SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4230848 | snp | A/G | 0.48 | 0.0979796 | utr-variant-3-prime, nc-transcript-variant | Gga1, LOC102632079 | GRCm38.p3 | 15:78894585 | GACAAGAGCAGCTAA[A/G]CCAGGAAAAAAGTCA | 106039 |
rs4230849 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime, nc-transcript-variant | Gga1, LOC102632079 | GRCm38.p3 | 15:78894514 | CCTACTTGACCACAG[A/G]AGGGTGGGCAGATGT | 106039 |
rs4230850 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime, nc-transcript-variant | Gga1, LOC102632079 | GRCm38.p3 | 15:78894492 | GGCAGATGTGAGGTG[C/T]TCCCGGGAGGCCCCA | 106039 |
rs4230851 | snp | C/G | 0.32 | 0.24 | utr-variant-3-prime, nc-transcript-variant | Gga1, LOC102632079 | GRCm38.p3 | 15:78894431 | GGGAGTTCCATGGCC[C/G]TCCAGGGGGCATGTC | 106039 |
rs4230852 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime, nc-transcript-variant | Gga1, LOC102632079 | GRCm38.p3 | 15:78894335 | GCCCCGGGGGCTGAG[C/T]GGAGAGCTCCTTCAG | 106039 |
rs13461022 | snp | G/T | 0.48 | 0.0979796 | utr-variant-3-prime, downstream-variant-500B | Gga1, LOC102632079 | GRCm38.p3 | 15:78894168 | AGGCCCAGCCATAAC[G/T]TGGAGGCCATGCTGG | 106039 |
rs13461023 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Gga1, LOC102632079 | GRCm38.p3 | 15:78894041 | GGAGCAGGGAGGGGC[C/T]GTATGCCCTGGAAGG | 106039 |
rs31566767 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Gga1 | Mm_Celera | 15:78885052 | AAGGAACTACTGTTT[A/G]CAAGTTATATATATT | 106039 |
rs31566769 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Gga1 | Mm_Celera | 15:78885445 | TGTGGAGGTGGCATC[C/T]TGTGTGGAGCCGGCT | 106039 |
rs31566771 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Gga1 | Mm_Celera | 15:78886027 | TGTGCGTGTGTGTAC[A/G]TATGATGTCCTATAG | 106039 |
rs31566773 | snp | G/T | 0.32 | 0.24 | intron-variant | Gga1 | Mm_Celera | 15:78886099 | GCTCAGAGGCTGATA[G/T]TTAGAGGGAAGTAGC | 106039 |
rs31567695 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Gga1 | Mm_Celera | 15:78887249 | TGACCGCAGGAAAAG[A/G]AACGATCAAGGCCAC | 106039 |
rs31567697 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Gga1 | Mm_Celera | 15:78887390 | GAAATCTCCCAGCTC[A/G]CTAATGACAGCAGCA | 106039 |
rs31567699 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Gga1 | Mm_Celera | 15:78887427 | CTTTCCACGTTTTAA[A/T]AGTGTGTGCCCCACC | 106039 |
rs31567701 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Gga1 | Mm_Celera | 15:78887626 | ATGTGAGGCTGCCAA[A/G]CACAAGCCTACCTCC | 106039 |
rs31567703 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Gga1 | Mm_Celera | 15:78888155 | GCGGGTGAATGCCAT[C/T]GAGGAGGTCAACAAC | 106039 |
rs31568525 | snp | C/T | 0.32 | 0.24 | intron-variant | Gga1 | GRCm38.p3 | 15:78888687 | TCCTGTGCAGGCATC[C/T]TATCTGCCCAGGAGG | 106039 |
rs31568527 | snp | A/G | 0.32 | 0.24 | intron-variant | Gga1 | GRCm38.p3 | 15:78888761 | TCACAGCCCCAGTGT[A/G]TCACATCACCCCTTC | 106039 |
rs31568529 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Gga1 | GRCm38.p3 | 15:78889070 | GCAGCTGGTCCGGGG[C/T]GAGGAGGTCAACGGT | 106039 |
rs31568531 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Gga1 | GRCm38.p3 | 15:78889088 | GGAGGTCAACGGTGA[C/T]GCCACAGCCAGCTCC | 106039 |
rs31568533 | snp | A/G | 0.32 | 0.24 | intron-variant | Gga1 | GRCm38.p3 | 15:78889456 | TTTGGGTATGAGAGC[A/G]GCAGCCATATCTTAA | 106039 |
rs31569205 | snp | G/T | 0.32 | 0.24 | intron-variant | Gga1 | GRCm38.p3 | 15:78889564 | TAAGCAAAGCTGGTT[G/T]ATTGTGAACAAAAGA | 106039 |
rs31569207 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78889855 | CCTGCTTGATGACGA[A/G]CTCATGTCTCTGGGT | 106039 |
rs31569209 | snp | C/T | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78889984 | CGAGCAGCATGGCTT[C/T]CCTATTCTGGGTGAA | 106039 |
rs31569211 | snp | C/T | 0.495868 | 0.0452663 | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78891174 | CCTGCTCTTAGCTGC[C/T]GAGGGCCCAAGGTGA | 106039 |
rs31569213 | snp | A/G | 0.48 | 0.0979796 | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78891185 | CTGCCGAGGGCCCAA[A/G]GTGAAAGTTCCAACT | 106039 |
rs31569975 | snp | A/G | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78891249 | ACGGAGAGGAAGTTA[A/G]TGTGGGCTGCAAGGT | 106039 |
rs31569977 | snp | C/T | 0.489796 | 0.070696 | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78891271 | CTGCAAGGTGGCTGC[C/T]GGGATGATGCTTTCT | 106039 |
rs31569979 | snp | A/G | 0.473373 | 0.11227 | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78891588 | GAGAGGTGACAGGCA[A/G]GTGGGTCCTGGGACA | 106039 |
rs31569981 | snp | C/T | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78891604 | GTGGGTCCTGGGACA[C/T]GGCAGTACCATCCCA | 106039 |
rs31569983 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78891809 | TCTATTATCCTCTCT[A/G]CTGTACCTCTCTCAG | 106039 |
rs31570784 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon, downstream-variant-500B | Gga1, Mir6955 | GRCm38.p3 | 15:78892022 | AGCGGCCTGGACGAC[C/T]TGGACCTCTTGGGGA | 106039 |
rs31570786 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Gga1 | GRCm38.p3 | 15:78892428 | CCACTACAAAATCAC[G/T]TGCTAATACACTGTC | 106039 |
rs31570787 | snp | C/G | 0.32 | 0.24 | intron-variant | Gga1 | GRCm38.p3 | 15:78893036 | AGAATGCATGACCCA[C/G]ACTTTGAACAGAGCC | 106039 |
rs31570789 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Gga1 | GRCm38.p3 | 15:78893493 | TGGGAAGGGAGCTGC[C/T]TCTGCTGTGGTGGCT | 106039 |
rs31570790 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gga1 | GRCm38.p3 | 15:78893679 | CTGACGTGGCAGTGC[C/T]CCAGGGTGGCGCTAA | 106039 |
rs31570792 | snp | A/C | 0.124444 | 0.216185 | synonymous-codon, downstream-variant-500B | Gga1, LOC102632079 | GRCm38.p3 | 15:78893751 | GAAGGTTCGCCTCCG[A/C]TACAAGCTCATCTTC | 106039 |
rs31571784 | snp | A/C | 0.124444 | 0.216185 | utr-variant-3-prime, nc-transcript-variant | Gga1, LOC102632079 | GRCm38.p3 | 15:78894384 | GCTCTCAGGCTCCCA[A/C]GGGCCATGGAAACTT | 106039 |
rs31571785 | snp | C/T | 0.32 | 0.24 | downstream-variant-500B, nc-transcript-variant | Gga1, LOC102632079 | GRCm38.p3 | 15:78894586 | GACTTTTTTCCTGGA[C/T]TAGCTGCTCTTGTCA | 106039 |
rs31571786 | snp | G/T | 0.489796 | 0.070696 | downstream-variant-500B, nc-transcript-variant | Gga1, LOC102632079 | GRCm38.p3 | 15:78894827 | GGAGGTCTGGCTGCT[G/T]CAGAAGTCAAGGGGA | 106039 |
rs31571787 | snp | C/T | 0.244898 | 0.249948 | downstream-variant-500B, nc-transcript-variant | Gga1, LOC102632079 | GRCm38.p3 | 15:78894890 | GCAGCCGGTCTTGTG[C/T]TTCTCCCTGCCCGAC | 106039 |
rs31571789 | snp | C/T | 0.32 | 0.24 | downstream-variant-500B, nc-transcript-variant | Gga1, LOC102632079 | GRCm38.p3 | 15:78894914 | GCCCGACACACGGCT[C/T]TCTCCAAAGCCCTGC | 106039 |
rs31571791 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B, nc-transcript-variant | Gga1, LOC102632079 | GRCm38.p3 | 15:78894952 | CTACTCTTCACCCGG[C/T]GTGGTAAAAGGCTGG | 106039 |
rs45780045 | snp | G/T | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78875339 | ggcgggaagcagtgt[G/T]cattccacactctct | 106039 |
rs45792305 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78878607 | GGTTGATTGGTGGTT[A/G]GAAGGAGACAGTGAC | 106039 |
rs45938022 | snp | G/T | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78875718 | GTAGCTGGAGATGTC[G/T]CTCAGTTGGTAGCGT | 106039 |
rs45966445 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78893689 | AGTGCCCCAGGGTGG[C/T]GCTAACCTCCCTTCC | 106039 |
rs45987147 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879627 | CACCCACAAGGTTCC[C/T]GGGATAGATTGGTAC | 106039 |
rs46001773 | snp | A/T | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78876578 | TTCCCCATCACCTTG[A/T]GAGTGTTACGTGCTT | 106039 |
rs46005111 | snp | A/G | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78876985 | CTTCAGGACTGCCAG[A/G]GCAAGACAGTGAGCC | 106039 |
rs46144458 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879250 | GTGGGGTCATGTCTC[C/T]TCCAGTTCTAAGATC | 106039 |
rs46174362 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78892814 | AACCCTGACCCCCTC[A/G]TTCCCAGGGAGGGCA | 106039 |
rs46269678 | snp | A/G | | | intron-variant | Gga1 | Mm_Celera | 15:78885783 | GACCATTTCACAGAG[A/G]GGTCCCACACACAGT | 106039 |
rs46325074 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880884 | GCCCACTGATCCCAC[C/T]GGAAGGTCAGTGCTC | 106039 |
rs46431853 | snp | A/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78878920 | GCTCAGCCTGCTCTC[A/T]TATAGAACCAAGACT | 106039 |
rs46514386 | snp | C/T | | | synonymous-codon, downstream-variant-500B | Gga1, Mir6955 | GRCm38.p3 | 15:78892009 | TCCACCAACGAGCAG[C/T]GGCCTGGACGACCTG | 106039 |
rs46577148 | snp | G/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880761 | CAGCGTGAGAGATGG[G/T]AAAGTCAGCGTAGTG | 106039 |
rs46632470 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880967 | ACCCCTCTTAACTGC[A/G]CCAGTTGCAGGACAG | 106039 |
rs46779864 | snp | A/G | | | intron-variant | Gga1 | Mm_Celera | 15:78886404 | GGAAGGGAAGAATCA[A/G]TTTTCACAAGTGCCC | 106039 |
rs46783089 | snp | C/T | | | intron-variant | Gga1 | Mm_Celera | 15:78887707 | ATGCCTTTAAAGGCC[C/T]GGACCCACACACTGG | 106039 |
rs46945337 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78889144 | GGCTCTGGGGGGCCC[A/G]GGTGCGGGGCGGCAT | 106039 |
rs47156381 | snp | G/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78886672 | GATGTTAATATGTTT[G/T]TTTTTTTGTTTTTTT | 106039 |
rs47245797 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78882551 | CACCACTGCCCGACC[A/G]TAGGACACATGTTAA | 106039 |
rs47273124 | snp | A/G | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78876066 | GCGCCACCACTGCCC[A/G]GCCTGCAGTTGGGTT | 106039 |
rs47371218 | snp | C/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78881355 | TTACCGGGACATGAG[C/G]AGTCCTACACCTGGT | 106039 |
rs47379383 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880805 | GGAGGCCGTCCCTGG[A/G]TGTAGTCTCTGAGGA | 106039 |
rs47390346 | snp | G/T | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78875325 | GTGAGTGGAGAAAGG[G/T]CGGGAAGCAGTGTGC | 106039 |
rs47400003 | snp | C/T | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78876894 | GCGTGGTGGCACACT[C/T]CTTTAATGTCTGCAC | 106039 |
rs47449461 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78881264 | GGCTTCAGGGGTGCC[A/G]CCCCCTTGAGGGGAG | 106039 |
rs47739007 | snp | C/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78878508 | GAAGCCAGCCTCGAA[C/G]GAAGTTGAACTGGAA | 106039 |
rs47790171 | snp | A/G | | | intron-variant | Gga1 | Mm_Celera | 15:78884995 | GGATTAAAGGCGTGC[A/G]CCACCACCGCCCGGC | 106039 |
rs47896452 | snp | A/T | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78875961 | ggttttgttctgtgt[A/T]gccctgggtcctgga | 106039 |
rs47906703 | snp | C/T | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78875417 | CTTGATTTCTCCTCC[C/T]CTTGAATTGTGGGAA | 106039 |
rs48084533 | snp | C/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78878407 | CCCAGAGAAGCCTTC[C/G]GGTCTATCCTCAAGC | 106039 |
rs48189477 | snp | G/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879241 | GGGAAAGGGGTGGGG[G/T]CATGTCTCTTCCAGT | 106039 |
rs48231196 | snp | C/T | | | intron-variant | Gga1 | Mm_Celera | 15:78886335 | AGCAAGATGGCTCTA[C/T]AGGTATAGATATCCG | 106039 |
rs48329896 | snp | A/G | | | intron-variant | Gga1 | Mm_Celera | 15:78886755 | GATCAGGCTGGCCTC[A/G]AACTCAGAAATCTGC | 106039 |
rs48332840 | snp | A/C | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78876659 | TCTGATAAGTGCGGG[A/C]GTTATCATCACCTTG | 106039 |
rs48370797 | snp | G/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78882654 | AGACCACATAGGATC[G/T]GTAGACCCTGAACTT | 106039 |
rs48371264 | snp | C/T | | | intron-variant | Gga1 | Mm_Celera | 15:78886590 | GGTGGCTGTCCTCTG[C/T]ATCCCCCAAACATAT | 106039 |
rs48542079 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78893090 | GGCTCCAGGGTGGGC[A/G]TCCTGCCTCTAAGAG | 106039 |
rs48587971 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78884455 | ATGCTTGCCTAGCAT[A/G]CACGAAGCTCTGCCT | 106039 |
rs48771128 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78883975 | CAGCTCCACCAGGCC[C/T]CTTGCAGGGCCTATG | 106039 |
rs48802643 | snp | A/G | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78875682 | CAGCTTGGGCTATAA[A/G]GACTCTAGATGGAGG | 106039 |
rs49068853 | snp | A/T | | | downstream-variant-500B, nc-transcript-variant | Gga1, LOC102632079 | GRCm38.p3 | 15:78894829 | AGGTCTGGCTGCTGC[A/T]GAAGTCAAGGGGAAG | 106039 |
rs49069268 | snp | C/T | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78876589 | CTTGAGAGTGTTACG[C/T]GCTTTGAGATACGAT | 106039 |
rs49430977 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78882351 | TGATGGCAGGGATTC[C/T]TTAACTCACACACAA | 106039 |
rs49847499 | snp | G/T | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78875215 | TCGATGAGCTGCTGC[G/T]CGTGCCTCAGGAGGA | 106039 |
rs49960345 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78881567 | CCTGGGTGATAGAAC[A/G]CTCCGCACAGTGAGC | 106039 |
rs50036506 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78882033 | GGCATGTGCTTCACA[A/G]GGCCAGTAGAGGGCT | 106039 |
rs50263917 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880530 | CCTGAGCAGAGCGGC[C/T]CTCAGCCTGGGCAGC | 106039 |
rs50269545 | snp | C/T | | | intron-variant | Gga1 | Mm_Celera | 15:78886742 | AACTCACCCTGTAGA[C/T]CAGGCTGGCCTCGAA | 106039 |
rs50683809 | snp | A/C | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78875698 | GACTCTAGATGGAGG[A/C]AGAAGTAGCTGGAGA | 106039 |
rs51079585 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880920 | TGGGGGTGTCCAGCA[A/G]GAAGTGGAGGGAATC | 106039 |
rs51164168 | snp | A/G | | | intron-variant | Gga1 | Mm_Celera | 15:78886225 | AACTCCAGAGGCTGA[A/G]GCAGGAGGATCCTGA | 106039 |
rs51164886 | snp | C/T | | | intron-variant | Gga1 | Mm_Celera | 15:78886734 | TGTCCTGGAACTCAC[C/T]CTGTAGATCAGGCTG | 106039 |
rs51241765 | snp | A/G | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78875637 | CTGCCTAACATGTTT[A/G]TATGAAATGCTAGGT | 106039 |
rs51340145 | snp | C/T | | | intron-variant | Gga1 | Mm_Celera | 15:78885965 | GGCTGGCCTGGTGTA[C/T]AGGGGTAGAAGGGAT | 106039 |
rs51349120 | snp | C/T | | | intron-variant | Gga1 | Mm_Celera | 15:78886928 | CAGCACTTGGGAGGC[C/T]GAGGCAGGAGGAATT | 106039 |
rs51429961 | snp | A/T | | | intron-variant | Gga1 | Mm_Celera | 15:78887024 | TCTCAAGACAGAAAA[A/T]TTTCAAAAGGTGTTG | 106039 |
rs51608583 | snp | A/C | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879187 | GATGAGCCCCCCCCC[A/C]CACACACACACACAC | 106039 |
rs52066488 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78889676 | GTGCTCACCGCTGCT[C/T]CCAGTGCCCCCCAGG | 106039 |
rs52218493 | snp | A/G | | | intron-variant | Gga1 | Mm_Celera | 15:78886725 | AGCCCTGGCTGTCCT[A/G]GAACTCACCCTGTAG | 106039 |
rs52344236 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78888366 | CCCCAGCCCACCCCA[A/G]CCCACTCATAACCCA | 106039 |
rs108297680 | snp | A/G | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78876955 | ATTCCACGCCAGCCT[A/G]TTCTACAGAGCGAGC | 106039 |
rs108356651 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78889636 | CCTGTAATGAGATGG[A/G]AGGAGGAGGAGGAGG | 106039 |
rs108873047 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78889620 | CTGAGGGGCTAGGAG[A/G]CCTGTAATGAGATGG | 106039 |
rs211728780 | snp | A/C | | | intron-variant | Gga1 | GRCm38.p3 | 15:78883107 | CCAAGCCACGGAGGC[A/C]CTGTGGTCGAGCAAC | 106039 |
rs211886416 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78882125 | TCTATTCCTCCTACC[C/T]AGGCCTCCACTTGCC | 106039 |
rs212070930 | in-del | -/GA | | | intron-variant | Gga1 | GRCm38.p3 | 15:78893666 | TGAGGGCCCAGCTCT[-/GA]CGTGGCAGTGCCCCA | 106039 |
rs212120646 | snp | A/G | | | downstream-variant-500B, nc-transcript-variant | Gga1, LOC102632079 | GRCm38.p3 | 15:78894634 | AGGTAGGGAAGGTTC[A/G]GGAGGTGGGGGCCTA | 106039 |
rs212282174 | snp | G/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78893670 | GGCCCAGCTCTGACG[G/T]GGCAGTGCCCCAGGG | 106039 |
rs212340888 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78884519 | CCTATAATGCTAGCA[C/T]TTAGGTACTGGGGCA | 106039 |
rs212402995 | in-del | -/CCACAA | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879187 | ATGAGCCCCCCCCCC[-/CCACAA]CACACACACACACAC | 106039 |
rs212441009 | snp | A/T | | | intron-variant | Gga1 | Mm_Celera | 15:78885479 | TGCACTGACCCATGC[A/T]GGCATCTGCCTTCAG | 106039 |
rs212731146 | in-del | -/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78881256 | CTGCTGGGGGCTTCA[-/G]GGGTGCCGCCCCCTT | 106039 |
rs213004820 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78888713 | GGAGGGAGAACTCTC[C/T]CCCCATCTCCTAAGC | 106039 |
rs213055723 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879175 | CTTGCCAGGGGAGAT[A/G]AGCCCCCCCCCCCAC | 106039 |
rs213290596 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78888963 | CCTATCCGGAGGCCC[C/T]GCCACTTCTAACCCC | 106039 |
rs213337430 | snp | C/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879812 | GAGATGCTCTGTTTG[C/G]GCCAGTGAGTTTCAG | 106039 |
rs213362702 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880579 | ATCCAAGTCCCCTGC[A/G]CTGGGTTCCCATGCT | 106039 |
rs213501066 | snp | A/C | | | intron-variant | Gga1 | Mm_Celera | 15:78887627 | TGTGAGGCTGCCAAG[A/C]ACAAGCCTACCTCCT | 106039 |
rs213550328 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78890458 | ACAAGGCCATATATG[C/T]GGCTGGAGCCATGGG | 106039 |
rs213930360 | in-del | -/C | | | intron-variant | Gga1 | GRCm38.p3 | 15:78889683 | CCGCTGCTCCCAGTG[-/C]CCCCCAGGACCTGCC | 106039 |
rs214010513 | in-del | -/A | | | intron-variant | Gga1 | GRCm38.p3 | 15:78889309 | TCATTAGACTTCCAG[-/A]AAAAAAGGACAGAGC | 106039 |
rs214228673 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78881179 | TGTGCCCCTGCCATG[C/T]AGGCTGGAGACCCAG | 106039 |
rs214435066 | snp | C/T | | | intron-variant | Gga1 | Mm_Celera | 15:78885607 | GCTGTTGAAATAAGT[C/T]CCCGGCCAGCTCCCA | 106039 |
rs214527398 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78883213 | CCCTCCAGGGTCCTT[C/T]CCTCCCTCTGGGCCC | 106039 |
rs214553018 | snp | A/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78884019 | CATCTGAGAGGCTGC[A/T]GGGTTAGGGCTCAAG | 106039 |
rs214717362 | in-del | -/GCACTCACAAA | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880413 | GCAGAAGTGAAGAAG[-/GCACTCACAAA]GCACCCTTGGAAGAA | 106039 |
rs215007423 | in-del | -/CTCC | | | intron-variant | Gga1 | GRCm38.p3 | 15:78881020 | ACTCTCCCATACTGA[-/CTCC]CTCTGCTCCTGCAGA | 106039 |
rs215032995 | snp | A/G | | | intron-variant | Gga1 | Mm_Celera | 15:78887782 | TGGGTTGTGAGTGCT[A/G]ACCGAGGATGGGCAA | 106039 |
rs215090845 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78888640 | TGAGAAGGCCACAGA[A/G]AGCAGACTGCTCTTG | 106039 |
rs215187381 | snp | C/T | | | intron-variant | Gga1 | Mm_Celera | 15:78887146 | GCTACAGAATGAAAC[C/T]TTGTCAGAAACCAAA | 106039 |
rs215268006 | in-del | -/A | | | intron-variant | Gga1 | GRCm38.p3 | 15:78886786 | CTGCCTCTGCCTCCC[-/A]AAGTGCTGGGATTAA | 106039 |
rs215444743 | snp | C/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880088 | TTCTGCCTCACAGTG[C/G]ACAGCCTGCGTACTG | 106039 |
rs215535743 | snp | G/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879900 | AAGTGAATGGCTGCC[G/T]GACACTGAGGGTGTC | 106039 |
rs215597596 | snp | C/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78881325 | AACTGAGGCTCAACT[C/G]TCTGGTCTTGAACCT | 106039 |
rs215597757 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78890815 | TGTGTGCCACCCTGT[A/G]CCATAGCGGAGAGCT | 106039 |
rs215719805 | snp | A/G | | | synonymous-codon | Gga1 | GRCm38.p3 | 15:78889786 | CACCCAGCCAGCCAC[A/G]CCCACCCGCCCTGGC | 106039 |
rs215925970 | in-del | -/C | | | downstream-variant-500B, nc-transcript-variant | Gga1, LOC102632079 | GRCm38.p3 | 15:78894878 | TCCTGCACTCTGCAG[-/C]CCGGTCTTGTGTTTC | 106039 |
rs216012190 | snp | A/G | | | intron-variant, downstream-variant-500B | Gga1, Mir6955 | GRCm38.p3 | 15:78892346 | AGGATGCTGAGGCAA[A/G]GAGTGGGGGGGCTCC | 106039 |
rs216173647 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78884366 | GACAAAAGATGGTAA[C/T]GGATCAAGTTTACCT | 106039 |
rs216427901 | snp | A/G | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78875291 | GGTGGCACCATCCCC[A/G]ATGGGGAACCTGTAC | 106039 |
rs216435317 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880435 | TTGGAAGAAGTGTTC[C/T]TGAGCCACTCCCCAG | 106039 |
rs216462711 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | Gga1, LOC102632079 | GRCm38.p3 | 15:78894341 | GAGCTCTCCACTCAG[-/C]CCCCGGGGCCTCCAG | 106039 |
rs216740017 | snp | C/T | | | intron-variant | Gga1 | Mm_Celera | 15:78886946 | GGCAGGAGGAATTCC[C/T]GTGAGTTTAGGCTGG | 106039 |
rs216740131 | snp | A/G | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78877089 | CTCATCGCGTTGGCG[A/G]CGGCCACAGTGCCCA | 106039 |
rs216793690 | in-del | -/GCTCCATCCCCA | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78875650 | TATATGAAATGCTAG[-/GCTCCATCCCCA]GTACCACAGAAATCG | 106039 |
rs217221323 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880527 | TTACCTGAGCAGAGC[A/G]GCCCTCAGCCTGGGC | 106039 |
rs217249613 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78881006 | GAGGCAGGACTCCCA[C/T]TCTCCCATACTGACT | 106039 |
rs217360327 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78893496 | GAAGGGAGCTGCCTC[C/T]GCTGTGGTGGCTGCC | 106039 |
rs218751265 | snp | A/G | | | intron-variant | Gga1 | Mm_Celera | 15:78887878 | GTGATGTGACTGAGG[A/G]CCACCTCTAGAGACT | 106039 |
rs219086825 | snp | C/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78888753 | AGCTCAGGTCACAGC[C/G]CCAGTGTATCACATC | 106039 |
rs219418202 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78889407 | GAAAAGGCTAGCAGC[A/G]AGGGAGTCTTGGCAG | 106039 |
rs219458304 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78890971 | TGCCAGCCAGCAGGC[C/T]GTCCCCAGGGCCCTC | 106039 |
rs219494414 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879609 | TCTCAAGGACTGGAG[A/G]GTCACCCACAAGGTT | 106039 |
rs219776359 | in-del | -/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78881586 | CGCACAGTGAGCTCC[-/G]CCCCCACCCTCCTCT | 106039 |
rs220139065 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78892934 | TAGGTAGCAGTAGGT[A/G]ACATTGGCTGACTGA | 106039 |
rs220391569 | snp | A/G | | | intron-variant | Gga1 | Mm_Celera | 15:78888332 | CCCACCCCAGCTCAC[A/G]CCCAGCCCATCCAAC | 106039 |
rs220434684 | snp | A/C | | | intron-variant | Gga1 | Mm_Celera | 15:78885844 | TGGTGCTGCCCACAG[A/C]CATTTACTTGTCTCT | 106039 |
rs220436792 | snp | G/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78893690 | GTGCCCCAGGGTGGC[G/T]CTAACCTCCCTTCCC | 106039 |
rs220469831 | snp | A/G | | | intron-variant | Gga1 | Mm_Celera | 15:78886646 | TGTGCATACACAGAG[A/G]GCAAAACACAGATGT | 106039 |
rs220473150 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78883635 | TGAGCCTCAGTGTCC[A/G]AAGCCAGAAACCTTA | 106039 |
rs220483477 | in-del | -/T | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78876683 | ACCTTGTAGGATATA[-/T]TATCTGGCCTTGTCT | 106039 |
rs220587373 | snp | A/C | | | downstream-variant-500B, nc-transcript-variant | Gga1, LOC102632079 | GRCm38.p3 | 15:78894972 | TAAAAGGCTGGTCCC[A/C]AGCAGGGTGCAGAAA | 106039 |
rs220874963 | snp | C/T | | | intron-variant | Gga1 | Mm_Celera | 15:78886560 | TAGAATGCTTGCCAG[C/T]ATGCATGAGGTCCTG | 106039 |
rs220910325 | in-del | -/CATCCT | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879960 | ACTGAGCAGGTGCCA[-/CATCCT]GGGCCCTAGCCTCTT | 106039 |
rs220921116 | snp | A/G | | | utr-variant-5-prime | Gga1 | GRCm38.p3 | 15:78877514 | GAGGGCGGAGCCGAG[A/G]AGTTCCCGCGAGAGC | 106039 |
rs220982478 | snp | C/T | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78875948 | GGTTTTTGTTTTGGG[C/T]TTTGTTCTGTGTAGC | 106039 |
rs221274247 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880265 | TCCAGCCCCATCCTC[C/T]CTGCCACCAATCCCT | 106039 |
rs221465658 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78881568 | CTGGGTGATAGAACG[C/T]TCCGCACAGTGAGCT | 106039 |
rs221493433 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78882460 | GTCTTGGAACTCACT[C/T]TGTAGACCAGGCTGG | 106039 |
rs221583159 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78890090 | AGATGGGGTGATTCC[A/G]GGAGTGGAGTTGCCC | 106039 |
rs221634888 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880711 | CAGTCTCCTGAGTAT[A/G]GATACCAGGAGGATT | 106039 |
rs221653833 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880176 | TTCACCCGGCAGTGT[C/T]GGGGGCTCCACAAGG | 106039 |
rs221700500 | in-del | -/TTTT | | | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78890243 | CTGATCTCTTTGGCC[-/TTTT]TTTTTTTTTTTTTTT | 106039 |
rs221719202 | snp | A/G | | | missense | Gga1 | GRCm38.p3 | 15:78883290 | AGACGTGCATGAAGA[A/G]CTGCGGCAAGAGGTT | 106039 |
rs221726344 | in-del | -/GCAGCCT | | | intron-variant | Gga1 | GRCm38.p3 | 15:78893397 | CTTTAGACCTGGTGG[-/GCAGCCT]GCTGCCTGGGCATGG | 106039 |
rs221885175 | snp | C/T | | | intron-variant | Gga1 | Mm_Celera | 15:78888052 | AGCCCTCTTCCCAGA[C/T]TCGGGTGCCATTACC | 106039 |
rs222337581 | snp | C/T | | | intron-variant | Gga1 | Mm_Celera | 15:78887366 | ATCCAGAAATGTGAA[C/T]GTTTACATGAAATCT | 106039 |
rs222371363 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879366 | CCTTGCTGGGGCTCA[C/T]GTGCCTTTGACACTT | 106039 |
rs222489598 | snp | G/T | | | intron-variant | Gga1 | Mm_Celera | 15:78886680 | TATGTTTGTTTTTTT[G/T]TTTTTTTTTGAGACA | 106039 |
rs222513326 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78884806 | TGGAGCTGGTAATTA[A/G]AAATTACCAAAGCCC | 106039 |
rs222547369 | snp | C/T | | | intron-variant | Gga1 | Mm_Celera | 15:78885675 | GCTGGGGTGGGGGTG[C/T]ATGCTGAGGCCACCC | 106039 |
rs222652533 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78881535 | TTGGTCTGGATGTCC[C/T]CAGGCTCCTTGGTGC | 106039 |
rs222714746 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880127 | TACAAGTAGGGAAAC[A/G]GAGGTTCAAGAAGTT | 106039 |
rs222802737 | snp | G/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78882390 | TTCATAGGACACATG[G/T]TTTTTTTTGTTTTTT | 106039 |
rs222907804 | snp | C/G | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78875780 | TGCAGGTGTGGTGAT[C/G]CACGCAGAAGGTGGA | 106039 |
rs222940087 | in-del | -/TAAA | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78875906 | GTAGTGATCTGACTT[-/TAAA]TAAATCAATTTGGCA | 106039 |
rs223322341 | in-del | -/CCAA | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879188 | TGAGCCCCCCCCCCC[-/CCAA]ACACACACACACACA | 106039 |
rs223336696 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78883757 | CCTCTGAACAGAACT[C/T]AGAGTGGGCTGTGCA | 106039 |
rs223340197 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78881130 | TTTGAGGGGTAGGTG[A/G]CTCTCTTTGGCTGAC | 106039 |
rs223682000 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78884593 | CAAAAGGAATTACAC[A/G]CTACCCTTTCTCAAA | 106039 |
rs224001372 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879205 | CACACACACACACAC[A/G]CACACGCACTGTGGA | 106039 |
rs224228708 | in-del | -/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78886672 | GATGTTAATATGTTT[-/G]TTTTTTTGTTTTTTT | 106039 |
rs224231176 | snp | C/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78877830 | CCGCCCACCCACCCC[C/G]GTGACCCGGTGGCGC | 106039 |
rs224408700 | in-del | -/AAG | | | intron-variant | Gga1 | GRCm38.p3 | 15:78883051 | GAAACCCTGTCTCTA[-/AAG]AAGAATCGTAAAATG | 106039 |
rs224992380 | in-del | -/GCGT | | | intron-variant | Gga1 | Mm_Celera | 15:78887558 | GTGCAGCAGGAGAGG[-/GCGT]GCGTGTCACGGCCTG | 106039 |
rs225086229 | in-del | -/AGGCGGAAAA | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78876915 | ATGTCTGCACTTGGG[-/AGGCGGAAAA]AGGCGGATCTCAGGA | 106039 |
rs225643725 | in-del | -/AACACTTCTGCCTCACAGTGCAC | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880068 | TCCCAGAACCATGAG[-/AACACTTCTGCCTCACAGTGCAC]AGCCTGCGTACTGTC | 106039 |
rs225773829 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Gga1, LOC102632079 | GRCm38.p3 | 15:78893977 | CCCAGCAGGAGGCTG[C/T]GCCTGGGTCTGCCAT | 106039 |
rs225972863 | in-del | -/TATGCA | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78876765 | GAATGCAGAATTAAG[-/TATGCA]TACTCGGTGCAAGCA | 106039 |
rs225990550 | snp | C/T | | | downstream-variant-500B, nc-transcript-variant | Gga1, LOC102632079 | GRCm38.p3 | 15:78894857 | AAGGTCCCAGCTGCT[C/T]GCTTCCTCCTGCACT | 106039 |
rs226006417 | in-del | -/AACCCACTCAT | | | intron-variant | Gga1 | GRCm38.p3 | 15:78888365 | ACCCCAGCCCACCCC[-/AACCCACTCAT]AACCCACTCATAACC | 106039 |
rs226325301 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78893154 | GACCGACCTCCTACC[C/T]GTCCTCCCACAGGCA | 106039 |
rs226511829 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78890721 | GGCCCTGGCTGTCTT[A/G]GAACTTACCCTGTAG | 106039 |
rs226572403 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78891686 | AGCTTAGGGTCCTGA[C/T]AGGACCACAGTTCCA | 106039 |
rs226607290 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Gga1, LOC102632079 | GRCm38.p3 | 15:78894407 | GGAAACTTGAAAGCA[A/G]AGCCAGAGGACATGC | 106039 |
rs226627902 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78884258 | GCCCCACCTGCAGCT[C/T]GGGCCTTCTGCCAGC | 106039 |
rs226663193 | snp | C/T | | | intron-variant | Gga1 | Mm_Celera | 15:78885203 | CAGATCCGTCTCCTG[C/T]GACCTCTGGAGCTGA | 106039 |
rs226734794 | snp | C/G | | | intron-variant | Gga1 | Mm_Celera | 15:78887252 | CCGCAGGAAAAGAAA[C/G]GATCAAGGCCACATG | 106039 |
rs226985674 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78889910 | CCTGCTGGCACCAGC[A/G]TTCTGCTGGCACACA | 106039 |
rs227128151 | in-del | -/TTTTTG | | | intron-variant | Gga1 | GRCm38.p3 | 15:78882401 | CATGTTTTTTTTTGT[-/TTTTTG]TTTTTTTCAAGACAG | 106039 |
rs227263252 | in-del | -/TTTT | | | intron-variant | Gga1 | Mm_Celera | 15:78886668 | ACAGATGTTAATATG[-/TTTT]TTTGTTTTTTTGTTT | 106039 |
rs227419869 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78888643 | GAAGGCCACAGAAAG[C/T]AGACTGCTCTTGGAA | 106039 |
rs227714465 | snp | C/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78889500 | AGTAACACCTTAGGT[C/G]CTTGGTTGGTATCGC | 106039 |
rs227731756 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880447 | TTCCTGAGCCACTCC[C/T]CAGGGACAAGGTCTG | 106039 |
rs227733233 | snp | A/G | | | intron-variant | Gga1 | Mm_Celera | 15:78886908 | GGCTGGCTCACCTTC[A/G]ATCCCAGCACTTGGG | 106039 |
rs227764678 | snp | A/G | | | intron-variant | Gga1 | Mm_Celera | 15:78887431 | CCACGTTTTAATAGT[A/G]TGTGCCCCACCGAGA | 106039 |
rs227882417 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78881712 | GGAAAGGAAGGAGCC[C/T]GGGTGCTCATGAGCC | 106039 |
rs228150784 | snp | A/C | | | intron-variant | Gga1 | GRCm38.p3 | 15:78889605 | CGGGCTGGAGTGGCT[A/C]TGAGGGGCTAGGAGA | 106039 |
rs228423555 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78890848 | CAGCTGCTGCCTGCC[C/T]GCTGAAGAGCACTTG | 106039 |
rs228433353 | in-del | -/TG | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78875951 | TTTTGTTTTGGGTTT[-/TG]TTCTGTGTAGCCCTG | 106039 |
rs228465598 | snp | G/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78893116 | AAGAGGCCAGCGCCT[G/T]GTATGATCTGACTCC | 106039 |
rs228528731 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78882995 | TCTCTGTGACTTTGA[A/G]GTCTACAGAGTGAGT | 106039 |
rs228549512 | snp | C/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78883853 | GAGCTGATGTGTGGG[C/G]CCTCATGGCTGCACA | 106039 |
rs228707934 | snp | C/T | | | intron-variant | Gga1 | Mm_Celera | 15:78885456 | CATCCTGTGTGGAGC[C/T]GGCTGAATGCACTGA | 106039 |
rs228824955 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78878841 | AACTCAAGCAGGTCA[A/G]GAAGCAGGAGCTGAT | 106039 |
rs228909319 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78878019 | AGGGGGGACCCCTGG[C/T]CCATCTGATCCAGCT | 106039 |
rs228963591 | snp | C/T | | | missense, downstream-variant-500B | Gga1, Mir6955 | GRCm38.p3 | 15:78891957 | CTCCTCCAGCCCAGG[C/T]CCCCAGCATGGACTG | 106039 |
rs229021022 | snp | C/G | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78875359 | CCACACTCTCTCTGC[C/G]CTGTTTCTCAGCTGC | 106039 |
rs229022939 | snp | A/G | | | intron-variant | Gga1 | Mm_Celera | 15:78886017 | ACACAGGAGCTGTGC[A/G]TGTGTGTACATATGA | 106039 |
rs229081170 | snp | A/G | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78876733 | CCGAATAACCCAAAT[A/G]CAAGGAGTTTCTAAA | 106039 |
rs229555453 | snp | A/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879775 | TTCATAGCGCTTCTG[A/T]GATCGCTAATCTGAG | 106039 |
rs229589118 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880308 | AGAGCGGAGCAAGGC[A/G]TGTTCTCTGCAGGAG | 106039 |
rs229673308 | in-del | -/TG | | | intron-variant | Gga1 | GRCm38.p3 | 15:78884070 | CGAGAAGTCCCCTTC[-/TG]TGTGTCTCTGAAGTA | 106039 |
rs229896320 | in-del | -/G | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78876791 | AGCACTGACCCCTAA[-/G]TGACCTCAGGCAAAC | 106039 |
rs229951964 | snp | C/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880150 | AAGAAGTTCTTCTTA[C/G]TGCACGGCTCTTCAC | 106039 |
rs230121689 | in-del | -/CCCAGCTCACT | | | intron-variant | Gga1 | Mm_Celera | 15:78888269 | CCTGCTCCCACCCAC[-/CCCAGCTCACT]CCCAGCTCACTCCCA | 106039 |
rs230239257 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880386 | GCTAGGAACATAGCC[A/G]CTGCCGTGGTGGGCA | 106039 |
rs230440106 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78888541 | AGGCCCAGCCCTGTC[C/T]TACCTCCTCCCACTT | 106039 |
rs230467288 | snp | G/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880885 | CCCACTGATCCCACC[G/T]GAAGGTCAGTGCTCA | 106039 |
rs230771579 | snp | C/T | | | downstream-variant-500B, nc-transcript-variant | Gga1, LOC102632079 | GRCm38.p3 | 15:78894688 | CCAGCTCCCACCCAT[C/T]CCAGCCCCTCAGCCC | 106039 |
rs230855739 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78893688 | CAGTGCCCCAGGGTG[A/G]CGCTAACCTCCCTTC | 106039 |
rs231063378 | in-del | -/CA | | | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78891745 | AACTTAAGGTCCCCC[-/CA]GTGTGGAGATCCATT | 106039 |
rs231189572 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78881759 | GCACTCGAGCTGTTA[C/T]CACCTGATCTTACCA | 106039 |
rs231331446 | snp | A/C | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78875254 | CCTGAGTCTACTGAG[A/C]TGGGAAGACCTGCCC | 106039 |
rs231406084 | in-del | -/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78893484 | CTGAGACTCTGGGAA[-/G]GGAGCTGCCTCTGCT | 106039 |
rs231754892 | snp | A/T | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78876101 | TTCATTAACAATTTT[A/T]AAAATAAAGAAAACA | 106039 |
rs232026759 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78878585 | AGGAGAGTCAGCCTG[A/G]CAGTGGGGTTGATTG | 106039 |
rs232321542 | in-del | -/ACCT | | | intron-variant | Gga1 | GRCm38.p3 | 15:78886608 | CCCCAAACATATGTA[-/ACCT]AGTATGGGTGTGTAT | 106039 |
rs232338355 | in-del | -/A | | | intron-variant | Gga1 | Mm_Celera | 15:78885025 | CTAAAAATAAGTCTT[-/A]AAAAAAAACAAAAGG | 106039 |
rs232355225 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78889665 | GGAGGAGTGCTGTGC[C/T]CACCGCTGCTCCCAG | 106039 |
rs232459849 | snp | A/C | | | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78891235 | TGGGGCCTTGCTGGA[A/C]GGAGAGGAAGTTAAT | 106039 |
rs232471983 | snp | C/G | | | intron-variant, downstream-variant-500B | Gga1, Mir6955 | GRCm38.p3 | 15:78892212 | CCCACTGTGACAAGG[C/G]TGTGCCCAGGGATGG | 106039 |
rs232512410 | snp | C/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880090 | CTGCCTCACAGTGCA[C/G]AGCCTGCGTACTGTC | 106039 |
rs232516300 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78888976 | CCCGCCACTTCTAAC[C/T]CCCCTCTCCTCGCCT | 106039 |
rs232791563 | snp | A/C | | | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78891713 | TCCACCTTCAAGGTT[A/C]AGCTCTTCTTCCCTT | 106039 |
rs233257933 | in-del | -/GAACTCG | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78876004 | GACCAGGCTGACTTT[-/GAACTCG]GAGATTCACCTGCCT | 106039 |
rs233425684 | in-del | -/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78884226 | AGTGAGCCCCAGCGT[-/G]GGGGGACCCGTGACA | 106039 |
rs233429273 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880057 | GGGCAGAAGTGTCCC[A/G]GAACCATGAGAACAC | 106039 |
rs233535449 | snp | A/C | | | intron-variant | Gga1 | Mm_Celera | 15:78887165 | TCAGAAACCAAACCC[A/C]GATCTCTGGTTAGCA | 106039 |
rs233557559 | snp | A/G | | | intron-variant | Gga1 | Mm_Celera | 15:78887836 | GGAGGGGAGAAATGC[A/G]AGCCATGGTCACGAG | 106039 |
rs233569722 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879211 | CACACACACGCACAC[A/G]CACTGTGGAGGTTGG | 106039 |
rs233657978 | in-del | -/C | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879587 | CCTCACTGGTGACAT[-/C]TGTTCCTCTCAAGGA | 106039 |
rs233802826 | snp | A/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78893693 | CCCCAGGGTGGCGCT[A/T]ACCTCCCTTCCCCAC | 106039 |
rs233960496 | snp | C/G | | | intron-variant | Gga1 | Mm_Celera | 15:78886212 | TCTGTAATCTTGGAA[C/G]TCCAGAGGCTGAAGC | 106039 |
rs234175223 | snp | A/G | | | intron-variant | Gga1 | Mm_Celera | 15:78885611 | TTGAAATAAGTCCCC[A/G]GCCAGCTCCCAAGGC | 106039 |
rs234209117 | in-del | -/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78884748 | AGGGGAGTGGCTGCG[-/T]TTTTACCTCCACAGG | 106039 |
rs234371906 | snp | C/G | | | downstream-variant-500B, nc-transcript-variant | Gga1, LOC102632079 | GRCm38.p3 | 15:78895041 | GGAGCTGCCTTAGAG[C/G]CCCATACTGCAGGAA | 106039 |
rs234725151 | snp | C/T | | | synonymous-codon | Gga1 | GRCm38.p3 | 15:78883294 | GTGCATGAAGAGCTG[C/T]GGCAAGAGGTTCCAT | 106039 |
rs234766663 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78884442 | CTCAACTGGTAGAAT[A/G]CTTGCCTAGCATGCA | 106039 |
rs235034379 | snp | A/T | | | intron-variant | Gga1 | Mm_Celera | 15:78887614 | AAGGGCTAAGCGATG[A/T]GAGGCTGCCAAGCAC | 106039 |
rs235226210 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78882073 | CAGGCTAATGGAGTG[A/G]CTGTCCCTCTGAGTG | 106039 |
rs235343013 | snp | A/G | | | missense | Gga1 | GRCm38.p3 | 15:78889809 | GCCCTGGCAACCAGA[A/G]CAGTCCTGAGCAGCT | 106039 |
rs235360723 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78881345 | GTCTTGAACCTTACC[A/G]GGACATGAGGAGTCC | 106039 |
rs235541392 | snp | G/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78884567 | AGGGCCACCCTGAGC[G/T]ACATAGGATTCAAAA | 106039 |
rs235688224 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78878063 | GAGAAACTCCCAGTG[C/T]TTGAAAGGGTCCCGT | 106039 |
rs235911507 | snp | A/T | | | intron-variant | Gga1 | Mm_Celera | 15:78887884 | TGACTGAGGACCACC[A/T]CTAGAGACTTGAGCC | 106039 |
rs236212982 | snp | G/T | | | intron-variant | Gga1 | Mm_Celera | 15:78886579 | CATGAGGTCCTGGTG[G/T]CTGTCCTCTGTATCC | 106039 |
rs236300339 | snp | A/G | | | intron-variant | Gga1 | Mm_Celera | 15:78885705 | CTTCTGCTATGCTCC[A/G]TGGGGAGTGTGTGCA | 106039 |
rs236405365 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879833 | TGAGTTTCAGGAAAG[A/G]AGAGCTTTTGTCCAC | 106039 |
rs236585367 | snp | C/T | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78877134 | GGACTTTGACATCTT[C/T]CCACGTAAGCGGAAG | 106039 |
rs236747489 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78889920 | CCAGCGTTCTGCTGG[C/T]ACACAGCAATGGCCC | 106039 |
rs236971040 | snp | G/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78881260 | TGGGGGCTTCAGGGG[G/T]GCCGCCCCCTTGAGG | 106039 |
rs236996275 | snp | A/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78883109 | AAGCCACGGAGGCCC[A/T]GTGGTCGAGCAACCT | 106039 |
rs237170597 | in-del | -/GG | | | intron-variant, downstream-variant-500B | Gga1, Mir6955 | GRCm38.p3 | 15:78892350 | GCTGAGGCAAGGAGT[-/GG]GGGGGGGCTCCCCCT | 106039 |
rs237211011 | snp | A/G | | | downstream-variant-500B, nc-transcript-variant | Gga1, LOC102632079 | GRCm38.p3 | 15:78894953 | TACTCTTCACCCGGC[A/G]TGGTAAAAGGCTGGT | 106039 |
rs237231610 | snp | A/C | | | intron-variant | Gga1 | GRCm38.p3 | 15:78883259 | CTACCTCAGTGCTTC[A/C]CCCCACAGGTTCTGG | 106039 |
rs237298871 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Gga1, LOC102632079 | GRCm38.p3 | 15:78894245 | GTGGGGGTGACGCCC[A/G]CGCCCTAGCTGTGTG | 106039 |
rs237523288 | snp | A/G | | | intron-variant | Gga1 | Mm_Celera | 15:78885551 | TAGCTTTATCTTTCT[A/G]TACTAGTGGAGCAGT | 106039 |
rs237624905 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880360 | TCCACTTGGGCCCTC[C/T]GTAAAGAATAGCTAG | 106039 |
rs237852345 | snp | A/C | | | intron-variant | Gga1 | Mm_Celera | 15:78887076 | ACCTCTAATCCCAAC[A/C]CTGGGGAGGCTAAGA | 106039 |
rs238472910 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78890027 | AGAGACTGAGAACAA[A/G]ATCAGCGTGGCAGAA | 106039 |
rs238574082 | snp | C/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78889426 | GAGTCTTGGCAGGTC[C/G]GGAGGAGCCAAGCCT | 106039 |
rs238649497 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880709 | CTCAGTCTCCTGAGT[A/G]TGGATACCAGGAGGA | 106039 |
rs238885254 | in-del | -/CC | | | intron-variant | Gga1 | GRCm38.p3 | 15:78888712 | AGGAGGGAGAACTCT[-/CC]CCCCATCTCCTAAGC | 106039 |
rs239089135 | in-del | -/CGCACACG | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879204 | ACACACACACACACA[-/CGCACACG]CACTGTGGAGGTTGG | 106039 |
rs239469007 | snp | G/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78882422 | TTTTTTTCAAGACAG[G/T]GTTTCTCTGTGTAGT | 106039 |
rs239473600 | snp | A/G | | | intron-variant | Gga1 | Mm_Celera | 15:78888055 | CCTCTTCCCAGACTC[A/G]GGTGCCATTACCTCC | 106039 |
rs239499671 | in-del | -/GTCTGCCTTTACT | | | intron-variant | Gga1 | GRCm38.p3 | 15:78884277 | CCTTCTGCCAGCAAG[-/GTCTGCCTTTACT]GTCTCAAGAACACAG | 106039 |
rs239600492 | snp | A/C | | | intron-variant, downstream-variant-500B | Gga1, Mir6955 | GRCm38.p3 | 15:78892363 | AGTGGGGGGGCTCCC[A/C]CTGCGGATGGGGGTT | 106039 |
rs239727681 | in-del | -/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880501 | GTCCAGTCTTTCCCA[-/G]GGCTATGTCCTTACC | 106039 |
rs239741793 | snp | A/G | | | intron-variant | Gga1 | Mm_Celera | 15:78886656 | CAGAGAGCAAAACAC[A/G]GATGTTAATATGTTT | 106039 |
rs239754647 | snp | A/G | | | downstream-variant-500B, nc-transcript-variant | Gga1, LOC102632079 | GRCm38.p3 | 15:78895000 | AAACCACCCAGCGAG[A/G]ACAACCTGCCAGTGG | 106039 |
rs240446955 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78883758 | CTCTGAACAGAACTC[A/G]GAGTGGGCTGTGCAG | 106039 |
rs240459204 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78891702 | AGGACCACAGTTCCA[C/T]CTTCAAGGTTCAGCT | 106039 |
rs240513432 | snp | C/T | | | intron-variant | Gga1 | Mm_Celera | 15:78886971 | GGCTGGCCTGGTCTA[C/T]AGCGAGTTCCGAGAC | 106039 |
rs240518896 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78892935 | AGGTAGCAGTAGGTA[A/G]CATTGGCTGACTGAC | 106039 |
rs240675609 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78884617 | TCTCAAAAACTATGT[A/G]TGGGGTTTGGAGAGA | 106039 |
rs240909475 | snp | A/T | | | intron-variant | Gga1 | Mm_Celera | 15:78887274 | GGCCACATGGCAGGT[A/T]CCTCTGAGGCAGGAG | 106039 |
rs240946864 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78882533 | GGAATTAAAGGCATG[C/T]GCCACCACTGCCCGA | 106039 |
rs241002496 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78881571 | GGTGATAGAACGCTC[C/T]GCACAGTGAGCTCCG | 106039 |
rs241274270 | in-del | -/TTTT | | | intron-variant | Gga1 | GRCm38.p3 | 15:78884796 | CAAGCCCCATGGAGC[-/TTTT]TGGTAATTAAAAATT | 106039 |
rs241554873 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880301 | ATCCATGAGAGCGGA[A/G]CAAGGCATGTTCTCT | 106039 |
rs241566664 | snp | C/T | | | intron-variant | Gga1 | Mm_Celera | 15:78887510 | GGGGCTCAGCCTGGG[C/T]CCAGCTTGACTGTCA | 106039 |
rs241617062 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78889341 | TTAGATGCAAACTTG[A/G]CTCTTCTCAGGGGAC | 106039 |
rs241625071 | snp | C/G | | | synonymous-codon | Gga1 | Mm_Celera | 15:78888197 | GCTGACAGAGATGGT[C/G]ATGAGCCACAGCCAG | 106039 |
rs241660058 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880826 | TCTCTGAGGATGGGG[C/T]CTTTGGGAGAAGGCG | 106039 |
rs241686166 | in-del | -/TCCCACCCATCAT | | | intron-variant | Gga1 | Mm_Celera | 15:78885117 | GCAGGGCAGAAGTAG[-/TCCCACCCATCAT]TCCCAAGCCAGGGAG | 106039 |
rs241777327 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880749 | TGCTCTTGAGAACAG[C/T]GTGAGAGATGGGAAA | 106039 |
rs241911020 | in-del | -/CCAACCCACCCCAGCCCACC | | | intron-variant | Gga1 | GRCm38.p3 | 15:78888343 | TCACACCCAGCCCAT[-/CCAACCCACCCCAGCCCACC]CCAACCCACTCATAA | 106039 |
rs242374299 | snp | G/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78882563 | ACCGTAGGACACATG[G/T]TAAACACACTGAATC | 106039 |
rs242533515 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78893519 | TGGCTGCCTGACCAG[C/T]AGTCACCTCCTGCCC | 106039 |
rs242701310 | snp | A/C | | | intron-variant | Gga1 | GRCm38.p3 | 15:78883854 | AGCTGATGTGTGGGG[A/C]CTCATGGCTGCACAC | 106039 |
rs242737134 | snp | A/G | | | intron-variant | Gga1 | Mm_Celera | 15:78884991 | GCTGGGATTAAAGGC[A/G]TGCGCCACCACCGCC | 106039 |
rs242739120 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B | Gga1, LOC102632079 | GRCm38.p3 | 15:78893991 | GCGCCTGGGTCTGCC[A/T]TAGCTGCTGGGACCT | 106039 |
rs242797429 | snp | A/G | | | intron-variant | Gga1 | Mm_Celera | 15:78885141 | TCATTCCCAAGCCAG[A/G]GAGCTGATGAAAGTG | 106039 |
rs242915727 | snp | A/G | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78875787 | GTGGTGATGCACGCA[A/G]AAGGTGGAGAAAGAA | 106039 |
rs243568900 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78893119 | AGGCCAGCGCCTGGT[A/G]TGATCTGACTCCACC | 106039 |
rs243640064 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879805 | GTACTCAGAGATGCT[C/T]TGTTTGCGCCAGTGA | 106039 |
rs243700679 | snp | G/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78878964 | TGGTCCCACCCACAA[G/T]GGGCCTTTCCCCCTT | 106039 |
rs243881931 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880202 | CAAGGGGACTGTCTC[A/G]TATTATTTGCTCCTC | 106039 |
rs243975864 | in-del | -/CACCCATCATT | | | intron-variant | Gga1 | Mm_Celera | 15:78885120 | GGGCAGAAGTAGTCC[-/CACCCATCATT]CCCAAGCCAGGGAGC | 106039 |
rs244146757 | snp | C/T | | | intron-variant | Gga1 | Mm_Celera | 15:78888342 | CTCACACCCAGCCCA[C/T]CCAACCCACCCCAGC | 106039 |
rs244412245 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78881363 | ACATGAGGAGTCCTA[C/T]ACCTGGTCAAATCTA | 106039 |
rs244494237 | snp | C/G | | | intron-variant | Gga1 | Mm_Celera | 15:78887775 | TTGTTTCTGGGTTGT[C/G]AGTGCTGACCGAGGA | 106039 |
rs244585120 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78881566 | TCCTGGGTGATAGAA[C/T]GCTCCGCACAGTGAG | 106039 |
rs244673352 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78888635 | TCATCTGAGAAGGCC[A/G]CAGAAAGCAGACTGC | 106039 |
rs245048048 | snp | C/T | | | downstream-variant-500B, nc-transcript-variant | Gga1, LOC102632079 | GRCm38.p3 | 15:78894696 | CACCCATCCCAGCCC[C/T]TCAGCCCTGGGCCAG | 106039 |
rs245130663 | in-del | -/A | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879189 | TGAGCCCCCCCCCCC[-/A]CACACACACACACAC | 106039 |
rs245544442 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78884300 | TTACTGTCTCAAGAA[C/T]ACAGGGCCAGTGAGG | 106039 |
rs245747816 | snp | G/T | | | intron-variant | Gga1 | Mm_Celera | 15:78885375 | AGGCTGAGGAGCTGC[G/T]CTCCGGGAGAGCTCT | 106039 |
rs245916125 | snp | C/T | | | intron-variant | Gga1 | Mm_Celera | 15:78885791 | CACAGAGAGGTCCCA[C/T]ACACAGTAACCGAGG | 106039 |
rs245959829 | snp | A/T | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78876075 | CTGCCCGGCCTGCAG[A/T]TGGGTTTTATTTCAT | 106039 |
rs246011005 | snp | A/G | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78876380 | CCCGACGGCCGCCAG[A/G]GGCTACAGAGAGCGA | 106039 |
rs246119515 | in-del | -/A | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78876851 | GATTCATAGGTTAAG[-/A]AAAAAAAAAGACTTA | 106039 |
rs246196470 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78890751 | GACCAAGCTAGCCTT[A/G]AACTCAGAGATCCAC | 106039 |
rs246408463 | in-del | -/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78888372 | CCCACCCCAACCCAC[-/T]CATAACCCACTCATA | 106039 |
rs246449806 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78882861 | TTGGGGTTTCTTCCT[C/T]AAGTATGCAGGGATC | 106039 |
rs246589380 | snp | A/C | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879442 | GCCAGTACCCCGAAC[A/C]TTCTCCTTGCCTCCA | 106039 |
rs246609905 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880517 | GGCTATGTCCTTACC[C/T]GAGCAGAGCGGCCCT | 106039 |
rs246826765 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880998 | CGTTAGAGGAGGCAG[A/G]ACTCCCACTCTCCCA | 106039 |
rs247586867 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78890224 | TGAAAGTGAAGAAGT[A/G]AACTCTGATCTCTTT | 106039 |
rs247669247 | in-del | -/TTC | | | intron-variant | Gga1 | Mm_Celera | 15:78887935 | GGACTCTGGCAGAAG[-/TTC]GGTAGGGAGTGGCAT | 106039 |
rs247748089 | snp | C/T | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78875361 | ACACTCTCTCTGCCC[C/T]GTTTCTCAGCTGCAG | 106039 |
rs248087051 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78893046 | ACCCACACTTTGAAC[A/G]GAGCCTGGGAAGGGC | 106039 |
rs248270844 | in-del | -/C | | | utr-variant-3-prime, downstream-variant-500B | Gga1, LOC102632079 | GRCm38.p3 | 15:78893879 | GGAGGGGCAGCAGGA[-/C]CTGGACCTGTTCATC | 106039 |
rs248459267 | snp | A/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78882075 | GGCTAATGGAGTGGC[A/T]GTCCCTCTGAGTGAA | 106039 |
rs248499569 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78883088 | TGTGCAAGTGATACT[C/T]GGGCCAAGCCACGGA | 106039 |
rs248625515 | snp | C/T | | | downstream-variant-500B, nc-transcript-variant | Gga1, LOC102632079 | GRCm38.p3 | 15:78895046 | TGCCTTAGAGCCCCA[C/T]ACTGCAGGAAGACAG | 106039 |
rs248881206 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78877940 | CCACTTCCTCAGGGC[C/T]TGAGTCTTTCAAACC | 106039 |
rs249179083 | in-del | -/TG | | | intron-variant | Gga1 | GRCm38.p3 | 15:78882361 | ATTCCTTAACTCACA[-/TG]CACAATGGACACCTT | 106039 |
rs249520764 | snp | C/G | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78876052 | GTGCTAGGTGGCGTG[C/G]GCCACCACTGCCCGG | 106039 |
rs249758163 | snp | C/T | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78877135 | GACTTTGACATCTTC[C/T]CACGTAAGCGGAAGT | 106039 |
rs249883014 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78881137 | GGTAGGTGGCTCTCT[C/T]TGGCTGACACACTCA | 106039 |
rs250170676 | snp | A/G | | | downstream-variant-500B, nc-transcript-variant | Gga1, LOC102632079 | GRCm38.p3 | 15:78894963 | CCGGCGTGGTAAAAG[A/G]CTGGTCCCAAGCAGG | 106039 |
rs250359720 | snp | C/T | | | intron-variant | Gga1 | Mm_Celera | 15:78887077 | CCTCTAATCCCAACA[C/T]TGGGGAGGCTAAGAC | 106039 |
rs250450495 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78883146 | TACTGGTCACTAGAC[A/G]ACCTCTGACCCAGTG | 106039 |
rs250999512 | in-del | -/C | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880910 | GCTCAGGCGTGGGGG[-/C]TGTCCAGCAAGAAGT | 106039 |
rs251115372 | snp | G/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78892888 | TCAAAGAAGGATCCA[G/T]GAGGAAGCCCCAGGT | 106039 |
rs251309042 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78891246 | TGGACGGAGAGGAAG[C/T]TAATGTGGGCTGCAA | 106039 |
rs251473520 | snp | C/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78883263 | CTCAGTGCTTCCCCC[C/G]ACAGGTTCTGGAGAC | 106039 |
rs251523842 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78882443 | TCTGTGTAGTCCTGC[C/T]TGTCTTGGAACTCAC | 106039 |
rs251543809 | snp | C/T | | | intron-variant, downstream-variant-500B | Gga1, Mir6955 | GRCm38.p3 | 15:78892264 | GAGAATGGGCCACAT[C/T]CACTGACCTGCATGC | 106039 |
rs251691334 | snp | G/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880389 | AGGAACATAGCCGCT[G/T]CCGTGGTGGGCAGAA | 106039 |
rs252202941 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880069 | CCCAGAACCATGAGA[A/G]CACTTCTGCCTCACA | 106039 |
rs252216083 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78881872 | CAAGTGGATCTACCA[A/G]TAAGCAACTTCTGCA | 106039 |
rs252323998 | snp | C/T | | | intron-variant | Gga1 | Mm_Celera | 15:78888083 | TCCCGAGGTCTGAGA[C/T]GGCCTTTGGCCATCT | 106039 |
rs252532739 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880068 | TCCCAGAACCATGAG[A/G]ACACTTCTGCCTCAC | 106039 |
rs252569273 | snp | C/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78888978 | CGCCACTTCTAACCC[C/G]CCTCTCCTCGCCTTC | 106039 |
rs252580424 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879240 | GGGGAAAGGGGTGGG[A/G]TCATGTCTCTTCCAG | 106039 |
rs252597358 | snp | A/G | | | intron-variant | Gga1 | Mm_Celera | 15:78887877 | GGTGATGTGACTGAG[A/G]ACCACCTCTAGAGAC | 106039 |
rs252597990 | in-del | -/TTGTGG | | | intron-variant | Gga1 | GRCm38.p3 | 15:78881513 | CCACAAGTGACTCCC[-/TTGTGG]CAGGGCTTGGTCTGG | 106039 |
rs252825129 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879537 | ATGTGCAGCCTGACC[C/T]AAGGAAGAAGAGATG | 106039 |
rs252903398 | snp | A/T | | | intron-variant | Gga1 | Mm_Celera | 15:78887023 | GTCTCAAGACAGAAA[A/T]ATTTCAAAAGGTGTT | 106039 |
rs253228823 | in-del | -/ACACACACACACAC | | | intron-variant | Gga1 | GRCm38.p3 | 15:78886450 | CACCATGGCACATGT[-/ACACACACACACAC]ACACACACACACACA | 106039 |
rs253286697 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78883576 | CCGGGCTGCTTAGGT[A/G]TTTGACATTTCTCCC | 106039 |
rs253492163 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Gga1, LOC102632079 | GRCm38.p3 | 15:78893909 | CCTGTGCTTCTCTCC[C/T]TCCTGTGGCCCCCAG | 106039 |
rs253506768 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78884693 | GTTTGATTTCCTACA[C/T]TCAGGTGAGGAAGCT | 106039 |
rs253638628 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78888961 | GCCCTATCCGGAGGC[C/T]CCGCCACTTCTAACC | 106039 |
rs253726649 | snp | A/G | | | intron-variant | Gga1 | Mm_Celera | 15:78885624 | CCGGCCAGCTCCCAA[A/G]GCTACCGCTGTGGTT | 106039 |
rs254090188 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78881733 | CTCATGAGCCACCTC[A/G]CATGGCCTTAGCACT | 106039 |
rs254188874 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78890475 | GCTGGAGCCATGGGT[C/T]CCTCCATGTGTACTC | 106039 |
rs254393438 | snp | G/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78878170 | CCTAGCCCCTGCTGA[G/T]CCTCCTCCCCAGGCC | 106039 |
rs254464990 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78890955 | GTCGTGCTGACTCTC[C/T]TGCCAGCCAGCAGGC | 106039 |
rs254813857 | snp | C/T | | | synonymous-codon | Gga1 | GRCm38.p3 | 15:78893568 | GCTGCAGCCACCTTC[C/T]GGCACAGAGCTGCCA | 106039 |
rs254971779 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78883998 | GGCCTATGAGGACTC[C/T]GGAGGCATCTGAGAG | 106039 |
rs254982419 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78881351 | AACCTTACCGGGACA[C/T]GAGGAGTCCTACACC | 106039 |
rs254998436 | snp | A/T | | | intron-variant | Gga1 | Mm_Celera | 15:78886022 | GGAGCTGTGCGTGTG[A/T]GTACATATGATGTCC | 106039 |
rs255415391 | snp | A/C | | | intron-variant | Gga1 | Mm_Celera | 15:78886552 | ACTTAGTGTAGAATG[A/C]TTGCCAGCATGCATG | 106039 |
rs255649827 | in-del | -/AA | | | intron-variant | Gga1 | Mm_Celera | 15:78885024 | CTAAAAATAAGTCTT[-/AA]AAAAAAAAACAAAAG | 106039 |
rs255697158 | snp | A/C | | | intron-variant | Gga1 | Mm_Celera | 15:78886079 | ACAGTAAAGAATTGA[A/C]AGGTGCTCAGAGGCT | 106039 |
rs255725766 | snp | A/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78893144 | TCCACCCACTGACCG[A/T]CCTCCTACCCGTCCT | 106039 |
rs255744286 | snp | C/T | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78876770 | GCAGAATTAAGTACT[C/T]GGTGCAAGCACTGAC | 106039 |
rs255864312 | in-del | -/TCCCTCCCCTGC | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879726 | CCCCAGCTCCTTCCA[-/TCCCTCCCCTGC]TCCCTCCCCTGCTCT | 106039 |
rs255932935 | snp | C/T | | | intron-variant | Gga1 | Mm_Celera | 15:78887952 | CGGTAGGGAGTGGCA[C/T]AATAGTGAGACACTG | 106039 |
rs255982197 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880155 | GTTCTTCTTACTGCA[C/T]GGCTCTTCACCCGGC | 106039 |
rs256461584 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879899 | TAAGTGAATGGCTGC[C/T]GGACACTGAGGGTGT | 106039 |
rs256559595 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78881381 | CTGGTCAAATCTAAC[C/T]GTGCCATGTGGCTGA | 106039 |
rs256634997 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78889959 | TTTGGGAAGCCAGTG[A/G]AGGCCATGGCGAGCA | 106039 |
rs256703659 | in-del | -/ATGTTTG | | | intron-variant | Gga1 | GRCm38.p3 | 15:78886666 | AACACAGATGTTAAT[-/ATGTTTG]TTTTTTTGTTTTTTT | 106039 |
rs256875436 | in-del | -/TCCTC | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78876028 | GATTCACCTGCCTCT[-/TCCTC]TCAAGTGCTAGGTGG | 106039 |
rs257184371 | snp | A/G | | | intron-variant | Gga1 | Mm_Celera | 15:78885601 | AGAGGAGCTGTTGAA[A/G]TAAGTCCCCGGCCAG | 106039 |
rs257209265 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78883736 | TGCCCAGCCCCCTGT[A/G]ACCTTCCTCTGAACA | 106039 |
rs257289603 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880951 | ATGTCCCATGTGCTC[A/G]ACCCCTCTTAACTGC | 106039 |
rs257316484 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78890070 | CAGCTCAGCCTGCCT[A/G]GGAGAGATGGGGTGA | 106039 |
rs257417239 | snp | A/G | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78875665 | GGTACCACAGAAATC[A/G]CCAGCTTGGGCTATA | 106039 |
rs257418511 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78891673 | GTGCCTGGGCGTCAG[C/T]TTAGGGTCCTGATAG | 106039 |
rs257549282 | snp | A/T | | | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78890540 | GGTACTGGTTGGTTC[A/T]TATTGTTGATCCTCC | 106039 |
rs257770111 | snp | A/C | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879189 | TGAGCCCCCCCCCCC[A/C]CACACACACACACAC | 106039 |
rs257971141 | snp | C/T | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78875272 | GGAAGACCTGCCCAC[C/T]GTGGGTGGCACCATC | 106039 |
rs258318220 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880710 | TCAGTCTCCTGAGTA[C/T]GGATACCAGGAGGAT | 106039 |
rs258582247 | in-del | -/TGCTTT | | | intron-variant | Gga1 | GRCm38.p3 | 15:78881801 | GGCCAGGGACACAGC[-/TGCTTT]TGCTTTTGCTGGTGA | 106039 |
rs258609226 | snp | A/G | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78876461 | GGGTGAAAGTACCTC[A/G]CATTTTGCCTCCTCC | 106039 |
rs258625339 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78877983 | CTCTTCTTAGATCTG[C/T]TCGGTCCCCCAGCCC | 106039 |
rs258677230 | snp | A/G | | | intron-variant | Gga1 | Mm_Celera | 15:78886004 | GAGCTAGGCCACCAC[A/G]CAGGAGCTGTGCGTG | 106039 |
rs258731409 | snp | A/G | | | intron-variant | Gga1 | Mm_Celera | 15:78886845 | TAATATGTTTAATGT[A/G]TAAGCTAGCATATGT | 106039 |
rs258926414 | snp | A/C | | | intron-variant | Gga1 | GRCm38.p3 | 15:78877774 | GTCTGTCGCTCCGCT[A/C]GGACCCTGGCAGCTG | 106039 |
rs259146006 | in-del | -/A | | | intron-variant | Gga1 | Mm_Celera | 15:78886264 | TAGTCTGGCCCACAT[-/A]AGCAAGACCCTGTCA | 106039 |
rs259352844 | snp | A/G | | | downstream-variant-500B, nc-transcript-variant | Gga1, LOC102632079 | GRCm38.p3 | 15:78894850 | CAAGGGGAAGGTCCC[A/G]GCTGCTCGCTTCCTC | 106039 |
rs259614836 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78891706 | CCACAGTTCCACCTT[C/T]AAGGTTCAGCTCTTC | 106039 |
rs259758029 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78891766 | GGAGATCCATTTAGG[C/T]CCAGTGTTTTGCCTC | 106039 |
rs259766667 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78883764 | ACAGAACTCAGAGTG[A/G]GCTGTGCAGCCCCGT | 106039 |
rs259857588 | in-del | -/GGA | | | intron-variant | Gga1 | GRCm38.p3 | 15:78889635 | ACCTGTAATGAGATG[-/GGA]GGAGGAGGAGGAGGA | 106039 |
rs259935500 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78893025 | TCTGACCCCAAAGAA[C/T]GCATGACCCACACTT | 106039 |
rs259937425 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78882889 | ATCTTGTGATTTTTC[A/G]GGTTTAGGAAAAGCC | 106039 |
rs259941946 | snp | C/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78882546 | TGTGCCACCACTGCC[C/G]GACCGTAGGACACAT | 106039 |
rs259948756 | in-del | -/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78893670 | GGCCCAGCTCTGACG[-/T]GGCAGTGCCCCAGGG | 106039 |
rs260009973 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78881610 | CTCCTCTCTGGGGCA[A/G]GTCCTTCACTGAGCC | 106039 |
rs260293479 | in-del | -/T | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78875356 | ATTCCACACTCTCTC[-/T]GCCCTGTTTCTCAGC | 106039 |
rs260464839 | snp | A/C | | | synonymous-codon | Gga1 | GRCm38.p3 | 15:78889091 | GGTCAACGGTGATGC[A/C]ACAGCCAGCTCCATT | 106039 |
rs260553033 | snp | A/C | | | intron-variant | Gga1 | Mm_Celera | 15:78885478 | ATGCACTGACCCATG[A/C]AGGCATCTGCCTTCA | 106039 |
rs260695719 | snp | C/T | | | intron-variant | Gga1 | Mm_Celera | 15:78887609 | TCTTAAAGGGCTAAG[C/T]GATGTGAGGCTGCCA | 106039 |
rs260785438 | snp | C/T | | | intron-variant | Gga1 | Mm_Celera | 15:78885735 | AGTGCCTCGGTTATC[C/T]GCATGGGCACCCGTC | 106039 |
rs260854202 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880307 | GAGAGCGGAGCAAGG[C/T]ATGTTCTCTGCAGGA | 106039 |
rs260902906 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879685 | CCATCCATCTTGCCT[C/T]TGAGCCCCCGGGAGA | 106039 |
rs260916854 | in-del | -/C | | | utr-variant-3-prime, downstream-variant-500B | Gga1, LOC102632079 | GRCm38.p3 | 15:78894102 | AGGCCCAGCCCTGAA[-/C]CCCCAGCCTGAGGTG | 106039 |
rs260994630 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78891370 | CCAGGGAGGCCCTAG[C/T]GCCACACTGGTGGCT | 106039 |
rs261042284 | in-del | -/A | | | intron-variant | Gga1 | GRCm38.p3 | 15:78881223 | GCAGTGACAGTTGAC[-/A]AAAAACAGTGGCGCT | 106039 |
rs261252976 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Gga1, LOC102632079 | GRCm38.p3 | 15:78894078 | GGGTGAGGGAAGGAG[A/G]GGGGCTGTGAGGCCC | 106039 |
rs261333607 | snp | C/T | | | intron-variant | Gga1 | Mm_Celera | 15:78887296 | AGGCAGGAGACTGCC[C/T]ACCTGTAACCCTGTG | 106039 |
rs261505625 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880573 | AGGCAGATCCAAGTC[C/T]CCTGCGCTGGGTTCC | 106039 |
rs261587369 | in-del | -/G | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78875326 | GAGTGGAGAAAGGGC[-/G]GGGAAGCAGTGTGCA | 106039 |
rs261696696 | in-del | -/TTTT | | | intron-variant | Gga1 | GRCm38.p3 | 15:78884848 | AATTAAAAATAAGTC[-/TTTT]TTTTTTTTTTTTTTT | 106039 |
rs261702964 | snp | G/T | | | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78891179 | TCTTAGCTGCCGAGG[G/T]CCCAAGGTGAAAGTT | 106039 |
rs261733030 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78882378 | ACAATGGACACCTTC[A/G]TAGGACACATGTTTT | 106039 |
rs261977737 | snp | C/T | | | synonymous-codon | Gga1 | GRCm38.p3 | 15:78888456 | CATGCGACCCACACT[C/T]TTCCGACTGGCCAGT | 106039 |
rs261991446 | snp | G/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880361 | CCACTTGGGCCCTCT[G/T]TAAAGAATAGCTAGG | 106039 |
rs262055591 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78884569 | GGCCACCCTGAGCTA[C/T]ATAGGATTCAAAAGG | 106039 |
rs262296246 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78881753 | GCCTTAGCACTCGAG[C/T]TGTTACCACCTGATC | 106039 |
rs262379591 | snp | A/C | | | intron-variant | Gga1 | GRCm38.p3 | 15:78877780 | CGCTCCGCTCGGACC[A/C]TGGCAGCTGCGCGCA | 106039 |
rs262623931 | snp | A/G | | | intron-variant | Gga1 | Mm_Celera | 15:78885803 | CCACACACAGTAACC[A/G]AGGAGCTGGGTTGTA | 106039 |
rs262743600 | snp | A/G | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78876093 | GGTTTTATTTCATTA[A/G]CAATTTTAAAAATAA | 106039 |
rs262798880 | in-del | -/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879856 | TTGTCCACCACCGTA[-/T]TTTTTCTTTTTCTTT | 106039 |
rs262920753 | snp | G/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879478 | CAGGCTCTCTTCCCA[G/T]TGTTCAGTCCCTTAG | 106039 |
rs263770273 | snp | A/G | | | downstream-variant-500B, nc-transcript-variant | Gga1, LOC102632079 | GRCm38.p3 | 15:78895011 | CGAGGACAACCTGCC[A/G]GTGGGGTGCGGTGAG | 106039 |
rs264246020 | snp | A/C | | | intron-variant | Gga1 | GRCm38.p3 | 15:78892416 | GAGCTGGGTAGCCCA[A/C]TACAAAATCACGTGC | 106039 |
rs264250377 | in-del | -/TTT | | | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78890244 | CTGATCTCTTTGGCC[-/TTT]TTTTTTTTTTTTAAG | 106039 |
rs264359983 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78889590 | AAAGAAAGGGCTTGG[C/T]GGGCTGGAGTGGCTC | 106039 |
rs264464771 | in-del | -/GAA | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879540 | GCAGCCTGACCTAAG[-/GAA]GAAGAAGAGATGTTG | 106039 |
rs264500394 | snp | A/C | | | intron-variant | Gga1 | GRCm38.p3 | 15:78883970 | TGGAGCAGCTCCACC[A/C]GGCCTCTTGCAGGGC | 106039 |
rs264529498 | in-del | -/A | | | intron-variant | Gga1 | GRCm38.p3 | 15:78889574 | TGGTTTATTGTGAAC[-/A]AAAGAAAGGGCTTGG | 106039 |
rs264719498 | snp | A/T | | | intron-variant | Gga1 | Mm_Celera | 15:78886024 | AGCTGTGCGTGTGTG[A/T]ACATATGATGTCCTA | 106039 |
rs264776010 | snp | G/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879322 | AGTTTCCTCTTCCCT[G/T]GCTCCTGACTCGGAT | 106039 |
rs264882517 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78889406 | AGAAAAGGCTAGCAG[C/T]GAGGGAGTCTTGGCA | 106039 |
rs265026023 | in-del | -/G | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78875746 | CGTGTTGCTTAGCTT[-/G]CAAGAAGTCCTATTC | 106039 |
rs265043521 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78882630 | CCAGGTTCTCTGCAG[A/G]GGCCATTCAGACCAC | 106039 |
rs265192322 | snp | C/G | | | intron-variant | Gga1 | Mm_Celera | 15:78885195 | CCTATTCCCAGATCC[C/G]TCTCCTGCGACCTCT | 106039 |
rs265202136 | snp | C/T | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78875250 | CCTGCCTGAGTCTAC[C/T]GAGCTGGGAAGACCT | 106039 |
rs265355828 | snp | C/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78878545 | TTCCCAGAGCTCACC[C/G]ATCTGGGGGGGGGGG | 106039 |
rs265397981 | snp | A/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879965 | GCAGGTGCCACATCC[A/T]GGGCCCTAGCCTCTT | 106039 |
rs265431852 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880230 | CTCTGTGCTGTTGCC[C/T]ATCCCTGCATCCCAG | 106039 |
rs266014286 | snp | C/T | | | intron-variant | Gga1 | Mm_Celera | 15:78888314 | ACCCCATCTTACCCC[C/T]GGCCCACCCCAGCTC | 106039 |
rs266105669 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78890314 | TCCTAGTTTCCCCTC[C/T]GAAAACTCCCATTTC | 106039 |
rs386843623 | in-del | -/CCTCCCCTGCTC | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879740 | ATCCCTCCCCTGCTC[-/CCTCCCCTGCTC]TGCCCGTCTTCATAG | 106039 |
rs386922946 | in-del | -/A | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78876860 | GTTAAGAAAAAAAAA[-/A]GACTTAGCCCTTTGC | 106039 |
rs387063162 | in-del | -/AC | | | intron-variant | Gga1 | Mm_Celera | 15:78886484 | CACACACACACACAC[-/AC]GTAAACATTTTTCAA | 106039 |
rs387201267 | in-del | -/GT | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78875952 | TTTGTTTTGGGTTTT[-/GT]TCTGTGTAGCCCTGG | 106039 |
rs387262596 | in-del | -/GCACACGC | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879205 | CACACACACACACAC[-/GCACACGC]ACTGTGGAGGTTGGG | 106039 |
rs387293452 | in-del | -/ACACTTCTGCCTCACAGTGCACA | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880069 | CCCAGAACCATGAGA[-/ACACTTCTGCCTCACAGTGCACA]GCCTGCGTACTGTCC | 106039 |
rs387544549 | in-del | -/A | | | intron-variant | Gga1 | Mm_Celera | 15:78886788 | GCCTCTGCCTCCCAA[-/A]GTGCTGGGATTAAAG | 106039 |
rs387587699 | in-del | -/AGA | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879548 | ACCTAAGGAAGAAGA[-/AGA]GATGTTGCTGGTGTC | 106039 |
rs387636721 | in-del | -/CTCTC | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78876030 | TTCACCTGCCTCTTC[-/CTCTC]AAGTGCTAGGTGGCG | 106039 |
rs387726838 | in-del | -/GTTTTT | | | intron-variant | Gga1 | GRCm38.p3 | 15:78882406 | TTTTTTTTGTTTTTT[-/GTTTTT]TTCAAGACAGGGTTT | 106039 |
rs387780338 | in-del | -/CC | | | intron-variant | Gga1 | GRCm38.p3 | 15:78888716 | GGGAGAACTCTCCCC[-/CC]ATCTCCTAAGCAGAA | 106039 |
rs387879987 | in-del | -/C | | | upstream-variant-2KB | Gga1 | GRCm38.p3 | 15:78875353 | GCATTCCACACTCTC[-/C]CTGCCCTGTTTCTCA | 106039 |
rs579338728 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78884737 | AACACCAGCTCTAGG[A/G]GAGTGGCTGCGTTTT | 106039 |
rs579453109 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78877735 | CTCACGCCCCGCCCC[C/T]CGACCCGGAGGGGCG | 106039 |
rs579654079 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78884917 | GGCTGTCCTGGAACT[C/T]ACTCTGTAGACCAGG | 106039 |
rs579857233 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78878833 | AGGACTGGAACTCAA[A/G]CAGGTCAGGAAGCAG | 106039 |
rs579971603 | snp | A/C | | | intron-variant | Gga1 | GRCm38.p3 | 15:78885003 | GGCGTGCGCCACCAC[A/C]GCCCGGCTAAAAATA | 106039 |
rs580274565 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78878972 | CCCACAATGGGCCTT[C/T]CCCCCTTGATCACTA | 106039 |
rs580424441 | snp | G/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78886681 | ATGTTTGTTTTTTTG[G/T]TTTTTTTTGAGACAG | 106039 |
rs580633958 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78879052 | GAAGCTGCTTTCTCT[A/G]TGATAACTCCAGCTG | 106039 |
rs580834192 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78886795 | CCTCCCAAAGTGCTG[A/G]GATTAAAGGCGTGCG | 106039 |
rs580875859 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78882366 | CTTAACTCACACACA[A/G]TGGACACCTTCATAG | 106039 |
rs581319333 | snp | C/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78889296 | TCATCCCCTAGGCCT[C/G]ATTAGACTTCCAGAA | 106039 |
rs581908654 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78884894 | ACAGGGTTTCTCTGT[A/G]TAGCCCTGGCTGTCC | 106039 |
rs581996207 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78877854 | GTGGCGCAGAGTTAT[C/T]CCGGACCCCCGAAGG | 106039 |
rs582063026 | snp | A/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78884964 | AGATCCGCCTGCCTC[A/T]GCCTCCCAAGTGCTG | 106039 |
rs582585879 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78883703 | TGGACTTTGGTCACA[A/G]TTTGGGTACATATCT | 106039 |
rs582809442 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | Gga1, LOC102632079 | GRCm38.p3 | 15:78894087 | AAGGAGGGGGGCTGT[A/G]AGGCCCAGCCCTGAA | 106039 |
rs583486841 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78878857 | GAAGCAGGAGCTGAT[A/G]CAGAGGCCATGGAGG | 106039 |
rs583773890 | snp | A/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78886603 | TGTATCCCCCAAACA[A/T]ATGTAAGTATGGGTG | 106039 |
rs583993601 | snp | A/C | | | intron-variant, upstream-variant-2KB | Gga1, Mir6955 | GRCm38.p3 | 15:78891389 | ACACTGGTGGCTATT[A/C]GCCTCATCTGCCCAC | 106039 |
rs584032774 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78878976 | CAATGGGCCTTTCCC[C/T]CTTGATCACTAATTG | 106039 |
rs584135935 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78886735 | GTCCTGGAACTCACC[C/T]TGTAGATCAGGCTGG | 106039 |
rs584196899 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78888286 | CAGCTCACTCCCAGC[C/T]CACTCCCAGCCCACC | 106039 |
rs584395670 | snp | A/C | | | intron-variant | Gga1 | GRCm38.p3 | 15:78880903 | AGGTCAGTGCTCAGG[A/C]GTGGGGGTGTCCAGC | 106039 |
rs584977065 | snp | A/G | | | intron-variant, downstream-variant-500B | Gga1, Mir6955 | GRCm38.p3 | 15:78892340 | CATGGGAGGATGCTG[A/G]GGCAAGGAGTGGGGG | 106039 |
rs585065946 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78884056 | GGCCGAGCAGTGTCC[A/G]AGAAGTCCCCTTCTG | 106039 |
rs585113999 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78884898 | GGTTTCTCTGTGTAG[C/T]CCTGGCTGTCCTGGA | 106039 |
rs585718081 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78878817 | ATCACCAAAGGATGT[C/T]AGGACTGGAACTCAA | 106039 |
rs585862346 | snp | C/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78884969 | CGCCTGCCTCTGCCT[C/G]CCAAGTGCTGGGATT | 106039 |
rs586245235 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78886768 | TCGAACTCAGAAATC[C/T]GCCTGCCTCTGCCTC | 106039 |
rs586741430 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78881029 | TACTGACTCCCTCTG[C/T]TCCTGCAGACAGAGC | 106039 |
rs586767356 | snp | A/G | | | intron-variant | Gga1 | GRCm38.p3 | 15:78878936 | TATAGAACCAAGACT[A/G]CCAGCCCAGAGATGG | 106039 |
rs586942627 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78888331 | GCCCACCCCAGCTCA[C/T]ACCCAGCCCATCCAA | 106039 |
rs587483134 | snp | A/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78886608 | CCCCCAAACATATGT[A/T]AGTATGGGTGTGTAT | 106039 |
rs587564210 | snp | C/T | | | intron-variant | Gga1 | GRCm38.p3 | 15:78878989 | CCCCTTGATCACTAA[C/T]TGAGAAAATGCCTTA | 106039 |