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 |