SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3698160 | snp | A/G | 0.5 | 0 | intron-variant | Usp25 | Mm_Celera | 16:77014463 | GACAGTTTCTCTTTC[A/G]GAGGTCTTATTGTGC | 30940 |
rs3713954 | snp | C/T | 0.5 | 0 | intron-variant | Usp25 | Mm_Celera | 16:77014787 | TTGTTTCTCGAACAG[C/T]ATCTTGCTAGTTCTA | 30940 |
rs4206930 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB | 1700041M19Rik, Usp25 | Mm_Celera | 16:77012001 | CAATTGACAGTGTGC[C/T]AAAAATCATTGAATG | 30940 |
rs4206931 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB | Usp25, 1700041M19Rik | Mm_Celera | 16:77012243 | TTAACTTTTTAAAAG[C/T]AGTGGTCCTGAAGAT | 30940 |
rs4206932 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Usp25 | Mm_Celera | 16:77013338 | GTTCTGGGCCCGCCC[A/G]GGTTTTGGGACATTA | 30940 |
rs4206933 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp25 | Mm_Celera | 16:77015535 | CATTTTCTTTATACT[C/T]ATTTTGCATTTTAAA | 30940 |
rs4206934 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp25 | Mm_Celera | 16:77016251 | CTGTCAGGGAAAGGA[A/G]GGGCTATCAGGAGCA | 30940 |
rs4206935 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp25 | Mm_Celera | 16:77018623 | TTTTTGTTTTATACA[C/T]ATATATATATATATA | 30940 |
rs4206936 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp25 | Mm_Celera | 16:77018652 | TATATACATATATAT[A/G]TGTGTGTGTATATAT | 30940 |
rs4206937 | snp | A/G | 0.5 | 0 | intron-variant | Usp25 | Mm_Celera | 16:77019464 | TGTTCTGATTTAGTT[A/G]GTGAAGAAGTTTTGG | 30940 |
rs4206938 | snp | C/G | 0.5 | 0 | intron-variant | Usp25 | GRCm38.p3 | 16:77020860 | TCTCTCTCTCTCTCT[C/G]TGTGTGTGTGTGTGT | 30940 |
rs4206939 | snp | C/G | 0.5 | 0 | intron-variant | Usp25 | GRCm38.p3 | 16:77020862 | TCTCTCTCTCTCTCT[C/G]TGTGTGTGTGTGTGT | 30940 |
rs4206944 | snp | A/G | 0.5 | 0 | intron-variant | Usp25 | Mm_Celera | 16:77024580 | TTGTGTTTCCCAGAG[A/G]CATTTGTTCTCTCAA | 30940 |
rs4206945 | snp | C/G | 0.375 | 0.216506 | intron-variant | Usp25 | Mm_Celera | 16:77028772 | TCTTCTGCTCACTTA[C/G]TTTCTGTCCCTGGCT | 30940 |
rs4206946 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp25 | Mm_Celera | 16:77028817 | TGCAGCCGACCTTCT[C/T]GTGCTGCCACCACAT | 30940 |
rs4206947 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp25 | Mm_Celera | 16:77028995 | AAGGTGTTCGCCCCA[C/T]TCAGGATGCTGTGCT | 30940 |
rs4206948 | snp | G/T | 0.5 | 0 | intron-variant | Usp25 | Mm_Celera | 16:77029199 | TCTGCAGCAGTGGCT[G/T]TATTGGTCACACTGC | 30940 |
rs4206949 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Usp25 | Mm_Celera | 16:77033591 | GCGTGGTGGCACTCA[C/G]CTCTAATCCCAGGTG | 30940 |
rs4206950 | snp | A/G | 0.5 | 0 | intron-variant | Usp25 | Mm_Celera | 16:77036792 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGCGC | 30940 |
rs4206951 | snp | G/T | 0.345679 | 0.230967 | intron-variant | Usp25 | Mm_Celera | 16:77046376 | GATCGAGTGCATACT[G/T]CTTAGTACATAGCTT | 30940 |
rs4206952 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp25 | Mm_Celera | 16:77055392 | TTCCTATCCCCTTTT[C/T]TGTATCATGAATGTG | 30940 |
rs4206953 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Usp25 | Mm_Celera | 16:77065679 | GATGGGAGCAGCTAT[A/C]TGAAGCTCCTGCCTT | 30940 |
rs4206954 | snp | G/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Usp25 | Mm_Celera | 16:77067162 | AGTAATAAGCATTCA[G/T]AATTAGTATAGCCAT | 30940 |
rs4206955 | snp | G/T | 0.401235 | 0.199068 | intron-variant | Usp25 | Mm_Celera | 16:77071357 | TGTCTGTGGCTAGGT[G/T]TGAAGGAATCCACAT | 30940 |
rs4206956 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp25 | Mm_Celera | 16:77072069 | ATGTTTTATGATTTC[C/T]CATTAAGGTAGTGGT | 30940 |
rs4206957 | snp | C/T | 0.42344 | 0.180051 | intron-variant | Usp25 | Mm_Celera | 16:77073177 | CTGTGAGCATCCTTT[C/T]GTGAGTTACAGAAAC | 30940 |
rs4206958 | snp | A/C | 0.396694 | 0.202437 | intron-variant | Usp25 | Mm_Celera | 16:77073192 | CGTGAGTTACAGAAA[A/C]TGTGCGGAAGACTCC | 30940 |
rs4206959 | snp | G/T | 0.362812 | 0.2231 | intron-variant | Usp25 | Mm_Celera | 16:77073950 | CAAGATTCCAGCCCA[G/T]CCCATTTTCCTCAGC | 30940 |
rs4206960 | snp | C/T | 0.42 | 0.183303 | intron-variant | Usp25 | Mm_Celera | 16:77075842 | GGCTGAGTGTGCCTA[C/T]GCTCTCACAAGTCAC | 30940 |
rs4206961 | snp | C/T | 0.42 | 0.183303 | synonymous-codon | Usp25 | Mm_Celera | 16:77076453 | TAAACCTGTGTGCAC[C/T]TCCCCCGTTGATGAC | 30940 |
rs4206962 | snp | C/T | 0.4608 | 0.1344 | intron-variant | Usp25 | Mm_Celera | 16:77077852 | TGGTGTGTGGGAGTG[C/T]GTGTGGATGAACACA | 30940 |
rs4206963 | snp | G/T | 0.4032 | 0.19756 | intron-variant | Usp25 | Mm_Celera | 16:77077910 | GAAAGACACTTTATT[G/T]TGAATTCATTTCTAA | 30940 |
rs4206964 | snp | C/T | 0.340265 | 0.233136 | intron-variant | Usp25 | Mm_Celera | 16:77078006 | ACATGTCAAAATATA[C/T]GTTACTAACTCTAAA | 30940 |
rs4206965 | snp | A/T | 0.340265 | 0.233136 | intron-variant | Usp25 | Mm_Celera | 16:77078067 | TTTTATATTAAAAGG[A/T]TGAGGTTACATTAAA | 30940 |
rs4206966 | snp | A/C | 0.4352 | 0.167931 | intron-variant | Usp25 | Mm_Celera | 16:77078608 | TAGATGAACCTGGGG[A/C]GCATTCATGCCTTAA | 30940 |
rs4206967 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp25 | Mm_Celera | 16:77083010 | CTCCTGCTCCCCCCT[C/T]TCCCATGCTCAACCA | 30940 |
rs4206968 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Usp25 | Mm_Celera | 16:77083195 | TTTAGCATTACAATA[A/C]ATAGCCACAGAGCAA | 30940 |
rs4206969 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp25 | Mm_Celera | 16:77083329 | TTAATCCCTTAACAT[A/G]AAAAACGGTTTTAGT | 30940 |
rs4206970 | snp | A/T | 0.375 | 0.216506 | intron-variant | Usp25 | Mm_Celera | 16:77083363 | ACTTTGAGCTTAACA[A/T]AGTCAGAGATTGCTT | 30940 |
rs4206971 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp25 | Mm_Celera | 16:77084331 | CCTTTTGACAGGAAG[C/T]TGTAATAACTGTGAT | 30940 |
rs4206972 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp25 | Mm_Celera | 16:77085361 | TGTCATGGTGCAGGA[C/T]GGTGTCTCAATGGCT | 30940 |
rs4206973 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp25 | Mm_Celera | 16:77085636 | TGACCCAAGTGATAG[A/G]ATCTAAGTGTGCAGG | 30940 |
rs4206974 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Usp25 | Mm_Celera | 16:77086146 | AGCTTTGCATCCTGT[G/T]TAAGAAGTGTGCATT | 30940 |
rs4206975 | snp | G/T | 0.375 | 0.216506 | intron-variant | Usp25 | Mm_Celera | 16:77088397 | TAACATCTTGGTGCA[G/T]AGTACACAGGGAGTA | 30940 |
rs4206976 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp25 | Mm_Celera | 16:77089330 | CAGGATCACTTCAAT[C/T]TGTTTTCACTGCGAT | 30940 |
rs4206977 | snp | C/G | 0.375 | 0.216506 | intron-variant | Usp25 | Mm_Celera | 16:77091364 | TTACACAATGGAGTA[C/G]TACTCAGCTATTAAA | 30940 |
rs4206978 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Usp25 | Mm_Celera | 16:77092973 | GCTGAAACCCAGTAA[C/G]GAAAAGCTTTGCTTG | 30940 |
rs4206979 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp25 | Mm_Celera | 16:77093543 | TTAGACATAAGCTCC[C/T]GGTTTCTGTATAGTG | 30940 |
rs4206980 | snp | C/T | 0.5 | 0 | intron-variant | Usp25 | Mm_Celera | 16:77093913 | TAAAACCCTCTCATA[C/T]GTTTCTTGTCAGAGG | 30940 |
rs4206981 | snp | A/G | 0.5 | 0 | intron-variant | Usp25 | Mm_Celera | 16:77094040 | GATGTGTCAATACTG[A/G]AGTAACTGAGAAAGT | 30940 |
rs4206982 | snp | C/T | 0.5 | 0 | intron-variant | Usp25 | Mm_Celera | 16:77094280 | CCCCACCCCCATTTT[C/T]GTAGTTAATACAAAC | 30940 |
rs4206983 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Usp25 | Mm_Celera | 16:77094492 | TAAACTACCCATTAA[C/G]CGAAGTTTCCAGCAA | 30940 |
rs4206984 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | Usp25 | Mm_Celera | 16:77096297 | ACAGTTCTTTTACAG[G/T]GTCCCTGTAGCTATT | 30940 |
rs4206985 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp25 | Mm_Celera | 16:77096497 | ATTGAGCTCAGTTTC[A/G]CTGCAAGAGCAGGAT | 30940 |
rs4206986 | snp | A/G | 0.5 | 0 | intron-variant | Usp25 | Mm_Celera | 16:77097820 | TGCAGATATGTACAA[A/G]CACCGTAGGCATGAC | 30940 |
rs4206987 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp25 | Mm_Celera | 16:77098850 | GACCACAGACTCTTA[A/G]CTGCACTGAGACAGC | 30940 |
rs4206988 | snp | A/G | 0.5 | 0 | intron-variant | Usp25 | Mm_Celera | 16:77098869 | CACTGAGACAGCGTC[A/G]TGCTACTTATTTCTA | 30940 |
rs4206989 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Usp25 | Mm_Celera | 16:77099091 | TTGTGACTACTCTCT[C/T]TATTGAATATACTAC | 30940 |
rs4206990 | snp | C/G | 0.5 | 0 | intron-variant | Usp25 | Mm_Celera | 16:77100005 | AGACATTAAGGGTAC[C/G]GGAAAACAATGACAT | 30940 |
rs4206991 | snp | C/G | 0.375 | 0.216506 | intron-variant | Usp25 | Mm_Celera | 16:77101975 | GATTAAGTACTTTCA[C/G]CTCTACTTATTAATG | 30940 |
rs4206992 | snp | C/T | 0.5 | 0 | intron-variant | Usp25 | Mm_Celera | 16:77101993 | CTACTTATTAATGCG[C/T]TATCATCAGACCAAT | 30940 |
rs4206993 | snp | A/T | 0.375 | 0.216506 | intron-variant | Usp25 | Mm_Celera | 16:77102310 | AAATAGGCTTGAGTA[A/T]GTGAACTGGTATGAT | 30940 |
rs4206994 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Usp25 | Mm_Celera | 16:77102442 | TTCTACCAAATCCTT[C/T]CCCAAGCTGTCTTCT | 30940 |
rs4206995 | snp | G/T | 0.32 | 0.24 | intron-variant | Usp25 | Mm_Celera | 16:77102564 | GACCATCTAGAGACT[G/T]CCATACCCGGGGATA | 30940 |
rs4206996 | snp | C/G | 0.32 | 0.24 | intron-variant | Usp25 | Mm_Celera | 16:77102636 | ACTAGCAAGATTTTG[C/G]TATAAGGACCCAGAT | 30940 |
rs4206997 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Usp25 | Mm_Celera | 16:77102674 | TCTCTTGTGAGACTA[C/T]GCCGGGGCCTAGCAA | 30940 |
rs4206998 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Usp25 | Mm_Celera | 16:77102677 | CTTGTGAGACTATGC[C/T]GGGGCCTAGCAAACA | 30940 |
rs4206999 | snp | G/T | 0.5 | 0 | intron-variant | Usp25 | Mm_Celera | 16:77103279 | AACATAGTGAATGAA[G/T]TCTAGTGAAAGATCT | 30940 |
rs4207000 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp25 | Mm_Celera | 16:77103431 | ATGCTGCATGGAAAT[A/G]CACTCACAAACATAC | 30940 |
rs4207001 | snp | A/C | 0.5 | 0 | intron-variant | Usp25 | Mm_Celera | 16:77103464 | ATGCACATACAAACA[A/C]ACAAACAAAAAAGAA | 30940 |
rs4207002 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Usp25 | Mm_Celera | 16:77103794 | CTTCTGTATTATGAA[A/G]TAAGGTTCTTGATAG | 30940 |
rs4207003 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Usp25 | Mm_Celera | 16:77104618 | ATGGGGGTAGGATAG[G/T]AGGATTTTTGGAGGG | 30940 |
rs4207004 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp25 | Mm_Celera | 16:77105500 | CTAGGATTGTACGTG[C/T]TTCTGTATTCTACTC | 30940 |
rs4207005 | snp | A/C | 0.5 | 0 | intron-variant | Usp25 | Mm_Celera | 16:77105651 | TTTATGATTTTTTAG[A/C]ATTAATTGTTACTTC | 30940 |
rs4207006 | snp | A/G | 0.5 | 0 | intron-variant | Usp25 | Mm_Celera | 16:77106521 | ATTAGGAGACTCACT[A/G]AGTAAATCCAGGAGA | 30940 |
rs4207007 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Usp25 | Mm_Celera | 16:77107128 | ATAAAGGGAAAATTT[A/G]AATGTGTTATTTTTA | 30940 |
rs4207008 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Usp25 | Mm_Celera | 16:77107158 | AATCATGTGGGCTTC[A/G]TGGGATTAATTCATC | 30940 |
rs4207009 | snp | A/G | 0.478299 | 0.101881 | synonymous-codon | Usp25 | Mm_Celera | 16:77107995 | TATCCAGAACCAGGC[A/G]CCAAAGAAAATCATT | 30940 |
rs4207010 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Usp25 | Mm_Celera | 16:77108631 | CTTGTTAGTCTGAAT[A/T]TCATTTAAAAAAGAC | 30940 |
rs4207011 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Usp25 | Mm_Celera | 16:77108633 | TGTTAGTCTGAATAT[C/T]ATTTAAAAAAGACTC | 30940 |
rs4207012 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Usp25 | Mm_Celera | 16:77108638 | GTCTGAATATCATTT[A/T]AAAAAGACTCCAAGT | 30940 |
rs4207013 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Usp25 | Mm_Celera | 16:77108675 | TTTCAAGATACTAAA[C/T]GTTACTTTTTTTTTT | 30940 |
rs4207014 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Usp25 | Mm_Celera | 16:77108750 | GTATAGACCAGGATA[C/G]ACTCAAACTCACAGA | 30940 |
rs4207015 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Usp25 | Mm_Celera | 16:77108904 | TGCTTGACATGGTAT[A/T]TGTGTGAAGTTATTT | 30940 |
rs4207016 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Usp25 | Mm_Celera | 16:77108980 | GGTATATGTGTGAAG[A/G]TCAGAGGACCACTCT | 30940 |
rs4207017 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Usp25 | Mm_Celera | 16:77109777 | GGTCTGTACATGAAC[A/T]CAGGAGGTATAGGGA | 30940 |
rs4207018 | snp | A/T | 0.375 | 0.216506 | intron-variant | Usp25 | Mm_Celera | 16:77110437 | TGGTGGAACTATCTC[A/T]AGATAAACCTTATAT | 30940 |
rs4207019 | snp | A/G | 0.5 | 0 | intron-variant | Usp25 | Mm_Celera | 16:77110456 | TAAACCTTATATTGA[A/G]TTTTTTATTTTTTAA | 30940 |
rs4207020 | snp | A/G | 0.5 | 0 | intron-variant | Usp25 | Mm_Celera | 16:77110599 | CACCGTAGGTCAGCA[A/G]AGTGCTTGGCAACAC | 30940 |
rs4207021 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Usp25 | Mm_Celera | 16:77112631 | TACTGGCCACATTCT[G/T]TGATCCATTTATGAC | 30940 |
rs4207022 | snp | C/T | 0.5 | 0 | intron-variant | Usp25 | Mm_Celera | 16:77113943 | GACTGTAAACACTGT[C/T]GGATAAAAATCATGA | 30940 |
rs4207023 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp25 | Mm_Celera | 16:77114297 | GTTACTTTAAAAATG[C/T]TTTTAGTCTACATTA | 30940 |
rs4207024 | snp | C/G/T | 0.375 | 0.216506 | intron-variant | Usp25 | GRCm38.p3 | 16:77114390 | GGAATTACAAATTCC[C/G/T]CCAAAATGTATTTGA | 30940 |
rs4207025 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Usp25 | Mm_Celera | 16:77115000 | CTTGTTGCTGGTGGA[C/T]GACATGGAAGAGAAA | 30940 |
rs4207026 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp25 | Mm_Celera | 16:77115255 | CATGTATGTAAAAAT[C/T]AACAAAAGCCAAACT | 30940 |
rs4207027 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp25 | Mm_Celera | 16:77115268 | ATCAACAAAAGCCAA[A/G]CTCAGATCCCCAAAT | 30940 |
rs4207028 | snp | C/G | 0.444444 | 0.157135 | synonymous-codon | Usp25 | Mm_Celera | 16:77115409 | CCTCCAAGAAAAGCT[C/G]ACGGATTTTCTGCCA | 30940 |
rs6180869 | snp | C/T | 0.5 | 0 | intron-variant | Usp25 | Mm_Celera | 16:77099223 | CAGATACACTGGTTG[C/T]ACAGTTGTACGAAGG | 30940 |
rs6181380 | snp | A/T | 0.5 | 0 | intron-variant | Usp25 | Mm_Celera | 16:77099294 | TCAGGCTATTCATTT[A/T]TTTACTAAGTGTTGG | 30940 |
rs6181943 | snp | A/C | 0.5 | 0 | intron-variant | Usp25 | Mm_Celera | 16:77099390 | TTCTTACAATTCTGC[A/C]CTTTAGAGAGAATGC | 30940 |