SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6390079 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705890 | GCATAAGAGAGCCCA[C/T]AGAAAGGNTTCAACC | 16897 |
rs6390096 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705898 | GAGCCCANAGAAAGG[G/T]TTCAACCTGTTCTGC | 16897 |
rs6404373 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60706160 | CTCCCATTTCTGGGA[A/C]GTTCTCCTGACTCTC | 16897 |
rs6405013 | snp | C/T | 0.5 | 0 | synonymous-codon, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60706307 | GGGTTTACTGGTCAT[C/T]TGGAGCCAGGCCACA | 16897 |
rs6405993 | snp | A/G | 0.5 | 0 | synonymous-codon, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60706443 | TCATCCATAGCAGCT[A/G]GAGAGCCTGTGTTGG | 16897 |
rs13461715 | snp | C/T | | | synonymous-codon | Llgl1 | GRCm38.p3 | 11:60712661 | CCAGGCTAATGGGAC[C/T]AGAGACATCATTCTG | 16897 |
rs26972021 | snp | A/G | 0.197531 | 0.244432 | downstream-variant-500B, synonymous-codon | Llgl1, Flii | GRCm38.p3 | 11:60714367 | GCAGCGGGTGAAGGC[A/G]CGCTGCTCATTACCT | 16897 |
rs26972022 | snp | C/G | 0.142012 | 0.225474 | utr-variant-3-prime | Llgl1 | GRCm38.p3 | 11:60713594 | TAGTAGCTAGTGCCT[C/G]TGCAGCCTACATTGG | 16897 |
rs26972023 | snp | A/G | 0.165289 | 0.235211 | utr-variant-3-prime | Llgl1 | GRCm38.p3 | 11:60713304 | ATGGTGTCATTCCTC[A/G]AAGCCTAGCTGCCTT | 16897 |
rs26972024 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Llgl1 | GRCm38.p3 | 11:60712506 | CAGGTTTGTGAGGAA[C/T]GGGTCCCTTAGCCGC | 16897 |
rs26972025 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Llgl1 | GRCm38.p3 | 11:60711827 | CTGGCCAAGGGTGGA[A/G]ATGAGGCTCATGGTG | 16897 |
rs26972026 | snp | C/G | 0.396694 | 0.202437 | intron-variant | Llgl1 | GRCm38.p3 | 11:60711644 | AAGGTGAGCTGCCTT[C/G]GGTGATGAGGATCCA | 16897 |
rs26972027 | snp | A/C | 0.396694 | 0.202437 | intron-variant | Llgl1 | GRCm38.p3 | 11:60710745 | GACTCTGTGGGAGCA[A/C]GTCCTCTCTGTGCTT | 16897 |
rs26972028 | snp | C/T | 0.21875 | 0.248039 | synonymous-codon | Llgl1 | GRCm38.p3 | 11:60710304 | GCAGGAGGCCAATGC[C/T]CAGCTGGCCGAGCAG | 16897 |
rs26972029 | snp | A/C | 0.42 | 0.183303 | intron-variant | Llgl1 | GRCm38.p3 | 11:60709947 | GCAGGAGTGCAGTGT[A/C]GCTCCATAGCACAGT | 16897 |
rs26972030 | snp | A/G | 0.375 | 0.216506 | intron-variant | Llgl1 | GRCm38.p3 | 11:60709873 | GCGGGAGAACGGGTC[A/G]GCTCTTGGAGCTGCT | 16897 |
rs26972031 | snp | A/C | 0.18 | 0.24 | intron-variant | Llgl1 | GRCm38.p3 | 11:60709803 | ATTCCGTTTCCTTTC[A/C]GAGGTTGTGCAGAAG | 16897 |
rs26972032 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Llgl1 | GRCm38.p3 | 11:60709790 | AAGGTGGTCTGGGAT[C/T]CCGTTTCCTTTCAGA | 16897 |
rs26972033 | snp | C/G | 0.42 | 0.183303 | synonymous-codon | Llgl1 | GRCm38.p3 | 11:60709557 | GCTGAACCCACACAC[C/G]GGGCTGCTGCCGTGG | 16897 |
rs26972034 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Llgl1 | GRCm38.p3 | 11:60709536 | CACGTGGAAGGGTCA[C/T]GAGCGGCTGAACCCA | 16897 |
rs26972035 | snp | A/G | 0.244898 | 0.249948 | synonymous-codon | Llgl1 | GRCm38.p3 | 11:60709458 | GCTGGAGCTCAGTGA[A/G]GTCCCAGCAGAGCAT | 16897 |
rs26972036 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Llgl1 | GRCm38.p3 | 11:60709353 | CTCAGTGAAGGCTTT[A/G]GTACATTGTAGGTAT | 16897 |
rs26972037 | snp | A/C | 0.375 | 0.216506 | intron-variant | Llgl1 | GRCm38.p3 | 11:60709210 | GCCTAGCGGGTCTGT[A/C]ACAGAGTACCTGTGC | 16897 |
rs26972038 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Llgl1 | GRCm38.p3 | 11:60709159 | TGAGGCTGGGAGCAG[A/G]AATATAGCTGTGCAG | 16897 |
rs26972039 | snp | A/G | 0.375 | 0.216506 | intron-variant | Llgl1 | GRCm38.p3 | 11:60709052 | GGAACACCAGGGAAG[A/G]TTGGCAGGGGTGAGG | 16897 |
rs26972040 | snp | A/G | 0.375 | 0.216506 | synonymous-codon | Llgl1 | GRCm38.p3 | 11:60708875 | AGCCCAGATGGTGGT[A/G]GCTGGCACTGCAGGC | 16897 |
rs26972041 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Llgl1 | GRCm38.p3 | 11:60708574 | TGTGCGGTTCTGGGA[C/T]GCCTCTGGTGTGGCG | 16897 |
rs30717390 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60698459 | ATGTTGGATTTCAAC[C/T]TTGCAAATGCTCAGG | 16897 |
rs30871118 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60698778 | GGACCTAGCTACCTC[C/T]AAACTGCCCACGACC | 16897 |
rs30929029 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60699280 | GGCAGGCAGATCTCT[C/T]TGAGTTCCAGGCCAG | 16897 |
rs31015065 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60698836 | TTTGTCAAGAGAGGA[A/G]GCGTTGACCCTTAAC | 16897 |
rs45681298 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60710205 | GCCGTGGGCCCTGTA[A/G]GGTGAAGGGATCCTG | 16897 |
rs45715980 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Llgl1, Flii | GRCm38.p3 | 11:60713674 | CCAGCAAGCCCATCT[C/T]GGGCCATCACTGAAA | 16897 |
rs45834987 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60710204 | TGCCGTGGGCCCTGT[A/G]GGGTGAAGGGATCCT | 16897 |
rs45867128 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60706661 | AAATCTACAGAAGGA[A/G]CCTCCGGGGGGCATC | 16897 |
rs45872802 | snp | A/G | | | synonymous-codon, utr-variant-5-prime | Llgl1 | GRCm38.p3 | 11:60706542 | TGGCAGCCCCCCAAC[A/G]CTGCAGCCCACTGTA | 16897 |
rs45900155 | snp | A/G | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705401 | GGTGTGTACCCCCAT[A/G]TTTGACCTTCCTGCT | 16897 |
rs46104130 | snp | C/T | | | synonymous-codon, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60706205 | CAGTGTGCCAGATGA[C/T]TACCGGTGTGGAAAG | 16897 |
rs46142401 | snp | C/T | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705060 | GCTCTGCTGAAGCAG[C/T]GCAGACACAGTTGGG | 16897 |
rs46152808 | snp | G/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60710789 | CTTTGGTTTTTACGT[G/T]GTATCATACTAAGTA | 16897 |
rs46425545 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60708352 | CTGGTTGTCAAAGTG[A/G]TCATTCCTTTACCTT | 16897 |
rs46718780 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60708276 | TAGGCTTCTTGCCTG[A/G]CCTGGGGTTTGTGGC | 16897 |
rs46750864 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60712827 | GCCAGGGCTGGAGGG[C/T]GCCTGTGTGTGCACA | 16897 |
rs46791653 | snp | C/T | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60706152 | GGAGGACCCTCCCAT[C/T]TCTGGGAAGTTCTCC | 16897 |
rs46905213 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60701016 | AAGAAGAGAGTGGGT[C/T]TTAGCCAGTGAATGG | 16897 |
rs47463409 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700327 | CTCTGCCCTACCTTG[A/G]GGTCCCTAGTTCAAG | 16897 |
rs47517908 | snp | C/T | | | synonymous-codon | Llgl1 | GRCm38.p3 | 11:60702834 | CTTGGCCTTCGATCC[C/T]GAGCTCCGCATCATG | 16897 |
rs47978447 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60706638 | GGCCTTGAGGGTACT[A/G]CATAGCCAAATCTAC | 16897 |
rs48319120 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60711855 | GTGAAGCCTGGGCTG[C/T]TCTGTAGGCCATCTG | 16897 |
rs48526412 | snp | A/G | | | downstream-variant-500B, intron-variant | Llgl1, Flii | GRCm38.p3 | 11:60714486 | GGGTAGTCCTCTAAG[A/G]CCTGCTGGACTGACC | 16897 |
rs48762726 | snp | C/T | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705118 | GAACCCTTCTTGAAG[C/T]GGTATCCTTTGAAGA | 16897 |
rs48768806 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60707737 | GGTGCTGAAGTGCTC[A/G]GTGACTCAGTCTCAG | 16897 |
rs48989582 | snp | A/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60701009 | ATGAAACAAGAAGAG[A/T]GTGGGTTTTAGCCAG | 16897 |
rs49011847 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703863 | GATCCTCCTTCTCTT[C/T]CCTTTTTCCTCTCAA | 16897 |
rs49196931 | snp | G/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703038 | GAGGGTCTTTTGGTT[G/T]GGAGATGGGTGATTG | 16897 |
rs49280021 | snp | C/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700414 | CCGCCATGAAATGAG[C/G]CCAGTTTCCCCCTTG | 16897 |
rs49305426 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700849 | CACTTTCAGGGGGAG[A/G]CCCTGCCATGGCTCA | 16897 |
rs49538633 | snp | C/T | | | utr-variant-3-prime | Llgl1 | GRCm38.p3 | 11:60713636 | TAACCATACCCTCTT[C/T]TACTTGGTACCCTCC | 16897 |
rs49546218 | snp | G/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60706867 | AGAGGATTAGGCTCC[G/T]GGTATATAGGGGTGC | 16897 |
rs49558309 | snp | C/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60701178 | GGTCATCTTGGGGAA[C/G]GAGTTTGATTGCCAC | 16897 |
rs49651086 | snp | A/C | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60704371 | TGGTCCGTGCAGGTG[A/C]ATCCGCGGCCTCGTG | 16897 |
rs49694472 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | Llgl1, Flii | GRCm38.p3 | 11:60714256 | GGCTGTGGCTAGCTG[A/G]AGCAGGTACGAGGAG | 16897 |
rs49944457 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60711929 | GATTGAGGCCTGCAG[A/G]GCCAGGTGGGTGTCT | 16897 |
rs49957478 | snp | A/C | | | downstream-variant-500B, intron-variant | Llgl1, Flii | GRCm38.p3 | 11:60714491 | GTCCTCTAAGGCCTG[A/C]TGGACTGACCACTGT | 16897 |
rs50062927 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703322 | CCCCCATCTGGACAC[C/T]GATGCCATACAATGG | 16897 |
rs50324014 | snp | A/G | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705875 | TGTGAATGCAGAGAG[A/G]CATAAGAGAGCCCAT | 16897 |
rs50430856 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60710232 | CCTGCTGGACACGGG[A/G]CAGAGGGCTCTTGGA | 16897 |
rs50465683 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Llgl1, Flii | GRCm38.p3 | 11:60713704 | AGGGGCTGCCTACCC[C/T]GCAGGCAGGCATGAC | 16897 |
rs50647563 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60708213 | CCTCTCCCTACTTTC[C/T]CCTCGTTTGACACCC | 16897 |
rs50675716 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700151 | ACCTATCTGCCTTTC[A/G]CTCTTGGCCTCTTTT | 16897 |
rs50779505 | snp | C/T | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705443 | TTGGGATCGGCTGGG[C/T]CATGGTTGATAGTCG | 16897 |
rs50926125 | snp | A/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700671 | TTCCATTACACACGT[A/T]AAAAAACAAACAAAC | 16897 |
rs51201788 | snp | A/G | | | upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60699548 | AGCTCAGTCGTGAGT[A/G]GAAAACAACCTTTAG | 16897 |
rs51256638 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Llgl1, Flii | GRCm38.p3 | 11:60713697 | CACTGAAAGGGGCTG[C/T]CTACCCCGCAGGCAG | 16897 |
rs51331605 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60706909 | GGTTATCCAGCATGT[A/G]CCCTGCACTCCCGGA | 16897 |
rs51363723 | snp | A/G | | | utr-variant-3-prime, intron-variant | Llgl1 | GRCm38.p3 | 11:60713115 | CCAGCCCTTCTGATT[A/G]CTGCCCTCCCCAGCT | 16897 |
rs51487498 | snp | C/T | | | synonymous-codon | Llgl1 | GRCm38.p3 | 11:60707287 | GTGCCCGCCCCTTAC[C/T]TGGCCCCACTGCATT | 16897 |
rs51593140 | snp | A/G | | | synonymous-codon | Llgl1 | GRCm38.p3 | 11:60709464 | GCTCAGTGAGGTCCC[A/G]GCAGAGCATGCCGTC | 16897 |
rs51728044 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Llgl1, Flii | GRCm38.p3 | 11:60713693 | CCATCACTGAAAGGG[A/G]CTGCCTACCCCGCAG | 16897 |
rs51978171 | snp | C/T | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705876 | GTGAATGCAGAGAGG[C/T]ATAAGAGAGCCCATA | 16897 |
rs52256631 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B | Llgl1, Flii | GRCm38.p3 | 11:60714109 | TTTTCTGTCTTTTTT[A/T]AAAAACTAGTTGTTT | 16897 |
rs107611484 | snp | A/C | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60702292 | CCTGCCACCCCACCT[A/C]TCCCTCCCCGATGGC | 16897 |
rs107721081 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60702397 | TCCTCTATCTTGGGA[C/T]CCTCCTGTCTTAGCG | 16897 |
rs108018224 | snp | A/T | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705583 | GCTGCAATGGGATAG[A/T]CTTTGCCCACAGGTT | 16897 |
rs211731640 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60701622 | AGTGTGGTCGGGGGG[A/G]GGGGGGTGCGGGGGG | 16897 |
rs211749842 | snp | A/G | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60697776 | AGCAGCCAAATGGTT[A/G]CTTGCAATTGATCTC | 16897 |
rs212034883 | snp | A/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60707798 | TTAGGAAGCCTCCCT[A/T]GATTCTGGCTCAAAG | 16897 |
rs212064431 | snp | A/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60708435 | CTATTCTTCCTGCAT[A/T]GTGGGTGCTTACTGC | 16897 |
rs212095008 | snp | A/G | | | synonymous-codon | Llgl1 | GRCm38.p3 | 11:60710020 | TTTGGCCATGGAGGG[A/G]CCACTGTCACGGGTG | 16897 |
rs212307837 | snp | A/C | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700687 | AAAAAACAAACAAAC[A/C]AACAAAAAAAAAAAA | 16897 |
rs212494476 | in-del | -/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60707697 | AGGAGGCCTTATTTG[-/T]TTTCTGAGCATCCCA | 16897 |
rs212522149 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60710724 | CTGGTGCTGCCATCA[C/T]TCAGGGACTCTGTGG | 16897 |
rs213516959 | snp | A/C | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700530 | CCTCAGCTCCCACCT[A/C]GTCTGCACTGACCAG | 16897 |
rs213533890 | snp | A/G | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705138 | TCCTTTGAAGATAGG[A/G]TTAGAGGTGTGGCCA | 16897 |
rs213546906 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60709910 | ACAAGCCCTAGCTCC[A/G]GTTGCTCTGGCCCCC | 16897 |
rs213741027 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60702921 | CTCACTTCATGCTGG[A/G]GTCTTAGCATGGCAG | 16897 |
rs214034143 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60701693 | GCTGCCTAGCCAAAG[A/G]GCCAAGTGCTTTGGG | 16897 |
rs214105237 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60707749 | CTCAGTGACTCAGTC[C/T]CAGTCCTAGTGAATC | 16897 |
rs214123837 | snp | C/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60711044 | CCCAGCCTTGCAGGA[C/G]GCACTGCGTTTGCTG | 16897 |
rs214382008 | in-del | -/GGCCTGCA | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60708902 | AGGCCAGGTGCGGTT[-/GGCCTGCA]GTCTCCAGATGTGGT | 16897 |
rs214528651 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60709393 | ATTTGCTGGGTAGGT[A/G]AGTTCTGGGGCCACT | 16897 |
rs214585705 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60712340 | TTGGCGGTGGCAGTG[C/T]CCCTTAAATATTCCT | 16897 |
rs215430760 | snp | A/G | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705180 | GGCCAGTGGGCAGAG[A/G]CTGTGTTTCCCACCG | 16897 |
rs215628738 | in-del | -/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700268 | GGAAAAGTGGGGGGT[-/G]GGGGGGGCTGGGAAA | 16897 |
rs215636535 | in-del | -/GT | | | utr-variant-3-prime, downstream-variant-500B | Llgl1, Flii | GRCm38.p3 | 11:60714020 | TGAAGTCAGTCAGAG[-/GT]GTGTGTGTGCGTGTG | 16897 |
rs216001047 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60710758 | CACGTCCTCTCTGTG[C/T]TTCATGTTGGCGGTT | 16897 |
rs216028549 | in-del | -/TTTTC | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60699219 | CTCAAGGAATTGAGA[-/TTTTC]TTTTTTTTTTTTGAG | 16897 |
rs216240468 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60710163 | CATGTCCGTGCCCTG[A/G]CCCAGAGTGCTCCGG | 16897 |
rs216534965 | in-del | -/TTTG | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60698317 | TGGTGTTTGGGGTTT[-/TTTG]TTTGTTTGTTTGTTT | 16897 |
rs216704447 | snp | C/G | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60699040 | TTCCCTGTAGGGATG[C/G]GGGAAACAAGGGGAG | 16897 |
rs216749787 | snp | A/C/G/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60701631 | GGGGGGGGGGGGGTG[A/C/G/T]GGGGGGGGGAACAGA | 16897 |
rs216986532 | snp | A/C | | | upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60697865 | CCTTAAAAGTCATTC[A/C]TTTTCTTTTTCTTTT | 16897 |
rs217026781 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60708707 | CGCAAGGTGCCTCTC[C/T]TCCCTCCCCCTGCCC | 16897 |
rs217264845 | in-del | -/TC | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60708211 | TTCCTCTCCCTACTT[-/TC]TCCTCGTTTGACACC | 16897 |
rs217415784 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60702516 | GGTGGGCCAGTGGGA[A/G]GAGGCACAGTCACAC | 16897 |
rs217664597 | in-del | -/A | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60698848 | GCCTCCTCTCTTGAC[-/A]AAAGATGGGAGGACA | 16897 |
rs217687788 | snp | A/G | | | missense, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60706338 | CAGTCTGTGGACAAC[A/G]TTTTCCTAGGTAACC | 16897 |
rs217753722 | snp | C/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60707669 | TATGGGTGGCAGACA[C/G]GGCCCAGCACCTAGG | 16897 |
rs218014919 | snp | C/T | | | synonymous-codon | Llgl1 | GRCm38.p3 | 11:60699914 | GCAGCGCGAGAAGCT[C/T]AAGCAGGAGCTCTTC | 16897 |
rs218027988 | snp | G/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60707758 | TCAGTCTCAGTCCTA[G/T]TGAATCCGATCTGAG | 16897 |
rs218047988 | snp | A/G | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60698161 | GAACTCACTCTGGAG[A/G]CCAGGCTGACCTCGA | 16897 |
rs218366384 | snp | C/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703933 | CTGGAAAGTGCCACA[C/G]TTGGTCTCTAGAGCC | 16897 |
rs218398007 | snp | G/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703402 | GTGGGGCAACAGGCT[G/T]CTGAATGTCTCCTTA | 16897 |
rs218912572 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703872 | TCTCTTCCCTTTTTC[C/T]TCTCAATTCCTGTAG | 16897 |
rs218953621 | snp | C/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60701615 | CCTGCACAGTGTGGT[C/G]GGGGGGGGGGGGGTG | 16897 |
rs219331855 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60709748 | TGGCACGAGGTGGCC[A/G]GGTGGGTGGGCAGCC | 16897 |
rs219422968 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Llgl1, Flii | GRCm38.p3 | 11:60713677 | GCAAGCCCATCTTGG[A/G]CCATCACTGAAAGGG | 16897 |
rs219595219 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703109 | TGCCTTTCAGCCTAC[C/T]AATTCTTAGGTAATC | 16897 |
rs219632913 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703778 | GCCCATGGTCTACAC[C/T]GCCAGGTGCTTAGAG | 16897 |
rs219645650 | snp | C/T | | | missense | Llgl1 | GRCm38.p3 | 11:60712484 | GGCCCCAAAATGCCA[C/T]CCAGCCCAGGTTTGT | 16897 |
rs219784429 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700890 | GTTGCGATCTCAGCA[A/G]TGATCAGGGGGTGCC | 16897 |
rs219837310 | snp | G/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60710239 | GACACGGGGCAGAGG[G/T]CTCTTGGAAGAGCAC | 16897 |
rs220083777 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60708749 | CCTTTGAGCTGGTCA[C/T]AGCTCTGCACTGCAT | 16897 |
rs220112858 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60708177 | TCCCAGTGCTTCACC[C/T]TACTTTTGTCTCCTC | 16897 |
rs220145582 | snp | A/T | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60698046 | AGCAGTCAGTGCTCT[A/T]AACCACTGAGCCATC | 16897 |
rs220159983 | snp | A/G | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705523 | TGTGCATAGCAGGCC[A/G]GGCTCCCCAGGTGGA | 16897 |
rs220237005 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60709427 | CCTCTCTCCTGCTGT[A/G]TGTCCAGGTGCTGGT | 16897 |
rs220451367 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60712588 | AGATGCAGCACCTGT[A/G]ATAGTCTCCATCACA | 16897 |
rs220485420 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60711242 | CTGGTCCCTGCAGCC[A/G]GTTAGGAAATGATGG | 16897 |
rs220552857 | in-del | -/TC | | | downstream-variant-500B, intron-variant | Llgl1, Flii | GRCm38.p3 | 11:60714580 | GGCTGGCTTCAGTAA[-/TC]TCTCTTACCTGGCAA | 16897 |
rs220869098 | snp | C/G/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60708905 | CCAGGTGCGGTTGGC[C/G/T]TGCAGTCTCCAGATG | 16897 |
rs220987571 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60712782 | GTACCTGAGGGAGAG[A/G]GGTTAAGACGTAAGC | 16897 |
rs222163308 | in-del | -/AC | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705942 | AGATGGGCTCACCTT[-/AC]ACTCTCTCTTCCTCT | 16897 |
rs222163599 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60708999 | GGGTGTGGTGAAGTA[A/G]AGGGCAACCAATGTG | 16897 |
rs222293238 | in-del | -/A | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60698534 | TCATGACTTGTGTGG[-/A]GGCTGATCTTGGTCT | 16897 |
rs222385403 | in-del | -/TGGTGC | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60702665 | TATCCCCACCTCTGA[-/TGGTGC]TGGGATTCCTGTTTT | 16897 |
rs222527383 | snp | A/G | | | downstream-variant-500B, synonymous-codon | Llgl1, Flii | GRCm38.p3 | 11:60714352 | GCTCCAGGCGTGGAA[A/G]CAGCGGGTGAAGGCG | 16897 |
rs222932612 | in-del | -/GGAGGT | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60708969 | GGGAGGCTTTCTGCA[-/GGAGGT]GGCCCTGTAGGGTGT | 16897 |
rs223847699 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703266 | TGTTCAACCCAGGGC[A/G]GGAGGGCAGTGCCAG | 16897 |
rs223890427 | snp | G/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60702270 | GCCCAAGACTGCTTG[G/T]GTAGACCCTGCCACC | 16897 |
rs224219030 | snp | A/C | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60701308 | TCAGACCACAAATTA[A/C]AAATTGCCTGTAGGA | 16897 |
rs224285149 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60702301 | CCACCTCTCCCTCCC[C/T]GATGGCTAGCTCCAT | 16897 |
rs224712894 | snp | A/C | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60702908 | TTCTGAGGTGCTGCT[A/C]ACTTCATGCTGGAGT | 16897 |
rs225044800 | snp | A/C | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60704844 | GGTCTCTGCTCCGTC[A/C]CATCAGGGCCGCCTC | 16897 |
rs225080450 | snp | A/C | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703735 | CTGGGTTAGAGGTAT[A/C]CACATCAAAGGTGTC | 16897 |
rs225287966 | snp | G/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700051 | GTCGGGCTGCGCCCC[G/T]CGCCGTGCCGTGCGC | 16897 |
rs225324673 | snp | C/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700764 | TGTGTGATAGCAGTG[C/G]AGTAGGAGTTTTGAA | 16897 |
rs225429877 | snp | C/T | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60697692 | TTTAATGTATGAGTG[C/T]TCCACCTGCATTTTC | 16897 |
rs225465337 | snp | A/C | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705479 | GTTCTCCAGGGTAGG[A/C]TTGGTGAGGTGCTGG | 16897 |
rs225467089 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60708380 | CTTCCAACCTGTTCA[A/G]AAGGCTCTCGGGGCA | 16897 |
rs225495222 | snp | A/G | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60698720 | GCTCGGGAAAGAGCT[A/G]TGAGTCCTGAGCCCC | 16897 |
rs225660115 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60712846 | TGTGTGTGCACATGC[A/G]TGTCCTGTGTGCTCT | 16897 |
rs225887221 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60707988 | GGTGACTCAGGCCTC[A/G]CTAACTGCCCTGCCC | 16897 |
rs226105909 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60704271 | GCTCTGAAGGGAGCT[C/T]GGGGTTCTTGACCAT | 16897 |
rs226367386 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700988 | CTCACCGTGAGGGTG[C/T]GCCCCATGAAACAAG | 16897 |
rs226407468 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60707532 | TGGCCAGGATGAGAG[A/G]GAGACCTTCAGCCTA | 16897 |
rs226532547 | snp | A/G | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60698038 | TCTGGAAGAGCAGTC[A/G]GTGCTCTTAACCACT | 16897 |
rs226791311 | snp | G/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60710499 | TCTGTACTGGGGGGA[G/T]GCGGTGTGAGAAGCA | 16897 |
rs226827021 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60709865 | CTCCTCCTGCGGGAG[A/G]ACGGGTCAGCTCTTG | 16897 |
rs226833000 | snp | A/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60711186 | GGTGTTTCTGACCAG[A/T]GGGTTGAGGCCACAC | 16897 |
rs226872237 | snp | G/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60708933 | ATGTGGTTGGCCTGC[G/T]GTCTCCAGATGTGGC | 16897 |
rs227409461 | snp | A/C | | | missense | Llgl1 | GRCm38.p3 | 11:60713037 | TATGTGAAGGATTTT[A/C]TGGGGTGAGGCCAGC | 16897 |
rs227455318 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60711878 | GCCATCTGCTGGATG[A/G]CTGGTTAAGTGAGTG | 16897 |
rs227492544 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703603 | GGCTGGAGGGGATGT[C/T]CTTCCCTCTGTTGTG | 16897 |
rs227529241 | snp | G/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60701880 | GCATTGGGTGGGCCT[G/T]GAGCAGGGTGTGGGA | 16897 |
rs227878829 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60708316 | GATTTCTGGGTACCC[A/G]TTGCTCCTCTCTGCC | 16897 |
rs228051256 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60707655 | GCTCACTGGGTAGGT[A/G]TGGGTGGCAGACAGG | 16897 |
rs228501420 | in-del | -/GC | | | upstream-variant-2KB, utr-variant-5-prime | Llgl1 | GRCm38.p3 | 11:60699685 | CGGCGAGCCCGGGGG[-/GC]CCCCGTCCTCGCCCA | 16897 |
rs229123952 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60710639 | CCGTGGTGAGGCGGA[C/T]GGTGAGGGCCAGGAT | 16897 |
rs229188480 | in-del | -/TTT | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60697876 | TTCCTTTTCTTTTTC[-/TTT]TTTTTTTTTAAAGGC | 16897 |
rs229466909 | in-del | -/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703720 | GCTGTGACCTTGTAC[-/T]TGGGTTAGAGGTATC | 16897 |
rs230156669 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60709940 | CAGGAGAGCAGGAGT[A/G]CAGTGTAGCTCCATA | 16897 |
rs230628999 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700533 | CAGCTCCCACCTAGT[C/T]TGCACTGACCAGTAT | 16897 |
rs231096465 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703024 | CCTTTCGGAAATGAG[A/G]GGGTCTTTTGGTTGG | 16897 |
rs231152494 | snp | A/C | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60701717 | CTTTGGGGTGGGAGT[A/C]AGGTGAACTGGGATG | 16897 |
rs231525294 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60708757 | CTGGTCATAGCTCTG[C/T]ACTGCATCACCATCC | 16897 |
rs231548884 | snp | A/G | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60699326 | ATTGCCAGAATTAAA[A/G]TTATGCACAACCATC | 16897 |
rs231580284 | snp | A/C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60709410 | GTTCTGGGGCCACTC[A/C/T]GCCTCTCTCCTGCTG | 16897 |
rs231600915 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700399 | GTGCCTCAGTTTCCC[C/T]CGCCATGAAATGAGG | 16897 |
rs231665632 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60707750 | TCAGTGACTCAGTCT[C/T]AGTCCTAGTGAATCC | 16897 |
rs231886251 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60712735 | AGCGAGCTGGTGAGA[A/G]GGCACAGGGGTGGGG | 16897 |
rs231904393 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703900 | TAGCCATGAACTCCT[A/G]AGGTTGGGAAACTGA | 16897 |
rs231938667 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Llgl1, Flii | GRCm38.p3 | 11:60713909 | TTCTAACGCCTGGAC[C/T]GAGCTGGCCAGTCAT | 16897 |
rs232075705 | snp | C/T | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705435 | TTCTTGAGTTGGGAT[C/T]GGCTGGGCCATGGTT | 16897 |
rs232113921 | in-del | -/GGGGTGCGGGGGGGGGA | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60701625 | GTGGTCGGGGGGGGG[-/GGGGTGCGGGGGGGGGA]ACAGAAGGAATGCAG | 16897 |
rs232229528 | in-del | -/ACACACACACACACACACACAC | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703202 | AAAGAGTACATGTGT[-/ACACACACACACACACACACAC]ACACACACACACACA | 16897 |
rs232405953 | snp | C/T | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705194 | GACTGTGTTTCCCAC[C/T]GTGGGAGCCTTTAGT | 16897 |
rs232780099 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60709306 | ACAGACTCCAGGAGG[A/G]CAGAGGCCAGCATGT | 16897 |
rs232817672 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60707712 | TTTTCTGAGCATCCC[A/G]GATTCTTTGGGTGCT | 16897 |
rs232991827 | snp | A/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703475 | GTGCAGAGTCTGGCT[A/T]GAAGCAGCTTGGTAA | 16897 |
rs233209253 | snp | C/G | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705925 | CTGCCTTCCCCAGCA[C/G]GTAGATGGGCTCACC | 16897 |
rs233430002 | snp | C/T | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60698452 | AGCATGTCCTGAGCA[C/T]TTGCAAGGTTGAAAT | 16897 |
rs233704285 | snp | A/C | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60708715 | GCCTCTCCTCCCTCC[A/C]CCTGCCCCTCAGGGC | 16897 |
rs233808054 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60709127 | ACTTGAGTAAGGGTA[A/G]GGGAAGCACAGAGGC | 16897 |
rs234004193 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60701620 | ACAGTGTGGTCGGGG[A/G]GGGGGGGGTGCGGGG | 16897 |
rs234036822 | snp | G/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60710742 | AGGGACTCTGTGGGA[G/T]CACGTCCTCTCTGTG | 16897 |
rs234053610 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60701637 | GGGGGGGTGCGGGGG[A/G]GGGAACAGAAGGAAT | 16897 |
rs234067739 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60712519 | AATGGGTCCCTTAGC[C/T]GCCTTGGGCCCTGCA | 16897 |
rs234373264 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60710176 | TGACCCAGAGTGCTC[C/T]GGTCTGGTCAGGTGC | 16897 |
rs234444289 | snp | A/C | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705131 | AGTGGTATCCTTTGA[A/C]GATAGGGTTAGAGGT | 16897 |
rs234582623 | snp | A/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700302 | CTGCGCCTCCACTTT[A/T]CTCACCAGGCTCTGC | 16897 |
rs234951945 | in-del | -/GG | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60711849 | CTCATGGTGAAGCCT[-/GG]GCTGTTCTGTAGGCC | 16897 |
rs235271018 | snp | C/T | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60699651 | GCGCATGCGTGACTg[C/T]cccccccccccggcg | 16897 |
rs235541455 | in-del | -/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60701631 | GGGGGGGGGGGGTGC[-/G]GGGGGGGGGAACAGA | 16897 |
rs235698664 | in-del | -/TGGTTGGT | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60702165 | CCGAGCCAACTGCCG[-/TGGTTGGT]TGGTTGGTCGGTTGG | 16897 |
rs235804250 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60712350 | CAGTGTCCCTTAAAT[A/G]TTCCTTGGCCCTTTT | 16897 |
rs235809962 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703403 | TGGGGCAACAGGCTG[C/T]TGAATGTCTCCTTAC | 16897 |
rs235844780 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60702356 | ATTTATTTCTGAGAC[A/G]TCATCACATCATGTG | 16897 |
rs235914204 | snp | A/C | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703962 | CCTCCCTTCCCCCTG[A/C]AGGGCAGTCTCATCT | 16897 |
rs236022112 | in-del | -/CCCCAGCCCTTCTGATTACTGCCCT | | | utr-variant-3-prime, intron-variant | Llgl1 | GRCm38.p3 | 11:60713098 | CTAGGGGTCTTCTTA[-/CCCCAGCCCTTCTGATTACTGCCCT]CCCCAGCTCTCCTGA | 16897 |
rs236096245 | in-del | -/C | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703844 | ATGAGGAAGCCAAAG[-/C]CTAGATCCTCCTTCT | 16897 |
rs236113416 | in-del | -/GCGA | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60711268 | ATGGTTACAGTGAGG[-/GCGA]GTGAGGGAGAAGGGT | 16897 |
rs236168683 | snp | A/C | | | downstream-variant-500B, utr-variant-3-prime | Llgl1, Flii | GRCm38.p3 | 11:60714249 | GCTTGCAGGCTGTGG[A/C]TAGCTGAAGCAGGTA | 16897 |
rs236320275 | snp | C/T | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60697819 | AGCATCCTGTATTCC[C/T]GTGTTCCTTACTGCT | 16897 |
rs237498424 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60711139 | CCCCTTGAAGATGCC[C/T]TCAAGGTGACTCGTG | 16897 |
rs237770509 | snp | C/T | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60698132 | GGTTTCTCTGTGTAG[C/T]CTTGGCTGTCCTGGA | 16897 |
rs237784937 | snp | C/T | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60697957 | CACTGTGTCTTCAGG[C/T]ACACCAAAAGAGGAC | 16897 |
rs237813975 | snp | A/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700172 | GGCCTCTTTTCTTTC[A/T]TTTTTGGTGTGTAGC | 16897 |
rs237943308 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60708193 | TACTTTTGTCTCCTC[C/T]TCTTCCTCTCCCTAC | 16897 |
rs237971566 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60707560 | CTAACTTTAAGCTCC[C/T]GTCTTTGTTGTCTTT | 16897 |
rs238107021 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60702277 | ACTGCTTGTGTAGAC[C/T]CTGCCACCCCACCTC | 16897 |
rs238169651 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703320 | TGCCCCCATCTGGAC[A/G]CCGATGCCATACAAT | 16897 |
rs238333509 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60711323 | GCCTTCCTACTTTAC[A/G]TGTTCTTCACAGCGA | 16897 |
rs238370951 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60710502 | GTACTGGGGGGAGGC[A/G]GTGTGAGAAGCAGCT | 16897 |
rs238385395 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700937 | ATAACTAAAGAGCTG[C/T]CAGGAGAGGCTTCTC | 16897 |
rs238400071 | snp | G/T | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60706394 | TCCTCTTCCAGGCCC[G/T]TGTCCACACCTGCTG | 16897 |
rs239176661 | in-del | -/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700240 | TTTCTTTAACTCTTA[-/G]GCGGGCGAGAGAGGG | 16897 |
rs239280840 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60711203 | GGTTGAGGCCACACA[A/G]CAAGTGTAGACTGGG | 16897 |
rs239709378 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60704467 | GGTTTGAGTCATTGG[C/T]CTGCTGTACAGATGA | 16897 |
rs239879422 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703800 | TGCTTAGAGCTGTCC[C/T]TGTGGGTATTGCCCT | 16897 |
rs239879710 | snp | C/T | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60704643 | CCTAGCTTGTCTGCA[C/T]GTTTGTTCTTGACAA | 16897 |
rs239914627 | snp | A/C | | | downstream-variant-500B, intron-variant | Llgl1, Flii | GRCm38.p3 | 11:60714539 | TATCCAGGATGAGGG[A/C]GGGACAAGTGGCTCC | 16897 |
rs239945108 | snp | G/T | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60699087 | GCTCCTGTTCAGCCC[G/T]ACGTGCCTGCCACCT | 16897 |
rs239996082 | in-del | -/C | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60704786 | CTAGCACCAGGTGGT[-/C]CCCACCCCCGTGCTC | 16897 |
rs240092006 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60712318 | AGAAAACCCGGGCCA[C/T]CAAGGGTTGGCGGTG | 16897 |
rs240154770 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60707437 | GGTGTCTTGTGTCCC[A/G]GGAGGGGTGGTGAGG | 16897 |
rs240215409 | snp | C/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60708128 | CTAGTTCCTTTCTGA[C/G]TGACTTGGGAGCCCA | 16897 |
rs240224966 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60707842 | TTCCTCTTGGCCTGG[A/G]ACTGAGTTCCAGCCC | 16897 |
rs240282084 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60709022 | CCAATGTGGGCGGTA[A/G]GTCAGAGTGGGAACG | 16897 |
rs240435008 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700000 | GCCGCCTCTGCCCTG[C/T]GAGCGCCGCGCTGCT | 16897 |
rs240984255 | snp | A/G | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705493 | GCTTGGTGAGGTGCT[A/G]GCTGGATGCCTGGCT | 16897 |
rs241168695 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60712821 | CACTGAGCCAGGGCT[A/G]GAGGGCGCCTGTGTG | 16897 |
rs241548438 | in-del | -/A | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700686 | AAAAAACAAACAAAC[-/A]AAACAAAAAAAAAAA | 16897 |
rs241901884 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60710218 | TAGGGTGAAGGGATC[C/T]TGCTGGACACGGGGC | 16897 |
rs242151431 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60701371 | TACCTCCTTGGTACC[A/G]GGGCATGGCGGACAA | 16897 |
rs242155707 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60712914 | TGAGCAGCACTTCTT[C/T]CAACAGATACCATGG | 16897 |
rs242280258 | in-del | -/TC | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60699222 | AAGGAATTGAGATTT[-/TC]TTTTTTTTTTTTGAG | 16897 |
rs242310196 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60708208 | CTCTTCCTCTCCCTA[C/T]TTTCTCCTCGTTTGA | 16897 |
rs242468353 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703119 | CCTACCAATTCTTAG[A/G]TAATCCTACCATCAT | 16897 |
rs242621026 | in-del | -/TTTCCCCC | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700419 | ATGAAATGAGGCCAG[-/TTTCCCCC]TTGTGGATTCTGGAT | 16897 |
rs242744161 | in-del | -/CTGT | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60711982 | AGGACTAAGCTGGGC[-/CTGT]CTGTCTGTCAACAGG | 16897 |
rs242807088 | in-del | -/ACACACACACACACACACAC | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703203 | AAAGAGTACATGTGT[-/ACACACACACACACACACAC]ACACACACACAAATA | 16897 |
rs243016076 | snp | C/T | | | synonymous-codon | Llgl1 | GRCm38.p3 | 11:60708556 | CAGCCATGAGGATGG[C/T]ACTGTGCGGTTCTGG | 16897 |
rs243165875 | in-del | -/AGGGT | | | upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705471 | TCGGGAGGGTTCTCC[-/AGGGT]AGGCTTGGTGAGGTG | 16897 |
rs243188734 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60710154 | GCTGGCAGCCATGTC[C/T]GTGCCCTGACCCAGA | 16897 |
rs243228878 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700593 | ACTGGTGGGGCTCTG[A/G]TTAGATGTTACTTTT | 16897 |
rs243267103 | snp | A/C | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700690 | AAACAAACAAACAAA[A/C]AAAAAAAAAAAAACT | 16897 |
rs243604130 | snp | C/T | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705256 | ACCCAACTCCTTAGA[C/T]CTTTAGGCTGGCACA | 16897 |
rs243788861 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60711783 | CCGTGAGAGTACTAG[A/G]CATAGGACAAATGCA | 16897 |
rs243929941 | snp | A/G | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60697712 | CCTGCATTTTCACTT[A/G]CATGCCAGAAGAGGG | 16897 |
rs244078090 | snp | C/T | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60698759 | GGGCGGGTTGAGCAA[C/T]GCTGGTCGTGGGCAG | 16897 |
rs244244744 | snp | A/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60708417 | TGTGTGTAGCCTGAG[A/T]ACCTATTCTTCCTGC | 16897 |
rs244532806 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60701180 | TCATCTTGGGGAACG[A/G]GTTTGATTGCCACAG | 16897 |
rs245222959 | snp | C/T | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60698674 | AGATCAGGAGGGGCC[C/T]TTTGCTGTCTAGCCA | 16897 |
rs245702477 | snp | C/T | | | upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60699653 | GCATGCGTGACTgcc[C/T]cccccccccggcgag | 16897 |
rs245763183 | snp | A/G | | | utr-variant-3-prime, intron-variant | Llgl1 | GRCm38.p3 | 11:60713085 | ATCCCCAGGGCAACT[A/G]GGGGTCTTCTTACCC | 16897 |
rs245905220 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703657 | AGTTACCAAGATGAG[C/T]GCTGCTTGCCATTCG | 16897 |
rs246074400 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700262 | GAGAGAGGGAAAAGT[A/G]GGGGGTGGGGGGGCT | 16897 |
rs246097842 | snp | A/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60710830 | AGTGTGTAGTCCCTC[A/T]TATACTTGAGCTACC | 16897 |
rs246215662 | in-del | -/C | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705393 | GGTTACTGGTGTGTA[-/C]CCCCCATATTTGACC | 16897 |
rs246270061 | snp | A/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60708332 | TTGCTCCTCTCTGCC[A/T]ATTCCTGGTTGTCAA | 16897 |
rs246401867 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60704295 | TGACCATGGTCAAGA[A/G]TTGTTTGATCTGGCA | 16897 |
rs246969820 | in-del | -/CC | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60699651 | GCGCATGCGTGACTG[-/CC]CCCCCCCCCCGGCGA | 16897 |
rs247000556 | in-del | -/C | | | utr-variant-3-prime, intron-variant | Llgl1 | GRCm38.p3 | 11:60713118 | CCCTTCTGATTACTG[-/C]CCCTCCCCAGCTCTC | 16897 |
rs247095964 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60702026 | GGTGGTGCCCACTAA[A/G]GACTGTGGGGACTTA | 16897 |
rs247412074 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60709826 | TGCAGAAGCAGGCTG[A/G]TTGGGAAAGCCCTTG | 16897 |
rs247962134 | in-del | -/CTGGT | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60698760 | GCGGGTTGAGCAACG[-/CTGGT]CTGGTCGTGGGCAGT | 16897 |
rs248183077 | snp | C/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60707667 | GGTATGGGTGGCAGA[C/G]AGGGCCCAGCACCTA | 16897 |
rs248414339 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700060 | CGCCCCGCGCCGTGC[C/T]GTGCGCTTTCGGGCT | 16897 |
rs248584996 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60708265 | CAAGGCACCCTTAGG[C/T]TTCTTGCCTGACCTG | 16897 |
rs248661363 | in-del | -/CC | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700460 | TTGCGACCCGGCCAG[-/CC]TTCCTGACCTTACTA | 16897 |
rs248835886 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703550 | GGGTGGGAATGTGGC[C/T]CGTGGTTTATGAGGT | 16897 |
rs248961184 | snp | C/T | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60698134 | TTTCTCTGTGTAGCC[C/T]TGGCTGTCCTGGAAC | 16897 |
rs249376037 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60712745 | TGAGAGGGCACAGGG[A/G]TGGGGCAGGCAGGCA | 16897 |
rs249460010 | snp | A/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703776 | TTGCCCATGGTCTAC[A/T]CTGCCAGGTGCTTAG | 16897 |
rs249501331 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703905 | ATGAACTCCTGAGGT[C/T]GGGAAACTGAGGCTG | 16897 |
rs249517929 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60709071 | GCAGGGGTGAGGACA[A/G]ATGCAAAGTGTGGGG | 16897 |
rs249593674 | snp | C/T | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705950 | CTCACCTTACTCTCT[C/T]TTCCTCTTTCCTGCA | 16897 |
rs249820166 | in-del | -/GG | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60707507 | GGGAGATGGGTATGC[-/GG]GAGGCATGTGGCCAG | 16897 |
rs249858301 | snp | A/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60701829 | GTAGGACTGGCTGGC[A/T]GGTTTCCACCGGTGA | 16897 |
rs250063998 | snp | A/C | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60710700 | AGGTCGGGGACAGAT[A/C]AGGCAGAGCTGGTGC | 16897 |
rs250439510 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60707797 | GTTAGGAAGCCTCCC[C/T]TGATTCTGGCTCAAA | 16897 |
rs250656593 | in-del | -/TT | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60697877 | TTCCTTTTCTTTTTC[-/TT]TTTTTTTAAAGGCGT | 16897 |
rs251230974 | in-del | -/C | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705051 | TATGAGCCTGCTCTG[-/C]TGAAGCAGTGCAGAC | 16897 |
rs251256892 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60708175 | TGTCCCAGTGCTTCA[C/T]CTTACTTTTGTCTCC | 16897 |
rs251351202 | snp | C/T | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60699223 | AGGAATTGAGATTTT[C/T]TTTTTTTTTTTTGAG | 16897 |
rs251423612 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60708732 | CTGCCCCTCAGGGCC[A/G]GCCTTTGAGCTGGTC | 16897 |
rs251633217 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60711223 | TGTAGACTGGGAGGG[C/T]GCACTGGTCCCTGCA | 16897 |
rs251786773 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60712543 | CCCTGCACTCCCCTG[A/G]TGTTAGTGCCCATTT | 16897 |
rs251835902 | snp | G/T | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60698351 | TTTTGTGACTGCAGT[G/T]TAAAATTTCTGGGGA | 16897 |
rs251887543 | snp | C/G/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60708932 | GATGTGGTTGGCCTG[C/G/T]GGTCTCCAGATGTGG | 16897 |
rs252229842 | in-del | -/T | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60697756 | TATAGACATAGATGG[-/T]TTTGAGCAGCCAAAT | 16897 |
rs252317294 | snp | A/G | | | missense | Llgl1 | GRCm38.p3 | 11:60709594 | GGATTCCAGCCCCGC[A/G]TGCTGATACAGTGCC | 16897 |
rs252399839 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60701641 | GGGTGCGGGGGGGGG[A/G]ACAGAAGGAATGCAG | 16897 |
rs252431072 | snp | A/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700857 | GGGGGAGACCCTGCC[A/T]TGGCTCAGTTTTTTC | 16897 |
rs252844524 | snp | C/T | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705507 | TGGCTGGATGCCTGG[C/T]TGTGCATAGCAGGCC | 16897 |
rs252894041 | in-del | -/A | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705602 | GCCCACAGGTTAGTT[-/A]TTTCCTGGCCTGGCC | 16897 |
rs253107791 | snp | A/C | | | synonymous-codon | Llgl1 | GRCm38.p3 | 11:60712431 | CTCACTGAGTGCTCG[A/C]AACATCACAGAACCA | 16897 |
rs253538548 | snp | C/G | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705163 | TGGCCAGCTGAGACT[C/G]AGGCCAGTGGGCAGA | 16897 |
rs253579967 | snp | A/C | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700306 | GCCTCCACTTTTCTC[A/C]CCAGGCTCTGCCCTA | 16897 |
rs254071839 | snp | G/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60702466 | ATATTTGACACCTCA[G/T]GAAGGTATTCATGTC | 16897 |
rs254433201 | snp | C/T | | | synonymous-codon | Llgl1 | GRCm38.p3 | 11:60710002 | CCTTCACCCCAATGA[C/T]TCTTTGGCCATGGAG | 16897 |
rs254506146 | in-del | -/AC | | | downstream-variant-500B, utr-variant-3-prime | Llgl1, Flii | GRCm38.p3 | 11:60714204 | TCTGCACACATGTGG[-/AC]ACACTGGTGGGGCTT | 16897 |
rs254523215 | snp | A/G | | | missense, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60706312 | TACTGGTCATCTGGA[A/G]CCAGGCCACACAGTC | 16897 |
rs254848084 | snp | C/T | | | synonymous-codon | Llgl1 | GRCm38.p3 | 11:60707646 | TGGGCTGCTGCTCAC[C/T]GGGTAGGTATGGGTG | 16897 |
rs255220082 | snp | A/C | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60710576 | GCCTGTATAGCACAT[A/C]TAGGAGACATGTTTG | 16897 |
rs255401945 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60701215 | TGTTAGGAGATCTCT[A/G]GAGAATAGTGAGCCC | 16897 |
rs255403324 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60711329 | CTACTTTACGTGTTC[C/T]TCACAGCGACCCACC | 16897 |
rs255626294 | in-del | -/GG | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60701616 | CTGCACAGTGTGGTC[-/GG]GGGGGGGGGGGTGCG | 16897 |
rs255765446 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60711179 | CTGGGCTGGTGTTTC[C/T]GACCAGTGGGTTGAG | 16897 |
rs255813907 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700978 | CTCTTTTTGGCTCAC[C/T]GTGAGGGTGTGCCCC | 16897 |
rs255848590 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700198 | GTAGCCCGGCTCGGC[C/T]GAGGGACATTCAGGG | 16897 |
rs255907166 | in-del | -/C | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60701266 | TGTAGTCCAGGGTGA[-/C]CAGTGGGTATTGGGT | 16897 |
rs256133879 | in-del | -/GCCTCTG | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60710263 | AGAGCACGTCTGAGC[-/GCCTCTG]GCCTCTGGCCCTCCC | 16897 |
rs256320682 | snp | C/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60709412 | TCTGGGGCCACTCAG[C/G]CTCTCTCCTGCTGTG | 16897 |
rs256918082 | in-del | -/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700670 | TTTCCATTACACACG[-/T]TAAAAAACAAACAAA | 16897 |
rs257319274 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60707506 | CGGGAGATGGGTATG[C/T]GGGAGGCATGTGGCC | 16897 |
rs257459259 | in-del | -/AC | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700693 | AAACAAACAAACAAA[-/AC]AAAAAAAAAACTGAG | 16897 |
rs257489591 | in-del | -/TGA | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60701091 | ATGGCTTCCCCTGAC[-/TGA]TGATGCTACAGTGGG | 16897 |
rs257595418 | snp | A/C | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703678 | TTGCCATTCGAAGAC[A/C]CGTGGATGCTATGCT | 16897 |
rs257688212 | snp | C/T | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705952 | CACCTTACTCTCTCT[C/T]CCTCTTTCCTGCAGT | 16897 |
rs257753377 | snp | A/G | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60704648 | CTTGTCTGCACGTTT[A/G]TTCTTGACAAGTTAC | 16897 |
rs257761111 | snp | A/C | | | missense | Llgl1 | GRCm38.p3 | 11:60710334 | GACCTGCCCACACGA[A/C]CTGGAGATGACACCC | 16897 |
rs257896416 | in-del | -/CTTGAAGTGGTATC | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705111 | CTGGATAGAACCCTT[-/CTTGAAGTGGTATC]CTTTGAAGATAGGGT | 16897 |
rs258126453 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60709846 | GAAAGCCCTTGTAAA[C/T]GCTCTCCTCCTGCGG | 16897 |
rs258155473 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60709048 | GAACGGAACACCAGG[A/G]AAGGTTGGCAGGGGT | 16897 |
rs258171229 | in-del | -/TCTCTT | | | downstream-variant-500B, intron-variant | Llgl1, Flii | GRCm38.p3 | 11:60714582 | CTGGCTTCAGTAATC[-/TCTCTT]TCTTACCTGGCAAGC | 16897 |
rs258551809 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703812 | TCCTTGTGGGTATTG[C/T]CCTCGTGCTTAGTAT | 16897 |
rs258564517 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700079 | CGCTTTCGGGCTCCT[A/G]GTCTCTGAACCCCTG | 16897 |
rs258600221 | snp | A/G | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60698587 | CCTCTGTGCATCTGG[A/G]GTGATATCACTTTAA | 16897 |
rs258929937 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703671 | GTGCTGCTTGCCATT[C/T]GAAGACCCGTGGATG | 16897 |
rs259187532 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703154 | GCAGCTGTGACTGGG[A/G]CAGTTAGGGGTGGCC | 16897 |
rs259204820 | snp | G/T | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60698872 | GAGGACAGGGGCTTG[G/T]CCCGCTTAAACTCCT | 16897 |
rs259284443 | snp | C/T | | | synonymous-codon, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60704720 | TCGGGACGCAGCCAC[C/T]GTCACCCAGATGCAT | 16897 |
rs259392049 | snp | A/G/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60701629 | TCGGGGGGGGGGGGG[A/G/T]GCGGGGGGGGGAACA | 16897 |
rs259527649 | in-del | -/A | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60698244 | CCACCACTGCCCGGT[-/A]AAAAGTCATTCTTAT | 16897 |
rs259887179 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60707668 | GTATGGGTGGCAGAC[A/G]GGGCCCAGCACCTAG | 16897 |
rs259974620 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60711874 | GTAGGCCATCTGCTG[A/G]ATGGCTGGTTAAGTG | 16897 |
rs260134737 | snp | A/G | | | missense | Llgl1 | GRCm38.p3 | 11:60712944 | GAACCACCCGAGGCC[A/G]CTCTCTCGCCTGTGT | 16897 |
rs260260675 | snp | A/T | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60697828 | TATTCCTGTGTTCCT[A/T]ACTGCTGAGCCATCT | 16897 |
rs260297672 | snp | A/C | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700729 | GTAGGGAGAGGGCCG[A/C]TTATCTTTCCTTGCC | 16897 |
rs260503986 | in-del | -/TC | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60697880 | TTTTCTTTTTCTTTT[-/TC]TTTTTAAAGGCGTGT | 16897 |
rs260551811 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60710155 | CTGGCAGCCATGTCC[A/G]TGCCCTGACCCAGAG | 16897 |
rs260618947 | in-del | -/AG | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60710809 | ATACTAAGTATAAAC[-/AG]AAAATAGTGTGTAGT | 16897 |
rs260732117 | snp | G/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60710220 | GGGTGAAGGGATCCT[G/T]CTGGACACGGGGCAG | 16897 |
rs260862318 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60704234 | CATCTGGAAGCTGAG[C/T]AGTGGAAGCTGTTGG | 16897 |
rs261047377 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60706915 | CCAGCATGTGCCCTG[C/T]ACTCCCGGAGCTCCT | 16897 |
rs261229977 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60709792 | GGTGGTCTGGGATTC[C/T]GTTTCCTTTCAGAGG | 16897 |
rs261808515 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Llgl1, Flii | GRCm38.p3 | 11:60713913 | AACGCCTGGACTGAG[C/T]TGGCCAGTCATTTCT | 16897 |
rs262117229 | in-del | -/CA | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705949 | CTCACCTTACTCTCT[-/CA]CTTCCTCTTTCCTGC | 16897 |
rs262175925 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60708207 | CCTCTTCCTCTCCCT[A/G]CTTTCTCCTCGTTTG | 16897 |
rs262523748 | in-del | -/C | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60708256 | CTTACCTGCAAGGCA[-/C]CCCTTAGGCTTCTTG | 16897 |
rs262997680 | snp | C/T | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60698033 | AGACCTCTGGAAGAG[C/T]AGTCAGTGCTCTTAA | 16897 |
rs263115672 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703566 | CGTGGTTTATGAGGT[A/G]ATGTCCCTTGTCAGG | 16897 |
rs263238384 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60702043 | ACTGTGGGGACTTAC[C/T]GTGCTGTCGTGTTCT | 16897 |
rs263842749 | snp | A/C | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60708527 | GGGGCAGGCTCTGAC[A/C]CTCACCTTCTCTACA | 16897 |
rs263977470 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700045 | TGGGGTGTCGGGCTG[C/T]GCCCCGCGCCGTGCC | 16897 |
rs264010135 | snp | A/G | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705471 | TCGGGAGGGTTCTCC[A/G]GGGTAGGCTTGGTGA | 16897 |
rs264134355 | snp | C/T | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60698838 | TAAGGGTCAACGCCT[C/T]CTCTCTTGACAAAGA | 16897 |
rs264229073 | snp | A/T | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60698394 | GTAACCTAATAAACT[A/T]TTACTGCAGAGATGA | 16897 |
rs264315839 | snp | G/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60707962 | GAAACGCCAGGCTAG[G/T]TCAGGGCACTGGTGA | 16897 |
rs264349954 | snp | G/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60702369 | ACGTCATCACATCAT[G/T]TGGTCCATGCTGTCC | 16897 |
rs264368264 | snp | A/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60711793 | ACTAGGCATAGGACA[A/T]ATGCATATGTCCAGT | 16897 |
rs264493775 | snp | A/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60709119 | GTGCCATGACTTGAG[A/T]AAGGGTAGGGGAAGC | 16897 |
rs264895635 | in-del | -/CTCT | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60707818 | TGGCTCAAAGCCCTC[-/CTCT]CTCTCCACTTCCTCT | 16897 |
rs265086201 | snp | A/G | | | downstream-variant-500B, intron-variant | Llgl1, Flii | GRCm38.p3 | 11:60714661 | CATGTAGACCTGAGG[A/G]TACAGAGGATGAAAT | 16897 |
rs265224592 | in-del | -/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60710900 | TGTGTTTATTGCTTG[-/T]TTTTTTAGACAGGGA | 16897 |
rs265344141 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705879 | AATGCAGAGAGGCAT[-/AA]GAGAGCCCATAGAAA | 16897 |
rs265463390 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60704332 | TGTTCTGCTTAGGCC[C/T]GTTAACCTCTACTGC | 16897 |
rs265790187 | snp | A/C | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700076 | GTGCGCTTTCGGGCT[A/C]CTGGTCTCTGAACCC | 16897 |
rs266140953 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703434 | TCTGGAAATAGCACC[C/T]TAACCTGCCTTCAGG | 16897 |
rs387002976 | in-del | -/TCTCCCCCC | | | upstream-variant-2KB | Llgl1 | Mm_Celera | 11:60699650 | GCGCATGCGTGACTG[-/TCTCCCCCC]CCCCCCCCCCCCGGC | 16897 |
rs387041507 | in-del | -/CACACACA | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703226 | ACACACACACACACA[-/CACACACA]AATACGAAGACCCCA | 16897 |
rs387623050 | snp | A/C | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700678 | ACACACGTTAAAAAA[A/C]AAACAAACAAACAAA | 16897 |
rs387829157 | in-del | -/A | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700703 | AACAAAAAAAAAAAA[-/A]CTGAGGTTCAGTAGG | 16897 |
rs578776456 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60701621 | CAGTGTGGTCGGGGG[A/G]GGGGGGGTGCGGGGG | 16897 |
rs578817478 | snp | G/T | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705380 | TCTTCCAAGTGTAGG[G/T]TTACTGGTGTGTACC | 16897 |
rs578991671 | snp | C/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60711846 | AGGCTCATGGTGAAG[C/G]CTGGGCTGTTCTGTA | 16897 |
rs580778792 | snp | A/G | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60704796 | GGTGGTCCCACCCCC[A/G]TGCTCTCCTCCCCTT | 16897 |
rs581082402 | snp | G/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60708898 | CTGCAGGCCAGGTGC[G/T]GTTGGCCTGCAGTCT | 16897 |
rs581601175 | snp | A/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700461 | TTGCGACCCGGCCAG[A/T]TCCTGACCTTACTAA | 16897 |
rs581802500 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60701645 | GCGGGGGGGGGAACA[A/G]AAGGAATGCAGAGGA | 16897 |
rs582657073 | snp | A/T | | | upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60697769 | GGTTTTGAGCAGCCA[A/T]ATGGTTACTTGCAAT | 16897 |
rs582849828 | snp | A/G | | | upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60698531 | CTGATCATGACTTGT[A/G]TGGGGCTGATCTTGG | 16897 |
rs583870595 | snp | A/C | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700686 | TAAAAAACAAACAAA[A/C]AAACAAAAAAAAAAA | 16897 |
rs584081237 | snp | A/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60703194 | TGATGAGAGAAAGAG[A/T]ACATGTGTACACACA | 16897 |
rs584998938 | snp | G/T | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60705603 | GCCCACAGGTTAGTT[G/T]TTCCTGGCCTGGCCT | 16897 |
rs585048518 | snp | C/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60708939 | TTGGCCTGCGGTCTC[C/T]AGATGTGGCTATTGG | 16897 |
rs586045393 | snp | A/T | | | upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60698093 | AGTCATTCTTTTTTG[A/T]TGTTGTTTTGTTTTT | 16897 |
rs586773618 | snp | A/T | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60710814 | TAAGTATAAACAAAA[A/T]AGTGTGTAGTCCCTC | 16897 |
rs587005583 | snp | C/T | | | intron-variant, upstream-variant-2KB | Llgl1 | GRCm38.p3 | 11:60704773 | GCTCCCCTCCTTTAC[C/T]AGCACCAGGTGGTCC | 16897 |
rs587009316 | snp | A/G | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700466 | ACCCGGCCAGTTCCT[A/G]ACCTTACTAAAGTTG | 16897 |
rs587319055 | snp | A/C | | | intron-variant | Llgl1 | GRCm38.p3 | 11:60700698 | AAACAAACAAAAAAA[A/C]AAAAACTGAGGTTCA | 16897 |
rs864269556 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Llgl1, Flii | GRCm38.p3 | 11:60714089 | CTGTAGATGCCACCT[C/T]CGGCTTTTCTGTCTT | 16897 |