G]CAAAATTTGTTACTA | 9100 |
| rs185077292 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84753558 | TTACCTGTTCCAGGT[A/G]CGGAGTGATCTGCCG | 9100 |
| rs185085167 | snp | A/G | 0.00023673 | 0.010877 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84768250 | GCAGCCATTTTTCAC[A/G]TTGCAGTTGGATATC | 9100 |
| rs185110322 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84764450 | GTGGCTTATTCTCTC[C/T]CTGCTGGCGCATGTC | 9100 |
| rs185162940 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | USP10 | GRCh38.p7 | 16:84720813 | GGTCTCGATCTCCTG[A/C]CCTCATGATCTGCCC | 9100 |
| rs185210954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84777891 | TGCCCTGTCATTCCC[C/T]GCGGAATGCTGCCGG | 9100 |
| rs185245426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84709000 | TAGGGTGGTAATTCC[C/T]GTAACACAAGTGTGA | 9100 |
| rs185247913 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84749800 | TACATTAAACTCTTG[A/G]TTACTCTTAAACTAT | 9100 |
| rs185253684 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84725851 | ATCATGCCAAACAGT[C/G]TATTGCTCTTTTCAT | 9100 |
| rs185261517 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84739219 | ACCCACCACCATGCC[C/T]GGCTAATTTTTTGTA | 9100 |
| rs185274095 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84769021 | TGCCAGCTTATAGCT[A/G]TTTTGTACTCTGCAG | 9100 |
| rs185276435 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84774544 | GGCGCGATCTCGGCT[C/T]GCTGCAACCTCTGCC | 9100 |
| rs185279959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84734481 | TTTTAAATCAAGTAG[C/T]TTGTCTTTTTCTTAC | 9100 |
| rs185282520 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84743360 | AAGCATACGAAGATT[A/C]AGGAGGCCTCGGGAG | 9100 |
| rs185290680 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84754626 | CTGCTTTTTAACCTG[C/G]CTGCGCCTCAAAATA | 9100 |
| rs185362415 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84707866 | GGCGAATCACTCAAG[C/G]TCAGGAGTTTGGGAC | 9100 |
| rs185364238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719579 | ATGGTTTATGCTGCT[C/T]CCCTGCTAGGTGAGT | 9100 |
| rs185379917 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84761771 | CCCGTATCAGTTATT[A/G]GACCGATGGGAACCT | 9100 |
| rs185385962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84774957 | TCTTTAGTGAGCTGG[C/T]TGCACATTTTGTGTC | 9100 |
| rs185401579 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698991 | CATCTCCTCTGCTCA[G/T]TGTACGGTCTAGCAA | 9100 |
| rs185413721 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84734598 | GGGTTGGGTTTTTTT[G/T]TTGTTGTTGTTGGAT | 9100 |
| rs185428380 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84723741 | TTATGGAGGTATAAC[A/G]TATGTGCGGTGAATT | 9100 |
| rs185473006 | snp | C/G | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698313 | GCATTATGGCCTTCA[C/G]TCCTCAACTCTTCAG | 9100 |
| rs185510314 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84735057 | TTTTTTCGAGACAGG[G/T]TCTCACTCTGCCCAG | 9100 |
| rs185516943 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84722131 | TCCAGGCAGCTAGTG[C/G]TCTGCTTCTGTCACT | 9100 |
| rs185517293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84709743 | CGTCTCTTGTAGAAC[A/G]GTGACATTTGAGCTG | 9100 |
| rs185547740 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84745922 | TCTTTTCTGTTGACA[A/G]GTTACATTTCCATTT | 9100 |
| rs185562292 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84721192 | CCACCATGCCCGGCA[A/G]TGATGCAGAATTTTT | 9100 |
| rs185582155 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84771551 | GTATCAGTTTTATCA[A/G]TACTATCAGAGTTAT | 9100 |
| rs185591783 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84748633 | TTCGTTTCTAAAATT[G/T]CTCCACAAAGGAAAA | 9100 |
| rs185596072 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP10 | GRCh38.p7 | 16:84773895 | TGATTTTATTTTTAT[A/G]TCTTTTCTTGCTTGC | 9100 |
| rs185602159 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84731751 | TAATTAATTTCCGCG[A/T]ACACTTTCATGATCT | 9100 |
| rs185619612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84757194 | GTTCGTAACTGATCC[A/G]TTATTCATTTATTTC | 9100 |
| rs185635109 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84771847 | TACTCCAGCCTGGGC[A/G]ACAGAGTGAGAACTC | 9100 |
| rs185637125 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84746581 | ATAGTACAGATATGG[C/T]ATAAAGGATGAAAAG | 9100 |
| rs185689904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84737966 | TCTGTGTATTTTTCC[C/T]GATTGCTGGGGTTTT | 9100 |
| rs185693909 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718641 | ACATGCCTGTAATAC[C/T]AGCTACTCGGAGGCT | 9100 |
| rs185734030 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | USP10 | GRCh38.p7 | 16:84759595 | AATTCTGTCTTTTTT[A/T]AAAAATAGACTGTTG | 9100 |
| rs185799880 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84757510 | GGATCTGCCAGTACA[A/G]TGTAGTTTAGAAAAG | 9100 |
| rs185866308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84742985 | CGTTCTAGTTTCTAA[C/T]GTGATTTCACAGCCT | 9100 |
| rs185868400 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718945 | TTACAGGCGCCCGCC[A/C]CCGCACCCAGCTAAT | 9100 |
| rs185880176 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84768608 | TTTATCTTGAGCTAC[A/C]TTTAATTTTCTGGCA | 9100 |
| rs185925682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84772396 | AGATCTCAGAGCTTC[C/T]GTGGGGCAGGAAAAG | 9100 |
| rs185984854 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | USP10 | GRCh38.p7 | 16:84713253 | AGAAATGGAGGGGAA[C/G]ACATTGTCTGTCCCC | 9100 |
| rs185986912 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84732020 | AATACATAATTTCTT[G/T]GTTGACTTTTGCAAG | 9100 |
| rs186015066 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84740632 | TTTCCTAACAGTTCT[G/T]AGTGCAACAGGTATG | 9100 |
| rs186027207 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84754519 | TGCAGAGGTTGTGCT[C/T]GTTCGCTTTTGTAGG | 9100 |
| rs186071421 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84715831 | TTTTCATTTCTTCAT[C/T]TTTTCATTCTGCCTG | 9100 |
| rs186218472 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84712596 | CATGAAGTTCAGGAC[A/C/T]ACAGCATGCAAGACC | 9100 |
| rs186235028 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84760376 | CCCTCTGTCTCCAGC[G/T]CTATAAGTAGATGTA | 9100 |
| rs186245460 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84738224 | ACAGAATACTGGGAA[G/T]TGTGAAGAGAACATT | 9100 |
| rs186294251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84764628 | CTGAGGTTAGAAGTT[C/T]GAGATCAACCTGATC | 9100 |
| rs186294314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84778363 | CATAAGCGTATTCCC[A/G]CATCACCATTCTTAA | 9100 |
| rs186338585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741200 | AAAGACTAACCAAAC[A/G]TTTTATCTCCAGTAA | 9100 |
| rs186343166 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84751732 | TGTTCTGGACAGTTA[A/G]AATGATGACAGAAAA | 9100 |
| rs186365835 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84724827 | TGGCGAACTTCCTGG[C/T]GTGCATTCACTAGTT | 9100 |
| rs186373767 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699614 | TCTAATGCGAACACT[C/T]CCGAGGCCCGGGCCC | 9100 |
| rs186380348 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | USP10 | GRCh38.p7 | 16:84704778 | CATCAGATGACTTGA[G/T]AACCCAGAAGCTCTA | 9100 |
| rs186413462 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84749088 | GAGTCTCGTGAGATA[A/G]TAGAGCAATAGAGTC | 9100 |
| rs186461324 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84725705 | CACCGTGCCCGGCCT[C/G]TCTGACGACATTTTC | 9100 |
| rs186463352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84713027 | AGCAAATGCAGCTGT[C/T]CCCCAAATGCAAGAA | 9100 |
| rs186466717 | snp | C/G/T | 0.00159649 | 0.0282165 | intron-variant | USP10 | GRCh38.p7 | 16:84700646 | TCTGTTTTTTAGATA[C/G/T]AAGTAGCAGAGTAGC | 9100 |
| rs186517065 | snp | A/C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84729760 | CGTGTATTTTGATGG[A/C/G]GTTGTTTTTTGAGCT | 9100 |
| rs186529458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84778696 | CTTACCTTGCAGTTA[C/T]AGAAAAGTTTTTATT | 9100 |
| rs186530847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751926 | ATAGCTTATGATGAC[A/G]TAAAAGTTTACGATG | 9100 |
| rs186571736 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84738940 | GCCGTTCCTGCACTG[A/G]CCTTTGTACTGCAGT | 9100 |
| rs186650008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84722621 | GGCTGGAGTGCAGTG[A/G]TGTGATCTTGGCTCA | 9100 |
| rs186662350 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84777004 | TTTGAATAGAGACGA[A/G]GTTTCGCCCTTTTGG | 9100 |
| rs186694064 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84747119 | GACCGAAATGTTACG[A/C]CGCGCGTGACTGTAC | 9100 |
| rs186724162 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84741336 | TGAAGCTTGAGGGAC[C/T]GGGAAGCCGGGCTGC | 9100 |
| rs186730285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84716634 | AAGTAGGACTTCTTC[A/G]GAGCATGGGGGAAGA | 9100 |
| rs186732736 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84720413 | GTTTTTGGCAGTAAT[C/T]GTCTTTGTGTGGAGT | 9100 |
| rs186733544 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698597 | TTCTTTCTTTCTTTC[C/T]TTCTTTTTTTTTTTT | 9100 |
| rs186736774 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84708657 | GTCACTTTGTTTCAT[C/G]AGAGTACTGCAATGG | 9100 |
| rs186766480 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84765179 | TATTTAAAGTATACA[C/T]AGATGTTATGAAATA | 9100 |
| rs186875111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751604 | GTTGATCTGTAGTCA[A/G]TGGGTAGTGGTACAT | 9100 |
| rs186880746 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84710283 | GGAAAAAAAAAAAAA[A/C]AAAAGATTGCTGGGT | 9100 |
| rs186907944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84735281 | TGTATTTTTTCCCAC[A/G]TCACACTGATGTAAC | 9100 |
| rs186989642 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84720784 | AGACGGGGTTTCACC[A/G]TATTAGCGGGGATGG | 9100 |
| rs186990018 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84708760 | AATAGAATGCAAAAT[C/T]GGGGCTTCCAAGTGT | 9100 |
| rs186990448 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84758022 | TTCTGATGGTTAATT[C/G]TATAAAGATGGCATT | 9100 |
| rs187005378 | snp | A/G | 0.000255102 | 0.011291 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745549 | CTCTTCCTCCTCGCC[A/G]GTGGCCTATGTGGAA | 9100 |
| rs187027608 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | USP10 | GRCh38.p7 | 16:84734201 | GAGACTGCTCGTTTG[C/G]TATCTAGGATTTTAA | 9100 |
| rs187043548 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84716065 | AAGCAGGGCTCCCAT[C/G/T]TGGCCTGGGGGTGGG | 9100 |
| rs187118793 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84770504 | TTGGCTGGGCGAGGT[C/G]GCTCACACCTGTAAT | 9100 |
| rs187125419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84755717 | GCACAAGAATTGCTT[A/G]AGACCCAGAGGCGGA | 9100 |
| rs187178165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84747512 | AATGATAGGCCAGAC[A/G]TCGTTATTTTGGGCT | 9100 |
| rs187215468 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP10 | GRCh38.p7 | 16:84773187 | GAAAGCAATTTTAAA[A/G]AGCCCCAGGTTAAAG | 9100 |
| rs187239182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84704481 | CAGCAGTGTAGATGT[C/T]CATTTCCAGAGACTT | 9100 |
| rs187262613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84773538 | GCCCTATACCTTCCC[A/G]TGAAGACTCAGACAC | 9100 |
| rs187281582 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84758328 | TCTATCTAGTGTCTG[A/G]GGCGCCTTGCTGCTG | 9100 |
| rs187288281 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84705471 | CTCCTGACCTCACGA[C/T]CCGCCCACCTCGGCC | 9100 |
| rs187305206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84730072 | AGTATGTAGTCCCCT[C/T]CCAAGAAAACCCTCC | 9100 |
| rs187319725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84711379 | ACTCCCCCACAGCTC[A/G]GTGTAACTGTGAGCA | 9100 |
| rs187322505 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84716710 | GCAGAGTTACTGGGA[C/T]CTTAGGTGCACGACC | 9100 |
| rs187335547 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84748290 | TTCTAAGTTCGAAGT[C/G]ATGAGAATTTTATTT | 9100 |
| rs187341999 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84723422 | ATGAAAGATGTACTC[C/G]TAGCTGGAACATCTC | 9100 |
| rs187342127 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP10 | GRCh38.p7 | 16:84737035 | CCTCGTGGTCTGCCC[A/G]CCTCGGCTTCCCAAA | 9100 |
| rs187377677 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84749469 | TAGACATTAAATGTA[A/T]TCCTTTCTGCCAGGC | 9100 |
| rs187397885 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | USP10 | GRCh38.p7 | 16:84774711 | TCCTGACCTCGTGAT[C/T]GCCCGTCTCAGCCTC | 9100 |
| rs187426230 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84766212 | AGAAGCTGGTTTCCC[A/G]TCCTCTGTGGAAGTG | 9100 |
| rs187437070 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84752017 | AGCTACCATCTAGCA[A/T]GTATGTCTTAAAATT | 9100 |
| rs187532551 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84700954 | TCTGGACAAAAATCG[G/T]CATGATGTATTATTT | 9100 |
| rs187559485 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84752143 | AAAGTGAACTACAGG[A/T]TTCAATTTTGTGTCT | 9100 |
| rs187564251 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84766485 | CTGTGCCCTTTGCTC[A/C]TTCAGCCCAGCAGCC | 9100 |
| rs187656961 | snp | A/G | 0.000265292 | 0.0115141 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744758 | CCTGAATTTATTCTC[A/G]GTTGTACAGCTTCCA | 9100 |
| rs187666097 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84761436 | GGTATACCCGTGGCT[A/G]TGGTTGCTGACAGCA | 9100 |
| rs187666709 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84770269 | TCAGGAAGATTTGGG[A/G]CAGCTTGTATGGAAG | 9100 |
| rs187725107 | snp | C/T | 0.000822707 | 0.0202652 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779320 | ATTTTAGAAAATACA[C/T]AAAAACCCATATTTC | 9100 |
| rs187778660 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84710926 | TCGCATGAATAGCAA[A/T]AACGAAATCGTATTT | 9100 |
| rs187781042 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84723248 | GTAATTGTTAATGAT[G/T]TTTCTTTAGGTCAAA | 9100 |
| rs187786443 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84739366 | AACCTCCATCCCCCA[A/G]GTTCAAACGATTCTC | 9100 |
| rs187795217 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698691 | ACCTCCGTCTCCGGG[A/G]TTCAAGTGATCCTCC | 9100 |
| rs187830856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84762519 | GACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 9100 |
| rs187864283 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84713575 | TGTTTGCTTTGTTCA[C/G]TGCTGGGGCCCCTAG | 9100 |
| rs187871677 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84750131 | AACTTAATACAGCCC[G/T]GCACAGTGGCTCACG | 9100 |
| rs187907115 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84702445 | TAGTTACTGGTTCCT[C/G]CTCCAGTCATTCTGA | 9100 |
| rs187925028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84755114 | GTTTTTGAGTCTGTT[C/T]GAACGGGTCAACAAC | 9100 |
| rs187930941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84754743 | AATAAATGCTGGGAA[A/G]AAAGTCGGTTTATAG | 9100 |
| rs187933760 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84733820 | TCCTGACTGGTTTTC[A/C]CCTTTTATCATATAC | 9100 |
| rs187935019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84727443 | TAACCTCACAATTTT[C/T]AGTGTTAGCTTTAAA | 9100 |
| rs187935169 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84739498 | GACTGGTCTAGAACT[A/C]CTGACCTCAAGTGAT | 9100 |
| rs187942126 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84769722 | CCACCCATGCTGTTG[A/G]GGAGGTGGTCAGCCT | 9100 |
| rs188013521 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84774419 | TAGCAGCTGGTAGAC[C/T]GGTTCCTATTTGGAG | 9100 |
| rs188083710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84752654 | TTTTGCATGATAACA[A/G]TAGGATTCATTCACT | 9100 |
| rs188086492 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84726379 | GAGGAATGTGTCTTT[A/C]TTGCTGAGGGCAAGG | 9100 |
| rs188096628 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP10 | GRCh38.p7 | 16:84731056 | TCATTCTCGGCTTGC[C/T]GCAACCTCCACCTCC | 9100 |
| rs188104154 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84749877 | TCCTCGGTGTAGGTT[A/G]TGTGTCAACATTTTG | 9100 |
| rs188106625 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84775358 | GTGGCCTTGTGAGTC[A/G]GGGAGTCACGTGAGA | 9100 |
| rs188107059 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779839 | GCTCTTCTCTAATGC[C/T]GCGTCCCTAATTGTA | 9100 |
| rs188148539 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84701631 | TCTTTAGGCATAGCT[C/G]ACTTCCTTTATTTAA | 9100 |
| rs188210480 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84709212 | TACGTACACGTCACT[C/G]CAAACTGAGAGATGT | 9100 |
| rs188230551 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84734703 | TTAAAAATATCTTTA[C/G]GAAATTCTTCCCATC | 9100 |
| rs188234624 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84763768 | TGTTGTGATTGGTTG[A/C]CGTGGATCCAGTGAC | 9100 |
| rs188246208 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84739701 | TTTCAGCTTTTTACA[A/G]AGAAGTCAGACAGTT | 9100 |
| rs188249763 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84721854 | AGGCACACGCCGCCA[C/T]ACCTGGCTAATTTTT | 9100 |
| rs188251408 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84750966 | AACAAAGTTATTACA[A/G/T]TTTGGGTCTTCTCTA | 9100 |
| rs188275568 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84731120 | GAGTAGCTGGGACTA[C/G]AGGTGCATGCCACCA | 9100 |
| rs188311722 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699113 | TCTCTTGGCCAGTGT[A/G]CTCACGTTAATCTAA | 9100 |
| rs188382422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84742025 | GCAGAGGCACCTCAT[C/T]GTGGCTTCCCTTTTA | 9100 |
| rs188402766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84767149 | AGAAAAGCTTTTAGC[A/G]AGCTCTTCACCGCAT | 9100 |
| rs188428651 | snp | A/G | 0.0119091 | 0.0762411 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698900 | GCGCCTGGCCCACTT[A/G]TATTTTTCATGGCAT | 9100 |
| rs188438126 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84723748 | GGTATAACGTATGTG[C/T]GGTGAATTTCACCCA | 9100 |
| rs188472877 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84773834 | TCCTGCATCTTCACT[C/T]GCCTCCAGATCAGCT | 9100 |
| rs188524671 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84757439 | TGTGTGTGTGTGTGT[A/G]TGTGTGTTTTGAATT | 9100 |
| rs188529294 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84703301 | TACACCGAAAAAATA[C/T]TTGTGATTATTGATG | 9100 |
| rs188535250 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84772083 | CTGAGACAAGATCTC[A/G]CTGTGTTGCCCAGGC | 9100 |
| rs188588956 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84711601 | ATTACGCTTGGTTCT[C/G]TGTTGCTTCTTACCT | 9100 |
| rs188593723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84736678 | GCACACATCCCAACC[A/G]TGACTGAGTCAATAA | 9100 |
| rs188596173 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717257 | GCATTCTTTAGGGGG[C/T]GGGCCTAATTCCCTT | 9100 |
| rs188645867 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84724469 | AGACACTCAATTGCA[G/T]TACTTTGACATTTGA | 9100 |
| rs188652642 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84738048 | TGGTTGAATGTTGAG[G/T]AAGGGGACAGCCGGA | 9100 |
| rs188672888 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84760329 | CCTTTTGTTCCAGTG[G/T]TTGTGTGGTAACTGT | 9100 |
| rs188714567 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84737566 | GCATTCCTGCAGGTG[C/T]GCTCTTTTATCAGCT | 9100 |
| rs188745954 | snp | A/G | 0.000820436 | 0.0202372 | intron-variant | USP10 | GRCh38.p7 | 16:84778857 | TGATTCGTGTGCAGT[A/G]CTGTTCTCACTCTGC | 9100 |
| rs188752457 | snp | A/G | 4.96857e-05 | 0.00498401 | synonymous-codon, nc-transcript-variant, intron-variant | USP10 | GRCh38.p7 | 16:84758750 | CCTAATCCATAAACC[A/G]GTGTCGTTGCAACCC | 9100 |
| rs188862785 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84706446 | TTTAAGTAATAATTT[C/G]CCTTACGTGGCTGCA | 9100 |
| rs188870137 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84730615 | CCACTTGGTGTCTGC[A/G]TTTGAAACAGGAAGT | 9100 |
| rs188880406 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | USP10 | GRCh38.p7 | 16:84706019 | GAGCCACTGCCCCCA[C/G]CATCCCTACTCATTC | 9100 |
| rs188890359 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84776115 | TTCCTTACATGTGTC[C/T]TAGGAGATGGGAGGT | 9100 |
| rs188932300 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84733021 | GATTTCCTTGTCTTC[C/G]CATTTGAACCACGTT | 9100 |
| rs188940313 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | USP10 | GRCh38.p7 | 16:84764484 | AGGGGACAGGGAGCT[A/C]CTCCCTTCTACTCTG | 9100 |
| rs188948813 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84708362 | GGCTGAGGCAGGAGA[A/C]TAGCTTGAACCCGTG | 9100 |
| rs189090902 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84767389 | CAAGGTCAAATTGGC[A/G]CCCTTCTTGGAAGGG | 9100 |
| rs189095742 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780277 | GCGGTGCCTCCAGAC[A/G]CCACCCTCAGTAGTG | 9100 |
| rs189128639 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | USP10 | GRCh38.p7 | 16:84706748 | GGTTTCACGGTGTTA[A/G]CCAGGATGGTCTCCA | 9100 |
| rs189132261 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718238 | GTTCAGAAGACATTT[C/G]TGAAGAGTTGCTTGT | 9100 |
| rs189143639 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699329 | GAATGAACCAACGAC[C/T]CCCAAGGCTGGTTTG | 9100 |
| rs189148149 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84742400 | ATGTTTTCATTCTCA[G/T]TTGTTTGTATTTGTC | 9100 |
| rs189157181 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84763395 | ACATATTTTCTGATG[C/G]TATACACACACTGTG | 9100 |
| rs189158354 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84753361 | ATGCTGAAAGTTGTT[A/G]GTTTTCTCAGACTCT | 9100 |
| rs189160216 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84731503 | TTCTGGAATTCTTAA[C/G]CAGTTTCCTTTCCTC | 9100 |
| rs189168152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84738011 | GGGAGTGGCTGGGAG[C/T]TGAGTGAGTGTTCAC | 9100 |
| rs189175865 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84723894 | TCTTCTTTTGTTCGT[C/G]CTTGGCCCCAGCAAA | 9100 |
| rs189177276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84711803 | CAGCTCACTGCAACC[C/T]CTGCCTCCGGGGCTC | 9100 |
| rs189188084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84746351 | TCCTCACATAGCCAC[A/G]TGTTGCTTAACTAAG | 9100 |
| rs189192268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84771688 | AGCCTGGCCAACATG[A/G]TGAAACCCCTTCTTT | 9100 |
| rs189223266 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84727814 | CCTAAGAATAGGCAT[A/G]TTCTCTTAAATAACC | 9100 |
| rs189241632 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84703090 | TATTAGAAAGTGTTG[A/G]TTGATCCCTGTTACC | 9100 |
| rs189254519 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84743996 | GGAGGAGACCAAGAG[A/G]TAGAGAATTCAGAAG | 9100 |
| rs189293372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84748774 | GATAAATAGTTTGTT[A/G]TGTTCTGTATATGTT | 9100 |
| rs189466547 | snp | C/T | 0.00400466 | 0.0445678 | splice-donor-variant | USP10 | GRCh38.p7 | 16:84768360 | AAACCAAACAAGAGG[C/T]ATGTTCACACTTGAT | 9100 |
| rs189479070 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84757140 | CACATGACAGGTGCT[A/C]TCTCTGCTGGGTGTC | 9100 |
| rs189521925 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84715110 | CTTTTTATATTTTTT[A/T]GTAGAGATGGGGTTT | 9100 |
| rs189533036 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84763950 | ACGTTGCTCCTGTTG[A/C]GATTGGTTGCCGTGG | 9100 |
| rs189544287 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84740064 | TTCATTTTTATTCCT[G/T]TTGGCTTCATTTTCG | 9100 |
| rs189575201 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84715868 | TTATCCCAGGGCTAG[G/T]TTCCCCCACGATGGC | 9100 |
| rs189594827 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84751642 | ACTTTGCTGTCCTCC[A/G]CCTGGTTAGATAACC | 9100 |
| rs189605638 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84728348 | TTGAATAAATATTTG[A/G]CCTTTTTTACTTTTT | 9100 |
| rs189609631 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84741016 | ACAATTCAAACTTGT[C/T]GAGATCATTTTTCAA | 9100 |
| rs189611866 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84770863 | ACAAAGTCAAGAGAT[C/T]GAGACCATCCTGGCC | 9100 |
| rs189685493 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84728205 | CTGAATTTCTGTGAT[A/G]AACTTTTTGGTGTCA | 9100 |
| rs189705815 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84712299 | GAAGACATGGCTCTG[C/T]CTGGGGAGACTGTGC | 9100 |
| rs189713519 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84749847 | TACTTGGACCTTCTT[C/G]GTGGCAAGGCCATCT | 9100 |
| rs189742741 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84761922 | TGCCCTTTTCTGCAC[A/C]CGTGCAGAGCATGCA | 9100 |
| rs189797730 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84751305 | GAACATATCCCCATC[A/G]TTAAGCATGGCTGTG | 9100 |
| rs189823936 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84777063 | AAATGAGGTCACCGG[A/C]CTGGTTAGAATTACC | 9100 |
| rs189854743 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | USP10 | GRCh38.p7 | 16:84711271 | AAAATGTAAGTACAC[A/G]TGTGTTCCCCAGAAC | 9100 |
| rs189856367 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84723323 | GTTGAATAAGTCTTA[C/T]ATTTTAAAATATAAG | 9100 |
| rs189865029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84778190 | CTACCAGCACCATCT[C/T]CGCAGTGCCCCACCA | 9100 |
| rs189868993 | snp | A/C | 0.00478085 | 0.0486577 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698759 | CCACACTACATCCCA[A/C]CAATTTTTGTATTTT | 9100 |
| rs189872739 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | USP10 | GRCh38.p7 | 16:84747621 | AGGCTGTAGTGCAGG[A/T]GGCACGATCTTGGCT | 9100 |
| rs189885349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751783 | TGTCGATTACGGGCC[A/G]GTTATTGAGCCCTAA | 9100 |
| rs189891156 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84778370 | GTATTCCCGCATCAC[A/C]ATTCTTAATCTATTC | 9100 |
| rs189893371 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84764683 | TAAAAATACAAAAAT[A/C]AACCAGGTGTGGTGA | 9100 |
| rs189895273 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84736756 | TGTGTGTGGGTACTC[A/C]TGGAGAGTAGAGAGT | 9100 |
| rs189989098 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84749316 | GCAGCGTTTAACTGA[A/G]TGAAAGTCTAGTTTC | 9100 |
| rs190019397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84774595 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGAGACTA | 9100 |
| rs190020673 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717924 | ATTTTGTTGAGATGG[C/T]CCCAGAAATTTGGGA | 9100 |
| rs190024693 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699567 | TGAATGCGCGGCAAC[A/G]GGATCTTCATAAACC | 9100 |
| rs190056385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84704927 | TCGACTTTCCCTTTT[A/G]GGCTCACATGAGAAT | 9100 |
| rs190062960 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84722212 | ACAAACTGTACTCTT[C/T]TGTTTGGTTACCTTC | 9100 |
| rs190063260 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84735102 | TGCAATCACAATTCA[A/C]TGCAACTTTGACCCC | 9100 |
| rs190074022 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84724928 | ATTGTTCAGTAGATA[A/C/T]CAGCTAGCACCCATA | 9100 |
| rs190095855 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84716638 | AGGACTTCTTCAGAG[C/T]ATGGGGGAAGAGGGA | 9100 |
| rs190208497 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84707428 | CACGAAAACAGCACA[A/G]ACGTATTTAAAGTGA | 9100 |
| rs190241777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719212 | GTTGTTCATCAACTT[C/T]ATATAGTGAGTAATT | 9100 |
| rs190250922 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84760397 | AGTAGATGTAGGTTT[A/G]TAAGAGTCCATTGCT | 9100 |
| rs190253208 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84738775 | CTTACTGCGTTACTA[G/T]CAGAGAGAAGCTTTT | 9100 |
| rs190314452 | snp | C/T | 0.000151468 | 0.00870121 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779084 | TGGACCTGCTGTAAA[C/T]CCTGTGTGCGCTGTG | 9100 |
| rs190345620 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84742706 | GAGCTCTCTGCCATG[C/T]GGTGCAAGGCACATG | 9100 |
| rs190353332 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718755 | AGCAAGACTGTCTGA[C/G]AAAAAAACAAAAAAA | 9100 |
| rs190359480 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84759791 | TACCTAAAATCTACT[A/G]TACTCGTATAGCTGA | 9100 |
| rs190382325 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84766451 | GAGGTCCAGGTTGGC[A/G]CGCAGCAGCGAGGGA | 9100 |
| rs190392629 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741553 | CAGTGGGCACCACCA[G/T]CTCCCCCAGCCTCTG | 9100 |
| rs190399040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84752031 | ATGTATGTCTTAAAA[C/T]TTGAAAAAAGGCTAT | 9100 |
| rs190472569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84706937 | TACGAGATACTAAGC[A/G]TTGTAGTAGTCATCA | 9100 |
| rs190490129 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84734486 | AATCAAGTAGCTTGT[C/T]TTTTTCTTACTGATT | 9100 |
| rs190510252 | snp | A/G/T | 0.00517822 | 0.0506191 | intron-variant | USP10 | GRCh38.p7 | 16:84732640 | TTAGTAAAGATGGGG[A/G/T]TTTCACCATGTTGGC | 9100 |
| rs190520353 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719592 | CTCCCCTGCTAGGTG[A/T]GTACCACCGCGGATT | 9100 |
| rs190522344 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84708119 | TGAAGACTTCCACCC[C/T]CTTAGTAGTAGTCAT | 9100 |
| rs190529055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84756590 | AGAGCAAGACTTGTC[C/T]CAAAAAAACAAAGGT | 9100 |
| rs190534951 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84769076 | ATCTTAGGTTGTGGC[A/C]GTGAATTCATAAAAA | 9100 |
| rs190547399 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | USP10 | GRCh38.p7 | 16:84754663 | CTGGAAGCTGGTATC[G/T]ATTTAAGGGAATGGC | 9100 |
| rs190562064 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84709122 | GAGTGATGAGCGAAA[A/T]CAGGCATTGTTTCTC | 9100 |
| rs190603707 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84774015 | AGCACTTTGGGAGGC[C/T]GAGGCAGGCAGATCA | 9100 |
| rs190607510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84731802 | GTGATAGTCTGTGCT[A/G]ATTTTTTCTGCTTCC | 9100 |
| rs190624861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84754193 | GAGAATCTTGAGTGC[C/T]TTCTGTCGGTCTTAC | 9100 |
| rs190639407 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84739263 | ACAGGGTTTGTTTTT[G/T]TTTTGTTTTGTTTTG | 9100 |
| rs190651933 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84754591 | GACTTGATTTTAATA[C/G]TGTGCAAGAAAAACT | 9100 |
| rs190751301 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | USP10 | GRCh38.p7 | 16:84721156 | CTGGGCCTCCCAAAG[G/T]GCTGGGATTACAGGT | 9100 |
| rs190805840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84729240 | TTTATCACATCATTC[A/G]TAATCCATGTTTGAA | 9100 |
| rs190862569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84704512 | GTATGTGCTTGGACT[A/G]CAGTTTTCCTGTTTA | 9100 |
| rs190888402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84768630 | TTTCTGGCAATCTAA[C/T]GATGATATCACAACA | 9100 |
| rs190897952 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84725876 | TTTCATGTTTCCCCA[A/G]ATTGAGCTTATTTGG | 9100 |
| rs190934502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84773440 | TGGCACAGCAACCCC[A/G]CCTCATACCTCCTTC | 9100 |
| rs190949965 | snp | A/C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84761547 | GGGGCCACAAGGCTA[A/C/T]GCGTAACTACTCCAG | 9100 |
| rs190997912 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84713029 | CAAATGCAGCTGTCC[C/G]CCAAATGCAAGAACC | 9100 |
| rs191000561 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84700831 | TACAATAATCCCGTG[G/T]TGGAAAGAAAGAGCT | 9100 |
| rs191005532 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698508 | AAGCAAGATGACACA[C/T]TGTATTTGGTTATGT | 9100 |
| rs191028893 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84725711 | GCCCGGCCTGTCTGA[C/T]GACATTTTCAAACCC | 9100 |
| rs191031125 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84741270 | GAAATGTGGGAGACC[A/G]TAAGGGAAAGAGCAG | 9100 |
| rs191035136 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84739021 | CTGCCCTCAGGTAGC[A/T]GTTTATCTCTCTGCT | 9100 |
| rs191063811 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84758067 | TACACAGAAAGAGTG[A/G]TGTCCACTCAGGGTG | 9100 |
| rs191081392 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84765627 | ACAGCTGAATAGTGT[A/T]CCCTTGTCTATATAT | 9100 |
| rs191094673 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84763808 | GTTGCGATTGGTTGC[C/T]GTGGATCCAGTGACG | 9100 |
| rs191111477 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84716185 | GTCTCTCCCCCCTCT[C/G]CTTTTCCAGATATGC | 9100 |
| rs191119148 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84777045 | AGCCTATTCTGATCT[G/T]GGAAATGAGGTCACC | 9100 |
| rs191168453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741410 | CAGACATCTGAGTCA[A/G]TGGGACTTCCTCTGT | 9100 |
| rs191286945 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | USP10 | GRCh38.p7 | 16:84720548 | CAGTTAAATTGAAAA[C/G]AGATGCAGAATAAAA | 9100 |
| rs191294844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84708691 | AAAACAAAACACTTC[C/T]CAACTCAGGTCCCAC | 9100 |
| rs191306276 | snp | C/G | 0.000534572 | 0.0163401 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745371 | CCTCGGGTGAGGGCA[C/G]AGCTACCAACGGGGT | 9100 |
| rs191311525 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84713261 | AGGGGAACACATTGT[A/C]TGTCCCCGAGACCCT | 9100 |
| rs191313658 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84732159 | AGGAGGGTATTACAT[G/T]TAGTGGCCATTTATT | 9100 |
| rs191317003 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84733937 | TTAAGCTAACGTTGT[A/G]TTCTTTATGCTAAGA | 9100 |
| rs191338457 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84778719 | TTTTTATTATGGATT[A/C/G]CTTGCGTGTTTGAGT | 9100 |
| rs191340330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751938 | GACATAAAAGTTTAC[A/G]ATGCTGGTATTGCCT | 9100 |
| rs191396619 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84710171 | GCTACTTGAGAGGCT[G/T]AGGCAAGAGAATCGC | 9100 |
| rs191401035 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84729941 | CCTAAGCTGTTGTCA[A/G]TGAGCTCTTGAAACT | 9100 |
| rs191434191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84723900 | TTTGTTCGTCCTTGG[C/T]CCCAGCAAAGATAGA | 9100 |
| rs191439498 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP10 | GRCh38.p7 | 16:84757791 | GGCTCCTGTGTGATC[A/G]CAGGTGAGTTAGTCA | 9100 |
| rs191442075 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP10 | GRCh38.p7 | 16:84738026 | TTGAGTGAGTGTTCA[C/T]ACCCCGTGGTTGAAT | 9100 |
| rs191449912 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84735370 | CCTGTTTGCAAGTGA[C/G]TAGACAAAAACTTGA | 9100 |
| rs191454621 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84759825 | TCTACTTAGCCATCA[A/G]AGCTCTTTAGTAAAA | 9100 |
| rs191460583 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779647 | GAGAAACTGCTTACG[G/T]ACACATTGCAGATCA | 9100 |
| rs191558528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84743076 | GCCTTGACGGCCCCA[A/G]AACATCAGGGAATAG | 9100 |
| rs191689599 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699862 | CGGGGCTCAGAGTCC[C/G]GCAGGCTCCAGGCGG | 9100 |
| rs191691913 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717950 | TGGGATTCGTGATCA[C/T]GTTAGGGTATTTGTG | 9100 |
| rs191706468 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84706453 | AATAATTTCCCTTAC[A/G]TGGCTGCAAAGACTA | 9100 |
| rs191707635 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84747237 | TTAAAATAAGCTGTT[G/T]GGTTTAGGCTTTCTG | 9100 |
| rs191709979 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84737366 | AACTTTGTATTCTTA[C/T]AAATAGTTATATAGT | 9100 |
| rs191718322 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84773150 | CTCAAGTCTCTGTCA[C/G]GTCACGGGCTCGGCA | 9100 |
| rs191728924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84758333 | CTAGTGTCTGAGGCG[C/T]CTTGCTGCTGATGAG | 9100 |
| rs191730551 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | USP10 | GRCh38.p7 | 16:84731171 | TTTTTAGTAGAGACG[A/G]GGTTTCACCGTGTTA | 9100 |
| rs191735576 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84773809 | CAAAGAAGGCATCCT[C/T]GGCCTCTGCTCCTGC | 9100 |
| rs191754741 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84775627 | CCCAGCCGGTGATCC[C/T]TGCGTCCTCCCCCAC | 9100 |
| rs191900017 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84744058 | TTCTTTGTTGTTGTT[C/G]TTGTTGTTGTTGAAT | 9100 |
| rs191914457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84769883 | GCAGGTAGTTGTTAG[C/T]CTGTTGTTAGACGGT | 9100 |
| rs191933526 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84730211 | CAGTGTCTCTTTATG[A/C]AGACACAAATATCTA | 9100 |
| rs191939308 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699154 | ACAGAAATCTTACGC[G/T]TTATGACATATTTGT | 9100 |
| rs191947010 | snp | A/T | | | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719893 | ACTGAGACAGCAAAC[A/T]GTGGATTCCTTCCTT | 9100 |
| rs191953757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84716775 | ACCAAGTTGAAGAGT[A/G]AAGATTCTACCTTTA | 9100 |
| rs191971797 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84712728 | GAATGCATGAGTGAC[C/G]CCTAAGCTGCTCTTC | 9100 |
| rs192075813 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84710547 | AAGGTCATTTAGGGA[A/C]ATATTCCCTTTATTT | 9100 |
| rs192107861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84701696 | GTTAATTAATGGGGA[C/T]GGATAATATGTAAAC | 9100 |
| rs192189266 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84754837 | ATTCTGGGCCCCTAA[C/G]TCAGTTAAGAACATG | 9100 |
| rs192211677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84755401 | GTCTCCTTCCTCAGC[C/T]CGGCTTCTGGCTGAG | 9100 |
| rs192216858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84715141 | CACCATATTGGCCGG[C/T]CTGGTCTCGACCTCC | 9100 |
| rs192274954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84733050 | TTTTCTGCTTTTCTT[C/T]AGTATGTTTGGCAGA | 9100 |
| rs192279550 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84708437 | GCCTGGACGAAAGAG[G/T]GAAACTCCATCTCAA | 9100 |
| rs192309750 | snp | A/C/T | 1.84975e-05 | 0.00304112 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745593 | CTCCCGCCATATCTC[A/C/T]CCTGGTTTCTGAAAA | 9100 |
| rs192326103 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84734474 | TCCATATTTTTAAAT[C/T]AAGTAGCTTGTCTTT | 9100 |
| rs192327884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84770736 | GAGATAGCGCCACTG[C/T]AGTCCGGCCTGGGCG | 9100 |
| rs192339932 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84755969 | TGGATAGCACTGCTG[C/T]CCCAGTCAGTGAGAA | 9100 |
| rs192354804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84730710 | AAATCATTTGGATTT[A/G]TAGTGTTCTTACTGG | 9100 |
| rs192372236 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84706287 | AGTTCAATTCTAGAG[C/G]TTTTCGAGATTCCTG | 9100 |
| rs192400516 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | USP10 | GRCh38.p7 | 16:84727451 | CAATTTTCAGTGTTA[A/G]CTTTAAAAAAACAAA | 9100 |
| rs192404418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84739531 | ACCCACCTCAGCCTC[C/T]CTCATTGCTGGGATT | 9100 |
| rs192408124 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84714761 | CCTTAATTCATTGAT[C/T]ATTTTTGGGGTGAAG | 9100 |
| rs192423804 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84763437 | ATGTCTTATCTGTCC[A/C]TCCATATATACATAC | 9100 |
| rs192428263 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84722725 | CCCCCACGCCCAGCT[A/G]ATTTTTGTATTTTTA | 9100 |
| rs192433414 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | USP10 | GRCh38.p7 | 16:84776615 | GGTGGCCAGCAGTTT[C/G]TCCGCCTTCTCCCTG | 9100 |
| rs192441082 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84750269 | AAAAATTAGATGGAC[A/G]TGGTGGCTCATGGCT | 9100 |
| rs192472266 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84752461 | CTCTATCCTTGGTGG[C/G]CCGCCTTCCTCATTT | 9100 |
| rs192473038 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84702869 | GTGGTGAAGCTCGCC[C/T]GTAGTCCCAGGTACT | 9100 |
| rs192513149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84774340 | ACAGCATGCCTCCGA[C/T]GGACTCTTGTGTCGG | 9100 |
| rs192521184 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84770409 | AACATGTGAAGGTTT[G/T]GGGGAAAATAGGATT | 9100 |
| rs192539536 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84751253 | ATCTAGGCATGTGAT[C/T]CCACAATGACAAAAT | 9100 |
| rs192616565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84727839 | ATAACCACAGTAATA[C/T]GTTACCACTTTCACA | 9100 |
| rs192629019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84703239 | TGTCACTGAGGGGAC[C/T]GGTTAAATTATTTGG | 9100 |
| rs192635013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84705560 | TGAACCTGATTTTTA[C/T]ATCTAGCTGACTCCT | 9100 |
| rs192640396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84723622 | GAATTCATTTGTTCA[A/G]CAAAGCTATTTTGAG | 9100 |
| rs192665660 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84742058 | TCTCGGCCTTTTCTA[G/T]TTTTGTGTTTTTTAA | 9100 |
| rs192702657 | snp | A/G | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698986 | CTGTTCATCTCCTCT[A/G]CTCAGTGTACGGTCT | 9100 |
| rs192724691 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717278 | TAATTCCCTTACATC[A/G]GTTTCTCGGGAGGTC | 9100 |
| rs192738114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84767157 | TTTTAGCGAGCTCTT[C/T]ACCGCATCTGTTCTG | 9100 |
| rs192797824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741902 | TGTGTCTGTCACTGC[A/G]CCTGTAGTATCTGGA | 9100 |
| rs192814695 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84758918 | CTCTCCATTTGAATC[C/T]CTAAGTCTGGTTTAT | 9100 |
| rs192831183 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84711640 | TTCTGTGCCACAACA[A/T]TGTATTCTAAGTTAG | 9100 |
| rs192842109 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84737850 | TGCCCAGTCAGTGCC[A/T]CCTGGTGTCACTGGT | 9100 |
| rs192880257 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84752750 | GCGAGGAAGAAGAGG[A/C]GCTCACGAACTTCAT | 9100 |
| rs192901158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84711408 | CATCTGATGTCCCAG[A/G]GAACTGGAACTTTAT | 9100 |
| rs192925934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84726913 | ACTGCTTTCTGATAC[C/T]TCCTTTTGACCCCAG | 9100 |
| rs192938476 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779889 | GGAGTATAAAGTTGT[C/T]GCCCATCAATAAAAA | 9100 |
| rs193019224 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | USP10 | GRCh38.p7 | 16:84748565 | TGCCTCAGCCTCTCA[A/C]AGTGCTGAGATTACA | 9100 |
| rs193021444 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84773854 | CCAGATCAGCTGTCT[C/G]AGCTGACTTGGATGT | 9100 |
| rs193059298 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84723768 | AATTTCACCCATTTA[A/T]AGTGTATATTTCCAT | 9100 |
| rs193116957 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84771520 | AACAAACAAAAAAAC[C/T]CACCTAATCCTACTG | 9100 |
| rs193163493 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | USP10 | GRCh38.p7 | 16:84739432 | GCCTGCCACCACGCC[C/T]AGCTGATTTTTTGTA | 9100 |
| rs193166036 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84713713 | GCTAGAGAATCAACT[C/G]TTAGGATCCAGAATT | 9100 |
| rs193196465 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84720807 | GGGGATGGTCTCGAT[C/T]TCCTGACCTCATGAT | 9100 |
| rs193197836 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84762672 | CTCCAGCCTGGGTGA[C/T]GGAATGAGACTTTGT | 9100 |
| rs199525709 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84735221 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 9100 |
| rs199532803 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84728403 | GGAGTTCAGTGGTGC[A/G]ATCTCGGCTCACTGC | 9100 |
| rs199541791 | snp | A/C/T | 8.30163e-05 | 0.00644221 | intron-variant | USP10 | GRCh38.p7 | 16:84733523 | GACAAAACTTTGTTT[A/C/T]AGTGAGTCCGTGGGT | 9100 |
| rs199578651 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84764939 | AGAGAGAGAAAAAAA[A/T]ATATATATATATATA | 9100 |
| rs199587707 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84746166 | TCAGCTCTTGAAGAG[A/G]AAAAAAATGTTAAGG | 9100 |
| rs199626978 | snp | C/T | 0.0039921 | 0.0444985 | intron-variant | USP10 | GRCh38.p7 | 16:84733522 | AGACAAAACTTTGTT[C/T]TAGTGAGTCCGTGGG | 9100 |
| rs199630950 | in-del | -/C | 0.0130921 | 0.0798413 | intron-variant | USP10 | GRCh38.p7 | 16:84702804 | TCGAGATCAGCCTGA[-/C]CAATATAGTGAGACC | 9100 |
| rs199654727 | snp | A/C | 0.000874049 | 0.0208869 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745637 | AAAGAAGGGCTTGTT[A/C]CGGTTTCAGAGGATC | 9100 |
| rs199663831 | in-del | -/T | 0.293807 | 0.246132 | intron-variant | USP10 | GRCh38.p7 | 16:84739257 | GTTTGTTTTTTTTTT[-/T]GTTTTGTTTTGTTTT | 9100 |
| rs199738029 | snp | A/G | 0.000165741 | 0.00910182 | synonymous-codon, nc-transcript-variant, intron-variant | USP10 | GRCh38.p7 | 16:84759389 | ATTGGTTGCTTGCCC[A/G]CCGATGTACCACCTG | 9100 |
| rs199788392 | snp | C/G | 1.65886e-05 | 0.00287993 | missense, nc-transcript-variant, intron-variant | USP10 | GRCh38.p7 | 16:84759382 | TGCAGGCATTGGTTG[C/G]TTGCCCGCCGATGTA | 9100 |
| rs199880133 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84723159 | GGTTTTTTTTTTTTT[-/T]GGCCTTTTTTCCCCC | 9100 |
| rs199893521 | snp | A/G | 1.65954e-05 | 0.00288053 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84772683 | ACTTGGAAATTAGTA[A/G]AGGTAATGCATACAT | 9100 |
| rs199897026 | in-del | -/TG | | | intron-variant | USP10 | GRCh38.p7 | 16:84765260 | ACAGTTACCCTTGTG[-/TG]TGTGTGTGTGCACAT | 9100 |
| rs199903066 | in-del | -/G | 0.00478085 | 0.0486577 | intron-variant | USP10 | GRCh38.p7 | 16:84731785 | TAGCTCTTTTTTTTT[-/G]TGTGATAGTCTGTGC | 9100 |
| rs199955512 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84754990 | TAGACTTTGTCCCAG[A/G]AAAAAAAAAAAAGGA | 9100 |
| rs199959868 | snp | C/G | 4.96808e-05 | 0.00498377 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84772565 | AGTCGAAGAGTGACT[C/G]TGGAAAAACTCCCTC | 9100 |
| rs199963685 | snp | A/G/T | 0.00015005 | 0.00866049 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744877 | TTCTAATGTGGAGGC[A/G/T]GAAGTTTTGGAAAAT | 9100 |
| rs200061898 | in-del | -/GTGTGTGT | | | intron-variant | USP10 | GRCh38.p7 | 16:84757403 | ATGAGAGGGGTGGGG[-/GTGTGTGT]GTGTGTGTGTGTGTG | 9100 |
| rs200078985 | snp | C/T | 0.495535 | 0.0470365 | intron-variant | USP10 | GRCh38.p7 | 16:84732459 | CTTTTTTTTTTTTTT[C/T]TTTTTGAGATGGAGT | 9100 |
| rs200099821 | snp | A/G | 0.000299755 | 0.0122388 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744869 | GATGGAAGTTCTAAT[A/G]TGGAGGCGGAAGTTT | 9100 |
| rs200146033 | snp | C/G | 9.95785e-05 | 0.00705545 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84763076 | AAGAAGCTTCTCTCA[C/G]CAAGTAATGAAAGTA | 9100 |
| rs200274721 | in-del | -/ACTC | 0.00755907 | 0.0610114 | intron-variant | USP10 | GRCh38.p7 | 16:84711025 | CCCTCTGAGTGTGAT[-/ACTC]ACTTATTTTAGCGCC | 9100 |
| rs200324193 | snp | C/T | 0.000231957 | 0.0107668 | intron-variant | USP10 | GRCh38.p7 | 16:84758817 | AATGCTGTATCCTTC[C/T]TGGACGCCGTCCGCA | 9100 |
| rs200340615 | in-del | -/GC | | | intron-variant | USP10 | GRCh38.p7 | 16:84735270 | AAGGGGATTTTGTAT[-/GC]TTTTTCCCACATCAC | 9100 |
| rs200436268 | snp | C/T | 3.31505e-05 | 0.00407113 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764187 | GAACAAGTGGGCCCC[C/T]GGAACAAGACTTCCG | 9100 |
| rs200480434 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84720601 | TTTTTTTTTTTTTTG[A/T]GATGGAGCCTCGCTG | 9100 |
| rs200546125 | snp | A/G | | | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84760257 | CCTGACAGTTAACAA[A/G]TCAAGCCTGTCTGAA | 9100 |
| rs200546167 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84775898 | CGTCATCTTTTATGC[A/C]TCTGAGTCTTTACCT | 9100 |
| rs200571986 | snp | A/G | 0.000157561 | 0.00887444 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745639 | AGAAGGGCTTGTTCC[A/G]GTTTCAGAGGATCCT | 9100 |
| rs200642316 | in-del | -/AA | 0.457504 | 0.139435 | intron-variant | USP10 | GRCh38.p7 | 16:84755796 | GAGTGAGACTGTCTC[-/AA]AAAAAAAAAAAAAAA | 9100 |
| rs200720877 | in-del | -/TT | 0.00795532 | 0.062565 | intron-variant | USP10 | GRCh38.p7 | 16:84765255 | CCATCACAGTTACCC[-/TT]GTGTGTGTGTGTGTG | 9100 |
| rs200755558 | snp | C/T | 0.00058085 | 0.017032 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744820 | AAGCTATGGCTCCAT[C/T]GACTGCCAGTACCCA | 9100 |
| rs200790580 | snp | G/T | 0.0100718 | 0.0702458 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745655 | GTTTCAGAGGATCCT[G/T]TAGCCATAAAGATTG | 9100 |
| rs200798347 | in-del | -/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84758479 | TTCCCTAATTCTGTT[-/C]CCCCCAGGAAGATTA | 9100 |
| rs200805483 | in-del | -/ATGAC | | | intron-variant | USP10 | GRCh38.p7 | 16:84753467 | TGTATTGAGCTGGCC[-/ATGAC]GTCATGCCGGGAGTG | 9100 |
| rs200833553 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84700719 | AAGGACCGTACTTTC[A/G]CTTGCGTTTGAGTGA | 9100 |
| rs200845753 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | USP10 | GRCh38.p7 | 16:84746447 | GCCTTAGGCTGGTGG[G/T]GCAGCCTATTACTCC | 9100 |
| rs200971353 | snp | C/G | 4.97599e-05 | 0.00498773 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744795 | CCCCTGATGGTATCA[C/G]TAAAGAAGCAAGCTA | 9100 |
| rs200981341 | in-del | -/A | 0.0142736 | 0.0832652 | intron-variant | USP10 | GRCh38.p7 | 16:84767776 | AGCAGAATTATTATT[-/A]TTTTTTTTAATTTAT | 9100 |
| rs201021360 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84702917 | AGAATCGCTTGAACC[C/G]GGGAGGCGGAGGTTG | 9100 |
| rs201068388 | snp | A/C/G | 6.6291e-05 | 0.00575683 | missense, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779017 | ATCAACCAGTACCAG[A/C/G]TGGTGAAACCAACTG | 9100 |
| rs201080577 | snp | A/G | 1.6593e-05 | 0.00288031 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764144 | AGAAGAGCAGGAAGA[A/G]CAAGGTGAAGGAAGC | 9100 |
| rs201088868 | in-del | -/T | 0.10457 | 0.203575 | intron-variant | USP10 | GRCh38.p7 | 16:84731117 | CTGAGTAGCTGGGAC[-/T]TACAGGTGCATGCCA | 9100 |
| rs201116534 | in-del | -/TTC | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84734251 | CAGTGCATGGGAGTT[-/TTC]TTGCTCGTATTAAAA | 9100 |
| rs201186851 | snp | A/G/T | 0.000534436 | 0.0163388 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745424 | ATAGACTTGGACCCA[A/G/T]CCAAACCCGAGAGTG | 9100 |
| rs201206784 | in-del | -/TTTGT | 0.0221141 | 0.102801 | intron-variant | USP10 | GRCh38.p7 | 16:84721692 | GCCACCAAGTCTGGC[-/TTTGT]TTTGTTTTGTTTTGT | 9100 |
| rs201313659 | snp | A/G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84764937 | AGAGAGAGAGAAAAA[A/G/T]AAATATATATATATA | 9100 |
| rs201317349 | snp | C/G | 3.4478e-05 | 0.00415184 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745175 | CCTTTCCCCGGAGCA[C/G]TCGGCAGTGACACCA | 9100 |
| rs201325247 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84746174 | TGAAGAGAAAAAAAA[-/T]GTTAAGGGTTCAGCC | 9100 |
| rs201350427 | in-del | -/C | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698600 | TTTCTTTCTTTCTTT[-/C]TTTTTTTTTTTTTGA | 9100 |
| rs201361121 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84748959 | TTGGTTAGGTCAGTT[A/C]TGAAGATGTTTTAAT | 9100 |
| rs201418927 | snp | A/G | 1.662e-05 | 0.00288266 | intron-variant | USP10 | GRCh38.p7 | 16:84758678 | TGTTCTTCACTAGAT[A/G]TCATCAATTTCTGAA | 9100 |
| rs201465777 | in-del | -/A | 0.382689 | 0.211881 | intron-variant | USP10 | GRCh38.p7 | 16:84762691 | ATGAGACTTTGTCTC[-/A]AAAAAAAAAAAAAGT | 9100 |
| rs201495408 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84732444 | TGACTTCTTCTTCTT[C/T]TTTTTTTTTTTTTTC | 9100 |
| rs201523258 | snp | A/G | 0.0029955 | 0.0385847 | intron-variant | USP10 | GRCh38.p7 | 16:84732145 | TGTGCATTCTTACCA[A/G]GAGGGTATTACATTT | 9100 |
| rs201540653 | in-del | -/GTCGC | | | intron-variant | USP10 | GRCh38.p7 | 16:84737740 | TCTGAAGCTGGCAGT[-/GTCGC]CTGGCTTCCTCATCT | 9100 |
| rs201565734 | in-del | -/C | 0.00348431 | 0.0415934 | intron-variant | USP10 | GRCh38.p7 | 16:84732446 | CTTCTTCTTCTTCTT[-/C]TTTTTTTTTTTTCTT | 9100 |
| rs201597070 | snp | A/G | 0.000480571 | 0.0154937 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745289 | TCAAGGACAGCTGGG[A/G]CTCAGCCCTGCGTTG | 9100 |
| rs201614220 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84715797 | GTTTTGAGGACGTGG[C/T]TTCTTTTCATTTTTT | 9100 |
| rs201635042 | snp | A/G | 0.000281678 | 0.0118642 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84759896 | CCATGTTTAGTGTTC[A/G]GCTAATGAATGAGTT | 9100 |
| rs201716776 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84760156 | TAGGAAAACCTGTGT[C/G]CTCTTTCCATTGCAG | 9100 |
| rs201719300 | snp | A/G | 0.000215898 | 0.0103876 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84763083 | TTCTCTCACCAAGTA[A/G]TGAAAGTAGGTTATG | 9100 |
| rs201725370 | snp | C/T | 6.86165e-05 | 0.00585692 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779106 | TGCGCTGTGTGTGCG[C/T]CCAGTGCCCGCTTCG | 9100 |
| rs201747945 | in-del | -/A/TA | | | intron-variant | USP10 | GRCh38.p7 | 16:84767789 | TATTTTTTTTAATTT[-/A/TA]ATTTTTTTATTGATA | 9100 |
| rs201757710 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84765758 | GAGAGTGTGAAGGGA[C/G]GTCTTTTTTACACAG | 9100 |
| rs201836670 | in-del | -/CA | | | intron-variant | USP10 | GRCh38.p7 | 16:84706913 | TTGGAGAAGGAGAAA[-/CA]TATTTATTACGAGAT | 9100 |
| rs201868210 | snp | C/T | 0.0039921 | 0.0444985 | intron-variant | USP10 | GRCh38.p7 | 16:84759861 | TATTGTTTAAAACTG[C/T]ACTATTTAACATTTT | 9100 |
| rs201884056 | in-del | -/GGT | | | intron-variant | USP10 | GRCh38.p7 | 16:84757396 | GGAGGGAATGAGAGG[-/GGT]GGGGGTGTGTGTGTG | 9100 |
| rs201942996 | snp | C/T | 4.99077e-05 | 0.00499513 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745660 | AGAGGATCCTGTAGC[C/T]ATAAAGATTGCAGGT | 9100 |
| rs201988751 | in-del | -/A | 0.4444 | 0.15719 | intron-variant | USP10 | GRCh38.p7 | 16:84714935 | ATTATTATTATTATT[-/A]TTTTTTTTTTTTGAG | 9100 |
| rs202007733 | in-del | -/T | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698596 | TTCTTTCTTTCTTTC[-/T]TTTCTTTTTTTTTTT | 9100 |
| rs202025437 | snp | C/G | 1.65655e-05 | 0.00287793 | missense, intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84740333 | TACAGTGGAACAGTT[C/G]TGTGTGGCACACAGG | 9100 |
| rs202050984 | snp | A/G | 0.00075171 | 0.0193724 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744927 | TTGGACAAAGGGAGC[A/G]TAAAAAGAAGAAAAA | 9100 |
| rs202101090 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84706875 | TCAAGACCTGAAGTA[G/T]GCTTTCTGGGTAGAT | 9100 |
| rs202133199 | snp | C/T | 0.00019887 | 0.00996972 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84775170 | TCCAGAACTGCTTTC[C/T]CCAGGGGTTAAAAAT | 9100 |
| rs202133795 | in-del | -/A | | | intron-variant | USP10 | GRCh38.p7 | 16:84734897 | TTCATTGGGAACTCG[-/A]GCCCTTAGCTGTCCT | 9100 |
| rs202153570 | in-del | -/C | 0.00696856 | 0.058615 | intron-variant | USP10 | GRCh38.p7 | 16:84732444 | TGACTTCTTCTTCTT[-/C]TTTTTTTTTTTTTTC | 9100 |
| rs202165217 | snp | C/G | 0.00399193 | 0.0444975 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745232 | CCCGGGGCTGATTTT[C/G]GTCAGTCCTGCTTCC | 9100 |
| rs202205096 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84712558 | CTTATGGTTGTTTTT[A/C]GTGTTTCTATAATAG | 9100 |
| rs202218800 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84734036 | TATTTTCCTGTCGAG[A/G]GCCATTTAGGTCTCT | 9100 |
| rs202224730 | in-del | -/TC | 0.0009298 | 0.0215415 | intron-variant | USP10 | GRCh38.p7 | 16:84732443 | ATGACTTCTTCTTCT[-/TC]TTTTTTTTTTTTTTC | 9100 |
| rs367543342 | snp | A/G | 3.32552e-05 | 0.00407756 | missense, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779057 | CAGCCTACCTCCTGT[A/G]TTACCGCCGAGTGGA | 9100 |
| rs367545642 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84776147 | GGATCCCTGTTTTAT[A/G]AAAGAATAAACCAGA | 9100 |
| rs367550397 | snp | C/G | 0.000167986 | 0.00916323 | intron-variant | USP10 | GRCh38.p7 | 16:84760163 | ACCTGTGTCCTCTTT[C/G]CATTGCAGCTCTTGG | 9100 |
| rs367561903 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84754486 | ACGTCCCAAGGGCCC[A/G]TACGTATGTTCTGCT | 9100 |
| rs367562963 | snp | A/G | 1.66261e-05 | 0.00288319 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764235 | TTTGTTCAGACTCCA[A/G]TCACCGGCATTTTTG | 9100 |
| rs367563387 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84766503 | CAGCCCAGCAGCCTG[C/G]TTTAGGATTGTGAGG | 9100 |
| rs367579382 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP10 | GRCh38.p7 | 16:84771755 | AGCCTGTAATCCCAG[C/T]TACTCAGGAGGCTGA | 9100 |
| rs367597644 | in-del | -/CTCTTTAGTAAAAG | | | intron-variant | USP10 | GRCh38.p7 | 16:84759828 | ACTTAGCCATCAAAG[-/CTCTTTAGTAAAAG]TATATATTGTTTAAA | 9100 |
| rs367629949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84771919 | GTGGTACTAAGTTAG[C/T]TTTTTAATTTTTATG | 9100 |
| rs367646533 | snp | C/G/T | 0.00438476 | 0.0466401 | intron-variant | USP10 | GRCh38.p7 | 16:84766094 | AAAGAAAGAGCACCC[C/G/T]TTTTGAGGCATCAAG | 9100 |
| rs367648543 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84754826 | CCATGCAGATTATTC[G/T]GGGCCCCTAACTCAG | 9100 |
| rs367677043 | in-del | -/T | | | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719201 | GACATCTGGATGTTG[-/T]TCATCAACTTTATAT | 9100 |
| rs367677668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719663 | GATTGGGTGGAAAAC[A/G]TCTCTTCTAGTGTAT | 9100 |
| rs367693313 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84729013 | ATTTTGGCTGGGCTG[A/G]TCTTGAACTCCTGAA | 9100 |
| rs367732559 | snp | A/C/G | 0.00597247 | 0.0543191 | intron-variant | USP10 | GRCh38.p7 | 16:84774165 | TGAGGCAGGAGAATC[A/C/G]CTTGAACCTGGGAAG | 9100 |
| rs367749783 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84764434 | TCCCTTGTCAGCCCC[C/T]GTGGCTTATTCTCTC | 9100 |
| rs367802303 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84726811 | AAGCCCTTGTACTTT[C/G]CTCCCCCGAATCGCA | 9100 |
| rs367843621 | snp | A/G | 0.000163987 | 0.00905353 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84763078 | GAAGCTTCTCTCACC[A/G]AGTAATGAAAGTAGG | 9100 |
| rs367852987 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84775384 | TGAGAGTTTTACCTG[A/G]AACTCTGCGTAGATG | 9100 |
| rs367933899 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84752105 | TGAAATTTCAGTTCA[C/G]CCTTTTCATGTGAGT | 9100 |
| rs367936239 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84741741 | GACAGGCCTGCTTTT[C/T]TCTGCAGCCTTTCTG | 9100 |
| rs367994867 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84722461 | CGTATATTCTATTCT[A/G]TAAGAAACTGCAAGG | 9100 |
| rs368012900 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84712253 | GCTGTGTACAGAGGC[C/G]CTTGTGGTCCTGTCC | 9100 |
| rs368054549 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84738688 | TAAGTGCAGCTGTCA[A/G]CTCCTGAAGGTGTTG | 9100 |
| rs368059810 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84701530 | AAATCCTAATTAACT[A/G]GCTTATTAGAATTGG | 9100 |
| rs368064649 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | USP10 | GRCh38.p7 | 16:84715767 | AAGTTGGTTTAATTC[A/G]GCCGTTTAGTTACAG | 9100 |
| rs368123897 | in-del | -/TCT | 0.0134861 | 0.0810011 | intron-variant | USP10 | GRCh38.p7 | 16:84728797 | TTTATAAGCAGCACC[-/TCT]TCTTTTTTCTTTTTT | 9100 |
| rs368129911 | snp | C/T | 1.65974e-05 | 0.0028807 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744811 | TAAAGAAGCAAGCTA[C/T]GGCTCCATCGACTGC | 9100 |
| rs368152921 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84721034 | GAGTAGCCGGGAGTA[C/T]AGGTGCCCGCCACCA | 9100 |
| rs368184409 | snp | C/G/T | 1.66532e-05 | 0.00288554 | intron-variant | USP10 | GRCh38.p7 | 16:84733548 | GTGGGTAGATACAAT[C/G/T]AATAGTTATGTTTCT | 9100 |
| rs368191606 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84757915 | TCAATTGTAAAGAAC[A/G]TGCTAAGTGTAGAAG | 9100 |
| rs368194901 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84769032 | AGCTATTTTGTACTC[G/T]GCAGCAGAGAGTGTC | 9100 |
| rs368252487 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84778718 | GTTTTTATTATGGAT[G/T]GCTTGCGTGTTTGAG | 9100 |
| rs368267475 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84723019 | GGAGGGACCAAGAAA[C/T]ACAGGATGCATGCCT | 9100 |
| rs368267983 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718396 | GGAGCTGGGACTGCA[A/G]GTGTGGGCCACTGTG | 9100 |
| rs368276487 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84769059 | TGTCTTCTCTGTTAT[A/C]TATCTTAGGTTGTGG | 9100 |
| rs368340915 | snp | A/C | 0.000163986 | 0.00905352 | intron-variant | USP10 | GRCh38.p7 | 16:84740381 | GATGGTAAGCTAGTT[A/C]TCTCCTTATTTCCCT | 9100 |
| rs368341828 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84717026 | TAGCAGTGCTTCTCA[A/T]ACTTAAAAGTCCGTT | 9100 |
| rs368348227 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84714004 | CTGCTAGAGCCTTTT[A/C]GCCTGAAAAGTTCTG | 9100 |
| rs368359341 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84756113 | CCCCATCTCCCAACA[C/G]CCCTTCAGCTTAGCC | 9100 |
| rs368367922 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84724617 | AGTGAGGGAACAAAA[C/G]TTCTCTTCCTCCTTC | 9100 |
| rs368382004 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84771610 | GTGGTGGCTCACGCC[G/T]GTAATCTCAGCACTT | 9100 |
| rs368384048 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84755376 | CCTAGCTCCTTGCAC[C/G]CATGATCCTGTCTCC | 9100 |
| rs368412158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84726694 | GAGTTTTGAAAGCCC[A/G]GGATGGAGGCCGGAT | 9100 |
| rs368436369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84753962 | GTTGAGGGGAGAAAG[C/T]AAGGAGGGGAGGCCT | 9100 |
| rs368552280 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718529 | TTTGGGAGGCCAAGG[C/T]GGGTGGATCACCTGT | 9100 |
| rs368574309 | snp | A/C/G | 6.62739e-05 | 0.00575614 | missense, nc-transcript-variant, intron-variant | USP10 | GRCh38.p7 | 16:84759430 | TTCCTCTGTATTCCA[A/C/G]AGTGCAAAGGCCTTG | 9100 |
| rs368587353 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84760909 | GAAATGATGCTTAGG[G/T]AAATGTATTCAGAGA | 9100 |
| rs368647564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84729151 | ATGCTTCTTCATTGT[A/G]GTGCTTTGAATGATG | 9100 |
| rs368677913 | snp | G/T | 0.000136207 | 0.00825137 | intron-variant | USP10 | GRCh38.p7 | 16:84745687 | AGGTATAGTTGAAAA[G/T]ATACAAATCTAGAGT | 9100 |
| rs368734058 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84740860 | CCTCCTGGTCTGTTA[A/C]TTTTTTGGGTCTCCA | 9100 |
| rs368734787 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84774482 | GTTTTGTTTTTTTTT[-/T]GTTTGTTTGTTTTTT | 9100 |
| rs368747403 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84769152 | AGCATTCCTGCAAAG[C/T]GATATTTGAATAATG | 9100 |
| rs368766973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84760599 | CTTAACCACTGCACT[A/G]TATGCCACTGGGGTA | 9100 |
| rs368768028 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84769515 | TCTGGCGGTGGACCT[C/T]GTGGAAGAGAGAGAG | 9100 |
| rs368823919 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84740430 | CGTGCTGGGTGGGCA[A/G]GCTACCTGTAAACAT | 9100 |
| rs368825061 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84755740 | GAGGCGGAGGTTGGA[A/G]TGAGCTAGGATGGTG | 9100 |
| rs368828194 | snp | C/G/T | 5.73744e-05 | 0.00535579 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745576 | GGAAACTAAGTATTC[C/G/T]CCTCCCGCCATATCT | 9100 |
| rs368859116 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84721389 | ATTACAACTGTGGCC[A/G]TTGGTCTTCAAGAGC | 9100 |
| rs368873055 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84774952 | CTGTTTCTTTAGTGA[A/G]CTGGCTGCACATTTT | 9100 |
| rs368880191 | snp | A/T | 1.65902e-05 | 0.00288008 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84763073 | CTAAAGAAGCTTCTC[A/T]CACCAAGTAATGAAA | 9100 |
| rs368919556 | snp | A/G | 0.00219854 | 0.0330823 | intron-variant | USP10 | GRCh38.p7 | 16:84760300 | TTCTCTGTTGTCACT[A/G]GTATCAAGTGTTGCC | 9100 |
| rs368921258 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84777172 | TTTCAGGCGGTTCTC[A/C]GCGCTCCTGTCAGGG | 9100 |
| rs368976904 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84734663 | AATTGATTTTTTTTT[A/C]CTTATAGTTTGTGGA | 9100 |
| rs368992379 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84710829 | GTGAGCAGGTCCCCA[C/G]GCCGTCTGAGCCAGG | 9100 |
| rs369035180 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84732150 | ATTCTTACCAGGAGG[G/T]TATTACATTTAGTGG | 9100 |
| rs369049821 | snp | C/T | 8.81733e-05 | 0.00663919 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779120 | GCCCAGTGCCCGCTT[C/T]GTAGGACACCACCTC | 9100 |
| rs369053957 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84708227 | GGTCGAGGTGGGTGG[A/G]TCACCTGAGGTCAGG | 9100 |
| rs369054433 | snp | A/G | 1.65999e-05 | 0.00288091 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744818 | GCAAGCTATGGCTCC[A/G]TCGACTGCCAGTACC | 9100 |
| rs369059618 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84769414 | GCAGACTTGCATCTC[A/C]TGGGTGATTTTGTTT | 9100 |
| rs369070022 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84705502 | TCCCAAAGTGCTGGG[A/G]TTATAGGCGTGAGCC | 9100 |
| rs369133987 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | USP10 | GRCh38.p7 | 16:84751006 | CCTGTCCGTGTTTAT[G/T]TAAGTGTAAATGAAC | 9100 |
| rs369137532 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84723859 | CATTCCCCAGAATGA[C/G]ATTGAGCCCCCTTGC | 9100 |
| rs369156436 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84770306 | TAAGGAGCAAATTAC[A/G]TATTTTCTTGAATGT | 9100 |
| rs369176775 | snp | C/T | 5.07292e-05 | 0.00503607 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84760201 | ATCGTGAGGGATATT[C/T]GCCCTGGAGCTGCCT | 9100 |
| rs369189256 | in-del | -/CA | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84709561 | AGTGAAGAATAGACT[-/CA]CGGGGTCGCAGTGGC | 9100 |
| rs369191395 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84711833 | CAAGTGATTCTCTGG[C/T]CTCAGCCTCCTGAGT | 9100 |
| rs369192171 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84758865 | CTGTCCCTCCTTTGG[C/G]TGCATGTGACTTAGC | 9100 |
| rs369229466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84720198 | GTAGCTAGGTTCTTT[C/T]TTCATGGATGTCCTT | 9100 |
| rs369278575 | snp | C/T | 0.000182362 | 0.00954714 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744726 | ACAGTATTTCAAGCA[C/T]ACTGAACCCTCAGGC | 9100 |
| rs369314047 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84758056 | AGCTGTTTTAATACA[A/C]AGAAAGAGTGATGTC | 9100 |
| rs369352655 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717316 | ACCCAAAAAAGATTA[A/G]GAATCCTCCCTTTTA | 9100 |
| rs369367247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84743040 | CCTTCCGCCCCAGGC[A/G]CACCCGTTTCAATCT | 9100 |
| rs369374222 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84764943 | AGAGAAAAAAAAATA[A/T]ATATATATATATTAG | 9100 |
| rs369382426 | snp | A/G | 0.000707564 | 0.0187958 | utr-variant-5-prime, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84700041 | GGCGGCGGCGGGGGA[A/G]GCAGCGTGAGCAGCC | 9100 |
| rs369383543 | snp | A/G | 3.75016e-05 | 0.00433006 | intron-variant | USP10 | GRCh38.p7 | 16:84768402 | CTACTAAGGTGCTCT[A/G]GTTTGGTGGAAAGAA | 9100 |
| rs369404643 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84711128 | GTCGTGTCTTCAGAA[A/C]GAGATTTCAGTTTGG | 9100 |
| rs369419326 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84714731 | GCACATTATTGTAAA[C/G]TGGAAGATGAACGTC | 9100 |
| rs369429954 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84726216 | TGCTGCAGCGCCCCC[-/T]AGTGCCGTGCTGTAC | 9100 |
| rs369441184 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84742341 | CCTGCATCCAGAAGA[A/G]TCCTTTTTCTAAAGC | 9100 |
| rs369445520 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84748366 | CGGAATGCAGTGGCG[C/T]AATCTCGGCTCACTG | 9100 |
| rs369455508 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84724689 | TTGCAGTTGGCTTGC[A/C/G]CTGTAATAAAACTGT | 9100 |
| rs369470393 | snp | C/T | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698003 | ACAGGTGTGAGCCAC[C/T]GCACCGAGCCAGAGA | 9100 |
| rs369471456 | snp | A/G | | | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84716515 | TTCATTCACAGAGAC[A/G]TAGGTAAATGAGAAT | 9100 |
| rs369486044 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84752613 | TTGGAAGTGGTATTA[A/G]TTCTGGCTTGTCCGT | 9100 |
| rs369506104 | snp | A/G | 6.63625e-05 | 0.00575993 | intron-variant | USP10 | GRCh38.p7 | 16:84759865 | GTTTAAAACTGCACT[A/G]TTTAACATTTTTTCC | 9100 |
| rs369558030 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84776318 | GCCTAGCGGTGGGGG[C/G]CCAGGGGTGAGGGCC | 9100 |
| rs369562546 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84768089 | GGTCTTTTGAAAGTG[A/T]TATTGAATAATCTTA | 9100 |
| rs369576890 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84775761 | ACCCCCTGTTCCCTC[A/G]TGGGTGGACCTTGAG | 9100 |
| rs369598290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84721790 | GCAACCTCCGCCTCC[C/T]GGGTTCAAGCAATTC | 9100 |
| rs369600396 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84755226 | ATGAACATGTTCAAG[C/G]CCCGTCTCACCCACC | 9100 |
| rs369604243 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84702873 | TGAAGCTCGCCTGTA[A/G]TCCCAGGTACTTGGG | 9100 |
| rs369646101 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84774674 | ACGTGGTTTCACTGT[A/G]TTAGCCAGGATGGTC | 9100 |
| rs369647790 | snp | A/G | 8.15805e-05 | 0.0063862 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84760255 | CTCCTGACAGTTAAC[A/G]AGTCAAGCCTGTCTG | 9100 |
| rs369649364 | snp | A/C/G | 0.0185938 | 0.0946107 | intron-variant | USP10 | GRCh38.p7 | 16:84726801 | GAAATGCCTGAAGCC[A/C/G]TTGTACTTTGCTCCC | 9100 |
| rs369652686 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84752540 | GGAATAACATTGTAA[A/G]TGAAAATGTTGATGT | 9100 |
| rs369659891 | snp | A/G | 6.63493e-05 | 0.00575936 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744789 | AAATAACCCCTGATG[A/G]TATCACTAAAGAAGC | 9100 |
| rs369660018 | snp | C/G | 1.72359e-05 | 0.00293558 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779110 | CTGTGTGTGCGCCCA[C/G]TGCCCGCTTCGTAGG | 9100 |
| rs369667944 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84706834 | CGTGAGCCACCGCGC[C/T]GGGCCAAGACTATAT | 9100 |
| rs369709272 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84727408 | AGTCAAACATAAGGA[A/G]AGGGTAAAGGTTTTC | 9100 |
| rs369767779 | snp | A/C | 1.65701e-05 | 0.00287833 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84759917 | TGAATGAGTTCACTA[A/C]TATGCCAGTACCTCC | 9100 |
| rs369776943 | snp | A/G | 9.95983e-05 | 0.00705615 | missense, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84733469 | GCCCTGATGAATTCA[A/G]TCAATTCTTTGTGAC | 9100 |
| rs369783105 | snp | C/T | 0.000313951 | 0.0125251 | intron-variant | USP10 | GRCh38.p7 | 16:84778859 | ATTCGTGTGCAGTGC[C/T]GTTCTCACTCTGCTG | 9100 |
| rs369792761 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84734033 | ACATATTTTCCTGTC[G/T]AGGGCCATTTAGGTC | 9100 |
| rs369804105 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84710169 | CAGCTACTTGAGAGG[C/T]TTAGGCAAGAGAATC | 9100 |
| rs369807640 | in-del | -/CA | | | intron-variant | USP10 | GRCh38.p7 | 16:84771511 | AAAAAAACAAACAAA[-/CA]AAAAAACCCACCTAA | 9100 |
| rs369814037 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84730193 | TTTTCTTGTTGATCT[C/T]TCCAGTGTCTCTTTA | 9100 |
| rs369832457 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84703319 | GTGATTATTGATGTC[A/G]TTTATAGTGAAATCT | 9100 |
| rs369862528 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84722421 | GGACATAGGTTTTCA[C/T]TTCTTGTGGGTAAAA | 9100 |
| rs369931502 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84735203 | GCCCGGGTGGTGTGT[A/G]TGTGTGTGTGTGTGT | 9100 |
| rs369948332 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84741475 | CATGTTGAACCAGTG[C/T]TTACAAATGCCCCAT | 9100 |
| rs370017414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84720823 | TCCTGACCTCATGAT[C/T]TGCCCACCTCGACGT | 9100 |
| rs370037155 | snp | A/G | 6.62438e-05 | 0.00575478 | missense, nc-transcript-variant, intron-variant | USP10 | GRCh38.p7 | 16:84758779 | CCCGTGGGCTGATCA[A/G]TAAAGGGAACTGGTG | 9100 |
| rs370038448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84770550 | GGCCAAGGCGGGTGG[A/G]TCACGAGGTCAGGAG | 9100 |
| rs370050970 | snp | A/C/G/T | 0.000126469 | 0.00795122 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764092 | CCTTTTCAGAACTTA[A/C/G/T]GATTTCCAACGGCCC | 9100 |
| rs370051516 | snp | A/G | 3.31301e-05 | 0.00406989 | intron-variant | USP10 | GRCh38.p7 | 16:84772532 | GTCCTGGTGTGCTTT[A/G]TGTCTTAGGTTGAGA | 9100 |
| rs370107084 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84702142 | CCCACTGCAACCTCT[-/T]GCCTCCCGGGTTCAA | 9100 |
| rs370111116 | snp | C/G | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698672 | ACGATCTCGGCTCAC[C/G]GCAACCTCCGTCTCC | 9100 |
| rs370154468 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84721236 | GTAGCACTGGGAGGT[A/C]TTTGGACCAAGGAAT | 9100 |
| rs370158526 | snp | C/G | 5.01299e-05 | 0.00500624 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745426 | AGACTTGGACCCAAC[C/G]AAACCCGAGAGTGCA | 9100 |
| rs370164533 | snp | C/T | 9.97987e-05 | 0.00706324 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764240 | TCAGACTCCAATCAC[C/T]GGCATTTTTGGTGGA | 9100 |
| rs370168248 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84747246 | GCTGTTTGGTTTAGG[A/C]TTTCTGTAATACTTT | 9100 |
| rs370198338 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84750914 | GTTTATATGATTTTT[C/T]ACAGTGGTTTTATAC | 9100 |
| rs370205909 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84738514 | ACTGCCCTTATAGAC[C/T]CACCTCTCTGCTCCA | 9100 |
| rs370212053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84701978 | ATTTGGCTCTTGTTG[C/T]CCAGGCTGGAGTGCT | 9100 |
| rs370212759 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84752211 | ACATTGTTCTAGGCA[G/T]CCCCACCAACTCCTG | 9100 |
| rs370214162 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84725147 | ATTTTAGAACATTTC[A/G]TCATCCCCAAAAGAA | 9100 |
| rs370214373 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84770668 | TCCCAGCTACTCAGG[A/G]GGCTGAGGCAGGAGA | 9100 |
| rs370283774 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84768547 | CCCAAGGGCCTCTTT[G/T]AGCTCTAAATCATAT | 9100 |
| rs370285937 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84778215 | CCACCACAGCTCCAC[A/G]CTCAAGCAACCGTGG | 9100 |
| rs370311594 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84707986 | GGGAGGTTGAGGTGG[A/G]AGGATCGCTTGAACC | 9100 |
| rs370321855 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84740481 | ATTTCTTTGTAGCTT[A/G]AAGTTTTTGCTGTAA | 9100 |
| rs370329666 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84759097 | CCACTTACAACTGGA[A/T]ATTTGGTTTTAACTG | 9100 |
| rs370347352 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84746448 | CCTTAGGCTGGTGGT[A/G]CAGCCTATTACTCCC | 9100 |
| rs370351772 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84773463 | CCTCCTTCCATATAG[A/G]TGACCCAGGAACTGT | 9100 |
| rs370353711 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84710519 | CAGTGGTAATTGGAT[A/G]GAGTAGTTAGGGAAG | 9100 |
| rs370359854 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84734049 | AGGGCCATTTAGGTC[A/T]CTAGTTCAGCCGTTA | 9100 |
| rs370370137 | in-del | -/CT | | | intron-variant | USP10 | GRCh38.p7 | 16:84752721 | ACTGCTTTTGCACCC[-/CT]GTTTTTTTCACTGCG | 9100 |
| rs370373929 | in-del | -/CATGA | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84753466 | CTGTATTGAGCTGGC[-/CATGA]CGTCATGCCGGGAGT | 9100 |
| rs370383030 | in-del | -/AAAAAAAAAATATAT/AAAAAAATATAT/TATAT | | | intron-variant | USP10 | GRCh38.p7 | 16:84764939 | GAGAGAGAAAAAAAA[lengthTooLong]ATATATATATATATA | 9100 |
| rs370404574 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84757295 | CACAGAATCTGTAAT[A/G]TTTTACTTTCTACAG | 9100 |
| rs370416210 | snp | C/T | 0.000241237 | 0.01098 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84760230 | CTTTGAGCCCACATA[C/T]ATTTACAGACTCCTG | 9100 |
| rs370441838 | snp | C/T | 3.31395e-05 | 0.00407046 | intron-variant | USP10 | GRCh38.p7 | 16:84759976 | GTTTTGTTGATGCTA[C/T]TACATATTGGGAGTT | 9100 |
| rs370459581 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84770085 | TGCACTCCAGCCTGT[-/T]GCGATAGTGAAACCG | 9100 |
| rs370488584 | snp | A/G/T | 0.000464235 | 0.015229 | intron-variant | USP10 | GRCh38.p7 | 16:84758835 | GACGCCGTCCGCAAG[A/G/T]CCAGCTTGTTGCAGC | 9100 |
| rs370525384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84728439 | CTGCCTCCCCGGTTC[A/G]AGCGATTCCCCTGCC | 9100 |
| rs370553469 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84722904 | ATGATAATTTTTTGT[C/T]CCTAGGAACATGAGT | 9100 |
| rs370572170 | snp | A/C | 5.06872e-05 | 0.00503399 | intron-variant | USP10 | GRCh38.p7 | 16:84762952 | GCCTTTGACAGTGAT[A/C]AGTTCACAGTAACGT | 9100 |
| rs370575743 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84710125 | AAATACAAAAATTAG[C/G]CGGGCGTGGTGGCGC | 9100 |
| rs370590178 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718039 | AACAATGATGAGAGA[C/G]AGATTGGGAGATTAC | 9100 |
| rs370617796 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84703238 | TTGTCACTGAGGGGA[C/G]CGGTTAAATTATTTG | 9100 |
| rs370618320 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84768731 | AGATTAGTTAGGATG[G/T]CAGAGAGATTCCAGA | 9100 |
| rs370651418 | snp | A/C | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698344 | AATGCATCTCCTCAC[A/C]ATAAGGACATTCTCT | 9100 |
| rs370675131 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84720453 | TGGTCCGAGAAGCTC[A/G]GCAGTAATAAAGGTT | 9100 |
| rs370711954 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84738781 | GCGTTACTAGCAGAG[A/G]GAAGCTTTTATTGCT | 9100 |
| rs370760094 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84719072 | GCTGGGATTACAGGC[A/C]TGAGCCACCGCGCCC | 9100 |
| rs370762551 | snp | C/G | 0.00119737 | 0.0244387 | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780352 | ACGTGCAAGGGTGCC[C/G]GTGCCCCGGCTTCTG | 9100 |
| rs370773402 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84743840 | AAGAGATATTTAAAA[A/G]TTCACAATTCTAACT | 9100 |
| rs370819796 | snp | A/G | 0.000232284 | 0.0107744 | intron-variant | USP10 | GRCh38.p7 | 16:84772498 | GTGTTAGCTGTTGCA[A/G]GTAAGACAGGGACGG | 9100 |
| rs370823182 | snp | A/G | 0.000165986 | 0.00910854 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744957 | AGCGGCCACCTGGAT[A/G]TTACAGCTATTTGAA | 9100 |
| rs370825039 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84709139 | AGGCATTGTTTCTCT[C/T]GCGGAGGAGTTTATG | 9100 |
| rs370846637 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84740155 | AAGATGATTTAGATT[A/G]CACTGACTCTTCATG | 9100 |
| rs370847972 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84774164 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCTGGGAA | 9100 |
| rs370866289 | snp | C/G/T | 1.65737e-05 | 0.00287864 | missense, synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764192 | AGTGGGCCCCCGGAA[C/G/T]AAGACTTCCGTCACC | 9100 |
| rs370874620 | snp | C/T | 3.32419e-05 | 0.00407675 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84778980 | TGGCTGGCTGCGCAT[C/T]GATGACCAGACAGTC | 9100 |
| rs370947303 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84709993 | TAGCTGGTTGAGGCC[A/C/G]GGTGCGAGGCTCACG | 9100 |
| rs370962982 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84716864 | CATAATTCATCATAA[C/T]GATCCTTTCACTCTG | 9100 |
| rs370982429 | snp | A/G | 3.31543e-05 | 0.00407137 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84763011 | AAGAAGATGCTGAGG[A/G]ATACTTAGGCTTCAT | 9100 |
| rs370988922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84775780 | GTGGACCTTGAGACC[C/T]CTTCTGTCTCCTGGC | 9100 |
| rs370989451 | snp | C/T | | | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84768270 | AGTTGGATATCCAGT[C/T]AGACAAGATACGCAC | 9100 |
| rs371015781 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84711865 | GCTGGGATTACAGGT[G/T]CGTGCCACCATGGCT | 9100 |
| rs371020734 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84771055 | GAGCGAGACTGTCTC[A/C]AAAAAAAAAAAAAAA | 9100 |
| rs371031271 | snp | A/G | 0.000161987 | 0.00899817 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745409 | CACACCACGGAAAGC[A/G]TAGACTTGGACCCAA | 9100 |
| rs371031725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84757142 | CATGACAGGTGCTAT[C/T]TCTGCTGGGTGTCAT | 9100 |
| rs371031738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84753975 | AGCAAGGAGGGGAGG[C/T]CTCATGCAGCTAGTA | 9100 |
| rs371035288 | snp | A/T | | | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744683 | GAAGTCATTGAACCC[A/T]GTGACACTTTGCCGA | 9100 |
| rs371050830 | snp | A/C | 1.67539e-05 | 0.00289425 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745356 | GACAAATACTTGAAT[A/C]CTCGGGTGAGGGCAC | 9100 |
| rs371134091 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84756025 | AGCTTCCATTTGGTG[G/T]CTTCAACCCCTGACC | 9100 |
| rs371142069 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84768878 | AAAGGTAAGATTCTT[G/T]AGTCTTTCAGTCTTC | 9100 |
| rs371187327 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84775589 | CGACACCTGGTCACC[C/G]AGCCAGGTTGGGTGA | 9100 |
| rs371188210 | in-del | -/AAACAAAC | 0.0154538 | 0.0865337 | intron-variant | USP10 | GRCh38.p7 | 16:84727460 | GTGTTAGCTTTAAAA[-/AAACAAAC]AAACAAACAAACAAA | 9100 |
| rs371197889 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84759819 | TGATATTCTACTTAG[C/T]CATCAAAGCTCTTTA | 9100 |
| rs371206936 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84727944 | TCTAGAATTTTCCCT[C/T]CCAGCACAGGATCCA | 9100 |
| rs371229146 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84714990 | GCTGGAGTGCAGTTC[A/G]CAGTCTCGGCTCACT | 9100 |
| rs371270220 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84771032 | ACTGCACTCCAGCCT[C/T]GATGACAGAGCGAGA | 9100 |
| rs371270434 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718464 | AATTTAGTTGCATTA[C/T]AGTTTTTCTTCTGGC | 9100 |
| rs371292425 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84766343 | CTGTGGAGTGTCCAC[A/G]GCAGCTGGGTGGTCA | 9100 |
| rs371340605 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84747822 | TCTGCTCGCTTCAGC[A/C]TCCCAAAGTGTTGGG | 9100 |
| rs371364032 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84726815 | CCTTGTACTTTGCTC[C/T]CCCGAATCGCAGGCA | 9100 |
| rs371371167 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84753939 | GAAGTGATCATTGGC[A/T]GAGGGGTGTTGAGGG | 9100 |
| rs371380648 | snp | A/G/T | 0.00358923 | 0.042236 | intron-variant | USP10 | GRCh38.p7 | 16:84709429 | GCACCATCCAACCTT[A/G/T]CAGCCTTTGTTAGAT | 9100 |
| rs371386983 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84732969 | ATAGATATTTTTAAA[C/G]ATCATTAATCAGGAT | 9100 |
| rs371486208 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84737284 | ATAACTATTAATAGA[C/T]GACAGTTTTTTCCCT | 9100 |
| rs371486448 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84708614 | TGAATTTTTCTCCAT[C/T]TTCTTCAAAATCATG | 9100 |
| rs371504463 | in-del | -/AG | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84736353 | ATTCTGCCTTCCTGC[-/AG]AAGCGCCTCCTGCCA | 9100 |
| rs371552822 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84764394 | TTGCTCCCCTGCCTG[C/G]TCTTCTCTTGCACTT | 9100 |
| rs371585077 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84753195 | TGTGTGGCCCAGGCT[C/G]ATCTTGGAACTCCTG | 9100 |
| rs371586311 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84735158 | TGCTTCAGCCCCTGA[A/G]TAGCTGGGATTACAG | 9100 |
| rs371587667 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84714738 | ATTGTAAACTGGAAG[A/T]TGAACGTCCTTAATT | 9100 |
| rs371592716 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84776852 | GAGTTTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 9100 |
| rs371593918 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718747 | GGCAACAGAGCAAGA[C/G/T]TGTCTGACAAAAAAA | 9100 |
| rs371602728 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84741806 | CCAGTGCCTGTTCGA[A/C]TGTACAGAGCCTGTG | 9100 |
| rs371625146 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718880 | TCACTGCAACCTCCA[C/T]CTCCTGGGTTCAAGC | 9100 |
| rs371630614 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | USP10 | GRCh38.p7 | 16:84705255 | TTTTTTTTTTGAGAC[A/G]GAGTCTCGCTCTGTC | 9100 |
| rs371692007 | in-del | -/TG | | | intron-variant | USP10 | GRCh38.p7 | 16:84778092 | TTTTAAGTAAATAAC[-/TG]TGTGTGTGTGTGTGT | 9100 |
| rs371694161 | snp | C/T | 1.66275e-05 | 0.00288331 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744985 | GAAAGATGGTGGCGA[C/T]GATAGTATCTCCACA | 9100 |
| rs371704368 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84712373 | GCTGGCCTGGCTGCT[C/T]TTTCGGGTCAGGAAG | 9100 |
| rs371707239 | snp | C/T | 2.39352e-05 | 0.00345934 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84760214 | TTCGCCCTGGAGCTG[C/T]CTTTGAGCCCACATA | 9100 |
| rs371723423 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84758816 | TAATGCTGTATCCTT[A/C]CTGGACGCCGTCCGC | 9100 |
| rs371730778 | snp | G/T | 3.31752e-05 | 0.00407265 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744788 | AAAATAACCCCTGAT[G/T]GTATCACTAAAGAAG | 9100 |
| rs371734969 | in-del | -/TC | 0.0178098 | 0.0926698 | intron-variant | USP10 | GRCh38.p7 | 16:84724254 | TGGTAAAAGTGGGTT[-/TC]TGTTAAGTGAATCAT | 9100 |
| rs371792041 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84714165 | CAGTTGAGAAGCGTG[G/T]AGGGCTTGAACAGTG | 9100 |
| rs371801199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751964 | TGCCTTTGAGTTGAT[A/G]AACAATTTCAGTGGG | 9100 |
| rs371807009 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84769492 | TTCAGTGAATGAGCT[A/G]AGAAGAGTCTGGCGG | 9100 |
| rs371901526 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84769960 | CTTCCAGAAAGAAGG[C/T]GGGCCAGGTGTGGTG | 9100 |
| rs371920485 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84710139 | GCCGGGCGTGGTGGC[G/T]CATGTCTGTAATCCC | 9100 |
| rs371926879 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84752389 | AAGGTAAAATAGATA[C/G]ACCAATGGCAATGAC | 9100 |
| rs371952834 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84774212 | CATGCCACTGCACTC[C/T]AGCCTGGGCAACAGA | 9100 |
| rs371957718 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84747509 | GCAAATGATAGGCCA[C/G]ACGTCGTTATTTTGG | 9100 |
| rs371959609 | snp | A/G | 0.00021539 | 0.0103754 | intron-variant | USP10 | GRCh38.p7 | 16:84775242 | TGAGTAAATTTGTAC[A/G]ACATTACTTCTTCAT | 9100 |
| rs372006668 | snp | A/G | 0.000167986 | 0.00916322 | intron-variant | USP10 | GRCh38.p7 | 16:84775140 | AAAGTGCTTCAAGCC[A/G]TTGATATTTTGTTTT | 9100 |
| rs372014304 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84729361 | TTAGGATTCCCCTAG[C/T]TTGTGATATCGATGA | 9100 |
| rs372029593 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84741063 | GGCCCTTACTGGCCT[C/G]CAGGAAACTGATGCC | 9100 |
| rs372065559 | snp | A/C/T | 6.74256e-05 | 0.00580594 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745095 | TGCCCCCGTCAGTTA[A/C/T]GCCCAGGACTTGTAA | 9100 |
| rs372066961 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84740995 | TTGATTGCAGGCTGC[C/G]CTTGCACAATTCAAA | 9100 |
| rs372131758 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84710499 | AGGTAGCCCTTCAGT[A/G]TCCTCAGTGGTAATT | 9100 |
| rs372140228 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84767402 | GCGCCCTTCTTGGAA[A/G]GGTGGCAGCCTTTTT | 9100 |
| rs372156411 | in-del | -/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84701937 | CATAATTTTCTTCTT[-/C]TTTTTTTTTTTTTTT | 9100 |
| rs372159774 | in-del | -/T | 0.00398564 | 0.0444627 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698481 | CCAGCTTAAAAGACA[-/T]TATCAGGATCCAAGC | 9100 |
| rs372199713 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84705616 | TCTTCCTGATCTGAT[A/G]GTGCTAGATTTTTGT | 9100 |
| rs372208146 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84711161 | TGGCATTCATTAAGT[C/G]CATGATTATGCCTTT | 9100 |
| rs372329595 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84736243 | ATATGCTTTTTCTCC[A/G]TTGTTAGGAGCTTGA | 9100 |
| rs372405516 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84716529 | CATAGGTAAATGAGA[A/G]TTACTATGAAATATG | 9100 |
| rs372432376 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84733884 | TGTGCTTTAAAGTGT[C/T]ACGTAAATGGTATAC | 9100 |
| rs372456652 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84734815 | AAATTGAGGCACTGA[A/G]TTTTGTATATGTGTG | 9100 |
| rs372457080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84731401 | GATTTTAGTTTATTT[A/G]TTCTTAATATTTGCA | 9100 |
| rs372460340 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84772368 | TGTGCATTTTCTTAA[A/G]AGGAGCATTGGTAGA | 9100 |
| rs372463921 | snp | A/G | | | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719566 | GCCTTTGTCCAATAT[A/G]GTTTATGCTGCTCCC | 9100 |
| rs372470490 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84765096 | AAAACCAGCTAACCA[A/C]ACCATGTGTTTTGGT | 9100 |
| rs372478454 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84719081 | ACAGGCATGAGCCAC[C/G]GCGCCCGGCCAGTTT | 9100 |
| rs372509439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84729216 | AACCTTCACATTTGT[A/G]TGGATTATTTTATCA | 9100 |
| rs372519254 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84749547 | GAGTTCGAGGCCAGC[C/G]TGGGCAACATACTGA | 9100 |
| rs372532653 | snp | A/G | 0.000287687 | 0.01199 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84768241 | TGCCACTTTGCAGCC[A/G]TTTTTCACGTTGCAG | 9100 |
| rs372565903 | snp | A/G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84710900 | TTTTTGTTTTAACTT[A/G/T]TTGAGCCCTTTCGCA | 9100 |
| rs372644777 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84728088 | CTTTTGATAACATTC[C/T]TCATTTTACCAAACA | 9100 |
| rs372650362 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84704463 | GTCACTTTAGTGCCA[C/G]TTCAGCAGTGTAGAT | 9100 |
| rs372650828 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717864 | CTTAATTTAATTCAT[A/T]CAGTTGCTATTCTTG | 9100 |
| rs372661072 | snp | A/G | 1.66302e-05 | 0.00288355 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744848 | CCAGGCTCTGCCCTC[A/G]CTTTGGATGGAAGTT | 9100 |
| rs372668321 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84751039 | ACAGTTATGTGCTGC[C/T]TTAATGATGTTTCAG | 9100 |
| rs372686428 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84757421 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 9100 |
| rs372692628 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84771624 | CTGTAATCTCAGCAC[G/T]TTGGGAGGCTGAGGC | 9100 |
| rs372707225 | snp | C/T | 3.31516e-05 | 0.0040712 | missense, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779038 | AAACCAACTGCTGAA[C/T]GCACAGCCTACCTCC | 9100 |
| rs372713314 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84773298 | GGCTTGATTGGGACT[G/T]TGATTAGCTAGAGAG | 9100 |
| rs372729467 | snp | C/T | 4.97905e-05 | 0.00498926 | intron-variant | USP10 | GRCh38.p7 | 16:84740415 | GGGAATTTGGCCATA[C/T]GTGCTGGGTGGGCAG | 9100 |
| rs372738444 | snp | C/T | 3.73546e-05 | 0.00432156 | intron-variant | USP10 | GRCh38.p7 | 16:84760134 | TCATTTATGAGTTCA[C/T]TGTAGTTAGGAAAAC | 9100 |
| rs372763112 | snp | G/T | 0.000120178 | 0.00775077 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84768269 | CAGTTGGATATCCAG[G/T]CAGACAAGATACGCA | 9100 |
| rs372782185 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84759229 | GGTTTATTCCTTTTC[C/G]TGGTGACATATCTAA | 9100 |
| rs372815963 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84775900 | TCATCTTTTATGCCT[C/G]TGAGTCTTTACCTCT | 9100 |
| rs372838753 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84716573 | CAGAAATAGGGTTTA[C/G]AAACACTTCCTGAGG | 9100 |
| rs372870864 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84702118 | CTGGAGTGCAGTGGC[A/G]TGATCTCGGCCCACT | 9100 |
| rs372890507 | snp | C/G | 0.000163987 | 0.00905354 | missense, nc-transcript-variant, intron-variant | USP10 | GRCh38.p7 | 16:84759442 | CCAAAGTGCAAAGGC[C/G]TTGTACGTCAACACC | 9100 |
| rs372939681 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84769681 | CTGCTTATGCTGTTT[C/T]TTGAGCCAGCTATGG | 9100 |
| rs372963197 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84747795 | TGGCCTCAAACTCCT[G/T]ACCTCAAGTGATCTG | 9100 |
| rs372968687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84712853 | TTGGTCTCTTTCTCA[A/G]CAAGTGTAGTCTGGA | 9100 |
| rs373087834 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84755602 | AATCACGCCACTGCA[A/C]TCCAGCCTGGGTAAT | 9100 |
| rs373088495 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84726741 | TGGTGGAGGGGAATA[A/C]ATAGCTTCTCTAGTT | 9100 |
| rs373097833 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84770502 | AGTTGGCTGGGCGAG[A/G]TGGCTCACACCTGTA | 9100 |
| rs373115710 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84703159 | TGAGACCGGTAACTC[A/C]GCATTTTAGCAAAGA | 9100 |
| rs373119092 | snp | C/T | 0.000296868 | 0.0121797 | intron-variant | USP10 | GRCh38.p7 | 16:84760312 | ACTAGTATCAAGTGT[C/T]GCCTTTTGTTCCAGT | 9100 |
| rs373134780 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84720952 | AGGCTGGAGTGCAGT[A/G]GCGCGATCTCAGCTC | 9100 |
| rs373143811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84730338 | ATTTTGAAGATCTCT[C/T]GCTGTCTGTACCTAA | 9100 |
| rs373164640 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84741492 | TACAAATGCCCCATG[A/G]TGTTCCCATGCACAT | 9100 |
| rs373203282 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84725464 | GAGTGCAAATGGCAC[A/G]ATTTCCGCTCACTGC | 9100 |
| rs373222407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84753042 | CATGATCATAGCTCA[C/T]TGCAGCCTTGATCTC | 9100 |
| rs373224037 | in-del | -/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84714538 | TTTTCCTTTGCGATT[-/G]TTTTTTTTTTTAGAT | 9100 |
| rs373228637 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | USP10 | GRCh38.p7 | 16:84775607 | CCAGGTTGGGTGAGC[A/G]CGCCCCCAGCCGGTG | 9100 |
| rs373252988 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84708404 | TGCTGTGAGACAAGA[A/T]CACGCCACTTCACTC | 9100 |
| rs373259732 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84776321 | TAGCGGTGGGGGCCC[A/C]GGGGTGAGGGCCCAG | 9100 |
| rs373270882 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84758078 | AGTGATGTCCACTCA[G/T]GGTGAACCTGAGGCT | 9100 |
| rs373334601 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84705526 | GTGAGCCACCACACC[C/T]AGCCACTCCTGTGCC | 9100 |
| rs373346941 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84746054 | GTGCTCCTTTTTTAT[A/G]TTTCTTAAGATACAA | 9100 |
| rs373348121 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84703323 | TTATTGATGTCATTT[A/G]TAGTGAAATCTCCAC | 9100 |
| rs373349766 | snp | C/G | 0.000167986 | 0.00916322 | intron-variant | USP10 | GRCh38.p7 | 16:84745696 | TGAAAAGATACAAAT[C/G]TAGAGTGAAGATGGG | 9100 |
| rs373355410 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717625 | CTAGGTAGGTAGGAG[G/T]AGGCCACTACCTAGG | 9100 |
| rs373358150 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84775619 | AGCGCGCCCCCAGCC[A/G]GTGATCCCTGCGTCC | 9100 |
| rs373402447 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84722438 | TCTTGTGGGTAAAAT[A/G]TGGTAAGCGTATATT | 9100 |
| rs373409720 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84732928 | TGTGTATCCTATGGA[A/C]ATGCATTTTTAAACT | 9100 |
| rs373429156 | snp | C/T | 0.000497595 | 0.0157655 | intron-variant | USP10 | GRCh38.p7 | 16:84758697 | TCAATTTCTGAAATA[C/T]GCTTCTTCACTCTTT | 9100 |
| rs373500154 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84709818 | AGACTGTGCAGAGGA[A/C]CTGTCTCAAAGCCTG | 9100 |
| rs373509774 | snp | G/T | 1.67874e-05 | 0.00289714 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745341 | TTGGAGTTGCTAATG[G/T]ACAAATACTTGAATC | 9100 |
| rs373519913 | snp | A/G | 0.000182389 | 0.00954785 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764153 | GGAAGAACAAGGTGA[A/G]GGAAGCGAGGATGAA | 9100 |
| rs373544856 | snp | C/T | 4.97905e-05 | 0.00498926 | missense, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84733484 | ATCAATTCTTTGTGA[C/T]TCCTCGATCTTCAGT | 9100 |
| rs373570866 | snp | A/C | 4.97038e-05 | 0.00498492 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84759942 | ACCTCCAAAACCCCG[A/C]CAAGGTTAGTAAAAA | 9100 |
| rs373587941 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84710798 | TGCCACCAAGAGACA[C/T]TGAGTAAGGATCCCT | 9100 |
| rs373590750 | snp | A/C/G/T | 0.000215606 | 0.0103809 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764209 | AGACTTCCGTCACCC[A/C/G/T]CCAGGCGGATTTTGT | 9100 |
| rs373608592 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84731072 | GCAACCTCCACCTCC[C/T]GGGTTCAAGCGATTC | 9100 |
| rs373648775 | snp | A/G | 3.32452e-05 | 0.00407695 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744998 | GATGATAGTATCTCC[A/G]CAGAAGCCCTGGTCA | 9100 |
| rs373691185 | snp | C/T | 1.65605e-05 | 0.0028775 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84772563 | TAAGTCGAAGAGTGA[C/T]TCTGGAAAAACTCCC | 9100 |
| rs373736693 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | USP10 | GRCh38.p7 | 16:84773976 | AAATGGGGGCTGGGC[A/G]CAGTGGCTCACACCT | 9100 |
| rs373757372 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84728470 | TCAGCCTCCCGGGTA[A/G]CTGGGACTACAAGCA | 9100 |
| rs373768584 | in-del | -/GGGGT | | | intron-variant | USP10 | GRCh38.p7 | 16:84757394 | AAGGAGGGAATGAGA[-/GGGGT]GGGGGTGTGTGTGTG | 9100 |
| rs373770197 | snp | A/G | 9.94975e-05 | 0.00705258 | intron-variant | USP10 | GRCh38.p7 | 16:84772506 | TGTTGCAAGTAAGAC[A/G]GGGACGGTGTGTCCT | 9100 |
| rs373776630 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84773124 | ACAAATAAGACGTGG[C/T]ACTTACCAGCCTCAA | 9100 |
| rs373784945 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84750695 | AGCCATTTTGTATTT[A/G]ATGTTTTGCTTTCAA | 9100 |
| rs373832873 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84727025 | GGCAGAGTTAGCCGC[A/G]GCAGTGTCACAGTTT | 9100 |
| rs373847736 | snp | A/G | 0.000165695 | 0.00910054 | intron-variant | USP10 | GRCh38.p7 | 16:84759982 | TTGATGCTATTACAT[A/G]TTGGGAGTTATGGAG | 9100 |
| rs373865110 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84721001 | CGTATTCAAGCTATT[C/T]TCCTGCCTCAGCCTC | 9100 |
| rs373874429 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84738533 | CTCTCTGCTCCAGGT[G/T]CCTGCCAGCATCAAT | 9100 |
| rs373923706 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84701431 | AATGTATAGCCCAAA[G/T]ATTTTAAGAGATTTG | 9100 |
| rs373943132 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84756513 | CAGGAAAATCACTTG[A/C]ACCCAGGACACAGAG | 9100 |
| rs373943821 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84741849 | GACCTGCCTCTCTTT[C/G]CAGCCTGCTCAGCTG | 9100 |
| rs373948952 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84730637 | ACAGGAAGTGTGTGT[A/T]AGTGGCTTGGAATCT | 9100 |
| rs373959539 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84774216 | CCACTGCACTCCAGC[C/G]TGGGCAACAGAGCAA | 9100 |
| rs373967964 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84760073 | GCCATTCTCAACATT[C/G]AGCCAGGTGGGAGGT | 9100 |
| rs374003605 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84703291 | AGTTTTGCCTTACAC[C/G]GAAAAAATATTTGTG | 9100 |
| rs374018824 | in-del | -/AA | | | intron-variant | USP10 | GRCh38.p7 | 16:84750405 | AGTGAGACTGTCTCA[-/AA]AAAAAAAAAAAAAAA | 9100 |
| rs374054985 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | USP10 | GRCh38.p7 | 16:84751223 | ATATGGCCCAGGTGT[A/G]TAGTTGGCTATACCA | 9100 |
| rs374065069 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84773544 | TACCTTCCCGTGAAG[A/G]CTCAGACACTGTCTC | 9100 |
| rs374068526 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84747494 | AGTTCTCTTAAATGA[A/G]CAAATGATAGGCCAG | 9100 |
| rs374076706 | in-del | -/CA | | | intron-variant | USP10 | GRCh38.p7 | 16:84766332 | TTCTGGTGCTCTGTG[-/CA]GAGTGTCCACGGCAG | 9100 |
| rs374079363 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | USP10 | GRCh38.p7 | 16:84721791 | CAACCTCCGCCTCCC[A/G]GGTTCAAGCAATTCT | 9100 |
| rs374083269 | in-del | -/GTTTT | | | intron-variant | USP10 | GRCh38.p7 | 16:84721715 | GTTTTGTTTTGTTTT[-/GTTTT]AGAGATTGAGTCTTG | 9100 |
| rs374140741 | in-del | -/G | | | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779981 | TGAAATTCATGGGGG[-/G]CATGAGTTTGCCTGC | 9100 |
| rs374177225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84728152 | CTTTTGGAGAAGGAG[A/G]TGGTGAAACCAGAAC | 9100 |
| rs374200706 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84714480 | TGCGCCACCGTGCAC[A/G]GCTTTGCATTTCTTA | 9100 |
| rs374207952 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84704272 | TGCTGAGGACACTTA[C/T]TACTGGTACTATACC | 9100 |
| rs374221523 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84742372 | TATTCACAGCTTTCT[C/G]TCCCCTCCCTCCATG | 9100 |
| rs374227178 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84728500 | ATGTGCCACCACGCC[C/T]GGCTAATTTTTGTAT | 9100 |
| rs374252609 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84748451 | TGGGACTACAGGTGC[C/T]TGGCACCACGCCAGG | 9100 |
| rs374263423 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84714549 | ATTGTTTTTTTTTTT[-/T]AGATCTCAAGAGCCT | 9100 |
| rs374266546 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84724800 | GTTGATGCTCAGTGC[A/G]TATTGTTAAATTGGC | 9100 |
| rs374314445 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84778169 | TTTTTAAAGGCAAAT[G/T]CGTAACTACCAGCAC | 9100 |
| rs374323604 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84757160 | TGCTGGGTGTCATCA[C/G]ATGCAGGCTTGGGGT | 9100 |
| rs374356066 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP10 | GRCh38.p7 | 16:84760821 | GAGAGTGACTTGGGC[C/T]GCCCTTAGCACCGTT | 9100 |
| rs374358369 | in-del | -/A | | | intron-variant | USP10 | GRCh38.p7 | 16:84730531 | AATAGGAGAAAAAAA[-/A]CTCAGTGAACCGTTT | 9100 |
| rs374381479 | in-del | -/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84770772 | GCGAGACTCCGTCCC[-/C]AAAAAAAAAAAAAAA | 9100 |
| rs374404036 | in-del | -/TTTC | | | intron-variant | USP10 | GRCh38.p7 | 16:84746856 | TAAACTTTTTGACTC[-/TTTC]ATGAGAACATTTAGC | 9100 |
| rs374404290 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84753291 | TCTTTAATATGTCAA[C/G]ATGTTTAAAACTTGT | 9100 |
| rs374444482 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84740950 | TGCTTAAGTACCCAG[A/C]GTTGGAATACCAACA | 9100 |
| rs374490329 | snp | C/G | 0.000165986 | 0.00910854 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84763037 | TTCATTCTAAATGGA[C/G]TTCATGAGGAAATGT | 9100 |
| rs374549096 | snp | A/G | 0.00142847 | 0.026687 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84778923 | CGGCAACAGTGCGAC[A/G]GGCGGCCATTACACT | 9100 |
| rs374554606 | snp | A/G | 1.6625e-05 | 0.00288309 | intron-variant | USP10 | GRCh38.p7 | 16:84740278 | TTAACATTTTGTTGA[A/G]TTAAAATTTGTTTTC | 9100 |
| rs374580989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84709871 | AATTTGTGGCTGAAA[C/T]GGTGTGTAGGGTGAA | 9100 |
| rs374599866 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84716825 | TGGGGAGTGACCGCA[C/T]GTCCTGGTCTAAACT | 9100 |
| rs374612375 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84771686 | CCAGCCTGGCCAACA[C/T]GGTGAAACCCCTTCT | 9100 |
| rs374644440 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84738276 | TTTTGACTCAGAAAA[A/C]GATGATTTCTTGATG | 9100 |
| rs374723971 | snp | C/T | 1.65974e-05 | 0.0028807 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764219 | CACCCGCCAGGCGGA[C/T]TTTGTTCAGACTCCA | 9100 |
| rs374747316 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84710195 | GAATCGCTTGAACCC[A/G]GGAGGCAGAGGTTGC | 9100 |
| rs374763173 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84778646 | AATATGTGGTTAATA[C/T]GCGTACATGCACACA | 9100 |
| rs374772433 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84709442 | TTGCAGCCTTTGTTA[C/G]ATGTTACTGTCTTTA | 9100 |
| rs374787833 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84720879 | GGGCCACCGCGCCCG[G/T]CCAATGATGCACAAT | 9100 |
| rs374834876 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84740721 | GCCTGCTGGCTCCAG[C/T]GCCAGCTAGCTTCTG | 9100 |
| rs374840067 | in-del | -/AG | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84705837 | CGATTCTCCTGCCTC[-/AG]TCTCTCAAGTAGCTG | 9100 |
| rs374949226 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84778224 | CTCCACGCTCAAGCA[A/T]CCGTGGTTAGCAGTC | 9100 |
| rs374960440 | snp | C/G/T | 4.97731e-05 | 0.00498839 | intron-variant | USP10 | GRCh38.p7 | 16:84758852 | CAGCTTGTTGCAGCT[C/G/T]TCCCTCCTTTGGGTG | 9100 |
| rs374962856 | snp | C/T | 0.00010016 | 0.00707602 | intron-variant | USP10 | GRCh38.p7 | 16:84763109 | TTATGGTCCACTTGC[C/T]GCAGAGTTGTGCAAG | 9100 |
| rs375066408 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84737552 | CCACAACCCATCTGG[C/T]ATTCCTGCAGGTGCG | 9100 |
| rs375070253 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84709524 | TCATAATCACATTGC[C/T]TTTTGGGATCATACT | 9100 |
| rs375114598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718349 | GCCTCAAAGTTATTG[A/G]CTCAAGGGATCCTCC | 9100 |
| rs375145920 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84755154 | TTTCAGGCAGATCTT[G/T]TATGCCTGGCCCTGG | 9100 |
| rs375155743 | snp | C/T | 0.00024667 | 0.0111029 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84760236 | GCCCACATATATTTA[C/T]AGACTCCTGACAGTT | 9100 |
| rs375207314 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84767924 | GGCAGAGGACCCTGC[A/G]GCCTTCCGCAGTGTT | 9100 |
| rs375223842 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84733985 | TGATTTCCAGTGCTC[A/G]GTACCACTGATTGAA | 9100 |
| rs375232249 | in-del | -/TTG | | | intron-variant | USP10 | GRCh38.p7 | 16:84744047 | TATATATAGGATTCT[-/TTG]TTGTTGTTGTTGTTG | 9100 |
| rs375237058 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84776539 | AGGTCTGAGTCCTCA[A/G]ACTCTGCAGCCAGCC | 9100 |
| rs375262136 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84710167 | CCCAGCTACTTGAGA[G/T]GCTTAGGCAAGAGAA | 9100 |
| rs375263157 | snp | A/G | 0.000762145 | 0.0195062 | intron-variant | USP10 | GRCh38.p7 | 16:84775260 | ATTACTTCTTCATTA[A/G]AACACTGATGAAGGG | 9100 |
| rs375280033 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84752427 | TGCAGGTCAAGTTTC[A/G]ACCTAGAAGTTGCCT | 9100 |
| rs375293690 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84737356 | TTGATTTTTGAACTT[C/T]GTATTCTTACAAATA | 9100 |
| rs375328756 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84706382 | TTAGGTTCACAGCAA[A/G]ATTGAGAGAAAAGTA | 9100 |
| rs375380113 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84701833 | AACGTAAATGTTAGC[A/G]ACACTTTGGGTTTAT | 9100 |
| rs375383405 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84716032 | ACCAGAGCACTGTGG[C/T]GAGGAGGGTGGTATG | 9100 |
| rs375384005 | snp | A/G | 0.000165986 | 0.00910855 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744966 | CTGGATATTACAGCT[A/G]TTTGAAAGATGGTGG | 9100 |
| rs375389637 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84731221 | TCTGACCTCATGATC[C/T]GCCCACCTCGGCCTC | 9100 |
| rs375395967 | snp | C/T | | | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719267 | TTTTTAACTGGGAGG[C/T]ATAACTGAATGGAGA | 9100 |
| rs375414745 | in-del | -/A | | | intron-variant | USP10 | GRCh38.p7 | 16:84760994 | TTTGAAGAAGAGTGA[-/A]TGTCGAGGGCATCGT | 9100 |
| rs375425897 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84767483 | CTTTTTGTAAGACAT[C/T]TTTATAGGAGGAAAA | 9100 |
| rs375437757 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84711902 | TTTTTGTATTTTTAG[A/C]AGAGACGGGGTTTCA | 9100 |
| rs375439886 | snp | C/T | 3.37206e-05 | 0.00410599 | intron-variant | USP10 | GRCh38.p7 | 16:84762965 | ATCAGTTCACAGTAA[C/T]GTGATTATATTTGAC | 9100 |
| rs375461718 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84754401 | GCGTTTAACGACGTC[A/G]TACCAGAATGGCCTT | 9100 |
| rs375464582 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84736660 | ATCTCAGCTTTGGAA[G/T]TAGCACACATCCCAA | 9100 |
| rs375574756 | snp | C/G/T | 8.28919e-05 | 0.00643732 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779001 | CCAGACAGTCAAGGT[C/G/T]ATCAACCAGTACCAG | 9100 |
| rs375606855 | snp | C/G | 0.000437904 | 0.0147905 | intron-variant | USP10 | GRCh38.p7 | 16:84760006 | TATGGAGACAGATGA[C/G]TTAAATTTGGTAAAT | 9100 |
| rs375612898 | snp | C/T | 0.000165986 | 0.00910855 | missense, intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84740349 | TGTGTGGCACACAGG[C/T]TGTGGATAAACTACC | 9100 |
| rs375620809 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717476 | ACATTGCTTAAACAT[G/T]TTAAACTGCTTTTTA | 9100 |
| rs375624150 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84752771 | CGAACTTCATAAAGC[A/G]TTAGTGTCTCCTCCA | 9100 |
| rs375625029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84742707 | AGCTCTCTGCCATGC[A/G]GTGCAAGGCACATGG | 9100 |
| rs375626977 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84715693 | TAACTGGCTTACACC[A/G]TAAACTAGAGATTTA | 9100 |
| rs375696525 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84747511 | AAATGATAGGCCAGA[C/T]GTCGTTATTTTGGGC | 9100 |
| rs375761746 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84700925 | TCTTCTCCCCCCTCC[G/T]CCATTATAATTATTC | 9100 |
| rs375765095 | snp | C/G | 2.02854e-05 | 0.0031847 | intron-variant | USP10 | GRCh38.p7 | 16:84764077 | GTAAGCAGATGCTCT[C/G]CTTTTCAGAACTTAC | 9100 |
| rs375772969 | snp | A/G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84731435 | AACTTCACAGCTGCC[A/G/T]TGTGTTTCTTGTATT | 9100 |
| rs375817370 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84731360 | AGTAGCCACGTTTCT[A/G]CTATTGATATTAAAC | 9100 |
| rs375833232 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84721846 | GGGACTACAGGCACA[C/T]GCCGCCACACCTGGC | 9100 |
| rs375848107 | snp | A/G | 1.71021e-05 | 0.00292416 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764103 | CTTACGATTTCCAAC[A/G]GCCCCAAAAACCACT | 9100 |
| rs375880108 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84732804 | GGTAGGCACTTGCCA[G/T]ACTCACATCCGTGCA | 9100 |
| rs375899400 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718523 | CAGCACTTTGGGAGG[C/T]CAAGGCGGGTGGATC | 9100 |
| rs375916501 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84723767 | GAATTTCACCCATTT[A/G]AAGTGTATATTTCCA | 9100 |
| rs375923938 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84777899 | CATTCCCCGCGGAAT[A/G]CTGCCGGACAGCCGC | 9100 |
| rs375942583 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84747948 | ACAAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 9100 |
| rs375960997 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84735348 | TACACATGTGGATGG[A/G]TGGGTACCTGTTTGC | 9100 |
| rs375961307 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84714752 | GATGAACGTCCTTAA[C/T]TCATTGATTATTTTT | 9100 |
| rs375964859 | snp | G/T | 1.6582e-05 | 0.00287936 | intron-variant | USP10 | GRCh38.p7 | 16:84775153 | CCATTGATATTTTGT[G/T]TTCCAGAACTGCTTT | 9100 |
| rs376021515 | snp | C/T | 8.47264e-05 | 0.00650815 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779093 | TGTAAACCCTGTGTG[C/T]GCTGTGTGTGCGCCC | 9100 |
| rs376028876 | snp | C/G | 1.6588e-05 | 0.00287988 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744699 | GTGACACTTTGCCGA[C/G]AACCCCCAGCTACAG | 9100 |
| rs376037233 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84724544 | TTGTCTACTTTGTTC[C/G/T]CTTCTCAGGACCTCT | 9100 |
| rs376048080 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84711169 | ATTAAGTCCATGATT[A/G]TGCCTTTTAAGCAAG | 9100 |
| rs376060520 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84738489 | TGAGACACACATGGC[C/T]GCTGTGTCCACTGCC | 9100 |
| rs376082373 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | USP10 | GRCh38.p7 | 16:84770816 | CTGATGCCTGTAATC[C/G]CAGCATTTTCGGAGG | 9100 |
| rs376083849 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84760573 | CAGAACCCAGCTTTC[A/T]AGTCAGTTCTCTTAA | 9100 |
| rs376089624 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84725546 | GCTGAGATTAGAGGC[-/G]CCTGCCACCATGCCC | 9100 |
| rs376100125 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84713963 | GGGGGTTGGCTGGGA[A/G]GGTGGATGGGTGCGT | 9100 |
| rs376120530 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | USP10 | GRCh38.p7 | 16:84756551 | TGAGCCAAGATTGCA[C/T]CACTGCACTCCAGCC | 9100 |
| rs376131026 | snp | C/T | 0.000167986 | 0.00916323 | intron-variant | USP10 | GRCh38.p7 | 16:84759968 | AAAAATGAGTTTTGT[C/T]GATGCTATTACATAT | 9100 |
| rs376132891 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84734162 | TTACTGGGTTCTGTG[G/T]ACCGAGCCTCTTTAG | 9100 |
| rs376147375 | snp | C/T | 0.000159987 | 0.00894248 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779053 | CGCACAGCCTACCTC[C/T]TGTATTACCGCCGAG | 9100 |
| rs376156186 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84753034 | TGCTGTGGCATGATC[A/G]TAGCTCACTGCAGCC | 9100 |
| rs376175235 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84754381 | AGTCTGAAAAGGTTT[A/G]TTCTGCGTTTAACGA | 9100 |
| rs376186125 | snp | A/G | | | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84733087 | GGAAATGGAGGTAGT[A/G]GCATGAGTCAGCAGA | 9100 |
| rs376195179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84775884 | TTTCTCTTTTATAGC[A/G]TCATCTTTTATGCCT | 9100 |
| rs376211856 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84770226 | GTGTTACCAGATGAG[G/T]CCAGGACCACTTTCA | 9100 |
| rs376231447 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84766181 | AAGAACCTCAGAAAC[C/G]TGCGCTGACGCCCTC | 9100 |
| rs376269292 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84726115 | TCTCCTATTTCTATC[A/T]GTCCTTTTGAAGGCA | 9100 |
| rs376269529 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84746421 | AGTACTACACAAATA[C/T]AGGTGGTAGAGCCTT | 9100 |
| rs376281243 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84732944 | ATGCATTTTTAAACT[A/G]AGAAGTTATATAGAT | 9100 |
| rs376290801 | snp | A/C/G/T | 0.000588157 | 0.0171386 | intron-variant | USP10 | GRCh38.p7 | 16:84760320 | CAAGTGTTGCCTTTT[A/C/G/T]TTCCAGTGTTTGTGT | 9100 |
| rs376292701 | snp | A/G | 0.000167986 | 0.00916322 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84759916 | ATGAATGAGTTCACT[A/G]ATATGCCAGTACCTC | 9100 |
| rs376293643 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84767098 | GAAGTCTTCAAACTG[A/T]AAAGGAGCATGGAGA | 9100 |
| rs376317218 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84741000 | TGCAGGCTGCCCTTG[A/C]ACAATTCAAACTTGT | 9100 |
| rs376365485 | snp | A/G | 5.02803e-05 | 0.00501374 | intron-variant | USP10 | GRCh38.p7 | 16:84733396 | AAGTATATAATTTGT[A/G]TATTTTATGTGATCA | 9100 |
| rs376446964 | snp | A/G | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717701 | TGGATAGTAACTGTA[A/G]AGTTGAAGAGGAGAT | 9100 |
| rs376487293 | snp | C/T | 0.000116118 | 0.00761876 | intron-variant | USP10 | GRCh38.p7 | 16:84772511 | CAAGTAAGACAGGGA[C/T]GGTGTGTCCTGGTGT | 9100 |
| rs376553590 | snp | C/T | 0.000216214 | 0.0103952 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84778977 | GAATGGCTGGCTGCG[C/T]ATCGATGACCAGACA | 9100 |
| rs376558703 | snp | A/G | 4.96923e-05 | 0.00498434 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84775214 | GCCACCGAACCTATC[A/G]GCTCTTTGCAGGTGA | 9100 |
| rs376574242 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84750646 | CCTCATATACTAGAC[A/G]AAATTGTATCAGATG | 9100 |
| rs376583541 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84709148 | TTCTCTCGCGGAGGA[A/G]TTTATGGGTCCATTG | 9100 |
| rs376624983 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84764941 | AGAGAGAAAAAAAAA[A/T]ATATATATATATATT | 9100 |
| rs376636244 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84713624 | GCTCAGTAAATATTT[A/G]TTAACAAACACCTTC | 9100 |
| rs376655203 | in-del | -/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84774472 | CTGAAGTTTTGTTTT[-/G]TTTTTTTTTTGTTTG | 9100 |
| rs376656490 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84735214 | GTGTGTGTGTGTGTG[-/T]GTGTGTGTGTGTGTG | 9100 |
| rs376662018 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699162 | CTTACGCGTTATGAC[A/G]TATTTGTCTTATTCA | 9100 |
| rs376665649 | snp | A/T | 0.00220644 | 0.0331414 | intron-variant | USP10 | GRCh38.p7 | 16:84768371 | GAGGTATGTTCACAC[A/T]TGATTTTGAACCTTT | 9100 |
| rs376676630 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84777693 | CTCTAGCCAGCCAAG[A/G]TCCCTGGCCCAGAGA | 9100 |
| rs376681864 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84763749 | GATCCAGTGGCATTG[C/T]GCCTGTTGTGATTGG | 9100 |
| rs376685191 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | USP10 | GRCh38.p7 | 16:84705262 | TTTGAGACGGAGTCT[C/T]GCTCTGTCGCCCAGG | 9100 |
| rs376706246 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84720522 | TGGGACAGAGGCTTC[A/T]GAGTGGTGCACAGTT | 9100 |
| rs376709304 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84729714 | GCTCACTTTTAAAAG[A/C]TCATGCATTTAAGGA | 9100 |
| rs376731163 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84717144 | ATTCCTAGGCTGCTG[A/G]CCTGGTGACCTCACT | 9100 |
| rs376754729 | snp | A/G | 0.000182808 | 0.00955879 | intron-variant | USP10 | GRCh38.p7 | 16:84758676 | AATGTTCTTCACTAG[A/G]TGTCATCAATTTCTG | 9100 |
| rs376790358 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84739010 | GTTCTTTTGTTCTGC[C/G]CTCAGGTAGCAGTTT | 9100 |
| rs376798108 | snp | A/G | 3.31862e-05 | 0.00407333 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764216 | CGTCACCCGCCAGGC[A/G]GATTTTGTTCAGACT | 9100 |
| rs376809667 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84750079 | ACTGGTCTGAGAGGA[G/T]ATGGTTGCCATTTAT | 9100 |
| rs376819227 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84739593 | CTAAACTTTCTTACA[C/T]CCAATGTGTCCATTG | 9100 |
| rs376846675 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84774653 | TTTTTTGTATTTTTA[A/G]TAGAGACGTGGTTTC | 9100 |
| rs376861194 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84705620 | CCTGATCTGATGGTG[C/T]TAGATTTTTGTTTTC | 9100 |
| rs376867731 | snp | C/T | 0.000337975 | 0.0129951 | intron-variant | USP10 | GRCh38.p7 | 16:84759339 | TGTTCATTTCCTTTA[C/T]GCTTCCTTACTGCCA | 9100 |
| rs376885391 | snp | A/C/T | 0.00159649 | 0.0282165 | intron-variant | USP10 | GRCh38.p7 | 16:84727715 | AAATATACAGACATA[A/C/T]AATATTTTTCCAAAC | 9100 |
| rs376892765 | in-del | -/CTT | | | intron-variant | USP10 | GRCh38.p7 | 16:84772053 | TGCATTTTTCTTCTT[-/CTT]TTTTCTTTTTTTCTG | 9100 |
| rs376924490 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84765992 | CATTGGAGCCTAATT[G/T]CCTTTCTGAGGCCTT | 9100 |
| rs376950513 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84700415 | GGCTGGACCGCGGGG[A/C]GAGCCCGGGGTGTGG | 9100 |
| rs376962249 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84744209 | CAGAAGCTGATTTAA[C/T]CATGTTTTAAGTCCC | 9100 |
| rs376972081 | snp | A/G | | | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84720062 | CTTGATCTTAACACC[A/G]GAAGGAGAGGAGTCT | 9100 |
| rs376980480 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84773179 | CACTTTTTGAAAGCA[A/G]TTTTAAAGAGCCCCA | 9100 |
| rs376986807 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84750897 | ATTGTTAGTCAAAAC[C/G]TGTTTATATGATTTT | 9100 |
| rs376994211 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | USP10 | GRCh38.p7 | 16:84772786 | TCAAGAGTGAGGACA[G/T]TCTCTTGCTGGACGT | 9100 |
| rs377007932 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84761937 | ACGTGCAGAGCATGC[A/G]CTCACGTGAACAGCT | 9100 |
| rs377010493 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84741428 | GGACTTCCTCTGTCA[C/G]TGTGTGCTTTGCACG | 9100 |
| rs377011295 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84709141 | GCATTGTTTCTCTCG[A/C/T]GGAGGAGTTTATGGG | 9100 |
| rs377070822 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779824 | TTAATTCTGCTGTCT[A/G]CTCTTCTCTAATGCT | 9100 |
| rs377162555 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84711107 | GCCACTTTGAAGAGC[C/T]GTCATGTCGTGTCTT | 9100 |
| rs377188278 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84765431 | TCTTCCATTCCCACT[C/T]GCCACCCCTAGGAAC | 9100 |
| rs377214798 | snp | C/T | 0.000182365 | 0.00954722 | intron-variant | USP10 | GRCh38.p7 | 16:84759993 | ACATATTGGGAGTTA[C/T]GGAGACAGATGACTT | 9100 |
| rs377233979 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84701934 | TCTCATAATTTTCTT[C/T]TTCTTTTTTTTTTTT | 9100 |
| rs377234102 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84750404 | AGAGTGAGACTGTCT[A/C]AAAAAAAAAAAAAAA | 9100 |
| rs377235670 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84776309 | GGGGTGAGGGCCTAG[C/G]GGTGGGGGCCCAGGG | 9100 |
| rs377249564 | snp | A/G | 9.12756e-05 | 0.00675496 | intron-variant | USP10 | GRCh38.p7 | 16:84745678 | AAAGATTGCAGGTAT[A/G]GTTGAAAAGATACAA | 9100 |
| rs377254205 | snp | A/C/T | 0.000165986 | 0.00910854 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84768281 | CAGTCAGACAAGATA[A/C/T]GCACAGTCCAGGATG | 9100 |
| rs377263422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84716933 | CTTAAAATAGAAGTC[C/T]AGAGCCATAGGGACA | 9100 |
| rs377270579 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84702156 | CTGCCTCCCGGGTTC[A/G]AGCGATTCTCCTGCC | 9100 |
| rs377278711 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84728571 | CCTGACCTCGTGATC[C/T]GCCTGCCTCGGCCTC | 9100 |
| rs377289763 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84751418 | GATATTTTGCACTTC[C/T]TCTTCAAACTCTGAA | 9100 |
| rs377318403 | snp | C/G | 1.65919e-05 | 0.00288022 | intron-variant | USP10 | GRCh38.p7 | 16:84772495 | GTGGTGTTAGCTGTT[C/G]CAAGTAAGACAGGGA | 9100 |
| rs377330911 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84713754 | TCACAGGAGAGTCCC[C/T]GGGGACACCTTGGCT | 9100 |
| rs377338382 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84727926 | TGACCATATAATGTC[C/T]TTTCTAGAATTTTCC | 9100 |
| rs377338499 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698747 | ACGCCTGGTGTGCCA[C/G/T]ACTACATCCCACCAA | 9100 |
| rs377391481 | snp | A/G/T | 5.00864e-05 | 0.00500407 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745380 | AGGGCACAGCTACCA[A/G/T]CGGGGTGGAGTTGCA | 9100 |
| rs377396621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84758698 | CAATTTCTGAAATAT[A/G]CTTCTTCACTCTTTC | 9100 |
| rs377470022 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84775611 | GTTGGGTGAGCGCGC[C/T]CCCAGCCGGTGATCC | 9100 |
| rs377474873 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84701744 | TGCATTCATTGTCCC[A/C]GTATTTACGTTTTAT | 9100 |
| rs377480784 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84714973 | CTTGCTCTGTCGCCC[A/G]GGCTGGAGTGCAGTT | 9100 |
| rs377492307 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84738266 | GATGAAACTGTTTTG[A/G]CTCAGAAAAAGATGA | 9100 |
| rs377503171 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84773794 | GAATGCCGGCTAAGT[C/T]AAAGAAGGCATCCTC | 9100 |
| rs377526096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84730137 | CTGCGTCCACTCAGC[A/G]TCCACTCAGTGCTAC | 9100 |
| rs377584670 | snp | C/G | 6.62855e-05 | 0.00575659 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764181 | GAATGGGAACAAGTG[C/G]GCCCCCGGAACAAGA | 9100 |
| rs377621542 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84735509 | TTCCTTTTGGGCCTC[C/G]CATTTCTTTTCTCTT | 9100 |
| rs377637767 | snp | A/G | 0.000165986 | 0.00910854 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744954 | AAAAGCGGCCACCTG[A/G]ATATTACAGCTATTT | 9100 |
| rs377674468 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84711268 | TTAAAAATGTAAGTA[C/T]ACATGTGTTCCCCAG | 9100 |
| rs377711272 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84732929 | GTGTATCCTATGGAA[A/G]TGCATTTTTAAACTA | 9100 |
| rs377729309 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84746517 | GTAGGCAGTTGTAAC[A/T]CAGTGCTAAGTATTT | 9100 |
| rs377737416 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84702303 | CTCAGGTGATCCACC[C/T]GCCTCGGCCTCTCAA | 9100 |
| rs377745152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84716843 | CCTGGTCTAAACTTA[C/T]CCCAGCATAATTCAT | 9100 |
| rs377761325 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84768415 | CTGGTTTGGTGGAAA[G/T]AACACAAAATTAGGA | 9100 |
| rs377761778 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84757189 | GTTCAGTTCGTAACT[A/G]ATCCATTATTCATTT | 9100 |
| rs386385288 | in-del | -/AA | | | intron-variant | USP10 | GRCh38.p7 | 16:84749575 | GAGACCCCATCTTTA[-/AA]AAAAAAAAAAAAATT | 9100 |
| rs386793444 | in-del | CTTTC/G | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698584 | TTTTTCTTTTCTTTT[CTTTC/G]TTTCTTTCTTTCTTT | 9100 |
| rs386793445 | multinucleotide-polymorphism | CAC/TAG | | | intron-variant | USP10 | GRCh38.p7 | 16:84714290 | TAAAATGTGGAATGA[CAC/TAG]TTGTTTAGTAAAATG | 9100 |
| rs386793446 | multinucleotide-polymorphism | CA/TG | | | intron-variant | USP10 | GRCh38.p7 | 16:84732413 | CTCCGTTGTGGAAAT[CA/TG]CTAATTCTTCTCAAT | 9100 |
| rs386793447 | multinucleotide-polymorphism | GCG/TCA | | | intron-variant | USP10 | GRCh38.p7 | 16:84736108 | AGTGGCGAGGGGAGG[GCG/TCA]TGTCACTTCTACAGC | 9100 |
| rs386793448 | in-del | ATT/GTTTGCTGCAACTTA | | | intron-variant | USP10 | GRCh38.p7 | 16:84775294 | TACAGCTGGGCACAG[ATT/GTTTGCTGCAACTTA]GCATAGCGACCAGAT | 9100 |
| rs397694419 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84723158 | AGGGTTTTTTTTTTT[-/T]TGGCCTTTTTTCCCC | 9100 |
| rs397714422 | in-del | -/T | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84765490 | CTTTTTTTTTTTTTT[-/T]AATAAAGATTCCATG | 9100 |
| rs397718999 | in-del | -/TG | | | intron-variant | USP10 | GRCh38.p7 | 16:84765270 | TTGTGTGTGTGTGTG[-/TG]CACATGGCAAGAGCA | 9100 |
| rs397831034 | in-del | -/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84776324 | CGGTGGGGGCCCAGG[-/G]GTGAGGGCCCAGTGG | 9100 |
| rs397831555 | in-del | -/T | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84731786 | AGCTCTTTTTTTTTT[-/T]GTGATAGTCTGTGCT | 9100 |
| rs397854670 | in-del | -/A | | | intron-variant | USP10 | GRCh38.p7 | 16:84771070 | AAAAAAAAAAAAAAA[-/A]GTGTTATCCAAATGA | 9100 |
| rs397854713 | in-del | -/TT | | | intron-variant | USP10 | GRCh38.p7 | 16:84723158 | AGGGTTTTTTTTTTT[-/TT]GGCCTTTTTTCCCCC | 9100 |
| rs397855813 | in-del | -/A | | | intron-variant | USP10 | GRCh38.p7 | 16:84734274 | GTATTAAAAAAAAAA[-/A]TCTTGCTAACTCTTG | 9100 |
| rs397856271 | in-del | -/AA | | | intron-variant | USP10 | GRCh38.p7 | 16:84749588 | TAAAAAAAAAAAAAA[-/AA]TTATACACACACAAA | 9100 |
| rs398030066 | in-del | -/T | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84746173 | GCTGAACCCTTAACA[-/T]TTTTTTTCTCTTCAA | 9100 |
| rs398030067 | in-del | -/T | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84755812 | CCAGCAAGTGACTGA[-/T]TTTTTTTTTTTTTTT | 9100 |
| rs398030068 | in-del | -/AG | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84775900 | AAGAGGTAAAGACTC[-/AG]AGGCATAAAAGATGA | 9100 |
| rs398042267 | in-del | -/G | 0.5 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84728983 | TTTGTATTTTTAGTG[-/G]AGGTGGATTTCACCA | 9100 |
| rs398100343 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84728369 | TTTACTTTTTTTTTT[-/T]CTCGCTGTTGCCCAG | 9100 |
| rs527237915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84757765 | GAGTTGAGGCCCTGG[C/T]TATGCTACCTGGCTC | 9100 |
| rs527242909 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84721404 | ATTGGTCTTCAAGAG[C/T]TTTGATTATGGTACT | 9100 |
| rs527258319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84727731 | AATATTTTTCCAAAC[C/T]CTTTGAGATTTCAGG | 9100 |
| rs527263150 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84765507 | ATAAAGATTCCATGT[A/G]TAAGTGAGACCATGC | 9100 |
| rs527361689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84761601 | AATGCTGCCAACCAG[A/G]GAAGGTCATTACAGA | 9100 |
| rs527388657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84723698 | AAGATGGATCTAACT[C/T]GATTCTTGTACTTTA | 9100 |
| rs527391790 | snp | A/G | | | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719601 | TAGGTGAGTACCACC[A/G]CGGATTGGTTACCTG | 9100 |
| rs527447984 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84719074 | TGGGATTACAGGCAT[A/G]AGCCACCGCGCCCGG | 9100 |
| rs527451852 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84756929 | CTTGGAATAAAAGGG[A/G]TTTTTAAGTGAAGCC | 9100 |
| rs527461404 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84714677 | GTCCAATTTTTAGTT[G/T]TTACTTGTGAATTTA | 9100 |
| rs527481423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84745987 | ATGAATGTATAATGG[A/G]CTTTTTCTGTGATAT | 9100 |
| rs527486913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84765070 | ACAGAGCAAGACTGT[C/T]TTCAAAAAAAAAAAC | 9100 |
| rs527500050 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84770418 | AGGTTTTGGGGAAAA[C/T]AGGATTATATGAAAT | 9100 |
| rs527516870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84710443 | GGGGAAAGAAGTAGG[A/G]CATTTCTTTTGGGGA | 9100 |
| rs527538699 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84712882 | GAGATGATAGGACAC[G/T]TAGCAATGCAGAGAG | 9100 |
| rs527607947 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84742020 | CCTTTGCAGAGGCAC[C/G]TCATCGTGGCTTCCC | 9100 |
| rs527640717 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84743940 | CGTTTGCATGTGTTC[A/G]TGTCAGGGCCATTTT | 9100 |
| rs527679127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84744562 | TTTATTTTCAAAGAG[A/G]AAGTGAGTAATTACT | 9100 |
| rs527680999 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84771594 | CAATACTAGGCCTAG[C/T]GTGGTGGCTCACGCC | 9100 |
| rs527685648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84766634 | CACAGAGGGTCAGCA[C/T]ACTCAAAGATCCCAA | 9100 |
| rs527712507 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718250 | TTTCTGAAGAGTTGC[C/T]TGTGAGTTCATTTAT | 9100 |
| rs527742941 | snp | C/T | 3.32668e-05 | 0.00407827 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744982 | TTTGAAAGATGGTGG[C/T]GATGATAGTATCTCC | 9100 |
| rs527743008 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84771128 | GTACAGAGAATGATA[A/C]AGGGATTGTTATTTG | 9100 |
| rs527757133 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84725278 | TCTTGGCATTTCATA[C/T]GAATGGAAGAAACAA | 9100 |
| rs527760891 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84711002 | ACAAAAATATGAATT[G/T]TGCCCCTCCCTCTGA | 9100 |
| rs527805710 | snp | A/G | 0.029116 | 0.117091 | intron-variant | USP10 | GRCh38.p7 | 16:84770767 | ACAGAGCGAGACTCC[A/G]TCCCCAAAAAAAAAA | 9100 |
| rs527807979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84774923 | CAGGAGCATCACAGC[C/T]TCGGCCGTTGCTCCT | 9100 |
| rs527812892 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84736621 | AAAGAAAGAGAAAAT[C/G]CTCACCATTCTTTAG | 9100 |
| rs527846319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84705232 | TGTGCCTTGTTTTTT[C/T]TGTTTGTTTTTTTTT | 9100 |
| rs527850229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84750199 | GATCCCTTGAGGCCA[A/G]GAGTTCAAGACCAGC | 9100 |
| rs527877024 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84778207 | GCAGTGCCCCACCAC[A/C]GCTCCACGCTCAAGC | 9100 |
| rs527905478 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84749851 | TGGACCTTCTTGGTG[G/T]CAAGGCCATCTCCTC | 9100 |
| rs527911996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84754345 | AAATCTAGGTTGTTC[A/G]TGTCTCTTCTGTATT | 9100 |
| rs527931810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84777857 | TTGTGCCACTGATGG[C/T]GGGCGCAGCTTAGCA | 9100 |
| rs527966257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84753797 | TGTTTAATTGATCCT[A/G]TATTACTGTCTAATG | 9100 |
| rs527970493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84706002 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCCCCC | 9100 |
| rs527971990 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84743329 | TCACCCCCCACAGTC[A/G]GGGGCTGTGATTCTA | 9100 |
| rs528004817 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779410 | GTAGAATAAATCCTG[C/T]ACCAGCAACAACACT | 9100 |
| rs528037849 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84701371 | TTTGTAAGTAGTGTA[G/T]GTCTTTGCGCCAAAA | 9100 |
| rs528053108 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84708970 | AGCAGGCTAATGGCT[A/G]GGTGCATCCAGTTTT | 9100 |
| rs528054434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84747121 | CCGAAATGTTACGCC[A/G]CGCGTGACTGTACGT | 9100 |
| rs528056615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84716105 | ACTTCTGAACTGGGT[A/G]ACTACTATCCCACAG | 9100 |
| rs528073701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84742655 | GCCAAGCGTGCAGGC[C/T]GTCCTGCACTTCGTC | 9100 |
| rs528117351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751151 | TTACAGTTGCCTACG[A/G]TATTCAGTACACAAC | 9100 |
| rs528125475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84711800 | TCTCAGCTCACTGCA[A/G]CCTCTGCCTCCGGGG | 9100 |
| rs528136864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84743030 | CCACATGGAGCCTTC[C/T]GCCCCAGGCACACCC | 9100 |
| rs528164371 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84750745 | TTGTTTTAACAGAAT[A/G]TAAATAATGCTGGGT | 9100 |
| rs528188928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84707703 | TTGAAGTGACTTATC[A/G]GGATCCAGTGTGCAG | 9100 |
| rs528190765 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84712056 | CAGAAACACCTTGCA[C/G]CTGTGCTTCGTTGCC | 9100 |
| rs528197687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84739283 | GTTTTGTTTTGTTTT[A/G]GTTTTTGAGACAAAG | 9100 |
| rs528230761 | in-del | -/AA | 0.00517822 | 0.0506191 | intron-variant | USP10 | GRCh38.p7 | 16:84706399 | TTGAGAGAAAAGTAC[-/AA]AGAGTTCCTATATAC | 9100 |
| rs528247202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84754772 | AGTTGATTTATGTAT[C/T]CTTTGATTGCATAGA | 9100 |
| rs528248781 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84703085 | CCAAATATTAGAAAG[G/T]GTTGGTTGATCCCTG | 9100 |
| rs528261491 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84741167 | TAATTACAATTTAGG[C/T]TTCAATAGAAGCCTT | 9100 |
| rs528308371 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84703622 | ACAATTGTTTGAAAT[G/T]TTGACAGGGCATTTG | 9100 |
| rs528308880 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84758978 | AGGATTATTCCTGAC[C/G]CCAGTCCATCTCCCT | 9100 |
| rs528336986 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84729806 | AAGGAAATTAAGTTG[C/G]AGTTCAAAACAGCCG | 9100 |
| rs528358674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84704251 | AGGTGGCACATTAAA[C/T]GTGGTTGCTGAGGAC | 9100 |
| rs528370041 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84724725 | TCACCATGCCCTGAC[C/T]CCTGTGTGTGTTGTG | 9100 |
| rs528403622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84725422 | TTTCTTTTTTGAGAC[A/G]GAGTTTTGCTCTTGT | 9100 |
| rs528418866 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84762574 | CACACACCTGGAGTC[A/C]CAGCTACTCGGGAGG | 9100 |
| rs528428402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84706609 | GCAGTGGCGCAATCT[C/T]GGCTCACTGCAAGCT | 9100 |
| rs528461190 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84733327 | AGAAAGGATCTTGGG[G/T]GTTATGGCCCAAATG | 9100 |
| rs528484554 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84772206 | ACAGGCGCCCACCAC[C/T]ACGCCTGGCTAATTT | 9100 |
| rs528484559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84755652 | AAAATAATAATTATG[A/G]TTGGGTATGGTGGCA | 9100 |
| rs528484567 | snp | C/G/T | 3.59719e-05 | 0.00424083 | intron-variant | USP10 | GRCh38.p7 | 16:84760149 | TTGTAGTTAGGAAAA[C/G/T]CTGTGTCCTCTTTCC | 9100 |
| rs528496274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84702183 | TGCCTCAGCCTCCCA[A/G]GTAGCTGGGATTACA | 9100 |
| rs528506967 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84711261 | CATGTTTTTAAAAAT[C/G]TAAGTACACATGTGT | 9100 |
| rs528556930 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84754710 | GGTTTCTGTCTGACT[A/G]GTTCATGCTGTCTCA | 9100 |
| rs528572171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84702674 | TGTCACTGAGAATAA[C/T]GGGAGGTGGAAAAAG | 9100 |
| rs528624327 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84702462 | TCCAGTCATTCTGAG[A/C]GTTTTAATAAATTTG | 9100 |
| rs528624820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84763827 | GATCCAGTGACGTTG[C/T]GCCTGTTGGGATTGG | 9100 |
| rs528640812 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84729262 | ATGTTTGAATGGTTA[C/T]CATGCCAGCTTACTT | 9100 |
| rs528702986 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84724782 | CATAGTTGAGTGTGG[A/G]TTGTTGATGCTCAGT | 9100 |
| rs528709196 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84700306 | CGTCCCCTGAGCCAC[C/T]CGGACCCCCTAGTCC | 9100 |
| rs528722765 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719604 | GTGAGTACCACCGCG[C/G]ATTGGTTACCTGCTT | 9100 |
| rs528753375 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84746732 | AGTTTTATAAACAGT[C/G]AACACTTAGGCTGTA | 9100 |
| rs528757442 | snp | A/G | 1.65605e-05 | 0.0028775 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84772559 | GAGATAAGTCGAAGA[A/G]TGACTCTGGAAAAAC | 9100 |
| rs528810052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84767031 | ACCAGCTCTCATGAG[C/T]GGTTTCCCCACTACT | 9100 |
| rs528817351 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84709289 | TGGAAGTGACGTGTT[G/T]ACAGCATGAGACAGT | 9100 |
| rs528860546 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84769845 | GCTGGTAGGGGTGGC[A/G]GTGTGGGGGCAGGGG | 9100 |
| rs528876987 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84705064 | GTGTACAGCCTTATC[A/G]GTTGTCATTCTTCGG | 9100 |
| rs528919815 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84769506 | TAAGAAGAGTCTGGC[C/G]GTGGACCTCGTGGAA | 9100 |
| rs528967891 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84737744 | AAGCTGGCAGTGTCG[C/T]CTGGCTTCCTCATCT | 9100 |
| rs528978592 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84700594 | CCCCAAGAGCTTCCT[A/T]TCTCAGCTTGATTGA | 9100 |
| rs529024845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84721987 | GGCTGGGAGCCATCA[C/T]GCCCAGCCCAGTTTG | 9100 |
| rs529044129 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84748620 | AGAATATTATAGTTT[C/T]GTTTCTAAAATTGCT | 9100 |
| rs529052747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84773203 | AGCCCCAGGTTAAAG[A/G]CATCTTGCTAAAAGC | 9100 |
| rs529055713 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84727241 | TAATTCATGTCATCA[A/G]TGGCATTTCCCTCTT | 9100 |
| rs529082303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84752279 | TTGCTGTCTGAACAG[C/T]TAAGTAGTAAATTAT | 9100 |
| rs529088144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84722432 | TTCATTTCTTGTGGG[C/T]AAAATGTGGTAAGCG | 9100 |
| rs529114066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84748373 | CAGTGGCGCAATCTC[A/G]GCTCACTGCAACCTT | 9100 |
| rs529120492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717951 | GGGATTCGTGATCAC[A/G]TTAGGGTATTTGTGA | 9100 |
| rs529145529 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718294 | GATTGTACTCTGTGA[A/C]CCAAGATAGAGTGCA | 9100 |
| rs529149920 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84776239 | TCCACCTCAGCTCAC[G/T]CCCGATGTTTTAGGA | 9100 |
| rs529185715 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84743570 | AAAAAAAAATTGGCC[C/T]CTTAATGCTAGCCTG | 9100 |
| rs529192380 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84770257 | ACAGCAGATGTTTCA[C/G]GAAGATTTGGGACAG | 9100 |
| rs529208821 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84741668 | TGTTCCCTCTAAGTC[C/T]TGCCTTTTTTCTGCC | 9100 |
| rs529266580 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84716789 | TGAAGATTCTACCTT[C/T]ATATACACCTTACAA | 9100 |
| rs529271387 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | USP10 | GRCh38.p7 | 16:84774472 | CTGAAGTTTTGTTTT[G/T]TTTTTTTTTTGTTTG | 9100 |
| rs529340064 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84720971 | CGATCTCAGCTCACG[G/T]CAACCTCCGCCTGCC | 9100 |
| rs529345367 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84749047 | TGAGGCTTCGATAGA[C/T]AGAACGTAGTTGTTG | 9100 |
| rs529356442 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84715032 | CTCTTGTGCTAAAGC[A/G]ATTCTCCTGCCTCAG | 9100 |
| rs529380746 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84749120 | CATTGAATAACCCTT[G/T]GGATCATATAGGGCT | 9100 |
| rs529384499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84717039 | CAAACTTAAAAGTCC[A/G]TTGAGAATCAGCTGC | 9100 |
| rs529384501 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84728443 | CTCCCCGGTTCAAGC[A/G]ATTCCCCTGCCTCAG | 9100 |
| rs529411832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84777119 | TTAAGAACTGCTGTG[A/G]TTGTGGGGCCTGGGA | 9100 |
| rs529412070 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84721306 | GGGTGTACTGAAGAA[G/T]TCTTCTTCCGTAGAT | 9100 |
| rs529441981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84743421 | CTTGCACGTAACTGG[C/T]CCCTCTCAGCGTCTG | 9100 |
| rs529445198 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84712768 | AGTGCTCTCTTTACC[A/T]CTGTTGTGTAGTTTC | 9100 |
| rs529446119 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84765232 | AGTGAAGCAGATAAA[C/G]ATATTCCCCATCACA | 9100 |
| rs529465290 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84757143 | ATGACAGGTGCTATC[G/T]CTGCTGGGTGTCATC | 9100 |
| rs529507816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84743926 | ATTTATTTAGAGGAC[A/G]TTTGCATGTGTTCAT | 9100 |
| rs529527289 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84756939 | AAGGGATTTTTAAGT[G/T]AAGCCCCTTATATAT | 9100 |
| rs529537171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84709118 | GAGGGAGTGATGAGC[A/G]AAAACAGGCATTGTT | 9100 |
| rs529540115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84761075 | ATAATGCAGCTTTTG[A/G]TATTGGCTTGGAATT | 9100 |
| rs529597938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84754388 | AAAGGTTTATTCTGC[A/G]TTTAACGACGTCGTA | 9100 |
| rs529598501 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84764963 | ATATATATTAGACTT[C/T]ATCTGCATTTAAAAC | 9100 |
| rs529615642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84735984 | TGGGTGTGTGAGTGG[C/T]GAGGGCGTGTCACTT | 9100 |
| rs529633273 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84760572 | GCAGAACCCAGCTTT[C/G]AAGTCAGTTCTCTTA | 9100 |
| rs529635789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84740501 | TTTTGCTGTAAACTG[C/T]AATGTATTTAATTGC | 9100 |
| rs529654948 | in-del | -/AGG | | | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780133 | CTTCGATTGGCAGAA[-/AGG]AGGAGGTTTTCTCCC | 9100 |
| rs529684494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84723712 | TCGATTCTTGTACTT[C/T]AAAGAAATCAGCTTT | 9100 |
| rs529730849 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84763668 | TATGTAAACAAGGAT[C/G]CAGTGGTGGTGCACC | 9100 |
| rs529737225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84757823 | TCTTTGGGAGCCTCA[C/T]TTTCCTTATTGGTGA | 9100 |
| rs529749160 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84715351 | ATAATGGATAGCTAA[A/G]GCATAAGAAACAACT | 9100 |
| rs529774198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84762472 | AAGGCAGGCAGGTCA[C/T]CTGAGGTCAGGAGTT | 9100 |
| rs529803969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84711041 | CTCACTTATTTTAGC[A/G]CCGAGTGGAATGGTG | 9100 |
| rs529809585 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719509 | TGGCCTGAGGATGCT[C/G]TGATTCTAAGGTGTG | 9100 |
| rs529856338 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84739635 | AACTCTTAAATAAAT[A/G]TTATGGAATAGCTAG | 9100 |
| rs529990022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84770728 | AGTGAGCCGAGATAG[C/T]GCCACTGCAGTCCGG | 9100 |
| rs529990167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84765691 | CACAGACAGTTGTTT[C/T]CCTGTCTTGGCTGTT | 9100 |
| rs530001330 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84713973 | TGGGAAGGTGGATGG[C/G]TGCGTCTTGTAGGCT | 9100 |
| rs530012035 | in-del | -/A | | | intron-variant | USP10 | GRCh38.p7 | 16:84715645 | CCCTCCCTTTTTTTT[-/A]TTAAAAAAACAAACA | 9100 |
| rs530051861 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84770450 | TTTGCTATATAGAAA[A/C]TGTCTGCCTTTGTTG | 9100 |
| rs530093088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741283 | CCATAAGGGAAAGAG[C/T]AGATCTAACAATAGC | 9100 |
| rs530108883 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84767131 | CGTAATTAAACCCTG[G/T]ACAGAAAAGCTTTTA | 9100 |
| rs530134937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84709931 | AGAAAGAATTTGGTA[A/G]TCCAAGCTCAGGACT | 9100 |
| rs530168930 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84771622 | GCCTGTAATCTCAGC[A/T]CTTTGGGAGGCTGAG | 9100 |
| rs530186472 | in-del | -/CCAG | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84708419 | TCACGCCACTTCACT[-/CCAG]CCTGGACGAAAGAGT | 9100 |
| rs530231290 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84771175 | TGACAAAAAACCTGG[C/G]TTTATTTAAAAGCAG | 9100 |
| rs530260048 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84706043 | CTCATTCTTTGAAAA[A/G]AACAATTTGTTGTTG | 9100 |
| rs530265548 | in-del | -/ACAGTTAGTG | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84741717 | TTGCCACCAGTTTGC[-/ACAGTTAGTG]ACAGGCCTGCTTTTC | 9100 |
| rs530280759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84727810 | ATTTCCTAAGAATAG[A/G]CATATTCTCTTAAAT | 9100 |
| rs530291189 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84774945 | GTTGCTCCTGTTTCT[G/T]TAGTGAGCTGGCTGC | 9100 |
| rs530307095 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84770937 | TGGGCATGGTGGTGT[A/G]CACATGTAGTCCCAG | 9100 |
| rs530388053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84777755 | TCCACGTGACAACTG[C/T]GACTAGAACCTGGTG | 9100 |
| rs530417929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84739352 | TCTCGGCTCACTGCA[A/G]CCTCCATCCCCCAGG | 9100 |
| rs530428311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84728254 | ACATTTAGTCAGATA[C/T]CATTTTAGTTAAATA | 9100 |
| rs530429140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84723294 | AAGTGTTCTGTGAAG[C/T]TTAATTCACTTACGT | 9100 |
| rs530444727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84712630 | AGGGGCAGATTTGCC[A/G]TCTATAGAAATAGTA | 9100 |
| rs530452114 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84751893 | AATTTGATGTGTAAA[A/G]TATGTGTAAGAATAA | 9100 |
| rs530478152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84712231 | GTCCTTCCTCAGGAG[A/G]CAGTCAGCTGTGTAC | 9100 |
| rs530559104 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84747532 | TATTTTGGGCTTCAT[A/G]TATATTTTTTAAAGC | 9100 |
| rs530598759 | snp | A/C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779244 | GGTTCGTGCACAACA[A/C/T]AGCTTCTGTTGACTC | 9100 |
| rs530642800 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84707215 | AGGCATAATCTTTCA[C/T]ACTGTGACTTCCCCT | 9100 |
| rs530668325 | snp | C/T | | | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84775221 | AACCTATCGGCTCTT[C/T]GCAGGTGAGTAAATT | 9100 |
| rs530681417 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751212 | TAGGCTCTAGCATAT[G/T]GCCCAGGTGTGTAGT | 9100 |
| rs530705981 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84753832 | CTTACTGTATGCCAT[C/G]CACTGTCTAGTTGGA | 9100 |
| rs530724705 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84726275 | AAAGTGGCGTTTCCC[A/G]CAGTTCCGGCGGGAG | 9100 |
| rs530730196 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699306 | AGGGGCCCCTGTTTC[C/T]TAATAATGAATGAAC | 9100 |
| rs530758196 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84759044 | CTGCAGACAAGCTGG[C/G]TCTCATTAGAATAGT | 9100 |
| rs530781125 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84725750 | TAATCCTTTTTAGAT[A/C]CAAGAGATCCTTTTG | 9100 |
| rs530794080 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699643 | CCAGGTACGCTGAGG[A/G]CGGCTCGTGGGCCCC | 9100 |
| rs530798398 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84729038 | CCTGAAGTCAAGTGA[C/T]CTGCTCGCCTCGGCT | 9100 |
| rs530830322 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84756421 | AACATGGTGAAATCC[G/T]GTCTCTCCTAAAAAT | 9100 |
| rs530836060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84721013 | ATTTTCCTGCCTCAG[C/T]CTCTCGAGTAGCCGG | 9100 |
| rs530892516 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84760414 | AAGAGTCCATTGCTT[A/G]GATGATATGGTGCAC | 9100 |
| rs530908745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84734352 | GACTCTCATTGTTTT[A/G]ATTTACATCTCCCAG | 9100 |
| rs530959311 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84732008 | ACTGTTACTGTCAAT[A/T]CATAATTTCTTTGTT | 9100 |
| rs530966520 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84702327 | CTCTCAAAGTGCTGG[A/G]ATTATAGGCGTGAGC | 9100 |
| rs530969564 | snp | G/T | 0.000798403 | 0.0199641 | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780340 | GAGAGGGATGTCACG[G/T]GCAAGGGTGCCCGTG | 9100 |
| rs530983465 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84729319 | TTCAAAATGTGCATT[C/G]CAATTCTAAGAAATT | 9100 |
| rs531001101 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698066 | CCCCCAGTTTCTATC[C/T]AAGTGCAGATATCGC | 9100 |
| rs531017152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84756122 | CCAACACCCCTTCAG[C/T]TTAGCCTGTACAGTG | 9100 |
| rs531027465 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84731284 | GCTCCCGGCCTCTAC[-/T]TTTTTTTTTTTTTTA | 9100 |
| rs531045494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84716147 | GAGCTGGCCAGTTCG[C/T]TACTGTCCCACATGA | 9100 |
| rs531049670 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717198 | TTCGGGAGCTTCAGA[A/G]GGTCTGTGAAGTTCT | 9100 |
| rs531145056 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84773162 | TCAGGTCACGGGCTC[C/G]GCACTTTTTGAAAGC | 9100 |
| rs531199725 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84763854 | TTGGTTGCCATGGAT[C/G]CAGTGACGTTGCACC | 9100 |
| rs531205690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84768939 | GTGGAGTCCTTGTCA[A/G]CTCAGTTGGGCGAGA | 9100 |
| rs531207579 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84700792 | GCACCCTGCCTGAAC[A/T]GTAGCTAAAGCTTGG | 9100 |
| rs531213484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84765504 | TTAATAAAGATTCCA[C/T]GTATAAGTGAGACCA | 9100 |
| rs531228034 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84700311 | CCTGAGCCACCCGGA[-/C]CCCCTAGTCCCGGGG | 9100 |
| rs531234087 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84730448 | TTATAATAAAAACAC[A/G]CTTAAAATCTATAAC | 9100 |
| rs531248807 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84727327 | ACCCAAACACCTACA[A/G]TTTTCCCCCCTCATG | 9100 |
| rs531266738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84743052 | GGCACACCCGTTTCA[A/G]TCTGGGGAGCCTTGA | 9100 |
| rs531283929 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84735294 | ACATCACACTGATGT[A/G]ACCATACGTTTTAGT | 9100 |
| rs531298736 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84739047 | CTGCTTACCTTACCC[C/T]TTTTCTTCCTAAACC | 9100 |
| rs531307861 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84722489 | AGGCTTTTTCAAAGC[A/G]GCCATGCCGTTTTCT | 9100 |
| rs531312530 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84732312 | AGGAACCACACTCTG[C/G]TTACCATTTTTATAC | 9100 |
| rs531313256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84726816 | CTTGTACTTTGCTCC[C/T]CCGAATCGCAGGCAT | 9100 |
| rs531348845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84761137 | AGGGATGCAGAAATG[A/G]AATGAAGTGCGCCCT | 9100 |
| rs531367687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718318 | GAGTGCAGTGGTGCA[A/G]TCATGGCTCACTGCA | 9100 |
| rs531375551 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84752450 | AGTTGCCTGCCCTCT[A/C]TCCTTGGTGGCCCGC | 9100 |
| rs531401769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84773931 | TTTTATATCCGCTGC[C/T]ACCTCCAATACATTA | 9100 |
| rs531414185 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84773815 | AGGCATCCTCGGCCT[C/G]TGCTCCTGCATCTTC | 9100 |
| rs531428508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84714047 | GGCTTTTCCTGGGCA[C/T]CAGAATAGTAAGGTT | 9100 |
| rs531435016 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84749078 | ACAGTTTCAGGAGTC[A/T]CGTGAGATAGTAGAG | 9100 |
| rs531482402 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84768713 | AGGGTACAACTGTCA[-/G]TTAGATTAGTTAGGA | 9100 |
| rs531517811 | in-del | -/AACTCTAT | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84772893 | AGGCAAAAATAACTA[-/AACTCTAT]AATCTTACTAGATTA | 9100 |
| rs531538354 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741300 | GATCTAACAATAGCT[G/T]AGGACAAGTAATAAA | 9100 |
| rs531586063 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741637 | CTTCTTGGCCCTTTT[G/T]CTCCATTCTTTACTC | 9100 |
| rs531597703 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84728580 | GTGATCCGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 9100 |
| rs531604464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84770748 | CTGCAGTCCGGCCTG[A/G]GCGACAGAGCGAGAC | 9100 |
| rs531634536 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84766346 | TGGAGTGTCCACGGC[A/G]GCTGGGTGGTCAGTT | 9100 |
| rs531659154 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84776740 | ACACACACCCCTCCC[C/T]GACTCTGCAACCTGC | 9100 |
| rs531667335 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84711415 | TGTCCCAGAGAACTG[A/G]AACTTTATAATTCAT | 9100 |
| rs531742648 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84744483 | GTTGTTTCATTTTCC[A/G]CAAATTGTTCAGCGT | 9100 |
| rs531780769 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84730734 | TTACTGGATTGACCA[C/G]CTCTAAAAACTTTAG | 9100 |
| rs531783315 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84763463 | CATACATACGCATAC[A/T]TTTTCCCTGAATGAT | 9100 |
| rs531804895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84740540 | TTTGACTAGTGAATT[A/G]GTTTTAAAGCGTATC | 9100 |
| rs531826663 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84709316 | CAGTGGGGACAGCAT[G/T]TGTGGTGGACCTTTG | 9100 |
| rs531838986 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84749840 | CGGGTTCTACTTGGA[C/G]CTTCTTGGTGGCAAG | 9100 |
| rs531861071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84740193 | TTCTGCTAGAAGTAA[C/T]GGCATGCAAAGTTGT | 9100 |
| rs531862395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84705137 | TCTCCTTAAGCCTGT[A/G]CTCTATGGCTCAGGA | 9100 |
| rs531863060 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84774506 | GTTTTTTTCTTGCTC[C/T]GTCACCCAGGCTGGA | 9100 |
| rs531891677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84753613 | AGGGCGCGAACCCCC[A/G]TCTTCCTGGTTTGTG | 9100 |
| rs531897535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84757192 | CAGTTCGTAACTGAT[C/T]CATTATTCATTTATT | 9100 |
| rs531913317 | snp | C/T | 4.97715e-05 | 0.00498831 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744804 | GTATCACTAAAGAAG[C/T]AAGCTATGGCTCCAT | 9100 |
| rs531920128 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84700438 | GGGTGTGGAGTGGGG[A/C]CCTCCCCGCCGCGCC | 9100 |
| rs531995930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84736462 | GGCATCAGGAGAAAC[A/G]AATTCAGGTGAAAGG | 9100 |
| rs532027505 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84746612 | TGCTTCACCTGTATA[G/T]AGCACTCACCGTGAA | 9100 |
| rs532040253 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84710544 | GGGAAGGTCATTTAG[G/T]GACATATTCCCTTTA | 9100 |
| rs532053918 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84719143 | ATTAACTTGTTAATG[A/G]TCAGTAAACCCTTAA | 9100 |
| rs532061194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84731750 | GTAATTAATTTCCGC[A/G]AACACTTTCATGATC | 9100 |
| rs532075542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84742168 | TACAACAAGTAATAA[C/T]CACATCAAGGTGAAT | 9100 |
| rs532080874 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84756966 | ATATTGAGGAAAGGG[C/G]TCAACCTCTTGAGTC | 9100 |
| rs532096881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84754439 | CTGTCAAAGGCTTGA[A/G]GGAAAGCTTGGTGGA | 9100 |
| rs532099704 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84734941 | GGCAGTGCATCTCCC[C/G]TGGTTCCGAGTGTGC | 9100 |
| rs532143383 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84777729 | GAGGCCTCCTGCTGT[A/C]ATTTAGCCCCTCCAC | 9100 |
| rs532169956 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84707178 | TACTTTGCCAGACTG[A/C/G]TTTTCTGGAAGAGAC | 9100 |
| rs532202902 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84778339 | ACCTTGTTTTCTCAT[A/T]TAATATACCATAAGC | 9100 |
| rs532221321 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84758897 | CAGCTTCCGTGGGCC[A/G]TCTAGCTCTCCATTT | 9100 |
| rs532233452 | snp | A/C | | | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780008 | CTGCAGAATTAAAAT[A/C]TGCCCTTCGATCAGC | 9100 |
| rs532244252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84711441 | TTCATCCTGAAGCCT[A/G]GTTGTCAACATCTCT | 9100 |
| rs532261984 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84742518 | AGTCCTCTCTACTGC[A/C]TGTACTGCAGTGAGC | 9100 |
| rs532289402 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84726699 | TTGAAAGCCCGGGAT[A/G]GAGGCCGGATGGGAT | 9100 |
| rs532335868 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84721518 | CCCATTTTAAGTTTG[C/T]AGTTCGAGGTTTTTT | 9100 |
| rs532343164 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84756684 | GATATAAAAATACTA[C/T]GGCAAAGCCTTGTTG | 9100 |
| rs532356996 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84713532 | CTCCTTGAGGCCCCA[A/G]TGTAAGCTCCGTGAG | 9100 |
| rs532357316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84762517 | CCGACATGGTGAAAC[C/T]CCGTCTCTACTAAAA | 9100 |
| rs532378908 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84763798 | CGTTGCACCTGTTGC[A/G]ATTGGTTGCCGTGGA | 9100 |
| rs532399417 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84734382 | GATTACAAACAGCTG[G/T]GTACTATTTCATTCT | 9100 |
| rs532412774 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP10 | GRCh38.p7 | 16:84769961 | TTCCAGAAAGAAGGC[A/G]GGCCAGGTGTGGTGG | 9100 |
| rs532415080 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84706121 | TCCTGGCCTCAAGGG[A/T]TCCCTTCTGCTTCAG | 9100 |
| rs532420182 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84762021 | ATGCTTCAAACAGAA[C/G]AATTTGCAGGGCCTT | 9100 |
| rs532425390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84732745 | GAGCTACTGCGCCAG[A/G]CCTCAATGACTTGTT | 9100 |
| rs532467428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84729492 | TATTTGTATTGACAC[A/G]TAGGAAAAAGATACA | 9100 |
| rs532471246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84771095 | AAATGAATATGGGAA[A/G]CATCAAAGACTTTGT | 9100 |
| rs532483079 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84758629 | AAGGGATTTTAAATG[C/G]TGTCCCAGAGTAGAG | 9100 |
| rs532487937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84733218 | AGCTTTATCAGTTTC[A/G]TAGTGTTCTTTGACA | 9100 |
| rs532529786 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741630 | GTGACTGCTTCTTGG[A/C]CCTTTTTCTCCATTC | 9100 |
| rs532550299 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779107 | GCGCTGTGTGTGCGC[C/T]CAGTGCCCGCTTCGT | 9100 |
| rs532553287 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84710863 | AGGTTGCAGGTCGTC[C/T]GCATGGGTTTGTGTA | 9100 |
| rs532594342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84737880 | TCCAGCCTTTCCAGC[C/T]TCTCCACCCTCAGTC | 9100 |
| rs532608026 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84728748 | ATATGCAAAAATTAC[C/T]TTTTTTCCTCCCAAT | 9100 |
| rs532614543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84706546 | TATATATTTTTATAT[A/G]TATATATTTTTTGAG | 9100 |
| rs532664099 | in-del | -/TGTT | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84742210 | ACCTCAAGCACTGCC[-/TGTT]TTAGATGTTCCTAAA | 9100 |
| rs532680358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84767890 | ACAAACAAGTGAACA[A/G]AGGTCTCTGGTTTTC | 9100 |
| rs532697544 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719197 | TAAAGACATCTGGAT[A/G]TTGTTCATCAACTTT | 9100 |
| rs532698191 | in-del | -/AAAA | 0.999907 | 0.000944823 | intron-variant | USP10 | GRCh38.p7 | 16:84727459 | AGTGTTAGCTTTAAA[-/AAAA]CAAACAAACAAACAA | 9100 |
| rs532770590 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84703967 | CTGTTACGTGGAACT[C/G]ATAGGATTTAAGCAG | 9100 |
| rs532781593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84740132 | TATTGTGTTTTTTTC[A/G]TTAAATGAAGATGAT | 9100 |
| rs532808320 | snp | C/T | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699510 | GCGTGGCCCAGGCGC[C/T]CAGGCAGGACTTGGG | 9100 |
| rs532813437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84708974 | GGCTAATGGCTGGGT[A/G]CATCCAGTTTTAGGG | 9100 |
| rs532814120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84744418 | CTTAGCTAGAAAGAT[A/G]AGTACAGGCTTCTGC | 9100 |
| rs532823191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84775402 | CTCTGCGTAGATGAC[A/G]GATTATCATCTTGGC | 9100 |
| rs532838275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84735878 | ACATAATCGGATGGA[A/G]TTGTTTTCCCCAATC | 9100 |
| rs532877407 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84721692 | TGCCACCAAGTCTGG[C/G]TTTGTTTTGTTTTGT | 9100 |
| rs532893536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84776139 | GGGAGGTGGGATCCC[C/T]GTTTTATAAAAGAAT | 9100 |
| rs532945029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751923 | ATCATAGCTTATGAT[A/G]ACATAAAAGTTTACG | 9100 |
| rs532951654 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84775877 | ATCCTTCTTTCTCTT[C/T]TATAGCGTCATCTTT | 9100 |
| rs532989186 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84770539 | GCACTTTGGGAGGCC[A/G]AGGCGGGTGGATCAC | 9100 |
| rs533011585 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84773181 | CTTTTTGAAAGCAAT[A/T]TTAAAGAGCCCCAGG | 9100 |
| rs533065791 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84722407 | ACAAGTGTCTGTGTG[G/T]ACATAGGTTTTCATT | 9100 |
| rs533082591 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84721883 | TTTGTGTTTTCATAG[A/C]GACAGGGTTTCACCG | 9100 |
| rs533108133 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699703 | TCCGGGGGCCCAGGT[A/G]GCCCCCAGTAGGTGA | 9100 |
| rs533118326 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84771793 | GAATCGTTTGAACCC[A/G]GGAGACGGATGTTGC | 9100 |
| rs533122503 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84747753 | TGTATTTTTAGTAGA[A/T]ATGGGGTTTCACCAT | 9100 |
| rs533123402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84755194 | TCATTTCCTTCCAGT[A/G]TCAGTGCTAAACAGG | 9100 |
| rs533127464 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84747792 | GGCTGGCCTCAAACT[C/G]CTGACCTCAAGTGAT | 9100 |
| rs533137193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84749095 | GTGAGATAGTAGAGC[A/G]ATAGAGTCACATTGA | 9100 |
| rs533180127 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84748712 | AAAAGCTTCATTTAA[A/T]ATGTTTTAGAACATT | 9100 |
| rs533195942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84721396 | CTGTGGCCATTGGTC[C/T]TCAAGAGCTTTGATT | 9100 |
| rs533198659 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84752607 | AGAAATTTGGAAGTG[A/G]TATTAGTTCTGGCTT | 9100 |
| rs533247250 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84751951 | ACGATGCTGGTATTG[C/G]CTTTGAGTTGATAAA | 9100 |
| rs533260271 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717362 | TTAAATGAAATATGT[G/T]GATTAAATGCCTTTA | 9100 |
| rs533317847 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84726555 | ATGCTTCAGGGAGGA[A/G]GGTGTCTTTTGTTCC | 9100 |
| rs533328357 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84720957 | GGAGTGCAGTGGCGC[G/T]ATCTCAGCTCACGGC | 9100 |
| rs533345824 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84729720 | TTTTAAAAGCTCATG[C/T]ATTTAAGGATTAAAA | 9100 |
| rs533375706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84712277 | CCTGTCCTGAGAGTA[A/G]CGGAAGGAAGACATG | 9100 |
| rs533401647 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84725336 | CTTAGTATAATGTTT[A/T]CAAAGTCATCCTGTT | 9100 |
| rs533453824 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84746656 | ACTGGAGTGGCTCTG[C/G]ATGGGTCAGTGATGA | 9100 |
| rs533455607 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84752407 | CAATGGCAATGACTT[G/T]GGAATGCAGGTCAAG | 9100 |
| rs533507672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84749218 | AAAAGTGGTAAAACA[C/T]ACTCAGTTTGTTACA | 9100 |
| rs533514641 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84747124 | AAATGTTACGCCGCG[C/T]GTGACTGTACGTACC | 9100 |
| rs533520741 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84777181 | GTTCTCAGCGCTCCT[G/T]TCAGGGGGGCTTGCA | 9100 |
| rs533540537 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84715618 | TTGCTTACCCCATTT[A/T]TGTGTTAGGGTGCCC | 9100 |
| rs533580902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84760451 | CTGCTCTCAGTACTT[C/T]ACATATATTAACTTA | 9100 |
| rs533586031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84713755 | CACAGGAGAGTCCCC[A/G]GGGACACCTTGGCTC | 9100 |
| rs533630543 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84743401 | TCCAGCCTCCTGCAC[A/G]CTCACTTGCACGTAA | 9100 |
| rs533678079 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84761194 | TGAATAGTCAACAAG[A/G]GAAGCACAAAGATAC | 9100 |
| rs533682323 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84756641 | AGGCTTTGAGTCTTA[A/T]GGTTAGGTTTAAAAA | 9100 |
| rs533709610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84710044 | GGAGACCGAAGTAGA[C/T]GGATCACTTGAGGTA | 9100 |
| rs533711849 | snp | C/G | 1.65726e-05 | 0.00287855 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764186 | GGAACAAGTGGGCCC[C/G]CGGAACAAGACTTCC | 9100 |
| rs533747374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84737201 | TCAGAACATGACCTT[C/T]CTATAGCCACGGGCC | 9100 |
| rs533778691 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84705807 | TCACTGCAGCCTCTA[C/G]CTCCCAGATTCAAGC | 9100 |
| rs533780305 | snp | C/T | 3.31669e-05 | 0.00407215 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744768 | TTCTCGGTTGTACAG[C/T]TTCCAAAATAACCCC | 9100 |
| rs533840876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84701121 | GAGTAAAATCATAAC[C/T]CTTCATGAGCAATTG | 9100 |
| rs533845715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84740777 | GGCAGCTGGCATCTG[C/T]TGTTCTTGCAGTTCA | 9100 |
| rs533855040 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84727614 | ATCCATTTGCTTAAT[A/C]ATTTGTGTGTGCTGG | 9100 |
| rs533864275 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84752478 | CGCCTTCCTCATTTT[A/T]ATTCTTTTAGCCTCC | 9100 |
| rs533866187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84712009 | ACAGGCATGAGCCAC[C/T]GCGCCCGGTGGCTTT | 9100 |
| rs533909614 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84741103 | CTTTGAGAGTTAGAG[G/T]TTTGGATTCCCTGTT | 9100 |
| rs533924933 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84714361 | GGCTCTGGCATCCAG[C/G]CTGGAGTGAGTGGCA | 9100 |
| rs533939401 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84740237 | TTTAATGAATTGTTG[A/C]CTTAATTAAATGGTA | 9100 |
| rs533947405 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84727431 | AGGTTTTCCTCATAA[C/T]CTCACAATTTTCAGT | 9100 |
| rs533978228 | in-del | -/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84774637 | ACCACGCCCGGGTAA[-/T]TTTTTTGTATTTTTA | 9100 |
| rs533997645 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84736029 | GTGAGTGGCGAGGGC[A/G]TGTCACTTGGACCTG | 9100 |
| rs534012843 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84778559 | GCCACATCCAAGGGC[A/T]TGAGCCAGGTCTGTA | 9100 |
| rs534059967 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84765942 | CTTGTACCATCTCCA[A/G]GAAGGTTTACCCATC | 9100 |
| rs534120620 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84764396 | GCTCCCCTGCCTGCT[C/G]TTCTCTTGCACTTCC | 9100 |
| rs534150080 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84713328 | GTTTGCTCCCCTACT[G/T]TCAGTGAGTCTCTGT | 9100 |
| rs534194496 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84735538 | TTTCTTTTGTTTTTT[A/T]AATTGAAAAAATGCA | 9100 |
| rs534241673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84722159 | ACTATAGGCTAAGAA[A/G]GTTTGCCTTTTCTAG | 9100 |
| rs534244515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84702241 | TTTTGTATTTTTATT[A/G]AAGACGGGTTTCACC | 9100 |
| rs534317768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84738626 | ACAGAATGCTTTCTT[C/T]TGGGTGTCAACGTGA | 9100 |
| rs534365279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84772458 | TCACCTCTCAGAGGA[C/T]GTCTTTGAGCGGAAG | 9100 |
| rs534369948 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84757328 | GAAGAGCTAGCAGAA[A/G]TTATTCCCTACGCTT | 9100 |
| rs534375580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84726501 | AGTGGCCTCCACACA[C/T]CTCCAGAAGGTAAAC | 9100 |
| rs534428001 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84700483 | GCCCGGGGGCTCCGG[C/G]AGTCCCCTGGAGCGC | 9100 |
| rs534447840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84726863 | CCCTGGGCATTTCCT[A/G]TGCAACCACAGGACG | 9100 |
| rs534456504 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84770180 | ATAAAAAGGATGCTG[C/T]CAGCCGTTCTGGGTG | 9100 |
| rs534477810 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84703340 | AGTGAAATCTCCACA[A/G]TAATGCTTCCTACAC | 9100 |
| rs534491251 | in-del | -/C | 0.00755907 | 0.0610114 | intron-variant | USP10 | GRCh38.p7 | 16:84777735 | CCTGCTGTCATTTAG[-/C]CCCCTCCACGTGACA | 9100 |
| rs534501660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84729518 | ATACATGTAGTTTAT[C/T]TGCCATGAGCATATG | 9100 |
| rs534538427 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698333 | CAACTCTTCAGAATG[C/T]ATCTCCTCACAATAA | 9100 |
| rs534540707 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84741618 | CTGCCCTTTTCAGTG[A/G]CTGCTTCTTGGCCCT | 9100 |
| rs534563369 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84778026 | ATGACATCTTCTACA[G/T]ATTTTTTGTTTTAGG | 9100 |
| rs534651232 | in-del | -/AAAC | 0.0268243 | 0.112661 | intron-variant | USP10 | GRCh38.p7 | 16:84727463 | TAGCTTTAAAAAAAC[-/AAAC]AAACAAACAAACAAA | 9100 |
| rs534665636 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84771386 | TGTAGTCCCAGCTAC[A/T]TGGGAGGCTGAGGTG | 9100 |
| rs534681747 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84727936 | ATGTCCTTTCTAGAA[A/T]TTTCCCTTCCAGCAC | 9100 |
| rs534686618 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779959 | ATGCGAATGCCTTTT[C/T]GGGTAACTGAAATTC | 9100 |
| rs534702523 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84755287 | AAGACCTTTCCTTCC[A/G]TATCGTCAAGAAAAC | 9100 |
| rs534715342 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84751069 | GTCAACAACAGACCG[C/T]ATGTACGACAGTGGT | 9100 |
| rs534734914 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84729172 | TTGAATGATGCATAT[C/G]ATTTTGTTAAATACA | 9100 |
| rs534742904 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84723421 | AATGAAAGATGTACT[C/T]CTAGCTGGAACATCT | 9100 |
| rs534768349 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84750453 | TTGTGTTTGAAAGTA[G/T]TTGCAAAACGCGACA | 9100 |
| rs534778009 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84703269 | GGGTAATTAATTTGA[A/G]GCTATTAGTTTTGCC | 9100 |
| rs534787607 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751059 | TGATGTTTCAGTCAA[A/C]AACAGACCGCATGTA | 9100 |
| rs534800444 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84723824 | TGTAATCACCTCCAC[A/C]ATCAAGACACCAGTT | 9100 |
| rs534803648 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84720251 | GATGTGCGTTCCTTC[C/T]TGGCGGGTGGCCTCC | 9100 |
| rs534806382 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84713596 | GGCCCCTAGTCCTAG[-/A]AATGTGGTGAGTGCT | 9100 |
| rs534810817 | snp | A/G | 1.6577e-05 | 0.00287893 | missense, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779039 | AACCAACTGCTGAAC[A/G]CACAGCCTACCTCCT | 9100 |
| rs534821528 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84752463 | CTATCCTTGGTGGCC[C/T]GCCTTCCTCATTTTT | 9100 |
| rs534832765 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84754948 | GAGTTCGAGACCAGC[C/G]TGGCCAATGTGGCAA | 9100 |
| rs534832812 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84759590 | CCTATAATTCTGTCT[G/T]TTTTTAAAAATAGAC | 9100 |
| rs534892221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84759178 | TTCGTAGATCCTTAT[A/G]TGGACATCACAGGAC | 9100 |
| rs534942008 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84770750 | GCAGTCCGGCCTGGG[C/T]GACAGAGCGAGACTC | 9100 |
| rs535013294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84715771 | TGGTTTAATTCAGCC[A/G]TTTAGTTACAGTTTT | 9100 |
| rs535020131 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84742256 | ACTCCTTCACCCTGC[A/C]CTTAGCAATTCAGTG | 9100 |
| rs535028102 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84769490 | ACTTCAGTGAATGAG[C/T]TAAGAAGAGTCTGGC | 9100 |
| rs535039158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84738120 | TGGATGGGTGAAGAG[A/G]TCCCTTCTCTGAATT | 9100 |
| rs535056513 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779423 | TGCACCAGCAACAAC[A/G]CTTGTAAATTTGTGA | 9100 |
| rs535089220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84715874 | CAGGGCTAGTTTCCC[C/T]CACGATGGCGGAATG | 9100 |
| rs535113191 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84738748 | GTTTGTCATAATTCT[C/G]TGGGAAGAGAACTTA | 9100 |
| rs535113573 | snp | C/T | 4.39957e-05 | 0.00468998 | intron-variant | USP10 | GRCh38.p7 | 16:84760302 | CTCTGTTGTCACTAG[C/T]ATCAAGTGTTGCCTT | 9100 |
| rs535183853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84721528 | GTTTGCAGTTCGAGG[C/T]TTTTTGTCTTTGTTT | 9100 |
| rs535229239 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP10 | GRCh38.p7 | 16:84746373 | TTAACTAAGATGGAT[A/G]TGTGTTCCGAGATGT | 9100 |
| rs535252669 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84715501 | TCCGCCTCCCAAAGT[C/G]CTGGGATTACAGGCA | 9100 |
| rs535289940 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84763227 | CTACGATAACTTACA[C/G]CATCGAGAAGGTTAT | 9100 |
| rs535297759 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84744195 | AATCACGTTAACTAC[A/G]GAAGCTGATTTAACC | 9100 |
| rs535353880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84767228 | AGAAACTAGGTCACC[A/G]AGACTGCAGAAATAG | 9100 |
| rs535371889 | in-del | -/TTG | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84734595 | TGGGGTTGGGTTTTT[-/TTG]TTGTTGTTGTTGTTG | 9100 |
| rs535382022 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84772424 | AAGCCATGAAGTCCT[A/G]CCACAGGACTCTTGG | 9100 |
| rs535391603 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84740592 | ATGTAAGATTTAGTT[A/T]AGGAAATGGTTGTTG | 9100 |
| rs535452137 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84755921 | ACACTAAACAAAAAA[A/T]AACCTGCTCATCTGT | 9100 |
| rs535572058 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84763923 | CTGTTGCGATTGGCC[G/T]TGGATCCAGTGACGT | 9100 |
| rs535572879 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84712358 | GAGCCGGAAGCAGCC[C/G]CTGGCCTGGCTGCTC | 9100 |
| rs535624049 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84746769 | TGATTTACAAATTTT[C/T]CCTCAATAAGAAATT | 9100 |
| rs535668611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84704021 | GGAGAAAAGGATTAC[A/G]AAGCTTAATGATTGC | 9100 |
| rs535711367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84744612 | ACTGGGTTCTTAACT[A/G]ATAGTTTTCTTTCTA | 9100 |
| rs535732283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84735323 | GTTGCTACAGGTTTT[C/T]TCAAGTGTGTACACA | 9100 |
| rs535735057 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84713660 | AGACATACCACAGTG[C/G]ACATATTCAGAAGCC | 9100 |
| rs535791280 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84763279 | TCCCGAACCTCTGCC[A/G]TTTTCCTTTAACTTT | 9100 |
| rs535792184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84730582 | CTTGAGGGTGTTTGC[C/T]GCTGACTCATGCTGA | 9100 |
| rs535803214 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84749910 | CCATTGGCTGTTTTT[C/G]AAGTGTGAACTGTTA | 9100 |
| rs535806383 | in-del | -/AT | | | intron-variant | USP10 | GRCh38.p7 | 16:84706916 | GAGAAGGAGAAACAT[-/AT]TTATTACGAGATACT | 9100 |
| rs535814191 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699390 | GTAGCACTTGCTGAG[G/T]GTTTGCTACTTGCCA | 9100 |
| rs535821085 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84720764 | TTTTTTGTATTTTTT[A/C]ATAGAGACGGGGTTT | 9100 |
| rs535826254 | in-del | -/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84752326 | GAAAAGAAGGCTTCT[-/G]GGGGAAAGTTTGTTA | 9100 |
| rs535844797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84714320 | ATGTTTTTCCCACTT[C/T]TTCCTCTTTTTTAGA | 9100 |
| rs535850758 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84769996 | CGCCCTTAGTCCCAG[C/G]ACTTTGGGAGGCTGA | 9100 |
| rs535857127 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84742728 | AGGCACATGGCGTCC[A/G]TTGTGAGTGTTCCTC | 9100 |
| rs535873153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84712004 | GGGTTACAGGCATGA[A/G]CCACCGCGCCCGGTG | 9100 |
| rs535913648 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84769753 | TTCCATGGGCTGCCT[A/G]GGGAAGACCCTTTTG | 9100 |
| rs535921104 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84739121 | TGGAGTGCAGTGGCA[C/G]TATCTCGGCTCACTG | 9100 |
| rs535924543 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84753367 | AAAGTTGTTGGTTTT[A/C]TCAGACTCTCACATA | 9100 |
| rs535976672 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84773786 | GAAACCTGGAATGCC[A/G]GCTAAGTCAAAGAAG | 9100 |
| rs535989340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84757272 | ACTTAGTCTAATTAA[A/G]CAGATTCCACAGAAT | 9100 |
| rs535990041 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84761930 | TCTGCACACGTGCAG[A/C]GCATGCACTCACGTG | 9100 |
| rs535993672 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84706278 | TGAAAATGAAGTTCA[A/G]TTCTAGAGGTTTTCG | 9100 |
| rs536058969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84706633 | GCAAGCTCCGCCTCC[C/T]GGGTTCACGCCATTC | 9100 |
| rs536066326 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84748501 | TAGAGACCGAGTTTC[A/C]CCATGTTGGCCAGGC | 9100 |
| rs536094464 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84770084 | CTGCACTCCAGCCTG[-/T]TGCGATAGTGAAACC | 9100 |
| rs536135388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84756502 | GGAGGCTGAGGCAGG[A/G]AAATCACTTGAACCC | 9100 |
| rs536137776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84752067 | AACTCCATTTTTCTG[C/T]ATGTCAGCAGATTTC | 9100 |
| rs536139793 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84713473 | CATACCCGCTATCCT[C/G]ACGTGTGTGTCTGGT | 9100 |
| rs536187619 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84775994 | AGCTTCTGTGTCTTC[A/C]CTCCTCTGGTGTGGC | 9100 |
| rs536199573 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84756248 | TACCCGGTGCCTAGG[C/G]AGGGCTCAGCAGGGG | 9100 |
| rs536241501 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84736671 | GGAAGTAGCACACAT[C/G]CCAACCATGACTGAG | 9100 |
| rs536253052 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84729321 | CAAAATGTGCATTGC[A/T]ATTCTAAGAAATTCC | 9100 |
| rs536258299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741172 | ACAATTTAGGCTTCA[A/G]TAGAAGCCTTGAAAA | 9100 |
| rs536259292 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84759847 | TTAGTAAAAGTATAT[A/G]TTGTTTAAAACTGCA | 9100 |
| rs536260134 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84749287 | ACTTTTAAGTGTAGG[C/T]CCACTTATTTTAAGC | 9100 |
| rs536261932 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84741532 | GAGTTCACCCTCCTC[A/C]CTGTGCAGTGGGCAC | 9100 |
| rs536312225 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84732701 | GATTCGCCCATGTCA[C/G]CCTCCCAGAGTGCTG | 9100 |
| rs536329317 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84700537 | TGCTGCCTCTGCCTG[C/G]AGCGAGCCTCAGAGA | 9100 |
| rs536336728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84710564 | TATTCCCTTTATTTT[A/G]AGGGGGAGGCACCTT | 9100 |
| rs536350311 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84728303 | TTGCTATAAATATAT[A/T]GAATAAATTGAATAA | 9100 |
| rs536380536 | in-del | -/C | 0.00200401 | 0.0315909 | intron-variant | USP10 | GRCh38.p7 | 16:84743633 | AAGGCATGTGTCCTT[-/C]CCTTAACTTCAAAAT | 9100 |
| rs536384109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84766662 | CAAATTTGTCTAAGA[A/G]TAACCAGTGGAAAAT | 9100 |
| rs536442245 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84766261 | GCAGCCATGTGACCT[G/T]GAACAAGTCACTTCT | 9100 |
| rs536450639 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84749000 | AAAGTGTAGTTTCTT[C/T]AAAAATATATAATTC | 9100 |
| rs536455403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84761641 | CAGAGTTTTTACTGA[A/G]GGCTGGTCCCATAGG | 9100 |
| rs536506356 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84770818 | GATGCCTGTAATCCC[A/C]GCATTTTCGGAGGCT | 9100 |
| rs536586617 | snp | G/T | 0.000308346 | 0.0124128 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745162 | TGTGCCTGACAGTCC[G/T]TTCCCCGGAGCACTC | 9100 |
| rs536596885 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84707811 | CAGGTGCAGTGAGTG[A/T]CTCACGCCTGTAATC | 9100 |
| rs536603522 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84704990 | CAGCACCTGCTACCG[C/T]CTGCGCTGTAATGGT | 9100 |
| rs536603594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84709559 | CCAGTGAAGAATAGA[C/T]TCACGGGGTCGCAGT | 9100 |
| rs536720218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84762651 | AGCTGAGATTGCACC[A/G]CTGCACTCCAGCCTG | 9100 |
| rs536793761 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84700921 | CACATCTTCTCCCCC[C/T]TCCGCCATTATAATT | 9100 |
| rs536822437 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84725434 | GACGGAGTTTTGCTC[G/T]TGTTACCCGGGCTGG | 9100 |
| rs536839309 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84727410 | TCAAACATAAGGAGA[G/T]GGTAAAGGTTTTCCT | 9100 |
| rs536852162 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84774366 | GTCGGTGTAAGTGGT[A/G]CTTCTGCGCACAGTA | 9100 |
| rs536893956 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84775040 | AGGGATAGAGTGTTG[G/T]TTTGTTCCTGGTCTG | 9100 |
| rs536956472 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718460 | TTCTAATTTAGTTGC[A/C]TTATAGTTTTTCTTC | 9100 |
| rs536995533 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84703084 | TCCAAATATTAGAAA[C/G]TGTTGGTTGATCCCT | 9100 |
| rs537022473 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84751119 | GCTAAACAATTTCTA[G/T]TGACCAGTGAGTTGT | 9100 |
| rs537031942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84776255 | CCCGATGTTTTAGGA[A/G]GTTTGGCGAGTGGGT | 9100 |
| rs537032359 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84770290 | TGTATGGAAGTATCT[A/G]TAAGGAGCAAATTAC | 9100 |
| rs537055388 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84767530 | CTATTTACCTTGGGA[A/T]TTCCTCTATTTTATT | 9100 |
| rs537088717 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84702964 | TGCCACTGCACTCCA[A/G]CCTGGGCGACAGAGC | 9100 |
| rs537096467 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719301 | AGCTCCCCTCATCCT[A/C]CTGTTTTCTGCTTAG | 9100 |
| rs537099862 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84767349 | AAAGGAAAAAAAAAA[A/T]GAAATGAAAAACCAG | 9100 |
| rs537108145 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84771418 | GAGAATCACCTGAGC[C/G]CAGGAAGTCAAGGCT | 9100 |
| rs537118288 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698528 | TTTGGTTATGTTTTC[C/T]AGCTCTTCTATTTTG | 9100 |
| rs537129240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84746391 | TGTTCCGAGATGTGC[A/G]TGTTAACATCAGAGA | 9100 |
| rs537160145 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84715544 | TCCACCTGGGTGACC[G/T]TACTACTTTATATGA | 9100 |
| rs537172614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84771800 | TTGAACCCGGGAGAC[A/G]GATGTTGCAGTGAGC | 9100 |
| rs537196462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751368 | ATAAATCATGCATAT[A/G]TTTCCCCCCGCTCCT | 9100 |
| rs537219673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84720341 | GAACAGATGGCACTT[A/G]CAAGTTTCTGCCCAT | 9100 |
| rs537233065 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84775305 | ACAGGTTTGCTGCAA[C/T]TTAGCATAGCGACCA | 9100 |
| rs537290944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84720803 | TAGCGGGGATGGTCT[C/T]GATCTCCTGACCTCA | 9100 |
| rs537313096 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84738691 | GTGCAGCTGTCAACT[A/C]CTGAAGGTGTTGGCT | 9100 |
| rs537319818 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84721074 | AATTTTTGTATTTTT[A/G]GTAAAGACGGGGTTT | 9100 |
| rs537333543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84711866 | CTGGGATTACAGGTG[C/T]GTGCCACCATGGCTG | 9100 |
| rs537354811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84716745 | GCAAGGTTGGTAGGC[A/G]GAGACGCCCATTACA | 9100 |
| rs537520090 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84715659 | TTTTAAAAAAACAAA[A/C/G]AAGTAGAGCTCAGCT | 9100 |
| rs537548661 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718042 | AATGATGAGAGAGAG[A/T]TTGGGAGATTACTTG | 9100 |
| rs537583328 | snp | C/T | 0.00010055 | 0.00708976 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744664 | AATTGAGTTTGGTGT[C/T]GATGAAGTCATTGAA | 9100 |
| rs537593932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84746763 | CTACGTTGATTTACA[A/G]ATTTTTCCTCAATAA | 9100 |
| rs537623174 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779644 | TGAGAGAAACTGCTT[A/T]CGTACACATTGCAGA | 9100 |
| rs537646080 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84764370 | TTCTTGGACGTAATG[C/G]TTTGCATCTTGCTCC | 9100 |
| rs537657262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84742352 | AAGAATCCTTTTTCT[A/G]AAGCTATTCACAGCT | 9100 |
| rs537677878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84711534 | GTTGCTCATGGATTC[A/G]TCAGGTGAGGAAATT | 9100 |
| rs537681497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84709620 | CTTGGACTTTTGACT[C/T]GGAGGGTGCCGTGGA | 9100 |
| rs537706063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84769151 | TAGCATTCCTGCAAA[A/G]CGATATTTGAATAAT | 9100 |
| rs537711871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84736700 | AGTCAATAAGCCCCC[A/G]ATGACATAGTGTTGG | 9100 |
| rs537773975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84732039 | GACTTTTGCAAGTAT[A/G]TGTAAATATTATATG | 9100 |
| rs537855055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84743462 | TCTACAAAAAGATTT[C/T]TAGGGGTCCTTTCAA | 9100 |
| rs537886875 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84722048 | AACTACTACCACACT[C/G]CATATATAGAACATT | 9100 |
| rs537918551 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84739900 | TTGCAATGTAGTGAT[C/T]GTGAATAAGAGGTGC | 9100 |
| rs537923496 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84744326 | CAGATTCCACTGGGG[G/T]GTATTTTTAAAATTG | 9100 |
| rs537983823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84770106 | AGTGAAACCGTGTCT[C/T]TAAAACATAAGAAGA | 9100 |
| rs538027092 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant | USP10 | GRCh38.p7 | 16:84704768 | ATCCCATTTTCATCA[G/T]ATGACTTGAGAACCC | 9100 |
| rs538058732 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84762810 | CAGTTTCTCCTTTTC[C/G]TCCTACTCTTGGGAT | 9100 |
| rs538062015 | snp | C/T | 0.000399281 | 0.0141238 | missense, intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84704843 | ATGCCCTGGTTGCCC[C/T]CTCCTGGAATAGGGC | 9100 |
| rs538108132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741083 | AAACTGATGCCAAAC[C/T]TTTTCTTTGAGAGTT | 9100 |
| rs538113431 | snp | A/G | | | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84715890 | CACGATGGCGGAATG[A/G]CCACAGCAGTTTCAG | 9100 |
| rs538125665 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699896 | AGGGGATGTCCGCGG[A/C]CCGGCAGGCGCACGC | 9100 |
| rs538130708 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84710029 | AATCCCAGCACTTTG[A/G]GAGACCGAAGTAGAC | 9100 |
| rs538165625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84776874 | CTGGAGTGCAGTGGC[A/G]CAGTCTCCATTCACT | 9100 |
| rs538188026 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84749776 | CGTATAAGGGATTTT[G/T]AAGTGAAATACATTA | 9100 |
| rs538212978 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84712420 | TATGGTCTGGCTGCC[C/G]CAGTGTCCCCACTGC | 9100 |
| rs538215959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84717073 | TCTTGTGAATGTGCA[C/T]ATTTAGATTCAGTAC | 9100 |
| rs538229490 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84710615 | TTGATTATATTCGTA[G/T]AAAATATTAAGGAAA | 9100 |
| rs538257943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84737697 | TACTGGCAGTGTCAC[C/T]TGCTGGCACTGTCAC | 9100 |
| rs538264188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84708408 | GTGAGACAAGATCAC[A/G]CCACTTCACTCCAGC | 9100 |
| rs538290525 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84706395 | AAAATTGAGAGAAAA[C/G]TACAAAGAGTTCCTA | 9100 |
| rs538305031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84770472 | CCTTTGTTGAGTGAT[C/T]AGAAATTAAGCCTCA | 9100 |
| rs538308909 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84774748 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGTGCC | 9100 |
| rs538332784 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84749989 | CAGTGATTTCCTTTA[C/G]CCCCAAGGGAAGGAT | 9100 |
| rs538373147 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84735378 | CAAGTGAGTAGACAA[A/T]AACTTGAGTTTTCAT | 9100 |
| rs538406317 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84702388 | TTTCATTTTAAAAGA[A/C]TAGTAATGCAAACAA | 9100 |
| rs538442459 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84726210 | ATGCTGTGCTGCAGC[A/G]CCCCCTAGTGCCGTG | 9100 |
| rs538442808 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84743413 | CACACTCACTTGCAC[A/G]TAACTGGCCCCTCTC | 9100 |
| rs538463210 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84749155 | GAGAATGGCATTGTT[G/T]GAAATTTTTTTTGTT | 9100 |
| rs538466623 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84753447 | TCTAGGGGGGATTCT[C/G]ATGTCTGTATTGAGC | 9100 |
| rs538480339 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84702826 | AGTGAGACCCTGTCT[C/G]TACTAAAAATACAAA | 9100 |
| rs538482220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84725989 | GAGGCTTAGCTGTGC[A/G]TCTGTGAATGGGAGA | 9100 |
| rs538495288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84731181 | AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 9100 |
| rs538506585 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84709976 | GCAACTCTGTGTTAA[C/G]ATAGCTGGTTGAGGC | 9100 |
| rs538513615 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84723925 | GATAGAACTGCTTCT[G/T]TTACAGTTTCTTTTT | 9100 |
| rs538518059 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84774702 | GTCTCGATCTCCTGA[C/T]CTCGTGATCGCCCGT | 9100 |
| rs538521462 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84770622 | CTAAAAATACAAAAA[-/G]TTAGCCGGGCATGGT | 9100 |
| rs538524914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84748852 | TTAATGACTGGTAGT[A/G]GAGGAAAGCCTTGCC | 9100 |
| rs538602095 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84715467 | GGGTAATGAGCTAGT[C/G]TTGAGAAGGAATAGG | 9100 |
| rs538613698 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84736827 | GGAGTCTCGCTCTCT[C/T]GCCCAGGCTGGACTG | 9100 |
| rs538613905 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84740133 | ATTGTGTTTTTTTCG[A/T]TAAATGAAGATGATT | 9100 |
| rs538632016 | snp | C/T | 0.000141578 | 0.00841243 | missense, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84778919 | ATCACGGCAACAGTG[C/T]GACGGGCGGCCATTA | 9100 |
| rs538664133 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84711142 | ACGAGATTTCAGTTT[C/G]GCTTGGCATTCATTA | 9100 |
| rs538690027 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84738096 | CTAACAGCTCTCTGC[C/G]TTGTGAAGTGGATGG | 9100 |
| rs538725247 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84759149 | CAAGTTCTTGAATAC[A/C]AACGACTGACTGCTT | 9100 |
| rs538725881 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84732572 | CTGGCTCAGCCTCCC[A/G]AGCAGCCGGGACTAC | 9100 |
| rs538725974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741714 | ATCTTGCCACCAGTT[C/T]GCACAGTTAGTGACA | 9100 |
| rs538726702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84706710 | CACGCCCAGCTAATT[C/T]TTTGTATTTTTAGTA | 9100 |
| rs538755286 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84777912 | ATGCTGCCGGACAGC[C/T]GCCTTCCCGAGGCTG | 9100 |
| rs538770233 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84722803 | TCAAGTGATTTGTCC[G/T]CCTCGGCCTCCCAAA | 9100 |
| rs538775433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84754103 | TCTTTAAGGAGCCTC[C/T]TGTCCAGAGAAGGAG | 9100 |
| rs538815222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84777560 | TGGCTCTCCGAAGTA[C/T]GGGCCCCACAGTCTT | 9100 |
| rs538823591 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84733932 | TTATTTTAAGCTAAC[A/G]TTGTATTCTTTATGC | 9100 |
| rs538829400 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84728450 | GTTCAAGCGATTCCC[C/T]TGCCTCAGCCTCCCG | 9100 |
| rs538837064 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84757955 | ATTGTAGCCATCACC[A/G]TTAGAAGATTCATAG | 9100 |
| rs538844826 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84730095 | AACCCTCCAAAAAAC[A/G]TGCTAGGAAATCCCC | 9100 |
| rs538848629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84762673 | TCCAGCCTGGGTGAC[A/G]GAATGAGACTTTGTC | 9100 |
| rs538969959 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84761655 | AGGGCTGGTCCCATA[G/T]GTACCATCTGCCTGG | 9100 |
| rs538975079 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84705748 | TTTTTTTGAGACAGT[C/G]TTGCTCTGTTGCCCA | 9100 |
| rs539002023 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741468 | TGCTGCTCATGTTGA[A/T]CCAGTGCTTACAAAT | 9100 |
| rs539026551 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84703878 | GCGCACTGAAATTCC[A/C]GTGAATACTAAGCGG | 9100 |
| rs539038398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84754884 | AGTGGCTCACACCTG[C/T]AATCCCAGCACTTTG | 9100 |
| rs539197820 | snp | A/G | | | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719849 | ATCTTTGGAGGGCAT[A/G]TTTCGACAGATCATT | 9100 |
| rs539198519 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84723344 | AAAATATAAGTTTAA[C/G]TGTTATACTTTAAAA | 9100 |
| rs539213038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718496 | GGGTGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 9100 |
| rs539237415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84721042 | GGGAGTACAGGTGCC[C/T]GCCACCATGCCTGAC | 9100 |
| rs539295739 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84717143 | AATTCCTAGGCTGCT[C/G]GCCTGGTGACCTCAC | 9100 |
| rs539302981 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84775566 | GTGACAGTGCTGTGG[A/C]GTTTCCACGACACCT | 9100 |
| rs539306005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84771905 | AGTACATAAATAAGG[C/T]GGTACTAAGTTAGCT | 9100 |
| rs539331829 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717528 | TGCTCAATAAGTGTC[A/G/T]ATTTAGCTTGGTGAC | 9100 |
| rs539338003 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718143 | ATTTTTGAGAAAGTG[C/G]AGTGTTGGTAGTGAA | 9100 |
| rs539347190 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84771306 | CCTGGAATCCCAGCA[C/G]GGTGGGAGACTGAGG | 9100 |
| rs539364359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84775357 | TGTGGCCTTGTGAGT[C/T]GGGGAGTCACGTGAG | 9100 |
| rs539370490 | snp | A/C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779329 | AATACACAAAAACCC[A/C/G]TATTTCTGAAATAAT | 9100 |
| rs539401492 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698598 | TCTTTCTTTCTTTCT[C/T]TCTTTTTTTTTTTTT | 9100 |
| rs539441141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84759645 | AACCAGAAATGGAAT[C/T]GGAGCATTGATGATC | 9100 |
| rs539463333 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698948 | CAGGCTCCCTATTTT[A/G]TGTAACGTGGGAATG | 9100 |
| rs539508678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84763619 | GCATCTTCAAATTTC[A/G]CCAGTTGTCCCAGGG | 9100 |
| rs539536148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84720818 | CGATCTCCTGACCTC[A/G]TGATCTGCCCACCTC | 9100 |
| rs539549336 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84716181 | TAATGTCTCTCCCCC[C/G]TCTCCTTTTCCAGAT | 9100 |
| rs539575234 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84744027 | AGTGCTCTGAAGTGC[A/G]CTTTTATATATAGGA | 9100 |
| rs539597394 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84747984 | GGTGAAACCCCGTCT[C/G]TACTAAAAAAAACCT | 9100 |
| rs539610329 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84735876 | TAACATAATCGGATG[A/G]AGTTGTTTTCCCCAA | 9100 |
| rs539617250 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84711981 | TGCCTCAGCCTCCCA[A/G/T]TGTACTGGGGTTACA | 9100 |
| rs539631577 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780362 | GTGCCCGTGCCCCGG[C/T]TTCTGGCCCTGTGTG | 9100 |
| rs539653570 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84749448 | AAGAGGGAGTAGGGA[A/G]TGATTTAGACATTAA | 9100 |
| rs539661321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84756208 | CTAGGGCAGGACCAC[C/T]TTGCATTCATCTCTG | 9100 |
| rs539732064 | in-del | -/TTGTTG | 0.0282754 | 0.115491 | intron-variant | USP10 | GRCh38.p7 | 16:84744047 | TATATATAGGATTCT[-/TTGTTG]TTGTTGTTGTTGTTG | 9100 |
| rs539757649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84739960 | CAAACAAAAGTGTCT[A/G]TGGTCTGGATGGTCA | 9100 |
| rs539766355 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84730420 | ATCTGTGGAGAAATT[-/A]ATTGACATGAAGTTA | 9100 |
| rs539772599 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84734944 | AGTGCATCTCCCCTG[C/G]TTCCGAGTGTGCTAT | 9100 |
| rs539815876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84710417 | TGGCATCTTAAGCCT[C/T]ATAACTTTGAGGGGA | 9100 |
| rs539854407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84746812 | CTGTAACTTTTTTAC[A/G]TTTTATTTTACTTTT | 9100 |
| rs539915180 | snp | C/G | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699378 | CGTGTGCAACACGTA[C/G]CACTTGCTGAGTGTT | 9100 |
| rs539929580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84748601 | GAGCCACCGCGCCCA[A/G]CTGAGAATATTATAG | 9100 |
| rs539936655 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84748625 | ATTATAGTTTCGTTT[C/G]TAAAATTGCTCCACA | 9100 |
| rs539955052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84776347 | CCCAGTGGGTGAGGC[C/T]CAGAGCCACACTGCA | 9100 |
| rs539967291 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84722533 | GTGTATGAGAATGCT[G/T]CTTCTCTGTCCTCAC | 9100 |
| rs539991812 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84731537 | CCAAGAAAAAGGTGT[A/G]TGTGACAGAAAGTGT | 9100 |
| rs539994244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84752232 | CCAACTCCTGTGACA[A/G]AGATGGACTGGGGGA | 9100 |
| rs540014217 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84775997 | TTCTGTGTCTTCCCT[A/C]CTCTGGTGTGGCCTT | 9100 |
| rs540024736 | snp | G/T | 0.000455788 | 0.0150893 | intron-variant | USP10 | GRCh38.p7 | 16:84700160 | GCCCGAGCCCCGGGC[G/T]GGCGGACGCCGCGGC | 9100 |
| rs540025604 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84739102 | CTTGTGCTGTTGCCC[A/C]GGCTGGAGTGCAGTG | 9100 |
| rs540059578 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84758370 | CTGGCTAATGGTGTT[G/T]AAGGAAGAAAGGCTG | 9100 |
| rs540060096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84707889 | TTTGGGACCAGCCTG[A/G]GCAACGTAGCAAAAC | 9100 |
| rs540090590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84734650 | TTAATGTCAACTGAA[C/T]TGATTTTTTTTTCCT | 9100 |
| rs540095067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84727176 | GCTTTTTAGTCTCCC[A/G]TGTGAACTGAATTGT | 9100 |
| rs540101103 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84755779 | TTCCAGCCTGGGCGG[C/T]AGAGTGAGACTGTCT | 9100 |
| rs540124499 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84703460 | CACATTTTACATGAT[A/G]GAAAGTCTTGGATTC | 9100 |
| rs540127641 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84743925 | AATTTATTTAGAGGA[C/T]GTTTGCATGTGTTCA | 9100 |
| rs540174587 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP10 | GRCh38.p7 | 16:84760020 | ACTTAAATTTGGTAA[A/G]TTCAGTCTTGTTGGG | 9100 |
| rs540188037 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84711156 | TGGCTTGGCATTCAT[G/T]AAGTCCATGATTATG | 9100 |
| rs540244017 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84740452 | TGTAAACATTGTTTC[C/G]CATTTGAATAAACAT | 9100 |
| rs540288107 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84756619 | GTTTCTATGTTAGAA[A/G]GATAGCAGGCTTTGA | 9100 |
| rs540359148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84736834 | CGCTCTCTCGCCCAG[A/G]CTGGACTGCAGGGGC | 9100 |
| rs540394504 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84703760 | TGGCCTGAGAAGTTT[A/G]TGAGCCAGTGGTCGC | 9100 |
| rs540421830 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84732157 | CCAGGAGGGTATTAC[A/C]TTTAGTGGCCATTTA | 9100 |
| rs540447438 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780240 | TAAATGCTCTTCAGT[C/T]GAGTGCCACTGGGGC | 9100 |
| rs540489684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84756056 | TTCCCAGAGTTTCTG[C/T]AGCCCTTGGATTGGG | 9100 |
| rs540505377 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84706544 | TATATATATTTTTAT[A/G]TATATATATTTTTTG | 9100 |
| rs540523047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84764872 | AGAATGTCATCATGA[C/T]TTAGGGGTAGGCAAA | 9100 |
| rs540587525 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84723262 | TTTTTCTTTAGGTCA[A/T]AATAGGTGTTCCTTT | 9100 |
| rs540593831 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84769816 | GCAATTACAGTTTGA[A/C]TTTGCTGGGGTGGGC | 9100 |
| rs540626794 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84743078 | CTTGACGGCCCCAGA[A/G]CATCAGGGAATAGGG | 9100 |
| rs540743169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84720965 | GTGGCGCGATCTCAG[C/T]TCACGGCAACCTCCG | 9100 |
| rs540759078 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84761375 | CTCCCCAAGACCACC[C/G]TGAGGTTGGGTGATT | 9100 |
| rs540769769 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84774943 | CCGTTGCTCCTGTTT[A/C]TTTAGTGAGCTGGCT | 9100 |
| rs540792553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84766010 | TTTCTGAGGCCTTGC[A/G]GCATAACCCCCAGGC | 9100 |
| rs540795980 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84738770 | GAGAACTTACTGCGT[C/T]ACTAGCAGAGAGAAG | 9100 |
| rs540812515 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84765418 | CCTTCGACCGACATC[G/T]TCCATTCCCACTCGC | 9100 |
| rs540827190 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84722358 | AGACATTTTTGTTGT[C/T]CCCACTGTTTGAATC | 9100 |
| rs540832732 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84755690 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAC | 9100 |
| rs540912384 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84743856 | TTCACAATTCTAACT[G/T]TTTCTTTTGGTATTT | 9100 |
| rs540948875 | in-del | -/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84777939 | CTGGTGTCTGCTGCT[-/G]GGCCAGGCAGACCTG | 9100 |
| rs540969432 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84753902 | AGATCAGAAAGGAAC[A/G]GATGGCAGCTGTTTG | 9100 |
| rs540973751 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84744357 | GCAAAATATTACTTG[A/C]TTTTTATTACAAATT | 9100 |
| rs540974940 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84715904 | GGCCACAGCAGTTTC[A/T]GGCTTCACATTTGGG | 9100 |
| rs540976168 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84701884 | ATGCTTTTAAGTTTT[A/T]GCATGGAGAAAGTAG | 9100 |
| rs540988819 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84739473 | AGATGGGGTTTCACC[A/G]TGTTGGCCAGACTGG | 9100 |
| rs541009511 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84749326 | ACTGAGTGAAAGTCT[A/G]GTTTCATTAAAAGAT | 9100 |
| rs541012011 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84772082 | TCTGAGACAAGATCT[C/T]GCTGTGTTGCCCAGG | 9100 |
| rs541017270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84762396 | AATAACTTTTTTGTG[A/G]TAAAGGTAATGTGGC | 9100 |
| rs541046773 | snp | A/G | 4.98666e-05 | 0.00499308 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744992 | GGTGGCGATGATAGT[A/G]TCTCCACAGAAGCCC | 9100 |
| rs541047218 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84773400 | GGAACAAACCTGAAC[C/T]GAGAGTCCTCTTCTC | 9100 |
| rs541080539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84766453 | GGTCCAGGTTGGCGC[A/G]CAGCAGCGAGGGAAG | 9100 |
| rs541090167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84728496 | AAGCATGTGCCACCA[C/T]GCCCGGCTAATTTTT | 9100 |
| rs541107782 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84776705 | ATTGCTCCTCTCCTG[A/G]TCAGGGCCCCAGTGT | 9100 |
| rs541113275 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84739526 | GATTCACCCACCTCA[C/G]CCTCCCTCATTGCTG | 9100 |
| rs541113458 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84713952 | GCTGCAGCACTGGGG[G/T]TTGGCTGGGAAGGTG | 9100 |
| rs541115619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84775368 | GAGTCGGGGAGTCAC[A/G]TGAGAGTTTTACCTG | 9100 |
| rs541136879 | snp | C/T | 1.65941e-05 | 0.00288041 | intron-variant | USP10 | GRCh38.p7 | 16:84775129 | GAACCTTTCTAAAAG[C/T]GCTTCAAGCCATTGA | 9100 |
| rs541149643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84770890 | GGCCAACATGTTGAA[A/G]CCCCATCTCTACTAA | 9100 |
| rs541212598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84770703 | CGTGAACCTGGGAGG[C/T]GGAGCTTGCAGTGAG | 9100 |
| rs541231517 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84754689 | ATGGCTGATGTAGAA[A/C]CTAAAGGTTTCTGTC | 9100 |
| rs541240712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84746484 | GCAAACCTGTCCAGC[A/G]TGTTACTACTGAATA | 9100 |
| rs541254650 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84722802 | CTCAAGTGATTTGTC[C/T]GCCTCGGCCTCCCAA | 9100 |
| rs541266962 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84715648 | CTCCCTTTTTTTTTT[A/T]AAAAAACAAACAAGT | 9100 |
| rs541276395 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84774628 | GCCGCGTGCCACCAC[A/G]CCCGGGTAATTTTTT | 9100 |
| rs541277223 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84757799 | TGTGATCACAGGTGA[C/G]TTAGTCAGTCTTTGG | 9100 |
| rs541294845 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84754364 | CTCTTCTGTATTTTC[C/G]AAGTCTGAAAAGGTT | 9100 |
| rs541298320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84749761 | GGACTAAAAGAATCA[C/T]GTATAAGGGATTTTG | 9100 |
| rs541328916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84777663 | TGACTGGTGGCCTCA[A/G]TCATAAGCACTGTCC | 9100 |
| rs541332049 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84732665 | GTTGGCCAGGCTGGT[C/G]TCGAATTCCTGACCT | 9100 |
| rs541352310 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84701418 | AATAATTTTTACAAA[C/T]GTATAGCCCAAAGAT | 9100 |
| rs541354367 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84701606 | TTGTGATTTTGACAT[A/G]AAGAAAGCATCTTTA | 9100 |
| rs541359939 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84753530 | TTGCTATAGCTGAGC[A/G]TGGTGCAGCTCCTTA | 9100 |
| rs541381378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84742480 | CTGTATATTTCCCTC[C/T]CTCGCCCCCTGCCTT | 9100 |
| rs541383367 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84738323 | GTAAAAATAGAGTGA[A/T]TCAAAACACTTTTCA | 9100 |
| rs541427736 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780123 | GTTTTTGACTCTTCG[A/C]TTGGCAGAAAGGAGG | 9100 |
| rs541460001 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718573 | CCATCCTGGCCAACA[G/T]GGTAAAACCCTGTCC | 9100 |
| rs541480294 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84765329 | TCCCAAATACAGTGC[A/G]CTATGAGTAGCTCTT | 9100 |
| rs541509621 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84716848 | TCTAAACTTATCCCA[G/T]CATAATTCATCATAA | 9100 |
| rs541521697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84714441 | CTCCCTCTTTAGCCT[C/T]CCAAAATGCTGGGGC | 9100 |
| rs541532879 | snp | C/T | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698949 | AGGCTCCCTATTTTA[C/T]GTAACGTGGGAATGG | 9100 |
| rs541561032 | in-del | -/TTG | 0.02322 | 0.105218 | intron-variant | USP10 | GRCh38.p7 | 16:84744050 | ATATAGGATTCTTTG[-/TTG]TTGTTGTTGTTGTTG | 9100 |
| rs541593638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84759670 | ATGATCTGTGTTCTT[C/T]AGATTCAGTAGAAAA | 9100 |
| rs541630453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84740031 | TTTCATTGTAGCTGA[C/T]TTACATGTCCATTGG | 9100 |
| rs541657504 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84763721 | TCAAGTGGCATTGCA[A/G]TGGGTTGCAGTGGAT | 9100 |
| rs541660112 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84761051 | GGGTCTTAAGCTTTT[G/T]AAATGCTTATAATGC | 9100 |
| rs541666464 | in-del | -/TTA | | | intron-variant | USP10 | GRCh38.p7 | 16:84749923 | TTCAAGTGTGAACTG[-/TTA]TTTGAAAGGAGAAGG | 9100 |
| rs541681765 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84737755 | GTCGCCTGGCTTCCT[A/C]ATCTGTCAGAGGGCC | 9100 |
| rs541691737 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84735696 | TTCACAGAAGACGTG[A/C]CTGTGTCTCATGAAA | 9100 |
| rs541737870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84706423 | CTATATACCCCTTCT[C/T]TTGGTATTTTAAGTA | 9100 |
| rs541753125 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84712730 | ATGCATGAGTGACCC[C/G]TAAGCTGCTCTTCAG | 9100 |
| rs541780115 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84775816 | CTCCCTGCAGTATCA[A/T]TTTTTCTGCCACATC | 9100 |
| rs541787769 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84711627 | TACCTCTTTGCTCTT[C/T]TGTGCCACAACAATG | 9100 |
| rs541787799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84706898 | GGGTAGATCTGATCA[C/T]TGGAGAAGGAGAAAC | 9100 |
| rs541794543 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84716618 | TTGAGCTTTGAAGGA[C/G]AAGTAGGACTTCTTC | 9100 |
| rs541816641 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84751427 | CACTTCCTCTTCAAA[C/G]TCTGAAGTACACAGG | 9100 |
| rs541849463 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84712172 | GTATTTTGTGTGTAT[G/T]GCAGGCTTTGAGGGC | 9100 |
| rs541950336 | in-del | -/T | 0.425588 | 0.177958 | intron-variant | USP10 | GRCh38.p7 | 16:84723148 | GATCACATCCAGGGT[-/T]TTTTTTTTTTTGGCC | 9100 |
| rs541978617 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84755109 | AGCGTGTTTTTGAGT[A/C]TGTTCGAACGGGTCA | 9100 |
| rs541980194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84712936 | CAAGTGCTTGGCTGT[A/G]GGGGCTCCGTGTACT | 9100 |
| rs541989762 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84734708 | AATATCTTTAGGAAA[G/T]TCTTCCCATCCTTTA | 9100 |
| rs542011414 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84708521 | TTGCACTAGATTTAT[C/G]AGAGGACAAACTTTT | 9100 |
| rs542012903 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84735181 | GATTACAGGTGTGTG[C/T]TGCCAGGCCCGGGTG | 9100 |
| rs542072579 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84730296 | CCTACCTTTTTTACA[C/G]CGAGAGTGCTTTCTT | 9100 |
| rs542074856 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84708888 | TTTTGGTGGCCGGAC[A/G]TTAGGAGTATAGAGC | 9100 |
| rs542079912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84725198 | CACCGCCTCCCGCTC[C/T]CCCATTCTCCTCTCC | 9100 |
| rs542131805 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84767676 | AATTTGGAAAATGAA[A/T]TATGTTTTCTTCCAG | 9100 |
| rs542142608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84725561 | GCCTGCCACCATGCC[C/T]GGCTAATTTTTTTTT | 9100 |
| rs542167978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84776053 | TAACACTGCCATTTA[C/T]TGACCTTCACACATG | 9100 |
| rs542199948 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | USP10 | GRCh38.p7 | 16:84764983 | GCATTTAAAACTTGC[A/T]ACATAAAACCACCTC | 9100 |
| rs542237041 | in-del | -/AG | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84754250 | TAAGAGATTAATAAC[-/AG]AATGATACGGTATTT | 9100 |
| rs542239228 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718939 | CTGAGATTACAGGCG[C/T]CCGCCACCGCACCCA | 9100 |
| rs542242727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84705497 | CGGCCTCCCAAAGTG[C/T]TGGGATTATAGGCGT | 9100 |
| rs542279755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84734329 | GAATCTGATGTGTGT[A/G]GTAAATGGACTCTCA | 9100 |
| rs542301927 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84700724 | CCGTACTTTCACTTG[C/G]GTTTGAGTGACATCC | 9100 |
| rs542303959 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84705873 | TACAGGTGCCTGCTA[C/G]CACGCCCAGCTAATT | 9100 |
| rs542325246 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84732258 | TTGGCTTGTAAATTT[C/G]CCTGGAAGCTACTAG | 9100 |
| rs542345160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84729299 | GAAAGAAATATTTAT[C/T]GTTTTTCAAAATGTG | 9100 |
| rs542385260 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84763214 | TAGCATTTATTCCCT[A/G]CGATAACTTACACCA | 9100 |
| rs542386703 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84727717 | ATATACAGACATACA[A/G]TATTTTTCCAAACCC | 9100 |
| rs542391734 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84774722 | TGATCGCCCGTCTCA[G/T]CCTCCCAAAGTGCTG | 9100 |
| rs542422478 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84752509 | ATAATTGGAATGCGT[A/G]TTGGACTTTAGGCTA | 9100 |
| rs542427500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84777006 | TGAATAGAGACGAGG[C/T]TTCGCCCTTTTGGCC | 9100 |
| rs542465279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84722851 | GTGAGCCACTGCGTC[C/T]GGCTCAGTCGTCTTA | 9100 |
| rs542511106 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84758216 | GGAGTATTTTTACTC[A/G]CTGAACAGCCATTGA | 9100 |
| rs542526753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718618 | AAAATTAGCCCAGAC[A/G]TCGTGGCACATGCCT | 9100 |
| rs542536665 | snp | C/T | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84723506 | CTGTCAGCCCACTGA[C/T]GCCTGGGAAGTCACA | 9100 |
| rs542546821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84756418 | GCCAACATGGTGAAA[C/T]CCTGTCTCTCCTAAA | 9100 |
| rs542555602 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84747514 | TGATAGGCCAGACGT[C/T]GTTATTTTGGGCTTC | 9100 |
| rs542574212 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84709744 | GTCTCTTGTAGAACG[C/G]TGACATTTGAGCTGG | 9100 |
| rs542636485 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84774661 | ATTTTTAATAGAGAC[A/G]TGGTTTCACTGTATT | 9100 |
| rs542647419 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84736865 | GTGATCTCGGCTCAC[A/T]GCAAGCTCCGCCTCC | 9100 |
| rs542652071 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84709309 | CATGAGACAGTGGGG[A/G]CAGCATGTGTGGTGG | 9100 |
| rs542652977 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84726233 | GTGCCGTGCTGTACT[A/G]ATAGTCCCCAGCGTC | 9100 |
| rs542689263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84749253 | AGATCCACTACCACA[A/G]ATTCCCTTTAGTGGG | 9100 |
| rs542710784 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84737272 | TGTGCGTTTAGCATA[A/C]CTATTAATAGATGAC | 9100 |
| rs542753924 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84749062 | CAGAACGTAGTTGTT[A/G]ACAGTTTCAGGAGTC | 9100 |
| rs542797390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84727684 | TACAGACACACAGAC[A/G]TGGGCTAACAAATGC | 9100 |
| rs542840149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84776633 | CGCCTTCTCCCTGCA[C/T]CTCTTCCCCTGGAGG | 9100 |
| rs542849595 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84745866 | GAGGAGAGGGTTGTC[A/G]TAACTTTATGTTAAG | 9100 |
| rs542866691 | snp | A/C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84740946 | GTATTGCTTAAGTAC[A/C/G]CAGCGTTGGAATACC | 9100 |
| rs542870336 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84765972 | CGAAAGTACTGAAGA[G/T]GCCTCATTGGAGCCT | 9100 |
| rs542902006 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84713509 | CTCTCGTCCTCCCCC[A/T]ATGTAAGCTCCTTGA | 9100 |
| rs542940457 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84760863 | TTCTTTCCTCCCAGA[A/C/T]TGAGTTTGTGATGAA | 9100 |
| rs542949999 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84720705 | TCCTGCCTCAGCCTC[C/T]TGAGTAGTTAGGACT | 9100 |
| rs542950585 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84756226 | GCATTCATCTCTGTG[C/T]CTTCCTTACCCGGTG | 9100 |
| rs543003924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84731330 | GCAGGGCTACGCCAT[A/G]GGCAATGTGCACAGA | 9100 |
| rs543026368 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84700009 | CGATGCGAGTGTGTA[C/T]GTGCGGGCGAGAAGA | 9100 |
| rs543030747 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84770079 | ACGCCACTGCACTCC[A/C]GCCTGTGCGATAGTG | 9100 |
| rs543053902 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84749808 | ACTCTTGATTACTCT[A/T]AAACTATCCACTTTA | 9100 |
| rs543059144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84740172 | ACTGACTCTTCATGT[A/G]TGTTATTCTGCTAGA | 9100 |
| rs543069098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84726605 | GCTTGCCCCCCTTTT[C/T]TCGAAGTGTTTCTTG | 9100 |
| rs543072812 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84736914 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 9100 |
| rs543104923 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84721307 | GGTGTACTGAAGAAT[A/T]CTTCTTCCGTAGATG | 9100 |
| rs543162201 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84723669 | AGTCTACTGCATTAA[C/T]TTCTGGCTAAACAAA | 9100 |
| rs543165567 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84721813 | AGCAATTCTCCTGCC[C/T]CAGCCTCTCGAGTAG | 9100 |
| rs543205370 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84761831 | CAAGGGGCAACCTTG[C/G]AAGCAGGCCTTTCCA | 9100 |
| rs543230801 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717765 | GTGTTCAGGAAAGTG[C/G]TTCTACTGCCTTTGA | 9100 |
| rs543329517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84742803 | AGATGATCAAACATG[A/G]TATTGAGTAAATGTT | 9100 |
| rs543364202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84712015 | ATGAGCCACCGCGCC[C/T]GGTGGCTTTTGCTTT | 9100 |
| rs543397508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718964 | CACCCAGCTAATTTT[C/T]GTATTTTAGTAGAGA | 9100 |
| rs543402674 | snp | C/T | 0.00018235 | 0.00954682 | intron-variant | USP10 | GRCh38.p7 | 16:84758825 | ATCCTTCCTGGACGC[C/T]GTCCGCAAGGCCAGC | 9100 |
| rs543403555 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84768417 | GGTTTGGTGGAAAGA[A/C]CACAAAATTAGGAAT | 9100 |
| rs543427670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84714588 | TCTTCAGCATTGTTT[C/T]TTAAGGACTGCAGCG | 9100 |
| rs543464873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84767799 | TAATTTATTTTTTTA[C/T]TGATAATTCTTGGGT | 9100 |
| rs543465778 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84762911 | GGAGGCATGGTTGGA[A/C]TTTGCAAGTACTGCA | 9100 |
| rs543473074 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | USP10 | GRCh38.p7 | 16:84774634 | TGCCACCACGCCCGG[C/G]TAATTTTTTGTATTT | 9100 |
| rs543483741 | in-del | -/A/AGAGAAAA | 0.167158 | 0.235875 | intron-variant | USP10 | GRCh38.p7 | 16:84764931 | CCACGAGAGAGAGAG[-/A/AGAGAAAA]AAAAAAAAATATATA | 9100 |
| rs543490882 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84737039 | GTGGTCTGCCCGCCT[C/T]GGCTTCCCAAAGTGC | 9100 |
| rs543570322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84775677 | TGAGAGGGTGGGCCC[A/G]ATTACACAAGCTCCT | 9100 |
| rs543577499 | snp | C/G | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698349 | ATCTCCTCACAATAA[C/G]GACATTCTCTCAGTG | 9100 |
| rs543594388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741980 | TTTATTCTGCTCCCT[C/T]CCACTACCTCCAGCT | 9100 |
| rs543615944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84733205 | TTGTTTCAAAATAAG[C/T]TTTATCAGTTTCATA | 9100 |
| rs543617826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751076 | ACAGACCGCATGTAC[A/G]ACAGTGGTCCCATAA | 9100 |
| rs543623413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84771468 | CCACTGCACTCCAGC[A/G]TGGGCAACCAGAGTG | 9100 |
| rs543624854 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84761533 | ACTCCTCTCCCAGTG[A/G]GGCCACAAGGCTACG | 9100 |
| rs543650822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84711660 | TTCTAAGTTAGGTGC[C/T]AGCAGCAGAAACTTT | 9100 |
| rs543700030 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84720231 | AGAGGAAGCTCTGCC[A/G]TGGCGATGTGCGTTC | 9100 |
| rs543709254 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84747797 | GCCTCAAACTCCTGA[C/T]CTCAAGTGATCTGCT | 9100 |
| rs543779121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84739166 | CGGGTTCACGCCATT[C/T]TCCTGCCTCAGCCTC | 9100 |
| rs543783547 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717253 | ACATGCATTCTTTAG[A/G]GGGTGGGCCTAATTC | 9100 |
| rs543783881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84776580 | CTGGCTCCTTGGAGT[A/G]TGGCACCCAGGTCCC | 9100 |
| rs543786994 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84750087 | GAGAGGAGATGGTTG[C/G]CATTTATCAGTAGGA | 9100 |
| rs543797917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84759204 | AGGACACTTACCCTA[A/G]TAACTATTTGGTTTA | 9100 |
| rs543861200 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84732580 | GCCTCCCGAGCAGCC[A/G]GGACTACAGGTACAC | 9100 |
| rs543866337 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84712534 | TGTCATTCACTGTTT[C/T]CAGGACTGCTTATGG | 9100 |
| rs543886546 | in-del | -/GA | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84751514 | CCACCCTTGTGGACT[-/GA]GAGTTTAGTCCACAT | 9100 |
| rs543915394 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84772114 | TGGGGTACAGTGGCG[C/T]GAACTTAGCTCACTG | 9100 |
| rs543943323 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84747058 | CGGCAGGACGTTTCA[C/G]TTCCACTAGAATCTT | 9100 |
| rs543968962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84714989 | GGCTGGAGTGCAGTT[C/T]GCAGTCTCGGCTCAC | 9100 |
| rs543982497 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84708928 | AATTCCTGTGCTTTA[C/G]AGGTTCGCTGGGTAG | 9100 |
| rs543997184 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84706515 | GTATTTATATTTATT[A/T]ATATTTTTATATTTA | 9100 |
| rs544002371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84736211 | GTGGCATGAGTTACA[A/G]TCTAGTCGAATTTTT | 9100 |
| rs544004343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84731037 | CAGGCTGGAGTGCAG[C/T]GGCTCATTCTCGGCT | 9100 |
| rs544011142 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84755974 | AGCACTGCTGCCCCA[G/T]TCAGTGAGAACCTTC | 9100 |
| rs544045572 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84767365 | GAAATGAAAAACCAG[C/T]TAAGAAAACAAGGTC | 9100 |
| rs544054649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84706803 | CCTCGGCCTCCCAGA[A/G]TGCTGGGATTACAGG | 9100 |
| rs544056743 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | USP10 | GRCh38.p7 | 16:84701977 | AATTTGGCTCTTGTT[G/T]CCCAGGCTGGAGTGC | 9100 |
| rs544065583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84731479 | ATTCTTGTATTTCTC[A/G]AATTCATTTTCTGGA | 9100 |
| rs544089653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84729906 | GGTGTATTTTTTTGC[A/G]TGACATGTTTTCATC | 9100 |
| rs544127798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84763769 | GTTGTGATTGGTTGC[C/T]GTGGATCCAGTGACG | 9100 |
| rs544135459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84778725 | TTATGGATTGCTTGC[A/G]TGTTTGAGTTGAAAT | 9100 |
| rs544135915 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84728392 | TTGCCCAGGCTGGAG[A/T]TCAGTGGTGCGATCT | 9100 |
| rs544174945 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84773177 | GGCACTTTTTGAAAG[C/G]AATTTTAAAGAGCCC | 9100 |
| rs544209473 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84726696 | GTTTTGAAAGCCCGG[A/G]ATGGAGGCCGGATGG | 9100 |
| rs544238562 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84752151 | CTACAGGTTTCAATT[A/T]TGTGTCTTTTATGAG | 9100 |
| rs544254723 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84708049 | TGCCACTGCACTTCA[C/G]CTTGGGTGACAGAGC | 9100 |
| rs544298596 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84751784 | GTCGATTACGGGCCA[A/G]TTATTGAGCCCTAAG | 9100 |
| rs544334578 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84740397 | TCTCCTTATTTCCCT[C/G]AAGGGAATTTGGCCA | 9100 |
| rs544352420 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699080 | TAACAATCCCAGTAG[C/G]CAATTTTTATTGACT | 9100 |
| rs544392799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84704679 | TTTATCATAAACCTC[A/G]ATGTAGAATCTTCAG | 9100 |
| rs544418106 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84778578 | GCCAGGTCTGTAGGC[A/C]TGTACAGCTGATGGC | 9100 |
| rs544431749 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84705017 | TGGTGGCTGCTCCTA[A/C]GAGTCCTCAGTCTCC | 9100 |
| rs544454977 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84720878 | TGGGCCACCGCGCCC[A/G]GCCAATGATGCACAA | 9100 |
| rs544460308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84759695 | AGAAAATATTTTAGC[A/G]TTTACCAGCATATAT | 9100 |
| rs544467733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84725584 | TTTTTTTTGTGTTTT[C/T]AGTAGAGACAGGGTT | 9100 |
| rs544492966 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84710599 | AACAAGCATCTGTCC[C/G]TTGATTATATTCGTA | 9100 |
| rs544515816 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84700052 | GGGAAGCAGCGTGAG[A/C]AGCCGGAGGATCGCG | 9100 |
| rs544535191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84769363 | CCAGGCTCTGGGGGG[A/G]TCAGTAGAAGTTATG | 9100 |
| rs544598137 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84765993 | ATTGGAGCCTAATTT[A/C]CTTTCTGAGGCCTTG | 9100 |
| rs544652587 | snp | G/T | | | synonymous-codon, intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84740335 | CAGTGGAACAGTTCT[G/T]TGTGGCACACAGGCT | 9100 |
| rs544655398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84765519 | TGTATAAGTGAGACC[A/G]TGCAATATTTTTCTT | 9100 |
| rs544661460 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84708026 | GACATTGTAGTGAGT[C/T]GAGATTGTGCCACTG | 9100 |
| rs544681740 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84760946 | TAGTTGAGAAAATGC[C/G]ATTTAAGTCAAGTTT | 9100 |
| rs544704348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84701815 | AGTAGCAAAAGTTGG[C/T]GGAACGTAAATGTTA | 9100 |
| rs544744619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84760415 | AGAGTCCATTGCTTG[A/G]ATGATATGGTGCACC | 9100 |
| rs544747037 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84764815 | AGCATGGGTGACAGA[C/G]TGAGACTCTGTCTCA | 9100 |
| rs544790014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84770347 | AAGTTTTTAAAATGC[C/T]ACCTTTAACTTTATT | 9100 |
| rs544792960 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84706881 | CCTGAAGTAGGCTTT[C/G]TGGGTAGATCTGATC | 9100 |
| rs544801648 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84722498 | CAAAGCGGCCATGCC[A/G]TTTTCTATCTGCACC | 9100 |
| rs544967542 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84713989 | TGCGTCTTGTAGGCT[A/C]TGCTAGAGCCTTTTA | 9100 |
| rs544978106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84775077 | AGTTTACTTGCTGGG[A/G]AGAATGTTGTTAGCC | 9100 |
| rs545004296 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84734089 | CACTCAATGTATTTT[A/G]TCATGTCTCCTGGTG | 9100 |
| rs545035008 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84739666 | GAAGAAGAAAAATTT[A/T]AGTTATTTTTGAGAT | 9100 |
| rs545048746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84778596 | TACAGCTGATGGCTG[C/T]GTAGGAGTGTCTGTG | 9100 |
| rs545089822 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84733012 | CCTTTTTTGGATTTC[C/G]TTGTCTTCCCATTTG | 9100 |
| rs545105169 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84774618 | TGAGACTACAGCCGC[C/G]TGCCACCACGCCCGG | 9100 |
| rs545148341 | snp | A/G | 6.67991e-05 | 0.00577885 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744916 | CTCAGGTGGTCTTGG[A/G]CAAAGGGAGCGTAAA | 9100 |
| rs545151024 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84740797 | CTTGCAGTTCACATT[C/T]ATGTCCTGGTCTGTC | 9100 |
| rs545209976 | snp | C/G/T | 0.000259069 | 0.0113789 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745257 | GCTTCCCTGCAGAGG[C/G/T]TGGCAGAGACACCCT | 9100 |
| rs545264629 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84752898 | TAAGAGAAAATCTTT[G/T]ACAATAAGTATTTAA | 9100 |
| rs545274301 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84753710 | AGCTAAATGACCTTT[A/C]AAGTCTGTTGAGTCA | 9100 |
| rs545284313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84740901 | TAAGCTGATTGCCAG[A/G]GATGGTGCTTATGGA | 9100 |
| rs545285635 | in-del | -/GGT | | | intron-variant | USP10 | GRCh38.p7 | 16:84737492 | GTTTGCTGAATGAAA[-/GGT]GGTGCTGTGTGCCTG | 9100 |
| rs545285971 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84753258 | AAGTGTTGCCTGAAA[C/T]AGAACTTTATTAATA | 9100 |
| rs545320537 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84761866 | GAGCCACCCAGGCCT[G/T]CTATGAAAAGTCTTC | 9100 |
| rs545320878 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84736802 | TTTGGTGTGTTTTCT[G/T]TTTTGAGAGGGAGTC | 9100 |
| rs545326225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84757098 | AATTATGAATAATAT[A/G]CACAAAGCTTCTAGC | 9100 |
| rs545340429 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84757724 | TTAAAAGTAAAGGAG[A/G]CAGTGTGGATTGGCT | 9100 |
| rs545350338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84736979 | GGTTTTAGTAGAGGC[A/G]GGGTTTCACCGGGTT | 9100 |
| rs545350707 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84702090 | AGACGGGAGTCTTGC[A/T]CTGTCGCCCAGGCTG | 9100 |
| rs545409514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84776741 | CACACACCCCTCCCC[A/G]ACTCTGCAACCTGCC | 9100 |
| rs545432320 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP10 | GRCh38.p7 | 16:84750579 | CGTTTGAAATTGAAC[A/G]TATGCTTTCATTGAA | 9100 |
| rs545444474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84775320 | CTTAGCATAGCGACC[A/G]GATGCTGTACTCAGG | 9100 |
| rs545472255 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84725085 | TAAATATGCATTTCA[G/T]TGGTTTTTAGTGTAT | 9100 |
| rs545472381 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717838 | TCAGTACGGATTAAT[G/T]TACTGTAATGCTTAA | 9100 |
| rs545504149 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84754398 | TCTGCGTTTAACGAC[A/G]TCGTACCAGAATGGC | 9100 |
| rs545524336 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84754334 | ATCATTAAGAAAAAT[C/G]TAGGTTGTTCGTGTC | 9100 |
| rs545536677 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84720416 | TTTGGCAGTAATTGT[C/G]TTTGTGTGGAGTTTG | 9100 |
| rs545541338 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84742971 | TGAATGACACAACAC[C/G]TTCTAGTTTCTAATG | 9100 |
| rs545583577 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84758269 | TCAGCATTAGATGCT[A/G]GGGATGCAGAGAGGA | 9100 |
| rs545667880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84767597 | GCAGCGTTTTGAGGC[C/T]ATGGCAGGGTGGCTG | 9100 |
| rs545693751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84710141 | CGGGCGTGGTGGCGC[A/G]TGTCTGTAATCCCAG | 9100 |
| rs545724256 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84737353 | GCTTTGATTTTTGAA[C/G]TTTGTATTCTTACAA | 9100 |
| rs545769649 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84756446 | AAAAATACAAAAATT[A/C]GCCGGGCGTGGTGGT | 9100 |
| rs545772404 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84715645 | GCCCTCCCTTTTTTT[A/T]TTAAAAAAACAAACA | 9100 |
| rs545775723 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84720039 | CTCATTAAGGTGGAA[C/G]TTCTGTGCTTGATCT | 9100 |
| rs545838511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84711351 | ACCTTTGTGGACAGC[A/G]TGGGATCAGCACACT | 9100 |
| rs545845199 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84769762 | CTGCCTAGGGAAGAC[C/G]CTTTTGTGATGTGTC | 9100 |
| rs545882856 | snp | A/T | 0.000458004 | 0.0151259 | intron-variant | USP10 | GRCh38.p7 | 16:84759332 | GTGTGTCTGTTCATT[A/T]CCTTTACGCTTCCTT | 9100 |
| rs545928508 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84733626 | ATGGAGACTAATATG[A/C]GAAATGCCTCAACCC | 9100 |
| rs545929525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84768802 | TGTAAATATAATATA[A/G]TCATTGTAAATATAA | 9100 |
| rs545933781 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84716538 | ATGAGAATTACTATG[A/C]AATATGAACAGTGCT | 9100 |
| rs545944238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84758958 | TGCCTACCTTGCTTA[C/T]AAACAGGATTATTCC | 9100 |
| rs545948438 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84716180 | GTAATGTCTCTCCCC[C/G]CTCTCCTTTTCCAGA | 9100 |
| rs545983951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84728790 | ATTCTGTTTTATAAG[C/T]AGCACCTCTTCTTTT | 9100 |
| rs546003283 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84712051 | GTGGACAGAAACACC[G/T]TGCAGCTGTGCTTCG | 9100 |
| rs546009430 | snp | C/T | 4.97137e-05 | 0.00498542 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84763033 | AGGCTTCATTCTAAA[C/T]GGACTTCATGAGGAA | 9100 |
| rs546022448 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84708101 | AAAAGATAAGAAATA[G/T]TTTGAAGACTTCCAC | 9100 |
| rs546051824 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84707371 | CATTTTAATAAAGTC[A/G]TTTATTTTATTTTCT | 9100 |
| rs546065914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84747118 | TGACCGAAATGTTAC[A/G]CCGCGCGTGACTGTA | 9100 |
| rs546093838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84771512 | AAAAAACAAACAAAC[A/G]AAAAAACCCACCTAA | 9100 |
| rs546104926 | in-del | -/GGTTAAAC | 0.00358779 | 0.0422022 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719872 | AGATCATTAGGTGAA[-/GGTTAAAC]TGAGACAGCAAACAG | 9100 |
| rs546113743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84703150 | GAAACATTTTGAGAC[C/T]GGTAACTCAGCATTT | 9100 |
| rs546191620 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779675 | TCAAATATTTGGAGT[G/T]AAAATGTTAGTCTAC | 9100 |
| rs546191837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741983 | ATTCTGCTCCCTCCC[A/G]CTACCTCCAGCTGCA | 9100 |
| rs546263361 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84725853 | CATGCCAAACAGTCT[A/G]TTGCTCTTTTCATGT | 9100 |
| rs546264409 | snp | C/T | 1.65861e-05 | 0.00287972 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764208 | AAGACTTCCGTCACC[C/T]GCCAGGCGGATTTTG | 9100 |
| rs546287619 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84706832 | GGCGTGAGCCACCGC[A/G/T]CCGGGCCAAGACTAT | 9100 |
| rs546302205 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84773184 | TTTGAAAGCAATTTT[A/T]AAGAGCCCCAGGTTA | 9100 |
| rs546307446 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699357 | TTGCCCGTGCACACG[C/G]ACGCACGTGTGCAAC | 9100 |
| rs546331714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84773119 | GGCGCACAAATAAGA[C/T]GTGGCACTTACCAGC | 9100 |
| rs546363722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84776155 | GTTTTATAAAAGAAT[A/G]AACCAGAACTCAAGG | 9100 |
| rs546440974 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84746831 | TATTTTACTTTTAAA[-/T]TAAAAATTCTAAACT | 9100 |
| rs546465096 | in-del | -/GTGGGGGTGTGT | 0.28052 | 0.24813 | intron-variant | USP10 | GRCh38.p7 | 16:84757397 | GAGGGAATGAGAGGG[-/GTGGGGGTGTGT]GTGTGTGTGTGTGTG | 9100 |
| rs546476967 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84721442 | CTGCTTTACATAGAT[A/T]GTGCATAACAATTTT | 9100 |
| rs546480703 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84763408 | TGCTATACACACACT[A/G]TGTATATATATATAT | 9100 |
| rs546493515 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84741189 | AGAAGCCTTGAAAAG[A/C]CTAACCAAACGTTTT | 9100 |
| rs546516309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751141 | GTGAGTTGTGTTACA[A/G]TTGCCTACGGTATTC | 9100 |
| rs546519738 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84775432 | CCCTGAGGACAGATA[A/G]CAGAAGACCTTGCTC | 9100 |
| rs546546657 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84751593 | CAGAAACATAAGTTG[A/T]TCTGTAGTCAATGGG | 9100 |
| rs546574469 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84773985 | CTGGGCGCAGTGGCT[C/T]ACACCTGTAATCCCA | 9100 |
| rs546576073 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84752505 | CTCCATAATTGGAAT[A/G]CGTATTGGACTTTAG | 9100 |
| rs546597010 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84751937 | TGACATAAAAGTTTA[C/T]GATGCTGGTATTGCC | 9100 |
| rs546686272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84768668 | TACCTCTGACAGAGG[C/T]CAAATAGCTTATTTA | 9100 |
| rs546735129 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84720712 | TCAGCCTCCTGAGTA[C/G]TTAGGACTACAGGTG | 9100 |
| rs546746913 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84748729 | TGTTTTAGAACATTC[A/T]ACTTAGTCATATGAC | 9100 |
| rs546760130 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84748307 | TGAGAATTTTATTTT[A/C]TTTTCTTTATTTTTG | 9100 |
| rs546799570 | in-del | -/T | 0.00107145 | 0.0231209 | intron-variant | USP10 | GRCh38.p7 | 16:84762982 | TGATTATATTTGACC[-/T]TTTCAGGGTCGACAA | 9100 |
| rs546810464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84752415 | ATGACTTTGGAATGC[A/G]GGTCAAGTTTCAACC | 9100 |
| rs546938114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84713346 | AGTGAGTCTCTGTGC[C/T]TGGGCCATCTTCTTA | 9100 |
| rs546969096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84720235 | GAAGCTCTGCCGTGG[C/T]GATGTGCGTTCCTTC | 9100 |
| rs546989296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84774007 | GTAATCCCAGCACTT[C/T]GGGAGGCCGAGGCAG | 9100 |
| rs546990519 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84721474 | AAAAAGTCAACCTTA[C/T]TGAAGTATAATTTAA | 9100 |
| rs547012073 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84725361 | CCTGTTGTAGCATGC[A/G]TTAGTCTGATGACAT | 9100 |
| rs547022786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84735315 | ACGTTTTAGTTGCTA[C/T]AGGTTTTCTCAAGTG | 9100 |
| rs547036978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84777526 | GGATGAAGCTATGCC[C/T]TTGGATTGGCTGTGT | 9100 |
| rs547050781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84773762 | TCCCCATTTTATTCT[A/G]TCCATCGGGAAACCT | 9100 |
| rs547081234 | in-del | -/AGT | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84701894 | TTTTAGCATGGAGAA[-/AGT]AGTAGCAAAGGAAAT | 9100 |
| rs547112015 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84776779 | GGGACCTGGGCCTGG[G/T]TTGCTCTCCCCTGCC | 9100 |
| rs547167292 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84710471 | GGACTTTTGAGACAG[A/G]TTAATGTGAGGCAGG | 9100 |
| rs547173104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84743082 | ACGGCCCCAGAACAT[C/T]AGGGAATAGGGGATG | 9100 |
| rs547190980 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84739465 | TTTAGTAGAGATGGG[G/T]TTTCACCATGTTGGC | 9100 |
| rs547229051 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84706182 | GCCACCGCGCCTAGC[C/G]TCCCTATTCATTCTG | 9100 |
| rs547229080 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84710951 | GTATTTTGGACAAAG[A/T]GTTACATCTCCAGTC | 9100 |
| rs547231755 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84746107 | TGGTTTTTTTTTTTT[G/T]GATTGAGTAAATGGA | 9100 |
| rs547260487 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84715147 | ATTGGCCGGTCTGGT[C/G]TCGACCTCCTGACCT | 9100 |
| rs547273433 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84756227 | CATTCATCTCTGTGC[C/G]TTCCTTACCCGGTGC | 9100 |
| rs547291399 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84706610 | CAGTGGCGCAATCTC[G/T]GCTCACTGCAAGCTC | 9100 |
| rs547294351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84764578 | GTTCATGCCTGTAAT[C/T]CCAGGACTTTGGGAG | 9100 |
| rs547328605 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84735445 | CTGAAGGCCTGGGGT[A/C]GCTTCAGTTCTGCCA | 9100 |
| rs547337688 | snp | A/C | 2.80895e-05 | 0.00374753 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84760260 | GACAGTTAACAAGTC[A/C]AGCCTGTCTGAAAAG | 9100 |
| rs547344138 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84744595 | TACTTAGAGTTTGTA[C/G]AACTGGGTTCTTAAC | 9100 |
| rs547356048 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84734754 | TGTCTGTTTTCTTCT[A/G]AAAGTTTTCAGATTT | 9100 |
| rs547407515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84740579 | CGGAGTGCCAGCCAT[A/G]TAAGATTTAGTTTAG | 9100 |
| rs547428836 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718731 | ACTGCACTCCAGGTT[A/G]GGCAACAGAGCAAGA | 9100 |
| rs547466686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741017 | CAATTCAAACTTGTC[A/G]AGATCATTTTTCAAT | 9100 |
| rs547493366 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84714844 | AAACATGAATTTTTT[A/T]AAATTTTAAAAGTAA | 9100 |
| rs547497834 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719250 | ATTATTTTATAATTT[C/G]TTTTTTAACTGGGAG | 9100 |
| rs547556364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84736622 | AAGAAAGAGAAAATG[C/T]TCACCATTCTTTAGT | 9100 |
| rs547571100 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741393 | GGCTGATGTCAACCT[C/G/T]TCAGACATCTGAGTC | 9100 |
| rs547620987 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84731817 | AATTTTTTCTGCTTC[C/G]TTTTAGCCTATAGAA | 9100 |
| rs547630530 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741720 | CCACCAGTTTGCACA[C/G]TTAGTGACAGGCCTG | 9100 |
| rs547642905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84700514 | AGGGGCCCCAGAGCA[A/G]CTCAGGTTGCTGCCT | 9100 |
| rs547662445 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84770435 | GGATTATATGAAATA[C/T]TTGCTATATAGAAAA | 9100 |
| rs547673403 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84750359 | GTTCAGTGAGCCCAG[A/T]TCGTGCCACTGCACT | 9100 |
| rs547710374 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84733335 | TCTTGGGGGTTATGG[C/G]CCAAATGTTGCATAG | 9100 |
| rs547715839 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84753799 | TTTAATTGATCCTGT[A/G]TTACTGTCTAATGAG | 9100 |
| rs547760354 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84770468 | TCTGCCTTTGTTGAG[G/T]GATTAGAAATTAAGC | 9100 |
| rs547788026 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84746466 | GCCTATTACTCCCGG[A/G]CTGCAAACCTGTCCA | 9100 |
| rs547792983 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745205 | AGGACTGCAGGGCAG[C/T]CAGAGGGGGGCCCCG | 9100 |
| rs547798576 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84738968 | AGTGAACAGACTTTG[G/T]GAAGTGCTGCACCAG | 9100 |
| rs547807428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84749643 | TTTATCTCAAGTTTG[C/T]TTCAAATACTCACAT | 9100 |
| rs547815228 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84766640 | GGGTCAGCATACTCA[A/C]AGATCCCAAATTTGT | 9100 |
| rs547859663 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719375 | TTGGATCACGGGAAT[A/G]CCCCTACACAGTGAT | 9100 |
| rs547885757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84747127 | TGTTACGCCGCGCGT[A/G]ACTGTACGTACCTAA | 9100 |
| rs547908707 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84775510 | CCAGGCTGGCTGTTT[A/C/G]AGAATGTGACCTCTC | 9100 |
| rs547915806 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84709916 | GTCTGGAGAGGAGAG[A/G]GAAAGAATTTGGTAA | 9100 |
| rs547926307 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84763817 | GGTTGCCGTGGATCC[A/G]GTGACGTTGTGCCTG | 9100 |
| rs547970978 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779223 | AATGAAAAGGAGATG[A/C]CTTGGGGTTCGTGCA | 9100 |
| rs548003412 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84710862 | CAGGTTGCAGGTCGT[A/C]CGCATGGGTTTGTGT | 9100 |
| rs548020878 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84734841 | GTGTGAGGTGGCATC[A/G]AACTCCCTGCCCCTG | 9100 |
| rs548023645 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84770100 | TGCGATAGTGAAACC[G/T]TGTCTCTAAAACATA | 9100 |
| rs548065322 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84777861 | GCCACTGATGGTGGG[C/T]GCAGCTTAGCAGGCT | 9100 |
| rs548100320 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84732883 | TCAGGCTTGCAACAA[A/G]GGCTGTGTCTGTCTG | 9100 |
| rs548143234 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84722684 | CTCCTGCTAGCCTCC[C/T]GAGTAGCTGGGATTA | 9100 |
| rs548145037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84727763 | AAGATTACATACACT[A/G]TAGCCACTTAATCCT | 9100 |
| rs548174334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751616 | TCAATGGGTAGTGGT[A/G]CATTTTGGTCACTTT | 9100 |
| rs548177344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84772191 | CAGGTAGCTGGGGTT[A/G]CAGGCGCCCACCACC | 9100 |
| rs548212096 | snp | A/G | 1.66685e-05 | 0.00288686 | intron-variant | USP10 | GRCh38.p7 | 16:84763103 | AGTAGGTTATGGTCC[A/G]CTTGCCGCAGAGTTG | 9100 |
| rs548235426 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84709779 | TTTCAGGCAGAGAAG[C/T]ACACGGACAAGGGCA | 9100 |
| rs548258401 | snp | A/C | 0.000798403 | 0.0199641 | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780312 | GGAAGCCTTCTGAGA[A/C]GGAAGACATGGAGAG | 9100 |
| rs548261120 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84775291 | GTTTACAGCTGGGCA[A/C]AGGTTTGCTGCAACT | 9100 |
| rs548270627 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84743208 | TAGCCAAAGGAATTA[A/G]ATGGTCGTGACTTCA | 9100 |
| rs548281139 | in-del | -/T | 0.00835141 | 0.0640778 | intron-variant | USP10 | GRCh38.p7 | 16:84748929 | CTACCAAACAGATTA[-/T]TTTTTTAATCCTATT | 9100 |
| rs548308266 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84708126 | TTCCACCCCCTTAGT[A/C]GTAGTCATGCTGTCC | 9100 |
| rs548320909 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84778830 | TGGAGGGAAGTCGGC[A/G]GAGACCTGTAATGAT | 9100 |
| rs548365408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84728925 | TGCATCAGCCTCCCA[A/G]GTAGCTGGGATTACA | 9100 |
| rs548367085 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84703685 | AAGCTATTTAAACAT[A/G]TCCTAAGAGTAGATG | 9100 |
| rs548374262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719648 | AGAATATAGGAAGCC[A/G]ATTGGGTGGAAAACA | 9100 |
| rs548435899 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84720056 | TCTGTGCTTGATCTT[A/T]ACACCGGAAGGAGAG | 9100 |
| rs548460992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84758981 | ATTATTCCTGACCCC[A/G]GTCCATCTCCCTCTA | 9100 |
| rs548465163 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84754578 | GGTGGTGCTAGAAGA[C/G]TTGATTTTAATACTG | 9100 |
| rs548465759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84742276 | GCAATTCAGTGATCC[A/G]TCAAGTTCCACTGAC | 9100 |
| rs548477603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84763828 | ATCCAGTGACGTTGT[A/G]CCTGTTGGGATTGGT | 9100 |
| rs548527300 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84702198 | AGTAGCTGGGATTAC[A/G]GGCGCCCACCACCAT | 9100 |
| rs548530464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84720772 | ATTTTTTAATAGAGA[C/T]GGGGTTTCACCGTAT | 9100 |
| rs548531026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84775893 | TATAGCGTCATCTTT[C/T]ATGCCTCTGAGTCTT | 9100 |
| rs548532128 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84705087 | TTCTTCGGATCCATT[C/G]TCAGTTTATTTTTCT | 9100 |
| rs548555529 | in-del | -/G | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84728017 | TTTTGTAGTCTGGAA[-/G]TTTCCCACAGCCTTT | 9100 |
| rs548565851 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84728373 | CTTTTTTTTTTTCTC[A/G]CTGTTGCCCAGGCTG | 9100 |
| rs548596588 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779982 | TGAAATTCATGGGGG[A/C]ATGAGTTTGCCTGCA | 9100 |
| rs548621349 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84728618 | ACAGGCGTGAGCCAC[C/T]GTGTCCGGCCTCCTT | 9100 |
| rs548624991 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84716115 | TGGGTGACTACTATC[C/G]CACAGGGTAGGAAGG | 9100 |
| rs548630634 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84721550 | TCTTTGTTTTTCAGA[C/T]GAGGTCTTGCTCTGT | 9100 |
| rs548669659 | in-del | -/CT | | | intron-variant | USP10 | GRCh38.p7 | 16:84727208 | CTGTATTTTATCTTG[-/CT]CTGTTATGGGCAAAA | 9100 |
| rs548677374 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84769516 | CTGGCGGTGGACCTC[A/G]TGGAAGAGAGAGAGG | 9100 |
| rs548686703 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84760582 | GCTTTCAAGTCAGTT[C/G]TCTTAACCACTGCAC | 9100 |
| rs548738365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84769087 | TGGCAGTGAATTCAT[A/G]AAAATGCACTGGGGA | 9100 |
| rs548749259 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84764649 | CAACCTGATCAACAT[A/G]GTGAAACCCCGTCTC | 9100 |
| rs548756861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84722446 | GTAAAATGTGGTAAG[C/T]GTATATTCTATTCTG | 9100 |
| rs548809757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84763536 | CTAAAGCATCTCCTG[C/T]GTAACCACAGTCCCT | 9100 |
| rs548815101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718295 | ATTGTACTCTGTGAC[C/T]CAAGATAGAGTGCAG | 9100 |
| rs548826170 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84715779 | TTCAGCCGTTTAGTT[A/C]CAGTTTTGAGGACGT | 9100 |
| rs548827650 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84771332 | TGAGGCGAGCAGGTT[A/G]CTTAAGTCTAGGAGT | 9100 |
| rs548855895 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84740604 | GTTTAGGAAATGGTT[G/T]TTGAGTTCTTTTTTT | 9100 |
| rs548871845 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84700722 | GACCGTACTTTCACT[G/T]GCGTTTGAGTGACAT | 9100 |
| rs548908752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84768030 | CAAAGCACATCTTCA[A/G]CAGAATTATTTTTAA | 9100 |
| rs548915077 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84778305 | TCTTTAGGATAGATG[C/G]GCCACAGAAGGCCTA | 9100 |
| rs548957626 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84713675 | GACATATTCAGAAGC[C/G]CACAGTCAGGTGTGG | 9100 |
| rs548978183 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84748418 | AGGCAATTCTCCTGC[C/T]TCAGCCTCCCTAGTA | 9100 |
| rs548989990 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84700312 | CTGAGCCACCCGGAC[C/G]CCCTAGTCCCGGGGA | 9100 |
| rs549012779 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84776240 | CCACCTCAGCTCACG[C/G]CCGATGTTTTAGGAA | 9100 |
| rs549131612 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84707263 | ACATTTACAGAATGA[A/G]TGAATGAAATGTGCA | 9100 |
| rs549159479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84717054 | GTTGAGAATCAGCTG[C/T]GGGTCTTGTGAATGT | 9100 |
| rs549203959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84704455 | TGTCATTTGTCACTT[C/T]AGTGCCACTTCAGCA | 9100 |
| rs549222642 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84712770 | TGCTCTCTTTACCTC[C/T]GTTGTGTAGTTTCTT | 9100 |
| rs549222860 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84725709 | GTGCCCGGCCTGTCT[A/G]ACGACATTTTCAAAC | 9100 |
| rs549244182 | in-del | -/CTGGCTATTTT | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84704714 | TAGATTTTTTCTGAA[-/CTGGCTATTTT]CTGGCTATTTGAAAG | 9100 |
| rs549245428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84749139 | TCATATAGGGCTTAG[A/G]GAGAATGGCATTGTT | 9100 |
| rs549258347 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84703014 | AAAAAAAAAAAAAAA[C/G]AGCGAAACTCCATCT | 9100 |
| rs549277935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84777130 | TGTGATTGTGGGGCC[C/T]GGGAGAAGCAATCTC | 9100 |
| rs549347916 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84716718 | ACTGGGATCTTAGGT[G/T]CACGACCTTCGGCAA | 9100 |
| rs549349158 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84734010 | ATTGAACACACTGCA[A/G]TTTACTTACATATTT | 9100 |
| rs549365380 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84754395 | TATTCTGCGTTTAAC[A/G]ACGTCGTACCAGAAT | 9100 |
| rs549365397 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84749912 | ATTGGCTGTTTTTCA[A/C]GTGTGAACTGTTATT | 9100 |
| rs549384850 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84715226 | TGAGGCACCACTCCC[C/G]GCCCATTTATAAAAT | 9100 |
| rs549387778 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84720990 | CCTCCGCCTGCCGTA[G/T]TCAAGCTATTTTCCT | 9100 |
| rs549424093 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717224 | GTTCTGAAATCATAC[A/G]CAGAAATGTGTGTAC | 9100 |
| rs549426276 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84754023 | CTGAGGACACAAAAG[C/G]CCACCAAGTCCTGTT | 9100 |
| rs549439624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84770009 | AGCACTTTGGGAGGC[C/T]GAGGCAGGAGGATTG | 9100 |
| rs549480604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717319 | CAAAAAAGATTAGGA[A/G]TCCTCCCTTTTAGAA | 9100 |
| rs549509204 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84743978 | TAATTGAAGGTTACC[A/T]GCGGAGGAGACCAAG | 9100 |
| rs549510178 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84735298 | CACACTGATGTAACC[A/G]TACGTTTTAGTTGCT | 9100 |
| rs549542057 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84713196 | ACCATTCACCCACTA[G/T]TTATTTATTGAACTC | 9100 |
| rs549549020 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84706664 | TCCTGCCTCAGCCTC[C/T]GGAGTAGCTGGGAAT | 9100 |
| rs549617059 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84735355 | GTGGATGGGTGGGTA[C/T]CTGTTTGCAAGTGAG | 9100 |
| rs549660255 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84752432 | GTCAAGTTTCAACCT[A/G]GAAGTTGCCTGCCCT | 9100 |
| rs549673583 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84702735 | CGGTGGCTCGTGCCT[C/G]TAATCCCAGCACTTT | 9100 |
| rs549674805 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84761099 | TGGAATTTGCACTTC[A/C]CAAGTAATGGGAACA | 9100 |
| rs549700297 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84757351 | CTACGCTTCTTCAGT[A/T]AGAAGGAAGAGGACA | 9100 |
| rs549758520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84707041 | CTGTCCTGTATTATT[A/G]TAACCATTTTACAGA | 9100 |
| rs549762386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84761642 | AGAGTTTTTACTGAG[A/G]GCTGGTCCCATAGGT | 9100 |
| rs549764767 | in-del | -/G | 0.0123036 | 0.0774623 | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779976 | GTAACTGAAATTCAT[-/G]GGGGGCATGAGTTTG | 9100 |
| rs549773840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84778257 | AGGGTCCCTCCTGCC[A/G]TGTGGGCCGGCACCG | 9100 |
| rs549774627 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84748478 | CAGGCTAATTTTTGT[A/T]TTTTTAGTAGAGACC | 9100 |
| rs549774903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84746231 | CTAAGGCTCCAAAGT[A/G]GAAACAATTCACAAT | 9100 |
| rs549776368 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84737067 | TGCTGGGATTACAGG[C/G]GTGAGCCACCACGCC | 9100 |
| rs549792135 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84719119 | GTTGTTGTTGTTGTT[G/T]TTGCCTTTATTAACT | 9100 |
| rs549800595 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84743370 | AGATTCAGGAGGCCT[C/T]GGGAGGCTGTGTAGC | 9100 |
| rs549830799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84777900 | ATTCCCCGCGGAATG[C/T]TGCCGGACAGCCGCC | 9100 |
| rs549853540 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84715429 | GTGGCAGGTTCTTTT[G/T]TAGTAATTCAGAGAA | 9100 |
| rs549880492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84767148 | CAGAAAAGCTTTTAG[C/T]GAGCTCTTCACCGCA | 9100 |
| rs549900767 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84732706 | GCCCATGTCAGCCTC[C/G]CAGAGTGCTGGGATT | 9100 |
| rs549916830 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84715704 | CACCATAAACTAGAG[A/T]TTTAGTGGCTCATGT | 9100 |
| rs549938667 | snp | A/G | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84761950 | GCACTCACGTGAACA[A/G]CTGCTGTCCACGTCT | 9100 |
| rs549941895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84766712 | ACTTGCTGGCTCAGA[C/T]TGAACAGCTCTGTCA | 9100 |
| rs549955287 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84738041 | CACCCCGTGGTTGAA[C/T]GTTGAGGAAGGGGAC | 9100 |
| rs550055742 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84728848 | CTGTCATTCAGGCTG[A/C/G]AGTGTAGTGGCACCA | 9100 |
| rs550085237 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84771681 | CAAGACCAGCCTGGC[C/G]AACATGGTGAAACCC | 9100 |
| rs550091012 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84729047 | AAGTGATCTGCTCGC[C/G]TCGGCTTCTGGAAGT | 9100 |
| rs550101310 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741066 | CCTTACTGGCCTCCA[C/G]GAAACTGATGCCAAA | 9100 |
| rs550115838 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84765695 | GACAGTTGTTTCCCT[C/G]TCTTGGCTGTTGTGA | 9100 |
| rs550116046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84770735 | CGAGATAGCGCCACT[A/G]CAGTCCGGCCTGGGC | 9100 |
| rs550122122 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84711909 | ATTTTTAGCAGAGAC[A/G]GGGTTTCACCATGTT | 9100 |
| rs550138116 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84759140 | TGGTTAGGTCAAGTT[A/C]TTGAATACAAACGAC | 9100 |
| rs550138395 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84734353 | ACTCTCATTGTTTTA[A/T]TTTACATCTCCCAGA | 9100 |
| rs550169856 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84728279 | TAAATAATTGTCACT[C/G]ACTGGTATTTGCTAT | 9100 |
| rs550176119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84734897 | ATTCATTGGGAACTC[A/G]GCCCTTAGCTGTCCT | 9100 |
| rs550392538 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84771204 | AGCATTCATCAGACC[C/T]GTGAAAGTACTTCAG | 9100 |
| rs550395229 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779314 | TGCTTGATTTTAGAA[A/C]ATACACAAAAACCCA | 9100 |
| rs550521440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718751 | ACAGAGCAAGACTGT[C/T]TGACAAAAAAACAAA | 9100 |
| rs550541568 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84729357 | ATTCTTAGGATTCCC[C/G]TAGCTTGTGATATCG | 9100 |
| rs550542170 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84777732 | GCCTCCTGCTGTCAT[G/T]TAGCCCCTCCACGTG | 9100 |
| rs550546637 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84740164 | TAGATTGCACTGACT[C/G]TTCATGTATGTTATT | 9100 |
| rs550564445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84739795 | AGGCACTGTGTTAAA[A/G]AGGGAGCTGCAGTCA | 9100 |
| rs550565821 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84755149 | GGAAGTTTCAGGCAG[A/T]TCTTGTATGCCTGGC | 9100 |
| rs550597471 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84708609 | TCACCTGAATTTTTC[A/T]CCATCTTCTTCAAAA | 9100 |
| rs550597637 | snp | A/C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698079 | TCCAAGTGCAGATAT[A/C/T]GCTTTTCCATGGTTA | 9100 |
| rs550627155 | snp | C/G | 1.66294e-05 | 0.00288347 | intron-variant | USP10 | GRCh38.p7 | 16:84759482 | CAGCTTGTAAGTAAG[C/G]TGGTGAAAGATGTGT | 9100 |
| rs550635316 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84709284 | TCCCGTGGAAGTGAC[G/T]TGTTTACAGCATGAG | 9100 |
| rs550644403 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84703848 | TGCTCTTGAGCCCAT[A/C]TCATTGAGAGCACAG | 9100 |
| rs550652155 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84772213 | CCCACCACCACGCCT[A/G]GCTAATTTTGTATTT | 9100 |
| rs550707192 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698897 | GCTGCGCCTGGCCCA[C/G]TTATATTTTTCATGG | 9100 |
| rs550716880 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84775545 | CTGTGCTTGTGGCAC[A/C]TGTGGGTGACAGTGC | 9100 |
| rs550733779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751494 | TGGCACCTGTTTACC[A/G]GGATCCACCCTTGTG | 9100 |
| rs550753142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84716164 | ACTGTCCCACATGAG[C/T]GTAATGTCTCTCCCC | 9100 |
| rs550755032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84720623 | GCCTCGCTGTGTTGC[C/T]CAGGCTGGAGTGCAG | 9100 |
| rs550764882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84724845 | GCATTCACTAGTTGA[C/T]GATAGTGTCATCTCC | 9100 |
| rs550821999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84756174 | CACAGTTCGTCCCTT[C/T]ACTGGTCTGCGAGCT | 9100 |
| rs550925378 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84717118 | CTGTGCGCTGTCTGA[C/G]CTCCTAGGTAATTCC | 9100 |
| rs550949585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84761566 | TAACTACTCCAGCAC[C/T]AGACTGTGACCACAC | 9100 |
| rs550950935 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84730526 | AAAATAATAGGAGAA[A/G]AAAAACTCAGTGAAC | 9100 |
| rs551012445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84712232 | TCCTTCCTCAGGAGG[C/T]AGTCAGCTGTGTACA | 9100 |
| rs551015962 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84756438 | TCTCTCCTAAAAATA[A/C]AAAAATTAGCCGGGC | 9100 |
| rs551021418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84776277 | CGAGTGGGTGAGGGC[C/T]CAGGGATGGGGGCCC | 9100 |
| rs551074163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84765034 | GAGCCAAGATTACAC[C/T]ACTGCACTCCAGCCT | 9100 |
| rs551137449 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84764664 | GGTGAAACCCCGTCT[C/G]TACTAAAAATACAAA | 9100 |
| rs551155647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84714057 | GGGCACCAGAATAGT[A/G]AGGTTCAGTTGAGAG | 9100 |
| rs551178374 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84704058 | ATGCCAAGCCTAAGC[A/G]GCACGTTGCACTGTG | 9100 |
| rs551206879 | snp | C/G | 4.99322e-05 | 0.00499636 | intron-variant | USP10 | GRCh38.p7 | 16:84759841 | AGCTCTTTAGTAAAA[C/G]TATATATTGTTTAAA | 9100 |
| rs551217483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84714661 | TTGGCAGGTTTTTTT[A/G]GTCCAATTTTTAGTT | 9100 |
| rs551250988 | snp | A/G | 0.000283336 | 0.0118991 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764125 | AAAACCACTCGGTCA[A/G]TGAAGAAGAGCAGGA | 9100 |
| rs551280065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718650 | TAATACCAGCTACTC[A/G]GAGGCTGAGGCAGGA | 9100 |
| rs551282853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84710426 | AAGCCTCATAACTTT[A/G]AGGGGAAAGAAGTAG | 9100 |
| rs551310589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741087 | TGATGCCAAACTTTT[C/T]CTTTGAGAGTTAGAG | 9100 |
| rs551314341 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84763861 | CCATGGATCCAGTGA[C/T]GTTGCACCTGTTGCG | 9100 |
| rs551324890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84769607 | ACTGTCGGCTTGGCT[C/T]ACTTCTGTGGCAGCT | 9100 |
| rs551388524 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84773629 | CCGGGTTTAGTGTCC[A/G]TTGCTCCTCTCACAC | 9100 |
| rs551400093 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84727331 | AAACACCTACAATTT[C/T]CCCCCCTCATGTGAC | 9100 |
| rs551448595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84744492 | TTTTCCGCAAATTGT[C/T]CAGCGTAAGTAAAGG | 9100 |
| rs551461090 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84774684 | ACTGTATTAGCCAGG[A/G]TGGTCTCGATCTCCT | 9100 |
| rs551489288 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84702819 | CCAATATAGTGAGAC[C/T]CTGTCTCTACTAAAA | 9100 |
| rs551522812 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84777808 | TGAAATTCCCTACCA[G/T]CCAAGTCTTGCATCT | 9100 |
| rs551522880 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84774510 | TTTTCTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 9100 |
| rs551537760 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84713699 | GGTGTGGGAAAGAAG[C/G]TAGAGAATCAACTGT | 9100 |
| rs551562409 | snp | C/G | 1.6989e-05 | 0.00291449 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745142 | ACAGACTCTGTCAGT[C/G]ACATTGTGCCTGACA | 9100 |
| rs551571453 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84740194 | TCTGCTAGAAGTAAC[A/G]GCATGCAAAGTTGTA | 9100 |
| rs551573648 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84735268 | AGTAAGGGGATTTTG[C/T]ATTTTTTCCCACATC | 9100 |
| rs551592443 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP10 | GRCh38.p7 | 16:84773943 | TGCCACCTCCAATAC[A/G]TTATCAAAATATGAC | 9100 |
| rs551604268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84709140 | GGCATTGTTTCTCTC[A/G]CGGAGGAGTTTATGG | 9100 |
| rs551624637 | snp | C/G | 1.80338e-05 | 0.00300276 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745546 | GCCCTCTTCCTCCTC[C/G]CCGGTGGCCTATGTG | 9100 |
| rs551664663 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84738199 | CAGCATTCTCTCTTC[A/C]CCGAGCAGAACAGAA | 9100 |
| rs551665372 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84700451 | GGCCCTCCCCGCCGC[C/G]CCGGCCGGGGGAGGC | 9100 |
| rs551700707 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84700824 | GGCCCTTTACAATAA[C/T]CCCGTGGTGGAAAGA | 9100 |
| rs551714802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84746630 | CACTCACCGTGAATG[A/G]AGCTTGCAAGACTGG | 9100 |
| rs551729554 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84766135 | GTCTCAGTTCTGAGA[A/C]TGAATCAACAACTTT | 9100 |
| rs551776200 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84742230 | TAGATGTTCCTAAAG[C/T]TTGAGATACCACTCC | 9100 |
| rs551793014 | snp | C/G | 0.0298908 | 0.118541 | intron-variant | USP10 | GRCh38.p7 | 16:84770763 | GGCGACAGAGCGAGA[C/G]TCCGTCCCCAAAAAA | 9100 |
| rs551822105 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84726819 | GTACTTTGCTCCCCC[G/T]AATCGCAGGCATTTC | 9100 |
| rs551869190 | snp | A/C | 0.00199481 | 0.0315187 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699681 | CCTCAGCCCGCGACT[A/C]CCGGGCTCCGGGGGC | 9100 |
| rs551889120 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84750703 | TGTATTTGATGTTTT[C/G]CTTTCAAAATTATGC | 9100 |
| rs551899979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84740550 | GAATTGGTTTTAAAG[C/T]GTATCCTGTGCTTCG | 9100 |
| rs551921297 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84713533 | TCCTTGAGGCCCCAA[C/T]GTAAGCTCCGTGAGG | 9100 |
| rs551951354 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84773651 | CTCTCACACTTCTAG[C/T]TGCCTTATCACTCAT | 9100 |
| rs551996137 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84705152 | ACTCTATGGCTCAGG[A/C]GTCTCAAAACCAGTC | 9100 |
| rs552015162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84736596 | TCGTAATCCTGTTAT[C/T]TATGTTCAGAAAGAA | 9100 |
| rs552016221 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84753193 | ACTGTGTGGCCCAGG[C/G]TGATCTTGGAACTCC | 9100 |
| rs552034302 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84738919 | TCTGAACTTTGCGGC[C/G]CTAGGGCCGTTCCTG | 9100 |
| rs552062050 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698193 | ATATAGCACTACTTA[C/G]AGCCAACAATAGTAA | 9100 |
| rs552077532 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84717019 | TAGAGCATAGCAGTG[C/G/T]TTCTCAAACTTAAAA | 9100 |
| rs552099505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84734388 | AAACAGCTGGGTACT[A/G]TTTCATTCTCTTCAC | 9100 |
| rs552142348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84732315 | AACCACACTCTGCTT[A/G]CCATTTTTATACCCA | 9100 |
| rs552165355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84732751 | CTGCGCCAGGCCTCA[A/G]TGACTTGTTTCTTGA | 9100 |
| rs552188939 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84715457 | GAATGAAGATGGGTA[A/G]TGAGCTAGTCTTGAG | 9100 |
| rs552206609 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84759547 | ATTGAAATAGTTTAG[G/T]AAAGCTCTTGATTTC | 9100 |
| rs552222974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84727916 | TTTTGGGAGTTGACC[A/G]TATAATGTCCTTTCT | 9100 |
| rs552227924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84778757 | GCATTGGTTTGTGTG[A/G]TGACATCTCTCTGTC | 9100 |
| rs552231720 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84738525 | AGACCCACCTCTCTG[C/T]TCCAGGTGCCTGCCA | 9100 |
| rs552238215 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84775000 | ATGGCTCATTTCCTT[C/T]ATGAGTCAATTTTTG | 9100 |
| rs552278347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84754455 | GGAAAGCTTGGTGGA[A/G]TACATTTCCTAGTAC | 9100 |
| rs552286155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84728317 | TTGAATAAATTGAAT[A/G]AATAATTGAAATATA | 9100 |
| rs552290619 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84778344 | GTTTTCTCATTTAAT[A/G/T]TACCATAAGCGTATT | 9100 |
| rs552309433 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84771656 | GGTGGATCACCTGAG[G/T]TCAGGAGTTCAAGAC | 9100 |
| rs552334938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84706561 | ATATATATTTTTTGA[A/G]ACGAAGTCTTCCTCT | 9100 |
| rs552337384 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84763190 | CCCCTCAGTCGTTTT[A/C]CTTTCAAATAGCATT | 9100 |
| rs552393247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84758494 | CCCCCCAGGAAGATT[A/G]AATGTTGCTATTTGA | 9100 |
| rs552448045 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84746292 | GTTTTTAAAAAGTTA[C/G/T]AGTAGGAAGTCAGAA | 9100 |
| rs552469668 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84729495 | TTGTATTGACACATA[G/T]GAAAAAGATACATGT | 9100 |
| rs552472283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84767930 | GGACCCTGCGGCCTT[C/T]CGCAGTGTTTGTGTC | 9100 |
| rs552516651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84762040 | TTGCAGGGCCTTGGA[A/G]TAGGCAGTTGTGCTG | 9100 |
| rs552534795 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84755223 | GGAATGAACATGTTC[A/T]AGCCCCGTCTCACCC | 9100 |
| rs552540197 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84731446 | GCCGTGTGTTTCTTG[-/T]TATTTTACTTCTTTA | 9100 |
| rs552552112 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84724219 | AATACAGTTCTAATA[C/T]AGACACAGGACTGGA | 9100 |
| rs552630185 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84712919 | TTCACCAGAGTTACC[A/G]GCAAGTGCTTGGCTG | 9100 |
| rs552708767 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84707681 | AATGAAGCAGATATT[C/G]TGGAGATTGAAGTGA | 9100 |
| rs552718272 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84743301 | TGGGGCAGGATTGTG[C/G]TGCCACCACCCTTCA | 9100 |
| rs552787805 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84727696 | GACATGGGCTAACAA[A/G]TGCAAATATACAGAC | 9100 |
| rs552793931 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719209 | GATGTTGTTCATCAA[C/G]TTTATATAGTGAGTA | 9100 |
| rs552804820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84763661 | AGGAGTTTATGTAAA[C/T]AAGGATCCAGTGGTG | 9100 |
| rs552840797 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84739991 | GTCACTGACATCCTG[G/T]GGAAAGAAGGATGTA | 9100 |
| rs552866098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84768170 | GGTCTCTTAATTTTT[C/T]TGTTTTTGCTTTCAA | 9100 |
| rs552942535 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84743333 | CCCCCACAGTCGGGG[G/T]CTGTGATTCTAAAGC | 9100 |
| rs552981676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84763914 | ACATTGTGCCTGTTG[C/T]GATTGGCCGTGGATC | 9100 |
| rs552987099 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84755424 | TGGCTGAGCAGCCTG[A/C]ACTTGCTGTCTTCAC | 9100 |
| rs552987198 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84760025 | AATTTGGTAAATTCA[A/G]TCTTGTTGGGAAGAT | 9100 |
| rs552993087 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84758238 | AGCCATTGAACACAC[A/G]CAGTGATGTGTAGGG | 9100 |
| rs553002767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84711610 | GGTTCTCTGTTGCTT[C/T]TTACCTCTTTGCTCT | 9100 |
| rs553066238 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84711989 | CCTCCCAATGTACTG[C/G]GGTTACAGGCATGAG | 9100 |
| rs553066989 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84740643 | TTCTGAGTGCAACAG[C/G]TATGTTACTCTTCAT | 9100 |
| rs553125602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84769262 | ATCTATCCTTGGCTT[A/G]TCTTGTGTGCTCTGA | 9100 |
| rs553131284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84707895 | ACCAGCCTGGGCAAC[A/G]TAGCAAAACTCTTTC | 9100 |
| rs553203295 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84770944 | GGTGGTGTGCACATG[C/T]AGTCCCAGCCTCTCA | 9100 |
| rs553216441 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84703270 | GGTAATTAATTTGAA[G/T]CTATTAGTTTTGCCT | 9100 |
| rs553220921 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84773356 | AAGCAGAAAAGAGGA[C/T]ACTGGGCCTCACTCC | 9100 |
| rs553235505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84729638 | CTGACTTCTTAGCCC[A/G]TTCCTTTATTTCAGT | 9100 |
| rs553248431 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84739110 | GTTGCCCAGGCTGGA[C/G]TGCAGTGGCACTATC | 9100 |
| rs553263457 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84712920 | TCACCAGAGTTACCA[C/G/T]CAAGTGCTTGGCTGT | 9100 |
| rs553271654 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84747296 | CACCTGACACCCTTC[A/C]TTACCAGGATGTAGC | 9100 |
| rs553287042 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84747996 | TCTCTACTAAAAAAA[A/C]CCTAAAAATCAGCCA | 9100 |
| rs553308536 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84737372 | GTATTCTTACAAATA[A/G]TTATATAGTTAATGA | 9100 |
| rs553334183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84703463 | ATTTTACATGATGGA[A/G]AGTCTTGGATTCCCC | 9100 |
| rs553369685 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780086 | AGTATTTTCAAATGG[A/T]TTAGTGATTTGGGTA | 9100 |
| rs553390684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84716192 | CCCCCTCTCCTTTTC[C/T]AGATATGCCAGTTCC | 9100 |
| rs553403199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84709742 | ACGTCTCTTGTAGAA[C/T]GGTGACATTTGAGCT | 9100 |
| rs553427387 | snp | A/T | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84738808 | TGCTGTGATTATTGA[A/T]TTGGTGTGCTGAGAT | 9100 |
| rs553436290 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84742451 | TCTGAGCAGGGCCCT[G/T]GTGTCACTAATCTCT | 9100 |
| rs553449514 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | USP10 | GRCh38.p7 | 16:84707380 | AAAGTCGTTTATTTT[A/T]TTTTCTAGTATAAAG | 9100 |
| rs553464125 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84748490 | TGTATTTTTAGTAGA[G/T]ACCGAGTTTCACCAT | 9100 |
| rs553464386 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84705482 | ACGATCCGCCCACCT[C/T]GGCCTCCCAAAGTGC | 9100 |
| rs553525486 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84752051 | AAAAAGGCTATTAAG[C/G]AACTCCATTTTTCTG | 9100 |
| rs553529723 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84705820 | TACCTCCCAGATTCA[A/T]GCGATTCTCCTGCCT | 9100 |
| rs553533909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84756642 | GGCTTTGAGTCTTAA[A/G]GTTAGGTTTAAAAAA | 9100 |
| rs553547142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84748933 | CAAACAGATTATTTT[C/T]TTAATCCTATTTGGT | 9100 |
| rs553563085 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84776430 | TCTTCTTTTCTCCCC[C/G]CGATCACAATTCCTC | 9100 |
| rs553579873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84736848 | GGCTGGACTGCAGGG[A/G]CGTGATCTCGGCTCA | 9100 |
| rs553579890 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718630 | GACATCGTGGCACAT[G/T]CCTGTAATACCAGCT | 9100 |
| rs553613474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84734999 | GTATAAACACCACAC[A/G]TTTTATTTTATTTTT | 9100 |
| rs553626769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84727659 | AAATACACACTCATA[C/T]GGATACACATACAGA | 9100 |
| rs553663213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84760379 | TCTGTCTCCAGCGCT[A/G]TAAGTAGATGTAGGT | 9100 |
| rs553666393 | in-del | -/TTT | | | intron-variant | USP10 | GRCh38.p7 | 16:84739063 | TTTCTTCCTAAACCT[-/TTT]TTTTTTTTTTTTTGA | 9100 |
| rs553690090 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84722842 | ATTACAGGTGTGAGC[C/G]ACTGCGTCCGGCTCA | 9100 |
| rs553706103 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84740256 | AATTAAATGGTAAGC[A/G]TTGGTTTTAACATTT | 9100 |
| rs553721631 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84755783 | AGCCTGGGCGGCAGA[G/T]TGAGACTGTCTCAAA | 9100 |
| rs553725078 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84749227 | AAAACATACTCAGTT[C/T]GTTACAAGTCAGATC | 9100 |
| rs553727400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84713819 | CCTTTGGAACTGAGT[C/T]CTATAGTTTGCAGAG | 9100 |
| rs553749726 | snp | C/T | 0.000804991 | 0.0200461 | intron-variant | USP10 | GRCh38.p7 | 16:84777208 | TGCAGGTGTGAGTGA[C/T]ACACGGCTCAGCCCA | 9100 |
| rs553761022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84732815 | GCCAGACTCACATCC[A/G]TGCAGTTTAACCACT | 9100 |
| rs553783458 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84701643 | GCTCACTTCCTTTAT[G/T]TAATAAGCATCAATC | 9100 |
| rs553831875 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84740828 | GCTGACTCTTGGGAA[A/C]TCAGGTCAACTCTTC | 9100 |
| rs553832171 | snp | A/G | 1.70746e-05 | 0.00292182 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745157 | GACATTGTGCCTGAC[A/G]GTCCTTTCCCCGGAG | 9100 |
| rs553834785 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84735565 | TGCAGAATGCTTATT[C/G]ACGTCACAGAAATGT | 9100 |
| rs553857201 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84704523 | GACTGCAGTTTTCCT[C/G]TTTATTGAAGTGTTC | 9100 |
| rs553886430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84737206 | ACATGACCTTCCTAT[A/G]GCCACGGGCCCAGGT | 9100 |
| rs553898690 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741139 | AGCATGGTCAGACTT[A/C]TGAAAGGGGTTTTAA | 9100 |
| rs553916879 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84748572 | GCCTCTCAAAGTGCT[C/G]AGATTACAGGCGTGA | 9100 |
| rs553949129 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84732497 | TGTCGCCCCGGCTGG[G/T]GTGCGGTGGCGCGAT | 9100 |
| rs554038804 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | USP10 | GRCh38.p7 | 16:84774546 | CGCGATCTCGGCTCG[C/T]TGCAACCTCTGCCTC | 9100 |
| rs554040807 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84770189 | ATGCTGCCAGCCGTT[C/G]TGGGTGCGTGGTTGT | 9100 |
| rs554076107 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84734267 | TCTTGCTCGTATTAA[A/G]AAAAAAATCTTGCTA | 9100 |
| rs554103882 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84765425 | CCGACATCTTCCATT[A/C]CCACTCGCCACCCCT | 9100 |
| rs554153861 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84736050 | CTTGGACCTGTGGGT[G/T]TGTGAGTGGCGAGGG | 9100 |
| rs554185311 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84709155 | GCGGAGGAGTTTATG[C/G]GTCCATTGAGGAAGA | 9100 |
| rs554193227 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84753547 | GGTGCAGCTCCTTAC[C/G]TGTTCCAGGTGCGGA | 9100 |
| rs554231983 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84722258 | TTAGATTTAGCCATG[A/T]TGAGTGTTGAGTTCC | 9100 |
| rs554245819 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699960 | CGGCCTCCCCGCGCC[C/T]CGCGGCGCGCGGCCA | 9100 |
| rs554252013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84761758 | GTTTAGGCAGAATCC[C/T]GTATCAGTTATTGGA | 9100 |
| rs554308265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84703030 | AGCGAAACTCCATCT[C/T]AAAATAAATAAAAAA | 9100 |
| rs554313158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84765958 | GAAGGTTTACCCATC[A/G]AAAGTACTGAAGAGG | 9100 |
| rs554341437 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84776406 | ACTATTCATTGTTCC[C/T]TTTGACTCTCTTCTT | 9100 |
| rs554344873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84729185 | ATGATTTTGTTAAAT[A/G]CAAAAATGATGTCTT | 9100 |
| rs554354665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84726540 | CTTAGCCAACAGGCT[A/G]TGCTTCAGGGAGGAA | 9100 |
| rs554374534 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84732224 | TGTAATATTTAGTTA[C/G]TGGTTATTTTTGAAT | 9100 |
| rs554396710 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751061 | ATGTTTCAGTCAACA[A/G/T]CAGACCGCATGTACG | 9100 |
| rs554410255 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84728305 | GCTATAAATATATTG[A/G]ATAAATTGAATAAAT | 9100 |
| rs554424445 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84711563 | TTCTAGTCTCTAGTT[G/T]TTCCCAAACTGGTGC | 9100 |
| rs554453735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84758278 | GATGCTGGGGATGCA[A/G]AGAGGAATGAGACGT | 9100 |
| rs554505481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84733539 | AGTGAGTCCGTGGGT[A/G]GATACAATTAATAGT | 9100 |
| rs554511210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84772428 | CATGAAGTCCTGCCA[C/T]AGGACTCTTGGGCCT | 9100 |
| rs554521841 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84762849 | TGCAAGGGAAACCCA[A/T]GTCATCATGTCATTG | 9100 |
| rs554526103 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84702433 | TATGACAGGATTTAG[G/T]TACTGGTTCCTGCTC | 9100 |
| rs554603274 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751336 | TATCCTAAAACTGAT[C/G]TTTATTTTGGCAGTT | 9100 |
| rs554656853 | in-del | -/A | | | intron-variant | USP10 | GRCh38.p7 | 16:84761977 | GTCTACTATCTGGAG[-/A]GGGCAAGTAAACTTT | 9100 |
| rs554668450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84755270 | CCCTAACTCTGCCCT[A/G]GAAGACCTTTCCTTC | 9100 |
| rs554696122 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84775618 | GAGCGCGCCCCCAGC[C/T]GGTGATCCCTGCGTC | 9100 |
| rs554700534 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84771390 | GTCCCAGCTACTTGG[C/G]AGGCTGAGGTGGGAG | 9100 |
| rs554702640 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84749439 | CTTTTGGGAAAGAGG[A/G]AGTAGGGAATGATTT | 9100 |
| rs554716774 | snp | C/T | 0.000866898 | 0.0208014 | intron-variant | USP10 | GRCh38.p7 | 16:84733424 | TCAGTGACTCTCTTA[C/T]TTTTTTTCAGTATAT | 9100 |
| rs554727798 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84754955 | AGACCAGCCTGGCCA[A/G]TGTGGCAAAACCCTG | 9100 |
| rs554736758 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84714837 | TATTTAAAACATGAA[-/T]TTTTTTTAAATTTTA | 9100 |
| rs554743409 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84724631 | ACTTCTCTTCCTCCT[C/T]CTTCCTTTGTCTGCT | 9100 |
| rs554761337 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779555 | CAAAGAAGAACTAGT[A/T]CTTACTTCAAAAGAA | 9100 |
| rs554772103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84770895 | ACATGTTGAAACCCC[A/G]TCTCTACTAAAAATA | 9100 |
| rs554813976 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84715921 | GCTTCACATTTGGGC[A/T]CAGCCTCCGTCACAC | 9100 |
| rs554833633 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84774773 | CGTGCCTGGCCTGTA[A/G]TTGAAGTTTTATGAT | 9100 |
| rs554847237 | snp | C/G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84755157 | CAGGCAGATCTTGTA[C/G/T]GCCTGGCCCTGGTGG | 9100 |
| rs554863793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84715510 | CAAAGTGCTGGGATT[A/G]CAGGCATGAGCCAGT | 9100 |
| rs554899131 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84776036 | CTGTTTGTATCGTAA[C/G]ATAACACTGCCATTT | 9100 |
| rs554926351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84754252 | AGAGATTAATAACAG[A/G]ATGATACGGTATTTT | 9100 |
| rs554944397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84721055 | CCCGCCACCATGCCT[A/G]ACTAATTTTTGTATT | 9100 |
| rs554964912 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780156 | GTTTTCTCCCCTTCC[C/T]CTCCTCATCCCTTGT | 9100 |
| rs555008793 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84747001 | AGACACAAACATTAG[C/T]CTGGGCCTGCACAGG | 9100 |
| rs555071536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717496 | ACTGCTTTTTAATGT[C/T]CTTTTTATGTCATTG | 9100 |
| rs555123972 | in-del | -/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84739260 | AGACAGGGTTTGTTT[-/G]TTTTTTTGTTTTGTT | 9100 |
| rs555167946 | snp | C/T | 1.65721e-05 | 0.0028785 | intron-variant | USP10 | GRCh38.p7 | 16:84740385 | GTAAGCTAGTTCTCT[C/T]CTTATTTCCCTGAAG | 9100 |
| rs555184199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84768708 | TACCGTAGGGTACAA[C/T]TGTCATTAGATTAGT | 9100 |
| rs555186483 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84760064 | TACACCTATGCCATT[C/G]TCAACATTCAGCCAG | 9100 |
| rs555191683 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84755610 | CACTGCACTCCAGCC[C/T]GGGTAATAGAGCAAG | 9100 |
| rs555228494 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84753323 | AAGATTTTAAGGAAG[A/T]TGGGCTAACATTTCC | 9100 |
| rs555247504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84772922 | ACTAGATTAGAAAAA[C/T]AGCAGCTTTTGTCTA | 9100 |
| rs555250130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84763929 | CGATTGGCCGTGGAT[C/T]CAGTGACGTTGCTCC | 9100 |
| rs555252889 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84711172 | AAGTCCATGATTATG[C/T]CTTTTAAGCAAGCAT | 9100 |
| rs555375071 | in-del | -/TC | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84758388 | GGAAGAAAGGCTGTA[-/TC]TCTCAAATCTATTCT | 9100 |
| rs555390166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751777 | CCAGAATGTCGATTA[C/T]GGGCCAGTTATTGAG | 9100 |
| rs555398210 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84771312 | ATCCCAGCACGGTGG[A/G]AGACTGAGGCGAGCA | 9100 |
| rs555398639 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84709567 | GAATAGACTCACGGG[G/T]TCGCAGTGGCCATAA | 9100 |
| rs555403454 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84708030 | TTGTAGTGAGTCGAG[A/T]TTGTGCCACTGCACT | 9100 |
| rs555452002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84760872 | CCCAGATTGAGTTTG[C/T]GATGAATCAGTACAA | 9100 |
| rs555453546 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84755946 | ATCTGTTGTATTCCT[A/C]CTCTAGTTGGATAGC | 9100 |
| rs555463227 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84703514 | TTACTGTATTGCTGA[A/T]TATCTGTTTCTAGCC | 9100 |
| rs555466924 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84708374 | AGAATAGCTTGAACC[C/T]GTGGGGGCAGAGGTT | 9100 |
| rs555501646 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84744214 | GCTGATTTAACCATG[A/T]TTTAAGTCCCTAAGT | 9100 |
| rs555528001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84713362 | TGGGCCATCTTCTTA[C/T]ACCCACTTTACCCAC | 9100 |
| rs555597417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84709199 | AGATAATCACAGTTA[C/T]GTACACGTCACTCCA | 9100 |
| rs555696360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84730094 | AAACCCTCCAAAAAA[C/T]GTGCTAGGAAATCCC | 9100 |
| rs555703443 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84770568 | ACGAGGTCAGGAGAT[C/G]GAGACCATCCTGGCT | 9100 |
| rs555731325 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699033 | CTGTAGGTGTTTGTT[A/G]AATAAATGAAACCAA | 9100 |
| rs555753913 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84749007 | AGTTTCTTTAAAAAT[A/G]TATAATTCTTTTCAG | 9100 |
| rs555759637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84743127 | GAACAGCCAGCCCCT[A/G]CATATGATAATAAAT | 9100 |
| rs555776183 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84702400 | AGAATAGTAATGCAA[A/G]CAAGTAATGGAATCA | 9100 |
| rs555777419 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84765228 | CTACAGTGAAGCAGA[C/T]AAACATATTCCCCAT | 9100 |
| rs555792503 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84767701 | TTCCAGAGCACTGGC[A/G]TTGGGAACATTTATC | 9100 |
| rs555803278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84749677 | TGGACTATTTCCCCT[A/G]TTGTTAAGTCTGCTT | 9100 |
| rs555818721 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84734718 | GGAAATTCTTCCCAT[A/C]CTTTAGATAACGAAG | 9100 |
| rs555826281 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84739125 | GTGCAGTGGCACTAT[C/G]TCGGCTCACTGCAAG | 9100 |
| rs555840745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84764788 | GTGGCCCAGATAGCG[C/T]CATTGCACTCCAGCA | 9100 |
| rs555849279 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745651 | TCCGGTTTCAGAGGA[C/T]CCTGTAGCCATAAAG | 9100 |
| rs555852875 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717830 | ATGTGATTTCAGTAC[A/G]GATTAATTTACTGTA | 9100 |
| rs555866604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84753385 | AGACTCTCACATAAA[C/T]TCATTTGCTTTTCCC | 9100 |
| rs555866762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84749257 | CCACTACCACAAATT[C/T]CCTTTAGTGGGCACA | 9100 |
| rs555903857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84769761 | GCTGCCTAGGGAAGA[C/T]CCTTTTGTGATGTGT | 9100 |
| rs555948872 | snp | C/G/T | 0.00159649 | 0.0282165 | intron-variant | USP10 | GRCh38.p7 | 16:84735048 | TTCTTTTCTTTTTTT[C/G/T]GAGACAGGGTCTCAC | 9100 |
| rs555956342 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84776830 | AACCCATTATTTTTT[G/T]GAGATAGAGTTTTGC | 9100 |
| rs555976201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84774322 | TACAGATGGCTGCCT[C/T]GAACAGCATGCCTCC | 9100 |
| rs555989417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84702247 | ATTTTTATTAAAGAC[A/G]GGTTTCACCATGTTG | 9100 |
| rs556009854 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84731958 | AGTATTTCAGAAGAT[C/G]ATTTCTGAACCATTT | 9100 |
| rs556027703 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699451 | TTATGCCCTACGTTT[C/T]GTTTTTGTCTGTTTT | 9100 |
| rs556037443 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84777256 | GCTGCTTATGAAACT[A/C]GAATGGTGACATGCA | 9100 |
| rs556078300 | snp | C/G | 0.000203352 | 0.0100814 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745597 | CGCCATATCTCCCCT[C/G]GTTTCTGAAAAGCAG | 9100 |
| rs556085662 | snp | A/T | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84741173 | CAATTTAGGCTTCAA[A/T]AGAAGCCTTGAAAAG | 9100 |
| rs556120334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84710126 | AATACAAAAATTAGC[C/T]GGGCGTGGTGGCGCA | 9100 |
| rs556150915 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84774614 | TAGCTGAGACTACAG[C/G]CGCGTGCCACCACGC | 9100 |
| rs556152262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84778150 | ATAGAAAAATGGGTA[A/G]TTTTTTTTAAAGGCA | 9100 |
| rs556164035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84728408 | TCAGTGGTGCGATCT[C/T]GGCTCACTGCAACCT | 9100 |
| rs556197048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84756719 | CATGCTGGAGTTTTC[A/G]TTTGAGACACTATGC | 9100 |
| rs556283601 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84737644 | TGTCATCTGGGAGTT[G/T]GCTGGTGGTCGTCTC | 9100 |
| rs556308001 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84704976 | GTGGAGTGCGGGCCC[A/G]GCACCTGCTACCGTC | 9100 |
| rs556339620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84728014 | GCTTTTTGTAGTCTG[A/G]AAGTTTCCCACAGCC | 9100 |
| rs556347153 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84732872 | ATTCCGTGAAATCAG[G/T]CTTGCAACAAGGGCT | 9100 |
| rs556402810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84723540 | ATTGCTATGTAGTTT[A/G]GAGAAATTATTCCTT | 9100 |
| rs556407900 | snp | C/G/T | 0.000333575 | 0.0129105 | intron-variant | USP10 | GRCh38.p7 | 16:84733416 | TTATGTGATCAGTGA[C/G/T]TCTCTTATTTTTTTT | 9100 |
| rs556408677 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84760767 | AAAGGCATGAGACCA[A/G]GGGGCCAGGGAGCCC | 9100 |
| rs556427058 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84747333 | CTGCCAAATGCACAC[C/T]CTTCGATGGATGGTC | 9100 |
| rs556435497 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84761281 | TGGGTGCTCAGGAAC[C/T]CCTCTTGGATCGTGC | 9100 |
| rs556446471 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84716542 | GAATTACTATGAAAT[A/G]TGAACAGTGCTTTGG | 9100 |
| rs556516719 | snp | C/T | 5.00113e-05 | 0.00500031 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744876 | GTTCTAATGTGGAGG[C/T]GGAAGTTTTGGAAAA | 9100 |
| rs556523083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84761832 | AAGGGGCAACCTTGC[A/G]AGCAGGCCTTTCCAA | 9100 |
| rs556548584 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84729580 | CTAATCAAGTTCCCC[A/G]GGAGGCTGAGCGCCT | 9100 |
| rs556583918 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84700039 | ATGGCGGCGGCGGGG[A/G]AAGCAGCGTGAGCAG | 9100 |
| rs556584215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84770826 | TAATCCCAGCATTTT[C/T]GGAGGCTGAGGCAGG | 9100 |
| rs556585543 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84705270 | GGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG | 9100 |
| rs556628733 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84710034 | CAGCACTTTGGGAGA[C/G]CGAAGTAGACGGATC | 9100 |
| rs556646622 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84754288 | ATGAAAGACTTGCCA[C/G]TAGATAAAATTTTTC | 9100 |
| rs556693108 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84762203 | AGTGGAGTTTTTCCA[C/G]ATGTAGTTTGAGTTC | 9100 |
| rs556711075 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84774016 | GCACTTTGGGAGGCC[A/G]AGGCAGGCAGATCAC | 9100 |
| rs556751510 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84725004 | TTTTATTTTGATATA[A/C]GTACTGACCTTTTTT | 9100 |
| rs556798050 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718201 | ATGAGAGATGAGTTT[A/G]ATTACAAAAGAAATG | 9100 |
| rs556815814 | snp | A/G | 0.00031412 | 0.0125284 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745220 | CCAGAGGGGGGCCCC[A/G]GGGCTGATTTTGGTC | 9100 |
| rs556844325 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84714321 | TGTTTTTCCCACTTC[G/T]TCCTCTTTTTTAGAG | 9100 |
| rs556904529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84775310 | TTTGCTGCAACTTAG[C/T]ATAGCGACCAGATGC | 9100 |
| rs556929417 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84772209 | GGCGCCCACCACCAC[A/G]CCTGGCTAATTTTGT | 9100 |
| rs556942055 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719329 | TAGTTTCTCCCACCT[A/C]CTCAGTTGCCTGTAG | 9100 |
| rs556979083 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84703410 | CTGCATAGACTCACC[A/C]CAGTCTCTTTTTTAG | 9100 |
| rs557001318 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719685 | CTAGTGTATGTAGGT[A/C]CCATAAGGGGGACTT | 9100 |
| rs557003327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84715596 | AACTATCCTTTTATC[C/T]CCCTTTTTGCTTACC | 9100 |
| rs557039281 | in-del | -/CAAA | | | intron-variant | USP10 | GRCh38.p7 | 16:84727487 | AAACAAACAAACAAA[-/CAAA]AACTCTTTATTTGCA | 9100 |
| rs557062447 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, splice-acceptor-variant | USP10 | GRCh38.p7 | 16:84715849 | TTCATTCTGCCTGTC[A/G]GTATTATCCCAGGGC | 9100 |
| rs557093623 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84767361 | AAATGAAATGAAAAA[C/G]CAGCTAAGAAAACAA | 9100 |
| rs557100063 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84741771 | GGGTATCTTGTGTTT[C/T]CATGACATTAGTTTC | 9100 |
| rs557102429 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84773000 | CAGTTTGCCTTCCAC[C/T]GAGTATTAACAGCTG | 9100 |
| rs557123788 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84751318 | TCATTAAGCATGGCT[C/G]TGTATCCTAAAACTG | 9100 |
| rs557123956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751377 | GCATATATTTCCCCC[C/T]GCTCCTTGGGGGAAA | 9100 |
| rs557126234 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84720371 | TGTAGCACTCTGTTT[A/G]ATGAAATACTATAGT | 9100 |
| rs557145646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84771480 | AGCATGGGCAACCAG[A/G]GTGAGATCCTGTCTT | 9100 |
| rs557187706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84716439 | ATTCAGCAAATCTTT[A/G]TTAGATTCTCAGTAT | 9100 |
| rs557209403 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84775047 | GAGTGTTGTTTTGTT[C/T]CTGGTCTGACAGGCA | 9100 |
| rs557222393 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84763690 | TGGTGCACCTGTTGC[A/G]ATTGGTTGCCGTGGA | 9100 |
| rs557235330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84742367 | AAAGCTATTCACAGC[C/T]TTCTCTCCCCTCCCT | 9100 |
| rs557261845 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84772745 | TGCACATCAGAAGCT[C/G]AACCCTGTAGCATTT | 9100 |
| rs557268114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84711537 | GCTCATGGATTCGTC[A/G]GGTGAGGAAATTCTA | 9100 |
| rs557286712 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84773410 | TGAACCGAGAGTCCT[C/G]TTCTCTCCGTCCCCT | 9100 |
| rs557320358 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84750565 | TGACGAACATGTGAC[A/G]TTTGAAATTGAACGT | 9100 |
| rs557388361 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84759642 | GTTAACCAGAAATGG[A/C]ATTGGAGCATTGATG | 9100 |
| rs557389315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84713426 | CCTGTCTGCTTGCTC[C/T]CTCTCCAGAGCACTT | 9100 |
| rs557391525 | in-del | -/AAAG | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84758997 | GTCCATCTCCCTCTA[-/AAAG]AGAGGATATGTTGGC | 9100 |
| rs557425757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741981 | TTATTCTGCTCCCTC[C/T]CACTACCTCCAGCTG | 9100 |
| rs557447525 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84760693 | TTACAGGCTTTAGTA[A/G]CTATTTGATGTACTT | 9100 |
| rs557477188 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84703370 | CCCAATTTGAATGTC[A/G]TGCAGTTGGCTTCTG | 9100 |
| rs557489727 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84746772 | TTTACAAATTTTTCC[G/T]CAATAAGAAATTAAC | 9100 |
| rs557523600 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84752196 | TGTGCCTTTTCTCAC[A/G]CATTGTTCTAGGCAG | 9100 |
| rs557550754 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780025 | GCCCTTCGATCAGCT[C/G]GACGTGTTTGTGGAA | 9100 |
| rs557584177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84756295 | GAAAGGCAGCATGTT[A/G]TTTAACAAAGGTTTC | 9100 |
| rs557679951 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84732455 | TCTTCTTTTTTTTTT[C/T]TTTCTTTTTGAGATG | 9100 |
| rs557754455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84737163 | ACGGAAAGCAGAACA[C/T]ACAGGTAGCCCAGAG | 9100 |
| rs557787082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84705783 | GGAATGCAGTGGTGC[A/G]ATCTGGGTTCACTGC | 9100 |
| rs557827847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84739661 | GCTAGGAAGAAGAAA[A/G]ATTTAAGTTATTTTT | 9100 |
| rs557846396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84757103 | TGAATAATATACACA[A/G]AGCTTCTAGCACAGT | 9100 |
| rs557883673 | snp | C/T | 1.65853e-05 | 0.00287964 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744702 | ACACTTTGCCGAGAA[C/T]CCCCAGCTACAGTAT | 9100 |
| rs557915728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84709621 | TTGGACTTTTGACTC[A/G]GAGGGTGCCGTGGAG | 9100 |
| rs557916884 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84706792 | GGATCTGCCCACCTC[A/G]GCCTCCCAGAGTGCT | 9100 |
| rs557975110 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84705319 | TCACTGCAACTTCTG[A/C]CTCCCGGGTTCAAGT | 9100 |
| rs557991639 | in-del | -/AAATTTTC | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698148 | AATTTTTTGTTATAA[-/AAATTTTC]AAACATAGAGAAAAG | 9100 |
| rs558089178 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741886 | GCAGGATCCATTTCT[C/G]TGTGTCTGTCACTGC | 9100 |
| rs558167290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84773842 | CTTCACTCGCCTCCA[A/G]ATCAGCTGTCTGAGC | 9100 |
| rs558229744 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84761331 | CAAAAGCATCTTCTA[A/C]AGGTTACATTAATAG | 9100 |
| rs558255240 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84729683 | GACCGGTTTTAAATA[A/T]TGCTGAAGTGTAACT | 9100 |
| rs558304678 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84770159 | CATTTTGGTGGACTC[C/T]GGAAGATAAAAAGGA | 9100 |
| rs558324192 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84749734 | ATCAGAAGTGAAATT[A/T]AGAAGGCAGATGGAC | 9100 |
| rs558465417 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84754174 | CTACTGTGGAGACAG[C/T]GTGGAGAATCTTGAG | 9100 |
| rs558496414 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84778568 | AAGGGCATGAGCCAG[A/G]TCTGTAGGCCTGTAC | 9100 |
| rs558523638 | snp | G/T | | | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84716203 | TTTCCAGATATGCCA[G/T]TTCCTCCTGGACTCC | 9100 |
| rs558557757 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84753718 | GACCTTTAAAGTCTG[C/T]TGAGTCATTTCTAAC | 9100 |
| rs558561179 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84770849 | GAGGCAGGCGGATCA[C/G]AAAGTCAAGAGATCG | 9100 |
| rs558610033 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84713355 | CTGTGCCTGGGCCAT[C/G]TTCTTACACCCACTT | 9100 |
| rs558647300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84759166 | ACGACTGACTGCTTC[A/G]TAGATCCTTATATGG | 9100 |
| rs558674818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751025 | GTGTAAATGAACATA[C/T]AGTTATGTGCTGCTT | 9100 |
| rs558683403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84774749 | GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCCT | 9100 |
| rs558711355 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant, intron-variant | USP10 | GRCh38.p7 | 16:84758736 | CTGGAGAATGTAACC[C/T]TAATCCATAAACCAG | 9100 |
| rs558728658 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84723973 | ATTTCTTTTTTTCTT[A/C]AGGTCAGCACCAAGG | 9100 |
| rs558758693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84745772 | ACAATGGCAGATTAC[C/T]TGTGTGTTAATAGCA | 9100 |
| rs558772667 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84762741 | TCAAAAATACAGAAA[G/T]TATAAATAATAAAAA | 9100 |
| rs558787974 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84769964 | CAGAAAGAAGGCGGG[C/T]CAGGTGTGGTGGCTC | 9100 |
| rs558788387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719384 | GGGAATGCCCCTACA[C/T]AGTGATTCTAAACTC | 9100 |
| rs558798288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84729145 | TAATAAATGCTTCTT[C/T]ATTGTAGTGCTTTGA | 9100 |
| rs558810082 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84777658 | GAGTCTGACTGGTGG[C/G]CTCAGTCATAAGCAC | 9100 |
| rs558832971 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84762356 | GTCTTCTATTTTGTT[A/T]ACCCAAGACAGAAAC | 9100 |
| rs558875507 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84738022 | GGAGTTGAGTGAGTG[A/T]TCACACCCCGTGGTT | 9100 |
| rs558880876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718827 | AGAAGGAGTCTTTCT[C/T]TGTCACCCAGGCTGG | 9100 |
| rs558938685 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84708526 | CTAGATTTATGAGAG[G/T]ACAAACTTTTTATTA | 9100 |
| rs558966049 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84750590 | GAACGTATGCTTTCA[C/T]TGAACATTGTACTTT | 9100 |
| rs558974369 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84701033 | ATTGTTGCACACTTT[G/T]AAACCATCTCATTGT | 9100 |
| rs559043446 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718530 | TTGGGAGGCCAAGGC[A/G]GGTGGATCACCTGTC | 9100 |
| rs559091833 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779149 | TCACACTCACTTCCC[A/G]CCTCTCTTTAGTGGC | 9100 |
| rs559101401 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84774788 | ATTGAAGTTTTATGA[C/T]CTGACGCATATGTAA | 9100 |
| rs559129655 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84755064 | CTGTGCAATGCTTTC[C/T]TTTTAAGAGTGGAGT | 9100 |
| rs559152195 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84739707 | CTTTTTACAAAGAAG[G/T]CAGACAGTTCCCATT | 9100 |
| rs559171322 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84741642 | TGGCCCTTTTTCTCC[A/G]TTCTTTACTCTGTTC | 9100 |
| rs559239284 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84773156 | TCTCTGTCAGGTCAC[A/G/T]GGCTCGGCACTTTTT | 9100 |
| rs559253523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84714928 | GATTATTATTATTAT[C/T]ATTATTATTTTTTTT | 9100 |
| rs559310220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84710713 | TTGGAATCATTGGAT[C/T]TAACAGCGTTTTTAG | 9100 |
| rs559311916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84711356 | TGTGGACAGCATGGG[A/G]TCAGCACACTCCCCC | 9100 |
| rs559313304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84720429 | GTCTTTGTGTGGAGT[C/T]TGAGTACATGGTCCG | 9100 |
| rs559337982 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84705238 | TGTTTTTTTTGTTTG[-/T]TTTTTTTTTTTGAGA | 9100 |
| rs559338345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84703610 | GCTGAAGTAAATACA[A/G]TTGTTTGAAATGTTG | 9100 |
| rs559356030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84759769 | CACTAGCTGTTACAG[C/T]ATTGGTTACCTAAAA | 9100 |
| rs559378865 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84753177 | ATAGCAACAGAGTCT[C/G]ACTGTGTGGCCCAGG | 9100 |
| rs559396072 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84750015 | AGGATGTATCTAAAC[A/T]CAAAAGCCCTGTCTT | 9100 |
| rs559396171 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84730120 | ATCCCCTCCACTCCT[C/G]TCTGCGTCCACTCAG | 9100 |
| rs559402876 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698839 | GACTTCAAGTGATCC[G/T]CCCGCCTCGGCCTCC | 9100 |
| rs559410058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84754760 | AAGTCGGTTTATAGT[C/T]GATTTATGTATCCTT | 9100 |
| rs559411983 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84720987 | CAACCTCCGCCTGCC[A/G]TATTCAAGCTATTTT | 9100 |
| rs559417521 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84751778 | CAGAATGTCGATTAC[A/G]GGCCAGTTATTGAGC | 9100 |
| rs559430961 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84749064 | GAACGTAGTTGTTGA[C/G]AGTTTCAGGAGTCTC | 9100 |
| rs559454375 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | USP10 | GRCh38.p7 | 16:84711756 | TGTCTGAGATGGAGT[C/G]TTGTTCTGTCACCCA | 9100 |
| rs559464990 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | USP10 | GRCh38.p7 | 16:84739597 | ACTTTCTTACACCCA[A/G]TGTGTCCATTGGAAG | 9100 |
| rs559520916 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84749087 | GGAGTCTCGTGAGAT[A/G]GTAGAGCAATAGAGT | 9100 |
| rs559535364 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84724226 | TTCTAATATAGACAC[A/T]GGACTGGAAAGTTGG | 9100 |
| rs559541933 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84770488 | AGAAATTAAGCCTCA[A/G]TTGGCTGGGCGAGGT | 9100 |
| rs559547327 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84748193 | GATAGATTGTGTAAG[C/G]CTTTATATAGATTAC | 9100 |
| rs559576378 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84747506 | TGAGCAAATGATAGG[C/T]CAGACGTCGTTATTT | 9100 |
| rs559583911 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84733627 | TGGAGACTAATATGA[G/T]AAATGCCTCAACCCA | 9100 |
| rs559605893 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84702630 | AAATTGAAGGTCTTA[C/T]TTTAAAATTGACTTG | 9100 |
| rs559660375 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84746105 | CATGGTTTTTTTTTT[G/T]TGGATTGAGTAAATG | 9100 |
| rs559665565 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84737914 | GCCACCTGGCATTAC[C/T]GGCCCCGCCTCTCCA | 9100 |
| rs559678313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84729776 | GTTGTTTTTTGAGCT[A/G]TGTGAGCCAGTGTTA | 9100 |
| rs559678641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84769844 | GGCTGGTAGGGGTGG[C/T]GGTGTGGGGGCAGGG | 9100 |
| rs559689549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84706597 | CCAGGCTGGAGTGCA[A/G]TGGCGCAATCTCGGC | 9100 |
| rs559705798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84709283 | TTCCCGTGGAAGTGA[C/T]GTGTTTACAGCATGA | 9100 |
| rs559750590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84742004 | TCCAGCTGCAGCAAG[C/T]CCTTTGCAGAGGCAC | 9100 |
| rs559766469 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84705057 | GGCTTGTGTGTACAG[C/T]CTTATCGGTTGTCAT | 9100 |
| rs559780270 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84766905 | ACTTCTAAAACTCAG[C/G]CTCTTCAGATGTTTT | 9100 |
| rs559791500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84768804 | TAAATATAATATAGT[C/T]ATTGTAAATATAATA | 9100 |
| rs559842730 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84770713 | GGAGGCGGAGCTTGC[A/G]GTGAGCCGAGATAGC | 9100 |
| rs559844209 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84720044 | TAAGGTGGAAGTTCT[C/G]TGCTTGATCTTAACA | 9100 |
| rs559860626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84764617 | GGGTGGATCACCTGA[A/G]GTTAGAAGTTCGAGA | 9100 |
| rs559891062 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | USP10 | GRCh38.p7 | 16:84704788 | CTTGAGAACCCAGAA[C/G]CTCTACCAGCACTGC | 9100 |
| rs559894266 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84712878 | TCTGGAGATGATAGG[A/T]CACTTAGCAATGCAG | 9100 |
| rs559933290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84776180 | TCAAGGAAGAAAACT[C/T]ACCACTCTGGCCTGC | 9100 |
| rs559959622 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84716834 | ACCGCATGTCCTGGT[C/T]TAAACTTATCCCAGC | 9100 |
| rs559964201 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84756395 | CTCAGGAGTTCAAGA[A/C]CAGCCTGGCCAACAT | 9100 |
| rs559973732 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | USP10 | GRCh38.p7 | 16:84776929 | GTGATTCTTGTGCCT[C/T]AGCCCCCCGAGTAGC | 9100 |
| rs559990122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84722427 | AGGTTTTCATTTCTT[A/G]TGGGTAAAATGTGGT | 9100 |
| rs560007879 | snp | A/G | 3.31592e-05 | 0.00407167 | intron-variant | USP10 | GRCh38.p7 | 16:84772512 | AAGTAAGACAGGGAC[A/G]GTGTGTCCTGGTGTG | 9100 |
| rs560016892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751417 | AGATATTTTGCACTT[C/T]CTCTTCAAACTCTGA | 9100 |
| rs560037586 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779691 | AAAATGTTAGTCTAC[A/G]TAGATGGGTGATTGT | 9100 |
| rs560070505 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84775799 | CTGTCTCCTGGCTTA[C/G]GCTCCCTGCAGTATC | 9100 |
| rs560124272 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP10 | GRCh38.p7 | 16:84736315 | CCAAAATTAAGAAAT[A/G]TGGGATGTTAAGATG | 9100 |
| rs560169606 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780246 | CTCTTCAGTTGAGTG[C/T]CACTGGGGCGGCTGA | 9100 |
| rs560178699 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84710996 | ACAACAACAAAAATA[G/T]GAATTGTGCCCCTCC | 9100 |
| rs560186286 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84731578 | TTGCACTTGAAAAGT[A/C]GTTTATAGAATTCTA | 9100 |
| rs560194355 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84708692 | AAACAAAACACTTCC[C/T]AACTCAGGTCCCACT | 9100 |
| rs560208051 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84700299 | GCGCCTTCGTCCCCT[C/G]AGCCACCCGGACCCC | 9100 |
| rs560275251 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84744372 | CTTTTTATTACAAAT[A/T]TATTTTAATTTCTAC | 9100 |
| rs560360488 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84725115 | TTCACAAAGTTTTGC[A/G]GCTAACACCGTAGTC | 9100 |
| rs560360738 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84720967 | GGCGCGATCTCAGCT[C/T]ACGGCAACCTCCGCC | 9100 |
| rs560377725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84713176 | TAGATATCTCAGCCA[A/G]TGCCACCATTCACCC | 9100 |
| rs560454308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84761414 | GAACTCAGAAAATGC[A/G]GAAGCTGGTATACCC | 9100 |
| rs560478873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84774427 | GGTAGACTGGTTCCT[A/G]TTTGGAGAAATCATG | 9100 |
| rs560490220 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84763220 | TTATTCCCTACGATA[A/G]CTTACACCATCGAGA | 9100 |
| rs560494019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84725697 | GTGTGAGCCACCGTG[C/T]CCGGCCTGTCTGACG | 9100 |
| rs560508036 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84761148 | AATGGAATGAAGTGC[A/G]CCCTCTGCCCTCAGT | 9100 |
| rs560513847 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699235 | TGAAATCACAGCTAG[A/T]AAAGGGGCCAAAACC | 9100 |
| rs560642154 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84756927 | ACCTTGGAATAAAAG[A/G]GATTTTTAAGTGAAG | 9100 |
| rs560746654 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84756264 | AGGGCTCAGCAGGGG[C/T]TTACTCGCCTTCAGC | 9100 |
| rs560761841 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84762438 | GCTCATGCCTGTAAT[A/C]CCAGCACTTTGGGAA | 9100 |
| rs560770085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84740151 | AATGAAGATGATTTA[A/G]ATTGCACTGACTCTT | 9100 |
| rs560770587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84744401 | ACCTTCTGAAAGCCT[C/T]CCTTAGCTAGAAAGA | 9100 |
| rs560773221 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84761038 | CAGGGGTAGCATAGG[G/T]TCTTAAGCTTTTTAA | 9100 |
| rs560842238 | snp | C/T | | | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719293 | GGAGAAGTAGCTCCC[C/T]TCATCCTCCTGTTTT | 9100 |
| rs560885273 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84723708 | TAACTCGATTCTTGT[A/T]CTTTAAAGAAATCAG | 9100 |
| rs560895101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84746492 | GTCCAGCGTGTTACT[A/G]CTGAATACTGTAGGC | 9100 |
| rs560918474 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84726432 | AACACTGGTTTTCCC[A/G]CTTCGTCTAAACCTT | 9100 |
| rs560944679 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84719088 | TGAGCCACCGCGCCC[A/C/G]GCCAGTTTAGTTGTT | 9100 |
| rs560984942 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84741052 | ATCACTTTAAAGGCC[A/C]TTACTGGCCTCCAGG | 9100 |
| rs561011100 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | USP10 | GRCh38.p7 | 16:84710246 | TGCACTCTAGCCTGG[A/G]CAACAGAGCAGACTC | 9100 |
| rs561038201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84771609 | CGTGGTGGCTCACGC[C/T]TGTAATCTCAGCACT | 9100 |
| rs561078111 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84715155 | GTCTGGTCTCGACCT[C/G]CTGACCTCAAGTGAT | 9100 |
| rs561090201 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84740254 | TTAATTAAATGGTAA[A/G]CGTTGGTTTTAACAT | 9100 |
| rs561094825 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84770725 | TGCAGTGAGCCGAGA[A/T]AGCGCCACTGCAGTC | 9100 |
| rs561108702 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84737453 | CCAGTTACCACAGAC[G/T]AAGTGCATCTGATGT | 9100 |
| rs561126546 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718578 | CTGGCCAACATGGTA[A/G]AACCCTGTCCCTACT | 9100 |
| rs561160625 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84774631 | GCGTGCCACCACGCC[C/T]GGGTAATTTTTTGTA | 9100 |
| rs561172110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84737802 | CTCCCCAGAGTTGTT[A/G]AGGAGCAGGATGTGT | 9100 |
| rs561189790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84714488 | CGTGCACGGCTTTGC[A/G]TTTCTTATATTGTTG | 9100 |
| rs561192786 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84708407 | TGTGAGACAAGATCA[C/T]GCCACTTCACTCCAG | 9100 |
| rs561194662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84754694 | TGATGTAGAAACTAA[A/G]GGTTTCTGTCTGACT | 9100 |
| rs561260355 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84754385 | TGAAAAGGTTTATTC[A/T]GCGTTTAACGACGTC | 9100 |
| rs561289254 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84702401 | GAATAGTAATGCAAA[C/G]AAGTAATGGAATCAT | 9100 |
| rs561311760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84750645 | TCCTCATATACTAGA[C/T]GAAATTGTATCAGAT | 9100 |
| rs561341925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84709920 | GGAGAGGAGAGAGAA[A/G]GAATTTGGTAATCCA | 9100 |
| rs561411637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84733119 | AGGTAAATGGAACAA[C/T]TGGCAGTATTTGTGA | 9100 |
| rs561448347 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84756888 | AATAGACTTTAAGCC[A/T]GTGGGGAAAAGTAAG | 9100 |
| rs561465485 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84706024 | ACTGCCCCCAGCATC[C/G]CTACTCATTCTTTGA | 9100 |
| rs561506092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84735188 | GGTGTGTGCTGCCAG[A/G]CCCGGGTGGTGTGTG | 9100 |
| rs561527947 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84706452 | TAATAATTTCCCTTA[A/C]GTGGCTGCAAAGACT | 9100 |
| rs561543695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84775834 | TTTCTGCCACATCAT[C/T]TTCCCTTTCCTTTCT | 9100 |
| rs561546828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84774930 | ATCACAGCCTCGGCC[A/G]TTGCTCCTGTTTCTT | 9100 |
| rs561556244 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84732700 | TGATTCGCCCATGTC[A/T]GCCTCCCAGAGTGCT | 9100 |
| rs561574474 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84735697 | TCACAGAAGACGTGA[A/C]TGTGTCTCATGAAAA | 9100 |
| rs561614354 | snp | A/C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779807 | CCTTCAGTCTGCTCT[A/C/G]TTTAATTCTGCTGTC | 9100 |
| rs561619101 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84727807 | TGTATTTCCTAAGAA[C/T]AGGCATATTCTCTTA | 9100 |
| rs561677488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84776056 | CACTGCCATTTATTG[A/G]CCTTCACACATGTAT | 9100 |
| rs561717003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751458 | CAGTGGTCATGCGGC[A/G]TGATCTAAGTTAAAA | 9100 |
| rs561720470 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84750306 | CTAGCTACTGAGGAG[A/G]CTGTGTCAGGAGAAT | 9100 |
| rs561728461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84716883 | CCTTTCACTCTGAGA[C/T]ATGCCTCTAATTTGG | 9100 |
| rs561762511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84730323 | TCTTCTTTTAATAGT[A/G]TTTTGAAGATCTCTC | 9100 |
| rs561772740 | snp | A/C | 1.65737e-05 | 0.00287864 | synonymous-codon, nc-transcript-variant, intron-variant | USP10 | GRCh38.p7 | 16:84759452 | AAGGCCTTGTACGTC[A/C]ACACCCATGATAGAC | 9100 |
| rs561824704 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84736915 | TGCCTCAGCCTCCCG[A/C]GTAGCTGGGACTACA | 9100 |
| rs561826097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84725712 | CCCGGCCTGTCTGAC[A/G]ACATTTTCAAACCCG | 9100 |
| rs561840246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84763452 | ATCCATATATACATA[C/T]ATACGCATACATTTT | 9100 |
| rs561870402 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779238 | CCTTGGGGTTCGTGC[A/G]CAACACAGCTTCTGT | 9100 |
| rs561897309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84759678 | TGTTCTTTAGATTCA[A/G]TAGAAAATATTTTAG | 9100 |
| rs561961794 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84720101 | GCTAATGTAAGTACT[G/T]CTTATTAGACAGTCC | 9100 |
| rs561962232 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84725200 | CCGCCTCCCGCTCCC[C/G]CATTCTCCTCTCCTC | 9100 |
| rs561966745 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84734345 | GTAAATGGACTCTCA[C/T]TGTTTTAATTTACAT | 9100 |
| rs561991327 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84775389 | GTTTTACCTGAAACT[C/T]TGCGTAGATGACGGA | 9100 |
| rs562024911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84720512 | TGAGTAATGATGGGA[C/T]AGAGGCTTCAGAGTG | 9100 |
| rs562027556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84738828 | TGTGCTGAGATCTCA[C/T]TGGAGAACTCAGCTG | 9100 |
| rs562042752 | snp | C/G/T | 0.000103993 | 0.00721023 | intron-variant | USP10 | GRCh38.p7 | 16:84760159 | GAAAACCTGTGTCCT[C/G/T]TTTCCATTGCAGCTC | 9100 |
| rs562090616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84756419 | CCAACATGGTGAAAT[C/T]CTGTCTCTCCTAAAA | 9100 |
| rs562113559 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84761993 | GGGCAAGTAAACTTT[A/G]CAGTTTACCTAGATG | 9100 |
| rs562138789 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84746816 | AACTTTTTTACGTTT[C/T]ATTTTACTTTTAAAT | 9100 |
| rs562139642 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84700408 | TCCCTGGGGCTGGAC[A/C]GCGGGGCGAGCCCGG | 9100 |
| rs562141607 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84705512 | CTGGGATTATAGGCG[C/T]GAGCCACCACACCCA | 9100 |
| rs562149739 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84760400 | AGATGTAGGTTTATA[A/C]GAGTCCATTGCTTGG | 9100 |
| rs562170391 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84770227 | TGTTACCAGATGAGG[A/C]CAGGACCACTTTCAA | 9100 |
| rs562179470 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84763620 | CATCTTCAAATTTCG[C/G]CAGTTGTCCCAGGGA | 9100 |
| rs562201334 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84700743 | TGAGTGACATCCCTT[G/T]CACGAATCCATCCCA | 9100 |
| rs562213553 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84776819 | CCTCATCCCCTAACC[C/T]ATTATTTTTTTGAGA | 9100 |
| rs562293311 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698648 | TCACCCAGGCTGGAG[C/T]GCAGTGGCACGATCT | 9100 |
| rs562351180 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718299 | TACTCTGTGACCCAA[C/G]ATAGAGTGCAGTGGT | 9100 |
| rs562373431 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84756454 | AAAAATTAGCCGGGC[A/G]TGGTGGTGCACGTCT | 9100 |
| rs562396594 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84752523 | TATTGGACTTTAGGC[G/T]AGGAATAACATTGTA | 9100 |
| rs562413647 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84747969 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 9100 |
| rs562423198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718620 | AATTAGCCCAGACAT[C/T]GTGGCACATGCCTGT | 9100 |
| rs562430142 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84748070 | GAGACAGGAGAATGG[C/T]GTGAACCTGGGAGGC | 9100 |
| rs562486553 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84714641 | CATACTAAAAATGGT[A/C]ATGTTTGGCAGGTTT | 9100 |
| rs562549328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84722861 | GCGTCCGGCTCAGTC[A/G]TCTTAATTTTATAGT | 9100 |
| rs562555049 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84773627 | TGCCGGGTTTAGTGT[C/G]CGTTGCTCCTCTCAC | 9100 |
| rs562588336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84727279 | TTGTAAATCCTGTGA[A/G]GTCAGACACAGCGTT | 9100 |
| rs562593483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84748649 | CTCCACAAAGGAAAA[C/T]CTCCCATCTTAGGGA | 9100 |
| rs562610772 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84726871 | ATTTCCTATGCAACC[A/G]CAGGACGCGGGAAAG | 9100 |
| rs562617273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84777787 | TGTTTGGTCTTGTTT[C/T]AGTGCTGAAATTCCC | 9100 |
| rs562617420 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84776733 | TGTGAGCACACACAC[C/T]CCTCCCCGACTCTGC | 9100 |
| rs562649231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84722447 | TAAAATGTGGTAAGC[A/G]TATATTCTATTCTGT | 9100 |
| rs562691332 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84774871 | CAGCTTTTTTCTTTT[C/G]CATTTTGTAGAGCAC | 9100 |
| rs562734330 | snp | A/G/T | 8.28087e-05 | 0.00643415 | synonymous-codon, nc-transcript-variant, intron-variant | USP10 | GRCh38.p7 | 16:84758756 | CCATAAACCAGTGTC[A/G/T]TTGCAACCCCGTGGG | 9100 |
| rs562853008 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84743980 | ATTGAAGGTTACCAG[C/T]GGAGGAGACCAAGAG | 9100 |
| rs562886542 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84721308 | GTGTACTGAAGAATT[A/C]TTCTTCCGTAGATGA | 9100 |
| rs562922760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84749814 | GATTACTCTTAAACT[A/G]TCCACTTTAACGGGT | 9100 |
| rs562949260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84721837 | CGAGTAGCTGGGACT[A/G]CAGGCACACGCCGCC | 9100 |
| rs562969124 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84744228 | GTTTTAAGTCCCTAA[C/G]TTAGTTGTCATGATC | 9100 |
| rs562986171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84749387 | TTGCATTAGTATCTA[A/G]CTGTTTCTACTGAGA | 9100 |
| rs562988007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84753604 | GGCAGAGCCAGGGCG[C/T]GAACCCCCGTCTTCC | 9100 |
| rs562990476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84746584 | GTACAGATATGGTAT[A/G]AAGGATGAAAAGTGC | 9100 |
| rs563013980 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717792 | TTGATTCATTGAGGT[A/C]CTAGTCTCTGGTCCT | 9100 |
| rs563040532 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84740864 | CTGGTCTGTTACTTT[A/T]TTGGGTCTCCATCAC | 9100 |
| rs563051620 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84753148 | ATTTTTTTATTTTTT[A/T]TTTTTTATTTTTCAT | 9100 |
| rs563072178 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84744475 | ATTTTATAGTTGTTT[C/G]ATTTTCCGCAAATTG | 9100 |
| rs563102070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84713510 | TCTCGTCCTCCCCCA[A/G]TGTAAGCTCCTTGAG | 9100 |
| rs563116633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84754741 | CAAATAAATGCTGGG[A/G]AAAAAGTCGGTTTAT | 9100 |
| rs563173011 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84736377 | TCCTGCCAGCGGAGG[C/G]CTGCTTTGTCTTTTA | 9100 |
| rs563216254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84774979 | TTTTGTGTCCTATTA[C/T]GTCACATGGCTCATT | 9100 |
| rs563268550 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84722721 | GACTCCCCCACGCCC[A/C]GCTAATTTTTGTATT | 9100 |
| rs563278563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719548 | CGAGGACTGTTGTCT[C/T]AGGCCTTTGTCCAAT | 9100 |
| rs563295482 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84773611 | ACGGGCTTGGCTGCT[C/G]TGCCGGGTTTAGTGT | 9100 |
| rs563304516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84724659 | GCTTCTGCCATTTGT[A/G]ACACTTAGTTCAGCT | 9100 |
| rs563309263 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84763789 | ATCCAGTGACGTTGC[A/C]CCTGTTGCGATTGGT | 9100 |
| rs563310190 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84742504 | CTGCCTTGTAGTCCA[G/T]TCCTCTCTACTGCAT | 9100 |
| rs563332272 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84711692 | CTTCCACCTATAACT[A/G]GAGTTTTAGGCGTGA | 9100 |
| rs563339168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84754430 | TTTCAAAGACTGTCA[A/G]AGGCTTGAAGGAAAG | 9100 |
| rs563341831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84720004 | CTAAGTAACTTTGCT[C/T]TCCATTAACAACAAA | 9100 |
| rs563348301 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84715009 | TCTCGGCTCACTGCA[A/C]CCTCTGCCTCTTGTG | 9100 |
| rs563368867 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84768426 | GAAAGAACACAAAAT[G/T]AGGAATGAGGGGAAA | 9100 |
| rs563378683 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84724244 | ACTGGAAAGTTGGTA[A/G]AAGTGGGTTTCTGTT | 9100 |
| rs563379269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84737511 | GCTGTGTGCCTGTGG[A/G]ATAAAACACACACAT | 9100 |
| rs563391326 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84707561 | GTTTCATAATATGGT[C/G]TGTTGTATCTAGTCA | 9100 |
| rs563406432 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84704093 | GCTCAGAATATAACA[A/T]TCAAGTAATTGAGAA | 9100 |
| rs563427095 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84711422 | GAGAACTGGAACTTT[A/G]TAATTCATCCTGAAG | 9100 |
| rs563440139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84762506 | GACCAGCCTGGCCGA[C/T]ATGGTGAAACCCCGT | 9100 |
| rs563488569 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84745831 | GTTCTCTAAAAGTAA[A/G]ATAATATAGAAACAA | 9100 |
| rs563492433 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84752107 | AAATTTCAGTTCAGC[C/T]TTTTCATGTGAGTTA | 9100 |
| rs563500633 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84766521 | TAGGATTGTGAGGAC[A/G]CCCCCTCGGGATGGG | 9100 |
| rs563515561 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84702244 | TGTATTTTTATTAAA[A/G]ACGGGTTTCACCATG | 9100 |
| rs563530800 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84772127 | CGCGAACTTAGCTCA[C/T]TGCAACGTCTACCTC | 9100 |
| rs563531798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84747086 | CTTGTGGGACCATCA[C/T]ACGTGCGGCTCATTG | 9100 |
| rs563532631 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84742862 | TTCTGTTCACGTTAC[A/C]TCACATTCTAGAATG | 9100 |
| rs563542333 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84761599 | GAAATGCTGCCAACC[A/T]GGGAAGGTCATTACA | 9100 |
| rs563564423 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84733590 | TTTTTTTAAATAAAG[A/T]ATTCCAATGTAGAGA | 9100 |
| rs563567823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741614 | CTGCCTGCCCTTTTC[A/G]GTGACTGCTTCTTGG | 9100 |
| rs563569007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84734373 | CATCTCCCAGATTAC[A/G]AACAGCTGGGTACTA | 9100 |
| rs563656260 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84750659 | ACGAAATTGTATCAG[A/G]TGCTTTCACATCACA | 9100 |
| rs563671385 | snp | C/T | 0.000233727 | 0.0108078 | intron-variant | USP10 | GRCh38.p7 | 16:84759498 | TGGTGAAAGATGTGT[C/T]AAGTGGTGGGGTTTT | 9100 |
| rs563692433 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84772133 | CTTAGCTCACTGCAA[C/G]GTCTACCTCCTGGGT | 9100 |
| rs563734170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84713064 | AGCAGCCAGCCTTTC[C/T]AGTACAGGGCCCAAT | 9100 |
| rs563755445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84775393 | TACCTGAAACTCTGC[A/G]TAGATGACGGATTAT | 9100 |
| rs563762825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84776592 | AGTGTGGCACCCAGG[C/T]CCCAGTGGGTGGCCA | 9100 |
| rs563812113 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84728719 | CCATTTTCCCTTTTT[G/T]TAGTTTTATCAGCAT | 9100 |
| rs563833599 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84735870 | GCTAATTAACATAAT[C/T]GGATGGAGTTGTTTT | 9100 |
| rs563872986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84724106 | ATACAATAGCAATTT[C/T]ACACAGGAAGTTATT | 9100 |
| rs563886759 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84775868 | TTCCCTTTTATCCTT[C/G]TTTCTCTTTTATAGC | 9100 |
| rs563900418 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84706829 | ACAGGCGTGAGCCAC[C/T]GCGCCGGGCCAAGAC | 9100 |
| rs563980053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84760083 | ACATTCAGCCAGGTG[A/G]GAGGTGGGGGAGTTT | 9100 |
| rs564041782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84743809 | TTAACTGGGAAGGAA[A/G]TATTGAAGGCTTCCC | 9100 |
| rs564042397 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84769900 | TGTTGTTAGACGGTA[A/G]TGAAGAAAGAATGGT | 9100 |
| rs564071541 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84773537 | CGCCCTATACCTTCC[C/G]GTGAAGACTCAGACA | 9100 |
| rs564097561 | in-del | -/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698145 | CCCAATTTTTTGTTA[-/T]AAAAATTTTCAAACA | 9100 |
| rs564106353 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84705018 | GGTGGCTGCTCCTAA[C/G]AGTCCTCAGTCTCCT | 9100 |
| rs564142553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84740118 | TTTGAAAGCATTTCT[A/G]TTGTGTTTTTTTCGT | 9100 |
| rs564167599 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84755528 | TCTGGGGACCTGTGC[C/G]TATGTTTGTGTGATT | 9100 |
| rs564171500 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84759251 | CATATCTAAGTAGTT[C/G]AACGTCCTTAGCTTC | 9100 |
| rs564203952 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779114 | GTGTGCGCCCAGTGC[C/T]CGCTTCGTAGGACAC | 9100 |
| rs564226063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84704720 | TTTTCTGAACTGGCT[A/G]TTTTCTGGCTATTTG | 9100 |
| rs564226855 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84759734 | ATAGACCAAAAATGC[A/G]TATAGAAGAGACTTG | 9100 |
| rs564253856 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84751521 | TGTGGACTGAGAGTT[C/T]AGTCCACATCTGATT | 9100 |
| rs564315166 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84700056 | AGCAGCGTGAGCAGC[C/T]GGAGGATCGCGGAGT | 9100 |
| rs564400632 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84701820 | CAAAAGTTGGCGGAA[C/G]GTAAATGTTAGCAAC | 9100 |
| rs564410812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84716955 | ATAGGGACAGTCACT[A/G]TGATAGCAGTGTGCT | 9100 |
| rs564422634 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84777298 | CATTTTAGAATGGAG[A/T]TGTCTTGTGGGAAAG | 9100 |
| rs564433004 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84756453 | CAAAAATTAGCCGGG[C/T]GTGGTGGTGCACGTC | 9100 |
| rs564434838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84734778 | CAGATTTTGTTTTCA[C/T]GCTTCAGTGTGTAAT | 9100 |
| rs564436522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84729371 | CCTAGCTTGTGATAT[C/T]GATGACTTGTCTTTT | 9100 |
| rs564463467 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84747758 | TTTTAGTAGAAATGG[A/G]GTTTCACCATGCTGC | 9100 |
| rs564476132 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84761307 | CGTGCACAGAGATAA[C/T]GCTATGAACAAAAGC | 9100 |
| rs564487937 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84752601 | GATATTAGAAATTTG[G/T]AAGTGGTATTAGTTC | 9100 |
| rs564497112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84729717 | CACTTTTAAAAGCTC[A/G]TGCATTTAAGGATTA | 9100 |
| rs564550229 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84756833 | AATGATAGACTGTTG[G/T]GATGATATGGTTTAA | 9100 |
| rs564558114 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84730124 | CCTCCACTCCTGTCT[A/G]CGTCCACTCAGCGTC | 9100 |
| rs564580372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84760948 | GTTGAGAAAATGCCA[C/T]TTAAGTCAAGTTTAC | 9100 |
| rs564582162 | snp | A/G | 0.000315209 | 0.0125501 | intron-variant | USP10 | GRCh38.p7 | 16:84732478 | TTGAGATGGAGTCTG[A/G]CTCTGTCGCCCCGGC | 9100 |
| rs564607937 | in-del | -/A | 0.36285 | 0.223081 | intron-variant | USP10 | GRCh38.p7 | 16:84762691 | TGAGACTTTGTCTCA[-/A]AAAAAAAAAAAAAGT | 9100 |
| rs564642437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84760422 | ATTGCTTGGATGATA[C/T]GGTGCACCAAGCACT | 9100 |
| rs564642715 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84764826 | CAGAGTGAGACTCTG[A/T]CTCAAGAAAAAAAAA | 9100 |
| rs564647471 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84725591 | TGTGTTTTTAGTAGA[C/G]ACAGGGTTTCACCAT | 9100 |
| rs564708002 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84701342 | TTAACGTTTTGTTCC[C/G]TTATTCATTTACTTT | 9100 |
| rs564810768 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84715113 | TTTATATTTTTTAGT[A/G]GAGATGGGGTTTCAC | 9100 |
| rs564879843 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84723655 | CCTACTCTATGCCAA[C/G]TCTACTGCATTAACT | 9100 |
| rs564882747 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84710497 | GCAGGTAGCCCTTCA[A/G]TGTCCTCAGTGGTAA | 9100 |
| rs564960435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84775083 | CTTGCTGGGGAGAAT[A/G]TTGTTAGCCATTTTC | 9100 |
| rs564981018 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84744538 | TGATTAGGAAGAGAA[C/G]TTAAGGTTTTTATTT | 9100 |
| rs564991766 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84765572 | TAGTATAATGTTCCC[C/T]AGGTTCATTCCTGTT | 9100 |
| rs565039386 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84713071 | AGCCTTTCCAGTACA[C/G]GGCCCAATTATGTGT | 9100 |
| rs565042096 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718680 | AGAATTGCTTGAACC[C/T]AGGAGTCGGAGGTTG | 9100 |
| rs565051287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84752915 | CAATAAGTATTTAAT[C/T]TTCATTTCTTACAAT | 9100 |
| rs565053278 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84756645 | TTTGAGTCTTAAGGT[C/T]AGGTTTAAAAAAAAA | 9100 |
| rs565086133 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84774946 | TTGCTCCTGTTTCTT[C/T]AGTGAGCTGGCTGCA | 9100 |
| rs565091834 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84771515 | AAACAAACAAACAAA[A/C]AAACCCACCTAATCC | 9100 |
| rs565109557 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84705063 | TGTGTACAGCCTTAT[C/T]GGTTGTCATTCTTCG | 9100 |
| rs565117617 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84745943 | ATTTCCATTTCTTGC[C/G]TTTTGTTCAAGTAAT | 9100 |
| rs565144582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84777844 | GGTTCCTTTTCTTTT[A/G]TGCCACTGATGGTGG | 9100 |
| rs565148978 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84727987 | GAAATGTATTTAGTT[A/G]TCATGTCTCTAGCTT | 9100 |
| rs565161713 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84773975 | TAAATGGGGGCTGGG[C/T]GCAGTGGCTCACACC | 9100 |
| rs565162139 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84728376 | TTTTTTTTTCTCGCT[A/G]TTGCCCAGGCTGGAG | 9100 |
| rs565181512 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84721492 | AAGTATAATTTAATA[A/C]AATAAATGTACCCAT | 9100 |
| rs565187434 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84726536 | CCAGCTTAGCCAACA[A/G]GCTATGCTTCAGGGA | 9100 |
| rs565238825 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84775936 | TTGTTGCTGTTTGCC[A/G]CACTTTTGTTTGCTT | 9100 |
| rs565242966 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84751441 | ACTCTGAAGTACACA[C/G]GCAGTGGTCATGCGG | 9100 |
| rs565243728 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84757740 | CAGTGTGGATTGGCT[A/G]CAGATTATGGAGTTG | 9100 |
| rs565250828 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84768858 | ACTCTTTGATTTGAT[C/T]TGGAAAAGGTAAGAT | 9100 |
| rs565254091 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84700825 | GCCCTTTACAATAAT[A/C]CCGTGGTGGAAAGAA | 9100 |
| rs565255309 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84750196 | GTGGATCCCTTGAGG[C/G]CAGGAGTTCAAGACC | 9100 |
| rs565291467 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717874 | TTCATTCAGTTGCTA[A/T]TCTTGCCAAATGCAG | 9100 |
| rs565318722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84754336 | CATTAAGAAAAATCT[A/G]GGTTGTTCGTGTCTC | 9100 |
| rs565369918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741205 | CTAACCAAACGTTTT[A/G]TCTCCAGTAACATCA | 9100 |
| rs565409584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84702724 | ACAGGCCAGCGCGGT[A/G]GCTCGTGCCTGTAAT | 9100 |
| rs565446164 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84740987 | TTTAATTATTGATTG[C/T]AGGCTGCCCTTGCAC | 9100 |
| rs565456468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84705992 | CTCCCAAAGTGCTGG[A/G]ATTACAGGCATGAGC | 9100 |
| rs565506979 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84736991 | GGCGGGGTTTCACCG[C/G]GTTAGCCAGGATGGT | 9100 |
| rs565520509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84753779 | ACAACTTTAATCTCC[A/G]GATGTTTAATTGATC | 9100 |
| rs565528618 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84705523 | GGCGTGAGCCACCAC[A/G]CCCAGCCACTCCTGT | 9100 |
| rs565574706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84732326 | GCTTACCATTTTTAT[A/G]CCCAGTACTGATCAT | 9100 |
| rs565581543 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84738552 | GCCAGCATCAATGCT[A/G/T]GTGTGTGGAATGGTC | 9100 |
| rs565583038 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84769209 | AATAAGGTGCCCCAA[C/T]GTAGAAGACCTGTCA | 9100 |
| rs565643815 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84733958 | TATGCTAAGAAATTT[G/T]TCCTTGTTCTTTGAT | 9100 |
| rs565647848 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84750442 | AACTTAATAGCTTGT[A/G]TTTGAAAGTAGTTGC | 9100 |
| rs565691776 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84711510 | GAATTCCTGCTCTCT[G/T]TTGCTGTTGTTGCTC | 9100 |
| rs565700119 | in-del | -/TTG | | | intron-variant | USP10 | GRCh38.p7 | 16:84748769 | AGTTTGATAAATAGT[-/TTG]TTATGTTCTGTATAT | 9100 |
| rs565709130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84755642 | TCCTGTCTTTAAAAT[A/G]ATAATTATGATTGGG | 9100 |
| rs565710539 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84754508 | TGTTCTGCTGTTGCA[G/T]AGGTTGTGCTCGTTC | 9100 |
| rs565719224 | in-del | -/TTTTTTTTT | 0.48546 | 0.0840147 | intron-variant | USP10 | GRCh38.p7 | 16:84711720 | TGAGGAAGGGCTAGC[-/TTTTTTTTT]TTTTTTTTTTTTTGT | 9100 |
| rs565762621 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84775009 | TTCCTTCATGAGTCA[A/G]TTTTTGTGCAACTGA | 9100 |
| rs565772293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84755254 | ACCTCTGGCATCTTC[A/G]CCCTAACTCTGCCCT | 9100 |
| rs565832411 | in-del | -/CTAA | | | intron-variant | USP10 | GRCh38.p7 | 16:84749384 | GACTTGCATTAGTAT[-/CTAA]CTGTTTCTACTGAGA | 9100 |
| rs565833612 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84759571 | TGATTTCCTGCAAAT[G/T]AGTCCTATAATTCTG | 9100 |
| rs565837219 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84734402 | TATTTCATTCTCTTC[A/C]CGTCTGCTGGCAATA | 9100 |
| rs565857733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84703325 | ATTGATGTCATTTAT[A/G]GTGAAATCTCCACAA | 9100 |
| rs565901941 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84700755 | CTTGCACGAATCCAT[A/C]CCAGCCAGGCTGACA | 9100 |
| rs565908341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84729509 | AGGAAAAAGATACAT[A/G]TAGTTTATCTGCCAT | 9100 |
| rs565910900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751292 | GCCACATTTCTCAGA[A/G]CATATCCCCATCATT | 9100 |
| rs565920945 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84768701 | TTCATGATACCGTAG[C/G]GTACAACTGTCATTA | 9100 |
| rs565925444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84701604 | CCTTGTGATTTTGAC[A/G]TGAAGAAAGCATCTT | 9100 |
| rs565936996 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84723860 | ATTCCCCAGAATGAC[A/G]TTGAGCCCCCTTGCA | 9100 |
| rs565986793 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84735707 | CGTGACTGTGTCTCA[C/T]GAAAATGAGCTCAAG | 9100 |
| rs565994344 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84750462 | AAAGTAGTTGCAAAA[C/T]GCGACACCCTTGTTA | 9100 |
| rs566047563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84746692 | GAGTGAATGTGAAGG[C/T]CCAGGACAGTACTGA | 9100 |
| rs566082211 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84763893 | TTGGTTGCCGTGGAT[A/C]CAGTGACATTGTGCC | 9100 |
| rs566094912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84733317 | TGTTTAATTGAGAAA[A/G]GATCTTGGGGGTTAT | 9100 |
| rs566115552 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84702171 | AAGCGATTCTCCTGC[C/G]TCAGCCTCCCAAGTA | 9100 |
| rs566139751 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | USP10 | GRCh38.p7 | 16:84706346 | AAACAATTTTTTTAT[A/G]CTTCATTTTTTAGAG | 9100 |
| rs566156050 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84723412 | ATATTTGAGAATGAA[A/G]GATGTACTCCTAGCT | 9100 |
| rs566156570 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84766857 | TCAGCCATTGTTAAG[C/T]ATGATTCTTTATTCA | 9100 |
| rs566161502 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84725873 | TCTTTTCATGTTTCC[C/G]CAAATTGAGCTTATT | 9100 |
| rs566163935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84763201 | TTTTCCTTTCAAATA[A/G]CATTTATTCCCTACG | 9100 |
| rs566166041 | snp | C/G/T | 0.00598604 | 0.0543924 | intron-variant | USP10 | GRCh38.p7 | 16:84732479 | TGAGATGGAGTCTGG[C/G/T]TCTGTCGCCCCGGCT | 9100 |
| rs566171396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84762189 | TAACGCTCTAAATCA[A/G]TGGAGTTTTTCCACA | 9100 |
| rs566222657 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84721050 | AGGTGCCCGCCACCA[C/T]GCCTGACTAATTTTT | 9100 |
| rs566223655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84763526 | ATCTCAGGTGCTAAA[A/G]CATCTCCTGCGTAAC | 9100 |
| rs566225419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84767165 | AGCTCTTCACCGCAT[C/T]TGTTCTGGAAAGCCT | 9100 |
| rs566225590 | snp | A/G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84748947 | TTTTAATCCTATTTG[A/G/T]TTAGGTCAGTTATGA | 9100 |
| rs566243116 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84747081 | AGAATCTTGTGGGAC[A/C]ATCATACGTGCGGCT | 9100 |
| rs566254884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84715538 | AGTGAGTCCACCTGG[A/G]TGACCTTACTACTTT | 9100 |
| rs566282328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84721451 | ATAGATTGTGCATAA[C/T]AATTTTTAAAAAGTC | 9100 |
| rs566347635 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84772843 | TAATAGACCTTAATA[C/G]TAAAATTCTCATGAA | 9100 |
| rs566385596 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84764862 | AAGATACAGGAGAAT[A/G]TCATCATGACTTAGG | 9100 |
| rs566401862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84715770 | TTGGTTTAATTCAGC[C/T]GTTTAGTTACAGTTT | 9100 |
| rs566404672 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780264 | CTGGGGCGGCTGAGC[A/G]GTGCCTCCAGACGCC | 9100 |
| rs566405242 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699790 | CTTCCGGATCCACAG[C/T]CAGGCCTCGGCGGGC | 9100 |
| rs566408946 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84775883 | CTTTCTCTTTTATAG[C/T]GTCATCTTTTATGCC | 9100 |
| rs566436019 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84763917 | TTGTGCCTGTTGCGA[C/T]TGGCCGTGGATCCAG | 9100 |
| rs566443507 | snp | C/G | 2.86004e-05 | 0.00378145 | intron-variant | USP10 | GRCh38.p7 | 16:84744610 | GAACTGGGTTCTTAA[C/G]TAATAGTTTTCTTTC | 9100 |
| rs566443574 | snp | A/G | 6.62647e-05 | 0.00575569 | synonymous-codon, intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84740317 | TGTGCAGCTTCCTCC[A/G]TACAGTGGAACAGTT | 9100 |
| rs566461343 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699360 | CCCGTGCACACGCAC[A/G]CACGTGTGCAACACG | 9100 |
| rs566626555 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84709799 | GGACAAGGGCATGTG[G/T]AGGAGACTGTGCAGA | 9100 |
| rs566706025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84720240 | TCTGCCGTGGCGATG[C/T]GCGTTCCTTCCTGGC | 9100 |
| rs566708263 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84775575 | CTGTGGAGTTTCCAC[A/G]ACACCTGGTCACCCA | 9100 |
| rs566712494 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84700265 | TAGGCCGGAGCCACC[C/T]GCCGCCTCCGCGCCC | 9100 |
| rs566735254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84708336 | GCACCTTTAATCCCA[A/G]CTGCTCCGAAGGCTG | 9100 |
| rs566737618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84713351 | GTCTCTGTGCCTGGG[C/T]CATCTTCTTACACCC | 9100 |
| rs566767240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84716208 | AGATATGCCAGTTCC[C/T]CCTGGACTCCTCAGA | 9100 |
| rs566802577 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84749100 | ATAGTAGAGCAATAG[A/T]GTCACATTGAATAAC | 9100 |
| rs566823980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84725374 | GCATTAGTCTGATGA[C/T]ATTTTCTTTTTCTTT | 9100 |
| rs566828276 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84769986 | TGGTGGCTCACGCCC[G/T]TAGTCCCAGCACTTT | 9100 |
| rs566831195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84777084 | TAGAATTACCTGTAG[A/G]GTGAGCAAAGGAACA | 9100 |
| rs566847147 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84727258 | GGCATTTCCCTCTTC[A/C]CTAGGTTGTAAATCC | 9100 |
| rs566870356 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84720755 | CCCAGCTAATTTTTT[G/T]TATTTTTTAATAGAG | 9100 |
| rs566889544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84769740 | AGGTGGTCAGCCTTT[C/T]CATGGGCTGCCTAGG | 9100 |
| rs566933021 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84716666 | GGAGCTGCCTGCACG[A/G]AGGCTGATCAGCAGA | 9100 |
| rs566969073 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84748730 | GTTTTAGAACATTCT[A/C]CTTAGTCATATGACT | 9100 |
| rs566985276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84743094 | CATCAGGGAATAGGG[A/G]ATGTATGGAACCAAA | 9100 |
| rs566991655 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84735014 | GTTTTATTTTATTTT[A/T]TTATTTCTATTTTTT | 9100 |
| rs566994764 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84714300 | AATGACACTTGTTTA[A/G]TAAAATGTTTTTCCC | 9100 |
| rs566995048 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84776793 | GGTTGCTCTCCCCTG[C/G]CCTCCTGAATCCTCA | 9100 |
| rs567025146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84704020 | AGGAGAAAAGGATTA[C/T]GAAGCTTAATGATTG | 9100 |
| rs567109208 | snp | A/C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84755191 | CTTTCATTTCCTTCC[A/C/G]GTATCAGTGCTAAAC | 9100 |
| rs567131001 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84706207 | ATTCTGCAAGTATCA[G/T]TCTTTTTACTTTTGA | 9100 |
| rs567155662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84735322 | AGTTGCTACAGGTTT[C/T]CTCAAGTGTGTACAC | 9100 |
| rs567173665 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84756237 | TGTGCCTTCCTTACC[C/T]GGTGCCTAGGCAGGG | 9100 |
| rs567173766 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84760546 | CTGAGGTCAGGTAGC[A/T]AATGTACATGGCAGA | 9100 |
| rs567195865 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84706623 | TCGGCTCACTGCAAG[C/T]TCCGCCTCCCGGGTT | 9100 |
| rs567207069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718449 | TGTCATATTACTTCT[A/G]ATTTAGTTGCATTAT | 9100 |
| rs567227924 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84714847 | CATGAATTTTTTTAA[A/C]TTTTAAAAGTAATAT | 9100 |
| rs567255911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84777550 | GCTGTGTCCCTGGCT[C/T]TCCGAAGTACGGGCC | 9100 |
| rs567259031 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84702211 | ACAGGCGCCCACCAC[A/C]ATGCCTGGCTAATTT | 9100 |
| rs567279642 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84728214 | TGTGATAAACTTTTT[G/T]GTGTCACAAACATGC | 9100 |
| rs567287892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718739 | CCAGGTTGGGCAACA[A/G]AGCAAGACTGTCTGA | 9100 |
| rs567297881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84740583 | GTGCCAGCCATGTAA[A/G]ATTTAGTTTAGGAAA | 9100 |
| rs567343370 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84715786 | GTTTAGTTACAGTTT[C/T]GAGGACGTGGCTTCT | 9100 |
| rs567371705 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84770680 | AGGAGGCTGAGGCAG[A/G]AGAATGGCGTGAACC | 9100 |
| rs567393914 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84767779 | AGAATTATTATTATT[A/T]TTTTTAATTTATTTT | 9100 |
| rs567414853 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84766648 | ATACTCAAAGATCCC[A/C]AATTTGTCTAAGAGT | 9100 |
| rs567441091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84737632 | TGAAGGTGGCAGTGT[C/T]ATCTGGGAGTTTGCT | 9100 |
| rs567444898 | snp | A/G/T | 0 | 0 | intron-variant | USP10 | GRCh38.p7 | 16:84741745 | GGCCTGCTTTTCTCT[A/G/T]CAGCCTTTCTGGGTA | 9100 |
| rs567464191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84710959 | GACAAAGTGTTACAT[C/T]TCCAGTCTAGGTTAG | 9100 |
| rs567471474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84766250 | AAGCCAGTTGAGCAG[C/T]CATGTGACCTTGAAC | 9100 |
| rs567488847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84732833 | CAGTTTAACCACTTC[A/G]TTTTCCAGAAAATCA | 9100 |
| rs567522147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84701668 | TCAATCACAATTCAA[A/G]GTTGATTGAAATGTT | 9100 |
| rs567531168 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84704352 | CTGTTACTTTTCTAT[G/T]TACTGCCACACATGC | 9100 |
| rs567544517 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84765174 | GTGTATATTTAAAGT[A/G]TACACAGATGTTATG | 9100 |
| rs567613968 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84751068 | AGTCAACAACAGACC[A/G]CATGTACGACAGTGG | 9100 |
| rs567659467 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84774553 | TCGGCTCGCTGCAAC[C/G]TCTGCCTCCCGGGTT | 9100 |
| rs567674104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84709555 | CTGCCCAGTGAAGAA[C/T]AGACTCACGGGGTCG | 9100 |
| rs567692355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84736634 | ATGCTCACCATTCTT[C/T]AGTTTCCAGAATCTC | 9100 |
| rs567742051 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84762184 | ACAGCTAACGCTCTA[A/C]ATCAGTGGAGTTTTT | 9100 |
| rs567751940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84731935 | TATATTCTTCACTGA[A/G]AAGTGACAGTATTTC | 9100 |
| rs567785229 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84700527 | CAGCTCAGGTTGCTG[C/T]CTCTGCCTGGAGCGA | 9100 |
| rs567813547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84734866 | CCCCTGTGGCCCTGG[C/T]AGGTGCCTCCTCACC | 9100 |
| rs567825807 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84737532 | ACACACACATTTCCA[C/T]AGTGCCACAACCCAT | 9100 |
| rs567827254 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84726900 | AGGAGCGTTTGTTAC[C/T]GCTTTCTGATACCTC | 9100 |
| rs567905222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84777867 | GATGGTGGGCGCAGC[C/T]TAGCAGGCTGCCCTG | 9100 |
| rs567914190 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84709605 | ATTTAGGGCAGGGTC[C/T]TTGGACTTTTGACTC | 9100 |
| rs567953573 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84735299 | ACACTGATGTAACCA[C/T]ACGTTTTAGTTGCTA | 9100 |
| rs568010157 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84768051 | TTATTTTTAAATTCA[G/T]TATATTTTTGGCTTT | 9100 |
| rs568072319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84707743 | GAAGTGCTGCCACAA[C/T]TTATAACATGTTGTC | 9100 |
| rs568078546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84772204 | TTACAGGCGCCCACC[A/G]CCACGCCTGGCTAAT | 9100 |
| rs568091778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84752001 | TGTGGCAGCCCTTGT[A/G]AGCTACCATCTAGCA | 9100 |
| rs568125135 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84775521 | GTTTGAGAATGTGAC[A/C]TCTCCCGGCTGTGCT | 9100 |
| rs568131698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84703379 | AATGTCATGCAGTTG[A/G]CTTCTGTCCTTGTCT | 9100 |
| rs568137374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84771797 | CGTTTGAACCCGGGA[A/G]ACGGATGTTGCAGTG | 9100 |
| rs568144674 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84723852 | GTTCTGTCATTCCCC[A/G]GAATGACATTGAGCC | 9100 |
| rs568158699 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751624 | TAGTGGTACATTTTG[G/T]TCACTTTGCTGTCCT | 9100 |
| rs568172830 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84778834 | GGGAAGTCGGCGGAG[A/G]CCTGTAATGATTCGT | 9100 |
| rs568192862 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84703726 | GTGAGCCAGTGGTCA[C/T]CTTAGTGGTTTGTAC | 9100 |
| rs568207702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84729821 | GAGTTCAAAACAGCC[A/G]TGGCTAGTGATTTGT | 9100 |
| rs568208747 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719296 | GAAGTAGCTCCCCTC[A/T]TCCTCCTGTTTTCTG | 9100 |
| rs568213579 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84764428 | GATGCTTCCCTTGTC[A/G]GCCCCCGTGGCTTAT | 9100 |
| rs568302327 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84754827 | CATGCAGATTATTCT[C/G]GGCCCCTAACTCAGT | 9100 |
| rs568319387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84778389 | CTTAATCTATTCCAC[A/G]AAAAAATAAATTGTG | 9100 |
| rs568345427 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84759022 | TATGTTGGCACGTGA[A/G]TGAGGGCTGCAGACA | 9100 |
| rs568374511 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84775917 | GAGTCTTTACCTCTT[C/T]GGATTGTTGCTGTTT | 9100 |
| rs568429319 | in-del | -/AAG | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84736562 | GTCACCTTATTTAAT[-/AAG]CATGTTTAAACCTCA | 9100 |
| rs568470240 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84729036 | CTCCTGAAGTCAAGT[G/T]ATCTGCTCGCCTCGG | 9100 |
| rs568476439 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780339 | AGAGAGGGATGTCAC[A/G]TGCAAGGGTGCCCGT | 9100 |
| rs568530999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84721568 | GGTCTTGCTCTGTCT[C/T]CCAGGCTGGAGTGCA | 9100 |
| rs568591047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84759605 | TTTTTTAAAAATAGA[C/T]TGTTGGCGATTTTAT | 9100 |
| rs568595885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84722016 | TGAGTTTTGACAGAT[A/G]TATACACCAAAGTAG | 9100 |
| rs568601831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84764658 | CAACATGGTGAAACC[C/T]CGTCTCTACTAAAAA | 9100 |
| rs568607764 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84742336 | TGTTTCCTGCATCCA[C/G]AAGAATCCTTTTTCT | 9100 |
| rs568641987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84711532 | TTGTTGCTCATGGAT[C/T]CGTCAGGTGAGGAAA | 9100 |
| rs568655139 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717993 | TATAATTTATGGTAT[G/T]TTCAAAGTTCCTTAC | 9100 |
| rs568662616 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84729541 | AGCATATGGGGAATA[C/T]TCATTGTATGGGAGA | 9100 |
| rs568663357 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84764364 | TGAGACTTCTTGGAC[C/G]TAATGGTTTGCATCT | 9100 |
| rs568663398 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84769566 | TGGGGAGGTTGGTTG[C/G]GTGGTTCAGTTGTGC | 9100 |
| rs568663740 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84763836 | ACGTTGTGCCTGTTG[C/G]GATTGGTTGCCATGG | 9100 |
| rs568725184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84769135 | AATTATGGACGGTCC[A/G]TAGCATTCCTGCAAA | 9100 |
| rs568746768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84742670 | CGTCCTGCACTTCGT[C/T]TGCCTGGCACATTGG | 9100 |
| rs568774832 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84711483 | CATAGCATTAAGCCA[A/G]TTTACCATCGGGAAT | 9100 |
| rs568849458 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84760326 | TTGCCTTTTGTTCCA[C/G]TGTTTGTGTGGTAAC | 9100 |
| rs568903081 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84741391 | TTGGCTGATGTCAAC[C/G]TCTCAGACATCTGAG | 9100 |
| rs569087620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84710000 | TTGAGGCCGGGTGCG[A/G]GGCTCACGCCTGTAA | 9100 |
| rs569101082 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84709596 | AAGGAGATCATTTAG[G/T]GCAGGGTCCTTGGAC | 9100 |
| rs569105750 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84772966 | CACTTTTCTGTGAAT[A/G]TTTCAGGGATGAATG | 9100 |
| rs569142354 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84743141 | TACATATGATAATAA[A/G]TTCATTTCCCCTTGA | 9100 |
| rs569164972 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84712415 | TCTGGTATGGTCTGG[A/C]TGCCCCAGTGTCCCC | 9100 |
| rs569205633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84705271 | GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 9100 |
| rs569219109 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84707829 | CACGCCTGTAATCCC[A/G]GCACTTTGGGAGGCT | 9100 |
| rs569243851 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699885 | CCAGGCGGGGCAGGG[G/T]ATGTCCGCGGCCCGG | 9100 |
| rs569289452 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84750291 | CTCATGGCTGTAATC[C/G]TAGCTACTGAGGAGG | 9100 |
| rs569290999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84717069 | CGGGTCTTGTGAATG[C/T]GCACATTTAGATTCA | 9100 |
| rs569296981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84765259 | CACAGTTACCCTTGT[A/G]TGTGTGTGTGTGCAC | 9100 |
| rs569310385 | in-del | -/AAAT | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84774247 | GACTCCATCTCAAAA[-/AAAT]AAATAAATAACATAA | 9100 |
| rs569313400 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84757150 | GTGCTATCTCTGCTG[A/G]GTGTCATCACATGCA | 9100 |
| rs569358413 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84709137 | ACAGGCATTGTTTCT[C/G]TCGCGGAGGAGTTTA | 9100 |
| rs569358825 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84770099 | GTGCGATAGTGAAAC[C/G]GTGTCTCTAAAACAT | 9100 |
| rs569377658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84708751 | CTGACTTGTAATAGA[A/G]TGCAAAATCGGGGCT | 9100 |
| rs569423478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84776851 | AGAGTTTTGCTCTGT[C/T]GCCCAGGCTGGAGTG | 9100 |
| rs569445312 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84777147 | GGAGAAGCAATCTCG[C/T]GCACAAGCTTTTCAG | 9100 |
| rs569456232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84756954 | GAAGCCCCTTATATA[C/T]TGAGGAAAGGGCTCA | 9100 |
| rs569481168 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84772851 | CTTAATACTAAAATT[C/G]TCATGAAAATGGCCT | 9100 |
| rs569509923 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84735997 | GGCGAGGGCGTGTCA[C/G]TTGGACCTGTGGGTG | 9100 |
| rs569512243 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84752688 | ACATAATTCGGTCTG[C/G]TCTTAGGAGGAATTA | 9100 |
| rs569546172 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84702954 | CCGAGATCATGCCAC[-/T]TGCACTCCAGCCTGG | 9100 |
| rs569567924 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84702758 | AGCACTTTGGGAGGC[A/G]CAGGTGGGTGGATCA | 9100 |
| rs569577307 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84752433 | TCAAGTTTCAACCTA[C/G]AAGTTGCCTGCCCTC | 9100 |
| rs569616587 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741450 | CTTTGCACGTGGTGA[C/G]CATGCTGCTCATGTT | 9100 |
| rs569637163 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84710611 | TCCCTTGATTATATT[C/T]GTAGAAAATATTAAG | 9100 |
| rs569643570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84774730 | CGTCTCAGCCTCCCA[A/G]AGTGCTGGGATTACA | 9100 |
| rs569660982 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84738077 | GAAGATGGTGAGCAG[C/G]GTTCTAACAGCTCTC | 9100 |
| rs569670550 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84778265 | TCCTGCCATGTGGGC[C/T]GGCACCGGGAGATTG | 9100 |
| rs569679604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84706684 | TAGCTGGGAATACAG[A/G]TGTGCGCCACCACGC | 9100 |
| rs569685285 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84737068 | GCTGGGATTACAGGC[A/G]TGAGCCACCACGCCC | 9100 |
| rs569740120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84777904 | CCCGCGGAATGCTGC[C/T]GGACAGCCGCCTTCC | 9100 |
| rs569746713 | snp | A/T | 0.000967586 | 0.021974 | intron-variant | USP10 | GRCh38.p7 | 16:84732434 | TTCTTCTCAATGACT[A/T]CTTCTTCTTCTTTTT | 9100 |
| rs569782684 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84750539 | CCTCATTAGCACAGA[-/T]ACTTTGGAGTTGACG | 9100 |
| rs569800787 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84750739 | TATATTTTGTTTTAA[C/T]AGAATATAAATAATG | 9100 |
| rs569802147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84738462 | AGGGTTTTGAACGAG[A/G]TGGAGGCTTCCTGAG | 9100 |
| rs569812214 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84763141 | GTTCGCTGTAAACAG[A/G]TGTTGCATACTCATA | 9100 |
| rs569814071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84732740 | GGCGTGAGCTACTGC[A/G]CCAGGCCTCAATGAC | 9100 |
| rs569860271 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84737256 | AGCACTGTTTTCACA[C/G]TGTGCGTTTAGCATA | 9100 |
| rs569865758 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84757363 | AGTTAGAAGGAAGAG[C/G]ACATTTATTCATAGG | 9100 |
| rs569895039 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84762002 | AACTTTGCAGTTTAC[C/G]TAGATGCTTCAAACA | 9100 |
| rs569900646 | in-del | -/A | | | intron-variant | USP10 | GRCh38.p7 | 16:84701288 | AGCTTCAATTTTGTT[-/A]AATTAGCTGTAGTTT | 9100 |
| rs569938900 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84766713 | CTTGCTGGCTCAGAT[G/T]GAACAGCTCTGTCAC | 9100 |
| rs569954474 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84764676 | TCTCTACTAAAAATA[C/T]AAAAATCAACCAGGT | 9100 |
| rs569983991 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84759148 | TCAAGTTCTTGAATA[C/G]AAACGACTGACTGCT | 9100 |
| rs570057794 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84705702 | AGTACAGACATAATC[A/C]TGCCCTTGCTTGCTT | 9100 |
| rs570069514 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84748440 | TCCCTAGTAGCTGGG[A/C]CTACAGGTGCCTGGC | 9100 |
| rs570071235 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84770591 | TCCTGGCTAACACGG[C/T]GAAACCCCGTCTCTA | 9100 |
| rs570085613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84734940 | GGGCAGTGCATCTCC[C/T]CTGGTTCCGAGTGTG | 9100 |
| rs570092314 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84703842 | CCATCATGCTCTTGA[C/G]CCCATCTCATTGAGA | 9100 |
| rs570143701 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84717027 | AGCAGTGCTTCTCAA[A/G]CTTAAAAGTCCGTTG | 9100 |
| rs570146912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84735301 | ACTGATGTAACCATA[C/T]GTTTTAGTTGCTACA | 9100 |
| rs570208450 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84730378 | TCATTTTCCCCTAGT[G/T]AATTCTGTAATTTGA | 9100 |
| rs570232908 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84733855 | ATATCACCATAGTCA[A/G]TCGTAGTGTTTTATG | 9100 |
| rs570283927 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84771417 | GGAGAATCACCTGAG[A/C]CCAGGAAGTCAAGGC | 9100 |
| rs570292528 | in-del | -/A | 0.365646 | 0.221644 | intron-variant | USP10 | GRCh38.p7 | 16:84710270 | CAGACTCCATCTCGG[-/A]AAAAAAAAAAAAAAA | 9100 |
| rs570377334 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84771823 | CAGTGAGCGCAGATC[A/G]TACCACTGTACTCCA | 9100 |
| rs570404972 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84704376 | CACATGCAAGAATCA[C/T]CATCGCACAAAACAG | 9100 |
| rs570424651 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84763886 | GTTGCGATTGGTTGC[C/G]GTGGATCCAGTGACA | 9100 |
| rs570429490 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84743491 | AAGGTAAAATATATT[C/G]AGTTCTCCGCAGTAG | 9100 |
| rs570490782 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698115 | ATAGCACAGACACTA[C/T]ATTGTATTGTTTTCC | 9100 |
| rs570513363 | snp | C/T | 3.40136e-05 | 0.00412379 | intron-variant | USP10 | GRCh38.p7 | 16:84772734 | TGACACACTCCTGCA[C/T]ATCAGAAGCTCAACC | 9100 |
| rs570557415 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84748459 | CAGGTGCCTGGCACC[A/G]CGCCAGGCTAATTTT | 9100 |
| rs570586311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84725806 | TCTGGTCCAACATAC[C/T]TTCATTTTGTAGATG | 9100 |
| rs570641894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84747250 | TTTGGTTTAGGCTTT[C/T]TGTAATACTTTCTGA | 9100 |
| rs570647136 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84721026 | AGCCTCTCGAGTAGC[C/T]GGGAGTACAGGTGCC | 9100 |
| rs570704124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751246 | CTATACCATCTAGGC[A/G]TGTGATCCCACAATG | 9100 |
| rs570719085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84724478 | ATTGCAGTACTTTGA[C/T]ATTTGAGTTTCAAGG | 9100 |
| rs570731978 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84755151 | AAGTTTCAGGCAGAT[C/G]TTGTATGCCTGGCCC | 9100 |
| rs570746931 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84717132 | AGCTCCTAGGTAATT[A/C]CTAGGCTGCTGGCCT | 9100 |
| rs570788531 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84709901 | AGTGGTTAGCCGGGA[G/T]TCTGGAGAGGAGAGA | 9100 |
| rs570800800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84752400 | GATACACCAATGGCA[A/G]TGACTTTGGAATGCA | 9100 |
| rs570806591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717348 | AAATTTTGTGCAGAT[C/T]AAATGAAATATGTTG | 9100 |
| rs570808395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84712869 | CAAGTGTAGTCTGGA[A/G]ATGATAGGACACTTA | 9100 |
| rs570820060 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84711180 | GATTATGCCTTTTAA[C/G]CAAGCATTTACCCAG | 9100 |
| rs570867161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84776758 | CTCTGCAACCTGCCT[C/T]GCCCCGGGACCTGGG | 9100 |
| rs570909727 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84720142 | AGGAGATTTGAAGAG[A/T]CTGCTGACAGTGGCC | 9100 |
| rs570928412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84776310 | GGGTGAGGGCCTAGC[A/G]GTGGGGGCCCAGGGG | 9100 |
| rs570988892 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84755776 | GCATTCCAGCCTGGG[C/T]GGCAGAGTGAGACTG | 9100 |
| rs570993485 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84756183 | TCCCTTCACTGGTCT[G/T]CGAGCTTGCCTAGGG | 9100 |
| rs570999124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84739097 | AGAGTCTTGTGCTGT[C/T]GCCCAGGCTGGAGTG | 9100 |
| rs571034552 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84733574 | TTCTATTTTAATTTG[-/T]TTTTTTTAAATAAAG | 9100 |
| rs571066035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84765041 | GATTACACCACTGCA[C/T]TCCAGCCTGGGTGAC | 9100 |
| rs571071959 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84760718 | GTACTTGATTCCTTT[A/T]CCTAATTTTTTTTTA | 9100 |
| rs571088820 | snp | A/C/T | 0.000144468 | 0.00849797 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84760211 | ATATTCGCCCTGGAG[A/C/T]TGCCTTTGAGCCCAC | 9100 |
| rs571128811 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84764672 | CCCGTCTCTACTAAA[A/C]ATACAAAAATCAACC | 9100 |
| rs571153257 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84708290 | CCTCATCTCTGCTAA[A/T]AATACAAAAATTAGC | 9100 |
| rs571195350 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84752739 | TTTTTTTCACTGCGA[A/G]GAAGAAGAGGAGCTC | 9100 |
| rs571223268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84727338 | TACAATTTTCCCCCC[C/T]CATGTGACAGCCTTT | 9100 |
| rs571241177 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718336 | ATGGCTCACTGCAGC[C/G]TCAAAGTTATTGGCT | 9100 |
| rs571288086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84743992 | CAGCGGAGGAGACCA[A/G]GAGATAGAGAATTCA | 9100 |
| rs571352692 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84704694 | GATGTAGAATCTTCA[C/G]ATCCTAGATTTTTTC | 9100 |
| rs571381236 | snp | C/T | 1.7009e-05 | 0.0029162 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745149 | CTGTCAGTGACATTG[C/T]GCCTGACAGTCCTTT | 9100 |
| rs571399017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741092 | CCAAACTTTTTCTTT[A/G]AGAGTTAGAGGTTTG | 9100 |
| rs571428921 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84740066 | CATTTTTATTCCTTT[C/T]GGCTTCATTTTCGGA | 9100 |
| rs571450898 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84774691 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG | 9100 |
| rs571456595 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84737553 | CACAACCCATCTGGC[A/T]TTCCTGCAGGTGCGC | 9100 |
| rs571476786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84706134 | GGATCCCTTCTGCTT[C/T]AGCTTCCTAAAGTAC | 9100 |
| rs571495215 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84769249 | ATGACTGGGATGGAT[C/G]TATCCTTGGCTTATC | 9100 |
| rs571500765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84769662 | CCCTGGCTGCTGGTG[C/T]ACTCTGCTTATGCTG | 9100 |
| rs571559994 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84700479 | GGCGGCCCGGGGGCT[C/G]CGGGAGTCCCCTGGA | 9100 |
| rs571563803 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84773642 | CCGTTGCTCCTCTCA[C/T]ACTTCTAGCTGCCTT | 9100 |
| rs571578874 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84777462 | GGACATGCTGCTGTC[A/C]TGGGTGCTTCCTGCC | 9100 |
| rs571590538 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84743763 | ATAAAAATACGTCTG[C/T]CTTAGCAGGAATGAA | 9100 |
| rs571629211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84762044 | AGGGCCTTGGAATAG[A/G]CAGTTGTGCTGTGAA | 9100 |
| rs571633923 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | USP10 | GRCh38.p7 | 16:84770766 | GACAGAGCGAGACTC[C/T]GTCCCCAAAAAAAAA | 9100 |
| rs571650966 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84729202 | AAAAATGATGTCTTA[A/G]CCTTCACATTTGTAT | 9100 |
| rs571659358 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84762379 | ACAGAAACTTTTTTT[A/T]AAATAACTTTTTTGT | 9100 |
| rs571716214 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84736610 | TTTATGTTCAGAAAG[A/G]AAGAGAAAATGCTCA | 9100 |
| rs571717882 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84736023 | GGGTGTGTGAGTGGC[A/G]AGGGCGTGTCACTTG | 9100 |
| rs571738238 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84705209 | AAAAAGGTGAGTGTC[A/C]CCACTCCTGTGCCTT | 9100 |
| rs571740137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84704922 | ATTCCTCGACTTTCC[C/T]TTTTGGGCTCACATG | 9100 |
| rs571778688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84770843 | GAGGCTGAGGCAGGC[A/G]GATCACAAAGTCAAG | 9100 |
| rs571897906 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84731770 | CTTTCATGATCTCTG[A/C]TAGCTCTTTTTTTTT | 9100 |
| rs571914999 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84748493 | ATTTTTAGTAGAGAC[C/T]GAGTTTCACCATGTT | 9100 |
| rs571916210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84749537 | TTGAGCCCGGGAGTT[C/T]GAGGCCAGCCTGGGC | 9100 |
| rs571923801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84733037 | CATTTGAACCACGTT[C/T]TCTGCTTTTCTTTAG | 9100 |
| rs571946294 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84708942 | AGAGGTTCGCTGGGT[A/G]GTGAGGGAGAGAAGC | 9100 |
| rs571960354 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84766799 | TCTTTTTGAAAAACG[G/T]TAAAGCAAAGATAGG | 9100 |
| rs571961037 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84726824 | TTGCTCCCCCGAATC[G/T]CAGGCATTTCTGTGC | 9100 |
| rs571982875 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84738112 | TTGTGAAGTGGATGG[A/G]TGAAGAGGTCCCTTC | 9100 |
| rs572024297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84770850 | AGGCAGGCGGATCAC[A/G]AAGTCAAGAGATCGA | 9100 |
| rs572044260 | snp | G/T | 1.65954e-05 | 0.00288053 | missense, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84733495 | GTGACTCCTCGATCT[G/T]CAGTTGAGGTAAGAC | 9100 |
| rs572087423 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84766002 | TAATTTCCTTTCTGA[C/G]GCCTTGCGGCATAAC | 9100 |
| rs572114900 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84728111 | ACCAAACACCTAAAA[G/T]AACATTTGATTGGAA | 9100 |
| rs572143490 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718848 | CCCAGGCTGGAGTGC[A/G]GTGGTGCAGTCTCAG | 9100 |
| rs572149616 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | USP10 | GRCh38.p7 | 16:84770652 | TGGCAGGCGCCTGTA[A/G]TCCCAGCTACTCAGG | 9100 |
| rs572164092 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84714464 | GCTGGGGCTACAGAC[G/T]TGCGCCACCGTGCAC | 9100 |
| rs572173130 | snp | C/T | 0.000713462 | 0.0188738 | intron-variant | USP10 | GRCh38.p7 | 16:84775110 | TTTCTGCTGCTGTTA[C/T]CCTGAACCTTTCTAA | 9100 |
| rs572178470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84750007 | CCAAGGGAAGGATGT[A/G]TCTAAACACAAAAGC | 9100 |
| rs572205967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84754938 | TTGAGGCCAGGAGTT[C/T]GAGACCAGCCTGGCC | 9100 |
| rs572214559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84774758 | ACAGGCGTGAGCCAC[C/T]GTGCCTGGCCTGTAA | 9100 |
| rs572234409 | snp | A/T | 0.000185703 | 0.00963415 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745323 | CCGATACTACTGAAA[A/T]CCTTGGAGTTGCTAA | 9100 |
| rs572294266 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84741222 | CTCCAGTAACATCAG[C/G]GAGTGATTATATCTA | 9100 |
| rs572294530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84745782 | ATTACCTGTGTGTTA[A/G]TAGCAACGTCTGAAG | 9100 |
| rs572296821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84724597 | AATTTTGCTATAGCC[C/T]TATTAGTGAGGGAAC | 9100 |
| rs572332385 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84746474 | CTCCCGGGCTGCAAA[A/C]CTGTCCAGCGTGTTA | 9100 |
| rs572357058 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84741509 | GTTCCCATGCACATC[A/C]CTTCTTTGAGTTCAC | 9100 |
| rs572369848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84722389 | TGCTGTTCACATTCA[C/T]GTACAAGTGTCTGTG | 9100 |
| rs572374005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84722833 | AGTGCTGGGATTACA[A/G]GTGTGAGCCACTGCG | 9100 |
| rs572395195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84746866 | GACTCTTTCATGAGA[A/G]CATTTAGCTTAAAAC | 9100 |
| rs572424578 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84723237 | TGGATCACATGGTAA[C/T]TGTTAATGATTTTTC | 9100 |
| rs572426616 | snp | C/T | 4.97814e-05 | 0.00498881 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744696 | CCAGTGACACTTTGC[C/T]GAGAACCCCCAGCTA | 9100 |
| rs572439647 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751056 | TAATGATGTTTCAGT[C/G]AACAACAGACCGCAT | 9100 |
| rs572472911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84725513 | TCAAGCAATTCTCCT[A/G]CCTCAGCCTCCTGAG | 9100 |
| rs572473991 | snp | C/T | 0.000337433 | 0.0129847 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84778944 | CCATTACACTACAGA[C/T]GTCTTCCAGATCGGT | 9100 |
| rs572482720 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84778617 | AGTGTCTGTGTGAGG[C/T]GTGGGACATTTTAAA | 9100 |
| rs572535843 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84720831 | TCATGATCTGCCCAC[C/T]TCGACGTCGCAAAGT | 9100 |
| rs572627857 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84743323 | CACCCTTCACCCCCC[A/C]CAGTCGGGGGCTGTG | 9100 |
| rs572691944 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | USP10 | GRCh38.p7 | 16:84714929 | ATTATTATTATTATT[A/T]TTATTATTTTTTTTT | 9100 |
| rs572699618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84706412 | ACAAAGAGTTCCTAT[A/G]TACCCCTTCTCTTGG | 9100 |
| rs572701948 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84710194 | AGAATCGCTTGAACC[C/T]GGGAGGCAGAGGTTG | 9100 |
| rs572703115 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84776414 | TTGTTCCTTTTGACT[C/G]TCTTCTTTTCTCCCC | 9100 |
| rs572711968 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84711919 | GAGACGGGGTTTCAC[C/T]ATGTTGGCCAGGCTG | 9100 |
| rs572762595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84710738 | TTTTAGGTTTGTGAT[C/T]CTCGAGTGCCCTCTT | 9100 |
| rs572842212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84755844 | CTTTTAATATACATA[C/T]ACGATTTACTGGTGT | 9100 |
| rs572842841 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84772027 | TCTGCAGTTGTGCTT[A/C]TGGGAACGTATGCAT | 9100 |
| rs572843301 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84743917 | CCAGTGTGAATTTAT[G/T]TAGAGGACGTTTGCA | 9100 |
| rs572901455 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84755430 | AGCAGCCTGCACTTG[A/C]TGTCTTCACTCCTAC | 9100 |
| rs572903480 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84760030 | GGTAAATTCAGTCTT[C/G]TTGGGAAGATAGTGT | 9100 |
| rs572906468 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717219 | GTGAAGTTCTGAAAT[C/G]ATACGCAGAAATGTG | 9100 |
| rs572947672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84763719 | GATCAAGTGGCATTG[C/T]AATGGGTTGCAGTGG | 9100 |
| rs572968910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84712921 | CACCAGAGTTACCAG[C/T]AAGTGCTTGGCTGTG | 9100 |
| rs572987255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84711990 | CTCCCAATGTACTGG[A/G]GTTACAGGCATGAGC | 9100 |
| rs572992851 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84774934 | CAGCCTCGGCCGTTG[C/G]TCCTGTTTCTTTAGT | 9100 |
| rs573029102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84712594 | GGCATGAAGTTCAGG[A/G]CCACAGCATGCAAGA | 9100 |
| rs573031336 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84748794 | CTGTATATGTTAAAG[A/T]CTAATTGAAGTAGCT | 9100 |
| rs573033157 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84727890 | TTTTTTCTAACCTGT[C/G]CATATTCTAATTTTG | 9100 |
| rs573034659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84767641 | GTGCAGTAAATAACA[A/G]TGTGGAGAGGAAGTG | 9100 |
| rs573038921 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84742535 | GTACTGCAGTGAGCA[C/G]CCTTGGAGAAATGCT | 9100 |
| rs573048170 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84707896 | CCAGCCTGGGCAACG[C/G/T]AGCAAAACTCTTTCT | 9100 |
| rs573062619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84722228 | TGTTTGGTTACCTTC[A/G]CCTGACCCAACTATT | 9100 |
| rs573144258 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84715878 | GCTAGTTTCCCCCAC[A/G]ATGGCGGAATGGCCA | 9100 |
| rs573146495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84760388 | AGCGCTATAAGTAGA[C/T]GTAGGTTTATAAGAG | 9100 |
| rs573158942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84708880 | TTCACAGATTTTGGT[A/G]GCCGGACGTTAGGAG | 9100 |
| rs573204665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84725186 | TTCATTAGCAGTCAC[C/T]GCCTCCCGCTCCCCC | 9100 |
| rs573220328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84704615 | GAAAATAAAGGTAGC[C/T]CTTGGGGTATGTGTA | 9100 |
| rs573326518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84742718 | ATGCGGTGCAAGGCA[C/T]ATGGCGTCCATTGTG | 9100 |
| rs573366256 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84773909 | TATCTTTTCTTGCTT[C/G]CTGTATTTTTATATC | 9100 |
| rs573384145 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84705483 | CGATCCGCCCACCTC[C/G]GCCTCCCAAAGTGCT | 9100 |
| rs573384486 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84710079 | GTTTGAGACCAGTCT[C/G]GCCAACATGCTGAAA | 9100 |
| rs573387147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84739113 | GCCCAGGCTGGAGTG[C/T]AGTGGCACTATCTCG | 9100 |
| rs573404787 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84752782 | AAGCGTTAGTGTCTC[C/G]TCCAGTTGATGGTTA | 9100 |
| rs573413587 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84773512 | GCCGGCTCCCTGTCT[A/G]CCCTAGGGGCGCCCT | 9100 |
| rs573456984 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698634 | AGAGACTCGCTCTGT[A/C]ACCCAGGCTGGAGTG | 9100 |
| rs573466081 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84752507 | CCATAATTGGAATGC[A/G]TATTGGACTTTAGGC | 9100 |
| rs573481171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751756 | CAGAAAAGCAGGTCA[A/G]CAACACCAGAATGTC | 9100 |
| rs573505240 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84723916 | CCCAGCAAAGATAGA[A/C]CTGCTTCTGTTACAG | 9100 |
| rs573526767 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | USP10 | GRCh38.p7 | 16:84756652 | CTTAAGGTTAGGTTT[A/T]AAAAAAAAAGTCATT | 9100 |
| rs573591256 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84756400 | GAGTTCAAGACCAGC[C/G]TGGCCAACATGGTGA | 9100 |
| rs573595279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84722843 | TTACAGGTGTGAGCC[A/G]CTGCGTCCGGCTCAG | 9100 |
| rs573618542 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84777210 | CAGGTGTGAGTGACA[A/C]ACGGCTCAGCCCAGG | 9100 |
| rs573629120 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84704573 | GACCATTTCTGTCAA[A/T]ACAGGCTGGATGAAG | 9100 |
| rs573725057 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84700689 | CTGTTGCAAAGAAAA[C/G]TCGAAATAAGTCGCA | 9100 |
| rs573728189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84732523 | GCGATCTCAGCTCAC[C/T]GCAACCTCGGCCTCC | 9100 |
| rs573729550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84736859 | AGGGGCGTGATCTCG[A/G]CTCACTGCAAGCTCC | 9100 |
| rs573729610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741140 | GCATGGTCAGACTTA[C/T]GAAAGGGGTTTTAAT | 9100 |
| rs573754528 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84752967 | TTATTTTTTAAAAAC[A/G]TATTTTTTTTTTCTT | 9100 |
| rs573843199 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84745865 | GGAGGAGAGGGTTGT[C/T]GTAACTTTATGTTAA | 9100 |
| rs573902135 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84736155 | TATCTCTCAGGTAAC[A/G]TAATTGCCGCTCAAA | 9100 |
| rs573907253 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84720243 | GCCGTGGCGATGTGC[A/G]TTCCTTCCTGGCGGG | 9100 |
| rs573971339 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | USP10 | GRCh38.p7 | 16:84770543 | TTTGGGAGGCCAAGG[C/T]GGGTGGATCACGAGG | 9100 |
| rs573978089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84777750 | GCCCCTCCACGTGAC[A/G]ACTGCGACTAGAACC | 9100 |
| rs573986676 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699607 | TCGGGGATCTAATGC[A/G]AACACTCCCGAGGCC | 9100 |
| rs573990436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84731322 | GTTGCAGAGCAGGGC[C/T]ACGCCATAGGCAATG | 9100 |
| rs574023347 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84700002 | CGGCGGCCGATGCGA[C/G]TGTGTATGTGCGGGC | 9100 |
| rs574028070 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84704127 | TGGTATCATCTCCAA[C/T]TGAATTAGTTACATC | 9100 |
| rs574029562 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84734729 | CCATCCTTTAGATAA[C/T]GAAGATATTTGTCTG | 9100 |
| rs574034942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84770217 | TGTGGTGGTGTGTTA[C/T]CAGATGAGGCCAGGA | 9100 |
| rs574050532 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84754258 | TAATAACAGAATGAT[A/G]CGGTATTTTAGTTTA | 9100 |
| rs574069410 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84734151 | TGGGAATGGAATTAC[C/T]GGGTTCTGTGGACCG | 9100 |
| rs574106741 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84761781 | TTATTGGACCGATGG[G/T]AACCTTTCTGAAATC | 9100 |
| rs574111479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84753572 | TGCGGAGTGATCTGC[C/T]GCACAATGAATGAAG | 9100 |
| rs574113373 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84758073 | GAAAGAGTGATGTCC[A/C]CTCAGGGTGAACCTG | 9100 |
| rs574165379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84765970 | ATCGAAAGTACTGAA[A/G]AGGCCTCATTGGAGC | 9100 |
| rs574174476 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84757543 | AAGCTTATTTTTGAG[C/T]GATGCCTTAGATGGA | 9100 |
| rs574184576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84726579 | TTGTTCCCATCCCTG[C/T]TGTGGTGTGGGCTTG | 9100 |
| rs574244037 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718121 | GAAAATCTTGGATTG[G/T]AAGGTTATTTTTGAG | 9100 |
| rs574244824 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84730126 | TCCACTCCTGTCTGC[A/G]TCCACTCAGCGTCCA | 9100 |
| rs574251730 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84765439 | TCCCACTCGCCACCC[A/C]TAGGAACCACTCTTT | 9100 |
| rs574252434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84721811 | CAAGCAATTCTCCTG[C/T]CTCAGCCTCTCGAGT | 9100 |
| rs574268099 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84713477 | CCCGCTATCCTGACG[C/T]GTGTGTCTGGTTCAC | 9100 |
| rs574275066 | snp | A/G | 4.9802e-05 | 0.00498984 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744821 | AGCTATGGCTCCATC[A/G]ACTGCCAGTACCCAG | 9100 |
| rs574327082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84763267 | AATTACAGTTTATCC[C/T]GAACCTCTGCCATTT | 9100 |
| rs574365579 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84762867 | CATCATGTCATTGTT[G/T]GGAAATACTTTACAT | 9100 |
| rs574495039 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84703070 | TTAATAACCTTATTT[C/G]CAAATATTAGAAAGT | 9100 |
| rs574562288 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84766855 | TTTCAGCCATTGTTA[A/C]GCATGATTCTTTATT | 9100 |
| rs574565863 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84715945 | GTCACACCAGCCTGA[C/G]CAAGAGAGTGAGTGT | 9100 |
| rs574569342 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | USP10 | GRCh38.p7 | 16:84760491 | GAATAAAGTATGATT[A/G]TGGTCTCCTTGTTAC | 9100 |
| rs574575542 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84775033 | CAACTGAAGGGATAG[A/T]GTGTTGTTTTGTTCC | 9100 |
| rs574579190 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84724632 | CTTCTCTTCCTCCTT[A/C]TTCCTTTGTCTGCTT | 9100 |
| rs574585894 | in-del | -/A | 0.0652144 | 0.168387 | intron-variant | USP10 | GRCh38.p7 | 16:84714932 | ATTATTATTATTATT[-/A]TTATTTTTTTTTTTT | 9100 |
| rs574619032 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84774776 | GCCTGGCCTGTAATT[A/G]AAGTTTTATGATCTG | 9100 |
| rs574623903 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84771460 | TCATCATGCCACTGC[A/C]CTCCAGCATGGGCAA | 9100 |
| rs574624981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84711641 | TCTGTGCCACAACAA[C/T]GTATTCTAAGTTAGG | 9100 |
| rs574644532 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719948 | CTTTTATTTTCAACA[A/G]ATAGTAATTTTGCAG | 9100 |
| rs574647797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84750054 | TTGGAGAGGGATCTG[C/T]GTTTCAGTGACTGGT | 9100 |
| rs574660334 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP10 | GRCh38.p7 | 16:84751075 | AACAGACCGCATGTA[C/T]GACAGTGGTCCCATA | 9100 |
| rs574675650 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | USP10 | GRCh38.p7 | 16:84773528 | CCCTAGGGGCGCCCT[A/G]TACCTTCCCGTGAAG | 9100 |
| rs574678554 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84741938 | GTAAGCCCTCAGTAC[A/T]TTTGTTGGATGAATG | 9100 |
| rs574678702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84737831 | GTGCCTGGCACACCC[C/T]GAGTGCCCAGTCAGT | 9100 |
| rs574679996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84778087 | TTTTTTTTTAAGTAA[A/G]TAACTGTGTGTGTGT | 9100 |
| rs574695538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84770985 | TCACTTGAACCCTGG[A/G]GGTGGAGGTTGCAGT | 9100 |
| rs574700820 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84731201 | AGCCAGGATGGTCTC[A/G]ATCTTCTGACCTCAT | 9100 |
| rs574703831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84720324 | AAGTGAAAAATCCTG[C/T]AGAACAGATGGCACT | 9100 |
| rs574741379 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84738164 | GCCTGCTGCAGTCTC[G/T]CGGGTCTGGAGGTTT | 9100 |
| rs574767932 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84716304 | TTAAATATTATTGTT[A/C]CTTAACTGTTAATGT | 9100 |
| rs574785043 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84754715 | CTGTCTGACTAGTTC[A/T]TGCTGTCTCACAAAT | 9100 |
| rs574788052 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84772433 | AGTCCTGCCACAGGA[C/G]TCTTGGGCCTCACCT | 9100 |
| rs574799604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84745837 | TAAAAGTAAGATAAT[A/G]TAGAAACAAATGGGA | 9100 |
| rs574817757 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84747418 | GCAATGTATATATAT[A/T]TTTAAGAGTATTTTA | 9100 |
| rs574819354 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84714975 | TGCTCTGTCGCCCAG[C/G]CTGGAGTGCAGTTCG | 9100 |
| rs574850151 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84721084 | TTTTTAGTAAAGACG[A/C/G]GGTTTCACCACTGGC | 9100 |
| rs574850354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84775625 | CCCCCAGCCGGTGAT[C/T]CCTGCGTCCTCCCCC | 9100 |
| rs574862595 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84763178 | GTTGCTTCCCTGCCC[C/T]TCAGTCGTTTTCCTT | 9100 |
| rs574897752 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84778629 | AGGCGTGGGACATTT[C/T]AAATATGTGGTTAAT | 9100 |
| rs574899328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84746381 | GATGGATATGTGTTC[C/T]GAGATGTGCGTGTTA | 9100 |
| rs574946598 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780160 | TCTCCCCTTCCCCTC[C/G]TCATCCCTTGTTTCT | 9100 |
| rs574996893 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84711267 | TTTAAAAATGTAAGT[A/C]CACATGTGTTCCCCA | 9100 |
| rs575012034 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779573 | TACTTCAAAAGAAAA[A/G]TAAACATAAAAAATA | 9100 |
| rs575043267 | snp | A/G | 3.32519e-05 | 0.00407736 | intron-variant | USP10 | GRCh38.p7 | 16:84733541 | TGAGTCCGTGGGTAG[A/G]TACAATTAATAGTTA | 9100 |
| rs575044511 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84737040 | TGGTCTGCCCGCCTC[A/G]GCTTCCCAAAGTGCT | 9100 |
| rs575068027 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84776243 | CCTCAGCTCACGCCC[A/G]ATGTTTTAGGAAGTT | 9100 |
| rs575074891 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84710058 | ACGGATCACTTGAGG[G/T]AAGGAGTTTGAGACC | 9100 |
| rs575079575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84735792 | TTTTAACATACGGTG[A/G]AGTTTGGAGGGGTAT | 9100 |
| rs575112323 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84708715 | GTCCCACTCCTGAGA[C/G]ATAACCACATTTAAG | 9100 |
| rs575115150 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84774397 | AGAGCAGGGAGTTCC[C/T]GCCTCGTAGCAGCTG | 9100 |
| rs575128135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84776067 | ATTGACCTTCACACA[C/T]GTATTGAACCTCTTC | 9100 |
| rs575160637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84756252 | CGGTGCCTAGGCAGG[A/G]CTCAGCAGGGGTTTA | 9100 |
| rs575177304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84768712 | GTAGGGTACAACTGT[C/T]ATTAGATTAGTTAGG | 9100 |
| rs575239169 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84708047 | TGTGCCACTGCACTT[A/C]AGCTTGGGTGACAGA | 9100 |
| rs575243127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84758101 | CTGAGGCTGAGCAGC[A/G]TGTTTGTAAATGGAA | 9100 |
| rs575256771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84743758 | AAACTATAAAAATAC[A/G]TCTGTCTTAGCAGGA | 9100 |
| rs575265183 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84721898 | AGACAGGGTTTCACC[C/G]TGTTGCCTAGGCTGA | 9100 |
| rs575281582 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84748080 | AATGGCGTGAACCTG[A/G]GAGGCGGAGCTTGCA | 9100 |
| rs575291819 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84713364 | GGCCATCTTCTTACA[C/T]CCACTTTACCCACCT | 9100 |
| rs575339503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84708926 | AGAATTCCTGTGCTT[C/T]AGAGGTTCGCTGGGT | 9100 |
| rs575352434 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84709202 | TAATCACAGTTACGT[A/T]CACGTCACTCCAAAC | 9100 |
| rs575354856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84760070 | TATGCCATTCTCAAC[A/G]TTCAGCCAGGTGGGA | 9100 |
| rs575363812 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84704073 | GGCACGTTGCACTGT[G/T]CTGTGCTCAGAATAT | 9100 |
| rs575386460 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84737605 | CAAAGTAAGTGTGTT[C/G]AGCATGCTTACTGAA | 9100 |
| rs575487855 | in-del | -/T | 0.484841 | 0.0857308 | intron-variant | USP10 | GRCh38.p7 | 16:84701938 | ATAATTTTCTTCTTC[-/T]TTTTTTTTTTTTTTT | 9100 |
| rs575514076 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84704663 | ATCAGAAAATGTAGA[A/C]TTTATCATAAACCTC | 9100 |
| rs575527077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84720877 | CTGGGCCACCGCGCC[C/T]GGCCAATGATGCACA | 9100 |
| rs575549733 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84739175 | GCCATTCTCCTGCCT[C/G]AGCCTCCTGAGTAGC | 9100 |
| rs575552745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84756743 | ACTATGCCTTTACGT[C/T]ATTGATGGTTATTTG | 9100 |
| rs575615792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84760885 | TGTGATGAATCAGTA[C/T]AAGCAGTTGAAATGA | 9100 |
| rs575655951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84729700 | GCTGAAGTGTAACTG[C/T]TCACTTTTAAAAGCT | 9100 |
| rs575692274 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84739127 | GCAGTGGCACTATCT[C/T]GGCTCACTGCAAGCT | 9100 |
| rs575732800 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84778473 | TTCCGTTTTTTCACT[G/T]TTATAAATGACATCA | 9100 |
| rs575739161 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84749687 | CCCCTATTGTTAAGT[C/G]TGCTTAATAAATGCC | 9100 |
| rs575757520 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84776922 | GGTTCAAGTGATTCT[C/T]GTGCCTCAGCCCCCC | 9100 |
| rs575763414 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84701766 | ACGTTTTATACAACA[G/T]TCTAAAGCGTTATAC | 9100 |
| rs575785599 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699056 | GAAACCAATAGTAAT[G/T]GTTATTAATAACAAT | 9100 |
| rs575793476 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84764800 | GCGCCATTGCACTCC[A/G]GCATGGGTGACAGAG | 9100 |
| rs575795646 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84751397 | CTTGGGGGAAATGGT[A/T]TCTCAGATATTTTGC | 9100 |
| rs575864843 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84752862 | AAGTGGACCTTAAAT[A/G/T]TTTCTTGAGTGTTTG | 9100 |
| rs575928146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84776489 | GCCATGGGCACCACG[C/T]GCTTGTGGGTGTCTC | 9100 |
| rs575952287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84705910 | TATTTTTAGTAGAAA[C/T]GGGGTTTCACCATGT | 9100 |
| rs575958516 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84770589 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 9100 |
| rs575965387 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84769948 | TTTGGATGAAGGCTT[C/G]CAGAAAGAAGGCGGG | 9100 |
| rs575997470 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84773161 | GTCAGGTCACGGGCT[C/T]GGCACTTTTTGAAAG | 9100 |
| rs576028833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84774615 | AGCTGAGACTACAGC[C/T]GCGTGCCACCACGCC | 9100 |
| rs576060598 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84734787 | TTTTCACGCTTCAGT[G/T]TGTAATAAGCTGAAA | 9100 |
| rs576091057 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84737321 | CTTTGCATTTGTCTA[G/T]GGAATTTTATGTCTT | 9100 |
| rs576095842 | in-del | -/TT | | | intron-variant | USP10 | GRCh38.p7 | 16:84764025 | CGACAGATCTGTGCC[-/TT]TTTTTTTTTTTTGCT | 9100 |
| rs576096793 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84727712 | TGCAAATATACAGAC[A/G]TACAATATTTTTCCA | 9100 |
| rs576123909 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719922 | TTAGCTAGTATACCA[A/C]TTTTTGCATTCTTTT | 9100 |
| rs576130368 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84728020 | TGTAGTCTGGAAGTT[A/T]CCCACAGCCTTTCAG | 9100 |
| rs576150784 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717655 | GTTATTGCAGATACC[C/T]AGGCATAGGTGGAGT | 9100 |
| rs576160121 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84763544 | TCTCCTGCGTAACCA[C/G]AGTCCCTTATCTAAC | 9100 |
| rs576191853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84723598 | GGGTTTTTTCATCTT[C/T]CTCTTCCTGAATTCA | 9100 |
| rs576213379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84732997 | GATCATTAACATTTT[C/T]CTTTTTTGGATTTCC | 9100 |
| rs576249818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84762352 | CTTCGTCTTCTATTT[C/T]GTTTACCCAAGACAG | 9100 |
| rs576260837 | in-del | -/CTC | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698313 | GCATTATGGCCTTCA[-/CTC]CTCAACTCTTCAGAA | 9100 |
| rs576285756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84723919 | AGCAAAGATAGAACT[A/G]CTTCTGTTACAGTTT | 9100 |
| rs576378247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84765988 | GCCTCATTGGAGCCT[A/G]ATTTCCTTTCTGAGG | 9100 |
| rs576394808 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84727036 | CCGCAGCAGTGTCAC[A/T]GTTTCTGTGGTGTGG | 9100 |
| rs576402233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84729606 | CGCCTTGCAGAGATG[C/T]TCTTAAACCCTTGGC | 9100 |
| rs576414333 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84754656 | AAGCAAACTGGAAGC[A/T]GGTATCGATTTAAGG | 9100 |
| rs576434887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84745905 | CCATGTCTGTTAGCA[A/G]TTCTTTTCTGTTGAC | 9100 |
| rs576455930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84754329 | GAATAATCATTAAGA[A/G]AAATCTAGGTTGTTC | 9100 |
| rs576458156 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84722248 | ACCCAACTATTTAGA[A/T]TTAGCCATGTTGAGT | 9100 |
| rs576496320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84700571 | GGGGGTGCCCTGTTG[C/T]CCCTTTGCCCCAAGA | 9100 |
| rs576539746 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84750130 | AAACTTAATACAGCC[A/C]GGCACAGTGGCTCAC | 9100 |
| rs576594435 | in-del | -/CA | | | intron-variant | USP10 | GRCh38.p7 | 16:84770772 | GCGAGACTCCGTCCC[-/CA]AAAAAAAAAAAAAAA | 9100 |
| rs576615635 | snp | C/G | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745242 | ATTTTGGTCAGTCCT[C/G]CTTCCCTGCAGAGGC | 9100 |
| rs576631351 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84740900 | CTAAGCTGATTGCCA[C/G]AGATGGTGCTTATGG | 9100 |
| rs576704589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84710130 | CAAAAATTAGCCGGG[C/T]GTGGTGGCGCATGTC | 9100 |
| rs576722562 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84776656 | CCTGGAGGCTCTTGC[A/G]GGGGACATCACTGGG | 9100 |
| rs576724876 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84755029 | TTCAGACAGAGCTTA[C/G]TGCAGCCAGTTCTTG | 9100 |
| rs576730349 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84713977 | AAGGTGGATGGGTGC[A/G]TCTTGTAGGCTCTGC | 9100 |
| rs576733291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84713879 | GGGCGCCCAAAGCAG[A/G]AAGACCTGGCGTGTG | 9100 |
| rs576733432 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718480 | AGTTTTTCTTCTGGC[C/T]GGGTGCGGTGGCTCA | 9100 |
| rs576745376 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84728390 | TGTTGCCCAGGCTGG[A/T]GTTCAGTGGTGCGAT | 9100 |
| rs576747065 | snp | G/T | 3.34292e-05 | 0.00408821 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745368 | AATCCTCGGGTGAGG[G/T]CACAGCTACCAACGG | 9100 |
| rs576777409 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84757174 | ACATGCAGGCTTGGG[A/G]TTCAGTTCGTAACTG | 9100 |
| rs576785758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719358 | AGTGATGGAGCTTTT[A/G]CTTGGATCACGGGAA | 9100 |
| rs576787642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84715071 | GTAGCTGGGACTACA[A/G]GCATGCACCACCATG | 9100 |
| rs576790596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84720023 | ATTAACAACAAAGCC[A/G]CTCATTAAGGTGGAA | 9100 |
| rs576794037 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84714328 | CCCACTTCTTCCTCT[G/T]TTTTAGAGATGGGGT | 9100 |
| rs576864822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84759644 | TAACCAGAAATGGAA[C/T]TGGAGCATTGATGAT | 9100 |
| rs576885608 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84713704 | GGGAAAGAAGCTAGA[G/T]AATCAACTGTTAGGA | 9100 |
| rs576977027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84771885 | CCAAAAAAGGCGGGG[A/G]AGTCAGTACATAAAT | 9100 |
| rs577018223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84739220 | CCCACCACCATGCCC[A/G]GCTAATTTTTTGTAT | 9100 |
| rs577035342 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84771496 | GTGAGATCCTGTCTT[A/T]AAAAAACAAACAAAC | 9100 |
| rs577075164 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84716506 | AGATAACAGTTCATT[C/G]ACAGAGACATAGGTA | 9100 |
| rs577079165 | in-del | -/TAATAAATG | 0.00358779 | 0.0422022 | intron-variant | USP10 | GRCh38.p7 | 16:84729130 | TTGGAATAGTGTTGA[-/TAATAAATG]CTTCTTCATTGTAGT | 9100 |
| rs577083902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84739685 | TATTTTTGAGATAAC[C/T]TTTCAGCTTTTTACA | 9100 |
| rs577096268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84775062 | CCTGGTCTGACAGGC[A/G]GTTTACTTGCTGGGG | 9100 |
| rs577097113 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | USP10 | GRCh38.p7 | 16:84738676 | TGGTGGTGGAGATAA[C/G]TGCAGCTGTCAACTC | 9100 |
| rs577119030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84766923 | CTTCAGATGTTTTTC[A/G]GTTTCCCCAGGAAGA | 9100 |
| rs577166601 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84776586 | CCTTGGAGTGTGGCA[C/T]CCAGGTCCCAGTGGG | 9100 |
| rs577197243 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84712490 | GTTAATTGGCAGGGA[A/C]CAGTTGAAGCAAACA | 9100 |
| rs577243415 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | USP10 | GRCh38.p7 | 16:84711317 | GGCTGTTGCTCTGCA[A/C]CCCACATCTTGAAAT | 9100 |
| rs577287245 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84776612 | GTGGGTGGCCAGCAG[A/T]TTCTCCGCCTTCTCC | 9100 |
| rs577305776 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84709247 | CAAAGGAAGGGAACA[C/G]AATCTGAAGTCAGAG | 9100 |
| rs577305837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84713733 | GATCCAGAATTAGAG[A/G]GACCATCACAGGAGA | 9100 |
| rs577306777 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | USP10 | GRCh38.p7 | 16:84706831 | AGGCGTGAGCCACCG[C/T]GCCGGGCCAAGACTA | 9100 |
| rs577325138 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84706742 | AGACGGGGTTTCACG[G/T]TGTTAGCCAGGATGG | 9100 |
| rs577347999 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84738711 | AGGTGTTGGCTTCTT[A/T]TGAATTGCCCTGTGT | 9100 |
| rs577370660 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84707369 | TACATTTTAATAAAG[A/T]CGTTTATTTTATTTT | 9100 |
| rs577399943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84751378 | CATATATTTCCCCCC[A/G]CTCCTTGGGGGAAAT | 9100 |
| rs577459491 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84732142 | CCCTGTGCATTCTTA[C/G/T]CAGGAGGGTATTACA | 9100 |
| rs577461989 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84755344 | CACCCAGAAACTTCG[C/G]TGCATCTTCCTGGAT | 9100 |
| rs577488566 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84708543 | CAAACTTTTTATTAG[C/T]TGGAGATTGGTAAGT | 9100 |
| rs577514166 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84702533 | TAATGGCCATTCATT[C/G]ATTCAGCAAATACTG | 9100 |
| rs577515478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84727175 | TGCTTTTTAGTCTCC[C/T]GTGTGAACTGAATTG | 9100 |
| rs577557399 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84741699 | AAAAACACGACTGGA[A/G]TCTTGCCACCAGTTT | 9100 |
| rs577561017 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84763962 | TTGCGATTGGTTGCC[A/G]TGGCTCCTAATGTAG | 9100 |
| rs577577483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84703096 | AAAGTGTTGGTTGAT[C/T]CCTGTTACCTGTATT | 9100 |
| rs577619127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84740438 | GTGGGCAGGCTACCT[A/G]TAAACATTGTTTCCC | 9100 |
| rs577643953 | snp | A/G | 0.000498963 | 0.0157871 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779109 | GCTGTGTGTGCGCCC[A/G]GTGCCCGCTTCGTAG | 9100 |
| rs577645849 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84745738 | TCAACTGGGCTTATA[G/T]ACTGTGGTGTTACCC | 9100 |
| rs577664229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84752220 | TAGGCAGCCCCACCA[A/G]CTCCTGTGACAAAGA | 9100 |
| rs577680755 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84755378 | TAGCTCCTTGCACCC[A/G]TGATCCTGTCTCCTT | 9100 |
| rs577681315 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84740764 | TTGTAAACTAAGGGG[A/C]AGCTGGCATCTGTTG | 9100 |
| rs577716566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84705041 | AGTCTCCTCCCCGTT[A/G]GGCTTGTGTGTACAG | 9100 |
| rs577729771 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84756296 | AAAGGCAGCATGTTA[C/T]TTAACAAAGGTTTCA | 9100 |
| rs577749141 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84748593 | ACAGGCGTGAGCCAC[A/C]GCGCCCAGCTGAGAA | 9100 |
| rs577766127 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84716842 | TCCTGGTCTAAACTT[A/T]TCCCAGCATAATTCA | 9100 |
| rs577779272 | snp | A/G/T | 0.000148887 | 0.00862678 | utr-variant-5-prime, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84700084 | AGTCCCAATGAAACG[A/G/T]GCAGCCATGGCCCTC | 9100 |
| rs577783209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84756027 | CTTCCATTTGGTGGC[C/T]TCAACCCCTGACCTT | 9100 |
| rs577830073 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84707752 | CCACAACTTATAACA[G/T]GTTGTCCAAACAATT | 9100 |
| rs577842036 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84773532 | AGGGGCGCCCTATAC[C/G]TTCCCGTGAAGACTC | 9100 |
| rs577950800 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84735091 | GGAGTGCAGAGTGCA[A/G]TCACAATTCACTGCA | 9100 |
| rs577959924 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84773852 | CTCCAGATCAGCTGT[C/G]TGAGCTGACTTGGAT | 9100 |
| rs577960485 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | USP10 | GRCh38.p7 | 16:84708816 | TTTGTAGAATACTAG[A/G]CACTTTTTTCAGAAC | 9100 |
| rs577990223 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84735520 | CCTCCCATTTCTTTT[C/G]TCTTTCTTTTGTTTT | 9100 |
| rs578034210 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | USP10 | GRCh38.p7 | 16:84725621 | TGTTGGCAGTCTGTT[C/T]TCTGACTCCTGACCT | 9100 |
| rs578063083 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84721644 | GCCATCCTCCTGCCT[C/T]AGCCCTCCCAAGTAA | 9100 |
| rs578133643 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | USP10 | GRCh38.p7 | 16:84761348 | GGTTACATTAATAGG[C/G]GATGTGTTGGGCTCC | 9100 |
| rs578136389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84764855 | AAAGAAAAAGATACA[A/G]GAGAATGTCATCATG | 9100 |
| rs578157084 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84702088 | TGAGACGGGAGTCTT[C/G]CTCTGTCGCCCAGGC | 9100 |
| rs578183104 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84736470 | GAGAAACGAATTCAG[G/T]TGAAAGGTAGCTGGC | 9100 |
| rs578231810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | USP10 | GRCh38.p7 | 16:84726489 | CCTGAGGGCCGTAGT[A/G]GCCTCCACACACCTC | 9100 |
| rs745315503 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84728588 | CCTGCCTCGGCCTCC[C/T]AAAGTGCTGGGATTA | 9100 |
| rs745340564 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84710510 | CAGTGTCCTCAGTGG[C/T]AATTGGATAGAGTAG | 9100 |
| rs745372323 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84762061 | AGTTGTGCTGTGAAG[A/T]ATGAAATATGAACTG | 9100 |
| rs745377080 | snp | C/T | 1.68863e-05 | 0.00290566 | intron-variant | USP10 | GRCh38.p7 | 16:84762957 | TGACAGTGATCAGTT[C/T]ACAGTAACGTGATTA | 9100 |
| rs745388525 | snp | C/T | 3.6001e-05 | 0.00424255 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745545 | AGCCCTCTTCCTCCT[C/T]GCCGGTGGCCTATGT | 9100 |
| rs745394611 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84701072 | ATTAAATATGGGGAA[A/G]TGAAACAAAGTAGCC | 9100 |
| rs745425144 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84754102 | GTCTTTAAGGAGCCT[C/T]CTGTCCAGAGAAGGA | 9100 |
| rs745447135 | snp | A/C | 1.65963e-05 | 0.0028806 | missense, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84733483 | AATCAATTCTTTGTG[A/C]CTCCTCGATCTTCAG | 9100 |
| rs745448247 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84773698 | AATCCCATTTGAGGA[A/C]CAGCAAGAGGAAGAA | 9100 |
| rs745481637 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84747376 | AAAATAAAACACATT[C/T]TTTGGGTGGCAATAG | 9100 |
| rs745488756 | snp | G/T | 3.31214e-05 | 0.00406935 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84772605 | TGCTGCACCTGAAAC[G/T]ATTCGTTTATGAGAA | 9100 |
| rs745544917 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84722065 | ATATATAGAACATTT[C/G]CATTGCTCAGAGAGT | 9100 |
| rs745559524 | snp | A/G | 1.66288e-05 | 0.00288343 | intron-variant | USP10 | GRCh38.p7 | 16:84733543 | AGTCCGTGGGTAGAT[A/G]CAATTAATAGTTATG | 9100 |
| rs745601519 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84716831 | GTGACCGCATGTCCT[C/G]GTCTAAACTTATCCC | 9100 |
| rs745629930 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84777175 | CAGGCGGTTCTCAGC[A/G]CTCCTGTCAGGGGGG | 9100 |
| rs745643000 | snp | A/C | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698755 | TGTGCCACACTACAT[A/C]CCACCAATTTTTGTA | 9100 |
| rs745656947 | snp | A/C/G/T | 0.00116711 | 0.0241309 | utr-variant-5-prime, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84700076 | GATCGCGGAGTCCCA[A/C/G/T]TGAAACGGGCAGCCA | 9100 |
| rs745663557 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84736954 | CCACCTCGCCCGGCT[A/T]ATTTTTTGTGGTTTT | 9100 |
| rs745672228 | snp | A/C/G | 4.992e-05 | 0.00499579 | missense, synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744973 | TTACAGCTATTTGAA[A/C/G]GATGGTGGCGATGAT | 9100 |
| rs745684800 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84770113 | CCGTGTCTCTAAAAC[A/G]TAAGAAGAAATAAAA | 9100 |
| rs745692838 | snp | C/G | 1.68457e-05 | 0.00290216 | intron-variant | USP10 | GRCh38.p7 | 16:84764302 | TAATATTTGCCTTTT[C/G]TAGGGTTTTGCCATG | 9100 |
| rs745708536 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84750146 | GGCACAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 9100 |
| rs745726700 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84761526 | CTTCCAGACTCCTCT[C/G]CCAGTGGGGCCACAA | 9100 |
| rs745745204 | snp | A/G | 0.000167018 | 0.00913679 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745609 | CCTGGTTTCTGAAAA[A/G]CAGGTTGAAGTCAAA | 9100 |
| rs745757021 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84762855 | GGAAACCCATGTCAT[C/G]ATGTCATTGTTTGGA | 9100 |
| rs745772644 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84735835 | TCAAAATCACAGTAA[C/T]CTGCAAAAGGGAAAT | 9100 |
| rs745785536 | snp | C/T | 1.65814e-05 | 0.00287931 | missense, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779042 | CAACTGCTGAACGCA[C/T]AGCCTACCTCCTGTA | 9100 |
| rs745799832 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84717108 | GGGGTGGGCCCTGTG[C/T]GCTGTCTGAGCTCCT | 9100 |
| rs745825960 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84736348 | AGAGCATTCTGCCTT[C/T]CTGCAGAAGCGCCTC | 9100 |
| rs745826112 | snp | A/G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84727966 | CAGGATCCAGTCTAG[A/G/T]GTCAGGAAATGTATT | 9100 |
| rs745841456 | snp | A/G | 1.66793e-05 | 0.0028878 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744888 | AGGCGGAAGTTTTGG[A/G]AAATGATGGTGTCTC | 9100 |
| rs745894961 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84708332 | GCGGGCACCTTTAAT[A/C]CCAGCTGCTCCGAAG | 9100 |
| rs745912383 | in-del | -/GGGTGGGGGTGT | | | intron-variant | USP10 | GRCh38.p7 | 16:84757395 | AGGAGGGAATGAGAG[-/GGGTGGGGGTGT]GTGTGTGTGTGTGTG | 9100 |
| rs745918448 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84772440 | CCACAGGACTCTTGG[A/G]CCTCACCTCTCAGAG | 9100 |
| rs745938519 | snp | A/G | 1.67108e-05 | 0.00289052 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745370 | TCCTCGGGTGAGGGC[A/G]CAGCTACCAACGGGG | 9100 |
| rs745958686 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84706292 | AATTCTAGAGGTTTT[C/T]GAGATTCCTGCCCAA | 9100 |
| rs746014494 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84755097 | GCCTCGTCATAAAGC[A/G]TGTTTTTGAGTCTGT | 9100 |
| rs746027825 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84763900 | CCGTGGATCCAGTGA[C/T]ATTGTGCCTGTTGCG | 9100 |
| rs746034056 | snp | C/T | 0.00241254 | 0.0346475 | intron-variant | USP10 | GRCh38.p7 | 16:84704875 | GGTAAGGTGTTGAGA[C/T]AGAAATGTGGTTTGG | 9100 |
| rs746040891 | snp | C/T | 2.67727e-05 | 0.00365864 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84768289 | CAAGATACGCACAGT[C/T]CAGGATGCACTGGAG | 9100 |
| rs746064074 | snp | C/T | 3.31796e-05 | 0.00407292 | intron-variant | USP10 | GRCh38.p7 | 16:84759866 | TTTAAAACTGCACTA[C/T]TTAACATTTTTTCCC | 9100 |
| rs746066199 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84734899 | TCATTGGGAACTCGG[C/T]CCTTAGCTGTCCTGT | 9100 |
| rs746070279 | in-del | -/GT | | | intron-variant | USP10 | GRCh38.p7 | 16:84735220 | TGTGTGTGTGTGTGT[-/GT]GTGTGTGTGTGTGTG | 9100 |
| rs746081384 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84711505 | ATCGGGAATTCCTGC[G/T]CTCTTTTGCTGTTGT | 9100 |
| rs746103674 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84767412 | GGAAGGGTGGCAGCC[-/T]TTTTTTCCTGGAATG | 9100 |
| rs746106720 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84730409 | TTGAAGGTACATATC[C/T]GTGGAGAAATTATTG | 9100 |
| rs746121877 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84738443 | CTGTCTTCTTTGACC[A/G]CAGAGGGTTTTGAAC | 9100 |
| rs746123493 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84702807 | AGATCAGCCTGACCA[A/G]TATAGTGAGACCCTG | 9100 |
| rs746137308 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84712573 | GGTGTTTCTATAATA[C/G]TTCTAGGCATGAAGT | 9100 |
| rs746143228 | snp | A/G | 1.69628e-05 | 0.00291224 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745311 | CCTGCGTTGGTACCG[A/G]TACTACTGAAAACCT | 9100 |
| rs746168594 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84715031 | CCTCTTGTGCTAAAG[C/T]GATTCTCCTGCCTCA | 9100 |
| rs746232590 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84706830 | CAGGCGTGAGCCACC[A/G]CGCCGGGCCAAGACT | 9100 |
| rs746233664 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84758435 | TGTTAACATTTTTTT[G/T]TTTCTCATTAAAATA | 9100 |
| rs746239040 | snp | A/G | 1.65625e-05 | 0.00287766 | synonymous-codon, nc-transcript-variant, intron-variant | USP10 | GRCh38.p7 | 16:84758753 | AATCCATAAACCAGT[A/G]TCGTTGCAACCCCGT | 9100 |
| rs746242091 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84758447 | TTTGTTTCTCATTAA[A/G]ATAGGTAGTTCTTGT | 9100 |
| rs746261624 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84778382 | CACCATTCTTAATCT[A/G]TTCCACGAAAAAATA | 9100 |
| rs746285028 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84759186 | TCCTTATATGGACAT[C/G]ACAGGACACTTACCC | 9100 |
| rs746300252 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84740639 | ACAGTTCTGAGTGCA[A/G]CAGGTATGTTACTCT | 9100 |
| rs746325844 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84751138 | CCAGTGAGTTGTGTT[A/G]CAGTTGCCTACGGTA | 9100 |
| rs746339856 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84759751 | ATAGAAGAGACTTGA[C/G]TTCACTAGCTGTTAC | 9100 |
| rs746344932 | snp | A/T | 1.66599e-05 | 0.00288611 | intron-variant | USP10 | GRCh38.p7 | 16:84763100 | GAAAGTAGGTTATGG[A/T]CCACTTGCCGCAGAG | 9100 |
| rs746356767 | snp | A/G | 2.5345e-05 | 0.00355976 | intron-variant | USP10 | GRCh38.p7 | 16:84778850 | CCTGTAATGATTCGT[A/G]TGCAGTGCTGTTCTC | 9100 |
| rs746380853 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84751687 | TCTTCCAAATTGATG[G/T]TAATGAGGAAAAGAA | 9100 |
| rs746389809 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84743522 | AACACCGTTCTTTGG[C/G]TATTAGTTTCTTTTC | 9100 |
| rs746399587 | snp | C/G | 1.65795e-05 | 0.00287914 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744708 | TGCCGAGAACCCCCA[C/G]CTACAGTATTTCAAG | 9100 |
| rs746428925 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84707701 | GATTGAAGTGACTTA[C/T]CAGGATCCAGTGTGC | 9100 |
| rs746432869 | snp | C/T | 2.46624e-05 | 0.0035115 | intron-variant | USP10 | GRCh38.p7 | 16:84764061 | TGTCGTAAATAGTAG[C/T]GTAAGCAGATGCTCT | 9100 |
| rs746444939 | snp | C/T | | | missense, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779062 | TACCTCCTGTATTAC[C/T]GCCGAGTGGACCTGC | 9100 |
| rs746478511 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84743115 | TGGAACCAAAATGAA[C/G]AGCCAGCCCCTACAT | 9100 |
| rs746515294 | snp | C/T | 1.65605e-05 | 0.0028775 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84772597 | TGTCCTCGTGCTGCA[C/T]CTGAAACGATTCGTT | 9100 |
| rs746521926 | snp | C/G | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698467 | CAACAAATAGTAAAA[C/G]CAGCTTAAAAGACAT | 9100 |
| rs746522487 | snp | A/G | 1.65987e-05 | 0.00288082 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84733473 | TGATGAATTCAATCA[A/G]TTCTTTGTGACTCCT | 9100 |
| rs746526430 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84769854 | GGTGGCGGTGTGGGG[G/T]CAGGGGTTGAGGCGC | 9100 |
| rs746530557 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84709267 | TGAAGTCAGAGAACC[A/G]TTCCCGTGGAAGTGA | 9100 |
| rs746581197 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84735738 | CTTCAGAACTCGTAG[C/T]GTGTGTGGGCTTATT | 9100 |
| rs746583609 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84761357 | AATAGGGGATGTGTT[A/G]GGCTCCCCAAGACCA | 9100 |
| rs746598927 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84725859 | AAACAGTCTATTGCT[C/G]TTTTCATGTTTCCCC | 9100 |
| rs746616827 | snp | C/T | 6.6324e-05 | 0.00575826 | intron-variant | USP10 | GRCh38.p7 | 16:84758829 | TTCCTGGACGCCGTC[C/T]GCAAGGCCAGCTTGT | 9100 |
| rs746627408 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84753123 | AGGCAGGCACCACCA[C/T]GTACAGCTAATTTTT | 9100 |
| rs746632765 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745082 | TTTATGGGTGACATG[C/T]CCCCGTCAGTTACGC | 9100 |
| rs746644024 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84746531 | CACAGTGCTAAGTAT[C/T]TGTGTGCCTGAACAC | 9100 |
| rs746668656 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84728464 | CCTGCCTCAGCCTCC[C/T]GGGTAGCTGGGACTA | 9100 |
| rs746688864 | snp | C/T | 1.67624e-05 | 0.00289498 | intron-variant | USP10 | GRCh38.p7 | 16:84733395 | AAAGTATATAATTTG[C/T]ATATTTTATGTGATC | 9100 |
| rs746716348 | snp | C/T | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699558 | ACAAATGAATGAATG[C/T]GCGGCAACGGGATCT | 9100 |
| rs746788125 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84775541 | CCGGCTGTGCTTGTG[C/G]CACCTGTGGGTGACA | 9100 |
| rs746811908 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84776435 | TTTTCTCCCCCCGAT[C/T]ACAATTCCTCCTCAA | 9100 |
| rs746816870 | snp | C/T | 1.84882e-05 | 0.00304036 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745594 | TCCCGCCATATCTCC[C/T]CTGGTTTCTGAAAAG | 9100 |
| rs746833270 | snp | G/T | 1.65737e-05 | 0.00287864 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779031 | GGTGGTGAAACCAAC[G/T]GCTGAACGCACAGCC | 9100 |
| rs746879114 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84749596 | AAAAAAAATTATACA[C/T]ACACAAAATGCTTGG | 9100 |
| rs746883009 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84776696 | GGGCTAGGGATTGCT[C/T]CTCTCCTGGTCAGGG | 9100 |
| rs746885194 | snp | C/T | 7.88861e-05 | 0.00627988 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84760250 | ACAGACTCCTGACAG[C/T]TAACAAGTCAAGCCT | 9100 |
| rs746899891 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84741510 | TTCCCATGCACATCA[C/G]TTCTTTGAGTTCACC | 9100 |
| rs746907157 | in-del | -/GGGGGTGTGT | | | intron-variant | USP10 | GRCh38.p7 | 16:84757399 | GGGAATGAGAGGGGT[-/GGGGGTGTGT]GTGTGTGTGTGTGTG | 9100 |
| rs746917892 | in-del | -/C | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698061 | CACGTCCCCCAGTTT[-/C]TATCCAAGTGCAGAT | 9100 |
| rs746955508 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84734933 | CCCCGTTGGGCAGTG[C/T]ATCTCCCCTGGTTCC | 9100 |
| rs746956833 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84716782 | TGAAGAGTGAAGATT[C/T]TACCTTTATATACAC | 9100 |
| rs746957188 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84741879 | GCTGATGGCAGGATC[A/C]ATTTCTCTGTGTCTG | 9100 |
| rs747000715 | snp | A/C | 1.78245e-05 | 0.00298529 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745539 | ATTCTAAGCCCTCTT[A/C]CTCCTCGCCGGTGGC | 9100 |
| rs747003403 | in-del | -/A | | | intron-variant | USP10 | GRCh38.p7 | 16:84716892 | CTGAGATATGCCTCT[-/A]ATTTGGATGATAAAT | 9100 |
| rs747049902 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84706224 | CTTTTTACTTTTGAT[A/G]GGACATGTTGAAGTT | 9100 |
| rs747050810 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84759174 | CTGCTTCGTAGATCC[A/T]TATATGGACATCACA | 9100 |
| rs747059839 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84778251 | AGTCCCAGGGTCCCT[C/T]CTGCCATGTGGGCCG | 9100 |
| rs747067383 | snp | C/T | 1.73697e-05 | 0.00294696 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745231 | CCCCGGGGCTGATTT[C/T]GGTCAGTCCTGCTTC | 9100 |
| rs747092400 | snp | G/T | 1.66164e-05 | 0.00288235 | intron-variant | USP10 | GRCh38.p7 | 16:84759853 | AAAGTATATATTGTT[G/T]AAAACTGCACTATTT | 9100 |
| rs747108118 | in-del | -/TAGT | 2.9804e-05 | 0.0038602 | intron-variant | USP10 | GRCh38.p7 | 16:84745676 | TAAAGATTGCAGGTA[-/TAGT]TAGTTGAAAAGATAC | 9100 |
| rs747108897 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84721822 | CCTGCCTCAGCCTCT[C/T]GAGTAGCTGGGACTA | 9100 |
| rs747152293 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84742909 | GATTGAGAATTGAGA[C/T]GTGTACAGCACATCT | 9100 |
| rs747186966 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84772385 | GGAGCATTGGTAGAT[A/C]TCAGAGCTTCTGTGG | 9100 |
| rs747187401 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717788 | GCCTTTGATTCATTG[A/C]GGTCCTAGTCTCTGG | 9100 |
| rs747201998 | in-del | -/GA | | | intron-variant | USP10 | GRCh38.p7 | 16:84734896 | ATTCATTGGGAACTC[-/GA]GGCCCTTAGCTGTCC | 9100 |
| rs747204763 | snp | A/C | 1.65864e-05 | 0.00287974 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764210 | GACTTCCGTCACCCG[A/C]CAGGCGGATTTTGTT | 9100 |
| rs747216657 | snp | C/G | 2.15459e-05 | 0.00328215 | utr-variant-5-prime, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84700054 | GAAGCAGCGTGAGCA[C/G]CCGGAGGATCGCGGA | 9100 |
| rs747217081 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84726157 | TTTGGAACAACCTGC[A/G]TATTTATTCAAATTT | 9100 |
| rs747239100 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84710773 | TACCAGAATCACCTG[A/G]CACCCTGGGTGCCAC | 9100 |
| rs747243892 | in-del | -/TTTT | | | intron-variant | USP10 | GRCh38.p7 | 16:84734654 | TGTCAACTGAATTGA[-/TTTT]TTTTTCCTTATAGTT | 9100 |
| rs747252915 | in-del | -/C | 2.80911e-05 | 0.00374763 | intron-variant | USP10 | GRCh38.p7 | 16:84768370 | AGAGGTATGTTCACA[-/C]TTGATTTTGAACCTT | 9100 |
| rs747283732 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84721311 | TACTGAAGAATTCTT[A/C]TTCCGTAGATGAGAG | 9100 |
| rs747294542 | snp | G/T | 1.68009e-05 | 0.00289831 | intron-variant | USP10 | GRCh38.p7 | 16:84764294 | GAATAACTTAATATT[G/T]GCCTTTTCTAGGGTT | 9100 |
| rs747312596 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84756035 | TGGTGGCTTCAACCC[C/G]TGACCTTCCCAGAGT | 9100 |
| rs747319866 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84713235 | GCCAGGCATTGTTGG[C/T]ACAGAAATGGAGGGG | 9100 |
| rs747328650 | snp | C/G | 1.72698e-05 | 0.00293847 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744648 | GACAAGAATATCAGA[C/G]AATTGAGTTTGGTGT | 9100 |
| rs747337189 | snp | C/G | 1.66067e-05 | 0.00288151 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84763080 | AGCTTCTCTCACCAA[C/G]TAATGAAAGTAGGTT | 9100 |
| rs747370223 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84765114 | CATGTGTTTTGGTAA[A/G]AGAAGACAGTGTATC | 9100 |
| rs747428192 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84747200 | GTGACCAGATCTTCA[C/G]ATTGTCACCCTAGTA | 9100 |
| rs747473152 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84754387 | AAAAGGTTTATTCTG[C/T]GTTTAACGACGTCGT | 9100 |
| rs747483559 | snp | C/T | 1.65905e-05 | 0.0028801 | intron-variant | USP10 | GRCh38.p7 | 16:84775138 | TAAAAGTGCTTCAAG[C/T]CATTGATATTTTGTT | 9100 |
| rs747486817 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84732343 | CCAGTACTGATCATA[C/T]GTGGGCATTTGTAGG | 9100 |
| rs747505610 | snp | G/T | 0.00010247 | 0.00715711 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745302 | GGGCTCAGCCCTGCG[G/T]TGGTACCGATACTAC | 9100 |
| rs747507455 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84758383 | TTTAAGGAAGAAAGG[C/G]TGTATCTCTCAAATC | 9100 |
| rs747519866 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84740035 | ATTGTAGCTGATTTA[C/T]ATGTCCATTGGAGTT | 9100 |
| rs747565532 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84704977 | TGGAGTGCGGGCCCA[A/G]CACCTGCTACCGTCT | 9100 |
| rs747570883 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84732862 | CACATTCTGAATTCC[A/G]TGAAATCAGGCTTGC | 9100 |
| rs747597707 | snp | C/G | 1.65679e-05 | 0.00287814 | missense, intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84740366 | GTGGATAAACTACCT[C/G]ATGGTAAGCTAGTTC | 9100 |
| rs747605260 | snp | A/T | | | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84715935 | CACAGCCTCCGTCAC[A/T]CCAGCCTGACCAAGA | 9100 |
| rs747666006 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84775401 | ACTCTGCGTAGATGA[C/T]GGATTATCATCTTGG | 9100 |
| rs747669577 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84715065 | TCCTGAGTAGCTGGG[A/G]CTACAGGCATGCACC | 9100 |
| rs747704226 | snp | A/G | 3.64451e-05 | 0.00426863 | intron-variant | USP10 | GRCh38.p7 | 16:84745690 | TATAGTTGAAAAGAT[A/G]CAAATCTAGAGTGAA | 9100 |
| rs747777954 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84735649 | GAAATGGATGAAAAG[A/G]GTACAGATGGTAAGT | 9100 |
| rs747789445 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84751986 | TTCAGTGGGCTGATT[G/T]GTGGCAGCCCTTGTG | 9100 |
| rs747839614 | snp | A/G | 3.32624e-05 | 0.004078 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744983 | TTGAAAGATGGTGGC[A/G]ATGATAGTATCTCCA | 9100 |
| rs747887250 | snp | C/T | 9.94547e-05 | 0.00705106 | intron-variant | USP10 | GRCh38.p7 | 16:84758709 | ATATGCTTCTTCACT[C/T]TTTCAGAGTTGCTGG | 9100 |
| rs747914919 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84704028 | AGGATTACGAAGCTT[A/T]ATGATTGCTGTTTAA | 9100 |
| rs747929630 | snp | C/T | 1.67787e-05 | 0.00289639 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745440 | CCAAACCCGAGAGTG[C/T]ATCACCTCCTGCTGA | 9100 |
| rs747981796 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84702506 | CCTACTGTCCTAAGA[C/G]TCTTGCAGCCTTAAT | 9100 |
| rs747993543 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84754915 | GGAATCCAAGGCAGG[C/T]GGATTGCTTGAGGCC | 9100 |
| rs747995261 | snp | C/G | 3.31658e-05 | 0.00407208 | intron-variant | USP10 | GRCh38.p7 | 16:84772503 | AGCTGTTGCAAGTAA[C/G]ACAGGGACGGTGTGT | 9100 |
| rs748002946 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84737515 | TGTGCCTGTGGAATA[A/C]AACACACACATTTCC | 9100 |
| rs748006248 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84769475 | GAAACTTGGTAGTTG[A/G]CTTCAGTGAATGAGC | 9100 |
| rs748028323 | snp | C/T | 1.67728e-05 | 0.00289588 | intron-variant | USP10 | GRCh38.p7 | 16:84733388 | TTTTCTGAAAGTATA[C/T]AATTTGTATATTTTA | 9100 |
| rs748033645 | snp | A/G | 3.31422e-05 | 0.00407063 | intron-variant | USP10 | GRCh38.p7 | 16:84759978 | TTTGTTGATGCTATT[A/G]CATATTGGGAGTTAT | 9100 |
| rs748052407 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84740951 | GCTTAAGTACCCAGC[A/G]TTGGAATACCAACAA | 9100 |
| rs748078017 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84732337 | TTATACCCAGTACTG[A/C]TCATACGTGGGCATT | 9100 |
| rs748097284 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84722299 | GTACTGGGTAGTATT[C/G]CTTTGTGGATGTCCC | 9100 |
| rs748108198 | in-del | -/TAG | | | intron-variant | USP10 | GRCh38.p7 | 16:84708122 | AGACTTCCACCCCCT[-/TAG]TAGTAGTCATGCTGT | 9100 |
| rs748116208 | snp | C/T | 1.66103e-05 | 0.00288182 | missense, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84733456 | TTTGGAGATTTTAGC[C/T]CTGATGAATTCAATC | 9100 |
| rs748129616 | snp | A/G | 6.1237e-05 | 0.00553306 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84760177 | TCCATTGCAGCTCTT[A/G]GAGATAAAATCGTGA | 9100 |
| rs748131979 | in-del | -/A | 1.65853e-05 | 0.00287964 | intron-variant | USP10 | GRCh38.p7 | 16:84775145 | CTTCAAGCCATTGAT[-/A]ATTTTGTTTTCCAGA | 9100 |
| rs748173592 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84732273 | CCCTGGAAGCTACTA[C/G]ACTGTTTAGTTCCAT | 9100 |
| rs748211770 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84777204 | GGCTTGCAGGTGTGA[A/G]TGACACACGGCTCAG | 9100 |
| rs748214853 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84704337 | GAATTTGTAATTAGG[A/C]TGTTACTTTTCTATT | 9100 |
| rs748305706 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84724758 | CAAAGTTTTACTCTC[A/G]TAGTCTCGCATAGTT | 9100 |
| rs748307642 | snp | C/T | 3.46218e-05 | 0.0041605 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745510 | GCCCAAGTCCTGGGC[C/T]AGCCTCTTTCATGAT | 9100 |
| rs748320734 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84770276 | GATTTGGGACAGCTT[A/G]TATGGAAGTATCTAT | 9100 |
| rs748331973 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84750219 | TCAAGACCAGCCTGG[C/T]CAACATAGGGAAATC | 9100 |
| rs748339532 | snp | C/T | 4.97484e-05 | 0.00498715 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744757 | CCCTGAATTTATTCT[C/T]GGTTGTACAGCTTCC | 9100 |
| rs748347117 | snp | C/T | 8.37528e-05 | 0.00647066 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84778956 | AGACGTCTTCCAGAT[C/T]GGTCTGAATGGCTGG | 9100 |
| rs748350801 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717201 | GGGAGCTTCAGAGGG[C/T]CTGTGAAGTTCTGAA | 9100 |
| rs748386969 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84742731 | CACATGGCGTCCATT[A/G]TGAGTGTTCCTCCAT | 9100 |
| rs748424224 | snp | C/G | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698104 | TGGTTAAAATTATAG[C/G]ACAGACACTATATTG | 9100 |
| rs748433546 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84725546 | GCTGAGATTAGAGGC[A/G]CCTGCCACCATGCCC | 9100 |
| rs748435063 | snp | C/T | 0.00141134 | 0.0265269 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764150 | GCAGGAAGAACAAGG[C/T]GAAGGAAGCGAGGAT | 9100 |
| rs748437426 | snp | A/G | 1.65729e-05 | 0.00287857 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779019 | CAACCAGTACCAGGT[A/G]GTGAAACCAACTGCT | 9100 |
| rs748444540 | snp | A/T | | | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719619 | GATTGGTTACCTGCT[A/T]TTATGTGGAAAATAG | 9100 |
| rs748444800 | snp | C/G | 1.71413e-05 | 0.00292752 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745295 | ACAGCTGGGGCTCAG[C/G]CCTGCGTTGGTACCG | 9100 |
| rs748533348 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84709201 | ATAATCACAGTTACG[G/T]ACACGTCACTCCAAA | 9100 |
| rs748541465 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84774004 | CCTGTAATCCCAGCA[C/G]TTTGGGAGGCCGAGG | 9100 |
| rs748551307 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84753776 | CCAACAACTTTAATC[C/T]CCAGATGTTTAATTG | 9100 |
| rs748637625 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84738637 | TCTTCTGGGTGTCAA[C/T]GTGATGCGTACTAGG | 9100 |
| rs748660779 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84746303 | GTTACAGTAGGAAGT[C/T]AGAAATGCAGCAGGG | 9100 |
| rs748667344 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84715637 | TTAGGGTGCCCTCCC[-/T]TTTTTTTTTTAAAAA | 9100 |
| rs748688864 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84731527 | TTTCCTCCCCCCAAG[A/G]AAAAGGTGTATGTGA | 9100 |
| rs748730200 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84713091 | CAATTATGTGTCACC[A/G]GTGAACATGGAAAGA | 9100 |
| rs748754365 | snp | A/G | 1.65608e-05 | 0.00287752 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84772614 | TGAAACGATTCGTTT[A/G]TGAGAAGACTGGTGG | 9100 |
| rs748819894 | snp | C/G | 1.66955e-05 | 0.0028892 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744901 | GGAAAATGATGGTGT[C/G]TCAGGTGGTCTTGGA | 9100 |
| rs748855289 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84740086 | TCATTTTCGGATCTG[C/T]TTAATAGTGATAAAT | 9100 |
| rs748885722 | snp | A/G | 1.65663e-05 | 0.002878 | synonymous-codon, intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84740359 | ACAGGCTGTGGATAA[A/G]CTACCTGATGGTAAG | 9100 |
| rs748905618 | snp | A/C | 1.68063e-05 | 0.00289877 | intron-variant | USP10 | GRCh38.p7 | 16:84759344 | ATTTCCTTTACGCTT[A/C]CTTACTGCCACTACA | 9100 |
| rs748943886 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84715117 | TATTTTTTAGTAGAG[A/T]TGGGGTTTCACCATA | 9100 |
| rs748990938 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84715822 | TTTTTTCACTTTTCA[C/T]TTCTTCATCTTTTCA | 9100 |
| rs748995383 | snp | C/T | 1.91305e-05 | 0.00309272 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745631 | GAAGTCAAAGAAGGG[C/T]TTGTTCCGGTTTCAG | 9100 |
| rs749014177 | snp | C/G | 1.65888e-05 | 0.00287996 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84763072 | CCTAAAGAAGCTTCT[C/G]TCACCAAGTAATGAA | 9100 |
| rs749035076 | in-del | -/CAG | 3.32662e-05 | 0.00407824 | cds-indel, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745029 | ATGGCCATGCCAATT[-/CAG]CAGTCCCGAACAGTG | 9100 |
| rs749046387 | in-del | -/AG | | | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719893 | ACTGAGACAGCAAAC[-/AG]TGGATTCCTTCCTTA | 9100 |
| rs749090097 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84761549 | GGCCACAAGGCTACG[C/T]GTAACTACTCCAGCA | 9100 |
| rs749090330 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84702686 | TAATGGGAGGTGGAA[A/C]AAGTTACAGTTTAAA | 9100 |
| rs749111440 | snp | A/C | 1.65696e-05 | 0.00287828 | intron-variant | USP10 | GRCh38.p7 | 16:84759960 | AGGTTAGTAAAAATG[A/C]GTTTTGTTGATGCTA | 9100 |
| rs749150549 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84743356 | TCTAAAGCATACGAA[C/G]ATTCAGGAGGCCTCG | 9100 |
| rs749174288 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84736409 | TTTGCTTGCTTGGCA[C/G]CTTGCCACTGGCAAG | 9100 |
| rs749185100 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84728608 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGTGTC | 9100 |
| rs749188954 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84747421 | ATGTATATATATTTT[G/T]AAGAGTATTTTATTC | 9100 |
| rs749189043 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84728972 | CCTGGCTAATTTTTG[-/T]ATTTTTAGTGGAGGT | 9100 |
| rs749195522 | snp | G/T | 9.44689e-05 | 0.00687208 | intron-variant | USP10 | GRCh38.p7 | 16:84768146 | TCTTAAGGGAAAGTG[G/T]CAAGGAGTGGTCTCT | 9100 |
| rs749197847 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84754236 | ATTTAGGATCATTAT[A/G]AGAGATTAATAACAG | 9100 |
| rs749215411 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84729379 | GTGATATCGATGACT[C/T]GTCTTTTACTGACAT | 9100 |
| rs749277198 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84701370 | TTTTGTAAGTAGTGT[A/C]GGTCTTTGCGCCAAA | 9100 |
| rs749279273 | snp | A/C | 4.89237e-05 | 0.00494565 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84768324 | TGGTGGCAAGAGAAT[A/C]TGTCCAAGGTTATAC | 9100 |
| rs749331750 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84713039 | TGTCCCCCAAATGCA[A/G]GAACCATGGAGCAGC | 9100 |
| rs749343299 | snp | C/G | 2.12181e-05 | 0.00325709 | intron-variant | USP10 | GRCh38.p7 | 16:84764073 | TAGTGTAAGCAGATG[C/G]TCTCCTTTTCAGAAC | 9100 |
| rs749366307 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84769061 | TCTTCTCTGTTATAT[A/C]TCTTAGGTTGTGGCA | 9100 |
| rs749376494 | snp | A/C/T | 3.31649e-05 | 0.00407204 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744734 | TCAAGCACACTGAAC[A/C/T]CTCAGGCCCCTGAAT | 9100 |
| rs749378981 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84752345 | GAAAGTTTGTTATTA[G/T]AGCCAACTTCTATTA | 9100 |
| rs749380562 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84703664 | TTTCCTTTGCATAGT[A/G]ACAGCAAGCTATTTA | 9100 |
| rs749392992 | in-del | -/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84770770 | GAGCGAGACTCCGTC[-/C]CCAAAAAAAAAAAAA | 9100 |
| rs749395865 | snp | A/G | 1.69043e-05 | 0.00290721 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84778941 | CGGCCATTACACTAC[A/G]GACGTCTTCCAGATC | 9100 |
| rs749396198 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84738517 | GCCCTTATAGACCCA[C/T]CTCTCTGCTCCAGGT | 9100 |
| rs749420109 | snp | C/G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84764993 | CTTGCAACATAAAAC[C/G/T]ACCTCCGGGAGGCAG | 9100 |
| rs749420989 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84749119 | ACATTGAATAACCCT[C/T]GGGATCATATAGGGC | 9100 |
| rs749451636 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84731380 | TGATATTAAACAAAA[C/T]AGCATGATTTTAGTT | 9100 |
| rs749477595 | snp | A/C | 3.33934e-05 | 0.00408603 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745378 | TGAGGGCACAGCTAC[A/C]AACGGGGTGGAGTTG | 9100 |
| rs749511016 | snp | A/C | 3.34253e-05 | 0.00408797 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745428 | ACTTGGACCCAACCA[A/C]ACCCGAGAGTGCATC | 9100 |
| rs749540543 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84723778 | ATTTAAAGTGTATAT[G/T]TCCATGAATTTTAAC | 9100 |
| rs749557169 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84732085 | TTAATGTATATTTAT[A/G]GTTTTGGTAGATGTT | 9100 |
| rs749576805 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84704195 | TTTAAAGATATAATT[G/T]CAGACATGTAGGTAC | 9100 |
| rs749602667 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84759796 | AAAATCTACTATACT[C/T]GTATAGCTGATATTC | 9100 |
| rs749648720 | snp | C/T | 1.71655e-05 | 0.00292958 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745165 | GCCTGACAGTCCTTT[C/T]CCCGGAGCACTCGGC | 9100 |
| rs749648744 | snp | C/T | 1.65743e-05 | 0.00287869 | missense, nc-transcript-variant, intron-variant | USP10 | GRCh38.p7 | 16:84759391 | TGGTTGCTTGCCCGC[C/T]GATGTACCACCTGAT | 9100 |
| rs749672013 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84742969 | GCTGAATGACACAAC[A/G]CGTTCTAGTTTCTAA | 9100 |
| rs749673726 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84724025 | TTGGTGGAATCTTGA[A/C]CTTCTACTAGGGCTA | 9100 |
| rs749697255 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779857 | GTCCCTAATTGTACA[C/T]AGTTTAGTGATATCT | 9100 |
| rs749725101 | in-del | -/CTGTGTGCG | 1.6851e-05 | 0.00290263 | cds-indel, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779086 | GACCTGCTGTAAACC[-/CTGTGTGCG]CTGTGTGTGCGCCCA | 9100 |
| rs749743865 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718789 | TTTTTCTTCTTTTAG[A/T]TTTGTTGTTGTTGTT | 9100 |
| rs749760650 | snp | C/G | 1.6615e-05 | 0.00288223 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764136 | GTCAATGAAGAAGAG[C/G]AGGAAGAACAAGGTG | 9100 |
| rs749761889 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84752431 | GGTCAAGTTTCAACC[C/T]AGAAGTTGCCTGCCC | 9100 |
| rs749783745 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84726957 | GCAGAGTTGCTGAAA[C/G]CTTAGGGGGCTTCCC | 9100 |
| rs749796171 | in-del | -/T/TT | | | intron-variant | USP10 | GRCh38.p7 | 16:84701934 | CTCATAATTTTCTTC[-/T/TT]TTCTTTTTTTTTTTT | 9100 |
| rs749799104 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84708804 | GTTTAGAATTAATTT[G/T]TAGAATACTAGACAC | 9100 |
| rs749818045 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84737655 | AGTTTGCTGGTGGTC[A/G]TCTCACCAGATCCCT | 9100 |
| rs749839147 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84743833 | GCTTCCCAAGAGATA[C/T]TTAAAAGTTCACAAT | 9100 |
| rs749910061 | snp | A/C/G | 5.0585e-05 | 0.00502895 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745328 | ACTACTGAAAACCTT[A/C/G]GAGTTGCTAATGGAC | 9100 |
| rs749942562 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84711181 | ATTATGCCTTTTAAG[C/T]AAGCATTTACCCAGT | 9100 |
| rs749953904 | snp | C/T | 6.62669e-05 | 0.00575578 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84775192 | GTTAAAAATAAGAAT[C/T]TTAAATGCCACCGAA | 9100 |
| rs749994263 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84754733 | CTGTCTCACAAATAA[A/C]TGCTGGGAAAAAAGT | 9100 |
| rs749995784 | snp | G/T | 1.65743e-05 | 0.00287869 | intron-variant | USP10 | GRCh38.p7 | 16:84744603 | GTTTGTAGAACTGGG[G/T]TCTTAACTAATAGTT | 9100 |
| rs750020049 | snp | A/T | 1.6804e-05 | 0.00289858 | intron-variant | USP10 | GRCh38.p7 | 16:84759510 | TGTTAAGTGGTGGGG[A/T]TTTTCCCGTCTGATA | 9100 |
| rs750042145 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84763537 | TAAAGCATCTCCTGC[A/G]TAACCACAGTCCCTT | 9100 |
| rs750090361 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84748364 | GCCGGAATGCAGTGG[C/T]GCAATCTCGGCTCAC | 9100 |
| rs750106438 | snp | G/T | 1.7172e-05 | 0.00293013 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745287 | TGTCAAGGACAGCTG[G/T]GGCTCAGCCCTGCGT | 9100 |
| rs750130516 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84732579 | AGCCTCCCGAGCAGC[C/G]GGGACTACAGGTACA | 9100 |
| rs750158272 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84704572 | TGACCATTTCTGTCA[A/G]TACAGGCTGGATGAA | 9100 |
| rs750207084 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84704635 | GGGTATGTGTATAGT[A/G]TTTGTTTCAAGGATC | 9100 |
| rs750235512 | snp | C/T | 1.8265e-05 | 0.00302195 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779130 | CGCTTCGTAGGACAC[C/T]ACCTCACACTCACTT | 9100 |
| rs750248732 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84753162 | TATTTTTTATTTTTC[A/G]TAGCAACAGAGTCTC | 9100 |
| rs750263032 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84711759 | CTGAGATGGAGTCTT[C/G]TTCTGTCACCCAGGC | 9100 |
| rs750270469 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84777911 | AATGCTGCCGGACAG[C/T]CGCCTTCCCGAGGCT | 9100 |
| rs750321980 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84771352 | AGTCTAGGAGTTCAA[C/G]ACCAGCTGGGCTCAT | 9100 |
| rs750334174 | snp | G/T | 1.65718e-05 | 0.00287848 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84763042 | TCTAAATGGACTTCA[G/T]GAGGAAATGTTGAAC | 9100 |
| rs750344954 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84750850 | CTCTGAAAACATTGC[A/G]TTGAGGTATCTAGCA | 9100 |
| rs750371476 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84733407 | TTGTATATTTTATGT[G/T]ATCAGTGACTCTCTT | 9100 |
| rs750384776 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84751464 | TCATGCGGCGTGATC[C/T]AAGTTAAAAAGGCGT | 9100 |
| rs750397848 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84743308 | GGATTGTGCTGCCAC[C/T]ACCCTTCACCCCCCA | 9100 |
| rs750404703 | in-del | -/TA | | | intron-variant | USP10 | GRCh38.p7 | 16:84727387 | GAGGAGAGAAAACAC[-/TA]TAAACAGTCAAACAT | 9100 |
| rs750414301 | snp | A/G | 2.51348e-05 | 0.00354496 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745661 | GAGGATCCTGTAGCC[A/G]TAAAGATTGCAGGTA | 9100 |
| rs750414870 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84726823 | TTTGCTCCCCCGAAT[C/G]GCAGGCATTTCTGTG | 9100 |
| rs750422107 | snp | A/T | 1.67066e-05 | 0.00289016 | intron-variant | USP10 | GRCh38.p7 | 16:84763119 | CTTGCCGCAGAGTTG[A/T]GCAAGAGTTCGCTGT | 9100 |
| rs750424424 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84725976 | CATTTGCCACTGTGA[C/G]GCTTAGCTGTGCATC | 9100 |
| rs750437032 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84708138 | AGTAGTAGTCATGCT[A/G]TCCGGTGTTCATAGT | 9100 |
| rs750461056 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84735362 | GGTGGGTACCTGTTT[G/T]CAAGTGAGTAGACAA | 9100 |
| rs750462036 | snp | C/T | 1.65614e-05 | 0.00287757 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84772552 | TTAGGTTGAGATAAG[C/T]CGAAGAGTGACTCTG | 9100 |
| rs750482421 | snp | C/T | 1.66599e-05 | 0.00288611 | intron-variant | USP10 | GRCh38.p7 | 16:84733422 | GATCAGTGACTCTCT[C/T]ATTTTTTTTCAGTAT | 9100 |
| rs750513545 | snp | A/G | 7.27379e-05 | 0.00603023 | intron-variant | USP10 | GRCh38.p7 | 16:84760144 | GTTCATTGTAGTTAG[A/G]AAAACCTGTGTCCTC | 9100 |
| rs750520954 | snp | C/G | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698034 | GACAACCATAAATCA[C/G]TAGTGAGTTTTCACG | 9100 |
| rs750540047 | in-del | -/TTT | | | intron-variant | USP10 | GRCh38.p7 | 16:84725294 | GAATGGAAGAAACAA[-/TTT]ATGGCTCTTTGTGTG | 9100 |
| rs750542956 | snp | A/G | 1.66549e-05 | 0.00288568 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84745049 | GTCCCGAACAGTGTC[A/G]GTGCAGAGGATGCAG | 9100 |
| rs750580567 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84773848 | TCGCCTCCAGATCAG[C/T]TGTCTGAGCTGACTT | 9100 |
| rs750592636 | in-del | -/AACTA | | | intron-variant | USP10 | GRCh38.p7 | 16:84772888 | AATAGAGGCAAAAAT[-/AACTA]AACTCTATAATCTTA | 9100 |
| rs750626065 | snp | C/T | | | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744944 | AAAAAGAAGAAAAAG[C/T]GGCCACCTGGATATT | 9100 |
| rs750642980 | in-del | -/C | 0.00143401 | 0.0267385 | intron-variant | USP10 | GRCh38.p7 | 16:84772728 | TCGTGGTGACACACT[-/C]CTGCACATCAGAAGC | 9100 |
| rs750650984 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84752756 | AAGAAGAGGAGCTCA[C/T]GAACTTCATAAAGCG | 9100 |
| rs750655842 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84727617 | CATTTGCTTAATCAT[G/T]TGTGTGTGCTGGAAT | 9100 |
| rs750660432 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84710003 | AGGCCGGGTGCGAGG[C/T]TCACGCCTGTAATCC | 9100 |
| rs750678497 | snp | C/T | 1.69573e-05 | 0.00291177 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745128 | GCCCCCAGAACTCCA[C/T]AGACTCTGTCAGTGA | 9100 |
| rs750709257 | snp | G/T | 3.53951e-05 | 0.0042067 | intron-variant | USP10 | GRCh38.p7 | 16:84768397 | CCTTTCTACTAAGGT[G/T]CTCTGGTTTGGTGGA | 9100 |
| rs750722268 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84720186 | AAAATCATTTCTGTA[C/G]CTAGGTTCTTTTTTC | 9100 |
| rs750749860 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84722652 | CTGAAACCTTCACCT[C/G]CCAGGTTTAAGCAGT | 9100 |
| rs750764597 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84776370 | ACACTGCAAGGTGCC[A/G]GGCTTCCCTCTCTTC | 9100 |
| rs750769183 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84730860 | AAAATACCTGATAAT[C/G]CTGCAGAACATTCTG | 9100 |
| rs750786007 | snp | A/C | 1.65872e-05 | 0.00287981 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744786 | CCAAAATAACCCCTG[A/C]TGGTATCACTAAAGA | 9100 |
| rs750855776 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84748816 | GAAGTAGCTTTGTCA[A/G]ACACTGAAAGTAAGG | 9100 |
| rs750949071 | snp | G/T | | | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84716481 | GGACGAAATACAGAC[G/T]GACACAAGGAGATAA | 9100 |
| rs750982813 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84760427 | TTGGATGATATGGTG[C/T]ACCAAGCACTGCTCT | 9100 |
| rs750997559 | snp | C/T | 1.7086e-05 | 0.00292279 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745480 | CTCTGCATCAGGCAC[C/T]CTTCCTGTCAGCCAG | 9100 |
| rs751011593 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84761867 | AGCCACCCAGGCCTG[C/T]TATGAAAAGTCTTCA | 9100 |
| rs751020306 | snp | G/T | 1.74482e-05 | 0.00295361 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745212 | CAGGGCAGCCAGAGG[G/T]GGGCCCCGGGGCTGA | 9100 |
| rs751024840 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84725124 | TTTTGCAGCTAACAC[C/T]GTAGTCCATTTTAGA | 9100 |
| rs751033045 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717443 | CCTTCCCTGACCCCA[C/G]TTCTTTGAAGGCAGG | 9100 |
| rs751054560 | snp | A/G | 1.66729e-05 | 0.00288724 | intron-variant | USP10 | GRCh38.p7 | 16:84759492 | GTAAGGTGGTGAAAG[A/G]TGTGTTAAGTGGTGG | 9100 |
| rs751064200 | in-del | -/CAA | | | intron-variant | USP10 | GRCh38.p7 | 16:84755795 | AGAGTGAGACTGTCT[-/CAA]AAAAAAAAAAAAAAA | 9100 |
| rs751067602 | in-del | -/C | 0.00130634 | 0.0255237 | intron-variant | USP10 | GRCh38.p7 | 16:84732459 | CTTTTTTTTTTTTTT[-/C]TTTTTGAGATGGAGT | 9100 |
| rs751079997 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84771151 | GTTATTTGTAAAGAT[A/G]CATCTTAGTGACAAA | 9100 |
| rs751096707 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84750717 | TGCTTTCAAAATTAT[A/G]CAACAGTATATTTTG | 9100 |
| rs751111306 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84777744 | CATTTAGCCCCTCCA[C/T]GTGACAACTGCGACT | 9100 |
| rs751130072 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84777604 | TGTTCAGTCTCCTCC[A/G]GGGTCCCTGCACAGA | 9100 |
| rs751135497 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84761923 | GCCCTTTTCTGCACA[C/T]GTGCAGAGCATGCAC | 9100 |
| rs751143335 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84703320 | TGATTATTGATGTCA[C/T]TTATAGTGAAATCTC | 9100 |
| rs751167011 | snp | C/G | 1.65792e-05 | 0.00287912 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764200 | CCCGGAACAAGACTT[C/G]CGTCACCCGCCAGGC | 9100 |
| rs751218775 | in-del | -/C | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698596 | TTTCTTTCTTTCTTT[-/C]TTTCTTTTTTTTTTT | 9100 |
| rs751223426 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84710463 | TCTTTTGGGGACTTT[C/T]GAGACAGATTAATGT | 9100 |
| rs751228457 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84753982 | AGGGGAGGCCTCATG[C/T]AGCTAGTAGGGATGG | 9100 |
| rs751235925 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84743236 | TCATGCATAAACTTG[A/C]TGTTAGGTGTAATCG | 9100 |
| rs751238858 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84762912 | GAGGCATGGTTGGAC[C/T]TTGCAAGTACTGCAT | 9100 |
| rs751247683 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84739377 | CCCAGGTTCAAACGA[C/T]TCTCCTGCCTTAGCC | 9100 |
| rs751254940 | snp | C/T | 3.3269e-05 | 0.00407841 | synonymous-codon, nc-transcript-variant, intron-variant | USP10 | GRCh38.p7 | 16:84759366 | GCCACTACATAGACA[C/T]TGCAGGCATTGGTTG | 9100 |
| rs751286220 | in-del | -/A | | | intron-variant | USP10 | GRCh38.p7 | 16:84702111 | CCCAGGCTGGAGTGC[-/A]AGTGGCATGATCTCG | 9100 |
| rs751299785 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84709796 | CACGGACAAGGGCAT[A/G]TGGAGGAGACTGTGC | 9100 |
| rs751308980 | snp | A/G | 1.6571e-05 | 0.0028784 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84763025 | GAATACTTAGGCTTC[A/G]TTCTAAATGGACTTC | 9100 |
| rs751346765 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84774338 | GAACAGCATGCCTCC[A/G]ACGGACTCTTGTGTC | 9100 |
| rs751352017 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84756809 | TGCTGTTCTGTGGCA[C/T]ACACTAGAAATGATA | 9100 |
| rs751383911 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84771348 | CTTAAGTCTAGGAGT[A/T]CAAGACCAGCTGGGC | 9100 |
| rs751384774 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84772409 | TCTGTGGGGCAGGAA[A/G]AGCCATGAAGTCCTG | 9100 |
| rs751394674 | snp | C/G | 1.6615e-05 | 0.00288223 | intron-variant | USP10 | GRCh38.p7 | 16:84733533 | TGTTTTAGTGAGTCC[C/G]TGGGTAGATACAATT | 9100 |
| rs751397844 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84765664 | CACAGTTTCTTTATC[C/G]ATTGGCCCATCCACA | 9100 |
| rs751447406 | snp | A/G | 0.000103422 | 0.00719028 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745273 | TGGCAGAGACACCCT[A/G]TCAAGGACAGCTGGG | 9100 |
| rs751465865 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84757772 | GGCCCTGGCTATGCT[A/C]CCTGGCTCCTGTGTG | 9100 |
| rs751487860 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84731797 | TTTTTGTGATAGTCT[C/G]TGCTAATTTTTTCTG | 9100 |
| rs751502588 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84739901 | TGCAATGTAGTGATC[A/G]TGAATAAGAGGTGCA | 9100 |
| rs751505832 | snp | C/T | 5.03681e-05 | 0.00501812 | intron-variant | USP10 | GRCh38.p7 | 16:84772714 | AAGGTCGGGAGTGTT[C/T]GTGGTGACACACTCC | 9100 |
| rs751541251 | snp | C/T | 0.000145932 | 0.00854077 | intron-variant | USP10 | GRCh38.p7 | 16:84732567 | TTCTCCTGGCTCAGC[C/T]TCCCGAGCAGCCGGG | 9100 |
| rs751547737 | snp | C/T | 1.65715e-05 | 0.00287845 | intron-variant | USP10 | GRCh38.p7 | 16:84740301 | TTGTTTTCTGATTCC[C/T]TGTGCAGCTTCCTCC | 9100 |
| rs751565854 | snp | A/G | 1.68886e-05 | 0.00290586 | intron-variant | USP10 | GRCh38.p7 | 16:84762950 | AGGCCTTTGACAGTG[A/G]TCAGTTCACAGTAAC | 9100 |
| rs751578781 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84704540 | TTATTGAAGTGTTCT[C/G]CCAAAAGGTCTTTCT | 9100 |
| rs751587623 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84742646 | GTTGTTGAAGCCAAG[C/G]GTGCAGGCCGTCCTG | 9100 |
| rs751594657 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84715692 | CTAACTGGCTTACAC[C/T]ATAAACTAGAGATTT | 9100 |
| rs751598424 | snp | A/G | 1.65712e-05 | 0.00287843 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84775176 | ACTGCTTTCTCCAGG[A/G]GTTAAAAATAAGAAT | 9100 |
| rs751617050 | snp | C/T | 1.66305e-05 | 0.00288357 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84745023 | TGGTCAATGGCCATG[C/T]CAATTCAGCAGTCCC | 9100 |
| rs751680010 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84767281 | ATGTTTCCTTGCTGA[A/G]GCTAAATGAGAGATG | 9100 |
| rs751692022 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84769718 | TTGGCCACCCATGCT[G/T]TTGGGGAGGTGGTCA | 9100 |
| rs751697315 | in-del | -/TTTA | | | intron-variant | USP10 | GRCh38.p7 | 16:84701638 | GCATAGCTCACTTCC[-/TTTA]TTTAATAAGCATCAA | 9100 |
| rs751713349 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779717 | ATTGTAACTTTATTG[A/C]CATTAAAAGATTTCA | 9100 |
| rs751784170 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84760351 | GGTAACTGTTGCTTA[C/T]TGATATTTGCCCTCT | 9100 |
| rs751801202 | snp | A/G | 1.6693e-05 | 0.00288898 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744942 | GTAAAAAGAAGAAAA[A/G]GCGGCCACCTGGATA | 9100 |
| rs751831875 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84725001 | AATTTTTATTTTGAT[A/G]TAAGTACTGACCTTT | 9100 |
| rs751840375 | snp | A/C | 3.32779e-05 | 0.00407895 | intron-variant | USP10 | GRCh38.p7 | 16:84758670 | GATTTGAATGTTCTT[A/C]ACTAGATGTCATCAA | 9100 |
| rs751842031 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84708065 | CTTGGGTGACAGAGC[A/G]AGACTCTTACGTCAA | 9100 |
| rs751867207 | snp | A/G | 4.96298e-05 | 0.00498121 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779123 | CAGTGCCCGCTTCGT[A/G]GGACACCACCTCACA | 9100 |
| rs751920301 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84711116 | AAGAGCTGTCATGTC[C/G]TGTCTTCAGAACGAG | 9100 |
| rs751935954 | snp | A/C/G | 0.000152221 | 0.00872303 | intron-variant | USP10 | GRCh38.p7 | 16:84778848 | GACCTGTAATGATTC[A/C/G]TGTGCAGTGCTGTTC | 9100 |
| rs751961546 | snp | C/T | 5.00839e-05 | 0.00500394 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745420 | AAGCATAGACTTGGA[C/T]CCAACCAAACCCGAG | 9100 |
| rs751965932 | snp | A/C | 3.16972e-05 | 0.00398091 | intron-variant | USP10 | GRCh38.p7 | 16:84768389 | ATTTTGAACCTTTCT[A/C]CTAAGGTGCTCTGGT | 9100 |
| rs751989104 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84754674 | TATCGATTTAAGGGA[A/G]TGGCTGATGTAGAAA | 9100 |
| rs751990342 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84701885 | TGCTTTTAAGTTTTA[C/G]CATGGAGAAAGTAGC | 9100 |
| rs752049258 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84766684 | GTGGAAAATACCAGC[A/G]TCCATTTGGAGGACT | 9100 |
| rs752049923 | snp | A/G | 5.02256e-05 | 0.00501102 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745360 | AATACTTGAATCCTC[A/G]GGTGAGGGCACAGCT | 9100 |
| rs752061758 | in-del | -/AT | | | intron-variant | USP10 | GRCh38.p7 | 16:84775971 | GGCTGTTTTTACTAC[-/AT]GTTTCTAGCTTCTGT | 9100 |
| rs752066675 | in-del | -/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84757977 | ATTCATAGTGGGACA[-/G]GGGGGAGACCTTGTC | 9100 |
| rs752067983 | snp | C/G | 8.2837e-05 | 0.00643519 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84759939 | AGTACCTCCAAAACC[C/G]CGACAAGGTTAGTAA | 9100 |
| rs752090661 | in-del | -/GAAGA | 1.66604e-05 | 0.00288616 | frameshift-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764127 | AACCACTCGGTCAAT[-/GAAGA]AGAGCAGGAAGAACA | 9100 |
| rs752097617 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84721902 | AGGGTTTCACCGTGT[G/T]GCCTAGGCTGATCTT | 9100 |
| rs752106311 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84714879 | AAAAACAAGTTCTAC[A/T]TATGAAATGTTTGAA | 9100 |
| rs752119669 | in-del | -/TT | | | intron-variant | USP10 | GRCh38.p7 | 16:84723884 | CCTTGCAGCCTCTTC[-/TT]TTGTTCGTCCTTGGC | 9100 |
| rs752218255 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84704062 | CAAGCCTAAGCGGCA[C/G]GTTGCACTGTGCTGT | 9100 |
| rs752246487 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84776202 | CTGGCCTGCAGTGGC[A/G]GAGCAGGGCTTCAAG | 9100 |
| rs752283254 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84724448 | AGAATATACAAACAG[G/T]GAAGTAGACACTCAA | 9100 |
| rs752306887 | in-del | -/CC | | | intron-variant | USP10 | GRCh38.p7 | 16:84770769 | AGAGCGAGACTCCGT[-/CC]CCAAAAAAAAAAAAA | 9100 |
| rs752322061 | snp | A/C/T | 3.31731e-05 | 0.00407255 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744779 | ACAGCTTCCAAAATA[A/C/T]CCCCTGATGGTATCA | 9100 |
| rs752334811 | snp | C/G/T | 3.31638e-05 | 0.00407198 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744704 | ACTTTGCCGAGAACC[C/G/T]CCAGCTACAGTATTT | 9100 |
| rs752342341 | snp | A/G | 1.68196e-05 | 0.00289992 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764113 | CCAACGGCCCCAAAA[A/G]CCACTCGGTCAATGA | 9100 |
| rs752346121 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84717013 | ATGAGATAGAGCATA[A/G]CAGTGCTTCTCAAAC | 9100 |
| rs752357545 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84761244 | GAGGGGCCCACCTAG[C/T]ACAGGTGGAGGCAAA | 9100 |
| rs752412442 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84742501 | CCCCTGCCTTGTAGT[C/G]CAGTCCTCTCTACTG | 9100 |
| rs752419940 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84773096 | CCCTTCTAACCTCTA[G/T]TTGTGGTGGCGCACA | 9100 |
| rs752431832 | in-del | -/TTCTTT | | | intron-variant | USP10 | GRCh38.p7 | 16:84732442 | AATGACTTCTTCTTC[-/TTCTTT]TTTTTTTTTTTCTTT | 9100 |
| rs752442371 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84712268 | CCTTGTGGTCCTGTC[C/G]TGAGAGTAGCGGAAG | 9100 |
| rs752467229 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84705043 | TCTCCTCCCCGTTGG[A/G]CTTGTGTGTACAGCC | 9100 |
| rs752507493 | snp | A/G | 1.66034e-05 | 0.00288122 | intron-variant | USP10 | GRCh38.p7 | 16:84733524 | ACAAAACTTTGTTTT[A/G]GTGAGTCCGTGGGTA | 9100 |
| rs752588149 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84773822 | CTCGGCCTCTGCTCC[C/T]GCATCTTCACTCGCC | 9100 |
| rs752635266 | in-del | -/AAA | | | intron-variant | USP10 | GRCh38.p7 | 16:84746977 | TAACTTTTTAAACTT[-/AAA]AAAAAGTAAGACACA | 9100 |
| rs752675770 | in-del | -/T | 1.65658e-05 | 0.00287795 | frameshift-variant, intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84740353 | GGCACACAGGCTGTG[-/T]GATAAACTACCTGAT | 9100 |
| rs752699446 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84756740 | GACACTATGCCTTTA[C/T]GTCATTGATGGTTAT | 9100 |
| rs752715640 | snp | A/G | 1.7479e-05 | 0.00295621 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745210 | TGCAGGGCAGCCAGA[A/G]GGGGGCCCCGGGGCT | 9100 |
| rs752727245 | snp | C/G | 3.31208e-05 | 0.00406931 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84772585 | AAAACTCCCTCCTGT[C/G]CTCGTGCTGCACCTG | 9100 |
| rs752727673 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84721847 | GGACTACAGGCACAC[A/G]CCGCCACACCTGGCT | 9100 |
| rs752735237 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84712888 | ATAGGACACTTAGCA[A/T]TGCAGAGAGAATGCC | 9100 |
| rs752762570 | snp | G/T | 2.33364e-05 | 0.0034158 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745649 | GTTCCGGTTTCAGAG[G/T]ATCCTGTAGCCATAA | 9100 |
| rs752801854 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84701763 | TTTACGTTTTATACA[A/G]CAGTCTAAAGCGTTA | 9100 |
| rs752810447 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84767232 | ACTAGGTCACCGAGA[A/C]TGCAGAAATAGAAGC | 9100 |
| rs752811748 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84774764 | GTGAGCCACCGTGCC[C/T]GGCCTGTAATTGAAG | 9100 |
| rs752814799 | snp | G/T | 1.66668e-05 | 0.00288672 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744875 | AGTTCTAATGTGGAG[G/T]CGGAAGTTTTGGAAA | 9100 |
| rs752825228 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84755846 | TTTAATATACATATA[C/T]GATTTACTGGTGTCA | 9100 |
| rs752828300 | snp | A/G | 1.6908e-05 | 0.00290753 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779092 | CTGTAAACCCTGTGT[A/G]CGCTGTGTGTGCGCC | 9100 |
| rs752886418 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84748248 | TATAATGAGAAATGC[A/G]TGGTGGGGTCCTGTT | 9100 |
| rs752889352 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84739995 | CTGACATCCTGTGGA[A/T]AGAAGGATGTATCAT | 9100 |
| rs752911087 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84758953 | TGGTCTGCCTACCTT[G/T]CTTATAAACAGGATT | 9100 |
| rs752960644 | snp | C/T | 0.000185175 | 0.00962046 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745592 | CCTCCCGCCATATCT[C/T]CCCTGGTTTCTGAAA | 9100 |
| rs752996511 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84729707 | TGTAACTGCTCACTT[C/T]TAAAAGCTCATGCAT | 9100 |
| rs753037981 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84736227 | TCTAGTCGAATTTTT[C/G]ATATGCTTTTTCTCC | 9100 |
| rs753048530 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84770956 | ATGTAGTCCCAGCCT[C/T]TCAGGAGGCTGAATC | 9100 |
| rs753073688 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84709206 | CACAGTTACGTACAC[A/G]TCACTCCAAACTGAG | 9100 |
| rs753082570 | snp | C/T | 0.00197044 | 0.0313263 | intron-variant | USP10 | GRCh38.p7 | 16:84732490 | CTGGCTCTGTCGCCC[C/T]GGCTGGGGTGCGGTG | 9100 |
| rs753103390 | snp | A/G | 1.65693e-05 | 0.00287826 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84759924 | GTTCACTAATATGCC[A/G]GTACCTCCAAAACCC | 9100 |
| rs753103750 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84761821 | AGACACCAGCCAAGG[A/G]GCAACCTTGCAAGCA | 9100 |
| rs753126580 | snp | A/G | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699350 | GGCTGGTTTGCCCGT[A/G]CACACGCACGCACGT | 9100 |
| rs753146541 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84713386 | TACCCACCTTTAAAA[-/T]TGCGCCCTCCTTCAC | 9100 |
| rs753153944 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84747120 | ACCGAAATGTTACGC[C/T]GCGCGTGACTGTACG | 9100 |
| rs753172108 | snp | C/G | 0.000597669 | 0.0172765 | intron-variant | USP10 | GRCh38.p7 | 16:84700155 | AAGGGGCCCGAGCCC[C/G]GGGCGGGCGGACGCC | 9100 |
| rs753182394 | snp | C/G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84729004 | GATTTCACCATTTTG[C/G/T]CTGGGCTGGTCTTGA | 9100 |
| rs753187888 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84774616 | GCTGAGACTACAGCC[A/G]CGTGCCACCACGCCC | 9100 |
| rs753206149 | snp | A/G | 1.67598e-05 | 0.00289476 | intron-variant | USP10 | GRCh38.p7 | 16:84764279 | GTTTGTGCTTTTCTG[A/G]AATAACTTAATATTT | 9100 |
| rs753246518 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84721220 | TTTAAGATGATGTTG[C/T]GTAGCACTGGGAGGT | 9100 |
| rs753282506 | snp | C/T | 0.000309054 | 0.012427 | intron-variant | USP10 | GRCh38.p7 | 16:84764043 | TTTTTTTTTTGCTGT[C/T]CTTGTCGTAAATAGT | 9100 |
| rs753300977 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84724292 | TAATTTGGAGATTCA[A/G]TCTGAATTCAATCTA | 9100 |
| rs753310040 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84712153 | AGAAGGGAAAGAAAT[C/T]GCAGTATTTTGTGTG | 9100 |
| rs753321845 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84730024 | AAGGTGATTTCTGTT[G/T]TGTTTACTTTTTATG | 9100 |
| rs753359762 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84703337 | TATAGTGAAATCTCC[A/G]CAATAATGCTTCCTA | 9100 |
| rs753372836 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84749602 | AATTATACACACACA[A/C]AATGCTTGGAATAAT | 9100 |
| rs753383327 | snp | A/G | 1.88931e-05 | 0.00307346 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84778901 | CTCTTCCAGTGGTCT[A/G]CCATCACGGCAACAG | 9100 |
| rs753428583 | snp | C/G | | | missense, intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84704844 | TGCCCTGGTTGCCCT[C/G]TCCTGGAATAGGGCA | 9100 |
| rs753461604 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84755597 | GGCATAATCACGCCA[C/T]TGCACTCCAGCCTGG | 9100 |
| rs753463221 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84764435 | CCCTTGTCAGCCCCC[A/G]TGGCTTATTCTCTCC | 9100 |
| rs753468567 | snp | A/G | 1.6659e-05 | 0.00288604 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745402 | GGAGTTGCACACCAC[A/G]GAAAGCATAGACTTG | 9100 |
| rs753476788 | in-del | -/AA | | | intron-variant | USP10 | GRCh38.p7 | 16:84755797 | AGTGAGACTGTCTCA[-/AA]AAAAAAAAAAAAAAT | 9100 |
| rs753476963 | snp | A/G | 3.3543e-05 | 0.00409516 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745348 | TGCTAATGGACAAAT[A/G]CTTGAATCCTCGGGT | 9100 |
| rs753480863 | snp | A/G | 3.31752e-05 | 0.00407265 | intron-variant | USP10 | GRCh38.p7 | 16:84775270 | CATTAAAACACTGAT[A/G]AAGGGGTTTACAGCT | 9100 |
| rs753483295 | in-del | -/GTT | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84719100 | CCGGCCAGTTTAGTT[-/GTT]GTTGTTGTTGTTGTT | 9100 |
| rs753487220 | snp | A/G | 1.65652e-05 | 0.0028779 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84775206 | TTTTAAATGCCACCG[A/G]ACCTATCGGCTCTTT | 9100 |
| rs753514552 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84756561 | TTGCACCACTGCACT[C/G]CAGCCTGGGTGACAG | 9100 |
| rs753517631 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84726098 | TCTTACTTCAGGGCT[A/G]ATCTCCTATTTCTAT | 9100 |
| rs753548159 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84707354 | AAAGTTTGTGTGGGG[A/T]ACATTTTAATAAAGT | 9100 |
| rs753556391 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84703901 | CTAAGCGGGCCTACC[A/G]CATTCTAAATTCCTC | 9100 |
| rs753569021 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84778833 | AGGGAAGTCGGCGGA[G/T]ACCTGTAATGATTCG | 9100 |
| rs753586082 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84723525 | TGGGAAGTCACAATG[A/G]TTGCTATGTAGTTTG | 9100 |
| rs753625125 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84734462 | TTATATCCCTTGTCC[A/G]TATTTTTAAATCAAG | 9100 |
| rs753660452 | snp | A/G | 1.70095e-05 | 0.00291625 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745148 | TCTGTCAGTGACATT[A/G]TGCCTGACAGTCCTT | 9100 |
| rs753673869 | in-del | -/TT | 0.00021798 | 0.0104376 | intron-variant | USP10 | GRCh38.p7 | 16:84764286 | CTTTTCTGGAATAAC[-/TT]AATATTTGCCTTTTC | 9100 |
| rs753714255 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779641 | TACTGAGAGAAACTG[C/T]TTACGTACACATTGC | 9100 |
| rs753766841 | snp | C/T | 6.64088e-05 | 0.00576194 | intron-variant | USP10 | GRCh38.p7 | 16:84758689 | AGATGTCATCAATTT[C/T]TGAAATATGCTTCTT | 9100 |
| rs753785898 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84763177 | TGTTGCTTCCCTGCC[C/T]CTCAGTCGTTTTCCT | 9100 |
| rs753792628 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84744497 | CGCAAATTGTTCAGC[A/G]TAAGTAAAGGACGTA | 9100 |
| rs753805093 | in-del | -/CTC | | | intron-variant | USP10 | GRCh38.p7 | 16:84733147 | TGAACCAATAAAAAT[-/CTC]CTGCAAGCAGGACTC | 9100 |
| rs753807337 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84726705 | GCCCGGGATGGAGGC[C/T]GGATGGGATATGAGG | 9100 |
| rs753819437 | in-del | -/CAAAAAA | | | intron-variant | USP10 | GRCh38.p7 | 16:84770772 | GCGAGACTCCGTCCC[-/CAAAAAA]AAAAAAAAAAAATCT | 9100 |
| rs753822988 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84711324 | GCTCTGCACCCCACA[C/T]CTTGAAATAGGACCT | 9100 |
| rs753832309 | snp | G/T | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699148 | AACCTCACAGAAATC[G/T]TACGCGTTATGACAT | 9100 |
| rs753833999 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84737433 | TCTGTTGTGTATTTA[G/T]ATACCCAGTTACCAC | 9100 |
| rs753836912 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84763700 | GTTGCGATTGGTTGC[C/T]GTGGATCAAGTGGCA | 9100 |
| rs753841188 | in-del | -/GTT | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84719098 | CGCCCGGCCAGTTTA[-/GTT]GTTGTTGTTGTTGTT | 9100 |
| rs753855157 | snp | C/T | 3.33533e-05 | 0.00408357 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84745062 | TCAGTGCAGAGGATG[C/T]AGAATTTATGGGTGA | 9100 |
| rs753855218 | snp | C/T | 1.65685e-05 | 0.00287819 | intron-variant | USP10 | GRCh38.p7 | 16:84758813 | CATTAATGCTGTATC[C/T]TTCCTGGACGCCGTC | 9100 |
| rs753866479 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84719038 | CTCAAATGATCCACC[C/T]GTCTCGGCCTCCCAA | 9100 |
| rs753898698 | snp | A/G | 4.61074e-05 | 0.0048012 | intron-variant | USP10 | GRCh38.p7 | 16:84760308 | TGTCACTAGTATCAA[A/G]TGTTGCCTTTTGTTC | 9100 |
| rs753938051 | snp | C/T | 1.71082e-05 | 0.00292469 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745484 | GCATCAGGCACCCTT[C/T]CTGTCAGCCAGCCCA | 9100 |
| rs753973600 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84700692 | TTGCAAAGAAAACTC[A/G]AAATAAGTCGCAAGG | 9100 |
| rs753996484 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84774384 | TCTGCGCACAGTAAG[A/G]GCAGGGAGTTCCCGC | 9100 |
| rs754004519 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84753656 | TGCCCTTTACTGTGC[A/G]TCTTCTCAGGAGCTG | 9100 |
| rs754016148 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84755656 | TAATAATTATGATTG[A/G]GTATGGTGGCACACA | 9100 |
| rs754019459 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84766413 | TGGTTCCTTGGGACA[A/C]GTCGTGTTGGGAGGG | 9100 |
| rs754040585 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84746005 | TTTTCTGTGATATAC[C/T]TTTGGTATGATAATC | 9100 |
| rs754050695 | snp | A/G | 5.18041e-05 | 0.00508914 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745182 | CCGGAGCACTCGGCA[A/G]TGACACCAGGACTGC | 9100 |
| rs754073425 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84758055 | CAGCTGTTTTAATAC[A/G]CAGAAAGAGTGATGT | 9100 |
| rs754093408 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84746934 | TATTCTTACTTTCCT[A/G]TAAGCTTTTTCATAT | 9100 |
| rs754095920 | snp | A/G/T | 0.000216138 | 0.0103935 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84760227 | TGCCTTTGAGCCCAC[A/G/T]TATATTTACAGACTC | 9100 |
| rs754117042 | snp | C/T | 1.66015e-05 | 0.00288105 | intron-variant | USP10 | GRCh38.p7 | 16:84733515 | TGAGGTAAGACAAAA[C/T]TTTGTTTTAGTGAGT | 9100 |
| rs754139180 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84701836 | GTAAATGTTAGCAAC[A/G]CTTTGGGTTTATTCT | 9100 |
| rs754148551 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84739969 | GTGTCTGTGGTCTGG[A/C]TGGTCAGTCACTGAC | 9100 |
| rs754185805 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84768635 | GGCAATCTAATGATG[A/G]TATCACAACATCAAT | 9100 |
| rs754204047 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84724294 | ATTTGGAGATTCAAT[C/T]TGAATTCAATCTAAA | 9100 |
| rs754206084 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84716640 | GACTTCTTCAGAGCA[C/T]GGGGGAAGAGGGAGC | 9100 |
| rs754221380 | snp | C/T | 1.67351e-05 | 0.00289263 | intron-variant | USP10 | GRCh38.p7 | 16:84764273 | CATCAGGTTTGTGCT[C/T]TTCTGGAATAACTTA | 9100 |
| rs754227702 | snp | C/T | 8.22318e-05 | 0.00641164 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745579 | AACTAAGTATTCCCC[C/T]CCCGCCATATCTCCC | 9100 |
| rs754237031 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84769417 | GACTTGCATCTCATG[G/T]GTGATTTTGTTTAAA | 9100 |
| rs754237676 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84708176 | GAGGTCTGGCTGGGC[A/G]TGGTGGCTCACGCGT | 9100 |
| rs754241392 | in-del | -/AA | | | intron-variant | USP10 | GRCh38.p7 | 16:84714870 | AGTAATATCAAAAAC[-/AA]GTTCTACATATGAAA | 9100 |
| rs754246122 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780320 | TCTGAGACGGAAGAC[A/G]TGGAGAGAGGGATGT | 9100 |
| rs754254634 | snp | A/G | 1.65745e-05 | 0.00287871 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779010 | CAAGGTGATCAACCA[A/G]TACCAGGTGGTGAAA | 9100 |
| rs754268495 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84760676 | TTATGTCTTCATCAT[A/G]CTTACAGGCTTTAGT | 9100 |
| rs754303436 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84752815 | GAAATGAGTCAGGAT[A/G]GAAGGCTTAGTGTAC | 9100 |
| rs754309906 | snp | C/T | 6.07847e-05 | 0.00551259 | intron-variant | USP10 | GRCh38.p7 | 16:84700120 | CCCGCAGGTAGCCGC[C/T]GGTCTGCGCCTTCGG | 9100 |
| rs754331336 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84735446 | TGAAGGCCTGGGGTC[A/G]CTTCAGTTCTGCCAC | 9100 |
| rs754336406 | snp | A/G | 3.32712e-05 | 0.00407854 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744857 | GCCCTCGCTTTGGAT[A/G]GAAGTTCTAATGTGG | 9100 |
| rs754348483 | snp | A/G | 1.65825e-05 | 0.00287941 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764205 | AACAAGACTTCCGTC[A/G]CCCGCCAGGCGGATT | 9100 |
| rs754364959 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84709092 | GTGGCTGCTGTGTAC[C/G]AGGCACTGAGGAGGG | 9100 |
| rs754371972 | snp | A/C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84736119 | GAGGGCGTGTCACTT[A/C/T]TACAGCACAGTTTGG | 9100 |
| rs754441680 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84775410 | AGATGACGGATTATC[A/G]TCTTGGCCCTGAGGA | 9100 |
| rs754442168 | snp | C/G | 2.84523e-05 | 0.00377165 | intron-variant | USP10 | GRCh38.p7 | 16:84764044 | TTTTTTTTTGCTGTT[C/G]TTGTCGTAAATAGTA | 9100 |
| rs754485015 | in-del | -/G | 0.000183167 | 0.00956817 | intron-variant | USP10 | GRCh38.p7 | 16:84733121 | GTAAATGGAACAACT[-/G]GCAGTATTTGTGAAC | 9100 |
| rs754532653 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84749388 | TGCATTAGTATCTAA[C/G]TGTTTCTACTGAGAC | 9100 |
| rs754551867 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84748870 | GGAAAGCCTTGCCAC[A/G]CACAGTCCACGTAAT | 9100 |
| rs754564761 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84716576 | AAATAGGGTTTAGAA[A/G]CACTTCCTGAGGAGG | 9100 |
| rs754585916 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84722759 | GAGATGGAGTTTCAC[C/T]ATGTTGGCCAGTCTC | 9100 |
| rs754599310 | snp | G/T | 1.85699e-05 | 0.00304707 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744633 | TTTCTTTCTAAACAG[G/T]ACAAGAATATCAGAG | 9100 |
| rs754604769 | snp | A/G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84741424 | AGTGGGACTTCCTCT[A/G/T]TCACTGTGTGCTTTG | 9100 |
| rs754621275 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84723559 | AAATTATTCCTTATC[A/C]TTAGATAAGCTTTTT | 9100 |
| rs754656504 | in-del | -/ATT | | | intron-variant | USP10 | GRCh38.p7 | 16:84714913 | ATTTAAAAAGTTCTG[-/ATT]ATTATTATTATTATT | 9100 |
| rs754692218 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84716663 | GAGGGAGCTGCCTGC[A/G]CGAAGGCTGATCAGC | 9100 |
| rs754705826 | snp | A/C | 9.95405e-05 | 0.0070541 | intron-variant | USP10 | GRCh38.p7 | 16:84772497 | GGTGTTAGCTGTTGC[A/C]AGTAAGACAGGGACG | 9100 |
| rs754786062 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84721272 | ACTAAAAATCCCAGA[A/G]TGTGGATGCCTACAA | 9100 |
| rs754803237 | snp | C/T | 1.66308e-05 | 0.00288359 | missense, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84733435 | CTTATTTTTTTTCAG[C/T]ATATTTTTGGAGATT | 9100 |
| rs754821231 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84763215 | AGCATTTATTCCCTA[C/T]GATAACTTACACCAT | 9100 |
| rs754898207 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84712156 | AGGGAAAGAAATCGC[A/G]GTATTTTGTGTGTAT | 9100 |
| rs754930676 | snp | A/G | 1.66751e-05 | 0.00288744 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84745065 | GTGCAGAGGATGCAG[A/G]ATTTATGGGTGACAT | 9100 |
| rs754931547 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84702473 | TGAGCGTTTTAATAA[A/G]TTTGTTTTACTTGGT | 9100 |
| rs754942032 | snp | C/T | 1.67747e-05 | 0.00289605 | intron-variant | USP10 | GRCh38.p7 | 16:84733386 | TTTTTTCTGAAAGTA[C/T]ATAATTTGTATATTT | 9100 |
| rs754960447 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84774409 | TCCCGCCTCGTAGCA[C/G]CTGGTAGACTGGTTC | 9100 |
| rs754972158 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84710721 | ATTGGATTTAACAGC[A/G]TTTTTAGGTTTGTGA | 9100 |
| rs755017638 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84765855 | TTGCTCATTCACAAA[G/T]TCCTTCGGAAAGGTT | 9100 |
| rs755020060 | snp | A/G | 4.97657e-05 | 0.00498802 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744801 | ATGGTATCACTAAAG[A/G]AGCAAGCTATGGCTC | 9100 |
| rs755020243 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84763731 | TTGCAATGGGTTGCA[A/G]TGGATCCAGTGGCAT | 9100 |
| rs755035047 | snp | C/G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84764999 | ACATAAAACCACCTC[C/G/T]GGGAGGCAGAGGTTG | 9100 |
| rs755094713 | snp | C/G | 1.87732e-05 | 0.0030637 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745581 | CTAAGTATTCCCCTC[C/G]CGCCATATCTCCCCT | 9100 |
| rs755098149 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84746225 | AGAGTGCTAAGGCTC[A/C]AAAGTAGAAACAATT | 9100 |
| rs755124325 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84713583 | TTGTTCACTGCTGGG[A/G]CCCCTAGTCCTAGAA | 9100 |
| rs755137596 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84774539 | GCAGTGGCGCGATCT[C/T]GGCTCGCTGCAACCT | 9100 |
| rs755145646 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84713050 | TGCAAGAACCATGGA[A/G]CAGCCAGCCTTTCCA | 9100 |
| rs755147044 | snp | C/G | 1.6574e-05 | 0.00287867 | stop-gained, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779013 | GGTGATCAACCAGTA[C/G]CAGGTGGTGAAACCA | 9100 |
| rs755153236 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84747044 | AAGACGCCACTAGGC[A/G]GCAGGACGTTTCAGT | 9100 |
| rs755204556 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84739987 | GTCAGTCACTGACAT[C/G]CTGTGGAAAGAAGGA | 9100 |
| rs755220142 | snp | A/G | 1.71829e-05 | 0.00293106 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745494 | CCCTTCCTGTCAGCC[A/G]GCCCAAGTCCTGGGC | 9100 |
| rs755230521 | snp | C/T | 1.67391e-05 | 0.00289297 | intron-variant | USP10 | GRCh38.p7 | 16:84764274 | ATCAGGTTTGTGCTT[C/T]TCTGGAATAACTTAA | 9100 |
| rs755275321 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84760702 | TTAGTAGCTATTTGA[G/T]GTACTTGATTCCTTT | 9100 |
| rs755277735 | snp | G/T | | | utr-variant-5-prime, intron-variant | USP10 | GRCh38.p7 | 16:84704818 | CCATTCTGTCCCGTC[G/T]TGAAACATCATGCCC | 9100 |
| rs755302859 | snp | A/G | 4.97154e-05 | 0.0049855 | synonymous-codon, nc-transcript-variant, intron-variant | USP10 | GRCh38.p7 | 16:84759392 | GGTTGCTTGCCCGCC[A/G]ATGTACCACCTGATG | 9100 |
| rs755306546 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84735199 | CCAGGCCCGGGTGGT[A/G]TGTGTGTGTGTGTGT | 9100 |
| rs755309062 | in-del | -/CTT | | | intron-variant | USP10 | GRCh38.p7 | 16:84748385 | TCGGCTCACTGCAAC[-/CTT]CTTCTCCTCCTGGGT | 9100 |
| rs755318099 | snp | C/T | 0.000660978 | 0.0181673 | intron-variant | USP10 | GRCh38.p7 | 16:84759517 | TGGTGGGGTTTTTCC[C/T]GTCTGATAATTAGAA | 9100 |
| rs755326411 | in-del | -/A | | | intron-variant | USP10 | GRCh38.p7 | 16:84742159 | ATACAGGCATACAAC[-/A]AGTAATAATCACATC | 9100 |
| rs755334087 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84734730 | CATCCTTTAGATAAC[A/G]AAGATATTTGTCTGT | 9100 |
| rs755374850 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84735549 | TTTTAAATTGAAAAA[A/C]TGCAGAATGCTTATT | 9100 |
| rs755420713 | snp | A/G | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698080 | CCAAGTGCAGATATC[A/G]CTTTTCCATGGTTAA | 9100 |
| rs755428270 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84727750 | TGAGATTTCAGGGAA[C/G]ATTACATACACTGTA | 9100 |
| rs755463956 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84716998 | GAGCTTCGGGATTAC[A/C]TGAGATAGAGCATAG | 9100 |
| rs755493304 | snp | C/T | 1.65847e-05 | 0.0028796 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764207 | CAAGACTTCCGTCAC[C/T]CGCCAGGCGGATTTT | 9100 |
| rs755514549 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84720285 | AGCTGGCCTTCTGTT[A/G]GTCCGGTTCCAGCGT | 9100 |
| rs755520193 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84709158 | GAGGAGTTTATGGGT[C/G]CATTGAGGAAGACAG | 9100 |
| rs755524390 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780353 | CGTGCAAGGGTGCCC[A/G]TGCCCCGGCTTCTGG | 9100 |
| rs755528568 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84733265 | CAGTAGTATTTCTTT[C/T]ATATAAACAACCTAG | 9100 |
| rs755541381 | snp | A/G | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699264 | CCCAAGGGTGGACCC[A/G]CTGGCTGGAAAACAG | 9100 |
| rs755576229 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84736935 | CTGGGACTACAGGCG[C/T]CCGCCACCTCGCCCG | 9100 |
| rs755589457 | snp | A/G | 1.6566e-05 | 0.00287797 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84775202 | AGAATTTTAAATGCC[A/G]CCGAACCTATCGGCT | 9100 |
| rs755662083 | snp | C/T | | | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84763071 | ACCTAAAGAAGCTTC[C/T]CTCACCAAGTAATGA | 9100 |
| rs755663724 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84755561 | CAATCTGTTGAACCC[A/T]GGAGGTCGAGGCTGC | 9100 |
| rs755689407 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84711217 | CTCTGTGCCAGGGCC[C/T]GTGTTGGGATTTATA | 9100 |
| rs755705884 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84731749 | AGTAATTAATTTCCG[C/T]GAACACTTTCATGAT | 9100 |
| rs755713358 | snp | C/G | 1.6577e-05 | 0.00287893 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84763058 | GAGGAAATGTTGAAC[C/G]TAAAGAAGCTTCTCT | 9100 |
| rs755726448 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84748408 | TCCTGGGTTCAGGCA[A/G]TTCTCCTGCCTCAGC | 9100 |
| rs755735829 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84729294 | GCCAAGAAAGAAATA[C/T]TTATCGTTTTTCAAA | 9100 |
| rs755757636 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84703256 | GTTAAATTATTTGGG[A/G]TAATTAATTTGAAGC | 9100 |
| rs755786718 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84722097 | TCTTCATGCCCCTTT[A/G]CCATGAATCCCCACC | 9100 |
| rs755788815 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84729944 | AAGCTGTTGTCAATG[A/T]GCTCTTGAAACTAAC | 9100 |
| rs755799564 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84748353 | CTGTCGCCCAGGCCG[C/G]AATGCAGTGGCGCAA | 9100 |
| rs755806003 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84775391 | TTTACCTGAAACTCT[A/G]CGTAGATGACGGATT | 9100 |
| rs755834489 | snp | C/T | 1.65658e-05 | 0.00287795 | missense, intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84740343 | CAGTTCTGTGTGGCA[C/T]ACAGGCTGTGGATAA | 9100 |
| rs755840248 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84722691 | TAGCCTCCCGAGTAG[C/G]TGGGATTACAGGCAG | 9100 |
| rs755859320 | snp | A/C | 0.000192704 | 0.00981402 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779131 | GCTTCGTAGGACACC[A/C]CCTCACACTCACTTC | 9100 |
| rs755872051 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84778648 | TATGTGGTTAATATG[C/T]GTACATGCACACATG | 9100 |
| rs755882087 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84750166 | TAATCCCAGCACTTT[C/T]GGAGGTTGAGGTGGG | 9100 |
| rs755901509 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84777916 | TGCCGGACAGCCGCC[G/T]TCCCGAGGCTGGTGT | 9100 |
| rs755936108 | in-del | -/ATAAAC | 1.65658e-05 | 0.00287795 | cds-indel, intron-variant | USP10 | GRCh38.p7 | 16:84740355 | GCACACAGGCTGTGG[-/ATAAAC]TACCTGATGGTAAGC | 9100 |
| rs755948071 | snp | A/G | 1.6666e-05 | 0.00288664 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84745055 | AACAGTGTCAGTGCA[A/G]AGGATGCAGAATTTA | 9100 |
| rs755957028 | in-del | -/AG | | | intron-variant | USP10 | GRCh38.p7 | 16:84757236 | CGGTATTCCATATTA[-/AG]AGAGAGAGGAGCTTT | 9100 |
| rs755964823 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84725982 | CCACTGTGAGGCTTA[C/G]CTGTGCATCTGTGAA | 9100 |
| rs755980632 | snp | C/G | 2.65911e-05 | 0.00364621 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84768290 | AAGATACGCACAGTC[C/G]AGGATGCACTGGAGA | 9100 |
| rs755989636 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84771432 | CCCAGGAAGTCAAGG[C/T]TGCAGTGAGTCCTCA | 9100 |
| rs756012947 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717587 | GTCAGCATTTGCTAG[A/T]CTCTTAGGTGCCAAG | 9100 |
| rs756067776 | in-del | -/TC | 1.66355e-05 | 0.002884 | frameshift-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764131 | CTCGGTCAATGAAGA[-/TC]AGAGCAGGAAGAACA | 9100 |
| rs756094949 | snp | C/G | 1.6604e-05 | 0.00288127 | intron-variant | USP10 | GRCh38.p7 | 16:84764039 | CCTTTTTTTTTTTTG[C/G]TGTTCTTGTCGTAAA | 9100 |
| rs756096948 | snp | A/G | 2.63314e-05 | 0.00362836 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745666 | TCCTGTAGCCATAAA[A/G]ATTGCAGGTATAGTT | 9100 |
| rs756110445 | snp | A/C | | | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780276 | AGCGGTGCCTCCAGA[A/C]GCCACCCTCAGTAGT | 9100 |
| rs756186970 | snp | C/T | 4.98591e-05 | 0.0049927 | intron-variant | USP10 | GRCh38.p7 | 16:84758679 | GTTCTTCACTAGATG[C/T]CATCAATTTCTGAAA | 9100 |
| rs756189114 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84762103 | CAGAATCAAACACTC[A/G]TGATGTGGGATTATT | 9100 |
| rs756204719 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84773877 | TTGGATGTTTTGCTA[C/T]AGTGATTTTATTTTT | 9100 |
| rs756208262 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84727642 | TGGAATTCTCTGTCT[A/G]CAAATACACACTCAT | 9100 |
| rs756214873 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84708488 | ATTCACATTCAGATT[C/G]TTGTCCATCCATTGC | 9100 |
| rs756235215 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84738458 | ACAGAGGGTTTTGAA[C/T]GAGATGGAGGCTTCC | 9100 |
| rs756257535 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84720230 | AAGAGGAAGCTCTGC[C/T]GTGGCGATGTGCGTT | 9100 |
| rs756284995 | snp | C/G | 5.01065e-05 | 0.00500507 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745425 | TAGACTTGGACCCAA[C/G]CAAACCCGAGAGTGC | 9100 |
| rs756314264 | snp | A/G | 0.000104075 | 0.00721293 | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84733072 | TTTGGCAGAGAAAGC[A/G]GAAATGGAGGTAGTG | 9100 |
| rs756333241 | snp | A/T | 1.66801e-05 | 0.00288787 | intron-variant | USP10 | GRCh38.p7 | 16:84733423 | ATCAGTGACTCTCTT[A/T]TTTTTTTTCAGTATA | 9100 |
| rs756348853 | snp | A/C | 1.65685e-05 | 0.00287819 | intron-variant | USP10 | GRCh38.p7 | 16:84759950 | AACCCCGACAAGGTT[A/C]GTAAAAATGAGTTTT | 9100 |
| rs756356395 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84772895 | GCAAAAATAACTAAA[C/T]TCTATAATCTTACTA | 9100 |
| rs756380099 | snp | A/G | 0.000381183 | 0.0138002 | missense, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779006 | CAGTCAAGGTGATCA[A/G]CCAGTACCAGGTGGT | 9100 |
| rs756383920 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84752227 | CCCCACCAACTCCTG[A/T]GACAAAGATGGACTG | 9100 |
| rs756386359 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84767442 | GTTAACTTGTTTTTT[A/G]TTCTACACACCCTAC | 9100 |
| rs756407202 | in-del | -/CAGC | | | intron-variant | USP10 | GRCh38.p7 | 16:84703802 | TACAGATGGCCTGAG[-/CAGC]CAGCCGCGCCGTACC | 9100 |
| rs756426270 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84712950 | TGGGGGCTCCGTGTA[C/T]TAAAGCTCTTCCAGG | 9100 |
| rs756465382 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84730123 | CCCTCCACTCCTGTC[G/T]GCGTCCACTCAGCGT | 9100 |
| rs756497290 | in-del | -/AGGGCCCGT | | | intron-variant | USP10 | GRCh38.p7 | 16:84754479 | CTAGTACACGTCCCA[-/AGGGCCCGT]ACGTATGTTCTGCTG | 9100 |
| rs756505144 | snp | A/G | 4.97459e-05 | 0.00498703 | intron-variant | USP10 | GRCh38.p7 | 16:84758830 | TCCTGGACGCCGTCC[A/G]CAAGGCCAGCTTGTT | 9100 |
| rs756505225 | snp | C/T | 1.65795e-05 | 0.00287914 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764201 | CCGGAACAAGACTTC[C/T]GTCACCCGCCAGGCG | 9100 |
| rs756610797 | snp | A/C | 3.42038e-05 | 0.0041353 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745481 | TCTGCATCAGGCACC[A/C]TTCCTGTCAGCCAGC | 9100 |
| rs756619709 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84735392 | AAAACTTGAGTTTTC[A/G]TGTGATAGGAAAGTG | 9100 |
| rs756643987 | snp | C/T | 5.19107e-05 | 0.00509438 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84778926 | CAACAGTGCGACGGG[C/T]GGCCATTACACTACA | 9100 |
| rs756651985 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84726879 | TGCAACCACAGGACG[C/T]GGGAAAGGAGCGTTT | 9100 |
| rs756667613 | snp | C/G | 1.65773e-05 | 0.00287895 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744714 | GAACCCCCAGCTACA[C/G]TATTTCAAGCACACT | 9100 |
| rs756731114 | snp | A/C | 5.16436e-05 | 0.00508125 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745277 | AGAGACACCCTGTCA[A/C]GGACAGCTGGGGCTC | 9100 |
| rs756779814 | snp | A/T | 1.65608e-05 | 0.00287752 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84772599 | TCCTCGTGCTGCACC[A/T]GAAACGATTCGTTTA | 9100 |
| rs756797468 | snp | A/G | 1.6615e-05 | 0.00288223 | intron-variant | USP10 | GRCh38.p7 | 16:84733537 | TTAGTGAGTCCGTGG[A/G]TAGATACAATTAATA | 9100 |
| rs756865496 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84736333 | GGATGTTAAGATGAA[A/G]GAGCATTCTGCCTTC | 9100 |
| rs756869643 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84743278 | CTTTTCCAGGAACTT[C/T]CTCTTGTTGGGGCAG | 9100 |
| rs756871723 | snp | A/G | 1.67936e-05 | 0.00289767 | intron-variant | USP10 | GRCh38.p7 | 16:84772715 | AGGTCGGGAGTGTTC[A/G]TGGTGACACACTCCT | 9100 |
| rs756912033 | snp | A/C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84710479 | GAGACAGATTAATGT[A/C/G]AGGCAGGTAGCCCTT | 9100 |
| rs756919470 | snp | C/G/T | 1.69083e-05 | 0.00290755 | intron-variant | USP10 | GRCh38.p7 | 16:84762939 | GCATGTCCTGCAGGC[C/G/T]TTTGACAGTGATCAG | 9100 |
| rs756946420 | in-del | -/AGAC | | | intron-variant | USP10 | GRCh38.p7 | 16:84749044 | TGTTGAGGCTTCGAT[-/AGAC]AGAACGTAGTTGTTG | 9100 |
| rs756948156 | in-del | -/GA | | | intron-variant | USP10 | GRCh38.p7 | 16:84770864 | CAAAGTCAAGAGATC[-/GA]GACCATCCTGGCCAA | 9100 |
| rs756961300 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84700920 | TCACATCTTCTCCCC[C/G]CTCCGCCATTATAAT | 9100 |
| rs756962973 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84754052 | TTACCTTAGATGGTG[C/T]GGACTTTGTTGAGCA | 9100 |
| rs757000259 | snp | A/G/T | 5.23358e-05 | 0.00511523 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745215 | GGCAGCCAGAGGGGG[A/G/T]CCCCGGGGCTGATTT | 9100 |
| rs757012164 | snp | A/G | 1.6571e-05 | 0.0028784 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84763032 | TAGGCTTCATTCTAA[A/G]TGGACTTCATGAGGA | 9100 |
| rs757025997 | in-del | -/TG | 0.000164116 | 0.0090571 | intron-variant | USP10 | GRCh38.p7 | 16:84768171 | GTCTCTTAATTTTTT[-/TG]TTTTTGCTTTCAATT | 9100 |
| rs757026075 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84765791 | AGACCCGTGACTGGG[A/C]TGGAGTCCCTGGGCA | 9100 |
| rs757035564 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84757842 | CCTTATTGGTGAAAG[C/G]GTCAAAGTGGTGGTA | 9100 |
| rs757054436 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84756883 | CTGTCAATAGACTTT[A/G]AGCCTGTGGGGAAAA | 9100 |
| rs757071995 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84739428 | AGGTGCCTGCCACCA[C/T]GCCCAGCTGATTTTT | 9100 |
| rs757073353 | snp | C/G | 1.66735e-05 | 0.00288729 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744878 | TCTAATGTGGAGGCG[C/G]AAGTTTTGGAAAATG | 9100 |
| rs757094866 | snp | C/T | 1.65696e-05 | 0.00287828 | intron-variant | USP10 | GRCh38.p7 | 16:84740304 | TTTTCTGATTCCTTG[C/T]GCAGCTTCCTCCATA | 9100 |
| rs757103337 | snp | C/G/T | 0.00134499 | 0.0258976 | intron-variant | USP10 | GRCh38.p7 | 16:84732571 | CCTGGCTCAGCCTCC[C/G/T]GAGCAGCCGGGACTA | 9100 |
| rs757127059 | snp | C/T | 3.40026e-05 | 0.00412312 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779098 | ACCCTGTGTGCGCTG[C/T]GTGTGCGCCCAGTGC | 9100 |
| rs757129174 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84731856 | TCCATTGCTTTGAGG[G/T]TTTCTTAGTGAAATT | 9100 |
| rs757148880 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84724596 | AAATTTTGCTATAGC[C/G]CTATTAGTGAGGGAA | 9100 |
| rs757197656 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84717072 | GTCTTGTGAATGTGC[A/T]CATTTAGATTCAGTA | 9100 |
| rs757198751 | in-del | -/GTGTGTGTGGTGTGG | | | intron-variant | USP10 | GRCh38.p7 | 16:84736725 | TGTTGGCAGTGGGCA[-/GTGTGTGTGGTGTGG]GTGTGTGTGGGTACT | 9100 |
| rs757201923 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84776717 | CTGGTCAGGGCCCCA[G/T]TGTGAGCACACACAC | 9100 |
| rs757201950 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84725125 | TTTGCAGCTAACACC[A/G]TAGTCCATTTTAGAA | 9100 |
| rs757230128 | snp | C/G | 2.95469e-05 | 0.00384351 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84768272 | TTGGATATCCAGTCA[C/G]ACAAGATACGCACAG | 9100 |
| rs757245251 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84704595 | TGGATGAAGAATTAG[C/T]GTAGGAAAATAAAGG | 9100 |
| rs757251475 | snp | A/G | 6.62833e-05 | 0.0057565 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84775177 | CTGCTTTCTCCAGGG[A/G]TTAAAAATAAGAATT | 9100 |
| rs757261050 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84707566 | ATAATATGGTCTGTT[A/G]TATCTAGTCACTGAA | 9100 |
| rs757285877 | snp | A/G | 5.36994e-05 | 0.00518139 | missense, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84778913 | TCTACCATCACGGCA[A/G]CAGTGCGACGGGCGG | 9100 |
| rs757302766 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84777804 | GTGCTGAAATTCCCT[A/G]CCAGCCAAGTCTTGC | 9100 |
| rs757303760 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84751672 | CAAGATAGTGTGTGT[G/T]CTTCCAAATTGATGG | 9100 |
| rs757340449 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84772429 | ATGAAGTCCTGCCAC[A/G]GGACTCTTGGGCCTC | 9100 |
| rs757343509 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84723612 | TCCTCTTCCTGAATT[C/T]ATTTGTTCAACAAAG | 9100 |
| rs757351924 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84733699 | ATTTACTTTATTAGG[C/T]TTTGAAAAGCAAATA | 9100 |
| rs757353712 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84744013 | AGAGAATTCAGAAGA[C/G]TGCTCTGAAGTGCGC | 9100 |
| rs757393868 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84759699 | AATATTTTAGCGTTT[A/C]CCAGCATATATCACT | 9100 |
| rs757406872 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84771555 | CAGTTTTATCAATAC[C/T]ATCAGAGTTATTTTA | 9100 |
| rs757418811 | snp | C/G | 3.55057e-05 | 0.00421326 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779124 | AGTGCCCGCTTCGTA[C/G]GACACCACCTCACAC | 9100 |
| rs757444995 | snp | A/C/T | 3.31358e-05 | 0.00407026 | synonymous-codon, stop-gained, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84759940 | GTACCTCCAAAACCC[A/C/T]GACAAGGTTAGTAAA | 9100 |
| rs757448572 | snp | A/G | 1.66565e-05 | 0.00288583 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744962 | CCACCTGGATATTAC[A/G]GCTATTTGAAAGATG | 9100 |
| rs757457054 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779733 | CATTAAAAGATTTCA[A/G]ATTGCATTCATGCTT | 9100 |
| rs757495385 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84749958 | ACGCCAGGGGAGAGC[A/G]TGTGAACTGAATACT | 9100 |
| rs757497403 | snp | C/T | 3.36298e-05 | 0.00410046 | intron-variant | USP10 | GRCh38.p7 | 16:84764297 | TAACTTAATATTTGC[C/T]TTTTCTAGGGTTTTG | 9100 |
| rs757512087 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84773107 | TCTAGTTGTGGTGGC[A/G]CACAAATAAGACGTG | 9100 |
| rs757533007 | snp | C/T | 1.66358e-05 | 0.00288402 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84745029 | ATGGCCATGCCAATT[C/T]AGCAGTCCCGAACAG | 9100 |
| rs757540298 | snp | C/T | | | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84716236 | AGACTGGAAGATTGT[C/T]CTTTCTCCTTGGCAA | 9100 |
| rs757541105 | snp | A/G | 0.000185787 | 0.00963634 | utr-variant-5-prime, intron-variant | USP10 | GRCh38.p7 | 16:84704815 | CTGCCATTCTGTCCC[A/G]TCTTGAAACATCATG | 9100 |
| rs757588067 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84754708 | AAGGTTTCTGTCTGA[C/G]TAGTTCATGCTGTCT | 9100 |
| rs757593306 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84740053 | GTCCATTGGAGTTCA[A/T]TTTTATTCCTTTTGG | 9100 |
| rs757617662 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84721954 | CTCACCTTGGCCTCC[C/G]AAAGTGCTGGAATTA | 9100 |
| rs757649598 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84748344 | GGTCTCACTCTGTCG[C/T]CCAGGCCGGAATGCA | 9100 |
| rs757655093 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84775372 | CGGGGAGTCACGTGA[C/G]AGTTTTACCTGAAAC | 9100 |
| rs757659799 | snp | A/G | 2.70325e-05 | 0.00367635 | intron-variant | USP10 | GRCh38.p7 | 16:84764050 | TTTGCTGTTCTTGTC[A/G]TAAATAGTAGTGTAA | 9100 |
| rs757708522 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84714704 | TTTATCTTATTTCCT[A/G]GAGCAAATTAAGCAC | 9100 |
| rs757713277 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84766698 | CGTCCATTTGGAGGA[C/G]TTGCTGGCTCAGATT | 9100 |
| rs757724420 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84740538 | ACTTTGACTAGTGAA[C/T]TGGTTTTAAAGCGTA | 9100 |
| rs757749121 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84722608 | ACTCTGTCTCCCAGG[C/T]TGGAGTGCAGTGGTG | 9100 |
| rs757817781 | snp | A/G | 1.67304e-05 | 0.00289222 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745362 | TACTTGAATCCTCGG[A/G]TGAGGGCACAGCTAC | 9100 |
| rs757843457 | in-del | -/TGGG | | | intron-variant | USP10 | GRCh38.p7 | 16:84757398 | AGGGAATGAGAGGGG[-/TGGG]GGTGTGTGTGTGTGT | 9100 |
| rs757853859 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84768915 | TTAAGAGTATCACAT[G/T]ATAGCTTGGTGGAGT | 9100 |
| rs757861738 | snp | A/G | 1.65759e-05 | 0.00287883 | intron-variant | USP10 | GRCh38.p7 | 16:84758823 | GTATCCTTCCTGGAC[A/G]CCGTCCGCAAGGCCA | 9100 |
| rs757869338 | snp | G/T | 3.35649e-05 | 0.0040965 | intron-variant | USP10 | GRCh38.p7 | 16:84759346 | TTCCTTTACGCTTCC[G/T]TACTGCCACTACATA | 9100 |
| rs757876314 | snp | A/G | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698182 | AAAGCTGAAATATAT[A/G]GCACTACTTAGAGCC | 9100 |
| rs757905790 | snp | C/G | 1.66963e-05 | 0.00288927 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745421 | AGCATAGACTTGGAC[C/G]CAACCAAACCCGAGA | 9100 |
| rs757906183 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84716696 | AATAATGAATAAATG[C/G]AGAGTTACTGGGATC | 9100 |
| rs757956579 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84749491 | CTGCCAGGCATGATA[C/G]TGTGGAGATTGAGGC | 9100 |
| rs757979387 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84743059 | CCGTTTCAATCTGGG[G/T]AGCCTTGACGGCCCC | 9100 |
| rs757993019 | snp | C/T | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699768 | CTCTACCTGCCTGCC[C/T]TCTCCCCTTCCGGAT | 9100 |
| rs757997894 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84760776 | AGACCAAGGGGCCAG[A/G]GAGCCCTTATAAAAG | 9100 |
| rs758011781 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84749926 | AAGTGTGAACTGTTA[C/T]TTGAAAGGAGAAGGA | 9100 |
| rs758033700 | snp | C/G | 1.67719e-05 | 0.0028958 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764117 | CGGCCCCAAAAACCA[C/G]TCGGTCAATGAAGAA | 9100 |
| rs758041475 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84717052 | CCGTTGAGAATCAGC[G/T]GCGGGTCTTGTGAAT | 9100 |
| rs758073692 | snp | A/C | 2.50812e-05 | 0.00354118 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84760239 | CACATATATTTACAG[A/C]CTCCTGACAGTTAAC | 9100 |
| rs758113593 | in-del | -/A | | | intron-variant | USP10 | GRCh38.p7 | 16:84704341 | TGTAATTAGGCTGTT[-/A]ACTTTTCTATTTACT | 9100 |
| rs758144610 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84709215 | GTACACGTCACTCCA[A/G]ACTGAGAGATGTTTC | 9100 |
| rs758154068 | snp | A/G | 3.34706e-05 | 0.00409074 | intron-variant | USP10 | GRCh38.p7 | 16:84772705 | TGCATACATAAGGTC[A/G]GGAGTGTTCGTGGTG | 9100 |
| rs758166025 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84763823 | CGTGGATCCAGTGAC[A/G]TTGTGCCTGTTGGGA | 9100 |
| rs758172538 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84737546 | ACAGTGCCACAACCC[A/T]TCTGGCATTCCTGCA | 9100 |
| rs758190121 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84705194 | GAGAGTATCCCTAAT[A/G]AAAAGGTGAGTGTCC | 9100 |
| rs758194569 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84708036 | TGAGTCGAGATTGTG[C/G]CACTGCACTTCAGCT | 9100 |
| rs758198904 | snp | G/T | | | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744813 | AAGAAGCAAGCTATG[G/T]CTCCATCGACTGCCA | 9100 |
| rs758221249 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84755987 | CAGTCAGTGAGAACC[G/T]TCTAGTATATCTGTT | 9100 |
| rs758239139 | snp | A/G/T | 5.23943e-05 | 0.00511809 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745211 | GCAGGGCAGCCAGAG[A/G/T]GGGGCCCCGGGGCTG | 9100 |
| rs758276095 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84723733 | AATCAGCTTTATGGA[A/G]GTATAACGTATGTGC | 9100 |
| rs758281003 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84731102 | CTCCTGCATCAGCCT[C/G]CTGAGTAGCTGGGAC | 9100 |
| rs758298591 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84704063 | AAGCCTAAGCGGCAC[C/G]TTGCACTGTGCTGTG | 9100 |
| rs758304284 | in-del | -/TGT | | | intron-variant | USP10 | GRCh38.p7 | 16:84748775 | ATAAATAGTTTGTTA[-/TGT]TCTGTATATGTTAAA | 9100 |
| rs758322140 | in-del | -/TT | | | intron-variant | USP10 | GRCh38.p7 | 16:84730978 | ATAGCATTTCTACCT[-/TT]TTTTTTTTTTTTTTT | 9100 |
| rs758331832 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84703456 | CCTCCACATTTTACA[G/T]GATGGAAAGTCTTGG | 9100 |
| rs758334091 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84731712 | CGTTCTGTTGAGTTT[C/T]TTAATTTAGTGATTT | 9100 |
| rs758382878 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84766636 | CAGAGGGTCAGCATA[C/T]TCAAAGATCCCAAAT | 9100 |
| rs758384375 | snp | A/G | 1.66037e-05 | 0.00288125 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84733464 | TTTTAGCCCTGATGA[A/G]TTCAATCAATTCTTT | 9100 |
| rs758409182 | snp | C/T | 0.000142116 | 0.0084284 | utr-variant-5-prime, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84700046 | CGGCGGGGGAAGCAG[C/T]GTGAGCAGCCGGAGG | 9100 |
| rs758435806 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84758996 | AGTCCATCTCCCTCT[A/G]AAAGAGAGGATATGT | 9100 |
| rs758474390 | snp | C/G | 1.66051e-05 | 0.00288137 | intron-variant | USP10 | GRCh38.p7 | 16:84733525 | CAAAACTTTGTTTTA[C/G]TGAGTCCGTGGGTAG | 9100 |
| rs758475739 | snp | A/G | 1.66988e-05 | 0.00288949 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744933 | AAAGGGAGCGTAAAA[A/G]GAAGAAAAAGCGGCC | 9100 |
| rs758529765 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84706136 | ATCCCTTCTGCTTCA[A/G]CTTCCTAAAGTACTG | 9100 |
| rs758543131 | snp | A/C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84714667 | GGTTTTTTTGGTCCA[A/C/G]TTTTTAGTTGTTACT | 9100 |
| rs758579714 | snp | G/T | 1.67666e-05 | 0.00289534 | intron-variant | USP10 | GRCh38.p7 | 16:84764282 | TGTGCTTTTCTGGAA[G/T]AACTTAATATTTGCC | 9100 |
| rs758591620 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84732812 | CTTGCCAGACTCACA[C/T]CCGTGCAGTTTAACC | 9100 |
| rs758627430 | snp | G/T | 1.65688e-05 | 0.00287821 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84759930 | TAATATGCCAGTACC[G/T]CCAAAACCCCGACAA | 9100 |
| rs758643121 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84725562 | CCTGCCACCATGCCC[A/G]GCTAATTTTTTTTTG | 9100 |
| rs758644776 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84733511 | CAGTTGAGGTAAGAC[A/C]AAACTTTGTTTTAGT | 9100 |
| rs758648403 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84721718 | TTTGTTTTGTTTTAG[A/G]GATTGAGTCTTGCTC | 9100 |
| rs758662393 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84731354 | GCACAGAGTAGCCAC[A/G]TTTCTACTATTGATA | 9100 |
| rs758676212 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84707366 | GGGTACATTTTAATA[A/T]AGTCGTTTATTTTAT | 9100 |
| rs758680958 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84736242 | CATATGCTTTTTCTC[C/T]GTTGTTAGGAGCTTG | 9100 |
| rs758687803 | snp | A/C/G | 0.00016571 | 0.00910105 | missense, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779020 | AACCAGTACCAGGTG[A/C/G]TGAAACCAACTGCTG | 9100 |
| rs758695991 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84726104 | TTCAGGGCTGATCTC[C/T]TATTTCTATCAGTCC | 9100 |
| rs758735804 | snp | C/G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84728430 | CTGCAACCTCTGCCT[C/G/T]CCCGGTTCAAGCGAT | 9100 |
| rs758744575 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84753022 | TTCAGGCTGGAGTGC[C/T]GTGGCATGATCATAG | 9100 |
| rs758797613 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84753805 | TGATCCTGTATTACT[G/T]TCTAATGAGAACTTA | 9100 |
| rs758825695 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84755941 | TGCTCATCTGTTGTA[C/T]TCCTCCTCTAGTTGG | 9100 |
| rs758858010 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84729738 | TTAAGGATTAAAATG[C/T]GATTCACGTGTATTT | 9100 |
| rs758865392 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84721230 | TGTTGTGTAGCACTG[A/G]GAGGTCTTTGGACCA | 9100 |
| rs758893486 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84729066 | GCTTCTGGAAGTGAC[A/G]AGATTACAAGCGTGA | 9100 |
| rs758902600 | snp | C/T | 9.14353e-05 | 0.00676086 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84778908 | AGTGGTCTACCATCA[C/T]GGCAACAGTGCGACG | 9100 |
| rs758913752 | snp | C/G | 1.71287e-05 | 0.00292644 | intron-variant | USP10 | GRCh38.p7 | 16:84759522 | GGGTTTTTCCCGTCT[C/G]ATAATTAGAATTGAA | 9100 |
| rs758948016 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84774059 | GTTCGAGACCAGCCT[G/T]ACCAACGTGGTGAAA | 9100 |
| rs758962742 | snp | A/G | 6.49077e-05 | 0.00569646 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84768256 | ATTTTTCACGTTGCA[A/G]TTGGATATCCAGTCA | 9100 |
| rs758980440 | snp | A/G | 0.000215605 | 0.0103806 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744774 | GTTGTACAGCTTCCA[A/G]AATAACCCCTGATGG | 9100 |
| rs759001212 | snp | C/T | 5.15991e-05 | 0.00507907 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764102 | ACTTACGATTTCCAA[C/T]GGCCCCAAAAACCAC | 9100 |
| rs759001311 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84765270 | TTGTGTGTGTGTGTG[C/T]GCACATGGCAAGAGC | 9100 |
| rs759006784 | snp | C/T | 1.71091e-05 | 0.00292476 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745300 | TGGGGCTCAGCCCTG[C/T]GTTGGTACCGATACT | 9100 |
| rs759006932 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84765880 | AAGGTTTTTCTTTAT[C/T]TACCTGAGAGCTTTT | 9100 |
| rs759022866 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84712805 | CCAGGTGACTGACCC[G/T]CACGTCACATATAAG | 9100 |
| rs759033829 | in-del | -/AAGTAATGA | 1.65987e-05 | 0.00288082 | cds-indel, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84763078 | GAAGCTTCTCTCACC[-/AAGTAATGA]AAGTAGGTTATGGTC | 9100 |
| rs759038616 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84774901 | CCTGTTTTTAAGGGG[C/T]CTCCCACAGGAGCAT | 9100 |
| rs759041098 | snp | A/G | 0.000115634 | 0.00760286 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745634 | GTCAAAGAAGGGCTT[A/G]TTCCGGTTTCAGAGG | 9100 |
| rs759066734 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84731664 | AATGTTGCCCCATTG[C/T]CTTCCATAGCCTTGT | 9100 |
| rs759069913 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84709408 | AGCTGGAGGGGAGGG[A/G]CAGACGCACCATCCA | 9100 |
| rs759077873 | snp | A/C | 1.65952e-05 | 0.00288051 | missense, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84778986 | GCTGCGCATCGATGA[A/C]CAGACAGTCAAGGTG | 9100 |
| rs759083476 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84764445 | CCCCCGTGGCTTATT[C/G]TCTCCCTGCTGGCGC | 9100 |
| rs759094932 | snp | A/C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84713402 | TGCGCCCTCCTTCAC[A/C/G]CTTGTCACCCTGTCT | 9100 |
| rs759096105 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84738972 | AACAGACTTTGGGAA[C/G]TGCTGCACCAGAATG | 9100 |
| rs759121759 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84724332 | AAGGAAATTTTAGCT[C/T]GGAATCTCCATGAAA | 9100 |
| rs759136375 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84756648 | GAGTCTTAAGGTTAG[G/T]TTTAAAAAAAAAAGT | 9100 |
| rs759160879 | in-del | -/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84770768 | AGAGCGAGACTCCGT[-/C]CCCCAAAAAAAAAAA | 9100 |
| rs759177735 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84703922 | TAAATTCCTCACTAA[A/T]GCAAAAGTTAGGACA | 9100 |
| rs759211146 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84757544 | AGCTTATTTTTGAGC[A/G]ATGCCTTAGATGGAT | 9100 |
| rs759225092 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84704439 | TGGGCCATTGGATTA[C/G]TGTCATTTGTCACTT | 9100 |
| rs759233603 | snp | A/G | 5.1839e-05 | 0.00509086 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84760195 | GATAAAATCGTGAGG[A/G]ATATTCGCCCTGGAG | 9100 |
| rs759250051 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84776945 | AGCCCCCCGAGTAGC[G/T]GGGATTACAGCTGTG | 9100 |
| rs759260836 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84751288 | TAATGCCACATTTCT[A/C]AGAACATATCCCCAT | 9100 |
| rs759267173 | snp | A/C | 1.65792e-05 | 0.00287912 | missense, nc-transcript-variant, intron-variant | USP10 | GRCh38.p7 | 16:84759459 | TGTACGTCAACACCC[A/C]TGATAGACAGCTTGT | 9100 |
| rs759277669 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84752182 | TCATTCTGGCATTTT[A/G]TGCCTTTTCTCACAC | 9100 |
| rs759331117 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780061 | ACCACCACTCAGGTT[A/G]TGCTTGTTTAGTATT | 9100 |
| rs759382380 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84759694 | TAGAAAATATTTTAG[C/T]GTTTACCAGCATATA | 9100 |
| rs759384270 | in-del | -/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84740843 | CTCAGGTCAACTCTT[-/C]ACCTCCTGGTCTGTT | 9100 |
| rs759401676 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84760914 | GATGCTTAGGGAAAT[G/T]TATTCAGAGAGAAAA | 9100 |
| rs759421675 | snp | A/G | 1.73093e-05 | 0.00294183 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745191 | TCGGCAGTGACACCA[A/G]GACTGCAGGGCAGCC | 9100 |
| rs759460360 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84735120 | CAACTTTGACCCCCC[A/G]CCCCGCCTCAGGGGG | 9100 |
| rs759477244 | snp | A/G | 1.66128e-05 | 0.00288204 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744836 | GACTGCCAGTACCCA[A/G]GCTCTGCCCTCGCTT | 9100 |
| rs759477983 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84700745 | AGTGACATCCCTTGC[A/G]CGAATCCATCCCAGC | 9100 |
| rs759511467 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84727373 | TAAGTTAATCTTCCA[G/T]AGGAGAGAAAACACT | 9100 |
| rs759526809 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84753674 | TTCTCAGGAGCTGTC[A/T]TTTAGACTTTCTGGA | 9100 |
| rs759538225 | in-del | -/GCAG | | | intron-variant | USP10 | GRCh38.p7 | 16:84769110 | ACTGGGGAGATGAAT[-/GCAG]GCTGATAATTATGGA | 9100 |
| rs759544600 | snp | A/G | | | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719952 | TATTTTCAACAGATA[A/G]TAATTTTGCAGCTTT | 9100 |
| rs759547689 | snp | A/G | 1.65844e-05 | 0.00287957 | intron-variant | USP10 | GRCh38.p7 | 16:84775146 | CTTCAAGCCATTGAT[A/G]TTTTGTTTTCCAGAA | 9100 |
| rs759555310 | in-del | -/CTTTTTTTT | | | intron-variant | USP10 | GRCh38.p7 | 16:84711719 | GTGAGGAAGGGCTAG[-/CTTTTTTTT]TTTTTTTTTTTTTTG | 9100 |
| rs759575330 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84773785 | GGAAACCTGGAATGC[C/T]GGCTAAGTCAAAGAA | 9100 |
| rs759622704 | in-del | -/TTTTTTTTTT | | | intron-variant | USP10 | GRCh38.p7 | 16:84711720 | TGAGGAAGGGCTAGC[-/TTTTTTTTTT]TTTTTTTTTTTTGTC | 9100 |
| rs759637715 | snp | C/T | 1.67041e-05 | 0.00288994 | intron-variant | USP10 | GRCh38.p7 | 16:84762985 | TTATATTTGACCTTT[C/T]CAGGGTCGACAAGAA | 9100 |
| rs759668676 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84728881 | TTGGCTCACTGCAGC[C/T]TCCGCCTTCCAGGTT | 9100 |
| rs759686844 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84757486 | TCATTTGATTAGTGC[C/T]GAAGTCTGGGATCTG | 9100 |
| rs759694457 | in-del | -/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84721835 | CTCGAGTAGCTGGGA[-/C]TACAGGCACACGCCG | 9100 |
| rs759710766 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84775044 | ATAGAGTGTTGTTTT[A/G]TTCCTGGTCTGACAG | 9100 |
| rs759721384 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84729627 | AACCCTTGGCACTGA[C/T]TTCTTAGCCCGTTCC | 9100 |
| rs759725649 | snp | A/C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84721823 | CTGCCTCAGCCTCTC[A/C/G]AGTAGCTGGGACTAC | 9100 |
| rs759730040 | snp | A/G | 1.6669e-05 | 0.00288691 | intron-variant | USP10 | GRCh38.p7 | 16:84772697 | AAAGGTAATGCATAC[A/G]TAAGGTCGGGAGTGT | 9100 |
| rs759734784 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84775286 | AAGGGGTTTACAGCT[C/G]GGCACAGGTTTGCTG | 9100 |
| rs759748557 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84775676 | TTGAGAGGGTGGGCC[C/T]GATTACACAAGCTCC | 9100 |
| rs759770279 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84747811 | ACCTCAAGTGATCTG[C/T]TCGCTTCAGCCTCCC | 9100 |
| rs759797962 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84701674 | ACAATTCAAGGTTGA[A/T]TGAAATGTTAATTAA | 9100 |
| rs759827735 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84714430 | CTTAGGCCATCCTCC[C/G]TCTTTAGCCTCCCAA | 9100 |
| rs759844278 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84705153 | CTCTATGGCTCAGGA[A/G]TCTCAAAACCAGTCC | 9100 |
| rs759860913 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84766450 | TGAGGTCCAGGTTGG[C/T]GCGCAGCAGCGAGGG | 9100 |
| rs759871029 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84777565 | CTCCGAAGTACGGGC[C/G]CCACAGTCTTGCTGT | 9100 |
| rs759875763 | snp | A/C | 1.66297e-05 | 0.0028835 | intron-variant | USP10 | GRCh38.p7 | 16:84740277 | TTTAACATTTTGTTG[A/C]ATTAAAATTTGTTTT | 9100 |
| rs759900887 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84761743 | TTGCTTGCGCAAACG[A/G]TTTAGGCAGAATCCC | 9100 |
| rs759907355 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84743088 | CCAGAACATCAGGGA[A/C]TAGGGGATGTATGGA | 9100 |
| rs759912503 | snp | C/T | 1.74455e-05 | 0.00295338 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779115 | TGTGCGCCCAGTGCC[C/T]GCTTCGTAGGACACC | 9100 |
| rs759933604 | snp | A/G | 4.65983e-05 | 0.0048267 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745647 | TTGTTCCGGTTTCAG[A/G]GGATCCTGTAGCCAT | 9100 |
| rs759953051 | snp | A/G | 0.000116353 | 0.00762648 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744990 | ATGGTGGCGATGATA[A/G]TATCTCCACAGAAGC | 9100 |
| rs759963593 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84749886 | TAGGTTATGTGTCAA[A/C]ATTTTGTTCCATTGG | 9100 |
| rs759975164 | in-del | -/GAGCGAAACTCCATCTCAAAAT | | | intron-variant | USP10 | GRCh38.p7 | 16:84703014 | AAAAAAAAAAAAAAA[-/GAGCGAAACTCCATCTCAAAAT]AAATAAAAAAGTTTA | 9100 |
| rs759990249 | snp | C/T | 3.34532e-05 | 0.00408968 | intron-variant | USP10 | GRCh38.p7 | 16:84700127 | GTAGCCGCCGGTCTG[C/T]GCCTTCGGCCGGAAG | 9100 |
| rs760015188 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84750554 | TACTTTGGAGTTGAC[A/G]AACATGTGACGTTTG | 9100 |
| rs760023854 | snp | C/G | 1.67038e-05 | 0.00288992 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744922 | TGGTCTTGGACAAAG[C/G]GAGCGTAAAAAGAAG | 9100 |
| rs760028733 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84748014 | TAAAAATCAGCCAGG[C/T]GTGGTGGCGGGCGCC | 9100 |
| rs760078895 | snp | C/G | | | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780026 | CCCTTCGATCAGCTC[C/G]ACGTGTTTGTGGAAG | 9100 |
| rs760105040 | snp | C/G | 1.69035e-05 | 0.00290714 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779088 | CCTGCTGTAAACCCT[C/G]TGTGCGCTGTGTGTG | 9100 |
| rs760118873 | in-del | -/AAG | | | intron-variant | USP10 | GRCh38.p7 | 16:84766166 | CAACAGGTGAATAAT[-/AAG]AACCTCAGAAACCTG | 9100 |
| rs760131835 | snp | A/G | 1.65825e-05 | 0.00287941 | intron-variant | USP10 | GRCh38.p7 | 16:84775268 | TTCATTAAAACACTG[A/G]TGAAGGGGTTTACAG | 9100 |
| rs760155822 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717934 | GATGGTCCCAGAAAT[G/T]TGGGATTCGTGATCA | 9100 |
| rs760168583 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84727287 | CCTGTGAAGTCAGAC[A/C]CAGCGTTATTTTCAT | 9100 |
| rs760179345 | snp | C/G/T | 8.32957e-05 | 0.00645304 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745401 | TGGAGTTGCACACCA[C/G/T]GGAAAGCATAGACTT | 9100 |
| rs760191446 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84770704 | GTGAACCTGGGAGGC[A/G]GAGCTTGCAGTGAGC | 9100 |
| rs760207504 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84737967 | CTGTGTATTTTTCCC[A/G]ATTGCTGGGGTTTTC | 9100 |
| rs760213485 | snp | A/G | 2.77998e-05 | 0.00372815 | intron-variant | USP10 | GRCh38.p7 | 16:84768367 | ACAAGAGGTATGTTC[A/G]CACTTGATTTTGAAC | 9100 |
| rs760237494 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84772899 | AAATAACTAAACTCT[A/G]TAATCTTACTAGATT | 9100 |
| rs760265379 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84749532 | ATAACTTGAGCCCGG[C/G]AGTTCGAGGCCAGCC | 9100 |
| rs760292819 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84773559 | ACTCAGACACTGTCT[C/G]TCCCAGGCCTGCACA | 9100 |
| rs760299771 | snp | C/T | 3.31428e-05 | 0.00407066 | intron-variant | USP10 | GRCh38.p7 | 16:84759981 | GTTGATGCTATTACA[C/T]ATTGGGAGTTATGGA | 9100 |
| rs760324183 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84715373 | GAAACAACTGGGCAC[A/G]TTACAAGATGTGTAA | 9100 |
| rs760341393 | snp | G/T | 6.62789e-05 | 0.00575631 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84759921 | TGAGTTCACTAATAT[G/T]CCAGTACCTCCAAAA | 9100 |
| rs760352695 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84767203 | TGTCCACACCCATTT[C/T]ATTCCGTTGAGAAAC | 9100 |
| rs760417798 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84730900 | CCTTAGGTATCTTCC[C/G]CACATTCTGAAGTAA | 9100 |
| rs760434627 | snp | G/T | 1.67055e-05 | 0.00289006 | intron-variant | USP10 | GRCh38.p7 | 16:84733409 | GTATATTTTATGTGA[G/T]CAGTGACTCTCTTAT | 9100 |
| rs760466486 | in-del | -/GA | | | intron-variant | USP10 | GRCh38.p7 | 16:84736016 | GACCTGTGGGTGTGT[-/GA]GTGGCGAGGGCGTGT | 9100 |
| rs760482229 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84759548 | TTGAAATAGTTTAGT[A/G]AAGCTCTTGATTTCC | 9100 |
| rs760516458 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84707217 | GCATAATCTTTCACA[C/G]TGTGACTTCCCCTTA | 9100 |
| rs760539726 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84768092 | CTTTTGAAAGTGATA[C/T]TGAATAATCTTATTT | 9100 |
| rs760556431 | snp | A/G | 3.31235e-05 | 0.00406948 | missense, nc-transcript-variant, intron-variant | USP10 | GRCh38.p7 | 16:84758799 | GGGAACTGGTGCTAC[A/G]TTAATGCTGTATCCT | 9100 |
| rs760558663 | snp | A/G | 0.00136023 | 0.0260435 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764160 | CAAGGTGAAGGAAGC[A/G]AGGATGAATGGGAAC | 9100 |
| rs760570006 | snp | A/C | 1.68128e-05 | 0.00289933 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745445 | CCCGAGAGTGCATCA[A/C]CTCCTGCTGACGGCA | 9100 |
| rs760621272 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84734119 | GCCCCTCTGTGGGCT[C/T]CTCCGGGACACAGAC | 9100 |
| rs760637755 | snp | C/G | 1.98647e-05 | 0.0031515 | intron-variant | USP10 | GRCh38.p7 | 16:84778891 | CTGCTGGGCTCTCTT[C/G]CAGTGGTCTACCATC | 9100 |
| rs760638751 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84761063 | TTTTAAATGCTTATA[A/G]TGCAGCTTTTGGTAT | 9100 |
| rs760643222 | snp | C/G | 1.65847e-05 | 0.0028796 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744765 | TTATTCTCGGTTGTA[C/G]AGCTTCCAAAATAAC | 9100 |
| rs760728944 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779608 | GCTGGTTCCTAACAG[C/G]AAAAATTTTAATAAT | 9100 |
| rs760762247 | snp | A/G | 1.65641e-05 | 0.00287781 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84772657 | TATCAAAAATATTGA[A/G]TATCCTGTGGACTTG | 9100 |
| rs760802094 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84747949 | CAAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 9100 |
| rs760819885 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84728795 | GTTTTATAAGCAGCA[C/T]CTCTTCTTTTTTCTT | 9100 |
| rs760830890 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84761662 | GTCCCATAGGTACCA[C/T]CTGCCTGGCTTGAAC | 9100 |
| rs760845652 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84736604 | CTGTTATTTATGTTC[A/G]GAAAGAAAGAGAAAA | 9100 |
| rs760859044 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84752799 | CCAGTTGATGGTTAT[C/T]GAAATGAGTCAGGAT | 9100 |
| rs760912022 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84753552 | AGCTCCTTACCTGTT[C/T]CAGGTGCGGAGTGAT | 9100 |
| rs760920763 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84728273 | TTTAGTTAAATAATT[A/G]TCACTCACTGGTATT | 9100 |
| rs760926702 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84731049 | CAGTGGCTCATTCTC[A/G]GCTTGCTGCAACCTC | 9100 |
| rs760936952 | snp | A/T | 1.70525e-05 | 0.00291992 | intron-variant | USP10 | GRCh38.p7 | 16:84759320 | TCAGGAAATGTGGTG[A/T]GTCTGTTCATTTCCT | 9100 |
| rs760956334 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84774341 | CAGCATGCCTCCGAC[A/G]GACTCTTGTGTCGGT | 9100 |
| rs760982706 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84775865 | GCCTTCCCTTTTATC[C/G]TTCTTTCTCTTTTAT | 9100 |
| rs761001264 | in-del | -/GTT | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84719097 | CGCCCGGCCAGTTTA[-/GTT]GTTGTTGTTGTTGTT | 9100 |
| rs761010590 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84737193 | GGGAGACTTCAGAAC[A/G]TGACCTTCCTATAGC | 9100 |
| rs761043215 | snp | G/T | 3.33517e-05 | 0.00408347 | intron-variant | USP10 | GRCh38.p7 | 16:84740259 | TAAATGGTAAGCGTT[G/T]GTTTTAACATTTTGT | 9100 |
| rs761093626 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84756533 | AGGACACAGAGGTTG[C/T]AGTGAGCCAAGATTG | 9100 |
| rs761103695 | snp | C/T | 1.65734e-05 | 0.00287862 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745638 | AAGAAGGGCTTGTTC[C/T]GGTTTCAGAGGATCC | 9100 |
| rs761110563 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84716947 | CCAGAGCCATAGGGA[A/C]AGTCACTGTGATAGC | 9100 |
| rs761128390 | snp | C/T | 1.67716e-05 | 0.00289578 | missense, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779078 | GCCGAGTGGACCTGC[C/T]GTAAACCCTGTGTGC | 9100 |
| rs761140141 | in-del | -/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84723876 | TTGAGCCCCCTTGCA[-/G]CCTCTTCTTTTGTTC | 9100 |
| rs761141060 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84769351 | GGACTGGTTCACCCA[C/G]GCTCTGGGGGGATCA | 9100 |
| rs761144590 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84749379 | AGTTTGACTTGCATT[A/T]GTATCTAACTGTTTC | 9100 |
| rs761173636 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84763666 | TTTATGTAAACAAGG[A/T]TCCAGTGGTGGTGCA | 9100 |
| rs761178290 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84731630 | TAGGAACAAAATCCT[G/T]TTTTCTCGAAACTTT | 9100 |
| rs761226081 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84777388 | CTCTTAGCCCAGTCA[A/G]TTAGGTCTGTGAGGT | 9100 |
| rs761231755 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84724125 | CAGGAAGTTATTCAA[C/T]AATGAGGGCTATCTA | 9100 |
| rs761278030 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779180 | TCTTTAGAGAGAAAC[G/T]CTTTCTCCCTTTGCA | 9100 |
| rs761298255 | snp | A/T | 3.36185e-05 | 0.00409977 | intron-variant | USP10 | GRCh38.p7 | 16:84762972 | CACAGTAACGTGATT[A/T]TATTTGACCTTTTCA | 9100 |
| rs761298434 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84734031 | TTACATATTTTCCTG[G/T]CGAGGGCCATTTAGG | 9100 |
| rs761323188 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84743767 | AAATACGTCTGTCTT[A/G]GCAGGAATGAATTAT | 9100 |
| rs761354026 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84707002 | TAGAAAGTGCCTTAG[C/T]TTGTTTGAGCCTTTA | 9100 |
| rs761360580 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84778563 | CATCCAAGGGCATGA[A/G]CCAGGTCTGTAGGCC | 9100 |
| rs761373742 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84750748 | TTTTAACAGAATATA[A/G]ATAATGCTGGGTAAG | 9100 |
| rs761416121 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779252 | CACAACACAGCTTCT[G/T]TTGACTCTAACTTCC | 9100 |
| rs761500673 | snp | G/T | 1.6638e-05 | 0.00288422 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764242 | AGACTCCAATCACCG[G/T]CATTTTTGGTGGACA | 9100 |
| rs761502779 | snp | A/G | 1.66054e-05 | 0.00288139 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744689 | ATTGAACCCAGTGAC[A/G]CTTTGCCGAGAACCC | 9100 |
| rs761533606 | snp | A/G/T | 5.01143e-05 | 0.0050055 | intron-variant | USP10 | GRCh38.p7 | 16:84763118 | ACTTGCCGCAGAGTT[A/G/T]TGCAAGAGTTCGCTG | 9100 |
| rs761535129 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84744388 | TATTTTAATTTCTAC[C/G]TTCTGAAAGCCTTCC | 9100 |
| rs761547119 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84701513 | TGCTTTTTTCTCAAC[G/T]TAAATCCTAATTAAC | 9100 |
| rs761562249 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84739938 | AAGAGTCATCTTCGC[C/T]AGTGCACAAACAAAA | 9100 |
| rs761565041 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84737236 | TATCCTTTTCACAAG[A/G]CCGCAGCACTGTTTT | 9100 |
| rs761576896 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84749594 | AAAAAAAAAATTATA[C/G]ACACACAAAATGCTT | 9100 |
| rs761580541 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84721776 | GATCACAGCTCACTG[C/T]AACCTCCGCCTCCCG | 9100 |
| rs761586499 | snp | A/C | 6.74388e-05 | 0.00580645 | intron-variant | USP10 | GRCh38.p7 | 16:84772723 | AGTGTTCGTGGTGAC[A/C]CACTCCTGCACATCA | 9100 |
| rs761609673 | snp | C/T | 5.63857e-05 | 0.00530939 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84700105 | CATGGCCCTCCACAG[C/T]CCGCAGGTAGCCGCC | 9100 |
| rs761626417 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84766287 | CTTCTGTGTTCTGCA[C/T]TGTGAGCTCTATTCC | 9100 |
| rs761658807 | in-del | -/ATTTT | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698259 | TTATGTGTGTACATG[-/ATTTT]ATCTTTTGTTGAACC | 9100 |
| rs761679774 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84767113 | TAAAGGAGCATGGAG[A/T]TGCGTAATTAAACCC | 9100 |
| rs761683578 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84754284 | GTTTATGAAAGACTT[A/G]CCACTAGATAAAATT | 9100 |
| rs761696284 | snp | C/T | 1.69132e-05 | 0.00290797 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745318 | TGGTACCGATACTAC[C/T]GAAAACCTTGGAGTT | 9100 |
| rs761697625 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84746885 | TTAGCTTAAAACACA[C/T]ACTACAGCTATACAA | 9100 |
| rs761718280 | snp | A/G | 2.29318e-05 | 0.00338606 | intron-variant | USP10 | GRCh38.p7 | 16:84778874 | TGTTCTCACTCTGCT[A/G]CCTGCTGGGCTCTCT | 9100 |
| rs761731965 | snp | C/T | | | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84716449 | TCTTTATTAGATTCT[C/T]AGTATTGTGCTTCAG | 9100 |
| rs761751012 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84747702 | CCAAGTAGCTGGGAT[G/T]ACAGGCACATGCCAC | 9100 |
| rs761784210 | snp | A/G | 1.66879e-05 | 0.00288855 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745382 | GGCACAGCTACCAAC[A/G]GGGTGGAGTTGCACA | 9100 |
| rs761851913 | snp | A/G | 1.6588e-05 | 0.00287988 | intron-variant | USP10 | GRCh38.p7 | 16:84744594 | GTACTTAGAGTTTGT[A/G]GAACTGGGTTCTTAA | 9100 |
| rs761873538 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84715215 | GATTACAGGCGTGAG[A/G]CACCACTCCCGGCCC | 9100 |
| rs761884764 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84724036 | TTGAACTTCTACTAG[G/T]GCTATCCCAGATAAA | 9100 |
| rs761886181 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84719020 | TGGTCTCGAACTCCT[C/G]ACCTCAAATGATCCA | 9100 |
| rs761893248 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84726756 | AATAGCTTCTCTAGT[C/T]CACAGTCTTACTTCC | 9100 |
| rs761907904 | snp | A/T | 3.32452e-05 | 0.00407695 | intron-variant | USP10 | GRCh38.p7 | 16:84758673 | TTGAATGTTCTTCAC[A/T]AGATGTCATCAATTT | 9100 |
| rs761935673 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84776783 | CCTGGGCCTGGGTTG[C/T]TCTCCCCTGCCCTCC | 9100 |
| rs761957313 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84763459 | TATACATACATACGC[A/G]TACATTTTCCCTGAA | 9100 |
| rs761958782 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84735970 | TGTGGTTGGGCCTGT[A/G]GGTGTGTGAGTGGCG | 9100 |
| rs761965616 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84768526 | ATGAAATGGTTGAAA[C/T]GTGATCCCAAGGGCC | 9100 |
| rs761984266 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84742356 | ATCCTTTTTCTAAAG[C/G]TATTCACAGCTTTCT | 9100 |
| rs761988726 | snp | A/G/T | 6.7386e-05 | 0.00580425 | intron-variant | USP10 | GRCh38.p7 | 16:84768395 | AACCTTTCTACTAAG[A/G/T]TGCTCTGGTTTGGTG | 9100 |
| rs762018503 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84769203 | AGGTAAAATAAGGTG[A/C]CCCAACGTAGAAGAC | 9100 |
| rs762045216 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84761651 | ACTGAGGGCTGGTCC[C/T]ATAGGTACCATCTGC | 9100 |
| rs762059896 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84708893 | GTGGCCGGACGTTAG[A/G]AGTATAGAGCTGAAG | 9100 |
| rs762060650 | snp | C/G | 2.01465e-05 | 0.00317377 | intron-variant | USP10 | GRCh38.p7 | 16:84764078 | TAAGCAGATGCTCTC[C/G]TTTTCAGAACTTACG | 9100 |
| rs762064034 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780122 | AGTTTTTGACTCTTC[A/G]ATTGGCAGAAAGGAG | 9100 |
| rs762071614 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84760998 | AAGAAGAGTGAATGT[C/T]GAGGGCATCGTTGCA | 9100 |
| rs762080710 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84716900 | TGCCTCTAATTTGGA[A/T]GATAAATGGTTACGC | 9100 |
| rs762104319 | in-del | -/ACTC | | | intron-variant | USP10 | GRCh38.p7 | 16:84749651 | AAGTTTGTTTCAAAT[-/ACTC]ACATTTCTGGACTAT | 9100 |
| rs762105904 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84764291 | CTGGAATAACTTAAT[A/G]TTTGCCTTTTCTAGG | 9100 |
| rs762143067 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84727597 | CCTGTTGTTAAGATT[A/C]AATCCATTTGCTTAA | 9100 |
| rs762146698 | in-del | -/T | 0.165637 | 0.235336 | intron-variant | USP10 | GRCh38.p7 | 16:84732445 | GACTTCTTCTTCTTC[-/T]TTTTTTTTTTTTTCT | 9100 |
| rs762153766 | snp | C/G | 1.65614e-05 | 0.00287757 | missense, nc-transcript-variant, intron-variant | USP10 | GRCh38.p7 | 16:84758777 | ACCCCGTGGGCTGAT[C/G]AATAAAGGGAACTGG | 9100 |
| rs762159323 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84756379 | AGGTGGATCACTTGA[A/G]CTCAGGAGTTCAAGA | 9100 |
| rs762175594 | snp | A/G | 0.000224005 | 0.0105807 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745169 | GACAGTCCTTTCCCC[A/G]GAGCACTCGGCAGTG | 9100 |
| rs762190457 | in-del | -/TT/TTT | | | intron-variant | USP10 | GRCh38.p7 | 16:84747554 | TTTAAAGCCAGGTGA[-/TT/TTT]TTTTTTTTTTTTTTT | 9100 |
| rs762207991 | snp | C/T | 1.65638e-05 | 0.00287778 | intron-variant | USP10 | GRCh38.p7 | 16:84772538 | GTGTGCTTTGTGTCT[C/T]AGGTTGAGATAAGTC | 9100 |
| rs762214396 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84712720 | TGCATTTAGAATGCA[G/T]GAGTGACCCCTAAGC | 9100 |
| rs762219928 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84751088 | TACGACAGTGGTCCC[A/G]TAAGATTATAATGGA | 9100 |
| rs762270766 | snp | A/T | 5.00129e-05 | 0.0050004 | intron-variant | USP10 | GRCh38.p7 | 16:84733419 | TGTGATCAGTGACTC[A/T]CTTATTTTTTTTCAG | 9100 |
| rs762280236 | snp | A/G | 3.44525e-05 | 0.00415031 | intron-variant | USP10 | GRCh38.p7 | 16:84760283 | CTGAAAAGGTTTGAG[A/G]CTTCTCTGTTGTCAC | 9100 |
| rs762282378 | snp | C/G | 1.70017e-05 | 0.00291558 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745467 | CTGACGGCACGGGCT[C/G]TGCATCAGGCACCCT | 9100 |
| rs762292607 | in-del | -/CA | | | intron-variant | USP10 | GRCh38.p7 | 16:84755795 | AGAGTGAGACTGTCT[-/CA]AAAAAAAAAAAAAAA | 9100 |
| rs762296294 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84775678 | GAGAGGGTGGGCCCG[A/C]TTACACAAGCTCCTC | 9100 |
| rs762329249 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84729865 | ATAGTTCAGTGTTGC[A/G]TAGCTGGTAATCAGC | 9100 |
| rs762339197 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84766240 | GTGGATTTAGAAGCC[A/G]GTTGAGCAGCCATGT | 9100 |
| rs762374652 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84703221 | GGTCCAAGTGAATAT[C/G]CTTGTCACTGAGGGG | 9100 |
| rs762387378 | snp | C/T | 1.66635e-05 | 0.00288643 | stop-gained, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779065 | CTCCTGTATTACCGC[C/T]GAGTGGACCTGCTGT | 9100 |
| rs762389091 | in-del | -/CAGTAA | 1.65526e-05 | 0.00287681 | intron-variant | USP10 | GRCh38.p7 | 16:84759507 | TGTGTTAAGTGGTGG[-/CAGTAA]GGTTTTTCCCGTCTG | 9100 |
| rs762462772 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84704496 | TCATTTCCAGAGACT[C/T]GTATGTGCTTGGACT | 9100 |
| rs762465122 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84710913 | TTGTTGAGCCCTTTC[G/T]CATGAATAGCAATAA | 9100 |
| rs762475437 | snp | A/C | 3.32541e-05 | 0.00407749 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764237 | TGTTCAGACTCCAAT[A/C]ACCGGCATTTTTGGT | 9100 |
| rs762478623 | snp | A/G | 2.49822e-05 | 0.00353419 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84760202 | TCGTGAGGGATATTC[A/G]CCCTGGAGCTGCCTT | 9100 |
| rs762486049 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84724958 | AACTTACTGGGCTTT[C/G]ATTCATAAAGCCTAG | 9100 |
| rs762494682 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84714088 | ACAGCTCTGTGGTGG[C/G]CACATGCAGTTTGGA | 9100 |
| rs762495504 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84737336 | GGGAATTTTATGTCT[C/T]TGCTTTGATTTTTGA | 9100 |
| rs762531160 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717405 | GCATAATGGACATTC[A/T]GTACACACTAGCTGT | 9100 |
| rs762553678 | snp | C/T | 3.32546e-05 | 0.00407752 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744846 | ACCCAGGCTCTGCCC[C/T]CGCTTTGGATGGAAG | 9100 |
| rs762565536 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84733193 | TACAAAATTGATTTG[C/T]TTCAAAATAAGCTTT | 9100 |
| rs762620253 | snp | C/T | | | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719514 | TGAGGATGCTCTGAT[C/T]CTAAGGTGTGGCCAG | 9100 |
| rs762635337 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84750575 | GTGACGTTTGAAATT[A/G]AACGTATGCTTTCAT | 9100 |
| rs762659559 | snp | A/C | 1.69381e-05 | 0.00291011 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745314 | GCGTTGGTACCGATA[A/C]TACTGAAAACCTTGG | 9100 |
| rs762674790 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779911 | AATAAAAATCACAAA[-/G]GTTGGTTTAAAGGTG | 9100 |
| rs762682987 | snp | C/G | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698928 | CATCCCATTTATGAA[C/G]AGACCAGGCTCCCTA | 9100 |
| rs762688163 | snp | C/G | 4.97409e-05 | 0.00498678 | intron-variant | USP10 | GRCh38.p7 | 16:84775156 | TTGATATTTTGTTTT[C/G]CAGAACTGCTTTCTC | 9100 |
| rs762736304 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84778495 | ATGACATCATAATCT[C/G]TGTCCAAGATTCAGA | 9100 |
| rs762742134 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84774309 | CATGGGTCAGAAGTA[C/T]AGATGGCTGCCTCGA | 9100 |
| rs762810526 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779513 | TACCCTTTAGTTTTT[C/G]ATAAATGATAAAAAT | 9100 |
| rs762826067 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84739362 | CTGCAACCTCCATCC[A/C]CCAGGTTCAAACGAT | 9100 |
| rs762854981 | snp | A/T | 1.66043e-05 | 0.00288129 | intron-variant | USP10 | GRCh38.p7 | 16:84740285 | TTTGTTGAATTAAAA[A/T]TTGTTTTCTGATTCC | 9100 |
| rs762958912 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84720775 | TTTTAATAGAGACGG[C/G]GTTTCACCGTATTAG | 9100 |
| rs762960741 | in-del | -/GGGGTG | | | intron-variant | USP10 | GRCh38.p7 | 16:84757394 | AAGGAGGGAATGAGA[-/GGGGTG]GGGGTGTGTGTGTGT | 9100 |
| rs762964377 | in-del | -/CGTGAA | | | intron-variant | USP10 | GRCh38.p7 | 16:84748069 | GAGACAGGAGAATGG[-/CGTGAA]CGTGAACCTGGGAGG | 9100 |
| rs763006705 | snp | C/T | 1.72442e-05 | 0.00293629 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745269 | AGGCTGGCAGAGACA[C/T]CCTGTCAAGGACAGC | 9100 |
| rs763034830 | snp | A/G | 1.68329e-05 | 0.00290106 | intron-variant | USP10 | GRCh38.p7 | 16:84745722 | ATGGGAGCAGACCTC[A/G]TCAACTGGGCTTATA | 9100 |
| rs763067345 | snp | A/G | 1.658e-05 | 0.00287919 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84763008 | GACAAGAAGATGCTG[A/G]GGAATACTTAGGCTT | 9100 |
| rs763074703 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84703171 | CTCAGCATTTTAGCA[A/G]AGACAAATAAATGAA | 9100 |
| rs763078994 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84775316 | GCAACTTAGCATAGC[A/G]ACCAGATGCTGTACT | 9100 |
| rs763116038 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84759814 | ATAGCTGATATTCTA[C/T]TTAGCCATCAAAGCT | 9100 |
| rs763132081 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84767235 | AGGTCACCGAGACTG[C/T]AGAAATAGAAGCCCT | 9100 |
| rs763132865 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84748596 | GGCGTGAGCCACCGC[A/G]CCCAGCTGAGAATAT | 9100 |
| rs763135802 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84723086 | CAAAGATGGGGGGTG[G/T]GGAATAAAGTCGATT | 9100 |
| rs763135823 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84715505 | CCTCCCAAAGTGCTG[A/G]GATTACAGGCATGAG | 9100 |
| rs763163827 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84730500 | ATAATTAAGTAAAAC[C/T]AATAAATTTGAAAAT | 9100 |
| rs763183802 | in-del | -/TTTCTTTTCTC | | | intron-variant | USP10 | GRCh38.p7 | 16:84735512 | CTTTTGGGCCTCCCA[-/TTTCTTTTCTC]TTTCTTTTGTTTTTT | 9100 |
| rs763190933 | snp | C/T | | | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84716267 | ATCATCTGTACTATC[C/T]GATTGCATCTTACAG | 9100 |
| rs763227325 | snp | A/T | 4.97434e-05 | 0.00498691 | intron-variant | USP10 | GRCh38.p7 | 16:84740412 | GAAGGGAATTTGGCC[A/T]TACGTGCTGGGTGGG | 9100 |
| rs763230809 | snp | A/C/G/T | 0.000417233 | 0.014438 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745653 | CGGTTTCAGAGGATC[A/C/G/T]TGTAGCCATAAAGAT | 9100 |
| rs763305384 | snp | C/T | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698910 | CACTTATATTTTTCA[C/T]GGCATCCCATTTATG | 9100 |
| rs763321860 | in-del | -/TTG | | | intron-variant | USP10 | GRCh38.p7 | 16:84701459 | TTGGTGTATTTAGCT[-/TTG]TTTAGACCTTTCTGT | 9100 |
| rs763327058 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84737149 | GGAGAGTCTTTGAGA[C/T]GGAAAGCAGAACACA | 9100 |
| rs763342269 | snp | C/T | 5.83618e-05 | 0.00540162 | intron-variant | USP10 | GRCh38.p7 | 16:84768375 | TATGTTCACACTTGA[C/T]TTTGAACCTTTCTAC | 9100 |
| rs763366931 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84748302 | AGTCATGAGAATTTT[A/C]TTTTCTTTTCTTTAT | 9100 |
| rs763374755 | in-del | -/GTTCAACAACAAAATGATGATG | 1.65701e-05 | 0.00287833 | intron-variant | USP10 | GRCh38.p7 | 16:84759975 | GTTTTGTTGATGCTA[-/GTTCAACAACAAAATGATGATG]TTACATATTGGGAGT | 9100 |
| rs763395671 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84754471 | TACATTTCCTAGTAC[A/G]CGTCCCAAGGGCCCG | 9100 |
| rs763403912 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84743215 | AGGAATTAGATGGTC[A/G]TGACTTCATGCATAA | 9100 |
| rs763407219 | snp | A/C | 0.00035317 | 0.0132838 | intron-variant | USP10 | GRCh38.p7 | 16:84732520 | GGCGCGATCTCAGCT[A/C]ACTGCAACCTCGGCC | 9100 |
| rs763411564 | snp | A/T | 1.66217e-05 | 0.0028828 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84745000 | TGATAGTATCTCCAC[A/T]GAAGCCCTGGTCAAT | 9100 |
| rs763420937 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84736782 | AGAGTAGAGACAGTT[C/T]TTAATTTGGTGTGTT | 9100 |
| rs763436759 | snp | C/T | 4.97162e-05 | 0.00498554 | intron-variant | USP10 | GRCh38.p7 | 16:84772519 | ACAGGGACGGTGTGT[C/T]CTGGTGTGCTTTGTG | 9100 |
| rs763459041 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84743711 | TTGAAAGACACAATT[A/G]ATTCTAAAACTTAAC | 9100 |
| rs763472070 | snp | A/G | | | intron-variant, splice-donor-variant | USP10 | GRCh38.p7 | 16:84733106 | TGAGTCAGCAGAAAG[A/G]TAAATGGAACAACTG | 9100 |
| rs763536741 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84710988 | AGGCGTGAACAACAA[C/T]AAAAATATGAATTGT | 9100 |
| rs763538257 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84777603 | CTGTTCAGTCTCCTC[C/T]GGGGTCCCTGCACAG | 9100 |
| rs763577101 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84732533 | CTCACTGCAACCTCG[G/T]CCTCCCTGGTTCAAG | 9100 |
| rs763620909 | snp | A/G | 1.67624e-05 | 0.00289498 | intron-variant | USP10 | GRCh38.p7 | 16:84759348 | CCTTTACGCTTCCTT[A/G]CTGCCACTACATAGA | 9100 |
| rs763620944 | snp | A/G | 1.65611e-05 | 0.00287755 | synonymous-codon, nc-transcript-variant, intron-variant | USP10 | GRCh38.p7 | 16:84758783 | TGGGCTGATCAATAA[A/G]GGGAACTGGTGCTAC | 9100 |
| rs763627921 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84725029 | TTTTTTAAAACTTTA[C/T]TGAGATATAATTCAC | 9100 |
| rs763644191 | snp | C/G | 1.66435e-05 | 0.0028847 | intron-variant | USP10 | GRCh38.p7 | 16:84759484 | GCTTGTAAGTAAGGT[C/G]GTGAAAGATGTGTTA | 9100 |
| rs763677569 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84772087 | GACAAGATCTCGCTG[C/T]GTTGCCCAGGCTGGG | 9100 |
| rs763693732 | in-del | -/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84736682 | CATCCCAACCATGAC[-/G]TGAGTCAATAAGCCC | 9100 |
| rs763701709 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84742562 | TGCTGTGTTAGGATT[C/T]GTGGTTTTAAGAGCC | 9100 |
| rs763715019 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84705641 | TTTTGTTTTCCCATT[A/T]GTCTTTGTTTTATGA | 9100 |
| rs763754218 | snp | A/T | 1.65762e-05 | 0.00287886 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764198 | CCCCCGGAACAAGAC[A/T]TCCGTCACCCGCCAG | 9100 |
| rs763762730 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84761921 | TTGCCCTTTTCTGCA[C/T]ACGTGCAGAGCATGC | 9100 |
| rs763790768 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84777521 | GCACAGGATGAAGCT[A/G]TGCCCTTGGATTGGC | 9100 |
| rs763824477 | snp | A/G/T | 5.02099e-05 | 0.00501027 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779076 | CCGCCGAGTGGACCT[A/G/T]CTGTAAACCCTGTGT | 9100 |
| rs763835263 | snp | C/G/T | 6.65075e-05 | 0.00576628 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744847 | CCCAGGCTCTGCCCT[C/G/T]GCTTTGGATGGAAGT | 9100 |
| rs763890062 | snp | A/G | 5.07687e-05 | 0.00503803 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745316 | GTTGGTACCGATACT[A/G]CTGAAAACCTTGGAG | 9100 |
| rs763895974 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84764629 | TGAGGTTAGAAGTTC[A/G]AGATCAACCTGATCA | 9100 |
| rs763914753 | snp | C/T | 1.6593e-05 | 0.00288031 | intron-variant | USP10 | GRCh38.p7 | 16:84740290 | TGAATTAAAATTTGT[C/T]TTCTGATTCCTTGTG | 9100 |
| rs763933948 | snp | C/G | 1.72421e-05 | 0.00293611 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745270 | GGCTGGCAGAGACAC[C/G]CTGTCAAGGACAGCT | 9100 |
| rs763935627 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84765623 | TATTACAGCTGAATA[C/G]TGTTCCCTTGTCTAT | 9100 |
| rs763960593 | snp | A/G | 1.67379e-05 | 0.00289287 | intron-variant | USP10 | GRCh38.p7 | 16:84772707 | CATACATAAGGTCGG[A/G]AGTGTTCGTGGTGAC | 9100 |
| rs763965445 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84739363 | TGCAACCTCCATCCC[A/C]CAGGTTCAAACGATT | 9100 |
| rs763986578 | in-del | -/TCTT | | | intron-variant | USP10 | GRCh38.p7 | 16:84746854 | TCTAAACTTTTTGAC[-/TCTT]TCATGAGAACATTTA | 9100 |
| rs763989088 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84757767 | GTTGAGGCCCTGGCT[A/C]TGCTACCTGGCTCCT | 9100 |
| rs764040107 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84748614 | CAGCTGAGAATATTA[C/T]AGTTTCGTTTCTAAA | 9100 |
| rs764042692 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84709728 | GCAAAGCTGGGAAGA[C/T]GTCTCTTGTAGAACG | 9100 |
| rs764058724 | snp | A/G | 8.8248e-05 | 0.006642 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779121 | CCCAGTGCCCGCTTC[A/G]TAGGACACCACCTCA | 9100 |
| rs764069286 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84766266 | CATGTGACCTTGAAC[A/C]AGTCACTTCTGTGTT | 9100 |
| rs764074351 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84713561 | AGGGCAGGGGTTTTT[C/G]TTTGCTTTGTTCACT | 9100 |
| rs764113091 | snp | C/T | 1.66471e-05 | 0.00288501 | intron-variant | USP10 | GRCh38.p7 | 16:84758667 | AATGATTTGAATGTT[C/T]TTCACTAGATGTCAT | 9100 |
| rs764115372 | in-del | -/A | | | intron-variant | USP10 | GRCh38.p7 | 16:84722342 | CTCTTTCCTCTTGAT[-/A]AGACATTTTTGTTGT | 9100 |
| rs764116954 | snp | A/G | 1.67019e-05 | 0.00288975 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744934 | AAGGGAGCGTAAAAA[A/G]AAGAAAAAGCGGCCA | 9100 |
| rs764129594 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84714240 | GGCGGGAGCCAGCTC[A/G]TTGTGGTTTGTTCAT | 9100 |
| rs764171658 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84707482 | CTCTGATCCTTAATC[A/G]TCAGTTTGGTGTGTG | 9100 |
| rs764185302 | snp | C/T | | | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84759920 | ATGAGTTCACTAATA[C/T]GCCAGTACCTCCAAA | 9100 |
| rs764193483 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84740507 | TGTAAACTGTAATGT[A/G]TTTAATTGCTGAATC | 9100 |
| rs764200312 | snp | A/G | 3.32452e-05 | 0.00407695 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84745009 | CTCCACAGAAGCCCT[A/G]GTCAATGGCCATGCC | 9100 |
| rs764215262 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84767272 | ACCCCTGGAATGTTT[C/T]CTTGCTGAGGCTAAA | 9100 |
| rs764247633 | snp | C/T | | | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84716276 | ACTATCTGATTGCAT[C/T]TTACAGTCTTCTTTA | 9100 |
| rs764290699 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84724983 | GCCTAGTAAAGAAAT[C/T]AAAATTTTTATTTTG | 9100 |
| rs764304762 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84708064 | GCTTGGGTGACAGAG[C/T]GAGACTCTTACGTCA | 9100 |
| rs764331152 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779709 | GATGGGTGATTGTAA[C/T]TTTATTGCCATTAAA | 9100 |
| rs764332756 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84736820 | TTGAGAGGGAGTCTC[A/G]CTCTCTCGCCCAGGC | 9100 |
| rs764336181 | snp | C/T | 3.21973e-05 | 0.00401218 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84768257 | TTTTTCACGTTGCAG[C/T]TGGATATCCAGTCAG | 9100 |
| rs764376385 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84762813 | TTTCTCCTTTTCCTC[C/T]TACTCTTGGGATTTC | 9100 |
| rs764381760 | in-del | -/CACTCCTACACGCTGCCCC | | | intron-variant | USP10 | GRCh38.p7 | 16:84755437 | TGCACTTGCTGTCTT[-/CACTCCTACACGCTGCCCC]CACTCCTACACGCTG | 9100 |
| rs764384195 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84729123 | TTGTCTTTTGGAATA[A/G]TGTTGATAATAAATG | 9100 |
| rs764405190 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84749327 | CTGAGTGAAAGTCTA[A/G]TTTCATTAAAAGATC | 9100 |
| rs764414801 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84710992 | GTGAACAACAACAAA[A/G]ATATGAATTGTGCCC | 9100 |
| rs764437778 | in-del | -/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84713948 | CGGGGCTGCAGCACT[-/G]GGGGTTGGCTGGGAA | 9100 |
| rs764442112 | snp | A/G | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698953 | TCCCTATTTTATGTA[A/G]CGTGGGAATGGATCT | 9100 |
| rs764483588 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84731579 | TGCACTTGAAAAGTA[A/G]TTTATAGAATTCTAT | 9100 |
| rs764517867 | snp | A/G | 0.000111381 | 0.00746179 | intron-variant | USP10 | GRCh38.p7 | 16:84760125 | CTTTTTTCATCATTT[A/G]TGAGTTCATTGTAGT | 9100 |
| rs764524035 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84743748 | TCAGAGGTGTAAACT[A/G]TAAAAATACGTCTGT | 9100 |
| rs764572718 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84754630 | TTTTTAACCTGCCTG[C/T]GCCTCAAAATAAGCA | 9100 |
| rs764602530 | in-del | -/AT | | | intron-variant | USP10 | GRCh38.p7 | 16:84751585 | TTCCACTTCAGAAAC[-/AT]AAGTTGATCTGTAGT | 9100 |
| rs764603684 | snp | A/G | 5.10478e-05 | 0.00505186 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84760198 | AAAATCGTGAGGGAT[A/G]TTCGCCCTGGAGCTG | 9100 |
| rs764611649 | in-del | -/TTTTTTTT | | | intron-variant | USP10 | GRCh38.p7 | 16:84711722 | AGGAAGGGCTAGCTT[-/TTTTTTTT]TTTTTTTTTTTTGTC | 9100 |
| rs764696957 | snp | A/G | 1.65861e-05 | 0.00287972 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84778992 | CATCGATGACCAGAC[A/G]GTCAAGGTGATCAAC | 9100 |
| rs764703817 | in-del | -/A | | | intron-variant | USP10 | GRCh38.p7 | 16:84754991 | AGACTTTGTCCCAGA[-/A]AAAAAAAAAAAGGAG | 9100 |
| rs764706382 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84709460 | GTTACTGTCTTTATT[C/T]TGAGAAAAGTGTGGA | 9100 |
| rs764709457 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84748261 | GCATGGTGGGGTCCT[G/T]TTAAAAATGTGCATT | 9100 |
| rs764712068 | snp | A/G | 2.99361e-05 | 0.00386874 | intron-variant | USP10 | GRCh38.p7 | 16:84768381 | CACACTTGATTTTGA[A/G]CCTTTCTACTAAGGT | 9100 |
| rs764716580 | in-del | -/GGGG | | | intron-variant | USP10 | GRCh38.p7 | 16:84757394 | AAGGAGGGAATGAGA[-/GGGG]TGGGGGTGTGTGTGT | 9100 |
| rs764736149 | snp | A/G | 1.65858e-05 | 0.00287969 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744776 | TGTACAGCTTCCAAA[A/G]TAACCCCTGATGGTA | 9100 |
| rs764740333 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84765349 | GAGTAGCTCTTGTCC[C/G]ATGTTCCACATCAGA | 9100 |
| rs764763372 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84775265 | TTCTTCATTAAAACA[C/G]TGATGAAGGGGTTTA | 9100 |
| rs764774503 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84703958 | TCCAGTGTTCTGTTA[C/T]GTGGAACTGATAGGA | 9100 |
| rs764782110 | snp | A/C | 1.65833e-05 | 0.00287948 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744703 | CACTTTGCCGAGAAC[A/C]CCCAGCTACAGTATT | 9100 |
| rs764802279 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84736121 | GGGCGTGTCACTTCT[A/G]CAGCACAGTTTGGCC | 9100 |
| rs764818903 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84777601 | TGCTGTTCAGTCTCC[G/T]CCGGGGTCCCTGCAC | 9100 |
| rs764821480 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84731675 | ATTGCCTTCCATAGC[C/T]TTGTTGATTTTGCTA | 9100 |
| rs764829848 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84704443 | CCATTGGATTACTGT[C/G]ATTTGTCACTTTAGT | 9100 |
| rs764862429 | snp | A/G | 1.65704e-05 | 0.00287836 | intron-variant | USP10 | GRCh38.p7 | 16:84758821 | CTGTATCCTTCCTGG[A/G]CGCCGTCCGCAAGGC | 9100 |
| rs764874519 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84724342 | TAGCTCGGAATCTCC[A/G]TGAAAGCACTTAATA | 9100 |
| rs764909546 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84776985 | ATCCAGCTAATTTTT[C/G]TATTTTGAATAGAGA | 9100 |
| rs764940074 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745462 | TCCTGCTGACGGCAC[A/G]GGCTCTGCATCAGGC | 9100 |
| rs764974007 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84749444 | GGGAAAGAGGGAGTA[A/G]GGAATGATTTAGACA | 9100 |
| rs765022343 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84773086 | CAGTGAGAGTCCCTT[C/G]TAACCTCTAGTTGTG | 9100 |
| rs765028751 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84749900 | ACATTTTGTTCCATT[A/G]GCTGTTTTTCAAGTG | 9100 |
| rs765050570 | snp | A/G | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698879 | GGATTCCGGGTGTGA[A/G]CCGCTGCGCCTGGCC | 9100 |
| rs765056331 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84773801 | GGCTAAGTCAAAGAA[A/G]GCATCCTCGGCCTCT | 9100 |
| rs765078012 | snp | G/T | 3.4659e-05 | 0.00416273 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745196 | AGTGACACCAGGACT[G/T]CAGGGCAGCCAGAGG | 9100 |
| rs765095324 | snp | A/G | 0.000151903 | 0.00871368 | intron-variant | USP10 | GRCh38.p7 | 16:84759340 | GTTCATTTCCTTTAC[A/G]CTTCCTTACTGCCAC | 9100 |
| rs765100189 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84735130 | CCCCCGCCCCGCCTC[A/G]GGGGGGTTCTCATGC | 9100 |
| rs765111774 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84764480 | CTGCAGGGGACAGGG[A/G]GCTCCTCCCTTCTAC | 9100 |
| rs765117133 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779338 | AAACCCATATTTCTG[-/A]AATAATGCTGATTCC | 9100 |
| rs765133251 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84731283 | GCTCCCGGCCTCTAC[-/T]TTTTTTTTTTTTTTT | 9100 |
| rs765165839 | snp | A/G | 4.96718e-05 | 0.00498331 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745259 | TTCCCTGCAGAGGCT[A/G]GCAGAGACACCCTGT | 9100 |
| rs765170240 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84724620 | GAGGGAACAAAACTT[C/T]TCTTCCTCCTTCTTC | 9100 |
| rs765195379 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84754404 | TTTAACGACGTCGTA[C/G]CAGAATGGCCTTTCA | 9100 |
| rs765212311 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84707988 | GAGGTTGAGGTGGGA[C/G]GATCGCTTGAACCTG | 9100 |
| rs765232247 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84747894 | TGAATACAGCTTTCA[G/T]AATGTATTTATTGCA | 9100 |
| rs765264387 | snp | A/G | 1.66413e-05 | 0.0028845 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84762993 | GACCTTTTCAGGGTC[A/G]ACAAGAAGATGCTGA | 9100 |
| rs765264442 | snp | A/G | 3.70631e-05 | 0.00430467 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745586 | TATTCCCCTCCCGCC[A/G]TATCTCCCCTGGTTT | 9100 |
| rs765276523 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84728884 | GCTCACTGCAGCCTC[C/T]GCCTTCCAGGTTCAC | 9100 |
| rs765289530 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84701676 | AATTCAAGGTTGATT[A/G]AAATGTTAATTAATG | 9100 |
| rs765296014 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84775090 | GGGAGAATGTTGTTA[G/T]CCATTTTCTGCTGCT | 9100 |
| rs765354386 | snp | C/G | 2.33119e-05 | 0.003414 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745648 | TGTTCCGGTTTCAGA[C/G]GATCCTGTAGCCATA | 9100 |
| rs765393693 | snp | C/T | 1.65844e-05 | 0.00287957 | intron-variant | USP10 | GRCh38.p7 | 16:84775147 | TTCAAGCCATTGATA[C/T]TTTGTTTTCCAGAAC | 9100 |
| rs765460807 | snp | C/T | 5.06086e-05 | 0.00503008 | intron-variant | USP10 | GRCh38.p7 | 16:84760314 | TAGTATCAAGTGTTG[C/T]CTTTTGTTCCAGTGT | 9100 |
| rs765474457 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84742487 | TTTCCCTCCCTCGCC[C/G]CCTGCCTTGTAGTCC | 9100 |
| rs765477231 | snp | C/G | 1.69049e-05 | 0.00290726 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779090 | TGCTGTAAACCCTGT[C/G]TGCGCTGTGTGTGCG | 9100 |
| rs765502891 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84724944 | CAGCTAGCACCCATA[A/G]CTTACTGGGCTTTGA | 9100 |
| rs765516516 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84770936 | CTGGGCATGGTGGTG[C/T]GCACATGTAGTCCCA | 9100 |
| rs765531750 | in-del | -/AG | | | intron-variant | USP10 | GRCh38.p7 | 16:84726175 | TTTATTCAAATTTCC[-/AG]AGAGATGAAACTTTC | 9100 |
| rs765536821 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84766254 | CAGTTGAGCAGCCAT[G/T]TGACCTTGAACAAGT | 9100 |
| rs765541554 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84767208 | ACACCCATTTTATTC[C/T]GTTGAGAAACTAGGT | 9100 |
| rs765566148 | snp | C/G | 6.68181e-05 | 0.00577967 | intron-variant | USP10 | GRCh38.p7 | 16:84700128 | TAGCCGCCGGTCTGC[C/G]CCTTCGGCCGGAAGG | 9100 |
| rs765568254 | snp | C/T | 3.31395e-05 | 0.00407046 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84759922 | GAGTTCACTAATATG[C/T]CAGTACCTCCAAAAC | 9100 |
| rs765646412 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84743189 | GGAAACAAAAAATAA[A/G]TAGTAGCCAAAGGAA | 9100 |
| rs765650966 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84731222 | CTGACCTCATGATCC[A/G]CCCACCTCGGCCTCC | 9100 |
| rs765655689 | snp | C/G | 3.45644e-05 | 0.00415704 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84768247 | TTTGCAGCCATTTTT[C/G]ACGTTGCAGTTGGAT | 9100 |
| rs765686423 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84717001 | CTTCGGGATTACATG[A/G]GATAGAGCATAGCAG | 9100 |
| rs765696772 | in-del | -/TT | 0.0373249 | 0.131413 | intron-variant | USP10 | GRCh38.p7 | 16:84732445 | GACTTCTTCTTCTTC[-/TT]TTTTTTTTTTTTCTT | 9100 |
| rs765716740 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84761817 | TCCCAGACACCAGCC[A/T]AGGGGCAACCTTGCA | 9100 |
| rs765741499 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717295 | TTTCTCGGGAGGTCT[C/G]CTGCCACCCAAAAAA | 9100 |
| rs765758460 | snp | C/T | 8.35387e-05 | 0.00646238 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744926 | CTTGGACAAAGGGAG[C/T]GTAAAAAGAAGAAAA | 9100 |
| rs765779272 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84700786 | ACTAACGCACCCTGC[C/T]TGAACAGTAGCTAAA | 9100 |
| rs765787014 | snp | A/G | 1.67539e-05 | 0.00289425 | intron-variant | USP10 | GRCh38.p7 | 16:84764278 | GGTTTGTGCTTTTCT[A/G]GAATAACTTAATATT | 9100 |
| rs765809564 | snp | C/G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84753739 | CATTTCTAACAAATA[C/G/T]GAGTGGAGTCATTTG | 9100 |
| rs765812676 | snp | A/G | 2.68165e-05 | 0.00366163 | intron-variant | USP10 | GRCh38.p7 | 16:84744615 | GGGTTCTTAACTAAT[A/G]GTTTTCTTTCTAAAC | 9100 |
| rs765836087 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84736697 | CTGAGTCAATAAGCC[C/T]CCGATGACATAGTGT | 9100 |
| rs765862245 | snp | A/G | 1.93287e-05 | 0.00310869 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84778896 | GGGCTCTCTTCCAGT[A/G]GTCTACCATCACGGC | 9100 |
| rs765881080 | snp | C/T | 1.65864e-05 | 0.00287974 | intron-variant | USP10 | GRCh38.p7 | 16:84775269 | TCATTAAAACACTGA[C/T]GAAGGGGTTTACAGC | 9100 |
| rs765906474 | in-del | -/TA | | | intron-variant | USP10 | GRCh38.p7 | 16:84763411 | TATACACACACTGTG[-/TA]TATATATATATGTCT | 9100 |
| rs765913667 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84712128 | TTCATCAGTTGATCT[C/G]TTTTCTGTGAGAAGG | 9100 |
| rs765919290 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84763602 | AATACCGACTTTGCA[C/G]AGCATCTTCAAATTT | 9100 |
| rs765919564 | snp | A/G | 1.65913e-05 | 0.00288017 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744697 | CAGTGACACTTTGCC[A/G]AGAACCCCCAGCTAC | 9100 |
| rs765924859 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84738085 | TGAGCAGGGTTCTAA[C/G]AGCTCTCTGCCTTGT | 9100 |
| rs766005266 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84733370 | TTAAAATATGTAGCA[-/T]TTTTTTCTGAAAGTA | 9100 |
| rs766039418 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84755588 | CTGCAGTGAGGCATA[A/G]TCACGCCACTGCACT | 9100 |
| rs766044773 | snp | C/T | 2.85327e-05 | 0.00377697 | intron-variant | USP10 | GRCh38.p7 | 16:84764040 | CTTTTTTTTTTTTGC[C/T]GTTCTTGTCGTAAAT | 9100 |
| rs766045515 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84745787 | CTGTGTGTTAATAGC[A/G]ACGTCTGAAGGATGC | 9100 |
| rs766046526 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84775866 | CCTTCCCTTTTATCC[C/T]TCTTTCTCTTTTATA | 9100 |
| rs766087460 | in-del | -/TC | 0.00612624 | 0.0550053 | intron-variant | USP10 | GRCh38.p7 | 16:84732458 | TCTTTTTTTTTTTTT[-/TC]TTTTTGAGATGGAGT | 9100 |
| rs766112367 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84764413 | TCTCTTGCACTTCCT[C/G]ATGCTTCCCTTGTCA | 9100 |
| rs766154042 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84759583 | AATGAGTCCTATAAT[A/T]CTGTCTTTTTTTAAA | 9100 |
| rs766169917 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84751586 | TCCACTTCAGAAACA[G/T]AAGTTGATCTGTAGT | 9100 |
| rs766180809 | in-del | -/T | 3.20046e-05 | 0.00400016 | splice-donor-variant | USP10 | GRCh38.p7 | 16:84760276 | GCCTGTCTGAAAAGG[-/T]TTTGAGACTTCTCTG | 9100 |
| rs766192651 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779624 | AAAAATTTTAATAAT[C/T]GTACTGAGAGAAACT | 9100 |
| rs766218064 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84726056 | TCGGAAACTGCAGGT[A/G]CAAATGCAGCAGCAA | 9100 |
| rs766225572 | snp | C/T | 4.96882e-05 | 0.00498414 | synonymous-codon, nc-transcript-variant, intron-variant | USP10 | GRCh38.p7 | 16:84758801 | GAACTGGTGCTACAT[C/T]AATGCTGTATCCTTC | 9100 |
| rs766229331 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84721166 | CAAAGTGCTGGGATT[A/G]CAGGTGTGAGCCACC | 9100 |
| rs766244015 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84733427 | GTGACTCTCTTATTT[C/T]TTTTCAGTATATTTT | 9100 |
| rs766250718 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84778756 | AGCATTGGTTTGTGT[C/G]ATGACATCTCTCTGT | 9100 |
| rs766299005 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84734221 | TAGGATTTTAACAGT[C/G]TTCATTCCCATCAGC | 9100 |
| rs766313772 | snp | C/T | 3.40356e-05 | 0.00412512 | intron-variant | USP10 | GRCh38.p7 | 16:84759328 | TGTGGTGTGTCTGTT[C/T]ATTTCCTTTACGCTT | 9100 |
| rs766327084 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84761718 | AGCAAAGTGTTCAGC[A/G]GAAAGCACATTGCTT | 9100 |
| rs766329393 | snp | C/T | 2.37883e-05 | 0.00344871 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84760224 | AGCTGCCTTTGAGCC[C/T]ACATATATTTACAGA | 9100 |
| rs766349122 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84752164 | TTTTGTGTCTTTTAT[C/G]AGTCATTCTGGCATT | 9100 |
| rs766363764 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84743860 | CAATTCTAACTTTTT[A/C]TTTTGGTATTTTTGG | 9100 |
| rs766406311 | snp | C/G | 1.65696e-05 | 0.00287828 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84772669 | TGAATATCCTGTGGA[C/G]TTGGAAATTAGTAAA | 9100 |
| rs766417243 | snp | A/T | 1.71021e-05 | 0.00292416 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745482 | CTGCATCAGGCACCC[A/T]TCCTGTCAGCCAGCC | 9100 |
| rs766423241 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84710008 | GGGTGCGAGGCTCAC[G/T]CCTGTAATCCCAGCA | 9100 |
| rs766426791 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84736114 | GAGGGGAGGGCGTGT[C/T]ACTTCTACAGCACAG | 9100 |
| rs766472004 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84700564 | GAGATTTGGGGGTGC[C/T]CTGTTGCCCCTTTGC | 9100 |
| rs766479680 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84709085 | TTACCGAGTGGCTGC[C/T]GTGTACCAGGCACTG | 9100 |
| rs766493296 | snp | C/T | 8.63401e-05 | 0.00656983 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745177 | TTTCCCCGGAGCACT[C/T]GGCAGTGACACCAGG | 9100 |
| rs766521505 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84728827 | TTTTTGAGACGGAGT[C/T]TTCCTCTGTCATTCA | 9100 |
| rs766525080 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84752800 | CAGTTGATGGTTATC[A/G]AAATGAGTCAGGATG | 9100 |
| rs766532692 | snp | C/T | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699018 | GCAAGAGCAGACTCT[C/T]TGTAGGTGTTTGTTG | 9100 |
| rs766542649 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84750905 | TCAAAACCTGTTTAT[A/G]TGATTTTTCACAGTG | 9100 |
| rs766554088 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84755384 | CTTGCACCCATGATC[C/G]TGTCTCCTTCCTCAG | 9100 |
| rs766573901 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84745927 | TCTGTTGACAAGTTA[C/G]ATTTCCATTTCTTGC | 9100 |
| rs766609251 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84765798 | TGACTGGGCTGGAGT[A/C]CCTGGGCACCTGGCT | 9100 |
| rs766630377 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84731639 | AATCCTTTTTTCTCG[A/C]AACTTTCAAAATGTT | 9100 |
| rs766658586 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84774353 | GACGGACTCTTGTGT[C/T]GGTGTAAGTGGTACT | 9100 |
| rs766704494 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84761938 | CGTGCAGAGCATGCA[C/G]TCACGTGAACAGCTG | 9100 |
| rs766708121 | snp | A/G | 3.33461e-05 | 0.00408313 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764255 | CGGCATTTTTGGTGG[A/G]CACATCAGGTTTGTG | 9100 |
| rs766748191 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84741732 | ACAGTTAGTGACAGG[C/T]CTGCTTTTCTCTGCA | 9100 |
| rs766768436 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84746929 | CTTTTTATTCTTACT[A/T]TCCTATAAGCTTTTT | 9100 |
| rs766786604 | snp | C/T | 1.66316e-05 | 0.00288367 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744852 | GCTCTGCCCTCGCTT[C/T]GGATGGAAGTTCTAA | 9100 |
| rs766860274 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84763701 | TTGCGATTGGTTGCC[A/G]TGGATCAAGTGGCAT | 9100 |
| rs766865727 | in-del | -/TTTTC | | | intron-variant | USP10 | GRCh38.p7 | 16:84748303 | GTCATGAGAATTTTA[-/TTTTC]TTTTCTTTATTTTTG | 9100 |
| rs766875820 | snp | A/G | 3.34146e-05 | 0.00408732 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744919 | AGGTGGTCTTGGACA[A/G]AGGGAGCGTAAAAAG | 9100 |
| rs766891233 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84701566 | ACAAGTAAAAGGCTC[A/C]TTATGAATTAATGTG | 9100 |
| rs766897212 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84743307 | AGGATTGTGCTGCCA[C/T]CACCCTTCACCCCCC | 9100 |
| rs766900844 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84769382 | GTAGAAGTTATGCCT[A/G]ATCTTCTACCGTATT | 9100 |
| rs766929063 | snp | A/T | 1.6574e-05 | 0.00287867 | missense, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779009 | TCAAGGTGATCAACC[A/T]GTACCAGGTGGTGAA | 9100 |
| rs766958060 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84761121 | ATGGGAACATGGTGT[C/T]AGGGATGCAGAAATG | 9100 |
| rs766961044 | snp | A/G | 1.65707e-05 | 0.00287838 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84759900 | GTTTAGTGTTCGGCT[A/G]ATGAATGAGTTCACT | 9100 |
| rs766963228 | snp | A/G | 1.72121e-05 | 0.00293356 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745279 | AGACACCCTGTCAAG[A/G]ACAGCTGGGGCTCAG | 9100 |
| rs766967520 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84746787 | TCAATAAGAAATTAA[C/G]CTTAACCTACTGTAA | 9100 |
| rs767001847 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84725917 | GAGGGAGAATACTTT[A/G]TACTTCTCAGCTTCT | 9100 |
| rs767056178 | in-del | -/A | 2.40729e-05 | 0.00346927 | intron-variant | USP10 | GRCh38.p7 | 16:84764064 | CGTAAATAGTAGTGT[-/A]AGCAGATGCTCTCCT | 9100 |
| rs767068309 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84743823 | AGTATTGAAGGCTTC[A/C]CAAGAGATATTTAAA | 9100 |
| rs767076420 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779322 | TTTAGAAAATACACA[A/G]AAACCCATATTTCTG | 9100 |
| rs767099986 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718948 | CAGGCGCCCGCCACC[A/G]CACCCAGCTAATTTT | 9100 |
| rs767161297 | snp | G/T | 1.68139e-05 | 0.00289943 | intron-variant | USP10 | GRCh38.p7 | 16:84759509 | GTGTTAAGTGGTGGG[G/T]TTTTTCCCGTCTGAT | 9100 |
| rs767190510 | in-del | -/A/GAGAG | | | intron-variant | USP10 | GRCh38.p7 | 16:84764933 | ACGAGAGAGAGAGAA[-/A/GAGAG]AAAAAAATATATATA | 9100 |
| rs767199236 | snp | C/G | 4.98368e-05 | 0.00499158 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84768209 | TCTGTGGTTTACCAG[C/G]AGAGTTCAAAAGAAT | 9100 |
| rs767201038 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84702214 | GGCGCCCACCACCAT[A/G]CCTGGCTAATTTTTT | 9100 |
| rs767206798 | snp | A/C | 1.65707e-05 | 0.00287838 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84775181 | TTTCTCCAGGGGTTA[A/C]AAATAAGAATTTTAA | 9100 |
| rs767212858 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84704542 | ATTGAAGTGTTCTCC[C/G]AAAAGGTCTTTCTTT | 9100 |
| rs767232572 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84766381 | CCTGGGAAACACCCA[A/G]CCCTGACCACTGTCT | 9100 |
| rs767240707 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84740143 | TTTCGTTAAATGAAG[A/G]TGATTTAGATTGCAC | 9100 |
| rs767249866 | snp | C/T | 0.000166099 | 0.00911164 | utr-variant-5-prime, missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84700106 | ATGGCCCTCCACAGC[C/T]CGCAGGTAGCCGCCG | 9100 |
| rs767257203 | in-del | -/TAATCCTAGCTAC | | | intron-variant | USP10 | GRCh38.p7 | 16:84774128 | GGTGGTGGGTGCCTG[-/TAATCCTAGCTAC]TTGGGAGGCTGAGGC | 9100 |
| rs767287190 | snp | A/C/G | 0.000116215 | 0.00762203 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744690 | TTGAACCCAGTGACA[A/C/G]TTTGCCGAGAACCCC | 9100 |
| rs767293546 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84733368 | TTGTTAAAATATGTA[A/G]CATTTTTTCTGAAAG | 9100 |
| rs767331804 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84721784 | CTCACTGCAACCTCC[A/G]CCTCCCGGGTTCAAG | 9100 |
| rs767349829 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84737243 | TTCACAAGGCCGCAG[C/G]ACTGTTTTCACACTG | 9100 |
| rs767354962 | snp | C/G | 3.06941e-05 | 0.00391741 | intron-variant | USP10 | GRCh38.p7 | 16:84744601 | GAGTTTGTAGAACTG[C/G]GTTCTTAACTAATAG | 9100 |
| rs767405840 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84750837 | AGCTCTTGAACAGCT[C/G]TGAAAACATTGCGTT | 9100 |
| rs767429003 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84758869 | CCCTCCTTTGGGTGC[A/C]TGTGACTTAGCTCAG | 9100 |
| rs767436735 | snp | A/G | 6.77989e-05 | 0.00582193 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745127 | AGCCCCCAGAACTCC[A/G]CAGACTCTGTCAGTG | 9100 |
| rs767541130 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84716914 | ATGATAAATGGTTAC[A/G]CAACTTAAAATAGAA | 9100 |
| rs767542093 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84777889 | GCTGCCCTGTCATTC[C/G]CCGCGGAATGCTGCC | 9100 |
| rs767553813 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84741659 | TCTTTACTCTGTTCC[A/C]TCTAAGTCCTGCCTT | 9100 |
| rs767570809 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84707013 | TTAGCTTGTTTGAGC[A/C]TTTACAGCAACTCTG | 9100 |
| rs767571484 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84727610 | TTAAATCCATTTGCT[G/T]AATCATTTGTGTGTG | 9100 |
| rs767572484 | snp | A/T | 1.65778e-05 | 0.002879 | intron-variant | USP10 | GRCh38.p7 | 16:84775264 | CTTCTTCATTAAAAC[A/T]CTGATGAAGGGGTTT | 9100 |
| rs767605848 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84734560 | AGGGCTTTAAGCTTC[A/C]CATGTTAGGTGAACC | 9100 |
| rs767608723 | snp | C/G | 3.33356e-05 | 0.00408248 | intron-variant | USP10 | GRCh38.p7 | 16:84733420 | GTGATCAGTGACTCT[C/G]TTATTTTTTTTCAGT | 9100 |
| rs767610400 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84772857 | ACTAAAATTCTCATG[A/C]AAATGGCCTGTTGAA | 9100 |
| rs767628382 | snp | C/T | | | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84716469 | TTGTGCTTCAGTGGA[C/T]GAAATACAGACTGAC | 9100 |
| rs767682466 | snp | A/G | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84697984 | CTTCCAAAGTGCTGA[A/G]ATTACAGGTGTGAGC | 9100 |
| rs767684504 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84708902 | CGTTAGGAGTATAGA[C/G]CTGAAGAGAGAATTC | 9100 |
| rs767691522 | snp | G/T | 0.000215291 | 0.010373 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84772543 | CTTTGTGTCTTAGGT[G/T]GAGATAAGTCGAAGA | 9100 |
| rs767712225 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84735972 | TGGTTGGGCCTGTGG[A/G]TGTGTGAGTGGCGAG | 9100 |
| rs767733285 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84755441 | CTTGCTGTCTTCACT[C/G]CTACACGCTGCCCCC | 9100 |
| rs767737439 | snp | A/G | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698955 | CCTATTTTATGTAAC[A/G]TGGGAATGGATCTTC | 9100 |
| rs767773699 | snp | C/T | 6.661e-05 | 0.00577067 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84745038 | CCAATTCAGCAGTCC[C/T]GAACAGTGTCAGTGC | 9100 |
| rs767795753 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84727158 | AACGATGAACTTACT[C/T]GTGCTTTTTAGTCTC | 9100 |
| rs767802380 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84722650 | CACTGAAACCTTCAC[C/T]TCCCAGGTTTAAGCA | 9100 |
| rs767825816 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84735473 | CCACTTCCACAGGCT[C/T]GGAGGGTTTGGGCAC | 9100 |
| rs767840729 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84761025 | TGCAGGATACCACCA[C/G]GGGTAGCATAGGGTC | 9100 |
| rs767848739 | snp | C/T | 3.49956e-05 | 0.00418289 | missense, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84778922 | ACGGCAACAGTGCGA[C/T]GGGCGGCCATTACAC | 9100 |
| rs767873085 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84748731 | TTTTAGAACATTCTA[C/G]TTAGTCATATGACTT | 9100 |
| rs767892970 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84742681 | TCGTCTGCCTGGCAC[A/G]TTGGGCTCTGAGCTC | 9100 |
| rs767907202 | snp | A/C | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699460 | ACGTTTTGTTTTTGT[A/C]TGTTTTGCTTTTTTC | 9100 |
| rs767938676 | snp | A/C/T | 8.2887e-05 | 0.00643719 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779004 | GACAGTCAAGGTGAT[A/C/T]AACCAGTACCAGGTG | 9100 |
| rs767943187 | snp | C/T | 3.41693e-05 | 0.00413322 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745479 | GCTCTGCATCAGGCA[C/T]CCTTCCTGTCAGCCA | 9100 |
| rs767962691 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84777146 | GGGAGAAGCAATCTC[A/G]CGCACAAGCTTTTCA | 9100 |
| rs767967072 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84754842 | GGGCCCCTAACTCAG[-/T]TAAGAACATGAAAGG | 9100 |
| rs767973597 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84729903 | TATGGTGTATTTTTT[A/T]GCGTGACATGTTTTC | 9100 |
| rs767983509 | snp | C/G | 3.31906e-05 | 0.0040736 | missense, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84733490 | TCTTTGTGACTCCTC[C/G]ATCTTCAGTTGAGGT | 9100 |
| rs768007397 | snp | A/C | 1.72101e-05 | 0.00293338 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779108 | CGCTGTGTGTGCGCC[A/C]AGTGCCCGCTTCGTA | 9100 |
| rs768024164 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717802 | GAGGTCCTAGTCTCT[A/G]GTCCTCAGGTGTATG | 9100 |
| rs768026965 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84730755 | AAAACTTTAGGCTGT[A/G]TATGAACTGAAATAA | 9100 |
| rs768032124 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84748461 | GGTGCCTGGCACCAC[A/G]CCAGGCTAATTTTTG | 9100 |
| rs768033312 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84703774 | TGTGAGCCAGTGGTC[A/G]CCTTAGTGGTTTGTA | 9100 |
| rs768039687 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84775825 | GTATCATTTTTTCTG[C/G]CACATCATCTTCCCT | 9100 |
| rs768043331 | snp | C/G | 3.31763e-05 | 0.00407272 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744782 | GCTTCCAAAATAACC[C/G]CTGATGGTATCACTA | 9100 |
| rs768062869 | snp | A/T | | | missense, nc-transcript-variant, intron-variant | USP10 | GRCh38.p7 | 16:84759405 | CCGATGTACCACCTG[A/T]TGAAGTTCATTCCTC | 9100 |
| rs768071499 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84749226 | TAAAACATACTCAGT[A/T]TGTTACAAGTCAGAT | 9100 |
| rs768071505 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84741216 | TTTTATCTCCAGTAA[C/T]ATCAGGGAGTGATTA | 9100 |
| rs768081329 | in-del | -/AGTC | | | intron-variant | USP10 | GRCh38.p7 | 16:84705927 | GGGTTTCACCATGTT[-/AGTC]AGGCTGGTGTGGAAC | 9100 |
| rs768085304 | snp | C/T | 0.000156213 | 0.00883642 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84700096 | ACGGGCAGCCATGGC[C/T]CTCCACAGCCCGCAG | 9100 |
| rs768087109 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84740840 | GAACTCAGGTCAACT[C/T]TTCACCTCCTGGTCT | 9100 |
| rs768094887 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84768535 | TTGAAACGTGATCCC[A/G]AGGGCCTCTTTTAGC | 9100 |
| rs768112352 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84766929 | ATGTTTTTCAGTTTC[C/T]CCAGGAAGACTTCCC | 9100 |
| rs768162158 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84774716 | ACCTCGTGATCGCCC[A/G]TCTCAGCCTCCCAAA | 9100 |
| rs768200274 | snp | C/G | 9.38306e-05 | 0.00684883 | intron-variant | USP10 | GRCh38.p7 | 16:84768150 | AAGGGAAAGTGGCAA[C/G]GAGTGGTCTCTTAAT | 9100 |
| rs768214395 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84713422 | TCACCCTGTCTGCTT[G/T]CTCCCTCTCCAGAGC | 9100 |
| rs768225319 | snp | G/T | 1.66974e-05 | 0.00288936 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744907 | TGATGGTGTCTCAGG[G/T]GGTCTTGGACAAAGG | 9100 |
| rs768240816 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84733925 | TTGTCGTTTATTTTA[A/C]GCTAACGTTGTATTC | 9100 |
| rs768250953 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84751230 | CCAGGTGTGTAGTTG[C/G]CTATACCATCTAGGC | 9100 |
| rs768315373 | snp | A/G | 8.31566e-05 | 0.00644759 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744981 | ATTTGAAAGATGGTG[A/G]CGATGATAGTATCTC | 9100 |
| rs768324336 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84736433 | TGGCAAGATAAGGTG[A/G]CTAGTAATTTAGTGG | 9100 |
| rs768331697 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84715150 | GGCCGGTCTGGTCTC[A/G]ACCTCCTGACCTCAA | 9100 |
| rs768359806 | in-del | -/GTTTTAGGAAGTTTGGCGAGTGGGTGAGGGCCCAGGGATGGGG | | | intron-variant | USP10 | GRCh38.p7 | 16:84776246 | CAGCTCACGCCCGAT[lengthTooLong]GCCCAGGGGTGAGGG | 9100 |
| rs768359817 | in-del | -/GGGGGTGTGTGT | | | intron-variant | USP10 | GRCh38.p7 | 16:84757399 | GGGAATGAGAGGGGT[-/GGGGGTGTGTGT]GTGTGTGTGTGTGTG | 9100 |
| rs768370980 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84707881 | CTCAGGAGTTTGGGA[C/T]CAGCCTGGGCAACGT | 9100 |
| rs768377298 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84728725 | TCCCTTTTTGTAGTT[C/T]TATCAGCATATGCAA | 9100 |
| rs768381866 | snp | C/T | 1.65693e-05 | 0.00287826 | intron-variant | USP10 | GRCh38.p7 | 16:84759965 | AGTAAAAATGAGTTT[C/T]GTTGATGCTATTACA | 9100 |
| rs768397962 | snp | C/T | 1.65729e-05 | 0.00287857 | intron-variant | USP10 | GRCh38.p7 | 16:84775252 | TGTACGACATTACTT[C/T]TTCATTAAAACACTG | 9100 |
| rs768423361 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84740238 | TTAATGAATTGTTGC[C/G]TTAATTAAATGGTAA | 9100 |
| rs768437599 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84738733 | GCCCTGTGTTTTCCT[A/G]TTTGTCATAATTCTC | 9100 |
| rs768447974 | snp | C/T | 3.41723e-05 | 0.0041334 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779102 | TGTGTGCGCTGTGTG[C/T]GCGCCCAGTGCCCGC | 9100 |
| rs768500491 | snp | C/T | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699838 | CCGGCCGCTTCCGCC[C/T]GAGGGTCGCGGGGCT | 9100 |
| rs768521220 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84753369 | AGTTGTTGGTTTTCT[C/T]AGACTCTCACATAAA | 9100 |
| rs768522872 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84762443 | TGCCTGTAATCCCAG[C/T]ACTTTGGGAAGCCAA | 9100 |
| rs768538407 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84737034 | ACCTCGTGGTCTGCC[C/T]GCCTCGGCTTCCCAA | 9100 |
| rs768554091 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84701423 | TTTTTACAAATGTAT[A/T]GCCCAAAGATTTTAA | 9100 |
| rs768572637 | snp | C/T | 2.47822e-05 | 0.00352001 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84768337 | ATCTGTCCAAGGTTA[C/T]ACCACAAAAACCAAA | 9100 |
| rs768574171 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84754239 | TAGGATCATTATAAG[A/G]GATTAATAACAGAAT | 9100 |
| rs768574872 | snp | C/T | 3.31483e-05 | 0.004071 | intron-variant | USP10 | GRCh38.p7 | 16:84759887 | ATTTTTTCCCCATGT[C/T]TAGTGTTCGGCTAAT | 9100 |
| rs768589747 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84729516 | AGATACATGTAGTTT[A/T]TCTGCCATGAGCATA | 9100 |
| rs768603540 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84728775 | CAATAAAGTTGTCAT[A/G]TTCTGTTTTATAAGC | 9100 |
| rs768632158 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84775032 | GCAACTGAAGGGATA[G/T]AGTGTTGTTTTGTTC | 9100 |
| rs768655406 | snp | A/G | 0.000265935 | 0.0115281 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764138 | CAATGAAGAAGAGCA[A/G]GAAGAACAAGGTGAA | 9100 |
| rs768664325 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84721600 | TGGTGTGATCATAGC[A/T]CACTGCAGCCTTGAC | 9100 |
| rs768696341 | in-del | -/G | 3.30191e-05 | 0.00406306 | intron-variant | USP10 | GRCh38.p7 | 16:84768393 | GAACCTTTCTACTAA[-/G]GGTGCTCTGGTTTGG | 9100 |
| rs768726187 | in-del | -/TTT | | | intron-variant | USP10 | GRCh38.p7 | 16:84730977 | TATAGCATTTCTACC[-/TTT]TTTTTTTTTTTTTTT | 9100 |
| rs768730949 | snp | A/C | 1.66341e-05 | 0.00288388 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744678 | TCGATGAAGTCATTG[A/C]ACCCAGTGACACTTT | 9100 |
| rs768734797 | snp | C/G | 4.14233e-05 | 0.00455082 | intron-variant | USP10 | GRCh38.p7 | 16:84764075 | GTGTAAGCAGATGCT[C/G]TCCTTTTCAGAACTT | 9100 |
| rs768771475 | in-del | -/CTT | 3.31793e-05 | 0.00407291 | intron-variant | USP10 | GRCh38.p7 | 16:84758699 | AATTTCTGAAATATG[-/CTT]CTTCACTCTTTCAGA | 9100 |
| rs768812671 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84777190 | GCTCCTGTCAGGGGG[C/G]CTTGCAGGTGTGAGT | 9100 |
| rs768898125 | snp | C/T | 0.000301245 | 0.0122691 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745432 | GGACCCAACCAAACC[C/T]GAGAGTGCATCACCT | 9100 |
| rs768921452 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84703707 | GAGTAGATGTTTTAA[A/G]TTTGTGAGCCAGTGG | 9100 |
| rs768934435 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84749764 | CTAAAAGAATCACGT[A/G]TAAGGGATTTTGAAG | 9100 |
| rs768940787 | snp | A/C | 1.72077e-05 | 0.00293318 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745167 | CTGACAGTCCTTTCC[A/C]CGGAGCACTCGGCAG | 9100 |
| rs768972633 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84704268 | TGGTTGCTGAGGACA[C/G]TTATTACTGGTACTA | 9100 |
| rs768999219 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84776754 | CCGACTCTGCAACCT[A/G]CCTCGCCCCGGGACC | 9100 |
| rs769002308 | snp | C/T | 3.31208e-05 | 0.00406931 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84772588 | ACTCCCTCCTGTCCT[C/T]GTGCTGCACCTGAAA | 9100 |
| rs769005838 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84726405 | CAAGGTCTTTGTTTT[C/T]CCTTTAGCAGGAACA | 9100 |
| rs769009684 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84778125 | TGTGTGTGTTTTGTT[A/C]TGTTAAAACATAGAA | 9100 |
| rs769031793 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84773430 | CTCCGTCCCCTGGCA[C/T]AGCAACCCCACCTCA | 9100 |
| rs769035063 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84751825 | CTGTACCTTGCATTT[C/T]CAGGGATTTTCAATG | 9100 |
| rs769059082 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84727111 | AGCCACCAATATGTC[C/G]TAAGCTCTGCACTTT | 9100 |
| rs769079031 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779867 | GTACACAGTTTAGTG[A/G]TATCTAGGAGTATAA | 9100 |
| rs769107453 | snp | C/T | 1.65721e-05 | 0.0028785 | intron-variant | USP10 | GRCh38.p7 | 16:84772520 | CAGGGACGGTGTGTC[C/T]TGGTGTGCTTTGTGT | 9100 |
| rs769138888 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84763485 | CTGAATGATTCAAAG[G/T]TAAGTTGCAGCTAAC | 9100 |
| rs769164607 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84754135 | CACACAGCACTAATA[C/T]CAGGTAGGCAGTGAT | 9100 |
| rs769191472 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84725651 | TCAGGTGATCCACCC[A/G]CCTCGGCCCCCCAGA | 9100 |
| rs769195477 | snp | C/T | 3.31214e-05 | 0.00406935 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84772609 | GCACCTGAAACGATT[C/T]GTTTATGAGAAGACT | 9100 |
| rs769204828 | in-del | -/A | | | intron-variant | USP10 | GRCh38.p7 | 16:84735293 | ACATCACACTGATGT[-/A]AACCATACGTTTTAG | 9100 |
| rs769206686 | snp | C/T | | | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84760254 | ACTCCTGACAGTTAA[C/T]AAGTCAAGCCTGTCT | 9100 |
| rs769209411 | snp | C/G | 1.66142e-05 | 0.00288216 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744837 | ACTGCCAGTACCCAG[C/G]CTCTGCCCTCGCTTT | 9100 |
| rs769222256 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84737661 | CTGGTGGTCGTCTCA[C/G]CAGATCCCTGCTGTG | 9100 |
| rs769263285 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84746756 | GGCTGTACTACGTTG[A/G]TTTACAAATTTTTCC | 9100 |
| rs769274672 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84713294 | GTCTGTAGACAGGCT[C/T]GCCCCCTTTGTCCCT | 9100 |
| rs769344332 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84705581 | GCTGACTCCTCCCTC[C/T]GTCCCTTTCCCTCTT | 9100 |
| rs769353453 | snp | A/C | 1.65894e-05 | 0.00288 | missense, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779050 | GAACGCACAGCCTAC[A/C]TCCTGTATTACCGCC | 9100 |
| rs769369289 | snp | A/C/T | 3.37628e-05 | 0.00410859 | intron-variant | USP10 | GRCh38.p7 | 16:84762959 | ACAGTGATCAGTTCA[A/C/T]AGTAACGTGATTATA | 9100 |
| rs769371910 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84740079 | TTTGGCTTCATTTTC[C/G]GATCTGTTTAATAGT | 9100 |
| rs769376538 | snp | A/G | 0.000112254 | 0.00749097 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745613 | GTTTCTGAAAAGCAG[A/G]TTGAAGTCAAAGAAG | 9100 |
| rs769389801 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84772239 | TATTTTTAGTAGAGA[C/T]GGGATTTCACCATGT | 9100 |
| rs769414950 | snp | A/C/G | 0.000166353 | 0.00911877 | intron-variant | USP10 | GRCh38.p7 | 16:84733544 | GTCCGTGGGTAGATA[A/C/G]AATTAATAGTTATGT | 9100 |
| rs769436378 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84760927 | ATGTATTCAGAGAGA[A/C]AAATAGTTGAGAAAA | 9100 |
| rs769499295 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84715090 | TGCACCACCATGCCT[A/G]GCTACTTTTTATATT | 9100 |
| rs769517916 | snp | C/T | 1.65773e-05 | 0.00287895 | intron-variant | USP10 | GRCh38.p7 | 16:84759882 | TTAACATTTTTTCCC[C/T]ATGTTTAGTGTTCGG | 9100 |
| rs769567888 | snp | G/T | 3.28996e-05 | 0.0040557 | intron-variant | USP10 | GRCh38.p7 | 16:84760278 | CCTGTCTGAAAAGGT[G/T]TGAGACTTCTCTGTT | 9100 |
| rs769583103 | snp | C/T | 1.66001e-05 | 0.00288094 | synonymous-codon, nc-transcript-variant, intron-variant | USP10 | GRCh38.p7 | 16:84759470 | ACCCATGATAGACAG[C/T]TTGTAAGTAAGGTGG | 9100 |
| rs769613226 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84758578 | ACTGAATGAAGCCTT[A/T]ACAGTATGCATTTTC | 9100 |
| rs769646363 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84761527 | TTCCAGACTCCTCTC[A/C]CAGTGGGGCCACAAG | 9100 |
| rs769682546 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84700938 | CCGCCATTATAATTA[C/T]TCTGGACAAAAATCG | 9100 |
| rs769707174 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84752969 | TTTTTTAAAAACGTA[-/T]TTTTTTTTTTCTTAA | 9100 |
| rs769716926 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84736372 | GCGCCTCCTGCCAGC[A/G]GAGGGCTGCTTTGTC | 9100 |
| rs769730257 | snp | A/G/T | 3.43096e-05 | 0.00414172 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779105 | GTGCGCTGTGTGTGC[A/G/T]CCCAGTGCCCGCTTC | 9100 |
| rs769741120 | snp | C/T | 1.66854e-05 | 0.00288833 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744892 | GGAAGTTTTGGAAAA[C/T]GATGGTGTCTCAGGT | 9100 |
| rs769779915 | snp | A/T | 3.32491e-05 | 0.00407719 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764234 | TTTTGTTCAGACTCC[A/T]ATCACCGGCATTTTT | 9100 |
| rs769815670 | snp | G/T | 2.49747e-05 | 0.00353366 | intron-variant | USP10 | GRCh38.p7 | 16:84778855 | AATGATTCGTGTGCA[G/T]TGCTGTTCTCACTCT | 9100 |
| rs769837533 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84753307 | ATGTTTAAAACTTGT[C/T]AAGATTTTAAGGAAG | 9100 |
| rs769880072 | snp | C/G/T | 9.94158e-05 | 0.00704975 | intron-variant | USP10 | GRCh38.p7 | 16:84775241 | GTGAGTAAATTTGTA[C/G/T]GACATTACTTCTTCA | 9100 |
| rs769936316 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84735033 | TTTCTATTTTTTCTT[A/T]TCTTTTCTTTTTTTC | 9100 |
| rs769936956 | snp | A/C | 3.31499e-05 | 0.0040711 | intron-variant | USP10 | GRCh38.p7 | 16:84740393 | GTTCTCTCCTTATTT[A/C]CCTGAAGGGAATTTG | 9100 |
| rs769942153 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84730457 | AAACACGCTTAAAAT[C/G]TATAACATTTTCTCA | 9100 |
| rs769979292 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84756271 | AGCAGGGGTTTACTC[A/G]CCTTCAGCGAAAGGC | 9100 |
| rs770025636 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84776854 | GTTTTGCTCTGTCGC[C/T]CAGGCTGGAGTGCAG | 9100 |
| rs770050084 | in-del | -/TG | | | intron-variant | USP10 | GRCh38.p7 | 16:84765258 | TCACAGTTACCCTTG[-/TG]TGTGTGTGTGTGCAC | 9100 |
| rs770054314 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84711517 | TGCTCTCTTTTGCTG[G/T]TGTTGCTCATGGATT | 9100 |
| rs770087662 | snp | C/T | 1.65625e-05 | 0.00287766 | missense, nc-transcript-variant, intron-variant | USP10 | GRCh38.p7 | 16:84758755 | TCCATAAACCAGTGT[C/T]GTTGCAACCCCGTGG | 9100 |
| rs770094010 | in-del | -/TA | | | intron-variant | USP10 | GRCh38.p7 | 16:84763410 | TATACACACACTGTG[-/TA]TATATATATATATGT | 9100 |
| rs770128115 | snp | A/T | 1.69559e-05 | 0.00291164 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745312 | CTGCGTTGGTACCGA[A/T]ACTACTGAAAACCTT | 9100 |
| rs770139727 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84778447 | CATTTCTTCTAGTGG[C/T]TATTGAGGTTTTCCG | 9100 |
| rs770184850 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84733154 | ATAAAAATCTCCTGC[A/C]AGCAGGACTCGACAA | 9100 |
| rs770188032 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84733858 | TCACCATAGTCAATC[A/G]TAGTGTTTTATGTGC | 9100 |
| rs770189350 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84775551 | TTGTGGCACCTGTGG[G/T]TGACAGTGCTGTGGA | 9100 |
| rs770227735 | snp | A/C | 5.03977e-05 | 0.00501959 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745090 | TGACATGCCCCCGTC[A/C]GTTACGCCCAGGACT | 9100 |
| rs770236575 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84759215 | CCTAGTAACTATTTG[A/G]TTTATTCCTTTTCGT | 9100 |
| rs770238126 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84725738 | ACCCGTGTTTCTTAA[C/T]CCTTTTTAGATCCAA | 9100 |
| rs770253206 | in-del | -/TAAT | | | intron-variant | USP10 | GRCh38.p7 | 16:84731736 | GTGATTTAAAATTAG[-/TAAT]TAATTTCCGCGAACA | 9100 |
| rs770270424 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84743627 | AAATATAAGGCATGT[A/G]TCCTTCCCTTAACTT | 9100 |
| rs770278823 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84706639 | TCCGCCTCCCGGGTT[C/G]ACGCCATTCTCCTGC | 9100 |
| rs770279842 | in-del | -/GTG | | | intron-variant | USP10 | GRCh38.p7 | 16:84770203 | TCTGGGTGCGTGGTT[-/GTG]GTGGTGTGTTACCAG | 9100 |
| rs770283852 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84771799 | TTTGAACCCGGGAGA[C/T]GGATGTTGCAGTGAG | 9100 |
| rs770284234 | snp | A/G | 0.000120344 | 0.00775613 | intron-variant | USP10 | GRCh38.p7 | 16:84745717 | TGAAGATGGGAGCAG[A/G]CCTCATCAACTGGGC | 9100 |
| rs770285845 | snp | A/G/T | 4.35021e-05 | 0.00466364 | intron-variant | USP10 | GRCh38.p7 | 16:84764071 | AGTAGTGTAAGCAGA[A/G/T]GCTCTCCTTTTCAGA | 9100 |
| rs770290321 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84768538 | AAACGTGATCCCAAG[C/G]GCCTCTTTTAGCTCT | 9100 |
| rs770301094 | snp | G/T | 2.62622e-05 | 0.00362359 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84760193 | GAGATAAAATCGTGA[G/T]GGATATTCGCCCTGG | 9100 |
| rs770335149 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84772489 | GTGGATGTGGTGTTA[C/G]CTGTTGCAAGTAAGA | 9100 |
| rs770340975 | snp | C/T | 5.59143e-05 | 0.00528716 | intron-variant | USP10 | GRCh38.p7 | 16:84768368 | CAAGAGGTATGTTCA[C/T]ACTTGATTTTGAACC | 9100 |
| rs770369481 | in-del | -/T | 1.65831e-05 | 0.00287945 | intron-variant | USP10 | GRCh38.p7 | 16:84759873 | CTGCACTATTTAACA[-/T]TTTTTCCCCATGTTT | 9100 |
| rs770371547 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717948 | TTTGGGATTCGTGAT[C/T]ACGTTAGGGTATTTG | 9100 |
| rs770384433 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84727946 | TAGAATTTTCCCTTC[C/T]AGCACAGGATCCAGT | 9100 |
| rs770384593 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84724390 | AAACCATACTTTGAG[A/T]GGTAAAATGATTACT | 9100 |
| rs770390794 | snp | C/T | 3.36859e-05 | 0.00410388 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745448 | GAGAGTGCATCACCT[C/T]CTGCTGACGGCACGG | 9100 |
| rs770435209 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84753241 | CCTGCCATAGCCTCC[C/G]AAAGTGTTGCCTGAA | 9100 |
| rs770437207 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745461 | CTCCTGCTGACGGCA[C/G]GGGCTCTGCATCAGG | 9100 |
| rs770461081 | in-del | -/AGGGGTT | 1.65869e-05 | 0.00287979 | intron-variant | USP10 | GRCh38.p7 | 16:84775272 | TTAAAACACTGATGA[-/AGGGGTT]TACAGCTGGGCACAG | 9100 |
| rs770547951 | snp | A/G | 0.000149366 | 0.00864065 | missense, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84733480 | TTCAATCAATTCTTT[A/G]TGACTCCTCGATCTT | 9100 |
| rs770549177 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84735815 | AGGGGTATAAAAAGA[C/G]TTTATCAAAATCACA | 9100 |
| rs770589245 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84768101 | GTGATATTGAATAAT[C/G]TTATTTTCAGTGTTT | 9100 |
| rs770618005 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84721359 | ACTGAGGAATTATTC[G/T]TCTGTAAATGAAAGA | 9100 |
| rs770632826 | snp | A/G | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698688 | GCAACCTCCGTCTCC[A/G]GGGTTCAAGTGATCC | 9100 |
| rs770681243 | snp | C/T | 3.31813e-05 | 0.00407302 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764215 | CCGTCACCCGCCAGG[C/T]GGATTTTGTTCAGAC | 9100 |
| rs770706175 | in-del | -/CTTT | | | intron-variant | USP10 | GRCh38.p7 | 16:84732444 | TGACTTCTTCTTCTT[-/CTTT]TTTTTTTTTTTCTTT | 9100 |
| rs770708347 | snp | A/G | 1.65732e-05 | 0.00287859 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764172 | AGCGAGGATGAATGG[A/G]AACAAGTGGGCCCCC | 9100 |
| rs770711762 | in-del | -/TC | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698599 | CTTTCTTTCTTTCTT[-/TC]TTTTTTTTTTTTTGA | 9100 |
| rs770764632 | snp | A/G | | | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84760262 | CAGTTAACAAGTCAA[A/G]CCTGTCTGAAAAGGT | 9100 |
| rs770784097 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84776487 | CGGCCATGGGCACCA[C/T]GCGCTTGTGGGTGTC | 9100 |
| rs770881515 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84743031 | CACATGGAGCCTTCC[A/G]CCCCAGGCACACCCG | 9100 |
| rs770889973 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84768956 | TCAGTTGGGCGAGAC[A/G]GATAGCATTCTGCCC | 9100 |
| rs770891908 | snp | C/T | 1.78777e-05 | 0.00298974 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745541 | TCTAAGCCCTCTTCC[C/T]CCTCGCCGGTGGCCT | 9100 |
| rs770912717 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84708646 | TTTTGTCTTCTGTCA[C/T]TTTGTTTCATCAGAG | 9100 |
| rs770923415 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84741888 | AGGATCCATTTCTCT[C/G]TGTCTGTCACTGCGC | 9100 |
| rs770958313 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84771726 | ATACAAAATTAGCCA[G/T]ATGTGGTGGTGGGAG | 9100 |
| rs771008606 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84751115 | TGGAGCTAAACAATT[G/T]CTAGTGACCAGTGAG | 9100 |
| rs771019821 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84736605 | TGTTATTTATGTTCA[A/G]AAAGAAAGAGAAAAT | 9100 |
| rs771046313 | snp | G/T | 1.65864e-05 | 0.00287974 | intron-variant | USP10 | GRCh38.p7 | 16:84775143 | GTGCTTCAAGCCATT[G/T]ATATTTTGTTTTCCA | 9100 |
| rs771061698 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84743502 | TATTCAGTTCTCCGC[A/C]GTAGAACACCGTTCT | 9100 |
| rs771061712 | snp | G/T | 1.66549e-05 | 0.00288568 | intron-variant | USP10 | GRCh38.p7 | 16:84740264 | GGTAAGCGTTGGTTT[G/T]AACATTTTGTTGAAT | 9100 |
| rs771073692 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84711460 | GTCAACATCTCTGAG[A/G]ATGTGTGCATAGCAT | 9100 |
| rs771074786 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84737046 | GCCCGCCTCGGCTTC[C/T]CAAAGTGCTGGGATT | 9100 |
| rs771080550 | snp | C/T | 1.73177e-05 | 0.00294254 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745243 | TTTTGGTCAGTCCTG[C/T]TTCCCTGCAGAGGCT | 9100 |
| rs771119942 | snp | C/G | 0.000143051 | 0.00845607 | utr-variant-5-prime, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84700055 | AAGCAGCGTGAGCAG[C/G]CGGAGGATCGCGGAG | 9100 |
| rs771122500 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84763328 | AGCCTATAAAAAAGC[C/T]GAAAGAATCGTTTGA | 9100 |
| rs771133784 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717273 | GGGCCTAATTCCCTT[A/T]CATCAGTTTCTCGGG | 9100 |
| rs771170337 | snp | A/G | 1.70229e-05 | 0.00291739 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745307 | CAGCCCTGCGTTGGT[A/G]CCGATACTACTGAAA | 9100 |
| rs771180123 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84745039 | CAATTCAGCAGTCCC[A/G]AACAGTGTCAGTGCA | 9100 |
| rs771237238 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84738472 | ACGAGATGGAGGCTT[C/G]CTGAGACACACATGG | 9100 |
| rs771276752 | snp | C/G | 0.000215405 | 0.0103757 | missense, nc-transcript-variant, intron-variant | USP10 | GRCh38.p7 | 16:84759445 | AAGTGCAAAGGCCTT[C/G]TACGTCAACACCCAT | 9100 |
| rs771280156 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84733005 | ACATTTTCCTTTTTT[C/G]GATTTCCTTGTCTTC | 9100 |
| rs771300776 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84739691 | TGAGATAACCTTTCA[C/G]CTTTTTACAAAGAAG | 9100 |
| rs771308500 | snp | A/T | 6.62723e-05 | 0.00575602 | missense, intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84740367 | TGGATAAACTACCTG[A/T]TGGTAAGCTAGTTCT | 9100 |
| rs771335105 | snp | A/C | 1.67649e-05 | 0.0028952 | intron-variant | USP10 | GRCh38.p7 | 16:84762979 | ACGTGATTATATTTG[A/C]CCTTTTCAGGGTCGA | 9100 |
| rs771340578 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84713908 | TGCCGTGTCGCTGAA[A/G]TGCATTTGGGACGTG | 9100 |
| rs771357079 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84702986 | CGACAGAGCAAGACT[C/T]CCGTCTCAAAAAAAA | 9100 |
| rs771370425 | snp | A/G | 3.93244e-05 | 0.00443403 | intron-variant | USP10 | GRCh38.p7 | 16:84745694 | GTTGAAAAGATACAA[A/G]TCTAGAGTGAAGATG | 9100 |
| rs771370654 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84757340 | GAAATTATTCCCTAC[A/G]CTTCTTCAGTTAGAA | 9100 |
| rs771382548 | snp | A/G | 1.73357e-05 | 0.00294407 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779112 | GTGTGTGCGCCCAGT[A/G]CCCGCTTCGTAGGAC | 9100 |
| rs771394088 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84704989 | CCAGCACCTGCTACC[A/G]TCTGCGCTGTAATGG | 9100 |
| rs771416056 | in-del | -/TG | 1.69733e-05 | 0.00291314 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779096 | AAACCCTGTGTGCGC[-/TG]TGTGTGCGCCCAGTG | 9100 |
| rs771420751 | snp | C/T | 3.35329e-05 | 0.00409455 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745083 | TTATGGGTGACATGC[C/T]CCCGTCAGTTACGCC | 9100 |
| rs771428057 | in-del | -/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84777089 | TTACCTGTAGAGTGA[-/G]CAAAGGAACACTTTT | 9100 |
| rs771433494 | snp | A/G | 0.00024303 | 0.0110207 | intron-variant | USP10 | GRCh38.p7 | 16:84768361 | AACCAAACAAGAGGT[A/G]TGTTCACACTTGATT | 9100 |
| rs771438570 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84758411 | ATCTATTCTCTAATA[A/G]TGATACTGTGTTAAC | 9100 |
| rs771498751 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84751996 | TGATTTGTGGCAGCC[C/T]TTGTGAGCTACCATC | 9100 |
| rs771503999 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84724865 | GTGTCATCTCCAGAT[A/G]TCCTCAGAACCACCC | 9100 |
| rs771511122 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84734886 | GCCTCCTCACCATTC[A/G]TTGGGAACTCGGCCC | 9100 |
| rs771514873 | in-del | -/ATTCCCTTT | | | intron-variant | USP10 | GRCh38.p7 | 16:84749254 | GATCCACTACCACAA[-/ATTCCCTTT]AGTGGGCACACTTTT | 9100 |
| rs771566103 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84727236 | AAAACTAATTCATGT[C/T]ATCAGTGGCATTTCC | 9100 |
| rs771571955 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84760833 | GGCCGCCCTTAGCAC[C/T]GTTAACTGGAGCATT | 9100 |
| rs771588695 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84700198 | CGTCCGCGCCCTGCC[C/G]GGAGCGAGCGTGTGG | 9100 |
| rs771602135 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84726465 | CCCAGGGTTTCTCAA[C/G]TCAGGCCCCCTGAGG | 9100 |
| rs771606578 | snp | C/T | 3.31433e-05 | 0.0040707 | intron-variant | USP10 | GRCh38.p7 | 16:84759979 | TTGTTGATGCTATTA[C/T]ATATTGGGAGTTATG | 9100 |
| rs771613014 | snp | C/T | 0.000132503 | 0.00813842 | missense, nc-transcript-variant, intron-variant | USP10 | GRCh38.p7 | 16:84758734 | TGCTGGAGAATGTAA[C/T]CCTAATCCATAAACC | 9100 |
| rs771646820 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779297 | TGGTTGAAACAGACT[A/G]TTGCTTGATTTTAGA | 9100 |
| rs771647020 | snp | C/G | 0.000310029 | 0.0124466 | intron-variant | USP10 | GRCh38.p7 | 16:84732471 | TTTCTTTTTGAGATG[C/G]AGTCTGGCTCTGTCG | 9100 |
| rs771650508 | snp | A/T | 1.65877e-05 | 0.00287986 | intron-variant | USP10 | GRCh38.p7 | 16:84772504 | GCTGTTGCAAGTAAG[A/T]CAGGGACGGTGTGTC | 9100 |
| rs771683595 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84741453 | TGCACGTGGTGAGCA[C/T]GCTGCTCATGTTGAA | 9100 |
| rs771736831 | snp | A/T | 1.67694e-05 | 0.00289558 | intron-variant | USP10 | GRCh38.p7 | 16:84733389 | TTTCTGAAAGTATAT[A/T]ATTTGTATATTTTAT | 9100 |
| rs771737836 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84755046 | GCAGCCAGTTCTTGA[A/T]GGCTGTGCAATGCTT | 9100 |
| rs771765626 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84707904 | GGCAACGTAGCAAAA[C/G]TCTTTCTCTACAAAA | 9100 |
| rs771784330 | snp | A/C/G | 5.03506e-05 | 0.00501729 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745441 | CAAACCCGAGAGTGC[A/C/G]TCACCTCCTGCTGAC | 9100 |
| rs771805162 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84722353 | TTGATAGACATTTTT[A/G]TTGTTCCCACTGTTT | 9100 |
| rs771842874 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779898 | AGTTGTCGCCCATCA[A/G]TAAAAATCACAAAGT | 9100 |
| rs771856395 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84715363 | TAAGGCATAAGAAAC[A/G]ACTGGGCACGTTACA | 9100 |
| rs771946842 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84765595 | TTCCTGTTGTGGCAA[A/G]TGGCAGGGTCTTTAT | 9100 |
| rs771949604 | snp | C/T | 2.20078e-05 | 0.00331714 | intron-variant | USP10 | GRCh38.p7 | 16:84778879 | TCACTCTGCTGCCTG[C/T]TGGGCTCTCTTCCAG | 9100 |
| rs771980758 | snp | A/G | 1.66721e-05 | 0.00288717 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745385 | ACAGCTACCAACGGG[A/G]TGGAGTTGCACACCA | 9100 |
| rs771982379 | snp | C/T | 5.55247e-05 | 0.00526871 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84760188 | TCTTGGAGATAAAAT[C/T]GTGAGGGATATTCGC | 9100 |
| rs771999861 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84722819 | CCTCGGCCTCCCAAA[G/T]TGCTGGGATTACAGG | 9100 |
| rs772009565 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780313 | GAAGCCTTCTGAGAC[A/G]GAAGACATGGAGAGA | 9100 |
| rs772037438 | snp | C/T | 1.85183e-05 | 0.00304283 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764088 | CTCTCCTTTTCAGAA[C/T]TTACGATTTCCAACG | 9100 |
| rs772041091 | snp | A/G | 3.33751e-05 | 0.0040849 | missense, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84778964 | TCCAGATCGGTCTGA[A/G]TGGCTGGCTGCGCAT | 9100 |
| rs772073078 | snp | C/T | 1.65688e-05 | 0.00287821 | missense, nc-transcript-variant, intron-variant | USP10 | GRCh38.p7 | 16:84759427 | TCATTCCTCTGTATT[C/T]CAAAGTGCAAAGGCC | 9100 |
| rs772111294 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84749811 | CTTGATTACTCTTAA[A/G]CTATCCACTTTAACG | 9100 |
| rs772128884 | snp | C/G | 1.66059e-05 | 0.00288144 | intron-variant | USP10 | GRCh38.p7 | 16:84758856 | TTGTTGCAGCTGTCC[C/G]TCCTTTGGGTGCATG | 9100 |
| rs772164666 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84742381 | CTTTCTCTCCCCTCC[C/G]TCCATGTTTTCATTC | 9100 |
| rs772184900 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84720552 | TAAATTGAAAACAGA[A/T]GCAGAATAAAAAGAT | 9100 |
| rs772212085 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84702854 | AAAAATTAGCCGAGT[G/T]TGGTGAAGCTCGCCT | 9100 |
| rs772219659 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84742785 | GGAATCTGCCTTCTA[G/T]TGAGATGATCAAACA | 9100 |
| rs772222629 | snp | A/G | 1.72285e-05 | 0.00293495 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745172 | AGTCCTTTCCCCGGA[A/G]CACTCGGCAGTGACA | 9100 |
| rs772223597 | in-del | -/CTT | 0.0706532 | 0.174169 | intron-variant | USP10 | GRCh38.p7 | 16:84732431 | AATTCTTCTCAATGA[-/CTT]CTTCTTCTTCTTCTT | 9100 |
| rs772224057 | in-del | -/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84729335 | CAATTCTAAGAAATT[-/C]CGTTTTATTCTTAGG | 9100 |
| rs772233057 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84724796 | GATTGTTGATGCTCA[A/G]TGCATATTGTTAAAT | 9100 |
| rs772275192 | snp | C/T | 1.66172e-05 | 0.00288242 | intron-variant | USP10 | GRCh38.p7 | 16:84760292 | TTTGAGACTTCTCTG[C/T]TGTCACTAGTATCAA | 9100 |
| rs772289974 | snp | G/T | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717205 | GCTTCAGAGGGTCTG[G/T]GAAGTTCTGAAATCA | 9100 |
| rs772313745 | in-del | -/GGCTCTGCATCA | 0.000169691 | 0.00920961 | cds-indel, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745463 | CCTGCTGACGGCACG[-/GGCTCTGCATCA]GGCACCCTTCCTGTC | 9100 |
| rs772322656 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84770374 | TATTATGTTTTAGAT[C/G]AGAAGTATTTTTCTG | 9100 |
| rs772336698 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84765071 | CAGAGCAAGACTGTC[C/T]TCAAAAAAAAAAACC | 9100 |
| rs772423546 | snp | C/T | | | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719650 | AATATAGGAAGCCGA[C/T]TGGGTGGAAAACATC | 9100 |
| rs772429133 | snp | A/G | 1.65946e-05 | 0.00288046 | intron-variant | USP10 | GRCh38.p7 | 16:84775130 | AACCTTTCTAAAAGT[A/G]CTTCAAGCCATTGAT | 9100 |
| rs772432249 | snp | A/G | 1.74048e-05 | 0.00294993 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745223 | GAGGGGGGCCCCGGG[A/G]CTGATTTTGGTCAGT | 9100 |
| rs772454018 | snp | C/T | 1.65671e-05 | 0.00287807 | missense, intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84740361 | AGGCTGTGGATAAAC[C/T]ACCTGATGGTAAGCT | 9100 |
| rs772458989 | snp | A/G | 1.65608e-05 | 0.00287752 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84772616 | AAACGATTCGTTTAT[A/G]AGAAGACTGGTGGGT | 9100 |
| rs772464112 | snp | C/T | 0.000837857 | 0.0204506 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745219 | GCCAGAGGGGGGCCC[C/T]GGGGCTGATTTTGGT | 9100 |
| rs772476166 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84720337 | TGTAGAACAGATGGC[A/T]CTTACAAGTTTCTGC | 9100 |
| rs772479585 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84727900 | CCTGTCCATATTCTA[A/C]TTTTGGGAGTTGACC | 9100 |
| rs772482757 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84776806 | TGCCCTCCTGAATCC[C/T]CATCCCCTAACCCAT | 9100 |
| rs772498006 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84756410 | CCAGCCTGGCCAACA[G/T]GGTGAAATCCTGTCT | 9100 |
| rs772499140 | in-del | -/CA | | | intron-variant | USP10 | GRCh38.p7 | 16:84741716 | CTTGCCACCAGTTTG[-/CA]CAGTTAGTGACAGGC | 9100 |
| rs772521989 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84774006 | TGTAATCCCAGCACT[C/T]TGGGAGGCCGAGGCA | 9100 |
| rs772529181 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84713138 | GCCACAGTTAGTTTA[G/T]CTTTCCCCCACCTTT | 9100 |
| rs772547998 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84726523 | AAGGTAAACTGAGCC[A/G]GCTTAGCCAACAGGC | 9100 |
| rs772620116 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84710593 | TTTAAAAACAAGCAT[C/T]TGTCCCTTGATTATA | 9100 |
| rs772638525 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84739571 | AGCCACCATGCCCTG[C/T]CCCTTCCTAAACTTT | 9100 |
| rs772645905 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84752053 | AAAGGCTATTAAGCA[A/G]CTCCATTTTTCTGTA | 9100 |
| rs772650949 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84731601 | GAATTCTATGAAAAA[A/G]TACTCTGGCATTCTA | 9100 |
| rs772658760 | snp | A/G | | | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84760261 | ACAGTTAACAAGTCA[A/G]GCCTGTCTGAAAAGG | 9100 |
| rs772681170 | snp | C/G | 4.86938e-05 | 0.00493402 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84768211 | TGTGGTTTACCAGCA[C/G]AGTTCAAAAGAATCT | 9100 |
| rs772729163 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84734913 | GCCCTTAGCTGTCCT[C/G]TCAGCCCCGTTGGGC | 9100 |
| rs772753646 | snp | A/G | 1.65715e-05 | 0.00287845 | intron-variant | USP10 | GRCh38.p7 | 16:84759980 | TGTTGATGCTATTAC[A/G]TATTGGGAGTTATGG | 9100 |
| rs772772380 | snp | A/T | 6.66345e-05 | 0.00577172 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745397 | GGGGTGGAGTTGCAC[A/T]CCACGGAAAGCATAG | 9100 |
| rs772783259 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84768846 | CTGATGCTTGTTACT[C/G]TTTGATTTGATCTGG | 9100 |
| rs772796256 | snp | A/C | 1.67652e-05 | 0.00289522 | intron-variant | USP10 | GRCh38.p7 | 16:84733390 | TTCTGAAAGTATATA[A/C]TTTGTATATTTTATG | 9100 |
| rs772826928 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84707927 | CTACAAAAATACAAA[A/C]ATTCACTGGGCATGG | 9100 |
| rs772842239 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84752557 | GAAAATGTTGATGTT[C/G]AAAGAGGAATTTAAA | 9100 |
| rs772886014 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84772864 | TTCTCATGAAAATGG[C/T]CTGTTGAAAATAGAG | 9100 |
| rs772908850 | snp | C/G/T | | | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719682 | CTTCTAGTGTATGTA[C/G/T]GTCCCATAAGGGGGA | 9100 |
| rs772941960 | snp | G/T | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698244 | TCTCTCCCTGAATGT[G/T]TATGTGTGTACATGA | 9100 |
| rs772946804 | snp | C/T | 1.656e-05 | 0.00287745 | intron-variant | USP10 | GRCh38.p7 | 16:84768362 | ACCAAACAAGAGGTA[C/T]GTTCACACTTGATTT | 9100 |
| rs772959161 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84737877 | TGGTCCAGCCTTTCC[A/G]GCCTCTCCACCCTCA | 9100 |
| rs772965502 | snp | A/G | 1.65828e-05 | 0.00287943 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744759 | CTGAATTTATTCTCG[A/G]TTGTACAGCTTCCAA | 9100 |
| rs773044842 | snp | A/G | 4.99164e-05 | 0.00499557 | missense, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84778976 | TGAATGGCTGGCTGC[A/G]CATCGATGACCAGAC | 9100 |
| rs773060941 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84734080 | AAAATATTGCACTCA[A/G]TGTATTTTATCATGT | 9100 |
| rs773072305 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84748555 | GTGATCCTCCTGCCT[C/G]AGCCTCTCAAAGTGC | 9100 |
| rs773077470 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84715372 | AGAAACAACTGGGCA[C/T]GTTACAAGATGTGTA | 9100 |
| rs773122448 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84767133 | TAATTAAACCCTGGA[C/T]AGAAAAGCTTTTAGC | 9100 |
| rs773132095 | snp | C/T | 1.72285e-05 | 0.00293495 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745173 | GTCCTTTCCCCGGAG[C/T]ACTCGGCAGTGACAC | 9100 |
| rs773223229 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84742394 | CCCTCCATGTTTTCA[G/T]TCTCAGTTGTTTGTA | 9100 |
| rs773228341 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84770420 | GTTTTGGGGAAAATA[C/G]GATTATATGAAATAT | 9100 |
| rs773265361 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84741014 | GCACAATTCAAACTT[C/G]TCGAGATCATTTTTC | 9100 |
| rs773303701 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84716927 | ACGCAACTTAAAATA[A/G]AAGTCCAGAGCCATA | 9100 |
| rs773350766 | snp | C/T | 3.31906e-05 | 0.0040736 | missense, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84733493 | TTGTGACTCCTCGAT[C/T]TTCAGTTGAGGTAAG | 9100 |
| rs773357526 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84728257 | TTTAGTCAGATATCA[G/T]TTTAGTTAAATAATT | 9100 |
| rs773374157 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84709869 | TAAATTTGTGGCTGA[A/G]ATGGTGTGTAGGGTG | 9100 |
| rs773394973 | snp | C/G | 1.73972e-05 | 0.00294929 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745224 | AGGGGGGCCCCGGGG[C/G]TGATTTTGGTCAGTC | 9100 |
| rs773420242 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84742886 | TAGAATGTTTTATGT[A/T]CTGATAAGATTGAGA | 9100 |
| rs773474967 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84736566 | CCTTATTTAATAAGC[A/G]TGTTTAAACCTCAGT | 9100 |
| rs773499518 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84737150 | GAGAGTCTTTGAGAC[A/G]GAAAGCAGAACACAC | 9100 |
| rs773500318 | snp | A/G | 6.63196e-05 | 0.00575807 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764155 | AAGAACAAGGTGAAG[A/G]AAGCGAGGATGAATG | 9100 |
| rs773513600 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84762453 | CCCAGCACTTTGGGA[A/G]GCCAAGGCAGGCAGG | 9100 |
| rs773559801 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84701527 | CTTAAATCCTAATTA[A/G]CTAGCTTATTAGAAT | 9100 |
| rs773586266 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84759313 | TGTGCCTTCAGGAAA[C/T]GTGGTGTGTCTGTTC | 9100 |
| rs773593703 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84713160 | CCCACCTTTGTGACC[G/T]TAGATATCTCAGCCA | 9100 |
| rs773598217 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84753398 | AATTCATTTGCTTTT[A/C]CCTTCTCCTTCCACC | 9100 |
| rs773601127 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84777359 | ATTCTACTGATGGTC[C/G]CTTTGAAGCAAAACT | 9100 |
| rs773612895 | in-del | -/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84747770 | TGGGGTTTCACCATG[-/C]TGCCCAGGCTGGCCT | 9100 |
| rs773623146 | snp | C/T | 1.65924e-05 | 0.00288027 | intron-variant | USP10 | GRCh38.p7 | 16:84775134 | TTTCTAAAAGTGCTT[C/T]AAGCCATTGATATTT | 9100 |
| rs773688269 | snp | C/T | 8.1126e-05 | 0.00636839 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745574 | GTGGAAACTAAGTAT[C/T]CCCCTCCCGCCATAT | 9100 |
| rs773689564 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84749289 | TTTTAAGTGTAGGCC[C/T]ACTTATTTTAAGCAG | 9100 |
| rs773707467 | snp | A/G | 1.65644e-05 | 0.00287783 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84772656 | TTATCAAAAATATTG[A/G]ATATCCTGTGGACTT | 9100 |
| rs773739611 | in-del | -/GGG | 1.65699e-05 | 0.00287831 | intron-variant | USP10 | GRCh38.p7 | 16:84759974 | AGTTTTGTTGATGCT[-/GGG]ATTACATATTGGGAG | 9100 |
| rs773749826 | in-del | -/GGGCCTAGCGGTGG | | | intron-variant | USP10 | GRCh38.p7 | 16:84776301 | GGGGCCCAGGGGTGA[-/GGGCCTAGCGGTGG]GGGCCCAGGGGTGAG | 9100 |
| rs773763332 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84719082 | CAGGCATGAGCCACC[A/G]CGCCCGGCCAGTTTA | 9100 |
| rs773776632 | snp | C/T | 0.00232648 | 0.0340269 | intron-variant | USP10 | GRCh38.p7 | 16:84732448 | TTCTTCTTCTTCTTT[C/T]TTTTTTTTTTCTTTT | 9100 |
| rs773785602 | snp | A/T | 3.33483e-05 | 0.00408327 | intron-variant | USP10 | GRCh38.p7 | 16:84733552 | GTAGATACAATTAAT[A/T]GTTATGTTTCTATTT | 9100 |
| rs773799623 | snp | A/G | 4.16571e-05 | 0.00456364 | intron-variant | USP10 | GRCh38.p7 | 16:84760297 | GACTTCTCTGTTGTC[A/G]CTAGTATCAAGTGTT | 9100 |
| rs773802330 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84733290 | ACCTAGAACTCTGAG[G/T]TGCAGATCCTCTGTT | 9100 |
| rs773803729 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84749825 | AACTATCCACTTTAA[C/T]GGGTTCTACTTGGAC | 9100 |
| rs773849862 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84731617 | TACTCTGGCATTCTA[A/G]GAACAAAATCCTTTT | 9100 |
| rs773857476 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84725847 | TTTAATCATGCCAAA[C/T]AGTCTATTGCTCTTT | 9100 |
| rs773867025 | snp | C/T | 5.41375e-05 | 0.00520248 | utr-variant-5-prime, missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84700100 | GCAGCCATGGCCCTC[C/T]ACAGCCCGCAGGTAG | 9100 |
| rs773902884 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84732333 | ATTTTTATACCCAGT[A/G]CTGATCATACGTGGG | 9100 |
| rs773907712 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84751838 | TTTCAGGGATTTTCA[A/G]TGTTAATATGACCCC | 9100 |
| rs773918313 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84733967 | AAATTTGTCCTTGTT[A/C]TTTGATTTCCAGTGC | 9100 |
| rs773970233 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84715177 | TCAAGTGATCTGCCC[A/G]CCTAGGCCTCCCAAA | 9100 |
| rs773974037 | in-del | -/TGTGTGTGTGTGTGTGTGTG | | | intron-variant | USP10 | GRCh38.p7 | 16:84778093 | TTAAGTAAATAACTG[-/TGTGTGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 9100 |
| rs773974310 | snp | C/G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84705822 | CCTCCCAGATTCAAG[C/G/T]GATTCTCCTGCCTCA | 9100 |
| rs774024792 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84706951 | CATTGTAGTAGTCAT[C/G]ATTTGAAGCCTATAA | 9100 |
| rs774030552 | snp | A/G | 4.99064e-05 | 0.00499507 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764241 | CAGACTCCAATCACC[A/G]GCATTTTTGGTGGAC | 9100 |
| rs774057531 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84778555 | GTCAGCCACATCCAA[C/G]GGCATGAGCCAGGTC | 9100 |
| rs774116772 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84722165 | GGCTAAGAAAGTTTG[C/T]CTTTTCTAGAATTAC | 9100 |
| rs774133329 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84768891 | TTGAGTCTTTCAGTC[-/T]TCATGAATTTAAGAG | 9100 |
| rs774153866 | snp | C/G | 1.66977e-05 | 0.00288939 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744909 | ATGGTGTCTCAGGTG[C/G]TCTTGGACAAAGGGA | 9100 |
| rs774156524 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84728727 | CCTTTTTGTAGTTTT[A/G]TCAGCATATGCAAAA | 9100 |
| rs774162736 | snp | C/T | 1.6696e-05 | 0.00288924 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745381 | GGGCACAGCTACCAA[C/T]GGGGTGGAGTTGCAC | 9100 |
| rs774174565 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84710770 | TAATACCAGAATCAC[C/T]TGGCACCCTGGGTGC | 9100 |
| rs774177132 | snp | C/T | 3.38352e-05 | 0.00411296 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745317 | TTGGTACCGATACTA[C/T]TGAAAACCTTGGAGT | 9100 |
| rs774199703 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84740130 | TCTATTGTGTTTTTT[G/T]CGTTAAATGAAGATG | 9100 |
| rs774206580 | snp | C/T | 1.65737e-05 | 0.00287864 | intron-variant | USP10 | GRCh38.p7 | 16:84759888 | TTTTTTCCCCATGTT[C/T]AGTGTTCGGCTAATG | 9100 |
| rs774225463 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84766279 | ACAAGTCACTTCTGT[A/G]TTCTGCACTGTGAGC | 9100 |
| rs774257063 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84731437 | CTTCACAGCTGCCGT[C/G]TGTTTCTTGTATTTT | 9100 |
| rs774270460 | snp | G/T | 1.66161e-05 | 0.00288232 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744684 | AAGTCATTGAACCCA[G/T]TGACACTTTGCCGAG | 9100 |
| rs774271302 | snp | G/T | 1.65614e-05 | 0.00287757 | synonymous-codon, nc-transcript-variant, intron-variant | USP10 | GRCh38.p7 | 16:84758768 | GTCGTTGCAACCCCG[G/T]GGGCTGATCAATAAA | 9100 |
| rs774287245 | snp | G/T | 1.65748e-05 | 0.00287874 | intron-variant | USP10 | GRCh38.p7 | 16:84775258 | ACATTACTTCTTCAT[G/T]AAAACACTGATGAAG | 9100 |
| rs774347684 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84749154 | GGAGAATGGCATTGT[G/T]TGAAATTTTTTTTGT | 9100 |
| rs774424820 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84741638 | TTCTTGGCCCTTTTT[C/T]TCCATTCTTTACTCT | 9100 |
| rs774443477 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84737074 | ATTACAGGCGTGAGC[C/T]ACCACGCCCGGCCTA | 9100 |
| rs774453217 | snp | A/G | 3.31603e-05 | 0.00407174 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744748 | CCCTCAGGCCCCTGA[A/G]TTTATTCTCGGTTGT | 9100 |
| rs774463884 | in-del | -/CTTTTTTTTT | | | intron-variant | USP10 | GRCh38.p7 | 16:84711719 | GTGAGGAAGGGCTAG[-/CTTTTTTTTT]TTTTTTTTTTTTTGT | 9100 |
| rs774470578 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84703717 | TTTAAGTTTGTGAGC[C/T]AGTGGTCACCTTAGT | 9100 |
| rs774478549 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84775634 | GGTGATCCCTGCGTC[A/C]TCCCCCACAGGTATT | 9100 |
| rs774556143 | snp | C/G | 4.97508e-05 | 0.00498728 | intron-variant | USP10 | GRCh38.p7 | 16:84758839 | CCGTCCGCAAGGCCA[C/G]CTTGTTGCAGCTGTC | 9100 |
| rs774557010 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84778199 | CCATCTCCGCAGTGC[C/T]CCACCACAGCTCCAC | 9100 |
| rs774568358 | in-del | -/T | | | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84720076 | GGAAGGAGAGGAGTC[-/T]TATTTACCAGCTAAT | 9100 |
| rs774568908 | snp | A/G | 3.31214e-05 | 0.00406935 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84772610 | CACCTGAAACGATTC[A/G]TTTATGAGAAGACTG | 9100 |
| rs774571157 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84761486 | CAGGAAGGGAAAGGA[C/G]AGGTGAGGCAGGGCC | 9100 |
| rs774578250 | snp | A/G | 5.00856e-05 | 0.00500403 | intron-variant | USP10 | GRCh38.p7 | 16:84763112 | TGGTCCACTTGCCGC[A/G]GAGTTGTGCAAGAGT | 9100 |
| rs774599561 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84711913 | TTAGCAGAGACGGGG[C/T]TTCACCATGTTGGCC | 9100 |
| rs774622847 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84716889 | ACTCTGAGATATGCC[G/T]CTAATTTGGATGATA | 9100 |
| rs774648210 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84763496 | AAAGTTAAGTTGCAG[C/G]TAACAGTTTAGTTCA | 9100 |
| rs774651498 | snp | C/T | 3.31939e-05 | 0.0040738 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84733485 | TCAATTCTTTGTGAC[C/T]CCTCGATCTTCAGTT | 9100 |
| rs774653195 | snp | C/G | 9.52472e-05 | 0.00690033 | intron-variant | USP10 | GRCh38.p7 | 16:84778869 | AGTGCTGTTCTCACT[C/G]TGCTGCCTGCTGGGC | 9100 |
| rs774669506 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84769118 | GATGAATGCAGGCTG[A/G]TAATTATGGACGGTC | 9100 |
| rs774674567 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84742255 | CACTCCTTCACCCTG[C/T]CCTTAGCAATTCAGT | 9100 |
| rs774701008 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84701190 | ACACCTCTTTTGAAA[C/G]ATGATTTTCGGAACT | 9100 |
| rs774720274 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84760947 | AGTTGAGAAAATGCC[A/T]TTTAAGTCAAGTTTA | 9100 |
| rs774793873 | in-del | -/GTTT | | | intron-variant | USP10 | GRCh38.p7 | 16:84739253 | TTTAGTAGAGACAGG[-/GTTT]GTTTTTTTTTTGTTT | 9100 |
| rs774802174 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84737214 | TTCCTATAGCCACGG[G/T]CCCAGGTATCCTTTT | 9100 |
| rs774805488 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84770627 | AATACAAAAAGTTAG[C/G]CGGGCATGGTGGCAG | 9100 |
| rs774806258 | in-del | -/CATT | | | intron-variant | USP10 | GRCh38.p7 | 16:84709032 | CAACATAGTCAAGAA[-/CATT]CATTCATTCGTTTGT | 9100 |
| rs774819012 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84755292 | CTTTCCTTCCGTATC[A/G]TCAAGAAAACTGAAG | 9100 |
| rs774837959 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84707761 | ATAACATGTTGTCCA[A/G]ACAATTTTTTTTTTT | 9100 |
| rs774842314 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84773466 | CCTTCCATATAGATG[A/G]CCCAGGAACTGTGGG | 9100 |
| rs774851664 | snp | C/T | 3.44685e-05 | 0.00415127 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745168 | TGACAGTCCTTTCCC[C/T]GGAGCACTCGGCAGT | 9100 |
| rs774869999 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84756347 | CCTGTAATCCAAGCA[C/G]TTTGGGAGACCAAGG | 9100 |
| rs774898955 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84735383 | GAGTAGACAAAAACT[G/T]GAGTTTTCATGTGAT | 9100 |
| rs774929185 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84703200 | AACTTTAACAGTTGA[A/G]GTGTAGGTCCAAGTG | 9100 |
| rs774930646 | snp | A/G | 3.33778e-05 | 0.00408507 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744894 | AAGTTTTGGAAAATG[A/G]TGGTGTCTCAGGTGG | 9100 |
| rs774942346 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718361 | TTGGCTCAAGGGATC[A/C]TCCCACCTCAGCCTC | 9100 |
| rs775036806 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84759237 | CCTTTTCGTGGTGAC[A/G]TATCTAAGTAGTTCA | 9100 |
| rs775042664 | snp | C/G | 1.66241e-05 | 0.00288302 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744845 | TACCCAGGCTCTGCC[C/G]TCGCTTTGGATGGAA | 9100 |
| rs775106961 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84721503 | AATACAATAAATGTA[C/T]CCATTTTAAGTTTGC | 9100 |
| rs775108895 | snp | A/G | 1.88049e-05 | 0.00306629 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745623 | AGCAGGTTGAAGTCA[A/G]AGAAGGGCTTGTTCC | 9100 |
| rs775126873 | snp | C/T | 1.72856e-05 | 0.00293982 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745261 | CCCTGCAGAGGCTGG[C/T]AGAGACACCCTGTCA | 9100 |
| rs775132597 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84766137 | CTCAGTTCTGAGACT[G/T]AATCAACAACTTTCA | 9100 |
| rs775135418 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84752674 | ATTCATTCACTTGAA[C/G]ATAATTCGGTCTGGT | 9100 |
| rs775136617 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84705582 | CTGACTCCTCCCTCC[A/G]TCCCTTTCCCTCTTT | 9100 |
| rs775172894 | snp | A/G | 1.65803e-05 | 0.00287922 | missense, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84778997 | ATGACCAGACAGTCA[A/G]GGTGATCAACCAGTA | 9100 |
| rs775174729 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84733183 | AAGTTTGGCATACAA[A/T]ATTGATTTGTTTCAA | 9100 |
| rs775187567 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84758664 | TGAAATGATTTGAAT[G/T]TTCTTCACTAGATGT | 9100 |
| rs775216968 | snp | A/G | 1.697e-05 | 0.00291285 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745463 | CCTGCTGACGGCACG[A/G]GCTCTGCATCAGGCA | 9100 |
| rs775219012 | snp | A/C | 3.36649e-05 | 0.0041026 | intron-variant | USP10 | GRCh38.p7 | 16:84760281 | GTCTGAAAAGGTTTG[A/C]GACTTCTCTGTTGTC | 9100 |
| rs775240077 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84708883 | ACAGATTTTGGTGGC[C/T]GGACGTTAGGAGTAT | 9100 |
| rs775242401 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717168 | CCTCACTTTGAGTAG[C/G]AGGTCGTATTGGGCT | 9100 |
| rs775260912 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84753330 | TAAGGAAGTTGGGCT[A/G]ACATTTCCTCTTGGG | 9100 |
| rs775293690 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84709729 | CAAAGCTGGGAAGAC[A/G]TCTCTTGTAGAACGG | 9100 |
| rs775310597 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84735902 | CCCAATCTTCAGGAA[C/T]CTGAATTATAATAGC | 9100 |
| rs775313043 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84746201 | AGCCCAAAGTTAATG[-/T]TTTATTTTAGAGTGC | 9100 |
| rs775319584 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84746778 | AATTTTTCCTCAATA[A/G]GAAATTAACCTTAAC | 9100 |
| rs775335322 | snp | A/G/T | 3.31533e-05 | 0.00407134 | intron-variant | USP10 | GRCh38.p7 | 16:84759883 | TAACATTTTTTCCCC[A/G/T]TGTTTAGTGTTCGGC | 9100 |
| rs775385549 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84701116 | ATTGCGAGTAAAATC[A/G]TAACCCTTCATGAGC | 9100 |
| rs775414852 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84752721 | ACTGCTTTTGCACCC[C/G]TGTTTTTTTCACTGC | 9100 |
| rs775422779 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84774678 | GGTTTCACTGTATTA[A/G]CCAGGATGGTCTCGA | 9100 |
| rs775422973 | snp | A/G | 1.69487e-05 | 0.00291103 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745313 | TGCGTTGGTACCGAT[A/G]CTACTGAAAACCTTG | 9100 |
| rs775440173 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84730459 | ACACGCTTAAAATCT[A/G]TAACATTTTCTCAGA | 9100 |
| rs775470365 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84709618 | TCCTTGGACTTTTGA[C/T]TCGGAGGGTGCCGTG | 9100 |
| rs775476156 | snp | C/G | 0.000129576 | 0.00804805 | intron-variant | USP10 | GRCh38.p7 | 16:84745699 | AAAGATACAAATCTA[C/G]AGTGAAGATGGGAGC | 9100 |
| rs775493185 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84755118 | TTGAGTCTGTTCGAA[C/T]GGGTCAACAACGAAG | 9100 |
| rs775550288 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84748583 | TGCTGAGATTACAGG[C/T]GTGAGCCACCGCGCC | 9100 |
| rs775555580 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84722497 | TCAAAGCGGCCATGC[C/T]GTTTTCTATCTGCAC | 9100 |
| rs775571635 | in-del | -/TTCT | 0.00319999 | 0.0398717 | intron-variant | USP10 | GRCh38.p7 | 16:84732442 | AATGACTTCTTCTTC[-/TTCT]TTTTTTTTTTTTTCT | 9100 |
| rs775586782 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84729671 | TAAAATCGAAAGGAC[C/T]GGTTTTAAATATTGC | 9100 |
| rs775614978 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84767773 | TCAGCAGAATTATTA[-/T]TTATTTTTTTTAATT | 9100 |
| rs775624211 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84720767 | TTTGTATTTTTTAAT[A/G]GAGACGGGGTTTCAC | 9100 |
| rs775628441 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84728629 | CCACCGTGTCCGGCC[C/T]CCTTTTGTAGTTTTA | 9100 |
| rs775659965 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84756279 | TTTACTCGCCTTCAG[A/C]GAAAGGCAGCATGTT | 9100 |
| rs775663135 | snp | A/C/G | 3.34405e-05 | 0.00408893 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744665 | ATTGAGTTTGGTGTC[A/C/G]ATGAAGTCATTGAAC | 9100 |
| rs775681132 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84725773 | TCCTTTTGGAGATGG[G/T]AAGAATTTTAGAAGT | 9100 |
| rs775705543 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84778464 | ATTGAGGTTTTCCGT[A/T]TTTTCACTGTTATAA | 9100 |
| rs775726335 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718043 | ATGATGAGAGAGAGA[C/T]TGGGAGATTACTTGT | 9100 |
| rs775742900 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84702835 | CTGTCTCTACTAAAA[A/G]TACAAAAATTAGCCG | 9100 |
| rs775743453 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84723051 | CTTCACACTGGAAAC[C/T]GGTGGTCTTATTTGA | 9100 |
| rs775751113 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84775315 | TGCAACTTAGCATAG[C/T]GACCAGATGCTGTAC | 9100 |
| rs775785271 | snp | C/T | 1.67506e-05 | 0.00289396 | intron-variant | USP10 | GRCh38.p7 | 16:84733399 | TATATAATTTGTATA[C/T]TTTATGTGATCAGTG | 9100 |
| rs775792229 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84703561 | TTAATTCTTAAAAGA[C/G]ATACATTTTTATTAG | 9100 |
| rs775797001 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84768102 | TGATATTGAATAATC[C/T]TATTTTCAGTGTTTA | 9100 |
| rs775821553 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84759785 | ATTGGTTACCTAAAA[A/T]CTACTATACTCGTAT | 9100 |
| rs775899984 | in-del | -/TTTTTTTTT | | | intron-variant | USP10 | GRCh38.p7 | 16:84711721 | GAGGAAGGGCTAGCT[-/TTTTTTTTT]TTTTTTTTTTTTGTC | 9100 |
| rs775909301 | snp | C/T | 1.68272e-05 | 0.00290057 | intron-variant | USP10 | GRCh38.p7 | 16:84745719 | AAGATGGGAGCAGAC[C/T]TCATCAACTGGGCTT | 9100 |
| rs775930815 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84743202 | AAATAGTAGCCAAAG[A/G]AATTAGATGGTCGTG | 9100 |
| rs775931487 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84762738 | ATTTCAAAAATACAG[A/T]AAGTATAAATAATAA | 9100 |
| rs775942854 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84726035 | GGTCATAGTTGTCCA[C/G]CTGCCTCGGAAACTG | 9100 |
| rs775964757 | snp | A/G | | | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779081 | GAGTGGACCTGCTGT[A/G]AACCCTGTGTGCGCT | 9100 |
| rs776013115 | in-del | -/AA | | | intron-variant | USP10 | GRCh38.p7 | 16:84754990 | TAGACTTTGTCCCAG[-/AA]AAAAAAAAAAAGGAG | 9100 |
| rs776072893 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84754424 | ATGGCCTTTCAAAGA[C/T]TGTCAAAGGCTTGAA | 9100 |
| rs776073506 | snp | C/T | 1.79203e-05 | 0.0029933 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745543 | TAAGCCCTCTTCCTC[C/T]TCGCCGGTGGCCTAT | 9100 |
| rs776092261 | snp | C/T | 1.65715e-05 | 0.00287845 | intron-variant | USP10 | GRCh38.p7 | 16:84759983 | TGATGCTATTACATA[C/T]TGGGAGTTATGGAGA | 9100 |
| rs776128260 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718738 | TCCAGGTTGGGCAAC[A/G]GAGCAAGACTGTCTG | 9100 |
| rs776146553 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84707826 | ACTCACGCCTGTAAT[C/T]CCAGCACTTTGGGAG | 9100 |
| rs776173015 | snp | C/T | 1.65836e-05 | 0.0028795 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744769 | TCTCGGTTGTACAGC[C/T]TCCAAAATAACCCCT | 9100 |
| rs776185687 | snp | A/C | 3.38118e-05 | 0.00411154 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745455 | CATCACCTCCTGCTG[A/C]CGGCACGGGCTCTGC | 9100 |
| rs776186491 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84739737 | TCTGCTTTCTGTCTG[C/T]CAAACAAGGAATGTG | 9100 |
| rs776203211 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84710935 | TAGCAATAACGAAAT[C/T]GTATTTTGGACAAAG | 9100 |
| rs776251336 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84746704 | AGGCCCAGGACAGTA[C/T]TGAGCAAAGCCGAGT | 9100 |
| rs776330419 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84738946 | CCTGCACTGGCCTTT[A/G]TACTGCAGTGAACAG | 9100 |
| rs776358734 | snp | A/G | 3.31928e-05 | 0.00407373 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84733482 | CAATCAATTCTTTGT[A/G]ACTCCTCGATCTTCA | 9100 |
| rs776365276 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84708736 | CACATTTAAGTACTT[C/T]TGACTTGTAATAGAA | 9100 |
| rs776365907 | snp | A/G | 1.65759e-05 | 0.00287883 | intron-variant | USP10 | GRCh38.p7 | 16:84772513 | AGTAAGACAGGGACG[A/G]TGTGTCCTGGTGTGC | 9100 |
| rs776381438 | snp | A/G | 2.61005e-05 | 0.00361242 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84760194 | AGATAAAATCGTGAG[A/G]GATATTCGCCCTGGA | 9100 |
| rs776383913 | snp | C/G | 1.66153e-05 | 0.00288225 | missense, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84778981 | GGCTGGCTGCGCATC[C/G]ATGACCAGACAGTCA | 9100 |
| rs776385406 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84731646 | TTTTCTCGAAACTTT[C/G]AAAATGTTGCCCCAT | 9100 |
| rs776391974 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84780046 | GTTTGTGGAAGCTGA[A/G]CCACCACTCAGGTTA | 9100 |
| rs776414472 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84760870 | CTCCCAGATTGAGTT[G/T]GTGATGAATCAGTAC | 9100 |
| rs776415273 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84713283 | CGAGACCCTCTGTCT[C/G]TAGACAGGCTCGCCC | 9100 |
| rs776421907 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84757338 | CAGAAATTATTCCCT[A/G]CGCTTCTTCAGTTAG | 9100 |
| rs776428339 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84716827 | GGGAGTGACCGCATG[C/T]CCTGGTCTAAACTTA | 9100 |
| rs776475774 | snp | A/C | 8.28535e-05 | 0.00643583 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764175 | GAGGATGAATGGGAA[A/C]AAGTGGGCCCCCGGA | 9100 |
| rs776515543 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84752167 | TGTGTCTTTTATGAG[A/T]CATTCTGGCATTTTG | 9100 |
| rs776523129 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84716990 | TCATAGTAGAGCTTC[A/G]GGATTACATGAGATA | 9100 |
| rs776548893 | snp | C/T | 1.66324e-05 | 0.00288374 | intron-variant | USP10 | GRCh38.p7 | 16:84740275 | GTTTTAACATTTTGT[C/T]GAATTAAAATTTGTT | 9100 |
| rs776552578 | snp | C/T | 1.66065e-05 | 0.00288149 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744826 | TGGCTCCATCGACTG[C/T]CAGTACCCAGGCTCT | 9100 |
| rs776559739 | snp | C/T | | | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84760267 | AACAAGTCAAGCCTG[C/T]CTGAAAAGGTTTGAG | 9100 |
| rs776584919 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84752620 | TGGTATTAGTTCTGG[A/C]TTGTCCGTAAGACCT | 9100 |
| rs776595904 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84748006 | AAAAAACCTAAAAAT[C/T]AGCCAGGCGTGGTGG | 9100 |
| rs776599796 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84710859 | GCTCAGGTTGCAGGT[C/T]GTCCGCATGGGTTTG | 9100 |
| rs776634073 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84736609 | ATTTATGTTCAGAAA[C/G]AAAGAGAAAATGCTC | 9100 |
| rs776677299 | snp | A/G | 3.31708e-05 | 0.00407238 | intron-variant | USP10 | GRCh38.p7 | 16:84775144 | TGCTTCAAGCCATTG[A/G]TATTTTGTTTTCCAG | 9100 |
| rs776681804 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84754394 | TTATTCTGCGTTTAA[C/T]GACGTCGTACCAGAA | 9100 |
| rs776755874 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84735829 | AGTTTATCAAAATCA[C/T]AGTAACCTGCAAAAG | 9100 |
| rs776823223 | snp | A/G | 1.69861e-05 | 0.00291424 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745310 | CCCTGCGTTGGTACC[A/G]ATACTACTGAAAACC | 9100 |
| rs776835969 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84714020 | GCCTGAAAAGTTCTG[A/G]GAGACTAGAAAGGCT | 9100 |
| rs776836845 | snp | A/T | 1.65701e-05 | 0.00287833 | intron-variant | USP10 | GRCh38.p7 | 16:84740377 | ACCTGATGGTAAGCT[A/T]GTTCTCTCCTTATTT | 9100 |
| rs776907182 | in-del | -/A | | | intron-variant | USP10 | GRCh38.p7 | 16:84762248 | TCCATCATCAAAGAC[-/A]AGACAGAAGCAGACA | 9100 |
| rs776924439 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84775238 | CAGGTGAGTAAATTT[A/G]TACGACATTACTTCT | 9100 |
| rs776931414 | snp | C/G | 1.66263e-05 | 0.00288321 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744986 | AAAGATGGTGGCGAT[C/G]ATAGTATCTCCACAG | 9100 |
| rs776940732 | in-del | -/TT | | | intron-variant | USP10 | GRCh38.p7 | 16:84730977 | TATAGCATTTCTACC[-/TT]TTTTTTTTTTTTTTT | 9100 |
| rs776947086 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84755087 | AGTGGAGTTAGCCTC[A/G]TCATAAAGCGTGTTT | 9100 |
| rs776994641 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84778752 | AAATAGCATTGGTTT[G/T]TGTGATGACATCTCT | 9100 |
| rs777010626 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84705078 | CGGTTGTCATTCTTC[A/G]GATCCATTCTCAGTT | 9100 |
| rs777036707 | snp | C/G | 1.67052e-05 | 0.00289004 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744921 | GTGGTCTTGGACAAA[C/G]GGAGCGTAAAAAGAA | 9100 |
| rs777046684 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84714161 | GACCCAGTTGAGAAG[C/T]GTGGAGGGCTTGAAC | 9100 |
| rs777053712 | snp | C/T | 5.02306e-05 | 0.00501127 | intron-variant | USP10 | GRCh38.p7 | 16:84762983 | GATTATATTTGACCT[C/T]TTCAGGGTCGACAAG | 9100 |
| rs777076547 | in-del | -/GTG | 0.000187919 | 0.00969144 | intron-variant | USP10 | GRCh38.p7 | 16:84759314 | GTGCCTTCAGGAAAT[-/GTG]GTGTGTCTGTTCATT | 9100 |
| rs777087743 | in-del | -/ACTGCCCTT | | | intron-variant | USP10 | GRCh38.p7 | 16:84738499 | ATGGCCGCTGTGTCC[-/ACTGCCCTT]ATAGACCCACCTCTC | 9100 |
| rs777104630 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84704315 | GTAGTGGGAAGAGCT[C/T]GCTTTTGAATTTGTA | 9100 |
| rs777109418 | snp | A/G/T | 3.41666e-05 | 0.00413308 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745158 | ACATTGTGCCTGACA[A/G/T]TCCTTTCCCCGGAGC | 9100 |
| rs777128531 | snp | A/C | 1.73742e-05 | 0.00294734 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779113 | TGTGTGCGCCCAGTG[A/C]CCGCTTCGTAGGACA | 9100 |
| rs777136687 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84724910 | AGTTGAAAGCACACA[A/G]TGATTGTTCAGTAGA | 9100 |
| rs777148356 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84735693 | TTATTCACAGAAGAC[A/G]TGACTGTGTCTCATG | 9100 |
| rs777155822 | snp | A/T | 3.32281e-05 | 0.0040759 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84763084 | TCTCTCACCAAGTAA[A/T]GAAAGTAGGTTATGG | 9100 |
| rs777174027 | in-del | -/T/TT | 0.294476 | 0.258515 | intron-variant | USP10 | GRCh38.p7 | 16:84732444 | GACTTCTTCTTCTTC[-/T/TT]TTTTTTTTTTTTTTC | 9100 |
| rs777174987 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84717066 | CTGCGGGTCTTGTGA[A/G]TGTGCACATTTAGAT | 9100 |
| rs777192750 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84703034 | AAACTCCATCTCAAA[A/G]TAAATAAAAAAGTTT | 9100 |
| rs777196186 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84761735 | AAAGCACATTGCTTG[C/T]GCAAACGGTTTAGGC | 9100 |
| rs777204795 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84760834 | GCCGCCCTTAGCACC[A/G]TTAACTGGAGCATTT | 9100 |
| rs777207737 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84769824 | AGTTTGACTTTGCTG[C/G]GGTGGGCTGGTAGGG | 9100 |
| rs777225018 | in-del | -/A | | | intron-variant | USP10 | GRCh38.p7 | 16:84768513 | TATGGTTTTACAATG[-/A]AAATGGTTGAAACGT | 9100 |
| rs777247670 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84724520 | CTGTGAGAGTGACTT[C/T]GTGATAGTTTGTCTA | 9100 |
| rs777276018 | in-del | -/AA/AAA | | | intron-variant | USP10 | GRCh38.p7 | 16:84750404 | GAGTGAGACTGTCTC[-/AA/AAA]AAAAAAAAAAAAAAA | 9100 |
| rs777294363 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718499 | GCGGTGGCTCACGCC[-/TG]TGTAATCCCAGCACT | 9100 |
| rs777299147 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84776655 | CCCTGGAGGCTCTTG[C/T]GGGGGACATCACTGG | 9100 |
| rs777317712 | in-del | -/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84727874 | TACATTGATGCAGTA[-/C]TTTTTTCTAACCTGT | 9100 |
| rs777318812 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84716711 | CAGAGTTACTGGGAT[A/C]TTAGGTGCACGACCT | 9100 |
| rs777332485 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84725650 | CTCAGGTGATCCACC[C/T]GCCTCGGCCCCCCAG | 9100 |
| rs777337753 | in-del | -/ATAAC | | | intron-variant | USP10 | GRCh38.p7 | 16:84742830 | TGTTTGATACTAATT[-/ATAAC]ATACTGAAATGGTTC | 9100 |
| rs777338671 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717277 | CTAATTCCCTTACAT[C/G]AGTTTCTCGGGAGGT | 9100 |
| rs777346319 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84727910 | TTCTAATTTTGGGAG[C/T]TGACCATATAATGTC | 9100 |
| rs777404021 | snp | C/T | 1.69075e-05 | 0.00290748 | intron-variant | USP10 | GRCh38.p7 | 16:84762945 | CCTGCAGGCCTTTGA[C/T]AGTGATCAGTTCACA | 9100 |
| rs777458046 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84762289 | TAGCTCATTGCTCGA[C/G]TGGTGACCCTTGCAG | 9100 |
| rs777468768 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84703502 | TATGGCTGAATGTTA[C/G]TGTATTGCTGAATAT | 9100 |
| rs777499735 | snp | C/T | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699798 | TCCACAGCCAGGCCT[C/T]GGCGGGCTCCTGGTG | 9100 |
| rs777501034 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84730384 | TCCCCTAGTTAATTC[G/T]GTAATTTGATTGAAG | 9100 |
| rs777517196 | snp | A/G | 1.74952e-05 | 0.00295758 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745524 | CCAGCCTCTTTCATG[A/G]TTCTAAGCCCTCTTC | 9100 |
| rs777536524 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84736285 | TTTCTCTACTTGGGG[C/T]CATGAATTGAAAAAC | 9100 |
| rs777536548 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84743068 | TCTGGGGAGCCTTGA[C/T]GGCCCCAGAACATCA | 9100 |
| rs777544543 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84716847 | GTCTAAACTTATCCC[A/G]GCATAATTCATCATA | 9100 |
| rs777554025 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84731128 | GGGACTACAGGTGCA[C/T]GCCACCATGCCCGGC | 9100 |
| rs777556188 | in-del | -/A | 3.19371e-05 | 0.00399594 | intron-variant | USP10 | GRCh38.p7 | 16:84744584 | TAATTACTGGTACTT[-/A]AGAGTTTGTAGAACT | 9100 |
| rs777571762 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84774013 | CCAGCACTTTGGGAG[G/T]CCGAGGCAGGCAGAT | 9100 |
| rs777604289 | in-del | -/TGTG | | | intron-variant | USP10 | GRCh38.p7 | 16:84765256 | CATCACAGTTACCCT[-/TGTG]TGTGTGTGTGTGCAC | 9100 |
| rs777615323 | in-del | -/CTT | | | intron-variant | USP10 | GRCh38.p7 | 16:84732434 | TCTTCTCAATGACTT[-/CTT]CTTCTTCTTCTTTTT | 9100 |
| rs777648163 | in-del | -/A | 1.65905e-05 | 0.0028801 | frameshift-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764145 | AAGAGCAGGAAGAAC[-/A]AAGGTGAAGGAAGCG | 9100 |
| rs777686136 | in-del | -/A | | | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719758 | CATATCCAGGAACTT[-/A]AATACATAATTAAAG | 9100 |
| rs777702028 | snp | C/G | 1.65605e-05 | 0.0028775 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84772589 | CTCCCTCCTGTCCTC[C/G]TGCTGCACCTGAAAC | 9100 |
| rs777743168 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84776429 | CTCTTCTTTTCTCCC[C/T]CCGATCACAATTCCT | 9100 |
| rs777764804 | snp | A/G | 0.000185753 | 0.00963545 | utr-variant-5-prime, intron-variant | USP10 | GRCh38.p7 | 16:84704802 | AGCTCTACCAGCACT[A/G]CCATTCTGTCCCGTC | 9100 |
| rs777765397 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84756777 | ATGCACCTTTTTAAC[A/G]CTGCAATGACATTAG | 9100 |
| rs777778676 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84721783 | GCTCACTGCAACCTC[C/T]GCCTCCCGGGTTCAA | 9100 |
| rs777792061 | snp | A/G | 2.62698e-05 | 0.00362412 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84760249 | TACAGACTCCTGACA[A/G]TTAACAAGTCAAGCC | 9100 |
| rs777796040 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84768934 | GCTTGGTGGAGTCCT[C/T]GTCAACTCAGTTGGG | 9100 |
| rs777819837 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84714670 | TTTTTTGGTCCAATT[G/T]TTAGTTGTTACTTGT | 9100 |
| rs777837604 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84749072 | TTGTTGACAGTTTCA[A/G]GAGTCTCGTGAGATA | 9100 |
| rs777839662 | snp | C/T | 6.64408e-05 | 0.00576333 | intron-variant | USP10 | GRCh38.p7 | 16:84733532 | TTGTTTTAGTGAGTC[C/T]GTGGGTAGATACAAT | 9100 |
| rs777855356 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84759069 | AATAGTCACAAATAA[C/T]AGGGCAGAGCAACCA | 9100 |
| rs777865769 | snp | C/G | 0.000142136 | 0.00842899 | utr-variant-5-prime, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84700047 | GGCGGGGGAAGCAGC[C/G]TGAGCAGCCGGAGGA | 9100 |
| rs777887378 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84772302 | GTGATCCGCCTGTCT[C/T]AGCCTCCCAAAGTGC | 9100 |
| rs777894157 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84751622 | GGTAGTGGTACATTT[A/T]GGTCACTTTGCTGTC | 9100 |
| rs777894633 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84741455 | CACGTGGTGAGCATG[A/C]TGCTCATGTTGAACC | 9100 |
| rs777946635 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84706205 | TCATTCTGCAAGTAT[C/G]AGTCTTTTTACTTTT | 9100 |
| rs777947257 | snp | C/G | 3.31345e-05 | 0.00407016 | missense, intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84740364 | CTGTGGATAAACTAC[C/G]TGATGGTAAGCTAGT | 9100 |
| rs777963852 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84712804 | TCCAGGTGACTGACC[C/T]GCACGTCACATATAA | 9100 |
| rs777971533 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84704169 | TTCGGTTTTTTGTTT[A/G]TTTGTTTGTTTTTAA | 9100 |
| rs777980492 | snp | G/T | 1.67787e-05 | 0.00289639 | intron-variant | USP10 | GRCh38.p7 | 16:84764287 | TTTTCTGGAATAACT[G/T]AATATTTGCCTTTTC | 9100 |
| rs778009553 | snp | A/G | 1.66007e-05 | 0.00288098 | intron-variant | USP10 | GRCh38.p7 | 16:84733512 | AGTTGAGGTAAGACA[A/G]AACTTTGTTTTAGTG | 9100 |
| rs778047770 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84753906 | CAGAAAGGAACAGAT[A/G]GCAGCTGTTTGTAGG | 9100 |
| rs778082412 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84720428 | TGTCTTTGTGTGGAG[G/T]TTGAGTACATGGTCC | 9100 |
| rs778124472 | snp | A/T | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717784 | TACTGCCTTTGATTC[A/T]TTGAGGTCCTAGTCT | 9100 |
| rs778160603 | snp | A/G | 3.41752e-05 | 0.00413357 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745301 | GGGGCTCAGCCCTGC[A/G]TTGGTACCGATACTA | 9100 |
| rs778162907 | snp | C/T | 6.69972e-05 | 0.00578741 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745359 | AAATACTTGAATCCT[C/T]GGGTGAGGGCACAGC | 9100 |
| rs778176458 | snp | C/T | 2.57662e-05 | 0.00358921 | intron-variant | USP10 | GRCh38.p7 | 16:84778847 | AGACCTGTAATGATT[C/T]GTGTGCAGTGCTGTT | 9100 |
| rs778188702 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84713836 | TATAGTTTGCAGAGT[C/T]AGCCAGGCCAGCAGG | 9100 |
| rs778189011 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84740030 | ATTTCATTGTAGCTG[A/G]TTTACATGTCCATTG | 9100 |
| rs778190550 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84721886 | GTGTTTTCATAGAGA[C/T]AGGGTTTCACCGTGT | 9100 |
| rs778236799 | snp | A/T | 3.68976e-05 | 0.00429505 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744634 | TTCTTTCTAAACAGG[A/T]CAAGAATATCAGAGA | 9100 |
| rs778242461 | snp | C/T | 3.3157e-05 | 0.00407154 | intron-variant | USP10 | GRCh38.p7 | 16:84758705 | TGAAATATGCTTCTT[C/T]ACTCTTTCAGAGTTG | 9100 |
| rs778254560 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84731083 | CTCCCGGGTTCAAGC[A/G]ATTCTCCTGCATCAG | 9100 |
| rs778278034 | snp | A/G | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699539 | GGGAGTGAATGAAGA[A/G]TGAACAAATGAATGA | 9100 |
| rs778311642 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84723584 | CTTTTTATTTGTGTG[G/T]GTTTTTTCATCTTCC | 9100 |
| rs778315730 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84774721 | GTGATCGCCCGTCTC[A/T]GCCTCCCAAAGTGCT | 9100 |
| rs778331061 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84700820 | TGGGGGCCCTTTACA[A/G]TAATCCCGTGGTGGA | 9100 |
| rs778336667 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84739595 | AAACTTTCTTACACC[C/T]AATGTGTCCATTGGA | 9100 |
| rs778344353 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84775944 | GTTTGCCGCACTTTT[C/G]TTTGCTTCCCAGGCT | 9100 |
| rs778441616 | snp | C/T | 1.65682e-05 | 0.00287817 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84759937 | CCAGTACCTCCAAAA[C/T]CCCGACAAGGTTAGT | 9100 |
| rs778442411 | snp | A/T | 2.73804e-05 | 0.00369992 | intron-variant | USP10 | GRCh38.p7 | 16:84764048 | TTTTTGCTGTTCTTG[A/T]CGTAAATAGTAGTGT | 9100 |
| rs778443836 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84766644 | CAGCATACTCAAAGA[C/T]CCCAAATTTGTCTAA | 9100 |
| rs778452227 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84767749 | GTTAGAAATACTAAG[A/G]AGGTGCTATTCAGCA | 9100 |
| rs778457308 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84722778 | TTGGCCAGTCTCGAA[C/G]TCCCTAACCTCAAGT | 9100 |
| rs778538822 | snp | C/G | 1.65605e-05 | 0.0028775 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84772580 | CTGGAAAAACTCCCT[C/G]CTGTCCTCGTGCTGC | 9100 |
| rs778611240 | snp | A/G | 1.66927e-05 | 0.00288895 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745073 | GATGCAGAATTTATG[A/G]GTGACATGCCCCCGT | 9100 |
| rs778639246 | snp | A/G | 7.02469e-05 | 0.00592609 | intron-variant | USP10 | GRCh38.p7 | 16:84745688 | GGTATAGTTGAAAAG[A/G]TACAAATCTAGAGTG | 9100 |
| rs778644497 | snp | C/T | 0.000409109 | 0.0142964 | intron-variant | USP10 | GRCh38.p7 | 16:84760162 | AACCTGTGTCCTCTT[C/T]CCATTGCAGCTCTTG | 9100 |
| rs778645908 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84707894 | GACCAGCCTGGGCAA[C/T]GTAGCAAAACTCTTT | 9100 |
| rs778683322 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84737471 | GTGCATCTGATGTGT[A/G]AGGGAGGTTTGCTGA | 9100 |
| rs778752674 | snp | A/C | 5.0197e-05 | 0.00500959 | | | GRCh38.p7 | 16:84768339 | CTGTCCAAGGTTATA[A/C]CACAAAAACCAAACA | 9100 |
| rs778780666 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84767517 | CATTAAAAATCCTCT[A/G]TTTACCTTGGGATTT | 9100 |
| rs778807255 | snp | A/G | 1.66299e-05 | 0.00288352 | missense, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84733438 | ATTTTTTTTCAGTAT[A/G]TTTTTGGAGATTTTA | 9100 |
| rs778822337 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84775419 | ATTATCATCTTGGCC[C/T]TGAGGACAGATAACA | 9100 |
| rs778855922 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84712189 | CAGGCTTTGAGGGCC[C/G]TTATACTTTGATTCT | 9100 |
| rs778894157 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84704279 | GACACTTATTACTGG[C/T]ACTATACCAAAATAT | 9100 |
| rs778903127 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84763744 | CAGTGGATCCAGTGG[C/T]ATTGCGCCTGTTGTG | 9100 |
| rs778993043 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84765868 | AAGTCCTTCGGAAAG[A/G]TTTTTCTTTATTTAC | 9100 |
| rs779001911 | snp | A/G | 1.70304e-05 | 0.00291803 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745154 | AGTGACATTGTGCCT[A/G]ACAGTCCTTTCCCCG | 9100 |
| rs779003854 | snp | A/G | 3.35497e-05 | 0.00409558 | intron-variant | USP10 | GRCh38.p7 | 16:84733387 | TTTTTCTGAAAGTAT[A/G]TAATTTGTATATTTT | 9100 |
| rs779038440 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84755725 | ATTGCTTGAGACCCA[G/T]AGGCGGAGGTTGGAG | 9100 |
| rs779045059 | in-del | -/AC | | | intron-variant | USP10 | GRCh38.p7 | 16:84766387 | AAACACCCAGCCCTG[-/AC]CACTGTCTGTGGTTC | 9100 |
| rs779064738 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84732216 | TTCATTTATGTAATA[A/T]TTAGTTACTGGTTAT | 9100 |
| rs779102187 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84758110 | AGCAGCGTGTTTGTA[A/G]ATGGAATAAGGGAAT | 9100 |
| rs779108364 | snp | C/T | 1.72267e-05 | 0.0029348 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745498 | TCCTGTCAGCCAGCC[C/T]AAGTCCTGGGCCAGC | 9100 |
| rs779136064 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84772165 | CAAGGGATTCTCTTG[A/C]CTCTGCCACCCAGGT | 9100 |
| rs779136449 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84739993 | CACTGACATCCTGTG[C/G]AAAGAAGGATGTATC | 9100 |
| rs779143143 | snp | A/G | | | utr-variant-5-prime, intron-variant | USP10 | GRCh38.p7 | 16:84704825 | GTCCCGTCTTGAAAC[A/G]TCATGCCCTGGTTGC | 9100 |
| rs779151385 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84777200 | GGGGGGCTTGCAGGT[A/G]TGAGTGACACACGGC | 9100 |
| rs779169908 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84721379 | TAAATGAAAGATTAC[A/G]ACTGTGGCCATTGGT | 9100 |
| rs779206848 | snp | A/C/G | 3.48167e-05 | 0.00417221 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745221 | CAGAGGGGGGCCCCG[A/C/G]GGCTGATTTTGGTCA | 9100 |
| rs779219140 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84727130 | GCTCTGCACTTTCTT[C/T]GAAATTACAAGAAAC | 9100 |
| rs779240079 | snp | C/T | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84699302 | AGGCAGGGGCCCCTG[C/T]TTCTTAATAATGAAT | 9100 |
| rs779261997 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84724720 | AAATGTCACCATGCC[C/G]TGACCCCTGTGTGTG | 9100 |
| rs779267974 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84752487 | CATTTTTATTCTTTT[A/G]GCCTCCATAATTGGA | 9100 |
| rs779296259 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84735604 | CAGCTAATGTATGGT[C/G]CGATAACTAGTGAGT | 9100 |
| rs779296840 | snp | C/T | 1.71557e-05 | 0.00292875 | synonymous-codon, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745291 | AAGGACAGCTGGGGC[C/T]CAGCCCTGCGTTGGT | 9100 |
| rs779297574 | snp | C/T | 1.65679e-05 | 0.00287814 | synonymous-codon, nc-transcript-variant, intron-variant | USP10 | GRCh38.p7 | 16:84759420 | ATGAAGTTCATTCCT[C/T]TGTATTCCAAAGTGC | 9100 |
| rs779306261 | snp | A/G | 0.000117945 | 0.00767846 | missense, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84778945 | CATTACACTACAGAC[A/G]TCTTCCAGATCGGTC | 9100 |
| rs779334767 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84732599 | CTACAGGTACACGCC[A/C]CCACGCCTGGCTAAT | 9100 |
| rs779367707 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84728192 | GCAGTTGGCTGTCCT[A/G]AATTTCTGTGATAAA | 9100 |
| rs779376353 | snp | A/G | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698090 | ATATCGCTTTTCCAT[A/G]GTTAAAATTATAGCA | 9100 |
| rs779408269 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84708295 | TCTCTGCTAAAAATA[C/G]AAAAATTAGCCGAGT | 9100 |
| rs779441687 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84752429 | CAGGTCAAGTTTCAA[C/G]CTAGAAGTTGCCTGC | 9100 |
| rs779464018 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84720289 | GGCCTTCTGTTGGTC[C/T]GGTTCCAGCGTATTT | 9100 |
| rs779490702 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84730543 | AAAACTCAGTGAACC[A/G]TTTCTGAGCGTTCCA | 9100 |
| rs779495853 | in-del | A/GTGTGTGTGTGTGTGTGTGTGTGTG | | | intron-variant | USP10 | GRCh38.p7 | 16:84735197 | TGCCAGGCCCGGGTG[A/GTGTGTGTGTGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 9100 |
| rs779501993 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84774608 | CCCGAGTAGCTGAGA[C/T]TACAGCCGCGTGCCA | 9100 |
| rs779527442 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84711250 | TTGCAAAAAAACATG[C/T]TTTTAAAAATGTAAG | 9100 |
| rs779544573 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84712690 | TTCCCACAGTATCAC[A/C]TTGATTGTCATTTCT | 9100 |
| rs779560918 | snp | C/G | 1.69611e-05 | 0.00291209 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745132 | CCAGAACTCCACAGA[C/G]TCTGTCAGTGACATT | 9100 |
| rs779564834 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84710374 | TTAGGCTCTCCTCCA[C/T]AGCTGGGACTCTACT | 9100 |
| rs779569587 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84748432 | CCTCAGCCTCCCTAG[C/T]AGCTGGGACTACAGG | 9100 |
| rs779592460 | snp | A/G | 4.96964e-05 | 0.00498455 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84775205 | ATTTTAAATGCCACC[A/G]AACCTATCGGCTCTT | 9100 |
| rs779616001 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84738557 | CATCAATGCTGGTGT[A/G]TGGAATGGTCTTTGC | 9100 |
| rs779662350 | snp | C/T | 1.66746e-05 | 0.00288739 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84745060 | TGTCAGTGCAGAGGA[C/T]GCAGAATTTATGGGT | 9100 |
| rs779671297 | snp | G/T | 1.65658e-05 | 0.00287795 | missense, intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84740356 | CACACAGGCTGTGGA[G/T]AAACTACCTGATGGT | 9100 |
| rs779675788 | snp | G/T | 1.65831e-05 | 0.00287945 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84763066 | GTTGAACCTAAAGAA[G/T]CTTCTCTCACCAAGT | 9100 |
| rs779682773 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84725545 | AGCTGAGATTAGAGG[C/T]GCCTGCCACCATGCC | 9100 |
| rs779687376 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84731937 | TATTCTTCACTGAAA[A/G]GTGACAGTATTTCAG | 9100 |
| rs779716940 | in-del | -/ATTA | | | intron-variant | USP10 | GRCh38.p7 | 16:84714932 | ATTATTATTATTATT[-/ATTA]TTTTTTTTTTTTGAG | 9100 |
| rs779717777 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84736398 | TTGTCTTTTAGTTTG[C/T]TTGCTTGGCAGCTTG | 9100 |
| rs779731072 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84722204 | AGAATTACACAAACT[A/G]TACTCTTTTGTTTGG | 9100 |
| rs779732194 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84740646 | TGAGTGCAACAGGTA[C/T]GTTACTCTTCATCAG | 9100 |
| rs779733147 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84730011 | TTTGAAGAGTTGTAA[G/T]GTGATTTCTGTTGTG | 9100 |
| rs779764742 | snp | C/T | 0.000916842 | 0.0213911 | intron-variant | USP10 | GRCh38.p7 | 16:84733116 | GAAAGGTAAATGGAA[C/T]AACTGGCAGTATTTG | 9100 |
| rs779767499 | snp | A/T | 2.98458e-05 | 0.0038629 | intron-variant | USP10 | GRCh38.p7 | 16:84745677 | TAAAGATTGCAGGTA[A/T]AGTTGAAAAGATACA | 9100 |
| rs779778682 | snp | A/G | 1.65688e-05 | 0.00287821 | intron-variant | USP10 | GRCh38.p7 | 16:84759957 | ACAAGGTTAGTAAAA[A/G]TGAGTTTTGTTGATG | 9100 |
| rs779779251 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84750971 | AGTTATTACAATTTG[C/G]GTCTTCTCTAATGAA | 9100 |
| rs779785993 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84722717 | GGCAGACTCCCCCAC[A/G]CCCAGCTAATTTTTG | 9100 |
| rs779788797 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84767503 | TAGGAGGAAAATGCC[A/G]TTAAAAATCCTCTAT | 9100 |
| rs779799767 | snp | A/G | 1.65477e-05 | 0.00287638 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84768311 | GCACTGGAGAGCTTG[A/G]TGGCAAGAGAATCTG | 9100 |
| rs779808881 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84748840 | AGTAAGGGCCTCTTA[A/G]TGACTGGTAGTAGAG | 9100 |
| rs779860050 | snp | G/T | 0.000326851 | 0.0127796 | intron-variant | USP10 | GRCh38.p7 | 16:84732433 | ATTCTTCTCAATGAC[G/T]TCTTCTTCTTCTTTT | 9100 |
| rs779887926 | snp | C/T | 0.000116153 | 0.0076199 | intron-variant | USP10 | GRCh38.p7 | 16:84772491 | GGATGTGGTGTTAGC[C/T]GTTGCAAGTAAGACA | 9100 |
| rs779892259 | in-del | -/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84774710 | TCCTGACCTCGTGAT[-/C]CGCCCGTCTCAGCCT | 9100 |
| rs779902018 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84710612 | CCCTTGATTATATTC[A/G]TAGAAAATATTAAGG | 9100 |
| rs779927793 | in-del | -/TGCCCCTC | | | intron-variant | USP10 | GRCh38.p7 | 16:84777955 | GGCCAGGCAGACCTG[-/TGCCCCTC]TGCTCCATAGAAGTG | 9100 |
| rs779974997 | snp | A/G | | | intron-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84719268 | TTTTAACTGGGAGGC[A/G]TAACTGAATGGAGAA | 9100 |
| rs779976790 | snp | A/C | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718443 | TTTTTCTGTCATATT[A/C]CTTCTAATTTAGTTG | 9100 |
| rs779994043 | snp | C/T | 1.853e-05 | 0.00304379 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779132 | CTTCGTAGGACACCA[C/T]CTCACACTCACTTCC | 9100 |
| rs780056292 | snp | A/G/T | 3.32786e-05 | 0.00407902 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744975 | ACAGCTATTTGAAAG[A/G/T]TGGTGGCGATGATAG | 9100 |
| rs780062569 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84754142 | CACTAATATCAGGTA[A/G]GCAGTGATGAGGTCA | 9100 |
| rs780107451 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84762106 | AATCAAACACTCGTG[A/C]TGTGGGATTATTAAA | 9100 |
| rs780107924 | snp | C/G | | | upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84698072 | GTTTCTATCCAAGTG[C/G]AGATATCGCTTTTCC | 9100 |
| rs780126575 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84772085 | GAGACAAGATCTCGC[C/T]GTGTTGCCCAGGCTG | 9100 |
| rs780152021 | snp | A/G | 5.01006e-05 | 0.00500478 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745376 | GGTGAGGGCACAGCT[A/G]CCAACGGGGTGGAGT | 9100 |
| rs780154296 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84702656 | ACTTGTTAAAGTTAA[A/T]TTTGTCACTGAGAAT | 9100 |
| rs780161426 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84727665 | ACACTCATACGGATA[C/G]ACATACAGACACACA | 9100 |
| rs780167167 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84764067 | AAATAGTAGTGTAAG[A/C]AGATGCTCTCCTTTT | 9100 |
| rs780190266 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84738491 | AGACACACATGGCCG[C/G]TGTGTCCACTGCCCT | 9100 |
| rs780199793 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84739429 | GGTGCCTGCCACCAC[A/G]CCCAGCTGATTTTTT | 9100 |
| rs780199981 | in-del | -/AA | 2.61619e-05 | 0.00361667 | frameshift-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84768354 | CCACAAAAACCAAAC[-/AA]GAGGTATGTTCACAC | 9100 |
| rs780210390 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84737023 | TTGATCTCCTGACCT[C/T]GTGGTCTGCCCGCCT | 9100 |
| rs780214525 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84720247 | TGGCGATGTGCGTTC[C/T]TTCCTGGCGGGTGGC | 9100 |
| rs780218036 | in-del | -/AAGTCA | 1.87513e-05 | 0.00306191 | cds-indel, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745617 | CTGAAAAGCAGGTTG[-/AAGTCA]AAGAAGGGCTTGTTC | 9100 |
| rs780219874 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84764786 | CAGTGGCCCAGATAG[C/T]GCCATTGCACTCCAG | 9100 |
| rs780259084 | in-del | -/AAATG | | | intron-variant | USP10 | GRCh38.p7 | 16:84740135 | TGTGTTTTTTTCGTT[-/AAATG]AAGATGATTTAGATT | 9100 |
| rs780302913 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84737608 | AGTAAGTGTGTTGAG[C/T]ATGCTTACTGAAGGT | 9100 |
| rs780311762 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84712629 | GAGGGGCAGATTTGC[C/T]GTCTATAGAAATAGT | 9100 |
| rs780335385 | snp | C/G | 3.59305e-05 | 0.00423839 | intron-variant | USP10 | GRCh38.p7 | 16:84760150 | TGTAGTTAGGAAAAC[C/G]TGTGTCCTCTTTCCA | 9100 |
| rs780360388 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84733887 | GCTTTAAAGTGTCAC[A/G]TAAATGGTATACTAT | 9100 |
| rs780361588 | snp | C/T | 1.69608e-05 | 0.00291206 | missense, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84778937 | CGGGCGGCCATTACA[C/T]TACAGACGTCTTCCA | 9100 |
| rs780366765 | snp | A/T | 1.6582e-05 | 0.00287936 | intron-variant | USP10 | GRCh38.p7 | 16:84758833 | TGGACGCCGTCCGCA[A/T]GGCCAGCTTGTTGCA | 9100 |
| rs780369832 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84708175 | AGAGGTCTGGCTGGG[C/T]GTGGTGGCTCACGCG | 9100 |
| rs780411457 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84734698 | TAGTTTTAAAAATAT[C/G]TTTAGGAAATTCTTC | 9100 |
| rs780418742 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84760649 | TGGAATGATGGCAGT[A/G]TTCAGAAGAGCTTAT | 9100 |
| rs780433322 | snp | A/G | 1.65795e-05 | 0.00287914 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764202 | CGGAACAAGACTTCC[A/G]TCACCCGCCAGGCGG | 9100 |
| rs780451163 | snp | A/G | 1.66255e-05 | 0.00288314 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84764133 | TCGGTCAATGAAGAA[A/G]AGCAGGAAGAACAAG | 9100 |
| rs780451911 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84715790 | AGTTACAGTTTTGAG[A/G]ACGTGGCTTCTTTTC | 9100 |
| rs780494484 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84726880 | GCAACCACAGGACGC[A/G]GGAAAGGAGCGTTTG | 9100 |
| rs780505106 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84707746 | GTGCTGCCACAACTT[A/G]TAACATGTTGTCCAA | 9100 |
| rs780510716 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84762009 | CAGTTTACCTAGATG[A/C]TTCAAACAGAACAAT | 9100 |
| rs780664993 | snp | A/G | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84717491 | TTTAAACTGCTTTTT[A/G]ATGTCCTTTTTATGT | 9100 |
| rs780693961 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84751746 | AGAATGATGACAGAA[A/G]AGCAGGTCAACAACA | 9100 |
| rs780704982 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84754053 | TACCTTAGATGGTGC[A/G]GACTTTGTTGAGCAG | 9100 |
| rs780740128 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84709291 | GAAGTGACGTGTTTA[C/T]AGCATGAGACAGTGG | 9100 |
| rs780770445 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84721363 | AGGAATTATTCTTCT[C/G]TAAATGAAAGATTAC | 9100 |
| rs780771677 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84725471 | AATGGCACGATTTCC[A/G]CTCACTGCAACCTCT | 9100 |
| rs780792665 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84749678 | GGACTATTTCCCCTA[C/T]TGTTAAGTCTGCTTA | 9100 |
| rs780829115 | snp | A/C | 1.68707e-05 | 0.00290432 | intron-variant | USP10 | GRCh38.p7 | 16:84772722 | GAGTGTTCGTGGTGA[A/C]ACACTCCTGCACATC | 9100 |
| rs780863110 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84747320 | ATGTAGCAGCAAGCT[A/G]CCAAATGCACACCCT | 9100 |
| rs780865994 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84736909 | TTCTCCTGCCTCAGC[C/T]TCCCGAGTAGCTGGG | 9100 |
| rs780867616 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84728563 | CTCAATCTCCTGACC[C/T]CGTGATCCGCCTGCC | 9100 |
| rs780888996 | snp | C/T | 1.66504e-05 | 0.0028853 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744965 | CCTGGATATTACAGC[C/T]ATTTGAAAGATGGTG | 9100 |
| rs780891711 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84747122 | CGAAATGTTACGCCG[C/T]GCGTGACTGTACGTA | 9100 |
| rs780897917 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84757964 | ATCACCATTAGAAGA[C/T]TCATAGTGGGACAGG | 9100 |
| rs780904523 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84716112 | ACTGGGTGACTACTA[-/T]TCCCACAGGGTAGGA | 9100 |
| rs780916220 | snp | A/C | 1.66713e-05 | 0.0028871 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744880 | TAATGTGGAGGCGGA[A/C]GTTTTGGAAAATGAT | 9100 |
| rs780917105 | snp | C/G | 1.68823e-05 | 0.00290532 | intron-variant | USP10 | GRCh38.p7 | 16:84762954 | CTTTGACAGTGATCA[C/G]TTCACAGTAACGTGA | 9100 |
| rs780930768 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84723773 | CACCCATTTAAAGTG[C/T]ATATTTCCATGAATT | 9100 |
| rs780980904 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84700704 | CTCGAAATAAGTCGC[A/G]AGGACCGTACTTTCA | 9100 |
| rs780989918 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84724599 | TTTTGCTATAGCCCT[A/G]TTAGTGAGGGAACAA | 9100 |
| rs781004071 | snp | G/T | 4.39889e-05 | 0.00468962 | utr-variant-5-prime, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84700061 | CGTGAGCAGCCGGAG[G/T]ATCGCGGAGTCCCAA | 9100 |
| rs781017814 | in-del | -/TA | | | intron-variant | USP10 | GRCh38.p7 | 16:84763412 | TACACACACTGTGTA[-/TA]TATATATATATGTCT | 9100 |
| rs781027169 | snp | A/G | 1.65608e-05 | 0.00287752 | synonymous-codon, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84772600 | CCTCGTGCTGCACCT[A/G]AAACGATTCGTTTAT | 9100 |
| rs781038767 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84717096 | TTCAGTACACCTGGG[A/G]TGGGCCCTGTGCGCT | 9100 |
| rs781048244 | in-del | -/CT | 3.3365e-05 | 0.00408429 | intron-variant | USP10 | GRCh38.p7 | 16:84733416 | TTATGTGATCAGTGA[-/CT]CTCTTATTTTTTTTC | 9100 |
| rs781074775 | in-del | -/GTT | | | intron-variant | USP10 | GRCh38.p7 | 16:84770038 | TGCCTGAGCCCAACA[-/GTT]GGAGGCTGCAGTGAG | 9100 |
| rs781086443 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84736933 | AGCTGGGACTACAGG[C/T]GTCCGCCACCTCGCC | 9100 |
| rs781093018 | in-del | -/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84725292 | TGAATGGAAGAAACA[-/C]ATTTATGGCTCTTTG | 9100 |
| rs781105422 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84726255 | CCCAGCGTCTCCTGA[A/G]GCCGAAAGTGGCGTT | 9100 |
| rs781185960 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84750143 | CCCGGCACAGTGGCT[C/T]ACGCCTGTAATCCCA | 9100 |
| rs781202733 | snp | C/G | 0.000258737 | 0.0113711 | missense, intron-variant, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84745598 | GCCATATCTCCCCTG[C/G]TTTCTGAAAAGCAGG | 9100 |
| rs781205396 | in-del | -/AAA | | | intron-variant | USP10 | GRCh38.p7 | 16:84755796 | GAGTGAGACTGTCTC[-/AAA]AAAAAAAAAAAAAAT | 9100 |
| rs781205872 | snp | C/T | 1.68451e-05 | 0.00290211 | intron-variant | USP10 | GRCh38.p7 | 16:84764301 | TTAATATTTGCCTTT[C/T]CTAGGGTTTTGCCAT | 9100 |
| rs781211107 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84705810 | CTGCAGCCTCTACCT[C/T]CCAGATTCAAGCGAT | 9100 |
| rs781241192 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84742656 | CCAAGCGTGCAGGCC[A/G]TCCTGCACTTCGTCT | 9100 |
| rs781252823 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84770107 | GTGAAACCGTGTCTC[C/T]AAAACATAAGAAGAA | 9100 |
| rs781304740 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84763884 | CTGTTGCGATTGGTT[A/G]CCGTGGATCCAGTGA | 9100 |
| rs781313371 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84771323 | GTGGGAGACTGAGGC[C/G]AGCAGGTTGCTTAAG | 9100 |
| rs781316897 | snp | A/G/T | 1.66054e-05 | 0.00288139 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744825 | ATGGCTCCATCGACT[A/G/T]CCAGTACCCAGGCTC | 9100 |
| rs781358790 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84726818 | TGTACTTTGCTCCCC[C/T]GAATCGCAGGCATTT | 9100 |
| rs781411858 | snp | A/T | 1.82337e-05 | 0.00301936 | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779126 | TGCCCGCTTCGTAGG[A/T]CACCACCTCACACTC | 9100 |
| rs781440149 | snp | C/T | | | intron-variant, upstream-variant-2KB | USP10 | GRCh38.p7 | 16:84718613 | ATACAAAAATTAGCC[C/T]AGACATCGTGGCACA | 9100 |
| rs781457002 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84763404 | CTGATGCTATACACA[C/T]ACTGTGTATATATAT | 9100 |
| rs781471453 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84744026 | GAGTGCTCTGAAGTG[C/T]GCTTTTATATATAGG | 9100 |
| rs781486291 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84748345 | GTCTCACTCTGTCGC[C/G]CAGGCCGGAATGCAG | 9100 |
| rs781490554 | in-del | -/TAAAT | | | intron-variant | USP10 | GRCh38.p7 | 16:84774254 | TCTCAAAAAAATAAA[-/TAAAT]AACATAAATGGGGGA | 9100 |
| rs781492952 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84715762 | CTTCAAAGTTGGTTT[A/C]ATTCAGCCGTTTAGT | 9100 |
| rs781495466 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84711490 | TTAAGCCAATTTACC[A/G]TCGGGAATTCCTGCT | 9100 |
| rs781514856 | snp | G/T | 0.000358304 | 0.01338 | intron-variant | USP10 | GRCh38.p7 | 16:84764057 | TTCTTGTCGTAAATA[G/T]TAGTGTAAGCAGATG | 9100 |
| rs781520737 | in-del | -/CTC | | | intron-variant | USP10 | GRCh38.p7 | 16:84730667 | TTGTTTTCTCCTCCT[-/CTC]CTCCTCTGCTGCCAA | 9100 |
| rs781521149 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84767344 | TAGAAAAAGGAAAAA[A/G]AAAATGAAATGAAAA | 9100 |
| rs781562254 | snp | A/C/T | 0.000118373 | 0.00769245 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744657 | ATCAGAGAATTGAGT[A/C/T]TGGTGTCGATGAAGT | 9100 |
| rs781579765 | snp | C/G | 1.65806e-05 | 0.00287924 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | USP10 | GRCh38.p7 | 16:84744706 | TTTGCCGAGAACCCC[C/G]AGCTACAGTATTTCA | 9100 |
| rs781592338 | in-del | -/ATAA | | | intron-variant | USP10 | GRCh38.p7 | 16:84748760 | TTTAAATATAGTTTG[-/ATAA]ATAGTTTGTTATGTT | 9100 |
| rs781605024 | snp | C/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84733757 | CTTTGGACCTCTCTC[C/G]CATCTCTCCCCAGAA | 9100 |
| rs781621967 | snp | C/G/T | 3.31297e-05 | 0.00406989 | missense, nc-transcript-variant | USP10 | GRCh38.p7 | 16:84775223 | CCTATCGGCTCTTTG[C/G/T]AGGTGAGTAAATTTG | 9100 |
| rs781674201 | snp | A/C/G | 1.75779e-05 | 0.00296457 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84778920 | TCACGGCAACAGTGC[A/C/G]ACGGGCGGCCATTAC | 9100 |
| rs781688228 | snp | G/T | 2.52835e-05 | 0.00355543 | intron-variant | USP10 | GRCh38.p7 | 16:84778849 | ACCTGTAATGATTCG[G/T]GTGCAGTGCTGTTCT | 9100 |
| rs781730161 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84766720 | GCTCAGATTGAACAG[C/T]TCTGTCACAGCTGCT | 9100 |
| rs781745579 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB | USP10, LOC105371378 | GRCh38.p7 | 16:84779157 | ACTTCCCGCCTCTCT[C/T]TAGTGGCTCTTTAGA | 9100 |
| rs796070575 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84765032 | GTGAGCCAAGATTAC[A/G]CCACTGCACTCCAGC | 9100 |
| rs796112090 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84763335 | AAAAAAGCTGAAAGA[A/G]TCGTTTGATGAATAC | 9100 |
| rs796160235 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84764515 | TCAAGTTCAGCTGCT[C/T]ACTGCTAGGGAGTAA | 9100 |
| rs796206112 | in-del | -/GT | | | intron-variant | USP10 | GRCh38.p7 | 16:84723364 | ATACTTTAAAAATAA[-/GT]GTTATTTCTTGATTG | 9100 |
| rs796309128 | in-del | GGG/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84757400 | GAATGAGAGGGGTGG[GGG/T]TGTGTGTGTGTGTGT | 9100 |
| rs796309566 | snp | A/C | | | intron-variant | USP10 | GRCh38.p7 | 16:84724986 | TAGTAAAGAAATTAA[A/C]ATTTTTATTTTGATA | 9100 |
| rs796337896 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84707594 | GAACTTTATTGAGCA[A/T]ACCTTGTTTTCAAAA | 9100 |
| rs796339654 | snp | G/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84735213 | TGTGTGTGTGTGTGT[G/T]TGTGTGTGTGTGTGT | 9100 |
| rs796362893 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84723159 | GGGTTTTTTTTTTTT[-/T]GGCCTTTTTTCCCCC | 9100 |
| rs796417665 | in-del | -/AA | | | intron-variant | USP10 | GRCh38.p7 | 16:84771055 | GAGCGAGACTGTCTC[-/AA]AAAAAAAAAAAAAAG | 9100 |
| rs796436741 | in-del | GAA/TTTTTTTTTTTTGAG | | | intron-variant | USP10 | GRCh38.p7 | 16:84747569 | TTTTTTTTTTTTTTT[GAA/TTTTTTTTTTTTGAG]TGCAGTCTCACTCTG | 9100 |
| rs796438597 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84765973 | GAAAGTACTGAAGAG[A/G]CCTCATTGGAGCCTA | 9100 |
| rs796443484 | multinucleotide-polymorphism | AAA/GAG | | | intron-variant | USP10 | GRCh38.p7 | 16:84764933 | ACGAGAGAGAGAGAA[AAA/GAG]AAAATATATATATAT | 9100 |
| rs796460010 | in-del | -/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84774472 | TGAAGTTTTGTTTTG[-/T]TTTTTTTTTTGTTTG | 9100 |
| rs796505439 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84765390 | TGTTCGCCTGTGTGG[C/T]TGCCCTTGGTGTCCT | 9100 |
| rs796509341 | in-del | -/AT | | | intron-variant | USP10 | GRCh38.p7 | 16:84714932 | ATTATTATTATTATT[-/AT]TATTTTTTTTTTTTG | 9100 |
| rs796568828 | in-del | -/TC | | | intron-variant | USP10 | GRCh38.p7 | 16:84778124 | GTGTGTGTGTTTTGT[-/TC]TGTTAAAACATAGAA | 9100 |
| rs796589020 | in-del | -/A | | | intron-variant | USP10 | GRCh38.p7 | 16:84756651 | CTTAAGGTTAGGTTT[-/A]AAAAAAAAAAGTCAT | 9100 |
| rs796693078 | in-del | -/A | | | intron-variant | USP10 | GRCh38.p7 | 16:84730844 | AAAACCTTCCTAAAG[-/A]AAAATACCTGATAAT | 9100 |
| rs796749151 | snp | A/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84755883 | TATCTTTTACTAACA[A/T]CTCTAAAACTGAGCT | 9100 |
| rs796755961 | in-del | -/A | | | intron-variant | USP10 | GRCh38.p7 | 16:84754989 | TAGACTTTGTCCCAG[-/A]AAAAAAAAAAAAAGG | 9100 |
| rs796779590 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84710790 | ACCCTGGGTGCCACC[A/G]AGAGACACTGAGTAA | 9100 |
| rs796929232 | in-del | -/TA | | | intron-variant | USP10 | GRCh38.p7 | 16:84767789 | TTATTTTTTTTAATT[-/TA]TTTTTTTATTGATAA | 9100 |
| rs796992703 | snp | A/G | | | intron-variant | USP10 | GRCh38.p7 | 16:84708344 | AATCCCAGCTGCTCC[A/G]AAGGCTGAGGCAGGA | 9100 |
| rs797009861 | snp | C/T | | | intron-variant | USP10 | GRCh38.p7 | 16:84736165 | GTAACATAATTGCCG[C/T]TCAAACATGCAGTGT | 9100 |