SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6312609 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Trim80 | GRCm38.p3 | 11:115439158 | AAAGGAACTCCAggg[A/G]ctggtgagatggctc | 432613 |
rs6313152 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | Trim80 | Mm_Celera | 11:115439278 | tctgactccctcttc[G/T]ggngtgtctgaagac | 432613 |
rs6313153 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | Trim80 | Mm_Celera | 11:115439281 | gactccctcttcngg[A/T]gtgtctgaagacagc | 432613 |
rs6314730 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Trim80 | Mm_Celera | 11:115439586 | ATGGTGACTCACCAG[C/T]TTCCCAATCCCTGAC | 432613 |
rs27031534 | snp | C/T | 0.165289 | 0.235211 | downstream-variant-500B, upstream-variant-2KB | Trim80, Mir3968 | Mm_Celera | 11:115448674 | CTTGAGTCAAGCCGA[C/T]TTCTCTCTCCAGGTG | 432613 |
rs27031535 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Trim80 | Mm_Celera | 11:115447160 | AGTTCCCAAGGCTTC[A/G]GAGATACTGAGAGTC | 432613 |
rs27031536 | snp | C/G | 0.5 | 0 | missense | Trim80 | Mm_Celera | 11:115446791 | ATGAGGTGCTGCCCG[C/G]AACTGTGGAGAGAAA | 432613 |
rs27031537 | snp | A/G | 0.165289 | 0.235211 | synonymous-codon | Trim80 | Mm_Celera | 11:115446507 | GCCAGAGACCCTGTC[A/G]CAGCTCCGGATCAGG | 432613 |
rs27031538 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Trim80 | GRCm38.p3 | 11:115446253 | GCCAGGCTACCATTG[A/G]AACCCTAACCTAAGC | 432613 |
rs27031539 | snp | C/T | 0.297521 | 0.245442 | missense | Trim80 | GRCm38.p3 | 11:115441218 | TGCCTGGAGGTGTTC[C/T]GCAACCCAGTCACTA | 432613 |
rs29390148 | snp | C/T | 0.375 | 0.216506 | intron-variant | Trim80 | GRCm38.p3 | 11:115442098 | GAGCTGCATAGCGAG[C/T]TTTTAAGATTTATTT | 432613 |
rs29394241 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon, nc-transcript-variant | Trim80, Mir3968 | GRCm38.p3 | 11:115448001 | TTCGCTCAAGTTCTC[C/T]GTGTGGCACAACAAC | 432613 |
rs29417633 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB | Trim80 | Mm_Celera | 11:115439250 | TGGTGGCTCACAACC[A/G]TCTGTAACGAGATCT | 432613 |
rs29418930 | snp | C/G | 0.375 | 0.216506 | upstream-variant-2KB | Trim80 | GRCm38.p3 | 11:115439819 | TTTGGTGTGCTGGGC[C/G]GTAGTGCCGCACGCC | 432613 |
rs29421248 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Trim80 | GRCm38.p3 | 11:115446365 | GGCAGGTGCCTGACC[A/C]CCGGCTAAGGGGTTA | 432613 |
rs29432486 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Trim80 | GRCm38.p3 | 11:115438563 | ATGGGGGAGCCGGGC[A/G]TACTTTTAATCCCAT | 432613 |
rs29452468 | snp | C/G | 0.375 | 0.216506 | intron-variant | Trim80 | GRCm38.p3 | 11:115445135 | AGCTACCACTGCCTC[C/G]ACCCAGGCTTATCCC | 432613 |
rs29452499 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Trim80 | GRCm38.p3 | 11:115439868 | GAGGCAGAGGCAGGC[A/G]GATTTCTGAGTTCGA | 432613 |
rs29453356 | snp | A/G | 0.5 | 0 | intron-variant | Trim80 | Mm_Celera | 11:115444875 | TTAAAAAGAAAAGAA[A/G]GAAAAGAAAAGACAA | 432613 |
rs29455331 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Trim80 | GRCm38.p3 | 11:115439543 | TCAGAAGGACAGGAA[A/G]TAAGCCACAAGCCAC | 432613 |
rs29457626 | snp | C/G | 0.375 | 0.216506 | intron-variant | Trim80 | Mm_Celera | 11:115442410 | GTCAGAAGTCTCTAT[C/G]AATAGTGAATGATGT | 432613 |
rs29473110 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Trim80 | GRCm38.p3 | 11:115441256 | CGGCCATAACTTCTG[C/T]ATGACTTGCCTTCAG | 432613 |
rs29484996 | snp | A/T | 0.375 | 0.216506 | intron-variant | Trim80 | Mm_Celera | 11:115442411 | TCAGAAGTCTCTATG[A/T]ATAGTGAATGATGTG | 432613 |
rs48171062 | snp | A/G | | | synonymous-codon | Trim80 | GRCm38.p3 | 11:115445433 | GGCGGCCGCCCTAGG[A/G]AAGCTGGGCAACTCT | 432613 |
rs212030774 | snp | G/T | | | intron-variant | Trim80 | Mm_Celera | 11:115442987 | GCGCTTGTGTGGCAG[G/T]CCTCAGAGGAAGGCA | 432613 |
rs212128586 | snp | A/G | | | upstream-variant-2KB | Trim80 | Mm_Celera | 11:115440035 | AGGACCTAGGTTCCA[A/G]TCCAAACACTCACAC | 432613 |
rs212213658 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | Trim80, Mir3968 | GRCm38.p3 | 11:115448417 | GAATGAAAGTCGGTG[A/G]CCCACCTGCTTCCAA | 432613 |
rs212300275 | snp | C/T | | | intron-variant | Trim80 | Mm_Celera | 11:115440612 | CGGTCCACAGGTAGG[C/T]ACAAGAGGATGCGGG | 432613 |
rs212508141 | in-del | -/CA | | | intron-variant | Trim80 | Mm_Celera | 11:115442278 | CTGTCTATTGGTGCC[-/CA]CACACGCCCCTACAA | 432613 |
rs213265612 | in-del | -/T | | | intron-variant | Trim80 | Mm_Celera | 11:115443399 | ATCTAGGCAAAGACA[-/T]TAAAAAAAAAATTAC | 432613 |
rs213513383 | in-del | -/A | | | downstream-variant-500B, upstream-variant-2KB | Trim80, Mir3968 | Mm_Celera | 11:115448740 | TTGGCAGAGTTCTCT[-/A]AGCTTATCTGAGGAC | 432613 |
rs213673037 | snp | G/T | | | intron-variant | Trim80 | Mm_Celera | 11:115445005 | ACTCACTTCTGCCCC[G/T]CCCCTTCCAGGTGGA | 432613 |
rs213924786 | snp | C/T | | | missense, upstream-variant-2KB | Trim80, Mir3968 | Mm_Celera | 11:115448138 | TCTACCGCTTCCTCA[C/T]CTCCTTCCTCGAACC | 432613 |
rs214167857 | snp | C/T | | | upstream-variant-2KB | Trim80 | Mm_Celera | 11:115439394 | TCCACAAAGAGCTTG[C/T]AGCAGACACTGTAGT | 432613 |
rs214232956 | snp | C/T | | | upstream-variant-2KB | Trim80 | Mm_Celera | 11:115440063 | CACAGGGACTCATAG[C/T]CATCTGTAACTCCAG | 432613 |
rs214347910 | snp | G/T | | | upstream-variant-2KB | Trim80 | Mm_Celera | 11:115438656 | TCAAGGCCAGTCTAG[G/T]CAGCTTAAGTAACCC | 432613 |
rs214459779 | snp | A/T | | | intron-variant | Trim80 | Mm_Celera | 11:115447312 | GGAAGGAGGAAGGGG[A/T]CCCCTATTCCCCAGC | 432613 |
rs214560304 | snp | G/T | | | intron-variant | Trim80 | Mm_Celera | 11:115443101 | TTCCAGGCTATCTAG[G/T]CTTAAACATAATGTG | 432613 |
rs214828889 | snp | A/G | | | intron-variant | Trim80 | Mm_Celera | 11:115443362 | GGTCTCCACCGGCAC[A/G]CACAGGGTACACAGA | 432613 |
rs215233357 | in-del | -/GCGTGGTGAC | | | intron-variant | Trim80 | Mm_Celera | 11:115441979 | TGGAAGGAAAGTGGG[-/GCGTGGTGAC]GCGCGCGTCTTTAAT | 432613 |
rs215261416 | snp | A/G | | | intron-variant | Trim80 | Mm_Celera | 11:115442191 | TGGAAATTGAACTCA[A/G]GACCTTCAGAAGAGC | 432613 |
rs215432833 | snp | A/C | | | intron-variant | Trim80 | Mm_Celera | 11:115445161 | ATCCCGGCATCTTCC[A/C]CGGGGCCCCTGGGAC | 432613 |
rs215567165 | snp | A/G | | | intron-variant | Trim80 | Mm_Celera | 11:115445878 | GGGTGGGAAGCCAAG[A/G]CACAGTGGCTGACCA | 432613 |
rs215809077 | in-del | -/C | | | intron-variant | Trim80 | Mm_Celera | 11:115443538 | AACTTGCTCCTCCTT[-/C]CCCCCCACATTAAAA | 432613 |
rs215920792 | snp | C/T | | | intron-variant | Trim80 | Mm_Celera | 11:115442259 | CGAGACCCAACTCCT[C/T]AAAGCTGTCTATTGG | 432613 |
rs215986803 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB | Trim80, Mir3968 | Mm_Celera | 11:115448267 | TAAAGTTAGACTCTA[C/T]GTACTGCTGTGCAGG | 432613 |
rs216053763 | snp | C/T | | | upstream-variant-2KB | Trim80 | Mm_Celera | 11:115439928 | GGACAGCCAGGGCTA[C/T]ACAGAGAAACCCTGT | 432613 |
rs216343893 | snp | A/G | | | intron-variant | Trim80 | Mm_Celera | 11:115443515 | GTTCAAGGTCATCTC[A/G]GCTACATAAACTTGC | 432613 |
rs216445963 | in-del | -/G | | | intron-variant | Trim80 | Mm_Celera | 11:115442706 | GTTTTGTTTTGTTTT[-/G]TTTTTTTCGAGACAG | 432613 |
rs217415871 | snp | A/G | | | upstream-variant-2KB | Trim80 | Mm_Celera | 11:115439547 | AAGGACAGGAAGTAA[A/G]CCACAAGCCACTAAA | 432613 |
rs217619271 | in-del | -/TCTTACTC | | | downstream-variant-500B, upstream-variant-2KB | Trim80, Mir3968 | Mm_Celera | 11:115448640 | CCCATCCCTGTCACT[-/TCTTACTC]TCTTCAGACTGGGCA | 432613 |
rs217850476 | snp | C/T | | | upstream-variant-2KB | Trim80 | Mm_Celera | 11:115440244 | GTATGATGCTTGGGT[C/T]ATTAGTTAGCCCAGA | 432613 |
rs217958515 | snp | G/T | | | missense | Trim80 | Mm_Celera | 11:115441451 | GGCTGGCCCCACAGA[G/T]GTGCCCTGTGACTTT | 432613 |
rs218731470 | in-del | -/T | | | intron-variant | Trim80 | Mm_Celera | 11:115442702 | TTTTGTTTTGTTTTG[-/T]TTTTTTTTTTTCGAG | 432613 |
rs219058067 | snp | A/C/T | | | downstream-variant-500B, upstream-variant-2KB | Trim80, Mir3968 | Mm_Celera | 11:115448334 | ATAGAGGCACAAGGG[A/C/T]GCCAGGGTCATTGTT | 432613 |
rs219583112 | snp | C/G | | | intron-variant | Trim80 | Mm_Celera | 11:115447228 | CAGGAACCCTTCACT[C/G]TCCCCAAGTCTCATT | 432613 |
rs219921064 | in-del | -/T | | | intron-variant | Trim80 | Mm_Celera | 11:115445770 | TAATTCAGTCTCCCC[-/T]CCCAAACCACAGGCA | 432613 |
rs220699387 | snp | A/G | | | intron-variant | Trim80 | Mm_Celera | 11:115447392 | TATTTTAAGAAGTAG[A/G]TAGAGCCAGGTGTGG | 432613 |
rs220730675 | snp | C/T | | | intron-variant | Trim80 | Mm_Celera | 11:115446636 | CTCTAGTGGTTGTGG[C/T]GCCCCACCTGCCTGT | 432613 |
rs221004113 | snp | A/G | | | synonymous-codon | Trim80 | Mm_Celera | 11:115445430 | GGAGGCGGCCGCCCT[A/G]GGAAAGCTGGGCAAC | 432613 |
rs221142571 | snp | C/T | | | intron-variant | Trim80 | Mm_Celera | 11:115443683 | GGCGGTGGTGGTGCA[C/T]GCCTTTGATCCCAGC | 432613 |
rs221171776 | snp | C/G | | | intron-variant | Trim80 | Mm_Celera | 11:115443285 | TGGCTCGGTCATTAA[C/G]AAACCTGGGTTCAGT | 432613 |
rs221399155 | snp | A/C | | | intron-variant | Trim80 | Mm_Celera | 11:115443191 | GGGTTCAAGCCTAGC[A/C]TGGTCTACATAGCTA | 432613 |
rs221476608 | snp | A/T | | | downstream-variant-500B, upstream-variant-2KB | Trim80, Mir3968 | Mm_Celera | 11:115448515 | TGGAAGGGTTCTAAA[A/T]CAGACTGAAGGTCTC | 432613 |
rs221548332 | snp | C/T | | | upstream-variant-2KB | Trim80 | Mm_Celera | 11:115440237 | GAATGATGTATGATG[C/T]TTGGGTCATTAGTTA | 432613 |
rs221585588 | snp | A/G | | | upstream-variant-2KB | Trim80 | Mm_Celera | 11:115439790 | GGAAATACTGGAGAG[A/G]TGGATTAAGAGCATT | 432613 |
rs221767782 | snp | C/T | | | intron-variant | Trim80 | Mm_Celera | 11:115442726 | TTTCGAGACAGGGTT[C/T]CTCTGTGTAGCCCTG | 432613 |
rs221793418 | snp | A/T | | | upstream-variant-2KB | Trim80 | Mm_Celera | 11:115439009 | CGCTATTGCTGATGC[A/T]ACACACCCTGGACAC | 432613 |
rs221847643 | snp | A/G | | | intron-variant, downstream-variant-500B | Trim80, Mir3968 | Mm_Celera | 11:115447578 | GTGAGATCTTTGCAA[A/G]CATCGTTGCAAAAAC | 432613 |
rs222076514 | in-del | -/AAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAG/AAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAG | | | intron-variant | Trim80 | Mm_Celera | 11:115444548 | AACAGTGTCTCAAAA[lengthTooLong]AAAGAAAGAAAGAAA | 432613 |
rs222243587 | snp | A/G | | | intron-variant | Trim80 | Mm_Celera | 11:115443157 | CAACATTTGGGACGC[A/G]AAGCAGGGAGATGGC | 432613 |
rs222288975 | snp | C/T | | | intron-variant | Trim80 | Mm_Celera | 11:115442585 | CAAACCAGAGGACCC[C/T]GGCTTTGACTCCCAC | 432613 |
rs222317189 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB | Trim80, Mir3968 | Mm_Celera | 11:115448399 | CATGGTCCCATGCGT[C/T]AAGAATGAAAGTCGG | 432613 |
rs222380960 | in-del | -/TA | | | intron-variant | Trim80 | Mm_Celera | 11:115444127 | AGGCAAAACATACAC[-/TA]TATATATATATATGT | 432613 |
rs222430702 | snp | C/T | | | upstream-variant-2KB | Trim80 | Mm_Celera | 11:115439690 | CCTGGGGATGTAACT[C/T]AGCGGTACAGCGTTT | 432613 |
rs222670361 | snp | C/T | | | upstream-variant-2KB | Trim80 | Mm_Celera | 11:115438947 | TATGTGGTGTGGCTC[C/T]GTGCAGCAGGCAAAC | 432613 |
rs222726440 | snp | A/G | | | intron-variant | Trim80 | Mm_Celera | 11:115442499 | ACCTGTGCAGGACGC[A/G]CCTGCGCCTTTCTCC | 432613 |
rs223058645 | in-del | -/A | | | upstream-variant-2KB | Trim80 | Mm_Celera | 11:115439974 | AACAAAAACAAAAAC[-/A]AAAACAAAACAAACA | 432613 |
rs223518814 | snp | A/T | | | intron-variant | Trim80 | Mm_Celera | 11:115443727 | AGGCAAGCGGATTTC[A/T]GAGTTTGAGGCCAGC | 432613 |
rs223624709 | snp | C/T | | | intron-variant | Trim80 | Mm_Celera | 11:115445179 | GGGCCCCTGGGACCT[C/T]CCAGAAGCCACGGGA | 432613 |
rs223802029 | snp | C/G | | | missense | Trim80 | Mm_Celera | 11:115441666 | GCACGGAGGGCAGCT[C/G]CGTGTGCGGAGCCTG | 432613 |
rs223949294 | in-del | -/ATATATATATATATGTATATATATATATATATATATATAC | | | intron-variant | Trim80 | Mm_Celera | 11:115444128 | GGCAAAACATACACT[lengthTooLong]ATATATATATATGTA | 432613 |
rs225026328 | snp | A/T | | | upstream-variant-2KB | Trim80 | Mm_Celera | 11:115438810 | ACTTTGTATTTTTGT[A/T]ATTAAACCATTATGT | 432613 |
rs226019424 | snp | A/G | | | intron-variant | Trim80 | Mm_Celera | 11:115444565 | AAGAAAGAAAGAAAG[A/G]AAGAAAGGAAGAAAG | 432613 |
rs226272093 | snp | A/G | | | synonymous-codon, upstream-variant-2KB | Trim80, Mir3968 | Mm_Celera | 11:115448151 | CACCTCCTTCCTCGA[A/G]CCCCTGTACCCCGCG | 432613 |
rs226392784 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | Trim80, Mir3968 | Mm_Celera | 11:115448689 | CTTCTCTCTCCAGGT[A/G]GCCATTCTGTGAAGT | 432613 |
rs226553170 | snp | C/T | | | intron-variant, downstream-variant-500B | Trim80, Mir3968 | Mm_Celera | 11:115447468 | CAAGGTCAGCCTAGG[C/T]TAACCTGGGCTCAAC | 432613 |
rs226644933 | snp | G/T | | | intron-variant | Trim80 | Mm_Celera | 11:115443370 | CCGGCACGCACAGGG[G/T]ACACAGACATTACAT | 432613 |
rs226715046 | snp | A/G | | | missense | Trim80 | Mm_Celera | 11:115445515 | CTCCACAGCCTGCTC[A/G]CCAACAGGAGTGATG | 432613 |
rs226751477 | snp | C/G | | | intron-variant | Trim80 | Mm_Celera | 11:115444764 | TTCAATTCCAAGCAA[C/G]GACATGGTGGCTCAC | 432613 |
rs227031864 | snp | A/G | | | intron-variant | Trim80 | Mm_Celera | 11:115446715 | GTCTGGAAGGAGGCT[A/G]GGCTGTAAGAGTGGC | 432613 |
rs227698817 | snp | A/T | | | intron-variant | Trim80 | GRCm38.p3 | 11:115443596 | TAGGAGGTTGCTCAG[A/T]AAGTAAAGTGCTTGA | 432613 |
rs228004455 | snp | C/T | | | synonymous-codon, upstream-variant-2KB | Trim80, Mir3968 | Mm_Celera | 11:115448079 | GCTGGACTTCAGGAC[C/T]GGCTGCCTGTCCTTC | 432613 |
rs228319525 | snp | C/T | | | intron-variant | Trim80 | Mm_Celera | 11:115447042 | TACTTCAGAGACGGC[C/T]CTTCCATGGCTCTCA | 432613 |
rs228541421 | snp | A/G | | | intron-variant | Trim80 | Mm_Celera | 11:115442958 | CCTTCATTAAGCATC[A/G]CTCCCGGATCCAAGC | 432613 |
rs228733547 | snp | A/G | | | intron-variant | Trim80 | Mm_Celera | 11:115444137 | ATACACTATATATAT[A/G]TATGTATATTCATAC | 432613 |
rs228740283 | snp | C/T | | | intron-variant | Trim80 | Mm_Celera | 11:115441807 | TCACATTTCGGGGGG[C/T]GGGGATGAACACAGC | 432613 |
rs228745470 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB | Trim80, Mir3968 | Mm_Celera | 11:115448605 | CTTCCCCGACCCCAT[C/T]GGCAACCCTTGCTTC | 432613 |
rs228776613 | snp | A/G | | | upstream-variant-2KB | Trim80 | Mm_Celera | 11:115440492 | GGACTGGCCGCACCT[A/G]AATTATGACATCAGC | 432613 |
rs228865826 | snp | C/T | | | intron-variant | Trim80 | Mm_Celera | 11:115440624 | AGGCACAAGAGGATG[C/T]GGGACGCCCTCAGAG | 432613 |