| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs3671371 | snp | A/G | 0.5 | 0 | intron-variant | Yaf2 | GRCm38.p3 | 15:93306706 | GCTGGGCACGGTGGC[A/G]CACACCTTTAACCCC | 67057 |
| rs3671912 | snp | A/C | 0.5 | 0 | intron-variant | Yaf2 | GRCm38.p3 | 15:93306783 | TGTTACACAGAGAAA[A/C]CTTGTCTTGAAAAAC | 67057 |
| rs3697863 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Yaf2 | GRCm38.p3 | 15:93302018 | CACCCACTGAGTCGT[C/T]CTAACTTCACAAGAT | 67057 |
| rs3699619 | snp | C/T | 0.5 | 0 | intron-variant | Yaf2 | GRCm38.p3 | 15:93302292 | AAGCTTGCTTAGCAG[C/T]TAAGCTTAATGGTAG | 67057 |
| rs3714847 | snp | C/T | 0.5 | 0 | intron-variant | Yaf2 | GRCm38.p3 | 15:93302524 | AAATGCTGCTGCCCA[C/T]CCCCCATCTCAGAAG | 67057 |
| rs13482716 | snp | A/G | 0.367309 | 0.220768 | synonymous-codon, nc-transcript-variant | Yaf2 | GRCm38.p3 | 15:93285448 | GGAGGACCTGGACAC[A/G]CCCCGCTCAGTGCTG | 67057 |
| rs31591954 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Yaf2 | GRCm38.p3 | 15:93304354 | AACTGGAGACAGATC[A/G]AAGAGGAGCAGAATA | 67057 |
| rs31619124 | snp | A/G | 0.5 | 0 | intron-variant | Yaf2 | GRCm38.p3 | 15:93320319 | TTTGCCTGTAATCCC[A/G]CACTCTTGAGGCCTA | 67057 |
| rs31627313 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Yaf2 | GRCm38.p3 | 15:93327881 | TACAGACAAACAACA[G/T]TGTTACCTAAGGATG | 67057 |
| rs31636651 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Yaf2 | GRCm38.p3 | 15:93287676 | ACAAAACCAAGCGTA[C/T]ATGTTTCCCTTCCTC | 67057 |
| rs31649525 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Yaf2 | GRCm38.p3 | 15:93301947 | GGTGCTTTCTTTCCA[C/T]AGAGAATCATCCAGA | 67057 |
| rs31679899 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Yaf2 | GRCm38.p3 | 15:93301118 | CTGGGATCACAAGTA[C/T]GCACTAGAAAGCCTG | 67057 |
| rs31682342 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Yaf2 | GRCm38.p3 | 15:93303304 | CACATGCATGCTGGC[A/G]CCATCTCACAGTTAT | 67057 |
| rs31699455 | snp | C/G | 0.5 | 0 | intron-variant | Yaf2 | GRCm38.p3 | 15:93286882 | GTGCTCTTACCCGCT[C/G]AGCCATCTCACCAGA | 67057 |
| rs31752349 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Yaf2 | GRCm38.p3 | 15:93301563 | ACCACACCGAGTTTA[C/T]ACAGTGCTGGAGATA | 67057 |
| rs31765995 | snp | C/G | 0.5 | 0 | upstream-variant-2KB | Yaf2 | Mm_Celera | 15:93337293 | GATCCGGTTTTAATT[C/G]CAGCGGCGTCCTCCT | 67057 |
| rs31766985 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Yaf2 | GRCm38.p3 | 15:93289766 | TCCAGAGATGTGCGA[C/T]TGCTGAGTTCCTGCG | 67057 |
| rs31776522 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Yaf2 | Mm_Celera | 15:93286765 | GTACACTGTAGCTGT[C/G]TTCAGACACACCAGA | 67057 |
| rs31778415 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Yaf2 | GRCm38.p3 | 15:93304563 | AGAGTAGTCAGGAAT[A/C]CACTAAGTTTAAGAC | 67057 |
| rs31821358 | snp | A/G | 0.5 | 0 | intron-variant | Yaf2 | GRCm38.p3 | 15:93300341 | TCACTTAGTCTCCAC[A/G]GCAACTTTGACTTAT | 67057 |
| rs31850379 | snp | A/G | 0.5 | 0 | intron-variant | Yaf2 | Mm_Celera | 15:93308909 | AAAATTAATAAATTG[A/G]AAAAAGTTTAAGATC | 67057 |
| rs31858329 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Yaf2 | GRCm38.p3 | 15:93287077 | TTTCTGTGTATCAGC[A/G]TTGTGGCTGAAGTAC | 67057 |
| rs31862953 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | Yaf2 | GRCm38.p3 | 15:93303877 | AAGGGAGAGCGCTCG[G/T]CGACGCTGCTGCAAC | 67057 |
| rs31868579 | snp | C/T | 0.42 | 0.183303 | intron-variant | Yaf2 | GRCm38.p3 | 15:93303591 | ACAAAGCTGGTGCTT[C/T]ATGAAGTAATGTGTA | 67057 |
| rs31888418 | snp | C/T | 0.5 | 0 | intron-variant | Yaf2 | GRCm38.p3 | 15:93295000 | GGGTGTCACTGGGTA[C/T]ACAACCATATCAGAG | 67057 |
| rs31898043 | snp | C/G | 0.432133 | 0.171253 | intron-variant | Yaf2 | GRCm38.p3 | 15:93299787 | CGTGACCCCACGTGG[C/G]AGTTAGAAAAGTGAG | 67057 |
| rs31938808 | snp | A/G | 0.5 | 0 | intron-variant | Yaf2 | Mm_Celera | 15:93308860 | CAGAACTCAGCCAGG[A/G]CTACACAAGACCCTA | 67057 |
| rs31939406 | snp | A/T | 0.5 | 0 | intron-variant | Yaf2 | Mm_Celera | 15:93287566 | CGGGATGGAGATATA[A/T]AATTAGTTTTATTGC | 67057 |
| rs31987001 | snp | C/G | 0.475309 | 0.108333 | intron-variant | Yaf2 | GRCm38.p3 | 15:93303914 | TGCAGAGGAGAAAGC[C/G]GGAGCCACACAGGAA | 67057 |
| rs32011052 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Yaf2 | GRCm38.p3 | 15:93301909 | CATGGATTCTGGGTG[C/G]AGGTCAGAGGACAAC | 67057 |
| rs32023760 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Yaf2 | GRCm38.p3 | 15:93303077 | GATGGCAGTAATGTG[A/G]TATGCTGGCAAACCG | 67057 |
| rs32051764 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Yaf2 | Mm_Celera | 15:93289591 | CCTGGACCGTCCAAA[A/T]AAATCTCTTTTATGA | 67057 |
| rs32053788 | snp | A/G | 0.5 | 0 | intron-variant | Yaf2 | Mm_Celera | 15:93322818 | CTTATTTAACTTATA[A/G]ATACAATGCACAGTT | 67057 |
| rs32053883 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Yaf2 | GRCm38.p3 | 15:93304423 | AAATGATCACTACTC[A/G]TGCCAGGATGGTAAT | 67057 |
| rs32069885 | snp | G/T | 0.484429 | 0.0868505 | intron-variant | Yaf2 | GRCm38.p3 | 15:93303127 | ATCGATGCCATGGTC[G/T]TATGATATAGTCCTT | 67057 |
| rs32127871 | snp | C/T | 0.5 | 0 | intron-variant | Yaf2 | Mm_Celera | 15:93308719 | AATGTATGTTTATCA[C/T]ATTAAATTGAATTTT | 67057 |
| rs32163585 | snp | C/G | 0.475309 | 0.108333 | intron-variant | Yaf2 | GRCm38.p3 | 15:93304517 | ATCTTCAGATGAATG[C/G]AAAATATAGAATAAG | 67057 |
| rs32168850 | snp | C/T | 0.5 | 0 | intron-variant | Yaf2 | GRCm38.p3 | 15:93303601 | TGCTTTATGAAGTAA[C/T]GTGTAACTAAACTGT | 67057 |
| rs32181290 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Yaf2 | GRCm38.p3 | 15:93292766 | GCTATCACCTCTGTA[C/T]CTTGTGTCCTTTATT | 67057 |
| rs32197829 | snp | A/C | 0.5 | 0 | intron-variant | Yaf2 | Mm_Celera | 15:93308705 | TTTACCATATTCTCA[A/C]TGTATGTTTATCATA | 67057 |
| rs32214483 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Yaf2 | GRCm38.p3 | 15:93303114 | TGGACAGATGGAAAT[C/T]GATGCCATGGTCGTA | 67057 |
| rs32215945 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Yaf2 | GRCm38.p3 | 15:93328522 | GTGAGTATATTCAAC[A/G]ACCTTCCCAGACCTG | 67057 |
| rs32228635 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Yaf2 | GRCm38.p3 | 15:93324751 | CACTCACATATTTGA[C/T]TGCTTTAGCTAACCC | 67057 |
| rs32232902 | snp | A/C | 0.456747 | 0.140554 | intron-variant | Yaf2 | GRCm38.p3 | 15:93303360 | TGTCTGTAATAAATA[A/C]CTCCACTAATGAACA | 67057 |
| rs32235579 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Yaf2 | Mm_Celera | 15:93301213 | ACGGAGCCGTCCCCC[C/G]TCCCCCCCTCTTAAT | 67057 |
| rs32256303 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Yaf2 | GRCm38.p3 | 15:93326837 | CAGGCAGGCGGCCTG[A/G]CCACAGCTCTGGATC | 67057 |
| rs32277567 | snp | A/G | 0.375 | 0.216506 | intron-variant | Yaf2 | GRCm38.p3 | 15:93288025 | AGGATGCAACCAAAA[A/G]ATGAGAAAACACTGC | 67057 |
| rs32338840 | snp | A/C | 0.5 | 0 | intron-variant | Yaf2 | Mm_Celera | 15:93308884 | GACCCTATCTCAAAA[A/C]CAAAAGATTAAAATT | 67057 |
| rs32360238 | snp | C/G/T | 0.5 | 0 | intron-variant | Yaf2 | GRCm38.p3 | 15:93293365 | ACCAGAATGCATTAA[C/G/T]ATGCATAAAGCTGTC | 67057 |
| rs32362307 | snp | C/T | 0.5 | 0 | intron-variant | Yaf2 | GRCm38.p3 | 15:93291908 | ATAAGGTATATTTTA[C/T]ATCATAAATCCATAA | 67057 |
| rs32379262 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Yaf2 | GRCm38.p3 | 15:93288496 | ACACCTATGGAAGTG[A/G]TCTGGAGGTGTTGCG | 67057 |
| rs32417074 | snp | C/G | 0.475309 | 0.108333 | intron-variant | Yaf2 | GRCm38.p3 | 15:93303709 | TTAGTCGTCCACTCA[C/G]CAGCACAGTATGTGT | 67057 |
| rs32421006 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Yaf2 | GRCm38.p3 | 15:93300855 | GTGTCCAGGTGCATA[C/T]GGACATGTGGATGCA | 67057 |
| rs32435765 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Yaf2 | GRCm38.p3 | 15:93301929 | CAGAGGACAACAGGA[A/G]TAGGTGCTTTCTTTC | 67057 |
| rs32440226 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Yaf2 | GRCm38.p3 | 15:93304549 | AAGAGGCTATCTCGA[A/G]AGTAGTCAGGAATCC | 67057 |
| rs32459161 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Yaf2 | GRCm38.p3 | 15:93287980 | TTTAAAAAATCTTTT[A/T]TACTTTCTTATAAAA | 67057 |
| rs32468394 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Yaf2 | GRCm38.p3 | 15:93292721 | GGGGCAAGCAGAACC[A/G]TAGAACTGGTGCTCC | 67057 |
| rs32469717 | snp | A/C/T | 0.484429 | 0.0868505 | intron-variant | Yaf2 | GRCm38.p3 | 15:93290318 | TTACCTGGGAGCAAC[A/C/T]CTCACTGAAGAAGCT | 67057 |
| rs32470583 | snp | C/T | 0.5 | 0 | intron-variant | Yaf2 | GRCm38.p3 | 15:93292903 | TAATCCCACATTAGG[C/T]TCAGGGAACACTGCA | 67057 |
| rs32471492 | snp | A/G | 0.5 | 0 | intron-variant | Yaf2 | GRCm38.p3 | 15:93296055 | TTAGGCTATAGGCAT[A/G]GACCACCATGACAGG | 67057 |
| rs32481161 | snp | G/T | 0.465374 | 0.126941 | intron-variant | Yaf2 | GRCm38.p3 | 15:93301609 | CCCACTATTTATACC[G/T]TAGAGCGAGCTGCCT | 67057 |
| rs32482277 | snp | A/G | 0.5 | 0 | intron-variant | Yaf2 | GRCm38.p3 | 15:93300938 | TGTGTGCACATGGAT[A/G]CATGTGTGTGCACAT | 67057 |
| rs32521636 | snp | G/T | 0.486111 | 0.0821678 | intron-variant | Yaf2 | GRCm38.p3 | 15:93303616 | TGTGTAACTAAACTG[G/T]GTACATGTCTGATTA | 67057 |
| rs32530954 | snp | C/G | 0.5 | 0 | intron-variant | Yaf2 | GRCm38.p3 | 15:93303582 | TCTAGCCTTACAAAG[C/G]TGGTGCTTTATGAAG | 67057 |
| rs36326237 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Yaf2 | Mm_Celera | 15:93290291 | CAGAGGACACATGTT[A/C]AGGAATAAGAGTTAC | 67057 |
| rs36328255 | snp | A/G | 0.375 | 0.216506 | intron-variant | Yaf2 | GRCm38.p3 | 15:93298047 | TGTACCTAGGTGCTT[A/G]CAATTTACAATGCTG | 67057 |
| rs36336974 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Yaf2 | Mm_Celera | 15:93290401 | CAGACTTTTAAGTAC[G/T]GGTAATTCACAAAAT | 67057 |
| rs36358218 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Yaf2 | Mm_Celera | 15:93286029 | AAAGCTAGGGCCAGG[C/T]AACTCTTTACTCCAC | 67057 |
| rs36359669 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Yaf2 | Mm_Celera | 15:93290988 | ATTATAGCTTTGCCA[C/T]GTTCATATACTGTGC | 67057 |
| rs36373234 | snp | A/C | 0.32 | 0.24 | utr-variant-3-prime, nc-transcript-variant | Yaf2 | Mm_Celera | 15:93285384 | CTAAGTGGAGCAAGA[A/C]CGGTTAGTGAGACTC | 67057 |
| rs36403936 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Yaf2 | Mm_Celera | 15:93301671 | AGTTTATTACTTGAG[C/T]CGATCATGCTGGAGA | 67057 |
| rs36420444 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Yaf2 | Mm_Celera | 15:93305319 | CATGACTGGCCCATT[A/C]AAGTCTTCCTTCCTG | 67057 |
| rs36441027 | snp | A/C/G | 0.46875 | 0.121031 | intron-variant | Yaf2 | GRCm38.p3 | 15:93307350 | GAATGGTGTAGCTTG[A/C/G]ATATGGCTAAGGATG | 67057 |
| rs36458962 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Yaf2 | Mm_Celera | 15:93329502 | GACAACACACGAATG[A/G]CAGACAGTACATGAA | 67057 |
| rs36465299 | snp | C/G | 0.244898 | 0.249948 | synonymous-codon, nc-transcript-variant | Yaf2 | Mm_Celera | 15:93285466 | CCGCTCAGTGCTGTC[C/G]GAGCTGCAGCTGCCC | 67057 |
| rs36486428 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Yaf2 | Mm_Celera | 15:93326111 | CAACAAATCAGAGTA[A/G]AGCCTCAAGTCCTAA | 67057 |
| rs36487196 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Yaf2 | Mm_Celera | 15:93297571 | GTTGAAAGAAAAAGA[C/T]AGACTTTTCAAGAGG | 67057 |
| rs36503695 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Yaf2 | Mm_Celera | 15:93305913 | GAGGCACTATACACG[C/T]GCAACAGGCTCGCTA | 67057 |
| rs36507065 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Yaf2 | Mm_Celera | 15:93295596 | ACTGCTGCTTTTATT[C/T]CTCACTTCTCTCCGT | 67057 |
| rs36507165 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Yaf2 | Mm_Celera | 15:93305887 | ACAGACTTAGTAACA[A/G]CAGTAATAGAGAGGC | 67057 |
| rs36510896 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Yaf2 | Mm_Celera | 15:93295623 | CCGTCCTTCAAAACA[G/T]CACCCAGTGAGCCTC | 67057 |
| rs36563326 | snp | C/T | 0.32 | 0.24 | intron-variant | Yaf2 | Mm_Celera | 15:93289770 | GAGATGTGCGATTGC[C/T]GAGTTCCTGCGTCTC | 67057 |
| rs36572774 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Yaf2 | Mm_Celera | 15:93297404 | TCTTGAAGAGAGGAT[G/T]TTTCAAGCTAGTCCC | 67057 |
| rs36601218 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Yaf2 | GRCm38.p3 | 15:93298755 | ATAAATGTGCAGGTA[A/G]AAGTAAAAGCAAGCC | 67057 |
| rs36608693 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Yaf2 | Mm_Celera | 15:93290324 | GGGAGCAACCCTCAC[A/T]GAAGAAGCTCAAGCA | 67057 |
| rs36627478 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Yaf2 | Mm_Celera | 15:93293282 | GGAACGTGGGAAACG[A/G]ATTTGCAGCAAGAAG | 67057 |
| rs36630236 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Yaf2 | Mm_Celera | 15:93297589 | ACTTTTCAAGAGGGC[C/T]GCTCTCGAGACCAGG | 67057 |
| rs36647203 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Yaf2 | Mm_Celera | 15:93288426 | CATGGACACAGGTCT[A/G]CGTGTGCCTTCTCAC | 67057 |
| rs36654209 | snp | G/T | 0.244898 | 0.249948 | utr-variant-3-prime, nc-transcript-variant | Yaf2 | Mm_Celera | 15:93284384 | ATTGAAGGTTGTATC[G/T]GGAACTAGAGTACTG | 67057 |
| rs36660477 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Yaf2 | Mm_Celera | 15:93290829 | ATGGAAAGAGAAAAC[A/G]GAAAGATATGGCATG | 67057 |
| rs36669296 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Yaf2 | Mm_Celera | 15:93307308 | CACCTCTGCTGCTCA[C/T]TGTCGGTTAGAACAA | 67057 |
| rs36695007 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Yaf2 | Mm_Celera | 15:93286930 | AAGACCAAGATATAT[A/G]CTCAGGCCATTAGAA | 67057 |
| rs36707536 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Yaf2 | Mm_Celera | 15:93293780 | CTCTCTTCCATTTGA[C/T]AAGAGCAATCTGCTG | 67057 |
| rs36711891 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Yaf2 | Mm_Celera | 15:93290746 | CAGCCACTTGCTACA[C/T]ATGGGTAAAGACACT | 67057 |
| rs36720690 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Yaf2 | Mm_Celera | 15:93291653 | CCCATGTAGGTTGTC[A/G]CCAAGCGAGTACCAT | 67057 |
| rs36728148 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Yaf2 | GRCm38.p3 | 15:93307283 | TCATTCAAGTCTCAG[C/T]TCTGAATCTCACCTC | 67057 |
| rs36740961 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Yaf2 | Mm_Celera | 15:93298241 | ATTGTTGTTTACAAG[C/T]GTGTGTTTGTATTCT | 67057 |
| rs36753771 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime, nc-transcript-variant | Yaf2 | Mm_Celera | 15:93285271 | GGCAAATTCGTATTT[C/T]GTGTAAAACTCAAAT | 67057 |
| rs36770232 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Yaf2 | Mm_Celera | 15:93304040 | GTCGCAGAGGAGGAG[A/C]GATTAAAGGACACCT | 67057 |
| rs36775393 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime, nc-transcript-variant | Yaf2 | Mm_Celera | 15:93284172 | AAGCAAATGGCTAGC[A/G]AAAACAAGAGAACCT | 67057 |