SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3657975 | snp | A/G | 0.5 | 0 | intron-variant | Zbtb7c | Mm_Celera | 18:75968794 | TGTGGCAATCCACTG[A/G]AGACCCGACCTTCCA | 207259 |
rs3668316 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Zbtb7c | GRCm38.p3 | 18:75875150 | GACTGTCACTGAGGG[C/T]GAGAGTCACCCCGCT | 207259 |
rs3676583 | snp | A/G | 0.5 | 0 | intron-variant | Zbtb7c | Mm_Celera | 18:75869912 | CCAGATTTGGGGCAT[A/G]CAAGACTGAAAGAAG | 207259 |
rs3676720 | snp | A/C | 0.5 | 0 | intron-variant | Zbtb7c | Mm_Celera | 18:75869985 | CTGGCTCCCCCTTTT[A/C]ATTAAACTTAGAGTC | 207259 |
rs3681356 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Zbtb7c | Mm_Celera | 18:76109521 | TGGAAGGGAGAGATA[C/T]TGAGGGGGGAATCCA | 207259 |
rs3682561 | snp | C/T | 0.375 | 0.216506 | intron-variant | Zbtb7c | Mm_Celera | 18:76109685 | TTTCTTCTTCTCACA[C/T]CCTTGTTGCCTTCTT | 207259 |
rs3690119 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Zbtb7c | GRCm38.p3 | 18:75833606 | TCCCACATCTAGTGA[C/T]CAGGCTTGAGATGTG | 207259 |
rs3691373 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Zbtb7c | GRCm38.p3 | 18:75833823 | GAAAGATTAGTGGGT[A/G]GAAGACCTGGATCTC | 207259 |
rs3693730 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Zbtb7c | Mm_Celera | 18:75933698 | CACAGCAAGTTTCCT[A/G]GGGACCCTACAACAT | 207259 |
rs3711268 | snp | A/G | 0.5 | 0 | intron-variant | Zbtb7c | GRCm38.p3 | 18:76113497 | CCTTTGGCTATATCT[A/G]AGCATGGTAGAGCTG | 207259 |
rs3711839 | snp | A/G | 0.5 | 0 | intron-variant | Zbtb7c | GRCm38.p3 | 18:76113566 | GCCACACTGATTTCC[A/G]CAGTGGCTGCACCAG | 207259 |
rs3711860 | snp | C/T | 0.5 | 0 | intron-variant | Zbtb7c | GRCm38.p3 | 18:76113576 | TTTCCACAGTGGCTG[C/T]ACCAGTGTGCACTCC | 207259 |
rs3711940 | snp | A/C | 0.5 | 0 | intron-variant | Zbtb7c | GRCm38.p3 | 18:76113610 | CAACGATGAAGGTTT[A/C]CCCTTTCCCTATATC | 207259 |
rs3711970 | snp | C/T | 0.5 | 0 | intron-variant | Zbtb7c | GRCm38.p3 | 18:76113627 | CCTTTCCCTATATCC[C/T]GGCCAGCATGTGCTG | 207259 |
rs3711986 | snp | C/T | 0.5 | 0 | intron-variant | Zbtb7c | GRCm38.p3 | 18:76113638 | ATCCTGGCCAGCATG[C/T]GCTGTCCTTTGTTTT | 207259 |
rs3715106 | snp | C/T | 0.5 | 0 | intron-variant | Zbtb7c | Mm_Celera | 18:76019454 | GTTTACACACGCACA[C/T]ACTTGGGTGTCTGAG | 207259 |
rs3715675 | snp | A/G | 0.5 | 0 | intron-variant | Zbtb7c | Mm_Celera | 18:76019504 | ATGGGAGGATATGGT[A/G]GACACGCCGTGGTCC | 207259 |
rs3715693 | snp | C/T | 0.5 | 0 | intron-variant | Zbtb7c | Mm_Celera | 18:76019512 | ATATGGTGGACACGC[C/T]GTGGTCCTTCATATC | 207259 |
rs3724679 | snp | A/T | 0.5 | 0 | intron-variant, nc-transcript-variant | Zbtb7c, 1700003O11Rik | Mm_Celera | 18:76015840 | CTTTTGATGGCTTTC[A/T]TTGTACCAGCTCTGT | 207259 |
rs6177568 | snp | C/G | 0.49827 | 0.0293608 | intron-variant | Zbtb7c | GRCm38.p3 | 18:75846847 | TTCAGGTGGAGACTC[C/G]TCATCTCAGCCATGG | 207259 |
rs6178087 | snp | A/T | 0.459184 | 0.136902 | intron-variant | Zbtb7c | GRCm38.p3 | 18:75846947 | CGTGCTAAACTCTTA[A/T]GCCCCTTTCTCCTCA | 207259 |
rs6178523 | snp | C/T | 0.5 | 0 | intron-variant | Zbtb7c | Mm_Celera | 18:75847011 | ACCACCGCCGCGCCT[C/T]CAACGCCACCNCCAA | 207259 |
rs6178544 | snp | A/G | 0.5 | 0 | intron-variant | Zbtb7c | Mm_Celera | 18:75847022 | GCCTNCAACGCCACC[A/G]CCAACATACACTCCA | 207259 |
rs6192528 | snp | C/T | 0.5 | 0 | intron-variant | Zbtb7c | Mm_Celera | 18:75847268 | CTAAGATGATGTCAT[C/T]TTTAGAGTCCAGTTT | 207259 |
rs6244133 | snp | C/T | 0.5 | 0 | intron-variant | Zbtb7c | GRCm38.p3 | 18:75856509 | TTTGGATGTCCCTCC[C/T]GGTTNTGAGGATCTT | 207259 |
rs6244147 | snp | C/T | 0.5 | 0 | intron-variant | Zbtb7c | GRCm38.p3 | 18:75856514 | ATGTCCCTCCNGGTT[C/T]TGAGGATCTTCCTTA | 207259 |
rs6244611 | snp | A/G | 0.5 | 0 | intron-variant | Zbtb7c | GRCm38.p3 | 18:75856557 | GTGAGGGCTCACCCC[A/G]GCGCTTCTGGGTGAA | 207259 |
rs6245859 | snp | C/T | 0.5 | 0 | intron-variant | Zbtb7c | GRCm38.p3 | 18:75856809 | aatgcagttagattt[C/T]taaaaaccataattc | 207259 |
rs6336967 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Zbtb7c | Mm_Celera | 18:76130245 | TTGGGTGCCTCTAAG[G/T]ACAAGCTGTCTGAGG | 207259 |
rs6337472 | snp | A/G | 0.5 | 0 | intron-variant | Zbtb7c | Mm_Celera | 18:76130269 | TCTGAGGACCCACAG[A/G]ATCCAGGTTAAACAC | 207259 |
rs6338029 | snp | A/C | 0.5 | 0 | intron-variant | Zbtb7c | Mm_Celera | 18:76130372 | AAACCCCCCTCTATT[A/C]CCCACTGCTCAGATA | 207259 |
rs6338177 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Zbtb7c | Mm_Celera | 18:76130453 | CCTTTCTGTCCACAC[C/T]TCTCCTTTCACAGGG | 207259 |
rs6355930 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Zbtb7c | GRCm38.p3 | 18:76032548 | TCCTCAAGTGGCCAG[A/G]CCAGTTAAGGNAAGG | 207259 |
rs6355946 | snp | A/C | 0.5 | 0 | intron-variant | Zbtb7c | GRCm38.p3 | 18:76032559 | CCAGNCCAGTTAAGG[A/C]AAGGTAGAACTGTGG | 207259 |
rs6373043 | snp | C/T | 0.499808 | 0.00980204 | intron-variant | Zbtb7c | Mm_Celera | 18:75995901 | AGGCTCTGGAGACCC[C/T]GTGCCTCTGAGACCT | 207259 |
rs6381624 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Zbtb7c | Mm_Celera | 18:75950905 | CACAAGGAGCTGTTA[C/T]GAATATTCTCTGTGG | 207259 |
rs6396758 | snp | G/T | 0.487535 | 0.077957 | intron-variant | Zbtb7c | Mm_Celera | 18:75951317 | AACAAGCATCTCCAC[G/T]TTGGCCAGTGTTGTC | 207259 |
rs6397954 | snp | A/G | 0.5 | 0 | intron-variant | Zbtb7c | Mm_Celera | 18:75924635 | ATGTGGCTCTGAGAG[A/G]AAACAAGggggctgg | 207259 |
rs6398090 | snp | C/T | 0.5 | 0 | intron-variant | Zbtb7c | Mm_Celera | 18:75924698 | ctcttccagaggtcc[C/T]gagttcaattcccag | 207259 |
rs6398586 | snp | C/T | 0.5 | 0 | intron-variant | Zbtb7c | GRCm38.p3 | 18:75924738 | agtgactcacaacca[C/T]ctgtaatgggatctg | 207259 |
rs6398664 | snp | A/G | 0.5 | 0 | intron-variant | Zbtb7c | GRCm38.p3 | 18:75924777 | ttctggtgtttctga[A/G]gacagcaacagtgta | 207259 |
rs6399159 | snp | A/G | 0.5 | 0 | intron-variant | Zbtb7c | Mm_Celera | 18:75924842 | ttTTTAAACGAGGAA[A/G]TGAGTATGATAAGCA | 207259 |
rs13483444 | snp | C/T | 0.4352 | 0.167931 | synonymous-codon | Zbtb7c | GRCm38.p3 | 18:76137589 | AAGACCCTCCTTATC[C/T]CCGTTTGCCCCGGAA | 207259 |
rs29535726 | snp | G/T | 0.375 | 0.216506 | intron-variant | Zbtb7c | Mm_Celera | 18:75862863 | AGGTAAAGGTGACAA[G/T]AGCACATCAGCTATT | 207259 |
rs29536454 | snp | A/T | 0.375 | 0.216506 | intron-variant | Zbtb7c | GRCm38.p3 | 18:75995918 | TGCCTCTGAGACCTC[A/T]TTTCTCTTATTCATT | 207259 |
rs29537251 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Zbtb7c | GRCm38.p3 | 18:76145333 | CCAGAGATCAAAGGG[C/T]TCCTGCTTCAGGAAG | 207259 |
rs29537996 | snp | A/G | 0.5 | 0 | intron-variant | Zbtb7c | GRCm38.p3 | 18:76037075 | CAGAGCCGAGGTTTG[A/G]GAGGGCCCTGGTTGT | 207259 |
rs29538168 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Zbtb7c | GRCm38.p3 | 18:75996433 | AGGAACTTGGCTTAC[A/G]AGAAGCGCTGACCCA | 207259 |
rs29538309 | snp | A/T | 0.495 | 0.0497494 | intron-variant | Zbtb7c | Mm_Celera | 18:75928764 | TCACATGGTCTCAGG[A/T]CCTGATGCGGCACCC | 207259 |
rs29539367 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Zbtb7c | GRCm38.p3 | 18:76026487 | CTTCTTTCTCTCATA[A/G]AGGAGGGTTATGTAC | 207259 |
rs29540913 | snp | C/T | 0.375 | 0.216506 | intron-variant | Zbtb7c | GRCm38.p3 | 18:75935321 | AGGAATTCACGAGGT[C/T]CGGATTTTTACCCTT | 207259 |
rs29541095 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Zbtb7c | GRCm38.p3 | 18:75837428 | GCCAGTGGTCTTAAC[C/G]GCTGAGCCAGCTCCC | 207259 |
rs29541711 | snp | A/T | 0.375 | 0.216506 | intron-variant | Zbtb7c | Mm_Celera | 18:75929307 | ACATTTGGGAAAAAG[A/T]CTTGGGGCTATTTCC | 207259 |
rs29541901 | snp | A/G | 0.375 | 0.216506 | intron-variant | Zbtb7c | Mm_Celera | 18:76123845 | TGCTGTTCTCTCCCT[A/G]TTCCCGTACTCTCCT | 207259 |
rs29541966 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Zbtb7c | GRCm38.p3 | 18:76111690 | CCACACCGATGGGCC[C/T]AGCTCTTTCCAGCTG | 207259 |
rs29543074 | snp | G/T | 0.32 | 0.24 | intron-variant | Zbtb7c | GRCm38.p3 | 18:76010990 | GTGACATGCTCAGGC[G/T]GAAGCAGAAGAATTC | 207259 |
rs29544021 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Zbtb7c | GRCm38.p3 | 18:76011861 | GTTGAAGGAGGATGC[C/T]CTGAGCCCTGTTCTG | 207259 |
rs29547858 | snp | G/T | 0.32 | 0.24 | intron-variant | Zbtb7c | Mm_Celera | 18:76104772 | CCTGCCCCTGCCCCT[G/T]CCCCTGCCCCTTCCC | 207259 |
rs29548494 | snp | A/T | 0.375 | 0.216506 | intron-variant | Zbtb7c | GRCm38.p3 | 18:75983906 | TTGGTTTGTGGGAAG[A/T]GTGCTTGGTTTCAGG | 207259 |
rs29550691 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Zbtb7c | Mm_Celera | 18:76144509 | AGGGGGCGTGCACCC[A/G]CGCACCTGACAGTGC | 207259 |
rs29550824 | snp | G/T | 0.49827 | 0.0293608 | intron-variant | Zbtb7c, LOC105246492 | GRCm38.p3 | 18:75960463 | TGACCGGTGGCATGG[G/T]CTTACCTGTGGTGGT | 207259 |
rs29550843 | snp | C/T | 0.375 | 0.216506 | intron-variant | Zbtb7c | GRCm38.p3 | 18:75976436 | CACACAGTTTGGAGT[C/T]TGAGCTGAAGCTAAA | 207259 |
rs29551478 | snp | A/T | 0.5 | 0 | intron-variant | Zbtb7c | GRCm38.p3 | 18:76050517 | GATCCCCGGGCTGTC[A/T]TTCTGGACCGCATGA | 207259 |
rs29551817 | snp | G/T | 0.456747 | 0.140554 | intron-variant | Zbtb7c | Mm_Celera | 18:75949792 | ATATGAGGGAGACAG[G/T]AAGGGCTACGCTGCC | 207259 |
rs29552887 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Zbtb7c | Mm_Celera | 18:75976339 | CCCGGGAGATAATCA[C/G]CTGGAAGGAGAAAGG | 207259 |
rs29553669 | snp | C/T | 0.32 | 0.24 | intron-variant | Zbtb7c | GRCm38.p3 | 18:76010892 | TGAGGTACAAGTCAG[C/T]AGAACGAGAGGGCAC | 207259 |
rs29553948 | snp | A/G | 0.5 | 0 | intron-variant | Zbtb7c | GRCm38.p3 | 18:75864205 | TTCAGGCCACAAATG[A/G]GCTTGAGGTTAGAAT | 207259 |
rs29554036 | snp | A/G | 0.32 | 0.24 | intron-variant | Zbtb7c | Mm_Celera | 18:75873976 | TTTATTGTGAACGGC[A/G]GCGTGCTCTGTGGGG | 207259 |
rs29554166 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Zbtb7c | GRCm38.p3 | 18:76048157 | GAATACAGCAGCTTT[C/T]GTTCTGTAAGTCCTG | 207259 |
rs29554334 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Zbtb7c | GRCm38.p3 | 18:75873826 | AAAGGAGTGAGGAGG[C/T]GAGTGAGCAAGAAGG | 207259 |
rs29554341 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Zbtb7c | GRCm38.p3 | 18:75917299 | GTGTCTGGGAGTGTT[C/T]ACAATCTGTGTGTTT | 207259 |
rs29554635 | snp | A/G | 0.32 | 0.24 | intron-variant | Zbtb7c | GRCm38.p3 | 18:76117697 | TGGAAAGGTGCCAGG[A/G]TTGAGCAATGCAGGG | 207259 |
rs29554687 | snp | A/C | 0.375 | 0.216506 | upstream-variant-2KB, nc-transcript-variant | Zbtb7c, Gm33703 | Mm_Celera | 18:75819670 | CGGTGTGAGCAGGTC[A/C]AGCCGGGCCGCAGAG | 207259 |
rs29555886 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Zbtb7c | GRCm38.p3 | 18:75870578 | CTTCATTTCAGATGT[C/T]GAAAATGTATATGCA | 207259 |
rs29555929 | snp | C/T | 0.5 | 0 | intron-variant | Zbtb7c | Mm_Celera | 18:76107968 | GATCTGGGATGGGGG[C/T]CTGGGTTCTAGGGCA | 207259 |
rs29556390 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Zbtb7c | GRCm38.p3 | 18:76064077 | TTTTCCAAGTTACAT[A/G]CATGCTTGATGCAAG | 207259 |
rs29556573 | snp | C/G | 0.5 | 0 | intron-variant | Zbtb7c | Mm_Celera | 18:76123448 | TCTGTCTGTGTCTGT[C/G]TGTGTGTGTGTGTGT | 207259 |
rs29556819 | snp | C/G | 0.444444 | 0.157135 | intron-variant, utr-variant-5-prime | Zbtb7c | GRCm38.p3 | 18:76059456 | CGCTCCAAACCACTC[C/G]TGGAATGGCTTAACT | 207259 |
rs29557200 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | Zbtb7c | GRCm38.p3 | 18:76056185 | CAGTAAGAGACACTA[A/C]ACTCATGTTCAGCAG | 207259 |
rs29557568 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Zbtb7c | Mm_Celera | 18:76100943 | CCTGAAGCCCCATTC[C/T]GTTACCCAGTCAAAG | 207259 |
rs29558195 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Zbtb7c | GRCm38.p3 | 18:76110253 | CTGACACAGAGGAGA[C/T]GCTCGCTCCTGAAAG | 207259 |
rs29558227 | snp | C/T | 0.375 | 0.216506 | intron-variant | Zbtb7c | GRCm38.p3 | 18:75865801 | GCGTGACATGGCTGT[C/T]GAGCACCTCAAGATG | 207259 |
rs29558441 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Zbtb7c | GRCm38.p3 | 18:75996990 | TTGTGTGGCCTCTGT[C/T]CATCCTATATCTAAC | 207259 |
rs29558872 | snp | G/T | 0.32 | 0.24 | intron-variant | Zbtb7c | GRCm38.p3 | 18:75992832 | CAAGGAAGACAAGCC[G/T]ATGGGAGGCACATTT | 207259 |
rs29558951 | snp | A/G | 0.46875 | 0.121031 | intron-variant, nc-transcript-variant | Zbtb7c, 2900057B20Rik | GRCm38.p3 | 18:76091914 | GTGTATCTGCTGACC[A/G]TTCCTTGGAAATAGC | 207259 |
rs29559042 | snp | A/C | 0.375 | 0.216506 | intron-variant | Zbtb7c | GRCm38.p3 | 18:76103954 | CTCCCAGGTACTGGG[A/C]AGCAGTGAGATTTTT | 207259 |
rs29559210 | snp | C/T | 0.5 | 0 | intron-variant | Zbtb7c, LOC105246492 | GRCm38.p3 | 18:75960194 | ACACTGCTCACCCCC[C/T]ACCCCCCAGGGCTCT | 207259 |
rs29560198 | snp | C/T | 0.375 | 0.216506 | intron-variant | Zbtb7c | GRCm38.p3 | 18:75984347 | GGGCCTGAGGGATAG[C/T]GAGCCGAGTGTGCCA | 207259 |
rs29560689 | snp | A/G | 0.375 | 0.216506 | intron-variant | Zbtb7c | GRCm38.p3 | 18:75894182 | GCAAGAGGGGCCAAG[A/G]GGGTTGCAAATCCAG | 207259 |
rs29560916 | snp | C/G | 0.32 | 0.24 | intron-variant | Zbtb7c | GRCm38.p3 | 18:76036448 | AACAGAGCTGGACCA[C/G]GGGCATCAGCAGCCA | 207259 |
rs29561658 | snp | A/C | 0.5 | 0 | intron-variant | Zbtb7c | Mm_Celera | 18:75866004 | CACCTGGAAGCCACT[A/C]GTTCATTCTTCATGT | 207259 |
rs29561696 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | Zbtb7c | GRCm38.p3 | 18:76053863 | CTTCTCTGGATGATT[G/T]CTGGGTACGTGGAGG | 207259 |
rs29562236 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Zbtb7c | GRCm38.p3 | 18:75864976 | GATAGCAAGGCCTTC[G/T]GGGCCTCTCCACGTG | 207259 |
rs29562299 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Zbtb7c | GRCm38.p3 | 18:75914688 | AGGAACAGGGAATTT[C/T]GCACCACCAGAGACT | 207259 |
rs29562940 | snp | A/G | 0.32 | 0.24 | intron-variant | Zbtb7c | GRCm38.p3 | 18:75969383 | AGAAATCAGAGCTAC[A/G]TATCCATAATATTAG | 207259 |
rs29563059 | snp | C/T | 0.32 | 0.24 | intron-variant | Zbtb7c | Mm_Celera | 18:75994698 | TGCAGGCTCTAATCT[C/T]TCTACTGTGTCTAGA | 207259 |
rs29563118 | snp | C/T | 0.375 | 0.216506 | intron-variant | Zbtb7c | GRCm38.p3 | 18:76125205 | CAGCCAAATACTAGG[C/T]GGTTCTCGTGGTAGA | 207259 |
rs29564286 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Zbtb7c, LOC105246492 | GRCm38.p3 | 18:75960431 | TGCTGTTCTTGTGAG[A/G]AGGGAATGTGGATAT | 207259 |
rs29564890 | snp | C/G | 0.375 | 0.216506 | intron-variant | Zbtb7c | GRCm38.p3 | 18:76012010 | TAAGTTTGCTCTTAG[C/G]TTGTCTCTATCAGAA | 207259 |
rs29565461 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Zbtb7c | GRCm38.p3 | 18:75863928 | CAATCTCCCCAAACC[C/T]GGGCATTAGTCAGAG | 207259 |