| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs245047454 | in-del | -/AC | | | intron-variant | Yaf2 | Mm_Celera | 15:93327171 | GATAGATGTTTGTGA[-/AC]CACCATTTGTGTTGC | 67057 |
| rs245115782 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93331979 | AGGGCCCTTGTTTTG[C/T]CTCTCTTATTTCTAT | 67057 |
| rs245180937 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Yaf2 | Mm_Celera | 15:93284924 | AGGTGCATTAAGAGG[A/G]TAACCATTAAGAAAA | 67057 |
| rs245218082 | snp | A/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93324047 | TGCAGACAGGCAGGG[A/T]GGAGCTCCATTAAGA | 67057 |
| rs245223011 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93294023 | CACATAAGCACATCT[A/C]TTGCCTAAGTAGAAC | 67057 |
| rs245241501 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93312694 | GCAAACAACAACCAA[A/G]ACAAAACAACCTTAT | 67057 |
| rs245248858 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93323592 | GTGGTTCTAAACATA[C/T]ATGCTATTGATAGTG | 67057 |
| rs245279478 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93332896 | ATTCAATCATCAGCA[A/G]TTACTACCTTCACAG | 67057 |
| rs245302543 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93287410 | ATCAGTCAGACAAGG[C/T]CCCTCCAGCTTCACA | 67057 |
| rs245323816 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93325047 | ATCTCCAAAGGAAGT[C/T]AGGACAGGAACTCAA | 67057 |
| rs245513202 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93315791 | ATGGAGAAGACAGAG[A/G]GTGGATTGGGGGGGT | 67057 |
| rs245529806 | in-del | -/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93289709 | GCACAGCTGGGCGCG[-/C]CTCCCCTGGGAGCTG | 67057 |
| rs245531019 | in-del | -/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93303252 | TTAAAATTTACTTTG[-/T]TATCTGAGTGTTTAG | 67057 |
| rs245556870 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93335069 | GCTCATTTACAAATA[A/C]ACATATATTATACAC | 67057 |
| rs245677981 | snp | G/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93306700 | AACCATGCTGGGCAC[G/T]GTGGCGCACACCTTT | 67057 |
| rs245706867 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93294784 | AATTTTAGAGTCAGA[A/G]GGAATGGATGGCACC | 67057 |
| rs245751734 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93331669 | CGTTTACCTCCCCAC[A/G]CCTCTGCACCTCACA | 67057 |
| rs245807573 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93295535 | TGTTTGTCTTCTCCA[C/T]CCTACTGTAACCTGG | 67057 |
| rs245840728 | in-del | -/TTTAAT | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93306025 | TCCTTAGCTTTTAAC[-/TTTAAT]TTTAATTTTTTTCCC | 67057 |
| rs245846103 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93302667 | GCAGATTCCTGTGAG[C/T]CTGAGGCCAGCCTGT | 67057 |
| rs245853781 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93319337 | CTCCGCCTCCCAAGC[A/G]CCTGAATTTAAAGCG | 67057 |
| rs245885735 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93318714 | TGGCACAAATAGCAA[A/G]GTCTCTTAGAGTAGC | 67057 |
| rs245920130 | snp | G/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93300245 | GCCCCAGGCTGCTCT[G/T]CTGCTCTCACTCCTG | 67057 |
| rs246065844 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93287515 | TTGGATATACACACA[C/T]GCATGCGCACGCGCG | 67057 |
| rs246083076 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93301850 | GAGGACGTCCCTGGC[C/T]GAGGAAGGACGGGGC | 67057 |
| rs246162865 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93299300 | CACAAAAGCCAAGTA[A/G]TTGTGGCAAGTGCCT | 67057 |
| rs246191835 | snp | C/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93327692 | AGGAAAGTAGCAGAG[C/G]AGGCCGGAGGGGGCC | 67057 |
| rs246209076 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93298566 | CTGGCCAGAATACAA[A/C]AGTGCATCTGAGACA | 67057 |
| rs246217622 | in-del | -/TAAAC | | | utr-variant-3-prime, nc-transcript-variant | Yaf2 | Mm_Celera | 15:93283921 | TTTTACTGTATGCAA[-/TAAAC]TATTCACAACTAGCA | 67057 |
| rs246287640 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93320530 | CAGTCAACATAAGAA[C/T]CTGGGTAGGATAAAG | 67057 |
| rs246304741 | in-del | -/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93297458 | TGAGAAGCGGGACAG[-/T]TAAAGAAGAGGAAGC | 67057 |
| rs246322459 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93319791 | GAAGCAAGACCTCAC[A/G]CATTAGCCAATGTTC | 67057 |
| rs246332513 | snp | G/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93307736 | CCAACTGAGGATAAC[G/T]AAGAAGTGCAAGGTG | 67057 |
| rs246346045 | in-del | -/CCTG | | | intron-variant | Yaf2 | Mm_Celera | 15:93289557 | AAATTCTATGTAAGT[-/CCTG]CCTGGCCTTTTCTCA | 67057 |
| rs246354483 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93328392 | GAGAAAGATAGTACG[A/G]AGGGTGATGAAGAAT | 67057 |
| rs246426391 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93299589 | GCTTGTTGTTTCATG[A/G]AGCAGTTTGTGTATA | 67057 |
| rs246486023 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93326159 | AACGCAAACAGTAAA[A/G]ACCTCATTCTAAGCA | 67057 |
| rs246510390 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93334148 | TTCCATCCTATCTGC[C/T]AACAGGCACATCAAC | 67057 |
| rs246526125 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93300189 | TCTTCGACCCAGCCC[C/T]GCTTGGATGCTCTGT | 67057 |
| rs246583279 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93333571 | ATGTGTGTACATACA[C/T]GCATGTAAGTATACA | 67057 |
| rs246637467 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93326357 | CCTCTTAGGGTACCA[A/C]GCAATCCTAACCAGT | 67057 |
| rs246644813 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93306912 | TTACAGACTAAAATA[C/T]TACATGTCAGTGTTT | 67057 |
| rs246671922 | in-del | -/AAAAACAAAAAC | | | intron-variant | Yaf2 | Mm_Celera | 15:93334677 | TTGGATCTACTGGTT[-/AAAAACAAAAAC]AAAAACAAAAACAAA | 67057 |
| rs246678866 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93325581 | AGCTGGGAATGTGCG[A/C]ATGCGGAGGCCTTTA | 67057 |
| rs246681323 | in-del | -/A | | | intron-variant | Yaf2 | Mm_Celera | 15:93292221 | TGGGGGCATCTAGGG[-/A]AGACAACAGTGGCCT | 67057 |
| rs246719662 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93306134 | TTATTATTATTATTA[C/T]TATTATTTATTTATT | 67057 |
| rs246789396 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93299008 | CTAGTTGACTAAACA[C/T]CTTCCATGCTTCACT | 67057 |
| rs246824427 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93334562 | TTAGGAACACGGTGT[C/T]CCTTAGACTTCTGGT | 67057 |
| rs246854026 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93293773 | GTGTGATCTCTCTTC[A/C]ATTTGATAAGAGCAA | 67057 |
| rs246860890 | in-del | -/TTC | | | intron-variant | Yaf2 | Mm_Celera | 15:93315226 | CTGACCCATAATTGT[-/TTC]TGTCTGAAAGAATTA | 67057 |
| rs246902793 | snp | G/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93335678 | TAACTCTTTTAAATG[G/T]TTTTTTTTTTTTTTT | 67057 |
| rs247028648 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93327475 | CAAAAGCGCAGTTCC[A/C]GAGGCCCTAGAGCTA | 67057 |
| rs247054446 | snp | A/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93328308 | CTGAATGGGCTTTGG[A/T]GCTAGGACATGGAGA | 67057 |
| rs247080213 | snp | C/T | | | upstream-variant-2KB | Yaf2 | Mm_Celera | 15:93337525 | CGGGTACCCCACAAC[C/T]AGAGTTAGCTTGACA | 67057 |
| rs247126697 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93318686 | TTAATACTGTTATGA[A/C]GTATCTAGTACATGG | 67057 |
| rs247130330 | snp | A/G | | | upstream-variant-2KB | Yaf2 | Mm_Celera | 15:93338550 | CTCTCTTATAAGGAC[A/G]TCACTCATTGGATTA | 67057 |
| rs247294569 | snp | A/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93295180 | GAGAGAGAGAGAGAG[A/T]GTTAAACAAGAGAGA | 67057 |
| rs247337242 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93300780 | TGTAGCCCTAATTCT[A/G]CTTAGAGTAACTTCA | 67057 |
| rs247359252 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93296412 | TTTAGGCTGTAACTG[C/T]TTCTATGGTCTTAAG | 67057 |
| rs247379965 | snp | C/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93318471 | CCTAGGGCTAAGCAA[C/G]CCCCGGCCACCTGAG | 67057 |
| rs247454320 | in-del | -/ACTT | | | intron-variant | Yaf2 | Mm_Celera | 15:93300328 | TGTTTCTATTAACTC[-/ACTT]AGTCTCCACGGCAAC | 67057 |
| rs247462883 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93285931 | CTGACTCCAGGGGCA[A/G]CAGATGTGACACCAT | 67057 |
| rs247474359 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93326179 | CATTCTAAGCACGGC[C/T]TCTTAGAGCTTTACG | 67057 |
| rs247531024 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93289633 | TTGGAATAAGCTGCG[A/G]AGCAATGAGAAGAAG | 67057 |
| rs247541798 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93297513 | CATGCCCAAAGATTC[A/G]CAGAATTTACAAAGC | 67057 |
| rs247651959 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93297872 | AGGTGTGCACCACCA[C/T]GCCCGGCTACATATA | 67057 |
| rs247759108 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93302854 | GGCGAAACTACAGAA[A/C]GGCAGCAAGCGTGAG | 67057 |
| rs247832184 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93295345 | AACCGGTGCTCCTGT[C/T]GCTACCCTAGGTTTC | 67057 |
| rs247939542 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93307622 | ACTTGGGAAGCATGA[A/G]GCCATATATTTCTGA | 67057 |
| rs247974799 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93319074 | CCACCACAGGGACTG[C/T]GCTCTTTCCAGAAGC | 67057 |
| rs247982094 | snp | A/G | | | upstream-variant-2KB | Yaf2 | Mm_Celera | 15:93337107 | CCCCGGAGCGCTCCG[A/G]CCGTGGCTCGCACGC | 67057 |
| rs247982416 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93288015 | AAAAAATAGCAGGAT[A/G]CAACCAAAAGATGAG | 67057 |
| rs248032044 | in-del | -/A | | | intron-variant | Yaf2 | Mm_Celera | 15:93292494 | AACAAAACCAGATTT[-/A]AAAAAAACAAAACCA | 67057 |
| rs248122710 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93290918 | TCAAAAATACAAAGT[A/G]TAGCTAAGAAACTGT | 67057 |
| rs248143711 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93301014 | CCTTGATTTTTGTGG[A/G]TAATGTCTCTTAGAA | 67057 |
| rs248183060 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93287140 | ACATCACAGGCCCCT[A/G]GACTTCCTCCCAAGA | 67057 |
| rs248229945 | snp | C/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93322115 | CTGATCTCCACAGCT[C/G]AAGTCTTAGGTGGTT | 67057 |
| rs248293187 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93317774 | CTAAACATTTACTCA[C/T]CAAAAGAAAAATGGA | 67057 |
| rs248346347 | snp | A/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93310872 | CGATATATTTTGAAA[A/T]TTAAATTTTCTACAA | 67057 |
| rs248372543 | in-del | -/A | | | intron-variant | Yaf2 | Mm_Celera | 15:93287600 | GGAAATCCTATCCTG[-/A]AAAAAAAAAAAAAAA | 67057 |
| rs248377381 | in-del | -/CG | | | intron-variant | Yaf2 | Mm_Celera | 15:93287534 | GCGCACGCGCGCACA[-/CG]CACGCACACGCACAC | 67057 |
| rs248415037 | snp | A/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93308083 | AGAATCCCCTGGGTC[A/T]ATGACAGCCAGTGTG | 67057 |
| rs248424795 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93328635 | GCGACGTCACTGCTG[C/T]CTGTTTTGCTAATGG | 67057 |
| rs248438440 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93313686 | CTGCAGCTGTTAATA[C/T]TGCCTAGCAAGTCTG | 67057 |
| rs248525752 | in-del | -/CC | | | intron-variant | Yaf2 | Mm_Celera | 15:93300439 | TATATACCAAATCAT[-/CC]TGTGAAAATCTTTAA | 67057 |
| rs248548237 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93308340 | AGCCTAGAGTTGATC[A/G]ACTCCAAAGACATTT | 67057 |
| rs248551977 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93331028 | CTGCATTGATTATCA[A/G]GAAATAACAGCTCAC | 67057 |
| rs248611142 | snp | A/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93329451 | AATGGCACGGGATTG[A/T]GAACTGTAACTAGAG | 67057 |
| rs248699751 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93301546 | GGGGATGACACTTGT[A/G]GACCACACCGAGTTT | 67057 |
| rs248709250 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93301248 | CTGTAATGAAGCTGA[C/T]GCTTTCATTTTCCTG | 67057 |
| rs248753130 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93316315 | GAAATAAGTGCAGCA[A/C]CCCCAAGAGCATGCT | 67057 |
| rs248776997 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93296909 | TGTTTGTGTGTATGT[A/G]TGTGCATGCCATGGA | 67057 |
| rs248808883 | snp | A/G | | | upstream-variant-2KB | Yaf2 | Mm_Celera | 15:93337860 | TACTCAGAGTGAGAT[A/G]GCAACTAAAAACTTG | 67057 |
| rs248818846 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93296275 | TCTAAGTGGGAGAGG[A/G]AGACACAGCAGGAAG | 67057 |
| rs248829790 | in-del | -/AAAAAAAAA | | | intron-variant | Yaf2 | Mm_Celera | 15:93296192 | AAGGCAATTTGCTGC[-/AAAAAAAAA]AAAAAAAAAAAAAAT | 67057 |
| rs248833685 | in-del | -/A | | | intron-variant | Yaf2 | Mm_Celera | 15:93292379 | GACAATGAGACCTTT[-/A]AAAAAAAAGTGGACT | 67057 |
| rs248879439 | snp | A/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93296210 | AAAAAAAAAAAAAAA[A/T]AAAATTGTGACCCTG | 67057 |
| rs249005273 | in-del | -/GG | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93295087 | TTGTTTCATTTTGGT[-/GG]GGGGGGGGGTTCTGT | 67057 |
| rs249022855 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93300439 | TATATACCAAATCAT[C/T]CTGTGAAAATCTTTA | 67057 |
| rs249042857 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93304028 | CTGATCACCTAGGTC[A/G]CAGAGGAGGAGAGAT | 67057 |
| rs249270159 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93311076 | GTCCTGGAACTCACT[C/T]TGTAGACCAGGATGG | 67057 |
| rs249328087 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93329444 | GGAAAGAAATGGCAC[A/G]GGATTGTGAACTGTA | 67057 |
| rs249469308 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93321453 | TATTAAACAATGGCA[A/C]ATTTTTCTAGTGTGA | 67057 |
| rs249554835 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93323518 | TTCTCCTAAATGGTC[C/T]TCTGCAGTTAGAATT | 67057 |
| rs249651867 | in-del | -/CAA | | | intron-variant | Yaf2 | Mm_Celera | 15:93313572 | CTGTAAAGAAAACAC[-/CAA]CAAGCCCACTCCTCC | 67057 |
| rs249664611 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93288820 | CTCAAAGTCCAATGT[A/C]CTGGACCTATGAGTT | 67057 |
| rs249720555 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93319142 | TTTCTTCCTCCAGTA[C/T]CCACCTTCATGGATT | 67057 |
| rs249781902 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93290576 | CCAAGAATGAATGTA[A/G]AGGAATGAATAATAA | 67057 |
| rs249831475 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93289558 | AAATTCTATGTAAGT[C/T]CTGGCCTTTTCTCAA | 67057 |
| rs249845479 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93331906 | GAACAAGCACGACTG[A/C]TCTTCACGTAGTGGA | 67057 |
| rs249889318 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93322953 | CACTGTCCATTCTCC[A/G]CGGCTTCTCCCTCCT | 67057 |
| rs249955980 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93297050 | GGGCTGTCTCTCTGG[C/T]CCTAGGTTATAATAT | 67057 |
| rs249991647 | snp | G/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93287364 | GTGCCTTCTTGGCTT[G/T]GCCTTTAATGCTGGC | 67057 |
| rs250030774 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93290664 | AACCAGCCAGATCCA[A/G]TGCACATCATCTCTG | 67057 |
| rs250043102 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93324619 | AGGGTAGAAACTGAC[C/T]TTAGCAATTTACGAA | 67057 |
| rs250085174 | snp | A/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93327087 | ACTGCTTACTACTTA[A/T]GCTACGTGTTCTGCC | 67057 |
| rs250093830 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93312065 | GCCTGGGTCCCACAA[C/T]CCGTGTATCAACCTA | 67057 |
| rs250121752 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93290287 | ACTGCAGAGGACACA[C/T]GTTCAGGAATAAGAG | 67057 |
| rs250222796 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93292005 | AATAAAATAGTTGAG[A/G]ATACTATAGTTAGTC | 67057 |
| rs250330155 | in-del | -/CACACG | | | intron-variant | Yaf2 | Mm_Celera | 15:93287533 | ATGCGCACGCGCGCA[-/CACACG]CACACGCACACACGG | 67057 |
| rs250331378 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93331231 | GGGTTTGTAAAAGTA[C/T]AGTTTTCACTTGACT | 67057 |
| rs250333790 | snp | C/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93321343 | TCAAACCCTGGTCCT[C/G]TCTAAGAGCAACAAG | 67057 |
| rs250355532 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93313537 | TAAGTCTAAGGTACC[A/G]AGCACACGTCAACTC | 67057 |
| rs250386908 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93310852 | CTGGCCAACACACGC[A/G]TTAACGATATATTTT | 67057 |
| rs250392237 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93323690 | TGGGGGAAAATGTAC[C/T]CCATGTAACTCAAAA | 67057 |
| rs250393546 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93312492 | GAGAATTACCTAGGT[A/G]AACTCCAGAATACAA | 67057 |
| rs250533486 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93332433 | CCCTCACTTATAAAA[C/T]TGTATTTATGCCAAA | 67057 |
| rs250635628 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93288976 | GCCTTCCCTCCCTTC[C/T]GCCCCAGAGATGGCC | 67057 |
| rs250684510 | snp | C/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93295910 | GGTCAAGCCTGCAGA[C/G]CAGTGCAGCCTCACT | 67057 |
| rs250735023 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93290358 | TTAACAAAGACTATG[A/G]TACATAGTCTTTGTT | 67057 |
| rs250911088 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93321854 | TTTGCCTGTTTTATT[C/T]AAGGTCTGGGTTCAA | 67057 |
| rs250946172 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93321110 | ACAAATAATGGTCAC[A/C]ATATTTAAATTGCTT | 67057 |
| rs251018477 | snp | C/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93310762 | AGTCCAGGGCTGGCA[C/G]CACCCACAATAGTCA | 67057 |
| rs251029186 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93297968 | CAAGGACACTGGGGA[C/T]AGACCCTACACTAGA | 67057 |
| rs251107294 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93328218 | AAAAAATTCTGCATG[A/G]AGGGACACTGCATGG | 67057 |
| rs251110178 | snp | C/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93322881 | ATGTGGTAAATGAGT[C/G]TTACATATGTATGTA | 67057 |
| rs251113319 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93303661 | ACTTTAAAGCAGCGG[A/G]CGGTAAGCCAGCTAA | 67057 |
| rs251124767 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93289441 | TGGTGTCTGAAGACA[A/G]CTACGTGTACTCATT | 67057 |
| rs251134540 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93331386 | TCAAGTGTAAACGAC[A/G]TTTCATGAAAATGAA | 67057 |
| rs251138048 | snp | G/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93310364 | GTGATGAAACACCAT[G/T]GCCAGAGGAATCTGG | 67057 |
| rs251159210 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93305865 | TGAAGTGCTGCTTCC[A/G]GCACACACAGACTTA | 67057 |
| rs251225590 | snp | G/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93328795 | CCAACAAGCTTCATT[G/T]TATACGGTCAGTGAC | 67057 |
| rs251334281 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93299123 | CAGGATATCTGCTTC[C/T]GGCAACTCTAGTCAC | 67057 |
| rs251417591 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93332921 | TCACAGGCAACACTA[C/T]ATACATCCCTTTCTA | 67057 |
| rs251611577 | snp | C/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93325775 | GCCCAAAAAAGAGAT[C/G]ATGCTTTATCTAAAA | 67057 |
| rs251618598 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93305632 | CAACAGAACTGGGGA[A/G]GCGGCTCAGTCAGTA | 67057 |
| rs251640912 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93291520 | TTCTGGTGTGTCTGA[A/G]GACAGCTACAGTGTA | 67057 |
| rs251701151 | in-del | -/TTA | | | intron-variant | Yaf2 | Mm_Celera | 15:93316748 | GATAAATAAATCTTT[-/TTA]AAAAAAAAAAAATGC | 67057 |
| rs251731280 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | Yaf2 | Mm_Celera | 15:93284152 | CCCATAGGCAGATAT[A/T]TATTAAGCAAATGGC | 67057 |
| rs251767528 | snp | A/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93326101 | CCATCACCACCAACA[A/T]ATCAGAGTAGAGCCT | 67057 |
| rs251814426 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93312590 | ATTCAGGAGACAGAG[A/G]CAGGGAGGTAGGTCT | 67057 |
| rs251834053 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93292100 | AAACAAGTGACATTA[C/T]ATCTATACTAGGGTC | 67057 |
| rs251893192 | snp | A/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93293942 | GGTTGCTTCAGAATT[A/T]GGCACGATCACTCTG | 67057 |
| rs251903014 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93334351 | CTACTTATTAACAAG[A/G]CCATGTTCTACTGAT | 67057 |
| rs251937565 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93323161 | GCCAACCATTACAAT[A/G]GACTGATGGCCCCTC | 67057 |
| rs251941505 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93314367 | CTACAATGGAAGCAC[C/T]CAGAACTAATTACAG | 67057 |
| rs251956636 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93293080 | CTTAACAGTCAGTCA[C/T]GGAGGGGAAAGGGGC | 67057 |
| rs251960790 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93299613 | GTGTATACTATAACT[A/G]CAAGCTGACAAGGAA | 67057 |
| rs252111638 | snp | A/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93317006 | ACTCTGCCGAAATAA[A/T]CTGACCAAATTTGTA | 67057 |
| rs252111703 | snp | G/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93306460 | AGAACACAGGCAGAT[G/T]TATAACTCTAATTCA | 67057 |
| rs252144010 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93315650 | ACTGCCAGGTCTGTG[C/T]TCATTCAGAAATGAC | 67057 |
| rs252183997 | snp | G/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93318840 | TGAATGATTTCAATT[G/T]TAAGTGACTAGTTCA | 67057 |
| rs252214799 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93326788 | AGCAGAGTCTTGGCT[A/C]GCTCTCTCGTCTGAG | 67057 |
| rs252220910 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93317802 | GGATAAAAATGTGAC[C/T]GACATAGTCAGAAAT | 67057 |
| rs252328906 | snp | C/G | | | synonymous-codon, nc-transcript-variant | Yaf2 | Mm_Celera | 15:93285574 | TAGATCTCCAACAGT[C/G]ACTTCCAAATGCTGA | 67057 |
| rs252420366 | snp | A/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93316811 | ACTTGCTGTGTCCAA[A/T]GCTAAGAAAGAAAGG | 67057 |
| rs252483754 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93333717 | CACATACACGTATGT[A/G]TGTATACAGTACATG | 67057 |
| rs252490970 | snp | C/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93297622 | ACTCGGGCTGTGGGA[C/G]GCTCGACCTGACAGA | 67057 |
| rs252531333 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93305335 | AAGTCTTCCTTCCTG[C/T]CCAATGTAAGAATTA | 67057 |
| rs252562453 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93291474 | ACCACATGGTGGCTC[A/C]CAACCATCTGTAATG | 67057 |
| rs252627632 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93298035 | TATGTCCATATGTGT[A/G]CCTAGGTGCTTGCAA | 67057 |
| rs252682540 | in-del | -/GTTTTTT | | | intron-variant | Yaf2 | Mm_Celera | 15:93330544 | CTTTGTATACAGTGG[-/GTTTTTT]GTTTTTTGTTTTTTG | 67057 |
| rs252697548 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Yaf2 | Mm_Celera | 15:93285493 | GCCCTGGCTGTGCTG[A/G]TCGCCAGCAGCGCTG | 67057 |
| rs252826042 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93300860 | CAGGTGCATATGGAC[A/G]TGTGGATGCATGTGC | 67057 |
| rs252828970 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93334386 | CCAAACACAGATCTC[A/G]GGGCGGGGGGGGGGG | 67057 |
| rs252863917 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93290015 | GGCCTCGGGGTCTTC[C/T]TTGCAGCTCTGTTCC | 67057 |
| rs252908718 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93324683 | TGTTCTGATATCATG[A/G]GTAAGCACACTGGAA | 67057 |
| rs252950686 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93324346 | ACAGAGCGCTCCAGC[A/C]CAGAATGCTTCCAGA | 67057 |
| rs252968009 | snp | G/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93287558 | CGCACACACGGGATG[G/T]AGATATAAAATTAGT | 67057 |
| rs252992446 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93301222 | TCCCCCGTCCCCCCC[C/T]CTTAATTTCCCTGTA | 67057 |
| rs253049493 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93296954 | GAGAAGCGGTAGGAG[A/G]AAGTTCTCCTCCTCT | 67057 |
| rs253051884 | in-del | -/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93335497 | AAAATTCCCCGTATT[-/C]TGTAATCATTTGTAT | 67057 |
| rs253092974 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | Yaf2 | Mm_Celera | 15:93284384 | ATTGAAGGTTGTATC[-/T]GGAACTAGAGTACTG | 67057 |
| rs253097254 | in-del | -/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93313828 | AGCAAATGCTCAAAA[-/T]TCTCAGCACTAACGA | 67057 |
| rs253126768 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93332545 | GCTAACTCAGATTTT[A/G]TATAACCAAATATAC | 67057 |
| rs253137134 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93320605 | AGGCCTGGGATTCTA[C/T]CTCTAGCTGTCTCTT | 67057 |
| rs253152700 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93292046 | AACCAACAGAACTAA[C/T]TGAATCTGTCAGAGG | 67057 |
| rs253159248 | in-del | -/GGA | | | upstream-variant-2KB | Yaf2 | Mm_Celera | 15:93337677 | TTTGGGTGTGCTGAT[-/GGA]GGAGGCGTTGTAGCC | 67057 |
| rs253223186 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93328527 | TATATTCAACGACCT[C/T]CCCAGACCTGGTCCC | 67057 |
| rs253252326 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93333012 | AAAGCCAGCTATAGA[A/G]GAGACGAGGACAATG | 67057 |
| rs253294924 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93302067 | TTTACAAAAGGGCTG[C/T]GGTTTGCTTCCTAGG | 67057 |
| rs253308861 | in-del | -/AA | | | intron-variant | Yaf2 | Mm_Celera | 15:93285631 | CTTGGTCTAAACACA[-/AA]AAAAAAAAAGCAATG | 67057 |
| rs253371900 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93330012 | ATGCCAAGGAGGTCA[A/G]AAGAGGGCTTCATAT | 67057 |
| rs253375288 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93310420 | TCTTCCACATCACTG[C/T]TCATCATGGAAGTCA | 67057 |
| rs253382564 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93307249 | GGGCCCAGTGAACCC[A/G]AAGCCAAATGACTGA | 67057 |
| rs253384781 | snp | A/G | | | upstream-variant-2KB | Yaf2 | Mm_Celera | 15:93338660 | CGTGTGATGGTGTTG[A/G]GTCCCCTGGAACTAG | 67057 |
| rs253417890 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93301823 | CAGCCTAGGCAAGCA[C/T]CTACCAGATGGGAGG | 67057 |
| rs253481311 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93296992 | AGACCCTGAGGGTCA[A/G]GCTCAGATTATCAGA | 67057 |
| rs253557213 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93296535 | TTCATAACAAAACTG[A/G]GTAGAAAAATTAGTT | 67057 |
| rs253557371 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93302179 | AGGAAGCAGGTCAAC[C/T]AATAGCACAAGGGCC | 67057 |
| rs253611766 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93318301 | TACACTTGTGAACTG[C/T]CATGTGGGTGCTGAG | 67057 |
| rs253611796 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93306746 | CAGGCAGAGGCAGGA[A/G]GATTTCTGTGAGTGC | 67057 |
| rs253647125 | snp | A/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93316406 | GCCAGCCAAGCTGGT[A/T]ACCTCTGTAAGCCTC | 67057 |
| rs253657634 | snp | A/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93295174 | GTGAGAGAGAGAGAG[A/T]GAGAGAGTTAAACAA | 67057 |
| rs253712258 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93307331 | TAGAACAATGGTGTA[C/T]TCCGAATGGTGTAGC | 67057 |
| rs253716564 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93286861 | GGACCTCTGGAAGAG[C/T]AGTCAGTGCTCTTAC | 67057 |
| rs253728445 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93288713 | TTTGTCTGACTCAGG[A/C]AAGTTATGTGAAAAA | 67057 |
| rs253746546 | snp | G/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93293920 | TGTCCAATGGCCTTC[G/T]CGGGAAGGTTGCTTC | 67057 |
| rs253771450 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93286279 | TTTCAAGTGCAGAAA[A/G]CTTCTGTAATATTCT | 67057 |
| rs253793889 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93315197 | GGTGGGGTTGCCATC[A/G]CACAGTCACATCTCT | 67057 |
| rs253807127 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93295799 | TATCTAAAGGACTTC[A/G]GCGACTTTGTGGAGA | 67057 |
| rs253955869 | snp | C/T | | | upstream-variant-2KB | Yaf2 | Mm_Celera | 15:93338575 | GGATTAGCACCTACA[C/T]TAATGATCTCTCTCT | 67057 |
| rs253968443 | snp | C/T | | | upstream-variant-2KB | Yaf2 | Mm_Celera | 15:93337332 | GGGGCTCTGCAGTGG[C/T]TTGTTATAAAACGGA | 67057 |
| rs254128427 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93322772 | TAATAACATAATTTT[A/G]TTCACTTTTCTACCT | 67057 |
| rs254137479 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93320493 | TGCCTAACATGCACA[A/G]CATTGTAGGTTCAAC | 67057 |
| rs254216142 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93331298 | TAGGAGTGACAGACT[C/T]ACCTGAATTTGGTTT | 67057 |
| rs254257561 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93318756 | TTTGCTAGATTCACA[C/T]TTAATTTTATCATGC | 67057 |
| rs254311015 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93288270 | GCATTGGCACAAGGA[A/G]GGCTAAGGATGACAG | 67057 |
| rs254320789 | snp | G/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93292689 | GAGTTTGCAGGTTTG[G/T]GAGTGAAGCTGGCCA | 67057 |
| rs254322114 | snp | A/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93326726 | GATGACAGTTGAGAC[A/T]TAACATTCACATCCC | 67057 |
| rs254469181 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93299852 | AGTTACTGAACGAAC[A/G]GCCCACCAGAGCCCT | 67057 |
| rs254507516 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93298001 | TGTTCCTTCTTGGCT[A/G]TGTGGGGCTGGACAT | 67057 |
| rs254616634 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93295741 | CCTTCTGTCACTTCT[A/G]TGATAATCATTTGGA | 67057 |
| rs254656264 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93300608 | TCTTCTATGATTTAG[A/G]CTGCCTTAGAACTCA | 67057 |
| rs254689733 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93302842 | TGCACCAAAGGGGGC[A/G]AAACTACAGAACGGC | 67057 |
| rs254689899 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93312561 | GCATGGTGGCACGTG[C/T]CTTTAATCCCAGCAT | 67057 |
| rs254718820 | snp | A/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93311520 | TAATACAGAATTATT[A/T]AATTTGTATTAATTT | 67057 |
| rs254781388 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93303603 | CTTCATGAAGTAACG[C/T]GTAACTAAACTGGGT | 67057 |
| rs254849882 | in-del | -/C | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93298813 | CAAAACAAAACAAAA[-/C]AAAAAAATGCCAGCA | 67057 |
| rs254865020 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93329520 | GACAGTACATGAAGA[A/C]TCCCAGTAAATTAGG | 67057 |
| rs254866971 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93291194 | AAAACTATCTGTAAT[C/T]CCAGGTCCCAGTGTC | 67057 |
| rs254885838 | in-del | -/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93334115 | TGTGTGCTGCAGCTG[-/C]CCCCCTCCCTGCTCT | 67057 |
| rs254948590 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93328027 | TTAAAGAAGCATCGT[A/G]AAAACATGTCAGGGC | 67057 |
| rs254958125 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93322302 | TCCTAAAAACAGAAG[A/G]CAGAGGAGCTTCCTC | 67057 |
| rs255119684 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93289164 | ACCAGTGTGCCTCAG[C/T]CAAAGCCACCACAGC | 67057 |
| rs255120259 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93296599 | ACGTAGTGGCGCACG[C/T]CTTTAATCCTAGCAC | 67057 |
| rs255130990 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93311576 | TATAATTTGCTTTTA[A/C]TAAATTTAGAATTTT | 67057 |
| rs255136388 | snp | A/T | | | upstream-variant-2KB | Yaf2 | Mm_Celera | 15:93337071 | GCGCCGCCTCCCTCC[A/T]GCTCGCCCGCCCGCT | 67057 |
| rs255276844 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93327092 | TTACTACTTAAGCTA[C/T]GTGTTCTGCCTGTGT | 67057 |
| rs255276882 | snp | A/G | | | upstream-variant-2KB | Yaf2 | Mm_Celera | 15:93338136 | GCAGAACGGGTGGGA[A/G]TATACAGCTCAGAGA | 67057 |
| rs255315764 | in-del | -/TGTGCATGTGTGTGTGCA | | | intron-variant | Yaf2 | Mm_Celera | 15:93300904 | GGACATGTGGATGCT[-/TGTGCATGTGTGTGTGCA]TGTGGATGCATGTGC | 67057 |
| rs255407149 | in-del | -/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93326888 | CACTCCTCCTCCTCA[-/G]CCACGTAGGGAAGCC | 67057 |
| rs255414373 | snp | G/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93310433 | TGTTCATCATGGAAG[G/T]CAGGACAGGAACTCA | 67057 |
| rs255414456 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93322205 | GTCCTTCAGGGATGG[C/T]TGGAACTCTACAGAC | 67057 |
| rs255488323 | in-del | -/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93327357 | CCTTACCTCTACCCT[-/C]GGGGAGCACAAACTG | 67057 |
| rs255493465 | snp | G/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93334581 | TAGACTTCTGGTGAG[G/T]GGCCCAGAGCCTCTT | 67057 |
| rs255508694 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93294987 | GCTCTTCCCACTGGG[A/G]TGTCACTGGGTACAC | 67057 |
| rs255528464 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93321390 | CAAATCAATTCTAGG[C/T]ACCAAGCTCTAAAAT | 67057 |
| rs255543397 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93296455 | AGCCTGTGCTTCACA[A/G]CCCCGTTGGGTATGG | 67057 |
| rs255610776 | snp | C/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93311239 | GTTAGACTGGGAAAG[C/G]ACTTGTGTTACAGGT | 67057 |
| rs255681330 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93289669 | AAGCAAAGAAGCGGA[A/G]CGGGCTGAGGCTCCT | 67057 |
| rs255808331 | in-del | -/A | | | intron-variant | Yaf2 | Mm_Celera | 15:93309341 | GTAACAGCTCCTGAG[-/A]AAAGACACTAGAGCG | 67057 |
| rs255907062 | in-del | -/T | | | upstream-variant-2KB | Yaf2 | Mm_Celera | 15:93337780 | TGGCTCCTGGGATAC[-/T]ATAAGGTTGTTTAGA | 67057 |
| rs255943699 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93299535 | ACACCTTCAACACAC[A/G]AATGCACATGCACAC | 67057 |
| rs256060637 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93306728 | TTTAACCCCAGCGCT[C/T]GGCAGGCAGAGGCAG | 67057 |
| rs256078636 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93333447 | GTGGCATCTATCGTA[C/T]GAGGATAGCCTCATT | 67057 |
| rs256097314 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93329781 | AGGTAGGCAGTCAGT[C/T]ATCAGACTAAATAAG | 67057 |
| rs256112459 | in-del | -/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93315797 | AGACAGAGAGTGGAT[-/G]TGGGGGGGTGGAATG | 67057 |
| rs256180678 | in-del | -/CCGT | | | intron-variant | Yaf2 | Mm_Celera | 15:93287176 | TAAGTATCTGTAGTG[-/CCGT]CCACTTGGTTCCCTC | 67057 |
| rs256265026 | snp | C/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93322011 | AAGGCTGTCCCTTAC[C/G]CTCCCTTCCAGCTCT | 67057 |
| rs256340252 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93288255 | ACACCTGTGAACCCA[A/G]CATTGGCACAAGGAG | 67057 |
| rs256350631 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93323754 | GGACGGGCTGGAGAG[A/C]GTGGCTTAAGATGGC | 67057 |
| rs256357911 | snp | G/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93326501 | ATCGTTCAAAGCAGA[G/T]GACTGTTTATGTCAT | 67057 |
| rs256395600 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93335301 | TATTGAGATTTATGA[C/T]AGGTATGTCAAAAAC | 67057 |
| rs256418427 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93287528 | CACGCATGCGCACGC[A/G]CGCACACACGCACAC | 67057 |
| rs256468029 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93313673 | ATAAAGGTAAAAGCT[A/G]CAGCTGTTAATATTG | 67057 |
| rs256499362 | in-del | -/GT | | | intron-variant | Yaf2 | Mm_Celera | 15:93301213 | ACGGAGCCGTCCCCC[-/GT]CCCCCCCTCTTAATT | 67057 |
| rs256520485 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93292604 | TGCACTATGAAGCCA[C/T]GGGCCTCTATTCTAC | 67057 |
| rs256765256 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93310259 | GAGGGAAATAGTTCC[A/C]AAAAGTTGTCCTCTG | 67057 |
| rs256766491 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93301319 | ATCCCTTACTACTTT[A/G]TTCTATCTCATCTTA | 67057 |
| rs256833847 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93302230 | ATGAAAGTGCCAGGC[A/G]TGGCGGTGCACAGTA | 67057 |
| rs256920000 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93305813 | AGGTAGATCCTTAAG[A/G]ACCACAGTGGGGACT | 67057 |
| rs256975176 | in-del | -/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93286140 | AATTTCAAGTACCTA[-/T]TTTTTTTTAATTGAT | 67057 |
| rs257018833 | in-del | -/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93296179 | AAATAAATGTTCTAA[-/G]GCAATTTGCTGCAAA | 67057 |
| rs257028369 | snp | A/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93314901 | TCTCGTTTCATCTAA[A/T]GATTAGATATGAACA | 67057 |
| rs257060770 | snp | C/T | | | downstream-variant-500B | Yaf2 | Mm_Celera | 15:93283510 | CAGTAACGGAATGTG[C/T]ACGGCTTCCTGACAG | 67057 |
| rs257114571 | in-del | -/TTGCTTTTTTTT | | | intron-variant | Yaf2 | Mm_Celera | 15:93310543 | ACTCAGCTTGCTTGC[-/TTGCTTTTTTTT]TTTTTTTTTTTTTTT | 67057 |
| rs257152328 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93331479 | TTGGCCTTCAGTACC[A/G]CGCTCTATGTACTTC | 67057 |
| rs257305385 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93297874 | GTGTGCACCACCACG[C/T]CCGGCTACATATAAT | 67057 |
| rs257320068 | in-del | -/TTTT | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93306030 | AGCTTTTAACTTTAA[-/TTTT]AATTTTTTTCCCTTG | 67057 |
| rs257350443 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93286403 | AACCCCACGGAGCCC[A/G]CTCTACCTGGTTTTC | 67057 |
| rs257376927 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93319300 | AGACCAGGCTAGCTT[C/T]GGACTCAAGAGATCC | 67057 |
| rs257385317 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93291734 | AGAAAACAATCCTAG[C/T]GCTCCAACTCACAAA | 67057 |
| rs257387345 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93298827 | ACAAAAAAATGCCAG[C/T]AGTGACGTGAGAAAG | 67057 |
| rs257426743 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93298255 | GCGTGTGTTTGTATT[A/C]TATGTATGCCCAGTT | 67057 |
| rs257434425 | snp | C/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93327237 | ACTCGTGAGCCTCTG[C/G]AAAGCTTTAAGGAAG | 67057 |
| rs257530891 | snp | C/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93320151 | AAACAAACAAAAAAC[C/G]GAACAAACAGAAAAA | 67057 |
| rs257647934 | in-del | -/CCGCG | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93336686 | ACACACGCGCGCGCC[-/CCGCG]CCGCGCCGCGCCGCT | 67057 |
| rs257701440 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93325404 | TTCATTATTTTACTG[A/G]AGACATGTAAAAATT | 67057 |
| rs257792497 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93324529 | TTTTTGAATTCCTCC[A/C]TGCTCATGCCTCCCC | 67057 |
| rs257802615 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93298106 | ATAAATTGTTAAGTC[A/C]AGCCATCATAAAGGC | 67057 |
| rs257840300 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93303982 | AAAATTCCCAGGCAG[A/G]CTCAGTGTGTAAGTG | 67057 |
| rs257941345 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93292418 | GGGGAAGGCCTTTCA[C/T]GTGACATCCATTTCT | 67057 |
| rs257950692 | snp | A/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93332899 | CAATCATCAGCAATT[A/T]CTACCTTCACAGGCA | 67057 |
| rs258037333 | snp | C/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93299306 | AGCCAAGTAATTGTG[C/G]CAAGTGCCTGTAATC | 67057 |
| rs258040147 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93333279 | CTTCTCATAAAAGCA[C/T]GATATAGAAATTTAA | 67057 |
| rs258081577 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93324396 | TCAGCACACACTGCT[C/T]AACATCCTACACTAC | 67057 |
| rs258138401 | snp | C/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93333119 | ATGCCTGCAATCCCA[C/G]CACTCAGGAGGCTCC | 67057 |
| rs258144485 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93323498 | TCCTCAACGGCTGCA[A/G]TTACTTCTCCTAAAT | 67057 |
| rs258160788 | snp | C/T | | | downstream-variant-500B | Yaf2 | Mm_Celera | 15:93283359 | ACACATTCAGGCAAG[C/T]AAAATACTCACACAT | 67057 |
| rs258278494 | in-del | -/CAAA | | | intron-variant | Yaf2 | Mm_Celera | 15:93316951 | AGTGAGCACCTGTCT[-/CAAA]CAAACAAACAAAGCT | 67057 |
| rs258280126 | snp | A/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93291076 | TACTTACAAAATTAC[A/T]AAGTGGAAATCCTAG | 67057 |
| rs258284380 | in-del | -/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93308594 | ATTAACATTCAAATA[-/C]AGAATAAATTTTTCT | 67057 |
| rs258314524 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93290487 | ACCTATGCTAGAAAC[A/C]CCATCAGAAAGGCAG | 67057 |
| rs258319089 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93308974 | TAGTGTATGCTAAGA[C/T]TCATGTGTTAGAAGC | 67057 |
| rs258412711 | in-del | -/A | | | intron-variant | Yaf2 | Mm_Celera | 15:93335961 | CCATTACGATCCTAC[-/A]AGCGATACTTTTTCC | 67057 |
| rs258527221 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93301616 | TTTATACCGTAGAGC[A/G]AGCTGCCTACTTGGG | 67057 |
| rs258558051 | in-del | -/AT | | | intron-variant | Yaf2 | Mm_Celera | 15:93298014 | TGTGTGGGGCTGGAC[-/AT]ATACATATGTCCATA | 67057 |
| rs258596428 | snp | A/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93314235 | ATTCAAAAGACTGAC[A/T]TACAATGACTGCATG | 67057 |
| rs258601408 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93333196 | AAGGCTGACTCAAAA[A/G]AATCCCGAGGGGTTT | 67057 |
| rs258614860 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93332882 | GGATACTCGTCTTAA[C/T]TCAATCATCAGCAAT | 67057 |
| rs258626534 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93312257 | ACCAGCCCGGTTCCC[C/T]GTCCACCTGATTCCA | 67057 |
| rs258631138 | snp | A/C | | | upstream-variant-2KB | Yaf2 | Mm_Celera | 15:93337627 | AAGGAGAGATGAAAT[A/C]CATCCCTTCTCGGAG | 67057 |
| rs258631689 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93323864 | GGACCCAATGCCCTC[C/T]TCTGCTGTGTCTGAA | 67057 |
| rs258707457 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93314776 | TTCAAAGAATAAAGG[C/T]ATAAGCACTCTGCCA | 67057 |
| rs258712806 | snp | C/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93314604 | TAGAGGCTGCTCAAT[C/G]TGTAATCCCTCTGAA | 67057 |
| rs258729922 | in-del | -/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93286028 | AAAGCTAGGGCCAGG[-/C]TAACTCTTTACTCCA | 67057 |
| rs258818897 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93305640 | CTGGGGAGGCGGCTC[A/G]GTCAGTAAGATGTCT | 67057 |
| rs258856447 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93331117 | TCACTGGTATCAACA[C/T]CAGTTTTACCAGAAA | 67057 |
| rs258952077 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93294615 | CGCCCAACCCACATC[A/C]GAGGAGCTGCTTCCA | 67057 |
| rs259040180 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93297196 | TCTCCATACAAGCTA[C/T]GATGCTGAACTGAAG | 67057 |
| rs259072170 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93296928 | GCATGCCATGGAGCC[C/T]ATGGAGATCAGAGAA | 67057 |
| rs259076521 | snp | C/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93302625 | TGGTGCACACATTTA[C/G]TCCCAGTGCCGAGGA | 67057 |
| rs259078279 | snp | G/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93325480 | ACAGCCCGCAACTAT[G/T]TTCATCTTGGACATA | 67057 |
| rs259086644 | in-del | -/TGCCAAC | | | intron-variant | Yaf2 | Mm_Celera | 15:93300708 | CTGATTGACTAGCTA[-/TGCCAAC]TGATCCCTGATAAAC | 67057 |
| rs259222965 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93316698 | GCCCTCTTCTGGGGT[A/G]TCTGAAGACAACTAC | 67057 |
| rs259239323 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93319648 | CAGTAAGAGCATTAG[A/G]CACATGCACAGTATT | 67057 |
| rs259250189 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93335902 | CCCAGACGCGAAACC[C/T]TGGCCTGACCCTTTC | 67057 |
| rs259345746 | snp | G/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93323205 | CTCTACATACCTAGA[G/T]CACTGCACAGCTACC | 67057 |
| rs259400678 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93331649 | TAACGCACACTAGAC[A/G]GACACGTTTACCTCC | 67057 |
| rs259402718 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93285953 | TGACACCATGAGTGG[C/T]GTTGGAGGCATGCAC | 67057 |
| rs259433598 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93322640 | TACACTCTGTAACTA[C/T]AAATAAAACTTACAT | 67057 |
| rs259505519 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93323837 | ACATGGTGGCTCACA[A/G]CATCTGGAGTGGGAC | 67057 |
| rs259519028 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93301085 | AGGCCGCAGAGAGTC[A/G]CCTAACAGTCCTCCA | 67057 |
| rs259523997 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93287532 | CATGCGCACGCGCGC[A/G]CACACGCACACGCAC | 67057 |
| rs259533742 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93300199 | AGCCCTGCTTGGATG[C/T]TCTGTGCTTTCTGCA | 67057 |
| rs259609835 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93295437 | TAGGCACCCACCTAC[C/T]CAAGACCTCAGTCTC | 67057 |
| rs259643539 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93300856 | TGTCCAGGTGCATAT[A/G]GACATGTGGATGCAT | 67057 |
| rs259804802 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93307959 | TTTATTTGAGATATA[A/G]AATTTTAATACAATT | 67057 |
| rs259862688 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93321634 | GAATTCTACTCATTA[A/C]GTTTAAACTACTTCC | 67057 |
| rs259939483 | snp | A/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93329082 | AGAAAGTCCAGGCGT[A/T]AGAAGGTGCACGAGT | 67057 |
| rs259952664 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93328389 | GGTGAGAAAGATAGT[A/G]CGAAGGGTGATGAAG | 67057 |
| rs259958205 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | Yaf2 | Mm_Celera | 15:93284420 | TCCATATGAATTGTT[A/T]TATTTAGTAAAAGGC | 67057 |
| rs259972481 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93287432 | AGCTTCACAGAGCTC[A/G]ATTCAGAGGAACAAA | 67057 |
| rs260131400 | snp | A/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93295914 | AAGCCTGCAGACCAG[A/T]GCAGCCTCACTTAGC | 67057 |
| rs260133270 | snp | A/C | | | upstream-variant-2KB | Yaf2 | Mm_Celera | 15:93337538 | ACCAGAGTTAGCTTG[A/C]CATCCCTCTGATCGA | 67057 |
| rs260152762 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93289359 | CTCTACTGAAGGTCC[C/T]GAGTTCAATTCCCAG | 67057 |
| rs260188002 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93299445 | GAAAGTAGAGAGCAA[C/T]TGAGGAAGGCACTCA | 67057 |
| rs260197801 | snp | G/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93292131 | CAACAGGATGGGGTG[G/T]AAGTGAAACAATGGA | 67057 |
| rs260217137 | snp | A/G | | | upstream-variant-2KB | Yaf2 | Mm_Celera | 15:93338646 | TGTATGACTGCGTGC[A/G]TGTGATGGTGTTGAG | 67057 |
| rs260253908 | snp | A/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93294296 | AGTACAGGATGTCAT[A/T]ATGAAATAAACTTCC | 67057 |
| rs260334992 | in-del | -/A | | | intron-variant | Yaf2 | Mm_Celera | 15:93312871 | AAGCCATGGCTGATC[-/A]AAATGCAGAGGACAG | 67057 |
| rs260403711 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93290621 | CTTACTGACATCTAA[C/T]CATGTGTATGTGGTG | 67057 |
| rs260432158 | snp | A/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93335396 | TATAAACTGAGTTTT[A/T]AAAAAAAAAACAGGA | 67057 |
| rs260445376 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93294084 | ATTTTAAGAAGAGCC[A/G]TGTGCTCTTTGGTTT | 67057 |
| rs260445485 | in-del | -/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93303434 | AGGTCTAAGGATATA[-/C]TGCTCAGCGGGAAAT | 67057 |
| rs260451070 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93310686 | TCCCGAGTGCTGGGA[C/T]TAAAGGTGTGCGCCA | 67057 |
| rs260481380 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93315820 | GTGGAATGTTGAGTG[C/T]AAAAAATAAATTAAA | 67057 |
| rs260507852 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93325048 | TCTCCAAAGGAAGTC[A/G]GGACAGGAACTCAAG | 67057 |
| rs260582652 | snp | A/G | | | downstream-variant-500B | Yaf2 | Mm_Celera | 15:93283427 | ATATCACAAATTTCC[A/G]AGACAGCCACAGATG | 67057 |
| rs260583411 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93326883 | ATGGGCACTCCTCCT[C/T]CTCAGCCACGTAGGG | 67057 |
| rs260634072 | snp | C/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93336331 | GATCCACGGGCGCGC[C/G]GGACTCACCGGGTGG | 67057 |
| rs260689942 | snp | C/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93309277 | ACTGGCCAGCTAGCT[C/G]AATCAGCAAATCCCT | 67057 |
| rs260718637 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93320899 | CACTTCAGAACTAAC[A/G]CATAAATAAGCAACT | 67057 |
| rs260751190 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93334045 | GGTTGTTCTGACCCA[A/C]GGGATCCAAATGCTG | 67057 |
| rs260798722 | in-del | -/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93309013 | CAATGTGGTCACCTT[-/G]GGAGGGGTTAGAACT | 67057 |
| rs260850886 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93305795 | CGCTCAATCATGTGG[C/T]TCAGGTAGATCCTTA | 67057 |
| rs260891188 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93288621 | CTTGTCAACTCCTGC[C/T]GCCACAGTTCTCATT | 67057 |
| rs260910765 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93299357 | AGACTGGGGATGCCC[A/G]GGACAAGCTGGCTGG | 67057 |
| rs260924848 | in-del | -/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93310949 | GACTTTATTGACCCC[-/T]TTTTGTTATACAACG | 67057 |
| rs260940069 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93306575 | TGATCATGGTGATGT[A/G]TGCCTTTAATATCAG | 67057 |
| rs260961034 | in-del | -/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93305919 | TATACACGCGCAACA[-/G]GGCTCGCTAGATCTT | 67057 |
| rs260962006 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93290088 | GGAGGGCCCAGCAAA[C/T]CTAGCAATTTCAAGC | 67057 |
| rs261104566 | in-del | -/AATG | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93296723 | GTCCCGAAAAACCAA[-/AATG]AATGAATGAATGAAT | 67057 |
| rs261139608 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93326284 | TTCAAGAAACTGAAC[A/G]ATAAACTCCTACTGC | 67057 |
| rs261166391 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93295858 | CTGTCAACAGCACTC[A/G]CTGTGTGTGAGCCGT | 67057 |
| rs261177704 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93334983 | CTAAAAGTATGAGAG[A/G]ATACAAGTAAAAACA | 67057 |
| rs261195546 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93301181 | GTCCTCAGATTTTTG[C/T]GGCAAACACTGTACT | 67057 |
| rs261279509 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93326173 | AAACCTCATTCTAAG[C/T]ACGGCCTCTTAGAGC | 67057 |
| rs261406078 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93297125 | AATTTTATTACGCAA[C/T]AGTCTATTTGAAAAC | 67057 |
| rs261407169 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93333509 | GCCAAAGAAAGTCAT[C/T]GCCTGTTCCGATACA | 67057 |
| rs261424673 | in-del | -/CTAACTCAATCTG | | | intron-variant | Yaf2 | Mm_Celera | 15:93332518 | CATTACAGTGAGTAC[-/CTAACTCAATCTG]CTAACTCAGATTTTA | 67057 |
| rs261447262 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93321286 | GCAGATATCTGAAAC[A/G]GAGTCACATATAGAC | 67057 |
| rs261460900 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93328869 | TCTCACCATGGACAA[C/T]AGCACAATGCTCCGC | 67057 |
| rs261640634 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93328326 | TAGGACATGGAGAAA[C/T]GAGGCGAGGCTAGTT | 67057 |
| rs261645252 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93314574 | CCAAACACGACACTG[A/G]CGTGCTTGAGTAGGT | 67057 |
| rs261665944 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93324282 | TAGCACAGAGCGCTC[C/T]AGCACAGAGCGCTCC | 67057 |
| rs261670561 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93300790 | ATTCTACTTAGAGTA[A/C]CTTCAAATTCTAGCT | 67057 |
| rs261754324 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93295323 | CTACTTAACATACTG[C/T]CTTAGGAACCGGTGC | 67057 |
| rs261774644 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93296814 | GGTCACAGCAGAGAG[A/G]TGAAGAACCGCTGCT | 67057 |
| rs261788890 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93331598 | TCACTAGGTGGGGAA[A/G]GGTACGATGAAACCT | 67057 |
| rs261796206 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93291442 | TCTTCCAGAGGTCCT[A/G]GGTTCAATGCCCAGC | 67057 |
| rs261825559 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93309704 | CTAAAAACCATAATT[C/T]TGTTTTTGAGACATC | 67057 |
| rs261852056 | snp | G/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93289725 | CTCCCCTGGGAGCTG[G/T]GATGCCTCTGCTGAG | 67057 |
| rs261889069 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93301870 | AAGGACGGGGCAGCG[C/T]CTGCACATCACATGC | 67057 |
| rs261898081 | snp | A/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93320434 | AGATGCTACCTGGGA[A/T]GAGAGTGGGACTGAG | 67057 |
| rs261906012 | in-del | -/A | | | intron-variant | Yaf2 | Mm_Celera | 15:93335874 | CAGAAATAGAACAAC[-/A]AACAAAAAAAAACCC | 67057 |
| rs261949939 | snp | A/G | | | upstream-variant-2KB | Yaf2 | Mm_Celera | 15:93338395 | CTCCGAGTAGAAGAT[A/G]AAGATGTCAGGGCTG | 67057 |
| rs262019192 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93297847 | TCTGCTTCCCGAGTA[A/C]TGGGATTAAAGGTGT | 67057 |
| rs262081294 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93330577 | TTTGTTTTTTGCAAG[C/T]TTCCCAAAATCTACT | 67057 |
| rs262124140 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93332156 | AGAAACTGAAATAAC[C/T]TGTTACCATTAATCA | 67057 |
| rs262162639 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93322267 | CTTAGAGCTGAACAG[C/T]GGAGTCCTATGAGTC | 67057 |
| rs262198500 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93301268 | TCATTTTCCTGAACT[A/G]CGCGTTGTTTTCTGG | 67057 |
| rs262214255 | in-del | -/GAAA | | | intron-variant | Yaf2 | Mm_Celera | 15:93334250 | TGTCACTCCTAAGAG[-/GAAA]CACTGTGCATGTAAC | 67057 |
| rs262217879 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93308440 | AGATGGCCAGGGAGT[A/G]AGAAAGGGTTTTCTG | 67057 |
| rs262235355 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93297572 | TTGAAAGAAAAAGAC[A/G]GACTTTTCAAGAGGG | 67057 |
| rs262256427 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93298604 | TGTCTTACACAGAGC[A/C]ACCATGTTCTGCACA | 67057 |
| rs262525871 | in-del | -/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93322863 | AGAGGCCGAGAGCCC[-/T]TGATGTGGTAAATGA | 67057 |
| rs262526889 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93299745 | CAGCGGCTGGGTGCT[A/G]GCTTCATTAGGTAAC | 67057 |
| rs262550169 | in-del | -/C | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93298505 | TGAGCCAGCCAGCCA[-/C]CAGCATTAGAGAACT | 67057 |
| rs262551282 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93329362 | CCTACAAGGACCATT[A/G]TTATATAGGATTTTT | 67057 |
| rs262603811 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93333659 | ATGTAAGTATACAGT[A/G]CATGTGTGTACATAC | 67057 |
| rs262608836 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93331759 | CTCCCAAGGTTCCTC[C/T]TCTGACACTCTGAAA | 67057 |
| rs262621593 | in-del | -/AAAAAAA | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93287599 | GGAAATCCTATCCTG[-/AAAAAAA]AAAAAAAAAAAAAAA | 67057 |
| rs262668196 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93324773 | AGCTAACCCTTTTTA[A/G]TCATTACTTTCATTT | 67057 |
| rs262710981 | snp | C/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93297393 | GAGAAAACTGTTCTT[C/G]AAGAGAGGATGTTTC | 67057 |
| rs262728306 | in-del | -/GGA | | | intron-variant | Yaf2 | Mm_Celera | 15:93308644 | ATTTTTATAAAAATT[-/GGA]GATTTGTAGGACACT | 67057 |
| rs262729608 | snp | A/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93302788 | TGCCCAATGAAAGAA[A/T]GGGAAGAAGACTATT | 67057 |
| rs262783059 | in-del | -/TTTAAC | | | intron-variant | Yaf2 | Mm_Celera | 15:93306019 | TATCCCTCCTTAGCT[-/TTTAAC]TTTAATTTTAATTTT | 67057 |
| rs262827054 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93310901 | AAAGATGTTTATCTC[A/G]TTTCTCTTCCTCTCC | 67057 |
| rs262848983 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93322118 | ATCTCCACAGCTGAA[A/G]TCTTAGGTGGTTTCT | 67057 |
| rs262859492 | in-del | -/CA | | | intron-variant | Yaf2 | Mm_Celera | 15:93291243 | TACTGTCTCACACAC[-/CA]CACACACACACACAG | 67057 |
| rs262871089 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93313353 | GTAAGCTCATCAATG[A/G]TCATGCCGTCAGAGC | 67057 |
| rs262949552 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93298260 | TGTTTGTATTCTATG[C/T]ATGCCCAGTTCAAGC | 67057 |
| rs262967280 | snp | G/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93304394 | ATAGAGCATTTATGG[G/T]GCAAAGTCAACAGAA | 67057 |
| rs263000770 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93315253 | GAATTACAGGAATGG[A/G]AATGGAGAGGACACT | 67057 |
| rs263129490 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93310369 | GAAACACCATGGCCA[A/G]AGGAATCTGGGGAGA | 67057 |
| rs263163840 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93334530 | GCTCAGAGGGACACC[A/G]TTCTGAGCACCTACT | 67057 |
| rs263178985 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93287004 | TATCCAAGAAAATAA[A/G]GCACACATAATACAA | 67057 |
| rs263233725 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93303623 | CTAAACTGGGTACAT[A/G]TCTGATTATGTCCTC | 67057 |
| rs263365198 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93312652 | TTGAGTTCCAAGCCA[A/G]GGCTACATCTTGAGA | 67057 |
| rs263384521 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93314948 | TCTAGAGACACTCAA[A/G]TCTGCCAAAGAGCAT | 67057 |
| rs263412095 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93333769 | TTACATGTGTGCACA[C/T]ACATGTATGTAAGTA | 67057 |
| rs263417502 | in-del | -/A | | | intron-variant | Yaf2 | Mm_Celera | 15:93294877 | CGTTACACCCTAAAC[-/A]GACCTACAGAGGTTC | 67057 |
| rs263550205 | snp | G/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93300750 | CATCATTTATACCCA[G/T]GTTACTTTCTTTCTT | 67057 |
| rs263570759 | snp | C/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93307585 | CTCAAAATATCCTCA[C/G]AAAGAGATCAGCTAC | 67057 |
| rs263668125 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93285846 | ATTGCTCAATGGTTA[A/G]GAGCGCTAGCTGTTT | 67057 |
| rs263701113 | snp | C/G | | | upstream-variant-2KB | Yaf2 | Mm_Celera | 15:93337173 | CGTGCGCCCGGCGCG[C/G]CGGGGACTGTCATCC | 67057 |
| rs263821364 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93300034 | TTGCTAACACACTGT[C/T]GAATTTTTGGTTTTT | 67057 |
| rs263826809 | snp | A/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93295162 | GTGTGTGTGTGTGTG[A/T]GAGAGAGAGAGAGAG | 67057 |
| rs263850282 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93324028 | TCTCAGCTCCTCAGC[A/G]AGGTGCAGACAGGCA | 67057 |
| rs263870273 | in-del | -/TGGT | | | intron-variant | Yaf2 | Mm_Celera | 15:93295089 | GTTTCATTTTGGTGG[-/TGGT]GGGGGGGTTCTGTTT | 67057 |
| rs263916707 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93314318 | TTGTCTTCACATTAA[A/G]ATTTATATACAATCT | 67057 |
| rs263920544 | snp | G/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93325864 | TACAGACATGTTCCT[G/T]CATGTGCTGCTCTTC | 67057 |
| rs263949843 | snp | G/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93291116 | GACAGTTCAGCCAAT[G/T]AAGAGCACTTACGGC | 67057 |
| rs263983801 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93317202 | ACCTATGCATATATC[C/T]ATTAATAGCTTGCTA | 67057 |
| rs264030410 | snp | G/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93319964 | AAACATTTCATCACA[G/T]ACTCAATCTGAACTG | 67057 |
| rs264089369 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93287390 | CTGGCTTGAGCAAGC[A/G]TCCCATCAGTCAGAC | 67057 |
| rs264094278 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93308233 | AGCTTGGGGGGAGGG[A/G]GGAGATAACCAAATT | 67057 |
| rs264097673 | snp | A/G | | | intron-variant, nc-transcript-variant, missense | Yaf2 | Mm_Celera | 15:93317600 | GCAATAGCTTCAGAG[A/G]ATGTGGATCTGTGGA | 67057 |
| rs264197300 | snp | G/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93292700 | TTTGGGAGTGAAGCT[G/T]GCCACGGGGCAAGCA | 67057 |
| rs264276055 | snp | G/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93319153 | AGTATCCACCTTCAT[G/T]GATTTGTTATTGAAA | 67057 |
| rs264386456 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93325496 | TTCATCTTGGACATA[A/G]CTGGAGCCTCCCCTG | 67057 |
| rs264406425 | snp | C/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93289657 | GAAGAAGGGAAGAAG[C/G]AAAGAAGCGGAGCGG | 67057 |
| rs264514378 | in-del | -/AG | | | intron-variant | Yaf2 | Mm_Celera | 15:93297424 | AGCTAGTCCCTGGGC[-/AG]AGTTTCAGTAAGCAA | 67057 |
| rs264518798 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93321366 | GCAACAAGTGCTCTT[C/T]ACCGCCTTCAAATCA | 67057 |
| rs264524998 | in-del | -/GTCTT | | | intron-variant | Yaf2 | Mm_Celera | 15:93330708 | CTAAAGAAGAAAAGG[-/GTCTT]GTCTTGTCTTTTCTT | 67057 |
| rs264531330 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93300124 | TTTCCCTTACTAATA[A/G]ACAAATTGTTTTTAG | 67057 |
| rs264599873 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93333825 | TATGTAAGTATACAG[C/T]GCGTGTGTGTACATA | 67057 |
| rs264619605 | in-del | -/AACAAAAAC | | | intron-variant | Yaf2 | Mm_Celera | 15:93317249 | TTTCATGACCAAAAA[-/AACAAAAAC]AAAAACAAAAACAAA | 67057 |
| rs264629964 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93289072 | CTGTCCATGGTGGTG[C/T]GTCTCCTTTCCTGCC | 67057 |
| rs264651255 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93325471 | GGCCTCTCAACAGCC[C/T]GCAACTATTTTCATC | 67057 |
| rs264669021 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93327319 | GGTGGGCAAGTATCC[C/T]CAGAGTTTCCTATGT | 67057 |
| rs264719888 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93294490 | CTGAGTGAGCTACAC[A/G]GTGAAGTCGACCCCA | 67057 |
| rs264761831 | in-del | -/GAGAGAGA | | | intron-variant | Yaf2 | Mm_Celera | 15:93295142 | AGAGTGAGAATGAGT[-/GAGAGAGA]GAGTGTGTGTGTGTG | 67057 |
| rs264782054 | in-del | -/GTT | | | intron-variant | Yaf2 | Mm_Celera | 15:93335678 | TAACTCTTTTAAATG[-/GTT]TTTTTTTTTTTTTTT | 67057 |
| rs264848406 | snp | A/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93296212 | AAAAAAAAAAAAAAA[A/T]AATTGTGACCCTGGT | 67057 |
| rs264886914 | in-del | -/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93327600 | CTGTGGAGAATTTTC[-/G]TAACTGCTAACTGAC | 67057 |
| rs264889816 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93323018 | GTTCTTCAGTGCTCA[C/T]TGTCTAGCACTGGAG | 67057 |
| rs264900487 | in-del | -/GGA | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93334405 | CGGGGGGGGGGGGGG[-/GGA]GGGGGGGAGCAAAGG | 67057 |
| rs264934069 | snp | G/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93329449 | GAAATGGCACGGGAT[G/T]GTGAACTGTAACTAG | 67057 |
| rs264992160 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93300876 | TGTGGATGCATGTGC[A/C]TGTGTGTGCATATGG | 67057 |
| rs265063348 | in-del | -/A | | | intron-variant | Yaf2 | Mm_Celera | 15:93305703 | CTAGAAGCCGTGTAT[-/A]AAAAACCCGGAGTGC | 67057 |
| rs265069354 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93307780 | CTGTACTATATGAAA[A/G]TGGCCTAAACCAAGT | 67057 |
| rs265094939 | snp | C/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93330138 | CTCTGAGCCACCTCT[C/G]CAGCCTCTGTTTATG | 67057 |
| rs265144893 | snp | A/C | | | upstream-variant-2KB | Yaf2 | Mm_Celera | 15:93338860 | GCCCGGCTTAGAGTT[A/C]CAGTTTTAACCCACC | 67057 |
| rs265231943 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93332580 | GAAACTTTGCTGAAT[A/G]CCACAGTTCAAATGA | 67057 |
| rs265257274 | in-del | -/TGGGAA | | | intron-variant | Yaf2 | Mm_Celera | 15:93330076 | CAGCCATGTAGGTGC[-/TGGGAA]TTGAACCATGATCCT | 67057 |
| rs265279760 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93297806 | TTGTAGACCAGGCTG[A/G]CCTCGAACTCAGAAA | 67057 |
| rs265314280 | snp | C/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93305749 | GCACCCGGAAGACAG[C/G]CAGGAGGACCTCTGC | 67057 |
| rs265366821 | in-del | -/GA | | | upstream-variant-2KB | Yaf2 | Mm_Celera | 15:93338601 | CTCTCTCTCTCTCTC[-/GA]CTTATATAGGCATCG | 67057 |
| rs265378240 | in-del | -/A | | | intron-variant | Yaf2 | Mm_Celera | 15:93333152 | CTAGAGGAATGCTGT[-/A]TGCTCAAGGTTAGCC | 67057 |
| rs265456565 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93290985 | TAAATTATAGCTTTG[C/T]CACGTTCATATACTG | 67057 |
| rs265487753 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93289780 | ATTGCTGAGTTCCTG[C/T]GTCTCAGGATACCCT | 67057 |
| rs265521269 | snp | A/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93304154 | TGAGAAAGTAAATTC[A/T]AGAGCAATGAGTGAA | 67057 |
| rs265531778 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93313704 | CCTAGCAAGTCTGTG[A/G]TAGGTAAGCACTCAA | 67057 |
| rs265601400 | in-del | -/TC | | | intron-variant | Yaf2 | Mm_Celera | 15:93287888 | TCTGTCTTTTATCTT[-/TC]TTTTTTCCTGAAGTA | 67057 |
| rs265730136 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93335172 | AGCAAGTAGTTTCTC[C/T]TTTTAGAATCTTTCC | 67057 |
| rs265870080 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93324486 | GACGATCGACATCAG[C/T]ATACCAGAAAATTCA | 67057 |
| rs265887932 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93298195 | AAATTTATATAGACT[A/G]TCTAACATTTTTACA | 67057 |
| rs265929633 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93291558 | TGTATAGCACTGATA[A/G]TCACTATAAGTAGTG | 67057 |
| rs265941059 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93293623 | TAAAATTCCCTACTG[C/T]TCTTTAGAGAATGAA | 67057 |
| rs265983914 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93286351 | GTACAATCAAAGTTT[A/C]AAAAGGAATATTAAA | 67057 |
| rs265987189 | in-del | -/A | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93289445 | TCTGAAGACAGCTAC[-/A]GTGTACTCATTATAA | 67057 |
| rs266006453 | snp | A/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93314838 | TTACAGAGGTGCATT[A/G]CGGCACATTGGTAAT | 67057 |
| rs266059556 | snp | G/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93307340 | GGTGTACTCCGAATG[G/T]TGTAGCTTGCATATG | 67057 |
| rs266147310 | snp | A/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93320525 | CCCAGCAGTCAACAT[A/C]AGAACCTGGGTAGGA | 67057 |
| rs266211049 | snp | C/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93288307 | CTCATTGGACACCAG[C/T]GCAGCAAGTTCCAGG | 67057 |
| rs386846942 | in-del | -/CA | | | intron-variant | Yaf2 | Mm_Celera | 15:93293381 | TGCATAAAGCTGTCA[-/CA]GAGTAAAGTTACTTT | 67057 |
| rs386913908 | in-del | -/A | | | intron-variant | Yaf2 | Mm_Celera | 15:93289590 | CCCTGGACCGTCCAA[-/A]TAAATCTCTTTTATG | 67057 |
| rs386934642 | in-del | -/ATGA | | | intron-variant | Yaf2 | Mm_Celera | 15:93296752 | TGAATGAATGAATGA[-/ATGA]TTTTACACTCGAAGG | 67057 |
| rs386989878 | in-del | -/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93301534 | ATCCTGTGTCTTGGG[-/G]ATGACACTTGTGGAC | 67057 |
| rs387071058 | in-del | -/AATTTT | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93306034 | TTTAACTTTAATTTT[-/AATTTT]TTTCCCTTGAATATT | 67057 |
| rs387084576 | in-del | -/CAA | | | intron-variant | Yaf2 | Mm_Celera | 15:93305203 | AAACAAAAAAACAAA[-/CAA]ACAAAAAAAAACCAT | 67057 |
| rs387127896 | in-del | -/TCTCTC | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93313937 | CTCTCTCTCTCTCTC[-/TCTCTC]CTCCCTCCCTCTCTC | 67057 |
| rs387176676 | in-del | -/TG | | | intron-variant | Yaf2 | Mm_Celera | 15:93289826 | TCTCCCTCGGCTGTG[-/TG]GTTCCTGGGCTTCCA | 67057 |
| rs387240090 | in-del | -/CTCACCCTCTCC | | | downstream-variant-500B | Yaf2 | Mm_Celera | 15:93283665 | GTCCTCACCCTCTCC[-/CTCACCCTCTCC]ATTGTGAGATACACT | 67057 |
| rs387283030 | in-del | -/AG | | | intron-variant | Yaf2 | Mm_Celera | 15:93297426 | CTAGTCCCTGGGCAG[-/AG]TTTCAGTAAGCAATG | 67057 |
| rs387295256 | in-del | -/A | | | intron-variant | Yaf2 | Mm_Celera | 15:93294245 | TCAACTCCACTGAGA[-/A]CAGGGTCTTTAATGG | 67057 |
| rs387350404 | in-del | -/C | | | intron-variant | Yaf2 | Mm_Celera | 15:93298506 | GAGCCAGCCAGCCAC[-/C]AGCATTAGAGAACTT | 67057 |
| rs387400444 | in-del | -/T | | | intron-variant | Yaf2 | Mm_Celera | 15:93304572 | GGAATACACTAAGTT[-/T]AAGACAGCTACACGC | 67057 |
| rs387438860 | in-del | -/GT | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93305245 | TTAACATATATATAT[-/GT]TTTATATATTTATGT | 67057 |
| rs387440968 | in-del | -/AAAAC | | | intron-variant | Yaf2 | Mm_Celera | 15:93305499 | AAAAAACAAAAAAAA[-/AAAAC]TGGAATATAGCCCTA | 67057 |
| rs387490956 | in-del | -/A | | | intron-variant | Yaf2 | Mm_Celera | 15:93292480 | CAGATTAAAAAAAAA[-/A]CAAAACCAGATTTAA | 67057 |
| rs387499081 | in-del | -/GAG | | | intron-variant | Yaf2 | Mm_Celera | 15:93308645 | TTTTTATAAAAATTG[-/GAG]ATTTGTAGGACACTT | 67057 |
| rs387563253 | in-del | -/GT | | | intron-variant | Yaf2 | Mm_Celera | 15:93289825 | TCTCCCTCGGCTGTG[-/GT]GTTCCTGGGCTTCCA | 67057 |
| rs387678288 | in-del | -/A | | | intron-variant | Yaf2 | Mm_Celera | 15:93285640 | AACACAAAAAAAAAA[-/A]GCAATGAGTTCTTAA | 67057 |
| rs387715177 | in-del | -/G | | | intron-variant | Yaf2 | Mm_Celera | 15:93296180 | AATAAATGTTCTAAG[-/G]CAATTTGCTGCAAAA | 67057 |
| rs387757395 | in-del | -/AA | | | intron-variant | Yaf2 | Mm_Celera | 15:93304764 | AAAGGAAAAAAAAAA[-/AA]ACACAAGCAATTAAA | 67057 |
| rs387858343 | in-del | -/A | | | intron-variant | Yaf2 | Mm_Celera | 15:93308781 | TTTGTTTAAAAAAAA[-/A]TTAGTACTCATGAAG | 67057 |
| rs387861268 | in-del | -/AAGT | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93305543 | GCTTGTGGTAGGATT[-/AAGT]GTTTCCATGAATATT | 67057 |
| rs578435471 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93305614 | TTCTCTAATATACAA[C/T]AACAACAGAACTGGG | 67057 |
| rs578449759 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93332515 | CCTCATTACAGTGAG[C/T]ACCTAACTCAATCTG | 67057 |
| rs578455424 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93296746 | AATGAATGAATGAAT[A/G]AATGAATGATTTTAC | 67057 |
| rs578471244 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93319970 | TTCATCACAGACTCA[A/G]TCTGAACTGTAAAAA | 67057 |
| rs578555828 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93329063 | TCTCCTGCAGATGCA[A/G]GAGAGAAAGTCCAGG | 67057 |
| rs578677047 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93311160 | GTATGCCACCACGCC[C/T]GGCTGACATGTTTTT | 67057 |
| rs578704169 | snp | A/G | | | upstream-variant-2KB | Yaf2 | GRCm38.p3 | 15:93338782 | GACCAGGCTGGCCTC[A/G]AACTCAGAAATCTGC | 67057 |
| rs578771607 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93315745 | GGGCATCCACATGGA[A/G]ATGGGGTGGGGTGGG | 67057 |
| rs578773770 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93296709 | CACAGAGAAACCCTG[C/T]CCCGAAAAACCAAAA | 67057 |
| rs578781479 | snp | A/C | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93333690 | GCTATGTAGGTATAC[A/C]GTACATGTGTGCACA | 67057 |
| rs578819816 | snp | A/C | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93306190 | TCTGTGTAGCCCTGG[A/C]TGTCCTGAAATTCAC | 67057 |
| rs579010091 | snp | A/C | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93295884 | GCCGTCTTTGGAAGG[A/C]GGTACCCAGAGGTCA | 67057 |
| rs579011513 | snp | C/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93314168 | AACTGATAATATTTG[C/G]TGGGGAAGAAGAGAA | 67057 |
| rs579034783 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93298012 | GGCTGTGTGGGGCTG[A/G]ACATACATATGTCCA | 67057 |
| rs579132349 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93333890 | ACACGTATGTAAGTA[C/T]ACAGTACATGTGTGC | 67057 |
| rs579245577 | snp | A/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93316748 | GATAAATAAATCTTT[A/T]TAAAAAAAAAAAAAT | 67057 |
| rs579281609 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93296726 | CCGAAAAACCAAAAT[A/G]AATGAATGAATGAAT | 67057 |
| rs579336230 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93328385 | TGCAGGTGAGAAAGA[C/T]AGTACGAAGGGTGAT | 67057 |
| rs579348455 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93295942 | AGCATCTTCTTCCCT[A/G]CTCCACCCTTCCTCC | 67057 |
| rs579389922 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93297791 | GTCCTGGAACTCACT[C/T]TGTAGACCAGGCTGA | 67057 |
| rs579402325 | snp | A/C | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93315296 | GTCCAGCAACAGGCC[A/C]AAAGTGGGATCCAGC | 67057 |
| rs579505939 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93324192 | ACGCTCGGACCAACC[A/G]TTCCCGTAGGAAGAA | 67057 |
| rs579507943 | snp | C/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93297516 | GCCCAAAGATTCACA[C/G]AATTTACAAAGCACT | 67057 |
| rs579628377 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93287552 | CGCACACGCACACAC[A/G]GGATGGAGATATAAA | 67057 |
| rs579678486 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93315418 | CAAGCAGCTGAAAGA[A/G]TCAGATGCAGATATT | 67057 |
| rs579708137 | snp | G/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93296628 | ACTGGGGAGGCAGAG[G/T]CAGGCGGATTTCTGA | 67057 |
| rs579718625 | snp | A/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93308603 | TCAAATAAGAATAAA[A/T]TTTTCTGGAATTTTA | 67057 |
| rs579814567 | snp | G/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93300056 | TTGGTTTTTTTTTTT[G/T]TTTTTTTGGAATGAA | 67057 |
| rs579821959 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93330243 | CTGCAGCCTCTGTTT[A/G]TGTGTGCGCATCTGT | 67057 |
| rs579910252 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93289819 | GACACCTTCTCCCTC[A/G]GCTGTGTGGTTCCTG | 67057 |
| rs579956887 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93310644 | GACCAGGCTGGCCTC[A/G]AACTCAGAAGTCCGC | 67057 |
| rs579992329 | snp | C/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93297430 | GTCCCTGGGCAGTTT[C/G]AGTAAGCAATGCTGA | 67057 |
| rs579994613 | snp | G/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93320408 | ATGCCGGGCTTTCTG[G/T]CTATACAGTCAGATG | 67057 |
| rs580149756 | snp | A/C | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93299556 | ACATGCACACATACA[A/C]GTACCCCTCATATCA | 67057 |
| rs580198298 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93330188 | TGGACACCTCTGCAG[C/T]CTCTGTTTATGTGTG | 67057 |
| rs580248210 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93315573 | ATCTCTCAAACACTG[A/G]ACCACCAAACAGACA | 67057 |
| rs580250450 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93296648 | CGGATTTCTGAGTTT[A/G]AGGCCAGCCTGGTCT | 67057 |
| rs580262898 | snp | G/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93322376 | ATTTCCTTCCATAAA[G/T]TTTATACACACACAC | 67057 |
| rs580293285 | snp | A/C | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93297438 | GCAGTTTCAGTAAGC[A/C]ATGCTGAGAAGCGGG | 67057 |
| rs580523843 | snp | A/C | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93286775 | GCTGTCTTCAGACAC[A/C]CCAGAAGAGGTGTCA | 67057 |
| rs580607394 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93311147 | TGGGACTAAAGGCGT[A/G]TGCCACCACGCCCGG | 67057 |
| rs580642971 | snp | G/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93299898 | CACACTTCTGATTTC[G/T]GAGACTTTAAGTATA | 67057 |
| rs580648753 | snp | C/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93330230 | ATACTGGACACCTCT[C/G]CAGCCTCTGTTTATG | 67057 |
| rs580662103 | snp | A/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93290369 | TATGGTACATAGTCT[A/T]TGTTAATAAATAAAC | 67057 |
| rs580667082 | snp | C/T | | | upstream-variant-2KB | Yaf2 | GRCm38.p3 | 15:93338770 | ACTCACTTTGTAGAC[C/T]AGGCTGGCCTCGAAC | 67057 |
| rs580839960 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93315743 | GGGGGCATCCACATG[A/G]AGATGGGGTGGGGTG | 67057 |
| rs580960640 | snp | C/T | | | upstream-variant-2KB | Yaf2 | GRCm38.p3 | 15:93338795 | TCGAACTCAGAAATC[C/T]GCCTGCCTCTGCCTC | 67057 |
| rs580974501 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93333139 | CAGGAGGCTCCGGCT[A/G]GAGGAATGCTGTATG | 67057 |
| rs581017956 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93313841 | AAATCTCAGCACTAA[C/T]GAGGAGGTGGGAGTA | 67057 |
| rs581172196 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93301524 | AAGACCTAAGATCCT[A/G]TGTCTTGGGGATGAC | 67057 |
| rs581240135 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93297764 | ACAGGGTTTCTCTGT[A/G]TAGCTATGGCTGTCC | 67057 |
| rs581250228 | snp | A/C | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93330283 | ACACCTCTCCAGCCT[A/C]TGTTTATGTGTGCGC | 67057 |
| rs581251292 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93327093 | TACTACTTAAGCTAC[A/G]TGTTCTGCCTGTGTG | 67057 |
| rs581251679 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93294232 | AGCACAAACTTCTCT[C/T]AACTCCACTGAGACA | 67057 |
| rs581373403 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93296711 | CAGAGAAACCCTGTC[C/T]CGAAAAACCAAAATG | 67057 |
| rs581377479 | snp | C/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93315773 | GGGGAGGAAGTGTGG[C/G]ATATGGAGAAGACAG | 67057 |
| rs581416941 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93327354 | CCACCCTTACCTCTA[C/T]CCTGGGGAGCACAAA | 67057 |
| rs581493941 | snp | A/C | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93297770 | TTTCTCTGTATAGCT[A/C]TGGCTGTCCTGGAAC | 67057 |
| rs581539687 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93289913 | TTCGACAGGTCCTTG[A/G]AGTGTCCTTTCAAGG | 67057 |
| rs581541543 | snp | C/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93311087 | CACTCTGTAGACCAG[C/G]ATGGCCTCGAACTCA | 67057 |
| rs581543848 | snp | C/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93336521 | CGCAGGCCGCGCCCG[C/G]CCCCGCGCCCCGCCC | 67057 |
| rs581620192 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93296681 | AGAGTGAGTTCCAGG[A/G]CAGCCAGGGCTACAC | 67057 |
| rs581658672 | snp | G/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93330550 | ATACAGTGGGTTTTT[G/T]GTTTTTTGTTTTTTG | 67057 |
| rs581729715 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93315723 | GGTCAGGTCGGGTGG[A/G]GGGTGGGGGCATCCA | 67057 |
| rs581758961 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93315318 | GGATCCAGCTCAAGG[A/G]GAGGTCCCAGGGCCT | 67057 |
| rs581804675 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93302164 | ACTGCTTCTCAGGCT[A/G]GGAAGCAGGTCAACT | 67057 |
| rs581857475 | snp | A/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93295947 | CTTCTTCCCTACTCC[A/T]CCCTTCCTCCCCAGA | 67057 |
| rs581926173 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93328430 | AATGGCCTACTCAGC[A/G]TGGGCCCTTCATGTT | 67057 |
| rs582078471 | snp | A/C | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93298798 | AACAAAAAAACAAAA[A/C]AAAACAAAACAAAAC | 67057 |
| rs582179672 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93296750 | AATGAATGAATGAAT[A/G]AATGATTTTACACTC | 67057 |
| rs582278019 | snp | A/G/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93330159 | TCTGTTTATGTGTGC[A/G/T]CATCTGTGTATACTG | 67057 |
| rs582317000 | snp | A/C | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93306214 | AATTCACTCTGTAGA[A/C]CAGGCTGGCCTCAAA | 67057 |
| rs582420736 | snp | A/C | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93330191 | ACACCTCTGCAGCCT[A/C]TGTTTATGTGTGCGC | 67057 |
| rs582451694 | snp | A/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93285720 | CAAAGTAACAAAATG[A/T]GTCATACTGAAGGTT | 67057 |
| rs582452575 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93309896 | AAGGTTATTTTACAC[A/G]CATGTCCAGAAAAAA | 67057 |
| rs582472004 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93333829 | TAAGTATACAGCGCG[C/T]GTGTGTACATACACG | 67057 |
| rs582531804 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93297432 | CCCTGGGCAGTTTCA[A/G]TAAGCAATGCTGAGA | 67057 |
| rs582540903 | snp | A/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93321327 | ATGTGGGTGCTGGAA[A/T]TCAAACCCTGGTCCT | 67057 |
| rs582571169 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93299743 | CACAGCGGCTGGGTG[C/T]TAGCTTCATTAGGTA | 67057 |
| rs582634929 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93296738 | AATGAATGAATGAAT[A/G]AATGAATGAATGAAT | 67057 |
| rs582773969 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93315740 | GGTGGGGGCATCCAC[A/G]TGGAGATGGGGTGGG | 67057 |
| rs582779748 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93314229 | TCCATAATTCAAAAG[A/G]CTGACATACAATGAC | 67057 |
| rs582780002 | snp | C/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93295902 | TACCCAGAGGTCAAG[C/G]CTGCAGACCAGTGCA | 67057 |
| rs582791810 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93318192 | GTCAGGCCACCGTGT[A/G]AATTTTTTTAAATTA | 67057 |
| rs582890603 | snp | A/C | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93307970 | TATAGAATTTTAATA[A/C]AATTTCCTGATTTTT | 67057 |
| rs582893001 | snp | A/C | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93286802 | GTCAGATCTCATTAC[A/C]GATGGTTATGAGCCA | 67057 |
| rs582896551 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93333925 | ACACGTATGTAAGTA[C/T]ACAGTACATGTGTGC | 67057 |
| rs582995307 | snp | A/C | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93289720 | GCGCGCTCCCCTGGG[A/C]GCTGGGATGCCTCTG | 67057 |
| rs583001589 | snp | A/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93334669 | ACTAAAAATTGGATC[A/T]ACTGGTTAAAAACAA | 67057 |
| rs583075097 | snp | G/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93296684 | GTGAGTTCCAGGGCA[G/T]CCAGGGCTACACAGA | 67057 |
| rs583133323 | snp | G/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93300050 | GAATTTTTGGTTTTT[G/T]TTTTTTTTTTTTTGG | 67057 |
| rs583143366 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93330234 | TGGACACCTCTGCAG[C/T]CTCTGTTTATGTGTG | 67057 |
| rs583246766 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93297568 | TTAGTTGAAAGAAAA[A/G]GACAGACTTTTCAAG | 67057 |
| rs583251091 | snp | A/C | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93324271 | AACCGCTACTTTAGC[A/C]CAGAGCGCTCCAGCA | 67057 |
| rs583431427 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93330251 | TCTGTTTATGTGTGC[A/G]CATCTGTGTATACTG | 67057 |
| rs583476894 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93310662 | CTCAGAAGTCCGCCT[A/G]CCTCTGCCTCCCGAG | 67057 |
| rs583486317 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93296633 | GGAGGCAGAGGCAGG[C/T]GGATTTCTGAGTTTG | 67057 |
| rs583497568 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93315426 | TGAAAGAGTCAGATG[C/T]AGATATTTGCACACA | 67057 |
| rs583528141 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93336170 | GCCGGCGACCCCCAT[A/G]GATAATTCATCCTCC | 67057 |
| rs583745067 | snp | G/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93289901 | GTCTGCAGGCAGTTC[G/T]ACAGGTCCTTGAAGT | 67057 |
| rs583785611 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93297469 | ACAGTTAAAGAAGAG[A/G]AAGCAGGAAGCAGGA | 67057 |
| rs583858514 | snp | C/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93296665 | GGCCAGCCTGGTCTA[C/G]AGAGTGAGTTCCAGG | 67057 |
| rs583862530 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93315589 | ACCACCAAACAGACA[A/G]AATACACCAGGTGAT | 67057 |
| rs583937842 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93319922 | TGCATCAACCAAAAC[C/T]GACTCCTCAGTATTC | 67057 |
| rs583998678 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93322677 | GTATAGATTTATTTC[C/T]CCTCCAAAAAAAAGT | 67057 |
| rs584106383 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93311109 | TCGAACTCAGAAATC[A/G]ACCTGCCCTGCCTCC | 67057 |
| rs584119131 | snp | C/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93336528 | CGCGCCCGGCCCCGC[C/G]CCCCGCCCCGCCCGG | 67057 |
| rs584135305 | snp | G/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93290372 | GGTACATAGTCTTTG[G/T]TAATAAATAAACCCA | 67057 |
| rs584149700 | snp | A/C | | | upstream-variant-2KB | Yaf2 | GRCm38.p3 | 15:93338779 | GTAGACCAGGCTGGC[A/C]TCGAACTCAGAAATC | 67057 |
| rs584214989 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93303237 | TTTTAAAATTCTTTT[C/T]TAAAATTTACTTTGT | 67057 |
| rs584221620 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93330694 | ACTCCAATAGGTATG[C/T]TAAAGAAGAAAAGGG | 67057 |
| rs584254141 | snp | A/C | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93305926 | CGCGCAACAGGCTCG[A/C]TAGATCTTCTCAGCT | 67057 |
| rs584358160 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93311148 | GGGACTAAAGGCGTA[C/T]GCCACCACGCCCGGC | 67057 |
| rs584467843 | snp | G/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93297998 | ACATGTTCCTTCTTG[G/T]CTGTGTGGGGCTGGA | 67057 |
| rs584470220 | snp | C/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93333165 | GTATGCTCAAGGTTA[C/G]CCTGAGATACAGGGC | 67057 |
| rs584480051 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93328433 | GGCCTACTCAGCATG[A/G]GCCCTTCATGTTAAA | 67057 |
| rs584688835 | snp | G/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93297767 | GGGTTTCTCTGTATA[G/T]CTATGGCTGTCCTGG | 67057 |
| rs584702239 | snp | A/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93315744 | GGGGCATCCACATGG[A/T]GATGGGGTGGGGTGG | 67057 |
| rs584702293 | snp | C/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93296705 | GCTACACAGAGAAAC[C/G]CTGTCCCGAAAAACC | 67057 |
| rs584703687 | snp | A/C | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93296719 | CCCTGTCCCGAAAAA[A/C]CAAAATGAATGAATG | 67057 |
| rs584706380 | snp | A/G/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93330297 | TCTGTTTATGTGTGC[A/G/T]CATCTGTGTATACTG | 67057 |
| rs584809314 | snp | C/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93313908 | TGAGACTGACTGACT[C/G]TCTCTCTCTCTCTCT | 67057 |
| rs584940873 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93297789 | CTGTCCTGGAACTCA[C/T]TTTGTAGACCAGGCT | 67057 |
| rs584948537 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93301739 | ACTGTGTTTAACCTT[A/G]ATTTACTTAAAATGT | 67057 |
| rs585040496 | snp | G/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93316233 | CAGAGACAGGGATAA[G/T]TCTAACCTGTAACTT | 67057 |
| rs585109620 | snp | A/C | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93294234 | CACAAACTTCTCTCA[A/C]CTCCACTGAGACAGG | 67057 |
| rs585213105 | snp | A/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93327594 | GGCATGTCTGTGGAG[A/T]ATTTTCTAACTGCTA | 67057 |
| rs585270949 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93295980 | CTGGCTGAACTGGCT[A/G]ACCTGGCTGAACTGG | 67057 |
| rs585309599 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93296742 | AATGAATGAATGAAT[A/G]AATGAATGAATGATT | 67057 |
| rs585381427 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93310572 | TTTTTTTGGTTTTTC[A/G]AGACAGGGTTTCTCT | 67057 |
| rs585396531 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93308062 | CAGTCTGACTGGCAC[A/G]CTTCTAGAATCCCCT | 67057 |
| rs585398865 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93287166 | CAAGAGAAAGCTAAG[C/T]ATCTGTAGTGCCACT | 67057 |
| rs585410364 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93333969 | GAAGAAAAGGCTTCA[A/G]ACATCTAGAATAGCT | 67057 |
| rs585580685 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93315410 | AGACCCAACAAGCAG[C/T]TGAAAGAGTCAGATG | 67057 |
| rs585603644 | snp | C/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93330184 | ATACTGGACACCTCT[C/G]CAGCCTCTGTTTATG | 67057 |
| rs585684396 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93289732 | GGGAGCTGGGATGCC[C/T]CTGCTGAGCAGGCTT | 67057 |
| rs585699083 | snp | C/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93336153 | GGCACGGCACGGCAG[C/G]GGCCGGCGACCCCCA | 67057 |
| rs585803314 | snp | A/C | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93296755 | ATGAATGAATGAATG[A/C]TTTTACACTCGAAGG | 67057 |
| rs585807705 | snp | G/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93320254 | TTTAAGCCGCTTTTT[G/T]GGGTAGACAAACAAA | 67057 |
| rs585830558 | snp | A/C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93297433 | CCTGGGCAGTTTCAG[A/C/T]AAGCAATGCTGAGAA | 67057 |
| rs585830716 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93333835 | TACAGCGCGTGTGTG[C/T]ACATACACGTATGTA | 67057 |
| rs585918132 | snp | A/C | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93298803 | AAAAACAAAACAAAA[A/C]AAAACAAAACAAAAA | 67057 |
| rs585920392 | snp | A/C | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93315439 | TGCAGATATTTGCAC[A/C]CAACCAATGGACAGA | 67057 |
| rs585935099 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93299872 | ACCAGAGCCCTGGCT[C/T]TCTTCTCCATCACAC | 67057 |
| rs586037982 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93322365 | CAACAGTCCATATTT[C/T]CTTCCATAAATTTTA | 67057 |
| rs586061159 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93296647 | GCGGATTTCTGAGTT[C/T]GAGGCCAGCCTGGTC | 67057 |
| rs586174642 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93323455 | TCACTTCCCTCTGCA[C/T]TGGCAGTGCATCACC | 67057 |
| rs586184755 | snp | A/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93290366 | GACTATGGTACATAG[A/T]CTTTGTTAATAAATA | 67057 |
| rs586211184 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93286183 | AACAGACATATAAAT[A/G]TCTTCTAAATATCTG | 67057 |
| rs586225051 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93306277 | TGCCTCCCAAGTGCT[A/G]GGGTTAAAGGTGTGC | 67057 |
| rs586269545 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93296694 | GGGCAGCCAGGGCTA[C/T]ACAGAGAAACCCTGT | 67057 |
| rs586281225 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93330205 | TCTGTTTATGTGTGC[A/G]CATCTGTGTATACTG | 67057 |
| rs586311853 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93295934 | CCTCACTTAGCATCT[C/T]CTTCCCTACTCCACC | 67057 |
| rs586317434 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93315295 | GGTCCAGCAACAGGC[C/T]CAAAGTGGGATCCAG | 67057 |
| rs586548975 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93297491 | GAAGCAGGACGAGCA[A/G]AGCTACCATGCCCAA | 67057 |
| rs586646737 | snp | G/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93300055 | TTTGGTTTTTTTTTT[G/T]TTTTTTTTGGAATGA | 67057 |
| rs586654142 | snp | A/C | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93330237 | ACACCTCTGCAGCCT[A/C]TGTTTATGTGTGCGC | 67057 |
| rs586670540 | snp | G/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93315742 | TGGGGGCATCCACAT[G/T]GAGATGGGGTGGGGT | 67057 |
| rs586751946 | snp | C/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93330276 | ATACTGGACACCTCT[C/G]CAGCCTCTGTTTATG | 67057 |
| rs586843671 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93297769 | GTTTCTCTGTATAGC[C/T]ATGGCTGTCCTGGAA | 67057 |
| rs586911434 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93297750 | GTCTGTTTTTCAAGA[C/T]AGGGTTTCTCTGTAT | 67057 |
| rs586915212 | snp | A/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93326894 | TCCTCCTCAGCCACG[A/T]AGGGAAGCCTGGCAA | 67057 |
| rs587156217 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93300890 | CATGTGTGTGCATAT[A/G]GACATGTGGATGCTT | 67057 |
| rs587269080 | snp | G/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93327181 | TTGTGACACCATTTG[G/T]GTTGCACTAGTTTCT | 67057 |
| rs587342972 | snp | A/C | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93289903 | CTGCAGGCAGTTCGA[A/C]AGGTCCTTGAAGTGT | 67057 |
| rs587353765 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93310961 | CCCCTTTTGTTATAC[A/G]ACGGACAGACATTTT | 67057 |
| rs587357089 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93336263 | CGCCCCACCGCGGCC[A/G]CCGCCTGGCTGGCCG | 67057 |
| rs587432199 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93296667 | CCAGCCTGGTCTACA[A/G]AGTGAGTTCCAGGGC | 67057 |
| rs587454263 | snp | G/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93330330 | CACCTCTATGTGTGC[G/T]CATCTGTGTATACTG | 67057 |
| rs587535015 | snp | A/C | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93315590 | CCACCAAACAGACAA[A/C]ATACACCAGGTGATA | 67057 |
| rs587543569 | snp | C/T | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93301794 | GCCTGTAAATGGTAA[C/T]CTGAGGGGTTACACA | 67057 |
| rs587576391 | snp | A/G | | | intron-variant | Yaf2 | GRCm38.p3 | 15:93311145 | GCTGGGACTAAAGGC[A/G]TATGCCACCACGCCC | 67057 |
| rs587577230 | snp | A/T | | | upstream-variant-2KB | Yaf2 | GRCm38.p3 | 15:93338631 | GGTGTTTCTCCTCCA[A/T]GTATGACTGCGTGCG | 67057 |