SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6173659 | snp | G/T | 0.304688 | 0.243945 | intron-variant | Usp42 | Mm_Celera | 5:143719965 | CTAAGGAAGGGCTTT[G/T]AGGAAGGGACTTGCA | 76800 |
rs6374512 | snp | C/T | 0.5 | 0 | intron-variant | Usp42 | Mm_Celera | 5:143749641 | tggccactggacttt[C/T]ccctgttttcttggg | 76800 |
rs6375025 | snp | C/T | 0.5 | 0 | intron-variant | Usp42 | Mm_Celera | 5:143749721 | gtttccccTGGTGCT[C/T]GGTCTTCCCTCCTTT | 76800 |
rs6376051 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Usp42 | Mm_Celera | 5:143749891 | AATCTGAGATCTCCC[A/G]CAGCTCTGCCCNGAT | 76800 |
rs6376075 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Usp42 | Mm_Celera | 5:143749903 | CCCNCAGCTCTGCCC[C/T]GATTGAGTGACATCT | 76800 |
rs13471220 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Cyth3, Usp42 | Mm_Celera | 5:143709942 | CAGAGCTACAGGTGT[A/G]CTTTGCTGACAAGTT | 76800 |
rs13478573 | snp | C/T | 0.421265 | 0.182122 | intron-variant | Usp42 | Mm_Celera | 5:143752886 | CAGGATGAACAGGGA[C/T]GTCTTCATGCCCCTC | 76800 |
rs29508713 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp42 | GRCm38.p3 | 5:143749620 | AGCTGGAGTGCAGGT[A/G]TGTGCTGGCCACTGG | 76800 |
rs29514187 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Usp42 | Mm_Celera | 5:143737126 | TTTCATCTTAAAAAA[A/T]ATATATTTTTTTCTG | 76800 |
rs29524237 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp42 | Mm_Celera | 5:143743149 | TGCATTCTCTCCTAG[C/T]ACCCAGTGAATGCTG | 76800 |
rs29527812 | snp | C/T | 0.495 | 0.0497494 | intron-variant | Usp42 | GRCm38.p3 | 5:143711409 | ACTCTCTGGATGTGT[C/T]CCCAAGGCTTTTGAA | 76800 |
rs29543366 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Usp42 | Mm_Celera | 5:143719637 | GGTGGTAAGTGCACT[C/T]AGTCTGATGTCATTC | 76800 |
rs29544467 | snp | G/T | 0.375 | 0.216506 | intron-variant | Usp42 | GRCm38.p3 | 5:143730737 | TTATCTTTCTCATTT[G/T]AAGAAAGAATATCAC | 76800 |
rs29566210 | snp | A/G | 0.48 | 0.0979796 | upstream-variant-2KB, intron-variant, nc-transcript-variant | Usp42, LOC105242559 | GRCm38.p3 | 5:143733707 | TTAGGCAGAAGGATT[A/G]CCATGAGTTCAAGCC | 76800 |
rs29579736 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | D130017N08Rik, Usp42 | GRCm38.p3 | 5:143760655 | AACCAAGGGATGGGA[A/G]GAGTTGGTTTCAGTG | 76800 |
rs29580698 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp42 | GRCm38.p3 | 5:143724728 | TCTTGCCAGCTCAGT[A/G]TTTCTTAATAAAACA | 76800 |
rs29581765 | snp | A/T | 0.359862 | 0.224567 | intron-variant, utr-variant-5-prime | D130017N08Rik, Usp42 | Mm_Celera | 5:143759787 | GTGTAGGTGAGGACC[A/T]ACCAAGTGAGGGTTC | 76800 |
rs29583080 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp42 | Mm_Celera | 5:143718313 | AGACTAGGCTTCAAA[C/T]ATATAGAGATGCCTC | 76800 |
rs29618996 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Usp42 | Mm_Celera | 5:143743023 | CCTCCTTAATGCTCC[A/G]AGGGCTTTTCATAAA | 76800 |
rs29633763 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Usp42 | Mm_Celera | 5:143720473 | TCTAAAACACCTTAC[A/G]TTAAGATTTTAAAAC | 76800 |
rs29679413 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp42 | GRCm38.p3 | 5:143730558 | AAAACGGCCTGTGAA[C/T]GGTAACTACTTACTC | 76800 |
rs29732563 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Usp42 | GRCm38.p3 | 5:143753663 | TTTAGTCGGCAGATT[A/G]CTAGTCTAGCACGCA | 76800 |
rs33060123 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Usp42 | Mm_Celera | 5:143738991 | AACAAAAAAGTAGAG[A/G]AAGTAACTTGGAAGG | 76800 |
rs33085154 | snp | A/G | 0.359862 | 0.224567 | utr-variant-3-prime | Usp42 | Mm_Celera | 5:143710776 | GGTAAATTGATTGGA[A/G]TAGTTCCACAAAGTT | 76800 |
rs33088402 | snp | A/G | 0.5 | 0 | intron-variant | Usp42 | Mm_Celera | 5:143751603 | AATGCCAGTGGGTGC[A/G]AGGTGGGTGGGTAAG | 76800 |
rs33137321 | snp | C/T | 0.5 | 0 | intron-variant | Usp42 | Mm_Celera | 5:143754552 | GGGGCATGAAACAGA[C/T]GATAACCCAAGTATC | 76800 |
rs33147319 | snp | A/G | 0.35503 | 0.226867 | intron-variant | D130017N08Rik, Usp42 | Mm_Celera | 5:143759141 | TGCCTCTCATCCTGC[A/G]TAAGTGCTGGGAATT | 76800 |
rs33147943 | snp | G/T | 0.375 | 0.216506 | intron-variant | Usp42 | GRCm38.p3 | 5:143713294 | ATATCCTCCTGTGCC[G/T]TTTTGATTTTGTTTT | 76800 |
rs33177164 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Usp42 | GRCm38.p3 | 5:143722666 | TCGAGCCAATCCTAT[A/G]ACCGGGAAAGACTGA | 76800 |
rs33178832 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp42 | Mm_Celera | 5:143756263 | TCCCTCTGTATCTCC[A/G]AGCATGTGTGCCCAT | 76800 |
rs33193878 | snp | G/T | 0.375 | 0.216506 | intron-variant | Usp42 | GRCm38.p3 | 5:143718264 | CCCCCTAAGACACAC[G/T]ATACGGCCCTGGCTA | 76800 |
rs33276293 | snp | C/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | D130017N08Rik, Usp42 | Mm_Celera | 5:143761174 | CAAAAGGAAATTACT[C/G]TCTCGTTAGCAATTA | 76800 |
rs33290137 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp42 | GRCm38.p3 | 5:143736188 | TCAAACGTAAGCATC[C/T]TGAATTTTGGGCTTA | 76800 |
rs33301512 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Usp42 | GRCm38.p3 | 5:143711373 | TGCAGCAGGCATTAG[A/C]CGAACAGAGGTTGGT | 76800 |
rs33364958 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Usp42 | GRCm38.p3 | 5:143714546 | AGAGTGAAACAAAGA[C/T]ACTGCTGGCTTGGTG | 76800 |
rs33404014 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | D130017N08Rik, Usp42 | GRCm38.p3 | 5:143760773 | GCGGAAGGAGCACTG[A/G]CTTAGAGGCTAGCCT | 76800 |
rs33436692 | snp | A/T | 0.375 | 0.216506 | intron-variant | Usp42 | Mm_Celera | 5:143744928 | AAGTAATTCTTTTTT[A/T]AAAAAAAAGTCTCTG | 76800 |
rs33443022 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Usp42, LOC105242559 | Mm_Celera | 5:143733006 | CACTGCTGATCAAAA[C/T]CTTTCACCCCCTAGA | 76800 |
rs33503204 | snp | A/G | 0.5 | 0 | intron-variant | Usp42 | Mm_Celera | 5:143745575 | CACTTGATCCAAACC[A/G]GGAAACCTCGTATGC | 76800 |
rs33560354 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | D130017N08Rik, Usp42 | Mm_Celera | 5:143760040 | TCTACTCTGGTGTCT[C/T]GAACGTATCTTACAG | 76800 |
rs33560583 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Usp42 | Mm_Celera | 5:143723760 | GTAAGAAGAAAAAAG[C/T]GCATACAAGCCCCGC | 76800 |
rs33587458 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp42 | GRCm38.p3 | 5:143741586 | AGAGCAGCTGAGGCT[C/T]GGCACTGTGAGAGGC | 76800 |
rs33600501 | snp | A/C | 0.375 | 0.216506 | intron-variant | Usp42 | GRCm38.p3 | 5:143716222 | CTCATTCAGTAAAAA[A/C]TAAAACTTGTAGCAA | 76800 |
rs33600997 | snp | A/C | 0.444444 | 0.157135 | intron-variant, downstream-variant-500B | Usp42, LOC105242559 | GRCm38.p3 | 5:143735963 | CTCACTTTGTAGACC[A/C]GGCTGGCCTCGAACT | 76800 |
rs33611705 | snp | A/G | 0.444444 | 0.157135 | missense | Usp42 | Mm_Celera | 5:143718007 | GCTGACTGACTCCTG[A/G]GCGGGGAGAGGATTG | 76800 |
rs33622458 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Usp42 | Mm_Celera | 5:143747005 | TTTACCATCTTACTT[C/T]GGACCTCTCCTTCCT | 76800 |
rs33625434 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Usp42 | Mm_Celera | 5:143729695 | AATTCTTTAAAACCT[A/C]TGAATTAAAGGGAGT | 76800 |
rs33638155 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Usp42 | GRCm38.p3 | 5:143728993 | AAATTTTCATGATAA[A/C]CCTTTGGAAGATCAG | 76800 |
rs33655652 | snp | C/T | 0.5 | 0 | intron-variant | Usp42 | Mm_Celera | 5:143738578 | TCCATGGCCAACCTA[C/T]ATGAGAAGGTGATGT | 76800 |
rs33686649 | snp | A/G | 0.33241 | 0.236027 | upstream-variant-2KB, intron-variant | D130017N08Rik, Usp42 | Mm_Celera | 5:143758209 | CTATCTCCACCAGGC[A/G]CAAGAGGCCAATGTG | 76800 |
rs33693278 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp42 | Mm_Celera | 5:143724562 | TATCTCTTATGTCTT[A/G]TGTATGTGTTACGTT | 76800 |
rs33698131 | snp | A/T | 0.5 | 0 | intron-variant | Usp42 | GRCm38.p3 | 5:143724799 | CTACAAATCCTGACA[A/T]GTATTTTCAATTTCC | 76800 |
rs33722194 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp42 | Mm_Celera | 5:143727648 | ACATGGTAATAATGA[C/T]CTGTGGGTGGGTGTG | 76800 |
rs33756358 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp42 | GRCm38.p3 | 5:143749158 | ATAAATGCAATAAAA[C/T]GCTTTTTAATAACTG | 76800 |
rs45654265 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp42 | Mm_Celera | 5:143751429 | AACTTTGCCACACCA[C/T]TTGCAGCATCTTTGT | 76800 |
rs45657795 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Usp42 | GRCm38.p3 | 5:143723630 | AGGAAAAGCAAAAAG[C/T]ACATCATCCAGTGGG | 76800 |
rs45696010 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp42 | Mm_Celera | 5:143724059 | TGTGCAACAGGAAGG[C/T]AGAGCAGAGATGAGG | 76800 |
rs45705868 | snp | C/T | | | missense | Usp42 | Mm_Celera | 5:143714908 | CTGTTGAAGTGGGGC[C/T]GTTCCTTCCCCCGGG | 76800 |
rs45783494 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp42 | Mm_Celera | 5:143719367 | GGCCTCCTTGTGCTC[A/G]GGTGCATGGCAACTC | 76800 |
rs45787681 | snp | A/G | 0.493827 | 0.0552116 | upstream-variant-2KB, intron-variant | D130017N08Rik, Usp42 | Mm_Celera | 5:143756625 | AATGAGTGTCAGTCC[A/G]TGTGCCTGGGGATGA | 76800 |
rs45808070 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Usp42 | Mm_Celera | 5:143752083 | TTTCTCTCATACCTG[A/G]GTGTGCTAAGCAGAC | 76800 |
rs45951358 | snp | A/G | 0.18 | 0.24 | intron-variant, upstream-variant-2KB | D130017N08Rik, Usp42 | GRCm38.p3 | 5:143761501 | CAGGCAATCATGACT[A/G]TAGTCGAGACTTGAG | 76800 |
rs46027225 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Usp42 | GRCm38.p3 | 5:143723667 | AACACACACCTACGC[C/T]CTGTGCTTGGGATGT | 76800 |
rs46050562 | snp | A/C | | | intron-variant | Usp42 | GRCm38.p3 | 5:143723686 | TGCTTGGGATGTGGG[A/C]ATCAGAGGAGTCAGG | 76800 |
rs46052172 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp42 | Mm_Celera | 5:143754982 | GAAGGGCATCGTGAC[A/G]ACGTTAAGGTCGGTT | 76800 |
rs46060680 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Usp42 | Mm_Celera | 5:143724169 | TTCATCTAGGACACC[A/G]AGGGATGAGTATAGC | 76800 |
rs46139508 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp42 | Mm_Celera | 5:143751689 | CTGAGCACACCAATG[A/G]GCCTCCTAAGAGGAA | 76800 |
rs46203669 | snp | C/G | | | intron-variant | Usp42 | GRCm38.p3 | 5:143725324 | GCGTGCAGCCTCAAG[C/G]TCCAGTACCAAAACA | 76800 |
rs46309393 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp42 | Mm_Celera | 5:143713879 | CACCGAGGGAAACTG[C/T]CATCTACGCTCCCTG | 76800 |
rs46323138 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp42 | Mm_Celera | 5:143720187 | TTGCACATGACTGTG[C/T]ATCTTGACCACTTTA | 76800 |
rs46388026 | snp | A/G | 0.244898 | 0.249948 | upstream-variant-2KB, intron-variant | D130017N08Rik, Usp42 | Mm_Celera | 5:143756617 | AATCAAATAATGAGT[A/G]TCAGTCCGTGTGCCT | 76800 |
rs46442388 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp42 | Mm_Celera | 5:143737395 | TGTATGCTAAGCTAA[C/T]TGCCCCAGCAGACTG | 76800 |
rs46492651 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp42 | Mm_Celera | 5:143738554 | TGTCAGAATGAGAGA[C/T]GCAGGGAGTCCATGG | 76800 |
rs46492724 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Usp42 | Mm_Celera | 5:143737936 | AGACCCACCAAGTGT[C/T]CAACTTACCTCAAGA | 76800 |
rs46611965 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp42 | Mm_Celera | 5:143753414 | TAAGAAAGGACTTTA[A/G]GAGTGAGTGAGTGAG | 76800 |
rs46633323 | snp | A/G | | | intron-variant | Usp42 | GRCm38.p3 | 5:143727277 | CACACACAAACGAGG[A/G]AGGTCTGTGGTTGGA | 76800 |
rs46635862 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Usp42 | Mm_Celera | 5:143755628 | TGTGTGTGTAGTGTG[C/T]GTGCAGAAGTATCTA | 76800 |
rs46655294 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Usp42 | Mm_Celera | 5:143722654 | ACCAGCGTTTGCTCG[A/G]GCCAATCCTATAACC | 76800 |
rs46691539 | snp | A/G | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | D130017N08Rik, Usp42 | GRCm38.p3 | 5:143761270 | TATATACTTACATAT[A/G]TTTATTGGTCTTAAC | 76800 |
rs46710098 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp42 | Mm_Celera | 5:143714006 | CACCACCACTTTCCC[C/T]AGCCATGTCTGCCCA | 76800 |
rs46713573 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp42 | Mm_Celera | 5:143716159 | ACTCAACTACTTGCA[A/G]CTTAAGCATATCTGA | 76800 |
rs46761655 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp42 | Mm_Celera | 5:143749725 | CCCCTGGTGCTCGGT[C/T]TTCCCTCCTTTTGAG | 76800 |
rs46765554 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp42 | Mm_Celera | 5:143712054 | TAACGATAATCAGTT[C/T]CTACAGCTCATTATC | 76800 |
rs46804044 | snp | C/T | | | intron-variant, upstream-variant-2KB | D130017N08Rik, Usp42 | GRCm38.p3 | 5:143761341 | ACCATGCATAGCAGT[C/T]AGTTAGTGGTACTAC | 76800 |
rs46814352 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Usp42 | Mm_Celera | 5:143750913 | CCTGGGACTCAAACC[C/T]GGGTCCTCATGCTTG | 76800 |
rs46833730 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Usp42 | Mm_Celera | 5:143746311 | TGTCCTCTTTTGTAA[C/T]ATAAGGAAGTACCTG | 76800 |
rs46865586 | snp | C/G | 0.124444 | 0.216185 | synonymous-codon | Usp42 | Mm_Celera | 5:143719832 | GGGCTGAGACATATA[C/G]GGCCGGATATCAAGG | 76800 |
rs46955920 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Usp42 | GRCm38.p3 | 5:143714020 | CCAGCCATGTCTGCC[A/C]AGTGTTCAAGCAGAG | 76800 |
rs47078801 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Usp42 | GRCm38.p3 | 5:143713537 | CTTGCTTCCCTTACC[C/T]TGGCCATACTCCGAC | 76800 |
rs47175743 | snp | A/G | | | intron-variant | Usp42 | Mm_Celera | 5:143736715 | CATCCCTACAACAGC[A/G]GAAGGAGACAAGTGC | 76800 |
rs47195875 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Usp42 | GRCm38.p3 | 5:143714420 | AGGCAGAGAAGAAAC[G/T]GCAACAGTTACAAGA | 76800 |
rs47222152 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Usp42 | Mm_Celera | 5:143752440 | TATGTGTGTCACTGT[A/G]GGTCCCATTGGGTCC | 76800 |
rs47315747 | snp | C/T | 0.124444 | 0.216185 | missense | Usp42 | Mm_Celera | 5:143716983 | GCCTATCGGAGTGAG[C/T]GCCGGCCATCATGTC | 76800 |
rs47380813 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp42 | Mm_Celera | 5:143743625 | TCGTCCTCAGATGGC[C/T]GTCTTTATTATCCAT | 76800 |
rs47434564 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp42 | Mm_Celera | 5:143720408 | AAGCACAAGAAGGAA[A/G]GGTTGGGATACTCAG | 76800 |
rs47494611 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp42 | Mm_Celera | 5:143745666 | CCAGGTCTCCTCTAG[A/G]TCACCTTGCTGAGGC | 76800 |
rs47511627 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp42 | Mm_Celera | 5:143755408 | CTGGCCCGTGGTACT[C/T]CCTCGGTTTTCAAAT | 76800 |
rs47521372 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp42 | Mm_Celera | 5:143750696 | GGACTGTGTTCATCC[C/T]TTTTGTTCTTTGTGC | 76800 |
rs47605409 | snp | C/T | 0.277778 | 0.248452 | intron-variant, upstream-variant-2KB | D130017N08Rik, Usp42 | GRCm38.p3 | 5:143761401 | CCCATGCAGAGCAGT[C/T]AGTTAGTGGTACTAC | 76800 |
rs47631190 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Usp42 | Mm_Celera | 5:143754463 | CCCCCTGGGGCTGAA[A/C]GGTCTTTACCACCCT | 76800 |