SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13481953 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Wdr41 | Mm_Celera | 13:95008925 | TGTATACATACACGT[A/G]TACCAGGAAGACAGA | 218460 |
rs29222778 | snp | G/T | 0.375 | 0.216506 | intron-variant | Wdr41 | Mm_Celera | 13:95004935 | CTTCTGTCCATTGGT[G/T]GGGTGCAAATACCTG | 218460 |
rs29236269 | snp | A/T | 0.456747 | 0.140554 | intron-variant | Wdr41 | Mm_Celera | 13:94990762 | TCAGAGCTGAGAGGC[A/T]GAGTGATCAACAAAG | 218460 |
rs29240785 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr41 | Mm_Celera | 13:95004938 | CTGTCCATTGGTTGG[A/G]TGCAAATACCTGCAT | 218460 |
rs29242494 | snp | C/T | 0.5 | 0 | intron-variant | Wdr41 | Mm_Celera | 13:94990342 | TCAGTTCTCAGCACC[C/T]ACATAGTAGTTCACA | 218460 |
rs29246310 | snp | C/G | 0.188366 | 0.242283 | intron-variant, utr-variant-3-prime | Wdr41, LOC105245591 | Mm_Celera | 13:95010758 | TGTCCCCAGAGTCAG[C/G]GTCTTCTCCTCTTTA | 218460 |
rs29250420 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr41 | Mm_Celera | 13:95004947 | GGTTGGGTGCAAATA[C/T]CTGCATCTGACTCTT | 218460 |
rs29774065 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr41 | Mm_Celera | 13:95004941 | TCCATTGGTTGGGTG[C/T]AAATACCTGCATCTG | 218460 |
rs30056119 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr41 | Mm_Celera | 13:95004936 | TTCTGTCCATTGGTT[A/G]GGTGCAAATACCTGC | 218460 |
rs30308144 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Wdr41 | Mm_Celera | 13:95000187 | AGACCCTGCTAAGGG[A/G]ACCCGGGCCTGGTGG | 218460 |
rs30308145 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Wdr41 | Mm_Celera | 13:95000166 | CGGGCCTGGCGGGCT[C/T]GCAGCAGACCCTGCT | 218460 |
rs30308146 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr41 | Mm_Celera | 13:95000136 | CTGTTGCTGCCGCAA[A/G]ACAAGTGAGCAGGTC | 218460 |
rs30308147 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr41 | Mm_Celera | 13:95000058 | ACACACCTACAGCCA[C/T]TTGAGTTTAAGACAA | 218460 |
rs30308148 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdr41 | Mm_Celera | 13:95000027 | TTCCTTAAGTTTTAC[A/G]AATCATTGTTTTCAC | 218460 |
rs30308149 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Wdr41 | Mm_Celera | 13:95000010 | AAATTAGATGAGATT[A/T]CTTCCTTAAGTTTTA | 218460 |
rs30308150 | snp | A/G | 0.124444 | 0.216185 | missense | Wdr41 | Mm_Celera | 13:94999878 | TAAGTTTGGGATTGC[A/G]ACACCGGCCGGCAAA | 218460 |
rs30308151 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr41 | Mm_Celera | 13:94999859 | CGATTTCTTAACATA[C/T]CTGTAAGTTTGGGAT | 218460 |
rs30308152 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr41 | Mm_Celera | 13:94999844 | AATTCTATTTGGCCA[C/T]GATTTCTTAACATAC | 218460 |
rs30308153 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr41 | Mm_Celera | 13:94999664 | GCATCTTTAAATGAC[C/T]TCACAGTGACACTGT | 218460 |
rs30309074 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr41 | Mm_Celera | 13:94999632 | AGATGAGCACTCTAG[A/G]GCACTCATTCTGGTG | 218460 |
rs30309075 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Wdr41 | Mm_Celera | 13:94999587 | TCCCACGAGGACACT[G/T]TAAGCAGGTTTGGTG | 218460 |
rs30309076 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr41 | Mm_Celera | 13:94999498 | CATTGGACTCTCAGA[A/G]GCTGTTGGGAGAGGT | 218460 |
rs30309077 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Wdr41 | Mm_Celera | 13:94999392 | CCTTACCACGTGGCA[A/G]GAGGCCGTTCCCGTG | 218460 |
rs30309078 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr41 | Mm_Celera | 13:94999088 | AAACAGGTGAATACA[C/T]AGGCACCTCCCTTTT | 218460 |
rs30309079 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr41 | Mm_Celera | 13:94999039 | GTCTCATAGCCAGAG[C/T]GCTTTTCTCTGAGTA | 218460 |
rs30309080 | snp | A/C/G | 0.277778 | 0.248452 | intron-variant | Wdr41 | GRCm38.p3 | 13:94998991 | GGAACGCAGAGTGGC[A/C/G]TTAGGACTGGGAGCT | 218460 |
rs30309081 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr41 | Mm_Celera | 13:94998966 | CTTTCACATAGTGAC[A/G]TCAGTGAAAGGAACG | 218460 |
rs30309082 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Wdr41 | Mm_Celera | 13:94998821 | CTTTGACATTCGTTT[A/T]ATCCAGATGGACTCT | 218460 |
rs30309083 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr41 | Mm_Celera | 13:94998800 | TTATTTTAAAAATCC[C/T]GAGAACTTTGACATT | 218460 |
rs30309934 | snp | A/T | 0.35503 | 0.226867 | intron-variant | Wdr41 | Mm_Celera | 13:94998791 | GAGTCATCCTTATTT[A/T]AAAAATCCCGAGAAC | 218460 |
rs30309935 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Wdr41 | Mm_Celera | 13:94998710 | AACTGCTGCTGCAGT[A/G]TGGAGGTGAGACGCT | 218460 |
rs30309936 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr41 | Mm_Celera | 13:94998652 | GTCTGTTTAAGCAGG[A/G]CTGTTTCTAGGATGC | 218460 |
rs30309937 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr41 | Mm_Celera | 13:94998491 | CTCTGTGTGCTGATG[C/T]AGGATTTGGTCAGAT | 218460 |
rs30309938 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Wdr41 | Mm_Celera | 13:94998469 | GACAACATTTAGACA[A/G]GCTACCCTCTGTGTG | 218460 |
rs30309939 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr41 | Mm_Celera | 13:94998057 | CAGTGTTAGACAAAT[C/T]GTCTGCAGGTAAGAA | 218460 |
rs30309940 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr41 | Mm_Celera | 13:94997977 | CCGGAGGAGGAATGG[A/G]TTCATAGACCTCCCT | 218460 |
rs30309941 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr41 | Mm_Celera | 13:94997964 | GTCAGAAATAAGCCC[A/G]GAGGAGGAATGGGTT | 218460 |
rs30309942 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr41 | Mm_Celera | 13:94997942 | GTCTGTCTGAGAGCT[A/G]AGTTAAGTCAGAAAT | 218460 |
rs30309943 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Wdr41 | Mm_Celera | 13:94997859 | CATCATTACAAGGAG[A/T]TGCATTGTGGGGCCA | 218460 |
rs30310734 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Wdr41 | Mm_Celera | 13:94997809 | AGCTGTGTACAGTGA[C/T]CTTCTGATAAAATAG | 218460 |
rs30310735 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Wdr41 | Mm_Celera | 13:94997807 | GAAGCTGTGTACAGT[G/T]ACCTTCTGATAAAAT | 218460 |
rs30310736 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr41 | Mm_Celera | 13:94997774 | GTTATGGAAGTAGGC[C/T]GAAATGGCCAGCAGC | 218460 |
rs30310737 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Wdr41 | Mm_Celera | 13:94997597 | CTTAAAGTGAGTTTG[C/G]CTTTGCCTCCCATAC | 218460 |
rs30310738 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Wdr41 | Mm_Celera | 13:94997568 | CAGTATCTCACACTT[C/T]GTATTATAAAAGTCT | 218460 |
rs30310739 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr41 | Mm_Celera | 13:94997457 | GAAAATAATCAATTT[C/T]GCCCTCGTGTATGAC | 218460 |
rs30310740 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr41 | Mm_Celera | 13:94997437 | AATGAGGATGAGTTG[A/G]ACTGGAAAATAATCA | 218460 |
rs30310741 | snp | A/C | 0.35503 | 0.226867 | intron-variant | Wdr41 | Mm_Celera | 13:94997387 | AAACGGCAGGGTGGA[A/C]GTGCGTGAGCTTAAA | 218460 |
rs30310742 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Wdr41 | Mm_Celera | 13:94997369 | TGTTACGTCAGGCTG[G/T]GCAAACGGCAGGGTG | 218460 |
rs30310743 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr41 | Mm_Celera | 13:94997198 | TCGGTATATCCTTAG[C/T]CTGAGACCCAGCAGC | 218460 |
rs30311494 | snp | G/T | 0.32 | 0.24 | synonymous-codon | Wdr41 | Mm_Celera | 13:94997169 | TCTCTTGACAGCCTC[G/T]GCTGACCGGACTGTC | 218460 |
rs30311495 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Wdr41 | Mm_Celera | 13:94997157 | CAGCAGTCAGCTTCT[C/T]TTGACAGCCTCGGCT | 218460 |
rs30311496 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Wdr41 | Mm_Celera | 13:94997045 | TGTTGACATTCCTAC[C/T]TGTGTTTCAGACAGG | 218460 |
rs30311497 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Wdr41 | Mm_Celera | 13:94996981 | ATATGTTTATTTTCT[A/C]CATAAGCTATTCTCA | 218460 |
rs30311498 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wdr41 | Mm_Celera | 13:94996898 | CAGCTGTTTTTAACA[C/T]TTATTTAGATTATAT | 218460 |
rs30311499 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr41 | Mm_Celera | 13:94996843 | ATGATGAAAATATCC[C/T]AAAATAGCATACTGA | 218460 |
rs30311500 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr41 | Mm_Celera | 13:94996700 | GCGCTGTCATTTCCA[C/T]TGCACCCAGAGCTGC | 218460 |
rs30311501 | snp | C/G | 0.32 | 0.24 | intron-variant | Wdr41 | Mm_Celera | 13:94996680 | AAGTGTGCCTGCAGA[C/G]CATGGCGCTGTCATT | 218460 |
rs30311502 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr41 | Mm_Celera | 13:94996515 | TCTATAAGTGGTGGA[C/T]GCAGAAGGCCAGCTG | 218460 |
rs30311503 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wdr41 | Mm_Celera | 13:94996343 | AAGATTGGTTGAATC[C/T]GGCCAGTCATCATGG | 218460 |
rs30312344 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Wdr41 | Mm_Celera | 13:94996304 | AACCACCATACATAT[G/T]AAAAAACACTGTAAT | 218460 |
rs30312345 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Wdr41 | Mm_Celera | 13:94996280 | TTCAGCATATTGAAG[A/T]CCAGGATAAACCACC | 218460 |
rs30312346 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr41 | Mm_Celera | 13:94996243 | CTGGCCCAGGTTGGC[C/T]CTGAACCTTTGTTCT | 218460 |
rs30312347 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr41 | Mm_Celera | 13:94996000 | ACAAGTGGCTCCAGT[C/T]CTCCTCAACCTCACA | 218460 |
rs30312348 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdr41 | Mm_Celera | 13:94995997 | TCCACAAGTGGCTCC[A/G]GTCCTCCTCAACCTC | 218460 |
rs30312349 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Wdr41 | Mm_Celera | 13:94995838 | TGGAGTTTCCTGGGG[C/T]GTCTCCTGGTGGTTT | 218460 |
rs30312350 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Wdr41 | Mm_Celera | 13:94995747 | GATAGCATAATAAAA[A/T]TTTCTCTCATGTTTG | 218460 |
rs30312351 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Wdr41 | Mm_Celera | 13:94995724 | CAGTTTTTCATTCAA[A/C]CTTGTATGATAGCAT | 218460 |
rs30312352 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Wdr41 | Mm_Celera | 13:94995682 | CAGTGACATCAGAAA[A/T]GAATTGTTAGTTTTT | 218460 |
rs30312353 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr41 | Mm_Celera | 13:94995381 | ACTGTGTGGTACTCA[A/G]TATGCTGGCTTATTA | 218460 |
rs30313034 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr41 | Mm_Celera | 13:94995338 | ATAATGAAAACATGG[C/T]ACTGTGGTTGAAAAC | 218460 |
rs30313035 | snp | G/T | 0.32 | 0.24 | intron-variant | Wdr41 | Mm_Celera | 13:94995241 | TCATGGTCTCTTTTC[G/T]CAAACCAGGTTTGCA | 218460 |
rs30313036 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Wdr41 | Mm_Celera | 13:94995182 | TATTACAATATTACA[C/T]TTAAAAAATCTCACC | 218460 |
rs30313037 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr41 | Mm_Celera | 13:94995156 | TTAATATGTATTTTC[C/T]CAAACAATTTTATTA | 218460 |
rs30313038 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Wdr41 | Mm_Celera | 13:94995111 | TAATGTAGCCTTAAT[A/C]ATTCATAATGTTACA | 218460 |
rs30313039 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Wdr41 | Mm_Celera | 13:94994307 | ACCCACACTCCACTG[C/T]GGTTATCTTTCCCCT | 218460 |
rs30313040 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Wdr41 | Mm_Celera | 13:94994203 | CTCCGAGACCACTCT[C/G]CACTCCAAAATTTCC | 218460 |
rs30313041 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdr41 | Mm_Celera | 13:94994175 | CACAAGTGCTGTCTA[C/T]GCCTCTCCAGAACTC | 218460 |
rs30313042 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdr41 | Mm_Celera | 13:94993520 | ATTTTTAAAAGTGTT[C/T]CTGGGGCTGGGAAGA | 218460 |
rs30313043 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr41 | Mm_Celera | 13:94993490 | TCAAGCATGAAACCC[A/G]AGTGGCCAGTGAGTA | 218460 |
rs30313794 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr41 | Mm_Celera | 13:94992826 | ATGGAATTTACAAGA[C/T]ATCTTATCAACATTT | 218460 |
rs30313795 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr41 | Mm_Celera | 13:94992623 | GTAAAATTCAATTCC[A/G]TCCCTAGACTGTTCC | 218460 |
rs30313796 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr41 | Mm_Celera | 13:94992458 | TTTTTGTGGCCTGAG[A/G]CAAACTGTTCTTTGT | 218460 |
rs30313797 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wdr41 | Mm_Celera | 13:94992447 | CTGCGGCTTCCTTTT[C/T]GTGGCCTGAGGCAAA | 218460 |
rs30313798 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Wdr41 | Mm_Celera | 13:94992376 | TCTATAATGTAGAAC[A/G]TATTCCTAGATTCAG | 218460 |
rs30313799 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Wdr41 | Mm_Celera | 13:94992138 | GTGGTGTGCTTCATT[A/T]TTAACAACAAGTCGA | 218460 |
rs30313800 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Wdr41 | Mm_Celera | 13:94992119 | CACTAGTGTTCATTA[C/T]AGAGTGGTGTGCTTC | 218460 |
rs30313801 | snp | C/G | 0.32 | 0.24 | intron-variant | Wdr41 | Mm_Celera | 13:94992005 | GAGCAGAGATGCATA[C/G]TTCACAGCTGGCTTT | 218460 |
rs30313802 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Wdr41 | Mm_Celera | 13:94991978 | CATCATTTATTAATG[G/T]TTGTTAACTGTGAGC | 218460 |
rs30313803 | snp | G/T | 0.32 | 0.24 | intron-variant | Wdr41 | Mm_Celera | 13:94991937 | GGAAGTAGCACAGAC[G/T]GAAAAATGATAGAAC | 218460 |
rs30314644 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Wdr41 | Mm_Celera | 13:94991887 | ACTGTACTGACTGAA[C/T]GGAGACTGTAAGGAA | 218460 |
rs30314645 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Wdr41 | Mm_Celera | 13:94991877 | CTTATGACCCACTGT[A/G]CTGACTGAATGGAGA | 218460 |
rs30314646 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Wdr41 | Mm_Celera | 13:94991709 | CTGATTAAACCTGGG[C/T]GTTTAATCAGCATGG | 218460 |
rs30314647 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr41 | Mm_Celera | 13:94991681 | AGCCTATGAAGACAG[C/T]AGGAGGCTGAAGCTG | 218460 |
rs30314648 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Wdr41 | Mm_Celera | 13:94991539 | AAACAGTGTAGATGG[G/T]GTTGACATGAACTAT | 218460 |
rs30314649 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Wdr41 | Mm_Celera | 13:94991472 | GGGCTTGGATGACTG[C/G]TTTCCATTACTCACC | 218460 |
rs30314650 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Wdr41 | Mm_Celera | 13:94991334 | GAAAAATTTGTCCTT[A/T]GAAAGTTTTATACAT | 218460 |
rs30314651 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr41 | Mm_Celera | 13:94991205 | TAAGGATTCACTTCC[A/G]GCAATTACCATTGAT | 218460 |
rs30314652 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Wdr41 | Mm_Celera | 13:94991152 | ACTGCTCTCTCTGTA[G/T]AAATACAAAGCAATC | 218460 |
rs30314653 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr41 | Mm_Celera | 13:94991131 | AAGGTTTTGAGTCCC[A/G]CCCTCACTGCTCTCT | 218460 |
rs30315474 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Wdr41 | Mm_Celera | 13:94991078 | TATAAGGGTTTGGAG[A/G]ATCAATAGAAATTGA | 218460 |