SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3719927 | snp | A/T | 0.5 | 0 | intron-variant | Wdr1 | GRCm38.p3 | 5:38546380 | GCACAGAGGTGAATG[A/T]CAGAGAAACTGAGGA | 22388 |
rs6232283 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Wdr1 | Mm_Celera | 5:38547943 | GTCGCTGCAGGGTTA[A/G]GGCTTCTTGGacctc | 22388 |
rs6232345 | snp | C/T | 0.5 | 0 | intron-variant | Wdr1 | Mm_Celera | 5:38547981 | cctcatttatagccc[C/T]tctgtaaaagcatta | 22388 |
rs6245283 | snp | A/G | 0.5 | 0 | intron-variant | Wdr1 | Mm_Celera | 5:38548018 | gggccatctcatggg[A/G]ttgctatgaggtcaa | 22388 |
rs6245909 | snp | A/G | 0.5 | 0 | intron-variant | Wdr1 | Mm_Celera | 5:38548137 | TCAGAGGCTCCCACT[A/G]CATGCAAACATGGGC | 22388 |
rs6245953 | snp | G/T | 0.5 | 0 | intron-variant | Wdr1 | Mm_Celera | 5:38548168 | CAATGTCTACAGcag[G/T]ggttctcaaccttcc | 22388 |
rs6246554 | snp | C/T | 0.5 | 0 | intron-variant | Wdr1 | GRCm38.p3 | 5:38548279 | tatttaattttgcta[C/T]tgttgtgantggaaa | 22388 |
rs6246915 | snp | A/G | 0.5 | 0 | intron-variant | Wdr1 | Mm_Celera | 5:38548288 | ttgctantgttgtga[A/G]tggaaangtaaatat | 22388 |
rs6246934 | snp | C/G | 0.5 | 0 | intron-variant | Wdr1 | Mm_Celera | 5:38548295 | tgttgtgantggaaa[C/G]gtaaatatctgtgtt | 22388 |
rs6247038 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Wdr1 | Mm_Celera | 5:38548346 | ccctCGGTTGAGAAC[C/T]GCTGGTCTAGAAGCA | 22388 |
rs13470843 | snp | A/G | | | utr-variant-3-prime | Wdr1 | Mm_Celera | 5:38527215 | GAATTTTTTTCTTTT[A/G]TTTTTTTTAATGTAT | 22388 |
rs13470844 | snp | C/G | 0.465374 | 0.126941 | synonymous-codon | Wdr1 | GRCm38.p3 | 5:38546988 | GGACATTGCCTGGAC[C/G]GAAGACAGTAAGAGG | 22388 |
rs13470845 | snp | C/T | | | synonymous-codon | Wdr1 | GRCm38.p3 | 5:38540016 | ACCCCTCCGGGTCAT[C/T]AAGGTAAGCCTTATT | 22388 |
rs13470846 | snp | C/T | 0.231111 | 0.249285 | missense | Wdr1 | Mm_Celera | 5:38535249 | TGTGAATGAGTCTGA[C/T]CAGTTGGTCAGCTGC | 22388 |
rs29507906 | snp | C/G | 0.375 | 0.216506 | intron-variant | Wdr1 | GRCm38.p3 | 5:38532554 | CAGGGACTTCAGAGA[C/G]TCAGAAGCTAACGTG | 22388 |
rs29558651 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Wdr1 | GRCm38.p3 | 5:38528248 | GCTGTACTCGACAGA[A/C]ATGACAGCCATGCTC | 22388 |
rs29563008 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Wdr1 | GRCm38.p3 | 5:38551579 | TTTAACATCCGACAA[C/T]CATGGCCAAAGTCCT | 22388 |
rs29568552 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr1 | GRCm38.p3 | 5:38553400 | AGGAAAACTAGGAAC[A/G]ATAGATTCTCCCACC | 22388 |
rs29579421 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr1 | GRCm38.p3 | 5:38549849 | TTTTCCTAAGCTTTC[C/T]CATCCCCTCCCTTCC | 22388 |
rs29628714 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Wdr1 | GRCm38.p3 | 5:38558264 | TGCAGAGAATTTATT[C/T]TTCAAGCGTGGCAAC | 22388 |
rs29679816 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Wdr1 | GRCm38.p3 | 5:38543943 | GCCTAGTCTGAGAGA[A/G]TACACTGGCACACTG | 22388 |
rs29728591 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Wdr1 | GRCm38.p3 | 5:38553604 | TATGCTTGGTAGAAG[C/T]CAGGGAGTGTTCTGG | 22388 |
rs29771601 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr1 | GRCm38.p3 | 5:38533124 | TCCTCCAGGGTTCCC[A/G]CTTTGAGTTCCTGCC | 22388 |
rs29773793 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Wdr1 | GRCm38.p3 | 5:38543177 | CACCTTACCTCTCAG[C/T]CTGTTATAAGCTCTG | 22388 |
rs29776143 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr1 | GRCm38.p3 | 5:38528679 | CCCAGCCTGGCTCAG[C/T]AGCCCCATTATCAAG | 22388 |
rs32684074 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdr1 | Mm_Celera | 5:38537452 | ACCTACCTGGGCTAA[A/G]AACAAGGTCTATATC | 22388 |
rs32684076 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr1 | Mm_Celera | 5:38537360 | ACAGGTAAGTCCCGA[A/G]CCACTCACTATCAGT | 22388 |
rs32684078 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr1 | Mm_Celera | 5:38537328 | GCTGTGCTTGGTCTC[C/T]AGCAGACACACTGCC | 22388 |
rs32684080 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Wdr1 | Mm_Celera | 5:38536851 | ACTCAATGATTTCAT[A/T]GCCAGTGACAGAGCT | 22388 |
rs32684082 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Wdr1 | Mm_Celera | 5:38536636 | GCAGGCAGGCCTCAA[A/T]CAGTTACATACTTCC | 22388 |
rs32684084 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdr1 | Mm_Celera | 5:38543526 | GAATTCCTCAGAACC[A/G]CTACACCTCTAGCTT | 22388 |
rs32684086 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr1 | Mm_Celera | 5:38543383 | GTTAGGAATGAAAGA[C/T]CTAGTGACAAAGGGC | 22388 |
rs32684088 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Wdr1 | Mm_Celera | 5:38543361 | ACCAAGTTCCCAGCA[G/T]TCACAGGTTAGGAAT | 22388 |
rs32684090 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Wdr1 | GRCm38.p3 | 5:38543349 | GAAGTGAAGGCAACC[A/C]AGTTCCCAGCATTCA | 22388 |
rs32684093 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr1 | GRCm38.p3 | 5:38542980 | CTTATCTTTCTCTCA[A/G]CTACTATTTACCTTC | 22388 |
rs32684094 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr1 | Mm_Celera | 5:38556315 | AAGGTAACAAGTCCA[A/G]TATCAAAGCTGGGAA | 22388 |
rs32684095 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Wdr1 | GRCm38.p3 | 5:38556270 | GAAGGTAGAAATGGT[A/T]ACAGAGGTGAGACAG | 22388 |
rs32684097 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Wdr1 | GRCm38.p3 | 5:38555699 | TAAACTAATGCTTAG[C/T]TGAATAAGCCAAGGC | 22388 |
rs32684098 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr1 | Mm_Celera | 5:38555449 | TTTAGCACATGGCAC[C/T]GGTCCACTTGTCCTT | 22388 |
rs32684099 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr1 | Mm_Celera | 5:38555386 | ACTGCTTCAAAGTCC[A/G]CCTACTTCCATTAAA | 22388 |
rs32684100 | snp | A/G/T | 0.444444 | 0.157135 | intron-variant | Wdr1 | GRCm38.p3 | 5:38555281 | ACCAAACAGCACACC[A/G/T]TCCCTGGCTCCATAA | 22388 |
rs32684101 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Wdr1 | Mm_Celera | 5:38555264 | AACCTGACTGGGAAG[C/T]CACCAAACAGCACAC | 22388 |
rs32684102 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Wdr1 | GRCm38.p3 | 5:38554426 | GAAGCCTCCACAAGG[C/T]GTTCCTCATCCTTGA | 22388 |
rs32684765 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr1 | Mm_Celera | 5:38542933 | CCAAATTGGACAAGC[A/G]AGTTGGATACGGTAT | 22388 |
rs32684767 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Wdr1 | Mm_Celera | 5:38542808 | GAACAACACTCAAGT[A/C]TGGTAGTGGGGTCTG | 22388 |
rs32684769 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr1 | Mm_Celera | 5:38542731 | AAGTCATCTACTACA[C/T]CTAAAAAAAACTACA | 22388 |
rs32684771 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr1 | Mm_Celera | 5:38542707 | ACCCTATGACCTACG[A/G]CCCTCTTAAAGTCAT | 22388 |
rs32684773 | snp | A/T | 0.197531 | 0.244432 | intron-variant | Wdr1 | Mm_Celera | 5:38542625 | GGCAATGACAGGGAT[A/T]GCCAGCAACAAGGAG | 22388 |
rs32684784 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr1 | Mm_Celera | 5:38536574 | GAGGTCATCATGCAG[A/G]GCCAGCTTCACAGTG | 22388 |
rs32684786 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wdr1 | Mm_Celera | 5:38536313 | CCTAGACATGGGCAC[C/T]AAGGTTCATGTGTGA | 22388 |
rs32684788 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr1 | Mm_Celera | 5:38536261 | CTTTCAAGTGACCAC[C/T]ATCATTTCTGTGACA | 22388 |
rs32684790 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdr1 | Mm_Celera | 5:38535979 | AGTGACCAGAGTACC[A/G]TGTGCAGAGAACAGT | 22388 |
rs32684791 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Wdr1 | Mm_Celera | 5:38535930 | TAGCATCACTGACTA[A/C]TCCTGGAGCAGCCTT | 22388 |
rs32684792 | snp | C/G | 0.32 | 0.24 | intron-variant | Wdr1 | Mm_Celera | 5:38535572 | TTCTTAAGAATGCAT[C/G]CAAGGCCAATGTATT | 22388 |
rs32685234 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Wdr1 | Mm_Celera | 5:38554423 | TCAGAAGCCTCCACA[A/G]GGTGTTCCTCATCCT | 22388 |
rs32685235 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr1 | Mm_Celera | 5:38553686 | CCTGCAACTACAGCA[C/T]ACCTCACAAAGCACC | 22388 |
rs32685236 | snp | G/T | 0.456747 | 0.140554 | intron-variant | Wdr1 | GRCm38.p3 | 5:38553646 | TGGTGCTATGGTCAT[G/T]GAACTAGTCAGGTCA | 22388 |
rs32685238 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Wdr1 | GRCm38.p3 | 5:38553612 | GTAGAAGCCAGGGAG[C/T]GTTCTGGAATCCTGG | 22388 |
rs32685241 | snp | C/G/T | 0.132653 | 0.220748 | intron-variant | Wdr1 | GRCm38.p3 | 5:38552497 | TGCTTCATATGACAG[C/G/T]CCATGAGCCATCACA | 22388 |
rs32685375 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Wdr1 | GRCm38.p3 | 5:38542338 | CAAGAAAACAAGCTT[C/G]AAGTAGACACTCTAA | 22388 |
rs32685377 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Wdr1 | GRCm38.p3 | 5:38542150 | GGGTTACATTTAATC[G/T]TACAGGTCCAGTCTC | 22388 |
rs32685379 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Wdr1 | GRCm38.p3 | 5:38542114 | GACAAGACTTCTGAT[C/G]CCTGGCCCAGCCGTC | 22388 |
rs32685381 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Wdr1 | GRCm38.p3 | 5:38542054 | CTGAGTCCAGAGGTT[A/C]AGCCACCTCACATGG | 22388 |
rs32685383 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr1 | GRCm38.p3 | 5:38541956 | TAACAGCAGCCCATT[A/G]GCCAAAGAAAATGAG | 22388 |
rs32685430 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Wdr1 | Mm_Celera | 5:38558379 | ACAGCTGACAGGCAG[C/T]CCCAGCAGGAGGCTG | 22388 |
rs32685432 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr1 | Mm_Celera | 5:38558353 | TCACAAAGCCGTCTT[C/T]CAGTCACAGAACAGC | 22388 |
rs32685594 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr1 | Mm_Celera | 5:38535475 | GGATGGCCAACTTTG[A/G]GATTTCAGTGAGCAA | 22388 |
rs32686115 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr1 | Mm_Celera | 5:38541937 | CTGTGTGGCAGGGAA[C/T]AGGTAACAGCAGCCC | 22388 |
rs32686117 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr1 | Mm_Celera | 5:38541891 | CTCAGCCAGGCATGG[A/G]CAAGAGACATGTCTG | 22388 |
rs32686119 | snp | C/T | 0.5 | 0 | intron-variant | Wdr1 | GRCm38.p3 | 5:38541538 | TGTGAAAGGAACATG[C/T]CATGAAAGGAACATT | 22388 |
rs32686121 | snp | G/T | 0.396694 | 0.202437 | intron-variant | Wdr1 | GRCm38.p3 | 5:38541521 | GTGCCAACTCATCAC[G/T]GTGTGAAAGGAACAT | 22388 |
rs32686123 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr1 | Mm_Celera | 5:38541417 | GCCTGTCCCACAGAA[A/G]GCAAGCAAAGGAGCC | 22388 |
rs32686144 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Wdr1 | Mm_Celera | 5:38550968 | AAACTGAATGAATGA[C/G]TCGAGTGAATAAATG | 22388 |
rs32686146 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr1 | Mm_Celera | 5:38550966 | AAAAACTGAATGAAT[A/G]ACTCGAGTGAATAAA | 22388 |
rs32686148 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Wdr1 | GRCm38.p3 | 5:38550775 | GCCTGCCATATCAGA[C/T]ACACTGCCTGAGGGA | 22388 |
rs32686150 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr1 | GRCm38.p3 | 5:38550178 | GGTCTAGGTCCACAG[A/G]CACTCAGATAGGGAT | 22388 |
rs32686152 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Wdr1 | GRCm38.p3 | 5:38550032 | AACCAGGGCTGTTAA[A/G]AGAACATCAAAACCA | 22388 |
rs32686205 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr1 | Mm_Celera | 5:38558066 | TCCACTTGGTCCAAA[A/G]AGACGAGCCAGTGGT | 22388 |
rs32686207 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Wdr1 | Mm_Celera | 5:38558016 | GGGCTGGTAACAGAT[A/G]GTGCCAAATGAAAAC | 22388 |
rs32686211 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr1 | Mm_Celera | 5:38557931 | GCACCTGGACAGAGC[A/G]ACTGTTAAGTCTTCG | 22388 |
rs32686213 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Wdr1 | Mm_Celera | 5:38557801 | AAACACACTACCACA[G/T]TCTGCTACAAAGAAC | 22388 |
rs32686905 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Wdr1 | GRCm38.p3 | 5:38541333 | TAAGGCAGGCCAGGG[C/T]AATCCCCAGTCTTGG | 22388 |
rs32686906 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Wdr1 | Mm_Celera | 5:38541146 | AAGTGCCTCCTGATG[C/T]GTCCTCTTCCCACTG | 22388 |
rs32686908 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Wdr1 | GRCm38.p3 | 5:38541106 | TGGAAGGCCATCCTT[C/T]AGCCAGGTCTGCCTC | 22388 |
rs32686910 | snp | A/C | 0.459184 | 0.136902 | intron-variant | Wdr1 | Mm_Celera | 5:38541080 | TGTTCCTGCCTGGTC[A/C]CTGCTCTATCTGGAA | 22388 |
rs32686912 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr1 | GRCm38.p3 | 5:38540889 | TGGTCCTGTGGGAGA[A/G]AGGGCTGTCACTAAC | 22388 |
rs32687004 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr1 | Mm_Celera | 5:38557436 | GTTACAGCCTCTTCT[C/T]TAGCTTTACTCAATG | 22388 |
rs32687006 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr1 | Mm_Celera | 5:38557397 | GTCTAGCTGCCAACT[C/T]GAGTCATGTCCCTCA | 22388 |
rs32687007 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr1 | Mm_Celera | 5:38557319 | CTACATAGAGAAACC[C/T]GATGTGACAAACCTA | 22388 |
rs32687008 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Wdr1 | Mm_Celera | 5:38557088 | TTTATGCCCAGCTTG[A/C]TAATGGGTTTCCCAG | 22388 |
rs32687010 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr1 | Mm_Celera | 5:38557054 | CAGCTACCTAGATGA[C/T]GAGCCTTTGAGCAAT | 22388 |
rs32687011 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr1 | Mm_Celera | 5:38557006 | GACACCCTGGCTTTG[C/T]GGATATGTACTAGAA | 22388 |
rs32687013 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Wdr1 | Mm_Celera | 5:38557004 | ATGACACCCTGGCTT[A/T]GTGGATATGTACTAG | 22388 |
rs32687044 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr1 | Mm_Celera | 5:38548891 | ACCCTGGGTTGATGG[A/G]CCAGCTGCTACCCCT | 22388 |
rs32687045 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr1 | Mm_Celera | 5:38548575 | CCAGAAAGGAAAGTG[C/T]GAAGCGAGCAGTATG | 22388 |
rs32687047 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Wdr1 | GRCm38.p3 | 5:38548529 | TGTTCCAGAAAGAAA[C/T]GGAGACCTGGTTAGT | 22388 |
rs32687049 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Wdr1 | Mm_Celera | 5:38548498 | TGATGTCCAGGAAGA[C/T]AGCAGTGCTGAGGCG | 22388 |
rs32687053 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Wdr1 | Mm_Celera | 5:38547874 | CTTTTTGGGCTAAAC[A/C]GAGGTGATAGGCAAT | 22388 |
rs32687634 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wdr1 | GRCm38.p3 | 5:38540725 | TCTGCTGGGCTTTGG[C/T]AGCACCCTAGAAGTG | 22388 |
rs32687636 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr1 | Mm_Celera | 5:38540620 | ATGTAGAAGCTGGTG[C/T]CATGTGCTATTAGCC | 22388 |