SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3686905 | snp | C/T | 0.471655 | 0.115624 | intron-variant | Zfp106 | Mm_Celera | 2:120515719 | TGAGTTCATGGCCTA[C/T]GCAGGACAACTATGA | 20402 |
rs3687973 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Zfp106 | Mm_Celera | 2:120515854 | GCTCTTTACAGGATG[C/T]CTGTTCTAAGCCTCA | 20402 |
rs3687982 | snp | C/T | 0.483471 | 0.0893938 | intron-variant | Zfp106 | Mm_Celera | 2:120515856 | TCTTTACAGGATGCC[C/T]GTTCTAAGCCTCACC | 20402 |
rs3687997 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Zfp106 | Mm_Celera | 2:120515871 | TGTTCTAAGCCTCAC[C/G]GCACAGCAGCAGAAA | 20402 |
rs3689384 | snp | C/T | 0.5 | 0 | intron-variant | Zfp106 | Mm_Celera | 2:120516139 | ATTCCATAAAAGCAA[C/T]TTAAAAAAAAAAATT | 20402 |
rs3689387 | snp | A/C | 0.5 | 0 | intron-variant | Zfp106 | Mm_Celera | 2:120516143 | CATAAAAGCAATTTA[A/C]AAAAAAAAATTCAAA | 20402 |
rs3689904 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Zfp106 | GRCm38.p3 | 2:120516152 | AATTTAAAAAAAAAA[A/C/T]TTCAAAAACAGCTAA | 20402 |
rs6385147 | snp | G/T | 0.5 | 0 | intron-variant | Zfp106 | Mm_Celera | 2:120535962 | ACTTTTTTttttttt[G/T]gntttttcgagacaa | 20402 |
rs6385148 | snp | G/T | 0.5 | 0 | intron-variant | Zfp106 | Mm_Celera | 2:120535964 | TTTTTTtttttttng[G/T]tttttcgagacaagg | 20402 |
rs6385727 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Zfp106 | Mm_Celera | 2:120536086 | GATGGGATTAAAGGC[A/G]TGCTCCACCACCGCC | 20402 |
rs6385731 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Zfp106 | Mm_Celera | 2:120536090 | GGATTAAAGGCGTGC[A/T]CCACCACCGCCCAGG | 20402 |
rs6385777 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Zfp106 | Mm_Celera | 2:120536118 | AGGATTATTGTTAAT[A/G]TAACTCCATGTTCAG | 20402 |
rs6386814 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Zfp106 | Mm_Celera | 2:120536298 | GCCAAATAAGGGATC[C/T]CACAAGAAGCTAAAG | 20402 |
rs13462684 | snp | C/G | 0.444444 | 0.157135 | synonymous-codon | Zfp106 | Mm_Celera | 2:120522814 | AATATCTTCAGAGCC[C/G]GGAGATGATGAGGAG | 20402 |
rs13462685 | snp | A/G | 0.124444 | 0.216185 | missense | Zfp106 | GRCm38.p3 | 2:120520416 | ATCCGCTGCTACAAT[A/G]TTAAGGTGAGTGGCT | 20402 |
rs13462686 | snp | A/C | 0.444444 | 0.157135 | synonymous-codon | Zfp106 | GRCm38.p3 | 2:120519101 | AACCCTCTATGCTGG[A/C]CTAGCAAATGGCACT | 20402 |
rs13462687 | snp | A/C | 0.473373 | 0.11227 | missense | Zfp106 | GRCm38.p3 | 2:120523530 | ATCAAAGCATCTAAG[A/C]ACTCTTCAGGTAATT | 20402 |
rs13462688 | snp | A/G | 0.48 | 0.0979796 | utr-variant-3-prime | Zfp106 | GRCm38.p3 | 2:120509511 | GCTGCCCTGCGTACT[A/G]TATTTTAGAATTCAG | 20402 |
rs13462689 | snp | C/G | 0.475309 | 0.108333 | utr-variant-3-prime | Zfp106 | Mm_Celera | 2:120509194 | TGGGAGAAGCAGCTC[C/G]AGTCAGTTGATCGGC | 20402 |
rs27422268 | snp | A/C | 0.473373 | 0.11227 | intron-variant | Zfp106 | Mm_Celera | 2:120544142 | GCTCAGTTATTCAAG[A/C]TGGAACAAAGCGTTT | 20402 |
rs27422269 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Zfp106 | Mm_Celera | 2:120544129 | GAGTCAGCATGAGGC[C/T]CAGTTATTCAAGATG | 20402 |
rs27422270 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Zfp106 | Mm_Celera | 2:120543966 | TTTTAATGCAACTTA[C/T]TTGTTATGAGCTAGC | 20402 |
rs27422271 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Zfp106 | Mm_Celera | 2:120543421 | CTACAACAGCTGCTC[C/G]ATAAATAAAGGCATG | 20402 |
rs27422272 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Zfp106 | Mm_Celera | 2:120543334 | ACCACGCAATTTCCC[C/T]TCATGTACAAAAGGC | 20402 |
rs27422273 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Zfp106 | Mm_Celera | 2:120541088 | GAGGGCCATGGGATC[C/T]GACACCCATTTCTGA | 20402 |
rs27422274 | snp | C/G | 0.21875 | 0.248039 | intron-variant | Zfp106 | Mm_Celera | 2:120541076 | CAGAGAATTTCTGAG[C/G]GCCATGGGATCTGAC | 20402 |
rs27422275 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Zfp106 | Mm_Celera | 2:120540640 | TTCAAACTTAGTCTA[A/G]GTGCTTGTGCTATGG | 20402 |
rs27422276 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Zfp106 | Mm_Celera | 2:120540590 | TCTGTCTGTGCAACA[A/C]TAATGAGAAGCGTGC | 20402 |
rs27422277 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Zfp106 | Mm_Celera | 2:120540562 | AAGTTCTTTCAATCC[C/T]CTGATTACGTCATCT | 20402 |
rs27422278 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Zfp106 | Mm_Celera | 2:120540275 | TCAATAGCAAAATCT[C/T]CTCTTTGGCCAGTCT | 20402 |
rs27422279 | snp | C/G | 0.459184 | 0.136902 | intron-variant | Zfp106 | Mm_Celera | 2:120540111 | TAAAGGGAATTGAAA[C/G]CATGTCAAATGTAGG | 20402 |
rs27422280 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Zfp106 | Mm_Celera | 2:120539771 | ACTTAAAATCTTGCC[A/G]AAGGAAACATGGTGA | 20402 |
rs27422281 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Zfp106 | Mm_Celera | 2:120539622 | AGAGGGAATCAAGTC[A/G]GTGCTCCTCTCACCA | 20402 |
rs27422282 | snp | C/G | 0.46875 | 0.121031 | intron-variant | Zfp106 | Mm_Celera | 2:120539180 | TGTAGCTTAGGCTTA[C/G]TTAGTAGAGTGTACT | 20402 |
rs27422283 | snp | A/T | 0.5 | 0 | intron-variant | Zfp106 | Mm_Celera | 2:120538989 | ACCATAGTTTTCAGG[A/T]CTAAAAACAAGACTG | 20402 |
rs27422284 | snp | C/T | 0.375 | 0.216506 | intron-variant | Zfp106 | Mm_Celera | 2:120538381 | AACACTTGTGGACTT[C/T]ATTAATTGTTCTCTC | 20402 |
rs27422285 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Zfp106 | Mm_Celera | 2:120538344 | TAGAGTTGGAAGTTT[C/T]CTCATCACATAGAAG | 20402 |
rs27422286 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Zfp106 | Mm_Celera | 2:120538140 | AGTATCTGAAGGACC[A/G]CACAGCCCAAGGGGT | 20402 |
rs27422287 | snp | A/C/T | 0.486111 | 0.0821678 | intron-variant | Zfp106 | GRCm38.p3 | 2:120537860 | ATGTGAGTTGACTAT[A/C/T]TAAAGAGACCCTGCA | 20402 |
rs27422288 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Zfp106 | Mm_Celera | 2:120537222 | GTGCATGCCATAGTG[C/T]ATGTGTGCAATCAAG | 20402 |
rs27422289 | snp | A/G | 0.5 | 0 | intron-variant | Zfp106 | Mm_Celera | 2:120537218 | ACATGTGCATGCCAT[A/G]GTGTATGTGTGCAAT | 20402 |
rs27422290 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Zfp106 | Mm_Celera | 2:120536767 | CAACAGTTTCTGCAA[C/T]TGAATTTCTTTCTCT | 20402 |
rs27422291 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Zfp106 | Mm_Celera | 2:120536506 | ACCAGGTAATAAAGT[A/G]GCCTAAAATCTGCTT | 20402 |
rs27422292 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Zfp106 | Mm_Celera | 2:120535700 | AGAAAAAACAGTTTG[C/T]CATTATGGATTTAAT | 20402 |
rs27422293 | snp | A/G | 0.459184 | 0.136902 | missense, intron-variant | Zfp106 | Mm_Celera | 2:120535209 | TGAAATTTGTCTCCA[A/G]GGCCATTGTAATTCC | 20402 |
rs27422294 | snp | C/T | 0.391111 | 0.206368 | synonymous-codon, intron-variant | Zfp106 | Mm_Celera | 2:120534719 | TCCAGGAGGTCCTGC[C/T]TTTTGTGTTTTTATC | 20402 |
rs27422295 | snp | A/C | 0.444444 | 0.157135 | missense, intron-variant | Zfp106 | Mm_Celera | 2:120534417 | CGAGGACATAAACCG[A/C]GTGATTTGGATGTGT | 20402 |
rs27422296 | snp | C/T | 0.152778 | 0.230321 | synonymous-codon, intron-variant | Zfp106 | Mm_Celera | 2:120534305 | CAGTGTTTTGGGACA[C/T]TGTAGCACTGTGTCT | 20402 |
rs27422297 | snp | A/G | 0.444444 | 0.157135 | missense, intron-variant | Zfp106 | Mm_Celera | 2:120534258 | TTTGCATCGTTCTCC[A/G]TCCTTTTGGGTGTGG | 20402 |
rs27422298 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon, intron-variant | Zfp106 | Mm_Celera | 2:120533963 | TAAGCCAGAGTGTGG[A/G]CTGGTCGCTGCTGAC | 20402 |
rs27422299 | snp | C/T | 0.444444 | 0.157135 | missense, intron-variant | Zfp106 | Mm_Celera | 2:120533941 | GAGAGGTCTTCAAGT[C/T]TAGCAGTAAGCCAGA | 20402 |
rs27422300 | snp | G/T | 0.444444 | 0.157135 | synonymous-codon, intron-variant | Zfp106 | Mm_Celera | 2:120533587 | AGTTGACATTTCTCC[G/T]TGATGCATTTAGAAT | 20402 |
rs27422301 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Zfp106 | Mm_Celera | 2:120533362 | GTCATATAGGAACAG[C/T]CAGTGCTTAATACTG | 20402 |
rs27422302 | snp | C/T | 0.5 | 0 | intron-variant | Zfp106 | Mm_Celera | 2:120533340 | GTCAAGACAGACTAT[C/T]ACACGTGTCATATAG | 20402 |
rs27422303 | snp | A/T | 0.32 | 0.24 | intron-variant | Zfp106 | Mm_Celera | 2:120533297 | TCCAATTAGTGTTTC[A/T]GGTGCCTCCATTTTA | 20402 |
rs27422304 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Zfp106 | Mm_Celera | 2:120533294 | AGGTCCAATTAGTGT[C/T]TCAGGTGCCTCCATT | 20402 |
rs27422305 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Zfp106 | Mm_Celera | 2:120533003 | GCTCAGTGAAAGGTA[A/G]TAACAACAGGTAGTT | 20402 |
rs27422306 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Zfp106 | Mm_Celera | 2:120532323 | GCACAGAGGGAGGCT[C/G]CTGCTGTCAAGAAGC | 20402 |
rs27422307 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Zfp106 | Mm_Celera | 2:120532321 | CTGCACAGAGGGAGG[C/T]TCCTGCTGTCAAGAA | 20402 |
rs27422308 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Zfp106 | Mm_Celera | 2:120532291 | GCTGGGGAGTGTTAC[A/G]TGTGCTAGGCTCTCC | 20402 |
rs27422309 | snp | A/T | 0.487535 | 0.077957 | synonymous-codon | Zfp106 | Mm_Celera | 2:120531805 | GTGCAGGTCTCGGGC[A/T]GAATGCATGACAGGC | 20402 |
rs27422310 | snp | C/T | 0.493827 | 0.0552116 | synonymous-codon | Zfp106 | Mm_Celera | 2:120531766 | GGCATGGCGCTCTGA[C/T]AGTGGGGTAGACCTC | 20402 |
rs27422311 | snp | A/T | 0.49827 | 0.0293608 | missense | Zfp106 | Mm_Celera | 2:120531720 | AAGATGCATTTGATG[A/T]GAGTGAGTTTCCTTC | 20402 |
rs27422312 | snp | C/G | 0.188366 | 0.242283 | intron-variant | Zfp106 | Mm_Celera | 2:120531349 | ACTGCTGGGAGACCA[C/G]TTTTAGAGATGACTT | 20402 |
rs27422313 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Zfp106 | Mm_Celera | 2:120531245 | GCCAACATTTGCACA[C/T]GTCCTACAAACTCAG | 20402 |
rs27422314 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Zfp106 | Mm_Celera | 2:120531160 | CTGGGGAAGTGTTGC[A/G]GTGTTCATGTATACA | 20402 |
rs27422315 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Zfp106 | Mm_Celera | 2:120531069 | ATCATCATCATCACC[A/G]TTATTACCAGGGAGC | 20402 |
rs27422316 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Zfp106 | Mm_Celera | 2:120530940 | ACAGTACCTCCTCTG[C/T]CTGAAGGAGAACAGA | 20402 |
rs27422317 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Zfp106 | Mm_Celera | 2:120530894 | CTTCTCCAATTAAAT[C/T]CCAAGCTTCAAGTAT | 20402 |
rs27422318 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Zfp106 | Mm_Celera | 2:120530717 | GATGTACTAAAGCCC[A/G]CTGTGCCAAGCAATC | 20402 |
rs27422319 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Zfp106 | Mm_Celera | 2:120530641 | AGGCCTTGTGCACAA[C/T]GTAACCATTAGTTGA | 20402 |
rs27422320 | snp | A/T | 0.18 | 0.24 | intron-variant | Zfp106 | Mm_Celera | 2:120530634 | ACAACAGAGGCCTTG[A/T]GCACAACGTAACCAT | 20402 |
rs27422321 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Zfp106 | Mm_Celera | 2:120530583 | CAAAATGGTTGCCCT[A/G]TATGACCTTCTGCTA | 20402 |
rs27422322 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Zfp106 | Mm_Celera | 2:120530307 | CAGATTATCAAAAGG[A/C]TGAAGTGCTATCATG | 20402 |
rs27422323 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Zfp106 | Mm_Celera | 2:120529977 | CTATGTTTTAACCAG[A/G]TATGGTGTCATAAGT | 20402 |
rs27422324 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Zfp106 | Mm_Celera | 2:120529728 | AGCTGCAACTAGATG[A/G]AGCAAGCAGTCAATT | 20402 |
rs27422325 | snp | A/G | 0.5 | 0 | intron-variant | Zfp106 | Mm_Celera | 2:120529697 | TCAGTTCTATGTGGT[A/G]GCATGTATTTATCTT | 20402 |
rs27422326 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Zfp106 | Mm_Celera | 2:120529447 | CATTAGAAAAGCAAA[C/T]AAGGTGCCTCAAAAA | 20402 |
rs27422327 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Zfp106 | Mm_Celera | 2:120529358 | CCTGAGCAAAGTCTG[A/G]TTTTGATACTGAACA | 20402 |
rs27422328 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Zfp106 | Mm_Celera | 2:120529271 | GACGCTTCTCTTGGC[A/G]TGTGATGTAATCCCA | 20402 |
rs27422329 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Zfp106 | Mm_Celera | 2:120528897 | TTTGGCTGAGACTGA[A/G]CTTCAGGCTTACAGT | 20402 |
rs27422330 | snp | C/T | 0.18 | 0.24 | intron-variant | Zfp106 | Mm_Celera | 2:120528786 | CATTCAAAATAAGAA[C/T]CAGCAGGGATCTAAA | 20402 |
rs27422331 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Zfp106 | Mm_Celera | 2:120528758 | GGATCTTACTGACAT[C/G]AAAGCTCAAAAACAT | 20402 |
rs27422332 | snp | C/T | 0.473373 | 0.11227 | synonymous-codon | Zfp106 | Mm_Celera | 2:120528607 | TAAGGAAATAGTTAA[C/T]AGCTGGTCAACCTGA | 20402 |
rs27422333 | snp | A/G | 0.5 | 0 | intron-variant | Zfp106 | Mm_Celera | 2:120528126 | TCTCCCATCTCTCCC[A/G]TGTCAGCTTCCTAAG | 20402 |
rs27422334 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Zfp106 | Mm_Celera | 2:120527680 | CAAAAATGTCTAACA[A/G]GTACAAACTATCAAG | 20402 |
rs27422335 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Zfp106 | Mm_Celera | 2:120526963 | TGGATCCAGAAACCC[C/T]GGGAAAAAGGGTGCA | 20402 |
rs27422336 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Zfp106 | Mm_Celera | 2:120526450 | CTCCAACCCCACATT[C/T]TCTGAAGTACTTGAA | 20402 |
rs27422337 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Zfp106 | Mm_Celera | 2:120526095 | TTGGTTTACATATGA[C/G]GTAATAGATGCAGTA | 20402 |
rs27422338 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Zfp106 | Mm_Celera | 2:120525952 | TTGTAGTTATGAGAA[A/G]TTATCCTCAACTGTT | 20402 |
rs27422339 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Zfp106 | Mm_Celera | 2:120525130 | GGGCTTGCCTAACAC[A/G]CAATCTCCAGCAGCC | 20402 |
rs27422340 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Zfp106 | Mm_Celera | 2:120525074 | TATGGTTTAAGACAT[C/T]GAAATACAGCTCAGG | 20402 |
rs27422341 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Zfp106 | Mm_Celera | 2:120524620 | AGAGCCGTCATCGAC[C/T]ACTCCTGAATCAGGA | 20402 |
rs27422342 | snp | A/G | 0.124444 | 0.216185 | missense | Zfp106 | Mm_Celera | 2:120524192 | CTTGCAGGCTTAGCC[A/G]TGAACACATCCTGCT | 20402 |
rs27422344 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Zfp106 | Mm_Celera | 2:120523340 | GAAAAGGGAGCCACC[A/T]GAGCCTGACAGGAGT | 20402 |
rs27422345 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Zfp106 | Mm_Celera | 2:120522902 | CAACCTTATAGAGGA[C/T]CTGAAGTAAATCACT | 20402 |
rs27422347 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Zfp106 | Mm_Celera | 2:120522433 | TCACCTACTGGATGT[C/T]GGTTCAGAGAATAAA | 20402 |
rs27422348 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Zfp106 | Mm_Celera | 2:120522417 | GGGGCCTGACTGTTC[C/T]TCACCTACTGGATGT | 20402 |
rs27422349 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Zfp106 | Mm_Celera | 2:120522249 | TTCCAACAACCATTT[A/G]GTACAGCTACAGTGT | 20402 |
rs27422350 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Zfp106 | Mm_Celera | 2:120521902 | TTTTCACATCAATTC[C/T]AATCTTGAAAGTGTT | 20402 |