SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3689328 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Ankfy1 | Mm_Celera | 11:72703397 | TTTGTGTAGTACCAT[C/T]AGTACAGTCTTCACG | 11736 |
rs3712585 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ankfy1 | Mm_Celera | 11:72747807 | ATGGTGCCTGTGCTA[C/T]GTGCCTGCCGGTCTC | 11736 |
rs3724115 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Ankfy1 | Mm_Celera | 11:72760534 | TAGAGATAAAATGTA[A/T]CCAAGATTCGGGAGG | 11736 |
rs6185715 | snp | A/G | 0.5 | 0 | intron-variant | Ankfy1 | Mm_Celera | 11:72737191 | ACTCTGAGAAGAGAG[A/G]TTAGCATCTGAGATC | 11736 |
rs6200167 | snp | C/T | 0.5 | 0 | intron-variant | Ankfy1 | Mm_Celera | 11:72737653 | gtgcgccaccacacc[C/T]ggcCTTGAGGCCAAG | 11736 |
rs6201094 | snp | C/G | 0.5 | 0 | intron-variant | Ankfy1 | GRCm38.p3 | 11:72737800 | tgtgtgtgtgtgtgt[C/G]tgtgtgtgtgtgtgt | 11736 |
rs6233464 | snp | C/T | 0.5 | 0 | intron-variant | Ankfy1 | Mm_Celera | 11:72745666 | GTTACACAGAAAGCC[C/T]NCTCCTTACTCAGCC | 11736 |
rs6233466 | snp | A/T | 0.5 | 0 | intron-variant | Ankfy1 | Mm_Celera | 11:72745667 | TTACACAGAAAGCCN[A/T]CTCCTTACTCAGCCC | 11736 |
rs6233495 | snp | C/T | 0.5 | 0 | intron-variant | Ankfy1 | Mm_Celera | 11:72745687 | TTACTCAGCCCTCTC[C/T]GTGGCACTGTTTTGT | 11736 |
rs6233975 | snp | G/T | 0.5 | 0 | intron-variant | Ankfy1 | Mm_Celera | 11:72745751 | TCATATTTATTTTAT[G/T]TAGATTTTCAAGCAC | 11736 |
rs6391388 | snp | A/G | 0.5 | 0 | intron-variant | Ankfy1 | Mm_Celera | 11:72727268 | GTATACTGTGGTCTG[A/G]tgtgtgtgtgtgtgt | 11736 |
rs6391444 | snp | A/T | 0.5 | 0 | intron-variant | Ankfy1 | GRCm38.p3 | 11:72727297 | gtgtgtgtgtgtgtg[A/T]gATACTNAGGATTGA | 11736 |
rs6391448 | snp | A/G | 0.5 | 0 | intron-variant | Ankfy1 | Mm_Celera | 11:72727304 | tgtgtgtgngATACT[A/G]AGGATTGAATCCACA | 11736 |
rs13474053 | snp | A/G | | | utr-variant-3-prime | Ankfy1 | Mm_Celera | 11:72770492 | CCCCCATACTGAACC[A/G]TTCCTGTACTAGTCT | 11736 |
rs13474054 | snp | C/T | | | utr-variant-3-prime | Ankfy1 | Mm_Celera | 11:72770158 | TAACACAGCAATGTC[C/T]CACAAGCTTAAGTGC | 11736 |
rs13474056 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Ankfy1 | Mm_Celera | 11:72770775 | ATAGTGAAAAACCAG[C/T]TAACTAAATATAAAA | 11736 |
rs26887821 | snp | A/G | 0.391111 | 0.206368 | downstream-variant-500B | Ankfy1 | GRCm38.p3 | 11:72772417 | GTCAGTCCAGTGTGA[A/G]ACTGATGGATATGTG | 11736 |
rs26887822 | snp | C/T | 0.32 | 0.24 | downstream-variant-500B | Ankfy1 | GRCm38.p3 | 11:72772173 | ACTAATGTGTTCTTT[C/T]TCTACTGTTCTTATA | 11736 |
rs26887823 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime, downstream-variant-500B | Ankfy1 | Mm_Celera | 11:72771696 | ATGCAGAATCAGCTG[C/T]CTGACACCATGGAAG | 11736 |
rs26887824 | snp | C/G | 0.32 | 0.24 | utr-variant-3-prime, downstream-variant-500B | Ankfy1 | Mm_Celera | 11:72771597 | ACTGACAGACCTCAC[C/G]AGCGTTCTGTGCAGA | 11736 |
rs26887825 | snp | G/T | 0.33241 | 0.236027 | utr-variant-3-prime | Ankfy1 | Mm_Celera | 11:72770594 | TGAACTGCCAAATGC[G/T]TAGGAGAGGAAGCAA | 11736 |
rs26887826 | snp | A/G | 0.336735 | 0.234472 | utr-variant-3-prime | Ankfy1 | Mm_Celera | 11:72769997 | ATCAAGTTTACTGAA[A/G]CATAATTGCTGCATC | 11736 |
rs26887827 | snp | C/G | 0.33241 | 0.236027 | utr-variant-3-prime | Ankfy1 | Mm_Celera | 11:72769882 | CCATGAAATTGCTTA[C/G]CTGTTCTTGTTCGGT | 11736 |
rs26887828 | snp | C/T | 0.33241 | 0.236027 | utr-variant-3-prime | Ankfy1 | Mm_Celera | 11:72769606 | AACTGTACTTACAAT[C/T]TGCAGATGATGCCTA | 11736 |
rs26887829 | snp | A/G | 0.459184 | 0.136902 | utr-variant-3-prime | Ankfy1 | Mm_Celera | 11:72769510 | ATGAACCAGGGTGGA[A/G]AGGGCACATAGGGAA | 11736 |
rs26887830 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Ankfy1 | Mm_Celera | 11:72769433 | CCTAAAAAGGGCCAC[A/G]AAGACCTAGAGTTAG | 11736 |
rs26887831 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Ankfy1 | Mm_Celera | 11:72769059 | CATTTGATAACCCTA[C/T]GATACTTGCGTTAAT | 11736 |
rs26887832 | snp | C/T | 0.132653 | 0.220748 | utr-variant-3-prime | Ankfy1 | Mm_Celera | 11:72768917 | CACTGAAAGAGAAAC[C/T]TACACCACTGGGTTT | 11736 |
rs26887833 | snp | G/T | 0.244898 | 0.249948 | utr-variant-3-prime | Ankfy1 | Mm_Celera | 11:72768393 | AATGCACTTTGACTG[G/T]GCTGCACTTTTCTAG | 11736 |
rs26887834 | snp | A/G | 0.33241 | 0.236027 | utr-variant-3-prime | Ankfy1 | Mm_Celera | 11:72768351 | GTCTTTGGAGTCCTC[A/G]GTCGCTGCCACTTGA | 11736 |
rs26887835 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Ankfy1 | Mm_Celera | 11:72768330 | TCTCTCGTCTTGCTG[C/T]GTCCTGTCTTTGGAG | 11736 |
rs26887836 | snp | A/C | 0.32 | 0.24 | intron-variant | Ankfy1 | Mm_Celera | 11:72767330 | AGCGTCTGTGCTTAA[A/C]TTCTTCCTGTTTGCT | 11736 |
rs26887837 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Ankfy1 | Mm_Celera | 11:72764935 | ACTTCCATACTTGTC[C/T]ACAGTGAGCCATGAA | 11736 |
rs26887838 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Ankfy1 | Mm_Celera | 11:72764659 | CTCTGTGAAGCTAGA[A/G]GAGTTGGAATGTCAC | 11736 |
rs26887839 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Ankfy1 | Mm_Celera | 11:72764519 | CCTTCAGCCTTGCCA[A/G]GTTTTCTGTGGTGTG | 11736 |
rs26887840 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Ankfy1 | Mm_Celera | 11:72764354 | CCATCTCTCTGTTGG[A/T]CCCACCAGACTGAGT | 11736 |
rs26887841 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ankfy1 | Mm_Celera | 11:72764243 | GTGTGACTAACCCAC[C/T]TGCCACTTCTCCCTG | 11736 |
rs26887842 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Ankfy1 | Mm_Celera | 11:72764187 | GCTATACACTTGGTC[A/G]GTCTTTCCAGCACTC | 11736 |
rs26887843 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ankfy1 | Mm_Celera | 11:72764163 | ATATGTAGTCTTAAT[C/T]TTTCCTATGCTATAC | 11736 |
rs26887844 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Ankfy1 | Mm_Celera | 11:72764128 | GTGTAAACATTTTTT[G/T]GGAAAGCTTTGTACT | 11736 |
rs26887845 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ankfy1 | Mm_Celera | 11:72760713 | AGGAACATCATTGCC[C/T]GGGATGTAGCATAAG | 11736 |
rs26887846 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Ankfy1 | Mm_Celera | 11:72760009 | CCTTTAATCTGAGGT[A/G]AGTGTGGCTAGCTGA | 11736 |
rs26887847 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ankfy1 | Mm_Celera | 11:72758302 | TTGCTGTGTTTGCCT[C/T]AGTAGGAAGGTGTGC | 11736 |
rs26887848 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Ankfy1 | Mm_Celera | 11:72757654 | AGAGTCAGGCCTTGA[A/G]AGCCAAGGAGGATTT | 11736 |
rs26887849 | snp | C/T | 0.197531 | 0.244432 | synonymous-codon | Ankfy1 | Mm_Celera | 11:72757442 | CCTTGCTGTTCAGGC[C/T]GGCTCAGAGATCATT | 11736 |
rs26887850 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Ankfy1 | Mm_Celera | 11:72757095 | TTGGCTTTCCATGGC[C/T]GGTTCCTATTGTAGG | 11736 |
rs26887851 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ankfy1 | Mm_Celera | 11:72756593 | TAAGTTGCCCTTAAC[A/G]TTAAGTTTGCCCATA | 11736 |
rs26887852 | snp | A/T | 0.35503 | 0.226867 | intron-variant | Ankfy1 | Mm_Celera | 11:72756505 | GGCCTGCATACAATG[A/T]AGTGCTGGCATAAAG | 11736 |
rs26887853 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Ankfy1 | Mm_Celera | 11:72756170 | CTCTCTGCATTTGCC[A/G]CATGCTTTAATAAGG | 11736 |
rs26887854 | snp | A/G | 0.359862 | 0.224567 | synonymous-codon | Ankfy1 | Mm_Celera | 11:72755854 | CAATAAGGCAGCTGA[A/G]GCCATTTTAAAACGA | 11736 |
rs26887855 | snp | A/C | 0.359862 | 0.224567 | intron-variant | Ankfy1 | Mm_Celera | 11:72755568 | TTTTATGCCTCTTTA[A/C]AAACTGATTTCAAAC | 11736 |
rs26887856 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Ankfy1 | Mm_Celera | 11:72754682 | CTGTGCCTTGTTCTT[C/T]AGCATAAAGGTTGTT | 11736 |
rs26887857 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Ankfy1 | Mm_Celera | 11:72754633 | AGTAGTCATATAGCC[C/T]GTCTGGTAATTGAAT | 11736 |
rs26887858 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Ankfy1 | Mm_Celera | 11:72754246 | GGCTAGCAGGGTGTG[A/G]CGATGAAGGCTTTGT | 11736 |
rs26887859 | snp | G/T | 0.290657 | 0.246672 | intron-variant | Ankfy1 | Mm_Celera | 11:72754132 | TTCTCAAAGTTTAAG[G/T]CTGCAACAGTTCTGA | 11736 |
rs26887860 | snp | A/G | 0.345679 | 0.230967 | missense | Ankfy1 | Mm_Celera | 11:72753675 | CTTCTGCATAGAGCC[A/G]TTGATGAAAACAATG | 11736 |
rs26887861 | snp | A/T | 0.32 | 0.24 | intron-variant | Ankfy1 | Mm_Celera | 11:72753112 | ACTTTGGAGTACACA[A/T]AGTCACAGGAACTGT | 11736 |
rs26887862 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ankfy1 | Mm_Celera | 11:72752778 | GCAGTGTGAGATTCA[C/T]GTTGGTGCGGCCAGC | 11736 |
rs26887863 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Ankfy1 | Mm_Celera | 11:72752018 | CTTTCTTTGGCTGCC[A/G]TTAGAAGCACTGGTT | 11736 |
rs26887864 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Ankfy1 | Mm_Celera | 11:72751912 | AGCCAGCAGGTTTGA[C/T]TTTCTTGAGAGCATT | 11736 |
rs26887865 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ankfy1 | Mm_Celera | 11:72751182 | GTACTCTGTCCTTCT[C/T]GGTAACTGTCAGGGC | 11736 |
rs26887866 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Ankfy1 | Mm_Celera | 11:72751115 | TCTGTTATAAAAAGT[A/G]CAGACACGGGTTATA | 11736 |
rs26887867 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Ankfy1 | Mm_Celera | 11:72751043 | TGATGGGGTAGCTCA[A/G]TGATAGGGCACTTGT | 11736 |
rs26887868 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Ankfy1 | Mm_Celera | 11:72750962 | GGAACATAGCACTTA[A/G]GTAGAGAGCTCTGAC | 11736 |
rs26887869 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Ankfy1 | Mm_Celera | 11:72750725 | CAGGACTGGATGCAC[A/G]CCTATAATGTCATCT | 11736 |
rs26887870 | snp | C/T | 0.32 | 0.24 | intron-variant | Ankfy1 | Mm_Celera | 11:72750371 | AGGAAAAGATGGTAA[C/T]GCATGGGCTGGGGCT | 11736 |
rs26887871 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Ankfy1 | Mm_Celera | 11:72750318 | GGAAAAGCGCTGTCT[C/T]GGAGAAGCGTCGAGG | 11736 |
rs26887872 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ankfy1 | Mm_Celera | 11:72749786 | AATATCTGTTGGCTC[C/T]CTCTAAAAAGCAATC | 11736 |
rs26887873 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Ankfy1 | Mm_Celera | 11:72749644 | TAGTTTTGTAGCTGT[C/T]ACTTACATTGTAGTC | 11736 |
rs26887874 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ankfy1 | Mm_Celera | 11:72749532 | TAGAGCAGAAAGGTA[A/G]GTAGTTGGGTCTGAT | 11736 |
rs26887875 | snp | A/G | 0.401235 | 0.199068 | missense | Ankfy1 | Mm_Celera | 11:72749447 | ATGAGTTCTGCAGAC[A/G]GCATCTACCTACAAA | 11736 |
rs26887876 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ankfy1 | Mm_Celera | 11:72748948 | CCATAATTCTGTTGT[C/T]TTCTAGTGTTGATTG | 11736 |
rs26887877 | snp | A/C | 0.32 | 0.24 | intron-variant | Ankfy1 | Mm_Celera | 11:72745367 | GCATAGGTTAGCCAG[A/C]CCTAGAGTTTCCCTT | 11736 |
rs26887878 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Ankfy1 | Mm_Celera | 11:72744872 | ATTAGTATGTAGTTG[C/T]GATGGCATTTCCAGG | 11736 |
rs26887879 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Ankfy1 | Mm_Celera | 11:72744850 | TGTCATATACCACCA[C/T]TTCTAGATTAGTATG | 11736 |
rs26887880 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ankfy1 | Mm_Celera | 11:72743807 | GAACTTGAATTTTGA[A/G]TTTTGTTGCATTACT | 11736 |
rs26887881 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Ankfy1 | Mm_Celera | 11:72743371 | TTCTAGCCAGCTTGG[A/G]CAATATAGCAACTTG | 11736 |
rs26887882 | snp | A/T | 0.493827 | 0.0552116 | intron-variant | Ankfy1 | Mm_Celera | 11:72741617 | TTCTCTGCATCTGTG[A/T]ATGAAGTGTATGAAG | 11736 |
rs26887883 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Ankfy1 | Mm_Celera | 11:72739801 | ACATTGCTCCAGGAC[A/G]GGGTTAGAATTGGGG | 11736 |
rs26887884 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Ankfy1 | Mm_Celera | 11:72739612 | TAGTGCTCTAGTGTC[A/G]GCCTTCCCTGCAGGC | 11736 |
rs26887885 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Ankfy1 | Mm_Celera | 11:72739436 | ATAAGATGGTCCAGG[A/G]TCTTTGTGTCACAAT | 11736 |
rs26887886 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Ankfy1 | Mm_Celera | 11:72738802 | TTTATCTCTGTGAGG[C/T]CAAATGGTTAGAAAA | 11736 |
rs26887887 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Ankfy1 | Mm_Celera | 11:72738099 | GAATAACTCTGGACT[A/G]TCATCGGTTTCCACC | 11736 |
rs26887888 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Ankfy1 | Mm_Celera | 11:72736432 | TGTTTGCAGTAAGGA[A/G]CTTCTGACTCCCTCA | 11736 |
rs26887889 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ankfy1 | Mm_Celera | 11:72736202 | GATTTCCTAAATGGG[C/T]TTCTCCTGACCAATT | 11736 |
rs26887890 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Ankfy1 | Mm_Celera | 11:72735652 | AAACACAGTGGCCTT[C/T]ACCTTGCCCGAGCAG | 11736 |
rs26887891 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ankfy1 | Mm_Celera | 11:72735567 | GATCTTTCTGCTTTA[C/G]CAGGCTTTTAGCACA | 11736 |
rs26887892 | snp | G/T | 0.165289 | 0.235211 | intron-variant | Ankfy1 | Mm_Celera | 11:72735136 | TTCATTGGGGAAAGT[G/T]TCTACCCCGTAGGGA | 11736 |
rs26887893 | snp | C/T | 0.387812 | 0.208586 | synonymous-codon | Ankfy1 | Mm_Celera | 11:72730618 | GATTGAAATGGATTC[C/T]CAGGTATTGTAGAAG | 11736 |
rs26887894 | snp | C/T | 0.18 | 0.24 | intron-variant | Ankfy1 | Mm_Celera | 11:72729227 | CATAAATAACAGGTT[C/T]TACATTTCTTCGTTA | 11736 |
rs26887895 | snp | A/C | 0.359862 | 0.224567 | intron-variant | Ankfy1 | Mm_Celera | 11:72729199 | TCCACTGCTTCACTT[A/C]TTGGGTTTCCATCAT | 11736 |
rs26887896 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Ankfy1 | Mm_Celera | 11:72729081 | CTAGAGTGGAACAGG[A/C]AGAGATGGCTAAGGT | 11736 |
rs26887897 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Ankfy1 | Mm_Celera | 11:72728919 | GTATGGACAAGCCTT[C/T]ACACTGCAGCTGGAG | 11736 |
rs26887898 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Ankfy1 | Mm_Celera | 11:72728289 | TCTGTTTTGTGTTTG[A/G]CTTTAGAATGGCCTG | 11736 |
rs26887899 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Ankfy1 | Mm_Celera | 11:72726311 | GGAACACTTAATTCC[A/G]TAGCTGTGGTCAGGT | 11736 |
rs26887900 | snp | C/G | 0.33241 | 0.236027 | intron-variant | Ankfy1 | Mm_Celera | 11:72726251 | TGCTGCTAGGACACT[C/G]TTATAGCAAGACTAG | 11736 |
rs26887901 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ankfy1 | Mm_Celera | 11:72726227 | TGCAGTCCTATGAGG[C/T]GGGCCACCTGCTGCT | 11736 |
rs26887902 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ankfy1 | Mm_Celera | 11:72724143 | AGCCAGTAGGCTCTG[A/G]CAAAACCATGCAGTT | 11736 |
rs26887903 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Ankfy1 | Mm_Celera | 11:72723232 | GGTGCATTTTCTTTG[G/T]TCCTCTCTGAAGTTA | 11736 |
rs26887904 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Ankfy1 | Mm_Celera | 11:72722577 | AAGCACAGATTTTAG[A/G]GTTACTTCTAGAAGG | 11736 |