SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs32453488 | snp | A/G | 0.32 | 0.24 | synonymous-codon | Pex10 | GRCm38.p3 | 4:155070695 | CTGCACCCTATGCTT[A/G]GAGGAACGAAGACAC | 668173 |
rs33122175 | snp | C/G | 0.244898 | 0.249948 | missense | Pex10 | Mm_Celera | 4:155068747 | CCAGGCTCCGCCGTG[C/G]AGCGCTGGTTGCACT | 668173 |
rs33122177 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Pex10 | Mm_Celera | 4:155068850 | TGCTCCCCGGGCTTC[A/G]CAGGGCAGTCTGCTA | 668173 |
rs33122178 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Pex10 | Mm_Celera | 4:155069095 | ATGCCAAGGGGACTG[A/G]TATTCAGGCAGGGAT | 668173 |
rs33122181 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Pex10 | Mm_Celera | 4:155069249 | CCCAGGAAAAGGAAA[A/C]GAAATCCAGTTCCCA | 668173 |
rs33123054 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pex10 | Mm_Celera | 4:155069293 | GCAGCAGACTTGGGT[A/G]CGTGGGCGGGTGACT | 668173 |
rs33123057 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Pex10 | Mm_Celera | 4:155069454 | TTCATCACCATCCAG[A/C]GCCCTAACAGAAAGG | 668173 |
rs33123059 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pex10 | Mm_Celera | 4:155069627 | CACACCAAAGACCTC[A/G]CCCTGGTATCACCTC | 668173 |
rs33123061 | snp | C/G | 0.32 | 0.24 | intron-variant | Pex10 | Mm_Celera | 4:155069646 | TGGTATCACCTCCAT[C/G]CTCACCACCTACCTC | 668173 |
rs33123994 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pex10 | Mm_Celera | 4:155069815 | TGCCCAAGCAGTCAT[C/T]TAGTTTAGCAGATGT | 668173 |
rs33123995 | snp | C/T | 0.32 | 0.24 | intron-variant | Pex10 | Mm_Celera | 4:155069837 | AGCAGATGTGCCTCC[C/T]TTCCCAGTAGCTGCT | 668173 |
rs33123998 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pex10 | Mm_Celera | 4:155070050 | CTTAAGGGCCAGAGT[A/G]TCAGAGGGACAGTAA | 668173 |
rs33123999 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pex10 | Mm_Celera | 4:155070100 | TGCTATTCTCCACCC[C/T]ACTCTTCCTTGGGCT | 668173 |
rs33124002 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Pex10 | Mm_Celera | 4:155070169 | AACCCTCATCCATTT[G/T]CCTGGTCCATCCAGA | 668173 |
rs33125124 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Pex10 | Mm_Celera | 4:155070203 | CTGGGTCTGTGCTGC[G/T]GATGCCTCAAGGTCA | 668173 |
rs33125126 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Pex10 | Mm_Celera | 4:155070392 | GTCTTAACAGCTCCG[C/T]ACTCGTCGCCTGCCT | 668173 |
rs33125128 | snp | A/C | 0.32 | 0.24 | synonymous-codon | Pex10 | Mm_Celera | 4:155070401 | GCTCCGCACTCGTCG[A/C]CTGCCTGGAGAGGAC | 668173 |
rs33125130 | snp | C/G | 0.231111 | 0.249285 | missense | Pex10 | Mm_Celera | 4:155070438 | GCTCGCACTAGCTAC[C/G]GACTGCTGGGGCTGA | 668173 |
rs33125133 | snp | A/G | 0.32 | 0.24 | missense | Pex10 | Mm_Celera | 4:155070490 | TGTCCATGGGGCTGC[A/G]GTTGTACAGCTTCAG | 668173 |
rs33125936 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Pex10 | Mm_Celera | 4:155070545 | GTGGCGGCTGCACCG[C/T]AATCTATCCCACCGC | 668173 |
rs33125940 | snp | A/G | 0.124444 | 0.216185 | missense | Pex10 | Mm_Celera | 4:155070753 | TTCTGCTGGGAGTGC[A/G]TCACCGAGTGGTGCA | 668173 |
rs33125943 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Pex10 | Mm_Celera | 4:155070851 | TCTTGAGTTGGAGAT[A/G]GAGAGGTGGGCATCT | 668173 |
rs33126090 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB | Pex10, Plch2 | Mm_Celera | 4:155065965 | GAGTTCTGGAACCCT[A/G]AAACACTGAAGCAAA | 668173 |
rs33126093 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB | Pex10, Plch2 | Mm_Celera | 4:155066044 | ACAATGATGTCACTA[C/T]TCATCTTGCCCTTCC | 668173 |
rs33126826 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pex10 | Mm_Celera | 4:155070880 | CTGTGAGACATGAAC[C/T]GTGCTTGGGGTTGAA | 668173 |
rs33126828 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pex10 | Mm_Celera | 4:155071029 | ACACACCACTGAACC[A/G]TTTCCAGGACAGGTG | 668173 |
rs33126831 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pex10 | Mm_Celera | 4:155071056 | GGTGCCCAGAACATA[C/T]CGCTTCAGTAAGCAG | 668173 |
rs33126916 | snp | A/T | 0.231111 | 0.249285 | upstream-variant-2KB | Pex10 | Mm_Celera | 4:155066388 | AAAGCAGTCGCGTGT[A/T]AGGAGCAGTCCAGGC | 668173 |
rs33126918 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB | Pex10 | Mm_Celera | 4:155066455 | GTAGAAATGAGCTTC[C/T]AAGTTTGAAAAGTCT | 668173 |
rs33126921 | snp | A/C | 0.244898 | 0.249948 | upstream-variant-2KB | Pex10 | Mm_Celera | 4:155066644 | GCATGGGCAGGGAGG[A/C]ACTCCAACAACTGGA | 668173 |
rs33126923 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB | Pex10 | Mm_Celera | 4:155066787 | CTGCGAGGCTGAGCT[C/T]TCTCGGGGGTCCTAC | 668173 |
rs33127684 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pex10 | Mm_Celera | 4:155071131 | TCCTGGCCAGAAGCC[C/T]AGGCTGCAAGTGAAA | 668173 |
rs33127687 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pex10 | Mm_Celera | 4:155071148 | GGCTGCAAGTGAAAG[A/G]GAATTTTATGTGGCT | 668173 |
rs33127690 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Pex10 | Mm_Celera | 4:155071162 | GGGAATTTTATGTGG[A/C]TGTGCCCTGCTATTA | 668173 |
rs33127693 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Pex10 | Mm_Celera | 4:155071687 | CAGCCAATGTGACAA[A/T]CATACCCTACCCTGC | 668173 |
rs33128094 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB | Pex10 | Mm_Celera | 4:155066849 | CCCGCCACTTCACTG[C/T]GCCGCTTCACCCTCC | 668173 |
rs33128097 | snp | C/G | 0.260355 | 0.249785 | upstream-variant-2KB | Pex10 | Mm_Celera | 4:155067000 | CAGCCCCACGACGGA[C/G]GCACGTCGAGCGTCA | 668173 |
rs33128099 | snp | A/C | 0.124444 | 0.216185 | utr-variant-5-prime | Pex10 | Mm_Celera | 4:155067058 | GCGGTGCGAGCTCTG[A/C]GATTCGGGCCATGGC | 668173 |
rs33128100 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Pex10 | Mm_Celera | 4:155067527 | GGGCTTCTTAAGAGG[C/T]GGTCTTCGTCTCGGA | 668173 |
rs33128101 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Pex10 | Mm_Celera | 4:155067588 | GGTGAAGGGAGAGAC[G/T]AGTTGTTGAGGGTCG | 668173 |
rs33128103 | snp | C/G | 0.124444 | 0.216185 | missense | Pex10 | Mm_Celera | 4:155067857 | ATGGAGGAAAGAGAT[C/G]GAGTTGCTCTCGGAC | 668173 |
rs33128446 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Pex10 | Mm_Celera | 4:155072112 | GGCTCAGGATAGGCT[A/G]GAAGGGAAGTATAAC | 668173 |
rs33128449 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Pex10 | Mm_Celera | 4:155072187 | CCAACTCCCTAAGAA[A/G]ATGATGCCTCAGAGG | 668173 |
rs33128452 | snp | A/G | 0.32 | 0.24 | downstream-variant-500B | Pex10 | Mm_Celera | 4:155072826 | GTGCCACCACTTCCC[A/G]GTAGTCGGTTCTTTG | 668173 |
rs33129435 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Pex10 | Mm_Celera | 4:155068095 | TCCATTTATGGGGTA[C/G]GAGGCAGATAAAAAG | 668173 |
rs33129437 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Pex10 | Mm_Celera | 4:155068246 | TGGTGGAGTACTAGA[A/C]GCTAGCTGCAAGCCA | 668173 |
rs33129439 | snp | A/G | 0.32 | 0.24 | intron-variant | Pex10 | Mm_Celera | 4:155068623 | CAGGCTGGCCCGGAA[A/G]CTTGTCCCTGGACCC | 668173 |
rs46260583 | snp | A/G | | | intron-variant | Pex10 | Mm_Celera | 4:155068592 | GACTGGTGAGGCTGG[A/G]GGGGGGACGACGACA | 668173 |
rs211770014 | snp | A/G | | | intron-variant | Pex10 | Mm_Celera | 4:155069184 | TCCAAGTTGCAATCG[A/G]AATTCTGTACTTGGG | 668173 |
rs212384202 | snp | C/T | | | intron-variant | Pex10 | Mm_Celera | 4:155067639 | GGACTTTACCTGCCC[C/T]TCGGGAGTGACAGGG | 668173 |
rs212722621 | snp | A/G | | | intron-variant | Pex10 | Mm_Celera | 4:155068251 | GAGTACTAGAAGCTA[A/G]CTGCAAGCCATGGGT | 668173 |
rs212793948 | snp | A/G | | | utr-variant-3-prime | Pex10 | Mm_Celera | 4:155072316 | GTGTGCAGGCAGAAC[A/G]CTATAATACATAATA | 668173 |
rs213138830 | snp | A/T | | | intron-variant | Pex10 | Mm_Celera | 4:155071513 | CATAAGTACTGAGGA[A/T]GGGTGGGGTGGGCAC | 668173 |
rs214264010 | snp | G/T | | | upstream-variant-2KB | Pex10 | Mm_Celera | 4:155066128 | TTTGGGTTAACAAGC[G/T]CTAGCAGCCCAAGCT | 668173 |
rs214385863 | snp | C/T | | | intron-variant | Pex10 | Mm_Celera | 4:155069913 | TTCCAGCCCAAGGCA[C/T]GATGTAACCTGGTGT | 668173 |
rs214461895 | snp | A/G | | | intron-variant | Pex10 | Mm_Celera | 4:155067471 | ACTTTCCTGGGCTCC[A/G]TGTCTCTAGGACAGT | 668173 |
rs214636501 | snp | C/T | | | intron-variant | Pex10 | Mm_Celera | 4:155068318 | GCGTCAGGTAAGCAG[C/T]GGTATGTATGCCTGA | 668173 |
rs214747257 | snp | A/T | | | synonymous-codon | Pex10 | Mm_Celera | 4:155068892 | CAGCCGATCAGGGGC[A/T]CGGCGCTGGGTGCGT | 668173 |
rs215142535 | snp | C/T | | | upstream-variant-2KB | Pex10, Plch2 | Mm_Celera | 4:155065594 | GCCAGAGCTGGCAAA[C/T]GACATCAGGCAGGAC | 668173 |
rs215359002 | snp | C/T | | | downstream-variant-500B | Pex10 | GRCm38.p3 | 4:155072593 | AAAAAAGGGAACTGA[C/T]TCCTGCAAGTTGTTC | 668173 |
rs216282882 | snp | C/T | | | upstream-variant-2KB | Pex10 | Mm_Celera | 4:155066905 | GTAGCCCCACCCCTA[C/T]GTCGTGGACACGCCC | 668173 |
rs216900966 | snp | A/G | | | intron-variant | Pex10 | Mm_Celera | 4:155069712 | CCCTCCAGCCAGTGC[A/G]CTCCTCCCACACTCA | 668173 |
rs217591379 | snp | A/G | | | upstream-variant-2KB | Pex10, Plch2 | Mm_Celera | 4:155065947 | CGCTCTACCTCCACC[A/G]CAGAGTTCTGGAACC | 668173 |
rs217981009 | snp | A/G | | | intron-variant | Pex10 | Mm_Celera | 4:155071250 | AGCAGTCTGCATAGT[A/G]GGCACTGTGTACCAG | 668173 |
rs218073709 | snp | A/G | | | intron-variant | Pex10 | Mm_Celera | 4:155070569 | CCACCGCAGGTGTGC[A/G]GGGAGCTTGAGGTAC | 668173 |
rs218544834 | in-del | -/G | | | upstream-variant-2KB | Pex10 | Mm_Celera | 4:155066096 | GCCTCTTGTTTCCCT[-/G]ATCTGTGCAGGATCT | 668173 |
rs218626570 | in-del | -/GCATGTTGGGT | | | intron-variant | Pex10 | Mm_Celera | 4:155070943 | GGGCAGGTGAATGGC[-/GCATGTTGGGT]GCACATATCAGGCTA | 668173 |
rs218895552 | snp | A/C | | | upstream-variant-2KB | Pex10 | Mm_Celera | 4:155066769 | ATCAGGCCAAAAACA[A/C]ATCTGCGAGGCTGAG | 668173 |
rs219519883 | in-del | -/GCATGTCCAGCCAGTCA | | | intron-variant | Pex10 | Mm_Celera | 4:155071086 | GCCGGGCCCTGGCTG[-/GCATGTCCAGCCAGTCA]GCTACTTTTACTGTC | 668173 |
rs219636564 | snp | C/G | | | utr-variant-3-prime | Pex10 | Mm_Celera | 4:155072117 | AGGATAGGCTGGAAG[C/G]GAAGTATAACACTCT | 668173 |
rs219977178 | snp | A/T | | | intron-variant | Pex10 | Mm_Celera | 4:155068625 | GGCTGGCCCGGAAAC[A/T]TGTCCCTGGACCCTC | 668173 |
rs220017080 | snp | A/G | | | intron-variant | Pex10 | Mm_Celera | 4:155069280 | CAGACTGAAGGTGGC[A/G]GCAGACTTGGGTGCG | 668173 |
rs220102123 | snp | A/C | | | intron-variant | Pex10 | Mm_Celera | 4:155068439 | ACTGGAAAACAGAAT[A/C]AAGACTTAAGGGAGT | 668173 |
rs220376182 | snp | C/T | | | intron-variant | Pex10 | Mm_Celera | 4:155067783 | GTCATCTTAAGAGAA[C/T]CACTTCACCTCTCTA | 668173 |
rs221113135 | snp | A/G | | | intron-variant | Pex10 | Mm_Celera | 4:155070878 | ATCTGTGAGACATGA[A/G]CCGTGCTTGGGGTTG | 668173 |
rs221288931 | snp | C/T | | | intron-variant | Pex10 | Mm_Celera | 4:155070156 | CAGACAGCTCTAGAA[C/T]CCTCATCCATTTGCC | 668173 |
rs221512198 | snp | C/T | | | intron-variant | Pex10 | Mm_Celera | 4:155067752 | AAAGGCGTGTGCCAC[C/T]ACTACCCGGCTGGGA | 668173 |
rs221575094 | snp | C/T | | | intron-variant | Pex10 | Mm_Celera | 4:155068383 | AGCCACAAGATCGGA[C/T]CCCATCACTTGGACA | 668173 |
rs221637171 | snp | A/C | | | upstream-variant-2KB | Pex10, Plch2 | Mm_Celera | 4:155065053 | CCTTGCCAGACTCCA[A/C]ACTTGCAGGCGTACA | 668173 |
rs221678197 | snp | A/G | | | upstream-variant-2KB | Pex10 | Mm_Celera | 4:155066309 | GGCCGTATCCCTGAG[A/G]ACAACAGATACTTGA | 668173 |
rs221832139 | snp | C/T | | | intron-variant | Pex10 | Mm_Celera | 4:155070838 | AATCTCCCAAACCTC[C/T]TGAGTTGGAGATAGA | 668173 |
rs221849353 | snp | A/G | | | intron-variant | Pex10 | Mm_Celera | 4:155067673 | CTCTGTGTAGCCCTG[A/G]CTGTCCTGGAACTCA | 668173 |
rs225546704 | in-del | -/GGCC | | | intron-variant | Pex10 | Mm_Celera | 4:155068598 | GAGGCTGGAGGGGGG[-/GGCC]ACGACGACACAGGCT | 668173 |
rs225683989 | snp | C/T | | | utr-variant-3-prime | Pex10 | Mm_Celera | 4:155072363 | AAGAAAAATAGAAAA[C/T]GAAGGTCTTCATCTT | 668173 |
rs226214336 | snp | C/T | | | intron-variant | Pex10 | Mm_Celera | 4:155067488 | GTCTCTAGGACAGTA[C/T]CTGACTCAAGACAGT | 668173 |
rs226279330 | snp | A/T | | | intron-variant | Pex10 | Mm_Celera | 4:155068083 | AGGATGGGCTTTTCC[A/T]TTTATGGGGTACGAG | 668173 |
rs226584669 | snp | C/T | | | utr-variant-3-prime | Pex10 | Mm_Celera | 4:155072213 | AGAGGCTAAGAGCAC[C/T]GGATGTTCTGCAGAA | 668173 |
rs227175232 | snp | C/T | | | utr-variant-3-prime | Pex10 | Mm_Celera | 4:155071967 | GTCACATGTAATTTA[C/T]AGCTTCTTCAGTCTC | 668173 |
rs227232394 | in-del | -/AAAA | | | upstream-variant-2KB | Pex10, Plch2 | Mm_Celera | 4:155065550 | AAATAAATCTTTAAG[-/AAAA]AAAAAAAAAAAAAGA | 668173 |
rs227564735 | snp | C/T | | | intron-variant | Pex10 | Mm_Celera | 4:155070882 | GTGAGACATGAACCG[C/T]GCTTGGGGTTGAAGT | 668173 |
rs227680138 | snp | C/T | | | synonymous-codon | Pex10 | Mm_Celera | 4:155068922 | TCACCACGCAGCCAC[C/T]CTGACTGAACAACAG | 668173 |
rs227689520 | snp | A/C | | | intron-variant | Pex10 | Mm_Celera | 4:155069707 | CCTCTCCCTCCAGCC[A/C]GTGCGCTCCTCCCAC | 668173 |
rs228036465 | snp | A/G | | | intron-variant | Pex10 | Mm_Celera | 4:155067315 | CCCATTTATTCTCCA[A/G]ACGCCCCTACAGGGT | 668173 |
rs228048550 | snp | A/G | | | upstream-variant-2KB | Pex10 | Mm_Celera | 4:155066714 | AGATCCACTTTTGCA[A/G]CCCAGAGACACGTAC | 668173 |
rs228091437 | snp | C/T | | | intron-variant | Pex10 | Mm_Celera | 4:155067253 | AACAGAGGTACACAC[C/T]GCTGACCACATTGCA | 668173 |
rs228479352 | snp | A/G | | | intron-variant | Pex10 | Mm_Celera | 4:155071051 | GGACAGGTGCCCAGA[A/G]CATACCGCTTCAGTA | 668173 |
rs228582624 | snp | G/T | | | intron-variant | Pex10 | Mm_Celera | 4:155068224 | AAGTCAGGATTCATC[G/T]TCTGCATGGTGGAGT | 668173 |
rs228599077 | snp | A/G | | | synonymous-codon | Pex10 | Mm_Celera | 4:155068811 | ACTGCTGCCCCTGGA[A/G]CAGGAGCTGCAAGCC | 668173 |
rs228913928 | snp | C/T | | | intron-variant | Pex10 | Mm_Celera | 4:155069675 | TCACCTGTCAGGGGA[C/T]CAAATGCCACCTCTC | 668173 |
rs228962145 | in-del | -/G | | | intron-variant | Pex10 | Mm_Celera | 4:155067565 | CGGTCACCAAGGGCA[-/G]CAGAGGAGGTGAAGG | 668173 |