SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6298739 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | Pex2 | Mm_Celera | 3:5577138 | CAGTGTAGAAAACAC[A/T]GTANGAGGAGCTCCA | 19302 |
rs6298741 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Pex2 | Mm_Celera | 3:5577142 | GTAGAAAACACNGTA[A/G]GAGGAGCTCCAGTTT | 19302 |
rs6298796 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Pex2 | Mm_Celera | 3:5577172 | TGCTACAGTAGGTAT[A/G]GAATACAGATAGGGA | 19302 |
rs6299304 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Pex2 | Mm_Celera | 3:5577235 | ACCCACCCCATGGTG[A/G]CCACTATCTTCTTGT | 19302 |
rs6299926 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Pex2 | Mm_Celera | 3:5577395 | AAGTAATGGGGTTCC[C/T]ATTATTATGTAGGGA | 19302 |
rs6300469 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Pex2 | Mm_Celera | 3:5577491 | AGCCCAAGGTAGGCT[A/G]TGATAGACTGTTTAG | 19302 |
rs6300923 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Pex2 | Mm_Celera | 3:5577534 | tttgcttttgatacg[A/G]gcttttgcantgtag | 19302 |
rs6300946 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Pex2 | Mm_Celera | 3:5577544 | atacgngcttttgca[A/G]tgtagctctatggtt | 19302 |
rs6313676 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Pex2 | Mm_Celera | 3:5577601 | gctatgtgctgggaa[A/G]acaACTGCATATTTT | 19302 |
rs6313706 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | Pex2 | Mm_Celera | 3:5577620 | ACTGCATATTTTCTT[G/T]CCTAGTTCACTTGAT | 19302 |
rs6313755 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | Pex2 | Mm_Celera | 3:5577656 | TGAGGACAAAGGTGA[A/C]attaaaaaaaaataa | 19302 |
rs6321573 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Pex2 | Mm_Celera | 3:5572503 | GCACTTGTTTCAGTA[A/C]GTAAGGTTAACTAAA | 19302 |
rs30015309 | snp | C/G | 0.375 | 0.216506 | utr-variant-5-prime, upstream-variant-2KB | Pex2 | GRCm38.p3 | 3:5576220 | CCCAGAAGCAACACC[C/G]GGTCTGAGGAAAGCC | 19302 |
rs30022525 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pex2 | GRCm38.p3 | 3:5567258 | TCTATCCATTTGCCT[A/G]AAAATTTCATGATGT | 19302 |
rs30072921 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Pex2 | GRCm38.p3 | 3:5570695 | CTAAAAAAAGTCAAC[C/T]TCAATCATTTTGCTT | 19302 |
rs30165881 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Pex2 | Mm_Celera | 3:5567915 | CCTCTGGGTTAGTCA[C/G]TTACAAAACAAAATT | 19302 |
rs30204798 | snp | A/C | 0.375 | 0.216506 | intron-variant, utr-variant-5-prime | Pex2 | GRCm38.p3 | 3:5575793 | CTAGTACTGTTCTAA[A/C]GGCGAGGAGGCGCTT | 19302 |
rs30211066 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pex2 | GRCm38.p3 | 3:5567526 | AATCGATTTCCAAAG[C/T]TTGTACCCCTACCAG | 19302 |
rs30256328 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Pex2 | GRCm38.p3 | 3:5565388 | AGGGTCAGTATGGTT[A/G]CAGCAACTAAACCCA | 19302 |
rs30308135 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Pex2 | GRCm38.p3 | 3:5565514 | TACTCATTAGAACAG[A/G]TTTCTGCTGGCTGTG | 19302 |
rs30427963 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pex2 | GRCm38.p3 | 3:5563795 | GTTGATCCTCCTATA[A/G]GGTTGCCGACCCCTT | 19302 |
rs30503767 | snp | A/T | 0.359862 | 0.224567 | intron-variant | Pex2 | Mm_Celera | 3:5565102 | CAAAATTATTTCCAA[A/T]TACCATTAAAAAATA | 19302 |
rs30650289 | snp | C/T | 0.32 | 0.24 | intron-variant | Pex2 | GRCm38.p3 | 3:5564149 | TCTTCTTGAGTTTCA[C/T]GTGCTTTGTAAATTG | 19302 |
rs30810651 | snp | A/C/G | 0.444444 | 0.157135 | intron-variant | Pex2 | GRCm38.p3 | 3:5572364 | AACACACATATGTAT[A/C/G]TATTTCCCCCTCTTT | 19302 |
rs30854366 | snp | G/T | 0.32 | 0.24 | intron-variant | Pex2 | GRCm38.p3 | 3:5564278 | TATGTAGCAGAGAAT[G/T]GCCTAGTCGGCCATC | 19302 |
rs30948395 | snp | A/G | 0.32 | 0.24 | intron-variant | Pex2 | Mm_Celera | 3:5564361 | GAATGCCAGGGCCAG[A/G]AAATGGGAGTAGGTG | 19302 |
rs30985122 | snp | A/C | 0.387812 | 0.208586 | intron-variant | Pex2 | Mm_Celera | 3:5571096 | AAGGTCCCCTGCTGA[A/C]ATTTTATCAGGGTAC | 19302 |
rs31335996 | snp | C/G | 0.375 | 0.216506 | intron-variant | Pex2 | GRCm38.p3 | 3:5567586 | TTGGGCCAGCACAAG[C/G]TGCTATGCCTTGAGT | 19302 |
rs31722085 | snp | A/G | 0.375 | 0.216506 | intron-variant | Pex2 | GRCm38.p3 | 3:5567446 | GGTAGAGCATCTTTT[A/G]GGGATATGCCCAAAA | 19302 |
rs31722903 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Pex2 | Mm_Celera | 3:5562240 | GGAGAAAGCTGAACT[A/G]CACAGAACATGGCTA | 19302 |
rs31738191 | snp | A/G | 0.375 | 0.216506 | intron-variant | Pex2 | GRCm38.p3 | 3:5567307 | AGTAATACTCCATTG[A/G]GTAGATGCACCACAT | 19302 |
rs33275924 | snp | C/T | 0.32 | 0.24 | intron-variant | Pex2 | Mm_Celera | 3:5563070 | CTACTAAGACTGGGC[C/T]AAAACACAGTAAGGA | 19302 |
rs33275926 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Pex2 | Mm_Celera | 3:5563123 | ACACATTGTCCAGCC[A/T]TTGAGAGGCCCAAGC | 19302 |
rs33275929 | snp | A/G | 0.32 | 0.24 | intron-variant | Pex2 | Mm_Celera | 3:5563151 | AGCCAGCAACACACA[A/G]AACCAAGACTTACAC | 19302 |
rs33275932 | snp | A/T | 0.32 | 0.24 | utr-variant-5-prime | Pex2 | Mm_Celera | 3:5563198 | GTGGACATCAACTGT[A/T]GCCAATGTGATTTGA | 19302 |
rs33276805 | snp | C/T | 0.32 | 0.24 | intron-variant | Pex2 | Mm_Celera | 3:5563417 | TTTTTGAAATGAGGA[C/T]TATCTGACAACACAG | 19302 |
rs33276808 | snp | A/C | 0.32 | 0.24 | intron-variant | Pex2 | Mm_Celera | 3:5563537 | AACAGGGCAAGCTGC[A/C]TGGTGACACCTCTTC | 19302 |
rs33276811 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pex2 | Mm_Celera | 3:5564851 | AATCTGCATTGGCTG[C/T]CATGTGCCCTTGACA | 19302 |
rs33277116 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pex2 | Mm_Celera | 3:5569665 | ATTGTAAACATGATA[C/T]CACTATTAGATGTGC | 19302 |
rs33277119 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pex2 | Mm_Celera | 3:5569764 | AAGATAAAATGGCAT[C/T]GGTAAAGAGTAAAGT | 19302 |
rs33277122 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Pex2 | Mm_Celera | 3:5570432 | GTCTCAAAATGTGAA[A/C]ATAGTGAAGAGGGCC | 19302 |
rs33277455 | snp | A/C | 0.391111 | 0.206368 | downstream-variant-500B | Pex2 | Mm_Celera | 3:5559689 | GAGAAAGGGGGTAAA[A/C]ATCAGACATATTCTA | 19302 |
rs33277458 | snp | C/T | 0.32 | 0.24 | downstream-variant-500B | Pex2 | Mm_Celera | 3:5559780 | GTGAATGGACACACG[C/T]GAGGACTCTACTTAT | 19302 |
rs33277461 | snp | A/G | 0.260355 | 0.249785 | downstream-variant-500B | Pex2 | Mm_Celera | 3:5559976 | ATCTCTGAATATTAA[A/G]AAATAGATATTATTT | 19302 |
rs33277644 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Pex2 | Mm_Celera | 3:5564854 | CTGCATTGGCTGCCA[G/T]GTGCCCTTGACATTC | 19302 |
rs33277646 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pex2 | Mm_Celera | 3:5564949 | CTACATGATAAGTAC[C/T]GATGCTATGACTATT | 19302 |
rs33277649 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Pex2 | Mm_Celera | 3:5565042 | TAATTATTTGATAAA[C/T]AGAAAAATGAACAGA | 19302 |
rs33277653 | snp | G/T | 0.124444 | 0.216185 | intron-variant, utr-variant-5-prime | Pex2 | Mm_Celera | 3:5565169 | ATAGAATGAATGGCA[G/T]TTGTGAGTATTGTGG | 19302 |
rs33277866 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pex2 | Mm_Celera | 3:5570814 | AACACCCCATTCGAA[C/T]ATATTTTGCCTCATT | 19302 |
rs33277869 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pex2 | Mm_Celera | 3:5570875 | TATTATTCAGGCAAA[A/G]AGGCATATAAAACTG | 19302 |
rs33278204 | snp | A/G | 0.32 | 0.24 | downstream-variant-500B | Pex2 | Mm_Celera | 3:5560149 | AAGGGCACTTGATAT[A/G]AATTCCTATATTATT | 19302 |
rs33278207 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime, downstream-variant-500B | Pex2 | Mm_Celera | 3:5560222 | TGTTTATTGCAAATA[C/T]CAGTACTGATCTCAG | 19302 |
rs33278209 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime, downstream-variant-500B | Pex2 | Mm_Celera | 3:5560313 | TGCCTTAAGCAGCTT[C/T]TACATTTTGAATGTA | 19302 |
rs33278211 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime | Pex2 | Mm_Celera | 3:5560507 | ACAATCATCCCAGAG[C/T]CTCAAAAATCTTTTA | 19302 |
rs33278212 | snp | A/T | 0.336735 | 0.234472 | utr-variant-3-prime | Pex2 | Mm_Celera | 3:5560555 | TTTTCTATGAAGAAG[A/T]ATTCTTAGTCATTCT | 19302 |
rs33278695 | snp | A/T | 0.32 | 0.24 | intron-variant | Pex2 | Mm_Celera | 3:5565228 | GAGACAGGACGGGTA[A/T]GCTATATAAAATAAG | 19302 |
rs33278698 | snp | A/G | 0.32 | 0.24 | intron-variant | Pex2 | Mm_Celera | 3:5565267 | GTACAGTGAGCTGCA[A/G]TATGTGATTCTCAAG | 19302 |
rs33278703 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | Pex2 | Mm_Celera | 3:5565548 | AGGGCTGGCAGCCCA[A/C]TGACTATTTAACAGG | 19302 |
rs33278844 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Pex2 | Mm_Celera | 3:5571747 | CTTAGGAATTCCATT[A/T]ATCAAAGTGGATGGA | 19302 |
rs33278847 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pex2 | Mm_Celera | 3:5571940 | CTAACAAATGGTACA[C/T]GCATCAGAAAGGGAC | 19302 |
rs33278850 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pex2 | Mm_Celera | 3:5572058 | TGAACAGTGCTAAAC[C/T]CCATCTAATTCTACT | 19302 |
rs33278853 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pex2 | Mm_Celera | 3:5572116 | ACTACTCTGTTGTTC[C/T]TCCCTCTATTACAAT | 19302 |
rs33279474 | snp | C/T | 0.124444 | 0.216185 | missense | Pex2 | Mm_Celera | 3:5561032 | CACTCTTTTCCACTG[C/T]TGCCTAGTGTACTGT | 19302 |
rs33279476 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Pex2 | Mm_Celera | 3:5561100 | AGACAATTTGGCTTT[C/T]AACTTCTGGATATTG | 19302 |
rs33279478 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Pex2 | Mm_Celera | 3:5561454 | TTTCTGAGTTTTACT[C/T]GGTGGCTGGTATATC | 19302 |
rs33279481 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pex2 | Mm_Celera | 3:5562125 | CATAGCTGTTTACTT[A/G]CTCTGAAAATATACT | 19302 |
rs33279488 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Pex2 | Mm_Celera | 3:5572555 | ACAGAATTTCTAACA[C/G]CTTTACTTAACCTCA | 19302 |
rs33279491 | snp | C/T | 0.32 | 0.24 | intron-variant | Pex2 | Mm_Celera | 3:5572868 | AGTGTTTTCTCAAAG[C/T]TTGAAAAGAGCAGAT | 19302 |
rs33279786 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Pex2 | Mm_Celera | 3:5565683 | CATTCCAGTGCTCTA[A/T]TATGGGAAATTTATG | 19302 |
rs33279789 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Pex2 | Mm_Celera | 3:5565755 | ATAAGATGGGGTAGA[C/G]AGTTTGGGTGCAGAT | 19302 |
rs33279791 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Pex2 | Mm_Celera | 3:5565819 | CTTTATCTGGTTAAA[C/T]ATTAAATGAAGAAGC | 19302 |
rs33279793 | snp | G/T | 0.497778 | 0.0332592 | intron-variant | Pex2 | Mm_Celera | 3:5565856 | TATAAACTTCTGGTG[G/T]CCCAAATCTTCTCAC | 19302 |
rs33280466 | snp | A/T | 0.32 | 0.24 | intron-variant | Pex2 | Mm_Celera | 3:5562254 | TACACAGAACATGGC[A/T]ACAGATGGTTAAATC | 19302 |
rs33280775 | snp | C/G/T | 0.32 | 0.24 | intron-variant | Pex2 | GRCm38.p3 | 3:5565898 | CTTTCTTTAAAACAA[C/G/T]AATCTTACTTACATT | 19302 |
rs33280778 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Pex2 | Mm_Celera | 3:5566014 | TTCTCAAACTGAAGA[G/T]CTTCCCAGAATCACT | 19302 |
rs33280780 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Pex2 | Mm_Celera | 3:5566043 | CTCCCAGGATCACAG[C/G]AAAGGATGGCTGACT | 19302 |
rs33280783 | snp | A/G | 0.32 | 0.24 | intron-variant | Pex2 | Mm_Celera | 3:5567959 | CTCTTCCTATCACCT[A/G]TGCATGGTTGTCCGG | 19302 |
rs33281846 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pex2 | Mm_Celera | 3:5567978 | ATGGTTGTCCGGTTA[C/T]TCGTTTCTAGCTGGT | 19302 |
rs33281849 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Pex2 | Mm_Celera | 3:5568035 | GTATAAACCTTTCAG[A/T]GACTCAGAATGCATC | 19302 |
rs33281851 | snp | C/G | 0.32 | 0.24 | intron-variant | Pex2 | Mm_Celera | 3:5568299 | TTCTATTAGCTAACA[C/G]AAGCCTACATGATTT | 19302 |
rs33281853 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Pex2 | Mm_Celera | 3:5568386 | TTTGATAGATGGCTT[A/T]CCTAGCCAAGAACAG | 19302 |
rs33282985 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Pex2 | Mm_Celera | 3:5568391 | TAGATGGCTTTCCTA[C/G]CCAAGAACAGATGAG | 19302 |
rs33282988 | snp | G/T | 0.32 | 0.24 | intron-variant | Pex2 | Mm_Celera | 3:5568597 | AGATGGGGGGCAATG[G/T]TTGGAAGCCAGTTAG | 19302 |
rs33282991 | snp | C/T | 0.32 | 0.24 | intron-variant | Pex2 | Mm_Celera | 3:5568768 | TCTTTCTAGAGAAAT[C/T]ATACTTGAGATCATG | 19302 |
rs33283824 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Pex2 | Mm_Celera | 3:5568793 | ATCATGTAGTAAAGA[A/G]GAATTTTTAATAACT | 19302 |
rs33861865 | snp | C/T | 0.375 | 0.216506 | utr-variant-5-prime, upstream-variant-2KB | Pex2 | Mm_Celera | 3:5576145 | CTCACTTCCGGAATC[C/T]GCGGGCTTCCGGAGC | 19302 |
rs45745370 | snp | C/T | | | upstream-variant-2KB | Pex2 | Mm_Celera | 3:5578053 | TTACTGCTGAAAATA[C/T]TTAAAATCAGGATAT | 19302 |
rs45848693 | snp | C/G | | | intron-variant | Pex2 | GRCm38.p3 | 3:5566220 | ATATCAAGCAGCTTT[C/G]GCATATCAAGTTGCA | 19302 |
rs45925371 | snp | A/G | | | upstream-variant-2KB | Pex2 | Mm_Celera | 3:5577605 | TGTGCTGGGAAGACA[A/G]CTGCATATTTTCTTG | 19302 |
rs46086425 | snp | C/T | | | intron-variant | Pex2 | GRCm38.p3 | 3:5566477 | TGTGGTGTCCTTGAC[C/T]TCTTTGGCTCCTTTA | 19302 |
rs46091849 | snp | A/G | | | intron-variant | Pex2 | Mm_Celera | 3:5566056 | AGCAAAGGATGGCTG[A/G]CTTCTACCTTTTCCT | 19302 |
rs46239318 | snp | A/C | | | intron-variant | Pex2 | Mm_Celera | 3:5566044 | TCCCAGGATCACAGC[A/C]AAGGATGGCTGACTT | 19302 |
rs46302895 | snp | A/G | | | upstream-variant-2KB | Pex2 | Mm_Celera | 3:5577207 | AGGGATGTGTCTAGA[A/G]ATGCACCAGTATACC | 19302 |
rs46501504 | snp | A/G | | | upstream-variant-2KB | Pex2 | Mm_Celera | 3:5578080 | ATATATTTATATAGT[A/G]TACTTCATTAATCTT | 19302 |
rs46581051 | snp | C/T | | | upstream-variant-2KB | Pex2 | Mm_Celera | 3:5577328 | AAGGGATACAAAATA[C/T]TCATCAATTTGATGC | 19302 |
rs46583243 | snp | C/T | | | upstream-variant-2KB | Pex2 | Mm_Celera | 3:5578194 | AAAACCTGAGCTGGG[C/T]TTTATTCCTGGGCCA | 19302 |
rs46712567 | snp | A/C | | | intron-variant | Pex2 | GRCm38.p3 | 3:5566855 | CTATAACCACCATTG[A/C]TAGGCACCTTCATTA | 19302 |
rs46909217 | snp | A/C | | | upstream-variant-2KB | Pex2 | Mm_Celera | 3:5578781 | AGTTAACACCTCAAA[A/C]CAACACTTATTTTTA | 19302 |
rs46920219 | snp | C/T | | | upstream-variant-2KB | Pex2 | Mm_Celera | 3:5577711 | GCTCAGGAATGAAGG[C/T]ACTTTCTGCCAAGCA | 19302 |
rs47523458 | snp | C/T | | | upstream-variant-2KB | Pex2 | Mm_Celera | 3:5578337 | GCATATCATATTTTG[C/T]ATTTGTAAATTCAAC | 19302 |