SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6193349 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159331443 | GAGAGATAAATGCAG[A/G]TGGGTATGACATAAG | 26374 |
rs6193771 | snp | A/G | 0.5 | 0 | intron-variant | Rfwd2 | Mm_Celera | 1:159331510 | TTGGAGGTGGTTTGG[A/G]GGTTCTTTGTTTGTT | 26374 |
rs6230679 | snp | C/T | 0.5 | 0 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159261616 | gtgtgtgcgcgcgcg[C/T]gcgtatncgtatgta | 26374 |
rs6230693 | snp | A/G | 0.5 | 0 | intron-variant | Rfwd2 | Mm_Celera | 1:159261623 | cgcgcgcgngcgtat[A/G]cgtatgtatgtgtgt | 26374 |
rs6231338 | snp | C/T | 0.5 | 0 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159261745 | CTAGGCTGTCTCAGC[C/T]TCCGCAGTGCTGGGA | 26374 |
rs6232293 | snp | A/G | 0.455 | 0.143091 | intron-variant | Rfwd2 | Mm_Celera | 1:159261889 | TACTTGTTGTTTTTC[A/G]TTAGTCCTTTTTTGA | 26374 |
rs6250322 | snp | G/T | 0.5 | 0 | intron-variant | Rfwd2 | Mm_Celera | 1:159335065 | TTACATATTAGAAAA[G/T]TGAAAGAAAAAATAG | 26374 |
rs6251817 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159335372 | GGCATTGTTGCGGTA[A/G]ATCTCCTCCCAAATA | 26374 |
rs6265187 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Rfwd2 | Mm_Celera | 1:159270058 | TAGCAGCCAGATGTT[C/T]ACAGCAATATTCTGT | 26374 |
rs6284011 | snp | C/T | 0.5 | 0 | intron-variant | Rfwd2 | Mm_Celera | 1:159237798 | AAATGAACTACATTT[C/T]ATTATATCTCTCTGA | 26374 |
rs6284510 | snp | A/T | 0.5 | 0 | intron-variant | Rfwd2 | Mm_Celera | 1:159237885 | TAGTTATTGGTACCA[A/T]AACAGTGCTATTCGT | 26374 |
rs6339193 | snp | A/C | 0.5 | 0 | intron-variant | Rfwd2 | Mm_Celera | 1:159241063 | atcactctgggttct[A/C]atagggncttcatta | 26374 |
rs6339197 | snp | G/T | 0.5 | 0 | intron-variant | Rfwd2 | Mm_Celera | 1:159241070 | tgggttctnataggg[G/T]cttcattaagttgga | 26374 |
rs6370963 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159248942 | TTTCACATGGTGAAA[A/T]GTTATCTTTATTGAG | 26374 |
rs6373412 | snp | C/T | 0.5 | 0 | intron-variant | Rfwd2 | Mm_Celera | 1:159276228 | CTTTGCACACTGACT[C/T]CTCAACCCCACACCT | 26374 |
rs6373437 | snp | G/T | 0.5 | 0 | intron-variant | Rfwd2 | Mm_Celera | 1:159276247 | AACCCCACACCTATG[G/T]AATTTTACTAATCCT | 26374 |
rs6395862 | snp | C/T | 0.5 | 0 | intron-variant | Rfwd2 | Mm_Celera | 1:159283385 | attctggattgtagt[C/T]attccagatagagtc | 26374 |
rs6395925 | snp | C/T | 0.5 | 0 | intron-variant | Rfwd2 | Mm_Celera | 1:159283428 | ggaagagcactacaG[C/T]CTGAAGCCCAATCCA | 26374 |
rs6395951 | snp | C/T | 0.5 | 0 | intron-variant | Rfwd2 | Mm_Celera | 1:159283448 | AGCCCAATCCACCTC[C/T]TCTCGCTGCTCATCT | 26374 |
rs6407858 | snp | C/T | 0.5 | 0 | intron-variant | Rfwd2 | Mm_Celera | 1:159244492 | AAATAAATGTTATAT[C/T]AGTTGTGTTGAAAGT | 26374 |
rs6409704 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159283615 | AAAGTGCTTCGTGTA[G/T]ATTTCTTATACAGAA | 26374 |
rs6409734 | snp | A/C | 0.5 | 0 | intron-variant | Rfwd2 | Mm_Celera | 1:159283639 | TACAGAATAGTAAAA[A/C]AGTGTGTGTGCCAGG | 26374 |
rs30459689 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159314560 | CACCTTGAGGAAGAT[A/G]CTATCTTTTTAAAAT | 26374 |
rs30464552 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Rfwd2 | Mm_Celera | 1:159269421 | TAGATTTTAGAAATA[A/G]CTTCATTTGACTATA | 26374 |
rs30472651 | snp | G/T | 0.401235 | 0.199068 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159281274 | GGGAGGTGGGGAGAG[G/T]CAGGCATATTGTTTA | 26374 |
rs30475791 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159238423 | CATAGATAAATGAAT[C/T]TTAGCTGGGTGTATA | 26374 |
rs30505375 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159255848 | AGTCTAAAAAACTAA[C/T]TAGTTTTACTCACTG | 26374 |
rs30542577 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159272430 | CTTTTTCCCACTCTC[A/C]GTGACACACATTCTT | 26374 |
rs30559774 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Rfwd2 | Mm_Celera | 1:159242732 | ATGTTTTGGTAAACG[C/T]CAAACTCTTGTCATG | 26374 |
rs30566467 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159303685 | AGTGGAATCTCAGGG[C/T]TGTTTAGATTTGCAC | 26374 |
rs30568518 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Rfwd2 | Mm_Celera | 1:159329457 | CTACACTGCATGTGT[A/G]ACTTTAAGTGAAGAA | 26374 |
rs30602182 | snp | C/T | 0.42 | 0.183303 | intron-variant | Rfwd2 | Mm_Celera | 1:159321168 | GGCAAGCAACGCAAT[C/T]CAATTGTACAACAAT | 26374 |
rs30602938 | snp | C/T | 0.32 | 0.24 | intron-variant | Rfwd2 | Mm_Celera | 1:159260461 | TGCATGCTAGGCAGG[C/T]GCTCTACCCGAGCTC | 26374 |
rs30603446 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159233104 | GAGTGCTTAAGGATA[A/G]AGATGGAGGTCCAGT | 26374 |
rs30606380 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159241179 | GGAAGTTACCAGAGT[A/T]GTTAGTGTCCTGAGC | 26374 |
rs30607177 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Rfwd2 | Mm_Celera | 1:159259116 | TGTAAAAACATCAAG[C/T]AATTGTGTGTACTAA | 26374 |
rs30609330 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159336532 | AAATGTCTCCCATTA[A/G]ACATTTGCCTAGACC | 26374 |
rs30660948 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Rfwd2 | Mm_Celera | 1:159285256 | CATGCGATCTCATGT[A/G]TATGATAGGATAAGA | 26374 |
rs30663386 | snp | A/G | 0.5 | 0 | intron-variant | Rfwd2 | Mm_Celera | 1:159252722 | ATTTAAAAGCATTTA[A/G]TTTAGTCTTCCCTTT | 26374 |
rs30693835 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159335757 | TTAACATCAAACATA[A/G]TTGTCCAGTAGGTAG | 26374 |
rs30705670 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rfwd2 | Mm_Celera | 1:159318624 | TTAGAAAAGACATAA[A/G]CCAAACCAAATTGTT | 26374 |
rs30708227 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159334211 | AGAGGTAGGCTATGG[A/G]TTTAGTGGAGCGTTT | 26374 |
rs30717010 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159286131 | AATCCTTTATCAAAT[G/T]TCTATAATAGTTTAT | 26374 |
rs30744819 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159268000 | AGGGAATCCTTGAGA[A/G]GTTTGATAAAAAGCT | 26374 |
rs30750944 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Rfwd2 | Mm_Celera | 1:159286391 | ACTGAATAATTTGCT[C/T]TGGAAGATGCAGATT | 26374 |
rs30761774 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Rfwd2 | Mm_Celera | 1:159253566 | AGATAATACGTGAAG[A/G]TAATTCTCTGCTCTT | 26374 |
rs30800756 | snp | A/C | 0.415225 | 0.187619 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159317790 | TCTTCATACATTTAC[A/C]TTTATTTCATTATGA | 26374 |
rs30801802 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159276757 | GACTATATGATTGAA[C/T]ACATAGAACCTGATA | 26374 |
rs30805967 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159267223 | AGTTCAGATTACTTA[C/T]AGAAATTCATTGGGA | 26374 |
rs30808693 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Rfwd2 | GRCm38.p3 | 1:159257197 | ACATTGTTGGTGGAC[A/G]TTCGAGTGGTTTTTA | 26374 |
rs30853589 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159253622 | AATCTGAGTTTTTCA[A/G]ATCCCTTTAGGAGCC | 26374 |
rs30931405 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Rfwd2 | Mm_Celera | 1:159243890 | TTGGTCAATTTGTAT[A/G]TGTAATTTAGGTTGC | 26374 |
rs30944623 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Rfwd2 | Mm_Celera | 1:159329686 | ACAGTAGCAACTAAA[A/G]AGGCATAGGAAATAT | 26374 |
rs30951884 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Rfwd2 | Mm_Celera | 1:159295045 | TGGAATTAAAGTAAG[C/T]GATAAAATAATCAGT | 26374 |
rs30980274 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Rfwd2 | Mm_Celera | 1:159241334 | AGTATTTCTTTTGTC[C/T]ATATTGGAAGTTGTG | 26374 |
rs30987837 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159310490 | GATTTAATGTATAGT[A/G]GTAATAGTGCCTAAC | 26374 |
rs30996612 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159334419 | TTCAAGCCACTGCGC[A/T]GAGAGGTAGAACAAT | 26374 |
rs31000308 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159304531 | CATGTTGGTGTTCCT[C/T]CTTCTTGATTTTCTT | 26374 |
rs31000988 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159323939 | GGTTCCCACCCCCAA[A/C]CTTTATGTGTGCTAT | 26374 |
rs31013660 | snp | C/T | 0.32 | 0.24 | intron-variant | Rfwd2 | Mm_Celera | 1:159260103 | TTTGCTAGTTTGATG[C/T]ATCATAATGAAACAC | 26374 |
rs31048982 | snp | C/G | 0.415225 | 0.187619 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159248077 | CTCACGATAATTAGA[C/G]TTATTTGTAGAGTGG | 26374 |
rs31052830 | snp | G/T | 0.49827 | 0.0293608 | intron-variant | Rfwd2 | Mm_Celera | 1:159288182 | TGTTTTTAGTTCTTT[G/T]GGAAAAGTTTAAAAT | 26374 |
rs31101439 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Rfwd2 | Mm_Celera | 1:159284852 | TTTCTCATTCCAGAA[C/T]GTTTTATCGTTCCAG | 26374 |
rs31112472 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159248088 | TAGAGTTATTTGTAG[A/T]GTGGATCATTTCATT | 26374 |
rs31154774 | snp | A/G | 0.32 | 0.24 | intron-variant | Rfwd2 | Mm_Celera | 1:159321891 | TATAGGCAGTCACCT[A/G]GGAGCTGAGCCTCTG | 26374 |
rs31157265 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Rfwd2 | Mm_Celera | 1:159262167 | TCTTGTGATTTATCT[A/G]TACTGATTTCTTTGC | 26374 |
rs31160783 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159238510 | GAGTCCCAGGCTAGC[A/G]TGGGCTACATAAAGA | 26374 |
rs31177156 | snp | A/T | 0.32 | 0.24 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159271150 | AAGCATATATAAACC[A/T]TCACAGGTGTCATGC | 26374 |
rs31189680 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159299543 | CCATCTACTTGATTT[C/T]AAAGAACGTACACCT | 26374 |
rs31196850 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159334135 | CACTTGACAGAAAAT[G/T]AACATCCAGAATATG | 26374 |
rs31198913 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159277255 | GAAATGCCTCTGAGG[A/C]CACCCTGGTCTATAC | 26374 |
rs31214457 | snp | A/C | 0.5 | 0 | intron-variant | Rfwd2 | Mm_Celera | 1:159289820 | CGGGAAAAAAAAAAA[A/C]AAAAAAACAAACTTC | 26374 |
rs31230448 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159271476 | AGATCAGTCTTAGTC[A/G]GTGATCTATTGCTGT | 26374 |
rs31232172 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Rfwd2 | Mm_Celera | 1:159258036 | ACATCCATGTATATA[C/T]GTGCTCATGCCCCTG | 26374 |
rs31257634 | snp | C/T | 0.42 | 0.183303 | intron-variant | Rfwd2 | Mm_Celera | 1:159274263 | TTGGAAATGCTTTTT[C/T]TATTGACTTATAATT | 26374 |
rs31258065 | snp | A/T | 0.426035 | 0.177515 | intron-variant | Rfwd2 | Mm_Celera | 1:159249106 | AATTTGGGACTCTGT[A/T]AAGTTAAGATAAAAA | 26374 |
rs31259858 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Rfwd2 | Mm_Celera | 1:159328147 | TATAAGTGTTTTTTT[A/T]AAATATAAATTCTTT | 26374 |
rs31265834 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159259856 | TGTGGTGATCTTCTG[C/T]CCTTTATTACCACTC | 26374 |
rs31284026 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159290747 | TTTGGAAGAGCAGTC[A/G]GTGCTCTTAACCACT | 26374 |
rs31287041 | snp | A/G | 0.5 | 0 | intron-variant | Rfwd2 | Mm_Celera | 1:159252854 | ACAGGGTTTCTCTGT[A/G]TAGCTCTGGCTGTCC | 26374 |
rs31311724 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159337316 | GCTTTCAGAATGCCA[C/T]GAATTTATCTATAGC | 26374 |
rs31311725 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159337248 | TCGGGAGCTGTTTAT[C/T]CTCACACATGTCCAG | 26374 |
rs31311726 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159337234 | TGGAAAGCAAATGCT[C/T]GGGAGCTGTTTATCC | 26374 |
rs31311727 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159337067 | TGCTTCTGTCCATTG[C/T]CCTCTTCATGTAGGC | 26374 |
rs31311728 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159337052 | TAAAAAGATTTTTCA[C/T]GCTTCTGTCCATTGT | 26374 |
rs31311729 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159336944 | CCACCCTACCAAGTG[C/T]TTCTCTTCAGAGTCT | 26374 |
rs31311730 | snp | G/T | 0.5 | 0 | intron-variant | Rfwd2 | Mm_Celera | 1:159336927 | TTCAGATTGCCATTT[G/T]TCCACCCTACCAAGT | 26374 |
rs31311731 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159336795 | GCTTGATGTGCTCAG[A/T]CTTAAGTTTCCTGCA | 26374 |
rs31311732 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159336681 | AAGTGTGGGTCTCCC[A/G]GTTTCAAAGGTGGTC | 26374 |
rs31311733 | snp | C/G | 0.459184 | 0.136902 | intron-variant | Rfwd2 | Mm_Celera | 1:159336382 | TGGAGGCTGCAATTG[C/G]TTGCTTGGTTGGATT | 26374 |
rs31312254 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Rfwd2 | Mm_Celera | 1:159249013 | AGTAATAGAAGTTGT[A/G]GTAGTAATAAGTATA | 26374 |
rs31312424 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Rfwd2 | Mm_Celera | 1:159313526 | GCATGCACCACCATA[A/G]CCCATCCTATAGTAT | 26374 |
rs31312425 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159312876 | TACAATAATTGACCA[A/G]GAGGGTAGCTTGTCA | 26374 |
rs31312426 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rfwd2 | Mm_Celera | 1:159312794 | TAATAATTCAGTGAA[C/T]TGCCTGCAGTGCTGA | 26374 |
rs31312427 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Rfwd2 | Mm_Celera | 1:159312660 | TCTCTCCCACACACC[A/G]CTCACATTCTAAAAA | 26374 |
rs31312428 | snp | C/G | 0.32 | 0.24 | intron-variant | Rfwd2 | Mm_Celera | 1:159312398 | ATTTATATATATGTT[C/G]TATGTAATATGTTTC | 26374 |
rs31312429 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159312346 | TCTTCTTGGTCTCCT[C/T]GGGTTATGGGTTATG | 26374 |
rs31312430 | snp | A/T | 0.459184 | 0.136902 | intron-variant | Rfwd2 | Mm_Celera | 1:159311935 | TGTTTTAAAATTTCC[A/T]CTCATAGCTGGGCGT | 26374 |
rs31312431 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Rfwd2 | Mm_Celera | 1:159311826 | TGCTTCATTCACTTT[C/T]TTCTAAGCACTGTTG | 26374 |
rs31312432 | snp | A/T | 0.345679 | 0.230967 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159311504 | CCTCCAGTCAGCCCC[A/T]CTCACTCAGTCCCTG | 26374 |
rs31312433 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159311446 | TCATCTGGCTATTGG[A/G]ATTTGAATTTAGGGC | 26374 |
rs31312554 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159336378 | TATTTGGAGGCTGCA[A/G]TTGCTTGCTTGGTTG | 26374 |
rs31312555 | snp | C/T | 0.32 | 0.24 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159335101 | AGCTTTCTTCTCATC[C/T]TGTTGCATTTTATAA | 26374 |
rs31312556 | snp | G/T | 0.345679 | 0.230967 | intron-variant | Rfwd2 | Mm_Celera | 1:159335004 | TTAATATTTGCATTT[G/T]AATTATGGAGTTTCC | 26374 |
rs31312557 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Rfwd2 | Mm_Celera | 1:159334904 | ATAAATCCTTAAGAA[A/G]CCATCTCCATCATCC | 26374 |
rs31312558 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159332587 | ACAACAGTTTCATGT[C/T]TACTTTCATGTTATC | 26374 |
rs31312559 | snp | C/T | 0.32 | 0.24 | intron-variant | Rfwd2 | Mm_Celera | 1:159332546 | TTTGTTGTCTCCCTG[C/T]CCCCGATTAGTTCCC | 26374 |
rs31312560 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159332460 | GCTATATGATGCCAC[A/T]TTTGTATAAGTATAA | 26374 |
rs31312561 | snp | A/G | 0.32 | 0.24 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159331369 | TGTGTATGTCATAAG[A/G]GATATACAACGGTAG | 26374 |
rs31312562 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159331275 | TCCCATAGTTAATAG[C/T]CCACACACTCTTGGA | 26374 |
rs31312563 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159330811 | CTAGATAAAAACCAG[C/T]TGTCTTTATCTTCTG | 26374 |
rs31313104 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Rfwd2 | Mm_Celera | 1:159284803 | ATAGACTTCTAGATA[G/T]CTTAAAGAATGCTGT | 26374 |
rs31313105 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Rfwd2 | Mm_Celera | 1:159284413 | ATTGGAAAGTATTAT[C/G]TGAGGATTGTAGTTT | 26374 |
rs31313106 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Rfwd2 | Mm_Celera | 1:159282400 | ACAGATGCCCTTAAT[C/G]ATGTTGAAGATGTTT | 26374 |
rs31313107 | snp | A/G/T | 0.401235 | 0.199068 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159281112 | GGTATCTTTATAAGG[A/G/T]ACATCTTAATTCTCA | 26374 |
rs31313108 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rfwd2 | Mm_Celera | 1:159280711 | AGATTTCAGTAGTCA[C/T]TTTCTTAATGTGTGT | 26374 |
rs31313109 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Rfwd2 | Mm_Celera | 1:159279590 | TACTTACTGTACACA[A/G]TCATCTATGGTATAC | 26374 |
rs31313110 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Rfwd2 | Mm_Celera | 1:159279417 | CTGTAGGTGAGAGAA[C/T]TAAATGTCTATTAAA | 26374 |
rs31313111 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Rfwd2 | Mm_Celera | 1:159278281 | GATCTTGTTTCTTGT[A/T]CATAACAGAAGTACT | 26374 |
rs31313112 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159277846 | TAAAGTCTGAAACCT[C/T]ACTAACCTATTTGGA | 26374 |
rs31313113 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Rfwd2 | Mm_Celera | 1:159277536 | AAGTAGACTAGGCTT[A/G]CTAGGACAGAGGAGA | 26374 |
rs31313384 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159310689 | GTCTGCCTTCATGCT[A/G]TCTGCTTTTTAAATA | 26374 |
rs31313385 | snp | A/G | 0.42 | 0.183303 | intron-variant | Rfwd2 | Mm_Celera | 1:159310394 | TTATTCTCAGAAGTG[A/G]AATTATTCTATCATA | 26374 |
rs31313386 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Rfwd2 | Mm_Celera | 1:159309105 | TCTGTTTTTCCATTT[A/G]AGTGAAGGAAAAATG | 26374 |
rs31313387 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159309045 | AAGTTGTTTATTGAA[A/G]CTCATGCAAGTCTTT | 26374 |
rs31313388 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Rfwd2 | Mm_Celera | 1:159308692 | CATATGTTATTTTTA[A/G]AATGTATCAAATACA | 26374 |
rs31313389 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159308644 | TACTTAAGATAATTG[A/T]GTTTGTACCAAATGC | 26374 |
rs31313390 | snp | C/T | 0.5 | 0 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159308269 | ATCAGAAAATCTAGA[C/T]ATTCCTAACATCTCT | 26374 |
rs31313391 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159308261 | TACTATCAATCAGAA[A/G]ATCTAGATATTCCTA | 26374 |
rs31313392 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159308199 | AGCTCTGTCTGTCAT[A/C]CTCTGTGATCTTAGT | 26374 |
rs31313393 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Rfwd2 | Mm_Celera | 1:159308086 | TTGGGGCTCAACAGT[C/T]TTTAATATCTGTCAT | 26374 |
rs31313404 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Rfwd2 | Mm_Celera | 1:159330754 | TTTAAAGGTGTGTGG[C/T]TTCCTATGTTATTTT | 26374 |
rs31313405 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159330660 | CCACTGTCTCTGGTC[A/G]ATAATACATACACTT | 26374 |
rs31313406 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159330642 | CACTGTGTTGAGGTA[A/T]ACCCACTGTCTCTGG | 26374 |
rs31313407 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159330580 | ATCGACATCCCTTGC[C/T]TCTACGTATACTCAA | 26374 |
rs31313408 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159330551 | AACACTTTAGTGGAC[C/T]AGGAGAACCACGAAT | 26374 |
rs31313409 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159330505 | AAAACTCTGTATCCT[A/G]GTTTCAGATTGATCC | 26374 |
rs31313410 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159330382 | GAGCCTTGGAACTTC[A/G]GGGAATGGAGATTTG | 26374 |
rs31313411 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Rfwd2 | Mm_Celera | 1:159330287 | TAAAATGTGAGAAAA[C/T]GAATAATTTTTTATG | 26374 |
rs31313412 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159330167 | TGATGTCAGCCTTTG[A/T]CCTCTTTACACTCCC | 26374 |
rs31313413 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rfwd2 | Mm_Celera | 1:159329941 | TGGAGAAGAGAAGAG[A/G]GGCCGTGTAGAGGGA | 26374 |
rs31313444 | snp | C/T | 0.32 | 0.24 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159256661 | CTGCTTTCTGGGGCT[C/T]AGTGCTAAGTCTATG | 26374 |
rs31313445 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159256623 | CTTTATGTAAGTGTG[C/T]TTGTACTGTATGAAC | 26374 |
rs31313446 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159256616 | TTTTAAGCTTTATGT[A/T]AGTGTGCTTGTACTG | 26374 |
rs31313447 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159256519 | GATTTCCTTCTTCCT[C/T]GCCTGCTTGCTAGCA | 26374 |
rs31313448 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159256433 | CTATAGAATAGAATA[A/G]CATGTACATAACTTT | 26374 |
rs31313449 | snp | A/G | 0.32 | 0.24 | intron-variant | Rfwd2 | Mm_Celera | 1:159256398 | AAATGAAACATGGAA[A/G]ATTGTATCTTAAGGT | 26374 |
rs31313450 | snp | G/T | 0.498615 | 0.0262793 | intron-variant | Rfwd2 | Mm_Celera | 1:159256035 | TAACACTTTAGCCAT[G/T]ACTGCTTTGTTTTAA | 26374 |
rs31313451 | snp | G/T | 0.401235 | 0.199068 | intron-variant | Rfwd2 | Mm_Celera | 1:159255574 | TCATTAAGCTTCTTG[G/T]GGCTCTTTAGTACTG | 26374 |
rs31313452 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Rfwd2 | Mm_Celera | 1:159255476 | TTTGGCAGGTCTTTT[C/T]TCGGGTAGCCGATAT | 26374 |
rs31313453 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rfwd2 | Mm_Celera | 1:159255120 | CCCATGAATGTAAAC[A/G]TCTGCTGCTGCAGCG | 26374 |
rs31313639 | snp | C/T | 0.408163 | 0.193609 | downstream-variant-500B | Rfwd2 | GRCm38.p3 | 1:159348032 | GAGTTTATTTTTTCA[C/T]CGATTGTATTATCCT | 26374 |
rs31313640 | snp | A/G | 0.408163 | 0.193609 | downstream-variant-500B | Rfwd2 | GRCm38.p3 | 1:159347917 | GGGAAAATAGTTGGA[A/G]GTTAATAGGAGCTTG | 26374 |
rs31313641 | snp | A/G | 0.408163 | 0.193609 | downstream-variant-500B | Rfwd2 | GRCm38.p3 | 1:159347897 | GAATGGTGGGATCTG[A/G]TCACGGGAAAATAGT | 26374 |
rs31313642 | snp | A/G | 0.408163 | 0.193609 | downstream-variant-500B | Rfwd2 | Mm_Celera | 1:159347836 | GAGGAGCCCAATACA[A/G]TGGCACTTTTAGCAC | 26374 |
rs31313643 | snp | G/T | 0.260355 | 0.249785 | downstream-variant-500B | Rfwd2 | GRCm38.p3 | 1:159347795 | AGCTTTTAGAAAGAA[G/T]AAAGAACACAGGATG | 26374 |
rs31314174 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159329894 | TTCTGTGGATGAGTT[A/C]ATGGAAGCTGAGGAG | 26374 |
rs31314175 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159329755 | ACAGAAACAGAATGA[C/T]GGCAGCTCTGGATTA | 26374 |
rs31314176 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159329714 | TATAAGACAAAATAA[C/G]TAGAAATTCAGCATA | 26374 |
rs31314177 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159329665 | TTAAAATACAGTAAG[C/T]AGGGCACAGTAGCAA | 26374 |
rs31314178 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Rfwd2 | Mm_Celera | 1:159329606 | TTAAATTATCTATAA[A/G]AGAAAATTAACATAC | 26374 |
rs31314179 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159329531 | GAAATCAACTTCAGA[G/T]CCTGTGAATCCCTGA | 26374 |
rs31314180 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159329513 | AGATAAACTGTCACA[C/T]TGGAAATCAACTTCA | 26374 |
rs31314181 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Rfwd2 | Mm_Celera | 1:159329109 | ATGCCATGCATCTTC[C/T]GTACCATATTTTAGC | 26374 |
rs31314182 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159329032 | ATGCTGAGCAGCTTT[C/T]AGTCTGGAAGGTTCT | 26374 |
rs31314183 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159328996 | ATGTAGCCCTTAACA[G/T]TCACTGCTGCACACT | 26374 |
rs31314284 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159277481 | TTGTAACCAAATGAA[A/G]AAACAGTGCAGGAAG | 26374 |
rs31314285 | snp | C/G | 0.495868 | 0.0452663 | intron-variant | Rfwd2 | Mm_Celera | 1:159277258 | ATGCCTCTGAGGCCA[C/G]CCTGGTCTATACACA | 26374 |
rs31314286 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Rfwd2 | Mm_Celera | 1:159276944 | TGAGAATCACCTGTT[C/T]AGAGTCAATTTATTT | 26374 |
rs31314287 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Rfwd2 | Mm_Celera | 1:159276093 | AAGTACTTAGGAATA[C/T]GGCACATTGTCCAAA | 26374 |
rs31314288 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159275597 | AGTCCTGAGAATTTT[G/T]CTGTAAATAATGAAA | 26374 |
rs31314289 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159275395 | GAGCTATGATAGCAC[A/T]CTTGAAGTCAGGAGA | 26374 |
rs31314290 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159275063 | CTGATATCTTAATCC[G/T]GGTATTCTTACTTTG | 26374 |
rs31314291 | snp | C/T | 0.32 | 0.24 | intron-variant | Rfwd2 | Mm_Celera | 1:159274798 | AACTAAACACTTCCT[C/T]ATCTTGTGCATGTTA | 26374 |
rs31314292 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159274764 | ATACTAGGTTCCCTA[C/T]TCAGCATATGTATTA | 26374 |
rs31314293 | snp | C/T | 0.32 | 0.24 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159274706 | TTTCTTTTTCAGCTT[C/T]AGGATTATTGTAGAA | 26374 |
rs31314314 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Rfwd2 | Mm_Celera | 1:159307828 | TTTTCTTAGTGCTTT[A/T]TTCGGTAATCCACAC | 26374 |
rs31314315 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Rfwd2 | Mm_Celera | 1:159307818 | TGTTAACTGCTTTTC[C/T]TAGTGCTTTATTCGG | 26374 |
rs31314316 | snp | C/T | 0.32 | 0.24 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159307548 | AAATGCCTGAAATTG[C/T]TCAAGGCCAAAACCT | 26374 |
rs31314317 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159307332 | CTTTGTACATATTTA[C/T]AGCATATAGCCATTG | 26374 |
rs31314318 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159307311 | GAGTCTGTGCTCTTT[A/C]AATCCCTTTGTACAT | 26374 |
rs31314319 | snp | C/T | 0.152778 | 0.230321 | synonymous-codon | Rfwd2 | Mm_Celera | 1:159306675 | GGATGCAGTGGATAT[C/T]CATTACCCTGAGAAT | 26374 |
rs31314320 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159306540 | TGGATACATAGCCTC[A/G]TAGATGACATGTGTG | 26374 |
rs31314321 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159306506 | TGCAGAAAATTTGCT[A/G]TAGATAATATCACAG | 26374 |
rs31314322 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159306494 | AAAAAAGTAAAATGC[A/T]GAAAATTTGCTGTAG | 26374 |
rs31314323 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Rfwd2 | Mm_Celera | 1:159306179 | TTTCCATACTAGGAT[A/G]TAATATGGTTATTAA | 26374 |
rs31314424 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Rfwd2 | Mm_Celera | 1:159253257 | ATATAAGGAAAGTCC[C/T]GTGAATCCCAGCCTC | 26374 |
rs31314425 | snp | A/C | 0.415225 | 0.187619 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159253190 | CAGTTTAATACTACA[A/C]AGTTTTCAGTGGGTC | 26374 |
rs31314426 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Rfwd2 | Mm_Celera | 1:159252976 | CTGCCTGGCTTTGGT[G/T]TTCTTTTCTTAAGCT | 26374 |
rs31314427 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Rfwd2 | Mm_Celera | 1:159252647 | CTTATGTTTAGTTTT[C/T]GTTATTTCTTGTATC | 26374 |
rs31314428 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Rfwd2 | Mm_Celera | 1:159252435 | AGCAGATGGGAAAAC[A/G]TATAGAAGTAGTACA | 26374 |
rs31314429 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159251145 | GTGCACAGAGCTGAG[A/G]GACTATTTCCTTGAG | 26374 |
rs31314430 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159250555 | AAACATGCAAATCCT[C/G]TCCATGCGTCTCAGG | 26374 |
rs31314431 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Rfwd2 | Mm_Celera | 1:159250416 | GTTATATATTGTAGA[A/G]CAGAGGCTCTGGGAT | 26374 |
rs31314432 | snp | A/T | 0.49827 | 0.0293608 | intron-variant | Rfwd2 | Mm_Celera | 1:159249967 | TTTAGAATCTAAAGC[A/T]GTCTTGTTAAGTTGC | 26374 |
rs31314433 | snp | A/C | 0.415225 | 0.187619 | intron-variant | Rfwd2 | Mm_Celera | 1:159249793 | TAGAAATGTCAACTT[A/C]GTATTTGTCTTCTGT | 26374 |
rs31314474 | snp | A/G | 0.408163 | 0.193609 | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159347083 | TATCAAAGGGATATG[A/G]CTTTTTAGAAATAAA | 26374 |
rs31314475 | snp | A/C | 0.408163 | 0.193609 | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159346540 | AACTTCTTACATTTA[A/C]AACTTGCTAAACTTA | 26374 |
rs31314476 | snp | A/G | 0.408163 | 0.193609 | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159346431 | ACTTAGGAAAGAGGA[A/G]AAATAATTATACAAT | 26374 |
rs31314477 | snp | A/T | 0.336735 | 0.234472 | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159346393 | CATAGTCACATTCCA[A/T]GAGGCTGGTTAGAAA | 26374 |
rs31314478 | snp | A/G | 0.48 | 0.0979796 | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159346328 | ACAGCAATCCCAACA[A/G]AACTAAAGCAATGGT | 26374 |
rs31314479 | snp | A/G | 0.489796 | 0.070696 | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159346275 | GTTTTAAACTCTTTA[A/G]ACTACCAGAAAGTCA | 26374 |
rs31314480 | snp | A/G | 0.408163 | 0.193609 | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159346247 | AAATTATTGAAGCCA[A/G]TTGTCTTTTGAGGTT | 26374 |
rs31314481 | snp | C/T | 0.408163 | 0.193609 | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159346215 | ATACCTAAGTAAGCT[C/T]ACATTTTTTTGAACT | 26374 |
rs31314482 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159346189 | GTGGATCCCTCAGCT[A/G]AAGGTTACTGATACC | 26374 |
rs31314483 | snp | G/T | 0.489796 | 0.070696 | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159346064 | TTGGGTCACGCAAAA[G/T]TAATGTGGATAATAC | 26374 |
rs31315094 | snp | A/G | 0.152778 | 0.230321 | synonymous-codon | Rfwd2 | Mm_Celera | 1:159328690 | CGTTAAGAGTGTATT[A/G]GACAAAGATCGGAAA | 26374 |
rs31315095 | snp | A/C | 0.444444 | 0.157135 | synonymous-codon | Rfwd2 | Mm_Celera | 1:159328675 | TTTTAAGTTTGATAC[A/C]GTTAAGAGTGTATTA | 26374 |
rs31315096 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159328287 | TAATCTTGTCTTTCA[A/G]ATGTGAATATAAAAG | 26374 |
rs31315097 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Rfwd2 | Mm_Celera | 1:159328259 | TCCTGTAGTTCGCAA[C/T]TAATTGGTCTTATAA | 26374 |
rs31315098 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159328252 | CCTTTTCTCCTGTAG[C/T]TCGCAACTAATTGGT | 26374 |
rs31315099 | snp | A/C/G | 0.408163 | 0.193609 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159327793 | GTGTCAGCTTGACTT[A/C/G]TCATCTGATAGGGTA | 26374 |
rs31315100 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Rfwd2 | Mm_Celera | 1:159327533 | TCCTTTTGATGTAGC[A/G]GTCGTTTGACTTGCA | 26374 |
rs31315101 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Rfwd2 | Mm_Celera | 1:159327515 | ATTTTACCCTCTCTA[A/G]TGTCCTTTTGATGTA | 26374 |
rs31315102 | snp | G/T | 0.18 | 0.24 | intron-variant | Rfwd2 | Mm_Celera | 1:159327430 | TTTAGATATGCCACA[G/T]TTTCTGTAGAAACTA | 26374 |
rs31315103 | snp | A/T | 0.33241 | 0.236027 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159327395 | AGACTTGCCAAAGAT[A/T]TTCACTGCCCTCTTG | 26374 |
rs31315154 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159305975 | AAAAAGGGATATGCC[A/G]TGACTTTTTGTAATT | 26374 |
rs31315155 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159305767 | TTTCACCTGCATTAG[A/G]CAATTTAGATTTCTG | 26374 |
rs31315156 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159305000 | GGTGTTTCTAAATTA[C/T]CTGAGTTAAAGATCA | 26374 |
rs31315157 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159304973 | TATAACTGATTCTTA[C/T]TTGAGTTACTAGGTG | 26374 |
rs31315158 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159301212 | AATGTGAAAGAAAAT[A/G]CAATCTCCACGTTGT | 26374 |
rs31315159 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159300962 | TGCATAAACATATAA[C/T]AGACTGTGAGACTAG | 26374 |
rs31315160 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159300721 | TTTTAACTGACTTTG[C/T]CTGTGTTTGCACTCT | 26374 |
rs31315161 | snp | C/G | 0.5 | 0 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159300463 | CAGCCCATTTATTCT[C/G]ATTAAAATAGTAGTT | 26374 |
rs31315162 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Rfwd2 | Mm_Celera | 1:159300362 | TCCTTTAATTTGTTT[C/T]CCAGGTTTAATTTTT | 26374 |
rs31315163 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Rfwd2 | Mm_Celera | 1:159299859 | TCCTTCTTTAAAATG[A/G]ATTATAGTGAACAAA | 26374 |
rs31315324 | snp | A/G/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159274658 | ACATCTGCTAGCCCC[A/G/T]ACTTTCTGCTAAAGG | 26374 |
rs31315325 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Rfwd2 | Mm_Celera | 1:159274573 | TACCAAGAAAAATGG[A/T]TTACTTTAAAAGGAA | 26374 |
rs31315326 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159274437 | CTAGTTCTCTTGACT[A/T]GTTGTTATTGGAGGC | 26374 |
rs31315327 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Rfwd2 | Mm_Celera | 1:159274207 | AAGCACCATCATTTT[C/T]TTTATTCCCATAATC | 26374 |
rs31315328 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159274158 | AAAGAAAATTTCTCT[C/T]GCTGTTTCCATCTCC | 26374 |
rs31315329 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159273975 | AAATGGAATGCAGTA[C/G]TGGCTATACTATGAT | 26374 |
rs31315330 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Rfwd2 | Mm_Celera | 1:159273871 | TTTTATAGTTTATTA[C/T]GTCTTTTAAGTGTTT | 26374 |
rs31315331 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159273853 | TGTTGAAATTAGAAG[G/T]TATTTTATAGTTTAT | 26374 |
rs31315332 | snp | A/T | 0.486111 | 0.0821678 | intron-variant | Rfwd2 | Mm_Celera | 1:159273798 | CATTTATTTTAGTCA[A/T]TACCTTGACAATACC | 26374 |
rs31315333 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rfwd2 | Mm_Celera | 1:159273066 | TCAGCAGTGCTAACG[C/T]ACAGTTTCATTCTAA | 26374 |
rs31315414 | snp | C/G | 0.277778 | 0.248452 | utr-variant-3-prime | Rfwd2 | GRCm38.p3 | 1:159346002 | CAAACCGTGTGACCT[C/G]TTAAATTGTCTAGTT | 26374 |
rs31315415 | snp | A/G | 0.277778 | 0.248452 | utr-variant-3-prime | Rfwd2 | GRCm38.p3 | 1:159345993 | CCAAGTTTCCAAACC[A/G]TGTGACCTCTTAAAT | 26374 |
rs31315416 | snp | A/T | 0.35503 | 0.226867 | utr-variant-3-prime | Rfwd2 | GRCm38.p3 | 1:159345732 | ACTGGCCAAGACTGA[A/T]CACTGACTGAGAAGA | 26374 |
rs31315417 | snp | A/G | 0.408163 | 0.193609 | utr-variant-3-prime | Rfwd2 | GRCm38.p3 | 1:159345717 | GAATCCCTCAGTTAT[A/G]CTGGCCAAGACTGAT | 26374 |
rs31315418 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime | Rfwd2 | GRCm38.p3 | 1:159345646 | CTAAGAGTTTGACTT[A/G]AGATCAAGTAAACAG | 26374 |
rs31315419 | snp | C/G | 0.132653 | 0.220748 | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159345613 | ATGATCACCATCAGA[C/G]CTTATCTGGTCAGAG | 26374 |
rs31315420 | snp | A/G | 0.408163 | 0.193609 | utr-variant-3-prime | Rfwd2 | GRCm38.p3 | 1:159345597 | TCTATACCCTGATTA[A/G]ATGATCACCATCAGA | 26374 |
rs31315421 | snp | C/T | 0.408163 | 0.193609 | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159345485 | TTGTGTTTCTCAACC[C/T]TTTTGGAATATCAAC | 26374 |
rs31315434 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rfwd2 | Mm_Celera | 1:159249600 | TTTACAGGGTCTGGT[A/G]GTATCACCATAGATA | 26374 |
rs31315435 | snp | C/T | 0.32 | 0.24 | intron-variant | Rfwd2 | Mm_Celera | 1:159249446 | ATGTTTTTATTTCAA[C/T]AATAGATATTAATAC | 26374 |
rs31315436 | snp | G/T | 0.46281 | 0.131194 | intron-variant | Rfwd2 | Mm_Celera | 1:159249101 | CTTTAAATTTGGGAC[G/T]CTGTAAAGTTAAGAT | 26374 |
rs31315437 | snp | A/T | 0.304688 | 0.243945 | intron-variant | Rfwd2 | Mm_Celera | 1:159248974 | AACATAAAAGATGGG[A/T]GTGTATTATAAAGAA | 26374 |
rs31315438 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Rfwd2 | Mm_Celera | 1:159248857 | TGTGTAATTATCAGC[A/G]TCCTTCAAGGTATTT | 26374 |
rs31315439 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159248803 | TGATGTCTGAGATTT[A/G]GAAAAATAATCATAT | 26374 |
rs31315440 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Rfwd2 | Mm_Celera | 1:159248734 | GATTGGCTAGTTTGG[A/C]TTAGATTACTCACAT | 26374 |
rs31315441 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Rfwd2 | Mm_Celera | 1:159248716 | AATTACTGGCAAAGA[A/C]CAGATTGGCTAGTTT | 26374 |
rs31315442 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Rfwd2 | Mm_Celera | 1:159248570 | TGGCTAAGACTGTTT[C/G]AGGGCTGTACATGGC | 26374 |
rs31315443 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Rfwd2 | Mm_Celera | 1:159248454 | GTTTGCATAGCTACC[C/T]TAGAACTTCAAAATG | 26374 |
rs31316034 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159299755 | GGGCCTCCTAGTATT[A/C]AAATTGGGGCTTTGT | 26374 |
rs31316035 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159299470 | ATACATCAGAGTGAT[C/T]GCCAAGGATTATTAC | 26374 |
rs31316036 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159299418 | ACAGTTGAATTTTTT[A/C/T]ATAACCACTGCAAAG | 26374 |
rs31316037 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159298917 | AATAAGGAAGAGAAA[A/G]TGGGTATAATGTTAA | 26374 |
rs31316038 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Rfwd2 | Mm_Celera | 1:159298748 | AAAACTGAAGAAATT[C/T]TAAGAATGTATGGCT | 26374 |
rs31316039 | snp | G/T | 0.46281 | 0.131194 | intron-variant | Rfwd2 | Mm_Celera | 1:159298667 | GATCTTTGGCTAGAT[G/T]ATATTATTAGAATAA | 26374 |
rs31316040 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159298434 | TTGAATATGAGGGAG[A/G]CAAATTGTGGTAGGT | 26374 |
rs31316041 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159297969 | GAAAACCTATCACCA[A/G]GAAATTGTAAAACTT | 26374 |
rs31316042 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Rfwd2 | Mm_Celera | 1:159297901 | ATAAAGACCAGAGAC[A/T]GTATTCTCAGATCAT | 26374 |
rs31316043 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159297731 | TAACTGTTTGAGACA[C/T]TGAATCAGATCAGTT | 26374 |
rs31316074 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159327357 | AATTAGTTTTCATTT[C/T]TGCAGATGAGCCCTG | 26374 |
rs31316075 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159327326 | TGTTCTTTTCTTTTC[C/T]AGCCATACTGGGGAG | 26374 |
rs31316076 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159327263 | AGCAGTGTTCACTGC[A/G]GTCTGTGCACTGGGA | 26374 |
rs31316077 | snp | C/G | 0.432133 | 0.171253 | intron-variant | Rfwd2 | Mm_Celera | 1:159326794 | GATGCTGGGATTGGA[C/G]CCATTAATGCTTGCT | 26374 |
rs31316078 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159326745 | AGACACATCTCTCAG[A/G]GCAAAGTCTAATTAT | 26374 |
rs31316079 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Rfwd2 | Mm_Celera | 1:159326560 | AGAGGTTGTTTTGGG[G/T]AAGCAACTAGATTTA | 26374 |
rs31316080 | snp | A/G | 0.32 | 0.24 | intron-variant | Rfwd2 | Mm_Celera | 1:159326352 | GGTAAAACCTGTATC[A/G]AAGTGTCCTATTCAG | 26374 |
rs31316081 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159325958 | TGTAGTACATTGTAA[A/G]AGGAAACATAAGAGA | 26374 |
rs31316082 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Rfwd2 | Mm_Celera | 1:159325499 | AGTGTGTCTGCTTCT[C/T]CCCAGCAAATGTCCC | 26374 |
rs31316083 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159325496 | TTAAGTGTGTCTGCT[G/T]CTTCCCAGCAAATGT | 26374 |
rs31316254 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Rfwd2 | Mm_Celera | 1:159344733 | GGTATTTGTGTTTGG[C/T]TTTTCAGTAGTACAT | 26374 |
rs31316255 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Rfwd2 | Mm_Celera | 1:159344650 | CTAATTTTTCATACA[A/G]TGCTTTAATTGAAAG | 26374 |
rs31316256 | snp | A/C | 0.426035 | 0.177515 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159344444 | CTGATAACGTCTAAA[A/C]CCTGGGTCACTAGGT | 26374 |
rs31316257 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159344438 | ATAACACTGATAACG[G/T]CTAAACCCTGGGTCA | 26374 |
rs31316258 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Rfwd2 | Mm_Celera | 1:159344405 | GTGGTTAGCACTGAA[G/T]TTGAAACACAAGAAA | 26374 |
rs31316259 | snp | C/T | 0.42 | 0.183303 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159344304 | CCTTTATTACTCATT[C/T]CCATCTTTGCTTTTC | 26374 |
rs31316260 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159344238 | TGACCTAAAATTACA[A/G]TGTCCATGAAACAAT | 26374 |
rs31316261 | snp | A/G | 0.5 | 0 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159344078 | CTATGGTGGAATCCC[A/G]TAGATTCTCAGAAGG | 26374 |
rs31316262 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Rfwd2 | Mm_Celera | 1:159343854 | AATAATGCCAACTTA[C/T]ATGAAAACTAGGCCT | 26374 |
rs31316263 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rfwd2 | Mm_Celera | 1:159343786 | CATGTGACAGGAACT[A/G]CAGTGTTAGCGAGGC | 26374 |
rs31316324 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159272958 | TTCCTGTGACTGTCT[A/G]CTAGGCACTTAAAGG | 26374 |
rs31316325 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159272897 | AGGGAAAGAGCATAT[C/G]GGGACAGCTTGTGTT | 26374 |
rs31316326 | snp | C/G | 0.459184 | 0.136902 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159272855 | CCGTCCCTCTTTTAG[C/G]TATATTAATGCTATA | 26374 |
rs31316327 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Rfwd2 | Mm_Celera | 1:159272823 | AACTATAAAGTGTCT[A/T]TAAGAGAGGAACAAC | 26374 |
rs31316328 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159272778 | GCTGAAGTTGCCTGT[A/G]CTGTGTGTGATTGCT | 26374 |
rs31316329 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159272747 | CTATGCTTTTTTCCC[C/T]CTAACATAAACAGAT | 26374 |
rs31316330 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159272624 | AGCAATTAAGAGAAG[A/T]CCCCCGAAGTTTAAA | 26374 |
rs31316331 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Rfwd2 | Mm_Celera | 1:159272571 | AAACTCTGTCTCTAC[C/T]CAGCCTTGAAAATAA | 26374 |
rs31316332 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Rfwd2 | Mm_Celera | 1:159271426 | AGAAAGCTAACTTCA[C/T]TGGTAAGTTCCACGT | 26374 |
rs31316333 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159271400 | CATAAAATAGAACAT[C/T]TTCAGATTATAGAAA | 26374 |
rs31316424 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Rfwd2 | Mm_Celera | 1:159248416 | ATAATGTTAAAATTC[C/T]TTTATGAGCATACAC | 26374 |
rs31316425 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Rfwd2 | Mm_Celera | 1:159248192 | CATTTCATCTTGCAT[A/G]CTATCTCTGTCTTGT | 26374 |
rs31316426 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Rfwd2 | Mm_Celera | 1:159248164 | ATTTATTTTTAAAGT[A/G]GATGATAATTGGCAT | 26374 |
rs31316427 | snp | A/T | 0.415225 | 0.187619 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159248037 | GTTACTCCATTATAT[A/T]ACAACTACTACATCA | 26374 |
rs31316428 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rfwd2 | Mm_Celera | 1:159247986 | TGGCCTTCATATGGC[C/T]TGTGTATTTGTAAGT | 26374 |
rs31316429 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Rfwd2 | Mm_Celera | 1:159247824 | TATTTCTACTCTTAA[C/T]ATTTAACCCTGTTAA | 26374 |
rs31316430 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Rfwd2 | Mm_Celera | 1:159247783 | TTAAATGTTTTCTAC[C/T]TTTTAGAATCAGACT | 26374 |
rs31316431 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Rfwd2 | Mm_Celera | 1:159247764 | GTAGATTGTAATAAT[A/T]TTGTTAAATGTTTTC | 26374 |
rs31316432 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159247716 | TTTTTACTTGTTCAT[C/T]CTTGATGTATTATTT | 26374 |
rs31316433 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159247326 | ATTAACTTTTATTTT[C/T]ATTTTAACCTTCATT | 26374 |
rs31316964 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rfwd2 | Mm_Celera | 1:159325331 | GCAATAGAGAGAAAA[A/G]ATAACTTATTTGAGT | 26374 |
rs31316965 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rfwd2 | Mm_Celera | 1:159325319 | GTAATATTTGGTGCA[A/G]TAGAGAGAAAAAATA | 26374 |
rs31316966 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Rfwd2 | Mm_Celera | 1:159325284 | CAAATTTGGTTTCTG[G/T]CACTACTTGTCCTGA | 26374 |
rs31316967 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159324575 | GGTGTATTGCATCTT[C/T]ATGTTCTGGTACTAG | 26374 |
rs31316968 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159324516 | ACCCATAGTTTAATT[G/T]CATGAGCACTGGCTT | 26374 |
rs31316969 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rfwd2 | Mm_Celera | 1:159324397 | TAGCCTGATAATGTG[C/T]AGTTTTCCTTTAGCC | 26374 |
rs31316970 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159324382 | AGATCTGGGTTTCAG[C/T]AGCCTGATAATGTGT | 26374 |
rs31316971 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Rfwd2 | Mm_Celera | 1:159324340 | GAGTTCAGAATATGG[G/T]TTTCTCCATGATAAA | 26374 |
rs31316972 | snp | C/G/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159324212 | GTTGTGGCCTGTCTG[C/G/T]TGCTCTGGTATTGGT | 26374 |
rs31316973 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159324033 | CTAACTATGGTGGGC[C/T]CAGCTTTTCCTCAGC | 26374 |
rs31317074 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159343749 | CAAAGCAGAACTGCA[G/T]TGTTAGCGAGGCACA | 26374 |
rs31317075 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159343660 | GCCACAGCTTTCTTT[A/T]ATTTGTAAGTGCCCA | 26374 |
rs31317076 | snp | A/T | 0.497041 | 0.0383476 | intron-variant | Rfwd2 | Mm_Celera | 1:159343563 | AGAATGTGATCCTTC[A/T]CTATATTCTTACAGA | 26374 |
rs31317077 | snp | C/T | 0.5 | 0 | intron-variant | Rfwd2 | Mm_Celera | 1:159343497 | TTGTTATAAATAAAA[C/T]TTTGGATAGAGAGTT | 26374 |
rs31317078 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159343305 | TAGAGAGAAAAGTTT[A/G]GTGTCCCGTAATCTG | 26374 |
rs31317079 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159343267 | TAGGGTTTTGTTCCT[C/T]CTTGCTAAGGTGGGA | 26374 |
rs31317080 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159343085 | CAGATAGAAACAGAG[A/G]AAGGCTATTGAGCAC | 26374 |
rs31317081 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Rfwd2 | Mm_Celera | 1:159343059 | GTAAGCAAGATGGAT[G/T]ACTAGATGGTCAGAT | 26374 |
rs31317082 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159343039 | CAATCATGCTTATTG[A/G]GGTTGTAAGCAAGAT | 26374 |
rs31317083 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159342993 | GACTTAACTGAAGTT[A/G]AAAGAAATAGGTAGC | 26374 |
rs31317084 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159297065 | TAAAAGAAAGCAAGT[A/G]TGATTGATAATTATA | 26374 |
rs31317085 | snp | A/T | 0.359862 | 0.224567 | intron-variant | Rfwd2 | Mm_Celera | 1:159297006 | AAAGATTTTATTTTT[A/T]AAAACATGTAGTTGA | 26374 |
rs31317086 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Rfwd2 | Mm_Celera | 1:159296764 | CAAGTTTGTTCTGTG[C/T]GCAAATCATTGTTTA | 26374 |
rs31317087 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Rfwd2 | Mm_Celera | 1:159296563 | AAATAAAATAAACCC[A/G]AATTTCTTAAATATT | 26374 |
rs31317088 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159296356 | TATAGAACTGGTGGG[C/T]AAAATGAATCCTGCC | 26374 |
rs31317089 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159296193 | TGCTTCAAGAATAAA[C/G]CAAAATGAGCTGTTT | 26374 |
rs31317090 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Rfwd2 | Mm_Celera | 1:159296131 | AAAATTGTAAAAATA[C/T]AGTTCCTCCATAAAA | 26374 |
rs31317091 | snp | A/G | 0.42 | 0.183303 | intron-variant | Rfwd2 | Mm_Celera | 1:159295656 | AAAAATATTTTCCTC[A/G]TGTTTATAATTCTTT | 26374 |
rs31317092 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159295594 | ACAGCAATTTAGTGA[A/C]TTTATTTATATACAT | 26374 |
rs31317093 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159295550 | GAAATAAATGAATAC[A/G]TACCACTTACCCTAC | 26374 |
rs31317124 | snp | A/C/T | 0.48 | 0.0979796 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159270199 | CCATGTGGAAGAGAG[A/C/T]GAAGTCATTCTTGAC | 26374 |
rs31317125 | snp | G/T | 0.32 | 0.24 | intron-variant | Rfwd2 | Mm_Celera | 1:159270079 | AATATTCTGTTTTAG[G/T]TAGTTGAGCTTTTCC | 26374 |
rs31317126 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Rfwd2 | Mm_Celera | 1:159269884 | TTAGATTTTATGAAT[C/G]TTGAAGATTATATTT | 26374 |
rs31317127 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159269787 | ATCCCAAACATTTCA[A/G]TAGTAAACTGGTAAT | 26374 |
rs31317128 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159269621 | GGCCAGATGTGTTAT[C/T]TGTAAGCCTGTCATT | 26374 |
rs31317129 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159269599 | CTGTTTTAATAAACA[C/T]CCTAAAGGCCAGATG | 26374 |
rs31317130 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Rfwd2 | Mm_Celera | 1:159269571 | ATATGCTAGTAATTC[A/C]CCTGTTTCATAACTG | 26374 |
rs31317131 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159269118 | CTCGTTTCAGACTCC[C/T]AGTCCTTTCATCTCA | 26374 |
rs31317132 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159269101 | TTCTTAAGTTGCCCA[G/T]ACTCGTTTCAGACTC | 26374 |
rs31317133 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Rfwd2 | Mm_Celera | 1:159269058 | ATGGTGTGGGTGAGT[A/G]TGCTGGTTTGTAGAG | 26374 |
rs31317354 | snp | A/T | 0.459184 | 0.136902 | intron-variant | Rfwd2 | Mm_Celera | 1:159247321 | ACTTCATTAACTTTT[A/T]TTTTCATTTTAACCT | 26374 |
rs31317355 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159247142 | TAGGTTGTTATTAGT[A/G]GAAACTTCTGCTTTA | 26374 |
rs31317356 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Rfwd2 | Mm_Celera | 1:159246307 | ATTTTCCCCACTTTC[C/T]ACTCCTAACCTATTT | 26374 |
rs31317357 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Rfwd2 | Mm_Celera | 1:159246184 | TCAGATGTGGAAGGC[A/T]AAAAGGAAATTCTGA | 26374 |
rs31317358 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rfwd2 | Mm_Celera | 1:159246138 | TTTTTGTGTATAACC[A/G]TTCATAGTATCATTC | 26374 |
rs31317359 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Rfwd2 | Mm_Celera | 1:159245370 | AGGCAGACCCTGTCT[C/T]AAATTAGTAGTTTTA | 26374 |
rs31317360 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159245124 | ATCCCTGGATGAGGC[A/G]GATGTAGAGTATATG | 26374 |
rs31317361 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159244712 | GAAATTATTTTTACT[A/G]TACTCTTTACACAAA | 26374 |
rs31317362 | snp | C/T | 0.391111 | 0.206368 | synonymous-codon, intron-variant | Rfwd2 | GRCm38.p3 | 1:159244631 | GGACAATAATAGATG[C/T]CCCAAGTGTAATTAT | 26374 |
rs31317363 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159243715 | AAATGCAGTACACCA[A/C]AAAAATATAAGAAAC | 26374 |
rs31317774 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159342980 | TTCCCTCAAAAATGA[C/T]TTAACTGAAGTTGAA | 26374 |
rs31317775 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159342775 | CCCTCCAGGAAACCC[G/T]CCTCTGTTCTAAAGC | 26374 |
rs31317776 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159342602 | TGTGCTCTTTATATG[C/T]AGATGAGTCCCGGTT | 26374 |
rs31317777 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159342409 | AATGTACTGCTCTTT[A/C]CATTTAAATCTTTTT | 26374 |
rs31317778 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Rfwd2 | Mm_Celera | 1:159341928 | TAGGCTGGTCATAAA[C/T]TCCATGGTTTTATTT | 26374 |
rs31317779 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Rfwd2 | Mm_Celera | 1:159341917 | AGCATTTTTCATAGG[A/C]TGGTCATAAACTCCA | 26374 |
rs31317780 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Rfwd2 | Mm_Celera | 1:159341547 | GTATTTATAGTTTTA[C/T]GATAGTGTTGTTTTT | 26374 |
rs31317781 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rfwd2 | Mm_Celera | 1:159341411 | CTTCATGAGCTGCTG[A/G]TTCTTGGCCTTGGTT | 26374 |
rs31317782 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159341351 | CCTAGGCACATGGCA[A/G]GATTACTAGTTTAAT | 26374 |
rs31317783 | snp | C/G | 0.5 | 0 | intron-variant | Rfwd2 | Mm_Celera | 1:159341158 | GAGGCACACAGCACT[C/G]GGGTATACTGTGAGC | 26374 |
rs31317874 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159323964 | TGCTATTCAAGAGAA[C/T]AGTAGGAGTACTTAG | 26374 |
rs31317875 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159323718 | AAACTCTCTTTGACA[A/G]CTTATATTCATTTTG | 26374 |
rs31317876 | snp | C/T | 0.42 | 0.183303 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159321841 | AACTGTGAATGCCAC[C/T]AGGCTCCTATTCCTG | 26374 |
rs31317877 | snp | A/G | 0.32 | 0.24 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159321776 | CTTTCTTGAGTAACC[A/G]TGGCTTAAAAGAAAG | 26374 |
rs31317878 | snp | A/G | 0.32 | 0.24 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159321696 | CAGAATCAGTTCAGT[A/G]GGTCTACATTTATTC | 26374 |
rs31317879 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159321315 | AGTAGAAGTAGTGTA[A/G]TAATCTTTTTTTCTG | 26374 |
rs31317880 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Rfwd2 | Mm_Celera | 1:159321069 | TAGTTTCGTTCTATA[C/T]TGTGCTACTTTTTTC | 26374 |
rs31317881 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rfwd2 | Mm_Celera | 1:159320741 | AATATTTTTCCCTGG[C/T]ATAAATTCTGATTGT | 26374 |
rs31317882 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Rfwd2 | Mm_Celera | 1:159320339 | CATTTATCATGTAGC[A/G]TGGTGGTTTTCATTG | 26374 |
rs31317883 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Rfwd2 | Mm_Celera | 1:159320169 | AGCCTGTTCATTTCT[C/T]TGACTATTCATTTTC | 26374 |
rs31318004 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159295524 | CGATTTAATCGGAAC[A/G]TAACACTCCTGAAAT | 26374 |
rs31318005 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rfwd2 | Mm_Celera | 1:159295509 | CTACAGATCATAATA[C/T]GATTTAATCGGAACG | 26374 |
rs31318006 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159294937 | ATAGTCTGTTAGGAT[A/G]TGGTTTTGGTCCAGC | 26374 |
rs31318007 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Rfwd2 | Mm_Celera | 1:159291434 | ATATTGTAATGTATT[A/G]TTTATTGAAGAATGC | 26374 |
rs31318008 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rfwd2 | Mm_Celera | 1:159291228 | ACAAAGTAGTGCATT[C/T]TTTAGGTCCTTTATG | 26374 |
rs31318009 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Rfwd2 | Mm_Celera | 1:159291052 | GGAGAGGAAGTTGAA[A/G]TAAGGGGAAGTATGA | 26374 |
rs31318010 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159290875 | GTGTATAGTAGTGCT[A/G]CTTCATGAATTTCTG | 26374 |
rs31318011 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Rfwd2 | Mm_Celera | 1:159290302 | ATAATATCTGTGCCA[A/G]TTACCTTATTGCACT | 26374 |
rs31318012 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Rfwd2 | Mm_Celera | 1:159290224 | TTCTAATGAAATGGG[C/G]TTAAAAAACACTAAA | 26374 |
rs31318013 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Rfwd2 | Mm_Celera | 1:159289936 | CATTCAAAGAGATGA[G/T]TTACATTTAAATATT | 26374 |
rs31318124 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159268972 | CTGCTACAGCTCAAC[C/T]TGCTTCCCAAGTGCT | 26374 |
rs31318125 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Rfwd2 | Mm_Celera | 1:159268894 | GTCTTCCTACTTTGT[G/T]TTTTTCAATCTGTCT | 26374 |
rs31318126 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Rfwd2 | Mm_Celera | 1:159268887 | TGTTCAAGTCTTCCT[A/G]CTTTGTGTTTTTCAA | 26374 |
rs31318127 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159268073 | TGCATCTGTTGTTTG[A/G]AGTATGTACAATAAC | 26374 |
rs31318128 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159268027 | AGCTGTGGCTAGAAC[A/T]GAATGTAATGCCACA | 26374 |
rs31318129 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Rfwd2 | Mm_Celera | 1:159267986 | TTGTATTCTATGGAA[A/G]GGAATCCTTGAGAGG | 26374 |
rs31318130 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159267702 | GTAGATTACTCCTAG[A/C]GAGTGACAGACATAT | 26374 |
rs31318131 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Rfwd2 | Mm_Celera | 1:159267533 | AGAACATTCCACATA[A/G]AAAGGCCAGTCATGA | 26374 |
rs31318132 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159267427 | ATATTTACATTACCC[A/G]TTAAGCCATTTTGAG | 26374 |
rs31318133 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Rfwd2 | Mm_Celera | 1:159267215 | CATAATAAAGTTCAG[A/G]TTACTTACAGAAATT | 26374 |
rs31318264 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159243691 | TACTGATGAAGGAAG[A/C]AATTGTTAAAATGCA | 26374 |
rs31318265 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Rfwd2 | Mm_Celera | 1:159243530 | ACAGTTATAAAAGGT[C/T]TATTATTGAAAAGAA | 26374 |
rs31318266 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Rfwd2 | Mm_Celera | 1:159243115 | GTGAGGGAGTAGACA[A/G]GTAGAGCAGTGACCC | 26374 |
rs31318267 | snp | C/G | 0.486111 | 0.0821678 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159243113 | AAGTGAGGGAGTAGA[C/G]AAGTAGAGCAGTGAC | 26374 |
rs31318268 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159243025 | TTTAGTAGATACTGG[A/C]GTCTGGGGTTCATTA | 26374 |
rs31318269 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Rfwd2 | Mm_Celera | 1:159242855 | CCTTTAGTAAAAATG[A/G]AAATGAAAATGCTTA | 26374 |
rs31318270 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rfwd2 | Mm_Celera | 1:159241520 | TTAAAATAAAGTTAT[A/G]GCATTTTGTATTCTT | 26374 |
rs31318271 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Rfwd2 | Mm_Celera | 1:159241464 | GTTAGTTAGGTTTGG[A/G]CTAAACCAACATACT | 26374 |
rs31318272 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159241451 | AATATGATTCAGGGT[A/T]AGTTAGGTTTGGACT | 26374 |
rs31318273 | snp | C/T | 0.32 | 0.24 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159241326 | TTAATCTTAGTATTT[C/T]TTTTGTCCATATTGG | 26374 |
rs31318664 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159341095 | TGAAGTGTTTGAGTC[A/G]AAGTTTGGGTGGGAG | 26374 |
rs31318665 | snp | A/G | 0.391111 | 0.206368 | intron-variant, downstream-variant-500B | Rfwd2, Scarna3a, Mir1843b | GRCm38.p3 | 1:159340834 | ATTTTGTATACGAAG[A/G]GACTATTGAAAGTGT | 26374 |
rs31318666 | snp | A/G | 0.459184 | 0.136902 | intron-variant, downstream-variant-500B | Rfwd2, Scarna3a, Mir1843b | Mm_Celera | 1:159340697 | TGGTAGTTTTTGAAA[A/G]TAGTTATTACTATTG | 26374 |
rs31318667 | snp | C/T | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Rfwd2, Scarna3a, Mir1843b | Mm_Celera | 1:159340653 | CCTAGATTGGAATTC[C/T]TGCCTCTACTATTTA | 26374 |
rs31318668 | snp | A/T | 0.391111 | 0.206368 | intron-variant, downstream-variant-500B | Rfwd2, Scarna3a, Mir1843b | Mm_Celera | 1:159340624 | TTAAAATAAAGACTC[A/T]CATCACCTACATTCC | 26374 |
rs31318669 | snp | A/G | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Rfwd2, Scarna3a, Mir1843b | GRCm38.p3 | 1:159339659 | TCAGCTTTGTTGTAT[A/G]TCTTTATCTTCCATT | 26374 |
rs31318670 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Rfwd2, Scarna3a, Mir1843b | GRCm38.p3 | 1:159339633 | TGTCATTTAAGGCAA[A/G]TGCCATAGAATCAGC | 26374 |
rs31318671 | snp | G/T | 0.493827 | 0.0552116 | intron-variant, upstream-variant-2KB | Rfwd2, Scarna3a, Mir1843b | Mm_Celera | 1:159339484 | TAAGACAGTTGAGCA[G/T]TGAGAATTTAAATCA | 26374 |
rs31318672 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Rfwd2, Scarna3a, Mir1843b | GRCm38.p3 | 1:159339328 | TAACACATGGGCCAC[A/G]TTCCAAACTAGTGAA | 26374 |
rs31318673 | snp | C/G | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Rfwd2, Scarna3a, Mir1843b | GRCm38.p3 | 1:159339260 | CCCAATCCCCAAGAT[C/G]TGCTTGCCAAATATT | 26374 |
rs31318844 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Rfwd2 | Mm_Celera | 1:159320044 | AACACATAGAGACAG[A/G]CTTGTGGAGTTTTGT | 26374 |
rs31318845 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159319911 | AGTGCATTTGAAAAC[A/G]AATTGGTTACTTTTA | 26374 |
rs31318846 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159319006 | GTTATTTATTCTGTT[A/C]GTCTTATCTGTGCCA | 26374 |
rs31318847 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Rfwd2 | Mm_Celera | 1:159318411 | AAACCCAGTTCCTCT[A/G]CAAGAACAGCAGGTG | 26374 |
rs31318848 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159318000 | ACTTGGCTTCTTATG[C/T]CTAGCTTTTTTCATT | 26374 |
rs31318849 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159317959 | CCAGCTTCCATGAGG[A/G]TAACTTTTTAGTTTT | 26374 |
rs31318850 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159317591 | TTAAGTGATTCATAA[A/G]GGCATACAAATTGCG | 26374 |
rs31318851 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159317568 | TAATCTGCAAGTGTG[G/T]TGGTACTTTAAGTGA | 26374 |
rs31318852 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159317465 | AAGAGATTTTCGAGA[C/T]GGCTAGTGGGGTTGT | 26374 |
rs31318853 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159317151 | TTTCATCAGCCCTAA[C/G]TGATCTTTACAATAT | 26374 |
rs31319014 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Rfwd2 | Mm_Celera | 1:159289332 | TCTTTCTGAATATTA[A/G]TGTTTGATTCTCCAG | 26374 |
rs31319015 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159289202 | GAATGCTCAGTAGCA[G/T]CCATCTGACAGGAGG | 26374 |
rs31319016 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159289192 | TAGCAAATTAGAATG[C/T]TCAGTAGCATCCATC | 26374 |
rs31319017 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Rfwd2 | Mm_Celera | 1:159288793 | AGCATACTGCTTTTT[A/T]AAAAAATCTTCAAAA | 26374 |
rs31319018 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159288769 | CTAAAAGATCACCTA[A/G]TTAATTTGAGCATAC | 26374 |
rs31319019 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rfwd2 | Mm_Celera | 1:159288369 | GGACCTTGTGTGATG[C/T]CATTACTGTTGTCTT | 26374 |
rs31319020 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rfwd2 | Mm_Celera | 1:159288223 | AACTGCCTTGAAAAA[C/T]TGAGTATTGTAATTG | 26374 |
rs31319021 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159288205 | TTTAAAATGCAGATT[G/T]CCAACTGCCTTGAAA | 26374 |
rs31319022 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159287975 | TTAATTTTGTCTATC[A/G]TTTCTTCAGATAATA | 26374 |
rs31319023 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Rfwd2 | Mm_Celera | 1:159287483 | GGTTGCTAGATGAAT[G/T]TTGACTGCCTAAATC | 26374 |
rs31319264 | snp | C/G | 0.33241 | 0.236027 | intron-variant | Rfwd2 | Mm_Celera | 1:159266555 | TAAAAAGTATGATCT[C/G]TATTTGAATGTCAGC | 26374 |
rs31319265 | snp | G/T | 0.387812 | 0.208586 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159266440 | GATGTGAAAGCTTTT[G/T]GGGTATCTTATATTT | 26374 |
rs31319266 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159266320 | TTAAAAATCATAATA[C/T]GTAACTATGATAGTG | 26374 |
rs31319267 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159266221 | TCAATATTTATCCTA[C/T]TACTGAAATGCTTAC | 26374 |
rs31319268 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Rfwd2 | Mm_Celera | 1:159265546 | AATCTATAAATGGTA[G/T]TTTCAAATGTTATTT | 26374 |
rs31319269 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159264506 | AAAGTGGTCAGTGGA[A/G]CAGCTTATATTTGAA | 26374 |
rs31319270 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159264494 | TGGGGCATTAAAAAA[G/T]TGGTCAGTGGAACAG | 26374 |
rs31319271 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159264493 | CTGGGGCATTAAAAA[A/G]GTGGTCAGTGGAACA | 26374 |
rs31319272 | snp | C/T | 0.5 | 0 | intron-variant | Rfwd2 | Mm_Celera | 1:159264385 | AACTGCATAATCTTA[C/T]GTGTACTTTGTATGT | 26374 |
rs31319273 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Rfwd2 | Mm_Celera | 1:159264283 | AAAGTCTAAACCACT[G/T]GGATTTTAAATGTCT | 26374 |
rs31319284 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Rfwd2 | Mm_Celera | 1:159241300 | TCCATATATTTTATT[A/G]GCATATCAGATTAAT | 26374 |
rs31319285 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159239933 | AAGAATGAAAAAGGC[C/T]TGCACTGTCTTTGTT | 26374 |
rs31319286 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159239470 | ATATATTAAATTTGG[C/T]TTGATTGATTTTTGT | 26374 |
rs31319287 | snp | A/T | 0.387812 | 0.208586 | intron-variant | Rfwd2 | Mm_Celera | 1:159239328 | GAATAATGTAAGTGT[A/T]CTCATTTCACATATT | 26374 |
rs31319288 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159239286 | ATAAGGTTCCACCCT[A/G]AATTCTATGGGATGG | 26374 |
rs31319289 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Rfwd2 | Mm_Celera | 1:159239217 | CTCAGGGTAGCCGGG[A/C]TAGTGTTTCTGAGCA | 26374 |
rs31319290 | snp | A/C | 0.35503 | 0.226867 | intron-variant | Rfwd2 | Mm_Celera | 1:159238955 | AGAAAGGATTGAACA[A/C]CTTACTATATAACAT | 26374 |
rs31319291 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Rfwd2 | Mm_Celera | 1:159237954 | ATAAAATATACTTGC[C/T]TCCAGACATGAATAT | 26374 |
rs31319292 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159237604 | GTTAGTGCTTGTGCT[A/G]TGAATGCCTACAAAA | 26374 |
rs31319293 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Rfwd2 | Mm_Celera | 1:159237533 | TAACAAAGGTGGAAA[C/T]TGATGCGGCTGTTCT | 26374 |
rs31319504 | snp | A/G | 0.401235 | 0.199068 | intron-variant, upstream-variant-2KB | Rfwd2, Scarna3a, Mir1843b | GRCm38.p3 | 1:159339228 | GAGAAAATATCCCCA[A/G]TGACCTAACAGTGCA | 26374 |
rs31319505 | snp | A/G | 0.426035 | 0.177515 | intron-variant, upstream-variant-2KB | Rfwd2, Scarna3a, Mir1843b | Mm_Celera | 1:159338969 | TAATAATCTGTGGCT[A/G]CTTTGAATTTTGTTA | 26374 |
rs31319506 | snp | C/T | 0.497041 | 0.0383476 | intron-variant, upstream-variant-2KB | Rfwd2, Scarna3a, Mir1843b | GRCm38.p3 | 1:159338968 | TTAATAATCTGTGGC[C/T]ACTTTGAATTTTGTT | 26374 |
rs31319507 | snp | A/G | 0.290657 | 0.246672 | intron-variant, upstream-variant-2KB | Rfwd2, Scarna3a, Mir1843b | Mm_Celera | 1:159338799 | AAACTGGTCACTGCT[A/G]TCTTGTAAACCTGCA | 26374 |
rs31319508 | snp | C/T | 0.345679 | 0.230967 | intron-variant, upstream-variant-2KB | Rfwd2, Scarna3a, Mir1843b | Mm_Celera | 1:159338709 | AGTTTATTGACTACA[C/T]ACTGACACAGATGAG | 26374 |
rs31319509 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Rfwd2, Scarna3a, Mir1843b | Mm_Celera | 1:159338601 | GAGGGTAAAGTAAAA[A/G]CACGTTTATCCAGGT | 26374 |
rs31319510 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Rfwd2, Scarna3a, Mir1843b | Mm_Celera | 1:159338522 | ACTTTTCACAGTGAC[C/T]CTCCAAGGGGCATTT | 26374 |
rs31319511 | snp | A/G | 0.415225 | 0.187619 | intron-variant, upstream-variant-2KB | Rfwd2, Scarna3a, Mir1843b | GRCm38.p3 | 1:159338490 | ACCATGCCCAGTAGA[A/G]CTACCTGAGGGACCA | 26374 |
rs31319512 | snp | A/G | 0.35503 | 0.226867 | intron-variant, upstream-variant-2KB | Rfwd2, Scarna3a, Mir1843b | Mm_Celera | 1:159338406 | AAAGTTTCTGAAGAT[A/G]AGACCTCTGGTCCAT | 26374 |
rs31319513 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159338087 | CCATTGGTTGAGGCT[C/G]TCATCATTCCCTTGA | 26374 |
rs31319884 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159287463 | ATTTGGATCCCTTTA[A/T]TCCAGGTTGCTAGAT | 26374 |
rs31319885 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Rfwd2 | Mm_Celera | 1:159287295 | TCATATCCACAACAC[A/T]GCAGTAGTTAGTTTT | 26374 |
rs31319886 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159287133 | CATCTCCAGCTAGGA[G/T]TGCATTTACACTAGA | 26374 |
rs31319887 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159286893 | ATAGCAATGACAATT[A/G]GTATACATTTAGATG | 26374 |
rs31319888 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159286833 | ATATAGATGTTGATC[A/T]TAACACAGCTGAACC | 26374 |
rs31319889 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159286737 | AGTAATGAAAAGTCA[C/T]TAAGAAAAAGAAAAG | 26374 |
rs31319890 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159286652 | CTCTGCCTGGCCTTG[C/T]AGTTTTAAAAATGAC | 26374 |
rs31319891 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Rfwd2 | Mm_Celera | 1:159286478 | ATTAATGTCTATATC[A/G]TGCTTAAAGCATGTT | 26374 |
rs31319892 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Rfwd2 | Mm_Celera | 1:159286171 | CTACAATAAGGAGTG[A/G]TTAAGTAAATAGTAG | 26374 |
rs31319893 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159285572 | TCAAACAAATATTTA[A/G]TAGTTATAGGCAAGG | 26374 |
rs31320014 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159237421 | TCCTTCTATGAACCC[A/T]TTAAGCATCTCTGTT | 26374 |
rs31320015 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159236893 | TGTAATCAACCTATC[C/T]TCTTTATTGACTGTT | 26374 |
rs31320016 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Rfwd2 | Mm_Celera | 1:159236854 | TTGCTGGCAATTTTA[C/T]CAATACTTGATAAGA | 26374 |
rs31320017 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rfwd2 | Mm_Celera | 1:159236299 | GACATCTCAATCAAG[A/G]ATGTTAAAAACAATA | 26374 |
rs31320018 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159236206 | CCAGAAGATAGGATG[C/T]CTTTCTTGTTGAACA | 26374 |
rs31320019 | snp | G/T | 0.387812 | 0.208586 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159235955 | GTAGATAAGGACATT[G/T]CCTTTTCTCCAACTC | 26374 |
rs31320020 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159235679 | TTTTATTTACTATAG[C/T]ACCAGTGTAATGATT | 26374 |
rs31320021 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159235302 | TCTGAATCTTTTACC[A/G]TGTAAGAATCTCAGT | 26374 |
rs31320022 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159234978 | TTAGTTCATCACCTT[A/G]TTGTTTAAAAGAAAT | 26374 |
rs31320104 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Rfwd2 | Mm_Celera | 1:159315237 | AAGTGAAATCCTTAT[A/G]CACTTTTACAAAGGT | 26374 |
rs31320105 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159315060 | TCTGCACCTTGGCTC[A/G]TTGTGGGTCTTTGTG | 26374 |
rs31320106 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rfwd2 | Mm_Celera | 1:159313854 | AATGTTTTTGACCCT[C/T]ATCTGTGATCCCCTT | 26374 |
rs31320134 | snp | C/T | 0.42 | 0.183303 | intron-variant | Rfwd2 | Mm_Celera | 1:159263975 | TAAATTATTTGATAT[C/T]AGCCATTTTTTTGTA | 26374 |
rs31320135 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159263653 | GATAACTTTTGACAT[A/C]TTTTTTATATTCATG | 26374 |
rs31320136 | snp | G/T | 0.46875 | 0.121031 | intron-variant | Rfwd2 | Mm_Celera | 1:159263509 | TTCAAATATTTGTTT[G/T]TTGTCTTCTGTGTAC | 26374 |
rs31320137 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rfwd2 | Mm_Celera | 1:159263466 | TTGGAGGTTATAATG[C/T]CTATAGGCTTAAGTT | 26374 |
rs31320138 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Rfwd2 | Mm_Celera | 1:159263396 | AGTCCACCTTCAAGG[A/G]CTTACTTATTTCTCA | 26374 |
rs31320139 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Rfwd2 | Mm_Celera | 1:159263384 | TTACATGATAGCAGT[C/T]CACCTTCAAGGGCTT | 26374 |
rs31320140 | snp | A/C | 0.42 | 0.183303 | intron-variant | Rfwd2 | Mm_Celera | 1:159263307 | TTTTAGTGGCTTCAA[A/C]TTACACAATTGTATT | 26374 |
rs31320141 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159263235 | TTACACTGTTCATAG[A/C]GTGTCTTAGGAATGT | 26374 |
rs31320142 | snp | A/T | 0.5 | 0 | intron-variant | Rfwd2 | Mm_Celera | 1:159262950 | GTTTCTCCTTTAGAA[A/T]TAGTAAACCTTGAGC | 26374 |
rs31320143 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159262113 | CATTGTCCTTAATAT[C/G]TTTTCTCCATGATTT | 26374 |
rs31320884 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159285341 | TTGCTCATCTTTGAA[G/T]GTTGGATACTAGTAG | 26374 |
rs31320885 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Rfwd2 | Mm_Celera | 1:159284918 | TATATAAGCTCCATT[C/T]AGTTAGCGCCTATTC | 26374 |
rs31320886 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159284861 | CCAGAATGTTTTATC[A/G]TTCCAGAGCAAGCTA | 26374 |
rs31320934 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159261948 | AAAACAACATTCCTA[C/T]TACAGTTGCCTATTG | 26374 |
rs31320935 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Rfwd2 | Mm_Celera | 1:159261818 | TACACTTTGTCTCTC[A/T]TGTGTTTAGACCTAA | 26374 |
rs31320936 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159261536 | ACTTCTTTGAGTCTT[C/T]GTGGTCCTGCTATAT | 26374 |
rs31320937 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Rfwd2 | Mm_Celera | 1:159260105 | TGCTAGTTTGATGCA[C/T]CATAATGAAACACTG | 26374 |
rs31320938 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159259971 | CTTGGTTCTTTTTGT[C/T]TTAGCTACATCAAAT | 26374 |
rs31320939 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159259489 | ACTCTTCTGGTTTTC[C/T]TTTGTTTGTGGGTCA | 26374 |
rs31320940 | snp | A/C | 0.426035 | 0.177515 | intron-variant | Rfwd2 | Mm_Celera | 1:159259130 | GCAATTGTGTGTACT[A/C]ATGTGTGGTTTTGAT | 26374 |
rs31320941 | snp | G/T | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Rfwd2 | Mm_Celera | 1:159257623 | ATTACATAATAAGAC[G/T]TTGTAGCTTTTCCAT | 26374 |
rs31320942 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Rfwd2 | Mm_Celera | 1:159257555 | AGATTGAGCACTTTG[A/G]TATTATAGTCACTGG | 26374 |
rs31325738 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159253731 | ATACTATATTCTAGA[C/G]TGTTAACTTAAAAAA | 26374 |
rs31335548 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Rfwd2 | GRCm38.p3 | 1:159231660 | TGGCTCTTTCAGATT[A/G]AAACCTAAGGCTTGT | 26374 |
rs31346153 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159303618 | TCTCCACATCCTCGT[C/T]AGCATCTGCTGTCAC | 26374 |
rs31374407 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159295309 | TGATAGATTTTTATT[A/G]TTCTGAAATGAGTTA | 26374 |
rs31382666 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159334441 | TAGAACAATGAGTAA[C/T]GAGCCACTGGGGATT | 26374 |
rs31422689 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159265165 | ATACCTGGCATGAGA[A/G]GATTAAATCACAGGG | 26374 |
rs31434011 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159295194 | TAGGTAGCCTAAAAT[A/G]AAGAACAGTTTCTAC | 26374 |
rs31461704 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159276545 | CCCAACCCCTTTTTC[C/T]ACAAGAATGTCCCCA | 26374 |
rs31478858 | snp | C/G | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159318525 | TATTGACAGCTAGTT[C/G]TCTGAAATAGGAAGC | 26374 |
rs31486916 | snp | A/T | 0.32 | 0.24 | intron-variant | Rfwd2 | Mm_Celera | 1:159262499 | GTCATATATTTGGGT[A/T]GGGTCTCTGACATGA | 26374 |
rs31525774 | snp | G/T | 0.5 | 0 | intron-variant | Rfwd2 | Mm_Celera | 1:159250926 | TTTTAAAAATGATAC[G/T]ATTTTCTACATATAT | 26374 |
rs31549483 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159264920 | TTTGTCTTTATTTTA[A/C]CTATTGTAAAATTGT | 26374 |
rs31560782 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159332757 | ACTGATACTTTCCCA[C/T]TGTGAATTTTATCTT | 26374 |
rs31567833 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159318401 | CTCTTGAATCAAACC[A/C]AGTTCCTCTACAAGA | 26374 |
rs31621142 | snp | A/C | 0.32 | 0.24 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159240280 | TATTTCACATAATGC[A/C]CTTTGCATTCTTCTG | 26374 |
rs31646397 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159310835 | TACATGTGTCTTTGT[A/G]GAAGTATTATGTCCA | 26374 |
rs31652624 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159291013 | ATATTTAGTTTAAGA[C/T]ACTGTGGTCAATCCT | 26374 |
rs31715172 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159318405 | TGAATCAAACCCAGT[G/T]CCTCTACAAGAACAG | 26374 |
rs31744848 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159255904 | GCATACACAGGTCAG[A/G]GGGCACCTTGAGAAG | 26374 |
rs31750615 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159304647 | GTGATTGGGTTACCT[A/C]ACTCAGGATGATATC | 26374 |
rs31769504 | snp | C/T | 0.32 | 0.24 | intron-variant | Rfwd2 | Mm_Celera | 1:159240406 | GTTAAGTTGATTCAG[C/T]CTCCTGGCTCCAAAG | 26374 |
rs31771179 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159323351 | AATCTTTCCTTAGGC[A/C]TATTAATATTTTTCA | 26374 |
rs31771946 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159272481 | ATAATATGTATTATT[A/G]TATTCAACTATATGA | 26374 |
rs31820931 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159241249 | GCTTATCACTGGAAG[A/G]GCATTCTACTTGGAA | 26374 |
rs31822522 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159335696 | GGAAATCACCAGAGT[A/G]CTGCTGACTCTTTCC | 26374 |
rs31823858 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159239442 | AGAAGGGTAGAATTC[A/T]TAATTCTTAGCTATA | 26374 |
rs31842149 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159285466 | ACACTCACATCAGAA[G/T]ACTGTGTATAACCAG | 26374 |
rs31854927 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159271356 | CCCTCTTCTGGTGTG[C/T]CTGAAGATAGCAACA | 26374 |
rs31873643 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159259394 | TGTTTGTGGGGGAGC[A/G]TGCAGTTGTGTTTTT | 26374 |
rs31881891 | snp | A/T | 0.32 | 0.24 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159240135 | ACTATACCTGTAAAA[A/T]CAATGCTTTACTTTC | 26374 |
rs31897328 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159240076 | GTTGTGCTATGTTTA[C/T]TTGTTGGACAGTGTC | 26374 |
rs31909037 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159233462 | TTCACACCCAATTCC[A/T]GGTTTCAACTGTTGG | 26374 |
rs31909589 | snp | A/T | 0.5 | 0 | intron-variant | Rfwd2 | Mm_Celera | 1:159266654 | TTCTTGTTTTTCTTT[A/T]TTTTCTTTAAACCAA | 26374 |
rs31920204 | snp | C/T | 0.32 | 0.24 | intron-variant | Rfwd2 | Mm_Celera | 1:159322261 | TATGTTTCTTTCCTG[C/T]CTTCTTCAGTTTTTT | 26374 |
rs31929697 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159232989 | CAGAGTTAAGGTTCC[C/T]GGTTGGGAGGTGGAG | 26374 |
rs31941951 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159291444 | GTATTATTTATTGAA[A/G]AATGCTTATGAGTTT | 26374 |
rs31952146 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159289580 | AGTCTGATACCCAGA[A/G]CCCATGTGAAATAAA | 26374 |
rs31956778 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159292288 | TCTTAGGTCCAGGAA[C/T]GGTGGTACATGCCTT | 26374 |
rs31961244 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159318406 | GAATCAAACCCAGTT[A/C]CTCTACAAGAACAGC | 26374 |
rs31965640 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159314595 | TTTATTAGTTCTTTT[A/G]AGAATTTCATGGCTT | 26374 |
rs31969479 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159290744 | ACTTTTGGAAGAGCA[C/G]TCGGTGCTCTTAACC | 26374 |
rs31979722 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159303908 | TAATTTCAATTAAAA[A/T]TTTTTTTTTAATTTT | 26374 |
rs32015636 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159335645 | AATCATCAGCTCTCC[A/T]TTATTTTACAAATTA | 26374 |
rs32018672 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159336969 | GAGTCTTCTTTGTAG[G/T]CTAGGATAATGGAGG | 26374 |
rs32046107 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159307269 | GCTAATATGTAGAGC[A/G]GTGCAGAGTGAGGGA | 26374 |
rs32060160 | snp | G/T | 0.5 | 0 | intron-variant | Rfwd2 | Mm_Celera | 1:159255480 | GCAGGTCTTTTCTCG[G/T]GTAGCCGATATTTTG | 26374 |
rs32102044 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159251714 | CTTTTTCTTGTTTTT[G/T]TTGTTGTTGTTGTTT | 26374 |
rs32135698 | snp | A/C | 0.5 | 0 | intron-variant | Rfwd2 | Mm_Celera | 1:159316798 | TGAGGGTGCTCCCCC[A/C]CCCACCCATTCCCTT | 26374 |
rs32149605 | snp | C/G | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159336067 | GCTGCTTATGCCATC[C/G]AAGAAAGAAAGGAAA | 26374 |
rs32154867 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159290221 | TTCTTCTAATGAAAT[A/G]GGCTTAAAAAACACT | 26374 |
rs32178009 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159259121 | AAACATCAAGCAATT[A/G]TGTGTACTAATGTGT | 26374 |
rs32181862 | snp | G/T | 0.32 | 0.24 | intron-variant | Rfwd2 | Mm_Celera | 1:159260213 | ACATAGCTCAGGCTG[G/T]CCTTGAATTCTCAAT | 26374 |
rs32184048 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159243642 | GTCATCCTTTGACCC[C/G]TGGCATATGCCTCCT | 26374 |
rs32195847 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159233451 | GTCAAAGTTTGTTCA[C/T]ACCCAATTCCAGGTT | 26374 |
rs32209744 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159286126 | GTTTAAATCCTTTAT[C/T]AAATGTCTATAATAG | 26374 |
rs32215817 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159250008 | GTTTGTTTTTGTTTG[C/T]TTGTTTAATTTTAGA | 26374 |
rs32266911 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159269590 | GTTTCATAACTGTTT[C/T]AATAAACATCCTAAA | 26374 |
rs32285515 | snp | C/T | 0.5 | 0 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159251003 | TCTTTACCTCTTTTC[C/T]CCTCCCACCAAGCCC | 26374 |
rs32303399 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159238556 | TCTCCTGCCTCCCCC[G/T]CCAAAAAAGAAAGAA | 26374 |
rs32306691 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159305189 | GAACTCAAATACTGC[A/C]GGAAGCTGGAAGCCA | 26374 |
rs32330512 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159290972 | ATGCAGCTCCTCATG[C/T]TGTGGATTATTATTT | 26374 |
rs32332417 | snp | A/G | 0.5 | 0 | intron-variant | Rfwd2 | Mm_Celera | 1:159243356 | TCTCACTTATAGACA[A/G]AAATAATGTTAAAAA | 26374 |
rs32337767 | snp | G/T | 0.5 | 0 | intron-variant | Rfwd2 | Mm_Celera | 1:159243223 | AGGAAAGATAATGGG[G/T]TTTTTAAAACGATTT | 26374 |
rs32339079 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159341331 | CTTTTCTAGGATCCC[C/T]TTTTCCTAGGCACAT | 26374 |
rs32348415 | snp | C/G | 0.375 | 0.216506 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159336965 | TTCAGAGTCTTCTTT[C/G]TAGGCTAGGATAATG | 26374 |
rs32360534 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159332728 | CCAAAATAGATCATT[A/G]CCTGTTTCAATATAC | 26374 |
rs32370819 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159269218 | GATGGAAGCTTGAGC[A/T]TTAGGAGTTCAGAAT | 26374 |
rs32377728 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Rfwd2, Scarna3a, Mir1843b | Mm_Celera | 1:159338963 | CTTTTTTAATAATCT[A/G]TGGCTACTTTGAATT | 26374 |
rs32382641 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159303930 | TTTAATTTTCTTTTT[G/T]TATTAGATATTTTCT | 26374 |
rs32386098 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159277259 | TGCCTCTGAGGCCAC[C/T]CTGGTCTATACACAT | 26374 |
rs32441292 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159259278 | CTTTGTAGACCAGCT[A/G]GCCTCAAACTCACAG | 26374 |
rs32484275 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159292123 | CTTATTGTTTGTGTG[C/T]TTGCATTGAATAAGG | 26374 |
rs32493675 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159319693 | ACAGAAACATTTGTT[G/T]TTTTTTTTTTTTAAA | 26374 |
rs32497103 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159310879 | TATTTAAAACCATTT[G/T]TTCCCTGTGTTTTTG | 26374 |
rs32515492 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159267295 | AAATTTAAATTTAGT[G/T]TTTTTTGTATTTACA | 26374 |
rs32524168 | snp | C/T | 0.32 | 0.24 | intron-variant | Rfwd2 | Mm_Celera | 1:159279258 | AGGAATGAATGCATG[C/T]ACTAAATAACATAAA | 26374 |
rs32533801 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159335720 | TCTTTCCTTGTTCAA[A/T]GCCACTCACAGGAGA | 26374 |
rs32538002 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159292227 | TACAATCTAAAAATG[A/G]AGGAGACATCTGTGC | 26374 |
rs32558193 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159281366 | ACTCCCAGTTCCCCC[A/G]CCTCTAAAATTGCAG | 26374 |
rs32561481 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159318404 | TTGAATCAAACCCAG[A/T]TCCTCTACAAGAACA | 26374 |
rs32573091 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159334417 | AATTCAAGCCACTGC[A/G]CAGAGAGGTAGAACA | 26374 |
rs32585681 | snp | A/G | 0.32 | 0.24 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159263123 | ACCTGTTATAAATAA[A/G]CTGTCGGTAGTAGAG | 26374 |
rs32586987 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159248921 | TTTTAGAAGGCACTT[A/G]AATGCTTTCACATGG | 26374 |
rs32589933 | snp | C/G | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159276645 | TTGAGTTTGTTTAGT[C/G]TTGATTGAATGACGT | 26374 |
rs32592038 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159292233 | CTAAAAATGAAGGAG[A/C]CATCTGTGCTAGGCT | 26374 |
rs32602501 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159266944 | CTAAATTTATATTGA[C/T]ATTTATTATAGTAAT | 26374 |
rs32611017 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159314987 | AAGGACCACATCTGC[G/T]CTCGGTCTTTCTGCC | 26374 |
rs32622880 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159274128 | CAAAAACATACACAG[A/T]AAAACTGGTTCATGA | 26374 |
rs32650680 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159269288 | TACATAAGACCTTAC[G/T]TCCAAAAATCAAAAA | 26374 |
rs32651097 | snp | C/G | 0.32 | 0.24 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159322228 | GGTTTGCTACATATG[C/G]CATTTATTATGTTGA | 26374 |
rs32652086 | snp | A/G | 0.32 | 0.24 | intron-variant | Rfwd2 | Mm_Celera | 1:159323433 | TCTTCCTCTGATGTG[A/G]CCCACCTTGCCCTTT | 26374 |
rs32655621 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159327988 | CTCCCAAGTGCTAGG[A/G]TTAAAGGCGTTCACC | 26374 |
rs32655806 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159276475 | TTATTTTATACTCCA[G/T]ATTTTATTCCTCTCC | 26374 |
rs32684457 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159307184 | TATCTGACATGGTTA[C/T]CATTATTACCCACAC | 26374 |
rs32684463 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159238329 | CTGATAGTCTGATCT[C/T]TGCTCTGGAACCGCA | 26374 |
rs32698710 | snp | A/T | 0.32 | 0.24 | intron-variant | Rfwd2 | Mm_Celera | 1:159279369 | TTTGAGTTTGGGGTA[A/T]ACATGACAGTGGAAC | 26374 |
rs32704882 | snp | G/T | 0.32 | 0.24 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159272194 | TCTCATGCCCTCAGG[G/T]CCAGCTCACCAGCAC | 26374 |
rs32717565 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159334297 | GATACCCAAGCCTCT[A/G]CTCTGGCCCTGATGT | 26374 |
rs32725062 | snp | A/G | 0.32 | 0.24 | intron-variant | Rfwd2 | Mm_Celera | 1:159279226 | TAAACTTTTTATGTC[A/G]CAGAACAAACTGTGC | 26374 |
rs32729636 | snp | A/G | 0.32 | 0.24 | intron-variant | Rfwd2 | Mm_Celera | 1:159279370 | TTGAGTTTGGGGTAT[A/G]CATGACAGTGGAACA | 26374 |
rs32730452 | snp | A/C | 0.32 | 0.24 | intron-variant | Rfwd2 | Mm_Celera | 1:159341768 | CTTTTCCCAAAAGTA[A/C]TGGATTATTTTTTTC | 26374 |
rs32732987 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159311185 | TTGTATGTGGTCTAA[A/G]GGTACAACTTTGTTT | 26374 |
rs32733467 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159233424 | ACTTGTAATACTGTT[A/C]ATAATTTTGTAGTCA | 26374 |
rs32740287 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159290676 | AAGAGGGAGTCAGAT[A/C]TTATTATGGATGGTT | 26374 |
rs32754625 | snp | A/T | 0.32 | 0.24 | intron-variant | Rfwd2 | Mm_Celera | 1:159310562 | TTAGTCTTTTAGACT[A/T]GATGTGTCTGCCCAC | 26374 |
rs32757390 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159333646 | AAATAGAAAATAAAA[A/T]TTTAAAATTAATATG | 26374 |
rs32765308 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159333842 | AAAGAGGAAGGCAGC[A/G]TCTTCAACAACTGCT | 26374 |
rs32767003 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rfwd2 | Mm_Celera | 1:159299647 | CTTAAGATTAAAATG[A/G]AAGCTTGCTCTTTTT | 26374 |
rs32783434 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159282971 | TTTACAGTCTTCATT[C/T]CAACTCCCAGCAATG | 26374 |
rs32813722 | snp | A/T | 0.32 | 0.24 | intron-variant | Rfwd2 | Mm_Celera | 1:159306113 | GAATTTATGAAAAAA[A/T]TTTATTGGTAATTTT | 26374 |
rs33851611 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Rfwd2, Scarna3a, Mir1843b | Mm_Celera | 1:159338789 | AAAAATGAGAAAACT[A/G]GTCACTGCTGTCTTG | 26374 |
rs33860007 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rfwd2 | GRCm38.p3 | 1:159333765 | AATGCTGCAGTAATG[C/T]AAACAGTGTGGTTCT | 26374 |
rs33889309 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rfwd2 | Mm_Celera | 1:159301918 | GTGGCTATTTCTGTT[C/T]ATGCCAGTCATCATT | 26374 |
rs45720062 | snp | A/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159235219 | AAAGTAAGTAATTAT[A/T]CTCTTACATTGTATA | 26374 |
rs45842843 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159328489 | CCAGCATCTGAAAGG[C/T]AGAAAGAAACAATTG | 26374 |
rs46143303 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159330778 | TTATTTTCTTCTGTA[C/T]CTTTTAATAATTTTT | 26374 |
rs46302064 | snp | A/C | | | intron-variant | Rfwd2 | Mm_Celera | 1:159255190 | CAGGGCAGAGTGGAG[A/C]TGGGGCTGCTTAGTT | 26374 |
rs46325576 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159318979 | TAACCCCCCCACATA[C/T]TTTTAATATTTGTTA | 26374 |
rs46364827 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159326097 | CATCAGATCCCATTA[A/G]AAATGGTTGTGAGCC | 26374 |
rs46377826 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159328001 | GGATTAAAGGCGTTC[A/G]CCACCACTGCCTGGC | 26374 |
rs46462485 | snp | C/T | | | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159345349 | CGTCCTCTTCTGGGC[C/T]CCTTAAGCACCAGGC | 26374 |
rs46502547 | snp | C/T | | | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159347495 | TTTTACCTTAATCTT[C/T]ATTTCAGGGGTTTTG | 26374 |
rs46534500 | snp | G/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159243219 | AAGGAGGAAAGATAA[G/T]GGGTTTTTTAAAACG | 26374 |
rs46537740 | snp | C/G | | | intron-variant, upstream-variant-2KB | Rfwd2 | Mm_Celera | 1:159256771 | TTTCAGCTAGCAAGT[C/G]TCAAGTTGCCTTCCA | 26374 |
rs46582058 | snp | G/T | | | utr-variant-3-prime | Rfwd2 | GRCm38.p3 | 1:159345817 | GGCCATATGGTCTCT[G/T]ATAACTGTTAGAGAA | 26374 |
rs46632627 | snp | A/T | | | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159347568 | TAATGTGAATAAAAA[A/T]TTGAAGTTTGTATTA | 26374 |
rs46691073 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159318361 | TACATTAATTGCCTA[C/T]TTTAAAAATCAATAT | 26374 |
rs46920713 | snp | G/T | | | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159345222 | TTCTGGCTGGGGCTG[G/T]AGAGAGGCTCAGAGA | 26374 |
rs46976907 | snp | C/G | | | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159345122 | AACAAAAAGTTTATT[C/G]AGCCACAGCTGAGCT | 26374 |
rs47004011 | snp | A/G | | | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159346336 | CCCAACAAAACTAAA[A/G]CAATGGTACATGTCC | 26374 |
rs47126982 | snp | C/T | | | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159345252 | AATAAGAGCACTGGT[C/T]GCTCCTACAGAGGAT | 26374 |
rs47127080 | snp | C/T | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159309279 | TGGAGTGCTTATGCG[C/T]GTGTATATACAGAAG | 26374 |
rs47176786 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159323123 | ATACTGGATAATTCA[A/G]TATCTTAAAATGTAC | 26374 |
rs47214054 | snp | C/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159337640 | TACTGGTAATTAAAT[C/G]CTCTATTTAGTTTCA | 26374 |
rs47374594 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rfwd2 | Mm_Celera | 1:159257069 | AGTTTTCTCAGTTGA[A/G]AATCCCTCTCTGCAA | 26374 |
rs47414302 | snp | A/G | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159316974 | GGTGTTTTGCCTGCA[A/G]GAAAGTGCACCTCAT | 26374 |
rs47477132 | snp | A/G | | | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159347571 | TGTGAATAAAAAATT[A/G]AAGTTTGTATTACTT | 26374 |
rs47504068 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159255486 | CTTTTCTCGGGTAGC[C/T]GATATTTTGTAATAG | 26374 |
rs48145649 | snp | A/C | | | intron-variant | Rfwd2 | Mm_Celera | 1:159251799 | ACTCTGTAGACCAGG[A/C]TGGCCTGAACTCAGA | 26374 |
rs48206688 | snp | C/T | | | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159347174 | AAACTCAGTTTTACT[C/T]TGTAGTCACAAGTAG | 26374 |
rs48262221 | snp | A/G | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159233714 | TTGATATTACTGGTA[A/G]GATTATGAGAGCTTA | 26374 |
rs48320213 | snp | A/G | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159312966 | CCTGTGCATGTTAGG[A/G]CAGACGCTGGGAATT | 26374 |
rs48334796 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159251837 | CTGCCTCCGCCTCCC[A/G]AGTGCTGGGATTAAA | 26374 |
rs48374632 | snp | A/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159251820 | TGAACTCAGAAATCC[A/T]CCTGCCTCCGCCTCC | 26374 |
rs48414400 | snp | G/T | | | utr-variant-3-prime | Rfwd2 | GRCm38.p3 | 1:159345140 | CCACAGCTGAGCTAG[G/T]AACACCTTTTTGTCA | 26374 |
rs48422688 | snp | G/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159330790 | GTACCTTTTAATAAT[G/T]TTTTGCTAGATAAAA | 26374 |
rs48431021 | snp | A/G | | | upstream-variant-2KB | Rfwd2 | Mm_Celera | 1:159231568 | ATACTCTTGCAGTTT[A/G]CAGCAAGACTGTTTC | 26374 |
rs48461010 | snp | A/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159243218 | GAAGGAGGAAAGATA[A/T]TGGGTTTTTTAAAAC | 26374 |
rs48559654 | snp | A/C | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159272084 | CTGCCAGCTTCCTGC[A/C]CAAGCACCCACTGGT | 26374 |
rs48693004 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159333053 | GAGTAGGACTGGAAA[A/G]AGCAAAGAACAGCAT | 26374 |
rs48758320 | snp | C/T | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159313521 | TAAAGGCATGCACCA[C/T]CATAACCCATCCTAT | 26374 |
rs48916654 | snp | A/C | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159330078 | TGCCATAGAGGCAGA[A/C]ATAGTGAGATCCCTG | 26374 |
rs48971027 | snp | A/T | | | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159345860 | CCAGGGTATCAGGGA[A/T]GTAGCTACTATCGTT | 26374 |
rs49020032 | snp | G/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159265953 | TATTTAACCAATAGC[G/T]TTATATTGGGGAGCA | 26374 |
rs49116434 | snp | C/T | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159333063 | GGAAAAAGCAAAGAA[C/T]AGCATAGTAAAAGTC | 26374 |
rs49136709 | snp | C/T | | | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159345251 | GAATAAGAGCACTGG[C/T]CGCTCCTACAGAGGA | 26374 |
rs49274772 | snp | C/T | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159332964 | TGGAGACATTCAGCA[C/T]GTGCAAGCCAGTAAC | 26374 |
rs49580560 | snp | A/C | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159233617 | CGACACAGTAGAATT[A/C]AGGCATTTGGCATCT | 26374 |
rs49640308 | snp | C/T | | | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159347488 | AATTATGTTTTACCT[C/T]AATCTTTATTTCAGG | 26374 |
rs49743518 | snp | A/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159287865 | TATTTTCTTCAAAAA[A/T]TTTTTTATTATAATT | 26374 |
rs49788846 | snp | C/T | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159237498 | ACTTGTGGGGTTGGA[C/T]GGGGTACAGTCACAA | 26374 |
rs49865317 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159243630 | CTACTTCACAAAGTC[A/G]TCCTTTGACCCCTGG | 26374 |
rs49871493 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159237200 | ACCAGGAGAGGATAT[C/T]GAATACCATTTCAGA | 26374 |
rs49978409 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159251826 | CAGAAATCCACCTGC[C/T]TCCGCCTCCCAAGTG | 26374 |
rs50143080 | snp | A/T | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159324081 | ACACTGATTTCTTAC[A/T]AGAAATCATGTTCTG | 26374 |
rs50158619 | snp | A/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159243228 | AGATAATGGGTTTTT[A/T]AAAACGATTTCTATA | 26374 |
rs50263462 | snp | A/G | | | utr-variant-3-prime | Rfwd2 | GRCm38.p3 | 1:159345663 | GATCAAGTAAACAGG[A/G]AAGGACTGTCCTTAC | 26374 |
rs50323614 | snp | A/T | | | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159345396 | TTCAAAGATCCAGAT[A/T]CAACGCTCACACATA | 26374 |
rs50364172 | snp | C/T | | | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159347252 | TATAATCATGTGTCC[C/T]CCCTCCCAGTTTTAA | 26374 |
rs50406865 | snp | C/T | | | downstream-variant-500B | Rfwd2 | Mm_Celera | 1:159347729 | TTCTCAACAGCAGAG[C/T]GCAGTCTAGACCACC | 26374 |
rs50424063 | snp | A/G | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159333113 | CCAACATTACCTACC[A/G]TAAATGGGAAAATCA | 26374 |
rs50469101 | snp | C/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159330779 | TATTTTCTTCTGTAC[C/G]TTTTAATAATTTTTT | 26374 |
rs50515528 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159251829 | AAATCCACCTGCCTC[C/T]GCCTCCCAAGTGCTG | 26374 |
rs50799656 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159235207 | ATACATAAAATAAAA[A/G]TAAGTAATTATACTC | 26374 |
rs50850010 | snp | A/G | | | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159347514 | TCAGGGGTTTTGTAG[A/G]GTTTCTTACACAACT | 26374 |
rs50850370 | snp | A/G | | | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159347515 | CAGGGGTTTTGTAGG[A/G]TTTCTTACACAACTT | 26374 |
rs50984068 | snp | A/G | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159247608 | GAAGGCTAGATGTGA[A/G]TTGCTGCGTGGGTGC | 26374 |
rs51016677 | snp | C/T | | | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159347223 | CCTGTCGCCCCACCC[C/T]GGGGCTGCTGGGATA | 26374 |
rs51049908 | snp | A/C | | | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159346345 | ACTAAAGCAATGGTA[A/C]ATGTCCAACATAAAC | 26374 |
rs51104927 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159289800 | GCTACAGAGAAACCC[C/T]GTCTCGGGAAAAAAA | 26374 |
rs51118725 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159255465 | TTCCTTGTGGTTTTG[A/G]CAGGTCTTTTCTCGG | 26374 |
rs51265249 | snp | A/C | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159233958 | TTCACTAATATAATT[A/C]GTAATTTTGCTTTTG | 26374 |
rs51431610 | snp | C/T | | | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159346560 | TGCTAAACTTAATGG[C/T]CTCAAGTCTGAGAGA | 26374 |
rs51467143 | snp | A/G | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159246449 | TGAACACTTGTAATC[A/G]GCCAGCACTTCAGAT | 26374 |
rs51529414 | snp | A/G | | | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159345138 | AGCCACAGCTGAGCT[A/G]GGAACACCTTTTTGT | 26374 |
rs51583455 | snp | A/C | | | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159347155 | TTACCATGTAGCACA[A/C]ACCAAACTCAGTTTT | 26374 |
rs51691647 | snp | A/T | | | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159345556 | TTAATGTTTACAATT[A/T]AAAAAAAATAATAAG | 26374 |
rs51750569 | snp | A/C | | | intron-variant | Rfwd2 | Mm_Celera | 1:159333203 | TACAGTGCTCAAATT[A/C]GTGAGTCAGGAGAAA | 26374 |
rs51767045 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159243488 | AGAGTGTGTGTGTGT[A/G]TGTGTATTATTTATT | 26374 |
rs51827357 | snp | A/T | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159262956 | CCTTTAGAAATAGTA[A/T]ACCTTGAGCTATGGT | 26374 |
rs51975889 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159337662 | TTAGTTTCATATGAA[A/G]TTGAGTTTCTAGGGA | 26374 |
rs52038113 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159325625 | GGTTCCATATTTTGT[C/T]TATTCCTCTCATAAT | 26374 |
rs52096017 | snp | C/T | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159280730 | CTTAATGTGTGTGCG[C/T]GTGTGCCTGCCTGTC | 26374 |
rs52231457 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159250642 | TCATACACACACACA[C/T]ACACACACACACACA | 26374 |
rs52337991 | snp | C/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159280821 | TGTCTGTGTCTGTGT[C/G]TGTGTCTGTGTGTCT | 26374 |
rs52364420 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159251760 | ACAGGGTTTCTCTGT[A/G]TAGCCCTGGCTGTCC | 26374 |
rs52401435 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159237039 | GTGTGTGTATATATA[C/T]ATACACACACACACA | 26374 |
rs52449372 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159268352 | CGAGACAGGGTTTCT[C/T]TGTATAGCCCTGGCT | 26374 |
rs52451472 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159236987 | TCTATAGCATGCATG[C/T]ACATGCATATATGCA | 26374 |
rs52475521 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159237041 | GTGTGTATATATATA[C/T]ACACACACACACACA | 26374 |
rs52479201 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159259201 | CTTTTTTCCCCCTTT[C/T]CCTTTCTATTTCCTA | 26374 |
rs52493441 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159259197 | TTCTCTTTTTTCCCC[C/T]TTTTCCTTTCTATTT | 26374 |
rs52525590 | snp | A/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159275709 | TATTGTATAACTGAA[A/T]TTTATTTGTGTTTGA | 26374 |
rs52554843 | snp | C/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159280809 | TCTCTCTCTCTGTGT[C/G]TGTGTCTGTGTCTGT | 26374 |
rs107767272 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159325610 | TCTAACACTAGGGGT[A/G]GTTCCATATTTTGTT | 26374 |
rs107953339 | snp | C/T | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159303110 | ggaggaatgaagtat[C/T]catatgttggtcttc | 26374 |
rs108250736 | snp | C/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159280805 | TCTCTCTCTCTCTCT[C/G]TGTCTGTGTCTGTGT | 26374 |
rs108298983 | snp | C/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159250690 | ACACACACACACACA[C/G]ACAGAGAGAGAGAGA | 26374 |
rs108325908 | snp | C/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159250692 | ACACACACACACACA[C/G]AGAGAGAGAGAGAGA | 26374 |
rs108378358 | snp | G/T | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159303073 | GTAACTACTTCCATG[G/T]GTATTTTGTTCCCTA | 26374 |
rs108857189 | snp | A/G | | | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159346671 | CTACTTAGAACCCCA[A/G]TTCCAAAGAATCTGA | 26374 |
rs108902276 | snp | C/T | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159261608 | GTGTGTGTGTGTGTG[C/T]GCGCGCGCGCGTATA | 26374 |
rs108906437 | snp | C/T | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159303080 | CTTCCATGGGTATTT[C/T]GTTCCCTATTCTAAG | 26374 |
rs108933507 | snp | C/T | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159303326 | AGCTGAGTAGTACTC[C/T]ATTGTGTAGATGTAC | 26374 |
rs211696980 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159295480 | CATGCTAGGAAAGCA[C/T]TGTGCTAACTGAGCT | 26374 |
rs211734131 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159238694 | GTAGAACACCAGGAT[A/G]GCCTCAAACTCACAG | 26374 |
rs211770411 | snp | A/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159249831 | TTATACTTGGTTAGC[A/T]AAATTTATTCAAAGT | 26374 |
rs211772248 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Rfwd2 | Mm_Celera | 1:159257637 | TTTGTAGCTTTTCCA[-/T]TTTTTTTGTGGCTTA | 26374 |
rs211780154 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159305242 | GAAGTGGTGTTTACA[A/G]TCTTGCTCTCTATAG | 26374 |
rs211806690 | snp | A/C | | | intron-variant | Rfwd2 | Mm_Celera | 1:159238257 | AGCGAACAATGACAC[A/C]GTTTACTTCAGGAGC | 26374 |
rs211816946 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159293098 | AGAGTGCTCAGAGCT[A/G]GAGAAGTGACCCAAG | 26374 |
rs211821226 | snp | C/T | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159283373 | GTGAGCCTTCCAATT[C/T]TGGATTGTAGTCATT | 26374 |
rs211857816 | snp | G/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159284118 | TTTTTTTGTTTGTTT[G/T]TTTTTTTTAACCTTT | 26374 |
rs211892441 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159284860 | TCCAGAATGTTTTAT[C/T]GTTCCAGAGCAAGCT | 26374 |
rs211892446 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159274763 | AATACTAGGTTCCCT[A/G]CTCAGCATATGTATT | 26374 |
rs211992550 | snp | A/C | | | intron-variant | Rfwd2 | Mm_Celera | 1:159325317 | AAGTAATATTTGGTG[A/C]AATAGAGAGAAAAAA | 26374 |
rs211999668 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159268459 | ATTAAAGGCGTGAGC[C/T]ACCACGCCCGGCTTT | 26374 |
rs212016432 | in-del | -/A/AA | | | intron-variant | Rfwd2 | Mm_Celera | 1:159280130 | ATAATAAATAAATTG[-/A/AA]AAAAAAAAAGAATTC | 26374 |
rs212026672 | snp | G/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159342747 | GATGAAAAGAATCTA[G/T]TCTCTTCAACTGCCC | 26374 |
rs212035696 | snp | G/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159291971 | AGCATAGTAAGCTTA[G/T]AAAGGAAAAATACAA | 26374 |
rs212067533 | in-del | -/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159248106 | GGATCATTTCATTAA[-/T]TTTTGAAGCATCTAA | 26374 |
rs212078797 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159333658 | AAATTTTAAAATTAA[C/T]ATGGTAACAAAAAAG | 26374 |
rs212137233 | snp | C/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159261211 | TTTTGTTCTCTATTT[C/G]TGTGGAAGATCATTA | 26374 |
rs212138154 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159325898 | AGTAGCTAAAGTGTA[A/G]TCACTCTTTAGAATA | 26374 |
rs212147458 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159251040 | CCTAATAAATCCCCT[C/T]TTGCTTTAATGTCTT | 26374 |
rs212156764 | in-del | -/ATACACACAT | | | intron-variant | Rfwd2 | Mm_Celera | 1:159317652 | CATACACACACATAC[-/ATACACACAT]ACACACATATATATC | 26374 |
rs212161961 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159260406 | CCTTTTACTTCTGCT[C/T]AGAGATTCCTTTTGC | 26374 |
rs212182935 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159317006 | CATATAGTACCCTCA[C/T]AGGTCCAAAGCTGTG | 26374 |
rs212218900 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159318175 | ACCTGGTCAAGGGAT[C/T]ATTGGATCGTGGTAG | 26374 |
rs212224856 | snp | C/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159267757 | GAGATTTGACTGTTG[C/G]AATCCAGTCACCATC | 26374 |
rs212239114 | in-del | -/A | | | intron-variant | Rfwd2 | Mm_Celera | 1:159337716 | GAGGCAGGAATTTTT[-/A]AAAAAAAAGTATGGG | 26374 |
rs212242444 | snp | A/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159280484 | CCTACAGTTAAAGAG[A/T]GAATTGTTATACTGT | 26374 |
rs212273727 | snp | A/T | | | upstream-variant-2KB | Rfwd2 | Mm_Celera | 1:159231059 | TTTAGATAAGTGACA[A/T]CAGGGACAAGAAGCA | 26374 |
rs212304729 | snp | A/G | | | downstream-variant-500B | Rfwd2 | Mm_Celera | 1:159347728 | attctcaacagcaga[A/G]tgcagtctagaccac | 26374 |
rs212325116 | in-del | -/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159247316 | TAGTACTTCATTAAC[-/T]TTTTATTTTCATTTT | 26374 |
rs212330989 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159261677 | TCTAGAAGTCAGATG[A/G]CAACTGCATGTATCA | 26374 |
rs212367984 | snp | G/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159326869 | GTTTTTACAGTGTTG[G/T]GTTCATTTAATTCTA | 26374 |
rs212424288 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159286058 | CATATTTGATTTGAG[A/G]TTAAGATGTGGTTTT | 26374 |
rs212440435 | in-del | -/AA | | | intron-variant | Rfwd2 | Mm_Celera | 1:159273627 | TAGCCTAAAGGGATT[-/AA]AAAAAATCCATTTTG | 26374 |
rs212463827 | in-del | -/A | | | intron-variant | Rfwd2 | Mm_Celera | 1:159303904 | AAGGTAATTTCAATT[-/A]AAAATTTTTTTTTAA | 26374 |
rs212498346 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159344139 | AGCATTGACCTGACA[C/T]GTCAAGGGACCTTTA | 26374 |
rs212553117 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159329998 | AGTTGGGTTAAGCAT[A/G]AGGACCTGAGTTAGA | 26374 |
rs212568002 | snp | A/C | | | intron-variant | Rfwd2 | Mm_Celera | 1:159311508 | CAGTCAGCCCCACTC[A/C]CTCAGTCCCTGCTTC | 26374 |
rs212593249 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159321509 | TACCTCAGTACAAAG[C/T]TGGAAGCAGAGTTGT | 26374 |
rs212600809 | snp | A/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159299700 | AGAATATCTTTTTTT[A/T]AATTAAAATTTAAAA | 26374 |
rs212609369 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rfwd2 | Mm_Celera | 1:159256744 | GCAACTGGGGTGGGG[C/T]GGGAGGGTTTATTTC | 26374 |
rs212611179 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159246466 | CCAGCACTTCAGATG[A/G]TGATATAGGGGATTT | 26374 |
rs212612080 | in-del | -/AA | | | intron-variant | Rfwd2 | Mm_Celera | 1:159337715 | GAGGCAGGAATTTTT[-/AA]AAAAAAAAAGTATGG | 26374 |
rs212621678 | in-del | -/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159269992 | GAGATCCTAGTTGTC[-/T]TAACAGTTAGAAGTA | 26374 |
rs212648162 | snp | A/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159256106 | GACTAGTGAGAGGGT[A/T]GGCGCTTTAGTGTCT | 26374 |
rs212660818 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159344241 | CCTAAAATTACAATG[C/T]CCATGAAACAATCCT | 26374 |
rs212731924 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159235266 | TTATGAAAACATCCA[A/G]TGAGTATTTGTGGCT | 26374 |
rs212746634 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159286856 | GCTGAACCAACAAAA[C/T]CCAAGCCTTCTTTAT | 26374 |
rs212770843 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159247294 | TCTTTCTATCATATT[A/G]TAGGCTATAGTACTT | 26374 |
rs212785549 | snp | A/C/G | | | utr-variant-5-prime | Rfwd2 | Mm_Celera | 1:159232327 | TTGTTCCCCCGGCCC[A/C/G]TCTCCCGGCGCGTCC | 26374 |
rs212800559 | in-del | -/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159242773 | GATAATAATCATCTC[-/T]TTTTTTCTCCTAAGA | 26374 |
rs212817113 | in-del | -/ACAA | | | intron-variant | Rfwd2 | Mm_Celera | 1:159336613 | ATTTTGAACAAACAG[-/ACAA]ACAAACAAATAGGAA | 26374 |
rs212821761 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159290086 | AAGTTTATTATACCC[A/G]CAGAAGAAATGAAGA | 26374 |
rs212857606 | snp | A/C/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159272244 | CTACTGTGCTGCCTT[A/C/G]GTCCTGGAGGTACAG | 26374 |
rs212860493 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159281475 | AAGACCCTATCTGCT[A/G]CCCACCCACTGTCCC | 26374 |
rs212862037 | snp | A/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159290842 | TTGGTTTGAAATTGC[A/T]TATTTTAAACTATCT | 26374 |
rs212867514 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159320695 | CTCATGTTGATGCGT[A/G]TTGTGTACATGCTAG | 26374 |
rs212897434 | snp | A/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159282456 | TTAAAATACAATTCC[A/T]TAATTTTCTTCTTCT | 26374 |
rs212904662 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159264240 | TAAAAATATTTAAGA[A/G]GTGCCCATGAGAGCA | 26374 |
rs212949134 | snp | A/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159313745 | TGTGTGTTATATACA[A/T]TTTTTTTTTTTTTTT | 26374 |
rs212950091 | snp | C/G | | | downstream-variant-500B | Rfwd2 | Mm_Celera | 1:159347834 | CAGAGGAGCCCAATA[C/G]AATGGCACTTTTAGC | 26374 |
rs212953955 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159269539 | TGCTTAAAATATTCA[A/G]TACGGGCAACAGCCA | 26374 |
rs213053273 | in-del | -/CTGC | | | intron-variant | Rfwd2 | Mm_Celera | 1:159287488 | CTAGATGAATTTTGA[-/CTGC]CTAAATCTGAGCATT | 26374 |
rs213057176 | in-del | -/GGCTCACA | | | intron-variant, upstream-variant-2KB | Rfwd2, Scarna3a, Mir1843b | Mm_Celera | 1:159339069 | GAAAAGATATATTTT[-/GGCTCACA]GGCTTAGAGATTGCA | 26374 |
rs213080986 | in-del | -/A | | | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159347363 | ACCCCTTAGTTAGAT[-/A]TTTTTTTTTCCTTTT | 26374 |
rs213084824 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159236065 | TTAACTGTAGGGTTG[A/G]TTGACATTTTAGATA | 26374 |
rs213100271 | snp | G/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159332562 | CCCCGATTAGTTCCC[G/T]TTGTTTCCTACAACA | 26374 |
rs213143712 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159266623 | CTTTGCACTTAGTGG[C/T]CAGTTTAGTCGGCCT | 26374 |
rs213144728 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159323514 | AGTTTCTTTTTGAAA[A/G]TTTCATTTGCATGGA | 26374 |
rs213151398 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159300673 | TAATATTAGCACTTA[C/T]TGCTTTAGGAGAAAG | 26374 |
rs213185564 | snp | A/C | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159324320 | CCATCCCTCAGCACC[A/C]GGGTGAGTTCAGAAT | 26374 |
rs213185656 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159313871 | TCTGTGATCCCCTTA[A/G]ATTGACAGTACTTTG | 26374 |
rs213204121 | snp | C/G | | | intron-variant, upstream-variant-2KB | Rfwd2 | Mm_Celera | 1:159257749 | TTGTGCCCTTTGATA[C/G]CCAGGTTTCTAATAA | 26374 |
rs213217462 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159314698 | ACCCAACTATCTGAC[A/G]CTTGTCTTTTTTTCC | 26374 |
rs213222248 | snp | G/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159249175 | ACAAAAATACAAATT[G/T]TGTGTGCTTTTTACC | 26374 |
rs213281132 | in-del | -/ACTTAAGCTA | | | intron-variant | Rfwd2 | Mm_Celera | 1:159254423 | TCTAGCCCACATAGT[-/ACTTAAGCTA]ACTTAAGCTATTGGT | 26374 |
rs213365141 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159341108 | TCAAAGTTTGGGTGG[A/G]AGGATAGGAGAAAAG | 26374 |
rs213381188 | snp | A/C | | | intron-variant | Rfwd2 | Mm_Celera | 1:159344097 | ATTCTCAGAAGGAAA[A/C]CTAAATTGTTGGTTT | 26374 |
rs213384256 | in-del | -/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159286923 | GCTAAAATAAGTACC[-/T]TTTTTTGTAGGTTTG | 26374 |
rs213387956 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159285907 | TAAAAAAGGAAAAAT[A/G]AGCATGGTGTGCTTG | 26374 |
rs213392173 | in-del | -/TTTTTATTA | | | intron-variant | Rfwd2 | Mm_Celera | 1:159341978 | TGCGGGTTTTTTTTT[-/TTTTTATTA]TTATTTTTCTATTAG | 26374 |
rs213412933 | snp | A/C | | | intron-variant | Rfwd2 | Mm_Celera | 1:159331704 | CCTCTTTCACCGAGG[A/C]CAGACAAGGAGGCCC | 26374 |
rs213424096 | snp | A/C | | | intron-variant | Rfwd2 | Mm_Celera | 1:159336174 | AAGTTCTATGAGCCC[A/C]GATATTGGGAATACT | 26374 |
rs213433246 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159265923 | TTCACTCAAGTAATT[A/G]GCTTTAGCTACTTTT | 26374 |
rs213448928 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159272842 | GAGAGGAACAACACC[A/G]TCCCTCTTTTAGCTA | 26374 |
rs213453963 | snp | A/C | | | intron-variant | Rfwd2 | Mm_Celera | 1:159287488 | CTAGATGAATTTTGA[A/C]TGCCTAAATCTGAGC | 26374 |
rs213468816 | in-del | -/GA | | | intron-variant | Rfwd2 | Mm_Celera | 1:159270003 | TGTCTAACAGTTAGA[-/GA]AGTACATAAGCTAAA | 26374 |
rs213473222 | snp | A/C | | | intron-variant | Rfwd2 | Mm_Celera | 1:159276746 | GAAAGGTTTTCGACT[A/C]TATGATTGAACACAT | 26374 |
rs213525472 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159327333 | TTCTTTTCTAGCCAT[A/G]CTGGGGAGAATTAGT | 26374 |
rs213530593 | in-del | -/T | | | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159344913 | GAGAAGAAAAAGAAA[-/T]GGCATGTAATGTCTC | 26374 |
rs213559119 | snp | A/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159328091 | AAATGCAGTTTAGGA[A/T]TCTTGTTTCAGTAAG | 26374 |
rs213561728 | snp | G/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159261820 | CACTTTGTCTCTCTT[G/T]TGTTTAGACCTAAGG | 26374 |
rs213582575 | in-del | -/A | | | intron-variant | Rfwd2 | Mm_Celera | 1:159254319 | GTCTCACTGGAACTG[-/A]ATTTACAGGTGGTTG | 26374 |
rs213604263 | in-del | -/AC | | | upstream-variant-2KB | Rfwd2 | Mm_Celera | 1:159230858 | CATCATCAGACTGGT[-/AC]AGACATCAGACACGT | 26374 |
rs213621141 | snp | A/G | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159262458 | ATGATAGTGTCAGGA[A/G]TCTTCCTTCCACAGT | 26374 |
rs213621343 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159252859 | GTTTCTCTGTATAGC[C/T]CTGGCTGTCCTGGAA | 26374 |
rs213671743 | in-del | -/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159332481 | TAAGTATAAAATTGC[-/T]TTTTAGCATCCCCCC | 26374 |
rs213671938 | snp | G/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159273973 | GAAAATGGAATGCAG[G/T]AGTGGCTATACTATG | 26374 |
rs213734859 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159309244 | AGTACGTATGTGTCT[A/G]TGTGCTTATATGCCT | 26374 |
rs213795553 | snp | A/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159287253 | CTTAGTAGAAGGATT[A/T]CAAATGAAGATACAC | 26374 |
rs213796110 | in-del | -/TT | | | intron-variant | Rfwd2 | Mm_Celera | 1:159306796 | TGACATTATTGTATA[-/TT]TTTTTCCATGAGACT | 26374 |
rs213799247 | snp | A/G/T | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159343757 | AACTGCATTGTTAGC[A/G/T]AGGCACACTAATTCA | 26374 |
rs213826188 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159287866 | ATTTTCTTCAAAAAT[C/T]TTTTTATTATAATTA | 26374 |
rs213832041 | snp | C/T | | | upstream-variant-2KB | Rfwd2 | Mm_Celera | 1:159230996 | TTGCTGCTTCAATGC[C/T]AACAAAGACGGAGTT | 26374 |
rs213850943 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159233041 | AAGTGGTGAAATGGG[A/G]TTGCACAGAAGTGGG | 26374 |
rs213862487 | snp | A/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159278951 | TTCTTGGCATCCACA[A/T]TAGTGCCTGGGTTTG | 26374 |
rs213869880 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159275891 | AAATTTCTTTCTCCT[A/G]TGCCATTTTGATATC | 26374 |
rs213894018 | snp | C/T | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159242309 | ATCTGTGCCTTCCAC[C/T]CTGGCAACCAGTAAT | 26374 |
rs213937141 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159322012 | TTGGGTTATATACCT[A/G]GAGAAAGCACCCACT | 26374 |
rs213981111 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159279760 | CTCAGTTATCTCATG[A/G]CTGTTCTTATTTTGC | 26374 |
rs214002733 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159269602 | TTTTAATAAACATCC[C/T]AAAGGCCAGATGTGT | 26374 |
rs214009858 | snp | G/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159269661 | ATGCTTGCTGTCCTT[G/T]GCAACAGGGCTGGGG | 26374 |
rs214083133 | snp | A/C | | | intron-variant | Rfwd2 | Mm_Celera | 1:159318400 | TCTCTTGAATCAAAC[A/C]CAGTTCCTCTACAAG | 26374 |
rs214158245 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159302364 | CCAGTAGGGGTGAAG[C/T]GTCTATGTCAGTACT | 26374 |
rs214163397 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159337792 | TGCTAAATAGTTCTC[C/T]AATAATTCCACTAAC | 26374 |
rs214170959 | in-del | -/TCACA | | | intron-variant | Rfwd2 | Mm_Celera | 1:159309134 | GAATGTACAGCCTTT[-/TCACA]TCACAGTAATGCTTT | 26374 |
rs214187365 | in-del | -/TTTTTTTT | | | intron-variant | Rfwd2 | Mm_Celera | 1:159242592 | TCAAAAATTTACTTA[-/TTTTTTTT]TTTTTTTAGTGCTTC | 26374 |
rs214192385 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159292075 | TGGCATGAAGGGCGT[A/G]GTGACTAAAGGGCAA | 26374 |
rs214229354 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159311345 | ACTTCATTGAGTTTT[A/G]TTCATTAATATTTCT | 26374 |
rs214247330 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159270736 | GTCTGTGTGTTTATG[C/T]CTGTGTGATGTAGAT | 26374 |
rs214331902 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159310488 | AAGATTTAATGTATA[A/G]TGGTAATAGTGCCTA | 26374 |
rs214333905 | snp | A/C | | | intron-variant | Rfwd2 | Mm_Celera | 1:159332883 | TAAAATTTCAGTATA[A/C]AATACTTCAAAACAA | 26374 |
rs214342661 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159233962 | CTAATATAATTCGTA[A/G]TTTTGCTTTTGTTTA | 26374 |
rs214352527 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159266754 | CCTTTCTTTAATCTA[C/T]AGCAATTGGAGCAGA | 26374 |
rs214379580 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159298224 | AATTTATGGGACTCT[A/G]TCAGTCAGGGAATAA | 26374 |
rs214448101 | snp | G/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159238171 | CTTAGTGACAGTTTG[G/T]CTTCTATTATGGATT | 26374 |
rs214453477 | in-del | -/TT | | | intron-variant | Rfwd2 | Mm_Celera | 1:159263210 | ATATATTTTCTTTGA[-/TT]TTTTTTTTTTACACT | 26374 |
rs214470340 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159333407 | ACAAGTAGCCGTAAA[A/G]TAAATAAAATGTCTA | 26374 |
rs214498491 | in-del | -/TATATA | | | intron-variant | Rfwd2 | Mm_Celera | 1:159265974 | TGGGGAGCAAGATTT[-/TATATA]ATACAACACAGGCTG | 26374 |
rs214504251 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159325254 | TATGCTTATAATTTA[A/G]TAACATTTGAACTTC | 26374 |
rs214507004 | in-del | -/TT | | | intron-variant | Rfwd2 | Mm_Celera | 1:159312324 | TCTATAGACTGATGA[-/TT]TTTTTTTCTTCTTGG | 26374 |
rs214508122 | snp | G/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159267717 | AGAGTGACAGACATA[G/T]TCTCGGTTTTTGTCA | 26374 |
rs214533382 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159325855 | AAGGGAGTTATGTGG[A/G]TAATTAATTAATGAG | 26374 |
rs214534676 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159261082 | GGGATTAAAGGCATG[C/T]GCCACCACACCCGGC | 26374 |
rs214548795 | snp | A/G | | | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159345929 | TCAAACTCTATCTGC[A/G]GCTCATCTGCAATGC | 26374 |
rs214609704 | in-del | -/ATA | | | intron-variant | Rfwd2 | Mm_Celera | 1:159344361 | TATTTTTATGGCATG[-/ATA]ATAACATCAAAATCT | 26374 |
rs214626836 | in-del | -/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159255217 | GTTTGGAACATCCAG[-/T]GGATTTGTGTCACAT | 26374 |
rs214656665 | in-del | -/ATGTT | | | intron-variant | Rfwd2 | Mm_Celera | 1:159299565 | CGTACACCTTCTTAA[-/ATGTT]ATGTTTAGGAAATCT | 26374 |
rs214670569 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159271253 | GGAGAGATGGCTAAG[A/G]GGTTAAGAGCACTAA | 26374 |
rs214684056 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159342655 | TTTTTTTTTTGAAAT[A/G]TATTTATAAAGACAG | 26374 |
rs214718857 | snp | G/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159284099 | TTTTCTCTCTGTTTT[G/T]TTTTTTTTTTGTTTG | 26374 |
rs214725296 | snp | C/T | | | upstream-variant-2KB | Rfwd2 | Mm_Celera | 1:159230242 | TACCAGTAAGCCAGC[C/T]CATCCATATTTGTCT | 26374 |
rs214733084 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159294542 | TTTTTCACAGAATTG[A/G]TTTAAACCAGTGGTT | 26374 |
rs214750365 | snp | A/C | | | intron-variant | Rfwd2 | Mm_Celera | 1:159313714 | ATCTTCTACATTCTT[A/C]TTGTTCTTCAAAGTA | 26374 |
rs214771857 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159295218 | TTTCTACATTTAAGA[A/G]TGTTAAAAACAAGAT | 26374 |
rs214771975 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159284992 | AAAGATGGAAGAATT[A/G]ACTCTTAATTATCAT | 26374 |
rs214796495 | in-del | -/C | | | intron-variant | Rfwd2 | Mm_Celera | 1:159272744 | TGCCTATGCTTTTTT[-/C]CCCCTAACATAAACA | 26374 |
rs214806741 | in-del | -/CATGACATTATTATTATTATATTGTATTTATAGTTTTATGATAGTGTTGTTTTTCTAAGCAACTTTTTTATTTATAA | | | intron-variant | Rfwd2 | Mm_Celera | 1:159341547 | TATTTATAGTTTTAC[lengthTooLong]GATAGTGTTGTTTTT | 26374 |
rs214818137 | snp | A/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159270391 | GGTCTGCATGGTGAG[A/T]CCCTGTGTCTCACCA | 26374 |
rs214863250 | snp | G/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159337725 | ATTTTTAAAAAAAAA[G/T]TATGGGGAGCATATT | 26374 |
rs214865752 | in-del | -/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159318375 | CTTTAAAAATCAATA[-/T]TTTTTTTCCTCTCTT | 26374 |
rs214872972 | snp | C/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159277668 | GATCTAGAGATAGAT[C/G]ATCTAGAGATAGATA | 26374 |
rs214902590 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159329275 | GGGACAGAGTTGGGC[C/T]GGACAATGGAGCTTT | 26374 |
rs214930916 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159264102 | GTGATATGGGTTATC[C/T]ATGTTGATACGGGTT | 26374 |
rs214937490 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159329943 | GAGAAGAGAAGAGAG[A/G]CCGTGTAGAGGGAAG | 26374 |
rs214971700 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159263454 | ATGATTCTTCCTTTG[A/G]AGGTTATAATGCCTA | 26374 |
rs214994107 | in-del | -/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159261904 | TTAGTCCTTTTTTGA[-/T]TTTTTTTTGTTATTG | 26374 |
rs215012368 | snp | A/C | | | intron-variant | Rfwd2 | Mm_Celera | 1:159342103 | CCTCCATTCTCTCTC[A/C]ATTTACTTACACTTT | 26374 |
rs215015175 | in-del | -/TATTTC | | | upstream-variant-2KB | Rfwd2 | Mm_Celera | 1:159230592 | CTATATTGCGTGGAT[-/TATTTC]ACGAGTACAGAGTTT | 26374 |
rs215019838 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159269335 | TATAAATTATTAAAT[C/T]CTACCATCATTACAG | 26374 |
rs215046944 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159283285 | GTCCATAGCCACTAG[A/G]CTTCAAGATCTCCTC | 26374 |
rs215067417 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159316857 | GGATATCAAACATCC[C/T]CAGGCCCAAGGGCTT | 26374 |
rs215098235 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159274044 | GAGAGAGTCATACAA[A/G]GCACCTCTCCTCTTT | 26374 |
rs215110277 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159250963 | GTGTATAATATACTT[C/T]AATCATTTTTTTACC | 26374 |
rs215116195 | snp | C/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159306560 | TGACATGTGTGCTCT[C/G]CTTCCCCTTTAGTAT | 26374 |
rs215167883 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159289140 | GTCTTTGAGTCTTGG[A/G]ATTTGCAAGCTACAT | 26374 |
rs215186243 | in-del | -/A | | | intron-variant | Rfwd2 | Mm_Celera | 1:159329695 | CTAAAGAGGCATAGG[-/A]AAATATAAGACAAAA | 26374 |
rs215238692 | in-del | -/TGT | | | intron-variant | Rfwd2 | Mm_Celera | 1:159320903 | GAGCATTATTATTGA[-/TGT]TGTATGTTTCTCCAT | 26374 |
rs215271943 | in-del | -/CTAATTCATGTGACAGAAACTGCAGTGTTAGTGAGGCACC | | | intron-variant | Rfwd2 | Mm_Celera | 1:159343804 | TGTTAGCGAGGCACA[lengthTooLong]CTAATTCATGTGACG | 26374 |
rs215298652 | snp | A/C | | | intron-variant | Rfwd2 | Mm_Celera | 1:159247740 | ATTATTTCAAATTCT[A/C]TCTCTCTTGTAGATT | 26374 |
rs215299445 | snp | G/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159289993 | AGATGTACTTAATTG[G/T]TACGGTTAATTAGCC | 26374 |
rs215320128 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159250170 | TAAACGTAAAAGATA[C/T]TTTGTTTTAAATGAT | 26374 |
rs215322350 | snp | G/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159315390 | GTTTGTTTGTGTGGG[G/T]TTTTTTCTTTCTTTC | 26374 |
rs215361123 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159320512 | AATAATGTTTTTTGT[A/G]AAGCTGACACTTGTA | 26374 |
rs215393368 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rfwd2, Scarna3a, Mir1843b | Mm_Celera | 1:159339501 | GAGAATTTAAATCAG[A/G]GAAGGACGAACTCTA | 26374 |
rs215419119 | in-del | -/A | | | upstream-variant-2KB | Rfwd2 | Mm_Celera | 1:159231736 | TCAAAATCTAAACAG[-/A]AAAAAAAAATCTAAA | 26374 |
rs215420986 | in-del | -/TCTTT | | | intron-variant | Rfwd2 | Mm_Celera | 1:159310551 | TTTCTAGTTCTTTAG[-/TCTTT]TAGACTTGATGTGTC | 26374 |
rs215429055 | snp | A/C | | | intron-variant, downstream-variant-500B | Rfwd2, Scarna3a, Mir1843b | Mm_Celera | 1:159340856 | TGAAAGTGTCTATGA[A/C]GTTCTTTGTATTAAA | 26374 |
rs215433027 | in-del | -/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159286068 | TTGAGGTTAAGATGT[-/G]GTTTTTTTTTTATGG | 26374 |
rs215463365 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159331613 | CTTCTCTGAGAAGAA[A/G]GAGCCCCCATTATCA | 26374 |
rs215495247 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159265324 | TTCTGTGCTTTATTT[C/T]CTTAATAGTCACAGA | 26374 |
rs215525345 | snp | A/C | | | intron-variant | Rfwd2 | Mm_Celera | 1:159239027 | TTACTGACATCATCT[A/C]GAAGCATCATTGAAA | 26374 |
rs215554843 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159265856 | CCTCTTTCTCACCTC[A/G]TGGTCCCTACTGGTA | 26374 |
rs215554956 | snp | A/T | | | intron-variant, upstream-variant-2KB | Rfwd2 | Mm_Celera | 1:159256954 | TTGTTAATACAACTC[A/T]GGACCACTTGCACAG | 26374 |
rs215591333 | snp | A/G | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159254287 | CCGGTGCCAGAGGAA[A/G]TCAGAAGAGGGCGGT | 26374 |
rs215617102 | snp | C/T | | | upstream-variant-2KB | Rfwd2 | Mm_Celera | 1:159230206 | TGGACCTTAAAGAAG[C/T]TTTCTTCTCTATTTC | 26374 |
rs215623941 | in-del | -/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159251668 | CTTATTTTTCCTTAA[-/T]TGTTTTTTTATTTTT | 26374 |
rs215643506 | snp | A/G | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159294376 | GTGTCTCTTTATAGT[A/G]ATAAAACCCTAACTA | 26374 |
rs215730982 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159275820 | AGCAGAAACATTAGG[A/G]ATCACCATCTTACTT | 26374 |
rs215735179 | snp | C/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159343699 | AGGGAGCAATGGAGA[C/G]AAAGCGCAAGCTATG | 26374 |
rs215763971 | in-del | -/TGG | | | intron-variant | Rfwd2 | Mm_Celera | 1:159315485 | CAAAAGTCCCCCATA[-/TGG]CCCCTCCCCACTCCC | 26374 |
rs215767565 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159344041 | CAACTGGAATTATTG[A/G]CACCCTATAGTAGCT | 26374 |
rs215799374 | snp | G/T | | | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159346226 | AGCTTACATTTTTTT[G/T]AACTTAAATTATTGA | 26374 |
rs215811149 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159335980 | TCTTTCCTTTGTTCT[A/G]CTTCCCCCAAAGACT | 26374 |
rs215874956 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159261748 | GGCTGTCTCAGCTTC[C/T]GCAGTGCTGGGATTA | 26374 |
rs215875628 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159311958 | CTGGGCGTGGTGGCA[C/T]ACACCTTTAATCCCA | 26374 |
rs215879605 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159280191 | AAGACAAAATACTAG[A/G]ACCATAGAGAAGGCT | 26374 |
rs215919700 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159301778 | TACTGAAGGGCAGGA[A/G]CACACAACAAACAAA | 26374 |
rs215959255 | in-del | -/GGCAGATAGTATG | | | intron-variant | Rfwd2 | Mm_Celera | 1:159343832 | CGGTTGCCTTTACCA[-/GGCAGATAGTATG]TTTGGTAATAATGCC | 26374 |
rs215984974 | snp | A/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159241330 | TCTTAGTATTTCTTT[A/T]GTCCATATTGGAAGT | 26374 |
rs216008102 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159246400 | CCTCTTATTTGCAAA[C/T]TTTAGTATCTATATT | 26374 |
rs216033707 | snp | A/G | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159304443 | CATCCTTTCGTCTTA[A/G]CTCCAAACTTTTTCT | 26374 |
rs216040274 | snp | A/G | | | upstream-variant-2KB | Rfwd2 | GRCm38.p3 | 1:159231630 | GAGTCAGAACGTGGG[A/G]AAGTCCTCACGTTGT | 26374 |
rs216061528 | snp | G/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159295438 | CCCCATTATTGTACA[G/T]TGCTTGATGGAACCC | 26374 |
rs216077884 | in-del | -/CCCCCCCCC | | | intron-variant | Rfwd2 | Mm_Celera | 1:159342093 | TTTTCTATTCCTCCA[-/CCCCCCCCC]TTCTCTCTCCATTTA | 26374 |
rs216078046 | snp | A/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159322501 | GTGCACGAGTATGTG[A/T]GTGTGTGTGTGTGTT | 26374 |
rs216099497 | in-del | -/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159271453 | CGTGTTTGAAGAATA[-/G]AAAGAACAGATCAGT | 26374 |
rs216183972 | in-del | -/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159264738 | GTGGCTAAATTTGGC[-/T]TTTTTTCCTCCTTCC | 26374 |
rs216207562 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159232915 | TGAGCCTGGCGGGGT[C/T]CCGTGGAGGGAGGCC | 26374 |
rs216262896 | in-del | -/A | | | intron-variant | Rfwd2 | Mm_Celera | 1:159308639 | TTTTATACTTAAGAT[-/A]ATTGTGTTTGTACCA | 26374 |
rs216263847 | snp | C/T | | | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159346928 | AGCAGTTAGTGCCAC[C/T]TTGGATGCCTTTAAA | 26374 |
rs216269959 | in-del | -/A | | | intron-variant | Rfwd2 | Mm_Celera | 1:159238293 | AATGGCACAGTAGAT[-/A]AAAACAGTTGCTGTG | 26374 |
rs216310334 | snp | G/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159269676 | GGCAACAGGGCTGGG[G/T]TTTTTCTTTTGTTCT | 26374 |
rs216315991 | snp | G/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159337084 | CTCTTCATGTAGGCA[G/T]CGTAGAAGAAAGCAT | 26374 |
rs216379530 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159247476 | ACAATTCTTATTCAC[A/G]TGTTAATAACTTAAT | 26374 |
rs216391847 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159284907 | ATAACCATGAGTATA[C/T]AAGCTCCATTTAGTT | 26374 |
rs216401342 | in-del | -/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159259637 | CACACTGGTTCAGAC[-/T]TTTTTTTGGATGCTT | 26374 |
rs216402905 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159312508 | CATGGTCTAGCTTAG[C/T]GGTTAAGAGCATTTC | 26374 |
rs216409795 | snp | G/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159272041 | CAAAGCTCTGGATCT[G/T]GTCTAGGTAATAGAT | 26374 |
rs216415112 | in-del | -/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159249387 | ATGAAATAAGCAATA[-/T]TTTTTTAGTCCTTTT | 26374 |
rs216434935 | snp | A/C | | | intron-variant | Rfwd2 | Mm_Celera | 1:159300813 | TTGAAATTATAGCTC[A/C]CTGTGACTCTTGAGG | 26374 |
rs216472142 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159301675 | TGAGGAGGAAGTCTG[A/G]TATGGGCATTACATT | 26374 |
rs216475629 | in-del | -/C | | | intron-variant | Rfwd2 | Mm_Celera | 1:159325803 | GGTGATTTGGCAAGA[-/C]AAAAAAGGACAAAAA | 26374 |
rs216587556 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159323456 | TGCCCTTTTTGCTGA[C/T]ATGATTTAAAGTCTC | 26374 |
rs216589089 | snp | C/T | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159237043 | GTGTATATATATATA[C/T]ACACACACACACACA | 26374 |
rs216656974 | in-del | -/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159319693 | ACAGAAACATTTGTT[-/G]TTTTTTTTTTTTAAA | 26374 |
rs216724061 | snp | G/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159342005 | TTAGTTGTTTGAGAA[G/T]TTCATAAAATCTGTT | 26374 |
rs216738013 | in-del | -/TTTG | | | intron-variant | Rfwd2 | Mm_Celera | 1:159275241 | GTTTGCTTGTTTTGT[-/TTTG]TTTGTTTGTTTGTTT | 26374 |
rs216793367 | snp | C/T | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159333243 | AAGAATCTAAGTAGT[C/T]AAATCATCCCTGTTT | 26374 |
rs216812773 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159267633 | TTATGTCATTGTTGG[A/G]CAAACTCAGTATTTT | 26374 |
rs216835110 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159284229 | GTCCTGCCTCCACCT[C/T]CTCTGAGTCCTGAGT | 26374 |
rs216845349 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159266641 | GTTTAGTCGGCCTTT[C/T]TTGTTTTTCTTTTTT | 26374 |
rs216920345 | in-del | -/AAGGAGA | | | intron-variant | Rfwd2 | Mm_Celera | 1:159316213 | GTGGGGGGGGGGGGG[-/AAGGAGA]GAGAGAAGGAGGGCT | 26374 |
rs216927511 | snp | A/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159314788 | GCTCAGTCCACTACC[A/T]GTGGCAGCACTCCTA | 26374 |
rs216932693 | in-del | -/TT | | | intron-variant | Rfwd2 | Mm_Celera | 1:159267668 | AAGAATGCTACTCTC[-/TT]TTTTTTTTTAATTAC | 26374 |
rs216977232 | in-del | -/TCTC | | | intron-variant | Rfwd2 | Mm_Celera | 1:159236607 | GACAGACACACTCTT[-/TCTC]TCTCTGGAGATGCCT | 26374 |
rs216989545 | snp | G/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159305337 | AGTAATTAAGAAAAT[G/T]AATTTCACGCTTGCC | 26374 |
rs216997409 | in-del | -/TACT | | | intron-variant | Rfwd2 | Mm_Celera | 1:159290873 | AGTGTATAGTAGTGC[-/TACT]TGCTTCATGAATTTC | 26374 |
rs217029289 | in-del | -/ATTT | | | intron-variant | Rfwd2 | Mm_Celera | 1:159311371 | TTTCTTTTTTTAAAC[-/ATTT]ATTTATTTTATGTAT | 26374 |
rs217073145 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159344514 | AAGAAAGATGGAACT[A/G]AAATCCTGAACTGTT | 26374 |
rs217101567 | snp | A/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159344641 | GTTTAATAACTAATT[A/T]TTCATACAATGCTTT | 26374 |
rs217135185 | snp | G/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159261310 | ATATTGCTGGTCCTT[G/T]AACATGAGAGATGCT | 26374 |
rs217170431 | snp | C/T | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159286923 | GCTAAAATAAGTACC[C/T]TTTTTTGTAGGTTTG | 26374 |
rs217216365 | in-del | -/TGATAAAAAGCTGTGGC | | | intron-variant | Rfwd2 | Mm_Celera | 1:159268004 | AATCCTTGAGAGGTT[-/TGATAAAAAGCTGTGGC]TAGAACTGAATGTAA | 26374 |
rs217230060 | snp | G/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159270121 | AACTGTTGGAGTGAA[G/T]CTGAAATAAATGAGC | 26374 |
rs217248521 | snp | C/T | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159253637 | GATCCCTTTAGGAGC[C/T]GCCTAAAAGGTGATT | 26374 |
rs217258208 | snp | C/T | | | intron-variant | Rfwd2 | GRCm38.p3 | 1:159254000 | GCAGGTAATGGTCAT[C/T]TATTTATTTGCTTAA | 26374 |
rs217263446 | snp | A/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159277813 | TGCTGTTTTCCCCAG[A/T]ATTGAAAATCTTTTC | 26374 |
rs217314559 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159318824 | CTTAAGTGTCCTAAA[A/G]TTTTCTATGGTTTCA | 26374 |
rs217317658 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159320159 | TTTTTTAAGAAGCCT[A/G]TTCATTTCTCTGACT | 26374 |
rs217327153 | in-del | -/TTAAA | | | intron-variant | Rfwd2 | Mm_Celera | 1:159299383 | GTGGCACAATGTTTG[-/TTAAA]TTAAAATACATTCCT | 26374 |
rs217330002 | in-del | -/TTTTG | | | intron-variant | Rfwd2 | Mm_Celera | 1:159268505 | TTTGTTTTTTTGTTT[-/TTTTG]TTTTTTTTTGGCTTA | 26374 |
rs217357600 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159310605 | CTGCATTTCCTTTCC[C/T]CCTTCCTTTGTTCCC | 26374 |
rs217362027 | snp | A/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159235039 | TCAGTGGACAGGAGC[A/T]CTTGTTGCTCTTGCA | 26374 |
rs217389134 | snp | A/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159311344 | GACTTCATTGAGTTT[A/T]GTTCATTAATATTTC | 26374 |
rs217389708 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159234274 | TGTCCAATCAATAGT[A/G]TCACATGATAAGGTA | 26374 |
rs217389726 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159246297 | TAGTCTTTAGATTTT[C/T]CCCACTTTCTACTCC | 26374 |
rs217433632 | in-del | -/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159275985 | ATTTTAGGTGGCTGG[-/T]TTTTTTTTTTTTTTC | 26374 |
rs217451090 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159279964 | TTCTTTCTAGGGGCT[A/G]GTGTGATGGCTCAGT | 26374 |
rs217475176 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159281056 | ATCACTGTTAAGTCT[A/G]TTGTTGTATATCTTT | 26374 |
rs217476192 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159271278 | CACTAACTGCTCTTC[C/T]AGAGGTCCTGAGTTT | 26374 |
rs217500875 | in-del | -/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159275714 | TATAACTGAATTTTA[-/T]TTGTGTTTGATGCAT | 26374 |
rs217523472 | in-del | -/TTTGTGGAATCACTATTTATA | | | intron-variant | Rfwd2 | Mm_Celera | 1:159319518 | TCCTTGGTATCTATC[-/TTTGTGGAATCACTATTTATA]TCTGTGGATTTTTGA | 26374 |
rs217535927 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rfwd2 | GRCm38.p3 | 1:159257506 | ATTGCAATCTCTTTG[A/G]AGTTTGAATTTGGGC | 26374 |
rs217536518 | snp | A/C/T | | | upstream-variant-2KB | Rfwd2 | GRCm38.p3 | 1:159231892 | GCAACACCACTGCTC[A/C/T]GTACCGCCGCAGTTT | 26374 |
rs217574137 | snp | A/G | | | intron-variant | Rfwd2 | Mm_Celera | 1:159278975 | gggtttggtgtctgt[A/G]tgtgggatgggtcct | 26374 |
rs217579366 | snp | G/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159287767 | GACATAGCTCTGGGG[G/T]GTACTGGTTAGTTCA | 26374 |
rs217583306 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159271959 | AACCTGCAGCTTTAG[C/T]TTTGCAGTATTGGCC | 26374 |
rs217611731 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159278866 | GGCTACAAGCATCCC[C/T]CTCTGTATTTGCCAG | 26374 |
rs217618364 | in-del | -/TT | | | intron-variant | Rfwd2 | Mm_Celera | 1:159270766 | TATATCTGTGTGATG[-/TT]TATATCTGTGTGCAC | 26374 |
rs217664235 | in-del | -/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159236429 | GTAAACTAGTTCATA[-/T]TTTTTTTTCTTAATT | 26374 |
rs217669566 | snp | C/T | | | utr-variant-3-prime | Rfwd2 | Mm_Celera | 1:159346756 | TGCAGGAGAAACACC[C/T]ATACATATAAATAAA | 26374 |
rs217706471 | snp | G/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159322383 | AGTGTCATTGATCTG[G/T]ATATGTTGAGTCATC | 26374 |
rs217708817 | snp | A/T | | | intron-variant, upstream-variant-2KB | Rfwd2, Scarna3a, Mir1843b | Mm_Celera | 1:159339358 | AATGAAGTGCCCTAG[A/T]ACGTCAGTTTTACAC | 26374 |
rs217715989 | snp | A/C | | | intron-variant | Rfwd2 | Mm_Celera | 1:159282680 | GGCAAATGTGATGAT[A/C]TGTTTTGTTTGTTTT | 26374 |
rs217721202 | in-del | -/GGCGGGGGCGGG | | | intron-variant | Rfwd2 | Mm_Celera | 1:159328913 | GGCATCACAATGCCT[-/GGCGGGGGCGGG]GGCGGGGGCAGTGTT | 26374 |
rs217749757 | snp | C/T | | | intron-variant | Rfwd2 | Mm_Celera | 1:159273112 | GGAGATGAATGCCCA[C/T]TTGATTGTGTTTCCT | 26374 |