SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3021894 | snp | A/G | 0.71875 | 0.0826797 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74704843 | GGTATGTGTTCTCCC[A/G]TGACAGCTTTCAGTT | 18472 |
rs3023299 | in-del | -/T | | | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74724975 | GTCTTTCTGTGGATT[-/T]CAGTTTCCAGAATCT | 18472 |
rs3023300 | snp | C/T | 0.4352 | 0.167931 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74709216 | TCAGCCTCCAAGAGC[C/T]GGGGTGTGTTCTACT | 18472 |
rs3023301 | snp | C/T | 0.382461 | 0.212024 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74709010 | CTGGTGACTGCCTTT[C/T]CCAGCTGTTTGCTAT | 18472 |
rs3023302 | in-del | -/TAGT | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74708404 | CATAAGTGTGGATAA[-/TAGT]TAGAAACCAGTTGAG | 18472 |
rs3023303 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74708366 | ACTTTTATAACTTAT[A/G]AGCAGTTGCTGTGAG | 18472 |
rs3023304 | in-del | -/AAAC | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74708315 | TCATACCCTAGAGAA[-/AAAC]AAACATCTTGGGGCT | 18472 |
rs3023305 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74704701 | AGTCAAGAAATAGTG[A/G]CTGGGCAGTGGTGGC | 18472 |
rs3023306 | in-del | -/ACACAC | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74704574 | AAAAACAAAAAACAA[-/ACACAC]ACACACACACACACA | 18472 |
rs3023307 | snp | C/T | 0.5 | 0 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74704476 | GACTCGTGTTTGATT[C/T]CCAGAAGCCACATGT | 18472 |
rs3023308 | snp | C/T | 0.5 | 0 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74704447 | GTTGGCTCATACTAT[C/T]TTACTCCAATCCAGG | 18472 |
rs3023309 | snp | C/T | 0.399209 | 0.200591 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74701116 | CCAGGCATGTTGATG[C/T]ATTCCTGTAATCCAG | 18472 |
rs3667338 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Pafah1b1 | Mm_Celera | 11:74721280 | TTGTGATTTTTAAAA[C/T]TGATTCCATCAAATT | 18472 |
rs3679167 | snp | A/G | 0.5 | 0 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74701956 | AAGCAATGAGCGGAC[A/G]CTTGGAAAAATCTGA | 18472 |
rs3679320 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74702038 | CTCTTAGTTTTATCT[A/G]ATTAGGTATTTTGCA | 18472 |
rs3691128 | snp | G/T | 0.433884 | 0.169371 | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | GRCm38.p3 | 11:74675986 | GCTAGACAGTGAGCT[G/T]CTGTCAGAGCCTAAT | 18472 |
rs3692341 | snp | C/T | 0.495 | 0.0497494 | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74676172 | GTTATGTCATTGTTT[C/T]TGTTAACCTTTCAAA | 18472 |
rs4139851 | snp | A/T | 0.5 | 0 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74702148 | ctctctctctctctc[A/T]cacacacacacacac | 18472 |
rs4140077 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Pafah1b1 | Mm_Celera | 11:74721225 | CAGGACAGCCAGGGA[C/T]ACACAGAGAAACCCT | 18472 |
rs6173900 | snp | A/G | 0.5 | 0 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74701738 | TTCAAAGACAAGTtg[A/G]ctcaaacctccaatc | 18472 |
rs6362714 | snp | C/G | 0.498615 | 0.0262793 | intron-variant | Pafah1b1 | Mm_Celera | 11:74697723 | AGACACTATGGCAAA[C/G]TAAAGGATTATTTTT | 18472 |
rs6363729 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74697882 | tgtagagatggctca[A/G]ccatctgctcctctg | 18472 |
rs6364260 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74697960 | TTTGTAATGAGATCC[A/G]ATGCCCTCTTCTGGG | 18472 |
rs8236871 | snp | C/T | 0.1472 | 0.227886 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74682068 | TAGAATGCATTGTTA[C/T]AGAAAATAAATCTAT | 18472 |
rs8236872 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74682176 | GCATTTACCTTTTTG[A/G]ATCAGATAGACTTGT | 18472 |
rs8236873 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74682192 | TTGGCATCTTCATTG[C/T]GCATTTACCTTTTTG | 18472 |
rs8236874 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74699177 | CCTGGGCTACCTGAA[A/G]TCTTATCACAAAAGA | 18472 |
rs8237703 | snp | A/G | 0.42 | 0.183303 | intron-variant | Pafah1b1 | Mm_Celera | 11:74709180 | TTCTTAGTGTTATGG[A/G]TTTTACTAATTCCTG | 18472 |
rs8237704 | snp | C/T | 0.595041 | 0.156807 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74701133 | TAAACATTGTTTTCT[C/T]gccaggcatgttgat | 18472 |
rs8237707 | in-del | -/T | 0.42 | 0.183303 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74701054 | ggccagcttgggctc[-/T]atTTTCTATTTTGTT | 18472 |
rs8239484 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74725256 | AATACTGTAAAAATC[A/G]CTTGGGAAGCTGCAG | 18472 |
rs8239485 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74725374 | AGTATAAAATAAACC[C/T]AGTAGCCAAACAAAG | 18472 |
rs8239486 | snp | G/T | 0.375 | 0.216506 | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74725475 | GCCTCAGGAGCATCC[G/T]TTTTATAAAAAACAA | 18472 |
rs8239487 | snp | A/T | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74723716 | GCTTGAACCCTCAGC[A/T]GCCTGAGTAGCCCAC | 18472 |
rs8239488 | snp | A/G | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Pafah1b1 | GRCm38.p3 | 11:74723404 | CCCCGGTGCGGTGGT[A/G]GTCCAGCCTCTGCAT | 18472 |
rs8239489 | snp | G/T | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Pafah1b1 | GRCm38.p3 | 11:74723378 | TGCATTCAGTAAAGA[G/T]CTGCAGCATCCACCC | 18472 |
rs8239492 | in-del | -/T | 0.375 | 0.216506 | intron-variant | Pafah1b1 | Mm_Celera | 11:74679686 | CACTAAAACCAGTCC[-/T]TTTTTTTCTTTTTTC | 18472 |
rs8239493 | snp | A/G | 0.188366 | 0.242283 | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | GRCm38.p3 | 11:74676896 | GAGTTGTATTCTCCA[A/G]ACTGTTGGACTGTGT | 18472 |
rs8254301 | snp | C/T | 0.165289 | 0.235211 | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74724591 | ATCCCTTGGGAAGCT[C/T]CCCTTTTGCTCTAAA | 18472 |
rs8254302 | snp | C/T | 0.152778 | 0.230321 | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74724706 | CACTGGCATTTCGGC[C/T]CCTGCTGGCTAGAGC | 18472 |
rs8254303 | snp | A/G | 0.152778 | 0.230321 | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74724842 | GGCAGAAGAGCTGTT[A/G]AGGTTAAAAGGCAGA | 18472 |
rs8254310 | snp | A/G | 0.496528 | 0.0415217 | utr-variant-5-prime, nc-transcript-variant | Pafah1b1 | GRCm38.p3 | 11:74699410 | TAATTCAAATCCAGG[A/G]ATCACAACTTTTGAT | 18472 |
rs8254311 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74699044 | CTCACTCTGTAGACC[C/T]GGCTGGCCTCGAACT | 18472 |
rs8254312 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74697909 | GTTGCTGGGATTTGA[A/G]CTCACGACCTTCAGA | 18472 |
rs8254313 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74697822 | TGTAGGGGATCTGAA[C/T]TCAGGTCCTAAGACT | 18472 |
rs8254314 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74697800 | CCTAAGACTTGGATG[A/G]CAAGCAGTTTTCTCA | 18472 |
rs8254315 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Pafah1b1 | Mm_Celera | 11:74697758 | ccctagcTTGTTTGT[C/T]TTAATCTAGGATGTT | 18472 |
rs8254316 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Pafah1b1 | Mm_Celera | 11:74697740 | AATCTAGGATGTTAT[A/T]AAAAAATAATCCTTT | 18472 |
rs8254317 | in-del | -/T | 0.142012 | 0.225474 | intron-variant | Pafah1b1 | Mm_Celera | 11:74697705 | TGCCATAGTGTCTCT[-/T]NATCGTTTATCAGTA | 18472 |
rs8254318 | in-del | -/T | 0.142012 | 0.225474 | intron-variant | Pafah1b1 | Mm_Celera | 11:74697704 | GCCATAGTGTCTCTN[-/T]ATCGTTTATCAGTAA | 18472 |
rs8254319 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74697681 | ATCAGTAAAGAATGG[C/T]TTAAGCGAAGAATCG | 18472 |
rs8254320 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74697658 | AAGAATCGTCATTGG[A/C]CATTAAATCTAGGGG | 18472 |
rs8254321 | snp | A/C | 0.486111 | 0.0821678 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74689720 | GTAAGACACATAGTG[A/C]TCTTTTTTCAGTTAC | 18472 |
rs8254322 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74682212 | TGCATAATCGTATTA[C/T]TTCTTTGGCATCTTC | 18472 |
rs8254323 | in-del | -/G | 0.32 | 0.24 | intron-variant | Pafah1b1 | Mm_Celera | 11:74682035 | AAACCAGTCAGTGCT[-/G]GGGGGTAGGGTCTTA | 18472 |
rs8254326 | snp | C/T | 0.110727 | 0.207612 | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | GRCm38.p3 | 11:74675029 | ATAGAATTGTGTACT[C/T]GGATGGTTGTTGATT | 18472 |
rs8254327 | snp | A/G | 0.110727 | 0.207612 | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | GRCm38.p3 | 11:74674906 | TGTAGACATGACCTG[A/G]AGAATAGTTGCTTTT | 18472 |
rs8254328 | snp | A/T | 0.49948 | 0.0161206 | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74674871 | TGACATCTTGCACTT[A/T]AGGAGACTAAGACCG | 18472 |
rs8254329 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74681977 | GGAGAAAGCTCTTAC[A/G]GACTTGTTTACTTTT | 18472 |
rs8254330 | in-del | -/T | 0.152778 | 0.230321 | intron-variant | Pafah1b1 | Mm_Celera | 11:74681885 | ctagatagagttaca[-/T]ncagactggtgtgag | 18472 |
rs8254331 | in-del | -/A | 0.152778 | 0.230321 | intron-variant | Pafah1b1 | Mm_Celera | 11:74681884 | tagatagagttacan[-/A]cagactggtgtgagt | 18472 |
rs13461650 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | Pafah1b1 | GRCm38.p3 | 11:74724178 | CTCGAGCCCCGGAAC[A/G]GCCGAGGAGCCCGCC | 18472 |
rs13461651 | snp | C/T | 0.336735 | 0.234472 | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74674482 | AAACCCAGTGTGTTG[C/T]TTAATCTAGATGGTG | 18472 |
rs13461652 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74674412 | ATTGCAAGAAAGGTT[C/T]TGGGTTTTTTCCAGT | 18472 |
rs16798119 | snp | A/G | 0.117188 | 0.211804 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74689754 | TAAGTTATAACTTCC[A/G]AGGcattggttctca | 18472 |
rs26904621 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pafah1b1 | Mm_Celera | 11:74716736 | AAAGCCTTATACCTG[C/T]AAAATATCCAATGCA | 18472 |
rs26904622 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Pafah1b1 | Mm_Celera | 11:74716701 | TTAGATATTGTCTGA[C/T]AACCCCTACTCAAAT | 18472 |
rs26904623 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Pafah1b1 | Mm_Celera | 11:74715760 | TCTGTGTTAAAAGCA[C/T]ATATATAAGGCCCTA | 18472 |
rs26904624 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Pafah1b1 | Mm_Celera | 11:74714512 | TACCTACTAGCTATA[C/T]AGAACATACAAATTA | 18472 |
rs26904625 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Pafah1b1 | Mm_Celera | 11:74713895 | TGTGGTTTAAGAATT[A/G]TCAAGGAGgccgggt | 18472 |
rs26904626 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Pafah1b1 | Mm_Celera | 11:74713887 | TTAAAAACTGTGGTT[C/T]AAGAATTATCAAGGA | 18472 |
rs26904627 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74713861 | AAAAAGAAAACGAGG[C/G]AGGAAAGGACTTAAA | 18472 |
rs26904628 | snp | A/T | 0.401235 | 0.199068 | intron-variant | Pafah1b1 | Mm_Celera | 11:74713099 | AGAATTTTGGAGTCA[A/T]GCAACAAAAGTTTAA | 18472 |
rs26904629 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Pafah1b1 | Mm_Celera | 11:74712923 | TTAAGTTAGTCCCAT[A/G]TTTTGTGTTGCTTAT | 18472 |
rs26904630 | snp | G/T | 0.495868 | 0.0452663 | intron-variant | Pafah1b1 | Mm_Celera | 11:74709397 | GTTTCTCTTATACTC[G/T]ACACCAAGCAGGATG | 18472 |
rs26904631 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Pafah1b1 | Mm_Celera | 11:74709374 | TTTATTTCTAGCAGT[C/T]TATCTGAGTTTCTCT | 18472 |
rs26904632 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Pafah1b1 | Mm_Celera | 11:74708694 | GATGTGAGCTAAATG[G/T]ATTTATTATGTCTTG | 18472 |
rs26904633 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Pafah1b1 | Mm_Celera | 11:74707727 | GTGGAGTAGGAAGGG[C/T]CTTTAAACAAGTCTG | 18472 |
rs26904634 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pafah1b1 | Mm_Celera | 11:74707057 | AACAGAAAACATCCA[C/T]GTAAGGGGCTGTGGA | 18472 |
rs26904635 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Pafah1b1 | Mm_Celera | 11:74707044 | CTTAGGCATGAACAA[C/T]AGAAAACATCCATGT | 18472 |
rs26904636 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74706840 | AGACAAACTCAACTA[A/G]AATGGTCTATAATTA | 18472 |
rs26904637 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74706665 | AAACCTTTTTTCTTT[C/T]AAAACACTGGCATGT | 18472 |
rs26904638 | snp | C/T | 0.32 | 0.24 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74706192 | TTTGTAATGTGGTCT[C/T]AGAAAGCAAATACAC | 18472 |
rs26904639 | snp | A/G | 0.32 | 0.24 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74706059 | CACTGCACTGGAATT[A/G]TATGCTATGATAGCT | 18472 |
rs26904640 | snp | G/T | 0.375 | 0.216506 | intron-variant | Pafah1b1 | Mm_Celera | 11:74705809 | ACAAATGTGATAGTG[G/T]TTTTTTTTTAAGATT | 18472 |
rs26904641 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Pafah1b1 | Mm_Celera | 11:74704936 | ATGGGACATACACTG[C/T]TTTCTAAAAATAATT | 18472 |
rs26904642 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Pafah1b1 | Mm_Celera | 11:74704243 | CTTGGCACACTGCTT[C/T]AAACACTCTGGAATA | 18472 |
rs26904643 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Pafah1b1 | Mm_Celera | 11:74704232 | GTACAGGCACGCTTG[A/G]CACACTGCTTTAAAC | 18472 |
rs26904644 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Pafah1b1 | Mm_Celera | 11:74704227 | TTCATGTACAGGCAC[A/G]CTTGGCACACTGCTT | 18472 |
rs26904645 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Pafah1b1 | Mm_Celera | 11:74703207 | TGGAATACGCACTCT[C/T]ATATTGCTTAACTTT | 18472 |
rs26904646 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Pafah1b1 | Mm_Celera | 11:74702450 | CTGGGTTTTTTCCCT[C/G]CACCAAGAATCACTT | 18472 |
rs26904647 | snp | A/C | 0.35503 | 0.226867 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74701231 | CTGCCAGTTAAGATG[A/C]CTAAACATTGATGTG | 18472 |
rs26904648 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Pafah1b1 | Mm_Celera | 11:74700529 | GAGAGGAAGAAAGGC[A/G]AACTGTGTCTAGTAT | 18472 |
rs26904649 | snp | G/T | 0.484429 | 0.0868505 | intron-variant | Pafah1b1 | Mm_Celera | 11:74699789 | TCCTGGCCCCGTAAG[G/T]GTTTCAGACATAGGT | 18472 |
rs26904650 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Pafah1b1 | Mm_Celera | 11:74699248 | TTGTCTTTACCACCC[A/T]AAGCCTAGTTAATCA | 18472 |
rs26904651 | snp | A/C | 0.304688 | 0.243945 | intron-variant | Pafah1b1 | Mm_Celera | 11:74698701 | TCACTTTGCTTTAAA[A/C]TCAAACATGACAAAT | 18472 |
rs26904652 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Pafah1b1 | Mm_Celera | 11:74698519 | TCACGCCCTGCTCAT[A/G]TCTCTGTTTCTTGAA | 18472 |
rs26904653 | snp | C/G | 0.415225 | 0.187619 | intron-variant | Pafah1b1 | Mm_Celera | 11:74693468 | GTCCAATGTGGCAGG[C/G]CCTATGAAATCTAAC | 18472 |
rs26904654 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74689275 | TGACTATGAAGCTTA[C/T]GGTAGTCCAGAACTT | 18472 |
rs26904655 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Pafah1b1 | Mm_Celera | 11:74685560 | TAGATACTGCAGCAC[C/T]GAACTCTGGCTTCTA | 18472 |
rs26904656 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74682592 | TCCTAGCATGAAAAA[A/G]GGCCCTGATCAATAT | 18472 |
rs26904657 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Pafah1b1 | Mm_Celera | 11:74679382 | CTTACCTGGAAAAGT[C/T]GACAAGGTTACATAA | 18472 |
rs26904658 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Pafah1b1 | Mm_Celera | 11:74678789 | AGCTTCACTAGCTGG[C/T]ATACCACTGAAcaac | 18472 |
rs26904659 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Pafah1b1 | Mm_Celera | 11:74678738 | TCACTAGCTGGTATA[C/G]TGCAGTATCAGGGAT | 18472 |
rs26904660 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Pafah1b1 | Mm_Celera | 11:74677995 | ACTGGATTAGGAATG[C/T]TGAAACTCAATTATT | 18472 |
rs26904661 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Pafah1b1 | Mm_Celera | 11:74677913 | CTGCCTCCACACTTG[A/G]ATACAATGTCCACGA | 18472 |
rs26904662 | snp | C/T | 0.33241 | 0.236027 | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | GRCm38.p3 | 11:74677539 | GTAACATTTAATAAG[C/T]TCAATCTACATCCAG | 18472 |
rs26904663 | snp | A/G | 0.244898 | 0.249948 | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | GRCm38.p3 | 11:74677072 | CACTAGCCTTTGCTT[A/G]ATAGGCTGCCAAAAC | 18472 |
rs26904664 | snp | A/G | 0.260355 | 0.249785 | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74676532 | CAACATGGAGGTTAT[A/G]TGTGTGTGATATACA | 18472 |
rs26904665 | snp | C/T | 0.401235 | 0.199068 | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | GRCm38.p3 | 11:74676342 | AGCCTATGAGGAATG[C/T]GTAACATGGTGACTG | 18472 |
rs26904666 | snp | A/G | 0.487535 | 0.077957 | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74676308 | AAACCTACTGTAGAA[A/G]CTCTGGATCAAAATA | 18472 |
rs26904667 | snp | A/G | 0.132653 | 0.220748 | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74674960 | CTCCATGCGGTTAGG[A/G]CTTCTTGGGCACGCT | 18472 |
rs26904668 | snp | A/G | 0.489796 | 0.070696 | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74674792 | GGACGGCTTGCTAAT[A/G]CTAGTGATTGTGGGT | 18472 |
rs26904669 | snp | A/C | 0.489796 | 0.070696 | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74674769 | GACTAATAGTGCATC[A/C]CGGCCCGGGACGGCT | 18472 |
rs26904670 | snp | A/C | 0.132653 | 0.220748 | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74674745 | AGCCTAAAGCCAAAG[A/C]TTCCAAAGGACTAAT | 18472 |
rs26904671 | snp | A/G | 0.132653 | 0.220748 | downstream-variant-500B | Pafah1b1 | Mm_Celera | 11:74673724 | GCTTAGCTGTGCAGT[A/G]CAGTCAGTAGTTCTA | 18472 |
rs29384699 | snp | C/T | 0.5 | 0 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74719583 | TATGCAAGCTAACTT[C/T]TTAAGTTTTGGGGCA | 18472 |
rs29385169 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74718454 | TATCCCAGCAACCAC[A/G]TGGTCGCTCACAACC | 18472 |
rs29385937 | snp | C/T | 0.5 | 0 | intron-variant | Pafah1b1 | Mm_Celera | 11:74713347 | GTAAGCATCACCCCT[C/T]CATGACCTCTGCATC | 18472 |
rs29389927 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74722282 | TTTTGCGAAAAAACT[G/T]GTTTCCTTTCTGACT | 18472 |
rs29393735 | snp | C/T | 0.32 | 0.24 | intron-variant | Pafah1b1 | Mm_Celera | 11:74697138 | TCCTTTTTTTTTTTT[C/T]CCCCCCCCCGGGACA | 18472 |
rs29394188 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Pafah1b1 | Mm_Celera | 11:74704148 | AGGTCACATTTTTTT[A/T]TAATTTACTTTAGTG | 18472 |
rs29394326 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74718402 | AGATGGCTCAGTGGT[G/T]AAGAGCACTAACTGC | 18472 |
rs29394869 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74703589 | TTAGCTAGGTACCCT[A/G]GTACATACATTCCCT | 18472 |
rs29395535 | snp | C/T | 0.5 | 0 | intron-variant | Pafah1b1 | Mm_Celera | 11:74680126 | TGTGCCTGTACGACA[C/T]GTTGAATGCAGTGCT | 18472 |
rs29396397 | snp | C/T | 0.5 | 0 | intron-variant | Pafah1b1 | Mm_Celera | 11:74692899 | CATAGGCAATCACTA[C/T]TGTGACTTACATGTT | 18472 |
rs29397814 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74716376 | TAAGGGCTGGAGAGA[C/T]GGCTCAGTGCTAAGA | 18472 |
rs29399234 | snp | A/C | 0.5 | 0 | intron-variant | Pafah1b1 | Mm_Celera | 11:74711104 | TTGTTATATATATAT[A/C]TGACTAGTTAATTAT | 18472 |
rs29402612 | snp | C/T | 0.5 | 0 | intron-variant | Pafah1b1 | Mm_Celera | 11:74685256 | GGCTTGTTTTAAAAT[C/T]GCTAACACAGCATTT | 18472 |
rs29402882 | snp | G/T | 0.5 | 0 | intron-variant | Pafah1b1 | Mm_Celera | 11:74679024 | AAGAGCACTGACTGC[G/T]CTTCTGAAGGTCCTC | 18472 |
rs29403274 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74694100 | AATGGGGGTAGGGTG[A/G]GGTAAAGAGAGGACC | 18472 |
rs29405142 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Pafah1b1 | Mm_Celera | 11:74697252 | CTCTGCCTCCCAAGT[A/G]CTGTTTTCCAAGACA | 18472 |
rs29405584 | snp | C/T | 0.5 | 0 | intron-variant | Pafah1b1 | Mm_Celera | 11:74711199 | GATGATTGCATGGGG[C/T]TGGCATGACAATGGC | 18472 |
rs29406899 | snp | A/T | 0.5 | 0 | intron-variant | Pafah1b1 | Mm_Celera | 11:74698257 | TTAAGTAATTACTCT[A/T]CTGTTCTGCTTTTTT | 18472 |
rs29406907 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Pafah1b1 | Mm_Celera | 11:74704147 | AAGGTCACATTTTTT[A/T]TTAATTTACTTTAGT | 18472 |
rs29407643 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74691434 | CCACTGAGCCATCTC[A/G]CCAGCCCTCTAGATA | 18472 |
rs29409639 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74712534 | TTCCCAACAACCATA[C/T]CATAGAGCTCACAAC | 18472 |
rs29410624 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Pafah1b1 | Mm_Celera | 11:74704149 | GGTCACATTTTTTTT[A/T]AATTTACTTTAGTGT | 18472 |
rs29412348 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74691223 | GATTAAAGGCGTGCG[C/T]CACCACTGCCCAGCT | 18472 |
rs29413818 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74684304 | TGTTTGTCAGTCATA[A/G]TGATCATTCTAGATT | 18472 |
rs29414134 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74707119 | CTTCCAGAAAACTCA[A/G]TTGTATTTCCCAGCA | 18472 |
rs29414164 | snp | G/T | 0.5 | 0 | intron-variant | Pafah1b1 | Mm_Celera | 11:74700441 | AATAAAATTAGATCT[G/T]TAGATTTAACATAGT | 18472 |
rs29415899 | snp | C/T | 0.5 | 0 | intron-variant | Pafah1b1 | Mm_Celera | 11:74705075 | TATTTTAATTTTATT[C/T]AACAGATAAAACGTA | 18472 |
rs29416541 | snp | A/C | 0.5 | 0 | intron-variant | Pafah1b1 | Mm_Celera | 11:74692626 | GCCACCCTGCCATAT[A/C]TCTGAGCGTTGGGAT | 18472 |
rs29416690 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74702988 | AATGCAAATCCTGCC[A/C]GTTATAGTTACTGTA | 18472 |
rs29417165 | snp | A/G | 0.5 | 0 | intron-variant | Pafah1b1 | Mm_Celera | 11:74709257 | TGAACTGGGCTACAC[A/G]GCAAAACAAATCACC | 18472 |
rs29418847 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74711989 | CTTGACCACCTTATC[C/T]CTAATCTCAGGACTC | 18472 |
rs29422624 | snp | C/T | 0.5 | 0 | intron-variant | Pafah1b1 | Mm_Celera | 11:74681288 | ATGTGCTGCTGCTGC[C/T]ACCACCACTTCCGAC | 18472 |
rs29423457 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74719622 | AAACAAACAAACAAA[A/C]AAAAAAAAAAAACCC | 18472 |
rs29428400 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74720635 | TTCATAATATGGATA[A/T]TTTATTCAGAAAGTT | 18472 |
rs29428471 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74718459 | CAGCAACCACGTGGT[C/G]GCTCACAACCATCTA | 18472 |
rs29428721 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74700826 | TGCATGTGTGAGTAT[A/G]TAAGAATATATGGGC | 18472 |
rs29429447 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Pafah1b1 | Mm_Celera | 11:74699936 | CCTGGTTGCCTAACA[C/T]GCTTAACAATCCTCC | 18472 |
rs29430817 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Pafah1b1 | Mm_Celera | 11:74686933 | AATTTTTAAAAATAA[C/T]GATTTTTGCACTTGT | 18472 |
rs29431507 | snp | A/T | 0.5 | 0 | intron-variant | Pafah1b1 | Mm_Celera | 11:74706885 | AAATTAAACCCAAAT[A/T]GATTATTGTTGGTGA | 18472 |
rs29431988 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74719616 | AAACAAAACAAACAA[A/C]CAAAAAAAAAAAAAA | 18472 |
rs29433015 | snp | C/G | 0.5 | 0 | intron-variant | Pafah1b1 | Mm_Celera | 11:74679953 | TATATACTACCATGT[C/G]TGATCTTGTGCCATG | 18472 |
rs29434753 | snp | A/T | 0.5 | 0 | intron-variant | Pafah1b1 | Mm_Celera | 11:74685312 | TATTCCATCATCTTT[A/T]AAGAAAACAGAGCCA | 18472 |
rs29435966 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74690988 | ATATAAATATTTCTG[A/G]AAATAAGATGGACAC | 18472 |
rs29436710 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74699004 | TAATCCCAGCATTTG[A/G]GAGACAGAGGCAGGC | 18472 |
rs29439948 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pafah1b1 | Mm_Celera | 11:74679671 | TAGAACACATTTTAA[C/T]ACTAAAACCAGTCCT | 18472 |
rs29440398 | snp | C/T | 0.5 | 0 | intron-variant | Pafah1b1 | Mm_Celera | 11:74680128 | TGCCTGTACGACATG[C/T]TGAATGCAGTGCTCT | 18472 |
rs29440779 | snp | A/G | 0.5 | 0 | intron-variant | Pafah1b1 | Mm_Celera | 11:74680826 | ACAGGCCAGACAGGA[A/G]TATGTCATAAAACCC | 18472 |
rs29441528 | snp | A/G | 0.32 | 0.24 | intron-variant | Pafah1b1 | Mm_Celera | 11:74683820 | AAAAGAAAAGTAAAA[A/G]TAATAAAAAATGGGC | 18472 |
rs29442003 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74722272 | TGCACAAATATTTTG[C/T]GAAAAAACTGGTTTC | 18472 |
rs29442184 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74711281 | CAGAGAGTGCTGAGA[C/T]GAGAACGCCCTGCTG | 18472 |
rs29442253 | snp | A/T | 0.5 | 0 | intron-variant | Pafah1b1 | Mm_Celera | 11:74687389 | TTAATCCCAGGACTC[A/T]GGAGTCAGAGGTAGG | 18472 |
rs29443894 | snp | C/T | 0.5 | 0 | intron-variant | Pafah1b1 | Mm_Celera | 11:74694243 | CATAAGACAAAATAC[C/T]TATACACATATTAAA | 18472 |
rs29444658 | snp | A/G | 0.5 | 0 | intron-variant | Pafah1b1 | Mm_Celera | 11:74694142 | CTCAGCACCTACATG[A/G]TAACACACAATTTGT | 18472 |
rs29444929 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74720709 | GTATGTTGACACACA[C/T]CTGCTTTACAGCACT | 18472 |
rs29450859 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74723118 | TAAAGCCAGGCACCT[C/T]GCTTTCTCCTATCTC | 18472 |
rs29450921 | snp | C/T | 0.5 | 0 | intron-variant | Pafah1b1 | Mm_Celera | 11:74693140 | GAGCTCACTATGAAG[C/T]TTAGAGTTACCCAGT | 18472 |
rs29453236 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74720397 | TTTTTACCATTATGT[G/T]TATGTGTCAGTCAGA | 18472 |
rs29454811 | snp | G/T | 0.5 | 0 | intron-variant | Pafah1b1 | Mm_Celera | 11:74687606 | TATAAAAACTATAAG[G/T]AAATTCTAGTATGTA | 18472 |
rs29455248 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74725558 | TAACACTGAGGAGAC[G/T]GAGGCAGGAGACTTG | 18472 |
rs29456632 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74706982 | CCAGCCTGGGATATA[G/T]AAACCTTTAAAAAAC | 18472 |
rs29457469 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74724850 | AGCTGTTGAGGTTAA[A/G]AGGCAGATGGATTGC | 18472 |
rs29461717 | snp | C/T | 0.5 | 0 | intron-variant | Pafah1b1 | Mm_Celera | 11:74691189 | TAAGTTTCTCACTTA[C/T]TTTAATCCCGAGTGC | 18472 |
rs29462474 | snp | A/G | 0.5 | 0 | intron-variant | Pafah1b1 | Mm_Celera | 11:74694840 | TCTGTTTTATCAGTG[A/G]TAGTTTTGTTTCTGA | 18472 |
rs29465861 | snp | A/G | 0.5 | 0 | intron-variant | Pafah1b1 | Mm_Celera | 11:74681286 | GTATGTGCTGCTGCT[A/G]CTACCACCACTTCCG | 18472 |
rs29466935 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74686638 | CACACCCAGCTTTAA[A/G]AAGTCTCATTCTTAG | 18472 |
rs29468828 | snp | C/T | 0.375 | 0.216506 | intron-variant | Pafah1b1 | Mm_Celera | 11:74681311 | CTTCCGACTGGGCGG[C/T]CCTTCTTTTATCTTT | 18472 |
rs29469803 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Pafah1b1 | Mm_Celera | 11:74696985 | ACTGAGCCATCCTTC[C/T]AGCCCCTATCAGTGA | 18472 |
rs29469848 | snp | A/C | 0.375 | 0.216506 | intron-variant | Pafah1b1 | Mm_Celera | 11:74698187 | CTATGCAACCCCCCC[A/C]CACACACATGCACAC | 18472 |
rs29472505 | snp | C/T | 0.5 | 0 | intron-variant | Pafah1b1 | Mm_Celera | 11:74693018 | AAAGTCCTTGTTGGC[C/T]TGGAACAACTCATTT | 18472 |
rs29472925 | snp | A/G | 0.375 | 0.216506 | intron-variant | Pafah1b1 | Mm_Celera | 11:74686848 | ATTATGAATTAACAT[A/G]AATGAATATTACAGA | 18472 |
rs29473536 | snp | C/T | 0.5 | 0 | intron-variant | Pafah1b1 | Mm_Celera | 11:74697532 | CTTACCCCCTTTTTC[C/T]TTTTTAATAAAAGAC | 18472 |
rs29473638 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74691354 | GTTACAGATGGTTGT[A/G]AGCCACCATGTGGTT | 18472 |
rs29475579 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74712586 | GACAGTTCCTACTCC[A/G]GCCTCTGTGGACTCC | 18472 |
rs29476444 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74691711 | GTGTCCTATGTCAAG[A/T]CTGTACATCATTTAG | 18472 |
rs29476448 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Pafah1b1 | Mm_Celera | 11:74697140 | CTTTTTTTTTTTTTC[C/T]CCCCCCCGGGACAGG | 18472 |
rs29477562 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74720784 | AGGATACATAAGGAG[A/T]GAGAATTAAGCCAGG | 18472 |
rs29478060 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74718412 | GTGGTTAAGAGCACT[A/G]ACTGCTCTTTGGAGG | 18472 |
rs29478298 | snp | C/T | 0.5 | 0 | intron-variant | Pafah1b1 | Mm_Celera | 11:74687374 | TGGTGGTTCATGCCT[C/T]TAATCCCAGGACTCA | 18472 |
rs29480477 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Pafah1b1 | Mm_Celera | 11:74700726 | TGAGTTCAATTCCCA[C/T]CAACCACATGGTGGC | 18472 |
rs29481474 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Pafah1b1 | Mm_Celera | 11:74699937 | CTGGTTGCCTAACAT[G/T]CTTAACAATCCTCCT | 18472 |
rs29482837 | snp | A/C | 0.32 | 0.24 | intron-variant | Pafah1b1 | Mm_Celera | 11:74681196 | TTGTTCTTGTTTTTC[A/C]AGACAGGGTCATGCT | 18472 |
rs29487095 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Pafah1b1 | Mm_Celera | 11:74697139 | CCTTTTTTTTTTTTT[C/T]CCCCCCCCGGGACAG | 18472 |
rs29487245 | snp | C/T | 0.5 | 0 | intron-variant | Pafah1b1 | Mm_Celera | 11:74711037 | GGCAGCTTGTATCAT[C/T]ATCAATTGGCCCTGA | 18472 |
rs45786968 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74715237 | ACAAACCAAAAAAAA[A/C]AAAAAAAAAAGAAAA | 18472 |
rs45865816 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74719905 | GTTTGAACTTTGAGA[C/T]TCAAGAGTGGAAAGA | 18472 |
rs45988702 | snp | A/C | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74688516 | TTTGCTATATAGCTG[A/C]TAATGAACTTGAATT | 18472 |
rs46154531 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74713910 | ATCAAGGAGGCCGGG[C/T]GTGGTGGAGCACGCC | 18472 |
rs46176079 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74710687 | TCTGGAAGAGCTATC[A/G]GTGCTCTTAACCACT | 18472 |
rs46193316 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74707999 | TCTCTCTCTCCCCCT[C/T]CCTGTCTCCCCCACA | 18472 |
rs46300141 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74710744 | TTTTTAGTTATACAA[A/G]GCCAAAAAAAATATA | 18472 |
rs46331650 | snp | C/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74690071 | TGAACTTAAAACCAA[C/T]GTTTTCATGAAGCAA | 18472 |
rs46439691 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74707603 | TGGTTCTGTAAAACA[A/G]AATTAACGAAGTGAA | 18472 |
rs46650046 | snp | A/C | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74688391 | CTACATGAAAGCGAT[A/C]ACTGTGTGTTTAATT | 18472 |
rs47268301 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74683929 | CAAGTCTAATAAATG[C/T]ATACCAGCAGCATAT | 18472 |
rs47282861 | snp | A/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74689213 | TGAAGTTAAACAAAG[A/T]TGTGTTTTATAATAT | 18472 |
rs47326007 | snp | A/C | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74688619 | AAAAGGGCATCAGAT[A/C]CCATTACAGATATAG | 18472 |
rs47463360 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74682830 | GGAGTTCAAGGCCAG[C/T]CAGGTCTACATAGAG | 18472 |
rs47604951 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74683906 | AACACAATAAAACTT[A/T]AAAACCTCAAGTCTA | 18472 |
rs47974024 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74685147 | GAGACCGGTGTACTA[G/T]GCAGCCCAGTTGAGC | 18472 |
rs47979103 | snp | A/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74707842 | CACTTTCTACCTTAT[A/T]TTTTTTTTATATTTT | 18472 |
rs48160877 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74721167 | GGGGCAGAGGCAGGC[A/G]GATTTCTGAGTTCCA | 18472 |
rs48372236 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74713831 | ACATACATAAAATTT[A/T]AAAAAAGAAAAAAAA | 18472 |
rs48459809 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74710700 | TCAGTGCTCTTAACC[A/C]CTGAGCCATCTATCC | 18472 |
rs48630850 | snp | C/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74684700 | CTTTGATGATGATCA[C/T]AGGAGAAAATGCATT | 18472 |
rs48711336 | snp | C/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74689208 | GAACATGAAGTTAAA[C/T]AAAGTTGTGTTTTAT | 18472 |
rs49128383 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74711780 | TGGCCCACAACCATC[C/T]GTAACAAGACCTGAT | 18472 |
rs49604406 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74711689 | TAAAATACTCAGGCT[A/G]GAACAATGGCTCAGT | 18472 |
rs50169612 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74708177 | TGCCTCCCGAGTGCT[G/T]CGATTAAAGGTGTGC | 18472 |
rs50371923 | snp | A/G | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74684657 | AAGAGATAAGAGGCA[A/G]ATTTTGATCCTCTAT | 18472 |
rs50388683 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74710745 | TTTTAGTTATACAAA[A/G]CCAAAAAAAATATAT | 18472 |
rs50416666 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74717634 | TCCCAAGTGACTTCA[A/G]GAGAAGAAATTTGTA | 18472 |
rs50452032 | snp | C/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74708178 | GCCTCCCGAGTGCTT[C/G]GATTAAAGGTGTGCG | 18472 |
rs50545953 | snp | A/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74684659 | GAGATAAGAGGCAAA[A/T]TTTGATCCTCTATTT | 18472 |
rs50584816 | snp | C/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74713942 | TTAATCCCAGCACTC[C/G]GGAGACAGGCAGATT | 18472 |
rs50664834 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74685182 | ATTTGCCTTAAACCT[A/G]TGATCCTCCCACAAA | 18472 |
rs50808772 | snp | G/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74713857 | AAAAAAAAAGAAAAC[G/T]AGGGAGGAAAGGACT | 18472 |
rs50959925 | snp | C/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74706670 | TTTTTTCTTTCAAAA[C/G]ACTGGCATGTATCAG | 18472 |
rs51025400 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74711553 | AAACATTTTAATTAA[C/T]CTAAGGATGAATTCT | 18472 |
rs51106398 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74719950 | GTACCCTGACCTAAT[C/T]CACACAAAGAACACA | 18472 |
rs51188324 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74683878 | TAAAATAAGCTGACA[A/G]GAAACACCACTAAAC | 18472 |
rs51224946 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74711769 | CAACCACATGGTGGC[C/T]CACAACCATCCGTAA | 18472 |
rs51268833 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74698459 | TCAAACTCAGAAATC[C/T]GCCTGCCTCTGCCTC | 18472 |
rs51518768 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74683157 | CTTGCCATGGCATGC[A/T]GACAGACATCAAAGG | 18472 |
rs51642020 | snp | C/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74690751 | CCCTGGAACTCACTA[C/T]GTAAACCAGGCTAAC | 18472 |
rs51686053 | snp | C/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74689353 | CTGGAACTAATCCAC[C/T]CAGACAACTTTCATT | 18472 |
rs51689073 | snp | C/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74689440 | TTTTTAGAGTTTTTT[C/T]CCCTATACCACAGTT | 18472 |
rs51825966 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74706598 | AGGATCCCCTTGCCT[C/T]TGCGCCCCTTCCCCC | 18472 |
rs52019237 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74713922 | GGGTGTGGTGGAGCA[C/T]GCCTTTAATCCCAGC | 18472 |
rs52194490 | snp | C/G | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74707275 | ACACACACACAGACA[C/G]ACACACACACACAGA | 18472 |
rs52208416 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74684109 | CACAGTGCATACAGT[A/G]CAGTGTGTGTATGAA | 18472 |
rs52238181 | snp | A/G/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74684123 | TGCAGtgtgtgtatg[A/G/T]atggatggatgaatg | 18472 |
rs52257690 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74694342 | TCAAAAGTAAAAAAA[A/T]TTTTAAAAAAGGAAG | 18472 |
rs52263295 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74719789 | GGCTTGGACCTCACA[A/G]AGATCCACCTCTGCC | 18472 |
rs52275851 | snp | A/C | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74688925 | AAAACAAAAACCAAA[A/C]AAACAAAAACCACAA | 18472 |
rs52297710 | snp | A/G/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74684135 | ATGAATGGATGGATG[A/G/T]ATGTATGTATGTATG | 18472 |
rs52333306 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74710542 | TTTTTTAAACTCAGG[A/G]TTTTTTTTTTTTTTT | 18472 |
rs52404851 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74694347 | AGTAAAAAAATTTTT[A/T]AAAAAGGAAGTTTAA | 18472 |
rs52429688 | snp | A/G | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74695536 | CACGCACACGCGCAC[A/G]CACACACACACAGAG | 18472 |
rs107664968 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74713283 | AGAACCCAAGACTAC[C/T]AGCCCAGGGATGGCA | 18472 |
rs107720171 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74708046 | GAAGGTTTTGTTTTT[G/T]GTTTTGTTTTTTTGT | 18472 |
rs107824946 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74695554 | CACACACACAGAGTA[C/T]GTAGCATACACACAG | 18472 |
rs108158912 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74693162 | TTACCCAGTACTTAT[A/G]ATCCTGTCCCAGCCT | 18472 |
rs108383873 | snp | A/C | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74701280 | AAACAACAACAACAA[A/C]AAAATTATAAAGAAT | 18472 |
rs108448602 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74708040 | GGGGGGGAAGGTTTT[G/T]TTTTTGGTTTTGTTT | 18472 |
rs108594230 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74713260 | GGATGGCACCACCCA[A/C]AATGGGTTAGATCCT | 18472 |
rs211770628 | in-del | -/A | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74695710 | AATGGATGACTGGTT[-/A]AAAAAAAACAAAAGC | 18472 |
rs211808984 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74686452 | AAATCATAAACTATA[A/C]ACTATCCCTGAATCA | 18472 |
rs211826945 | in-del | -/GGGCCT | | | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74724454 | GCGCATGCGCGGGCC[-/GGGCCT]GGGCCTGGGCCTGGG | 18472 |
rs211829538 | in-del | -/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74709746 | AAACTTTTTTTTTAG[-/T]TTTTTTTTATAATTC | 18472 |
rs211875075 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74687468 | CCAAGACAGCCAGGG[C/T]TTGTTACAGAGAAAC | 18472 |
rs211979129 | in-del | -/GA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74714033 | AGAAACCCCGTCTCG[-/GA]AAAAAAAAAAAAAAA | 18472 |
rs212009209 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74675883 | TTGTCCTCAAAAATA[A/G]CCACTTAATTCTCAA | 18472 |
rs212179353 | snp | A/G | | | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74724632 | GCTGGCGTCCATCAC[A/G]ACTCTTGCTCTGCCT | 18472 |
rs212305510 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74713615 | TAATCTGATCTTTTT[A/G]AATCAATTAGTCATT | 18472 |
rs212374746 | snp | A/G | | | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74726051 | CATGTAACCATTACT[A/G]TCTAGTACCAAAGCC | 18472 |
rs212380037 | in-del | -/AAAAAG | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74715496 | TCTCGAAAAACCAAA[-/AAAAAG]AAAAAGAAAAAGAAA | 18472 |
rs212443401 | in-del | -/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74687161 | ACACACACACACACA[-/C]ACAAAAATTTGGAGA | 18472 |
rs212575413 | in-del | -/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74699228 | CTGAAGATGATGGAT[-/G]GGGCTTGTCTTTACC | 18472 |
rs212645574 | in-del | -/A | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74708403 | CCTCAACTGGTTTCT[-/A]ACTATTATCCACACT | 18472 |
rs212768042 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74684620 | ATCTAAATGACAAGA[C/T]CATTAAAAGTAGTAA | 18472 |
rs212788193 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74712301 | GGAGGCATGTAGCTA[A/G]GAAGAAACAAGACAG | 18472 |
rs212789139 | in-del | -/A | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74717478 | TTGTTTTGATCATAG[-/A]CCCTTAATATTTGTG | 18472 |
rs212790121 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74721861 | TAATTAAAAAAAAAA[A/C]ACTAGCCAGAGCATA | 18472 |
rs212856145 | snp | C/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74702199 | acacacacacacaca[C/T]AAAGTTCTTACCACC | 18472 |
rs212870725 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74708419 | ACTATTATCCACACT[A/T]ATGTTTGTCTCCATT | 18472 |
rs212903785 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74682994 | ATTAATATGTAGGGG[G/T]TTTTATGGAGGAGGG | 18472 |
rs212948601 | snp | C/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74680157 | CTCAGCAGCCCAAGA[C/G]GGGATTGGATCCCCT | 18472 |
rs213028282 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74692733 | ACTACTTAAGTAGGA[C/T]GGTCGTACCTTGAAC | 18472 |
rs213082912 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74707607 | TCTGTAAAACAAAAT[A/T]AACGAAGTGAACCAT | 18472 |
rs213424698 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74724248 | AGCGCTCCCCTCCGG[C/G]TCCTCCTCGCTCCCT | 18472 |
rs213424778 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74708835 | AACAGAACTGTTGTT[A/C]TAACTGACCATGTCA | 18472 |
rs213483098 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74710539 | TTTTTTTTTAAACTC[A/T]GGGTTTTTTTTTTTT | 18472 |
rs213495847 | in-del | -/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74697108 | CATATATACCAAGAA[-/T]TTTTTTGTTTGTTTT | 18472 |
rs213496176 | in-del | -/TTTATTTTAT | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74710563 | TTTTTTTTTTCTAGA[-/TTTATTTTAT]TTTATGTACATGAGT | 18472 |
rs213559137 | snp | C/G | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74701784 | ttaagaaaagaatat[C/G]ttcactagctgaagt | 18472 |
rs213626664 | in-del | -/A | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74690947 | ACCCTGTCTTGAACC[-/A]CCCCCCCAAAAAAGA | 18472 |
rs213647238 | in-del | -/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74717532 | CTAAGTATTTGTAAA[-/T]TTTTTTTTTCAAAAG | 18472 |
rs213653352 | snp | C/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74709519 | GGGGTACACAGTGAG[C/G]AGGATTATACCAATT | 18472 |
rs213697769 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74698537 | TCTGTTTCTTGAATT[C/T]TAGGATTAAAGATCT | 18472 |
rs213722239 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74682653 | TTAAACCAATCAGTA[C/T]TTTTTATATAAATTT | 18472 |
rs213766200 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74685600 | TTGCCTGCTCTCTTG[A/G]TAAATAAAATAAAAA | 18472 |
rs213798530 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74680361 | GATGACTGAGCAATT[A/T]AGAGCATTTTAGGGA | 18472 |
rs213819223 | in-del | -/AAAAAA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74683990 | TAAGAAAAACAAAAC[-/AAAAAA]AAAATAACAACAACA | 18472 |
rs213854482 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74681428 | AATTTCTCCTCCCAT[C/T]TCCCCACTGTACTCT | 18472 |
rs214071513 | in-del | -/TT | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74718737 | TTTTCTTGAAATGCC[-/TT]TTTTTTTTTTTGAGG | 18472 |
rs214108571 | snp | C/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74717776 | CAAATTCAGTAGCGA[C/G]AAGCTAGACAATGTT | 18472 |
rs214182771 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74706938 | aggtagaaagcagag[G/T]catccttagctacag | 18472 |
rs214267535 | in-del | -/CGC | | | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74724385 | GCCCTGACGTCACCG[-/CGC]CGCCGCCGCCGCCCC | 18472 |
rs214361871 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74719419 | AAATACTTTTATAAC[A/G]GACTTCTATTAGAAG | 18472 |
rs214374839 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74695011 | TTCCTTACAGAAGCC[A/G]GTCGATGGTGGCGCA | 18472 |
rs214424219 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74720361 | GCATATAATCTAAGA[A/G]CCAGCAACATTTACT | 18472 |
rs214449733 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74687163 | ACACACACACACACA[A/C]AAAAATTTGGAGAAA | 18472 |
rs214508110 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74713708 | TTGATCTCCAGCAAG[C/T]CACAAATTTTCTTAA | 18472 |
rs214551240 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74715257 | AAAAAAGAAAACCCA[A/T]CCATCTGTCATAAAT | 18472 |
rs214612144 | snp | C/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74716516 | GCCACAGTGTACTTA[C/G]ATATAATAATAAATA | 18472 |
rs214639374 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74694178 | AAAAACCTGACAACC[C/T]TTCTGATAATCTATA | 18472 |
rs214671371 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74678828 | CACTTAAGCCTTTAA[C/T]ACATCCTCATGGTGT | 18472 |
rs214727809 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74681758 | aacaaagagatgata[A/G]ctgaaaagagaagaa | 18472 |
rs214764314 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74717979 | caaaaAACAAAAAAC[A/T]ATTGAGAGAATTTCT | 18472 |
rs214812269 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74678087 | TATTCACCCAGCATA[C/T]TGATTTACTGAATGT | 18472 |
rs214857156 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74704040 | ATAGACAGCTCCTCA[G/T]CCCAGAAAATAAAAC | 18472 |
rs214888939 | in-del | -/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74679199 | AATAGGAAAGAAAAA[-/T]TACCAGCCAGTCAAT | 18472 |
rs214904434 | in-del | -/TATTC | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74693926 | GAGGGAAACACGTGA[-/TATTC]TATTCTATTCTATTC | 18472 |
rs214932846 | in-del | -/A | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74682437 | TACTTGAAATCTTGC[-/A]AAAAAAAAGCTGTTT | 18472 |
rs215003440 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74707706 | AGTTGAAGGGTGTTT[A/G]TATCAGTGGAGTAGG | 18472 |
rs215145834 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74707796 | CTGTATGTTACTGCA[A/G]GAGGCTGGGGCTGAC | 18472 |
rs215201206 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74695149 | CCCTGTCTCGAAAAA[A/C]CAAAAAAAATAAGTT | 18472 |
rs215205053 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74708188 | TGCTTCGATTAAAGG[C/T]GTGCGCCACCACGCC | 18472 |
rs215245378 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74719468 | AGGGCTAGTTCAGTG[A/T]TGGGTAACACCCAAG | 18472 |
rs215332526 | snp | A/G | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74717657 | AATTTGTAGAATTTT[A/G]AATCTCAAAGTTCAA | 18472 |
rs215371663 | in-del | -/G | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74715248 | AAAAAAAAAAAAAAA[-/G]AAAACCCAACCATCT | 18472 |
rs215541909 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74681533 | TCTCATCAGCACTTA[C/T]GTAGTTTCTAAAACT | 18472 |
rs215689525 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74692263 | TTAGAATGACATTTA[A/G]AATTATACTTTAAAG | 18472 |
rs215789745 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74720516 | ACCATCTCACCAGCC[C/T]CACTTTCCTTTTCTT | 18472 |
rs215832601 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74692420 | CACAGTTATAGAAAA[A/G]GTTGATTTAGGATTC | 18472 |
rs215981016 | in-del | -/CACACAC | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74687153 | ACACACACACACACA[-/CACACAC]ACACAAAAATTTGGA | 18472 |
rs216087859 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74716968 | ATAGAGAGACCTTGT[A/C]TTGAAAAACAAATCA | 18472 |
rs216131215 | in-del | -/AT | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74687534 | CCCAGAAGACAAAAA[-/AT]ATATATATAAATAAA | 18472 |
rs216132540 | snp | A/G | | | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74726210 | TCTTTAAAAGGTTAT[A/G]TCCAGAGTTTCAGTT | 18472 |
rs216137685 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74679032 | TGACTGCGCTTCTGA[A/G]GGTCCTCCTGAGTTC | 18472 |
rs216190734 | snp | A/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74702000 | AACTGATTATTAAAA[A/T]ATTACAAAATTCACT | 18472 |
rs216314217 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74700805 | GGTATATAAGTATAC[A/C]GTGTCTGCATGTGTG | 18472 |
rs216314348 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74715224 | CACAAACAAACAAAC[A/C]AACCAAAAAAAAAAA | 18472 |
rs216453040 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74676080 | TTCAATACTTAAAGG[A/G]ATTTTTAAAAAATCT | 18472 |
rs216554410 | in-del | -/A | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74708032 | GAGAGAGGGGGGGGG[-/A]AGGTTTTGTTTTTGG | 18472 |
rs216563902 | in-del | -/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74700856 | ATTGTGGAAGGGTGA[-/T]TGACTACAAGTGAGG | 18472 |
rs216583028 | in-del | -/TG | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74688223 | GCCAGAATTTTTTTT[-/TG]TTTTTTGTTTTTTGT | 18472 |
rs216603493 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74693869 | AATCACATTGTTTTG[A/G]GACAGAGATGGGCAG | 18472 |
rs216603658 | in-del | -/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74715066 | CCCTGTCAACTGTCT[-/C]CCCCCCCTACCCATA | 18472 |
rs216604355 | in-del | -/TACT | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74697479 | GGTCCTTAGCAAGAA[-/TACT]TAAACACTTCACACT | 18472 |
rs216616448 | in-del | -/A | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74706716 | GTAAAAATCCTACAG[-/A]AAAAAAAAAAAATCG | 18472 |
rs216925343 | snp | A/G | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74690815 | CTGAGGTGTGTGGTG[A/G]TGCATGCCTTTAATC | 18472 |
rs216987828 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74702406 | ACACAGACTTAGGTT[A/G]CATGGGAGAATATGG | 18472 |
rs217044848 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74703646 | ATGAGTTCAAGGCCA[A/G]CCTGAACTACAAAGC | 18472 |
rs217243437 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74698841 | GTATGTATGTATGAA[G/T]TAATTCCTTGCTAAA | 18472 |
rs217282681 | in-del | -/AGAG | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74697706 | ACTGATAAACGATAA[-/AGAG]ACACTATGGCAAAGT | 18472 |
rs217343368 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74685456 | CTCTTATCGACCAGA[C/T]GGTTTAAGTATGAGT | 18472 |
rs217358423 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74687342 | AAATAGTCAACGTAA[A/G]ACTGATTAACTAGGC | 18472 |
rs217497756 | snp | C/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74687665 | TTTTTGGGGGGGTTA[C/T]TTTTTATTTTTTTAT | 18472 |
rs217637110 | snp | C/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74677978 | AATTACTGAGCTTAC[C/G]AACTGGATTAGGAAT | 18472 |
rs217756290 | snp | A/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74717711 | GCAAGCACCTTTACT[A/T]TCTAAATACCCATCT | 18472 |
rs217982723 | snp | C/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74719179 | TCTGTGTAACCCTGG[C/T]TGTAGACCAGGCAGG | 18472 |
rs217994702 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74722904 | CTTAAAGGGGGGGGG[A/G]GGTGAGGAGGAGGTA | 18472 |
rs218109739 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74721124 | AGAATTGTGGGCCGG[A/G]CGCACGCCTTTAGTC | 18472 |
rs218115615 | in-del | -/AAAAC | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74680481 | GAGAGACCTTGTCCA[-/AAAAC]AAAACAAAACAACAA | 18472 |
rs218141152 | in-del | -/ACAC | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74680689 | ATTACGTTAAAAAAA[-/ACAC]ACACACACACACAAT | 18472 |
rs218162717 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74715247 | AAAAAAAAAAAAAAA[A/C]GAAAACCCAACCATC | 18472 |
rs218168023 | in-del | -/TTT | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74714823 | AATTAGTCAAAATAC[-/TTT]TTTATTAATTTAACT | 18472 |
rs218237548 | in-del | -/CAA | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74701277 | AAGAAACAACAACAA[-/CAA]CAAAATTATAAAGAA | 18472 |
rs218387391 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74680890 | AAAAATAGGGCAGCA[A/G]CAACAACAAATCCTC | 18472 |
rs218388174 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74695283 | CACTTTAAGACTGGT[C/T]GAGACACAAAATATG | 18472 |
rs218407305 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74685078 | CCTGGCTCTGCTTCC[C/T]AAGTGCTGGGATTAA | 18472 |
rs218500311 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74694496 | CTTGCCTCTGCCTCC[A/G]AAGTGCTGGGATTAA | 18472 |
rs218613991 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74681677 | ACTGCTAAAATTACT[C/T]AACTCATTAGAGTTA | 18472 |
rs218650828 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74695024 | ccagtcgatggtggc[A/G]catgcctttaatccc | 18472 |
rs218698376 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74685870 | AAATGCCCTGTCTGA[A/G]ATTAAAGTACTGTCC | 18472 |
rs218731090 | in-del | -/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74689433 | CTGTAATTTTTAGAG[-/T]TTTTTTCCCCTATAC | 18472 |
rs218842245 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74711781 | GGCCCACAACCATCC[A/G]TAACAAGACCTGATT | 18472 |
rs219000013 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74700287 | TAGGCAGTAATGAGA[G/T]ATAGCTCAGTAGAAA | 18472 |
rs219059328 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74679341 | GGCAGGAACCCATAA[G/T]GTTGAAACAGGCCTT | 18472 |
rs219200209 | snp | C/T | | | downstream-variant-500B | Pafah1b1 | Mm_Celera | 11:74673549 | CAGGAGGCACCAGCA[C/T]GAGACAGAGCACCTA | 18472 |
rs219384563 | snp | G/T | | | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74724557 | TCCCGTCCGCGGCTT[G/T]TCTCGCTTCTGCCCC | 18472 |
rs219735675 | snp | C/T | | | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74725838 | GGAATGGCTGAAGAA[C/T]GAGGATCACAAGTTT | 18472 |
rs219821428 | snp | A/G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74708032 | GAGAGAGGGGGGGGG[A/G/T]AGGTTTTGTTTTTGG | 18472 |
rs219867211 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74716063 | GAACATTAGGCCTCT[C/T]CCTTACACTTACCTA | 18472 |
rs219883161 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74719666 | TAGAACTGAACATTC[A/G]ATTTGTATTGTATTT | 18472 |
rs219891383 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74713013 | TTTGTGATAAGGTCA[A/G]CTTCTGTAGAAACTG | 18472 |
rs220068962 | in-del | -/TCTTTTC | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74691065 | TTTTATTTTTGAGCA[-/TCTTTTC]TCTTTTCTTATTTTC | 18472 |
rs220172228 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74679760 | CACTCAAGTTTATGT[A/G]GTACTGGGAACTAAA | 18472 |
rs220229040 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74688067 | TTATATCTTATACCA[A/C]AACAATGTAAAGTAT | 18472 |
rs220251472 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74713980 | TCGAGGCCAGCCTGG[C/T]CTACAGAGTGAGTTC | 18472 |
rs220296878 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74678470 | TCTCTGTGTGTGTGT[A/C]TAAGTATACATACAG | 18472 |
rs220341817 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74676643 | CCAGTATATTCTATG[C/T]ACGCTTCATTACACC | 18472 |
rs220534398 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74697368 | CTCTGCCTTCCAAAT[G/T]AAAGGTGTGTGTGCT | 18472 |
rs220714373 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74694305 | AAATCAAATTTTAAA[C/T]AGTAAAACATTATAA | 18472 |
rs221152556 | in-del | -/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74696795 | TTGTTTTTTTGTTTC[-/T]TTTTTTGTTTTTTTT | 18472 |
rs221213311 | in-del | -/TT | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74684354 | ATAAAACAATTTTTG[-/TT]TTGTTTTTATAATCT | 18472 |
rs221231231 | in-del | -/TGG | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74688215 | GTGCCCAGCCAGAAT[-/TGG]TTTTTTTTGTTTTTT | 18472 |
rs221262569 | in-del | -/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74716669 | TAAAATAAATAAATA[-/T]TTTTTAAAAGGCAAT | 18472 |
rs221380419 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74718923 | TATAAGTAAATTTGC[C/T]TTTCTCTTCAGTTTT | 18472 |
rs221499461 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74712585 | GGACAGTTCCTACTC[C/T]AGCCTCTGTGGACTC | 18472 |
rs221512924 | in-del | -/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74703292 | GAAGAACTGTATTTT[-/C]CCCCCTGGTTTTTCA | 18472 |
rs221523369 | in-del | -/AAAAC | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74705231 | AGAAACCCTGTCTTG[-/AAAAC]AAAACAAAACAAAAC | 18472 |
rs221548954 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74709417 | CAAGCAGGATGGCAC[A/T]CATGTTTAATCAATC | 18472 |
rs221554728 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74674015 | TATGCAGAAAACATG[A/G]ATAAATTTTGTTTTA | 18472 |
rs221640646 | snp | A/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74701561 | TATATATTTTATACT[A/T]GTGTAGTGAAGAATA | 18472 |
rs221643204 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74715559 | GACCATATATATGCC[C/T]TGGTGCACCTGCAGA | 18472 |
rs221713140 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74702897 | AAGATTTTTCCATAT[C/T]TTCACACCAGAACAG | 18472 |
rs221776098 | snp | C/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74678222 | TGAATTCACTGTTAT[C/G]AACTCCAGATGATAC | 18472 |
rs221798728 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74714489 | AACTTGTTTAATGAC[G/T]TCTAAATTACCTACT | 18472 |
rs221802134 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74687679 | ATTTTTTATTTTTTT[A/T]TTttttggtttttcg | 18472 |
rs221848273 | in-del | -/CACA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74698803 | TCAACTCCCATCAAC[-/CACA]CACACACACACGTAT | 18472 |
rs221969033 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74699832 | CCCAGCCATATTTTA[C/T]GTAGTTAAAACTACT | 18472 |
rs222020489 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74700970 | TGATAACCTTGTTGA[A/G]AATGGTTTTGGTCAA | 18472 |
rs222021336 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74705594 | GAATACTAACATTGT[C/T]AGCAAATCTTATGGG | 18472 |
rs222041714 | in-del | -/TGTGTG | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74704559 | AATCCACTAGTTCTT[-/TGTGTG]TGTGTGTGTGTGTGT | 18472 |
rs222174033 | in-del | -/A | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74716139 | CTCCTAGTCTTTTTT[-/A]ATCACATTTCACACA | 18472 |
rs222252974 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74687819 | TGGGATTAAAGGCGT[A/G]CGCCACCACGCCTGG | 18472 |
rs222275189 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74683197 | GGGAATTGGTTCCCA[A/C]CTCCTACCATGTAGG | 18472 |
rs222292717 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74690947 | ACCCTGTCTTGAACC[A/C]CCCCCCCAAAAAAGA | 18472 |
rs222352700 | in-del | -/AT | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74700285 | ATAGGCAGTAATGAG[-/AT]AGATAGCTCAGTAGA | 18472 |
rs222389193 | snp | A/G | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74696818 | TTTTTTTTAAAGATT[A/G]ATTGATTGATTATAT | 18472 |
rs222553012 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74691552 | AACATACTCAAACAT[C/T]GGAGATTAGAACTGA | 18472 |
rs222607327 | in-del | -/GG | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74702437 | ATTTAAGGCCAGCCT[-/GG]GTTTTTTCCCTCCAC | 18472 |
rs222633575 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74703125 | GAGTTTGAGGCCAGC[A/G]TAGGCTAGTGAGTTC | 18472 |
rs222647279 | in-del | -/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74707682 | AAGGAATAGAAAGGA[-/G]GGGCACCGAGTTGAA | 18472 |
rs222661743 | in-del | -/A | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74691966 | GTGGTGCATGCCTTT[-/A]AATCCTAGCACTAAA | 18472 |
rs222667813 | in-del | -/A | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74705275 | AAGGAGGAGGGGGGG[-/A]AGAAGGAGGAGGAAG | 18472 |
rs222696649 | in-del | -/TA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74684751 | ACATTCCAAATTAGC[-/TA]TGTTTTCTGGAAAAA | 18472 |
rs222700038 | in-del | -/A | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74690954 | TTGAACCACCCCCCC[-/A]AAAAAAGAGTAGTAA | 18472 |
rs222815262 | in-del | -/AAAAGAAAA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74705564 | CAAAAGCAAAATTAC[-/AAAAGAAAA]AAAAGAAAAAAATTG | 18472 |
rs222829198 | in-del | -/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74718816 | CTAGGCTATGTGAGA[-/C]CCCCCATATCAGAAA | 18472 |
rs222853720 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74694737 | TGCTTCTACCTCAGA[A/G]TGCTGGGATTAAAGG | 18472 |
rs222857485 | in-del | -/A | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74710748 | TAGTTATACAAAGCC[-/A]AAAAAAATATATTTA | 18472 |
rs222898871 | in-del | -/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74716200 | AAATAATTTTTATTG[-/T]TTTTTTTGGGACAGG | 18472 |
rs223042991 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74704253 | TGCTTTAAACACTCT[G/T]GAATATGAAGACATG | 18472 |
rs223050596 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74680127 | GTGCCTGTACGACAC[A/G]CTGAATGCAGTGCTC | 18472 |
rs223093402 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74705278 | GGAGGAGGGGGGGAG[A/G]AGGAGGAGGAAGAGG | 18472 |
rs223169042 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74692867 | GCCATATGTGCCACT[G/T]ATCTCCAATATTTTA | 18472 |
rs223236049 | snp | A/G | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74689261 | TTTTAGGTAGGCTGT[A/G]ACTATGAAGCTTACG | 18472 |
rs223288544 | snp | A/G | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74690689 | TTAAAATCTTTAGGG[A/G]GGGGGTAGTGGTGGT | 18472 |
rs223341570 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74691740 | AGCATAAGGGAGGTG[A/G]AAAGTGCCTGTCTGA | 18472 |
rs223402931 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74685559 | TTAGATACTGCAGCA[C/T]CGAACTCTGGCTTCT | 18472 |
rs223486520 | in-del | -/C | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74717260 | GACAAGTTTTGAGTA[-/C]CCGAGTTTAATCTCT | 18472 |
rs223621263 | snp | C/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74701237 | GTTAAGATGACTAAA[C/T]ATTGATGTGAAAAAA | 18472 |
rs223628439 | in-del | -/TTAGTCAATGCTAAAG | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74699666 | AGTTTAAAAAACAAA[-/TTAGTCAATGCTAAAG]TAAGTCCCTATCTCA | 18472 |
rs223670662 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74695581 | ACAGGCACCAATACC[C/T]ATACACATAAAATAT | 18472 |
rs223672005 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74709107 | TCAAAGAAAACAAAT[A/G]AATACTTCTAAATAA | 18472 |
rs223694795 | in-del | -/AA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74697704 | TTACTGATAAACGAT[-/AA]AGAGACACTATGGCA | 18472 |
rs223721304 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74697144 | TTTTTTTTTTCCCCC[C/T]CCCGGGACAGGGTTT | 18472 |
rs223769469 | in-del | -/TC | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74722413 | ACTCTAAATTCATAT[-/TC]TGTGTTAATAAAAAA | 18472 |
rs223800230 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74708060 | TGGTTTTGTTTTTTT[G/T]TTTTTGGTTTTTCGA | 18472 |
rs223830452 | in-del | -/TTTG | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74697112 | ATATACCAAGAATTT[-/TTTG]TTTGTTTTCCTTTTT | 18472 |
rs223898814 | snp | C/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74718027 | TTAGTCCTGTTTTAA[C/G]CAACAGTCACCAATT | 18472 |
rs223980931 | snp | A/G | | | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74725553 | AATGCTAACACTGAG[A/G]AGACGGAGGCAGGAG | 18472 |
rs224005214 | in-del | -/TTTTTTTT | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74710521 | CCATCTCTCCAGCCC[-/TTTTTTTT]TTTTTTTTTTTAAAC | 18472 |
rs224075152 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74693394 | AGGCACTTTTACCCA[A/C]TGAATCACTGAGCCA | 18472 |
rs224077129 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74678721 | AACATCTCAGTCAAG[C/T]TTCACTAGCTGGTAT | 18472 |
rs224101860 | in-del | -/A | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74718363 | GCACGGGTAGCAATT[-/A]AAAAACTAACTCTTG | 18472 |
rs224160988 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74679927 | TCCACCTTGGATGCC[A/G]GAATCATAGATATAT | 18472 |
rs224170450 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74679791 | CCCAGGGTTTTTATG[C/T]CTGTAAATACCTTTT | 18472 |
rs224173607 | in-del | -/TT | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74717465 | GCTGCTCTGTAGTTG[-/TT]TTTTGATCATAGACC | 18472 |
rs224224684 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74680650 | TTCTGGCCTACTCAG[A/G]GGCTGGCACAAACAT | 18472 |
rs224245812 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74694954 | ATATAAGGGTGTGTG[C/T]CACCAGGTTTGACCT | 18472 |
rs224296839 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74678109 | ACTGAATGTTGTGCT[C/T]CAGGCTTAGTACTAA | 18472 |
rs224340424 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74707532 | TGTAAAACACAACAT[C/T]GTGAACTAGAAAACC | 18472 |
rs224407927 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74677149 | TGTGTAATCCCCATT[A/C]CACAGATGGAGCAAA | 18472 |
rs224561135 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74682555 | TGAGGTTAGGTATAT[A/G]TAGCTAAGTGATGTA | 18472 |
rs224598348 | in-del | -/GGGA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74708029 | AGAGAGAGAGGGGGG[-/GGGA]AGGTTTTGTTTTTGG | 18472 |
rs224733404 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74692203 | GGCTAAAGAGAAACT[G/T]CTTTGAGACCCTGCC | 18472 |
rs225097858 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74679831 | gaggcacatcccAGA[A/C]ACCTGCCCCATGCaa | 18472 |
rs225157764 | in-del | -/CCTTTCCTTTTTCCCCT | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74684980 | TGTTTTGCTTCTTTC[-/CCTTTCCTTTTTCCCCT]CCTTTCCTTTCCGTA | 18472 |
rs225326551 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74698077 | GATTTGGTGGCAGTG[C/T]TGAGATGCCTAGCCA | 18472 |
rs225376996 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74686717 | TACATTTCCAATGCT[A/G]TACCAAAAGTCCCCC | 18472 |
rs225465586 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74715749 | AGGAGTACAGCTCTG[A/T]GTTAAAAGCACATAT | 18472 |
rs225614500 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74679962 | CCATGTCTGATCTTG[A/T]GCCATGCTGAGGTTT | 18472 |
rs225682611 | in-del | -/CA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74718880 | TTTAAAACTAGGACT[-/CA]CACTCTACAGCTAAG | 18472 |
rs225726623 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74696588 | ATATACCTGTCAGTG[C/T]TTTGTTGTTTTATTT | 18472 |
rs225810985 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74717572 | ACTATAGAAAAGAAG[C/T]ATTTGACCACGTAAG | 18472 |
rs225879527 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74718557 | AAATCTTAAAAAAAA[A/C]ACACAAACTACCTCT | 18472 |
rs225880297 | in-del | -/AC | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74680690 | ATTACGTTAAAAAAA[-/AC]ACACACACACAATAA | 18472 |
rs225940224 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74712802 | AAAAGACCCTGTTTC[A/C]AAACAAACAAAAAAA | 18472 |
rs226152450 | snp | C/G/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74716833 | TTAAGATAAAAAAGG[C/G/T]TAAAGAAAAGAAAGC | 18472 |
rs226232115 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74707605 | GTTCTGTAAAACAAA[A/T]TTAACGAAGTGAACC | 18472 |
rs226237842 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74687191 | AAATAGATAATATTT[A/T]AAAAAAATGCCTAGG | 18472 |
rs226299860 | in-del | -/AC | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74680694 | GTTAAAAAAAACACA[-/AC]CACACACAATAAAAA | 18472 |
rs226329127 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74713647 | ACAAACTGGGAAGAC[A/T]TGGCTCAGTAGTTAA | 18472 |
rs226389472 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74714863 | TTCAATCTTATTTGG[A/G]GGCAGATATAATGGT | 18472 |
rs226403617 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74705309 | AAGAGGAGAGAGAGA[A/G]AGAAGGATGGATGGA | 18472 |
rs226429847 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74698380 | TGTTTGTTTGTTTTT[C/T]GAGACAGGCTTTCTC | 18472 |
rs226493531 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74684857 | AACTGGCCTAAAACA[C/T]TTGATAGACCTGCCT | 18472 |
rs226518431 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74677804 | ACAGAATGCTTTGCT[C/T]GCTTTTTGAGCAGTA | 18472 |
rs226620197 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74704458 | GTAAAATAGTATGAG[C/T]CAACATGTGGCTTCT | 18472 |
rs226700197 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74687533 | TCCCAGAAGACaaaa[A/T]atatatatataaata | 18472 |
rs226852038 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74683396 | TCACACAAGTTACCT[A/G]AGGCTCTGCCCTATG | 18472 |
rs226855048 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74720552 | AAACAGACCTGTAAC[A/G]TGGATGTTCTAAACT | 18472 |
rs227027637 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74711289 | GCTGAGACGAGAACG[A/C]CCTGCTGGAGCCAGG | 18472 |
rs227054811 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74716402 | TAAGAGCACTGACTG[C/T]TCTTCCAAAGATCCT | 18472 |
rs227101467 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Pafah1b1 | GRCm38.p3 | 11:74690541 | CATATCTAGTTCAGC[C/T]TCCTTTTTAAAAACG | 18472 |
rs227108550 | in-del | -/AAAAAA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74721055 | AAAAATGAACAAGTG[-/AAAAAA]AAAAAAAAAAAAAAA | 18472 |
rs227110610 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74703571 | TAGGAAAAGTAAAAA[A/G]CCTTAGCTAGGTACC | 18472 |
rs227115783 | in-del | -/CC | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74715227 | AAACAAACAAACAAA[-/CC]AAAAAAAAAAAAAAA | 18472 |
rs227145230 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74722736 | CCCACCCCCAGAAAA[A/G]AAATTTCACACAAAA | 18472 |
rs227159693 | in-del | -/AA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74721979 | CCCTTCTTGAAGAAG[-/AA]AAAAAAAAAAGGTAG | 18472 |
rs227178264 | snp | A/C | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74715227 | AAACAAACAAACAAA[A/C]CAAAAAAAAAAAAAA | 18472 |
rs227242847 | in-del | -/TTT | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74710527 | CTCCAGCCCTTTTTT[-/TTT]TTTTTAAACTCAGGG | 18472 |
rs227289667 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74720986 | GAGTCCAATCCACAG[A/G]ACCTACATGGTGACA | 18472 |
rs227363491 | in-del | -/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74688238 | GTTTTTTGTTTTTTG[-/T]TTTTTTTTTAAAGCA | 18472 |
rs227468505 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74698495 | TGCTGGGATTAAAGG[C/T]GTGCGCCATCACGCC | 18472 |
rs227520195 | in-del | -/AA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74711917 | ATATGCACTTAATAT[-/AA]AAAAAACCAGGACAA | 18472 |
rs227602947 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74711467 | AGTTCAGGGATTTAT[A/G]ATCTGAAATTGATGC | 18472 |
rs227675819 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74708148 | GGCCTCGAACTCAGA[A/C]ATCTGCCTGCCTCTG | 18472 |
rs227774390 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74696023 | ACATGATTGTACCCA[A/G]AACTACTCTCAACCA | 18472 |
rs227777839 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74710094 | TAAAATAAACTGCCA[A/T]GTGGGTGCTGGGAAT | 18472 |
rs227804986 | in-del | -/TTC | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74692551 | AGCCAATTTTATTTT[-/TTC]TTTTCTTTTGAAAAA | 18472 |
rs227847711 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74713293 | GGGCTGGTAGGTTCT[A/C]TAAGAAAGCAAGCTT | 18472 |
rs227865906 | in-del | -/A | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74705419 | AGCATTCCAGAGGTC[-/A]AAGGCAGACTTGTTT | 18472 |
rs227965129 | in-del | -/AATA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74698009 | AGTGTACTTAAATAT[-/AATA]AATAAATAAATCTAA | 18472 |
rs228076320 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74700204 | GATGGAACATCTTTA[C/T]AGTTCAAAAAGAATC | 18472 |
rs228128053 | snp | C/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74697547 | TTTTTTAATAAAAGA[C/G]TTTCTTGGTTTGGAT | 18472 |
rs228306327 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74717053 | AGCTTTGTTTTCTTC[A/C]AGGCTTATTTTTTAA | 18472 |
rs228341782 | in-del | -/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74705808 | ACAAATGTGATAGTG[-/T]GTTTTTTTTTAAGAT | 18472 |
rs228345850 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74700337 | CTAACAACCTAAATC[C/T]CTGGGAGCCACATGG | 18472 |
rs228379717 | snp | A/C | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74701775 | TTCAAGAGGTTAAGA[A/C]AAGAATATCTTCACT | 18472 |
rs228452819 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74707643 | AAGAGGTGGAGTAAG[C/T]AACCAGTTGAGAGGG | 18472 |
rs228505964 | in-del | -/AAAAACAAC | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74701027 | AGTATTAATATTAAA[-/AAAAACAAC]AAAAACAAAATAGAA | 18472 |
rs228557309 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74719241 | TGCCTCCCAACTCTT[A/G]GATCAAAAGCTTATG | 18472 |
rs228628634 | in-del | -/AATAAATAAATAAATA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74682892 | CCCTGTCTCAAAAAT[-/AATAAATAAATAAATA]AATAAATAAATAAAT | 18472 |
rs228670218 | in-del | -/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74688888 | GAAAAAAAGATCATG[-/T]CTCTCAAAACAAAAC | 18472 |
rs228820500 | in-del | -/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74699901 | TGCTGTTTTTGAGCT[-/G]GGGGGTCTAACAAGG | 18472 |
rs228908362 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74716490 | GCCCTCTTCTGATGC[A/G]TCTGAAGATAGCCAC | 18472 |
rs229122240 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74720098 | TCACAACCACCTGTC[A/T]TCAGAGGATCCAATA | 18472 |
rs229145883 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74697462 | TTGGATTTTAGGGAC[A/T]CAGGTCCTTAGCAAG | 18472 |
rs229146323 | in-del | -/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74700636 | GTGTATAAGAGACAG[-/T]TATATGAAAGTACAT | 18472 |
rs229165695 | in-del | -/AAGCC | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74710154 | TGCTCTTACCCATTA[-/AAGCC]TTATTATTATTATTA | 18472 |
rs229215253 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74708204 | GTGCGCCACCACGCC[C/T]GGCAAGAGAGAGACA | 18472 |
rs229299443 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74703734 | GTTTGAATACTTGCA[C/T]CCACATGGCGGCTCA | 18472 |
rs229318860 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74694016 | CCTGGAAAATGATTA[A/G]GAAAGACACCTAACA | 18472 |
rs229353073 | in-del | -/AA | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74718946 | CAGTTTTTCATTGTT[-/AA]TAAAAAAAAAAAAAA | 18472 |
rs229529324 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74704502 | GAGTCCTAAGCAGGA[A/G]CAAATAATGCTCTTA | 18472 |
rs229567243 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74681016 | AGATCCATTTTTTCA[A/G]CATGGTACAAACGAA | 18472 |
rs229675275 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74717364 | TGTGCTCCCACACCC[A/G]CAACTAAAATAAAAT | 18472 |
rs229752011 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74721863 | ATTAAAAAAAAAAAA[C/T]TAGCCAGAGCATATG | 18472 |
rs229808154 | in-del | -/A | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74705570 | GCAAAATTACAAAAG[-/A]AAAAAATTGAATACT | 18472 |
rs229814759 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74684636 | CATTAAAAGTAGTAA[A/G]GGAAAAAGAGATAAG | 18472 |
rs229910179 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74680185 | CCTGGAACTGGAGTT[A/G]TAAGCTGTAACATGG | 18472 |
rs229960337 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74722894 | CCAATTGTCTCTTAA[A/G]GGGGGGGGGGGGTGA | 18472 |
rs229968277 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74683127 | TTTTGTTTATCTTTG[C/T]ATGTGTACTCCATTC | 18472 |
rs230032566 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74694112 | GTGAGGTAAAGAGAG[A/G]ACCCAGATTAGATTC | 18472 |
rs230085478 | in-del | -/A | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74723182 | TCAGCCCACCGTCTC[-/A]AAAAAACATTTTCTC | 18472 |
rs230169900 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74720735 | GCACTCAGGCGGCCT[C/T]TAAGGTAGAAAAAAG | 18472 |
rs230424584 | in-del | -/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74722895 | CAATTGTCTCTTAAA[-/G]GGGGGGGGGGGTGAG | 18472 |
rs230473702 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74692264 | TAGAATGACATTTAG[A/T]ATTATACTTTAAAGG | 18472 |
rs230488651 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74693724 | AGTGAGATCCAGATT[C/T]AGTTAAAAGATCCTG | 18472 |
rs230512203 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74692737 | CTTAAGTAGGACGGT[C/T]GTACCTTGAACTTCT | 18472 |
rs230575237 | snp | A/G | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74688779 | CAAGTCTGCCTTTCA[A/G]AGAAATTTACCTTAC | 18472 |
rs230596328 | in-del | -/AAT | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74718310 | AAAAGAAGCAACCAA[-/AAT]AATAAGTATTTATGA | 18472 |
rs230663206 | snp | G/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74705810 | CAAATGTGATAGTGG[G/T]TTTTTTTTAAGATTA | 18472 |
rs230690494 | snp | C/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74701830 | TTATGAGTTTCAAGG[C/T]CAGTCTGGGTTGTCT | 18472 |
rs230732717 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74703193 | TCAAGAAAGGATACT[A/G]GAATACGCACTCTCA | 18472 |
rs230906757 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74693295 | ATTATCCTTGTCTGT[A/G]TATGTGGGGTAAGGT | 18472 |
rs230932528 | in-del | -/CA | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74695536 | ACGCACACGCGCACG[-/CA]CACACACACACAGAG | 18472 |
rs231045348 | snp | C/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74689214 | GAAGTTAAACAAAGT[C/T]GTGTTTTATAATATA | 18472 |
rs231111359 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74717828 | TTGAGAGCCAGGCAG[C/T]GGTGGCGCATGCCTT | 18472 |
rs231133509 | in-del | -/AAAAA | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74719617 | ACAAAACAAACAACC[-/AAAAA]AAAAAAAAAAAAAAA | 18472 |
rs231165491 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74705297 | AGGAGGAAGAGGAAG[A/G]GGAGAGAGAGAAAGA | 18472 |
rs231167264 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74719438 | TTCTATTAGAAGCAA[C/T]TAAAAATTCTGTCCA | 18472 |
rs231281250 | in-del | -/AAA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74705236 | CCCTGTCTTGAAAAC[-/AAA]ACAAAACAAAACAAA | 18472 |
rs231311421 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74677946 | TTCTCCATATACATA[A/C]CCATCCATATCTCTA | 18472 |
rs231321518 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74719103 | CAAAAAACCAACCAA[A/C]CAAACAAACAAACAA | 18472 |
rs231570041 | snp | C/G | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74689283 | AAGCTTACGGTAGTC[C/G]AGAACTTAGGATCTT | 18472 |
rs231620725 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74678975 | TGAAAACTTTTTTTT[A/T]AAAGATTTCTTTTAG | 18472 |
rs231746193 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74678093 | CCCAGCATATTGATT[A/T]ACTGAATGTTGTGCT | 18472 |
rs231763703 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74678593 | CTACCAGCTGAACCA[G/T]CTTGCTAGCCCTATT | 18472 |
rs231766396 | in-del | -/AATT | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74681468 | CAATATTCCCTTCTC[-/AATT]AATCCTGTAGTATAC | 18472 |
rs231877431 | in-del | -/GAACAAACAAGT | | | cds-indel | Pafah1b1 | Mm_Celera | 11:74675939 | TCTGAGGAATATTAA[-/GAACAAACAAGT]GAACAAACAAAAGCA | 18472 |
rs231991216 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74716568 | TGGGACTGACCAGAG[A/C]GAGCAGAGGTAGGTC | 18472 |
rs232083199 | snp | A/G | | | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74725640 | AATGATTTAAAGCTG[A/G]ACATGGTGTTTTAAT | 18472 |
rs232183174 | snp | A/G | | | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74724669 | TCACTGCGCTGTCCC[A/G]GCGGACCGCGGGTAC | 18472 |
rs232220949 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74687290 | GCTTTTAATGGCTAA[A/G]CCATCTTCTCCAGCC | 18472 |
rs232249502 | snp | C/T | | | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74726085 | CTCTTTGTATTGGGA[C/T]GGGCTATCTTTATCC | 18472 |
rs232319769 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74705237 | CCTGTCTTGAAAACA[A/C]AACAAAACAAAACAA | 18472 |
rs232345658 | snp | C/T | | | downstream-variant-500B | Pafah1b1 | Mm_Celera | 11:74673876 | TTTCTGTTGCTGGTG[C/T]CCAAGTCTCACTTCC | 18472 |
rs232363108 | snp | A/G | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74701642 | AACTTGTAGTAAGTA[A/G]AGGGCAGGGGAACAA | 18472 |
rs232405023 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74697415 | TTGGATCCTCTGGAG[C/T]TGGAATTACAATGAG | 18472 |
rs232496951 | in-del | -/GG | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74693897 | AGATCCCAGGAGTGA[-/GG]GCTAGCCAGTGAGAG | 18472 |
rs232521323 | in-del | -/TAA | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74690305 | AGAAAAAGTAAGATT[-/TAA]AAAAAAAAAAAATGG | 18472 |
rs232794244 | in-del | -/AA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74685798 | CACATCAAAGCAGAC[-/AA]AACTAGGAATTAAAT | 18472 |
rs232909247 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74713516 | AGGAATACAAACCCT[A/G]AGACAATCACTTTGG | 18472 |
rs232955373 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74699743 | AACCAAACCAAAAAA[A/C]CCCAAAAACTGCTAT | 18472 |
rs232956275 | snp | C/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74688363 | TTAACTTCAATCATA[C/T]ATTCAAGCATATCTA | 18472 |
rs233056601 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74685758 | TAACAAAAACCTCTA[C/T]CACTAAAGCTTGTTC | 18472 |
rs233122111 | in-del | -/TTTAAACTTGG | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74698920 | TGCTGGTAAAAATAC[-/TTTAAACTTGG]TTTAAACTTGGGACT | 18472 |
rs233136580 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74682706 | ATATATAACAACCAT[C/T]AGAGGGTACTACAAA | 18472 |
rs233139032 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74675532 | TTTGCTCCTCTACAT[A/T]GGTACCATTCTTTAT | 18472 |
rs233188964 | in-del | -/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74689235 | TATAATATATTTGGG[-/T]TTTTTTTCCCTTTTA | 18472 |
rs233240324 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74686602 | TACCTATGGAGTGCT[A/G]GGATTAAAGGTGTGT | 18472 |
rs233305861 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74696277 | AAAACAAAAACAAAA[A/C]CAAAACACAGGCACA | 18472 |
rs233490283 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74724271 | CGCTCCCTGGACTCT[A/C]GGCTCGCTGCTCCTT | 18472 |
rs233613608 | in-del | -/TGTA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74707513 | ATATTTGATCACACT[-/TGTA]GTAAAACACAACATT | 18472 |
rs233637585 | in-del | -/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74704139 | TTATTTTAAGGTCAC[-/T]ATTTTTTTTTAATTT | 18472 |
rs233638141 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74714607 | AGTATACATGTAAGG[A/C]GTTTCCATGCTCTTG | 18472 |
rs233708982 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74709832 | GAGGGTGTTGGATCC[A/C]CTGGAACAGGAGTTA | 18472 |
rs233710773 | in-del | -/ACAA | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74715210 | TCAATTCCCAGTATC[-/ACAA]ACAAACAAACAAACC | 18472 |
rs233848203 | snp | C/T | | | intron-variant, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74723606 | CCCTTTCCCCAAGAT[C/T]AGAGAGCGACCTGCT | 18472 |
rs233901452 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74715617 | TATATGGGTTCTGGG[A/G]ATCCAACTCAGGTCA | 18472 |
rs234087642 | in-del | -/TGTA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74681882 | CAACTCACACCAGTC[-/TGTA]TGTAACTCTATCTAG | 18472 |
rs234198058 | in-del | -/AC | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74719633 | AAAAAAAAAAAAAAA[-/AC]ACCCTATATCACAGC | 18472 |
rs234295140 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74708627 | AAAAAACACACAATT[A/T]TAAAAAAATGTTAGT | 18472 |
rs234310294 | in-del | -/TT | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74688541 | TGAATTCATTCTTTC[-/TT]ATTTATTTAGTTATT | 18472 |
rs234355226 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74696736 | AGGACCTCTGGAAGA[C/T]GTGCTTGCTCTCAAC | 18472 |
rs234370417 | in-del | -/AAC | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74701266 | AATAGACACAAAAGA[-/AAC]AACAACAACAACAAA | 18472 |
rs234509636 | snp | G/T | | | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74725925 | GAGACAGCTCAGTAG[G/T]AGAGTACTTGCTGAG | 18472 |
rs234554775 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74710656 | CATGTGGTTGCTGGG[A/T]GTTGAACTCAGGACC | 18472 |
rs234639368 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74721488 | TAGCCTTTCTACTTC[A/C]TAATGGACATGGAAA | 18472 |
rs234822052 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74706899 | TAGATTATTGTTGGT[A/G]AATGTGTTAGCCCAG | 18472 |
rs234888387 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74707836 | CTCTATCACTTTCTA[C/T]CTTATATTTTTTTTA | 18472 |
rs234937926 | in-del | -/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74687535 | CCAGAAGACAAAAAA[-/T]ATATATATAAATAAA | 18472 |
rs235022377 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74696506 | AAAGAAAGAAGGAAC[C/T]ATGTACATACAGGAT | 18472 |
rs235048789 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74722332 | GCAGCTTTAAATATA[C/T]TACAGAAAATCCTTC | 18472 |
rs235166161 | in-del | -/C | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74680047 | TACTCTTAAGATAGA[-/C]TAGTATTCTTCCAAA | 18472 |
rs235169568 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74695159 | AAAAACCAAAAAAAA[A/T]AAGTTTCCTTACAGA | 18472 |
rs235187748 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74720799 | AGAGAATTAAGCCAG[G/T]CAAGAGTGTCTGTAA | 18472 |
rs235209308 | snp | A/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74716834 | TAAGATAAAAAAGGT[A/T]AAAGAAAAGAAAGCA | 18472 |
rs235229454 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74686372 | TGTATGTAGAACAGT[A/G]GACTGACTTAAGGTC | 18472 |
rs235344847 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74698886 | TGAAGGCAAGACAGT[A/G]TCAACAATAATATAG | 18472 |
rs235346263 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74684961 | AAATACCAGATAATC[G/T]TTTTGTTTTGCTTCT | 18472 |
rs235379221 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74706327 | GTAAATTTGGGTTTT[G/T]TTTTTAAAGATTTAT | 18472 |
rs235564904 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74680897 | GGGCAGCAACAACAA[A/C]AAATCCTCATATATT | 18472 |
rs235623754 | in-del | -/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74698179 | GGCATAACTATGCAA[-/C]CCCCCCCACACACAC | 18472 |
rs235625994 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74681793 | TCTTTAAAAAGTACT[G/T]GTGAGATGGCTCAGT | 18472 |
rs235706966 | snp | C/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74692140 | aaacatgcagatctc[C/G]gagtttgaggccagc | 18472 |
rs235825274 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74695482 | GCAGTCTGGCCTCCA[C/T]AGGGACCAGGTACAC | 18472 |
rs235992962 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74708000 | CTCTCTCTCCCCCTC[C/T]CTGTCTCCCCCACAG | 18472 |
rs236022272 | in-del | -/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74711855 | CAATATATTAAAAAA[-/C]ACACACACACTCTCT | 18472 |
rs236089802 | in-del | -/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74685011 | CCTTTCCTTTCCGTA[-/T]TTTTTTGGCTGTCCT | 18472 |
rs236123243 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74695109 | ACAGAGTGAGTTCCA[A/G]GGCAGCCAGGGCTAC | 18472 |
rs236140163 | in-del | -/CATGCACGCACACGCGCACG | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74695517 | CTATGCGCGCGCGCA[-/CATGCACGCACACGCGCACG]CACACACACACAGAG | 18472 |
rs236219930 | in-del | -/TGATTAGATGGG | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74694578 | CAGAAGTATACAGGC[-/TGATTAGATGGG]ATAACTAAACACAGG | 18472 |
rs236272700 | in-del | -/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74692964 | TAGATTCTGTTTTTG[-/T]TTTTTTTCCTTTCTT | 18472 |
rs236349214 | in-del | -/ATCTC | | | downstream-variant-500B | Pafah1b1 | Mm_Celera | 11:74673687 | TGGAATTGAGTCTGT[-/ATCTC]TAAGAGACAGTAAGT | 18472 |
rs236373094 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74702451 | TGGGTTTTTTCCCTC[C/T]ACCAAGAATCACTTC | 18472 |
rs236421635 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74692568 | CTTTTCTTTTGAAAA[A/C]CAGTCTTTGTGTCTT | 18472 |
rs236467727 | in-del | -/CTGCCTCTGCCT | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74707428 | AATTCAGAGATCAGC[-/CTGCCTCTGCCT]CTGCCTCTGCCGGCA | 18472 |
rs236569370 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74705066 | AAGCACATATATTTT[A/C]ATTTTATTCAACAGA | 18472 |
rs236581823 | in-del | -/TAAAATGGA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74722779 | CAAAAAGAGAATTGC[-/TAAAATGGA]TAAAATGACCTTTAT | 18472 |
rs236737946 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74687099 | AGTTTAGACCACTCT[A/T]CCTACAGTGGGCACA | 18472 |
rs236757369 | in-del | -/A | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74718549 | TAATAAATAAATCTT[-/A]AAAAAAAAACACAAA | 18472 |
rs236802979 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74687828 | AGGCGTGCGCCACCA[C/T]GCCTGGCCCAGATTT | 18472 |
rs236880700 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74699843 | TTTACGTAGTTAAAA[C/T]TACTACTTTCAATGA | 18472 |
rs236906068 | in-del | -/A | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74701369 | CCAGCCTGGCCTCAC[-/A]AGAGATATGCCTGCC | 18472 |
rs237005629 | in-del | -/TT | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74706537 | GAGACAGGGTTTCTG[-/TT]TAATCCTAGAACTCA | 18472 |
rs237034351 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74708170 | CTGCCTCTGCCTCCC[A/G]AGTGCTTCGATTAAA | 18472 |
rs237072730 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74705107 | TCCATATGACTTTGA[A/T]GCACACCCCCAATAA | 18472 |
rs237236037 | snp | C/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74716156 | TCACATTTCACACAA[C/G]TCTGAATTCAATCAA | 18472 |
rs237259672 | snp | C/G | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74717713 | AAGCACCTTTACTTT[C/G]TAAATACCCATCTAC | 18472 |
rs237295946 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74716947 | CAGGAGTGTCCCACG[A/C]CTTCCATAGAGAGAC | 18472 |
rs237323499 | snp | A/G/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74715248 | AAAAAAAAAAAAAAA[A/G/T]AAAACCCAACCATCT | 18472 |
rs237361489 | snp | C/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74702429 | GAATATGGATTTAAG[C/G]CCAGCCTGGGTTTTT | 18472 |
rs237419107 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74712339 | AATAGGTACAAAAGG[A/G]ATATATATAATTGCA | 18472 |
rs237605539 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74715258 | AAAAAGAAAACCCAA[C/T]CATCTGTCATAAATC | 18472 |
rs237665119 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74676617 | TAAACAAAACATGAG[-/A]AAAAAAAAACCCAGT | 18472 |
rs237790386 | snp | A/G | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74717658 | ATTTGTAGAATTTTG[A/G]ATCTCAAAGTTCAAA | 18472 |
rs237817540 | in-del | -/TTCT | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74714363 | TTCAAACAGTAATCA[-/TTCT]TTTCATTCTTTTCTG | 18472 |
rs237861676 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74694218 | CATGTACACAATGCA[C/T]AGTCATACACATAAG | 18472 |
rs237906154 | in-del | -/T | | | upstream-variant-2KB | Pafah1b1 | GRCm38.p3 | 11:74726151 | TTAAGGGATTAGTTC[-/T]TTTTTTTTTTTTCTT | 18472 |
rs237912062 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74677720 | ACTGCCAGTAACCAC[A/G]TAGGGTGCCGTCTTA | 18472 |
rs237912159 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74691621 | AATACAAAGAGAAGA[A/C]TCAGTGGTTATCATC | 18472 |
rs237915495 | in-del | -/CA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74720142 | ACACTTACAACTAGC[-/CA]CACACACACTCATGT | 18472 |
rs237944211 | snp | A/G | | | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74726252 | TAGTCAAAACTATGG[A/G]CAGCATGAGACAGAG | 18472 |
rs237944982 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74680409 | TACACACCCTTAATC[C/T]CAGCACTCAAGAAGC | 18472 |
rs237972426 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74678231 | TGTTATCAACTCCAG[A/G]TGATACTGAGGACAT | 18472 |
rs238033818 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74700288 | AGGCAGTAATGAGAG[A/C]TAGCTCAGTAGAAAA | 18472 |
rs238045664 | snp | C/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74689815 | TTGTATTGTGGTGAC[C/T]CCCAATTATAAAATT | 18472 |
rs238121512 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74687721 | CTCTGTATAGCCCTG[A/G]CTGTCCTGGAACTAA | 18472 |
rs238125282 | in-del | -/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74718738 | TTTTCTTGAAATGCC[-/T]TTTTTTTTTTGAGGT | 18472 |
rs238126501 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74704088 | TGATACATGTCTATA[A/G]TCAGAGAAAGTATTT | 18472 |
rs238164232 | in-del | -/TGTA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74720396 | CTTTTTACCATTATG[-/TGTA]TGTGTCAGTCAGAGG | 18472 |
rs238182096 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74674219 | TGTCAGTGTCAGGAC[C/T]GGCTTCTAACTCGTA | 18472 |
rs238200235 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74691120 | ACTCAGAACACTGTA[C/T]ATGCTAGGTAAGTAA | 18472 |
rs238382049 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74684696 | CTATCTTTGATGATG[A/T]TCACAGGAGAAAATG | 18472 |
rs238498467 | snp | C/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74721137 | GGGCGCACGCCTTTA[C/G]TCCCAGCACTTGGAG | 18472 |
rs238816102 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74687487 | TTACAGAGAAACCAT[A/G]TCTCAAAAAAATGAA | 18472 |
rs238835524 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74678534 | AGGAGCCATGTGGGA[C/T]GTGGAGATTAAGCAT | 18472 |
rs238836316 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74681482 | CAATTAATCCTGTAG[A/T]ATACTTTAAGGCGTT | 18472 |
rs238880460 | in-del | -/AAACAAAAC | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74683981 | AAACCCAGATAAGAA[-/AAACAAAAC]AAAAAAAAAATAACA | 18472 |
rs238899212 | in-del | -/A | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74703015 | TGTAACATATATCCC[-/A]TTTGATTATAGGGGT | 18472 |
rs239117316 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74702798 | aaatcaacacacccc[A/C]aaaaaaggtcagcat | 18472 |
rs239282555 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74698183 | ATAACTATGCAACCC[A/C]CCCACACACACATGC | 18472 |
rs239417289 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74697420 | TCCTCTGGAGTTGGA[A/C]TTACAATGAGTTGTA | 18472 |
rs239419594 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74711254 | GGTAGAGACATCTTG[A/G]GAGCCCTGGGCCAGA | 18472 |
rs239434768 | in-del | -/ATAC | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74687134 | TAAATGTCATAGGGA[-/ATAC]ACACACACACACACA | 18472 |
rs239467870 | in-del | -/ACCC | | | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74724785 | CCCCATCCCCCACCT[-/ACCC]ACCCACCCACCCAAA | 18472 |
rs239530965 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74688120 | gttttgagacaaagt[A/C]tcattatctagatca | 18472 |
rs239565379 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74714033 | AGAAACCCCGTCTCG[A/G]AAAAAAAAAAAAAAA | 18472 |
rs239615584 | in-del | -/GTTTTTTC | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74698380 | GTTTGTTTGTTTTTT[-/GTTTTTTC]GAGACAGGCTTTCTC | 18472 |
rs239652231 | in-del | -/AAAAA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74721247 | AGAAACCCTGCCTCC[-/AAAAA]AAAAAAAAAAAAATT | 18472 |
rs239704509 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74713080 | TTTCAATGTCTTAAT[A/G]AATAGAATTTTGGAG | 18472 |
rs239753271 | in-del | -/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74716833 | TTAAGATAAAAAAGG[-/T]TAAAGAAAAGAAAGC | 18472 |
rs239787246 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74716831 | AATTAAGATAAAAAA[A/G]GTTAAAGAAAAGAAA | 18472 |
rs239867072 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74709868 | CATTATAAACTGCCA[A/T]GTGGGGCTGGTGAGA | 18472 |
rs239885632 | snp | A/T | | | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74724590 | GATCCCTTGGGAAGC[A/T]TCCCTTTTGCTCTAA | 18472 |
rs239954908 | snp | C/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74720545 | TTAAATAAAACAGAC[C/G]TGTAACGTGGATGTT | 18472 |
rs239960255 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74685115 | CACCAAAACTGTCAG[A/G]ACTGTTTTGATTTCT | 18472 |
rs240125623 | in-del | -/A | | | downstream-variant-500B | Pafah1b1 | Mm_Celera | 11:74673930 | CCCCAATGACCATTG[-/A]AAAAAACCCCACCAG | 18472 |
rs240150702 | in-del | -/AT | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74706159 | ATTACCCTACGAATC[-/AT]AGTAAAACTAAGACC | 18472 |
rs240208397 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74682909 | ATAAATAAATAAATA[A/G]ATGGATAGGTAAATA | 18472 |
rs240348066 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74678119 | GTGCTTCAGGCTTAG[C/T]ACTAATGCAACACTC | 18472 |
rs240348702 | snp | A/C | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74688935 | CCAAAAAAACAAAAA[A/C]CACAAAACAAAAAGC | 18472 |
rs240497688 | in-del | -/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74719728 | TTTTGGTTTTGTTTT[-/G]GGGGGTTCAAGGGAA | 18472 |
rs240512589 | snp | A/G | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74701661 | GCAGGGGAACAAATA[A/G]CCTTAGAAAGCAAAT | 18472 |
rs240527730 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74683207 | TCCCACCTCCTACCA[C/T]GTAGGTTCAGGAATC | 18472 |
rs240717107 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74696983 | CCACTGAGCCATCCT[G/T]CCAGCCCCTATCAGT | 18472 |
rs240911254 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74694666 | AGACTTCAAGTCATA[C/T]CCCATCCCCCTTTTT | 18472 |
rs241190718 | in-del | -/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74687654 | GATTTATCTTTTTTT[-/G]GGGGGGGTTATTTTT | 18472 |
rs241258085 | in-del | -/AACC | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74719093 | ATCCAAATCTCAAAA[-/AACC]AACCAACCAAACAAA | 18472 |
rs241267501 | in-del | -/AG | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74693224 | AACTATTCCACTCAA[-/AG]ACAATTTCCATACAT | 18472 |
rs241322728 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74718558 | AATCTTAAAAAAAAA[A/C]CACAAACTACCTCTT | 18472 |
rs241351833 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74705313 | GGAGAGAGAGAAAGA[A/T]GGATGGATGGAAGTT | 18472 |
rs241352208 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74691981 | AAATCCTAGCACTAA[A/T]GAGGCTAAGACAGGA | 18472 |
rs241392836 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74681287 | TATGTGCTGCTGCTG[C/T]TACCACCACTTCCGA | 18472 |
rs241485280 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74708047 | AAGGTTTTGTTTTTG[G/T]TTTTGTTTTTTTGTT | 18472 |
rs241559979 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74719674 | AACATTCGATTTGTA[C/T]TGTATTTTGCTTTGG | 18472 |
rs241582812 | in-del | -/TA | | | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74676529 | CAACAACATGGAGGT[-/TA]TATGTGTGTGATATA | 18472 |
rs241598037 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74707042 | AGCTTAGGCATGAAC[A/G]ATAGAAAACATCCAC | 18472 |
rs241615707 | in-del | -/A | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74710742 | ACTTTTTAGTTATAC[-/A]AAGCCAAAAAAAATA | 18472 |
rs241677027 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74676468 | TGTTCCCCAGCAAGA[-/T]TTACTCTATGCGTAA | 18472 |
rs241816802 | snp | A/G/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74695508 | TACACACACCTATGC[A/G/T]CGCGCGCACATGCAC | 18472 |
rs241841072 | in-del | -/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74681047 | CCTAGAATACAATAG[-/T]TTTTTTTCTGAGAGA | 18472 |
rs241899552 | in-del | -/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74691252 | CTCTAGATATATTTC[-/T]TTTTTTTTTTTAAAG | 18472 |
rs241904679 | in-del | -/TT | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74691251 | CTCTAGATATATTTC[-/TT]TTTTTTTTTTTTAAA | 18472 |
rs241954625 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74714754 | AATCCTACCTCTCTT[C/T]GACTTTTGAGAGATC | 18472 |
rs242036460 | snp | A/T | | | downstream-variant-500B | Pafah1b1 | Mm_Celera | 11:74673589 | GAAGACTTACTCTGG[A/T]ATATTTCATAAAACC | 18472 |
rs242110128 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74679952 | ATATATACTACCATG[C/T]CTGATCTTGTGCCAT | 18472 |
rs242165656 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74704239 | CACGCTTGGCACACT[A/G]CTTTAAACACTCTGG | 18472 |
rs242187270 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74720346 | TATCCAGATAGCTTC[A/G]CATATAATCTAAGAG | 18472 |
rs242213901 | in-del | -/AGA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74708020 | CTCCCCCACAGAGAG[-/AGA]GGGGGGGGGAAGGTT | 18472 |
rs242236030 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74682378 | ATTATTTTTCCCATA[C/T]AAAAAATAAGGACTT | 18472 |
rs242239668 | snp | C/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74697145 | TTTTTTTTTCCCCCC[C/G]CCGGGACAGGGTTTC | 18472 |
rs242300509 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74683743 | CACTAGAACACTTTC[C/T]AAAAGTGACACAAAT | 18472 |
rs242309288 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74719394 | TAAAAGTAGGCTACC[A/G]GTCATTATAAAATAC | 18472 |
rs242370650 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74695781 | TTCATCTCTTTACAT[A/G]CATACACATATACAC | 18472 |
rs242510227 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74707606 | TTCTGTAAAACAAAA[A/T]TAACGAAGTGAACCA | 18472 |
rs242555049 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74692254 | AATAACGTCTTAGAA[C/T]GACATTTAGAATTAT | 18472 |
rs242616076 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74678740 | ACTAGCTGGTATACT[A/G]CAGTATCAGGGATTG | 18472 |
rs242685931 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74690972 | AAAAGAGTAGTAAAT[G/T]ATATAAATATTTCTG | 18472 |
rs242804741 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74719472 | CTAGTTCAGTGATGG[A/G]TAACACCCAAGAGGC | 18472 |
rs242856114 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74681548 | CGTAGTTTCTAAAAC[C/T]ATGATGTTATATTCT | 18472 |
rs242876243 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74703201 | GGATACTGGAATACG[C/T]ACTCTCATATTGCTT | 18472 |
rs242901292 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74712027 | gaaggaaagaaacaa[A/C]tagaagttaagtttt | 18472 |
rs242931967 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74679764 | CAAGTTTATGTAGTA[C/T]TGGGAACTAAACCCA | 18472 |
rs243037013 | in-del | -/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74708528 | ATTCCACGCATCCCA[-/C]AGAGTGGAAGGGGAA | 18472 |
rs243091061 | snp | C/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74685257 | gctTGTTTTAAAATC[C/G]CTAACACAGCATTTG | 18472 |
rs243095025 | in-del | -/AAC | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74709275 | AAAACAAATCACCAA[-/AAC]AACAACAAAACTTTT | 18472 |
rs243172483 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74679099 | GTAATGAGATCTGAC[A/G]CCCTCTTCTGGAGTG | 18472 |
rs243242992 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74685411 | CATTGTGAGAACCCG[C/T]CCCAGAAATCTAAAA | 18472 |
rs243254427 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74722313 | CTTAAAATTATATAT[A/G]CCAGCAGCTTTAAAT | 18472 |
rs243303075 | snp | C/T | | | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74726029 | GCCTGAGGTTTGATG[C/T]GTAACTCATGTAACC | 18472 |
rs243417268 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74705693 | TTTTGTTTTGACCCA[C/T]ACAATGAAAAAGAAC | 18472 |
rs243460238 | in-del | -/AAAAAAAA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74682436 | TACTTGAAATCTTGC[-/AAAAAAAA]AAAAAAAAAGCTGTT | 18472 |
rs243463245 | in-del | -/TA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74692613 | TACAGAGATATGGCC[-/TA]ACCCTGCCATATCTC | 18472 |
rs243573653 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74706918 | gtgttagcccagcat[C/T]caagaggtagaaagc | 18472 |
rs243679909 | in-del | -/A | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74707607 | CTGTAAAACAAAATT[-/A]AACGAAGTGAACCAT | 18472 |
rs243942221 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74700042 | AAATTTACCTGTCTA[A/C]TTTCTATTATTAATA | 18472 |
rs243967738 | in-del | -/TCA | | | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74676661 | CTTCATTACACCCTG[-/TCA]TCACTTTTTTTTATA | 18472 |
rs244008944 | snp | A/G | | | downstream-variant-500B | Pafah1b1 | Mm_Celera | 11:74673644 | AGGTAAGAGATGATA[A/G]ATACAAAATGGGCAG | 18472 |
rs244010551 | snp | A/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74688564 | TTAGTTATTTATTTA[A/T]TGTATAGGAGTACAA | 18472 |
rs244024640 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74687192 | AATAGATAATATTTT[A/T]AAAAAATGCCTAGGC | 18472 |
rs244050459 | in-del | -/AA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74695150 | CTGTCTCGAAAAACC[-/AA]AAAAAAAATAAGTTT | 18472 |
rs244074329 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74714956 | AGGCTTAAACTAGAC[A/C]ACATTACAAGGTAGC | 18472 |
rs244108374 | in-del | -/TGTT | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74708311 | TCCCCAGCCCCAAGA[-/TGTT]TGTTTTCTCTAGGGT | 18472 |
rs244264619 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74675850 | ACAGTGTTGTTTATG[A/G]GAGTCACGATGGAGT | 18472 |
rs244265087 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74697392 | GTGTGCTTCTGATGT[G/T]AGAGGCATTGGATCC | 18472 |
rs244340089 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74705634 | AGTACGGCTCACTGT[A/T]TGATCCTCAGCAGCA | 18472 |
rs244585204 | in-del | -/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74694248 | GACAAAATACTTATA[-/C]ACATATTAAAAAAAG | 18472 |
rs244672101 | in-del | -/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74705675 | ACACCCAGTTTCTAG[-/T]TTTTTTGTTTTGACC | 18472 |
rs244682151 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74676054 | TTGTCCTTTCAGGAA[C/T]CAAATTTCCATTCAA | 18472 |
rs244693906 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74703152 | GTTCCAGAACAGCCA[A/G]AGCTGCAGAAGGAGA | 18472 |
rs244734498 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74677817 | CTTGCTTTTTGAGCA[A/G]TATATTTTATATAAG | 18472 |
rs244743033 | in-del | -/TT | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74679686 | TACTAAAACCAGTCC[-/TT]TTTTTTCTTTTTTCT | 18472 |
rs244782165 | in-del | -/A | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74722085 | ATCATTAAGGATGAG[-/A]AAAAAACCCAGTGAA | 18472 |
rs245041828 | in-del | -/TGAT | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74683012 | TATGGAGGAGGGGTC[-/TGAT]TGATTATGAATCATC | 18472 |
rs245044827 | in-del | -/A | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74719618 | ACAAAACAAACAACC[-/A]AAAAAAAAAAAAAAA | 18472 |
rs245118523 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74675208 | AGCAGACAGAGAAAA[C/T]AGTAACATAAGAGTA | 18472 |
rs245273245 | in-del | -/AAAC | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74689649 | TCTTATATATTAAAG[-/AAAC]AAACAAACAAACAAA | 18472 |
rs245408196 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74685248 | ATTCACCTGGCTTGT[C/T]TTAAAATCGCTAACA | 18472 |
rs245428235 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74710419 | AAGAGGGCATTGGAT[C/T]CCATTATAGATGGTT | 18472 |
rs245562565 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74704337 | ACTTTTCAAGTTTTT[A/G]AAATTTTATGTGTAT | 18472 |
rs245631672 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74691859 | TCTCCAGGCAGATAC[A/T]CACACATGCACCATA | 18472 |
rs245636383 | in-del | -/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74680842 | TATGTCATAAAACCC[-/T]GTCTCAAAAACAAAA | 18472 |
rs245721224 | in-del | -/TAATA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74678824 | TAGCACTTAAGCCTT[-/TAATA]TAATACATCCTCATG | 18472 |
rs245785672 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74683375 | CCAGAGACCTTAGAC[A/T]GAAAATCACACAAGT | 18472 |
rs245788703 | in-del | -/CT | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74692612 | TTACAGAGATATGGC[-/CT]CACCCTGCCATATCT | 18472 |
rs245798016 | in-del | -/ATTAAAGGC | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74685089 | TTCCCAAGTGCTGGG[-/ATTAAAGGC]AACACCAAAACTGTC | 18472 |
rs245838091 | snp | C/G | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74685097 | TGCTGGGATTAAAGG[C/G]AACACCAAAACTGTC | 18472 |
rs245921870 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74720456 | ACCATGTGGACACTG[G/T]GGATCAAACTCATAC | 18472 |
rs245977161 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74707743 | CTTTAAACAAGTCTG[A/G]TATTTGTTCTTGGTT | 18472 |
rs246054299 | in-del | -/GTTGGAT | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74706311 | AGTACTTGGGGTTGA[-/GTTGGAT]GTAAATTTGGGTTTT | 18472 |
rs246149121 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74698839 | ATGTATGTATGTATG[A/T]AGTAATTCCTTGCTA | 18472 |
rs246157127 | in-del | -/A | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74715793 | TTTAAGCCAACACTT[-/A]AAAATATTTTTAATT | 18472 |
rs246172134 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74688133 | GTCTCATTATCTAGA[A/T]CATGTTGGCCTTAAA | 18472 |
rs246190437 | in-del | -/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74682029 | TGAACTAAGACCCTA[-/C]CCCCCCAGCACTGAC | 18472 |
rs246200842 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74700247 | TTCAGAAATATTACT[G/T]AACAATGAATGAACC | 18472 |
rs246210472 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74710682 | GGACCTCTGGAAGAG[C/T]TATCAGTGCTCTTAA | 18472 |
rs246237979 | snp | C/T | | | intron-variant, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74723494 | CGGAGAACCCGACGC[C/T]TGGAAGGCCTGGTAG | 18472 |
rs246570810 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74697525 | CAACTCTCTTACCCC[C/T]TTTTTCTTTTTTAAT | 18472 |
rs246570818 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74682993 | TATTAATATGTAGGG[G/T]GTTTTATGGAGGAGG | 18472 |
rs246695732 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74696518 | AACCATGTACATACA[A/G]GATGGAATTATAAGA | 18472 |
rs246820025 | in-del | -/AAAAA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74712829 | AAATCCAAACAAAAC[-/AAAAA]AAGGTAAATAAAAAT | 18472 |
rs246942358 | in-del | -/CTAA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74708401 | TTCCTCAACTGGTTT[-/CTAA]CTATTATCCACACTT | 18472 |
rs247096749 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74708154 | GAACTCAGAAATCTG[C/T]CTGCCTCTGCCTCCC | 18472 |
rs247268543 | snp | A/G | | | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74725421 | GCCCAAGCTACTCAG[A/G]AGGCAGGAGACCAGC | 18472 |
rs247270137 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74711338 | AGTAGCACAGGAATA[C/T]ATCATTTTCTTTTTA | 18472 |
rs247297165 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74704915 | ACTACAGAGAAAGAA[C/T]AATAAATGGGACATA | 18472 |
rs247332245 | in-del | -/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74709873 | AAACTGCCATGTGGG[-/T]GCTGGTGAGATGGCT | 18472 |
rs247508556 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74721101 | CTTCATTAAACTTTT[A/C]AAAATATAGAATTGT | 18472 |
rs247564995 | snp | A/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74705818 | ATAGTGGTTTTTTTT[A/T]AAGATTATTATTAAG | 18472 |
rs247573015 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74708090 | AGACAGGGTTTCTCT[G/T]TATAGCCCTGGCTGT | 18472 |
rs247692816 | snp | C/G | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74689586 | TGTTGTCTACTCTAA[C/G]TTTGTCTGTGAAGAG | 18472 |
rs247744411 | snp | G/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74690793 | GAGATCCACCTGCCT[G/T]TGCCTCCTGAGGTGT | 18472 |
rs247778709 | in-del | -/AGAG | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74716027 | ACCTTACCTCTAAAT[-/AGAG]ATTTTTGTTCTATTT | 18472 |
rs247805796 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74702360 | GAGTACAGGTGTATT[C/T]CTAAATAAGCCATTT | 18472 |
rs247876653 | snp | A/C | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74716896 | TCATCATATGCTGCA[A/C]TGGCAAAGTGATGAT | 18472 |
rs247880663 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74676084 | TACTTAAAGGGATTT[-/A]TTAAAAAATCTATTA | 18472 |
rs248014390 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74704574 | TGTGTGTGTGTGTGT[G/T]TGTGTTTGTTTTTTG | 18472 |
rs248041643 | in-del | -/TAAAAAA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74682341 | CTTTTTTTAGTCTAT[-/TAAAAAA]AAAAAAAACATAAAA | 18472 |
rs248075404 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74694023 | AATGATTAAGAAAGA[C/T]ACCTAACAATTCACC | 18472 |
rs248119121 | snp | A/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74717714 | AGCACCTTTACTTTC[A/T]AAATACCCATCTACT | 18472 |
rs248129818 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74694917 | CTCGGACTCAACAGT[A/G]TTCCTGACTCCTGAG | 18472 |
rs248169081 | in-del | -/A | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74722663 | AACAACTGCTGTGGC[-/A]AAAATGAAGAGAGAA | 18472 |
rs248196547 | snp | C/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74706090 | CAACAATCATTCTAT[C/T]TCTAAAATAAATTCA | 18472 |
rs248207699 | in-del | -/TCCCCTCCTTTCCTTTC | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74684991 | TTTCCCTTTCCTTTT[-/TCCCCTCCTTTCCTTTC]CGTATTTTTTGGCTG | 18472 |
rs248221106 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74687832 | GTGCGCCACCACGCC[C/T]GGCCCAGATTTATAT | 18472 |
rs248279098 | snp | A/G | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74696406 | ACAACCATCTGTAAC[A/G]AGATCTGACGCCCTC | 18472 |
rs248306858 | in-del | -/ATTAAA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74703402 | TTACCAAGTACTGGG[-/ATTAAA]AGGCCATGCATAACT | 18472 |
rs248404528 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74678021 | TTATTAAATTCCACT[C/T]GATGTCACTAGTATC | 18472 |
rs248481882 | snp | A/G | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74689215 | AAGTTAAACAAAGTT[A/G]TGTTTTATAATATAT | 18472 |
rs248545897 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74676385 | GGGAGAACAAAGGAA[G/T]TGACTTTCTCTTAGA | 18472 |
rs248589811 | in-del | -/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74707326 | CACAACTGGTGTACC[-/T]TTATCTTTTGTTTTA | 18472 |
rs248626498 | snp | A/G/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74684143 | ATGGATGAATGTATG[A/G/T]ATGTATGTATGTATG | 18472 |
rs248658879 | in-del | -/AAAAA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74721056 | AAAAATGAACAAGTG[-/AAAAA]AAAAAAAAAAAGAAA | 18472 |
rs248695189 | in-del | -/GG | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74707278 | ACACACAGACACACA[-/GG]CACACACACAGACAC | 18472 |
rs248772149 | in-del | -/ACC | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74681288 | TGTGCTGCTGCTGCT[-/ACC]ACCACCACTTCCGAC | 18472 |
rs248778204 | snp | C/G | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74707297 | ACACACAGACACACA[C/G]ACACACACACACACA | 18472 |
rs248837164 | in-del | -/TA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74680077 | TTTTCACTATTTTTT[-/TA]AAGTATTATGTGCAT | 18472 |
rs248846992 | snp | A/T | | | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74725041 | TTATTATATTATGAA[A/T]TGTATATTGATGACA | 18472 |
rs249011657 | in-del | -/AA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74706715 | GTAAAAATCCTACAG[-/AA]AAAAAAAAAAAAATC | 18472 |
rs249317157 | in-del | -/A | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74714787 | TAACACATATGGTAT[-/A]AAAAAAAATACTCAG | 18472 |
rs249350578 | in-del | -/TTTGT | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74698374 | TTGTTTGTTTGTTTG[-/TTTGT]TTTTTTGAGACAGGC | 18472 |
rs249416620 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74705085 | TTATTCAACAGATAA[A/G]ACGTAATCCATATGA | 18472 |
rs249421553 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74717498 | TAATATTTGTGCTTT[A/G]TGGTATAAACATGTG | 18472 |
rs249448486 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74694759 | GATTAAAGGTGTGTA[C/T]CACCACAGCTTGGAA | 18472 |
rs249483591 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74704527 | CTCTTAAAAGCTGAG[C/T]CAACTCTCCAGCACT | 18472 |
rs249526387 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74681143 | ACAGAGATCCTCCTG[C/T]GTCTGCCTCTTGAGT | 18472 |
rs249548284 | snp | C/G | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74701795 | ATATCTTCACTAGCT[C/G]AAGTTAACTCCTGGC | 18472 |
rs249875236 | snp | A/T | | | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74726208 | AATCTTTAAAAGGTT[A/T]TGTCCAGAGTTTCAG | 18472 |
rs250039866 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74712861 | AAACTTAACTTAATA[A/C]ATTTTAAGAATACTT | 18472 |
rs250109729 | in-del | -/AAAAG | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74715497 | CTCGAAAAACCAAAA[-/AAAAG]AAAAAGAAAAAGAAA | 18472 |
rs250155471 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74712083 | CTTTTTGCTTTGGGT[G/T]TTTGTTTTATTTTGT | 18472 |
rs250156613 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74685056 | AGACCAGGCTGGTCT[C/T]GAACCACCTGGCTCT | 18472 |
rs250158400 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74698982 | GGGCACTGGTGACAC[A/G]CGCCTTTAATCCCAG | 18472 |
rs250193870 | in-del | -/CTGGTTGTAGACCAGGCAGG | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74719175 | TTTCTCTGTGTAACC[-/CTGGTTGTAGACCAGGCAGG]CTGGCCTCAAATTCT | 18472 |
rs250217993 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74686385 | GTGGACTGACTTAAG[A/G]TCTCAATTTTACTAG | 18472 |
rs250351221 | snp | G/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74690188 | ACACATTGAATAAAC[G/T]GACTTAAGAAGACCT | 18472 |
rs250500224 | in-del | -/TAAAA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74686077 | ACCTGTCAAGTGAAT[-/TAAAA]AAAAAAAAAAAATGG | 18472 |
rs250535536 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74679040 | cttctgaaggtcctc[C/T]tgagttcaaatccca | 18472 |
rs250660052 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74709172 | ATTTATTACAGGAAT[G/T]AGTAAAACCCATAAC | 18472 |
rs250701246 | in-del | -/A | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74694334 | AAGAACATCAAAAGT[-/A]AAAAAAATTTTTAAA | 18472 |
rs250721450 | in-del | -/GATT | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74708693 | GATGTGAGCTAAATG[-/GATT]TATTTATTATGTCTT | 18472 |
rs250778976 | in-del | -/CACAC | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74687157 | ACACACACACACACA[-/CACAC]ACAAAAATTTGGAGA | 18472 |
rs250807190 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74679918 | CTCTTTGCTTCCACC[G/T]TGGATGCCGGAATCA | 18472 |
rs250883734 | in-del | -/TT | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74693779 | AGTGGGGAAGAACAC[-/TT]GTGCAAATATGAAGA | 18472 |
rs250966742 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74700803 | GTGGTATATAAGTAT[A/T]CAGTGTCTGCATGTG | 18472 |
rs251001311 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74681553 | TTTCTAAAACTATGA[A/T]GTTATATTCTAAGAC | 18472 |
rs251027947 | snp | A/G | | | downstream-variant-500B | Pafah1b1 | Mm_Celera | 11:74673893 | CAAGTCTCACTTCCT[A/G]CCAAGATCAACACAA | 18472 |
rs251051163 | in-del | -/ACAG | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74707294 | CACACACACAGACAC[-/ACAG]ACACACACACACACA | 18472 |
rs251107890 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74715537 | AAAGAATGATGTGTG[C/T]ATGTGGGACCATATA | 18472 |
rs251193854 | in-del | -/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74714548 | GTTTAGCTCATATAA[-/T]TTTCCATCCTCATAA | 18472 |
rs251204970 | in-del | -/GCAT | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74712167 | ACTCAGGAGTCAGAA[-/GCAT]GCAGATTTTTGAGTC | 18472 |
rs251228466 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74714321 | AATTCTACTTCAATC[A/G]TCCAGTCAATAATCT | 18472 |
rs251251048 | in-del | -/AAAAAAA | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74690305 | GAAAAAGTAAGATTT[-/AAAAAAA]AAAAAAAAAAAAAAT | 18472 |
rs251265371 | snp | C/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74713691 | TCTTCCAGAGAACCT[C/G]TTTGATCTCCAGCAA | 18472 |
rs251283866 | in-del | -/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74709736 | ATACAAGTTATAAAC[-/T]TTTTTTTTAGTTTTT | 18472 |
rs251296622 | in-del | -/AA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74713839 | AAAATTTAAAAAAAG[-/AA]AAAAAAAAAAGAAAA | 18472 |
rs251618523 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74677177 | AAAGATTCTGAATTG[C/T]AGTCTTATTATCTAA | 18472 |
rs251647033 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74707689 | TAGAAAGGAGGGCAC[C/T]GAGTTGAAGGGTGTT | 18472 |
rs251650536 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74719467 | CAGGGCTAGTTCAGT[A/G]ATGGGTAACACCCAA | 18472 |
rs251699493 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74694991 | TTTTCTTGAACCTAT[G/T]AATTTTCCTTACAGA | 18472 |
rs251704771 | in-del | -/GAGGG | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74708021 | TCCCCCACAGAGAGA[-/GAGGG]GGGGGGAAGGTTTTG | 18472 |
rs251725668 | snp | C/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74717092 | GAAGCAAAACACTAA[C/G]ATCTGAGCTTGCTCA | 18472 |
rs251749500 | in-del | -/ACCAA | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74720676 | AGGGCTTAAAAATAT[-/ACCAA]ACACTACTAAAAGTG | 18472 |
rs251784599 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74718012 | AGAATCCCTGACAGA[G/T]TAGTCCTGTTTTAAC | 18472 |
rs252006160 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74685815 | ACTAGGAATTAAATG[C/T]AGGGTACCTAAACAT | 18472 |
rs252169892 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74679722 | AAGGCCTTATAACCT[C/T]GAACTTCAGGCAGGC | 18472 |
rs252188202 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74703744 | ttgcacccacatggc[A/G]gctcacaagcacctg | 18472 |
rs252200773 | in-del | -/A | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74682928 | ATAGGTAAATAAAAT[-/A]AAAAATAAATTAAAA | 18472 |
rs252235403 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74680333 | TAATAATTAAAAATT[A/G]TGGAGCCAAAGAGAT | 18472 |
rs252317244 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74720750 | CTAAGGTAGAAAAAA[G/T]GCAGTTAGAGGACTG | 18472 |
rs252406297 | in-del | -/AAA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74721723 | GATGTTCATCAAGAG[-/AAA]AAAAAAAAACTATTT | 18472 |
rs252406857 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74722793 | GCTAAAATGACCTTT[A/C]TGTTACTGGATCTTT | 18472 |
rs252461439 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74682790 | TAATGAACAAACAAA[A/C]GATTAATTTAGAGCC | 18472 |
rs252554501 | snp | C/G | | | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74724529 | TGTACCCGAGCCGAC[C/G]GGCGAGCTTGCGTCC | 18472 |
rs252584012 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74695190 | GTGTCACAATGCTTA[A/G]CTAATTGAACAATTT | 18472 |
rs252584671 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74680880 | CAAACAAACAAAAAA[C/T]AGGGCAGCAACAACA | 18472 |
rs252622941 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74681632 | AAAGAATGTCTAATA[G/T]CCACCTCCCTCTTAC | 18472 |
rs252631077 | in-del | -/AA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74694256 | ACTTATACACATATT[-/AA]AAAAAGATTAAAAAT | 18472 |
rs252638736 | in-del | -/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74688224 | CCAGAATTTTTTTTT[-/G]TTTTTTGTTTTTTGT | 18472 |
rs252716956 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74716499 | TGATGCGTCTGAAGA[C/T]AGCCACAGTGTACTT | 18472 |
rs253126688 | snp | C/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74709058 | TAAATTCCAGAAGGT[C/G]AGAAGTGACAAAGAC | 18472 |
rs253148507 | in-del | -/CC | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74710518 | GAGCCATCTCTCCAG[-/CC]CCCTTTTTTTTTTTA | 18472 |
rs253254161 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74708052 | TTTGTTTTTGGTTTT[G/T]TTTTTTTGTTTTTGG | 18472 |
rs253286735 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74703973 | TTAACTTCATAAGTC[A/G]TTTTGAACCTCTGAC | 18472 |
rs253341694 | in-del | -/ATAG | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74712751 | GATCTACAGGTTTAC[-/ATAG]ATAGTGAGTTCCAGT | 18472 |
rs253373198 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74712599 | CCAGCCTCTGTGGAC[A/T]CCTGCATTCACATGT | 18472 |
rs253403326 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74680112 | GTTGTGCCTATATGT[A/G]TGCCTGTACGACACG | 18472 |
rs253446126 | in-del | -/ATA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74692940 | ATCCACCTAAAACCT[-/ATA]ATGTTTTTAGATTCT | 18472 |
rs253484122 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74700945 | TGGCTGCATTCAGCA[C/T]GAAGTTCACTGATAA | 18472 |
rs253532332 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74693732 | CCAGATTCAGTTAAA[A/G]GATCCTGTGTCTCAC | 18472 |
rs253549833 | in-del | -/AAAAAAAAAA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74721246 | AGAAACCCTGCCTCC[-/AAAAAAAAAA]AAAAAAAAAAAAAAA | 18472 |
rs253570391 | in-del | -/T | | | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74724905 | TTTAATCGGAAGGAA[-/T]TCGCCTGTAGATGTG | 18472 |
rs253577783 | in-del | -/AAAAG | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74714162 | GAAAATATCCAATTT[-/AAAAG]AAAAGAAAAGAAAGA | 18472 |
rs253619293 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74721811 | GTAGCCAAATATCCC[C/T]AGCATTCATTAATTT | 18472 |
rs253659211 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74713580 | CAGCCTGGATTTCTA[A/G]TTGCCAGGAAAAATG | 18472 |
rs253738078 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74702635 | TATTATCAATCACTT[A/G]ATGTGACCTTTCACT | 18472 |
rs253790903 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74704105 | CAGAGAAAGTATTTT[A/T]AAAAAAAGAAGACAA | 18472 |
rs253816878 | in-del | -/TG | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74698814 | AACCACACACACACA[-/TG]CACGTATGCATGTAT | 18472 |
rs253934238 | in-del | -/AAATGAAACCAAAATAAACAGATCCCAGAAGACAAAAAAATATATATAAAT | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74687495 | AACCATGTCTCAAAA[lengthTooLong]AAATGAAACCAAAAT | 18472 |
rs254021193 | snp | C/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74685551 | ATGGACACTTAGATA[C/G]TGCAGCACCGAACTC | 18472 |
rs254077493 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74687190 | GAAATAGATAATATT[A/T]TAAAAAAATGCCTAG | 18472 |
rs254190274 | snp | A/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74690305 | AGAAAAAGTAAGATT[A/T]AAAAAAAAAAAAAAT | 18472 |
rs254343536 | in-del | -/ACAC | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74707306 | CACACAGACACACAC[-/ACAC]ACACAACTGGTGTAC | 18472 |
rs254344936 | in-del | -/AATT | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74714446 | AAATATGTGATACAC[-/AATT]AATCAGAATGCTTGC | 18472 |
rs254353632 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74678616 | GCCCTATTTCTTTTT[C/T]TCCCCCCTCCAAACA | 18472 |
rs254426178 | in-del | -/TTTTGTTTTG | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74696797 | GTTTTTTTGTTTCTT[-/TTTTGTTTTG]TTTTGTTTTTTTTAA | 18472 |
rs254445946 | in-del | -/ACACAC | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74719961 | TAATTCACACAAAGA[-/ACACAC]ACACACACACACAAA | 18472 |
rs254626207 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74692632 | CTGCCATATCTCTGA[A/G]CGTTGGGATTAAAGA | 18472 |
rs254763962 | in-del | -/TTTTTA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74678971 | AGGTTGAAAACTTTT[-/TTTTTA]AAGATTTCTTTTAGA | 18472 |
rs254912418 | in-del | -/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74678302 | ATAGTGGATAGTGCA[-/T]TTTTTTTTTCCTTTC | 18472 |
rs254978623 | snp | C/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74688803 | ACCTTACTTTAATCA[C/T]ATCATTTACTAGGCA | 18472 |
rs254996235 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74713045 | gattacaaacaccac[C/T]atttctgacCAGTCC | 18472 |
rs255096243 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74716428 | ATCCTGAGTTCAAAT[C/T]CCAGCAACCACATGG | 18472 |
rs255276639 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74703087 | CTCATGCCTTAGGCA[A/G]GCAGAAGCAAGCAGA | 18472 |
rs255284298 | in-del | -/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74687647 | AGATACAGATTTATC[-/T]TTTTTTTGGGGGGGT | 18472 |
rs255368474 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74692797 | GCCAATGTAAGGCAC[C/T]AGAAATCAAATCCAA | 18472 |
rs255495496 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74705177 | AAAAGACAGAAGCAG[A/G]TGGATTATCTGTGAG | 18472 |
rs255558007 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74702445 | CCAGCCTGGGTTTTT[C/T]CCCTCCACCAAGAAT | 18472 |
rs255687870 | snp | A/C | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74715253 | AAAAAAAAAAGAAAA[A/C]CCAACCATCTGTCAT | 18472 |
rs255755374 | in-del | -/A | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74686078 | ACCTGTCAAGTGAAT[-/A]AAAAAAAAAAATGGT | 18472 |
rs255892487 | in-del | -/TAA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74698589 | CTGACTTTTTTTTTT[-/TAA]AAATTAGAAGAGCTA | 18472 |
rs255901931 | snp | C/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74678458 | TTTGTCTGCCTGTCT[C/G]TGTGTGTGTGTATAA | 18472 |
rs255914130 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74715526 | aagaaaaagaaaaag[A/G]aTGAtgtgtgtatgt | 18472 |
rs255968941 | snp | A/C | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74689943 | AGGGGTGCAGTGCAA[A/C]ACACAATGAGAAGCA | 18472 |
rs256028969 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74677795 | CTAAGCCAGACAGAA[C/T]GCTTTGCTTGCTTTT | 18472 |
rs256070325 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74680920 | CATATATTTTTGTGG[C/T]CACACCAAAAGGAAG | 18472 |
rs256149817 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74712865 | TTAACTTAATAAATT[G/T]TAAGAATACTTATGA | 18472 |
rs256162753 | in-del | -/A | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74721851 | TTGGCTAGAATAATT[-/A]AAAAAAAAAAACTAG | 18472 |
rs256345312 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74696159 | TTCCGTATTTCCACT[G/T]TTGGGGAATCTAAGT | 18472 |
rs256357387 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74722869 | AGAAAAGCAGTAATT[C/T]TATTTTCTCCCAATT | 18472 |
rs256481040 | snp | C/T | | | intron-variant, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74723684 | GGCAGGAGGGCGATG[C/T]CGCCCGAGAGGCCAC | 18472 |
rs256528335 | in-del | -/TTTTT | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74708046 | AAGGTTTTGTTTTTG[-/TTTTT]GTTTTGTTTTTTTGT | 18472 |
rs256620638 | in-del | -/GGGG | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74714100 | ATGGGATAGGGGTTT[-/GGGG]GGGGGGGGACTGGAA | 18472 |
rs256632041 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74687162 | CACACACACACACAC[A/C]CAAAAATTTGGAGAA | 18472 |
rs256771674 | in-del | -/CATT | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74696813 | TTTGTTTTTTTTAAA[-/CATT]GATTAATTGATTGAT | 18472 |
rs256852462 | snp | C/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74694927 | ACAGTATTCCTGACT[C/G]CTGAGCACTGAATAT | 18472 |
rs256897524 | snp | A/C | | | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74725734 | GAATTCCAGGACAGA[A/C]AACTACATAGAGAAA | 18472 |
rs257090947 | snp | A/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74709777 | ACTTTTATTTTATGT[A/C]CATTGGTAGTTTGCC | 18472 |
rs257099993 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74695832 | ACATGCAGGGAACAT[A/G]AAATCTCTTTGAACT | 18472 |
rs257161602 | snp | C/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74682491 | GCTGTACCTAGCCTA[C/G]AAAGAAAGATAGGCT | 18472 |
rs257184067 | snp | C/T | | | upstream-variant-2KB | Pafah1b1 | Mm_Celera | 11:74725577 | GCAGGAGACTTGCCA[C/T]GAGTTTGAAGCCAGC | 18472 |
rs257241803 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74687297 | ATGGCTAAGCCATCT[G/T]CTCCAGCCCACATTT | 18472 |
rs257310007 | snp | A/C | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74683984 | CCCAGATAAGAAAAA[A/C]AAAACAAAAAAAAAA | 18472 |
rs257408790 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74698023 | TAATAAATAAATAAA[C/T]CTAAAAAACAAAACA | 18472 |
rs257410297 | in-del | -/AA | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74689379 | TCATTTACATTTATT[-/AA]TAAAGATGATCATAA | 18472 |
rs257416950 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74705298 | GGAGGAAGAGGAAGA[A/G]GAGAGAGAGAAAGAA | 18472 |
rs257447275 | in-del | -/TT | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74681166 | CTTGAGTATTGGGAA[-/TT]TTTTTTTTCCGTGTT | 18472 |
rs257463766 | in-del | -/TTTTTTT | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74688215 | TGTGCCCAGCCAGAA[-/TTTTTTT]TTGTTTTTTGTTTTT | 18472 |
rs257542354 | in-del | -/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74694592 | GCATAACTAAACACA[-/G]GAAGATTTTGACAGC | 18472 |
rs257606097 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74708022 | CCCCCACAGAGAGAG[A/G]GGGGGGGGGAAGGTT | 18472 |
rs257703589 | in-del | -/C | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74706688 | TGGCATGTATCAGAA[-/C]AATACAGTGATTGTA | 18472 |
rs257714425 | in-del | -/TT | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74698579 | CCTGGTAAAACTGAC[-/TT]TTTTTTTTTTAAATT | 18472 |
rs257825738 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74703434 | CCAACTAGCCAAAGA[A/T]CTGTATTCGTAAATA | 18472 |
rs257857002 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74677124 | CAAAGGGGTCATGAC[-/A]AAAACTTCATGTGTA | 18472 |
rs257970678 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74676125 | TAAAATGCAGTCCAG[-/A]AAAAAAAAATTATCA | 18472 |
rs258073924 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74695143 | GAGAAACCCTGTCTC[A/G]AAAAACCAAAAAAAA | 18472 |
rs258410553 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74692287 | TTTAAAGGCAGCAAA[G/T]CTGAAGTGGCTTGAA | 18472 |
rs258416058 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74717532 | ACTAAGTATTTGTAA[A/T]TTTTTTTTTCAAAAG | 18472 |
rs258443180 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74683279 | TTGAGCCATCTTACT[A/G]GCCCAATAATAACTG | 18472 |
rs258445436 | in-del | -/CAGGAA | | | utr-variant-3-prime, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74675509 | GCAGGGGAGGAAACC[-/CAGGAA]CAGCAGCTTTGCTCC | 18472 |
rs258545663 | in-del | -/AAA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74712447 | AATGTATTATATAAT[-/AAA]AAACAAAATGATGTT | 18472 |
rs258585581 | in-del | -/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74705268 | AACAAAAAAGGAGGA[-/G]GGGGGGGAGAAGGAG | 18472 |
rs258586423 | snp | A/T | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74688372 | ATCATATATTCAAGC[A/T]TATCTACATGAAAGC | 18472 |
rs258613594 | in-del | -/AAA | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74721850 | TTGGCTAGAATAATT[-/AAA]AAAAAAAAAAAACTA | 18472 |
rs258647894 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74681175 | TTGGGAATTTTTTTT[C/T]CGTGTTTGTTCTTGT | 18472 |
rs258669118 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74718549 | TAATAAATAAATCTT[A/T]AAAAAAAAACACAAA | 18472 |
rs258685031 | snp | A/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74692180 | AGAGTGAGTCCTAGG[A/T]CAGCTAGGGCTAAAG | 18472 |
rs258710573 | in-del | -/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74694342 | TCAAAAGTAAAAAAA[-/T]TTTTAAAAAAGGAAG | 18472 |
rs258777817 | in-del | -/A | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74682342 | TTTTTTTAGTCTATT[-/A]AAAAAAAAAAAAACA | 18472 |
rs258982557 | snp | A/G | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74720948 | AGTGGATAAAGATGT[A/G]TGCCACTAAATCTGA | 18472 |
rs259089893 | in-del | -/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74686659 | CATTCTTAGAAGACA[-/T]TTTTTTTTCCTTTTC | 18472 |
rs259171529 | snp | A/G | | | intron-variant | Pafah1b1 | GRCm38.p3 | 11:74705832 | TTAAGATTATTATTA[A/G]GGTCATGTCCTGTAA | 18472 |
rs259181170 | snp | G/T | | | intron-variant, nc-transcript-variant | Pafah1b1 | Mm_Celera | 11:74723670 | TGCTAAGTCACGGCG[G/T]CAGGAGGGCGATGCC | 18472 |
rs259303647 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74680138 | ACACGCTGAATGCAG[G/T]GCTCTCAGCAGCCCA | 18472 |
rs259309890 | snp | C/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74680508 | ACAAAAAGAGCACAC[C/T]GGGGAGTAGAGGCGC | 18472 |
rs259335833 | snp | G/T | | | intron-variant | Pafah1b1 | Mm_Celera | 11:74704487 | CTGGGAATCAAACAC[G/T]AGTCCTAAGCAGGAG | 18472 |