SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3676814 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Psmd14 | Mm_Celera | 2:61787838 | AATTAAATTCTTATG[C/T]TCCAAGTTTTCAATC | 59029 |
rs4223187 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Psmd14 | Mm_Celera | 2:61799794 | GACTTTCAGTGGGTA[A/T]TTTTTTTTCTAGCTT | 59029 |
rs4223188 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Psmd14 | Mm_Celera | 2:61799870 | TGAATGATAAAGTAT[G/T]TGTAAATTTAGGCTT | 59029 |
rs4223189 | snp | C/T | 0.484143 | 0.0876178 | utr-variant-3-prime | Psmd14 | Mm_Celera | 2:61800083 | TGTATTTAAATAAAG[C/T]GACGTAGAGAGCTGT | 59029 |
rs6171348 | snp | A/T | 0.5 | 0 | intron-variant | Psmd14 | Mm_Celera | 2:61768758 | CTCTATTTTCTTCTT[A/T]TTAAAAATNATACAT | 59029 |
rs6171367 | snp | A/C | 0.5 | 0 | intron-variant | Psmd14 | Mm_Celera | 2:61768767 | CTTCTTNTTAAAAAT[A/C]ATACATATAAATTAT | 59029 |
rs6192582 | snp | A/G | 0.5 | 0 | intron-variant | Psmd14 | Mm_Celera | 2:61730647 | TAAAAACAGTAAGTA[A/G]TACTTTCCAAGCGGA | 59029 |
rs13476535 | snp | A/G | 0.264514 | 0.249578 | intron-variant | Psmd14 | Mm_Celera | 2:61756786 | AAAAGAGGAATGGCC[A/G]AATGTCACTTTTGTT | 59029 |
rs28038902 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Psmd14, Tbr1 | Mm_Celera | 2:61800872 | TAGTGTAAATGAATA[C/T]CATGAGTTTGGAAAC | 59029 |
rs28038903 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime | Psmd14 | Mm_Celera | 2:61800129 | TGTATCGTCCTTCTT[C/T]GTTCCCAATGCTCAC | 59029 |
rs28038904 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Psmd14 | Mm_Celera | 2:61799058 | CTAGATAATAGTAAC[A/G]TAGTCTAGTCGATGG | 59029 |
rs28038905 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Psmd14 | Mm_Celera | 2:61798589 | CACTAAATAAATTAC[C/T]TTCTGAAGCTGTGGT | 59029 |
rs28038906 | snp | A/G | 0.32 | 0.24 | intron-variant | Psmd14 | Mm_Celera | 2:61798317 | GTAGATAGCTGATAA[A/G]TGAGTTACCAATTCA | 59029 |
rs28038907 | snp | G/T | 0.32 | 0.24 | intron-variant | Psmd14 | Mm_Celera | 2:61797877 | TCATGTAGCCATTTT[G/T]ACAGGTATATTTTTG | 59029 |
rs28038908 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Psmd14 | Mm_Celera | 2:61797690 | GTCGTAGTGAAAACA[A/G]TTACTAAACAAGTTA | 59029 |
rs28038909 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Psmd14 | Mm_Celera | 2:61797671 | TCTCAACCGATGACG[C/T]GCTGTCGTAGTGAAA | 59029 |
rs28038910 | snp | A/G | 0.32 | 0.24 | intron-variant | Psmd14 | Mm_Celera | 2:61797639 | CTCTTTGCTGCTTGT[A/G]GAGACTAAATCATGA | 59029 |
rs28038911 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Psmd14 | Mm_Celera | 2:61797314 | TGAATGGAGATTATG[A/G]TCACCTTGCTTCGGT | 59029 |
rs28038912 | snp | A/G | 0.32 | 0.24 | intron-variant | Psmd14 | Mm_Celera | 2:61797273 | AAAATTACTTTTCCA[A/G]CAAATTGCTTGAATA | 59029 |
rs28038913 | snp | A/C | 0.32 | 0.24 | intron-variant | Psmd14 | Mm_Celera | 2:61796948 | TGTCGAGATTAACTT[A/C]TAATGTATGTATTAG | 59029 |
rs28038914 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Psmd14 | Mm_Celera | 2:61796702 | ATTGAGGGTGTGCTG[C/T]ACCATTCAGGCCTAG | 59029 |
rs28038915 | snp | C/T | 0.32 | 0.24 | intron-variant | Psmd14 | Mm_Celera | 2:61796677 | ATGCTTTGTGAAGAG[C/T]GCTGTGGTTATTGAG | 59029 |
rs28038916 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Psmd14 | Mm_Celera | 2:61796649 | CTGTTCACTGCAGAC[C/T]TTTTAGGTTCAGATG | 59029 |
rs28038917 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Psmd14 | Mm_Celera | 2:61796623 | TGTCTGGAGGCTGTA[A/G]TGTACCCGCACTGTT | 59029 |
rs28038918 | snp | C/G | 0.42 | 0.183303 | intron-variant | Psmd14 | Mm_Celera | 2:61796559 | ATACAGGTTCTGTCT[C/G]GAGGCTGTAATATAA | 59029 |
rs28038919 | snp | C/G | 0.260355 | 0.249785 | intron-variant, nc-transcript-variant | Psmd14, LOC105244183 | Mm_Celera | 2:61794237 | GTCAAAAGTTTTGTT[C/G]TTCTTCATAGTCAAG | 59029 |
rs28038920 | snp | A/G | 0.336735 | 0.234472 | intron-variant, nc-transcript-variant | Psmd14, LOC105244183 | Mm_Celera | 2:61793909 | GCTTGAGAATTCCTT[A/G]GTAAAGATAATGTAA | 59029 |
rs28038921 | snp | A/C | 0.42 | 0.183303 | intron-variant, nc-transcript-variant | Psmd14, LOC105244183 | Mm_Celera | 2:61793687 | TGCTCGCCCGGTGTC[A/C]GCATTGCTGCTGGCT | 59029 |
rs28038922 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Psmd14, LOC105244183 | Mm_Celera | 2:61791456 | TCCCACTTAAATCTC[A/G]TTCTCACAGAGCCAC | 59029 |
rs28038923 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Psmd14, LOC105244183 | Mm_Celera | 2:61791407 | CACTATCACTGCCTT[A/T]GTTCCCAGCTAGTCT | 59029 |
rs28038924 | snp | C/T | 0.260355 | 0.249785 | intron-variant, upstream-variant-2KB | Psmd14, LOC105244183 | Mm_Celera | 2:61790000 | CTGTTGTTCCAGTTG[C/T]CTTGAATGTCATAGA | 59029 |
rs28038925 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Psmd14, LOC105244183 | Mm_Celera | 2:61789452 | ATGGATGTTGGCAAT[C/T]TGAAGATACTACCAC | 59029 |
rs28038926 | snp | C/T | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Psmd14, LOC105244183 | Mm_Celera | 2:61788968 | CTGATCATCTTTCTG[C/T]TCTATGTTCACTGTA | 59029 |
rs28038927 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Psmd14, LOC105244183 | Mm_Celera | 2:61788385 | ATTTTCAGAACTGTT[C/T]AGTCAAGAATGATGT | 59029 |
rs28038928 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Psmd14 | Mm_Celera | 2:61786890 | TTGTGTAGTGACAGT[A/G]GTAATGGAGGCATTG | 59029 |
rs28038929 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Psmd14 | Mm_Celera | 2:61786355 | GCTTGGTATGATGTC[C/T]AGTGCTGAAGAGGAA | 59029 |
rs28038930 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Psmd14 | Mm_Celera | 2:61786347 | TGTAAAGAGCTTGGT[A/G]TGATGTCTAGTGCTG | 59029 |
rs28038931 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Psmd14 | Mm_Celera | 2:61784704 | TCAGGAAGTTTGTGA[A/G]TTTGAAGTCAAACTG | 59029 |
rs28038932 | snp | A/G | 0.32 | 0.24 | intron-variant | Psmd14 | Mm_Celera | 2:61784422 | GACATTTAGAGAAAC[A/G]CAGAAGTGCAGCAGA | 59029 |
rs28038933 | snp | A/G | 0.32 | 0.24 | intron-variant | Psmd14 | Mm_Celera | 2:61784067 | CATCGAGCAGGCTGC[A/G]CTGTGAGGTTTGTTT | 59029 |
rs28038934 | snp | A/G | 0.32 | 0.24 | intron-variant | Psmd14 | Mm_Celera | 2:61783758 | ATACATAAGAGGTGG[A/G]TGTATCATGCATAAG | 59029 |
rs28038935 | snp | G/T | 0.32 | 0.24 | intron-variant | Psmd14 | Mm_Celera | 2:61783203 | GCGTACTCTTGAGTT[G/T]TAAATTTTTCTTCTG | 59029 |
rs28038936 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Psmd14 | Mm_Celera | 2:61783130 | AATTAACAAGAAGGG[A/G]AACCCAGATTAATGT | 59029 |
rs28038937 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Psmd14 | Mm_Celera | 2:61783083 | CTCATTGCTAGTTTG[A/G]AGACTTGCCTGGACA | 59029 |
rs28038938 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Psmd14 | Mm_Celera | 2:61782848 | CAGGGCTCAGTTGAT[A/G]AGTGTCTGTTGCACA | 59029 |
rs28038939 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Psmd14 | Mm_Celera | 2:61782814 | TGGAAACGGTAAAGA[C/T]CAAGCTTCTGGGTCT | 59029 |
rs28038940 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Psmd14 | Mm_Celera | 2:61782758 | TCTGATAGGTGAGAT[G/T]ATGATTTCTTGTCAC | 59029 |
rs28038941 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Psmd14 | Mm_Celera | 2:61781506 | CCCGAGTTAGAAAGT[A/G]GTGGGTATTTGGTTA | 59029 |
rs28038942 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Psmd14 | Mm_Celera | 2:61781361 | TTACTCCTCTGTCAT[A/G]TGCACATAGAGCGAA | 59029 |
rs28038943 | snp | A/T | 0.32 | 0.24 | intron-variant | Psmd14 | Mm_Celera | 2:61780857 | CTGGCCCCTGGCTTT[A/T]TTGGGTGTAACCATT | 59029 |
rs28038944 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Psmd14 | Mm_Celera | 2:61780325 | AATCCATAGCAGATA[A/G]TGTATGGAAATTTAA | 59029 |
rs28038945 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Psmd14 | Mm_Celera | 2:61780316 | CCCCTGATAAATCCA[C/T]AGCAGATAGTGTATG | 59029 |
rs28038946 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Psmd14 | Mm_Celera | 2:61780027 | TGAGGCAGCTGAATC[C/T]AGAAAACTGAGCTGT | 59029 |
rs28038947 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Psmd14 | Mm_Celera | 2:61779692 | TTATTTTATACCTGG[A/G]ACATTTGACCATCAG | 59029 |
rs28038948 | snp | C/T | 0.32 | 0.24 | intron-variant | Psmd14 | Mm_Celera | 2:61779654 | CAGTGCTACTTGCTT[C/T]TGGTATAATACACAA | 59029 |
rs28038949 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Psmd14 | Mm_Celera | 2:61779059 | CTTGTTTTCTTTATC[C/T]TTATTGGCACATGCC | 59029 |
rs28038950 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Psmd14 | Mm_Celera | 2:61778992 | TAGAACTTGTACTTA[C/G]ATATTTAGTCCAACA | 59029 |
rs28038951 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Psmd14 | Mm_Celera | 2:61777837 | CATTAATAGTTCACC[A/G]TGGTCCAGCCTTGAT | 59029 |
rs28038952 | snp | A/C | 0.375 | 0.216506 | intron-variant | Psmd14 | Mm_Celera | 2:61777616 | ACAAGTCTTTATTGT[A/C]TGTAGGAAATTATGT | 59029 |
rs28038953 | snp | A/T | 0.5 | 0 | intron-variant | Psmd14 | Mm_Celera | 2:61765485 | AGAAGAATGATTAAA[A/T]ATGCTGACTGACTCT | 59029 |
rs28038954 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Psmd14 | Mm_Celera | 2:61765457 | ACCATTCATGTATTT[A/G]GAGTGAGGACCCAGA | 59029 |
rs28038955 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Psmd14 | Mm_Celera | 2:61764800 | TGTGTTGTTTCTCTC[C/T]TCTCATCATGCATTG | 59029 |
rs28038956 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Psmd14 | Mm_Celera | 2:61764285 | CCAAGTGGTTTTTTT[C/T]CTCCTTCAAGCTAAG | 59029 |
rs28038957 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Psmd14 | Mm_Celera | 2:61764136 | TTGGGCTATTCTGTT[C/T]CTCTGTTTAACATCT | 59029 |
rs28038958 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Psmd14 | Mm_Celera | 2:61764082 | CCACCAATCAGAAAA[C/T]GGCCTTGTATTAAGA | 59029 |
rs28038959 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Psmd14 | Mm_Celera | 2:61763211 | ACTTAGGCTTCTGAT[C/G]TTGGAAGAAAGCCTT | 59029 |
rs28038960 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Psmd14 | Mm_Celera | 2:61762861 | TAAATGCTTGCTTGA[A/T]GATGTGAGATAGGCT | 59029 |
rs28038961 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Psmd14 | Mm_Celera | 2:61761110 | GTGAGTATTACTTAT[A/G]TTGGCTGTTGCATAT | 59029 |
rs28038962 | snp | C/T | 0.391111 | 0.206368 | synonymous-codon | Psmd14 | Mm_Celera | 2:61760989 | GATGTTAAAACATGG[C/T]CGTGCTGGAGTGCCT | 59029 |
rs28038963 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Psmd14 | Mm_Celera | 2:61760452 | AAAGTTGTCAGGATA[C/T]TGAGTTTTAACTGTT | 59029 |
rs28038964 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Psmd14 | Mm_Celera | 2:61759912 | GTGCAGCTCACTGTG[A/G]CACTCAGTAGAGATT | 59029 |
rs28038965 | snp | A/G | 0.32 | 0.24 | intron-variant | Psmd14 | Mm_Celera | 2:61759305 | AAATAAAAGCAGTCA[A/G]AGCAGTCGGAAACAT | 59029 |
rs28038966 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Psmd14 | Mm_Celera | 2:61758643 | AAGGCTAAAGTTTAA[C/G]TTCCACAAATGTATC | 59029 |
rs28038967 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Psmd14 | Mm_Celera | 2:61758431 | TGATTATAAATTACA[C/T]CCAACAAAGGCAGGG | 59029 |
rs28038968 | snp | C/T | 0.32 | 0.24 | intron-variant | Psmd14 | Mm_Celera | 2:61758392 | AAATATTACTGAGTT[C/T]TTGCTATGTGCTTTG | 59029 |
rs28038969 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Psmd14 | Mm_Celera | 2:61758217 | CTAATGCAGGGCTTT[C/T]TGTAGTATGATTCTG | 59029 |
rs28038970 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Psmd14 | Mm_Celera | 2:61758047 | AATAGGTGGTCCACA[A/C]CTGAGCCATCAAGGA | 59029 |
rs28038971 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Psmd14 | Mm_Celera | 2:61757917 | TATCCTAGTTTTTCG[A/T]CCCTCTGCTTTTTTC | 59029 |
rs28038972 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Psmd14 | Mm_Celera | 2:61757239 | TCATTGATTTGTCAG[C/T]CAACAGTTTTATTTC | 59029 |
rs28038973 | snp | A/G | 0.32 | 0.24 | intron-variant | Psmd14 | Mm_Celera | 2:61756967 | TCAAAATGTTTTGAA[A/G]TCAAAATGGTCAAAC | 59029 |
rs28038974 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Psmd14 | Mm_Celera | 2:61756289 | GCCTGTCATATGTGT[C/T]CCTGCACCCTGATCA | 59029 |
rs28038975 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Psmd14 | Mm_Celera | 2:61755256 | TTGACAAAATTGGTC[C/T]GCAGATATACATATG | 59029 |
rs28038976 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Psmd14 | Mm_Celera | 2:61755125 | CATGGACTGATGACT[A/G]ATGAGCTTCCCCTTC | 59029 |
rs28038977 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Psmd14 | Mm_Celera | 2:61754723 | TTTCATCAGGACTCA[A/G]AGTTGCTGGAGAACC | 59029 |
rs28038978 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Psmd14 | Mm_Celera | 2:61754697 | GTAGTCTGAAATCAA[C/T]GATCTTGAAGTTTCA | 59029 |
rs28038979 | snp | C/G | 0.32 | 0.24 | intron-variant | Psmd14 | Mm_Celera | 2:61754677 | CATTGGCTTATAGTT[C/G]TAATGTAGTCTGAAA | 59029 |
rs28038980 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Psmd14 | Mm_Celera | 2:61753844 | CAGAATGCAGGGATT[C/G]TTGACTTAAATGTGT | 59029 |
rs28038981 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Psmd14 | Mm_Celera | 2:61753586 | ACTTGGGGAGAAGCA[C/G]TTTGTATTAGTTTGT | 59029 |
rs28038982 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Psmd14 | Mm_Celera | 2:61753517 | AAGCGGATCCCTTTT[C/T]CCATCACTGTCTGTC | 59029 |
rs28038983 | snp | C/T | 0.455 | 0.143091 | intron-variant | Psmd14 | Mm_Celera | 2:61753493 | CCATGAAGAGTTGGC[C/T]GACTGAAGAAGCGGA | 59029 |
rs28038984 | snp | A/G | 0.32 | 0.24 | intron-variant | Psmd14 | Mm_Celera | 2:61752560 | CTTTGTGCTGTTGTG[A/G]AGTGCATTGTTTTAC | 59029 |
rs28038985 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Psmd14 | Mm_Celera | 2:61752506 | AATGTTTGTAGACCT[G/T]TGTGGTCATTTCTGT | 59029 |
rs28038986 | snp | C/T | 0.32 | 0.24 | intron-variant | Psmd14 | Mm_Celera | 2:61750225 | GAGAAGTTCAGTAGG[C/T]TTAGGATGGCAGTGT | 59029 |
rs28038987 | snp | C/T | 0.32 | 0.24 | intron-variant | Psmd14 | Mm_Celera | 2:61749721 | TCCTGGTTCCCTATT[C/T]GAGTTATAAAAAACA | 59029 |
rs28038988 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Psmd14 | Mm_Celera | 2:61748440 | TTCTTTGAAAAAGCA[C/T]CCATTTGAACTGAAA | 59029 |
rs28038989 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Psmd14 | Mm_Celera | 2:61746196 | ACTTAACCTTCAACT[C/T]TTTTGATCTGTGATG | 59029 |
rs28038990 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Psmd14 | Mm_Celera | 2:61746126 | TATTCCTTTAAACAC[C/T]CCAGAGCCTGGCTCT | 59029 |
rs28038991 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Psmd14 | Mm_Celera | 2:61745045 | GGGAGTCCAACAATT[G/T]TATGTGGTCACGAGA | 59029 |
rs28038992 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Psmd14 | Mm_Celera | 2:61744936 | AGCTAATGGCGTGAT[C/T]ACTCTTTAAAAGTTT | 59029 |
rs28038993 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Psmd14 | Mm_Celera | 2:61744792 | TCTTCCTTTAGAAGC[C/T]ATTTCAGTGTGTCAG | 59029 |