SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs169289 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | USP43 | GRCh38.p7 | 17:9668524 | ATTTTTCTTCACCAG[G/T]GGAAAGCAGCTTAGT | 124739 |
rs175629 | snp | C/T | 0 | 0 | intron-variant, nc-transcript-variant | USP43, LOC107985011 | GRCh38.p7 | 17:9647579 | gaaatgttcattaTT[C/T]TATCACGACCCCTTT | 124739 |
rs188000 | snp | C/T | 0 | 0 | intron-variant | USP43 | GRCh38.p7 | 17:9670083 | ccactgcactccagc[C/T]tgggtgatagcataa | 124739 |
rs190657 | snp | A/C | 0 | 0 | intron-variant, nc-transcript-variant | USP43, LOC107985011 | GRCh38.p7 | 17:9647677 | TTCCATCCAGTTACC[A/C]CAGCAATGGGAGAGG | 124739 |
rs190658 | snp | A/C | 0 | 0 | intron-variant, upstream-variant-2KB | USP43, LOC107985011 | GRCh38.p7 | 17:9647819 | accatcctggctaac[A/C]cggtgaaaccccgtc | 124739 |
rs190659 | snp | A/C | 0 | 0 | intron-variant, upstream-variant-2KB | USP43, LOC107985011 | GRCh38.p7 | 17:9647847 | gtctttactaaaaat[A/C]caaaaaaaaaaaaaa | 124739 |
rs274899 | snp | C/T | 0.475235 | 0.108485 | utr-variant-3-prime, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643234 | TCTTCAACAGGACTG[C/T]GTGCAACGCCAAGGC | 124739 |
rs274906 | snp | C/G | 0.211819 | 0.247067 | intron-variant | USP43 | GRCh38.p7 | 17:9670716 | cactccctcggaagt[C/G]ctccccacccccgat | 124739 |
rs274907 | snp | A/C | 0.451234 | 0.14834 | intron-variant | USP43 | GRCh38.p7 | 17:9661544 | ATAGTGAGACCTTGT[A/C]TCCACAAAACTAAAA | 124739 |
rs274908 | snp | A/G | 0.106987 | 0.205054 | intron-variant | USP43 | GRCh38.p7 | 17:9677218 | gatttaatcacaggc[A/G]tcctgtgaagtagac | 124739 |
rs370436 | snp | C/G | 0.435263 | 0.167862 | intron-variant | USP43 | GRCh38.p7 | 17:9711011 | ACTTATGTTAGGATT[C/G]GTTTAGACCTGCTGA | 124739 |
rs377779 | snp | C/G | 0.302184 | 0.244493 | intron-variant | USP43 | GRCh38.p7 | 17:9703895 | TGAGCTTCACCTAAA[C/G]GAGGGAGTTGACACT | 124739 |
rs378719 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | USP43 | GRCh38.p7 | 17:9719832 | tgatccacctgcctc[A/G]gcctcccaaagtgct | 124739 |
rs378841 | snp | C/G | 0.465263 | 0.127129 | intron-variant | USP43 | GRCh38.p7 | 17:9711701 | CTCCGTAAGTGCTGG[C/G]ATTACAGGCGTGAGC | 124739 |
rs379223 | snp | C/T | 0.460702 | 0.134554 | intron-variant | USP43 | GRCh38.p7 | 17:9711825 | CCCTCTCCTTGTTGA[C/T]AGGTTTCTGCAGTTC | 124739 |
rs382475 | snp | A/G | 0.2462 | 0.249971 | intron-variant | USP43 | GRCh38.p7 | 17:9706774 | TCAGCCTCCTGAGTA[A/G]CTGGGACTACAGGCG | 124739 |
rs391227 | snp | A/C | 0.438246 | 0.16451 | intron-variant | USP43 | GRCh38.p7 | 17:9703468 | CATACCACCACCCCC[A/C]AAATCGGGCATTCTG | 124739 |
rs396175 | snp | C/T | 0.271972 | 0.249033 | intron-variant | USP43 | GRCh38.p7 | 17:9719083 | TGGAGCGCAATGGTG[C/T]GAGCTCAGCTTACTG | 124739 |
rs401367 | snp | A/G | 0.495963 | 0.0447464 | intron-variant | USP43 | GRCh38.p7 | 17:9714408 | gaatgaaggccgggc[A/G]cagtggctcacgcct | 124739 |
rs401945 | snp | A/T | 0.330482 | 0.236691 | intron-variant | USP43 | GRCh38.p7 | 17:9690411 | TTACCAAAATTTTTT[A/T]AAAAATCAACGGGGT | 124739 |
rs407454 | snp | C/T | 0.300169 | 0.244914 | intron-variant | USP43 | GRCh38.p7 | 17:9703013 | TGCGGTGCCAGCCTG[C/T]TCTTCCACAGCTGTC | 124739 |
rs408537 | snp | A/G | 0.34303 | 0.232046 | intron-variant | USP43 | GRCh38.p7 | 17:9714123 | gatctgacaggaggc[A/G]gagctcaggcggtaa | 124739 |
rs415432 | snp | A/G | 0.49306 | 0.0584955 | intron-variant | USP43 | GRCh38.p7 | 17:9662170 | CCTCACCTACCAAGG[A/G]ATAGGCCCATGACCC | 124739 |
rs422819 | snp | C/T | 0.460702 | 0.134554 | intron-variant | USP43 | GRCh38.p7 | 17:9652060 | CATGGCATAACTCTA[C/T]CTGTATGTATGTTTT | 124739 |
rs423020 | snp | C/T | 0 | 0 | intron-variant | USP43 | GRCh38.p7 | 17:9721065 | TTCCCCCACACCCAC[C/T]TCAATTATATAAGTT | 124739 |
rs427096 | snp | A/G | 0.493154 | 0.0581045 | intron-variant | USP43 | GRCh38.p7 | 17:9711673 | GAGGCCGAGGCGAGC[A/G]GATCACCTGAGGTCA | 124739 |
rs429068 | snp | C/T | 0.487995 | 0.0765403 | intron-variant | USP43 | GRCh38.p7 | 17:9658226 | TAGAATGACGGGCTC[C/T]GAGCAAACACTGAAG | 124739 |
rs430881 | snp | G/T | 0.489837 | 0.0705577 | intron-variant | USP43 | GRCh38.p7 | 17:9694808 | TTTGTATTTTTAGTA[G/T]AGACAGGGTTTCATC | 124739 |
rs437735 | snp | A/G | 0.49533 | 0.0480965 | intron-variant | USP43 | GRCh38.p7 | 17:9714640 | gtgagcttagatcac[A/G]ccactgcactccagc | 124739 |
rs438623 | snp | C/G | | | intron-variant | USP43 | GRCh38.p7 | 17:9725580 | TCAGATCCTGTTATC[C/G]TAGCCCAATTAATGG | 124739 |
rs441285 | snp | A/C | 0.248471 | 0.249995 | intron-variant | USP43 | GRCh38.p7 | 17:9705594 | ACCCTGTCTCTACTA[A/C]AAATACAAAAATCAG | 124739 |
rs444677 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | USP43 | GRCh38.p7 | 17:9708662 | agacggagtctcact[C/G]tgttgcccgggttgg | 124739 |
rs538632 | snp | A/G | 0.491577 | 0.0643472 | intron-variant | USP43 | GRCh38.p7 | 17:9707011 | CCCCAACAATTGGTA[A/G]CTTTCAAGCTGCCAT | 124739 |
rs541413 | snp | C/G | 0.473451 | 0.112115 | intron-variant | USP43 | GRCh38.p7 | 17:9710642 | TGGCACGTGCCTGTA[C/G]TCCCAGCTACTCGGG | 124739 |
rs562919 | snp | A/G | 0.36021 | 0.224397 | intron-variant | USP43 | GRCh38.p7 | 17:9713969 | ttacacacacttgag[A/G]tgaggatggtttggg | 124739 |
rs566011 | snp | A/T | 0.375797 | 0.216044 | intron-variant | USP43 | GRCh38.p7 | 17:9707696 | ttttatttattaaac[A/T]tttttttttaatGCA | 124739 |
rs623661 | snp | A/G | 0.360842 | 0.224085 | intron-variant | USP43 | GRCh38.p7 | 17:9713967 | ttttacacacacttg[A/G]ggtgaggatggtttg | 124739 |
rs687206 | snp | C/T | 0.474091 | 0.11083 | intron-variant | USP43 | GRCh38.p7 | 17:9710664 | CACGTGCCACCACCA[C/T]GCCCAGCTAATTTTT | 124739 |
rs694685 | snp | G/T | 0.323197 | 0.239044 | intron-variant | USP43 | GRCh38.p7 | 17:9713939 | aaaattgtcttccat[G/T]aaaccggtccctggt | 124739 |
rs880334 | snp | A/G | 0.419135 | 0.184101 | intron-variant | USP43 | GRCh38.p7 | 17:9660802 | AGAGGAGCTTACCCC[A/G]CCCTTGGTTTGACCT | 124739 |
rs880335 | snp | A/G | 0.196771 | 0.244268 | intron-variant | USP43 | GRCh38.p7 | 17:9660847 | AAGATCTCTTTCTCT[A/G]TCTGGGGTCAAAGCC | 124739 |
rs882425 | snp | A/G | 0.298651 | 0.24522 | intron-variant | USP43 | GRCh38.p7 | 17:9725011 | TTTTTGGCCAATGAA[A/G]TATGCATCAATCCAT | 124739 |
rs882426 | snp | A/G | 0.456568 | 0.140818 | intron-variant | USP43 | GRCh38.p7 | 17:9724871 | TCAAGGGCTTCCATC[A/G]TGCTTCATACATCTA | 124739 |
rs882427 | snp | C/T | 0.242488 | 0.249887 | intron-variant | USP43 | GRCh38.p7 | 17:9725118 | ACACCCCCTCCACAC[C/T]GCAGCTCTGGAGCCA | 124739 |
rs1110096 | snp | A/T | 0.21725 | 0.247846 | intron-variant | USP43 | GRCh38.p7 | 17:9716485 | ACAGCTTGGAGATAC[A/T]TAGTTCTCTGCACAG | 124739 |
rs1574208 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | USP43 | GRCh38.p7 | 17:9676038 | GGGCCTTCATATGCC[A/G]GTGGGAAGGGGAAGC | 124739 |
rs2139887 | snp | C/T | 0.495445 | 0.0475058 | intron-variant | USP43 | GRCh38.p7 | 17:9684649 | CAGCCTCCCGAGTAG[C/T]TGGGATTACAGGCGT | 124739 |
rs2139888 | snp | C/T | 0.495445 | 0.0475058 | intron-variant | USP43 | GRCh38.p7 | 17:9684620 | GTGAGCCACCATGCC[C/T]GGCTACTTTTGTATT | 124739 |
rs2271003 | snp | A/G | 0.00674831 | 0.0576942 | utr-variant-3-prime, upstream-variant-2KB | CFAP52, USP43 | GRCh38.p7 | 17:9643217 | TGATGAGATGTCTCT[A/G]AGCCTTGGCGTTGCA | 124739 |
rs2315573 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | USP43 | GRCh38.p7 | 17:9676235 | TTCTTAATCAAATAC[G/T]TTTTCCCCCAATTCT | 124739 |
rs2315574 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | USP43 | GRCh38.p7 | 17:9644080 | AGGTAACTGCTGTAA[C/G]CCGGTTTGAAAG | 124739 |
rs2653429 | snp | A/G | 0.35574 | 0.226537 | intron-variant | USP43 | GRCh38.p7 | 17:9704983 | TTTGTTTCATTTTAA[A/G]TGTGGTAATGTGGTA | 124739 |
rs2653441 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | USP43 | GRCh38.p7 | 17:9718031 | tcgatctcttcatct[C/T]gtgatctgcccacct | 124739 |
rs2654717 | snp | A/G | 0.496416 | 0.0421803 | intron-variant | USP43 | GRCh38.p7 | 17:9714552 | gctgggcatggtggc[A/G]cacgcctgtaatccc | 124739 |
rs2654719 | snp | A/G | 0.492727 | 0.0598633 | intron-variant | USP43 | GRCh38.p7 | 17:9662094 | ACAGAGTGGCCAAAG[A/G]CTGAAAACATTTGTG | 124739 |
rs2654723 | snp | A/G | 0.375797 | 0.216044 | intron-variant | USP43 | GRCh38.p7 | 17:9707572 | GAATGGCGTGAACCC[A/G]GGAGGTGGAGCTTGC | 124739 |
rs2654724 | snp | C/G | 0.429087 | 0.174436 | intron-variant | USP43 | GRCh38.p7 | 17:9710210 | GGACCAGGAGAGGTT[C/G]GCAAGGATCTGAAAG | 124739 |
rs2654725 | snp | A/G | 0.435694 | 0.167385 | intron-variant | USP43 | GRCh38.p7 | 17:9711239 | CCTGTTGAACTGTGC[A/G]TGCTGGGGCCCTGGT | 124739 |
rs2684461 | snp | A/G | 0.245631 | 0.249962 | intron-variant | USP43 | GRCh38.p7 | 17:9716616 | GAACCTGCAGAAAGG[A/G]AGAGGTAGTTCCCCC | 124739 |
rs2937968 | snp | C/T | 0.449473 | 0.150701 | intron-variant | USP43 | GRCh38.p7 | 17:9657346 | ctcatttttatatta[C/T]taatagagatggggt | 124739 |
rs2937969 | snp | G/T | 0.477175 | 0.104362 | intron-variant | USP43 | GRCh38.p7 | 17:9709595 | CTGGGTAGCTAGGAT[G/T]ACAGTTGCCTGCCAC | 124739 |
rs2937971 | snp | G/T | 0.190833 | 0.242898 | intron-variant | USP43, LOC107985011 | GRCh38.p7 | 17:9647414 | TCACAAAACTCCAGA[G/T]ACCTTGCTCTTAACC | 124739 |
rs2937975 | snp | A/G | 0.442655 | 0.159323 | intron-variant | USP43 | GRCh38.p7 | 17:9688444 | caacctccgcctccc[A/G]ggttcaagcgattct | 124739 |
rs2956062 | snp | A/G | 0.305186 | 0.243833 | intron-variant | USP43 | GRCh38.p7 | 17:9715242 | ACTTCTTGGACTCAC[A/G]CGATCCTCCCACCTT | 124739 |
rs3066742 | in-del | -/AAAA | | | intron-variant | USP43 | GRCh38.p7 | 17:9717802 | caaaaaaaaaaaaaa[-/AAAA]tgtgagctatacata | 124739 |
rs3744756 | snp | C/T | 0.379436 | 0.213884 | synonymous-codon, utr-variant-5-prime, intron-variant, downstream-variant-500B | USP43, LOC107985011 | GRCh38.p7 | 17:9646124 | CACGCCCCAACTTTC[C/T]GCGGAGTTCAAGGTA | 124739 |
rs3913648 | snp | C/G | 0.49934 | 0.0181589 | intron-variant | USP43 | GRCh38.p7 | 17:9693978 | TAAGCCTCAGGCACA[C/G]TCCACAATCTCTTAC | 124739 |
rs3913649 | snp | C/T | 0.47852 | 0.101384 | intron-variant | USP43 | GRCh38.p7 | 17:9694139 | GAACCTGGGGGTCTA[C/T]GGGAAAATAAAGAGA | 124739 |
rs4101050 | snp | A/C | 0.476401 | 0.106032 | intron-variant | USP43 | GRCh38.p7 | 17:9693702 | TATAGGCGCGTGCTA[A/C]CACGACCGGCTAATT | 124739 |
rs4300688 | snp | A/G | 0.138886 | 0.22395 | intron-variant | USP43 | GRCh38.p7 | 17:9654251 | atatttctactaaaa[A/G]catattcattgttta | 124739 |
rs4791354 | snp | A/G | 0.089084 | 0.191327 | intron-variant | USP43 | GRCh38.p7 | 17:9690794 | ggaggctgaggcaag[A/G]gaatcacttgaactg | 124739 |
rs4791355 | snp | A/G | 0.089084 | 0.191327 | intron-variant | USP43 | GRCh38.p7 | 17:9690840 | tagtgagccgagatc[A/G]caccactgcattcca | 124739 |
rs4791356 | snp | C/T | 0.454784 | 0.1434 | intron-variant | USP43 | GRCh38.p7 | 17:9718310 | tgcaaagatttactA[C/T]ACCAGGCATGTACCA | 124739 |
rs4791357 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | USP43 | GRCh38.p7 | 17:9725634 | TACTTTTTCACTGCC[A/G]TCTCGAGAAAGAGGA | 124739 |
rs4791358 | snp | G/T | 0.238749 | 0.249747 | intron-variant | USP43 | GRCh38.p7 | 17:9725740 | CTTTCCTACCAGGAA[G/T]AAAGGAAGAACTGCT | 124739 |
rs4791856 | snp | A/G | 0.225597 | 0.248806 | intron-variant | USP43 | GRCh38.p7 | 17:9653144 | AGGGACATTTTTAAG[A/G]CCCTATCTTGTCTTG | 124739 |
rs4791857 | snp | C/G | 0.224709 | 0.248717 | intron-variant | USP43 | GRCh38.p7 | 17:9653145 | GGGACATTTTTAAGG[C/G]CCTATCTTGTCTTGC | 124739 |
rs4791858 | snp | A/G | 0.499866 | 0.0081858 | intron-variant | USP43 | GRCh38.p7 | 17:9680829 | AAATTTGAGCAGTAC[A/G]TGGTTAAAGTTTTAT | 124739 |
rs4791859 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | USP43 | GRCh38.p7 | 17:9687901 | AACTCCTCTGCAAGT[A/G]GGTCAGTCTATCCGG | 124739 |
rs4791862 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | USP43 | GRCh38.p7 | 17:9718288 | attaagagcctatcc[G/T]tgatgctgcaaagat | 124739 |
rs4992450 | snp | A/G | 0.5 | 0 | intron-variant | USP43 | GRCh38.p7 | 17:9702632 | GAGTGTTTTCAGAGA[A/G]TGTCATGAGGGATGA | 124739 |
rs5819235 | in-del | -/TATT | 0.00953873 | 0.0683987 | intron-variant | USP43 | GRCh38.p7 | 17:9675951 | TTCGAATCCCAGCTC[-/TATT]AATTAATTACCTGTG | 124739 |
rs5819237 | in-del | -/G | 0 | 0 | intron-variant | USP43 | GRCh38.p7 | 17:9724938 | CTGTGGCGGGGGGCA[-/G]GGGGGCACTAAGCAT | 124739 |
rs6145986 | in-del | -/GAGTGTTTTCAGA | | | intron-variant | USP43 | GRCh38.p7 | 17:9702616 | CATAATCATCCCTTT[-/GAGTGTTTTCAGA]GAGTGTTTTCAGAGA | 124739 |
rs6503237 | snp | A/T | 0.473081 | 0.112848 | intron-variant, upstream-variant-2KB | USP43 | GRCh38.p7 | 17:9669018 | TTTTTTTTTTTTTTT[A/T]AATTTTTAGTAGAGA | 124739 |
rs6503238 | snp | C/T | 0.495291 | 0.0482933 | intron-variant | USP43 | GRCh38.p7 | 17:9678897 | ATATTTCCATTCTTT[C/T]AGTGGTTACTAAAAT | 124739 |
rs6503239 | snp | A/G | 0.499325 | 0.0183582 | intron-variant | USP43 | GRCh38.p7 | 17:9698805 | ATTGAGGCAGAAAGA[A/G]ATGTAAATTTTAGGT | 124739 |
rs6503240 | snp | C/T | 0.384976 | 0.210431 | intron-variant | USP43 | GRCh38.p7 | 17:9722438 | TTCAGTCCATGCCGA[C/T]GTAATGTAACAGCTG | 124739 |
rs6503241 | snp | A/G | 0.386504 | 0.209444 | intron-variant | USP43 | GRCh38.p7 | 17:9722693 | TTCTCTCCTTCCTCC[A/G]ATCAGATGAGAAATA | 124739 |
rs7210230 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | USP43 | GRCh38.p7 | 17:9678635 | gtgagccactgcgcc[C/T]ggccTGTATTTGGAT | 124739 |
rs7211904 | snp | A/G | 0.319376 | 0.240181 | intron-variant | USP43 | GRCh38.p7 | 17:9664880 | CTGACCTCGTGATCC[A/G]CCCACCTCGGTCTCC | 124739 |
rs7212464 | snp | A/G | 0.243919 | 0.249926 | intron-variant | USP43 | GRCh38.p7 | 17:9655521 | TGCAATAAACTTTTA[A/G]AAAGTTGGAATGTAC | 124739 |
rs7214208 | snp | A/G | 0.255224 | 0.249945 | intron-variant | USP43 | GRCh38.p7 | 17:9655535 | AGAAAGTTGGAATGT[A/G]CATTTATGCAGAAAA | 124739 |
rs7216819 | snp | A/T | 0.0463947 | 0.145069 | intron-variant | USP43 | GRCh38.p7 | 17:9687207 | TTTACATTAAAACGA[A/T]ATTTTTTTTTTCACA | 124739 |
rs7216960 | snp | A/C | 0.0627277 | 0.167784 | intron-variant | USP43 | GRCh38.p7 | 17:9665971 | ccttgatttcagtgc[A/C]gtgatactgattttg | 124739 |
rs7217247 | snp | A/C | 0.0872718 | 0.189788 | intron-variant | USP43 | GRCh38.p7 | 17:9689016 | TAGAAATGGATCAAG[A/C]AATCAATGGGGCCAG | 124739 |
rs7217478 | snp | C/T | 0.421051 | 0.182323 | intron-variant | USP43 | GRCh38.p7 | 17:9704246 | attgggacctgcatt[C/T]aggggacctgtgtgt | 124739 |
rs7217807 | snp | A/G | 0.49121 | 0.0657086 | intron-variant | USP43 | GRCh38.p7 | 17:9684052 | TATGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG | 124739 |
rs7219025 | snp | A/C | 0.534248 | 0.11954 | intron-variant | USP43 | GRCh38.p7 | 17:9684115 | GCACTCCAGCCTGGG[A/C]GACAGATCGAGACTG | 124739 |
rs7219195 | snp | G/T | 0.0839998 | 0.186933 | intron-variant | USP43 | GRCh38.p7 | 17:9662011 | TGGAACTGTCAAGAA[G/T]CAGGCAGCTGTGAGG | 124739 |