SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6192787 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Trim33 | Mm_Celera | 3:103317446 | TCTTTAGTTTTTATT[C/T]ATTACTTCCTAGTCT | 94093 |
rs6212566 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Trim33 | Mm_Celera | 3:103318795 | TCATGTGTCTTGTCT[C/T]TTCTTTGTTCACACG | 94093 |
rs6213645 | snp | A/C | 0.5 | 0 | intron-variant | Trim33 | GRCm38.p3 | 3:103319021 | TTTTAAAATCATGCC[A/C]TGATCTATAACCAAT | 94093 |
rs6348511 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim33 | Mm_Celera | 3:103305242 | GTCTTCTGTCCTTTA[C/T]TTCTTTAGTAATCAA | 94093 |
rs6349646 | snp | C/T | 0.5 | 0 | intron-variant | Trim33 | Mm_Celera | 3:103305443 | CTTACTGCATTATCA[C/T]TATGAAGTAATTCCT | 94093 |
rs6350012 | snp | C/T | 0.5 | 0 | intron-variant | Trim33 | Mm_Celera | 3:103305466 | TAATTCCTTTATGTT[C/T]TGTGTGTATNAATTT | 94093 |
rs6350026 | snp | A/G | 0.5 | 0 | intron-variant | Trim33 | Mm_Celera | 3:103305476 | ATGTTNTGTGTGTAT[A/G]AATTTTGCCTGTTGT | 94093 |
rs29975407 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trim33 | Mm_Celera | 3:103333731 | TTTTCTTCTTTTGAA[A/G]AAAGGGACTTGAAGT | 94093 |
rs30053748 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Trim33 | Mm_Celera | 3:103301809 | GCAACAGTTGGAGAC[A/T]GTCACACTAGGCATA | 94093 |
rs30358314 | snp | A/G | 0.375 | 0.216506 | intron-variant | Trim33 | GRCm38.p3 | 3:103328435 | AAGGAAAGAAAGAAG[A/G]AAAGAAAGAAAAAAG | 94093 |
rs30409445 | snp | A/G/T | 0.444444 | 0.157135 | intron-variant | Trim33 | GRCm38.p3 | 3:103336436 | TTTTTTTTTGTTTTT[A/G/T]TTTTTGTTTTTTTGA | 94093 |
rs30692751 | snp | C/T | 0.375 | 0.216506 | intron-variant | Trim33 | Mm_Celera | 3:103296414 | TACTGAGGAAAGAAC[C/T]ACAATATCAGACAGA | 94093 |
rs31147941 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trim33 | Mm_Celera | 3:103333760 | GTGTAGTCTGGTCTA[A/G]AGTCCACTGTGTAGC | 94093 |
rs31194806 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Trim33 | Mm_Celera | 3:103301810 | CAACAGTTGGAGACT[C/G]TCACACTAGGCATAG | 94093 |
rs31280643 | snp | A/G | 0.5 | 0 | intron-variant | Trim33 | GRCm38.p3 | 3:103295739 | AGAACAGCTTTTTTA[A/G]CTGCCAGTAAGCTCA | 94093 |
rs31358934 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim33 | Mm_Celera | 3:103282920 | CAGATATATCAAAAA[C/T]TGAATTTTGGCTGAT | 94093 |
rs31526782 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trim33 | Mm_Celera | 3:103328351 | TTTAAAGAAAGAAAG[A/G]AAGGAAGGAAGGAAG | 94093 |
rs31571722 | snp | A/G | 0.465374 | 0.126941 | utr-variant-3-prime | Trim33 | GRCm38.p3 | 3:103358313 | ATGCACACCTGTAAT[A/G]TGAGGTGTGCGCAAT | 94093 |
rs31623653 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Trim33 | GRCm38.p3 | 3:103318407 | TACAGCTGCCAGTGT[C/T]TCCAGTTACAGGGGA | 94093 |
rs31668253 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trim33 | Mm_Celera | 3:103333888 | GTGCTGAGAGTCTTA[A/G]ACTGTACTATGTGTC | 94093 |
rs31737097 | snp | A/G | 0.5 | 0 | intron-variant | Trim33 | GRCm38.p3 | 3:103330421 | CTCTTTAAACTTACA[A/G]TATGGATTAAGATAC | 94093 |
rs33498435 | snp | C/T | 0.486111 | 0.0821678 | synonymous-codon, nc-transcript-variant | Trim33 | Mm_Celera | 3:103326135 | ACAGCAGCAGAATGA[C/T]ATCACAGGCCTCTCC | 94093 |
rs33498438 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Trim33 | Mm_Celera | 3:103326289 | CTAATGGACGAATTA[A/T]TTACAAGTGTAGAAT | 94093 |
rs33498441 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Trim33 | Mm_Celera | 3:103326525 | TTATCTTTCTGTTGT[C/T]CCCATTTACTTTTGA | 94093 |
rs33499044 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Trim33 | Mm_Celera | 3:103327690 | AGTAGAATGAAATGA[A/G]ACAGTATGACTCAGA | 94093 |
rs33499047 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Trim33 | Mm_Celera | 3:103328002 | AATATTACCTCAAAG[A/G]AAATGACTATAAAAA | 94093 |
rs33499052 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Trim33 | Mm_Celera | 3:103330939 | TGTCTCAAAAGCCAA[C/T]TATATAGGGTGGAGA | 94093 |
rs33499055 | snp | C/G | 0.32 | 0.24 | intron-variant | Trim33 | GRCm38.p3 | 3:103308609 | ATGGTGTTTTCTAGA[C/G]TTGTGTGTTATACAC | 94093 |
rs33499057 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim33 | Mm_Celera | 3:103308648 | ACACTAAATTTAGTC[C/T]TTGGATTATATTTGT | 94093 |
rs33499059 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Trim33 | Mm_Celera | 3:103309250 | TTTTCTTCCTCTTGC[G/T]TGAAGAGCTTGATTT | 94093 |
rs33499061 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Trim33 | Mm_Celera | 3:103309344 | GTTTTGGGTGAAGAA[A/T]TCATTCATTGTCTTC | 94093 |
rs33500005 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Trim33 | Mm_Celera | 3:103331435 | TACATAAAAACGAGT[A/G]AAAAATGAAGACTCG | 94093 |
rs33500008 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Trim33 | Mm_Celera | 3:103331470 | AACTGTTCTCTTGCA[C/T]ATGAGAGGCCCCCAC | 94093 |
rs33500011 | snp | C/T | 0.375 | 0.216506 | intron-variant | Trim33 | Mm_Celera | 3:103332064 | AGCACATTCCAAAGG[C/T]AGGCCTCAGTCAAAT | 94093 |
rs33500394 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Trim33 | GRCm38.p3 | 3:103309428 | CTGTTGTGCTGTTGC[A/G]TCTGCGTCTGAGTGC | 94093 |
rs33500397 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim33 | Mm_Celera | 3:103310074 | TAGCATTTCTTTTAG[A/G]ACTGTCAGCTAATTC | 94093 |
rs33500399 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Trim33 | Mm_Celera | 3:103311517 | CAAAGAACATAGGTA[C/T]AGAAGTCATAATTCT | 94093 |
rs33500401 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Trim33 | Mm_Celera | 3:103312506 | TTTTATGCTGGGCAC[C/T]TTTCTCAGTACCAAG | 94093 |
rs33500884 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Trim33 | Mm_Celera | 3:103332538 | AATAATATGTGTCTT[C/T]CATGTCTTTTGACAT | 94093 |
rs33500887 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim33 | Mm_Celera | 3:103332622 | GATTCTGTTATTTTC[C/T]CTTAGTAGAGTTGGA | 94093 |
rs33500889 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim33 | Mm_Celera | 3:103333070 | TTATTTGAAACCACT[A/G]ACTTCTGTGATTCTT | 94093 |
rs33500892 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim33 | Mm_Celera | 3:103333144 | TTAAGGGAATGGTAA[C/T]AGTGCTGAGAGTATT | 94093 |
rs33501414 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Trim33 | Mm_Celera | 3:103312546 | GGTTCATGAAATATT[A/C]AGGTGCTGGTGCTAT | 94093 |
rs33501417 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim33 | Mm_Celera | 3:103312881 | GACTAACATGTGGAG[A/G]ACTTTACCTTTAAGG | 94093 |
rs33501420 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim33 | Mm_Celera | 3:103313406 | TTGGTGAAAAGCATA[C/T]GAAAAGAGAGATGGT | 94093 |
rs33501423 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Trim33 | Mm_Celera | 3:103314015 | TTATTCTCAGTGTGA[A/T]CAGCTCTCTGACACC | 94093 |
rs33501755 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim33 | Mm_Celera | 3:103334487 | CCCTGCTGCTATAGC[C/T]TAGACAGTAAGTATT | 94093 |
rs33501758 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Trim33 | Mm_Celera | 3:103335606 | GGTGCTAAAGTGAAA[A/C]TCCCTGAAAAAAATT | 94093 |
rs33501761 | snp | G/T | 0.32 | 0.24 | intron-variant | Trim33 | GRCm38.p3 | 3:103335662 | TAGGAGGTAGTAAAT[G/T]GAAGCCAGAATGCTT | 94093 |
rs33502223 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Trim33 | GRCm38.p3 | 3:103288181 | ACAAATGCCCTACTG[C/T]TGAGCTACACCACAG | 94093 |
rs33502316 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim33 | Mm_Celera | 3:103314046 | AAGTAGATGTTCTTT[A/G]ATTCACTTATAACAC | 94093 |
rs33502319 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim33 | Mm_Celera | 3:103314695 | AAAGTATTTAAAAAG[C/T]TCTGTCTCACCAGAT | 94093 |
rs33502322 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim33 | Mm_Celera | 3:103315374 | TAGGATACTCTAGTG[A/G]AATTTTCTTTCTACA | 94093 |
rs33502524 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Trim33 | Mm_Celera | 3:103336070 | CAGCACCCTCATGGT[A/G]GCTAACCACTGCCTA | 94093 |
rs33502527 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim33 | Mm_Celera | 3:103336285 | ATTCTGTAGTAGAGC[C/T]TACAAATGGATGCTT | 94093 |
rs33502530 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Trim33 | Mm_Celera | 3:103337118 | AAAAGGAATTAAAGT[G/T]TGCTGTTAGTGTATG | 94093 |
rs33502533 | snp | A/G | 0.32 | 0.24 | synonymous-codon, downstream-variant-500B | Trim33 | Mm_Celera | 3:103337512 | CCCAGGACCCTCTGC[A/G]TTATCACCTGGATCT | 94093 |
rs33502936 | snp | G/T | 0.142012 | 0.225474 | utr-variant-3-prime | Trim33 | Mm_Celera | 3:103356283 | AAAAAATAGAAAAAC[G/T]TAATTCTTATTCAAA | 94093 |
rs33502939 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Trim33 | Mm_Celera | 3:103356576 | TCTCGGCGCTTGACT[C/T]TCCTGCTTGACTGAG | 94093 |
rs33502942 | snp | A/G | 0.48 | 0.0979796 | utr-variant-3-prime | Trim33 | GRCm38.p3 | 3:103357475 | GTGCCCTCAAAACGT[A/G]CAAGTGGATACACCA | 94093 |
rs33503005 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim33 | Mm_Celera | 3:103288477 | TCCCTATAACCTAGA[A/G]AACACAATAATGACT | 94093 |
rs33503008 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Trim33 | GRCm38.p3 | 3:103289691 | TGGAGTGCTAATATC[C/T]AAACTATACAACATA | 94093 |
rs33503010 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim33 | Mm_Celera | 3:103289978 | TATGTAATAAACCTT[A/G]AGCCTGTTGAACCTT | 94093 |
rs33503013 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Trim33 | Mm_Celera | 3:103289998 | TGTTGAACCTTGCTG[A/T]GATGATAACACTCAA | 94093 |
rs33503185 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Trim33 | GRCm38.p3 | 3:103315730 | CCTGCCTTTCTTCAG[C/G]CATCATTAAAGTATG | 94093 |
rs33503188 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim33 | Mm_Celera | 3:103316882 | TGTTGAGGTGGCGGC[A/G]TTACTTCTTTCAAGT | 94093 |
rs33503386 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Trim33 | Mm_Celera | 3:103338016 | CTCACTGAAGTGATA[G/T]GATACTACTCAACAT | 94093 |
rs33503389 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Trim33 | Mm_Celera | 3:103338824 | CATGGGTTTTTCCAT[C/G]AGGTATTTTATTAAC | 94093 |
rs33503392 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Trim33 | Mm_Celera | 3:103340661 | CAGTGGAAACTTGGC[C/T]CTGAGTAGCTATACT | 94093 |
rs33503735 | snp | G/T | 0.231111 | 0.249285 | utr-variant-3-prime | Trim33 | Mm_Celera | 3:103357523 | ATTATCTGCTGAAGG[G/T]GTTTAAGATTTTTAA | 94093 |
rs33503738 | snp | A/G | 0.48 | 0.0979796 | utr-variant-3-prime | Trim33 | GRCm38.p3 | 3:103357621 | TGATAAAGCAATAAC[A/G]CTGCTTCGAGTCTGT | 94093 |
rs33503741 | snp | A/T | 0.244898 | 0.249948 | utr-variant-3-prime | Trim33 | GRCm38.p3 | 3:103358126 | TTTTCTAGCAAGTGT[A/T]ATTTAAAACTGAAAA | 94093 |
rs33504006 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Trim33 | Mm_Celera | 3:103290773 | AGGCCACAGAGGTAG[A/G]TTGATAAAATCATAC | 94093 |
rs33504009 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Trim33 | GRCm38.p3 | 3:103291034 | CTTTGAAGTTTAAGC[C/T]CTTTAAGTGCTTACG | 94093 |
rs33504012 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Trim33 | Mm_Celera | 3:103299931 | CATGTATGCTGCCTT[A/C]ATGTGAGTTACCTAA | 94093 |
rs33504315 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim33 | Mm_Celera | 3:103341242 | GTAGTATGTTGCGAT[C/T]AAATTGCTGGGTGGA | 94093 |
rs33504318 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Trim33 | Mm_Celera | 3:103341413 | AATTGCTTAACTTAA[A/G]TGTTTTGTGCCATGA | 94093 |
rs33504321 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim33 | Mm_Celera | 3:103341730 | GTATGGTAAGCTCCC[A/G]CCAGGATTTGATGGG | 94093 |
rs33504327 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Trim33 | Mm_Celera | 3:103320592 | ACATTTGAATATTCT[C/T]TGATCCTGTTGAAAT | 94093 |
rs33504330 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Trim33 | Mm_Celera | 3:103320911 | CCAAGGGCTGTGGAC[C/G]TTAGTATTAAATCTA | 94093 |
rs33504333 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Trim33 | Mm_Celera | 3:103321006 | GTAAAGCTACATTGG[C/T]ATCTTTATTTGATAG | 94093 |
rs33504584 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Trim33 | Mm_Celera | 3:103358195 | CAAAATGATTTTTAA[A/G]TGTCACAATGCTCCA | 94093 |
rs33504589 | snp | G/T | 0.231111 | 0.249285 | downstream-variant-500B | Trim33 | Mm_Celera | 3:103358776 | AAGTTTTCAAATGAA[G/T]TTCCTTTCTTTTTGA | 94093 |
rs33504592 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B | Trim33 | Mm_Celera | 3:103358861 | AATACAAGCCCTTGC[A/G]TTGACAGTGTTTTCA | 94093 |
rs33504805 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim33 | Mm_Celera | 3:103300567 | TGCTTTTATTGGTGT[A/G]TAGCAAATTATAGAA | 94093 |
rs33504808 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Trim33 | Mm_Celera | 3:103300588 | AATTATAGAAACTTT[A/T]GGCTGAATGTGGTGA | 94093 |
rs33504811 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Trim33 | Mm_Celera | 3:103302757 | TGTTTTCTTAATTAC[A/C]TAACACTTCATTTTT | 94093 |
rs33504884 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Trim33 | Mm_Celera | 3:103346313 | TTGTTATTTGATGTG[G/T]AATTGGGAAAGTTTG | 94093 |
rs33504887 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Trim33 | Mm_Celera | 3:103346550 | GTAATAGAAAAATTC[A/G]TGAAAGAATTGGAAA | 94093 |
rs33504890 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Trim33 | Mm_Celera | 3:103346588 | TAACCTAAAGACTTG[C/T]ACTAAGGGCCTTCTT | 94093 |
rs33504893 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim33 | Mm_Celera | 3:103347115 | AATACCAGACAAATA[C/T]ATCTTTCCTTAGTAT | 94093 |
rs33504904 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim33 | Mm_Celera | 3:103342522 | ATCTCAAGGCCACAA[C/T]GGAACCTTAACTATT | 94093 |
rs33504907 | snp | C/G | 0.32 | 0.24 | intron-variant | Trim33 | Mm_Celera | 3:103344004 | AAGGCTTATGGAACT[C/G]GTTTTGATTGGAAAA | 94093 |
rs33504910 | snp | C/T | 0.48 | 0.0979796 | synonymous-codon | Trim33 | GRCm38.p3 | 3:103344611 | GGTCTTTCATCTTAC[C/T]TGTCATGTTCCAACA | 94093 |
rs33504913 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Trim33 | Mm_Celera | 3:103345441 | ATATAAACTATAAAA[C/T]TTCTAGAATTAGAAC | 94093 |
rs33505376 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim33 | Mm_Celera | 3:103321310 | TGTATCTTATACAGG[C/T]TTAAAAAAAAATAGA | 94093 |
rs33505378 | snp | A/T | 0.32 | 0.24 | intron-variant | Trim33 | Mm_Celera | 3:103321728 | GAATGCATCCAAATT[A/T]AACTTATTTTCTTAC | 94093 |
rs33505380 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Trim33 | Mm_Celera | 3:103322854 | TTACAATTTTTGACA[C/T]GTATAACTGGCACAC | 94093 |
rs33505383 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Trim33 | Mm_Celera | 3:103323482 | TCTCTTTCCAGTGTG[C/T]TTTATGACTTCTGTT | 94093 |
rs33505485 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B | Trim33 | Mm_Celera | 3:103358948 | GTGATCAGTGTTCTT[C/T]AAGAAGGGAGAGATG | 94093 |