SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6327109 | snp | A/G | 0.5 | 0 | intron-variant | Bop1 | Mm_Celera | 15:76472827 | TTCTTGCTAGAGGCA[A/G]CACTAAGTCAGAACT | 12181 |
rs6327674 | snp | A/G | 0.5 | 0 | intron-variant | Bop1 | Mm_Celera | 15:76472962 | TTATGATACACAGAC[A/G]GACAGCACACCATAC | 12181 |
rs6328109 | snp | C/T | 0.5 | 0 | intron-variant | Bop1 | Mm_Celera | 15:76473009 | ATGTTTTAAAATTTG[C/T]tttattttatgtgta | 12181 |
rs6328180 | snp | C/T | 0.5 | 0 | intron-variant | Bop1 | Mm_Celera | 15:76473056 | tgtatgtctgtgcac[C/T]acatgcctgcttggt | 12181 |
rs6328716 | snp | C/T | 0.5 | 0 | intron-variant | Bop1 | Mm_Celera | 15:76473117 | ctaaaactggagtga[C/T]gggtggttgtgaact | 12181 |
rs6328748 | snp | C/G | 0.5 | 0 | intron-variant | Bop1 | Mm_Celera | 15:76473140 | tgtgaactaccatta[C/G]aggtacnggcaatca | 12181 |
rs6328765 | snp | C/T | 0.5 | 0 | intron-variant | Bop1 | Mm_Celera | 15:76473147 | taccattanaggtac[C/T]ggcaatcaaacccag | 12181 |
rs6328793 | snp | C/T | 0.5 | 0 | intron-variant | Bop1 | Mm_Celera | 15:76473164 | gcaatcaaacccagg[C/T]cctctggaagaacag | 12181 |
rs13464531 | snp | A/C | 0.260355 | 0.249785 | missense | Bop1 | Mm_Celera | 15:76474804 | GAAGGAGTGGCCGGA[A/C]CCAGCGGTGACGAAG | 12181 |
rs31775823 | snp | A/C/G | 0.375 | 0.216506 | intron-variant | Bop1 | GRCm38.p3 | 15:76473801 | GGAAGAAACAGGAAA[A/C/G]GGGGGGGCCGTGGGG | 12181 |
rs31966277 | snp | A/G | 0.49827 | 0.0293608 | missense | Bop1 | GRCm38.p3 | 15:76474848 | CTCGAGTCACTGCCC[A/G]AATCTTCGAGGCCTG | 12181 |
rs45733184 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Bop1 | Mm_Celera | 15:76474734 | GAGCCCATGGAAGCT[C/G]GTCCCTCACCCACCT | 12181 |
rs46433095 | snp | A/C | 0.244898 | 0.249948 | upstream-variant-2KB, intron-variant | Hsf1, Bop1 | Mm_Celera | 15:76477080 | TCCCTGGTCTTGCCA[A/C]GTGCCTGCATGGTTC | 12181 |
rs46475822 | snp | A/C/G | 0.231111 | 0.249285 | intron-variant | Bop1 | Mm_Celera | 15:76474097 | CCTACCATACCCAGA[A/C/G]GATCTAGGCCTGGCT | 12181 |
rs46703821 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Bop1 | Mm_Celera | 15:76474948 | CAGAGGGTTTAATAA[A/C]TGCCACCTGGAAGCA | 12181 |
rs46855309 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Bop1 | Mm_Celera | 15:76475356 | TCGGAAAGCTGAAGA[G/T]TAGCAAGATAAGCCT | 12181 |
rs46862467 | snp | A/C/G | | | intron-variant | Bop1 | Mm_Celera | 15:76473717 | AAAAGAAAAGAAAAA[A/C/G]AAAAAACAAAAAAAA | 12181 |
rs46911570 | snp | C/G | | | intron-variant | Bop1 | Mm_Celera | 15:76472611 | CTTCACAGTCTATGA[C/G]AGAAGACAAGTAGGG | 12181 |
rs47039143 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Bop1 | Mm_Celera | 15:76474515 | GTGGTCTGAGAATTG[C/T]CTGACGAGCAAAGAC | 12181 |
rs47240687 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, downstream-variant-500B | Bop1, Mroh1 | Mm_Celera | 15:76453306 | GGCCACATCCAGAAC[A/G]CCCAGATCTCGGGTC | 12181 |
rs47245876 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Bop1 | GRCm38.p3 | 15:76467017 | GACCACATGAAACAC[C/T]GTGCAACCCCAAATC | 12181 |
rs47247315 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Bop1 | Mm_Celera | 15:76475166 | GTGCCACCAAAACCA[A/G]GTTTCCTCCACGGAC | 12181 |
rs47307210 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Bop1 | Mm_Celera | 15:76468818 | CTCAGCAGCCTGGCT[A/G]CCTACGCGTCTCTCT | 12181 |
rs47500360 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Bop1 | Mm_Celera | 15:76472196 | CACACATGCAATAAT[A/G]ACAAATAAAACATAT | 12181 |
rs47528138 | snp | A/T | 0.142012 | 0.225474 | missense | Bop1 | Mm_Celera | 15:76474850 | CGAGTCACTGCCCAA[A/T]TCTTCGAGGCCTGAA | 12181 |
rs47841241 | snp | A/G | 0.336735 | 0.234472 | synonymous-codon | Bop1 | GRCm38.p3 | 15:76474856 | ACTGCCCAAATCTTC[A/G]AGGCCTGAAAACACA | 12181 |
rs47935467 | snp | A/C | | | intron-variant | Bop1 | Mm_Celera | 15:76472144 | CAAGATGTCCCCTGA[A/C]CACACACATATGCTG | 12181 |
rs48064213 | snp | A/G | 0.244898 | 0.249948 | upstream-variant-2KB, intron-variant | Hsf1, Bop1 | Mm_Celera | 15:76476971 | CCCTCGGCGCAAGTA[A/G]TGTTCTGCTGAGAGT | 12181 |
rs48179897 | snp | C/T | 0.391111 | 0.206368 | upstream-variant-2KB, intron-variant | Hsf1, Bop1 | Mm_Celera | 15:76476032 | GGCCTTCGCTGCCAA[C/T]CATCACAGTGATCAC | 12181 |
rs48319783 | snp | A/T | | | intron-variant | Bop1 | Mm_Celera | 15:76462907 | GGGACCACTCAGAAT[A/T]AAATGGTGTTCTCCC | 12181 |
rs48374117 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Bop1 | Mm_Celera | 15:76475313 | GCTTCTTTACCCTGA[A/C]GACCAGGACCAAGCC | 12181 |
rs48392831 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Bop1 | Mm_Celera | 15:76453762 | CCTGTAATTCTCACG[A/G]GATGCACAGGGTTCA | 12181 |
rs48452798 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Bop1 | Mm_Celera | 15:76469079 | TGCCACCCAATGAGA[A/G]TGCAAGTGACTGGTA | 12181 |
rs48494675 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Bop1 | Mm_Celera | 15:76472502 | ACAGAACAGGGACAC[A/G]TGATCCTTCTTTACC | 12181 |
rs48620985 | snp | G/T | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Hsf1, Bop1 | Mm_Celera | 15:76478442 | TGGCGGGTCTCTCGG[G/T]CTCTGCGGAGCACTG | 12181 |
rs48858860 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Bop1 | GRCm38.p3 | 15:76466799 | GCTGTCCTCTTCATA[C/T]TCATCTTGGGCCAGA | 12181 |
rs48936215 | snp | C/T | | | intron-variant | Bop1 | Mm_Celera | 15:76472622 | ATGACAGAAGACAAG[C/T]AGGGAGCAGGGAGGC | 12181 |
rs48987082 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Hsf1, Bop1 | Mm_Celera | 15:76478606 | AGAGAAGACTAGAAA[A/G]CACGGAACTTCACTT | 12181 |
rs49000376 | snp | A/G | 0.391111 | 0.206368 | upstream-variant-2KB, intron-variant | Hsf1, Bop1 | Mm_Celera | 15:76476882 | GAAGGTCCAGAGACT[A/G]TGGTGAGGGGACTCT | 12181 |
rs49328402 | snp | A/G | 0.142012 | 0.225474 | upstream-variant-2KB, intron-variant | Hsf1, Bop1 | Mm_Celera | 15:76476069 | TTCCATAGATGTCAC[A/G]CTGACATTCTCTTAT | 12181 |
rs49372677 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Bop1 | Mm_Celera | 15:76472005 | CGTTGGGCAGGGCGA[A/C]TGTAGACATTTTAAA | 12181 |
rs49430405 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Bop1 | GRCm38.p3 | 15:76467271 | CATCTGCGGGGCTAG[C/T]TACCCACACCACTCA | 12181 |
rs49556916 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon, downstream-variant-500B | Bop1, Mroh1 | GRCm38.p3 | 15:76453486 | CATGCCATGGCACAC[A/G]ATAACACTGCCGTCG | 12181 |
rs49833952 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, upstream-variant-2KB | Bop1, Scx | Mm_Celera | 15:76455697 | CTCATAGGGATTGAA[A/G]CCTGAATCTCCGAAC | 12181 |
rs49916618 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Bop1 | Mm_Celera | 15:76453761 | GCCTGTAATTCTCAC[A/G]AGATGCACAGGGTTC | 12181 |
rs49954187 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Bop1 | Mm_Celera | 15:76472763 | AAGATACTTCCTAGT[A/G]GCTAATCTCTGCTAT | 12181 |
rs50385336 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Bop1 | GRCm38.p3 | 15:76467328 | CAGCCGCAGTGACCC[A/T]GGGCCAATGGTCCCA | 12181 |
rs50392807 | snp | A/G | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | Hsf1, Bop1 | Mm_Celera | 15:76476143 | AAAAGTACTGCACGC[A/G]GTTAGGGCATAAACA | 12181 |
rs50457328 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Hsf1, Bop1 | Mm_Celera | 15:76478065 | CCTAAGGAATGCATG[A/G]GAGAAGAGCGAGAAT | 12181 |
rs50495195 | snp | A/T | | | intron-variant | Bop1 | Mm_Celera | 15:76472695 | CCAGACACCCACAGC[A/T]CCAAACTCCACACTC | 12181 |
rs50502796 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | Hsf1, Bop1 | Mm_Celera | 15:76476741 | AACCAGTTCTGGATG[C/T]CCTGGGTTCCAATCA | 12181 |
rs50561501 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Bop1 | GRCm38.p3 | 15:76467025 | GAAACACTGTGCAAC[C/T]CCAAATCTCTGAGCA | 12181 |
rs50656101 | snp | C/T | 0.244898 | 0.249948 | upstream-variant-2KB, utr-variant-5-prime | Hsf1, Bop1 | Mm_Celera | 15:76477245 | GCGCCGGCTACCGAT[C/T]TACTGCCGCTTCCGG | 12181 |
rs50681483 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Bop1, Scx | Mm_Celera | 15:76454790 | CACAGACACCGGAGG[A/G]CGTTTGCACCTCTGA | 12181 |
rs50703053 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Bop1 | GRCm38.p3 | 15:76467666 | CAGAGTGGGTGCCAC[C/G]GAGGATTCACACCGC | 12181 |
rs50843312 | snp | C/T | 0.5 | 0 | intron-variant | Bop1 | Mm_Celera | 15:76472535 | GCCTCACCTCTGACT[C/T]CCATGTGCGACTGTT | 12181 |
rs51028458 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Bop1 | GRCm38.p3 | 15:76467992 | CTATCTCCCCCACTT[C/T]CTTGCTGTACACCAA | 12181 |
rs51036038 | snp | A/G | | | intron-variant | Bop1 | Mm_Celera | 15:76472652 | CAGGGGAAGGGCGGG[A/G]CTCGGGAAGCTGAGA | 12181 |
rs51215924 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Bop1 | GRCm38.p3 | 15:76467679 | ACGGAGGATTCACAC[C/T]GCAACCTGGAAAACA | 12181 |
rs51240090 | snp | A/G | 0.132653 | 0.220748 | synonymous-codon | Bop1 | GRCm38.p3 | 15:76474799 | GTTGTCTTCGTCACC[A/G]CTGGATCCGGCCACT | 12181 |
rs51379649 | snp | A/G | 0.336735 | 0.234472 | missense | Bop1 | GRCm38.p3 | 15:76474755 | TCACCCACCTGTGCC[A/G]GCTCCTCAGAGGTCT | 12181 |
rs51419874 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Bop1 | Mm_Celera | 15:76474458 | GTCTCTAGAAAACTC[A/G]AGACGATCCCTAGAC | 12181 |
rs51431119 | snp | A/G | | | intron-variant | Bop1 | Mm_Celera | 15:76472118 | CACTGGAAGAATAGA[A/G]TCAATTCTCACAAGA | 12181 |
rs51549945 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | Hsf1, Bop1 | GRCm38.p3 | 15:76475796 | AGGCCACTTTACAAC[A/G]AACACAATAAGACAT | 12181 |
rs51586494 | snp | A/C | | | intron-variant | Bop1 | Mm_Celera | 15:76472137 | ATTCTCACAAGATGT[A/C]CCCTGACCACACACA | 12181 |
rs51707265 | snp | G/T | 0.444444 | 0.157135 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | Bop1, Mroh1 | Mm_Celera | 15:76452920 | TGCCTGAGGCTGACT[G/T]CACTCCTGCGAGTGA | 12181 |
rs51800475 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Bop1 | Mm_Celera | 15:76471936 | GGTTGACACAGCACA[C/T]GACACAAGGTCTAGC | 12181 |
rs51869232 | snp | A/T | | | intron-variant, utr-variant-3-prime | Bop1, Scx | Mm_Celera | 15:76458793 | TGGTGGCACCGGAAA[A/T]GCAGGGTGAGCAGGG | 12181 |
rs51870179 | snp | C/T | | | intron-variant | Bop1 | Mm_Celera | 15:76472123 | GAAGAATAGAGTCAA[C/T]TCTCACAAGATGTCC | 12181 |
rs51979777 | snp | A/T | | | intron-variant | Bop1 | Mm_Celera | 15:76471670 | GTTTCCAGCATCCAC[A/T]TGGCAGCTCACAACT | 12181 |
rs52396838 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Bop1 | Mm_Celera | 15:76469316 | TTAGGTGACAGAAGG[C/T]CCCTCAGAGGTCAGG | 12181 |
rs52585092 | snp | C/T | 0.5 | 0 | intron-variant | Bop1 | Mm_Celera | 15:76471831 | TACCAAGCTCACCAA[C/T]ACTGGGGTCTGGCTG | 12181 |
rs211784856 | in-del | -/G | | | intron-variant | Bop1 | Mm_Celera | 15:76475251 | TGGGACCCTGGGCCT[-/G]GGGGGGATTAGAACT | 12181 |
rs211789331 | in-del | -/AGAG | | | intron-variant | Bop1 | Mm_Celera | 15:76474021 | AGAAACCTACAAAAA[-/AGAG]AGAGAGAGAGAGAAT | 12181 |
rs211857098 | snp | C/T | | | intron-variant | Bop1, Scx | Mm_Celera | 15:76458554 | GTATATCTATACGCT[C/T]CCATCCAGAGGGGAA | 12181 |
rs211893453 | snp | A/G | | | intron-variant, upstream-variant-2KB | Bop1, Scx | Mm_Celera | 15:76455810 | TGCGCCTGAGGGAAA[A/G]CCAGTCAGGGCCATA | 12181 |
rs211984297 | snp | A/G | | | intron-variant | Bop1 | Mm_Celera | 15:76470331 | TACATACACGTATGT[A/G]CACATGCACATACAA | 12181 |
rs212009819 | snp | C/G | | | intron-variant, upstream-variant-2KB | Hsf1, Bop1 | Mm_Celera | 15:76477898 | CCCCAGAGCCACTCA[C/G]GGAGAGTAGGCCGAG | 12181 |
rs212053257 | snp | A/G | | | intron-variant | Bop1 | Mm_Celera | 15:76469479 | GGTGGGCAGCACAGT[A/G]TATACAACTTGAGGA | 12181 |
rs212053314 | snp | G/T | | | intron-variant, upstream-variant-2KB | Hsf1, Bop1 | Mm_Celera | 15:76479059 | TTAGCGTGCTGGGAG[G/T]CATGGGCAAGTAGTC | 12181 |
rs212190298 | snp | A/T | | | intron-variant | Bop1 | Mm_Celera | 15:76473569 | GAACCAGCTGGGCAG[A/T]GGTGCCGCACACCTT | 12181 |
rs212397603 | snp | C/G | | | intron-variant | Bop1 | Mm_Celera | 15:76461199 | GACAAGAGCCAGAGA[C/G]GCTTGGGTGTCAAGA | 12181 |
rs212401487 | in-del | -/A | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | Bop1, Scx | Mm_Celera | 15:76459170 | CACTAGTGAAGGTGG[-/A]ATGCCACTGAAGAGT | 12181 |
rs212787561 | snp | C/T | | | intron-variant | Bop1 | Mm_Celera | 15:76462984 | GCCGGGCACAGGCTT[C/T]ATCCGTAGCTTTTAT | 12181 |
rs212989797 | in-del | -/G | | | intron-variant | Bop1 | Mm_Celera | 15:76468348 | CATATACCTGGGGGA[-/G]GCCAAATGCTAGTAG | 12181 |
rs213122967 | snp | C/G | | | intron-variant | Bop1 | GRCm38.p3 | 15:76466027 | CGCTCAGCCCCGGGA[C/G]CAGGCCTCACCAGGG | 12181 |
rs213237177 | snp | A/C | | | intron-variant | Bop1 | Mm_Celera | 15:76474396 | CATCCTCCCTCGCAA[A/C]CACGTACCACTGGCA | 12181 |
rs213277079 | snp | A/T | | | intron-variant | Bop1 | GRCm38.p3 | 15:76464632 | AACACCGCACAGGCA[A/T]ATGACAACAGGGCTA | 12181 |
rs213297441 | snp | A/G | | | intron-variant | Bop1 | Mm_Celera | 15:76469295 | CAAACAAAAAAGAGC[A/G]GGGTATTAGGTGACA | 12181 |
rs213455890 | snp | C/T | | | intron-variant | Bop1 | Mm_Celera | 15:76468676 | GATTGTCTCAAACTA[C/T]CCTCCAGATTCAGCC | 12181 |
rs213499201 | in-del | -/G | | | intron-variant, upstream-variant-2KB | Bop1, Scx | GRCm38.p3 | 15:76455626 | CAAAGATGTTAGGTT[-/G]GGGGGGGCAGGGCGT | 12181 |
rs213500497 | in-del | -/TCAGAAG | | | intron-variant | Bop1 | Mm_Celera | 15:76470837 | CAAAAGAAGAGTAAC[-/TCAGAAG]TGCCTGAGGGAGGCT | 12181 |
rs213532942 | in-del | -/ACACACACACACACAC | | | intron-variant | Bop1 | Mm_Celera | 15:76471536 | ATCAATCTCCGGCAT[-/ACACACACACACACAC]ACACACACACACACA | 12181 |
rs213665425 | snp | G/T | | | upstream-variant-2KB, intron-variant | Hsf1, Bop1 | Mm_Celera | 15:76475664 | AGCTTCCAAGTAAGC[G/T]CTTCCTTTGATAAGG | 12181 |
rs213908736 | snp | C/T | | | upstream-variant-2KB, intron-variant | Hsf1, Bop1 | Mm_Celera | 15:76476322 | CATATCAAATAATTA[C/T]GATTCATAACAGTAG | 12181 |
rs213952660 | in-del | -/AG | | | intron-variant | Bop1 | Mm_Celera | 15:76474022 | AGAAACCTACAAAAA[-/AG]AGAGAGAGAGAATAG | 12181 |
rs214233677 | snp | C/G | | | intron-variant, utr-variant-3-prime | Bop1, Scx | Mm_Celera | 15:76458773 | TTTACTGCTCTGGCC[C/G]CACTTGGTGGCACCG | 12181 |
rs214330906 | snp | A/G | | | intron-variant, upstream-variant-2KB | Hsf1, Bop1 | Mm_Celera | 15:76479138 | GCTGGTATAAGAGAC[A/G]GTGGTCAGTGGGAGC | 12181 |
rs214357285 | snp | C/T | | | intron-variant | Bop1 | Mm_Celera | 15:76470454 | GCAAAGGCCCTAGGC[C/T]TAACAGCAGCAGGAT | 12181 |
rs214395348 | snp | A/G | | | intron-variant | Bop1 | Mm_Celera | 15:76471496 | TGCAAAAATAAATAC[A/G]GTAAATATACGTGAA | 12181 |