SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6154738 | snp | C/G | 0.207612 | 0.24638 | intron-variant | Trip12 | Mm_Celera | 1:84775914 | TAACTGGACTTATAG[C/G]ACAATATTTCAGTTA | 14897 |
rs6327838 | snp | A/T | 0.5 | 0 | intron-variant | Trip12 | GRCm38.p3 | 1:84764570 | tattagaattacacc[A/T]gacttctcccccaga | 14897 |
rs6357735 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Fbxo36, Trip12 | Mm_Celera | 1:84844679 | GACTagaaaaatggc[C/T]tgctcttgcagaggt | 14897 |
rs6397722 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Fbxo36, Trip12 | Mm_Celera | 1:84840845 | AAAGTAAGTTTAAAA[C/T]CTTGTGTTTATTTGA | 14897 |
rs13460471 | snp | G/T | 0.444444 | 0.157135 | missense | Trip12 | GRCm38.p3 | 1:84732055 | CAGAGAGCTGACTTG[G/T]GTCTCTGGAGGGGTG | 14897 |
rs30246554 | snp | G/T | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Trip12 | Mm_Celera | 1:84833385 | TGTGATCCACATAGT[G/T]AGTTCCAGGACAATC | 14897 |
rs30246555 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trip12 | Mm_Celera | 1:84833233 | ATTCTCAGTAACCAT[A/G]TGGCAGCACACACAG | 14897 |
rs30246556 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Trip12 | Mm_Celera | 1:84833197 | AGAACACTGGCTCTT[C/G]TTCCAGAGGTCCTGA | 14897 |
rs30246557 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Trip12 | Mm_Celera | 1:84833086 | AACTCAGGGTCTGGC[A/G]CCTCAATGCTAGAAA | 14897 |
rs30246558 | snp | C/T | 0.32 | 0.24 | intron-variant | Trip12 | Mm_Celera | 1:84829931 | GAGTCTTGGACTAGG[C/T]ATAGTTCAGCGATTA | 14897 |
rs30246559 | snp | G/T | 0.21875 | 0.248039 | intron-variant | Trip12 | Mm_Celera | 1:84829825 | TGTTCTTAACGGCTG[G/T]ACAGTCTCTTCAGGC | 14897 |
rs30246560 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Trip12 | GRCm38.p3 | 1:84829611 | TTCAGGCTGGGCACA[A/G]AAATAGAACCAAGGA | 14897 |
rs30246561 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Trip12 | GRCm38.p3 | 1:84829588 | GCCACACTCAGAAAG[G/T]TTTTTATTTCAGGCT | 14897 |
rs30246562 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trip12 | Mm_Celera | 1:84829474 | GACCTTGAAAAGCCT[A/G]AGAGCTGGTGTTATA | 14897 |
rs30246563 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trip12 | GRCm38.p3 | 1:84828888 | GTTATACCTGTATTA[A/G]GTGGCTCACACCTGC | 14897 |
rs30246564 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Trip12 | GRCm38.p3 | 1:84786961 | TCCATTTATTTTTAG[G/T]TTTAAATATGCCAAT | 14897 |
rs30246565 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Trip12 | Mm_Celera | 1:84786406 | TCAAGAATTTAATCA[C/T]GTTAACTTTACACTA | 14897 |
rs30246566 | snp | A/T | 0.32 | 0.24 | intron-variant | Trip12 | Mm_Celera | 1:84786325 | CTCAGCCCAAACCTT[A/T]CCTTACAGTAGCAGT | 14897 |
rs30246567 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Trip12 | Mm_Celera | 1:84786312 | ATCTGAACAATCACT[A/C]AGCCCAAACCTTTCC | 14897 |
rs30246568 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trip12 | Mm_Celera | 1:84785826 | GACAAGCAACCATCT[A/G]TACAGCCACAGTCTG | 14897 |
rs30246569 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Trip12 | Mm_Celera | 1:84785363 | CCCAGCCACACCTGC[C/G]TGAGTGTACTCTTTA | 14897 |
rs30246570 | snp | A/C/G | 0.142012 | 0.225474 | intron-variant | Trip12 | GRCm38.p3 | 1:84785313 | GTACACCAAGATGTA[A/C/G]CCTGCCTCTTCCTCC | 14897 |
rs30246571 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trip12 | Mm_Celera | 1:84785292 | TTTCTGTCAGAAACT[C/T]GCAATGTACACCAAG | 14897 |
rs30246572 | snp | A/G | 0.32 | 0.24 | intron-variant | Trip12 | Mm_Celera | 1:84784750 | TTCAATTAAAAACCT[A/G]GCCCAAAAGCTCTGT | 14897 |
rs30246573 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trip12 | Mm_Celera | 1:84784590 | ATCAAAGATCAATTA[C/T]GAGCTCCCAGAATCT | 14897 |
rs30247304 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Trip12 | GRCm38.p3 | 1:84828799 | CAAAGCTCTGGATTC[C/T]ATTCTCTCAAAAAAA | 14897 |
rs30247305 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Trip12 | GRCm38.p3 | 1:84828409 | CAGTCCTTTATTCAG[C/T]CACAGATGTCCTTTT | 14897 |
rs30247306 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trip12 | GRCm38.p3 | 1:84827559 | AATTATCTTTATTGC[C/T]ACTTCATAACTGTAA | 14897 |
rs30247307 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Trip12 | GRCm38.p3 | 1:84827151 | ATAGTATGAAACCAC[A/C]TAAGAGTCAGACCTG | 14897 |
rs30247308 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Trip12 | GRCm38.p3 | 1:84827123 | CAAACTTATGAAAAT[A/G]GAGCAGAGTATTATA | 14897 |
rs30247309 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Trip12 | GRCm38.p3 | 1:84826572 | AGAGAAATATGGGAG[G/T]TGAGTTCAAGATGAG | 14897 |
rs30247310 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Trip12 | Mm_Celera | 1:84826400 | AGGACTTTGGAGTGA[A/G]CTTGCAGCCCAACAG | 14897 |
rs30247311 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Trip12 | Mm_Celera | 1:84826369 | CCAGAAGGGAGAGAC[A/G]AGCAAACAGATTTCT | 14897 |
rs30247312 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Trip12 | Mm_Celera | 1:84826328 | CAAGCCAAATCAGGC[C/T]CAGTGTGTTAACCCA | 14897 |
rs30247313 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Trip12 | Mm_Celera | 1:84826306 | ACTGATAGCACCTTT[A/G]CTATTTCAAGCCAAA | 14897 |
rs30247444 | snp | A/C | 0.32 | 0.24 | intron-variant | Trip12 | Mm_Celera | 1:84783723 | TTGAGGAGTTTCTTT[A/C]TTAGTGAAAGCTAAA | 14897 |
rs30247445 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trip12 | Mm_Celera | 1:84783370 | TGCCCATACTTTATG[A/G]CAAACTACCTAAATC | 14897 |
rs30247446 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trip12 | Mm_Celera | 1:84783278 | TTTAAAATACAGCCT[C/T]ATTTACAAACATAGA | 14897 |
rs30247447 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Trip12 | Mm_Celera | 1:84783087 | TAAATAAAAAATTGT[A/T]ATAGAAAATCACTAC | 14897 |
rs30247448 | snp | A/G | 0.32 | 0.24 | intron-variant | Trip12 | GRCm38.p3 | 1:84782609 | CTCTGAAAGTAGTAC[A/G]TGTATGGACTGCTTG | 14897 |
rs30247449 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Trip12 | Mm_Celera | 1:84782561 | CAATATATAAAAACC[G/T]TAAATGGAAAATTTA | 14897 |
rs30247450 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Trip12 | Mm_Celera | 1:84781937 | CAATTAACTATTAAG[A/G]AAAAGATTTTTAAAA | 14897 |
rs30247451 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Trip12 | Mm_Celera | 1:84781774 | ATTCCATTCCTGTCA[C/G]TCAATTTGAGAATTG | 14897 |
rs30247452 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trip12 | Mm_Celera | 1:84781726 | GTGTTGCTGTAATTA[C/T]TGTAACTATCAACTT | 14897 |
rs30247453 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trip12 | Mm_Celera | 1:84781371 | GAATGACAATAAAGC[A/G]CACTATATTCCCTTG | 14897 |
rs30248104 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Trip12 | GRCm38.p3 | 1:84825450 | TGAAACCAACAGCAA[C/T]TGACAATTAGCAAGC | 14897 |
rs30248105 | snp | A/G | 0.5 | 0 | intron-variant | Trip12 | GRCm38.p3 | 1:84824793 | AGAAACCAAAGGGAC[A/G]GGCTGAAAAGAATGT | 14897 |
rs30248106 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Trip12 | Mm_Celera | 1:84823372 | TACACTATGCTATTT[A/T]AAAAATGCTAGGAAA | 14897 |
rs30248107 | snp | A/G | 0.188366 | 0.242283 | intron-variant | Trip12 | Mm_Celera | 1:84823360 | AAACTACTGTACTAC[A/G]CTATGCTATTTTAAA | 14897 |
rs30248108 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Trip12 | Mm_Celera | 1:84823196 | AACCACATGGTGGCT[C/T]ACAGCTATCTATAAT | 14897 |
rs30248109 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trip12 | Mm_Celera | 1:84822866 | TTCTTGCCTACTGTG[C/T]AGAAAGCTCTAGACT | 14897 |
rs30248110 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Trip12 | GRCm38.p3 | 1:84822447 | ATATATTGAGGAATC[A/G]AGATGGTAGTTTAAC | 14897 |
rs30248111 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trip12 | Mm_Celera | 1:84822386 | CTTCTTACCAATTGG[A/G]CTTGTTTGCTTGAGA | 14897 |
rs30248112 | snp | A/T | 0.459184 | 0.136902 | intron-variant | Trip12 | GRCm38.p3 | 1:84822247 | ACAAAAAGGAAACTT[A/T]AAAAAAAATGACCTA | 14897 |
rs30248113 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trip12 | Mm_Celera | 1:84822173 | GGTGGTGGTACACAA[A/G]TCTTTAATCCCAGGA | 14897 |
rs30248294 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trip12 | Mm_Celera | 1:84781219 | TATTTTACAGCCAGA[A/G]GAATTTGTACTATCC | 14897 |
rs30248295 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trip12 | Mm_Celera | 1:84781199 | CCAGCACATTTTCCC[C/T]GAAGTATTTTACAGC | 14897 |
rs30248296 | snp | C/G | 0.32 | 0.24 | intron-variant | Trip12 | Mm_Celera | 1:84781057 | TCTTCTAACCAACTA[C/G]AGACATCACTTGGAG | 14897 |
rs30248297 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Trip12 | GRCm38.p3 | 1:84781038 | TTCACTGTTCTGAAA[A/G]AAGTCTTCTAACCAA | 14897 |
rs30248298 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Trip12 | Mm_Celera | 1:84780337 | TGTTTTTTACTGTGC[A/T]TTCCATCATCTGGTA | 14897 |
rs30248299 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trip12 | Mm_Celera | 1:84780278 | AAGGGGCAATAGGAA[A/G]ATCTATGTCATAAAA | 14897 |
rs30248300 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trip12 | Mm_Celera | 1:84780228 | GATTTTCACTTGCCA[A/G]AAATTGCTAAGTAGC | 14897 |
rs30248301 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Trip12 | Mm_Celera | 1:84779387 | AAAGTGAACTTTTTG[C/G]CAGCCCTTTTATGAG | 14897 |
rs30248302 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trip12 | Mm_Celera | 1:84779320 | AGGTACTCTGCTTTT[A/G]CAAAAGGGTAAGTTG | 14897 |
rs30248303 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trip12 | Mm_Celera | 1:84779208 | ATCCTCATGGACATA[C/T]AAAACAGACCAAAAG | 14897 |
rs30248314 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Trip12 | Mm_Celera | 1:84754036 | CCCTGGGGTAAACGA[G/T]ATGTATGCATTTTAT | 14897 |
rs30248315 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Trip12 | Mm_Celera | 1:84753713 | AACATAAAAAACATA[G/T]AATAAAAGCACTAGT | 14897 |
rs30248316 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Trip12 | Mm_Celera | 1:84753346 | TTTGAGGTTTTACTG[A/T]TTTAATTTTAGGATC | 14897 |
rs30248317 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trip12 | GRCm38.p3 | 1:84753336 | ACAATAGTTCTTTGA[A/G]GTTTTACTGTTTTAA | 14897 |
rs30248318 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Trip12 | Mm_Celera | 1:84753298 | TCAAATACCCAACTC[A/C]AGCAATCTATCCAGC | 14897 |
rs30248319 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Trip12 | Mm_Celera | 1:84752100 | GACTTAATATGGACT[A/C]TCGTGGACAGTCATA | 14897 |
rs30248320 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Trip12 | Mm_Celera | 1:84751502 | CTCAATACAATCATG[A/T]TGAGACCTTTCATCC | 14897 |
rs30248321 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Trip12 | Mm_Celera | 1:84751395 | TTTATAGGGTTGAAC[A/T]CACAGGCAAATCCTC | 14897 |
rs30248322 | snp | C/T | 0.32 | 0.24 | intron-variant | Trip12 | Mm_Celera | 1:84751260 | AGTAGCTACCCTCAG[C/T]TACAAATCTTCAAAT | 14897 |
rs30248323 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Trip12 | Mm_Celera | 1:84751135 | TAGAGGAATCGGTTT[A/T]CACAGGTACTCTGTA | 14897 |
rs30248784 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trip12 | Mm_Celera | 1:84821841 | CATATGCCAAACCTT[C/T]CCTCAAGTATCAATG | 14897 |
rs30248785 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trip12 | Mm_Celera | 1:84821223 | CCCACTCCAAAAAAC[A/G]TTAAAAACTAGAAAG | 14897 |
rs30248786 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trip12 | Mm_Celera | 1:84821135 | ACATTTTAAATTAGA[C/T]AGTGGCCTTTAATCT | 14897 |
rs30248787 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trip12 | Mm_Celera | 1:84820634 | TAAACCTTACTCACC[C/T]TTAAGCTCAGCACTG | 14897 |
rs30248788 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Trip12 | Mm_Celera | 1:84820586 | TAAGCCTTTTTTTTT[G/T]TGTGCTTCCATAGCA | 14897 |
rs30248789 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Trip12 | Mm_Celera | 1:84820110 | ATGGATTCACCAAAG[A/T]TTTTCCCCAAGGCTA | 14897 |
rs30248790 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Trip12 | GRCm38.p3 | 1:84819468 | TTAACCACTCCAGCC[C/T]AAGTCTTAATTTTTA | 14897 |
rs30248791 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trip12 | Mm_Celera | 1:84819466 | TCTTAACCACTCCAG[C/T]CTAAGTCTTAATTTT | 14897 |
rs30248792 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trip12 | Mm_Celera | 1:84817647 | ATACAGACCTTTTTA[C/T]TCTGGGTATTTTAGT | 14897 |
rs30248793 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Trip12 | Mm_Celera | 1:84816997 | GCCAAGTCAGAGTAG[A/C]TGTGCGTAAGAAGGT | 14897 |
rs30248904 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trip12 | Mm_Celera | 1:84778917 | CAGTTATAGTCATTA[C/T]ACCAATGTCCTATAA | 14897 |
rs30248905 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Trip12 | Mm_Celera | 1:84778902 | TTGGAATTTTAAATT[C/T]AGTTATAGTCATTAT | 14897 |
rs30248906 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trip12 | Mm_Celera | 1:84778857 | TAGCAAGGTTTCACT[C/T]CTATTCTCTGAAGTA | 14897 |
rs30248907 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trip12 | Mm_Celera | 1:84778810 | CATCACTTAAGTGTT[C/T]ATGCCAGCTAGGAAT | 14897 |
rs30248908 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Trip12 | GRCm38.p3 | 1:84778775 | AGATCCTTCATGCAC[A/T]GGAAAAAAAATTAAG | 14897 |
rs30248909 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Trip12 | Mm_Celera | 1:84778559 | TGCCAATGAGCCAGC[A/C]ACCAATTCTACATTT | 14897 |
rs30248910 | snp | C/T | 0.32 | 0.24 | intron-variant | Trip12 | GRCm38.p3 | 1:84778085 | AGTAGTATGGTAAAT[C/T]GCTAAGTATATGCTT | 14897 |
rs30248911 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trip12 | GRCm38.p3 | 1:84777914 | AGTGCAAAGAACTGC[C/T]GTCAAGTATGAAAAA | 14897 |
rs30248912 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Trip12 | Mm_Celera | 1:84777902 | AACTAACACACAAGT[C/G]CAAAGAACTGCCGTC | 14897 |
rs30248913 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trip12 | GRCm38.p3 | 1:84777225 | TTAAACAGTAAAAAT[A/G]AAGACACAGACAGGT | 14897 |
rs30249014 | snp | C/T | 0.32 | 0.24 | intron-variant | Trip12 | Mm_Celera | 1:84750778 | GCAAATTCAGCTTCA[C/T]TCTCAAAATGGACTA | 14897 |
rs30249015 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trip12 | Mm_Celera | 1:84750627 | CGGTGCTGAGTTCAA[C/T]GCCTGGGAGAACCAA | 14897 |
rs30249016 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Trip12 | Mm_Celera | 1:84749940 | AAAATTAGAATAAGG[C/T]TTTTTTAGAAAGCCA | 14897 |
rs30249017 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trip12 | Mm_Celera | 1:84749146 | TAGTACCCATGAGCA[C/T]TATCAACTTACTGGA | 14897 |
rs30249018 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trip12 | Mm_Celera | 1:84749109 | TGGGACACAAATACA[C/T]CCACTTGCTAGCTCT | 14897 |