| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs3705669 | snp | G/T | 0.5 | 0 | intron-variant | Cfap57 | Mm_Celera | 4:118575189 | CACCTTGAGAAAATG[G/T]AAGGGAGAGTGGGGT | 68625 |
| rs3716416 | snp | C/G | 0.5 | 0 | intron-variant | Cfap57 | Mm_Celera | 4:118571862 | GGGAGTGAGACCTTG[C/G]TCCTTGACACTTGCC | 68625 |
| rs3717623 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cfap57 | Mm_Celera | 4:118572028 | TTCTAATTCAGTCGA[C/T]CTAGATCCCGGATTC | 68625 |
| rs3718421 | snp | A/C | 0.46281 | 0.131194 | intron-variant | Cfap57 | Mm_Celera | 4:118572201 | GAGGGACTGGAGTGG[A/C]ATGTGAGCATCTTCA | 68625 |
| rs3721268 | snp | A/G | 0.5 | 0 | intron-variant | Cfap57 | Mm_Celera | 4:118575385 | GCTATCAGCAAGCTC[A/G]ATCCAGAGCAGGGGA | 68625 |
| rs3721288 | snp | A/G | 0.5 | 0 | intron-variant | Cfap57 | Mm_Celera | 4:118575390 | CAGCAAGCTCAATCC[A/G]GAGCAGGGGAGGAAG | 68625 |
| rs3721809 | snp | A/G | 0.5 | 0 | intron-variant | Cfap57 | Mm_Celera | 4:118575441 | GAGGAGAGATGCACG[A/G]AGCCTTTGGGTTTTA | 68625 |
| rs3721868 | snp | A/T | 0.5 | 0 | intron-variant | Cfap57 | Mm_Celera | 4:118575468 | TTTATTCTAGTAGGA[A/T]GGGACACCACTGAGG | 68625 |
| rs3722579 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cfap57 | Mm_Celera | 4:118614389 | AGTTCTAATCAGCAC[C/T]GCTGGATCTAACCCG | 68625 |
| rs4140219 | snp | C/T | 0.5 | 0 | intron-variant | Cfap57 | Mm_Celera | 4:118575554 | GGTAGACGGGGCTGG[C/T]GAGACGGCTTGGCAG | 68625 |
| rs6166868 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Cfap57 | Mm_Celera | 4:118576747 | AGAAGGGGAAGGGAG[C/T]GATGTCACAAGGCCC | 68625 |
| rs6166977 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Cfap57 | Mm_Celera | 4:118576802 | TGAAAACACACAGTT[A/G]TGACGCCGCAGATGG | 68625 |
| rs6168074 | snp | C/T | 0.5 | 0 | intron-variant | Cfap57 | Mm_Celera | 4:118577016 | AGAAAAAGAAGTGGG[C/T]AGGATGATGTGCGGC | 68625 |
| rs6168580 | snp | A/G | 0.5 | 0 | intron-variant | Cfap57 | Mm_Celera | 4:118577059 | GTCTGCCTGCCTGAC[A/G]GTTCTGGGACACTTT | 68625 |
| rs6223295 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Cfap57, Ebna1bp2 | Mm_Celera | 4:118619058 | ctgcctctgcctcct[A/G]agtgctgggattaaa | 68625 |
| rs6393643 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Cfap57 | Mm_Celera | 4:118575093 | GAGCAAAGGCATTGC[C/T]GAGCATACCAGCACC | 68625 |
| rs13477940 | snp | A/G | 0.4352 | 0.167931 | intron-variant | Cfap57 | Mm_Celera | 4:118598524 | ATTGCCATTTGTTCC[A/G]TTTTTCTTGTGTTAC | 68625 |
| rs27495107 | snp | C/T | 0.260355 | 0.249785 | intron-variant, upstream-variant-2KB | Ebna1bp2, Cfap57 | Mm_Celera | 4:118622707 | TTAGCTTTTTAGAAA[C/T]GGAAGACTTGACGGA | 68625 |
| rs27495108 | snp | A/T | 0.46281 | 0.131194 | intron-variant, upstream-variant-2KB | Ebna1bp2, Cfap57 | Mm_Celera | 4:118622653 | GCAATGCCAAGGAGA[A/T]TACTGTTGCTTCTAG | 68625 |
| rs27495109 | snp | C/T | 0.152778 | 0.230321 | intron-variant, upstream-variant-2KB | Ebna1bp2, Cfap57 | GRCm38.p3 | 4:118622521 | TTAGCTTTTTAGAAA[C/T]GGAAGACTTGACGGA | 68625 |
| rs27495110 | snp | A/T | 0.42 | 0.183303 | intron-variant, upstream-variant-2KB | Ebna1bp2, Cfap57 | Mm_Celera | 4:118622467 | GCAATGCCAAGGAGA[A/T]TACTGTTGCTTCTAG | 68625 |
| rs27495111 | snp | A/G | 0.142012 | 0.225474 | upstream-variant-2KB, intron-variant | Cfap57, Ebna1bp2 | Mm_Celera | 4:118622375 | AAGTATGGGCCCTAC[A/G]AAAAGAAGCTTGCGT | 68625 |
| rs27495112 | snp | A/G | 0.244898 | 0.249948 | upstream-variant-2KB, intron-variant | Cfap57, Ebna1bp2 | Mm_Celera | 4:118622012 | AACTTCTGAGAGGCA[A/G]TAAGAAGACATGAGC | 68625 |
| rs27495113 | snp | C/T | 0.142012 | 0.225474 | upstream-variant-2KB, intron-variant | Cfap57, Ebna1bp2 | Mm_Celera | 4:118621731 | TAATTCATTTGAAGC[C/T]TGTGTGGGTGCCTCC | 68625 |
| rs27495114 | snp | A/C | 0.492188 | 0.0620098 | upstream-variant-2KB, intron-variant | Cfap57, Ebna1bp2 | Mm_Celera | 4:118621690 | TCACCGTTTAACCTG[A/C]ACCCTGCTCGAGGGA | 68625 |
| rs27495115 | snp | A/G | 0.497778 | 0.0332592 | upstream-variant-2KB, intron-variant | Cfap57, Ebna1bp2 | Mm_Celera | 4:118621677 | AATAGGTTCTTGGTC[A/G]CCGTTTAACCTGCAC | 68625 |
| rs27495116 | snp | A/G | 0.277778 | 0.248452 | upstream-variant-2KB, utr-variant-5-prime | Cfap57, Ebna1bp2 | Mm_Celera | 4:118620927 | GCGGGGCGGAAGGCC[A/G]CGAGATGGACACCCC | 68625 |
| rs27495117 | snp | A/C | 0.244898 | 0.249948 | upstream-variant-2KB, utr-variant-5-prime | Cfap57, Ebna1bp2 | Mm_Celera | 4:118620755 | CCGAAGCAATCCGGG[A/C]ACGCCCAAACGCTAG | 68625 |
| rs27495118 | snp | C/T | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Cfap57, Ebna1bp2 | Mm_Celera | 4:118620041 | ACGTGTGTTATTTTA[C/T]CTGTCATTTTGGCTA | 68625 |
| rs27495119 | snp | G/T | 0.260355 | 0.249785 | intron-variant, upstream-variant-2KB | Cfap57, Ebna1bp2 | Mm_Celera | 4:118618888 | TATTCTTGCAGAATA[G/T]TTACATGGTGTTTGA | 68625 |
| rs27495120 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Cfap57 | Mm_Celera | 4:118616667 | GGATGAATATGTTGT[C/T]CTGCAGCCCAACTCC | 68625 |
| rs27495121 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Cfap57 | Mm_Celera | 4:118616381 | GTCACATATTGGATG[A/G]TCGCACTAACATAGA | 68625 |
| rs27495122 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Cfap57 | Mm_Celera | 4:118615651 | CAACAAGCACGAAAT[G/T]CAAGCCACAGTGAAG | 68625 |
| rs27495123 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Cfap57 | Mm_Celera | 4:118615557 | TCCCGGAGACACACG[C/T]ATGCTGCCCCCCCAC | 68625 |
| rs27495124 | snp | C/T | 0.32 | 0.24 | intron-variant | Cfap57 | Mm_Celera | 4:118615415 | AGAACAGGGTCGAAT[C/T]GTACGGGCTTTAGTG | 68625 |
| rs27495125 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Cfap57 | Mm_Celera | 4:118615320 | ACAGAGAATGCAGAA[C/T]GGGGAGAGAATCCCA | 68625 |
| rs27495126 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Cfap57 | Mm_Celera | 4:118615171 | TAGTTTGACTGTATG[C/T]GGGTAATTGTAAAAT | 68625 |
| rs27495127 | snp | A/C | 0.415225 | 0.187619 | synonymous-codon | Cfap57 | Mm_Celera | 4:118614947 | GGCCGGTTTTTCTTG[A/C]ACAGTCTCGGAGATA | 68625 |
| rs27495128 | snp | A/G | 0.132653 | 0.220748 | synonymous-codon | Cfap57 | Mm_Celera | 4:118614869 | CTTTTGAACTTGGAA[A/G]TCAAAATTATTCAGG | 68625 |
| rs27495129 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Cfap57 | Mm_Celera | 4:118614348 | CCCAGGAGTTTACTG[A/C]AAAGCAGTCAGAACC | 68625 |
| rs27495130 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Cfap57 | Mm_Celera | 4:118613819 | AACTATGGCCTGGAG[A/G]AGACAGCCTTCCAGT | 68625 |
| rs27495131 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Cfap57 | Mm_Celera | 4:118613790 | AGAAGTGTTCTCCAC[C/T]CTGAGAGGCAGGAAA | 68625 |
| rs27495132 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Cfap57 | Mm_Celera | 4:118613778 | TGGGTCTACTGCAGA[A/G]GTGTTCTCCACTCTG | 68625 |
| rs27495133 | snp | C/T | 0.32 | 0.24 | intron-variant | Cfap57 | Mm_Celera | 4:118613510 | GTGAGTAGAGCTATA[C/T]TCTGTACCAGCATGA | 68625 |
| rs27495134 | snp | A/G | 0.32 | 0.24 | synonymous-codon | Cfap57 | Mm_Celera | 4:118613070 | GTCTTCAGACACCCA[A/G]GCGTGGGCTAGGTAG | 68625 |
| rs27495135 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Cfap57 | Mm_Celera | 4:118612932 | CTGTTACCTCTCTGA[C/T]TCTTGAATGACCTCC | 68625 |
| rs27495136 | snp | A/G | 0.32 | 0.24 | intron-variant | Cfap57 | Mm_Celera | 4:118612192 | CACCTCTGTGACCGT[A/G]TGGATGAAGTCAAGA | 68625 |
| rs27495137 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Cfap57 | Mm_Celera | 4:118612159 | TCTCGCAGGACATTT[C/T]GCTGTGTGAGCTGTG | 68625 |
| rs27495138 | snp | C/T | 0.32 | 0.24 | intron-variant | Cfap57 | Mm_Celera | 4:118611696 | GAGGCCTGGACCCAC[C/T]GAAATACTGTGCATA | 68625 |
| rs27495139 | snp | C/T | 0.32 | 0.24 | intron-variant | Cfap57 | Mm_Celera | 4:118611621 | TGAGAGCTGTTGGCC[C/T]TCTTCAGGAGAGGAG | 68625 |
| rs27495140 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Cfap57 | Mm_Celera | 4:118609930 | CTCAGGAAACTGTAT[C/T]TTTCTGGGTCCTGAG | 68625 |
| rs27495141 | snp | C/T | 0.32 | 0.24 | intron-variant | Cfap57 | Mm_Celera | 4:118609115 | TCATCTCTGGGTGTT[C/T]CCCGAGAACAATTCT | 68625 |
| rs27495142 | snp | C/T | 0.32 | 0.24 | intron-variant | Cfap57 | Mm_Celera | 4:118609019 | GCCCACTGCATCGGG[C/T]TTCTCCCCACACCCA | 68625 |
| rs27495143 | snp | C/T | 0.32 | 0.24 | intron-variant | Cfap57 | Mm_Celera | 4:118608688 | ACGCTTCCAGCTGCT[C/T]TTCTCTGCTCTGGCT | 68625 |
| rs27495144 | snp | C/G | 0.32 | 0.24 | intron-variant | Cfap57 | Mm_Celera | 4:118608581 | TCTACAGCTGGAACA[C/G]TAGCTATCCGGGGCA | 68625 |
| rs27495145 | snp | C/T | 0.32 | 0.24 | intron-variant | Cfap57 | Mm_Celera | 4:118607696 | CTGCCAGCGAGCCTT[C/T]CCTGAGCGTCCTGGG | 68625 |
| rs27495146 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Cfap57 | Mm_Celera | 4:118607227 | TTTCTGCATACTTGC[C/T]GTCTGCTTTGGCCTC | 68625 |
| rs27495147 | snp | G/T | 0.495868 | 0.0452663 | intron-variant | Cfap57 | Mm_Celera | 4:118607198 | GATGCGGATGGGCTG[G/T]CCTGCACACACCATT | 68625 |
| rs27495148 | snp | C/T | 0.32 | 0.24 | intron-variant | Cfap57 | Mm_Celera | 4:118606740 | AGGGTCCCACATGGT[C/T]GGTCAGCATGTCCCT | 68625 |
| rs27495149 | snp | C/T | 0.32 | 0.24 | intron-variant | Cfap57 | Mm_Celera | 4:118606282 | GATGGTAGTAGATTC[C/T]GTTCCCTGAGACACC | 68625 |
| rs27495150 | snp | A/G | 0.32 | 0.24 | intron-variant | Cfap57 | Mm_Celera | 4:118606188 | GAGTGTTTTATGGTG[A/G]TCTCCTTTGCAATTC | 68625 |
| rs27495151 | snp | C/T | 0.32 | 0.24 | intron-variant | Cfap57 | Mm_Celera | 4:118606113 | CAGGGGGCACAGGTC[C/T]GAAACATCTCTTATT | 68625 |
| rs27495152 | snp | C/T | 0.32 | 0.24 | intron-variant | Cfap57 | Mm_Celera | 4:118602617 | AATGTCCATGATACC[C/T]GACTCATACATAAAT | 68625 |
| rs27495153 | snp | C/T | 0.32 | 0.24 | intron-variant | Cfap57 | Mm_Celera | 4:118602519 | GTCAGGGAGCCAGTC[C/T]AGCAAGCTCACTGGT | 68625 |
| rs27495154 | snp | C/T | 0.32 | 0.24 | intron-variant | Cfap57 | Mm_Celera | 4:118602392 | TCCTACGTTTATGTC[C/T]ACCCACCTCCTGCTT | 68625 |
| rs27495155 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Cfap57 | Mm_Celera | 4:118602362 | TGAAGCCAAGACAAA[A/G]GCTGAGATGAGGACT | 68625 |
| rs27495156 | snp | A/T | 0.32 | 0.24 | intron-variant | Cfap57 | GRCm38.p3 | 4:118601377 | AAGAGGATACAGGGG[A/T]CAGATCTGGGAGGAA | 68625 |
| rs27495157 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Cfap57 | Mm_Celera | 4:118601028 | ATGGTTTTCCTGATG[C/T]GGTGTGATTTCAAAA | 68625 |
| rs27495158 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Cfap57 | Mm_Celera | 4:118601008 | AAACTGTTTCAATGT[C/T]ACACATGGTTTTCCT | 68625 |
| rs27495159 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Cfap57 | Mm_Celera | 4:118600971 | CTTTATTAGCCTGTG[C/T]ATACAGAACTCACGC | 68625 |
| rs27495160 | snp | G/T | 0.375 | 0.216506 | intron-variant | Cfap57 | Mm_Celera | 4:118600957 | TAGTACCTGGGACCC[G/T]TTATTAGCCTGTGTA | 68625 |
| rs27495161 | snp | A/G | 0.48 | 0.0979796 | synonymous-codon | Cfap57 | Mm_Celera | 4:118600864 | GTACTCGAAGTGGGC[A/G]GCCTCTCCCTGGGGA | 68625 |
| rs27495162 | snp | A/G/T | 0.444444 | 0.157135 | intron-variant | Cfap57 | GRCm38.p3 | 4:118600697 | AGCGGCCGACTTTCC[A/G/T]TACGCATGATAGCAG | 68625 |
| rs27495163 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Cfap57 | Mm_Celera | 4:118600637 | GAAAGCGTCTAGGTC[A/G]TTCGATTGTAAACCT | 68625 |
| rs27495164 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Cfap57 | Mm_Celera | 4:118600625 | GCTTTTCCAGCTGAA[A/T]GCGTCTAGGTCATTC | 68625 |
| rs27495165 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Cfap57 | Mm_Celera | 4:118600570 | TTTTAGCCCATGCAA[A/G]ACTGAGAGGCTGCTG | 68625 |
| rs27495166 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cfap57 | Mm_Celera | 4:118600557 | CCAGAAAGTAATTTT[C/T]TAGCCCATGCAAAAC | 68625 |
| rs27495167 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Cfap57 | Mm_Celera | 4:118600325 | CCAGAAGAATATAAC[C/T]GATGGGGAGCCAAGG | 68625 |
| rs27510768 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Cfap57 | Mm_Celera | 4:118599785 | TGATGTTTTAAGTCA[C/T]CAGGGCCCCAGAAGA | 68625 |
| rs27510769 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cfap57 | Mm_Celera | 4:118599762 | AGTCTGGTGACAGAT[A/G]CACTGGCTGATGTTT | 68625 |
| rs27510770 | snp | C/T | 0.5 | 0 | intron-variant | Cfap57 | Mm_Celera | 4:118598841 | CTAAATTAAGCCCAC[C/T]TCTTCAGCAGACTGC | 68625 |
| rs27510771 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | Cfap57 | Mm_Celera | 4:118598775 | CAGCTCTGTCTGCGT[G/T]CGTAACTTCTGACCA | 68625 |
| rs27510772 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Cfap57 | Mm_Celera | 4:118598736 | TGTGGGGTTTGCCTT[C/T]TCACATGTAATGGTC | 68625 |
| rs27510773 | snp | A/G | 0.32 | 0.24 | intron-variant | Cfap57 | Mm_Celera | 4:118598727 | TGATCGATCTGTGGG[A/G]TTTGCCTTTTCACAT | 68625 |
| rs27510774 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Cfap57 | Mm_Celera | 4:118598705 | TCATTACCTCTGACA[A/C]GTCCTGTGATCGATC | 68625 |
| rs27510775 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cfap57 | Mm_Celera | 4:118598656 | AGTTCACCTGTGTGC[C/T]GCCTGACACCTATGT | 68625 |
| rs27510776 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Cfap57 | Mm_Celera | 4:118597773 | GGTCCAAGCATGTTC[G/T]TATTTAGCCTGTTAA | 68625 |
| rs27510777 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Cfap57 | Mm_Celera | 4:118597750 | GAGCTCAGTCTGGGA[A/G]TTCTTGAGGTCCAAG | 68625 |
| rs27510778 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Cfap57 | Mm_Celera | 4:118597713 | AATAGGAATGAACAG[A/G]CCAATGCGTAACATT | 68625 |
| rs27510779 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Cfap57 | Mm_Celera | 4:118597606 | AGAAGAAGAGAATTG[A/G]TCTCGTCAGATCTAT | 68625 |
| rs27510780 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Cfap57 | Mm_Celera | 4:118597596 | CCAGCATGATAGAAG[A/G]AGAGAATTGGTCTCG | 68625 |
| rs27510781 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cfap57 | Mm_Celera | 4:118597501 | TTATGCCATGAAAAT[A/G]AAATATAGGCCCAGT | 68625 |
| rs27510782 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Cfap57 | Mm_Celera | 4:118597466 | TAATGAAAAGAAAAT[A/T]CAGAGCTGGTGAGTT | 68625 |
| rs27510783 | snp | A/C | 0.32 | 0.24 | intron-variant | Cfap57 | Mm_Celera | 4:118596164 | AATGCAGCTTCCTGG[A/C]CACATTAACATGCTG | 68625 |
| rs27510784 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Cfap57 | Mm_Celera | 4:118596013 | GAGTATACAGGCATG[C/T]ACACGCACAAGCGCG | 68625 |
| rs27510785 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Cfap57 | Mm_Celera | 4:118595975 | ACGGATCTGCAAGGG[A/G]TGCAGGCATACCTGG | 68625 |
| rs27510786 | snp | A/C | 0.336735 | 0.234472 | missense, intron-variant | Cfap57 | Mm_Celera | 4:118595833 | GGGAGGTGGTGACCG[A/C]GTTGTAGCTACAGGA | 68625 |
| rs27510787 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Cfap57 | Mm_Celera | 4:118595706 | AGCCCAGGAGCCTGT[C/T]TTCTGTAGCACTGAG | 68625 |
| rs27510788 | snp | A/G | 0.32 | 0.24 | intron-variant | Cfap57 | Mm_Celera | 4:118595637 | GTGAGCTGGCATGAC[A/G]CAGTAGAGAACCCAG | 68625 |
| rs27510789 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Cfap57 | Mm_Celera | 4:118595605 | CAGTTTGATCCATTC[A/G]GGGGCATCAAAGAGT | 68625 |