SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13459622 | snp | A/G | | | utr-variant-3-prime | Wdsub1 | Mm_Celera | 2:59852539 | cggccaaggctacac[A/G]gagaaaccctgtctc | 72137 |
rs13459623 | snp | A/G | | | utr-variant-3-prime | Wdsub1 | Mm_Celera | 2:59852627 | ttaatcccagcactc[A/G]ggaggcagagacagg | 72137 |
rs13459624 | snp | A/G | | | utr-variant-3-prime | Wdsub1 | Mm_Celera | 2:59852577 | gttccaggacagccc[A/G]gtttatagggcaagt | 72137 |
rs13459625 | snp | A/G | | | utr-variant-3-prime | Wdsub1 | Mm_Celera | 2:59852664 | CTGTAAATTATGAgc[A/G]gggcagtggtggtgc | 72137 |
rs13459626 | snp | A/G | | | utr-variant-3-prime | Wdsub1 | Mm_Celera | 2:59852646 | gcagtggtggtgccc[A/G]cctttaatcccagca | 72137 |
rs13459627 | snp | A/G | | | utr-variant-3-prime | Wdsub1 | Mm_Celera | 2:59852659 | AATTATGAgcagggc[A/G]gtggtggtgcccacc | 72137 |
rs13459628 | snp | A/G | | | utr-variant-3-prime | Wdsub1 | Mm_Celera | 2:59852555 | agggcaagtctcagg[A/G]cggccaaggctacac | 72137 |
rs13459629 | snp | A/G | | | utr-variant-3-prime | Wdsub1 | Mm_Celera | 2:59852631 | acctttaatcccagc[A/G]ctcaggaggcagaga | 72137 |
rs13459630 | snp | A/G | 0.277778 | 0.248452 | synonymous-codon, utr-variant-5-prime | Wdsub1 | GRCm38.p3 | 2:59876773 | TGTCACTGGCTCCTC[A/G]GGCGGGGACTTGACA | 72137 |
rs13459631 | snp | A/C/G | 0.165289 | 0.235211 | missense, intron-variant | Wdsub1 | GRCm38.p3 | 2:59878167 | GCTGCCGATGGATCC[A/C/G]TTGCTTTGTGGAATG | 72137 |
rs28021751 | snp | A/G | 0.260355 | 0.249785 | upstream-variant-2KB | Wdsub1 | Mm_Celera | 2:59884607 | AAGTGCTTCCCCTGG[A/G]ACCCAAGTGGCATGT | 72137 |
rs28021752 | snp | A/G | 0.277778 | 0.248452 | upstream-variant-2KB | Wdsub1 | Mm_Celera | 2:59884566 | CACATAGACTTTTTC[A/G]GTACATTCCAGATCC | 72137 |
rs28021753 | snp | A/G | 0.297521 | 0.245442 | upstream-variant-2KB | Wdsub1 | Mm_Celera | 2:59884534 | AAGTGCCAGGGGCTT[A/G]AGACCCAAGCTTTTA | 72137 |
rs28021754 | snp | C/G | 0.165289 | 0.235211 | upstream-variant-2KB | Wdsub1 | Mm_Celera | 2:59884201 | CCTGAGTCCTTGAGA[C/G]CAGATGGTAAAAGTC | 72137 |
rs28021755 | snp | C/T | 0.21875 | 0.248039 | upstream-variant-2KB | Wdsub1 | Mm_Celera | 2:59884032 | GGAGAGGCAAGCCCT[C/T]TCTGGTAGCTTGTCT | 72137 |
rs28021756 | snp | C/T | 0.165289 | 0.235211 | upstream-variant-2KB | Wdsub1 | Mm_Celera | 2:59884001 | AGCACGTTCACCCCA[C/T]GGGACAGGTAGTTTG | 72137 |
rs28021757 | snp | A/G | 0.142012 | 0.225474 | upstream-variant-2KB | Wdsub1 | Mm_Celera | 2:59883526 | TTTCCTTTGAGGCCC[A/G]TTGCAAGGATGCAGC | 72137 |
rs28021758 | snp | A/T | 0.152778 | 0.230321 | upstream-variant-2KB | Wdsub1 | Mm_Celera | 2:59883511 | GTCTGTCACGCCTTC[A/T]TTCCTTTGAGGCCCG | 72137 |
rs28021759 | snp | C/T | 0.152778 | 0.230321 | upstream-variant-2KB | Wdsub1 | Mm_Celera | 2:59883501 | GTGGATGTGTGTCTG[C/T]CACGCCTTCTTTCCT | 72137 |
rs28021760 | snp | C/G | 0.46875 | 0.121031 | upstream-variant-2KB | Wdsub1 | Mm_Celera | 2:59883473 | GAGCCCAGACCATGT[C/G]ATCCCAGATTCTGTG | 72137 |
rs28021761 | snp | C/T | 0.152778 | 0.230321 | upstream-variant-2KB | Wdsub1 | Mm_Celera | 2:59883390 | GTTGAACTGTAACCC[C/T]TCTCTGTGTCCAACT | 72137 |
rs28021762 | snp | A/T | 0.152778 | 0.230321 | upstream-variant-2KB | Wdsub1 | Mm_Celera | 2:59883268 | TCCTCCTGGATGTTT[A/T]CCGCCTGAAGACTGG | 72137 |
rs28021763 | snp | C/G | 0.152778 | 0.230321 | upstream-variant-2KB | Wdsub1 | Mm_Celera | 2:59883244 | GCAGAAATGTCCTCT[C/G]TAGCTTTGTCCTCCT | 72137 |
rs28021764 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB | Wdsub1 | Mm_Celera | 2:59882822 | TGCCGAATGGTAGTT[C/T]AACTTTTTTGCTCAC | 72137 |
rs28021765 | snp | A/C | 0.277778 | 0.248452 | upstream-variant-2KB | Wdsub1 | Mm_Celera | 2:59882698 | GGCAGCTCCGGTAGG[A/C]CGGTTCCCTGTGGGC | 72137 |
rs28021766 | snp | C/G | 0.486111 | 0.0821678 | utr-variant-5-prime, upstream-variant-2KB | Wdsub1 | Mm_Celera | 2:59882578 | TCACTAGGCAGAGCC[C/G]GACTCACTGGGTCAC | 72137 |
rs28021767 | snp | A/C | 0.18 | 0.24 | intron-variant | Wdsub1 | Mm_Celera | 2:59882174 | AAGCAGAAACACTCC[A/C]ACAGGTTCTCGGAAA | 72137 |
rs28021768 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Wdsub1 | Mm_Celera | 2:59882007 | TCCCTAAGAAACAGA[C/T]GTGACCTCGACTTGT | 72137 |
rs28021769 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Wdsub1 | Mm_Celera | 2:59881970 | AAAACCAACAAACGA[A/G]TAACAATCGCGGCTG | 72137 |
rs28021770 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Wdsub1 | Mm_Celera | 2:59879984 | GGACTTCACCTATTT[G/T]TGTTACGTTTCTGTT | 72137 |
rs28021771 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Wdsub1 | Mm_Celera | 2:59879960 | ACTGCCCTAGACACA[C/T]GCCTGGTGGGACTTC | 72137 |
rs28021772 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Wdsub1 | Mm_Celera | 2:59879952 | TAGCTAATACTGCCC[C/T]AGACACATGCCTGGT | 72137 |
rs28021773 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Wdsub1 | Mm_Celera | 2:59879794 | CAGAGTACAGATGTT[C/T]GGGTACTGGGGCAGA | 72137 |
rs28021774 | snp | A/C | 0.18 | 0.24 | intron-variant | Wdsub1 | Mm_Celera | 2:59879759 | TTTAAAGAGCAGAGT[A/C]TCAAGGGCTGCTCCA | 72137 |
rs28021775 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Wdsub1 | Mm_Celera | 2:59879697 | GTCTAGCTTGGAATA[C/T]ACGTGGAAGCCAGGA | 72137 |
rs28021776 | snp | A/C/T | 0.277778 | 0.248452 | intron-variant | Wdsub1 | GRCm38.p3 | 2:59879602 | GCTTTCTGCTCTTAC[A/C/T]GAGTCCTTTCTAATT | 72137 |
rs28021777 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Wdsub1 | Mm_Celera | 2:59879210 | CCTGATCTCTGGATC[C/T]GTTCCTTCTGGAAAT | 72137 |
rs28021778 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Wdsub1 | Mm_Celera | 2:59879027 | TAGCTCATAAAAACA[C/T]ACGGTCTGATCCCTT | 72137 |
rs28021779 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Wdsub1 | Mm_Celera | 2:59879008 | AAATCCAAATTCCTT[C/T]CGATAGCTCATAAAA | 72137 |
rs28021780 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Wdsub1 | Mm_Celera | 2:59877710 | GCTAGGTTAACCCTT[C/G]AACACCGCTTAAAAG | 72137 |
rs28021781 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Wdsub1 | Mm_Celera | 2:59877676 | CCAGGCACCCATCCT[C/T]TCTGCGCTGTCTGGT | 72137 |
rs28021782 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Wdsub1 | Mm_Celera | 2:59877652 | TCACCAGTGGCAAGC[C/T]CTCCTTAGCCAGGCA | 72137 |
rs28021783 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Wdsub1 | Mm_Celera | 2:59877570 | CAAACTGGTGAGCCC[A/T]GGGCAATTAGAGCGC | 72137 |
rs28021784 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Wdsub1 | Mm_Celera | 2:59877488 | AAAACCCACATGTGT[A/G]CCACAGTTCTCCTGG | 72137 |
rs28021785 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Wdsub1 | Mm_Celera | 2:59877444 | TACTAAGACTCTGCG[C/T]CTCAGCATCAAACAA | 72137 |
rs28021786 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Wdsub1 | Mm_Celera | 2:59877377 | TTTCTTACTGAAAAG[A/C]CATGCTATTAAAATA | 72137 |
rs28021787 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Wdsub1 | Mm_Celera | 2:59877056 | CAATCTCGTATCTTT[A/G]TATTTTCATAGCAAG | 72137 |
rs28021788 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Wdsub1 | Mm_Celera | 2:59876648 | GGGAGCCCGCGCTTA[A/G]AAGAGTGAGCCAACC | 72137 |
rs28021789 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Wdsub1 | Mm_Celera | 2:59876588 | GCCCTCGGTACTAAC[A/G]ATGACGTGGAAACTC | 72137 |
rs28021790 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdsub1 | Mm_Celera | 2:59876505 | CTTTTCATGTTAGAG[C/T]TCTTCACGATTCACG | 72137 |
rs28021791 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Wdsub1 | Mm_Celera | 2:59875175 | ACAAGTGCATGCCTT[A/C]AAGATGTGGAGAAGG | 72137 |
rs28021792 | snp | C/T | 0.152778 | 0.230321 | missense | Wdsub1 | Mm_Celera | 2:59874251 | TACCTAAGACACGGG[C/T]AATAGTAACAGCCCA | 72137 |
rs28021793 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdsub1 | Mm_Celera | 2:59873532 | TATGTAGCCCTATGT[C/T]CAACACAAACATGCT | 72137 |
rs28021794 | snp | A/G | 0.18 | 0.24 | intron-variant | Wdsub1 | Mm_Celera | 2:59872933 | GGGGAGTGGATACAA[A/G]CTAACCATGCTAAAG | 72137 |
rs28021795 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Wdsub1 | Mm_Celera | 2:59872449 | AACAAAAACTCCTAG[C/T]GAGGTAAAACTAAGC | 72137 |
rs28021796 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Wdsub1 | Mm_Celera | 2:59870916 | CACCCTGGTATGGTC[A/G]CACACTCATGCCCAT | 72137 |
rs28021797 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdsub1 | Mm_Celera | 2:59870847 | CAGAGCCCTCACCAG[C/T]ACCAGGGTCACCTGC | 72137 |
rs28021798 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Wdsub1 | Mm_Celera | 2:59870494 | ACAGAATCTGTAAAA[G/T]TACAGAGCGGGCGAT | 72137 |
rs28021799 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Wdsub1 | Mm_Celera | 2:59868882 | TAAGTCTTGAGTGTG[C/T]GTTAGACTGCCATAG | 72137 |
rs28021800 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Wdsub1 | Mm_Celera | 2:59868801 | GGAAAAGATTCAACA[A/G]TGTCGGCCAGGTGTT | 72137 |
rs28021801 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Wdsub1 | Mm_Celera | 2:59868471 | GCTCTGCCCATTAGC[C/T]TGTTCCTCAGCCAGG | 72137 |
rs28021802 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Wdsub1 | Mm_Celera | 2:59868434 | ATGAGACAGCCACAC[A/C]CGTGTTTAACCTCAC | 72137 |
rs28021803 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Wdsub1 | Mm_Celera | 2:59868354 | ACCAGGCCCTAGAGT[A/C]ATCATCATGGACATC | 72137 |
rs28021804 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Wdsub1 | Mm_Celera | 2:59867918 | TATTTCAAATCACTC[A/G]CTCATTTGTATATCC | 72137 |
rs28021805 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Wdsub1 | Mm_Celera | 2:59867746 | TCCCCTTCCATGCGC[A/T]TTGGTTTTCACTGTC | 72137 |
rs28021806 | snp | G/T | 0.165289 | 0.235211 | intron-variant | Wdsub1 | Mm_Celera | 2:59866751 | AGTCTGAGTTCCATG[G/T]AAGTCTCTCGTGCCT | 72137 |
rs28021807 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Wdsub1 | Mm_Celera | 2:59866732 | GCTGTACTGGGATAA[C/T]GTTAGTCTGAGTTCC | 72137 |
rs28021808 | snp | A/C | 0.197531 | 0.244432 | intron-variant | Wdsub1 | Mm_Celera | 2:59866138 | GTTTAGGGAAAGGCA[A/C]TGGGGTCATGTGGCT | 72137 |
rs28021809 | snp | G/T | 0.197531 | 0.244432 | intron-variant | Wdsub1 | Mm_Celera | 2:59866083 | GATTTTGGCCTTCTG[G/T]TTCCTTCCTACTTAG | 72137 |
rs28021810 | snp | A/T | 0.197531 | 0.244432 | intron-variant | Wdsub1 | Mm_Celera | 2:59866069 | TTTTCAGGAATAGGG[A/T]TTTTGGCCTTCTGTT | 72137 |
rs28021811 | snp | C/T | 0.18 | 0.24 | intron-variant | Wdsub1 | Mm_Celera | 2:59865938 | TAGCGTTAAGTCACC[C/T]TCTGCTAGTCACTGT | 72137 |
rs28021812 | snp | G/T | 0.197531 | 0.244432 | intron-variant | Wdsub1 | Mm_Celera | 2:59865914 | AGGCTGAGTTTTAGG[G/T]AGTGTAGCTAGCGTT | 72137 |
rs28021813 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdsub1 | Mm_Celera | 2:59865891 | TAATGAGAGTAAGGG[A/G]AAGACAGAGGCTGAG | 72137 |
rs28021814 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Wdsub1 | GRCm38.p3 | 2:59865423 | ATTCAGCCAACCCTG[A/C]TGTATGGAAGCCACA | 72137 |
rs28021815 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Wdsub1 | Mm_Celera | 2:59865368 | TCGCATATGCAGGTC[C/T]CTAAACCCACCTGTA | 72137 |
rs28021816 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Wdsub1 | Mm_Celera | 2:59865341 | TATTTGTCCAAGGCT[A/T]TGGTAACTTACTCGC | 72137 |
rs28021817 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Wdsub1 | Mm_Celera | 2:59864856 | GAAAATTACCAAATA[C/T]TGTATATGCCAGACA | 72137 |
rs28021818 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Wdsub1 | Mm_Celera | 2:59864709 | CTCTGCTCAGTAGGC[A/G]ACTGAACACTGACAG | 72137 |
rs28021819 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Wdsub1 | Mm_Celera | 2:59864020 | ATTCAGCCAACCCTG[A/C]TGTATGGAAGCCACC | 72137 |
rs28021820 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Wdsub1 | Mm_Celera | 2:59863965 | TCGCATATGCAGGTC[C/T]CTAAACCCACCTGTA | 72137 |
rs28021821 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Wdsub1 | Mm_Celera | 2:59863545 | GACAGGTGTATTTAG[C/T]GAGGAGTAGCTCATG | 72137 |
rs28021822 | snp | C/T | 0.142012 | 0.225474 | synonymous-codon, missense | Wdsub1 | Mm_Celera | 2:59862672 | CACTGTCTTGTCCAT[C/T]GAACCAGTAGCAAGT | 72137 |
rs28021823 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Wdsub1 | Mm_Celera | 2:59862413 | TTAGGCTTGGGAGTA[C/T]AGCTCTGAGGTAGAG | 72137 |
rs28021824 | snp | C/T | 0.42 | 0.183303 | intron-variant | Wdsub1 | Mm_Celera | 2:59861894 | AAATGCTATTCTTTA[C/T]GAACTTCTTCTTCAC | 72137 |
rs28021825 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdsub1 | Mm_Celera | 2:59856411 | GAGTCCCTTCTAGCT[C/T]CTATTGTATTTAGTT | 72137 |
rs28021826 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Wdsub1 | Mm_Celera | 2:59855710 | CATCCTCACACCAGA[C/T]GGTTCAAGCTGTCCT | 72137 |
rs28021827 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Wdsub1 | Mm_Celera | 2:59854506 | GCTCCGTCCTTCCCA[C/T]GACTGAAGACCGACA | 72137 |
rs28021828 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Wdsub1 | Mm_Celera | 2:59854261 | GCCATGATACTGTGC[C/G]TACTGCTCTGTTGTA | 72137 |
rs28021829 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdsub1 | Mm_Celera | 2:59853626 | CTTGTTTCTCTCTGT[A/G]CTAAATGCACACCGG | 72137 |
rs28021830 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Wdsub1 | Mm_Celera | 2:59853217 | AAGCACAGCGGCTGA[C/G]ACCAGAACCCTGGTG | 72137 |
rs28021831 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdsub1 | Mm_Celera | 2:59853211 | CCCCTGAAGCACAGC[A/G]GCTGACACCAGAACC | 72137 |
rs28021832 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdsub1 | Mm_Celera | 2:59853093 | CCGCGTCCTAAATAC[A/G]CCAGCCACAGCAGCT | 72137 |
rs28021833 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Wdsub1 | Mm_Celera | 2:59853079 | TCTCTTTGCCTGTAC[C/G]GCGTCCTAAATACAC | 72137 |
rs28021834 | snp | C/G | 0.132653 | 0.220748 | missense | Wdsub1 | Mm_Celera | 2:59852824 | TCTCGTGCGTCTCCA[C/G]CCATCGGTTGATGGC | 72137 |
rs28021835 | snp | A/G | 0.132653 | 0.220748 | utr-variant-3-prime | Wdsub1 | Mm_Celera | 2:59852748 | TGATGGCTGCTTAGC[A/G]TTTTGAATCATTTGC | 72137 |
rs28021836 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime | Wdsub1 | Mm_Celera | 2:59852395 | AGTTTTATTTCTACA[C/T]AGTTTCTCATTATTG | 72137 |
rs28021837 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B | Wdsub1 | Mm_Celera | 2:59852333 | ACAGAATATGGCCTA[C/T]GCCCAATAAGAACAC | 72137 |
rs28021838 | snp | C/T | 0.32 | 0.24 | downstream-variant-500B | Wdsub1 | Mm_Celera | 2:59852122 | GACAATGGAGAAAAG[C/T]CTTATGCTGTACAAA | 72137 |
rs29538511 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Wdsub1 | Mm_Celera | 2:59883283 | ACCGCCTGAAGACTG[A/G]TCCCCCACAGAGACT | 72137 |
rs29583736 | snp | G/T | 0.375 | 0.216506 | intron-variant | Wdsub1 | Mm_Celera | 2:59864548 | AAATAAGTCTATTTT[G/T]TTTCTACTCTTAGAA | 72137 |