SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6284127 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Ncf2 | Mm_Celera | 1:152817795 | GGACAACTTCTTCCC[A/G]CTATTACTAAAAAGG | 17970 |
rs13466541 | snp | C/T | 0.497778 | 0.0332592 | synonymous-codon | Ncf2 | Mm_Celera | 1:152831634 | TACCTCTCCAGAATC[C/T]GATATTCCACCACCT | 17970 |
rs31171944 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ncf2 | Mm_Celera | 1:152828107 | GCAAGCCATCTTCCT[C/T]CTCCAATAAAGGGGG | 17970 |
rs31171945 | snp | A/C | 0.5 | 0 | intron-variant | Ncf2 | Mm_Celera | 1:152828069 | agaaaaaagaaaaaa[A/C]CAAAATCCTTCTAAG | 17970 |
rs31171946 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ncf2 | Mm_Celera | 1:152827823 | TCACTCAGTAAACCC[A/G]AGAAGCAGAGCGGCC | 17970 |
rs31171947 | snp | C/T | 0.5 | 0 | intron-variant | Ncf2 | Mm_Celera | 1:152827757 | AGCTATCACAGTCTC[C/T]TTCCTGTGTGCGTTT | 17970 |
rs31171948 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Ncf2 | Mm_Celera | 1:152827663 | ATTGCTTCGAAGCCC[A/G]GGTCAGAGGTGAGAG | 17970 |
rs31171949 | snp | C/G/T | 0.48 | 0.0979796 | intron-variant | Ncf2 | GRCm38.p3 | 1:152827655 | GGGAGGTCATTGCTT[C/G/T]GAAGCCCAGGTCAGA | 17970 |
rs31171950 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Ncf2 | Mm_Celera | 1:152827577 | AGACCCAAATGATGC[C/G]ATTGTGCTGAGACCA | 17970 |
rs31171951 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ncf2 | Mm_Celera | 1:152827576 | TAGACCCAAATGATG[C/T]GATTGTGCTGAGACC | 17970 |
rs31171952 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ncf2 | Mm_Celera | 1:152827505 | ATACCCTCACTCTAC[A/G]TCTGACTTGACGGCA | 17970 |
rs31171953 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ncf2 | Mm_Celera | 1:152827504 | AATACCCTCACTCTA[C/T]GTCTGACTTGACGGC | 17970 |
rs31172484 | snp | G/T | 0.142012 | 0.225474 | utr-variant-5-prime, intron-variant | Ncf2 | Mm_Celera | 1:152807431 | ATGGACACTGAAGAT[G/T]CTCCATCCTGTCTCA | 17970 |
rs31172485 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ncf2 | Mm_Celera | 1:152807254 | CTAAATCTGTGTTTA[C/T]AGAGACTAGTGAACT | 17970 |
rs31172486 | snp | A/T | 0.497041 | 0.0383476 | intron-variant | Ncf2 | Mm_Celera | 1:152807212 | TAAATTAACTTTGAC[A/T]TTACCAGGGCAGTAA | 17970 |
rs31172487 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ncf2 | Mm_Celera | 1:152806879 | CCAGGCAAAGAAGTG[A/G]GATAGGAAGGCCTGC | 17970 |
rs31172488 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Ncf2 | Mm_Celera | 1:152806835 | ACATAGGAGACTGGA[C/T]GAATGAGCCTGGAAG | 17970 |
rs31172489 | snp | A/G | 0.42 | 0.183303 | intron-variant | Ncf2 | Mm_Celera | 1:152806796 | CGTAATGTAGAGTGC[A/G]GAGTGGACTGTCGCA | 17970 |
rs31172490 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Ncf2 | Mm_Celera | 1:152806777 | AAAGGGACAATACTC[C/T]CTCCGTAATGTAGAG | 17970 |
rs31172491 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Ncf2 | Mm_Celera | 1:152806354 | GCTTATAAAAAGCCT[A/T]GTTTGGCTACAAGTC | 17970 |
rs31172492 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Ncf2 | Mm_Celera | 1:152806257 | AAATCACTTGGAAGT[C/T]TAAATGTCAGGCTAG | 17970 |
rs31172493 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Ncf2 | Mm_Celera | 1:152806243 | CTGAGAAGCCAAGGA[A/G]ATCACTTGGAAGTTT | 17970 |
rs31172814 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ncf2 | Mm_Celera | 1:152827488 | TTAGGTCTGCATGCG[A/G]AATACCCTCACTCTA | 17970 |
rs31172815 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ncf2 | Mm_Celera | 1:152827311 | GTTTTTGGATCTGGA[A/G]CAGTATTCCAAATTA | 17970 |
rs31172816 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ncf2 | Mm_Celera | 1:152827291 | CACCCAGAAAAGAAG[G/T]CTTTGTTTTTGGATC | 17970 |
rs31172817 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ncf2 | Mm_Celera | 1:152827252 | GGCTTTTGGTTTCCC[A/G]AATTGTGCCCTTGCC | 17970 |
rs31172818 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ncf2 | Mm_Celera | 1:152827212 | AGCAGCTTCACTGGC[A/G]AGGGTCAGGCCCAGG | 17970 |
rs31172819 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ncf2 | Mm_Celera | 1:152827148 | ATACTGGGGAAGGGT[C/T]GAGTTGAGGTCAATA | 17970 |
rs31172820 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ncf2 | Mm_Celera | 1:152827121 | TTAATTGTAGACCAG[C/T]GCTTTTGGAAAATAC | 17970 |
rs31172821 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ncf2 | Mm_Celera | 1:152827098 | AATGTCACATATTGT[A/G]GCAAACATTAATTGT | 17970 |
rs31172822 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ncf2 | Mm_Celera | 1:152827054 | TCTTGTCTGGCCAGG[A/G]GATGCTGAGTTGATT | 17970 |
rs31172823 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152826292 | CCATTTGCTCCTGTA[C/T]AAGAGACTCCTTTGG | 17970 |
rs31173304 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Ncf2 | Mm_Celera | 1:152806145 | CTAGCTCTGAAGGCT[A/G]GGTTGGGTAAGTCTC | 17970 |
rs31173305 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Ncf2 | Mm_Celera | 1:152806070 | GGACTTGGGAAAGAA[A/G]ACGAGGTCATGGGCT | 17970 |
rs31173306 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Ncf2 | Mm_Celera | 1:152806009 | GACACAAGAGCATAT[A/G]TAACTGCATGGGTGG | 17970 |
rs31173307 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ncf2 | Mm_Celera | 1:152805870 | TTCAGCCTATATGGT[A/G]ACAGGGACTAGAGAA | 17970 |
rs31173308 | snp | C/T | 0.5 | 0 | intron-variant | Ncf2 | Mm_Celera | 1:152805855 | GTTAACTGATGGTAT[C/T]TCAGCCTATATGGTG | 17970 |
rs31173309 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Ncf2 | Mm_Celera | 1:152805726 | ACCTGCCAGTCCCAC[A/G]AGGAGTCTGGAAAGA | 17970 |
rs31173310 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ncf2 | Mm_Celera | 1:152805148 | GAGGGAGTGGCCCTT[A/G]CAGCTGGGACACAAG | 17970 |
rs31173311 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ncf2 | Mm_Celera | 1:152805064 | ACTGTGTGCTGTGTG[A/G]GTCATGGCGGCCAGT | 17970 |
rs31173312 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Ncf2 | Mm_Celera | 1:152805028 | CATCATTACGAGCTG[A/G]CCCACAGGCTGTCGG | 17970 |
rs31173313 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152804922 | AGAACTTGGGTTCTG[A/T]CATAAGGACGCTTGG | 17970 |
rs31173634 | snp | C/G | 0.497041 | 0.0383476 | intron-variant | Ncf2 | Mm_Celera | 1:152826153 | GACCACCTCATGGGA[C/G]CTTGCGCAGCCTCTG | 17970 |
rs31173635 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ncf2 | Mm_Celera | 1:152826116 | TCTCCCGTCCTCTGC[C/T]GGTGGTCCTAAGAGA | 17970 |
rs31173636 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ncf2 | Mm_Celera | 1:152826099 | CGGCCCTGTCAGCTC[C/T]GTCTCCCGTCCTCTG | 17970 |
rs31173637 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ncf2 | Mm_Celera | 1:152826010 | AAACTGATCACAGGG[A/G]TTCAGCCGCCTCTCA | 17970 |
rs31173638 | snp | C/T | 0.5 | 0 | intron-variant | Ncf2 | Mm_Celera | 1:152825866 | AGCAGCACGCTCACC[C/T]TCTTGTCTGTTTCAG | 17970 |
rs31173639 | snp | C/G | 0.497041 | 0.0383476 | intron-variant | Ncf2 | Mm_Celera | 1:152825859 | GCCTGGCAGCAGCAC[C/G]CTCACCTTCTTGTCT | 17970 |
rs31173640 | snp | A/G | 0.5 | 0 | intron-variant | Ncf2 | Mm_Celera | 1:152825674 | TGATGTTGTATGACT[A/G]CCAGCAGTTTTTCAT | 17970 |
rs31173641 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152824824 | TATTTGGCTTTGACA[A/G]TTTGGACATGTGAGT | 17970 |
rs31173642 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152824809 | ACCTTATCTGATCTG[C/T]ATTTGGCTTTGACAA | 17970 |
rs31173643 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Ncf2 | Mm_Celera | 1:152824629 | GAGTCGGGAGAGGGC[C/T]AGCAGGAGATGCCCT | 17970 |
rs31174184 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ncf2 | Mm_Celera | 1:152804856 | TGGGGCATTGTGGGA[A/G]ATGTGATATGACTGA | 17970 |
rs31174185 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Ncf2 | Mm_Celera | 1:152804790 | CCAACCCTACATCCC[C/T]GACTTGGATTGGGGA | 17970 |
rs31174186 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Ncf2 | Mm_Celera | 1:152804755 | ACCACGCTCGGCTGT[A/G]CATCAGTTTTACATT | 17970 |
rs31174187 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Ncf2 | Mm_Celera | 1:152802697 | GTCATGGGTCGATAA[G/T]GCTTCAGGAGTTACA | 17970 |
rs31174188 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ncf2 | Mm_Celera | 1:152802629 | ATCACATGGTTTTTA[A/C]AGCATTCTTACATTC | 17970 |
rs31174189 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Ncf2 | Mm_Celera | 1:152801737 | GCCAACCAAATAAAA[C/T]AGCAGTCATGATTTT | 17970 |
rs31174190 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152801720 | TGTGACTAGGGTAGT[A/C]TGCCAACCAAATAAA | 17970 |
rs31174191 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152801567 | AATTACCCATTCAGC[C/T]AATCATGAGAGTTTT | 17970 |
rs31174192 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ncf2 | Mm_Celera | 1:152801547 | TCTCAATTGTTTATT[C/T]GGTTAATTACCCATT | 17970 |
rs31174193 | snp | G/T | 0.497041 | 0.0383476 | intron-variant | Ncf2 | Mm_Celera | 1:152801029 | CTCAGAATGTTAGGT[G/T]CTAGGTTCTGTGGGA | 17970 |
rs31174494 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Ncf2 | Mm_Celera | 1:152824561 | GGTTTCTACTGGGAT[G/T]CTGAGTCTTGGGACA | 17970 |
rs31174495 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152824517 | TCTCTCCAGCTTCTT[C/T]CATAACCCTGACCAT | 17970 |
rs31174496 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152824147 | TGCTCACATGAGCTC[A/G]CCTAATAACGTCTGG | 17970 |
rs31174497 | snp | C/T | 0.5 | 0 | intron-variant | Ncf2 | Mm_Celera | 1:152823955 | TGGTTGGAAAGGACT[C/T]TTCTTTTGATATGTT | 17970 |
rs31174498 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ncf2 | Mm_Celera | 1:152822488 | GAGAGTGTTGGGTAA[A/G]TAATACCAATATAAG | 17970 |
rs31174499 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Ncf2 | Mm_Celera | 1:152821926 | CCTGAAGTCCTGGCT[A/G]TCCAGCACAGTGCCA | 17970 |
rs31174500 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152821878 | GGGGATGTGCAGCCT[A/C]TAAACACGGTGAAGA | 17970 |
rs31174501 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152821799 | AAGCCACACCCTAGC[A/G]AATGGAACAGTACAG | 17970 |
rs31174502 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Ncf2 | Mm_Celera | 1:152821479 | GGTGCCTGGTTTTGG[A/T]GCAGATTCAAGATTT | 17970 |
rs31174503 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152821168 | GCAAGAGCAGGAATT[C/T]GACATCACACACTCA | 17970 |
rs31175104 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ncf2 | Mm_Celera | 1:152800826 | CATATGCGATCCCAG[C/T]GCAATCATGAAAGAA | 17970 |
rs31175105 | snp | A/C | 0.459184 | 0.136902 | intron-variant | Ncf2 | Mm_Celera | 1:152800814 | CCGAAGAAACTGCAT[A/C]TGCGATCCCAGCGCA | 17970 |
rs31175106 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Ncf2 | Mm_Celera | 1:152800768 | AGCCTTAGATGTCCT[C/T]GGTGCGAGAGTCCTT | 17970 |
rs31175107 | snp | A/G | 0.197531 | 0.244432 | utr-variant-5-prime | Ncf2 | Mm_Celera | 1:152800325 | GTGTGTTTCTAACTC[A/G]TCACACTCTTCCTTT | 17970 |
rs31175108 | snp | C/T | 0.396694 | 0.202437 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799786 | ACCACATGCTTTCAG[C/T]TGCTACAACAGAGGA | 17970 |
rs31175109 | snp | C/G | 0.32 | 0.24 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799783 | ATGACCACATGCTTT[C/G]AGCTGCTACAACAGA | 17970 |
rs31175110 | snp | C/T | 0.473373 | 0.11227 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799777 | TGCAGAATGACCACA[C/T]GCTTTCAGCTGCTAC | 17970 |
rs31175111 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799748 | TCACTTACTGTCATA[C/T]GTTGGCAGACACATG | 17970 |
rs31175112 | snp | C/T | 0.489796 | 0.070696 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799691 | TGCTTTTGCTGTGGT[C/T]CAGACAACAGATCCC | 17970 |
rs31175113 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799663 | GGGAGTGTTTCGGTC[C/T]AAATGTGGGCCGTGC | 17970 |
rs31175364 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152820491 | TAATAAAGCAGACAC[C/T]GAGGAACCCACAATT | 17970 |
rs31175365 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Ncf2 | Mm_Celera | 1:152820446 | ATGTACAAAAGTGTA[A/G]TTGGTTCTTGTATGC | 17970 |
rs31175366 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152820352 | CTAGCATGGTAGAAT[C/T]GTTTGTTGGCAAGGA | 17970 |
rs31175367 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152818652 | TTTCTGTCACCTGTA[A/G]TAAATAGTAACGGGC | 17970 |
rs31175368 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ncf2 | Mm_Celera | 1:152818210 | TCCCTCCATAAGTTG[A/G]AGCAAACGCTTTGTT | 17970 |
rs31175369 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Ncf2 | Mm_Celera | 1:152818140 | CAAGGGAAGACTTGC[A/C]TTTGCTTTGGGAATT | 17970 |
rs31175370 | snp | A/G/T | 0.497041 | 0.0383476 | intron-variant | Ncf2 | GRCm38.p3 | 1:152818136 | CTCACAAGGGAAGAC[A/G/T]TGCATTTGCTTTGGG | 17970 |
rs31175371 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ncf2 | Mm_Celera | 1:152817675 | GAACCTGCTGTAACC[C/T]GCCTAGGTACTTGAT | 17970 |
rs31175372 | snp | A/T | 0.495868 | 0.0452663 | intron-variant | Ncf2 | Mm_Celera | 1:152817652 | ATCATGGGTTCTCTG[A/T]CTGTGAGGAACCTGC | 17970 |
rs31175373 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ncf2 | Mm_Celera | 1:152817293 | CCAGGATCTGACACC[A/G]GCATTGACAAAGGGA | 17970 |
rs31175872 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime, downstream-variant-500B | Smg7, Ncf2 | Mm_Celera | 1:152837455 | GGACTGGAGCAGCAC[A/G]GACAGTTTCTTTTGC | 17970 |
rs31175873 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime, downstream-variant-500B | Smg7, Ncf2 | Mm_Celera | 1:152837335 | GAATCAGTGACATTT[C/T]CAACCTCGGAATGCT | 17970 |
rs31175984 | snp | C/G/T | 0.497041 | 0.0383476 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799618 | GAACTTCACAGGCCT[C/G/T]GCTGTGTGTCCATTG | 17970 |
rs31175985 | snp | A/G | 0.497041 | 0.0383476 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799259 | AAATCCAAAACAAAA[A/G]GCAAGCTTGATGGCA | 17970 |
rs31175986 | snp | A/G | 0.48 | 0.0979796 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799176 | AGGTTTGGTCTCTCA[A/G]ATGGCCAGTCTGGCC | 17970 |
rs31175987 | snp | A/G | 0.408163 | 0.193609 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799096 | AAGTAGCCAGGAAGT[A/G]TCCTCTGGCCAAGGA | 17970 |
rs31175988 | snp | A/G | 0.18 | 0.24 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799080 | ATTAACTATTGATAG[A/G]AAGTAGCCAGGAAGT | 17970 |
rs31175989 | snp | G/T | 0.497041 | 0.0383476 | upstream-variant-2KB | Ncf2 | Mm_Celera | 1:152799059 | AAACAGTCAGACTAA[G/T]CTTTGATTAACTATT | 17970 |