SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6218200 | snp | A/T | 0.5 | 0 | intron-variant | Dhx57 | Mm_Celera | 17:80278544 | ATCCTCAAACTCCTC[A/T]CAGTTTAAGGGTTCC | 106794 |
rs6223553 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Dhx57 | Mm_Celera | 17:80272908 | CCAGACCTGAGGGAG[A/G]TGGCGCTGGCCCTTA | 106794 |
rs6224199 | snp | C/T | 0.290657 | 0.246672 | synonymous-codon, nc-transcript-variant | Dhx57 | Mm_Celera | 17:80273055 | ATTCTCCACGATAAT[C/T]GATGCAGGTCCTTCA | 106794 |
rs6224791 | snp | A/C | 0.5 | 0 | intron-variant | Dhx57 | Mm_Celera | 17:80273158 | TGCCCTTTCTTTAGG[A/C]AAGGGNTAACACCAC | 106794 |
rs6224795 | snp | A/G | 0.5 | 0 | intron-variant | Dhx57 | Mm_Celera | 17:80273164 | TTCTTTAGGNAAGGG[A/G]TAACACCACTAACAA | 106794 |
rs6225223 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Dhx57 | Mm_Celera | 17:80273189 | TAACAAAGTAACAGC[A/G]CCTTGAGACAGGAAA | 106794 |
rs6225333 | snp | A/G | 0.471655 | 0.115624 | intron-variant | Dhx57 | Mm_Celera | 17:80273259 | CTGCTCTGAAACAGG[A/G]ATTTAGGATGCTAAC | 106794 |
rs6225714 | snp | C/T | 0.5 | 0 | intron-variant | Dhx57 | Mm_Celera | 17:80273283 | TGCTAACTTGAGCtt[C/T]ctccaagaaagggtc | 106794 |
rs6225747 | snp | A/G | 0.5 | 0 | intron-variant | Dhx57 | Mm_Celera | 17:80273305 | gaaagggtctctttg[A/G]gtagttttggaactt | 106794 |
rs6225856 | snp | C/T | 0.5 | 0 | intron-variant | Dhx57 | Mm_Celera | 17:80273363 | tcatagatccccctg[C/T]ctctgtcttccaagt | 106794 |
rs6242262 | snp | G/T | 0.5 | 0 | intron-variant | Dhx57 | Mm_Celera | 17:80240753 | TCTTGCTCACACAGG[G/T]AGAGTGGGCCTTTAT | 106794 |
rs6242922 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Dhx57 | Mm_Celera | 17:80240911 | GAAGAGTGTAAGCAC[A/G]CCTGACTTTAGAGAC | 106794 |
rs6242928 | snp | A/G | 0.5 | 0 | intron-variant | Dhx57 | Mm_Celera | 17:80240916 | gtgtaagcacncctg[A/G]ctttagagacttaat | 106794 |
rs6243405 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Dhx57 | Mm_Celera | 17:80241008 | GCTGGGTATATTAGG[G/T]TAAATAAAATATATT | 106794 |
rs6243927 | snp | A/G | 0.5 | 0 | intron-variant | Dhx57 | Mm_Celera | 17:80241089 | CTAATGCTTTATGCT[A/G]CATGCTCTACCTCTG | 106794 |
rs6243953 | snp | A/G | 0.5 | 0 | intron-variant | Dhx57 | Mm_Celera | 17:80241106 | ATGCTCTACCTCTGA[A/G]GTATGTtttctttct | 106794 |
rs6244026 | snp | C/T | 0.5 | 0 | intron-variant | Dhx57 | Mm_Celera | 17:80241135 | cttctttctttcttt[C/T]tttctttccttcttt | 106794 |
rs6297377 | snp | C/T | 0.5 | 0 | intron-variant | Dhx57 | Mm_Celera | 17:80244051 | ttccttgagacaggg[C/T]ctcactctncagctc | 106794 |
rs6297389 | snp | A/T | 0.5 | 0 | intron-variant | Dhx57 | Mm_Celera | 17:80244060 | acagggnctcactct[A/T]cagctctggctgtcc | 106794 |
rs6298585 | snp | G/T | 0.290657 | 0.246672 | intron-variant | Dhx57 | Mm_Celera | 17:80244265 | CCTGTCCTCATGGAT[G/T]TTATAATTCCAGGAC | 106794 |
rs6298698 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Dhx57 | Mm_Celera | 17:80244320 | ACAAATGCATACCCA[A/G]TGGCAGCAGAACAGA | 106794 |
rs6362368 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Dhx57 | Mm_Celera | 17:80259948 | GGTCCTCCGTTACTA[C/T]TTTGCCTTTGTCCTT | 106794 |
rs29497781 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dhx57 | Mm_Celera | 17:80257716 | AACAAGAAAGCCCTG[C/T]TCTTTTTGTTTTGGT | 106794 |
rs29500527 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Dhx57 | Mm_Celera | 17:80250360 | TTTTCAGGCTCTGTC[A/G]TTTGGCTCTTTCTAC | 106794 |
rs29501418 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80282071 | TGGCTCCTCAGGGTG[C/T]GGTGATCCCCCATCA | 106794 |
rs29501915 | snp | C/T | 0.32 | 0.24 | intron-variant | Dhx57 | Mm_Celera | 17:80259461 | TGTAGAATCTCAGTG[C/T]AGGTGTTCAGCGCAT | 106794 |
rs29515512 | snp | C/G | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80290651 | AATACAGTGAAGTAA[C/G]CCTGTACAAATGGAA | 106794 |
rs29517329 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Dhx57 | Mm_Celera | 17:80254901 | AATGGAAATCCCAAG[A/G]CAGCATCTGTCAGCT | 106794 |
rs29522740 | snp | A/T | 0.375 | 0.216506 | intron-variant | Dhx57 | Mm_Celera | 17:80247832 | GCTGACTTCAGACAC[A/T]CCAGAAGAGGGTGTC | 106794 |
rs29541956 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80282317 | GAACAAACACAAGAC[A/G]TTTTGTTGACAACAA | 106794 |
rs29709564 | snp | C/G | 0.165289 | 0.235211 | intron-variant | Dhx57 | Mm_Celera | 17:80272705 | AGAAAAGTCTAAGCG[C/G]TCAGGAAGGGAGTGG | 106794 |
rs29709565 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Dhx57 | Mm_Celera | 17:80272630 | CACATGCGTTTGATA[C/T]TGGCTAGCTGAGTGT | 106794 |
rs29709566 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Dhx57 | Mm_Celera | 17:80272234 | ATACATTTTTGCTGA[C/T]CTATGGGCACACAGT | 106794 |
rs29709567 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Dhx57 | Mm_Celera | 17:80271392 | GAAGTTCAATAGGAC[A/G]GAAAGCCTGTAATGC | 106794 |
rs29709568 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Dhx57 | Mm_Celera | 17:80270973 | TGAGCACTGATCTGA[C/G]CCTTGCCAATAGCAA | 106794 |
rs29709569 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Dhx57 | Mm_Celera | 17:80270337 | TAGCCACTGCTCCTG[C/T]CTTGCACGTACACGT | 106794 |
rs29709570 | snp | A/T | 0.345679 | 0.230967 | intron-variant | Dhx57 | Mm_Celera | 17:80270302 | GCTACATATCTTTTT[A/T]AAAGCAGATCTGGTT | 106794 |
rs29709571 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Dhx57 | Mm_Celera | 17:80270152 | GCCTCATGGCAGAGG[C/T]ATACATCCACAGGGT | 106794 |
rs29709572 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Dhx57 | Mm_Celera | 17:80270065 | AGCTTTCCAGCTGTC[A/G]GAACAGAATTCTCCT | 106794 |
rs29709573 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Dhx57 | Mm_Celera | 17:80269985 | GGAAAAAATGTTACT[C/T]AAGGTGTTGGTAAGA | 106794 |
rs29709814 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dhx57 | Mm_Celera | 17:80249803 | CCCCTCTGGGCAACT[A/G]CCAGCTACGCCAGCG | 106794 |
rs29709815 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80249635 | TGAAACAAAAGCTTT[A/G]TAGAGACCTTCTCCA | 106794 |
rs29709816 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80249606 | CTCCCTTTCTCCAGT[C/G]TCCAGATTGTTAGTG | 106794 |
rs29709817 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80249182 | TCCTACCTTATGGAG[G/T]CCCTGGATCACAGCT | 106794 |
rs29709818 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80249122 | TGAGCCGAGAGTAGC[A/T]AGCATTTCTCTCAGT | 106794 |
rs29709819 | snp | A/C | 0.265928 | 0.249492 | intron-variant | Dhx57 | Mm_Celera | 17:80248641 | TTTAAAGAAGGAGCT[A/C]GCAACACATCCAAGG | 106794 |
rs29709820 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Dhx57 | Mm_Celera | 17:80248337 | AATTTCTTTTGCTCG[A/G]AGTCCTTCTTTCACA | 106794 |
rs29709821 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80248173 | TCTGTGGACCGGAGA[C/T]GGAGTGTGCCACTGC | 106794 |
rs29709822 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Dhx57 | Mm_Celera | 17:80248057 | AAACATTACTACAGC[C/T]TACTGTGAACTACAG | 106794 |
rs29709823 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80247713 | ATGCATCATGGAAAG[A/G]AAGAGCCTGGTTTGT | 106794 |
rs29710494 | snp | A/T | 0.32 | 0.24 | intron-variant | Dhx57 | Mm_Celera | 17:80269886 | AAAACTAACAATGCT[A/T]AGTGTGATCCTGAGT | 106794 |
rs29710495 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Dhx57 | Mm_Celera | 17:80269870 | AGTTGAGTCTCAGTG[A/C]AAAACTAACAATGCT | 106794 |
rs29710496 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dhx57 | Mm_Celera | 17:80269700 | TCCTCTCTACACAAG[A/G]CCTTACACACCTGTA | 106794 |
rs29710497 | snp | C/G | 0.165289 | 0.235211 | intron-variant | Dhx57 | Mm_Celera | 17:80268961 | ATCTGTATGTCAAAA[C/G]AAAGGAGTCCTAAAA | 106794 |
rs29710498 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Dhx57 | Mm_Celera | 17:80268617 | TCCTTCTCGAGGGAT[C/T]TGAACCGCACGGAAA | 106794 |
rs29710499 | snp | C/G | 0.32 | 0.24 | intron-variant | Dhx57 | Mm_Celera | 17:80267817 | TCACATTAAAACTAT[C/G]AAAGAGGCCGGGTGG | 106794 |
rs29710500 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dhx57 | Mm_Celera | 17:80267729 | GACAACATTAATTCC[A/G]CTTAACAGCAATTCC | 106794 |
rs29710501 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Dhx57 | Mm_Celera | 17:80267675 | GTCACACATTAACGA[A/G]ATTTTGGAAAAGTAA | 106794 |
rs29710502 | snp | G/T | 0.197531 | 0.244432 | intron-variant | Dhx57 | Mm_Celera | 17:80267439 | AGTCTGAAACTCCAC[G/T]GGAAGCAAGCAACCA | 106794 |
rs29710503 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Dhx57 | Mm_Celera | 17:80267310 | TGGCATGATGCCCAG[C/G]AGACACTCCTGGTGA | 106794 |
rs29710694 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80247631 | GCAAGTCCTGATGCC[C/T]AGCATGATCAAAGTG | 106794 |
rs29710695 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80247568 | AGCCAGTGCTCTCGA[C/T]TGGGATGTGGTTAAG | 106794 |
rs29710696 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Dhx57 | Mm_Celera | 17:80247252 | TGCCAGCATTTGTCT[G/T]TCTTTTTTCTTTTGA | 106794 |
rs29710697 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Dhx57 | Mm_Celera | 17:80247089 | CAAAAACCAGGAGGA[C/T]TCAGGAAGTGTCCTG | 106794 |
rs29710698 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80246893 | AAGATGACTAATGAG[A/C]AATTTTTTTTCTTTT | 106794 |
rs29710699 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80246864 | GAATCCTTTCGCGCT[C/T]TGTGCAGCTACTGAA | 106794 |
rs29710700 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Dhx57 | Mm_Celera | 17:80246662 | TTAAGGACTCACACC[A/G]AATCAGTATTAAGTA | 106794 |
rs29710701 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Dhx57 | Mm_Celera | 17:80246658 | TTATTTAAGGACTCA[C/T]ACCGAATCAGTATTA | 106794 |
rs29710702 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80246550 | AGAATCCTCCTGGCT[A/G]CAACTTTGTGCACAT | 106794 |
rs29710703 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80246510 | AAATTTAGACTTGTC[A/T]GGTGAAAATTCGATC | 106794 |
rs29711384 | snp | C/G | 0.165289 | 0.235211 | intron-variant | Dhx57 | Mm_Celera | 17:80267252 | TGCTTACAGAATGAT[C/G]AAAACAACAAAAGCA | 106794 |
rs29711385 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Dhx57 | Mm_Celera | 17:80267229 | AACGCTTTAAGTTCC[C/T]GAGTGAATGCTTACA | 106794 |
rs29711386 | snp | A/T | 0.18 | 0.24 | intron-variant | Dhx57 | Mm_Celera | 17:80267220 | CTGGATGTCAACGCT[A/T]TAAGTTCCCGAGTGA | 106794 |
rs29711387 | snp | C/T | 0.396694 | 0.202437 | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80265902 | CTTAGGGTCTCTGCA[C/T]GTCAGTAACATGGCA | 106794 |
rs29711388 | snp | A/G | 0.18 | 0.24 | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80265867 | CAGGACTCCACTCTC[A/G]TTGTCCTTGAGGAAT | 106794 |
rs29711389 | snp | A/G | 0.165289 | 0.235211 | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80265802 | AGTGCTTACTGACAT[A/G]GCTCACTGCGCCCTC | 106794 |
rs29711390 | snp | C/G | 0.18 | 0.24 | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80265746 | ACTCAAATGTCATCC[C/G]AGTATGCCACTCCTC | 106794 |
rs29711391 | snp | C/T | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80265245 | GTTAAGGGTCAGACA[C/T]GTGCCACATAGGAAA | 106794 |
rs29711392 | snp | A/G | 0.165289 | 0.235211 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | Dhx57 | Mm_Celera | 17:80265203 | CAAAACTAGCAGTAA[A/G]AAGTCACTGGAGACA | 106794 |
rs29711393 | snp | A/C | 0.165289 | 0.235211 | missense, upstream-variant-2KB, nc-transcript-variant | Dhx57 | Mm_Celera | 17:80265127 | TGGAGAACAGCCCAG[A/C]GTCCAGAGTTGCACT | 106794 |
rs29711584 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80246487 | CCACAGCTGCCACAC[A/G]TTACTGCAAATTTAG | 106794 |
rs29711585 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Dhx57 | Mm_Celera | 17:80245620 | GCTTTAGGGACAGAC[C/T]GTGCTTCTCATTTGA | 106794 |
rs29711586 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80245536 | CTGTCAGTCTCTTTA[C/T]ACAGAGTCAACCTTC | 106794 |
rs29711587 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Dhx57 | Mm_Celera | 17:80245421 | TCATGACTTCCTAAA[C/G]CAACGCACAGGCGCG | 106794 |
rs29711588 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Dhx57 | Mm_Celera | 17:80245359 | CAGGCTGAAGGAAGG[A/C]CAGAATAAAGGATTG | 106794 |
rs29711589 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80245287 | CCTTTAGAATTGACA[A/G]CTACTGTGACCACAG | 106794 |
rs29711590 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dhx57 | Mm_Celera | 17:80244881 | AAGTCTTCATGACAT[C/T]AGGCTGATTCGGATG | 106794 |
rs29711591 | snp | C/G | 0.345679 | 0.230967 | intron-variant | Dhx57 | Mm_Celera | 17:80244842 | GAACTTGGTGACCAA[C/G]TGAATCAATATGGAG | 106794 |
rs29711592 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80244761 | TAGTACTTTGGGCAC[A/G]AAACAATGGAATTTG | 106794 |
rs29711593 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Dhx57 | Mm_Celera | 17:80244546 | GCATGTCTGGTGTCA[C/T]GGTAATGGAAAACCC | 106794 |
rs29712274 | snp | C/T | 0.396694 | 0.202437 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | Dhx57 | Mm_Celera | 17:80263995 | CTGATCAACAGGAAA[C/T]GCACGGCCTAGGAAA | 106794 |
rs29712275 | snp | A/G | 0.18 | 0.24 | intron-variant | Dhx57 | Mm_Celera | 17:80263727 | TACTAGCGATAGACA[A/G]ATAGTCACACTCCAT | 106794 |
rs29712276 | snp | C/G | 0.32 | 0.24 | intron-variant | Dhx57 | Mm_Celera | 17:80263702 | CTGGTCCCTGTGACC[C/G]GGGAAATGCTACTAG | 106794 |
rs29712277 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Dhx57 | Mm_Celera | 17:80263659 | TTCTTGTTACTTGAG[C/T]TAGACTATTACTCTA | 106794 |
rs29712278 | snp | C/T | 0.18 | 0.24 | intron-variant | Dhx57 | Mm_Celera | 17:80262697 | AGAGAAACCTGTTTG[C/T]ATACAATAGAAATGA | 106794 |
rs29712279 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dhx57 | Mm_Celera | 17:80262581 | AAAGAGCCTGATCTA[A/G]AAGTGACAGCTAAAA | 106794 |
rs29712280 | snp | G/T | 0.32 | 0.24 | intron-variant | Dhx57 | Mm_Celera | 17:80261694 | GCTGAGGCTTCTACA[G/T]CGAGCTGCTCCACTG | 106794 |
rs29712281 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Dhx57 | Mm_Celera | 17:80261664 | AATGCTGCCCGAGGA[A/G]CAGCGGCTGATACTG | 106794 |
rs29712282 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Dhx57 | Mm_Celera | 17:80261577 | CATCAAGGCAGCTGG[C/T]GTGCAAGCTGAGGGT | 106794 |
rs29712283 | snp | C/T | 0.32 | 0.24 | intron-variant | Dhx57 | Mm_Celera | 17:80261424 | GATGCGTGGTAAGTA[C/T]AGAGAGCCTTTTAAG | 106794 |
rs29712374 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Dhx57 | Mm_Celera | 17:80244520 | AGACTGTCATTCTGG[A/G]AACAGAAGTAGCATG | 106794 |
rs29712375 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Dhx57 | Mm_Celera | 17:80244457 | CCGCCGTCCAGGAGA[C/T]GGTTCTTAGTGGAAA | 106794 |
rs29712376 | snp | A/C | 0.32 | 0.24 | intron-variant | Dhx57 | Mm_Celera | 17:80244419 | CTTGCCAGACCAGGC[A/C]TGCACTCTACCACTA | 106794 |
rs29712377 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Dhx57 | Mm_Celera | 17:80244260 | AAGCTCCTGTCCTCA[A/T]GGATGTTATAATTCC | 106794 |
rs29712378 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Dhx57 | Mm_Celera | 17:80244157 | CTGGCTCTCTTTGTA[G/T]TCTGTCCTCGTTTTC | 106794 |
rs29712379 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80244011 | GTTTCAACCTCATGC[A/G]GCCTCTACTCTTTTT | 106794 |
rs29712380 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dhx57 | Mm_Celera | 17:80243828 | GTGTTGTCTTCCACG[C/T]GGCTAACTGAAGAGT | 106794 |
rs29712381 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dhx57 | Mm_Celera | 17:80243751 | GACCCTGTTCATTTA[C/T]ACCTACCGTCCTTTA | 106794 |
rs29712382 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Dhx57 | Mm_Celera | 17:80243686 | TCTGCGGCATTTGTT[A/C]CTGACTTATTTCCTG | 106794 |
rs29712383 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80243675 | TTAACTTTTTCTCTG[C/T]GGCATTTGTTACTGA | 106794 |
rs29713024 | snp | C/T | 0.32 | 0.24 | intron-variant | Dhx57 | Mm_Celera | 17:80261314 | ACTCACCACCAAATG[C/T]CATGGTCTCCTTTCC | 106794 |
rs29713025 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Dhx57 | Mm_Celera | 17:80261281 | TGGTGGTTCTACAAT[C/T]GTTGACTTTCTCCAG | 106794 |
rs29713026 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Dhx57 | Mm_Celera | 17:80261223 | CAGATAATTCCCATT[C/T]TAGTTCTTCTTTATG | 106794 |
rs29713027 | snp | C/G | 0.255 | 0.24995 | intron-variant | Dhx57 | Mm_Celera | 17:80260867 | CTTTTCTGAACATTG[C/G]TACAAGACCATAATC | 106794 |
rs29713028 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80260730 | ACGTTCTCAGTTGCA[A/G]TGCCCAAATCTGAAT | 106794 |
rs29713029 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Dhx57 | Mm_Celera | 17:80260698 | AATGACACGGCCTTT[C/T]AGAAGACATCTGAGC | 106794 |
rs29713030 | snp | C/T | 0.32 | 0.24 | intron-variant | Dhx57 | Mm_Celera | 17:80260557 | CTCATGTGTTACCTT[C/T]GTAGCAGACCAGGAT | 106794 |
rs29713031 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Dhx57 | Mm_Celera | 17:80260490 | CTAAAGAAGAAAGAA[A/T]TTATTCTCCCACTTT | 106794 |
rs29713032 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dhx57 | Mm_Celera | 17:80260471 | TCTCTGTGGTGCGTT[C/T]CTGCTAAAGAAGAAA | 106794 |
rs29713033 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dhx57 | Mm_Celera | 17:80259996 | CAGCTCCTAGTTCAC[C/T]TTCCTGCTCTTTCTC | 106794 |
rs29713424 | snp | A/G/T | 0.244898 | 0.249948 | intron-variant | Dhx57 | GRCm38.p3 | 17:80243334 | GCTGTTGCTGCTTCC[A/G/T]CGTCTTACAGTGTCC | 106794 |
rs29713425 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dhx57 | Mm_Celera | 17:80243263 | CTTCGTAGCTACTAC[A/G]TTATACAAACCTTGG | 106794 |
rs29713426 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Dhx57 | Mm_Celera | 17:80243111 | CATTTCAGAAAACAG[C/T]GCCCCACGTGTTCAA | 106794 |
rs29713427 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80242454 | TGGTGGTGTTCAAAA[G/T]TAGTTTTCAGAGGTG | 106794 |
rs29713428 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Dhx57 | Mm_Celera | 17:80242439 | AGTAAAAAACCCTTT[C/T]GGTGGTGTTCAAAAT | 106794 |
rs29713429 | snp | C/G | 0.32 | 0.24 | intron-variant | Dhx57 | Mm_Celera | 17:80242319 | TAACGCTTTGCAGAC[C/G]GCTCCTTCTTAGGGC | 106794 |
rs29713430 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Dhx57 | Mm_Celera | 17:80242255 | ATTAAGGACTTGCAG[A/T]TACCTTTCCTCTGGG | 106794 |
rs29713431 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Dhx57 | Mm_Celera | 17:80242167 | CCTGTAACACAAAAC[A/G]TCAGATGACAATGAG | 106794 |
rs29713432 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80241929 | ATGACCCGAGCCTTT[A/C]AGCAGATCAGCTGTC | 106794 |
rs29713433 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80241836 | CTCTGCCTCATGTTG[C/G]TTTCACGCTTCCTGC | 106794 |
rs29713994 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Dhx57 | Mm_Celera | 17:80259933 | GGTGAACACACAGCC[A/G]GTCCTCCGTTACTAC | 106794 |
rs29713995 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dhx57 | Mm_Celera | 17:80259908 | GAAGCCTGCTATGCA[C/T]GTGATCAGAGGTGAA | 106794 |
rs29713996 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80259051 | GAACTTACTCCGTTC[A/C]TTTGATGTTGATCCA | 106794 |
rs29713997 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Dhx57 | Mm_Celera | 17:80258898 | TTTAAGACTCTCCTC[A/G]ATTCTGGGCATAGTG | 106794 |
rs29713998 | snp | A/C/G | 0.260355 | 0.249785 | intron-variant | Dhx57 | Mm_Celera | 17:80258728 | ATTCACTCAAACCCC[A/C/G]AGTCGGATCATCTAG | 106794 |
rs29713999 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Dhx57 | Mm_Celera | 17:80258596 | CCTGGCCTTGACAGC[C/G]CTTTCCCTGTTAGAA | 106794 |
rs29714000 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80258551 | CCAAACGTACTTTGT[C/T]TTTCTGGAGCAGTGA | 106794 |
rs29714001 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80258265 | GTTGGGCCAGTTCAG[A/T]AGCACAGGAGTTCGC | 106794 |
rs29714002 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Dhx57 | Mm_Celera | 17:80258068 | GGCCTGAGAAGGGAG[A/T]GTTACCTGGAGGGTA | 106794 |
rs29714003 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80257961 | GGAGAAAATCACAGA[C/T]AGGATGGCCTGTAAT | 106794 |
rs29714128 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Dhx57, Morn2 | Mm_Celera | 17:80289858 | AACCTTGCTCGGAGC[C/T]GTGGGTGTGGACGAC | 106794 |
rs29714129 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Dhx57 | Mm_Celera | 17:80284530 | TGCATCTGAGGTTAC[A/G]GCTAACCTTGTTCAA | 106794 |
rs29714130 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Dhx57 | Mm_Celera | 17:80283941 | TTAAAGAATCCAACT[G/T]CTAATACTGGTAATC | 106794 |
rs29714131 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Dhx57 | Mm_Celera | 17:80283744 | GGAAGTACACAGCAC[A/G]TGGTGTCTGAGCAGA | 106794 |
rs29714132 | snp | C/G | 0.255 | 0.24995 | intron-variant | Dhx57 | Mm_Celera | 17:80283724 | GCTCACAGTTCTGAC[C/G]GCTGGGAAGTACACA | 106794 |
rs29714133 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Dhx57 | Mm_Celera | 17:80283652 | GATGGTAAGCGGGTG[G/T]ATAGTCAGTCAGGGC | 106794 |
rs29714284 | snp | C/G | 0.487535 | 0.077957 | intron-variant | Dhx57 | Mm_Celera | 17:80241783 | ACCCAGCCAGGGGTC[C/G]CTACTGCGCTGCTTC | 106794 |
rs29714285 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80241586 | TTTTTCTTCTATGAT[A/G]ATGGTAAGATCAGGG | 106794 |
rs29714286 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80241524 | CTTTACTTTTGTGGT[C/T]CTGGAGATTAAGCCC | 106794 |
rs29714287 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Dhx57 | Mm_Celera | 17:80240670 | TCATGAAACTTCTAG[C/G]CATGCGGCTTCCTCT | 106794 |
rs29714288 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Dhx57 | Mm_Celera | 17:80239599 | GTGTGTCTATGTGAA[A/G]GTGGTGTACACACTG | 106794 |
rs29714289 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Dhx57 | Mm_Celera | 17:80239557 | TGTCTATGTGAAGGT[A/G]TTGTACACACTGGTG | 106794 |
rs29714290 | snp | C/T | 0.32 | 0.24 | intron-variant | Dhx57 | Mm_Celera | 17:80239360 | TTCATACAGAAAGGC[C/T]TTTACTGATGTCTCA | 106794 |
rs29714291 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80239272 | TACAGCTTGTTAATT[C/T]TGTGTGTCTGAGTGT | 106794 |
rs29714292 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Dhx57 | Mm_Celera | 17:80239231 | TCAGAATTTTAGGGA[C/G]TGTGGCTTTTAAGCA | 106794 |
rs29714874 | snp | C/T | 0.255 | 0.24995 | intron-variant | Dhx57 | Mm_Celera | 17:80283520 | ATGGGGACCCATGCA[C/T]TGATTTATCTGTTCT | 106794 |
rs29714875 | snp | C/T | 0.408163 | 0.193609 | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80282918 | ACCTAGCTAGAAAGT[C/T]GTAGGTACCAGCACA | 106794 |
rs29714876 | snp | A/C | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80281443 | CCTGAAAGACAAAAA[A/C]ATTAATATAGACAAC | 106794 |
rs29714877 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Dhx57 | Mm_Celera | 17:80280781 | TTCTAGTTTCATTGT[C/T]ACAAGGTAGCAAAAG | 106794 |
rs29714878 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Dhx57 | Mm_Celera | 17:80280736 | TAGTATTTACTTTCC[A/T]AGAAACATTTAACTC | 106794 |
rs29714879 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Dhx57 | Mm_Celera | 17:80279742 | GTGCTGAAAAACAAA[A/G]GATCTGCATTTAACG | 106794 |
rs29714880 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Dhx57 | Mm_Celera | 17:80279705 | TACTTGAACAGGCAG[A/T]ACTCTAAGACCTATA | 106794 |
rs29714881 | snp | A/G | 0.32 | 0.24 | intron-variant | Dhx57 | Mm_Celera | 17:80279604 | GAATCTTTTATGACG[A/G]TAAGTACAGTGTTTA | 106794 |
rs29714882 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dhx57 | Mm_Celera | 17:80279299 | GCTCTAAACTAACAC[A/G]GTGAACTGCTCTTGT | 106794 |
rs29714883 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Dhx57 | Mm_Celera | 17:80279050 | CCTCCTTATTTCCTC[C/T]AGTGATTCATTCCAT | 106794 |
rs29714934 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Dhx57 | Mm_Celera | 17:80257915 | TTCAGACAGTGTCAA[A/G]TACTTGTCATGCTAT | 106794 |
rs29714935 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80257831 | CCCTGCTTCTGCTTC[C/T]ACCCAGCAAAATCCT | 106794 |
rs29714936 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Dhx57 | Mm_Celera | 17:80257420 | CATTGCTCCTAAGTA[C/T]TATGTAGTGAGCATA | 106794 |
rs29714937 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Dhx57 | Mm_Celera | 17:80257192 | GTGAGTTTTGGTAAT[C/T]TTCTAAAATTTCTTT | 106794 |
rs29714938 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Dhx57 | Mm_Celera | 17:80256937 | ACTTTATTGTTATCT[A/T]TTCCTCCCTCATGGC | 106794 |
rs29714939 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80256790 | CAAGCTGCCTGCCTT[A/G]ATACAGACTTTCATT | 106794 |
rs29714940 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80256685 | TTTATTTTTTCCACA[C/G]ACATTACCTCACTTG | 106794 |
rs29714941 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Dhx57 | Mm_Celera | 17:80256667 | GCCAAACAGCACAGG[A/G]ATTTTATTTTTTCCA | 106794 |
rs29714942 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80256633 | AAAGGAGTCGAAACC[A/G]TCACAAAAACAGAGG | 106794 |
rs29714943 | snp | A/G | 0.32 | 0.24 | intron-variant | Dhx57 | Mm_Celera | 17:80256627 | ACAAGGAAAGGAGTC[A/G]AAACCATCACAAAAA | 106794 |
rs29715744 | snp | C/T | 0.32 | 0.24 | intron-variant | Dhx57 | Mm_Celera | 17:80278785 | CTCACAACCTGAATT[C/T]GTCTTATTATGTTCC | 106794 |
rs29715745 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Dhx57 | Mm_Celera | 17:80278756 | TTTTGAAGGGCCACT[A/G]TCTTATAGAAATTCT | 106794 |
rs29715746 | snp | G/T | 0.465374 | 0.126941 | intron-variant | Dhx57 | Mm_Celera | 17:80278181 | TTTGCATTGCCAACG[G/T]GTTCTCCTCGGTATA | 106794 |
rs29715747 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Dhx57 | Mm_Celera | 17:80277888 | TATCTCTCTTGCCTC[A/C]CTTTCAGCTAACTGT | 106794 |
rs29715748 | snp | A/C | 0.21875 | 0.248039 | intron-variant | Dhx57 | Mm_Celera | 17:80277830 | CTGCTCAGGATGGTG[A/C]GAGGACACTCACTCT | 106794 |
rs29715749 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Dhx57 | Mm_Celera | 17:80277808 | CAAGATGAGCCAATC[C/T]GTGGTACTGCTCAGG | 106794 |
rs29715750 | snp | C/T | 0.32 | 0.24 | intron-variant | Dhx57 | Mm_Celera | 17:80277335 | AGACAATTAAGAAAC[C/T]ATTGCACTTGGGCAG | 106794 |
rs29715751 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Dhx57 | Mm_Celera | 17:80276583 | GCCAAAGGTGGAACT[C/T]AGGCCAACTACTCAT | 106794 |
rs29715752 | snp | C/G | 0.32 | 0.24 | intron-variant | Dhx57 | Mm_Celera | 17:80276537 | CTGACTGGCCACTCA[C/G]TAATTTCATCAAAGA | 106794 |
rs29715753 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Dhx57 | Mm_Celera | 17:80276488 | TAAGACTGAGACAAA[C/T]GACTTGTAGAGGACA | 106794 |
rs29715764 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Dhx57 | Mm_Celera | 17:80256587 | GAACTCATTACCTAC[A/C]GTCATGTCTCACTCT | 106794 |
rs29715765 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80256495 | TAACCTCTTCACTAA[C/G]GTCCCCTCAGGCTCA | 106794 |
rs29715766 | snp | A/G/T | 0.465374 | 0.126941 | intron-variant | Dhx57 | GRCm38.p3 | 17:80256291 | ATAAGAGATTATAGC[A/G/T]TGTTTCTGTCCTAAC | 106794 |
rs29715767 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80256029 | AGCATACTTCAGGAC[C/T]GGGCCATCGTTATCT | 106794 |
rs29715768 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80255992 | AAATGCCTTGCACAC[A/T]TCAGACCCAGTTAAG | 106794 |
rs29715769 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dhx57 | Mm_Celera | 17:80255244 | TCTCAAAACGGCAGC[C/T]TTTCTTTGTTAGAAT | 106794 |
rs29715770 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dhx57 | Mm_Celera | 17:80255007 | AAACAAAAACCTTGT[A/G]CCGACCTGGGAAGCG | 106794 |
rs29715771 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dhx57 | Mm_Celera | 17:80254989 | TAAAATACAGTCTTC[C/T]AGAAACAAAAACCTT | 106794 |
rs29715772 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dhx57 | Mm_Celera | 17:80254900 | CAATGGAAATCCCAA[A/G]ACAGCATCTGTCAGC | 106794 |
rs29715773 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Dhx57 | Mm_Celera | 17:80254324 | ATCAATGGTTATAGA[C/T]GTCTCAGCAATGTTG | 106794 |
rs29716384 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Dhx57 | Mm_Celera | 17:80275735 | AAAAAGCATCCCAGA[C/T]AATAATAATCCCTCC | 106794 |
rs29716385 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Dhx57 | Mm_Celera | 17:80275619 | TGCCGAGGGCAAAAC[A/G]TGACAAAGATGCTGT | 106794 |
rs29716386 | snp | C/T | 0.231111 | 0.249285 | missense, utr-variant-5-prime, nc-transcript-variant | Dhx57 | Mm_Celera | 17:80275519 | TCTGAGAAACACTGG[C/T]GGAGAAGATGCTCTA | 106794 |
rs29716387 | snp | C/T | 0.231111 | 0.249285 | missense, nc-transcript-variant | Dhx57 | Mm_Celera | 17:80274860 | AAGGTACTGGAGGGA[C/T]GTTCACAGGAGGAAC | 106794 |
rs29716388 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Dhx57 | Mm_Celera | 17:80274745 | CCCATCCTGTCCCTA[A/G]GAGCAATACTGTACG | 106794 |
rs29716389 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Dhx57 | Mm_Celera | 17:80274713 | TTACTTTTAAACTCA[C/T]TACTCTGACTGCTGA | 106794 |
rs29716390 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Dhx57 | Mm_Celera | 17:80274682 | GGAAAGAGTCCTCAT[C/T]TAGCCTCAAAGTGTT | 106794 |
rs29716391 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Dhx57 | Mm_Celera | 17:80274658 | GGATTCTGTCTGTTC[A/G]GGACCACGGGAAAGA | 106794 |
rs29716392 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80274604 | CACAGTGCTCCAGCT[G/T]CGAGTCATAGTTACA | 106794 |
rs29716393 | snp | C/T | 0.32 | 0.24 | intron-variant | Dhx57 | Mm_Celera | 17:80274550 | TGGCTGGCCACTCAC[C/T]TACACATCAGCCCAG | 106794 |
rs29716554 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80254226 | CATTAAGAGCCGTGT[A/T]ATCCTAAAAGAGGTT | 106794 |
rs29716555 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Dhx57 | Mm_Celera | 17:80254178 | GGCCATGGAACCACA[C/T]ACAATATTCCTTTAG | 106794 |
rs29716556 | snp | A/C | 0.244898 | 0.249948 | intron-variant, nc-transcript-variant | Dhx57 | Mm_Celera | 17:80252724 | TCAACTACTTACTAA[A/C]TCCCATTTTATGACA | 106794 |
rs29716557 | snp | C/T | 0.231111 | 0.249285 | intron-variant, nc-transcript-variant | Dhx57 | Mm_Celera | 17:80252567 | ACAACTAAGCCTTAC[C/T]GTAGCCTTGGTTATT | 106794 |
rs29716558 | snp | A/C/T | 0.375 | 0.216506 | intron-variant, nc-transcript-variant | Dhx57 | GRCm38.p3 | 17:80252487 | ACGCTGGCAGGAGCC[A/C/T]GAGTGGATTAGAGCA | 106794 |
rs29716559 | snp | C/T | 0.231111 | 0.249285 | intron-variant, nc-transcript-variant | Dhx57 | Mm_Celera | 17:80252391 | TTGGTGCTTGGCTTT[C/T]TCTCTTGAGGCATTT | 106794 |
rs29716560 | snp | A/G | 0.497778 | 0.0332592 | intron-variant, nc-transcript-variant | Dhx57 | Mm_Celera | 17:80252341 | GGTGTTATCAGCTCA[A/G]ATAAGACAGCTGTCT | 106794 |
rs29716561 | snp | A/G | 0.231111 | 0.249285 | intron-variant, nc-transcript-variant | Dhx57 | Mm_Celera | 17:80252112 | TATAGGTAAGGGTGT[A/G]GGAATCCAAGCCGGA | 106794 |
rs29716562 | snp | A/G | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Dhx57 | Mm_Celera | 17:80251848 | CACACAGCACAGCAT[A/G]GCTTTGAGACAAGTG | 106794 |
rs29716563 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Dhx57 | Mm_Celera | 17:80251409 | CAAGTCTCGCAACCG[C/T]ACTTTTGAGGCACGA | 106794 |
rs29717254 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dhx57 | Mm_Celera | 17:80274530 | AAGGCAGACCCTTAT[C/T]CGTCTGGCTGGCCAC | 106794 |
rs29717255 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Dhx57 | Mm_Celera | 17:80274507 | CCTCAGTCTCCACAG[C/T]CAGGAACAAGGCAGA | 106794 |
rs29717256 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Dhx57 | Mm_Celera | 17:80274293 | GGTATGAGAATCTGC[A/G]GGGCGAAACTGGACA | 106794 |
rs29717257 | snp | C/G | 0.459184 | 0.136902 | intron-variant | Dhx57 | Mm_Celera | 17:80274047 | ACTCCTACCTATGCA[C/G]TATCCTCCAGCCCCA | 106794 |
rs29717258 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Dhx57 | Mm_Celera | 17:80273993 | TGAACACCACATACT[C/G]GAAGCTGCTGCTCAG | 106794 |
rs29717384 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Dhx57 | Mm_Celera | 17:80251220 | ATTCCAATTTAGACA[A/G]ATGTCACTTACAAAA | 106794 |
rs29717385 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dhx57 | Mm_Celera | 17:80250809 | TGGGATGCTTATACA[A/G]AACCCAAACCTTTTC | 106794 |
rs29717386 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dhx57 | Mm_Celera | 17:80250337 | AGCCATCAAAGGACC[A/G]CTCTTTTTTTTCAGG | 106794 |
rs29717387 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Dhx57 | Mm_Celera | 17:80250197 | AAGCCACTACCTGGG[A/G]AAACCTCTTGCAGGG | 106794 |
rs29717388 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Dhx57 | Mm_Celera | 17:80250168 | GAGGTTTCAAATGGC[A/C]CCTTCCTATGCTGAA | 106794 |
rs29717389 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Dhx57 | Mm_Celera | 17:80250000 | TGTGGCCACACACCC[A/G]CGTTCTGAGGGCCCC | 106794 |
rs33046322 | snp | A/C/T | 0.32 | 0.24 | intron-variant | Dhx57 | GRCm38.p3 | 17:80264490 | ATCGTTTCCCCATCA[A/C/T]GCTGCTCCTTTCTCC | 106794 |
rs33048543 | snp | G/T | 0.32 | 0.24 | intron-variant, downstream-variant-500B | Dhx57 | Mm_Celera | 17:80251668 | TGTACACACAGTGCA[G/T]GTGCTCACGTCGAGG | 106794 |
rs33108484 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dhx57 | Mm_Celera | 17:80270758 | CTGTGTCACCACGCC[C/T]GGCACCTGCTCTTTC | 106794 |
rs33116004 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dhx57 | Mm_Celera | 17:80260533 | CAGAATGCTACTGTG[C/T]TGGCCCAGCTCATGT | 106794 |
rs33126283 | snp | A/G | 0.32 | 0.24 | intron-variant | Dhx57 | Mm_Celera | 17:80261864 | AGTGTATGGATCCAC[A/G]TGCTCTCTTTTAGGA | 106794 |
rs33129900 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dhx57 | Mm_Celera | 17:80238934 | CAGCTCGGCCACCTA[C/T]GATGGCAACTGCAGC | 106794 |
rs33139287 | snp | C/G | 0.444444 | 0.157135 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | Dhx57, Morn2 | Mm_Celera | 17:80290456 | ACAGCGTGGGCCCCC[C/G]AGTCTGTGGGTTCGC | 106794 |
rs33157890 | snp | A/C | 0.32 | 0.24 | intron-variant | Dhx57 | Mm_Celera | 17:80263760 | GCGCACCGGATGCAA[A/C]AGAGATGCAGAGACA | 106794 |
rs33161732 | snp | C/T | 0.444444 | 0.157135 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | Dhx57, Morn2 | Mm_Celera | 17:80290362 | CTTCCTCTCGGGAGC[C/T]GATGGACCCGGAGCC | 106794 |
rs33164085 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dhx57 | Mm_Celera | 17:80276229 | GGGACCTACATGTCA[C/T]TCAGGTCCTAGGTAA | 106794 |
rs33170089 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dhx57 | Mm_Celera | 17:80253638 | TCTCCCTCTCTCTCC[C/T]CTTCCCCTCTCCCTC | 106794 |
rs33174312 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dhx57 | Mm_Celera | 17:80244649 | TGAAGAAGGATCAAG[C/T]AGGAGTCTACAATAG | 106794 |
rs33176400 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Dhx57 | Mm_Celera | 17:80239697 | ATGTGAAGGTGGTGT[G/T]TGCCTGCATGTGTGT | 106794 |
rs33178577 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dhx57 | Mm_Celera | 17:80244675 | AATAGGACTCCATAT[A/G]TGAAGATTTAAGAAA | 106794 |
rs33178874 | snp | G/T | 0.5 | 0 | intron-variant | Dhx57 | Mm_Celera | 17:80277610 | TATGTTGCTAGGGGT[G/T]TGGGGTGGGTAGGAA | 106794 |
rs33182096 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80290916 | TGTATATATATCTAT[A/G]TATATGTATAAAGAG | 106794 |
rs33230460 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dhx57 | Mm_Celera | 17:80276491 | GACTGAGACAAATGA[C/T]TTGTAGAGGACAGAA | 106794 |
rs33234065 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Dhx57 | Mm_Celera | 17:80275740 | GCATCCCAGATAATA[A/C]TAATCCCTCCATTTT | 106794 |
rs33235672 | snp | A/G | 0.32 | 0.24 | intron-variant | Dhx57 | Mm_Celera | 17:80264590 | TCTGCTGTCACCAGG[A/G]GTGCTACCTAAATTG | 106794 |
rs33256968 | snp | A/C | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80265306 | AAGACTTAGGGAAAA[A/C]GTGTAAAACTTAGAT | 106794 |
rs33298010 | snp | C/T | 0.32 | 0.24 | intron-variant | Dhx57 | Mm_Celera | 17:80261803 | CCTCCTGGAGTCTGG[C/T]GTTACCTCTAACCCA | 106794 |
rs33303759 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Dhx57 | Mm_Celera | 17:80246606 | GAGATGGGGCACAGA[G/T]AGGACAGAGAGAACA | 106794 |
rs33322495 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dhx57 | Mm_Celera | 17:80254637 | AGAGGAAGTCTGTCA[C/T]TGTGGAGGTGGGGCT | 106794 |
rs33366443 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dhx57 | Mm_Celera | 17:80268739 | TACCCGGAAGCAAGC[A/G]GAGCTTACACACCTT | 106794 |
rs33367374 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dhx57 | Mm_Celera | 17:80238980 | CTTTCATACAAAGCA[C/T]CTGACTGGTTATCAT | 106794 |
rs33392859 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dhx57 | Mm_Celera | 17:80263178 | AATTTTAGAGATTTG[C/T]TTTTAATTAGTTGTG | 106794 |
rs33395080 | snp | A/T | 0.375 | 0.216506 | intron-variant | Dhx57 | Mm_Celera | 17:80256390 | TCCTTTAGCCTATGT[A/T]GCGTCTCCTGCCTCA | 106794 |
rs33434743 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dhx57 | Mm_Celera | 17:80247862 | CAGATCTCATTATGG[A/G]TGGTTGTGAGCCACC | 106794 |
rs33455041 | snp | C/T | 0.32 | 0.24 | intron-variant | Dhx57 | Mm_Celera | 17:80272623 | TGGTTTACACATGCG[C/T]TTGATATTGGCTAGC | 106794 |
rs33475652 | snp | C/T | 0.32 | 0.24 | intron-variant | Dhx57 | Mm_Celera | 17:80279923 | GATCCTCTCTGCCAC[C/T]CTCCAAAAACTGCAA | 106794 |
rs33478504 | snp | C/T | 0.32 | 0.24 | intron-variant | Dhx57 | Mm_Celera | 17:80247370 | CTCCCACTGCTAGAA[C/T]TAAAGATGTACTACT | 106794 |
rs33503732 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dhx57 | Mm_Celera | 17:80244659 | TCAAGCAGGAGTCTA[C/T]AATAGGACTCCATAT | 106794 |
rs33516372 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dhx57 | Mm_Celera | 17:80277951 | CAACCTGTGGGTCAC[A/G]GCCCTCACAGGGGTC | 106794 |
rs33521934 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dhx57 | Mm_Celera | 17:80279110 | GGCACAGGGCTGTAA[C/T]AGCCCAAAGAAAAAG | 106794 |
rs33546956 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Dhx57 | Mm_Celera | 17:80246776 | AAACTTAGGCAGTCT[G/T]TGTGTGTGCGCTGCA | 106794 |
rs33547843 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dhx57 | Mm_Celera | 17:80254003 | GTCTACTGTGGGACC[A/G]TGGTGTAATTACTGC | 106794 |
rs33548421 | snp | A/T | 0.375 | 0.216506 | intron-variant | Dhx57 | Mm_Celera | 17:80247821 | AGCACACTGTAGCTG[A/T]CTTCAGACACACCAG | 106794 |
rs33564431 | snp | C/T | 0.444444 | 0.157135 | downstream-variant-500B | Dhx57 | Mm_Celera | 17:80237940 | GGGATTAAAGGCGTG[C/T]GCCACCACACCCGGC | 106794 |
rs33604416 | snp | A/T | 0.32 | 0.24 | intron-variant | Dhx57 | Mm_Celera | 17:80260891 | CATAATCAAACACAC[A/T]GTAAGACTCTCACTA | 106794 |
rs33615046 | snp | A/G | 0.5 | 0 | intron-variant | Dhx57 | Mm_Celera | 17:80277698 | ACTTGCCTCCACATC[A/G]GCTCCTAGAACAGGC | 106794 |
rs33633894 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dhx57 | Mm_Celera | 17:80242367 | ACCAGAACATTTGCA[C/T]AGCATACACCAGGCC | 106794 |
rs33651131 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dhx57 | Mm_Celera | 17:80244650 | GAAGAAGGATCAAGC[A/G]GGAGTCTACAATAGG | 106794 |
rs33654957 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dhx57 | Mm_Celera | 17:80258980 | TGGGCTCATGGCCAG[C/T]TTGCTCTACACAGTG | 106794 |
rs33666424 | snp | A/G | 0.32 | 0.24 | intron-variant | Dhx57 | Mm_Celera | 17:80241357 | TTTATTTTTTATAAG[A/G]TAAGGTCTTACTATG | 106794 |
rs33667279 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dhx57 | GRCm38.p3 | 17:80240548 | TTCTTGTTTTGTTTG[C/T]TTTTTTTTAAAGTTG | 106794 |
rs33690048 | snp | A/C | 0.375 | 0.216506 | intron-variant | Dhx57 | Mm_Celera | 17:80273180 | TAACACCACTAACAA[A/C]GTAACAGCGCCTTGA | 106794 |
rs33691527 | snp | C/T | 0.32 | 0.24 | intron-variant | Dhx57 | Mm_Celera | 17:80264480 | AGTTCTAATGATCGT[C/T]TCCCCATCATGCTGC | 106794 |
rs33694619 | snp | C/T | 0.5 | 0 | intron-variant | Dhx57 | Mm_Celera | 17:80245922 | AAGGCAGGGTCTCAT[C/T]GTATAGCCAGGTTAT | 106794 |
rs33703766 | snp | A/C | 0.375 | 0.216506 | intron-variant | Dhx57 | Mm_Celera | 17:80273167 | TTTAGGCAAGGGATA[A/C]CACCACTAACAAAGT | 106794 |
rs33708048 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dhx57 | Mm_Celera | 17:80260534 | AGAATGCTACTGTGC[C/T]GGCCCAGCTCATGTG | 106794 |
rs33708669 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dhx57 | Mm_Celera | 17:80276226 | TTAGGGACCTACATG[C/T]CACTCAGGTCCTAGG | 106794 |
rs33853654 | snp | A/T | 0.375 | 0.216506 | intron-variant | Dhx57 | Mm_Celera | 17:80264136 | AAGCAGTGTCTGTGA[A/T]GCTGGAGCCTGTGTG | 106794 |
rs45835444 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80284716 | AGACTCCAAGTATTC[C/T]CTTTCCTCCAACAGG | 106794 |
rs45843201 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80283869 | TTATAATAACTATCT[C/T]GTGAGACTGGTCTCT | 106794 |
rs45874557 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80274316 | ACTGGACAGAGGCAG[C/T]GGCCTACATATATTT | 106794 |
rs45998576 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80262706 | TGTTTGCATACAATA[A/G]AAATGAACATTCCTA | 106794 |
rs46113811 | snp | G/T | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80291833 | CTTTACTAAGACCCC[G/T]AGTCCTGGAACCAGA | 106794 |
rs46183137 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80277598 | AAACCAAACATTTAT[C/G]TTGCTAGGGGTTTGG | 106794 |
rs46200787 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80240445 | ACAGGAGCTTACAGA[A/G]CTCAGCCTGCCCTCA | 106794 |
rs46302116 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80274547 | GTCTGGCTGGCCACT[C/T]ACCTACACATCAGCC | 106794 |
rs46366978 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80284747 | CACCCCTTTCTTGTG[A/G]AAGAGTGTCTGTCTT | 106794 |
rs46391639 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80283788 | CTTTGCACTGCATCT[C/G]GGCAGGGCAGGGGCG | 106794 |
rs46398755 | snp | A/G | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80292148 | CATACAAAATAAATT[A/G]AAATAGGCCATCTAG | 106794 |
rs46489886 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80274455 | ACCAAGTTAAATGAA[A/G]TCGATTTTCTGAGAA | 106794 |
rs46710362 | snp | C/T | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80291791 | GTCCCTATTTTAGTG[C/T]AGGTGACTAACTACA | 106794 |
rs47089732 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80285051 | AATAACCCCATTAAA[A/G]AATGGGGCTCAGAAC | 106794 |
rs47095330 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80278786 | TCACAACCTGAATTC[A/G]TCTTATTATGTTCCT | 106794 |
rs47226976 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80275732 | TGGAAAAAGCATCCC[A/T]GATAATAATAATCCC | 106794 |
rs47304710 | snp | A/C | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80292056 | ACTGTGAGCAGATTT[A/C]GTAATCTGATAAGCA | 106794 |
rs47337643 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80240036 | TCAGATCTCATTATG[G/T]ATGGTTGTGAGCCAC | 106794 |
rs47426061 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80261258 | CAGCTTTCTGGAAAG[C/T]TAAGACGTGGTGGTT | 106794 |
rs47551113 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80262546 | GCTATATTTCCACCC[A/T]AGGTTTAGCACTTGG | 106794 |
rs47589629 | snp | C/T | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80291832 | GCTTTACTAAGACCC[C/T]TAGTCCTGGAACCAG | 106794 |
rs47971725 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80262737 | CACAGTTCTGAAACC[A/G]TACAGGCATTGCTTT | 106794 |
rs48173732 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80278761 | AAGGGCCACTGTCTT[A/T]TAGAAATTCTCACAA | 106794 |
rs48404569 | snp | C/T | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80292156 | ATAAATTAAAATAGG[C/T]CATCTAGGGAAGATA | 106794 |
rs48450053 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80262922 | ATCAAACTCAGAATA[C/T]CAGCTTGGTGGCAAG | 106794 |
rs48621782 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80244432 | GCCTGCACTCTACCA[C/T]TAAGCTACACCGCCG | 106794 |
rs48757831 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80274456 | CCAAGTTAAATGAAG[C/T]CGATTTTCTGAGAAA | 106794 |
rs48840010 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80242325 | TTTGCAGACCGCTCC[C/T]TCTTAGGGCTGGGAA | 106794 |
rs49150111 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80243927 | TCTAGTCCTCTGAGC[C/T]CGAGGAGACCCTTCC | 106794 |
rs49246409 | snp | A/G | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80291857 | AACCAGAGGAGTTTA[A/G]GGATGAGAAGAAGTC | 106794 |
rs49528866 | snp | A/C | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80292414 | TCTTTTCATATAGGA[A/C]ATTTGTTTTATAAAA | 106794 |
rs49601657 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80240109 | GTCAGTGCTCTTAAC[C/T]GCTAAGCGGTCTCTC | 106794 |
rs49645474 | snp | A/G | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80292005 | CCAAAGAAGACGCTC[A/G]TGCCTCCGGGAGAGC | 106794 |
rs49725745 | snp | A/T | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80291325 | CACATGATACAGTGC[A/T]GCCCCCACATTTGTA | 106794 |
rs50157818 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80243926 | TTCTAGTCCTCTGAG[C/T]CCGAGGAGACCCTTC | 106794 |
rs50460729 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80277581 | AGAAAAAACAAAAAC[A/C]AAAACCAAACATTTA | 106794 |
rs50473454 | snp | C/G | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80291684 | AGGCGTTTAATGATT[C/G]TGTCTCAAGAGCCAT | 106794 |
rs50963167 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80243955 | TCCCAAGGGTTGCCA[C/T]CACTTTCCTCAGTAG | 106794 |
rs50984446 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80240037 | CAGATCTCCTTACGG[A/G]TGGTTGTGAGCCACC | 106794 |
rs51031586 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80262720 | AGAAATGAACATTCC[C/T]ACACAGTTCTGAAAC | 106794 |
rs51062352 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80274740 | CTGATCCCATCCTGT[A/C]CCTAGGAGCAATACT | 106794 |
rs51183431 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80276219 | CATTTCTTTAGGGAC[C/T]TACATGTCACTCAGG | 106794 |
rs51370875 | snp | C/T | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80292116 | AAAAAAAAAAGTTAA[C/T]TTTGTACTAATAAAA | 106794 |
rs51410002 | snp | C/T | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80292308 | AACTTACCTTTATTT[C/T]CCTCAATCTCTTAAA | 106794 |
rs51475791 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80262906 | CCATGTAGGTTTCAG[A/G]ATCAAACTCAGAATA | 106794 |
rs51501201 | snp | C/T | | | intron-variant | Dhx57 | GRCm38.p3 | 17:80286535 | GGGAAAGCTCAGAGC[C/T]TCAAACCTAGATAGA | 106794 |
rs51558238 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80274322 | CAGAGGCAGTGGCCT[A/G]CATATATTTGTATTT | 106794 |
rs51632977 | snp | A/G | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80291817 | CTACACATAAGCATT[A/G]CTTTACTAAGACCCC | 106794 |
rs51680341 | snp | G/T | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80291954 | TCCTTTTAGTCAAAA[G/T]TAAGAATGAGACATT | 106794 |
rs51688805 | snp | A/G | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80292155 | AATAAATTAAAATAG[A/G]CCATCTAGGGAAGAT | 106794 |
rs51876993 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80240052 | ATGGTTGTGAGCCAC[C/G]ATGTGGTTGCTGGGA | 106794 |
rs51951156 | snp | C/T | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80291789 | TGGTCCCTATTTTAG[C/T]GTAGGTGACTAACTA | 106794 |
rs52028495 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80283629 | CTAACTCTCTAGAGG[A/G]TCTGGTAGATGGTAA | 106794 |
rs52033850 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Dhx57 | Mm_Celera | 17:80240034 | TGTCTCACACCATCC[A/G]AAATGAGATCTGATG | 106794 |
rs52111000 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80263025 | TTTTATTGAGACAGG[A/G]TTTCTCTGTGTAGCC | 106794 |
rs52119069 | snp | C/T | | | intron-variant | Dhx57 | GRCm38.p3 | 17:80286813 | GTATATATATATACA[C/T]ATATATATATATATA | 106794 |
rs52130537 | snp | A/G | | | intron-variant | Dhx57 | GRCm38.p3 | 17:80286800 | TGTGTATATGTCTGT[A/G]TATATATATACATAT | 106794 |
rs52177868 | snp | C/T | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80291495 | ACTCTCACGAAACAA[C/T]AAACAAACAAACAAA | 106794 |
rs52320620 | snp | C/T | | | intron-variant | Dhx57 | GRCm38.p3 | 17:80286811 | CTGTATATATATATA[C/T]ATATATATATATATA | 106794 |
rs52330298 | snp | C/T | | | intron-variant | Dhx57 | GRCm38.p3 | 17:80286841 | ATATATATATATACA[C/T]ACACACACACACACA | 106794 |
rs52487328 | snp | C/T | | | intron-variant | Dhx57 | GRCm38.p3 | 17:80286839 | ATATATATATATATA[C/T]ACACACACACACACA | 106794 |
rs52507874 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80248458 | TGTTTTTTTTGTTTT[G/T]TTTTGTTTTGTTTTT | 106794 |
rs52576019 | snp | C/T | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80291487 | AGTATTACACTCTCA[C/T]GAAACAACAAACAAA | 106794 |
rs52579109 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80277579 | TCAGAAAAAACAAAA[A/C]CCAAAACCAAACATT | 106794 |
rs107595894 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80253534 | TTTTCTTTTCTTTTC[C/T]TTTTCTTTTTTCTCT | 106794 |
rs107599221 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80247050 | CACTGCTCAGCATGA[A/G]TAAATTTAAAGTTAC | 106794 |
rs107600167 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80267466 | ACCATTTTCAGCCAC[A/T]CCTTCACTTTACAGG | 106794 |
rs107608090 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80277831 | TGCTCAGGATGGTGC[A/G]AGGACACTCACTCTA | 106794 |
rs107618758 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80261012 | GTTCTAGGCCTGCCA[C/T]TAAATCACCATGCCA | 106794 |
rs107620761 | snp | C/T | | | intron-variant | Dhx57 | GRCm38.p3 | 17:80264133 | TTAAAGCAGTGTCTG[C/T]GAAGCTGGAGCCTGT | 106794 |
rs107625005 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80243477 | CACCCCAGTGAACGT[C/T]ATCCTATTGCCTTCT | 106794 |
rs107636049 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80278055 | AGCAACGAAAATAAT[A/G]TTATGGCTGGGGGGG | 106794 |
rs107640872 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80268585 | AACCAGATAAAGAGT[C/T]CTTCCGTCAGGATGC | 106794 |
rs107645526 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80265246 | TTAAGGGTCAGACAT[A/G]TGCCACATAGGAAAA | 106794 |
rs107646405 | snp | C/T | | | intron-variant | Dhx57 | GRCm38.p3 | 17:80252225 | GAGTGAGTTCCAGGA[C/T]AGCCAGGGCTATATA | 106794 |
rs107661506 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80266108 | GTATTTTACTTATTC[A/G]CTTTATTATTGGGCT | 106794 |
rs107662661 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80281610 | CATTAATATTTTACA[A/G]ATGCATGTACCTTAG | 106794 |
rs107666982 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80279013 | CATCTTAAAGCCCCA[C/G]TCTATTTGGAGACTA | 106794 |
rs107669465 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80249030 | GGTGGGCGGCTACCC[C/T]GCCATTAGGCTTGTT | 106794 |
rs107669718 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80241059 | TTTTTTGTTTTTTAA[A/T]ACCAGGGGTTGTATC | 106794 |
rs107671391 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80279399 | TCCCTCTACCTTCAA[C/T]GGTTTCCTCTCAGAG | 106794 |
rs107671465 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80253790 | GGCGTGCGCCACCAC[C/T]GCCCGGCTCTTCCTT | 106794 |
rs107673083 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80261008 | TGGAGTTCTAGGCCT[G/T]CCACTAAATCACCAT | 106794 |
rs107674130 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80257778 | GGCTGTCCTGGAACT[C/T]GATCTGTAGAAAAGC | 106794 |
rs107677795 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80241154 | CTTTCCTTCTTTCCT[C/T]CTTTCTTTCTTTCTT | 106794 |
rs107685478 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80277067 | TAAATAAATGTTGAG[A/G]AAAAAAAAAAAAAAA | 106794 |
rs107686267 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80264270 | CGTGGTTTTTCCCCC[A/G]TGTTTCTGGAGGTGT | 106794 |
rs107687987 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80264591 | CTGCTGTCACCAGGG[A/G]TGCTACCTAAATTGT | 106794 |
rs107693525 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80245384 | GGATTGGCAAATCCC[A/G]CATGCGGATGGAGGG | 106794 |
rs107694294 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80257519 | TAGGCATGGTGGTGT[G/T]CACCTTTAATCCCAG | 106794 |
rs107697282 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80246681 | CAGTATTAAGTATTA[C/G]ATGTGTGTGTGTGGT | 106794 |
rs107699635 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80246035 | ACAGTGTGTGAATGT[A/G]TATAAGTCTGTGTGT | 106794 |
rs107703343 | snp | C/T | | | downstream-variant-500B | Dhx57 | Mm_Celera | 17:80237821 | TTTTTTTTTTTTTTT[C/T]GAGACAGGGTTTCTC | 106794 |
rs107703920 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80245080 | TGACGGTGTGCCCTC[A/G]GAGGGTGGAAAAGTA | 106794 |
rs107708229 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80246008 | ATCTCCCTAGTGCTG[G/T]GATATATATTTACAG | 106794 |
rs107709893 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80276053 | AGGGAAGGGGACATT[A/T]TAAAATATTGGATGT | 106794 |
rs107715748 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80241456 | GGCCTTAGTTTCCTG[A/G]GTGGCTGGGACTACG | 106794 |
rs107715993 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80260674 | ACTATGGAAGTGCTA[C/T]CCAGGAAGAATGACA | 106794 |
rs107722225 | snp | C/G | | | intron-variant | Dhx57 | GRCm38.p3 | 17:80263516 | GCACTTTGTTTATTT[C/G]GTTTTAGTTTTATTT | 106794 |
rs107723757 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80247421 | GCTATGAACAGACAC[C/T]ATGACCAAGGCAACT | 106794 |
rs107724033 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80253954 | GTCTACTGTGGGACC[A/G]TGGTGTAATTACTGC | 106794 |
rs107726495 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80269814 | ATGGACTGAAATTAA[A/C]AAAAACTATGAGAAA | 106794 |
rs107742040 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80247530 | CAATTATTTTTTTTT[C/T]CTAGATACATTCATA | 106794 |
rs107748280 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80263085 | TAGGCTAACCTGGAA[A/C]TCAAAGATCTCCCTG | 106794 |
rs107751658 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80277150 | GGAGGCAGAGGCAGG[G/T]GGATTTCTGAGTTTG | 106794 |
rs107752813 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80282104 | ACATTACTTTGTTAG[C/T]ACTTCATAACTATAA | 106794 |
rs107758962 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80269761 | CGCACACATGTATTT[C/T]ATATTCTTCTCTTTG | 106794 |
rs107759578 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80243497 | TATTGCCTTCTTACA[C/T]ATCCTGAAACATGAC | 106794 |
rs107761038 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80239285 | TTTTGTGTGTCTGAG[G/T]GTGCATACATGTGCC | 106794 |
rs107765842 | snp | A/C | | | intron-variant | Dhx57 | GRCm38.p3 | 17:80286337 | AATAAAAAATGGAAA[A/C]AAACAAACAAACAAA | 106794 |
rs107766653 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80242293 | TTGTTATTAGATATC[A/G]AATAAGCATCTAACG | 106794 |
rs107772497 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80284899 | TGTACAACAGACCCG[A/C]CCACTGCAGAAATTC | 106794 |
rs107774134 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80260690 | CCAGGAAGAATGACA[A/C]GGCCTTTTAGAAGAC | 106794 |
rs107777436 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80246043 | TGAATGTGTATAAGT[C/G]TGTGTGTGTGTGTGT | 106794 |
rs107788113 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80281823 | GTGTTCTTACCTGTC[C/T]AGCTCCAGATTTATT | 106794 |
rs107789152 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80288035 | AGCAATGACAGATGC[A/G]AAGGTTTCAAGCTCG | 106794 |
rs107792284 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80265987 | ACTTAAAACATGTTC[A/G]GCAAGGCCTTCCTTG | 106794 |
rs107794697 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80259941 | CACAGCCGGTCCTCC[C/G]TTACTACTTTGCCTT | 106794 |
rs107795335 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80259607 | ATTTACTTAAGTATC[A/G]GGTAAATTTTACACA | 106794 |
rs107796582 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80269146 | GATCTCATTACGGAT[A/G]GTTGTGAGCCACCAT | 106794 |
rs107796770 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80279041 | CTATCCCAACCTCCT[C/T]ATTTCCTCTAGTGAT | 106794 |
rs107797759 | snp | C/G | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80292062 | AGCAGATTTCGTAAT[C/G]TGATAAGCATTGTTA | 106794 |
rs107801876 | snp | C/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | Dhx57, Morn2 | Mm_Celera | 17:80290345 | TCCATCAAGTGAGTG[C/T]GCTTCCTCTCGGGAG | 106794 |
rs107808572 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80245363 | CTGAAGGAAGGCCAG[A/G]ATAAAGGATTGGCAA | 106794 |
rs107827189 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80278849 | ATTTTACCTCCCCCC[C/T]CCGTTTTTTTTAAAG | 106794 |
rs107840622 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80270009 | GGTAAGAGGAAAAAA[A/C]CCAAGCTTTAAAAAG | 106794 |
rs107841119 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80264048 | CAGAACCCCAGTGTG[C/T]GAAGCTGGAGCCTGT | 106794 |
rs107841550 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80254009 | TGTGGGACCATGGTG[C/T]AATTACTGCTGTGAT | 106794 |
rs107841934 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80288012 | TGTGAAGAGAACATC[C/G]AAGCAGCAGCAATGA | 106794 |
rs107849425 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80243885 | AAGTCAGATGCAGTC[A/C]AGATGAGTCAGATGA | 106794 |
rs107854667 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80258969 | GCAGATTTCTGTGGG[C/G]TCATGGCCAGTTTGC | 106794 |
rs107857580 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80240248 | GGTTTTTTTTTTTTT[G/T]TTGTTGTTGTTTTTG | 106794 |
rs107860408 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80267840 | CCGGGTGGTGGTGGC[A/G]CACGCCTTTAATCCC | 106794 |
rs107863212 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80279352 | CAGGCCTTCTGAATG[C/T]ATTCCTGACTCAGCG | 106794 |
rs107867578 | snp | C/G | | | intron-variant, nc-transcript-variant | Dhx57 | Mm_Celera | 17:80253075 | GCAGAGGGGGGCCCA[C/G]TGGGACATAACCTGA | 106794 |
rs107868909 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80268375 | CATCCACATCATCCA[C/T]AACTTGAGGTCCAGG | 106794 |
rs107869998 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80250493 | GCTGCCATGTGGGTG[A/C]TGGGAATCAAACCCT | 106794 |
rs107873436 | snp | A/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80266868 | AATAAATCTTAAAAA[A/T]AAAATAAACTCTAGA | 106794 |
rs107881164 | snp | C/T | | | downstream-variant-500B | Dhx57 | Mm_Celera | 17:80237952 | GTGTGCCACCACACC[C/T]GGCAAAATAATACAT | 106794 |
rs107881705 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80247956 | ACCATCTCGCCAGCC[A/C]CATACTAATTGTTTT | 106794 |
rs107882842 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80277044 | TGCACTCACATATAT[C/T]AAATAAATAAATAAA | 106794 |
rs107888450 | snp | G/T | | | intron-variant | Dhx57 | GRCm38.p3 | 17:80286693 | ATACAGACTGAGCAG[G/T]CTATTTATGTGTTTA | 106794 |
rs107889448 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80269044 | CTGCTAACTAGAGTC[C/G]TGCTGCTCAGCCTAA | 106794 |
rs107890523 | snp | A/C | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80265505 | TTATAAGAGCTAAGC[A/C]TAACAATATCCAGTT | 106794 |
rs107896610 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80259247 | TGCTGAAGGTACGAG[C/T]GCTCACTGACATGCC | 106794 |
rs107900819 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80258481 | GAGCAAAACCAAGGC[C/T]CCCACCCAAGTCCAC | 106794 |
rs107902391 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80241353 | TCTTTTTATTTTTTA[A/T]AAGATAAGGTCTTAC | 106794 |
rs107903922 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80284398 | CACGGACCTCAGAGC[A/G]GAACTTACAGCTGCT | 106794 |
rs107905969 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80269196 | CTCAGGACCTTCGGA[A/G]GAGCAGTCAGTGCTC | 106794 |
rs107909170 | snp | A/G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80283890 | ACTGGTCTCTCTCCC[A/G/T]TGTGGTATTAATCTC | 106794 |
rs107909859 | snp | A/G | | | intron-variant, nc-transcript-variant | Dhx57 | Mm_Celera | 17:80252137 | GCCGGACCTGGTGGC[A/G]CACGCCTTTAATCTC | 106794 |
rs107911681 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80240968 | CTCAGTAGCTTTTCA[C/T]ATTGATTACACAGAA | 106794 |
rs107917604 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80277266 | CAAAAACAAAAAAAC[C/T]CCAAAAAACAAAACA | 106794 |
rs107918436 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80267826 | AACTATCAAAGAGGC[C/T]GGGTGGTGGTGGCGC | 106794 |
rs107919175 | snp | C/T | | | utr-variant-3-prime | Dhx57 | Mm_Celera | 17:80238731 | CGTGGGAGGTAGGCG[C/T]GCTCCTGTGCCTTGC | 106794 |
rs107919662 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80242845 | CTGAACACTACAGTA[A/T]TATGGGCCTCTTGTG | 106794 |
rs107923979 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80278852 | TTACCTCCCCCCTCC[G/T]TTTTTTTTAAAGACA | 106794 |
rs107925296 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80262469 | ACGCTTTGTCCACCC[G/T]CGACTAGAGACCCAT | 106794 |
rs107925732 | snp | A/G/T | | | intron-variant | Dhx57 | GRCm38.p3 | 17:80246617 | CAGATAGGACAGAGA[A/G/T]AACATTTTATTCTCA | 106794 |
rs107932010 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80247324 | CTAGACCTGGCTGGC[A/C]ATGAACTCAAAAAGA | 106794 |
rs107935298 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dhx57, Morn2 | Mm_Celera | 17:80289040 | ATCGCATTCTCCCAC[C/T]CCCCTCCCCCCACCT | 106794 |
rs107942489 | snp | A/G | | | downstream-variant-500B | Dhx57 | Mm_Celera | 17:80238133 | AGTGAGACCCCGAGG[A/G]TTGTTCTCCTCTTAG | 106794 |
rs107946315 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80247030 | GGATTAAAGGCGTGC[A/G]CCACCACTGCTCAGC | 106794 |
rs107956005 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80284035 | CAAATTTATGGTTGC[A/T]CCCTAGAGGTGGAAG | 106794 |
rs107962091 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80241228 | TTTCTCTGCGTAGCC[C/G]TGGCTATCCTGGAAC | 106794 |
rs107969821 | snp | G/T | | | intron-variant | Dhx57 | GRCm38.p3 | 17:80286934 | AGGTACAAAGGAGGG[G/T]TGGAGGGAGGAAAAG | 106794 |
rs107970422 | snp | C/T | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80292135 | GTACTAATAAAATCA[C/T]ACAAAATAAATTAAA | 106794 |
rs107972815 | snp | C/T | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80292404 | ATCTTAATTATCTTT[C/T]CATATAGGAAATTTG | 106794 |
rs107973415 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80260214 | CCATTCCTAAGTAAG[A/G]ACAGTACCTTTATAA | 106794 |
rs107974427 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80263556 | TGTAGGTACCTGTAA[A/C]GGCCAGAAGAGAGAA | 106794 |
rs107977423 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80273884 | AAAGTCAGACATGGG[C/T]TGTAGCTTAGTATAT | 106794 |
rs107979440 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80248446 | TTTGTTTTGTTTTGT[G/T]TTTTTTGTTTTGTTT | 106794 |
rs107988398 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80281912 | CTCAAGAGGCAAAGC[C/T]AGGTGGCTCTGTGAG | 106794 |
rs107994512 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80259927 | ATCAGAGGTGAACAC[A/C]CAGCCGGTCCTCCGT | 106794 |
rs107997017 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80263552 | GCCATGTAGGTACCT[A/G]TAAAGGCCAGAAGAG | 106794 |
rs108002330 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80268126 | CGAGAACACAGACAG[A/G]TCTTTCTGCTTCTGC | 106794 |
rs108016402 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80247325 | TAGACCTGGCTGGCA[A/T]TGAACTCAAAAAGAT | 106794 |
rs108018503 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80244101 | ATGTGGACCTGCCTC[C/T]GTCTCCCTAGTGCTG | 106794 |
rs108035627 | snp | C/G | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80266568 | ACTTGCTCCATAGAG[C/G]AGGCTAGCCTTGAAC | 106794 |
rs108041997 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80270568 | CCTTCAAAGCCCACG[A/G]TACAATGTGCCTGCT | 106794 |
rs108045449 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80258891 | ATGTGAATTTAAGAC[C/T]CTCCTCGATTCTGGG | 106794 |
rs108049854 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80270601 | TTCTTTTTTTTTTTT[C/T]TTTTTTCTTTTTGGT | 106794 |
rs108051611 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80253533 | TTTTTCTTTTCTTTT[C/T]TTTTTCTTTTTTCTC | 106794 |
rs108052976 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80262620 | GACAGCAAGGGTGGG[C/T]TTAACAGTAAGGAAT | 106794 |
rs108053508 | snp | A/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | Dhx57, Morn2 | Mm_Celera | 17:80290409 | CTGGGGTGGAGGGGC[A/G]CCGACAGCCCGGCGT | 106794 |
rs108053740 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80279343 | TGCATTTCCCAGGCC[G/T]TCTGAATGCATTCCT | 106794 |
rs108058138 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80243930 | AGTCCTCTGAGCCCG[A/C]GGAGACCCTTCCCAA | 106794 |
rs108061114 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80266921 | CCTCTGAAGATGTGG[C/T]TCCCGTTCTTCCCCC | 106794 |
rs108061496 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80268678 | CCCAACTGCTTGTCA[A/G]TCTCCAGATCCCCAG | 106794 |
rs108069254 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80268513 | TAACAGATACATAAA[C/T]AATAAAATACATCTA | 106794 |
rs108069861 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80273118 | TCTTTCCCCTTGAAC[A/G]GAGCGAAAGGAAACA | 106794 |
rs108070905 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80260117 | AAAGACTTTTCTTTT[A/G]TTACTATAAAAGAAG | 106794 |
rs108072089 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80279014 | ATCTTAAAGCCCCAG[G/T]CTATTTGGAGACTAT | 106794 |
rs108075668 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80271034 | TGTGTCCATAGGAAT[A/G]ATACATACATACATT | 106794 |
rs108079211 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80244342 | CAGAACAGAGGAGGC[A/G]GAGGACTCTAGAGGG | 106794 |
rs108082311 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80246970 | TCTGTAGACCAGGCT[A/G]GCCTTGAACTCAGAG | 106794 |
rs108083496 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80266486 | GGATTAAAGGTGCAC[A/G]CCACCATTCCCGGCT | 106794 |
rs108083771 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80259201 | AGCCCCAGGACCCCC[A/T]GTTTGTTGTGTCTGT | 106794 |
rs108086430 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80288011 | TTGTGAAGAGAACAT[C/T]CAAGCAGCAGCAATG | 106794 |
rs108092485 | snp | G/T | | | intron-variant, upstream-variant-2KB | Dhx57 | GRCm38.p3 | 17:80281673 | TTTATTTTTTTAATA[G/T]TTATTTATTTATTTA | 106794 |
rs108092490 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80248975 | TGTCCAGGCTGGCCT[C/T]GAACTCAGAGATCCG | 106794 |
rs108094136 | snp | A/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | Dhx57, Morn2 | Mm_Celera | 17:80290432 | CCCGGCGTCGGGGGA[A/T]CCGGAGATACAGCGT | 106794 |
rs108104309 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80257927 | CAAGTACTTGTCATG[C/T]TATGCAGAGTAAATG | 106794 |
rs108108466 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80276495 | GAGACAAATGACTTG[G/T]AGAGGACAGAAGAAT | 106794 |
rs108109777 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80277289 | ACAAAACAAAACAAA[A/T]CAAAAACCCCACAGT | 106794 |
rs108111607 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80278640 | TCTTTGTGTAGCCCT[G/T]GTGTCCCTCCATGGA | 106794 |
rs108116211 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80264165 | TGTGTGTGTGTGTGT[C/G]TGTGTGTGTGTGTGT | 106794 |
rs108117661 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80256373 | CTTGGTAGTTCAGGC[G/T]GTCCTTTAGCCTATG | 106794 |
rs108126060 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80264203 | TGTGTGTGTCTGTGT[C/G]TGTGTCTGTGTGCTC | 106794 |
rs108126873 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80254496 | TTGAGACTGACCGAC[C/T]TTGCTGGGTACAGTT | 106794 |
rs108132277 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80273170 | AGGCAAGGGATAACA[C/T]CACTAACAAAGTAAC | 106794 |
rs108139013 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80259445 | TAATACAACACAATG[C/T]TGTAGAATCTCAGTG | 106794 |
rs108140732 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80287943 | CTGAATGCCTCACTC[A/G]ATAACCTATGAGTGG | 106794 |
rs108146973 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80254833 | TGTAAGCTAGCCCTA[A/G]TCAACTCTTGTCCCT | 106794 |
rs108164145 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80239284 | ATTTTGTGTGTCTGA[A/G]TGTGCATACATGTGC | 106794 |
rs108167117 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80239222 | TTCCAGGTCTCAGAA[C/T]TTTAGGGACTGTGGC | 106794 |
rs108167338 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80264169 | TGTGTGTGTGTCTGT[G/T]TGTGTGTGTGTGTGT | 106794 |
rs108176320 | snp | A/C | | | intron-variant | Dhx57 | GRCm38.p3 | 17:80286366 | AACAAACAAAAAAAA[A/C]CAAAGGGATTGTGAG | 106794 |
rs108177926 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80257092 | ACTGCCTGTTGCTAT[A/G]TCCACCAGGGTGGCC | 106794 |
rs108179020 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80268675 | AGCCCCAACTGCTTG[C/T]CAATCTCCAGATCCC | 106794 |
rs108180391 | snp | A/C | | | intron-variant, upstream-variant-2KB | Dhx57, Morn2 | Mm_Celera | 17:80288935 | CGAGCTCTCCAAAGG[A/C]CAGCAGTATATACAT | 106794 |
rs108183039 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80284945 | GCTGAGAACAGAGAT[G/T]GTGTGGTGTCTAGTC | 106794 |
rs108185165 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80254794 | GCTTCCTACCATGAC[A/G]ATAATTGACTGAACC | 106794 |
rs108186622 | snp | A/G | | | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | Dhx57 | Mm_Celera | 17:80281285 | ACTGCCGCCGCCTCC[A/G]CCGCCGCAGCTACCG | 106794 |
rs108187415 | snp | A/C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80270743 | GCTGGGATTAAAGGC[A/C/G]TGTGTCACCACGCCC | 106794 |
rs108194086 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80261195 | TTGTTTTTGCCCTCC[C/T]ACCTTGCTCTCCCAG | 106794 |
rs108197874 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80247957 | CCATCTCGCCAGCCC[A/C]ATACTAATTGTTTTA | 106794 |
rs108201644 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80243421 | CCTGACCCTGTCCCA[C/T]TTGTCGCTGCACAGC | 106794 |
rs108206167 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80250424 | TGGTGTTTTGCCTGC[A/G]GGTGTCAGTAAGGGT | 106794 |
rs108209807 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80284725 | GTATTCCCTTTCCTC[C/T]AACAGGCACCCCTTT | 106794 |
rs108222352 | snp | A/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | Dhx57, Morn2 | Mm_Celera | 17:80290402 | ATCCACTCTGGGGTG[A/G]AGGGGCACCGACAGC | 106794 |
rs108223642 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80246000 | CCTGTTTCATCTCCC[C/T]AGTGCTGGGATATAT | 106794 |
rs108227100 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80269275 | GAGTCCCCAGGCCTC[A/G]TAAATCCTAGGAACA | 106794 |
rs108227516 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80240823 | TGGCTTATGACAGCC[A/T]GACAGCCACTGGTCA | 106794 |
rs108231328 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80268094 | GTCCTAGAGCTCGCC[A/C]TATAGAACAGGCTGG | 106794 |
rs108232794 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80273122 | TCCCCTTGAACGGAG[C/T]GAAAGGAAACAGCTT | 106794 |
rs108233076 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80246932 | AGGGTTTCTCTGTGT[A/C]CCCGGGCTGTCCCGG | 106794 |
rs108235573 | snp | A/C | | | intron-variant | Dhx57 | GRCm38.p3 | 17:80287096 | TTATGAAATTCCTAG[A/C]CAAATGGATGGACCT | 106794 |
rs108237310 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80266062 | TCTTGCCATGCACTT[C/T]TTATCTTTTCTTCTT | 106794 |
rs108239931 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80265462 | GGTATACAAAAGGCA[C/T]GTACAAAGATTTTCA | 106794 |
rs108243443 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80276624 | AAAAATAAATGAACC[C/T]CTTCAACTGATAGTG | 106794 |
rs108252148 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80266012 | TCCTTGGCTAACCTT[A/G]GCTAACCTATTTAAG | 106794 |
rs108254198 | snp | G/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80281638 | TAGGACTAATATGTA[G/T]TAAGTTTCTCTGACA | 106794 |
rs108257867 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80268648 | GTGGCTATTAATAAA[C/T]CGCAGGCACATAGCC | 106794 |
rs108259517 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80248444 | TTTTTGTTTTGTTTT[G/T]TTTTTTTTGTTTTGT | 106794 |
rs108267403 | snp | A/C | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80266379 | TTCAAGACAGGGTTT[A/C]TCTGTGTAACCCTGG | 106794 |
rs108268851 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80243301 | CCGGGACCACTGCAG[A/G]GCTTGCTCTGTGCTC | 106794 |
rs108275612 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80260216 | ATTCCTAAGTAAGGA[C/T]AGTACCTTTATAACG | 106794 |
rs108282529 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80242629 | ACAGTTTGACATCAA[A/G]CTCGTATATCTGCTG | 106794 |
rs108286238 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80264098 | TGTGTGTGTTTGTGT[C/G]TGTGTGCTGCAAGTA | 106794 |
rs108286332 | snp | A/C | | | intron-variant | Dhx57 | GRCm38.p3 | 17:80286357 | AAACAAACAAACAAA[A/C]AAAAAAAACCAAAGG | 106794 |
rs108302256 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80240824 | GGCTTATGACAGCCT[C/G]ACAGCCACTGGTCAT | 106794 |
rs108308588 | snp | A/G | | | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | Dhx57 | Mm_Celera | 17:80265140 | AGCGTCCAGAGTTGC[A/G]CTCATGAGAATGACC | 106794 |
rs108312454 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80241221 | GACAGGGTTTCTCTG[C/T]GTAGCCCTGGCTATC | 106794 |
rs108318552 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80253361 | GACACTATCTCTCTC[C/T]ACCCCCTCCATTAGT | 106794 |
rs108326223 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dhx57, Morn2 | Mm_Celera | 17:80288427 | AAGTAAAGCTTTCAA[C/T]AAATGTTTTGGTAAC | 106794 |
rs108336310 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80264107 | TTGTGTCTGTGTGCT[C/G]CAAGTACACATTAAA | 106794 |
rs108342491 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80257493 | AACCCTTCAACAAAA[A/T]TTTTTTTAGTTAGGC | 106794 |
rs108352668 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80241290 | AGAAATCTGCCTGCC[C/T]CTGCCTCCCAAGTGC | 106794 |
rs108356506 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80246989 | TTGAACTCAGAGATC[C/T]GCCTGCCTCTGCCTC | 106794 |
rs108359518 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80243929 | TAGTCCTCTGAGCCC[A/G]AGGAGACCCTTCCCA | 106794 |
rs108362433 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80268345 | GTTCCTAGCACTTAC[A/G]AGGTGGCTTACAGCC | 106794 |
rs108365021 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80257609 | ATGAGTTCTAGGTTA[C/T]CTAGAACCTCAAAGT | 106794 |
rs108365057 | snp | C/G/T | | | intron-variant | Dhx57 | GRCm38.p3 | 17:80261695 | CTGAGGCTTCTACAG[C/G/T]GAGCTGCTCCACTGC | 106794 |
rs108365078 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80247413 | GTTCTACTGCTATGA[A/G]CAGACACCATGACCA | 106794 |
rs108370238 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80276618 | AAACATAAAAATAAA[C/T]GAACCCCTTCAACTG | 106794 |
rs108382089 | snp | C/G | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80291844 | CCCCTAGTCCTGGAA[C/G]CAGAGGAGTTTAAGG | 106794 |
rs108384529 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80276868 | TTAAAAAAAAAAAAA[A/T]AAGACACAGTGCAGA | 106794 |
rs108389141 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80263548 | TTTAGCCATGTAGGT[A/G]CCTGTAAAGGCCAGA | 106794 |
rs108390337 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80281580 | GGCTAAATTGCTTCA[C/T]ATAATCATTATTATC | 106794 |
rs108393849 | snp | C/T | | | intron-variant | Dhx57 | GRCm38.p3 | 17:80252195 | TTTCTGAGTTCAAGG[C/T]CAGCCTGGTCTACAG | 106794 |
rs108395140 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80244597 | TGCAGCACACAGAGA[C/G]ACAGAGGAAGTGAGT | 106794 |
rs108398322 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80264887 | GACGTTAAGGTCACA[C/T]ACAAACTTAACATCT | 106794 |
rs108401228 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80267364 | GTGCTTCCAACCTTC[A/G]AGATCAAGAAAGCCA | 106794 |
rs108401279 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80268441 | CATGCACCTGATGCA[A/G]CAGACATACATGCAG | 106794 |
rs108403251 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80241032 | ATATATTAGGGTTTT[G/T]TTTTGTTTTGTTTTT | 106794 |
rs108413296 | snp | G/T | | | intron-variant, upstream-variant-2KB | Dhx57, Morn2 | Mm_Celera | 17:80288482 | GACTTCAGTATTAGC[G/T]GCATTGTGAGTGGTA | 106794 |
rs108413890 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80267042 | TAGATGGGATTCCCT[C/T]GCGTATTTCACTTAT | 106794 |
rs108416796 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80257001 | CAAATATATCACTGA[G/T]TCTTTTGTTGTTGTT | 106794 |
rs108418994 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80269608 | GCTGGCCTCTAGCTT[C/T]GTGCCAGGCTCAGTT | 106794 |
rs108419158 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80261662 | AGAATGCTGCCCGAG[A/G]AGCAGCGGCTGATAC | 106794 |
rs108420140 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80264145 | CTGTGAAGCTGGAGC[C/T]TGTGTGTGTGTGTGT | 106794 |
rs108425893 | snp | C/T | | | intron-variant | Dhx57 | GRCm38.p3 | 17:80286465 | GAAGGCTCATCAATA[C/T]GTTTGCCTAGGTAAG | 106794 |
rs108429685 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80242269 | GATACCTTTCCTCTG[A/G]GCTTGCTGTTGTTAT | 106794 |
rs108432238 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80262974 | CTAGCCTCCTCTTTT[A/T]AAAAAAAAATCTTTA | 106794 |
rs108440551 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80242846 | TGAACACTACAGTAT[A/T]ATGGGCCTCTTGTGA | 106794 |
rs108442399 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80268346 | TTCCTAGCACTTACG[A/T]GGTGGCTTACAGCCA | 106794 |
rs108442554 | snp | A/C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80284381 | GAGTTCCTCACGGAC[A/C/G]TCACGGACCTCAGAG | 106794 |
rs108444121 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80273885 | AAGTCAGACATGGGC[G/T]GTAGCTTAGTATATC | 106794 |
rs108446574 | snp | A/C | | | intron-variant | Dhx57 | GRCm38.p3 | 17:80287806 | GGTGGGTATGGGGGA[A/C]TTTTGGTATAGCATT | 106794 |
rs108447760 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80270035 | AAAAGAGAAGGGTAA[A/G]CATAAAAGATATGCA | 106794 |
rs108451574 | snp | A/G | | | downstream-variant-500B | Dhx57 | Mm_Celera | 17:80237877 | TCACTTTGTAGACCA[A/G]GCTGGCCTCGAACTC | 106794 |
rs108454378 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80246065 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 106794 |
rs108465084 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80246615 | CACAGATAGGACAGA[G/T]AGAACATTTTATTCT | 106794 |
rs108468171 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80243884 | TAAGTCAGATGCAGT[C/T]AAGATGAGTCAGATG | 106794 |
rs108469823 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80241466 | TCCTGGGTGGCTGGG[A/G]CTACGGGTATATATA | 106794 |
rs108472594 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80245604 | GGACTAAGGCTTGTC[C/T]GCTTTAGGGACAGAC | 106794 |
rs108473837 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80242916 | TTTTCTAGATTTATT[C/T]ATTTTATGTGTGTTT | 106794 |
rs108482439 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80265812 | GACATGGCTCACTGC[A/G]CCCTCACTTCCTTCT | 106794 |
rs108482689 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80268431 | AAACAGCAGGCATGC[A/G]CCTGATGCAACAGAC | 106794 |
rs108485309 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80242635 | TGACATCAAACTCGT[A/G]TATCTGCTGAGCCAT | 106794 |
rs108489517 | snp | A/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80282053 | AGCTGCAACACTTTC[A/T]TTTGGCTCCTCAGGG | 106794 |
rs108495126 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80267491 | TACAGGCGTGTGTGC[C/T]CACTGGGAACACCTT | 106794 |
rs108499800 | snp | A/G | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80291711 | CCATTCATTCCCTAG[A/G]TAAGCATTTTCTGTT | 106794 |
rs108503989 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80282294 | CACAGAGAAAACTAG[A/G]GACAGAGGAACAAAC | 106794 |
rs108504371 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80248208 | TGGCTCCCACCCACC[C/T]CACATCTCAGTGTCA | 106794 |
rs108505571 | snp | C/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | Dhx57, Morn2 | Mm_Celera | 17:80290455 | TACAGCGTGGGCCCC[C/G]GAGTCTGTGGGTTCG | 106794 |
rs108513992 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dhx57, Morn2 | Mm_Celera | 17:80288272 | GTCAGGGAGACTTTG[A/G]GATAGAATGCTAGCT | 106794 |
rs108514210 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80267486 | CACTTTACAGGCGTG[C/T]GTGCCCACTGGGAAC | 106794 |
rs108519291 | snp | C/T | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80291739 | GTTTGTACTCAATAC[C/T]GAGTCAGGTGGTGGG | 106794 |
rs108519876 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80247018 | TCCAAAGTGCTGGGA[A/T]TAAAGGCGTGCACCA | 106794 |
rs108523504 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80265833 | ACTTCCTTCTGCGCT[C/T]TCCCAACCAGGCAGG | 106794 |
rs108524281 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80263784 | AGAGACACTAACCAC[A/G]GTTCAGAGTTAGTAA | 106794 |
rs108525909 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80258890 | CATGTGAATTTAAGA[A/C]TCTCCTCGATTCTGG | 106794 |
rs108526775 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80276443 | CCATCTCTTAGTCAG[A/G]GATACTACCCCTGTC | 106794 |
rs108531946 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80281575 | AGAATGGCTAAATTG[C/T]TTCACATAATCATTA | 106794 |
rs108532493 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80265791 | CTTCTCGTTAGAGTG[C/T]TTACTGACATGGCTC | 106794 |
rs108533474 | snp | A/C | | | downstream-variant-500B | Dhx57 | Mm_Celera | 17:80237854 | TGTAGCCCTGGCTGT[A/C]CTGGACCTCACTTTG | 106794 |
rs108534370 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80270038 | AGAGAAGGGTAAGCA[C/T]AAAAGATATGCAGCT | 106794 |
rs108536508 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80276392 | AAGGTGCTTATCCTA[G/T]CCTAAGTCCAGAGCC | 106794 |
rs108550361 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80248036 | AAAGGCTGGCCTGTT[G/T]TGAGGAAACATTACT | 106794 |
rs108552213 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80257208 | TTCTAAAATTTCTTT[C/T]TGGCTGGAATGTTTG | 106794 |
rs108563815 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80263786 | AGACACTAACCACAG[C/T]TCAGAGTTAGTAAGT | 106794 |
rs108566262 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80266965 | CTTCCATTAACTACT[A/G]CCTGCCACACTGGCT | 106794 |
rs108569117 | snp | C/T | | | intron-variant, nc-transcript-variant | Dhx57 | Mm_Celera | 17:80252151 | CACACGCCTTTAATC[C/T]CAGCACTCGGGAGGC | 106794 |
rs108571006 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80266375 | GTTTTTCAAGACAGG[A/G]TTTCTCTGTGTAACC | 106794 |
rs108572049 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80241289 | CAGAAATCTGCCTGC[C/G]TCTGCCTCCCAAGTG | 106794 |
rs108579144 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80262440 | CTGTGTGCGTCTGTC[C/T]GTCAATCCATCGTAC | 106794 |
rs108582222 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80284910 | CCCGACCACTGCAGA[A/G]ATTCACAACTGATCA | 106794 |
rs108584682 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80284965 | GGTGTCTAGTCCCAA[A/C]TGACTCACCCACAAA | 106794 |
rs108592485 | snp | A/C | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80265225 | CTGGAGACAAGAAAA[A/C]GATAGTTAAGGGTCA | 106794 |
rs108598923 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80258485 | AAAACCAAGGCTCCC[A/C]CCCAAGTCCACACAC | 106794 |
rs108605622 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Dhx57, Morn2 | Mm_Celera | 17:80289789 | TTCCCCAAACAGCCC[C/T]TCGGGTCGCCACCGA | 106794 |
rs108607690 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80287981 | AATAGGTGGAGAAAG[C/T]GAGCCATGAAATACT | 106794 |
rs108608661 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80265661 | AACAGACTAACAGTA[C/T]ACCAGCAACATTCTT | 106794 |
rs108613073 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80276446 | TCTCTTAGTCAGAGA[C/T]ACTACCCCTGTCCCT | 106794 |
rs108614657 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80249742 | TCATCTTCAGAAATC[C/T]ATTTTGCATAGCTGA | 106794 |
rs108619040 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80277412 | AGTGGTTAAAAGCAC[C/T]GGCTGCTTTTTCAGA | 106794 |
rs108628626 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80261397 | TAGCAGTGTGGTGGG[A/G]TATGGTGCGGTGATG | 106794 |
rs108631902 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80243561 | TTCCTGTGCTGGAAT[A/G]TTCTCTCCTTAGAGA | 106794 |
rs108635529 | snp | G/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80282349 | TAGAACGTGATGATG[G/T]GCATAACTCCCACTA | 106794 |
rs108638963 | snp | A/G | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80291593 | CTATGCTCATCAAAC[A/G]TGGAAATCTGAAGAG | 106794 |
rs108641700 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80266029 | CTAACCTATTTAAGA[C/T]TTCACATGCACCCCA | 106794 |
rs108644779 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80248459 | GTTTTTTTTGTTTTG[G/T]TTTGTTTTGTTTTTT | 106794 |
rs108645129 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80277031 | AAGACAGCAACAGTG[C/T]ACTCACATATATTAA | 106794 |
rs108648852 | snp | G/T | | | intron-variant, upstream-variant-2KB | Dhx57, Morn2 | GRCm38.p3 | 17:80288410 | TGTGTGTGTGTGTGT[G/T]TAAGTAAAGCTTTCA | 106794 |
rs108650611 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80261880 | TGCTCTCTTTTAGGA[C/T]TATCCTATTATAAGT | 106794 |
rs108651051 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80248463 | TTTTTGTTTTGTTTT[G/T]TTTTGTTTTTTCGAG | 106794 |
rs108651945 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80257793 | CGATCTGTAGAAAAG[C/T]CTGGCCTCAAACTCA | 106794 |
rs108652987 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80247056 | TCAGCATGAATAAAT[A/T]TAAAGTTACTAACAG | 106794 |
rs108665195 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80259160 | CTGAGCCTGAAGCCC[A/G]TTTTCAATTCGACTG | 106794 |
rs108669384 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80269074 | ACACCTTTTTTTTTT[A/T]AATTATTATATATAA | 106794 |
rs108672075 | snp | A/C | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80266273 | TTCCATAAGAAAAAA[A/C]CACCTGAAAATAAAA | 106794 |
rs108672436 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80247493 | GGTGGGAGCATGGCA[A/G]CAGCCAGTCTTAAAG | 106794 |
rs108686309 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80269175 | ATGTGGTTGCTGGGA[A/T]TTGAACTCAGGACCT | 106794 |
rs108695198 | snp | A/C | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80291513 | ACAAACAAACAAAAC[A/C]AAAAAAAAAAAAACC | 106794 |
rs108699577 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80271401 | TAGGACGGAAAGCCT[A/G]TAATGCTCTATAGCA | 106794 |
rs108707657 | snp | A/C | | | downstream-variant-500B | Dhx57 | Mm_Celera | 17:80237860 | CCTGGCTGTCCTGGA[A/C]CTCACTTTGTAGACC | 106794 |
rs108708885 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80259840 | TTTGAATTGTGTTGT[C/T]AAGGACGCACTCCTC | 106794 |
rs108709508 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80284092 | GCAGTGCAGACACAG[A/G]GCCCAGCGGACCTGA | 106794 |
rs108711886 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80260116 | CAAAGACTTTTCTTT[A/T]GTTACTATAAAAGAA | 106794 |
rs108712146 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80277264 | AACAAAAACAAAAAA[A/C]CCCCAAAAAACAAAA | 106794 |
rs108717318 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80264478 | TAAGTTCTAATGATC[A/G]TTTCCCCATCATGCT | 106794 |
rs108717584 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80271033 | ATGTGTCCATAGGAA[C/T]GATACATACATACAT | 106794 |
rs108720739 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80262894 | AGTTTTCTCCTTCCA[C/T]GTAGGTTTCAGGATC | 106794 |
rs108721204 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80248207 | CTGGCTCCCACCCAC[A/C]CCACATCTCAGTGTC | 106794 |
rs108725260 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80241620 | ATCACTAAGGAGGGC[C/T]AACACCCTCTCTTTG | 106794 |
rs108731533 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80256278 | AAAATAAGCAACAAT[A/T]AGAGATTATAGCATG | 106794 |
rs108733074 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80268064 | TTTGGAGACAGGGTA[C/G]ATATAGTCTTGAGTG | 106794 |
rs108733199 | snp | A/G | | | downstream-variant-500B | Dhx57 | Mm_Celera | 17:80237992 | AGGTGTCTGGTGTGT[A/G]GGGAGGCTGTGACCC | 106794 |
rs108734948 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80258441 | TCATGCACAAGGCGG[C/T]ACATCTAGTTTCTAT | 106794 |
rs108735715 | snp | G/T | | | intron-variant, nc-transcript-variant | Dhx57 | Mm_Celera | 17:80252491 | TGGCAGGAGCCAGAG[G/T]GGATTAGAGCACGGG | 106794 |
rs108736301 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80267999 | AAGACTCTCTCTCTC[A/T]CACACACACATACAT | 106794 |
rs108736347 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80282257 | TAGGAAATAGTTAAT[A/G]GTCAATTCACAAAGA | 106794 |
rs108736994 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80254575 | GCTTGGCCCATGGGA[A/C]GTGGCACTATTAGGG | 106794 |
rs108739546 | snp | A/G | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80292001 | CTACCCAAAGAAGAC[A/G]CTCGTGCCTCCGGGA | 106794 |
rs108739825 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80257614 | TTCTAGGTTACCTAG[A/C]ACCTCAAAGTGAGAC | 106794 |
rs108740240 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80262799 | ATGTGTGTGCGTGCA[C/T]GCAAGTGTACACTCG | 106794 |
rs108741553 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80268623 | TCGAGGGATTTGAAC[C/T]GCACGGAAAGTGGCT | 106794 |
rs108741648 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dhx57, Morn2 | Mm_Celera | 17:80289495 | AATACAAATTAGGTT[A/G]TCTAGTCCGCAGGGA | 106794 |
rs108752025 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80273551 | TAATGAAATATCCCT[C/T]AACAACAAAAAGGAA | 106794 |
rs108758555 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80269534 | ACATGAGTGTGCAAG[A/C]CCCTGTAACCCCAGT | 106794 |
rs108760324 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80256138 | AAAAACAAAACAAAA[C/T]GAAACAGAAACTATA | 106794 |
rs108762335 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80266593 | TTGAACTCCATCTGT[C/T]CTGCTTGAGTGCTGG | 106794 |
rs108763321 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80271472 | GTGTCACATGGTAAG[C/T]TCTGGCCAGGTGGGC | 106794 |
rs108766332 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80269651 | GGCATTGAGGCAGAG[A/T]GTGACAGAGCAGGAC | 106794 |
rs108784557 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80241352 | TTCTTTTTATTTTTT[A/T]TAAGATAAGGTCTTA | 106794 |
rs108784778 | snp | A/C | | | intron-variant, upstream-variant-2KB | Dhx57, Morn2 | Mm_Celera | 17:80288531 | AGATTTGAATCCAAG[A/C]CTGGTTAGTTTTTAT | 106794 |
rs108794322 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80262973 | TCTAGCCTCCTCTTT[A/T]TAAAAAAAAATCTTT | 106794 |
rs108799421 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dhx57, Morn2 | Mm_Celera | 17:80289027 | TGAATTTTCAATAAT[C/T]GCATTCTCCCACCCC | 106794 |
rs108800330 | snp | A/G | | | intron-variant | Dhx57 | GRCm38.p3 | 17:80286714 | TATGTGTTTAGGAGT[A/G]TATATATATATATAT | 106794 |
rs108804767 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80257216 | TTTCTTTCTGGCTGG[A/C]ATGTTTGTTTTAAAA | 106794 |
rs108806462 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80272492 | TGTAAGCCTTTGAGA[C/T]GGCATATGAGTTTCC | 106794 |
rs108808399 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80242777 | CCTCTGCCTCCCAAG[C/T]GCTGGGATTAAAGGC | 106794 |
rs108813227 | snp | C/T | | | downstream-variant-500B | Dhx57 | Mm_Celera | 17:80237820 | TTTTTTTTTTTTTTT[C/T]CGAGACAGGGTTTCT | 106794 |
rs108816271 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80253960 | TGTGGGACCGTGGTG[C/T]AATTACTGCTGTGAT | 106794 |
rs108817100 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80254493 | CCTTTGAGACTGACC[A/G]ACCTTGCTGGGTACA | 106794 |
rs108818460 | snp | A/G | | | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | Dhx57 | Mm_Celera | 17:80281357 | TTTGCCTCCTCTTCC[A/G]CCTCTAGACGATCCC | 106794 |
rs108818784 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80242867 | CCTCTTGTGATGTTA[C/T]GATACATATGTACAT | 106794 |
rs108825502 | snp | A/G | | | intron-variant, nc-transcript-variant | Dhx57 | Mm_Celera | 17:80253082 | GGGGCCCACTGGGAC[A/G]TAACCTGAGGCACAG | 106794 |
rs108836390 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80278712 | TGGTATTAAAGGCGT[G/T]TGCCTCCACCACACA | 106794 |
rs108843646 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80263143 | AGGTGTGCGCCACCA[C/G]CACCTGGCTCCTAAA | 106794 |
rs108844202 | snp | A/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80266867 | AAATAAATCTTAAAA[A/T]AAAAATAAACTCTAG | 106794 |
rs108845429 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80279408 | CTTCAATGGTTTCCT[C/T]TCAGAGAGGCTCATG | 106794 |
rs108848016 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dhx57, Morn2 | Mm_Celera | 17:80290051 | CATGCCACGTCAGGC[C/T]GTACCTGGCTCGTAG | 106794 |
rs108849827 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80253889 | ATGTTGTCAAGACGA[C/T]GGGGCACAGACAAGT | 106794 |
rs108850206 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80249751 | GAAATCCATTTTGCA[C/T]AGCTGAGAAGACTGA | 106794 |
rs108851109 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80242730 | AACTCACTTTGTAGA[C/T]CAGGCTGGCCTCGAA | 106794 |
rs108855708 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80241139 | TTTCTTTCTTTCTTT[C/T]TTTCCTTCTTTCCTT | 106794 |
rs108866384 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80277151 | GAGGCAGAGGCAGGT[G/T]GATTTCTGAGTTTGA | 106794 |
rs108867850 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80269025 | ACAGGCAACGAGGAA[G/T]CCACTGCTAACTAGA | 106794 |
rs108870838 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80269028 | GGCAACGAGGAATCC[A/G]CTGCTAACTAGAGTC | 106794 |
rs108872630 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80278745 | AGCAGTGACATTTTT[A/G]AAGGGCCACTGTCTT | 106794 |
rs108886236 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80248053 | GAGGAAACATTACTA[C/G]AGCTTACTGTGAACT | 106794 |
rs108887221 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80264227 | TGTGCTCCAAGTACA[C/T]ATTAAAGCAGTGTCT | 106794 |
rs108887532 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80271601 | AAGCAGCAATCATAC[C/T]ATATCCATGTATTGA | 106794 |
rs108887807 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80277172 | CTGAGTTTGAGGCCA[A/G]CCTGGTCTATAAAGT | 106794 |
rs108891840 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80280057 | CCATCCTTCCTTTCT[C/T]TTTTGAGAAGGAAAA | 106794 |
rs108893921 | snp | A/T | | | intron-variant, upstream-variant-2KB | Dhx57, Morn2 | Mm_Celera | 17:80289626 | AGTTTGGCTCCCACG[A/T]ACAGCATCGTCAAGC | 106794 |
rs108894453 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80253896 | CAAGACGACGGGGCA[C/T]AGACAAGTGATCTTC | 106794 |
rs108899479 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80270588 | ATGTGCCTGCTTCTT[C/T]TTTTTTTTTTTTCTT | 106794 |
rs108903951 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80255858 | AAATAGTCTTACCCC[C/T]TTCCAATAGAAAACT | 106794 |
rs108904145 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80287941 | TGCTGAATGCCTCAC[C/T]CAATAACCTATGAGT | 106794 |
rs108913508 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80282157 | AATGTAAATATCTGA[A/G]ATGCAGAATAATTGA | 106794 |
rs108917216 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80264244 | TTAAAGCAGTGTCTG[A/G]GAAAATAAAACGTGG | 106794 |
rs108918949 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80269746 | ATGAATGTGCACACA[C/T]GCACACATGTATTTT | 106794 |
rs108920010 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80246775 | TAAACTTAGGCAGTC[C/T]GTGTGTGTGCGCTGC | 106794 |
rs108923441 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80246695 | ACATGTGTGTGTGTG[C/G]TTTTGCCAATTTTAA | 106794 |
rs108925337 | snp | A/C/G | | | intron-variant | Dhx57 | GRCm38.p3 | 17:80256876 | GAGTGGTAAGACAAT[A/C/G]GATAGATAGATAGAT | 106794 |
rs108926648 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80261883 | TCTCTTTTAGGACTA[C/T]CCTATTATAAGTGCC | 106794 |
rs108930950 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80284146 | CTCCCTGAGGACTGG[C/G]TTTGATGGTACCAGA | 106794 |
rs108932250 | snp | G/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80281635 | CCTTAGGACTAATAT[G/T]TAGTAAGTTTCTCTG | 106794 |
rs108933353 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80270294 | TAACGTTGGCTACAT[A/G]TCTTTTTAAAAGCAG | 106794 |
rs211751621 | in-del | -/GC | | | intron-variant | Dhx57 | Mm_Celera | 17:80272620 | ATTTGGTTTACACAT[-/GC]GTTTGATATTGGCTA | 106794 |
rs211759747 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80244367 | AGAGGGGAGTGGTAC[C/T]AAGGGAATTCTGTTC | 106794 |
rs211762827 | snp | G/T | | | intron-variant, upstream-variant-2KB | Dhx57, Morn2 | Mm_Celera | 17:80288574 | TTCCCTGGTGGGTGG[G/T]TCATTAGCTAGAATC | 106794 |
rs211764435 | snp | G/T | | | downstream-variant-500B | Dhx57 | Mm_Celera | 17:80238151 | GTTCTCCTCTTAGTA[G/T]GGTGTGGTGGAGGGA | 106794 |
rs211806872 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80271809 | CTCTTCTGATCTACG[A/G]AGGCACCTGCACACG | 106794 |
rs211814583 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80280061 | CCTTCCTTTCTCTTT[C/T]GAGAAGGAAAAACAT | 106794 |
rs212091822 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80266397 | TGTGTAACCCTGGCT[A/G]TCCCAGAACTCACTC | 106794 |
rs212120938 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80260742 | GCAATGCCCAAATCT[G/T]AATTCCTTCTTTGAG | 106794 |
rs212143193 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80260486 | CCTGCTAAAGAAGAA[A/C]GAATTTATTCTCCCA | 106794 |
rs212223991 | in-del | -/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80254497 | GAGACTGACCGACCT[-/G]TGCTGGGTACAGTTC | 106794 |
rs212224410 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80253834 | GGTTCTGGGGATTGA[A/G]CATAGTTCCTGCAAG | 106794 |
rs212241323 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80246223 | TCCCAGGGCTGTTGT[A/G]TTACTTGCTTCTTAA | 106794 |
rs212291584 | snp | A/C | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80291759 | CAGGTGGTGGGAGGA[A/C]ATTTCATCGATCTAT | 106794 |
rs212303603 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80245304 | TACTGTGACCACAGA[G/T]GAGTTTACCTCTGGG | 106794 |
rs212357737 | snp | A/T | | | intron-variant, nc-transcript-variant | Dhx57 | Mm_Celera | 17:80252635 | TATGGATATTTTGCA[A/T]TTCTTATATCATCAA | 106794 |
rs212378230 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80240442 | AAGACAGGAGCTTAC[A/G]GAGCTCAGCCTGCCC | 106794 |
rs212465995 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80273298 | CCTCCAAGAAAGGGT[C/T]TCTTTGGGTAGTTTT | 106794 |
rs212543852 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80267827 | ACTATCAAAGAGGCC[A/G]GGTGGTGGTGGCGCA | 106794 |
rs212557799 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80262388 | AAAAGTCTGATGCTC[C/G]ATTTGAAAAATACAT | 106794 |
rs212584760 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80281726 | TTTGCATGTATGGCT[A/G]CATGACAGAAGAGAG | 106794 |
rs212629800 | snp | C/T | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80290995 | CTGTAGTCATCTGAA[C/T]AAAATTGTAGACGTC | 106794 |
rs212711299 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80268344 | GGTTCCTAGCACTTA[C/T]GAGGTGGCTTACAGC | 106794 |
rs212725461 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80255972 | AAACATCTGAGAACC[A/G]AAGCAAATGCCTTGC | 106794 |
rs212826214 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80248059 | ACATTACTACAGCTT[A/G]CTGTGAACTACAGAA | 106794 |
rs212827915 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80242190 | ACAATGAGGTCAATG[A/G]CCACATAAGGGGATT | 106794 |
rs212933219 | in-del | -/A | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80266266 | TCATATTTCCATAAG[-/A]AAAAAACCACCTGAA | 106794 |
rs212966858 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80242527 | GCTCATGACCACGCG[C/T]CACTGCACGAATGAA | 106794 |
rs213020617 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80276363 | GTGACTAAGGTTACA[C/T]GGAAAGCAGCAAGAA | 106794 |
rs213113917 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Dhx57, Morn2 | Mm_Celera | 17:80289704 | TCTGACCACTATACA[-/T]TCCCCCAGCTCCATT | 106794 |
rs213140635 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80269667 | GTGACAGAGCAGGAC[G/T]TCTGACATTCTCCTA | 106794 |
rs213161851 | in-del | -/TG | | | intron-variant | Dhx57 | Mm_Celera | 17:80263010 | TATTTATTTTTATTT[-/TG]TTTATTGAGACAGGA | 106794 |
rs213318858 | in-del | -/TT | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80291170 | ATAATTATATGTATA[-/TT]TTATATATATGTATG | 106794 |
rs213362766 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80249689 | CCATGGAAGGAGGCC[C/T]ACAACAGTGTCACAG | 106794 |
rs213390722 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80283168 | TCGAGCGACCACGCC[C/T]GGCTACCTCAATACA | 106794 |
rs213480393 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80243130 | CCACGTGTTCAAGCC[C/T]CTGTGTGTGAGAGCT | 106794 |
rs213493530 | snp | A/C | | | downstream-variant-500B | Dhx57 | Mm_Celera | 17:80238089 | AGCCGCCCCGCCCAG[A/C]GCACAGGCTCGAAAA | 106794 |
rs213593203 | in-del | -/TG | | | intron-variant | Dhx57 | Mm_Celera | 17:80248449 | TTTTGTTTTGTTTTT[-/TG]TTTGTTTTGTTTTGT | 106794 |
rs213615523 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80277967 | GCCCTCACAGGGGTC[A/G]CATAGCGGATATCCT | 106794 |
rs213629699 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80270640 | ACAGGGTTCCTCTGT[A/G]TAGCCCTGGCTGTCC | 106794 |
rs213666104 | in-del | -/CG | | | intron-variant | Dhx57 | Mm_Celera | 17:80284699 | GTCCCAAGCCTCTCT[-/CG]AGACTCCAAGTATTC | 106794 |
rs213840420 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80258067 | GGGCCTGAGAAGGGA[C/G]TGTTACCTGGAGGGT | 106794 |
rs213897576 | in-del | -/TTT | | | intron-variant | Dhx57 | Mm_Celera | 17:80242666 | TCAGCAGCACCCACA[-/TTT]TTTTTTTTTTCGAGA | 106794 |
rs213934041 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80251540 | TCATGATTTATAAAT[G/T]TGATAGCTGGTAGAA | 106794 |
rs213966040 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Dhx57, Morn2 | Mm_Celera | 17:80289845 | GCCCCTCCTTTTCAA[C/T]CTTGCTCGGAGCCGT | 106794 |
rs213979652 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80239316 | CACACATGAGTGTGT[G/T]CTTGAAAATCTGGAT | 106794 |
rs213981750 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80250374 | CATTTGGCTCTTTCT[A/G]CTTCTTTCTTTTAAT | 106794 |
rs214000120 | snp | A/C | | | intron-variant, upstream-variant-2KB | Dhx57, Morn2 | Mm_Celera | 17:80288792 | AGAGTGAGTTCCAAG[A/C]CAGCCAGGGCTACAC | 106794 |
rs214106935 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80240014 | TCAGACACTCCAGAA[A/G]AGGGAGCCAGATCTC | 106794 |
rs214130051 | in-del | -/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80270008 | GGTAAGAGGAAAAAA[-/C]CCCAAGCTTTAAAAA | 106794 |
rs214223949 | in-del | -/GACAATGAG | | | intron-variant | Dhx57 | Mm_Celera | 17:80242174 | CACAAAACATCAGAT[-/GACAATGAG]GTCAATGGCCACATA | 106794 |
rs214238434 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80245071 | CTGAGATCATGACGG[C/T]GTGCCCTCAGAGGGT | 106794 |
rs214262496 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80267129 | CCACAGCTCCTCATT[G/T]CTTTCTGCTCTCAGA | 106794 |
rs214419513 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80260806 | TATAACCCTAAAGCA[A/G]CTAAATCTATCCTGT | 106794 |
rs214464062 | snp | G/T | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80291287 | AATTCATATCATGCA[G/T]CAGGTAGGAGATATT | 106794 |
rs214534803 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80282487 | AAGATGAGGGAAAGA[C/T]TTGAGAATTTATGTT | 106794 |
rs214613014 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80240502 | AAGGACTTTTGATTC[A/G]CCTTATCTTGGGATT | 106794 |
rs214640295 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80282976 | AAAGTAGCTGTTCAA[C/T]TACATAAGGAATGTT | 106794 |
rs214646414 | in-del | -/CTC | | | intron-variant | Dhx57 | Mm_Celera | 17:80267120 | TGTCGCCTTCCACAG[-/CTC]CTCATTGCTTTCTGC | 106794 |
rs214752280 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80280270 | TAAAAGCTCAGATGA[C/T]CTATGATATCATCAA | 106794 |
rs214866824 | in-del | -/A | | | intron-variant | Dhx57 | Mm_Celera | 17:80270002 | GGTGTTGGTAAGAGG[-/A]AAAAAACCCAAGCTT | 106794 |
rs214870536 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80254469 | GCACAGTAAGGACTC[C/G]GGCATGAGCCTTTGA | 106794 |
rs214886797 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80272685 | GTAAACTTGTTGCGG[C/G]GCGTAGAAAAGTCTA | 106794 |
rs214940367 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80256549 | CAGCCAGCTGTGCAG[C/T]ATGGATGTAAAACAC | 106794 |
rs214998837 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80256080 | ACCTTTTAGACCAGA[A/G]GATTGTTCTGTTAAT | 106794 |
rs215004933 | in-del | -/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80256441 | AGGCATGAGCCTCCA[-/G]TCCCCAGCTTCCTCT | 106794 |
rs215021347 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80262837 | GTACATGGTGCATGC[A/C]TGCCTGCCTGAATGG | 106794 |
rs215132010 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80284336 | CCTCATCAACAGAGG[A/G]GAAATCAGCCCTGGG | 106794 |
rs215137047 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80268362 | GGTGGCTTACAGCCA[G/T]CCACATCATCCACAA | 106794 |
rs215169370 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80283749 | TACACAGCACGTGGT[A/G]TCTGAGCAGATGACA | 106794 |
rs215305545 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80263772 | CAAAAGAGATGCAGA[A/G]ACACTAACCACAGTT | 106794 |
rs215459189 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80257530 | GTGTGCACCTTTAAT[A/C]CCAGCATTTAAAAGG | 106794 |
rs215466864 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80274127 | GGGTTTAAACCTAGA[A/G]CCTCATGGACACAGG | 106794 |
rs215505207 | in-del | -/C | | | intron-variant | Dhx57 | GRCm38.p3 | 17:80286337 | ATAAAAAATGGAAAA[-/C]AAACAAACAAACAAA | 106794 |
rs215535756 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80248138 | ATGGGAAACTGATCT[C/T]ATGAAGGTTAGCTGA | 106794 |
rs215552646 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80258215 | AAGTAAAGATCAGAA[C/G]ACTAATTCCACCTCC | 106794 |
rs215626419 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80251133 | CATTGTGCTCTGAGA[G/T]CTTTCACACCCACAC | 106794 |
rs215656962 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80278797 | ATTCGTCTTATTATG[C/T]TCCTATCTCACAGAC | 106794 |
rs215695707 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80267862 | TTTAATCCCAGCACT[C/T]GGGAGGCAGAGGTAG | 106794 |
rs215748553 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80242560 | GGTCAGAGGACGACT[A/G]GCAGCATCCAGTTCT | 106794 |
rs215793370 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80277068 | AAATAAATGTTGAGG[A/G]AAAAAAAAAAAAAAG | 106794 |
rs215810097 | in-del | -/TTG | | | intron-variant | Dhx57 | Mm_Celera | 17:80257025 | TGTTGTTTGTTTGTT[-/TTG]TTGTTGTTTGTGAGG | 106794 |
rs215821840 | in-del | -/TTTTC | | | intron-variant | Dhx57 | Mm_Celera | 17:80253519 | TGCCACCTCTAGCTT[-/TTTTC]TTTTCTTTTCTTTTT | 106794 |
rs215841224 | in-del | -/AGAAAAATAACTCAGT | | | intron-variant | Dhx57 | Mm_Celera | 17:80240943 | TAATGTGCAAAGAGA[-/AGAAAAATAACTCAGT]AGCTTTTCATATTGA | 106794 |
rs215878504 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80247485 | GGTTCAGAGGTGGGA[A/G]CATGGCAGCAGCCAG | 106794 |
rs215949842 | in-del | -/AAAT | | | intron-variant | Dhx57 | Mm_Celera | 17:80271888 | TACTCTTTAAAAATA[-/AAAT]AAAAATTTTAAATGG | 106794 |
rs215974704 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80269731 | TGTACAAGCCCCAAC[A/G]TGAATGTGCACACAC | 106794 |
rs216079710 | snp | C/T | | | intron-variant, nc-transcript-variant | Dhx57 | Mm_Celera | 17:80252530 | CTTGACCACCGTGCA[C/T]AGCACTTAAAAAGAG | 106794 |
rs216115508 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80242964 | GTCTATAGGGGTCAG[A/G]AAAGGGCACTGGATC | 106794 |
rs216117161 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Dhx57 | Mm_Celera | 17:80260337 | GTCTTCCTCTACCTC[C/T]TCCTGTGCAGTTCTG | 106794 |
rs216225346 | in-del | -/CA | | | intron-variant | Dhx57 | Mm_Celera | 17:80263904 | TAAAAAGGAAGGTAG[-/CA]CCCTGGCACACTCAG | 106794 |
rs216244264 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80272762 | AGATCTTGTCTCAAA[A/G]TGAGAAAAAAGAAAA | 106794 |
rs216276654 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80280360 | GATATGTATGGCTAA[C/T]AAAGTCTCTCTACCT | 106794 |
rs216291944 | in-del | -/AGATGCAGTCA | | | intron-variant | Dhx57 | Mm_Celera | 17:80243875 | TGTGTTCTCTAAGTC[-/AGATGCAGTCA]AGATGAGTCAGATGA | 106794 |
rs216323284 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80270351 | GCCTTGCACGTACAC[A/G]TAAGCCACTTCTTAC | 106794 |
rs216326823 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80243486 | GAACGTCATCCTATT[A/G]CCTTCTTACATATCC | 106794 |
rs216502237 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80273911 | ATATCTGTGTTTGCC[C/G]GGCATAAGAAAAACC | 106794 |
rs216513913 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80271012 | TCAACACTGTAGTAA[A/G]TATTTATGTGTCCAT | 106794 |
rs216658169 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80255843 | GATTTAATAAGGACA[A/G]AATAGTCTTACCCCT | 106794 |
rs216690722 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80254608 | TGTGGCCTTATTGGA[A/G]GTGTAGCTTTGTTAG | 106794 |
rs216786531 | in-del | -/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80238972 | TGGGAGGCTTTCATA[-/G]CAAAGCATCTGACTG | 106794 |
rs216843345 | snp | G/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80283019 | CCATATGCTAACCTG[G/T]AAAACAAACCTCACT | 106794 |
rs216900088 | snp | C/T | | | downstream-variant-500B | Dhx57 | Mm_Celera | 17:80238128 | CAGAGAGTGAGACCC[C/T]GAGGATTGTTCTCCT | 106794 |
rs217038735 | in-del | -/TCCCCAGAGGTTAAAAA | | | intron-variant | Dhx57 | Mm_Celera | 17:80243387 | CAGTGACCTTTCGGT[-/TCCCCAGAGGTTAAAAA]TCTCAACTCCCTACA | 106794 |
rs217185250 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80271747 | CAGCACCCACATCAG[A/G]TAGCTCACAACCATC | 106794 |
rs217194968 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80248184 | GAGACGGAGTGTGCC[A/G]CTGCTCCCTGGCTCC | 106794 |
rs217203150 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80243392 | GACCTTTCGGTTCTC[A/C]ACTCCCTACATGACC | 106794 |
rs217241136 | in-del | -/A | | | intron-variant | Dhx57 | Mm_Celera | 17:80241345 | CGCCCGGTTCTTTTT[-/A]TTTTTTATAAGATAA | 106794 |
rs217283426 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80277875 | GTAACTGCTCTTCTA[G/T]CTCTCTTGCCTCACT | 106794 |
rs217300270 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80240399 | GTGTGAGCCACCACG[C/T]CCGGCCAGATTTTTG | 106794 |
rs217300526 | snp | G/T | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80290825 | TATATTAACATATAA[G/T]ATATTAATATTATTT | 106794 |
rs217446567 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80240040 | ATCTCATTTCGGATG[A/G]TTGTGAGCCACCATG | 106794 |
rs217467031 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80270906 | GAGGCGGCAGAGCAA[C/T]CTGTACAGTTGTACA | 106794 |
rs217511650 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80245164 | GAGAAAGTCTGGAAA[A/G]GTACACAGTGACTGG | 106794 |
rs217621812 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80267799 | GCCATACACTCTTCC[A/G]CTTCACATTAAAACT | 106794 |
rs217771910 | snp | C/T | | | intron-variant, nc-transcript-variant | Dhx57 | Mm_Celera | 17:80252124 | TGTGGGAATCCAAGC[C/T]GGACCTGGTGGCACA | 106794 |
rs217775386 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80260893 | TAATCAAACACACAG[C/T]AAGACTCTCACTAGA | 106794 |
rs217800010 | in-del | -/A | | | intron-variant | Dhx57 | Mm_Celera | 17:80273793 | CAACTCTAAAACATT[-/A]AAAAAAAAGCTATTG | 106794 |
rs217870404 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80261659 | AACAGAATGCTGCCC[A/G]AGGAGCAGCGGCTGA | 106794 |
rs217877974 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80267226 | GTCAACGCTTTAAGT[A/T]CCCGAGTGAATGCTT | 106794 |
rs217959049 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80271048 | TGATACATACATACA[C/T]TGTCCAATAGAGTAA | 106794 |
rs218068450 | snp | A/G | | | synonymous-codon | Dhx57 | Mm_Celera | 17:80241955 | CTGTCCCTTTACCTG[A/G]TGGGAGGCGGCCACA | 106794 |
rs218095611 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80240118 | CTTAACTGCTAAGCG[A/G]TCTCTCCAGCCCGGA | 106794 |
rs218202223 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80272918 | GGGAGGTGGCGCTGG[C/T]CCTTAAACAGTACCT | 106794 |
rs218204039 | in-del | -/CTAAC | | | intron-variant | Dhx57 | Mm_Celera | 17:80241765 | ACCTCTGTAGCAGTT[-/CTAAC]CCAGCCAGGGGTCGC | 106794 |
rs218218071 | snp | A/C/T | | | intron-variant | Dhx57 | GRCm38.p3 | 17:80241322 | GGGATTAAAGGCGTG[A/C/T]GCCACCACGCCCGGT | 106794 |
rs218231365 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80272469 | TATCTGTGTCACCTC[A/G]GGCACACTGTAAGCC | 106794 |
rs218262758 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80267293 | ACTACCCCACAGGAG[C/T]ATGGCATGATGCCCA | 106794 |
rs218300213 | snp | A/C | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80266936 | TTCCCGTTCTTCCCC[A/C]CCTGCTGTCTTCTCT | 106794 |
rs218330775 | in-del | -/A | | | intron-variant | Dhx57 | Mm_Celera | 17:80246344 | TATAACTTCACCATT[-/A]AACTTTATTATTTAT | 106794 |
rs218650266 | in-del | -/GG | | | intron-variant, upstream-variant-2KB | Dhx57, Morn2 | Mm_Celera | 17:80289308 | TTGAGAAATGGCTGA[-/GG]GGAAAAAAAAAAGGC | 106794 |
rs218757065 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80240663 | GAAGCTTTCATGAAA[C/T]TTCTAGCCATGCGGC | 106794 |
rs218846806 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80257402 | TGAGAGAGCAGCCAT[C/T]ACCATTGCTCCTAAG | 106794 |
rs218929010 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80268091 | AGTGTCCTAGAGCTC[A/G]CCCTATAGAACAGGC | 106794 |
rs218971167 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80242343 | TTAGGGCTGGGAATG[G/T]AGCTCAGTACCAGAA | 106794 |
rs218998208 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80284369 | TGAAAACCAGGCGAG[C/T]TCCTCACGGACGTCA | 106794 |
rs219034584 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80243085 | CTTGATTCTTTCTCT[C/T]TACACCTCCTCATTT | 106794 |
rs219065859 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80284840 | TCACTCTACTTTGAG[C/T]TCTGAAATCTATCAG | 106794 |
rs219098492 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80242710 | TGTAGCCCTGGCTGT[A/C]CTGGAACTCACTTTG | 106794 |
rs219150558 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80269379 | GGGATATGAACGCTA[A/C]AGAAGGATCCCAAAG | 106794 |
rs219157665 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80282715 | AACAACTCTAAGAAA[-/T]GGGGAAATAGATAAT | 106794 |
rs219273968 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80269971 | AGAGTATGCAACAGG[A/G]AAAAAATGTTACTCA | 106794 |
rs219334624 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80264477 | ATAAGTTCTAATGAT[C/T]GTTTCCCCATCATGC | 106794 |
rs219362296 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80264060 | GTGTGAAGCTGGAGC[C/T]TGTGTGTGTGTCTCT | 106794 |
rs219388190 | in-del | -/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80260633 | GTCATTGTTTCTGTC[-/T]AATGTTCTTATCTAA | 106794 |
rs219393798 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80258236 | TTCCACCTCCCACCT[G/T]GAGGTTTGCGAGTGT | 106794 |
rs219433584 | in-del | -/A | | | intron-variant | Dhx57 | Mm_Celera | 17:80267958 | AGAAACCCTGTCTCG[-/A]AAAAAAAAAAAAAAA | 106794 |
rs219458503 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80258747 | CGGATCATCTAGAAG[C/T]CCAGGTAACAATTAG | 106794 |
rs219511116 | in-del | -/TTAT | | | intron-variant | Dhx57 | Mm_Celera | 17:80239108 | TAGCACATTTATTTA[-/TTAT]TTATTTATTTAGAGA | 106794 |
rs219533763 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80264317 | TTGACTCAGGGTCTC[A/T]CTACATAGCTCTGGT | 106794 |
rs219601157 | in-del | -/TTGCCTGGC | | | cds-indel, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80281385 | CCCTTTCCATCCCCT[-/TTGCCTGGC]TTGCCTTTTCTTCTT | 106794 |
rs219630110 | snp | C/T | | | intron-variant | Dhx57 | GRCm38.p3 | 17:80286568 | AGGAACTATATGCAG[C/T]TATAGAATGCTGAGA | 106794 |
rs219686205 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80243562 | TCCTGTGCTGGAATA[A/T]TCTCTCCTTAGAGAT | 106794 |
rs219813450 | in-del | -/GGGAAC | | | intron-variant | Dhx57 | Mm_Celera | 17:80274184 | TCTAGCCCTTAGCCA[-/GGGAAC]TCTTTTGAAAGATGG | 106794 |
rs219917745 | snp | C/T | | | utr-variant-3-prime | Dhx57 | Mm_Celera | 17:80238469 | ATGCATAATAAAAAA[C/T]AGGAGGGAAAGGATA | 106794 |
rs219952330 | snp | G/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80265413 | CAAAATGTAATAGGA[G/T]TATCACTGAAGTTGA | 106794 |
rs220044928 | in-del | -/TA | | | intron-variant | Dhx57 | Mm_Celera | 17:80239417 | TATAGTCCCACACTG[-/TA]GCCCAGACTGGCCTC | 106794 |
rs220061627 | in-del | -/TATGTATATATG | | | intron-variant | Dhx57 | GRCm38.p3 | 17:80286780 | ACATATATGTATATA[-/TATGTATATATG]TGTGTGTGTATATGT | 106794 |
rs220093456 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80240221 | ATAACTGCTGAGCCA[C/T]CTCAGATTTTTGGTT | 106794 |
rs220107239 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80259099 | AATCTACAAACTTCC[G/T]ACCCACTGGAGTCAG | 106794 |
rs220149894 | snp | A/C | | | intron-variant, upstream-variant-2KB | Dhx57, Morn2 | Mm_Celera | 17:80289038 | TAATCGCATTCTCCC[A/C]CCCCCCTCCCCCCAC | 106794 |
rs220155562 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80266998 | CTCAGTCCACAGTGT[C/T]CATCCAAGCTGTCTC | 106794 |
rs220159447 | in-del | -/A | | | intron-variant | Dhx57 | Mm_Celera | 17:80264418 | GTGCTGGTAGTGCTT[-/A]AAAAATATTCTTTAA | 106794 |
rs220190218 | in-del | -/TC | | | intron-variant | Dhx57 | Mm_Celera | 17:80276463 | CTACCCCTGTCCCTT[-/TC]CCCTCTTCTAAGACT | 106794 |
rs220270178 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dhx57, Morn2 | Mm_Celera | 17:80289048 | CTCCCACCCCCCTCC[C/T]CCCACCTTTATGTCT | 106794 |
rs220316057 | snp | C/G | | | intron-variant | Dhx57 | GRCm38.p3 | 17:80252267 | TCCACCTGCCTCTGC[C/G]TCCCGAGTGCTGGGA | 106794 |
rs220322145 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80261724 | GCCATGCGCTCTGGT[C/T]GAGTCAGCTTAAGCC | 106794 |
rs220343796 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80279771 | CGCAGAAGTGAGGTC[G/T]TAACCCAGTGGGTGA | 106794 |
rs220368862 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80239433 | AGCCCAGACTGGCCT[C/T]GAACTCACAGAAAGC | 106794 |
rs220406218 | in-del | -/C | | | intron-variant | Dhx57 | GRCm38.p3 | 17:80286366 | AACAAACAAAAAAAA[-/C]CAAAGGGATTGTGAG | 106794 |
rs220406282 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80261122 | TCCTCTGGAGGTCTA[A/G]GGTTTCTCAGAGGCC | 106794 |
rs220441344 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80259855 | TAAGGACGCACTCCT[C/G]GCATGACACTCTGCA | 106794 |
rs220455195 | snp | A/C | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80281816 | GCAGCCAGTGTTCTT[A/C]CCTGTCCAGCTCCAG | 106794 |
rs220633370 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80283301 | GAAATTTAAAACTAG[A/C]TCTCTTAGTACTTTT | 106794 |
rs220665952 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80282800 | TGGCTTTTTTTTTTT[C/T]CCCACAGACAGGGTT | 106794 |
rs220666023 | snp | A/T | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80292475 | ATTGAAAGTTTTCAA[A/T]TTTTTCTCTAGAAAT | 106794 |
rs220817551 | in-del | -/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80258998 | GCTCTACACAGTGAG[-/T]CCCAGGTCCTCTTTG | 106794 |
rs220866619 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80281943 | TTCAAGGCCAGCCTG[A/G]TCTACAGAGTGAGTT | 106794 |
rs221032594 | in-del | -/GA | | | intron-variant | Dhx57 | Mm_Celera | 17:80279688 | AATAGATAGCTAATG[-/GA]TACTTGAACAGGCAG | 106794 |
rs221068021 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80262605 | GCTAAAAATCTGATA[A/G]ACAGCAAGGGTGGGT | 106794 |
rs221183634 | snp | A/T | | | synonymous-codon, nc-transcript-variant | Dhx57 | Mm_Celera | 17:80275467 | CAAGCTCACATAAAC[A/T]GCTGCCTCAGAGAGC | 106794 |
rs221196344 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80263130 | GTGCTGGGATTAAAG[A/G]TGTGCGCCACCACCA | 106794 |
rs221197475 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80256386 | GCTGTCCTTTAGCCT[A/G]TGTAGCGTCTCCTGC | 106794 |
rs221387921 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80258916 | TCTGGGCATAGTGTT[G/T]CAGGCCTTTAACCTT | 106794 |
rs221396614 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80284030 | AGCCACAAATTTATG[G/T]TTGCACCCTAGAGGT | 106794 |
rs221399728 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80250906 | GACTGTGCGTGCAGA[C/T]TACCTTTCTATTGAG | 106794 |
rs221492203 | snp | C/T | | | intron-variant, downstream-variant-500B | Dhx57 | Mm_Celera | 17:80251764 | ACTGGGAACTGAACT[C/T]AGGTCCTCTGCAAGA | 106794 |
rs221510518 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80284455 | ACTACACTGCAAATA[C/T]TCATAGCCACAGGTT | 106794 |
rs221511508 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80248499 | GTTTTTCTCTGTGTA[A/G]CCCTGGCTGTCCTGG | 106794 |
rs221515668 | snp | G/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80282768 | GGCAGAGCAAGCTCA[G/T]GGGCATTTAGGAGAG | 106794 |
rs221564946 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80288196 | GTGGGGAGGAAGACA[G/T]AGGGTGTTTACATCG | 106794 |
rs221611850 | snp | A/G | | | intron-variant | Dhx57 | GRCm38.p3 | 17:80256752 | AGGAGACACTCCTCA[A/G]CCCTTGGCTAGGCCT | 106794 |
rs221637335 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80279015 | TCTTAAAGCCCCAGT[A/C]TATTTGGAGACTATC | 106794 |
rs221952196 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80256306 | ATGTTTCTGTCCTAA[C/T]CGCAGTCTTTCCCCA | 106794 |
rs222148732 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80247859 | TGTCAGATCTCATTA[C/T]GGGTGGTTGTGAGCC | 106794 |
rs222235628 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80256274 | AAAGAAAATAAGCAA[A/C]AATAAGAGATTATAG | 106794 |
rs222247436 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80247069 | ATTTAAAGTTACTAA[C/T]AGAACAAAAACCAGG | 106794 |
rs222319805 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80259949 | GTCCTCCGTTACTAC[C/T]TTGCCTTTGTCCTTA | 106794 |
rs222328329 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80255203 | AGCTAGCTTTGCCCT[C/T]CTATGTGACGGCACA | 106794 |
rs222367587 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80250816 | CTTATACAGAACCCA[A/G]ACCTTTTCCTCCCTC | 106794 |
rs222524890 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80257743 | TGGTTTGTCAAGACA[A/G]GGTCTGTCTGCATAG | 106794 |
rs222557757 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80253917 | AGTGATCTTCCACCT[G/T]ATTCCTGAGCTGTAC | 106794 |
rs222585014 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80271142 | ATTTTAATGAGTAAA[C/T]TTGACTGTAAATGGC | 106794 |
rs222610209 | in-del | -/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80244730 | GCAGAAGGCTACAGA[-/G]CATTCCAGATTATTG | 106794 |
rs222630770 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80249968 | ATCAAGCTGAACTTA[C/T]TGACATTGGTGCCAG | 106794 |
rs222633089 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80278916 | TTCTGTAACCATGGA[C/T]CTGCTCAGTGGATCC | 106794 |
rs222671389 | snp | C/T | | | missense, upstream-variant-2KB, nc-transcript-variant | Dhx57 | Mm_Celera | 17:80281418 | CTTCTTACTGAAGAA[C/T]TCATTTTCACCTGAA | 106794 |
rs222672303 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80269202 | ACCTTCGGAGGAGCA[A/G]TCAGTGCTCTTACCC | 106794 |
rs222693156 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80246593 | CCTAATAGCTCTAGA[A/G]ATGGGGCACAGATAG | 106794 |
rs222746528 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80273588 | TATACTATGACATGT[A/G]AGAGAAAGCTTTGAG | 106794 |
rs222746702 | snp | A/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80282684 | ACCTAACAGTGAAAC[A/T]CGCAACTTCACAAAG | 106794 |
rs222777079 | in-del | -/CCGTT | | | intron-variant | Dhx57 | Mm_Celera | 17:80249059 | TTGATTTACGTTTAA[-/CCGTT]CTGTTTGTGTTTCTA | 106794 |
rs222786343 | snp | A/G | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80281854 | AGCCAAGAATGTACT[A/G]CAGAGACATATGGGG | 106794 |
rs222826653 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80278596 | CTGTTTGTTTGTTTG[G/T]TTGCTTATTTGGTTT | 106794 |
rs222885427 | in-del | -/AA | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80291513 | CAAACAAACAAAACC[-/AA]AAAAAAAAAAAAACC | 106794 |
rs222911128 | in-del | -/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80259800 | AAATAAAATGACATC[-/T]TTTAAAACCGTCCCC | 106794 |
rs223000610 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80271903 | AAAAAATTTTAAATG[A/G]AATATAAGCTTTGCG | 106794 |
rs223007246 | snp | A/T | | | intron-variant, nc-transcript-variant | Dhx57 | Mm_Celera | 17:80252298 | TCAAAGGTGTGCGCC[A/T]CCACCACCTGGTTTT | 106794 |
rs223173394 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80244745 | ACATTCCAGATTATT[A/G]TAGTACTTTGGGCAC | 106794 |
rs223243973 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80250350 | CCGCTCTTTTTTTTC[A/T]GGCTCTGTCATTTGG | 106794 |
rs223347738 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80273117 | ATCTTTCCCCTTGAA[C/T]GGAGCGAAAGGAAAC | 106794 |
rs223373878 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80243397 | TTCGGTTCTCAACTC[C/G]CTACATGACCTGACC | 106794 |
rs223374272 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80250935 | AGTTACTTTTCACAG[C/T]TGATGCATGTGTTCA | 106794 |
rs223380824 | in-del | -/G | | | intron-variant, upstream-variant-2KB | Dhx57, Morn2 | Mm_Celera | 17:80288503 | TGAGTGGTAGATAAA[-/G]GGTGGTGGTTTGAGA | 106794 |
rs223417139 | in-del | -/A | | | intron-variant | Dhx57 | Mm_Celera | 17:80251202 | TGAGAACTGTGACAT[-/A]AAATTCCAATTTAGA | 106794 |
rs223444655 | snp | A/T | | | intron-variant, nc-transcript-variant | Dhx57 | Mm_Celera | 17:80252810 | TAATGAGGCTGTAGA[A/T]TTTTCCCTGGCATAC | 106794 |
rs223536654 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80270935 | CAAAGCTAAATGCAC[G/T]GAGAGGTATGAACCG | 106794 |
rs223582241 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80249813 | CAACTGCCAGCTACG[A/C]CAGCGAGATGATGAG | 106794 |
rs223592277 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80273424 | AGTTTCAATTCAAGG[A/G]ATTAACATAGAATGT | 106794 |
rs223715586 | in-del | -/TCTT | | | intron-variant | Dhx57 | Mm_Celera | 17:80253585 | CCTCCTTCTCTCCCC[-/TCTT]TCTTTCTTTTCTCTT | 106794 |
rs223716707 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80250670 | TCTGCTTCCAGAATA[A/T]AAGATCATCACACCT | 106794 |
rs223736802 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80267314 | ATGATGCCCAGGAGA[C/T]ACTCCTGGTGATGGG | 106794 |
rs223861329 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80243524 | TGACAGATATACTCT[C/T]ACTCCTGGCCTCAGC | 106794 |
rs224030909 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80247043 | GCACCACCACTGCTC[A/G]GCATGAATAAATTTA | 106794 |
rs224038161 | in-del | -/CG | | | intron-variant | Dhx57 | Mm_Celera | 17:80263744 | TAGTCACACTCCATC[-/CG]CGCACCGGATGCAAA | 106794 |
rs224089033 | in-del | -/A | | | intron-variant | Dhx57 | Mm_Celera | 17:80250329 | AAAAGACAAGCCATC[-/A]AAGGACCGCTCTTTT | 106794 |
rs224161354 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80268624 | CGAGGGATTTGAACC[C/G]CACGGAAAGTGGCTA | 106794 |
rs224190344 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80275618 | CTGCCGAGGGCAAAA[C/T]ATGACAAAGATGCTG | 106794 |
rs224277611 | in-del | -/AC | | | intron-variant | Dhx57 | Mm_Celera | 17:80247379 | TAGAATTAAAGATGT[-/AC]ACTACTGCCTTAGTT | 106794 |
rs224378131 | in-del | -/TGAGTCCCAGGTCCTCTT | | | intron-variant | Dhx57 | Mm_Celera | 17:80258994 | GTTTGCTCTACACAG[-/TGAGTCCCAGGTCCTCTT]TGACCCCACCCGTCA | 106794 |
rs224528103 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80246790 | TGTGTGTGTGCGCTG[C/T]AGGCTCATTTATAAC | 106794 |
rs224609699 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80242735 | ACTTTGTAGACCAGG[C/T]TGGCCTCGAACTCAG | 106794 |
rs224644317 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80243245 | ATTCTCACGACCTTC[A/G]ACCTTCGTAGCTACT | 106794 |
rs224657227 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80244993 | CTAGCTGCTATTCTC[C/T]AGCAGGAAAGTTCAG | 106794 |
rs224726100 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80264076 | TGTGTGTGTGTCTCT[C/G]TGTGTGTGTGTGTGT | 106794 |
rs224728935 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80240349 | TCGAACTCAGAAATC[C/T]GCCTGCCTCTGCCTC | 106794 |
rs224787499 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80239744 | GATTCCTGGAACCAG[A/C]GTTACAGACAGTTGT | 106794 |
rs224844366 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80241842 | CTCATGTTGCTTTCA[C/T]GCTTCCTGCCCATTA | 106794 |
rs224853320 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80273163 | TTTCTTTAGGCAAGG[A/G]ATAACACCACTAACA | 106794 |
rs224869881 | snp | C/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80270707 | CAGAAATCCGCCTGC[C/G]TCTGCCTCTGCCTCC | 106794 |
rs224972540 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80267102 | TCTCTGACTGTCTTA[C/T]AGTGTCGCCTTCCAC | 106794 |
rs225039533 | in-del | -/GC | | | intron-variant | Dhx57 | Mm_Celera | 17:80242937 | ATGTGTGTTTTGCCT[-/GC]ATATATTTGTGTCTA | 106794 |
rs225055957 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80243581 | CTCCTTAGAGATCTG[C/T]ATGGCTTGTTTTTAA | 106794 |
rs225228997 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80271402 | AGGACGGAAAGCCTG[G/T]AATGCTCTATAGCAT | 106794 |
rs225263902 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dhx57, Morn2 | Mm_Celera | 17:80288924 | AGCCCCAACCACGAG[C/T]TCTCCAAAGGACAGC | 106794 |
rs225277285 | snp | C/T | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80291780 | ATCGATCTATGGTCC[C/T]TATTTTAGTGTAGGT | 106794 |
rs225325048 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80284261 | GTGCAATCACCCTAA[G/T]GGGGGAATAGTGGCA | 106794 |
rs225410835 | snp | A/G | | | utr-variant-3-prime | Dhx57 | Mm_Celera | 17:80238577 | AGAAAGACAAGCTGG[A/G]TTTTAGGCTGTCCTA | 106794 |
rs225553688 | in-del | -/TC | | | downstream-variant-500B | Dhx57 | Mm_Celera | 17:80237820 | TTTTTTTTTTTTTTT[-/TC]CGAGACAGGGTTTCT | 106794 |
rs225576317 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80260565 | TTACCTTCGTAGCAG[A/G]CCAGGATTCTGCTGG | 106794 |
rs225617013 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80265975 | TCTTTCTTGACTACT[C/T]AAAACATGTTCGGCA | 106794 |
rs225658324 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80271966 | CGAGGCAGAGGCAGG[C/T]GGATCTCTGTAAGTT | 106794 |
rs225669170 | in-del | -/A | | | intron-variant | Dhx57 | Mm_Celera | 17:80280814 | GAATTCAACCTATTT[-/A]AAAAAATAAAAACCC | 106794 |
rs225716445 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80240607 | ACAAATTCAAAATGA[A/G]CCACCCACCTCAACA | 106794 |
rs225803930 | in-del | -/AGGAAATCTGGAGG | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80281799 | CTGGGAATTAAATTC[-/AGGAAATCTGGAGG]AGCAGCCAGTGTTCT | 106794 |
rs225918181 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80267979 | AAAAAAAAAACCAAC[A/T]ATGAAAGACTCTCTC | 106794 |
rs225968176 | snp | C/G/T | | | downstream-variant-500B | Dhx57 | GRCm38.p3 | 17:80238099 | CCCAGAGCACAGGCT[C/G/T]GAAAATGTACAAGCA | 106794 |
rs225981069 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80243333 | CGCTGTTGCTGCTTC[C/T]ACGTCTTACAGTGTC | 106794 |
rs226015495 | in-del | -/TGTCAGCTTCTAAGCATATGC | | | intron-variant | Dhx57 | GRCm38.p3 | 17:80240628 | ACCTCAACATGCAAG[-/TGTCAGCTTCTAAGCATATGC]CACTCCCACACGTTA | 106794 |
rs226050235 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80261839 | TAATTTTCCATTCCC[A/G]CGTTAGTCTAGTGTA | 106794 |
rs226054214 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80245390 | GCAAATCCCACATGC[A/G]GATGGAGGGATTACC | 106794 |
rs226102471 | snp | C/G | | | synonymous-codon | Dhx57 | Mm_Celera | 17:80238925 | TTCCTTCACCAGCTC[C/G]GCCACCTATGATGGC | 106794 |
rs226115954 | snp | A/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80264754 | CTCAGTGTCTGGGTA[A/T]GTAGCACAATCCATA | 106794 |
rs226218803 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80240318 | CCTGGAACTCACTTT[A/G]TAGACCAGGCTGGCC | 106794 |
rs226220429 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Dhx57 | Mm_Celera | 17:80260274 | TTGATCAGGTATTGT[A/G]TCTTTGACAGACTCC | 106794 |
rs226259339 | snp | C/T | | | intron-variant, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80266109 | TATTTTACTTATTCG[C/T]TTTATTATTGGGCTC | 106794 |
rs226381584 | in-del | -/CT | | | intron-variant | Dhx57 | Mm_Celera | 17:80261536 | AGAAGTGCCTAAGCC[-/CT]CTAAGGACCAAGCAG | 106794 |
rs226465751 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80283372 | TCCTCTCCTACGCCT[A/C]GAAAGCTCTTTGGAG | 106794 |
rs226476212 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80287884 | ATAAAAAGGTTCTAA[A/C]AAAAAAAATTATTTA | 106794 |
rs226485936 | snp | G/T | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80291610 | GGAAATCTGAAGAGC[G/T]GTTGAGGACTGCTTC | 106794 |
rs226493796 | snp | C/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80242321 | ACGCTTTGCAGACCG[C/T]TCCTTCTTAGGGCTG | 106794 |
rs226570814 | snp | A/T | | | upstream-variant-2KB, intron-variant | Dhx57, Morn2 | Mm_Celera | 17:80290753 | AAAACACAAGTACAG[A/T]TTTCAAAAATTAAAC | 106794 |
rs226638487 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80263411 | AACATCCTAACATTC[A/C]GCGCATATTACAAAC | 106794 |
rs226640785 | in-del | -/CTCT | | | intron-variant | Dhx57 | Mm_Celera | 17:80267988 | ACCAACTATGAAAGA[-/CTCT]CTCTCTCACACACAC | 106794 |
rs226697331 | snp | A/G | | | intron-variant | Dhx57 | Mm_Celera | 17:80262490 | AGAGACCCATTCCAC[A/G]CAGACAAAGGGGCCC | 106794 |
rs226748295 | in-del | -/GCAGCT | | | cds-indel, upstream-variant-2KB | Dhx57 | Mm_Celera | 17:80281291 | GCCGCCTCCGCCGCC[-/GCAGCT]ACCGCCGCCGCCACC | 106794 |
rs226780676 | snp | G/T | | | intron-variant | Dhx57 | Mm_Celera | 17:80241733 | TCTCGCCTCAGCTTC[G/T]AATCTACTTGACTCA | 106794 |
rs226874373 | in-del | -/C | | | intron-variant, upstream-variant-2KB | Dhx57, Morn2 | Mm_Celera | 17:80288621 | CCTAGGTGAGTGGGA[-/C]CCCCCCTCCCCACAA | 106794 |
rs226886729 | in-del | -/AAAC | | | intron-variant | Dhx57 | Mm_Celera | 17:80255668 | GAATAAAGAACGAAT[-/AAAC]AAACAAACAAACAAA | 106794 |
rs226985917 | snp | A/C | | | intron-variant | Dhx57 | Mm_Celera | 17:80284648 | CAGGAAGGAGAGGCT[A/C]ATACGTAGATCCCTG | 106794 |