SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3657696 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Nphp1 | Mm_Celera | 2:127757672 | AAGGAATAGTGAGCT[C/G]ACTTACTTTGCTGGA | 53885 |
rs3661298 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Nphp1 | GRCm38.p3 | 2:127767689 | AGGAAAGGGGCTGGG[A/C/T]GCCAGAGCACCATGC | 53885 |
rs3661891 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nphp1 | Mm_Celera | 2:127767826 | CAGCTAAAGCACTTG[C/T]TATGTGAACTTCAGG | 53885 |
rs3661892 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nphp1 | Mm_Celera | 2:127767827 | AGCTAAAGCACTTGT[C/T]ATGTGAACTTCAGGA | 53885 |
rs3671689 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Nphp1 | Mm_Celera | 2:127770895 | GTCTATGTCAGATGG[A/G]ATTTAAATTAAAAAT | 53885 |
rs3683106 | snp | C/T | 0.5 | 0 | intron-variant | Nphp1 | Mm_Celera | 2:127784458 | TGACATGACTGCTTG[C/T]ATCCCTTGGTTGAGT | 53885 |
rs3683110 | snp | C/G | 0.5 | 0 | intron-variant | Nphp1 | Mm_Celera | 2:127784463 | TGACTGCTTGTATCC[C/G]TTGGTTGAGTGTGTG | 53885 |
rs3683160 | snp | C/T | 0.5 | 0 | intron-variant | Nphp1 | Mm_Celera | 2:127784482 | GTTGAGTGTGTGGAA[C/T]GAGAGTGTAGAAGGT | 53885 |
rs3687133 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Nphp1 | Mm_Celera | 2:127771093 | CAAATGTCTGAAGGG[A/T]AATAATCCTCATTAA | 53885 |
rs3687799 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Nphp1 | Mm_Celera | 2:127771219 | ACCTGGCTAACCTGT[C/T]ATTTAGTTCTGTTAT | 53885 |
rs6331578 | snp | A/C | 0.375 | 0.216506 | intron-variant | Nphp1 | Mm_Celera | 2:127756300 | GTCAGGATGCAGACT[A/C]TTCTATGAGGTAACA | 53885 |
rs6332652 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Nphp1 | Mm_Celera | 2:127756483 | GAAGTCAGTATTCAG[C/G]TGTGCCCCTCCCCTT | 53885 |
rs6332672 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Nphp1 | Mm_Celera | 2:127756491 | TATTCAGCTGTGCCC[A/C]TCCCCTTCCCTGCTA | 53885 |
rs28269097 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Nphp1 | Mm_Celera | 2:127776339 | CTACTCGGTCTTCGG[A/G]ATCATGTCCTAGGCA | 53885 |
rs28269098 | snp | C/T | 0.48 | 0.0979796 | synonymous-codon | Nphp1 | Mm_Celera | 2:127772152 | TTCAGCATCCTTAGC[C/T]AGCCACCAACCATCA | 53885 |
rs28269099 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Nphp1 | Mm_Celera | 2:127758226 | TCTCAGGATCAGAGT[A/C]CGCACACGGGGGATC | 53885 |
rs28269100 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Nphp1 | Mm_Celera | 2:127758108 | AGAGGAATCAGTAAC[G/T]CAAGGATCCCTTTCC | 53885 |
rs28269101 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nphp1 | Mm_Celera | 2:127758057 | CACAGGATCCTACAC[A/G]GCATTTTGAAGCTTT | 53885 |
rs28269102 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Nphp1 | Mm_Celera | 2:127756872 | TACAATGATAACTAA[C/T]GTCCTCTCCTCCTTG | 53885 |
rs28269103 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Nphp1 | Mm_Celera | 2:127756271 | CATCTTACTAAACTC[A/T]TGGGTAAATCAGAGT | 53885 |
rs28269104 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Nphp1 | Mm_Celera | 2:127756224 | CATTTATTTGTCAAC[G/T]AGACTCTGCCAGGAA | 53885 |
rs28269105 | snp | C/T | 0.32 | 0.24 | intron-variant | Nphp1 | Mm_Celera | 2:127755822 | GGACACATTCAGGCA[C/T]TCAGACACTGGGCTG | 53885 |
rs28269106 | snp | C/G | 0.396694 | 0.202437 | intron-variant | Nphp1 | Mm_Celera | 2:127755549 | GCCACTGCAAGGCCC[C/G]GGAGTGCTGCAGACA | 53885 |
rs28269107 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Nphp1 | Mm_Celera | 2:127755513 | TTCGTTTACGGAAAG[A/G]AGGGTAATAAGGTTC | 53885 |
rs28269108 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Nphp1 | Mm_Celera | 2:127755429 | CTGATGGCACGTGAA[A/G]GATTTGGCTCCAAGG | 53885 |
rs28269109 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Nphp1 | Mm_Celera | 2:127755416 | CTCAGCGTTCGCACT[A/G]ATGGCACGTGAAGGA | 53885 |
rs28269110 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Nphp1 | Mm_Celera | 2:127755403 | AATCACTTAGTGGCT[C/T]AGCGTTCGCACTGAT | 53885 |
rs28269111 | snp | G/T | 0.396694 | 0.202437 | intron-variant | Nphp1 | Mm_Celera | 2:127754924 | TCTCTATCTGTCAAG[G/T]ATTTTGCTGGCAGTT | 53885 |
rs28269112 | snp | A/C | 0.396694 | 0.202437 | intron-variant | Nphp1 | Mm_Celera | 2:127754870 | AACTTGGCATGCATT[A/C]AAAAATCTACATCCT | 53885 |
rs28269113 | snp | A/C | 0.396694 | 0.202437 | intron-variant | Nphp1 | Mm_Celera | 2:127754712 | GATAGTGGAGGAGAG[A/C]TGCATGTCTGCTGAC | 53885 |
rs28269114 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Nphp1 | Mm_Celera | 2:127754350 | TTAGACTCCATGTCT[A/G]TTCTCCAAAGCCAAA | 53885 |
rs28269115 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Nphp1 | Mm_Celera | 2:127754281 | TGACAGATGCTCTGC[A/G]GTATGAAGGGAGCTG | 53885 |
rs28269116 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Nphp1 | Mm_Celera | 2:127754199 | CAGTGGTCACCTGCC[C/T]AGCTTCTATGAGCCT | 53885 |
rs28269117 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Nphp1 | Mm_Celera | 2:127754145 | CAAACACACATTCAA[C/T]GAGAATCTACAGCCA | 53885 |
rs28269118 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Nphp1 | Mm_Celera | 2:127754122 | AAGTGCTTGGGACGG[C/T]GTTCATTCAAACACA | 53885 |
rs28269119 | snp | A/G | 0.165289 | 0.235211 | synonymous-codon, intron-variant | Nphp1 | Mm_Celera | 2:127754065 | CTGACGGAAAACACT[A/G]CCCTGTGCTACAAAA | 53885 |
rs28269120 | snp | A/G | 0.396694 | 0.202437 | synonymous-codon, intron-variant | Nphp1 | Mm_Celera | 2:127754041 | AGGCTGCCTGCGCAC[A/G]CTTATCATCTGACGG | 53885 |
rs28269121 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Nphp1 | Mm_Celera | 2:127753890 | GCTTTATCACTGCTG[C/T]GCTGCTCAGAGGCAA | 53885 |
rs28269122 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Nphp1 | Mm_Celera | 2:127753424 | CCCAGCACCATCCAT[A/G]AGGGTTTGGAAAATG | 53885 |
rs28269123 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Nphp1 | Mm_Celera | 2:127752953 | GGTAGATCTGAGATG[C/T]CACACATGTAGATTC | 53885 |
rs28269124 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Nphp1 | Mm_Celera | 2:127752596 | TCTGCAGCAGGCTCT[A/G]CCCTGTATGTCTTCC | 53885 |
rs28269125 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Nphp1 | Mm_Celera | 2:127752317 | TACCCCACACTTCAG[C/T]ATAACCTGGACTGAA | 53885 |
rs28269126 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Nphp1 | Mm_Celera | 2:127751895 | ACTAAGGACTTTTGC[C/T]ATGACCCTACAATAC | 53885 |
rs28269127 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Nphp1 | Mm_Celera | 2:127751264 | CTGGTTTCTCTGAGC[A/G]TCATCCTGTTTTTGG | 53885 |
rs28269128 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Nphp1 | Mm_Celera | 2:127751185 | CTGTGGAAAGCTCAC[A/G]TGCTGGTGCCCAGTC | 53885 |
rs28269129 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Nphp1 | Mm_Celera | 2:127751105 | TGGCTTGTCAGGGAC[A/G]TGAGGATGTTGAATA | 53885 |
rs28269130 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Nphp1 | Mm_Celera | 2:127750953 | GTATCATCTCTCACC[A/G]TCTAGCAGAAGAGAA | 53885 |
rs28269131 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Nphp1 | Mm_Celera | 2:127750921 | GAGCTTTGGCATAAC[A/G]GAAAGAGCTCCACAG | 53885 |
rs28269132 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Nphp1 | Mm_Celera | 2:127750893 | CGCCTGCAACCAGGC[C/T]TCCACTGTGTGTGAG | 53885 |
rs28269133 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Nphp1 | Mm_Celera | 2:127750769 | CACTTTGCACTTTCA[C/T]GTCTTCTGATATACA | 53885 |
rs28269134 | snp | C/G | 0.5 | 0 | intron-variant | Nphp1 | Mm_Celera | 2:127750064 | TGTAGAACTTACACA[C/G]ACCACTGCTCTAGGC | 53885 |
rs28269135 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Nphp1 | Mm_Celera | 2:127749501 | TGCCCTGATGCCACA[A/G]TGCCCTATGAGGTCA | 53885 |
rs28269136 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Nphp1 | Mm_Celera | 2:127748469 | CACCTGAAGAAAAGC[A/G]TGTGGCTGCCAAGCC | 53885 |
rs28269137 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Nphp1 | Mm_Celera | 2:127748374 | CTTGTGCTTCCATGC[A/G]AGCGCACACCCCCAT | 53885 |
rs28269138 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Nphp1 | Mm_Celera | 2:127748370 | CACGCTTGTGCTTCC[A/G]TGCGAGCGCACACCC | 53885 |
rs28269139 | snp | A/T | 0.165289 | 0.235211 | intron-variant | Nphp1 | Mm_Celera | 2:127748271 | CCACAACTTGGTCAC[A/T]TTAAACCAGAGATAA | 53885 |
rs28269140 | snp | A/G | 0.165289 | 0.235211 | synonymous-codon, missense | Nphp1 | Mm_Celera | 2:127748079 | CAGTAAGTGAGCAGA[A/G]CACATACTCCCCACC | 53885 |
rs28269141 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Nphp1 | Mm_Celera | 2:127747971 | CAAGGGTTTGCAGCA[C/T]TGACACACAGGAAAG | 53885 |
rs28269142 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Nphp1 | Mm_Celera | 2:127746988 | CACTTATTTTTAAAC[A/G]CTAGAGGGCTTCTTC | 53885 |
rs28269143 | snp | C/T | 0.5 | 0 | intron-variant | Nphp1 | Mm_Celera | 2:127746881 | CTCTTGCTCAGGTTT[C/T]ATCTTTGATTATCTA | 53885 |
rs28269144 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Nphp1 | Mm_Celera | 2:127746814 | GGTCTCCAGGCACAC[C/T]AGTTACTCTAATCAG | 53885 |
rs28269145 | snp | A/C | 0.5 | 0 | intron-variant | Nphp1 | Mm_Celera | 2:127746736 | TATCCTGATCCTCAA[A/C]TCTGTCCATGCCTGC | 53885 |
rs28269146 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Nphp1 | Mm_Celera | 2:127746569 | CAACTGATGGTGAAA[A/G]CTTAAGTACCACTCC | 53885 |
rs28269147 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Nphp1 | Mm_Celera | 2:127746246 | GAATTAGAAGGGTAG[C/T]TTGAATTCCTGGTAT | 53885 |
rs28269148 | snp | A/T | 0.165289 | 0.235211 | intron-variant | Nphp1 | Mm_Celera | 2:127746153 | CTCTGTGTCTCTACC[A/T]CTTATCCTAGAAAGT | 53885 |
rs28269149 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Nphp1 | Mm_Celera | 2:127745987 | GAAACACACAACAGG[A/G]AGATTCAAACTTCAT | 53885 |
rs28269150 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nphp1 | Mm_Celera | 2:127745835 | TGGGTTAGCTAGACA[A/G]TGAACAGGGACTGGG | 53885 |
rs28269151 | snp | A/G | 0.18 | 0.24 | intron-variant | Nphp1 | Mm_Celera | 2:127745769 | TCCCCTGCCACTGCA[A/G]CAGTGAAGGTTGCCC | 53885 |
rs28269152 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Nphp1 | Mm_Celera | 2:127745414 | CCAGAATGAATTTGG[C/T]CACAGCACACACCAT | 53885 |
rs28269153 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nphp1 | Mm_Celera | 2:127745382 | CATTTGATGCCATCA[C/T]TAAACCTTTGAGGTC | 53885 |
rs28269154 | snp | A/G | 0.18 | 0.24 | intron-variant | Nphp1 | Mm_Celera | 2:127745023 | GAGCCTATGCCTCCC[A/G]TCTCATGACTGTGGT | 53885 |
rs28269155 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nphp1 | Mm_Celera | 2:127744819 | TGTTCTAAAGGCTGT[A/G]TCAGGAGATGGGATT | 53885 |
rs28269156 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nphp1 | Mm_Celera | 2:127743964 | CTTCAGAGCCACAGC[A/G]TTTTACGACAGTCAG | 53885 |
rs28269157 | snp | A/G | 0.18 | 0.24 | intron-variant | Nphp1 | Mm_Celera | 2:127743852 | AGAATGTGATGGGCT[A/G]ACCATGAAGCGTTGG | 53885 |
rs28269158 | snp | A/T | 0.42 | 0.183303 | intron-variant | Nphp1 | Mm_Celera | 2:127743475 | CAGGAAGTCCAGCTA[A/T]GTCCCCTATACCAGC | 53885 |
rs28269159 | snp | A/G | 0.18 | 0.24 | intron-variant | Nphp1 | Mm_Celera | 2:127743294 | ACCCAGAACCAGCCT[A/G]ACAGGGATGGCAGGC | 53885 |
rs28269160 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Nphp1 | Mm_Celera | 2:127743240 | GTATAGCATCTAATG[C/T]GAAAGAGGTCACACT | 53885 |
rs28269161 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Nphp1 | Mm_Celera | 2:127743208 | TAGTTAAAGCTATGG[A/G]CAGGGTCGGGATAGC | 53885 |
rs28269162 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Nphp1 | Mm_Celera | 2:127743175 | AGTCCTGGCAACACC[A/T]TCTGCAGCTTCACCC | 53885 |
rs28269163 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Nphp1 | GRCm38.p3 | 2:127743016 | TCACTGAAACAGAGG[C/T]CTTGTTACAACACAT | 53885 |
rs28269164 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Nphp1 | Mm_Celera | 2:127742898 | GGTTGTTTAGGAGAC[C/T]TTAAGAAGCAAGCAT | 53885 |
rs28269165 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nphp1 | Mm_Celera | 2:127742616 | ACTTGCCAAGTTAGC[C/T]CATGTGTCTGCAGCA | 53885 |
rs28269166 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Nphp1 | Mm_Celera | 2:127742557 | AAGTGTCCATCAAGT[C/T]CTGCATTCTGGAAGT | 53885 |
rs28269167 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Nphp1 | Mm_Celera | 2:127742455 | CCTGCCATCTATGCC[A/G]CTTTTTCTTAATGAC | 53885 |
rs28283868 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Nphp1 | Mm_Celera | 2:127742453 | CACCTGCCATCTATG[C/T]CACTTTTTCTTAATG | 53885 |
rs28283869 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Nphp1 | Mm_Celera | 2:127742004 | CCCGCACCTCACCCA[C/T]TGTTGTTCTAGAAAG | 53885 |
rs28283870 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Nphp1 | Mm_Celera | 2:127741582 | GATAATTGCCTCAAT[C/T]TCAGAAAGAAGTGGG | 53885 |
rs28283871 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Nphp1 | Mm_Celera | 2:127741420 | TGAGAGCAAGGGTCT[C/T]CTAAGCTCCATGTAG | 53885 |
rs28283872 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Nphp1 | Mm_Celera | 2:127741327 | CATGTGCTCAGTGTT[A/G]TAAGAGCCCAGAGCT | 53885 |
rs28283873 | snp | A/G | 0.165289 | 0.235211 | synonymous-codon, utr-variant-3-prime | Nphp1 | Mm_Celera | 2:127741144 | AGGGAGCACGCAGTC[A/G]TGGTAGACCAGGAGG | 53885 |
rs28283874 | snp | C/T | 0.18 | 0.24 | synonymous-codon, utr-variant-3-prime | Nphp1 | Mm_Celera | 2:127740964 | GTCAAAGGTCTGCTC[C/T]GAAAGGTCAAATGGT | 53885 |
rs28283875 | snp | A/G | 0.493827 | 0.0552116 | downstream-variant-500B | Nphp1 | Mm_Celera | 2:127740306 | AAAAATCATTTTGAC[A/G]GAGGACTTTTTATAT | 53885 |
rs29498741 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nphp1 | Mm_Celera | 2:127775915 | TTATAGTGCTGATAT[A/G]TTTAGTGTTATACAG | 53885 |
rs29501740 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Nphp1 | Mm_Celera | 2:127778042 | GGTTTATGTAGTAAA[A/T]TTTTAGGCAGCCCAA | 53885 |
rs29502689 | snp | A/T | 0.375 | 0.216506 | intron-variant | Nphp1 | Mm_Celera | 2:127787408 | GTATTGCACTTTGCA[A/T]TCTTTTATATGTATA | 53885 |
rs29502805 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Nphp1 | GRCm38.p3 | 2:127790044 | CCCCACTTCTCTCTT[C/T]CCACTGTCATTTCTC | 53885 |
rs29504033 | snp | C/G | 0.375 | 0.216506 | intron-variant | Nphp1 | Mm_Celera | 2:127745859 | GACTGGGAAACACTG[C/G]CTGCAGCAGGTTTCC | 53885 |
rs29504700 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Nphp1 | Mm_Celera | 2:127744907 | AAGAACACTGGGCAC[A/T]TAACTTACTTCGTGC | 53885 |
rs29507198 | snp | G/T | 0.444444 | 0.157135 | upstream-variant-2KB | Nphp1 | Mm_Celera | 2:127789273 | TATTGTTAGTCTCAT[G/T]GTGTAGCCCTGAATT | 53885 |
rs29516030 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nphp1 | Mm_Celera | 2:127758629 | TCTCCATGCTGTGCC[C/T]ACTCATAAAAAAAAT | 53885 |